{"curie": "MONDO:0002154", "names": ["Trich", "trichomona", "trichomonas", "Trichomonosis", "trichomonosis", "trichomoniasis", "Trichomoniases", "Trichomoniasis", "TRICHOMONIASIS", "TRICHOMONAL INFECTION", "Trichomonas Infection", "trichomonas infection", "Trichomonas infection", "Trichomonas; infection", "Trichomonas Infections", "infection; Trichomonas", "Trichomonas infections", "Infection, Trichomonas", "Infections, Trichomonas", "infections, Trichomonas", "Infection by Trichomonas", "Trichomoniasis (diagnosis)", "Trichomoniasis, unspecified", "Infection by Trichomonas, NOS", "Disease due to Trichomonadidae", "Infection caused by Trichomonas", "DISEASES DUE TO TRICHOMONADIDAE", "Disease caused by Trichomonadidae", "Infection caused by Trichomonas (disorder)", "Disease caused by Trichomonadidae (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichomoniasis", "shortest_name_length": 5}
{"curie": "UMLS:C5555184", "names": ["Refractory Ovarian Transitional Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Ovarian Transitional Cell Carcinoma", "shortest_name_length": 46}
{"curie": "MONDO:0012263", "names": ["AIS4", "VAMAS5", "autoimmune disease, susceptibility to, 4", "AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 4", "AUTOIMMUNE DISEASE SUSCEPTIBILITY LOCUS, CHROMOSOME 4-RELATED", "autoimmune disease susceptibility locus, chromosome 4-related", "vitiligo-associated multiple autoimmune disease susceptibility 5", "VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune disease, susceptibility to, 4", "shortest_name_length": 4}
{"curie": "UMLS:C0396009", "names": ["Pharyngeal Fistula", "pharyngeal fistula", "Pharyngeal fistula", "Pharyngocutaneous fistula", "Pharyngocutaneous Fistula", "pharyngocutaneous fistula", "pharyngeal fistula (diagnosis)", "Pharyngocutaneous fistula (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pharyngocutaneous fistula", "shortest_name_length": 18}
{"curie": "MONDO:0002376", "names": ["spleen angiosarcoma", "Splenic Angiosarcoma", "splenic angiosarcoma", "Angiosarcoma of Spleen", "Angiosarcoma of spleen", "angiosarcoma of spleen", "Splenic Hemangiosarcoma", "splenic hemangiosarcoma", "Splenic hemangiosarcoma", "hemangiosarcoma of spleen", "Hemangiosarcoma of Spleen", "Hemangiosarcoma of spleen", "Angiosarcoma of the Spleen", "angiosarcoma of the spleen", "spleen angiosarcoma (disease)", "Hemangiosarcoma of the Spleen", "hemangiosarcoma of the spleen", "angiosarcoma (disease) of spleen", "Angiosarcoma of spleen (disorder)", "angiosarcoma of spleen (diagnosis)", "Hemangiosarcoma of spleen (disorder)", "hemangiosarcoma of spleen (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spleen angiosarcoma", "shortest_name_length": 19}
{"curie": "MONDO:0004747", "names": ["Harelip", "harelip", "HARELIP", "Hare lip", "Harelips", "hare lip", "Cleft Lip", "LIP CLEFT", "cleft lip", "Cleft lip", "Lip cleft", "CLEFT LIP", "cleft; lip", "Cleft Lips", "lip; cleft", "Lip, Cleft", "Lips, Cleft", "Cleft lip NOS", "cheiloschisis", "Cheiloschisis", "CL - Cleft lip", "Cleft lip, NOS", "Cleft upper lip", "labium leporinum", "Labium leporinum", "Cleft of upper lip", "cleft lip (disease)", "Cleft lip (disorder)", "cleft lip (diagnosis)", "Cleft lip, unspecified", "lip; fissure, congenital", "Congenital fissure of lip", "congenital fissure of lip", "Cheiloschisis of upper lip", "cleft lip (physical finding)", "Unilateral complete cleft lip", "complete unilateral cleft lip", "Complete unilateral cleft lip", "cleft lip, unilateral, complete", "Cleft lip, unilateral, complete", "complete unilateral cleft lip (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleft lip", "shortest_name_length": 7}
{"curie": "MONDO:0000412", "names": ["neonatal period electroclinical syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal period electroclinical syndrome", "shortest_name_length": 40}
{"curie": "MONDO:0004741", "names": ["tyrosinemia", "Tyrosinemia", "Tyrosinemias", "tyrosinaemia", "Tyrosinaemia", "Hypertyrosinemia", "Hereditary tyrosinemia", "Hereditary Tyrosinemia", "Tyrosinemia (disorder)", "hereditary tyrosinemia", "tyrosinemia (diagnosis)", "Tyrosinemia, Hereditary", "Hereditary tyrosinaemia", "Hereditary Tyrosinemias", "Tyrosinemias, Hereditary", "Hereditary hypertyrosinemia", "Hereditary hypertyrosinaemia", "Hereditary hypertyrosinemia, NOS", "Hereditary hypertyrosinemia (disorder)", "Tyrosinemia-tyrosiluria hereditary syndrome", "Tyrosinaemia-tyrosiluria hereditary syndrome", "Tyrosinemia-tyrosiluria, hereditary syndrome", "Tyrosinemia-tyrosiluria hereditary syndrome, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tyrosinemia", "shortest_name_length": 11}
{"curie": "MONDO:0019567", "names": ["EDS I", "EDSCL1", "EDS1, FORMERLY", "EDS I, FORMERLY", "Ehlers-Danlos syndrome type 1", "type I Ehlers-Danlos syndrome", "Ehlers-Danlos syndrome type I", "Ehlers-Danlos syndrome, type 1", "Ehlers-Danlos Syndrome, Type I", "Ehlers-Danlos syndrome, gravis", "Ehlers-Danlos syndrome, type I", "Cutis hyperelastica I, gravis type", "Ehlers-Danlos syndrome, Gravis type", "Ehlers-Danlos syndrome classic type 1", "EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 1", "Ehlers-Danlos syndrome, classic type, 1", "EHLERS-DANLOS SYNDROME, TYPE I, FORMERLY", "Ehlers-Danlos syndrome, type 1 (disorder)", "Ehlers-Danlos Syndrome, Severe Classic Type", "Ehlers-Danlos syndrome, severe classic form", "Ehlers-Danlos syndrome, classic severe form", "EHLERS-DANLOS SYNDROME, GRAVIS TYPE, FORMERLY", "EHLERS-DANLOS SYNDROME, SEVERE CLASSIC TYPE, FORMERLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ehlers-Danlos syndrome, classic type, 1", "shortest_name_length": 5}
{"curie": "UMLS:C5446419", "names": ["Unresectable Malignant Gastric Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Malignant Gastric Neoplasm", "shortest_name_length": 39}
{"curie": "MONDO:0033622", "names": ["SPGF44", "spermatogenic failure 44", "SPERMATOGENIC FAILURE 44"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 44", "shortest_name_length": 6}
{"curie": "UMLS:C0278485", "names": ["Breast cancer stage I", "stage i breast cancer", "breast cancer stage i", "stage I breast cancer", "Stage I Breast Cancer", "breast cancer, stage I", "Carcinoma breast stage I", "Breast carcinoma stage I", "Breast cancer NOS stage I", "Breast carcinoma NOS stage I", "Stage I Breast Cancer AJCC v6", "Breast Cancer Stage I AJCC v6", "Breast Carcinoma Stage I AJCC v6", "Stage I Breast Carcinoma AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carcinoma breast stage I", "shortest_name_length": 21}
{"curie": "UMLS:C4288005", "names": ["Vulvar Lipoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Lipoma", "shortest_name_length": 13}
{"curie": "MESH:D001169", "names": ["Arthritis, Experimental"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arthritis, Experimental", "shortest_name_length": 23}
{"curie": "MONDO:0013658", "names": ["MRD11", "CHROMOSOME 20q11-q12 DELETION SYNDROME", "autosomal dominant mental retardation 11", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 11", "mental retardation, autosomal dominant 11", "autosomal dominant intellectual disability 11", "intellectual disability, autosomal dominant 11", "mental retardation, autosomal dominant type 11", "intellectual disability, autosomal dominant type 11", "autosomal dominant intellectual developmental disorder 11", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 11", "intellectual developmental disorder, autosomal dominant 11", "autosomal dominant non-syndromic intellectual disability 11", "EPB41L1 autosomal dominant non-syndromic intellectual disability", "autosomal dominant non-syndromic intellectual disability caused by mutation in EPB41L1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 11", "shortest_name_length": 5}
{"curie": "UMLS:C1960924", "names": ["Right-sided Staphylococcus aureus endocarditis", "Right-sided Staphylococcus aureus endocarditis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Right-sided Staphylococcus aureus endocarditis", "shortest_name_length": 46}
{"curie": "MONDO:0009520", "names": ["HMGCLD", "HL DEFICIENCY", "HL deficiency", "Hmgcl deficiency", "HMGCL DEFICIENCY", "HMG CoA Lyase Deficiency", "HMG-CoA Lyase Deficiency", "HMG CoA lyase deficiency", "HMG-CoA lyase deficiency", "HMG-CoA LYASE DEFICIENCY", "HMG-Coa lyase deficiency", "defect in leucine metabolism", "Hydroxymethylglutaric aciduria", "HYDROXYMETHYLGLUTARIC ACIDURIA", "Hydroxymethylglutaric Aciduria", "3-OH 3-Methyl Glutaric Aciduria", "3-OH 3-Methyl glutaric aciduria", "3-Hydroxy-3-methylglutaric aciduria", "3-Hydroxy-3-Methylglutaric Aciduria", "3-hydroxy-3-methylglutaric aciduria", "3-Hydroxy 3-Methyl Glutaric Aciduria", "3-Hydroxyl 3-Methyl Glutaric Aciduria", "Hydroxymethylglutaric aciduria (disorder)", "hydroxymethylglutaryl-CoA lyase deficiency", "Hydroxymethylglutaryl-CoA lyase deficiency", "Hydroxymethylglutaryl-CoA Lyase Deficiency", "Hydroxymethylglutaryl CoA lyase deficiency", "Deficiency of Hydroxymethylglutaryl-CoA Lyase", "deficiency of hydroxymethylglutaryl-CoA lyase", "Deficiency of hydroxymethylglutaryl-CoA lyase", "3-HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY", "3-hydroxy-3-methylglutaryl-CoA lyase deficiency", "3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency", "3-Hydroxy-3-methylglutaryl-CoA lyase deficiency", "3-Hydroxy-3-Methylglutaryl-Coenzyme A Lyase Deficiency", "Deficiency of hydroxymethylglutaryl-CoA lyase (disorder)", "3-hydroxy-3-methylglutaryl-CoA lyase deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "3-hydroxy-3-methylglutaric aciduria", "shortest_name_length": 6}
{"curie": "MONDO:0014014", "names": ["EBNS", "EBS4", "EBS-AR exophilin 5", "epidermolysis bullosa, nonspecific, autosomal recessive", "epidermolysis bullosa simplex due to exophilin 5 deficiency", "EPIDERMOLYSIS BULLOSA SIMPLEX 4, LOCALIZED OR GENERALIZED INTERMEDIATE, AUTOSOMAL RECESSIVE", "epidermolysis bullosa simplex 4, localized or generalized intermediate, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolysis bullosa simplex 4, localized or generalized intermediate, autosomal recessive", "shortest_name_length": 4}
{"curie": "MONDO:0014271", "names": ["CDGIx", "CDG1X", "CDG Ix", "CDG-Ix", "CDG IX", "STT3B-CDG", "CDG syndrome type Ix", "CDG syndrome type IX", "congenital disorder of glycosylation Ix", "congenital disorder of glycosylation 1x", "STT3B-congenital disorder of glycosylation", "congenital disorder of glycosylation type IX", "Congenital disorder of glycosylation type Ix", "Congenital disorder of glycosylation type 1x", "Congenital disorder of glycosylation type 1X", "congenital disorder of glycosylation type 1x", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ix", "congenital disorder of glycosylation, type IX", "STT3B-CDG (congenital disorder of glycosylation)", "carbohydrate deficient glycoprotein syndrome type IX", "Carbohydrate deficient glycoprotein syndrome type Ix", "Congenital disorder of glycosylation type 1x (disorder)", "Congenital disorder of glycosylation type 1x (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "STT3B-congenital disorder of glycosylation", "shortest_name_length": 5}
{"curie": "UMLS:C5555522", "names": ["Cancer-Associated Anorexia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cancer-Associated Anorexia", "shortest_name_length": 26}
{"curie": "UMLS:C4683666", "names": ["Nodal Marginal Zone Lymphoma by Ann Arbor Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nodal Marginal Zone Lymphoma by Ann Arbor Stage", "shortest_name_length": 47}
{"curie": "MONDO:0016710", "names": ["MBEN", "Nodular Medulloblastoma", "nodular medulloblastoma", "cerebellar neuroblastoma", "Cerebellar Neuroblastoma", "medulloblastoma with extensive nodularity", "Medulloblastoma with Extensive Nodularity", "Medulloblastoma with extensive nodularity", "Medulloblastoma with extensive nodularity (morphologic abnormality)", "medulloblastoma with extensive nodularity and advanced neuronal differentiation", "Medulloblastoma with Extensive Nodularity and Advanced Neuronal Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "medulloblastoma with extensive nodularity", "shortest_name_length": 4}
{"curie": "UMLS:C0347632", "names": ["Bruised liver", "contusion liver", "liver contusion", "Liver Contusion", "Liver contusion", "hepatic contusion", "Contusion of liver", "hepatic contusion (diagnosis)", "Contusion of liver (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Contusion of liver", "shortest_name_length": 13}
{"curie": "MONDO:0002192", "names": ["Vulval angiokeratoma", "vulvar angiokeratoma", "Vulvar Angiokeratoma", "Angiokeratoma of vulva", "mammalian vulva angiokeratoma", "Fordyce angiokeratoma of vulva", "angiokeratoma of mammalian vulva", "Angiokeratoma of vulva (disorder)", "mammalian vulva angiokeratoma of Fordyce", "angiokeratoma of Fordyce of mammalian vulva"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar angiokeratoma", "shortest_name_length": 20}
{"curie": "UMLS:C1518740", "names": ["Ovarian Steroid Cell Tumor, NOS", "Ovarian Steroid Cell Tumor, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Steroid Cell Tumor, Not Otherwise Specified", "shortest_name_length": 31}
{"curie": "UMLS:C1541469", "names": ["Recurrent Grade III Lymphomatoid Granulomatosis", "recurrent adult grade III lymphomatoid granulomatosis", "Recurrent Adult Grade III Lymphomatoid Granulomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Adult Grade III Lymphomatoid Granulomatosis", "shortest_name_length": 47}
{"curie": "MONDO:0012313", "names": ["SQT2", "short QT syndrome 2", "SHORT QT SYNDROME 2", "Short QT Syndrome 2", "KCNQ1 short QT syndrome", "short QT syndrome type 2", "short QT syndrome caused by mutation in KCNQ1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short QT syndrome type 2", "shortest_name_length": 4}
{"curie": "MONDO:0019874", "names": ["trisomy 7pter", "Trisomy 7pter", "Distal trisomy 7p", "distal trisomy 7p", "Distal duplication 7p", "distal duplication 7p", "distal trisomy type 7p", "telomeric duplication 7p", "Telomeric duplication 7p", "Distal trisomy 7p syndrome", "Distal trisomy 7p (diagnosis)", "partial trisomy chromosome 7p distal", "Distal trisomy 7p syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal trisomy 7p", "shortest_name_length": 13}
{"curie": "MONDO:0017364", "names": ["PEP syndrome", "poem syndrome", "POEMS syndrome", "POEMS Syndrome", "poems syndrome", "Syndrome, POEMS", "Takatsuki Syndrome", "Takatsuki syndrome", "Crow Fukase Syndrome", "Crow-Fukase Syndrome", "crow-fukase syndrome", "Takatsuki's Syndrome", "Crow-Fukase syndrome", "Syndrome, Crow-Fukase", "Syndrome, Takatsuki's", "Osteosclerotic myeloma", "osteosclerotic myeloma", "POEMS syndrome (diagnosis)", "polyneuropathy organomegaly", "Polyneuropathy Organomegaly", "Organomegaly, Polyneuropathy", "Polyneuropathy Organomegalies", "Organomegalies, Polyneuropathy", "polyneuropathy-endocrinopathy-plasma cell dyscrasia syndrome", "Polyneuropathy-endocrinopathy-plasma cell dyscrasia syndrome", "Polyneuropathy, organomegaly, endocrinopathy, M-protein, and skin changes", "POEMS - Polyneuropathy organomegaly endocrinopathy monoclonal and skin changes", "Polyneuropathy organomegaly endocrinopathy monoclonal gammopathy and skin changes", "Polyneuropathy, Organomegaly, Endocrinopathy, M Protein, and Skin Changes Syndrome", "polyneuropathy, organomegaly, endocrinopathy, M protein, and skin changes syndrome", "Polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes syndrome", "Polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes (POEMS) syndrome", "Polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "POEMS syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0007589", "names": ["EVR1", "FEVR, Autosomal Dominant", "FEVR, autosomal dominant", "FEVR, AUTOSOMAL DOMINANT", "CRISWICK-SCHEPENS SYNDROME", "retinopathy of prematurity", "Criswick-Schepens syndrome", "Exudative Vitreoretinopathy 1", "exudative vitreoretinopathy 1", "Exudative vitreoretinopathy 1", "EXUDATIVE VITREORETINOPATHY 1", "exudative vitreoretinopathy type 1", "EXUDATIVE VITREORETINOPATHY, FAMILIAL, AUTOSOMAL DOMINANT", "Exudative vitreoretinopathy, familial, autosomal dominant", "exudative vitreoretinopathy, familial, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exudative vitreoretinopathy 1", "shortest_name_length": 4}
{"curie": "MONDO:0032926", "names": ["SANDSTEF", "SANDESTIG-STEFANOVA SYNDROME", "Sandestig-Stefanova syndrome", "sandestig-stefanova syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sandestig-stefanova syndrome", "shortest_name_length": 8}
{"curie": "MONDO:0001114", "names": ["Septic myocarditis", "septic myocarditis", "Myocarditis septic", "septic; myocarditis", "myocarditis; septic", "Bacterial Myocarditis", "Bacterial myocarditis", "Myocarditis bacterial", "bacterial myocarditis", "myocarditis; bacterial", "bacterial; myocarditis", "Septic myocarditis, NOS", "Bacterial myocarditis, NOS", "septic myocarditis (diagnosis)", "Bacterial myocarditis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bacterial myocarditis", "shortest_name_length": 18}
{"curie": "MONDO:0008045", "names": ["SMAPME", "SMA-PME", "Jankovic Rivera syndrome", "Jankovic-Rivera syndrome", "myoclonus hereditary progressive distal muscular atrophy", "spinal muscular atrophy with progressive myoclonic epilepsy", "Spinal muscular atrophy with progressive myoclonic epilepsy", "SPINAL MUSCULAR ATROPHY WITH PROGRESSIVE MYOCLONIC EPILEPSY", "hereditary myoclonus and progressive distal muscular atrophy", "Hereditary myoclonus and progressive distal muscular atrophy", "Hereditary myoclonus with progressive distal muscular atrophy", "myoclonus, hereditary, with progressive distal muscular atrophy", "Spinal muscular atrophy-progressive myoclonic epilepsy syndrome", "spinal muscular atrophy-progressive myoclonic epilepsy syndrome", "MYOCLONUS, HEREDITARY, WITH PROGRESSIVE DISTAL MUSCULAR ATROPHY", "Myoclonus, Hereditary, with Progressive Distal Muscular Atrophy", "hereditary myoclonus-progressive distal muscular atrophy syndrome", "Hereditary myoclonus-progressive distal muscular atrophy syndrome", "Spinal muscular atrophy with progressive myoclonic epilepsy (disorder)", "spinal muscular atrophy with progressive myoclonic epilepsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal muscular atrophy-progressive myoclonic epilepsy syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C2826601", "names": ["Duodenal Extraskeletal Osteosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Duodenal Extraskeletal Osteosarcoma", "shortest_name_length": 35}
{"curie": "UMLS:C3275069", "names": ["CHRONIC TOTAL OCCLUSION", "Chronic Total Occlusion Vessel"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic Total Occlusion Vessel", "shortest_name_length": 23}
{"curie": "MONDO:0006372", "names": ["PTCY", "Pituicytoma", "pituicytoma", "PITUICYTOMA, BENIGN", "Pituicytoma (disorder)", "Pituicytoma (WHO Grade I)", "Pituicytoma (WHO Grade 1)", "pituicytoma (WHO grade I)", "posterior pituitary astrocytoma", "Posterior Pituitary Astrocytoma", "Pituicytoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pituicytoma", "shortest_name_length": 4}
{"curie": "MONDO:0017555", "names": ["radio-ulnar fusion, bilateral", "radio-ulnar synostosis, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radio-ulnar synostosis, bilateral", "shortest_name_length": 29}
{"curie": "UMLS:C5420442", "names": ["Refractory Esophageal Anastomotic Stricture"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Esophageal Anastomotic Stricture", "shortest_name_length": 43}
{"curie": "MONDO:0032802", "names": ["DFNA37", "DEAFNESS, AUTOSOMAL DOMINANT 37", "deafness, autosomal dominant 37", "hearing loss, autosomal dominant 37"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal dominant 37", "shortest_name_length": 6}
{"curie": "UMLS:C5237061", "names": ["Refractory Endometrial Mucinous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Endometrial Mucinous Adenocarcinoma", "shortest_name_length": 46}
{"curie": "UMLS:C0751043", "names": ["Monochromatopsia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Monochromatopsia", "shortest_name_length": 16}
{"curie": "UMLS:C4683428", "names": ["Stage I Thyroid Gland Follicular Cancer Under 55 Years", "Stage I Thyroid Gland Follicular Carcinoma Under 55 Years AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Thyroid Gland Follicular Carcinoma Under 55 Years AJCC v8", "shortest_name_length": 54}
{"curie": "UMLS:C0262977", "names": ["Achromia of skin", "Skin depigmented", "DECOLORATION SKIN", "Decoloration skin", "skin decoloration", "Decolouration skin", "SKIN DEPIGMENTATION", "Depigmentation skin", "Skin depigmentation", "DEPIGMENTATION SKIN", "skin depigmentation", "depigmentation of skin", "Depigmentation of skin", "Achromia of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Achromia of skin", "shortest_name_length": 16}
{"curie": "MONDO:0021677", "names": ["Postinfectious neuralgia", "postinfectious neuralgia", "post-infectious neuralgia", "Postinfectious neuralgia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "post-infectious neuralgia", "shortest_name_length": 24}
{"curie": "UMLS:C0020569", "names": ["Salivary gland hyperplasia", "Salivary Gland Hypertrophy", "Salivary gland enlargement", "ENLARGEMENT SALIVARY GLAND", "Enlargement salivary gland", "SALIVARY GLAND ENLARGEMENT", "salivary gland hypertrophy", "Salivary gland hypertrophy", "salivary glands hypertrophy", "salivary gland; hypertrophy", "hyperplasia; salivary gland", "hypertrophy; salivary gland", "Salivary gland enlargements", "salivary gland; hyperplasia", "Hypertrophy of salivary gland", "Salivary gland enlargement NOS", "hypertrophy of salivary glands", "Hypertrophy of salivary gland (disorder)", "hypertrophy of salivary glands (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypertrophy of salivary gland", "shortest_name_length": 26}
{"curie": "MONDO:0005673", "names": ["stasis syndrome", "Stasis syndrome", "Stasis Syndrome", "Blind Loop Syndrome", "blind loop syndrome", "Blind loop syndrome", "BLIND LOOP SYNDROME", "syndrome; blind loop", "Syndrome, Blind Loop", "blind loop; syndrome", "blind loop syndromes", "Stagnant Loop Syndrome", "stagnant loop syndrome", "Stagnant loop syndrome", "Loop Syndrome, Stagnant", "Stagnant Loop Syndromes", "Blind loop syndrome NOS", "Syndrome, Stagnant Loop", "Syndromes, Stagnant Loop", "Blind loop syndrome, NOS", "Loop Syndromes, Stagnant", "Stasis (Blind Loop) Syndrome", "stasis (blind loop) syndrome", "Bacterial overgrowth syndrome", "Bacterial Overgrowth Syndrome", "bacterial overgrowth syndrome", "Syndrome, Bacterial Overgrowth", "Blind loop syndrome (disorder)", "blind loop syndrome (diagnosis)", "Contaminated small bowel syndrome", "Bacterial overgrowth syndrome (disorder)", "bacterial overgrowth syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blind loop syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0020386", "names": ["DORV, Fallot type", "Fallot type double outlet right ventricle", "Double outlet right ventricle, Fallot type", "double outlet right ventricle, Fallot type", "Double Outlet Right Ventricle, Subaortic VSD", "double outlet from morphologic RV chamber with subaortic VSD", "DORV with subaortic or doubly committed VSD with pulmonary stenosis", "Double outlet right ventricle with subaortic ventricular septal defect", "Double outlet right ventricle with subaortic ventricular septal defect (disorder)", "double outlet from morphologic right ventricular chamber with subaortic ventricular septal defect", "double outlet from morphologic right ventricular chamber with subaortic ventricular septal defect (diagnosis)", "double outlet right ventricle with subaortic or doubly committed ventricular septal defect with pulmonary stenosis", "Double outlet right ventricle with subaortic or doubly committed ventricular septal defect with pulmonary stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "double outlet right ventricle with subaortic or doubly committed ventricular septal defect with pulmonary stenosis", "shortest_name_length": 17}
{"curie": "MONDO:0002341", "names": ["granulomatous angiitis", "Granulomatous angiitis", "Granulomatous Angiitis", "Angiitis, Granulomatous", "Granulomatous Arteritis", "Granulomatous arteritis", "granulomatous arteritis", "ARTERITIS, GRANULOMATOUS", "Granulomatous vasculitis", "granulomatous vasculitis", "Arteritis, Granulomatous", "Granulomatous vasculitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "granulomatous angiitis", "shortest_name_length": 22}
{"curie": "UMLS:C0855200", "names": ["Stage II Subdiaphragmatic Mixed Cellularity Hodgkin Lymphoma", "Stage II Subdiaphragmatic Mixed Cellularity Hodgkin's Disease", "Hodgkin's disease mixed cellularity stage II subdiaphragmatic", "Stage II Subdiaphragmatic Mixed Cellularity Hodgkin's Lymphoma", "Stage II Mixed Cellularity Hodgkin's Disease below the Diaphragm", "Stage II Mixed Cellularity Hodgkin's Lymphoma below the Diaphragm", "Stage II Subdiaphragmatic Mixed Cellularity Classical Hodgkin Lymphoma", "Ann Arbor Stage II Subdiaphragmatic Mixed Cellularity Classic Hodgkin Lymphoma", "Ann Arbor Stage II Subdiaphragmatic Mixed Cellularity Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's disease mixed cellularity stage II subdiaphragmatic", "shortest_name_length": 60}
{"curie": "MONDO:0035122", "names": ["GRIN2B-related developmental delay, intellectual disability and autism spectrum disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "GRIN2B-related developmental delay, intellectual disability and autism spectrum disorder", "shortest_name_length": 88}
{"curie": "UMLS:C0012241", "names": ["malformation gi", "GI malformation", "GI MALFORMATION", "Gastrointestinal anomaly", "GASTROINTESTINAL ANOMALY", "Gastrointestinal anomalies", "anomalies gastrointestinal", "Gastrointestinal malformation", "gastrointestinal malformation", "gastrointestinal malformations", "Gastrointestinal malformations", "anomaly; gastrointestinal tract", "gastrointestinal tract; anomaly", "Gastrointestinal malformation NOS", "Congenital digestive tract anomaly", "Gastrointestinal tract anomaly NOS", "Anomaly congenital gastrointestinal", "Congenital alimentary tract anomaly", "congenital anomaly of digestive tract", "Congenital anomaly of digestive tract", "Congenital anomaly of alimentary tract", "Congenital alimentary tract anomaly NOS", "Congenital alimentary tract anomaly, NOS", "Gastrointestinal tract malformation, NOS", "Gastrointestinal tract congenital anomaly", "ANOMALY CONGENITAL GASTROINTESTINAL (NOS)", "Congenital gastrointestinal malformations", "Congenital Alimentary Tract Malformations", "Alimentary tract malformation, congenital", "Congenital anomaly of gastrointestinal tract", "Congenital alimentary tract malformation NOS", "congenital anomaly of gastrointestinal tract", "Congenital anomaly of digestive tract (disorder)", "congenital anomaly of digestive tract (diagnosis)", "Congenital anomaly of gastrointestinal tract (disorder)", "congenital anomaly of gastrointestinal tract (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital anomaly of gastrointestinal tract", "shortest_name_length": 15}
{"curie": "MONDO:0009503", "names": ["PDHXD", "diaphorase deficiency", "Diaphorase deficiency", "2-oxoglutarate complex deficiency", "lipoamide dehydrogenase deficiency", "Lipoamide dehydrogenase deficiency", "lacticacidemia due to PDX1 deficiency", "Dihydrolipoyl dehydrogenase deficiency", "dihydrolipoyl dehydrogenase deficiency", "Glycine cleavage system L protein deficiency", "pyruvate dehydrogenase E3-binding protein deficiency", "Pyruvate dehydrogenase E3-binding protein deficiency", "Pyruvate Dehydrogenase E3-Binding Protein Deficiency", "pyruvate dehydrogenase E3-binding PROTEIN deficiency", "PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY", "Pyruvate dehydrogenase protein X component deficiency", "pyruvate dehydrogenase protein X component deficiency", "Pyruvate dehydrogenase complex component E3 deficiency", "pyruvate dehydrogenase complex component E3 deficiency", "branched chain alpha-ketoacid dehydrogenase complex deficiency", "Branched chain alpha-ketoacid dehydrogenase complex deficiency", "LACTIC ACIDEMIA DUE TO DEFECT IN LIPOYL-CONTAINING COMPONENT X OF THE PYRUVATE DEHYDROGENASE COMPLEX", "Lactic Acidemia due to Defect in Lipoyl-Containing Component X of the Pyruvate Dehydrogenase Complex", "lactic acidemia due to defect in lipoyl-containing component 10 of the pyruvate dehydrogenase Complex"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyruvate dehydrogenase E3-binding protein deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0010629", "names": ["Impacted teeth", "Multiple buried teeth", "Multiple retained teeth", "Multiple impacted teeth", "impacted teeth, multiple", "IMPACTED TEETH, MULTIPLE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "impacted teeth, multiple", "shortest_name_length": 14}
{"curie": "MONDO:0003125", "names": ["sex cord-stromal neoplasm", "testis sex cord-stromal tumor", "sex cord-stromal tumor of testis", "Sex Cord-Stromal tumor of testis", "Sex cord-stromal tumor of testis", "Sex cord stromal tumor of testis", "Sex Cord-Stromal Tumor of Testis", "Sex cord stromal tumour of testis", "testicular sex cord-stromal tumor", "Testicular Sex Cord-Stromal Tumor", "Testicular sex cord-stromal tumor", "sex cord-stromal neoplasm of testis", "Sex Cord-Stromal Neoplasm of Testis", "Testicular Sex Cord-Stromal Neoplasm", "testicular sex cord-stromal neoplasm", "Sex Cord-Stromal Tumor of the Testis", "sex cord-stromal tumor of the testis", "Sex Cord-Stromal Neoplasm of the Testis", "sex cord-stromal neoplasm of the testis", "Sex cord stromal tumor of testis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular sex cord-stromal neoplasm", "shortest_name_length": 25}
{"curie": "MONDO:0009773", "names": ["OODD", "ECTD16", "Fadhil syndrome", "ectodermal dysplasia", "Odontoonychodermal dysplasia", "odontoonychodermal dysplasia", "ODONTOONYCHODERMAL DYSPLASIA", "Odonto-onycho-dermal dysplasia", "odonto-onycho-dermal dysplasia", "Odonto-onycho-dermal dysplasia (disorder)", "ECTODERMAL DYSPLASIA 16, HYPO- OR HYPERHIDROTIC/HAIR/TOOTH/NAIL TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "odonto-onycho-dermal dysplasia", "shortest_name_length": 4}
{"curie": "MONDO:0010741", "names": ["STHAGX1", "EDA tooth agenesis", "hypodontia/oligodontia, X-linked, 1", "HYPODONTIA/OLIGODONTIA, X-LINKED, 1", "Hypodontia-Oligodontia, X-Linked, 1", "Tooth Agenesis, Selective, X-Linked, 1", "TOOTH AGENESIS, SELECTIVE, X-LINKED, 1", "tooth agenesis, selective, X-linked, 1", "tooth agenesis caused by mutation in EDA", "tooth agenesis, selective, X-linked, type 1", "tooth agenesis, selective, X-linked 1, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tooth agenesis, selective, X-linked, 1", "shortest_name_length": 7}
{"curie": "UMLS:C3665850", "names": ["Procedural intestinal perforation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Procedural intestinal perforation", "shortest_name_length": 33}
{"curie": "UMLS:C0344583", "names": ["Cor triloculare", "Cor Triloculare", "triloculare; cor", "cor; triloculare", "Cor triloculare (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cor triloculare", "shortest_name_length": 15}
{"curie": "MONDO:0005539", "names": ["small bowel Crohn disease", "small bowel Crohn's disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small bowel Crohn disease", "shortest_name_length": 25}
{"curie": "UMLS:C0853800", "names": ["Contrast media reaction", "contrast media reaction", "contrast media reactions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Contrast media reaction", "shortest_name_length": 23}
{"curie": "MONDO:0009177", "names": ["Epidermolysis bullosa, late-onset localized junctional, with mental retardation", "epidermolysis bullosa, late-onset localized junctional, with mental retardation", "EPIDERMOLYSIS BULLOSA, LATE-ONSET LOCALIZED JUNCTIONAL, WITH MENTAL RETARDATION", "epidermolysis bullosa, late-onset localized junctional, with intellectual disability", "late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome", "Epidermolysis bullosa simplex localisata associated with anodontia, hair and nail disorders", "epidermolysis bullosa simplex localisata associated with anodontia, hair and nail disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome", "shortest_name_length": 79}
{"curie": "UMLS:C4525126", "names": ["Stage IIIB Colon Cancer", "Stage IIIB Colon Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Colon Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "UMLS:C0030484", "names": ["Paraphrenia", "paraphrenia", "Paraphrenia, NOS", "Paraphrenia (disorder)", "paraphrenia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paraphrenia", "shortest_name_length": 11}
{"curie": "MONDO:0017429", "names": ["joint formation defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "joint formation defects", "shortest_name_length": 23}
{"curie": "MONDO:0014284", "names": ["SRTD10", "short-rib thoracic dysplasia 10 with or without polydactyly", "SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short-rib thoracic dysplasia 10 with or without polydactyly", "shortest_name_length": 6}
{"curie": "MONDO:0037736", "names": ["Infratentorial Tumor", "infratentorial tumor", "Tumor, Infratentorial", "Infratentorial Tumors", "Posterior Fossa Tumor", "infratentorial tumors", "Tumor, Posterior Fossa", "Posterior Fossa Tumors", "Infratentorial Neoplasm", "infratentorial neoplasm", "infratentorial neoplasms", "Posterior Fossa Neoplasm", "Neoplasm, Infratentorial", "Infratentorial Neoplasms", "Posterior Fossa Neoplasms", "Neoplasms, Infratentorial", "neoplasms, infratentorial", "Neoplasm, Posterior Fossa", "Neoplasms, Posterior Fossa", "brain neoplasms, infratentorial", "Brain Neoplasms, Infratentorial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infratentorial neoplasm", "shortest_name_length": 20}
{"curie": "MONDO:0007756", "names": ["HLP", "Flegel disease", "FLEGEL DISEASE", "Flegels disease", "Flegel's disease", "HYPERKERATOSIS LENTICULARIS PERSTANS", "Hyperkeratosis lenticularis perstans", "hyperkeratosis lenticularis perstans", "HLP - Hyperkeratosis lenticularis perstans", "hyperkeratosis lenticularis perstans (disease)", "hyperkeratosis lenticularis perstans of Flegel", "Hyperkeratosis lenticularis perstans of Flegel", "Hyperkeratosis lenticularis perstans (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperkeratosis lenticularis perstans", "shortest_name_length": 3}
{"curie": "MONDO:0008629", "names": ["uric acid urolithiasis", "urolithiasis, uric acid, autosomal dominant", "UROLITHIASIS, URIC ACID, AUTOSOMAL DOMINANT", "nephrolithiasis, uric acid, autosomal dominant", "NEPHROLITHIASIS, URIC ACID, AUTOSOMAL DOMINANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urolithiasis, uric acid, autosomal dominant", "shortest_name_length": 22}
{"curie": "MONDO:0006677", "names": ["Bile Reflux", "reflux bile", "bile reflux", "Bile reflux", "Reflux, Bile", "Bile reflux (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bile reflux", "shortest_name_length": 11}
{"curie": "UMLS:C5237352", "names": ["NMN", "Nail Matrix Nevus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nail Matrix Nevus", "shortest_name_length": 3}
{"curie": "UMLS:C1698097", "names": ["Intraoperative Digestive System Injury", "Intraoperative Gastrointestinal Injury", "Intraoperative gastrointestinal injury", "intraoperative gastrointestinal injury", "intraoperative gastrointestinal injury (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraoperative Digestive System Injury", "shortest_name_length": 38}
{"curie": "UMLS:C4684868", "names": ["Refractory Malignant Glioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Malignant Glioma", "shortest_name_length": 27}
{"curie": "UMLS:C0678052", "names": ["stage III adrenocortical cancer", "Stage III Adrenal Cortex Cancer", "Stage III Adrenal Cortex Carcinoma", "Stage III Adrenocortical Carcinoma", "Stage III Carcinoma of Adrenal Cortex", "Stage III Carcinoma of the Adrenal Cortex", "Stage III Adrenal Cortex Carcinoma AJCC v7", "Stage III Adrenal Cortical Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Adrenal Cortex Carcinoma AJCC v7", "shortest_name_length": 31}
{"curie": "UMLS:C0272398", "names": ["Dermatopathic lymphadenitis", "Lymphadenitis, dermatopathic", "Dermatopathic Lymphadenopathy", "Dermatopathic lymphadenopathy", "Lymphadenopathy, dermatopathic", "Dermatopathic lymphadenitis (disorder)", "Lipomelanotic reticuloendothelial cell hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dermatopathic lymphadenitis", "shortest_name_length": 27}
{"curie": "UMLS:C4551883", "names": ["Cervical Cancer Stage IVB", "Stage IVB Cervical Cancer", "AJCC Stage IVB Cervical Cancer", "FIGO Stage IVB Cervix Carcinoma", "Stage IVB Cervical Cancer AJCC v6", "Stage IVB Cervical Cancer AJCC v7", "FIGO Stage IVB Cervical Carcinoma", "FIGO Stage IVB Carcinoma of Cervix", "FIGO Stage IVB Cervix Uteri Carcinoma", "FIGO Stage IVB Carcinoma of the Cervix", "FIGO Stage IVB Uterine Cervix Carcinoma", "FIGO Stage IVB Carcinoma of Cervix Uteri", "Stage IVB Cervical Cancer AJCC v6 and v7", "FIGO Stage IVB Carcinoma of Uterine Cervix", "FIGO Stage IVB Carcinoma of the Cervix Uteri", "FIGO Stage IVB Carcinoma of the Uterine Cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Cervical Cancer AJCC v6 and v7", "shortest_name_length": 25}
{"curie": "UMLS:C0346378", "names": ["Medulloepithelioma of ciliary body", "Malignant Ciliary Body Medulloepithelioma", "Ciliary Body Malignant Medulloepithelioma", "malignant medulloepithelioma of ciliary body", "Malignant medulloepithelioma of ciliary body", "Malignant Medulloepithelioma of Ciliary Body", "Malignant Medulloepithelioma of the Ciliary Body", "Malignant medulloepithelioma of ciliary body (disorder)", "malignant medulloepithelioma of ciliary body (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant medulloepithelioma of ciliary body", "shortest_name_length": 34}
{"curie": "MONDO:0009328", "names": ["HEMANGIOMATOSIS, CUTANEOUS, WITH ASSOCIATED FEATURES", "hemangiomatosis, cutaneous, with associated features", "Hemangiomatosis, Cutaneous, with Associated Features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemangiomatosis, cutaneous, with associated features", "shortest_name_length": 52}
{"curie": "MONDO:0700084", "names": ["GMPPB-related myopathy", "myopathy caused by mutation in GMPPB", "myopathy caused by variation in GMPPB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy caused by variation in GMPPB", "shortest_name_length": 22}
{"curie": "MONDO:0018498", "names": ["DORV with subaortic or doubly committed VSD", "double outlet right ventricle with subaortic or doubly committed ventricular septal defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "double outlet right ventricle with subaortic or doubly committed ventricular septal defect", "shortest_name_length": 43}
{"curie": "UMLS:C4055246", "names": ["High-Risk Childhood Langerhans Cell Histiocytosis", "High Risk Childhood Langerhans Cell Histiocytosis", "Childhood Langerhans Cell Histiocytosis with Risk Organ Involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Langerhans Cell Histiocytosis with Risk Organ Involvement", "shortest_name_length": 49}
{"curie": "UMLS:C1691782", "names": ["Epstein-Barr viremia", "Epstein-Barr viraemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epstein-Barr viremia", "shortest_name_length": 20}
{"curie": "MONDO:0011137", "names": ["RP19", "RP 19", "RETINITIS PIGMENTOSA 19", "Retinitis Pigmentosa 19", "retinitis pigmentosa 19", "ABCA4 retinitis pigmentosa", "retinitis pigmentosa type 19", "retinitis pigmentosa caused by mutation in ABCA4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 19", "shortest_name_length": 4}
{"curie": "UMLS:C3899660", "names": ["Gemistocytic Astrocytoma", "childhood gemistocytic astrocytoma", "Childhood Gemistocytic Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Gemistocytic Astrocytoma", "shortest_name_length": 24}
{"curie": "UMLS:C2213266", "names": ["Thyroid Gland Follicular Dendritic Cell Sarcoma", "follicular dendritic cell sarcoma of thyroid gland", "follicular dendritic cell sarcoma of thyroid gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "follicular dendritic cell sarcoma of thyroid gland", "shortest_name_length": 47}
{"curie": "UMLS:C0473118", "names": ["Physiologic Hyperbilirubinemia", "Physiological Hyperbilirubinemia", "Physiological hyperbilirubinemia", "Physiological hyperbilirubinaemia", "Physiological hyperbilirubinemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Physiological hyperbilirubinemia (disorder)", "shortest_name_length": 30}
{"curie": "MONDO:0003540", "names": ["T-ALL", "Pro-T ALL", "Pre-T ALL", "Pre T-ALL", "Mature T ALL", "Mature T-ALL", "Cortical T ALL", "T-cell leukemia", "Acute T Cell Leukemia", "Acute T-Cell Leukemia", "acute T cell leukemia", "Leukemia, Acute T-Cell", "T Cell Leukemia, Acute", "Acute T-Cell Leukemias", "T-Cell Leukemia, Acute", "T-Cell Leukemias, Acute", "Leukemia, T-Cell, Acute", "Leukemias, Acute T-Cell", "T-cell type acute leukemia", "T-Cell Type Acute Leukemia", "T-cell type acute leukaemia", "Acute T-Lymphocytic Leukemia", "Leukemia, Acute T-Lymphocytic", "T-Lymphocytic Leukemia, Acute", "T Lymphocytic Leukemia, Acute", "Acute T-Lymphocytic Leukemias", "T Acute Lymphoblastic Leukemia", "Leukemias, Acute T-Lymphocytic", "T-Lymphocytic Leukemias, Acute", "T-Acute Lymphoblastic Leukemia", "T-Cell Acute Lymphocytic Leukemia", "T-cell acute lymphocytic leukaemia", "precursor T lymphoblastic leukemia", "Precursor T-Lymphoblastic Leukemia", "Precursor T Lymphoblastic Leukemia", "T-Cell Acute Lymphoblastic Leukemia", "Lymphocytic Leukemia, T Cell, Acute", "Acute T-cell lymphoblastic leukemia", "T-cell lymphoblastic leukemia acute", "T-cell acute lymphoblastic leukemia", "Lymphocytic Leukemia, T-Cell, Acute", "Acute T-Cell Lymphoblastic Leukemia", "Acute T Cell Lymphoblastic Leukemia", "Leukemia, Lymphocytic, Acute T Cell", "T-cell acute lymphoblastic leukaemia", "Leukemia, Lymphocytic, Acute, T-Cell", "Acute T-cell lymphoblastic leukaemia", "T-cell lymphoblastic leukaemia acute", "T-cell acute lymphoblastic leukemias", "Lymphoblastic Leukemia, Acute, T Cell", "Lymphoblastic Leukemia, Acute, T-Cell", "T-cell lymphoblastic leukemia/lymphoma", "Leukemia, Lymphoblastic, Acute, T-Cell", "Leukemia, Lymphoblastic, Acute, T Cell", "Precursor T Cell Lymphoblastic Lymphoma", "Precursor T-Cell Lymphoblastic Leukemia", "Precursor T-Cell Lymphoblastic Lymphoma", "Precursor T Cell Lymphoblastic Leukemia", "precursor T-cell lymphoblastic leukemia", "Precursor T-cell lymphoblastic leukemia", "Precursor T-cell lymphoblastic leukaemia", "Precursor T-cell acute lymphocytic leukemia", "precursor T-lymphoblastic lymphoma/leukemia", "Precursor T-cell acute lymphoblastic leukemia", "T-cell acute lymphoblastic leukemia (disorder)", "T-cell acute lymphoblastic leukemia (diagnosis)", "Precursor T Cell Lymphoblastic Leukemia Lymphoma", "Precursor T-Cell Lymphoblastic Leukemia-Lymphoma", "precursor T-cell lymphoblastic leukemia (diagnosis)", "Precursor T-cell acute lymphocytic leukemia/lymphoma", "Precursor T-cell acute lymphoblastic leukemia/lymphoma", "Precursor T-cell lymphoblastic leukemia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute T cell leukemia", "shortest_name_length": 5}
{"curie": "MONDO:0020286", "names": ["aortic malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic malformation", "shortest_name_length": 19}
{"curie": "UMLS:C5670707", "names": ["SMARCB1 Schwannomatosis 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SMARCB1 Schwannomatosis 1", "shortest_name_length": 25}
{"curie": "MONDO:0004369", "names": ["renal infection", "Renal infection", "infection renal", "kidney infection", "Kidney infection", "Infection;kidney", "infection kidney", "KIDNEY INFECTION", "infection kidneys", "kidney; infection", "Kidney Infections", "kidney infections", "infection; kidney", "infections kidney", "infections kidneys", "Infection of kidney", "of kidney infection", "infection of kidney", "Kidney infection NOS", "of kidney infections", "Infections of kidney", "Infection of kidney NOS", "renal infectious disease", "Infectious disorder of kidney", "infection of kidney (diagnosis)", "Infection of kidney, unspecified", "Infectious disorder of kidney (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal infectious disease", "shortest_name_length": 15}
{"curie": "MONDO:0013316", "names": ["OMD", "Omd", "OCMD", "Occult macular dystrophy", "occult macular dystrophy", "OCCULT MACULAR DYSTROPHY", "OMD - occult macular dystrophy", "OCMD - occult macular dystrophy", "corneal dystrophy macular occult", "Occult macular dystrophy (disorder)", "Occult macular dystrophy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "occult macular dystrophy", "shortest_name_length": 3}
{"curie": "OMIM:314700", "names": [], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"]}
{"curie": "MONDO:0032758", "names": ["NDCAMA", "NEURODEGENERATION, EARLY-ONSET, WITH CHOREOATHETOID MOVEMENTS AND MICROCYTIC ANEMIA", "neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia", "shortest_name_length": 6}
{"curie": "UMLS:C4054112", "names": ["Recurrent Undifferentiated High Grade Pleomorphic Sarcoma of Bone", "Recurrent Childhood Undifferentiated High Grade Pleomorphic Sarcoma", "Recurrent Childhood Undifferentiated High Grade Pleomorphic Sarcoma of Bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Undifferentiated High Grade Pleomorphic Sarcoma of Bone", "shortest_name_length": 65}
{"curie": "UMLS:C2986686", "names": ["stage IV AIDS-related lymphoma", "Stage IV AIDS-Related Lymphoma", "Ann Arbor Stage IV AIDS-Related Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage IV AIDS-Related Lymphoma", "shortest_name_length": 30}
{"curie": "UMLS:C4049313", "names": ["Vascular stent occlusion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vascular stent occlusion", "shortest_name_length": 24}
{"curie": "UMLS:C4682569", "names": ["Stage IB Uterine Corpus Endometrial Stromal Sarcoma", "Stage IB Uterine Corpus Endometrial Stromal Sarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Uterine Corpus Endometrial Stromal Sarcoma AJCC v8", "shortest_name_length": 51}
{"curie": "MONDO:0018030", "names": ["9p tetrasomy", "tetrasomy 9p", "Tetrasomy 9p", "Isochromosome 9p", "tetrasomy type 9p", "Mosaic tetrasomy 9p", "chromosome 9p tetrasomy", "Chromosome 9, tetrasomy 9p", "chromosome 9p tetrasomy syndrome", "Chromosome 9, tetrasomy 9p mosaicism", "Tetrasomy, short arm of chromosome 9", "Tetrasomy of short arm of chromosome 9", "tetrasomy of short arm of chromosome 9", "Tetrasomy of short arm of chromosome 9 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tetrasomy 9p", "shortest_name_length": 12}
{"curie": "MONDO:0002678", "names": ["Fibrosarcoma", "fibrosarcoma", "Pediatric Fibrosarcoma", "childhood fibrosarcoma", "pediatric fibrosarcoma", "Childhood Fibrosarcoma", "fibrosarcoma, childhood", "fibrosarcoma, pediatric", "sarcoma, fibro-, childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pediatric fibrosarcoma", "shortest_name_length": 12}
{"curie": "MONDO:0010861", "names": ["T1D3", "IDDM3", "TYPE 1 DIABETES MELLITUS 3", "type 1 diabetes mellitus 3", "INSULIN-DEPENDENT DIABETES MELLITUS 3", "insulin-dependent diabetes mellitus 3", "Insulin-Dependent Diabetes Mellitus 3", "DIABETES MELLITUS, INSULIN-DEPENDENT, 3", "diabetes mellitus, insulin-dependent, 3", "Diabetes Mellitus, Insulin-Dependent, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type 1 diabetes mellitus 3", "shortest_name_length": 4}
{"curie": "MONDO:0020368", "names": ["Axenfeld anomaly", "axenfeld anomaly", "Axenfeld Anomaly", "anomaly; Axenfeld", "axenfeld's anomaly", "Axenfeld's anomaly", "Anomaly, Axenfeld's", "Axenfeld; degeneration", "degeneration; Axenfeld", "Axenfeld-Rieger Anomaly", "Axenfeld-Rieger anomalies", "Axenfeld anomaly (disorder)", "Axenfeld; anomaly or syndrome", "Axenfeld's anomaly (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Axenfeld anomaly", "shortest_name_length": 16}
{"curie": "UMLS:C0079758", "names": ["NML", "Grade 2", "NM lymphoma", "FM lymphoma", "nodular MC lymphoma", "Nodular Mixed Lymphoma", "nodular mixed lymphoma", "lymphoma, nodular mixed", "Follicular Lymphoma Grade 2", "Follicular lymphoma grade 2", "grade 2 follicular lymphoma", "Grade 2 Follicular Lymphoma", "Follicular Lymphoma, Grade 2", "Follicular lymphoma grade II", "Follicular lymphoma, grade 2", "Grade II Follicular Lymphoma", "Lymphoma, Follicular, Grade 2", "follicular mixed cell lymphoma", "nodular; reticulolymphosarcoma", "reticulolymphosarcoma; nodular", "Follicular Mixed-Cell Lymphoma", "Follicular Mixed Cell Lymphoma", "Reticulolymphosarcoma, nodular", "Mixed-Cell Lymphoma, Follicular", "Follicular Mixed-Cell Lymphomas", "Mixed Cell Lymphoma, Follicular", "lymphoma, follicular mixed cell", "mixed cell lymphoma, follicular", "Lymphoma, Follicular Mixed-Cell", "Lymphomas, Follicular Mixed-Cell", "Lymphoma, Mixed-Cell, Follicular", "Mixed-Cell Lymphomas, Follicular", "Lymphoma, Follicular, Mixed Cell", "Reticulolymphosarcoma, follicular", "follicular; reticulolymphosarcoma", "reticulolymphosarcoma; follicular", "nodular; lymphoma, mixed (cell type)", "lymphoma; nodular, mixed (cell type)", "lymphoma; follicular, mixed cell type", "follicular; lymphoma, mixed cell type", "lymphoma; mixed cell type, follicular", "Lymphosarcoma, mixed cell type, nodular", "grade 2 follicular lymphoma (diagnosis)", "Grade II Follicular Mixed Cell Lymphoma", "grade II follicular mixed cell lymphoma", "lymphosarcoma; follicular, mixed cell type", "WHO Follicular Lymphoma Histologic Grade 2", "follicular; lymphosarcoma, mixed cell type", "Lymphosarcoma, mixed cell type, follicular", "Malignant lymphoma, mixed cell type, nodular", "Lymphoma, Nodular, Mixed Small and Large Cell", "Follicular malignant lymphoma, mixed cell type", "Malignant lymphoma, mixed cell type, follicular", "Follicular malignant lymphoma - mixed cell type", "nodular; lymphoma, mixed lymphocytic-histiocytic", "Lymphoma, Nodular, Mixed Lymphocytic Histiocytic", "lymphoma; nodular, mixed lymphocytic-histiocytic", "Lymphoma, Nodular, Mixed Lymphocytic-Histiocytic", "Follicular Mixed Lymphocytic-Histiocytic Lymphoma", "Lymphoma, Follicular, Small and Large Cleaved-Cell", "Lymphoma, Follicular, Small and Large Cleaved Cell", "Lymphoma, Follicular, Mixed Lymphocytic-Histiocytic", "Lymphoma, Follicular, Mixed Small and Large Lymphoid", "Follicular lymphoma, grade 2 (morphologic abnormality)", "malignant neoplasm nodular lymphoma follicular grade 2", "follicular; lymphoma, small cell, cleaved, and large cell", "lymphoma; follicular, small cell, cleaved, and large cell", "Malignant lymphoma, mixed lymphocytic-histiocytic, nodular", "Follicular malignant lymphoma - mixed cell type (disorder)", "Follicular malignant lymphoma, mixed cell type (diagnosis)", "Malignant lymphoma, mixed small cell and large cell, nodular", "[M]Malignant lymphoma, mixed lymphocytic-histiocytic, nodular", "Malignant lymphoma, mixed lymphocytic-histiocytic, follicular", "Malignant lymphoma, mixed small cell and large cell, follicular", "Malignant lymphoma, follicular, mixed small cleaved and large cell", "Follicular malignant lymphoma - mixed small cleaved and large cell", "Follicular non-Hodgkin mixed small cleaved and large cell lymphoma", "Malignant lymphoma, mixed small cleaved and large cell, follicular", "Follicular non-Hodgkin's mixed small cleaved and large cell lymphoma", "follicular non-Hodgkin's lymphoma, mixed small cleaved and large cell", "Malignant lymphoma, mixed lymphocytic-histiocytic, nodular (disorder)", "Mixed small cleaved and large cell, follicular non-Hodgkin's lymphoma", "Follicular non-Hodgkin lymphoma, mixed small cleaved cell and large cell", "Follicular non-Hodgkin's lymphoma, mixed small cleaved cell and large cell", "Follicular non-Hodgkin's mixed small cleaved and large cell lymphoma (disorder)", "follicular non-Hodgkin's lymphoma, mixed small cleaved and large cell (diagnosis)", "Follicular non-Hodgkin's lymphoma, mixed small cleaved cell and large cell (clinical)", "Follicular non-Hodgkin's lymphoma, mixed small cleaved cell and large cell (disorder)", "Follicular non-Hodgkin's lymphoma, mixed small cleaved cell and large cell (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoma, Mixed-Cell, Follicular", "shortest_name_length": 3}
{"curie": "UMLS:C5555955", "names": ["Dedifferentiated Gastrointestinal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dedifferentiated Gastrointestinal Stromal Tumor", "shortest_name_length": 47}
{"curie": "UMLS:C4761262", "names": ["Local anesthetic systemic toxicity", "Local anaesthetic systemic toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Local anesthetic systemic toxicity", "shortest_name_length": 34}
{"curie": "UMLS:C1328540", "names": ["Peripheral vasodilatation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peripheral vasodilatation", "shortest_name_length": 25}
{"curie": "UMLS:C1327920", "names": ["Childhood CML", "childhood CML", "childhood chronic myeloid leukemia", "Childhood Chronic Myeloid Leukemia", "Chronic Myelogenous Leukemia (CML)", "Childhood Chronic Myelogenous Leukemia", "childhood chronic myelogenous leukemia", "chronic myelogenous leukemia, childhood", "Childhood Chronic Myelogenous Leukemia, BCR-ABL1 Positive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Chronic Myelogenous Leukemia, BCR-ABL1 Positive", "shortest_name_length": 13}
{"curie": "UMLS:C1096309", "names": ["Myolipoma", "myolipoma", "Lipoleiomyoma", "Myolipoma (disorder)", "myolipoma (diagnosis)", "Myolipoma of Soft Tissue", "Extrauterine Lipoleiomyoma", "myolipoma; unspecified site", "Myolipoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myolipoma", "shortest_name_length": 9}
{"curie": "UMLS:C1334621", "names": ["Malignant Splenic Soft Tissue Tumor", "Malignant Soft Tissue Tumor of Spleen", "Malignant Splenic Soft Tissue Neoplasm", "Malignant Soft Tissue Neoplasm of Spleen", "Malignant Soft Tissue Tumor of the Spleen", "Malignant Soft Tissue Neoplasm of the Spleen"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Splenic Soft Tissue Neoplasm", "shortest_name_length": 35}
{"curie": "MONDO:0019642", "names": ["HVDRR", "VDDR2", "VDRR II", "VDDR II", "Vitamin D Dependent Rickets 2", "vitamin D receptor deficiency", "vitamin D dependent rickets 2", "Vitamin D Receptor Deficiency", "vitamin D-dependent rickets type II", "vitamin D-resistant rickets type II", "vitamin D-dependent rickets, type 2", "hereditary vitamin D-resistant rickets", "hypocalcemic vitamin D-resistant rickets", "hereditary 1,25 dihydroxyvitamin D-resistant rickets with abnormal Vitamin D receptor", "Hereditary 1,25 Dihydroxyvitamin D-resistant Rickets with Abnormal Vitamin D Receptor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitamin D-dependent rickets, type 2", "shortest_name_length": 5}
{"curie": "UMLS:C0234526", "names": ["Sensory apraxia", "Ideational apraxia", "Ideational Apraxia", "Ideational Apraxias", "Apraxia, Ideational", "Ideational dyspraxia", "Apraxias, Ideational", "Sensory apraxia (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ideational Apraxia", "shortest_name_length": 15}
{"curie": "MONDO:0013762", "names": ["PDHLD", "HGCLAS", "lipoic acid synthetase deficiency", "HYPERGLYCINEMIA, LACTIC ACIDOSIS, AND SEIZURES", "hyperglycinemia, lactic acidosis, and seizures", "PYRUVATE DEHYDROGENASE LIPOIC ACID SYNTHETASE DEFICIENCY", "pyruvate dehydrogenase lipoic acid synthetase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lipoic acid synthetase deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0011860", "names": ["LPRS2", "LEPROSY, SUSCEPTIBILITY TO, 2", "leprosy, susceptibility to, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leprosy, susceptibility to, 2", "shortest_name_length": 5}
{"curie": "UMLS:C3839652", "names": ["IEFVPTC", "Solid papillary carcinoma with invasion", "Invasive Encapsulated Follicular Variant Papillary Carcinoma", "Solid papillary carcinoma with invasion (morphologic abnormality)", "Invasive Encapsulated Follicular Variant Thyroid Gland Papillary Carcinoma", "Follicular Variant Thyroid Gland Papillary Carcinoma, Encapsulated Subtype with Invasion", "Invasive encapsulated follicular variant of papillary thyroid carcinoma (invasive EFVPTC)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Solid papillary carcinoma with invasion", "shortest_name_length": 7}
{"curie": "MONDO:0008287", "names": ["GCPS", "greig syndrome", "Greig Syndrome", "Greig syndrome", "greigs syndrome", "Greig's Syndrome", "Greig's syndrome", "frontodigital syndrome", "Hootnick-Holmes syndrome", "Cephalopolysyndactyly Syndrome", "cephalopolysyndactyly syndrome", "Greig cephalosyndactyly syndrome", "Greig Cephalosyndactyly Syndrome", "polysyndactyly-dyscrania syndrome", "GREIG CEPHALOPOLYSYNDACTYLY SYNDROME", "Greig Cephalopolysyndactyly Syndrome", "Greig cephalopolysyndactyly syndrome", "polysyndactyly-peculiar skull syndrome", "Polysyndactyly with peculiar skull shape", "polysyndactyly with peculiar skull Shape", "POLYSYNDACTYLY WITH PECULIAR SKULL SHAPE", "polysyndactyly with peculiars skull shape", "Greig cephalopolysyndactyly (GCPS) syndrome", "Greig Cephalopolysyndactyly (Gcps) Syndrome", "skull peculiar shape-polysyndactyly syndrome", "polysyndactyly-craniofacial anomalies syndrome", "craniofacial anomalies-polysyndactyly syndrome", "Greig cephalopolysyndactyly syndrome (disorder)", "polysyndactyly-craniofacial dysmorphism syndrome", "craniofacial dysmorphism-polysyndactyly syndrome", "familial polysyndactyly-craniofacial anomalies syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Greig cephalopolysyndactyly syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0221154", "names": ["Episodic hypertension", "paroxysmal hypertension", "Paroxysmal Hypertension", "Hypertension paroxysmal", "Paroxysmal hypertension", "Hypertension, paroxysmal", "HYPERTENSION, PAROXYSMAL", "Paroxysmal hypertension (disorder)", "paroxysmal hypertension was observed", "paroxysmal hypertension (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paroxysmal hypertension", "shortest_name_length": 21}
{"curie": "OMIM:615021", "names": [], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"]}
{"curie": "UMLS:C5237452", "names": ["Second Primary Squamous Cell Carcinoma of the Head and Neck"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Second Primary Squamous Cell Carcinoma of the Head and Neck", "shortest_name_length": 59}
{"curie": "MONDO:0010777", "names": ["infantile hypertrophic cardiomyopathy", "CARDIOMYOPATHY, INFANTILE HYPERTROPHIC", "cardiomyopathy, infantile hypertrophic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiomyopathy, infantile hypertrophic", "shortest_name_length": 37}
{"curie": "MONDO:0012417", "names": ["Heart-hand syndrome Slovenian type", "heart-hand syndrome, Slovenian type", "Heart-hand syndrome, Slovenian type", "HEART-HAND SYNDROME, SLOVENIAN TYPE", "Atriodigital dysplasia Slovenian type", "atriodigital dysplasia, Slovenian type", "Atriodigital dysplasia, Slovenian type", "Heart-hand syndrome Slovenian type (disorder)", "Cardiac conduction disease-dilated cardiomyopathy-brachydactyly syndrome", "Cardiac conduction disease with dilated cardiomyopathy and brachydactyly syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heart-hand syndrome, Slovenian type", "shortest_name_length": 34}
{"curie": "MONDO:0014325", "names": ["PC4", "pachyonychia congenita 4", "PACHYONYCHIA CONGENITA 4", "KRT6B pachyonychia congenita", "pachyonychia congenita type 4", "pachyonychia congenita caused by mutation in KRT6B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pachyonychia congenita 4", "shortest_name_length": 3}
{"curie": "MONDO:0013442", "names": ["JBTS11", "NPHP12", "nephronophthisis 12", "NEPHRONOPHTHISIS 12", "Joubert syndrome 11", "JOUBERT SYNDROME 11", "nephronophthisis type 12", "TTC21B nephronophthisis (disease)", "nephronophthisis (disease) caused by mutation in TTC21B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephronophthisis 12", "shortest_name_length": 6}
{"curie": "UMLS:C5190725", "names": ["Uterine fibroid with abnormal uterine bleeding", "Abnormal uterine bleeding due to uterine fibroid", "Abnormal uterine bleeding due to uterine fibroid (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abnormal uterine bleeding due to uterine fibroid", "shortest_name_length": 46}
{"curie": "UMLS:C0242670", "names": ["Vegetative state chronic", "Chronic vegetative state", "chronic vegetative state", "Persistent vegetative state", "persistent vegetative state", "Persistent Vegetative State", "persistent state vegetative", "Vegetative State, Persistent", "Persistent Vegetative States", "Persistent Unawareness State", "State, Persistent Vegetative", "Vegetative States, Persistent", "Persistent Unawareness States", "States, Persistent Vegetative", "State, Persistent Unawareness", "Unawareness State, Persistent", "Unawareness States, Persistent", "States, Persistent Unawareness", "PVS (Persistent Vegetative State)", "PVS - Persistent vegetative state", "PVSs (Persistent Vegetative State)", "Persistent vegetative state (disorder)", "persistent vegetative state (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Persistent Vegetative State", "shortest_name_length": 24}
{"curie": "UMLS:C1516707", "names": ["Colorectal Cancer by Astler-Coller Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Cancer by Astler-Coller Stage", "shortest_name_length": 40}
{"curie": "UMLS:C3178789", "names": ["Chronic Widespread Pain", "Widespread Chronic Pain", "Pain, Widespread Chronic", "Chronic Pain, Widespread", "Widespread Chronic Pains", "Pains, Widespread Chronic", "Chronic Pains, Widespread", "Pain Amplification Syndrome", "Amplified Musculoskeletal Pain Syndrome", "Amplified musculoskeletal pain syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Widespread Chronic Pain", "shortest_name_length": 23}
{"curie": "UMLS:C1335908", "names": ["Salivary Gland Sebaceous Adenoma", "sebaceous adenoma of salivary gland", "sebaceous adenoma of salivary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sebaceous adenoma of salivary gland", "shortest_name_length": 32}
{"curie": "MONDO:0016918", "names": ["partial deletion of chromosome 20q", "partial monosomy of chromosome 20q", "partial deletion of the long arm of chromosome 20", "partial monosomy of the long arm of chromosome 20", "partial deletion of the long arm of chromosome type 20"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of the long arm of chromosome 20", "shortest_name_length": 34}
{"curie": "MONDO:0008759", "names": ["OGDHD", "Oxoglutaricaciduria", "oxoglutaricaciduria", "Oxoglutaric Aciduria", "Alpha KGD deficiency", "Alpha-Kgd deficiency", "ALPHA-KGD DEFICIENCY", "Oxoglutaric aciduria", "OXOGLUTARIC ACIDURIA", "oxoglutarate dehydrogenase deficiency", "OXOGLUTARATE DEHYDROGENASE DEFICIENCY", "2-ketoglutarate dehydrogenase deficiency", "2-Ketoglutarate Dehydrogenase Deficiency", "2-KETOGLUTARATE DEHYDROGENASE DEFICIENCY", "alpha-ketoglutarate dehydrogenase deficiency", "Alpha-ketoglutarate dehydrogenase deficiency", "ALPHA-KETOGLUTARATE DEHYDROGENASE DEFICIENCY", "ALPHA-ketoglutarate dehydrogenase deficiency", "2 alpha ketoglutarate dehydrogenase deficiency", "Deficiency of alpha-ketoglutarate dehydrogenase", "Deficiency of alpha-ketoglutarate dehydrogenase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oxoglutaricaciduria", "shortest_name_length": 5}
{"curie": "MONDO:0002942", "names": ["Sebaceous Epithelioma", "Sebaceous epithelioma", "Basosebaceous Epithelioma", "sebaceous basal cell carcinoma", "skin basosebaceous basal cell carcinoma", "Basal cell carcinoma with sebaceous differentiation", "Basal Cell Carcinoma with Sebaceous Differentiation", "Basal Cell Epithelioma with Sebaceous Differentiation", "Skin Basal Cell Carcinoma with Sebaceous Differentiation", "skin nasal cell carcinoma with sebaceous differentiation", "Basal cell carcinoma with sebaceous differentiation (disorder)", "Basal cell carcinoma with sebaceous differentiation (diagnosis)", "malignant neoplasm carcinoma basal cell with sebaceous differentiation", "Basal cell carcinoma with sebaceous differentiation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sebaceous basal cell carcinoma", "shortest_name_length": 21}
{"curie": "UMLS:C4553876", "names": ["IVA", "Stage IVA Thyroid Gland Papillary Cancer", "Stage IVA Thyroid Gland Papillary Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Thyroid Gland Papillary Carcinoma AJCC v8", "shortest_name_length": 3}
{"curie": "UMLS:C1706923", "names": ["Benign Mixed Epithelial and Mesenchymal Hair Follicle Tumor", "Benign Mixed Epithelial and Mesenchymal Hair Follicle Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Mixed Epithelial and Mesenchymal Hair Follicle Neoplasm", "shortest_name_length": 59}
{"curie": "MONDO:0017980", "names": ["dobrow syndrome", "syngnathia multiple anomalies", "syngnathia-multiple anomalies syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syngnathia multiple anomalies", "shortest_name_length": 15}
{"curie": "MONDO:0023182", "names": ["Franceschini Vardeu Guala syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Franceschini Vardeu Guala syndrome", "shortest_name_length": 34}
{"curie": "UMLS:C0854391", "names": ["aorta injury", "Aortic Injury", "Aortic injury", "aorta; injury", "injury; aorta", "aortic injury", "Injury of aorta", "injury of aorta", "Injury of aorta NOS", "Injury of aorta (disorder)", "injury of aorta (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aortic Injury", "shortest_name_length": 12}
{"curie": "MONDO:0012226", "names": ["FEB5", "familial febrile seizures 5", "FEBRILE SEIZURES, FAMILIAL, 5", "febrile seizures, familial, 5", "Seizures, Familial Febrile, 5", "familial febrile convulsions 5", "FEBRILE CONVULSIONS, FAMILIAL, 5", "Convulsions, Familial Febrile, 5", "Febrile Convulsions, Familial, 5", "CONVULSIONS, FAMILIAL FEBRILE, 5", "convulsions, familial febrile, 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "febrile seizures, familial, 5", "shortest_name_length": 4}
{"curie": "MONDO:0800040", "names": ["MTND6 MELAS syndrome", "MELAS syndrome caused by mutation in MTND6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MELAS syndrome caused by mutation in MTND6", "shortest_name_length": 20}
{"curie": "UMLS:C5418888", "names": ["Advanced Ovarian Carcinosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Ovarian Carcinosarcoma", "shortest_name_length": 31}
{"curie": "MONDO:0016395", "names": ["O'Donnell Pappas syndrome", "O'Donnell-Pappas syndrome", "Foveal hypoplasia, presenile cataract", "foveal hypoplasia-presenile cataract syndrome", "Foveal hypoplasia-presenile cataract syndrome", "Foveal Hypoplasia and Presenile Cataract Syndrome", "Foveal hypoplasia with presenile cataract syndrome", "Foveal hypoplasia with presenile cataract syndrome (disorder)", "Foveal hypoplasia, congenital nystagmus, corneal pannus, and presenile cataracts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "foveal hypoplasia-presenile cataract syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0007939", "names": ["Mhs2", "MHS2", "malignant hyperthermia susceptibility 2", "Malignant hyperthermia susceptibility type 2", "malignant hyperthermia, susceptibility to, 2", "malignant hyperthermia susceptibility type 2", "MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 2", "Malignant hyperpyrexia susceptibility type 2", "malignant hyperpyrexia susceptibility type 2", "malignant hyperthermia, susceptibility to, type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant hyperthermia, susceptibility to, 2", "shortest_name_length": 4}
{"curie": "UMLS:C5419975", "names": ["Refractory Meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Meningioma", "shortest_name_length": 21}
{"curie": "MONDO:0013698", "names": ["DA1B", "distal type 1B arthrogryposis", "distal arthrogryposis type 1B", "arthrogryposis distal type 1b", "ARTHROGRYPOSIS, DISTAL, TYPE 1B", "arthrogryposis, distal, type 1B", "distal type 1B arthrogryposis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis, distal, type 1B", "shortest_name_length": 4}
{"curie": "MONDO:0019950", "names": ["MDC", "CMD", "congenital MD", "Congenital muscular dystrophy", "congenital muscular dystrophy", "Muscular dystrophy, congenital", "Congenital muscular dystrophy NOS", "Congenital hereditary muscular dystrophy", "MUSCULAR DYSTROPHY CONGENITAL HEREDITARY", "congenital hereditary muscular dystrophy", "Congenital muscular dystrophy (disorder)", "Congenital hereditary muscular dystrophy (disorder)", "congenital hereditary muscular dystrophy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital muscular dystrophy", "shortest_name_length": 3}
{"curie": "UMLS:C1736186", "names": ["Postoperative shivering"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postoperative shivering", "shortest_name_length": 23}
{"curie": "MONDO:0001290", "names": ["Trisymptome", "Allergic vasculitis", "allergic vasculitis", "Maladie trisymptome", "VASCULITIS ALLERGIC", "Vasculitis allergic", "vasculitis; allergic", "VASCULITIS, ALLERGIC", "allergic; vasculitis", "Vasculitis, allergic", "Gougerot-Ruiter syndrome", "HYPERSENSITIVITY ANGIITIS", "Leucocytoclastic angiitis", "leukocytoclastic angiitis", "Leukocytoclastic angiitis", "Hypersensitivity Angiitis", "Hypersensitivity angiitis", "hypersensitivity angiitis", "ANGIITIS, HYPERSENSITIVITY", "ANGIITIS, LEUKOCYTOCLASTIC", "Angiitis, Hypersensitivity", "hypersensitivity; angiitis", "angiitis; hypersensitivity", "Allergic Cutaneous Angiitis", "leukocytoclastic vasculitis", "leucocytoclastic vasculitis", "Hypersensitivity vasculitis", "vasculitis leukocytoclastic", "Leucocytoclastic vasculitis", "Leukocytoclastic vasculitis", "Hypersensitivity Angiitides", "allergic cutaneous angiitis", "Allergic cutaneous angiitis", "hypersensitivity vasculitis", "Hypersensitivity Vasculitis", "VASCULITIS, LEUKOCYTOCLASTIC", "Cutaneous Angiitis, Allergic", "Angiitides, Hypersensitivity", "Vasculitis, Hypersensitivity", "Angiitis, Allergic Cutaneous", "Cutaneous Allergic Vasculitis", "allergic cutaneous vasculitis", "Allergic cutaneous vasculitis", "Allergic Cutaneous Vasculitis", "Allergic Cutaneous Angiitides", "Hypersensitivity Vasculitides", "VASCULITIDES, HYPERSENSITIVITY", "Cutaneous Vasculitis, Allergic", "Cutaneous Angiitides, Allergic", "Allergic Vasculitis, Cutaneous", "Angiitides, Allergic Cutaneous", "Vasculitis, Cutaneous Allergic", "Vasculitides, Hypersensitivity", "Vasculitis, Allergic Cutaneous", "Cutaneous Allergic Vasculitides", "Allergic cutaneous arteriolitis", "Allergic Cutaneous Vasculitides", "Cutaneous Vasculitides, Allergic", "Vasculitides, Allergic Cutaneous", "Vasculitides, Cutaneous Allergic", "Dermatitis nodularis necroticans", "Allergic Vasculitides, Cutaneous", "Cutaneous small vessel vasculitis", "Benign leukocytoclastic vasculitis", "Hypersensitivity angiitis syndrome", "Cutaneous leucocytoclastic angiitis", "Cutaneous Leukocytoclastic Angiitis", "Cutaneous leukocytoclastic angiitis", "Autoimmune Hypersensitivity angiitis", "Hypersensitivity angiitis (disorder)", "autoimmune hypersensitivity angiitis", "Angiitis, Cutaneous Leukocytoclastic", "Leukocytoclastic Angiitis, Cutaneous", "Cutaneous Leukocytoclastic Vasculitis", "Cutaneous Leukocytoclastic Angiitides", "hypersensitivity angiitis (diagnosis)", "Cutaneous hypersensitivity vasculitis", "Leukocytoclastic Angiitides, Cutaneous", "Vasculitis, Cutaneous Leukocytoclastic", "Hypersensitivity angiitis, unspecified", "Angiitides, Cutaneous Leukocytoclastic", "Leukocytoclastic Vasculitis, Cutaneous", "hypersensitivity vasculitis (diagnosis)", "Vasculitis, Leukocytoclastic, Cutaneous", "Cutaneous Leukocytoclastic Vasculitides", "Vasculitides, Cutaneous Leukocytoclastic", "Leukocytoclastic Vasculitides, Cutaneous", "Cutaneous leukocytoclastic angiitis (disorder)", "VASCULITIS NONSPECIFIC ALLERGIC HYPERSENSITIVITY VASCULITIS", "VASCULITIS NONSPECIFIC ALLERGIC <HYPERSENSITIVITY VASCULITIS>"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "allergic cutaneous vasculitis", "shortest_name_length": 11}
{"curie": "MONDO:0008128", "names": ["ophthalmoplegia, familial static", "Ophthalmoplegia, Familial Static", "OPHTHALMOPLEGIA, FAMILIAL STATIC", "External Ophthalmoplegia, Congenital Hereditary Nonprogressive", "EXTERNAL OPHTHALMOPLEGIA, NONPROGRESSIVE, CONGENITAL HEREDITARY", "external ophthalmoplegia, nonprogressive, congenital hereditary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ophthalmoplegia, familial static", "shortest_name_length": 32}
{"curie": "UMLS:C1513470", "names": ["Monodermal Testicular Teratoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Monodermal Testicular Teratoma", "shortest_name_length": 30}
{"curie": "UMLS:C0559546", "names": ["AR", "ADR", "Adverse Effect", "adverse effect", "Adverse Reaction", "ADVERSE REACTION", "adverse reaction", "Adverse reaction", "reactions adverse", "adverse reactions", "Adverse reactions", "Adverse reaction (disorder)", "adverse reaction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adverse reactions", "shortest_name_length": 2}
{"curie": "MONDO:0007842", "names": ["EDS11", "EDS XI", "EDS Xi", "EDS11, formerly", "EDS11, FORMERLY", "EDS XI, FORMERLY", "EDS Xi, formerly", "EDS 11 (formerly)", "familial joint laxity", "Familial joint laxity", "JOINT LAXITY, FAMILIAL", "Joint laxity, familial", "joint laxity, familial", "Joint instability syndrome", "Ehlers-Danlos syndrome type XI", "Ehlers-Danlos syndrome, type 11", "Ehlers-Danlos syndrome, type Xi", "Articular hypermobility syndrome", "articular hypermobility syndrome", "ARTICULAR HYPERMOBILITY SYNDROME", "familial joint instability syndrome", "FAMILIAL JOINT INSTABILITY SYNDROME", "Familial joint instability syndrome", "Ehlers-Danlos syndrome type 11, formerly", "EHLERS-DANLOS SYNDROME, TYPE XI, FORMERLY", "Familial articular hypermobility syndrome", "Ehlers-Danlos syndrome, type Xi, formerly", "Ehlers-Danlos syndrome, type 11 (formerly)", "Familial generalized articular hypermobility", "Familial generalised articular hypermobility", "Ehlers-Danlos syndrome familial joint laxity type", "Ehlers-Danlos syndrome, familial joint laxity type", "Ehlers-Danlos syndrome, familial joint laxity type (disorder)", "Ehlers-Danlos syndrome, familial joint laxity type (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "joint laxity, familial", "shortest_name_length": 5}
{"curie": "UMLS:C0349577", "names": ["Benign neoplasm of pinna", "Benign External Ear Tumor", "Benign neoplasm of auricle", "Benign Tumor of External Ear", "Benign tumor of external ear", "Benign External Ear Neoplasm", "Benign tumour of external ear", "Benign Neoplasm of External Ear", "Benign Tumor of the External Ear", "Benign neoplasm of auricle of ear", "Benign Neoplasm of the External Ear", "Benign External Auditory Canal Neoplasm", "Benign tumor of external ear (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign tumor of external ear", "shortest_name_length": 24}
{"curie": "MONDO:0005067", "names": ["Monophasic Synovial Sarcoma", "monophasic synovial sarcoma", "Monophasic Sarcoma of Synovium", "monophasic sarcoma of synovium", "Monophasic sarcoma of Synovium", "Monophasic Sarcoma of the Synovium", "monophasic sarcoma of the synovium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "monophasic synovial sarcoma", "shortest_name_length": 27}
{"curie": "MONDO:0016353", "names": ["Powell-Venencie-Gordon syndrome", "Powell Venencie Gordon syndrome", "Keratoderma and spastic paralysis", "keratoderma palmoplantar spastic paralysis", "Punctate keratoderma and spastic paralysis", "Palmoplantar keratoderma-spastic paralysis syndrome", "palmoplantar keratoderma-spastic paralysis syndrome", "Palmoplantar keratoderma, spastic paralysis syndrome", "palmoplantar hyperkeratosis-spastic paralysis syndrome", "Palmoplantar hyperkeratosis-spastic paralysis syndrome", "Palmoplantar keratoderma, spastic paralysis syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "palmoplantar keratoderma-spastic paralysis syndrome", "shortest_name_length": 31}
{"curie": "MONDO:0012828", "names": ["ATFB7", "atrial fibrillation familial 7", "atrial fibrillation, familial, 7", "Atrial Fibrillation, Familial, 7", "ATRIAL FIBRILLATION, FAMILIAL, 7", "KCNA5 familial atrial fibrillation", "atrial fibrillation, familial, type 7", "atrial fibrillation familial 7 (diagnosis)", "familial atrial fibrillation caused by mutation in KCNA5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial fibrillation, familial, 7", "shortest_name_length": 5}
{"curie": "UMLS:C0919988", "names": ["Metastatic bronchial carcinoma", "Metastatic bronchiogenic carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic bronchial carcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0003336", "names": ["ANE", "acute necrotizing encephalitis", "Acute necrotising encephalitis", "Acute Necrotizing Encephalitis", "Acute necrotizing encephalitis", "Necrotizing Encephalitis, Acute", "Encephalitis, Acute Necrotizing", "acute necrotizing encephalopathy", "Acute Necrotizing Encephalitides", "Necrotizing Encephalitides, Acute", "Encephalitides, Acute Necrotizing", "Acute necrotising viral encephalitis", "viral encephalitis acute necrotizing", "Acute necrotizing viral encephalitis", "Acute necrotizing encephalitis (disorder)", "Acute necrotizing encephalitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute necrotizing encephalitis", "shortest_name_length": 3}
{"curie": "UMLS:C5206895", "names": ["Localized Malignant Brain Neoplasm", "Non-Metastatic Malignant Brain Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized Malignant Brain Neoplasm", "shortest_name_length": 34}
{"curie": "UMLS:C4524712", "names": ["Clinical Stage I Gastroesophageal Junction Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage I Gastroesophageal Junction Adenocarcinoma AJCC v8", "shortest_name_length": 65}
{"curie": "MONDO:0020163", "names": ["canthal anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canthal anomaly", "shortest_name_length": 15}
{"curie": "MONDO:0002340", "names": ["tactile epilepsy", "Tactile Epilepsy", "Tactile epilepsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tactile epilepsy", "shortest_name_length": 16}
{"curie": "MONDO:0021826", "names": ["aerobic Actinomyces infection", "Aerobic actinomyces infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aerobic Actinomyces infection", "shortest_name_length": 29}
{"curie": "UMLS:C5669838", "names": ["Extramedullary Disease in Multiple Myeloma Involving the Lung", "Extramedullary Disease in Plasma Cell Myeloma Involving the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extramedullary Disease in Plasma Cell Myeloma Involving the Lung", "shortest_name_length": 61}
{"curie": "MONDO:0019164", "names": ["6q terminal deletion syndrome", "6q terminal deletion syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "6q terminal deletion syndrome", "shortest_name_length": 29}
{"curie": "UMLS:C0746351", "names": ["LYMPHOPROLIFERATIVE DISORDER BENIGN", "Benign Lymphoproliferative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Lymphoproliferative Disorder", "shortest_name_length": 35}
{"curie": "MONDO:0016170", "names": ["chronic polyradiculoneuropathy", "polyradiculoneuropathy, chronic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic polyradiculoneuropathy", "shortest_name_length": 30}
{"curie": "UMLS:C0393787", "names": ["Secondary trigeminal neuralgia", "Secondary Trigeminal Neuralgia", "trigeminal neuralgia secondary", "Secondary Trigeminal Neuralgias", "Neuralgia, Secondary Trigeminal", "Trigeminal Neuralgia, Secondary", "Secondary trigeminal neuralgia (disorder)", "Secondary trigeminal neuralgia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary Trigeminal Neuralgia", "shortest_name_length": 30}
{"curie": "UMLS:C5557369", "names": ["Vulvar Prepubertal Fibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Prepubertal Fibroma", "shortest_name_length": 26}
{"curie": "MONDO:0001000", "names": ["Mixed dust fibrosis", "mineral duct pneumoconiosis", "mineral dust pneumoconiosis", "pneumoconiosis from mineral dust", "mixed mineral dust pneumoconiosis", "Mixed mineral dust pneumoconiosis", "Mixed Mineral Dust Pneumoconiosis", "Mixed mineral dust pneumoconiosis (disorder)", "Mixed mineral dust pneumoconiosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed mineral dust pneumoconiosis", "shortest_name_length": 19}
{"curie": "MONDO:0000664", "names": ["apperceptive agnosia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "apperceptive agnosia", "shortest_name_length": 20}
{"curie": "MONDO:0024456", "names": ["IGDA", "ASGD3", "IRID1", "IGDA syndrome", "Iridogoniodysgenesis type1", "FOXC1 iridogoniodysgenesis", "iridogoniodysgenesis type 1", "Iridogoniodysgenesis, Type 1", "IRIDOGONIODYSGENESIS, TYPE 1", "iridogoniodysgenesis, type 1", "iris hypoplasia with glaucoma", "glaucoma iridogoniodysgenesia", "anterior segment dysgenesis 3", "glaucoma iridogoniodysplasia, familial", "GLAUCOMA IRIDOGONIODYSPLASIA, FAMILIAL", "Glaucoma Iridogoniodysplasia, Familial", "Iridogoniodysgenesis anomaly, Autosomal dominant", "IRIDOGONIODYSGENESIS ANOMALY, AUTOSOMAL DOMINANT", "iridogoniodysgenesis caused by mutation in FOXC1", "anterior segment dysgenesis 3, multiple subtypes", "iridogoniodysgenesis anomaly, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anterior segment dysgenesis 3", "shortest_name_length": 4}
{"curie": "UMLS:C2861609", "names": ["Acute Myeloid Leukemia with Multilineage Dysplasia in Remission", "Acute myeloid leukemia with multilineage dysplasia, in remission"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Myeloid Leukemia with Multilineage Dysplasia in Remission", "shortest_name_length": 63}
{"curie": "UMLS:C0262494", "names": ["GANGRENOUS CHOLECYSTITIS", "Gangrenous cholecystitis", "gangrenous cholecystitis", "cholecystitis; gangrenous", "gangrenous; cholecystitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gangrenous cholecystitis", "shortest_name_length": 24}
{"curie": "MONDO:0024528", "names": ["PEOA1", "autosomal dominant progressive external ophthalmoplegia 1", "PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL DOMINANT 1", "progressive external ophthalmoplegia, autosomal dominant 1", "Progressive External Ophthalmoplegia, Autosomal Dominant, 1", "POLG autosomal dominant progressive external ophthalmoplegia", "autosomal dominant progressive external ophthalmoplegia caused by mutation in POLG", "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1", "PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1", "Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1", "shortest_name_length": 5}
{"curie": "UMLS:C0750919", "names": ["Post-Ictal Aphasia", "Aphasia, Post-Ictal", "Aphasia, Post Ictal", "Post-Ictal Aphasias"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aphasia, Post-Ictal", "shortest_name_length": 18}
{"curie": "MONDO:0012103", "names": ["SCA25", "SPINOCEREBELLAR ATAXIA 25", "spinocerebellar ataxia 25", "Spinocerebellar ataxia 25", "spinocerebellar ataxia type 25", "Spinocerebellar ataxia type 25", "SCA25 Spinocerebellar ataxia 25", "Spinocerebellar ataxia type 25 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia type 25", "shortest_name_length": 5}
{"curie": "MONDO:0012985", "names": ["HS5", "SPH5", "SPHEROCYTOSIS, TYPE 5", "spherocytosis, type 5", "Spherocytosis, Type 5", "hereditary spherocytosis 5", "Spherocytosis, Hereditary, 5", "spherocytosis, hereditary, 5", "SPHEROCYTOSIS, HEREDITARY, 5", "EPB42 hereditary spherocytosis", "hereditary spherocytosis type 5", "hereditary spherocytosis caused by mutation in EPB42"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spherocytosis type 5", "shortest_name_length": 3}
{"curie": "MONDO:0018749", "names": ["HPFH-beta-thalassemia syndrome", "hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome", "shortest_name_length": 30}
{"curie": "MONDO:0016282", "names": ["CERMS", "Cervical rhabdomyosarcoma", "Cervical Rhabdomyosarcoma", "cervical rhabdomyosarcoma", "uterine cervix rhabdomyosarcoma", "Rhabdomyosarcoma of cervix uteri", "rhabdomyosarcoma of the cervix uteri", "Rhabdomyosarcoma of the cervix uteri", "uterine cervix rhabdomyosarcoma (disease)", "Rhabdomyosarcoma of cervix uteri (disorder)", "rhabdomyosarcoma (disease) of uterine cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rhabdomyosarcoma of the cervix uteri", "shortest_name_length": 5}
{"curie": "MONDO:0017823", "names": ["Somatoprolactinoma", "somatomammotropinoma", "Somatolactotropinoma", "GH and PRL cosecreting pituitary adenoma", "Growth hormone and prolactin cosecreting pituitary adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "somatomammotropinoma", "shortest_name_length": 18}
{"curie": "MONDO:0030523", "names": ["OOMD12", "oocyte maturation defect 12", "OOCYTE MATURATION DEFECT 12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oocyte maturation defect 12", "shortest_name_length": 6}
{"curie": "MONDO:0011218", "names": ["IHS", "IFAH", "ARIH", "ARCI11", "IFAH syndrome", "ichthyosis-hypotrichosis syndrome", "hypotrichosis-congenital ichthyosis syndrome", "autosomal recessive congenital ichthyosis 11", "ichthyosis, congenital, autosomal recessive 11", "ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 11", "Autosomal recessive ichthyosis with hypotrichosis", "autosomal recessive ichthyosis with hypotrichosis", "autosomal recessive congenital ichthyosis type 11", "ichthyosis with hypotrichosis, autosomal recessive", "ICHTHYOSIS WITH HYPOTRICHOSIS, AUTOSOMAL RECESSIVE", "Ichthyosis with hypotrichosis, autosomal recessive", "ichthyosis, congenital, autosomal recessive type 11", "ichthyosis-follicular atrophoderma-hypotrichosis syndrome", "Ichthyosis, Follicular Atrophoderma, Hypotrichosis, and Hypohidrosis", "ichthyosis-follicular atrophoderma-hypotrichosis-hypohidrosis syndrome", "ICHTHYOSIS AND FOLLICULAR ATROPHODERMA WITH HYPOTRICHOSIS AND HYPOHIDROSIS", "ichthyosis and follicular atrophoderma with hypotrichosis and hypohidrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive congenital ichthyosis 11", "shortest_name_length": 3}
{"curie": "MONDO:0006533", "names": ["cholesteatoma", "Epidermosis of ear", "Aural Cholesteatoma", "Aural Cholesteatomas", "Cholesteatoma, Aural", "Cholesteatomas, Aural", "EAR MIDDLE CHOLESTEATOMA", "Middle Ear Cholesteatoma", "cholesteatoma middle ear", "middle ear cholesteatoma", "Middle Ear Cholesteatomas", "Cholesteatoma, Middle Ear", "Epidermosis of middle ear", "epidermosis of middle ear", "Cholesteatomas, Middle Ear", "cholesteatoma of middle ear", "Cholesterosis of middle ear", "Cholesteatoma of Middle Ear", "Cholesteatoma of middle ear", "Cholesteatoma of the Middle Ear", "Cholesteatoma of the middle ear", "cholesteatoma of the middle ear", "middle ear cholesteatoma (disease)", "cholesteatoma (disease) of middle ear", "epidermosis of middle ear (diagnosis)", "Cholesteatoma of middle ear (disorder)", "cholesteatoma of middle ear and mastoid", "Cholesteatoma of middle ear and mastoid", "cholesteatoma of middle ear (diagnosis)", "cholesteatoma of middle ear and/or mastoid", "Cholesteatoma of middle ear and/or mastoid", "Cholesteatoma of middle ear and mastoid (disorder)", "unspecified cholesteatoma (morphologic abnormality)", "cholesteatoma of middle ear and mastoid (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholesteatoma of middle ear", "shortest_name_length": 13}
{"curie": "MONDO:0011478", "names": ["Roca syndrome", "ROCA SYNDROME", "ROCA Syndrome", "Roca-Weidemann syndrome", "ROCA-WEIDEMANN SYNDROME", "ROCA-Weidemann Syndrome", "growth and developmental retardation, ocular ptosis, cardiac defect, and anal atresia", "Growth and Developmental Retardation, Ocular Ptosis, Cardiac Defect, and Anal Atresia", "GROWTH AND DEVELOPMENTAL RETARDATION, OCULAR PTOSIS, CARDIAC DEFECT, AND ANAL ATRESIA", "growth and developintellectual disability, ocular ptosis, cardiac defect, and anal atresia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "growth and developintellectual disability, ocular ptosis, cardiac defect, and anal atresia", "shortest_name_length": 13}
{"curie": "UMLS:C4055371", "names": ["Borderline Ovarian Serous Tumor-Micropapillary Variant/Non-Invasive Low Grade Ovarian Serous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Ovarian Serous Tumor-Micropapillary Variant/Non-Invasive Low Grade Ovarian Serous Carcinoma", "shortest_name_length": 102}
{"curie": "UMLS:C0162810", "names": ["Hypertrophic scar", "scar; hypertrophy", "hypertrophy; scar", "Hypertrophic Scar", "hypertrophic scar", "scar; hypertrophic", "Hypertrophic scars", "Hypertrophic Scars", "hypertrophic; scar", "hypertrophic scars", "Scar, Hypertrophic", "Scars, Hypertrophic", "Hypertrophic Cicatrix", "Hypertrophic scarring", "hypertrophic scarring", "Hypertrophic cicatrix", "Cicatrix, Hypertrophic", "hypertrophic; cicatrix", "Hypertrophic Cicatrices", "Cicatrices, Hypertrophic", "Hypertrophic scar of skin", "Hypertrophic scar (disorder)", "hypertrophic scar (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cicatrix, Hypertrophic", "shortest_name_length": 17}
{"curie": "MONDO:0001808", "names": ["uterus involution", "involution uterus", "shrinking of uterus", "Involution of uterus", "involution of uterus", "Chronic subinvolution of uterus", "chronic subinvolution of uterus", "Chronic subinvolution of uterus (disorder)", "chronic subinvolution of uterus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic subinvolution of uterus", "shortest_name_length": 17}
{"curie": "MONDO:0014226", "names": ["ICL", "IMD13", "immunodeficiency 13", "IMMUNODEFICIENCY 13", "immunodeficiency type 13", "idiopathic Cd4 lymphopenia", "idiopathic CD4 lymphopenia", "IDIOPATHIC CD4 LYMPHOPENIA", "idiopathic CD4 lymphocytopenia", "Idiopathic CD4 lymphocytopenia", "ICL - idiopathic CD4 lymphocytopenia", "idiopathic CD4 positive T-lymphocytopenia", "Idiopathic CD4 lymphocytopenia (disorder)", "Idiopathic CD4 lymphocytopenia (diagnosis)", "lymphocyte disorder CD4 t deficiency idiopathic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic CD4 lymphocytopenia", "shortest_name_length": 3}
{"curie": "UMLS:C1332520", "names": ["Benign Non-Epithelial Gallbladder Neoplasm", "Gallbladder Benign Non-Epithelial Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gallbladder Benign Non-Epithelial Neoplasm", "shortest_name_length": 42}
{"curie": "MONDO:0021160", "names": ["bladder; gonorrhea", "gonorrhea; bladder", "cystitis gonococcal", "gonococcal cystitis", "Cystitis gonococcal", "Gonococcal cystitis", "gonococcal; cystitis", "Gonorrhea of bladder", "cystitis; gonococcal", "Cystitis in gonorrhea", "Cystitis in gonorrhoea", "Gonococcal cystitis (disorder)", "Neisseria gonorrhoeae cystitis", "Gonococcal cystitis (diagnosis)", "Neisseria gonorrhoeae caused cystitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gonococcal cystitis", "shortest_name_length": 18}
{"curie": "UMLS:C0855184", "names": ["Stage III Testicular Choriocarcinoma", "Testicular choriocarcinoma stage III", "Stage III Testicular Choriocarcinoma AJCC v6", "Stage III Testicular Choriocarcinoma AJCC v7", "Stage III Testicular Choriocarcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular choriocarcinoma stage III", "shortest_name_length": 36}
{"curie": "UMLS:C4525144", "names": ["stage IVC rectal cancer", "Stage IVC Rectal Cancer", "Stage IVC Rectal Cancer AJCC v8", "stage IVC rectal cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Rectal Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "UMLS:C0026919", "names": ["Mycobacterium; atypical", "atypical; Mycobacterium", "ATYPICAL MYCOBACTERIAL DISEASE", "atypical mycobacterial disease", "Atypical mycobacterial disease", "atypical mycobacterial infection", "Atypical mycobacterial infection", "Atypical Mycobacterium Infection", "MYCOBACTERIUM ATYPICAL INFECTION", "mycobacterium infection atypical", "atypical infections mycobacterial", "Mycobacterium Infection, Atypical", "Mycobacterial infection, atypical", "Atypical Mycobacterium Infections", "Atypical mycobacterial infections", "Mycobacterium Infections, Atypical", "Infections, Atypical Mycobacterium", "Atypical mycobacterium infection NOS", "Atypical mycobacterial infection NOS", "Atypical mycobacterial infection, NOS", "Infection due to mycobacterium, non-TB", "Nontuberculous Mycobacterium Infection", "Mycobacterium Infection, Nontuberculous", "Nontuberculous Mycobacterium Infections", "Mycobacterium Infections, Nontuberculous", "Atypical mycobacterial infection (disorder)", "atypical mycobacterial infection (diagnosis)", "Mycobacterial infection (excluding tuberculosis AND leprosy)", "Mycobacterial infection, NOS (excluding tuberculosis and leprosy)", "Mycobacterial infection (excluding tuberculosis AND leprosy) (disorder)", "Mycobacterial infectious disease, NOS (excluding tuberculosis and leprosy)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mycobacterium Infections, Nontuberculous", "shortest_name_length": 23}
{"curie": "UMLS:C3805175", "names": ["Appendicolith"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Appendicolith", "shortest_name_length": 13}
{"curie": "MONDO:0025488", "names": ["FELV", "Feline leukemia", "leukemia feline", "Feline Leukemia", "feline leukemia", "Leukemia, Feline", "Feline leukemias", "leukemia, feline", "Feline Leukemias", "leukemias, Feline", "Leukemias, Feline", "Feline leukemia virus infection", "Feline leukaemia virus infection", "Feline lymphosarcoma and leukemia", "Feline lymphosarcoma and leukaemia", "Feline lymphosarcoma AND/OR leukemia", "Feline visceral lymphoma and leukemia", "Feline lymphosarcoma AND/OR leukaemia", "Feline visceral lymphoma and leukaemia", "Feline visceral lymphoma AND/OR leukemia", "Feline visceral lymphoma AND/OR leukaemia", "Feline leukemia virus infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukemia, feline", "shortest_name_length": 4}
{"curie": "MONDO:0016801", "names": ["mitochondrial substrate carrier disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial substrate carrier disorder", "shortest_name_length": 40}
{"curie": "UMLS:C0235446", "names": ["AZOTEMIA RENAL", "Azotemia renal", "Renal azotemia", "renal azotemia", "Renal azotaemia", "Azotaemia renal", "Intrarenal azotemia", "Intrarenal azotaemia", "AZOTEMIA OF RENAL ORIGIN", "Azotemia of renal origin", "Azotaemia of renal origin", "Azotemia due to intrarenal disease", "Azotaemia due to intrarenal disease", "Azotemia due to intrarenal disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Azotemia due to intrarenal disease", "shortest_name_length": 14}
{"curie": "UMLS:C1333512", "names": ["Extrahepatic Bile Duct Tubular Adenoma", "Tubular Adenoma of Extrahepatic Bile Duct", "tubular adenoma of extrahepatic bile duct", "Tubular Adenoma of the Extrahepatic Bile Duct", "tubular adenoma of extrahepatic bile duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tubular adenoma of extrahepatic bile duct", "shortest_name_length": 38}
{"curie": "MONDO:0018978", "names": ["mediastinum fibrosis", "Fibrosis mediastinal", "mediastinal fibrosis", "MEDIASTINAL FIBROSIS", "FIBROSIS MEDIASTINAL", "Mediastinal Fibrosis", "Mediastinal fibrosis", "fibrosis; mediastinum", "Fibrous mediastinitis", "mediastinum; fibrosis", "fibrosing mediastinitis", "Fibrosing mediastinitis", "Fibrosis of mediastinum", "mediastinitis sclerosing", "sclerosing mediastinitis", "Sclerosing mediastinitis", "MEDIASTINITIS, SCLEROSING", "IgG4-related mediastinitis", "idiopathic mediastinal fibrosis", "Fibrosis of mediastinum (disorder)", "Sclerosing mediastinitis (disorder)", "fibrosing mediastinitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IgG4-related mediastinitis", "shortest_name_length": 20}
{"curie": "UMLS:C3640022", "names": ["Unilateral Anophthalmos", "Anophthalmos, Unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unilateral Anophthalmos", "shortest_name_length": 23}
{"curie": "MONDO:0024619", "names": ["CNS Infection", "cns infection", "CNS INFECTION", "CNS Infections", "cns infections", "Infection, CNS", "Infections, CNS", "Unusual CNS infection", "Central Nervous System Infection", "central infection nervous system", "central nervous system infection", "Central nervous system infection", "central infections nervous system", "Central Nervous System Infections", "central nervous system infections", "Central nervous system--Infections", "infections, central nervous system", "Infections, Central Nervous System", "Central nervous system infection NOS", "central nervous system infectious disease", "Central Nervous System Infectious Disease", "Central Nervous System Infectious Disorder", "central nervous system infectious disorder", "Infectious disease of central nervous system", "Infectious Disease of Central Nervous System", "infectious disease of central nervous system", "central nervous system infections (diagnosis)", "Infectious disease of central nervous system (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system infectious disorder", "shortest_name_length": 13}
{"curie": "MONDO:0010824", "names": ["Verloes syndrome", "VERLOES SYNDROME", "Verloes Gillerot Fryns syndrome", "Verloes-Gillerot-Fryns syndrome", "disorder of sex development intellectual disability", "pseudohermaphroditism-intellectual disability syndrome", "Cerebro-Acro-Visceral Early lethality multiplex syndrome", "Pseudohermaphroditism with intellectual disability syndrome", "Disorder of sex development-intellectual disability syndrome", "disorder of sex development-intellectual disability syndrome", "Disorder of sex development with intellectual disability syndrome", "disorder of sex development with intellectual disability syndrome", "Male pseudohermaphroditism-mental retardation syndrome, Verloes type", "MALE PSEUDOHERMAPHRODITISM/MENTAL RETARDATION SYNDROME, VERLOES TYPE", "male pseudohermaphroditism/mental retardation syndrome, Verloes type", "Male pseudohermaphroditism intellectual disability syndrome, Verloes type", "male pseudohermaphroditism/intellectual disability syndrome, Verloes type", "Disorder of sex development with intellectual disability syndrome (disorder)", "disorder of sex development with intellectual disability syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of sex development-intellectual disability syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0001493", "names": ["Cor pulmonale", "Cor Pulmonale", "Cor pulmonale chronic", "chronic cor pulmonale", "Chronic cor pulmonale", "COR PULMONALE, CHRONIC", "Chronic Cor pulmonale NOS", "Chronic cor pulmonale, NOS", "COR - Chronic cor pulmonale", "chronic cardiopulmonary disease", "chronic pulmonary heart disease", "Chronic Pulmonary Heart Disease", "Chronic pulmonary heart disease", "Chronic cardiopulmonary disease", "Chronic cor pulmonale (disorder)", "Chronic pulmonary heart disease, NOS", "Other chronic pulmonary heart diseases", "Chronic pulmonary heart disease unspecified", "chronic cardiopulmonary disease (diagnosis)", "Chronic pulmonary heart disease, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic pulmonary heart disease", "shortest_name_length": 13}
{"curie": "MONDO:0014949", "names": ["DEE47", "EIEE47", "early infantile epileptic encephalopathy 47", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 47", "epileptic encephalopathy, early infantile, 47", "developmental and epileptic encephalopathy 47", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 47", "FGF12 early infantile epileptic encephalopathy", "developmental and epileptic encephalopathy, 47", "epileptic encephalopathy, early infantile, type 47", "epileptic encephalopathy, early infantile, 47; EIEE47", "early infantile epileptic encephalopathy caused by mutation in FGF12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 47", "shortest_name_length": 5}
{"curie": "UMLS:C1336233", "names": ["Stage IIIB Squamous Cell Lung Cancer", "Stage IIIB Squamous Cell Lung Carcinoma", "Stage IIIB Squamous Cell Carcinoma of Lung", "Stage IIIB Squamous Cell Carcinoma of the Lung", "Stage IIIB Squamous Cell Lung Carcinoma AJCC v7", "Stage IIIB Lung Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Lung Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 36}
{"curie": "UMLS:C2828099", "names": ["Stage IIIA Vulvar Cancer", "stage IIIA vulvar cancer", "stage IIIA vulvar carcinoma", "Stage IIIA Vulvar Carcinoma", "Stage IIIA Vulvar Cancer AJCC v7", "stage IIIA vulvar cancer AJCC v7", "stage IIIA vulvar carcinoma AJCC v7", "Stage IIIA Vulvar Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Vulvar Cancer AJCC v7", "shortest_name_length": 24}
{"curie": "MONDO:0024264", "names": ["CHNG2", "thyroid, ectopic", "thyroid agenesis", "thyroid dysgenesis", "Thyroid hypoplasia", "Thyroid Hypoplasia", "thyroid hypoplasia", "THYROID HYPOPLASIA", "hypoplasia; thyroid", "Hypoplasia, Thyroid", "thyroid; hypoplasia", "Small thyroid gland", "Hypoplastic thyroid", "Hypoplasia of thyroid", "thyrotropin resistance", "Athyreotic Hypothyroidism", "resistance to thyrotropin", "athyreotic hypothyroidism", "ATHYREOTIC HYPOTHYROIDISM", "hypothyroidism, athyreotic", "HYPOTHYROIDISM, ATHYREOTIC", "Hypothyroidism, Athyreotic", "Hypoplasia of thyroid (disorder)", "congenital nongoitrous hypothyroidism 2", "congenital nongoitrous hypothryoidism 2", "Hypothyroidism, Congenital, Nongoitrous, 2", "hypothyroidism, congenital, nongoitrous, 2", "HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2", "HYPOTHYROIDISM, CONGENITAL, DUE TO THYROID DYSGENESIS", "Hypothyroidism, Congenital, Due To Thyroid Dysgenesis", "hypothyroidism, congenital, due to thyroid dysgenesis", "congenital hypothyroidism due to thyroid dysgenesis or hypoplasia", "hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypothyroidism, congenital, nongoitrous, 2", "shortest_name_length": 5}
{"curie": "MONDO:0015469", "names": ["CRS", "CSO", "craniostosis", "Craniostosis", "Craniostenosis", "craniostenosis", "CRANIOSTENOSIS", "Craniostenoses", "Craniosynostose", "skull deformity", "Craniosyostosis", "SKULL DEFORMITY", "craniosynostosis", "craniosynostoses", "CRANIOSYNOSTOSIS", "skull; deformity", "deformity; skull", "Craniosynostoses", "Craniosynostosis", "CRANIAL DEFORMITY", "deformities skull", "skull abnormality", "Skull deformities", "malformation skull", "MALFORMATION SKULL", "cranial synostosis", "Malformation skull", "skull malformation", "Skull malformation", "abnormalities skull", "cranial deformities", "malformations skull", "synostosis (cranial)", "Skull malformation NOS", "Deformity of the skull", "CSO - Craniosynostosis", "Synostotic Plagiocephaly", "Premature suture closure", "Cranial suture synostosis", "craniosynostosis syndrome", "Craniosynostosis Syndrome", "Craniosynostosis syndrome", "Plagiocephaly, Synostotic", "Isolated craniosynostosis", "Premature fontanel closure", "CRANIOSYNOSTOSIS SYNDROMES", "craniosynostosis syndromes", "craniosynostosis (diagnosis)", "Non-syndromic craniosynostosis", "Craniosynostosis Plagiocephaly", "Early fusion of cranial sutures", "Plagiocephaly, Craniosynostosis", "Premature cranial suture closure", "early closure of cranial sutures", "Congenital ossification of sutures", "skull deformity (physical finding)", "Craniosynostosis syndrome (disorder)", "Premature closure of cranial sutures", "premature closure of cranial sutures", "Early closure of the cranial sutures", "Premature closure of the cranial sutures", "Congenital ossification of cranial sutures", "Congenital ossification of sutures of skull", "early closure of cranial sutures (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniosynostosis", "shortest_name_length": 3}
{"curie": "MONDO:0017140", "names": ["L1 syndrome", "CRASH syndrome", "L1CAM syndrome", "corpus callosum hypoplasia-retardation-adducted thumbs-spasticity-hydrocephalus syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "L1 syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0004537", "names": ["intestinal type mucinous carcinoma", "cervical mucinous adenocarcinoma, intestinal-type", "Cervical Mucinous Adenocarcinoma, Intestinal Type", "Cervical Mucinous Adenocarcinoma, Intestinal-Type", "intestinal variant cervical mucinous adenocarcinoma", "Cervical Mucinous Adenocarcinoma, Intestinal Variant", "cervical mucinous adenocarcinoma, intestinal variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intestinal variant cervical mucinous adenocarcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0031384", "names": ["autoinflammatory syndrome, familial, Behcet-like"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoinflammatory syndrome, familial, Behcet-like", "shortest_name_length": 48}
{"curie": "UMLS:C0866111", "names": ["Nephrotic Syndrome with Lesion of Endothelial Glomerulonephritis", "Nephrotic syndrome with lesion of endothelial glomerulonephritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome with Lesion of Endothelial Glomerulonephritis", "shortest_name_length": 64}
{"curie": "UMLS:C1290049", "names": ["Plaque morphea", "Plaque Morphea", "Plaque morphoea", "Morphea, plaque form", "Plaque morphea (disorder)", "Superficial Circumscribed Morphea"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Plaque morphea", "shortest_name_length": 14}
{"curie": "UMLS:C1336254", "names": ["Stage III Liver Cancer", "Stage III Liver Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Liver Cancer", "shortest_name_length": 22}
{"curie": "MONDO:0018958", "names": ["NM", "NEM", "Rod Myopathy", "rod myopathy", "Rod myopathy", "Myopathy, Rod", "rods; myopathy", "myopathy; rods", "Rod Myopathies", "Myopathies, Rod", "Rod Body Disease", "rod body disease", "Rod body disease", "Nemaline Myopathy", "Rod Body Myopathy", "Nemaline myopathy", "nemaline myopathy", "Rod-body myopathy", "Rod-Body Myopathy", "Myopathy, Rod-Body", "myopathy; nemaline", "nemaline; myopathy", "Myopathy, Nemaline", "Myopathy, Rod Body", "Rod-Body Myopathies", "Nemaline Myopathies", "Myopathies, Rod-Body", "Myopathies, Nemaline", "Nemaline Rod Disease", "nemaline rod disease", "Nemaline body disease", "Nemaline rod myopathy", "nemaline body disease", "Nemaline Body Disease", "nemaline rod myopathy", "congenital rod disease", "Nemaline myopathy (disorder)", "nemaline body disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nemaline myopathy", "shortest_name_length": 2}
{"curie": "MONDO:0017344", "names": ["EBV-associated carcinoma", "Epstein-Barr virus-associated carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epstein-Barr virus-associated carcinoma", "shortest_name_length": 24}
{"curie": "MONDO:0002030", "names": ["chronic cervicitis", "Chronic Cervicitis", "Chronic cervicitis", "cervicitis chronic", "chronic cervicitis (disease)", "Chronic cervicitis (disorder)", "cervicitis (disease), chronic", "Chronic cervicitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic cervicitis", "shortest_name_length": 18}
{"curie": "UMLS:C0236167", "names": ["IUD complication", "complication iud", "IUD COMPLICATION", "complications iud", "complications; IUD", "IUD; complications", "Intrauterine Device Complication", "INTRA-UTERINE DEVICE COMPLICATION", "intra-uterine device complication", "contraceptive; complications, intrauterine", "complications; contraceptive, intrauterine", "Intrauterine contraceptive device complication", "complications; intrauterine contraceptive device"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "INTRA-UTERINE DEVICE COMPLICATION", "shortest_name_length": 16}
{"curie": "MONDO:0019781", "names": ["ASTROCYTOMA", "Astroglioma", "Astrocytoma", "astrocytoma", "astroglioma", "Astrogliomas", "astrocytomas", "astrogliomas", "Astrocytomas", "Astrocytoma NOS", "Astrocytic tumor", "Astrocytic Tumor", "Astrocytoma, NOS", "Astrocytic Glioma", "astrocytic glioma", "Astrocytic glioma", "Astrocytic Gliomas", "[M]Astrocytoma NOS", "Glioma, Astrocytic", "Gliomas, Astrocytic", "Astrocytic Neoplasm", "astrocytoma (excluding glioblastoma)", "Astrocytoma (morphologic abnormality)", "Primary malignant astrocytoma of central nervous system", "Primary malignant astrocytoma of central nervous system (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "astrocytoma (excluding glioblastoma)", "shortest_name_length": 11}
{"curie": "UMLS:C5419974", "names": ["Digestive System Rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Digestive System Rhabdomyosarcoma", "shortest_name_length": 33}
{"curie": "MONDO:0003558", "names": ["adenosquamous prostate carcinoma", "Prostate Adenosquamous Carcinoma", "prostate adenosquamous carcinoma", "Adenosquamous Carcinoma of Prostate", "adenosquamous carcinoma of prostate", "prostate gland adenosquamous carcinoma", "Adenosquamous Carcinoma of the Prostate", "adenosquamous carcinoma of the prostate", "Adenosquamous carcinoma of the prostate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenosquamous prostate carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0003591", "names": ["renal liposarcoma", "Renal Liposarcoma", "Kidney Liposarcoma", "kidney liposarcoma", "liposarcoma of kidney", "Liposarcoma of Kidney", "Liposarcoma of kidney", "Liposarcoma of the Kidney", "liposarcoma of the kidney", "liposarcoma of kidney (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kidney liposarcoma", "shortest_name_length": 17}
{"curie": "MONDO:0001734", "names": ["TSC", "Epiloia", "adenoma sebaceum", "Tuberous sclerosis", "Tuberose sclerosis", "tuberose sclerosis", "cerebral Scleroses", "sclerosis Tuberosa", "Tuberous Sclerosis", "cerebral sclerosis", "tuberous sclerosis", "Bourneville disease", "sclerosis, tuberous", "sclerosis, cerebral", "sclerosis, tuberose", "Bourneville syndrome", "Bourneville's disease", "syndrome, Bourneville", "bourneville's disease", "Bourneville's Disease", "Bourneville's syndrome", "syndrome, Bourneville's", "ts - tuberous sclerosis", "Bourneville Phacomatosis", "Bourneville phakomatosis", "Phacomatosis, Bourneville", "adenoma sebaceum syndrome", "phakomatosis, Bourneville", "Tuberous Sclerosis Complex", "tuberous sclerosis complex", "tuberous sclerosis Complex", "Tuberous sclerosis syndrome", "Tuberous Sclerosis Syndrome", "Bourneville pringle disease", "tuberous sclerosis syndrome", "Bourneville-pringle disease", "disease, Bourneville-pringle", "Bourneville-Pringles disease", "Bourneville pringle's disease", "Bourneville-pringle's disease", "disease, Bourneville-pringle's"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tuberous sclerosis", "shortest_name_length": 3}
{"curie": "UMLS:C1335365", "names": ["Parotid Non-Hodgkin's Lymphoma", "Non-Hodgkin's Lymphoma of Parotid", "Parotid Gland Non-Hodgkin Lymphoma", "Parotid Gland Non-Hodgkin's Lymphoma", "Non-Hodgkin's Lymphoma of the Parotid", "Non-Hodgkin's Lymphoma of Parotid Gland", "Primary Parotid Gland Non-Hodgkin Lymphoma", "Non-Hodgkin's Lymphoma of the Parotid Gland", "Primary Parotid Gland Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parotid Gland Non-Hodgkin Lymphoma", "shortest_name_length": 30}
{"curie": "MONDO:0001569", "names": ["Acoustic Tumor", "acoustic tumor", "Acoustic Tumors", "Tumor, Acoustic", "acoustic neuroma", "Acoustic neuroma", "Tumors, Acoustic", "ACOUSTIC NEUROMA", "Acoustic Neuroma", "Neuroma;acoustic", "acoustic neuromas", "neuroma, acoustic", "Neuroma, Acoustic", "NEUROMA, ACOUSTIC", "Acoustic Neuromas", "Acoustic neurinoma", "acoustic neuroma -", "Neuromas, Acoustic", "Acoustic Neurinoma", "acoustic neurinoma", "acoustic; neurinoma", "Acoustic Neurinomas", "Acoustic Schwannoma", "acoustic schwannoma", "Acoustic schwannoma", "Neurinoma, Acoustic", "NEURINOMA, ACOUSTIC", "Acoustic Neurilemoma", "Vestibular neurinoma", "Acoustic Schwannomas", "Schwannoma, Acoustic", "Neurinomas, Acoustic", "Acoustic neurilemoma", "acoustic neurilemoma", "neurilemoma, acoustic", "Vestibular Schwannoma", "vestibular schwannoma", "Neurilemoma, Acoustic", "Schwannomas, Acoustic", "Acoustic Neurilemmoma", "Vestibular schwannoma", "schwannoma vestibular", "AN - Acoustic neuroma", "acoustic neurilemmoma", "Acoustic Neurilemomas", "Acoustic neurilemmoma", "NEUROFIBROMA, ACOUSTIC", "Acoustic Neurilemmomas", "vestibular schwannomas", "Vestibular Schwannomas", "Neurilemomas, Acoustic", "Neurilemmoma, Acoustic", "Schwannoma, Vestibular", "Vestibular neurolemmoma", "vestibular neurilemmoma", "Neurilemmomas, Acoustic", "Vestibular neurilemmoma", "Schwannomas, Vestibular", "Vestibular Neurilemmoma", "Acoustic neuroma (disorder)", "acoustic neuroma brain tumor", "Vestibular Schwann cell tumor", "BRAIN TUMOR, ACOUSTIC NEUROMA", "Vestibular Schwann cell tumour", "Neurinoma of the Acoustic Nerve", "vestibular schwannoma (disease)", "neurinoma of the acoustic nerve", "INTRACRANIAL NEOPLASM, ACOUSTIC NEUROMA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acoustic neuroma", "shortest_name_length": 14}
{"curie": "UMLS:C4055250", "names": ["Childhood AML with Abnormalities of Chromosome 5q", "Acute Myeloid Leukemia (AML) with Abnormalities of Chromosome 5q", "Childhood Acute Myeloid Leukemia with Abnormalities of Chromosome 5q"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Acute Myeloid Leukemia with Abnormalities of Chromosome 5q", "shortest_name_length": 49}
{"curie": "MONDO:0011594", "names": ["OVARIAN DYSGENESIS, HYPERGONADOTROPIC, WITH SHORT STATURE AND RECURRENT METABOLIC ACIDOSIS", "ovarian dysgenesis, hypergonadotropic, with short stature and recurrent metabolic acidosis", "Gonadal Dysgenesis, Hypergonadotropic, XX Type, Short Stature, and Recurrent Metabolic Acidosis", "gonadal dysgenesis, hypergonadotropic, 20 type, with short stature and recurrent metabolic acidosis", "GONADAL DYSGENESIS, HYPERGONADOTROPIC, XX TYPE, WITH SHORT STATURE AND RECURRENT METABOLIC ACIDOSIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian dysgenesis, hypergonadotropic, with short stature and recurrent metabolic acidosis", "shortest_name_length": 90}
{"curie": "UMLS:C5447320", "names": ["Immune Dysregulation Disorder", "Diseases of Immune Dysregulation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immune Dysregulation Disorder", "shortest_name_length": 29}
{"curie": "MONDO:0021929", "names": ["Localised myositis ossificans", "traumatic myositis ossificans", "Traumatic Myositis Ossificans", "Traumatic myositis ossificans", "Localized myositis ossificans", "MYOSITIS OSSIFICANS, TRAUMATIC", "myositis ossificans traumatica", "Myositis ossificans traumatica", "myositis; ossificans, traumatic", "muscle; calcification, traumatic", "Traumatic myositis ossifications", "calcification; muscle, traumatic", "Myisitis ossificans circumscripta", "myositis ossificans circumscripta", "Myositis ossificans circumscripta", "Traumatic myositis ossificans (disorder)", "traumatic myositis ossificans (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "traumatic myositis ossificans", "shortest_name_length": 29}
{"curie": "MONDO:0011509", "names": ["LDLC, MILD ELEVATION OF", "Ldlc, mild elevation of", "low density lipoprotein cholesterol, mild elevation of", "LOW DENSITY LIPOPROTEIN CHOLESTEROL, MILD ELEVATION OF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "low density lipoprotein cholesterol, mild elevation of", "shortest_name_length": 23}
{"curie": "UMLS:C1333373", "names": ["Ectopic Meningioma", "Primary Ectopic Meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ectopic Meningioma", "shortest_name_length": 18}
{"curie": "MONDO:0000968", "names": ["Renal Lipoma", "Renal lipoma", "renal lipoma", "kidney lipoma", "Kidney Lipoma", "Lipoma of Kidney", "Lipoma of kidney", "lipoma of kidney", "Lipoma of the Kidney", "lipoma of the kidney"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kidney lipoma", "shortest_name_length": 12}
{"curie": "UMLS:C5420079", "names": ["Nasal Cavity Extranodal NK/T-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasal Cavity Extranodal NK/T-Cell Lymphoma", "shortest_name_length": 42}
{"curie": "UMLS:C0524948", "names": ["Maxillofacial Abnormality", "Abnormality, Maxillofacial", "Maxillofacial Abnormalities", "Abnormalities, Maxillofacial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Maxillofacial Abnormalities", "shortest_name_length": 25}
{"curie": "MONDO:0014406", "names": ["PAGEN2", "PANCREATIC AGENESIS 2", "pancreatic agenesis 2", "PTF1A pancreatic agenesis", "pancreatic agenesis type 2", "pancreatic hypoplasia, congenital 2", "PANCREATIC HYPOPLASIA, CONGENITAL 2", "pancreatic agenesis caused by mutation in PTF1A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic agenesis 2", "shortest_name_length": 6}
{"curie": "UMLS:C4038767", "names": ["Gastric hemorrhage due to angiodysplasia of stomach", "gastric hemorrhage due to angiodysplasia of stomach", "Gastric haemorrhage due to angiodysplasia of stomach", "Gastric hemorrhage due to angiodysplasia of stomach (disorder)", "gastric hemorrhage due to angiodysplasia of stomach (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric hemorrhage due to angiodysplasia of stomach", "shortest_name_length": 51}
{"curie": "MONDO:0011684", "names": ["VTLG", "SLEV1", "VAMAS1", "VITILIGO", "vitiligo", "systemic lupus erythematosus, vitiligo-related", "SYSTEMIC LUPUS ERYTHEMATOSUS, VITILIGO-RELATED", "vitiligo-associated multiple autoimmune disease susceptibility 1", "VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1", "vitiligo-associated multiple autoimmune disease susceptibility type 1", "VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitiligo-associated multiple autoimmune disease susceptibility 1", "shortest_name_length": 4}
{"curie": "UMLS:C4725785", "names": ["Small Intestinal Monomorphic Epitheliotropic T-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Intestinal Monomorphic Epitheliotropic T-Cell Lymphoma", "shortest_name_length": 60}
{"curie": "MONDO:0030105", "names": ["GALAC4", "galactosemia 4", "galactosemia iv", "GALM deficiency", "GALACTOSEMIA IV", "Galactosemia type 4", "Galactosaemia type 4", "GALM mutarotase deficiency", "GALACTOSE MUTAROTASE DEFICIENCY", "Galactose Mutarotase Deficiency", "Galactose mutarotase deficiency", "Deficiency of galactose mutarotase", "GALM (galactose mutarotase) deficiency", "Deficiency of galactose mutarotase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "galactosemia 4", "shortest_name_length": 6}
{"curie": "UMLS:C1709241", "names": ["Nonfunctional Pancreatic Neuroendocrine Tumor G2", "Nonfunctioning Pancreatic Neuroendocrine Tumor G2", "Non-Functional Pancreatic Neuroendocrine Tumor G2", "Non-Functioning Pancreatic Neuroendocrine Tumor G2", "Non-Functioning Well Differentiated Pancreatic Endocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Functioning Pancreatic Neuroendocrine Tumor G2", "shortest_name_length": 48}
{"curie": "UMLS:C4764238", "names": ["Metastatic Salivary Gland Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Salivary Gland Carcinoma", "shortest_name_length": 35}
{"curie": "MONDO:0040871", "names": ["Primary polydipsia", "Primary Polydipsia", "primary polydipsia", "Primary Polydipsias", "Polydipsia, Primary", "Polydipsias, Primary", "Psychogenic Polydipsia", "Polydipsia psychogenic", "polydipsia psychogenic", "psychogenic polydipsia", "PSYCHOGENIC POLYDIPSIA", "Psychogenic polydipsia", "Polydipsia, Psychogenic", "Psychogenic Polydipsias", "Polydipsias, Psychogenic", "compulsive water drinking", "psychogenic water drinking", "Psychogenic polydipsia (disorder)", "psychogenic water drinking (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "psychogenic polydipsia", "shortest_name_length": 18}
{"curie": "MONDO:0013896", "names": ["JBTS18", "Joubert syndrome 18", "JOUBERT SYNDROME 18", "TCTN3 Joubert syndrome", "Joubert syndrome type 18", "Joubert syndrome caused by mutation in TCTN3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome 18", "shortest_name_length": 6}
{"curie": "MONDO:0032938", "names": ["IBGC8", "BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 8, AUTOSOMAL RECESSIVE", "basal ganglia calcification, idiopathic, 8, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "basal ganglia calcification, idiopathic, 8, autosomal recessive", "shortest_name_length": 5}
{"curie": "UMLS:C0039232", "names": ["AV nodal re-entry tachycardia", "AV nodal reentrant tachycardia", "AV Nodal Reentrant Tachycardia", "A-V nodal re-entry tachycardia", "Tachycardia, AV Nodal Reentrant", "Atrioventricular Reentrant Tachycardia", "Reentrant Tachycardia, Atrioventricular", "Tachycardia, Atrioventricular Reentrant", "Atrioventricular Reentrant Tachycardias", "Atrioventricular Nodal Reentry Tachycardia", "Tachycardia, Atrioventricular Nodal Reentry", "Atrioventricular nodal re-entry tachycardia", "atrioventricular nodal re-entry tachycardia", "Atrioventricular nodal reentrant tachycardia", "Atrioventricular Nodal Reentrant Tachycardia", "Atrioventricular Nodal Re Entrant Tachycardia", "Atrioventricular Nodal Re-Entrant Tachycardia", "SUPRAVENTRICULAR TACHYCARDIA AV NODE REENTRANT", "Atrioventricular nodal re-entry tachycardia (disorder)", "atrioventricular nodal re-entry tachycardia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tachycardia, Atrioventricular Nodal Reentry", "shortest_name_length": 29}
{"curie": "MONDO:0009979", "names": ["Reticular dystrophy of retinal pigment epithelium", "reticular dystrophy of retinal pigment epithelium", "RETICULAR DYSTROPHY OF RETINAL PIGMENT EPITHELIUM", "Reticular Dystrophy Of Retinal Pigment Epithelium", "reticular dystrophy of the retinal pigment epithelium", "Reticular dystrophy of the retinal pigment epithelium", "retinal dystrophy, reticular pigmentary, of POSTERIOR POLE", "Reticular dystrophy of retinal pigment epithelium (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "reticular dystrophy of the retinal pigment epithelium", "shortest_name_length": 49}
{"curie": "MONDO:0015157", "names": ["HHV-8-related disorder", "human herpesvirus 8-related tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "human herpesvirus 8-related tumor", "shortest_name_length": 22}
{"curie": "UMLS:C1698099", "names": ["Intraoperative splenic injury", "intraoperative splenic injury", "Intraoperative Splenic Injury", "intraoperative splenic injury (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraoperative Splenic Injury", "shortest_name_length": 29}
{"curie": "UMLS:C1112677", "names": ["protein allergy", "Protein allergy", "allergy protein", "allergies protein", "allergies proteins"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Protein allergy", "shortest_name_length": 15}
{"curie": "UMLS:C0240392", "names": ["Mucous Membrane Hemangioma", "MUCOUS MEMBRANE HEMANGIOMA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mucous Membrane Hemangioma", "shortest_name_length": 26}
{"curie": "UMLS:C0161408", "names": ["VIIth nerve injury", "n.facialis; injury", "Facial Nerve Injury", "Facial nerve injury", "facial nerve injury", "Facial Nerve Trauma", "Nerve Injury, Facial", "Facial Nerve Traumas", "Injury, Facial Nerve", "Nerve Trauma, Facial", "injury; facial nerve", "Trauma, Facial Nerve", "Facial Nerve Injuries", "Injury of facial nerve", "Injury to facial nerve", "Facial (7th) nerve injury", "Cranial Nerve VII Injuries", "Traumatic facial neuropathy", "Traumatic Facial Neuropathy", "Injuries, Cranial Nerve VII", "Neuropathy, Traumatic Facial", "Seventh cranial nerve injury", "Facial Neuropathy, Traumatic", "Traumatic Facial Neuropathies", "traumatic facial nerve injury", "Seventh Cranial Nerve Injuries", "Injury to seventh cranial nerve", "Injuries, Seventh Cranial Nerve", "facial nerve injury (diagnosis)", "Injury of seventh cranial nerve", "Injury of facial nerve (disorder)", "traumatic facial nerve injury (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Facial Nerve Injuries", "shortest_name_length": 18}
{"curie": "MONDO:0014276", "names": ["IMD17", "CD3 deficiency", "CD3gamma deficiency", "immunodeficiency 17", "IMMUNODEFICIENCY 17", "CD3-GAMMA DEFICIENCY", "CD3-gamma deficiency", "immunodeficiency type 17", "immunodeficiency 17, CD3 gamma deficient", "Combined immunodeficiency due to CD3gamma deficiency", "combined immunodeficiency due to CD3gamma deficiency", "Combined immunodeficiency due to CD3-gamma deficiency", "Combined immunodeficiency due to CD3gamma deficiency (disorder)", "Combined immunodeficiency due to CD3gamma deficiency (diagnosis)", "SCID-LIKE IMMUNODEFICIENCY, T CELL-PARTIAL, B CELL-POSITIVE, NK CELL-POSITIVE", "SCID-like immunodeficiency, T cell-partial, B cell-positive, NK cell-positive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined immunodeficiency due to CD3gamma deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C5237968", "names": ["Locally Advanced Rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Rhabdomyosarcoma", "shortest_name_length": 33}
{"curie": "MONDO:0001664", "names": ["submucous uterine fibroid", "Submucous uterine fibroid", "submucous uterine leiomyoma", "Submucous uterine leiomyoma", "leiomyoma; uterus, submucous", "uterus; leiomyoma, submucous", "Submucous leiomyoma of uterus", "submucous leiomyoma of uterus", "Submucous leiomyoma of uterus (disorder)", "submucous leiomyoma of uterus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "submucous uterine fibroid", "shortest_name_length": 25}
{"curie": "MONDO:0001513", "names": ["exophthalmos pulsating", "Pulsating exophthalmos", "pulsating exophthalmos", "exophthalmos; pulsating", "pulsating; exophthalmos", "Pulsating exophthalmos (disorder)", "Pulsating exophthalmos (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulsating exophthalmos", "shortest_name_length": 22}
{"curie": "UMLS:C0242073", "names": ["congestion lung", "Congestive lung", "Lung congestion", "lung congestion", "Congestion;chest", "congestion lungs", "congestive; lung", "Chest congestion", "CHEST CONGESTION", "congestion chest", "lung; congestive", "congestion; lung", "chest congestion", "congestion pulmonary", "Congestion pulmonary", "PULMONARY CONGESTION", "pulmonary congestion", "Pulmonary congestion", "CONGESTION PULMONARY", "congestion; pulmonary", "Pulmonary congestion, NOS", "Pulmonary congestion (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pulmonary congestion", "shortest_name_length": 15}
{"curie": "MONDO:0003582", "names": ["HBOC syndrome", "syndrome, HBOC", "HBOC syndromes", "syndromes, HBOC", "hereditary breast ovarian cancer", "hereditary breast and ovarian cancer", "hereditary breast ovarian cancer syndrome", "familial breast and ovarian cancer syndrome", "hereditary breast and ovarian cancer syndrome", "familial breast/ovarian cancer (BRCA1, BRCA2)", "hereditary breast/ovarian cancer (BRCA1, BRCA2)", "breast-ovarian cancer, familial, susceptibility to", "BRCA1- and BRCA2-associated hereditary breast and ovarian cancer", "BRCA1- and BRCA2-associated hereditary breast and ovarian cancer (HBOC)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary breast ovarian cancer syndrome", "shortest_name_length": 13}
{"curie": "UMLS:C1336378", "names": ["Stage IVB Salivary Gland Cancer", "Stage IVB Major Salivary Gland Cancer", "Stage IVB Major Salivary Gland Carcinoma", "Stage IVB Major Salivary Gland Cancer AJCC v7", "Stage IVB Major Salivary Gland Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Major Salivary Gland Cancer AJCC v7", "shortest_name_length": 31}
{"curie": "UMLS:C1520102", "names": ["Vulvar Warty Carcinoma", "Vulvar Condylomatous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Warty Carcinoma", "shortest_name_length": 22}
{"curie": "UMLS:C4721748", "names": ["Stage IV Esophagus Adenocarcinoma", "Stage IV Esophageal Adenocarcinoma", "Oesophageal Adenocarcinoma Stage IV", "Esophageal Adenocarcinoma, Stage IV", "Stage IV Adenocarcinoma of Esophagus", "Stage IV Adenocarcinoma of the Esophagus", "Stage IV Esophageal Adenocarcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Esophageal Adenocarcinoma AJCC v7", "shortest_name_length": 33}
{"curie": "UMLS:C4086147", "names": ["Celosomy", "CELOSOMY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Celosomy", "shortest_name_length": 8}
{"curie": "MONDO:0001222", "names": ["T cell deficiency", "T lymphocyte deficiency", "T cell immunodeficiency", "T lymphocyte immunodeficiency", "Congenital T-Cell Immunodeficiency", "congenital T-cell immunodeficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital T-cell immunodeficiency", "shortest_name_length": 17}
{"curie": "UMLS:C1266001", "names": ["Tumorlet", "Tumorlet, NOS", "Benign Tumorlet", "Tumorlet, benign", "Tumourlet, benign", "Tumorlet, benign (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tumorlet, benign", "shortest_name_length": 8}
{"curie": "UMLS:C1708566", "names": ["Invasive Prostate Cancer", "Invasive Prostate Carcinoma", "Infiltrating Prostate Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Invasive Prostate Carcinoma", "shortest_name_length": 24}
{"curie": "MONDO:0002962", "names": ["epidermolytic acanthoma", "Epidermolytic Acanthoma", "Epidermolytic acanthoma", "Epidermolytic acanthoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolytic acanthoma", "shortest_name_length": 23}
{"curie": "MONDO:0012000", "names": ["simple phobia", "PHOBIA SIMPLE", "phobia simple", "Simple phobia", "phobia; simple", "PHOBIA, SIMPLE", "phobias simple", "Phobia, Simple", "simple; phobia", "phobia, simple", "specific phobia", "Isolated phobia", "Specific Phobia", "Specific phobia", "phobia; specific", "Specific phobias", "Phobia, Specific", "phobias specific", "phobia, specific", "specific; phobia", "PHOBIA, SPECIFIC", "simple (specific) phobia", "Simple phobia (disorder)", "Specific (isolated) phobias", "specific phobia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "specific phobia", "shortest_name_length": 13}
{"curie": "UMLS:C0235504", "names": ["THROMBOPHLEBITIS LEG", "Thrombophlebitis leg", "leg; thrombophlebitis", "thrombophlebitis; leg", "Thrombophlebitis of the leg"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thrombophlebitis leg", "shortest_name_length": 20}
{"curie": "MONDO:0006250", "names": ["Ileal NET G1", "ileal NET G1", "ileum NET G1", "Ileal Carcinoid Tumor", "ILEAL CARCINOID TUMOR", "ileum carcinoid tumor", "ileal carcinoid tumor", "carcinoid tumor of ileum", "Carcinoid Tumor of Ileum", "Carcinoid tumor of ileum", "Carcinoid tumour of ileum", "carcinoid tumor of the ileum", "Carcinoid Tumor of the Ileum", "ileal neuroendocrine tumor G1", "Ileal Neuroendocrine Tumor G1", "ileum carcinoid tumor (disease)", "ileum neuroendocrine neoplasm G1", "Carcinoid tumor of ileum (disorder)", "grade 1 neuroendocrine neoplasm of ileum", "ileum neuroendocrine tumor, well differentiated, low grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ileal neuroendocrine tumor G1", "shortest_name_length": 12}
{"curie": "MONDO:0002186", "names": ["acute antritis", "Acute antritis", "antritis; acute", "acute; antritis", "acute maxillary sinusitis", "MAXILLARY SINUSITIS ACUTE", "Acute maxillary sinusitis", "Acute sinusitis, maxillary", "maxillary sinusitis, acute", "sinusitis; acute, maxillary", "maxillary; sinusitis, acute", "sinusitis; maxillary, acute", "acute; sinusitis, maxillary", "Acute maxillary sinusitis (disorder)", "acute maxillary sinusitis (diagnosis)", "Acute maxillary sinusitis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute maxillary sinusitis", "shortest_name_length": 14}
{"curie": "UMLS:C0855228", "names": ["Disordered Eating", "disordered eating", "Eating disorder symptom", "Eating disorder symptoms", "disordered eating (symptom)", "Eating disorder symptom NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eating disorder symptom", "shortest_name_length": 17}
{"curie": "MONDO:0000965", "names": ["liver lipoma", "Liver Lipoma", "Hepatic Lipoma", "Hepatic lipoma", "hepatic lipoma", "lipoma of liver", "Lipoma of Liver", "Lipoma of the Liver", "lipoma of the liver"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "liver lipoma", "shortest_name_length": 12}
{"curie": "UMLS:C0920561", "names": ["Infection-Related Cancer", "infection related cancer", "Infection Related Cancer", "Infection-Related Malignancy", "Infection Related Malignancy", "Infection-Related Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infection-Related Malignant Neoplasm", "shortest_name_length": 24}
{"curie": "UMLS:C1335030", "names": ["Non-Neoplastic Peritoneal Disease", "Non-Neoplastic Peritoneal Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Peritoneal Disorder", "shortest_name_length": 33}
{"curie": "UMLS:C4763994", "names": ["PEComa of the Kidney", "Renal Epithelioid Angiomyolipoma", "Kidney Epithelioid Angiomyolipoma", "Kidney Epithelioid Type Angiomyolipoma", "Perivascular Epithelioid Cell Tumor of the Kidney"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kidney Epithelioid Angiomyolipoma", "shortest_name_length": 20}
{"curie": "UMLS:C0561852", "names": ["bone injury", "Bone injury", "Bone Injury", "bone injuries", "injury of bone", "BI - Bone injury", "bone disorder injury", "Bone injury (disorder)", "Bone injury (diagnosis)", "bone disorders injuries", "injury of bone (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone injury", "shortest_name_length": 11}
{"curie": "MONDO:0014400", "names": ["RP70", "RETINITIS PIGMENTOSA 70", "retinitis pigmentosa 70", "PRPF4 retinitis pigmentosa", "retinitis pigmentosa type 70", "retinitis pigmentosa caused by mutation in PRPF4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 70", "shortest_name_length": 4}
{"curie": "UMLS:C1285519", "names": ["Metanephric Stromal Tumor", "Metanephric stromal tumor", "Metanephric stromal tumour", "Metanephric stromal tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metanephric stromal tumor", "shortest_name_length": 25}
{"curie": "UMLS:C2981268", "names": ["Stage II Differentiated Thyroid Gland Cancer", "Stage II Differentiated Thyroid Gland Carcinoma", "Stage II Differentiated Thyroid Gland Carcinoma AJCC v7", "Stage II Thyroid Gland Papillary or Follicular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Differentiated Thyroid Gland Carcinoma AJCC v7", "shortest_name_length": 44}
{"curie": "MONDO:0016433", "names": ["Dysmorphism-short stature-deafness-pseudohermaphroditism syndrome", "dysmorphism-short stature-deafness-disorder of sex development syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dysmorphism-short stature-deafness-disorder of sex development syndrome", "shortest_name_length": 65}
{"curie": "UMLS:C3272973", "names": ["Anal Papillary Hidradenoma", "Anal Hidradenoma Papilliferum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anal Hidradenoma Papilliferum", "shortest_name_length": 26}
{"curie": "UMLS:C1332299", "names": ["Angiosarcoma NCI Grade 3", "Angiosarcoma NCI Grade III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Angiosarcoma NCI Grade 3", "shortest_name_length": 24}
{"curie": "MONDO:0016539", "names": ["atypical HCS", "atypical hypotonia-cystinuria syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical hypotonia-cystinuria syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0017210", "names": ["infectious anterior uveitis", "Infectious anterior uveitis", "Secondary infected iridocyclitis", "secondary infected iridocyclitis", "infectious secondary iridocyclitis", "iridocyclitis secondary infectious", "secondary infectious iridocyclitis", "Secondary infectious iridocyclitis", "Infectious secondary iridocyclitis", "secondary iridocyclitis, infectious", "Secondary iridocyclitis, infectious", "Secondary infected iridocyclitis (disorder)", "Infectious secondary iridocyclitis (disorder)", "secondary infectious iridocyclitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infectious anterior uveitis", "shortest_name_length": 27}
{"curie": "UMLS:C1332141", "names": ["Acroparesthesia Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acroparesthesia Syndrome", "shortest_name_length": 24}
{"curie": "UMLS:C0677898", "names": ["invasive cancer", "cancers invasive", "infiltrating cancer", "cancer infiltrating", "Invasive Malignant Neoplasm", "Infiltrating Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Invasive Malignant Neoplasm", "shortest_name_length": 15}
{"curie": "MONDO:0020607", "names": ["LIDLS1", "Liddle syndrome", "Liddle syndrome 1", "Pseudoaldosteronism", "SCNN1B Liddle syndrome", "Liddle syndrome caused by mutation in SCNN1B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liddle syndrome 1", "shortest_name_length": 6}
{"curie": "UMLS:C4264446", "names": ["Mixed carcinoma", "Mixed Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mixed Carcinoma", "shortest_name_length": 15}
{"curie": "UMLS:C1699740", "names": ["Intraoperative ocular injury", "Intraoperative Ocular Injury", "intraoperative ocular injury", "intraoperative ocular injury (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraoperative Ocular Injury", "shortest_name_length": 28}
{"curie": "MONDO:0018308", "names": ["MHL", "VMC", "Liver MH", "liver MH", "Biliary hamartoma", "biliary hamartoma", "Von Meyenburg complex", "von Meyenburg complex", "Von Meyenburg complexes", "hepatic cystic hamartoma", "Hepatic cystic hamartoma", "Liver Mesenchymal Hamartoma", "liver mesenchymal hamartoma", "Multiple biliary hamartomas", "Multiple bile duct hamartomas", "hepatic mesenchymal hamartoma", "Hepatic Mesenchymal Hamartoma", "Mesenchymal hamartoma of liver", "Mesenchymal Hamartoma of Liver", "mesenchymal hamartoma of liver", "Von Meyenburg complexes disease", "mesenchymal hamartoma of the liver", "Mesenchymal Hamartoma of the Liver", "Mesenchymal hamartoma of liver (disorder)", "Biliary hamartoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "liver mesenchymal hamartoma", "shortest_name_length": 3}
{"curie": "MONDO:0030300", "names": ["CMD2D", "dilated cardiomyopathy 2D", "cardiomyopathy, dilated, 2D", "CARDIOMYOPATHY, DILATED, 2D"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiomyopathy, dilated, 2D", "shortest_name_length": 5}
{"curie": "UMLS:C1168199", "names": ["gallbladder cancer stage IVA", "Stage IVA Gallbladder Cancer", "stage IVA gallbladder cancer", "Stage IVA Gallbladder Carcinoma", "gallbladder carcinoma stage IVA", "stage IVA carcinoma of gallbladder", "Stage IVA Gallbladder Cancer AJCC v7", "stage IVA gallbladder cancer AJCC v7", "Gallbladder Cancer Stage IVA AJCC v7", "stage IVA carcinoma of the gallbladder", "Stage IVA Gallbladder Carcinoma AJCC v7", "Gallbladder Carcinoma Stage IVA AJCC v7", "Stage IVA Carcinoma of Gallbladder AJCC v7", "Stage IVA Carcinoma of the Gallbladder AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Gallbladder Carcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0024350", "names": ["Pityriasis steatoides", "pityriasis steatoides", "Pityriasis steatoides (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pityriasis steatoides", "shortest_name_length": 21}
{"curie": "MONDO:0044907", "names": ["metastatic squamous cell carcinoma", "Metastatic Squamous Cell Carcinoma", "squamous cell carcinoma metastatic", "SQUAMOUS CELL CARCINOMA METASTATIC", "Metastatic squamous cell carcinoma", "Squamous cell carcinoma, metastatic", "Squamous cell carcinoma, metastatic NOS", "Squamous cell carcinoma, metastatic, NOS", "Metastatic squamous cell carcinoma (disorder)", "Squamous cell carcinoma, metastatic (diagnosis)", "Squamous cell carcinoma, metastatic (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metastatic squamous cell carcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0000820", "names": ["CCM", "brain cavernous hemangioma", "familial cavernous angioma", "Cerebral Cavernous Malformation", "cerebral cavernous malformation", "cerebral capillary malformations", "cavernous angiomatous malformations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral cavernous malformation", "shortest_name_length": 3}
{"curie": "MONDO:0001565", "names": ["abnormal retinal correspondence", "Abnormal retinal correspondence", "retinal; correspondence abnormal", "abnormal; retinal correspondence", "Anomalous retinal correspondence", "ARC - Abnormal retinal correspondence", "Abnormal retinal correspondence (disorder)", "abnormal retinal correspondence (diagnosis)", "Binocular vision, abnormal retinal correspondence"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "abnormal retinal correspondence", "shortest_name_length": 31}
{"curie": "MONDO:0007690", "names": ["AEXS", "GYNECOMASTIA, HEREDITARY", "gynecomastia, hereditary", "Gynecomastia, Hereditary", "Aromatase excess syndrome", "AROMATASE EXCESS SYNDROME", "Aromatase Excess Syndrome", "familial hyperestrogenism", "aromatase excess syndrome", "Familial hyperestrogenism", "Increased aromatase activity", "increased aromatase activity", "aromatase activity, increased", "AROMATASE ACTIVITY, INCREASED", "Estrogen synthetase deficiency", "Oestrogen synthetase deficiency", "Hereditary prepubertal gynecomastia", "hereditary prepubertal gynecomastia", "Aromatase excess syndrome (disorder)", "familial gynecomastia, due to increased aromatase activity", "Gynecomastia, Familial, due to Increased Aromatase Activity", "gynecomastia, familial, due to increased aromatase activity", "GYNECOMASTIA, FAMILIAL, DUE TO INCREASED AROMATASE ACTIVITY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aromatase excess syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0010512", "names": ["MRXSB", "mental retardation, X-linked, syndromic, Bain type", "MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE", "intellectual disability, X-linked, syndromic, Bain type", "Bain Type of X-linked Syndromic Intellectual Disability", "Intellectual Developmental Disorder, X-linked, Syndromic, Bain Type", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, BAIN TYPE", "intellectual developmental disorder, X-linked, syndromic, Bain type, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked, syndromic, Bain type", "shortest_name_length": 5}
{"curie": "MONDO:0019895", "names": ["monosomy 4qter", "distal monosomy 4q", "distal deletion 4q", "telomeric deletion 4q", "distal monosomy type 4q"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal monosomy 4q", "shortest_name_length": 14}
{"curie": "MONDO:0032887", "names": ["NEDMCMS", "Vandervore-Schot Syndrome", "VANDERVORE-SCHOT SYNDROME", "NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CORTICAL MALFORMATIONS, AND SPASTICITY", "neurodevelopmental disorder with microcephaly, cortical malformations, and spasticity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with microcephaly, cortical malformations, and spasticity", "shortest_name_length": 7}
{"curie": "MONDO:0012830", "names": ["Del(10)(q22.3q23.3)", "monosomy 10q22.3q23.3", "deletion 10q22.3q23.3", "juvenile polyposis of infancy", "juvenile polyposis, infantile", "10q22.3q23 microdeletion syndrome", "chromosome 10q23 deletion syndrome", "Chromosome 10q23 Deletion Syndrome", "10q22.3q23.3 microdeletion syndrome", "chromosome 10q22.3-q23.2 deletion syndrome", "chromosome 10Q22.3-q23.2 deletion syndrome", "CHROMOSOME 10q22.3-q23.2 DELETION SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 10q23 deletion syndrome", "shortest_name_length": 19}
{"curie": "UMLS:C0854789", "names": ["Resectable Small Bowel Carcinoma", "Resectable Small Intestinal Cancer", "Resectable Carcinoma of Small Bowel", "Small intestine carcinoma resectable", "Resectable Small Intestine Carcinoma", "Small Intestine Carcinoma, Resectable", "Resectable Small Intestinal Carcinoma", "Resectable Carcinoma of Small Intestine", "Resectable Carcinoma of the Small Bowel", "Resectable Carcinoma of the Small Intestine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small intestine carcinoma resectable", "shortest_name_length": 32}
{"curie": "MONDO:0024534", "names": ["DDD", "DDD1", "dark dot disease", "Dowling-Degos Disease", "Dowling-Degos disease", "dowling-degos disease", "DOWLING-DEGOS DISEASE 1", "Dowling-Degos disease 1", "KRT5 Dowling-Degos disease", "Dowling-Degos-Kitamura Disease", "reticular pigment anomaly of flexures", "Reticular pigment anomaly of flexures", "Reticular Pigment Anomaly of Flexures", "RETICULAR PIGMENT ANOMALY OF FLEXURES", "Dowling-Degos disease caused by mutation in KRT5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dowling-Degos disease 1", "shortest_name_length": 3}
{"curie": "MONDO:0015015", "names": ["CBAS6", "congenital bile acid synthesis defect 6", "bile acid synthesis defect, congenital, 6", "BILE ACID SYNTHESIS DEFECT, CONGENITAL, 6", "ACOX2 congenital bile acid synthesis defect", "congenital bile acid synthesis defect type 6", "bile acid synthesis defect, congenital, type 6", "congenital bile acid synthesis defect caused by mutation in ACOX2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital bile acid synthesis defect 6", "shortest_name_length": 5}
{"curie": "MONDO:0003115", "names": ["Airway hemangioma", "Subglottic Angioma", "subglottis angioma", "Subglottis Angioma", "subglottic angioma", "Subglottic Hemangioma", "Angioma of Subglottis", "subglottic hemangioma", "subglottis hemangioma", "Subglottic hemangioma", "angioma of subglottis", "Subglottis Hemangioma", "hemangioma of subglottis", "Hemangioma of Subglottis", "angioma of the subglottis", "Angioma of the Subglottis", "hemangioma of the subglottis", "Hemangioma of the Subglottis", "hemangioma of the Subglottis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subglottic hemangioma", "shortest_name_length": 17}
{"curie": "UMLS:C0279095", "names": ["Adult ALL in Remission", "adult ALL in remission", "ALL in remission, adult", "adult acute lymphoid leukemia in remission", "Adult Acute Lymphoid Leukemia in Remission", "remission, adult acute lymphocytic leukemia", "leukemia in remission, adult acute leukemia", "Adult Acute Lymphocytic Leukemia in Remission", "adult acute lymphocytic leukemia in remission", "Adult Acute Lymphogenous Leukemia in Remission", "lymphocytic leukemia in remission, adult acute", "acute lymphocytic leukemia in remission, adult", "adult acute lymphogenous ;eukemia in remission", "Acute Lymphoblastic Leukemia (ALL) in Remission", "Adult Acute Lymphoblastic Leukemia in Remission", "adult acute lymphoblastic leukemia in remission", "adult precursor lymphoblastic leukemia in remission", "Adult Precursor Lymphoblastic Leukemia in Remission"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Acute Lymphoblastic Leukemia in Remission", "shortest_name_length": 22}
{"curie": "MONDO:0012510", "names": ["COXPD2", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 2", "Combined Oxidative Phosphorylation Deficiency 2", "combined oxidative phosphorylation deficiency 2", "combined oxidative phosphorylation defect type 2", "Combined oxidative phosphorylation defect type 2", "combined oxidative phosphorylation deficiency type 2", "MRPS16 combined oxidative phosphorylation deficiency", "COXPD2 - combined oxidative phosphorylation defect type 2", "Combined oxidative phosphorylation defect type 2 (disorder)", "combined oxidative phosphorylation defect type 2 (diagnosis)", "agenesis of corpus callosum with dysmorphism and fatal lactic acidosis", "CORPUS CALLOSUM, AGENESIS OF, WITH DYSMORPHISM AND FATAL LACTIC ACIDOSIS", "Corpus Callosum, Agenesis Of, With Dysmorphism And Fatal Lactic Acidosis", "corpus callosum, agenesis of, with Dysmorphism and fatal lactic acidosis", "combined oxidative phosphorylation deficiency caused by mutation in MRPS16"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation defect type 2", "shortest_name_length": 6}
{"curie": "MONDO:0015169", "names": ["Maltase-glucoamylase deficiency", "maltase glucoamylase deficiency", "maltase-glucoamylase deficiency", "Maltase glucoamylase deficiency", "chronic diarrhea due to glucoamylase deficiency", "Chronic diarrhea due to glucoamylase deficiency", "Chronic diarrhoea due to glucoamylase deficiency", "Chronic diarrhea due to glucoamylase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic diarrhea due to glucoamylase deficiency", "shortest_name_length": 31}
{"curie": "MONDO:0002189", "names": ["Nodular Hidradenoma", "Nodular hidradenoma", "nodular hidradenoma", "Eccrine nodular hidradenoma", "eccrine nodular hidradenoma", "solid and cystic hidradenoma", "Solid and Cystic Hidradenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nodular hidradenoma", "shortest_name_length": 19}
{"curie": "MONDO:0001067", "names": ["early yaws", "Early yaws", "Mother yaw", "Early Yaws", "yaws early", "yaws; early", "early; yaws", "primary yaws", "Yaws chancre", "yaws primary", "mother; yaws", "yaws; mother", "chancre; yaws", "primary; yaws", "yaws; primary", "chancre of yaws", "Chancre of yaws", "Initial frambesia", "primary frambesia", "Primary frambesia", "Initial framboesia", "Primary framboesia", "Initial yaws lesion", "ulcer; yaws, initial", "yaws; ulcer, initial", "yaws; ulcers, initial", "ulcers; yaws, initial", "yaws; initial lesions", "Early yaws (disorder)", "Primary stage of yaws", "lesion; yaws, initial", "Initial lesion of yaws", "Early yaws (diagnosis)", "initial lesions of yaws", "Initial lesions of yaws", "initial; initial lesions", "primary yaws (diagnosis)", "Initial frambesial ulcer", "initial frambesial ulcer", "yaws bone or joint lesions", "bone and joint yaws lesion", "Bone and joint yaws lesions", "ulcer; yaws, initial, primary", "frambesia, initial or primary", "yaws; initial lesion or ulcer", "bone or joint lesions of yaws", "yaws; ulcer, initial, primary", "Frambesia, initial or primary", "Bone and/or joint yaws lesions", "Bone and joint lesions of yaws", "Initial lesion of yaws (disorder)", "bone and joint lesions due to yaws", "Bone and joint lesions due to yaws", "initial lesions of yaws (diagnosis)", "Initial frambesial ulcer (disorder)", "Initial frambesial ulcer (diagnosis)", "yaws initial lesions frambesial ulcer", "Bone and/or joint yaws lesions (disorder)", "bone or joint lesions of yaws (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early yaws", "shortest_name_length": 10}
{"curie": "UMLS:C0279582", "names": ["L3 Childhood ALL", "L3 pediatric ALL", "Burkitt Leukemia", "L3 Pediatric ALL", "ALL, L3 pediatric", "ALL, pediatric L3", "pediatric ALL, L3", "ALL, childhood L3", "ALL, L3 childhood", "childhood ALL, L3", "Childhood Burkitt Leukemia", "Childhood Burkitt's Leukemia", "pediatric Burkitt's leukemia", "Pediatric Burkitt's Leukemia", "L3 Pediatric Acute Lymphocytic Leukemia", "L3 childhood acute lymphocytic leukemia", "L3 Childhood Acute Lymphocytic Leukemia", "pediatric acute lymphocytic leukemia, L3", "childhood acute lymphocytic leukemia, L3", "L3 acute lymphocytic leukemia, childhood", "acute lymphocytic leukemia, childhood L3", "L3 lymphocytic leukemia, acute childhood", "L3 childhood acute lymphoblastic leukemia", "L3 Childhood Acute Lymphoblastic Leukemia", "L3 Pediatric Acute Lymphoblastic Leukemia", "acute lymphoblastic leukemia, childhood L3", "L3 acute lymphoblastic leukemia, childhood", "L3 lymphoblastic leukemia, acute childhood", "pediatric acute lymphoblastic leukemia, L3", "leukemia, childhood acute lymphocytic , L3", "childhood acute lymphoblastic leukemia, L3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Burkitt Leukemia", "shortest_name_length": 16}
{"curie": "MONDO:0044751", "names": ["chronic diarrhea", "diarrhea chronic", "Chronic diarrhea", "DIARRHEA CHRONIC", "Diarrhea Chronic", "chronic diarrhoea", "chronic; diarrhea", "diarrhea; chronic", "Diarrhea, chronic", "Chronic diarrhoea", "Diarrhoea;chronic", "DIARRHEA, CHRONIC", "diarrhea recurrent", "Recurrent diarrhea", "Diarrhea recurrent", "Diarrhoea recurrent", "Diarrhea, recurrent", "Recurrent diarrhoea", "chronic diarrheal disease", "chronic diarrhea (symptom)", "diarrheal disease, chronic", "Chronic diarrhea (disorder)", "diarrhea recurrent (symptom)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic diarrheal disease", "shortest_name_length": 16}
{"curie": "UMLS:C4330843", "names": ["Nutritional Calciopenic Rickets", "Nutritional Calcium Deficient Rickets"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nutritional Calcium Deficient Rickets", "shortest_name_length": 31}
{"curie": "MONDO:0018419", "names": ["SPG67", "autosomal recessive spastic paraplegia type 67", "Autosomal recessive spastic paraplegia type 67", "familial spastic paraplegia autosomal recessive type 67", "Autosomal recessive spastic paraplegia type 67 (disorder)", "Autosomal recessive spastic paraplegia type 67 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive spastic paraplegia type 67", "shortest_name_length": 5}
{"curie": "MONDO:0001375", "names": ["bladder trigone cancer", "trigone of urinary bladder cancer", "cancer of trigone of urinary bladder", "Malignant tumor of trigone of bladder", "malignant tumor of trigone of bladder", "Malignant tumour of trigone of bladder", "malignant neoplasm of trigone of bladder", "Malignant neoplasm of trigone of bladder", "malignant tumor of trigone of urinary bladder", "Malignant tumor of trigone of urinary bladder", "malignant trigone of urinary bladder neoplasm", "Malignant tumour of trigone of urinary bladder", "Malignant neoplasm of trigone of urinary bladder", "malignant neoplasm of trigone of urinary bladder", "malignant neoplasm of trigone of bladder (diagnosis)", "Malignant tumor of trigone of urinary bladder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder trigone cancer", "shortest_name_length": 22}
{"curie": "UMLS:C1518707", "names": ["Ovarian Dermoid Cyst with Secondary Pituitary-Type Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Dermoid Cyst with Secondary Pituitary-Type Tumor", "shortest_name_length": 56}
{"curie": "MONDO:0020293", "names": ["ascending aorta anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ascending aorta anomaly", "shortest_name_length": 23}
{"curie": "MONDO:0007849", "names": ["KEFH", "keratitis fugax hereditaria", "KERATITIS FUGAX HEREDITARIA", "Keratitis Fugax Hereditaria", "keratoendothelitis fugax hereditaria", "Keratoendotheliitis fugax hereditaria", "KERATOENDOTHELIITIS fugax hereditaria", "KERATOENDOTHELIITIS FUGAX HEREDITARIA", "Keratoendotheliitis Fugax Hereditaria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratitis fugax hereditaria", "shortest_name_length": 4}
{"curie": "UMLS:C0009045", "names": ["Malar and maxillary bones, closed fracture", "Closed Fracture of Malar and Maxillary Bone", "Closed fracture of malar and maxillary bones", "Closed fracture of malar AND/OR maxillary bones", "closed fracture of malar and/or maxillary bones", "Closed fracture of malar and maxillary bones, NOS", "Closed fracture of malar AND/OR maxillary bones (disorder)", "closed fracture of malar and/or maxillary bones (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Closed fracture of malar AND/OR maxillary bones", "shortest_name_length": 42}
{"curie": "UMLS:C0856875", "names": ["Diabetic ketoacidotic hyperglycemic coma", "Diabetic ketoacidotic hyperglycaemic coma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diabetic ketoacidotic hyperglycemic coma", "shortest_name_length": 40}
{"curie": "MONDO:0027353", "names": ["DKCB4", "autosomal recessive dyskeratosis congenita 4", "dyskeratosis congenita, autosomal recessive 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive dyskeratosis congenita 4", "shortest_name_length": 5}
{"curie": "UMLS:C1333023", "names": ["Chondrosarcoma NCI Grade 3", "Chondrosarcoma NCI Grade III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chondrosarcoma NCI Grade 3", "shortest_name_length": 26}
{"curie": "UMLS:C1879667", "names": ["Aflatoxins Toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aflatoxins Toxicity", "shortest_name_length": 19}
{"curie": "UMLS:C1335116", "names": ["Mouth Adenoma", "Adenoma of Mouth", "Oral Cavity Adenoma", "Adenoma of the Mouth", "Adenoma of Oral Cavity", "Adenoma of the Oral Cavity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral Cavity Adenoma", "shortest_name_length": 13}
{"curie": "MONDO:0030730", "names": ["TEVANED2", "TEBIVANED2", "Tessadori-van Haaften neurodevelopmental syndrome 2", "TESSADORI-BICKNELL-VAN HAAFTEN NEURODEVELOPMENTAL SYNDROME 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tessadori-van Haaften neurodevelopmental syndrome 2", "shortest_name_length": 8}
{"curie": "UMLS:C0085094", "names": ["close head injury", "Closed Head Injury", "Closed head injury", "closed head injury", "Injury;closed head", "closed head trauma", "Closed Head Trauma", "HEAD INJURY CLOSED", "Head Trauma, Closed", "Head Injury, Closed", "Closed Head Traumas", "close head injuries", "Closed head injuries", "Closed Head Injuries", "closed head injuries", "Head Traumas, Closed", "Closed injury of head", "Head Injuries, Closed", "Injuries, Closed Head", "Nonpenetrating Head Injury", "Head Injury, Nonpenetrating", "Nonpenetrating Head Injuries", "Head Injuries, Nonpenetrating", "Closed injury of head (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Closed head injuries", "shortest_name_length": 17}
{"curie": "UMLS:C5418883", "names": ["Metastatic Malignant Mixed Mesodermal (Mullerian) Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Malignant Mixed Mesodermal (Mullerian) Tumor", "shortest_name_length": 55}
{"curie": "MONDO:0002464", "names": ["lacrimal gland tumor", "lacrimal gland cancer", "gland lacrimal tumors", "gland lacrimal tumours", "Lacrimal gland neoplasm", "Tumor of lacrimal gland", "Lacrimal Gland Neoplasm", "cancer of lacrimal gland", "Tumour of lacrimal gland", "Neoplasm of lacrimal gland", "Neoplasm of Lacrimal Gland", "neoplasm of lacrimal gland", "tumor of the lacrimal gland", "Malignant Lacrimal Gland Tumor", "Neoplasm of the Lacrimal Gland", "malignant lacrimal gland tumor", "Malignant tumor of lacrimal gland", "malignant tumor of lacrimal gland", "Malignant Lacrimal Gland Neoplasm", "malignant lacrimal gland neoplasm", "Malignant Tumor of Lacrimal Gland", "malignant tumour of lacrimal gland", "Malignant tumour of lacrimal gland", "eye neoplasm lacrimal system gland", "Malignant Neoplasm of Lacrimal Gland", "Malignant neoplasm of lacrimal gland", "malignant neoplasm of lacrimal gland", "malignant tumor of the lacrimal gland", "Neoplasm of lacrimal gland (disorder)", "Malignant Tumor of the Lacrimal Gland", "Neoplasm of lacrimal gland (diagnosis)", "Malignant Neoplasm of the Lacrimal Gland", "malignant neoplasm of the lacrimal gland", "Malignant tumor of lacrimal gland (disorder)", "malignant neoplasm of lacrimal gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lacrimal gland cancer", "shortest_name_length": 20}
{"curie": "UMLS:C3897085", "names": ["Stage IIC Colon Cancer", "Stage IIC Colon Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIC Colon Cancer AJCC v7", "shortest_name_length": 22}
{"curie": "UMLS:C0333494", "names": ["venofibrosis", "Venofibrosis", "venosclerosis", "Venosclerosis", "Phleboscleroses", "phlebosclerosis", "Phlebosclerosis", "Venofibrosis, NOS", "Venosclerosis, NOS", "Phlebosclerosis, NOS", "venofibrosis (diagnosis)", "Phlebosclerosis (disorder)", "phlebosclerosis (diagnosis)", "Phlebosclerosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Phlebosclerosis", "shortest_name_length": 12}
{"curie": "MONDO:0016937", "names": ["Duplication of chromosome 19", "partial trisomy of chromosome 19", "Partial trisomy of chromosome 19", "Partial duplication of chromosome 19", "partial duplication of chromosome 19", "partial duplication of chromosome type 19", "Partial trisomy of chromosome 19 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of chromosome 19", "shortest_name_length": 28}
{"curie": "UMLS:C4329301", "names": ["Anastomosing Hemangioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anastomosing Hemangioma", "shortest_name_length": 23}
{"curie": "UMLS:C1336189", "names": ["Stage IIB Nasopharyngeal Keratinizing Squamous Cell Carcinoma", "Nasopharyngeal Keratinizing Squamous Cell Carcinoma Stage IIB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Nasopharyngeal Keratinizing Squamous Cell Carcinoma", "shortest_name_length": 61}
{"curie": "UMLS:C0857331", "names": ["Acute liver damage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute liver damage", "shortest_name_length": 18}
{"curie": "MONDO:0013077", "names": ["Santos syndrome", "SANTOS SYNDROME", "Santos Syndrome", "FIBULAR AGENESIS/HYPOPLASIA, OLIGODACTYLOUS CLUBFEET, AND ANONYCHIA/NAIL HYPOPLASIA SYNDROME", "fibular agenesis/hypoplasia, oligodactylous clubfeet, and anonychia/nail hypoplasia syndrome", "Fibular Agenesis-Hypoplasia, Oligodactylous Clubfeet, and Anonychia-Nail Hypoplasia Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Santos syndrome", "shortest_name_length": 15}
{"curie": "UMLS:C0856901", "names": ["Retinol Deficiency", "Retinol deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retinol Deficiency", "shortest_name_length": 18}
{"curie": "EFO:0005129", "names": ["hepatitis C induced liver cirrhosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatitis C induced liver cirrhosis", "shortest_name_length": 35}
{"curie": "MONDO:0043143", "names": ["Thomas Jewett Raines syndrome", "Thomas-Jewett-Raines syndrome", "microphthalmia-microtia-fetal akinesia", "microphthalmia microtia fetal akinesia", "Microphthalmia-microtia-fetal akinesia syndrome", "Microphthalmia, microtia, fetal akinesia syndrome", "Microphthalmia, microtia, foetal akinesia syndrome", "Microphthalmia, microtia, fetal akinesia syndrome (disorder)", "fetal akinesia with characteristic facial appearance, severe microphthalmia, microtia, and truncus arteriosus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microphthalmia microtia fetal akinesia", "shortest_name_length": 29}
{"curie": "MONDO:0016027", "names": ["BFNS", "Benign Neonatal Epilepsy", "Benign neonatal epilepsy", "Benign neonatal seizures", "benign neonatal seizures", "Neonatal Epilepsy, Benign", "Epilepsy, Benign Neonatal", "benign familial convulsion", "Benign Neonatal Epilepsies", "Benign Familial Convulsion", "Benign Neonatal Convulsion", "Convulsion, Benign Neonatal", "benign familial convulsions", "Neonatal Convulsion, Benign", "benign neonatal convulsions", "Benign Neonatal Convulsions", "Epilepsies, Benign Neonatal", "Benign Familial Convulsions", "Benign neonatal convulsions", "Neonatal Epilepsies, Benign", "Convulsions, Benign Neonatal", "Neonatal Convulsions, Benign", "Benign Familal Neonatal Seizures", "benign familal neonatal seizures", "Benign Familial Neonatal Seizures", "benign familial neonatal seizures", "Benign Neonatal-Infantile Epilepsy", "seizures, benign familial neonatal", "Neonatal-Infantile Epilepsy, Benign", "Epilepsy, Benign Neonatal-Infantile", "Epilepsy, Benign Neonatal Infantile", "benign familial neonatal convulsions", "Benign Neonatal-Infantile Epilepsies", "Neonatal-Infantile Epilepsies, Benign", "Epilepsies, Benign Neonatal-Infantile", "Benign neonatal convulsions (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neonatal seizures", "shortest_name_length": 4}
{"curie": "MONDO:0024309", "names": ["HSN2A", "HSN 2A", "HSAN2A", "HSN IIA", "HSAN 2A", "HSAN IIA", "Morvan disease", "ACROOSTEOLYSIS, NEUROGENIC", "acroosteolysis, neurogenic", "acroosteolysis, Giaccai type", "ACROOSTEOLYSIS, GIACCAI TYPE", "neuropathy, congenital sensory", "NEUROPATHY, CONGENITAL SENSORY", "neuropathy, hereditary sensory, type 2A", "Neuropathy, Hereditary Sensory, Type IIA", "NEUROPATHY, HEREDITARY SENSORY, TYPE IIA", "NEUROPATHY, PROGRESSIVE SENSORY, OF CHILDREN", "neuropathy, progressive sensory, of children", "Hereditary sensory autonomic neuropathy type IIA", "hereditary sensory and autonomic neuropathy type 2A", "hereditary sensory and autonomic neuropathy type IIA", "neuropathy, hereditary sensory and autonomic, type 2A", "neuropathy, hereditary sensory and autonomic, type II", "neuropathy, hereditary sensory and autonomic, type IIA", "NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA", "Neuropathy, Hereditary Sensory And Autonomic, Type IIA", "Hereditary sensory autonomic neuropathy type IIA (disorder)", "NEUROPATHY, HEREDITARY SENSORY RADICULAR, AUTOSOMAL RECESSIVE", "neuropathy, hereditary sensory radicular, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuropathy, hereditary sensory and autonomic, type 2A", "shortest_name_length": 5}
{"curie": "MONDO:0007239", "names": ["EI", "BIE", "EHK", "BCIE", "Bullous ichthyosis", "bullous ichthyosis", "epidermolytic ichthyosis", "Epidermolytic ichthyosis", "EPIDERMOLYTIC ICHTHYOSIS", "Epidermolytic Ichthyosis", "Epidermolytic Hyperkeratoses", "epidermolytic hyperkeratosis", "Epidermolytic Hyperkeratosis", "Epidermolytic hyperkeratosis", "Dominant ichthyosis vulgaris", "EPIDERMOLYTIC HYPERKERATOSIS", "Hyperkeratosis, Epidermolytic", "ichthyosis hystrix Brocq type", "Ichthyosis hystrix Brocq type", "Hyperkeratoses, Epidermolytic", "Hyperkeratosis, epidermolytic", "epidermolytic hyperkeratosis 1", "Bullous ichthyosiform erythroderma", "bullous ichthyosiform erythroderma", "BULLOUS ICHTHYOSIFORM ERYTHRODERMA", "Bullous Ichthyosiform Erythroderma", "Erythroderma, Bullous Ichthyosiform", "Bullous Ichthyosiform Erythrodermas", "Ichthyosiform Erythroderma, Bullous", "Bullous Erythroderma Ichthyosiforme", "Erythroderma Ichthyosiforme, Bullous", "Ichthyosiforme, Bullous Erythroderma", "Ichthyosiform Erythrodermas, Bullous", "Bullous Erythroderma Ichthyosiformes", "Erythrodermas, Bullous Ichthyosiform", "Ichthyosiformes, Bullous Erythroderma", "Erythroderma Ichthyosiformes, Bullous", "epidermolytic hyperkeratosis, late-onset", "Epidermolytic Hyperkeratosis, Late-Onset", "BIE - Bullous ichthyosiform erythroderma", "EPIDERMOLYTIC HYPERKERATOSIS, LATE-ONSET", "Epidermolytic palmoplantar hyperkeratosis", "epidermolytic palmoplantar hyperkeratosis", "Autosomal dominant epidermolytic ichthyosis", "autosomal dominant epidermolytic ichthyosis", "bullous ichthyosiform erythroderma congenita", "ichthyosiforme congenitum bullosum; erythema", "erythema; ichthyosiforme congenitum bullosum", "bullous congenital ichthyosiform erythroderma", "Bullous Ichthyosiform Erythroderma Congenital", "Bullous congenital ichthyosiform erythroderma", "congenital bullous ichthyosiform erythroderma", "BULLOUS CONGENITAL ICHTHYOSIFORM ERYTHRODERMA", "Bullous ichthyosiform erythroderma (disorder)", "Congenital bullous ichthyosiform erythroderma", "Congenital Bullous Ichthyosiform Erythroderma", "Bullous Congenital Ichthyosiform Erythroderma", "Congenital ichthyosiform erythroderma, bullous", "Ichthyosiform Erythroderma, Bullous Congenital", "Congenital Ichthyosiform Erythroderma, Bullous", "Epidermolytic palmoplantar keratoderma of Vorner", "Bullous congenital ichthyosiform erythroderma of Brock", "bullous congenital ichthyosiform erythroderma of Brock", "Bullous Erythroderma Ichthyosiformis Congenita of Brocq", "BULLOUS ERYTHRODERMA ICHTHYOSIFORMIS CONGENITA OF BROCQ", "bullous erythroderma Ichthyosiformis congenita of Brocq", "congenital bullous ichthyosiform erythroderma (diagnosis)", "Epidermolytic palmoplantar keratoderma of Vorner (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolytic ichthyosis", "shortest_name_length": 2}
{"curie": "MONDO:0024934", "names": ["Fish Disease", "fish disease", "Fish Diseases", "fish diseases", "Disease, Fish", "disease, fish", "diseases, fish", "Diseases, Fish", "Fishes--Diseases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fish disease", "shortest_name_length": 12}
{"curie": "MONDO:0044807", "names": ["Familial Dystonia", "familial dystonia", "Familial Dystonias", "inherited dystonia", "Dystonia, Familial", "Hereditary Dystonia", "Dystonias, Familial", "Hereditary Dystonias", "Dystonia, Hereditary", "rare genetic dystonia", "Dystonias, Hereditary", "hereditary dystonic disorder", "rare genetic dystonic disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited dystonia", "shortest_name_length": 17}
{"curie": "UMLS:C1513041", "names": ["Measurable Disease", "measurable disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Measurable Disease", "shortest_name_length": 18}
{"curie": "UMLS:C4525106", "names": ["Rectal Cancer by AJCC v8 Stage", "Rectal Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rectal Cancer by AJCC v8 Stage", "shortest_name_length": 30}
{"curie": "MONDO:0018447", "names": ["chondromyxoid fibroma", "Chondromyxoid Fibroma", "Chondromyxoid fibroma", "FIBROMA, CHONDROMYXOID", "CMF - Chondromyxoid fibroma", "Chondromyxoid fibroma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chondromyxoid fibroma", "shortest_name_length": 21}
{"curie": "MONDO:0000831", "names": ["thrombus", "Thromboses", "thrombosis", "blood clot", "Thrombosed", "THROMBOSIS", "Thrombosis", "clot, blood", "blood Clots", "Clots, blood", "Thrombosis NOS", "Thrombosis, NOS", "thrombotic disease", "Thrombotic disorder", "thrombotic disorder", "Thrombosis (disorder)", "Thrombosis (qualifier value)", "Thrombotic disorder (navigational concept)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombotic disease", "shortest_name_length": 8}
{"curie": "MONDO:0021207", "names": ["Crohn jejunitis", "Crohn's jejunitis", "Crohn disease of jejunum", "Crohn's disease of jejunum", "Crohn's disease of jejunum (disorder)", "Crohn's disease of jejunum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Crohn jejunitis", "shortest_name_length": 15}
{"curie": "UMLS:C0028259", "names": ["Nodule", "NODULE", "nodule", "Nodules", "nodules", "Nodule, NOS", "Nodule (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nodule", "shortest_name_length": 6}
{"curie": "MONDO:0001655", "names": ["dissociated nystagmus", "Dissociated nystagmus", "nystagmus dissociated", "Dissociated Nystagmus", "Nystagmus, Dissociated", "Dissociated nystagmus (disorder)", "dissociated nystagmus (diagnosis)", "dissociated nystagmus (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dissociated nystagmus", "shortest_name_length": 21}
{"curie": "MONDO:0010320", "names": ["RP23", "RP 23", "RETINITIS PIGMENTOSA 23", "retinitis pigmentosa 23", "OFD1 retinitis pigmentosa", "retinitis pigmentosa type 23", "retinitis pigmentosa 23, X-linked recessive", "retinitis pigmentosa caused by mutation in OFD1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 23", "shortest_name_length": 4}
{"curie": "UMLS:C2362914", "names": ["clinical depression", "Clinical depression", "depression clinical", "clinical depressions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical depression", "shortest_name_length": 19}
{"curie": "UMLS:C4528551", "names": ["Stage I Breast Cancer", "Anatomic Stage I Breast Cancer AJCC v8", "Anatomic Stage I Breast Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anatomic Stage I Breast Cancer AJCC v8", "shortest_name_length": 21}
{"curie": "MONDO:0013384", "names": ["HSCR4", "EDN3 Hirschsprung disease", "susceptibility to Hirschsprung disease 4", "Hirschsprung disease, susceptibility to, 4", "HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 4", "Hirschsprung disease, susceptibility to, type 4", "Hirschsprung disease caused by mutation in EDN3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hirschsprung disease, susceptibility to, 4", "shortest_name_length": 5}
{"curie": "MONDO:0008593", "names": ["TCMGLY", "Trichomegaly", "TRICHOMEGALY", "trichomegaly", "eyelashes, long", "EYELASHES, LONG"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichomegaly", "shortest_name_length": 6}
{"curie": "MONDO:0700173", "names": ["Horse Sarcoid", "horse sarcoid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "horse sarcoid", "shortest_name_length": 13}
{"curie": "UMLS:C4763841", "names": ["Metastatic Giant Cell Urothelial Carcinoma", "Metastatic Giant Cell Bladder Urothelial Carcinoma", "Metastatic Giant Cell  Bladder Urothelial Carcinoma", "Metastatic Giant Cell Urothelial Carcinoma of the Bladder", "Metastatic Infiltrating Bladder Urothelial Carcinoma with Giant Cells"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Infiltrating Bladder Urothelial Carcinoma with Giant Cells", "shortest_name_length": 42}
{"curie": "MONDO:0006324", "names": ["Normal Breast-Like Subtype of Breast Cancer", "normal breast-like subtype of breast cancer", "normal breast-like subtype of breast carcinoma", "Normal Breast-Like Subtype of Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "normal breast-like subtype of breast carcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0100015", "names": ["DYT-GNAL", "adult-onset segmental dystonia", "an adult-onset, focal or segmental, isolated dystonia that is characterized by cervical or cranial dystonia that often begins in the fourth decade (range 7-54 years)."], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult-onset segmental dystonia", "shortest_name_length": 8}
{"curie": "MONDO:0015863", "names": ["polyembryoma", "Polyembryoma", "gonadal polyembryoma", "Gonadal Polyembryoma", "Polyembryoma (disorder)", "polyembryoma (diagnosis)", "Polyembryoma (morphologic abnormality)", "Embryonal carcinoma, polyembryonal type", "Embryonal carcinoma - polyembryonal type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyembryoma", "shortest_name_length": 12}
{"curie": "MONDO:0800119", "names": ["PIBO", "postinfectious bronchiolitis obliterans"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postinfectious bronchiolitis obliterans", "shortest_name_length": 4}
{"curie": "MONDO:0003238", "names": ["cervical adenomyoma", "Cervical Adenomyoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical adenomyoma", "shortest_name_length": 19}
{"curie": "UMLS:C0473771", "names": ["Secondary generalised osteoporosis", "Secondary generalized osteoporosis", "osteoporosis secondary generalized", "Secondary generalized osteoporosis (disorder)", "Secondary generalized osteoporosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary generalized osteoporosis", "shortest_name_length": 34}
{"curie": "UMLS:C3272613", "names": ["Colorectal Enterochromaffin Cell Serotonin-Producing Neuroendocrine Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Enterochromaffin Cell Serotonin-Producing Neuroendocrine Tumor", "shortest_name_length": 73}
{"curie": "MONDO:0007051", "names": ["AFA SYNDROME", "AFA syndrome", "Hughes syndrome", "hughes syndrome", "thick lips and oral mucosa", "Thick lips and oral mucosa", "THICK LIPS AND ORAL MUCOSA", "ACROMEGALOID FACIAL APPEARANCE SYNDROME", "acromegaloid facial appearance syndrome", "Acromegaloid facial appearance syndrome", "acromegaloid facial appearance (AFA) syndrome", "Acromegaloid facial appearance syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acromegaloid facial appearance syndrome", "shortest_name_length": 12}
{"curie": "UMLS:C4288093", "names": ["Tubal Hyperplasia", "Tubal Epithelial Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tubal Hyperplasia", "shortest_name_length": 17}
{"curie": "MONDO:0030298", "names": ["HAE8", "ANGIOEDEMA, HEREDITARY, 8", "angioedema, hereditary, 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angioedema, hereditary, 8", "shortest_name_length": 4}
{"curie": "MONDO:0001042", "names": ["patella tendinitis", "tendinitis; patella", "Patellar tendinitis", "patella; tendinitis", "patellar tendonitis", "patellar tendinitis", "Patellar tendonitis", "tendinitis of patella", "Patellar ligament desmitis", "Patellar tendonitis (disorder)", "patellar tendinitis (diagnosis)", "Patellar tendinitis, unspecified knee"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "patellar tendinitis", "shortest_name_length": 18}
{"curie": "UMLS:C1709484", "names": ["Patient Chemical Contamination Due To Medical Device Failure Or Malfunction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Patient Chemical Contamination Due To Medical Device Failure Or Malfunction", "shortest_name_length": 75}
{"curie": "UMLS:C4330658", "names": ["Salivary Gland MASC", "Salivary Gland Secretory Carcinoma", "Mammary Analogue Secretory Carcinoma of Salivary Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Salivary Gland Secretory Carcinoma", "shortest_name_length": 19}
{"curie": "UMLS:C5206778", "names": ["Recurrent Rhabdoid Tumor of the Kidney"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Rhabdoid Tumor of the Kidney", "shortest_name_length": 38}
{"curie": "UMLS:C1266096", "names": ["Malignant Type B2 Thymoma", "Thymoma, type B2, malignant", "Thymoma, cortical, malignant", "Thymoma, type B2, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thymoma, type B2, malignant", "shortest_name_length": 25}
{"curie": "MONDO:0009886", "names": ["PLEOCONIAL MYOPATHY WITH SALT CRAVING", "pleoconial myopathy with salt craving", "Pleoconial Myopathy with Salt Craving"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pleoconial myopathy with salt craving", "shortest_name_length": 37}
{"curie": "UMLS:C5236957", "names": ["Unresectable Liver and Intrahepatic Bile Duct Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Liver and Intrahepatic Bile Duct Carcinoma", "shortest_name_length": 55}
{"curie": "UMLS:C5206861", "names": ["ICANS", "cell-associated neurotoxicity", "Immune Effector Cell Encephalopathy", "IEC-associated Neurotoxicity Syndrome", "Immune Effector Cell Associated Neurotoxicity Syndrome", "immune effector cell-associated neurotoxicity syndrome", "Immune effector cell-associated neurotoxicity syndrome", "ICANS - immune effector cell-associated neurotoxicity syndrome", "Immune effector cell-associated neurotoxicity syndrome (disorder)", "immune effector cell-associated neurotoxicity syndrome (diagnosis)", "toxic encephalopathy immune effector cell-associated neurotoxicity syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cell-associated neurotoxicity", "shortest_name_length": 5}
{"curie": "UMLS:C1405308", "names": ["VAPP", "OPV associated Paralytic Poliomyelitis", "Vaccine-Associated Paralytic Poliomyelitis", "vaccine-associated paralytic poliomyelitis", "poliomyelitis paralytic vaccine-associated", "Vaccine associated paralytic poliomyelitis", "poliomyelitis; paralytic, vaccine-associated", "vaccine-associated paralytic poliomyelitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaccine associated paralytic poliomyelitis", "shortest_name_length": 4}
{"curie": "MONDO:0015267", "names": ["FS", "MMT", "FGLDS", "ODED syndrome", "MODED syndrome", "Feingold Syndrome", "Feingold syndrome", "Brunner-Winter syndrome", "oculo-digito-esophageal-duodenal syndrome", "microcephaly-oculo-digito-esophageal-duodenal syndrome", "microcephaly-digital anomalies-normal intelligence syndrome", "microcephaly-oculo-digito-esophageal-duodenal syndrome syndrome", "microcephaly-intellectual disability-tracheoesophageal fistula syndrome", "digital anomalies with short palpebral fissures and atresia of esophagus or duodenum", "digital anomalies with short palpebral fissures and atresia of esophagus, or duodenum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Feingold syndrome", "shortest_name_length": 2}
{"curie": "UMLS:C3272433", "names": ["Noninvasive Papillary Neoplasm, Pancreatobiliary Type", "Ampullary Noninvasive Papillary Neoplasm, Pancreatobiliary Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ampullary Noninvasive Papillary Neoplasm, Pancreatobiliary Type", "shortest_name_length": 53}
{"curie": "UMLS:C0684963", "names": ["Metastases to pharynx", "Metastasis to the Pharynx", "Metastatic Tumor to the Pharynx", "Metastatic Neoplasm to the Pharynx", "Secondary malignant neoplasm of pharynx", "pharyngeal neoplasm malignant secondary", "Metastatic malignant neoplasm of pharynx", "Metastatic malignant neoplasm to pharynx", "Metastatic Malignant Neoplasm to the Pharynx", "Secondary malignant neoplasm of pharynx, NOS", "Metastatic Malignant Neoplasm in the Pharynx", "Metastatic malignant neoplasm to pharynx, NOS", "Metastatic malignant neoplasm to pharynx (disorder)", "Secondary malignant neoplasm of pharynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to pharynx", "shortest_name_length": 21}
{"curie": "UMLS:C1332975", "names": ["Childhood Intracranial Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Intracranial Neoplasm", "shortest_name_length": 31}
{"curie": "UMLS:C0751072", "names": ["FTLD", "FTLDs", "Frontotemporal Lobar Degeneration", "Frontotemporal Lobar Degenerations", "Lobar Degeneration, Frontotemporal", "Degeneration, Frontotemporal Lobar", "Lobar Degenerations, Frontotemporal", "Degenerations, Frontotemporal Lobar"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Frontotemporal Lobar Degeneration", "shortest_name_length": 4}
{"curie": "MONDO:0000836", "names": ["bone structure disease", "disease of bone structure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disease of bone structure", "shortest_name_length": 22}
{"curie": "MONDO:0014206", "names": ["ILLD", "ILFS2, FORMERLY", "PAP, Reunion island type", "infantile liver failure syndrome 2", "INTERSTITIAL LUNG AND LIVER DISEASE", "interstitial lung and liver disease", "Interstitial lung and liver disease", "INFANTILE LIVER FAILURE SYNDROME 2, FORMERLY", "infantile liver failure syndrome 2, formerly", "pulmonary alveolar proteinosis, Reunion Island", "PULMONARY ALVEOLAR PROTEINOSIS, REUNION ISLAND", "Pulmonary alveolar proteinosis Reunion island type", "Pulmonary alveolar proteinosis, Reunion island type", "pulmonary alveolar proteinosis, Reunion island type", "Hereditary pulmonary alveolar proteinosis with hepatic involvement", "hereditary pulmonary alveolar proteinosis with hepatic involvement", "Severe early-onset pulmonary alveolar proteinosis due to MARS deficiency", "severe early-onset pulmonary alveolar proteinosis due to MARS deficiency", "Severe early-onset pulmonary alveolar proteinosis due to methionyl-transfer ribonucleic acid synthetase 1 deficiency", "Severe early-onset pulmonary alveolar proteinosis due to methionyl-transfer ribonucleic acid synthetase 1 deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe early-onset pulmonary alveolar proteinosis due to MARS deficiency", "shortest_name_length": 4}
{"curie": "UMLS:C4525740", "names": ["Stage IIIB Colorectal Neuroendocrine Tumor", "Stage IIIB Colorectal Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Colorectal Neuroendocrine Tumor AJCC v8", "shortest_name_length": 42}
{"curie": "MONDO:0009833", "names": ["SDS", "Shwachman syndrome", "shwachman syndrome", "Shwachman Syndrome", "shwachman's syndrome", "Shwachman's syndrome", "schwachman's syndrome", "Schwachman's syndrome", "Shwachman Bodian Syndrome", "Shwachman-Bodian syndrome", "SHWACHMAN-BODIAN SYNDROME", "Shwachman-Bodian Syndrome", "shwachman-diamond syndrome", "Shwachman-Diamond syndrome", "shwachman diamond syndrome", "Shwachman-Diamond Syndrome", "Shwachman Diamond Syndrome", "SHWACHMAN-DIAMOND SYNDROME", "Schwachman-Bodian syndrome", "schwachman-diamond syndrome", "Schwachman-Diamond syndrome", "schwachman diamond syndrome", "schwachmann diamond syndrome", "Schwachmann-Diamond syndrome", "schwachmann-diamond syndrome", "Shwachman syndrome (disorder)", "[OBSOLETE] Shwachman syndrome", "Pancreas Congenital Lipomatoses", "Pancreas Congenital Lipomatosis", "Shwachman-Diamond-Oski Syndrome", "congenital lipomatosis pancreas", "Shwachman Diamond Oski Syndrome", "Shwachman's syndrome (diagnosis)", "Shwachman Bodian Diamond Syndrome", "Shwachman-Bodian-Diamond Syndrome", "Shwachman-Bodian-Diamond syndrome", "congenital lipomatosis of pancreas", "Congenital lipomatosis of pancreas", "Congenital Lipomatosis of Pancreas", "LIPOMATOSIS OF PANCREAS, CONGENITAL", "lipomatosis of pancreas, congenital", "Shwachman-Diamond type metaphyseal dysplasia", "Metaphyseal chondrodysplasia, Shwachman type", "Metaphyseal Chondrodysplasia, Shwachman Type", "Pancreatic insufficiency and bone marrow dysfunction", "Pancreatic Insufficiency and Bone Marrow Dysfunction", "pancreatic insufficiency and bone marrow dysfunction", "PANCREATIC INSUFFICIENCY AND BONE MARROW DYSFUNCTION", "Metaphyseal dysplasia with malabsorption and neutropenia", "Metaphyseal chondrodysplasia with pancreatic insufficiency AND neutropenia", "Metaphyseal chondrodysplasia with pancreatic insufficiency and neutropenia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Shwachman-Diamond syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0019120", "names": ["pili bifurcati", "Pili bifurcati", "Pili bifurcati (disorder)", "pili bifurcati (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pili bifurcati", "shortest_name_length": 14}
{"curie": "MONDO:0002696", "names": ["adenoma of testis", "Sertoli cell tumor", "Sertoli Cell Tumor", "testicular adenoma", "sertoli cell tumor", "Testicular adenoma", "Sertoli cell tumour", "Tumor, Sertoli Cell", "cell sertoli tumors", "sertoli cell tumour", "Sertoli cell adenoma", "Pick tubular adenoma", "Tubular androblastoma", "tubular androblastoma", "Sertoli cell neoplasm", "Sertoli cell adenomas", "Sertoli cell tumor NOS", "Pick's tubular adenoma", "Sertoli cell neoplasia", "Sertoli cell tumor, NOS", "Sertoli cell tumour NOS", "Sertoli cell tumour, NOS", "Sustentacular cell tumor", "Sustentacular cell tumour", "Tubular androblastoma, NOS", "adenoma of testis (diagnosis)", "Sertoli cell tumor (morphologic abnormality)", "tubular androblastoma NOS (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sertoli cell tumor", "shortest_name_length": 17}
{"curie": "UMLS:C5556767", "names": ["Recurrent Clear Cell Sarcoma of Soft Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Clear Cell Sarcoma of Soft Tissue", "shortest_name_length": 43}
{"curie": "UMLS:C3273093", "names": ["Gallbladder ICPN with Low Grade Intraepithelial Neoplasia", "Gallbladder Intracholecystic Papillary Neoplasm, Low Grade", "Gallbladder Intracholecystic Papillary Neoplasm, Low-Grade", "Gallbladder Papillary Neoplasm with Low Grade Intraepithelial Neoplasia", "Intracystic papillary neoplasm with low grade intraepithelial neoplasia", "Intracystic Papillary Neoplasm with Low Grade Intraepithelial Neoplasia", "Gallbladder Intracholecystic Papillary Neoplasm with Low Grade Intraepithelial Neoplasia", "Gallbladder Intracystic/Intaductal Papillary Neoplasm with Low Grade Intraepithelial Neoplasia", "Intracystic papillary neoplasm with low grade intraepithelial neoplasia (morphologic abnormality)", "Gallbladder Intracholecystic Papillary (Tubular) Neoplasm with Low Grade Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intracystic papillary neoplasm with low grade intraepithelial neoplasia", "shortest_name_length": 57}
{"curie": "UMLS:C5555175", "names": ["Refractory Fallopian Tube Endometrioid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Fallopian Tube Endometrioid Adenocarcinoma", "shortest_name_length": 53}
{"curie": "MONDO:0015827", "names": ["WD", "FR", "dRTA", "DRTA1", "DRTA4", "AD dRTA", "distal RTA", "type I RTA", "Classic RTA", "classic RTA", "BAND 3 MEMPHIS", "Classic Type RTA", "RTA, Classic Type", "Classic Type RTAs", "RTA, CLASSIC TYPE", "Gradient Type RTA", "RTA, Gradient Type", "RTAs, Classic Type", "Gradient Type RTAs", "RTA, GRADIENT TYPE", "RTAs, Gradient Type", "BLOOD GROUP--FROESE", "Type 1 (distal) RTA", "RENAL TUBULAR ACIDOSIS I", "BAND 3 MEMPHIS PHENOTYPE", "Renal Tubular Acidosis I", "Renal Tubular Acidosis 1", "BLOOD GROUP--WALDNER TYPE", "DIEGO BLOOD GROUP ANTIGEN", "SWANN BLOOD GROUP ANTIGEN", "FROESE BLOOD GROUP ANTIGEN", "ACANTHOCYTOSIS, ONE FORM OF", "WALDNER BLOOD GROUP ANTIGEN", "Distal Renal Tubular Acidosis", "Type I Renal Tubular Acidosis", "distal renal tubular acidosis", "Distal renal tubular acidosis", "renal tubular acidosis type 1", "renal tubular acidosis distal", "acidosis distal renal tubular", "Type I renal tubular acidosis", "renal tubular acidosis type i", "Renal tubular acidosis type 1", "RENAL TUBULAR ACIDOSIS DISTAL", "Renal tubular acidosis, type I", "renal tubular acidosis, distal", "Renal tubular acidosis, type 1", "Renal Tubular Acidosis, Type I", "Renal tubular acidosis, distal", "ACANTHOCYTOSIS DUE TO BAND 3 HT", "Acidosis, Renal Tubular, Type I", "RENAL TUBULAR ACIDOSIS, DISTAL 1", "Classical renal tubular acidosis", "familial distal primary acidosis", "Familial distal primary acidosis", "RENAL TUBULAR ACIDOSIS, DISTAL, 1", "Albright's renal tubular acidosis", "SWANN BLOOD GROUP ANTIGEN PHENOTYPE", "DIEGO BLOOD GROUP ANTIGEN PHENOTYPE", "RENAL TUBULAR ACIDOSIS DISTAL TYPE 1", "CRYOHYDROCYTOSIS DUE TO BAND 3 HEMEL", "type I distal renal tubular acidosis", "RTA, Distal Type, Autosomal Dominant", "RTA, DISTAL TYPE, AUTOSOMAL DOMINANT", "Renal tubular acidosis, type 1 distal", "Classic distal renal tubular acidosis", "Classic Distal Renal Tubular Acidosis", "RENAL TUBULAR ACIDOSIS DISTAL <TYPE 1>", "distal (type I) renal tubular acidosis", "Renal tubular acidosis, gradient defect", "distal renal tubular acidosis (disease)", "Distal renal tubular acidosis (disorder)", "CRYOHYDROCYTOSIS DUE TO BAND 3 BLACKBURN", "hypokalemic distal renal tubular acidosis", "Hypokalemic distal renal tubular acidosis", "SPHEROCYTOSIS, TYPE 4, DUE TO BAND 3 LYON", "SPHEROCYTOSIS, TYPE 4, DUE TO BAND 3 CHUR", "RTA Type I - Type I renal tubular acidosis", "SPHEROCYTOSIS, TYPE 4, DUE TO BAND 3 TOKYO", "SPHEROCYTOSIS, TYPE 4, DUE TO BAND 3 GENAS", "Hypokalaemic distal renal tubular acidosis", "SPHEROCYTOSIS, TYPE 4, DUE TO BAND 3 PRAGUE", "SPHEROCYTOSIS, TYPE 4, DUE TO BAND 3 COIMBRA", "SPHEROCYTOSIS, TYPE 4, DUE TO BAND 3 FUKUOKA", "CRYOHYDROCYTOSIS DUE TO BAND 3 HURSTPIERPOINT", "SPHEROCYTOSIS, TYPE 4, DUE TO BAND 3 CAPE TOWN", "SPHEROCYTOSIS, TYPE 4, DUE TO BAND 3 PRAGUE II", "SPHEROCYTOSIS, TYPE 4, DUE TO BAND 3 NOIRTERRE", "SPHEROCYTOSIS, TYPE 4, DUE TO BAND 3 MONTEFIORE", "SPHEROCYTOSIS, TYPE 4, DUE TO BAND 3 PRAGUE III", "SPHEROCYTOSIS, TYPE 4, DUE TO BAND 3 TUSCALOOSA", "type I distal renal tubular acidosis (diagnosis)", "Autosomal Dominant Distal Renal Tubular Acidosis", "Autosomal dominant distal renal tubular acidosis", "Renal Tubular Acidosis, Distal, Autosomal Dominant", "Hypokalemic distal renal tubular acidosis (diagnosis)", "RENAL TUBULAR ACIDOSIS, DISTAL 4, WITH HEMOLYTIC ANEMIA", "RENAL TUBULAR ACIDOSIS, DISTAL, 4, WITH HEMOLYTIC ANEMIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal renal tubular acidosis", "shortest_name_length": 2}
{"curie": "UMLS:C0568180", "names": ["Lithium toxicity", "lithium toxicity", "LITHIUM TOXICITY", "Lithium poisoning", "lithium poisoning", "lithium toxicities", "LITHIUM INTOXICATION", "poisoning by lithium", "lithium intoxication", "Lithium poisoning (disorder)", "poisoning by lithium (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lithium poisoning", "shortest_name_length": 16}
{"curie": "UMLS:C0266414", "names": ["Imperforate Vagina", "Imperforate vagina", "IMPERFORATE VAGINA", "imperforate; vagina", "vagina; imperforate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Imperforate Vagina", "shortest_name_length": 18}
{"curie": "UMLS:C0451833", "names": ["Staphylococcal arthritis or polyarthritis", "Staphylococcal arthritis and polyarthritis", "Arthritis or Polyarthritis due to Staphylococcus", "Arthritis or polyarthritis due to staphylococcus", "Staphylococcal arthritis and polyarthritis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Staphylococcal arthritis and polyarthritis", "shortest_name_length": 41}
{"curie": "MONDO:0000890", "names": ["congenital Zika syndrome", "ZIKV congenital infection", "Zika virus congenital syndrome", "congenital Zika virus infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Zika virus congenital syndrome", "shortest_name_length": 24}
{"curie": "UMLS:C3898649", "names": ["Juvenile Localized Scleroderma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Juvenile Localized Scleroderma", "shortest_name_length": 30}
{"curie": "MONDO:0024457", "names": ["PLAN", "INAD", "inaD", "INAD1", "NBIA2A", "NBIA2a", "PLA2G6-Related NBIA", "NBIA, PLA2G6-Related", "NBIA, PLA2G6 Related", "Seitelberger disease", "Seitelberger Disease", "SEITELBERGER DISEASE", "Disease, Seitelberger", "Seitelbergers Disease", "Seitelberger's disease", "seitelberger's disease", "Seitelberger's Disease", "Disease, Seitelberger's", "KARAK syndrome, included", "infantile neuroaxonal dystrophy", "Spastic amaurotic axonal idiocy", "Infantile Neuroaxonal Dystrophy", "Infantile neuroaxonal dystrophy", "neuroaxonal dystrophy, infantile", "Neuroaxonal Dystrophy, Infantile", "Dystrophy, Infantile Neuroaxonal", "NEUROAXONAL DYSTROPHY, INFANTILE", "Infantile Neuroaxonal Dystrophy 1", "infantile neuroaxonal dystrophy 1", "Hunter-Carpenter-McDonald syndrome", "Hunter Carpenter Macdonald syndrome", "PLA2G6-associated neurodegeneration", "PLA2G6-Associated Neurodegeneration", "neurodegeneration, Pla2g6-associated", "neurodegeneration, PLA2G6-associated", "Neurodegeneration, PLA2G6-Associated", "Neurodegeneration, Pla2g6-Associated", "neurodegeneration, Pla2G6-associated", "Neurodegeneration, PLA2G6 Associated", "NEURODEGENERATION, PLA2G6-ASSOCIATED", "INAD - Infantile neuroaxonal dystrophy", "Infantile neuroaxonal dystrophy (disorder)", "phospholipase A2-associated neurodegeneration", "Phospholipase A2-associated neurodegeneration", "Neurodegeneration With Brain Iron Accumulation 2A", "neurodegeneration with brain iron accumulation 2a", "neurodegeneration with brain iron accumulation 2A", "NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A", "neurodegeneration with brain iron accumulation type 2a", "neurodegeneration with brain iron accumulation type 2A", "infantile neuroaxonal dystrophy/atypical neuroaxonal dystrophy", "neuroaxonal dystrophy presenting with neonatal dysmorphic features, early onset of peripheral gangrene"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodegeneration with brain iron accumulation 2A", "shortest_name_length": 4}
{"curie": "MONDO:0021824", "names": ["adult SMA Aran Duchenne type", "Aran Duchenne spinal muscular atrophy", "adult progressive spinal muscular atrophy Aran Duchenne type", "adult progressive spinal muscular atrophy, Aran Duchenne type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult progressive spinal muscular atrophy, Aran Duchenne type", "shortest_name_length": 28}
{"curie": "UMLS:C1332050", "names": ["AIDS-Related Malignant Cervix Tumor", "AIDS-Related Malignant Cervical Tumor", "AIDS-Related Malignant Cervix Neoplasm", "AIDS-Related Malignant Tumor of Cervix", "AIDS-Related Malignant Cervical Neoplasm", "AIDS-Related Malignant Neoplasm of Cervix", "AIDS-Related Malignant Cervix Uteri Tumor", "AIDS-Related Malignant Tumor of the Cervix", "AIDS-Related Malignant Uterine Cervix Tumor", "AIDS-Related Malignant Tumor of Cervix Uteri", "AIDS-Related Malignant Cervix Uteri Neoplasm", "AIDS-Related Malignant Neoplasm of the Cervix", "AIDS-Related Malignant Uterine Cervix Neoplasm", "AIDS-Related Malignant Tumor of Uterine Cervix", "AIDS-Related Malignant Neoplasm of Cervix Uteri", "AIDS-Related Malignant Tumor of the Cervix Uteri", "AIDS-Related Malignant Neoplasm of Uterine Cervix", "AIDS-Related Malignant Tumor of the Uterine Cervix", "AIDS-Related Malignant Neoplasm of the Cervix Uteri", "AIDS-Related Malignant Neoplasm of the Uterine Cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Malignant Cervical Neoplasm", "shortest_name_length": 35}
{"curie": "MONDO:0011499", "names": ["OKAMOTO SYNDROME", "Okamoto syndrome", "Okamoto Syndrome", "Okamoto syndrome (disorder)", "Okamoto syndrome (diagnosis)", "congenital hydronephrosis with cleft palate, characteristic facies, hypotonia, and mental retardation", "Hydronephrosis, Congenital, with Cleft Palate, Characteristic Facies, Hypotonia, and Mental Retardation", "hydronephrosis, congenital, with cleft palate, characteristic facies, hypotonia, and mental retardation", "HYDRONEPHROSIS, CONGENITAL, WITH CLEFT PALATE, CHARACTERISTIC FACIES, HYPOTONIA, AND MENTAL RETARDATION", "congenital hydronephrosis with cleft palate, characteristic facies, hypotonia, and intellectual disability", "hydronephrosis, congenital, with cleft palate, characteristic facies, hypotonia, and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Okamoto syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0004356", "names": ["childhood renal Wilms cancer", "benign multilocular cystic renal tumor", "benign Multilocular cystic renal tumor", "pediatric Multilocular cystic renal tumor", "pediatric multilocular cystic renal tumor", "Childhood Multilocular Cystic Renal Tumor", "childhood multilocular cystic renal tumor", "Pediatric Multilocular Cystic Renal Tumor", "pediatric multilocular cystic kidney tumor", "Pediatric Multilocular Cystic Kidney Tumor", "Childhood Multilocular Cystic Kidney Tumor", "childhood multilocular cystic kidney tumor", "pediatric multilocular cystic renal neoplasm", "childhood multilocular cystic renal neoplasm", "Pediatric Multilocular Cystic Renal Neoplasm", "Childhood Multilocular Cystic Renal Neoplasm", "childhood multilocular cystic kidney neoplasm", "Childhood Multilocular Cystic Kidney Neoplasm", "pediatric multilocular cystic kidney neoplasm", "Pediatric Multilocular Cystic Kidney Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood multilocular cystic kidney neoplasm", "shortest_name_length": 28}
{"curie": "UMLS:C1335734", "names": ["Regressing Non-Cutaneous Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Regressing Non-Cutaneous Melanoma", "shortest_name_length": 33}
{"curie": "UMLS:C1561246", "names": ["Head soft tissue necrosis", "necrosis soft tissue head", "necrosis of soft tissue of head", "Head Soft Tissue Necrotic Lesion", "necrosis of soft tissue of head (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Head soft tissue necrosis", "shortest_name_length": 25}
{"curie": "UMLS:C5420857", "names": ["Resectable Pancreatic Adenosquamous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Pancreatic Adenosquamous Carcinoma", "shortest_name_length": 45}
{"curie": "UMLS:C4525407", "names": ["Refractory Ph-Like Acute Lymphoblastic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Ph-Like Acute Lymphoblastic Leukemia", "shortest_name_length": 47}
{"curie": "UMLS:C0472383", "names": ["Spontaneous Subarachnoid Hemorrhage", "Spontaneous subarachnoid hemorrhage", "subarachnoid hemorrhage spontaneous", "Spontaneous subarachnoid haemorrhage", "Spontaneous Subarachnoid Hemorrhages", "Subarachnoid Hemorrhage, Spontaneous", "Hemorrhage, Spontaneous Subarachnoid", "Hemorrhages, Spontaneous Subarachnoid", "Subarachnoid Hemorrhages, Spontaneous", "SAH - Spontaneous subarachnoid hemorrhage", "SAH - Spontaneous subarachnoid haemorrhage", "Spontaneous subarachnoid hemorrhage (diagnosis)", "Spontaneous intracranial subarachnoid hemorrhage", "Spontaneous intracranial subarachnoid haemorrhage", "Nontraumatic subarachnoid intracranial hemorrhage", "Nontraumatic subarachnoid intracranial haemorrhage", "Spontaneous intracranial subarachnoid hemorrhage (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subarachnoid Hemorrhage, Spontaneous", "shortest_name_length": 35}
{"curie": "MONDO:0024299", "names": ["VDDR", "Active rickets", "Rickets, active", "Active rickets (disorder)", "vitamin D dependent rickets", "vitamin D-dependent rickets", "Vitamin D-dependent rickets", "Vitamin D-dependent rickets, NOS", "VDDRI - Vitamin D-dependent rickets", "Vitamin D-dependent rickets (disorder)", "vitamin D dependent rickets (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitamin D-dependent rickets", "shortest_name_length": 4}
{"curie": "MONDO:0004258", "names": ["anorgasmia female", "female anorgasmia", "Female anorgasmia", "inhibited female orgasm", "Inhibited female orgasm", "Female orgasmic disorder", "female orgasmic disorder", "Female Orgasmic Disorder", "disorder female orgasmic", "female Orgasmic disorder", "female anorgasmia (diagnosis)", "Inhibited female orgasm (disorder)", "Inhibited female orgasm, psychogenic", "female orgasmic disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "female orgasmic disorder", "shortest_name_length": 17}
{"curie": "MONDO:0011130", "names": ["Sebaceous gland hyperplasia, familial presenile", "SEBACEOUS GLAND HYPERPLASIA, FAMILIAL PRESENILE", "sebaceous gland hyperplasia, familial presenile"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sebaceous gland hyperplasia, familial presenile", "shortest_name_length": 47}
{"curie": "UMLS:C5239012", "names": ["Cutaneous Burkitt Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous Burkitt Lymphoma", "shortest_name_length": 26}
{"curie": "MONDO:0021389", "names": ["Aortic body tumor", "aortic body tumor", "Aortic Body Tumor", "tumor; aortic body", "Aortic body tumour", "tumor of aortic body", "Aortic Body Neoplasm", "[M]Aortic body tumor", "aortic body neoplasm", "Tumor of Aortic Body", "[M]Aortic body tumour", "neoplasm of aortic body", "Neoplasm of Aortic Body", "Neoplasm of aortic body", "Tumor of the Aortic Body", "tumor of the aortic body", "Aortic body paraganglioma", "aortic body paraganglioma", "Aortic Body Paraganglioma", "paraganglioma; aortic body", "Neoplasm of the Aortic Body", "neoplasm of the aortic body", "paraganglioma of aortic body", "Paraganglioma of Aortic Body", "Aorticopulmonary Paraganglioma", "aortic body neoplasm (disease)", "aorticopulmonary paraganglioma", "Aorticopulmonary paraganglioma", "paraganglioma of the aortic body", "Paraganglioma of the Aortic Body", "Neoplasm of aortic body (disorder)", "neoplasm of aortic body (diagnosis)", "Aortic body tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplasm of aortic body", "shortest_name_length": 17}
{"curie": "MONDO:0012544", "names": ["Bdsd", "BDSD", "BDSDO", "Brachydactyly-Syndactyly Syndrome", "BRACHYDACTYLY-SYNDACTYLY SYNDROME", "brachydactyly-syndactyly syndrome", "brachydactyly-syndactyly, Zhao type", "brachydactyly-syndactyly-oligodactyly syndrome", "BRACHYDACTYLY-SYNDACTYLY-OLIGODACTYLY SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly-syndactyly syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0038048", "names": ["sprain strain", "strain sprain", "Sprain/strain", "sprains strain", "sprain strains", "sprain (strain)", "strains sprains", "sprains strains", "Sprains and Strains", "Strains and Sprains", "SPRAINS AND STRAINS", "Sprains and strains", "SPRAINS AND STRAINS OF JOINTS AND ADJACENT MUSCLES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sprains and Strains", "shortest_name_length": 13}
{"curie": "MONDO:0018134", "names": ["disorder of melanin metabolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of melanin metabolism", "shortest_name_length": 30}
{"curie": "MONDO:0014222", "names": ["APDS", "IMD14", "PASLI disease", "immunodeficiency 14", "immunodeficiency type 14", "activated PI3K-delta syndrome", "Activated PI3K-Delta syndrome", "immunodeficiency 14A, autosomal dominant", "p110-Delta-Activating mutation causing senescent T cells, lymphadenopathy, and immunodeficiency", "senescent T-cells-lymphadenopathy-immunodeficiency syndrome due to p110delta-activating mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 14", "shortest_name_length": 4}
{"curie": "UMLS:C2828035", "names": ["Stage IIIB Skin Melanoma AJCC v7", "Stage IIIB Cutaneous (Skin) Melanoma", "Stage IIIB Cutaneous Melanoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Cutaneous Melanoma AJCC v7", "shortest_name_length": 32}
{"curie": "UMLS:C0085598", "names": ["False labor", "false labor", "False Labor", "false labour", "labor; false", "false; labor", "Labour;false", "Labor, false", "LABOR, FALSE", "False labour", "Spurious labor", "Spurious labour", "False labor (finding)", "Threatened Term Labor", "pregnancy; false labor", "false labor (diagnosis)", "False labor, unspecified", "False labour, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "False labor", "shortest_name_length": 11}
{"curie": "MONDO:0013147", "names": ["CMD1CC", "dilated cardiomyopathy 1CC", "cardiomyopathy, dilated, 1CC", "Cardiomyopathy, Dilated, 1CC", "CARDIOMYOPATHY, DILATED, 1CC", "dilated cardiomyopathy type 1CC", "cardiomyopathy, dilated, type 1Cc", "NEXN familial isolated dilated cardiomyopathy", "familial isolated dilated cardiomyopathy caused by mutation in NEXN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1CC", "shortest_name_length": 6}
{"curie": "UMLS:C0001707", "names": ["aerophagy", "Aerophagy", "AEROPHAGIA", "Aerophagia", "aerophagia", "air swallow", "swallow air", "swallowing air", "Air Swallowing", "air swallowing", "Air swallowing", "Swallowing, Air", "Aerophagy (finding)", "Psychogenic aerophagy", "Psychogenic aerophagia", "swallowing air (history)", "Air swallowing - excessive", "Aerophagy (swallowing air)", "Excessive swallowing of air"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aerophagy", "shortest_name_length": 9}
{"curie": "UMLS:C1332947", "names": ["Grade 3 Childhood Brain Astrocytoma", "Grade 3 Pediatric Brain Astrocytoma", "Grade III Pediatric Brain Astrocytoma", "Grade III Childhood Brain Astrocytoma", "Grade 3 Pediatric Astrocytoma of Brain", "Anaplastic Childhood Brain Astrocytoma", "Childhood Brain Anaplastic Astrocytoma", "Anaplastic Pediatric Brain Astrocytoma", "Grade 3 Childhood Astrocytoma of Brain", "Grade 3 Childhood Brain Astrocytic Tumor", "Grade III Childhood Astrocytoma of Brain", "Grade 3 Pediatric Brain Astrocytic Tumor", "Grade III Pediatric Astrocytoma of Brain", "Anaplastic Pediatric Astrocytoma of Brain", "Anaplastic Childhood Astrocytoma of Brain", "Grade III Pediatric Brain Astrocytic Tumor", "Grade 3 Pediatric Astrocytoma of the Brain", "Grade 3 Childhood Astrocytoma of the Brain", "Grade III Childhood Brain Astrocytic Tumor", "Grade 3 Pediatric Brain Astrocytic Neoplasm", "Grade 3 Childhood Brain Astrocytic Neoplasm", "Grade 3 Pediatric Astrocytic Tumor of Brain", "Grade 3 Childhood Astrocytic Tumor of Brain", "Grade III Childhood Astrocytoma of the Brain", "Grade III Pediatric Astrocytoma of the Brain", "Grade III Childhood Astrocytic Tumor of Brain", "Grade III Pediatric Brain Astrocytic Neoplasm", "Anaplastic Pediatric Astrocytoma of the Brain", "Grade III Childhood Brain Astrocytic Neoplasm", "Grade III Pediatric Astrocytic Tumor of Brain", "Anaplastic Childhood Astrocytoma of the Brain", "Grade 3 Pediatric Astrocytic Neoplasm of Brain", "Grade 3 Childhood Astrocytic Neoplasm of Brain", "Grade 3 Childhood Astrocytic Tumor of the Brain", "Grade 3 Pediatric Astrocytic Tumor of the Brain", "Grade III Pediatric Astrocytic Neoplasm of Brain", "Grade III Childhood Astrocytic Neoplasm of Brain", "Grade III Childhood Astrocytic Tumor of the Brain", "Grade III Pediatric Astrocytic Tumor of the Brain", "Grade 3 Childhood Astrocytic Neoplasm of the Brain", "Grade 3 Pediatric Astrocytic Neoplasm of the Brain", "Grade III Childhood Astrocytic Neoplasm of the Brain", "Grade III Pediatric Astrocytic Neoplasm of the Brain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Brain Anaplastic Astrocytoma", "shortest_name_length": 35}
{"curie": "MONDO:0001086", "names": ["partial optic atrophy", "Partial optic atrophy", "Partial optic atrophy (disorder)", "partial optic atrophy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial optic atrophy", "shortest_name_length": 21}
{"curie": "UMLS:C0877090", "names": ["Orthostatic collapse"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Orthostatic collapse", "shortest_name_length": 20}
{"curie": "UMLS:C4745308", "names": ["Recurrent Endometrial Undifferentiated Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Endometrial Undifferentiated Carcinoma", "shortest_name_length": 48}
{"curie": "UMLS:C0155843", "names": ["retropharyngeal abscess", "Retropharyngeal abscess", "Retropharyngeal Abscess", "RETROPHARYNGEAL ABSCESS", "abscess retropharyngeal", "abscess; retropharyngeal", "Abscess, Retropharyngeal", "ABSCESS, RETROPHARYNGEAL", "retropharyngeal; abscess", "Retro-pharyngeal abscess", "Retropharyngeal Abscesses", "Abscesses, Retropharyngeal", "Retro-pharyngeal abscess NOS", "Retropharyngeal abscess (disorder)", "retropharyngeal abscess (diagnosis)", "retropharyngeal abscess (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retropharyngeal Abscess", "shortest_name_length": 23}
{"curie": "MONDO:0011988", "names": ["IMD73A", "NEUTROPHIL IMMUNODEFICIENCY SYNDROME", "Neutrophil Immunodeficiency Syndrome", "Neutrophil immunodeficiency syndrome", "neutrophil immunodeficiency syndrome", "Neutrophil immunodeficiency syndrome (disorder)", "IMMUNODEFICIENCY 73A WITH DEFECTIVE NEUTROPHIL CHEMOTAXIS AND LEUKOCYTOSIS", "immunodeficiency 73A with defective neutrophil chemotaxix and leukocytosis", "immunodeficiency 73a with defective neutrophil chemotaxis and leukocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neutrophil immunodeficiency syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C3272259", "names": ["SPONTANEOUS SUSTAINED VENTRICULAR TACHYCARDIA", "Spontaneous Sustained Ventricular Tachycardia", "Spontaneous Sustained Ventricular Tachycardia by EKG Finding", "Spontaneous Sustained Ventricular Tachycardia by ECG Finding"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spontaneous Sustained Ventricular Tachycardia by ECG Finding", "shortest_name_length": 45}
{"curie": "MONDO:0002721", "names": ["NECROSIS PITUITARY", "pituitary necrosis", "Pituitary Necrosis", "Necrosis pituitary", "Pituitary necrosis", "necrosis; pituitary", "pituitary; necrosis", "Necrosis of pituitary", "necrosis of pituitary", "pituitary gland Necrosis", "Pituitary Gland Necrosis", "Necrosis of pituitary, NOS", "necrosis of pituitary gland", "Necrosis of pituitary (disorder)", "necrosis of pituitary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "necrosis of pituitary", "shortest_name_length": 18}
{"curie": "UMLS:C0751636", "names": ["External carotid artery stenosis", "External Carotid Artery Stenosis", "Stenosis, External Carotid Artery"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "External Carotid Artery Stenosis", "shortest_name_length": 32}
{"curie": "MONDO:0014402", "names": ["PELD", "severe neurodegenerative syndrome with lipodystrophy", "severe neurodegenerative syndrome due to BSCL2 deficiency", "encephalopathy, progressive, with or without lipodystrophy", "ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe neurodegenerative syndrome with lipodystrophy", "shortest_name_length": 4}
{"curie": "UMLS:C1333631", "names": ["Foregut Carcinoid Tumor", "Foregut Neuroendocrine Tumor G1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Foregut Neuroendocrine Tumor G1", "shortest_name_length": 23}
{"curie": "UMLS:C1333503", "names": ["Extrahepatic Bile Duct NET G1", "Extrahepatic Bile Duct Carcinoid Tumor", "Carcinoid Tumor of Extrahepatic Bile Duct", "Carcinoid Tumor of the Extrahepatic Bile Duct", "Extrahepatic Bile Duct Neuroendocrine Tumor G1", "malignant carcinoid tumor of extrahepatic bile duct", "Extrahepatic Bile Duct Neuroendocrine Tumor G1 (Carcinoid)", "malignant carcinoid tumor of extrahepatic bile duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extrahepatic Bile Duct Carcinoid Tumor", "shortest_name_length": 29}
{"curie": "UMLS:C0018949", "names": ["Hematomyelia", "hematomyelia", "Haematomyelia", "Hematomyelias", "Spinal cord bleeding", "SPINAL CORD HEMORRHAGE", "Spinal cord hemorrhage", "spinal cord hemorrhage", "Spinal Cord Hemorrhage", "Spinal cord haemorrhage", "Hematomyelia (disorder)", "hemorrhage; spinal cord", "spinal cord; hemorrhage", "hematomyelia (diagnosis)", "Intramedullary hemorrhage", "Hemorrhage of spinal cord", "hemorrhage; intramedullary", "intramedullary; hemorrhage", "Intramedullary haemorrhage", "Hemorrhage of spinal cord (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hematomyelia", "shortest_name_length": 12}
{"curie": "UMLS:C3898092", "names": ["Oral Complication", "oral complications"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral Complication", "shortest_name_length": 17}
{"curie": "MONDO:0003235", "names": ["Optic glioma", "optic glioma", "Optic Glioma", "glioma optic", "OPTIC GLIOMA", "Optic Gliomas", "optic gliomas", "Optic gliomas", "Glioma, Optic", "Gliomas, Optic", "optic nerve glioma", "Optic Nerve Glioma", "Optic nerve glioma", "Optic Nerve Gliomas", "Glioma, Optic Nerve", "Gliomas, Optic Nerve", "glioma of optic nerve", "Glioma of Optic Nerve", "cranial nerve II glioma", "Optic glioma (diagnosis)", "optic nerve glioblastoma", "Glioma of the Optic Nerve", "glioma of the optic nerve", "glioma of cranial nerve II", "Optic nerve glioma (disorder)", "glioma of optic nerve (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "optic nerve glioma", "shortest_name_length": 12}
{"curie": "UMLS:C1168204", "names": ["stage IVA pancreatic cancer", "Stage IVA Pancreatic Cancer", "pancreatic cancer, stage IVA", "Stage IVA Pancreatic Carcinoma", "Pancreatic carcinoma stage IVA", "Stage IVA Carcinoma of Pancreas", "Stage IVA Carcinoma of the Pancreas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic carcinoma stage IVA", "shortest_name_length": 27}
{"curie": "MONDO:0013938", "names": ["CG8", "CGA", "PBD7A", "peroxisome biogenesis disorder 7A", "Peroxisome Biogenesis Disorder 7A", "peroxisome biogenesis disorder 7A (Zellweger)", "PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER)", "peroxisome biogenesis disorder, complementation group A", "PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 8", "PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP A", "peroxisome biogenesis disorder, complementation group 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder 7A (Zellweger)", "shortest_name_length": 3}
{"curie": "MONDO:0700149", "names": ["canine sarcoma", "Canine Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canine sarcoma", "shortest_name_length": 14}
{"curie": "MONDO:0021698", "names": ["alcohol disorders", "alcoholism syndrome", "alcohol-related disorder", "Alcohol-Related Disorder", "alcohol related disorder", "Alcohol-Related Disorders", "alcohol related disorders", "Alcohol related disorders", "alcohol-related disorders", "Alcohol Related Disorders", "Disorder, Alcohol-Related", "disorder, alcohol-related", "Alcohol-related disorders", "disorders, alcohol-related", "Alcohol-related disorder NOS", "unspecified alcohol related disorder", "Unspecified alcohol-related disorder", "alcohol-related disorders (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alcohol-related disorders", "shortest_name_length": 17}
{"curie": "MONDO:0017466", "names": ["congenital pseudarthrosis of the ulna", "congenital pseudoarthrosis of the ulna"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital pseudoarthrosis of the ulna", "shortest_name_length": 37}
{"curie": "UMLS:C5205120", "names": ["Advanced NUT Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced NUT Carcinoma", "shortest_name_length": 22}
{"curie": "MONDO:0015303", "names": ["Macular amyloidosis", "macular amyloidosis", "Amyloidosis, macular", "macular; amyloidosis (manifestation)", "amyloidosis; macular (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macular amyloidosis", "shortest_name_length": 19}
{"curie": "MONDO:0009922", "names": ["Pseudouridinuria and Mental Defect", "PSEUDOURIDINURIA AND MENTAL DEFECT", "Pseudouridinuria and mental defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pseudouridinuria and mental defect", "shortest_name_length": 34}
{"curie": "UMLS:C5669721", "names": ["Transformed Waldenstrom Macroglobulinemia to Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transformed Waldenstrom Macroglobulinemia to Diffuse Large B-Cell Lymphoma", "shortest_name_length": 74}
{"curie": "UMLS:C4524313", "names": ["Stage IIA Uterine Sarcoma", "Stage IIA Uterine Sarcoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Uterine Sarcoma AJCC v7", "shortest_name_length": 25}
{"curie": "MONDO:0014412", "names": ["Familial GPIHBP1 deficiency", "familial GPIHBP1 deficiency", "hyperlipoproteinemia type 1D", "hyperlipoproteinemia type ID", "HYPERLIPOPROTEINEMIA, TYPE ID", "hyperlipoproteinemia, type 1D", "hyperlipoproteinemia, type ID", "GPIHBP1 familial hyperlipidemia", "familial hyperlipidemia caused by mutation in GPIHBP1", "Familial glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1 deficiency", "familial glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperlipoproteinemia, type 1D", "shortest_name_length": 27}
{"curie": "MONDO:0015000", "names": ["DEE48", "EIEE48", "early infantile epileptic encephalopathy 48", "epileptic encephalopathy, early infantile, 48", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 48", "developmental and epileptic encephalopathy 48", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 48", "AP3B2 early infantile epileptic encephalopathy", "developmental and epileptic encephalopathy, 48", "epileptic encephalopathy, early infantile, type 48", "epileptic encephalopathy, early infantile, 48; EIEE48", "early infantile epileptic encephalopathy caused by mutation in AP3B2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 48", "shortest_name_length": 5}
{"curie": "MONDO:0018975", "names": ["NF1", "FSNF", "Neurofibromatosis", "neurofibromatosis", "Molluscum Fibrosum", "Neurofibromatosis I", "neurofibromatosis i", "neurofibromatosis 1", "Neurofibromatosis 1", "Recklinghausen disease", "RECKLINGHAUSEN DISEASE", "recklinghausen disease", "disease recklinghausens", "Type 1 Neurofibromatosis", "recklinghausen's disease", "type 1 neurofibromatosis", "NEUROFIBROMATOSIS TYPE 1", "Neurofibromatosis type 1", "neurofibromatosis type 1", "neurofibromatosis type i", "type I neurofibromatosis", "neurofibromatosis type I", "Neurofibromatosis Type 1", "Neurofibromatosis Type I", "Recklinghausen's disease", "Type I Neurofibromatoses", "von Reklinghausen disease", "Neurofibromatosis, Type I", "NF1 (Neurofibromatosis 1)", "NEUROFIBROMATOSIS, TYPE I", "Neurofibromatosis, type 1", "neurofibromatosis, type 1", "Neurofibromatoses, Type I", "Neurofibromatosis, Type 1", "Type 1, Neurofibromatosis", "neurofibromatosis, type I", "Type I, Neurofibromatosis", "Nf1-Microdeletion syndrome", "Von Recklinghausen Disease", "von Recklinghausen Disease", "von recklinghausen disease", "VON RECKLINGHAUSEN DISEASE", "Von Recklinghausen disease", "von recklinghausens disease", "PHAKOMATOSIS RECKLINGHAUSEN", "von Recklinghausens Disease", "Von Recklinghausen; disease", "disease; Von Recklinghausen", "Peripheral Neurofibromatosis", "von Recklinghausen's disease", "von Recklinghausen's Disease", "Peripheral Neurofibromatoses", "Von Recklinghausen's Disease", "von recklinghausen's disease", "peripheral neurofibromatosis", "Neurofibromatosis, Peripheral", "Neurofibromatoses, Peripheral", "Recklinghausen Disease, Nerve", "NF1 - Neurofibromatosis type 1", "Recklinghausen Disease of Nerve", "Recklinghausens Disease of Nerve", "Recklinghausen's Disease of Nerve", "familial spinal neurofibromatosis", "Neurofibromatosis, Peripheral Type", "Neurofibromatosis, Peripheral, NF1", "NEUROFIBROMATOSIS, PERIPHERAL TYPE", "Neurofibromatosis, peripheral type", "Recklinghausen's neurofibromatosis", "neurofibromatosis, peripheral type", "Multiple non-ossifying fibromatosis", "Neurofibromatosis, Peripheral, NF 1", "Neurofibromatosis type 1 (disorder)", "type I neurofibromatosis (diagnosis)", "Clinical von Reclinghausen's disease", "Von Recklinghausen's disease (of nerve)", "Neurofibromatosis Type 1 Microdeletion Syndrome", "neurofibromatosis type 1 microdeletion syndrome", "neurofibromatosis type I (von Recklinghausen's disease)", "Neurofibromatosis, type 1 (von Recklinghausen's disease)", "Neurofibromatosis, type 1 [von recklinghausen's disease]", "Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion", "Von Recklinghausen disease due to NF1 mutation or intragenic deletion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurofibromatosis type 1", "shortest_name_length": 3}
{"curie": "UMLS:C0862793", "names": ["Stage IIIB Lung Adenocarcinoma", "adenocarcinoma iiib lung stage", "Adenocarcinoma of lung stage IIIB", "adenocarcinoma of lung stage iiib", "Stage IIIB Adenocarcinoma of Lung", "Stage IIIB Adenocarcinoma of the Lung", "Stage IIIB Lung Adenocarcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma of lung stage IIIB", "shortest_name_length": 30}
{"curie": "UMLS:C5238485", "names": ["Microinvasive Anal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Microinvasive Anal Carcinoma", "shortest_name_length": 28}
{"curie": "UMLS:C3897753", "names": ["Recurrent Giant Cell Glioblastoma", "recurrent childhood giant cell glioblastoma", "Recurrent Childhood Giant Cell Glioblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Giant Cell Glioblastoma", "shortest_name_length": 33}
{"curie": "UMLS:C4708088", "names": ["gBRCA-mutated, HER2(-) metastatic breast carcinoma", "Germline BRCA-mutated, HER2-negative metastatic breast cancer", "Germline BRCA-mutated human epidermal growth factor receptor 2 negative metastatic carcinoma of breast", "Germline BRCA-mutated human epidermal growth factor receptor 2 negative metastatic carcinoma of breast (disorder)", "Germline BRCA-mutated human epidermal growth factor receptor 2 negative metastatic carcinoma of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Germline BRCA-mutated, HER2-negative metastatic breast cancer", "shortest_name_length": 50}
{"curie": "MONDO:0001125", "names": ["Gonococcal epididymo-orchitis", "Acute gonococcal epididymo-orchitis", "acute gonococcal epididymo-orchitis", "gonococcal epididymo-orchitis, acute", "Gonococcal epididymo-orchitis (acute)", "gonococcal epididymo-orchitis (acute)", "Acute gonococcal epididymo-orchitis (disorder)", "acute gonococcal epididymo-orchitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute gonococcal epididymo-orchitis", "shortest_name_length": 29}
{"curie": "MONDO:0021569", "names": ["EMD2", "EDMD2", "LGMD1B", "LGMD1B, FORMERLY", "Emery-Dreifuss muscular dystrophy 2", "Emery-Dreifuss Muscular Dystrophy 2", "Emery Dreifuss Muscular Dystrophy 2", "proximal muscular dystrophy type 1B", "Muscular dystrophy, proximal, type 1B", "muscular dystrophy, proximal, type 1B", "limb-girdle muscular dystrophy type 1B", "Limb-girdle muscular dystrophy, type 1B", "muscular dystrophy, limb-girdle type 1B", "Muscular Dystrophy, Limb-Girdle, Type 1B", "HAUPTMANN-THANNHAUSER MUSCULAR DYSTROPHY", "Hauptmann-Thannhauser Muscular Dystrophy", "Hauptmann Thannhauser Muscular Dystrophy", "muscular dystrophy, limb-girdle, type 1B", "Hauptmann-Thannhauser muscular dystrophy", "scapuloilioperoneal atrophy with cardiopathy", "Scapuloilioperoneal Atrophy with Cardiopathy", "SCAPULOILIOPERONEAL ATROPHY WITH CARDIOPATHY", "Emery-Dreifuss muscular dystrophy 2 (diagnosis)", "MUSCULAR DYSTROPHY, PROXIMAL, TYPE 1B, FORMERLY", "CARDIOMYOPATHY, DILATED, WITH QUADRICEPS MYOPATHY", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1B, FORMERLY", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1B (disorder)", "Autosomal dominant Emery-Dreifuss muscular dystrophy", "Autosomal Dominant Emery-Dreifuss Muscular Dystrophy", "Autosomal Dominant Emery Dreifuss Muscular Dystrophy", "EMERY-DREIFUSS MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT", "Emery-Dreifuss Muscular Dystrophy, Autosomal Dominant", "Emery-Dreifuss muscular dystrophy, autosomal dominant", "Emery Dreifuss Muscular Dystrophy, Autosomal Dominant", "autosomal dominant Emery-Dreifuss muscular dystrophy 2", "Muscular Dystrophy, Emery-Dreifuss, Autosomal Dominant", "LMNA autosomal dominant limb-girdle muscular dystrophy", "EMERY-DREIFUSS MUSCULAR DYSTROPHY 2, AUTOSOMAL DOMINANT", "Emery-Dreifuss Muscular Dystrophy 2, Autosomal Dominant", "Emery-Dreifuss muscular dystrophy 2, autosomal dominant", "autosomal dominant limb-girdle muscular dystrophy type 1B", "limb-girdle muscular dystrophy due to lamin A/C deficiency", "EDMD2 - autosomal dominant Emery-Dreifuss muscular dystrophy", "benign scapuloperoneal muscular dystrophy with cardiomyopathy", "Benign scapuloperoneal muscular dystrophy with cardiomyopathy", "Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder)", "Autosomal dominant Emery-Dreifuss muscular dystrophy (disorder)", "autosomal dominant limb-girdle muscular dystrophy caused by mutation in LMNA", "muscular dystrophy with early contractures and cardiomyopathy, autosomal dominant", "Muscular Dystrophy With Early Contractures And Cardiomyopathy, Autosomal Dominant", "MUSCULAR DYSTROPHY WITH EARLY CONTRACTURES AND CARDIOMYOPATHY, AUTOSOMAL DOMINANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Emery-Dreifuss muscular dystrophy 2, autosomal dominant", "shortest_name_length": 4}
{"curie": "MONDO:0019374", "names": ["SCAR5", "CAMOS", "CAMOS syndrome", "spinocerebellar ataxia autosomal recessive 5", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 5", "Spinocerebellar ataxia, autosomal recessive 5", "SCAR5 - spinocerebellar ataxia autosomal recessive 5", "cerebellar ataxia with mental retardation optic atrophy and skin abnormalities", "Cerebellar ataxia with mental retardation, optic atrophy, and skin abnormalities", "Cerebellar ataxia-intellectual disability-optic atrophy-skin abnormalities syndrome", "cerebellar ataxia-intellectual disability-optic atrophy-skin abnormalities syndrome", "cerebellar ataxia with intellectual disability optic atrophy and skin abnormalities", "Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome", "CAMOS (cerebellar ataxia, mental retardation, optic atrophy, skin abnormalities) syndrome", "Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder)", "Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CAMOS syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0018543", "names": ["HYPOC", "hypocalcemia", "AD hypocalcemia", "Familial hypocalcemia", "Familial hypocalcaemia", "Hypocalcemia, Familial", "HYPOCALCEMIA, FAMILIAL", "Autosomal dominant hypocalcemia", "autosomal dominant hypocalcemia", "hypocalcemia, autosomal dominant", "Hypocalcemia, Autosomal Dominant", "Autosomal dominant hypocalcaemia", "Familial hypercalciuric hypocalcemia", "Familial Hypercalciuric Hypocalcemia", "Hypercalciuric Hypocalcemia, Familial", "Familial hypercalciuric hypocalcaemia", "Autosomal dominant hypoparathyroidism", "Autosomal Dominant Hypoparathyroidism", "Hypoparathyroidism, Autosomal Dominant", "Hypoparathyroidism - autosomal dominant", "Autosomal dominant hypocalcemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant hypocalcemia", "shortest_name_length": 5}
{"curie": "UMLS:C0877578", "names": ["Iatrogenic Cancer", "Therapy-Related Cancer", "Therapy Related Cancer", "Therapy-Related Cancers", "Cancer, Therapy-Related", "Cancers, Therapy-Related", "Treatment Related Cancer", "Treatment-Related Cancer", "Therapy-Associated Cancer", "Treatment-Related Cancers", "Therapy Associated Cancer", "Cancer, Treatment-Related", "Cancer, Therapy-Associated", "Therapy-Associated Cancers", "Cancers, Treatment-Related", "Cancers, Therapy-Associated", "Treatment Associated Cancer", "Treatment-Associated Cancer", "Cancer, Treatment-Associated", "Treatment-Associated Cancers", "Cancers, Treatment-Associated", "Therapy Related Malignant Tumor", "Therapy-Related Malignant Neoplasm", "Therapy Related Malignant Neoplasm", "Treatment related secondary malignancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Treatment related secondary malignancy", "shortest_name_length": 17}
{"curie": "UMLS:C0677693", "names": ["Stage II Diffuse Mixed Cell Lymphoma", "Contiguous Stage II Adult Diffuse Mixed Cell Lymphoma", "Contiguous Adult Diffuse Mixed Cell Lymphoma Stage II", "Stage II Contiguous Adult Diffuse Mixed Cell Lymphoma", "contiguous stage II adult diffuse mixed cell lymphoma", "contiguous adult diffuse mixed cell lymphoma stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Contiguous Adult Diffuse Mixed Cell Lymphoma", "shortest_name_length": 36}
{"curie": "UMLS:C4744700", "names": ["Locally Advanced Pancreatic Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Pancreatic Adenocarcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0020971", "names": ["GC Urethritis", "gc urethritis", "urethra; gonorrhea", "gonorrhea; urethra", "gonococcal; urethra", "urethra; gonococcal", "URETHRITIS GONOCOCCAL", "gonococcal urethritis", "Urethritis gonococcal", "Gonococcal urethritis", "Gonococcal Urethritis", "gonococcal; urethritis", "urethritis; gonococcal", "Urethritis gonococcal NOS", "URETHRITIS, GONORRHEAL, MALE", "Gonococcal urethritis (disorder)", "gonococcal urethritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gonococcal urethritis", "shortest_name_length": 13}
{"curie": "MONDO:0000988", "names": ["otorrhea", "Otorrhea", "Otorrhoea", "otorrhoea", "EAR DRAINAGE", "Ear Drainage", "ear discharge", "Ear discharge", "discharge ear", "Discharge;ear", "Otorrhea, NOS", "EAR DISCHARGE", "discharge ears", "discharge; ear", "ear; discharge", "discharges ear", "discharging ear", "Discharging ear", "Discharge of ear", "Otorrhea syndrome", "discharge from ear", "Discharge from ear", "DISCHARGE FROM EAR", "discharge from ears", "Otorrhea (disorder)", "Discharging ear NOS", "otorrhea (diagnosis)", "Otorrhea, unspecified", "Ear discharge present", "Discharge of ear, NOS", "Ear discharge (finding)", "Discharge from ear canal", "Finding of ear discharge", "Otorrhea, unspecified ear", "Observation of ear discharge", "discharge from ears (symptom)", "Drainage from external ear canal", "discharge from external ear canal", "Ear discharge present (situation)", "external auditory canal discharge", "Drainage from external ear canal, NOS", "discharge from external ear canal (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "discharging ear", "shortest_name_length": 8}
{"curie": "MONDO:0017010", "names": ["trisomy Xq", "Xq trisomy", "Xq+ syndrome", "Xq duplication", "Duplication Xq", "Dup(Xq) syndrome", "dup(Xq) syndrome", "partial trisomy Xq", "chromosome Xq trisomy", "Xq duplication syndrome", "chromosome Xq duplication", "duplication (Xq) syndrome", "partial trisomy of chromosome Xq", "chromosome Xq duplication syndrome", "Chromosome Xq duplication syndrome", "partial duplication of chromosome Xq", "partial trisomy of the long arm of chromosome X", "partial duplication of the long arm of chromosome X", "partial duplication of the long arm of chromosome type X"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of the long arm of chromosome X", "shortest_name_length": 10}
{"curie": "MONDO:0016873", "names": ["partial deletion of chromosome 8", "partial monosomy of chromosome 8", "partial deletion of chromosome type 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of chromosome 8", "shortest_name_length": 32}
{"curie": "MONDO:0032851", "names": ["IDDILF", "intellectual developmental disorder with impaired language and dysmorphic facies", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH IMPAIRED LANGUAGE AND DYSMORPHIC FACIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder with impaired language and dysmorphic facies", "shortest_name_length": 6}
{"curie": "MONDO:0023045", "names": ["ectodermal dysplasia arthrogryposis diabetes mellitus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia arthrogryposis diabetes mellitus", "shortest_name_length": 53}
{"curie": "UMLS:C2981256", "names": ["Stage III Mucosal Melanoma of the Head and Neck", "Stage III Mucosal Melanoma of the Head and Neck AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Mucosal Melanoma of the Head and Neck AJCC v7", "shortest_name_length": 47}
{"curie": "UMLS:C0751865", "names": ["Alcohol Abuse, Nervous System", "Ethyl Alcohol Abuse Neurologic Syndromes", "Ethanol-Induced Nervous System Disorders", "Ethanol Induced Nervous System Disorders", "Ethanol-Induced Disorders, Nervous System", "Alcohol-Induced Disorders, Nervous System", "Nervous System Disorders, Ethanol Induced", "Nervous System Disorders, Ethanol-Induced", "Ethanol Induced Disorders, Nervous System", "Alcohol Induced Disorders, Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alcohol-Induced Disorders, Nervous System", "shortest_name_length": 29}
{"curie": "UMLS:C1378111", "names": ["Stage IV Pharyngeal Cancer", "Stage IV Pharynx Carcinoma", "Pharyngeal Cancer Stage IV", "Stage IV Carcinoma of Pharynx", "Stage IV Pharyngeal Carcinoma", "Stage IV Pharyngeal Throat Cancer", "Stage IV Carcinoma of the Pharynx"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Pharynx Carcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0004241", "names": ["osteochondrosis", "Osgood-Schlatter", "Schlatter-Osgood", "Morbus Osgood-Schlatter", "osgood schlatter disease", "osgood-schlatter disease", "disease osgood schlatter", "OSGOOD SCHLATTER DISEASE", "Osgood Schlatter Disease", "Osgood Schlatter disease", "Disease;Osgood-Schlatter", "Osgood-Schlatter disease", "Osgood-Schlatter Disease", "OSGOOD-SCHLATTER DISEASE", "disease osgood-schlatter", "diseases osgood schlatter", "disease osgood schlatters", "Osgood Schlatters disease", "osgood-schlatter's disease", "Osgood Schlatter's disease", "Osgood-Schlatter's Disease", "schlatter's disease osgood", "Osgood-Schlatter's disease", "disease osgoods schlatters", "osgood schlatter's disease", "disease osgoods schlatter's", "disease osgood schlatters's", "tibial tubercle osteochondrosis", "Osgood-Schlatter/osteochondroses", "osteochondrosis; Osgood-Schlatter", "Osteochondrosis of proximal tibia", "Osgood-Schlatter; osteochondrosis", "osteochondritis of tibial tubercle", "Osteochondrosis of tibial tubercle", "Osteochondritis of tibial tubercle", "Osteochondrosis of Osgood-Schlatter", "Osgood Schlatter disease (diagnosis)", "Osteochondritis of the proximal tibia", "osteochondritis of the tibial tubercle", "Osteochondrosis of the tibial tubercle", "Aseptic necrosis of the tibial tubercle", "aseptic necrosis of the tibial tubercle", "Tibial tubercle juvenile osteochondritis", "Juvenile osteochondrosis of tibia tubercle", "Juvenile osteochondrosis of tibial tubercle", "juvenile osteochondrosis of tibial tubercle", "Osteochondritis of tibial tubercle (disorder)", "Juvenile osteochondrosis of tibial tubercle (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Osgood-Schlatter disease", "shortest_name_length": 15}
{"curie": "MONDO:0010772", "names": ["LDYT", "Marsden syndrome", "MARSDEN SYNDROME", "LHON and dystonia", "LEBER OPTIC ATROPHY AND DYSTONIA", "Leber optic atrophy and dystonia", "Leber optic atrophy with dystonia", "Leber hereditary optic neuropathy and dystonia", "LEBER HEREDITARY OPTIC NEUROPATHY WITH DYSTONIA", "Leber Hereditary Optic Neuropathy With Dystonia", "Leber Hereditary optic neuropathy with dystonia", "Leber hereditary optic neuropathy with dystonia", "Leber's hereditary optic neuropathy with dystonia", "familial dystonia with visual failure and striatal lucencies", "dystonia familial, with visual failure and striatal lucencies", "dystonia, familial, with visual failure and striatal lucencies", "DYSTONIA, FAMILIAL, WITH VISUAL FAILURE AND STRIATAL LUCENCIES", "Dystonia, familial, with visual failure and striatal lucencies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leber optic atrophy and dystonia", "shortest_name_length": 4}
{"curie": "MONDO:0017058", "names": ["RI-CMT", "autosomal recessive intermediate Charcot-Marie-Tooth disease", "intermediate Charcot-Marie-Tooth disease, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive intermediate Charcot-Marie-Tooth disease", "shortest_name_length": 6}
{"curie": "UMLS:C1883352", "names": ["Tobacco Chewing Toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tobacco Chewing Toxicity", "shortest_name_length": 24}
{"curie": "MONDO:0002754", "names": ["EP", "Extraosseous plasmacytoma", "extraosseous plasmacytoma", "Extraosseous Plasmacytoma", "Extramedullary Plasmacytoma", "extramedullary plasmacytoma", "Extramedullary plasmacytoma", "plasmacytoma, extramedullary", "Plasmacytoma, extramedullary", "Extramedullary plasmacytoma NOS", "Extramedullary plasmacytoma (clinical)", "extramedullary plasmacytoma (clinical)", "extramedullary plasmacytoma (diagnosis)", "Plasmacytoma, extramedullary (not occurring in bone)", "plasmacytoma, extramedullary (not occurring in bone)", "Malignant plasma cell neoplasm, extramedullary plasmacytoma", "Malignant plasma cell neoplasm, extramedullary plasmacytoma (disorder)", "Plasmacytoma, extramedullary (not occurring in bone) (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extramedullary plasmacytoma", "shortest_name_length": 2}
{"curie": "UMLS:C4552015", "names": ["Stage IIB", "stage IIB cancer of testis", "Stage IIB Cancer of Testis", "stage IIB testicular cancer", "Stage IIB Testicular Cancer", "stage IIB cancer of the testis", "Stage IIB Cancer of the Testis", "Stage IIB Testicular Cancer AJCC v6", "stage IIB testicular cancer AJCC v6", "Stage IIB Testicular Cancer AJCC v7", "stage IIB testicular cancer AJCC v7", "Stage IIB Testicular Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Testicular Cancer AJCC v6 and v7", "shortest_name_length": 9}
{"curie": "UMLS:C0334456", "names": ["Periosteal sarcoma", "Periosteal sarcoma, NOS", "Periosteal Fibrosarcoma", "Periosteal fibrosarcoma", "Periosteal fibrosarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Periosteal fibrosarcoma", "shortest_name_length": 18}
{"curie": "UMLS:C2367458", "names": ["Recurrent Acute Undifferentiated Leukemia", "Acute Undifferentiated Leukemia in Relapse", "acute undifferentiated leukemia in relapse", "acute undifferentiated leukemia in relapse (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute undifferentiated leukemia in relapse", "shortest_name_length": 41}
{"curie": "MONDO:0014378", "names": ["CILD29", "primary ciliary dyskinesia 29", "Primary Ciliary Dyskinesia 29", "CILIARY DYSKINESIA, PRIMARY, 29", "ciliary dyskinesia, primary, 29", "CCNO primary ciliary dyskinesia", "primary ciliary dyskinesia type 29", "ciliary dyskinesia, primary, type 29", "primary ciliary dyskinesia 29 without situs inversus", "primary ciliary dyskinesia caused by mutation in CCNO", "ciliary dyskinesia, primary, 29, without situs inversus", "CILIARY DYSKINESIA, PRIMARY, 29, WITHOUT SITUS INVERSUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia 29", "shortest_name_length": 6}
{"curie": "UMLS:C4725846", "names": ["Unresectable Gastroesophageal Junction Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Gastroesophageal Junction Adenocarcinoma", "shortest_name_length": 53}
{"curie": "UMLS:C0862402", "names": ["Stage II Bladder Urothelial Cancer", "Stage II Bladder Urothelial Carcinoma", "Urothelial carcinoma bladder stage II", "Bladder transitional cell carcinoma stage II", "Stage II Bladder Urothelial Carcinoma AJCC v7", "Stage II Bladder Urothelial Carcinoma AJCC v6", "Stage II Transitional Cell Carcinoma of Bladder", "Stage II Transitional Cell Carcinoma of the Bladder", "Transitional cell carcinoma of the bladder stage II", "Stage II Bladder Urothelial Carcinoma AJCC v6 and v7", "Stage II Urinary Bladder Transitional Cell Carcinoma", "Stage II Transitional Cell Carcinoma of Urinary Bladder", "Stage II Transitional Cell Carcinoma of the Urinary Bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder transitional cell carcinoma stage II", "shortest_name_length": 34}
{"curie": "UMLS:C1273758", "names": ["Pupillary block", "Pupillary Block", "Pupillary block (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pupillary block", "shortest_name_length": 15}
{"curie": "UMLS:C4289928", "names": ["Benign Cervical Soft Tissue Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Cervical Soft Tissue Neoplasm", "shortest_name_length": 36}
{"curie": "MONDO:0017514", "names": ["split foot, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "split foot, bilateral", "shortest_name_length": 21}
{"curie": "MONDO:0013843", "names": ["meconium ileus", "GUCY2C meconium ileus", "meconium ileus caused by mutation in GUCY2C", "Meconium ileus due to guanylate cyclase 2C deficiency", "meconium ileus due to guanylate cyclase 2C deficiency", "Intestinal obstruction in newborn due to guanylate cyclase 2C deficiency", "Intestinal obstruction in the newborn due to guanylate cyclase 2C deficiency", "intestinal obstruction in the newborn due to guanylate cyclase 2C deficiency", "Intestinal obstruction in newborn due to guanylate cyclase 2C deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intestinal obstruction in the newborn due to guanylate cyclase 2C deficiency", "shortest_name_length": 14}
{"curie": "UMLS:C2984086", "names": ["Gastric Cancer by AJCC v7 Stage", "Gastric Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Cancer by AJCC v7 Stage", "shortest_name_length": 31}
{"curie": "UMLS:C4086206", "names": ["Collapsed Lumen", "COLLAPSED LUMEN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Collapsed Lumen", "shortest_name_length": 15}
{"curie": "MONDO:0006098", "names": ["ALH", "atypical lobular hyperplasia", "Atypical Breast Lobular Hyperplasia", "atypical lobular breast hyperplasia", "Atypical Lobular Breast Hyperplasia", "atypical breast lobular hyperplasia", "Breast Atypical Lobular Hyperplasia", "Atypical Lobular Hyperplasia of Breast", "atypical lobular hyperplasia of breast", "Atypical lobular hyperplasia of breast", "Atypical Lobular Hyperplasia of the Breast", "atypical lobular hyperplasia of the breast", "atypical lobular hyperplasia (ALH) of breast", "Atypical lobular hyperplasia of breast (disorder)", "atypical lobular hyperplasia (ALH) of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical lobular breast hyperplasia", "shortest_name_length": 3}
{"curie": "UMLS:C1336308", "names": ["Stage II Ovarian Embryonal Carcinoma", "Ovarian Embryonal Carcinoma, Stage II", "Stage II Ovarian Embryonal Carcinoma AJCC v6", "Stage II Ovarian Embryonal Carcinoma AJCC v7", "Stage II Ovarian Embryonal Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Ovarian Embryonal Carcinoma AJCC v6 and v7", "shortest_name_length": 36}
{"curie": "UMLS:C5420548", "names": ["Refractory AL Amyloidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory AL Amyloidosis", "shortest_name_length": 25}
{"curie": "MONDO:0014070", "names": ["OCA7", "LRMDA oculocutaneous albinism", "albinism oculocutaneous type 7", "Oculocutaneous albinism type 7", "oculocutaneous albinism type 7", "albinism, oculocutaneous, type 7", "oculocutaneous albinism type VII", "ALBINISM, OCULOCUTANEOUS, TYPE VII", "albinism, oculocutaneous, type VII", "Oculocutaneous albinism type 7 (disorder)", "oculocutaneous albinism type 7 (diagnosis)", "oculocutaneous albinism caused by mutation in LRMDA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculocutaneous albinism type 7", "shortest_name_length": 4}
{"curie": "MONDO:0016810", "names": ["arPEO", "autosomal recessive progressive external ophthalmoplegia", "Autosomal recessive progressive external ophthalmoplegia", "Progressive External Ophthalmoplegia, Autosomal Recessive", "progressive external ophthalmoplegia, autosomal recessive", "arPEO- autosomal recessive progressive external ophthalmoplegia", "Autosomal recessive progressive external ophthalmoplegia (disorder)", "Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Recessive", "PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive progressive external ophthalmoplegia", "shortest_name_length": 5}
{"curie": "MONDO:0018325", "names": ["juvenile myasthenia gravis", "pediatric myasthenia gravis", "childhood myasthenia gravis", "juvenile acquired myasthenia", "myasthenia gravis of childhood", "juvenile autoimmune myasthenia gravis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile myasthenia gravis", "shortest_name_length": 26}
{"curie": "UMLS:C4683580", "names": ["Lugano Classification Stage II Bulky Adult Non-Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage II Bulky Adult Non-Hodgkin Lymphoma AJCC v8", "shortest_name_length": 71}
{"curie": "MONDO:0012886", "names": ["IBD22", "inflammatory bowel disease 22", "Inflammatory Bowel Disease 22", "INFLAMMATORY BOWEL DISEASE 22", "inflammatory bowel disease type 22"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory bowel disease 22", "shortest_name_length": 5}
{"curie": "UMLS:C5206578", "names": ["Testicular Nasal Type Extranodal NK/T-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular Nasal Type Extranodal NK/T-Cell Lymphoma", "shortest_name_length": 51}
{"curie": "MONDO:0009597", "names": ["MDST", "metaphyseal dysplasia, Spahr type", "METAPHYSEAL DYSPLASIA, SPAHR TYPE", "Metaphyseal chondrodysplasia Spahr type", "metaphyseal chondrodysplasia Spahr type", "Spahr type metaphyseal chondrodysplasia", "Spahr type Metaphyseal chondrodysplasia", "Metaphyseal Chondrodysplasia, Spahr Type", "Metaphyseal chondrodysplasia, Spahr type", "metaphyseal chondrodysplasia, Spahr type", "METAPHYSEAL CHONDRODYSPLASIA, SPAHR TYPE", "Metaphyseal chondrodysplasia, Spahr type (disorder)", "Metaphyseal chondrodysplasia, Spahr type (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metaphyseal chondrodysplasia, Spahr type", "shortest_name_length": 4}
{"curie": "UMLS:C4551866", "names": ["Stage IB", "stage IB cancer of testis", "Stage IB Cancer of Testis", "Stage IB Testicular Cancer", "stage IB testicular cancer", "Stage IB Cancer of the Testis", "stage IB cancer of the testis", "stage IB testicular cancer AJCC v7", "Stage IB Testicular Cancer AJCC v7", "Stage IB Testicular Cancer AJCC v6", "stage IB testicular cancer AJCC v6", "Stage IB Testicular Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Testicular Cancer AJCC v6 and v7", "shortest_name_length": 8}
{"curie": "MONDO:0019788", "names": ["Non-secreting paraganglioma", "non-secreting paraganglioma", "non-functioning paraganglioma", "paraganglioma non-functioning", "Non-functioning paraganglioma", "Non-functioning paraganglioma (disorder)", "Non-functioning paraganglioma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-secreting paraganglioma", "shortest_name_length": 27}
{"curie": "MONDO:0002127", "names": ["ankylurethria", "URETHRA STENOSIS", "Stenosis;urethral", "stenosis; urethra", "urethra; stenosis", "URETHRAL STENOSIS", "Urethral stenosis", "Urethral Stenosis", "Urethral Stenoses", "urethral stenosis", "Stenoses, Urethral", "narrowing; urethra", "Urethral Stricture", "urethral stricture", "Stenosis, Urethral", "urethra; narrowing", "Stricture, Urethral", "Urethral Strictures", "Strictures, Urethral", "urethra; contracture", "Narrowing of the urethra", "Urethral Stenosis/Stricture", "urethral stricture (disease)", "Urethral stenosis (disorder)", "urethral stenosis (diagnosis)", "Other specified causes of urethral stricture"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urethral stricture", "shortest_name_length": 13}
{"curie": "MONDO:0003589", "names": ["ovary liposarcoma", "Ovarian Liposarcoma", "ovarian liposarcoma", "liposarcoma of ovary", "Liposarcoma of Ovary", "Liposarcoma of the Ovary", "liposarcoma of the ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "liposarcoma of the ovary", "shortest_name_length": 17}
{"curie": "MONDO:0009877", "names": ["Laron Syndrome", "Laron dwarfism", "Laron syndrome", "Laron-type dwarfism", "pituitary dwarfism 2", "primary GH resistance", "pituitary dwarfism II", "GH receptor deficiency", "primary GH insensitivity", "Laron type pituitary dwarfism I", "primary growth hormone resistance", "Growth hormone receptor deficiency", "Growth Hormone Receptor Deficiency", "primary growth hormone insensitivity", "growth hormone insensitivity syndrome", "complete growth hormone insensitivity", "Laron-type isolated somatotropin defect", "short stature due to growth hormone resistance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laron syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C5446411", "names": ["Lacrimal Gland Warthin Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lacrimal Gland Warthin Tumor", "shortest_name_length": 28}
{"curie": "UMLS:C1336491", "names": ["Stage I Thyroid Medullary Carcinoma", "Stage I Medullary Carcinoma of Thyroid", "Stage I Thyroid Gland Medullary Cancer", "Stage I Thyroid Gland Medullary Carcinoma", "Stage I Medullary Thyroid Gland Carcinoma", "Stage I Medullary Carcinoma of the Thyroid", "Stage I Medullary Carcinoma of Thyroid Gland", "Stage I Medullary Carcinoma of the Thyroid Gland", "Stage I Thyroid Gland Medullary Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Thyroid Gland Medullary Carcinoma AJCC v7", "shortest_name_length": 35}
{"curie": "UMLS:C1709249", "names": ["Non-Neoplastic Esophageal Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Esophageal Disorder", "shortest_name_length": 34}
{"curie": "MONDO:0020845", "names": ["PEOB5", "autosomal recessive progressive external ophthalmoplegia 5", "PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE 5", "progressive external ophthalmoplegia, autosomal recessive 5", "autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 5", "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5", "PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5", "shortest_name_length": 5}
{"curie": "MONDO:0002469", "names": ["mixed lacrimal gland cancer", "Lacrimal Gland Malignant Mixed Tumor", "lacrimal gland malignant mixed tumor", "Malignant mixed tumor of lacrimal gland", "Lacrimal Gland Malignant Mixed Neoplasm", "lacrimal gland malignant mixed neoplasm", "Malignant Mixed Tumor of Lacrimal Gland", "malignant mixed tumor of lacrimal gland", "Malignant mixed tumour of lacrimal gland", "malignant mixed neoplasm of lacrimal gland", "Malignant Mixed Neoplasm of Lacrimal Gland", "malignant mixed tumor of the lacrimal gland", "Malignant Mixed Tumor of the Lacrimal Gland", "Malignant Mixed Neoplasm of the Lacrimal Gland", "malignant mixed neoplasm of the lacrimal gland", "lacrimal gland carcinoma ex pleomorphic adenoma", "Lacrimal Gland Carcinoma ex Pleomorphic Adenoma", "carcinoma ex pleomorphic adenoma of lacrimal gland", "Carcinoma ex pleomorphic adenoma of lacrimal gland", "Carcinoma ex Pleomorphic Adenoma of Lacrimal Gland", "Carcinoma in pleomorphic adenoma of lacrimal gland", "malignant mixed tumor of lacrimal gland (diagnosis)", "carcinoma Ex Pleomorphic adenoma of the lacrimal gland", "carcinoma ex pleomorphic adenoma of the lacrimal gland", "Carcinoma ex Pleomorphic Adenoma of the Lacrimal Gland", "carcinoma Ex pleomorphic adenoma of the lacrimal gland", "Carcinoma ex pleomorphic adenoma of lacrimal gland (disorder)", "carcinoma ex pleomorphic adenoma of lacrimal gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lacrimal gland carcinoma ex pleomorphic adenoma", "shortest_name_length": 27}
{"curie": "MONDO:0011950", "names": ["SCAR6", "NORWEGIAN INFANTILE ONSET ATAXIA", "Norwegian infantile onset ataxia", "spinocerebellar ataxia autosomal recessive 6", "autosomal recessive spinocerebellar ataxia 6", "spinocerebellar ataxia, autosomal recessive 6", "Spinocerebellar ataxia, autosomal recessive 6", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 6", "autosomal recessive spinocerebellar ataxia type 6", "Autosomal recessive spinocerebellar ataxia type 6", "SCAR6 - autosomal recessive spinocerebellar ataxia type 6", "cerebellar ataxia infantile nonprogressive autosomal recessive", "cerebellar ataxia, infantile nonprogressive, autosomal recessive", "CEREBELLAR ATAXIA, INFANTILE NONPROGRESSIVE, AUTOSOMAL RECESSIVE", "Cerebellar ataxia, infantile nonprogressive, autosomal recessive", "Infantile-onset autosomal recessive nonprogressive cerebellar ataxia", "infantile-onset autosomal recessive nonprogressive cerebellar ataxia", "Infantile-onset autosomal recessive non progressive cerebellar ataxia", "Infantile-onset autosomal recessive non progressive cerebellar ataxia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile-onset autosomal recessive nonprogressive cerebellar ataxia", "shortest_name_length": 5}
{"curie": "MONDO:0022876", "names": ["Cortes Lacassie syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cortes Lacassie syndrome", "shortest_name_length": 24}
{"curie": "UMLS:C0266814", "names": ["Gastrointestinal food allergy, NOS", "Gastrointestinal food sensitivity, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal food allergy, NOS", "shortest_name_length": 34}
{"curie": "MONDO:0005976", "names": ["Lues", "lues", "Syphilis", "syphilis", "SYPHILIS", "Great Pox", "Syphilis NOS", "Syphilis, NOS", "luetic disease", "Luetic disease", "syphilitic chancre", "Syphilis (disorder)", "syphilis (diagnosis)", "Syphilis, unspecified", "Syphilis, stage unspecified", "Treponema pallidum infection", "Treponema pallidum; infection", "Infection by Treponema pallidum", "Treponema pallidum infectious disease", "Treponema pallidum disease or disorder", "Treponema pallidum caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syphilis", "shortest_name_length": 4}
{"curie": "UMLS:C4745019", "names": ["Relapsed Acute Erythroid Leukemia", "Recurrent Acute Erythroid Leukemia", "Acute erythroid leukemia, in relapse"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Acute Erythroid Leukemia", "shortest_name_length": 33}
{"curie": "UMLS:C2188069", "names": ["Laryngeal Undifferentiated Carcinoma", "undifferentiated carcinoma of larynx", "Undifferentiated Laryngeal Throat Cancer", "undifferentiated carcinoma of larynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "undifferentiated carcinoma of larynx", "shortest_name_length": 36}
{"curie": "UMLS:C5203918", "names": ["Chronic Ocular Graft Versus Host Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic Ocular Graft Versus Host Disease", "shortest_name_length": 40}
{"curie": "MONDO:0007511", "names": ["ectodermal dysplasia trichoodontoonychial type", "Ectodermal dysplasia trichoodontoonychial type", "Ectodermal Dysplasia, Trichoodontoonychial Type", "Ectodermal dysplasia, trichoodontoonychial type", "ectodermal dysplasia, trichoodontoonychial type", "ECTODERMAL DYSPLASIA, TRICHOODONTOONYCHIAL TYPE", "Ectodermal dysplasia trichoodontoonychial type (disorder)", "Ectodermal dysplasia trichoodontoonychial type (diagnosis)", "anomalies of skin ectodermal dysplasia trichoodontoonychial type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia, trichoodontoonychial type", "shortest_name_length": 46}
{"curie": "UMLS:C0021564", "names": ["Insect Bite", "INSECT BITE", "Insect bite", "insect bite", "Bite;insect", "bite; insect", "Insect Bites", "Bite, Insect", "INSECT BITES", "insect bites", "insect; bite", "Bites, Insect", "Insect bite NOS", "BITE WOUND INSECT", "Insect bite - wound", "insect bite (diagnosis)", "Insect bite - wound (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Insect Bites", "shortest_name_length": 11}
{"curie": "MONDO:0009237", "names": ["FEH, oral", "FEH, ORAL", "heck disease", "Heck disease", "HECK DISEASE", "Heck Disease", "Hecks Disease", "Disease, Heck", "Heck's disease", "heck's disease", "Heck's Disease", "Disease, Heck's", "focal epithelial hyperplasia", "Focal Epithelial Hyperplasia", "Focal epithelial hyperplasia", "Focal Epithelial Hyperplasias", "Epithelial Hyperplasia, Focal", "Hyperplasia, Focal Epithelial", "Epithelial Hyperplasias, Focal", "Hyperplasias, Focal Epithelial", "Multifocal epithelial hyperplasia", "Oral focal epithelial hyperplasia", "multifocal epithelial hyperplasia", "FOCAL EPITHELIAL HYPERPLASIA, ORAL", "Focal Epithelial Hyperplasia, Oral", "focal epithelial hyperplasia, oral", "Focal epithelial hyperplasia of mouth", "focal epithelial hyperplasia of mouth", "Focal epithelial hyperplasia of mouth (disorder)", "focal epithelial hyperplasia of mouth (diagnosis)", "Focal epithelial hyperplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal epithelial hyperplasia", "shortest_name_length": 9}
{"curie": "MONDO:0022862", "names": ["cormier rustin munnich syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cormier rustin munnich syndrome", "shortest_name_length": 31}
{"curie": "UMLS:C4727985", "names": ["Ewing-Like Sarcoma", "Ewing-like sarcoma", "Round Cell Sarcoma with EWSR1-non-ETS Fusion", "Round cell sarcoma with EWSR1-non-ETS fusions", "Round Cell Sarcoma with EWSR1::non-ETS Fusion", "Round cell sarcoma with EWSR1-non-ETS fusions (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Round cell sarcoma with EWSR1-non-ETS fusions", "shortest_name_length": 18}
{"curie": "UMLS:C0343263", "names": ["chondrolysis", "Chondrolysis", "chondrolysis (diagnosis)", "Chondrolysis of articular cartilage", "Chondrolysis of articular cartilage (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chondrolysis of articular cartilage", "shortest_name_length": 12}
{"curie": "UMLS:C5418890", "names": ["Metastatic Ovarian Endometrioid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Ovarian Endometrioid Adenocarcinoma", "shortest_name_length": 46}
{"curie": "MONDO:0017385", "names": ["MPSI", "MPEI", "MMPEI", "MMPSI", "migrating partial seizures of infancy", "migrating partial epilepsy of infancy", "Migrating partial epilepsy of infancy", "migrating Partial seizures in infancy", "Migrating partial seizures of infancy", "Migrating partial seizures in infancy", "Migrating Partial Seizures in Infancy", "Malignant migrating focal seizures of infancy", "malignant migrating Partial seizures in infancy", "malignant migrating partial epilepsy of infancy", "malignant migrating partial seizures of infancy", "Malignant migrating partial seizures of infancy", "Malignant migrating partial epilepsy of infancy", "Malignant Migrating Partial Seizures in Infancy", "Migrating partial seizures in infancy (disorder)", "Epilepsy of infancy with migrating focal seizures", "MMPSI - malignant migrating partial seizures of infancy", "Malignant migrating partial seizures of infancy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant migrating partial seizures of infancy", "shortest_name_length": 4}
{"curie": "UMLS:C1335899", "names": ["Salivary Gland Ductal Papilloma", "ductal papilloma of salivary gland", "ductal papilloma of salivary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ductal papilloma of salivary gland", "shortest_name_length": 31}
{"curie": "UMLS:C4331338", "names": ["Stage IVA Major Salivary Gland Cancer", "Stage IVA Major Salivary Gland Cancer AJCC v8", "Stage IVA Major Salivary Gland Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Major Salivary Gland Cancer AJCC v8", "shortest_name_length": 37}
{"curie": "UMLS:C5557175", "names": ["Stage IIIA Cervical Cancer AJCC v9", "Stage IIIA Cervical Carcinoma AJCC v9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Cervical Cancer AJCC v9", "shortest_name_length": 34}
{"curie": "UMLS:C0267003", "names": ["oral abscess", "ORAL ABSCESS", "Abscess oral", "mouth abscess", "Mouth abscess", "abscess mouth", "abscesses oral", "mouth; abscess", "abscesses mouth", "Abscess of mouth", "of mouth abscess", "Abscess of mouth, NOS", "Abscess of oral tissue", "Abscess of oral tissue, NOS", "Abscess of oral soft tissue", "Abscess of oral tissue (disorder)", "Abscess of oral tissue (diagnosis)", "Abscess of oral soft tissue (disorder)", "Abscess of oral soft tissue (diagnosis)", "disorder of mouth abscess of oral tissue", "disorder of mouth abscess of oral soft tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abscess of oral soft tissue", "shortest_name_length": 12}
{"curie": "MONDO:0019044", "names": ["tumor of hematopoietic and lymphoid tissues"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tumor of hematopoietic and lymphoid tissues", "shortest_name_length": 43}
{"curie": "MONDO:0014860", "names": ["PCLD2", "polycystic liver disease 2", "polycystic liver disease type 2", "polycystic liver disease 2; PCLD2", "POLYCYSTIC LIVER DISEASE 2 WITH OR WITHOUT KIDNEY CYSTS", "polycystic liver disease 2 with or without kidney cysts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polycystic liver disease 2", "shortest_name_length": 5}
{"curie": "MONDO:0100310", "names": ["ataxia; Marie", "Marie; ataxia", "Marie's ataxia", "marie's ataxia", "Nonne-Marie syndrome", "Marie cerebellar ataxia", "Marie Cerebellar Ataxia", "Marie; cerebellar ataxia", "cerebellar ataxia; Marie", "Cerebellar Ataxia, Marie", "Marie's Cerebellar Ataxia", "Marie's cerebellar ataxia", "Familial cerebellar ataxia", "Cerebellar Ataxia, Marie's", "Cerebellar ataxia, Marie's", "familial cerebellar ataxia", "cerebellar hereditary ataxia", "Hereditary cerebellar ataxia", "hereditary cerebellar ataxia", "Hereditary Cerebellar Ataxia", "Hereditary cerebellar ataxia NOS", "Marie's cerebellar ataxia (disorder)", "Marie's cerebellar ataxia (diagnosis)", "ataxia; cerebellar, late onset (Marie)", "cerebellar; ataxia, late onset (Marie)", "Familial cerebellar degeneration syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary cerebellar ataxia", "shortest_name_length": 13}
{"curie": "UMLS:C0273112", "names": ["Contusio Cordis", "contusion heart", "heart contusion", "Heart Contusion", "Contusion, Heart", "Cordis, Contusio", "contusions heart", "Heart Contusions", "Cardiac contusion", "CARDIAC CONTUSION", "Cardiac Contusion", "cardiac contusion", "Contusions, Heart", "cardiac contusions", "Contusion to heart", "Cardiac Contusions", "Contusion, Cardiac", "Contusion of heart", "Contusions, Cardiac", "Myocardial contusion", "myocardial contusion", "Myocardial Contusion", "Myocardial Contusions", "Contusion, Myocardial", "Contusions, Myocardial", "Contusion to heart (disorder)", "myocardial contusion (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myocardial Contusions", "shortest_name_length": 15}
{"curie": "UMLS:C4745017", "names": ["Relapsed Acute Myeloid Leukemia with Multilineage Dysplasia", "Recurrent Acute Myeloid Leukemia with Multilineage Dysplasia", "Acute myeloid leukemia with multilineage dysplasia, in relapse", "Recurrent Acute Myeloid Leukemia (AML) with Multilineage Dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Acute Myeloid Leukemia with Multilineage Dysplasia", "shortest_name_length": 59}
{"curie": "MONDO:0005149", "names": ["pulmonary hypertension", "Hypertension, Pulmonary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary hypertension", "shortest_name_length": 22}
{"curie": "MONDO:0014443", "names": ["BBS15", "Bardet-Biedl syndrome 15", "BARDET-BIEDL SYNDROME 15", "WDPCP Bardet-Biedl syndrome", "Bardet-Biedl syndrome type 15", "Bardet-Biedl syndrome caused by mutation in WDPCP"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bardet-Biedl syndrome 15", "shortest_name_length": 5}
{"curie": "MONDO:0012840", "names": ["IBD17", "INFLAMMATORY BOWEL DISEASE 17", "inflammatory bowel disease 17", "Inflammatory Bowel Disease 17", "IL23R inflammatory bowel disease", "inflammatory bowel disease type 17", "inflammatory bowel disease 17, protection against", "inflammatory bowel disease caused by mutation in IL23R"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory bowel disease 17", "shortest_name_length": 5}
{"curie": "UMLS:C1332940", "names": ["Childhood Acute Lymphoid Leukemia in Partial Remission", "Pediatric Acute Lymphoid Leukemia in Partial Remission", "Acute Lymphoblastic Leukemia (ALL) in Partial Remission", "Childhood Acute Lymphocytic Leukemia in Partial Remission", "Pediatric Acute Lymphocytic Leukemia in Partial Remission", "Childhood Acute Lymphogenous Leukemia in Partial Remission", "Pediatric Acute Lymphogenous Leukemia in Partial Remission", "Childhood Acute Lymphoblastic Leukemia in Partial Remission", "Pediatric Acute Lymphoblastic Leukemia in Partial Remission", "Childhood Precursor Lymphoblastic Leukemia in Partial Remission"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Acute Lymphoblastic Leukemia in Partial Remission", "shortest_name_length": 54}
{"curie": "MONDO:0018051", "names": ["Jessner disease", "Jessner-Kanof syndrome", "benign lymphocytic infiltration", "Jessners lymphocytic infiltrate", "Jessner's lymphocytic infiltrate", "lymphocytic infiltrate of Jessner", "Jessner's lymphocytic infiltration", "Lymphocytic infiltration of Jessner-Kanof", "Benign lymphocytic infiltration of Jessner", "Jessner's lymphocytic infiltration of skin", "benign chronic T-cell infiltrative disorder", "Jessner lymphocytic infiltration of the skin", "Jessner-Kanof lymphocytic infiltration of the skin", "Benign lymphocytic infiltration of Jessner (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jessner lymphocytic infiltration of the skin", "shortest_name_length": 15}
{"curie": "MONDO:0009382", "names": ["PSHB", "hyperbilirubinemia, shunt, primary", "HYPERBILIRUBINEMIA, SHUNT, PRIMARY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperbilirubinemia, shunt, primary", "shortest_name_length": 4}
{"curie": "UMLS:C2828186", "names": ["Stage IIA Gestational Trophoblastic Tumor", "Stage IIA Gestational Trophoblastic Tumor AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Gestational Trophoblastic Tumor AJCC v7", "shortest_name_length": 41}
{"curie": "MONDO:0020067", "names": ["Brain inflammation", "Encephalitis infection", "encephalitis infection", "Infective encephalitis", "Infectious encephalitis", "infectious encephalitis", "Infectious Encephalitis", "Encephalitis, Infectious", "encephalitis; infectious", "infectious; encephalitis", "Infective encephalitis (disorder)", "infectious; encephalitis (etiology)", "infectious; encephalitis (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infectious encephalitis", "shortest_name_length": 18}
{"curie": "MONDO:0003841", "names": ["Heart Lipoma", "heart lipoma", "Cardiac lipoma", "Cardiac Lipoma", "cardiac lipoma", "lipoma of heart", "Lipoma of Heart", "Lipoma of the Heart", "lipoma of the heart", "benign lipoma of heart", "benign lipoma of heart (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heart lipoma", "shortest_name_length": 12}
{"curie": "MONDO:0018696", "names": ["corticobasal syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corticobasal syndrome", "shortest_name_length": 21}
{"curie": "MONDO:0008139", "names": ["OSLAM syndrome", "Oslam syndrome", "OSLAM SYNDROME", "OSTEOSARCOMA, LIMB ANOMALIES, AND MACROCYTOSIS", "osteosarcoma, limb anomalies, and macrocytosis", "Osteosarcoma-limb anomalies-erythroid macrocytosis syndrome", "osteosarcoma-limb anomalies-erythroid macrocytosis syndrome", "Osteosarcoma, limb anomalies, erythroid macrocytosis syndrome", "OSLAM (osteosarcoma, limb anomalies, erythroid macrocytosis) syndrome", "Osteosarcoma, limb anomalies, erythroid macrocytosis syndrome (disorder)", "osteosarcoma, limb anomalies, and erythroid macrocytosis with megaloblastic marrow", "OSTEOSARCOMA, LIMB ANOMALIES, AND ERYTHROID MACROCYTOSIS WITH MEGALOBLASTIC MARROW", "osteosarcoma, limb anomalies (clinodactyly, absence of digital ray in foot, bilateral radioulnar synostosis) and macrocytosis without anemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "OSLAM syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C5669720", "names": ["Transformed Lymphoplasmacytic Lymphoma to Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transformed Lymphoplasmacytic Lymphoma to Diffuse Large B-Cell Lymphoma", "shortest_name_length": 71}
{"curie": "UMLS:C0029230", "names": ["ORGANIC MENTAL DISORDER PSYCHOTIC", "Organic Mental Disorders, Psychotic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Organic Mental Disorders, Psychotic", "shortest_name_length": 33}
{"curie": "MONDO:0018796", "names": ["isolated constitutional thrombocytopenia", "non-syndromic constitutional thrombocytopenia", "Cconstitutional thrombocytopenia without extra-hematopoietic manifestation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated constitutional thrombocytopenia", "shortest_name_length": 40}
{"curie": "MONDO:0009679", "names": ["arthrogryposis due to muscular dystrophy", "congenital muscular dystrophy producing arthrogryposis", "muscular dystrophy, congenital, producing arthrogryposis", "Muscular Dystrophy, Congenital, Producing Arthrogryposis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis due to muscular dystrophy", "shortest_name_length": 40}
{"curie": "MONDO:0019402", "names": ["Cooley anemia", "B-thalassemia", "Cooley's anemia", "beta Thalassemia", "beta thalassemia", "thalassemia beta", "beta-Thalassemia", "Beta-thalassemia", "BETA-THALASSEMIA", "beta-thalassemia", "Beta thalassemia", "Thalassemia beta", "Beta Thalassemia", "THALASSEMIA BETA", "thalassaemia beta", "Beta-thalassaemia", "beta thalassemias", "beta Thalassemias", "Thalassemia, beta", "Beta thalassaemia", "beta-thalassaemia", "thalassemia; beta", "beta; thalassemia", "beta thalassaemia", "Thalassaemia beta", "Thalassemia Major", "thalassemia major", "Thalassemias, beta", "Thalassemias, beta-", "erythroblastic anemia", "beta Type Thalassemia", "beta Thalassemia, NOS", "Type Thalassemia, beta", "Thalassemia, beta Type", "Beta thalassemia minor", "beta Type Thalassemias", "beta Type Microcytemia", "Type Microcytemia, beta", "Microcytemia, beta Type", "Thalassemias, beta Type", "Type Thalassemias, beta", "beta Type Microcytemias", "Microcytemias, beta Type", "Type Microcytemias, beta", "Beta thalassemia syndrome", "Beta thalassaemia syndrome", "Beta thalassemia (disorder)", "Beta thalassemia intermedia", "beta-thalassemia (diagnosis)", "thalassemia, Hispanic gamma-delta-beta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "beta thalassemia", "shortest_name_length": 13}
{"curie": "MONDO:0015644", "names": ["audiogenic seizure", "audiogenic epilepsy", "audiogenic seizures", "Audiogenic seizures", "Audiogenic Seizures", "Audiogenic Epilepsy", "Audiogenic epilepsy", "Epilepsy, Audiogenic", "Audiogenic Epilepsies", "epilepsy reflex audiogenic", "Audiogenic Reflex Epilepsy", "Epilepsy, Audiogenic Reflex", "Reflex Epilepsy, Audiogenic", "Audiogenic Reflex Epilepsies", "Epilepsies, Audiogenic Reflex", "Reflex Epilepsies, Audiogenic", "Audiogenic epilepsy (disorder)", "Audiogenic epilepsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "audiogenic seizures", "shortest_name_length": 18}
{"curie": "MONDO:0003697", "names": ["penis non-invasive verrucous carcinoma", "non-invasive penile verrucous carcinoma", "Non-Invasive Penile Verrucous Carcinoma", "Non-Invasive Penile verrucous carcinoma", "Non-Invasive Verrucous Carcinoma of Penis", "non-invasive verrucous carcinoma of penis", "Non-Invasive Verrucous Carcinoma of the Penis", "non-invasive verrucous carcinoma of the penis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-invasive verrucous carcinoma of the penis", "shortest_name_length": 38}
{"curie": "UMLS:C0856015", "names": ["MALT Type Extranodal Marginal Zone B-Cell Lymphoma Stage IV", "Stage IV Extranodal Marginal Zone B-Cell Lymphoma (MALT Type)", "Extranodal marginal zone B-cell lymphoma (MALT type) stage IV", "Extranodal Marginal Zone B-Cell Lymphoma (MALT Type) Stage IV", "Stage IV Extranodal Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue", "Stage IV Extranodal Marginal Zone B-Cell Lymphoma of Mucosa-Associated Lymphoid Tissue", "Ann Arbor Stage IV Extranodal Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extranodal marginal zone B-cell lymphoma (MALT type) stage IV", "shortest_name_length": 59}
{"curie": "MONDO:0007546", "names": ["EMP", "MPE", "Malignant eosinophil proliferation", "Eosinophils, Malignant Proliferation of", "eosinophils, malignant proliferation of", "EOSINOPHILS, MALIGNANT PROLIFERATION OF", "myeloproliferative disorder with eosinophilia", "chronic myeloproliferative disorder with eosinophilia", "Myeloproliferative Disorder, Chronic, with Eosinophilia", "myeloproliferative disorder, chronic, with eosinophilia", "MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myeloproliferative disorder, chronic, with eosinophilia", "shortest_name_length": 3}
{"curie": "UMLS:C4288754", "names": ["Metastatic Urothelial Cancer", "Metastatic Urothelial Carcinoma", "Metastatic urothelial carcinoma", "Metastatic urothelial carcinoma (disorder)", "Metastatic urothelial carcinoma (diagnosis)", "Metastatic Transitional Cell Carcinoma of the Urinary Tract", "Metastatic transitional cell carcinoma of the urinary tract", "malignant neoplasm carcinoma transitional cell metastatic urothelial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic urothelial carcinoma", "shortest_name_length": 28}
{"curie": "UMLS:C1518698", "names": ["Ovarian Dermoid Cyst with Corticotropin Secreting Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Dermoid Cyst with Corticotropin Secreting Adenoma", "shortest_name_length": 57}
{"curie": "MONDO:0008658", "names": ["VIRUS RD114 RNA COMPLEMENTARITY", "virus Rd114 RNA Complementarity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "virus Rd114 RNA Complementarity", "shortest_name_length": 31}
{"curie": "UMLS:C0017657", "names": ["glomerulitis", "GLOMERULITIS", "Glomerulitis", "Glomerulitis NOS", "Glomerulitis, NOS", "Glomerulitis (disorder)", "glomerulitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Glomerulitis (disorder)", "shortest_name_length": 12}
{"curie": "UMLS:C2984097", "names": ["Prostate Cancer by AJCC v7 Stage", "Prostate Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Cancer by AJCC v7 Stage", "shortest_name_length": 32}
{"curie": "UMLS:C4743571", "names": ["Silent Corticotroph Adenoma", "Nonfunctional Corticotroph Adenoma", "Nonfunctioning Corticotroph Adenoma", "Non-Functioning Corticotroph Pituitary Neuroendocrine Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Functioning Corticotroph Pituitary Neuroendocrine Tumor", "shortest_name_length": 27}
{"curie": "UMLS:C0404533", "names": ["Reduced perineum", "Deficient perineum", "DECREASED ANOGENITAL DISTANCE", "Decreased anogenital distance", "Anogenital Distance Decreased", "Decreased anogenital distance (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Decreased anogenital distance", "shortest_name_length": 16}
{"curie": "MONDO:0014251", "names": ["melioidosis, resistance to", "MELIOIDOSIS, RESISTANCE TO", "susceptibility to melioidosis", "MELIOIDOSIS, SUSCEPTIBILITY TO", "melioidosis, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melioidosis, susceptibility to", "shortest_name_length": 26}
{"curie": "MONDO:0032878", "names": ["NEDBASH", "neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia", "NEURODEVELOPMENTAL DISORDER WITH BEHAVIORAL ABNORMALITIES, ABSENT SPEECH, AND HYPOTONIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia", "shortest_name_length": 7}
{"curie": "MONDO:0030606", "names": ["BRYLIB1", "Bryant-Li-Bhoj neurodevelopmental syndrome 1", "BRYANT-LI-BHOJ NEURODEVELOPMENTAL SYNDROME 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bryant-Li-Bhoj neurodevelopmental syndrome 1", "shortest_name_length": 7}
{"curie": "MONDO:0016939", "names": ["Trisomy 2p", "trisomy 2p", "2p trisomy", "2p+ syndrome", "2p duplication", "Duplication 2p", "dup(2p) syndrome", "partial trisomy 2p", "chromosome 2p trisomy", "2p duplication syndrome", "duplication 2p syndrome", "Chromosome 2, trisomy 2p", "chromosome 2p duplication", "partial trisomy of chromosome 2p", "chromosome 2p duplication syndrome", "partial duplication of chromosome 2p", "partial duplication of the short arm of chromosome 2", "partial duplication of the short arm of chromosome type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of the short arm of chromosome 2", "shortest_name_length": 10}
{"curie": "UMLS:C0332798", "names": ["wound open", "Open wound", "open wound", "WOUND OPEN", "open wounds", "OPEN WOUNDS", "Open wounds", "Open wound (disorder)", "open wound (diagnosis)", "Open wound of body region", "open wound (physical finding)", "Open wound (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Open wound", "shortest_name_length": 10}
{"curie": "MONDO:0013486", "names": ["SCA32", "SPINOCEREBELLAR ATAXIA 32", "spinocerebellar ataxia 32", "spinocerebellar ataxia type 32", "Spinocerebellar ataxia type 32", "Spinocerebellar ataxia type 32 (disorder)", "cerebellar ataxia with azoospermia and intellectual disability", "Cerebellar ataxia with azoospermia and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia type 32", "shortest_name_length": 5}
{"curie": "UMLS:C0854842", "names": ["Angioimmunoblastic T-cell lymphoma stage IV", "Angioimmunoblastic T-Cell Lymphoma Stage IV", "Stage IV Angioimmunoblastic T-Cell Lymphoma", "Ann Arbor Stage IV Angioimmunoblastic T-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Angioimmunoblastic T-cell lymphoma stage IV", "shortest_name_length": 43}
{"curie": "UMLS:C5204344", "names": ["Borderline Ovarian Mucinous Tumor/Atypical Proliferative Ovarian Mucinous Tumor with Intraepithelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Ovarian Mucinous Tumor/Atypical Proliferative Ovarian Mucinous Tumor with Intraepithelial Carcinoma", "shortest_name_length": 110}
{"curie": "MONDO:0010082", "names": ["ONAT SYNDROME", "Onat syndrome", "Fryns-van den Berghe syndrome", "Subaortic stenosis short stature syndrome", "subaortic stenosis short stature syndrome", "Subaortic stenosis-short stature syndrome", "subaortic stenosis-short stature syndrome", "Subaortic Stenosis--Short Stature Syndrome", "SUBAORTIC STENOSIS--SHORT STATURE SYNDROME", "subaortic stenosis--short stature syndrome", "Subaortic stenosis and short stature syndrome", "Subaortic stenosis and short stature syndrome (disorder)", "Peters anomaly-corneal clouding-growth and mental retardation syndrome", "aortic stenosis-corneal clouding-growth and mental retardation syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subaortic stenosis-short stature syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0011614", "names": ["HMGCS2D", "HMGCS2 DEFICIENCY", "HMGCS2 Deficiency", "Hmgcs2 deficiency", "HMG-CoA synthase deficiency", "HMG-CoA synthase 2 deficiency", "HMG CoA synthetase deficiency", "HMG-CoA synthase-2 deficiency", "HMG-coenzyme A synthase deficiency", "MITOCHONDRIAL HMG-CoA SYNTHASE DEFICIENCY", "Mitochondrial HMG-CoA Synthase Deficiency", "mitochondrial HMG-Coa synthase deficiency", "3-hydroxy-3-methylglutaryl-CoA synthase deficiency", "3-HYDROXY-3-METHYLGLUTARYL-CoA SYNTHASE-2 DEFICIENCY", "3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency", "3-hydroxy-3-methylglutaryl-CoA synthase-2 deficiency", "3-hydroxy-3-methylglutaryl-coenzyme A synthase deficiency", "Deficiency of 3-hydroxy-3-methylglutaryl-coenzyme A synthase", "Deficiency of 3-hydroxy-3-methylglutaryl-coenzyme A synthase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "3-hydroxy-3-methylglutaryl-CoA synthase deficiency", "shortest_name_length": 7}
{"curie": "MONDO:0009388", "names": ["Hyperlysinemia", "hyperlysinemia", "Hyperlysinaemia", "Hyperlysinemias", "hyperlysinemias", "LYSINE INTOLERANCE", "lysine intolerance", "Hyperlysinemia, NOS", "Hyperlysinaemia, NOS", "hyperlysinemia type I", "Hyperlysinemia type I", "Elevated blood lysine", "hyperlysinemia, type 1", "hyperlysinemia, type I", "HYPERLYSINEMIA, TYPE I", "Hyperlysinemia, type I", "Familial Hyperlysinemia", "Familial Hyperlysinemias", "hyperlysinemia (disease)", "Hyperlysinemia, Familial", "Hyperlysinemias, Familial", "Hyperlysinemia (disorder)", "hyperlysinemia (diagnosis)", "L Lysine:NAD Oxido Reductase Deficiency", "L-lysine:NAD-oxido-reductase deficiency", "L-LYSINE:NAD-OXIDO-REDUCTASE DEFICIENCY", "L-Lysine:NAD-Oxido-Reductase Deficiency", "L-lysine NAD-oxido-reductase deficiency", "Deficiency, L-Lysine:NAD-Oxido-Reductase", "L-Lysine:NAD-Oxido-Reductase Deficiencies", "Alpha-aminoadipic semialdehyde deficiency", "Deficiencies, L-Lysine:NAD-Oxido-Reductase", "Lysine alpha-ketoglutarate reductase deficiency", "Lysine:Alpha Ketoglutarate Reductase Deficiency", "lysine alpha-ketoglutarate reductase deficiency", "Lysine:Alpha-Ketoglutarate Reductase Deficiency", "LYSINE:ALPHA-KETOGLUTARATE REDUCTASE DEFICIENCY", "lysine:Alpha-ketoglutarate reductase deficiency", "Reductase Deficiency, Lysine:Alpha-Ketoglutarate", "Deficiency, Lysine:Alpha-Ketoglutarate Reductase", "Alpha Aminoadipic Semialdehyde Deficiency Disease", "Lysine:Alpha-Ketoglutarate Reductase Deficiencies", "Alpha-Aminoadipic Semialdehyde Deficiency Disease", "Deficiency Disease, Alpha-Aminoadipic Semialdehyde", "ALPHA-AMINOADIPIC SEMIALDEHYDE SYNTHASE DEFICIENCY", "Deficiency Disease, Alpha Aminoadipic Semialdehyde", "Alpha-aminoadipic semialdehyde synthase deficiency", "Reductase Deficiencies, Lysine:Alpha-Ketoglutarate", "Deficiencies, Lysine:Alpha-Ketoglutarate Reductase"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperlysinemia", "shortest_name_length": 14}
{"curie": "MONDO:0030978", "names": ["MLEHF", "ENDOVESL", "endove syndrome, limb-only type", "ENDOVE SYNDROME, LIMB-ONLY TYPE", "Mesomelia of Lower Extremities With Hand and Foot Anomalies", "MESOMELIA OF LOWER EXTREMITIES WITH HAND AND FOOT ANOMALIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endove syndrome, limb-only type", "shortest_name_length": 5}
{"curie": "MONDO:0018192", "names": ["adenocarcinoma of paratestis", "paratesticular adenocarcinoma", "adenocarcinoma of the paratestis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paratesticular adenocarcinoma", "shortest_name_length": 28}
{"curie": "UMLS:C4329259", "names": ["Acquired Hyperthyroidism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired Hyperthyroidism", "shortest_name_length": 24}
{"curie": "MONDO:0014034", "names": ["GAND", "MRD18", "GAND SYNDROME", "GAND syndrome", "autosomal dominant mental retardation 18", "mental retardation, autosomal dominant 18", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 18", "autosomal dominant intellectual disability 18", "mental retardation, autosomal dominant type 18", "intellectual disability, autosomal dominant 18", "GATAD2B-associated neurodevelopmental disorder", "intellectual disability, autosomal dominant type 18", "autosomal dominant intellectual developmental disorder 18", "autosomal dominant non-syndromic intellectual disability 18", "severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C1168175", "names": ["Incision site hematoma", "Incision site haematoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Incision site hematoma", "shortest_name_length": 22}
{"curie": "MONDO:0032697", "names": ["NEDLBA", "NEURODEVELOPMENTAL DISORDER AND LANGUAGE DELAY WITH OR WITHOUT STRUCTURAL BRAIN ABNORMALITIES", "neurodevelopmental disorder and language delay with or without structural brain abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder and language delay with or without structural brain abnormalities", "shortest_name_length": 6}
{"curie": "MONDO:0024861", "names": ["Mixed teratoma and seminoma", "mixed teratoma and seminoma", "Mixed Teratoma and Seminoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed teratoma and seminoma", "shortest_name_length": 27}
{"curie": "UMLS:C5420547", "names": ["Recurrent AL Amyloidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent AL Amyloidosis", "shortest_name_length": 24}
{"curie": "MONDO:0033542", "names": ["IMD70", "immunodeficiency 70", "IMMUNODEFICIENCY 70"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 70", "shortest_name_length": 5}
{"curie": "MONDO:0009880", "names": ["CPHD4", "pituitary hormone deficiency, combined 4", "Pituitary Hormone Deficiency, Combined, 4", "pituitary hormone deficiency, combined, 4", "PITUITARY HORMONE DEFICIENCY, COMBINED, 4", "pituitary hormone deficiency, combined, type 4", "short stature, pituitary and cerebellar defects and small sella turcica", "SHORT STATURE, PITUITARY AND CEREBELLAR DEFECTS, AND SMALL SELLA TURCICA", "Short Stature, Pituitary And Cerebellar Defects, And Small Sella Turcica", "short stature, pituitary and cerebellar defects, and small sella turcica", "pituitary hormone deficiency, combined with or without cerebellar defects", "PITUITARY HORMONE DEFICIENCY, COMBINED, WITH OR WITHOUT CEREBELLAR DEFECTS", "Pituitary Hormone Deficiency, Combined, With Or Without Cerebellar Defects", "pituitary hormone deficiency, combined, with or without cerebellar defects", "short stature-pituitary and cerebellar defects-small sella turcica syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short stature-pituitary and cerebellar defects-small sella turcica syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0012095", "names": ["intellectual disability-brachydactyly-Pierre Robin syndrome", "Robin Sequence with Distinctive Facial Appearance and Brachydactyly", "ROBIN sequence with distinctive facial appearance and brachydactyly", "ROBIN SEQUENCE WITH DISTINCTIVE FACIAL APPEARANCE AND BRACHYDACTYLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability-brachydactyly-Pierre Robin syndrome", "shortest_name_length": 59}
{"curie": "UMLS:C4763776", "names": ["Unresectable Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Lymphoma", "shortest_name_length": 21}
{"curie": "UMLS:C4763547", "names": ["Unresectable Skin Basal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Skin Basal Cell Carcinoma", "shortest_name_length": 38}
{"curie": "UMLS:C0860160", "names": ["Diabetes mellitus loss of control", "Diabetes mellitus inadequate control"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diabetes mellitus inadequate control", "shortest_name_length": 33}
{"curie": "UMLS:C1336110", "names": ["Stage IA2 Cervical Cancer", "Cervical Cancer Stage IA2", "AJCC Stage IA2 Cervical Cancer", "FIGO Stage IA2 Cervix Carcinoma", "FIGO Stage IA2 Cervical Carcinoma", "Stage IA2 Cervical Cancer AJCC v7", "FIGO Stage IA2 Carcinoma of Cervix", "FIGO Stage IA2 Cervix Uteri Carcinoma", "FIGO Stage IA2 Carcinoma of the Cervix", "FIGO Stage IA2 Uterine Cervix Carcinoma", "Stage IA2 Cervical Cancer AJCC v6 and v7", "FIGO Stage IA2 Carcinoma of Cervix Uteri", "FIGO Stage IA2 Carcinoma of Uterine Cervix", "FIGO Stage IA2 Carcinoma of the Cervix Uteri", "FIGO Stage IA2 Carcinoma of the Uterine Cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA2 Cervical Cancer", "shortest_name_length": 25}
{"curie": "MONDO:0005497", "names": ["Bone dysplasia", "bone dysplasia", "Bone Dysplasia", "Bone Dysplasias", "Dysplasia, Bone", "bone dysplasias", "dysplasias bone", "Dysplasias, Bone", "Abnormal bone growth", "Bone growth abnormal", "bone development disease", "Bone Development Disorder", "Bone development disorder", "bone development disorder", "BONE DEVELOPMENT DISORDER", "Developmental Bone Disease", "disease of bone development", "Developmental Bone Diseases", "Bone Disease, Developmental", "Disorder of bone development", "disorder of bone development", "Bone Diseases, Developmental", "bone development disease or disorder", "Disorder of bone development (disorder)", "disease or disorder of bone development"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bone development disease", "shortest_name_length": 14}
{"curie": "MONDO:0001033", "names": ["Fungal corneal ulcer", "fungal corneal ulcer", "Mycotic corneal ulcer", "mycotic corneal ulcer", "Mycotic corneal ulcer (disorder)", "mycotic corneal ulcer (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mycotic corneal ulcer", "shortest_name_length": 20}
{"curie": "UMLS:C2721738", "names": ["High Grade VAIN", "High Grade Vaginal Intraepithelial Neoplasia", "High-Grade Vaginal Squamous Intraepithelial Lesion", "Vaginal high grade squamous intraepithelial lesion", "High Grade Vaginal Squamous Intraepithelial Lesion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal high grade squamous intraepithelial lesion", "shortest_name_length": 15}
{"curie": "MONDO:0004448", "names": ["Frontal Sinus Inverted Papilloma", "frontal sinus inverted papilloma", "Inverted Papilloma of Frontal Sinus", "inverted papilloma of frontal sinus", "Inverted papilloma of the Frontal sinus", "inverted papilloma of the frontal sinus", "Inverted Papilloma of the Frontal Sinus", "Frontal Sinus Inverted Schneiderian Papilloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontal sinus inverted papilloma", "shortest_name_length": 32}
{"curie": "MONDO:0001054", "names": ["PTERYGIUM DOUBLE", "double pterygium", "Double pterygium", "Double pterygium (disorder)", "double pterygium (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "double pterygium", "shortest_name_length": 16}
{"curie": "MONDO:0004941", "names": ["EMS", "L-tryptophan induced EMS", "Eosinophilia-Myalgia Syndrome", "eosinophilia-myalgia syndrome", "Eosinophilia myalgia syndrome", "eosinophilia myalgia syndrome", "Eosinophilia Myalgia Syndrome", "EOSINOPHILIA-MYALGIA SYNDROME", "Eosinophilia-myalgia syndrome", "eosinophilia; myalgia syndrome", "Eosinophilia-Myalgia Syndromes", "syndrome; eosinophilia-myalgia", "Syndrome, Eosinophilia-Myalgia", "Syndromes, Eosinophilia-Myalgia", "EMS - Eosinophilia myalgia syndrome", "Eosinophilia myalgia syndrome (disorder)", "eosinophilia-myalgia syndrome (diagnosis)", "severe muscle pain and abnormally high eosinophils", "syndrome with inflammatory and autoimmune components that affect the skin, fascia, muscle, nerve, blood vessels, lung, and heart"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eosinophilia-myalgia syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C3897348", "names": ["Transient Myocardial Dysfunction of Newborn"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transient Myocardial Dysfunction of Newborn", "shortest_name_length": 43}
{"curie": "UMLS:C5239576", "names": ["Locally Advanced Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Hepatocellular Carcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0004333", "names": ["Pancreatic ACTH Producing NET", "pancreatic ACTH producing NET", "Pancreatic ACTH Producing Tumor", "pancreatic ACTH producing tumor", "pancreatic ACTH hormone producing tumor", "pancreatic ACTH hormone producing tumour", "Pancreatic ACTH Producing Neuroendocrine Tumor", "pancreatic ACTH producing neuroendocrine tumor", "pancreatic ACTH-producing neuroendocrine tumor", "Pancreatic ACTH-Producing Neuroendocrine Tumor", "Pancreatic Adrenocorticotropic Hormone Producing Tumor", "pancreatic adrenocorticotropic hormone producing tumor", "Ectopic ACTH-Producing Pancreatic Neuroendocrine Tumor", "pancreatic Adrenocorticotropic Hormone Producing tumor", "pancreatic Adrenocorticotropic Hormone Producing tumour", "Pancreatic ACTH-Producing Neuroendocrine Tumor With Cushing Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic ACTH-producing neuroendocrine tumor", "shortest_name_length": 29}
{"curie": "MONDO:0020768", "names": ["DFNX", "X-linked deafness", "deafness, X-linked", "deafness, X-linked, DFN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked deafness", "shortest_name_length": 4}
{"curie": "UMLS:C1335428", "names": ["Plasmacytic Hyperplasia PTLD", "Plasmacytic Hyperplasia Post-Transplant Lymphoproliferative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Plasmacytic Hyperplasia Post-Transplant Lymphoproliferative Disorder", "shortest_name_length": 28}
{"curie": "MONDO:0001152", "names": ["Amnesia", "amnesia", "AMNESIA", "Amnesias", "amnesias", "Forgetful", "forgetful", "Dysmnesia", "dysmnesia", "bad memory", "Bad memory", "memory poor", "memory loss", "MEMORY LOSS", "Amnesia NOS", "Poor memory", "Memory loss", "poor memory", "Memory gone", "Memory Loss", "loss; memory", "Amnesia, NOS", "memory; loss", "Memory Losses", "forgetfulness", "FORGETFULNESS", "Forgetfulness", "impair memory", "loss of memory", "Memory deficit", "LOSS OF MEMORY", "memory problem", "memory deficit", "Memory problem", "lack of memory", "Loss of memory", "MEMORY LOSS OF", "Memory loss of", "Memory Deficit", "Memory problems", "memory disorder", "Impaired Memory", "disorder memory", "impaired memory", "memory deficits", "memory problems", "Memory loss NOS", "Impaired memory", "Memory impaired", "lack of; memory", "Deficit, Memory", "MEMORY IMPAIRED", "memory; lack of", "Memory Disorder", "Memory Deficits", "Memory deficits", "Lack (of);memory", "amnesic syndrome", "memory; disorder", "disorders memory", "Loss (of);memory", "Memory disorders", "Deficits, Memory", "Memory Disorders", "Amnesic syndrome", "memory disorders", "disorder; memory", "Impairment;memory", "amnestic syndrome", "impairment memory", "MEMORY IMPAIRMENT", "AMNESTIC SYNDROME", "Amnestic syndrome", "Amnestic disorder", "Memory Impairment", "Memory impairment", "amnestic disorder", "Amnestic Disorder", "memory impairment", "Amnesia (finding)", "impairments memory", "memory disturbance", "MEMORY DISTURBANCE", "amnestic disorders", "Memory dysfunction", "Amnestic disorders", "Memory disturbance", "Memory Dysfunction", "disturbance; memory", "Amnesia-Memory Loss", "memory; disturbance", "Amnesia Memory Loss", "Forgetful (finding)", "amnesia (diagnosis)", "LOM - loss of memory", "LOM - Loss of memory", "Amnestic disorder NOS", "Amnesia-Memory Losses", "Memory loss - amnesia", "Disturbance of memory", "RNDx memory impairment", "Memory Loss/Impairment", "Amnestic disorder, NOS", "Difficulty;remembering", "syndrome; organic amnesic", "memory loss or impairment", "organic amnestic syndrome", "Memory retention disorder", "Disturbance of memory, NOS", "organic; amnestic syndrome", "Memory impairment (finding)", "Amnestic disorder (disorder)", "Cognitive Retention Disorder", "Retention Disorder, Cognitive", "amnestic disorder (diagnosis)", "Cognitive Retention Disorders", "Retention Disorders, Cognitive", "Disturbance memory/concentration", "Korsakoff's psychosis or syndrome", "RNDx memory impairment (diagnosis)", "Nonalcoholic Korsakoff's psychosis or syndrome", "Amnestic disorder in conditions classified elsewhere"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amnestic disorder", "shortest_name_length": 7}
{"curie": "UMLS:C4521710", "names": ["IIIA", "Stage IIIA Esophageal Adenocarcinoma", "Pathologic Stage IIIA Esophageal Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IIIA Esophageal Adenocarcinoma AJCC v8", "shortest_name_length": 4}
{"curie": "UMLS:C4744570", "names": ["Refractory Blastic Plasmacytoid Dendritic Cell Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Blastic Plasmacytoid Dendritic Cell Neoplasm", "shortest_name_length": 55}
{"curie": "UMLS:C3897755", "names": ["Recurrent Fibrillary Astrocytoma", "recurrent childhood fibrillary astrocytoma", "Recurrent Childhood Fibrillary Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Fibrillary Astrocytoma", "shortest_name_length": 32}
{"curie": "MONDO:0024333", "names": ["ischia", "ischias", "Sciatia", "Sciatica", "SCIATICA", "sciatica", "ischialgia", "Ischialgia", "sciatic neuralgia", "Sciatic Neuralgia", "Sciatic neuralgia", "Cotugno's disease", "Sciatic Neuralgias", "Sciatica neuralgia", "Neuralgia, Sciatic", "neuralgia, sciatic", "sciatic Neuralgias", "bilateral sciatica", "neuralgias, sciatic", "bilateral sciaticas", "sciatica, bilateral", "Sciatica (disorder)", "Neuralgias, Sciatic", "sciatica (diagnosis)", "Sciatica, unspecified side", "Neuralgia-neuritis of sciatic nerve", "Neuralgia or neuritis of sciatic nerve"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sciatica", "shortest_name_length": 6}
{"curie": "MONDO:0004240", "names": ["posterior urethra cancer", "proximal urethral cancer", "posterior urethral cancer", "Posterior Urethra Malignant Tumor", "posterior urethra malignant tumor", "posterior urethral malignant tumor", "Posterior urethral malignant tumor", "Posterior Urethral Malignant Tumor", "malignant tumor of posterior urethra", "Posterior Urethra Malignant Neoplasm", "posterior urethra malignant neoplasm", "Malignant Tumor of Posterior Urethra", "posterior urethral malignant neoplasm", "Posterior Urethral Malignant Neoplasm", "Malignant Neoplasm of Posterior Urethra", "malignant neoplasm of posterior urethra", "Malignant Tumor of the Posterior Urethra", "malignant tumor of the posterior urethra", "Malignant Neoplasm of the Posterior Urethra", "malignant neoplasm of the posterior urethra"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "posterior urethra cancer", "shortest_name_length": 24}
{"curie": "UMLS:C0270091", "names": ["Vacuum extraction chignon", "Vacuum Extraction Chignon", "Chignon from vacuum extraction", "Vacuum extraction chignon (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vacuum extraction chignon", "shortest_name_length": 25}
{"curie": "MONDO:0003022", "names": ["Angiosarcoma", "angiosarcoma", "Childhood Angiosarcoma", "childhood angiosarcoma", "Pediatric Angiosarcoma", "pediatric angiosarcoma", "angiosarcoma, childhood", "angiosarcoma, pediatric", "paediatric angiosarcoma", "pediatric hemangiosarcoma", "childhood hemangiosarcoma", "Childhood Hemangiosarcoma", "Pediatric Hemangiosarcoma", "hemangiosarcoma, pediatric", "sarcoma, angio-, childhood", "hemangiosarcoma, childhood", "sarcoma, angio-, pediatric", "paediatric hemangiosarcoma", "pediatric angiosarcoma (disease)", "childhood angiosarcoma (disease)", "angiosarcoma (disease) of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pediatric angiosarcoma", "shortest_name_length": 12}
{"curie": "MONDO:0030515", "names": ["SPGF63", "SPERMATOGENIC FAILURE 63", "spermatogenic failure 63"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 63", "shortest_name_length": 6}
{"curie": "MONDO:0032672", "names": ["IDDCDF", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES", "intellectual developmental disorder with cardiac defects and dysmorphic facies", "TMEM94-associated congenital heart defect-facial dysmorphism-developmental delay syndrome", "TMEM94-associated congenital heart defect, facial dysmorphism, developmental delay syndrome", "Transmembrane protein 94-associated congenital heart defect, facial dysmorphism, developmental delay syndrome", "Transmembrane protein 94-associated congenital heart defect, facial dysmorphism, developmental delay syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder with cardiac defects and dysmorphic facies", "shortest_name_length": 6}
{"curie": "UMLS:C0919560", "names": ["stent occlusion", "Stent occlusion", "occlusion stent", "Arterial stent occlusion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arterial stent occlusion", "shortest_name_length": 15}
{"curie": "MONDO:0024532", "names": ["OFC", "OFC1", "OTFCS", "otofaciocervical syndrome", "otofaciocervical syndrome 1", "OTOFACIOCERVICAL SYNDROME 1", "EYA1 otofaciocervical syndrome", "otofaciocervical syndrome caused by mutation in EYA1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "otofaciocervical syndrome 1", "shortest_name_length": 3}
{"curie": "UMLS:C2188153", "names": ["USTS", "Undifferentiated sarcoma", "Undifferentiated Sarcoma", "Unclassified Soft Tissue Sarcoma", "Undifferentiated Soft Tissue Sarcoma", "Undifferentiated/Unclassified Sarcoma", "undifferentiated sarcoma of soft tissue", "Undifferentiated/Unclassified Soft Tissue Sarcoma", "undifferentiated sarcoma of soft tissue (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "undifferentiated sarcoma of soft tissue", "shortest_name_length": 4}
{"curie": "UMLS:C1336387", "names": ["Stage IVB Oropharynx Epidermoid Carcinoma", "Stage IVB Oropharyngeal Epidermoid Carcinoma", "Stage IVB Oropharynx Squamous Cell Carcinoma", "Stage IVB Epidermoid Carcinoma of Oropharynx", "Stage IVB Oropharyngeal Squamous Cell Carcinoma", "Stage IVB Squamous Cell Carcinoma of Oropharynx", "Stage IVB Epidermoid Carcinoma of the Oropharynx", "Stage IVB Squamous Cell Carcinoma of the Oropharynx", "Stage IVB Oropharyngeal Throat Squamous Cell Cancer", "Stage IVB Oropharyngeal Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Oropharyngeal Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 41}
{"curie": "MONDO:0035075", "names": ["secondary early-onset glaucoma of genetic origin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary early-onset glaucoma of genetic origin", "shortest_name_length": 48}
{"curie": "MONDO:0007606", "names": ["fop", "FOP", "Münchmeyer", "Münchmeyer disease", "Stone Man Syndrome", "Stone Man syndrome", "Munchmeyer disease", "Stone man syndrome", "MUENCHMEYER SYNDROME", "muenchmeyer syndrome", "Muenchmeyer's syndrome", "progressive ossifying myositis", "Progressive Ossifying Myositis", "Myositis Ossificans Progressiva", "progressive myositis ossificans", "myositis ossificans progressiva", "Progressive myositis ossificans", "Progressive Myositis Ossificans", "MYOSITIS OSSIFICANS PROGRESSIVA", "Myositis ossificans progressiva", "ossificans; myositis, progressiva", "myositis; ossificans, progressiva", "Fibrodysplasia ossificans congenita", "FIBRODYSPLASIA OSSIFICANS PROGRESSIVA", "Fibrodysplasia ossificans progressiva", "fibrodysplasia ossificans progressiva", "Fibrodysplasia Ossificans Progressiva", "ossificans progressiva; fibrodysplasia", "fibrodysplasia; ossificans progressiva", "Progressive myositis ossificans (disorder)", "Diffuse progressive ossifying polymyositis", "Progressive myositis ossificans (diagnosis)", "FOP - Fibrodysplasia ossificans progressiva", "Myositis ossificans progressiva, site unspecified", "Myositis ossificans progressiva, unspecified site", "calcification; muscle, progressive myositis ossificans", "muscle; calcification, progressive myositis ossificans"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibrodysplasia ossificans progressiva", "shortest_name_length": 3}
{"curie": "MONDO:0030538", "names": ["DYT34", "DYSTONIA 34, MYOCLONIC", "dystonia 34, myoclonic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dystonia 34, myoclonic", "shortest_name_length": 5}
{"curie": "MONDO:0033969", "names": ["inflammatory bowel disease-recurrent sinopulmonary infections syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory bowel disease-recurrent sinopulmonary infections syndrome", "shortest_name_length": 70}
{"curie": "MONDO:0018487", "names": ["autosomal recessive severe congenital neutropenia due to CXCR2 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive severe congenital neutropenia due to CXCR2 deficiency", "shortest_name_length": 73}
{"curie": "MONDO:0019240", "names": ["sterol biosynthesis disorder", "inborn error of sterol biosynthetic process", "inborn sterol biosynthetic process disorder", "rare inborn error of sterol biosynthetic process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sterol biosynthesis disorder", "shortest_name_length": 28}
{"curie": "UMLS:C3273072", "names": ["Liver Infantile Hemangioma", "Infantile hemangioma of liver", "Infantile haemangioma of liver", "Liver Infantile Hemangioendothelioma", "Infantile hemangioma of liver (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infantile hemangioma of liver", "shortest_name_length": 26}
{"curie": "MONDO:0001127", "names": ["tibialis tendinitis", "Tibialis tendonitis", "Tibialis tendinitis", "tendinitis of tibialis", "Tibialis tendinitis, NOS", "Tibialis tendinitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tibialis tendinitis", "shortest_name_length": 19}
{"curie": "UMLS:C4725699", "names": ["FA-DLBCL", "Fibrin-Associated Diffuse Large B-Cell Lymphoma", "Fibrin-Associated EBV-Positive Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fibrin-Associated Diffuse Large B-Cell Lymphoma", "shortest_name_length": 8}
{"curie": "MONDO:0004542", "names": ["GCC of the cervix", "glassy cell carcinoma of cervix", "Glassy cell carcinoma of the cervix", "glassy cell carcinoma of the cervix", "glassy cell carcinoma of the cervix uteri", "glassy cell carcinoma of cervix (diagnosis)", "Glassy cell adenocarcinoma of the uterine cervix", "glassy cell adenocarcinoma of the uterine cervix", "glassy cell variant cervical adenosquamous carcinoma", "cervical adenosquamous carcinoma, glassy cell variant", "Cervical Adenosquamous Carcinoma, Glassy Cell Variant", "Cervical Poorly Differentiated Adenosquamous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical adenosquamous carcinoma, glassy cell variant", "shortest_name_length": 17}
{"curie": "MONDO:0014663", "names": ["SRS3", "GRDF", "Silver-Russell syndrome 3", "SILVER-RUSSELL SYNDROME 3", "growth restriction, severe, with distinctive facies", "GROWTH RESTRICTION, SEVERE, WITH DISTINCTIVE FACIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Silver-Russell syndrome 3", "shortest_name_length": 4}
{"curie": "MONDO:0024539", "names": ["CACD1", "choroidal sclerosis", "choroidal dystrophy, central areolar", "CENTRAL AREOLAR CHOROIDAL DYSTROPHY 1", "Choroidal Dystrophy, Central Areolar 1", "choroidal dystrophy, central areolar 1", "choroidal dystrophy, central areolar, 1", "CHOROIDAL DYSTROPHY, CENTRAL AREOLAR, 1", "GUCY2D central areolar choroidal dystrophy", "central areolar choroidal dystrophy caused by mutation in GUCY2D"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choroidal dystrophy, central areolar, 1", "shortest_name_length": 5}
{"curie": "MONDO:0008740", "names": ["AGOTC", "otocephaly", "Otocephaly", "OTOCEPHALY", "Otocephalus", "Dysgnathia complex", "Otocephalic syndrome", "Agnathia-holoprosencephaly", "Holoprosencephaly-agnathia", "HOLOPROSENCEPHALY-AGNATHIA", "holoprosencephaly-agnathia", "agnathia-holoprosencephaly", "Agnathia-otocephaly complex", "AGNATHIA-OTOCEPHALY COMPLEX", "agnathia-otocephaly complex", "Otocephalic syndrome (disorder)", "Dysgnathia Complex agnathia-holoprosencephaly", "dysgnathia complex agnathia-holoprosencephaly", "DYSGNATHIA COMPLEX AGNATHIA-HOLOPROSENCEPHALY", "agnathia-holoprosencephaly-situs inversus syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "agnathia-otocephaly complex", "shortest_name_length": 5}
{"curie": "UMLS:C0854351", "names": ["Renal failure neonatal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal failure neonatal", "shortest_name_length": 22}
{"curie": "MONDO:0006734", "names": ["neoplasm of duodenum", "Benign Duodenal Tumor", "benign duodenal tumor", "Benign duodenal tumor", "duodenum benign neoplasm", "Benign duodenal neoplasm", "Benign Duodenal Neoplasm", "Benign tumor of duodenum", "benign tumor of duodenum", "Benign Tumor of Duodenum", "neoplasm of the duodenum", "benign duodenal neoplasm", "duodenal benign neoplasm", "Benign tumour of duodenum", "benign neoplasm of duodenum", "Benign neoplasm of duodenum", "Benign Neoplasm of Duodenum", "benign tumor of the duodenum", "Benign Tumor of the Duodenum", "benign neoplasm of the duodenum", "Benign Neoplasm of the Duodenum", "Benign neoplasm of duodenum (disorder)", "benign neoplasm of duodenum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign duodenal neoplasm", "shortest_name_length": 20}
{"curie": "UMLS:C1699177", "names": ["gastrointestinal stoma stenosis", "Gastrointestinal Stoma Stenosis", "Stenosis of gastrointestinal stoma", "gastrointestinal stoma stenosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal Stoma Stenosis", "shortest_name_length": 31}
{"curie": "UMLS:C0521478", "names": ["mucocutaneous ulcer", "MUCOCUTANEOUS ULCER", "Mucocutaneous ulcer", "mucocutaneous ulcers", "Mucocutaneous ulceration", "mucocutaneous ulceration", "Mucocutaneous ulcer, NOS", "MUCOCUTANEOUS ULCERATION", "Mucocutaneous ulcer (disorder)", "Mucocutaneous ulcer (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mucocutaneous ulcer", "shortest_name_length": 19}
{"curie": "MONDO:0003656", "names": ["HEMOGLOBINURIA", "Hemoglobinuria", "hemoglobinuria", "haemoglobinuria", "hemoglobin uria", "Haemoglobinuria", "Hemoglobin in urine", "Hemoglobinuria, NOS", "Haemoglobinuria, NOS", "Haemoglobin in urine", "Hemoglobinuria (finding)", "hemoglobin positive urine", "hemoglobinuria (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemoglobinuria", "shortest_name_length": 14}
{"curie": "MONDO:0021394", "names": ["polyp vagina", "vagina polyp", "Vaginal Polyp", "Vaginal polyp", "polyp; vagina", "vagina; polyp", "vaginal polyp", "polyp vaginal", "polyps vagina", "VAGINAL POLYP", "polyps vaginal", "Polyp of vagina", "polyp of vagina", "Polyp of Vagina", "Polyp of the Vagina", "polyp of the vagina", "polyp, vaginal, benign", "POLYP, VAGINAL, BENIGN", "Polyp of vagina (disorder)", "polyp of vagina (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyp of vagina", "shortest_name_length": 12}
{"curie": "UMLS:C4330256", "names": ["HNF4A-Associated Hyperinsulinism", "Hepatocyte Nuclear Factor 4-Alpha Hyperinsulinism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatocyte Nuclear Factor 4-Alpha Hyperinsulinism", "shortest_name_length": 32}
{"curie": "UMLS:C4744986", "names": ["Advanced Gastric Small Cell Carcinoma", "Advanced Gastric Small Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Gastric Small Cell Neuroendocrine Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0017586", "names": ["onychocytic matricoma", "acanthoma of the nail matrix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "onychocytic matricoma", "shortest_name_length": 21}
{"curie": "MONDO:0044995", "names": ["Parasympathetic Disorders", "parasympathetic nervous system disease", "parasympathetic nervous system disorder", "Parasympathetic Nervous System Diseases", "Nervous System Diseases, Parasympathetic", "nervous system; disorder, parasympathetic", "disease of parasympathetic nervous system", "Disorder of parasympathetic nervous system", "disorder of parasympathetic nervous system", "Disorder of parasympathetic nervous system, NOS", "parasympathetic nervous system disease or disorder", "Disorder of parasympathetic nervous system (disorder)", "disease or disorder of parasympathetic nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parasympathetic nervous system disorder", "shortest_name_length": 25}
{"curie": "MONDO:0000408", "names": ["FASD", "FASDs", "fetal alcohol syndrome", "syndrome, fetal alcohol", "FAE (fetal alcohol effects)", "FAEs (fetal alcohol effects)", "alcohol related birth defects", "alcohol-related birth defects", "birth defects, alcohol-related", "partial fetal alcohol syndrome", "fetal alcohol spectrum disorder", "Fetal alcohol spectrum disorder", "Fetal Alcohol Spectrum Disorder", "fetal alcohol spectrum disorders", "Fetal Alcohol Spectrum Disorders", "Foetal alcohol spectrum disorder", "Foetal Alcohol Spectrum Disorder", "fetal alcohol syndrome (FAS) - type", "Fetal Alcohol Spectrum Disorder (disorder)", "alcohol related neurodevelopmental disorder", "alcohol-related birth defects (ARBD) - type", "alcohol-related neurodevelopmental disorder (ARND) - type", "growth retardation, facial abnormalities, and central nervous system dysfunction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fetal alcohol spectrum disorder", "shortest_name_length": 4}
{"curie": "MONDO:0005959", "names": ["Sick House Syndrome", "Syndrome, Sick House", "Syndromes, Sick House", "Sick Building Syndrome", "Sick building syndrome", "sick building syndrome", "Syndrome, Sick Building", "building sick syndromes", "Sick building syndrome (disorder)", "sick building syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sick building syndrome", "shortest_name_length": 19}
{"curie": "UMLS:C0220613", "names": ["adult STS", "STS, adult", "Soft Tissue Sarcoma", "soft tissue sarcoma adult", "Adult Soft Tissue Sarcoma", "adult soft tissue sarcoma", "Soft tissue sarcoma, adult", "soft tissue sarcoma, adult", "sarcoma, adult soft tissue", "Adult Sarcoma of Soft Tissue", "Adult Sarcoma of the Soft Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Soft Tissue Sarcoma", "shortest_name_length": 9}
{"curie": "MONDO:0016064", "names": ["Uranoschisis", "cleft palate", "PALATE CLEFT", "CLEFT PALATE", "Cleft palate", "Cleft-palate", "Cleft Palate", "Palate cleft", "cleft palates", "Cleft Palates", "palatoschisis", "palate; cleft", "Palatoschisis", "cleft; palate", "Palate, Cleft", "Palates, Cleft", "Cleft of palate", "Cleft palate NOS", "Cleft palate, NOS", "CP - Cleft palate", "Cleft roof of mouth", "Uranostaphyloschisis", "uranostaphyloschisis", "Cleft secondary palate", "secondary cleft palate", "Cleft palate (disorder)", "cleft palate (diagnosis)", "Cleft of secondary palate", "Cleft palate, unspecified", "Cleft hard and soft palate", "cleft; palate, hard and soft", "cleft; palate, soft with hard", "Cleft of hard and soft palate", "cleft hard palate and soft palate", "deformity; palate, cleft (congenital)", "Cleft hard and soft palate (disorder)", "cleft hard palate with cleft soft palate", "Cleft hard palate with cleft soft palate", "cleft hard palate with cleft soft palate (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleft palate", "shortest_name_length": 12}
{"curie": "UMLS:C0917817", "names": ["Neurofibromatosis 3", "Neurofibromatosis 3s", "Neurofibromatosis Type 3", "Neurofibromatosis type 3", "Type 3, Neurofibromatosis", "Neurofibromatosis Type 3s"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neurofibromatosis 3", "shortest_name_length": 19}
{"curie": "UMLS:C1336828", "names": ["True Thymic Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "True Thymic Hyperplasia", "shortest_name_length": 23}
{"curie": "UMLS:C5204532", "names": ["Recurrent Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Adenocarcinoma", "shortest_name_length": 24}
{"curie": "MONDO:0001005", "names": ["Kaolinosis", "kaolinosis", "simple kaolinosis", "Kaolin pneumoconiosis", "Kaolinosis (disorder)", "Kaolin Pneumoconiosis", "kaolin pneumoconiosis", "kaolin; pneumoconiosis", "kaolinosis (diagnosis)", "pneumoconiosis; kaolin", "pneumoconiosis due to kaolin", "Kaolin workers pneumoconiosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kaolin pneumoconiosis", "shortest_name_length": 10}
{"curie": "UMLS:C0702109", "names": ["Erythropoiesis abnormal", "Abnormal erythrocyte maturation", "Abnormal erythrocyte production", "Erythrocyte production, abnormal", "Abnormal erythrocyte production (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abnormal erythrocyte production", "shortest_name_length": 23}
{"curie": "MONDO:0004985", "names": ["BPAD", "MAFD", "manic disorder", "bipolar illness", "manic depressive", "bipolar disorder", "Bipolar disorder", "Manic depression", "Manic-Depression", "Disorder;bipolar", "Manic depressive", "manic depression", "manic-depression", "Manic Depression", "Depression;manic", "Bipolar Disorder", "BIPOLAR DISORDER", "manic depressions", "BIPOLAR DISORDERS", "Bipolar Disorders", "bipolar; disorder", "Bi-polar Disorder", "disorder; bipolar", "Disorder, Bipolar", "Bipolar disorders", "bipolar disorders", "bipolar depression", "bipolar disorder nos", "bipolar disorder NOS", "Bipolar disorder NOS", "Bipolar disorder, NOS", "bipolar mood disorder", "Bipolar Mood Disorder", "Disorder, Bipolar Mood", "Bipolar Mood Disorders", "mixed bipolar disorder", "Mood Disorder, Bipolar", "depressive-manic psych.", "Depressive-manic psych.", "Mixed bipolar I disorder", "Manic-depressive illness", "manic-depressive illness", "Manic-Depressive Illness", "MANIC DEPRESSIVE ILLNESS", "Manic bipolar I disorder", "manic bipolar I disorder", "major affective disorder", "manic depressive illness", "Manic depressive illness", "obsolete_bipolar disorder", "manic depressive disorder", "Manic Depressive disorder", "Manic Depressive Disorder", "REACTION MANIC-DEPRESSIVE", "MANIC DEPRESSIVE REACTION", "manic-depressive reaction", "Reaction manic-depressive", "Manic depressive reaction", "Manic depressive psychosis", "Bipolar Affective Disorder", "manic-depressive psychosis", "manic-depressive; disorder", "syndrome; manic-depressive", "Manic Depressive Psychosis", "Psychosis manic-depressive", "manic-depressive; syndrome", "PSYCHOSIS MANIC-DEPRESSIVE", "manic depressive psychosis", "manic-depressive disorders", "Psychosis;manic depressive", "Bipolar affective disorder", "Manic-Depressive Psychosis", "Manic-depressive psychosis", "BIPOLAR AFFECTIVE DISORDER", "bipolar affective disorder", "affective bipolar disorder", "psychosis; manic-depressive", "bipolar affective psychosis", "Bipolar Affective Psychosis", "Psychosis, Manic Depressive", "Psychoses, Manic-Depressive", "Psychosis, Manic-Depressive", "Bipolar disorder (disorder)", "manic-depressive; psychosis", "Psychoses, Manic Depressive", "affective bipolar disorders", "Affective Psychosis, Bipolar", "bipolar; disorder, affective", "Psychoses, Bipolar Affective", "Psychosis, Bipolar Affective", "disorder; bipolar, affective", "bipolar disorder manic phase", "Manic-depressive syndrome NOS", "Manic-depressive reaction NOS", "Bipolar disorder, unspecified", "Mixed bipolar I disorder, NOS", "MDI - Manic-depressive illness", "manic bipolar affective disorder", "bipolar disorder NOS (diagnosis)", "major bipolar affective disorder", "Manic Bipolar Affective disorder", "Mixed bipolar I disorder (disorder)", "Bipolar affective disorder, unspecified", "Bipolar I disorder, most recent episode mixed", "bipolar I disorder, most recent episode, mixed", "disorder; bipolar, I, most recent episode, mixed", "Bipolar affective disorder, mixed, unspecified degree", "bipolar I disorder, most recent episode, mixed (diagnosis)", "Bipolar I disorder, most recent episode (or current) mixed, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bipolar disorder", "shortest_name_length": 4}
{"curie": "MONDO:0006029", "names": ["Cecum Cancer", "cecal cancer", "Cecal cancer", "Cecal Cancer", "cecum cancer", "cecal carcinoma", "Cecum Carcinoma", "cecum carcinoma", "Cecal Carcinoma", "CECAL CARCINOMA", "carcinoma cecum", "caecum carcinoma", "Caecum carcinoma", "carcinoma of cecum", "Carcinoma of Cecum", "Carcinoma of cecum", "Carcinoma of caecum", "carcinoma of caecum", "carcinoma of the cecum", "Carcinoma of the Cecum", "Carcinoma of cecum (disorder)", "Carcinoma of cecum (diagnosis)", "malignant large intestine neoplasm of cecum carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cecum carcinoma", "shortest_name_length": 12}
{"curie": "UMLS:C2983713", "names": ["Cutaneous Melanoma by AJCC v6 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous Melanoma by AJCC v6 Stage", "shortest_name_length": 35}
{"curie": "MONDO:0010430", "names": ["MRXZ", "Mrxz", "MRX65", "MRX97", "XLID97", "X-linked mental retardation 97", "X-linked mental retardation 65", "MENTAL RETARDATION, X-LINKED 97", "mental retardation, X-linked 97", "Mental retardation, X-linked 97", "mental retardation, X-linked 65", "MENTAL RETARDATION, X-LINKED 65", "intellectual disability, X-linked 97", "intellectual disability, X-linked 65", "mental retardation, X-linked type 97", "intellectual disability, X-linked type 97", "Mental Retardation, X-Linked, Znf711-Related", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 97", "intellectual developmental disorder, X-linked 97", "non-syndromic X-linked intellectual disability 97", "ZNF711 non-syndromic X-linked intellectual disability", "non-syndromic X-linked intellectual disability caused by mutation in ZNF711"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 97", "shortest_name_length": 4}
{"curie": "MONDO:0020507", "names": ["Cree leukoencephalopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cree leukoencephalopathy", "shortest_name_length": 24}
{"curie": "UMLS:C2024309", "names": ["Heart Diffuse Large B-Cell Lymphoma", "Cardiac Diffuse Large B-Cell Lymphoma", "large B-cell diffuse lymphoma of heart", "Primary Heart Diffuse Large B-Cell Lymphoma", "Primary Cardiac Diffuse Large B-Cell Lymphoma", "large B-cell diffuse lymphoma of heart (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "large B-cell diffuse lymphoma of heart", "shortest_name_length": 35}
{"curie": "MONDO:0015378", "names": ["Fourth branchial cleft cyst", "fourth branchial cleft cyst", "Type 4 branchial cleft cyst", "fourth branchial cleft fistula", "fourth branchial cleft anomaly", "Fourth branchial cleft fistula", "Fourth branchial cleft anomaly", "Fourth branchial cleft cyst (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fourth branchial cleft anomaly", "shortest_name_length": 27}
{"curie": "MONDO:0002994", "names": ["Pancreatic Delta Cell NET", "pancreatic Delta cell NET", "Pancreatic Delta Cell Tumor", "pancreatic Delta cell tumor", "pancreatic delta cell neoplasm", "pancreatic Delta cell neoplasm", "Pancreatic Delta Cell Neoplasm", "Pancreatic Delta Cell Neuroendocrine Tumor", "pancreatic delta cell neuroendocrine tumor", "pancreatic Delta cell neuroendocrine tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic delta cell neuroendocrine tumor", "shortest_name_length": 25}
{"curie": "UMLS:C0280822", "names": ["Localized Unresectable Neuroblastoma", "localized unresectable neuroblastoma", "neuroblastoma, localized unresectable"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized Unresectable Neuroblastoma", "shortest_name_length": 36}
{"curie": "MONDO:0008840", "names": ["AT", "ATA", "AT1", "ATD", "ATC", "ATE", "Louis-Bar", "Louis-Bar disease", "louis-bar syndrome", "Louis Bar syndrome", "LOUIS-BAR SYNDROME", "Louis-Bar Syndrome", "Louis Bar Syndrome", "Louis-Bar syndrome", "louis bar syndrome", "Syndrome, Louis-Bar", "Ataxia telangiectasia", "Ataxia-telangiectasia", "ataxia telangiectasia", "ATAXIA-TELANGIECTASIA", "Ataxia-Telangiectasia", "Ataxia Telangiectasia", "ataxia-telangiectasia", "ATAXIA, TELANGIECTASIA", "telangiectasia; ataxia", "ataxia; telangiectasia", "Boder-Sedgwick syndrome", "ataxia - telangiectasia", "boder-Sedgwick syndrome", "AT, complementation group C", "AT, complementation group D", "AT, complementation group E", "AT, COMPLEMENTATION GROUP A", "AT, COMPLEMENTATION GROUP C", "AT, COMPLEMENTATION GROUP D", "AT, COMPLEMENTATION GROUP E", "AT, complementation group A", "ataxia telangiectasia syndrome", "Ataxia-telangiectasia syndrome", "Ataxia telangiectasia syndrome", "Ataxia Telangiectasia Syndrome", "Syndrome, Ataxia Telangiectasia", "ataxia - telangiectasia variant", "ataxia telangiectasia (diagnosis)", "cerebello-oculocutaneous telangiectasia", "Telangiectasia, Cerebello-Oculocutaneous", "TELANGIECTASIA, CEREBELLO-OCULOCUTANEOUS", "ataxia telangiectasia (Louis-Bar disease)", "Ataxia-telangiectasia syndrome (disorder)", "immunodeficiency with ataxia telangiectasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ataxia telangiectasia", "shortest_name_length": 2}
{"curie": "MONDO:0010295", "names": ["OLEDAID", "OL-EDA-ID", "ol-EDA-ID", "OL-EDA-ID Syndrome", "anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome", "Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome", "Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome", "Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema", "Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphoedema syndrome", "ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema", "ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH IMMUNODEFICIENCY, OSTEOPETROSIS, AND LYMPHEDEMA", "Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome (disorder)", "OL-EDA-ID (anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema) syndrome", "Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome (diagnosis)", "OL-EDA-ID (anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphoedema) syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome", "shortest_name_length": 7}
{"curie": "UMLS:C1562687", "names": ["Medulloepithelioma, benign", "Benign Intraocular Medulloepithelioma", "Benign intraocular medulloepithelioma", "Ciliary Body Benign Medulloepithelioma", "Benign Ciliary Body Medulloepithelioma", "Benign medulloepithelioma of ciliary body", "Benign intraocular medulloepithelioma (disorder)", "Benign medulloepithelioma of ciliary body (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign medulloepithelioma of ciliary body", "shortest_name_length": 26}
{"curie": "MONDO:0005278", "names": ["serous carcinoma", "Serous carcinoma", "Serous Adenocarcinoma", "serous adenocarcinoma", "Serous adenocarcinoma", "Serous cystadenocarcinoma", "Serous Cystadenocarcinoma", "serous cystadenocarcinoma", "Cystadenocarcinoma, Serous", "Serous Cystadenocarcinomas", "Serous adenocarcinoma, NOS", "Cystadenocarcinomas, Serous", "Serous cystadenocarcinoma NOS", "Serous cystadenocarcinoma, NOS", "Papillary serous adenocarcinoma", "Serous surface papillary carcinoma", "Papillary serous cystadenocarcinoma", "Serous carcinoma (morphologic abnormality)", "serous cystadenocarcinoma, NOS (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "serous adenocarcinoma", "shortest_name_length": 16}
{"curie": "MONDO:0009918", "names": ["PFD Lavia type", "PFD, LAVIA TYPE", "Pfd, Lavia type", "PFD, FINNISH TYPE", "Pfd, Finnish type", "pseudoinflammatory fundus dystrophy", "Pseudoinflammatory fundus dystrophy, Finnish type", "Fundus dystrophy, pseudoinflammatory recessive form", "fundus dystrophy, pseudoinflammatory recessive form", "Fundus Dystrophy, Pseudoinflammatory, Recessive Form", "FUNDUS DYSTROPHY, PSEUDOINFLAMMATORY, RECESSIVE FORM", "fundus dystrophy, pseudoinflammatory, recessive form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fundus dystrophy, pseudoinflammatory, recessive form", "shortest_name_length": 14}
{"curie": "UMLS:C5554730", "names": ["Poorly Differentiated Chordoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Poorly Differentiated Chordoma", "shortest_name_length": 30}
{"curie": "MONDO:0024477", "names": ["hepatoma", "Hepatoma", "Liver tumor", "liver tumor", "Tumor liver", "TUMOR LIVER", "tumor liver", "LIVER TUMOR", "liver tumors", "tumour liver", "Tumour liver", "liver tumour", "Liver tumour", "Liver cancer", "Liver--Tumors", "hepatic tumor", "Hepatic tumor", "liver tumours", "Liver Neoplasm", "Tumor of liver", "Hepatic tumour", "hepatic tumors", "Neoplasm liver", "tumor of liver", "liver neoplasm", "hepatic tumour", "NEOPLASM LIVER", "Liver neoplasm", "Liver neoplasms", "Liver Neoplasms", "hepatics tumors", "hepatic tumours", "liver neoplasms", "Liver tumor NOS", "Neoplasm, Liver", "Tumour of liver", "Neoplasms, Liver", "Hepatic neoplasm", "Hepatic Neoplasm", "Liver tumour NOS", "HEPATIC NEOPLASM", "hepatic neoplasm", "neoplasm of liver", "HEPATIC NEOPLASIA", "Hepatic Neoplasms", "Neoplasm of liver", "hepatic neoplasms", "Hepatic neoplasia", "Neoplasm, Hepatic", "Neoplasm of Liver", "Neoplasms, Hepatic", "hepatic neoplasias", "Hepatic neoplasm NOS", "liver benign neoplasm", "Neoplasm of the liver", "Liver tumor no subtype", "liver neoplasm (disease)", "Neoplasm of liver (disorder)", "neoplasm of liver (diagnosis)", "liver and intrahepatic bile duct neoplasm", "Liver and Intrahepatic Bile Duct Neoplasm", "hepatic and intrahepatic bile duct neoplasm", "Hepatic and Intrahepatic Bile Duct Neoplasm", "Liver tumor no subtype (morphologic abnormality)", "Liver and Intrahepatic Bile Duct Epithelial Neoplasm", "liver and intrahepatic bile duct epithelial neoplasm", "epithelial hepatic and intrahepatic bile duct neoplasm", "Epithelial Hepatic and Intrahepatic Bile Duct Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "liver and intrahepatic bile duct neoplasm", "shortest_name_length": 8}
{"curie": "UMLS:C5419665", "names": ["Advanced Uterine Corpus Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Uterine Corpus Cancer", "shortest_name_length": 30}
{"curie": "UMLS:C4553750", "names": ["Stage IV Penile Cancer", "Stage IV Penile Cancer AJCC v8", "Stage IV Penile Squamous Cell Carcinoma AJCC v8", "Stage IV Squamous Cell Carcinoma of the Penis AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Penile Cancer AJCC v8", "shortest_name_length": 22}
{"curie": "MONDO:0012474", "names": ["BFIS6", "ENFL4", "BFIC6", "nocturnal frontal lobe epilepsy-4", "nocturnal frontal lobe epilepsy 4", "EPILEPSY, NOCTURNAL FRONTAL LOBE, 4", "epilepsy, nocturnal frontal lobe, 4", "benign familial infantile seizures 6", "Benign Familial Infantile Seizures, 6", "SEIZURES, BENIGN FAMILIAL INFANTILE, 6", "seizures, benign familial infantile, 6", "epilepsy, nocturnal frontal lobe, type 4", "Epilepsy, Nocturnal Frontal Lobe, Type 4", "CONVULSIONS, BENIGN FAMILIAL INFANTILE, 6", "convulsions, benign familial infantile, 6", "Autosomal dominant nocturnal frontal lobe epilepsy", "autosomal dominant nocturnal frontal lobe epilepsy 4", "CHRNA2 autosomal dominant nocturnal frontal lobe epilepsy", "autosomal dominant nocturnal frontal lobe epilepsy type 4", "EPILEPSY, FAMILIAL, WITH NOCTURNAL WANDERING AND ICTAL FEAR", "Epilepsy, Familial, with Nocturnal Wandering and Ictal Fear", "epilepsy, familial, with nocturnal wandering and Ictal fear", "autosomal dominant nocturnal frontal lobe epilepsy caused by mutation in CHRNA2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nocturnal frontal lobe epilepsy 4", "shortest_name_length": 5}
{"curie": "UMLS:C1504343", "names": ["Acarodermatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acarodermatitis", "shortest_name_length": 15}
{"curie": "UMLS:C1706734", "names": ["Advanced Unfavorable Non-Hodgkin Lymphoma", "Advanced Unfavorable Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Unfavorable Non-Hodgkin Lymphoma", "shortest_name_length": 41}
{"curie": "MONDO:0010278", "names": ["MRXSCH", "MRXS Christianson", "Christianson Syndrome", "Christianson syndrome", "Angelman-like syndrome X-linked", "X-linked Angelman-like syndrome", "ANGELMAN-LIKE SYNDROME, X-LINKED", "Angelman-like syndrome, X-linked", "Angelman-Like Syndrome, X-Linked", "Christianson syndrome (diagnosis)", "Mental retardation X-linked, South African type", "Intellectual Deficit, X-Linked, South African Type", "X-linked intellectual disability, South African type", "Mental Retardation, X-Linked Syndromic, Christianson Type", "mental retardation, X-linked syndromic, Christianson type", "mental retardation, X-linked, syndromic, Christianson type", "MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE", "Mental Retardation, X-Linked, Syndromic, Christianson Type", "intellectual disability X-linked syndromic Christianson type", "intellectual disability, X-linked syndromic, Christianson type", "X-linked intellectual developmental disorder Christianson type", "intellectual disability, X-linked, syndromic, Christianson type", "MENTAL RETARDATION, MICROCEPHALY, EPILEPSY, AND ATAXIA SYNDROME", "mental retardation, microcephaly, epilepsy, and ataxia syndrome", "Mental Retardation, Microcephaly, Epilepsy, and Ataxia Syndrome", "intellectual disability microcephaly epilepsy and ataxia syndrome", "intellectual disability, microcephaly, epilepsy, and ataxia syndrome", "X-linked intellectual developmental disorder Christianson type (disorder)", "intellectual developmental disorder, X-linked syndromic, Christianson type", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE", "X-linked intellectual disability - craniofacial dysmorphism - epilepsy - ophthalmoplegia - cerebellar atrophy", "X-linked intellectual disability-craniofacial dysmorphism-epilepsy-ophthalmoplegia-cerebellar atrophy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Christianson syndrome", "shortest_name_length": 6}
{"curie": "EFO:0008505", "names": ["hepatitis virus-related hepatocellular carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatitis virus-related hepatocellular carcinoma", "shortest_name_length": 48}
{"curie": "MONDO:0100011", "names": ["Tendonosis", "tendinosis", "Tendinosis", "Tendinoses", "Tendonoses", "Tendinosis (disorder)", "tendinosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tendinosis", "shortest_name_length": 10}
{"curie": "UMLS:C2827448", "names": ["Childhood Diabetes Mellitus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Diabetes Mellitus", "shortest_name_length": 27}
{"curie": "MONDO:0010409", "names": ["MRXS9", "Mental Retardation, X-Linked, Syndromic 9", "MENTAL RETARDATION, X-LINKED, SYNDROMIC 9", "mental retardation, X-linked, syndromic 9", "intellectual disability, X-linked, syndromic 9", "X-linked intellectual disability, Shrimpton type", "syndromic X-linked intellectual disability Shrimpton type", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic X-linked intellectual disability Shrimpton type", "shortest_name_length": 5}
{"curie": "EFO:1001976", "names": ["cardioembolic stroke"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardioembolic stroke", "shortest_name_length": 20}
{"curie": "MONDO:0005277", "names": ["Migraine", "MIGRAINE", "migraine", "MIGRAINES", "Migraines", "migraines", "migraine nos", "Migraine NOS", "Migraine, NOS", "Migraine Variant", "migraine variant", "migraine headache", "MIGRAINE HEADACHE", "migraine syndrome", "migraine disorder", "Variant, Migraine", "HEADACHE MIGRAINE", "MIGRAINE SYNDROME", "Headache;migraine", "Migraine Variants", "Migraine headache", "Migraine Headache", "Migraine Disorder", "disorder migraine", "migraines variant", "migraine variants", "Migraine variants", "migraine; headache", "Variants, Migraine", "migraine headaches", "HEADACHE, MIGRAINE", "Migraine Disorders", "Migraine headaches", "migraine; syndrome", "Disorder, Migraine", "migraine syndromes", "disorders migraine", "Migraine Headaches", "Headache, Migraine", "syndrome; migraine", "headache migraines", "headache; migraine", "Migrainous headache", "Headaches, Migraine", "HEADACHE MIGRAINOUS", "Migraine (disorder)", "Disorders, Migraine", "Migraine, unspecified", "Migraine type headaches", "obsolete_migraine disorder", "Migraine variants (disorder)", "migraine headache (diagnosis)", "migraine with or without aura", "migraine variants (diagnosis)", "HEADACHE MIGRAINE INTERMITTENT", "Intermittent migraine headaches"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "migraine disorder", "shortest_name_length": 8}
{"curie": "UMLS:C0855247", "names": ["sleep attack", "Sleep attack", "attack sleep", "attacks sleep", "Sleep attacks", "sleep attacks", "attacks sleeping", "sleep disorder attack", "Sleep attack (disorder)", "Sleep attack (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sleep attack", "shortest_name_length": 12}
{"curie": "MONDO:0021666", "names": ["otitis", "OTITIS", "Otitis", "Otitides", "Otitis, NOS", "ear infection", "EAR INFECTION", "Ear Infection", "Infection;ear", "Ear infection", "ear infections", "Ear infections", "Ear Infections", "infection; ear", "Infection, Ear", "ear; infection", "Ear--Infections", "Infections, Ear", "Inflammation;ear", "Ear Inflammation", "infection of ear", "Ear inflammation", "Infection of ear", "ear inflammation", "inflammation ear", "EAR INFLAMMATION", "Ear Inflammations", "EAR INFECTION NOS", "inflammation; ear", "Otitis (disorder)", "Ear infection NOS", "ear inflammations", "Inflammation, Ear", "ear; inflammation", "Inflammations, Ear", "Inflammation of ear", "inflammation of the ear", "Infection of ear (disorder)", "infection of ear (diagnosis)", "Inflammatory disorder of ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ear infection", "shortest_name_length": 6}
{"curie": "UMLS:C3899642", "names": ["Childhood Salivary Gland Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Salivary Gland Carcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0005815", "names": ["PNET", "PNEN", "PanNEN", "pancreatic NEN", "Pancreatic NEN", "Pancreatic NET", "Nesidioblastoma", "NESIDIOBLASTOMA", "nesidioblastoma", "Islet Cell Tumor", "Islet cell tumor", "islet cell tumor", "Nesidioblastomas", "islet cell tumour", "Islet Cell Tumors", "Island Cell Tumor", "Islet cell tumour", "islet cell tumors", "Islet cell tumors", "Tumor, Islet Cell", "Islet Cell Adenoma", "Island Cell Tumors", "islet cell adenoma", "Tumors, Islet Cell", "Islet cell adenoma", "Tumor, Island Cell", "Tumors, Island Cell", "Islet cell neoplasm", "islet cell neoplasm", "Islet Cell Adenomas", "Adenoma, Islet Cell", "Adenomas, Islet Cell", "Langerhans Tumor Islet", "Tumor Islet, Langerhans", "Islet cell tumor, benign", "endocrine pancreas tumor", "Islet cell tumour, benign", "pancreas; nesidioblastoma", "Islet of Langerhans tumor", "endocrine pancreas tumors", "Islet of Langerhans Tumor", "cancer endocrine pancreas", "endocrine pancreas cancer", "nesidioblastoma; pancreas", "pancreatic endocrine tumor", "islet cell tumor; pancreas", "pancreas; islet cell tumor", "Pancreatic endocrine tumor", "endocrine pancreatic tumors", "tumor of endocrine pancreas", "Tumor of endocrine pancreas", "pancreas; tumor, islet cell", "Pancreatic endocrine tumour", "tumor; islet cell, pancreas", "islet cell; tumor, pancreas", "endocrine pancreas neoplasm", "pancreatic endocrine cancer", "endocrine pancreatic cancer", "Tumour of endocrine pancreas", "Pancreatic Islet Cell Tumors", "pancreatic Endocrine neoplasm", "pancreatic endocrine neoplasm", "Pancreatic Endocrine Neoplasm", "neoplasm of endocrine pancreas", "Neoplasm of endocrine pancreas", "pancreatic neuroendocrine tumor", "Pancreatic neuroendocrine tumor", "neuroendocrine tumor of pancreas", "neoplasm of islets of Langerhans", "Neoplasm of islets of Langerhans", "Pancreatic neuroendocrine tumour", "Neuroendocrine tumor of pancreas", "Neuroendocrine tumour of pancreas", "nesidioblastoma; unspecified site", "Pancreatic Neuroendocrine Neoplasm", "pancreatic neuroendocrine neoplasm", "Pancreatic neuroendocrine neoplasm", "Pancreatic endocrine tumor, benign", "Well-differentiated pancreatic NEN", "neuroendocrine neoplasm of pancreas", "Neuroendocrine neoplasm of pancreas", "Pancreatic endocrine tumour, benign", "Well-differentiated NEN of pancreas", "malignant pancreatic endocrine tumor", "malignant pancreatic Endocrine tumor", "endocrine pancreas neoplasm (disease)", "malignant pancreatic Endocrine tumour", "malignant tumor of endocrine pancreas", "Malignant tumor of endocrine pancreas", "Malignant tumour of endocrine pancreas", "malignant tumour of endocrine pancreas", "Malignant neoplasm of endocrine pancreas", "malignant neoplasm of endocrine pancreas", "Neoplasm of endocrine pancreas (disorder)", "Islet cell tumor (morphologic abnormality)", "Neuroendocrine tumor of pancreas (disorder)", "neuroendocrine tumor of pancreas (diagnosis)", "neoplasm of islets of Langerhans (diagnosis)", "Islet cell adenoma (morphologic abnormality)", "Islet cell neoplasm (morphologic abnormality)", "pancreatic neoplasm malignant endocrine pancreas", "Malignant tumor of endocrine pancreas (disorder)", "malignant neoplasm of endocrine pancreas (diagnosis)", "Well-differentiated pancreatic neuroendocrine neoplasm", "Well-differentiated neuroendocrine neoplasm of pancreas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic neuroendocrine neoplasm", "shortest_name_length": 4}
{"curie": "UMLS:C5419903", "names": ["Liver and Intrahepatic Bile Duct Soft Tissue Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liver and Intrahepatic Bile Duct Soft Tissue Neoplasm", "shortest_name_length": 53}
{"curie": "UMLS:C0434010", "names": ["Bronchial Injury", "bronchus; injury", "Bronchial injury", "injury; bronchus", "Injury of bronchus", "injury of bronchus", "Injury of bronchus (disorder)", "injury of bronchus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of bronchus", "shortest_name_length": 16}
{"curie": "UMLS:C0742007", "names": ["Catheter sepsis", "catheter sepsis", "CATHETER SEPSIS", "catheter (other); sepsis", "sepsis; catheter (other)", "Catheter related septicemia", "Catheter related septicaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Catheter related septicaemia", "shortest_name_length": 15}
{"curie": "UMLS:C2986678", "names": ["Stage II Childhood Non-Hodgkin Lymphoma", "stage II childhood non-Hodgkin lymphoma", "Ann Arbor Stage II Childhood Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage II Childhood Non-Hodgkin Lymphoma", "shortest_name_length": 39}
{"curie": "MONDO:0023554", "names": ["Acquired Testicular Failure", "Acquired testicular failure", "acquired testicular failure", "Acquired testicular failure (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired testicular failure", "shortest_name_length": 27}
{"curie": "UMLS:C0003834", "names": ["artery; insufficiency", "Arterial Insufficiency", "Arterial insufficiency", "ARTERIAL INSUFFICIENCY", "arterial insufficiency", "insufficiency; arterial", "arterial insufficiencies", "Arterial insufficiency (disorder)", "arterial insufficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arterial insufficiency", "shortest_name_length": 21}
{"curie": "MONDO:0003513", "names": ["stomach teratoma", "Gastric Teratoma", "gastric teratoma", "teratoma of stomach", "Teratoma of Stomach", "teratoma of the stomach", "Teratoma of the Stomach"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric teratoma", "shortest_name_length": 16}
{"curie": "UMLS:C0277525", "names": ["flu stomach", "Stomach flu", "Stomach Flu", "Gastric flu", "stomach flu", "Gastric Flu", "gastric flu", "Septic gastroenteritis", "Infective gastroenteritis", "Infectious gastroenteritis", "infectious gastroenteritis", "Septic gastroenteritis, NOS", "infectious; gastroenteritis", "gastroenteritis; infectious", "Infectious gastroenteritis NOS", "Infectious gastroenteritis, NOS", "Infectious gastroenteritis (disorder)", "infectious gastroenteritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infectious gastroenteritis", "shortest_name_length": 11}
{"curie": "MONDO:0005729", "names": ["Dicroceliasis", "Dicroceliosis", "dicroceliasis", "dicrocoeliasis", "Dicrocoeliasis", "Dicrocoeliases", "Dicrocoeliosis", "lancet; fluke disease", "fluke disease; lancet", "Lancet fluke infection", "infection; lancet fluke", "lancet fluke; infection", "Dicrocoeliasis (disorder)", "disease due to Dicrocoeliidae", "Disease due to Dicrocoeliidae", "DISEASES DUE TO DICROCOELIIDAE", "Dicrocoelium infectious disease", "Dicrocoelium disease or disorder", "Disease caused by Dicrocoeliidae", "Dicrocoelium caused disease or disorder", "Disease caused by Dicrocoeliidae (disorder)", "Infection caused by Dicrocoelium dendriticum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dicrocoeliasis", "shortest_name_length": 13}
{"curie": "UMLS:C1333560", "names": ["FIGO Stage IVA GTT", "FIGO Stage IVA Gestational Trophoblastic Tumor", "FIGO Stage IVA Gestational Trophoblastic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Stage IVA Gestational Trophoblastic Tumor", "shortest_name_length": 18}
{"curie": "UMLS:C3900103", "names": ["Favorable Prognosis Hodgkin Lymphoma", "Adult Favorable Prognosis Hodgkin Lymphoma", "adult favorable prognosis Hodgkin lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Favorable Prognosis Hodgkin Lymphoma", "shortest_name_length": 36}
{"curie": "MONDO:0006871", "names": ["Non-gestational Choriocarcinoma", "non-gestational choriocarcinoma", "Non gestational Choriocarcinoma", "Choriocarcinoma, Non gestational", "Non-gestational Choriocarcinomas", "Choriocarcinoma, Non-gestational", "Choriocarcinomas, Non-gestational"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-gestational choriocarcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0007710", "names": ["PHA", "HFA", "Romberg", "Parry-Romberg", "romberg disease", "ROMBERG DISEASE", "Romberg Disease", "Rombergs Disease", "Disease, Romberg", "Romberg syndrome", "hemiatrophy; face", "Romberg's Disease", "face; hemiatrophy", "romberg's disease", "Facial Hemiatrophy", "hemifacial atrophy", "Disease, Romberg's", "facial hemiatrophy", "Romberg's syndrome", "Hemifacial atrophy", "Hemifacial Atrophy", "Facial hemiatrophy", "Atrophy, Hemifacial", "hemifacial; atrophy", "Hemiatrophy, Facial", "atrophy; hemifacial", "Hemifacial Atrophies", "Facial Hemiatrophies", "Parry-Romberg Disease", "Hemiatrophies, Facial", "Parry Romberg Disease", "parry-romberg disease", "Facial trophoneurosis", "Atrophies, Hemifacial", "Parry-Romberg Syndrome", "parry-romberg syndrome", "PARRY-ROMBERG SYNDROME", "Parry-Romberg syndrome", "parry romberg syndrome", "Disease, Parry-Romberg", "Parry Romberg Syndrome", "Parry Romberg syndrome", "parry-Romberg syndrome", "Parry-Romberg's disease", "Syndrome, Parry-Romberg", "Atrophy of half of face", "parry rombergs syndrome", "Romberg's trophoneurosis", "Romberg Facial Hemiatrophy", "hemifacial atrophy romberg", "Romberg Hemi-Facial Atrophy", "Romberg hemi-facial atrophy", "Romberg Hemi Facial Atrophy", "Atrophy, Romberg Hemi-Facial", "atrophy; hemifacial, Romberg", "ATROPHY, HEMIFACIAL, ROMBERG", "hemifacial; atrophy, Romberg", "Hemi-Facial Atrophy, Romberg", "Facial Hemiatrophy of Romberg", "Facial hemiatrophy (disorder)", "progressive facial hemiatrophy", "FACE, HEMIATROPHY, PROGRESSIVE", "Progressive Facial Hemiatrophy", "Progressive facial hemiatrophy", "progressive hemifacial atrophy", "Progressive Hemifacial Atrophy", "Progressive hemifacial atrophy", "Atrophy, Progressive Hemifacial", "HEMIFACIAL ATROPHY, PROGRESSIVE", "Hemiatrophy, Progressive Facial", "hemifacial atrophy, progressive", "Facial Hemiatrophy, Progressive", "Hemifacial Atrophy, Progressive", "Atrophy of one side of the face", "Progressive Hemifacial Atrophies", "Progressive Facial Hemiatrophies", "Atrophies, Progressive Hemifacial", "Hemiatrophies, Progressive Facial", "Facial Hemiatrophies, Progressive", "Parry-Romberg syndrome (diagnosis)", "Progressive hemifacial atrophy (disorder)", "neuromuscular diseases Parry-Romberg syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "facial hemiatrophy", "shortest_name_length": 3}
{"curie": "UMLS:C0677721", "names": ["Mantle cell lymphoma stage IV", "stage IV mantle cell lymphoma", "Mantle Cell Lymphoma Stage IV", "mantle cell lymphoma stage IV", "Stage IV Mantle Cell Lymphoma", "metastatic mantle cell lymphoma", "Ann Arbor Stage IV Mantle Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mantle cell lymphoma stage IV", "shortest_name_length": 29}
{"curie": "UMLS:C4553244", "names": ["Stage II Thyroid Gland Medullary Cancer", "Stage II Thyroid Gland Medullary Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Thyroid Gland Medullary Carcinoma AJCC v8", "shortest_name_length": 39}
{"curie": "MONDO:0006946", "names": ["ROD", "CKD-MBD", "renal rickets", "Renal Rickets", "Renal rickets", "rickets, renal", "RICKETS, RENAL", "Renal, rickets", "renal; rickets", "rickets; renal", "Rickets, Renal", "renal disease bone", "renal bone disease", "Renal bone disease", "Renal osteodystrophy", "osteodystrophy renal", "OSTEODYSTROPHY RENAL", "renal osteodystrophy", "Renal Osteodystrophy", "osteodystrophy, renal", "OSTEODYSTROPHY, RENAL", "osteodystrophy; renal", "renal; osteodystrophy", "Osteodystrophy, Renal", "Renal Osteodystrophies", "renal Osteodystrophies", "Osteodystrophies, renal", "Osteodystrophies, Renal", "renal rickets (diagnosis)", "ROD - Renal osteodystrophy", "OSTEODYSTROPHY, PANNEPHRITIC", "Renal osteodystrophy (disorder)", "renal osteodystrophy (diagnosis)", "Chronic kidney disease-mineral and bone disorder", "Chronic Kidney Disease Mineral and Bone Disorder", "Chronic Kidney Disease-Mineral and Bone Disorder", "Chronic kidney disease mineral and bone disorder", "CKD-MBD - chronic kidney disease mineral and bone disorder", "Chronic kidney disease mineral and bone disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal osteodystrophy", "shortest_name_length": 3}
{"curie": "UMLS:C5419761", "names": ["Unresectable Paranasal Sinus Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Paranasal Sinus Squamous Cell Carcinoma", "shortest_name_length": 52}
{"curie": "MONDO:0054699", "names": ["PRAAS3", "PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 3", "proteasome-associated autoinflammatory syndrome 3", "PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 3, DIGENIC", "proteasome-associated autoinflammatory syndrome 3, digenic", "proteasome-associated autoinflammatory syndrome 3 and digenic forms"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "proteasome-associated autoinflammatory syndrome 3", "shortest_name_length": 6}
{"curie": "MONDO:0030448", "names": ["IMD86", "immunodeficiency 86", "IMMUNODEFICIENCY 86", "IMMUNODEFICIENCY 86, MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 86", "shortest_name_length": 5}
{"curie": "MONDO:0008792", "names": ["Familial angiolipomatosis", "familial angiolipomatosis", "angiolipomatosis, familial", "ANGIOLIPOMATOSIS, FAMILIAL", "Angiolipomatosis, Familial", "angiolipoma Microthromboticum", "Angiolipoma Microthromboticum", "ANGIOLIPOMA MICROTHROMBOTICUM", "Familial angiolipomatosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial angiolipomatosis", "shortest_name_length": 25}
{"curie": "MONDO:0002694", "names": ["thrombosis; cavernous", "cavernous; thrombosis", "Cavernous sinus thrombosis", "thrombosis cavernous sinus", "cavernous sinus thrombosis", "Cavernous Sinus Thromboses", "Cavernous Sinus Thrombosis", "sinus cavernous thrombosis", "Sinus Thromboses, Cavernous", "Sinus Thrombosis, Cavernous", "THROMBOSIS, CAVERNOUS SINUS", "Thrombosis, Cavernous Sinus", "Thromboses, Cavernous Sinus", "thrombosis of cavernous sinus", "Thrombosis of cavernous venous sinus", "thrombosis of cavernous venous sinus", "thrombosis of cavernous sinus (diagnosis)", "Cerebral venous thrombosis of cavernous sinus", "Thrombosis of cavernous venous sinus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cavernous sinus thrombosis", "shortest_name_length": 21}
{"curie": "MONDO:0011660", "names": ["DFNA22", "DFNA 22", "autosomal dominant deafness 22", "Deafness, Autosomal Dominant 22", "deafness, autosomal dominant 22", "DEAFNESS, AUTOSOMAL DOMINANT 22", "deafness, autosomal dominant type 22", "autosomal dominant nonsyndromic deafness 22", "MYO6 autosomal dominant nonsyndromic deafness", "autosomal dominant nonsyndromic hearing loss 22", "autosomal dominant nonsyndromic deafness type 22", "deafness, autosomal dominant nonsyndromic sensorineural 22", "Deafness, autosomal dominant nonsyndromic sensorineural 22", "DEAFNESS, AUTOSOMAL DOMINANT 22, WITH HYPERTROPHIC CARDIOMYOPATHY", "deafness, autosomal dominant 22, with hypertrophic cardiomyopathy", "autosomal dominant nonsyndromic deafness caused by mutation in MYO6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 22", "shortest_name_length": 6}
{"curie": "OMIM:617995", "names": ["IMPDH2V", "IMPDH2 ENZYME ACTIVITY, VARIATION IN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 7}
{"curie": "MONDO:0015930", "names": ["respiratory malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "respiratory malformation", "shortest_name_length": 24}
{"curie": "MONDO:0019633", "names": ["FEVER, FAMINE", "Recurrent fever", "Fever;relapsing", "Relapsing Fever", "fever recurrent", "Relapsing fever", "RELAPSING FEVER", "recurrent fever", "fever relapsing", "relapsing fever", "relapsing; fever", "Relapsing fevers", "relapsing fevers", "Fever, Relapsing", "fever; relapsing", "RELAPSING FEVERS", "fevers recurrent", "Relapsing Fevers", "Relapsing fever, NOS", "Recurrent fever, NOS", "Relapsing fever (disorder)", "relapsing fever (diagnosis)", "Unspecified relapsing fever", "Relapsing fever, unspecified", "Relapsing fever due to Borrelia", "Recurrent fever due to Borrelia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "relapsing fever", "shortest_name_length": 13}
{"curie": "MONDO:0007370", "names": ["Coracoclavicular Joint, Anomalous", "CORACOCLAVICULAR JOINT, ANOMALOUS", "coracoclavicular joint, anomalous"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coracoclavicular joint, anomalous", "shortest_name_length": 33}
{"curie": "MONDO:0018256", "names": ["AML with t(8;16)(p11;p13) translocation", "Acute myeloid leukemia with t(8;16)(p11;p13) translocation", "acute myeloid leukemia with t(8;16)(p11;p13) translocation", "Acute myeloid leukaemia with t(8;16)(p11;p13) translocation", "leukemia myelogenous acute (AML) with t(8;16)(p11;p13) translocation", "Acute myeloid leukemia with t(8;16)(p11;p13) translocation (disorder)", "Acute myeloid leukemia with t(8;16)(p11;p13) translocation (diagnosis)", "Acute myeloid leukemia with t(8;16)(p11;p13) translocation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia with t(8;16)(p11;p13) translocation", "shortest_name_length": 39}
{"curie": "UMLS:C1333513", "names": ["Extraosseous Ameloblastoma", "Extraosseous/Peripheral Ameloblastoma", "Ameloblastoma, Extraosseous/Peripheral Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extraosseous/Peripheral Ameloblastoma", "shortest_name_length": 26}
{"curie": "MONDO:0001217", "names": ["pseudomembranous conjunctivitis", "Pseudomembranous conjunctivitis", "Pseudomembranous Conjunctivitis", "conjunctivitis with pseudomembrane", "Pseudomembranous conjunctivitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudomembranous conjunctivitis", "shortest_name_length": 31}
{"curie": "MONDO:0037939", "names": ["porphyria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "porphyria", "shortest_name_length": 9}
{"curie": "UMLS:C4725000", "names": ["DLBCL, NOS Genetic Subtypes", "DLBCL, NOS Molecular Subtypes", "Diffuse Large B-Cell Lymphoma, Not Otherwise Specified Genetic Subtypes", "Diffuse Large B-Cell Lymphoma, Not Otherwise Specified Molecular Subtypes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse Large B-Cell Lymphoma, Not Otherwise Specified Molecular Subtypes", "shortest_name_length": 27}
{"curie": "MONDO:0012744", "names": ["LVNC9", "CMD1Y", "dilated cardiomyopathy 1Y", "CARDIOMYOPATHY, DILATED, 1Y", "cardiomyopathy, dilated, 1Y", "Cardiomyopathy, Dilated, 1y", "dilated cardiomyopathy type 1Y", "left ventricular noncompaction 9", "cardiomyopathy, dilated, type 1Y", "LEFT VENTRICULAR NONCOMPACTION 9", "TPM1 familial isolated dilated cardiomyopathy", "familial isolated dilated cardiomyopathy caused by mutation in TPM1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1Y", "shortest_name_length": 5}
{"curie": "UMLS:C3272483", "names": ["Ampulla of Vater EC Cell Serotonin-Producing NET", "Ampulla of Vater EC-Cell Serotonin-Producing Neuroendocrine Tumor", "Ampulla of Vater Enterochromaffin Cell Serotonin-Producing Neuroendocrine Tumor", "Enterochromaffin Cell Serotonin-Producing Neuroendocrine Tumor of the Ampullary Region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ampulla of Vater Enterochromaffin Cell Serotonin-Producing Neuroendocrine Tumor", "shortest_name_length": 48}
{"curie": "MONDO:0009563", "names": ["MSU", "msu", "msud", "MSUD", "MSUD2", "MSUD1B", "MSUD1A", "Ketoacidemia", "ketoacidemia", "Classic MSUD", "Ketoacidaemia", "BCKD Deficiency", "BCKD deficiency", "BCKD DEFICIENCY", "BCKDH deficiency", "Intermittent MSUD", "Intermediate MSUD", "Maple syrup disease", "maple syrup disease", "Classic BCKD deficiency", "BRANCHED-CHAIN KETONURIA", "Thiamine-responsive MSUD", "maple syrup urine disease", "maple-syrup-urine disease", "Maple-syrup-urine disease", "MAPLE SYRUP URINE DISEASE", "Maple Syrup Urine Disease", "Maple syrup urine disease", "disease maple syrup urine", "disease; maple-syrup-urine", "maple-syrup-urine; disease", "maple-syrup-urine; syndrome", "Branched-chain ketoaciduria", "branched chain ketoaciduria", "BRANCHED-CHAIN KETOACIDURIA", "Branched-Chain Ketoaciduria", "Branched chain ketoaciduria", "syndrome; maple-syrup-urine", "branched-chain ketoaciduria", "Branched Chain Ketoaciduria", "Ketoaciduria, Branched-Chain", "Intermittent BCKD deficiency", "Branched-Chain Ketoacidurias", "Intermediate BCKD deficiency", "Ketoacidurias, Branched-Chain", "Maple syrup urine disease, NOS", "MSUD (maple syrup urine disease)", "MSUD - Maple syrup urine disease", "MSUD (Maple Syrup Urine Disease)", "maple syrup urine disease type II", "Classic maple syrup urine disease", "Maple syrup urine disease, type 2", "Oxo-acid decarboxylase deficiency", "maple syrup urine disease, type 2", "Classic Maple Syrup Urine Disease", "Ketoacid decarboxylase deficiency", "MAPLE SYRUP URINE DISEASE, TYPE IB", "Maple syrup urine disease, type 1B", "maple syrup urine disease, type 1A", "maple syrup urine disease, classic", "MAPLE SYRUP URINE DISEASE, CLASSIC", "Keto acid decarboxylase deficiency", "Maple Syrup Urine Disease, Type II", "maple syrup urine disease, type IA", "MAPLE SYRUP URINE DISEASE, TYPE IA", "Maple Syrup Urine Disease, Type IA", "Maple Syrup Urine Disease, Classic", "Maple Syrup Urine Disease, Type IB", "MAPLE SYRUP URINE DISEASE, TYPE II", "maple syrup urine disease, type IB", "maple syrup urine disease, type 1B", "KETO ACID DECARBOXYLASE DEFICIENCY", "Keto Acid Decarboxylase Deficiency", "maple syrup urine disease, type II", "Classical maple syrup urine disease", "Classical Maple Syrup Urine Disease", "Thiamine-responsive BCKD deficiency", "Classic branched-chain ketoaciduria", "Maple Syrup Urine Disease, Classical", "Maple syrup urine disease (disorder)", "maple syrup urine disease (diagnosis)", "Intermittent Maple Syrup Urine Disease", "Intermittent maple syrup urine disease", "Intermediate Maple Syrup Urine Disease", "Intermediate maple syrup urine disease", "maple syrup urine disease, intermittent", "Maple Syrup Urine Disease, Intermittent", "MAPLE SYRUP URINE DISEASE, INTERMITTENT", "Maple Syrup Urine Disease, Intermediate", "MAPLE SYRUP URINE DISEASE, INTERMEDIATE", "Maple syrup urine disease, classic form", "maple syrup urine disease, Intermediate", "disease (or disorder); maple-syrup-urine", "Intermittent branched chain ketoaciduria", "Intermediate branched chain ketoaciduria", "Intermittent branched-chain ketoaciduria", "dihydrolipoamide dehydrogenase deficiency", "Thiamin-responsive maple syrup urine disease", "Maple syrup urine disease, intermittent form", "Thiamine-responsive maple syrup urine disease", "Thiamine Responsive Maple Syrup Urine Disease", "maple syrup urine disease type II (diagnosis)", "MAPLE SYRUP URINE DISEASE, THIAMINE-RESPONSIVE", "Classical maple syrup urine disease (disorder)", "maple syrup urine disease, thiamine-responsive", "Maple Syrup Urine Disease, Thiamine Responsive", "Maple Syrup Urine Disease, Thiamine-Responsive", "Branched chain ketoacid dehydrogenase deficiency", "Intermittent maple syrup urine disease (disorder)", "Intermediate maple syrup urine disease (disorder)", "branched-chain 2-ketoacid dehydrogenase deficiency", "Branched-chain 2-ketoacid dehydrogenase deficiency", "Maple syrup urine disease, thiamine-responsive form", "Branched-Chain alpha-Keto Acid Dehydrogenase Deficiency", "Severe branched chain ketoacid dehydrogenase deficiency", "Branched Chain alpha Keto Acid Dehydrogenase Deficiency", "Thiamin-responsive maple syrup urine disease (disorder)", "branched-chain Alpha-Keto acid dehydrogenase deficiency", "BRANCHED-CHAIN ALPHA-KETO ACID DEHYDROGENASE DEFICIENCY", "Branched-chain alpha-keto acid dehydrogenase deficiency", "Partial branched chain ketoacid dehydrogenase deficiency", "BCKD - Branched chain alpha-ketoacid dehydrogenase deficiency", "Classic branched-chain alpha-ketoacid dehydrogenase deficiency", "Intermittent branched-chain alpha-ketoacid dehydrogenase deficiency", "Intermediate branched-chain alpha-ketoacid dehydrogenase deficiency", "Thiamine-responsive branched-chain alpha-ketoacid dehydrogenase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maple syrup urine disease", "shortest_name_length": 3}
{"curie": "UMLS:C5420035", "names": ["Sinonasal Large Cell Neuroendocrine Carcinoma", "Nasal Cavity and Paranasal Sinus Large Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Large Cell Neuroendocrine Carcinoma", "shortest_name_length": 45}
{"curie": "MONDO:0006650", "names": ["beck syndrome", "BECK SYNDROME", "becks syndrome", "Beck's syndrome", "beck's syndrome", "anterior cord syndrome", "Anterior cord syndrome", "cord syndrome anterior", "Ventral medullary syndrome", "ANTERIOR SPINAL ARTERY SYNDROME", "Anterior Spinal Artery Syndrome", "anterior spinal artery syndrome", "Anterior spinal artery syndrome", "syndrome; anterior spinal artery", "Syndrome, Anterior Spinal Artery", "Anterior cord syndrome (disorder)", "anterior cord syndrome (diagnosis)", "anterior spinal artery syndromic disease", "Anterior spinal artery occlusion syndrome", "syndromic disease of anterior spinal artery"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anterior spinal artery syndrome", "shortest_name_length": 13}
{"curie": "UMLS:C1334299", "names": ["Jugular Foramen Tumor", "Jugular Foramen Tumors", "Tumor of Jugular Foramen", "Jugular Foramen Neoplasm", "Jugular Foramen Neoplasms", "Neoplasm of Jugular Foramen", "Tumor of the Jugular Foramen", "Neoplasm of the Jugular Foramen"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jugular Foramen Neoplasm", "shortest_name_length": 21}
{"curie": "MONDO:0012366", "names": ["GBD3", "Gallbladder Disease 3", "gallbladder disease 3", "GALLBLADDER DISEASE 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gallbladder disease 3", "shortest_name_length": 4}
{"curie": "MONDO:0005115", "names": ["tle", "TLE", "FTLE", "Psychomotor seizure", "SEIZURE PSYCHOMOTOR", "psychomotor seizure", "psychomotor seizures", "Psychomotor seizures", "SEIZURE TEMPORAL LOBE", "lobe temporal seizure", "temporal lobe seizure", "lobe seizures temporal", "PSYCHOMOTOR EQUIVALENT", "seizures temporal lobe", "temporal lobe epilepsy", "CONVULSION PSYCHOMOTOR", "Temporal lobe seizures", "EPILEPSY TEMPORAL LOBE", "Epilepsy;temporal lobe", "Epilepsy temporal lobe", "Convulsion psychomotor", "Temporal lobe epilepsy", "epilepsy lobe temporal", "Temporal Lobe Epilepsy", "CONVULSION, PSYCHOMOTOR", "epilepsy, temporal lobe", "epilepsy; temporal lobe", "Epilepsy, temporal lobe", "EPILEPSY, TEMPORAL LOBE", "Epilepsy, Temporal Lobe", "Seizures, temporal lobe", "psychomotor; convulsions", "Temporal Lobe Epilepsies", "convulsions; psychomotor", "temporal lobe; epileptic", "Epilepsies, Temporal Lobe", "epilepsy of temporal lobe", "Temporal epilepsy, familial", "TLE - Temporal lobe epilepsy", "Psychomotor seizure (finding)", "SEIZURE DISORDER TEMPORAL LOBE", "Familial temporal lobe epilepsy", "Temporal lobe epilepsy syndrome", "disorder temporal lobe epilepsy", "temporal lobe epilepsy familial", "Epilepsy, familial temporal lobe", "epilepsy, familial temporal lobe", "Temporal lobe epilepsy (disorder)", "temporal lobe epilepsy (diagnosis)", "Familial temporal lobe epilepsy (disorder)", "Familial temporal lobe epilepsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "temporal lobe epilepsy", "shortest_name_length": 3}
{"curie": "UMLS:C2987140", "names": ["Pancreatic Moderately Differentiated Ductal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Moderately Differentiated Ductal Adenocarcinoma", "shortest_name_length": 58}
{"curie": "MONDO:0010193", "names": ["WSS", "WVS", "Weaver", "WEAVER SYNDROME", "weaver syndrome", "Weaver syndrome", "syndrome weaver", "WEAVER syndrome", "Weaver Syndrome", "syndrome weavers", "weaver's syndrome", "Weaver's syndrome", "Weaver-like syndrome", "Weaver like syndrome", "Weaver-Like Syndrome", "WEAVER-LIKE SYNDROME", "WEAVER-like syndrome", "Weaver Smith syndrome", "weaver-smith syndrome", "Weaver-Smith Syndrome", "WEAVER-SMITH SYNDROME", "Weaver-Smith syndrome", "EZH2 related overgrowth", "Weaver Williams syndrome", "Weaver-Williams syndrome", "Weaver syndrome (disorder)", "Weaver-Smith syndrome (WSS)", "Marshall-Smith-Weaver syndrome", "camptodactyly - overgrowth - unusual facies", "Camptodactyly-overgrowth-unusual facies syndrome", "camptodactyly-overgrowth-unusual facies syndrome", "overgrowth syndrome with accelerated skeletal maturation, unusual facies, and camptodactyly", "mental retardation, microcephaly, weight deficiency, unusual facies, clinodactyly, bone hypoplasia, and cleft palate", "intellectual disability, microcephaly, weight deficiency, unusual facies, clinodactyly, bone hypoplasia, and cleft palate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Weaver syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0010599", "names": ["Congenital cerebral granulomas", "congenital cerebral granulomas", "Granulomas, congenital cerebral", "granulomas, congenital cerebral", "GRANULOMAS, CONGENITAL CEREBRAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "granulomas, congenital cerebral", "shortest_name_length": 30}
{"curie": "UMLS:C5668273", "names": ["Pleural Calcifying Fibrous Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pleural Calcifying Fibrous Tumor", "shortest_name_length": 32}
{"curie": "MONDO:0032846", "names": ["OI20", "osteogenesis imperfecta type 20", "osteogenesis imperfecta type XX", "osteogenesis imperfecta, type 20", "OSTEOGENESIS IMPERFECTA, TYPE XX"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteogenesis imperfecta, type 20", "shortest_name_length": 4}
{"curie": "MONDO:0014850", "names": ["RPEM", "RETINITIS PIGMENTOSA AND ERYTHROCYTIC MICROCYTOSIS", "retinitis pigmentosa and erythrocytic microcytosis", "retinitis pigmentosa and erythrocytic microcytosis; RPEM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa and erythrocytic microcytosis", "shortest_name_length": 4}
{"curie": "UMLS:C0264110", "names": ["apophysitis", "Apophysitis", "Apophysitis NOS", "Apophysitis, NOS", "Juvenile apophysitis", "Apophysitis (disorder)", "Apophysitis not specified as adult or juvenile, of unspecified site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Apophysitis", "shortest_name_length": 11}
{"curie": "MONDO:0001325", "names": ["Ca penis", "Penile Ca", "penile Ca", "PENIS CANCER", "Penis Cancer", "penis cancer", "cancer penis", "Penis Cancers", "Cancer, Penis", "penile cancer", "Penis--Cancer", "cancer penile", "Penile Cancer", "Penile cancer", "Cancers, Penis", "penile cancers", "Penile Cancers", "Cancer, Penile", "penile neoplasm", "Cancers, Penile", "of penis cancer", "Cancer of penis", "cancer of penis", "Cancer of Penis", "cancer of the penis", "Cancer of the Penis", "CA - Cancer of penis", "Malignant Penile Tumor", "malignant penile tumor", "Malignant penile tumor", "malignant Penile tumor", "Cancer of body of penis", "Malignant tumor of penis", "malignant tumor of penis", "Malignant Tumor of Penis", "malignant penis neoplasm", "Malignant Penile Neoplasm", "Malignant tumour of penis", "Penile malignant neoplasm", "malignant penile neoplasm", "Penile neoplasms malignant", "malignant neoplasm of penis", "Malignant Neoplasm of Penis", "Malignant neoplasm of penis", "Malignant Tumor of the Penis", "malignant tumor of the penis", "Penile malignant neoplasm NOS", "malignant neoplasm of the penis", "Malignant Neoplasm of the Penis", "Malignant tumor of body of penis", "Malignant neoplasm of penis, NOS", "Malignant tumour of body of penis", "Malignant tumor of shaft of penis", "Malignant tumour of shaft of penis", "Malignant tumor of penis (disorder)", "Malignant neoplasm of body of penis", "malignant neoplasm of body of penis", "penile neoplasm malignant body of penis", "malignant neoplasm of penis (diagnosis)", "Malignant neoplasm of penis, unspecified", "Malignant tumor of body of penis (disorder)", "Malignant neoplasm of penis, part unspecified", "malignant neoplasm of body of penis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "penile cancer", "shortest_name_length": 8}
{"curie": "UMLS:C5667237", "names": ["Relapsed Metastatic Melanoma", "Recurrent Metastatic Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Metastatic Melanoma", "shortest_name_length": 28}
{"curie": "MONDO:0012677", "names": ["ATFB4", "atrial fibrillation familial 4", "Atrial Fibrillation, Familial, 4", "atrial fibrillation, familial, 4", "ATRIAL FIBRILLATION, FAMILIAL, 4", "KCNE2 familial atrial fibrillation", "atrial fibrillation, familial, type 4", "atrial fibrillation familial 4 (diagnosis)", "familial atrial fibrillation caused by mutation in KCNE2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial fibrillation, familial, 4", "shortest_name_length": 5}
{"curie": "MONDO:0013243", "names": ["HMN2C", "HMN 2C", "DHMN2C", "HMN IIC", "HSPB3 neuronopathy, distal hereditary motor", "distal hereditary motor neuropathy type IIC", "distal hereditary motor neuronopathy type 2C", "neuropathy, distal hereditary motor, type 2C", "NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC", "neuronopathy, distal hereditary motor, type 2C", "neuronopathy, distal hereditary motor, type IIC", "NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC", "neuronopathy, distal hereditary motor caused by mutation in HSPB3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuronopathy, distal hereditary motor, type 2C", "shortest_name_length": 5}
{"curie": "UMLS:C5420498", "names": ["Metastatic Differentiated Thyroid Gland Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Differentiated Thyroid Gland Carcinoma", "shortest_name_length": 49}
{"curie": "MONDO:0020796", "names": ["SRS1", "SILVER-RUSSELL SYNDROME 1", "Silver-Russell syndrome 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Silver-Russell syndrome 1", "shortest_name_length": 4}
{"curie": "UMLS:C5238507", "names": ["Locally Advanced Epithelioid Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Epithelioid Sarcoma", "shortest_name_length": 36}
{"curie": "MONDO:0014401", "names": ["ECDM", "Miura type epiphyseal chondrodysplasia", "epiphyseal chondrodysplasia, MIURA type", "EPIPHYSEAL CHONDRODYSPLASIA, MIURA TYPE", "tall stature-scoliosis-macrodactyly of the halluces syndrome", "tall stature-scoliosis-macrodactyly of the great toes syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tall stature-scoliosis-macrodactyly of the great toes syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0020176", "names": ["palpebral sebaceous gland tumor", "sebaceous gland of eyelid tumor", "sebaceous gland of eyelid neoplasm", "tumor of sebaceous gland of eyelid", "neoplasm of sebaceous gland of eyelid", "sebaceous gland of eyelid neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "palpebral sebaceous gland tumor", "shortest_name_length": 31}
{"curie": "MONDO:0043653", "names": ["coldsore", "Cold Sore", "Cold sore", "cold sore", "COLD SORE", "Fever sore", "fever sore", "cold sores", "Cold Sores", "Sore, cold", "FEVER SORE", "herpes lip", "lip herpes", "Sore, Cold", "Cold sores", "fever sores", "herpes; lip", "herpes lips", "Sores, cold", "lip; herpes", "Sores, Cold", "Fever Blister", "Fever blister", "lip cold sore", "blister fever", "Herpes on lip", "herpes on lip", "FEVER BLISTER", "fever blister", "blister, fever", "lip cold sores", "Fever Blisters", "Blister, Fever", "fever blisters", "Cold sores lip", "HERPES LABIALIS", "herpes labialis", "herpes febrilis", "Herpes Labialis", "Blisters, Fever", "Herpes labialis", "blisters, fever", "febrilis; herpes", "herpes; febrilis", "herpes; labialis", "labialis; herpes", "Cold sore (herpetic)", "Labial Herpes Simplex", "labial Herpes simplex", "Herpes Simplex, Labial", "Herpes simplex, labial", "herpes simplex labialis", "Herpes simplex labialis", "Herpes labialis (disorder)", "herpes simplex labialis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "herpes labialis", "shortest_name_length": 8}
{"curie": "MONDO:0002653", "names": ["penis Paget disease", "penis adenocarcinoma", "Penile Paget Disease", "disease paget's penis", "penis Paget's disease", "penile adenocarcinoma", "Penile adenocarcinoma", "adenocarcinoma of penis", "Paget's Disease of Penis", "Paget's disease of penis", "Paget Disease of the Penis", "Paget disease of the penis", "adenocarcinoma of the penis", "Paget's disease of the penis", "Paget's Disease of the Penis", "penis mammary Paget's disease", "extramammary Paget's disease of penis", "extramammary Paget's disease of penis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paget disease of the penis", "shortest_name_length": 19}
{"curie": "UMLS:C5420190", "names": ["Laryngeal Inflammatory Myofibroblastic Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laryngeal Inflammatory Myofibroblastic Tumor", "shortest_name_length": 44}
{"curie": "MONDO:0018151", "names": ["CoQ Deficiency", "CoQ10 deficiency", "Ubiquinone Deficiency", "Coenzyme Q Deficiency", "coenzyme Q10 deficiency", "COENZYME Q10 DEFICIENCY", "Coenzyme Q10 Deficiency", "Coenzyme Q10 deficiency", "CoQ10 deficiency, primary", "Coq10 Deficiency, Primary", "coenzyme Q10 deficiency disease", "COENZYME Q10 DEFICIENCY, PRIMARY", "coenzyme Q10 deficiency, primary", "Coenzyme Q10 deficiency (disorder)", "Coenzyme Q10 deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coenzyme Q10 deficiency", "shortest_name_length": 14}
{"curie": "MONDO:0009713", "names": ["MYP18", "Myopia 18", "MYOPIA 18, AUTOSOMAL RECESSIVE", "Myopia 18, Autosomal Recessive", "myopia 18, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopia 18, autosomal recessive", "shortest_name_length": 5}
{"curie": "MONDO:0000283", "names": ["Korean hemorrhagic fever", "Hantavirus hemorrhagic fever with renal syndrome, Seoul virus type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hantavirus hemorrhagic fever with renal syndrome, Seoul virus type", "shortest_name_length": 24}
{"curie": "UMLS:C0280171", "names": ["intermediate-grade, stage IV adult NHL", "NHL, intermediate grade, stage IV adult", "adult NHL, stage IV, intermediate grade", "intermediate-grade, metastatic adult NHL", "NHL, intermediate grade, metastatic adult", "adult NHL, metastatic, intermediate grade", "Stage IV Intermediate Grade Adult Non-Hodgkin's Lymphoma", "adult non-Hodgkin's lymphoma, intermediate grade, stage IV", "lymphoma, intermediate grade, stage IV adult non-Hodgkin's", "non-Hodgkin's lymphoma, intermediate grade, stage IV adult", "intermediate-grade, metastatic adult non-Hodgkin's lymphoma", "adult non-Hodgkin's lymphoma, intermediate grade, metastatic", "non-Hodgkin's lymphoma, intermediate grade, metastatic adult", "lymphoma, intermediate grade, metastatic adult non-Hodgkin's"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Intermediate Grade Adult Non-Hodgkin's Lymphoma", "shortest_name_length": 38}
{"curie": "UMLS:C3887503", "names": ["Neonatal Listeriosis", "listeriosis; neonatal", "neonatal; listeriosis", "LISTERIOSIS IN NEWBORN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neonatal Listeriosis", "shortest_name_length": 20}
{"curie": "MONDO:0004409", "names": ["Nipple Duct Carcinoma", "nipple duct carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nipple duct carcinoma", "shortest_name_length": 21}
{"curie": "UMLS:C0442856", "names": ["hypoperfusion", "Hypoperfusion", "Hypoperfusion (qualifier value)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypoperfusion", "shortest_name_length": 13}
{"curie": "MONDO:0014487", "names": ["SIFD", "SIFD syndrome", "sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay", "SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS, AND DEVELOPMENTAL DELAY", "congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0000489", "names": ["diabetic encephalopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diabetic encephalopathy", "shortest_name_length": 23}
{"curie": "MONDO:0007245", "names": ["NF6", "Multiple birthmarks", "neurofibromatosis type 6", "Neurofibromatosis type 6", "Multiple café-au-lait spots", "familial café-au-lait spots", "familial cafe-au-lait spots", "multiple cafe-au-lait spots", "Multiple cafe-au-lait spots", "Familial café-au-lait spots", "multiple café-au-lait spots", "Cafe-au-Lait Spots, Multiple", "cafe au lait spots, multiple", "cafe-au-lait spots, multiple", "CAFE-AU-LAIT SPOTS, MULTIPLE", "Cafe au lait spots, multiple", "NF6 - neurofibromatosis type 6", "multiple cafe-au-lait syndrome", "multiple café-au-lait syndrome", "Multiple café-au-lait syndrome", "Neurofibromatosis type 6 (disorder)", "autosomal dominant café au lait spots", "Multiple flat light-brown marks on skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cafe au lait spots, multiple", "shortest_name_length": 3}
{"curie": "UMLS:C0581287", "names": ["Injection site redness", "Injection site erythema", "Erythema at injection site", "Injection site erythema (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Erythema at injection site", "shortest_name_length": 22}
{"curie": "MONDO:0015735", "names": ["severe congenital (neonatal) NM", "severe congenital nemaline myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe congenital nemaline myopathy", "shortest_name_length": 31}
{"curie": "MONDO:0017810", "names": ["Variant ABeta2M amyloidosis", "variant ABeta2M amyloidosis", "autosomal dominant beta2-microglobulinic amyloidosis", "Autosomal dominant beta2-microglobulinic amyloidosis", "Autosomal dominant beta2-microglobulinic amyloidosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "variant ABeta2M amyloidosis", "shortest_name_length": 27}
{"curie": "MONDO:0003282", "names": ["Cyst ovary", "ovary cyst", "CYST OVARY", "cyst; ovary", "ovary; cyst", "cystic ovary", "Cyst;ovarian", "OVARIAN CYST", "Cystic;ovary", "ovary cystic", "ovarian cyst", "Ovarian cyst", "Ovarian Cyst", "ovarian cysts", "cystic; ovary", "ovary; cystic", "Cyst of Ovary", "Ovarian cysts", "cyst, ovarian", "Cyst, Ovarian", "Ovarian Cysts", "Cyst of ovary", "cyst of ovary", "cystic ovaries", "Ovaries--Cysts", "cysts, ovarian", "Cystic ovaries", "Cysts, Ovarian", "Ovarian cyst NOS", "Cyst of the Ovary", "Ovarian cyst, NOS", "Cyst of ovary NOS", "corpus luteum cyst", "OVARIAN MASS CYSTIC", "ovarian cystic mass", "cystic ovarian mass", "corpus luteum cysts", "Ovarian cystic mass", "cyst, corpus luteum", "cysts, corpus luteum", "ovarian cyst (disease)", "Cyst of ovary (disorder)", "Unspecified ovarian cysts", "cyst of ovary (diagnosis)", "Ovarian cystic abnormality", "Ovarian retention cyst, NOS", "Other and unspecified ovarian cyst", "Cystic abnormalities of the ovaries", "Other and unspecified ovarian cysts", "Ovarian cyst benign (excl physiological)", "Ovarian cyst benign (excluding physiological)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian cyst", "shortest_name_length": 10}
{"curie": "MONDO:0060720", "names": ["CDGF", "congenital disorder of glycosylation with defective fucosylation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital disorder of glycosylation with defective fucosylation", "shortest_name_length": 4}
{"curie": "UMLS:C0280381", "names": ["nasopharynx lymphoepithelioma, stage II", "Nasopharyngeal lymphepithelioma stage II", "Nasopharyngeal lymphoepithelioma stage II", "Stage II Lymphoepithelioma of Nasopharynx", "Stage II Nasopharyngeal Lymphoepithelioma", "nasopharyngeal lymphoepithelioma, stage II", "Stage II Lymphoepithelioma of the Nasopharynx", "stage II lymphoepithelioma of the nasopharynx", "lymphoepithelioma of the nasopharynx, stage II", "Stage II Nasopharyngeal Undifferentiated Carcinoma", "Nasopharyngeal Undifferentiated Carcinoma Stage II", "Stage II Undifferentiated Nasopharyngeal Throat Cancer", "Stage II Nasopharyngeal Undifferentiated Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasopharyngeal lymphoepithelioma stage II", "shortest_name_length": 39}
{"curie": "UMLS:C0270686", "names": ["Cerebral fungus", "Cerebral mycosis", "fungal infection brain", "brain fungal infection", "brain fungal infections", "Fungal infection of brain", "Cerebral fungal infection", "fungal infection of brain", "Fungal infection of brain (disorder)", "fungal infection of brain (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fungal infection of brain", "shortest_name_length": 15}
{"curie": "MONDO:0000777", "names": ["gastrointestinal allergy", "digestive tract allergic disease", "allergic disease of digestive tract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastrointestinal allergy", "shortest_name_length": 24}
{"curie": "MONDO:0021468", "names": ["Benign Adrenal Medulla Tumor", "benign adrenal medulla tumor", "benign adrenal medulla neoplasm", "Benign tumor of adrenal medulla", "benign tumor of adrenal medulla", "Benign Adrenal Medulla Neoplasm", "adrenal medulla benign neoplasm", "Benign Tumor of Adrenal Medulla", "Benign tumour of adrenal medulla", "benign neoplasm of adrenal medulla", "Benign Neoplasm of Adrenal Medulla", "Benign neoplasm of adrenal medulla", "Benign Tumor of the Adrenal Medulla", "benign tumor of the adrenal medulla", "benign neoplasm of the adrenal medulla", "Benign Neoplasm of the Adrenal Medulla", "Benign neoplasm of adrenal medulla (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of adrenal medulla", "shortest_name_length": 28}
{"curie": "MONDO:0003277", "names": ["Ear tumor", "Ear Tumor", "Ear Cancer", "cancer ear", "Ear tumour", "ear cancer", "Ear--Tumors", "ear cancers", "Neoplasm;ear", "ear neoplasm", "Tumor of Ear", "Ear Neoplasm", "Ear neoplasm", "cancer of ear", "Cancer of Ear", "Neoplasm, Ear", "Ear Neoplasms", "Neoplasms, Ear", "Aural neoplasm", "Neoplasm of ear", "neoplasm of ear", "Neoplasm of Ear", "auricular cancer", "Tumor of the Ear", "Auricular Cancer", "Auricular Cancers", "Cancer of the Ear", "cancer of the ear", "Cancer, Auricular", "Ear Auricle Cancer", "Cancers, Auricular", "Neoplasm malig;ear", "Neoplasm of the ear", "Neoplasm of the Ear", "malignant Ear tumor", "neoplasm of the ear", "Ear Auricle Cancers", "Malignant Ear Tumor", "Cancer of Ear Auricle", "malignant ear neoplasm", "malignant Ear neoplasm", "Malignant Tumor of Ear", "Malignant Ear Neoplasm", "malignant tumor of ear", "Ear neoplasm malignant", "malignant tumor of Ear", "neoplasm of ear malignant", "malignant neoplasm of Ear", "Malignant neoplasm of ear", "Malignant Neoplasm of Ear", "malignant neoplasm of ear", "malignant tumor of the Ear", "Malignant Tumor of the Ear", "Neoplasm of ear (disorder)", "neoplasm of ear (diagnosis)", "malignant neoplasm of the Ear", "Malignant Neoplasm of the Ear", "malignant neosplasm of the ear", "Malignant neoplasm of ear (disorder)", "Malignant neoplasm of ear (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant ear neoplasm", "shortest_name_length": 9}
{"curie": "UMLS:C0012684", "names": ["Blastocyst Disintegration", "Disintegration, Blastocyst", "Disintegration of Blastocyst"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Blastocyst Disintegration", "shortest_name_length": 25}
{"curie": "UMLS:C5206446", "names": ["Stage IIA2 Cervical Cancer FIGO 2018", "Stage IIA2 Cervical Carcinoma FIGO 2018"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA2 Cervical Cancer FIGO 2018", "shortest_name_length": 36}
{"curie": "MONDO:0003778", "names": ["IEI", "hypoimmunity", "Immunodeficient", "immunodeficiency", "Immunodeficiency", "IMMUNODEFICIENCY", "Immune deficiency", "immune deficiency", "Deficiency;immune", "immunodeficiencies", "Immunodeficient NOS", "Immunodeficiency NOS", "Immunodeficiency, NOS", "IMMUNOLOGIC DEFICIENCY", "immunodeficiency disease", "Immunodeficiency disease", "primary immunodeficiency", "inborn error of immunity", "immunodeficiency disorder", "Decreased immune function", "inborn errors of immunity", "immunodeficiency syndrome", "Immunodeficiency Disorder", "Immunodeficiency disorder", "Immunodeficiency Syndrome", "immune deficiency disorder", "Immunodeficiency syndromes", "immunodeficiency syndromes", "immunodeficiency disorders", "antibody deficiency syndrome", "antibody deficiency syndromes", "Immunodeficiency, unspecified", "syndrome, antibody deficiency", "deficiency syndrome, antibody", "deficiency syndromes, antibody", "syndromes, antibody deficiency", "Unspecified immunity deficiency", "immunologic deficiency syndrome", "Immunologic Deficiency Syndrome", "Immunologic Deficiency Syndromes", "primary immunodeficiency disease", "Syndrome, Immunologic Deficiency", "syndrome, immunologic deficiency", "Deficiency Syndrome, Immunologic", "deficiency syndrome, immunologic", "syndromes, immunologic deficiency", "immunological deficiency syndrome", "Syndromes, Immunologic Deficiency", "Deficiency Syndromes, Immunologic", "Immunological Deficiency Syndrome", "deficiency syndromes, immunologic", "Syndrome, Immunological Deficiency", "Immunological Deficiency Syndromes", "Deficiency Syndrome, Immunological", "immunological deficiency syndromes", "Immunological deficiency syndromes", "syndrome, immunological deficiency", "deficiency syndrome, immunological", "deficiency syndromes, immunological", "Syndromes, Immunological Deficiency", "Deficiency Syndromes, Immunological", "syndromes, immunological deficiency", "Immunodeficiency disorder (disorder)", "immunodeficiency disorders (diagnosis)", "Immune deficiency disorder, disease or syndrome", "Immune Deficiency Disorders, Diseases and Syndromes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn error of immunity", "shortest_name_length": 3}
{"curie": "MONDO:0020072", "names": ["childhood epilepsy syndrome", "pediatric epilepsy syndrome", "epilepsy syndrome of childhood", "childhood-onset epilepsy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood-onset epilepsy syndrome", "shortest_name_length": 27}
{"curie": "UMLS:C3897762", "names": ["Recurrent Anaplastic Astrocytoma", "recurrent childhood anaplastic astrocytoma", "Recurrent Childhood Anaplastic Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Anaplastic Astrocytoma", "shortest_name_length": 32}
{"curie": "MONDO:0020352", "names": ["MSA-p", "MSA, parkinsonian type", "multiple system atrophy, parkinsonian type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple system atrophy, parkinsonian type", "shortest_name_length": 5}
{"curie": "UMLS:C0272891", "names": ["Sprain;knee", "sprain knee", "knee sprain", "KNEE SPRAIN", "Knee sprain", "knee sprains", "knees sprain", "knees sprains", "sprained knee", "knee sprained", "Sprain of knee", "Sprain of knee NOS", "Sprain of knee, NOS", "Sprain of knee joint", "knee sprain (diagnosis)", "Sprain of knee (disorder)", "Sprain of ligament of knee joint"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Knee sprain", "shortest_name_length": 11}
{"curie": "MONDO:0014215", "names": ["CILD27", "primary ciliary dyskinesia 27", "CILIARY DYSKINESIA, PRIMARY, 27", "ciliary dyskinesia, primary, 27", "CCDC65 primary ciliary dyskinesia", "primary ciliary dyskinesia type 27", "ciliary dyskinesia, primary, type 27", "primary ciliary dyskinesia 27 without situs inversus", "primary ciliary dyskinesia caused by mutation in CCDC65", "ciliary dyskinesia, primary, 27, without situs inversus", "CILIARY DYSKINESIA, PRIMARY, 27, WITHOUT SITUS INVERSUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia 27", "shortest_name_length": 6}
{"curie": "MONDO:0018020", "names": ["hydrargyria", "Hydrargyria", "Mercurialism", "mercurialism", "MERCURIALISM", "hydrargyrism", "Hydrargyrism", "Hydrargyrosis", "mercury poison", "mercury poisons", "Mercury toxicity", "poisoning mercury", "mercury poisoning", "Mercury poisoning", "Mercury Poisoning", "Poisoning, Mercury", "Mercury Poisonings", "Poisonings, Mercury", "Mercury intoxication", "poisoning by mercury", "Mercury poisoning syndrome", "Mercury compound poisoning", "Mercury causing toxic effect", "poisoning by mercury (diagnosis)", "Poisoning by compounds of mercury", "Toxic effect of mercury and its compounds", "Toxic effects of mercury and its compounds", "Toxic effects of mercury and its compounds NOS", "Toxic effect of mercury and its compounds, NOS", "Toxic effect of mercury and/or mercury compound", "Mercury or mercury compound causing toxic effect", "Toxic effect of mercury and/or mercury compound (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mercury poisoning", "shortest_name_length": 11}
{"curie": "MONDO:0002515", "names": ["Liver Disease", "HEPATOBILIARY DISEASE", "Hepatobiliary Disease", "Hepatobiliary disease", "hepatobiliary disease", "hepatobiliary disorder", "Hepatobiliary Disorder", "Hepatobiliary Diseases", "hepatobiliary disorders", "Hepatobiliary Disorders", "Hepatobiliary disorders", "hepatobiliary disease\"@e", "Liver and Biliary Disease", "liver and biliary disease", "Hepatobiliary disease NOS", "Liver and Biliary Disorder", "liver and biliary disorder", "hepatobiliary system disease", "liver and biliary tract disease", "disease of hepatobiliary system", "disorder of hepatobiliary system", "liver and biliary system disorder", "Liver and Biliary System Disorder", "LIVER AND BILIARY SYSTEM DISORDERS", "hepatobiliary disorders (diagnosis)", "DISEASES OF THE LIVER AND BILIARY SYSTEM", "hepatobiliary system disease or disorder", "disease or disorder of hepatobiliary system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatobiliary disorder", "shortest_name_length": 13}
{"curie": "MONDO:0021360", "names": ["Parathyroid tumor", "parathyroid tumor", "Parathyroid Tumor", "parathyroid tumors", "Parathyroid tumour", "tumor of parathyroid", "Parathyroid Neoplasm", "Tumor of Parathyroid", "parathyroid neoplasm", "Neoplasm, Parathyroid", "Parathyroid tumor NOS", "Parathyroid neoplasia", "neoplasms parathyroid", "Parathyroid Neoplasms", "Neoplasms, Parathyroid", "Parathyroid tumour NOS", "neoplasm of parathyroid", "Neoplasm of Parathyroid", "Parathyroid Gland Tumor", "parathyroid gland tumor", "tumor of the parathyroid", "Tumor of the Parathyroid", "Tumor of Parathyroid Gland", "tumor of parathyroid gland", "Parathyroid Gland Neoplasm", "parathyroid gland neoplasm", "Tumor of parathyroid gland", "Parathyroid glands--Tumors", "Neoplasm of the Parathyroid", "neoplasm of the parathyroid", "Tumour of parathyroid gland", "Neoplasm of parathyroid gland", "Neoplasm of Parathyroid Gland", "neoplasm of parathyroid gland", "tumor of the parathyroid gland", "Tumor of the Parathyroid Gland", "neoplasm of the parathyroid gland", "Neoplasm of the Parathyroid Gland", "Neoplasm of the parathyroid gland", "parathyroid gland neoplasm (disease)", "Neoplasm of parathyroid gland (disorder)", "neoplasm of parathyroid gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tumor of parathyroid gland", "shortest_name_length": 17}
{"curie": "UMLS:C5400205", "names": ["Discouragement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Discouragement", "shortest_name_length": 14}
{"curie": "UMLS:C4682626", "names": ["Stage IVA Ovarian Cancer", "Stage IVA Ovarian Cancer AJCC v8", "Stage IVA Ovarian Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Ovarian Cancer AJCC v8", "shortest_name_length": 24}
{"curie": "UMLS:C3827193", "names": ["Uveal Melanoma by Gene Expression Profile"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uveal Melanoma by Gene Expression Profile", "shortest_name_length": 41}
{"curie": "UMLS:C0343404", "names": ["morganella infection", "Morganella infection", "Proteus morganii infection", "morganella morganii infection", "Morganella morganii infection", "Morganella infection (disorder)", "infection due to Proteus morganii", "Bacterial infection due to Proteus morganii", "infection due to Proteus morganii (diagnosis)", "Bacterial infection due to Morganella morganii", "Bacterial infection caused by Proteus morganii", "Bacterial infection caused by Morganella morganii", "Bacterial infection caused by Morganella morganii (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Morganella infection", "shortest_name_length": 20}
{"curie": "MONDO:0001731", "names": ["benign vaginal carcinosarcoma", "benign vaginal mixed epithelial and mesenchymal tumor", "Benign Vaginal Mixed Epithelial and Mesenchymal Tumor", "benign vaginal mixed epithelial and mesenchymal neoplasm", "Benign Vaginal Mixed Epithelial and Mesenchymal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign vaginal mixed epithelial and mesenchymal neoplasm", "shortest_name_length": 29}
{"curie": "UMLS:C1696113", "names": ["Uterine Obstruction", "uterine obstruction", "Uterine obstruction", "uterine obstruction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Obstruction", "shortest_name_length": 19}
{"curie": "UMLS:C4683612", "names": ["Lugano Classification Advanced Stage Adult Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Advanced Stage Adult Hodgkin Lymphoma AJCC v8", "shortest_name_length": 67}
{"curie": "MONDO:0000144", "names": ["pregnancy loss, recurrent, susceptibility"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pregnancy loss, recurrent, susceptibility", "shortest_name_length": 41}
{"curie": "MONDO:0013767", "names": ["RALD", "ALPS4", "ALPS type 4", "ALPS type IV", "NRAS autoimmune lymphoproliferative syndrome", "autoimmune lymphoproliferative syndrome type 4", "Autoimmune lymphoproliferative syndrome type 4", "autoimmune lymphoproliferative syndrome, type 4", "autoimmune lymphoproliferative syndrome type IV", "Autoimmune lymphoproliferative syndrome type IV", "AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IV", "RAS-associated autoimmune leukoproliferative disease", "RAS-associated autoimmune leucoproliferative disease", "RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER", "RAS-associated autoimmune leukoproliferative disorder", "RALD - RAS-associated autoimmune leukoproliferative disease", "RALD - RAS-associated autoimmune leucoproliferative disease", "RAS-associated autoimmune leukoproliferative disease (disorder)", "autoimmune lymphoproliferative syndrome caused by mutation in NRAS", "RAS-associated autoimmune lymphoproliferative syndrome type IV, somatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune lymphoproliferative syndrome type 4", "shortest_name_length": 4}
{"curie": "MONDO:0010031", "names": ["SLS", "FAO deficiency", "FADH deficiency", "Sjögren-Larsson", "FALDH deficiency", "FALDH Deficiency", "FALDH DEFICIENCY", "ichthyotic idiocy", "Sjögren-Larsson Syndrome", "Sjogren Larsson Syndrome", "Sjögren-Larsson syndrome", "Sjogren Larsson syndrome", "Sjogren-Larsson Syndrome", "Sjogren-Larsson syndrome", "SJOGREN-LARSSON SYNDROME", "Sjoegren-Larsson syndrome", "Sjogren-Larsson's syndrome", "Sjogren-Larsson syndrome (SLS)", "Ichthyosis Oligophrenia Syndrome", "oligophrenia-ichthyosis syndrome", "Sjögren-Larsson syndrome (disorder)", "fatty aldehyde dehydrogenase deficiency", "Fatty Aldehyde Dehydrogenase Deficiency", "FATTY ALDEHYDE DEHYDROGENASE DEFICIENCY", "Fatty Alcohol:NAD+ Oxidoreductase Deficiency", "Fatty acid alcohol oxidoreductase deficiency", "fatty acid alcohol oxidoreductase deficiency", "FATTY ALCOHOL:NAD+ OXIDOREDUCTASE DEFICIENCY", "fatty alcohol:NAD+ oxidoreductase deficiency", "Fatty Aldehyde Dehydrogenase Deficiency Disease", "ICHTHYOSIS, SPASTIC NEUROLOGIC DISORDER, AND OLIGOPHRENIA", "Ichthyosis, Spastic Neurologic Disorder, and Oligophrenia", "ichthyosis, spastic neurologic disorder, and oligophrenia", "mental deficiency-spasticity-congenital ichthyosis syndrome", "Congenital Icthyosis Mental Retardation Spasticity Syndrome", "ichthyosis-spastic neurologic disorder-oligophrenia syndrome", "congenital ichthyosis-mental retardation-spasticity syndrome", "Fatty alcohol-nicotinamide adenine dinucleotide oxidoreductase deficiency", "spastic quadriplegia-congenital ichthyosiform erythroderma-oligophrenia syndrome", "FAO - Fatty alcohol-nicotinamide adenine dinucleotide oxidase-reductase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sjogren-Larsson syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0003078", "names": ["metastatic retinoblastoma", "Metastatic Retinoblastoma", "extraocular retinoblastoma", "Extraocular Retinoblastoma", "Extraocular retinoblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extraocular retinoblastoma", "shortest_name_length": 25}
{"curie": "MONDO:0010452", "names": ["MRX90", "XLID90", "X-linked mental retardation 90", "MENTAL RETARDATION, X-LINKED 90", "mental retardation, X-linked 90", "mental retardation, X-linked type 90", "intellectual disability, X-linked 90", "intellectual disability, X-linked type 90", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 90", "non-syndromic X-linked intellectual disability 90", "DLG3 non-syndromic X-linked intellectual disability", "intellectual developmental disorder, X-linked 90, X-linked recessive", "non-syndromic X-linked intellectual disability caused by mutation in DLG3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 90", "shortest_name_length": 5}
{"curie": "UMLS:C5447383", "names": ["Repeat expansion", "Repeat Expansion Disease", "Expansion Repeat Disease", "Repeat Expansion Disorder", "Expansion Repeat Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Repeat Expansion Disease", "shortest_name_length": 16}
{"curie": "MONDO:0010239", "names": ["SBH", "LISX", "SCLH", "Xlis", "XLIS", "XLIS1", "LISX1", "Dc syndrome", "X-linked lissencephaly", "X-Linked Lissencephaly", "Double cortex syndrome", "X Linked Lissencephaly", "lissencephaly X-linked", "Lissencephaly, X Linked", "Lissencephaly, X-Linked", "lissencephaly, X-linked", "X-Linked Lissencephalies", "X-linked lissencephaly 1", "Lissencephalies, X-Linked", "lissencephaly, X-linked, 1", "Lissencephaly, X-Linked, 1", "LISSENCEPHALY, X-LINKED, 1", "X-linked lissencephaly type 1", "lissencephaly, X-linked, type 1", "Subcortical Band Heterotopia, X-Linked", "SUBCORTICAL BAND HETEROTOPIA, X-LINKED", "subcortical band heterotopia, X-linked", "Subcortical laminar heterotopia, X-linked", "SUBCORTICAL LAMINAR HETEROTOPIA, X-LINKED", "subcortical laminal heterotopia, X-linked", "subcortical laminar heterotopia, X-linked", "subcortical laminar heterotopia, X-linked,", "lissencephaly and agenesis of corpus callosum", "Lissencephaly and agenesis of corpus callosum", "LISSENCEPHALY AND AGENESIS OF CORPUS CALLOSUM", "Lissencephaly type 1 due to doublecortin gene mutation", "lissencephaly type 1 due to doublecortin gene mutation", "Lissencephaly type 1 due to doublecortin gene mutation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lissencephaly type 1 due to doublecortin gene mutation", "shortest_name_length": 3}
{"curie": "MONDO:0049223", "names": ["OI19", "osteogenesis imperfecta type 19", "osteogenesis imperfecta, type 19", "osteogenesis imperfecta type XIX", "Osteogenesis Imperfecta Type XIX", "OSTEOGENESIS IMPERFECTA, TYPE XIX", "osteogenesis imperfecta, type XIX", "osteogenesis imperfecta, type XIX, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteogenesis imperfecta, type 19", "shortest_name_length": 4}
{"curie": "UMLS:C0685896", "names": ["acephali", "Acephaly", "acephaly", "Acephalia", "Acephalus", "acephalus", "Acephaly (disorder)", "Congenital absence of head"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acephaly", "shortest_name_length": 8}
{"curie": "MONDO:0014010", "names": ["ARCI9", "autosomal recessive congenital ichthyosis 9", "ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 9", "ichthyosis, congenital, autosomal recessive 9", "autosomal recessive congenital ichthyosis type 9", "ichthyosis, congenital, autosomal recessive type 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive congenital ichthyosis 9", "shortest_name_length": 5}
{"curie": "MONDO:0006135", "names": ["Cervix Clear Cell Carcinoma", "cervix clear cell carcinoma", "Cervical Clear Cell Carcinoma", "cervical clear cell carcinoma", "clear cell carcinoma of cervix", "Clear cell carcinoma of cervix", "Clear Cell Carcinoma of Cervix", "Cervix Clear Cell Adenocarcinoma", "cervix clear cell adenocarcinoma", "cervix uteri clear cell carcinoma", "Cervix Uteri Clear Cell Carcinoma", "Clear Cell Carcinoma of the Cervix", "clear cell carcinoma of the cervix", "Cervical Clear Cell Adenocarcinoma", "Cervical clear cell adenocarcinoma", "cervical clear cell adenocarcinoma", "clear cell adenocarcinoma of cervix", "Clear Cell Adenocarcinoma of Cervix", "Uterine Cervix Clear Cell Carcinoma", "uterine cervix clear cell carcinoma", "clear cell carcinoma of cervix uteri", "Clear Cell Carcinoma of Cervix Uteri", "Clear Cell Carcinoma of Uterine Cervix", "Cervix Uteri Clear Cell Adenocarcinoma", "cervix uteri clear cell adenocarcinoma", "clear cell carcinoma of uterine cervix", "Clear Cell Adenocarcinoma of the Cervix", "clear cell adenocarcinoma of the cervix", "Clear cell carcinoma of the Cervix Uteri", "uterine cervix clear cell adenocarcinoma", "Uterine Cervix Clear Cell Adenocarcinoma", "clear cell carcinoma of the cervix uteri", "Clear Cell Carcinoma of the Cervix Uteri", "clear cell adenocarcinoma of cervix uteri", "Clear Cell Adenocarcinoma of Cervix Uteri", "clear cell carcinoma of the uterine cervix", "Clear Cell Carcinoma of the Uterine Cervix", "clear cell adenocarcinoma of uterine cervix", "Clear Cell Adenocarcinoma of Uterine Cervix", "Clear Cell Adenocarcinoma of the Cervix Uteri", "clear cell adenocarcinoma of the cervix uteri", "clear cell adenocarcinoma of cervix (diagnosis)", "Clear Cell Adenocarcinoma of the Uterine Cervix", "clear cell adenocarcinoma of the uterine cervix", "HPV- Independent Cervical Adenocarcinoma, Clear Cell-Type", "HPV- Independent Cervical Adenocarcinoma, Clear Cell Type", "Human Papillomavirus-Independent Cervical Adenocarcinoma, Clear Cell Type", "Human Papillomavirus-Independent Cervical Adenocarcinoma, Clear Cell-Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical clear cell adenocarcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0017131", "names": ["genetic cardiac anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genetic cardiac anomaly", "shortest_name_length": 23}
{"curie": "MONDO:0004218", "names": ["Brain Germ Cell Tumor", "Brain germ cell tumor", "Pediatric Brain Germ Cell Tumor", "childhood brain germ cell tumor", "pediatric brain germ cell tumor", "childhood germ cell brain tumor", "Childhood Germ Cell Brain Tumor", "Childhood Brain Germ Cell Tumor", "childhood germ cell brain tumour", "childhood brain tumor, germ cell", "germ cell brain tumor, childhood", "brain tumor, pediatric, germ cell", "brain tumor, germ cell, childhood", "brain tumor, childhood, germ cell", "pediatric brain germ cell neoplasm", "Germ Cell Tumor of Childhood Brain", "childhood germ cell brain neoplasm", "Germ Cell Tumor of Pediatric Brain", "Pediatric Brain Germ Cell Neoplasm", "Childhood Germ Cell Brain Neoplasm", "germ cell tumor of pediatric brain", "germ cell tumor of childhood brain", "childhood brain germ cell neoplasm", "Childhood Brain Germ Cell Neoplasm", "Germ Cell Neoplasm of Pediatric Brain", "Germ Cell Neoplasm of Childhood Brain", "germ cell neoplasm of pediatric brain", "germ cell neoplasm of childhood brain", "Germ Cell Tumor of the Pediatric Brain", "childhood intracranial germ cell tumor", "Germ Cell Tumor of the Childhood Brain", "germ cell tumor of the childhood brain", "germ cell tumor of the pediatric brain", "germ cell neoplasm of the childhood brain", "Germ Cell Neoplasm of the Pediatric Brain", "Germ Cell Neoplasm of the Childhood Brain", "germ cell neoplasm of the pediatric brain", "childhood malignant germ cell brain tumor", "germ cell neoplasm of the paediatric brain", "childhood intracranial germ cell CNS tumor", "intracranial germ cell CNS tumor, childhood", "CNS tumor, pediatric intracranial germ cell", "childhood CNS tumor, intracranial germ cell", "CNS tumor, childhood intracranial germ cell", "intracranial germ cell brain tumor, childhood", "childhood brain tumor, intracranial germ cell", "brain tumor, intracranial germ cell, childhood", "brain tumor, childhood, intracranial germ cell", "brain tumor, pediatric, intracranial germ cell", "childhood malignant intracranial germ cell brain tumor", "central nervous system tumor, intracranial germ cell, childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood germ cell brain tumor", "shortest_name_length": 21}
{"curie": "MONDO:0001810", "names": ["disorder of XII nerve", "Disorder of XII Nerve", "disorder of 12th nerve", "Twelfth Nerve Disorder", "twelfth nerve disorder", "n.hypoglossus; disorder", "Disorders of 12th nerve", "Hypoglossal nerve lesion", "hypoglossal nerve disease", "disorder of the XII nerve", "Disorder of the XII Nerve", "Hypoglossal Nerve Disease", "Hypoglossal Nerve Diseases", "disorder hypoglossal nerve", "Hypoglossal nerve disorder", "Hypoglossal Nerve Disorder", "hypoglossal nerve disorder", "Cranial Nerve XII Diseases", "Hypoglossal nerve disorders", "Cranial Nerve XII Disorders", "Disorder of cranial nerve 12", "disease of hypoglossal nerve", "Disorder of hypoglossal nerve", "disorder of hypoglossal nerve", "Hypoglossal nerve disorder NOS", "Twelfth Cranial Nerve Diseases", "Twelfth cranial nerve disorder", "Twelfth Cranial Nerve Disorder", "Disorders of hypoglossal nerve", "Disorders of 12th cranial nerve", "Disorder of hypoglossal nerve, NOS", "Disorders of the XIIth cranial nerve", "disorder of hypoglossal [12th] nerve", "Disorder of the twelfth cranial nerve", "hypoglossal nerve disease or disorder", "Hypoglossal nerve disease or syndrome", "Disorders of hypoglossal [12th] nerve", "Disorders of the twelfth cranial nerve", "Disorder of hypoglossal nerve (disorder)", "disease or disorder of hypoglossal nerve", "disease (or disorder); nerve, hypoglossal", "Twelfth cranial nerve disease or syndrome", "disorder of hypoglossal nerve (diagnosis)", "Disorder of the twelfth cranial nerve, NOS", "cranial nerve; disorder, twelfth (hypoglossal)", "disease (or disorder); cranial nerve, twelfth (hypoglossal)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypoglossal nerve disorder", "shortest_name_length": 21}
{"curie": "MONDO:0007225", "names": ["Fibular aplasia ectrodactyly", "fibular aplasia ectrodactyly", "fibular aplasia-ectrodactyly syndrome", "brachydactyly-ectrodactyly with fibular aplasia or hypoplasia", "Brachydactyly-ectrodactyly with fibular aplasia or hypoplasia", "BRACHYDACTYLY-ECTRODACTYLY WITH FIBULAR APLASIA OR HYPOPLASIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibular aplasia-ectrodactyly syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0060562", "names": ["NELABA", "LIPT2D", "LIPOYLTRANSFERASE 2 DEFICIENCY", "lipoyltransferase 2 deficiency", "encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities", "ENCEPHALOPATHY, NEONATAL SEVERE, WITH LACTIC ACIDOSIS AND BRAIN ABNORMALITIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities", "shortest_name_length": 6}
{"curie": "UMLS:C5204070", "names": ["Metastatic Prostate Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Prostate Neuroendocrine Carcinoma", "shortest_name_length": 44}
{"curie": "MONDO:0020937", "names": ["contractures, pterygia, and variable skeletal fusions syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "contractures, pterygia, and variable skeletal fusions syndrome", "shortest_name_length": 62}
{"curie": "MONDO:0035460", "names": ["idiopathic steroid-resistant nephrotic syndrome with sensitivity to intensified immunosuppression", "idiopathic steroid-resistant nephrotic syndrome with sensitivity to second-line immunosuppressive therapy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic steroid-resistant nephrotic syndrome with sensitivity to second-line immunosuppressive therapy", "shortest_name_length": 97}
{"curie": "MONDO:0005313", "names": ["NEC", "necrotising enterocolitis", "ENTEROCOLITIS NECROTIZING", "Enterocolitis necrotizing", "Necrotising enterocolitis", "Enterocolitis necrotising", "Necrotizing enterocolitis", "Necrotizing Enterocolitis", "ENTEROCOLITIS NECROTISING", "necrotizing enterocolitis", "enterocolitis necrotizing", "ENTEROCOLITIS, NECROTIZING", "Enterocolitis, Necrotizing", "enterocolitis nec necrotizing", "Necrotizing enterocolitis, NOS", "NEC - Necrotising enterocolitis", "NEC - Necrotizing enterocolitis", "enterocolitis necrotizing neonatal", "Perinatal necrotizing enterocolitis", "perinatal necrotizing enterocolitis", "Perinatal necrotising enterocolitis", "necrotizing enterocolitis (diagnosis)", "Pseudomembranous enterocolitis in newborn", "enteritis; necrotizing of fetus or newborn", "necrotizing of fetus or newborn; enteritis", "Necrotizing Enterocolitis in Fetus or Newborn", "Necrotizing enterocolitis in fetus OR newborn", "Necrotizing enterocolitis in fetus or newborn", "necrotizing enterocolitis in fetus or newborn", "Necrotising enterocolitis in fetus OR newborn", "Necrotizing enterocolitis of fetus and newborn", "Perinatal necrotizing enterocolitis (disorder)", "Necrotizing enterocolitis in foetus or newborn", "Necrotising enterocolitis of fetus and newborn", "Necrotising enterocolitis in foetus OR newborn", "perinatal necrotizing enterocolitis (diagnosis)", "perinatal necrotizing enterocolitis in fetus or newborn", "Necrotizing enterocolitis in fetus OR newborn (disorder)", "necrotizing enterocolitis in fetus or newborn (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "necrotizing enterocolitis", "shortest_name_length": 3}
{"curie": "MONDO:0002449", "names": ["nodular corneal degeneration", "Nodular corneal degeneration", "Nodular degeneration of cornea", "nodular degeneration of cornea", "nodular corneal degeneration (diagnosis)", "Nodular degeneration of cornea (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nodular degeneration of cornea", "shortest_name_length": 28}
{"curie": "MONDO:0015045", "names": ["IPSID", "ipsid", "Alpha-HCD", "ALPHA HCD", "heavy chain alpha", "ALPHA CHAIN DISEASE", "alpha-chain disease", "alpha-Chain Disease", "chain alpha disease", "alpha Chain Disease", "Seligmann's disease", "alpha chain disease", "alpha-Chain disease", "Disease, alpha-Chain", "alpha-Chain Diseases", "Diseases, alpha-Chain", "Mediterranean lymphoma", "Mediterranean Lymphoma", "IGA HEAVY CHAIN DISEASE", "Mediterraneanl lymphoma", "lymphoma; mediterranean", "Lymphoma, Mediterranean", "mediterranean; lymphoma", "IgA heavy chain disease", "Alpha Heavy Chain Disease", "ALPHA HEAVY CHAIN DISEASE", "alpha-heavy chain disease", "ALPHA-HEAVY CHAIN DISEASE", "heavy chain disease alpha", "Alpha heavy chain disease", "Alpha-heavy chain disease", "alpha heavy chain; disease", "disease; alpha heavy chain", "IgA heavy chain disease, NOS", "Heavy chain disease, IgA type", "Heavy Chain Disease, IgA Type", "IgA heavy chain paraproteinemia", "Mediterranean abdominal lymphoma", "alpha; alpha heavy chain disease", "Immunoproliferative disease, NOS", "Mediterranean Abdominal Lymphoma", "Mediterranean lymphoma (clinical)", "Alpha heavy chain disease (disorder)", "Alpha heavy chain disease (clinical)", "Alpha heavy chain disease (diagnosis)", "heavy chain disease alpha, enteric form", "Alpha heavy chain disease, enteric form", "disease (or disorder); alpha heavy chain", "disease (or disorder); heavy chain, alpha", "IMMUNOPROLIFERATIVE SMALL INTESTINE DISEASE", "immunoproliferative small intestinal disease", "Immunoproliferative small intestinal disease", "Immunoproliferative Small Intestinal Disease", "immunoproliferative; disease, small intestine", "Alpha heavy chain disease, enteric form (disorder)", "Alpha heavy chain disease, enteric form (diagnosis)", "Immunoproliferative small intestinal disease (clinical)", "Immunoproliferative small intestinal disease (disorder)", "immunoproliferative small intestinal disease (diagnosis)", "disease (or disorder); immunoproliferative, small intestine", "Immunoproliferative small intestinal disease (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alpha-heavy chain disease", "shortest_name_length": 5}
{"curie": "MONDO:0002680", "names": ["CWD", "Chronic Wasting Disease", "chronic wasting disease", "Chronic wasting disease", "Wasting Disease, Chronic", "Chronic wasting disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic wasting disease", "shortest_name_length": 3}
{"curie": "MONDO:0004107", "names": ["splenic leukemia", "spleen leukemia (disease)", "leukemia (disease) of spleen", "splenic manifestation of leukemia", "Splenic Manifestation of Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "splenic manifestation of leukemia", "shortest_name_length": 16}
{"curie": "UMLS:C4524799", "names": ["Gastric Cancer by AJCC v8 ypTNM Stage", "Gastric Cancer by AJCC v8 Postneoadjuvant Therapy Stage", "Gastric Carcinoma by AJCC v8 Postneoadjuvant Therapy Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Cancer by AJCC v8 Postneoadjuvant Therapy Stage", "shortest_name_length": 37}
{"curie": "MONDO:0006853", "names": ["CHONDROSARCOMA MESENCHYMAL", "Mesenchymal chondrosarcoma", "Mesenchymal Chondrosarcoma", "mesenchymal chondrosarcoma", "chondrosarcoma mesenchymal", "Chondrosarcoma, Mesenchymal", "Mesenchymal Chondrosarcomas", "Chondrosarcomas, Mesenchymal", "Mesenchymal chondrosarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mesenchymal chondrosarcoma", "shortest_name_length": 26}
{"curie": "MONDO:0015004", "names": ["DYT28", "Dystonia 28", "KMT2B-related dystonia", "KMT2B dystonic disorder", "DYSTONIA 28, CHILDHOOD-ONSET", "dystonia 28, childhood-onset", "dystonia 28, childhood-onset; DYT28", "dystonic disorder caused by mutation in KMT2B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dystonia 28, childhood-onset", "shortest_name_length": 5}
{"curie": "UMLS:C2931716", "names": ["Deafness, autosomal dominant nonsyndromic sensorineural 17", "Late-onset progressive hereditary hearing impairment due to cochleosaccular degeneration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Deafness, autosomal dominant nonsyndromic sensorineural 17", "shortest_name_length": 58}
{"curie": "MONDO:0013598", "names": ["MSLHP", "muscle hypertrophy", "Muscle Hypertrophy Syndrome", "Muscle hypertrophy syndrome", "myostatin-related muscle hypertrophy", "Myostatin-related muscle hypertrophy", "Myostatin related hypertrophy of muscle", "Myostatin related hypertrophy of muscle (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myostatin-related muscle hypertrophy", "shortest_name_length": 5}
{"curie": "MONDO:0018661", "names": ["Zika", "Zika NOS", "Zika fever", "Zika Fever", "zika virus", "Fever, Zika", "fever; Zika", "fever, Zika", "Zika; fever", "ZikV Infection", "ZikV infection", "Infection, ZikV", "Zika Virus Disease", "Zika virus disease", "Disease, Zika Virus", "Virus Disease, Zika", "Zika virus infection", "Zika Virus Infection", "Infection, Zika Virus", "Virus Infection, Zika", "zika virus (diagnosis)", "congenital Zika syndrome", "Zika virus disease (disorder)", "Zika virus infectious disease", "Zika virus disease or disorder", "congenital Zika virus infection", "Mosquito-borne viral fever, Zika", "Zika virus caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Zika virus infectious disease", "shortest_name_length": 4}
{"curie": "MONDO:0017969", "names": ["46,XY DSD of endocrine origin", "46,XY disorder of sex development of endocrine origin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XY disorder of sex development of endocrine origin", "shortest_name_length": 29}
{"curie": "MONDO:0021521", "names": ["Benign Mediastinal Tumor", "benign mediastinal tumor", "mediastinum benign neoplasm", "benign tumor of mediastinum", "Benign mediastinal neoplasm", "Benign Mediastinal Neoplasm", "Benign Tumor of Mediastinum", "Benign tumor of mediastinum", "benign mediastinal neoplasm", "Mediastinal neoplasms benign", "Benign tumour of mediastinum", "benign neoplasm of mediastinum", "Benign Neoplasm of Mediastinum", "Benign neoplasm of mediastinum", "Benign mediastinal neoplasm NOS", "benign tumor of the mediastinum", "Benign Tumor of the Mediastinum", "Benign Mediastinal Neoplasms NOS", "benign neoplasm of the mediastinum", "Benign Neoplasm of the Mediastinum", "Benign neoplasm of mediastinum, NOS", "Benign neoplasm of mediastinum (disorder)", "benign neoplasm of mediastinum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of mediastinum", "shortest_name_length": 24}
{"curie": "UMLS:C5420815", "names": ["Uveal Nevus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uveal Nevus", "shortest_name_length": 11}
{"curie": "MONDO:0001266", "names": ["Ergotism", "ergotism", "ERGOTISM", "Ergotisms", "Erysipelas", "ERYSIPELAS", "erysipelas", "Ergotism, NOS", "ergot poisoning", "Ergot Poisoning", "Ergot poisoning", "Ergot Poisonings", "St. Anthony Fire", "anthonys fire st", "Poisoning, Ergot", "St Anthony's fire", "Poisonings, Ergot", "st. anthonys fire", "anthony's fire st", "St. Anthonys Fire", "Fire, St. Anthonys", "St. Anthony's Fire", "SAINT ANTHONY FIRE", "st. anthony's fire", "Saint Anthony Fire", "anthony fire saint", "fire; St Anthony's", "Saint Anthonys Fire", "Patch of erysipelas", "Ergotism (disorder)", "Saint Anthony's Fire", "saint anthony's fire", "Erysipelas (disorder)", "infection; erysipelas", "erysipelas; infection", "erysipelas (diagnosis)", "Ergot causing toxic effect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erysipelas", "shortest_name_length": 8}
{"curie": "MONDO:0020143", "names": ["Cerebral lipidoses", "Cerebral lipidosis", "cerebral lipidosis", "cerebral; lipidosis", "lipidosis; cerebral", "Cerebral lipidosis, NOS", "Cerebral lipidosis (disorder)", "cerebral lipidosis with dementia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral lipidosis with dementia", "shortest_name_length": 18}
{"curie": "UMLS:C5555132", "names": ["Metastatic Low Grade Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Low Grade Astrocytoma", "shortest_name_length": 32}
{"curie": "MONDO:0033013", "names": ["EKVP3", "erythrokeratodermia variabilis et progressiva 3", "erythrokeratodermia variabilis ET progressiva 3", "ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythrokeratodermia variabilis et progressiva 3", "shortest_name_length": 5}
{"curie": "MONDO:0018161", "names": ["non-hereditary retinoblastoma", "retinoblastoma (nonhereditary)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-hereditary retinoblastoma", "shortest_name_length": 29}
{"curie": "MONDO:0000485", "names": ["Dysphonia", "spastic dysphonia", "laryngeal dystonia", "Laryngeal dystonia", "spasmodic dystonia", "spasmodic dysphonia", "Spasmodic dysphonia", "laryngeal dyskinesia", "adductor spasmodic dysphonia", "abductor spasmodic dysphonia", "Laryngeal dystonia (disorder)", "mixed spasmodic dysphonia (type)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spasmodic dystonia", "shortest_name_length": 9}
{"curie": "MONDO:0001847", "names": ["Nuclear senile cataract", "nuclear senile cataract", "Senile nuclear cataract", "Senile nuclear sclerosis", "nuclear; senile cataract", "senile cataract; nuclear", "lens nucleus senile cataract", "senile cataract of lens nucleus", "Nuclear senile cataract (disorder)", "nuclear senile cataract (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nuclear senile cataract", "shortest_name_length": 23}
{"curie": "MONDO:0014353", "names": ["IVMS", "IMD23", "IMD 23", "PGM3-CDG", "PGM3 deficiency", "PGM3 Deficiency", "Immunodeficiency 23", "immunodeficiency 23", "IMMUNODEFICIENCY 23", "immunodeficiency type 23", "CID due to PGM3 deficiency", "phosphoglucomutase 3 deficiency", "PGM3-Associated Immunodeficiency", "PGM3 Phosphoglucomutase Deficiency", "phosphoglucomutase deficiency type 3", "Combined Inflammatory and Immunologic Defect", "combined inflammatory and immunologic defect", "immunodeficiency-vasculitis-myoclonus syndrome", "IMMUNODEFICIENCY-VASCULITIS-MYOCLONUS SYNDROME", "PGM3-EXACT congenital disorder of glycosylation", "combined immunodeficiency due to PGM3 deficiency", "Combined immunodeficiency due to PGM3 deficiency", "PGM3-related congenital disorder of glycosylation", "IMMUNODEFICIENCY WITH HYPER IgE AND COGNITIVE IMPAIRMENT", "immunodeficiency with hyper IgE and cognitive impairment", "Phosphoglucomutase 3-related congenital disorder of glycosylation", "Combined immunodeficiency due to PGM3 (phosphoglucomutase 3) deficiency", "PGM3-CDG - phosphoglucomutase 3-related congenital disorder of glycosylation", "Phosphoglucomutase 3-related congenital disorder of glycosylation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 23", "shortest_name_length": 4}
{"curie": "MONDO:0010162", "names": ["TYRSN3", "Tyrosinemia type 3", "tyrosinemia type 3", "Tyrosinaemia type 3", "tyrosinemia, type 3", "Type III Tyrosinemia", "Tyrosinemia type III", "tyrosinemia type III", "Tyrosinaemia type III", "Tyrosinemia, Type III", "Type III Tyrosinemias", "TYROSINEMIA, TYPE III", "Tyrosinemia, type III", "tyrosinemia, type III", "Tyrosinemias, Type III", "Tyrosinemia type III (disorder)", "tyrosinemia type III (diagnosis)", "Hereditary Tyrosinemia, Type III", "tyrosinemia due to HPD deficiency", "Tyrosinemia due to HPD deficiency", "4-Hydroxyphenylpyruvic acid oxidase deficiency", "4-HYDROXYPHENYLPYRUVATE DIOXYGENASE DEFICIENCY", "4-Hydroxyphenylpyruvate dioxygenase deficiency", "4-Hydroxyphenylpyruvate hydroxylase deficiency", "4-HYDROXYPHENYLPYRUVIC ACID OXIDASE DEFICIENCY", "4-Hydroxyphenylpyruvate Dioxygenase Deficiency", "4-Hydroxyphenylpyruvic Acid Oxidase Deficiency", "Dioxygenase Deficiency, 4-Hydroxyphenylpyruvate", "Deficiency, 4-Hydroxyphenylpyruvate Dioxygenase", "Deficiencies, 4-Hydroxyphenylpyruvate Dioxygenase", "Dioxygenase Deficiencies, 4-Hydroxyphenylpyruvate", "4-alpha hydroxyphenylpyruvate dioxygenase deficiency", "4-alpha hydroxyphenylpyruvic acid oxidase deficiency", "4 Hydroxyphenylpyruvate Dioxygenase Deficiency Disease", "4-Hydroxyphenol Pyruvic Acid Oxidase Deficiency Disease", "4 Hydroxyphenol Pyruvic Acid Oxidase Deficiency Disease", "Deficiency Disease, 4-Hydroxyphenol Pyruvic Acid Oxidase", "Deficiency Disease, 4 Hydroxyphenol Pyruvic Acid Oxidase", "4-Hydroxyphenylpyruvate dioxygenase deficiency (disorder)", "Tyrosinemia due to 4-hydroxyphenylpyruvic acid oxidase deficiency", "Tyrosinemia due to 4-hydroxyphenylpyruvate dioxygenase deficiency", "tyrosinemia due to 4-hydroxyphenylpyruvate dioxygenase deficiency", "tyrosinemia due to 4-hydroxyphenylpyruvic acid oxidase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tyrosinemia type III", "shortest_name_length": 6}
{"curie": "UMLS:C5667241", "names": ["Advanced Pleomorphic Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Pleomorphic Liposarcoma", "shortest_name_length": 32}
{"curie": "UMLS:C5555189", "names": ["Refractory Primary Peritoneal Low Grade Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Primary Peritoneal Low Grade Serous Adenocarcinoma", "shortest_name_length": 61}
{"curie": "MONDO:0006806", "names": ["IU", "Pars Planitis", "pars planitis", "iritis chronic", "chronic iritis", "Chronic Cyclitis", "Chronic cyclitis", "chronic cyclitis", "Cyclitis, Chronic", "Peripheral uveitis", "uveitis intermediate", "intermediate uveitis", "Intermediate uveitis", "Intermediate Uveitis", "Uveitis, Intermediate", "peripheral uveoretinitis", "Peripheral uveoretinitis", "intermediate uveitis (disease)", "Intermediate uveitis (disorder)", "Intermediate uveitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intermediate uveitis", "shortest_name_length": 2}
{"curie": "UMLS:C0948979", "names": ["Catheter site discharge"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Catheter site discharge", "shortest_name_length": 23}
{"curie": "UMLS:C1504525", "names": ["Acute lymphoblastic leukemia recurrent", "Recurrent Acute Lymphoblastic Leukemia", "Acute lymphoblastic leukaemia recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute lymphoblastic leukemia recurrent", "shortest_name_length": 38}
{"curie": "MONDO:0006274", "names": ["VIN 1", "Grade I VIN", "Grade 1 VIN", "grade I VIN", "VIN grade 1", "Vulvar LSIL", "grade 1 VIN", "VIN Grade 1", "Low Grade VIN", "low grade VIN", "VIN 1 of usual type", "VIN 1 of Usual Type", "dysplasia mild vulva", "vulvar flat condyloma", "Vulvar Flat Condyloma", "Mild vulvar dysplasia", "vulvar mild dysplasia", "dysplasia; vulva, mild", "Mild dysplasia of vulva", "mild dysplasia of vulva", "vulvar mild squamous dysplasia", "Vulvar Mild Squamous Dysplasia", "mild dysplasia of vulva (diagnosis)", "vulva intraepithelial neoplasia grade 1", "Vulva Intraepithelial Neoplasia Grade 1", "grade I vulvar intraepithelial neoplasia", "vulvar intraepithelial neoplasia grade 1", "Vulvar Intraepithelial Neoplasia Grade 1", "Vulval intraepithelial neoplasia grade I", "vulval intraepithelial neoplasia grade 1", "Grade 1 Vulvar Intraepithelial Neoplasia", "vulvar intraepithelial neoplasia grade I", "Vulval intraepithelial neoplasia grade 1", "grade 1 vulvar intraepithelial neoplasia", "Grade I Vulvar Intraepithelial Neoplasia", "vulva; intraepithelial neoplasia, grade I", "intraepithelial neoplasia of vulva grade 1", "Low Grade Vulvar Intraepithelial Neoplasia", "Intraepithelial Neoplasia of Vulva Grade 1", "low grade vulvar intraepithelial neoplasia", "neoplasia; intraepithelial, vulva, grade I", "Vulvar intraepithelial neoplasia I [VIN I]", "intraepithelial neoplasia of the vulva grade 1", "Intraepithelial Neoplasia of the Vulva Grade 1", "VIN - Vulval intraepithelial neoplasia grade 1", "Vulvar intraepithelial neoplasia [VIN], grade I", "Vulvar Intraepithelial Neoplasia 1 of Usual Type", "vulvar Low grade squamous intraepithelial lesion", "vulvar intraepithelial neoplasia 1 of usual type", "Vulvar Low-Grade Squamous Intraepithelial Lesion", "Vulvar Low Grade Squamous Intraepithelial Lesion", "vulvar Low-grade squamous intraepithelial lesion", "Low Grade Vulvar Squamous Intraepithelial Lesion", "Vulval intraepithelial neoplasia grade 1 (disorder)", "vulvar squamous cell intraepithelial neoplasia, grade I", "squamous cell intraepithelial neoplasia of vulva, grade I", "squamous cell intraepithelial neoplasia of vulva, grade I (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "low grade vulvar intraepithelial neoplasia", "shortest_name_length": 5}
{"curie": "MONDO:0020499", "names": ["Nipah fever", "Nipah encephalitis", "Nipah virus disease", "Nipah virus encephalitis", "Nipah virus infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nipah virus disease", "shortest_name_length": 11}
{"curie": "MONDO:0019268", "names": ["epidermal disease", "rare epidermal disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermal disease", "shortest_name_length": 17}
{"curie": "MONDO:0032874", "names": ["CILD43", "primary ciliary dyskinesia 43", "CILIARY DYSKINESIA, PRIMARY, 43", "ciliary dyskinesia, primary, 43", "primary ciliary dyskinesia 43 with or without situs inversus", "Ciliary Dyskinesia, Primary, 43, With or Without Situs Inversus", "CILIARY DYSKINESIA, PRIMARY, 43, WITH OR WITHOUT SITUS INVERSUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ciliary dyskinesia, primary, 43", "shortest_name_length": 6}
{"curie": "UMLS:C4524798", "names": ["Tumor Stage (Pathologic)", "Gastric Cancer by AJCC v8 pTNM Stage", "Gastric Cancer by AJCC v8 Pathologic Stage", "Gastric Carcinoma by AJCC v8 Pathologic Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Cancer by AJCC v8 Pathologic Stage", "shortest_name_length": 24}
{"curie": "UMLS:C2984083", "names": ["Fallopian Tube Cancer by AJCC v7 Stage", "Fallopian Tube Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fallopian Tube Cancer by AJCC v7 Stage", "shortest_name_length": 38}
{"curie": "UMLS:C2747816", "names": ["Severe Malaria", "Severe malaria", "Complicated Malaria", "Complicated malaria", "Complicated malaria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Complicated malaria", "shortest_name_length": 14}
{"curie": "MONDO:0017892", "names": ["SYNE1-related AMC", "autosomal recessive myogenic AMC", "Autosomal recessive myogenic AMC", "SYNE1-related arthrogryposis multiplex congenita", "Autosomal recessive myogenic arthrogryposis multiplex congenita", "autosomal recessive myogenic arthrogryposis multiplex congenita", "Autosomal recessive myogenic arthrogryposis multiplex congenita (disorder)", "SYNE1 (spectrin repeat containing nuclear envelope protein 1) related arthrogryposis multiplex congenita"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive myogenic arthrogryposis multiplex congenita", "shortest_name_length": 17}
{"curie": "UMLS:C4724993", "names": ["Refractory Oropharyngeal Squamous Cell Carcinoma", "Refractory Oropharyngeal Throat Squamous Cell Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Oropharyngeal Squamous Cell Carcinoma", "shortest_name_length": 48}
{"curie": "MONDO:0011245", "names": ["HID syndrome", "HID Syndrome", "HID SYNDROME", "hystrix-like ichthyosis with deafness", "HYSTRIX-LIKE ICHTHYOSIS WITH DEAFNESS", "Hystrix-Like Ichthyosis with Deafness", "ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS", "ichthyosis, hystrix-like, with deafness", "Ichthyosis, Hystrix-Like, with Deafness", "ichthyosis, hystrix-like, with hearing loss"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ichthyosis, hystrix-like, with hearing loss", "shortest_name_length": 12}
{"curie": "MONDO:0003516", "names": ["Teratoma", "teratoma", "adult teratoma", "Adult Teratoma", "Adult teratoma", "teratoma of adults", "Adult teratoma, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult teratoma", "shortest_name_length": 8}
{"curie": "MONDO:0009602", "names": ["Roy Maroteaux Kremp syndrome", "metaphyseal modeling abnormality, skin lesions, and spastic paraplegia", "Metaphyseal modeling abnormality, skin lesions, and Spastic paraplegia", "METAPHYSEAL MODELING ABNORMALITY, SKIN LESIONS, AND SPASTIC PARAPLEGIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metaphyseal modeling abnormality, skin lesions, and spastic paraplegia", "shortest_name_length": 28}
{"curie": "MONDO:0032766", "names": ["Apolipoprotein A-I deficiency", "APOLIPOPROTEIN A-I DEFICIENCY", "Apolipoprotein A-I Deficiency", "primary hypoalphalipoproteinemia 2", "High Density Lipoprotein Deficiency", "HIGH DENSITY LIPOPROTEIN DEFICIENCY", "HYPOALPHALIPOPROTEINEMIA, PRIMARY, 2", "hypoalphalipoproteinemia, primary, 2", "ApoA-I and apoC-III deficiency, combined", "HYPOALPHALIPOPROTEINEMIA, PRIMARY, 2, AUTOSOMAL RECESSIVE", "hypoalphalipoproteinemia, primary, 2, with or without corneal clouding"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypoalphalipoproteinemia, primary, 2", "shortest_name_length": 29}
{"curie": "MONDO:0011695", "names": ["UVM1", "MELANOMA, UVEAL, SUSCEPTIBILITY TO, 1", "melanoma, uveal, susceptibility to, 1", "melanoma, uveal, susceptibility to, type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melanoma, uveal, susceptibility to, 1", "shortest_name_length": 4}
{"curie": "UMLS:C4683589", "names": ["Lugano Classification Stage IIE Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage IIE Hodgkin Lymphoma AJCC v8", "shortest_name_length": 56}
{"curie": "MONDO:0019855", "names": ["athyreosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "athyreosis", "shortest_name_length": 10}
{"curie": "MONDO:0015461", "names": ["Short rib polydactyly syndrome", "short rib-polydactyly syndrome", "Short Rib-Polydactyly Syndrome", "Short rib-polydactyly syndrome", "Short Rib Polydactyly Syndrome", "Short Rib-Polydactyly Syndromes", "Short rib polydactyly syndrome (disorder)", "Short rib polydactyly syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short rib-polydactyly syndrome", "shortest_name_length": 30}
{"curie": "MONDO:0015048", "names": ["amelogenesis imperfecta type 2", "Amelogenesis imperfecta type 2", "Hypomaturation amelogenesis imperfecta", "hypomaturation amelogenesis imperfecta", "Amelogenesis imperfecta - hypomaturation", "amelogenesis imperfecta hypomaturation type", "Amelogenesis Imperfecta hypomaturation type", "Amelogenesis imperfecta, hypomaturation type", "Amelogenesis imperfecta, hypomaturation type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amelogenesis imperfecta type 2", "shortest_name_length": 30}
{"curie": "UMLS:C0235328", "names": ["occlusion colon", "colon occlusion", "colon; occlusion", "occlusion; colon", "Obstruction colon", "colon obstruction", "obstruction colon", "COLON OBSTRUCTION", "OBSTRUCTION COLON", "Colon obstruction", "colon; obstruction", "Occlusion of colon", "colon obstructions", "obstruction; colon", "COLONIC OBSTRUCTION", "Colonic obstruction", "Colonic Obstruction", "colonic obstruction", "Obstruction of colon", "COLON NOS OBSTRUCTION", "colon obstruction (diagnosis)", "Obstruction of colon (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Obstruction of colon", "shortest_name_length": 15}
{"curie": "MONDO:0020131", "names": ["malformation of the cerebellar hemispheres"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malformation of the cerebellar hemispheres", "shortest_name_length": 42}
{"curie": "MONDO:0060527", "names": ["MHSA", "BHSA", "MAAID", "MAAI deficiency", "MAAI DEFICIENCY", "HYPERSUCCINYLACETONEMIA, MILD", "hypersuccinylacetonemia, mild", "BENIGN HYPERSUCCINYLACETONEMIA", "benign hypersuccinylacetonemia", "MALEYLACETOACETATE ISOMERASE DEFICIENCY", "maleylacetoacetate isomerase deficiency", "Deficiency of maleylacetoacetate isomerase", "Deficiency of maleylacetoacetate isomerase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maleylacetoacetate isomerase deficiency", "shortest_name_length": 4}
{"curie": "UMLS:C4683429", "names": ["Stage I Thyroid Gland Follicular Cancer 55 Years and Older", "Stage I Thyroid Gland Follicular Carcinoma 55 Years and Older AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Thyroid Gland Follicular Carcinoma 55 Years and Older AJCC v8", "shortest_name_length": 58}
{"curie": "MONDO:0017076", "names": ["posterior meningocele"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "posterior meningocele", "shortest_name_length": 21}
{"curie": "UMLS:C5204280", "names": ["Upper pole", "Upper Pole Kidney Tumor", "Kidney Tumor, Upper Pole"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kidney Tumor, Upper Pole", "shortest_name_length": 10}
{"curie": "MONDO:0032886", "names": ["LIWAS", "LIANG-WANG SYNDROME", "Liang-Wang syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liang-Wang syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C4055249", "names": ["Childhood AML with Abnormalities of Chromosome 7", "Acute Myeloid Leukemia (AML) with Abnormalities of Chromosome 7", "Childhood Acute Myeloid Leukemia with Abnormalities of Chromosome 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Acute Myeloid Leukemia with Abnormalities of Chromosome 7", "shortest_name_length": 48}
{"curie": "UMLS:C1516857", "names": ["EIC", "SEIC", "Endometrial Surface Serous Carcinoma", "Endometrial Serous Carcinoma in Situ", "Endometrial Intraepithelial Carcinoma", "Endometrial Serous Intraepithelial Carcinoma", "Serous endometrial intraepithelial carcinoma", "Serous Endometrial Intraepithelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Serous Endometrial Intraepithelial Carcinoma", "shortest_name_length": 3}
{"curie": "MONDO:0010332", "names": ["Cubitus Valgus with Mental Retardation and Unusual Facies", "cubitus valgus with mental retardation and unusual facies", "cubitus valgus with intellectual disability and unusual facies", "X-linked intellectual disability-cubitus valgus-dysmorphism syndrome", "CUBITUS VALGUS WITH IMPAIRED INTELLECTUAL DEVELOPMENT AND UNUSUAL FACIES", "Cubitus valgus with mental retardation and unusual facies, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability-cubitus valgus-dysmorphism syndrome", "shortest_name_length": 57}
{"curie": "MONDO:0004504", "names": ["penis urethra cancer", "penile urethral cancer", "urethra cancer of penis", "Penile Urethral Malignant Neoplasm", "penile urethral malignant neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "penile urethral cancer", "shortest_name_length": 20}
{"curie": "MONDO:0009341", "names": ["MOWS", "Mowat-Wilson syndrome", "MOWAT-WILSON SYNDROME", "Mowat-Wilson Syndrome", "Mowat-Wilson syndrome (disorder)", "Mowat-Wilson syndrome (diagnosis)", "Hirschsprung disease mental retardation syndrome", "HIRSCHSPRUNG DISEASE-MENTAL RETARDATION SYNDROME", "Hirschsprung disease-mental retardation syndrome", "Hirschsprung Disease-Mental Retardation Syndrome", "Hirschsprung disease intellectual disability syndrome", "Hirschsprung disease-intellectual disability syndrome", "microcephaly, mental retardation, and distinct facial featrues, with or without Hirschprung disease", "mental retardation, microcephaly, and distinct facial features with or without Hirschsprung disease", "Microcephaly, Mental Retardation, and Distinct Facial Features, with Or without Hirschsprung Disease", "microcephaly, mental retardation, and distinct Facial features, with or without Hirschsprung disease", "MICROCEPHALY, MENTAL RETARDATION, AND DISTINCT FACIAL FEATURES, WITH OR WITHOUT HIRSCHSPRUNG DISEASE", "intellectual disability, microcephaly, and distinct facial features with or without Hirschsprung disease", "microcephaly, intellectual disability, and distinct facial featrues, with or without Hirschprung disease", "microcephaly, intellectual disability, and distinct Facial features, with or without Hirschsprung disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mowat-Wilson syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0740421", "names": ["Surgical menopause", "Surgical Menopause", "MENOPAUSE SURGICAL", "surgical menopause", "menopause surgical", "surgical; menopausal", "menopausal; surgical", "Postsurgical menopause", "Postsurgical menopause (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postsurgical menopause", "shortest_name_length": 18}
{"curie": "MONDO:0002234", "names": ["colpitis", "Colpitis", "Vaginitis", "VAGINITIS", "vaginitis", "Vaginitides", "Vaginitis NOS", "Vulvovaginitis", "Vaginitis, NOS", "irritation; vagina", "vagina; irritation", "inflammation vagina", "Inflammation;vagina", "vaginitis (disease)", "vagina inflammation", "Vaginal Inflammation", "vaginal Inflammation", "vagina; inflammation", "inflammation; vagina", "Vaginitis (disorder)", "Vaginal inflammation", "vaginal inflammation", "inflammation vaginal", "vaginitis (diagnosis)", "Inflammation of vagina", "inflammation of vagina", "inflammation of the vagina", "Vaginitis and vulvovaginitis", "vaginitis and vulvovaginitis", "vaginitis and vulvovaginitis (diagnosis)", "Vaginitis and vulvovaginitis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vaginitis", "shortest_name_length": 8}
{"curie": "MONDO:0009987", "names": ["Pericentral retinitis pigmentosa", "retinitis pigmentosa, pericentral", "RETINITIS PIGMENTOSA, PERICENTRAL", "Retinitis Pigmentosa, Pericentral", "autosomal recessive pericentral pigmentary retinopathy", "Retinopathy, Pericentral Pigmentary, Autosomal Recessive", "retinopathy, pericentral pigmentary, autosomal recessive", "RETINOPATHY, PERICENTRAL PIGMENTARY, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive pericentral pigmentary retinopathy", "shortest_name_length": 32}
{"curie": "MONDO:0004465", "names": ["periampullary cancer", "periampullary adenocarcinoma", "Periampullary Adenocarcinoma", "Periampullary adenocarcinoma", "periampullary region of duodenum adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "periampullary adenocarcinoma", "shortest_name_length": 20}
{"curie": "UMLS:C0027667", "names": ["occult primary tumor", "cancer origin unknown", "cancer unknown primary", "cancer primary unknown", "unknown primary cancer", "Unknown primary cancer", "cancer, unknown primary", "Cancer - unknown origin", "Occult Primary Neoplasm", "Occult Primary Neoplasms", "Unknown Primary Neoplasm", "Neoplasm, Occult Primary", "Primary Neoplasm, Occult", "Unknown Primary Neoplasms", "Primary Neoplasms, Occult", "Neoplasms, Occult Primary", "Primary Neoplasm, Unknown", "Neoplasm, Unknown Primary", "Primary Neoplasms, Unknown", "Neoplasms, Unknown Primary", "Metastasis - unknown primary", "metastasis of unknown primary", "CA - Cancer of unknown origin", "Cancer of Unknown Primary Site", "cancer of unknown primary origin", "Malignant tumor - unknown primary", "Malignant tumor of unknown origin", "Malignant tumour of unknown origin", "Malignant tumour - unknown primary", "Malignant neoplasm of unknown origin", "malignant neoplasm of unknown origin", "metastatic carcinoma of unknown primary", "UKP - Malignant tumor - unknown primary", "UKP - Malignant tumour - unknown primary", "metastasis of unknown primary (diagnosis)", "Metastatic Neoplasm of Unknown Primary Origin", "Metastatic neoplasm NOS, primary site unknown", "Malignant neoplasm of unknown origin (disorder)", "Metastatic Malignant Neoplasm of Unknown Primary", "malignant neoplasm of unknown origin (diagnosis)", "metastatic malignant neoplasm of unknown primary origin", "Metastatic Malignant Neoplasm of Unknown Primary Origin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplasms, Unknown Primary", "shortest_name_length": 20}
{"curie": "MONDO:0022576", "names": ["bilirubin induced brain injury in the newborn"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bilirubin induced brain injury in the newborn", "shortest_name_length": 45}
{"curie": "UMLS:C4525724", "names": ["Nuclear Cataract Grade 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nuclear Cataract Grade 2", "shortest_name_length": 24}
{"curie": "MONDO:0019101", "names": ["retinal capillary malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal capillary malformation", "shortest_name_length": 30}
{"curie": "UMLS:C0555305", "names": ["minor head injury", "Minor head injury", "head injury minor", "Minor Head Injury", "Injury, Minor Head", "Head Injury, Minor", "Minor Head Injuries", "Head Injuries, Minor", "Injuries, Minor Head", "HEAD INJURY TRAUMA MINOR", "Minor head injury (disorder)", "minor head injury (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Head Injury, Minor", "shortest_name_length": 17}
{"curie": "UMLS:C3898279", "names": ["Moderate BPD", "Moderate Bronchopulmonary Dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Moderate Bronchopulmonary Dysplasia", "shortest_name_length": 12}
{"curie": "UMLS:C5670688", "names": ["Melanocytoma of Intermediate Grade", "Meningeal Melanocytoma of Intermediate Grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meningeal Melanocytoma of Intermediate Grade", "shortest_name_length": 34}
{"curie": "MONDO:0006166", "names": ["CCH", "Breast Columnar Cell Hyperplasia", "Columnar Cell Hyperplasia of Breast", "columnar cell hyperplasia of breast", "columnar cell hyperplasia of the breast", "Columnar Cell Hyperplasia of the Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "columnar cell hyperplasia of the breast", "shortest_name_length": 3}
{"curie": "UMLS:C0741983", "names": ["CAROTID SINUS HYPERSENSITIVITY", "Carotid sinus hypersensitivity", "hypersensitivity; carotid sinus", "carotid sinus; hypersensitivity", "sinus caroticus; hypersensitivity", "Carotid sinus hypersensitivity (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carotid sinus hypersensitivity", "shortest_name_length": 30}
{"curie": "MONDO:0022333", "names": ["5'NT syndrome", "5-nucleotidase syndrome", "5-Nucleotidase syndrome", "5'-Nucleotidase syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "5-nucleotidase syndrome", "shortest_name_length": 13}
{"curie": "UMLS:C1332549", "names": ["bilateral cancer", "Bilateral Cancer", "Bilateral Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bilateral Carcinoma", "shortest_name_length": 16}
{"curie": "MONDO:0001739", "names": ["Purulent labyrinthitis", "purulent labyrinthitis", "bacterial labyrinthitis", "Suppurative labyrinthitis", "labyrinthitis suppurative", "suppurative labyrinthitis", "acute suppurative labyrinthitis", "Suppurative labyrinthitis (disorder)", "suppurative labyrinthitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "purulent labyrinthitis", "shortest_name_length": 22}
{"curie": "UMLS:C1096260", "names": ["Enterococcal sepsis", "Enterococcal septicemia", "septicemia enterococcal", "Enterococcal septicaemia", "septicemia enterococcal (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Enterococcal sepsis", "shortest_name_length": 19}
{"curie": "MONDO:0043759", "names": ["Abdominal Pregnancy", "abdominal pregnancy", "Abdominal pregnancy", "Pregnancy, Abdominal", "Pregnancy, abdominal", "PREGNANCY, ABDOMINAL", "abdominal; pregnancy", "pregnancy; abdominal", "Abdominal Pregnancies", "abdominal Pregnancies", "Pregnancies, Abdominal", "Pregnancies, abdominal", "Abdominal pregnancy NOS", "Intra-abdominal Pregnancy", "abdomen ectopic pregnancy", "intra-abdominal pregnancy", "abdominal ectopic pregnancy", "ectopic pregnancy of abdomen", "Abdominal pregnancy (disorder)", "abdominal pregnancy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "abdominal ectopic pregnancy", "shortest_name_length": 19}
{"curie": "MONDO:0003263", "names": ["childhood cerebellar tumor", "Pediatric Cerebellar Tumor", "Childhood Cerebellar Tumor", "pediatric cerebellar tumor", "Childhood Cerebellar Tumors", "childhood cerebellar tumors", "childhood tumor of cerebellum", "childhood cerebellar neoplasm", "pediatric tumor of Cerebellum", "Childhood Tumor of Cerebellum", "Pediatric Cerebellar Neoplasm", "Childhood Cerebellar Neoplasm", "Pediatric Tumor of Cerebellum", "pediatric cerebellar neoplasm", "pediatric tumor of cerebellum", "childhood cerebellar neoplasms", "Childhood Cerebellar Neoplasms", "Pediatric Neoplasm of Cerebellum", "childhood neoplasm of cerebellum", "Childhood Neoplasm of Cerebellum", "pediatric neoplasm of cerebellum", "Childhood Tumor of the Cerebellum", "Pediatric Tumor of the Cerebellum", "childhood tumor of the cerebellum", "pediatric tumor of the cerebellum", "childhood neoplasm of the cerebellum", "pediatric neoplasm of the cerebellum", "Childhood Neoplasm of the Cerebellum", "Pediatric Neoplasm of the Cerebellum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood cerebellar neoplasm", "shortest_name_length": 26}
{"curie": "MONDO:0007096", "names": ["Ahumada-del Castillo", "Nonpuerperal galactorrhea", "Argonz-Del Castillo Syndrome", "Argonz-Del Castillo syndrome", "Ahumada-del Castillo syndrome", "Ahumada-Del Castillo syndrome", "ahumada-del castillo syndrome", "amenorrhea-galactorrhea syndrome", "Amenorrhea-galactorrhea syndrome", "AMENORRHEA-GALACTORRHEA SYNDROME", "non-pregnancy related A-G syndrome", "Amenorrhoea-galactorrhoea syndrome", "Non-pregnancy related A-G syndrome", "Argonz-Ahumada-Del Castillo syndrome", "Amenorrhea-galactorrhea syndrome, NOS", "Amenorrhea-hyperprolactinemia syndrome", "Amenorrhoea-galactorrhoea syndrome, NOS", "Non-pregnancy related A-G syndrome, NOS", "Amenorrhoea-hyperprolactinaemia syndrome", "Amenorrhea-Galactorrhea-FSH Decrease Syndrome", "Non-pregnancy related A-G syndrome (disorder)", "non-pregnancy related A-G syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amenorrhea-galactorrhea syndrome", "shortest_name_length": 20}
{"curie": "MONDO:0020580", "names": ["germinomatous germ cell tumor", "Germinomatous Germ Cell Tumor", "Seminoma/Dysgerminoma/Germinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "germinomatous germ cell tumor", "shortest_name_length": 29}
{"curie": "MONDO:0800112", "names": ["non-atopic asthma", "instrinsic asthma", "non-allergic asthma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-atopic asthma", "shortest_name_length": 17}
{"curie": "MONDO:0032811", "names": ["CSNB1I", "night blindness, congenital stationary, type1i", "NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE1I", "night blindness, congenital stationary, type 1I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "night blindness, congenital stationary, type1i", "shortest_name_length": 6}
{"curie": "MONDO:0800153", "names": ["urea cycle disorder or inherited hyperammonemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urea cycle disorder or inherited hyperammonemia", "shortest_name_length": 47}
{"curie": "MONDO:0012069", "names": ["KTCN3", "keratoconus 3", "KERATOCONUS 3", "Keratoconus 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratoconus 3", "shortest_name_length": 5}
{"curie": "UMLS:C4524709", "names": ["Gastroesophageal Junction Adenocarcinoma by AJCC v8 cTNM Stage", "Gastroesophageal Junction Adenocarcinoma by AJCC v8 Clinical Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastroesophageal Junction Adenocarcinoma by AJCC v8 Clinical Stage", "shortest_name_length": 62}
{"curie": "MONDO:0008027", "names": ["muscular atrophy, malignant neurogenic", "Muscular Atrophy, Malignant Neurogenic", "MUSCULAR ATROPHY, MALIGNANT NEUROGENIC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular atrophy, malignant neurogenic", "shortest_name_length": 38}
{"curie": "MONDO:0008211", "names": ["Patterson syndrome", "Patterson's leprechaunoid syndrome", "PATTERSON PSEUDOLEPRECHAUNISM SYNDROME", "Patterson pseudoleprechaunism syndrome", "Pseudoleprechaunism syndrome Patterson type", "pseudoleprechaunism syndrome, Patterson type", "Pseudoleprechaunism syndrome, Patterson type", "Pseudoleprechaunism syndrome Patterson type (disorder)", "pseudoleprechaunism syndrome, Patterson type (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudoleprechaunism syndrome, Patterson type", "shortest_name_length": 18}
{"curie": "MONDO:0013925", "names": ["MAHCJ", "CblJ defects", "cblJ defects", "Cobalamin J defect", "cobalamin J defect", "METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE", "methylmalonic aciduria and homocystinuria, cblJ type", "Methylmalonic Aciduria and Homocystinuria, cblJ Type", "methylmalonic acidemia with homocystinuria type cblJ", "methylmalonic aciduria with homocystinuria, type cblJ", "Methylmalonic aciduria with homocystinuria, type cblJ", "Methylmalonic acidemia with homocystinuria, type cblJ", "methylmalonic acidemia with homocystinuria, type cblJ", "combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblJ", "Combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblJ"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "methylmalonic acidemia with homocystinuria, type cblJ", "shortest_name_length": 5}
{"curie": "MONDO:0021357", "names": ["salivary gland tumor", "Salivary Gland Tumor", "Salivary Gland Neoplasm", "tumor of salivary gland", "Tumor of Salivary Gland", "salivary gland neoplasm", "Neoplasm of Salivary Gland", "neoplasm of salivary gland", "tumor of the salivary gland", "Tumor of the Salivary Gland", "saliva-secreting gland tumor", "neoplasm of the salivary gland", "Neoplasm of the Salivary Gland", "tumor of saliva-secreting gland", "saliva-secreting gland neoplasm", "Mixed Tumor of the Salivary Gland", "neoplasm of saliva-secreting gland", "saliva-secreting gland neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tumor of salivary gland", "shortest_name_length": 20}
{"curie": "MONDO:0010786", "names": ["Chronic diarrhea with villous atrophy", "chronic diarrhea with villous atrophy", "DIARRHEA, CHRONIC, WITH VILLOUS ATROPHY", "diarrhea, chronic, with villous atrophy", "Diarrhea, Chronic, with Villous Atrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic diarrhea with villous atrophy", "shortest_name_length": 37}
{"curie": "MONDO:0019040", "names": ["Chromosomopathy", "chromosome anomaly", "anomaly chromosomal", "chromosome disorder", "chromosome; anomaly", "CHROMOSOME DISORDER", "Chromosome disorder", "Chromosome Disorder", "chromosomal disease", "Chromosomal anomaly", "chromosomal diseases", "Chromosomal disorder", "chromosome disorders", "Disorder, Chromosome", "anomaly; chromosomes", "abnormal chromosomes", "abnormal; chromosome", "CHROMOSOMAL DISEASES", "anomalies chromosome", "chromosome; abnormal", "disorder, chromosome", "chromosomes disorder", "diseases chromosomal", "Chromosomopathy, NOS", "chromosomal disorder", "Chromosomal Disorder", "disorders chromosome", "Chromosome Disorders", "Disorder, Chromosomal", "chromosomes disorders", "chromosomal anomalies", "disorder, chromosomal", "Anomaly of chromosome", "chromosomal disorders", "Disorders, Chromosome", "anomalies chromosomes", "Chromosomal anomalies", "disorders, chromosome", "Chromosomal Disorders", "Chromosomal disorders", "CHROMOSOME ABNORMALITY", "abnormality chromosome", "chromosome abnormality", "Disorders, Chromosomal", "disorders, chromosomal", "Abnormal;chromosome(s)", "Chromosome abnormality", "abnormality chromosomal", "Chromosomal abnormality", "chromosomal abnormality", "Cytogenetic abnormality", "Chromosomal Abnormality", "Chromosomal disease, NOS", "abnormalities chromosomes", "Anomaly of chromosome, NOS", "Chromosomal abnormality NOS", "autosomal chromosome disorder", "autosomal chromosome disorders", "Congenital chromosomal disease", "chromosome disorder, autosomal", "Chromosomal imbalance syndrome", "chromosome abnormality disorder", "Chromosome Abnormality Disorder", "Chromosomal disorder (disorder)", "chromosome disorders, autosomal", "Chromosomal hereditary disorder", "Chromosomal disease or syndrome", "Disorder, Chromosome Abnormality", "disorder, chromosome abnormality", "Chromosomal abnormality syndrome", "Chromosome Abnormality Disorders", "chromosome abnormality disorders", "chromosomal anomalies (diagnosis)", "Chromosomal Diseases and Syndromes", "Chromosomal imbalance syndrome, NOS", "Chromosomal hereditary disorder, NOS", "Chromosomal abnormality, unspecified", "Chromosomal abnormality syndrome, NOS", "Conditions due to anomaly of unspecified chromosome", "Congenital disorder due to abnormality of chromosome number OR structure", "Congenital disorder due to abnormality of chromosome number OR structure (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosomal disorder", "shortest_name_length": 15}
{"curie": "UMLS:C0278877", "names": ["Meningioma", "adult meningioma", "Adult Meningioma", "meningioma, adult", "adult CNS tumor, meningioma", "CNS tumor, adult meningioma", "CNS tumor, meningioma, adult", "adult brain tumor, meningioma", "brain tumor, adult meningioma", "brain tumor, meningioma, adult", "central nervous system tumor, meningioma, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Meningioma", "shortest_name_length": 10}
{"curie": "UMLS:C0751005", "names": ["Intracranial Mycotic Aneurysm", "Intracranial Mycotic Aneurysms", "Mycotic Aneurysm, Intracranial", "Aneurysm, Intracranial Mycotic", "Mycotic Aneurysms, Intracranial", "Aneurysms, Intracranial Mycotic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mycotic Aneurysm, Intracranial", "shortest_name_length": 29}
{"curie": "MONDO:0019054", "names": ["congenital limb malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital limb malformation", "shortest_name_length": 28}
{"curie": "UMLS:C3826462", "names": ["Depression in children"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Depression in children", "shortest_name_length": 22}
{"curie": "UMLS:C1334712", "names": ["Metastatic Benign Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Benign Neoplasm", "shortest_name_length": 26}
{"curie": "MONDO:0001064", "names": ["acute otosalpingitis", "otosalpingitis, acute", "Acute Eustachian salpingitis", "Acute eustachian salpingitis", "acute eustachian salpingitis", "Acute eustachian tube salpingitis", "acute eustachian tube salpingitis", "acute eustachian salpingitis (diagnosis)", "Acute eustachian tube salpingitis (disorder)", "Acute Eustachian salpingitis, unspecified ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute eustachian salpingitis", "shortest_name_length": 20}
{"curie": "MONDO:0009143", "names": ["EPS", "MGORS1", "MEIER-GORLIN SYNDROME", "Meier-Gorlin syndrome", "Meier-GORLIN syndrome 1", "Meier-Gorlin syndrome 1", "MEIER-GORLIN SYNDROME 1", "ORC1 Meier-Gorlin syndrome", "Meier-Gorlin syndrome type 1", "Ear-patella-short stature syndrome", "EAR, PATELLA, SHORT STATURE SYNDROME", "Ear, patella, short stature syndrome", "Ear, patella, short stature syndrome (disorder)", "Microtia, absent patellae, micrognathia syndrome", "MICROTIA, ABSENT PATELLAE, MICROGNATHIA SYNDROME", "microtia, absent patellae, micrognathia syndrome", "Meier-Gorlin syndrome caused by mutation in ORC1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meier-Gorlin syndrome 1", "shortest_name_length": 3}
{"curie": "MONDO:0017041", "names": ["osteochondrodysplatic nanism-deafness-retinitis pigmentosa syndrome", "Osteochondrodysplatic nanism-deafness-retinitis pigmentosa syndrome", "Osteochondrodysplatic dwarfism-deafness-retinitis pigmentosa syndrome", "Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome", "Osteochondrodysplatic nanism-hearing loss-retinitis pigmentosa syndrome", "Osteochondrodysplatic dwarfism-hearing loss-retinitis pigmentosa syndrome", "Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteochondrodysplatic nanism-deafness-retinitis pigmentosa syndrome", "shortest_name_length": 67}
{"curie": "UMLS:C0237123", "names": ["AOD use", "Substance use", "substance use", "Substance Use", "substances use", "Substance Uses", "Use, Substance", "alcohol drug use", "drug alcohol use", "alcohol drugs use", "Alcohol - drug use", "use (alcohol, drug)", "Alcohol or Other Drugs use", "alcohol and other drug use"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alcohol or Other Drugs use", "shortest_name_length": 7}
{"curie": "MONDO:0017508", "names": ["Adactyly of hand, bilateral", "digits 2-5 hypodactyly, bilateral", "digits 2-5 oligodactyly, bilateral", "congenital absence/hypoplasia of fingers excluding thumb, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital absence/hypoplasia of fingers excluding thumb, bilateral", "shortest_name_length": 27}
{"curie": "UMLS:C4726552", "names": ["Myeloid Neoplasms with Germline ETV6 Mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myeloid Neoplasms with Germline ETV6 Mutation", "shortest_name_length": 45}
{"curie": "UMLS:C0333988", "names": ["Pseudocarcinomatous hyperplasia", "pseudocarcinomatous hyperplasia", "hyperplasia pseudoepitheliomatous", "Pseudoepitheliomatous Hyperplasia", "Pseudoepitheliomatous hyperplasia", "Hyperplasia, pseudoepitheliomatous", "Pseudoepitheliomatous hyperplasia (disorder)", "Pseudoepitheliomatous hyperplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pseudoepitheliomatous hyperplasia", "shortest_name_length": 31}
{"curie": "MONDO:0012568", "names": ["OS4", "GOA1", "OSTEOARTHRITIS SUSCEPTIBILITY 4", "osteoarthritis susceptibility 4", "osteoarthritis, generalized, without dysplasia", "OSTEOARTHRITIS, GENERALIZED, WITHOUT DYSPLASIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteoarthritis susceptibility 4", "shortest_name_length": 3}
{"curie": "UMLS:C1335774", "names": ["Retroperitoneal Disease", "Retroperitoneal disorder", "Retroperitoneal Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retroperitoneal disorder", "shortest_name_length": 23}
{"curie": "UMLS:C0854823", "names": ["Anaplastic Large Cell Lymphoma Stage II", "Stage II Anaplastic Large Cell Lymphoma", "Ann Arbor Stage II Anaplastic Large Cell Lymphoma", "Anaplastic Large Cell Lymphoma T- and Null-Cell Types Stage II", "Anaplastic large cell lymphoma T- and null-cell types stage II", "Ann Arbor Stage II Noncutaneous Anaplastic Large Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Anaplastic Large Cell Lymphoma", "shortest_name_length": 39}
{"curie": "UMLS:C3665858", "names": ["Parenteral nutrition associated liver disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parenteral nutrition associated liver disease", "shortest_name_length": 45}
{"curie": "MONDO:0013630", "names": ["MKS9", "meckel syndrome 9", "B9D1 Meckel syndrome", "Meckel syndrome type 9", "MECKEL SYNDROME, TYPE 9", "Meckel syndrome, type 9", "Meckel syndrome type 9 (diagnosis)", "Meckel syndrome caused by mutation in B9D1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meckel syndrome, type 9", "shortest_name_length": 4}
{"curie": "MONDO:0014181", "names": ["ALS20", "ALS20 (diagnosis)", "AMYOTROPHIC LATERAL SCLEROSIS 20", "amyotrophic lateral sclerosis 20", "amyotrophic lateral sclerosis ALS20", "amyotrophic lateral sclerosis type 20", "HNRNPA1 amyotrophic lateral sclerosis", "amyotrophic lateral sclerosis caused by mutation in HNRNPA1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyotrophic lateral sclerosis type 20", "shortest_name_length": 5}
{"curie": "MONDO:0018847", "names": ["Vitelline duct cyst", "omphalomesenteric cyst", "Omphalomesenteric cyst", "Omphalomesenteric duct cyst", "omphalomesenteric duct cyst", "Congenital umbilical granuloma", "Omphalomesenteric duct cyst (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "omphalomesenteric cyst", "shortest_name_length": 19}
{"curie": "MONDO:0019693", "names": ["multiple metaphyseal dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple metaphyseal dysplasia", "shortest_name_length": 30}
{"curie": "UMLS:C5670680", "names": ["Stage IIIA Cervical Cancer FIGO 2009", "Stage IIIA Cervical Carcinoma FIGO 2009"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Cervical Cancer FIGO 2009", "shortest_name_length": 36}
{"curie": "MONDO:0008272", "names": ["CP1", "PPD4", "polysyndactyly 4", "polydactyly preaxial 4", "preaxial polydactyly 4", "Polydactyly, preaxial 4", "polydactyly, preaxial 4", "Polydactyly, Preaxial Iv", "POLYDACTYLY, PREAXIAL IV", "polydactyly, preaxial IV", "crossed polydactyly type 1", "CROSSED POLYDACTYLY, TYPE I", "preaxial polydactyly type 4", "Crossed Polydactyly, Type I", "crossed polydactyly, type 1", "polysyndactyly uncomplicated", "polydactyly, preaxial type 4", "POLYSYNDACTYLY, UNCOMPLICATED", "polysyndactyly, uncomplicated", "Polysyndactyly, uncomplicated", "polydactyly, preaxial, type IV"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polysyndactyly 4", "shortest_name_length": 3}
{"curie": "UMLS:C0342938", "names": ["Pantothenic acid deficiency", "acid deficiency pantothenic", "pantothenic acid deficiency", "deficiency; pantothenic acid", "pantothenic acid; deficiency", "Deficiency of pantothenic acid", "Pantothenic acid deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pantothenic acid deficiency", "shortest_name_length": 27}
{"curie": "UMLS:C2981368", "names": ["Stage IA Esophageal Squamous Cell Cancer", "Stage IA Esophageal Squamous Cell Carcinoma", "Stage IA Esophageal Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Esophageal Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 40}
{"curie": "MONDO:0003121", "names": ["Middle Cranial Fossa Meningioma", "middle cranial fossa meningioma", "meningioma of middle cranial fossa", "Meningioma of Middle Cranial Fossa", "meningioma of the middle Cranial Fossa", "meningioma of the middle cranial fossa", "Meningioma of the Middle Cranial Fossa", "middle cranial fossa meningioma (disease)", "meningioma (disease) of middle cranial fossa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "middle cranial fossa meningioma", "shortest_name_length": 31}
{"curie": "UMLS:C0917813", "names": ["Open spina bifida", "Open Spina Bifida", "open spina bifida", "spina bifida open", "Spina Bifida, Open"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spina Bifida, Open", "shortest_name_length": 17}
{"curie": "UMLS:C4523931", "names": ["Sedation complication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sedation complication", "shortest_name_length": 21}
{"curie": "MONDO:0016671", "names": ["HbSE disease", "sickle cell-hemoglobin E disease syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sickle cell-hemoglobin E disease syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0033181", "names": ["phenytoin or carbamazepine toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phenytoin or carbamazepine toxicity", "shortest_name_length": 35}
{"curie": "MONDO:0033565", "names": ["OOMD9", "oocyte maturation defect 9", "OOCYTE MATURATION DEFECT 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oocyte maturation defect 9", "shortest_name_length": 5}
{"curie": "UMLS:C4683581", "names": ["Lugano Classification Advanced Stage Adult Non-Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Advanced Stage Adult Non-Hodgkin Lymphoma AJCC v8", "shortest_name_length": 71}
{"curie": "UMLS:C0340726", "names": ["embolism vein", "vein embolism", "vein; embolism", "embolism; vein", "venous embolism", "Venous embolism", "Embolism venous", "Embolus of vein", "Venous Embolism", "Embolism of vein", "Venous embolism NOS", "Embolism of vein NOS", "Venous embolism (disorder)", "venous embolism (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Venous embolism", "shortest_name_length": 13}
{"curie": "UMLS:C0016385", "names": ["Flutter", "flutter", "flutters", "fluttering", "Cardiac flutter", "Cardiac Flutter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiac Flutter", "shortest_name_length": 7}
{"curie": "MONDO:0025506", "names": ["postweaning multisystemic wasting syndrome", "porcine postweaning multisystemic wasting syndrome", "Porcine Postweaning Multisystemic Wasting Syndrome", "Postweaning Multisystemic Wasting Syndrome, Porcine", "postweaning multisystemic wasting syndrome, porcine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "porcine postweaning multisystemic wasting syndrome", "shortest_name_length": 42}
{"curie": "MONDO:0009393", "names": ["HHH", "HHHS", "Hhh syndrome", "HHH syndrome", "HHH SYNDROME", "ORNT1 deficiency", "Triple H syndrome", "triple H syndrome", "Triple H Syndrome", "ornithine carrier deficiency", "Ornithine carrier deficiency", "ORNITHINE TRANSLOCASE DEFICIENCY", "ornithine translocase deficiency", "Ornithine translocase deficiency", "ornithine translocase deficiency syndrome", "Hyperornithinemia-hyperammonemia-homocitrullinuria", "Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome", "hyperornithinemia-hyperammonemia-homocitrullinemia syndrome", "Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome", "Hyperammonemia-Hyperornithinemia-Homocitrullinemia syndrome", "hyperammonemia-hyperornithinemia-homocitrullinemia syndrome", "HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME", "hyperornithinemia-hyperammonemia-homocitrullinuria syndrome", "Hyperornithinemia-Hyperammonemia-Homocitrullinemia Syndrome", "Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome", "hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome", "HHH - Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome", "Hyperornithinemia-Hyperammonemia-Homocitrullinuria (HHH) syndrome", "HHH - Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome", "Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome (disorder)", "hyperammonemia-hyperornithinemia-homocitrullinemia syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ornithine translocase deficiency", "shortest_name_length": 3}
{"curie": "MONDO:0007839", "names": ["AASE-SMITH SYNDROME", "Aase Smith syndrome", "Aase-Smith syndrome", "Aase-Smith Syndrome I", "Aase-Smith I syndrome", "Aase Smith I syndrome", "Aase-Smith syndrome I", "Aase-Smith syndrome 1", "AASE-SMITH SYNDROME I", "Aase-Smith syndrome type 1", "Aase Smith type 1 syndrome", "JOINT CONTRACTURES WITH OTHER ABNORMALITIES", "Joint contractures with Other abnormalities", "Joint contractures with other abnormalities", "Hydrocephalus cleft palate joint contractures", "Hydrocephalus-cleft palate-joint contractures syndrome", "hydrocephalus-cleft palate-joint contractures syndrome", "Hydrocephalus with cleft palate and joint contracture syndrome", "Hydrocephalus with cleft palate and joint contracture syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aase-Smith syndrome", "shortest_name_length": 19}
{"curie": "MONDO:0007628", "names": ["FVH1", "foveal hypoplasia 1", "FOVEAL HYPOPLASIA 1", "PAX6 foveal hypoplasia", "foveal hypoplasia type 1", "O Donnell Pappas syndrome", "foveal hypoplasia, presenile cataract", "foveal hypoplasia caused by mutation in PAX6", "foveal hypoplasia 1 with or without anterior segment anomalies and/or cataract", "FOVEAL HYPOPLASIA 1 WITH OR WITHOUT ANTERIOR SEGMENT ANOMALIES AND/OR CATARACT", "foveal hypoplasia, congenital nystagmus, corneal pannus, and presenile cataracts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "foveal hypoplasia 1", "shortest_name_length": 4}
{"curie": "UMLS:C5556714", "names": ["Human Papillomavirus-Related Vaginal Squamous Cell Carcinoma", "Human Papillomavirus-Associated Vaginal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Human Papillomavirus-Related Vaginal Squamous Cell Carcinoma", "shortest_name_length": 60}
{"curie": "UMLS:C1710402", "names": ["MALT Lymphoma of the Mediastinum", "Primary Thymic Extranodal Marginal Zone Lymphoma", "Thymic Mucosa-Associated Lymphoid Tissue Lymphoma", "Mediastinal Mucosa-Associated Lymphoid Tissue Lymphoma", "Thymic Extranodal Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thymic Mucosa-Associated Lymphoid Tissue Lymphoma", "shortest_name_length": 32}
{"curie": "MONDO:0013222", "names": ["MMD3", "Miyoshi myopathy 3", "Miyoshi Myopathy 3", "MIYOSHI MYOPATHY 3", "Distal anoctaminopathy", "distal anoctaminopathy", "Miyoshi Muscular Dystrophy 3", "MIYOSHI MUSCULAR DYSTROPHY 3", "Miyoshi muscular dystrophy 3", "Distal anoctaminopathy (disorder)", "Miyoshi muscular dystrophy type 3", "MMD3 - Miyoshi muscular dystrophy type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Miyoshi muscular dystrophy 3", "shortest_name_length": 4}
{"curie": "MONDO:0007364", "names": ["Contractures of fingers and jaw", "CONTRACTURES OF FINGERS AND JAW", "arthrogryposis, distal, type 2E", "ARTHROGRYPOSIS, DISTAL, TYPE 2E", "contractures of fingers and jaw", "Arthrogryposis, distal, type 2E"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis, distal, type 2E", "shortest_name_length": 31}
{"curie": "UMLS:C4525205", "names": ["IIIB", "Stage IIIB Hepatocellular Cancer", "Stage IIIB Liver Cell Carcinoma AJCC v8", "Stage IIIB Hepatocellular Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Hepatocellular Carcinoma AJCC v8", "shortest_name_length": 4}
{"curie": "MONDO:0011185", "names": ["CDB2", "CDTB", "TBCD", "Honeycomb corneal dystrophy", "honeycomb corneal dystrophy", "curly fiber corneal dystrophy", "Curly fiber corneal dystrophy", "corneal dystrophy Thiel-Behnke", "Thiel Behnke corneal dystrophy", "THIEL-BEHNKE CORNEAL DYSTROPHY", "Thiel-Behnke corneal dystrophy", "Corneal dystrophy honeycomb-shaped", "corneal dystrophy honeycomb-shaped", "corneal dystrophy honeycomb shaped", "corneal dystrophy Thiel Behnke type", "CORNEAL DYSTROPHY, HONEYCOMB-SHAPED", "corneal dystrophy, honeycomb-Shaped", "Corneal Dystrophy, Honeycomb-Shaped", "corneal dystrophy, Thiel-Behnke type", "Corneal dystrophy, Thiel-Behnke type", "CORNEAL DYSTROPHY, THIEL-BEHNKE TYPE", "Waardenburg-Jonker corneal dystrophy", "corneal dystrophy of Bowman layer type 2", "Corneal dystrophy of Bowman layer type 2", "Thiel-Behnke corneal dystrophy (disorder)", "corneal dystrophy of Bowman Layer, type 2", "corneal dystrophy of Bowman layer type II", "Corneal dystrophy of Bowman layer type II", "Thiel-Behnke corneal dystrophy (diagnosis)", "Corneal Dystrophy Of Bowman Layer, Type II", "CORNEAL DYSTROPHY OF BOWMAN LAYER, TYPE II", "anterior limiting membrane dystrophy type 2", "Anterior limiting membrane dystrophy type 2", "Anterior limiting membrane dystrophy type II", "anterior limiting membrane dystrophy type II", "corneal dystrophy of the Bowman layer type 2", "Corneal dystrophy of the Bowman layer, type 2", "CDB type II-Corneal dystrophy of Bowman's membrane, type II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thiel-Behnke corneal dystrophy", "shortest_name_length": 4}
{"curie": "MONDO:0011305", "names": ["CCM3", "cerebral cavernous malformation 3", "cerebral cavernous malformations-3", "CEREBRAL CAVERNOUS MALFORMATIONS 3", "cerebral cavernous malformations 3", "Cerebral Cavernous Malformations 3", "cerebral cavernous malformation type 3", "cerebral cavernous malformations type 3", "PDCD10 familial cerebral cavernous malformation", "familial cerebral cavernous malformation caused by mutation in PDCD10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral cavernous malformation 3", "shortest_name_length": 4}
{"curie": "UMLS:C0740409", "names": ["Psychotic behavior", "behavior psychotic", "BEHAVIOR PSYCHOTIC", "psychotic behavior", "Psychotic behaviour"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Psychotic behavior", "shortest_name_length": 18}
{"curie": "UMLS:C5419777", "names": ["Intestinal Neuroendocrine Tumor G3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal Neuroendocrine Tumor G3", "shortest_name_length": 34}
{"curie": "MONDO:0016030", "names": ["Evans", "EVAN SYNDROME", "Evan syndrome", "evan syndrome", "evans syndrome", "Evans syndrome", "Evans Syndrome", "Evans' Syndrome", "evan's syndrome", "Evans' syndrome", "evans' syndrome", "evans's syndrome", "Immune pancytopenia", "immune pancytopenia", "Evans syndrome (disorder)", "Evans' syndrome (diagnosis)", "autoimmune hemolytic anemia and autoimmune thrombocytopenia", "Autoimmune hemolytic anemia and autoimmune thrombocytopenia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Evans syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C3272409", "names": ["Gastric NEC", "Gastric neuroendocrine carcinoma", "Gastric Neuroendocrine Carcinoma", "Gastric (Stomach) Neuroendocrine Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric neuroendocrine carcinoma", "shortest_name_length": 11}
{"curie": "UMLS:C0919956", "names": ["Lumbar Vertebral Fracture L2", "Lumbar vertebral fracture L2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lumbar vertebral fracture L2", "shortest_name_length": 28}
{"curie": "MONDO:0006749", "names": ["Spitz Nevus", "Spitz nevus", "SPITZ NEVUS", "spitz nevus", "nevus spitz", "spitz naevus", "Nevus, Spitz", "Spitz naevus", "naevus spitz", "Juvenila nevus", "Juvenile nevus", "Juvenile Nevus", "Juvenila naevus", "[M] Spitz nevus", "Juvenile naevus", "[M] Spitz naevus", "Juvenila melanoma", "Juvenile melanoma", "[M]Juvenila nevus", "juvenile melanoma", "[M]Juvenila naevus", "[M]Juvenila melanoma", "Juvenile melanoma benign", "benign juvenile melanoma", "Benign Juvenile Melanoma", "Spindle and epithelioid nevus", "Spindle and epithelioid naevus", "Epithelioid and spindle cell nevus", "epithelioid and spindle cell nevus", "Nevus, Epithelioid and Spindle Cell", "Nevus, Spindle Cell and Epithelioid", "Epithelioid and spindle cell naevus", "Pigmented spindle cell nevus of Reed", "Pigmented spindle cell naevus of Reed", "[M]Epithelioid and spindle cell nevus", "[M]Epithelioid and spindle cell naevus", "Spindle and/ or Epithelioid Cell Nevus", "Mixed Epithelioid and Spindle Cell Melanoma", "mixed epithelioid and spindle cell melanoma", "Mixed epithelioid and spindle cell melanoma", "Epithelioid and spindle cell nevus (disorder)", "epithelioid and spindle cell nevus (diagnosis)", "Epithelioid and spindle cell nevus (morphologic abnormality)", "Mixed epithelioid and spindle cell melanoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed epithelioid and spindle cell melanoma", "shortest_name_length": 11}
{"curie": "MONDO:0015459", "names": ["NPC", "NPCA", "nasopharynx cancer", "Nasopharynx Cancer", "Cancer of Nasopharynx", "Nasopharyngeal Cancer", "NASOPHARYNGEAL CANCER", "nasopharynx carcinoma", "nasopharyngeal cancer", "cancer of nasopharynx", "NASOPHARYNX, CARCINOMA", "Carcinoma of Nasopharynx", "carcinoma nasopharyngeal", "carcinoma of nasopharynx", "Nasopharyngeal Carcinoma", "Carcinoma;nasopharyngeal", "Nasopharyngeal carcinoma", "NASOPHARYNGEAL CARCINOMA", "nasopharyngeal carcinoma", "cancer of the nasopharynx", "Nasopharyngeal Carcinomas", "carcinomas nasopharyngeal", "Carcinoma, Nasopharyngeal", "Cancer of the Nasopharynx", "Carcinomas, Nasopharyngeal", "carcinoma of the nasopharynx", "nasopharyngeal throat cancer", "Nasopharyngeal Throat Cancer", "Carcinoma of the Nasopharynx", "malignant Nasopharyngeal tumor", "malignant nasopharyngeal tumor", "carcinoma of the nasopharyngeal", "NASOPHARYNGEAL CANCER, CARCINOMA", "malignant neoplasm of nasopharynx", "Nasopharyngeal carcinoma (disorder)", "carcinoma of nasopharynx (diagnosis)", "Malignant tumor of roof of nasopharynx", "Malignant tumour of roof of nasopharynx", "nasopharyngeal neoplasm wall, malignant", "malignant neoplasm of roof of nasopharynx", "Malignant neoplasm of roof of nasopharynx", "malignant neoplasm of nasopharyngeal wall", "Malignant neoplasm of nasopharyngeal wall", "Squamous cell carcinoma of the nasopharynx", "squamous cell carcinoma of the nasopharynx", "Malignant neoplasm of nasopharyngeal wall NOS", "Malignant tumor of lateral wall of nasopharynx", "malignant tumor of lateral wall of nasopharynx", "Malignant neoplasm of nasopharyngeal wall, NOS", "Malignant tumor of superior wall of nasopharynx", "Malignant tumour of lateral wall of nasopharynx", "Malignant tumor of anterior wall of nasopharynx", "malignant tumor of anterior wall of nasopharynx", "malignant tumor of superior wall of nasopharynx", "malignant tumor of posterior wall of nasopharynx", "Malignant tumour of superior wall of nasopharynx", "Malignant tumour of anterior wall of nasopharynx", "Malignant tumor of posterior wall of nasopharynx", "Malignant tumour of posterior wall of nasopharynx", "Malignant neoplasm of lateral wall of nasopharynx", "malignant neoplasm of lateral wall of nasopharynx", "malignant neoplasm of superior wall of nasopharynx", "Malignant neoplasm of anterior wall of nasopharynx", "Malignant neoplasm of superior wall of nasopharynx", "malignant neoplasm of anterior wall of nasopharynx", "Malignant neoplasm of posterior wall of nasopharynx", "malignant neoplasm of posterior wall of nasopharynx", "Malignant neoplasm of nasopharyngeal wall (disorder)", "malignant neoplasm of nasopharyngeal wall (diagnosis)", "malignant neoplasm of nasopharynx (disorder) [ambiguous]", "nasopharyngeal neoplasm anterior wall, malignant primary", "Malignant tumor of lateral wall of nasopharynx (disorder)", "malignant neoplasm of other specified sites of nasopharynx", "primary malignant nasopharyngeal neoplasm of anterior wall", "primary malignant neoplasm of anterior wall of nasopharynx", "Primary malignant neoplasm of anterior wall of nasopharynx", "Malignant tumor of anterior wall of nasopharynx (disorder)", "Malignant tumor of posterior wall of nasopharynx (disorder)", "malignant neoplasm of lateral wall of nasopharynx (diagnosis)", "Malignant neoplasm of superior wall of nasopharynx (disorder)", "malignant neoplasm of superior wall of nasopharynx (diagnosis)", "malignant neoplasm of anterior wall of nasopharynx (diagnosis)", "malignant neoplasm of posterior wall of nasopharynx (diagnosis)", "Primary malignant neoplasm of anterior wall of nasopharynx (disorder)", "primary malignant nasopharyngeal neoplasm of anterior wall (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasopharyngeal carcinoma", "shortest_name_length": 3}
{"curie": "MONDO:0012050", "names": ["MDD1", "Unipolar Depression 1", "unipolar depression 1", "UNIPOLAR DEPRESSION 1", "Major Depressive Disorder 1", "major depressive disorder 1", "MAJOR DEPRESSIVE DISORDER 1", "major depressive disorder type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "major depressive disorder 1", "shortest_name_length": 4}
{"curie": "UMLS:C5667187", "names": ["Epstein-Barr Virus-Related Lymphoproliferative Disease with Primary Immunodeficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epstein-Barr Virus-Related Lymphoproliferative Disease with Primary Immunodeficiency", "shortest_name_length": 84}
{"curie": "MONDO:0001914", "names": ["scleromalacia perforans", "SCLEROMALACIA PERFORANS", "Scleromalacia perforans", "Scleromalacia perforans (disorder)", "scleromalacia perforans (diagnosis)", "Anterior necrotising scleritis without inflammation", "Anterior necrotizing scleritis without inflammation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scleromalacia perforans", "shortest_name_length": 23}
{"curie": "MONDO:0010883", "names": ["Zori Stalker Williams syndrome", "Zori-Stalker-Williams syndrome", "Pectus excavatum, macrocephaly and dysplastic nails", "pectus excavatum, macrocephaly and dysplastic nails", "pectus excavatum-macrocephaly-dysplastic nails syndrome", "Pectus excavatum-macrocephaly-dysplastic nails syndrome", "Pectus excavatum, macrocephaly, dysplastic nails syndrome", "Pectus Excavatum, Macrocephaly, Short Stature, Dysplastic Nails", "pectus excavatum, macrocephaly, short stature, and dysplastic nails", "PECTUS EXCAVATUM, MACROCEPHALY, SHORT STATURE, AND DYSPLASTIC NAILS", "Pectus excavatum, macrocephaly, dysplastic nails syndrome (disorder)", "Familial short stature, developmental delay, pectus abnormalities, distinctive facies, and dysplastic nails", "familial short stature, developmental delay, pectus abnormalities, distinctive facies, and dysplastic nails"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pectus excavatum-macrocephaly-dysplastic nails syndrome", "shortest_name_length": 30}
{"curie": "UMLS:C1334221", "names": ["Intermediate Risk Gastric GIST", "Intermediate Risk Gastric Gastrointestinal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intermediate Risk Gastric Gastrointestinal Stromal Tumor", "shortest_name_length": 30}
{"curie": "MONDO:0007940", "names": ["Mhs3", "MHS3", "malignant hyperthermia susceptibility 3", "Malignant hyperthermia susceptibility type 3", "MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 3", "Malignant hyperpyrexia susceptibility type 3", "malignant hyperpyrexia susceptibility type 3", "malignant hyperthermia, susceptibility to, 3", "malignant hyperthermia susceptibility type 3", "malignant hyperthermia, susceptibility to, type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant hyperthermia, susceptibility to, 3", "shortest_name_length": 4}
{"curie": "MONDO:0003372", "names": ["Vulvar Leiomyosarcoma", "vulvar leiomyosarcoma", "leiomyosarcoma of vulva", "mammalian vulva leiomyosarcoma", "vulvar myosarcoma leiomyosarcoma", "leiomyosarcoma of mammalian vulva", "leiomyosarcoma of vulva (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar leiomyosarcoma", "shortest_name_length": 21}
{"curie": "UMLS:C1708187", "names": ["Gardner Fibroma", "Gardner fibroma", "Gardner's Fibroma", "Desmoid Precursor Lesion", "Gardner-Associated Fibroma", "Gardner fibroma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gardner Fibroma", "shortest_name_length": 15}
{"curie": "UMLS:C4743561", "names": ["Refractory Lung Small Cell Carcinoma", "Refractory Small Cell Lung Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Lung Small Cell Carcinoma", "shortest_name_length": 36}
{"curie": "UMLS:C0033139", "names": ["primary insomnia", "Primary Insomnia", "Primary insomnia", "primary; insomnia", "insomnia; primary", "Insomnia, Primary", "Idiopathic insomnia", "Primary insomnia (disorder)", "primary insomnia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Insomnia", "shortest_name_length": 16}
{"curie": "MONDO:0008798", "names": ["NDNC4", "Anonychia", "anonychia", "ANONYCHIA", "Claw absent", "Nail absent", "Absent nails", "Aplastic nails", "ANN - Anonychia", "anonychia totalis", "ANONYCHIA TOTALIS", "Isolated anonychia", "Anonychia congenita", "anonychia congenita", "HYPONYCHIA congenita", "Anonychia (disorder)", "Hyponychia congenita", "HYPONYCHIA CONGENITA", "anonychia (diagnosis)", "Congenital absent nails", "anonychia congenita totalis", "Anonychia congenita totalis", "Isolated congenital anonychia", "ANONYCHIA/HYPONYCHIA CONGENITA", "anonychia/hyponychia congenita", "RSPO4 isolated congenital anonychia", "Congenital absence of nails (anonychia)", "nonsyndromic congenital nail disorder 4", "nail disorder, nonsyndromic congenital, 4", "NAIL DISORDER, NONSYNDROMIC CONGENITAL, 4", "nonsyndromic congenital nail disorder type 4", "nail disorder, nonsyndromic congenital, type 4", "isolated congenital anonychia caused by mutation in RSPO4", "Complete absence of all fingernails (anonychia), congenital"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nonsyndromic congenital nail disorder 4", "shortest_name_length": 5}
{"curie": "UMLS:C2348873", "names": ["BilIN-1", "Biliary Intraepithelial Neoplasia-1", "Grade 1 Biliary Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Biliary Intraepithelial Neoplasia-1", "shortest_name_length": 7}
{"curie": "MONDO:0001041", "names": ["Dentin caries", "dentin caries", "Dentine caries", "caries; dentin", "dentin; caries", "caries of dentin", "caries of dentine", "Caries of dentine", "Dentin caries, NOS", "dentine dental caries", "Compound dental caries", "compound dental caries", "Compound dental cavity", "Dental caries, compound", "Dental cavity, compound", "dental caries of dentine", "caries of dentin (diagnosis)", "Dental caries extending into dentin", "dental caries extending into dentine", "Dental caries extending into dentine", "Dental caries confined to enamel and dentine", "Dental caries extending into dentin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dentin caries", "shortest_name_length": 13}
{"curie": "MONDO:0013873", "names": ["IMAGE", "IMAGE Syndrome", "IMAGe syndrome", "IMAGE SYNDROME", "IMAGe Syndrome", "intrauterine growth retardation - metaphyseal dysplasia - adrenal hypoplasia congenita - genital anomalies", "intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenita, genital abnormalities", "INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIA CONGENITA, AND GENITAL ANOMALIES", "intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies", "Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, And Genital Anomalies", "intrauterine growth retardation-metaphyseal dysplasia-adrenal hypoplasia congenita-genital anomalies syndrome", "Intrauterine growth retardation-metaphyseal dysplasia-adrenal hypoplasia congenita-genital anomalies syndrome", "Intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomaly syndrome", "Intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomaly syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IMAGe syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C5417719", "names": ["MTM-HCC", "Macrotrabecular Massive Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Macrotrabecular Massive Hepatocellular Carcinoma", "shortest_name_length": 7}
{"curie": "MONDO:0021726", "names": ["RCL", "abdomen cystic lymphangioma", "abdominal cystic lymphangioma", "Abdominal cystic lymphangioma", "Retroperitoneal cystic lymphangioma", "retroperitoneal cystic lymphangioma", "abdominal retroperitoneal lymphangioma", "Abdominal retroperitoneal lymphangioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "abdominal cystic lymphangioma", "shortest_name_length": 3}
{"curie": "MONDO:0001512", "names": ["Intermittent proptosis", "intermittent proptosis", "intermittent exophthalmos", "Intermittent exophthalmos", "exophthalmos; intermittent", "intermittent; exophthalmos", "intermittent bulging of eyes", "Intermittent exophthalmos (disorder)", "intermittent bulging of eyes (symptom)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intermittent proptosis", "shortest_name_length": 22}
{"curie": "UMLS:C0236701", "names": ["Cocaine induced mood disorder", "Cocaine-induced mood disorder", "cocaine-induced mood disorder", "Cocaine-induced mood disorder (disorder)", "cocaine-induced mood disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cocaine-induced mood disorder", "shortest_name_length": 29}
{"curie": "MONDO:0002719", "names": ["Conus Medullaris Tumor", "conus medullaris tumor", "Tumor of Conus Medullaris", "tumor of Conus Medullaris", "conus medullaris neoplasm", "Conus Medullaris Neoplasm", "tumor of conus medullaris", "neoplasm of conus medullaris", "Neoplasm of Conus Medullaris", "tumor of the conus medullaris", "Tumor of the Conus Medullaris", "neoplasm of the conus medullaris", "Neoplasm of the Conus Medullaris", "conus medullaris tumor (diagnosis)", "conus medullaris neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "conus medullaris neoplasm", "shortest_name_length": 22}
{"curie": "UMLS:C0205646", "names": ["Basal cell adenoma", "Basal Cell Adenoma", "basal cell; adenoma", "Basal Cell Adenomas", "adenoma; basal cell", "Adenoma, Basal Cell", "Adenomas, Basal Cell", "Salivary Gland Basal Cell Adenoma", "Basal Cell Adenoma of Salivary Gland", "basal cell adenoma of salivary gland", "Basal Cell Adenoma of the Salivary Gland", "Basal cell adenoma (morphologic abnormality)", "basal cell adenoma of salivary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenoma, Basal Cell", "shortest_name_length": 18}
{"curie": "MONDO:0060745", "names": ["IDDECA", "intellectual developmental disorder with or without epilepsy or cerebellar ataxia", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder with or without epilepsy or cerebellar ataxia", "shortest_name_length": 6}
{"curie": "OMIM:615969", "names": ["AFPD", "ALPHA-FETOPROTEIN DEFICIENCY", "alpha-Fetoprotein Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 4}
{"curie": "MONDO:0024268", "names": ["piedra", "mycosis superficial", "superficial mycosis", "Superficial mycosis", "mycosis; superficial", "superficial; mycosis", "Superficial mycosis (disorder)", "superficial mycosis (diagnosis)", "steroid-modified tinea infection", "Superficial mycosis, unspecified", "Steroid-modified tinea infection", "stratum corneum of epidermis fungal infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "superficial mycosis", "shortest_name_length": 6}
{"curie": "MONDO:0007547", "names": ["wen", "Wen", "wens", "Steatoma", "steatoma", "horn cyst", "Skin cyst", "Horn Cyst", "Horn cyst", "Horn cysts", "Keratin Cyst", "Keratin cyst", "keratin cyst", "SQUAMOUS CYST", "squamous cyst", "Sebaceous cyst", "inclusion cyst", "sebaceous cyst", "CYST EPIDERMAL", "SEBACEOUS CYST", "CYST SEBACEOUS", "Cyst sebaceous", "Cyst epidermal", "Cyst;sebaceous", "EPIDERMAL CYST", "INCLUSION CYST", "Epidermal cyst", "Sebaceous Cyst", "Inclusion Cyst", "Inclusion cyst", "Epidermal Cyst", "epidermal cyst", "epidermoid cyst", "Epidermal Cysts", "keratinous cyst", "Epidermoid cyst", "epidermal cysts", "sebaceous cysts", "cyst epithelial", "cyst; inclusion", "Keratinous cyst", "Epidermoid Cyst", "cyst; epidermal", "Cyst;epidermoid", "sebaceous; cyst", "Sebaceous Cysts", "Cyst, Sebaceous", "cyst; sebaceous", "inclusion; cyst", "Cyst, Epidermal", "epithelial cyst", "epidermal; cyst", "EPIDERMOID CYST", "cysts inclusion", "Cyst, sebaceous", "Epithelial Cyst", "Keratinous Cyst", "Epithelial cyst", "EPIDERMOID CYSTS", "epithelial; cyst", "epidermoid cysts", "Cysts, Epidermal", "cysts keratinous", "Epidermoid cysts", "Cyst, Epidermoid", "cyst; epithelial", "Epidermoid Cysts", "Cysts, Sebaceous", "cysts epithelial", "Cyst, epithelial", "Keratinising cyst", "Cysts, Epidermoid", "Infundibular cyst", "Keratinizing cyst", "keratinizing cyst", "Keratinizing Cyst", "Infundibular Cyst", "infundibular cyst", "Inclusion cyst, NOS", "Epidermal cyst, NOS", "Epithelial cyst, NOS", "Epithelium lined cyst", "Cyst, epithelium lined", "epidermoid cyst of skin", "Epidermoid cyst of skin", "Epidermal inclusion cyst", "Epidermal Inclusion Cyst", "epidermal inclusion cyst", "cysts epidermal inclusion", "Keratinizing cyst of skin", "Epithelial inclusion cyst", "Keratinising cyst of skin", "sebaceous cyst (diagnosis)", "cysts epithelial inclusion", "Epidermoid cyst (disorder)", "Cyst, epithelial inclusion", "Follicular infundibular cyst", "Keratinizing cyst (disorder)", "Follicular Infundibular Cyst", "EIC - Epidermal inclusion cyst", "Epidermoid cyst of skin (disorder)", "epidermoid cyst of skin (diagnosis)", "epidermal inclusion cyst (diagnosis)", "Keratinizing cyst of skin (disorder)", "Sebaceous cyst (morphologic abnormality)", "Epidermoid cyst (morphologic abnormality)", "Keratinizing cyst (morphologic abnormality)", "Epidermal inclusion cyst (morphologic abnormality)", "Epithelial inclusion cyst (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermoid cysts", "shortest_name_length": 3}
{"curie": "UMLS:C5419170", "names": ["Non-Neoplastic Trigeminal Nerve Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Trigeminal Nerve Disorder", "shortest_name_length": 40}
{"curie": "MONDO:0033640", "names": ["VDDR3", "VITAMIN D-DEPENDENT RICKETS, TYPE 3", "vitamin D-dependent rickets, type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitamin D-dependent rickets, type 3", "shortest_name_length": 5}
{"curie": "MONDO:0008258", "names": ["platelet signal processing defect", "Platelet Signal Processing Defect", "PLATELET SIGNAL PROCESSING DEFECT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "platelet signal processing defect", "shortest_name_length": 33}
{"curie": "MONDO:0018121", "names": ["mtDNA maintenance syndrome", "mitochondrial DNA maintenance syndrome", "inborn error of mitochondrial genome maintenance", "inborn mitochondrial genome maintenance disorder", "rare inborn error of mitochondrial genome maintenance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial DNA maintenance syndrome", "shortest_name_length": 26}
{"curie": "UMLS:C4683434", "names": ["Thyroid Gland Anaplastic Carcinoma by AJCC v8 Stage", "Thyroid Gland Undifferentiated (Anaplastic) Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Anaplastic Carcinoma by AJCC v8 Stage", "shortest_name_length": 51}
{"curie": "UMLS:C0151626", "names": ["epidermal necrolysis", "Necrolysis epidermal", "EPIDERMAL NECROLYSIS", "NECROLYSIS EPIDERMAL", "Epidermal necrolysis", "necrolysis epidermal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epidermal necrolysis", "shortest_name_length": 20}
{"curie": "UMLS:C0156384", "names": ["vagina dysplasia", "VAGINAL DYSPLASIA", "vaginal dysplasia", "vagina; dysplasia", "dysplasia; vagina", "Vaginal dysplasia", "dysplasia of vagina", "Dysplasia of vagina", "vaginal dysplasia (diagnosis)", "Dysplasia of vagina (disorder)", "Dysplasia of vagina, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dysplasia of vagina", "shortest_name_length": 16}
{"curie": "UMLS:C0852958", "names": ["jugular; thrombosis", "thrombosis; jugular", "Jugular vein thrombosis", "Thrombosis of jugular vein", "Thrombosis of jugular vein (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thrombosis of jugular vein", "shortest_name_length": 19}
{"curie": "MONDO:0024340", "names": ["retina neuroblastoma", "retinal neuroblastoma", "Retinal Neuroblastoma", "Neuroblastoma of Retina", "neuroblastoma of retina", "Neuroblastoma of the Retina", "neuroblastoma of the retina"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal neuroblastoma", "shortest_name_length": 20}
{"curie": "MONDO:0018663", "names": ["PHASK", "SKPHA", "REGRESSIVE SPONDYLOMETAPHYSEAL DYSPLASIA", "Regressive spondylometaphyseal dysplasia", "regressive spondylometaphyseal dysplasia", "PELGER-HUET ANOMALY WITH MILD SKELETAL ANOMALIES", "Pelger-Huet anomaly with mild skeletal anomalies", "Regressive spondylometaphyseal dysplasia (disorder)", "RHIZOMELIC SKELETAL DYSPLASIA WITH OR WITHOUT PELGER-HUET ANOMALY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "regressive spondylometaphyseal dysplasia", "shortest_name_length": 5}
{"curie": "MONDO:0021390", "names": ["Ureter Polyp", "Ureter polyp", "ureter polyp", "ureter; polyp", "polyps ureter", "polyp; ureter", "Ureteral Polyp", "Ureteric polyp", "ureteral polyp", "Ureteral polyp", "Polyp of Ureter", "Polyp of ureter", "polyp of ureter", "Ureteral polyps", "Polyp of the ureter", "Polyp of the Ureter", "polyp of the ureter", "Ureteric polyp (disorder)", "ureteral polyp (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyp of ureter", "shortest_name_length": 12}
{"curie": "UMLS:C5236090", "names": ["Locally Advanced Unresectable Malignant PEComa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Unresectable Malignant PEComa", "shortest_name_length": 46}
{"curie": "UMLS:C4725810", "names": ["Refractory Malignant Male Reproductive System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Malignant Male Reproductive System Neoplasm", "shortest_name_length": 54}
{"curie": "UMLS:C5669770", "names": ["Diffuse Low Grade Glioma, FGFR1 TKD-Duplicated", "Diffuse Low-Grade Glioma, FGFR1 TKD-Duplicated", "Diffuse Low-Grade Glioma, FGFR1 Tyrosine Kinase Domain-Duplicated", "Diffuse Low Grade Glioma, FGFR1 Tyrosine Kinase Domain-Duplicated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse Low Grade Glioma, FGFR1 Tyrosine Kinase Domain-Duplicated", "shortest_name_length": 46}
{"curie": "UMLS:C1333468", "names": ["Esophageal Squamous Dysplasia", "Esophageal Squamous Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Squamous Intraepithelial Neoplasia", "shortest_name_length": 29}
{"curie": "UMLS:C1335425", "names": ["Plasma Cell Myeloma PTLD", "Plasma Cell Myeloma Post-Transplant Lymphoproliferative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Plasma Cell Myeloma Post-Transplant Lymphoproliferative Disorder", "shortest_name_length": 24}
{"curie": "UMLS:C3714043", "names": ["Trisomy Xq28", "Chromosome Xq28 trisomy", "Chromosome Xq28 trisomy syndrome", "Chromosome Xq28 trisomy (disorder)", "Chromosome Xq28 trisomy syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Trisomy Xq28", "shortest_name_length": 12}
{"curie": "UMLS:C0549350", "names": ["CONJUNCTIVITIS AGGRAVATED", "Conjunctivitis aggravated", "Conjunctivitis exacerbated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conjunctivitis aggravated", "shortest_name_length": 25}
{"curie": "MONDO:0020797", "names": ["bend", "choke", "Bends", "BENDS", "bends", "CHOKES", "chokes", "bending", "choking", "the bends", "The bends", "CAISSON DIS", "AEROBULLOSIS", "aerobullosis", "DIVER DISEASE", "divers' palsy", "Divers' palsy", "disease divers", "caisson disease", "Caisson Disease", "CAISSON DISEASE", "Caisson disease", "Bends (disorder)", "caisson; disease", "Caisson Diseases", "caissons disease", "Disease, Caisson", "divers' paralysis", "Nitrogen narcosis", "nitrogen narcosis", "Diseases, Caisson", "Nitrogen Narcosis", "Nitrogen Narcoses", "Divers' paralysis", "Narcoses, Nitrogen", "diver's; paralysis", "Narcosis, Nitrogen", "Compressed-air disease", "compressed air disease", "compressed-air disease", "DECOMPRESSION SICKNESS", "decompression; disease", "Decompression sickness", "decompression sickness", "Decompression Sickness", "Compressed air disease", "Sickness, Decompression", "Divers' palsy or paralysis", "Diver's palsy or paralysis", "Rapture of the deep syndrome", "Nitrogen narcosis (disorder)", "compression; diver's squeeze", "diver's squeeze; compression", "disease (or disorder); caisson", "decompression sickness (diagnosis)", "diver's palsy, paralysis or squeeze", "disease (or disorder); decompression", "disease (or disorder); compressed air", "Caisson disease [decompression sickness]", "Effects of caisson disease [decompression sickness]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "decompression sickness", "shortest_name_length": 4}
{"curie": "MONDO:0006046", "names": ["serous cystadenoma", "Serous cystadenocarcinoma ovary", "serous cystadenocarcinoma ovary", "cystadenocarcinoma ovary serous", "ovarian serous cystadenocarcinoma", "Serous ovarian cystadenocarcinoma", "Ovarian Serous Cystadenocarcinoma", "cystadenocarcinoma ovarian serous", "serous cystadenocarcinoma of ovary", "serous cystadenocarcinoma of the ovary", "ovary cancer, serous cystadenocarcinoma", "cystadenocarcinoma of the ovary, serous", "ovarian cancer, serous cystadenocarcinoma", "serous cystadenocarcinoma of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian serous cystadenocarcinoma", "shortest_name_length": 18}
{"curie": "UMLS:C2987498", "names": ["Stage I Vulvar Cancer", "Stage I Vulvar Carcinoma", "Stage I Vulvar Cancer AJCC v7", "Stage I Vulvar Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Vulvar Cancer", "shortest_name_length": 21}
{"curie": "MONDO:0013252", "names": ["WABS", "WARSAW breakage syndrome", "Warsaw breakage syndrome", "WARSAW BREAKAGE SYNDROME", "Warsaw Breakage Syndrome", "Warsaw breakage syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Warsaw breakage syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C1332568", "names": ["Blastoid Follicular Lymphoma", "Diffuse Blastoid B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse Blastoid B-Cell Lymphoma", "shortest_name_length": 28}
{"curie": "UMLS:C0876998", "names": ["heart; thrombosis", "thrombosis; heart", "Cardiac thrombosis", "cardiac thrombosis", "thrombosis cardiac", "Intracardiac thrombus", "intracardiac thrombus", "Intracardiac thrombosis", "intracardiac thrombosis", "intracardiac; thrombosis", "thrombosis; intracardiac", "Thrombus of cardiac chamber", "Thrombus of chamber of heart", "intracardiac thrombosis (diagnosis)", "Thrombus of chamber of heart (disorder)", "complications heart disease intracardiac thrombosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thrombus of cardiac chamber", "shortest_name_length": 17}
{"curie": "MONDO:0020774", "names": ["Menke-Hennekam syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Menke-Hennekam syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0020308", "names": ["late-onset benign childhood occipital epilepsy", "benign childhood occipital epilepsy, Gastaut type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign childhood occipital epilepsy, Gastaut type", "shortest_name_length": 46}
{"curie": "MONDO:0005290", "names": ["rhabdomyolysis", "RHABDOMYOLYSIS", "Rhabdomyolysis", "Rhabdomyolyses", "Skeletal muscle necrosis", "rhabdomyolysis (disease)", "Rhabdomyolysis (disorder)", "rhabdomyolysis (diagnosis)", "Necrosis of skeletal muscle", "Breakdown of skeletal muscle", "Necrosis of skeletal muscle (finding)", "Rhabdomyolysis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rhabdomyolysis", "shortest_name_length": 14}
{"curie": "MONDO:0012492", "names": ["RLS3", "restless legs syndrome 3", "restless legs syndrome, susceptibility to, 3", "RESTLESS LEGS SYNDROME, SUSCEPTIBILITY TO, 3", "RESTLESS LEGS SYNDROME, SUSCEPTIBILITY TO, 3 (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "restless legs syndrome, susceptibility to, 3", "shortest_name_length": 4}
{"curie": "UMLS:C5206820", "names": ["Localized Breast Carcinoma", "Non-Metastatic Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized Breast Carcinoma", "shortest_name_length": 26}
{"curie": "UMLS:C4764209", "names": ["Refractory Endometrial Carcinosarcoma", "Refractory Uterine Corpus Carcinosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Uterine Corpus Carcinosarcoma", "shortest_name_length": 37}
{"curie": "UMLS:C5447976", "names": ["Metastatic Medulloblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Medulloblastoma", "shortest_name_length": 26}
{"curie": "UMLS:C5669687", "names": ["Metastatic Hilar Cholangiocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Hilar Cholangiocarcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C0149532", "names": ["FB Esophagus", "FB Oesophagus", "foreign body; esophagus", "Esophageal foreign body", "esophageal foreign body", "ESOPHAGUS, FOREIGN BODY", "bodies esophagus foreign", "Foreign Body in Esophagus", "Foreign body in esophagus", "bodies esophageal foreign", "foreign body of esophagus", "foreign body in esophagus", "foreign body in oesophagus", "Foreign body in oesophagus", "Foreign body (in);oesophagus", "foreign body in the esophagus", "Esophageal foreign body (diagnosis)", "Foreign body in esophagus (disorder)", "foreign body of esophagus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Foreign body in esophagus", "shortest_name_length": 12}
{"curie": "MONDO:0009957", "names": ["Reese Retinal Dysplasia", "Reese retinal dysplasia", "REESE RETINAL DYSPLASIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reese retinal dysplasia", "shortest_name_length": 23}
{"curie": "UMLS:C0153289", "names": ["echinococcus granulosus of liver", "Echinococcus granulosus infection of liver", "echinococcus granulosus of liver (diagnosis)", "Echinococcus granulosus infection of liver (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Echinococcus granulosus infection of liver", "shortest_name_length": 32}
{"curie": "UMLS:C4744367", "names": ["Sellar Neuroblastoma", "Sellar Esthesioneuroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sellar Neuroblastoma", "shortest_name_length": 20}
{"curie": "MONDO:0100109", "names": ["Zinner syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Zinner syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0003768", "names": ["signet ring mucinous carcinoma", "Cervical Mucinous Adenocarcinoma, Signet Ring Cell Type", "Cervical Mucinous Adenocarcinoma, Signet Ring Cell-Type", "cervical mucinous adenocarcinoma, signet Ring cell type", "Cervical Mucinous Adenocarcinoma, Signet-Ring Cell Type", "signet ring cell variant cervical mucinous adenocarcinoma", "Cervical Mucinous Adenocarcinoma, Signet Ring Cell Variant", "cervical mucinous adenocarcinoma, signet Ring cell variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "signet ring cell variant cervical mucinous adenocarcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0021607", "names": ["eyelid basal cell papilloma", "eyelid seborrheic keratosis", "Eyelid seborrheic keratosis", "Eyelid Basal Cell Papilloma", "Eyelid Seborrheic Keratosis", "Eyelid seborrhoeic keratosis", "Basal cell papilloma of eyelid", "Seborrheic keratosis of eyelid", "Seborrheic Keratosis of Eyelid", "basal cell papilloma of eyelid", "Basal Cell Papilloma of Eyelid", "seborrheic keratosis of eyelid", "Seborrhoeic keratosis of eyelid", "Basal Cell Papilloma of the Eyelid", "Seborrheic Keratosis of the Eyelid", "basal cell papilloma of the eyelid", "seborrheic keratosis of the eyelid", "Seborrheic keratosis of eyelid (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eyelid seborrheic keratosis", "shortest_name_length": 27}
{"curie": "UMLS:C0271932", "names": ["chronic renal failure anemia", "Chronic renal failure anemia", "anemia chronic renal failure", "anemia chronic failure renal", "Chronic renal failure anaemia", "anemia of chronic renal failure", "Anemia of chronic renal failure", "Anaemia of chronic renal failure", "Anemia of chronic renal insufficiency", "Anaemia of chronic renal insufficiency", "Anemia secondary to chronic renal failure", "Anaemia secondary to chronic renal failure", "Anemia of chronic renal failure (disorder)", "anemia of chronic renal failure (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anemia of chronic renal failure", "shortest_name_length": 28}
{"curie": "MONDO:0100342", "names": ["glioma", "Malignant Glioma", "glial cell tumor", "Neuroglial tumor", "Malignant glioma", "malignant glioma", "neuroglial tumor", "High Grade Glioma", "high-grade glioma", "Glioma, malignant", "GLIOMA, MALIGNANT", "high grade glioma", "malignant gliomas", "High-Grade Glioma", "Glioma, Malignant", "Malignant Gliomas", "glioma, malignant", "Gliomas, Malignant", "malignant glial tumor", "Malignant Glial Tumor", "Glial tumors malignant", "Glial tumours malignant", "Malignant Glial Neoplasm", "malignant glial neoplasm", "malignant Neuroglial tumor", "Malignant Neuroglial Tumor", "malignant neuroglial tumor", "malignant neuroglial neoplasm", "Malignant Neuroglial Neoplasm", "Glioma, malignant (morphologic abnormality)", "Glioma, NOS (except Nasal glioma, not neoplastic)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant glioma", "shortest_name_length": 6}
{"curie": "MONDO:0014869", "names": ["HLASA", "hydrops, lactic acidosis, and sideroblastic anemia", "HYDROPS, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA", "hydrops-lactic acidosis-sideroblastic anemia-multisystemic failure syndrome", "Hydrops-lactic acidosis-sideroblastic anemia-multisystemic failure syndrome", "Hydrops, lactic acidosis, sideroblastic anemia, multisystemic failure syndrome", "Hydrops, lactic acidosis, sideroblastic anaemia, multisystemic failure syndrome", "Hydrops, lactic acidosis, sideroblastic anemia, multisystemic failure syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hydrops-lactic acidosis-sideroblastic anemia-multisystemic failure syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0013722", "names": ["HLD8", "4H Syndrome", "4H LEUKODYSTROPHY 2", "POLR3B leukodystrophy", "hypomyelinating leukodystrophy 8", "Hypomyelinating Leukodystrophy-8", "leukodystrophy caused by mutation in POLR3B", "cerebellar hypoplasia with endosteal sclerosis", "Cerebellar hypoplasia with endosteal sclerosis", "CEREBELLAR HYPOPLASIA WITH ENDOSTEAL SCLEROSIS", "endosteal sclerosis-cerebellar hypoplasia syndrome", "Endosteal sclerosis-cerebellar hypoplasia syndrome", "Hypomyelination-Hypogonadotropic Hypogonadism-Hypodontia Syndrome", "hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism", "LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/OR HYPOGONADOTROPIC HYPOGONADISM", "leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism", "shortest_name_length": 4}
{"curie": "MONDO:0011948", "names": ["PCH3", "clam", "CLAM", "PCH without dyskinesia", "Pch With Optic Atrophy", "PCH with optic atrophy", "PCH WITH OPTIC ATROPHY", "Pch with optic atrophy", "Pontocerebellar Hypoplasia Type 3", "Pontocerebellar hypoplasia type 3", "pontocerebellar hypoplasia type 3", "PONTOCEREBELLAR HYPOPLASIA, TYPE 3", "pontocerebellar hypoplasia, type 3", "PCH3 - pontocerebellar hypoplasia type 3", "Congenital pontocerebellar hypoplasia type 3", "PCLO non-syndromic pontocerebellar hypoplasia", "Cerebellar Atrophy With Progressive Microcephaly", "CEREBELLAR ATROPHY WITH PROGRESSIVE MICROCEPHALY", "Cerebellar atrophy with progressive microcephaly", "cerebellar atrophy with progressive microcephaly", "Congenital pontocerebellar hypoplasia type 3 (disorder)", "non-syndromic pontocerebellar hypoplasia caused by mutation in PCLO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pontocerebellar hypoplasia type 3", "shortest_name_length": 4}
{"curie": "MONDO:0007770", "names": ["HYPERPIGMENTATION OF FULDAUER AND KUIJPERS", "hyperpigmentation of Fuldauer and Kuijpers", "Hyperpigmentation of Fuldauer and Kuijpers"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperpigmentation of Fuldauer and Kuijpers", "shortest_name_length": 42}
{"curie": "MONDO:0001633", "names": ["RETINAL ARTERY CENTRAL OCCLUSION", "central retinal artery occlusion", "Central retinal artery occlusion", "Central Retinal Artery Occlusion", "occlusion; artery, retina, central", "central retinal arterial occlusion", "Central Retinal Arterial Occlusion", "occlusion of central retinal artery", "obstruction; artery, retina, central", "CRA - Central retinal artery occlusion", "CRAO - Central retinal artery occlusion", "retina; occlusion central retinal artery", "occlusion; retina, central retinal artery", "Central retinal artery occlusion (disorder)", "occlusion of central retinal artery (diagnosis)", "central retinal artery occlusion (physical finding)", "artery; occlusion, artery, retinal, central retinal artery"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central retinal artery occlusion", "shortest_name_length": 32}
{"curie": "UMLS:C1333993", "names": ["Familial Paraganglioma", "familial paraganglioma", "Hereditary Paraganglioma", "hereditary paraganglioma", "paraganglioma, hereditary", "SDH-Related Familial Paraganglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Familial Paraganglioma", "shortest_name_length": 22}
{"curie": "MONDO:0006524", "names": ["Herxheimer disease", "Dermatitis atrophicans", "primary diffuse atrophy", "Dermatitis chronica atrophicans", "Acrodermatitis chronica atrophicans", "acrodermatitis chronica atrophicans", "Acrodermatitis atrophicans chronica", "Acrodermatitis atrophicans chronica (disorder)", "acrodermatitis chronica atrophicans (diagnosis)", "Other specified hypertrophic and atrophic conditions of skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acrodermatitis chronica atrophicans", "shortest_name_length": 18}
{"curie": "UMLS:C1708879", "names": ["Malignant Germinative Follicular Epithelium Tumor", "Malignant Germinative Follicular Epithelium Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Germinative Follicular Epithelium Neoplasm", "shortest_name_length": 49}
{"curie": "MONDO:0021166", "names": ["Inflammatory Disease", "inflammatory disease", "Inflammatory_Disease", "disease inflammatory", "Inflammatory disease", "inflammatory disorder", "diseases inflammatory", "Inflammatory Disorder", "Inflammatory disorder", "disorders inflammatory", "Inflammatory disorder (disorder)", "anatomical structure inflammation", "inflammatory disorder (diagnosis)", "inflammation of anatomical structure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory disease", "shortest_name_length": 20}
{"curie": "UMLS:C0853057", "names": ["Ductus arteriosus stenosis fetal", "Ductus arteriosus stenosis foetal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ductus arteriosus stenosis fetal", "shortest_name_length": 32}
{"curie": "MONDO:0001806", "names": ["Vaginal Squamous Tumor", "vaginal squamous tumor", "vaginal squamous neoplasm", "Vaginal Squamous Neoplasm", "vagina squamous cell neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vaginal squamous tumor", "shortest_name_length": 22}
{"curie": "MONDO:0014179", "names": ["MSP3", "IBMPFD3", "multisystem Proteinopathy 3", "multisystem proteinopathy 3", "MULTISYSTEM PROTEINOPATHY 3", "HNRNPA1 inclusion body myopathy with Paget disease of bone and frontotemporal dementia", "inclusion body myopathy with early-onset paget disease without frontotemporal dementia 3", "inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 3", "INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 3", "inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia type 3", "inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 3", "inclusion body myopathy with Paget disease of bone and frontotemporal dementia caused by mutation in HNRNPA1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 3", "shortest_name_length": 4}
{"curie": "UMLS:C4553693", "names": ["IV", "Stage IV Cervical Cancer", "Stage IV Cervical Cancer AJCC v8", "Stage IV Cervical Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Cervical Cancer AJCC v8", "shortest_name_length": 2}
{"curie": "MONDO:0016723", "names": ["Pinealoma", "pineocytoma", "Pineocytoma", "Pineocytomas", "pineocytomas", "pinealocytoma", "Pinealocytoma", "Pinealocytomas", "Benign Pinealoma", "Benign pinealoma", "benign pinealoma", "pineocytoma, benign", "PINEOCYTOMA, BENIGN", "pineocytoma (disease)", "Pineocytoma (disorder)", "pineocytoma (diagnosis)", "Pineocytoma (WHO grade I)", "Pineocytoma (WHO Grade 1)", "Pineocytoma (WHO Grade I)", "Pineocytoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pineocytoma", "shortest_name_length": 9}
{"curie": "UMLS:C2981715", "names": ["stage IB mycosis fungoides/Sezary syndrome", "Stage IB Mycosis Fungoides and Sezary Syndrome", "Stage IB Mycosis Fungoides and Sézary Syndrome", "Stage IB Mycosis Fungoides and Sézary Syndrome AJCC v7", "stage IB mycosis fungoides and Sezary syndrome AJCC v7", "Stage IB Mycosis Fungoides and Sezary Syndrome AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Mycosis Fungoides and Sezary Syndrome AJCC v7", "shortest_name_length": 42}
{"curie": "MONDO:0003900", "names": ["CONNECTIVE TISSUE DISEASE", "connective tissue disease", "Connective tissue disease", "Disease;connective tissue", "Connective Tissue Disease", "Connective Tissue Disorder", "Connective Tissue Diseases", "disease, connective tissue", "Connective tissue disorder", "connective tissue disorder", "Disease, Connective Tissue", "connective tissue diseases", "tissue disease, connective", "Connective Tissue Disorders", "Connective tissue disorders", "Diseases, Connective Tissue", "connective tissue disorders", "disease of connective tissue", "Connective tissues--Diseases", "disorder of connective tissue", "Disorder of Connective Tissue", "Disorder of connective tissue", "disorders of connective tissue", "Connective tissue disorder NOS", "Connective tissue disorders NEC", "DISEASES OF THE CONNECTIVE TISSUES", "connective tissue disorder diagnosis", "Primary Disorder of Connective Tissue", "Connective tissue disease or syndrome", "connective tissue disease or disorder", "primary disorder of connective tissue", "disease or disorder of connective tissue", "Disorder of connective tissue (disorder)", "disorders of connective tissue (diagnosis)", "Diseases and Syndromes of Connective Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "connective tissue disorder", "shortest_name_length": 25}
{"curie": "UMLS:C0751666", "names": ["Type II Canavan Disease", "Canavan Disease, Type II", "Infantile Canavan Disease", "Canavan Disease, Infantile"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Canavan Disease, Infantile", "shortest_name_length": 23}
{"curie": "MONDO:0012223", "names": ["MARIE UNNA-LIKE SCALP HYPOTRICHOSIS", "Marie Unna-Like Scalp Hypotrichosis", "Marie Unna-like scalp hypotrichosis", "HYPOTRICHOSIS, PROGRESSIVE PATTERNED SCALP, WITH WIRY HAIR, ONYCHOLYSIS, AND CLEFT LIP/PALATE", "hypotrichosis, progressive patterned scalp, with wiry hair, onycholysis, and cleft lip/palate", "Hypotrichosis, Progressive Patterned Scalp, with Wiry Hair, Onycholysis, and Cleft Lip-Palate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotrichosis, progressive patterned scalp, with wiry hair, onycholysis, and cleft lip/palate", "shortest_name_length": 35}
{"curie": "MONDO:0010756", "names": ["Von Willebrand disease, X-linked", "VON WILLEBRAND DISEASE, X-LINKED FORM", "Von Willebrand Disease, X-Linked Form", "Von Willebrand disease, X-linked form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Von Willebrand disease, X-linked form", "shortest_name_length": 32}
{"curie": "UMLS:C0273487", "names": ["First-Nerve Trauma", "First Nerve Trauma", "First-Nerve Traumas", "Trauma, First-Nerve", "Traumas, First-Nerve", "n.olfactorius; injury", "Olfactory nerve injury", "olfactory nerve injury", "Cranial Nerve I Injury", "Olfactory Nerve Injury", "Olfactory Nerve Trauma", "Nerve Injury, Olfactory", "Olfactory Nerve Traumas", "Nerve Trauma, Olfactory", "Injury, Cranial Nerve I", "injury; olfactory nerve", "Trauma, Olfactory Nerve", "Injury, Olfactory Nerve", "Nerve Traumas, Olfactory", "Olfactory Nerve Injuries", "Traumas, Olfactory Nerve", "Injuries, Olfactory Nerve", "Injury to olfactory nerve", "Injury of olfactory nerve", "Nerve Injuries, Olfactory", "First cranial nerve injury", "First Cranial Nerve Injury", "Injury to 1st cranial nerve", "Traumatic First Nerve Palsy", "Traumatic First-Nerve Palsy", "Injury, First Cranial Nerve", "First-Nerve Palsy, Traumatic", "Palsy, Traumatic First-Nerve", "First Nerve Palsy, Traumatic", "Olfactory (1st) nerve injury", "First Cranial Nerve Injuries", "Injury of first cranial nerve", "Traumatic First-Nerve Palsies", "Traumatic Olfactory Neuropathy", "Palsies, Traumatic First-Nerve", "First-Nerve Palsies, Traumatic", "Olfactory Neuropathy, Traumatic", "Neuropathy, Traumatic Olfactory", "Injury of olfactory [1st ] nerve", "traumatic olfactory nerve injury", "Traumatic Olfactory Neuropathies", "Neuropathies, Traumatic Olfactory", "Olfactory Neuropathies, Traumatic", "olfactory nerve injury (diagnosis)", "Injury of olfactory nerve (disorder)", "traumatic olfactory nerve injury (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Olfactory Nerve Injuries", "shortest_name_length": 18}
{"curie": "MONDO:0012020", "names": ["Dup(22)(q11)", "dup(22)(q11)", "trisomy 22q11.2", "Trisomy 22q11.2", "22q11.2 duplication", "22q11.2 Duplication", "duplication 22q11.2", "Duplication 22q11.2", "22q11 duplication syndrome", "22q11.2 duplication syndrome", "22q11.2 microduplication syndrome", "chromosome 22q11.2 DUPLICATION syndrome", "chromosome 22q11.2 duplication syndrome", "22q11.2 duplication syndrome (disorder)", "Chromosome 22q11.2 Duplication Syndrome", "Chromosome 22q11.2 duplication syndrome", "CHROMOSOME 22q11.2 DUPLICATION SYNDROME", "22q11.2 duplication syndrome (diagnosis)", "CHROMOSOME 22q11.2 MICRODUPLICATION SYNDROME", "chromosome 22q11.2 microduplication syndrome", "Chromosome 22q11.2 microduplication syndrome", "Chromosome 22q11.2 Microduplication Syndrome", "chromosome 22q11.2 microduplication syndrome, isolated cases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 22q11.2 microduplication syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0014600", "names": ["DKCB6", "PARN dyskeratosis congenita", "autosomal recessive dyskeratosis congenita 6", "dyskeratosis congenita, autosomal recessive 6", "Dyskeratosis Congenita, Autosomal Recessive 6", "DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 6", "dyskeratosis congenita caused by mutation in PARN", "dyskeratosis congenita, autosomal recessive type 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyskeratosis congenita, autosomal recessive 6", "shortest_name_length": 5}
{"curie": "MONDO:0100379", "names": ["AML, t(1;11)(q21;q23)", "acute myeloid leukemia, t(1;11)(q21;q23)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, t(1;11)(q21;q23)", "shortest_name_length": 21}
{"curie": "MONDO:0005007", "names": ["colloid colon adenocarcinoma", "Colon Colloid Adenocarcinoma", "Colloid Colon Adenocarcinoma", "colon colloid adenocarcinoma", "Mucinous Colon Adenocarcinoma", "colon mucinous adenocarcinoma", "Colon Mucinous Adenocarcinoma", "mucinous colon adenocarcinoma", "colonic colloid adenocarcinoma", "Colon Colloidal Adenocarcinoma", "colon colloidal adenocarcinoma", "Colloidal Colon Adenocarcinoma", "colloidal colon adenocarcinoma", "Colonic Colloid Adenocarcinoma", "Colonic mucinous adenocarcinoma", "colloid adenocarcinoma of colon", "Colloid Adenocarcinoma of Colon", "colonic mucinous adenocarcinoma", "Colonic Mucinous Adenocarcinoma", "Colonic Colloidal Adenocarcinoma", "mucinous adenocarcinoma of colon", "Mucinous adenocarcinoma of colon", "colonic colloidal adenocarcinoma", "Mucinous Adenocarcinoma of Colon", "Colloidal Adenocarcinoma of Colon", "colloidal adenocarcinoma of colon", "Colloid Adenocarcinoma of the Colon", "colloid adenocarcinoma of the colon", "adenocarcinoma of the colon, colloid", "mucinous adenocarcinoma of the colon", "Mucinous Adenocarcinoma of the Colon", "Colloidal Adenocarcinoma of the Colon", "colon, mucinous adenocarcinoma of the", "colloidal adenocarcinoma of the colon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colon mucinous adenocarcinoma", "shortest_name_length": 28}
{"curie": "UMLS:C1392435", "names": ["Chiromegaly", "Cheiromegaly", "cheiromegaly", "Cheiromegaly (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cheiromegaly", "shortest_name_length": 11}
{"curie": "UMLS:C4055438", "names": ["Ascending Testicle"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ascending Testicle", "shortest_name_length": 18}
{"curie": "MONDO:0000974", "names": ["axilla lipoma", "axillary lipoma", "Axillary Lipoma", "AXILLARY LIPOMA", "Lipoma of axilla", "lipoma of axilla", "Lipoma of Axilla", "Lipoma of axilla (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "axillary lipoma", "shortest_name_length": 13}
{"curie": "MONDO:0016312", "names": ["5-fluorouracil poisoning", "5-fluorouracil intoxication", "5 alpha Fluorouracil toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "5-fluorouracil poisoning", "shortest_name_length": 24}
{"curie": "UMLS:C0234472", "names": ["Functional Aphasia", "Functional aphasia", "Aphasia, Functional", "Aphasia, functional", "Functional Aphasias", "Functional aphasia (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aphasia, Functional", "shortest_name_length": 18}
{"curie": "UMLS:C0333866", "names": ["Mild cytologic atypia", "Mild Cytologic Atypia", "Mild cytologic atypia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mild cytologic atypia", "shortest_name_length": 21}
{"curie": "UMLS:C4744834", "names": ["Recurrent Primary Peritoneal Low Grade Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Primary Peritoneal Low Grade Serous Adenocarcinoma", "shortest_name_length": 60}
{"curie": "MONDO:0010361", "names": ["MRX30", "MRX47", "XLID30", "X-linked mental retardation 47", "X-linked mental retardation 30", "mental retardation, X-linked 30", "MENTAL RETARDATION, X-LINKED 30", "mental retardation, X-linked 47", "Mental Retardation, X-Linked 30", "Mental Retardation, X-Linked 47", "MENTAL RETARDATION, X-LINKED 47", "X-linked mental retardation 30/47", "intellectual disability, X-linked 47", "mental retardation, X-linked type 30", "intellectual disability, X-linked 30", "intellectual disability, X-linked type 30", "X-linked mental retardation (MRX 47, XLMR 47)", "X-linked mental retardation 30 (MRX30, XLMR30)", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 47", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 30", "non-syndromic X-linked intellectual disability 30", "PAK3 non-syndromic X-linked intellectual disability", "intellectual developmental disorder, X-linked 30, X-linked recessive", "non-syndromic X-linked intellectual disability caused by mutation in PAK3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 30", "shortest_name_length": 5}
{"curie": "MONDO:0016480", "names": ["silver-Russell syndrome due to an imprinting defect of 11p15", "Silver-Russell syndrome due to an imprinting defect of type 11p15"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "silver-Russell syndrome due to an imprinting defect of 11p15", "shortest_name_length": 60}
{"curie": "UMLS:C4329641", "names": ["Central Nervous System Malignant Fibrous Histiocytoma", "Central Nervous System Undifferentiated Pleomorphic Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Undifferentiated Pleomorphic Sarcoma", "shortest_name_length": 53}
{"curie": "EFO:1001017", "names": ["limited scleroderma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "limited scleroderma", "shortest_name_length": 19}
{"curie": "MONDO:0010945", "names": ["RP17", "RP 17", "retinitis pigmentosa 17", "Retinitis Pigmentosa 17", "RETINITIS PIGMENTOSA 17", "CA4 retinitis pigmentosa", "retinitis pigmentosa type 17", "retinitis pigmentosa caused by mutation in CA4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 17", "shortest_name_length": 4}
{"curie": "MONDO:0013418", "names": ["AAT7", "aortic aneurysm, familial thoracic 7", "AORTIC ANEURYSM, FAMILIAL THORACIC 7", "aortic aneurysm, familial thoracic type 7", "AORTIC DISSECTION, FAMILIAL, WITH OR WITHOUT AORTIC ANEURYSM", "aortic dissection, familial, with or without aortic aneurysm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic aneurysm, familial thoracic 7", "shortest_name_length": 4}
{"curie": "MONDO:0009623", "names": ["BBS", "NBS", "NBs", "AT V1", "AT-V1", "AT-V2", "At-V1", "Seemanova syndrome", "Seemanova Syndrome", "Seemanova Syndrome 2", "Seemanova syndrome 2", "Seemanova Syndrome II", "Seemanova syndrome II", "SEEMANOVA SYNDROME II", "BERLIN BREAKAGE SYNDROME", "Berlin Breakage Syndrome", "Berlin breakage syndrome", "Syndrome, Berlin Breakage", "Seemanova syndrome type 2", "Breakage Syndrome, Berlin", "Nijmegen Breakage Syndrome", "NIJMEGEN BREAKAGE SYNDROME", "Nijmegen breakage syndrome", "Syndrome, Nijmegen Breakage", "Breakage Syndrome, Nijmegen", "ataxia-telangiectasia variant", "Ataxia-Telangiectasia Variant 1", "Ataxia Telangiectasia Variant 1", "ATAXIA-TELANGIECTASIA VARIANT V1", "Ataxia-Telangiectasia Variant V1", "ataxia-telangiectasia, variant 1", "ATAXIA-TELANGIECTASIA VARIANT V2", "Nijmegen breakage syndrome (NBS)", "Ataxia-telangiectasia, variant 1", "Ataxia-Telangiectasia Variant 1s", "ataxia-telangiectasia variant V2", "Ataxia-Telangiectasia Variant V2", "ataxia-telangiectasia variant V1", "NBS - Nijmegen breakage syndrome", "Ataxia Telangiectasia Variant V1", "Ataxia-Telangiectasia Variant V1s", "Variant V1, Ataxia-Telangiectasia", "Variant 1s, Ataxia-Telangiectasia", "Variant V1s, Ataxia-Telangiectasia", "chromosomal breakage-immunodeficiency syndrome", "microcephaly immunodeficiency lymphoreticuloma", "immunodeficiency microcephaly, normal intelligence", "Microcephaly, normal intelligence and immunodeficiency", "microcephaly, normal intelligence and immunodeficiency", "microcephaly, normal intelligence, and immunodeficiency", "microcephaly-immunodeficiency-lymphoreticuloma syndrome", "Microcephaly-immunodeficiency-lymphoid malignancy syndrome", "immunodeficiency, microcephaly, and chromosomal instability", "IMMUNODEFICIENCY, MICROCEPHALY, AND CHROMOSOMAL INSTABILITY", "Immunodeficiency, Microcephaly, And Chromosomal Instability", "immunodeficiency-microcephaly-chromosomal instability syndrome", "Immunodeficiency-microcephaly-chromosomal instability syndrome", "Microcephaly, normal intelligence and immunodeficiency (disorder)", "microcephaly, normal intelligence, and immunodeficiency (diagnosis)", "Nonsyndromal microcephaly autosomal recessive with normal intelligence", "NONSYNDROMAL MICROCEPHALY, AUTOSOMAL RECESSIVE, WITH NORMAL INTELLIGENCE", "Nonsyndromal microcephaly, autosomal recessive, with normal intelligence", "Nonsyndromal Microcephaly, Autosomal Recessive, with Normal Intelligence", "microcephaly with normal intelligence immunodeficiency and lymphoreticular malignancies", "microcephaly with normal intelligence, immunodeficiency, and lymphoreticular malignancies", "MICROCEPHALY WITH NORMAL INTELLIGENCE, IMMUNODEFICIENCY, AND LYMPHORETICULAR MALIGNANCIES", "Microcephaly with Normal Intelligence, Immunodeficiency, and Lymphoreticular Malignancies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nijmegen breakage syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0004164", "names": ["lymphoepithelioma-like acinar prostate adenocarcinoma", "lymphoepithelioma-like variant acinar prostate adenocarcinoma", "Prostate Acinar Adenocarcinoma, Lymphoepithelioma-Like Variant", "acinar prostate adenocarcinoma, lymphoepithelioma-like variant", "Acinar Prostate Adenocarcinoma, Lymphoepithelioma-Like Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphoepithelioma-like acinar prostate adenocarcinoma", "shortest_name_length": 53}
{"curie": "UMLS:C4520894", "names": ["Stage I Rectosigmoid Cancer", "Stage I Rectosigmoid Carcinoma", "Stage I Rectosigmoid Cancer AJCC v6", "Stage I Rectosigmoid Cancer AJCC v7", "Stage I Rectosigmoid Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Rectosigmoid Cancer AJCC v6 and v7", "shortest_name_length": 27}
{"curie": "MONDO:0012852", "names": ["IBD20", "INFLAMMATORY BOWEL DISEASE 20", "inflammatory bowel disease 20", "Inflammatory Bowel Disease 20", "inflammatory bowel disease type 20"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory bowel disease 20", "shortest_name_length": 5}
{"curie": "UMLS:C4054946", "names": ["FSGS Cellular Variant", "Focal Segmental Glomerulosclerosis Cellular Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Focal Segmental Glomerulosclerosis Cellular Variant", "shortest_name_length": 21}
{"curie": "MONDO:0001514", "names": ["Urethrocele", "urethrocele", "URETHROCELE", "Urethrocoele", "urethra prolapse", "prolapse urethra", "Urethral prolapse", "urethra; prolapse", "urethral prolapse", "prolapse; urethra", "prolapse urethral", "Prolapse;urethral", "URETHRA, PROLAPSE", "Prolapse of urethra", "prolapse of urethra", "urethral urethrocele", "urethrocele (diagnosis)", "urinary meatus; prolapse", "prolapse; urinary meatus", "urethral prolapse (diagnosis)", "Prolapse of urethra (disorder)", "urethrocele (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prolapse of urethra", "shortest_name_length": 11}
{"curie": "UMLS:C4520732", "names": ["stage IV melanoma", "Stage IV Melanoma of Skin", "Stage IV Cutaneous Melanoma", "Stage IV Melanoma of the Skin", "Stage IV Skin Melanoma AJCC v7", "Stage IV Skin Melanoma AJCC v6", "Stage IV Malignant Skin Melanoma", "Stage IV Cutaneous (Skin) Melanoma", "Stage IV Malignant Melanoma of Skin", "Stage IV Cutaneous Malignant Melanoma", "Malignant Melanoma (of Skin), Stage IV", "Stage IV Malignant Melanoma of the Skin", "Stage IV Cutaneous Melanoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Cutaneous Melanoma AJCC v6 and v7", "shortest_name_length": 17}
{"curie": "UMLS:C4521755", "names": ["Stage IV Gastric (Stomach) Cancer", "Clinical Stage IV Gastric Cancer AJCC v8", "Clinical Stage IV Gastric Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage IV Gastric Cancer AJCC v8", "shortest_name_length": 33}
{"curie": "MONDO:0012885", "names": ["CDG1Q", "CDGIq", "CDG Iq", "CDG-Iq", "SRD5A3-CDG", "SRD5A3-CDG (CDG-Iq)", "CDG syndrome type Iq", "congenital disorder of glycosylation 1q", "congenital disorder of glycosylation Iq", "SRD5A3-congenital disorder of glycosylation", "Congenital disorder of glycosylation type Iq", "congenital disorder of glycosylation type 1q", "congenital disorder of glycosylation type Iq", "Congenital disorder of glycosylation type 1q", "congenital disorder of glycosylation, type Iq", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iq", "Congenital disorder of glycosylation type 1q (disorder)", "Congenital disorder of glycosylation type 1q (diagnosis)", "SRD5A3-CDG - steroid 5 alpha-reductase 3 congenital disorder of glycosylation", "Coloboma, Ocular, And Ichthyosis, Brain Malformations, And Endocrine Abnormalities", "coloboma, ocular, with ichthyosis, brain malformations, and endocrine abnormalities", "COLOBOMA, OCULAR, WITH ICHTHYOSIS, BRAIN MALFORMATIONS, AND ENDOCRINE ABNORMALITIES", "congenital disorder of glycosylation due to steroid 5alpha-reductase type 3 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SRD5A3-congenital disorder of glycosylation", "shortest_name_length": 5}
{"curie": "UMLS:C2985351", "names": ["Pregnancy Mood Swing", "Pregnancy Related Mood Swing"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pregnancy Mood Swing", "shortest_name_length": 20}
{"curie": "UMLS:C0375028", "names": ["Acute gonococcal infection of upper genitourinary tract", "Acute Gonococcal Infection of Upper Genitourinary Tract", "acute gonococcal infections of upper genitourinary tract", "Acute gonococcal infection, of upper genitourinary tract", "Gonococcal infection (acute) of upper genitourinary tract", "acute gonococcal infections of upper genitourinary tract (diagnosis)", "Acute gonococcal infection of upper genitourinary tract, site unspecified", "Gonococcal infection (acute) of upper genitourinary tract, site unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute gonococcal infection, of upper genitourinary tract", "shortest_name_length": 55}
{"curie": "MONDO:0013159", "names": ["MDDGB1", "congenital muscular dystrophy-POMT1 related", "muscular dystrophy, congenital, Pomt1-related", "MUSCULAR DYSTROPHY, CONGENITAL, POMT1-RELATED", "muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 1", "muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B1", "muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B, 1", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH IMPAIRED INTELLECTUAL DEVELOPMENT), TYPE B, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B1", "shortest_name_length": 6}
{"curie": "MONDO:0016321", "names": ["pig", "PIG", "pulmonary interstitial glycogenosis", "Pulmonary interstitial glycogenosis", "PIG - Pulmonary interstitial glycogenosis", "Infantile cellular interstitial pneumonitis", "infantile cellular interstitial pneumonitis", "Pulmonary interstitial glycogenosis (disorder)", "pulmonary interstitial glycogenosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary interstitial glycogenosis", "shortest_name_length": 3}
{"curie": "UMLS:C5419894", "names": ["Extranodal Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue Involving the Digestive System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extranodal Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue Involving the Digestive System", "shortest_name_length": 101}
{"curie": "MONDO:0006049", "names": ["Papillary Lung Adenocarcinoma", "Lung Papillary Adenocarcinoma", "lung papillary adenocarcinoma", "lung papillary-adenocarcinoma", "papillary lung adenocarcinoma", "Papillary adenocarcinoma of lung", "papillary adenocarcinoma of lung", "Papillary Adenocarcinoma of Lung", "Papillary Adenocarcinoma of the Lung", "papillary adenocarcinoma of the lung", "Papillary adenocarcinoma of the lung", "primary papillary adenocarcinoma of lung", "Primary papillary adenocarcinoma of lung", "Papillary adenocarcinoma of lung (disorder)", "papillary adenocarcinoma of lung (diagnosis)", "lung malignant adenocarcinoma papillary primary", "Primary papillary adenocarcinoma of lung (disorder)", "primary papillary adenocarcinoma of lung (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papillary lung adenocarcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0010236", "names": ["MRX14", "XLID14", "X-linked mental retardation 14", "Mental retardation, X-linked 14", "mental retardation, X-linked 14", "MENTAL RETARDATION, X-LINKED 14", "intellectual disability, X-linked 14", "X-linked mental retardation 14 (MRX14, XLMR14)", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 14", "non-syndromic X-linked intellectual disability 14", "Mental retardation, X-linked nonspecific, type 14", "mental retardation, X-linked nonspecific, type 14", "intellectual disability, X-linked nonspecific, type 14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 14", "shortest_name_length": 5}
{"curie": "MONDO:0043862", "names": ["Hypophonia", "weak voice", "hypophonia", "Soft voice", "Weak voice", "Quiet voice", "VOICE FATIGUE", "Vocal fatigue", "Voice Fatigue", "vocal fatigue", "Voice fatigue", "voice; defect", "fatigue voice", "voice problem", "defect; voice", "Problem;voice", "voice disorder", "Abnormal voice", "Fatigue, Voice", "Voice Disorder", "ABNORMAL VOICE", "fatigue; voice", "Voice Fatigues", "Disorder;voice", "voice; fatigue", "voice weakness", "voice; disorder", "VOICE DISORDERS", "Vocal disorders", "Voice Disorders", "Voice disorders", "Fatigues, Voice", "disorder; voice", "voice disorders", "Voice alteration", "VOICE ALTERATION", "defective; voice", "Voice impairment", "Disorder of voice", "Weakness of voice", "voice disturbance", "disorder of voice", "Voice Disturbance", "Voice disturbance", "problem with voice", "Voice disturbances", "Disturbance, Voice", "phonation disorder", "Voice Disturbances", "Voice disorder, NOS", "Disturbances, Voice", "Hypophonia (finding)", "neurologic dysphonia", "weak voice (symptom)", "Neurologic dysphonia", "Voice impairment, NOS", "Subenergetic phonation", "Voice disturbance, NOS", "Vocal fatigue (finding)", "Voice disorder syndrome", "Abnormal voice (finding)", "Decreased vocal loudness", "Neurologic voice disorder", "Neurologic Voice Disorder", "neurologic voice disorder", "Neurologic dysphonia, NOS", "Voice Disorder, Neurologic", "NEUROLOGIC VOICE DISORDERS", "Neurologic Voice Disorders", "Voice Disorders, Neurologic", "speech phonation hypophonia", "disease (or disorder); voice", "hypophonia (physical finding)", "voice disturbance (diagnosis)", "Neurologic voice disorder, NOS", "Voice disturbance, unspecified", "Neurologic voice disorder (disorder)", "Neurologic voice disorder (diagnosis)", "disorder speech and language neurologic voice"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "voice disorders", "shortest_name_length": 10}
{"curie": "UMLS:C4330556", "names": ["Lip and Oral Cavity Cancer by AJCC v8 Stage", "Lip and Oral Cavity Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lip and Oral Cavity Cancer by AJCC v8 Stage", "shortest_name_length": 43}
{"curie": "MONDO:0010606", "names": ["HERNIA, ANTERIOR DIAPHRAGMATIC", "Hernia, Anterior Diaphragmatic", "hernia, anterior diaphragmatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hernia, anterior diaphragmatic", "shortest_name_length": 30}
{"curie": "MONDO:0016764", "names": ["MAC spectrum", "clinical anophthalmia", "primitive anophthalmia", "isolated pure microphthalmia", "isolated anophthalmia - microphthalmia", "microphthalmia-anophthalmia-coloboma spectrum", "isolated anophthalmia-microphthalmia syndrome", "nonsyndromic anophthalmia-microphthalmia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated anophthalmia-microphthalmia syndrome", "shortest_name_length": 12}
{"curie": "UMLS:C5556293", "names": ["Microsatellite Stable Endometrial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Microsatellite Stable Endometrial Carcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0011396", "names": ["Camisa disease", "Loricrin keratoderma", "LORICRIN KERATODERMA", "loricrin keratoderma", "Vohwinkel ichthyosis syndrome", "VOHWINKEL SYNDROME, VARIANT FORM", "Vohwinkel Syndrome, Variant Form", "Vohwinkel syndrome, variant form", "VOHWINKEL SYNDROME WITH ICHTHYOSIS", "Vohwinkel syndrome with ichthyosis", "Vohwinkel Syndrome with Ichthyosis", "MUTILATING KERATODERMA WITH ICHTHYOSIS", "Mutilating Keratoderma with Ichthyosis", "mutilating keratoderma with ichthyosis", "keratoderma hereditarium mutilans with ichthyosis", "Keratoderma hereditarium mutilans with ichthyosis", "Keratoderma hereditarium mutilans with ichthyosis syndrome", "Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder)", "Keratoderma ichthyosiform dermatosis elevated beta-glucuronidase syndrome", "Keratoderma-ichthyosiform dermatosis-elevated beta-glucuronidase syndrome", "keratoderma-ichthyosiform dermatosis-elevated beta-glucuronidase syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "loricrin keratoderma", "shortest_name_length": 14}
{"curie": "UMLS:C4553874", "names": ["Stage IVA Differentiated Thyroid Gland Cancer", "Stage IVA Differentiated Thyroid Gland Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Differentiated Thyroid Gland Carcinoma AJCC v8", "shortest_name_length": 45}
{"curie": "MONDO:0008140", "names": ["OSSIFIED EAR CARTILAGES", "ossified ear cartilages", "Ossified Ear Cartilages"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ossified ear cartilages", "shortest_name_length": 23}
{"curie": "MONDO:0013995", "names": ["ICP3", "pregnancy related cholestasis 3", "intrahepatic cholestasis of pregnancy 3", "cholestasis, intrahepatic, of pregnancy 3", "CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY 3", "cholestasis, intrahepatic, of pregnancy, 3", "cholestasis, intrahepatic, of pregnancy type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholestasis, intrahepatic, of pregnancy, 3", "shortest_name_length": 4}
{"curie": "MONDO:0017924", "names": ["Yoshimura-Takeshita syndrome", "central nervous system calcification-deafness-tubular acidosis-anemia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system calcification-deafness-tubular acidosis-anemia syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0013853", "names": ["PCH1B", "pontocerebellar hypoplasia type 1B", "pontocerebellar hypoplasia, type 1B", "PONTOCEREBELLAR HYPOPLASIA, TYPE 1B", "EXOSC3 non-syndromic pontocerebellar hypoplasia", "non-syndromic pontocerebellar hypoplasia caused by mutation in EXOSC3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pontocerebellar hypoplasia type 1B", "shortest_name_length": 5}
{"curie": "UMLS:C0854891", "names": ["Relapsed Malignant Pleural Mesothelioma", "Pleural mesothelioma malignant recurrent", "Recurrent Pleural Malignant Mesothelioma", "Malignant Pleural Mesothelioma Recurrent", "Relapsed Malignant Mesothelioma of Pleura", "Relapsed Malignant Mesothelioma of the Pleura"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pleural mesothelioma malignant recurrent", "shortest_name_length": 39}
{"curie": "MONDO:0003628", "names": ["PULMONIC VALVE DISEASE", "pulmonary valve disease", "Pulmonary valve disease", "Pulmonic valve disorder", "Pulmonary valve disorder", "pulmonary valve disorder", "Pulmonary Valve Disorder", "Pulmonary valve disorders", "disease of pulmonary valve", "Pulmonary valve disease NOS", "disorder of pulmonary valve", "Pulmonic valve disorder, NOS", "Pulmonary valvular disorders", "PVD - Pulmonary valve disease", "Pulmonary valve disorder, NOS", "pulmonary valve disease or disorder", "Pulmonary valve disorder (disorder)", "pulmonary valve disorder (diagnosis)", "Pulmonary valve disorder, unspecified", "disease or disorder of pulmonary valve", "disease (or disorder); pulmonary, valve"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary valve disorder", "shortest_name_length": 22}
{"curie": "MONDO:0001172", "names": ["salpingo-ovaritis", "Salpingo-Oophoritis", "salpingo oophoritis", "salpingo-oophoritis", "Salpingo-oophoritis", "SALPINGO OOPHORITIS", "tubo-ovarian abscess", "tubo ovarian abscess", "salpingitis/oophoritis", "Salpingitis/oophoritis", "infection; tubo-ovarian", "tubo-ovarian; infection", "tubo-ovarian; inflammation", "Salpingitis and oophoritis", "inflammation; tubo-ovarian", "tubo-ovarian abscess (disorder)", "salpingo-oophoritis (diagnosis)", "Tubo-Ovarian Inflammatory Disease", "tubo-ovarian inflammatory disease", "Tubo-ovarian inflammatory disease", "tubo-ovarian; disorder, inflammatory", "Salpingitis and oophoritis, unspecified", "Inflammation of ovary and fallopian tube", "Tubo-ovarian inflammatory disease (disorder)", "tubo-ovarian inflammatory disease (diagnosis)", "Salpingitis and oophoritis not specified as acute, subacute, or chronic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "salpingo-oophoritis", "shortest_name_length": 17}
{"curie": "MONDO:0042977", "names": ["MFT1", "Brooke-Fordyce Trichoepitheliomas", "trichoepithelioma multiple familial 1", "multiple familial trichoepithelioma 1", "trichoepithelioma, multiple familial, 1", "epithelioma adenoides cysticum of Brooke", "epithelioma, hereditary multiple benign cystic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichoepithelioma, multiple familial, 1", "shortest_name_length": 4}
{"curie": "UMLS:C0677707", "names": ["Stage II Diffuse Mixed Cell Lymphoma", "noncontiguous stage II adult diffuse mixed cell lymphoma", "Non-Contiguous Adult Diffuse Mixed Cell Lymphoma Stage II", "non-contiguous adult diffuse mixed cell lymphoma stage II", "Stage II Non-Contiguous Adult Diffuse Mixed Cell Lymphoma", "Non-Contiguous Stage II Adult Diffuse Mixed Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Non-Contiguous Adult Diffuse Mixed Cell Lymphoma", "shortest_name_length": 36}
{"curie": "MONDO:0010708", "names": ["W syndrome", "W SYNDROME", "w syndrome", "syndrome w", "Syndrome W", "syndromes w", "Pallister W syndrome", "Pallister syndrome 1", "Pallister-W syndrome", "PALLISTER W SYNDROME", "Pallister W syndrome (disorder)", "Pallister W syndrome (diagnosis)", "median cleft upper lip, mental retardation and pugilistic facies", "Median cleft upper lip, mental retardation and pugilistic facies", "median cleft upper lip-mental retardation-pugilistic facies syndrome", "median cleft upper lip, intellectual disability and pugilistic facies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pallister-W syndrome", "shortest_name_length": 10}
{"curie": "UMLS:C4290033", "names": ["46,XX/46,XY Disorders of Sex Development", "46,XX/46,XY Ovotesticular Differences of Sex Development"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XX/46,XY Ovotesticular Differences of Sex Development", "shortest_name_length": 40}
{"curie": "MONDO:0006278", "names": ["Lung Papilloma", "lung papilloma", "Bronchial papilloma", "Bronchial Papilloma", "respiratory papilloma", "Respiratory papilloma", "respiratory papillomas", "Respiratory Tract Papilloma", "respiratory tract papilloma", "Papilloma of Respiratory Tract", "papilloma of respiratory tract", "Papilloma of the Respiratory Tract", "papilloma of the respiratory tract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung papilloma", "shortest_name_length": 14}
{"curie": "MONDO:0022716", "names": ["Chiari malformation type 4", "type IV Chiari malformation", "Chiari malformation type IV", "Chiari type IV malformation", "Arnold-Chiari Malformation, Type 4", "Arnold Chiari malformation type IV", "Type IV Arnold Chiari Malformation", "Type IV Arnold-Chiari Malformation", "type IV Arnold-Chiari malformation", "Arnold Chiari Malformation, Type 4", "Arnold Chiari Malformation, Type IV", "Arnold-Chiari Malformation, Type IV", "Chiari malformation type IV (disorder)", "type IV Chiari malformation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chiari malformation type 4", "shortest_name_length": 26}
{"curie": "MONDO:0002638", "names": ["Ninth cranial nerve tumor", "Ninth Cranial Nerve Tumor", "IXth Cranial Nerve Tumors", "IXth cranial nerve tumors", "Ninth cranial nerve tumors", "Ninth Cranial Nerve Tumors", "Tumor of Ninth Cranial Nerve", "IXth Cranial Nerve Neoplasms", "IXth cranial nerve neoplasms", "Ninth cranial nerve neoplasm", "Ninth Cranial Nerve Neoplasm", "tumor of Ninth cranial nerve", "glossopharyngeal nerve tumor", "Glossopharyngeal Nerve Tumor", "Ninth cranial nerve neoplasms", "Glossopharyngeal Nerve Tumors", "Ninth Cranial Nerve Neoplasms", "glossopharyngeal nerve tumors", "tumor of Glossopharyngeal nerve", "tumor of glossopharyngeal nerve", "Neoplasm of Ninth Cranial Nerve", "neoplasm of ninth cranial nerve", "Tumor of Glossopharyngeal Nerve", "neoplasm of Ninth cranial nerve", "Glossopharyngeal Nerve Neoplasm", "glossopharyngeal nerve neoplasm", "tumor of the Ninth cranial nerve", "Tumor of the Ninth Cranial Nerve", "glossopharyngeal nerve neoplasms", "Glossopharyngeal Nerve Neoplasms", "Neoplasm of Glossopharyngeal Nerve", "Neoplasm of glossopharyngeal nerve", "neoplasm of glossopharyngeal nerve", "Tumor of the Glossopharyngeal Nerve", "Neoplasm of the Ninth Cranial Nerve", "neoplasm of the Ninth cranial nerve", "tumor of the glossopharyngeal nerve", "neoplasm of the glossopharyngeal nerve", "Neoplasm of the Glossopharyngeal Nerve", "glossopharyngeal nerve neoplasm (disease)", "neoplasm of ninth cranial nerve (diagnosis)", "Neoplasm of glossopharyngeal nerve (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glossopharyngeal nerve neoplasm", "shortest_name_length": 25}
{"curie": "MONDO:0024518", "names": ["Reactive thrombocytosis", "reactive thrombocytosis", "secondary thrombocytosis", "Secondary thrombocytosis", "thrombocytosis other reactive", "Reactive thrombocytosis (disorder)", "Reactive thrombocytosis (diagnosis)", "secondary thrombocytosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "reactive thrombocytosis", "shortest_name_length": 23}
{"curie": "UMLS:C4054372", "names": ["Nephrotic Syndrome - PDSS2 Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - PDSS2 Associated", "shortest_name_length": 37}
{"curie": "MONDO:0013465", "names": ["ACHM4", "achromatopsia 4", "Achromatopsia 4", "ACHROMATOPSIA 4", "GNAT2 achromatopsia", "achromatopsia type 4", "achromatopsia caused by mutation in GNAT2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "achromatopsia 4", "shortest_name_length": 5}
{"curie": "MONDO:0022682", "names": ["cennamo gangemi syndrome", "hydrocephalus cataract microphthalmos"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cennamo gangemi syndrome", "shortest_name_length": 24}
{"curie": "MONDO:0009153", "names": ["Ectopia Lentis et Pupillae", "ECTOPIA LENTIS ET PUPILLAE", "ectopia lentis et pupillae", "Ectopia lentis et pupillae", "ECTOPIA LENTIS WITH ECTOPIA OF PUPIL", "Ectopia Lentis with Ectopia of Pupil", "ectopia lentis with ectopia of pupil", "Ectopia lentis et pupillae (disorder)", "ectopia lentis et pupillae (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectopia lentis et pupillae", "shortest_name_length": 26}
{"curie": "MONDO:0019438", "names": ["AL", "amyloidosis AL", "AL amyloidosis", "AL Amyloidoses", "AL Amyloidosis", "AL AMYLOIDOSIS", "al amyloidosis", "Primary amyloidosis", "Primary Amyloidosis", "Primary Amyloidoses", "primary amyloidosis", "amyloidosis primary", "Amyloidosis, Primary", "Amyloidoses, Primary", "Amyloidosis, primary", "AMYLOIDOSIS, PRIMARY", "AMYLOIDOSIS, SYSTEMIC", "Idiopathic amyloidosis", "primary AL amyloidosis", "idiopathic amyloidosis", "systemic AL amyloidsis", "Primary AL amyloidosis", "Systemic AL amyloidsis", "Light-chain amyloidosis", "Light chain amyloidosis", "AMYLOIDOSIS, IDIOPATHIC", "Amyloidosis primary systemic", "Primary systemic amyloidosis", "amyloidosis primary systemic", "Primary Systemic Amyloidosis", "Primary Systemic Amyloidoses", "primary systemic amyloidosis", "Systemic Amyloidoses, Primary", "Amyloidoses, Primary Systemic", "Amyloidosis, Primary Systemic", "Systemic Amyloidosis, Primary", "primary amyloidosis (formerly)", "[OBSOLETE] Primary amyloidosis", "Primary systemic AL amyloidosis", "Amyloid light-chain amyloidosis", "primary amyloidosis (diagnosis)", "primary systemic AL amyloidosis", "Immunoglobulin Light chain Amyloidosis", "Immunoglobulin Light-chain Amyloidosis", "immunoglobulin light chain amyloidosis", "Immunoglobulin Light-chain Amyloidoses", "Amyloidosis, Immunoglobulin Light-chain", "Amyloidosis, Immunoglobulin Light chain", "Primary amyloidosis of light chain type", "Amyloid light-chain amyloidosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AL amyloidosis", "shortest_name_length": 2}
{"curie": "UMLS:C2986961", "names": ["Stage IIA1 Cervical Cancer", "Stage IIA1 Cervical Cancer AJCC v7", "FIGO Stage IIA1 Cervical Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA1 Cervical Cancer AJCC v7", "shortest_name_length": 26}
{"curie": "MONDO:0013755", "names": ["ARCL3B", "PYCR1 deficiency", "De Barsy syndrome B", "DE BARSY SYNDROME B", "cutis laxa type IIIB", "PYCR1 de Barsy syndrome", "PYCR1-related de Barsy syndrome", "cutis laxa type IIIB (diagnosis)", "autosomal recessive cutis laxa type IIIB", "cutis laxa, autosomal recessive, type 3B", "cutis laxa, autosomal recessive, type IIIB", "CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIB", "de Barsy syndrome caused by mutation in PYCR1", "pyrroline-5-carboxylate reductase 1 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PYCR1-related de Barsy syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0030518", "names": ["TTD9", "trichothiodystrophy 9, nonphotosensitive", "TRICHOTHIODYSTROPHY 9, NONPHOTOSENSITIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichothiodystrophy 9, nonphotosensitive", "shortest_name_length": 4}
{"curie": "UMLS:C0855080", "names": ["Stage I Mixed Cellularity Hodgkin Lymphoma", "Stage I Mixed Cellularity Hodgkin's Disease", "Mixed Cellularity Hodgkin's Disease Stage I", "Stage I Mixed Cellularity Hodgkin's Lymphoma", "Mixed Cellularity Hodgkin's Lymphoma Stage I", "Stage I Mixed Cellularity Classical Hodgkin Lymphoma", "Ann Arbor Stage I Mixed Cellularity Classic Hodgkin Lymphoma", "Hodgkin's disease mixed cellularity stage I site unspecified", "Ann Arbor Stage I Mixed Cellularity Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's disease mixed cellularity stage I site unspecified", "shortest_name_length": 42}
{"curie": "MONDO:0008491", "names": ["SPS", "SMS", "Startle Syndrome", "Syndrome, Startle", "stiffman syndrome", "Startle Syndromes", "Stiffman Syndrome", "stiff-man syndrome", "STIFF-MAN SYNDROME", "Syndrome, Stiffman", "Syndromes, Startle", "Stiff-Man syndrome", "Stiff-Man Syndrome", "Stiff man syndrome", "Stiff-man syndrome", "Stiff Man Syndrome", "stiff man syndrome", "Syndrome, Stiff-Man", "mans stiff syndrome", "stiff mans syndrome", "syndrome; stiff man", "Stiff-Baby Syndrome", "STIFF-TRUNK SYNDROME", "Stiff-Baby Syndromes", "Stiff-trunk syndrome", "Stiff Trunk Syndrome", "Stiff-Trunk Syndrome", "Syndrome, Stiff-Baby", "Stiff-Trunk Syndromes", "Stiff Person Syndrome", "STIFF-PERSON syndrome", "stiff-person syndrome", "Stiff person syndrome", "Stiff-person syndrome", "Stiff-Person syndrome", "Stiff Person syndrome", "person stiff syndrome", "Syndromes, Stiff-Baby", "Stiff-Person Syndrome", "stiff person syndrome", "Syndrome, Stiff-Trunk", "STIFF-PERSON SYNDROME", "persons stiff syndrome", "Syndrome, Stiff-Person", "Syndromes, Stiff-Trunk", "Morsch Woltman syndrome", "Moersch-Woltman syndrome", "moersch woltman syndrome", "moersch-woltman syndrome", "Moersch Woltmann Syndrome", "Moersch-Woltmann syndrome", "Moersch-Woltmann Syndrome", "moersch-woltmann syndrome", "Syndrome, Moersch-Woltmann", "Congenital Stiff-Man Syndrome", "Congenital Stiff Man Syndrome", "Congenital Stiff-Man Syndromes", "Syndrome, Congenital Stiff-Man", "stiff man syndrome (diagnosis)", "Stiff person spectrum disorder", "Stiff-Man Syndrome, Congenital", "Stiff-Man Syndromes, Congenital", "Syndromes, Congenital Stiff-Man", "Congenital Stiff-Person Syndrome", "Congenital Stiff-Person Syndromes", "Syndrome, Congenital Stiff-Person", "Stiff-Person Syndrome, Congenital", "Gamma neuron overactivity syndrome", "Syndromes, Congenital Stiff-Person", "Stiff-Person Syndromes, Congenital", "Subacute myoclonic spinal neuronitis", "MUSCULAR RIGIDITY AND SPASM, PROGRESSIVE", "Stiff person spectrum disorder (disorder)", "Progressive encephalomyelitis with rigidity", "Stiff person syndrome and related disorders", "progressive encephalomyelitis with rigidity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stiff-person syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0005476", "names": ["atrioventricular node disease", "atrioventricular node disorder", "disease of atrioventricular node", "disorder of atrioventricular node", "atrioventricular node disease or disorder", "disease or disorder of atrioventricular node"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrioventricular node disorder", "shortest_name_length": 29}
{"curie": "UMLS:C0948052", "names": ["allergy chemical", "allergy chemicals", "allergies chemical", "allergies chemicals", "Allergy to chemicals", "Allergy to chemicals NOS", "chemical hypersensitivity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Allergy to chemicals", "shortest_name_length": 16}
{"curie": "UMLS:C5557426", "names": ["Ovarian Sex Cord-Stromal Tumor, NOS", "Ovarian Sex Cord-Stromal Tumor, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Sex Cord-Stromal Tumor, Not Otherwise Specified", "shortest_name_length": 35}
{"curie": "MONDO:0044335", "names": ["soft tissue tumor benign", "soft tissue benign tumor", "benign soft tissue tumor", "Benign Soft Tissue Tumor", "Benign soft tissue tumor", "SOFT TISSUE TUMOR BENIGN", "Soft tissue tumor, benign", "Benign soft tissue tumour", "Soft tissue tumour, benign", "benign soft tissue neoplasm", "Benign Tumor of Soft Tissue", "Benign tumor of soft tissue", "benign tumor of soft tissue", "Benign soft tissue neoplasm", "Neoplasm benign;soft tissue", "Benign Soft Tissue Neoplasm", "Soft tissue neoplasms benign", "soft tissue neoplasm, benign", "Benign tumour of soft tissue", "Benign neoplasm of soft tissue", "Benign Neoplasm of Soft Tissue", "benign neoplasm of soft tissue", "benign tumor of the soft tissue", "Benign soft tissue neoplasm NOS", "Benign neoplasm of soft tissues", "Benign Tumor of the Soft Tissue", "benign neoplasm of the soft tissue", "Benign Neoplasm of the Soft Tissue", "benign soft tissue neoplasm (diagnosis)", "Benign neoplasm of soft tissue (disorder)", "Soft tissue tumor, benign (morphologic abnormality)", "Benign neoplasm of connective and other soft tissues", "Benign neoplasm of connective and other soft tissues, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign soft tissue neoplasm", "shortest_name_length": 24}
{"curie": "MONDO:0012991", "names": ["KHRZ", "KAHRIZI SYNDROME", "Kahrizi Syndrome", "Kahrizi syndrome", "intellectual disability, Kahrizi type", "intellectual disability-cataract-coloboma-kyphosis syndrome", "Mental Retardation, Cataract, Coloboma, and Kyphosis, Autosomal Recessive", "mental retardation, cataract, coloboma, and kyphosis, autosomal recessive", "MENTAL RETARDATION, CATARACT, COLOBOMA, AND KYPHOSIS, AUTOSOMAL RECESSIVE", "intellectual disability, cataract, coloboma, and kyphosis, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kahrizi syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C1336215", "names": ["Stage IIIA Small Cell Lung Cancer", "Stage IIIA Small Cell Lung Carcinoma", "Stage IIIA Small Cell Carcinoma of Lung", "Stage IIIA Small Cell Carcinoma of the Lung", "Stage IIIA Lung Small Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Lung Small Cell Carcinoma AJCC v7", "shortest_name_length": 33}
{"curie": "MONDO:0021471", "names": ["benign endometrium tumor", "Benign Endometrial Tumor", "benign endometrial tumor", "Benign Endometrium Tumor", "Benign Tumor of Endometrium", "Benign Endometrium Neoplasm", "benign endometrial neoplasm", "benign tumor of endometrium", "Benign Endometrial Neoplasm", "endometrium benign neoplasm", "benign endometrium neoplasm", "Benign Neoplasm of Endometrium", "Benign neoplasm of endometrium", "benign neoplasm of endometrium", "benign tumor of the endometrium", "Benign Tumor of the Endometrium", "Benign Neoplasm of the Endometrium", "benign neoplasm of the endometrium", "Benign neoplasm of endometrium (disorder)", "benign neoplasm of endometrium (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of endometrium", "shortest_name_length": 24}
{"curie": "MONDO:0004718", "names": ["Xeroderma of eyelid", "xeroderma of eyelid", "Ichthyosis of eyelid", "Xeroderma of eyelid (disorder)", "xeroderma of eyelid (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "xeroderma of eyelid", "shortest_name_length": 19}
{"curie": "MONDO:0016409", "names": ["primary congenital hypothyroidism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary congenital hypothyroidism", "shortest_name_length": 33}
{"curie": "UMLS:C1333032", "names": ["Chronic Adult T-Cell Lymphoma/Leukemia", "Chronic Adult T-Cell Leukemia/Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic Adult T-Cell Leukemia/Lymphoma", "shortest_name_length": 38}
{"curie": "MONDO:0023188", "names": ["Freiberg", "Freiberg disease", "Freiberg's disease", "freiberg's disease", "Freiberg infraction", "infraction; Freiberg", "Freiberg's infraction", "freiberg's infraction", "Kohler's second disease", "Freiberg-Kohler syndrome", "osteochondrosis; Freiberg", "Freiberg; osteochondrosis", "Osteochondrosis of Freilberg", "second metatarsal osteochondrosis", "Second metatarsal osteochondrosis", "Osteochondrosis of second metatarsal", "Osteochondrosis of the metatarsal bone", "Avascular necrosis of the metatarsal bone", "Juvenile osteochondrosis of second metatarsal", "juvenile osteochondrosis of second metatarsal", "Juvenile osteochondrosis of second metatarsal (disorder)", "juvenile osteochondrosis of second metatarsal (diagnosis)", "Osteochondrosis of the metatarsal head, usually the second"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Freiberg disease", "shortest_name_length": 8}
{"curie": "UMLS:C5557176", "names": ["Stage IIIB Cervical Cancer AJCC v9", "Stage IIIB Cervical Carcinoma AJCC v9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Cervical Cancer AJCC v9", "shortest_name_length": 34}
{"curie": "MONDO:0008862", "names": ["MCC2D", "MCC2 DEFICIENCY", "MCC2 Deficiency", "MCC2 deficiency", "MCC 2 deficiency", "3-methylcrotonylglycinuria 2", "3-METHYLCROTONYLGLYCINURIA II", "3-Methylcrotonylglycinuria II", "methylcrotonylglycinuria type 2", "Methylcrotonylglycinuria type 2", "methylcrotonylglycinuria, type 2", "METHYLCROTONYLGLYCINURIA, TYPE II", "Methylcrotonylglycinuria, Type II", "3 alpha methylcrotonylglycinuria 2", "methylcrotonoyl-CoA carboxylase 2 deficiency", "3-methylcrotonyl-CoA carboxylase 2 deficiency", "3-methylcrotonyl CoA carboxylase 2 deficiency", "3-METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY", "3-Methylcrotonyl-CoA Carboxylase 2 Deficiency", "3-METHYLCROTONYL-CoA carboxylase 2 deficiency", "3-Methylcrotonyl-CoA carboxylase 2 deficiency", "3-@METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY", "MCCC2 3-methylcrotonyl-CoA carboxylase deficiency", "3 alpha methylcrotonyl-CoA carboxylase 2 deficiency", "3 alpha methylcrotonyl-coa carboxylase 2 deficiency", "3-methylcrotonyl-CoA carboxylase deficiency caused by mutation in MCCC2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "3-methylcrotonyl-CoA carboxylase 2 deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0009324", "names": ["HND", "Hartnup", "h disease", "H DISEASE", "hart syndrome", "HART SYNDROME", "disease hartnup", "hartnup disease", "HARTNUP DISEASE", "Hartnup disease", "Hartnup Disease", "Hartnup disorder", "Hartnup Disorder", "hartnup disorder", "disease hartnups", "HARTNUP DISORDER", "Hartnup's disease", "H disease (Hartnup)", "aminoaciduria, Hartnup type", "Hartnup disease (diagnosis)", "Aminoaciduria, Hartnup type", "TRYPTOPHAN PYRROLASE DEFICIENCY", "disease (or disorder); H (Hartnup)", "deficiency of tryptophan oxygenase", "Deficiency of tryptophan pyrrolase", "Deficiency of tryptophan oxygenase", "Neutral Amino Acid Transport Defect", "neutral amino acid transport defect", "Neutral amino acid transport defect", "neutral 1 amino acid transport defect", "Neutral Amino Acid Transport Disorder", "Neutral 1 amino acid transport defect", "Transport Disorder, Neutral Amino Acid", "Amino Acid Transport Disorder, Neutral", "Transport Disorder, Neutral Amino Acids", "Deficiency of tryptophan 2,3-dioxygenase", "Disorder of neutral amino acid transport", "Neutral 1 amino acid transport defect (disorder)", "Deficiency of tryptophan 2,3-dioxygenase (disorder)", "PELLAGRA-CEREBELLAR ATAXIA-RENAL AMINOACIDURIA SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hartnup disease", "shortest_name_length": 3}
{"curie": "MONDO:0030973", "names": ["IMD77", "IMMUNODEFICIENCY 77", "immunodeficiency 77"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 77", "shortest_name_length": 5}
{"curie": "MONDO:0018283", "names": ["primary dystroglycanopathy", "primary alpha-dystroglycanopathy", "primary qualitative or quantitative defects of alpha-dystroglycan"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary qualitative or quantitative defects of alpha-dystroglycan", "shortest_name_length": 26}
{"curie": "MONDO:0033645", "names": ["MC4DN11", "mitochondrial complex 4 deficiency, nuclear type 11", "mitochondrial complex IV deficiency, nuclear type 11", "MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 4 deficiency, nuclear type 11", "shortest_name_length": 7}
{"curie": "MONDO:0006330", "names": ["OFMT", "ossifying fibromyxoma", "Ossifying Fibromyxoma", "ossifying fibromyxoid tumor", "Ossifying Fibromyxoid Tumor", "Ossifying fibromyxoid tumor", "ossifying fibromyxoid tumour", "Ossifying fibromyxoid tumour", "ossifying fibromyxoid neoplasm", "Ossifying Fibromyxoid Neoplasm", "Ossifying fibromyxoid tumor (disorder)", "ossifying fibromyxoid tumor (diagnosis)", "ossifying fibromyxoid tumor (morphologic abnormality)", "Ossifying fibromyxoid tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ossifying fibromyxoid tumor", "shortest_name_length": 4}
{"curie": "MONDO:0006999", "names": ["Tooth Disease", "Tooth disease", "teeth disease", "tooth disease", "Disease;teeth", "dental disease", "Dental disease", "Tooth disorder", "Disorder tooth", "Tooth Disorder", "Disease, Tooth", "Tooth Diseases", "tooth disorder", "tooth diseases", "DISORDER TOOTH", "TOOTH DISORDER", "Dental Disease", "Diseases, Tooth", "Dental Diseases", "Dental Disorder", "dental disorder", "Teeth--Diseases", "dental diseases", "Tooth Disorders", "Dental disorder", "DENTAL DISORDER", "Disease, Dental", "dental disorders", "disease of teeth", "Diseases, Dental", "Dental Condition", "Disease of teeth", "disorder of teeth", "Tooth disorder NOS", "Tooth disorder, NOS", "Dental disease, NOS", "DENTAL DISORDER NOS", "Dental disorder NOS", "disease of the teeth", "odontologic disorders", "Disease of teeth, NOS", "calcareous tooth disease", "Tooth disorder (disorder)", "disease of calcareous tooth", "dental disorders (diagnosis)", "disorder of calcareous tooth", "odontologic disorders (diagnosis)", "disease (or disorder); tooth, teeth", "calcareous tooth disease or disorder", "supporting structures; teeth, disorder", "teeth; disorder, supporting structures", "disease or disorder of calcareous tooth", "Disorder of teeth AND/OR supporting structures", "DISEASES OF THE TEETH AND SUPPORTING STRUCTURES", "disease (or disorder); supporting structures of teeth", "Disorder of teeth and supporting structures, unspecified", "Disorder of teeth AND/OR supporting structures (disorder)", "Unspecified disorder of the teeth and supporting structures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tooth disorder", "shortest_name_length": 13}
{"curie": "MONDO:0002355", "names": ["glottis cancer", "Glottis Cancer", "Glottis carcinoma", "CARCINOMA GLOTTIS", "cancer of glottis", "Glottis Carcinoma", "Carcinoma;glottis", "glottis carcinoma", "Carcinoma glottis", "Glottic Carcinoma", "GLOTTIS CARCINOMA", "Cancer of Glottis", "glottic carcinoma", "Glottic carcinoma", "carcinoma of glottis", "Carcinoma of Glottis", "Carcinoma of glottis", "glottic throat cancer", "cancer of the glottis", "Glottic Throat Cancer", "Cancer of the Glottis", "Carcinoma of the Glottis", "carcinoma of the glottis", "Carcinoma of glottis (disorder)", "Carcinoma of glottis (diagnosis)", "malignant glottis neoplasm carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glottis carcinoma", "shortest_name_length": 14}
{"curie": "MONDO:0100064", "names": ["TH deficiency", "tyrosine hydroxylase deficiency", "Tyrosine Hydroxylase Deficiency", "tyrosine Hydroxylase deficiency", "tyrosine 3-monooxygenase deficiency", "Segawa Syndrome, Autosomal Recessive", "Parkinsonism, Infantile, Autosomal Recessive", "Dystonia, Dopa-Responsive, Autosomal Recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tyrosine hydroxylase deficiency", "shortest_name_length": 13}
{"curie": "UMLS:C0948233", "names": ["Febrile infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Febrile infection", "shortest_name_length": 17}
{"curie": "MONDO:0007875", "names": ["LRS", "Larsen", "Larsen syndrome", "LARSEN SYNDROME", "Larsen Syndrome", "larsen syndrome", "larsens syndrome", "Larsen's syndrome", "larsen's syndrome", "dominant larsen syndrome", "dominant Larsen syndrome", "Larsen syndrome (disorder)", "autosomal dominant Larsen syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Larsen syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0700052", "names": ["intersphincteric abscess", "Intersphincteric abscess", "Intersphincteric abscess (disorder)", "Intersphincteric abscess (diagnosis)", "abscess of connective tissue intersphincteric"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intersphincteric abscess", "shortest_name_length": 24}
{"curie": "MONDO:0032808", "names": ["DEE77", "EIEE77", "MCAHS4", "GPIBD19", "early infantile epileptic encephalopathy 77", "epileptic encephalopathy, early infantile, 77", "developmental and epileptic encephalopathy 77", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 77", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 77", "developmental and epileptic encephalopathy, 77", "GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 19", "glycosylphosphatidylinositol biosynthesis defect 19", "MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 4", "multiple congenital anomalies-hypotonia-seizures syndrome 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 77", "shortest_name_length": 5}
{"curie": "UMLS:C4527005", "names": ["Stage IA Retroperitoneal Sarcoma", "Stage IA Retroperitoneal Sarcoma AJCC v8", "Stage IA Soft Tissue Retroperitoneal Sarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Retroperitoneal Sarcoma AJCC v8", "shortest_name_length": 32}
{"curie": "MONDO:0014189", "names": ["ARMD13", "age related macular degeneration 13", "Age-Related Macular Degeneration-13", "CFI age-related macular degeneration", "macular degeneration, age-related, 13", "MACULAR DEGENERATION, AGE-RELATED, 13", "age related macular degeneration type 13", "macular Degeneration, age-related, type 13", "macular degeneration, age-related, 13, susceptibility to", "age-related macular degeneration caused by mutation in CFI"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "age related macular degeneration 13", "shortest_name_length": 6}
{"curie": "MONDO:0007452", "names": ["MODY1", "MODY type 1", "MODY, type I", "MODY, Type 1", "MODY, type 1", "MODY, TYPE 1", "MODY HNF4A related", "diabetes mellitus type 2", "Diabetes Mellitus Type 2", "diabetes mellitus MODY type 1", "Mild Juvenile Diabetes Mellitus", "MILD JUVENILE DIABETES MELLITUS", "mild juvenile diabetes mellitus", "HNF4A monogenic diabetes mellitus", "HNF4a-Associated Monogenic Diabetes", "HNF4A-associated monogenic diabetes", "maturity-onset diabetes of the young type 1", "type 1 maturity-onset diabetes of the young", "maturity onset diabetes of the Young, type 1", "MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 1", "Maturity onset diabetes of the young, type 1", "maturity-onset diabetes of the young, type 1", "Maturity-Onset Diabetes of the Young, Type 1", "maturity-onset diabetes of the young - type 1", "Maturity onset diabetes of the young, type 1 (disorder)", "maturity-onset diabetes of the young - type 1 (diagnosis)", "hepatocyte nuclear Factor 4-Alpha associated monogenic diabetes", "Hepatocyte Nuclear Factor 4-Alpha Associated Monogenic Diabetes", "HNF4A (hepatocyte nuclear factor 4 alpha) monogenic diabetes mellitus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maturity-onset diabetes of the young type 1", "shortest_name_length": 5}
{"curie": "MONDO:0020396", "names": ["anomaly of the tricuspid valve chordae"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anomaly of the tricuspid valve chordae", "shortest_name_length": 38}
{"curie": "UMLS:C0014851", "names": ["Esophagus Cyst", "Esophageal Cyst", "cyst; esophagus", "esophagus; cyst", "Esophageal cyst", "Cyst, Esophageal", "Oesophageal cyst", "Esophageal Cysts", "Cyst of Esophagus", "Cysts, Esophageal", "Cyst of the Esophagus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Cyst", "shortest_name_length": 14}
{"curie": "MONDO:0016056", "names": ["true microcephaly", "primary microcephaly", "microcephaly, primary", "isolated congenital microcephaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated congenital microcephaly", "shortest_name_length": 17}
{"curie": "MONDO:0005714", "names": ["Semilunar tooth", "Hutchinson sign", "Hutchinson Teeth", "Tooth, semilunar", "hutchinson teeth", "MTCT of syphilis", "Hutchinson teeth", "Hutchinsons Teeth", "Hutchinson's sign", "Screwdriver teeth", "teeth; Hutchinson", "Hutchinson's Teeth", "Hutchinson incisor", "Hutchinson's teeth", "Semicircular tooth", "hutchinson's teeth", "Syphilis;congenital", "SYPHILIS CONGENITAL", "congenital syphilis", "syphilis congenital", "Congenital Syphilis", "Teeth, Hutchinson's", "Congenital syphilis", "Crescent-shape tooth", "Syphilis, Congenital", "syphilis; congenital", "hutchinson's incisors", "Hutchinson's incisors", "congenital; syphilitic", "hereditary; syphilitic", "Notched front baby tooth", "Congenital syphilis, NOS", "Syphilitic primary incisor", "Notched front primary tooth", "Hutchinson's sign (disorder)", "Hutchinson; teeth or incisors", "Hutchinson's sign (diagnosis)", "Hutchinson's teeth (disorder)", "Notched front deciduous tooth", "Notched incisors of Hutchinson", "Congenital syphilis (disorder)", "Hutchinson's teeth (diagnosis)", "Notched primary central incisor", "congenital syphilis (diagnosis)", "Unspecified congenital syphilis", "Hutchinson's teeth were observed", "Congenital syphilis, unspecified", "teeth malformed Hutchinson's teeth", "Herpes zoster involving tip of nose", "Hutchinson's teeth (physical finding)", "Congenital Treponema pallidum infection", "mother-to-child transmission of syphilis", "Mother-to-child transmission of syphilis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital syphilis", "shortest_name_length": 15}
{"curie": "UMLS:C2004480", "names": ["Megalocyte", "Macrocytosis", "megalocytosis", "Megalocytosis", "Karyocytomegaly", "KARYOCYTOMEGALY", "Macrocytosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Macrocytosis (morphologic abnormality)", "shortest_name_length": 10}
{"curie": "MONDO:0006159", "names": ["Colorectal GIST", "colorectal gist", "Colorectal Gastrointestinal Stromal Tumor", "colorectal gastrointestinal stromal tumor", "colorectal gastrointestinal stromal tumor (gist)", "colorectal (colon or rectal) gastrointestinal stromal tumor (gist)", "Colorectal (Colon or Rectal) Gastrointestinal Stromal Tumor (GIST)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorectal gastrointestinal stromal tumor", "shortest_name_length": 15}
{"curie": "MONDO:0012413", "names": ["MCOPS5", "OTX2-related eye disorders", "microphthalmia syndromic 5", "syndromic microphthalmia 5", "MICROPHTHALMIA, SYNDROMIC 5", "Microphthalmia, Syndromic 5", "microphthalmia, syndromic 5", "OTX2 syndromic microphthalmia", "Syndromic microphthalmia type 5", "syndromic microphthalmia type 5", "microphthalmia, syndromic type 5", "Syndromic microphthalmia due to OTX2 mutation", "syndromic microphthalmia caused by mutation in OTX2", "syndromic microphthalmia/anophthalmia due to OTX2 mutation", "Syndromic microphthalmia/anophthalmia due to OTX2 mutation", "Syndromic microphthalmia due to orthodenticle homeobox 2 mutation", "retinal dystrophy, early-onset, with or without pituitary dysfunction", "RETINAL DYSTROPHY, EARLY-ONSET, WITH OR WITHOUT PITUITARY DYSFUNCTION", "Syndromic microphthalmia due to orthodenticle homeobox 2 mutation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic microphthalmia type 5", "shortest_name_length": 6}
{"curie": "MONDO:0011302", "names": ["TID17", "IDDM17", "TYPE 1 DIABETES MELLITUS 17", "type 1 diabetes mellitus 17", "Insulin-Dependent Diabetes Mellitus 17", "INSULIN-DEPENDENT DIABETES MELLITUS 17", "insulin-dependent diabetes mellitus 17", "diabetes mellitus, insulin-dependent, 17", "DIABETES MELLITUS, INSULIN-DEPENDENT, 17", "Diabetes Mellitus, Insulin-Dependent, 17"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type 1 diabetes mellitus 17", "shortest_name_length": 5}
{"curie": "MONDO:0013640", "names": ["FRAM", "Fram", "RAMSVPS", "familial retinal arterial macroaneurysm", "Familial retinal arterial macroaneurysm", "FRAM - familial retinal arterial macroaneurysm", "retinal arterial macroaneurysm and supravalvular pulmonic stenosis", "Retinal arterial macroaneurysm and supravalvular pulmonic stenosis", "RETINAL ARTERIAL MACROANEURYSM WITH SUPRAVALVULAR PULMONIC STENOSIS", "Retinal arterial macroaneurysm with supravalvular pulmonic stenosis", "retinal arterial macroaneurysm with supravalvular pulmonic stenosis", "RAMSVPS - retinal arterial macroaneurysm with supravalvular pulmonic stenosis", "Retinal arterial macroaneurysm with supravalvular pulmonic stenosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial retinal arterial macroaneurysm", "shortest_name_length": 4}
{"curie": "UMLS:C4528747", "names": ["Recurrent Atypical Teratoid/Rhabdoid Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Atypical Teratoid/Rhabdoid Tumor", "shortest_name_length": 42}
{"curie": "MONDO:0008416", "names": ["HRZ", "Tys", "Sclerotylosis", "SCLEROTYLOSIS", "HURIEZ syndrome", "HURIEZ SYNDROME", "Huriez syndrome", "Scleroatrophic syndrome", "Keratoderma with scleroatrophy of extremities", "palmoplantar keratoderma-sclerodactyly syndrome", "Palmoplantar keratoderma sclerodactyly syndrome", "Palmoplantar keratoderma-sclerodactyly syndrome", "Scleroatrophic and keratotic dermatosis of limbs", "SCLEROATROPHIC AND KERATOTIC DERMATOSIS OF LIMBS", "Keratoderma with scleroatrophy of the extremities", "Palmoplantar hyperkeratosis-sclerodactyly syndrome", "Palmoplantar hyperkeratosis sclerodactyly syndrome", "palmoplantar hyperkeratosis-sclerodactyly syndrome", "Palmoplantar hyperkeratosis sclerodactyly syndrome (disorder)", "atrophic fibrosis of the skin of the limbs, hypoplasia of nails, and keratodermia of the palms and soles"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "palmoplantar keratoderma-sclerodactyly syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0004325", "names": ["testis thecoma", "thecoma of testis", "testicular thecoma", "Testicular Thecoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular thecoma", "shortest_name_length": 14}
{"curie": "UMLS:C1332846", "names": ["Heart Epithelioid Angioendothelioma", "Cardiac Epithelioid Angioendothelioma", "Heart Epithelioid Hemangioendothelioma", "Epithelioid Angioendothelioma of Heart", "Cardiac Epithelioid Hemangioendothelioma", "Epithelioid Hemangioendothelioma of Heart", "Epithelioid Angioendothelioma of the Heart", "Epithelioid Hemangioendothelioma of the Heart"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiac Epithelioid Hemangioendothelioma", "shortest_name_length": 35}
{"curie": "UMLS:C1167870", "names": ["graft dysfunction", "Graft dysfunction", "dysfunction grafting", "Transplant dysfunction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Graft dysfunction", "shortest_name_length": 17}
{"curie": "MONDO:0007687", "names": ["White hair, premature", "White Hair, Premature", "WHITE HAIR, PREMATURE", "Graying of Hair, Precocious", "graying of hair, precocious", "GRAYING OF HAIR, PRECOCIOUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "graying of hair, precocious", "shortest_name_length": 21}
{"curie": "UMLS:C4520722", "names": ["Stage I Soft Tissue Sarcoma", "stage I adult soft tissue sarcoma", "Stage I Adult Sarcoma of Soft Tissue", "Stage I Adult Sarcoma of the Soft Tissue", "Stage I Adult Soft Tissue Sarcoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Adult Soft Tissue Sarcoma AJCC v7", "shortest_name_length": 27}
{"curie": "UMLS:C3714240", "names": ["Smad4-Related Juvenile Polyposis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Smad4-Related Juvenile Polyposis", "shortest_name_length": 32}
{"curie": "UMLS:C0085394", "names": ["Serratia Infection", "serratia infection", "Serratia infection", "Serratia infections", "Infection, Serratia", "serratia infections", "Serratia Infections", "Infections, Serratia", "Serratia infection NOS", "Serratia infection (diagnosis)", "Bacterial infection with serratia", "Bacterial infection due to Serratia", "Bacterial infection caused by Serratia", "Bacterial infection caused by Serratia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Serratia Infections", "shortest_name_length": 18}
{"curie": "UMLS:C1566590", "names": ["DGF", "Delayed graft function", "Delayed Graft Function", "Graft Function, Delayed"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Delayed Graft Function", "shortest_name_length": 3}
{"curie": "MONDO:0700178", "names": ["Feline Oral Squamous Cell Carcinoma", "feline oral squamous cell carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "feline oral squamous cell carcinoma", "shortest_name_length": 35}
{"curie": "MONDO:0011565", "names": ["AOMS1", "Reaven Syndrome X", "Reaven syndrome X", "Reaven's syndrome", "reaven's syndrome", "METABOLIC SYNDROME", "Metabolic syndrome", "Metabolic Syndrome", "Syndrome X, Reaven", "metabolic syndrome", "syndrome metabolic", "metabolic syndromes", "Metabolic Syndromes", "Syndrome, Metabolic", "Syndromes, Metabolic", "metabolic syndrome x", "METABOLIC SYNDROME X", "metabolic x syndrome", "Metabolic syndrome X", "Metabolic X Syndrome", "metabolic syndrome X", "Metabolic Syndrome X", "X Syndrome, Metabolic", "Syndrome X, Metabolic", "metabolic syndrome 10", "Syndrome, Metabolic X", "Syndrome X (Metabolic)", "Dysmetabolic Syndrome X", "Dysmetabolic syndrome X", "dysmetabolic syndrome X", "dysmetabolic syndrome x", "Cardiometabolic Syndrome", "Syndrome X, Dysmetabolic", "Cardiometabolic syndrome", "metabolic syndrome type X", "Equine metabolic syndrome", "Insulin resistance syndrome", "Insulin Resistance Syndrome X", "syndrome x insulin resistance", "Syndrome X, Insulin Resistance", "Metabolic syndrome X (disorder)", "Metabolic Cardiovascular Syndrome", "Cardiovascular Syndrome, Metabolic", "Syndrome, Metabolic Cardiovascular", "Cardiovascular Syndromes, Metabolic", "dysmetabolic syndrome X (diagnosis)", "abdominal obesity metabolic syndrome", "METABOLIC SYNDROME, PROTECTION AGAINST", "metabolic syndrome, protection against", "ABDOMINAL OBESITY-METABOLIC SYNDROME 1", "abdominal obesity-metabolic syndrome 1", "abdominal obesity-metabolic syndrome quantitative trait locus 1", "ABDOMINAL OBESITY-METABOLIC SYNDROME QUANTITATIVE TRAIT LOCUS 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metabolic syndrome X", "shortest_name_length": 5}
{"curie": "UMLS:C0019553", "names": ["Hip Contracture", "Hip contracture", "contracture hip", "hip contracture", "Hip Contractures", "Contracture, hip", "hip; contracture", "Hip contractures", "contracture; hip", "contracture hips", "Contracture, Hip", "Contractures, Hip", "contracture of hip", "Contracture of hips", "contracture of hip (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hip Contracture", "shortest_name_length": 15}
{"curie": "MONDO:0005974", "names": ["anguillulosis", "Anguillulosis", "Anguilluliases", "Anguilluliasis", "Strongyloidosis", "STRONGYLOIDOSIS", "strongylodiasis", "strongyloidosis", "Strongyloidiases", "STRONGYLOIDIASIS", "strongyloidiasis", "Strongyloidiasis", "STRONGYLOIDES INFECTION", "strongyloides infection", "Infection by Strongyloides", "infection by Strongyloides", "strongyloidiasis (diagnosis)", "disseminated strongyloidiasis", "Disseminated strongyloidiasis", "Strongyloidiasis, unspecified", "disseminated; strongyloidiasis", "strongyloidiasis; disseminated", "Infection by Strongyloides, NOS", "Infection caused by Strongyloides", "Disseminated strongyloidiasis (disorder)", "disseminated strongyloidiasis (diagnosis)", "Infection caused by Strongyloides (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "strongyloidiasis", "shortest_name_length": 13}
{"curie": "MONDO:0006550", "names": ["urethra skin tag", "skin tag of urethra", "Urethra Fibroepithelial Polyp", "urethra fibroepithelial polyp", "urethral fibroepithelial polyp", "Urethral Fibroepithelial Polyp", "urethral Fibroepithelial polyp", "Fibroepithelial Polyp of Urethra", "fibroepithelial polyp of urethra", "fibroepithelial polyp of the urethra", "Fibroepithelial Polyp of the Urethra"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibroepithelial polyp of urethra", "shortest_name_length": 16}
{"curie": "UMLS:C0268744", "names": ["glomerulonephritis focal and segmental proliferative", "Focal AND segmental proliferative glomerulonephritis", "Focal and segmental proliferative glomerulonephritis", "Focal and Segmental Proliferative Glomerulonephritis", "Focal AND segmental proliferative glomerulonephritis (disorder)", "Focal AND segmental proliferative glomerulonephritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Focal AND segmental proliferative glomerulonephritis", "shortest_name_length": 52}
{"curie": "UMLS:C5205731", "names": ["Prostate Inflammatory Myofibroblastic Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Inflammatory Myofibroblastic Tumor", "shortest_name_length": 43}
{"curie": "UMLS:C1332213", "names": ["T Lymphoblastic Lymphoma", "Adult T Lymphoblastic Lymphoma", "Adult Precursor T-Lymphoblastic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult T Lymphoblastic Lymphoma", "shortest_name_length": 24}
{"curie": "MONDO:0012952", "names": ["CRCS9", "COLORECTAL CANCER, SUSCEPTIBILITY TO, 9", "colorectal cancer, susceptibility to, 9", "colorectal cancer, susceptibility to, on chromosome 16Q", "COLORECTAL CANCER, SUSCEPTIBILITY TO, ON CHROMOSOME 16q"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorectal cancer, susceptibility to, 9", "shortest_name_length": 5}
{"curie": "MONDO:0013458", "names": ["HUPRAS", "HUPRA syndrome", "HUPRA SYNDROME", "Hupra syndrome", "hyperuricemia, pulmonary hypertension, renal failure, and alkalosis", "hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome", "Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome", "hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome", "Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome", "Hyperuricaemia, pulmonary hypertension, renal failure, alkalosis syndrome", "HYPERURICEMIA, PULMONARY HYPERTENSION, RENAL FAILURE, AND ALKALOSIS SYNDROME", "hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome", "Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome (disorder)", "hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C0849804", "names": ["Atrophy;cervix;F", "cervical atrophy", "Cervical Atrophy", "Uterine cervix atrophy", "uterine cervical atrophy", "Atrophy of the Uterine Cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine cervical atrophy", "shortest_name_length": 16}
{"curie": "MONDO:0010611", "names": ["HSAS", "HYCX", "XLAS", "HSAS1", "X-linked HSAS", "hydrocephalus x link", "Bickers-Adams syndrome", "X-linked hydrocephalus", "x-linked hydrocephalus", "hydrocephalus, X-linked", "Hydrocephalus, X-linked", "HYDROCEPHALUS, X-LINKED", "x-linked aqueductal stenosis", "X-linked aqueductal stenosis", "Aqueductal stenosis, X-linked", "AQUEDUCTAL STENOSIS, X-LINKED", "aqueductal stenosis, X-linked", "X-linked acqueductal stenosis", "X-linked hydrocephalus syndrome", "X-linked aqueductal stenosis (XLAS)", "X-linked hydrocephalus syndrome (disorder)", "Hydrocephalus with stenosis of the aqueduct of Sylvius", "hydrocephalus with stenosis of the aqueduct of Sylvius", "X-linked hydrocephalus with stenosis of aqueduct of Sylvius", "hydrocephalus with hirschsprung disease, X-linked recessive", "hydrocephalus due to aqueductal stenosis, X-linked recessive", "hydrocephalus due to congenital stenosis of aqueduct of Sylvius", "HYDROCEPHALUS DUE TO CONGENITAL STENOSIS OF AQUEDUCT OF SYLVIUS", "Hydrocephalus due to congenital stenosis of aqueduct of sylvius", "X-linked hydrocephalus with stenosis of the aqueduct of Sylvius", "X-linked hydrocephalus-stenosis of aqueduct of Sylvius sequence", "HSAS1 Hydrocephalus due to congenital stenosis of aqueduct of sylvius 1", "hydrocephalus due to congenital stenosis of aqueduct of Sylvius (HSAS, HYCX)", "HYDROCEPHALUS, X-LINKED, WITH CONGENITAL IDIOPATHIC INTESTINAL PSEUDOOBSTRUCTION", "hydrocephalus, X-linked, with congenital idiopathic intestinal pseudoobstruction", "Hydrocephalus, X-Linked, with Congenital Idiopathic Intestinal Pseudoobstruction", "hydrocephalus with congenital idiopathic intestinal pseudoobstruction, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked hydrocephalus with stenosis of the aqueduct of Sylvius", "shortest_name_length": 4}
{"curie": "UMLS:C4725856", "names": ["Testicular Follicular Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular Follicular Lymphoma", "shortest_name_length": 30}
{"curie": "MONDO:0010773", "names": ["myopathy and diabetes mellitus", "MITOCHONDRIAL MYOPATHY, LIPID TYPE", "mitochondrial myopathy, lipid type", "Mitochondrial Myopathy, Lipid Type", "mitochondrial myopathy with diabetes", "Mitochondrial Myopathy with Diabetes", "MITOCHONDRIAL MYOPATHY WITH DIABETES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy and diabetes mellitus", "shortest_name_length": 30}
{"curie": "MONDO:0030354", "names": ["FSHD3", "facioscapulohumeral muscular dystrophy 3, digenic", "FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 3, DIGENIC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "facioscapulohumeral muscular dystrophy 3, digenic", "shortest_name_length": 5}
{"curie": "MONDO:0011518", "names": ["WDSTS", "Wiedemann Steiner syndrome", "WIEDEMANN-STEINER SYNDROME", "Wiedemann-Steiner syndrome", "Wiedemann Grosse Dibbern syndrome", "Wiedemann Steiner syndrome (disorder)", "Wiedemann Steiner syndrome (diagnosis)", "Growth Deficiency and Mental Retardation with Facial Dysmorphism", "hairy elbows, short stature, Facial Dysmorphism, and developmental delay", "HAIRY ELBOWS, SHORT STATURE, FACIAL DYSMORPHISM, AND DEVELOPMENTAL DELAY", "A syndrome of abnormal facies, short stature, and psychomotor retardation", "Hypertrichosis-short stature-facial dysmorphism-developmental delay syndrome", "hypertrichosis-short stature-facial dysmorphism-developmental delay syndrome", "Hypertrichosis, short stature, facial dysmorphism, developmental delay syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wiedemann-Steiner syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0018302", "names": ["acquired kinky hair syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired kinky hair syndrome", "shortest_name_length": 28}
{"curie": "UMLS:C5420059", "names": ["Sinonasal Leiomyoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Leiomyoma", "shortest_name_length": 19}
{"curie": "MONDO:0007250", "names": ["CAMPD1", "Camptodactyly", "camptodactyly", "streblodactyly", "Streblodactyly", "camptodactylia", "campylodactyly", "Camptodactylia", "Campylodactyly", "STREBLODACTYLY", "Camptodactyly 1", "CAMPTODACTYLY 1", "camptodactyly 1", "familial streblodactyly", "Familial streblodactyly", "Camptodactyly (disorder)", "Camptodactyly congenital", "Congenital Camptodactyly", "congenital camptodactyly", "Congenital camptodactyly", "camptodactyly of fingers", "Congenital streblodactyly", "Congenital campylodactyly", "Congenital camptodactylia", "camptodactyly and knuckle pads", "Camptodactyly And Knuckle Pads", "CAMPTODACTYLY AND KNUCKLE PADS", "crooked little finger, familial", "Crooked little finger, familial", "Minor streblomicrodactyly, familial", "minor streblomicrodactyly, familial", "Permanent flexion of the finger or toe"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "camptodactyly of fingers", "shortest_name_length": 6}
{"curie": "UMLS:C5239292", "names": ["SCR", "Solitary Cutaneous Reticulohistiocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Solitary Cutaneous Reticulohistiocytosis", "shortest_name_length": 3}
{"curie": "MONDO:0011490", "names": ["DPB", "DPb", "PBLT", "Diffuse panbronchiolitis", "diffuse panbronchiolitis", "Panbronchiolitis, diffuse", "PANBRONCHIOLITIS, DIFFUSE", "panbronchiolitis, diffuse", "Diffuse panbronchiolitis (disorder)", "Diffuse panbronchiolitis (diagnosis)", "lower respiratory tract disorders diffuse panbronchiolitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diffuse panbronchiolitis", "shortest_name_length": 3}
{"curie": "MONDO:0003152", "names": ["adult brainstem gliosarcoma", "gliosarcoma, adult brainstem", "Adult Brain Stem Gliosarcoma", "adult brain stem gliosarcoma", "adult brain stem Gliosarcoma", "gliosarcoma, adult brain stem"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult brainstem gliosarcoma", "shortest_name_length": 27}
{"curie": "UMLS:C1291422", "names": ["3-Oxoacid Coa Transferase Deficiency", "Deficiency of 3-oxoacid CoA-transferase", "Deficiency of 3-oxoacid coenzyme A-transferase", "Deficiency of 3-oxoacid coenzyme A-transferase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Deficiency of 3-oxoacid CoA-transferase", "shortest_name_length": 36}
{"curie": "UMLS:C0279094", "names": ["adult AML in remission", "Adult AML in Remission", "Adult ANLL in Remission", "AML in remission, adult", "adult ANLL in remission", "ANLL in remission, adult", "remission, adult acute myeloid leukemia", "Acute Myeloid Leukemia (AML) in Remission", "Adult Acute Myeloid Leukemia in Remission", "adult acute myeloid leukemia in remission", "adult leukemia, acute myeloid in remission", "myeloid leukemia in remission, adult acute", "remission, adult acute myelogenous leukemia", "adult acute myelogenous leukemia in remission", "Adult Acute Myelogenous Leukemia in Remission", "adult leukemia, acute myelogenous in remission", "myelogenous leukemia in remission, adult acute", "remission, adult acute nonlymphocytic leukemia", "Adult Acute Granulocytic Leukemia in Remission", "Adult Acute Myeloblastic Leukemia in Remission", "Adult Acute NonLymphocytic Leukemia in Remission", "adult acute nonlymphocytic leukemia in remission", "adult leukemia, acute nonlymphocytic in remission", "nonlymphocytic leukemia in remission, adult acute", "Adult Acute Non-Lymphocytic Leukemia in Remission", "Adult Acute Non-Lymphoblastic Leukemia in Remission"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Acute Myeloid Leukemia in Remission", "shortest_name_length": 22}
{"curie": "MONDO:0020407", "names": ["CAVC type B", "CAVC-ventricle hypoplasia syndrome", "complete atrioventricular canal type B", "complete atrioventricular canal-ventricle hypoplasia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complete atrioventricular canal-ventricle hypoplasia syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0016593", "names": ["acquired ataxia", "Acquired ataxia", "Acquired ataxia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired ataxia", "shortest_name_length": 15}
{"curie": "MONDO:0010374", "names": ["RP34", "RP 34", "RETINITIS PIGMENTOSA 34", "Retinitis Pigmentosa 34", "retinitis pigmentosa 34", "retinitis pigmentosa type 34"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 34", "shortest_name_length": 4}
{"curie": "UMLS:C3899668", "names": ["Diffuse Astrocytoma", "Childhood Diffuse Astrocytoma", "childhood diffuse astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Diffuse Astrocytoma", "shortest_name_length": 19}
{"curie": "MONDO:0003317", "names": ["metachronous Wilms tumor", "Metachronous Wilms Tumor", "metachronous Wilms' tumor", "Metachronous Kidney Wilms Tumor", "metachronous kidney Wilms' tumor", "Metachronous Kidney Nephroblastoma", "Metachronous Wilms Tumor of the Kidney", "metachronous Wilms tumor of the kidney"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metachronous kidney Wilms' tumor", "shortest_name_length": 24}
{"curie": "MONDO:0002854", "names": ["prostate sarcoma", "sarcoma prostate", "Prostate Sarcoma", "PROSTATE, SARCOMA", "Sarcoma of Prostate", "sarcoma of prostate", "prostate gland sarcoma", "Sarcoma of the Prostate", "sarcoma of the prostate", "sarcoma of prostate gland", "PROSTATIC CANCER, SARCOMA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate sarcoma", "shortest_name_length": 16}
{"curie": "MONDO:0008639", "names": ["vascular helix of umbilical cord", "VASCULAR HELIX OF UMBILICAL CORD"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vascular helix of umbilical cord", "shortest_name_length": 32}
{"curie": "MONDO:0010413", "names": ["MRX95", "XLID95", "mental retardation, X-linked 95", "Mental Retardation, X-Linked 95", "MENTAL RETARDATION, X-LINKED 95", "intellectual disability, X-linked 95", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 95", "mental retardation, X-linked 95, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 95", "shortest_name_length": 5}
{"curie": "MONDO:0032816", "names": ["NEDAHM", "neurodevelopmental disorder with ataxia, hypotonia, and microcephaly", "NEURODEVELOPMENTAL DISORDER WITH ATAXIA, HYPOTONIA, AND MICROCEPHALY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with ataxia, hypotonia, and microcephaly", "shortest_name_length": 6}
{"curie": "MONDO:0019828", "names": ["PSIS", "ectopic neurohypophysis", "Ectopic neurohypophysis", "Ectopic Neurohypophysis", "Ectopic posterior pituitary", "Ectopic Posterior Pituitary", "Pituitary stalk interruption syndrome", "pituitary stalk interruption syndrome", "Pituitary Stalk Interruption Syndrome", "Pituitary stalk interruption syndrome (disorder)", "hypoplastic anterior pituitary, missing stalk, and ectopic posterior pituitary", "Hypoplastic Anterior Pituitary, Missing Stalk, and Ectopic Posterior Pituitary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pituitary stalk interruption syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0008945", "names": ["CPD5", "ataxia; Hunt", "Hunt; ataxia", "Hunt's disease", "Hunt's syndrome", "myoclonus and ataxia", "RAMSAY HUNT SYNDROME", "Ramsay Hunt syndrome", "Spinodentate Atrophy", "SPINODENTATE ATROPHY", "MYOCLONUS AND ATAXIA", "Myoclonus and Ataxia", "Spinodentate atrophy", "dentatorubral atrophy", "Ramsay Hunt syndrome 1", "Cerebellar Dyssynergia", "Dyssynergia, Cerebellar", "Cerebellar Dyssynergias", "Dyssynergias, Cerebellar", "primary dentatum atrophy", "Ramsay Hunt's syndrome 2", "dentate cerebellar ataxia", "Dentate cerebellar ataxia", "Dentate Cerebellar Ataxia", "Dentate Cerebellar Ataxias", "Dentate Cerebellar Atrophy", "Ataxia, Dentate Cerebellar", "Ramsay Hunt's syndrome (2)", "Cerebellar Ataxias, Dentate", "Atrophy, Dentate Cerebellar", "Ramsay Hunt Syndrome type 2", "Ataxias, Dentate Cerebellar", "Cerebellar Atrophy, Dentate", "Ramsay Hunt syndrome type 1", "progressive myoclonus ataxia", "Dentate Cerebellar Atrophies", "Ramsay Hunt Dentate Syndrome", "Ramsay Hunt syndrome - ataxia", "Progressive cerebellar tremor", "Atrophies, Dentate Cerebellar", "progressive cerebellar tremor", "Ramsay Hunt Cerebellar Syndrome", "cerebelloparenchymal disorder 5", "Ramsay Hunt cerebellar syndrome", "Dentato-rubral atrophy syndrome", "cerebelloparenchymal disorder V", "Cerebelloparenchymal Disorder V", "CEREBELLOPARENCHYMAL DISORDER V", "Myoclonic Cerebellar Dyssynergia", "myoclonic cerebellar dyssynergia", "Myoclonic Cerebellar Dyssynergias", "Cerebellar Dyssynergia, Myoclonic", "Dyssynergia, Myoclonic Cerebellar", "Cerebellar Dyssynergias, Myoclonic", "Dyssynergias, Myoclonic Cerebellar", "Dyssynergia Cerebellaris Myoclonica", "Dyssynergia myoclonica cerebellaris", "dyssynergia cerebellaris myoclonica", "Dyssynergia cerebellaris myoclonica", "cerebelloparenchymal disorder type 5", "Dyssynergia Cerebellaris Progressiva", "dyssynergia; cerebellaris myoclonica", "Dyssynergia cerebellaris progressiva", "dyssynergia cerebellaris progressiva", "cerebellaris myoclonica; dyssynergia", "Dentate Nucleus Syndrome, Ramsay Hunt", "Ramsay Hunt syndrome type 1 (formerly)", "Progressive cerebellar tremor (disorder)", "dyssynergia cerebellaris myoclonica; Hunt", "Hunt; dyssynergia cerebellaris myoclonica", "dyssynergia cerebellaris myoclonica of Hunt", "Dyssynergia Cerebellaris Myoclonica Of Hunt", "DYSSYNERGIA CEREBELLARIS MYOCLONICA OF HUNT", "early-onset cerebellar ataxia with myoclonus", "Early onset cerebellar ataxia with myoclonus", "Dyssynergia cerebellaris myoclonica (disorder)", "dyssynergia cerebellaris myoclonica (diagnosis)", "dyssynergia cerebellaris myoclonica; Ramsay-Hunt", "Ramsay-Hunt; dyssynergia cerebellaris myoclonica", "Early onset cerebellar ataxia with myoclonus (disorder)", "early-onset cerebellar ataxia with myoclonus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myoclonic cerebellar dyssynergia", "shortest_name_length": 4}
{"curie": "MONDO:0030474", "names": ["HTX10", "HETEROTAXY, VISCERAL, 10, AUTOSOMAL, WITH MALE INFERTILITY", "heterotaxy, visceral, 10, autosomal, with male infertility"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heterotaxy, visceral, 10, autosomal, with male infertility", "shortest_name_length": 5}
{"curie": "MONDO:0004065", "names": ["mixed cell melanoma of Choroid", "mixed cell melanoma of choroid", "intermediate cell type choroid melanoma", "Choroid Intermediate Cell Type Melanoma", "Intermediate Cell Type Choroid Melanoma", "Intermediate cell type choroid melanoma", "optic choroid intermediate cell type uveal melanoma", "intermediate cell type uveal melanoma of optic choroid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intermediate cell type choroid melanoma", "shortest_name_length": 30}
{"curie": "MONDO:0035149", "names": ["Secondary erythermalgia", "secondary erythromelalgia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary erythromelalgia", "shortest_name_length": 23}
{"curie": "MONDO:0017666", "names": ["Tylosis", "TYLOSIS", "tylosis", "diffuse PPK", "Diffuse PPK", "Unna-Thost Syndrome", "Thost Unna Syndrome", "Thost-Unna Syndrome", "Unna Thost Syndrome", "Syndrome, Unna-Thost", "Syndrome, Thost-Unna", "tylosis; palmaris et plantaris", "palmaris et plantaris; tylosis", "Keratosis Palmaris et Plantaris", "diffuse keratosis palmoplantaris", "Diffuse palmoplantar keratoderma", "Diffuse keratosis palmoplantaris", "diffuse palmoplantar keratoderma", "Palmoplantar keratoderma, diffuse", "Keratoderma, Palmoplantar, Diffuse", "diffuse palmoplantar hyperkeratosis", "Diffuse palmoplantar hyperkeratosis", "Hyperkeratosis, diffuse palmoplantar", "Hereditary diffuse palmoplantar keratoderma", "Hereditary diffuse palmoplantar keratoderma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diffuse palmoplantar keratoderma", "shortest_name_length": 7}
{"curie": "MONDO:0100433", "names": ["ACTB-AST", "ACTB-associated syndromic thrombocytopenia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ACTB-associated syndromic thrombocytopenia", "shortest_name_length": 8}
{"curie": "MONDO:0019865", "names": ["Mosaic trisomy 4", "mosaic trisomy 4", "trisomy 4 mosaicism", "Trisomy 4 mosaicism", "Mosaic trisomy type 4", "Mosaic trisomy 4 syndrome", "Mosaic trisomy chromosome 4", "trisomy 4 mosaicism (diagnosis)", "Mosaic trisomy 4 syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mosaic trisomy 4", "shortest_name_length": 16}
{"curie": "MONDO:0017186", "names": ["diazoxide-resistant hyperinsulinism", "diazoxide-resistant hyperinsulinemic hypoglycemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diazoxide-resistant hyperinsulinism", "shortest_name_length": 35}
{"curie": "UMLS:C2825114", "names": ["Adult Acute Myeloid Leukemia with inv(16)(p13.1q22)", "Acute Myeloid Leukemia (AML) with inv(16)(p13.1q22); CBFB-MYH11", "Adult Acute Myeloid Leukemia with inv(16)(p13.1q22); CBFB-MYH11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Acute Myeloid Leukemia with inv(16)(p13.1q22); CBFB-MYH11", "shortest_name_length": 51}
{"curie": "UMLS:C0334470", "names": ["myxolipoma", "Myxolipoma", "fibromyxolipoma", "Fibromyxolipoma", "adipose tissue myxolipoma", "myxolipoma of fatty tissue", "myxolipoma of fatty tissue (diagnosis)", "Fibromyxolipoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fibromyxolipoma", "shortest_name_length": 10}
{"curie": "UMLS:C4725681", "names": ["Refractory Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Urothelial Carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0019959", "names": ["GLUCAGONOMA", "Glucagonoma", "glucagonoma", "Glucagonomas", "glucagonomas", "Glucagonoma NOS", "alpha Cell Tumor", "Alpha Cell Tumor", "Alpha cell tumor", "Glucagonoma, NOS", "alpha-Cell Tumor", "Tumor, alpha-Cell", "alpha-Cell Tumors", "Alpha cell tumour", "Alpha-cell adenoma", "Alpha cell adenoma", "alpha-Cell Adenoma", "[M]Glucagonoma NOS", "Tumors, alpha-Cell", "Adenoma, alpha Cell", "Adenoma, alpha-Cell", "alpha-Cell Adenomas", "Glucagonoma syndrome", "Glucagonoma Syndrome", "glucagonoma syndrome", "Adenomas, alpha-Cell", "pancreas; glucagonoma", "Syndrome, Glucagonoma", "glucagonoma; pancreas", "Glucagonoma Syndromes", "Pancreatic Glucagonoma", "Syndromes, Glucagonoma", "Glucagonoma (disorder)", "pancreatic glucagonoma", "islet cell glucagonoma", "glucagonoma (diagnosis)", "glucagonoma of pancreas", "Glucagonoma syndrome, NOS", "pancreas; alpha cell tumor", "pancreas; tumor, alpha cell", "Pancreatic Alpha Cell Tumor", "alpha cell; tumor, pancreas", "tumor; alpha cell, pancreas", "Alpha Cell Tumor of Pancreas", "glucagonoma; unspecified site", "Glucagonoma syndrome (disorder)", "Alpha Cell Tumor of the Pancreas", "Pancreatic Glucagon Producing NET", "alpha cell; tumor, unspecified site", "glucagonoma of pancreas (diagnosis)", "Pancreatic Glucagon Producing Tumor", "Glucagon-Producing Islet Cell Tumor", "tumor; alpha cell, unspecified site", "Glucagonoma (morphologic abnormality)", "Glucagon-Producing Tumor of Islet Cells", "Glucagon-Producing Tumor of the Islet Cells", "PANCREAS, ISLET-CELL TUMOR, GLUCAGON-PRODUCING", "Pancreatic Glucagon-Producing Neuroendocrine Tumor", "Pancreatic Glucagon Producing Neuroendocrine Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glucagonoma", "shortest_name_length": 11}
{"curie": "MONDO:0015296", "names": ["cardiac anomalies-heterotaxy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiac anomalies-heterotaxy syndrome", "shortest_name_length": 37}
{"curie": "MONDO:0007639", "names": ["FUNDUS ALBIPUNCTATUS", "fundus albipunctatus", "Fundus albipunctatus", "Fundus Albipunctatus", "Pigmentary retinal dystrophy", "pigmentary retinal dystrophy", "retinitis punctata albescens", "Fundus albipunctatus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fundus albipunctatus", "shortest_name_length": 20}
{"curie": "MONDO:0006120", "names": ["C-Cell Hyperplasia", "C-cell hyperplasia", "hyperplasia; C-cell", "C-cell; hyperplasia", "Thyroid C-cell hyperplasia", "Thyroid C cell hyperplasia", "C-cell hyperplasia diffuse", "C-cell hyperplasia of thyroid", "C-cell hyperplasia of thyroid (disorder)", "C-cell hyperplasia of thyroid (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "C-cell hyperplasia", "shortest_name_length": 18}
{"curie": "UMLS:C4520738", "names": ["Stage 0 NSCLC", "Stage 0 Non-Small Cell Lung Cancer", "Stage 0 Non-Small Cell Lung Carcinoma", "Lung Non-Small Cell Carcinoma in situ", "Stage 0 Non-Small Cell Carcinoma of Lung", "Non-Small Cell Carcinoma in situ of Lung", "Stage 0 Non-Small Cell Lung Cancer AJCC v7", "Stage 0 Non-Small Cell Lung Cancer AJCC v6", "Stage 0 Non-Small Cell Carcinoma of the Lung", "Non-Small Cell Carcinoma in situ of the Lung", "stage 0 non-small cell lung carcinoma in situ", "Stage 0 Lung Non-Small Cell Cancer AJCC v6 and v7", "Stage 0 Non-Small Cell Lung Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Non-Small Cell Lung Cancer AJCC v6 and v7", "shortest_name_length": 13}
{"curie": "MONDO:0007499", "names": ["ear folding", "EAR FOLDING", "Folded ears"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ear folding", "shortest_name_length": 11}
{"curie": "MONDO:0020082", "names": ["dendritic cell tumor", "Dendritic cell neoplasm", "Dendritic cell tumor, NOS", "Dendritic cell sarcoma, NOS", "Dendritic cell neoplasm (disorder)", "Dendritic cell tumor, Not otherwise specified", "Dendritic cell sarcoma, Not otherwise specified", "Dendritic cell neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dendritic cell tumor", "shortest_name_length": 20}
{"curie": "MONDO:0013910", "names": ["HH8", "KISS1R hypogonadotropic hypogonadism", "HYPOGONADOTROPIC HYPOGONADISM 8 WITH OR WITHOUT ANOSMIA", "hypogonadotropic hypogonadism 8 with or without anosmia", "hypogonadotropic hypogonadism caused by mutation in KISS1R"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadotropic hypogonadism 8 with or without anosmia", "shortest_name_length": 3}
{"curie": "EFO:1001515", "names": ["ovarian endometrioid carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian endometrioid carcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0003378", "names": ["Liver Leiomyosarcoma", "liver leiomyosarcoma", "Hepatic Leiomyosarcoma", "hepatic leiomyosarcoma", "Leiomyosarcoma of Liver", "leiomyosarcoma of liver", "Leiomyosarcoma of the Liver", "leiomyosarcoma of the liver", "leiomyosarcoma of the Liver", "leiomyosarcoma of liver (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "liver leiomyosarcoma", "shortest_name_length": 20}
{"curie": "MONDO:0015410", "names": ["nasal dorsum fistula/cyst"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasal dorsum fistula/cyst", "shortest_name_length": 25}
{"curie": "UMLS:C5418878", "names": ["Metastatic Carcinosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Carcinosarcoma", "shortest_name_length": 25}
{"curie": "UMLS:C0578537", "names": ["cavitation lung", "lung cavitation", "cavitations lung", "Cavitation of lung", "Pulmonary cavitation", "pulmonary cavitation", "cavitation pulmonary", "Cavitation of lung (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cavitation of lung", "shortest_name_length": 15}
{"curie": "UMLS:C4682750", "names": ["Tumor Stage (Pathologic)", "Prostate Cancer by AJCC v8 Stage", "Prostate Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Cancer by AJCC v8 Stage", "shortest_name_length": 24}
{"curie": "UMLS:C5420854", "names": ["Ciliary Body Glioneuroma", "Glioneuroma of ciliary body", "Glioneuroma of ciliary body (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Glioneuroma of ciliary body", "shortest_name_length": 24}
{"curie": "UMLS:C0856014", "names": ["MALT Type Extranodal Marginal Zone B-Cell Lymphoma Stage III", "Extranodal Marginal Zone B-Cell Lymphoma (MALT Type) Stage III", "Extranodal marginal zone B-cell lymphoma (MALT type) stage III", "Stage III Extranodal Marginal Zone B-Cell Lymphoma (MALT Type )", "Stage III Extranodal Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue", "Stage III Extranodal Marginal Zone B-Cell Lymphoma of Mucosa-Associated Lymphoid Tissue", "Ann Arbor Stage III Extranodal Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extranodal marginal zone B-cell lymphoma (MALT type) stage III", "shortest_name_length": 60}
{"curie": "MONDO:0005447", "names": ["testis cancer", "Testis cancer", "cancer testis", "Testis Cancer", "Testis Cancers", "Testis--Cancer", "Cancer, Testis", "testis neoplasm", "TESTICLE CANCER", "cancer testicle", "Cancers, Testis", "testicle cancer", "Cancer of Testis", "cancer of testis", "cancer testicles", "Cancer of testis", "testicular tumor", "Testicular Cancer", "testicular cancer", "cancer testicular", "Testicular cancer", "Testicular Cancers", "testicular cancers", "Cancer, Testicular", "neoplasm of testis", "Cancers, Testicular", "Cancer of the Testis", "testicular carcinoma", "cancer of the testis", "Cancer of the Testes", "Testicular Neoplasms", "Neoplasm malig;testis", "TESTIS NEOPLASM MALIGNANT", "Malignant tumor of testis", "malignant testis neoplasm", "Testis neoplasm malignant", "Malignant Tumor of Testis", "malignant tumor of testis", "Malignant Testicular Tumor", "Malignant tumour of testis", "malignant testicular tumor", "malignant neoplasm of testis", "Malignant neoplasm of testis", "Malignant Neoplasm of Testis", "testicular cancer (diagnosis)", "Malignant Tumor of the Testis", "malignant tumor of the testis", "Malignant Testicular Neoplasm", "pediatric testicular neoplasm", "malignant testicular neoplasm", "Testicular neoplasms malignant", "malignant neoplasm of the testis", "childhood neoplasm of the testis", "Malignant neoplasm of testis NOS", "Malignant Neoplasm of the Testis", "Malignant neoplasm of testis, NOS", "malignant neosplasm of the testis", "Malignant tumor of testis (disorder)", "malignant neoplasm of testis (diagnosis)", "Malignant neoplasm of testis, unspecified", "Malignant neoplasm of testis, unspecified whether descended or undescended"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular cancer", "shortest_name_length": 13}
{"curie": "MONDO:0018459", "names": ["hyperglycerolemia", "isolated glycerol kinase deficiency", "nonsyndromic glycerol kinase deficiency", "isolated inborn glycerol kinase deficiency", "nonsyndromic inborn glycerol kinase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated glycerol kinase deficiency", "shortest_name_length": 17}
{"curie": "MONDO:0009213", "names": ["FA3", "FAC", "FACC", "facc", "FANCC", "Fanconi pancytopenia type 3", "FANCONI PANCYTOPENIA, TYPE 3", "Fanconi pancytopenia, type 3", "Fanconi anemia complementation group C", "Fanconi anemia, complementation group C", "FANCONI ANEMIA, COMPLEMENTATION GROUP C", "Fanconi Anemia, Complementation Group C", "Fanconi anemia complementation group type C", "Fanconi Anemia, complementation group type C", "Fanconi anemia complementation group C (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fanconi anemia complementation group C", "shortest_name_length": 3}
{"curie": "UMLS:C1334654", "names": ["Mediastinal Ganglioneuroma", "Ganglioneuroma of mediastinum", "Ganglioneuroma of Mediastinum", "Ganglioneuroma of the Mediastinum", "Benign ganglioneuroma of mediastinum", "Ganglioneuroma of mediastinum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ganglioneuroma of mediastinum", "shortest_name_length": 26}
{"curie": "MONDO:0005471", "names": ["neurally mediated hypotension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurally mediated hypotension", "shortest_name_length": 29}
{"curie": "MONDO:0020212", "names": ["Anterior corneal dystrophy", "anterior corneal dystrophy", "Dystrophy of anterior cornea", "dystrophy of anterior cornea", "superficial corneal dystrophy", "Superficial corneal dystrophy", "anterior corneal dystrophy (diagnosis)", "Dystrophy of anterior cornea (disorder)", "corneal epithelium corneal dystrophy (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "superficial corneal dystrophy", "shortest_name_length": 26}
{"curie": "MONDO:0010092", "names": ["FLPIS", "Filippi syndrome", "FILIPPI syndrome", "FILIPPI SYNDROME", "Filippi syndrome (disorder)", "Filippi syndrome (diagnosis)", "syndactyly-microcephaly-mental retardation syndrome", "Scott craniodigital syndrome with mental retardation", "Scott craniodigital syndrome with intellectual disability", "syndactyly type I with microcephaly and mental retardation", "Syndactyly type I with microcephaly and mental retardation", "SYNDACTYLY, TYPE I, WITH MICROCEPHALY AND MENTAL RETARDATION", "syndactyly, type I, with microcephaly and mental retardation", "Syndactyly, Type I, With Microcephaly And Mental Retardation", "Type 1 syndactyly-microcephaly-intellectual disability syndrome", "type 1 syndactyly-microcephaly-intellectual disability syndrome", "syndactyly type I with microcephaly and intellectual disability", "Type 1 syndactyly, microcephaly, intellectual disability syndrome", "syndactyly, type I, with microcephaly and intellectual disability", "unusual facial appearance, microcephaly, growth and mental retardation and syndactyly", "unusual facial appearance, microcephaly, growth and intellectual disability and syndactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Filippi syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0700064", "names": ["aneuploid", "Aneuploid", "Aneuploids", "Aneuploidy", "aneuploidy", "Aneuploidies", "aneuploidies", "Aneuploidy, NOS", "chromosome number anomaly", "Alteration of chromosome number", "Numerical Chromosomal Alterations", "Aneuploidy (morphologic abnormality)", "Alteration of chromosome number, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aneuploidy", "shortest_name_length": 9}
{"curie": "MONDO:0002253", "names": ["Spondylosis", "SPONDYLOSIS", "spondyloses", "spondylosis", "Spondylosis NOS", "Spondylosis, NOS", "Spondylosis (disorder)", "spondylosis (diagnosis)", "Unspecified spondylosis", "Spondylosis, unspecified", "spondylosis with myelopathy", "Spondylosis of unspecified site", "Lumbar spondylosis with myelopathy", "lumbar spondylosis with myelopathy", "Lumbosacral spondylosis without myelopathy", "lumbosacral spondylosis without myelopathy", "thoracic or lumbar spondylosis with myelopathy", "Thoracic or lumbar spondylosis with myelopathy", "spondylogenic compression of lumbar spinal cord", "Spondylogenic compression of lumbar spinal cord", "spondylogenic compression of thoracic spinal cord", "Spondylogenic compression of thoracic spinal cord", "Lumbosacral spondylosis without myelopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondylosis", "shortest_name_length": 11}
{"curie": "MONDO:0021076", "names": ["Exocrine Pancreas Tumor", "exocrine pancreas tumor", "Pancreatic Exocrine Tumor", "pancreatic exocrine tumor", "Exocrine Pancreas Neoplasm", "tumor of exocrine pancreas", "Tumor of Exocrine Pancreas", "Tumor of exocrine pancreas", "exocrine pancreas neoplasm", "Tumour of exocrine pancreas", "pancreatic exocrine neoplasm", "Pancreatic Exocrine Neoplasm", "neoplasm of exocrine pancreas", "Neoplasm of Exocrine Pancreas", "Tumor of the Exocrine Pancreas", "tumor of the exocrine pancreas", "Neoplasm of the Exocrine Pancreas", "neoplasm of the exocrine pancreas", "exocrine pancreas neoplasm (disease)", "Tumor of exocrine pancreas (disorder)", "neoplasm of exocrine pancreas (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic exocrine neoplasm", "shortest_name_length": 23}
{"curie": "MONDO:0044316", "names": ["THAMY", "thrombocytopenia, anemia, and myelofibrosis", "THROMBOCYTOPENIA, ANEMIA, AND MYELOFIBROSIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombocytopenia, anemia, and myelofibrosis", "shortest_name_length": 5}
{"curie": "UMLS:C0522619", "names": ["Diffuse dysplasia", "Diffuse Dysplasia", "Diffuse dysplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse dysplasia", "shortest_name_length": 17}
{"curie": "MONDO:0013333", "names": ["Small odontoid peg", "odontoid hypoplasia", "Odontoid Hypoplasia", "Odontoid hypoplasia", "ODONTOID HYPOPLASIA", "Small odontoid process", "Odontoid process hypoplasia", "Hypoplastic odontoid process", "Hypoplasia of the odontoid process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "odontoid hypoplasia", "shortest_name_length": 18}
{"curie": "MONDO:0017047", "names": ["infantile axonal neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile axonal neuropathy", "shortest_name_length": 27}
{"curie": "UMLS:C0276252", "names": ["HEPATITIS CMV", "Hepatitis CMV", "hepatitis cmv", "cmv hepatitis", "cytomegalovirus hepatitis", "Cytomegaloviral hepatitis", "Cytomegalovirus hepatitis", "Hepatitis cytomegalovirus", "CMV - Cytomegalovirus hepatitis", "Cytomegalovirus hepatitis (disorder)", "Cytomegalovirus hepatitis (diagnosis)", "Cytomegalic inclusion virus hepatitis", "Hepatitis in cytomegalic inclusion virus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cytomegalovirus hepatitis", "shortest_name_length": 13}
{"curie": "UMLS:C0403566", "names": ["Aplastic bone disease", "Adynamic bone disease", "Adynamic bone disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adynamic bone disease", "shortest_name_length": 21}
{"curie": "MONDO:0016088", "names": ["HPRT deficiency", "HPRT1 deficiency", "hypoxanthine-guanine phosphoribosyltransferase deficiency", "hypoxanthine-guanine phosphoribosyltransferase 1 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypoxanthine-guanine phosphoribosyltransferase deficiency", "shortest_name_length": 15}
{"curie": "MONDO:0016827", "names": ["myopathy-growth delay-intellectual disability-hypospadias syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy-growth delay-intellectual disability-hypospadias syndrome", "shortest_name_length": 66}
{"curie": "MONDO:0019823", "names": ["premature closure of the arterial duct", "premature closure of the patent ductus arteriosus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "premature closure of the arterial duct", "shortest_name_length": 38}
{"curie": "UMLS:C4331269", "names": ["Sacral Chordoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sacral Chordoma", "shortest_name_length": 15}
{"curie": "MONDO:0019430", "names": ["X-linked intellectual disability-ataxia-apraxia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability-ataxia-apraxia syndrome", "shortest_name_length": 56}
{"curie": "UMLS:C4046029", "names": ["Severe Mental Disorder", "Mental Disorder, Severe", "Severe Mental Disorders", "Mental Disorders, Severe"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mental Disorders, Severe", "shortest_name_length": 22}
{"curie": "MONDO:0017193", "names": ["symptomatic form of Coffin-Lowry syndrome in female carriers"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "symptomatic form of Coffin-Lowry syndrome in female carriers", "shortest_name_length": 60}
{"curie": "MONDO:0014217", "names": ["HHT5", "GDF2 related HHT-like syndrome", "GDF2 hereditary hemorrhagic telangiectasia", "telangiectasia, hereditary hemorrhagic, type 5", "TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 5", "hereditary hemorrhagic telangiectasia caused by mutation in GDF2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "telangiectasia, hereditary hemorrhagic, type 5", "shortest_name_length": 4}
{"curie": "MONDO:0004074", "names": ["Ovarian Mucinous Cystadenofibroma", "ovarian mucinous cystadenofibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian mucinous cystadenofibroma", "shortest_name_length": 33}
{"curie": "OMIM:191530", "names": ["Urate-Binding Globulin, Decrease in", "URATE-BINDING GLOBULIN, DECREASE IN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 35}
{"curie": "MONDO:0019893", "names": ["distal deletion 19p", "telomeric deletion 19p", "distal monosomy 19p13.3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal monosomy 19p13.3", "shortest_name_length": 19}
{"curie": "MONDO:0016440", "names": ["Elastofibroma", "elastofibroma", "elastofibromas", "Elastofibroma Dorsi", "elastofibroma dorsi", "Elastofibroma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "elastofibroma dorsi", "shortest_name_length": 13}
{"curie": "MONDO:0016382", "names": ["hereditary poikiloderma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary poikiloderma", "shortest_name_length": 23}
{"curie": "MONDO:0007564", "names": ["PTR", "pilomatrixoma", "PILOMATRICOMA", "pilomatricoma", "PILOMATRIXOMA", "Pilomatrixoma", "Pilomatricoma", "pilomatricomas", "Pilomatrixoma NOS", "Pilomatricoma, NOS", "Pilomatrixoma, NOS", "benign pilomatricoma", "benign pilomatrixoma", "Benign Pilomatricoma", "Benign Pilomatrixoma", "Pilomatrixoma, Benign", "Pilomatricoma, Benign", "PILOMATRIXOMA, BENIGN", "pilomatrixoma, benign", "pilomatricoma, somatic", "Benign Follicular Tumor", "Pilomatrixoma (disorder)", "Benign Hair Follicle Tumor", "Benign Follicular Neoplasm", "Hair follicle tumor benign", "Hair follicle tumour benign", "Benign calcifying epithelioma", "Benign Hair Follicle Neoplasm", "benign hair follicle neoplasm", "HAIR FOLLICLE NEOPLASM, BENIGN", "Malherbe Calcifying Epithelioma", "calcifying epithelioma malherbe", "benign neoplasm of hair follicles", "Calcifying epithelioma of Malherbe", "Calcifying Epithelioma of Malherbe", "calcifying epithelioma of Malherbe", "Calcifying Epitherlioma of Malherbe", "Epithelioma calcificans of Malherbe", "Epithelioma Calcificans Of Malherbe", "EPITHELIOMA CALCIFICANS OF MALHERBE", "epithelioma calcificans of Malherbe", "calcifying Epitherlioma of Malherbe", "Pilomatrixoma (morphologic abnormality)", "Benign calcifying epithelioma of Malherbe"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pilomatrixoma", "shortest_name_length": 3}
{"curie": "MONDO:0011989", "names": ["Leishmaniasis", "leishmaniasis", "leishmaniosis", "Leishmaniosis", "Leishmaniases", "leishmaniases", "Leishmaniasis NOS", "Leishmania Infection", "leishmania infection", "Leishmania infections", "Leishmania; infection", "leishmania infections", "Infection, Leishmania", "infection; Leishmania", "Leishmania Infections", "Infections, Leishmania", "Leishmaniasis (disorder)", "leishmaniasis (diagnosis)", "Leishmaniasis, unspecified", "visceral leishmaniasis (subtype)", "cutaneous leishmaniasis (subtype)", "Post Kala-Azar Dermal Leishmaniasis", "post kala-Azar dermal leishmaniasis", "Post-kala-azar dermal leishmaniasis", "post-kala-azar dermal leishmaniasis", "post-kala-azar dermal infectious disease by leishmaniasis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leishmaniasis", "shortest_name_length": 13}
{"curie": "UMLS:C1706921", "names": ["Fibrous Histiocytoma of Bone", "benign fibrous histiocytoma of bone", "Benign Fibrous Histiocytoma of Bone", "benign fibrous histiocytoma of bone (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign fibrous histiocytoma of bone", "shortest_name_length": 28}
{"curie": "UMLS:C1096106", "names": ["wound complication", "Wound Complication", "Wound complication", "complications wound", "complications wounds", "Wound Healing Disorder", "Wound Healing Complication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wound Complication", "shortest_name_length": 18}
{"curie": "MONDO:0008442", "names": ["Antinolo-Nieto-Borrego syndrome", "spastic paraplegia neuropathy poikiloderma", "Spastic paraplegia neuropathy poikiloderma", "spastic paraplegia with neuropathy and poikiloderma", "Spastic Paraplegia With Neuropathy And Poikiloderma", "spastic paraplegia-neuropathy-poikiloderma syndrome", "SPASTIC PARAPLEGIA WITH NEUROPATHY AND POIKILODERMA", "familial spastic paraplegia with neuropathy and poikiloderma", "Familial spastic paraplegia with neuropathy and poikiloderma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic paraplegia-neuropathy-poikiloderma syndrome", "shortest_name_length": 31}
{"curie": "MONDO:0008670", "names": ["WS1", "Waardenburg syndrome type I", "Waardenburg Syndrome Type I", "Waardenburg syndrome type 1", "Waardenburg Syndrome Type 1", "WAARDENBURG SYNDROME TYPE 1", "WAARDENBURG SYNDROME, TYPE 1", "Waardenburg Syndrome, Type 1", "Waardenburg syndrome, type 1", "Waardenburg's Syndrome Type 1", "Waardenburg's syndrome type 1", "Waardenburg syndrome type 1 (disorder)", "Waardenburg syndrome type I (diagnosis)", "Waardenburg syndrome with dystopia canthorum", "WAARDENBURG SYNDROME WITH DYSTOPIA CANTHORUM", "Waardenburg Syndrome with Dystopia Canthorum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Waardenburg syndrome type 1", "shortest_name_length": 3}
{"curie": "UMLS:C4553665", "names": ["IIIB", "Stage IIIB Cervical Cancer", "Stage IIIB Cervical Cancer AJCC v8", "Stage IIIB Cervical Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Cervical Cancer AJCC v8", "shortest_name_length": 4}
{"curie": "MONDO:0021184", "names": ["BLV infection", "HTLV infection", "BLV infections", "HTLV infections", "HTLV-BLV infection", "HTLV-BLV Infection", "HTLV-BLV Infections", "HTLV-BLV infections", "HTLV BLV Infections", "HTLV BLV infections", "Deltaretrovirus Infection", "Deltaretrovirus infection", "Infection, Deltaretrovirus", "infection, Deltaretrovirus", "Deltaretrovirus Infections", "deltaretrovirus infections", "infections, Deltaretrovirus", "Infections, Deltaretrovirus", "Disease due to Deltaretrovirus", "Disease caused by Deltaretrovirus", "Disease caused by Deltaretrovirus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deltaretrovirus infections", "shortest_name_length": 13}
{"curie": "UMLS:C4524376", "names": ["Recurrent Breast Angiosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Breast Angiosarcoma", "shortest_name_length": 29}
{"curie": "MONDO:0011691", "names": ["ALS3", "ALS3 (diagnosis)", "Amyotrophic Lateral Sclerosis 3", "AMYOTROPHIC LATERAL SCLEROSIS 3", "amyotrophic lateral sclerosis 3", "amyotrophic lateral sclerosis ALS3", "amyotrophic lateral sclerosis type 3", "AMYOTROPHIC LATERAL SCLEROSIS 3 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyotrophic lateral sclerosis type 3", "shortest_name_length": 4}
{"curie": "MONDO:0009377", "names": ["NAGSD", "aga deficiency", "AGA deficiency", "NAGS deficiency", "nags deficiency", "NAGS Deficiency", "Nags deficiency", "NAGS DEFICIENCY", "Hyperammonemia, type III", "Hyperammonaemia, type III", "NAG synthetase deficiency", "Congenital AGA deficiency", "Hyperammonemia, type III (disorder)", "N-Acetylglutamate synthase deficiency", "N-Acetylglutamate Synthase Deficiency", "N-ACETYLGLUTAMATE SYNTHASE DEFICIENCY", "N-acetylglutamate synthase deficiency", "N-Acetylglutamate Synthetase Deficiency", "N-acetylglutamate synthetase deficiency", "N-ACETYLGLUTAMATE SYNTHETASE DEFICIENCY", "Amino acid acetyltransferase deficiency", "N-acetyl glutamate synthetase deficiency", "N-acetylglutamate transferase deficiency", "N acetyl glutamate synthetase deficiency", "NAGS - N-Acetylglutamate synthase deficiency", "N-acetylglutamate synthetase deficiency (diagnosis)", "hyperammonemia due to N-acetylglutamate synthase deficiency", "Hyperammonemia due to N-acetylglutamate synthase deficiency", "Hyperammonemia due to N-Acetylglutamate Synthetase Deficiency", "HYPERAMMONEMIA DUE TO N-ACETYLGLUTAMATE SYNTHETASE DEFICIENCY", "hyperammonemia due to N-acetylglutamate synthetase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperammonemia due to N-acetylglutamate synthase deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0023041", "names": ["ectodermal dysplasia Berlin type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia Berlin type", "shortest_name_length": 32}
{"curie": "UMLS:C1333951", "names": ["Helicobacter Pylori-Related Gastric Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Helicobacter Pylori-Related Gastric Adenocarcinoma", "shortest_name_length": 50}
{"curie": "MONDO:0014883", "names": ["RCM5", "CMH26", "hypertrophic cardiomyopathy 26", "FLNC hypertrophic cardiomyopathy", "hypertrophic cardiomyopathy type 26", "Familial Restrictive Cardiomyopathy 5", "cardiomyopathy, familial restrictive 5", "cardiomyopathy familial hypertrophic 26", "CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 5", "cardiomyopathy, familial restrictive, 5", "cardiomyopathy, familial hypertrophic, 26", "CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26", "Familial Hypertrophic Cardiomyopathy Type 26", "cardiomyopathy, familial hypertrophic, type 26", "hypertrophic cardiomyopathy caused by mutation in FLNC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophic cardiomyopathy 26", "shortest_name_length": 4}
{"curie": "MONDO:0800088", "names": ["MPS I", "MPS1H", "MPSIH", "MPS1-H", "HURLER", "Hurler", "hurler", "MPS I H", "hurlers", "Gargoylism", "gargoylism", "GARGOYLISM", "Gargoylisms", "hurler disease", "Hurler disease", "Hurler Disease", "hurler syndrome", "Hurlers disease", "Hurler syndrome", "hurlers disease", "HURLER SYNDROME", "Disease;Hurlers", "Hurler Syndrome", "Hurler's Disease", "hurlers syndrome", "hurler's disease", "Hurler's disease", "hurler's syndrome", "thompson syndrome", "Thompson syndrome", "Hurler's Syndrome", "Hurler's syndrome", "Disease, Hurler's", "gargoyle syndrome", "Syndrome, Hurler's", "Johnie McL syndrome", "dysostosis multiplex", "Dysostosis multiplex", "lipochondrodystrophy", "Lipochondrodystrophy", "multiplex; dysostosis", "dysostosis; multiplex", "Ellis-Sheldon syndrome", "Hurler-Pfaundler syndrome", "Pfaundler-Hurler syndrome", "Pfaundler-Hurler Syndrome", "Hurler disease MPS type 1H", "Hurler Syndrome Gargoylism", "Gargoylism, Hurler Syndrome", "gargoyle syndrome (diagnosis)", "MUCOPOLYSACCHARIDOSIS TYPE IH", "Mucopolysaccharidosis Type Ih", "Dysostosis multiplex syndrome", "L-iduronidase deficiency, NOS", "Mucopolysaccharidosis Type IH", "Mucopolysaccharidosis type IH", "mucopolysaccharidosis type IH", "Mucopolysaccharidosis type 1H", "Mucopolysaccharidosis Type Ihs", "Type Ih, Mucopolysaccharidosis", "Mucopolysaccharidosis, MPS-I-H", "chondro-osteodystrophy-corneal", "Mucopolysaccharidosis type I-H", "type I-H mucopolysaccharidosis", "Type Ihs, Mucopolysaccharidosis", "Dysostosis multiplex (disorder)", "L-iduronidase deficiency, Hurler type", "mucopolysaccharidosis type 1H (Hurler)", "Mucopolysaccharidosis type I severe form", "MPS 1-H - Mucopolysaccharidosis type I-H", "Mucopolysaccharidosis type I-H (disorder)", "type I-H mucopolysaccharidosis (diagnosis)", "lysosomal storage disease with skeletal involvement", "Lysosomal storage disease with skeletal involvement", "opacities-hepatosplenomegaly mental deficiency syndrome", "dysostotic idiocy-gargoylism-lipochondrodystrophy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lysosomal storage disease with skeletal involvement", "shortest_name_length": 5}
{"curie": "UMLS:C0011574", "names": ["Involutional Depression", "Involutional depression", "involutional depression", "involutional melancholia", "Involutional Melancholia", "Involutional melancholia", "Depression, Involutional", "Melancholia, Involutional", "involutional melancholia (MDD)", "Involutional depression (disorder)", "involutional melancholia (MDD) (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Involutional Depression", "shortest_name_length": 23}
{"curie": "MONDO:0015227", "names": ["isolated limb malformation", "nonsyndromic limb malformation", "non-syndromic limb malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-syndromic limb malformation", "shortest_name_length": 26}
{"curie": "UMLS:C1333801", "names": ["Digestive System Precancerous Condition", "Gastrointestinal Precancerous Condition", "Gastrointestinal Premalignant Condition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Digestive System Precancerous Condition", "shortest_name_length": 39}
{"curie": "MONDO:0014147", "names": ["CLN13", "CLN13 disease", "neuronal ceroid lipofuscinosis 13", "CTSF neuronal ceroid lipofuscinosis", "CEROID LIPOFUSCINOSIS, NEURONAL, 13", "ceroid lipofuscinosis, neuronal, 13", "neuronal ceroid lipofuscinosis type 13", "ceroid lipofuscinosis, neuronal, type 13", "neuronal ceroid lipofuscinosis 13 Kufs type", "ceroid lipofuscinosis, neuronal, 13, Kufs type", "ceroid lipofuscinosis, neuronal, 13 (Kufs type)", "CEROID LIPOFUSCINOSIS, NEURONAL, 13 (KUFS TYPE)", "neuronal ceroid lipofuscinosis caused by mutation in CTSF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuronal ceroid lipofuscinosis 13", "shortest_name_length": 5}
{"curie": "UMLS:C4683739", "names": ["Stage I Mycosis Fungoides and Sezary Syndrome AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Mycosis Fungoides and Sezary Syndrome AJCC v8", "shortest_name_length": 53}
{"curie": "UMLS:C0040797", "names": ["Traumatic bleeding", "Traumatic Hemorrhage", "traumatic hemorrhage", "Traumatic hemorrhage", "Traumatic haemorrhage", "Traumatic hemorrhage (disorder)", "traumatic hemorrhage (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Traumatic hemorrhage", "shortest_name_length": 18}
{"curie": "MONDO:0013876", "names": ["BCC7", "basal cell carcinoma 7", "TP53 skin basal cell carcinoma", "susceptibility to basal cell carcinoma 7", "basal cell carcinoma, susceptibility to, 7", "BASAL CELL CARCINOMA, SUSCEPTIBILITY TO, 7", "basal cell carcinoma, susceptibility to, type 7", "skin basal cell carcinoma caused by mutation in TP53"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "basal cell carcinoma, susceptibility to, 7", "shortest_name_length": 4}
{"curie": "MONDO:0011403", "names": ["LVNC1", "LEFT VENTRICULAR NONCOMPACTION 1", "left ventricular noncompaction 1", "DTNA left ventricular noncompaction", "left ventricular noncompaction type 1", "left ventricular noncompaction caused by mutation in DTNA", "Left Ventricular Noncompaction, Isolated, Autosomal Dominant", "left ventricular noncompaction 1 with or without congenital heart defects", "LEFT VENTRICULAR NONCOMPACTION 1 WITH OR WITHOUT CONGENITAL HEART DEFECTS", "left ventricular noncompaction 1, with or without congenital heart defects", "NONCOMPACTION OF LEFT VENTRICULAR MYOCARDIUM, FAMILIAL ISOLATED, AUTOSOMAL DOMINANT 1", "Noncompaction of Left Ventricular Myocardium, Familial Isolated, Autosomal Dominant 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "left ventricular noncompaction 1", "shortest_name_length": 5}
{"curie": "UMLS:C0280301", "names": ["Hard Palate SCC", "SCC of Hard Palate", "SCC of the Hard Palate", "Hard Palate Squamous Cell Carcinoma", "Squamous Cell Carcinoma of Hard Palate", "Squamous Cell Carcinoma of the Hard Palate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hard Palate Squamous Cell Carcinoma", "shortest_name_length": 15}
{"curie": "MONDO:0014764", "names": ["SPPRS", "SPPRS syndrome", "spastic paraplegia-psychomotor retardation-seizures syndrome", "spastic paraplegia-severe developmental delay-epilepsy syndrome", "SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES", "spastic paraplegia and psychomotor retardation with or without seizures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic paraplegia-severe developmental delay-epilepsy syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0014565", "names": ["CTRCT43", "CATARACT 43", "cataract 43", "cataract type 43", "UNC45B early-onset non-syndromic cataract", "early-onset non-syndromic cataract caused by mutation in UNC45B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 43", "shortest_name_length": 7}
{"curie": "UMLS:C0279566", "names": ["Breast Paget Disease and Intraductal Carcinoma", "Paget disease and intraductal carcinoma of breast", "Paget's Disease and Intraductal Carcinoma of Breast", "Paget's disease and intraductal carcinoma of breast", "Paget's Disease of Breast with Intraductal Carcinoma", "Paget's disease of breast with intraductal carcinoma", "Paget disease and intraductal carcinoma of the breast", "Paget Disease and Intraductal Carcinoma of the Breast", "Paget disease of the breast with intraductal carcinoma", "Paget's disease and intraductal carcinoma of the breast", "Paget's Disease and Intraductal Carcinoma of the Breast", "[M] Paget's disease and intraductal carcinoma of breast", "Paget's Disease of the Breast with Intraductal Carcinoma", "Paget's disease and intraductal carcinoma of breast (diagnosis)", "Paget's disease and intraductal carcinoma of breast (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paget's disease and intraductal carcinoma of breast", "shortest_name_length": 46}
{"curie": "MONDO:0008265", "names": ["PCLD", "PCLD1", "ADPCLD", "polycystic liver disease", "polycystic liver disease 1", "isolated polycystic liver disease", "Isolated polycystic liver disease", "autosomal dominant polycystic liver disease", "Autosomal dominant polycystic liver disease", "Isolated polycystic liver disease (disorder)", "isolated congenital polycystic liver disease", "nonsyndromic polycystic liver disease (disease)", "nonsyndromic congenital polycystic liver disease", "isolated autosomal dominant polycystic liver disease", "polycystic liver disease 1 with or without kidney cysts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polycystic liver disease 1", "shortest_name_length": 4}
{"curie": "MONDO:0021296", "names": ["stage 0is renal pelvis cancer", "Stage 0is Renal Pelvis Cancer", "renal pelvis in situ carcinoma", "stage 0 renal pelvis carcinoma", "renal pelvis carcinoma in situ", "Renal Pelvis Carcinoma in situ", "Kidney Pelvis Carcinoma in situ", "kidney pelvis carcinoma in situ", "Carcinoma in situ of Renal Pelvis", "Stage 0is Kidney Pelvis Carcinoma", "Carcinoma in situ of renal pelvis", "stage 0is kidney pelvis carcinoma", "carcinoma in situ of renal pelvis", "Carcinoma in situ of Kidney Pelvis", "carcinoma in situ of kidney pelvis", "stage 0is carcinoma of renal pelvis", "Stage 0is Carcinoma of Renal Pelvis", "Stage 0is Carcinoma of Kidney Pelvis", "stage 0is carcinoma of kidney pelvis", "carcinoma in situ of the renal pelvis", "stage 0is renal pelvis cancer aJCC v7", "Stage 0is Renal Pelvis Cancer AJCC v7", "Carcinoma in situ of the Renal Pelvis", "Carcinoma in situ of the Kidney Pelvis", "carcinoma in situ of the kidney pelvis", "Stage 0is Carcinoma of the Renal Pelvis", "stage 0is carcinoma of the renal pelvis", "CIS - Carcinoma in situ of renal pelvis", "stage 0is carcinoma of the kidney pelvis", "Stage 0is Carcinoma of the Kidney Pelvis", "Stage 0is Renal Pelvis Urothelial Carcinoma", "stage 0is renal pelvis urothelial carcinoma", "Carcinoma in situ of renal pelvis (disorder)", "carcinoma in situ of renal pelvis (diagnosis)", "stage 0is kidney renal pelvis urothelial cancer", "stage 0is renal pelvis urothelial carcinoma aJCC v7", "Stage 0is Renal Pelvis Urothelial Carcinoma AJCC v7", "transitional cell carcinoma in situ of renal pelvis", "transitional cell carcinoma in situ of renal pelvis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma in situ of renal pelvis", "shortest_name_length": 29}
{"curie": "UMLS:C5421313", "names": ["Maxillofacial Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Maxillofacial Neoplasm", "shortest_name_length": 22}
{"curie": "UMLS:C5446408", "names": ["Lacrimal Gland Epithelial-Myoepithelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lacrimal Gland Epithelial-Myoepithelial Carcinoma", "shortest_name_length": 49}
{"curie": "UMLS:C0564768", "names": ["Genital infection male", "male genital infection", "Male genital infection", "genitals infection male", "genital infections male", "infection; genital organs, male", "Male genital infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Male genital infection", "shortest_name_length": 22}
{"curie": "UMLS:C5206249", "names": ["Refractory Pancreatic Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Pancreatic Adenocarcinoma", "shortest_name_length": 36}
{"curie": "MONDO:0003433", "names": ["water-clear cell adenoma", "Water-Clear Cell Adenoma", "Water-clear cell adenoma", "water-clear cell; adenoma", "adenoma; water-clear cell", "parathyroid gland water-clear cell adenoma", "Parathyroid Gland Water-Clear Cell Adenoma", "water-clear cell adenoma (morphologic abnormality)", "Water-clear cell adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "water-clear cell adenoma", "shortest_name_length": 24}
{"curie": "UMLS:C1708603", "names": ["Keratinizing Paranasal Sinus Squamous Cell Carcinoma", "Paranasal Sinus Keratinizing Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paranasal Sinus Keratinizing Squamous Cell Carcinoma", "shortest_name_length": 52}
{"curie": "MONDO:0009276", "names": ["BSS", "BDPLT1", "Bernard-Soulier", "giant platelet disease", "Giant platelet syndrome", "Giant Platelet Syndrome", "giant platelet syndrome", "Bernard-Soulier syndrome", "syndrome; giant platelet", "giant platelet; syndrome", "bernard soulier syndrome", "Bernard Soulier Syndrome", "BERNARD-SOULIER SYNDROME", "Syndrome, Giant Platelet", "Bernard Soulier syndrome", "Bernard-Soulier Syndrome", "bernard-soulier syndrome", "Syndrome, Bernard-Soulier", "Syndromes, Giant Platelet", "Platelet Syndromes, Giant", "Bernard-Soulier thrombopathy", "thrombopathy, Bernard-Soulier", "Thrombopathy, Bernard-Soulier", "Bernard - Soulier thrombopathy", "BERNARD-SOULIER SYNDROME, TYPE B", "Bernard-Soulier syndrome, type C", "Bernard-Soulier syndrome, type B", "Bernard-Soulier Syndrome, Type B", "BERNARD SOULIER SYNDROME, TYPE B", "BERNARD-SOULIER SYNDROME, TYPE C", "Bernard-Soulier Syndrome, Type C", "giant platelet disorder, isolated", "Bernard-Soulier syndrome, type A1", "BERNARD-SOULIER SYNDROME, TYPE A1", "Giant platelet syndrome (disorder)", "PLATELET GLYCOPROTEIN Ib DEFICIENCY", "BLEEDING DISORDER, PLATELET-TYPE, 1", "Platelet Glycoprotein Ib Deficiency", "Bernard Soulier syndrome (disorder)", "Platelet glycoprotein Ib deficiency", "bleeding disorder, Platelet-type, 1", "Bernard Soulier syndrome (diagnosis)", "Deficiency of Platelet Glycoprotein 1b", "deficiency of platelet glycoprotein 1b", "Platelet Glycoprotein 1b, Deficiency of", "Hemorrhagiparous thrombocytic dystrophy", "Hemorrhagic dystrophic thrombocytopenia", "Platelet glycoprotein 1b, deficiency of", "hemorrhagic dystrophic thrombocytopenia", "Glycoprotein Ib, Platelet, Deficiency Of", "GLYCOPROTEIN Ib, PLATELET, DEFICIENCY OF", "glycoprotein Ib, Platelet, deficiency of", "VON WILLEBRAND FACTOR RECEPTOR DEFICIENCY", "Von Willebrand Factor Receptor Deficiency", "Von Willebrand Factor receptor deficiency", "Bernard-Soulier syndrome, type A1 (recessive)", "macrothrombocytopenia, familial Bernard-Soulier type", "Thrombocytopenia-prolonged bleeding time-giant platelet syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bernard-Soulier syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0016500", "names": ["ASAN", "Acute sensory ataxic GBS", "acute sensory ataxic GBS", "acute sensory ataxic neuropathy", "Acute sensory ataxic neuropathy", "ASAN - acute sensory ataxic neuropathy", "Acute sensory ataxic neuropathy (disorder)", "Acute sensory ataxic Guillain-Barré syndrome", "Guillain-Barre syndrome acute sensory ataxic", "acute sensory ataxic Guillain-Barre syndrome", "acute sensory ataxic Guillain-Barré syndrome", "acute sensory ataxic Guillain-BarrC) syndrome", "acute sensory ataxic Guillain-Barre syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute sensory ataxic neuropathy", "shortest_name_length": 4}
{"curie": "MONDO:0700145", "names": ["Canine Lymphoma", "canine lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canine lymphoma", "shortest_name_length": 15}
{"curie": "MONDO:0011247", "names": ["jejunal atresia with renal adysplasia", "Jejunal atresia with renal adysplasia", "JEJUNAL ATRESIA WITH RENAL ADYSPLASIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "jejunal atresia with renal adysplasia", "shortest_name_length": 37}
{"curie": "UMLS:C0856100", "names": ["Pancreatitis aggravated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatitis aggravated", "shortest_name_length": 23}
{"curie": "UMLS:C3852984", "names": ["Acute Mesenteric Arterial Embolus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Mesenteric Arterial Embolus", "shortest_name_length": 33}
{"curie": "UMLS:C0349746", "names": ["Delusion somatic", "somatic delusion", "Somatic delusion", "DELUSION SOMATIC", "somatic delusions", "Somatic delusion disorder", "somatic delusional disorder", "somatic delusions (physical finding)", "Somatic delusion disorder (disorder)", "somatic delusional disorder (diagnosis)", "Monosymptomatic hypochondriacal psychosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Somatic delusion disorder", "shortest_name_length": 16}
{"curie": "MONDO:0005383", "names": ["PANIC DISORDER", "panic disorder", "Disorder;panic", "Panic Disorder", "Panic disorder", "panic; disorder", "Panic disorders", "disorder; panic", "panic disorders", "Panic Disorders", "Disorder, Panic", "Disorders, Panic", "Panic disorder NOS", "panic anxiety syndrome", "Panic disorder (disorder)", "panic disorder (diagnosis)", "Episodic paroxysmal anxiety disorder", "Panic disorder [episodic paroxysmal anxiety]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "panic disorder", "shortest_name_length": 14}
{"curie": "MONDO:0100439", "names": ["GSD9A2", "GSD IXa2", "glycogen storage disease IXa2", "liver glycogenosis, X-linked, type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease IXa2", "shortest_name_length": 6}
{"curie": "UMLS:C0236022", "names": ["Neoplasm malignant aggravated", "Aggravated Malignant Neoplasm", "NEOPLASM MALIGNANT AGGRAVATED", "Malignant neoplasm aggravated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant neoplasm aggravated", "shortest_name_length": 29}
{"curie": "MONDO:0021834", "names": ["Akaba Hayasaka syndrome", "frontal bossing, cloudy corneae, low nasal ridge, and micrognathia, hypoplastic thorax, and rhizomelic micromelia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Akaba Hayasaka syndrome", "shortest_name_length": 23}
{"curie": "UMLS:C5556661", "names": ["Cervical Squamous Cell Carcinoma, NOS", "Cervical Squamous Cell Carcinoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Squamous Cell Carcinoma, Not Otherwise Specified", "shortest_name_length": 37}
{"curie": "UMLS:C3896653", "names": ["JPFS", "Juvenile Primary Fibromyalgia Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Juvenile Primary Fibromyalgia Syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0010088", "names": ["MSD", "Austin syndrome", "MUCOSULFATIDOSIS", "Mucosulfatidosis", "mucosulfatidosis", "Mucosulphatidosis", "Juvenile Sulfatidosis", "juvenile sulfatidosis", "Juvenile Sulfatidoses", "Sulfatidosis, Juvenile", "Sulfatidoses, Juvenile", "MULTIPLE SULFATASE DEFICIENCY", "multiple sulfatase deficiency", "Multiple sulfatase deficiency", "Multiple Sulfatase Deficiency", "multiple sulphatase deficiency", "Multiple sulphatase deficiency", "Multiple Sulfatase Deficiencies", "Juvenile sulfatidosis Austin type", "Sulfatidosis Juvenile, Austin Type", "Juvenile sulfatidosis, Austin type", "sulfatidosis juvenile, Austin type", "juvenile sulfatidosis, Austin type", "Juvenile sulphatidosis Austin type", "Multiple sulfatase deficiency, NOS", "Sulfatidosis, Juvenile, Austin Type", "multiple sulfatase deficiency (MSD)", "sulfatidosis, juvenile, Austin type", "Juvenile sulphatidosis, Austin type", "SULFATIDOSIS, JUVENILE, AUSTIN TYPE", "Multiple sulfatase deficiency (MSD)", "multiple sulfatase deficiency disease", "Multiple Sulfatase Deficiency Disease", "Multiple Sulphatase Deficiency Disease", "Multiple sulfatase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucosulfatidosis", "shortest_name_length": 3}
{"curie": "MONDO:0004658", "names": ["Breast Ca in situ", "LCIS of the breast", "situ breast cancer", "Breast Cancer in situ", "Breast Cancer Stage 0", "breast cancer stage 0", "In situ Breast Cancer", "Stage 0 Breast Cancer", "breast cancer in situ", "Breast cancer in situ", "in situ breast cancer", "breast carcinoma situ", "stage 0 breast cancer", "breast cancer, stage 0", "in situ carcinoma breast", "Breast Carcinoma In Situ", "stage 0 breast carcinoma", "carcinoma in situ breast", "breast in situ carcinoma", "Stage 0 Breast Carcinoma", "Breast Carcinoma in situ", "breast carcinoma in situ", "carcinoma in situ; breast", "lobular carcinoma in situ", "Lobular Carcinoma in situ", "breast; carcinoma in situ", "Lobular carcinoma in situ", "Carcinoma in situ of Breast", "Carcinoma in situ of breast", "stage 0 carcinoma of breast", "carcinoma in situ of breast", "Stage 0 Carcinoma of Breast", "Lobular Ca in situ of Breast", "breast lobular cancer in situ", "breast carcinoma lobular situ", "stage 0 breast cancer aJCC v6", "lobular breast cancer in situ", "Stage 0 Breast Cancer AJCC v6", "non-invasive breast carcinoma", "stage 0 breast cancer aJCC v7", "breast cancer lobular in situ", "Non-Invasive Breast Carcinoma", "Stage 0 Breast Cancer AJCC v7", "Carcinoma in situ of breast NOS", "stage 0 carcinoma of the breast", "Stage 0 Carcinoma of the Breast", "carcinoma in situ of the breast", "Carcinoma in situ of the Breast", "lobular in situ breast carcinoma", "lobular breast carcinoma in situ", "Lobular Breast Carcinoma In Situ", "Lobular breast carcinoma in situ", "Lobular Ca in situ of the Breast", "Non-Invasive Carcinoma of Breast", "Breast Lobular Carcinoma In Situ", "in situ lobular breast carcinoma", "non-invasive carcinoma of breast", "Non-invasive carcinoma of breast", "stage 0 breast carcinoma in situ", "lobular breast carcinoma, in situ", "Non-Infiltrating Breast Carcinoma", "non-infiltrating breast carcinoma", "breast; carcinoma in situ, lobular", "lobular; carcinoma in situ, breast", "Lobular breast carcinoma (in situ)", "carcinoma in situ; lobular, breast", "Non-Infiltrating Lobular Carcinoma", "Lobular carcinoma in situ of breast", "lobular carcinoma in situ of breast", "Lobular Carcinoma in situ of Breast", "non-infiltrating carcinoma of breast", "Stage 0 Breast Cancer AJCC v6 and v7", "Non-Infiltrating Carcinoma of Breast", "Non-Infiltrating carcinoma of breast", "Non-Invasive Carcinoma of the Breast", "non-invasive carcinoma of the breast", "lobular cancer in situ of the breast", "stage 0 breast cancer aJCC v6 and v7", "Non-Invasive Lobular Breast Carcinoma", "Carcinoma in situ of breast (disorder)", "Lobular Carcinoma In Situ of the Breast", "carcinoma in situ of breast (diagnosis)", "Carcinoma in situ of breast, unspecified", "Non-Invasive Lobular Carcinoma of Breast", "non-infiltrating carcinoma of the breast", "Non-Infiltrating Carcinoma of the Breast", "Non-Infiltrating Lobular Breast Carcinoma", "breast; noninfiltrating lobular carcinoma", "LCIS (lobular carcinoma in situ) of breast", "breast; lobular, noninfiltrating carcinoma", "lobular; carcinoma, noninfiltrating, breast", "breast; carcinoma, lobular, noninfiltrating", "carcinoma; lobular, noninfiltrating, breast", "Non-Infiltrating Lobular Carcinoma of Breast", "Non-Invasive Lobular Carcinoma of the Breast", "Lobular Carcinoma In Situ of the Breast (LCIS)", "Lobular carcinoma in situ of breast (disorder)", "Unspecified type of carcinoma in situ of breast", "lobular carcinoma in situ of breast (diagnosis)", "Non-Infiltrating Lobular Carcinoma of the Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast carcinoma in situ", "shortest_name_length": 17}
{"curie": "MONDO:0013360", "names": ["BCYM2", "brachyolmia type 2", "BRACHYOLMIA TYPE 2", "Brachyolmia type 2", "Brachyolmia Type 2", "Brachyolmia, Maroteaux type", "BRACHYOLMIA, MAROTEAUX TYPE", "Brachyolmia, Maroteaux Type", "brachyolmia, Maroteaux type", "Brachyolmia - Maroteaux type", "Brachyolmia - Maroteaux type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachyolmia, Maroteaux type", "shortest_name_length": 5}
{"curie": "UMLS:C0334667", "names": ["Lymphoid aleukemic leukemia", "lymphoid aleukemic leukemia", "Aleukemic lymphoid leukemia", "leukemia aleukemic lymphoid", "aleukemic lymphoid leukemia", "Aleukemic Lymphoid Leukemia", "Lymphatic aleukemic leukemia", "Aleukemic lymphatic leukemia", "Aleukemic Lymphatic Leukemia", "Aleukaemic lymphoid leukaemia", "Aleukemic lymphocytic leukemia", "leukemia; lymphatic, aleukemic", "lymphatic; leukemia, aleukemic", "Lymphocytic aleukemic leukemia", "Aleukaemic lymphatic leukaemia", "[M]Aleukemic lymphoid leukemia", "Aleukemic Lymphogenous Leukemia", "[M]Aleukaemic lymphoid leukaemia", "Aleukaemic lymphocytic leukaemia", "Aleukemic lymphoid leukemia (disorder)", "aleukemic lymphoid leukemia (diagnosis)", "Aleukemic lymphoid leukemia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aleukemic Lymphoid Leukemia", "shortest_name_length": 27}
{"curie": "MONDO:0019336", "names": ["GS", "gardner syndrome", "Gardner syndrome", "Gardner Syndrome", "GARDNER SYNDROME", "Syndrome, Gardner", "Gardner Syndromes", "Gardners Syndrome", "gardners syndrome", "Gardner's syndrome", "gardner's syndrome", "Gardner's Syndrome", "Syndromes, Gardner", "Syndrome, Gardner's", "Gardner's Syndromes", "Syndromes, Gardner's", "GS - Gardner's syndrome", "POLYPOSIS, INTESTINAL, III", "Gardner syndrome (disorder)", "POLYPOSIS-OSTEOMATOSIS-EPIDERMOID CYST", "intestinal polyposis, osteomas, sebaceous cysts", "polyposis coli and multiple hard and soft tissue tumors"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gardner syndrome", "shortest_name_length": 2}
{"curie": "UMLS:C1402294", "names": ["Primary", "PRIMARY", "Primary Lesion", "primary; lesion", "lesion; primary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Lesion", "shortest_name_length": 7}
{"curie": "UMLS:C0521754", "names": ["Permanent nystagmus", "Permanent Nystagmus", "nystagmus permanent", "Nystagmus, Permanent", "Permanent nystagmus (disorder)", "Permanent nystagmus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Permanent Nystagmus", "shortest_name_length": 19}
{"curie": "UMLS:C0854794", "names": ["Relapsed Liver Cancer", "Recurrent Liver Cancer", "Relapsed Cancer of Liver", "Hepatic cancer recurrent", "Recurrent Liver Carcinoma", "Recurrent Cancer of Liver", "Liver, cancer of, recurrent", "Relapsed Cancer of the Liver", "Recurrent Cancer of the Liver", "Malignant liver tumor recurrent", "Malignant liver tumour recurrent", "Hepatic neoplasm malignant recurrent", "Malignant hepatic neoplasm recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Liver Carcinoma", "shortest_name_length": 21}
{"curie": "UMLS:C1708773", "names": ["Lung Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Melanoma", "shortest_name_length": 13}
{"curie": "MONDO:0003492", "names": ["lacrimal gland epidermoid carcinoma", "epidermoid carcinoma of lacrimal gland", "lacrimal gland squamous cell carcinoma", "squamous cell carcinoma of lacrimal gland", "Epidermoid carcinoma of the lacrimal gland", "epidermoid carcinoma of the lacrimal gland", "squamous cell carcinoma of the lacrimal gland", "lacrimal gland malignant carcinoma squamous cell", "Lacrimal Drainage System Squamous Cell Carcinoma", "squamous cell carcinoma of lacrimal gland (diagnosis)", "Squamous Cell Carcinoma of the Lacrimal Drainage System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lacrimal gland squamous cell carcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C1167854", "names": ["Implant site infection", "Chemoport site infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Implant site infection", "shortest_name_length": 22}
{"curie": "MONDO:0015284", "names": ["Tabatznik syndrome", "heart-hand syndrome 2", "Heart-hand syndrome 2", "Heart-hand syndrome type 2", "heart-hand syndrome type 2", "atriodigital dysplasia type 2", "Atriodigital dysplasia type 2", "Heart-hand syndrome type 2 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heart-hand syndrome type 2", "shortest_name_length": 18}
{"curie": "MONDO:0020135", "names": ["PCH", "Pontocerebellar Hypoplasia", "pontoneocerebellar atrophy", "pontocerebellar hypoplasia", "pontoneocerebllar hypoplasia", "Pontoneocerebellar hypoplasia", "isolated pontocerebellar hypoplasia", "Congenital Pontocerebellar Hypoplasia", "Congenital pontocerebellar hypoplasia", "nonsyndromic pontocerebellar hypoplasia", "Congenital pontocerebellar hypoplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pontocerebellar hypoplasia", "shortest_name_length": 3}
{"curie": "UMLS:C4743662", "names": ["Digestive System Large Cell Neuroendocrine Carcinoma", "Gastrointestinal System Large Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Digestive System Large Cell Neuroendocrine Carcinoma", "shortest_name_length": 52}
{"curie": "UMLS:C4520966", "names": ["Stage III Pancreatic Cancer", "stage III pancreatic cancer", "Pancreatic Cancer Stage III", "Stage III Pancreatic Carcinoma", "Stage III Carcinoma of Pancreas", "Stage III Pancreatic Cancer AJCC v6", "Stage III Pancreatic Cancer AJCC v7", "Stage III Carcinoma of the Pancreas", "Stage III Pancreatic Cancer AJCC v6 and v7", "Stage III Exocrine and Endocrine Pancreatic Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Pancreatic Cancer AJCC v6 and v7", "shortest_name_length": 27}
{"curie": "MONDO:0012890", "names": ["PCH2B", "Pontocerebellar Hypoplasia Type 2B", "pontocerebellar hypoplasia type 2B", "pontocerebellar hypoplasia, type 2B", "PONTOCEREBELLAR HYPOPLASIA, TYPE 2B", "TSEN2 non-syndromic pontocerebellar hypoplasia", "non-syndromic pontocerebellar hypoplasia caused by mutation in TSEN2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pontocerebellar hypoplasia type 2B", "shortest_name_length": 5}
{"curie": "MONDO:0018077", "names": ["Ohara", "Francis", "Yatobyo", "TULAREMIA", "Tularemia", "tularemia", "tularemias", "Tularemias", "tularaemia", "Tularaemia", "rabbit fever", "fever rabbit", "Rabbit fever", "rabbit; fever", "OHARA DISEASE", "Ohara disease", "Deerfly fever", "fever rabbits", "FEVER, RABBIT", "lemming fever", "deerfly fever", "fever; rabbit", "deer-fly fever", "Deer fly fever", "Tularemia, NOS", "Yatobyo (Japan)", "fever; deer fly", "Tularaemia, NOS", "FEVER, DEER FLY", "deer fly; fever", "Ohara's disease", "FRANCIS DISEASE", "O'Hara's disease", "Francis' disease", "Tularemia (disorder)", "Pahvant Valley fever", "Unspecified tularemia", "tularemia (diagnosis)", "Pahvant Valley plague", "Unspecified tularaemia", "Tularemia, unspecified", "Tularaemia, unspecified", "Francisella tularensis infection", "Francisella tularensis Infection", "Francisella tularensis Infections", "infection; Francisella tularensis", "Infection, Francisella tularensis", "Francisella tularensis; infection", "Pasteurella; infection, tularensis", "infection; Pasteurella, tularensis", "Infection by Francisella tularensis", "infection due to Francisella tularensis", "Francisella tularensis infectious disease", "Francisella tularensis disease or disorder", "Francisella tularensis caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tularemia", "shortest_name_length": 5}
{"curie": "UMLS:C1275206", "names": ["Desmoplastic Tricholemmoma", "Desmoplastic trichilemmoma", "Desmoplastic Trichilemmoma", "Desmoplastic trichilemmoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Desmoplastic trichilemmoma", "shortest_name_length": 26}
{"curie": "UMLS:C1096124", "names": ["Meniscus lesion", "Meniscus injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meniscus injury", "shortest_name_length": 15}
{"curie": "MONDO:0700130", "names": ["partial trisomy 21", "segmental duplication", "partial segmental duplication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial segmental duplication", "shortest_name_length": 18}
{"curie": "MONDO:0003599", "names": ["vulvar liposarcoma", "Vulvar Liposarcoma", "liposarcoma of vulva", "mammalian vulva liposarcoma", "liposarcoma of mammalian vulva", "liposarcoma of vulva (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar liposarcoma", "shortest_name_length": 18}
{"curie": "UMLS:C3642327", "names": ["Cervical Endometrioid Stromal Sarcoma", "Endometrioid Stromal Sarcoma of the Cervix", "Cervical Low Grade Endometrioid Stromal Sarcoma", "Low Grade Endometrioid Stromal Sarcoma of the Cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Low Grade Endometrioid Stromal Sarcoma", "shortest_name_length": 37}
{"curie": "MONDO:0004767", "names": ["Vesiculitis", "vesiculitis", "seminal Sacs", "Seminal Sacs", "seminal vertigo", "seminal vesicle", "SEMINAL VESICLE", "Seminal Vesicle", "Vesiculitis NOS", "seminal vesicles", "spermatocystitis", "Seminal Vesicles", "Spermatocystitis", "Seminal Vesiculitis", "SEMINAL VESICULITIS", "Vesiculitis;seminal", "seminal vesiculitis", "Seminal vesiculitis", "Vesiculitis, seminal", "gland, seminal vesicle", "GLAND, SEMINAL VESICLE", "seminal vesicle inflammation", "Seminal vesiculitis (disorder)", "inflammation of seminal vesicle", "seminal vesiculitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vesiculitis", "shortest_name_length": 11}
{"curie": "MONDO:0005459", "names": ["SCHLAFKRANKHEIT", "Sleeping Sickness", "sickness sleeping", "Sleeping sickness", "SLEEPING SICKNESS", "sleeping sickness", "MALADIE DU SOMMEIL", "Sleeping sickness NOS", "Sleeping sickness, NOS", "African Trypanosomiasis", "African Trypanosomiases", "African trypanosomiasis", "trypanosomiasis; African", "Trypanosomiases, African", "Trypanosomiasis, African", "TRYPANOSOMIASIS, AFRICAN", "African; trypanosomiasis", "Africam sleeping sickness", "African Sleeping Sickness", "African sickness sleeping", "African sleeping sickness", "sleeping sickness; African", "Sickness, African Sleeping", "African; sleeping sickness", "SLEEPING SICKNESS, AFRICAN", "Sleeping Sickness, African", "African Sleeping Sicknesses", "Sleeping Sicknesses, African", "Sicknesses, African Sleeping", "human african trypanosomiasis", "human African trypanosomiasis", "African trypanosomiasis (disorder)", "African trypanosomiasis (diagnosis)", "African trypanosomiasis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "human African trypanosomiasis", "shortest_name_length": 15}
{"curie": "MONDO:0007538", "names": ["AI3", "AI3A", "ADHCAI", "Amelogenesis imperfecta type 3", "amelogenesis imperfecta type 3", "FAM83H amelogenesis imperfecta", "amelogenesis imperfecta, type 3", "amelogenesis imperfecta type 3A", "amelogenesis imperfecta, type 3A", "amelogenesis imperfecta type III", "AMELOGENESIS IMPERFECTA, TYPE III", "Amelogenesis Imperfecta, Type III", "amelogenesis imperfecta, type III", "AMELOGENESIS IMPERFECTA, TYPE IIIA", "amelogenesis imperfecta, type IIIA", "hypocalcified amelogenesis imperfecta", "Hypocalcified amelogenesis imperfecta", "Amelogenesis imperfecta - hypocalcified", "Amelogenesis imperfecta - hypomineralization", "Amelogenesis imperfecta - hypomineralisation", "amelogenesis imperfecta hypomineralization type", "Amelogenesis imperfecta, hypocalcification type", "amelogenesis imperfecta, hypomineralization type", "Amelogenesis Imperfecta, Hypomineralization Type", "AMELOGENESIS IMPERFECTA, HYPOMINERALIZATION TYPE", "amelogenesis imperfecta caused by mutation in FAM83H", "Amelogenesis imperfecta, hypocalcification type (disorder)", "autosomal dominant amelogenesis imperfecta hypocalcification type", "amelogenesis imperfecta, hypocalcification type, autosomal dominant", "Amelogenesis Imperfecta, Hypocalcification Type, Autosomal Dominant", "AMELOGENESIS IMPERFECTA, HYPOCALCIFICATION TYPE, AUTOSOMAL DOMINANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amelogenesis imperfecta, type 3A", "shortest_name_length": 3}
{"curie": "UMLS:C1336371", "names": ["stage IVB hypopharyngeal cancer", "Stage IVB Hypopharynx Carcinoma", "Stage IVB Carcinoma of Hypopharynx", "Stage IVB Hypopharyngeal Throat Cancer", "Stage IVB Carcinoma of the Hypopharynx", "Stage IVB Hypopharyngeal Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Hypopharyngeal Carcinoma AJCC v7", "shortest_name_length": 31}
{"curie": "MONDO:0012976", "names": ["DFNA2B", "autosomal dominant deafness 2B", "Deafness, Autosomal Dominant 2B", "deafness, autosomal dominant 2b", "DEAFNESS, AUTOSOMAL DOMINANT 2B", "deafness, autosomal dominant 2B", "deafness, autosomal dominant type 2B", "autosomal dominant nonsyndromic deafness 2B", "GJB3 autosomal dominant nonsyndromic deafness", "autosomal dominant nonsyndromic hearing loss 2B", "autosomal dominant nonsyndromic deafness type 2B", "autosomal dominant nonsyndromic deafness caused by mutation in GJB3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 2B", "shortest_name_length": 6}
{"curie": "MONDO:0008198", "names": ["PFMCCD", "parietal foramina with clavicular hypoplasia", "Parietal foramina with clavicular hypoplasia", "Cleidocranial Dysplasia With Parietal Foramina", "PARIETAL FORAMINA WITH CLEIDOCRANIAL DYSPLASIA", "CLEIDOCRANIAL DYSPLASIA WITH PARIETAL FORAMINA", "Parietal Foramina With Cleidocranial Dysplasia", "cleidocranial dysplasia with parietal foramina", "parietal foramina with cleidocranial dysplasia", "Parietal foramina with cleidocranial dysplasia", "parietal foramina with cleidocranial dysostosis", "Parietal foramina with clavicular hypoplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parietal foramina with cleidocranial dysplasia", "shortest_name_length": 6}
{"curie": "UMLS:C3272521", "names": ["Small Intestinal T-Cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Intestinal T-Cell Non-Hodgkin Lymphoma", "shortest_name_length": 44}
{"curie": "MONDO:0013106", "names": ["BCC6", "basal cell carcinoma, susceptibility to, 6", "BASAL CELL CARCINOMA, SUSCEPTIBILITY TO, 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "basal cell carcinoma, susceptibility to, 6", "shortest_name_length": 4}
{"curie": "MONDO:0004669", "names": ["salivary gland tumor", "tumor salivary gland", "Salivary Gland Tumor", "gland salivary tumor", "salivary gland cancer", "Salivary gland cancer", "cancer salivary gland", "gland salivary tumors", "salivary gland tumour", "Salivary Gland Cancer", "salivary gland cancers", "cancer glands salivary", "Cancer, Salivary Gland", "glands salivary tumors", "gland salivary tumours", "Salivary Gland Cancers", "Tumor of Salivary Gland", "Salivary Gland Neoplasm", "Cancers, Salivary Gland", "Salivary gland neoplasm", "salivary gland neoplasm", "glands salivary tumours", "Salivary glands--Cancer", "Tumor of salivary gland", "Neoplasm, Salivary Gland", "of cancer salivary gland", "Gland Neoplasm, Salivary", "of salivary gland cancer", "Cancer of Salivary Gland", "Cancer of salivary gland", "Tumour of salivary gland", "Salivary Gland Neoplasms", "Salivary gland neoplasia", "cancer of salivary gland", "glands neoplasms salivary", "Salivary gland cancer NOS", "Gland Neoplasms, Salivary", "Neoplasms, Salivary Gland", "neoplasm of salivary gland", "Neoplasm of salivary gland", "Neoplasm of Salivary Gland", "Tumor of the Salivary Gland", "Salivary gland neoplasm NOS", "cancer of the salivary gland", "Cancer of the Salivary Gland", "CA - Cancer of salivary gland", "saliva-secreting gland cancer", "Neoplasm of the Salivary Gland", "Malignant Salivary Gland Tumor", "malignant salivary gland tumor", "Malignant salivary gland cancer", "cancer of saliva-secreting gland", "glands malignant salivary tumors", "malignant salivary gland neoplasm", "Malignant Salivary Gland Neoplasm", "Malignant Tumor of Salivary Gland", "Malignant salivary gland neoplasm", "malignant tumor of salivary gland", "Malignant tumor of salivary gland", "Malignant tumour of salivary gland", "Salivary gland neoplasms malignant", "malignant neoplasm of salivary gland", "Malignant neoplasm of salivary gland", "Malignant Neoplasm of Salivary Gland", "Neoplasm of salivary gland (disorder)", "malignant tumor of the salivary gland", "Malignant Tumor of the Salivary Gland", "neoplasm of salivary gland (diagnosis)", "malignant neoplasm of the salivary gland", "Malignant Neoplasm of the Salivary Gland", "Malignant neoplasm of salivary gland NOS", "malignant neoplasm of salivary gland duct", "malignant saliva-secreting gland neoplasm", "malignant neoplasm of major salivary gland", "Malignant tumor of salivary gland (disorder)", "malignant neoplasm of saliva-secreting gland", "malignant neoplasm of salivary gland (diagnosis)", "Malignant neoplasm of salivary gland, unspecified", "Malignant neoplasm of other major salivary glands", "Malignant neoplasm of other and unspecified major salivary glands"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "salivary gland cancer", "shortest_name_length": 20}
{"curie": "MONDO:0017742", "names": ["disorder of O-xylosylglycan synthesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of O-xylosylglycan synthesis", "shortest_name_length": 37}
{"curie": "MONDO:0008540", "names": ["Hapnes-Boman-Skeie syndrome", "Hapnes Boman Skeie syndrome", "extensor tendons of finger anomalies", "Extensor tendons of finger anomalies", "Extensor tendons of finger anomalies (disorder)", "anomalous insertion of extensor tendons of fingers", "TENDONS, EXTENSOR, OF FINGERS, ANOMALOUS INSERTION OF", "tendons, extensor, of fingers, anomalous insertion OF", "Tendons, Extensor, of Fingers, Anomalous Insertion of", "[OBSOLETE] Tendons, Extensor, of Fingers, Anomalous Insertion of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extensor tendons of finger anomalies", "shortest_name_length": 27}
{"curie": "UMLS:C0474821", "names": ["Coccygeal body tumor", "Coccygeal Body Tumor", "Coccygeal body tumour", "Glomus Coccygeum Tumor", "Coccygeal Body Neoplasm", "Glomus Coccygeum Neoplasm", "neoplasm of coccygeal body", "Neoplasm of coccygeal body", "Neoplasm of coccygeal body (disorder)", "neoplasm of coccygeal body (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplasm of coccygeal body", "shortest_name_length": 20}
{"curie": "MONDO:0007725", "names": ["HISTIOCYTOSIS, PROGRESSIVE MUCINOUS", "histiocytosis, progressive mucinous", "Histiocytosis, Progressive Mucinous", "hereditary progressive mucinous histiocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary progressive mucinous histiocytosis", "shortest_name_length": 35}
{"curie": "UMLS:C1333028", "names": ["Choroid Spindle Cell Type A Melanoma", "Spindle Cell Type A Melanoma of Choroid", "Spindle Cell Type A Melanoma of the Choroid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Choroid Spindle Cell Type A Melanoma", "shortest_name_length": 36}
{"curie": "UMLS:C1332038", "names": ["AIDS-related anal cancer", "AIDS-Related Anal Cancer", "AIDS-Related Anal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Anal Carcinoma", "shortest_name_length": 24}
{"curie": "UMLS:C5419085", "names": ["Advanced Ampulla of Vater Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Ampulla of Vater Carcinoma", "shortest_name_length": 35}
{"curie": "MONDO:0021246", "names": ["Pharynx Tumor", "pharynx tumor", "Pharyngeal Tumor", "Pharynx Neoplasm", "pharyngeal tumor", "pharynx neoplasm", "Tumor of Pharynx", "tumor of pharynx", "Pharyngeal Neoplasm", "neoplasm of pharynx", "Neoplasm of Pharynx", "Tumor of the Pharynx", "Pharyngeal Neoplasms", "pharyngeal neoplasms", "tumor of the pharynx", "neoplasm of the pharynx", "Neoplasm of the Pharynx", "pharynx neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pharynx neoplasm", "shortest_name_length": 13}
{"curie": "UMLS:C0302142", "names": ["Deformity", "deformity", "MALFORMATION", "Deformity (finding)", "Anatomical deformity", "Anatomic Abnormality", "Anatomical Abnormality", "Deformity (morphologic abnormality)", "Congenital or Acquired Anatomic Abnormality", "Congenital or Acquired Anatomical Abnormality"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Deformity", "shortest_name_length": 9}
{"curie": "UMLS:C3501647", "names": ["Glutathione Peroxidase Deficiency, Hemolytic Anemia possibly due to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Glutathione Peroxidase Deficiency, Hemolytic Anemia possibly due to", "shortest_name_length": 67}
{"curie": "UMLS:C4055244", "names": ["Childhood Lymphomatoid Granulomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Lymphomatoid Granulomatosis", "shortest_name_length": 37}
{"curie": "UMLS:C0161479", "names": ["Nerve Injury", "Nerve injury", "Nerve damage", "NERVE DAMAGE", "nerve damage", "nerve injury", "Nerve Damage", "nerve; injury", "injury; nerve", "neural injury", "Injury;nerve(s)", "Nerve injury NOS", "Nerve injury, NOS", "Nerve damage, NOS", "Nerve injury (disorder)", "nerve injury (diagnosis)", "Injury to nerves, unspecified site", "nerve injury in unspecified body part", "Injuries to nerves, nerve plexuses and roots", "Injury of nerve(s) of unspecified body region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nerve injury", "shortest_name_length": 12}
{"curie": "UMLS:C5554613", "names": ["Microsatellite Stable Rectal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Microsatellite Stable Rectal Carcinoma", "shortest_name_length": 38}
{"curie": "UMLS:C4683618", "names": ["Lymphoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoma by AJCC v8 Stage", "shortest_name_length": 25}
{"curie": "MONDO:0017513", "names": ["split foot, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "split foot, unilateral", "shortest_name_length": 22}
{"curie": "MONDO:0010247", "names": ["ALD", "adrenoleukodystrophy", "adrenomyeloneuropathy", "childhood cerebral ALD", "bronze Schilder disease", "ALD childhood cerebral form", "melanodermic leukodystrophy", "Siemerling-Creutzfeldt disease", "X-linked cerebral adrenoleukodystrophy", "Addison disease and cerebral sclerosis", "adrenoleukodystrophy X-linked cerebral form", "adrenoleukodystrophy childhood cerebral form", "childhood-onset cerebral X-linked adrenoleukodystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked cerebral adrenoleukodystrophy", "shortest_name_length": 3}
{"curie": "UMLS:C4721780", "names": ["Ovarian Cancer Stage IV", "Stage IV Ovarian Cancer", "Stage IV Ovarian Carcinoma", "FIGO Stage IV Ovarian Cancer", "AJCC Stage IV Ovarian Cancer", "FIGO Stage IV Cancer of Ovary", "Stage IV Ovarian Cancer AJCC v6", "Stage IV Ovarian Cancer AJCC v7", "FIGO Stage IV Ovarian Carcinoma", "FIGO Stage IV Carcinoma of Ovary", "FIGO Stage IV Cancer of the Ovary", "Stage IV Ovarian Epithelial Cancer", "stage IV ovarian epithelial cancer", "FIGO Stage IV Carcinoma of the Ovary", "Stage IV Ovarian Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Ovarian Cancer AJCC v6 and v7", "shortest_name_length": 23}
{"curie": "UMLS:C4721790", "names": ["Ovarian Cancer Stage IB", "Stage IB Ovarian Cancer", "AJCC Stage IB Ovarian Cancer", "FIGO Stage IB Ovarian Cancer", "FIGO Stage IB Cancer of Ovary", "Stage IB Ovarian Cancer AJCC v7", "Stage IB Ovarian Cancer AJCC v6", "FIGO Stage IB Ovarian Carcinoma", "FIGO Stage IB Carcinoma of Ovary", "FIGO Stage IB Cancer of the Ovary", "Stage IB Ovarian Epithelial Cancer", "FIGO Stage IB Carcinoma of the Ovary", "Stage IB Ovarian Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Ovarian Cancer AJCC v6 and v7", "shortest_name_length": 23}
{"curie": "UMLS:C2118574", "names": ["Corpus Callosum Neoplasm", "neoplasm of corpus callosum", "neoplasm of corpus callosum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplasm of corpus callosum", "shortest_name_length": 24}
{"curie": "MONDO:0006903", "names": ["Palsy peroneal", "peroneal palsy", "PALSY PERONEAL", "Peroneal Palsy", "Palsy, Peroneal", "Peroneal Palsies", "Paralysis peroneal", "PARALYSIS PERONEAL", "Peroneal nerve palsy", "peroneal nerve palsy", "PERONEAL NERVE PALSY", "nerve palsy peroneal", "nerve palsy, peroneal", "palsy, peroneal nerve", "n.peroneus; paralysis", "Peroneal Nerve Paralysis", "Peroneal Nerve Paralyses", "peroneal nerve paralysis", "Peroneal nerve paralysis", "paralysis; peroneal nerve", "Paralysis, Peroneal Nerve", "Nerve Paralysis, Peroneal", "Common peroneal nerve palsy", "common peroneal nerve palsy", "nerve palsy common peroneal", "lateral popliteal nerve palsy", "nerve palsy lateral popliteal", "Lateral popliteal nerve palsy", "Common peroneal nerve paralysis", "common peroneal nerve palsy (diagnosis)", "lateral popliteal nerve palsy (diagnosis)", "Common peroneal nerve paralysis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroneal nerve paralysis", "shortest_name_length": 14}
{"curie": "MONDO:0007200", "names": ["PASHAYAN SYNDROME", "Pashayan syndrome", "Pashayan-Prozansky syndrome", "Pashayan-Pruzansky syndrome", "blepharonasofacial syndrome", "Pashayan Prozansky syndrome", "blepharonasofacial malformation syndrome", "Blepharonasofacial malformation syndrome", "BLEPHARONASOFACIAL MALFORMATION SYNDROME", "Blepharonasofacial malformation syndrome (disorder)", "blepharonasofacial malformation syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blepharonasofacial malformation syndrome", "shortest_name_length": 17}
{"curie": "MONDO:0020657", "names": ["HPV-related squamous cell carcinoma", "HPV-Related Squamous Cell Carcinoma", "Squamous cell carcinoma, HPV-positive", "human papillomavirus-related squamous cell carcinoma", "Human Papillomavirus-Related Squamous Cell Carcinoma", "Human Papilloma Virus Related Squamous Cell Carcinoma", "human papilloma virus related squamous cell carcinoma", "human papilloma virus-related squamous cell carcinoma", "Human Papilloma Virus-Related Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "human papillomavirus-related squamous cell carcinoma", "shortest_name_length": 35}
{"curie": "MONDO:0018657", "names": ["CAPOK", "CAPOK SYNDROME", "CANCER, ALOPECIA, PIGMENT DYSCRASIA, ONYCHODYSTROPHY, AND KERATODERMA", "pigmentation defects-palmoplantar keratoderma-skin carcinoma syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pigmentation defects-palmoplantar keratoderma-skin carcinoma syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C2932678", "names": ["Inherited Peripheral Neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Inherited Peripheral Neuropathy", "shortest_name_length": 31}
{"curie": "MONDO:0016052", "names": ["PDD", "Atypical autism", "atypical autism", "atypical; autism", "autism; atypical", "Atypical autism (disorder)", "Atypical autistic syndrome", "atypical autism (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical autism", "shortest_name_length": 3}
{"curie": "UMLS:C1335053", "names": ["Non-Neoplastic Vascular Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Vascular Disorder", "shortest_name_length": 32}
{"curie": "MONDO:0060486", "names": ["AMC1", "AMCNMY", "arthrogryposis multiplex congenita-1", "arthrogryposis multiplex congenita, neurogenic, with myelin defect", "ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC, WITH MYELIN DEFECT", "ARTHROGRYPOSIS MULTIPLEX CONGENITA 1, NEUROGENIC, WITH MYELIN DEFECT", "arthrogryposis multiplex congenita 1, neurogenic, with myelin defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis multiplex congenita 1, neurogenic, with myelin defect", "shortest_name_length": 4}
{"curie": "UMLS:C0340613", "names": ["ARTERIAL ANEURYSM", "Arterial aneurysm", "arterial aneurysm", "aneurysm arterial", "Aneurysm;arterial", "aneurysms arterial", "aneurysm of artery", "Arterial aneurysms", "Arterial aneurysm NOS", "Arterial aneurysm (disorder)", "aneurysm of artery (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arterial aneurysm", "shortest_name_length": 17}
{"curie": "MONDO:0002658", "names": ["iris cancer", "cancer of iris", "tumor of the iris", "tumor of the Iris", "malignant iris tumor", "Malignant Iris Tumor", "Malignant Iris Neoplasm", "malignant tumor of iris", "Malignant tumor of iris", "Malignant Tumor of Iris", "malignant iris neoplasm", "Malignant tumour of iris", "Malignant neoplasm of iris", "malignant neoplasm of iris", "Malignant Neoplasm of Iris", "Malignant Tumor of the Iris", "malignant tumor of the iris", "malignant neoplasm of the iris", "malignant neoplasm of the Iris", "Malignant Neoplasm of the Iris", "Malignant tumor of iris (disorder)", "malignant neoplasm of iris (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "iris cancer", "shortest_name_length": 11}
{"curie": "MONDO:0011441", "names": ["RND", "RSDS", "CRPS1", "CRPS I", "Sudeck", "CRPS Type I", "CRPS Type Is", "Type I, CRPS", "Sudek Atrophy", "Algodystrophy", "Atrophy, Sudek", "Sudeks Atrophy", "atrophy; Sudeck", "Sudeck; atrophy", "sudek's atrophy", "Sudek's Atrophy", "Sudeck's Atrophy", "Sudeck's atrophy", "sudeck's atrophy", "Atrophy, Sudek's", "sudeck's syndrome", "Sudek's Atrophies", "Sudeck's syndrome", "Atrophies, Sudek's", "Reflex sympathetic dystrophy", "reflex sympathetic dystrophy", "REFLEX SYMPATHETIC DYSTROPHY", "Sudeck's atrophy (diagnosis)", "Reflex Sympathetic Dystrophy", "Dystrophy;reflex sympathetic", "Sympathetic Reflex Dystrophia", "Dystrophy, Reflex Sympathetic", "Sympathetic Dystrophy, Reflex", "reflex neurovascular dystrophy", "Sympathetic Reflex Dystrophias", "Reflex Sympathetic Dystrophies", "Reflex Neurovascular Dystrophy", "Reflex Dystrophia, Sympathetic", "Sympathetic Dystrophies, Reflex", "Dystrophies, Reflex Sympathetic", "Complex regional pain syndrome I", "Complex Regional Pain Syndrome I", "RSD - Reflex sympathetic dystrophy", "RSD (Reflex Sympathetic Dystrophy)", "RSDs (Reflex Sympathetic Dystrophy)", "complex regional pain syndrome type 1", "Complex regional pain syndrome Type I", "Type I Complex Regional Pain Syndrome", "REFLEX SYMPATHETIC DYSTROPHY SYNDROME", "Complex regional pain syndrome type 1", "Complex regional pain syndrome type I", "Reflex sympathetic dystrophy syndrome", "reflex sympathetic dystrophy syndrome", "Reflex Sympathetic Dystrophy Syndrome", "Pain Syndrome Type I, Complex Regional", "Syndrome, Reflex Sympathetic Dystrophy", "Complex Regional Pain Syndrome, Type I", "Pain Syndrome Type I, Regional, Complex", "Reflex sympathetic dystrophy, unspecified", "CRPS (complex regional pain syndrome) type I", "CRPS - Complex regional pain syndrome type I", "reflex sympathetic dystrophy syndrome (RSDS)", "Complex regional pain syndrome type I (disorder)", "Complex regional pain syndrome type I (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complex regional pain syndrome type 1", "shortest_name_length": 3}
{"curie": "MONDO:0010080", "names": ["FBSN", "SNDI", "familial IBSN", "striatal degeneration, familial", "familial bilateral striatal necrosis", "striatonigral degeneration, infantile", "infantile bilateral striatal necrosis", "bilateral striatal Necrosis, infantile", "familial infantile striatonigral necrosis", "familial infantile striatonigral degeneration", "familial infantile bilateral striatal necrosis", "hereditary infantile bilateral striatal necrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial infantile bilateral striatal necrosis", "shortest_name_length": 4}
{"curie": "MONDO:0100040", "names": ["FOXG1 disorder", "FOXG1 inherited genetic disease", "inherited genetic disease caused by mutation in FOXG1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FOXG1 disorder", "shortest_name_length": 14}
{"curie": "MONDO:0005011", "names": ["IBD1", "Crohn", "Crohn's", "crohn s", "crohns's", "eleocolitis", "Morbus Crohn", "Crohn Colitis", "disease crohn", "Crohn disease", "Crohn Disease", "CROHN DISEASE", "Disease Crohns", "Crohns disease", "crohns disease", "Crohns Disease", "Disease;Crohns", "DISEASE CROHNS", "crohn diseases", "disease crohn's", "CROHN'S DISEASE", "Crohn's disease", "crohn's disease", "Crohn's colitis", "Crohn's Colitis", "crohns diseases", "Crohn's Disease", "crohn s disease", "crohn's colitis", "crohn's diseases", "Regional colitis", "crohns's disease", "regional; colitis", "Crohn's Enteritis", "colitis; regional", "Crohn's enteritis", "enteritis regional", "Regional Enteritis", "regional enteritis", "REGIONAL ENTERITIS", "Regional enteritis", "colon crohn disease", "crohn disease colon", "Crohn's disease NOS", "Crohn's disease, NOS", "enteritis (regional)", "CC - Crohn's colitis", "CD - Crohn's disease", "crohn's disease colon", "GRANULOMATOUS COLITIS", "Crohns disease, colon", "crohn's colon disease", "granulomatous colitis", "Granulomatous Colitis", "Granulomatous colitis", "colon crohn's disease", "Crohn disease of colon", "regional enterocolitis", "Colitis, granulomatous", "Colitis, Granulomatous", "colitis; granulomatous", "large intestine; Crohn", "granulomatous; colitis", "Regional enterocolitis", "Crohn; large intestine", "colitis (granulomatous)", "Colonic Crohn's disease", "CROHNS DISEASE OF COLON", "Regional enteritis, NOS", "granulomatous enteritis", "Crohn's disease (colon)", "Crohn's disease of colon", "pediatric Crohn's disease", "Cicatrizing enterocolitis", "Pediatric Crohn's disease", "Crohn's disease (disorder)", "GC - Granulomatous colitis", "Crohn's disease (diagnosis)", "Granulomatous enteritis, NOS", "CROHN'S DISEASE OF THE COLON", "Crohn's disease, unspecified", "Inflammatory Bowel Disease 1", "Crohn disease of large bowel", "Crohn's disease of large bowel", "Crohn's (granulomatous) colitis", "Crohns disease, large intestine", "Granulomatous colitis (disorder)", "inflammatory bowel disease - IBD1", "Crohn's disease of large intestine", "Crohn's disease of colon (disorder)", "large intestine; regional enteritis", "regional enteritis; large intestine", "Granulomatous enteritis and colitis", "Regional enteritis (Crohn's disease)", "Crohn's disease [regional enteritis]", "Crohn's disease of colon (diagnosis)", "Regional enteritis of large intestine", "Regional enteritis of the large bowel", "Crohn's disease of large bowel (disorder)", "Crohn's (granulomatous) colitis (diagnosis)", "INFLAMMATORY BOWEL DISEASE (CROHN DISEASE) 1", "Crohn's disease [regional enteritis] of colon", "inflammatory bowel disease - IBD1 (diagnosis)", "Crohn's disease of large intestine (diagnosis)", "INFLAMMATORY BOWEL DISEASE, REGIONAL ENTERITIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Crohn disease", "shortest_name_length": 4}
{"curie": "UMLS:C0264290", "names": ["pharynx; cellulitis", "cellulitis; pharynx", "Pharyngeal Cellulitis", "Cellulitis of pharynx", "cellulitis of pharynx", "Cellulitis pharyngeal", "Pharyngeal cellulitis", "Cellulitis of pharynx (disorder)", "cellulitis of pharynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cellulitis of pharynx", "shortest_name_length": 19}
{"curie": "MONDO:0011890", "names": ["CMT1D", "HMSNID", "HMSN1D", "CMT 1D", "HMSN ID", "HMSN 1D", "Charcot-Marie-Tooth disease type 1D", "Charcot Marie Tooth disease type 1D", "Charcot-Marie-Tooth disease type ID", "Charcot-Marie-Tooth disease, type 1D", "CHARCOT-MARIE-TOOTH DISEASE, TYPE 1D", "Charcot-Marie-Tooth disease, Type 1D", "Charcot-Marie-Tooth neuropathy type 1D", "Charcot-Marie-Tooth neuropathy, type 1D", "Charcot-Marie-Tooth Neuropathy, Type 1D", "EGR2 Charcot-Marie-Tooth disease type 1", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 1D", "Hereditary motor and sensory neuropathy 1D", "HEREDITARY MOTOR AND SENSORY NEUROPATHY 1D", "hereditary motor and sensory neuropathy 1D", "Charcot-Marie-Tooth disease type ID (disorder)", "Charcot-Marie-Tooth disease type 1D (diagnosis)", "Charcot-Marie-Tooth disease, Type 1D (disorder)", "Charcot-Marie-Tooth disease, demyelinating, type 1D", "Charcot-Marie-Tooth disease, demyelinating, Type 1D", "CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1D", "Charcot-Marie-Tooth disease type 1 caused by mutation in EGR2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 1D", "shortest_name_length": 5}
{"curie": "MONDO:0030543", "names": ["COXPD54", "combined oxidative phosphorylation deficiency 54", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 54"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation deficiency 54", "shortest_name_length": 7}
{"curie": "MONDO:0002475", "names": ["Lacrimal Gland Adenocarcinoma", "lacrimal gland adenocarcinoma", "Adenocarcinoma of Lacrimal Gland", "adenocarcinoma of lacrimal gland", "Adenocarcinoma of lacrimal gland", "Adenocarcinoma of the Lacrimal Gland", "adenocarcinoma of the lacrimal gland", "Adenocarcinoma of lacrimal gland (disorder)", "adenocarcinoma of lacrimal gland (diagnosis)", "lacrimal gland neoplasm malignant adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lacrimal gland adenocarcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0002415", "names": ["bone carcinoma", "bone element carcinoma", "carcinoma of bone element"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bone carcinoma", "shortest_name_length": 14}
{"curie": "MONDO:0035940", "names": ["BCR-ABL1-like B-ALL", "B-ALL with BCR-ABL1", "B-ALL with t(9;22)(q34.1;q11.2)", "Philadelphia chromosome-like B-ALL", "B-lymphoblastic leukemia/lymphoma with BCR-ABL1", "B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)", "B-Lymphoblastic Leukemia/Lymphoma with t(9;22)(q34;q11.2); BCR-ABL1", "B Lymphoblastic Leukemia/Lymphoma with t(9;22)(q34;q11.2); BCR-ABL1", "B lymphoblastic leukemia/lymphoma with t(9;22)(q34;q11.2); BCR-ABL1", "B lymphoblastic leukemia lymphoma with t(9;22)(q34;q11.2); BCR-ABL1", "B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2);BCR-ABL1", "B lymphoblastic leukaemia lymphoma with t(9;22)(q34;q11.2); BCR-ABL1", "B Lymphoblastic Leukemia/Lymphoma with t(9;22)(q34.1;q11.2); BCR-ABL1", "B lymphoblastic leukemia lymphoma with t(9;22)(q34;q11.2); BCR-ABL1 (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)", "shortest_name_length": 19}
{"curie": "UMLS:C5419175", "names": ["COVID-19-Associated Thromboembolism", "SARS-CoV-2-Associated Thromboembolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "COVID-19-Associated Thromboembolism", "shortest_name_length": 35}
{"curie": "MONDO:0054763", "names": ["NBIA7", "NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 7", "neurodegeneration with brain iron accumulation 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodegeneration with brain iron accumulation 7", "shortest_name_length": 5}
{"curie": "MONDO:0014898", "names": ["PEOB3", "autosomal recessive progressive external ophthalmoplegia 3", "progressive external ophthalmoplegia, autosomal recessive 3", "PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE 3", "TK2 autosomal recessive progressive external ophthalmoplegia", "autosomal recessive progressive external ophthalmoplegia caused by mutation in TK2", "autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 3", "PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 3", "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3", "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive type 3", "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3; PEOB3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3", "shortest_name_length": 5}
{"curie": "MONDO:0008774", "names": ["AAKAD", "AMOXAD", "Ketoadipicaciduria", "2-KETOADIPIC ACIDURIA", "alpha-aminoadipic aciduria", "Alpha-aminoadipic aciduria", "2-aminoadipic 2-oxoadipic aciduria", "2-AMINOADIPIC 2-OXOADIPIC ACIDURIA", "2-aminoadipic 2-oxoadipic aciduria (disorder)", "ALPHA-AMINOADIPIC AND ALPHA-KETOADIPIC ACIDURIA", "alpha-aminoadipic and alpha-ketoadipic aciduria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "2-aminoadipic 2-oxoadipic aciduria", "shortest_name_length": 5}
{"curie": "MONDO:0006044", "names": ["renal sclerosis", "NEPHROSCLEROSIS", "Renal Sclerosis", "RENAL SCLEROSIS", "nephrosclerosis", "Nephrosclerosis", "Nephroscleroses", "Renal sclerosis", "sclerosis; renal", "kidney; sclerosis", "ARTERIOSCLEROSIS RENAL", "Arteriosclerosis renal", "renal arteriosclerosis", "Renal arteriosclerosis", "arteriosclerosis of kidney", "Arteriosclerosis of kidney", "Nephrosclerosis (disorder)", "Scarring of kidney arteries", "renal sclerosis (diagnosis)", "nephrosclerosis (diagnosis)", "Renal sclerosis, unspecified", "Thickening of kidney artiries", "Chronic arteriosclerotic nephritis", "Interstitial arteriosclerotic nephritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrosclerosis", "shortest_name_length": 15}
{"curie": "MONDO:0021935", "names": ["aspergillus niger infection", "Aspergillus niger infection", "infections, Aspergillus niger", "Infection by Aspergillus niger", "Infection caused by Aspergillus niger", "Aspergillus niger infection, pulmonary", "Infection caused by Aspergillus niger (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aspergillus niger infection", "shortest_name_length": 27}
{"curie": "MONDO:0022937", "names": ["deafness conductive stapedial ear malformation facial palsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness conductive stapedial ear malformation facial palsy", "shortest_name_length": 59}
{"curie": "MONDO:0003760", "names": ["ovarian germ cell tumor", "Ovarian Germ Cell Tumor", "Childhood Ovarian Germ Cell Tumor", "Pediatric Ovarian Germ Cell Tumor", "childhood ovarian germ cell tumor", "pediatric ovarian germ cell tumor", "paediatric ovarian germ cell tumour", "ovarian germ cell tumor of childhood", "pediatric ovarian germ cell neoplasm", "pediatric Ovarian germ cell neoplasm", "Childhood Ovarian Germ Cell Neoplasm", "childhood ovarian germ cell neoplasm", "Pediatric Ovarian Germ Cell Neoplasm", "paediatric Ovarian germ cell neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pediatric ovarian germ cell tumor", "shortest_name_length": 23}
{"curie": "UMLS:C5236063", "names": ["Advanced Pancreatic Ductal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Pancreatic Ductal Adenocarcinoma", "shortest_name_length": 41}
{"curie": "UMLS:C0206145", "names": ["Stunned myocardium", "stunned myocardium", "Stunned Myocardium", "myocardium stunning", "Myocardium, Stunned", "Stunned myocardium (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stunned Myocardium", "shortest_name_length": 18}
{"curie": "MONDO:0045013", "names": ["extraembryonic membrane disease", "disease of extraembryonic membrane", "disorder of extraembryonic membrane", "Disorder of extraembryonic membrane", "extraembryonic membrane disease or disorder", "Disorder of extraembryonic membrane (disorder)", "disease or disorder of extraembryonic membrane"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of extraembryonic membrane", "shortest_name_length": 31}
{"curie": "MONDO:0011145", "names": ["Coloboma-Obesity-Hypogenitalism-Mental Retardation Syndrome", "coloboma-obesity-hypogenitalism-mental retardation syndrome", "COLOBOMA-OBESITY-HYPOGENITALISM-MENTAL RETARDATION SYNDROME", "coloboma-obesity-hypogenitalism-intellectual disability syndrome", "colobomatous microphthalmia - obesity - hypogenitalism - intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colobomatous microphthalmia - obesity - hypogenitalism - intellectual disability syndrome", "shortest_name_length": 59}
{"curie": "MONDO:0003791", "names": ["prostatic urethral cancer", "Prostatic Urethral Malignant Neoplasm", "prostatic urethral malignant neoplasm", "prostatic urethra male urethral cancer", "male urethral cancer of prostatic urethra"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostatic urethral cancer", "shortest_name_length": 25}
{"curie": "UMLS:C1370879", "names": ["Recurrent Malignant Salivary Gland Neoplasm", "Malignant salivary gland neoplasm recurrent", "Recurrent Malignant Neoplasm of Salivary Gland", "Malignant neoplasm of salivary gland, unspecified, recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Malignant Neoplasm of Salivary Gland", "shortest_name_length": 43}
{"curie": "UMLS:C4553881", "names": ["Stage IVB Thyroid Gland Anaplastic Carcinoma AJCC v8", "Undifferentiated (Anaplastic) Stage IVB Thyroid Gland Cancer", "Stage IVB Thyroid Gland Undifferentiated (Anaplastic) Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Thyroid Gland Undifferentiated (Anaplastic) Carcinoma AJCC v8", "shortest_name_length": 52}
{"curie": "MONDO:0060641", "names": ["NEDSGA", "NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT SEIZURES AND GAIT ABNORMALITIES", "neurodevelopmental disorder with or without seizures and gait abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with or without seizures and gait abnormalities", "shortest_name_length": 6}
{"curie": "MONDO:0003616", "names": ["Adenosalpingitis", "Adenosis, fallopian tube", "Adenosis of fallopian tube", "Salpingitis isthmica nodosa", "Salpingitis Isthmica Nodosa", "SALPINGITIS ISTHMICA NODOSA", "salpingitis isthmica nodosa", "isthmica nodosa salpingitis", "Salpingitis isthmica nodosa (disorder)", "salpingitis isthmica nodosa (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "salpingitis isthmica nodosa", "shortest_name_length": 16}
{"curie": "MONDO:0010002", "names": ["RTS", "Rothmund", "Congenital Poikiloderma", "Congenital poikiloderma", "congenital poikiloderma", "Poikiloderma congenitale", "Poikiloderma, congenital", "Poikiloderma Congenitale", "congenital; poikiloderma", "poikiloderma; congenital", "poikiloderma congenitale", "rothmund-thomson syndrome", "Poikiloderma Congenitales", "Rothmund-Thomson syndrome", "Rothmund-Thomson Syndrome", "ROTHMUND-THOMSON SYNDROME", "Congenitale, Poikiloderma", "Rothmund Thomson Syndrome", "rothmund thomson syndrome", "Syndrome, Rothmund-Thomson", "Congenitales, Poikiloderma", "Rothmund-Thompson Syndrome", "Rothmund-Thomson Poikiloderma", "Rothmund-Thomson Poikilodermas", "Poikiloderma of Rothmund Thomson", "Poikiloderma of Rothmund-Thomson", "poikiloderma of Rothmund-Thomson", "Poikiloderma congenitale syndrome", "congenital poikiloderma (diagnosis)", "Rothmund-Thomson syndrome (disorder)", "poikiloderma atrophicans and cataract", "POIKILODERMA ATROPHICANS AND CATARACT", "Poikiloderma Atrophicans and Cataract", "Poikiloderma congenitale of Rothmund-Thomson", "Poikiloderma Congenitale of Rothmund-Thomson"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rothmund-Thomson syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C5554608", "names": ["Metastatic Malignant Nongerminomatous Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Malignant Nongerminomatous Germ Cell Tumor", "shortest_name_length": 53}
{"curie": "UMLS:C0948389", "names": ["bowel; hypomotility", "hypomotility; bowel", "Intestinal hypomotility"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal hypomotility", "shortest_name_length": 19}
{"curie": "MONDO:0100108", "names": ["TPM3 myopathy", "TPM3-related myopathy", "congenital myopathy related to TPM3", "autosomal dominant TPM3-related myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "TPM3-related myopathy", "shortest_name_length": 13}
{"curie": "MONDO:0017962", "names": ["46,XX DSD induced by fetoplacental androgens excess", "46,XX disorder of sex development induced by fetoplacental androgens excess"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XX disorder of sex development induced by fetoplacental androgens excess", "shortest_name_length": 51}
{"curie": "MONDO:0011883", "names": ["CHACS", "Chacs", "Chac syndrome", "CHAC syndrome", "CURLY HAIR-ACRAL KERATODERMA-CARIES SYNDROME", "Curly hair-acral keratoderma-caries syndrome", "Curly hair, acral keratoderma, caries syndrome", "Curly hair - acral keratoderma - caries syndrome", "CHACS - curly hair, acral keratoderma, caries syndrome", "Curly hair, acral keratoderma, caries syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Curly hair - acral keratoderma - caries syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0005997", "names": ["TS", "ts", "TRICUSPID STENOSIS", "tricuspid stenosis", "Tricuspid Stenosis", "Tricuspid stenosis", "stenosis; tricuspid", "TS - Tricuspid stenosis", "TRICUSPID VALVE STENOSIS", "Tricuspid Valve Stenoses", "tricuspid valve stenosis", "Tricuspid valve stenosis", "Tricuspid Valve Stenosis", "TRICUSPID VALVE, STENOSIS", "Valve Stenoses, Tricuspid", "Stenosis, Tricuspid Valve", "Stenoses, Tricuspid Valve", "Valve Stenosis, Tricuspid", "tricuspid (valve); stenosis", "tricuspid (valve); stricture", "Tricuspid valve stenosis, NOS", "tricuspid stenosis (diagnosis)", "Tricuspid valve stenosis (disorder)", "narrowing of the heart's tricuspid valve"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tricuspid valve stenosis", "shortest_name_length": 2}
{"curie": "UMLS:C1336379", "names": ["Stage IVB Nasopharynx Carcinoma", "Stage IVB Carcinoma of Nasopharynx", "Stage IVB Nasopharyngeal Carcinoma", "Stage IVB Nasopharyngeal Throat Cancer", "Stage IVB Carcinoma of the Nasopharynx", "Stage IVB Nasopharyngeal Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Nasopharyngeal Carcinoma AJCC v7", "shortest_name_length": 31}
{"curie": "UMLS:C5555845", "names": ["Metastatic Carcinoma in the Peritoneum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Carcinoma in the Peritoneum", "shortest_name_length": 38}
{"curie": "MONDO:0011170", "names": ["LGMD2G", "LGMDR7", "LGMD type 2G", "Telethonin-related LGMD R7", "LGMD due to telethonin deficiency", "Limb-girdle muscular dystrophy type 2G", "muscular dystrophy, limb-girdle type 2G", "limb-girdle muscular dystrophy, type 2G", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2G", "Muscular Dystrophy, Limb-Girdle, Type 2G", "muscular dystrophy, limb-girdle, type 2G", "muscular dystrophy, limb-girdle type 2G (diagnosis)", "Telethonin-related limb-girdle muscular dystrophy R7", "progressive muscular dystrophy - limb girdle - type 2g", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 7", "muscular dystrophy, limb-girdle, autosomal recessive 7", "Tcap autosomal recessive limb-girdle muscular dystrophy", "TCAP autosomal recessive limb-girdle muscular dystrophy", "Autosomal recessive limb girdle muscular dystrophy type 2G", "Autosomal recessive limb-girdle muscular dystrophy type 2G", "autosomal recessive limb-girdle muscular dystrophy type 2G", "Limb-girdle muscular dystrophy due to telethonin deficiency", "limb-girdle muscular dystrophy due to telethonin deficiency", "Limb girdle muscular dystrophy due to telethonin deficiency", "Autosomal recessive limb girdle muscular dystrophy type 2G (disorder)", "autosomal recessive limb-girdle muscular dystrophy caused by mutation in TCAP", "autosomal recessive limb-girdle muscular dystrophy caused by mutation in Tcap"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive limb-girdle muscular dystrophy type 2G", "shortest_name_length": 6}
{"curie": "MONDO:0006039", "names": ["Septic colitis", "septic colitis", "colitis; septic", "septic; colitis", "infective colitis", "Infective colitis", "Infectious Colitis", "infectious colitis", "COLITIS INFECTIOUS", "Infectious colitis", "Colitis;infectious", "colitis; infectious", "infectious; colitis", "Septic colitis, NOS", "Infectious colitis NOS", "Infectious colitis, NOS", "septic colitis (diagnosis)", "Infectious colitis (disorder)", "infectious colitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infectious colitis", "shortest_name_length": 14}
{"curie": "MONDO:0001312", "names": ["Acute serous otitis media", "Otitis media serous acute", "acute serous otitis media", "otitis; media, acute, serous", "otitis; media, serous, acute", "Otitis media serous acute NOS", "acute serous otitis media (diagnosis)", "Acute nonsuppurative serous otitis media", "Acute non-suppurative serous otitis media", "Acute serous otitis media, unspecified ear", "Acute non-suppurative otitis media - serous", "acute non-suppurative otitis media - serous", "Acute non-suppurative serous otitis media (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute serous otitis media", "shortest_name_length": 25}
{"curie": "UMLS:C1997728", "names": ["osteomyelitis due to staphylococcus aureus", "Osteomyelitis due to Staphylococcus aureus", "Osteomyelitis caused by Staphylococcus aureus", "osteomyelitis due to staphylococcus aureus (diagnosis)", "Osteomyelitis caused by Staphylococcus aureus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Osteomyelitis due to Staphylococcus aureus", "shortest_name_length": 42}
{"curie": "MONDO:0003955", "names": ["Swiss cheese disease", "Swiss Cheese Disease", "breast juvenile papillomatosis", "Juvenile Breast Papillomatosis", "juvenile breast papillomatosis", "Juvenile papillomatosis of breast", "juvenile papillomatosis of breast", "Juvenile Papillomatosis of Breast", "Juvenile papillomatosis of the breast", "Juvenile Papillomatosis of the Breast", "juvenile papillomatosis of the breast", "Juvenile papillomatosis of breast (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile breast papillomatosis", "shortest_name_length": 20}
{"curie": "MONDO:0010652", "names": ["Tranebjaerg-Svejgaard syndrome", "Tranebjaerg Svejgaard syndrome", "mental retardation and psoriasis", "MENTAL RETARDATION AND PSORIASIS", "intellectual disability and psoriasis", "Mental Retardation associated with Psoriasis", "X-linked mental retardation associated with psoriasis", "X-linked intellectual disability - seizures - psoriasis", "X-linked intellectual disability associated with psoriasis", "X-linked intellectual disability-seizures-psoriasis syndrome", "X-linked intellectual disability with seizure and psoriasis syndrome", "Mental retardation X-linked, Tranebjaerg type seizures and psoriasis", "mental retardation X-linked, Tranebjaerg type seizures and psoriasis", "x-linked intellectual disability with seizure and psoriasis syndrome", "intellectual disability X-linked, Tranebjaerg type seizures and psoriasis", "X-linked intellectual disability with seizure and psoriasis syndrome (disorder)", "x-linked intellectual disability with seizure and psoriasis syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability-seizures-psoriasis syndrome", "shortest_name_length": 30}
{"curie": "MONDO:0003047", "names": ["thymic LCNEC", "Thymic LCNEC", "Thymus large cell carcinoma", "thymus large cell carcinoma", "large cell carcinoma of the Thymus", "thymus large cell neuroendocrine carcinoma", "Thymic Large Cell Neuroendocrine Carcinoma", "thymic large cell neuroendocrine carcinoma", "large cell neuroendocrine carcinoma of thymus", "Large Cell Neuroendocrine Carcinoma of Thymus", "large cell neuroendocrine carcinoma of Thymus", "Large Cell Neuroendocrine Carcinoma of the Thymus", "large cell neuroendocrine carcinoma of the Thymus", "large cell neuroendocrine carcinoma of thymus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thymic large cell neuroendocrine carcinoma", "shortest_name_length": 12}
{"curie": "UMLS:C1701940", "names": ["Ventilator-acquired pneumonia", "Ventilator-Associated Pneumonia", "Ventilator-associated pneumonia", "Ventilator associated pneumonia", "ventilator-associated pneumonia", "Pneumonia, Ventilator-Associated", "ventilator associated pneumonitis", "pneumonitis ventilator associated", "Ventilator associated pneumonitis", "ventilator-associated pneumonia (VAP)", "VAP - ventilator associated pneumonia", "Ventilator-acquired pneumonia (disorder)", "ventilator-associated pneumonia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pneumonia, Ventilator-Associated", "shortest_name_length": 29}
{"curie": "MONDO:0018746", "names": ["Ocular pemphigus", "ocular pemphigus", "ocular pemphigoid", "PEMPHIGUS, OCULAR", "Ocular pemphigoid", "mucosal pemphigoid", "cicatricial pemphigoid", "Mucosynechial pemphigoid", "benign mucosal pemphigoid", "mucous membrane pemphigoid", "Ocular pemphigoid (diagnosis)", "conjunctiva ocular pemphigoid", "benign mucous membrane pemphigoid", "Benign Mucous Membrane Pemphigoid", "benign mucous Membrane pemphigoid", "benign mucous membrance pemphigoid", "cicatricial pemphigoid with ocular involvement", "Cicatricial pemphigoid with ocular involvement", "Benign mucous membrane pemphigoid with ocular involvement", "benign mucous membrane pemphigoid with ocular involvement", "cicatricial pemphigoid with ocular involvement (diagnosis)", "Benign mucous membrane pemphigoid with ocular involvement (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucous membrane pemphigoid", "shortest_name_length": 16}
{"curie": "UMLS:C1336140", "names": ["Stage IB Osteosarcoma", "Stage IB Osteogenic Sarcoma", "Stage IB Osteosarcoma AJCC v7", "Stage IB Osteosarcoma  AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Osteosarcoma AJCC v7", "shortest_name_length": 21}
{"curie": "MONDO:0024565", "names": ["EDSS", "EDSS1", "Ectodermal dysplasia-syndactyly syndrome", "ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1", "ectodermal dysplasia-syndactyly syndrome 1", "NECTIN4 ectodermal dysplasia-syndactyly syndrome", "ectodermal dysplasia-syndactyly syndrome caused by mutation in NECTIN4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia-syndactyly syndrome 1", "shortest_name_length": 4}
{"curie": "MONDO:0033862", "names": ["primary autoimmune enteropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary autoimmune enteropathy", "shortest_name_length": 30}
{"curie": "MONDO:0003858", "names": ["anterior optic tract meningioma", "Anterior Visual Pathway Meningioma", "anterior visual pathway meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anterior optic tract meningioma", "shortest_name_length": 31}
{"curie": "MONDO:0044070", "names": ["Candidemia", "candidemia", "Candidaemia", "Candidemias", "candidaemia", "Candidemia (disorder)", "candidemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "candidemia", "shortest_name_length": 10}
{"curie": "UMLS:C1336001", "names": ["Small Bowel Lipoma", "Lipoma of Small Bowel", "Small Intestinal Lipoma", "lipoma of small intestine", "Lipoma of the Small Bowel", "Lipoma of Small Intestine", "Lipoma of small intestine", "Lipoma of the Small Intestine", "Lipoma of small intestine (disorder)", "lipoma of small intestine (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lipoma of small intestine", "shortest_name_length": 18}
{"curie": "MONDO:0005847", "names": ["Brock", "Brock Syndrome", "brock syndrome", "BROCK SYNDROME", "Brock syndrome", "Brocks Syndrome", "brocks syndrome", "brock's syndrome", "Brock's syndrome", "Brock's Syndrome", "Syndrome, Brock's", "middle lobe syndrome", "Middle lobe syndrome", "Middle Lobe Syndrome", "syndrome; middle lobe", "middle lobe; syndrome", "Syndromes, Middle Lobe", "lung middle lobe syndrome", "LUNG, MIDDLE LOBE SYNDROME", "lobe lungs middle syndrome", "Middle lobe syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "middle lobe syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C1334059", "names": ["HPV-Related Vulvar Squamous Cell Carcinoma", "Human Papillomavirus-Related Vulvar Squamous Cell Carcinoma", "Human Papilloma Virus Related Vulvar Squamous Cell Carcinoma", "Human Papilloma Virus-Related Vulvar Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Human Papillomavirus-Related Vulvar Squamous Cell Carcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0015994", "names": ["Atrophie blanche", "muscular dystrophy white matter spongiosis", "muscular dystrophy-white matter spongiosis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy-white matter spongiosis syndrome", "shortest_name_length": 16}
{"curie": "UMLS:C0339483", "names": ["radiation retinopathy", "Radiation retinopathy", "Radiation Retinopathy", "Radiation retinopathy (disorder)", "radiation retinopathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radiation retinopathy", "shortest_name_length": 21}
{"curie": "UMLS:C4521756", "names": ["0", "Stage 0 Gastric (Stomach) Cancer", "Pathologic Stage 0 Gastric Cancer AJCC v8", "Pathologic Stage 0 Gastric Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage 0 Gastric Cancer AJCC v8", "shortest_name_length": 1}
{"curie": "MONDO:0000351", "names": ["Methioninemia", "methioninemia", "MAT Deficiency", "MAT DEFICIENCY", "MAT deficiency", "Hypermethioninemia", "hypermethioninemia", "Hypermethioninaemia", "hypermethioninaemia", "MAT I/III Deficiency", "MAT I/III DEFICIENCY", "MAT I/III deficiency", "Hypermethioninemia, NOS", "Increased methionine in blood", "Hypermethioninemia (disorder)", "hypermethioninemia (diagnosis)", "disorder of methionine catabolism", "Isolated Persistent Hypermethioninemia", "HYPERMETHIONINEMIA, ISOLATED PERSISTENT", "Hypermethioninemia, Isolated Persistent", "Methionine Adenosyltransferase Deficiency", "Methionine adenosyltransferase deficiency", "inborn methionine catabolic process disorder", "inborn error of methionine catabolic process", "Deficiency of Methionine Adenosyltransferase", "Deficiency of methionine adenosyltransferase", "METHIONINE ADENOSYLTRANSFERASE I/III DEFICIENCY", "rare inborn error of methionine catabolic process", "Hepatic methionine adenosyltransferase deficiency", "Hepatic Methionine Adenosyltransferase Deficiency", "Deficiency of methionine adenosyltransferase (disorder)", "Hepatic methionine adenosyltransferase deficiency (disorder)", "Brain demyelination due to methionine adenosyltransferase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of methionine catabolism", "shortest_name_length": 13}
{"curie": "UMLS:C0746087", "names": ["Small cell lung cancer metastatic", "LUNG CANCER SMALL CELL METASTATIC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small cell lung cancer metastatic", "shortest_name_length": 33}
{"curie": "MONDO:0018318", "names": ["disorder of asparagine metabolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of asparagine metabolism", "shortest_name_length": 33}
{"curie": "UMLS:C5206342", "names": ["Unresectable Rectal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Rectal Adenocarcinoma", "shortest_name_length": 34}
{"curie": "UMLS:C4682582", "names": ["Stage II Uterine Corpus Adenosarcoma", "Stage II Uterine Corpus Adenosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Uterine Corpus Adenosarcoma AJCC v8", "shortest_name_length": 36}
{"curie": "MONDO:0001518", "names": ["Spastic entropion", "spastic entropion", "Spastic entropion (disorder)", "spastic entropion (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic entropion", "shortest_name_length": 17}
{"curie": "UMLS:C0334526", "names": ["Strumal Carcinoid", "Strumal carcinoid", "strumal; carcinoid", "carcinoid; strumal", "struma ovarii; carcinoid", "Struma Ovarii and Carcinoid", "Struma ovarii and carcinoid", "carcinoid; with struma ovarii", "struma; ovarii, with carcinoid", "Strumal carcinoid (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Strumal carcinoid", "shortest_name_length": 17}
{"curie": "MONDO:0016163", "names": ["SCA7", "ADCA2", "OPCA3", "OPCA 3", "ADCAII", "OPCA III", "Adca, type 2", "ADCA, TYPE II", "ADCA, type II", "Spinocerebellar Ataxia 7", "spinocerebellar ataxia 7", "SPINOCEREBELLAR ATAXIA 7", "Spinocerebellar Ataxia-7", "spinocerebellar ataxia-7", "Spinocerebellar Ataxia 7s", "Ataxia 7, Spinocerebellar", "spinocerebellar ataxia type 7", "Spinocerebellar Ataxia Type 7", "Type 7 Spinocerebellar Ataxia", "Spinocerebellar ataxia type 7", "olivopontocerebellar atrophy 3", "OPCA with Retinal Degeneration", "OPCA WITH RETINAL DEGENERATION", "OPCA with retinal Degeneration", "Olivopontocerebellar Atrophy III", "OLIVOPONTOCEREBELLAR ATROPHY III", "Olivopontocerebellar Atrophy IIIs", "Atrophy III, Olivopontocerebellar", "Ataxia with pigmentary retinopathy", "ataxia with pigmentary retinopathy", "Spinocerebellar ataxia type 7 (disorder)", "Cerebellar syndrome pigmentary maculopathy", "Autosomal dominant cerebellar ataxia type 2", "autosomal dominant cerebellar ataxia type 2", "autosomal dominant cerebellar ataxia, type 2", "autosomal dominant cerebellar ataxia type II", "Autosomal dominant cerebellar ataxia type II", "Autosomal Dominant Cerebellar Ataxia, Type II", "AUTOSOMAL DOMINANT CEREBELLAR ATAXIA, TYPE II", "ATXN7 autosomal dominant cerebellar ataxia type II", "cerebellar syndrome-pigmentary maculopathy syndrome", "Cerebellar syndrome-pigmentary maculopathy syndrome", "Autosomal dominant cerebellar ataxia type 2 (disorder)", "OPCA WITH MACULAR DEGENERATION AND EXTERNAL OPHTHALMOPLEGIA", "OPCA with Macular Degeneration and External Ophthalmoplegia", "OPCA with macular Degeneration and external ophthalmoplegia", "autosomal dominant cerebellar ataxia type II caused by mutation in ATXN7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant cerebellar ataxia type II", "shortest_name_length": 4}
{"curie": "MONDO:0060671", "names": ["EJM10", "juvenile myoclonic epilepsy 10", "epilepsy, juvenile myoclonic, susceptibility to, 10", "EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, juvenile myoclonic, susceptibility to, 10", "shortest_name_length": 5}
{"curie": "MONDO:0022642", "names": ["carcinoid tumor childhood", "Childhood Carcinoid Tumor", "childhood carcinoid tumor", "Childhood Neuroendocrine Tumor G1", "pediatric carcinoid tumor (disease)", "childhood carcinoid tumor (disease)", "carcinoid tumor (disease) of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood carcinoid tumor", "shortest_name_length": 25}
{"curie": "UMLS:C0809983", "names": ["Schizophrenia and related disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Schizophrenia and related disorders", "shortest_name_length": 35}
{"curie": "MONDO:0016890", "names": ["monosomy 8p", "deletion 8p", "8p deletion", "8p monosomy", "partial monosomy 8p", "8p- syndrome (partial)", "chromosome 8p deletion", "8p deletion syndrome (partial)", "partial monosomy of chromosome 8p", "partial deletion of chromosome 8p", "Chromosome 8p deletion syndrome (partial)", "partial deletion of the short arm of chromosome 8", "partial monosomy of the short arm of chromosome 8", "partial deletion of the short arm of chromosome type 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of the short arm of chromosome 8", "shortest_name_length": 11}
{"curie": "MONDO:0016942", "names": ["partial trisomy/tetrasomy of chromosome 5p", "partial duplication/triplication of chromosome 5p", "partial trisomy/tetrasomy of the short arm of chromosome 5", "partial trisomy/tetrasomy of the short arm of chromosome type 5", "partial duplication/triplication of the short arm of chromosome 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial trisomy/tetrasomy of the short arm of chromosome 5", "shortest_name_length": 42}
{"curie": "MONDO:0004979", "names": ["asthma", "Asthma", "obsolete_asthma", "Exertional asthma", "asthma induced exercise", "Exercise Induced Asthma", "Exercise induced asthma", "exercise induced asthma", "Exercise-induced asthma", "Asthma exercise induced", "Exercise-Induced Asthma", "asthma exercise induced", "exercise-induced asthma", "ASTHMA EXERCISED INDUCED", "exercised induced asthma", "Asthma, Exercise-Induced", "Exercise-Induced Asthmas", "Asthma, Exercise Induced", "bronchial hyperreactivity", "chronic obstructive asthma", "EIA - Exercise-induced asthma", "EIA (exercise-induced asthma)", "Exercise-induced asthma (disorder)", "exercise-induced asthma (diagnosis)", "chronic obstructive asthma with status asthmaticus", "chronic obstructive asthma with acute exacerbation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "asthma", "shortest_name_length": 6}
{"curie": "UMLS:C2348517", "names": ["Favorable Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Favorable Hodgkin Lymphoma", "shortest_name_length": 26}
{"curie": "UMLS:C0342494", "names": ["Hyperplasia adrenal cortex", "Adrenal Cortex Hyperplasia", "Adrenal cortex hyperplasia", "ADRENAL CORTEX HYPERPLASIA", "HYPERPLASIA ADRENAL CORTEX", "Adrenocortical Hyperplasia", "Adrenocortical hyperplasia", "Adrenal Cortical Hyperplasia", "Hyperplasia of Adrenal Cortex", "Hyperplasia of the Adrenal Cortex", "Adrenocortical hyperplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adrenocortical hyperplasia", "shortest_name_length": 26}
{"curie": "UMLS:C0751914", "names": ["Adult Pelizaeus Merzbacher Disease", "Adult Pelizaeus-Merzbacher Disease", "Pelizaeus Merzbacher Disease, Adult", "Pelizaeus-Merzbacher Disease, Adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Pelizaeus-Merzbacher Disease", "shortest_name_length": 34}
{"curie": "UMLS:C0854571", "names": ["Reocclusion", "reocclusion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reocclusion", "shortest_name_length": 11}
{"curie": "MONDO:0017379", "names": ["Lundberg syndrome", "polyneuropathy mental retardation acromicria premature menopause", "polyneuropathy intellectual disability acromicria premature menopause", "polyneuropathy - intellectual deficit - acromicria - premature menopause", "polyneuropathy-intellectual disability-acromicria-premature menopause syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyneuropathy-intellectual disability-acromicria-premature menopause syndrome", "shortest_name_length": 17}
{"curie": "MONDO:0004008", "names": ["FEA", "DIN 1A", "Clinging Carcinoma", "clinging carcinoma", "Flat Epithelial Atypia", "flat epithelial atypia", "flat ductal epithelial atypia", "Flat Ductal Epithelial Atypia", "Flat epithelial atypia of breast", "Flat Epithelial Atypia of the Breast", "Breast Flat Ductal Epithelial Atypia", "flat epithelial atypia of the breast", "ductal intraepithelial neoplasia, grade 1A", "Ductal Intraepithelial Neoplasia, Grade 1A", "flat ductal epithelial atypia of the breast", "Flat Ductal Epithelial Atypia of the Breast", "Flat epithelial atypia of breast (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "flat ductal epithelial atypia", "shortest_name_length": 3}
{"curie": "MONDO:0007947", "names": ["MFS", "MFS1", "Marfan", "MARFAN SYNDROME", "Marfan Syndrome", "Marfan syndrome", "marfan syndrome", "marfan's disease", "Marfans Syndrome", "Marfan's disease", "Marfans syndrome", "marfans syndrome", "marfan's syndrome", "Marfan's syndrome", "MARFAN'S SYNDROME", "Marfan's Syndrome", "Marfan syndrome type 1", "Marfan Syndrome Type 1", "MARFAN SYNDROME, TYPE I", "Marfan syndrome, type 1", "Marfan Syndrome, Type I", "Marfan syndrome (diagnosis)", "Marfan's syndrome (disorder)", "Marfan's syndrome, unspecified", "Marfan syndrome type 1 (disorder)", "Marfan syndrome type 1 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Marfan syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0008970", "names": ["BLC", "BOCD", "Blomstrand syndrome", "Blomstrand chondrodysplasia", "chondrodysplasia Blomstrand type", "Blomstrand type chondrodysplasia", "Blomstrand Type Chondrodysplasia", "Blomstrand osteochondrodysplasia", "CHONDRODYSPLASIA, BLOMSTRAND TYPE", "Chondrodysplasia, blomstrand type", "Chondrodysplasia, Blomstrand type", "chondrodysplasia, Blomstrand type", "Blomstrand lethal chondrodysplasia", "Blomstrand's lethal chondrodysplasia", "Blomstrand lethal osteochondrodysplasia", "Lethal congenital dwarfism with accelerated skeletal maturation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chondrodysplasia Blomstrand type", "shortest_name_length": 3}
{"curie": "MONDO:0013778", "names": ["PHA2C", "Pseudohypoaldosteronism type 2C", "pseudohypoaldosteronism type 2C", "pseudohypoaldosteronism, type 2C", "pseudohypoaldosteronism, type IIC", "PSEUDOHYPOALDOSTERONISM, TYPE IIC", "Pseudohypoaldosteronism, Type IIc", "WNK1 pseudohypoaldosteronism type 2", "pseudohypoaldosteronism type 2 caused by mutation in WNK1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudohypoaldosteronism type 2C", "shortest_name_length": 5}
{"curie": "UMLS:C4525091", "names": ["Stage IIIA Colorectal Cancer AJCC v8", "Stage IIIA Colorectal Carcinoma AJCC v8", "Stage IIIA Colorectal (Colon or Rectal) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Colorectal Cancer AJCC v8", "shortest_name_length": 36}
{"curie": "MONDO:0014941", "names": ["DAIPT", "ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH", "arthrogryposis, distal, with impaired proprioception and touch", "arthrogryposis, distal, with impaired proprioception and touch; DAIPT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis, distal, with impaired proprioception and touch", "shortest_name_length": 5}
{"curie": "MONDO:0002411", "names": ["narcissistic personality", "Narcissistic personality", "narcissistic personalities", "narcissistic personality disorder", "Narcissistic Personality Disorder", "PERSONALITY DISORDER NARCISSISTIC", "Narcissistic personality disorder", "personality disorder; narcissistic", "narcissistic; personality disorder", "Personality Disorder, Narcissistic", "Narcissistic personality disorder (disorder)", "narcissistic personality disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "narcissistic personality disorder", "shortest_name_length": 24}
{"curie": "MONDO:0030902", "names": ["MC1DN36", "mitochondrial complex I deficiency, nuclear type 36", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 36", "mitochondrial complex 1 deficiency, nuclear type 36"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 36", "shortest_name_length": 7}
{"curie": "UMLS:C0677967", "names": ["Prostate Cancer by Jewett Stage", "Prostate Cancer by Whitmore Stage", "Prostate Cancer by Whitmore-Jewett Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Cancer by Whitmore-Jewett Stage", "shortest_name_length": 31}
{"curie": "UMLS:C4087051", "names": ["MENINGOHYDROENCEPHALOCELE", "Meningohydroencephalocele"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meningohydroencephalocele", "shortest_name_length": 25}
{"curie": "MONDO:0015314", "names": ["Primary laryngeal lymphangioma", "primary laryngeal lymphangioma", "Congenital lymphangioma of larynx", "Congenital lymphangioma of larynx (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary laryngeal lymphangioma", "shortest_name_length": 30}
{"curie": "MONDO:0003298", "names": ["Vulvar Leiomyoma", "vulvar leiomyoma", "mammalian vulva leiomyoma", "leiomyoma of mammalian vulva"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar leiomyoma", "shortest_name_length": 16}
{"curie": "MONDO:0011941", "names": ["MTBS1", "tuberculosis, susceptibility to", "MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, 1", "mycobacterium tuberculosis, susceptibility to, 1", "Mycobacterium tuberculosis, susceptibility to, type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mycobacterium tuberculosis, susceptibility to, 1", "shortest_name_length": 5}
{"curie": "UMLS:C1708716", "names": ["Pericardial Fibroma", "Pericardial Benign Mesothelioma", "Pericardial Fibrous Mesothelioma", "Pericardial Solitary Fibrous Tumor", "Pericardial Submesothelial Fibroma", "Benign Pericardial Mesothelial Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pericardial Solitary Fibrous Tumor", "shortest_name_length": 19}
{"curie": "MONDO:0022884", "names": ["Van Biervliet Hendrickx Van Ertbruggen syndrome", "craniofacial dysostosis arthrogryposis progeroid appearence"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniofacial dysostosis arthrogryposis progeroid appearence", "shortest_name_length": 47}
{"curie": "MONDO:0009463", "names": ["Small internal carotid artery", "Internal carotid artery hypoplasia", "Aplasia of internal carotid artery", "Hypotrophic internal carotid artery", "Deficiency of internal carotid artery", "INTERNAL CAROTID ARTERIES, HYPOPLASIA OF", "internal carotid arteries, hypoplasia of", "Decreased size of internal carotid artery"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "internal carotid arteries, hypoplasia of", "shortest_name_length": 29}
{"curie": "MONDO:0003829", "names": ["Renal Papillary Adenoma", "Renal papillary adenoma", "renal papillary adenoma", "Papillary adenoma of kidney", "Papillary Adenoma of the Kidney", "Papillary adenoma of the kidney", "papillary adenoma of the kidney", "Chromophil Adenoma of the Kidney", "chromophil adenoma of the kidney", "Renal papillary adenoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromophil adenoma of the kidney", "shortest_name_length": 23}
{"curie": "MONDO:0006018", "names": ["Wissler Syndrome", "Wissler syndrome", "Wisslers Syndrome", "Wissler's Syndrome", "Wissler's syndrome", "Syndrome, Wissler's", "Subsepsis Allergica", "Subsepsis hyperergia", "Subsepsis Hyperergica", "Wissler-Fanconi syndrome", "Wissler Fanconi Syndrome", "Wissler-Fanconi Syndrome", "Syndrome, Wissler-Fanconi", "Wissler's subsepsis allergica", "Subsepsis hyperergia syndrome", "Wissler-Fanconi syndrome (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wissler syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0009944", "names": ["pyloric atresia", "Pyloric Atresia", "PYLORIC ATRESIA", "Pyloric atresia", "Pyloric atresia (disorder)", "Pyloric atresia (diagnosis)", "anomalies of stomach pyloric atresia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyloric atresia", "shortest_name_length": 15}
{"curie": "MONDO:0017423", "names": ["split hand or/and split foot malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "split hand or/and split foot malformation", "shortest_name_length": 41}
{"curie": "MONDO:0017503", "names": ["Bilateral acheiria", "acheiria, bilateral", "Bilateral agenesis of hands", "Bilateral acheiria (disorder)", "congenital absence of hand, bilateral", "Bilateral congenital absence of hands"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acheiria, bilateral", "shortest_name_length": 18}
{"curie": "MONDO:0002509", "names": ["granulomatous orchitis", "Granulomatous orchitis", "Non-Specific Granulomatous Orchitis", "non-specific granulomatous orchitis", "Non-specific granulomatous orchitis", "Non-specific granulomatous orchitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-specific granulomatous orchitis", "shortest_name_length": 22}
{"curie": "MONDO:0032894", "names": ["NEDESBA", "neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy", "NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, SPASTICITY, AND BRAIN ATROPHY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy", "shortest_name_length": 7}
{"curie": "UMLS:C3273113", "names": ["Gallbladder Adenocarcinoma, Biliary Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gallbladder Adenocarcinoma, Biliary Type", "shortest_name_length": 40}
{"curie": "UMLS:C0743497", "names": ["Endobronchial Mass", "ENDOBRONCHIAL MASS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endobronchial Mass", "shortest_name_length": 18}
{"curie": "UMLS:C3272814", "names": ["Rectal Cribriform Comedo-Type Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rectal Cribriform Comedo-Type Adenocarcinoma", "shortest_name_length": 44}
{"curie": "UMLS:C4525344", "names": ["III", "Stage III Hilar Cholangiocarcinoma", "Stage III Hilar Cholangiocarcinoma AJCC v8", "Stage III Perihilar Cholangiocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Hilar Cholangiocarcinoma AJCC v8", "shortest_name_length": 3}
{"curie": "UMLS:C5419897", "names": ["Digestive System Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Digestive System Diffuse Large B-Cell Lymphoma", "shortest_name_length": 46}
{"curie": "MONDO:0005801", "names": ["HTLV-1", "HTLV-1 infection", "HTLV-1 Infection", "HTLV-I Infection", "HTLV 1 infection", "HTLV-I infection", "HTLV I infection", "HTLV-I infections", "Infection, HTLV-I", "HTLV-I Infections", "HTLV I Infections", "Infections, HTLV-I", "Infections, HTLV I", "Human T lymphotropic virus type 1", "Human T-lymphotropic virus 1 infection", "Human T lymphotropic Virus 1 Infection", "Human T-lymphotropic Virus 1 Infection", "Human T-lymphotropic Virus 1 Infections", "Human T lymphotropic Virus 1 Infections", "T-cell lymphotropic virus type-1; human", "Human T-cell lymphotropic virus 1 infection", "Human T-cell leukemia virus type I infection", "Human T-cell leukaemia virus type I infection", "human T-lymphotropic virus 1 (HTLV-I) infection", "human T-lymphotropic virus 1 infectious disease", "Human T-lymphotropic virus 1 infectious disease", "Human T-lymphotropic virus 1 disease or disorder", "Human T-cell lymphotropic virus type I infection", "Human T-lymphotropic virus 1 infection (disorder)", "Human T-cell lymphotropic virus (HTLV) 1 infection", "Human T-lymphotropic virus 1 caused disease or disorder", "human T-lymphotropic virus 1 (HTLV-I) infection (diagnosis)", "infection; viral, human T-cell lymphotropic virus type-1 (HTLV-1)", "viral; infection, human T-cell lymphotropic virus type-1 (HTLV-1)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "human T-lymphotropic virus 1 infectious disease", "shortest_name_length": 6}
{"curie": "MONDO:0001426", "names": ["mediastinum neurofibroma", "Mediastinal Neurofibroma", "mediastinal neurofibroma", "neurofibroma of mediastinum", "Neurofibroma of mediastinum", "Neurofibroma of Mediastinum", "Neurofibroma of the Mediastinum", "neurofibroma of the mediastinum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mediastinum neurofibroma", "shortest_name_length": 24}
{"curie": "UMLS:C0348616", "names": ["Other restrictive cardiomyopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Other restrictive cardiomyopathy", "shortest_name_length": 32}
{"curie": "MONDO:0017394", "names": ["ketamine-induced biliary dilatation", "Ketamine-induced biliary dilatation", "Dilatation of common bile duct due to harmful use of ketamine", "Dilatation of common bile duct due to harmful use of ketamine (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ketamine-induced biliary dilatation", "shortest_name_length": 35}
{"curie": "MONDO:0000587", "names": ["autoimmune otorhinolaryngologic disease", "autoimmune disease of ear, nose and throat", "autoimmune disease of eyes, ear, nose and throat"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune disease of ear, nose and throat", "shortest_name_length": 39}
{"curie": "UMLS:C4727005", "names": ["Locally Advanced Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Sarcoma", "shortest_name_length": 24}
{"curie": "MONDO:0017040", "names": ["exposure-related interstitial lung disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exposure-related interstitial lung disease", "shortest_name_length": 42}
{"curie": "MONDO:0022409", "names": ["nephropathy-associated ciliopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephropathy-associated ciliopathy", "shortest_name_length": 33}
{"curie": "UMLS:C1709245", "names": ["Non-Neoplastic Anal Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Anal Disorder", "shortest_name_length": 28}
{"curie": "MONDO:0014344", "names": ["CHTD4", "congenital heart defects, multiple types, 4", "CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 4", "NR2F2 congenital heart defects, multiple types", "congenital heart defects, multiple types caused by mutation in NR2F2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital heart defects, multiple types, 4", "shortest_name_length": 5}
{"curie": "UMLS:C0038834", "names": ["SVC Thrombosis", "SVC Thromboses", "Thrombosis, SVC", "Superior vena cava thrombosis", "Superior Vena Cava Thrombosis", "Superior venacaval thrombosis", "Thrombosis of superior vena cava", "thrombosis of superior vena cava", "Thrombosis of superior vena cava (disorder)", "thrombosis of superior vena cava (diagnosis)", "venous thrombosis thoracic veins superior vena cava"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Superior Vena Cava Thrombosis", "shortest_name_length": 14}
{"curie": "MONDO:0013118", "names": ["NBSLD", "RAD50 DEFICIENCY", "RAD50 Deficiency", "Rad50 deficiency", "RAD50 deficiency", "NBs-like disorder", "NBS-LIKE DISORDER", "NBS-like disorder", "Nijmegen breakage syndrome-like disorder", "Nijmegen Breakage Syndrome-Like Disorder", "NIJMEGEN BREAKAGE SYNDROME-LIKE DISORDER", "NBS-like (Nijmegen breakage syndrome-like) disorder", "Nijmegen breakage syndrome-like disorder (disorder)", "Nijmegen breakage syndrome-like disorder (diagnosis)", "microcephaly and chromosomal instability without immunodeficiency", "Microcephaly and chromosomal instability without immunodeficiency", "microcephaly and spontaneous chromosome instability without immunodeficiency", "Microcephaly and Spontaneous Chromosome Instability without Immunodeficiency", "MICROCEPHALY AND SPONTANEOUS CHROMOSOME INSTABILITY WITHOUT IMMUNODEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nijmegen breakage syndrome-like disorder", "shortest_name_length": 5}
{"curie": "MONDO:0013129", "names": ["COD4", "ACHM5", "achromatopsia 5", "ACHROMATOPSIA 5", "Achromatopsia 5", "cone dystrophy 4", "CONE DYSTROPHY 4", "Cone Dystrophy 4", "PDE6C cone dystrophy", "cone dystrophy type 4", "CONE DYSTROPHY 4 (disorder)", "cone dystrophy caused by mutation in PDE6C"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cone dystrophy 4", "shortest_name_length": 4}
{"curie": "UMLS:C2987408", "names": ["Gastric Non-Neoplastic Polyp"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Non-Neoplastic Polyp", "shortest_name_length": 28}
{"curie": "MONDO:0009807", "names": ["osteosarcoma", "osteoid sarcoma", "Skeletal sarcoma", "osteogenic sarcoma", "sarcoma of osteoid", "Osteogenic sarcoma", "Bony Tissue Neoplasm", "Bone Tissue Neoplasm", "bone tissue neoplasm", "Neoplasm, Bony Tissue", "Tissue Neoplasm, Bony", "Tissue Neoplasm, Bone", "Bone Tissue Neoplasms", "Bony Tissue Neoplasms", "Neoplasm, Bone Tissue", "Tissue Neoplasms, Bony", "osteosarcoma (disease)", "Tissue Neoplasms, Bone", "Neoplasms, Bone Tissue", "Neoplasms, Bony Tissue", "osteosarcoma, malignant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteosarcoma", "shortest_name_length": 12}
{"curie": "MONDO:0001833", "names": ["Blocked tear duct", "tear duct blocked", "blocked tear duct", "blocked ducts tear", "tear duct occlusion", "Tear Duct Obstruction", "Duct Obstruction, Tear", "Tear Duct Obstructions", "Obstruction, Tear Duct", "Canalicular obstruction", "lacrimal duct obstruction", "Lacrimal duct obstruction", "LACRIMAL DUCT OBSTRUCTION", "Lacrimal Duct Obstruction", "lacrimal obstruction duct", "Obstruction, Lacrimal Duct", "Duct Obstruction, Lacrimal", "Lacrimal Duct Obstructions", "Lachrymal duct obstruction", "occlusion; lacrimal passages", "blocked lacrimal canaliculus", "Nasolacrimal duct obstructed", "Obstuction of lacrimal ducts", "Obstruction of lacrimal duct", "Blocked lacrimal canaliculus", "lacrimal passages; occlusion", "obstruction of lacrimal ducts", "NASOLACRIMAL DUCT OBSTRUCTION", "Obstruction of lacrimal ducts", "Lacrimal duct obstruction NOS", "Nasolacrimal duct obstruction", "Nasolacrimal Duct Obstruction", "Duct Obstruction, Nasolacrimal", "obstruction; lacrimal passages", "lacrimal passages; obstruction", "Nasolacrimal Duct Obstructions", "obstruction; nasolacrimal duct", "Obstruction, Nasolacrimal Duct", "tear duct occlusion (diagnosis)", "Obstruction of nasolacrimal duct", "Lacrimal canalicular obstruction", "Obstruction of lacrimal canaliculi", "obstruction of lacrimal canaliculus", "Obstruction of lacrimal canaliculus", "Obstruction of nasolacrimal duct (disorder)", "Obstruction of lacrimal canaliculus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lacrimal duct obstruction", "shortest_name_length": 17}
{"curie": "MONDO:0034142", "names": ["pancreatic agenesis-holoprosencephaly syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic agenesis-holoprosencephaly syndrome", "shortest_name_length": 46}
{"curie": "UMLS:C0677702", "names": ["Stage II Grade 2 Follicular Lymphoma", "noncontiguous stage II grade 2 follicular lymphoma", "Stage II Grade 2 Non-Contiguous Follicular Lymphoma", "Non-Contiguous Stage II Grade II Follicular Lymphoma", "Non-Contiguous Grade II Follicular Lymphoma Stage II", "Stage II Non-Contiguous Follicular Mixed Cell Lymphoma", "Non-Contiguous Follicular Mixed Cell Lymphoma Stage II", "Non-Contiguous Stage II Follicular Mixed Cell Lymphoma", "Ann Arbor Stage II Grade 2 Non-Contiguous Follicular Lymphoma", "noncontiguous stage II grade II follicular mixed cell lymphoma", "Non-Contiguous Stage II Grade II Follicular Mixed Cell Lymphoma", "Non-Contiguous Grade II Follicular Mixed Cell Lymphoma Stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage II Grade 2 Non-Contiguous Follicular Lymphoma", "shortest_name_length": 36}
{"curie": "UMLS:C0160414", "names": ["injury of spleen with open wound into cavity", "Injury to Spleen with Open Wound into Cavity", "Injury to spleen with open wound into cavity", "injury of spleen with open wound into cavity (diagnosis)", "Unspecified injury to spleen with open wound into cavity", "Injury to spleen with open wound into cavity, unspecified injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury to spleen with open wound into cavity", "shortest_name_length": 44}
{"curie": "MONDO:0043789", "names": ["serum rash", "Serum rash", "rash; serum", "serum; rash", "serum reaction", "SERUM SICKNESS", "Serum Sickness", "Serum reaction", "Serum sickness", "serum sickness", "sickness, serum", "reaction; serum", "Sickness, Serum", "Serum urticaria", "serum; reaction", "protein sickness", "urticaria; serum", "Protein sickness", "serum; urticaria", "Serum Sicknesses", "serum Sicknesses", "protein; sickness", "Sicknesses, Serum", "Sicknesses, serum", "serum intoxication", "intoxication; serum", "serum; intoxication", "intoxication by serum", "Intoxication by serum", "Serum rash (disorder)", "urticaria due to serum", "Urticaria due to serum", "serum rash (diagnosis)", "Urticaria caused by serum", "serum reaction (diagnosis)", "serum sickness (diagnosis)", "protein sickness (diagnosis)", "serum intoxication (diagnosis)", "Serum sickness due to transfusion", "urticaria due to serum (diagnosis)", "Urticaria caused by serum (disorder)", "transfusion reaction due to serum protein reaction", "Transfusion reaction due to serum protein reaction", "Transfusion reaction due to serum protein reaction, NOS", "Transfusion reaction due to serum protein reaction (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "serum sickness", "shortest_name_length": 10}
{"curie": "UMLS:C0751848", "names": ["Middle Cerebral Artery Thrombotic Infarction", "Thrombotic Infarction, Middle Cerebral Artery"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thrombotic Infarction, Middle Cerebral Artery", "shortest_name_length": 44}
{"curie": "UMLS:C1720772", "names": ["Hypoprebetalipoproteinemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypoprebetalipoproteinemia", "shortest_name_length": 26}
{"curie": "UMLS:C1332504", "names": ["Benign Gastric Soft Tissue Neoplasm", "Benign Soft Tissue Neoplasm of Stomach", "Benign Soft Tissue Neoplasm of the Stomach"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Gastric Soft Tissue Neoplasm", "shortest_name_length": 35}
{"curie": "UMLS:C0393524", "names": ["late-onset ataxia", "ataxia late-onset", "cerebellar ataxia late-onset", "Late-onset cerebellar ataxia", "Late onset cerebellar ataxia", "Late Onset Cerebellar Ataxia", "Cerebellar ataxia, late-onset", "Cerebellar Ataxia, Late Onset", "Late onset cerebellar ataxia (disorder)", "cerebellar ataxia late-onset (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebellar Ataxia, Late Onset", "shortest_name_length": 17}
{"curie": "UMLS:C0345961", "names": ["Lung Epithelioid Angioendothelioma", "Intravascular bronchoalveolar tumor", "Intravascular bronchoalveolar tumour", "Epithelioid Angioendothelioma of Lung", "Lung Epithelioid Hemangioendothelioma", "Intravascular Bronchioloalveolar Tumor", "Pulmonary Epithelioid Angioendothelioma", "Epithelioid hemangioendothelioma of lung", "Epithelioid Hemangioendothelioma of Lung", "Epithelioid haemangioendothelioma of lung", "Epithelioid Angioendothelioma of the Lung", "Pulmonary Epithelioid Hemangioendothelioma", "Epithelioid Hemangioendothelioma of the Lung", "IVBALT - Intravascular bronchoalveolar tumor", "IVBALT - Intravascular bronchoalveolar tumour", "malignant epithelioid hemangioendothelioma of lung", "Epithelioid hemangioendothelioma of lung (disorder)", "malignant epithelioid hemangioendothelioma of lung (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epithelioid hemangioendothelioma of lung", "shortest_name_length": 34}
{"curie": "MONDO:0009964", "names": ["SRTD9", "MZSDS", "Conorenal Syndrome", "Conorenal syndrome", "CONORENAL SYNDROME", "Mainzer-Saldino Disease", "Saldino-Mainzer disease", "Mainzer-Saldino syndrome", "Saldino-Mainzer syndrome", "Mainzer-Saldino Syndrome", "Mainzer Saldino syndrome", "MAINZER-SALDINO SYNDROME", "Saldino-Mainzer dysplasia", "Saldino-Mainzer dysplasia (disorder)", "SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY", "short-rib thoracic dysplasia 9 with or without polydactyly", "renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia", "Renal dysplasia, retinal pigmentory dystrophy, cerebellar ataxia and skeletal dysplasia", "Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia, and skeletal dysplasia", "RENAL DYSPLASIA, RETINAL PIGMENTARY DYSTROPHY, CEREBELLAR ATAXIA, AND SKELETAL DYSPLASIA", "renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia, and skeletal dysplasia", "renal dysplasia-retinal pigmentary dystrophy-cerebellar ataxia-skeletal dysplasia syndrome", "Renal dysplasia-retinal pigmentary dystrophy-cerebellar ataxia-skeletal dysplasia syndrome", "Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia, skeletal dysplasia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short-rib thoracic dysplasia 9 with or without polydactyly", "shortest_name_length": 5}
{"curie": "UMLS:C1882108", "names": ["Non-Neoplastic Stomach Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Stomach Disorder", "shortest_name_length": 31}
{"curie": "MONDO:0054730", "names": ["SPGF26", "SPERMATOGENIC FAILURE 26", "spermatogenic failure 26"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 26", "shortest_name_length": 6}
{"curie": "MONDO:0018842", "names": ["PEL", "AIDS-related lymphoma", "Primary effusion lymphoma", "primary effusion lymphoma", "primary Effusion Lymphoma", "Primary Effusion Lymphoma", "Body cavity-based lymphoma", "Primary Effusion Lymphomas", "body cavity-based lymphoma", "Lymphoma, Primary Effusion", "Effusion Lymphoma, Primary", "Lymphomas, Primary Effusion", "Effusion Lymphomas, Primary", "Primary effusion B-cell lymphoma", "Primary effusion lymphoma (disorder)", "Primary effusion lymphoma (diagnosis)", "Primary effusion lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary effusion lymphoma", "shortest_name_length": 3}
{"curie": "MONDO:0019208", "names": ["Bickerstaff encephalitis", "Bickerstaff's encephalitis", "Bickerstaff brainstem encephalitis", "Bickerstaff's brainstem encephalitis", "Bickerstaff's brainstem encephalitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bickerstaff brainstem encephalitis", "shortest_name_length": 24}
{"curie": "MONDO:0040922", "names": ["Latent early syphilis", "Early Latent Syphilis", "latent early syphilis", "SYPHILIS LATENT EARLY", "Early syphilis, latent", "syphilis; early, latent", "Latent early syphilis (disorder)", "latent early syphilis (diagnosis)", "Early syphilis, latent, unspecified", "Early syphilis, latent, NOS (+ sero., - C.S.F., less than 2 years after)", "early latent syphilis with positive serology, negative spinal fluid, less than 2 years after infection", "Early latent syphilis, positive serology, negative cerebrospinal fluid, less than 2 years after infection", "early latent syphilis with positive serology, negative spinal fluid, less than 2 years after infection (diagnosis)", "Early latent syphilis, positive serology, negative cerebrospinal fluid, less than 2 years after infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "latent early syphilis", "shortest_name_length": 21}
{"curie": "MONDO:0010866", "names": ["Prenatal axonal dystrophy and osteopetrosis", "osteoporosis and infantile neuroaxonal dystrophy", "osteopetrosis and infantile neuroaxonal dystrophy", "Osteopetrosis and infantile neuroaxonal dystrophy", "OSTEOPETROSIS AND INFANTILE NEUROAXONAL DYSTROPHY", "Infantile osteopetrosis with neuroaxonal dysplasia", "CSF1R-related brain malformation and osteopetrosis", "infantile osteopetrosis with neuroaxonal dysplasia", "Infantile osteopetrosis and neuronal storage disease", "Infantile osteopetrosis with neuroaxonal dysplasia syndrome", "Infantile osteopetrosis with neuroaxonal dysplasia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile osteopetrosis with neuroaxonal dysplasia", "shortest_name_length": 43}
{"curie": "MONDO:0021437", "names": ["Gastric lipoma", "gastric lipoma", "stomach lipoma", "Gastric Lipoma", "Lipoma of Stomach", "lipoma of stomach", "Lipoma of stomach", "lipoma of the stomach", "Lipoma of the Stomach", "Lipoma of stomach (disorder)", "lipoma of stomach (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lipoma of stomach", "shortest_name_length": 14}
{"curie": "UMLS:C5206663", "names": ["Penile Epithelioid Hemangioendothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Penile Epithelioid Hemangioendothelioma", "shortest_name_length": 39}
{"curie": "UMLS:C5207968", "names": ["Musculoskeletal toxicity", "Musculoskeletal Toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Musculoskeletal toxicity", "shortest_name_length": 24}
{"curie": "MONDO:0004331", "names": ["urachus adenocarcinoma", "urachal adenocarcinoma", "Urachal adenocarcinoma", "adenocarcinoma of the urachus", "Adenocarcinoma of the urachus", "Bladder Urachal Adenocarcinoma", "bladder urachal adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder urachal adenocarcinoma", "shortest_name_length": 22}
{"curie": "MONDO:0100455", "names": ["neonatal-onset developmental and epileptic encephalopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal-onset developmental and epileptic encephalopathy", "shortest_name_length": 57}
{"curie": "UMLS:C1709159", "names": ["Neoplasm by Obsolete Classification"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplasm by Obsolete Classification", "shortest_name_length": 35}
{"curie": "MONDO:0013309", "names": ["chromosome 2p12-p11.2 deletion syndrome", "CHROMOSOME 2p12-p11.2 DELETION SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 2p12-p11.2 deletion syndrome", "shortest_name_length": 39}
{"curie": "UMLS:C0752293", "names": ["Extrinsic Sleep Disorder", "Extrinsic Sleep Disorders", "Sleep Disorder, Extrinsic", "Sleep Disorders, Extrinsic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sleep Disorders, Extrinsic", "shortest_name_length": 24}
{"curie": "UMLS:C1257796", "names": ["Choledochal Diverticulum", "Choledochal Cyst, Type II", "Choledochal Diverticulums", "Diverticulum, Choledochal", "Diverticulum Choledochal Cyst", "Diverticulum Choledochal Cysts", "Choledochal Cyst, Diverticulum", "Choledochal Cysts, Diverticulum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Choledochal Cyst, Type II", "shortest_name_length": 24}
{"curie": "UMLS:C0400883", "names": ["Intestinal Vascular Disorder", "Intestinal vascular disorder", "vascular disorder of intestine", "Vascular disorder of intestine", "Vascular disorders of intestine", "Vascular Disorders of Intestine", "disease (or disorder); bowel, vascular", "Vascular disorder of intestine (disorder)", "vascular disorder of intestine (diagnosis)", "Vascular disorder of intestine, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vascular disorder of intestine", "shortest_name_length": 28}
{"curie": "MONDO:0013361", "names": ["Dysprothrombinemia", "DYSPROTHROMBINEMIA", "HYPOPROTHROMBINEMIA", "Hypoprothrombinemia", "hypoprothrombinemia", "factor 2 deficiency", "deficiency factor ii", "Factor II deficiency", "factor II deficiency", "Factor II Deficiency", "HYPOPROTHROMBINAEMIA", "Hypoprothrombinaemia", "Hypoprothrombinemias", "hypoprothrombinaemia", "FACTOR II DEFICIENCY", "factor ii deficiency", "Deficiency, factor II", "Deficiency, Factor II", "prothrombin deficiency", "Prothrombin deficiency", "PROTHROMBIN DEFICIENCY", "Factor II Deficiencies", "Prothrombin Deficiency", "Deficiency, Prothrombin", "prothrombin; deficiency", "Deficiencies, Factor II", "deficiency; prothrombin", "Deficiency, prothrombin", "Prothrombin Deficiencies", "Factor II deficiency, NOS", "Deficiencies, Prothrombin", "Prothrombin deficiency, NOS", "Hereditary hypoprothrombinemia", "Hereditary Hypoprothrombinemia", "congenital factor II deficiency", "Hereditary Factor II Deficiency", "Factor II deficiency (disorder)", "Hereditary hypoprothrombinaemia", "Congenital factor II deficiency", "hereditary prothrombin deficiency", "Constitutional dysprothrombinemia", "Hereditary Prothrombin Deficiency", "congenital prothrombin deficiency", "prothrombin deficiency, congenital", "PROTHROMBIN DEFICIENCY, CONGENITAL", "Deficiency of factor II [prothrombin]", "Hereditary factor II deficiency disease", "congenital factor II deficiency (diagnosis)", "congenital factor II (prothrombin) deficiency", "Hereditary factor II deficiency disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital prothrombin deficiency", "shortest_name_length": 18}
{"curie": "UMLS:C0862458", "names": ["Metastatic Ureter Urothelial Cancer", "Urothelial carcinoma ureter metastatic", "Metastatic Ureter Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urothelial carcinoma ureter metastatic", "shortest_name_length": 35}
{"curie": "UMLS:C5556497", "names": ["High-Grade Renal Pelvis Urothelial Carcinoma", "High Grade Renal Pelvis Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Renal Pelvis Urothelial Carcinoma", "shortest_name_length": 44}
{"curie": "UMLS:C4054747", "names": ["Idiopathic Renal Papillary Necrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Idiopathic Renal Papillary Necrosis", "shortest_name_length": 35}
{"curie": "UMLS:C4553418", "names": ["Stage III Bladder Cancer", "Stage III Bladder Cancer AJCC v8", "Stage III Bladder Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Bladder Cancer AJCC v8", "shortest_name_length": 24}
{"curie": "UMLS:C1096243", "names": ["central infection line", "Central Line Infection", "central line infection", "Central line infection", "central infections line"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central line infection", "shortest_name_length": 22}
{"curie": "MONDO:0004826", "names": ["urethral stone", "urethral Stone", "Urethral stone", "Urethral Stone", "stones urethral", "Urethral calculi", "Urethrolithiasis", "urethrolithiasis", "Urethral calculus", "urethral calculus", "URETHRA, CALCULUS", "urethra; calculus", "Urethral Calculus", "CALCULUS URETHRAL", "URETHRAL CALCULUS", "Calculus urethral", "calculus; urethra", "calculus in urethra", "Calculus in urethra", "urethra urolithiasis", "urolithiasis of urethra", "urethral stone (diagnosis)", "Calculus in urethra (disorder)", "calculus in urethra (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urethral calculus", "shortest_name_length": 14}
{"curie": "MONDO:0010517", "names": ["CILD36", "primary ciliary dyskinesia 36", "PIH1D3 primary ciliary dyskinesia", "X-linked primary ciliary dyskinesia 36", "CILIARY DYSKINESIA, PRIMARY, 36, X-LINKED", "ciliary dyskinesia, primary, 36, X-linked", "ciliary dyskinesia, primary, 36, X-linked; CILD36", "primary ciliary dyskinesia caused by mutation in PIH1D3", "ciliary dyskinesia, primary, 36, X-linked, X-linked recessive", "CILIARY DYSKINESIA, PRIMARY, 36, WITH OR WITHOUT SITUS INVERSUS", "ciliary dyskinesia, primary, 36, with or without situs inversus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ciliary dyskinesia, primary, 36, X-linked", "shortest_name_length": 6}
{"curie": "MONDO:0020561", "names": ["MRCLS", "myxoid/round cell liposarcoma", "myxoid/round-cell liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myxoid/round cell liposarcoma", "shortest_name_length": 5}
{"curie": "UMLS:C0866112", "names": ["Nephrotic syndrome with lesion of hypocomplementemic glomerulonephritis", "Nephrotic Syndrome with Lesion of Hypocomplementemic Glomerulonephritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome with Lesion of Hypocomplementemic Glomerulonephritis", "shortest_name_length": 71}
{"curie": "MONDO:0009741", "names": ["NBLST1", "susceptibility to neuroblastoma", "neuroblastoma, susceptibility to", "NEUROBLASTOMA, SUSCEPTIBILITY TO", "NEUROBLASTOMA, SUSCEPTIBILITY TO, 1", "neuroblastoma, susceptibility to, 1", "NEUROBLASTOMA, SUSCEPTIBILITY TO, 1 (disorder)", "neuroblastoma, susceptibility to, 1, autosomal dominant, somatic mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuroblastoma, susceptibility to, 1", "shortest_name_length": 6}
{"curie": "MONDO:0013561", "names": ["gPAPP deficiency", "GPAPP DEFICIENCY", "chondrodysplasia with joint dislocations gPAPP type", "Chondrodysplasia with joint dislocations gPAPP type", "chondrodysplasia with joint dislocations, gPAPP type", "CHONDRODYSPLASIA WITH JOINT DISLOCATIONS, GPAPP TYPE", "Chondrodysplasia with joint dislocations, gPAPP type", "Chondrodysplasia with joint dislocations gPAPP type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chondrodysplasia with joint dislocations, gPAPP type", "shortest_name_length": 16}
{"curie": "MONDO:0017334", "names": ["Deletion 12q15q21.1", "Monosomy 12q15q21.1", "Del(12)(q15)(q21.1)", "monosomy 12q15q21.1", "deletion 12q15q21.1", "12q15q21.1 microdeletion syndrome", "12q15q21.1 microdeletion syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "12q15q21.1 microdeletion syndrome", "shortest_name_length": 19}
{"curie": "MONDO:0100067", "names": ["childhood spindle cell rhabdomyosarcoma", "Childhood Spindle Cell Rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood spindle cell rhabdomyosarcoma", "shortest_name_length": 39}
{"curie": "MONDO:0003808", "names": ["Mediastinal Osteosarcoma", "mediastinal osteosarcoma", "osteosarcoma of mediastinum", "Osteosarcoma of Mediastinum", "Osteosarcoma of mediastinum", "mediastinal osteogenic sarcoma", "Mediastinal Osteogenic Sarcoma", "osteosarcoma of the mediastinum", "Osteosarcoma of the Mediastinum", "Osteogenic Sarcoma of Mediastinum", "osteogenic sarcoma of mediastinum", "mediastinum osteosarcoma (disease)", "Osteogenic Sarcoma of the Mediastinum", "osteogenic sarcoma of the mediastinum", "mediastinal extraskeletal osteosarcoma", "Mediastinal Extraskeletal Osteosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mediastinal extraskeletal osteosarcoma", "shortest_name_length": 24}
{"curie": "MONDO:0007977", "names": ["MDK", "Mdk", "MMDK", "Kantaputra Gorlin syndrome", "Mesomelic dysplasia Thai type", "mesomelic dysplasia Thai type", "MESOMELIC DYSPLASIA, THAI TYPE", "Mesomelic dysplasia, Thai type", "mesomelic dysplasia, Thai type", "Kantaputra mesomelic dysplasia", "Mesomelic dysplasia Kantaputra type", "mesomelic dysplasia Kantaputra type", "Mesomelic dysplasia, Kantaputra type", "MESOMELIC DYSPLASIA, KANTAPUTRA TYPE", "mesomelic dysplasia, Kantaputra type", "Mesomelic dysplasia Kantaputra type (disorder)", "mesomelic dysplasia with ankle carpal and tarsal synostosis", "Mesomelic dysplasia with ankle, carpal, and tarsal synostosis", "mesomelic dysplasia with ankle, carpal, and tarsal synostosis", "MESOMELIC DYSPLASIA WITH ANKLE, CARPAL, AND TARSAL SYNOSTOSIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mesomelic dysplasia, Kantaputra type", "shortest_name_length": 3}
{"curie": "UMLS:C1333953", "names": ["Helicobacter Pylori-Related Malignancy", "Helicobacter Pylori-Related Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Helicobacter Pylori-Related Malignant Neoplasm", "shortest_name_length": 38}
{"curie": "MONDO:0002813", "names": ["lipomatous cancer", "adipose tissue cancer", "cancer of adipose tissue", "malignant lipomatous tumor", "Malignant Lipomatous Neoplasm", "malignant lipomatous neoplasm", "malignant adipose tissue tumor", "malignant adipose tissue neoplasm", "malignant tumor of adipose tissue", "malignant neoplasm of adipose tissue", "malignant tumor of the adipose tissue", "malignant neoplasm of the adipose tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lipomatous cancer", "shortest_name_length": 17}
{"curie": "MONDO:0006285", "names": ["Major Salivary Gland Carcinoma ex Pleomorphic Adenoma", "major salivary gland carcinoma ex pleomorphic adenoma", "carcinoma ex pleomorphic adenoma of Major salivary gland", "Carcinoma ex Pleomorphic Adenoma of Major Salivary Gland", "carcinoma ex pleomorphic adenoma of the Major salivary gland", "Carcinoma ex Pleomorphic Adenoma of the Major Salivary Gland", "major salivary gland salivary gland carcinoma ex pleomorphic adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "major salivary gland carcinoma ex pleomorphic adenoma", "shortest_name_length": 53}
{"curie": "UMLS:C0279972", "names": ["stage II ovarian germ cell tumor", "Stage II Ovarian Germ Cell Tumor", "ovarian germ cell tumor, stage II", "germ cell tumor, ovarian, stage II", "Stage II Ovarian Germ Cell Tumor AJCC v7", "Stage II Ovarian Germ Cell Tumor AJCC v6", "Stage II Malignant Ovarian Germ Cell Tumor", "Stage II Malignant Germ Cell Tumor of Ovary", "Stage II Malignant Ovarian Germ Cell Neoplasm", "Stage II Malignant Germ Cell Neoplasm of Ovary", "Stage II Malignant Germ Cell Tumor of the Ovary", "Stage II Ovarian Germ Cell Tumor AJCC v6 and v7", "Stage II Malignant Germ Cell Neoplasm of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Ovarian Germ Cell Tumor AJCC v6 and v7", "shortest_name_length": 32}
{"curie": "MONDO:0017842", "names": ["SLSN", "Senior Loken syndrome", "Senior-Loken Syndrome", "Loken Senior syndrome", "Senior-Loken syndrome", "Senior Loken Syndrome", "renal-retinal syndrome", "renal dysplasia retinal aplasia", "nephronophthisis with retinal dystrophy", "renal dysplasia-retinal aplasia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Senior-Loken syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C3897083", "names": ["Stage IV Primary Peritoneal Cancer", "Stage IV Primary Peritoneal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Primary Peritoneal Cancer AJCC v7", "shortest_name_length": 34}
{"curie": "UMLS:C5237055", "names": ["Recurrent Endometrial Transitional Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Endometrial Transitional Cell Carcinoma", "shortest_name_length": 49}
{"curie": "MONDO:0009484", "names": ["PCD", "CILD1", "Siewert syndrome", "Kartagener syndrome", "immotile cilia syndrome", "Polynesian bronchiectasis", "primary ciliary dyskinesia 1", "Primary Ciliary Dyskinesia 1", "CILIARY DYSKINESIA, PRIMARY, 1", "Ciliary Dyskinesia, Primary, 1", "ciliary dyskinesia, primary, 1", "DNAI1 primary ciliary dyskinesia", "primary ciliary dyskinesia type 1", "ciliary dyskinesia, primary, type 1", "dextrocardia, bronchiectasis, and sinusitis", "primary ciliary dyskinesia caused by mutation in DNAI1", "primary ciliary dyskinesia 1 with or without situs inversus", "ciliary dyskinesia, primary, 1, with or without situs inversus", "CILIARY DYSKINESIA, PRIMARY, 1, WITH OR WITHOUT SITUS INVERSUS", "Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia 1", "shortest_name_length": 3}
{"curie": "MONDO:0005784", "names": ["hfr", "hfrs", "HFRS", "Korean hemorrhagic fever", "korean hemorrhagic fever", "Muroid virus nephropathy", "Korean Hemorrhagic Fever", "fever hemorrhagic korean", "Puumala virus nephropathy", "Hemorrhagic fever, Korean", "Hantaan virus nephropathy", "Korean haemorrhagic fever", "Russian hemorrhagic fever", "Hemorrhagic Fever, Korean", "Myhrman-Zetterholm disease", "Hemorrhagic fever, Russian", "Epidemic Hemorrhagic Fever", "hemorrhagic fever, Russian", "Epidemic hemorrhagic fever", "Russian haemorrhagic fever", "Epidemic Hemorrhagic Fevers", "Hemorrhagic Fever, Epidemic", "Hemorrhagic fever, epidemic", "Epidemic haemorrhagic fever", "epidemic haemorrhagic fever", "HEMORRHAGIC FEVER, EPIDEMIC", "Hemorrhagic Fevers, Epidemic", "nephrosonephritis hemorrhagic", "Hemorrhagic nephrosonephritis", "hemorrhagic nephrosonephritis", "Hemorrhagic Nephroso Nephritis", "Hemorrhagic Nephroso-Nephritis", "Hemorrhagic nephroso-nephritis", "Haemorrhagic nephrosonephritis", "MVN - Muroid virus nephropathy", "Hanta virus infection (korean)", "NEPHROSONEPHRITIS, HEMORRHAGIC", "KHF - Korean hemorrhagic fever", "KHF - Korean haemorrhagic fever", "Haemorrhagic nephroso-nephritis", "Nephroso-Nephritis, Hemorrhagic", "fever hemorrhagic renal syndrome", "Hemorrhagic Nephroso-Nephritides", "Nephroso-Nephritides, Hemorrhagic", "HNN - Hemorrhagic nephrosonephritis", "Puumala virus nephropathy (disorder)", "HNN - Haemorrhagic nephrosonephritis", "Hemorrhagic Fever with Renal Syndrome", "HEMORRHAGIC FEVER WITH RENAL SYNDROME", "Hemorrhagic fever with renal syndrome", "hemorrhagic fever with renal syndrome", "Haemorrhagic fever with renal syndrome", "Hemorrhagic nephrosonephritis (diagnosis)", "HFRS - hemorrhagic fever with renal syndrome", "HFRS (hemorrhagic fever with renal syndrome)", "HFRS - Hemorrhagic fever with renal syndrome", "HFRS - Haemorrhagic fever with renal syndrome", "HFRS - haemorrhagic fever with renal syndrome", "hantavirus hemorrhagic fever with renal syndrome", "nephrosis; epidemic hemorrhagic fever (etiology)", "Hemorrhagic fever with renal syndrome (disorder)", "Hantavirus hemorrhagic fever with renal syndrome", "epidemic; hemorrhagic fever, nephrosis (etiology)", "hemorrhagic fever with renal syndrome (diagnosis)", "nephrosis; epidemic hemorrhagic fever (manifestation)", "epidemic; hemorrhagic fever, nephrosis (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hantavirus hemorrhagic fever with renal syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C1336880", "names": ["Ureteral Transitional Cell Carcinoma with Glandular Differentiation", "Transitional Cell Carcinoma of Ureter with Glandular Differentiation", "Infiltrating Ureter Urothelial Carcinoma with Glandular Differentiation", "Transitional Cell Carcinoma of the Ureter with Glandular Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infiltrating Ureter Urothelial Carcinoma with Glandular Differentiation", "shortest_name_length": 67}
{"curie": "UMLS:C1112501", "names": ["Colorectal MP", "Colorectal HP", "Colorectal Metaplastic Polyp", "Colorectal Hyperplastic Polyp", "Colorectal hyperplastic polyp", "Hyperplastic Large Bowel Polyp", "Hyperplastic Polyp of Large Bowel", "Hyperplastic Polyp of the Large Bowel"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal hyperplastic polyp", "shortest_name_length": 13}
{"curie": "MONDO:0012921", "names": ["T1D22", "IDDM22", "type 1 diabetes mellitus 22", "TYPE 1 DIABETES MELLITUS 22", "CCR5 type 1 diabetes mellitus", "Insulin-Dependent Diabetes Mellitus 22", "insulin-dependent diabetes mellitus 22", "Diabetes Mellitus, Insulin-Dependent, 22", "DIABETES MELLITUS, INSULIN-DEPENDENT, 22", "diabetes mellitus, insulin-dependent, 22", "diabetes mellitus, insulin-dependent, type 22", "type 1 diabetes mellitus caused by mutation in CCR5", "DIABETES MELLITUS, INSULIN-DEPENDENT, 22 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type 1 diabetes mellitus 22", "shortest_name_length": 5}
{"curie": "MONDO:0007045", "names": ["AFD Catania type", "Afd, Catania type", "AFD, CATANIA TYPE", "Opitz-Caltabiano syndrome", "Opitz Caltabiano syndrome", "Opitz Mollica Sorge syndrome", "acrofacial dysostosis Catania type", "Acrofacial dysostosis Catania type", "Acrofacial dysostosis Catania form", "acrofacial dysostosis, Catania type", "Acrofacial dysostosis, Catania type", "Acrofacial Dysostosis, Catania Type", "ACROFACIAL DYSOSTOSIS, CATANIA TYPE", "acrofacial dysostosis (ACD), Catania type", "Acrofacial dysostosis Catania type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acrofacial dysostosis, Catania type", "shortest_name_length": 16}
{"curie": "UMLS:C0157259", "names": ["Prolonged 1st stage", "Active Phase Arrest", "long; delivery, first stage", "labor; arrested active phase", "labor; prolonged, first stage", "arrest; active phase of labor", "Prolonged First Stage of Labor", "prolonged first stage of labor", "arrested active phase of labor", "Prolonged first stage of labor", "Arrested active phase of labor", "Prolonged first stage of labour", "Arrested active phase of labour", "Arrest of Labor in Active Phase", "Prolonged Active Phase of Labor", "arrested; labor in active phase", "Prolonged first stage (of labor)", "prolonged; delivery, first stage", "delivery; prolonged, first stage", "Prolonged first stage (of labour)", "Prolonged first stage of labor (disorder)", "Arrested active phase of labor (disorder)", "prolonged first stage of labor (diagnosis)", "arrested active phase of labor (diagnosis)", "labor; prolonged or protracted, first stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arrested active phase of labor", "shortest_name_length": 19}
{"curie": "UMLS:C0339968", "names": ["neonatal pneumonia", "Neonatal pneumonia", "pneumonia neonatal", "neonatal; pneumonia", "pneumonia; neonatal", "Neonatal pneumonia (disorder)", "neonatal pneumonia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neonatal pneumonia", "shortest_name_length": 18}
{"curie": "UMLS:C3272656", "names": ["Cystic urethritis", "Urethritis cystica", "Urethritis Cystica", "Cystic urethritis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cystic urethritis", "shortest_name_length": 17}
{"curie": "UMLS:C4054547", "names": ["Megacystis - Megaureter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Megacystis - Megaureter", "shortest_name_length": 23}
{"curie": "MONDO:0015051", "names": ["tubular duplication of the esophagus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tubular duplication of the esophagus", "shortest_name_length": 36}
{"curie": "UMLS:C4687700", "names": ["Pericardial Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pericardial Sarcoma", "shortest_name_length": 19}
{"curie": "MONDO:0019765", "names": ["Celosomia", "celosomia", "Celosomus", "Kelosomia", "Celosomus (disorder)", "Celosomial monster, NOS", "Thoracoabdominal eventration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "celosomia", "shortest_name_length": 9}
{"curie": "UMLS:C5556673", "names": ["Cervical Micropapillary Adenocarcinoma", "Invasive Cervical Micropapillary Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Micropapillary Adenocarcinoma", "shortest_name_length": 38}
{"curie": "MONDO:0021805", "names": ["mesomelic dwarfism Campailla-Martinelli type", "Mesomelic dwarfism Campailla-Martinelli type", "Acromesomelic dysplasia Campailla-Martinelli type", "acromesomelic dysplasia Campailla Martinelli type", "Acromesomelic dysplasia Campailla Martinelli type", "acromesomelic dysplasia, Campailla Martinelli type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acromesomelic dysplasia, Campailla Martinelli type", "shortest_name_length": 44}
{"curie": "MONDO:0013509", "names": ["MRD6", "autosomal dominant mental retardation 6", "mental retardation, autosomal dominant 6", "autosomal dominant intellectual disability 6", "intellectual disability, autosomal dominant 6", "mental retardation, autosomal dominant type 6", "intellectual disability, autosomal dominant type 6", "autosomal dominant intellectual developmental disorder 6", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 6", "autosomal dominant non-syndromic intellectual disability 6", "GRIN2B autosomal dominant non-syndromic intellectual disability", "mental retardation, autosomal dominant 6, with or without seizures", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES", "intellectual disability, autosomal dominant 6, with or without seizures", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES", "intellectual developmental disorder, autosomal dominant 6, with or without seizures", "autosomal dominant non-syndromic intellectual disability caused by mutation in GRIN2B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 6", "shortest_name_length": 4}
{"curie": "UMLS:C0549453", "names": ["Hematoma traumatic", "Traumatic hematoma", "TRAUMATIC HEMATOMA", "Haematoma traumatic", "TRAUMATIC HAEMATOMA", "Traumatic haematoma", "Traumatic hematoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Traumatic hematoma", "shortest_name_length": 18}
{"curie": "UMLS:C2981719", "names": ["stage IIIB mycosis fungoides/Sezary syndrome", "Stage IIIB Mycosis Fungoides and Sézary Syndrome", "Stage IIIB Mycosis Fungoides and Sezary Syndrome", "Stage IIIB Mycosis Fungoides and Sézary Syndrome AJCC v7", "stage IIIB mycosis fungoides and Sezary syndrome AJCC v7", "Stage IIIB Mycosis Fungoides and Sezary Syndrome AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Mycosis Fungoides and Sezary Syndrome AJCC v7", "shortest_name_length": 44}
{"curie": "UMLS:C0279542", "names": ["Adult MCHD", "HDMC, adult", "MCHD, adult", "HD MC, adult", "MC HD, adult", "mixed cellularity, HD, adult", "HD, mixed cellularity, adult", "Adult Mixed Cellularity Hodgkin Lymphoma", "adult mixed cellularity Hodgkin lymphoma", "Adult Mixed Cellularity Hodgkin's Disease", "mixed cellularity adult Hodgkin's disease", "adult mixed cellularity Hodgkin's disease", "adult Hodgkin's disease, mixed cellularity", "Adult Mixed Cellularity Hodgkin's Lymphoma", "Hodgkin's disease, mixed cellularity, adult", "mixed cellularity, Hodgkin's disease, adult", "lymphoma, mixed cellularity adult Hodgkin's", "Mixed Cellularity Classical Hodgkin Lymphoma", "Hodgkin's lymphoma, mixed cellularity, adult", "Adult Mixed Cellularity Classic Hodgkin Lymphoma", "Adult Mixed Cellularity Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Mixed Cellularity Classical Hodgkin Lymphoma", "shortest_name_length": 10}
{"curie": "MONDO:0009616", "names": ["Microcephalic primordial dwarfism and cataracts", "microcephalic primordial dwarfism Toriello type", "Microcephalic primordial dwarfism Toriello type", "microcephalic primordial dwarfism and cataracts", "Microcephalic Primordial Dwarfism, Toriello Type", "Microcephalic primordial dwarfism, Toriello type", "microcephalic primordial dwarfism, Toriello type", "MICROCEPHALIC PRIMORDIAL DWARFISM, TORIELLO TYPE", "Microcephalic primordial dwarfism of Toriello type", "Microcephalic primordial dwarfism of Toriello type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephalic primordial dwarfism, Toriello type", "shortest_name_length": 47}
{"curie": "EFO:0009130", "names": ["clostridium difficile infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "clostridium difficile infection", "shortest_name_length": 31}
{"curie": "UMLS:C4763736", "names": ["Refractory Barrett Esophagus", "Refractory Barrett Dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Barrett Esophagus", "shortest_name_length": 28}
{"curie": "UMLS:C5237058", "names": ["Refractory Endometrial Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Endometrial Squamous Cell Carcinoma", "shortest_name_length": 46}
{"curie": "MONDO:0019509", "names": ["hypersensitivity angiitis", "leukocytoclastic angiitis", "cutaneous small-vessel vasculitis", "Cutaneous small vessel vasculitis", "Cutaneous Small Vessel Vasculitis", "cutaneous small vessel vasculitis", "Cutaneous Small-Vessel Vasculitis", "cutaneous leukocytoclastic angiitis", "cutaneous leukocytoclastic vasculitis", "Cutaneous Leukocytoclastic Vasculitis", "cutaneous hypersensitivity vasculitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous leukocytoclastic angiitis", "shortest_name_length": 25}
{"curie": "MONDO:0004426", "names": ["frontal convexity meningioma", "Frontal Convexity Meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontal convexity meningioma", "shortest_name_length": 28}
{"curie": "UMLS:C5555186", "names": ["Refractory Primary Peritoneal Clear Cell Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Primary Peritoneal Clear Cell Adenocarcinoma", "shortest_name_length": 55}
{"curie": "MONDO:0002105", "names": ["Acute megacolon", "Toxic Megacolon", "Megacolon toxic", "Toxic megacolon", "toxic megacolon", "MEGACOLON TOXIC", "toxic; megacolon", "Megacolon, Toxic", "megacolon; toxic", "Toxic dilatation of colon", "Toxic megacolon (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "toxic megacolon", "shortest_name_length": 15}
{"curie": "MONDO:0007208", "names": ["BOOMD", "Piepkorn Dysplasia", "Boomerang dysplasia", "BOOMERANG DYSPLASIA", "Boomerang dysplasia (disorder)", "Boomerang-like skeletal dysplasia", "Dwarfism with short, bowed, rigid limbs and characteristic facies", "dwarfism with short, bowed, rigid limbs and characteristic facies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Boomerang dysplasia", "shortest_name_length": 5}
{"curie": "MONDO:8000000", "names": ["infectious discitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infectious discitis", "shortest_name_length": 19}
{"curie": "MONDO:0011023", "names": ["HMPS", "hereditary mixed polyposis syndrome", "Polyposis Syndrome, Hereditary Mixed, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary mixed polyposis syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0000286", "names": ["EBV hepatitis", "ebv hepatitis", "hepatitis ebv", "hepatitis due to EBV", "hepatitis Epstein-Barr", "Epstein-Barr hepatitis", "Epstein-Barr virus hepatitis", "EBV - Epstein-Barr virus hepatitis", "hepatitis due to Epstein-Barr virus", "Epstein-Barr virus hepatitis (disorder)", "hepatitis due to Epstein-Barr virus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epstein-Barr virus hepatitis", "shortest_name_length": 13}
{"curie": "UMLS:C0332426", "names": ["Lymphoma stage II", "Lymphoma Stage II", "Stage II Lymphoma", "Lymphoma stage II (finding)", "Ann Arbor Stage II Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoma stage II", "shortest_name_length": 17}
{"curie": "MONDO:0005406", "names": ["gdm", "GDM", "MATERNAL DIABETES", "maternal diabetes", "Maternal diabetes", "diabetes pregnancy", "Gestational diabetes", "Gestational Diabetes", "gestational diabetes", "Diabetes in Pregnancy", "diabetes in pregnancy", "Diabetes, Gestational", "maternal hyperglycemia", "Diabetes gestatational", "Diabetes and Pregnancy", "Diabetes;during pregnancy", "diabetes during pregnancy", "pregnancy-induced diabetes", "pregnancy induced diabetes", "Pregnancy-Induced Diabetes", "Diabetes, Pregnancy-Induced", "Diabetes, Pregnancy Induced", "DIABETES MELLITUS GESTATIONAL", "gestational diabetes mellitus", "Diabetes mellitus gestational", "Gestational diabetes mellitus", "Gestational Diabetes Mellitus", "Diabetes Mellitus, Gestational", "DIABETES MELLITUS (GESTATIONAL)", "Gestational diabetes mellitus NOS", "Gestational diabetes mellitus, NOS", "GDM - Gestational diabetes mellitus", "Diabetes mellitus, pregnancy related", "Diabetes mellitus arising in pregnancy", "maternal gestational diabetes mellitus", "Maternal gestational diabetes mellitus", "Gestational diabetes mellitus (disorder)", "gestational diabetes mellitus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gestational diabetes", "shortest_name_length": 3}
{"curie": "UMLS:C1377678", "names": ["adult CNS tumor", "Adult CNS Tumor", "CNS tumor, adult", "Adult CNS Tumors", "Tumor of Adult CNS", "Adult CNS Neoplasm", "Adult CNS Neoplasms", "Neoplasm of Adult CNS", "Tumor of the Adult CNS", "Neoplasm of the Adult CNS", "Central Nervous System Neoplasm", "Adult Central Nervous System Tumor", "Adult Central Nervous System Tumors", "central nervous system tumor, adult", "Tumor of Adult Central Nervous System", "Adult Central Nervous System Neoplasm", "Adult Central Nervous System Neoplasms", "Neoplasm of Adult Central Nervous System", "Tumor of the Adult Central Nervous System", "Neoplasm of the Adult Central Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Central Nervous System Neoplasm", "shortest_name_length": 15}
{"curie": "UMLS:C0278486", "names": ["breast cancer stage ii", "stage II breast cancer", "stage ii breast cancer", "breast cancer ii stage", "Breast cancer stage II", "breast cancer, stage II", "Breast carcinoma stage II", "Carcinoma breast stage II", "Breast cancer NOS stage II", "Breast carcinoma NOS stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast cancer stage II", "shortest_name_length": 22}
{"curie": "MONDO:0008421", "names": ["SIMOSA CRANIOFACIAL SYNDROME", "SIMOSA craniofacial syndrome", "Simosa craniofacial syndrome", "Simosa cranio facial syndrome", "Simosa Penchaszadeh Bustos syndrome", "Simosa-Penchaszadeh-Bustos syndrome", "Flat face-microstomia-ear anomaly syndrome", "flat face-microstomia-ear anomaly syndrome", "Flat face, microstomia, ear anomaly syndrome", "blepharophimosis-telecanthus-microstomia syndrome", "Blepharophimosis-telecanthus-microstomia syndrome", "Blepharophimosis, telecanthus, microstomia syndrome", "Flat face, microstomia, ear anomaly syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "flat face-microstomia-ear anomaly syndrome", "shortest_name_length": 28}
{"curie": "UMLS:C5419165", "names": ["COVID-19-Associated Nervous System Disorder", "SARS-CoV-2 -Associated Nervous System Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "COVID-19-Associated Nervous System Disorder", "shortest_name_length": 43}
{"curie": "MONDO:0009949", "names": ["PC DEFICIENCY", "Pc deficiency", "PC deficiency", "Ataxia with Lactic Acidosis 2", "ataxia with lactic acidosis 2", "Ataxia with lactic acidosis II", "ATAXIA WITH LACTIC ACIDOSIS II", "Ataxia with Lactic Acidosis II", "Pyruvate Carboxylase Deficiency", "PYRUVATE CARBOXYLASE DEFICIENCY", "pyruvate carboxylase deficiency", "Pyruvate carboxylase deficiency", "deficiency; pyruvate carboxylase", "Deficiency, Pyruvate Carboxylase", "pyruvate; carboxylase, deficiency", "Deficiency of pyruvic carboxylase", "carboxylase; pyruvate, deficiency", "deficiency of pyruvic carboxylase", "ataxia with lactic acidosis type 2", "Deficiency of pyruvate carboxylase", "Ataxia with lactic acidosis type 2", "Type II Ataxia with Lactic Acidosis", "Ataxia with lactic acidosis type II", "Leigh syndrome due to PC deficiency", "ataxia with lactic acidosis type II", "Ataxia with Lactic Acidosis, Type II", "PC - Pyruvate carboxylase deficiency", "Lactic Acidosis with Ataxia, Type II", "pyruvate carboxylase deficiency disease", "Pyruvate Carboxylase Deficiency Disease", "Deficiency Disease, Pyruvate Carboxylase", "Pyruvate carboxylase deficiency (disorder)", "pyruvate carboxylase deficiency (diagnosis)", "Leigh syndrome due to pyruvate carboxylase deficiency", "LEIGH SYNDROME DUE TO PYRUVATE CARBOXYLASE DEFICIENCY", "Leigh necrotizing encephalopathy due to pyruvate carboxylase deficiency", "LEIGH NECROTIZING ENCEPHALOPATHY DUE TO PYRUVATE CARBOXYLASE DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyruvate carboxylase deficiency disease", "shortest_name_length": 13}
{"curie": "MONDO:0006520", "names": ["Achenbach Syndrome", "Achenbach syndrome", "Achenbach's syndrome", "Paroxysmal hematoma of the finger", "paroxysmal hematoma of the finger", "Paroxysmal haematoma of the finger", "Paroxysmal hematoma of the finger (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Achenbach syndrome", "shortest_name_length": 18}
{"curie": "MONDO:0011997", "names": ["HPS2", "HPS-2", "Hermansky-Pudlak syndrome 2", "HERMANSKY-PUDLAK SYNDROME 2", "Hermansky Pudlak syndrome 2", "Hermansky-Pudlak Syndrome 2", "AP3B1 Hermansky-Pudlak syndrome", "Hermansky-Pudlak syndrome type 2", "Hermansky-Pudlak syndrome with neutropenia", "Platelet defects and oculocutaneous albinism", "Hermansky-Pudlak syndrome due to AP-3 deficiency", "Hermansky-Pudlak syndrome caused by mutation in AP3B1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hermansky-Pudlak syndrome 2", "shortest_name_length": 4}
{"curie": "MONDO:0016414", "names": ["Lopes-Marques de Faria syndrome", "hypotrichosis-intellectual disability, Lopes type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotrichosis-intellectual disability, Lopes type", "shortest_name_length": 31}
{"curie": "MONDO:0700105", "names": ["difference of sexual differentiation, non-human animal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "difference of sexual differentiation, non-human animal", "shortest_name_length": 54}
{"curie": "UMLS:C0424786", "names": ["postoperative fever", "Postoperative fever", "fever; postoperative", "postoperative; fever", "Postoperative fever (finding)", "postoperative fever (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postoperative fever", "shortest_name_length": 19}
{"curie": "MONDO:0001379", "names": ["Uteric Orifice", "Ureteric Orifice", "URETERIC ORIFICE", "Ureteric orifice", "Ureteral Opening", "Orifice of the Ureter", "orifice of the ureter", "ureteral orifice cancer", "ureteric orifice cancer", "cancer of ureteric orifice", "cancer of ureteral orifice", "malignant tumor of ureteric orifice", "malignant ureteral orifice neoplasm", "Malignant tumor of ureteric orifice", "Malignant tumour of ureteric orifice", "malignant neoplasm of ureteral orifice", "malignant neoplasm of ureteric orifice", "Malignant neoplasm of ureteric orifice", "Malignant tumor of ureteric orifice (disorder)", "malignant neoplasm of ureteric orifice (diagnosis)", "Malignant neoplasm of ureteric orifice of urinary bladder", "malignant neoplasm of ureteric orifice of urinary bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ureteric orifice cancer", "shortest_name_length": 14}
{"curie": "MONDO:0010574", "names": ["PGS", "MRX59", "MRXSF", "MRXS5", "MRXS21", "fried syndrome", "Fried syndrome", "Pettigrew syndrome", "Pettigrew Syndrome", "PETTIGREW SYNDROME", "PETTIGREW syndrome", "Pettigrew syndrome (PGS)", "X-linked mental retardation 59", "Mental Retardation, X-Linked 59", "MENTAL RETARDATION, X-LINKED 59", "mental retardation, X-linked 59", "X-linked intellectual disability 59", "intellectual disability, X-linked 59", "Pettigrew syndrome, X-linked recessive", "X-linked mental retardation syndrome 5", "mental retardation X-linked syndromic 5", "Mental retardation, X-linked syndromic 5", "mental retardation, X-linked syndromic 5", "syndromic X-linked mental retardation 21", "Mental retardation, X-linked, syndromic 5", "MENTAL RETARDATION, X-LINKED, SYNDROMIC 5", "mental retardation, X-linked, syndromic 5", "mental retardation, X-linked, syndromic 21", "MENTAL RETARDATION, X-LINKED, SYNDROMIC 21", "syndromic X-linked intellectual disability 5", "intellectual disability X-linked syndromic 5", "intellectual disability, X-linked syndromic 5", "syndromic X-linked intellectual disability 21", "X-linked mental retardation syndrome 5 (MRXS5)", "intellectual disability, X-linked, syndromic 5", "intellectual disability, X-linked, syndromic 21", "syndromic X-linked mental retardation Fried type", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 59", "syndromic X-linked mental retardation fried type", "syndromic X-linked intellectual disability type 5", "MENTAL RETARDATION, X-LINKED, SYNDROMIC, FRIED TYPE", "mental retardation, X-linked, syndromic, fried type", "syndromic X-linked intellectual disability fried type", "intellectual disability, X-linked, syndromic, fried type", "Dandy-Walker malformation-basal ganglia disease-seizures syndrome", "Dandy-Walker malformation with mental retardation, basal ganglia disease, and seizures", "Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizures", "X-linked intellectual disability-hypotonia-facial dysmorphism-aggressive behavior syndrome", "mental retardation X-linked with Dandy-Walker malformation basal ganglia disease and seizures", "X-linked metal retardation with Dandy-Walker malformation, basal ganglia disease, and seizures", "X-linked intellectual disability - Dandy-Walker malformation - basal ganglia disease - seizures", "Mental retardation, X-linked, with Dandy-Walker malformation, basal ganglia disease, and seizures", "MENTAL RETARDATION, X-LINKED, WITH DANDY-WALKER MALFORMATION, BASAL GANGLIA DISEASE, AND SEIZURES", "mental retardation, X-linked, with Dandy-Walker malformation, basal ganglia disease, and seizures", "intellectual disability X-linked with Dandy-Walker malformation basal ganglia disease and seizures", "X-linked intellectual disability-Dandy-Walker malformation-basal ganglia disease-seizures syndrome", "intellectual disability, X-linked, with Dandy-Walker malformation, basal ganglia disease, and seizures", "X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizure syndrome", "X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizure syndrome (disorder)", "X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizure syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic X-linked intellectual disability 5", "shortest_name_length": 3}
{"curie": "MONDO:0012255", "names": ["Chromosome 18 Pericentric Inversion", "CHROMOSOME 18 PERICENTRIC INVERSION", "chromosome 18 pericentric inversion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 18 pericentric inversion", "shortest_name_length": 35}
{"curie": "MONDO:0019196", "names": ["Foix-Alajouanine syndrome", "Subacute necrotizing myelitis", "Subacute Necrotizing Myelitis", "Subacute necrotising myelitis", "Myelitis, Subacute Necrotizing", "Necrotizing Myelitis, Subacute", "Subacute Necrotizing Myelitides", "Necrotizing Myelitides, Subacute", "Myelitides, Subacute Necrotizing", "angiodysgenetic necrotizing myelopathy", "Subacute angiohypertrophic myelomalacia", "Subacute ascending necrotizing myelitis", "Subacute necrotizing myelitis (disorder)", "familial osteosclerosis with abnormalities of the nervous system and meninges"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Foix-Alajouanine syndrome", "shortest_name_length": 25}
{"curie": "UMLS:C4744985", "names": ["Advanced Gastric Large Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Gastric Large Cell Neuroendocrine Carcinoma", "shortest_name_length": 52}
{"curie": "MONDO:0030756", "names": ["STWS2", "STUVE-WIEDEMANN SYNDROME 2", "Stuve-Wiedemann syndrome 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stuve-Wiedemann syndrome 2", "shortest_name_length": 5}
{"curie": "MONDO:0013155", "names": ["MDDGB3", "congenital muscular dystrophy-POMGNT1 related", "congenital muscular dystrophy POMGNT1-related", "muscular dystrophy-dystroglycanopathy type B3", "MUSCULAR DYSTROPHY, CONGENITAL, POMGNT1-RELATED", "muscular dystrophy, congenital, POMGNT1-related", "muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 3", "muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B3", "muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B, 3", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH IMPAIRED INTELLECTUAL DEVELOPMENT), TYPE B, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B3", "shortest_name_length": 6}
{"curie": "MONDO:0018227", "names": ["McDuffie syndrome", "Mac Duffie syndrome", "anti-C1q vasculitis", "Anti-C1q vasculitis", "urticarial vasculitis", "vasculitis urticarial", "hypocomplementemic vasculitis", "Hypocomplementemic vasculitis", "Hypocomplementaemic vasculitis", "hypocomplementemic; vasculitis", "vasculitis; with hypocomplementemic", "hypocomplementemic urticarial vasculitis", "Hypocomplementemic urticarial vasculitis", "Hypocomplementaemic urticarial vasculitis", "McDuffie hypocomplementemic urticarial vasculitis", "Hypocomplementemic urticarial vasculitis (disorder)", "Mac Duffie hypocomplementemic urticarial vasculitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypocomplementemic urticarial vasculitis", "shortest_name_length": 17}
{"curie": "MONDO:0008817", "names": ["Gaci", "GACI1", "arteriopathy, occlusive infantile", "Coronary Sclerosis, Medial, of Infancy", "coronary sclerosis, medial, of infancy", "CORONARY SCLEROSIS, MEDIAL, OF INFANCY", "ENPP1 arterial calcification of infancy", "idiopathic infantile arterial calcification", "arterial calcification, idiopathic infantile", "generalized arterial calcification of infancy 1", "Generalized Arterial Calcification of Infancy 1", "ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 1", "arterial calcification, generalized, of infancy, 1", "arterial calcification, generalized, of infancy, type 1", "arterial calcification of infancy caused by mutation in ENPP1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arterial calcification, generalized, of infancy, 1", "shortest_name_length": 4}
{"curie": "UMLS:C3274522", "names": ["Surfactant Protein A Deficiency", "Surfactant Apoprotein A Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Surfactant Protein A Deficiency", "shortest_name_length": 31}
{"curie": "UMLS:C0877510", "names": ["precancerous dermatosis", "Precancerous Dermatosis", "PREMALIGNANT DERMATOSIS", "Precancerous skin lesion", "Precancerous Skin Lesion", "Cutaneous Premalignant Condition", "Cutaneous Precancerous Condition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Precancerous skin lesion", "shortest_name_length": 23}
{"curie": "MONDO:0001511", "names": ["thyrotoxic exophthalmos", "Thyrotoxic exophthalmos", "Exophthalmos thyrotoxic", "Exophthalmic thyrotoxicosis", "exophthalmic hyperthyroidism", "Thyrotoxic exophthalmos (disorder)", "exophthalmic hyperthyroidism (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyrotoxic exophthalmos", "shortest_name_length": 23}
{"curie": "MONDO:0005581", "names": ["AVL induced bursal lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AVL induced bursal lymphoma", "shortest_name_length": 27}
{"curie": "MONDO:0009343", "names": ["Hirschsprung disease polydactyly heart disease", "Hirschsprung Disease with Ulnar Polydactyly, Polysyndactyly of Big Toes, and Ventricular Septal Defect", "Hirschsprung disease with ulnar polydactyly, polysyndactyly of big toes, and ventricular septal defect", "HIRSCHSPRUNG DISEASE WITH ULNAR POLYDACTYLY, POLYSYNDACTYLY OF BIG TOES, AND VENTRICULAR SEPTAL DEFECT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hirschsprung disease with ulnar polydactyly, polysyndactyly of big toes, and ventricular septal defect", "shortest_name_length": 46}
{"curie": "UMLS:C1334997", "names": ["Non-Neoplastic Bone Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Bone Disorder", "shortest_name_length": 28}
{"curie": "UMLS:C1332216", "names": ["Systemic Anaplastic Large Cell Lymphoma", "Adult Systemic Anaplastic Large Cell Lymphoma", "Adult Systemic K-1+ Anaplastic Large Cell Lymphoma", "Adult Systemic CD30+ Anaplastic Large Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Systemic Anaplastic Large Cell Lymphoma", "shortest_name_length": 39}
{"curie": "MONDO:0008336", "names": ["Ptergyium Colli", "PTERYGIUM COLLI, ISOLATED", "Pterygium Colli, Isolated", "pterygium colli, isolated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pterygium colli, isolated", "shortest_name_length": 15}
{"curie": "MONDO:0005081", "names": ["EPH Complex", "EPH Toxemia", "eph gestosis", "Toxemia, EPH", "PREECLAMPSIA", "Preeclampsia", "preeclampsia", "EPH Toxemias", "EPH Gestosis", "PRE-ECLAMPSIA", "Pre-Eclampsia", "Toxemias, EPH", "pre-eclampsia", "pre eclampsia", "Pre-eclampsia", "Gestosis, EPH", "Pre Eclampsia", "Pregnancy Toxemia", "Pre-eclampsia NOS", "pregnancy toxemia", "Pre-eclamptic NOS", "Toxemia, Pregnancy", "PE - Pre-eclampsia", "Pregnancy Toxemias", "Pre-eclampsia, NOS", "Toxemias, Pregnancy", "Toxemia Of Pregnancy", "Toxemia of pregnancy", "Toxaemia of pregnancy", "Pre-eclampsia toxemia", "Pregnancy, Toxemia Of", "Of Pregnancy, Toxemia", "toxaemia of pregnancy", "Toxemia, preeclamptic", "Pre-eclamptic toxemia", "Pre-eclamptic toxaemia", "preeclampsia/eclampsia", "Toxemia (pre)eclampsia", "pre-eclamptic; toxemia", "Pre-eclampsia toxaemia", "toxemia; pre-eclamptic", "Toxemia Of Pregnancies", "pre-eclamptic toxaemia", "Of Pregnancies, Toxemia", "Pregnancies, Toxemia Of", "Pre-eclampsia (disorder)", "gestational hypertension", "Preeclampsia Eclampsia 1", "pregnancy; pre-eclampsia", "Unspecified pre-eclampsia", "pre-eclampsia (diagnosis)", "Preeclampsia Eclampsia 1s", "1, Preeclampsia Eclampsia", "Eclampsia 1, Preeclampsia", "1s, Preeclampsia Eclampsia", "Pre-eclamptic toxemia, NOS", "Eclampsia 1s, Preeclampsia", "Pre-eclampsia, unspecified", "Pre-eclamptic toxaemia, NOS", "PET - Pre-eclamptic toxemia", "PET - Pre-eclamptic toxaemia", "pregnancy associated hypertension", "hypertension induced by pregnancy", "Proteinuric hypertension of pregnancy", "proteinuric hypertension of pregnancy", "Edema-Proteinuria-Hypertension Gestosis", "Hypertension-Edema-Proteinuria Gestosis", "Hypertension Edema Proteinuria Gestosis", "Proteinuria-Edema-Hypertension Gestosis", "Proteinuria Edema Hypertension Gestosis", "Edema Proteinuria Hypertension Gestosis", "Gestosis, Hypertension-Edema-Proteinuria", "Gestosis, Proteinuria-Edema-Hypertension", "Gestosis, Edema-Proteinuria-Hypertension", "Unspecified pre-eclampsia, unspecified trimester", "EPH - Edema, proteinuria and hypertension of pregnancy", "EPH - Oedema, proteinuria and hypertension of pregnancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "preeclampsia", "shortest_name_length": 11}
{"curie": "UMLS:C0740375", "names": ["Incarcerated Inguinal Hernia", "INGUINAL HERNIA INCARCERATED", "Incarcerated inguinal hernia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Incarcerated inguinal hernia", "shortest_name_length": 28}
{"curie": "MONDO:0016739", "names": ["CNS yolk Sac tumor", "CNS Yolk Sac Tumor", "Yolk sac tumor of CNS", "Yolk Sac Tumor of CNS", "yolk Sac tumor of CNS", "yolk sac tumor of CNS", "Yolk Sac Tumor of the CNS", "yolk Sac tumor of the CNS", "Intracranial yolk sac tumor", "intracranial yolk sac tumor", "endodermal sinus tumor of CNS", "Endodermal sinus tumor of CNS", "intracranial endodermal sinus tumor", "Intracranial endodermal sinus tumor", "central nervous system yolk Sac tumor", "Central Nervous System Yolk Sac Tumor", "Yolk Sac Tumor of Central Nervous System", "yolk sac tumor of central nervous system", "Yolk sac tumor of central nervous system", "yolk Sac tumor of central nervous system", "Yolk sac tumour of central nervous system", "Yolk Sac Tumor of the Central Nervous System", "yolk Sac tumor of the central nervous system", "endodermal sinus tumor of central nervous system", "Endodermal sinus tumor of central nervous system", "Endodermal sinus tumour of central nervous system", "Endodermal sinus neoplasm of central nervous system", "Yolk sac tumor of central nervous system (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "yolk sac tumor of central nervous system", "shortest_name_length": 18}
{"curie": "UMLS:C0475718", "names": ["Neonatal hyperglycemia", "Neonatal Hyperglycemia", "neonatal hyperglycemia", "Neonatal hyperglycaemia", "Neonatal hyperglycemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neonatal hyperglycemia", "shortest_name_length": 22}
{"curie": "MONDO:0009340", "names": ["hexokinase deficiency hemolytic anemia", "Hexokinase Deficiency Hemolytic Anemia", "hemolytic anemia due to hexokinase deficiency", "nonspherocytic hemolytic anemia due to hexokinase deficiency", "non-spherocytic hemolytic anemia due to hexokinase deficiency", "HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY", "hemolytic anemia, nonspherocytic, due to hexokinase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-spherocytic hemolytic anemia due to hexokinase deficiency", "shortest_name_length": 38}
{"curie": "MONDO:0004523", "names": ["clear cell squamous cell skin carcinoma", "Skin Clear Cell Squamous Cell Carcinoma", "Clear Cell Squamous Cell Skin Carcinoma", "Clear cell squamous cell carcinoma of skin", "Clear Cell Squamous Cell Carcinoma of Skin", "clear cell squamous cell carcinoma of skin", "clear cell squamous cell carcinoma of the skin", "Clear Cell Squamous Cell Carcinoma of the Skin", "skin neoplasm carcinoma squamous cell clear cell", "SCC - Clear cell squamous cell carcinoma of skin", "Clear cell squamous cell carcinoma of skin (disorder)", "Clear cell squamous cell carcinoma of skin (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "clear cell squamous cell skin carcinoma", "shortest_name_length": 39}
{"curie": "UMLS:C3203360", "names": ["Suppuration", "suppuration", "Suppurative", "suppurative", "suppurations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Suppuration", "shortest_name_length": 11}
{"curie": "UMLS:C3714237", "names": ["Trifunctional Protein Deficiency, Type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Trifunctional Protein Deficiency, Type 2", "shortest_name_length": 40}
{"curie": "MONDO:0012713", "names": ["spondylometaphyseal dysplasia East African type", "spondylometaphyseal dysplasia East-African type", "Spondylometaphyseal Dysplasia, East African Type", "spondylometaphyseal dysplasia, East African type", "SPONDYLOMETAPHYSEAL DYSPLASIA, EAST AFRICAN TYPE", "Spondylometaphyseal dysplasia, east-African type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondylometaphyseal dysplasia, East African type", "shortest_name_length": 47}
{"curie": "UMLS:C1333936", "names": ["Hard Palate Adenoid Cystic Carcinoma", "Adenoid Cystic Carcinoma of Hard Palate", "Adenoid Cystic Carcinoma of the Hard Palate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hard Palate Adenoid Cystic Carcinoma", "shortest_name_length": 36}
{"curie": "UMLS:C5554972", "names": ["Locally Advanced HER2 Negative Breast Carcinoma", "Locally Advanced HER2-Negative Breast Carcinoma", "Locally Advanced HER2 Negative Breast Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced HER2-Negative Breast Carcinoma", "shortest_name_length": 47}
{"curie": "UMLS:C0345195", "names": ["Congenital jejunal stenosis", "Congenital Jejunal Stenosis", "stenosis; jejunum, congenital", "jejunum; stenosis, congenital", "Congenital stenosis of jejunum", "congenital stenosis of jejunum", "stenosis of jejunum congenital", "Congenital jejunal stenosis (disorder)", "stenosis of jejunum congenital (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital jejunal stenosis", "shortest_name_length": 27}
{"curie": "UMLS:C0349675", "names": ["Hypergranular promyelocytic leukemia", "Typical Acute Promyelocytic Leukemia", "Hypergranular promyelocytic leukaemia", "Hypergranular Acute Promyelocytic Leukemia", "acute promyelocytic leukemia, hypergranular", "Hypergranular promyelocytic leukemia (disorder)", "acute promyelocytic leukemia, hypergranular (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypergranular promyelocytic leukemia", "shortest_name_length": 36}
{"curie": "UMLS:C1335094", "names": ["Occult Lung Adenosquamous Carcinoma", "Occult Adenosquamous Cell Lung Carcinoma", "Occult Adenosquamous Cell Carcinoma of Lung", "Occult Adenosquamous Cell Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Occult Lung Adenosquamous Carcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C1828283", "names": ["Allergy, Bee", "Bee Venom Allergy", "Bee Sting Allergy", "Allergy to bee venom", "Allergy to bee venom (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Allergy to bee venom", "shortest_name_length": 12}
{"curie": "UMLS:C4521001", "names": ["Stage III Nasopharyngeal Carcinoma", "Stage III Nasopharyngeal Throat Cancer", "Stage III Nasopharyngeal Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Nasopharyngeal Carcinoma AJCC v7", "shortest_name_length": 34}
{"curie": "MONDO:0012854", "names": ["microtia with or without hearing impairment", "MICROTIA WITH OR WITHOUT HEARING IMPAIRMENT", "Microtia, Hearing Impairment, And Cleft Palate", "microtia, hearing impairment, and cleft palate", "MICROTIA, HEARING IMPAIRMENT, AND CLEFT PALATE", "microtia with or without hearing impairment (AD)", "bilateral microtia-deafness-cleft palate syndrome", "microtia, hearing impairment, and cleft palate (AR)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bilateral microtia-deafness-cleft palate syndrome", "shortest_name_length": 43}
{"curie": "MONDO:0010508", "names": ["MRX103", "XLID103", "X-linked mental retardation 103", "MENTAL RETARDATION, X-LINKED 103", "mental retardation, X-linked 103", "intellectual disability, X-linked 103", "mental retardation, X-linked type 103", "intellectual disability, X-linked type 103", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 103", "non-syndromic X-linked intellectual disability 103", "KLHL15 non-syndromic X-linked intellectual disability", "intellectual developmental disorder, X-linked 103, X-linked recessive", "non-syndromic X-linked intellectual disability caused by mutation in KLHL15"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 103", "shortest_name_length": 6}
{"curie": "MONDO:0005938", "names": ["renal tb", "Renal TB", "TB of the kidney", "RENAL TUBERCULOSIS", "renal tuberculosis", "Renal tuberculosis", "Renal Tuberculosis", "Renal Tuberculoses", "tuberculosis renal", "Tuberculoses, Renal", "Tuberculosis;kidney", "tuberculosis kidney", "kidney tuberculosis", "Tuberculosis, Renal", "KIDNEY, TUBERCULOSIS", "kidneys tuberculosis", "Kidneys--Tuberculosis", "tuberculosis of kidney", "kidney of tuberculosis", "Tuberculosis of kidney", "of kidney tuberculosis", "TB - Renal tuberculosis", "Tuberculous nephropathy", "Tuberculous pyelonephritis", "renal; tuberculous (etiology)", "kidney; tuberculous (etiology)", "Tuberculosis of kidney (disorder)", "renal; tuberculous (manifestation)", "tuberculosis of kidney (diagnosis)", "Tuberculosis of kidney, unspecified", "kidney; tuberculous (manifestation)", "Tuberculosis of kidney, unspecified examination"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal tuberculosis", "shortest_name_length": 8}
{"curie": "MONDO:0009910", "names": ["WDRTS", "Neonatal Progeroid Syndrome", "progeroid syndrome neonatal", "Neonatal progeroid syndrome", "neonatal progeroid syndrome", "progeroid syndrome, neonatal", "PROGEROID SYNDROME, NEONATAL", "Progeroid syndrome, neonatal", "WIEDEMANN-RAUTENSTRAUCH SYNDROME", "wiedemann-rautenstrauch syndrome", "Wiedemann-Rautenstrauch syndrome", "Wiedemann-Rautenstrauch Syndrome", "Wiedemann Rautenstrauch syndrome", "Wiedemann-Rautenstrauch (WR) syndrome", "neonatal pseudohydrocephalic progeroid syndrome", "Neonatal pseudo-hydrocephalic progeroid syndrome", "congenital pseudohydrocephalic progeroid syndrome", "Neonatal progeroid syndrome of Wiedemann-Rautenstrauch", "Neonatal pseudo-hydrocephalic progeroid syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wiedemann-Rautenstrauch syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0015763", "names": ["mosaic trisomy 2", "Mosaic trisomy 2", "trisomy 2 mosaicism", "Trisomy 2 mosaicism", "Mosaic trisomy type 2", "Mosaic trisomy 2 syndrome", "Mosaic trisomy chromosome 2", "Mosaic trisomy 2 syndrome (disorder)", "Mosaic trisomy 2 syndrome (diagnosis)", "anomaly of chromosome pair mosaic trisomy 2 syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mosaic trisomy 2", "shortest_name_length": 16}
{"curie": "MONDO:0032873", "names": ["RP87", "RETINITIS PIGMENTOSA 87 WITH CHOROIDAL INVOLVEMENT", "retinitis pigmentosa 87 with choroidal involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 87 with choroidal involvement", "shortest_name_length": 4}
{"curie": "MONDO:0002924", "names": ["smooth muscle cancer", "Smooth Muscle Cancer", "Cancer of Smooth Muscle", "cancer of smooth muscle", "Cancer of the Smooth Muscle", "cancer of the smooth muscle", "malignant smooth muscle tumor", "Malignant Smooth Muscle Tumor", "Malignant Smooth Muscle Neoplasm", "malignant tumor of smooth muscle", "malignant smooth muscle neoplasm", "Malignant Tumor of Smooth Muscle", "malignant tumor of Smooth Muscle", "malignant neoplasm of smooth muscle", "Malignant Neoplasm of Smooth Muscle", "Malignant Tumor of the Smooth Muscle", "malignant tumor of the smooth muscle", "Malignant Neoplasm of the Smooth Muscle", "malignant neoplasm of the smooth muscle"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "smooth muscle cancer", "shortest_name_length": 20}
{"curie": "UMLS:C3899502", "names": ["Congenital Varicella Zoster Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Varicella Zoster Infection", "shortest_name_length": 37}
{"curie": "MONDO:0030012", "names": ["DIJOS", "IDDFD", "DIETS-JONGMANS SYNDROME", "diets-jongmans syndrome", "Diets-Jongmans syndrome", "Intellectual Developmental Disorder With Distinctive Facial Dysmorphism", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH DISTINCTIVE FACIAL DYSMORPHISM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diets-Jongmans syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C5204118", "names": ["Proximal Tubulopathy without Crystals", "Light Chain Proximal Tubulopathy without Crystals"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Light Chain Proximal Tubulopathy without Crystals", "shortest_name_length": 37}
{"curie": "MONDO:0010273", "names": ["Hodgkin disease, X-linked pseudoautosomal", "HODGKIN DISEASE, X-LINKED PSEUDOAUTOSOMAL", "Hodgkin disease, X-linked Pseudoautosomal", "lymphoma, Hodgkin, X-linked pseudoautosomal", "LYMPHOMA, HODGKIN, X-LINKED PSEUDOAUTOSOMAL", "Hodgkin disease susceptibility, pseudoautosomal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphoma, Hodgkin, X-linked pseudoautosomal", "shortest_name_length": 41}
{"curie": "MONDO:0009093", "names": ["DERMATOLEUKODYSTROPHY", "Dermatoleukodystrophy", "dermatoleukodystrophy", "Cutis laxa-leukodystrophy", "Dermatoleukodystrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermatoleukodystrophy", "shortest_name_length": 21}
{"curie": "MONDO:0024648", "names": ["optic tract meningioma", "meningioma of optic tract", "Visual Pathway Meningioma", "visual pathway meningioma", "meningioma of visual pathway", "Meningioma of Visual Pathway", "meningioma of the optic tract", "optic tract meningioma (disease)", "meningioma of the visual pathway", "Meningioma of the Visual Pathway", "meningioma (disease) of optic tract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "optic tract meningioma", "shortest_name_length": 22}
{"curie": "MONDO:0019864", "names": ["Tetrasomy 21", "tetrasomy 21", "Isochromosome 21", "tetrasomy type 21", "Tetrasomy 21 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tetrasomy 21", "shortest_name_length": 12}
{"curie": "MONDO:0013813", "names": ["DYT21", "DYSTONIA 21", "dystonia 21", "dystonia type 21", "Primary dystonia 21", "Primary dystonia DYT21 type", "primary dystonia, DYT21 type", "Primary dystonia, DYT21 type", "Primary dystonia 21 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dystonia 21", "shortest_name_length": 5}
{"curie": "MONDO:0000372", "names": ["Pharyngeal Cancer Stage 0", "pharynx in situ carcinoma", "Stage 0 Pharyngeal Cancer", "Stage 0 Pharynx Carcinoma", "Pharynx Carcinoma in situ", "pharyngeal cancer stage 0", "Cancer in situ of pharynx", "stage 0 pharyngeal cancer", "pharynx carcinoma in situ", "stage 0 pharynx carcinoma", "carcinoma in situ of pharynx", "Carcinoma in situ of pharynx", "stage 0 pharyngeal carcinoma", "stage 0 carcinoma of pharynx", "Carcinoma in situ of Pharynx", "Stage 0 Pharyngeal Carcinoma", "Pharyngeal Carcinoma in situ", "Stage 0 Carcinoma of Pharynx", "pharyngeal carcinoma in situ", "PHARYNGEAL CARCINOMA IN SITU", "Stage 0 Pharyngeal Throat Cancer", "stage 0 pharyngeal throat cancer", "Stage 0 Carcinoma of the Pharynx", "carcinoma in situ of the pharynx", "stage 0 carcinoma of the pharynx", "Carcinoma in situ of the Pharynx", "Carcinoma in situ of pharynx, NOS", "Carcinoma in situ of pharynx (disorder)", "carcinoma in situ of pharynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pharynx carcinoma in situ", "shortest_name_length": 25}
{"curie": "UMLS:C1709506", "names": ["Peritoneal Laceration", "Peritoneal laceration", "Peritoneal Laceration(s)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peritoneal laceration", "shortest_name_length": 21}
{"curie": "UMLS:C4688353", "names": ["Unresectable Craniopharyngioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Craniopharyngioma", "shortest_name_length": 30}
{"curie": "MONDO:0016357", "names": ["Kozlowski-Tsuruta syndrome", "dysplastic cortical hyperostosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dysplastic cortical hyperostosis", "shortest_name_length": 26}
{"curie": "UMLS:C1332964", "names": ["Clear Cell Sarcoma of Soft Tissue", "Pediatric Clear Cell Sarcoma of Soft Parts", "Childhood Clear Cell Sarcoma of Soft Parts", "Childhood Clear Cell Sarcoma of Soft Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Clear Cell Sarcoma of Soft Parts", "shortest_name_length": 33}
{"curie": "UMLS:C0677697", "names": ["Stage II Lymphoblastic Lymphoma", "contiguous adult lymphoblastic lymphoma stage II", "adult contiguous lymphoblastic lymphoma stage II", "Contiguous Adult Stage II Lymphoblastic Lymphoma", "Stage II Contiguous Adult Lymphoblastic Lymphoma", "stage II contiguous adult lymphoblastic lymphoma", "Adult Contiguous Lymphoblastic Lymphoma Stage II", "contiguous adult stage II lymphoblastic lymphoma", "contiguous stage II adult lymphoblastic lymphoma", "Contiguous Adult Lymphoblastic Lymphoma Stage II", "stage II contiguous adult precursor lymphoblastic lymphoma", "Stage II Contiguous Adult Precursor Lymphoblastic Lymphoma", "Ann Arbor Stage II Contiguous Adult Lymphoblastic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage II Contiguous Adult Lymphoblastic Lymphoma", "shortest_name_length": 31}
{"curie": "MONDO:0014541", "names": ["TEMPLE syndrome", "Temple syndrome", "TEMPLE SYNDROME", "Temple Syndrome", "mUPD14 Syndrome", "mUPD14 syndrome", "Temple syndrome (disorder)", "UNIPARENTAL DISOMY, MATERNAL, CHROMOSOME 14", "uniparental disomy, maternal, chromosome 14", "Maternal uniparental disomy of chromosome 14", "Maternal Uniparental Disomy Chromosome 14 Syndrome", "maternal uniparental disomy chromosome 14 syndrome", "Maternal uniparental disomy of chromosome 14 (disorder)", "motor developmental delay due to 14q32.2 paternally expressed gene defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "motor developmental delay due to 14q32.2 paternally expressed gene defect", "shortest_name_length": 15}
{"curie": "MONDO:0021043", "names": ["Mixed Tumor", "mixed tumor", "Mixed Neoplasm", "mixed neoplasm", "Complex and Mixed Neoplasms", "Neoplasms, Complex and Mixed"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed neoplasm", "shortest_name_length": 11}
{"curie": "UMLS:C5667239", "names": ["Refractory Metastatic Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Metastatic Melanoma", "shortest_name_length": 30}
{"curie": "UMLS:C0525047", "names": ["Sexual and Gender Disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sexual and Gender Disorders", "shortest_name_length": 27}
{"curie": "MONDO:0011438", "names": ["acne", "Acne", "Zits", "ACNE", "Acnes", "Acne NOS", "Acne, NOS", "acne, adult", "Common acne", "Breaking out", "Acne;vulgaris", "Acne vulgaris", "Acne Vulgaris", "acne vulgaris", "ACNE VULGARIS", "vulgaris; acne", "frontalis acne", "acne; vulgaris", "acne (disease)", "acne frontalis", "Acne frontalis", "Acne, vulgaris", "acne; frontalis", "Acne, frontalis", "Acne (disorder)", "frontalis; acne", "acne (diagnosis)", "Acne, unspecified", "acne varioliformis", "Acne varioliformis", "varioliformis; acne", "acne; varioliformis", "Acne vulgaris (disorder)", "acne vulgaris (diagnosis)", "Acne varioliformis (disorder)", "acne varioliformis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acne", "shortest_name_length": 4}
{"curie": "UMLS:C0877337", "names": ["bleed tongue", "tongue bleed", "bleeding tongue", "Tongue bleeding", "Bleeding;tongue", "tongue bleeding", "Tongue hemorrhage", "hemorrhage; tongue", "Tongue hemorrhagic", "tongue; hemorrhage", "Tongue haemorrhage", "tongue haemorrhage", "bleeding of tongue", "Hemorrhage of tongue", "Bleeding from tongue", "bleeding from the tongue", "Hemorrhage of tongue (finding)", "bleeding of tongue (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemorrhage of tongue", "shortest_name_length": 12}
{"curie": "MONDO:0016042", "names": ["late-onset isolated ACTH deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "late-onset isolated ACTH deficiency", "shortest_name_length": 35}
{"curie": "MONDO:0009722", "names": ["NAM", "MYPBB", "STAC3 disorder", "congenital myopathy 13", "Native American myopathy", "NATIVE AMERICAN MYOPATHY", "Bailey-Bloch congenital myopathy", "myopathy, congenital, baily-bloch", "MYOPATHY, CONGENITAL, BAILEY-BLOCH", "Native American myopathy (disorder)", "congenital myopathy cleft palate and malignant hyperthermia", "Congenital myopathy cleft palate and malignant hyperthermia", "congenital myopathy - cleft palate - malignant hyperthermia", "Congenital myopathy-cleft palate-malignant hyperthermia syndrome", "congenital myopathy-cleft palate-malignant hyperthermia syndrome", "Myopathy, Congenital, With Cleft Palate And Malignant Hyperthermia", "Congenital myopathy, cleft palate. malignant hyperthermia syndrome", "myopathy, congenital, with cleft palate and malignant hyperthermia", "MYOPATHY, CONGENITAL, WITH MYOPATHIC FACIES, SCOLIOSIS, AND MALIGNANT HYPERTHERMIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bailey-Bloch congenital myopathy", "shortest_name_length": 3}
{"curie": "UMLS:C0239062", "names": ["Perioral edema", "Perioral oedema", "CIRCUMORAL EDEMA", "Circumoral edema", "Circumoral oedema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Circumoral edema", "shortest_name_length": 14}
{"curie": "MONDO:0009287", "names": ["GSD1", "GSDIa", "GSD1A", "GSD Ia", "GSD type 1a", "Von Gierke Disease", "Von Gierke disease", "VON GIERKE DISEASE", "glycogenosis type Ia", "G6P deficiency type 1a", "Hepatorenal glycogenosis", "HEPATORENAL GLYCOGENOSIS", "Hepatorenal Glycogenosis", "hepatorenal glycogenosis", "GLYCOGEN STORAGE DISEASE I", "glycogen storage disease 1", "glycogen storage disease Ia", "GLYCOGEN STORAGE DISEASE Ia", "glycogen storage disease 1A", "G6PC glycogen storage disease", "glycogen storage disease type Ia", "GLUCOSE-6-PHOSPHATASE DEFICIENCY", "Glycogen storage disease type Ia", "Glucose-6 Phosphatase Deficiency", "glucose-6-phosphatase deficiency", "glycogen storage disease type 1a", "Glycogen storage disease type IA", "Glycogen Storage Disease Type Ia", "GSD due to G6P deficiency type Ia", "GSD due to G6P deficiency type 1a", "von Gierke's disease (GSD type IA)", "Glycogen storage disease type Ia (disorder)", "Hepatorenal form of glycogen storage disease", "hepatorenal form of glycogen storage disease", "HEPATORENAL FORM OF GLYCOGEN STORAGE DISEASE", "von Gierke's disease (GSD type IA) (diagnosis)", "glycogen storage disease caused by mutation in G6PC", "glycogen storage disease due to G6P deficiency type Ia", "glucose-6-phosphatase deficiency glycogen storage disease", "glycogenosis due to glucose-6-phosphatase deficiency type 1a", "glycogenosis due to glucose-6-phosphatase deficiency type Ia", "glycogen storage disease due to glucose-6-phosphatase deficiency type IA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease due to glucose-6-phosphatase deficiency type IA", "shortest_name_length": 4}
{"curie": "UMLS:C4683644", "names": ["Adult Non-Hodgkin Lymphoma by Ann Arbor Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Non-Hodgkin Lymphoma by Ann Arbor Stage", "shortest_name_length": 45}
{"curie": "MONDO:0004801", "names": ["Unilateral hypoactive labyrinth", "unilateral hypoactive labyrinth", "Hypoactive labyrinth, unilateral", "unilateral hypoactive labyrinth (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "unilateral hypoactive labyrinth", "shortest_name_length": 31}
{"curie": "UMLS:C0270192", "names": ["Perinatal Subarachnoid Hemorrhage", "Perinatal subarachnoid hemorrhage", "Hemorrhage, Perinatal Subarachnoid", "Perinatal subarachnoid haemorrhage", "Perinatal Subarachnoid Hemorrhages", "Subarachnoid Hemorrhage, Perinatal", "Hemorrhages, Perinatal Subarachnoid", "Subarachnoid Hemorrhages, Perinatal", "Perinatal intracranial subarachnoid hemorrhage", "Perinatal intracranial subarachnoid haemorrhage", "Subarachnoid hemorrhage from any perinatal cause", "Subarachnoid haemorrhage from any perinatal cause", "Perinatal intracranial subarachnoid hemorrhage (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perinatal Subarachnoid Hemorrhage", "shortest_name_length": 33}
{"curie": "UMLS:C0332687", "names": ["SECOND DEGREE BURN", "burn degree second", "Second-Degree Burn", "second degree burn", "burn second degree", "Second degree burn", "Second Degree Burn", "Burns second degree", "burns degree second", "second degree burns", "Second degree burns", "partial thickness burn", "Partial thickness burn", "burns partial thickness", "Second degree burn injury", "PT - Partial thickness burn", "second degree burns (diagnosis)", "Burn blister with epidermal loss", "Partial thickness burn (disorder)", "Partial thickness (Second Degree) Burn", "partial thickness (second degree) burns", "Second degree burn injury (morphologic abnormality)", "Blisters with epidermal loss due to burn, unspecified site", "Blisters, epidermal loss [second degree], unspecified site", "Blisters with epidermal loss due to second degree burn, unspecified site", "Blisters with epidermal loss due to burn [second degree], unspecified site", "Blisters with epidermal loss due to burn (second degree), unspecified site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Partial thickness burn", "shortest_name_length": 18}
{"curie": "MONDO:0019981", "names": ["unilateral MCDK", "unilateral multicystic renal dysplasia", "unilateral multicystic dysplastic kidney"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "unilateral multicystic dysplastic kidney", "shortest_name_length": 15}
{"curie": "MONDO:0013937", "names": ["PBD6B", "Peroxisome Biogenesis Disorder 6B", "peroxisome biogenesis disorder 6B", "PEROXISOME BIOGENESIS DISORDER 6B", "peroxisome biogenesis disorder type 6B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder 6B", "shortest_name_length": 5}
{"curie": "UMLS:C0037448", "names": ["Socialized Conduct Disorder", "Socialized conduct disorder", "socialized conduct disorder", "Socialised conduct disorder", "Socialized behavior disorder", "Socialized behaviour disorder", "Socialised behaviour disorder", "Conduct disorder - socialised", "Conduct disorder - socialized", "behavioral disorder; socialized", "socialized; behavioral disorder", "Socialized behavior disorder (disorder)", "socialized conduct disorder (diagnosis)", "Socialized conduct disorder, unspecified", "Socialized conduct disorder, unspecified degree"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Socialized behavior disorder", "shortest_name_length": 27}
{"curie": "MONDO:0006923", "names": ["Bacillaceae infection", "Bacillaceae Infection", "Bacillaceae Infections", "infection, Bacillaceae", "Infection, Bacillaceae", "Infections, Bacillaceae", "infections, Bacillaceae", "Bacillaceae infectious disease", "Bacillaceae disease or disorder", "primary Bacillaceae infectious disease", "Bacillaceae caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bacillaceae infectious disease", "shortest_name_length": 21}
{"curie": "MONDO:0027766", "names": ["Generalized Lipodystrophy", "Generalised lipodystrophy", "Generalized lipodystrophy", "generalized lipodystrophy", "Lipodystrophy, generalized", "Lipodystrophy, generalised", "complete generalized lipodystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "generalized lipodystrophy", "shortest_name_length": 25}
{"curie": "MONDO:0001328", "names": ["RTH", "GTHR", "RTSH", "TSH resistance", "Refetoff Syndrome", "Refetoff syndrome", "Syndrome, Refetoff", "THYROTROPIN RESISTANCE", "RESISTANCE TO THYROTROPIN", "resistance to thyrotropin", "Resistance to thyrotropin", "hormone resistance thyroid", "thyroid hormone resistance", "Thyroid hormone resistance", "Thyroid Hormone Resistance", "Resistance, Thyroid Hormone", "hormone resistances thyroid", "Hormone Resistance, Thyroid", "Refetoff syndrome (disorder)", "Resistance to thyroid hormone", "Thyroid hormone receptor defect", "Refetoff DeWind DeGroot Syndrome", "Thyroid hormone unresponsiveness", "Refetoff-DeWind-DeGroot Syndrome", "Syndrome, Refetoff-DeWind-DeGroot", "General resistance to thyrotropin", "thyroid hormone resistance syndrome", "Thyroid Hormone Resistance Syndrome", "Thyroid hormone resistance syndrome", "thyroid hormone responsiveness defect", "Thyroid hormone responsiveness defect", "generalized thyroid hormone resistance", "Generalized Thyroid Hormone Resistance", "Generalized thyroid hormone resistance", "Generalised thyroid hormone resistance", "Impaired sensitivity to thyroid hormone", "THYROID HORMONE RESISTANCE, GENERALIZED", "Generalised resistance to thyroid hormone", "resistance to thyroid stimulating hormone", "Generalized Resistance to Thyroid Hormone", "Resistance to thyroid stimulating hormone", "generalized resistance to thyroid hormone", "Generalized resistance to thyroid hormone", "Congenital unresponsiveness to thyrotropin", "End-organ unresponsiveness to thyroid hormone", "Thyroid hormone resistance syndrome (disorder)", "Thyroid hormone responsiveness defect (disorder)", "Unresponsiveness of thyroid gland to thyrotropin", "Generalized thyroid hormone resistance (disorder)", "Hypothyroidism due to thyroid insensitivity to TSH", "generalized resistance to thyroid hormone (diagnosis)", "Elevated serum levels of free thyroid hormone with nonsuppressed TSH"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid hormone resistance syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0000127", "names": ["GPHYSD", "geleophysic dwarfism", "Geleophysic dwarfism", "Geleophysic dysplasia", "geleophysic dysplasia", "focal mucopolysaccharidosis", "geleophysic dwarfism syndrome", "Geleophysic dwarfism syndrome", "Geleophysic dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "geleophysic dysplasia", "shortest_name_length": 6}
{"curie": "MONDO:0001837", "names": ["SALPINGITIS GONOCOCCAL ACUTE", "Gonococcal salpingitis acute", "Salpingitis gonococcal acute", "Acute gonococcal salpingitis", "acute gonococcal salpingitis", "gonococcal salpingitis, acute", "Acute gonococcal salpingitis (disorder)", "acute gonococcal salpingitis (diagnosis)", "Gonococcal salpingitis, specified as acute", "gonococcal salpingitis, specified as acute"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute gonococcal salpingitis", "shortest_name_length": 28}
{"curie": "UMLS:C1333605", "names": ["Femoral Hernia with Obstruction without Mention of Gangrene"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Femoral Hernia with Obstruction without Mention of Gangrene", "shortest_name_length": 59}
{"curie": "UMLS:C4744617", "names": ["Localized Gastric Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized Gastric Carcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C3544179", "names": ["Accidental Drug Ingestion", "Accidental ingestion of drug", "Accidental Medicine Ingestion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Accidental ingestion of drug", "shortest_name_length": 25}
{"curie": "UMLS:C5419209", "names": ["Unresectable Endometrial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Endometrial Carcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0007303", "names": ["Costa colli", "Cervical Rib", "Cervical rib", "cervical rib", "CERVICAL RIB", "rib; cervical", "Cervical Ribs", "cervical; rib", "Rib, Cervical", "Cervical ribs", "cervical ribs", "Ribs, Cervical", "Costa cervicalis", "rib; cervical rib", "cervical rib; rib", "cervical rib disease", "cervical rib syndrome", "Cervical rib syndrome", "Cervical Rib Syndrome", "Syndrome, Cervical Rib", "Cervical Rib Syndromes", "Syndromes, Cervical Rib", "cervical; syndrome, rib", "syndrome; cervical, rib", "Cervical rib (disorder)", "cervical rib (diagnosis)", "Anomalous Cervical Rib Syndrome", "cervical rib syndrome (diagnosis)", "Supernumerary rib in cervical region", "Supernumerary rib in the cervical region", "Arterial thoracic outlet syndrome due to cervical rib", "Arterial thoracic outlet syndrome due to cervical rib (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical rib disease", "shortest_name_length": 11}
{"curie": "MONDO:0002335", "names": ["CIDP", "chronic inflammatory demyelinating polyneuritis", "Chronic Inflammatory Demyelinating Polyneuritis", "chronic inflammatory demyelinating polyneuropathy", "Chronic Inflammatory Demyelinating Polyneuropathy", "Chronic Inflammatory Demyelinating Polyradiculoneuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic inflammatory demyelinating polyneuritis", "shortest_name_length": 4}
{"curie": "UMLS:C5418893", "names": ["Advanced Ovarian Clear Cell Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Ovarian Clear Cell Adenocarcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0009596", "names": ["METAPHYSEAL CHONDRODYSPLASIA, PENA TYPE", "Metaphyseal Chondrodysplasia, Pena Type", "metaphyseal chondrodysplasia, Pena type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metaphyseal chondrodysplasia, Pena type", "shortest_name_length": 39}
{"curie": "MONDO:0003266", "names": ["ependymal tumor", "Ependymal tumor", "Ependymal Tumor", "ependymal tumors", "ependymomal tumor", "ependymal neoplasm", "Ependymal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ependymal tumor", "shortest_name_length": 15}
{"curie": "UMLS:C5203000", "names": ["Recurrent Oligodendroglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Oligodendroglioma", "shortest_name_length": 27}
{"curie": "UMLS:C3899670", "names": ["Anaplastic Hemispheric Astrocytoma", "Childhood Cerebral Anaplastic Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Cerebral Anaplastic Astrocytoma", "shortest_name_length": 34}
{"curie": "MONDO:0005669", "names": ["Black Piedra", "black piedra", "Black piedra", "black; piedra", "Piedra, Black", "Black Piedras", "piedra; black", "Piedras, Black", "Black piedra (disorder)", "black piedra (diagnosis)", "Piedraia hortae; infection", "infection; Piedraia hortae", "Piedra due to Piedraia hortae"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "black piedra", "shortest_name_length": 12}
{"curie": "MONDO:0015540", "names": ["HLH", "FHL", "Hemophagocytic Disorder", "hemophagocytic syndrome", "hemophagocytic disorder", "Hemophagocytic Syndrome", "Hemophagocytic syndrome", "haemophagocytic syndrome", "syndrome; hemophagocytic", "hemophagocytic; syndrome", "Hemophagocytic Syndromes", "Hemophagocytic syndromes", "Haemophagocytic syndrome", "hemophagocytic syndromes", "haemophagocytic syndromes", "familial histiocytic reticulosis", "hemophagocytic lymphohistiocytosis", "Hemophagocytic Lymphohistiocytosis", "Hemophagocytic Lymphohistiocytoses", "Hemophagocytic lymphohistiocytosis", "Lymphohistiocytosis, Hemophagocytic", "Lymphohistiocytoses, Hemophagocytic", "Haemophagocytic lymphohistiocytosis", "hemophagocytic syndrome (diagnosis)", "lymphohistiocytosis; hemophagocytic", "Hyperinflammatory lymphohistiocytosis", "familial hemophagocytic lymphohistiocytosis", "Hemophagocytic lymphohistiocytosis (disorder)", "familial erythrophagocytic lymphohistiocytosis", "hemophagocytic lymphohistiocytosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemophagocytic syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0005849", "names": ["allergy milk", "milk allergy", "Milk allergy", "Milk Allergy", "Allergy, Milk", "milk allergies", "Milk Allergies", "Milk allergies", "allergies milk", "milk food allergy", "allergies food milk", "FOOD ALLERGY TO MILK", "milk hypersensitivity", "Milk Hypersensitivity", "Hypersensitivity, Milk", "milk allergic reaction", "Milk Hypersensitivities", "FOOD ALLERGY TO MILK PRODUCT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "milk allergic reaction", "shortest_name_length": 12}
{"curie": "UMLS:C0497209", "names": ["Conjunctivitis infective", "Infective conjunctivitis", "conjunctivitis infectious", "Infectious conjunctivitis", "infectious conjunctivitis", "Conjunctivitis;infectious", "Infectious Conjunctivitis", "Conjunctivitis infectious", "CONJUNCTIVITIS INFECTIOUS", "Infective conjunctivitis (disorder)", "Infective conjunctivitis (diagnosis)", "infectious; conjunctivitis (etiology)", "infectious; conjunctivitis (manifestation)", "conjunctivitis; infectious disease (etiology)", "conjunctivitis; infectious disease (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infective conjunctivitis", "shortest_name_length": 24}
{"curie": "MONDO:0011214", "names": ["PFIC3", "MDR3 DEFICIENCY", "MDR3 deficiency", "MDR3 Deficiency", "Mdr3 deficiency", "Abcb4-Related Intrahepatic Cholestasis", "Low gamma-GT Familial Intrahepatic Cholestasis", "progressive familial intrahepatic cholestasis 3", "CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 3", "cholestasis, progressive familial intrahepatic 3", "Cholestasis, progressive familial intrahepatic 3", "cholestasis, progressive familial intrahepatic, 3", "CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 3", "Cholestasis, Progressive Familial Intrahepatic, 3", "ABCB4 progressive familial intrahepatic cholestasis", "Progressive familial intrahepatic cholestasis type 3", "progressive familial intrahepatic cholestasis type 3", "cholestasis, progressive familial intrahepatic, type 3", "Progressive Familial Intrahepatic Cholestasis 3 (PFIC3)", "Progressive Familial Intrahepatic Cholestasis 3 (PFIC 3)", "PFIC3 Progressive familial intrahepatic cholestasis type 3", "Progressive familial intrahepatic cholestasis type 3 (disorder)", "progressive familial intrahepatic cholestasis type 3 (diagnosis)", "progressive familial intrahepatic cholestasis caused by mutation in ABCB4", "progressive familial intrahepatic cholestasis with elevated serum gama-glutamyltransferase", "progressive familial intrahepatic cholestasis with elevated serum gamma-glutamyltransferase", "Progressive familial intrahepatic cholestasis with elevated serum gamma-glutamyltransferase", "CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, WITH ELEVATED SERUM GAMMA-GLUTAMYLTRANSFERASE", "Cholestasis, Progressive Familial Intrahepatic, with Elevated Serum Gamma-Glutamyltransferase", "cholestasis, progressive familial intrahepatic, with elevated serum gamma-glutamyltransferase"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive familial intrahepatic cholestasis type 3", "shortest_name_length": 5}
{"curie": "UMLS:C4725813", "names": ["Refractory Malignant Soft Tissue Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Malignant Soft Tissue Neoplasm", "shortest_name_length": 41}
{"curie": "MONDO:0006554", "names": ["annulare granuloma", "granuloma annulare", "Granuloma annulare", "GRANULOMA ANNULARE", "Granuloma Annulare", "Granulome annulare", "granuloma; annulare", "annulare; granuloma", "Necrobiotic papulosis", "GA - Granuloma annulare", "GA - granuloma annulare", "Granuloma annulare (disorder)", "granuloma annulare (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "granuloma annulare", "shortest_name_length": 18}
{"curie": "UMLS:C4683613", "names": ["Lugano Classification Stage III Adult Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage III Adult Hodgkin Lymphoma AJCC v8", "shortest_name_length": 62}
{"curie": "UMLS:C1563054", "names": ["Dapsone resistant leprosy", "Dapsone resistant leprosy (disorder)", "Dapsone resistant mycobacterium leprae", "Diaminodiphenylsulfone resistant leprosy", "Diaminodiphenylsulphone resistant leprosy", "Dapsone resistant mycobacterium leprae disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dapsone resistant mycobacterium leprae disease", "shortest_name_length": 25}
{"curie": "MONDO:0010341", "names": ["AUTSX2", "X-linked mental retardation", "x-linked mental retardation", "X-Linked Mental Retardation", "x linked mental retardation", "mental retardation x linked", "X Linked Mental Retardation", "MENTAL RETARDATION, X-LINKED", "Mental Retardation, X Linked", "Mental Retardation, X-Linked", "Retardation, X-Linked Mental", "mental retardation, X-linked", "X-Linked Mental Retardations", "intellectual disability, X-linked", "susceptibility to X-linked autism 2", "X-Linked Mental Retardation Syndromes", "AUTISM, SUSCEPTIBILITY TO, X-LINKED 2", "autism, susceptibility to, X-linked 2", "X Linked Mental Retardation Syndromes", "X Linked Mental Retardation Disorders", "X-Linked Mental Retardation Disorders", "autism, susceptibility to, X-linked type 2", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED", "AUTISM, X-LINKED, SUSCEPTIBILITY TO, 2 (finding)", "autism susceptibility, X-linked 2, isolated cases, X-linked", "intellectual developmental disorder, X-linked, Isolated cases, X-linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autism, susceptibility to, X-linked 2", "shortest_name_length": 6}
{"curie": "MONDO:0017357", "names": ["transient hyperammonemia of the newborn"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transient hyperammonemia of the newborn", "shortest_name_length": 39}
{"curie": "UMLS:C0278987", "names": ["stage IV NSCLC", "Stage IV NSCLC", "NSCLC, stage IV", "NSCLC, metastatic", "non-oat cell lung cancer, stage IV", "stage IV nonsmall cell lung cancer", "nonsmall cell lung cancer, stage IV", "lung cancer, non-oat cell, stage IV", "Lung cancer non-small cell stage IV", "stage IV non-small cell lung cancer", "Non-small cell lung cancer stage IV", "Stage IV Non-Small Cell Lung Cancer", "non-small cell lung cancer, stage IV", "non-oat cell lung cancer, metastatic", "metastatic nonsmall cell lung cancer", "lung cancer, nonsmall cell, stage IV", "Stage IV Non-Oat Cell Lung Carcinoma", "Non-small cell lung cancer metastatic", "lung cancer, non-oat cell, metastatic", "nonsmall cell lung cancer, metastatic", "Metastatic non-small cell lung cancer", "non-small cell lung cancer metastatic", "LUNG CANCER NON SMALL CELL METASTATIC", "lung cancer, nonsmall cell, metastatic", "Stage IV Non-Small Cell Lung Carcinoma", "Stage IV Non-Oat Cell Carcinoma of Lung", "Stage IV Non-Small Cell Carcinoma of Lung", "Stage IV Lung Non-Small Cell Cancer AJCC v7", "Stage IV Non-Small Cell Lung Cancer AJCC v7", "Stage IV Non-Oat Cell Carcinoma of the Lung", "Stage IV Non-Small Cell Carcinoma of the Lung", "Metastatic NSCLC - non-small cell lung cancer", "Metastatic non-small cell lung cancer (disorder)", "Metastatic non-small cell lung cancer (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic non-small cell lung cancer", "shortest_name_length": 14}
{"curie": "MONDO:0021033", "names": ["Herpes zoster dermatitis", "Herpes Zoster Dermatitis", "herpes zoster dermatitis", "Herpes zoster dermatitis (disorder)", "herpes zoster dermatitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "herpes zoster dermatitis", "shortest_name_length": 24}
{"curie": "MONDO:0018218", "names": ["autosomal recessive cerebral atrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive cerebral atrophy", "shortest_name_length": 36}
{"curie": "MONDO:0011615", "names": ["Bdet", "BDET", "East Texas bleeding disorder", "BLEEDING DISORDER, EAST TEXAS TYPE", "Bleeding Disorder, East Texas Type", "bleeding disorder, EAST Texas type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "East Texas bleeding disorder", "shortest_name_length": 4}
{"curie": "UMLS:C0030793", "names": ["pelvi tumors", "PELVIS TUMOR", "Pelvic tumor", "pelvic tumor", "pelvic tumour", "pelvic tumors", "pelvis tumors", "Pelvic tumour", "Pelvis--Tumors", "Tumor of pelvis", "pelvis neoplasm", "pelvic neoplasm", "Pelvis Neoplasm", "tumor of pelvis", "Pelvic Neoplasm", "Pelvic neoplasm", "Pelvic Neoplasms", "Pelvis Neoplasms", "Neoplasm, Pelvic", "Tumour of pelvis", "pelvic neoplasms", "Neoplasm, Pelvis", "Neoplasms, Pelvic", "Neoplasms, Pelvis", "Neoplasm of pelvis", "neoplasm of pelvis", "Neoplasms of Pelvis", "Pelvic neoplasm NOS", "Neoplasm of pelvis (disorder)", "neoplasm of pelvis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pelvic Neoplasms", "shortest_name_length": 12}
{"curie": "MONDO:0032736", "names": ["MECREN", "metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression", "METABOLIC CRISES, RECURRENT, WITH VARIABLE ENCEPHALOMYOPATHIC FEATURES AND NEUROLOGIC REGRESSION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression", "shortest_name_length": 6}
{"curie": "UMLS:C3898097", "names": ["Ophthalmologic Complication", "ophthalmologic complications"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ophthalmologic Complication", "shortest_name_length": 27}
{"curie": "MONDO:0008630", "names": ["BAIPRCK", "atony of urinary bladder", "URINARY BLADDER, ATONY OF", "urinary bladder, atony of", "BLADDER DYSFUNCTION, AUTONOMIC, WITH IMPAIRED PUPILLARY REFLEX AND SECONDARY CAKUT", "bladder dysfunction, autonomic, with impaired pupillary reflex and secondary CAKUT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urinary bladder, atony of", "shortest_name_length": 7}
{"curie": "DOID:1233", "names": ["cross dress", "Transvestism", "transvestism", "cross dresser", "Transvestisms", "Cross-dresser", "transvestitism", "Cross-dressing", "Transvestitism", "cross dressing", "cross-dressing", "Transvestic Fetishism", "fetishism transvestic", "Transvestic fetishism", "Simple cross-dressing", "transvestic fetishism", "Dual-role transvestism", "dual-role transvestism", "transvestic; fetishism", "fetishism; transvestic", "Dual role transvestism", "Transvestic Fetishisms", "Fetishism, Transvestic", "Fetishisms, Transvestic", "Fetishistic transvestism", "Cross-dressing (finding)", "fetishistic; transvestism", "transvestism; fetishistic", "Fetishistic cross-dressing", "sexual; deviation, transvestism", "deviation; sexual, transvestism", "Dual-role transvestism (finding)", "dual-role transvestism (symptom)", "transvestic fetishism (diagnosis)", "Fetishistic transvestism (disorder)", "transvestic fetishism or transvestism", "deviation; sexual, fetishism, fetishistic, transvestism", "sexual; deviation, fetishism, fetishistic, transvestism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transvestism", "shortest_name_length": 11}
{"curie": "UMLS:C4727002", "names": ["Chronic Hemolysis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic Hemolysis", "shortest_name_length": 17}
{"curie": "UMLS:C2826055", "names": ["Mixed phenotype acute leukemia T/myeloid", "Mixed phenotype acute leukaemia T/myeloid", "Mixed phenotype acute leukemia, T/myeloid, NOS", "Mixed Phenotype Acute Leukemia, T/Myeloid, NOS", "Mixed Phenotype Acute Leukemia, T/Myeloid, Not Otherwise Specified", "Mixed phenotype acute leukaemia with myeloid and T-cell lymphoid pheotypes", "Mixed phenotype acute leukemia with myeloid and T-cell lymphoid phenotypes", "Mixed phenotype acute leukemia with myeloid and T-cell lymphoid phenotypes (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mixed phenotype acute leukemia T/myeloid", "shortest_name_length": 40}
{"curie": "MONDO:0011443", "names": ["FEB4", "familial febrile seizures 4", "febrile seizures, familial, 4", "FEBRILE SEIZURES, FAMILIAL, 4", "Seizures, Familial Febrile, 4", "familial febrile convulsions 4", "Febrile Convulsions, Familial, 4", "Convulsions, Familial Febrile, 4", "FEBRILE CONVULSIONS, FAMILIAL, 4", "CONVULSIONS, FAMILIAL FEBRILE, 4", "convulsions, familial febrile, 4", "ADGRV1 febrile seizures, familial", "febrile seizures, familial, type 4", "febrile seizures, familial caused by mutation in ADGRV1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "febrile seizures, familial, 4", "shortest_name_length": 4}
{"curie": "UMLS:C5555122", "names": ["Aggressive T-Cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aggressive T-Cell Non-Hodgkin Lymphoma", "shortest_name_length": 38}
{"curie": "MONDO:0003045", "names": ["anal gland neoplasm", "Anal Gland Neoplasm", "Anal Gland Neoplasms", "Neoplasm, Anal Gland", "Neoplasms, Anal Gland", "Perianal Gland Neoplasm", "Perianal Gland Neoplasms", "Neoplasm, Perianal Gland", "gland of anal canal tumor", "Neoplasms, Perianal Gland", "Circumanal Gland Neoplasm", "Circumanal Gland Neoplasms", "Neoplasm, Circumanal Gland", "Neoplasms, Circumanal Gland", "gland of anal canal neoplasm", "tumor of gland of anal canal", "neoplasm of gland of anal canal", "gland of anal canal neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anal gland neoplasm", "shortest_name_length": 19}
{"curie": "UMLS:C1262760", "names": ["Hepatitis drug-induced", "drug induced hepatitis", "drug-induced hepatitis", "hepatitis drug induced", "Drug Induced Hepatitis", "HEPATITIS DRUG INDUCED", "Drug-Induced Hepatitis", "Drug-induced hepatitis", "drug hepatitis induced", "Hepatitis, Drug-Induced", "Hepatitis, Drug Induced", "Drug-Induced Hepatitides", "Hepatitides, Drug-Induced", "Drug-induced hepatitis (disorder)", "drug-induced hepatitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatitis, Drug-Induced", "shortest_name_length": 22}
{"curie": "UMLS:C2732618", "names": ["SSP", "SSA", "SSA/P", "Sessile Serrated Polyp", "Sessile serrated polyp", "Serrated Adenoma Type I", "Sessile Serrated Adenoma", "Sessile serrated adenoma", "Serrated Lesions and Polyps", "Sessile Serrated Adenoma/Polyp", "Sessile serrated adenoma/polyp", "Sessile Serrated Polyp/Adenoma", "Serrated Polyp with Abnormal Proliferation", "Sessile serrated adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sessile Serrated Adenoma/Polyp", "shortest_name_length": 3}
{"curie": "MONDO:0022432", "names": ["alves Castelo dos Santos syndrome", "Alves Castelo dos Santos syndrome", "Ectodermal dysplasia syndrome of hypotrichosis, onychodysplasia, hyperkeratosis, kyphoscoliosis, and cataract", "ectodermal dysplasia syndrome of hypotrichosis, onychodysplasia, hyperkeratosis, kyphoscoliosis, and cataract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alves Castelo dos Santos syndrome", "shortest_name_length": 33}
{"curie": "UMLS:C0520563", "names": ["Toxic intestinal dilatation", "Toxic dilatation of intestine", "Toxic dilatation of intestine (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Toxic dilatation of intestine", "shortest_name_length": 27}
{"curie": "MONDO:0014130", "names": ["DDD2", "Dowling-Degos disease 2", "DOWLING-DEGOS DISEASE 2", "POFUT1 Dowling-Degos disease", "Dowling-Degos disease type 2", "Dowling-Degos disease caused by mutation in POFUT1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dowling-Degos disease 2", "shortest_name_length": 4}
{"curie": "MONDO:0001504", "names": ["Fetish", "fetish", "Fetishism", "fetishism", "sexual fetishism", "Sexual Fetishism", "fetishisms sexual", "Fetishistic disorder", "Fetishism (disorder)", "Psychiatric Fetishism", "Fetishism, Psychiatric", "Fetishism (Psychiatric)", "Fetishistic disorder (diagnosis)", "deviation; sexual, fetishism, fetishistic", "sexual; deviation, fetishism, fetishistic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fetishism", "shortest_name_length": 6}
{"curie": "UMLS:C0751824", "names": ["Sagittal Sinus Thrombophlebitis", "Sinus Thrombophlebitis, Sagittal", "Thrombophlebitis, Sagittal Sinus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sagittal Sinus Thrombophlebitis", "shortest_name_length": 31}
{"curie": "UMLS:C4724968", "names": ["Refractory Myxoid Liposarcoma", "Refractory Myxoid/Round Cell Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Myxoid Liposarcoma", "shortest_name_length": 29}
{"curie": "MONDO:0002748", "names": ["rectal colloid adenocarcinoma", "Rectal Colloid Adenocarcinoma", "rectal mucinous adenocarcinoma", "Rectal Mucinous Adenocarcinoma", "rectum mucinous adenocarcinoma", "Rectal Colloidal Adenocarcinoma", "rectal colloidal adenocarcinoma", "colloid adenocarcinoma of rectum", "Colloid Adenocarcinoma of Rectum", "mucinous adenocarcinoma of rectum", "Mucinous Adenocarcinoma of Rectum", "colloidal adenocarcinoma of rectum", "Colloidal Adenocarcinoma of Rectum", "Colloidal adenocarcinoma of rectum", "colloid adenocarcinoma of the rectum", "Colloid Adenocarcinoma of the Rectum", "adenocarcinoma of the rectum, colloid", "mucinous adenocarcinoma of the rectum", "Mucinous Adenocarcinoma of the Rectum", "rectal, mucinous adenocarcinoma of the", "rectum, mucinous adenocarcinoma of the", "colloidal adenocarcinoma of the rectum", "adenocarcinoma of the rectum, mucinous", "Colloidal Adenocarcinoma of the Rectum", "mucinous adenocarcinoma of rectum (diagnosis)", "rectal neoplasm malignant adenocarcinoma mucinous"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rectum mucinous adenocarcinoma", "shortest_name_length": 29}
{"curie": "UMLS:C4528555", "names": ["Stage IIA Breast Cancer", "Anatomic Stage IIA Breast Cancer AJCC v8", "Anatomic Stage IIA Breast Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anatomic Stage IIA Breast Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "MONDO:0007846", "names": ["KBGS", "KBG syndrome", "KBG SYNDROME", "short stature-facial and skeletal anomalies-intellectual disability-macrodontia syndrome", "Short stature-facial and skeletal anomalies-intellectual disability-macrodontia syndrome", "Short stature, facial and skeletal anomalies, intellectual disability, macrodontia syndrome", "MACRODONTIA, MENTAL RETARDATION, CHARACTERISTIC FACIES, SHORT STATURE, AND SKELETAL ANOMALIES", "Short stature, characteristic facies, macrodontia, mental retardation, and skeletal anomalies", "macrodontia, mental retardation, characteristic facies, short stature, and skeletal anomalies", "short stature, characteristic facies, macrodontia, mental retardation, and skeletal anomalies", "Short stature-characteristic facies-mental retardation-macrodontia-skeletal anomalies syndrome", "short stature-characteristic facies-mental retardation-macrodontia-skeletal anomalies syndrome", "macrodontia, intellectual disability, characteristic facies, short stature, and skeletal anomalies", "short stature, characteristic facies, macrodontia, intellectual disability, and skeletal anomalies", "Short stature, facial and skeletal anomalies, intellectual disability, macrodontia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "KBG syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0004464", "names": ["urethra nephrogenic adenoma", "urethral nephrogenic adenoma", "Urethral Nephrogenic Adenoma", "nephrogenic adenoma of urethra", "Nephrogenic adenoma of urethra", "Nephrogenic Adenoma of Urethra", "Nephrogenic Adenoma of the Urethra", "nephrogenic adenoma of the urethra"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrogenic adenoma of the urethra", "shortest_name_length": 27}
{"curie": "UMLS:C0854824", "names": ["Stage III Anaplastic Large Cell Lymphoma", "Anaplastic Large Cell Lymphoma Stage III", "Ann Arbor Stage III Anaplastic Large Cell Lymphoma", "Anaplastic Large Cell Lymphoma T- and Null-Cell Types Stage III", "Anaplastic large cell lymphoma T- and null-cell types stage III", "Ann Arbor Stage III Noncutaneous Anaplastic Large Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Anaplastic Large Cell Lymphoma", "shortest_name_length": 40}
{"curie": "MONDO:0002910", "names": ["peroneal neuropathy", "Peroneal Neuropathy", "PERONEAL NEUROPATHY", "Neuropathy, Peroneal", "Fibular Nerve Disease", "Peroneal Neuropathies", "Fibular Nerve Diseases", "Peroneal Nerve Disease", "Nerve Disease, Fibular", "Peroneal Mononeuropathy", "Peroneal Nerve Diseases", "Mononeuropathy, Peroneal", "Peroneal nerve--Diseases", "Peroneal Mononeuropathies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroneal neuropathy", "shortest_name_length": 19}
{"curie": "MONDO:0013559", "names": ["HPS7", "HERMANSKY-PUDLAK SYNDROME 7", "Hermansky-Pudlak syndrome 7", "Hermansky-Pudlak syndrome type 7", "DTNBP1 Hermansky-Pudlak syndrome", "Hermansky-Pudlak syndrome caused by mutation in DTNBP1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hermansky-Pudlak syndrome 7", "shortest_name_length": 4}
{"curie": "UMLS:C3897539", "names": ["Stage II Anaplastic Large Cell Lymphoma", "Stage II Childhood Anaplastic Large Cell Lymphoma", "stage II childhood anaplastic large cell lymphoma", "Ann Arbor Stage II Childhood Anaplastic Large Cell Lymphoma", "Ann Arbor Stage II Noncutaneous Childhood Anaplastic Large Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Childhood Anaplastic Large Cell Lymphoma", "shortest_name_length": 39}
{"curie": "UMLS:C1869117", "names": ["mount-reback syndrome", "Mount-Reback syndrome", "mount reback syndrome", "Paroxysmal choreoathetosis", "paroxysmal choreoathetosis", "Paroxysmal choreo-athetosis", "Familial paroxysmal choreoathetosis", "Paroxysmal dystonic choreoathetosis", "Paroxysmal nonkinesigenic dyskinesia", "Paroxysmal nonkinesigenic dyskinesia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paroxysmal nonkinesigenic dyskinesia", "shortest_name_length": 21}
{"curie": "UMLS:C4745037", "names": ["Advanced Digestive System Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Digestive System Carcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C0234507", "names": ["Anosognosia", "anosognosia", "ANOSOGNOSIA", "Anosognosias", "anosognosias", "Anosognosia (finding)", "anosognosia (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anosognosia", "shortest_name_length": 11}
{"curie": "MONDO:0013651", "names": ["MRT18", "MED23", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 18", "mental retardation, autosomal recessive 18", "mental retardation, autosomal recessive type 18", "intellectual disability, autosomal recessive 18", "intellectual disability, autosomal recessive type 18", "autosomal recessive nonsyndromic mental retardation-18", "autosomal recessive intellectual developmental disorder 18", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 18", "autosomal recessive nonsyndromic intellectual disability-18", "MED23 autosomal recessive non-syndromic intellectual disability", "intellectual developmental disorder, autosomal recessive 18, with or without epilepsy", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 18, WITH OR WITHOUT EPILEPSY", "autosomal recessive non-syndromic intellectual disability caused by mutation in MED23"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 18", "shortest_name_length": 5}
{"curie": "MONDO:0033621", "names": ["SMAJI", "spinal muscular atrophy, infantile, James type", "SPINAL MUSCULAR ATROPHY, INFANTILE, JAMES TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal muscular atrophy, infantile, James type", "shortest_name_length": 5}
{"curie": "UMLS:C0729552", "names": ["Genital infection", "genital infection", "genital infections", "genitals infection", "Genital infection (disorder)", "Infectious disease of genitopelvic system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Genital infection", "shortest_name_length": 17}
{"curie": "UMLS:C1608942", "names": ["Complication of device insertion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Complication of device insertion", "shortest_name_length": 32}
{"curie": "UMLS:C0948715", "names": ["Infusion-Related Reaction", "Infusion Related Reaction", "Infusion related reaction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infusion-Related Reaction", "shortest_name_length": 25}
{"curie": "MONDO:0020645", "names": ["OPTA", "Marble Bone Disease", "Benign Osteopetrosis", "Albers-Schonberg Disease", "Albers-Schonberg disease", "Albers-Schönberg disease", "Albers-Schoenberg disease", "Autosomal Dominant Osteopetrosis", "autosomal dominant osteopetrosis", "osteopetrosis - autosomal dominant", "Autosomal Dominant Osteopetrosis Type 2", "autosomal dominant osteopetrosis (disease)", "osteopetrosis (disease), autosomal dominant", "osteopetrosis - autosomal dominant (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant osteopetrosis", "shortest_name_length": 4}
{"curie": "MONDO:0009013", "names": ["convulsive disorder, familial, with prenatal or early onset", "CONVULSIVE DISORDER, FAMILIAL, WITH PRENATAL OR EARLY ONSET", "Convulsive Disorder, Familial, with Prenatal or Early Onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "convulsive disorder, familial, with prenatal or early onset", "shortest_name_length": 59}
{"curie": "UMLS:C4684833", "names": ["Recurrent B Acute Lymphoblastic Leukemia", "Recurrent B-Cell Acute Lymphoblastic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent B Acute Lymphoblastic Leukemia", "shortest_name_length": 40}
{"curie": "MONDO:0000745", "names": ["SCA", "arrest", "arrested", "Asystole", "asystole", "ASYSTOLE", "Asystoles", "ASYSTOLIA", "asystolia", "Asystolic", "Asystolia", "HEART ARREST", "heart arrest", "Heart Arrest", "Heart arrest", "Arrest, Heart", "heart; arrest", "ARREST CARDIAC", "cardiac arrest", "CARDIAC ARREST", "Cardiac arrest", "Arrest cardiac", "Cardiac Arrest", "Arrest, Cardiac", "arrest; cardiac", "heart; stoppage", "stoppage; heart", "CARDIAC ASYSTOLE", "cardiac asystole", "Circulatory arrest", "STANDSTILL CARDIAC", "Ventricular arrest", "Standstill cardiac", "Cardiac standstill", "circulatory arrest", "arrest circulatory", "arrest; ventricular", "Asystole (disorder)", "circulatory; arrest", "Heart stops beating", "arrest; circulatory", "ventricular; arrest", "Arrest, circulatory", "CA - Cardiac arrest", "asystole (diagnosis)", "Ventricular asystole", "ventricular asystole", "VENTRICULAR ASYSTOLIA", "Ventricular asystolia", "cardiopulmonary arrest", "Cardiac arrest- asystole", "Cardiac arrest (disorder)", "Cardiac arrest - asystole", "cardiac arrest circulatory", "cardiac arrest (diagnosis)", "Cardiac arrest, unspecified", "arrest [as an cardiac arrest]", "Circulatory arrest (disorder)", "Circulatory arrest (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiac arrest", "shortest_name_length": 3}
{"curie": "MONDO:0007592", "names": ["Familial recurrent Bell palsy", "familial recurrent Bell palsy", "Familial recurrent peripheral facial palsy", "familial recurrent peripheral facial palsy", "Facial Palsy, Familial Recurrent Peripheral", "facial palsy, familial recurrent peripheral", "FACIAL PALSY, FAMILIAL RECURRENT PERIPHERAL", "Familial recurrent peripheral facial palsy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial recurrent peripheral facial palsy", "shortest_name_length": 29}
{"curie": "MONDO:0006095", "names": ["malignant carcinoid", "carcinoid malignant", "Carcinoid, malignant", "atypical carcinoid tumor", "Atypical Carcinoid Tumor", "Atypical carcinoid tumor", "malignant carcinoid tumor", "Malignant Carcinoid Tumor", "Atypical carcinoid tumour", "CARCINOID TUMOR MALIGNANT", "Malignant carcinoid tumor", "Malignant carcinoid tumour", "Carcinoid tumor, malignant", "Malignant carcinoid tumors", "atypical carcinoid tumor (diagnosis)", "Malignant carcinoid tumor (disorder)", "malignant carcinoid tumor (diagnosis)", "Atypical carcinoid tumor (morphologic abnormality)", "Malignant carcinoid tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical carcinoid tumor", "shortest_name_length": 19}
{"curie": "MONDO:0024686", "names": ["TGCT", "TSGCT", "diffuse-type GCT", "villous tenosynovitis", "Villous tenosynovitis", "Synovitis villonodular", "villonodular synovitis", "Villonodular synovitis", "Synovitis;villonodular", "Tenosynovitis, villous", "villonodular; synovitis", "synovitis; villonodular", "tenosynovial giant cell tumor", "diffuse-type giant cell tumor", "tenosynovial giant cell tumors", "pigmented villonodular synovitis", "Pigmented Villonodular Synovitis", "pigmented synovitis villonodular", "Pigmented villonodular synovitis", "Synovitis, Pigmented Villonodular", "Villonodular Synovitis, Pigmented", "Villonodular synovitis (pigmented)", "SYNOVITIS, VILLONODULAR, PIGMENTED", "Pigmented Villonodular Synovitides", "Villonodular Synovitides, Pigmented", "Synovitides, Pigmented Villonodular", "diffuse tenosynovial giant cell tumor", "Diffuse Tenosynovial Giant Cell Tumor", "Chronic hemorrhagic villous synovitis", "Tenosynovial giant cell tumor, diffuse", "Chronic haemorrhagic villous synovitis", "PVNS - Pigmented villonodular synovitis", "Tenosynovial giant cell tumour, diffuse", "diffuse giant cell tumor of Tenosynovium", "Diffuse Giant Cell Tumor of Tenosynovium", "Diffuse Tenosynovial Giant Cell Neoplasm", "diffuse pigmented villonodular synovitis", "Diffuse Giant cell tumor of Tenosynovium", "Villonodular synovitis, site unspecified", "diffuse tenosynovial giant cell neoplasm", "Diffuse Giant Cell Tumor of Tendon Sheath", "diffuse giant cell tumor of tendon sheath", "tenosynovial giant cell tumor diffuse type", "localized pigmented villonodular synovitis", "Pigmented villonodular synovitis (disorder)", "Diffuse Giant Cell Neoplasm of Tenosynovium", "Tenosynovial Giant Cell Tumor, Diffuse Type", "tenosynovial giant cell tumor, diffuse type", "diffuse giant cell neoplasm of Tenosynovium", "pigmented villonodular synovitis (diagnosis)", "diffuse giant cell neoplasm of tendon sheath", "Diffuse Giant Cell Neoplasm of Tendon Sheath", "Diffuse Giant Cell Tumor of the Tenosynovium", "diffuse giant cell tumor of the Tenosynovium", "Diffuse Giant Cell Neoplasm of the Tenosynovium", "diffuse giant cell neoplasm of the Tenosynovium", "Villonodular synovitis (pigmented), site unspecified", "Villonodular synovitis (pigmented), unspecified site", "Tenosynovial giant cell tumor, diffuse (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tenosynovial giant cell tumor, diffuse type", "shortest_name_length": 4}
{"curie": "UMLS:C4552685", "names": ["Stage I Vaginal Cancer", "Stage I Vaginal Cancer AJCC v8", "Stage I Vaginal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Vaginal Cancer AJCC v8", "shortest_name_length": 22}
{"curie": "MONDO:0009141", "names": ["DYT2", "torsion dystonia 2", "Torsion dystonia 2", "HPCA dystonic disorder", "torsion dystonia type 2", "Primary dystonia type 2", "Primary dystonia DYT2 type", "Primary dystonia, DYT2 type", "primary dystonia, DYT2 type", "DYSTONIA MUSCULORUM DEFORMANS 2", "dystonia musculorum deformans 2", "Dystonia Musculorum Deformans 2", "Primary dystonia type 2 (disorder)", "Dystonia musculorum deformans type 2", "dystonia musculorum deformans type 2", "autosomal recessive torsion dystonia 2", "Autosomal Recessive Torsion Dystonia 2", "Dystonia 2, Torsion, Autosomal Recessive", "dystonia 2, torsion, autosomal recessive", "DYSTONIA 2, TORSION, AUTOSOMAL RECESSIVE", "Dystonia, torsion, 2, autosomal recessive", "torsion dystonia 2, autosomal recessive type", "dystonic disorder caused by mutation in HPCA", "Torsion dystonia 2, autosomal recessive type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "torsion dystonia 2", "shortest_name_length": 4}
{"curie": "UMLS:C0687133", "names": ["Interactions", "drug interaction", "Drug interaction", "DRUG INTERACTION", "Drug Interaction", "Drug interactions", "Interaction, Drug", "Drug Interactions", "drug interactions", "Interactions, Drug", "Drug interaction NOS", "drug-drug interaction", "drug interaction with", "Drug drug interaction", "drug drug interaction", "INTERACTION DRUG (NOS)", "DRUG INTERACTION (NOS)", "Medication interaction", "Medication interactions", "Drug interaction with drug", "Drug interaction (finding)", "drug interaction (treatment)", "Drug interaction with drug (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drug Interactions", "shortest_name_length": 12}
{"curie": "MONDO:0013535", "names": ["glyoxalase 2 deficiency", "Glyoxalase II Deficiency", "glyoxalase II deficiency", "GLYOXALASE II DEFICIENCY", "hydroxyacyl glutathione hydrolase deficiency", "HYDROXYACYL GLUTATHIONE HYDROLASE DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hydroxyacyl glutathione hydrolase deficiency", "shortest_name_length": 23}
{"curie": "UMLS:C5206590", "names": ["Epididymal Cystadenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epididymal Cystadenoma", "shortest_name_length": 22}
{"curie": "MONDO:0060707", "names": ["VERBRAS", "Ververi Brady syndrome", "VERVERI-BRADY SYNDROME", "Ververi-Brady syndrome", "QRICH1-related intellectual disability-chondrodysplasia syndrome", "QRICH1-related intellectual disability, chondrodysplasia syndrome", "Glutamine rich 1-related intellectual disability, chondrodysplasia syndrome", "Glutamine rich 1-related intellectual disability, chondrodysplasia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ververi-Brady syndrome", "shortest_name_length": 7}
{"curie": "UMLS:C0281242", "names": ["AIDS Related Diffuse Large Cell Lymphoma", "AIDS-Related Diffuse Large Cell Lymphoma", "AIDS-related diffuse large cell lymphoma", "diffuse large cell lymphoma, AIDS-related", "AIDS-Associated Diffuse Large Cell Lymphoma", "AIDS Associated Diffuse Large Cell Lymphoma", "AIDS-associated diffuse large cell lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Diffuse Large Cell Lymphoma", "shortest_name_length": 40}
{"curie": "MONDO:0006392", "names": ["rectal MP", "rectal Hp", "Rectal HP", "Rectal MP", "Rectal Metaplastic Polyp", "rectal metaplastic polyp", "Rectal hyperplastic polyp", "Rectal Hyperplastic Polyp", "rectal hyperplastic polyp", "hyperplastic polyp of rectum", "Hyperplastic Polyp of Rectum", "Hyperplastic Polyp of the Rectum", "hyperplastic polyp of the rectum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rectal hyperplastic polyp", "shortest_name_length": 9}
{"curie": "MONDO:0004779", "names": ["epididymis", "EPIDIDYMIS", "epididymal", "Epididymal", "Epididymis", "epididymitis", "Epididymitis", "EPIDIDYMITIS", "Epididymitides", "Epididymitis NOS", "Epididymitis, NOS", "Epididymis inflamed", "epididymitis (disease)", "Epididymitis (disorder)", "epididymitis (diagnosis)", "epididymis; inflammation", "inflammation; epididymis", "Inflammation of epididymis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epididymitis", "shortest_name_length": 10}
{"curie": "MONDO:0001146", "names": ["Palsy;IV nerve", "iv nerve palsy", "IV nerve palsy", "nerve iv palsy", "4th nerve palsy", "IV thnerve palsy", "ivth nerve palsy", "IVth nerve palsy", "fourth nerve palsy", "Fourth nerve palsy", "Fourth Nerve Palsy", "IVth nerve paresis", "Palsy, Fourth Nerve", "Fourth nerve paresis", "Fourth Nerve Palsies", "IVth nerve paralysis", "Trochlear Nerve Palsy", "trochlear nerve palsy", "Palsies, Fourth Nerve", "Trochlear nerve palsy", "superior oblique palsy", "Cranial Nerve IV Palsy", "Superior oblique palsy", "Cranial nerve palsy IV", "Fourth nerve paralysis", "Palsy, Trochlear Nerve", "nerve palsies trochlear", "Trochlear Nerve Palsies", "n.trochlearis; paralysis", "Trochlear nerve weakness", "Palsies, Trochlear Nerve", "Trochlear nerve paralysis", "paralysis; trochlear nerve", "fourth cranial nerve palsy", "Fourth Cranial Nerve Palsy", "fourth nerve cranial palsy", "Fourth cranial nerve palsy", "Disorder of trochlear nerve", "Disorder of cranial nerve 4", "Fourth cranial nerve paresis", "Fourth nerve palsy (disorder)", "Fourth cranial nerve paralysis", "Fourth [trochlear] nerve palsy", "fourth nerve palsy (diagnosis)", "fourth or trochlear nerve palsy", "Fourth or trochlear nerve palsy", "Paresis of fourth cranial nerve", "CRANIAL NERVE PALSY IV TROCHLEAR", "paralysis; cranial nerve, fourth", "trochlear nerve cranial nerve palsy", "cranial nerve palsy of trochlear nerve"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fourth cranial nerve palsy", "shortest_name_length": 14}
{"curie": "MONDO:0015452", "names": ["CSS", "HHID", "fifth digit syndrome", "FIFTH DIGIT SYNDROME", "Fifth Digit Syndrome", "Fifth digit syndrome", "Coffin-Siris syndrome", "coffin-siris syndrome", "Coffin Siris syndrome", "COFFIN-SIRIS SYNDROME", "Coffin-Siris Syndrome", "coffin siris syndrome", "dwarfism-onychodysplasia", "Dwarfism-Onychodysplasia", "Short Stature-Onychodysplasia.", "short stature-onychodysplasia.", "Coffin-Siris syndrome (disorder)", "dwarfism-onychodysplasia syndrome", "Coffin-Siris syndrome (diagnosis)", "intellectual disability with absent fifth fingernail and terminal phalanx", "HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVE FACIAL FEATURES", "Hypertrichosis, hyperkeratosis, mental retardation, and distinctive facial features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Coffin-Siris syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C0560632", "names": ["lumbar; injury", "injury; lumbar", "lower back injury", "Lower back injury", "Lower Back Injury", "back injuries lower", "Lumbar region injury", "BACK INJURY LOWER BACK", "Lower back injury (disorder)", "lower back injury (diagnosis)", "back disorders injuries lower"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lower back injury", "shortest_name_length": 14}
{"curie": "UMLS:C5420327", "names": ["Salivary Gland Lymphadenoma", "Lymphadenoma, Salivary Gland", "Salivary Gland Lymphadenomas", "Lymphadenomas, Salivary Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Salivary Gland Lymphadenomas", "shortest_name_length": 27}
{"curie": "MONDO:0002303", "names": ["CRVO", "retinal central vein occlusion", "Central retinal vein occlusion", "Central Retinal Vein Occlusion", "central retinal vein occlusion", "Central retinal vein thrombosis", "central occlusions retinal vein", "central retinal thrombosis vein", "Central Retinal Venous Occlusion", "central retinal Venous occlusion", "occlusion of central retinal vein", "CRVO - Central retinal vein occlusion", "CRVT - Central retinal vein thrombosis", "Central retinal vein occlusion (disorder)", "central retinal vein occlusion (diagnosis)", "central retinal vein retinal vein occlusion", "retinal vein occlusion of central retinal vein", "occlusion of central retinal vein (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central retinal vein occlusion", "shortest_name_length": 4}
{"curie": "MONDO:0008157", "names": ["Bos", "BOS", "Curth's syndrome", "Dermatoosteopoikilosis", "DERMATOOSTEOPOIKILOSIS", "dermatoosteopoikilosis", "Dermato-osteopoikilosis", "Isolated osteopoikilosis", "OSTEOPOIKILOSIS, ISOLATED", "Osteopoikilosis, Isolated", "osteopoikilosis, isolated", "buschke-ollendorf syndrome", "Buschke-Ollendorf syndrome", "BUSCHKE-OLLENDORFF SYNDROME", "Buschke-Ollendorff syndrome", "buschke-ollendorff syndrome", "Buschke Ollendorff syndrome", "Disseminated dermatofibrosis", "Dermato-osteopoikilosis syndrome", "OSTEOPATHIA CONDENSANS DISSEMINATA", "osteopathia condensans disseminata", "Osteopathia condensans disseminata", "Isolated osteopoikilosis (disorder)", "osteopoikilosis with melorheostosis", "Dermatofibrosis lenticularis disseminata", "osteopoikilosis with or without melorheostosis", "disseminated dermatofibrosis with osteopoikilosis", "Disseminated dermatofibrosis with osteopoikilosis", "DERMATOFIBROSIS LENTICULARIS DISSEMINATA, ISOLATED", "dermatofibrosis, disseminated with osteopoikilosis", "dermatofibrosis lenticularis disseminata, isolated", "Dermatofibrosis, disseminated, with osteopoikilosis", "dermatofibrosis, disseminated, with osteopoikilosis", "DERMATOFIBROSIS, DISSEMINATED, WITH OSTEOPOIKILOSIS", "Dermatofibrosis lenticularis disseminata (disorder)", "dermatofibrosis lenticularis disseminata with osteopoikilosis", "Dermatofibrosis lenticularis disseminata with osteopoikilosis", "DERMATOFIBROSIS LENTICULARIS DISSEMINATA WITH OSTEOPOIKILOSIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Buschke-Ollendorff syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0005580", "names": ["ESCC", "Esophagus SCC", "esophagus scc", "esophageal scc", "Esophageal SCC", "SCC of Esophagus", "SCC of esophagus", "scc of esophagus", "SCC of oesophagus", "SCC of the Esophagus", "scc of the esophagus", "squamous cell car. - esophagus", "squamous cell esophagus cancer", "Squamous cell car. - esophagus", "ESOPHAGEAL CANCER SQUAMOUS CELL", "Esophageal Squamous Cell Cancer", "esophageal squamous cell cancer", "Esophageal Epidermoid Carcinoma", "squamous cell esophageal cancer", "esophageal epidermoid carcinoma", "Esophageal epidermoid carcinoma", "esophagus cancer, squamous cell", "esophageal cancer, squamous cell", "esophagus squamous cell carcinoma", "carcinoma cell esophagus squamous", "Esophagus Squamous Cell Carcinoma", "Esophageal squamous cell carcinoma", "oesophagus squamous cell carcinoma", "esophageal squamous cell carcinoma", "Esophageal Squamous Cell Carcinoma", "Oesophageal squamous cell carcinoma", "Oesophageal Squamous Cell Carcinoma", "Esophageal epidermoid carcinoma NOS", "Squamous cell carcinoma of esophagus", "Squamous Cell Carcinoma of Esophagus", "squamous cell carcinoma of esophagus", "Oesophageal epidermoid carcinoma NOS", "Squamous cell carcinoma of oesophagus", "Esophageal squamous cell carcinoma NOS", "Oesophageal squamous cell carcinoma NOS", "Esophageal Squamous Cell Carcinoma, NOS", "Squamous cell carcinoma of esophagus NOS", "Squamous cell carcinoma of the esophagus", "Squamous Cell Carcinoma of the Esophagus", "squamous cell carcinoma of the esophagus", "SCC - Squamous cell carcinoma of esophagus", "SCC - Squamous cell carcinoma of oesophagus", "[OBSOLETE] Esophageal Squamous Cell Carcinoma", "Squamous cell carcinoma of esophagus (disorder)", "squamous cell carcinoma of esophagus (diagnosis)", "Esophageal squamous cell carcinoma stage unspecified", "Oesophageal squamous cell carcinoma stage unspecified", "Esophageal Squamous Cell Carcinoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophageal squamous cell carcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0012585", "names": ["CHDS7", "CD36 coronary artery disease", "susceptibility to coronary heart disease 7", "CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 7", "coronary heart disease, susceptibility to, 7", "coronary heart disease, susceptibility to, type 7", "coronary artery disease caused by mutation in CD36"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coronary heart disease, susceptibility to, 7", "shortest_name_length": 5}
{"curie": "MONDO:0022756", "names": ["monosomy 1q", "deletion 1q", "1q monosomy", "1q deletion", "partial monosomy 1q", "chromosome 1q deletion", "partial deletion of chromosome 1q", "partial monosomy of chromosome 1q", "partial deletion of the long arm of chromosome 1", "partial monosomy of the long arm of chromosome 1", "partial deletion of the long arm of chromosome type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 1q deletion", "shortest_name_length": 11}
{"curie": "UMLS:C3640140", "names": ["Stage I Differentiated Thyroid Gland Cancer Under 45 Years", "Stage I Differentiated Thyroid Gland Carcinoma Under 45 Years", "Stage I Differentiated Thyroid Gland Carcinoma Under 45 Years AJCC v7", "Stage I Thyroid Gland Papillary or Follicular Carcinoma Under 45 Years"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Differentiated Thyroid Gland Carcinoma Under 45 Years AJCC v7", "shortest_name_length": 58}
{"curie": "UMLS:C1112306", "names": ["Adenoviral hepatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenoviral hepatitis", "shortest_name_length": 20}
{"curie": "MONDO:0009422", "names": ["Sweat Gland Hypoplasia", "sweat gland hypoplasia", "SWEAT GLAND HYPOPLASIA", "HYPOHIDROSIS WITH ABNORMAL PALMAR DERMAL RIDGES", "hypohidrosis with abnormal palmar dermal Ridges", "Hypohidrosis with Abnormal Palmar Dermal Ridges"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypohidrosis with abnormal palmar dermal Ridges", "shortest_name_length": 22}
{"curie": "MONDO:0001083", "names": ["RFS", "FRTS", "Fanconi", "Fanconi syndrome", "FANCONI SYNDROME", "fanconi syndrome", "Fanconi Syndrome", "fanconis syndrome", "Syndrome, Fanconi", "Fanconi's syndrome", "adult Fanconi Anemia", "Fanconi syndrome, NOS", "RENAL FANCONI SYNDROME", "Renal Fanconi syndrome", "Adult Fanconi syndrome", "ADULT FANCONI SYNDROME", "adult Fanconi syndrome", "Renal Fanconi Syndrome", "LUDER-SHELDON SYNDROME", "Adult Fanconi Syndrome", "Luder-Sheldon Syndrome", "Luder-Sheldon syndrome", "Luder Sheldon Syndrome", "nephropathic cystinosis", "Fanconi Syndrome, Renal", "Lignac-Fanconi Syndrome", "deToni Fanconi syndrome", "Syndrome, Adult Fanconi", "Nephropathic cystinosis", "Lignac-Fanconi syndrome", "Syndrome, Luder-Sheldon", "Syndrome, Renal Fanconi", "Fanconi Syndrome, Adult", "Fanconi-de Toni syndrome", "Fanconi-de-Toni syndrome", "Adult Fanconi's Syndrome", "Primary Fanconi Syndrome", "De toni-Fanconi syndrome", "Fanconi-de toni syndrome", "Fanconi-de-toni syndrome", "Primary Fanconi syndrome", "De Toni-Fanconi syndrome", "Fanconi syndrome (disorder)", "Fanconi syndrome congenital", "Toni-Debre-Fanconi Syndrome", "congenital Fanconi syndrome", "toni-debre-Fanconi syndrome", "Congenital Fanconi syndrome", "Glucoaminophosphate diabetes", "FANCONI RENOTUBULAR SYNDROME", "Fanconi renotubular syndrome", "Fanconi syndrome (diagnosis)", "Fanconi Renotubular Syndrome", "Renotubular Syndrome, Fanconi", "Syndrome, Fanconi Renotubular", "Renal tubular fanconi syndrome", "Renal tubular Fanconi syndrome", "De toni-fanconi-debre syndrome", "de Toni-Debre-Fanconi syndrome", "Fanconi-de Toni-Debre syndrome", "De toni-debre-Fanconi syndrome", "De Toni-Debre-Fanconi Syndrome", "Glucoaminophosphaturia syndrome", "Infantile nephropathic cystinosis", "Adult Fanconi syndrome (disorder)", "infantile nephropathic cystinosis", "Proximal renal tubular dysfunction", "Proximal Renal Tubular Dysfunction", "Primary Toni-Debre-Fanconi Syndrome", "Fanconi Syndrome without Cystinosis", "FANCONI SYNDROME WITHOUT CYSTINOSIS", "Congenital Fanconi syndrome (disorder)", "Congenital Fanconi syndrome (diagnosis)", "Neonatal De Toni-Debre-Fanconi Syndrome", "Idiopathic De Toni-Debre-Fanconi Syndrome", "Amino acid-glucose defective tubular absorption", "Hepatic glycogenosis with de Toni-Debré-Fanconi syndrome", "Hepatic glycogenosis with de Toni-Debre-Fanconi syndrome", "cystinosis infantile nephropathic congenital Fanconi syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fanconi renotubular syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0001761", "names": ["FAVISM", "favism", "Favism", "Favisms", "favism; anemia", "anemia; favism", "favism; poisoning", "Favism (disorder)", "poisoning; favism", "favism (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "favism", "shortest_name_length": 6}
{"curie": "MONDO:0016099", "names": ["overlap myositis", "non-specific myositis", "adult-onset overlap myositis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "overlap myositis", "shortest_name_length": 16}
{"curie": "MONDO:0013825", "names": ["DIAR6", "diarrhea 6", "DIARRHEA 6", "diarrhea type 6", "congenital diarrhea 6", "congenital diarrhoea 6", "congenital diarrhea type 6", "GUCY2C congenital diarrhea", "congenital diarrhea caused by mutation in GUCY2C", "chronic diarrhea due to guanylate cyclase 2C overactivity", "chronic diarrhoea due to guanylate cyclase 2C overactivity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital diarrhea 6", "shortest_name_length": 5}
{"curie": "MONDO:0013748", "names": ["VSD2", "VENTRICULAR SEPTAL DEFECT 2", "ventricular septal defect 2", "ventricular septal defect type 2", "ventricular septal defect - VSD2", "CITED2 ventricular septal defect (disease)", "ventricular septal defect - VSD2 (diagnosis)", "ventricular septal defect (disease) caused by mutation in CITED2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ventricular septal defect 2", "shortest_name_length": 4}
{"curie": "UMLS:C3544335", "names": ["Contrast encephalopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Contrast encephalopathy", "shortest_name_length": 23}
{"curie": "MONDO:0002177", "names": ["insulin high", "Insulin high", "high insulin", "hyperinsulism", "Hyperinsulinism", "hyperinsulinism", "Hyperinsulinemia", "HYPERINSULINEMIA", "INSULIN INCREASE", "hyperinsulinemia", "Insulin increased", "hyperinsulinaemia", "Hyperinsulinaemia", "increased insulin", "Increased insulin", "increasing insulin", "Hyperinsulinism NOS", "Hyperinsulinism, NOS", "Elevated insulin level", "Elevated insulin levels", "Hyperinsulinism syndrome", "hyperinsulinism (disease)", "Hyperinsulinism (disorder)", "hyperinsulinism (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperinsulinism", "shortest_name_length": 12}
{"curie": "MONDO:0016208", "names": ["Solitary ulcer syndrome", "Solitary rectal ulcer syndrome", "solitary rectal ulcer syndrome", "Solitary rectal ulcer syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "solitary rectal ulcer syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0018573", "names": ["intrauterine growth restriction-short stature-early adult-onset diabetes syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intrauterine growth restriction-short stature-early adult-onset diabetes syndrome", "shortest_name_length": 81}
{"curie": "UMLS:C5237322", "names": ["Proximal Gastric Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Proximal Gastric Adenocarcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C1334855", "names": ["Myxoid Chondrosarcoma NCI Grade 2", "Myxoid Chondrosarcoma NCI Grade II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myxoid Chondrosarcoma NCI Grade 2", "shortest_name_length": 33}
{"curie": "MONDO:0006680", "names": ["Blue Nevi", "Blue nevi", "blue nevus", "Nevi, Blue", "Blue nevus", "nevus blue", "Blue Nevus", "BLUE NEVUS", "blue naevus", "Nevus, Blue", "Naevus;blue", "Blue naevus", "Blue nevus NOS", "Blue naevus NOS", "blue skin Nevus", "Blue Skin Nevus", "Blue nevus, NOS", "blue neuronevus", "Blue naevus, NOS", "Blue nevus of skin", "blue Nevus of skin", "Blue Nevus of Skin", "Dermal melanocytoma", "Blue naevus of skin", "Jadassohn; blue nevus", "blue nevus; Jadassohn", "Jadassohn-Tièche nevus", "Tièche-Jadassohn nevus", "blue Nevus of the skin", "Jadassohn's blue nevus", "Blue Nevus of the Skin", "Jadassohn's blue naevus", "Jadassohn-TiC(che nevus", "Jadassohn-Tièche syndrome", "benign blue nevus of skin", "Jadassohn-TiC(che syndrome", "benign blue nevus neoplasm", "benign mesenchymal melanoma", "Blue nevus of skin (disorder)", "Blue nevus (morphologic abnormality)", "benign blue nevus of skin (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blue nevus", "shortest_name_length": 9}
{"curie": "MONDO:0015100", "names": ["Aregenerative anemia", "aregenerative anemia", "Aregenerative anaemia", "ANEMIA, AREGENERATIVE", "Nonregenerative anemia", "Non regenerative anemia", "Non regenerative anaemia", "Anemia aplastic aregenerative", "ANEMIA APLASTIC AREGENERATIVE", "Anaemia aplastic aregenerative", "nonregenerative aplastic anemia", "Nonregenerative anemia (disorder)", "nonregenerative aplastic anemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aregenerative anemia", "shortest_name_length": 20}
{"curie": "MONDO:0030939", "names": ["POF18", "premature ovarian failure 18", "PREMATURE OVARIAN FAILURE 18", "primary ovarian insufficiency 18"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "premature ovarian failure 18", "shortest_name_length": 5}
{"curie": "MONDO:0022791", "names": ["Sondheimer syndrome", "coarse face hypotonia constipation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coarse face hypotonia constipation", "shortest_name_length": 19}
{"curie": "MONDO:0011102", "names": ["DFNA8", "DFNA12", "autosomal dominant deafness 8", "deafness, autosomal dominant 8", "Deafness, Autosomal Dominant 8", "autosomal dominant deafness 12", "DEAFNESS, AUTOSOMAL DOMINANT 8", "DEAFNESS, AUTOSOMAL DOMINANT 12", "deafness, autosomal dominant 12", "Deafness, Autosomal Dominant 12", "deafness, autosomal dominant 8/12", "deafness, autosomal dominant type 12", "autosomal dominant nonsyndromic deafness 12", "TECTA autosomal dominant nonsyndromic deafness", "autosomal dominant nonsyndromic hearing loss 12", "autosomal dominant nonsyndromic deafness type 12", "autosomal dominant nonsyndromic deafness caused by mutation in TECTA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 12", "shortest_name_length": 5}
{"curie": "MONDO:0002682", "names": ["brain ventricle cancer", "Brain Ventricular Tumor", "Brain Ventricular Tumors", "Tumor, Brain Ventricular", "Ventricular Tumor, Brain", "Cerebral Ventricle Tumor", "cerebral ventricle cancer", "Ventricular Tumors, Brain", "cancer of brain ventricle", "Cerebral Ventricle Tumors", "Tumors, Brain Ventricular", "Tumor, Cerebral Ventricle", "Ventricle Tumor, Cerebral", "Intraventricular Neoplasm", "intraventricular neoplasms", "Brain Ventricular Neoplasm", "Intraventricular Neoplasms", "Neoplasm, Intraventricular", "Ventricle Tumors, Cerebral", "Tumors, Cerebral Ventricle", "Brain Ventricular Neoplasms", "Cerebroventricular Neoplasm", "cerebral ventricle neoplasm", "Ventricular Neoplasm, Brain", "Neoplasms, Intraventricular", "Neoplasm, Brain Ventricular", "Cerebral Ventricle Neoplasm", "Intraventricular Brain Tumor", "Ventricular Neoplasms, Brain", "Cerebroventricular Neoplasms", "Cerebral Ventricle Neoplasms", "Neoplasm, Cerebral Ventricle", "Neoplasm, Cerebroventricular", "Neoplasms, Brain Ventricular", "intraventricular brain tumor", "Neoplasms, Cerebral Ventricle", "Neoplasms, Ventricular, Brain", "Neoplasms, Cerebroventricular", "Neoplasm of cerebral ventricle", "neoplasm of cerebral ventricle", "intraventricular brain neoplasm", "Intraventricular Brain Neoplasm", "intraventricular tumor of brain", "Intraventricular Tumor of Brain", "Intraventricular tumor of brain", "Intraventricular Brain Neoplasms", "Malignant neoplasm of ventricles", "intraventricular brain neoplasms", "Brain Neoplasms, Intraventricular", "brain neoplasms, intraventricular", "Intraventricular Neoplasm of Brain", "intraventricular neoplasm of brain", "malignant brain ventricle neoplasm", "intraventricular tumor of the brain", "Intraventricular Tumor of the Brain", "malignant neoplasm of brain ventricle", "malignant tumor of cerebral ventricle", "Intraventricular Neoplasm of the Brain", "intraventricular neoplasm of the brain", "Malignant neoplasm of cerebral ventricle", "malignant neoplasm of cerebral ventricle", "Malignant neoplasm of cerebral ventricles", "Neoplasm of cerebral ventricle (disorder)", "neoplasm of cerebral ventricle (diagnosis)", "malignant neoplasm of cerebral ventricle (diagnosis)", "Malignant neoplasm of cerebral ventricles (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral ventricle cancer", "shortest_name_length": 22}
{"curie": "MONDO:0005739", "names": ["Echinostomosis", "echinostomiasis", "Echinostomiasis", "Echinochasmosis", "Echinostomiases", "ECHINOSTOMIASIS", "Echinostomatidosis", "infection by Echinochasmus", "Infection by Echinochasmus", "Echinostomiasis (disorder)", "infection due to Echinochasmus", "Infection by Echinochasmus, NOS", "Infection caused by Echinochasmus", "Echinostomatoidea infectious disease", "Echinostomatoidea disease or disorder", "infection due to Echinochasmus (diagnosis)", "Echinostomatoidea caused disease or disorder", "Infection caused by Echinochasmus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "echinostomiasis", "shortest_name_length": 14}
{"curie": "MONDO:0017972", "names": ["classic CLAH", "classic congenital lipoid adrenal hyperplasia due to STAR deficency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "classic congenital lipoid adrenal hyperplasia due to STAR deficency", "shortest_name_length": 12}
{"curie": "UMLS:C0856705", "names": ["Encephalomyelitis infection", "infectious encephalomyelitis", "Infectious Encephalomyelitis", "Infectious encephalomyelitis", "Infection causing encephalomyelitis", "Infection causing encephalomyelitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infectious Encephalomyelitis", "shortest_name_length": 27}
{"curie": "MONDO:0006234", "names": ["pin III", "PIN III", "Grade 3 PIN", "grade 3 pin", "Grade III PIN", "grade III PIN", "grade III pin", "Cancer in situ of prostate", "prostate carcinoma in situ", "carcinoma in situ of prostate", "Carcinoma in situ of prostate", "Prostate Adenocarcinoma in situ", "prostate adenocarcinoma in situ", "stage 0 prostate gland carcinoma", "prostate gland carcinoma in situ", "prostate gland in situ carcinoma", "Adenocarcinoma in situ of Prostate", "adenocarcinoma in situ of prostate", "carcinoma in situ of prostate gland", "CIS - Carcinoma in situ of prostate", "Adenocarcinoma in situ of the Prostate", "adenocarcinoma in situ of the prostate", "Carcinoma in situ of prostate (disorder)", "Grade 3 Prostatic Intraepithelial Neoplasia", "grade 3 prostatic intraepithelial neoplasia", "grade III prostatic intraepithelial neoplasia", "Grade III Prostatic Intraepithelial Neoplasia", "Prostatic intraepithelial neoplasia grade III", "Prostatic intraepithelial neoplasia, grade III", "High grade prostatic intraepithelial neoplasia", "carcinoma in situ of prostate gland (diagnosis)", "PIN III - prostatic intraepithelial neoplasia grade III", "High grade prostatic intraepithelial neoplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "grade III prostatic intraepithelial neoplasia", "shortest_name_length": 7}
{"curie": "MONDO:0002293", "names": ["skin ganglioneuroma", "Skin Ganglioneuroma", "Ganglioneuroma of skin", "ganglioneuroma of skin", "Ganglioneuroma of Skin", "Cutaneous Ganglioneuroma", "cutaneous ganglioneuroma", "ganglioneuroma of the skin", "Ganglioneuroma of the Skin", "Ganglioneuroma of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous ganglioneuroma", "shortest_name_length": 19}
{"curie": "UMLS:C1333119", "names": ["Colorectal Villous Adenoma", "Large Bowel Villous Adenoma", "Villous Adenoma of Large Bowel", "Villous Adenoma of the Large Bowel"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Villous Adenoma", "shortest_name_length": 26}
{"curie": "MONDO:0006965", "names": ["Clubbing", "Acropachy", "acropachy", "club finger", "club fingers", "clubbed finger", "Clubbed Finger", "clubbed fingers", "Finger Clubbing", "Clubbed fingers", "finger clubbing", "Bamberger-Marie", "clubbing finger", "Finger clubbing", "FINGER CLUBBING", "Clubbed Fingers", "Finger, Clubbed", "Marie-Bamberger", "digital clubbing", "Fingers, Clubbed", "clubbing fingers", "fingers clubbing", "Clubbing (hands)", "Finger(s) Clubbed", "Drumstick fingers", "drumstick fingers", "Drumstick Fingers", "Clubbing of Fingers", "clubbing of fingers", "Hippocratic Fingers", "Clubbing of fingers", "FC - Finger clubbing", "Clubbing (of fingers)", "clubbing of finger(s)", "Clubbing of the fingers", "bamberger-marie disease", "Marie Bamberger Disease", "Marie-Bamberger Disease", "Bamberger-Marie disease", "Marie-Bamberger disease", "Marie Bamberger disease", "Disease, Marie-Bamberger", "Finger clubbing (disorder)", "OSTEOARTHROPATHY HYPERTROPHIC", "HYPERTROPHIC OSTEOARTHROPATHY", "Hypertrophic osteoarthropathy", "hypertrophic osteoarthropathy", "OSTEOARTHROPATHY, HYPERTROPHIC", "hypertrophic; osteoarthropathy", "osteoarthropathy; hypertrophic", "Pachydermoperiostitis acquired", "HOA - Hypertrophic osteoarthropathy", "secondary hypertrophic osteoarthropathy", "Pulmonary osteoarthropathy hypertrophic", "Secondary hypertrophic osteoarthropathy", "Hypertrophic Pulmonary Osteoarthropathy", "hypertrophic pulmonary osteoarthropathy", "Hypertrophic pulmonary osteoarthropathy", "Secondary Hypertrophic Osteoarthropathy", "Hypertrophic Osteoarthropathy, Secondary", "osteoarthropathy; secondary hypertrophic", "secondary; hypertrophic osteoarthropathy", "Hypertrophic osteoarthropathy (disorder)", "Osteoarthropathy, Secondary Hypertrophic", "Secondary Hypertrophic Osteoarthropathies", "secondary; osteoarthropathy, hypertrophic", "Osteoarthropathy, hypertrophic, secondary", "hypertrophic; osteoarthropathy, pulmonary", "hypertrophic osteoarthropathy (diagnosis)", "osteoarthropathy; hypertrophic, pulmonary", "Hypertrophic Osteoarthropathies, Secondary", "Osteoarthropathies, Secondary Hypertrophic", "HPOA - hypertrophic pulmonary osteoarthropathy", "HPOA - Hypertrophic pulmonary osteoarthropathy", "hypertrophic pulmonary osteoarthropathy (diagnosis)", "hypertrophic pulmonary osteoarthropathy (disorder) [ambiguous]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary hypertrophic osteoarthropathy", "shortest_name_length": 8}
{"curie": "MONDO:0002529", "names": ["CSCC", "Spinous cell carcinoma", "Squamous skin carcinoma", "Skin Squamous Cell Cancer", "squamous cell skin cancer", "SKIN CANCER SQUAMOUS CELL", "cancer cell skin squamous", "Epidermoid Skin Carcinoma", "epidermoid skin carcinoma", "Epidermoid skin carcinoma", "skin squamous cell cancer", "cancers cell skin squamous", "skin cancer, squamous cell", "carcinoma, epidermoid, skin", "Squamous Cell Skin Carcinoma", "skin squamous cell carcinoma", "Skin Squamous Cell Carcinoma", "epidermoid carcinoma of skin", "squamous cell skin carcinoma", "squamous cell carcinoma skin", "carcinoma cell skin squamous", "Epidermoid Carcinoma of Skin", "carcinoma, squamous cell, skin", "squamous cell carcinoma - skin", "Squamous cell carcinoma - skin", "squamous cell carcinoma of skin", "Squamous cell carcinoma of skin", "Squamous Cell Carcinoma of Skin", "SQUAMOUS CELL CARCINOMA OF SKIN", "epidermoid carcinoma of the skin", "Epidermoid Carcinoma of the Skin", "cancer of the skin, squamous cell", "Cutaneous squamous cell carcinoma", "Cutaneous Squamous Cell Carcinoma", "skin cancer, epidermoid carcinoma", "cutaneous squamous cell carcinoma", "squamous cell carcinoma of the skin", "Squamous Cell Carcinoma of the Skin", "Squamous cell carcinoma of the skin", "zone of skin squamous cell carcinoma", "carcinoma of the skin, squamous cell", "SCC - Squamous cell carcinoma of skin", "SCC - Cutaneous squamous cell carcinoma", "Squamous cell carcinoma of skin (disorder)", "squamous cell carcinoma of skin (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin squamous cell carcinoma", "shortest_name_length": 4}
{"curie": "UMLS:C4763799", "names": ["Recurrent Subcutaneous Panniculitis-Like T-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Subcutaneous Panniculitis-Like T-Cell Lymphoma", "shortest_name_length": 56}
{"curie": "MONDO:0018640", "names": ["secondary vasculitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary vasculitis", "shortest_name_length": 20}
{"curie": "UMLS:C5421213", "names": ["Metastatic Malignant Neoplasm in the Visual Pathway"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Malignant Neoplasm in the Visual Pathway", "shortest_name_length": 51}
{"curie": "UMLS:C0751395", "names": ["Mixed Oligodendroglioma-Ependymoma", "Mixed Oligodendroglioma Ependymoma", "Oligodendroglioma-Ependymoma, Mixed", "Mixed Oligodendroglioma-Ependymomas", "Oligodendroglioma-Ependymomas, Mixed"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mixed Oligodendroglioma-Ependymoma", "shortest_name_length": 34}
{"curie": "UMLS:C5419189", "names": ["Metastatic Chromophobe Renal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Chromophobe Renal Cell Carcinoma", "shortest_name_length": 43}
{"curie": "UMLS:C2931753", "names": ["X-linked achromatopsia, incomplete", "Achromatopsia incomplete, X-linked", "Incomplete achromatopsia , X-linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Achromatopsia incomplete, X-linked", "shortest_name_length": 34}
{"curie": "UMLS:C1334027", "names": ["High Risk Small Intestinal GIST", "High Risk Small Intestinal Gastrointestinal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Risk Small Intestinal Gastrointestinal Stromal Tumor", "shortest_name_length": 31}
{"curie": "UMLS:C4288036", "names": ["Vaginal Papillary Carcinoma", "Vaginal Squamotransitional Carcinoma", "Vaginal Squamotransitional Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Papillary Carcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C0152874", "names": ["ear; tuberculous", "Ear tuberculosis", "tuberculosis; ear", "tuberculosis of ear", "Tuberculosis of ear", "Tuberculosis of the ear, NOS", "Tuberculosis of ear (disorder)", "tuberculosis of ear (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tuberculosis of ear", "shortest_name_length": 16}
{"curie": "UMLS:C2930471", "names": ["Bilateral Wilms Tumor", "Wilms Tumor, Bilateral", "Tumor, Bilateral Wilms", "Wilms tumor, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bilateral Wilms Tumor", "shortest_name_length": 21}
{"curie": "UMLS:C3502214", "names": ["Microcephalic Osteodysplastic Primordial Dwarfism with Tooth Abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Microcephalic Osteodysplastic Primordial Dwarfism with Tooth Abnormalities", "shortest_name_length": 74}
{"curie": "MONDO:0018878", "names": ["BOR", "bor", "bo syndrome", "BO syndrome", "Branchiootic syndrome", "branchiootic syndrome", "BRANCHIOOTIC DYSPLASIA", "branchiootic dysplasia", "Branchio-otic syndrome", "Branchiootic dysplasia", "Branchiootic syndrome (disorder)", "branchiootic syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "branchiootic syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C5554190", "names": ["SMARCA4-UT", "SMARCA4-Deficient Thoracic Sarcoma", "SMARCA4-deficient thoracic sarcoma", "SMARCA4-deficient sarcoma of thorax", "SMARCA4-Deficient Thoracic Sarcomatoid Tumor", "Thoracic SMARCA4-Deficient Undifferentiated Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SMARCA4-deficient thoracic sarcoma", "shortest_name_length": 10}
{"curie": "MONDO:0020134", "names": ["Posterior fossa cystic anomaly", "Cystic malformation of posterior fossa", "cystic malformation of the posterior fossa", "Cystic malformation of posterior fossa (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cystic malformation of the posterior fossa", "shortest_name_length": 30}
{"curie": "MONDO:0014570", "names": ["LCCS8", "LETHAL CONGENITAL CONTRACTURE SYNDROME 8", "lethal congenital contracture syndrome 8", "ADCY6 lethal congenital contracture syndrome", "lethal congenital contracture syndrome type 8", "lethal congenital contracture syndrome caused by mutation in ADCY6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal congenital contracture syndrome 8", "shortest_name_length": 5}
{"curie": "UMLS:C4727204", "names": ["Metastatic Soft Tissue Sarcoma, Excluding Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Soft Tissue Sarcoma, Excluding Liposarcoma", "shortest_name_length": 53}
{"curie": "MONDO:0022714", "names": ["PORC", "chester porphyria", "porphyria, Chester type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chester porphyria", "shortest_name_length": 4}
{"curie": "MONDO:0035743", "names": ["factor V amsterdam bleeding disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "factor V amsterdam bleeding disorder", "shortest_name_length": 36}
{"curie": "MONDO:0011607", "names": ["NRCLP2", "narcolepsy 2", "narcolepsy 2, susceptibility to", "NARCOLEPSY 2, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "narcolepsy 2, susceptibility to", "shortest_name_length": 6}
{"curie": "UMLS:C4687713", "names": ["Progressive Central Nervous System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Progressive Central Nervous System Neoplasm", "shortest_name_length": 43}
{"curie": "MONDO:0019808", "names": ["aortic atresia", "Aortic atresia", "Aortic valve atresia", "aortic valve atresia", "Aortic Valve Atresia", "atresia; aortic valve", "aortic valve; atresia", "Imperforate aortic valve", "aortic atresia (diagnosis)", "aortic valve atresia (disease)", "congenital aortic valve atresia", "Congenital Aortic Valve Atresia", "Congenital aortic valve atresia", "Congenital Atresia of Aortic Valve", "Congenital atresia of aortic valve", "congenital atresia of aortic valve", "Congenital atresia of aortic valve (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic valve atresia", "shortest_name_length": 14}
{"curie": "UMLS:C0279999", "names": ["recurrent adult NHL", "NHL, relapsed, adult", "NHL, recurrent, adult", "Recurrent Non-Hodgkin Lymphoma", "Recurrent Adult Non-Hodgkin Lymphoma", "recurrent adult non-Hodgkin lymphoma", "Adult Relapsed Non-Hodgkin's Lymphoma", "Relapsed Adult Non-Hodgkin's Lymphoma", "relapsed adult non-Hodgkin's lymphoma", "adult non-Hodgkin's lymphoma, relapsed", "Recurrent Adult Non-Hodgkin's Lymphoma", "Adult Recurrent Non-Hodgkin's Lymphoma", "adult non-Hodgkin's lymphoma, recurrent", "non-Hodgkin's lymphoma, relapsed, adult", "non-Hodgkin's lymphoma, recurrent, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Adult Non-Hodgkin Lymphoma", "shortest_name_length": 19}
{"curie": "MONDO:0019631", "names": ["PHPV", "PFVS", "PVPS", "ncRNA disease", "NCRNA disease", "Persistent Hyaloid Artery", "Persistent hyaloid artery", "Congenital retinal septum", "Persistent Hyaloid Arteries", "Persistent primary vitreous", "PERSISTENT FETAL VASCULATURE", "Persistent fetal vasculature", "Congenital retinal detachment", "congenital retinal detachment", "Persistent foetal vasculature", "Persistent Hyaloid Vasculature", "Persistent Hyaloid Vasculatures", "Persistent tunica vasculosa lentis", "Persistent hyaloid artery (disorder)", "Persistent Fetal Vasculature Syndrome", "persistent fetal vasculature syndrome", "Persistent fetal vasculature syndrome", "Persistent primary vitreous (disorder)", "Persistent foetal vasculature syndrome", "Remnants of the hyaloid vascular system", "Persistent hypertrophic primary vitreous", "persistent hyperplastic primary vitreous", "Persistent Hyperplastic Primary Vitreous", "Persistent hyperplastic primary vitreous", "PERSISTENT HYPERPLASTIC PRIMARY VITREOUS", "Persistent hyperplasia of primary vitreous", "non-syndromic congenital retinal non-attachment", "PHPV - Persistent hyperplastic primary vitreous", "Non-syndromic congenital retinal non-attachment", "Persistent hyperplastic primary vitreous (disorder)", "persistent hyperplastic primary vitreous (diagnosis)", "Persistent posterior fetal fibrovascular sheath of the lens", "Persistent posterior foetal fibrovascular sheath of the lens"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "persistent hyperplastic primary vitreous", "shortest_name_length": 4}
{"curie": "MONDO:0016412", "names": ["peripheral hypothyroidism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peripheral hypothyroidism", "shortest_name_length": 25}
{"curie": "MONDO:0019524", "names": ["Bartter syndrome type 4", "Bartter syndrome type IV", "Bartter's syndrome type 4", "Bartter syndrome type 4 (disorder)", "Bartter syndrome type 4 (diagnosis)", "Bartter syndrome with sensorineural deafness", "Bartter syndrome with sensorineural hearing loss"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bartter syndrome type 4", "shortest_name_length": 23}
{"curie": "MONDO:0010325", "names": ["Sdsx", "SDSX", "MRXSDS", "Stocco dos Santos syndrome", "mental retardation, Stocco dos Santos type", "Mental retardation, Stocco dos Santos type", "intellectual disability, Stocco dos Santos type", "Mental Retardation, X-Linked, Stocco Dos Santos Type", "mental retardation, X-linked, Stocco Dos Santos type", "mental retardation-hip luxation-G6PD variant syndrome", "STOCCO DOS SANTOS X-LINKED MENTAL RETARDATION SYNDROME", "Stocco DOS Santos X-linked mental retardation syndrome", "Stocco dos Santos X-linked mental retardation syndrome", "Stocco Dos Santos type X-linked intellectual disability", "X-linked intellectual disability Stocco Dos Santos type", "X-linked intellectual disability, Stocco dos Santos type", "X-linked intellectual disability, Stocco Dos Santos type", "intellectual disability, X-linked, Stocco Dos Santos type", "Stocco DOS Santos X-linked intellectual disability syndrome", "MENTAL RETARDATION, X-LINKED, SYNDROMIC, STOCCO DOS SANTOS TYPE", "X-linked intellectual disability Stocco Dos Santos type (disorder)", "X-linked intellectual disability Stocco Dos Santos type (diagnosis)", "intellectual developmental disorder, X-linked syndromic, Stocco dos Santos type", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, STOCCO DOS SANTOS TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability, Stocco dos Santos type", "shortest_name_length": 4}
{"curie": "MONDO:0008951", "names": ["CEREBROCORTICAL DEGENERATION OF INFANCY", "Cerebrocortical Degeneration of Infancy", "cerebrocortical degeneration of infancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebrocortical degeneration of infancy", "shortest_name_length": 39}
{"curie": "MONDO:0019795", "names": ["acrania", "Acrania", "Acranias", "acranius", "Acranius", "acalvaria", "Acalvaria", "Primary acalvaria", "primary acalvaria", "Acrania (disorder)", "Acraniate monster, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acalvaria", "shortest_name_length": 7}
{"curie": "MONDO:0033492", "names": ["CSS6", "Coffin-Siris syndrome 6", "ARID2-related BAFopathy", "COFFIN-SIRIS SYNDROME 6", "COFFIN-SIRIS syndrome 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Coffin-Siris syndrome 6", "shortest_name_length": 4}
{"curie": "MONDO:0010110", "names": ["TETAMS", "Zimmer phocomelia", "tetraamelia syndrome", "tetra-amelia syndrome", "Zimmer Taub Sova syndrome", "Tetraamelia multiple malformations", "TETRAAMELIA syndrome, autosomal recessive", "Tetraamelia multiple malformations X-linked", "Tetraamelia-multiple malformations syndrome", "tetraamelia-multiple malformations syndrome", "Tetraamelia with multiple malformation syndrome", "Tetra-amelia with multiple malformation syndrome", "Tetraamelia with multiple malformation syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tetraamelia-multiple malformations syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0007031", "names": ["familial abdominal aortic aneurysm", "Familial abdominal aortic aneurysm", "aortic aneurysm, familial abdominal", "hereditary abdominal aortic aneurysm", "Familial abdominal aortic aneurysm (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial abdominal aortic aneurysm", "shortest_name_length": 34}
{"curie": "UMLS:C2064242", "names": ["Anal Canal Undifferentiated Carcinoma", "undifferentiated carcinoma of anal canal", "undifferentiated carcinoma of anal canal (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "undifferentiated carcinoma of anal canal", "shortest_name_length": 37}
{"curie": "MONDO:0013832", "names": ["KTCN8", "keratoconus 8", "KERATOCONUS 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratoconus 8", "shortest_name_length": 5}
{"curie": "MONDO:0013933", "names": ["PBD5B", "peroxisome biogenesis disorder 5B", "Peroxisome Biogenesis Disorder 5B", "PEROXISOME BIOGENESIS DISORDER 5B", "peroxisome biogenesis disorder type 5B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder 5B", "shortest_name_length": 5}
{"curie": "UMLS:C1336814", "names": ["Transplant-Related Cancer", "Transplant-Related Malignancy", "Transplant-Related Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transplant-Related Malignant Neoplasm", "shortest_name_length": 25}
{"curie": "MONDO:0002518", "names": ["Gallbladder ICPN", "Gallbladder Papillomatosis", "gallbladder papillomatosis", "Intracystic Papillary Neoplasm", "gallbladder papillary neoplasm", "Gallbladder Papillary Neoplasm", "intracystic papillary neoplasm", "benign papillomatosis of gallbladder", "gall bladder papillary epithelial neoplasm", "Gallbladder Intracholecystic Papillary Neoplasm", "benign papillomatosis of gallbladder (diagnosis)", "Gallbladder Intracystic/Intaductal Papillary Neoplasm", "Gallbladder Intracholecystic Papillary (Tubular) Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gallbladder papillary neoplasm", "shortest_name_length": 16}
{"curie": "MONDO:0012762", "names": ["Cpvt2", "CPVT2", "VTSIP", "CVPT2", "Stress-induced polymorphic ventricular tachycardia", "ventricular tachycardia, stress-induced polymorphic", "VENTRICULAR TACHYCARDIA, STRESS-INDUCED POLYMORPHIC", "catecholaminergic polymorphic ventricular tachycardia 2", "ventricular tachycardia, catecholaminergic polymorphic, 2", "Ventricular Tachycardia, Catecholaminergic Polymorphic, 2", "VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 2", "CASQ2 catecholaminergic polymorphic ventricular tachycardia", "Catecholaminergic Polymorphic Ventricular Tachycardia Type 2", "catecholaminergic polymorphic ventricular tachycardia type 2", "ventricular tachycardia, catecholaminergic polymorphic, type 2", "catecholaminergic polymorphic ventricular tachycardia caused by mutation in CASQ2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "catecholaminergic polymorphic ventricular tachycardia 2", "shortest_name_length": 5}
{"curie": "UMLS:C0019207", "names": ["Morris Hepatoma", "Hepatoma, Morris"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatoma, Morris", "shortest_name_length": 15}
{"curie": "MONDO:0003035", "names": ["ovarian angiosarcoma", "Ovarian Angiosarcoma", "angiosarcoma of ovary", "Angiosarcoma of Ovary", "ovarian hemangiosarcoma", "Ovarian Hemangiosarcoma", "hemangiosarcoma of ovary", "hemangiosarcoma of Ovary", "Hemangiosarcoma of Ovary", "angiosarcoma of the ovary", "Angiosarcoma of the Ovary", "ovary angiosarcoma (disease)", "Hemangiosarcoma of the Ovary", "hemangiosarcoma of the ovary", "angiosarcoma (disease) of ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian angiosarcoma", "shortest_name_length": 20}
{"curie": "UMLS:C1332527", "names": ["Benign Ovarian Serous Tumor", "Benign Ovarian Serous Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Ovarian Serous Tumor", "shortest_name_length": 27}
{"curie": "MONDO:0005952", "names": ["Scarlatina", "Scarletina", "SCARLATINA", "scarlatina", "febris; rubra", "scarlet fever", "rubra; febris", "Scarlet Fever", "Scarlet fever", "SCARLET FEVER", "Scarlet Fevers", "Fever, Scarlet", "Fevers, Scarlet", "Scarlet fever, NOS", "Scarlet fever (disorder)", "scarlet fever (diagnosis)", "Streptococcal sore throat with scarlatina", "Streptococcal sore throat and scarlet fever", "Streptococcal sore throat with scarlatina (disorder)", "Streptococcal sore throat with scarlatina (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scarlet fever", "shortest_name_length": 10}
{"curie": "UMLS:C5667584", "names": ["Non-Pontine-DMG", "Diffuse Non-Pontine Midline Glioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse Non-Pontine Midline Glioma", "shortest_name_length": 15}
{"curie": "MONDO:0012209", "names": ["Mégarbané-Loiselet syndrome", "Megarbane Loiselet syndrome", "MC)garbanC)-Loiselet syndrome", "branchiogenic deafness syndrome", "BRANCHIOGENIC-DEAFNESS SYNDROME", "Branchiogenic-Deafness Syndrome", "Branchiogenic deafness syndrome", "BRANCHIOGENIC-deafness syndrome", "Branchiogenic hearing loss syndrome", "Branchiogenic deafness syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "branchiogenic deafness syndrome", "shortest_name_length": 27}
{"curie": "MONDO:0021812", "names": ["Cylindroma", "cylindroma", "Turban tumor", "Turban tumour", "Spiegler's tumor", "Dermal Cylindroma", "dermal cylindroma", "Spiegler's tumour", "Dermal cylindroma", "cylindroma of skin", "Cylindroma of skin", "Cylindroma of Skin", "cylindroma of the skin", "Cylindroma of the Skin", "Eccrine dermal cylindroma", "Eccrine dermal cylindroma of skin", "adnexal sweat gland spiradenoma/cylindroma", "Cylindroma of skin (morphologic abnormality)", "Eccrine dermal cylindroma of skin (disorder)", "adnexal spiradenoma/cylindroma of a sweat gland", "Eccrine dermal cylindroma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adnexal spiradenoma/cylindroma of a sweat gland", "shortest_name_length": 10}
{"curie": "MONDO:0015856", "names": ["syndromic breast hypoplasia/aplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic breast hypoplasia/aplasia", "shortest_name_length": 35}
{"curie": "UMLS:C1333021", "names": ["Chondrosarcoma NCI Grade 1", "Chondrosarcoma NCI Grade I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chondrosarcoma NCI Grade 1", "shortest_name_length": 26}
{"curie": "MONDO:0011847", "names": ["MGOA", "MGR4", "common migraine", "migraine without aura, susceptibility to, 4", "MIGRAINE WITHOUT AURA, SUSCEPTIBILITY TO, 4", "migraine without aura, susceptibility to, type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "migraine without aura, susceptibility to, 4", "shortest_name_length": 4}
{"curie": "UMLS:C3887633", "names": ["Familial Dandy-Walker Syndrome", "Dandy Walker Syndrome, Familial", "Dandy-Walker Syndrome, Familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dandy-Walker Syndrome, Familial", "shortest_name_length": 30}
{"curie": "MONDO:0002167", "names": ["Rectal Melanoma", "rectal melanoma", "rectum melanoma", "Melanoma of Rectum", "melanoma of rectum", "Melanoma of the Rectum", "melanoma of the rectum", "Cancer rectum melanoma", "rectal malignant melanoma", "rectum melanoma (disease)", "Rectal Malignant Melanoma", "rectum malignant melanoma", "malignant melanoma of rectum", "Malignant melanoma of rectum", "Malignant Melanoma of Rectum", "melanoma (disease) of rectum", "Malignant Melanoma of the Rectum", "malignant melanoma of the rectum", "Malignant melanoma of rectum (disorder)", "malignant melanoma of rectum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rectum malignant melanoma", "shortest_name_length": 15}
{"curie": "MONDO:0600030", "names": ["B-ALL with TCF3-PBX1", "B-lymphoblastic leukemia/lymphoma with TCF3-PBX1", "B-lymphoblastic leukemia/lymphoma with t(1;19)(q23;p13.3)", "B-lymphoblastic leukemia/lymphoma with t(1;19)(q23;p13.3);TCF3-PBX1", "B-Acute Lymphoblastic Leukemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1)", "B Acute Lymphoblastic Leukemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1)", "B-acute lymphoblastic leukemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1)", "B acute lymphoblastic leukemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1)", "B lymphoblastic leukemia lymphoma with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1)", "B Lymphoblastic Leukemia/Lymphoma with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1)", "B-Lymphoblastic Leukemia/Lymphoma with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1)", "B lymphoblastic leukemia lymphoma with t(1;19)(Q23;P13.3); E2A-PBX1 (TCF3/PBX1)", "B lymphoblastic leukemia/lymphoma with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1)", "B lymphoblastic leukaemia lymphoma with t(1;19)(Q23;P13.3); E2A-PBX1 (TCF3/PBX1)", "B lymphoblastic leukaemia lymphoma with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1)", "B lymphoblastic leukemia lymphoma with t(1;19) (q23;p.13.3); E2A-PBX1 (TCF3/PBX1)", "B-cell acute lymphoblastic leukemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1)", "B-Cell Acute Lymphoblastic Leukemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1)", "B lymphoblastic leukemia lymphoma with t(1;19)(Q23;P13.3); E2A-PBX1 (TCF3/PBX1) (disorder)", "B lymphoblastic leukemia lymphoma with t(1;19) (q23;p.13.3); E2A-PBX1 (TCF3/PBX1) (diagnosis)", "B lymphoblastic leukemia lymphoma with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1) (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-cell acute lymphoblastic leukemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1)", "shortest_name_length": 20}
{"curie": "UMLS:C4526717", "names": ["Stage IB", "Stage IB Lung Cancer", "Stage IB Lung Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Lung Cancer AJCC v8", "shortest_name_length": 8}
{"curie": "MONDO:0015229", "names": ["BBS", "Biedl-Bardet", "bardet biedl syndrome", "bardet-biedl syndrome", "BARDET-BIEDL SYNDROME", "Bardet Biedl Syndrome", "Biedl-Bardet syndrome", "Bardet-Biedl syndrome", "Bardet-Biedl Syndrome", "Syndrome, Bardet-Biedl", "Laurence-Moon Syndrome", "Bardet-Biedl syndrome (BBS)", "Laurence-Moon-Biedl Syndrome", "Bardet-Biedl syndrome (disorder)", "Laurence Moon Bardet Biedl Syndrome", "Laurence-Moon-Bardet-Biedl Syndrome", "Laurence-Moon-Bardet-Biedl syndrome", "Syndrome, Laurence-Moon-Bardet-Biedl", "Laurence-Moon (-Bardet)-Biedl syndrome", "LMBB - Laurence-Moon-Bardet-Biedl syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bardet-Biedl syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C5667309", "names": ["Recurrent HER2-Positive Breast Carcinoma", "Recurrent HER2 Positive Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent HER2-Positive Breast Carcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0010389", "names": ["IMD34", "AMCBX2", "IMMUNODEFICIENCY 34", "immunodeficiency 34", "immunodeficiency type 34", "X-linked MSMD due to CYBB deficiency", "familial atypical mycobacteriosis X-linked 2", "ATYPICAL MYCOBACTERIOSIS, FAMILIAL, X-LINKED 2", "atypical Mycobacteriosis, familial, X-linked 2", "Atypical Mycobacteriosis, Familial, X-Linked 2", "immunodeficiency 34, mycobacteriosis, X-linked", "immunodeficiency 34, Mycobacteriosis, X-linked", "IMMUNODEFICIENCY 34, MYCOBACTERIOSIS, X-LINKED", "Atypical Mycobacterial Infection, Disseminated, X-Linked 2", "CYBB X-linked mendelian susceptibility to mycobacterial diseases", "immunodeficiency 34, mycobacteriosis, X-linked, X-linked recessive", "Atypical Mycobacterial Infection, Familial Disseminated, X-Linked 2", "X-linked Mendelian susceptibility to mycobacterial diseases due to CYBB deficiency", "X-linked mendelian susceptibility to mycobacterial diseases due to CYBB deficiency", "X-linked mendelian susceptibility to mycobacterial diseases caused by mutation in CYBB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked Mendelian susceptibility to mycobacterial diseases due to CYBB deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C5557382", "names": ["Female Reproductive System Smooth Muscle Tumor of Uncertain Malignant Potential", "Female Reproductive System Smooth Muscle Neoplasm of Uncertain Malignant Potential"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Female Reproductive System Smooth Muscle Tumor of Uncertain Malignant Potential", "shortest_name_length": 79}
{"curie": "MONDO:0022735", "names": ["Choroid Plexus Cyst", "choroid plexus cyst", "Choroid plexus cyst", "choroid cyst plexus", "choroid cysts plexus", "Choroid plexus cysts", "choroid plexus; cyst", "cyst; choroid plexus", "Cyst of Choroid Plexus", "plexus choroideus; cyst", "CPC - choroid plexus cyst", "CPC - Choroid plexus cyst", "Choroid Plexus Pseudocyst", "Cyst of the Choroid Plexus", "Choroid plexus cyst (disorder)", "choroid plexus cyst (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choroid plexus cyst", "shortest_name_length": 19}
{"curie": "MONDO:0024971", "names": ["Milk fever", "milk fever", "Animal Milk Fever", "animal milk fever", "Milk Fever, Animal", "Parturient Pareses", "parturient Pareses", "Parturient Paresis", "fever, animal milk", "Fever, Animal Milk", "milk fever, animal", "Parturient paresis", "parturient paresis", "paresis, parturient", "Paresis, Parturient", "Pareses, Parturient", "Pareses, parturient", "Milk fever in animals", "Bovine parturient hypocalcemia", "Bovine parturient hypocalcaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parturient paresis", "shortest_name_length": 10}
{"curie": "UMLS:C1335750", "names": ["Renal Fibroepithelial Polyp", "Kidney Fibroepithelial Polyp", "Fibroepithelial Polyp of Kidney", "Renal Pelvis Fibroepithelial Polyp", "Fibroepithelial Polyp of the Kidney", "Kidney Pelvis Fibroepithelial Polyp", "Fibroepithelial Polyp of Renal Pelvis", "Fibroepithelial Polyp of Kidney Pelvis", "Fibroepithelial Polyp of the Renal Pelvis", "Fibroepithelial Polyp of the Kidney Pelvis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal Pelvis Fibroepithelial Polyp", "shortest_name_length": 27}
{"curie": "MONDO:0035706", "names": ["SETD2-related microcephaly-severe intellectual disability-multiple congenital anomalies syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SETD2-related microcephaly-severe intellectual disability-multiple congenital anomalies syndrome", "shortest_name_length": 96}
{"curie": "UMLS:C0021167", "names": ["Incontinence", "INCONTINENCE", "incontinence", "incontinences", "INCONTINENCE NOS", "Incontinence NOS", "Incontinence, NOS", "Incontinence (finding)", "Urinary/Bowel incontinence", "Incontinence (excluding P12)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Incontinence", "shortest_name_length": 12}
{"curie": "MONDO:0020602", "names": ["SDYS", "DGSX", "Sgbs", "SGBS", "SGBS1", "SGB syndrome", "Simpson syndrome", "Bulldog syndrome", "Simpson Syndrome", "bulldog syndrome", "BULLDOG SYNDROME", "Sara Angers syndrome", "Golabi-Rosen syndrome", "GOLABI-ROSEN SYNDROME", "DGSX Golabi-Rosen syndrome", "Simpson Dysplasia Syndrome", "Simpson dysmorphia syndrome", "SIMPSON DYSMORPHIA SYNDROME", "Simpson-Golabi-Behmel syndrome", "GPC3 Simpson-Golabi-Behmel syndrome", "X-linked dysplasia gigantism syndrome", "Simpson Golabi Behmel Syndrome Type 1", "Simpson-Golabi-Behmel syndrome type 1", "Simpson-Golabi-Behmel syndrome, type 1", "Simpson-Golabi-Behmel Syndrome, Type 1", "SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1", "DYSPLASIA GIGANTISM SYNDROME, X-LINKED", "Dysplasia gigantism syndrome, X-linked", "Mental Retardation-Overgrowth Syndrome", "dysplasia gigantism syndrome, X-linked", "Simpson-Golabi-Behmel syndrome caused by mutation in GPC3", "Simpson-Golabi-Behmel syndrome, type 1, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Simpson-Golabi-Behmel syndrome type 1", "shortest_name_length": 4}
{"curie": "UMLS:C0751861", "names": ["Childhood Neurologic Saturnism", "Saturnism, Childhood Neurologic", "Plumbism, Neurologic, Childhood", "Neurologic Saturnism, Childhood", "Lead Poisoning, Neurologic, Childhood", "Poisoning, Lead, Neurologic, Childhood", "Neurotoxicity Syndrome, Lead, Childhood", "Nervous System Poisoning, Lead, Childhood", "Lead Poisoning, Nervous System, Childhood", "Poisoning, Lead, Nervous System, Childhood", "Lead-Induced Nervous System Disease, Childhood", "Lead Induced Nervous System Disease, Childhood", "Nervous System Disease, Lead-Induced, Childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lead Poisoning, Nervous System, Childhood", "shortest_name_length": 30}
{"curie": "MONDO:0005979", "names": ["TOS", "outlet syndrome thoracic", "THORACIC OUTLET SYNDROME", "Thoracic outlet syndrome", "thoracic outlet syndrome", "Thoracic Outlet Syndrome", "thoracic outlet syndromes", "outlet syndromes thoracic", "Thoracic Outlet Syndromes", "Outlet Syndrome, Thoracic", "Syndrome, Thoracic Outlet", "thoracic outlet; syndrome", "syndrome; thoracic outlet", "Syndromes, Thoracic Outlet", "outlet; thoracic, syndrome", "Outlet Syndromes, Thoracic", "TOS - Thoracic outlet syndrome", "TOS - thoracic outlet syndrome", "CERVICOTHORACIC OUTLET SYNDROME", "cervicothoracic outlet; syndrome", "syndrome; cervicothoracic outlet", "Aperture Syndrome, Thoracic Outlet", "Thoracic outlet syndrome (disorder)", "Superior Thoracic Aperture Syndrome", "Thoracic outlet compression syndrome", "thoracic outlet syndrome (diagnosis)", "thoracic outlet compression syndrome", "Thoracic Outlet Neurovascular Syndrome", "Neurovascular Syndrome, Thoracic Outlet"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thoracic outlet syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0000230", "names": ["Israeli tick typhus", "Israeli spotted fever"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Israeli tick typhus", "shortest_name_length": 19}
{"curie": "MONDO:0043537", "names": ["Horton", "red migraine", "Horton headache", "Horton Syndrome", "Horton syndrome", "horton syndrome", "HORTON SYNDROME", "syndrome, Horton", "Cluster headache", "hortons syndrome", "cluster migraine", "cluster headache", "Headache;cluster", "Hortons syndrome", "headache cluster", "CLUSTER HEADACHE", "Syndrome, Horton", "Hortons Syndrome", "Cluster Headache", "HEADACHE CLUSTER", "Horton's syndrome", "ciliary neuralgia", "Cluster headaches", "cluster headaches", "Horton's headache", "headaches cluster", "clusters headache", "HORTON'S HEADACHE", "headache; cluster", "Ciliary neuralgia", "horton's syndrome", "CLUSTER HEADACHES", "cluster; headache", "Ciliary Neuralgia", "horton's headache", "headache, cluster", "Cluster Headaches", "Horton's Syndrome", "Headache, Cluster", "Headaches cluster", "vasomotor headache", "Headache histamine", "HEADACHE HISTAMINE", "neuralgia; ciliary", "histamine headache", "headaches, cluster", "Headache vasomotor", "Neuralgic migraine", "ciliary; neuralgia", "Headaches, Cluster", "Neuralgia, Ciliary", "HEADACHE VASOMOTOR", "syndrome, Horton's", "horton's neuralgia", "Horton's neuralgia", "Ciliary Neuralgias", "neuralgia, ciliary", "neuralgic migraine", "ciliary neuralgias", "HISTAMINE HEADACHE", "Neuralgic Migraine", "headache histamine", "Histamine headache", "ERYTHROPROSOPALGIA", "Syndrome, Horton's", "Vasomotor headache", "neuralgic migraines", "migraine, neuralgic", "Neuralgic Migraines", "Histamine cephalgia", "Histamine Cephalgia", "histamine; headache", "histamine cephalgia", "Migraine, Neuralgic", "beuralgias, ciliary", "headaches histamine", "headache; histamine", "Neuralgias, Ciliary", "migraines, neuralgic", "Histamine Cephalgias", "Cluster headache NOS", "histamine cephalgias", "Cephalgia, histamine", "migrainous neuralgia", "BING-HORTON SYNDROME", "Migrainous neuralgia", "Migraines, Neuralgic", "Cephalgia, Histamine", "migrainous; neuralgia", "Cephalgias, Histamine", "Cephalgias, histamine", "neuralgia; migrainous", "CEPHALALGIA, HISTAMINE", "cluster headache chronic", "Chronic Cluster Headache", "chronic cluster headache", "Chronic cluster headache", "Cluster Headache Syndrome", "cluster headache, chronic", "Cluster headache syndrome", "chronic cluster headaches", "Chronic Cluster Headaches", "Headache, Chronic Cluster", "episodic cluster headache", "cluster headache syndrome", "headache, chronic cluster", "Cluster Headache, Chronic", "atypical cluster headache", "headache syndrome, cluster", "headache, episodic cluster", "headaches, chronic cluster", "syndrome, cluster headache", "cluster headaches, chronic", "cluster; headache syndrome", "syndrome; cluster headache", "Syndrome, Cluster Headache", "Headaches, Chronic Cluster", "headache, atypical cluster", "cluster headache, atypical", "erythroprosopalgia of bing", "Cluster Headaches, Chronic", "atypical cluster headaches", "episodic cluster headaches", "cluster headache syndromes", "cluster headache, episodic", "Headache Syndrome, Cluster", "Cluster Headache Syndromes", "headache syndromes, cluster", "Syndromes, Cluster Headache", "Ciliary neuralgia (finding)", "Headache Syndromes, Cluster", "headaches, episodic cluster", "erythromelalgia of the head", "headaches, atypical cluster", "cluster headaches, episodic", "syndromes, cluster headache", "cluster headaches, atypical", "Chronic cluster headache NOS", "cluster headache (diagnosis)", "Cluster headache syndrome NOS", "Chronic cluster headache (disorder)", "chronic cluster headache (diagnosis)", "Cluster headache syndrome (disorder)", "Cluster headache syndrome, unspecified", "CEPHALALGIA, PAROXYSMAL, NOCTURNAL, ORBITAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cluster headache syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0007732", "names": ["HOS", "Hos1", "HOS1", "HOS 1", "Holt-Oram", "holt oram syndrome", "HOLT-Oram syndrome", "Holt-Oram Syndrome", "holt-oram syndrome", "Holt Oram syndrome", "Holt-Oram syndrome", "HOLT-ORAM SYNDROME", "heart-hand syndrome", "HEART-HAND SYNDROME", "Heart-hand syndrome", "Cardiac-limb syndrome", "Cardiac-Limb Syndrome", "Atrio-Digital Syndrome", "atrio digital syndrome", "atriodigital dysplasia", "atrio-digital syndrome", "ATRIODIGITAL DYSPLASIA", "Atriodigital dysplasia", "Atrio-digital syndrome", "Ventriculo-Radial Syndrome", "heart-hand syndrome type 1", "Heart-hand syndrome type 1", "ventriculo-radial syndrome", "heart-hand syndrome, type 1", "Heart-Hand Syndrome, Type 1", "Atriodigital dysplasia type 1", "atriodigital dysplasia type 1", "Holt-Oram syndrome (disorder)", "Holt-Oram syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Holt-Oram syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C1707377", "names": ["Chest Wall Hamartoma", "Chest Wall Chondromesenchymal Hamartoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chest Wall Chondromesenchymal Hamartoma", "shortest_name_length": 20}
{"curie": "UMLS:C0520599", "names": ["NEONATAL HYPOXIA", "hypoxia neonatal", "neonatal hypoxia", "Neonatal hypoxia", "hypoxia neonatorum", "hypoxia of newborn", "Neonatal hypoxia, NOS", "Hypoxia NOS of newborn", "Hypoxia of newborn NOS", "Hypoxia, in liveborn infant", "Neonatal oxygen desaturation", "hypoxia of newborn (diagnosis)", "Hypoxia, NOS, in liveborn infant", "Hypoxia, in liveborn infant (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypoxia, in liveborn infant", "shortest_name_length": 16}
{"curie": "UMLS:C0271547", "names": ["Hypersomatotropism", "Growth hormone overproduction", "growth hormone; overproduction", "overproduction; growth hormone", "Overproduction of growth hormone", "Overproduction of growth hormone, NOS", "Overproduction of growth hormone (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Overproduction of growth hormone", "shortest_name_length": 18}
{"curie": "MONDO:0002032", "names": ["Colon Cancer", "colon cancer", "Carcinoma;colon", "Colon Carcinoma", "Carcinoma colon", "carcinoma colon", "CARCINOMA COLON", "colon carcinoma", "COLON CARCINOMA", "Colon carcinoma", "COLON, CARCINOMA", "Colonic carcinoma", "Colonic Carcinoma", "colonic carcinoma", "carcinoma of colon", "CARCINOMA OF COLON", "Carcinoma of colon", "Carcinoma of Colon", "bowel carcinoma large", "carcinoma colon cancer", "Carcinoma of the Colon", "carcinoma of the colon", "COLON CANCER, CARCINOMA", "carcinoma intestine large", "Carcinoma of colon (disorder)", "Carcinoma of colon (diagnosis)", "large intestine malignant carcinoma of colon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colon carcinoma", "shortest_name_length": 12}
{"curie": "UMLS:C3899171", "names": ["FGFR3 Chondrodysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FGFR3 Chondrodysplasia", "shortest_name_length": 22}
{"curie": "UMLS:C1504321", "names": ["Infantile spitting up"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infantile spitting up", "shortest_name_length": 21}
{"curie": "UMLS:C0006902", "names": ["capillaritis", "Capillaritis", "Capillaritis, NOS", "Capillaritis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Capillaritis", "shortest_name_length": 12}
{"curie": "UMLS:C5419506", "names": ["Progesterone Receptor Expressing Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Progesterone Receptor Expressing Malignant Neoplasm", "shortest_name_length": 51}
{"curie": "UMLS:C0279636", "names": ["M2 Childhood AGL", "M2 Pediatric AGL", "pediatric acute M2 leukemia", "Childhood Acute M2 Leukemia", "Pediatric Acute M2 Leukemia", "childhood acute M2 leukemia", "M2 leukemia, childhood acute", "Pediatric AGL with Maturation", "childhood AML with maturation", "M2 childhood AML with maturation", "M2 Childhood Acute Myelogenous Leukemia", "M2 Pediatric Acute Myelogenous Leukemia", "Acute Myeloid Leukemia (AML) with Maturation", "Pediatric Acute Myeloid Leukemia with Maturation", "Childhood Acute Myeloid Leukemia with Maturation", "Pediatric Acute Myelocytic Leukemia with Maturation", "M2 Pediatric Acute Myeloid Leukemia with Maturation", "Childhood Acute Myelocytic Leukemia with Maturation", "M2 Childhood Acute Myeloid Leukemia with Maturation", "Childhood Acute Myelogenous Leukemia with Maturation", "Pediatric Acute Myelogenous Leukemia with Maturation", "Childhood Acute Myeloblastic Leukemia with Maturation", "Pediatric Acute Myeloblastic Leukemia with Maturation", "Childhood Acute Granulocytic Leukemia with Maturation", "Pediatric Acute Granulocytic Leukemia with Maturation", "pediatric acute myeloblastic leukemia with maturation", "M2 Childhood Acute Myelocytic Leukemia with Maturation", "M2 Pediatric Acute Myelocytic Leukemia with Maturation", "M2 Pediatric Acute Myelogenous Leukemia with Maturation", "M2 Childhood Acute Myelogenous Leukemia with Maturation", "M2 Pediatric Acute Granulocytic Leukemia with Maturation", "M2 Pediatric Acute Myeloblastic Leukemia with Maturation", "M2 childhood acute myeloblastic leukemia with maturation", "M2 Childhood Acute Myeloblastic Leukemia with Maturation", "Childhood Acute Myeloblastic Leukemia with Maturation (M2)", "childhood acute myeloblastic leukemia with maturation (M2)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Acute Myeloid Leukemia with Maturation", "shortest_name_length": 16}
{"curie": "MONDO:0014970", "names": ["SPGF17", "PLCZ1 azoospermia", "spermatogenic failure 17", "SPERMATOGENIC FAILURE 17", "spermatogenic failure type 17", "spermatogenic failure 17; SPGF17", "azoospermia caused by mutation in PLCZ1", "Male infertility due to oocyte Activation failure", "MALE INFERTILITY DUE TO OOCYTE ACTIVATION FAILURE", "Male infertility due to oocyte activation failure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 17", "shortest_name_length": 6}
{"curie": "MONDO:0032706", "names": ["SCAR27", "autosomal recessive spinocerebellar ataxia 27", "spinocerebellar ataxia, autosomal recessive 27", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 27"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia, autosomal recessive 27", "shortest_name_length": 6}
{"curie": "UMLS:C1333319", "names": ["Breast Ductal Carcinoma with Squamous Metaplasia", "Ductal Breast Carcinoma with Squamous Metaplasia", "Ductal Carcinoma of Breast with Squamous Metaplasia", "Ductal Carcinoma of the Breast with Squamous Metaplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Ductal Carcinoma with Squamous Metaplasia", "shortest_name_length": 48}
{"curie": "UMLS:C5418908", "names": ["Resectable Malignant Female Reproductive System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Malignant Female Reproductive System Neoplasm", "shortest_name_length": 56}
{"curie": "UMLS:C4526840", "names": ["Bone Sarcoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone Sarcoma by AJCC v7 Stage", "shortest_name_length": 29}
{"curie": "MONDO:0004755", "names": ["Monieziases", "Monieziasis", "monieziasis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "monieziasis", "shortest_name_length": 11}
{"curie": "MONDO:0000424", "names": ["hypocobalaminemia", "cobalamin deficiency", "vitamin B12 deficiency", "inborn vitamin B12 deficiency", "inborn vitamin B12 deficiency (disease)", "inborn cobalamin metabolic process disorder", "inborn error of cobalamin metabolic process", "rare inborn error of cobalamin metabolic process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn vitamin B12 deficiency", "shortest_name_length": 17}
{"curie": "MONDO:0015417", "names": ["Tessier number 6 facial cleft"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tessier number 6 facial cleft", "shortest_name_length": 29}
{"curie": "UMLS:C0857836", "names": ["JCV Infection", "JC Virus Infection", "JC virus infection", "JC Polyomavirus Infection", "Polyomavirus JC Infection", "John Cunningham Virus Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "JC virus infection", "shortest_name_length": 13}
{"curie": "UMLS:C4525727", "names": ["Cortical Cataract Grade 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cortical Cataract Grade 1", "shortest_name_length": 25}
{"curie": "UMLS:C0752179", "names": ["Herpes zoster meningoencephalitis", "Herpes Zoster Meningoencephalitis", "Meningoencephalitis, Herpes Zoster", "herpes; meningoencephalitis, h.zoster (etiology)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meningoencephalitis, Herpes Zoster", "shortest_name_length": 33}
{"curie": "UMLS:C0686510", "names": ["Carcinoma in situ of adrenal cortex", "Carcinoma in situ of adrenal cortex (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carcinoma in situ of adrenal cortex", "shortest_name_length": 35}
{"curie": "UMLS:C4725858", "names": ["Recurrent Dedifferentiated Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Dedifferentiated Liposarcoma", "shortest_name_length": 38}
{"curie": "UMLS:C4553783", "names": ["stage 0a ureter cancer", "Stage 0a Ureter Cancer", "stage 0a ureter cancer AJCC v8", "Stage 0a Ureter Cancer AJCC v8", "stage 0a ureter urothelial carcinoma AJCC v8", "Stage 0a Ureter Urothelial Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0a Ureter Cancer AJCC v8", "shortest_name_length": 22}
{"curie": "MONDO:0007300", "names": ["Cerebral sarcoma", "cerebral sarcoma", "CEREBRAL SARCOMA", "telencephalon sarcoma", "sarcoma of telencephalon", "Familial cerebral sarcomas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral sarcoma", "shortest_name_length": 16}
{"curie": "UMLS:C1504422", "names": ["Application site hypersensitivity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Application site hypersensitivity", "shortest_name_length": 33}
{"curie": "MONDO:0013777", "names": ["PHA2B", "pseudohypoaldosteronism type 2B", "Pseudohypoaldosteronism type 2B", "pseudohypoaldosteronism, type 2B", "PSEUDOHYPOALDOSTERONISM, TYPE IIB", "Pseudohypoaldosteronism, Type IIb", "pseudohypoaldosteronism, type IIB", "WNK4 pseudohypoaldosteronism type 2", "pseudohypoaldosteronism type 2 caused by mutation in WNK4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudohypoaldosteronism type 2B", "shortest_name_length": 5}
{"curie": "UMLS:C4688346", "names": ["Advanced B-Cell Neoplasm", "Advanced B-Cell Malignancy", "Advanced B-Cell Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced B-Cell Malignant Neoplasm", "shortest_name_length": 24}
{"curie": "UMLS:C2981385", "names": ["Stage IIA Appendix Cancer", "Stage IIA Appendix Carcinoma", "Stage IIA Appendix Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Appendix Carcinoma AJCC v7", "shortest_name_length": 25}
{"curie": "UMLS:C0410959", "names": ["Fetal Acidemia", "Fetal Acidosis", "Fetal acidosis", "Foetal acidosis", "Fetal acidosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fetal acidosis", "shortest_name_length": 14}
{"curie": "UMLS:C1335693", "names": ["Relapsed Anaplastic Large Cell Lymphoma", "Recurrent Anaplastic Large Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Anaplastic Large Cell Lymphoma", "shortest_name_length": 39}
{"curie": "MONDO:0030999", "names": ["NEDCAFD", "NEURODEVELOPMENTAL DISORDER WITH CEREBRAL ATROPHY AND VARIABLE FACIAL DYSMORPHISM", "neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism", "shortest_name_length": 7}
{"curie": "MONDO:0005643", "names": ["Alphavirus disease", "Alphavirus Infection", "alphavirus infections", "Infection, Alphavirus", "Alphavirus Infections", "Alpha Virus Infection", "Infections, Alphavirus", "Virus Infection, Alpha", "Alpha Virus Infections", "Disease due to Alphavirus", "DISEASES DUE TO ALPHAVIRUS", "Disease caused by Alphavirus", "Alphavirus infectious disease", "Alphavirus disease or disorder", "Disease due to Alphavirus, NOS", "Alphavirus caused disease or disorder", "Disease caused by Alphavirus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alphavirus infectious disease", "shortest_name_length": 18}
{"curie": "MONDO:0000703", "names": ["collagenous colitis", "COLLAGENOUS COLITIS", "colitis collagenous", "Collagenous colitis", "Colitis collagenous", "Collagenous Colitis", "Colitis, Collagenous", "CC - Collagenous colitis", "Collagenous colitis (disorder)", "collagenous colitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "collagenous colitis", "shortest_name_length": 19}
{"curie": "UMLS:C5205059", "names": ["Recurrent Transformed Follicular Lymphoma to Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Transformed Follicular Lymphoma to Diffuse Large B-Cell Lymphoma", "shortest_name_length": 74}
{"curie": "MONDO:0032692", "names": ["GAMOS7", "GALLOWAY-MOWAT SYNDROME 7", "Galloway-Mowat syndrome 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Galloway-Mowat syndrome 7", "shortest_name_length": 6}
{"curie": "UMLS:C0750986", "names": ["Internal Carotid Artery Disease", "Internal Carotid Artery Diseases", "Arterial Diseases, Internal Carotid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Internal Carotid Artery Diseases", "shortest_name_length": 31}
{"curie": "MONDO:0009504", "names": ["MTDPS9", "fatal infantile lactic acidosis", "succinate-CoA ligase deficiency", "Lactic Acidosis, Fatal Infantile", "lactic acidosis, fatal infantile", "lactic acidosis congenital infantile", "Lactic acidosis congenital infantile", "Mitochondrial DNA Depletion Syndrome-9", "mitochondrial DNA depletion syndrome 9", "lactic acidosis, fatal infantile, formerly", "LACTIC ACIDOSIS, FATAL INFANTILE, FORMERLY", "SUCLG1 mitochondrial DNA depletion syndrome", "mitochondrial DNA depletion syndrome type 9", "Fatal infantile lactic acidosis with methylmalonic aciduria", "fatal infantile lactic acidosis with methylmalonic aciduria", "mitochondrial DNA depletion syndrome caused by mutation in SUCLG1", "Fatal infantile lactic acidosis co-occurrent with methylmalonic aciduria", "Fatal infantile lactic acidosis co-occurrent with methylmalonic aciduria (disorder)", "mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)", "MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITH METHYLMALONIC ACIDURIA)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial DNA depletion syndrome 9", "shortest_name_length": 6}
{"curie": "UMLS:C1963650", "names": ["pharynx necrosis", "pharynx; necrosis", "necrosis; pharynx", "Pharyngeal necrosis", "pharyngeal necrosis", "Pharyngeal Necrotic Lesion", "pharyngeal necrosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pharynx necrosis", "shortest_name_length": 16}
{"curie": "MONDO:0004975", "names": ["AD", "DAT", "SDAT", "dats", "Alzheimer", "Senile Dementia", "senile dementia", "Dementia, Senile", "ALZHEIMER DISEASE", "Alzheimer disease", "Alzheimer Disease", "Alzheimers Disease", "alzheimer diseases", "Alzheimer Diseases", "Disease;Alzheimers", "Alzheimers disease", "Alzheimer Dementia", "Alzheimer syndrome", "Alzheimer Syndrome", "Alzheimer dementia", "DEMENTIA ALZHEIMER", "alzheimers disease", "alzheimers dementia", "Alzheimers dementia", "Dementia, Alzheimer", "Alzheimer Sclerosis", "Alzheimers Diseases", "Alzheimer Dementias", "dementia alzheimers", "Alzheimer sclerosis", "Alzheimer's disease", "alzheimer's disease", "ALZHEIMER'S DISEASE", "Alzheimer's Disease", "alzheimer's diseases", "Alzheimer's Diseases", "Alzheimer's dementia", "Sclerosis, Alzheimer", "Alzheimer; sclerosis", "Alzheimer's Dementia", "sclerosis; Alzheimer", "simple senile dementia", "Alzheimer disease (AD)", "Alzheimer dementia (AD)", "Alzheimer Type Dementia", "Alzheimer-type dementia", "Alzheimer's disease, NOS", "AD - Alzheimer's disease", "Dementia, Alzheimer Type", "Dementia Alzheimer's type", "Dementia of Alzheimers Type", "Alzheimer disease, familial", "obsolete_Alzheimer's disease", "Alzheimer-Type Dementia (ATD)", "presenile and senile dementia", "Alzheimer Type Dementia (ATD)", "Alzheimer disease (diagnosis)", "Alzheimer-type dementia (ADT)", "Dementia, Alzheimer-Type (ATD)", "Alzheimer's disease (disorder)", "Alzheimer; dementia (etiology)", "dementia; Alzheimer (etiology)", "dementia of the Alzheimer type", "DEMENTIA OF THE ALZHEIMER TYPE", "Alzheimer Type Senile Dementia", "DAT - Dementia Alzheimer's type", "Dementia in Alzheimer's disease", "Senile Dementia, Alzheimer Type", "Alzheimer's disease, unspecified", "Dementia of the Alzheimer's type", "dementia; Alzheimer (manifestation)", "Alzheimer; dementia (manifestation)", "Primary Senile Degenerative Dementia", "dementia of the Alzheimer type (DAT)", "Dementia of the Alzheimer's type NOS", "Dementia, Primary Senile Degenerative", "senile dementia of the Alzheimer type", "SENILE DEMENTIA OF THE ALZHEIMER TYPE", "senile dementia of the Alzheimer type (SDAT)", "Late-onset form of familial Alzheimer disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alzheimer disease", "shortest_name_length": 2}
{"curie": "MONDO:0700148", "names": ["canine transitional cell carcinoma", "Canine Transitional Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canine transitional cell carcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0015213", "names": ["isolated visceral malformation", "nonsyndromic visceral malformation", "non-syndromic visceral malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-syndromic visceral malformation", "shortest_name_length": 30}
{"curie": "MONDO:0006583", "names": ["Necrobiosis Lipoidica", "necrobiosis lipoidica", "Necrobiosis lipoidica", "Lipoidica necrobiosis", "necrobiosis; lipoidica", "lipoidica; necrobiosis", "Oppenheim-Urbach disease", "lipoidica necrobiosis nld", "Necrobiosis lipoidica, NOS", "NLD - Necrobiosis lipoidica", "Necrobiosis lipoidica (disorder)", "necrobiosis lipoidica (diagnosis)", "necrobiosis lipoidica diabeticorum (formerly)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "necrobiosis lipoidica", "shortest_name_length": 21}
{"curie": "MONDO:0020433", "names": ["ectasia of the left auricle", "ectasia of the left appendage", "dilatation of the left auricle", "dilatation of the left appendage", "ectasia of the left atrial appendage", "dilatation of the left atrial appendage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectasia of the left appendage", "shortest_name_length": 27}
{"curie": "UMLS:C1458142", "names": ["squamous odontogenic tumor", "Squamous odontogenic tumor", "Squamous Odontogenic Tumor", "squamous odontogenic tumour", "Odontogenic Tumor, Squamous", "Squamous odontogenic tumour", "Squamous Odontogenic Tumors", "Tumor, Squamous Odontogenic", "Tumors, Squamous Odontogenic", "Odontogenic Tumors, Squamous", "Squamous Odontogenic Neoplasm", "Squamous odontogenic tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Squamous odontogenic tumor", "shortest_name_length": 26}
{"curie": "MONDO:0014126", "names": ["PRLTS4", "Perrault syndrome 4", "PERRAULT SYNDROME 4", "LARS2 Perrault syndrome", "Perrault syndrome type 4", "Perrault syndrome caused by mutation in LARS2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perrault syndrome 4", "shortest_name_length": 6}
{"curie": "MONDO:0014167", "names": ["FAME5", "FCMTE5", "familial adult myoclonic epilepsy 5", "EPILEPSY, FAMILIAL ADULT MYOCLONIC, 5", "epilepsy, familial adult myoclonic, 5", "epilepsy, familial ADULT myoclonic, 5", "epilepsy, myoclonic, familial adult, 5", "CNTN2 epilepsy, familial adult myoclonic", "epilepsy, familial adult myoclonic, type 5", "familial cortical myoclonic tremor and epilepsy 5", "cortical myoclonic tremor with epilepsy, familial, 5", "CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 5", "epilepsy, familial adult myoclonic caused by mutation in CNTN2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, familial adult myoclonic, 5", "shortest_name_length": 5}
{"curie": "UMLS:C4331406", "names": ["Third Ventricle Ependymal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Third Ventricle Ependymal Tumor", "shortest_name_length": 31}
{"curie": "MONDO:0002252", "names": ["HEPATITIS GRANULOMATOUS", "Hepatitis granulomatous", "hepatitis granulomatous", "granulomatous hepatitis", "Granulomatous hepatitis", "Granulomatous Hepatitis", "granulomatous; hepatitis", "hepatitis; granulomatous", "Hepatitis granulomatous NOS", "Granulomatous hepatitis (disorder)", "granulomatous hepatitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "granulomatous hepatitis", "shortest_name_length": 23}
{"curie": "MONDO:0007473", "names": ["DUS", "DRS", "DURS", "Duane", "Duane Anomaly", "DUANE ANOMALY", "Duane anomaly", "Duane syndrome", "DUANE SYNDROME", "duane syndrome", "Duane Syndrome", "Anomaly, Duane", "duanes syndrome", "Syndrome, Duane", "Duanes Syndrome", "duane's syndrome", "Duane's syndrome", "DUANE'S SYNDROME", "Duane's Syndrome", "duanes's syndrome", "Syndrome, Duane's", "retraction syndrome", "Retraction syndrome", "Retraction Syndrome", "RETRACTION SYNDROME", "Retraction Syndromes", "retraction; syndrome", "syndrome; retraction", "Isolated Duane Anomaly", "Eye retraction syndrome", "Duane Anomaly, Isolated", "Anomaly, Isolated Duane", "syndrome; eye retraction", "eye retraction; syndrome", "Isolated Duane Anomalies", "duane retraction syndrome", "Duane Anomalies, Isolated", "Duane retraction syndrome", "Duane Retraction Syndrome", "Duane syndrome retraction", "Ocular Retraction Syndrome", "Syndrome, Duane Retraction", "Retraction Syndrome, Duane", "duanes retraction syndrome", "Duane's retraction syndrome", "Ocular Retraction Syndromes", "Syndrome, Ocular Retraction", "duane's retraction syndrome", "Duane's syndrome (disorder)", "Retraction Syndrome, Ocular", "Stilling-Turk-Duane syndrome", "Stilling-Turk-Duane Syndrome", "Stilling Turk Duane Syndrome", "Duane's syndrome (diagnosis)", "Stilling-Turk-Duane Syndromes", "Co-Contractive Retraction Syndrome", "Isolated Duane Retraction Syndrome", "Co Contractive Retraction Syndrome", "Retraction Syndrome, Co-Contractive", "Co-Contractive Retraction Syndromes", "Limited eye movement from Duane anomaly", "Limited eye motility from Duane anomaly", "Globe retraction and deviation on adduction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Duane retraction syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C0854114", "names": ["Corneal epithelium defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Corneal epithelium defect", "shortest_name_length": 25}
{"curie": "UMLS:C4288141", "names": ["TERT Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "TERT Deficiency", "shortest_name_length": 15}
{"curie": "MONDO:0035663", "names": ["NMOSD with anti-AQP4 antibodies", "neuromyelitis optica spectrum disorder with anti-AQP4 antibodies", "Neuromyelitis optica spectrum disorder with anti-aquaporin 4 antibodies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuromyelitis optica spectrum disorder with anti-AQP4 antibodies", "shortest_name_length": 31}
{"curie": "UMLS:C0160354", "names": ["Duodenum injury with open wound into cavity", "Injury to duodenum with open wound into cavity", "injury of duodenum with open wound into cavity", "Injury to Duodenum with Open Wound into Cavity", "Injury to duodenum, with open wound into cavity", "Injury of duodenum with open wound into abdominal cavity", "injury of duodenum with open wound into cavity (diagnosis)", "Injury of duodenum with open wound into abdominal cavity (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of duodenum with open wound into abdominal cavity", "shortest_name_length": 43}
{"curie": "UMLS:C3272769", "names": ["Appendix EC Cell Serotonin-Producing NET", "Appendix EC Cell Serotonin-Producing Carcinoid Tumor", "Appendix EC-Cell Serotonin-Producing Neuroendocrine Tumor", "Appendix Enterochromaffin Cell Serotonin-Producing Carcinoid Tumor", "Appendix Enterochromaffin Cell Serotonin-Producing Neuroendocrine Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Appendix Enterochromaffin Cell Serotonin-Producing Neuroendocrine Tumor", "shortest_name_length": 40}
{"curie": "MONDO:0100306", "names": ["disorder of defective peroxisome oxidative status"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of defective peroxisome oxidative status", "shortest_name_length": 49}
{"curie": "OMIM:223380", "names": ["DOPAMINE BETA-HYDROXYLASE, PLASMA, THERMOLABILITY OF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 52}
{"curie": "UMLS:C1332225", "names": ["aggressive lymphoma", "NHL, aggressive, NOS", "Aggressive Non-Hodgkin Lymphoma", "Aggressive Non-Hodgkin's Lymphoma", "Non-Hodgkin lymphoma, aggressive, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aggressive Non-Hodgkin Lymphoma", "shortest_name_length": 19}
{"curie": "UMLS:C0151737", "names": ["Intentional injury", "intentional injury", "INTENTIONAL INJURY", "injuries intentional"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intentional injury", "shortest_name_length": 18}
{"curie": "UMLS:C4053892", "names": ["Ureteral Kinking"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ureteral Kinking", "shortest_name_length": 16}
{"curie": "UMLS:C0742545", "names": ["colon abscess", "COLON ABSCESS", "abscess colon", "colon; abscess", "abscess; colon", "Colonic abscess", "Infection causing abscess of colon", "infection of colon causing abscess", "Infection causing abscess of colon (disorder)", "Infection causing abscess of colon (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infection causing abscess of colon", "shortest_name_length": 13}
{"curie": "UMLS:C2825158", "names": ["Chronic Kidney Disease, Stage 0"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic Kidney Disease, Stage 0", "shortest_name_length": 31}
{"curie": "UMLS:C0686031", "names": ["Metastasis to the Oropharynx", "Metastatic Tumor to the Oropharynx", "Metastatic Neoplasm to the Oropharynx", "Secondary malignant neoplasm of oropharynx", "oropharyngeal neoplasm malignant secondary", "Metastatic malignant neoplasm of oropharynx", "Metastatic malignant neoplasm to oropharynx", "Metastatic Malignant Neoplasm in the Oropharynx", "Secondary malignant neoplasm of oropharynx, NOS", "Metastatic Malignant Neoplasm to the Oropharynx", "Metastatic malignant neoplasm to oropharynx, NOS", "Secondary malignant neoplasm of oropharynx (diagnosis)", "Metastatic malignant neoplasm to oropharynx (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to oropharynx", "shortest_name_length": 28}
{"curie": "UMLS:C0392050", "names": ["Laryngeal keratosis", "Laryngeal Keratosis", "leukoplakia; larynx", "larynx; leukoplakia", "Keratosis of Larynx", "leukoplakia of larynx", "Laryngeal leukoplakia", "Leukoplakia of larynx", "Laryngeal Leukoplakia", "Leucoplakia of larynx", "Laryngeal leucoplakia", "Keratosis of the Larynx", "Leukoplakia of larynx (disorder)", "Laryngeal squamous cell hyperplasia", "leukoplakia of larynx (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leukoplakia of larynx", "shortest_name_length": 19}
{"curie": "UMLS:C2983722", "names": ["Pharyngeal Carcinoma by AJCC v6 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pharyngeal Carcinoma by AJCC v6 Stage", "shortest_name_length": 37}
{"curie": "MONDO:0003567", "names": ["bilateral hypoactive labyrinth", "Bilateral hypoactive labyrinth", "hypoactive labyrinth, bilateral", "Hypoactive labyrinth, bilateral", "bilateral hypoactive labyrinth (diagnosis)", "hypoactive bilateral labyrinthine dysfunction", "Hypoactive bilateral labyrinthine dysfunction", "Hypoactive bilateral labyrinthine dysfunction (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bilateral hypoactive labyrinth", "shortest_name_length": 30}
{"curie": "MONDO:0043206", "names": ["Retained hair", "trichostasis spinulosa", "Trichostasis spinulosa", "Trichostasis spinulosa (disorder)", "elevated dark spiny papules on the face or trunk"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichostasis spinulosa", "shortest_name_length": 13}
{"curie": "UMLS:C2981275", "names": ["Stage IVC Thyroid Gland Medullary Cancer", "Stage IVC Thyroid Gland Medullary Carcinoma", "Stage IVC Thyroid Gland Medullary Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Thyroid Gland Medullary Carcinoma AJCC v7", "shortest_name_length": 40}
{"curie": "MONDO:0020174", "names": ["skin of eyelid precancerous condition", "precancerous lesion of palpebral epidermis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "precancerous lesion of palpebral epidermis", "shortest_name_length": 37}
{"curie": "MONDO:0024863", "names": ["Small Size Posterior Uveal Melanoma", "small size posterior uveal melanoma", "posterior uveal melanoma, small size", "melanoma, posterior uveal, small size", "uveal melanoma, posterior, small size", "Small Size Ciliary Body and Choroid Melanoma", "small size ciliary body and choroid melanoma", "ciliary body and choroid melanoma, small size", "intraocular melanoma ciliary body and choroid, small size", "melanoma, intraocular ciliary body and choroid small size"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small size posterior uveal melanoma", "shortest_name_length": 35}
{"curie": "UMLS:C4525657", "names": ["Stage II Jejunal Neuroendocrine Tumor", "Stage II Jejunal Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Jejunal Neuroendocrine Tumor AJCC v8", "shortest_name_length": 37}
{"curie": "MONDO:0015293", "names": ["SOLAMEN syndrome", "segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome", "Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome", "Segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus syndrome", "Segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal naevus syndrome", "Segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0003761", "names": ["Meningeal Melanoma", "Meningeal melanoma", "meningeal melanoma", "leptomeninx melanoma", "Leptomeningeal Melanoma", "leptomeningeal melanoma", "Melanoma of Leptomeninges", "melanoma of leptomeninges", "Melanoma of the Leptomeninges", "melanoma of the leptomeninges", "malignant melanoma of meninges", "leptomeninx melanoma (disease)", "melanoma (disease) of leptomeninx", "Meningeal melanoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leptomeningeal melanoma", "shortest_name_length": 18}
{"curie": "UMLS:C5420782", "names": ["Conjunctival Blue Nevus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conjunctival Blue Nevus", "shortest_name_length": 23}
{"curie": "UMLS:C1334375", "names": ["Larynx Paraganglioma", "Laryngeal Paraganglioma", "Paraganglioma of Larynx", "Paraganglioma of the Larynx"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laryngeal Paraganglioma", "shortest_name_length": 20}
{"curie": "UMLS:C0752161", "names": ["Extracerebral Cavernous Hemangioma", "Cavernous Hemangioma, Extracerebral", "Hemangioma, Extracerebral Cavernous", "Extracerebral Cavernous Hemangiomas", "Cavernous Hemangiomas, Extracerebral", "Hemangiomas, Extracerebral Cavernous"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cavernous Hemangioma, Extracerebral", "shortest_name_length": 34}
{"curie": "UMLS:C0948816", "names": ["Catheter site hematoma", "Catheter site haematoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Catheter site hematoma", "shortest_name_length": 22}
{"curie": "UMLS:C3273008", "names": ["H-HCA", "HNF1alpha-Inactivated Hepatocellular Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HNF1alpha-Inactivated Hepatocellular Adenoma", "shortest_name_length": 5}
{"curie": "UMLS:C4763425", "names": ["Unresectable Paraganglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Paraganglioma", "shortest_name_length": 26}
{"curie": "MONDO:0019118", "names": ["fundus dystrophy", "dystrophy; retina", "retinal dystrophy", "retina; dystrophy", "Retinal dystrophy", "Retinal Dystrophy", "Dystrophy, Retinal", "dystrophies retinal", "Retinal Dystrophies", "Dystrophies, Retinal", "genetic retinal dystrophy", "familial retinal dystrophy", "Inherited retinal disorder", "inherited retinal dystrophy", "hereditary retinal dystrophy", "Hereditary retinal dystrophy", "Retinal dystrophy (disorder)", "Hereditary Retinal Dystrophy", "Hereditary retinal dystrophies", "hereditary retinal degeneration", "Hereditary retinal dystrophy, NOS", "Hereditary retinal dystrophy (disorder)", "hereditary retinal dystrophy (diagnosis)", "Unspecified hereditary retinal dystrophy", "Hereditary retinal dystrophy, unspecified", "Breakdown of light-sensitive cells in back of eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited retinal dystrophy", "shortest_name_length": 16}
{"curie": "UMLS:C0279541", "names": ["Adult NSHD", "NSHD, adult", "NS HD, adult", "nodular sclerosing HD, adult", "HD, nodular sclerosis, adult", "Adult Hodgkin's Nodular Sclerosis", "adult nodular sclerosis Hodgkin lymphoma", "Adult Nodular Sclerosis Hodgkin Lymphoma", "Adult Nodular Sclerosis Hodgkin's Disease", "adult nodular sclerosis Hodgkin's disease", "Adult Nodular Sclerosis Hodgkin's Lymphoma", "nodular sclerosis Hodgkin's disease, adult", "adult Hodgkin's disease, nodular sclerosis", "nodular sclerosing Hodgkin's disease, adult", "Hodgkin's disease, nodular sclerosis, adult", "lymphoma, nodular sclerosing adult Hodgkin's", "Nodular Sclerosis Classical Hodgkin Lymphoma", "Hodgkin's lymphoma, nodular sclerosis, adult", "Adult Nodular Sclerosis Classic Hodgkin Lymphoma", "Adult Nodular Sclerosis Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Nodular Sclerosis Classical Hodgkin Lymphoma", "shortest_name_length": 10}
{"curie": "MONDO:0008959", "names": ["CHANDS", "CHAND syndrome", "CHAND SYNDROME", "Baughman syndrome", "curly hair-ankyloblepharon-nail dysplasia syndrome", "Curly hair-ankyloblepharon-nail dysplasia syndrome", "CURLY HAIR-ANKYLOBLEPHARON-NAIL DYSPLASIA SYNDROME", "Curly hair, ankyloblepharon, nail dysplasia syndrome", "CHANDS - Curly hair, ankyloblepharon, nail dysplasia syndrome", "Curly hair, ankyloblepharon, nail dysplasia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CHAND syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0011619", "names": ["Crumpled helices and small mouth", "crumpled helices and small mouth", "CRUMPLED HELICES AND SMALL MOUTH", "Sparse hair, prominent nose, small mouth, micrognathia, cleft palate, crumpled upper helices, digit anomaly, and mild developmental delay", "sparse hair, prominent nose, small mouth, micrognathia, cleft palate, crumpled upper helices, digit anomaly, and mild developmental delay"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "crumpled helices and small mouth", "shortest_name_length": 32}
{"curie": "MONDO:0012105", "names": ["Wg", "GPA", "Wegener", "WG, FORMERLY", "Klinger's disease", "wegener's syndrome", "Wegener's syndrome", "Wegener Granulomatosis", "Midline granulomatosis", "Wegener granulomatosis", "wegener granulomatosis", "WEGENER GRANULOMATOSIS", "granulomatosis wegener", "Wegener; granulomatosis", "wegeners granulomatosis", "Wegeners granulomatosis", "WEGENERS GRANULOMATOSIS", "Granulomatosis, Wegener", "GRANULOMATOSIS, WEGENER", "granulomatosis; Wegener", "granulomatosis wegeners", "Wegener's Granulomatosis", "wegener's granulomatosis", "granulomatosis wegener's", "Wegener's granulomatosis", "WEGENER'S GRANULOMATOSIS", "Granulomatosis, Wegener's", "granulomatosis - Wegener's", "Granulomatous polyangiitis", "ANCA-associated vasculitis", "necrotizing; granulomatosis", "granulomatosis; necrotizing", "Wegener's granulomatosis NOS", "GRANULOMATOSIS WITH POLYANGIITIS", "Granulomatosis with polyangiitis", "Wegener granulomatosis, formerly", "granulomatosis with polyangiitis", "WEGENER GRANULOMATOSIS, FORMERLY", "Granulomatosis with Polyangiitis", "with Polyangiitis, Granulomatosis", "Polyangiitis, Granulomatosis with", "Granulomatosis with Polyangiitides", "Polyangiitides, Granulomatosis with", "with Polyangiitides, Granulomatosis", "necrotizing respiratory granulomatosis", "Necrotizing respiratory granulomatosis", "Necrotising respiratory granulomatosis", "GRANULOMATOSIS, NECROTIZING RESPIRATORY", "Granulomatosis with polyangiitis (disorder)", "Granulomatosis with polyangiitis (diagnosis)", "Pauci-immune Glomerulonephritis associated with Granulomatosis with Polyangiitis", "pauci-immune glomerulonephritis associated with granulomatosis with polyangiitis", "Pauci-Immune Glomerulonephritis associated with Granulomatosis with Polyangiitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "granulomatosis with polyangiitis", "shortest_name_length": 2}
{"curie": "UMLS:C1336213", "names": ["Stage IIIA Ovarian Germ Cell Tumor", "Stage IIIA Ovarian Germ Cell Tumor AJCC v7", "Stage IIIA Ovarian Germ Cell Tumor AJCC v6", "Stage IIIA Ovarian Germ Cell Tumor AJCC v6 and v7", "FIGO Stage IIIA Malignant Ovarian Germ Cell Tumor", "FIGO Stage IIIA Malignant Germ Cell Tumor of Ovary", "FIGO Stage IIIA Malignant Ovarian Germ Cell Neoplasm", "FIGO Stage IIIA Malignant Germ Cell Neoplasm of Ovary", "FIGO Stage IIIA Malignant Germ Cell Tumor of the Ovary", "FIGO Stage IIIA Malignant Germ Cell Neoplasm of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Ovarian Germ Cell Tumor AJCC v6 and v7", "shortest_name_length": 34}
{"curie": "UMLS:C0234484", "names": ["Syntactic disorder", "Syntactical aphasia", "Syntactical Aphasia", "Syntactical Aphasias", "Aphasia, Syntactical", "Aphasia, syntactical", "Syntactic impairment", "Syntactic difficulties", "Syntactical aphasia (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aphasia, Syntactical", "shortest_name_length": 18}
{"curie": "UMLS:C1541567", "names": ["Oligodendroglial Tumor", "Adult Oligodendroglial Tumor", "adult oligodendroglial tumors", "Brain tumor, adult: Oligodendroglioma/Oligodendroglial tumors"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Oligodendroglial Tumor", "shortest_name_length": 22}
{"curie": "MONDO:0002240", "names": ["Acute perichondritis of pinna", "acute perichondritis of pinna", "acute perichondritis of auricle", "perichondritis of auricle, acute", "Acute perichondritis of pinna (disorder)", "acute perichondritis of auricle (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute perichondritis of pinna", "shortest_name_length": 29}
{"curie": "UMLS:C0279076", "names": ["adult intermediate grade NHL", "adult NHL, intermediate grade", "NHL, adult intermediate grade", "Intermediate Grade Adult Non-Hodgkin's Lymphoma", "intermediate grade adult non-Hodgkin's lymphoma", "lymphoma, adult intermediate grade non-Hodgkin's", "non-Hodgkin's lymphoma, adult intermediate grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intermediate Grade Adult Non-Hodgkin's Lymphoma", "shortest_name_length": 28}
{"curie": "MONDO:0009447", "names": ["ichthyosis, split hairs, and amino aciduria", "ICHTHYOSIS, SPLIT HAIRS, AND AMINO ACIDURIA", "Ichthyosis, Split Hairs, and Amino Aciduria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ichthyosis, split hairs, and amino aciduria", "shortest_name_length": 43}
{"curie": "MONDO:0020662", "names": ["Borderline Ovarian Serous Tumor", "borderline ovarian serous tumor", "Borderline Serous Tumor of Ovary", "Borderline serous tumor of ovary", "borderline serous tumor of ovary", "Borderline serous tumour of ovary", "borderline ovarian serous neoplasm", "proliferating ovarian serous tumor", "Proliferating Ovarian Serous Tumor", "Borderline Ovarian Serous Neoplasm", "borderline serous neoplasm of ovary", "Borderline Serous Neoplasm of Ovary", "proliferating serous tumor of ovary", "Proliferating Serous Tumor of Ovary", "borderline serous tumor of the ovary", "Borderline Serous Tumor of the Ovary", "Proliferating Ovarian Serous Neoplasm", "proliferating ovarian serous neoplasm", "proliferating serous neoplasm of ovary", "Proliferating Serous Neoplasm of Ovary", "borderline serous neoplasm of the ovary", "Borderline Serous Neoplasm of the Ovary", "Proliferating Serous Tumor of the Ovary", "proliferating serous tumor of the ovary", "proliferating serous neoplasm of the ovary", "Proliferating Serous Neoplasm of the Ovary", "Ovarian Serous Tumor of Low Malignant Potential", "serous ovarian tumor of low malignant potential", "Serous Ovarian Tumor of Low Malignant Potential", "ovarian serous tumor of low malignant potential", "Serous Ovarian Neoplasm of Low Malignant Potential", "Ovarian Serous Neoplasm of Low Malignant Potential", "serous tumor of ovary with low malignant potential", "Serous Tumor of Ovary with Low Malignant Potential", "ovarian serous neoplasm of low malignant potential", "serous ovarian neoplasm of low malignant potential", "serous neoplasm of ovary with low malignant potential", "Serous Neoplasm of Ovary with Low Malignant Potential", "Serous Tumor of the Ovary with Low Malignant Potential", "serous tumor of the ovary with low malignant potential", "ovarian serous cystadenoma with proliferating activity", "cystadenoma with proliferating activity, ovarian serous", "cystadenoma with proliferating activity, serous, ovarian", "serous neoplasm of the ovary with low malignant potential", "Serous Neoplasm of the Ovary with Low Malignant Potential", "serous cystadenoma with proliferating activity, of the ovary", "ovary cancer, serous cystadenoma with proliferating activity", "ovarian cancer, serous cystadenoma with proliferating activity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "borderline ovarian serous tumor", "shortest_name_length": 31}
{"curie": "MONDO:0016173", "names": ["non-paraneoplastic sensory neuronopathy", "non-paraneoplastic sensory ganglionopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-paraneoplastic sensory ganglionopathy", "shortest_name_length": 39}
{"curie": "UMLS:C0008686", "names": ["Chronic glomerulonephritis with lesion of membranous glomerulonephritis", "Chronic Glomerulonephritis with Lesion of Membranous Glomerulonephritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic glomerulonephritis with lesion of membranous glomerulonephritis", "shortest_name_length": 71}
{"curie": "UMLS:C3697010", "names": ["Ulcerative colitis in remission", "Ulcerative colitis in remission (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ulcerative colitis in remission", "shortest_name_length": 31}
{"curie": "UMLS:C3640086", "names": ["CAVC-tetralogy of Fallot", "Complete AVSD-tetralogy of Fallot", "Tetralogy of Fallot - Complete AV Canal Defect", "Complete atrioventricular canal defect-tetralogy of Fallot", "Complete atrioventricular septal defect-tetralogy of Fallot", "Complete Atrioventricular Septal Defect with Tetralogy of Fallot"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Complete Atrioventricular Septal Defect with Tetralogy of Fallot", "shortest_name_length": 24}
{"curie": "MONDO:0012572", "names": ["Sakoda complex", "Sakoda Complex", "SAKODA COMPLEX", "Sakoda Spectrum", "Sakoda spectrum", "SAKODA SPECTRUM", "sphenoethmoidal encephalomeningocele agenesis of the corpus callosum and cleft lip/palate", "Sphenoethmoidal Encephalomeningocele, Agenesis of the Corpus Callosum, and Cleft Lip-Palate", "sphenoethmoidal encephalomeningocele, agenesis of the corpus callosum, and cleft Lip/palate", "SPHENOETHMOIDAL ENCEPHALOMENINGOCELE, AGENESIS OF THE CORPUS CALLOSUM, AND CLEFT LIP/PALATE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sakoda complex", "shortest_name_length": 14}
{"curie": "MONDO:0016586", "names": ["SM", "MASTSYS", "Mast cell disease", "Systemic mastocytosis", "Systemic Mastocytosis", "mastocytosis systemic", "systemic mastocytosis", "Systemic Mastocytoses", "malignant mastocytosis", "Mastocytoses, Systemic", "Malignant mastocytosis", "Malignant Mastocytosis", "Mastocytosis, Systemic", "MASTOCYTOSIS, SYSTEMIC", "mastocytosis; malignant", "malignant; mastocytosis", "[M]Malignant mastocytosis", "systemic mast-cell disease", "Systemic Mast-Cell Disease", "Systemic mast cell disease", "Systemic mastocytosis, NOS", "systemic mast cell disease", "MAST CELL TUMOR, MALIGNANT", "Systemic Mast Cell Disease", "systemic; mast cell disease", "Mast-Cell Disease, Systemic", "MAST CELL DISEASE, SYSTEMIC", "Systemic Mast-Cell Diseases", "Mast-Cell Diseases, Systemic", "systemic urticaria pigmentosa", "Urticaria pigmentosa, systemic", "Agressive systemic mastocytosis", "systemic mastocytosis (diagnosis)", "systemic tissue mast cell disease", "SMCD - systemic mast cell disease", "Systemic tissue mast cell disease", "systemic tissue Mast cell disease", "Systemic Tissue Mast Cell Disease", "Malignant mastocytosis (disorder)", "malignant mastocytosis (diagnosis)", "Systemic mast cell disease (disorder)", "Malignant systemic tissue mast cell disease", "Malignant mastocytosis (morphologic abnormality)", "disease (or disorder); systemic tissue, mast cell", "malignant mastocytosis of reticuloendothelial system", "malignant mastocytosis of reticuloendothelial system (diagnosis)", "systemic mastocytosis with associated hemotologic non-mast cell lineage disease (SM-AHNMD)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "systemic mastocytosis", "shortest_name_length": 2}
{"curie": "UMLS:C0267055", "names": ["esophagitis erosive", "erosive esophagitis", "ESOPHAGITIS EROSIVE", "Erosive esophagitis", "Erosive oesophagitis", "erosive oesophagitis", "Erosive esophagitis (disorder)", "Erosive esophagitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Erosive esophagitis", "shortest_name_length": 19}
{"curie": "UMLS:C0685024", "names": ["Benign Hilar Lung Tumor", "Benign Lung Hilum Tumor", "Benign Lung Hilum Neoplasm", "Benign Hilar Lung Neoplasm", "Benign neoplasm of hilus of lung", "Benign neoplasm of hilus of lung (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign neoplasm of hilus of lung", "shortest_name_length": 23}
{"curie": "MONDO:0012379", "names": ["ASRT3", "asthma-related traits, susceptibility to, 3", "ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 3", "asthma-related traits, susceptibility to, type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "asthma-related traits, susceptibility to, 3", "shortest_name_length": 5}
{"curie": "UMLS:C1516986", "names": ["Evaluable", "evaluable disease", "Evaluable Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Evaluable Disease", "shortest_name_length": 9}
{"curie": "MONDO:0007327", "names": ["hyperlipoproteinemia, type 1C", "HYPERLIPOPROTEINEMIA, TYPE IC", "Hyperlipoproteinemia, Type IC", "familial chylomicronemia due to inhibition of lipoprotein lipase activity", "CHYLOMICRONEMIA, FAMILIAL, DUE TO CIRCULATING INHIBITOR OF LIPOPROTEIN LIPASE", "Chylomicronemia, Familial, due to Circulating Inhibitor of Lipoprotein Lipase", "chylomicronemia, familial, due to circulating inhibitor of lipoprotein lipase"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chylomicronemia, familial, due to circulating inhibitor of lipoprotein lipase", "shortest_name_length": 29}
{"curie": "UMLS:C4528207", "names": ["Plasma Cell Myeloma by ISS Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Plasma Cell Myeloma by ISS Stage", "shortest_name_length": 32}
{"curie": "MONDO:0003643", "names": ["giant hemangioma", "Giant Hemangioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "giant hemangioma", "shortest_name_length": 16}
{"curie": "MONDO:0012341", "names": ["CELIAC3", "CTLA4 celiac disease", "susceptibility to celiac disease 3", "CELIAC DISEASE, SUSCEPTIBILITY TO, 3", "celiac disease, susceptibility to, 3", "celiac disease, susceptibility to, type 3", "celiac disease caused by mutation in CTLA4", "CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding)", "GLUTEN-SENSITIVE ENTEROPATHY, SUSCEPTIBILITY TO, 3", "gluten-sensitive enteropathy, susceptibility to, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "celiac disease, susceptibility to, 3", "shortest_name_length": 7}
{"curie": "UMLS:C0266798", "names": ["Cord compression", "cord compression", "Umbilical Cord Compression", "umbilical cord compression", "Umbilical cord compression", "Umbilical cord, compression", "Compression of umbilical cord", "umbilical cord compression (diagnosis)", "Compression of umbilical cord (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Compression of umbilical cord", "shortest_name_length": 16}
{"curie": "MONDO:0024650", "names": ["drug; osteoporosis", "drug induced osteoporosis", "drug-induced osteoporosis", "Drug-induced osteoporosis", "osteoporosis; drug-induced", "drugs induced osteoporosis", "Drug-induced osteoporosis (disorder)", "drug-induced osteoporosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "drug-induced osteoporosis", "shortest_name_length": 18}
{"curie": "MONDO:0018612", "names": ["cretin", "Cretinism", "cretinism", "CRETINISM", "Cretinism, NOS", "Congenital goiter", "congenital goiter", "Congenital goitre", "Goitrous cretinism", "CRETINISM, INFANTILE", "Endemic cretinism NOS", "infantile hypothyroidism", "cretin; type hypothyroid", "Infantile hypothyroidism", "HYPOTHYROIDISM CONGENITAL", "hypothyroidism congenital", "Congenital hypothyroidism", "HYPOTHYROIDISM, INFANTILE", "Congenital Hypothyroidism", "congenital hypothyroidism", "Hypothyroidism;congenital", "Hypothyroidism congenital", "hypothyroidism; congenital", "congenital; hypothyroidism", "hypothyroid; cretin (type)", "Hypothyroidism, congenital", "Hypothyroidism, Congenital", "HYPOTHYROIDISM, CONGENITAL", "Congenital hypothyroidism NOS", "CHT - Congenital hypothyroidism", "Fetal iodine deficiency syndrome", "fetal iodine deficiency syndrome", "Congenital thyroid insufficiency", "Foetal iodine deficiency syndrome", "insufficiency; thyroid, congenital", "thyroid; insufficiency, congenital", "Congenital hypothyroidism (disorder)", "Underactive thyroid gland from birth", "congenital hypothyroidism (diagnosis)", "Congenital iodine-deficiency syndrome", "congenital iodine deficiency syndrome", "Congenital iodine deficiency syndrome", "iodine-deficiency; syndrome, congenital", "iodine; deficiency, congenital syndrome", "deficiency; iodine, congenital syndrome", "hypothyroidism congenital with cretinism", "Congenital iodine deficiency hypothyroidism", "Congenital Iodine Deficiency Hypothyroidism", "iodine-deficiency; hypothyroidism, congenital", "hypothyroidism; iodine-deficiency, congenital", "Congenital iodine-deficiency hypothyroidism NOS", "Congenital iodine deficiency syndrome (disorder)", "Congenital iodine-deficiency syndrome (diagnosis)", "Congenital iodine-deficiency syndrome, unspecified", "congenital hypothyroidism not due to iodine deficiency", "Congenital hypothyroidism not due to iodine deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital hypothyroidism", "shortest_name_length": 6}
{"curie": "MONDO:0004415", "names": ["Lipid-rich urothelial carcinoma", "lipid-cell variant infiltrating bladder urothelial carcinoma", "Infiltrating Bladder Urothelial Carcinoma, Lipid-Cell Variant", "infiltrating bladder urothelial carcinoma, Lipid-cell variant", "Infiltrating Bladder Urothelial Carcinoma, Lipid-Rich Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lipid-cell variant infiltrating bladder urothelial carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0010846", "names": ["EXT3", "exostoses, multiple, type 3", "exostoses, multiple, type III", "Exostoses, Multiple, Type III", "EXOSTOSES, MULTIPLE, TYPE III", "EXOSTOSES, MULTIPLE, TYPE III (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exostoses, multiple, type III", "shortest_name_length": 4}
{"curie": "MONDO:0011980", "names": ["AITD1", "AUTOIMMUNE THYROID DISEASE, SUSCEPTIBILITY TO, 1", "autoimmune thyroid disease, susceptibility to, 1", "autoimmune thyroid disease, susceptibility to, type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune thyroid disease, susceptibility to, 1", "shortest_name_length": 5}
{"curie": "MONDO:0012463", "names": ["RP35", "RP 35", "retinitis pigmentosa 35", "Retinitis Pigmentosa 35", "RETINITIS PIGMENTOSA 35", "SEMA4A retinitis pigmentosa", "retinitis pigmentosa type 35", "retinitis pigmentosa caused by mutation in SEMA4A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 35", "shortest_name_length": 4}
{"curie": "UMLS:C0279965", "names": ["low-grade, stage II adult NHL", "NHL, low grade, stage II adult", "adult NHL, stage II, low grade", "Stage II Low Grade Adult Non-Hodgkin's Lymphoma", "non-Hodgkin's lymphoma, low grade, stage II adult", "lymphoma, low grade, stage II adult non-Hodgkin's", "adult non-Hodgkin's lymphoma, low grade, stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Low Grade Adult Non-Hodgkin's Lymphoma", "shortest_name_length": 29}
{"curie": "MONDO:0009884", "names": ["VIENNA-HIETZING DEFECT", "Vienna-Hietzing defect", "Vienna-Hietzing Defect", "platelet prostacyclin receptor defect", "Platelet Prostacyclin Receptor Defect", "PLATELET PROSTACYCLIN RECEPTOR DEFECT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "platelet prostacyclin receptor defect", "shortest_name_length": 22}
{"curie": "MONDO:0017360", "names": ["Mutase0 methylmalonic acidemia", "Mutase0 methylmalonic acidaemia", "complete deficiency of methylmalonyl-CoA mutase", "Complete deficiency of methylmalonyl-CoA mutase", "Complete deficiency of methylmalonyl-coenzyme A mutase", "Vitamin B12-unresponsive methylmalonic acidemia type mut0", "Vitamin B12-unresponsive methylmalonic aciduria type mut0", "vitamin B12-unresponsive methylmalonic acidemia type mut0", "vitamin B12-unresponsive methylmalonic aciduria type mut0", "Complete deficiency of methylmalonyl-coenzyme A mutase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitamin B12-unresponsive methylmalonic acidemia type mut0", "shortest_name_length": 30}
{"curie": "MONDO:0100226", "names": ["PSMNSW", "PSMNST", "LUNATISM", "sleepwalk", "sleep walk", "sleepwalked", "SOMNAMBULISM", "sleepwalking", "Sleepwalking", "somnambulism", "Somnambulism", "Somnanbulism", "somnanbulism", "Sleep Walking", "SLEEP WALKING", "Sleep walking", "sleep walking", "somnambulation", "Somnambulation", "sleeping walking", "Nocturnal Wandering", "Wandering, Nocturnal", "Disorder;sleepwalking", "Sleepwalking disorder", "sleepwalking disorder", "sleep walking disorder", "Sleep Walking Disorder", "sleepwalking (symptom)", "Sleep walking disorder", "Sleep Walking Disorders", "Sleepwalking [somnambulism]", "parasomnia, sleepwalking type", "PARASOMNIA, SLEEPWALKING TYPE", "parasomnia, sleep terrors type", "PARASOMNIA, SLEEP TERRORS TYPE", "sleepwalking disorder nonorganic", "nonorganic sleepwalking disorder", "Sleep walking disorder (disorder)", "nonorganic sleepwalking disorder (diagnosis)", "parasomnia, sleepwalking type, multifactorial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parasomnia, sleepwalking type", "shortest_name_length": 6}
{"curie": "MONDO:0001616", "names": ["Lobo", "Lacazioses", "Lacaziosis", "Lobomycoses", "Lobomycosis", "lobomycosis", "Lobo's disease", "Jorge Lobo Disease", "Disease, Jorge Lobo", "Jorge Lobos Disease", "Jorge Lobo's Disease", "keloid; blastomycotic", "Lobomycosis infection", "Disease, Jorge Lobo's", "cutaneous lobomycosis", "Cutaneous lobomycosis", "Keloidal Blastomycosis", "infection; Loboa loboi", "Keloidal blastomycosis", "Lobomycosis (disorder)", "Keloidal Blastomycoses", "Loboa loboi; infection", "Cutaneous blastomycosis", "Blastomycosis, Keloidal", "Blastomycosis, keloidal", "cutaneous blastomycosis", "Cheloidal blastomycosis", "blastomycosis; keloidal", "lobomycosis (diagnosis)", "Blastomycoses, Keloidal", "Lacazia loboi Infection", "infection by Loboa loboi", "Lacazia loboi Infections", "Infection, Lacazia loboi", "Infection by Loboa loboii", "Infections by Loboa loboi", "Infections by Blastomyces loboi", "blastomycotic infection lobomycosis", "Infection by Paracoccidioides loboii"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lobomycosis", "shortest_name_length": 4}
{"curie": "UMLS:C1333859", "names": ["Grade 2 Colon Adenocarcinoma", "Grade II Colon Adenocarcinoma", "Moderately Differentiated Colon Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade 2 Colon Adenocarcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0011641", "names": ["baculum, congenital absence of", "BACULUM, CONGENITAL ABSENCE OF", "OS PENIS, CONGENITAL ABSENCE OF", "Os penis, congenital absence of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "baculum, congenital absence of", "shortest_name_length": 30}
{"curie": "MONDO:0021494", "names": ["Benign Parotid Tumor", "benign parotid tumor", "Benign parotid tumor", "Benign parotid tumour", "Benign Tumor of Parotid", "benign tumor of parotid", "parotid neoplasm benign", "Benign Parotid Neoplasm", "benign parotid neoplasm", "Benign Parotid Gland Tumor", "benign parotid gland tumor", "benign neoplasm of parotid", "Benign Neoplasm of Parotid", "benign tumor of the parotid", "Benign Tumor of the Parotid", "benign tumor of parotid gland", "Benign Tumor of Parotid Gland", "benign parotid gland neoplasm", "parotid gland benign neoplasm", "Benign tumor of parotid gland", "Benign Parotid Gland Neoplasm", "benign neoplasm of the parotid", "Benign tumour of parotid gland", "Benign Neoplasm of the Parotid", "benign neoplasm of parotid gland", "Benign neoplasm of parotid gland", "Benign Neoplasm of Parotid Gland", "Benign Tumor of the Parotid Gland", "benign tumor of the parotid gland", "Benign Neoplasm of the Parotid Gland", "benign neoplasm of the parotid gland", "benign neoplasm of parotid (diagnosis)", "Benign neoplasm of parotid gland (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of parotid gland", "shortest_name_length": 20}
{"curie": "MONDO:0002412", "names": ["GSD", "Gierke", "Glycogenosis", "glycogenoses", "glycogenosis", "Glycogenoses", "Glycogenosis, NOS", "disease glycogen storage", "Glycogen Storage Disease", "glycogen storage disease", "Glycogen storage disease", "thesaurismosis; glycogen", "glycogen storage disorder", "storage disease; glycogen", "Storage Disease, Glycogen", "diseases glycogen storage", "Glycogen Storage Diseases", "glycogen storage diseases", "Glycogen storage disorder", "glycogen storage; disease", "Disease, Glycogen Storage", "Diseases, Glycogen Storage", "Storage Diseases, Glycogen", "disorders glycogen storage", "glycogen metabolism disorder", "Glycogen storage disorder NOS", "Glycogen storage disease, NOS", "GSD - Glycogen storage disease", "disorder of glycogen metabolism", "inborn glycogen storage disorder", "Glycogen storage disease (disorder)", "glycogen storage disease (diagnosis)", "Glycogen storage disease, unspecified", "inborn error of glycogen metabolic process", "inborn glycogen metabolic process disorder", "liver; disease, glycogen storage (etiology)", "rare inborn error of glycogen metabolic process", "liver; disease, glycogen storage (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of glycogen metabolism", "shortest_name_length": 3}
{"curie": "MONDO:0019068", "names": ["FMAIG", "Alloimmune neonatal renal disease", "alloimmune neonatal renal disease", "neonatal glomerulopathy due to neprilysin alloimmunization", "Neonatal glomerulopathy due to neprilysin alloimmunization", "neonatal glomerulopathy due to Neprilysin alloimmunization", "Fetomaternal alloimmunization with antenatal glomerulopathies", "fetomaternal alloimmunization with antenatal glomerulopathies", "Neonatal membranous glomerulopathy with maternal NEP deficiency", "neonatal membranous glomerulopathy with maternal NEP deficiency", "Neonatal membranous glomerulopathy with maternal neutral endopeptidase deficiency", "neonatal membranous glomerulopathy with maternal neutral endopeptidase deficiency", "congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization", "Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunisation", "Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization", "Congenital membranous nephropathy due to fetomaternal anti-neutral endopeptidase alloimmunization", "Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization (disorder)", "Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization", "shortest_name_length": 5}
{"curie": "MONDO:0033372", "names": ["DEE63", "EIEE63", "early infantile epileptic encephalopathy 63", "epileptic encephalopathy, early infantile, 63", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 63", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 63", "developmental and epileptic encephalopathy 63", "developmental and epileptic encephalopathy, 63"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 63", "shortest_name_length": 5}
{"curie": "UMLS:C1698484", "names": ["infection mucosa", "Mucosal Infection", "Mucosal infection", "Mucosal infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mucosal Infection", "shortest_name_length": 16}
{"curie": "MONDO:0012930", "names": ["SCN4", "Scn4", "Dursun syndrome", "Dursun Syndrome", "DURSUN SYNDROME", "SCN 4-Autosomal Recessive", "severe congenital neutropenia 4", "severe congenital neutropenia type 4", "Severe congenital neutropenia type 4", "Neutropenia, Severe Congenital, Autosomal Recessive 4", "neutropenia, severe congenital 4, autosomal recessive", "neutropenia, severe congenital, 4, autosomal recessive", "Neutropenia, Severe Congenital, 4, Autosomal Recessive", "NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE", "Severe Congenital Neutropenia Type 4, Autosomal Recessive", "Pulmonary Arterial Hypertension, Leukopenia, And Atrial Septal Defect", "PULMONARY ARTERIAL HYPERTENSION, LEUKOPENIA, AND ATRIAL SEPTAL DEFECT", "pulmonary arterial hypertension, leukopenia, and atrial septal defect", "autosomal recessive severe congenital neutropenia due to G6PC3 deficiency", "Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency", "severe congenital neutropenia-pulmonary hypertension-superficial venous angiectasis syndrome", "Severe congenital neutropenia-pulmonary hypertension-superficial venous angiectasis syndrome", "Severe congenital neutropenia, pulmonary hypertension, superficial venous angiectasis syndrome", "Autosomal recessive severe congenital neutropenia due to glucose-6-phosphatase catalytic subunit 3 deficiency", "Autosomal recessive severe congenital neutropenia due to glucose-6-phosphatase catalytic subunit 3 deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive severe congenital neutropenia due to G6PC3 deficiency", "shortest_name_length": 4}
{"curie": "UMLS:C5206757", "names": ["Refractory Childhood Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Childhood Malignant Neoplasm", "shortest_name_length": 39}
{"curie": "MONDO:0013504", "names": ["SPGF8", "NR5A1 azoospermia", "spermatogenic failure 8", "SPERMATOGENIC FAILURE 8", "spermatogenic failure type 8", "azoospermia caused by mutation in NR5A1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 8", "shortest_name_length": 5}
{"curie": "MONDO:0008898", "names": ["GCS1", "FTSS", "GCS 1", "FACIOTHORACOSKELETAL SYNDROME", "Faciothoracoskeletal Syndrome", "faciothoracoskeletal syndrome", "Facio-thoraco-skeletal syndrome", "Guadalajara camptodactyly syndrome", "Camptodactyly syndrome Guadalajara type 1", "camptodactyly syndrome Guadalajara type 1", "Guadalajara camptodactyly syndrome type 1", "Camptodactyly syndrome, Guadalajara type 1", "camptodactyly syndrome, Guadalajara type 1", "camptodactyly syndrome, Guadalajara, type 1", "CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I", "Camptodactyly Syndrome, Guadalajara, Type I", "camptodactyly syndrome, Guadalajara, type I", "Camptodactyly syndrome Guadalajara type 1 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "camptodactyly syndrome, Guadalajara type 1", "shortest_name_length": 4}
{"curie": "MONDO:0041447", "names": ["Metastatic Tumor to the Colon", "metastatic tumor to the colon", "Metastatic Neoplasm to the Colon", "metastatic neoplasm to the colon", "Secondary malignant neoplasm of colon", "secondary malignant neoplasm of colon", "Metastatic malignant neoplasm of colon", "Metastatic malignant neoplasm to colon", "Metastatic Malignant Neoplasm to the Colon", "metastatic malignant neoplasm in the colon", "Secondary malignant neoplasm of colon, NOS", "Metastatic Malignant Neoplasm in the Colon", "metastatic malignant neoplasm to the colon", "Metastatic malignant neoplasm to colon, NOS", "Metastatic malignant neoplasm to colon (disorder)", "secondary malignant neoplasm of colon (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metastatic malignant neoplasm in the colon", "shortest_name_length": 29}
{"curie": "UMLS:C0854797", "names": ["Resectable Hepatoblastoma", "Hepatoblastoma resectable", "Hepatoblastoma, Resectable"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatoblastoma resectable", "shortest_name_length": 25}
{"curie": "MONDO:0024314", "names": ["parasitemia", "Parasitemia", "Parasitemias"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parasitemia", "shortest_name_length": 11}
{"curie": "EFO:0003867", "names": ["rhabdomyolysis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rhabdomyolysis", "shortest_name_length": 14}
{"curie": "UMLS:C4684822", "names": ["Benign Lung PEComa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Lung PEComa", "shortest_name_length": 18}
{"curie": "MONDO:0013498", "names": ["SCZD15", "schizophrenia 15", "SCHIZOPHRENIA 15", "schizophrenia type 15", "schizophrenia 15 with or without an affective disorder", "SCHIZOPHRENIA 15 WITH OR WITHOUT AN AFFECTIVE DISORDER", "schizophrenia susceptibility locus, chromosome 22Q13-related", "SCHIZOPHRENIA SUSCEPTIBILITY LOCUS, CHROMOSOME 22q13-RELATED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schizophrenia 15", "shortest_name_length": 6}
{"curie": "MONDO:0012851", "names": ["NPHLOP2", "hypophosphatemic nephrolithiasis/osteoporosis 2", "nephrolithiasis/osteoporosis, hypophosphatemic, 2", "NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 2", "Nephrolithiasis-Osteoporosis, Hypophosphatemic, 2", "hypophosphatemic nephrolithiasis/osteoporosis type 2", "nephrolithiasis/osteoporosis, hypophosphatemic, type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypophosphatemic nephrolithiasis/osteoporosis 2", "shortest_name_length": 7}
{"curie": "UMLS:C0549384", "names": ["HHE", "hypotonic-hyporesponsive episode", "Hypotonic-hyporesponsive episode", "HYPOTONIC-HYPORESPONSIVE EPISODE", "Hypotonic-Hyporesponsive Episode", "episodes hypotonic hyporesponsive", "Hypotonic-hyporesponsive episode (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypotonic-hyporesponsive episode", "shortest_name_length": 3}
{"curie": "MONDO:0012654", "names": ["ASD4", "ATRIAL SEPTAL DEFECT 4", "Atrial Septal Defect 4", "atrial septal defect 4", "atrial septal defect type 4", "atrial heart septal defect 4", "atrial septal defect 4 - ASD4", "TBX20 atrial heart septal defect", "atrial heart septal defect type 4", "atrial septal defect 4 - ASD4 (diagnosis)", "atrial heart septal defect caused by mutation in TBX20"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial septal defect 4", "shortest_name_length": 4}
{"curie": "UMLS:C4329254", "names": ["Acquired Factor I Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired Factor I Deficiency", "shortest_name_length": 28}
{"curie": "MONDO:0021281", "names": ["retina cavernous angioma", "Retina Cavernous Angioma", "retinal cavernous angioma", "Retinal Cavernous Angioma", "Retinal cavernous angioma", "retina cavernous hemangioma", "Retina Cavernous Hemangioma", "cavernous angioma of retina", "Cavernous Angioma of Retina", "Retinal cavernous hemangioma", "retinal cavernous hemangioma", "Retinal Cavernous Hemangioma", "Retinal cavernous haemangioma", "cavernous hemangioma of retina", "Cavernous Hemangioma of Retina", "Cavernous hemangioma of retina", "Cavernous haemangioma of retina", "Cavernous Angioma of the Retina", "cavernous angioma of the retina", "Cavernous Hemangioma of the Retina", "cavernous hemangioma of the retina", "Cavernous hemangioma of retina (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cavernous hemangioma of retina", "shortest_name_length": 24}
{"curie": "UMLS:C4054752", "names": ["Hypocellular Myelodysplastic Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypocellular Myelodysplastic Syndrome", "shortest_name_length": 37}
{"curie": "MONDO:0008901", "names": ["TEL HASHOMER CAMPTODACTYLY SYNDROME", "Tel Hashomer camptodactyly syndrome", "Tel Hashomer camptodactyly syndrome (disorder)", "Camptodactyly-muscular hypoplasia-skeletal anomalies-abnormal palmar creases syndrome", "camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormal palmar creases", "CAMPTODACTYLY WITH MUSCULAR HYPOPLASIA, SKELETAL DYSPLASIA, AND ABNORMAL PALMAR CREASES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tel Hashomer camptodactyly syndrome", "shortest_name_length": 35}
{"curie": "MONDO:0003041", "names": ["Mesenchymal Chondrosarcoma", "mesenchymal chondrosarcoma", "pediatric mesenchymal chondrosarcoma", "Pediatric Mesenchymal Chondrosarcoma", "Childhood Mesenchymal Chondrosarcoma", "childhood mesenchymal chondrosarcoma", "mesenchymal chondrosarcoma of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pediatric mesenchymal chondrosarcoma", "shortest_name_length": 26}
{"curie": "MONDO:0000815", "names": ["fetal nicotine spectrum disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fetal nicotine spectrum disorder", "shortest_name_length": 32}
{"curie": "UMLS:C1333557", "names": ["FIGO Stage IIIC GTT", "FIGO Stage IIIC Gestational Trophoblastic Tumor", "FIGO Stage IIIC Gestational Trophoblastic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Stage IIIC Gestational Trophoblastic Tumor", "shortest_name_length": 19}
{"curie": "MONDO:0007248", "names": ["PPK nummularis", "callosities, painful plantar", "Callosities, Painful Plantar", "CALLOSITIES, PAINFUL PLANTAR", "hereditary painful callosities", "Hereditary painful callosities", "CALLOSITIES, HEREDITARY PAINFUL", "Callosities, Hereditary Painful", "callosities, hereditary painful", "Keratosis palmoplantaris nummularis", "keratosis palmoplantaris nummularis", "Plamoplantar keratoderma nummularis", "Plamoplantar hyperkeratosis nummularis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary painful callosities", "shortest_name_length": 14}
{"curie": "UMLS:C1337014", "names": ["ACT/CS1", "Atypical Cartilaginous Tumor/Grade I Chondrosarcoma", "Atypical Cartilaginous Tumor/Chondrosarcoma, Grade 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypical Cartilaginous Tumor/Chondrosarcoma, Grade 1", "shortest_name_length": 7}
{"curie": "UMLS:C0347020", "names": ["Metastasis to orbit", "Metastasis to the Orbit", "Secondary tumor of orbit", "Secondary tumour of orbit", "Metastatic Tumor to the Orbit", "Metastatic Neoplasm to the Orbit", "malignant orbital neoplasm secondary", "Secondary malignant neoplasm of orbit", "Metastatic malignant neoplasm to orbit", "Metastatic malignant neoplasm of orbit", "Metastatic Malignant Neoplasm in the Orbit", "Metastatic Malignant Neoplasm to the Orbit", "Secondary malignant neoplasm of orbit proper", "Secondary malignant neoplasm of orbit (diagnosis)", "Metastatic malignant neoplasm to orbit (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to orbit", "shortest_name_length": 19}
{"curie": "MONDO:0010480", "names": ["Class I G6PD deficiency", "FAVISM, SUSCEPTIBILITY TO", "hemolytic anemia due to G6PD deficiency", "severe hemolytic anemia due to G6PD deficiency", "class I glucose-6-phosphate dehydrogenase deficiency", "Anemia, Nonspherocytic Hemolytic, Due To G6pd Deficiency", "ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY", "anemia, nonspherocytic hemolytic, due to G6PD deficiency", "ANEMIA, NONSPEHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY", "hemolytic anemia, G6PD deficient (favism), X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anemia, nonspherocytic hemolytic, due to G6PD deficiency", "shortest_name_length": 23}
{"curie": "MONDO:0001444", "names": ["Chagas", "t cruzi", "t.cruzi", "chaga disease", "chagas disease", "chaga diseases", "CHAGAS DISEASE", "Chagas disease", "disease chagas", "Chagas Disease", "chagas diseases", "Chagas' disease", "Chagas' Disease", "chagas' disease", "Chagas-Mazza disease", "Chagas-mazza disease", "American Trypanosomiasis", "American trypanosomiasis", "Trypanosomiasis, American", "trypanosomiasis; American", "TRYPANOSOMIASIS, AMERICAN", "American; trypanosomiasis", "Chagas disease (diagnosis)", "TRYPANOSOMIASIS, BRAZILIAN", "cruzi infection trypanosoma", "Trypanosoma cruzi Infection", "Trypanosoma cruzi infection", "Trypanosoma cruzi Infections", "Infection, Trypanosoma cruzi", "American trypanosomiasis NOS", "infection; Trypanosoma cruzi", "Trypanosoma cruzi; infection", "Infections, Trypanosoma cruzi", "south American trypanosomiasis", "Chagas; disorder, other organs", "South American trypanosomiasis", "infection by trypanosoma cruzi", "Infection by Trypanosoma cruzi", "South American Trypanosomiasis", "Trypanosomiasis, South American", "Chagas; disorder, nervous system", "trypanosomiasis; Trypanosoma cruzi", "infection due to Trypanosoma cruzi", "Trypanosoma cruzi infectious disease", "disease (or disorder); organs, Chagas", "Trypanosoma cruzi disease or disorder", "infection caused by trypanosoma cruzi", "Infection caused by Trypanosoma cruzi", "Chagas disease with other organ involvement", "Trypanosoma cruzi caused disease or disorder", "chagas' disease with other organ involvement", "Chagas' disease with other organ involvement", "Chagas; disorder, digestive system (etiology)", "Chagas disease with nervous system involvement", "Chagas' disease with nervous system involvement", "chagas' disease with nervous system involvement", "Chagas disease with digestive system involvement", "Infection caused by Trypanosoma cruzi (disorder)", "chagas' disease with digestive system involvement", "Chagas' disease with digestive system involvement", "Chagas; disorder, digestive system (manifestation)", "Chagas' disease without mention of organ involvement", "Chagas disease with other organ involvement (diagnosis)", "Chagas' disease with other organ involvement (disorder)", "disease (or disorder); digestive system, Chagas (etiology)", "Chagas' disease with nervous system involvement (disorder)", "Chagas disease with nervous system involvement (diagnosis)", "Chagas disease with digestive system involvement (diagnosis)", "Chagas' disease with digestive system involvement (disorder)", "disease (or disorder); digestive system, Chagas (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chagas disease", "shortest_name_length": 6}
{"curie": "MONDO:0100506", "names": ["Cockayne spectrum with or without cerebrooculofacioskeletal syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cockayne spectrum with or without cerebrooculofacioskeletal syndrome", "shortest_name_length": 68}
{"curie": "UMLS:C0392622", "names": ["CCl4 Poisoning", "Poisoning, CCl4", "CCl4 Poisonings", "PERCHLOROMETHANE TOXICITY", "carbon tetrachloride poisoning", "CARBON TETRACHLORIDE POISONING", "Carbon tetrachloride poisoning", "Carbon Tetrachloride Poisoning", "Carbon Tetrachloride Poisonings", "Poisoning, Carbon Tetrachloride", "Poisonings, Carbon Tetrachloride", "Toxic effect of carbon tetrachloride", "Toxic effects of carbon tetrachloride", "poisoning solvents carbon tetrachloride", "poisoning by carbon tetrachloride vapors", "Toxic effects of carbon tetrachloride NOS", "Carbon tetrachloride causing toxic effect", "Toxic effect of carbon tetrachloride (disorder)", "poisoning solvents carbon tetrachloride (diagnosis)", "poisoning by carbon tetrachloride vapors (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Toxic effect of carbon tetrachloride", "shortest_name_length": 14}
{"curie": "UMLS:C5557161", "names": ["Stage IB2 Cervical Cancer AJCC v9", "Stage IB2 Cervical Carcinoma AJCC v9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB2 Cervical Cancer AJCC v9", "shortest_name_length": 33}
{"curie": "MONDO:0035136", "names": ["isolated melanotic schwannoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated melanotic schwannoma", "shortest_name_length": 29}
{"curie": "MONDO:0002322", "names": ["ANGIODYSPLASIA", "Angiodysplasia", "angiodysplasia", "angiodysplasias", "Angiodysplasias", "Angiodysplasia NOS", "colon angiodysplasia", "angiodysplasia colon", "colonic angiodysplasia", "Telangiectasia of colon", "ANGIODYSPLASIA OF COLON", "angiodysplasia of colon", "Angiodysplasia of colon", "Vascular ectasia of colon", "Large intestine angiodysplasia", "Angiodysplasia of large intestine", "Angiodysplasia of colon (disorder)", "colonic angiodysplasia (diagnosis)", "Vascular ectasia of colon (disorder)", "Angiodysplasia (morphologic abnormality)", "AV - Angiodysplasia malformation of colon", "angiodysplasia of stomach and duodenum with hemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angiodysplasia", "shortest_name_length": 14}
{"curie": "UMLS:C0262591", "names": ["pelvic adhesion", "Pelvic adhesions", "pelvic adhesions", "adhesions pelvic", "PELVIC ADHESIONS", "pelvic adhesions (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pelvic adhesions", "shortest_name_length": 15}
{"curie": "MONDO:0006764", "names": ["fungal meningitis", "Fungal Meningitis", "Meningitis fungal", "Fungal meningitis", "Meningitis, Fungal", "Fungal Meningitides", "Meningitides, Fungal", "Meningitis fungal NOS", "Meningitis in mycoses", "Fungal meningitis, NOS", "Fungi infectious meningitis", "Fungal meningitis (disorder)", "fungal meningitis (diagnosis)", "Fungi caused infectious meningitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fungal meningitis", "shortest_name_length": 17}
{"curie": "MONDO:0013371", "names": ["CMD1U", "dilated cardiomyopathy 1U", "CARDIOMYOPATHY, DILATED, 1U", "cardiomyopathy, dilated, 1U", "Cardiomyopathy, Dilated, 1u", "dilated cardiomyopathy type 1U", "cardiomyopathy, dilated, type 1U", "PSEN1 familial isolated dilated cardiomyopathy", "familial isolated dilated cardiomyopathy caused by mutation in PSEN1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1U", "shortest_name_length": 5}
{"curie": "MONDO:0016472", "names": ["GWD", "Medinensis", "medinensis", "guinea worm", "DRACONTIASIS", "Dracontiasis", "dracontiasis", "Dracunculosis", "Dracunculoses", "DRACUNCULIASIS", "dracunculiasis", "Dracunculiasis", "Dracunculiases", "Guinea worm disease", "Medina worm disease", "Guinea Worm Disease", "infestation; Medina", "Medina; infestation", "guinea worm disease", "Worm Disease, Guinea", "Guinea Worm Diseases", "Disease, Guinea Worm", "Diseases, Guinea Worm", "Guinea Worm Infection", "Guinea worm infection", "GUINEA WORM INFECTION", "Guinea-worm infection", "guinea worm infection", "Infection, Guinea Worm", "FIERY SERPENT INFECTION", "guinea worm; infestation", "infestation; guinea worm", "Dracontiasis - guinea-worm", "dracunculiasis (diagnosis)", "dracunculiasis (Guinea worm)", "infection by Dracunculus medinensis", "Infection by Dracunculus medinensis", "infection due to Dracunculus medinensis", "Dracunculus medinensis infectious disease", "Dracunculus medinensis disease or disorder", "Infection caused by Dracunculus medinensis", "Dracunculus medinensis caused disease or disorder", "parasitic infection caused by Dracunculus medinensis", "Infection caused by Dracunculus medinensis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dracunculiasis", "shortest_name_length": 3}
{"curie": "MONDO:0020119", "names": ["syndromic X-linked mental retardation", "mental retardation, X-linked syndromic", "syndromic X-linked intellectual disability", "X-linked syndromic intellectual disability", "intellectual disability, X-linked syndromic", "syndromic intellectual disability, X-linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked syndromic intellectual disability", "shortest_name_length": 37}
{"curie": "MONDO:0010916", "names": ["PKD3", "Pkd3", "Apkd3", "APKD3", "polycystic kidney disease 3", "polycystic kidney disease type 3", "polycystic kidney disease, type 3", "polycystic kidney disease, adult, type 3", "polycystic kidney disease, adult, type III", "POLYCYSTIC KIDNEY DISEASE, ADULT, TYPE III", "Polycystic Kidney Disease, Adult, Type III", "polycystic kidney disease 3, autosomal dominant", "GANAB autosomal dominant polycystic kidney disease", "POLYCYSTIC KIDNEY DISEASE 3 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE", "polycystic kidney disease 3 with or without polycystic liver disease", "autosomal dominant polycystic kidney disease caused by mutation in GANAB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polycystic kidney disease 3 with or without polycystic liver disease", "shortest_name_length": 4}
{"curie": "UMLS:C5400329", "names": ["Renal phospholipidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal phospholipidosis", "shortest_name_length": 22}
{"curie": "UMLS:C0043254", "names": ["wound penetrating", "penetrating wound", "Penetrating Wound", "Penetrating wound", "penetrating wounds", "Penetrating wounds", "penetrating injury", "Wound, penetrating", "penetrating; wound", "injury penetrating", "Wound, Penetrating", "Penetrating Wounds", "Penetrating injury", "Penetrating - wound", "Wounds, Penetrating", "injuries penetrating", "Penetrating wound (disorder)", "penetrating wound (physical finding)", "Penetrating wound (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wounds, Penetrating", "shortest_name_length": 17}
{"curie": "MONDO:0018429", "names": ["Del(14)(q24.1q24.3)", "monosomy 14q24.1q24.3", "14q24.1q24.3 microdeletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "14q24.1q24.3 microdeletion syndrome", "shortest_name_length": 19}
{"curie": "UMLS:C2861618", "names": ["acute monoblastic/monocytic leukemia in relapse", "Acute monoblastic/monocytic leukemia, in relapse", "Relapsed Acute Monoblastic and Monocytic Leukemia", "Recurrent Acute Monoblastic and Monocytic Leukemia", "acute monoblastic/monocytic leukemia in relapse (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute monoblastic/monocytic leukemia in relapse", "shortest_name_length": 47}
{"curie": "MONDO:0100392", "names": ["AML, t(11;17)", "acute myeloid leukemia, t(11;17)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, t(11;17)", "shortest_name_length": 13}
{"curie": "MONDO:0022177", "names": ["Trisomy 13q", "13q trisomy", "trisomy 13q", "13q syndrome", "13q+ syndrome", "Duplication 13q", "13q duplication", "dup(13q) syndrome", "partial trisomy 13q", "Chromosome 13q trisomy", "chromosome 13q trisomy", "13q duplication syndrome", "duplication 13q syndrome", "chromosome 13q duplication", "partial trisomy of chromosome 13q", "chromosome 13q duplication syndrome", "partial duplication of chromosome 13q", "partial trisomy of the long arm of chromosome 13", "partial duplication of the long arm of chromosome 13", "partial duplication of the long arm of chromosome type 13"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 13q trisomy", "shortest_name_length": 11}
{"curie": "MONDO:0012360", "names": ["RTSH", "CHNG3", "THYROTROPIN RESISTANCE", "thyrotropin resistance", "resistance to thyrotropin", "RESISTANCE TO THYROTROPIN", "congenital nongoitrous hypothyroidism 3", "congenital nongoitrous hypothryoidism 3", "Congenital Hypothyroidism, Nongoitrous, 3", "HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 3", "Hypothyroidism, Congenital, Nongoitrous, 3", "hypothyroidism, congenital, nongoitrous, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital nongoitrous hypothryoidism 3", "shortest_name_length": 4}
{"curie": "MONDO:0002702", "names": ["Cystadenocarcinoma ovary", "ovary cystadenocarcinoma", "ovarian cystadenocarcinoma", "Ovarian Cystadenocarcinoma", "Cystadenocarcinoma of Ovary", "cystadenocarcinoma of ovary", "Cystadenocarcinoma of ovary", "cystadenocarcinoma of the ovary", "cystadenocarcinoma of the Ovary", "Cystadenocarcinoma of the Ovary", "Cystadenocarcinoma of ovary (disorder)", "cystadenocarcinoma of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian cystadenocarcinoma", "shortest_name_length": 24}
{"curie": "MONDO:0019580", "names": ["Papular mucinosis of infancy", "papular mucinosis of infancy", "Cutaneous mucinosis of infancy", "cutaneous mucinosis of infancy", "Papular mucinosis of infancy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papular mucinosis of infancy", "shortest_name_length": 28}
{"curie": "UMLS:C4527336", "names": ["Recurrent Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type", "Recurrent Primary Cutaneous (Skin) Diffuse Large B-Cell Lymphoma, Leg Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type", "shortest_name_length": 67}
{"curie": "MONDO:0014807", "names": ["SMABF2", "spinal muscular atrophy with congenital bone fractures 2", "SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 2", "spinal muscular atrophy with congenital bone fractures type 2", "ASCC1 prenatal-onset spinal muscular atrophy with congenital bone fractures", "prenatal-onset spinal muscular atrophy with congenital bone fractures caused by mutation in ASCC1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal muscular atrophy with congenital bone fractures 2", "shortest_name_length": 6}
{"curie": "UMLS:C4527331", "names": ["Refractory Testicular Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Testicular Lymphoma", "shortest_name_length": 30}
{"curie": "UMLS:C0158026", "names": ["monarthritis", "gonarthritis", "Monarthritis", "MONARTHRITIS", "Gonarthritis", "Monoarthritis", "monoarthritis", "Monoarthritis, NOS", "ARTHRITIS SINGLE JOINT", "Arthritis single joint", "Monoarthritis (disorder)", "Unspecified monoarthritis", "monoarticular inflammation", "monoarticular inflammation (diagnosis)", "Unspecified monoarthritis, site unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Monoarthritis", "shortest_name_length": 12}
{"curie": "MONDO:0024431", "names": ["bilirubin metabolism disease", "metabolic disorder; bilirubin", "bilirubin disorder metabolism", "disorder bilirubin metabolism", "bilirubin; metabolic disorder", "Bilirubin metabolism disorder", "disorder; bilirubin-metabolism", "bilirubin disorders metabolism", "bilirubin; disorder metabolism", "Disease of bilirubin metabolism", "disorder of bilirubin metabolism", "Disorder of bilirubin metabolism", "Diseases of Bilirubin Metabolism", "DISORDERS OF BILIRUBIN METABOLISM", "Disorder of bilirubin metabolism, NOS", "Disorder of bilirubin metabolism (disorder)", "unspecified disorder of bilirubin metabolism", "disorder of bilirubin metabolism (diagnosis)", "Disorder of bilirubin metabolism, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bilirubin metabolism disease", "shortest_name_length": 28}
{"curie": "MONDO:0018776", "names": ["demyelinating HMSN", "demyelinating hereditary motor and sensory neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "demyelinating hereditary motor and sensory neuropathy", "shortest_name_length": 18}
{"curie": "MONDO:0003742", "names": ["heart fibrosarcoma", "Heart Fibrosarcoma", "cardiac fibrosarcoma", "Cardiac fibrosarcoma", "Cardiac Fibrosarcoma", "Fibrosarcoma of Heart", "fibrosarcoma of heart", "Fibrosarcoma of the Heart", "fibrosarcoma of the heart", "heart fibrosarcoma (disease)", "fibrosarcoma of heart (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heart fibrosarcoma", "shortest_name_length": 18}
{"curie": "UMLS:C3897746", "names": ["Recurrent Pilocytic Astrocytoma", "Recurrent Childhood Pilocytic Astrocytoma", "recurrent childhood pilocytic astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Pilocytic Astrocytoma", "shortest_name_length": 31}
{"curie": "UMLS:C0278487", "names": ["stage III breast cancer", "Stage III Breast Cancer", "Breast Cancer Stage III AJCC v6", "Stage III Breast Cancer AJCC v6", "Stage III Breast Carcinoma AJCC v6", "Breast Carcinoma Stage III AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Breast Cancer AJCC v6", "shortest_name_length": 23}
{"curie": "UMLS:C0854814", "names": ["Stage I Lymphoplasmacytic Lymphoma", "Ann Arbor Stage I Lymphoplasmacytic Lymphoma", "Stage I Lymphoplasmacytoid Lymphoma/Immunocytoma", "Lymphoplasmacytoid Lymphoma/Immunocytoma Stage I", "Lymphoplasmacytoid lymphoma/immunocytoma stage I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoplasmacytoid lymphoma/immunocytoma stage I", "shortest_name_length": 34}
{"curie": "MONDO:0011831", "names": ["ARVD8", "ARVC8", "arrhythmogenic right ventricular dysplasia 8", "Arrhythmogenic Right Ventricular Cardiomyopathy 8", "arrhythmogenic right ventricular cardiomyopathy 8", "ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 8", "arrhythmogenic right ventricular dysplasia type 8", "DSP arrhythmogenic right ventricular cardiomyopathy", "familial arrhythmogenic right ventricular dysplasia 8", "Arrhythmogenic Right Ventricular Dysplasia, Familial, 8", "ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 8", "arrhythmogenic right ventricular dysplasia, familial, 8", "arrhythmogenic right ventricular dysplasia, familial, type 8", "arrhythmogenic right ventricular cardiomyopathy caused by mutation in DSP"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arrhythmogenic right ventricular dysplasia 8", "shortest_name_length": 5}
{"curie": "MONDO:0016270", "names": ["low-grade neuroendocrine tumor of the corpus uteri", "low-grade neuroendocrine tumor of the uterine corpus", "well-differentiated neuroendocrine tumor of the endometrium", "well-differentiated neuroendocrine tumor of the corpus uteri", "well-differentiated neuroendocrine neoplasm of the endometrium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "low-grade neuroendocrine tumor of the corpus uteri", "shortest_name_length": 50}
{"curie": "MONDO:0019635", "names": ["Achalasia cardia", "achalasia cardia", "Primary achalasia", "primary achalasia", "idiopathic achalasia", "Idiopathic achalasia", "Idiopathic achalasia of esophagus", "idiopathic achalasia of esophagus", "Idiopathic achalasia of oesophagus", "Idiopathic achalasia of esophagus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic achalasia", "shortest_name_length": 16}
{"curie": "MONDO:0001873", "names": ["geniculate ganglionitis", "Geniculate ganglionitis", "Geniculate Ganglionitis", "Ganglionitis, Geniculate", "geniculate; ganglionitis", "ganglionitis; geniculate", "Geniculate Ganglionitides", "Ganglionitides, Geniculate", "Geniculate ganglionitis NOS", "Geniculate ganglionitis, NOS", "geniculate ganglion; neuritis", "neuritis; geniculate ganglion", "ganglion geniculatum; neuritis", "geniculate ganglion inflammation", "Geniculate ganglionitis syndrome", "Geniculate ganglionitis (disorder)", "inflammation of geniculate ganglion", "geniculate ganglionitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "geniculate ganglionitis", "shortest_name_length": 23}
{"curie": "MONDO:0005786", "names": ["Hepadnaviridae Infection", "Infection, Hepadnaviridae", "Hepadnaviridae Infections", "Infections, Hepadnaviridae", "Hepadnaviridae infectious disease", "Hepadnaviridae disease or disorder", "Hepadnaviridae caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepadnaviridae infectious disease", "shortest_name_length": 24}
{"curie": "MONDO:0100469", "names": ["ANOSMIA, ISOLATED CONGENITAL, X-LINKED", "anosmia, isolated congenital, X-linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anosmia, isolated congenital, X-linked", "shortest_name_length": 38}
{"curie": "MONDO:0020546", "names": ["Acute", "AGVHD", "acute GVHD", "Acute GVHD", "GVHD, acute", "Acute GVH disease", "acute graft vs. host disease", "Acute graft-versus-host disease", "Acute graft versus host disease", "Acute Graft Versus Host Disease", "acute graft versus host disease", "acute graft-versus-host disease", "Graft versus host disease, acute", "graft versus host disease, acute", "fulminant graft versus host disease", "Fulminant Graft Versus Host Disease", "Acute graft-versus-host disease (disorder)", "acute graft-versus-host disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute graft versus host disease", "shortest_name_length": 5}
{"curie": "MONDO:0006119", "names": ["Breast MALT lymphoma", "breast MALT lymphoma", "breast mucosa-associated lymphoid tissue lymphoma", "Breast Mucosa-Associated Lymphoid Tissue Lymphoma", "mucosa-associated lymphoid tissue (MALT) lymphoma of breast", "mucosa-associated lymphoid tissue (MALT) lymphoma of breast (diagnosis)", "Breast Extranodal Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast mucosa-associated lymphoid tissue lymphoma", "shortest_name_length": 20}
{"curie": "MONDO:0020526", "names": ["DS-AMKL", "acute megakaryoblastic leukemia in down syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute megakaryoblastic leukemia in down syndrome", "shortest_name_length": 7}
{"curie": "MONDO:0007089", "names": ["AD2", "LOFAD", "Alzheimer disease 2", "Alzheimer Disease 2", "Alzheimer disease-2", "ALZHEIMER DISEASE 2", "Alzheimer's disease 2", "Alzheimer disease type 2", "Alzheimer's disease type 2", "late onset Alzheimer disease", "Alzheimer disease 2, late onset", "ALZHEIMER DISEASE 2, LATE-ONSET", "Alzheimer Disease 2, Late-Onset", "Alzheimer disease 2, late-onset", "late-onset familial alzheimer disease", "Late onset familial Alzheimer disease", "late onset familial Alzheimer disease", "Alzheimer disease associated with APOE4", "ALZHEIMER DISEASE ASSOCIATED WITH APOE4", "Alzheimer Disease Associated With Apoe4", "Familial Alzheimer disease of late onset", "Alzheimer disease associated with APOE E4", "Familial Alzheimer's disease of late onset", "Late-onset form of familial Alzheimer disease", "Familial Alzheimer's disease of late onset (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alzheimer disease 2", "shortest_name_length": 3}
{"curie": "MONDO:0002728", "names": ["RDT", "Rhabdoid tumor", "RHABDOID TUMOR", "Rhabdoid Tumor", "rhabdoid tumor", "Rhabdoid Tumors", "rhabdoid cancer", "Tumor, Rhabdoid", "rhabdoid tumors", "Rhabdoid tumour", "Rhabdoid Sarcoma", "Rhabdoid sarcoma", "sarcoma rhabdoid", "rhabdoid sarcoma", "Tumors, Rhabdoid", "Rhabdoid tumor, NOS", "[M] Rhabdoid sarcoma", "malignant rhabdoid tumor", "Malignant rhabdoid tumor", "malignant rhabdoid tumour", "Malignant rhabdoid tumour", "Rhabdoid tumors, malignant", "Malignant rhabdoid tumor (disorder)", "Malignant rhabdoid tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rhabdoid tumor", "shortest_name_length": 3}
{"curie": "MONDO:0004311", "names": ["Cowper gland carcinoma", "carcinoma of Cowper glands", "Carcinoma of Cowper Glands", "bulbo-urethral gland carcinoma", "Adenocarcinoma of Cowper Glands", "carcinoma of bulbo-urethral gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma of Cowper glands", "shortest_name_length": 22}
{"curie": "MONDO:0032614", "names": ["EV2", "epidermodysplasia verruciformis 2", "EPIDERMODYSPLASIA VERRUCIFORMIS, SUSCEPTIBILITY TO, 2", "epidermodysplasia verruciformis, susceptibility to, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermodysplasia verruciformis, susceptibility to, 2", "shortest_name_length": 3}
{"curie": "MONDO:0003278", "names": ["inner ear cancer", "internal ear cancer", "cancer of internal ear", "malignant internal ear neoplasm", "malignant neoplasm of internal ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inner ear cancer", "shortest_name_length": 16}
{"curie": "MONDO:0044628", "names": ["SIX2-related FND", "six2-related frontonasal dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "six2-related frontonasal dysplasia", "shortest_name_length": 16}
{"curie": "MONDO:0008926", "names": ["COFS", "COFS1", "Cofs Syndrome", "COFS syndrome", "COFS SYNDROME", "Pena-Shokeir syndrome type 2", "Pena-Shokeir Syndrome, Type II", "PENA-SHOKEIR SYNDROME, TYPE II", "Cerebrooculofacioskeletal Syndrome", "Cerebrooculofacioskeletal syndrome", "cerebrooculofacioskeletal syndrome", "CEREBROOCULOFACIOSKELETAL SYNDROME 1", "Cerebrooculofacioskeletal Syndrome 1", "Cerebro-oculo-facio-skeletal syndrome", "Cerebro-Oculo-Facio-Skeletal Syndrome", "cerebro-oculo-facio-skeletal syndrome", "COFS - Cerebro-oculo-facio-skeletal syndrome", "CAMAK - Cerebro-oculo-facio-skeletal syndrome", "CAMFAK - Cerebro-oculo-facio-skeletal syndrome", "Cerebro-oculo-facio-skeletal syndrome (disorder)", "Cerebro-oculo-facio-skeletal syndrome (diagnosis)", "congenital malformations nervous system cerebro-oculo-facio-skeletal syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "COFS syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C1511303", "names": ["Breast Carcinoma with Melanotic Features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Carcinoma with Melanotic Features", "shortest_name_length": 40}
{"curie": "MONDO:0024880", "names": ["metastatic cancer", "Metastatic Cancer", "Metastatic Malignant Neoplasm", "malignant metastatic neoplasm", "metastatic malignant neoplasm", "metastatic neoplasm, malignant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metastatic malignant neoplasm", "shortest_name_length": 17}
{"curie": "UMLS:C4528557", "names": ["Stage III Breast Cancer", "Anatomic Stage III Breast Cancer AJCC v8", "Anatomic Stage III Breast Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anatomic Stage III Breast Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "UMLS:C1397452", "names": ["Pulmonary Fistula", "pulmonary fistula", "Pulmonary fistula", "fistula; pulmonary", "pulmonary; fistula", "pulmonary fistula (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pulmonary Fistula", "shortest_name_length": 17}
{"curie": "UMLS:C4527163", "names": ["Stage I Cutaneous (Skin) Melanoma", "Clinical Stage I Cutaneous Melanoma AJCC v8", "Clinical Stage I Melanoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage I Cutaneous Melanoma AJCC v8", "shortest_name_length": 33}
{"curie": "MONDO:0003965", "names": ["Capgras syndrome", "capgras syndrome", "Capgras Syndrome", "capgras' syndrome", "Capgras' syndrome", "Syndrome, Capgras", "Capgras delusion theory", "Capgras' syndrome (finding)", "Delusional misidentification syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Capgras syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0018083", "names": ["transient neonatal tyrosinemia", "transient tyrosinemia of the newborn", "transient tyrosinemia of the neonate", "tyrosine-oxidase temporary deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transient tyrosinemia of the newborn", "shortest_name_length": 30}
{"curie": "MONDO:0035783", "names": ["Non-syndromic ARM with rectoprostatic fistula", "Non-syndromic ARM with rectourethral fistula, prostatic type", "Non-syndromic anorectal malformation with rectoprostatic fistula", "non-syndromic anorectal malformation with rectourethral fistula, prostatic type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-syndromic anorectal malformation with rectourethral fistula, prostatic type", "shortest_name_length": 45}
{"curie": "UMLS:C5556450", "names": ["Endometrial Mucinous Adenocarcinoma, Gastric-Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endometrial Mucinous Adenocarcinoma, Gastric-Type", "shortest_name_length": 49}
{"curie": "UMLS:C1518703", "names": ["Ovarian Dermoid Cyst with Sebaceous Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Dermoid Cyst with Sebaceous Adenoma", "shortest_name_length": 43}
{"curie": "MONDO:0008226", "names": ["JP", "PPP", "JPD", "paradentosis", "Paradentosis", "Periodontosis", "periodontosis", "Juvenile Periodontitis", "Juvenile periodontitis", "juvenile periodontitis", "PERIODONTITIS, JUVENILE", "periodontitis, juvenile", "Periodontitis, Juvenile", "Aggressive periodontitis", "Aggressive Periodontitis", "aggressive periodontitis", "Juvenile Periodontitides", "Early-Onset Periodontitis", "periodontitis 1, juvenile", "Periodontitis, Aggressive", "Periodontitides, Juvenile", "Prepubertal periodontitis", "Prepubertal Periodontitis", "Early Onset Periodontitis", "periodontitis, prepubertal", "Periodontitis, Prepubertal", "PERIODONTITIS, PREPUBERTAL", "Periodontitis, Early-Onset", "JP - Juvenile periodontitis", "Early-Onset Periodontitides", "periodontitis, aggressive 1", "Circumpubertal Periodontitis", "PERIODONTITIS, AGGRESSIVE, 1", "periodontitis, aggressive, 1", "Periodontitides, Early-Onset", "JPD - Juvenile periodontitis", "Periodontitis, Aggressive, 1", "Periodontitis, Circumpubertal", "Rapidly progressive periodontitis", "periodontitis, aggressive, type 1", "Juvenile periodontitis (disorder)", "Aggressive periodontitis (disorder)", "aggressive periodontitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "periodontitis, aggressive 1", "shortest_name_length": 2}
{"curie": "MONDO:0004423", "names": ["central nervous system osteosarcoma", "Osteosarcoma of Central Nervous System", "osteosarcoma of central nervous system", "Osteosarcoma of the Central Nervous System", "osteosarcoma of the central nervous system", "central nervous system osteosarcoma (disease)", "central nervous system extraskeletal osteosarcoma", "Central Nervous System Extraskeletal Osteosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system extraskeletal osteosarcoma", "shortest_name_length": 35}
{"curie": "MONDO:0006030", "names": ["Cystitis chronic", "Chronic cystitis", "CHRONIC CYSTITIS", "chronic cystitis", "Chronic Cystitis", "Cystitis;chronic", "cystitis, chronic", "chronic; cystitis", "cystitis; chronic", "Cystitis chronic NOS", "Chronic cystitis NOS", "Chronic cystitis, NOS", "Other chronic cystitis", "chronic bladder infection", "BLADDER INFECTION, CHRONIC", "bladder chronic infections", "Chronic cystitis (disorder)", "chronic cystitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic cystitis", "shortest_name_length": 16}
{"curie": "MONDO:0011732", "names": ["FDAB", "familial digital arthropathy-brachydactyly", "Familial digital arthropathy-brachydactyly", "Familial Digital Arthropathy-Brachydactyly", "DIGITAL ARTHROPATHY-BRACHYDACTYLY, FAMILIAL", "Digital Arthropathy-Brachydactyly, Familial", "digital arthropathy-brachydactyly, familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial digital arthropathy-brachydactyly", "shortest_name_length": 4}
{"curie": "UMLS:C4687436", "names": ["Thymic Hepatoid Carcinoma", "Thymic Hepatoid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thymic Hepatoid Adenocarcinoma", "shortest_name_length": 25}
{"curie": "UMLS:C0404990", "names": ["Postabortal Endometritis", "Post-Abortion Endometritis", "post-abortion endometritis", "endometritis following abortion", "endometritis following abortion (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometritis following abortion", "shortest_name_length": 24}
{"curie": "UMLS:C1142536", "names": ["mrsa pneumonia", "MRSA Pneumonia", "pneumonia mrsa", "Pneumonia MRSA", "Methicillin-resistant Staphylococcus aureus pneumonia", "Methicillin-Resistant Staphylococcus aureus Pneumonia", "methicillin resistant Staphylococcus aureus pneumonia", "Methicillin resistant pneumonia due to Staphylococcus aureus", "Pneumonia due to Methicillin resistant Staphylococcus aureus", "Pneumonia due to methicillin resistant Staphylococcus aureus", "pneumonia due to methicillin-resistant Staphylococcus aureus", "Pneumonia caused by methicillin resistant Staphylococcus aureus", "pneumonia due to methicillin-resistant Staphylococcus aureus (diagnosis)", "Pneumonia caused by methicillin resistant Staphylococcus aureus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pneumonia due to methicillin resistant Staphylococcus aureus", "shortest_name_length": 14}
{"curie": "MONDO:0015253", "names": ["BDS", "DBA", "Aase syndrome", "aase syndrome", "Aase's syndrome", "congenital PRCA", "Congenital PRCA", "Diamond Blackfan", "Blackfan-Diamond", "Aase-Smith II syndrome", "Aase Smith II syndrome", "Diamond Blackfan Anemia", "Diamond-Blackfan Anemia", "diamond blackfan anemia", "anemia blackfan diamond", "Diamond Blackfan anemia", "Blackfan-Diamond anemia", "blackfan diamond anemia", "Diamond-Blackfan anemia", "Blackfan Diamond Anemia", "diamond-blackfan anemia", "Diamond Anemia, Blackfan", "diamond-blackfan anaemia", "Blackfan Diamond Disease", "Anemia, Diamond-Blackfan", "Aase syndrome (disorder)", "diamond blackfan anaemia", "Blackfan-Diamond anaemia", "Diamond-Blackfan anaemia", "anemia; Diamond-Blackfan", "Anemia, Blackfan Diamond", "Blackfan-Diamond Disease", "Anemia, Diamond Blackfan", "Diamond-Blackfan; anemia", "Diamond Blackfan anaemia", "blackfan diamond anaemia", "Aase syndrome (diagnosis)", "Diamond-Blackfan syndrome", "blackfan diamond syndrome", "erythrogenesis imperfecta", "diamond-blackfan syndrome", "blackfan-diamond syndrome", "Erythrogenesis Imperfecta", "Blackfan Diamond Syndrome", "Erythrogenesis imperfecta", "Blackfan Diamond syndrome", "Blackfan-Diamond Syndrome", "Blackfan-Diamond syndrome", "BLACKFAN-DIAMOND SYNDROME", "diamond blackfan syndrome", "Disease, Blackfan-Diamond", "Erythrogenesis Imperfectas", "Imperfecta, Erythrogenesis", "Congenital red cell aplasia", "CONGENITAL RED CELL APLASIA", "Blackfan - Diamond syndrome", "congenital red cell aplasia", "Imperfectas, Erythrogenesis", "familial hypoplastic anaemia", "inherited erythroblastopenia", "anemia Diamond Blackfan type", "Diamond-Blackfan Type Anemia", "Inherited Erythroblastopenia", "aplasia; red cell, congenital", "red cell; aplasia, congenital", "Anemia, Diamond-Blackfan Type", "Congenital hypoplastic anemia", "Inherited Erythroblastopenias", "Anemia, Diamond Blackfan Type", "Erythroblastopenia, Inherited", "congenital hypoplastic anemia", "Hypoplastic Congenital Anemia", "Anemia, Hypoplastic Congenital", "Erythroblastopenias, Inherited", "Congenital hypoplastic anaemia", "Congenital Anemia, Hypoplastic", "Hypoplastic Congenital Anemias", "Congenital Pure Red Cell Anemia", "Congenital erythroid hypoplasia", "Anemias, Hypoplastic Congenital", "Congenital pure red cell anemia", "Anemia and triphalangeal thumbs", "Congenital Anemias, Hypoplastic", "Congenital Pure Red Cell Aplasia", "Pure Hereditary Red Cell Aplasia", "congenital pure red cell aplasia", "infantile red blood cell aplasia", "Congenital pure red cell anaemia", "Congenital pure red cell aplasia", "pure red cell; anemia, congenital", "anemia; pure red cell, congenital", "Red cell aplasia, pure hereditary", "congenital; pure red cell aplasia", "Congenital (pure) red cell aplasia", "pure red cell; aplasia, congenital", "Red Cell Aplasia, Pure, Hereditary", "Congenital dyserythropoietic anemia", "Congenital dyserythropoietic anaemia", "Chronic Congenital Agenerative Anemia", "anemia congenital erythroid hypoplastic", "aregenerative anemia chronic congenital", "congenital red cell aplasia (diagnosis)", "Congenital Erythroid Hypoplastic Anemia", "Congenital hypoplastic anemia (disorder)", "Congenital anemia and triphalangeal thumbs", "Chronic constitutional pure red cell anemia", "Chronic constitutional pure red cell anaemia", "chronic constitutional pure red cell anaemia", "Chronic constitutional pure red cell aplasia", "multiple malformation syndrome aase syndrome", "infantile red blood cell aplasia (diagnosis)", "Congenital hypoplastic anemia Blackfan-Diamond type", "Congenital hypoplastic anemia, Blackfan-Diamond type", "Congenital hypoplastic anaemia Blackfan-Diamond type", "congenital red blood cell aplasia (Diamond-Blackfan)", "congenital hypoplastic anemia, Blackfan-Diamond type", "Congenital Hypoplastic Anemia of Blackfan and Diamond", "Anemia, Congenital Hypoplastic, Of Blackfan And Diamond", "Hypoplastic anemia-triphalangeal thumbs, Aase-Smith type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diamond-Blackfan anemia", "shortest_name_length": 3}
{"curie": "MONDO:0009157", "names": ["SHFM6", "SPLIT-HAND/FOOT MALFORMATION 6", "split hand-foot malformation 6", "Split-Hand-Foot Malformation 6", "split-hand/foot malformation 6", "ECTRODACTYLY, AUTOSOMAL RECESSIVE", "ectrodactyly, autosomal recessive", "Ectrodactyly, Autosomal Recessive", "split-hand/foot malformation type 6", "split hand-foot malformation type 6", "WNT10B split hand-foot malformation", "SPLIT-HAND/FOOT MALFORMATION 6 (disorder)", "split hand-foot malformation caused by mutation in WNT10B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "split hand-foot malformation 6", "shortest_name_length": 5}
{"curie": "MONDO:0010151", "names": ["Tricarboxylic Acid Cycle, Defect of", "tricarboxylic acid cycle, defect of", "TRICARBOXYLIC ACID CYCLE, DEFECT OF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tricarboxylic acid cycle, defect of", "shortest_name_length": 35}
{"curie": "MONDO:0043985", "names": ["cns sle", "CNS Lupus", "cns lupus", "CNS lupus", "lupus cns", "cns lupus erythematosus", "lupus meningoencephalitis", "meningoencephalitis, lupus", "lupus Meningoencephalitides", "lupus central nervous system", "Meningoencephalitides, lupus", "Central nervous system lupus", "Central Nervous System Lupus", "central nervous system lupus", "central nervous system lupus vasculitis", "Central Nervous System Lupus Vasculitis", "Lupus Vasculitis, Central Nervous System", "sle with central nervous system involvement", "neuropsychiatric systemic lupus erythematosus", "Central Nervous System Systemic Lupus Erythematosis", "central nervous system systemic lupus Erythematosis", "Systemic Lupus Erythematosis, Central Nervous System", "systemic lupus Erythematosis, central nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system lupus", "shortest_name_length": 7}
{"curie": "MONDO:0014912", "names": ["ORAS", "AIPDS", "OTULIPENIA", "otulipenia", "Otulipenia", "otulin deficiency", "OTULIN deficiency", "otulin-related autoinflammatory syndrome", "OTULIN-RELATED AUTOINFLAMMATORY SYNDROME", "OTULIN-related autoinflammatory syndrome", "Otulin-Related Autoinflammatory Syndrome", "autoinflammation, panniculitis and dermatosis syndrome", "AUTOINFLAMMATION, panniculitis, and dermatosis syndrome", "Autoinflammation, Panniculitis, and Dermatosis Syndrome", "AUTOINFLAMMATION, PANNICULITIS, AND DERMATOSIS SYNDROME", "Autoinflammation, panniculitis, and dermatosis syndrome", "Infantile-onset periodic fever-panniculitis-dermatosis syndrome", "infantile-onset periodic fever-panniculitis-dermatosis syndrome", "Infantile-onset periodic fever, panniculitis, dermatosis syndrome", "OTU deubiquitinase with linear linkage specificity related autoinflammatory syndrome", "OTULIN (OTU deubiquitinase with linear linkage specificity) related autoinflammatory syndrome", "OTU deubiquitinase with linear linkage specificity related autoinflammatory syndrome (disorder)", "OTU deubiquitinase with linear linkage specificity related autoinflammatory syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile-onset periodic fever-panniculitis-dermatosis syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0433905", "names": ["Spinal Cord Transection", "spinal cord transection", "Spinal Cord Transections", "Transection, Spinal Cord", "Cord Transection, Spinal", "Transections, Spinal Cord", "Cord Transections, Spinal", "Transection of spinal cord", "transection of spinal cord", "Spinal Cord transection injury", "injury spinal cord transection", "Transection of spinal cord (disorder)", "Transection of spinal cord (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spinal Cord transection injury", "shortest_name_length": 23}
{"curie": "UMLS:C1142272", "names": ["Neutrophilic dermatosis", "Neutrophilic Dermatosis", "neutrophilic dermatosis", "dermatosis; neutrophilic", "neutrophilic; dermatosis", "Neutrophilic dermatosis (disorder)", "neutrophilic dermatosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neutrophilic dermatosis", "shortest_name_length": 23}
{"curie": "MONDO:0012512", "names": ["COXPD3", "fatal mitochondrial disease due to COXPD3", "Fatal mitochondrial disease due to COXPD3", "Combined Oxidative Phosphorylation Deficiency 3", "combined oxidative phosphorylation deficiency 3", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3", "TSFM combined oxidative phosphorylation deficiency", "Combined oxidative phosphorylation deficiency type 3", "combined oxidative phosphorylation deficiency type 3", "concentric cardiomyopathy, hypotonia, and lactic acidosis", "Concentric Cardiomyopathy, Hypotonia, And Lactic Acidosis", "CONCENTRIC CARDIOMYOPATHY, HYPOTONIA, AND LACTIC ACIDOSIS", "encephalomyopathy, respiratory failure, and lactic acidosis", "Encephalomyopathy, Respiratory Failure, And Lactic Acidosis", "ENCEPHALOMYOPATHY, RESPIRATORY FAILURE, AND LACTIC ACIDOSIS", "combined oxidative phosphorylation deficiency caused by mutation in TSFM", "Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3", "fatal mitochondrial disease due to combined oxidative phosphorylation defect type 3", "Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fatal mitochondrial disease due to combined oxidative phosphorylation defect type 3", "shortest_name_length": 6}
{"curie": "MONDO:0002065", "names": ["benign breast adenomyoepithelioma", "Benign Breast Adenomyoepithelioma", "breast adenomyoepithelioma, benign", "Benign Adenomyoepithelioma of Breast", "benign adenomyoepithelioma of breast", "Benign Adenomyoepithelioma of the Breast", "benign Adenomyoepithelioma of the breast", "benign adenomyoepithelioma of the breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign breast adenomyoepithelioma", "shortest_name_length": 33}
{"curie": "MONDO:0010542", "names": ["XLCM", "CMD3B", "Cmd3b", "Dilated cardiomyopathy 3B", "Dilated Cardiomyopathy 3b", "dilated cardiomyopathy 3B", "DMD dilated cardiomyopathy", "cardiomyopathy, dilated, 3B", "CARDIOMYOPATHY, DILATED, 3B", "dilated cardiomyopathy type 3B", "X-Linked Dilated Cardiomyopathy", "X-linked dilated cardiomyopathy", "cardiomyopathy, dilated, type 3B", "CARDIOMYOPATHY, DILATED, X-LINKED", "cardiomyopathy, dilated, X-linked", "DMD-related dilated cardiomyopathy", "Dmd-Related Dilated Cardiomyopathy", "Dilated cardiomyopathy 3B (disorder)", "DMD-associated dilated cardiomyopathy", "Dmd-Associated Dilated Cardiomyopathy", "dilated cardiomyopathy caused by mutation in DMD", "Duchenne muscular dystrophy-associated dilated cardiomyopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 3B", "shortest_name_length": 4}
{"curie": "UMLS:C0854567", "names": ["Complications of transplant surgery"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Complications of transplant surgery", "shortest_name_length": 35}
{"curie": "UMLS:C5204066", "names": ["Metastatic Large Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Large Cell Neuroendocrine Carcinoma", "shortest_name_length": 46}
{"curie": "UMLS:C2698487", "names": ["Non-Neoplastic Lip Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Lip Disorder", "shortest_name_length": 27}
{"curie": "MONDO:0011356", "names": ["Subungual exostoses", "Subungual exostosis", "Subungual Exostosis", "subungual exostoses", "Dupuytren Exostosis", "Dupuytren subungual exostosis", "Exostosis, Dupuytren Subungual", "EXOSTOSIS, DUPUYTREN SUBUNGUAL", "Subungual exostosis (disorder)", "exostosis, Dupuytren subungual", "Subungual exostosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exostosis, Dupuytren subungual", "shortest_name_length": 19}
{"curie": "MONDO:0007817", "names": ["IGER", "IGEL", "ige elevated", "elevated ige", "Elevated IgE", "IgE, level of", "Increased IgE", "IGE, ELEVATED", "IgE increased", "IgE, LEVEL OF", "ige increased", "IG E INCREASED", "Ig E increased", "Elevated serum IgE", "Elevated IgE levels", "Increased IgE levels", "Immunoglobulin E high", "High immunoglobulin E", "IgE, elevated level of", "IgE, ELEVATED LEVEL OF", "ATOPIC HYPERSENSITIVITY", "Hypersensitivity type I", "atopic hypersensitivity", "Atopic Hypersensitivity", "Type 1 Hypersensitivity", "type I hypersensitivity", "Type I Hypersensitivity", "Type I hypersensitivity", "Atopic hypersensitivity", "type i hypersensitivity", "type 1 hypersensitivity", "hypersensitivity type i", "atopy, susceptibility to", "humoral hypersensitivity", "Hypersensitivity, Atopic", "Hypersensitivity, Type I", "ATOPY, SUSCEPTIBILITY TO", "Type I Hypersensitivities", "Elevated immunoglobulin E", "Atopic Hypersensitivities", "Immunoglobulin E increased", "type I immunologic disease", "Hypersensitivities, Type I", "immediate hypersensitivity", "Immediate hypersensitivity", "IgE RESPONSIVENESS, ATOPIC", "IgE responsiveness, ATOPIC", "IgE responsiveness, atopic", "Ige Responsiveness, Atopic", "Hypersensitivities, Atopic", "Immediate Hypersensitivity", "Hypersensitivity type I NOS", "Hypersensitivity, Immediate", "Hypersensitivity, immediate", "Immediate Hypersensitivities", "IgE-Mediated Hypersensitivity", "IgE Mediated Hypersensitivity", "Hypersensitivities, Immediate", "Hypersensitivity, IgE-Mediated", "IgE-mediated allergic disorder", "IgE-Mediated Hypersensitivities", "Increased circulating IgE level", "Immediate hypersensitivity, NOS", "Hypersensitivities, IgE-Mediated", "Type I Hypersensitivity Reaction", "Type I hypersensitivity disorder", "type I hypersensitivity reaction", "Type 1 Hypersensitivity Reaction", "type 1 hypersensitivity reaction", "immediate hypersensitivity response", "Immediate hypersensitivity disorder", "Immediate hypersensitivity reaction", "IgE-mediated hypersensitivity disorder", "IgE-mediated immediate hypersensitivity", "Immunoglobulin E, basic level of, in serum", "IMMUNOGLOBULIN E, BASIC LEVEL OF, IN SERUM", "Immunoglobulin E, Basic Level of, in Serum", "type I immediate hypersensitivity reaction", "Type I Immediate Hypersensitivity Reaction", "Immunoglobulin E-mediated allergic disorder", "IgE response underlying allergic asthma and rhinitis", "Ige Response Underlying Allergic Asthma and Rhinitis", "IgE RESPONSE UNDERLYING ALLERGIC ASTHMA AND RHINITIS", "Immunoglobulin E-mediated allergic disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IgE responsiveness, atopic", "shortest_name_length": 4}
{"curie": "UMLS:C0238298", "names": ["Myxedema coma", "myxedema coma", "MYXEDEMA COMA", "myxedema; coma", "coma; myxedema", "Myxoedema coma", "Hypothyroid coma", "Myxedema coma (disorder)", "myxedema coma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myxedema coma", "shortest_name_length": 13}
{"curie": "MONDO:0003082", "names": ["filamentary keratitis", "Filamentary keratitis", "filamentary; keratitis", "keratitis; filamentary", "Filamentary keratopathy", "Filamentary keratitis (disorder)", "filamentary keratitis (diagnosis)", "filamentary keratitis (physical finding)", "epithelial filamentary keratitis was observed"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "filamentary keratitis", "shortest_name_length": 21}
{"curie": "UMLS:C4521737", "names": ["Stage IVB Esophageal Squamous Cell Cancer", "Postneoadjuvant Therapy Stage IVB Esophageal Squamous Cell Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postneoadjuvant Therapy Stage IVB Esophageal Squamous Cell Carcinoma AJCC v8", "shortest_name_length": 41}
{"curie": "MONDO:0010324", "names": ["MRX81", "XLID81", "X-linked mental retardation 81", "mental retardation, X-linked 81", "Mental Retardation, X-Linked 81", "MENTAL RETARDATION, X-LINKED 81", "intellectual disability, X-linked 81", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 81", "non-syndromic X-linked intellectual disability 81", "mental retardation, X-linked 81, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 81", "shortest_name_length": 5}
{"curie": "MONDO:0017465", "names": ["congenital pseudarthrosis of the radius", "congenital pseudoarthrosis of the radius"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital pseudoarthrosis of the radius", "shortest_name_length": 39}
{"curie": "MONDO:0700082", "names": ["Robertsonian Translocation Down Syndrome", "Robertsonian translocation Down syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Robertsonian translocation Down syndrome", "shortest_name_length": 40}
{"curie": "EFO:1002012", "names": ["ligament rupture"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ligament rupture", "shortest_name_length": 16}
{"curie": "MONDO:0000970", "names": ["breast lipoma", "Breast Lipoma", "breast lipomas", "Lipoma of Breast", "Lipoma of breast", "lipoma of breast", "lipoma of the breast", "Lipoma of the Breast", "Lipoma of breast (disorder)", "Lipoma of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast lipoma", "shortest_name_length": 13}
{"curie": "UMLS:C4331479", "names": ["Unresectable Transitional Cell Cancer", "Unresectable Transitional Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Transitional Cell Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0022510", "names": ["atlantoaxial fusion", "Atlanto-Axial Fusion", "atlanto-axial fusion", "atlantoaxial joint fusion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atlanto-axial fusion", "shortest_name_length": 19}
{"curie": "MONDO:0017737", "names": ["Intermediate Salla disease", "intermediate severe Salla disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intermediate severe Salla disease", "shortest_name_length": 26}
{"curie": "MONDO:0009615", "names": ["MCEE deficiency", "methylmalonic aciduria III", "METHYLMALONIC ACIDURIA III, FORMERLY", "methylmalonic aciduria III, formerly", "methylmalonyl-Coa racemase deficiency", "METHYLMALONYL-CoA RACEMASE DEFICIENCY", "Methylmalonyl-CoA Racemase Deficiency", "methylmalonyl-CoA epimerase deficiency", "Methylmalonyl-CoA Epimerase Deficiency", "METHYLMALONYL-CoA EPIMERASE DEFICIENCY", "methylmalonic acidemia due to methylmalonyl-CoA racemase deficiency", "Methylmalonic aciduria due to methylmalonyl-CoA racemase deficiency", "methylmalonic aciduria due to methylmalonyl-CoA racemase deficiency", "Methylmalonic acidemia due to methylmalonyl-CoA racemase deficiency", "Methylmalonic aciduria due to methylmalonyl-CoA epimerase deficiency", "methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency", "Methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency", "methylmalonic aciduria due to methylmalonyl-CoA epimerase deficiency", "Methylmalonic acidaemia due to methylmalonyl-CoA racemase deficiency", "Methylmalonic acidaemia due to methylmalonyl-CoA epimerase deficiency", "Methylmalonic acidemia due to methylmalonyl-coenzyme A epimerase deficiency", "methylmalonic acidemia due to methylmalonyl-coenzyme a epimerase deficiency", "Methylmalonyl-CoA Epimerase Deficiency with Sepiapterin Reductase Deficiency", "Methylmalonic acidaemia due to methylmalonyl-coenzyme A epimerase deficiency", "methylmalonyl-Coa epimerase deficiency with sepiapterin reductase deficiency", "METHYLMALONYL-CoA EPIMERASE DEFICIENCY WITH SEPIAPTERIN REDUCTASE DEFICIENCY", "Methylmalonic acidemia due to methylmalonyl-coenzyme A epimerase deficiency (disorder)", "methylmalonic acidemia due to methylmalonyl-coenzyme a epimerase deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency", "shortest_name_length": 15}
{"curie": "MONDO:0020460", "names": ["AVWS", "Willebrand disease, acquired", "acquired von Willebrand disease", "acquired von willebrand disease", "Acquired von Willebrand disease", "acquired von Willebrand syndrome", "Acquired von Willebrand syndrome", "acquired von willebrand syndrome", "Acquired von Willebrand's disease", "Acquired Von Willebrand's disease", "vWD - Acquired von Willebrand's disease", "Acquired von Willebrand disease (disorder)", "acquired von Willebrand disease (diagnosis)", "acquired von Willebrand disease (hereditary or acquired)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired von willebrand syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0017222", "names": ["Classic PMD", "classic PMD", "Classic Pelizaeus Merzbacher Disease", "Classic Pelizaeus-Merzbacher Disease", "Pelizaeus Merzbacher Disease, Classic", "Pelizaeus-Merzbacher Disease, Classic", "Pelizaeus-Merzbacher disease, classic form", "Type I classic Pelizaeus-Merzbacher disease", "Pelizaeus-Merzbacher disease, classic form (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pelizaeus-Merzbacher disease, classic form", "shortest_name_length": 11}
{"curie": "UMLS:C4528616", "names": ["Stage I Vulvar Cancer", "Stage I Vulvar Cancer AJCC v8", "Stage I Vulvar Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Vulvar Cancer AJCC v8", "shortest_name_length": 21}
{"curie": "UMLS:C1112489", "names": ["Corneal irritation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Corneal irritation", "shortest_name_length": 18}
{"curie": "MONDO:0001684", "names": ["EPI", "Pancreatic failure", "pancreas insufficiency", "PANCREAS INSUFFICIENCY", "pancreas; insufficiency", "insufficiency; pancreas", "pancreatic insufficiency", "INSUFFICIENCY PANCREATIC", "insufficiency pancreatic", "Pancreatic insufficiency", "Pancreatic Insufficiency", "Insufficiency pancreatic", "PANCREATIC INSUFFICIENCY", "Insufficiency;pancreatic", "Insufficiency, Pancreatic", "Pancreatic Insufficiencies", "Insufficiencies, Pancreatic", "Pancreatic insufficiency, NOS", "PANCREAS INSUFFICIENCY EXOCRINE", "exocrine pancreas insufficiency", "Exocrine Pancreas Insufficiency", "exocrine pancreatic insufficiency", "pancreatic insufficiency exocrine", "Exocrine pancreatic insufficiency", "Pancreatic exocrine insufficiency", "Exocrine Pancreatic Insufficiency", "Insufficiency, Exocrine Pancreatic", "Pancreatic Insufficiency, Exocrine", "Exocrine Pancreatic Insufficiencies", "Pancreatic insufficiency (disorder)", "pancreatic insufficiency (diagnosis)", "Insufficiencies, Exocrine Pancreatic", "Pancreatic Insufficiencies, Exocrine", "Exocrine pancreatic insufficiency (EPI)", "Exocrine pancreatic insufficiency (disorder)", "Exocrine pancreatic insufficiency (diagnosis)", "Inability to properly digest food due to lack of pancreatic digestive enzymes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exocrine pancreatic insufficiency", "shortest_name_length": 3}
{"curie": "MONDO:0100278", "names": ["AGXT defect", "AGXT deficiency", "alanine glyoxylate aminotransferase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alanine glyoxylate aminotransferase deficiency", "shortest_name_length": 11}
{"curie": "UMLS:C3888796", "names": ["Intestinal angioedema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal angioedema", "shortest_name_length": 21}
{"curie": "MONDO:0025513", "names": ["Autoimmune Urticaria", "autoimmune urticaria", "Autoimmune urticaria", "Autoimmune Urticarias", "Urticaria, Autoimmune", "autoimmune urticaria (disease)", "Autoimmune urticaria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune urticaria", "shortest_name_length": 20}
{"curie": "MONDO:0030366", "names": ["CMD2E", "dilated cardiomyopathy 2E", "CARDIOMYOPATHY, DILATED, 2E", "cardiomyopathy, dilated, 2E"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiomyopathy, dilated, 2E", "shortest_name_length": 5}
{"curie": "MONDO:0016531", "names": ["digestive duplication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "digestive duplication", "shortest_name_length": 21}
{"curie": "MONDO:0009327", "names": ["heart, malformation of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heart, malformation of", "shortest_name_length": 22}
{"curie": "MONDO:0011297", "names": ["ENFL2", "nocturnal frontal lobe epilepsy 2", "epilepsy, nocturnal frontal lobe, 2", "EPILEPSY, NOCTURNAL FRONTAL LOBE, 2", "Epilepsy, Nocturnal Frontal Lobe, Type 2", "epilepsy, nocturnal frontal lobe, type 2", "autosomal dominant nocturnal frontal lobe epilepsy 2", "autosomal dominant nocturnal frontal lobe epilepsy type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nocturnal frontal lobe epilepsy 2", "shortest_name_length": 5}
{"curie": "MONDO:0012648", "names": ["IBDD", "IBD DEFICIENCY", "IBD deficiency", "ACAD8 DEFICIENCY", "Acad8 deficiency", "Isobutyric aciduria", "isobutyric aciduria", "ISOBUTYRYL-CoA DEHYDROGENASE DEFICIENCY", "isobutyryl-CoA dehydrogenase deficiency", "Isobutyryl-CoA Dehydrogenase Deficiency", "Isobutyryl-CoA dehydrogenase deficiency", "Deficiency of isobutyryl-CoA dehydrogenase", "Isobutyryl-Coenzyme A Dehydrogenase Deficiency", "Deficiency of isobutyryl-coenzyme A dehydrogenase", "Acyl-CoA dehydrogenase family, member 8, deficiency of", "ACYL-CoA DEHYDROGENASE FAMILY, MEMBER 8, DEFICIENCY OF", "acyl-Coa dehydrogenase family, member 8, deficiency of", "acyl-CoaA dehydrogenase family, member 8, deficiency of", "Deficiency of isobutyryl-coenzyme A dehydrogenase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isobutyryl-CoA dehydrogenase deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0004555", "names": ["RAML", "renal angiomyolipoma", "Renal Angiomyolipoma", "renal Angiomyolipoma", "Kidney Angiomyolipoma", "kidney angiomyolipoma", "Angiomyolipoma of Kidney", "angiomyolipoma of kidney", "Angiomyolipoma of kidney", "Angiomyolipoma of the Kidney", "angiomyolipoma of the kidney"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kidney angiomyolipoma", "shortest_name_length": 4}
{"curie": "MONDO:0017510", "names": ["adactyly of foot, bilateral", "congenital absence of toes, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adactyly of foot, bilateral", "shortest_name_length": 27}
{"curie": "UMLS:C4525865", "names": ["Stage IV Rectal Neuroendocrine Tumor", "Stage IV Rectal Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Rectal Neuroendocrine Tumor AJCC v8", "shortest_name_length": 36}
{"curie": "UMLS:C4324739", "names": ["EBVMCU", "EBV positive mucocutaneous ulcer", "EBV-Positive Mucocutaneous Ulcer", "Epstein Barr virus positive mucocutaneous ulcer", "Epstein-Barr Virus-Positive Mucocutaneous Ulcer", "Epstein Barr virus positive mucocutaneous ulcer (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "EBV positive mucocutaneous ulcer", "shortest_name_length": 6}
{"curie": "MONDO:0008472", "names": ["spondyloepiphyseal dysplasia, MacDermot type", "Spondyloepiphyseal Dysplasia, Myopia, And Sensorineural Deafness", "SPONDYLOEPIPHYSEAL DYSPLASIA, MYOPIA, AND SENSORINEURAL DEAFNESS", "spondyloepiphyseal dysplasia, myopia, and sensorineural deafness", "spondyloepiphyseal dysplasia-myopia-sensorineural deafness syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepiphyseal dysplasia, MacDermot type", "shortest_name_length": 44}
{"curie": "UMLS:C4289820", "names": ["Cervical Angiosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Angiosarcoma", "shortest_name_length": 21}
{"curie": "UMLS:C4520900", "names": ["Colorectal Cancer, Stage 0", "Stage 0 Colorectal Carcinoma", "Colorectal Carcinoma Stage 0", "Colorectal Carcinoma in situ", "Stage 0 Colorectal Cancer AJCC v7", "Stage 0 Colorectal Cancer AJCC v6", "stage 0 colorectal carcinoma in situ", "Stage 0 Colorectal Cancer AJCC v6 and v7", "Stage 0 Colorectal (Colon or Rectal) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Colorectal Cancer AJCC v6 and v7", "shortest_name_length": 26}
{"curie": "UMLS:C5239090", "names": ["SAMD9- Associated Familial MDS", "SAMD9-Associated Familial Myelodysplastic Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SAMD9-Associated Familial Myelodysplastic Syndrome", "shortest_name_length": 30}
{"curie": "UMLS:C1963823", "names": ["Hyperlipasemia", "Elevated Lipase", "Hyperlipasaemia", "Lipase increased", "Lipase Increased"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyperlipasaemia", "shortest_name_length": 14}
{"curie": "MONDO:0006858", "names": ["Oral Disease", "oral disease", "Oral disorder", "oral disorder", "mouth disease", "Mouth Disease", "Oral Disorder", "mouth disorder", "Mouth disorder", "Disease, Mouth", "mouth diseases", "Mouth Diseases", "Diseases, Mouth", "Mouth Disorders", "Mouth--Diseases", "disease of mouth", "Disease of mouth", "Disorder of mouth", "disorder of mouth", "Oral Cavity Disease", "Oral Cavity Disorder", "oral cavity disorder", "Disease of oral cavity", "Disorder of oral cavity", "mouth disease or disorder", "disease or disorder of mouth", "Disorder of mouth (disorder)", "Disorder of mouth (diagnosis)", "oral cavity disorder (diagnosis)", "disorder of upper digestive tract mouth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mouth disorder", "shortest_name_length": 12}
{"curie": "MONDO:0041167", "names": ["Carcinoid crisis", "carcinoid crisis", "Carcinoid crisis (disorder)", "carcinoid crisis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoid crisis", "shortest_name_length": 16}
{"curie": "MONDO:0003774", "names": ["Cerebral Convexity Meningioma", "cerebral convexity meningioma", "Cerebral Convexity Meningiomas", "Convexity Meningioma, Cerebral", "Meningioma, Cerebral Convexity", "Convexity Meningiomas, Cerebral", "Meningiomas, Cerebral Convexity", "cerebral hemispheric convexity meningioma", "Cerebral Hemispheric Convexity meningioma", "Cerebral Hemispheric Convexity Meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral convexity meningioma", "shortest_name_length": 29}
{"curie": "UMLS:C5446919", "names": ["DCIS - Comedo", "comedo carcinoma", "Comedocarcinoma, noninfiltrating", "Breast Intraductal Comedo Adenocarcinoma", "Breast Ductal Carcinoma In Situ, Comedo Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Ductal Carcinoma In Situ, Comedo Type", "shortest_name_length": 13}
{"curie": "MONDO:0037105", "names": ["lung germ cell tumor", "Lung Germ Cell Tumor", "lung germ cell neoplasm", "Lung Germ Cell Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung germ cell tumor", "shortest_name_length": 20}
{"curie": "MONDO:0017209", "names": ["infectious posterior uveitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infectious posterior uveitis", "shortest_name_length": 28}
{"curie": "MONDO:0008764", "names": ["LCA", "CRB", "LCA1", "Leber Congenital Amaurosis 1", "Leber congenital amaurosis 1", "LEBER CONGENITAL AMAUROSIS 1", "RETINAL BLINDNESS, CONGENITAL", "retinal blindness, congenital", "Retinal blindness, congenital", "AMAUROSIS CONGENITA OF LEBER I", "amaurosis congenita of Leber I", "amaurosis congenita of Leber 1", "Amaurosis Congenita Of Leber I", "Leber congenital amaurosis type 1", "GUCY2D Leber congenital amaurosis", "Leber congenital amaurosis, type 1", "amaurosis congenita of Leber, type 1", "Amaurosis congenita of Leber, type 1", "Leber congenital amaurosis caused by mutation in GUCY2D"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leber congenital amaurosis 1", "shortest_name_length": 3}
{"curie": "UMLS:C4329255", "names": ["Acquired Factor III Deficiency", "Acquired Tissue Factor Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired Factor III Deficiency", "shortest_name_length": 30}
{"curie": "UMLS:C4744715", "names": ["Locally Advanced Prostate Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Prostate Adenocarcinoma", "shortest_name_length": 40}
{"curie": "UMLS:C1698675", "names": ["anastomotic leak ureter", "ureteric anastomotic leak", "Ureteric anastomotic leak", "Ureteral Anastomotic Leak", "Ureteric Anastomotic Leakage", "ureteric anastomotic leak (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ureteric Anastomotic Leakage", "shortest_name_length": 23}
{"curie": "UMLS:C5554629", "names": ["Recurrent Low Grade Glioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Low Grade Glioma", "shortest_name_length": 26}
{"curie": "MONDO:0010358", "names": ["CLCN5 X-linked hypophosphatemic rickets", "X-linked recessive hypophosphatemic rickets", "HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE", "Hypophosphatemic Rickets, X-Linked Recessive", "hypophosphatemic rickets, X-linked recessive", "Hypophosphatemic Rickets, X Linked Recessive", "X-linked hypophosphatemic rickets caused by mutation in CLCN5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypophosphatemic rickets, X-linked recessive", "shortest_name_length": 39}
{"curie": "UMLS:C2981669", "names": ["Stage IV Distal Bile Duct Cancer", "stage IV distal bile duct cancer", "Stage IV Distal Bile Duct Cancer AJCC v7", "stage IV distal bile duct cancer AJCC v7", "stage IV distal extrahepatic bile duct cancer", "Stage IV Extrahepatic (Distal) Bile Duct Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Distal Bile Duct Cancer AJCC v7", "shortest_name_length": 32}
{"curie": "UMLS:C2986685", "names": ["stage III AIDS-related lymphoma", "Stage III AIDS-Related Lymphoma", "Ann Arbor Stage III AIDS-Related Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage III AIDS-Related Lymphoma", "shortest_name_length": 31}
{"curie": "MONDO:0027091", "names": ["xanthogranulomatous sialadenitis", "Xanthogranulomatous sialadenitis", "sialadenitis, xanthogranulomatous", "Sialadenitis, xanthogranulomatous", "xanthogranulomatous salivary gland disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "xanthogranulomatous sialadenitis", "shortest_name_length": 32}
{"curie": "UMLS:C1960396", "names": ["EGFR negative non-small cell lung cancer", "EGF-R negative non-small cell lung cancer", "Epidermal growth factor receptor negative non-small cell lung cancer", "Non-small cell lung cancer, negative for epidermal growth factor receptor expression", "Non-small cell lung cancer, negative for epidermal growth factor receptor expression (disorder)", "Non-small cell lung cancer, negative for epidermal growth factor receptor expression (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epidermal growth factor receptor negative non-small cell lung cancer", "shortest_name_length": 40}
{"curie": "MONDO:0007253", "names": ["CANCER, FAMILIAL, WITH IN VITRO RADIORESISTANCE", "Cancer, Familial, with In Vitro Radioresistance", "cancer, familial, with in vitro Radioresistance", "cancer, familial, with in vitro RADIORESISTANCE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cancer, familial, with in vitro Radioresistance", "shortest_name_length": 47}
{"curie": "MONDO:0017289", "names": ["flit", "fetal lung interstitial tumor", "immature interstitial mesenchymal tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fetal lung interstitial tumor", "shortest_name_length": 4}
{"curie": "MONDO:0006153", "names": ["Colon Juvenile Polyp", "colon juvenile polyp", "colon retention polyp", "Colon Retention Polyp", "Colonic Juvenile Polyp", "colonic juvenile polyp", "Colonic Retention Polyp", "colonic retention polyp", "Juvenile Polyp of Colon", "juvenile polyp of colon", "Retention Polyp of Colon", "retention polyp of colon", "Juvenile Polyp of the Colon", "juvenile polyp of the colon", "retention polyp of the colon", "Retention Polyp of the Colon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colon juvenile polyp", "shortest_name_length": 20}
{"curie": "MONDO:0010986", "names": ["NRSD9", "AUNB1", "DFNB9", "NSRD9", "NSRAN", "autosomal recessive deafness 9", "deafness, autosomal recessive 9", "Deafness, Autosomal Recessive 9", "DEAFNESS, AUTOSOMAL RECESSIVE 9", "deafness, autosomal recessive type 9", "auditory neuropathy, nonsyndromic recessive", "AUDITORY NEUROPATHY, NONSYNDROMIC RECESSIVE", "AUDITORY NEUROPATHY, AUTOSOMAL RECESSIVE, 1", "Auditory Neuropathy, Nonsyndromic Recessive", "Auditory Neuropathy, Autosomal Recessive, 1", "auditory neuropathy, autosomal recessive, 1", "autosomal recessive nonsyndromic deafness 9", "Neurosensory Nonsyndromic Recessive Deafness 9", "neurosensory nonsyndromic recessive deafness 9", "OTOF autosomal recessive nonsyndromic deafness", "NEUROSENSORY NONSYNDROMIC RECESSIVE DEAFNESS 9", "autosomal recessive nonsyndromic hearing loss 9", "autosomal recessive nonsyndromic deafness type 9", "autosomal recessive nonsyndromic deafness caused by mutation in OTOF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 9", "shortest_name_length": 5}
{"curie": "UMLS:C4744726", "names": ["Locally Advanced Unresectable Cervical Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Unresectable Cervical Adenocarcinoma", "shortest_name_length": 53}
{"curie": "MONDO:0014220", "names": ["MMDD", "AMPD1 DEFICIENCY", "AMPD1 deficiency", "AMP deaminase deficiency", "AMP deaminase 1 deficiency", "myoadenylate deaminase deficiency", "adenosine monophosphate deaminase deficiency", "adenosine monophosphate deaminase 1 deficiency", "myopathy due to myoadenylate deaminase deficiency", "MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY", "Myopathy due to Myoadenylate Deaminase Deficiency", "myoadenylate deaminase deficiency, myopathy due to", "MYOADENYLATE DEAMINASE DEFICIENCY, MYOPATHY DUE TO", "adenosine monophosphate deaminase-1 deficiency, myopathy due to", "ADENOSINE MONOPHOSPHATE DEAMINASE-1 DEFICIENCY, MYOPATHY DUE TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy due to myoadenylate deaminase deficiency", "shortest_name_length": 4}
{"curie": "UMLS:C4527554", "names": ["HHV8-Positive DLBCL, NOS", "HHV8-Positive Diffuse Large B-Cell Lymphoma, NOS", "HHV8-Positive Diffuse Large B-Cell Lymphoma, Not Otherwise Specified", "Human Herpesvirus 8-Positive Diffuse Large B-Cell Lymphoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HHV8-Positive Diffuse Large B-Cell Lymphoma, Not Otherwise Specified", "shortest_name_length": 24}
{"curie": "MONDO:0024462", "names": ["familial cutaneous melanoma", "hereditary cutaneous melanoma (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial cutaneous melanoma", "shortest_name_length": 27}
{"curie": "MONDO:0004247", "names": ["GDU", "PUD", "pud", "Ulcer;peptic", "Peptic ulcer", "ULCER PEPTIC", "PEPTIC ULCER", "Ulcer peptic", "peptic ulcer", "Peptic Ulcer", "peptic; ulcer", "Ulcer, Peptic", "ulcer; peptic", "Peptic Ulcers", "Ulcer disease", "Ulcer, peptic", "peptic ulcers", "Ulcers, Peptic", "peptic ulcer nos", "peptic ulcer NOS", "Peptic ulceration", "PU - Peptic ulcer", "Peptic ulcer, NOS", "peptic ulcer disease", "ULCER GASTRODUODENAL", "Peptic ulcer disease", "gastroduodenal ulcer", "Ulcer gastroduodenal", "Gastroduodenal ulcer", "Peptic Ulcer (Ulcer)", "Peptic Ulcer Disease", "Gastroduodenal Ulcer", "PEPTIC ULCER DISEASE", "Ulcer, Gastroduodenal", "Gastroduodenal Ulcers", "Ulcer syndrome peptic", "ULCER SYNDROME PEPTIC", "SYNDROME PEPTIC ULCER", "peptic ulcer disorder", "PEPTIC ULCER SYNDROME", "Peptic ulcer syndrome", "Syndrome peptic ulcer", "Ulcers, Gastroduodenal", "Peptic ulcer (disorder)", "gastroduodenal ulcer NOS", "peptic ulcer (diagnosis)", "Gastroduodenal ulcer, NOS", "PUD - Peptic ulcer disease", "Peptic ulcer; site unspecified", "Peptic ulcer, site unspecified", "acute peptic ulcer with hemorrhage", "ulcer of the gastrointestinal tract", "Sore in the lining of gastrointestinal tract", "acute peptic ulcer with hemorrhage and perforation", "acute peptic ulcer without hemorrhage and without perforation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peptic ulcer disease", "shortest_name_length": 3}
{"curie": "MONDO:0044787", "names": ["Sinonasal Squamous Cell Carcinoma", "nasal cavity and paranasal sinus squamous cell cancer", "Nasal Cavity and Paranasal Sinus Squamous Cell Cancer", "epidermoid carcinoma, paranasal sinus and nasal cavity", "Squamous cell carcinoma of the nasal cavity and sinuses", "paranasal sinus and nasal cavity squamous cell carcinoma", "Nasal Cavity and Paranasal Sinus Squamous Cell Carcinoma", "nasal cavity and paranasal sinus squamous cell carcinoma", "squamous cell carcinoma, paranasal sinus and nasal cavity", "paranasal sinus and nasal cavity cancer squamous cell carcinoma", "nasal cavity and paranasal sinus cancer squamous cell carcinoma", "Squamous cell carcinoma of the nasal cavity and paranasal sinuses"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasal cavity and paranasal sinus squamous cell carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0003434", "names": ["vagina adenoma", "vaginal adenoma", "Vaginal Adenoma", "Vaginal Adenomatous Polyp", "Vaginal Intestinal-Type Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vaginal adenoma", "shortest_name_length": 14}
{"curie": "MONDO:0002343", "names": ["Spleen Angioma", "spleen angioma", "splenic angioma", "Splenic Angioma", "spleen hemangioma", "Spleen Hemangioma", "angioma of spleen", "Spleen hemangioma", "hemangioma spleen", "Angioma of Spleen", "Splenic hemangioma", "splenic hemangioma", "Splenic Hemangioma", "Hemangioma of Spleen", "Hemangioma of spleen", "hemangioma of spleen", "Angioma of the Spleen", "angioma of the spleen", "Haemangioma of spleen", "hemangioma of the spleen", "Hemangioma of the Spleen", "benign hemangioma of spleen", "Hemangioma of spleen (disorder)", "benign hemangioma of spleen (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "splenic hemangioma", "shortest_name_length": 14}
{"curie": "UMLS:C4725623", "names": ["High Grade Myeloid Neoplasm", "High-Grade Myeloid Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Myeloid Neoplasm", "shortest_name_length": 27}
{"curie": "UMLS:C5555136", "names": ["Conventional Chordoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conventional Chordoma", "shortest_name_length": 21}
{"curie": "MONDO:0015002", "names": ["DEE49", "EIEE49", "early infantile epileptic encephalopathy 49", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 49", "epileptic encephalopathy, early infantile, 49", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 49", "developmental and epileptic encephalopathy 49", "developmental and epileptic encephalopathy, 49", "DENND5A early infantile epileptic encephalopathy", "epileptic encephalopathy, early infantile, type 49", "epileptic encephalopathy, early infantile, 49; EIEE49", "early infantile epileptic encephalopathy caused by mutation in DENND5A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 49", "shortest_name_length": 5}
{"curie": "UMLS:C2939062", "names": ["Respiratory tract edema", "Respiratory tract oedema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Respiratory tract edema", "shortest_name_length": 23}
{"curie": "MONDO:0001858", "names": ["Tietze", "Tietze disease", "COSTOCHONDRITIS", "costochondritis", "Tietze Syndrome", "tietze syndrome", "Costochondritis", "Tietze syndrome", "TIETZE SYNDROME", "chostochondritis", "Tietzes Syndrome", "tietze's disease", "Tietze's disease", "Costalchondritis", "costalchondritis", "Tietzes syndrome", "Tietze's syndrome", "costal chondritis", "tietze's syndrome", "Costal Chondritis", "COSTAL CHONDRITIS", "Costal chondritis", "TIETZE'S SYNDROME", "Cyriax's syndrome", "Tietze's Syndrome", "Syndrome, Tietze's", "costal; chondritis", "chondritis; costal", "Chondritis, Costal", "Costal Chondritides", "costal chondritides", "Chondritides, Costal", "Costochondritis, NOS", "Costalchondritis, NOS", "slipping rib syndrome", "Slipping rib syndrome", "CHONDROPATHIA TUBEROSA", "chondropathia tuberosa", "Chondropathia tuberosa", "costal; chondritis, Tietze", "Peristernal perichondritis", "chondritis; costal, Tietze", "costochondritis (diagnosis)", "Tietze's disease (disorder)", "Costal chondritis (disorder)", "Chondrocostal junction syndrome", "Costochondral junction syndrome", "chondrocostal junction syndrome", "costochondral junction syndrome", "COSTOCHONDRAL JUNCTION SYNDROME", "syndrome; chondrocostal junction", "chondrocostal junction; syndrome", "costochondral junction; syndrome", "syndrome; costochondral junction", "costochondritis (Tietze's syndrome)", "costochondral joint syndromic disease", "overlap syndrome; chondrocostal (Tietze)", "Chondrocostal junction syndrome [Tietze]", "syndromic disease of costochondral joint", "Musculoskeletal chest pain due to costochondral junction syndrome", "Musculoskeletal Chest Pain due to Costochondral Junction Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tietze syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C5236088", "names": ["Metastatic Malignant PEComa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Malignant PEComa", "shortest_name_length": 27}
{"curie": "MONDO:0020408", "names": ["CAVC type C", "CAVC-Fallot tetralogy syndrome", "complete atrioventricular canal type C", "complete atrioventricular canal-tetralogy of fallot syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complete atrioventricular canal-tetralogy of fallot syndrome", "shortest_name_length": 11}
{"curie": "UMLS:C3539781", "names": ["Progressive cGVHD", "Progressive Disease", "Progressive chronic Graft vs Host Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Progressive cGVHD", "shortest_name_length": 17}
{"curie": "UMLS:C1515866", "names": ["Prostate Acinar Adenocarcinoma, Pseudohyperplastic Variant", "Acinar Prostate Adenocarcinoma, Pseudohyperplastic Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Acinar Adenocarcinoma, Pseudohyperplastic Variant", "shortest_name_length": 58}
{"curie": "UMLS:C1707434", "names": ["Colon Intramucosal Neoplasia", "Colon Intramucosal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colon Intramucosal Adenocarcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0010775", "names": ["RP8, formerly", "RP21, formerly", "retinitis pigmentosa 8", "retinitis pigmentosa 21", "retinitis pigmentosa 8, formerly", "retinitis pigmentosa 21, formerly", "retinitis pigmentosa-deafness syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa-deafness syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0015537", "names": ["NXG", "Necrobiotic Xanthogranuloma", "necrobiotic xanthogranuloma", "Necrobiotic xanthogranuloma", "Necrobiotic Xanthogranulomas", "Xanthogranuloma, Necrobiotic", "Xanthogranulomas, Necrobiotic", "Necrobiotic xanthogranuloma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "necrobiotic xanthogranuloma", "shortest_name_length": 3}
{"curie": "UMLS:C1328381", "names": ["Chronic left ventricular failure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic left ventricular failure", "shortest_name_length": 32}
{"curie": "UMLS:C4763763", "names": ["Recurrent Adenoid Cystic Cancer", "Recurrent Adenoid Cystic Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Adenoid Cystic Carcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C0161679", "names": ["ethylism", "alcohol poison", "poison alcohol", "ALCOHOL OVERDOSE", "overdose alcohol", "alcohol overdose", "Ethanol poisoning", "alcohol poisoning", "poisoning ethanol", "poisoning alcohol", "Alcohol poisoning", "ethanol poisoning", "alcohol overdoses", "poisoning; alcohol", "alcohol; poisoning", "alcohol poisonings", "poisoning by alcohol", "Ethanol intoxication", "Toxic effect of ethanol", "Ethyl alcohol poisoning", "poisoning by ethyl alcohol", "Toxic effect of ethanol NOS", "Ethanol causing toxic effect", "Toxic effect of grain alcohol", "Toxic effect of ethyl alcohol", "poisoning by alcohol (diagnosis)", "Ethyl alcohol causing toxic effect", "poisoning by ethyl alcohol (diagnosis)", "Toxic effect of ethyl alcohol (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Toxic effect of ethyl alcohol", "shortest_name_length": 8}
{"curie": "MONDO:0019347", "names": ["PSS", "deciduous skin", "peeling skin disease", "peeling skin syndrome", "skin peeling syndrome", "keratolysis exfoliativa", "Keratolysis exfoliativa", "Idiopathic deciduous skin", "idiopathic deciduous skin", "keratosis exfoliativa congenita", "Familial continual skin peeling", "familial continuous skin peeling", "Keratolysis exfoliativa (disorder)", "Keratolysis exfoliativa congenital", "familial continuous skin peeling syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peeling skin syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C4054154", "names": ["Primary Bone Non-Hodgkin Lymphoma", "Primary Non-Hodgkin Lymphoma of Bone", "Primary Non-Hodgkin Lymphoma of the Bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Bone Non-Hodgkin Lymphoma", "shortest_name_length": 33}
{"curie": "UMLS:C2111730", "names": ["Liver Large Cell Neuroendocrine Carcinoma", "Hepatic Large Cell Neuroendocrine Carcinoma", "large cell neuroendocrine carcinoma of liver", "large cell neuroendocrine carcinoma of liver (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "large cell neuroendocrine carcinoma of liver", "shortest_name_length": 41}
{"curie": "MONDO:0017231", "names": ["erythropoietic uroporphyria associated with myeloid malignancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythropoietic uroporphyria associated with myeloid malignancy", "shortest_name_length": 62}
{"curie": "MONDO:0002388", "names": ["Intracystic papilloma", "Intracystic Papilloma", "intracystic papilloma", "Breast Intracystic Papilloma", "Intracystic papillary adenoma", "Intracystic Papillary Adenoma", "intracystic papillary adenoma", "Intracystic papillary adenoma (morphologic abnormality)", "intracystic papillary adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intracystic papillary adenoma", "shortest_name_length": 21}
{"curie": "UMLS:C3272610", "names": ["Colorectal NET", "Colorectal Neuroendocrine Tumor", "Large Intestinal Neuroendocrine Tumor", "Colorectal Well Differentiated Endocrine Tumor", "Colorectal Well Differentiated Endocrine Tumor/Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Neuroendocrine Tumor", "shortest_name_length": 14}
{"curie": "MONDO:0004664", "names": ["WORM", "Worms", "worms", "Worms NOS", "Worms, NOS", "helminthosis", "Helminthosis", "HELMINTHIASES", "HELMINTHIASIS", "Helminthiases", "helminthiases", "Helminthiasis", "helminthiasis", "worm infection", "Worm infection", "worm infestation", "Worm infestation", "worms; infection", "infection; worms", "worms infestation", "Helminthiasis NOS", "infestation; worms", "helminth infection", "worms; infestation", "Helminth infection", "helminth infections", "Helminthic infection", "helminthic infection", "helminthes; infection", "infection; helminthes", "helminthic infections", "Infestation (by);worms", "Helminthiases (B65-B83)", "Helminth infection, NOS", "helminthes; infestation", "infestation; helminthes", "Helminthic infection NOS", "helminthiasis (diagnosis)", "Helminthiasis, unspecified", "helminth parasite infection", "HELMINTHIC INFECTIOUS DISEASES", "Helminth infection, unspecified", "HELMINTHIC INFECTIONS: GENERAL TERMS", "parasitic helminthiasis infectious disease", "Infection due to Class Cestoda and/or Class Trematoda and/or Phylum Nemata", "Infection caused by Class Cestoda and/or Class Trematoda and/or Phylum Nemata", "Infection caused by Class Cestoda and/or Class Trematoda and/or Phylum Nemata (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "helminthiasis", "shortest_name_length": 4}
{"curie": "MONDO:0000665", "names": ["apraxia", "Apraxia", "Apraxias", "dyspraxia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "apraxia", "shortest_name_length": 7}
{"curie": "UMLS:C5420388", "names": ["Non-Neoplastic Tongue Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Tongue Disorder", "shortest_name_length": 30}
{"curie": "MONDO:0016875", "names": ["partial deletion of chromosome 10", "partial monosomy of chromosome 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of chromosome 10", "shortest_name_length": 33}
{"curie": "MONDO:0001880", "names": ["median rhomboid glossitis", "Median rhomboid glossitis", "persistent tuberculum impar", "Persistent tuberculum impar", "Glossitis rhomboidea mediana", "Superficial midline glossitis", "median rhomboid glossitis (diagnosis)", "Persistent tuberculum impar (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "median rhomboid glossitis", "shortest_name_length": 25}
{"curie": "UMLS:C0877042", "names": ["loss graft", "graft loss", "Graft loss"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Graft loss", "shortest_name_length": 10}
{"curie": "MONDO:0011221", "names": ["Weyers ulnar ray/oligodactyly syndrome", "WEYERS ULNAR RAY/OLIGODACTYLY SYNDROME", "Weyers ulnar ray-oligodactyly syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Weyers ulnar ray/oligodactyly syndrome", "shortest_name_length": 38}
{"curie": "MONDO:0019837", "names": ["atrial auricle anomaly", "atrial appendage anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial appendage anomaly", "shortest_name_length": 22}
{"curie": "MONDO:0009445", "names": ["Dykes-Marks-Harper syndrome", "Dykes-Markes-Harper syndrome", "Dykes Markes Harper syndrome", "Ichthyosis hepatosplenomegaly cerebellar degeneration", "Ichthyosis, cerebellar degeneration and hepatosplenomegaly", "ICHTHYOSIS, HEPATOSPLENOMEGALY, AND CEREBELLAR DEGENERATION", "ichthyosis, hepatosplenomegaly, and cerebellar degeneration", "Ichthyosis, hepatosplenomegaly, and cerebellar degeneration", "Ichthyosis-hepatosplenomegaly-cerebellar degeneration syndrome", "ichthyosis-hepatosplenomegaly-cerebellar degeneration syndrome", "Ichthyosis, cerebellar degeneration and hepatosplenomegaly (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ichthyosis-hepatosplenomegaly-cerebellar degeneration syndrome", "shortest_name_length": 27}
{"curie": "MONDO:0700194", "names": ["Chicken Lymphoma", "chicken lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chicken lymphoma", "shortest_name_length": 16}
{"curie": "MONDO:0009411", "names": ["APS1", "PGA I", "PGA 1", "APS I", "APS 1", "APECED", "APEDED", "APS Type 1", "APS type 1", "HAM syndrome", "ham syndrome", "MEDAC syndrome", "APECED syndrome", "AIRE Deficiency", "APECED Syndrome", "Whitaker syndrom", "Deficiency, AIRE", "blizzard syndrome", "AIRE Deficiencies", "Whitaker syndrome", "Blizzard syndrome", "Juvenile familial endocrinopathy", "aire autoimmune polyendocrinopathy", "ENDOCRINOPATHY, FAMILIAL, JUVENILE", "AIRE autoimmune polyendocrinopathy", "Autoimmune Polyglandular Syndrome I", "Candidiasis-endocrinopathy syndrome", "autoimmune polyglandular syndrome I", "Autoimmune polyendocrinopathy type 1", "autoimmune polyendocrinopathy type 1", "Autoimmune polyendocrine syndrome type 1", "Polyglandular autoimmune syndrome type I", "Autoimmune polyglandular syndrome type 1", "autoimmune polyendocrine syndrome type 1", "Autoimmune Polyglandular Syndrome Type 1", "autoimmune polyglandular syndrome type 1", "Polyglandular Autoimmune Syndrome Type 1", "Autoimmune Polyendocrine Syndrome Type 1", "Autoimmune Polyglandular Syndrome Type I", "polyglandular autoimmune syndrome type 1", "autoimmune polyendocrine syndrome type I", "Polyglandular Type I Autoimmune Syndrome", "Autoimmune Syndrome Type I, Polyglandular", "Autoimmune Polyglandular Syndrome, Type 1", "autoimmune polyglandular syndrome, type 1", "Polyglandular Autoimmune Syndrome, Type I", "POLYGLANDULAR AUTOIMMUNE SYNDROME, TYPE I", "polyglandular autoimmune syndrome, type 1", "Polyglandular Autoimmune Syndrome, Type 1", "Polyglandular autoimmune syndrome, type 1", "Autoimmune Polyglandular Syndrome, Type I", "AUTOIMMUNE POLYGLANDULAR SYNDROME, TYPE I", "Polyglandular autoimmune syndrome - type 1", "Type 1 polyendocrine autoimmunity syndrome", "Autoimmune Polyendocrinopathy Syndrome Type 1", "autoimmune polyendocrinopathy syndrome type 1", "Hypoparathyroidism, Addison's disease AND moniliasis", "Polyglandular autoimmune syndrome, type 1 (disorder)", "Hypoparathyroidism, Addison's disease and moniliasis", "autoimmune polyendocrine syndrome type I (diagnosis)", "Polyglandular Deficiency Syndrome, Persian-Jewish Type", "polyglandular deficiency syndrome, Persian-Jewish type", "POLYGLANDULAR DEFICIENCY SYNDROME, PERSIAN-JEWISH TYPE", "autoimmune polyendocrinopathy caused by mutation in AIRE", "autoimmune polyendocrinopathy caused by mutation in aire", "Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy", "AUTOIMMUNE POLYENDOCRINOPATHY-CANDIDIASIS-ECTODERMAL DYSTROPHY", "Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal-Dystrophy", "autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy", "Autoimmune Polyendocrinopathy Candidiasis Ectodermal Dystrophy", "Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy", "Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy, Autoimmune", "Polyendocrinopathy-Candidiasis-Ectodermal-Dystrophy, Autoimmune", "Polyendocrinopathy Candidiasis Ectodermal Dystrophy, Autoimmune", "AUTOIMMUNE POLYENDOCRINOPATHY SYNDROME, TYPE I, AUTOSOMAL DOMINANT", "Polyglandular deficiency associated with mucocutaneous candidiasis", "autoimmune polyendocrinopathy syndrome, type I, autosomal dominant", "Multiple endocrine deficiency-Addison disease-candidiasis syndrome", "multiple endocrine deficiency-Addison disease-candidiasis syndrome", "Autoimmune polyendocrinopathy, candidosis AND ectodermal dystrophy", "Autoimmune Polyendocrinopathy Syndrome, Type I, Autosomal Dominant", "Autoimmune polyendocrinopathy, candidosis and ectodermal dystrophy", "Hypoadrenocorticism, hypoparathyroidism and superficial moniliasis", "Hypoparathyroidism-Addison disease-mucocutaneous candidiasis syndrome", "hypoparathyroidism-Addison disease-mucocutaneous candidiasis syndrome", "HYPOADRENOCORTICISM WITH HYPOPARATHYROIDISM AND SUPERFICIAL MONILIASIS", "hypoadrenocorticism with hypoparathyroidism and superficial Moniliasis", "autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome", "Autoimmune Polyendocrinopathy with Candidiasis and Ectodermal Dystrophy", "Autoimmune Polyendocrinopathy-candidiasis-ectodermal Dystrophy Syndrome", "APECED - Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy", "Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome", "autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED)", "Autoimmune hypoparathyroidism-chronic candidiasis-Addison disease syndrome", "autoimmune hypoparathyroidism-chronic candidiasis-Addison disease syndrome", "autoimmune polyendocrine syndrome, type I, with or without reversible metaphyseal dysplasia", "AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I, WITH OR WITHOUT REVERSIBLE METAPHYSEAL DYSPLASIA", "autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune polyendocrine syndrome type 1", "shortest_name_length": 4}
{"curie": "UMLS:C0013927", "names": ["Embolus amniotic fluid", "EMBOLUS AMNIOTIC FLUID", "amniotic fluid embolus", "Amniotic fluid embolus", "amniotic embolism fluid", "Embolus, amniotic fluid", "Amniotic fluid syndrome", "amniotic fluid embolism", "Amniotic Fluid Embolism", "Amniotic fluid embolism", "EMBOLISM, AMNIOTIC FLUID", "embolism; amniotic fluid", "amniotic fluid; embolism", "Amniotic Fluid Embolisms", "Embolism, Amniotic Fluid", "Embolisms, Amniotic Fluid", "Amniotic Fluid Embolism Syndrome", "Amniotic fluid embolism syndrome", "Amniotic fluid embolism (disorder)", "embolism; obstetric, amniotic fluid", "amniotic fluid; embolism, obstetric", "amniotic fluid embolism (diagnosis)", "obstetric; embolism, amniotic fluid", "Amniotic fluid embolus (morphologic abnormality)", "Amniotic fluid embolism, unspecified as to episode of care", "Amniotic fluid embolism, unspecified as to episode of care or not applicable"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Embolism, Amniotic Fluid", "shortest_name_length": 22}
{"curie": "MONDO:0016853", "names": ["r(Y)", "ring chromosome Y", "Ring chromosome Y", "Ring chromosome type Y", "Ring chromosome Y syndrome", "Ring chromosome Y syndrome (disorder)", "Ring chromosome Y syndrome (diagnosis)", "anomaly of chromosome y ring chromosome syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ring chromosome Y", "shortest_name_length": 4}
{"curie": "UMLS:C0278854", "names": ["stage IV follicular thyroid cancer", "follicular thyroid cancer, stage IV", "thyroid cancer, stage IV follicular", "metastatic follicular thyroid cancer", "thyroid cancer, metastatic follicular", "follicular thyroid cancer, metastatic", "carcinoma, follicular, thyroid, stage IV", "Stage IV Thyroid Gland Follicular Cancer", "carcinoma, follicular, thyroid, metastatic", "Stage IV Thyroid Gland Follicular Carcinoma", "follicular carcinoma of the thyroid, stage IV", "follicular carcinoma of the thyroid, metastatic", "Stage IV Thyroid Gland Follicular Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Thyroid Gland Follicular Carcinoma AJCC v7", "shortest_name_length": 34}
{"curie": "UMLS:C0936243", "names": ["HIV-1 Cognitive and Motor Complex", "HIV 1 Cognitive and Motor Complex", "HIV 1 Associated Cognitive Motor Complex", "HIV-1-Associated Cognitive Motor Complex"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HIV-1-Associated Cognitive Motor Complex", "shortest_name_length": 33}
{"curie": "MONDO:0000978", "names": ["extrahepatic bile duct lipoma", "Extrahepatic Bile Duct Lipoma", "lipoma of extrahepatic bile duct", "Lipoma of Extrahepatic Bile Duct", "Lipoma of the Extrahepatic Bile Duct", "lipoma of the extrahepatic bile duct", "Lipoma of the extrahepatic bile duct", "lipoma of extrahepatic bile duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extrahepatic bile duct lipoma", "shortest_name_length": 29}
{"curie": "UMLS:C0858970", "names": ["carcinogenicity", "Carcinogenicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carcinogenicity", "shortest_name_length": 15}
{"curie": "UMLS:C4528210", "names": ["BIA-ALCL", "Breast Implant-Associated Anaplastic Large Cell Lymphoma", "lymphoma anaplastic large cell breast implant associated", "Breast implant-associated anaplastic large cell lymphoma", "breast implant associated anaplastic large cell lymphoma", "Breast implant-associated anaplastic large-cell lymphoma", "Breast implant associated anaplastic large cell lymphoma (BIA-ALCL)", "Breast Implant Associated Anaplastic Large Cell Lymphoma (BIA ALCL)", "Breast implant-associated anaplastic large-cell lymphoma (disorder)", "BIA-ALCL - breast implant-associated anaplastic large-cell lymphoma", "breast implant associated anaplastic large cell lymphoma (diagnosis)", "Breast Implant-Associated Anaplastic Large Cell Lymphoma, ALK-Negative", "Breast implant-associated anaplastic large cell lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast implant-associated anaplastic large cell lymphoma", "shortest_name_length": 8}
{"curie": "MONDO:0018888", "names": ["congenital cornea plana"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital cornea plana", "shortest_name_length": 23}
{"curie": "UMLS:C5230531", "names": ["PEM", "Epithelioid Blue Nevus", "Pigmented Epithelioid Melanocytoma", "Pigmented epithelioid melanocytoma", "Pigmented epithelioid melanocytoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pigmented epithelioid melanocytoma", "shortest_name_length": 3}
{"curie": "MONDO:0024562", "names": ["SSS1", "sick sinus syndrome 1", "SCN5A sick sinus syndrome", "sick sinus syndrome, congenital", "sinus rhythm, congenital absence of", "sinus bradycardia syndrome, familial", "sick sinus syndrome caused by mutation in SCN5A", "sinus node disease, familial, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sick sinus syndrome 1", "shortest_name_length": 4}
{"curie": "MONDO:0007598", "names": ["MCFD5", "FMFD V", "multiple coagulation Factor deficiency 5", "Multiple Coagulation Factor Deficiency V", "MULTIPLE COAGULATION FACTOR DEFICIENCY V", "factors VIII, 9 and Xi, combined deficiency of", "FACTORS VIII, IX AND XI, COMBINED DEFICIENCY OF", "Factors VIII, IX And XI, Combined Deficiency of", "factors VIII, IX and XI, combined deficiency of", "Familial Multiple Coagulation Factor Deficiency V", "familial multiple coagulation Factor deficiency 5", "FAMILIAL MULTIPLE COAGULATION FACTOR DEFICIENCY V"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "factors VIII, IX and XI, combined deficiency of", "shortest_name_length": 5}
{"curie": "UMLS:C5419811", "names": ["Liver Neuroendocrine Tumor G1", "Hepatic Neuroendocrine Tumor G1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liver Neuroendocrine Tumor G1", "shortest_name_length": 29}
{"curie": "UMLS:C1333043", "names": ["CMML-1", "Chronic Myelomonocytic Leukemia-1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic Myelomonocytic Leukemia-1", "shortest_name_length": 6}
{"curie": "UMLS:C1336092", "names": ["Stage 0 Lip Basal Cell Cancer", "Stage 0 Lip Basal Cell Carcinoma", "Lip Basal Cell Carcinoma in situ", "Basal Cell Carcinoma in situ of Lip", "Stage 0 Basal Cell Carcinoma of Lip", "Basal Cell Carcinoma in situ of the Lip", "Stage 0 Basal Cell Carcinoma of the Lip", "Stage 0 Lip Basal Cell Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Lip Basal Cell Carcinoma AJCC v6 and v7", "shortest_name_length": 29}
{"curie": "UMLS:C0751497", "names": ["Special Senses Disorder", "Special Senses Disorders", "Senses Disorder, Special", "Senses Disorders, Special"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Special Senses Disorders", "shortest_name_length": 23}
{"curie": "MONDO:0022897", "names": ["craniosynostosis exostoses nevus epibulbar dermoid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniosynostosis exostoses nevus epibulbar dermoid", "shortest_name_length": 50}
{"curie": "MONDO:0006208", "names": ["Fallopian Tube Serous Adenocarcinoma", "fallopian tube serous adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fallopian tube serous adenocarcinoma", "shortest_name_length": 36}
{"curie": "UMLS:C0027627", "names": ["Metastase", "secondary", "METASTASIS", "metastasis", "metastases", "Metastasis", "Metastases", "Metastasize", "secondaries", "metastasized", "METASTASES NOS", "Metastases NOS", "secondary tumor", "secondary tumors", "cancer secondary", "secondary cancer", "metastatic tumor", "tumor metastasis", "metastasis tumor", "metastatic tumors", "metastatic tumour", "metastatic cancer", "tumour metastasis", "cancers secondary", "metastatic disease", "spreading of tumor", "metastatic tumours", "Neoplasm Metastases", "metastatic neoplasm", "Neoplasm Metastasis", "Metastases, Neoplasm", "Tumor Cell Migration", "Metastasis, Neoplasm", "secondary malignancies", "spreading of cancer (tumor)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplasm Metastasis", "shortest_name_length": 9}
{"curie": "MONDO:0020043", "names": ["autosomal recessive congenital cerebellar ataxia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive congenital cerebellar ataxia", "shortest_name_length": 48}
{"curie": "UMLS:C1390461", "names": ["Bone contusion", "bone; contusion", "contusion; bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone contusion", "shortest_name_length": 14}
{"curie": "UMLS:C0278874", "names": ["Ependymoma", "adult ependymoma", "Adult Ependymoma", "ependymoma, adult", "adult CNS tumor, ependymoma", "CNS tumor, adult ependymoma", "CNS tumor, ependymoma, adult", "adult brain tumor, ependymoma", "brain tumor, adult ependymoma", "brain tumor, ependymoma, adult", "adult well-differentiated ependymoma", "Adult Well-Differentiated Ependymoma", "well-differentiated adult ependymoma", "Well-Differentiated Adult Ependymoma", "central nervous system tumor, ependymoma, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Ependymoma", "shortest_name_length": 10}
{"curie": "UMLS:C0259781", "names": ["nevus compound", "compound nevus", "Compound Nevus", "Compound nevus", "COMPOUND NEVUS", "Compound naevus", "compound naevus", "Naevus;compound", "Compound Nevus of Skin", "Compound nevus of skin", "Compound naevus of skin", "Dermal and epidermal nevus", "compound nevus (diagnosis)", "Compound Nevus of the Skin", "Dermal and epidermal naevus", "Compound nevus of skin (disorder)", "Compound nevus (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Compound nevus", "shortest_name_length": 14}
{"curie": "MONDO:0001624", "names": ["sphenoidal sinus -acute", "Sphenoidal sinus -acute", "acute sphenoid sinusitis", "sphenoid sinusitis, acute", "acute sphenoidal sinusitis", "Acute sphenoidal sinusitis", "Acute sinusitis, sphenoidal", "sinusitis; acute, sphenoidal", "sinusitis; sphenoidal, acute", "Acute sphenoidal sinusitis (disorder)", "acute sphenoidal sinusitis (diagnosis)", "Acute sphenoidal sinusitis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute sphenoidal sinusitis", "shortest_name_length": 23}
{"curie": "MONDO:0016782", "names": ["paternal 14q32.2 hypomethylation syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paternal 14q32.2 hypomethylation syndrome", "shortest_name_length": 41}
{"curie": "MONDO:0012643", "names": ["SPG32", "spastic paraplegia 32", "hereditary spastic paraplegia 32", "hereditary spastic paraplegia type 32", "autosomal recessive spastic paraplegia 32", "Spastic Paraplegia 32, Autosomal Recessive", "spastic paraplegia 32, autosomal recessive", "SPASTIC PARAPLEGIA 32, AUTOSOMAL RECESSIVE", "Autosomal recessive spastic paraplegia type 32", "autosomal recessive spastic paraplegia type 32", "familial spastic paraplegia autosomal recessive type 32", "Autosomal recessive spastic paraplegia type 32 (disorder)", "Autosomal recessive spastic paraplegia type 32 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 32", "shortest_name_length": 5}
{"curie": "MONDO:0010058", "names": ["SPSMA", "Scapuloperoneal neuronopathy", "SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY", "Scapuloperoneal spinal muscular atrophy", "Scapuloperoneal Spinal Muscular Atrophy", "SPINAL MUSCULAR ATROPHY, SCAPULOPERONEAL", "spinal muscular atrophy, scapuloperoneal", "Spinal Muscular Atrophy, Scapuloperoneal", "Scapuloperoneal form spinal muscular atrophy", "Spinal Muscular Atrophy, Scapuloperoneal Form", "atrophy; muscle, spinal, scapuloperoneal form", "muscle; atrophy, spinal, scapuloperoneal form", "Scapuloperoneal Form of Spinal Muscular Atrophy", "Scapuloperoneal spinal muscular atrophy (disorder)", "Neurogenic scapuloperoneal amyotrophy, New England type", "AMYOTROPHY, NEUROGENIC SCAPULOPERONEAL, NEW ENGLAND TYPE", "Amyotrophy, Neurogenic Scapuloperoneal, New England Type", "scapuloperoneal spinal muscular atrophy, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scapuloperoneal spinal muscular atrophy, autosomal recessive", "shortest_name_length": 5}
{"curie": "UMLS:C5420307", "names": ["Unresectable Pleural Epithelioid Mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Pleural Epithelioid Mesothelioma", "shortest_name_length": 45}
{"curie": "MONDO:0044202", "names": ["EKD", "familial PKD", "episodic kinesigenic dyskinesia", "paroxysmal kinesigenic choreathetosis", "familial paroxysmal kinesigenic dyskinesia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "episodic kinesigenic dyskinesia", "shortest_name_length": 3}
{"curie": "UMLS:C0265329", "names": ["solomon syndrome", "organoid nevus syndrome", "Feuerstein Mims Syndrome", "epidermal nevus syndrome", "Feuerstein-Mims Syndrome", "Schimmelpenning Syndrome", "nevus sebaceous syndrome", "feuerstein-mims syndrome", "sebaceous nevus syndrome", "Epidermal nevus syndrome", "Epidermal naevus syndrome", "Syndrome, Schimmelpenning", "epidermal naevus syndrome", "nevus sebaceous jadassohn", "Syndrome, Feuerstein-Mims", "Organoid Nevus Phakomatosis", "Organoid Nevus Phakomatoses", "Phakomatoses, Organoid Nevus", "jadassohn nevus phakomatosis", "Nevus Phakomatosis, Organoid", "Phakomatosis, Organoid Nevus", "nevus sebaceous of jadassohn", "sebaceous nevus of jadassohn", "Nevus Phakomatoses, Organoid", "linear sebaceous nevus syndrome", "linear nevus sebaceous syndrome", "linear verrucous epidermal nevus", "Schimmelpenning-Feuerstein-Mims syndrome", "Schimmelpenning-Feuerstein-Mims Syndrome", "Schimmelpenning Feuerstein Mims Syndrome", "Syndrome, Schimmelpenning-Feuerstein-Mims"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Organoid Nevus Phakomatosis", "shortest_name_length": 16}
{"curie": "UMLS:C5671041", "names": ["Stage III Cervical Cancer FIGO 2009", "Stage III Cervical Carcinoma FIGO 2009"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Cervical Cancer FIGO 2009", "shortest_name_length": 35}
{"curie": "MONDO:0018706", "names": ["syndromic sensorineural deafness due to COXPD", "syndromic sensorineural hearing loss due to COXPD", "syndromic sensorineural deafness due to combined oxidative phosphorylation defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic sensorineural deafness due to combined oxidative phosphorylation defect", "shortest_name_length": 45}
{"curie": "MONDO:0011734", "names": ["Cardioneuromyopathy with hyaline masses and nemaline rods", "CARDIONEUROMYOPATHY WITH HYALINE MASSES AND NEMALINE RODS", "Cardioneuromyopathy with Hyaline Masses and Nemaline Rods"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardioneuromyopathy with hyaline masses and nemaline rods", "shortest_name_length": 57}
{"curie": "UMLS:C4761241", "names": ["Partial neonatal hearing loss", "Partial Neonatal Hearing loss", "Partial Neonatal Hearing Loss"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Partial neonatal hearing loss", "shortest_name_length": 29}
{"curie": "MONDO:0001887", "names": ["Allen-Masters", "Masters-Allen", "allen master syndrome", "Allen-Masters syndrome", "masters-allen syndrome", "allen-masters syndrome", "Masters-Allen syndrome", "allen masters syndrome", "laceration of broad ligament", "Broad ligament laceration syndrome", "broad ligament; laceration syndrome", "syndrome; broad ligament laceration", "laceration; syndrome, broad ligament", "Ligamentum latum laceration syndrome", "laceration of broad ligament (diagnosis)", "Broad ligament laceration syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Allen-Masters syndrome", "shortest_name_length": 13}
{"curie": "UMLS:C1516065", "names": ["Astler-Coller B3 Colon Carcinoma", "Astler-Coller B3 Colonic Carcinoma", "Astler-Coller B3 Carcinoma of Colon", "Astler-Coller B3 Carcinoma of the Colon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Astler-Coller B3 Colon Carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0017462", "names": ["congenital pseudoarthrosis tibia", "Congenital Pseudarthrosis of Tibia", "congenital pseudarthrosis of tibia", "Congenital pseudarthrosis of tibia", "Congenital pseudoarthrosis of tibia", "congenital pseudarthrosis of the tibia", "Congenital pseudarthrosis of the tibia", "Congenital pseudoarthrosis of the tibia", "congenital pseudoarthrosis of the tibia", "Congenital pseudoarthrosis of tibia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital pseudoarthrosis of the tibia", "shortest_name_length": 32}
{"curie": "UMLS:C2986679", "names": ["Stage III Non-Hodgkin Lymphoma", "Stage III Childhood Non-Hodgkin Lymphoma", "stage III childhood non-Hodgkin lymphoma", "Ann Arbor Stage III Childhood Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Childhood Non-Hodgkin Lymphoma", "shortest_name_length": 30}
{"curie": "MONDO:0016573", "names": ["AFLP", "fatty liver pregnancy", "fatty liver of pregnancy", "Fatty liver of pregnancy", "acute fatty liver pregnancy", "Acute fatty liver of pregnancy", "acute fatty liver of pregnancy", "acute fatty liver, gestational", "FATTY LIVER OF PREGNANCY ACUTE", "Acute fatty liver, gestational", "AFLP (acute fatty liver of pregnancy)", "AFLP - acute fatty liver of pregnancy", "AFLP - Acute fatty liver of pregnancy", "Acute fatty liver of pregnancy (disorder)", "pregnancy complications: acute fatty liver", "Acute fatty liver of pregnancy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute fatty liver of pregnancy", "shortest_name_length": 4}
{"curie": "UMLS:C1708650", "names": ["Laryngeal Basaloid Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laryngeal Basaloid Carcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0008361", "names": ["radius, aplasia of, with cleft lip/palate", "RADIUS, APLASIA OF, WITH CLEFT LIP/PALATE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radius, aplasia of, with cleft lip/palate", "shortest_name_length": 41}
{"curie": "MONDO:0004876", "names": ["Myocardial stunning", "myocardial stunning", "Myocardial Stunning", "Stunning, Myocardial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myocardial stunning", "shortest_name_length": 19}
{"curie": "MONDO:0015024", "names": ["ECTD12", "ectodermal dysplasia 12", "KDF1 ectodermal dysplasia syndrome", "ectodermal dysplasia syndrome caused by mutation in KDF1", "ECTODERMAL DYSPLASIA 12, HYPOHIDROTIC/HAIR/TOOTH/NAIL TYPE", "ectodermal dysplasia 12, hypohidrotic/hair/tooth/nail type", "ectodermal dysplasia 12, hypohidrotic/hair/Tooth/nail type", "ectodermal dysplasia 12, hypohidrotic/hair/tooth/nail type; ECTD12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia 12, hypohidrotic/hair/tooth/nail type", "shortest_name_length": 6}
{"curie": "MONDO:0001080", "names": ["Gonococcal cervicitis", "acute gonorrhea of cervix", "Acute gonorrhea of cervix", "CERVICITIS GONOCOCCAL ACUTE", "acute gonococcal cervicitis", "Gonococcal cervicitis acute", "Cervicitis gonococcal acute", "cervicitis gonococcus acute", "Acute gonococcal cervicitis", "gonococcal cervicitis, acute", "Gonococcal cervicitis (acute)", "gonococcal cervicitis (acute)", "Acute gonococcal cervicitis (disorder)", "Acute gonococcal cervicitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute gonococcal cervicitis", "shortest_name_length": 21}
{"curie": "UMLS:C2987190", "names": ["Pancreatic Intraductal Tubulopapillary Neoplasm with an Associated Invasive Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Intraductal Tubulopapillary Neoplasm with an Associated Invasive Carcinoma", "shortest_name_length": 85}
{"curie": "OMIM:615082", "names": ["C3HEX, ABILITY TO SMELL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 23}
{"curie": "UMLS:C0342778", "names": ["Complex III deficiency", "complex deficiency iii", "complex iii deficiency", "Ubiquinone dehydrogenase", "Ubiquinone dehydrogenase deficiency", "Ubiquinone dehydrogenase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ubiquinone dehydrogenase deficiency", "shortest_name_length": 22}
{"curie": "MONDO:0013897", "names": ["LDS4", "Loeys-Dietz syndrome 4", "LOEYS-DIETZ SYNDROME 4", "TGFB2 Loeys-Dietz syndrome", "Loeys-Dietz syndrome type 4", "Loeys-Dietz syndrome type 4 (diagnosis)", "Loeys-Dietz syndrome caused by mutation in TGFB2", "ANEURYSM, AORTIC AND CEREBRAL, WITH ARTERIAL TORTUOSITY AND SKELETAL MANIFESTATIONS", "Aneurysm, aortic and cerebral, with arterial tortuosity and skeletal manifestations", "aneurysm, aortic and cerebral, with arterial tortuosity and skeletal manifestations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Loeys-Dietz syndrome 4", "shortest_name_length": 4}
{"curie": "MONDO:0003310", "names": ["mönckeberg's", "Monckeberg Sclerosis", "Mönckeberg Sclerosis", "Mönckebergs Sclerosis", "Monckebergs Sclerosis", "Monckeberg's Sclerosis", "Monckeberg's sclerosis", "Mönckeberg's Sclerosis", "Sclerosis, Mönckeberg's", "mönckeberg's; sclerosis", "Sclerosis, Monckeberg's", "sclerosis; mönckeberg's", "Medial Calcific Scleroses", "medial calcific sclerosis", "Medial Calcific Sclerosis", "mönckeberg's; degeneration", "Calcific Sclerosis, Medial", "Scleroses, Medial Calcific", "Calcific Scleroses, Medial", "Sclerosis, Medial Calcific", "degeneration; mönckeberg's", "Monckeberg Arteriosclerosis", "Mönckeberg Arteriosclerosis", "mönckeberg's; calcification", "Monckeberg arteriosclerosis", "Monckeberg medial sclerosis", "calcification; mönckeberg's", "Mönckeberg arteriosclerosis", "Monckeberg's medial sclerosis", "Monckeberg's arteriosclerosis", "Arteriosclerosis, Monckeberg's", "mönckeberg's; arteriosclerosis", "arteriosclerosis; mönckeberg's", "Monckeberg's medial calcinosis", "Mönckeberg's (medial) sclerosis", "Arteriosclerosis Monckeberg-type", "Arteriosclerosis Moenckeberg-type", "Monckeberg's descending sclerosis", "ARTERIOSCLEROSIS MOENCKEBERG-TYPE", "Mönckeberg Medial Calcific Sclerosis", "Monckeberg Medial Calcific Sclerosis", "Sclerosis, Mönckeberg Medial Calcific", "Sclerosis, Monckeberg Medial Calcific", "Mönckeberg's Medial Calcific Sclerosis", "Monckeberg's Medial Calcific Sclerosis", "Monckeberg's medial sclerosis (disorder)", "Monckeberg's arteriosclerosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Monckeberg arteriosclerosis", "shortest_name_length": 12}
{"curie": "UMLS:C0341512", "names": ["hematoma retroperitoneal", "Retroperitoneal hematoma", "retroperitoneal hematoma", "RETROPERITONEAL HEMATOMA", "Retroperitoneal haematoma", "hematoma; retroperitoneal", "hematomas retroperitoneal", "retroperitoneal; hematoma", "Retroperitoneal hematoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retroperitoneal hematoma", "shortest_name_length": 24}
{"curie": "UMLS:C4525733", "names": ["Posterior Subcapsular Cataract Grade 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Posterior Subcapsular Cataract Grade 3", "shortest_name_length": 38}
{"curie": "MONDO:0000827", "names": ["SALMONELLA", "Salmonella", "salmonella", "Salmonellosis", "Salmonelloses", "SALMONELLOSIS", "salmonelloses", "salmonellosis", "Salmonella Infection", "Salmonella infection", "SALMONELLA INFECTION", "salmonella infection", "Salmonella infections", "infection; Salmonella", "Salmonella Infections", "salmonella infections", "Infection, Salmonella", "Infections, Salmonella", "infections, Salmonella", "Salmonella infection NOS", "rare form of salmonellosis", "Salmonella infection (disorder)", "Salmonella infection (diagnosis)", "Salmonella infection, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "salmonellosis", "shortest_name_length": 10}
{"curie": "MONDO:0021117", "names": ["lung", "Lung Tumor", "Lung tumor", "LUNG TUMOR", "lung tumor", "Lung tumour", "lung tumors", "Lung cancer", "lung tumour", "lung tumours", "tumor of lung", "Lung neoplasm", "Tumor of lung", "Lungs--Tumors", "Tumor of Lung", "lung neoplasm", "Lung Neoplasm", "neoplasm, lung", "lung neoplasms", "Lung Neoplasms", "tumour of lung", "Tumour of lung", "Neoplasm, Lung", "neoplasms, lung", "Neoplasms, Lung", "neoplasm of lung", "Neoplasm of lung", "Neoplasm of Lung", "Tumor of the Lung", "Lung neoplasm NOS", "tumor of the lung", "Pulmonary Neoplasm", "pulmonary neoplasm", "Neoplasm, Pulmonary", "Pulmonary Neoplasms", "pulmonary neoplasms", "neoplasm, pulmonary", "Pulmonary neoplasia", "Neoplasm of the lung", "neoplasm of the lung", "neoplasms, pulmonary", "Neoplasm of the Lung", "Neoplasms, Pulmonary", "lung neoplasm (disease)", "Neoplasm of lung (disorder)", "neoplasm of lung (diagnosis)", "pulmonary neoplasms (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung neoplasm", "shortest_name_length": 4}
{"curie": "UMLS:C0855076", "names": ["Hodgkin's disease lymphocyte predominance type stage III", "Stage III Hodgkin's Disease Lymphocyte Predominance Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's disease lymphocyte predominance type stage III", "shortest_name_length": 56}
{"curie": "MONDO:0100403", "names": ["AML, del(17p)", "AML, loss of chromosome 17p", "acute myeloid leukemia, loss of chromosome 17p"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, loss of chromosome 17p", "shortest_name_length": 13}
{"curie": "UMLS:C4727787", "names": ["Metastatic Triple-Negative Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Triple-Negative Breast Carcinoma", "shortest_name_length": 43}
{"curie": "UMLS:C0029233", "names": ["PERSONALITY DISORDER ORGANIC", "Organic personality disorder", "organic personality syndrome", "Organic Personality Syndrome", "Personality syndrome organic", "Organic personality syndrome", "organic personality disorder", "disorders organic personality", "personality disorder; organic", "organic; personality disorder", "organic; disorder, personality", "Organic personality disorder, NOS", "Organic personality disorder (disorder)", "organic personality disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Organic personality disorder", "shortest_name_length": 28}
{"curie": "EFO:0009087", "names": ["non-typhoidal Salmonella bacteremia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-typhoidal Salmonella bacteremia", "shortest_name_length": 35}
{"curie": "MONDO:0007382", "names": ["RAMOS-ARROYO SYNDROME", "Ramos Arroyo syndrome", "Ramos Arroyo Syndrome", "Ramos-Arroyo syndrome", "Ramos Arroyo Clark syndrome", "Ramos Arroyo syndrome (disorder)", "Ramos Arroyo syndrome (diagnosis)", "corneal anesthesia-deafness-intellectual disability syndrome", "Corneal anesthesia-deafness-intellectual disability syndrome", "Corneal anesthesia, deafness, intellectual disability syndrome", "Corneal anaesthesia, deafness, intellectual disability syndrome", "Corneal anesthesia-hearing loss-intellectual disability syndrome", "congenital corneal anesthesia with retinal abnormalities, deafness, unusual facies, persistent ductus arteriosus, and mental retardation", "corneal hypesthesia with retinal abnormalities, sensorineural deafness, unusual facies, persistent ductus arteriosus, and mental retardation", "CORNEAL HYPESTHESIA WITH RETINAL ABNORMALITIES, SENSORINEURAL DEAFNESS, UNUSUAL FACIES, PERSISTENT DUCTUS ARTERIOSUS, AND MENTAL RETARDATION", "congenital corneal anesthesia with retinal abnormalities, deafness, unusual facies, persistent ductus arteriosus, and intellectual disability", "corneal hypesthesia with retinal abnormalities, sensorineural deafness, unusual facies, persistent ductus arteriosus, and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ramos-Arroyo syndrome", "shortest_name_length": 21}
{"curie": "MONDO:0001452", "names": ["Pseudoretinitis pigmentosa", "pseudoretinitis pigmentosa", "pseudoretinitis pigmentosum", "pseudo-retinitis pigmentosa", "Secondary pigmentary degeneration", "pseudoretinitis pigmentosum (diagnosis)", "secondary pigmentary retinal degeneration", "Secondary pigmentary retinal degeneration", "secondary pigmentary degeneration of retina", "Secondary pigmentary degeneration of retina", "Secondary pigmentary retinal degeneration (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudoretinitis pigmentosa", "shortest_name_length": 26}
{"curie": "MONDO:0022874", "names": ["corpus callosum dysgenesis hypopituitarism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corpus callosum dysgenesis hypopituitarism", "shortest_name_length": 42}
{"curie": "UMLS:C4331987", "names": ["Stage IVA Oropharyngeal (p16-Negative) Throat Cancer", "Stage IVA Oropharyngeal (p16-Negative) Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Oropharyngeal (p16-Negative) Carcinoma AJCC v8", "shortest_name_length": 52}
{"curie": "MONDO:0012434", "names": ["ARVD10", "ARVC10", "arrhythmogenic right ventricular dysplasia 10", "arrhythmogenic right ventricular dysplasia type 10", "arrhythmogenic right ventricular cardiomyopathy 10", "Arrhythmogenic Right Ventricular Cardiomyopathy 10", "ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 10", "DSG2 arrhythmogenic right ventricular cardiomyopathy", "familial arrhythmogenic right ventricular dysplasia 10", "Familial Arrhythmogenic Right Ventricular Dysplasia 10", "arrhythmogenic right ventricular dysplasia, familial, 10", "Arrhythmogenic Right Ventricular Dysplasia, Familial, 10", "ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10", "arrhythmogenic right ventricular dysplasia, familial, type 10", "arrhythmogenic right ventricular cardiomyopathy caused by mutation in DSG2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arrhythmogenic right ventricular dysplasia 10", "shortest_name_length": 6}
{"curie": "MONDO:0007892", "names": ["LMHD", "Lenz-Majewski syndrome", "LENZ-MAJEWSKI SYNDROME", "Lenz-Majewski dysplasia", "LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM", "Lenz-Majewski Hyperostotic Dwarfism", "Lenz Majewski hyperostotic dwarfism", "Lenz-Majewski hyperostotic dwarfism", "Lenz-Majewski hyperostosis syndrome", "Lenz-Majewski hyperostotic dysplasia", "hyperostotic dwarfism Lenz-Majewski type", "Lenz-Majewski hyperostosis syndrome (disorder)", "multiple congenital anomalies, mental retardation and progressive skeletal sclerosis", "Multiple congenital anomalies, mental retardation, and progressive skeletal sclerosis", "multiple congenital anomalies, intellectual disability and progressive skeletal sclerosis", "Delayed closure of fontanel, proximal symphalangism, prominent cutaneous veins,mental retardation, and progressive skeletal sclerosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lenz-Majewski hyperostotic dwarfism", "shortest_name_length": 4}
{"curie": "MONDO:0006138", "names": ["cervical neuroendocrine tumor", "Cervical Large Cell Neuroendocrine Carcinoma", "cervical large cell neuroendocrine carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical large cell neuroendocrine carcinoma", "shortest_name_length": 29}
{"curie": "UMLS:C0948702", "names": ["Upper respiratory fungal infection", "Upper respiratory fungal infection NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Upper respiratory fungal infection", "shortest_name_length": 34}
{"curie": "MONDO:0021233", "names": ["Ear Tumor", "Ear tumor", "ear tumor", "tumor of Ear", "ear neoplasm", "Ear Neoplasm", "tumor of ear", "Tumor of Ear", "Ear Neoplasms", "Ear neoplasms", "Neoplasm of Ear", "neoplasm of Ear", "neoplasm of ear", "tumor of the Ear", "Tumor of the Ear", "neoplasm of the Ear", "Neoplasm of the Ear", "ear neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ear neoplasm", "shortest_name_length": 9}
{"curie": "MONDO:0100395", "names": ["AML, t(5;11)(q35;p15)", "AML with t(5;11)(q35;p15); NUP98-NSD1", "acute myeloid leukemia, t(5;11)(q35;p15)", "Acute Myeloid Leukemia with t(5;11)(q35;p15); NUP98-NSD1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, t(5;11)(q35;p15)", "shortest_name_length": 21}
{"curie": "UMLS:C3272438", "names": ["Ampullary Flat Intraepithelial Neoplasia, High Grade", "Ampullary Flat Intraepithelial Neoplasia (Dysplasia), High Grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ampullary Flat Intraepithelial Neoplasia, High Grade", "shortest_name_length": 52}
{"curie": "MONDO:0014854", "names": ["DFNA66", "autosomal dominant deafness 66", "deafness, autosomal dominant 66", "DEAFNESS, AUTOSOMAL DOMINANT 66", "deafness, autosomal dominant type 66", "autosomal dominant nonsyndromic deafness 66", "CD164 autosomal dominant nonsyndromic deafness", "autosomal dominant nonsyndromic hearing loss 66", "autosomal dominant nonsyndromic deafness type 66", "autosomal dominant nonsyndromic deafness caused by mutation in CD164"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 66", "shortest_name_length": 6}
{"curie": "MONDO:0019784", "names": ["Del(12)(q14)", "Deletion 12q14", "deletion 12q14", "monosomy 12q14", "Monosomy 12q14", "12q14 microdeletion syndrome", "12q14 microdeletion syndrome (disorder)", "12q14 microdeletion syndrome (diagnosis)", "Osteopoikilosis-short stature-intellectual disability syndrome", "osteopoikilosis-short stature-intellectual disability syndrome", "Osteopoikilosis with short stature and intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "12q14 microdeletion syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0001294", "names": ["Horner", "Bernard-Horner", "HORNER SYNDROME", "Horner syndrome", "Horner Syndrome", "horner syndrome", "horners syndrome", "Syndrome, Horner", "Bernard Syndrome", "Horners Syndrome", "Bernard Syndromes", "Bernards Syndrome", "Syndrome, Bernard", "HORNER'S SYNDROME", "Horner's syndrome", "horner's syndrome", "Horner's Syndrome", "Bernard's syndrome", "Syndromes, Bernard", "Syndrome, Horner's", "Bernard's Syndrome", "Syndrome, Bernard's", "Horner syndrome pupil", "Claude Bernard-Horner", "Oculosympathetic palsy", "Horner Syndrome, Pupil", "oculosympathetic palsy", "Horners Syndrome, Pupil", "Pupil Horner's Syndrome", "Bernard-Horner syndrome", "bernard horner syndrome", "Horner's syndrome pupil", "Bernard Horner syndrome", "Syndrome, Pupil Horner's", "Horner's Syndrome, Pupil", "Oculosympathetic Syndrome", "Bernard(-Horner) syndrome", "Oculosympathetic syndrome", "Oculosympathetic Syndromes", "Syndrome, Oculosympathetic", "Syndromes, Oculosympathetic", "Miosis innervational defect", "sympathetic ophthalmoplegia", "OPHTHALMOPLEGIA, SYMPATHETIC", "Miosis, Innervational Defect", "Horner's syndrome (diagnosis)", "Cervical sympathetic syndrome", "Cervical sympathetic paralysis", "CLAUDE BERNARD-HORNER SYNDROME", "Claude Bernard Horner Syndrome", "claude bernard-horner syndrome", "Claude Bernard-Horner Syndrome", "cervical sympathetic paralysis", "paralysis; cervical sympathetic", "Syndrome, Claude Bernard-Horner", "sympathetic; paralysis, cervical", "paralysis; sympathetic, cervical", "Horner's syndrome pupil (disorder)", "Sympathetic Ocular Ophthalmoplegia", "Sympathetic Ocular-Ophthalmoplegia", "Ocular Ophthalmoplegia, Sympathetic", "Ophthalmoplegia, Sympathetic Ocular", "Ocular-Ophthalmoplegia, Sympathetic", "Sympathetic Ocular-Ophthalmoplegias", "Sympathetic Ocular Ophthalmoplegias", "Ocular Ophthalmoplegias, Sympathetic", "Ophthalmoplegias, Sympathetic Ocular", "Ocular-Ophthalmoplegias, Sympathetic", "Paralysis of cervical sympathetic trunk", "CERVICAL SYMPATHETIC PARALYSIS SYNDROME", "syndrome; cervical, sympathetic paralysis", "sympathetic; syndrome, cervical paralysis", "cervical; syndrome, sympathetic paralysis", "syndrome; sympathetic, cervical paralysis", "cervical; sympathetic paralysis (syndrome)", "cervical sympathetic paralysis (diagnosis)", "sympathetic; cervical paralysis (syndrome)", "cervical; paralysis, sympathetic (syndrome)", "sympathetic; paralysis, cervical (syndrome)", "Paralysis of cervical sympathetic trunk (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Horner syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0006496", "names": ["palsy", "Palsy", "Plegia", "plegia", "plegias", "Plegias", "Palsies", "palsies", "palsied", "paralyse", "paralysis", "Paralysed", "PARALYSIS", "Paralysis", "Paralyzed", "paralyses", "Paralyses", "Paralysis NOS", "Paralysis, NOS", "Inability to move", "Paralytic Syndrome", "Paralysis (finding)", "Paralysis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "palsy", "shortest_name_length": 5}
{"curie": "UMLS:C5420820", "names": ["Metastatic Malignant Neoplasm in the Uvea"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Malignant Neoplasm in the Uvea", "shortest_name_length": 41}
{"curie": "UMLS:C2347755", "names": ["Supratentorial Embryonal Tumor, NOS", "Adult Supratentorial Embryonal Tumor, NOS", "Adult Supratentorial Primitive Neuroectodermal Tumor", "adult supratentorial primitive neuroectodermal tumor", "adult supratentorial primitive neuroectodermal tumor (PNET)", "supratentorial primitive neuroectodermal tumor (PNET), adult", "Adult Supratentorial Embryonal Tumor, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Supratentorial Embryonal Tumor, Not Otherwise Specified", "shortest_name_length": 35}
{"curie": "MONDO:0021923", "names": ["Arroyo Garcia Cimadevilla syndrome", "bilateral anophthalmia, esophageal atresia, and right cryptorchidism", "Bilateral anophthalmia, esophageal atresia, and right cryptorchidism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arroyo Garcia Cimadevilla syndrome", "shortest_name_length": 34}
{"curie": "MONDO:0016966", "names": ["trisomy 16q", "16q trisomy", "Trisomy 16q", "Duplication 16q", "16q duplication", "partial trisomy 16q", "Chromosome 16, trisomy 16q", "chromosome 16q duplication", "partial trisomy of chromosome 16q", "partial duplication of chromosome 16q", "partial trisomy of the long arm of chromosome 16", "partial duplication of the long arm of chromosome 16", "partial trisomy of the long arm of chromosome type 16"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial trisomy of the long arm of chromosome 16", "shortest_name_length": 11}
{"curie": "MONDO:0022504", "names": ["arthrogryposis spinal muscular atrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis spinal muscular atrophy", "shortest_name_length": 38}
{"curie": "OMIM:111300", "names": [], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"]}
{"curie": "UMLS:C0270381", "names": ["Subchronic schizophrenia", "subchronic schizophrenia", "Subchronic Schizophrenia", "Subchronic schizophrenia, NOS", "Subchronic schizophrenia (disorder)", "subchronic schizophrenia (diagnosis)", "Unspecified schizophrenia, subchronic", "Unspecified schizophrenia, subchronic state"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subchronic schizophrenia", "shortest_name_length": 24}
{"curie": "MONDO:0003158", "names": ["Myoepithelial carcinoma", "Myoepithelial Carcinoma", "myoepithelial carcinoma", "Malignant Myoepithelioma", "myoepithelioma carcinoma", "malignant myoepithelioma", "Malignant myoepithelioma", "MYOEPITHELIOMA, MALIGNANT", "myoepithelioma, malignant", "Infiltrating myoepithelioma", "soft tissue myoepithelial carcinoma", "malignant myoepithelioma (diagnosis)", "Malignant myoepithelioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant myoepithelioma", "shortest_name_length": 23}
{"curie": "UMLS:C0740391", "names": ["a.cerebri media; occlusion", "Middle cerebral artery occlusion", "middle cerebral artery occlusion", "cerebral artery occlusion middle", "Middle Cerebral Artery Occlusion", "occlusion; middle cerebral artery", "Occlusion, Middle Cerebral Artery", "Middle cerebral artery occlusion (disorder)", "middle cerebral artery occlusion (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Middle Cerebral Artery Occlusion", "shortest_name_length": 26}
{"curie": "UMLS:C0852964", "names": ["Blocked;shunt", "blocked shunt", "blocked shunts", "Shunt occlusion", "shunt occlusion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Shunt occlusion", "shortest_name_length": 13}
{"curie": "UMLS:C0278810", "names": ["localized extrahepatic bile duct cancer", "Localized Extrahepatic Bile Duct Cancer", "bile duct cancer, localized extrahepatic", "extrahepatic bile duct cancer, localized", "Localized Extrahepatic Bile Duct Carcinoma", "Localized Cancer of Extrahepatic Bile Duct", "Localized Cancer of the Extrahepatic Bile Duct"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized Extrahepatic Bile Duct Carcinoma", "shortest_name_length": 39}
{"curie": "UMLS:C0861220", "names": ["Stage III Centroblastic Lymphoma", "Centroblastic lymphoma stage III", "Ann Arbor Stage III Centroblastic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Centroblastic lymphoma stage III", "shortest_name_length": 32}
{"curie": "MONDO:0010636", "names": ["Spastic Paraplegia-Kallmann Syndrome", "SPASTIC PARAPLEGIA-KALLMANN SYNDROME", "spastic paraplegia-Kallmann syndrome", "Spastic paraplegia with Kallmann syndrome", "Kallmann syndrome with spastic paraplegia", "KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA", "Familial spastic paraplegia with Kallmann's syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kallmann syndrome with spastic paraplegia", "shortest_name_length": 36}
{"curie": "MONDO:0008407", "names": ["SCPNK", "KAESER SYNDROME", "Kaeser Syndrome", "Kaeser syndrome", "stark-Kaeser syndrome", "Stark-Kaeser syndrome", "Stark Kaeser syndrome", "Stark-Kaeser Syndrome", "STARK-KAESER SYNDROME", "scapuloperoneal syndrome type Kaeser", "neurogenic scapuloperoneal syndrome Kaeser type", "Neurogenic scapuloperoneal syndrome Kaeser type", "neurogenic scapuloperoneal syndrome, Kaeser type", "Neurogenic scapuloperoneal syndrome, Kaeser type", "Scapuloperoneal Syndrome, Neurogenic, Kaeser Type", "scapuloperoneal syndrome, neurogenic, Kaeser type", "SCAPULOPERONEAL SYNDROME, NEUROGENIC, KAESER TYPE", "scapuloperoneal syndrome, neurogenic type, of Kaeser", "SCAPULOPERONEAL SYNDROME, NEUROGENIC TYPE, OF KAESER", "Neurogenic scapuloperoneal syndrome Kaeser type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurogenic scapuloperoneal syndrome, Kaeser type", "shortest_name_length": 5}
{"curie": "UMLS:C0751592", "names": ["Benign Infratentorial Tumor", "Benign Infratentorial Neoplasm", "Benign Infratentorial Neoplasms", "Neoplasm, Benign Infratentorial", "Infratentorial Neoplasm, Benign", "Infratentorial Neoplasms, Benign"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Infratentorial Neoplasms", "shortest_name_length": 27}
{"curie": "MONDO:0024857", "names": ["Immature Extragonadal Teratoma", "immature extragonadal teratoma", "malignant extragonadal teratoma", "extragonadal primary malignant teratoma", "primary malignant extragonadal teratoma", "Extragonadal primary malignant teratoma", "Extragonadal primary malignant teratoma NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immature extragonadal teratoma", "shortest_name_length": 30}
{"curie": "MONDO:0002612", "names": ["frontal lobe epilepsy", "Frontal Lobe Epilepsy", "epilepsy frontal lobe", "Frontal lobe epilepsy", "Epilepsy, Frontal Lobe", "Frontal Lobe Epilepsies", "epilepsy of frontal lobe", "Frontal lobe epilepsy (disorder)", "frontal lobe epilepsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontal lobe epilepsy", "shortest_name_length": 21}
{"curie": "UMLS:C0920038", "names": ["n.medianus; paralysis", "Median Nerve Paralysis", "Paralysis median nerve", "paralysis; median nerve"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paralysis median nerve", "shortest_name_length": 21}
{"curie": "UMLS:C5556775", "names": ["Optic Nerve Palsy", "Cranial nerve palsy II", "Cranial Nerve II Palsy", "Second Cranial Nerve Palsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cranial Nerve II Palsy", "shortest_name_length": 17}
{"curie": "UMLS:C1334035", "names": ["Hodgkin-Like Adult T-Cell Leukemia/Lymphoma", "Hodgkin-Like Adult T-Cell Lymphoma/Leukemia", "Hodgkin's-Like Adult T-Cell Lymphoma/Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin-Like Adult T-Cell Leukemia/Lymphoma", "shortest_name_length": 43}
{"curie": "UMLS:C4525345", "names": ["IIIC", "Stage IIIC Hilar Cholangiocarcinoma", "Stage IIIC Hilar Cholangiocarcinoma AJCC v8", "Stage IIIC Perihilar Cholangiocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Hilar Cholangiocarcinoma AJCC v8", "shortest_name_length": 4}
{"curie": "MONDO:0003275", "names": ["middle ear cancer", "cancer of middle ear", "neoplasm of middle ear", "tumor of the middle ear", "Malignant Middle Ear Tumor", "malignant middle Ear tumor", "malignant tumor of middle Ear", "Malignant tumor of middle ear", "Malignant middle ear neoplasm", "Malignant Tumor of Middle Ear", "Malignant Middle Ear Neoplasm", "malignant middle ear neoplasm", "Malignant tumour of middle ear", "Malignant Neoplasm of Middle Ear", "malignant neoplasm of middle ear", "Malignant neoplasm of middle ear", "Malignant middle ear neoplasm NOS", "malignant tumor of the middle Ear", "Malignant Tumor of the Middle Ear", "malignant neoplasm of the middle Ear", "Malignant Neoplasm of the Middle Ear", "Malignant tumor of middle ear (disorder)", "auditory neoplasm malignant of middle ear", "malignant neoplasm of middle ear (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "middle ear cancer", "shortest_name_length": 17}
{"curie": "UMLS:C2063869", "names": ["Pancreatic Mature Teratoma", "mature pancreatic teratoma", "Mature Pancreatic Teratoma", "benign mature teratoma of pancreas", "benign mature teratoma of pancreas (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign mature teratoma of pancreas", "shortest_name_length": 26}
{"curie": "UMLS:C0752105", "names": ["Juvenile Parkinsonism", "juvenile parkinsonism", "Parkinsonism, Juvenile", "Juvenile Parkinsonisms", "Parkinsonisms, Juvenile", "Juvenile Parkinson disease", "juvenile paralysis agitans", "Juvenile Parkinson Disease", "disease juvenile parkinson", "Paralysis agitans, juvenile", "Parkinson Disease, Juvenile", "disease juvenile parkinsons", "parkinson's disease juvenile", "juvenile parkinson's disease", "Juvenile Parkinson's disease", "juvenile paralysis agitans (diagnosis)", "Juvenile Parkinson's disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parkinsonism, Juvenile", "shortest_name_length": 21}
{"curie": "MONDO:0002979", "names": ["Papillary Squamous Carcinoma", "papillary squamous carcinoma", "Papillary epidermoid carcinoma", "Papillary Epidermoid Carcinoma", "papillary epidermoid carcinoma", "Papillary squamous cell carcinoma", "Papillary Squamous Cell Carcinoma", "papillary squamous cell carcinoma", "papillary epidermoid cell carcinoma", "Papillary Epidermoid Cell Carcinoma", "papillary squamous cell carcinoma (diagnosis)", "Papillary squamous cell carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papillary squamous carcinoma", "shortest_name_length": 28}
{"curie": "UMLS:C1336960", "names": ["VLR GIST", "Very Low Risk Gastrointestinal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Very Low Risk Gastrointestinal Stromal Tumor", "shortest_name_length": 8}
{"curie": "MONDO:0001250", "names": ["keratomalacia", "Keratomalacia", "Keratomalacia NOS", "Keratomalacia, NOS", "Keratomalacia (disorder)", "keratomalacia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratomalacia", "shortest_name_length": 13}
{"curie": "MONDO:0013672", "names": ["CHROMOSOME 15q25 DELETION SYNDROME", "chromosome 15q25 deletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 15q25 deletion syndrome", "shortest_name_length": 34}
{"curie": "UMLS:C4331453", "names": ["Unknown Primary Tumor (Except for EBV-Related and HPV-Related Tumors) and Metastatic Cervical Adenopathy by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unknown Primary Tumor (Except for EBV-Related and HPV-Related Tumors) and Metastatic Cervical Adenopathy by AJCC v8 Stage", "shortest_name_length": 121}
{"curie": "MONDO:0009185", "names": ["KTZS", "Kohlschutter syndrome", "KOHLSCHUTTER SYNDROME", "Kohlschutter's syndrome", "epilepsy and Yellow teeth", "EPILEPSY AND YELLOW TEETH", "epilepsy and yellow teeth", "Epilepsy and yellow teeth", "Kohlschutter-Tonz syndrome", "KOHLSCHUTTER-TONZ SYNDROME", "Kohlschutter Tonz syndrome", "Kohlschutter-Tonz Syndrome", "Kohlschütter-Tönz syndrome", "KOHLSCHUTTER-Tonz syndrome", "Amelocerebrohypohidrotic syndrome", "amelocerebrohypohidrotic syndrome", "Kohlschutter's syndrome (disorder)", "Kohlschutter's syndrome (diagnosis)", "epilepsy dementia amelogenesis imperfecta", "Epilepsy dementia amelogenesis imperfecta", "Epilepsy, dementia and amelogenesis imperfecta", "Epilepsy, Dementia, And Amelogenesis Imperfecta", "EPILEPSY, DEMENTIA, AND AMELOGENESIS IMPERFECTA", "Epilepsy, mental deterioration and yellow teeth", "epilepsy, dementia, and amelogenesis imperfecta", "Epilepsy-dementia-amelogenesis imperfecta syndrome", "epilepsy-dementia-amelogenesis imperfecta syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amelocerebrohypohidrotic syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C5420040", "names": ["Sinonasal Respiratory Epithelial Adenomatoid Hamartoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Respiratory Epithelial Adenomatoid Hamartoma", "shortest_name_length": 54}
{"curie": "MONDO:0044748", "names": ["Anaplasmoses", "anaplasmosis in cattle"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anaplasmosis in cattle", "shortest_name_length": 12}
{"curie": "MONDO:0015691", "names": ["HES", "eosinophilia", "EOSINOPHILIA", "Eosinophilia", "EOSINOPHILIAS", "eosinophilias", "Eosinophilia, NOS", "Hypereosinophilia", "Hypereosinophilias", "high eosinophil count", "eosinophils increased", "increased eosinophils", "Increased eosinophils", "EOSINOPHILS INCREASED", "eosinophilia (diagnosis)", "hypereosinophilic disease", "Eosinophilia, unspecified", "Eosinophilic leukocytosis", "eosinophilic leukocytosis", "Hypereosinophilic syndrome", "Hypereosinophilic Syndrome", "hypereosinophilic disorder", "hypereosinophilic syndrome", "HYPEREOSINOPHILIC SYNDROME", "Syndrome, Hypereosinophilic", "Hyper Eosinophilic Syndrome", "High blood eosinophil count", "Hypereosinophilic Syndromes", "Syndromes, Hypereosinophilic", "Hypereosinophilic syndrome [HES]", "HES - hypereosinophilic syndrome", "eosinophilic leukocytosis (diagnosis)", "Hypereosinophilic syndrome (disorder)", "Disorder characterized by eosinophilia", "Disorder characterised by eosinophilia", "hypereosinophilic syndrome (diagnosis)", "Hypereosinophilic syndrome [HES], unspecified", "Disorder characterized by eosinophilia (disorder)", "Hypereosinophilic syndrome (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypereosinophilic syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C0854431", "names": ["Injection site blister", "Injection site blisters", "Injection site vesicles", "Blister at injection site", "Vesicles at injection site", "Injection site blister (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Blister at injection site", "shortest_name_length": 22}
{"curie": "UMLS:C0562057", "names": ["burn throat", "throat burn", "throat; burn", "burn; throat", "burns throat", "burned throat", "throat burning", "burning throat", "Burn of throat", "burning in throat", "Burning in throat", "Burn of throat (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Burn of throat", "shortest_name_length": 11}
{"curie": "MONDO:0035433", "names": ["LGMD1I", "LGMD type D4", "calpain-3-related LGMD D4", "limb-girdle muscular dystrophy type D4", "calpain-3-related limb-girdle muscular dystrophy D4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "calpain-3-related limb-girdle muscular dystrophy D4", "shortest_name_length": 6}
{"curie": "MONDO:0012495", "names": ["SEMDG", "NANS DEFICIENCY", "Nans deficiency", "SEMD Genevieve type", "SEMD, Geneviève type", "SEMD, Genevieve type", "SEMD, GENEVIEVE TYPE", "SEMD, Genevieve Type", "Spondyloepimetaphyseal dysplasia Geneviève type", "spondyloepimetaphyseal dysplasia Genevieve type", "Spondyloepimetaphyseal dysplasia Genevieve type", "SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE", "Spondyloepimetaphyseal dysplasia, Genevieve type", "spondyloepimetaphyseal dysplasia, Genevieve type", "spondyloepimetaphyseal dysplasia, Genevieve-type", "Spondyloepimetaphyseal dysplasia, Geneviève type", "spondyloepimetaphyseal dysplasia, Geneviève type", "spondyloepimetaphyseal dysplasia, Camera-Genevieve type", "SEMDG - spondyloepimetaphyseal dysplasia Genevieve type", "Spondyloepimetaphyseal dysplasia Genevieve type (disorder)", "spondyloepimetaphyseal dysplasia, Genevieve type (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepimetaphyseal dysplasia, Genevieve type", "shortest_name_length": 5}
{"curie": "UMLS:C4528591", "names": ["Stage IIIC Breast Cancer", "Prognostic Stage IIIC Breast Cancer AJCC v8", "Prognostic Stage IIIC Breast Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prognostic Stage IIIC Breast Cancer AJCC v8", "shortest_name_length": 24}
{"curie": "UMLS:C5670542", "names": ["Posterior Fossa Ependymoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Posterior Fossa Ependymoma", "shortest_name_length": 26}
{"curie": "MONDO:0003352", "names": ["Colon Sarcoma", "colon sarcoma", "colonic sarcoma", "Colonic sarcoma", "Colonic Sarcoma", "Sarcoma of Colon", "sarcoma of colon", "Sarcoma of the Colon", "sarcoma of the colon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colon sarcoma", "shortest_name_length": 13}
{"curie": "DOID:0060314", "names": ["PGL", "persistent generalized lymphadenopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "persistent generalized lymphadenopathy", "shortest_name_length": 3}
{"curie": "MONDO:0030455", "names": ["DYT31", "dystonia 31", "DYSTONIA 31", "ZECH-BOESCH SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dystonia 31", "shortest_name_length": 5}
{"curie": "UMLS:C0751448", "names": ["Familial Polyneuropathy", "familial polyneuropathy", "Inherited Polyneuropathy", "Polyneuropathy, Familial", "inherited polyneuropathy", "Polyneuropathy, Inherited", "Familial Polyneuropathies", "Inherited Polyneuropathies", "Polyneuropathies, Familial", "polyneuropathy; hereditary", "hereditary; polyneuropathy", "Polyneuropathies, Inherited"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Polyneuropathy, Familial", "shortest_name_length": 23}
{"curie": "MONDO:0018879", "names": ["LPP", "Kossard disease", "lichen follicularis", "Lichen planopilaris", "Lichen follicularis", "lichen planopilaris", "Lichen plano-pilaris", "Graham-Little syndrome", "follicular lichen planus", "Follicular lichen planus", "planus; lichen, follicular", "lichen planus follicularis", "Lichen planus follicularis", "lichen; planus, follicular", "Lichen planopilaris (disorder)", "Lassueur-Graham-Little syndrome", "Piccardi-Lasseur-Little syndrome", "Follicular lichen planus tumidus", "lichen planopilaris classic type", "Lichen planus follicularis tumidus", "Lichen planus tumidus follicularis", "frontal fibrosing alopecia (subtype)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lichen planopilaris", "shortest_name_length": 3}
{"curie": "MONDO:0010928", "names": ["dwarfism familial with muscle spasms", "DWARFISM, FAMILIAL, WITH MUSCLE SPASMS", "Dwarfism, Familial, With Muscle Spasms", "dwarfism, familial, with muscle spasms", "familial dwarfism and painful muscle spasms"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dwarfism, familial, with muscle spasms", "shortest_name_length": 36}
{"curie": "MONDO:0013807", "names": ["CSNB1E", "Csnb, complete, autosomal recessive", "CSNB, COMPLETE, AUTOSOMAL RECESSIVE", "congenital stationary night blindness 1E", "GPR179 congenital stationary night blindness", "congenital stationary night blindness type 1E", "congenital stationary night blindness - type 1e", "night blindness, congenital stationary, type 1E", "NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1E", "congenital stationary night blindness - type 1e (diagnosis)", "congenital stationary night blindness 1E autosomal recessive", "congenital stationary night blindness caused by mutation in GPR179", "night blindness, congenital stationary (complete), 1E, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital stationary night blindness 1E", "shortest_name_length": 6}
{"curie": "MONDO:0030855", "names": ["OIEDS2", "OIEDS Syndrome 2", "OIEDS SYNDROME 2", "COMBINED OSTEOGENESIS IMPERFECTA AND EHLERS-DANLOS SYNDROME 2", "combined osteogenesis imperfecta and Ehlers-Danlos syndrome 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined osteogenesis imperfecta and Ehlers-Danlos syndrome 2", "shortest_name_length": 6}
{"curie": "UMLS:C3898888", "names": ["Hepatocellular Carcinoma BCLC Staging", "Hepatocellular Carcinoma by BCLC Stage", "BCLC Staging for Hepatocellular Carcinoma", "Hepatocellular Carcinoma Barcelona Clinic Liver Cancer Staging", "Hepatocellular Carcinoma by Barcelona Clinic Liver Cancer Stage", "Barcelona Clinic Liver Cancer Staging for Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatocellular Carcinoma by BCLC Stage", "shortest_name_length": 37}
{"curie": "MONDO:0044137", "names": ["VITREOUS DISORDER", "Vitreous disorder", "Disorder vitreous", "disorder vitreous", "vitreous disorder", "DISORDER VITREOUS", "vitreous disorders", "Disorder of vitreous", "Vitreus disorder NOS", "vitreous body disease", "Vitreous disorder NOS", "VITREOUS DISORDER NOS", "Vitreous Body Disorder", "Vitreous disorder, NOS", "vitreous body disorder", "disease of vitreous body", "disorder of vitreous body", "Disorder of vitreous body", "Disorders of vitreous body", "Disorder of vitreous cavity", "vitreous disorders (diagnosis)", "Disorder of vitreous body, NOS", "DISORDERS OF THE VITREOUS BODY", "disease (or disorder); , vitreous", "vitreous body disease or disorder", "Disorder of vitreous body (disorder)", "disease or disorder of vitreous body", "Unspecified disorder of vitreous body", "Disorder of vitreous body, unspecified", "Disorder of vitreous cavity (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitreous body disorder", "shortest_name_length": 17}
{"curie": "MONDO:0015635", "names": ["comedo nevus of the palm", "Comedo nevus of the palm", "Porokeratotic eccrine nevus", "Linear eccrine nevi with comedones", "linear eccrine Nevus with comedones", "Linear eccrine naevi with comedones", "Linear Eccrine Nevus with Comedones", "Porokeratotic eccrine duct and hair follicle nevus", "porokeratotic eccrine ostial and dermal duct nevus", "Porokeratotic Eccrine Ostial and Dermal Duct Nevus", "Porokeratotic eccrine duct and hair follicle Nevus", "Porokeratotic eccrine ostial and dermal duct nevus", "Porokeratotic Eccrine Duct and Hair Follicle Nevus", "Porokeratotic eccrine duct and hair follicle naevus", "Porokeratotic eccrine ostial and dermal duct naevus", "Porokeratotic eccrine ostial and dermal duct nevus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "porokeratotic eccrine ostial and dermal duct nevus", "shortest_name_length": 24}
{"curie": "MONDO:0006056", "names": ["SCC of breast", "scc of breast", "SCC of Breast", "SCC of the Breast", "scc of the breast", "squamous breast carcinoma", "Squamous Breast Carcinoma", "Squamous Carcinoma of Breast", "squamous carcinoma of breast", "Squamous cell breast carcinoma", "Squamous Cell Breast Carcinoma", "squamous cell breast carcinoma", "Breast Squamous Cell Carcinoma", "breast squamous cell carcinoma", "squamous carcinoma of the breast", "Squamous Carcinoma of the Breast", "squamous cell carcinoma of breast", "Squamous Cell Carcinoma of Breast", "metaplastic squamous cell carcinoma", "squamous cell carcinoma of the breast", "Squamous Cell Carcinoma of the Breast", "Primary Squamous Cell Breast Carcinoma", "primary squamous cell breast carcinoma", "breast primary squamous cell carcinoma", "Primary Squamous Cell Carcinoma of Breast", "primary squamous cell carcinoma of breast", "primary squamous cell carcinoma of the breast", "Primary Squamous Cell Carcinoma of the Breast", "squamous cell carcinoma of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "squamous cell breast carcinoma", "shortest_name_length": 13}
{"curie": "UMLS:C0003944", "names": ["personality", "As If Personality", "Personality, As If", "'as if' personality"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "As If Personality", "shortest_name_length": 11}
{"curie": "MONDO:0001301", "names": ["Merycism", "Rumination", "rumination", "Ruminations", "rumination syndrome", "Rumination Syndrome", "Rumination disorder", "rumination disorder", "Rumination Disorder", "rumination; disorder", "Rumination Disorders", "Rumination Syndromes", "disorder; rumination", "psychogenic rumination", "Rumination psychogenic", "Psychogenic rumination", "Rumination disorder, NOS", "Rumination disorder (disorder)", "rumination disorder (diagnosis)", "Psychogenic rumination (disorder)", "psychogenic rumination (diagnosis)", "Childhood Eating and Feeding Disorders", "Feeding and Eating Disorders of Childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rumination disorder", "shortest_name_length": 8}
{"curie": "UMLS:C0854788", "names": ["recurrent small bowel cancer", "small bowel cancer, recurrent", "Relapsed Small Bowel Carcinoma", "Relapsed Small Intestine Cancer", "Recurrent Small Bowel Carcinoma", "recurrent small intestine cancer", "Relapsed Carcinoma of Small Bowel", "small intestine cancer, recurrent", "Recurrent Small Intestinal Cancer", "Relapsed Small Intestine Carcinoma", "Relapsed Cancer of Small Intestine", "Recurrent Carcinoma of Small Bowel", "Recurrent Cancer of Small Intestine", "Small intestine carcinoma recurrent", "Recurrent Small Intestine Carcinoma", "Recurrent Small Intestinal Carcinoma", "Small Intestine Carcinoma, Recurrent", "Relapsed Carcinoma of the Small Bowel", "Relapsed Carcinoma of Small Intestine", "Relapsed Cancer of the Small Intestine", "Recurrent Carcinoma of Small Intestine", "Recurrent Carcinoma of the Small Bowel", "Recurrent Cancer of the Small Intestine", "Relapsed Carcinoma of the Small Intestine", "Recurrent Carcinoma of the Small Intestine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small intestine carcinoma recurrent", "shortest_name_length": 28}
{"curie": "UMLS:C3544188", "names": ["Exposure via ingestion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Exposure via ingestion", "shortest_name_length": 22}
{"curie": "MONDO:0005411", "names": ["gallbladder Ca", "gallbladder ca", "Gallbladder Ca", "cancer gallbladder", "gallbladder cancer", "Gallbladder Cancer", "GALLBLADDER CANCER", "Gallbladder cancer", "Gallbladder Cancers", "Cancer, Gallbladder", "gall bladder cancer", "Gall Bladder Cancer", "Gallbladder--Cancer", "gallbladder cancers", "Cancers, Gallbladder", "Cancer, Gall Bladder", "Gall Bladder Cancers", "Bladder Cancer, Gall", "gallbladder neoplasm", "of gallbladder cancer", "Cancers, Gall Bladder", "Cancer of Gallbladder", "cancer of gallbladder", "Bladder Cancers, Gall", "cancer of gall bladder", "Gallbladder cancer NOS", "tumor of the gallbladder", "Cancer of the Gallbladder", "cancer of the gallbladder", "Malignant Gallbladder Tumor", "malignant gallbladder tumor", "gallbladder tumor or cancer", "Gallbladder cancer localised", "Gallbladder cancer localized", "localized gallbladder cancer", "gallbladder cancer, localized", "Malignant Gallbladder Neoplasm", "malignant gallbladder neoplasm", "malignant tumor of gallbladder", "Malignant Tumor of Gallbladder", "gallbladder malignant neoplasm", "Malignant tumor of gallbladder", "Gallbladder Malignant Neoplasm", "Gallbladder neoplasms malignant", "Malignant tumour of gallbladder", "malignant tumour of gallbladder", "malignant gall bladder neoplasm", "malignant neoplasm of gallbladder", "Malignant Neoplasm of Gallbladder", "Malignant neoplasm of gallbladder", "Malignant Tumor of the Gallbladder", "malignant neoplasm of gall bladder", "malignant tumor of the gallbladder", "malignant neoplasm of the gallbladder", "Malignant Neoplasm of the Gallbladder", "Localized Malignant Gallbladder Neoplasm", "localized malignant gallbladder neoplasm", "Malignant tumor of gallbladder (disorder)", "Malignant Neoplasm of Gallbladder Localized", "Malignant neoplasm of gallbladder localised", "Malignant neoplasm of gallbladder localized", "malignant neoplasm of gallbladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gallbladder cancer", "shortest_name_length": 14}
{"curie": "UMLS:C0270858", "names": ["migraine abdominal", "Migraine;abdominal", "abdominal migraine", "Abdominal migraine", "Abdominal Migraine", "abdominal migraines", "abdominal; migraine", "Abdominal Migraines", "Migraine, Abdominal", "migraine; abdominal", "Decapitated migraine", "Migraines, Abdominal", "abdominal migraine headache", "syndrome; abdominal migraine", "Abdominal migraine (disorder)", "abdominal migraine headache (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abdominal Migraine", "shortest_name_length": 18}
{"curie": "UMLS:C1955779", "names": ["Chronic Total Coronary Artery Occlusion", "Chronic total occlusion of coronary artery", "chronic total occlusion of coronary artery", "Chronic total occlusion of coronary artery (disorder)", "chronic total occlusion of coronary artery (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic total occlusion of coronary artery", "shortest_name_length": 39}
{"curie": "MONDO:0018115", "names": ["epidermal nevus syndrome", "Epidermal hamartoma syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermal nevus syndrome", "shortest_name_length": 24}
{"curie": "MONDO:0009042", "names": ["CRANIOTELENCEPHALIC DYSPLASIA", "craniotelencephalic dysplasia", "Craniotelencephalic dysplasia", "Craniotelencephalic dysplasia (disorder)", "Complex of anomalies involving the cranium and brain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniotelencephalic dysplasia", "shortest_name_length": 29}
{"curie": "UMLS:C0854962", "names": ["Stage III Vulvar Cancer", "stage III vulvar cancer", "FIGO Stage III Vulva Carcinoma", "Stage III Vulva Cancer AJCC v6", "Vulva Cancer Stage III AJCC v6", "Vulval Cancer Stage III AJCC v6", "Stage III Vulvar Cancer AJCC v6", "FIGO Stage III Vulvar Carcinoma", "FIGO Stage III Carcinoma of Vulva", "AJCC Stage III Vulva Cancer AJCC v6", "FIGO Stage III Carcinoma of the Vulva"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Vulvar Cancer AJCC v6", "shortest_name_length": 23}
{"curie": "UMLS:C0153570", "names": ["Cancer of exocervix", "Malignant Exocervix Tumor", "Malignant Exocervical Tumor", "Malignant Exocervix Neoplasm", "malignant tumor of exocervix", "Malignant Tumor of Exocervix", "Malignant Exocervical Neoplasm", "Malignant neoplasm of exocervix", "Malignant Neoplasm of Exocervix", "malignant neoplasm of exocervix", "Malignant Tumor of the Exocervix", "Malignant Uterine Exocervix Tumor", "Malignant Neoplasm of the Exocervix", "Malignant Tumor of Uterine Exocervix", "Malignant Uterine Exocervix Neoplasm", "Malignant Neoplasm of Uterine Exocervix", "Malignant Tumor of the Uterine Exocervix", "Malignant neoplasm of exocervix (disorder)", "malignant neoplasm of exocervix (diagnosis)", "Malignant Neoplasm of the Uterine Exocervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant neoplasm of exocervix", "shortest_name_length": 19}
{"curie": "MONDO:0012661", "names": ["KAZA3", "kala-AZAR, susceptibility to, 3", "KALA-AZAR, SUSCEPTIBILITY TO, 3", "susceptibility to visceral leishmaniasis, 3", "leishmaniasis, visceral, susceptibility to, 3", "LEISHMANIASIS, VISCERAL, SUSCEPTIBILITY TO, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "susceptibility to visceral leishmaniasis, 3", "shortest_name_length": 5}
{"curie": "MONDO:0014345", "names": ["RP69", "RETINITIS PIGMENTOSA 69", "retinitis pigmentosa 69", "KIZ retinitis pigmentosa", "retinitis pigmentosa type 69", "retinitis pigmentosa caused by mutation in KIZ"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 69", "shortest_name_length": 4}
{"curie": "UMLS:C0334396", "names": ["Carcinoma with apocrine metaplasia", "Adenocarcinoma with apocrine metaplasia", "Adenocarcinoma with Apocrine Metaplasia", "adenocarcinoma with apocrine metaplasia", "adenocarcinoma with apocrine metaplasia (diagnosis)", "Adenocarcinoma with apocrine metaplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma with apocrine metaplasia", "shortest_name_length": 34}
{"curie": "UMLS:C0041899", "names": ["PERSONALITY UNSTABLE", "Personality unstable", "Unstable personality", "Unstable Personality", "instability; personality", "personality; instability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Personality unstable", "shortest_name_length": 20}
{"curie": "MONDO:0021316", "names": ["minor salivary gland cancer", "cancer of minor salivary gland", "Malignant Minor Salivary Gland Tumor", "malignant minor salivary gland tumor", "Malignant Tumor of Minor Salivary Gland", "Malignant tumor of minor salivary gland", "malignant salivary gland neoplasm minor", "Malignant Minor Salivary Gland Neoplasm", "malignant tumor of minor salivary gland", "malignant minor salivary gland neoplasm", "Malignant tumour of minor salivary gland", "Malignant Neoplasm of Minor Salivary Gland", "Malignant neoplasm of minor salivary gland", "malignant neoplasm of minor salivary gland", "malignant tumor of the minor salivary gland", "Malignant Tumor of the Minor Salivary Gland", "malignant neoplasm of the minor salivary gland", "Malignant Neoplasm of the Minor Salivary Gland", "Malignant tumor of minor salivary gland (disorder)", "malignant neoplasm of minor salivary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant tumor of minor salivary gland", "shortest_name_length": 27}
{"curie": "UMLS:C0178546", "names": ["child mental disorder", "child mental disorders", "Childhood Mental Disorder", "childhood disorders mental", "Mental disorder in childhood", "Pediatric Psychiatric Disorder", "childhood psychiatric disorders", "Mental disorder in childhood, NOS", "Mental disorder in childhood (disorder)", "childhood psychiatric disorders (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mental disorder in childhood", "shortest_name_length": 21}
{"curie": "MONDO:0019035", "names": ["PB", "pancreatoblastoma", "Pancreatoblastoma", "[M] Pancreatoblastoma", "Pancreatoblastoma (disorder)", "pancreatoblastoma (diagnosis)", "Pancreatoblastoma (morphologic abnormality)", "pancreatoblastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatoblastoma", "shortest_name_length": 2}
{"curie": "UMLS:C5419534", "names": ["Metastatic Extrahepatic Cholangiocarcinoma", "Metastatic Distal Bile Duct Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Distal Bile Duct Adenocarcinoma", "shortest_name_length": 42}
{"curie": "UMLS:C1336318", "names": ["Stage II Small Cell Lung Cancer", "Stage II Small Cell Lung Carcinoma", "Stage II Small Cell Carcinoma of Lung", "Stage II Small Cell Carcinoma of the Lung", "Stage II Lung Small Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Lung Small Cell Carcinoma AJCC v7", "shortest_name_length": 31}
{"curie": "MONDO:0032696", "names": ["OOMD6", "OOCYTE MATURATION DEFECT 6", "oocyte maturation defect 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oocyte maturation defect 6", "shortest_name_length": 5}
{"curie": "MONDO:0008589", "names": ["tremor of intention, ataxia, and lipofuscinosis", "TREMOR OF INTENTION, ATAXIA, AND LIPOFUSCINOSIS", "Tremor of Intention, Ataxia, and Lipofuscinosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tremor of intention, ataxia, and lipofuscinosis", "shortest_name_length": 47}
{"curie": "UMLS:C0542117", "names": ["Acquired Spider Nevus", "NEVUS SPIDER ACQUIRED", "Nevus spider acquired", "Naevus spider acquired", "Acquired Nevus Araneus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Naevus spider acquired", "shortest_name_length": 21}
{"curie": "UMLS:C0394016", "names": ["Traumatic Coma", "Coma;traumatic", "traumatic coma", "Traumatic coma", "Coma, Traumatic", "Post-Trauma Coma", "Coma, Post Trauma", "Coma, Post-Trauma", "Post-Trauma Comas", "Comas, Post-Trauma", "Post-traumatic coma", "Post-Traumatic Coma", "Coma, Post Traumatic", "Coma, Post-Traumatic", "Post Head Injury Coma", "Post-Head Injury Coma", "Post-Head Injury Comas", "Coma, Post Head Injury", "Coma, Post-Head Injury", "Comas, Post-Head Injury", "Post-traumatic coma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Coma, Post-Head Injury", "shortest_name_length": 14}
{"curie": "MONDO:0003721", "names": ["renal osteosarcoma", "Renal Osteosarcoma", "Kidney Osteosarcoma", "kidney osteosarcoma", "osteosarcoma of kidney", "Osteosarcoma of Kidney", "renal Osteogenic sarcoma", "renal osteogenic sarcoma", "Renal Osteogenic Sarcoma", "kidney osteogenic sarcoma", "Kidney Osteogenic Sarcoma", "Osteosarcoma of the Kidney", "osteosarcoma of the kidney", "osteogenic sarcoma of kidney", "Osteogenic Sarcoma of Kidney", "kidney osteosarcoma (disease)", "Renal Extraskeletal Osteosarcoma", "Osteogenic Sarcoma of the Kidney", "osteogenic sarcoma of the kidney", "renal extraskeletal osteosarcoma", "kidney extraskeletal osteosarcoma", "Kidney Extraskeletal Osteosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kidney osteogenic sarcoma", "shortest_name_length": 18}
{"curie": "MONDO:0009407", "names": ["hypertrophic neuropathy and cataract", "HYPERTROPHIC NEUROPATHY AND CATARACT", "Hypertrophic Neuropathy And Cataract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophic neuropathy and cataract", "shortest_name_length": 36}
{"curie": "MONDO:0012280", "names": ["GOSHS", "Goldberg-Shprintzen syndrome", "GOLDBERG-SHPRINTZEN SYNDROME", "Megacolon microcephaly syndrome", "megacolon-microcephaly syndrome", "Megacolon-microcephaly syndrome", "Goldberg Shprintzen megacolon syndrome", "GOLDBERG-SHPRINTZEN MEGACOLON SYNDROME", "Goldberg-Shprintzen megacolon syndrome", "Goldberg Shprintzen megacolon syndrome (disorder)", "Goldberg Shprintzen megacolon syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Goldberg-Shprintzen megacolon syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C1336423", "names": ["Stage IV Liver Cancer", "Stage IV Liver Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Liver Cancer", "shortest_name_length": 21}
{"curie": "MONDO:0100485", "names": ["KCNH1 related disorder", "KCNH1 associated disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "KCNH1 associated disorder", "shortest_name_length": 22}
{"curie": "MONDO:0004898", "names": ["Total circumpapillary dystrophy of choroid", "total circumpapillary dystrophy of choroid", "circumpapillary dystrophy of choroid, total", "Circumpapillary dystrophy of choroid, total", "total circumpapillary hereditary choroidal dystrophy", "Total circumpapillary dystrophy of choroid (disorder)", "total circumpapillary hereditary choroidal dystrophy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "total circumpapillary dystrophy of choroid", "shortest_name_length": 42}
{"curie": "MONDO:0016164", "names": ["herpetiform pemphigus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "herpetiform pemphigus", "shortest_name_length": 21}
{"curie": "UMLS:C0853895", "names": ["disorder; mental, due to general medical condition", "Mental Disorders due to General Medical Conditions", "mental; disorder, due to general medical condition", "Mental disorder due to a general medical condition", "Mental Disorder Due to a General Medical Condition", "Mental disorder NOS due to a general medical condition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mental disorder due to a general medical condition", "shortest_name_length": 50}
{"curie": "MONDO:0016287", "names": ["cervical adenoid basal carcinoma", "adenoid basal carcinoma of the cervix uteri", "uterine cervix skin adenoid basal cell carcinoma", "skin adenoid basal cell carcinoma of uterine cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenoid basal carcinoma of the cervix uteri", "shortest_name_length": 32}
{"curie": "UMLS:C0276108", "names": ["Psittacosis", "Chlamydiosis", "chlamydiosis", "Chlamydiosis NOS", "Chlamydia psittaci", "psittaci; Chlamydia", "Chlamydia; psittaci", "Chlamydia psittaci infection", "chlamydia infection psittaci", "Chlamydia psittaci infections", "infection; Chlamydia psittaci", "CHLAMYDIA PSITACCI INFECTIONS", "Chlamydophila psittaci Infection", "Chlamydia psitacci infection, NOS", "Chlamydia; infection, Chlamydia psittaci"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chlamydia psittaci infection", "shortest_name_length": 11}
{"curie": "UMLS:C4684879", "names": ["Metastatic Bile Duct Cancer", "Metastatic Bile Duct Carcinoma", "Metastatic Biliary Tract Cancer", "Metastatic Biliary Tract Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Bile Duct Carcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0002116", "names": ["exocrine pancreas cancer", "pancreatic exocrine tumor", "exocrine pancreatic cancer", "tumor of exocrine pancreas", "Pancreatic exocrine cancer", "pancreatic exocrine cancer", "cancer of exocrine pancreas", "malignant exocrine pancreas tumor", "Malignant Exocrine Pancreas Tumor", "Malignant tumor of exocrine pancreas", "Malignant Tumor of Exocrine Pancreas", "malignant exocrine pancreas neoplasm", "Malignant Exocrine Pancreas Neoplasm", "malignant tumor of exocrine pancreas", "Malignant tumour of exocrine pancreas", "malignant tumour of exocrine pancreas", "pancreatic neoplasm malignant exocrine", "malignant neoplasm of exocrine pancreas", "Malignant Neoplasm of Exocrine Pancreas", "Malignant Tumor of the Exocrine Pancreas", "malignant tumor of the exocrine pancreas", "Malignant Neoplasm of the Exocrine Pancreas", "malignant neoplasm of the Exocrine pancreas", "malignant neoplasm of the exocrine pancreas", "Malignant tumor of exocrine pancreas (disorder)", "malignant neoplasm of exocrine pancreas (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant exocrine pancreas neoplasm", "shortest_name_length": 24}
{"curie": "UMLS:C4287976", "names": ["Warthin-Like Variant Thyroid Gland Papillary Carcinoma", "Warthin Tumor-Like Variant Thyroid Gland Papillary Cancer", "Warthin Tumor-Like Variant Thyroid Gland Papillary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Warthin-Like Variant Thyroid Gland Papillary Carcinoma", "shortest_name_length": 54}
{"curie": "MONDO:0024485", "names": ["papillary urothelial hyperplasia", "Papillary Urothelial Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papillary urothelial hyperplasia", "shortest_name_length": 32}
{"curie": "MONDO:0009485", "names": ["kos", "KOS", "BPIDS", "KAUFMAN OCULOCEREBROFACIAL SYNDROME", "Kaufman oculocerebrofacial syndrome", "Oculocerebrofacial syndrome Kaufman type", "oculocerebrofacial syndrome, Kaufman type", "Oculocerebrofacial syndrome, Kaufman type", "oculocerebrofacial syndrome, Kaufman-type", "Oculocerebrofacial syndrome Kaufman type (disorder)", "oculocerebrofacial syndrome, Kaufman-type (diagnosis)", "blepharophimosis-ptosis-intellectual disability syndrome", "BLEPHAROPHIMOSIS-PTOSIS-INTELLECTUAL DISABILITY SYNDROME", "blepharophimosis ptosis intellectual disability syndrome", "severe mental retardation, microcephaly, long narrow face, ocular anomalies, and long thin hands and feet", "severe intellectual disability, microcephaly, long narrow face, ocular anomalies, and long thin hands and feet"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculocerebrofacial syndrome, Kaufman type", "shortest_name_length": 3}
{"curie": "MONDO:0002226", "names": ["tuberculous oophoritis", "Tuberculous oophoritis", "Tuberculous oophoritis (disorder)", "tuberculous oophoritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tuberculous oophoritis", "shortest_name_length": 22}
{"curie": "MONDO:0018492", "names": ["hereditary clear cell renal carcinoma", "Hereditary Clear Cell Renal Cell Cancer", "Hereditary clear cell renal cell cancer", "Hereditary Clear Cell Renal Cell Carcinoma", "hereditary clear cell renal cell carcinoma", "Hereditary clear cell renal cell carcinoma", "hereditary conventional renal cell carcinoma", "renal malignant carcinoma clear cell hereditary", "Hereditary clear cell renal cell adenocarcinoma", "hereditary clear cell renal cell adenocarcinoma", "Hereditary clear cell renal cell carcinoma (disorder)", "Hereditary clear cell renal cell carcinoma (diagnosis)", "hereditary conventional (clear cell) renal cell carcinoma", "Hereditary Conventional (Clear Cell) Renal Cell Carcinoma", "Von Hippel Lindau-Deficient Clear Cell Renal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary clear cell renal cell carcinoma", "shortest_name_length": 37}
{"curie": "UMLS:C0854507", "names": ["Enterovirus Gastroenteritis", "Gastroenteritis enteroviral", "Enterovirus gastroenteritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastroenteritis enteroviral", "shortest_name_length": 27}
{"curie": "MONDO:0018298", "names": ["mona spectrum", "multicentric osteolysis-nodulosis-arthropathy spectrum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multicentric osteolysis-nodulosis-arthropathy spectrum", "shortest_name_length": 13}
{"curie": "UMLS:C5238409", "names": ["Advanced Malignant Female Reproductive System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Malignant Female Reproductive System Neoplasm", "shortest_name_length": 54}
{"curie": "UMLS:C0677691", "names": ["Stage II Aggressive Non-Hodgkin Lymphoma", "stage II contiguous adult aggressive non-Hodgkin lymphoma", "Stage II Contiguous Adult Aggressive Non-Hodgkin Lymphoma", "aggressive, contiguous stage II adult non-Hodgkin lymphoma", "stage II aggressive adult contiguous non-Hodgkin's lymphoma", "Aggressive Contiguous Stage II Adult Non-Hodgkin's Lymphoma", "Stage II Aggressive Adult Contiguous Non-Hodgkin's Lymphoma", "Stage II Contiguous Adult Aggressive Non-Hodgkin's Lymphoma", "Aggressive Contiguous Adult Non-Hodgkin's Lymphoma Stage II", "Adult Aggressive Contiguous Non-Hodgkin's Lymphoma Stage II", "adult aggressive contiguous non-Hodgkin's lymphoma stage II", "stage II contiguous adult aggressive non-Hodgkin's lymphoma", "adult aggressive contiguous stage II non-Hodgkin's lymphoma", "aggressive contiguous adult non-Hodgkin's lymphoma stage II", "aggressive contiguous stage II adult non-Hodgkin's lymphoma", "Adult Aggressive Contiguous Stage II Non-Hodgkin's Lymphoma", "Ann Arbor Stage II Contiguous Adult Aggressive Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage II Contiguous Adult Aggressive Non-Hodgkin Lymphoma", "shortest_name_length": 40}
{"curie": "MONDO:0019800", "names": ["chronic hepatic porphyria", "chronic acute hepatic porphyria", "acute hepatic porphyria, chronic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic hepatic porphyria", "shortest_name_length": 25}
{"curie": "MONDO:0010327", "names": ["CAMR", "MRXS10", "2M3HBA", "HSD10MD", "HSD10 disease", "MHBD deficiency", "MHBD DEFICIENCY", "HSD10 deficiency", "3H2MBD deficiency", "HSD17B10 Deficiency", "HSD17B10 DEFICIENCY", "HSD17B10 deficiency", "HSD10 MITOCHONDRIAL DISEASE", "HSD10 mitochondrial disease", "HSD10 disease, atypical type", "HSD10 deficiency, atypical type", "2-Methyl-3-Hydroxybutyric Aciduria", "2-methyl-3-hydroxybutyric aciduria", "2-Methyl-3-hydroxybutyric aciduria", "mental retardation, X-linked syndromic 10", "MENTAL RETARDATION, X-LINKED, SYNDROMIC 10", "Mental Retardation, X-Linked, Syndromic 10", "mental retardation, X-linked, syndromic 10", "Hydroxyacyl-CoA Dehydrogenase II Deficiency", "hydroxyacyl-CoA dehydrogenase II deficiency", "3-hydroxyacyl-CoA dehydrogenase 2 deficiency", "2-methyl-3-hydroxybutyric aciduria (disorder)", "3-HYDROXYACYL-CoA DEHYDROGENASE II DEFICIENCY", "3-Hydroxyacyl-CoA Dehydrogenase II Deficiency", "HSD10 mitochondrial disease, X-linked dominant", "mental retardation, X-linked, syndromic type 10", "17-Beta-Hydroxysteroid Dehydrogenase X Deficiency", "17-beta-hydroxysteroid dehydrogenase X deficiency", "17-BETA-HYDROXYSTEROID DEHYDROGENASE X DEFICIENCY", "Hydroxyacyl-CoA Dehydrogenase, Type 2, Deficiency", "17-beta-hydroxysteroid dehydrogenase 10 deficiency", "syndromic X-linked intellectual disability type 10", "3-Hydroxyacyl-CoA Dehydrogenase, Type 2, Deficiency", "2-Methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency", "2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency", "3-hydroxy-2-methylbutyryl-CoA dehydrogenase deficiency", "17beta-Hydroxysteroid Dehydrogenase Type 10 Deficiency", "2-Methyl-3-Hydroxybutyryl-CoA Dehydrogenase Deficiency", "2-METHYL-3-HYDROXYBUTYRYL-CoA DEHYDROGENASE DEFICIENCY", "3-Hydroxy-2-Methylbutyryl-CoA Dehydrogenase Deficiency", "17 beta-hydroxysteroid dehydrogenase type 10 deficiency", "[OBSOLETE] Hydroxyacyl-CoA Dehydrogenase, Type 2, Deficiency", "MENTAL RETARDATION WITH CHOREOATHETOSIS AND ABNORMAL BEHAVIOR", "Chorioathetosis With Mental Retardation And Abnormal Behavior", "CHOREOATHETOSIS WITH MENTAL RETARDATION AND ABNORMAL BEHAVIOR", "mental retardation with chorioathetosis and abnormal behavior", "chorioathetosis with mental retardation and abnormal behavior", "Mental Retardation With Chorioathetosis And Abnormal Behavior", "2-Methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency (disorder)", "X-linked intellectual disability-choreoathetosis-abnormal behavior syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HSD10 mitochondrial disease", "shortest_name_length": 4}
{"curie": "MONDO:0043523", "names": ["Itai-Itai", "Itai Itai", "itai itai", "itai-itai", "cadmium poison", "Cadmium toxicity", "CADMIUM TOXICITY", "cadmium toxicity", "Cadmium Poisoning", "cadmium poisoning", "Cadmium poisoning", "cadmium Poisonings", "Poisoning, Cadmium", "Cadmium Poisonings", "poisoning, cadmium", "Poisonings, Cadmium", "Poisonings, cadmium", "poisoning by cadmium", "Cadmium poisoning syndrome", "Cadmium poisoning (disorder)", "disease (or disorder); Itai-itai", "poisoning by cadmium (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cadmium poisoning", "shortest_name_length": 9}
{"curie": "UMLS:C1337018", "names": ["Well Differentiated Malignant Hemangiopericytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Well Differentiated Malignant Hemangiopericytoma", "shortest_name_length": 48}
{"curie": "MONDO:0007531", "names": ["electroencephalographic peculiarity: fronto-precentral beta wave groups", "ELECTROENCEPHALOGRAPHIC PECULIARITY: FRONTO-PRECENTRAL BETA WAVE GROUPS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "electroencephalographic peculiarity: fronto-precentral beta wave groups", "shortest_name_length": 71}
{"curie": "MONDO:0035713", "names": ["FOXG1 syndrome due to intragenic alteration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FOXG1 syndrome due to intragenic alteration", "shortest_name_length": 43}
{"curie": "UMLS:C4554065", "names": ["Brain Glioblastoma", "Childhood Brain Glioblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Brain Glioblastoma", "shortest_name_length": 18}
{"curie": "MONDO:0017030", "names": ["ILD in childhood and adulthood", "interstitial lung disease in childhood and adulthood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "interstitial lung disease in childhood and adulthood", "shortest_name_length": 30}
{"curie": "MONDO:0017097", "names": ["FCD type IB", "isolated focal cortical dysplasia type Ib"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated focal cortical dysplasia type Ib", "shortest_name_length": 11}
{"curie": "MONDO:0012373", "names": ["Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features", "ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features", "ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVE FACIAL FEATURES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features", "shortest_name_length": 81}
{"curie": "MONDO:0019637", "names": ["Small kidneys", "hypoplasia renal", "renal hypoplasia", "Renal hypoplasia", "kidney hypoplasia", "Hypoplastic kidney", "KIDNEY, HYPOPLASIA", "hypoplasia; kidney", "kidney; hypoplasia", "hypoplastic kidney", "hypoplastic kidneys", "Hypoplastic kidneys", "Hypoplasia of kidney", "Hypoplasia of kidneys", "Underdeveloped kidneys", "renal hypoplasia (disease)", "renal hypoplasia (diagnosis)", "Renal hypoplasia, unspecified", "Congenital hypoplasia of kidney", "Congenital hypoplasia of kidney (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal hypoplasia", "shortest_name_length": 13}
{"curie": "MONDO:0012351", "names": ["Zd1", "ZD1", "SD1a", "ZYGODACTYLY 1", "zygodactyly 1", "Zygodactyly 1", "Syndactyly type 1a", "zygodactyly type 1", "Zygodactyly type 1", "syndactyly type 1a", "SD1, Weidenreich type", "Zygodactyly, Weidenreich type", "Syndactyly type 1, Weidenreich type", "syndactyly type 1, Weidenreich type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "zygodactyly type 1", "shortest_name_length": 3}
{"curie": "MONDO:0008213", "names": ["Funnel chest", "funnel chest", "FUNNEL CHEST", "Funnel Chest", "funnel breast", "Funnel Chests", "Funnel breast", "Trichterbrust", "Chest, Funnel", "Chests, Funnel", "chested funnel", "Cobbler's chest", "Hollowed breast", "excavatum pectus", "pectus excavatum", "PECTUS EXCAVATUM", "Pectus excavatum", "Pectus Excavatum", "pectus recurvatum", "pectus; excavatum", "excavatum; pectus", "Pectus recurvatum", "Excavatum, Pectus", "Congenital funnel chest", "funnel chest; congenital", "congenital; funnel chest", "pectus excavatum was seen", "pectus excavatum (disease)", "disorders excavatum pectus", "Congenital pectus excavatum", "Pectus excavatum (disorder)", "congenital pectus excavatum", "pectus excavatum (diagnosis)", "pectus excavatum (funnel breast)", "Congenital pectus excavatum (disorder)", "pectus excavatum (funnel breast) (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pectus excavatum", "shortest_name_length": 12}
{"curie": "UMLS:C1709539", "names": ["Pilar-Associated Mesenchyme Tumor", "Pilar-Associated Mesenchyme Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pilar-Associated Mesenchyme Neoplasm", "shortest_name_length": 33}
{"curie": "MONDO:0021054", "names": ["SARCOMA BONE", "Bone sarcoma", "bone sarcoma", "Bone Sarcoma", "BONE SARCOMA", "Sarcoma bone", "Bone sarcomas", "Osseous Sarcoma", "Sarcoma of bone", "sarcoma of bone", "osseous sarcoma", "Sarcoma of Bone", "Skeletal Sarcoma", "Bone sarcoma NOS", "skeletal sarcoma", "Sarcoma of the Bone", "sarcoma of the bone", "Sarcoma of bone (disorder)", "sarcoma of bone (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bone sarcoma", "shortest_name_length": 12}
{"curie": "MONDO:0016982", "names": ["Angiosarcoma", "angiosarcoma", "angiosarcomas", "Angiosarcomas", "hemangiosarcoma", "Hemangiosarcoma", "vascular sarcoma", "Haemangiosarcoma", "Angiosarcoma NOS", "haemangiosarcoma", "Hemangiosarcomas", "hemangiosarcomas", "Hemangiosarcoma NOS", "Haemangiosarcoma NOS", "blood vessel sarcoma", "angiosarcoma (disease)", "Localized Angiosarcoma", "sarcoma of blood vessel", "Angiosarcoma (disorder)", "angiosarcoma (diagnosis)", "Angiosarcoma Nonmetastatic", "Hemangiosarcoma (disorder)", "hemangiosarcoma, malignant", "HEMANGIOSARCOMA, MALIGNANT", "Non-Metastatic Angiosarcoma", "Malignant Angioendothelioma", "malignant angioendothelioma", "Hemangioendothelial sarcoma", "Angiosarcoma non-metastatic", "Haemangioendothelial sarcoma", "Malignant hemangioendothelioma", "Hemangioendothelioma malignant", "Non-Metastatic Hemangiosarcoma", "Malignant Hemangioendothelioma", "malignant hemangioendothelioma", "Malignant haemangioendothelioma", "Haemangioendothelioma malignant", "Hemangioendothelioma, malignant", "Haemangioendothelioma, malignant", "Angiosarcoma (morphologic abnormality)", "Hemangiosarcoma (morphologic abnormality)", "malignant hemangioendothelioma (diagnosis)", "Hemangioendothelioma, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angiosarcoma", "shortest_name_length": 12}
{"curie": "MONDO:0007342", "names": ["CCF", "Talipes", "talipes", "clubfoot", "Clubfeet", "CLUBFOOT", "Clubfoot", "club foot", "Club feet", "Club foot", "CLUB FOOT", "Club Foot", "Pie Torcido", "Equinovarus", "equinovarus", "Pes equinus", "FOOT CLUBBED", "Pie Torcidos", "clubbed foot", "Clubbed Foot", "CLUBBED FOOT", "Clubfoot, NOS", "Talipes varus", "Pes equinovarus", "Clubbing of feet", "Talipes congenital", "clubfoot disorders", "Congenital Clubfeet", "deformity; clubfoot", "Talipes Equinovarus", "congenital clubfoot", "Congenital Clubfoot", "talipes equinovarus", "clubfoot; deformity", "Congenital clubfoot", "Talipes equinovarus", "congenital club foot", "Clubfeet, Congenital", "equinovarus; talipes", "Club foot congenital", "Congenital club feet", "talipes; equinovarus", "Clubfoot, Congenital", "Clubfoot - congenital", "Clubfoot (congenital)", "Equinovarus deformity", "club foot (diagnosis)", "Congenital talipes NOS", "congenital equinovarus", "Congenital equinovarus", "Congenital clubfoot NOS", "feet talipes equinovarus", "Foot, talipes equinovarus", "TEV - Talipes equinovarus", "equinovarus deformity of foot", "Equinovarus deformity of foot", "Congenital talipes equinovarus", "congenital talipes equinovarus", "Congenital Talipes Equinovarus", "Talipes equinovarus (disorder)", "Talipes equinovarus (clubfoot)", "Talipes Equinovarus, Congenital", "Talipes equinovarus, congenital", "CTEV - Congenital talipes equinovarus", "talipes equinovarus (physical finding)", "equinovarus deformity of foot (finding)", "Congenital talipes equinovarus (disorder)", "congenital talipes equinovarus (diagnosis)", "Familial clubfoot due to PITX1 point mutation", "Familial Clubfoot due to PITX1 Point Mutation", "Hereditary clubfoot due to PITX1 point mutation", "Clubfoot, Congenital, with or without Deficiency of Long Bones and/or Mirror-Image Polydactyly", "clubfoot, congenital, with or without deficiency of long bones and/or mirror-IMAGE polydactyly", "CLUBFOOT, CONGENITAL, WITH OR WITHOUT DEFICIENCY OF LONG BONES AND/OR MIRROR-IMAGE POLYDACTYLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "clubfoot", "shortest_name_length": 3}
{"curie": "MONDO:0023579", "names": ["Kuster Majewski Hammerstein syndrome", "Alopecia macular degeneration growth retardation", "alopecia macular degeneration growth retardation", "alopecia, macular degeneration, and growth retardation", "Alopecia, macular degeneration, and growth retardation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kuster Majewski Hammerstein syndrome", "shortest_name_length": 36}
{"curie": "MONDO:0009342", "names": ["Santos Mateus Leal syndrome", "Santos-Mateus-Leal syndrome", "Hirschsprung disease, deafness and polydactyly", "Hirschsprung disease-deafness-polydactyly syndrome", "Hirschsprung disease-hearing loss-polydactyly syndrome", "Hirschsprung disease with deafness and polydactyly syndrome", "Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness", "Hirschsprung disease with polydactyly, renal agenesis, and deafness", "HIRSCHSPRUNG DISEASE WITH POLYDACTYLY, RENAL AGENESIS, AND DEAFNESS", "Hirschsprung disease with deafness and polydactyly syndrome (disorder)", "Hirschsprung disease associated with polydactyly, unilateral renal agenesis, hypertelorism, and congenital deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hirschsprung disease-hearing loss-polydactyly syndrome", "shortest_name_length": 27}
{"curie": "UMLS:C0853198", "names": ["Gastroenteritis yersinia", "Yersinia gastroenteritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastroenteritis yersinia", "shortest_name_length": 24}
{"curie": "UMLS:C4528634", "names": ["Stage II Acral Lentiginous Melanoma", "Stage II Acral Melanoma AJCC v6 and v7", "Stage II Acral Lentiginous Melanoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Acral Lentiginous Melanoma AJCC v6 and v7", "shortest_name_length": 35}
{"curie": "MONDO:0009800", "names": ["tibia vara, adolescent", "TIBIA VARA, ADOLESCENT", "BLOUNT DISEASE, ADOLESCENT", "Blount disease, adolescent", "OSTEOCHONDROSIS DEFORMANS TIBIAE, ADOLESCENT", "Osteochondrosis deformans tibiae, adolescent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Blount disease, adolescent", "shortest_name_length": 22}
{"curie": "UMLS:C0277556", "names": ["relapse", "Relapse", "DISEASE RELAPSE", "RELAPSED DISEASE", "Relapsed Disease", "disease recurrent", "Recurrent Disease", "Diseases--Relapse", "Recurrent disease", "RECURRENT DISEASE", "recurrent disease", "Disease in relapse", "Recurrent disease, NOS", "Relapse, Site Not Specified", "Recurrent disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent disease", "shortest_name_length": 7}
{"curie": "MONDO:0010257", "names": ["PCSX", "HPCX1", "prostate cancer, hereditary, X-linked 1", "PROSTATE CANCER, HEREDITARY, X-LINKED 1", "PROSTATE CANCER SUSCEPTIBILITY, X-LINKED", "prostate cancer susceptibility, X-linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate cancer, hereditary, X-linked 1", "shortest_name_length": 4}
{"curie": "UMLS:C2062473", "names": ["acute bacterial pyelonephritis", "Acute bacterial pyelonephritis", "Acute pyelonephritis caused by bacterium", "acute bacterial pyelonephritis (diagnosis)", "Acute pyelonephritis caused by bacterium (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute pyelonephritis caused by bacterium", "shortest_name_length": 30}
{"curie": "MONDO:0016463", "names": ["Agammaglobulinemia", "HYPOGAMMAGLOBULINEMIA", "Hypogammaglobulinemia", "hypogammaglobulinemia", "Hypogammaglobulinemias", "Hypogammaglobulinaemia", "HYPOGAMMAGLOBULINAEMIA", "hypogammaglobulinaemia", "Immunoglobulin deficiency", "Hypogammaglobulinemia NOS", "Hypogammaglobulinaemia NOS", "Hypogammaglobulinemia, NOS", "syndromic agammaglobulinemia", "Reduced immunoglobulin levels", "Decreased immunoglobulin level", "Decreased serum immunoglobulin", "syndromic hypogammaglobulinemia", "Decreased immunoglobulin levels", "Decreased serum immunoglobulins", "Hypogammaglobulinemia (finding)", "Decreased antibody level in blood", "hypogammaglobulinemia (diagnosis)", "Hypogammaglobulinemia, unspecified", "Hypogammaglobulinaemia, unspecified", "Decreased circulating antibody level", "syndrome associated with agammaglobulinemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic agammaglobulinemia", "shortest_name_length": 18}
{"curie": "MONDO:0054843", "names": ["CILD38", "primary ciliary dyskinesia 38", "ciliary dyskinesia, PRIMARY, 38", "ciliary dyskinesia, primary, 38", "CILIARY DYSKINESIA, PRIMARY, 38", "primary ciliary dyskinesia 38 with or without situs inversus", "ciliary dyskinesia, Primary, 38, with or without situs inversus", "CILIARY DYSKINESIA, PRIMARY, 38, WITH OR WITHOUT SITUS INVERSUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ciliary dyskinesia, primary, 38", "shortest_name_length": 6}
{"curie": "MONDO:0001356", "names": ["Chlorosis", "chlorosis", "Chloroses", "Ferropenic", "fe defxy anemia", "iron deficiency", "Chlorotic anemia", "Chlorotic anaemia", "chlorotic; anemia", "Ferropenic anemia", "asiderotic anemia", "hypoferric anemia", "ferropenic anemia", "Asiderotic anemia", "anemia; chlorotic", "sideropenic anemia", "Ferropenic anaemia", "asiderotic; anemia", "anemia; asiderotic", "Sideropenic anemia", "Asiderotic anaemia", "anemia; sideropenic", "sideropenic; anemia", "Sideropenic anaemia", "fe deficiency anemia", "iron-deficiency anemia", "Iron deficiency anemia", "ANEMIA IRON DEFICIENCY", "Iron Deficiency Anemia", "Iron-Deficiency Anemia", "Iron-deficiency anemia", "iron deficiency anemia", "Anemia iron deficiency", "IRON DEFICIENCY ANEMIA", "ANEMIA DEFICIENCY IRON", "Anemia, Iron Deficiency", "ANAEMIA IRON DEFICIENCY", "iron deficiency anaemia", "Anaemia;iron deficiency", "Anaemia iron deficiency", "anemia; iron deficiency", "Iron deficiency anemias", "ANEMIA, IRON DEFICIENCY", "Anemia, Iron-Deficiency", "Iron-Deficiency Anemias", "Iron Deficiency Anemias", "Iron deficiency anaemia", "iron deficiency; anemia", "Iron-deficiency anaemia", "iron; deficiency, anemia", "Anemias, Iron Deficiency", "Anemias, Iron-Deficiency", "deficiency; anemia, iron", "Fe deficiency anemia NOS", "anemia; deficiency, iron", "Iron deficiency anemia NOS", "Iron deficiency anemia, NOS", "Iron deficiency anaemia, NOS", "IDA - Iron deficiency anemia", "IDA - Iron deficiency anaemia", "Iron deficiency anemia syndrome", "Iron deficiency anaemia syndrome", "Iron deficiency anemia (disorder)", "iron deficiency anemia (diagnosis)", "Iron deficiency anemia, unspecified", "Iron deficiency anaemia, unspecified", "Other specified iron deficiency anemias"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "iron deficiency anemia", "shortest_name_length": 9}
{"curie": "UMLS:C4553700", "names": ["Stage IVA Uterine Corpus Cancer AJCC v8", "Stage IVA Uterine (including Endometrial) Cancer", "Stage IVA Uterine Corpus Carcinoma or Carcinosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Uterine Corpus Cancer AJCC v8", "shortest_name_length": 39}
{"curie": "MONDO:0032900", "names": ["NEDHAHM", "neurodevelopmental disorder with hypotonia and autistic features with or without hyperkinetic movements", "NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND AUTISTIC FEATURES WITH OR WITHOUT HYPERKINETIC MOVEMENTS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with hypotonia and autistic features with or without hyperkinetic movements", "shortest_name_length": 7}
{"curie": "MONDO:0000588", "names": ["autoimmune disease of gastrointestinal tract", "autoimmune disorder of gastrointestinal tract", "alimentary part of gastrointestinal system autoimmune disease", "autoimmune disease of alimentary part of gastrointestinal system", "alimentary part of gastrointestinal system hypersensitivity reaction type II disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune disorder of gastrointestinal tract", "shortest_name_length": 44}
{"curie": "MONDO:0000172", "names": ["MDDGB", "muscular dystrophy-dystroglycanopathy type B", "muscular dystrophy-dystroglycanopathy, type B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy-dystroglycanopathy, type B", "shortest_name_length": 5}
{"curie": "UMLS:C0919818", "names": ["Anti-neutrophil cytoplasmic antibody positive vasculitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anti-neutrophil cytoplasmic antibody positive vasculitis", "shortest_name_length": 56}
{"curie": "UMLS:C3899529", "names": ["Closed Globe Injury", "Closed globe injury", "Closed eyeball trauma", "Closed injury of globe", "Closed injury of eyeball", "Closed injury of eyeball (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Closed injury of eyeball", "shortest_name_length": 19}
{"curie": "UMLS:C0268940", "names": ["Spermatic cord bleeding", "Spermatic Cord Hemorrhage", "Spermatic cord hemorrhage", "Spermatic cord haemorrhage", "hemorrhage; spermatic cord", "spermatic cord; hemorrhage", "hemorrhage of spermatic cord", "Hemorrhage of spermatic cord", "Haemorrhage of spermatic cord", "Hemorrhage of spermatic cord (disorder)", "hemorrhage of spermatic cord (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemorrhage of spermatic cord", "shortest_name_length": 23}
{"curie": "UMLS:C1516057", "names": ["Astler-Coller A Colorectal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Astler-Coller A Colorectal Carcinoma", "shortest_name_length": 36}
{"curie": "MONDO:0042491", "names": ["CIN", "cervical sil", "Cervical SIL", "Cervix Uteri SIL", "cervix uteri sil", "uterine cervix sil", "Uterine Cervix SIL", "cervix squamous intraepithelial lesion", "Cervix Squamous Intraepithelial Lesion", "Cervical Squamous Intraepithelial Lesion", "cervical squamous intraepithelial lesion", "squamous intraepithelial lesion of cervix", "Squamous Intraepithelial Lesion of Cervix", "Cervical Squamous Intraepithelial Neoplasia", "cervical squamous intraepithelial neoplasia", "Cervix Uteri Squamous Intraepithelial Lesion", "cervix uteri squamous intraepithelial lesion", "Squamous Intraepithelial Lesion of the Cervix", "squamous intraepithelial lesion of the cervix", "uterine cervix squamous intraepithelial lesion", "Uterine Cervix Squamous Intraepithelial Lesion", "Squamous Intraepithelial Lesions of the Cervix", "squamous intraepithelial lesion of cervix uteri", "Squamous Intraepithelial Lesion of Cervix Uteri", "Squamous Intraepithelial Lesion of Uterine Cervix", "squamous intraepithelial lesion of uterine cervix", "squamous intraepithelial lesion of the cervix uteri", "Squamous Intraepithelial Lesion of the Cervix Uteri", "Squamous Intraepithelial Lesion of the Uterine Cervix", "squamous intraepithelial lesion of the uterine cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical squamous intraepithelial neoplasia", "shortest_name_length": 3}
{"curie": "UMLS:C0855051", "names": ["Localized Extraskeletal Osteosarcoma", "Non-Metastatic Extraosseous Osteosarcoma", "Extraskeletal osteosarcoma non-metastatic", "Extraskeletal Osteosarcoma, Nonmetastatic", "Non-Metastatic Extraskeletal Osteosarcoma", "Non-Metastatic Extraskeletal Osteogenic Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extraskeletal osteosarcoma non-metastatic", "shortest_name_length": 36}
{"curie": "UMLS:C2981392", "names": ["Stage IVB Appendix Cancer", "Stage IVB Appendix Carcinoma", "Stage IVB Appendix Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Appendix Carcinoma AJCC v7", "shortest_name_length": 25}
{"curie": "UMLS:C3273215", "names": ["Invasive Breast Lobular Carcinoma, Alveolar Variant", "Invasive Lobular Breast Carcinoma, Alveolar Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Invasive Breast Lobular Carcinoma, Alveolar Variant", "shortest_name_length": 51}
{"curie": "UMLS:C0850639", "names": ["Premalignant Lesion", "premalignant lesion", "pre malignant lesion", "lesions premalignant", "Lesion;pre malignant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Premalignant Lesion", "shortest_name_length": 19}
{"curie": "UMLS:C4288609", "names": ["Nephrotic Syndrome - Infrequently Relapsing"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - Infrequently Relapsing", "shortest_name_length": 43}
{"curie": "MONDO:0003190", "names": ["Middle Ear Carcinoma", "middle Ear carcinoma", "middle ear carcinoma", "carcinoma of middle Ear", "Carcinoma of Middle Ear", "carcinoma of middle ear", "carcinoma of the middle Ear", "carcinoma of the middle ear", "Carcinoma of the Middle Ear", "carcinoma of middle ear (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "middle ear carcinoma", "shortest_name_length": 20}
{"curie": "MONDO:0015600", "names": ["X-linked intellectual disability Cilliers type", "X-linked intellectual disability, Cilliers type", "X-linked intellectual disability Cilliers type (disorder)", "X-linked intellectual disability Cilliers type (diagnosis)", "X-linked intellectual disability-microcephaly-testicular failure syndrome", "X-linked intellectual disability, microcephaly, testicular failure syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability, Cilliers type", "shortest_name_length": 46}
{"curie": "MONDO:0005985", "names": ["Togaviridae disease", "Togavirus Infection", "Togaviridae Disease", "Togaviridae Diseases", "Disease, Togaviridae", "Togavirus infections", "Togavirus Infections", "Infection, Togavirus", "Infections, Togavirus", "Diseases, Togaviridae", "Togaviridae Infection", "Infection, Togaviridae", "Togaviridae Infections", "Infections, Togaviridae", "Disease due to Togaviridae", "DISEASES DUE TO TOGAVIRIDAE", "Disease caused by Togaviridae", "Togaviridae infectious disease", "Disease due to Togaviridae, NOS", "Togaviridae disease or disorder", "Togaviridae caused disease or disorder", "Disease caused by Togaviridae (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Togaviridae infectious disease", "shortest_name_length": 19}
{"curie": "MONDO:0000672", "names": ["form agnosia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "form agnosia", "shortest_name_length": 12}
{"curie": "UMLS:C5556326", "names": ["Early Primary Cutaneous T-Cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Early Primary Cutaneous T-Cell Non-Hodgkin Lymphoma", "shortest_name_length": 51}
{"curie": "MONDO:0007343", "names": ["DIGC", "Acropachy", "acropachy", "CLUBBING OF DIGITS", "Clubbing of Digits", "clubbing of digits", "Hereditary clubbing", "hereditary clubbing", "Hippocratic fingers", "Hereditary acropachy", "Hereditary Acropachy", "ACROPACHY, HEREDITARY", "acropachy, hereditary", "Acropachy, Hereditary", "Hereditary Acropachies", "Acropachies, Hereditary", "Isolated congenital acropachy", "isolated congenital acropachy", "Hereditary clubbing (disorder)", "isolated congenital nail clubbing", "Isolated congenital nail clubbing", "Isolated congenital digital clubbing", "isolated congenital digital clubbing", "digital clubbing, isolated congenital", "DIGITAL CLUBBING, ISOLATED CONGENITAL", "Digital Clubbing, Isolated Congenital"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated congenital digital clubbing", "shortest_name_length": 4}
{"curie": "MONDO:0008013", "names": ["monosomy 9p", "Monosomy 9p", "deletion 9p", "9p monosomy", "9p deletion", "9p syndrome", "9p- syndrome", "Alfi syndrome", "del(9p) syndrome", "monosomy type 9p", "partial monosomy 9p", "deletion 9p syndrome", "Monosomy 9p Syndrome", "MONOSOMY 9p SYNDROME", "monosomy 9p syndrome", "Deletion 9p Syndrome", "9p deletion syndrome", "chromosome 9p deletion", "Monosomy 9p (disorder)", "chromosome 9p monosomy", "Chromosome 9, monosomy 9p", "9p deletion chromosome syndrome", "chromosome deletion 9p syndrome", "CHROMOSOME 9p DELETION SYNDROME", "chromosome 9p deletion syndrome", "Chromosome 9p Deletion Syndrome", "partial deletion of chromosome 9p", "partial monosomy of chromosome 9p", "partial monosomy of the short arm of chromosome 9", "partial deletion of the short arm of chromosome 9", "partial deletion of the short arm of chromosome type 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 9p deletion syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0012404", "names": ["SLEB8", "systemic lupus erythematosus, susceptibility to, 8", "SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "systemic lupus erythematosus, susceptibility to, 8", "shortest_name_length": 5}
{"curie": "UMLS:C1262200", "names": ["Cerebrovascular infarction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebrovascular infarction", "shortest_name_length": 26}
{"curie": "MONDO:0017438", "names": ["agenesis; leg", "leg; agenesis", "Amelia of the leg", "lower limb; amelia", "amelia; lower limb", "Amelia - lower limb", "Amelia of lower limb", "amelia of lower limb", "agenesis; limb, lower", "limb; agenesis, lower", "amelia of a lower limb", "hindlimb non-syndromic amelia", "Congenital absence of lower limb", "limb; absence, congenital, lower", "absence; limb, congenital, lower", "non-syndromic amelia of hindlimb", "amelia of lower limb (diagnosis)", "Congenital complete absence of lower limb", "Congenital absence of lower limb, complete", "Congenital complete absence of lower limb(s)", "Transverse deficiency lower limb - hip level", "Congenital complete absence of lower limb (disorder)", "Transverse deficiency lower limb - hip level (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amelia of lower limb", "shortest_name_length": 13}
{"curie": "MONDO:0021142", "names": ["acquired rippling muscle disease", "sporadic rippling muscle disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired rippling muscle disease", "shortest_name_length": 32}
{"curie": "UMLS:C1377665", "names": ["Childhood CNS Tumor", "pediatric CNS tumor", "Pediatric CNS Tumor", "childhood CNS tumor", "CNS tumor, pediatric", "CNS tumor, childhood", "Childhood CNS Tumors", "Childhood Tumor of CNS", "Pediatric Tumor of CNS", "Childhood CNS Neoplasm", "Pediatric CNS Neoplasm", "Childhood CNS Neoplasms", "Pediatric Neoplasm of CNS", "Childhood Neoplasm of CNS", "Childhood Tumor of the CNS", "Pediatric Tumor of the CNS", "Childhood Neoplasm of the CNS", "Pediatric Neoplasm of the CNS", "Central Nervous System Neoplasm", "Childhood Central Nervous System Tumor", "Pediatric Central Nervous System Tumor", "central nervous system tumor, childhood", "central nervous system tumor, pediatric", "Childhood Central Nervous System Tumors", "Pediatric Tumor of Central Nervous System", "Pediatric Central Nervous System Neoplasm", "Childhood Central Nervous System Neoplasm", "Childhood Tumor of Central Nervous System", "Childhood Central Nervous System Neoplasms", "Pediatric Neoplasm of Central Nervous System", "Childhood Neoplasm of Central Nervous System", "Childhood Tumor of the Central Nervous System", "Pediatric Tumor of the Central Nervous System", "Pediatric Neoplasm of the Central Nervous System", "Childhood Neoplasm of the Central Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Central Nervous System Neoplasm", "shortest_name_length": 19}
{"curie": "UMLS:C4725025", "names": ["Recurrent Acute Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Acute Leukemia", "shortest_name_length": 24}
{"curie": "MONDO:0012968", "names": ["USH1H", "Usher syndrome type 1H", "Usher syndrome type IH", "Usher Syndrome, Type IH", "USHER syndrome, type IH", "Usher syndrome, type 1H", "USHER SYNDROME, TYPE IH"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Usher syndrome type 1H", "shortest_name_length": 5}
{"curie": "UMLS:C0347002", "names": ["metastasis to penis", "Metastases to penis", "Metastasis to penis", "Metastatic tumor to penis", "Metastatic tumour to penis", "metastasis to penis (diagnosis)", "penile neoplasm malignant secondary", "Secondary malignant neoplasm of penis", "Metastatic malignant neoplasm to penis", "Metastatic malignant neoplasm of penis", "Metastatic Malignant Neoplasm in the Penis", "Secondary malignant neoplasm of penis, NOS", "Metastatic malignant neoplasm to penis, NOS", "Metastatic malignant neoplasm to penis (disorder)", "Secondary malignant neoplasm of penis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to penis", "shortest_name_length": 19}
{"curie": "UMLS:C0010957", "names": ["Damage", "damage", "damages", "Damage, NOS", "Tissue Damage", "TISSUE DAMAGE", "tissue damage", "Tissue damage", "damage tissues", "damages tissue", "Tissue damage, NOS", "Damage (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tissue damage", "shortest_name_length": 6}
{"curie": "MONDO:0020794", "names": ["colorectal medullary carcinoma", "Colorectal Medullary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorectal medullary carcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0100269", "names": ["PEX16 related Zellweger spectrum disorder", "peroxisome biogenesis disorder due to PEX16 defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder due to PEX16 defect", "shortest_name_length": 41}
{"curie": "UMLS:C0271979", "names": ["Thalassemia intermedia", "Thalassemia Intermedia", "thalassemia intermedia", "THALASSEMIA INTERMEDIA", "Thalassemia Intermedias", "thalassaemia intermedia", "Intermedia, Thalassemia", "intermedia; thalassemia", "thalassemia; intermedia", "Thalassaemia intermedia", "Intermedias, Thalassemia", "Thalassemia intermedia, NOS", "Thalassemia intermedia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thalassemia Intermedia", "shortest_name_length": 22}
{"curie": "DOID:0081083", "names": ["AML with inv(3)(q21q26.2) or t(3;3)(q21;q26.2)", "AML with inv(3)(q21q26.2) or t(3;3)(q21;q26.2); RPN1-EVI1", "AML with inv(3)(q21.3q26.2) or t(3;3)(q21.3;q26.2); GATA2, MECOM", "Acute myeloid leukemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2)", "acute myeloid leukemia with inv(3) (q21.3;q26.2) or t(3;3) (q21.3;q26.2)", "Acute Myeloid Leukemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2); RPN1-EVI1", "Acute myeloid leukemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2); RPN1-EVI1", "Acute myeloid leukaemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2); RPN1-EVI1", "Acute myeloid leukemia with inv(3)(q21;q26.2) or t(3;3)(q21;q26.2); RPN1-EVI1", "Acute Myeloid Leukemia with inv(3) (q21.3;q26.2) or t(3;3) (q21.3;q26.2); GATA2, MECOM", "Acute myeloid leukemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2); RPN1-EVI1 (disorder)", "Acute myeloid leukemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2); RPN1-EVI1 (diagnosis)", "Acute myeloid leukemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2); RPN1-EVI1 (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia with inv(3) (q21.3;q26.2) or t(3;3) (q21.3;q26.2)", "shortest_name_length": 46}
{"curie": "NCIT:C9023", "names": ["FNCLCC Histologic Grade", "Sarcoma by FNCLCC Grade", "FNCLCC Tumor Grade in Sarcoma", "FNCLCC Histologic Grading System", "Sarcoma by FNCLCC Histologic Grade", "Tumor Differentiation Score in Sarcoma", "Sarcoma by FNCLCC Tumor Differentiation Score", "Histologic Grade (FNCLCC Grading system) (excludes GISTs)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sarcoma by FNCLCC Grade", "shortest_name_length": 23}
{"curie": "MONDO:0013720", "names": ["C4BD", "C4b deficiency", "C4B deficiency", "C4B DEFICIENCY", "Decreased serum complement C4b", "COMPLEMENT COMPONENT 4B DEFICIENCY", "Complement component 4B deficiency", "complement component 4b deficiency", "complement component 4B deficiency", "C4B classic complement early component deficiency", "Decreased circulating complement C4b concentration", "classic complement early component deficiency caused by mutation in C4B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complement component 4b deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0009982", "names": ["retinitis pigmentosa inversa with deafness", "RETINITIS PIGMENTOSA INVERSA WITH DEAFNESS", "Retinitis Pigmentosa Inversa with Deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa inversa with deafness", "shortest_name_length": 42}
{"curie": "MONDO:0000902", "names": ["ACCPN", "HMSN/ACC", "CHARLEVOIX DISEASE", "Charlevoix disease", "Andermann syndrome", "ANDERMANN SYNDROME", "Corpus callosum agenesis neuronopathy", "corpus callosum agenesis neuronopathy", "agenesis of corpus callosum with neuronopathy", "Agenesis of Corpus Callosum with Neuronopathy", "corpus callosum agenesis-neuronopathy syndrome", "Corpus callosum agenesis-neuronopathy syndrome", "agenesis of corpus callosum with polyneuropathy", "Agenesis of Corpus Callosum with Polyneuropathy", "CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY", "Corpus Callosum, Agenesis of, with Neuronopathy", "Agenesis of corpus callosum with polyneuropathy", "corpus callosum, agenesis of, with neuronopathy", "agenesis of corpus callosum with peripheral neuropathy", "Agenesis of corpus callosum with peripheral neuropathy", "Agenesis of Corpus Callosum with Peripheral Neuropathy", "agenesis of the corpus callosum with peripheral neuropathy", "AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY", "Agenesis of the corpus callosum with peripheral neuropathy", "Agenesis of corpus callosum with peripheral neuropathy (disorder)", "peripheral neuropathy associated with agenesis of the corpus callosum", "hereditary motor and sensory neuropathy with agenesis of the corpus callosum", "Hereditary Motor and Sensory Neuropathy with Agenesis of the Corpus Callosum", "Polyneuropathy, sensorimotor, with or without agenesis of the corpus callosum", "polyneuropathy, sensorimotor, with or without agenesis of the corpus callosum", "POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUS CALLOSUM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "agenesis of the corpus callosum with peripheral neuropathy", "shortest_name_length": 5}
{"curie": "MONDO:0009238", "names": ["Folate transport defect", "Folic Acid Transport Defect", "Folic acid transport defect", "folic acid transport defect", "Hereditary folate malabsorption", "congenital folate malabsorption", "Congenital folate malabsorption", "Congenital Folate Malabsorption", "hereditary folate malabsorption", "Hereditary Folate Malabsorption", "Folate Malabsorption, Hereditary", "FOLATE MALABSORPTION, HEREDITARY", "folate malabsorption, hereditary", "Congenital defect of folate absorption", "Congenital malabsorption of folic acid", "congenital defect of folate absorption", "Congenital defect of folate absorption (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary folate malabsorption", "shortest_name_length": 23}
{"curie": "MONDO:0010453", "names": ["MRX92", "XLID92", "X-linked mental retardation 92", "MENTAL RETARDATION, X-LINKED 92", "Mental Retardation, X-Linked 92", "mental retardation, X-linked 92", "intellectual disability, X-linked 92", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 92", "non-syndromic X-linked intellectual disability 92", "mental retardation, X-linked 92, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 92", "shortest_name_length": 5}
{"curie": "MONDO:0017064", "names": ["thoracolumbosacral spina bifida aperta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thoracolumbosacral spina bifida aperta", "shortest_name_length": 38}
{"curie": "UMLS:C0855108", "names": ["Burkitt's tumor stage III", "Burkitt's tumour stage III", "Stage III Burkitt Lymphoma", "Stage III Burkitt's Lymphoma", "Burkitt's Lymphoma Stage III", "Burkitt's lymphoma stage III", "Ann Arbor Stage III Burkitt Lymphoma", "Burkitt's tumor or lymphoma stage III", "Burkitt's tumour or lymphoma stage III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Burkitt Lymphoma", "shortest_name_length": 25}
{"curie": "MONDO:0007990", "names": ["CCSF", "CSCSC", "baby michelin tire", "Michelin-tyre baby", "Michelin-tire baby", "Kunze-Riehm syndrome", "Kunze Riehm syndrome", "lipomatous hypertrophy", "Michelin tire syndrome", "michelin tire syndrome", "Lipomatous hypertrophy", "michelin tire baby syndrome", "MICHELIN TIRE BABY SYNDROME", "Michelin tire baby syndrome", "Michelin-tire baby (disorder)", "Congenital circumferential skin folds", "circumferential skin creases of limbs", "congenital circumferential skin folds", "circumferential ringed creases of limbs", "circumferential skin creases, Kunze type", "Circumferential skin creases, Kunze type", "skin creases, multiple benign ring-shaped, of limbs", "Skin creases, multiple benign ring-shaped, of limbs", "SKIN CREASES, MULTIPLE BENIGN RING-SHAPED, OF LIMBS", "multiple benign circumferential skin creases on limbs", "Multiple benign circumferential skin creases on limbs"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple benign circumferential skin creases on limbs", "shortest_name_length": 4}
{"curie": "UMLS:C0024304", "names": ["Mixed Lymphoma", "Lymphoma, Mixed", "Mixed Lymphomas", "Mixed Cell Lymphoma", "Mixed-Cell Lymphoma", "Lymphoma, Mixed Cell", "Lymphoma, Mixed-Cell", "Mixed-Cell Lymphomas", "Mixed lymphocytic-histiocytic lymphoma", "Mixed Lymphocytic-Histiocytic Lymphoma", "Lymphocytic-Histiocytic Lymphoma, Mixed", "Mixed Lymphocytic-Histiocytic Lymphomas", "Lymphoma, Mixed Lymphocytic Histiocytic", "Lymphoma, Mixed Lymphocytic-Histiocytic", "Lymphocytic-Histiocytic Lymphomas, Mixed"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoma, Mixed-Cell", "shortest_name_length": 14}
{"curie": "UMLS:C5236094", "names": ["Nasal Cavity Papilloma", "Nasal Cavity Schneiderian Papilloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasal Cavity Papilloma", "shortest_name_length": 22}
{"curie": "MONDO:0012477", "names": ["RP33", "RP 33", "RETINITIS PIGMENTOSA 33", "retinitis pigmentosa 33", "Retinitis Pigmentosa 33", "retinitis pigmentosa type 33", "SNRNP200 retinitis pigmentosa", "RETINITIS PIGMENTOSA 33 (disorder)", "retinitis pigmentosa caused by mutation in SNRNP200"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 33", "shortest_name_length": 4}
{"curie": "UMLS:C1711295", "names": ["Reactive Vascular Proliferation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reactive Vascular Proliferation", "shortest_name_length": 31}
{"curie": "UMLS:C5420400", "names": ["Primordial Odontogenic Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primordial Odontogenic Tumor", "shortest_name_length": 28}
{"curie": "MONDO:0018595", "names": ["single-organ PAN", "single-organ polyarteritis nodosa", "single-organ periarteritis nodosa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "single-organ polyarteritis nodosa", "shortest_name_length": 16}
{"curie": "UMLS:C4551534", "names": ["Cervical Cancer Stage IB", "Stage IB Cervical Cancer", "AJCC Stage IB Cervical Cancer", "FIGO Stage IB Cervix Carcinoma", "Stage IB Cervical Cancer AJCC v6", "FIGO Stage IB Cervical Carcinoma", "Stage IB Cervical Cancer AJCC v7", "FIGO Stage IB Carcinoma of Cervix", "FIGO Stage IB Cervix Uteri Carcinoma", "FIGO Stage IB Carcinoma of the Cervix", "FIGO Stage IB Uterine Cervix Carcinoma", "FIGO Stage IB Carcinoma of Cervix Uteri", "Stage IB Cervical Cancer AJCC v6 and v7", "FIGO Stage IB Carcinoma of Uterine Cervix", "FIGO Stage IB Carcinoma of the Cervix Uteri", "FIGO Stage IB Carcinoma of the Uterine Cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Cervical Cancer AJCC v6 and v7", "shortest_name_length": 24}
{"curie": "MONDO:0008643", "names": ["veins, pattern of, on anterior thorax", "VEINS, PATTERN OF, ON ANTERIOR THORAX"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "veins, pattern of, on anterior thorax", "shortest_name_length": 37}
{"curie": "MONDO:0030009", "names": ["APMR4", "ALOPECIA-MENTAL RETARDATION SYNDROME 4", "alopecia-mental retardation syndrome 4", "ALOPECIA-INTELLECTUAL DISABILITY SYNDROME 4", "alopecia-intellectual disability syndrome 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alopecia-intellectual disability syndrome 4", "shortest_name_length": 5}
{"curie": "MONDO:0006041", "names": ["Lung NET", "lung carcinoid", "carcinoid tumor lung", "carcinoid lung tumor", "lung carcinoid tumor", "Lung Carcinoid Tumor", "Lung carcinoid tumor", "carcinoid lung tumour", "Lung carcinoid tumour", "carcinoid lung tumors", "Carcinoid tumor of lung", "of carcinoid lung tumor", "Carcinoid Tumor of Lung", "carcinoid tumor of lung", "CARCINOID TUMOR OF LUNG", "Carcinoid tumour of lung", "Carcinoid tumor pulmonary", "pulmonary carcinoid tumor", "Pulmonary Carcinoid Tumor", "Pulmonary carcinoid tumor", "Lung Neuroendocrine Tumor", "carcinoid pulmonary tumors", "Carcinoid tumour pulmonary", "carcinoid tumor, pulmonary", "Pulmonary carcinoid tumour", "carcinoid tumor of the lung", "Carcinoid Tumor of the Lung", "lung carcinoid tumor (disease)", "carcinoid tumor (disease) of lung", "Carcinoid tumor of lung (disorder)", "carcinoid tumor of lung (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung carcinoid tumor", "shortest_name_length": 8}
{"curie": "MONDO:0015627", "names": ["multiple epiphyseal dysplasia due to collagen 9 anomaly", "Multiple epiphyseal dysplasia due to collagen 9 anomaly", "Multiple epiphyseal dysplasia due to collagen 9 anomaly (disorder)", "Multiple epiphyseal dysplasia due to collagen 9 anomaly (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple epiphyseal dysplasia due to collagen 9 anomaly", "shortest_name_length": 55}
{"curie": "UMLS:C1334174", "names": ["Infectious Mononucleosis-like PTLD", "Infectious Mononucleosis-Like Post-Transplant Lymphoproliferative Disorder", "infectious mononucleosis-like post-transplant lymphoproliferative disorder", "Infectious mononucleosis-like post-transplant lymphoproliferative disorder", "Infectious mononucleosis-like post-transplant lymphoproliferative disorder (disorder)", "infectious mononucleosis-like post-transplant lymphoproliferative disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infectious mononucleosis-like post-transplant lymphoproliferative disorder", "shortest_name_length": 34}
{"curie": "UMLS:C2981267", "names": ["Stage I Differentiated Thyroid Gland Cancer", "Stage I Differentiated Thyroid Gland Carcinoma", "Stage I Differentiated Thyroid Gland Carcinoma AJCC v7", "Stage I Thyroid Gland Papillary or Follicular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Differentiated Thyroid Gland Carcinoma AJCC v7", "shortest_name_length": 43}
{"curie": "MONDO:0018605", "names": ["disorders of pentose/polyol metabolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorders of pentose/polyol metabolism", "shortest_name_length": 38}
{"curie": "UMLS:C1513034", "names": ["Maturing Ganglioneuroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Maturing Ganglioneuroma", "shortest_name_length": 23}
{"curie": "MONDO:0015903", "names": ["HALP1", "CETP Deficiency", "High blood HDL level", "hyperalphalipoproteinemia", "Hyperalphalipoproteinemia", "Hyperalphalipoproteinaemia", "Hyperalphalipoproteinemia (disorder)", "hyperalphalipoproteinemia (diagnosis)", "Increased HDL cholesterol concentration", "Cholesteryl ester transfer protein deficiency", "Cholesteryl Ester Transfer Protein Deficiency", "Increased circulating high-density lipoprotein levels"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperalphalipoproteinemia", "shortest_name_length": 5}
{"curie": "MONDO:0032870", "names": ["IDDSSBA", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH SHORT STATURE AND BEHAVIORAL ABNORMALITIES", "intellectual developmental disorder with short stature and behavioral abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder with short stature and behavioral abnormalities", "shortest_name_length": 7}
{"curie": "UMLS:C5206456", "names": ["Stage IVB Cervical Cancer FIGO 2018", "Stage IVB Cervical Carcinoma FIGO 2018"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Cervical Cancer FIGO 2018", "shortest_name_length": 35}
{"curie": "OMIM:616903", "names": ["THPM2", "NUDT15 deficiency", "NUDT15 DEFICIENCY", "Thiopurine poor metaboliser 2", "Thiopurine poor metabolizer 2", "Deficiency of nudix hydrolase 15", "THIOPURINES, POOR METABOLISM OF, 2", "Nucleotide diphosphatase deficiency", "Deficiency of nudix hydrolase 15 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 5}
{"curie": "MONDO:0020800", "names": ["demyelinating disorders", "demyelinating CNS disease", "CNS demyelinating disease", "Demyelinating CNS disease", "CNS DEMYELINATING DISEASE", "CNS demyelinating disorder", "demyelinating disorders of CNS", "Demyelinating disease of central nervous system", "demyelinating disease of central nervous system", "Demyelinating Disease of Central Nervous System", "Demyelinating Disorder of Central Nervous System", "demyelinating disorder of central nervous system", "demyelinating disorders of central nervous system", "Demyelinating disease central nervous system (CNS)", "demyelinating disease central nervous system (CNS)", "DEMYELINATING DISEASES OF THE CENTRAL NERVOUS SYSTEM", "Demyelinating disease of central nervous system, NOS", "Demyelinating diseases of the central nervous system", "Demyelinating disorders of the central nervous system", "demyelinating disorders of the central nervous system", "Demyelinating disease of central nervous system (disorder)", "Demyelinating disease of central nervous system, unspecified", "demyelinating disorders of central nervous system (diagnosis)", "disease (or disorder); demyelinating (central nervous system)", "Demyelinating diseases of the central nervous system (G35-G37)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "demyelinating disease of central nervous system", "shortest_name_length": 23}
{"curie": "MONDO:0007750", "names": ["FH", "FHC", "FHCL1", "LDLCQ2", "LDL INC", "LDL raised", "Raised LDL", "ldl raising", "increased ldl", "LDL INCREASED", "Increased LDL", "LDL increased", "Type II lipidemia", "IIa; Frederickson", "Frederickson; IIa", "Type II lipidaemia", "LDL Receptor Disorder", "LDL receptor disorder", "LDL RECEPTOR DISORDER", "Type II Hyperlipidemia", "Type II hyperlipidemia", "LDL Receptor Disorders", "HYPERLIPIDEMIA TYPE II", "Disorder, LDL Receptor", "Receptor Disorder, LDL", "hyperlipidemia type ii", "Type IIa hyperlipidemia", "Type IIa Hyperlipidemia", "Type II hyperlipidaemia", "Receptor Disorders, LDL", "Hyperlipidemia Type IIa", "Disorders, LDL Receptor", "Elevated LDL cholesterol", "ldl cholesterol elevated", "Hyperbetalipoproteinemia", "HYPERBETALIPOPROTEINEMIA", "CHOLESTEROL LDL ELEVATED", "Type IIa hyperlipidaemia", "hyperbetalipoproteinemia", "Hyperbetalipoproteinemias", "LDL cholesterol increased", "Hyperbetalipoproteinaemia", "Increased LDL cholesterol", "Hyper-beta-Lipoproteinemia", "LDL cholesterol level QTL2", "Hyper beta Lipoproteinemia", "Increased beta-lipoproteins", "Hyper-beta-Lipoproteinemias", "Increased plasma LDL levels", "familial hypercholesteremia", "Hyperlipoproteinemia Type 2", "HYPERLIPOPROTEINEMIA TYPE II", "Hyperlipoproteinemia Type II", "Increased LDLc concentration", "Type II hyperlipoproteinemia", "type ii hyperlipoproteinemia", "Type 2, Hyperlipoproteinemia", "hyperlipoproteinemia, type 2", "Hyperlipoproteinemia Type 2s", "Type II Hyperlipoproteinemia", "Hyperlipoproteinemia Type IIs", "Familial hypercholesterolemia", "Type IIa hyperlipoproteinemia", "Type II Hyperlipoproteinemias", "Fredrickson Type II lipidemia", "Hyperlipoproteinemia Type IIa", "Familial Hypercholesterolemia", "hyperlipoproteinemia, type 2A", "HYPERLIPOPROTEINEMIA, TYPE II", "Type IIa Hyperlipoproteinemia", "Hyperlipoproteinemia, Type II", "HYPERLIPOPROTEINEMIA TYPE IIA", "FAMILIAL HYPERCHOLESTEROLEMIA", "familial hypercholesterolemia", "Type II hyperlipoproteinaemia", "Fredrickson Type IIa lipidemia", "hyperlipoproteinemia type II-A", "HYPERLIPOPROTEINEMIA, TYPE IIA", "Familial hypercholesterolaemia", "Hypercholesterolemia, Familial", "Familial Hypercholesterolemias", "Hyperlipoproteinemia, Type IIa", "Fredrickson Type II lipidaemia", "familial hypercholesterolaemia", "Type IIa Hyperlipoproteinemias", "Hyperlipoproteinemia Type IIas", "Hyperlipoproteinemias, Type II", "Type IIa hyperlipoproteinaemia", "essential hypercholesterolemia", "hypercholesterolemia, familial", "Essential Hypercholesterolemia", "Hypercholesterolemia, Essential", "Fredrickson Type IIa lipidaemia", "Hyperlipoproteinemias, Type IIa", "Essential Hypercholesterolemias", "Hypercholesterolemias, Familial", "Increased circulating LDL level", "Hypercholesterolemias, Essential", "FAMILIAL HYPERBETALIPOPROTEINEMIA", "HYPER-LOW-DENSITY-LIPOPROTEINEMIA", "HYPERCHOLESTEROLEMIA, FAMILIAL, 1", "hyper-low-density-lipoproteinemia", "Hyper Low Density Lipoproteinemia", "Hyper-Low Density Lipoproteinemia", "Low density lipoprotein increased", "hypercholesterolemia, familial, 1", "familial hyperbetalipoproteinemia", "Hyper-Low-Density-Lipoproteinemia", "LOW DENSITY LIPOPROTEIN INCREASED", "Familial hyperbetalipoproteinemia", "Hyper-Low-Density-Lipoproteinemias", "Lipoproteinemia, Hyper-Low Density", "Hyper-Low Density Lipoproteinemias", "Familial hyperbetalipoproteinaemia", "Density Lipoproteinemia, Hyper-Low", "Fredrickson Type II hyperlipidemia", "Fredrickson type IIa hyperlipidemia", "Density Lipoproteinemias, Hyper-Low", "Lipoproteinemias, Hyper-Low Density", "Fredrickson Type IIa hyperlipidemia", "Hyperbetalipoproteinemia (disorder)", "Fredrickson Type II hyperlipidaemia", "hyperbetalipoproteinemia (diagnosis)", "Fredrickson Type IIa hyperlipidaemia", "familial hyperlipoproteinemia type II", "Familial hyperlipoproteinemia type IIa", "Autosomal Dominant Hypercholesterolemia", "Increased LDL cholesterol concentration", "hypercholesterolemia, susceptibility to", "Essential familial hypercholesterolemia", "ESSENTIAL FAMILIAL HYPERCHOLESTEROLEMIA", "Familial hyperlipoproteinaemia type IIa", "Familial hypercholesterolemia (disorder)", "Dominant Hypercholesterolemia, Autosomal", "Hypercholesterolemia, Autosomal Dominant", "Low density lipoprotein cholesterol high", "Essential familial hypercholesterolaemia", "HYPERCHOLESTEROLEMIA, ESSENTIAL FAMILIAL", "Autosomal Dominant Hypercholesterolemias", "Low density lipoprotein catabolic defect", "Fredrickson Type IIa hyperlipoproteinemia", "familial hypercholesterolemia (diagnosis)", "Hypercholesterolemias, Autosomal Dominant", "Dominant Hypercholesterolemias, Autosomal", "Fredrickson type IIa hyperlipoproteinemia", "hyperlipoproteinemia; Fredrickson type IIa", "Fredrickson; type IIa hyperlipoproteinemia", "Fredrickson Type IIa hyperlipoproteinaemia", "hyperlipoproteinemia type II-A (diagnosis)", "essential hypercholesterolemia (diagnosis)", "Fredrickson type IIa hyperlipoproteinaemia", "Familial Hypercholesterolemic Xanthomatosis", "Familial Hypercholesterolemic Xanthomatoses", "Hyperlipoproteinemia, Frederickson type IIa", "hypercholesterolemia, familial, modifier of", "Hypercholesterolemic Xanthomatosis, Familial", "Xanthomatoses, Familial Hypercholesterolemic", "Xanthomatosis, Familial Hypercholesterolemic", "Hypercholesterolemic Xanthomatoses, Familial", "HYPERCHOLESTEROLEMIC XANTHOMATOSIS, FAMILIAL", "hypercholesterolemic xanthomatosis, familial", "Fredrickson's hyperlipoproteinemia, type IIa", "Low density lipoprotein cholesterol increased", "LDL - Low density lipoprotein receptor disorder", "Fredrickson type IIa hyperlipidemia (diagnosis)", "Fredrickson type IIa hyperlipoproteinemia (disorder)", "Increased circulating low-density lipoprotein levels", "Increased circulating low-density lipoprotein cholesterol", "hypercholesterolemia, familial, due to ldlr defect, modifier of", "LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 2", "low density lipoprotein cholesterol level quantitative trait locus 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypercholesterolemia, familial, 1", "shortest_name_length": 2}
{"curie": "UMLS:C4727004", "names": ["Locally Advanced Bone Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Bone Sarcoma", "shortest_name_length": 29}
{"curie": "UMLS:C4525893", "names": ["Stage II Pancreatic Neuroendocrine Tumor", "Stage II Pancreatic Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Pancreatic Neuroendocrine Tumor AJCC v8", "shortest_name_length": 40}
{"curie": "MONDO:0012531", "names": ["XPB", "XPBC", "XP-B", "XPB/CS", "XP group B", "XP, GROUP B", "XP, Group B", "ERCC3 xeroderma pigmentosum", "Xeroderma pigmentosum group B", "xeroderma pigmentosum group B", "Xeroderma Pigmentosum Group B", "xeroderma pigmentosum, type 2", "Xeroderma pigmentosum, group B", "xeroderma pigmentosum, group B", "Xeroderma Pigmentosum, Group B", "xeroderma pigmentosum group type B", "Xeroderma pigmentosum, group B (disorder)", "XERODERMA PIGMENTOSUM B/COCKAYNE SYNDROME", "xeroderma pigmentosum B/Cockayne syndrome", "Xeroderma Pigmentosum B-Cockayne Syndrome", "Xeroderma Pigmentosum, Complementation Group B", "xeroderma pigmentosum, complementation group B", "XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B", "xeroderma pigmentosum caused by mutation in ERCC3", "xeroderma pigmentosum, complementation group type B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "xeroderma pigmentosum group B", "shortest_name_length": 3}
{"curie": "MONDO:0100051", "names": ["idiopathic MACS", "idiopathic mast cell activation syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic mast cell activation syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0001526", "names": ["labia minora cancer", "labium minora cancer", "cancer of labium minora", "malignant labia minora tumor", "Malignant Labia Minora Tumor", "Malignant Tumor of Labia Minora", "malignant tumor of Labia Minora", "malignant tumor of labia minora", "malignant labia minora neoplasm", "Malignant Labia Minora Neoplasm", "malignant labium minora neoplasm", "Malignant neoplasm of labium minus", "Malignant Neoplasm of Labia Minora", "malignant neoplasm of labia minora", "malignant neoplasm of labium minus", "Malignant neoplasm of labia minora", "malignant tumor of the labia minora", "Malignant Tumor of the Labia Minora", "malignant neoplasm of labium minora", "Malignant Neoplasm of the Labia Minora", "malignant neoplasm of the labia minora", "Malignant neoplasm of labia minora (disorder)", "malignant neoplasm of labia minora (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "labia minora cancer", "shortest_name_length": 19}
{"curie": "MONDO:0009559", "names": ["Mandibulofacial Dysostosis with Mental Deficiency", "mandibulofacial dysostosis with mental deficiency", "mandibulofacial dysostosis with mental retardation", "MANDIBULOFACIAL DYSOSTOSIS WITH MENTAL RETARDATION", "mandibulofacial dysostosis with intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mandibulofacial dysostosis with mental deficiency", "shortest_name_length": 49}
{"curie": "MONDO:0000849", "names": ["Baker's disease", "baker's disease", "fibrogenesis imperfecta ossium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibrogenesis imperfecta ossium", "shortest_name_length": 15}
{"curie": "UMLS:C1336279", "names": ["Stage II AIDS-Related Anal Canal Cancer", "Stage II AIDS-Related Anal Canal Cancer AJCC v6", "Stage II AIDS-Related Anal Canal Cancer AJCC v7", "Stage II AIDS-Related Anal Carcinoma AJCC v6 and v7", "Stage II AIDS-Related Anal Canal Cancer AJCC v6 and v7", "Stage II AIDS-Related Anal Canal Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II AIDS-Related Anal Canal Cancer AJCC v6 and v7", "shortest_name_length": 39}
{"curie": "MONDO:0025489", "names": ["bovine Leukoses", "bovine leukemia", "Bovine Leukoses", "Bovine leukosis", "bovine lymphoma", "bovine leukosis", "Bovine Leukosis", "lymphoma, bovine", "leukemia, bovine", "leukoses, bovine", "Leukosis, Bovine", "bovine leukemias", "Leukoses, Bovine", "bovine Lymphomas", "leukosis, bovine", "lymphomas, bovine", "leukemias, bovine", "bovine lymphosarcoma", "bovine Lymphosarcomas", "Bovine viral leukosis", "leukosis viral bovine", "lymphosarcoma, bovine", "lymphosarcomas, bovine", "Enzootic bovine leukosis", "enzootic bovine Leukoses", "Enzootic Bovine Leukosis", "Enzootic Bovine Leukoses", "enzootic bovine leukosis", "bovine Leukoses, enzootic", "bovine leukosis, enzootic", "Bovine Leukosis, Enzootic", "Bovine Leukoses, Enzootic", "Leukosis, Enzootic Bovine", "leukosis, enzootic bovine", "leukoses, enzootic bovine", "Leukoses, Enzootic Bovine", "Malignant lymphoma of cattle", "Bovine viral leukosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "enzootic bovine leukosis", "shortest_name_length": 15}
{"curie": "MONDO:0003685", "names": ["Retroperitoneal Germ Cell Tumor", "retroperitoneal germ cell tumor", "germ cell tumor of Retroperitoneum", "germ cell tumor of retroperitoneum", "retroperitoneal germ cell neoplasm", "Retroperitoneal Germ Cell Neoplasm", "Germ Cell Tumor of Retroperitoneum", "germ cell neoplasm of retroperitoneum", "Germ Cell Neoplasm of Retroperitoneum", "Germ Cell Tumor of the Retroperitoneum", "germ cell tumor of the retroperitoneum", "germ cell neoplasm of the retroperitoneum", "Germ Cell Neoplasm of the Retroperitoneum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retroperitoneal germ cell neoplasm", "shortest_name_length": 31}
{"curie": "UMLS:C4524896", "names": ["Stage IIA Anal Cancer", "stage IIA anal cancer", "stage IIA anal cancer AJCC v8", "Stage IIA Anal Cancer AJCC v8", "Stage IIA Anal Carcinoma AJCC v8", "stage IIA anal carcinoma AJCC v8", "stage IIA anal canal and perianal (anal margin) carcinoma AJCC v8", "Stage IIA Anal Canal and Perianal (Anal Margin) Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Anal Cancer AJCC v8", "shortest_name_length": 21}
{"curie": "UMLS:C0010340", "names": ["critically ill", "Critically ill", "Critically Ill", "Critical Illness", "Critical illness", "critical illness", "Illness, Critical", "Critical Illnesses", "Illnesses, Critical"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Critical Illness", "shortest_name_length": 14}
{"curie": "UMLS:C4727412", "names": ["Recurrent Parotid Gland Carcinoma ex Pleomorphic Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Parotid Gland Carcinoma ex Pleomorphic Adenoma", "shortest_name_length": 56}
{"curie": "UMLS:C0004565", "names": ["B16 Melanoma", "B16 Melanomas", "Melanoma, B16", "Melanomas, B16", "B16 Malignant Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Melanoma, B16", "shortest_name_length": 12}
{"curie": "UMLS:C0342124", "names": ["hashitoxicosis", "Hashitoxicosis", "Hashimoto Toxicosis", "Hashimoto; thyrotoxicosis", "Hyperthyroidism with Hashimoto disease", "Hashimoto thyroiditis with hyperthyroidism", "thyrotoxicosis; in Hashimoto's thyroiditis", "Thyrotoxicosis due to Hashimoto's thyroiditis", "Hyperthyroidism with Hashimoto disease (disorder)", "Hashimoto thyroiditis with hyperthyroidism (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyperthyroidism with Hashimoto disease", "shortest_name_length": 14}
{"curie": "MONDO:0018174", "names": ["hereditary glaucoma", "Hereditary glaucoma", "Hereditary Glaucoma", "Early-Onset Glaucoma", "glaucoma, hereditary", "hereditary glaucoma (disease)", "Pediatric-onset glaucoma of genetic origin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary glaucoma", "shortest_name_length": 19}
{"curie": "MONDO:0015208", "names": ["syndromic esophageal malformation", "syndrome associated with esophageal malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic esophageal malformation", "shortest_name_length": 33}
{"curie": "MONDO:0021739", "names": ["prurigo", "Prurigo", "itchy rash", "Itchy rash", "rash itchy", "Prurigo NOS", "Prurigo, NOS", "Pruritic rash", "PRURITIC RASH", "Rash pruritic", "pruritic rash", "Pruritic rash, NOS", "prurigo (diagnosis)", "Itchy skin eruption", "itchy skin eruption", "Itchy skin eruption, NOS", "Pruritic rash (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prurigo", "shortest_name_length": 7}
{"curie": "UMLS:C4527072", "names": ["stage IIIB Merkel cell carcinoma", "Pathologic Stage IIIB Merkel Cell Carcinoma AJCC v8", "pathologic stage IIIB Merkel cell carcinoma AJCC v8", "pathologic stage IIIB neuroendocrine carcinoma of the skin AJCC v8", "Pathologic Stage IIIB Neuroendocrine Carcinoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IIIB Merkel Cell Carcinoma AJCC v8", "shortest_name_length": 32}
{"curie": "MONDO:0032783", "names": ["AOVD3", "BICUSPID AORTIC VALVE", "AORTIC VALVE STENOSIS", "AORTIC VALVE DISEASE 3", "aortic valve disease 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic valve disease 3", "shortest_name_length": 5}
{"curie": "MONDO:0001361", "names": ["ocular nystagmus", "Ocular nystagmus", "Amaurotic nystagmus", "Roving eye movement", "Roving eye movements", "roving eye movements", "searching eye movements", "Searching eye movements", "visual deprivation nystagmus", "spontaneous ocular nystagmus", "Spontaneous ocular nystagmus", "Visual deprivation nystagmus", "Spontaneous Ocular Nystagmus", "Nystagmus, spontaneous ocular", "Nystagmus, Spontaneous Ocular", "Ocular Nystagmus, Spontaneous", "Visual deprivation nystagmus (disorder)", "visual deprivation nystagmus (diagnosis)", "Spontaneous eye movements associated with binocular visual loss"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spontaneous ocular nystagmus", "shortest_name_length": 16}
{"curie": "MONDO:0030809", "names": ["SPGF72", "spermatogenic failure 72", "SPERMATOGENIC FAILURE 72"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 72", "shortest_name_length": 6}
{"curie": "MONDO:0034954", "names": ["syndromic vitreoretinopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic vitreoretinopathy", "shortest_name_length": 27}
{"curie": "UMLS:C0233105", "names": ["Complete abortion", "complete abortion", "Complete Abortion", "Abortion complete", "Abortion, complete", "Abortion complete NOS", "Complete Induced Abortion", "complete abortion (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abortion complete", "shortest_name_length": 17}
{"curie": "UMLS:C2936346", "names": ["22q11 Deletion Syndrome", "22q11 Deletion Syndromes", "Deletion Syndrome, 22q11", "Syndrome, 22q11 Deletion", "Deletion Syndromes, 22q11", "Syndromes, 22q11 Deletion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "22q11 Deletion Syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0002463", "names": ["lacrimal gland carcinoma", "Lacrimal Gland Carcinoma", "Carcinoma of Lacrimal Gland", "carcinoma of lacrimal gland", "carcinoma of the lacrimal gland", "Carcinoma of the Lacrimal Gland", "carcinoma of lacrimal gland (diagnosis)", "lacrimal gland neoplasm malignant carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lacrimal gland carcinoma", "shortest_name_length": 24}
{"curie": "UMLS:C0595861", "names": ["parasuicide", "Parasuicide", "Parasuicides", "Parasuicide (event)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parasuicide", "shortest_name_length": 11}
{"curie": "MONDO:0700087", "names": ["US1", "USH1", "USH1B", "USH1A, FORMERLY", "Usher syndrome type 1", "Usher Syndrome Type 1", "USHER SYNDROME, TYPE I", "Usher Syndrome, Type I", "Usher syndrome type 1B", "USHER SYNDROME, TYPE IB", "Usher syndrome, type 1B", "Usher Syndrome, Type Ib", "Usher syndrome type 1 (disorder)", "Usher syndrome type 1 (diagnosis)", "USHER SYNDROME, TYPE IA, FORMERLY", "Usher syndrome type 1B (diagnosis)", "USHER SYNDROME, TYPE IB (disorder)", "RETINITIS PIGMENTOSA AND CONGENITAL DEAFNESS", "USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Usher syndrome type 1B", "shortest_name_length": 3}
{"curie": "UMLS:C0279975", "names": ["Relapsed Ovarian Germ Cell Tumor", "Recurrent Ovarian Germ Cell Tumor", "recurrent ovarian germ cell tumor", "Relapsed Germ Cell Tumor of Ovary", "Recurrent Germ Cell Tumor of Ovary", "ovarian germ cell tumor, recurrent", "germ cell tumor, ovarian, recurrent", "Relapsed Ovarian Germ Cell Neoplasm", "Recurrent Ovarian Germ Cell Neoplasm", "Relapsed Germ Cell Neoplasm of Ovary", "Recurrent Germ Cell Neoplasm of Ovary", "Relapsed Germ Cell Tumor of the Ovary", "Recurrent Germ Cell Tumor of the Ovary", "Relapsed Germ Cell Neoplasm of the Ovary", "Recurrent Germ Cell Neoplasm of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Ovarian Germ Cell Tumor", "shortest_name_length": 32}
{"curie": "MONDO:0016006", "names": ["Cockayne", "progeroid nanism", "Progeroid Nanism", "Cockayne Syndrome", "syndrome cockayne", "Cockayne syndrome", "cockayne syndrome", "Syndrome, Cockayne", "cockaynes syndrome", "progeroid syndrome", "Progeroid syndrome", "Cockayne syndrome 1", "Cockayne's syndrome", "cockayne's syndrome", "Progeria Like Syndrome", "progeria-like syndrome", "Progeria-Like Syndrome", "Progeria-like syndrome", "Syndrome, Progeria-Like", "Neill-Dingwall syndrome", "Progeria-Like Syndromes", "neill-dingwall syndrome", "Cockayne syndrome (CS) 1", "mulvihill smith syndrome", "Cockayne syndrome (disorder)", "Cockayne syndrome (diagnosis)", "Dwarfism-Retinal Atrophy-Deafness Syndrome", "dwarfism-retinal atrophy-deafness syndrome", "Dwarfism-retinal atrophy-deafness syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cockayne syndrome", "shortest_name_length": 8}
{"curie": "MONDO:0015556", "names": ["nodular urticaria pigmentosa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nodular urticaria pigmentosa", "shortest_name_length": 28}
{"curie": "MONDO:0008380", "names": ["Rb", "RB", "RB1", "Retina tumor", "Retina tumour", "RETINA, GLIOMA", "Retinoblastoma", "retinoblastoma", "RETINOBLASTOMA", "Retinal Glioma", "Glioma, Retinal", "Retinoblastomas", "retinoblastomas", "Retinal Gliomas", "Gliomas, Retinal", "Retinoblastoma NOS", "Retinoblastoma, NOS", "RB - Retinoblastoma", "RB - retinoblastoma", "Retinal Glioblastoma", "Glioblastoma, Retinal", "Retinal Glioblastomas", "Retinal Neuroblastoma", "Glioblastomas, Retinal", "Retinal Neuroblastomas", "Neuroblastoma, Retinal", "Neuroblastomas, Retinal", "neuroblastoma of Retina", "Neuroblastoma of Retina", "disorders retinoblastoma", "Retinoblastoma Eye Cancer", "RETINOBLASTOMA, MALIGNANT", "retinoblastoma, malignant", "Retinoblastoma (disorder)", "Cancer, Retinoblastoma Eye", "Retinoblastoma Eye Cancers", "Eye Cancer, Retinoblastoma", "retinoblastoma (diagnosis)", "eye cancer, retinoblastoma", "Cancers, Retinoblastoma Eye", "Retinoblastoma - morphology", "Eye Cancers, Retinoblastoma", "Neuroblastoma of the Retina", "malignant retinoblastoma of eye", "Retinoblastoma (morphologic abnormality)", "malignant retinoblastoma of eye (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinoblastoma", "shortest_name_length": 2}
{"curie": "MONDO:0010458", "names": ["HYSP4", "hypospadias 4, X-linked", "HYPOSPADIAS 4, X-LINKED, SUSCEPTIBILITY TO", "hypospadias 4, X-linked, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypospadias 4, X-linked", "shortest_name_length": 5}
{"curie": "UMLS:C1336410", "names": ["Stage IV AIDS-Related Anal Canal Cancer", "Stage IV AIDS-Related Anal Canal Cancer AJCC v7", "Stage IV AIDS-Related Anal Canal Cancer AJCC v6", "Stage IV AIDS-Related Anal Carcinoma AJCC v6 and v7", "Stage IV AIDS-Related Anal Canal Cancer AJCC v6 and v7", "Stage IV AIDS-Related Anal Canal Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV AIDS-Related Anal Canal Cancer AJCC v6 and v7", "shortest_name_length": 39}
{"curie": "UMLS:C5671027", "names": ["Supratentorial Ependymoma, NOS", "Supratentorial Ependymoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Supratentorial Ependymoma, Not Otherwise Specified", "shortest_name_length": 30}
{"curie": "MONDO:0001211", "names": ["total internal ophthalmoplegia", "Total internal ophthalmoplegia", "Complete internal ophthalmoplegia", "Internal ophthalmoplegia, complete", "Total internal ophthalmoplegia (disorder)", "total internal ophthalmoplegia (diagnosis)", "Total or complete internal ophthalmoplegia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "total internal ophthalmoplegia", "shortest_name_length": 30}
{"curie": "UMLS:C4763671", "names": ["Vinyl and/or derivatives", "Vinyl Chloride or Derivatives Exposure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vinyl Chloride or Derivatives Exposure", "shortest_name_length": 24}
{"curie": "MONDO:0007773", "names": ["hyperproglucagonemia", "Hyperproglucagonemia", "HYPERPROGLUCAGONEMIA", "GLUCAGON, LARGE MOLECULAR WEIGHT SPECIES OF", "glucagon, large molecular weight species of", "Glucagon, Large Molecular Weight Species Of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperproglucagonemia", "shortest_name_length": 20}
{"curie": "MONDO:0012831", "names": ["IBD13", "Inflammatory Bowel Disease 13", "inflammatory bowel disease 13", "INFLAMMATORY BOWEL DISEASE 13", "ABCB1 inflammatory bowel disease", "inflammatory bowel disease type 13", "inflammatory bowel disease caused by mutation in ABCB1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory bowel disease 13", "shortest_name_length": 5}
{"curie": "MONDO:0004763", "names": ["dissection carotid artery", "Carotid Artery Dissection", "Carotid artery dissection", "carotid artery dissection", "dissection of carotid artery", "Dissection of carotid artery", "Dissection of carotid artery (disorder)", "dissection of carotid artery (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carotid artery dissection", "shortest_name_length": 25}
{"curie": "UMLS:C1336163", "names": ["Stage IIA Lung Adenocarcinoma", "Stage IIA Adenocarcinoma of Lung", "Stage IIA Adenocarcinoma of the Lung", "Stage IIA Lung Adenocarcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Lung Adenocarcinoma AJCC v7", "shortest_name_length": 29}
{"curie": "MONDO:0016437", "names": ["late-onset focal dermal elastosis", "PXE-like late-onset focal dermal elastosis", "pseudoxanthoma-like late-onset focal dermal elastosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "late-onset focal dermal elastosis", "shortest_name_length": 33}
{"curie": "MONDO:0014856", "names": ["COXPD30", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 30", "combined oxidative phosphorylation deficiency 30", "combined oxidative phosphorylation defect type 30", "Combined oxidative phosphorylation defect type 30", "combined oxidative phosphorylation deficiency type 30", "TRMT10C combined oxidative phosphorylation deficiency", "COXPD30 - combined oxidative phosphorylation defect type 30", "Combined oxidative phosphorylation defect type 30 (disorder)", "combined oxidative phosphorylation deficiency caused by mutation in TRMT10C"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation defect type 30", "shortest_name_length": 7}
{"curie": "MONDO:0027069", "names": ["MC5DM1", "Mitochondrial Complex V Deficiency, Mitochondrial Type 1", "mitochondrial complex V (ATP synthase) deficiency mitochondrial type 1", "mitochondrial complex V (ATP synthase) deficiency, mitochondrial type 1", "MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, MITOCHONDRIAL TYPE 1", "Mitochondrial Complex V (ATP synthase) Deficiency, Mitochondrial Type 1", "mitochondrial complex 5 (ATP synthase) deficiency, mitochondrial type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 5 (ATP synthase) deficiency, mitochondrial type 1", "shortest_name_length": 6}
{"curie": "MONDO:0012177", "names": ["PCARP", "AXPC1", "Pcarp", "POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA", "Posterior column ataxia with retinitis pigmentosa", "POSTERIOR column ataxia with retinitis pigmentosa", "ataxia, posterior column, with retinitis pigmentosa", "posterior column ataxia-retinitis pigmentosa syndrome", "Posterior column ataxia-retinitis pigmentosa syndrome", "Posterior column ataxia with retinitis pigmentosa syndrome", "autosomal recessive posterior column ataxia and retinitis pigmentosa", "Autosomal recessive posterior column ataxia and retinitis pigmentosa", "Autosomal recessive posterior column ataxia and retinitis pigmentosa (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "posterior column ataxia-retinitis pigmentosa syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0007321", "names": ["chondrodysplasia punctata Sheffield type", "chondrodysplasia punctata, Sheffield type", "autosomal dominant chondrodysplasia punctata", "chondrodysplasia punctata, autosomal dominant", "Chondrodysplasia Punctata, Autosomal Dominant", "Chondrodysplasia punctata, autosomal dominant", "CHONDRODYSPLASIA PUNCTATA, AUTOSOMAL DOMINANT", "Chondrodysplasia Punctata Due To Vitamin K Deficiency", "CHONDRODYSPLASIA PUNCTATA DUE TO VITAMIN K DEFICIENCY", "chondrodysplasia punctata due to vitamin K deficiency", "chondrodysplasia punctata due to warfarin teratogenicity", "Chondrodysplasia Punctata Due To Warfarin Teratogenicity", "CHONDRODYSPLASIA PUNCTATA DUE TO WARFARIN TERATOGENICITY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant chondrodysplasia punctata", "shortest_name_length": 40}
{"curie": "UMLS:C5239074", "names": ["Advanced Epithelioid Hemangioendothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Epithelioid Hemangioendothelioma", "shortest_name_length": 41}
{"curie": "UMLS:C0013170", "names": ["Drug habit", "DRUG HABIT", "habituation", "HABITUATION", "Habituation", "DRUG HABITUATING", "Drug habituating", "drug habituation", "Drug Habituation", "Drug habituation", "Habituation, Drug", "Drug habituation (disorder)", "Drug habituation (diagnosis)", "substance abuse drug habituation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drug habituation", "shortest_name_length": 10}
{"curie": "UMLS:C5205734", "names": ["Metastatic Colorectal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Colorectal Adenocarcinoma", "shortest_name_length": 36}
{"curie": "MONDO:0019269", "names": ["DOC", "ICTHYOSIS", "icthyosis", "ichthyosis", "Ichthyosis", "ICHTHYOSIS", "Ichthyoses", "ichthyoses", "Ichthyosis, NOS", "Ichthyotic skin", "fish skin disease", "Fish scale disease", "fish scale disease", "ichthyosis (disease)", "Ichthyosis (disorder)", "ichthyosis (diagnosis)", "Hypertrophic ichthyosis", "non-syndromic ichthyosis", "disorder of cornification", "Skin change ichthyosiform", "Ichthyosiform abnormality of the skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ichthyosis", "shortest_name_length": 3}
{"curie": "MONDO:0015873", "names": ["PD", "Paget; nipple", "nipple; Paget", "Nipple Paget Disease", "mammary Paget disease", "PAGET DISEASE, NIPPLE", "Mammary Paget disease", "Nipple Paget's Disease", "nipple Paget's disease", "Paget disease of nipple", "nipple; disorder, Paget", "Paget's disease, mammary", "Paget's Disease of Nipple", "Paget's disease of nipple", "Paget disease of the nipple", "Paget disease of the breast", "Paget Disease of the Nipple", "Paget's disease of the nipple", "Paget's Disease of the Nipple", "Paget's carcinoma of the nipple", "disease (or disorder); nipple, Paget", "Paget's disease of nipple (disorder)", "Paget's disease of nipple (diagnosis)", "breast neoplasm malignant Paget's disease nipple"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paget disease of the nipple", "shortest_name_length": 2}
{"curie": "MONDO:0006974", "names": ["Round cell tumor", "Small cell sarcoma", "Small Cell Sarcoma", "round cell sarcoma", "small cell sarcoma", "Round cell sarcoma", "Sarcoma, Small Cell", "round cell; sarcoma", "Small Cell Sarcomas", "small cell; sarcoma", "sarcoma; round cell", "sarcoma; small cell", "Cell Sarcoma, Small", "small cell sarcomas", "Cell Sarcomas, Small", "Sarcomas, Small Cell", "Round cell tumor (disorder)", "small cell sarcoma (diagnosis)", "Undifferentiated Round Cell Sarcoma", "Undifferentiated round cell sarcoma", "Small cell sarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small cell sarcoma", "shortest_name_length": 16}
{"curie": "UMLS:C0751590", "names": ["Primary Supratentorial Neoplasm", "Primary Supratentorial Neoplasms", "Neoplasm, Primary Supratentorial", "Supratentorial Neoplasm, Primary", "Neoplasms, Primary Supratentorial", "Supratentorial Neoplasms, Primary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Supratentorial Neoplasms", "shortest_name_length": 31}
{"curie": "MONDO:0005308", "names": ["ciliopathy", "ciliopathies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ciliopathy", "shortest_name_length": 10}
{"curie": "UMLS:C0434014", "names": ["diaphragm injury", "diaphragm; injury", "injury; diaphragm", "Injury of diaphragm", "injury of diaphragm", "Injury to Diaphragm", "Diaphragmatic injury", "diaphragmatic injury", "Injury of diaphragm (disorder)", "injury of diaphragm (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of diaphragm", "shortest_name_length": 16}
{"curie": "MONDO:0019660", "names": ["Pfeiffer syndrome type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pfeiffer syndrome type 2", "shortest_name_length": 24}
{"curie": "UMLS:C0752335", "names": ["Neuropsychiatric lupus", "Neuropsychiatric Systemic Lupus Erythematosus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neuropsychiatric Systemic Lupus Erythematosus", "shortest_name_length": 22}
{"curie": "UMLS:C2981251", "names": ["Stage IVA Sinonasal Cancer AJCC v7", "Stage IVA Sinonasal Carcinoma AJCC v7", "Stage IVA Nasal Cavity and Paranasal Sinus Cancer", "Stage IVA Nasal Cavity and Paranasal Sinus Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Nasal Cavity and Paranasal Sinus Cancer AJCC v7", "shortest_name_length": 34}
{"curie": "UMLS:C1336248", "names": ["Stage III Hepatocellular Cancer", "Stage III Liver Cell Cancer AJCC v6", "Liver Cell Cancer Stage III AJCC v6", "Stage III Hepatocellular Cancer AJCC v6", "Hepatocellular Cancer Stage III AJCC v6", "Stage III Carcinoma of Liver Cells AJCC v6", "Stage III Hepatocellular Carcinoma AJCC v6", "Stage III Carcinoma of the Liver Cells AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Hepatocellular Carcinoma AJCC v6", "shortest_name_length": 31}
{"curie": "UMLS:C1096359", "names": ["VERTEBRA OSTEOPHYTE", "Vertebral osteophyte", "Osteophyte, vertebrae", "Bone spur of vertebra", "Osteophyte of vertebra", "osteophyte of vertebrae", "Osteophyte of vertebra (disorder)", "osteophyte of vertebrae (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone spur of vertebra", "shortest_name_length": 19}
{"curie": "UMLS:C0149844", "names": ["brain contusion", "Brain contusion", "contusion brain", "Brain Contusion", "brain contusions", "brain; contusion", "BRAIN, CONTUSION", "Brain Contusions", "Contusion, Brain", "Contusio Cerebri", "contusion; brain", "Contusions, Brain", "contusion of brain", "Contusion of brain", "of brain contusion", "Contusion of brain, NOS", "Contusional brain injury", "Contusion of brain (disorder)", "Contusion of brain (diagnosis)", "head injury contusion of brain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brain Contusion", "shortest_name_length": 15}
{"curie": "UMLS:C4528569", "names": ["Breast Cancer by AJCC v8 Prognostic Stage", "Breast Carcinoma by AJCC v8 Prognostic Stage", "Breast Cancer by AJCC v8 Prognostic Stage Group"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Cancer by AJCC v8 Prognostic Stage", "shortest_name_length": 41}
{"curie": "MONDO:0010997", "names": ["PSP", "PSNP1", "Richardson syndrome", "classic PSP syndrome", "supranuclear palsy, progressive", "Progressive Supranuclear Palsy 1", "Supranuclear Palsy, Progressive, 1", "supranuclear palsy, progressive, 1", "SUPRANUCLEAR PALSY, PROGRESSIVE, 1", "Steele-Richardson-Olszewski disease", "Steele-Richardson-Olszewski syndrome", "supranuclear palsy, progressive, type 1", "classic progressive supranuclear palsy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "supranuclear palsy, progressive, 1", "shortest_name_length": 3}
{"curie": "MONDO:0005715", "names": ["Toxoplasma embryopathy", "Toxoplasmosis - congen.", "toxoplasmosis - congen.", "Congenital Toxoplasmoses", "toxoplasmosis congenital", "congenital toxoplasmosis", "Toxoplasmosis;congenital", "Congenital Toxoplasmosis", "Congenital toxoplasmosis", "congenital; toxoplasmosis", "Toxoplasmosis, Congenital", "toxoplasmosis; congenital", "toxoplasmosis, congenital", "Toxoplasmoses, Congenital", "TOXOPLASMOSIS, CONGENITAL", "Toxoplasma embryofetopathy", "Congenital Toxoplasma Infection", "Infection, Congenital Toxoplasma", "Congenital Toxoplasma Infections", "Toxoplasma Infection, Congenital", "Infections, Congenital Toxoplasma", "Toxoplasma Infections, Congenital", "Congenital toxoplasmosis (disorder)", "congenital toxoplasmosis (diagnosis)", "Congenital Toxoplasma gondii Infection", "Congenital Infection, Toxoplasma gondii", "mother-to-child transmission of toxoplasmosis", "Mother-to-child transmission of toxoplasmosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital toxoplasmosis", "shortest_name_length": 22}
{"curie": "UMLS:C4525202", "names": ["IB", "Stage IB Hepatocellular Cancer", "Stage IB Liver Cell Carcinoma AJCC v8", "Stage IB Hepatocellular Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Hepatocellular Carcinoma AJCC v8", "shortest_name_length": 2}
{"curie": "MONDO:0009020", "names": ["MCD", "Mcd", "Mcdc1", "Mcdc1, formerly", "MCDC1, FORMERLY", "Fehr corneal dystrophy", "macular corneal dystrophy", "Corneal Macular Dystrophy", "Macular corneal dystrophy", "corneal macular dystrophy", "Macular Corneal Dystrophy", "Dystrophy, Corneal Macular", "MACULAR DYSTROPHY, CORNEAL", "Macular Dystrophy, Corneal", "macular dystrophy, corneal", "Dystrophy, macular corneal", "Macular dystrophy of cornea", "Corneal Macular Dystrophies", "Macular Dystrophy, Corneal, 1", "macular dystrophy, corneal, 1", "MACULAR DYSTROPHY, CORNEAL, 1", "Corneal dystrophy, macular type", "CORNEAL DYSTROPHY, MACULAR TYPE", "corneal dystrophy, macular type", "Macular corneal dystrophy Type I", "Macular corneal dystrophy type 1", "macular corneal dystrophy type 1", "Macular Corneal Dystrophy, Type I", "macular corneal dystrophy, type I", "Macular dystrophy, corneal type 1", "Groenouw type 2 corneal dystrophy", "macular corneal dystrophy, type 1", "Macular corneal dystrophy Type II", "MACULAR CORNEAL DYSTROPHY, TYPE I", "macular dystrophy, corneal type 1", "macular corneal dystrophy, type 2", "macular corneal dystrophy, type II", "Corneal dystrophy Groenouw type II", "Macular Corneal Dystrophy, Type II", "Groenouw type II corneal dystrophy", "corneal dystrophy Groenouw type II", "GROENOUW TYPE II CORNEAL DYSTROPHY", "MACULAR CORNEAL DYSTROPHY, TYPE II", "Macular corneal dystrophy (disorder)", "macular corneal dystrophy (diagnosis)", "Macular corneal dystrophy Type I (disorder)", "Macular corneal dystrophy Type II (disorder)", "macular corneal dystrophy, type I (diagnosis)", "macular corneal dystrophy, type II (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macular corneal dystrophy", "shortest_name_length": 3}
{"curie": "MONDO:0002156", "names": ["Salpingopathy", "Fallopian Tube Disease", "fallopian tube disease", "Fallopian tube disease", "fallopian tube disorder", "Fallopian Tube Diseases", "diseases fallopian tube", "fallopian tube diseases", "Fallopian Tube Disorder", "Disease, Fallopian Tube", "Fallopian tube disorder", "Diseases, Fallopian Tube", "disorders fallopian tube", "fallopian tube disorders", "disorders fallopian tubes", "Fallopian tubes--Diseases", "disease of fallopian tube", "disorder of fallopian tube", "Disorder of fallopian tube", "fallopian tube disease or disorder", "Fallopian tube disorder (disorder)", "fallopian tube disorders (diagnosis)", "disease or disorder of fallopian tube", "disease (or disorder); fallopian tube, tubal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fallopian tube disorder", "shortest_name_length": 13}
{"curie": "MONDO:0003313", "names": ["vaginal endometrial stromal sarcoma", "vagina endometrioid stromal sarcoma", "endometrioid stromal sarcoma of vagina", "endometrioid stromal sarcoma of the vagina", "Endometrioid Stromal Sarcoma of the Vagina"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometrioid stromal sarcoma of the vagina", "shortest_name_length": 35}
{"curie": "MONDO:0019022", "names": ["sensorineural hearing loss-early graying-essential tremor syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sensorineural hearing loss-early graying-essential tremor syndrome", "shortest_name_length": 66}
{"curie": "MONDO:0015289", "names": ["infectious epithelial keratitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infectious epithelial keratitis", "shortest_name_length": 31}
{"curie": "UMLS:C4521632", "names": ["Stage III Laryngeal Throat Cancer", "Stage III Laryngeal Cancer AJCC v8", "Stage III Laryngeal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Laryngeal Cancer AJCC v8", "shortest_name_length": 33}
{"curie": "MONDO:0700009", "names": ["chromosome 2 disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 2 disorder", "shortest_name_length": 21}
{"curie": "MONDO:0016009", "names": ["German syndrome", "Tridione syndrome", "tridione syndrome", "trimethadione syndrome", "paramethadione syndrome", "Trimethadione embryopathy", "trimethadione embryopathy", "Fetal trimethadione syndrome", "fetal trimethadione syndrome", "Foetal trimethadione syndrome", "Fetal trimethadione syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fetal trimethadione syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0004766", "names": ["Asthmatic Shock", "Asthmatic Crises", "asthmatic crisis", "Asthmatic Shocks", "Asthmatic Crisis", "Asthmatic crisis", "Shock, Asthmatic", "Crises, Asthmatic", "Shocks, Asthmatic", "Crisis, Asthmatic", "status asthmaticus", "STATUS ASTHMATICUS", "Status asthmaticus", "Status Asthmaticus", "asthmaticus status", "acute severe asthma", "Asthmaticus, Status", "severe acute asthma", "Acute severe asthma", "status; asthmaticus", "asthmaticus; status", "severe asthma attack", "Severe asthma attack", "asthma asthmaticus status", "asthma with status asthmaticus", "ASTHMA WITH STATUS ASTHMATICUS", "Asthma with status asthmaticus", "Acute severe exacerbation of asthma", "asthma with acute exacerbation severe", "asthma with acute severe exacerbation", "asthma with status asthmaticus (diagnosis)", "Acute severe exacerbation of asthma (disorder)", "Asthma, unspecified type, with status asthmaticus", "asthma with acute severe exacerbation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "status asthmaticus", "shortest_name_length": 15}
{"curie": "MONDO:0009003", "names": ["ACHM2", "RMCH2", "Monochromacy", "achromatopsia 2", "Achromatopsia 2", "ACHROMATOPSIA 2", "Rod monochromacy 2", "ROD MONOCHROMACY 2", "Rod monochromatism", "rod monochromacy 2", "CNGA3 achromatopsia", "Total colorblindness", "ROD MONOCHROMATISM 2", "achromatopsia type 2", "Rod monochromatism 2", "rod monochromatism 2", "Colorblindness, Total", "Blindness color total", "Total color blindness", "COLORBLINDNESS, TOTAL", "colorblindness, total", "Total colour blindness", "Complete achromatopsia", "Complete color blindness", "Complete colour blindness", "Complete achromatopsia (disorder)", "achromatopsia caused by mutation in CNGA3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "achromatopsia 2", "shortest_name_length": 5}
{"curie": "MONDO:0030486", "names": ["DYT32", "dystonia 32", "DYSTONIA 32"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dystonia 32", "shortest_name_length": 5}
{"curie": "MONDO:0011893", "names": ["DFNA42", "DFNA52", "autosomal dominant deafness 52", "deafness, autosomal dominant 42", "deafness, autosomal dominant 52", "Deafness, Autosomal Dominant 52", "DEAFNESS, AUTOSOMAL DOMINANT 42", "DEAFNESS, AUTOSOMAL DOMINANT 52", "autosomal dominant nonsyndromic deafness 52", "autosomal dominant nonsyndromic hearing loss 52", "autosomal dominant nonsyndromic deafness type 52"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 52", "shortest_name_length": 6}
{"curie": "MONDO:0019553", "names": ["Lipoatrophy due to injected drug", "Drug-induced localised lipoatrophy", "Drug-induced localized lipoatrophy", "lipoatrophy caused by injected drug", "Lipoatrophy caused by injected drug", "drug-induced localized lipodystrophy", "Drug-induced localized lipodystrophy", "Lipoatrophy caused by injected drug (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "drug-induced localized lipodystrophy", "shortest_name_length": 32}
{"curie": "MONDO:0012553", "names": ["COFS2", "ERCC2 COFS syndrome", "cerebrooculofacioskeletal syndrome 2", "CEREBROOCULOFACIOSKELETAL SYNDROME 2", "Cerebrooculofacioskeletal Syndrome 2", "COFS syndrome caused by mutation in ERCC2", "cerebrooculofacioskeletal syndrome type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebrooculofacioskeletal syndrome 2", "shortest_name_length": 5}
{"curie": "MONDO:0006925", "names": ["Fusobacteriaceae Infection", "Fusobacteriaceae infection", "infection, Fusobacteriaceae", "Infection, Fusobacteriaceae", "Fusobacteriaceae Infections", "Infections, Fusobacteriaceae", "infections, Fusobacteriaceae", "Fusobacteriaceae infectious disease", "Fusobacteriaceae disease or disorder", "Fusobacteriaceae caused disease or disorder", "primary Fusobacteriaceae infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fusobacteriaceae infectious disease", "shortest_name_length": 26}
{"curie": "MONDO:0030701", "names": ["autoimmune cardiomyopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune cardiomyopathy", "shortest_name_length": 25}
{"curie": "MONDO:0013959", "names": ["CMT4F", "Charcot-Marie-Tooth disease type 4F", "Charcot-Marie-Tooth disease Type 4F", "CHARCOT-MARIE-TOOTH DISEASE, TYPE 4F", "Charcot-Marie-Tooth disease, type 4F", "PRX Charcot-Marie-Tooth disease type 4", "Prx Charcot-Marie-Tooth disease type 4", "Charcot-Marie-Tooth disease type 4F (disorder)", "Charcot-Marie-Tooth disease Type 4F (diagnosis)", "Charcot-Marie-Tooth disease type 4f (diagnosis)", "Charcot-Marie-Tooth disease, demyelinating, type 4F", "CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 4F", "Charcot-Marie-Tooth disease type 4 caused by mutation in Prx", "Charcot-Marie-Tooth disease type 4 caused by mutation in PRX"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 4F", "shortest_name_length": 5}
{"curie": "MONDO:0016798", "names": ["SANDO", "Ataxia neuropathy spectrum", "ataxia neuropathy spectrum", "Ataxia Neuropathy Spectrum", "Sensory Ataxia Neuropathy Dysarthria and Ophthalmoplegia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ataxia neuropathy spectrum", "shortest_name_length": 5}
{"curie": "MONDO:0012447", "names": ["SD2c", "SPD3", "SPD, Malik type", "SD2, Malik type", "Synpolydactyly 3", "SYNPOLYDACTYLY 3", "synpolydactyly 3", "synpolydactyly type 3", "Synpolydactyly type 3", "Synpolydactyly, Malik type", "synpolydactyly, Malik type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "synpolydactyly type 3", "shortest_name_length": 4}
{"curie": "UMLS:C1336068", "names": ["Splenic Manifestation of T-Cell Prolymphocytic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Splenic Manifestation of T-Cell Prolymphocytic Leukemia", "shortest_name_length": 55}
{"curie": "MONDO:0005175", "names": ["aggressive insulitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aggressive insulitis", "shortest_name_length": 20}
{"curie": "MONDO:0012438", "names": ["PCH5", "Pontocerebellar hypoplasia type 5", "Pontocerebellar Hypoplasia Type 5", "pontocerebellar hypoplasia type 5", "Pontocerebellar hypoplasia, type 5", "PONTOCEREBELLAR HYPOPLASIA, TYPE 5", "pontocerebellar hypoplasia, type 5", "PCH5 - pontocerebellar hypoplasia type 5", "fetal-onset olivopontocerebellar hypoplasia", "Fetal onset olivopontocerebellar hypoplasia", "olivopontocerebellar hypoplasia fetal-onset", "Congenital pontocerebellar hypoplasia type 5", "olivopontocerebellar hypoplasia, fetal-onset", "Olivopontocerebellar hypoplasia, fetal-onset", "OLIVOPONTOCEREBELLAR HYPOPLASIA, FETAL-ONSET", "Foetal onset olivopontocerebellar hypoplasia", "Congenital pontocerebellar hypoplasia type 5 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pontocerebellar hypoplasia type 5", "shortest_name_length": 4}
{"curie": "MONDO:0005505", "names": ["DNT", "DNET", "Dysembryoplastic neurepithelial tumor", "dysembryoplastic neuroepithelial tumor", "Dysembryoplastic Neuroepithelial Tumor", "Dysembryoplastic neuroepithelial tumor", "dysembryoplastic neuroepithelial tumour", "Dysembryoplastic neuroepithelial tumour", "dysembryoplastic neuroepithelial neoplasm", "Dysembryoplastic Neuroepithelial neoplasm", "Dysembryoplastic Neuroepithelial Neoplasm", "Dysembryoplastic neuroepithelial tumor (disorder)", "Dysembryoplastic neuroepithelial tumor (morphologic abnormality)", "dysembryoplastic neuroepithelial tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dysembryoplastic neuroepithelial tumor", "shortest_name_length": 3}
{"curie": "UMLS:C5237382", "names": ["Advanced Breast Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Breast Adenocarcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0009951", "names": ["Radiculoneuropathy, fatal neonatal", "radiculoneuropathy, fatal neonatal", "RADICULONEUROPATHY, FATAL NEONATAL", "Radiculoneuropathy, Fatal Neonatal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radiculoneuropathy, fatal neonatal", "shortest_name_length": 34}
{"curie": "UMLS:C0521757", "names": ["Conjugate Nystagmus", "Conjugate nystagmus", "nystagmus conjugate", "Nystagmus, Conjugate", "Conjugate nystagmus (disorder)", "Conjugate nystagmus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conjugate Nystagmus", "shortest_name_length": 19}
{"curie": "MONDO:0011350", "names": ["DFNA17", "COCHLEOSACCULAR DEGENERATION", "cochleosaccular degeneration", "autosomal dominant deafness 17", "deafness, autosomal dominant 17", "Deafness, Autosomal Dominant 17", "DEAFNESS, AUTOSOMAL DOMINANT 17", "deafness, autosomal dominant type 17", "nonsyndromic hereditary deafness DFNA17", "autosomal dominant nonsyndromic deafness 17", "MYH9 autosomal dominant nonsyndromic deafness", "autosomal dominant nonsyndromic hearing loss 17", "autosomal dominant nonsyndromic deafness type 17", "deafness, autosomal dominant nonsyndromic sensorineural 17", "autosomal dominant nonsyndromic deafness caused by mutation in MYH9", "late-onset progressive hereditary hearing impairment due to cochleosaccular degeneration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 17", "shortest_name_length": 6}
{"curie": "UMLS:C1334731", "names": ["Metastasis to the Nasopharynx", "nasopharyngeal neoplasm metastatic", "Metastatic Tumor to the Nasopharynx", "Metastatic Neoplasm to the Nasopharynx", "Secondary malignant neoplasm of nasopharynx", "Metastatic malignant neoplasm to nasopharynx", "Metastatic Malignant Neoplasm in the Nasopharynx", "Metastatic Malignant Neoplasm to the Nasopharynx", "Secondary malignant neoplasm of nasopharynx, NOS", "Metastatic malignant neoplasm to nasopharynx, NOS", "Metastatic malignant neoplasm to nasopharynx (disorder)", "Metastatic malignant neoplasm to nasopharynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to nasopharynx", "shortest_name_length": 29}
{"curie": "MONDO:0011012", "names": ["BANTU SIDEROSIS", "Bantu siderosis", "African iron overload", "AFRICAN IRON OVERLOAD", "Iron overload in Africa", "iron overload in Africa", "IRON OVERLOAD IN AFRICA", "African nutritional hemochromatosis", "African nutritional haemochromatosis", "hereditary iron overload and African Americans", "African nutritional hemochromatosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "African iron overload", "shortest_name_length": 15}
{"curie": "MONDO:0009291", "names": ["GSD3", "GSDIII", "Forbes", "GSD III", "GSD IIIb", "GSD IIId", "GSD IIID", "GSD IIIa", "GSD IIIA", "GSD IIIB", "GSD type 3", "CORI DISEASE", "cori disease", "Cori Disease", "Cori disease", "Coris Disease", "Disease, Cori", "Cori's disease", "GDE deficiency", "Cori's Disease", "forbes disease", "Agl deficiency", "Gde deficiency", "GDE DEFICIENCY", "Forbes disease", "FORBES DISEASE", "AGL DEFICIENCY", "Glycogenosis 3", "cori's disease", "Forbes Disease", "Forbes' disease", "Disease, Forbes", "forbes' disease", "Glycogenosis 3s", "Disease, Cori's", "limit dextrinosis", "LIMIT DEXTRINOSIS", "Limit Dextrinoses", "Limit Dextrinosis", "Limit dextrinosis", "Dextrinosis, Limit", "Dextrinoses, Limit", "dextrinosis; limit", "glycogenosis type 3", "Glycogenosis type 3", "Cori-Forbes disease", "GLYCOGENOSIS TYPE III", "deficiency of dextrin", "DEBRANCHER DEFICIENCY", "debrancher deficiency", "glycogenosis type III", "Glycogenosis type III", "Debrancher Deficiency", "Debrancher deficiency", "CORI DISEASE, TYPE III", "Deficiency, Debrancher", "Debrancher Deficiencies", "Limit dextrin - glycogen", "Deficiencies, Debrancher", "Glycogen storage disease 3", "glycogen storage disease 3", "Cori disease (GSD type III)", "AGL glycogen storage disease", "debrancher enzyme deficiency", "Debrancher enzyme deficiency", "DEBRANCHER ENZYME DEFICIENCY", "glycogen storage disease iii", "Glycogen Storage Disease III", "GLYCOGEN STORAGE DISEASE III", "glycogen storage disease III", "GLYCOGEN STORAGE DISEASE IIId", "glycogen storage disease IIID", "deficiency; debrancher enzyme", "debrancher enzyme; deficiency", "Glycogen Storage Disease IIIB", "Glycogen Storage Disease IIID", "glycogen storage disease IIIb", "Glycogen Storage Disease IIIA", "glycogen storage disease IIIC", "glycogen storage disease IIIa", "GLYCOGEN STORAGE DISEASE IIIa", "GLYCOGEN STORAGE DISEASE IIIb", "Glycogen Debrancher Deficiency", "GLYCOGEN DEBRANCHER DEFICIENCY", "glycogen Debrancher deficiency", "Debrancher Deficiency, Glycogen", "Deficiency, Glycogen Debrancher", "Glycogen storage disease type 3", "Glycogen Storage Disease Type 3", "glycogen storage disease type 3", "Amylo 1,6 Glucosidase Deficiency", "amylo 1,6 glucosidase deficiency", "amylo-1,6-glucosidase deficiency", "Amylo-1,6-glucosidase deficiency", "Amylo-1,6-Glucosidase Deficiency", "Glycogen Debrancher Deficiencies", "deficiency of debranching enzyme", "AMYLO-1,6-GLUCOSIDASE DEFICIENCY", "GLYCOGEN STORAGE DISEASE TYPE III", "Glycogen storage disease type III", "glycogen storage disease type III", "Deficiency, Amylo-1,6-Glucosidase", "Glycogen Storage Disease Type III", "Debrancher Deficiencies, Glycogen", "Deficiencies, Glycogen Debrancher", "Type III glycogen storage disease", "Amylo-1,6-Glucosidase Deficiencies", "glycogen storage disease, type III", "Glycogen storage disease, type III", "debrancher glycogen storage disease", "Deficiencies, Amylo-1,6-Glucosidase", "Debrancher glycogen storage disease", "Glycogen Debranching Enzyme Deficiency", "Cori disease (GSD type III) (diagnosis)", "Glycogen storage disease, type III (disorder)", "Debrancher deficiency glycogen storage disease", "GSD due to glycogen debranching enzyme deficiency", "glycogen storage disease caused by mutation in AGL", "glycogenosis due to glycogen debranching enzyme deficiency", "Glycogenosis due to glycogen debranching enzyme deficiency", "Glycogen storage disease due to glycogen debranching enzyme deficiency", "glycogen storage disease due to glycogen debranching enzyme deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease III", "shortest_name_length": 4}
{"curie": "UMLS:C4553697", "names": ["Stage IIIC1 Uterine Corpus Cancer AJCC v8", "Stage IIIC1 Uterine (including Endometrial) Cancer", "Stage IIIC1 Uterine Corpus Carcinoma or Carcinosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC1 Uterine Corpus Cancer AJCC v8", "shortest_name_length": 41}
{"curie": "MONDO:0032865", "names": ["PFBMFT5", "PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 5", "pulmonary fibrosis and/or bone marrow failure, telomere-related, 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary fibrosis and/or bone marrow failure, telomere-related, 5", "shortest_name_length": 7}
{"curie": "UMLS:C4744760", "names": ["Thyroid Gland Leiomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Leiomyosarcoma", "shortest_name_length": 28}
{"curie": "UMLS:C4553237", "names": ["Stage II Ovarian Cancer", "Stage II Ovarian Cancer AJCC v8", "Stage II Ovarian Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Ovarian Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "MONDO:0022633", "names": ["Camptodactyly joint contractures and facial skeletal dysplasia", "camptodactyly joint contractures and facial skeletal dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "camptodactyly joint contractures and facial skeletal dysplasia", "shortest_name_length": 62}
{"curie": "MONDO:0030992", "names": ["SOFM", "short stature, oligodontia, dysmorphic facies, and motor delay", "SHORT STATURE, OLIGODONTIA, DYSMORPHIC FACIES, AND MOTOR DELAY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short stature, oligodontia, dysmorphic facies, and motor delay", "shortest_name_length": 4}
{"curie": "MONDO:0009462", "names": ["inosine phosphorylase deficiency, immune defect due to", "INOSINE PHOSPHORYLASE DEFICIENCY, IMMUNE DEFECT DUE TO", "Inosine Phosphorylase Deficiency, Immune Defect Due To"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inosine phosphorylase deficiency, immune defect due to", "shortest_name_length": 54}
{"curie": "MONDO:0016155", "names": ["secondary dystroglycanopathy", "secondary alpha-dystroglycanopathy", "qualitative or quantitative defects of protein involved in O-glycosylation of alpha-dystroglycan"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of protein involved in O-glycosylation of alpha-dystroglycan", "shortest_name_length": 28}
{"curie": "MONDO:0020415", "names": ["Aortic diverticulum", "Kommerell diverticulum", "Kommerells diverticulum", "Kommerell's diverticulum", "Diverticulum of Kommerell", "thoracic aorta diverticulum", "Thoracic aorta diverticulum", "Kommerell's diverticulum (disorder)", "thoracic aorta diverticulum (diagnosis)", "Left aortic arch with retroesophageal diverticulum of Kommerell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kommerell diverticulum", "shortest_name_length": 19}
{"curie": "MONDO:0002681", "names": ["choroid plexus cancer", "tumor of choroid plexus", "choroid plexus neoplasm", "cancer of choroid plexus", "tumor of the Choroid Plexus", "malignant choroid plexus tumor", "Malignant Choroid Plexus Tumor", "malignant choroid plexus tumors", "Malignant Choroid Plexus Tumors", "malignant choroid plexus neoplasm", "Malignant Choroid Plexus Neoplasm", "Malignant Tumor of Choroid Plexus", "malignant tumor of choroid plexus", "malignant choroid plexus neoplasms", "Malignant Choroid Plexus Neoplasms", "malignant neoplasm of choroid plexus", "Malignant Neoplasm of Choroid Plexus", "Malignant Tumor of the Choroid Plexus", "malignant tumor of the choroid plexus", "malignant neoplasm of the choroid plexus", "Malignant Neoplasm of the Choroid Plexus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choroid plexus cancer", "shortest_name_length": 21}
{"curie": "UMLS:C0752334", "names": ["Lupus Meningoencephalitis", "Meningoencephalitis, Lupus", "Lupus Meningoencephalitides", "Meningoencephalitides, Lupus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lupus Meningoencephalitis", "shortest_name_length": 25}
{"curie": "MONDO:0005507", "names": ["cancer gum", "gum cancer", "cancer gums", "cancer of gum", "of gum cancer", "Cancer of gum", "gingiva cancer", "gingival cancer", "GINGIVAL CANCER", "Gingival cancer", "cancer of gingiva", "CA - Cancer of gum", "Malignant Gum Tumor", "malignant gum tumor", "Malignant Gum Neoplasm", "Malignant Tumor of Gum", "malignant gum neoplasm", "Malignant gum neoplasm", "malignant tumor of gum", "Malignant tumor of gum", "Malignant tumour of gum", "Malignant Gingival Tumor", "malignant gingival tumor", "malignant Gingival tumor", "Malignant Neoplasm of Gum", "malignant neoplasm of gum", "Malignant neoplasm of gum", "Malignant Tumor of the Gum", "malignant gingiva neoplasm", "Malignant tumor of gingiva", "Malignant Tumor of Gingiva", "malignant tumor of gingiva", "malignant tumor of the gum", "Malignant Gingival Neoplasm", "malignant gingival neoplasm", "Malignant tumour of gingiva", "malignant tumour of gingiva", "Malignant Neoplasm of Gingiva", "Malignant Neoplasm of the Gum", "malignant neoplasm of gingiva", "malignant neoplasm of the gum", "malignant tumor of the gingiva", "Malignant Tumor of the Gingiva", "Malignant neoplasm of gum, NOS", "Malignant tumor of gum (disorder)", "malignant neoplasm of the gingiva", "Malignant Neoplasm of the Gingiva", "Malignant tumor of alveolar mucosa", "Malignant tumour of alveolar mucosa", "Malignant neoplasm of gum, unspecified", "malignant neoplasm of other sites of gum", "malignant neoplasm of gingiva (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gingival cancer", "shortest_name_length": 10}
{"curie": "MONDO:0100366", "names": ["occupational disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "occupational disorder", "shortest_name_length": 21}
{"curie": "MONDO:0010589", "names": ["AAS", "FGD", "FGDY", "MRXS16", "Aarskog", "greig syndrome", "Greig syndrome", "Aarskog disease", "greigs syndrome", "Aarskog Disease", "Aarskog syndrome", "MRXS16, included", "Aarskog Syndrome", "aarskog syndrome", "Greig's syndrome", "aarskogs syndrome", "aarskog's syndrome", "Aarskog's syndrome", "Aarskog-like syndrome", "Faciogenital dysplasia", "Scott Aarskog syndrome", "Aarskog Scott syndrome", "Faciogenital Dysplasia", "aarskog-scott syndrome", "shawl scrotum syndrome", "FACIOGENITAL DYSPLASIA", "Aarskog-Scott syndrome", "AARSKOG-SCOTT SYNDROME", "faciogenital dysplasia", "Aarskog-Scott Syndrome", "Scott Aarskog Syndrome", "facio-genital dysplasia", "X-linked Aarskog syndrome", "AARSKOG SYNDROME, X-LINKED", "Aarskog syndrome, X-linked", "Faciodigitogenital Syndrome", "Faciodigitogenital syndrome", "FACIODIGITOGENITAL SYNDROME", "faciodigitogenital syndrome", "Aarskog syndrome (disorder)", "Aarskog-Scott syndrome (ASS)", "facio-digito-genital syndrome", "facio-digito-genital dysplasia", "Facio-Digito-Genital Dysplasia", "facial-digital-genital syndrome", "Aarskog-Scott syndrome, X-linked", "Aarskog-Scott syndrome (diagnosis)", "faciodigitogenital syndrome, recessive", "mental retardation, X-linked, syndromic 16", "Aarskog-Scott syndrome, X-linked recessive", "MENTAL RETARDATION, X-LINKED, SYNDROMIC 16", "mental retardation, X-linked, syndromic 16, included", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 16", "mental retardation, X-linked syndromic 16, X-linked recessive", "FACIOGENITAL DYSPLASIA WITH ATTENTION DEFICIT-HYPERACTIVITY DISORDER", "faciogenital dysplasia with attention Deficit-hyperactivity disorder", "Faciogenital Dysplasia with Attention Deficit-Hyperactivity Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aarskog-Scott syndrome, X-linked", "shortest_name_length": 3}
{"curie": "UMLS:C4682581", "names": ["Stage IC Uterine Corpus Adenosarcoma", "Stage IC Uterine Corpus Adenosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IC Uterine Corpus Adenosarcoma AJCC v8", "shortest_name_length": 36}
{"curie": "MONDO:0008010", "names": ["MSK1", "Msk1", "antigen defined by monoclonal antibody Aj9", "ANTIGEN DEFINED BY MONOCLONAL ANTIBODY AJ9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "antigen defined by monoclonal antibody Aj9", "shortest_name_length": 4}
{"curie": "UMLS:C0855105", "names": ["Burkitt's tumor refractory", "Burkitt's tumour refractory", "Refractory Burkitt Lymphoma", "Burkitt's Lymphoma Refractory", "Refractory Burkitt's Lymphoma", "Burkitt's lymphoma refractory", "Burkitt's tumor or lymphoma refractory", "Burkitt's tumour or lymphoma refractory"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Burkitt's lymphoma refractory", "shortest_name_length": 26}
{"curie": "UMLS:C4682631", "names": ["Stage IIIA1 Fallopian Tube Cancer", "Stage IIIA1 Fallopian Tube Cancer AJCC v8", "Stage IIIA1 Fallopian Tube Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA1 Fallopian Tube Cancer AJCC v8", "shortest_name_length": 33}
{"curie": "MONDO:0019241", "names": ["gamma-glutamyl cycle; disorder", "disorder; gamma-glutamyl cycle", "disorder of gamma-glutamyl cycle", "Disorder of gamma-glutamyl cycle", "Disorders of gamma-glutamyl cycle", "Disorder of the gamma-glutamyl cycle", "disorder of the gamma-glutamyl cycle", "gamma-glutamyl cycle; metabolic disorder", "metabolic disorder; gamma-glutamyl cycle", "Disorder of the gamma-glutamyl cycle, NOS", "inborn disorder of the gamma-glutamyl cycle", "Disorder of the gamma-glutamyl cycle (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of the gamma-glutamyl cycle", "shortest_name_length": 30}
{"curie": "MONDO:0009053", "names": ["ARCL3A", "P5CS deficiency", "De Barsy syndrome A", "DE BARSY SYNDROME A", "De Barsy syndrome a", "cutis laxa type IIIA", "progeroid syndrome of De Barsy", "PROGEROID SYNDROME OF DE BARSY", "cutis laxa type IIIA (diagnosis)", "ALDH18A1-related de Barsy syndrome", "ALDH18A1-related De Barsy syndrome", "Neurocutaneous syndrome, Bicknell type", "neurocutaneous syndrome, Bicknell type", "autosomal recessive cutis laxa type IIIA", "cutis laxa, autosomal recessive, type 3A", "CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA", "cutis laxa, autosomal recessive, type IIIA", "CUTIS LAXA, CORNEAL CLOUDING, AND MENTAL RETARDATION", "cutis laxa, corneal clouding, and mental retardation", "Delta-1-pyrroline 5-carboxylate synthetase deficiency", "cutis laxa, corneal clouding, and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ALDH18A1-related de Barsy syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0021538", "names": ["Ackerman Tumor", "Snuff dipper's cancer", "Mouth Verrucous Carcinoma", "mouth verrucous carcinoma", "Oral Cavity Verrucous Cancer", "Verrucous Carcinoma of Mouth", "oral cavity verrucous cancer", "verrucous carcinoma of mouth", "Oral Cavity Verrucous Carcinoma", "oral cavity verrucous carcinoma", "verrucous carcinoma of the mouth", "Verrucous Carcinoma of the Mouth", "verrucous carcinoma, oral cavity", "Verrucous carcinoma of oral cavity", "verrucous carcinoma of oral cavity", "Verrucous Carcinoma of Oral Cavity", "Verrucous carcinoma of the oral cavity", "Verrucous Carcinoma of the Oral Cavity", "verrucous carcinoma of the oral cavity", "Verrucous carcinoma of oral cavity (disorder)", "verrucous carcinoma of oral cavity (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "verrucous carcinoma of oral cavity", "shortest_name_length": 14}
{"curie": "MONDO:0040673", "names": ["Malignant Peritoneal Germ Cell Tumor", "malignant peritoneal germ cell tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant peritoneal germ cell tumor", "shortest_name_length": 36}
{"curie": "MONDO:0030907", "names": ["MRX106", "XLID106", "X-linked mental retardation 106", "MENTAL RETARDATION, X-LINKED 106", "mental retardation, X-linked 106", "X-linked intellectual disability 106", "intellectual disability, X-linked 106", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 106", "non-syndromic X-linked intellectual disability 106", "intellectual developmental disorder, X-linked 106, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 106", "shortest_name_length": 6}
{"curie": "UMLS:C4053957", "names": ["Systemic Lupus Erythematosus Nephritis Class IV G"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Systemic Lupus Erythematosus Nephritis Class IV G", "shortest_name_length": 49}
{"curie": "MONDO:0008494", "names": ["CHC", "Cryohydrocytosis", "cryohydrocytosis", "CRYOHYDROCYTOSIS", "Pseudohyperkalemia Cardiff", "pseudohyperkalemia Cardiff", "PSEUDOHYPERKALEMIA CARDIFF", "stomatocytosis, cold-sensitive", "STOMATOCYTOSIS, COLD-SENSITIVE", "Stomatocytosis, cold-sensitive", "hereditary cryohydrocytosis with normal stomatin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cryohydrocytosis", "shortest_name_length": 3}
{"curie": "UMLS:C1335338", "names": ["Paranasal Sinus Diffuse Large B-Cell Lymphoma", "Accessory Sinus Diffuse Large B-Cell Lymphoma", "large B-cell diffuse lymphoma of accessory sinus", "Diffuse Large B-Cell Lymphoma of Paranasal Sinus", "Diffuse Large B-Cell Lymphoma of Accessory Sinus", "Diffuse Large B-Cell Lymphoma of the Accessory Sinus", "Diffuse Large B-Cell Lymphoma of the Paranasal Sinus", "Primary Paranasal Sinus Diffuse Large B-Cell Lymphoma", "large B-cell diffuse lymphoma of accessory sinus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "large B-cell diffuse lymphoma of accessory sinus", "shortest_name_length": 45}
{"curie": "MONDO:0020370", "names": ["Iris nevus syndrome", "cogan reese syndrome", "Iris naevus syndrome", "Cogan-Reese Syndrome", "Cogan-Reese syndrome", "cogan-reese syndrome", "cogans reese syndrome", "Nodular unilateral glaucoma", "Cogan-Reese syndrome (disorder)", "Cogan-Reese syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cogan-Reese syndrome", "shortest_name_length": 19}
{"curie": "UMLS:C3828492", "names": ["Pregestational Diabetes", "Pre-Gestational Diabetes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pre-Gestational Diabetes", "shortest_name_length": 23}
{"curie": "MONDO:0007712", "names": ["OAVS with Radial Defect", "Oavs with radial defect", "OAVS WITH RADIAL DEFECT", "Moeschler Clarren syndrome", "Moeschler-Clarren syndrome", "microsomia hemifacial radial defects", "Microsomia Hemifacial Radial Defects", "HEMIFACIAL MICROSOMIA WITH RADIAL DEFECTS", "Hemifacial Microsomia with Radial Defects", "hemifacial microsomia with radial defects", "Hemifacial microsomia-radial defects syndrome", "hemifacial microsomia-radial defects syndrome", "Goldenhar syndrome with ipsilateral radial defect", "Hemifacial microsomia with radial defect syndrome", "GOLDENHAR SYNDROME WITH IPSILATERAL RADIAL DEFECT", "Goldenhar Syndrome with Ipsilateral Radial Defect", "Oculoauriculovertebral Spectrum with Radial Defect", "oculoauriculovertebral spectrum with radial defect", "OCULOAURICULOVERTEBRAL SPECTRUM WITH RADIAL DEFECT", "oculoauriculovertebral spectrum with radial defects", "Oculoauriculovertebral spectrum with radial defects", "Hemifacial microsomia with radial defect syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculoauriculovertebral spectrum with radial defects", "shortest_name_length": 23}
{"curie": "MONDO:0018967", "names": ["short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia", "shortest_name_length": 91}
{"curie": "MONDO:0009881", "names": ["Familial enlargement of the sella turcica", "pituitary dwarfism with large sella turcica", "Pituitary Dwarfism with Large Sella Turcica", "Pituitary dwarfism with large sella turcica", "PITUITARY DWARFISM WITH LARGE SELLA TURCICA", "Pituitary dwarfism with large sella turcica (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pituitary dwarfism with large sella turcica", "shortest_name_length": 41}
{"curie": "MONDO:0011755", "names": ["SLSN3", "senior-loken syndrome 3", "Senior-Loken Syndrome 3", "SENIOR-Loken syndrome 3", "SENIOR-LOKEN SYNDROME 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "senior-loken syndrome 3", "shortest_name_length": 5}
{"curie": "MONDO:0016513", "names": ["alpha-thalassemia-related diseases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alpha-thalassemia-related diseases", "shortest_name_length": 34}
{"curie": "UMLS:C1704378", "names": ["Heymann nephritis", "Heymann Nephritis", "Nephritis, Heymann"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Heymann Nephritis", "shortest_name_length": 17}
{"curie": "MONDO:0021941", "names": ["acute sleeping sickness", "Acute sleeping sickness", "Rhodesian Trypanosomiasis", "Rhodesian trypanosomiasis", "rhodesian trypanosomiasis", "Rhodesian; trypanosomiasis", "Trypanosomiasis, Rhodesian", "trypanosomiasis; Rhodesian", "Rhodesian sleeping sickness", "rhodesian sleeping sickness", "Rhodesiense trypanosomiasis", "East African; trypanosomiasis", "trypanosomiasis; East African", "trypanosomiasis; African, East", "East African sleeping sickness", "African; trypanosomiasis, East", "Rhodesian African sleeping sickness", "Infection by Trypanosoma rhodesiense", "infection by trypanosoma rhodesiense", "infection by Trypanosoma rhodesiense", "infection; Trypanosoma brucei rhodesiense", "Trypanosoma brucei rhodesiense; infection", "Infection caused by Trypanosoma rhodesiense", "infection caused by trypanosoma rhodesiense", "Rhodesian African sleeping sickness (diagnosis)", "trypanosomiasis; Trypanosoma brucei rhodesiense", "Infection caused by Trypanosoma rhodesiense (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infection by Trypanosoma rhodesiense", "shortest_name_length": 23}
{"curie": "UMLS:C4524739", "names": ["Pathologic Stage IIIB Gastroesophageal Junction Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IIIB Gastroesophageal Junction Adenocarcinoma AJCC v8", "shortest_name_length": 70}
{"curie": "MONDO:0005618", "names": ["anxiety", "Anxiety", "Anxiety NOS", "anxiety state", "anxiety disorder", "Anxiety disorder", "Anxiety Disorder", "Disorder;anxiety", "ANXIETY DISORDER", "Disorder, Anxiety", "Anxiety Disorders", "ANXIETY DISORDERS", "anxiety disorders", "Anxiety disorders", "Disorders, Anxiety", "anxiety disorder nos", "Anxiety disorder, NOS", "Anxiety disorder (disorder)", "Unspecified anxiety disorder", "anxiety disorder (diagnosis)", "Anxiety disorder, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anxiety disorder", "shortest_name_length": 7}
{"curie": "MONDO:0000331", "names": ["aneruptive fever", "Rickettsia helvetica spotted fever", "Rickettsia helvetica aneruptive fever", "Rickettsia helvetica infectious disease", "Rickettsia helvetica disease or disorder", "Rickettsia helvetica caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rickettsia helvetica spotted fever", "shortest_name_length": 16}
{"curie": "MONDO:0100233", "names": ["PASC", "long COVID", "long COVID-19", "chronic COVID-19", "long-haul COVID-19", "long haul COVID-19", "post-COVID syndrome", "sequelae of COVID-19", "post-acute sequelae of COVID-19", "post-acute sequelae of SARS-CoV-2 infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "long COVID-19", "shortest_name_length": 4}
{"curie": "UMLS:C0339052", "names": ["globe rupture", "Ruptured Globe", "Rupture of globe", "rupture of globe", "eyeball - rupture of globe", "Rupture of globe (disorder)", "eyeball - rupture of globe (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rupture of globe", "shortest_name_length": 13}
{"curie": "UMLS:C0153783", "names": ["Stage III Lymphocyte Depleted Hodgkin Lymphoma", "Stage III Hodgkin's Lymphoma Lymphocyte Depleted", "Stage III Lymphocyte Depleted Hodgkin's Lymphoma", "Hodgkin's disease lymphocyte depletion type stage III", "Stage III Hodgkin's Disease Lymphocyte Depletion Type", "Stage III Hodgkin's Lymphoma Lymphocyte Depletion Type", "Stage III Lymphocyte Depleted Classical Hodgkin Lymphoma", "Stage III Lymphocyte-Depleted Classical Hodgkin Lymphoma", "Ann Arbor Stage III Lymphocyte-Depleted Classic Hodgkin Lymphoma", "Ann Arbor Stage III Lymphocyte-Depleted Classical Hodgkin Lymphoma", "Lymphocyte depleted Hodgkin lymphoma, lymph nodes of multiple sites", "lymphocyte depleted Hodgkin lymphoma of lymph nodes of multiple sites", "Hodgkin disease, lymphocytic depletion of lymph nodes of multiple sites", "Hodgkin's disease, lymphocytic depletion, lymph nodes of multiple sites", "Hodgkin's disease, lymphocytic depletion of lymph nodes of multiple sites", "lymphocyte depleted Hodgkin lymphoma of lymph nodes of multiple sites (diagnosis)", "Hodgkin's disease, lymphocytic depletion, involving lymph nodes of multiple sites", "Hodgkin's disease, lymphocytic depletion of lymph nodes of multiple sites (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's disease, lymphocytic depletion of lymph nodes of multiple sites", "shortest_name_length": 46}
{"curie": "MONDO:0005212", "names": ["Rhabdosarcoma", "rhabdosarcoma", "RHABDOMYOSARCOMA", "Rhabdomyosarcoma", "rhabdomyosarcoma", "rhabdomyoblastoma", "Rhabdomyosarcomas", "rhabdomyosarcomas", "Rhabdomyosarcoma NOS", "Rhabdomyosarcoma, NOS", "[M]Rhabdomyosarcoma NOS", "rhabdomyosarcoma (disease)", "RHABDOMYOSARCOMA, MALIGNANT", "rhabdomyosarcoma, malignant", "Rhabdomyosarcoma (disorder)", "rhabdomyosarcoma (diagnosis)", "Rhabdomyosarcoma (morphologic abnormality)", "malignant neoplasm myosarcoma rhabdomyosarcoma", "Malignant soft tissue tumor of skeletal muscle differentiation", "Malignant soft tissue tumour of skeletal muscle differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rhabdomyosarcoma", "shortest_name_length": 13}
{"curie": "UMLS:C3839061", "names": ["Malignant Phosphaturic Mesenchymal Tumor", "Phosphaturic mesenchymal tumor, malignant", "Phosphaturic mesenchymal tumour, malignant", "Phosphaturic mesenchymal tumor, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Phosphaturic mesenchymal tumor, malignant", "shortest_name_length": 40}
{"curie": "UMLS:C4763571", "names": ["Colorectal Carcinoma Metastatic in the Liver"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Carcinoma Metastatic in the Liver", "shortest_name_length": 44}
{"curie": "MONDO:0001257", "names": ["Microaneurysm", "microaneurysm", "Microaneurysms", "microaneurysms", "MA-microaneurysm", "microaneurysm retina", "RETINA MICROANEURYSM", "Retinal Microaneurysm", "microaneurysm; retina", "retinal microaneurysm", "Retinal microaneurysm", "Microaneurysm, Retinal", "Retinal Microaneurysms", "Retinal microaneurysms", "retinal microaneurysms", "retinal micro-aneurysms", "Microaneurysms, Retinal", "Charcot-Bouchard Aneurysm", "Retinal microaneurysms NOS", "Retinal microaneurysm, NOS", "RETINAL MICROVASCULAR ANEURYSM", "Retinal microvascular aneurysm", "Microaneurysm of retinal artery", "retinal disorder micro-aneurysms", "microaneurysms of retinal vessels", "retinal micro-aneurysms (diagnosis)", "Microaneurysm (morphologic abnormality)", "Microaneurysm of retinal artery (disorder)", "microaneurysms of retinal vessels (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal microaneurysm", "shortest_name_length": 13}
{"curie": "UMLS:C4520896", "names": ["Stage II Lentigo Maligna", "Stage II Lentigo Maligna Melanoma", "Stage II Lentigo Maligna Melanoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Lentigo Maligna Melanoma AJCC v6 and v7", "shortest_name_length": 24}
{"curie": "MONDO:0014258", "names": ["ASNSD", "ASNS DEFICIENCY", "Asns deficiency", "Asparagine Synthetase Deficiency", "ASPARAGINE SYNTHETASE DEFICIENCY", "asparagine synthetase deficiency", "Asparagine synthetase deficiency", "Congenital microcephaly-severe encephalopathy-progressive cerebral atrophy syndrome", "Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome", "congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome", "Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome (disorder)", "Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0019067", "names": ["idiopathic steroid-sensitive nephrotic syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic steroid-sensitive nephrotic syndrome", "shortest_name_length": 47}
{"curie": "UMLS:C1699742", "names": ["Intraoperative Cardiac Injury", "Intraoperative cardiac injury", "intraoperative cardiac injury", "intraoperative cardiac injury (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraoperative Cardiac Injury", "shortest_name_length": 29}
{"curie": "UMLS:C1518076", "names": ["Lymphoma/Leukemia by Kiel Classification (Antiquated)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoma/Leukemia by Kiel Classification (Antiquated)", "shortest_name_length": 53}
{"curie": "UMLS:C1963763", "names": ["FBSS", "Failed back surgery syndrome", "Failed Back Surgery Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Failed Back Surgery Syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C2064411", "names": ["Liver Kaposi Sarcoma", "Hepatic Kaposi Sarcoma", "hepatic Kaposi's sarcoma", "Kaposi's sarcoma of liver", "Kaposi's sarcoma of liver (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kaposi's sarcoma of liver", "shortest_name_length": 20}
{"curie": "MONDO:0020482", "names": ["myotonia permanens"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myotonia permanens", "shortest_name_length": 18}
{"curie": "UMLS:C1541448", "names": ["recurrent grade I lymphomatoid granulomatosis", "Recurrent Grade I Lymphomatoid Granulomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Grade I Lymphomatoid Granulomatosis", "shortest_name_length": 45}
{"curie": "MESH:D007942", "names": ["Leukemia, Experimental"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leukemia, Experimental", "shortest_name_length": 22}
{"curie": "UMLS:C4054084", "names": ["Refractory Malignant Germ Cell Tumor", "Refractory Childhood Malignant Germ Cell Tumor", "Refractory Childhood Malignant Germ Cell Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Childhood Malignant Germ Cell Tumor", "shortest_name_length": 36}
{"curie": "MONDO:0021005", "names": ["Aarskog syndrome", "faciogenital dysplasia", "Aarskog-Scott syndrome", "faciodigitogenital syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "faciodigitogenital syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0021227", "names": ["ADRENALGLAND", "adrenal tumor", "Adrenal Tumor", "Adrenal Neoplasm", "adrenal neoplasm", "adrenal neoplasms", "Adrenal Neoplasms", "adrenal gland tumor", "Adrenal Gland Tumor", "Tumor of Adrenal Gland", "adrenal gland neoplasm", "Adrenal Gland Neoplasm", "tumor of adrenal gland", "Neoplasm of Adrenal Gland", "neoplasm of adrenal gland", "tumor of the adrenal gland", "Tumor of the Adrenal Gland", "adrenal/paraganglial tumor", "neoplasm of the adrenal gland", "Neoplasm of the Adrenal Gland", "adrenal gland neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adrenal gland neoplasm", "shortest_name_length": 12}
{"curie": "UMLS:C4054363", "names": ["Nephrotic Syndrome - TRPC6 Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - TRPC6 Associated", "shortest_name_length": 37}
{"curie": "MONDO:0015145", "names": ["neurovascular malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurovascular malformation", "shortest_name_length": 26}
{"curie": "MONDO:0016410", "names": ["TSH Deficiency", "TSH deficiency", "central hypothyroid", "HYPOTHYROID CENTRAL", "hypothyroid central", "Central Hypothyroidism", "Thyrotropin Deficiency", "hypothyroidism central", "Central hypothyroidism", "thyrotropin deficiency", "central hypothyroidism", "Central Hypothyroidisms", "Hypothyroidism, central", "Hypothyroidism, Central", "secondary hypothyroidism", "Secondary Hypothyroidism", "Secondary Hypothyroidisms", "Hypothyroidism, Secondary", "Central hypothyroidism, NOS", "Central hypothyroidism (disorder)", "central congenital hypothyroidism", "central hypothyroidism (diagnosis)", "Hypothalamic-Pituitary Hypothyroidism", "hypothalamic-pituitary hypothyroidism", "thyroid stimulating hormone deficiency", "Thyroid Stimulating Hormone Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central congenital hypothyroidism", "shortest_name_length": 14}
{"curie": "UMLS:C4521638", "names": ["Stage I Esophageal Adenocarcinoma", "Clinical Stage I Esophageal Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage I Esophageal Adenocarcinoma AJCC v8", "shortest_name_length": 33}
{"curie": "UMLS:C1142072", "names": ["oral toxicity", "Oral toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral toxicity", "shortest_name_length": 13}
{"curie": "UMLS:C0014856", "names": ["Esophageal fistula", "fistula; esophagus", "Esophageal Fistula", "esophagus; fistula", "esophageal fistula", "Esophageal Fistulas", "Fistula, Esophageal", "oesophageal fistula", "Oesophageal fistula", "esophageal fistulas", "Fistulas, Esophageal", "Esophageal fistula (disorder)", "Esophageal fistula (diagnosis)", "esophageal fistula (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Fistula", "shortest_name_length": 18}
{"curie": "MONDO:0012741", "names": ["HPC12", "Hpc12", "EHBP1 familial prostate cancer", "Prostate Cancer, Hereditary, 12", "prostate cancer, hereditary, 12", "PROSTATE CANCER, HEREDITARY, 12", "prostate cancer, hereditary, type 12", "familial prostate cancer caused by mutation in EHBP1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate cancer, hereditary, 12", "shortest_name_length": 5}
{"curie": "MONDO:0014499", "names": ["MRT46", "mental retardation, autosomal recessive 46", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 46", "mental retardation, autosomal recessive type 46", "intellectual disability, autosomal recessive 46", "intellectual disability, autosomal recessive type 46", "autosomal recessive intellectual developmental disorder 46", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 46", "NDST1 autosomal recessive non-syndromic intellectual disability", "autosomal recessive non-syndromic intellectual disability caused by mutation in NDST1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 46", "shortest_name_length": 5}
{"curie": "UMLS:C0149904", "names": ["Hepatitis cholestatic", "HEPATITIS CHOLESTATIC", "cholestatic hepatitis", "Cholestatic hepatitis", "cholestatic; hepatitis", "hepatitis; cholestatic", "HEPATITIS, CHOLESTATIC", "Cholestatic hepatitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cholestatic hepatitis", "shortest_name_length": 21}
{"curie": "MONDO:0020715", "names": ["MSA1", "MSA1, SUSCEPTIBILITY TO", "MSA1, susceptibility to", "multiple system atrophy, susceptibility to", "multiple system atrophy 1, susceptibility to", "MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple system atrophy 1, susceptibility to", "shortest_name_length": 4}
{"curie": "MONDO:0017263", "names": ["syndromic inherited ichthyosis", "inherited ichthyosis syndromic form", "syndrome associated with inherited ichthyosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited ichthyosis syndromic form", "shortest_name_length": 30}
{"curie": "MONDO:0008640", "names": ["lymphocytic vasculitis", "vasculitis lymphocytic, nodular", "vasculitis, lymphocytic, nodular", "Vasculitis, Lymphocytic, Nodular", "VASCULITIS, LYMPHOCYTIC, NODULAR"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vasculitis, lymphocytic, nodular", "shortest_name_length": 22}
{"curie": "MONDO:0008263", "names": ["Pkd1", "PKD1", "APKD1", "PCLD1", "Apkd1", "POLYCYSTIC KIDNEY DISEASE 1", "polycystic kidney disease 1", "polycystic kidney disease, adult", "polycystic kidney disease type 1", "Polycystic kidney disease, type 1", "PKD1 - Polycystic kidney disease 1", "APKD - Adult type polycystic disease", "Adult Polycystic Kidney Disease Type 1", "Potter type 3 polycystic kidney disease", "polycystic kidney disease, adult, type 1", "POLYCYSTIC KIDNEY DISEASE, ADULT, TYPE I", "Polycystic Kidney Disease, Adult, Type I", "polycystic kidney disease, adult, type I", "Potter Type III Polycystic Kidney Disease", "Adult type polycystic kidney disease type 1", "Potter type 3 polycystic kidney disease, formerly", "PKD1 autosomal dominant polycystic kidney disease", "POTTER TYPE III POLYCYSTIC KIDNEY DISEASE, FORMERLY", "Autosomal dominant polycystic kidney disease type 1", "Autosomal Dominant Polycystic Kidney Disease Type I", "Polycystic Kidney, Type 1 Autosomal Dominant Disease", "Adult type polycystic kidney disease type 1 (disorder)", "POLYCYSTIC LIVER DISEASE 1 WITH OR WITHOUT KIDNEY CYSTS", "polycystic kidney disease 1 with or without polycystic liver disease", "POLYCYSTIC KIDNEY DISEASE 1 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE", "autosomal dominant polycystic kidney disease caused by mutation in PKD1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polycystic kidney disease 1", "shortest_name_length": 4}
{"curie": "UMLS:C2931111", "names": ["Myopia, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myopia, susceptibility to", "shortest_name_length": 25}
{"curie": "UMLS:C0521755", "names": ["Unidirectional Nystagmus", "Unidirectional nystagmus", "nystagmus unidirectional", "Nystagmus, Unidirectional", "Unidirectional nystagmus (disorder)", "Unidirectional nystagmus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unidirectional Nystagmus", "shortest_name_length": 24}
{"curie": "MONDO:0007480", "names": ["MOORE-FEDERMAN SYNDROME", "Moore-Federman Syndrome", "Moore-Federman syndrome", "Moore Federman syndrome", "Moore-Federman syndrome (disorder)", "Familial dwarfism and stiff joints", "Familial dwarfism AND stiff joints", "Dwarfism stiff joint ocular abnormalities", "dwarfism with stiff joints and ocular abnormalities", "DWARFISM WITH STIFF JOINTS AND OCULAR ABNORMALITIES", "Dwarfism with Stiff Joints and Ocular Abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dwarfism with stiff joints and ocular abnormalities", "shortest_name_length": 23}
{"curie": "UMLS:C4521807", "names": ["Stage 0 Appendix Cancer", "Stage 0 Appendix Carcinoma AJCC v8", "Stage 0 Appendiceal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Appendix Carcinoma AJCC v8", "shortest_name_length": 23}
{"curie": "MONDO:0015605", "names": ["Monosomy 9pter", "monosomy 9pter", "9p minus syndrome", "Distal Monosomy 9p", "Distal deletion 9p", "distal monosomy 9p", "Distal monosomy 9p", "distal deletion 9p", "9p Partial Monosomy", "9p monosomy syndrome", "9p- syndrome, partial", "telomeric deletion 9p", "Telomeric deletion 9p", "distal monosomy type 9p", "Distal monosomy 9p syndrome", "9p partial monosomy syndrome", "Deletion 9p syndrome, partial", "Chromosome 9, partial monosomy 9p", "Distal monosomy 9p syndrome (disorder)", "Distal monosomy 9p syndrome (diagnosis)", "9p partial monosomy syndrome (diagnosis)", "Partial deletion of short arm of chromosome 9", "anomaly of chromosome pair 9p partial monosomy syndrome", "deletion of part of chromosome 9 short arm distal monosomy 9p syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal monosomy 9p", "shortest_name_length": 14}
{"curie": "UMLS:C4528570", "names": ["Stage 0 Breast Cancer", "Prognostic Stage 0 Breast Cancer AJCC v8", "Prognostic Stage 0 Breast Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prognostic Stage 0 Breast Cancer AJCC v8", "shortest_name_length": 21}
{"curie": "MONDO:0012897", "names": ["Rosenthal", "c hemophilia", "Hemophilia C", "hemophilia C", "HEMOPHILIA C", "hemophilia c", "haemophilia c", "Haemophilia C", "C; hemophilia", "hemophilia; C", "PTA DEFICIENCY", "F11 deficiency", "F11 DEFICIENCY", "PTA deficiency", "deficiency; PTA", "PTA; deficiency", "rosenthal syndrome", "ROSENTHAL SYNDROME", "Rosenthal Syndrome", "Rosenthal syndrome", "Rosenthals Syndrome", "Rosenthal Syndromes", "Rosenthal's disease", "Syndrome, Rosenthal", "Rosenthal's Syndrome", "Factor XI Deficiency", "factor xi deficiency", "Factor XI deficiency", "Factor 11 Deficiency", "factor XI deficiency", "factor 11 deficiency", "FACTOR XI DEFICIENCY", "Syndrome, Rosenthal's", "Rosenthal's Syndromes", "Deficiency, Factor XI", "Deficiency, Factor 11", "Factor 11 Deficiencies", "Factor XI Deficiencies", "Low factor XI activity", "Deficiencies, Factor 11", "Deficiencies, Factor XI", "Hemophilia C (Factor XI)", "Factor Eleven Deficiency", "Haemophilia C (Factor XI)", "Deficiency, Factor Eleven", "Reduced factor XI activity", "Factor Eleven Deficiencies", "Deficiencies, Factor Eleven", "Rosenthal factor deficiency", "Hereditary factor XI deficiency", "hereditary factor XI deficiency", "Hereditary Factor XI Deficiency", "hereditary Factor XI deficiency", "Congenital factor XI deficiency", "congenital factor XI deficiency", "Thromboplastin antecedent deficiency", "hereditary factor XI deficiency disease", "Hereditary Factor XI Deficiency Disease", "Congenital factor XI deficiency disease", "Hereditary factor XI deficiency disease", "factor XI deficiency, autosomal dominant", "factor XI deficiency, autosomal recessive", "PLASMA THROMBOPLASTIN ANTECEDENT DEFICIENCY", "congenital factor XI deficiency (diagnosis)", "plasma thromboplastin antecedent deficiency", "Plasma Thromboplastin Antecedent Deficiency", "Plasma thromboplastin antecedent deficiency", "plasma thromboplastin; antecedent, deficiency", "Plasma thromboplastin antecedent [PTA] deficiency", "Hereditary factor XI deficiency disease (disorder)", "deficiency; plasma thromboplastin antecedent (PTA)", "deficiency; PTA (plasma thromboplastin antecedent)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital factor XI deficiency", "shortest_name_length": 9}
{"curie": "MONDO:0018248", "names": ["Der(8)t(8;12)", "intellectual disability-seizures-macrocephaly-obesity syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability-seizures-macrocephaly-obesity syndrome", "shortest_name_length": 13}
{"curie": "UMLS:C4526590", "names": ["Stage IIIB Thymic Epithelial Neoplasm AJCC v8", "Stage IIIB Thymus Epithelial Neoplasm AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Thymic Epithelial Neoplasm AJCC v8", "shortest_name_length": 45}
{"curie": "UMLS:C4725802", "names": ["Refractory Malignant Bone Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Malignant Bone Neoplasm", "shortest_name_length": 34}
{"curie": "UMLS:C0149801", "names": ["urosepsis", "UROSEPSIS", "Urosepsis", "sepsis; urinary", "urinary; sepsis", "disorder urosepsis", "urosepsis (diagnosis)", "Sepsis due to urinary tract infection", "Sepsis due to urinary tract infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sepsis due to urinary tract infection", "shortest_name_length": 9}
{"curie": "MONDO:0010028", "names": ["SIALURIA", "sialuria", "Sialuria", "Sialurias", "Salla Disease", "Sialuria (disorder)", "Sialuria, French type", "sialuria, French type", "Sialic acid storage disease", "Sialic Acid Storage Disease", "sialic acid storage disease", "free sialic acid storage disease", "free neuraminic acid storage disease", "N-acetylneuraminic acid storage disease", "N-acetylneuraminic acid (NANA) storage disease (NSD)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sialuria", "shortest_name_length": 8}
{"curie": "MONDO:0004265", "names": ["Acute Endometritis", "acute endometritis", "Acute endometritis", "acute; endometritis", "endometritis, acute", "ENDOMETRITIS, ACUTE", "endometritis; acute", "Acute endometritis (disorder)", "acute endometritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute endometritis", "shortest_name_length": 18}
{"curie": "MONDO:0013344", "names": ["MGR13", "KCNK18 migraine disorder", "migraine disorder caused by mutation in KCNK18", "susceptibility to migraine with or without aura 13", "migraine with or without aura, susceptibility to, 13", "MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 13", "migraine, with or without aura, susceptibility to, 13", "migraine, with or without aura, susceptibility to, type 13"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "migraine, with or without aura, susceptibility to, 13", "shortest_name_length": 5}
{"curie": "UMLS:C2981614", "names": ["Stage IIIB Digestive System Neuroendocrine Tumor", "Stage IIIB Gastrointestinal Neuroendocrine Neoplasm", "Stage IIIB Digestive System Neuroendocrine Neoplasm", "Stage IIIB Digestive System Neuroendocrine Tumor AJCC v7", "Stage IIIB Digestive System Neuroendocrine Neoplasm AJCC v7", "Stage IIIB Gastrointestinal Neuroendocrine Neoplasm AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Digestive System Neuroendocrine Tumor AJCC v7", "shortest_name_length": 48}
{"curie": "MONDO:0001781", "names": ["Uterine Corpus Adenomatoid Tumor", "uterine corpus adenomatoid tumor", "body of uterus adenomatoid tumor", "uterine corpus adenomatoid tumour", "uterine corpus localised epithelial Mesothelioma", "uterine corpus localized epithelial Mesothelioma", "uterine corpus localized epithelial mesothelioma", "Uterine Corpus Localized Epithelial Mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine corpus adenomatoid tumor", "shortest_name_length": 32}
{"curie": "MONDO:0002540", "names": ["Oligodendroglioma", "oligodendroglioma", "childhood oligodendroglioma", "Childhood Oligodendroglioma", "Pediatric Oligodendroglioma", "pediatric oligodendroglioma", "pediatric Oligodendroglioma", "Childhood Oligodendrogliomas", "oligodendroglioma, pediatric", "oligodendroglioma, childhood", "Oligodendroglioma, Childhood", "Oligodendrogliomas, Childhood", "oligodendroglioma of childhood", "pediatric CNS tumor, oligodendroglioma", "childhood CNS tumor, oligodendroglioma", "CNS tumor, pediatric oligodendroglioma", "CNS tumor, childhood oligodendroglioma", "CNS tumor, oligodendroglioma, childhood", "childhood brain tumor, oligodendroglioma", "pediatric brain tumor, oligodendroglioma", "brain tumor, childhood oligodendroglioma", "central nervous system tumor, oligodendroglioma, childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood oligodendroglioma", "shortest_name_length": 17}
{"curie": "MONDO:0004645", "names": ["cheek mucosa cancer", "buccal mucosa cancer", "Cancer of cheek mucosa", "cancer of buccal mucosa", "Cancer of buccal mucosa", "CA - Cancer of cheek mucosa", "CA - Cancer of buccal mucosa", "malignant buccal mucosa tumor", "Malignant Buccal Mucosa Tumor", "Malignant tumor of cheek mucosa", "Malignant Buccal Mucosa Neoplasm", "Malignant Tumor of Buccal Mucosa", "malignant tumor of buccal mucosa", "malignant buccal mucosa neoplasm", "Malignant tumor of buccal mucosa", "Malignant tumour of cheek mucosa", "Malignant tumour of buccal mucosa", "Malignant tumor of internal cheek", "Malignant neoplasm of cheek mucosa", "Malignant tumour of internal cheek", "Malignant Neoplasm of Buccal Mucosa", "Malignant neoplasm of buccal mucosa", "malignant neoplasm of buccal mucosa", "malignant tumor of the buccal mucosa", "Malignant Tumor of the Buccal Mucosa", "Malignant neoplasm of buccal mucosa NOS", "malignant neoplasm of the Buccal Mucosa", "Malignant Neoplasm of the Buccal Mucosa", "malignant neoplasm of the buccal mucosa", "malignant neoplasm of cheek, inner aspect", "Malignant neoplasm of cheek, inner aspect", "Malignant tumor of buccal mucosa (disorder)", "malignant neoplasm of buccal mucosa (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cheek mucosa cancer", "shortest_name_length": 19}
{"curie": "UMLS:C1336449", "names": ["Stage I Ampullary Carcinoma", "Stage I Ampulla of Vater Cancer", "Ampulla of Vater Cancer Stage I", "Stage I Ampulla of Vater Carcinoma", "Stage I Ampulla of Vater Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Ampulla of Vater Cancer AJCC v7", "shortest_name_length": 27}
{"curie": "MONDO:0019681", "names": ["juvenile sialidosis type 2", "dysmorphic sialidosis, juvenile form", "Dysmorphic sialidosis, juvenile form", "Dysmorphic sialidosis, juvenile form (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile sialidosis type 2", "shortest_name_length": 26}
{"curie": "MONDO:0022893", "names": ["craniosynostosis arthrogryposis cleft palate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniosynostosis arthrogryposis cleft palate", "shortest_name_length": 44}
{"curie": "MONDO:0007099", "names": ["amyloidosis 8", "Amyloidosis 8", "AMYLOIDOSIS VIII", "amyloidosis VIII", "Amyloidosis VIII", "amyloidosis, renal", "GERMAN TYPE AMYLOIDOSIS", "German type amyloidosis", "Ostertag type amyloidosis", "OSTERTAG TYPE AMYLOIDOSIS", "Familial renal amyloidosis", "Amyloidosis, Ostertag type", "amyloidosis familial renal", "amyloidosis, Ostertag type", "familial renal amyloidosis", "AMYLOIDOSIS, FAMILIAL RENAL", "amyloidosis, familial renal", "Amyloidosis, familial renal", "familial amyloid nephropathy", "amyloidosis, 3 or more types", "Hereditary renal amyloidosis", "hereditary renal amyloidosis", "Familial amyloid nephropathy", "amyloidosis familial visceral", "familial visceral amyloidosis", "AMYLOIDOSIS, FAMILIAL VISCERAL", "Amyloidosis, familial visceral", "Hereditary amyloid nephropathy", "amyloidosis, familial visceral", "hereditary amyloid nephropathy", "Amyloid nephropathy of Ostertag", "amyloidosis systemic nonneuropathic", "systemic nonneuropathic amyloidosis", "AMYLOIDOSIS, SYSTEMIC NONNEUROPATHIC", "amyloidosis, systemic Nonneuropathic", "Amyloidosis, systemic nonneuropathic", "Familial visceral amyloidosis, Ostertag type", "hereditary amyloidosis with primary renal involement", "Hereditary amyloidosis with primary renal involvement", "Familial visceral amyloidosis, Ostertag type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial visceral amyloidosis", "shortest_name_length": 13}
{"curie": "UMLS:C3897649", "names": ["secondary central nervous system Hodgkin lymphoma", "Secondary Central Nervous System Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary Central Nervous System Hodgkin Lymphoma", "shortest_name_length": 49}
{"curie": "UMLS:C1510888", "names": ["S-T Syndrome", "Angiosarcoma of the Skin of the Arm after Radical Mastectomy followed by Lymphedema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Angiosarcoma of the Skin of the Arm after Radical Mastectomy followed by Lymphedema", "shortest_name_length": 12}
{"curie": "UMLS:C2007076", "names": ["Liver Carcinosarcoma", "Hepatic Carcinosarcoma", "hepatic carcinosarcoma", "carcinosarcoma of liver", "carcinosarcoma of liver (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinosarcoma of liver", "shortest_name_length": 20}
{"curie": "MONDO:0006742", "names": ["Iodine goiter", "simple goitre", "Simple goitre", "simple goiter", "Simple goiter", "Simple Goiter", "iodine goiter", "Endemic goitre", "endemic goitre", "Endemic goiter", "simple; goiter", "goiters iodine", "GOITER ENDEMIC", "Endemic Goiter", "endemic goiter", "struma; simple", "struma; endemic", "Goiter, Endemic", "Goiter, endemic", "Endemic Goiters", "endemic; goiter", "Euthyroid goitre", "Goiters, Endemic", "Euthyroid goiter", "Endemic goiter NOS", "Simple goiter (disorder)", "simple goiter (diagnosis)", "Endemic goiter (disorder)", "Goiter, specified as simple", "Goitre, specified as simple", "iodine deficient endemic goiter", "Simple iodine deficiency goiter", "Simple iodine deficiency goitre", "struma; iodine-deficiency (endemic)", "iodine-deficiency; goiter (endemic)", "Iodine-deficiency-related endemic goiter", "Iodine-deficiency-related endemic goitre", "iodine-deficiency-related endemic goitre", "iodine deficient endemic goiter (diagnosis)", "Iodine-deficiency-related diffuse (endemic) goiter", "Iodine-deficiency-related diffuse (endemic) goitre", "Iodine-deficiency related (endemic) goiter, unspecified", "Iodine-deficiency-related (endemic) goiter, unspecified", "Iodine-deficiency-related (endemic) goitre, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endemic goiter", "shortest_name_length": 13}
{"curie": "UMLS:C0520804", "names": ["Deliberate overdose", "Intentional overdose", "INTENTIONAL OVERDOSE", "Overdose intentional", "OVERDOSE INTENTIONAL", "Non-accidental overdose", "Intentional drug overdose", "Intentional overdose (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intentional overdose", "shortest_name_length": 19}
{"curie": "UMLS:C1512396", "names": ["Blood Borne Cancer", "Hematopoietic and Lymphoid Neoplasm (Antiquated)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hematopoietic and Lymphoid Neoplasm (Antiquated)", "shortest_name_length": 18}
{"curie": "MONDO:0010689", "names": ["CMT4X", "NADMR", "COWCK", "NAMSD", "CMTX4", "CMTX 4", "COWCHOCK SYNDROME", "cowchock syndrome", "Cowchock syndrome", "Cowchock-Fischbeck syndrome", "Cowchock syndrome, X-linked recessive", "X-linked Charcot-Marie-Tooth disease type 4", "Charcot-Marie-Tooth disease X-linked recessive 4", "Charcot-Marie-Tooth disease, X-linked recessive, 4", "Charcot-Marie-Tooth disease X-linked recessive type 4", "X-linked Charcot-Marie-Tooth disease type 4 (disorder)", "CHARCOT-MARIE-TOOTH DISEASE WITH DEAFNESS AND MENTAL RETARDATION", "Charcot-Marie-Tooth disease with deafness and mental retardation", "axonal motor sensory neuropathy with deafness and mental retardation", "Charcot-Marie-Tooth disease with deafness and intellectual disability", "neuropathy, axonal motor-sensory with deafness and mental retardation", "Neuropathy, Axonal Motor-Sensory, with Deafness and Mental Retardation", "neuropathy, axonal motor-sensory, with deafness and mental retardation", "NEUROPATHY, AXONAL MOTOR-SENSORY, WITH DEAFNESS AND MENTAL RETARDATION", "axonal motor sensory neuropathy with deafness and intellectual disability", "neuropathy, axonal motor-sensory with deafness and intellectual disability", "hereditary motor sensory neuropathy II-deafness-mental retardation syndrome", "neuropathy, axonal motor-sensory, with deafness and intellectual disability", "Charcot-Marie syndrome, X-linked, Type II, with deafness and mental retardation", "motor-sensory neuropathy, X-linked Type II, with deafness and mental retardation", "hereditary motor sensory neuropathy (MSN) II-deafness-mental retardation syndrome", "Charcot-Marie-Tooth disease, X-linked Type II, with deafness and mental retardation", "Charcot-Marie-Tooth syndrome, X-linked Type II, with deafness and mental retardation", "CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 4, WITH OR WITHOUT CEREBELLAR ATAXIA", "Charcot-Marie-Tooth (CMT) disease, X-linked Type II, with deafness and mental retardation", "Charcot-Marie-Tooth syndrome (CMTS), X-linked Type II, with deafness and mental retardation", "Charcot-Marie-Tooth-Hoffmann syndrome, X-linked Type II, with deafness and mental retardation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease X-linked recessive 4", "shortest_name_length": 5}
{"curie": "UMLS:C0242006", "names": ["Secondary Myelofibrosis", "secondary myelofibrosis", "Secondary myelofibrosis", "MYELOFIBROSIS, SECONDARY", "Secondary myelofibrosis NOS", "secondary myelofibrosis (diagnosis)", "Myelofibrosis due to another disorder", "Myelofibrosis due to another disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myelofibrosis due to another disorder", "shortest_name_length": 23}
{"curie": "MONDO:0017056", "names": ["Del(21)(q22.13q22.2)", "monosomy 21q22.13q22.2", "monosomy 21q22.13-q22.2", "21q22.13q22.2 microdeletion syndrome", "21q22.13-q22.2 microdeletion syndrome", "DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion", "shortest_name_length": 20}
{"curie": "MONDO:0015056", "names": ["acquired angioedema type 1", "acquired angioneurotic edema type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired angioedema type 1", "shortest_name_length": 26}
{"curie": "MONDO:0001527", "names": ["conjugate gaze palsy", "Conjugate gaze palsy", "conjugate; gaze, palsy", "palsy of conjugate gaze", "Palsy of conjugate gaze", "conjugate gaze palsy (diagnosis)", "Palsy of conjugate gaze (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "conjugate gaze palsy", "shortest_name_length": 20}
{"curie": "UMLS:C0872410", "names": ["posturing", "Posturing"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Posturing", "shortest_name_length": 9}
{"curie": "UMLS:C1336950", "names": ["Vascular Leiomyosarcoma", "Leiomyosarcoma of Vessels", "Leiomyosarcoma of the Vessels"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leiomyosarcoma of Vessels", "shortest_name_length": 23}
{"curie": "MONDO:0013420", "names": ["ARMD12", "age related macular degeneration 12", "macular degeneration, age-related, 12", "MACULAR DEGENERATION, AGE-RELATED, 12", "CX3CR1 age-related macular degeneration", "age related macular degeneration type 12", "macular Degeneration, age-related, type 12", "age-related macular degeneration caused by mutation in CX3CR1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "age related macular degeneration 12", "shortest_name_length": 6}
{"curie": "MONDO:0018448", "names": ["Renal Angiomyoadenomatous Tumor", "Clear Cell Papillary Renal Tumor", "Clear Cell Papillary Renal Neoplasm", "clear cell papillary renal cell carcinoma", "Clear cell papillary renal cell carcinoma", "Clear Cell Papillary Renal Cell Carcinoma", "Clear Cell Tubulopapillary Renal Cell Carcinoma", "Clear cell papillary renal cell carcinoma (disorder)", "Clear cell papillary renal cell carcinoma (diagnosis)", "Clear cell papillary renal cell carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "clear cell papillary renal cell carcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C5420338", "names": ["Salivary Gland Nodular Fasciitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Salivary Gland Nodular Fasciitis", "shortest_name_length": 32}
{"curie": "MONDO:0023650", "names": ["littoral cell angioma", "Littoral cell angioma", "Littoral cell angioma (disorder)", "Littoral cell angioma (diagnosis)", "Littoral cell angioma of the spleen", "littoral cell angioma of the spleen", "Epithelioid hemangioendothelioma of spleen", "Epithelioid haemangioendothelioma of spleen", "neoplasm - soft tissue blood vessel littoral cell angioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "littoral cell angioma of the spleen", "shortest_name_length": 21}
{"curie": "UMLS:C1511272", "names": ["Borderline Uterine Ligament Neoplasm", "Uterine Ligament Neoplasm of Low Malignant Potential"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Uterine Ligament Neoplasm", "shortest_name_length": 36}
{"curie": "MONDO:0006666", "names": ["thyroid atrophy", "Thyroid atrophy", "ATROPHY THYROID", "Thyroid Atrophy", "Atrophy thyroid", "THYROID ATROPHY", "atrophy; thyroid", "thyroid; atrophy", "atrophy of thyroid", "Atrophy of thyroid", "Thyroid atrophy NOS", "thyroid gland atrophy", "Thyroid Gland Atrophy", "Thyroid atrophy (disorder)", "atrophy of thyroid (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrophy of thyroid", "shortest_name_length": 15}
{"curie": "MONDO:0021681", "names": ["VD", "STI", "std", "STD", "vds", "STDs", "STIs", "venereal disease", "VENEREAL DISEASE", "Venereal disease", "disease venereal", "Venereal Disease", "Disease;venereal", "diseases venereal", "venereal; disease", "Venereal Diseases", "venereal diseases", "disease, venereal", "Disease, Venereal", "Diseases, Venereal", "diseases, venereal", "Diseases (Venereal)", "Venereal disease NOS", "VD, venereal disease", "Venereal disease, NOS", "VD - venereal disease", "venereal disease (VD)", "disease (VD), venereal", "disease sexually transmit", "Statutory venereal disease", "sexual; transmitted disease", "disease sexually transmitted", "Sexually Transmitted Disease", "Disease;sexually transmitted", "SEXUALLY TRANSMITTED DISEASE", "Sexually transmitted disease", "sexually transmitted disease", "Sexually Transmitted Disorder", "Sexually transmitted diseases", "disease, sexually Transmitted", "diseases sexually transmitted", "Disease, Sexually Transmitted", "sexually transmitted diseases", "Venereal disease, unspecified", "sexually Transmitted disorder", "Sexually Transmitted Diseases", "Diseases, Sexually Transmitted", "Sexually Transmitted Infection", "sexually Transmitted infection", "Sexually transmissible disease", "diseases, sexually Transmitted", "Sexually transmitted infection", "Sexually transmitted infections", "Transmitted Infection, Sexually", "disease (or disorder); venereal", "Sexually Transmitted Infections", "infection, sexually Transmitted", "Transmitted infection, sexually", "Infection, Sexually Transmitted", "sexually Transmitted infections", "infections, sexually Transmitted", "Infections, Sexually Transmitted", "SEXUALLY TRANSMITTED DISEASE NOS", "Sexually transmitted disease NOS", "Transmitted infections, sexually", "Transmitted Infections, Sexually", "STD - sexually transmitted disease", "STD - Sexually transmitted disease", "sexually transmitted disease (STD)", "STI - sexually transmitted infection", "sexually transmitted diseases (STDs)", "Sexually transmitted infectious disease", "Unspecified sexually transmitted disease", "sexually transmitted disease (diagnosis)", "infectious; disease, sexually transmitted", "disease (or disorder); sexually transmitted", "Sexually transmitted infectious disease, NOS", "Sexually transmitted infectious disease (disorder)", "disease (or disorder); infectious, sexually transmitted", "Disease with a predominantly sexual mode of transmission", "Infections with a predominantly sexual mode of transmission", "Infections with a predominantly sexual mode of transmission (A50-A64)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sexually transmitted disease", "shortest_name_length": 2}
{"curie": "MONDO:0800080", "names": ["severe spondylodysplastic dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe spondylodysplastic dysplasia", "shortest_name_length": 35}
{"curie": "MONDO:0008612", "names": ["TSC1", "tuberose sclerosis", "tuberous sclerosis-1", "Tuberous Sclerosis 1", "tuberous sclerosis 1", "TUBEROUS SCLEROSIS 1", "TSC1 tuberous sclerosis", "tuberous sclerosis type 1", "tuberous sclerosis Complex", "tuberous sclerosis, type 1", "tuberous sclerosis caused by mutation in TSC1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tuberous sclerosis 1", "shortest_name_length": 4}
{"curie": "UMLS:C4525132", "names": ["Stage 0 Rectal Cancer", "Stage 0 Rectal Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Rectal Cancer AJCC v8", "shortest_name_length": 21}
{"curie": "MONDO:0007144", "names": ["Aortic Arch Interruption, Facial Palsy, and Retinal Coloboma", "AORTIC ARCH INTERRUPTION, FACIAL PALSY, AND RETINAL COLOBOMA", "aortic arch interruption, facial palsy, and retinal coloboma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic arch interruption, facial palsy, and retinal coloboma", "shortest_name_length": 60}
{"curie": "MONDO:0012604", "names": ["MCOP3", "MCOPS16", "MCOP3, FORMERLY", "isolated microphthalmia 3", "microphthalmia, isolated 3", "Microphthalmia, Isolated 3", "rax isolated microphthalmia", "RAX isolated microphthalmia", "MICROPHTHALMIA, SYNDROMIC 16", "isolated microphthalmia type 3", "microphthalmia, isolated type 3", "MICROPHTHALMIA, ISOLATED 3, FORMERLY", "isolated microphthalmia caused by mutation in RAX", "isolated microphthalmia caused by mutation in rax"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated microphthalmia 3", "shortest_name_length": 5}
{"curie": "MONDO:0019373", "names": ["DSRCT", "Desmoplastic Small Cell Tumor", "Desmoplastic Small-Cell Tumor", "Tumor, Desmoplastic Small-Cell", "Desmoplastic Small-Cell Tumors", "Small-Cell Tumor, Desmoplastic", "Small-Cell Tumors, Desmoplastic", "Tumors, Desmoplastic Small-Cell", "Desmoplas. small round cell tumor", "desmoplastic small round cell tumor", "desmoplastic small-round-cell tumor", "Desmoplastic small round cell tumor", "Desmoplastic small round-cell tumor", "Desmoplastic Small Round Cell Tumor", "Desmoplastic Small Round-Cell Tumor", "Desmoplastic small round cell tumour", "Polyphenotypic small round cell tumor", "Polyphenotypic Small Round Cell Tumor", "Desmoplastic Small Round-Cell Neoplasm", "Desmoplastic small round-cell neoplasm", "desmoplastic small round-cell neoplasm", "DSRCT - desmoplastic small round cell tumor", "DSRCT - desmoplastic small round cell tumour", "Desmoplastic small round cell tumor (disorder)", "Desmoplastic small round cell tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "desmoplastic small round cell tumor", "shortest_name_length": 5}
{"curie": "UMLS:C5557542", "names": ["Recurrent Appendix Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Appendix Adenocarcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0002238", "names": ["Ca ascending colon", "ascending colon cancer", "ascending cancer colon", "Ascending colon cancer", "COLON ASCENDING CANCER", "cancer of ascending colon", "Malignant neoplasm of right colon", "malignant neoplasm of right colon", "malignant tumor of ascending colon", "Malignant tumor of ascending colon", "malignant ascending colon neoplasm", "Malignant tumour of ascending colon", "Malignant neoplasm of ascending colon", "malignant neoplasm of ascending colon", "Malignant tumor of ascending colon (disorder)", "malignant neoplasm of ascending colon (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ascending colon cancer", "shortest_name_length": 18}
{"curie": "MONDO:0001414", "names": ["spotted bones", "Osteopoikiloses", "Osteopoikilosis", "OSTEOPOIKILOSIS", "osteopoikilosis", "osteopoikilosis (disease)", "Osteopoikilosis (disorder)", "osteopoikilosis (diagnosis)", "osteopathia condensans disseminata"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteopoikilosis", "shortest_name_length": 13}
{"curie": "MONDO:0100019", "names": ["ECHS1-related paroxysmal dyskinesia", "ECHS1 deficiency-associated paroxysmal exercise-induced dyskinesia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ECHS1-related paroxysmal dyskinesia", "shortest_name_length": 35}
{"curie": "MONDO:0015455", "names": ["gonococcal ophthalmia", "Gonococcal ophthalmia", "Ophthalmia Neonatorum", "Gonococcal Conjunctivitis", "Conjunctivitis Gonococcal", "conjunctivitis gonococcal", "GONOCOCCAL CONJUNCTIVITIS", "Gonococcal conjunctivitis", "gonococcal conjunctivitis", "gonococcal ophthalmia neonatorum", "Gonococcal Ophthalmia Neonatorum", "Gonococcal ophthalmia neonatorum", "Gonococcal neonatal conjunctivitis", "Neonatal gonococcal conjunctivitis", "Conjunctivitis gonococcal neonatal", "Gonococcal conjunctivitis (disorder)", "Neonatorum gonococcal conjunctivitis", "gonococcal conjunctivitis neonatorum", "Gonococcal conjunctivitis neonatorum", "gonococcal conjunctivitis (diagnosis)", "Gonococcal conjunctivitis (neonatorum)", "Opthalmia neonatorum caused by Neisseria", "Neisseria gonorrheae neonatal conjunctivitis", "Neisseria gonorrhoeae neonatal conjunctivitis", "neonatorum; ophthalmia, gonococcal (etiology)", "ophthalmia; neonatorum, gonococcal (etiology)", "Gonococcal conjunctivitis neonatorum (disorder)", "gonococcal conjunctivitis neonatorum (diagnosis)", "ophthalmia; neonatorum, gonococcal (manifestation)", "neonatorum; ophthalmia, gonococcal (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gonococcal conjunctivitis", "shortest_name_length": 21}
{"curie": "UMLS:C1167766", "names": ["Wound infection pseudomonas", "Pseudomonas wound infection", "Pseudomonas wound infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wound infection pseudomonas", "shortest_name_length": 27}
{"curie": "UMLS:C4552926", "names": ["IB1", "Stage IB1 Cervical Cancer", "Stage IB1 Cervical Cancer AJCC v8", "Stage IB1 Cervical Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB1 Cervical Cancer AJCC v8", "shortest_name_length": 3}
{"curie": "MONDO:0024341", "names": ["retinal cell tumor", "Retinal Cell Tumor", "Retinal Cell Neoplasm", "retinal cell neoplasm", "retinal neural cell neoplasm", "Retinal Neural Cell Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal cell neoplasm", "shortest_name_length": 18}
{"curie": "MONDO:0060702", "names": ["SEMDDR", "spondyloepimetaphyseal dysplasia, di rocco type", "spondyloepimetaphyseal dysplasia, Di Rocco type", "SPONDYLOEPIMETAPHYSEAL DYSPLASIA, DI ROCCO TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepimetaphyseal dysplasia, di rocco type", "shortest_name_length": 6}
{"curie": "MONDO:0014471", "names": ["COXPD22", "Isolated ATP synthase deficiency", "isolated ATP synthase deficiency", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 22", "mitochondrial complex V (ATP synthase) deficiency", "Isolated adenosine triphosphate synthase deficiency", "Isolated mitochondrial respiratory chain complex V deficiency", "isolated mitochondrial respiratory chain complex V deficiency", "Isolated adenosine triphosphate synthase deficiency (disorder)", "mitochondrial proton-transporting ATP synthase complex deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial proton-transporting ATP synthase complex deficiency", "shortest_name_length": 7}
{"curie": "MONDO:0010679", "names": ["DMD", "Duchenne", "Duchenne syndrome", "Duchenne dystrophy", "Duchenne-Griesinger", "Duchenne myodystrophy", "motor; neuron, Duchenne", "Duchenne type; dystrophy", "dystrophy; Duchenne type", "Duchenne muscular dystrophy", "MUSCULAR DYSTROPHY DUCHENNE", "DUCHENNE MUSCULAR DYSTROPHY", "duchenne muscular dystrophy", "X-linked muscular dystrophy", "Duchenne Muscular Dystrophy", "Cardiomyopathy, Dilated, 3B", "x-linked muscular dystrophy", "Muscular dystrophy, Duchenne", "muscular dystrophy, Duchenne", "Duchenne; muscular dystrophy", "duchenne-griesinger syndrome", "Muscular Dystrophy, Duchenne", "Duchenne-Griesinger syndrome", "muscular dystrophy; Duchenne", "duchenne's muscular dystrophy", "Duchenne's Muscular Dystrophy", "Duchenne; motor neuron disease", "X-linked dilated cardiomyopathy", "DMD - Duchenne muscular dystrophy", "Muscular Dystrophy, Duchenne Type", "muscular dystrophy, Duchenne type", "Duchenne muscular dystrophy (DMD)", "duchenne muscular dystrophy (DMD)", "Cardiomyopathy, Dilated, X-Linked", "MUSCULAR DYSTROPHY, DUCHENNE TYPE", "muscular; dystrophy, Duchenne type", "dystrophy; muscular, Duchenne type", "Benign Duchenne muscular dystrophy", "Pseudohypertrophic muscular dystrophy", "Pseudohypertrophic Muscular Dystrophy", "pseudohypertrophic muscular paralysis", "X-linked recessive muscular dystrophy", "Muscular Dystrophy, Pseudohypertrophic", "Severe dystrophinopathy, Duchenne type", "X-linked dilated cardiomyopathy (XLCM)", "severe dystrophinopathy, Duchenne type", "Duchenne muscular dystrophy (disorder)", "Duchenne muscular dystrophy (diagnosis)", "Duchenne de Boulogne muscular dystrophy", "progressive muscular dystrophy (Duchenne)", "mild X-linked recessive muscular dystrophy", "progressive muscular dystrophy of childhood", "pseudohypertrophic adult muscular dystrophy", "adult pseudohypertrophic muscular dystrophy", "Duchenne-Type Progressive Muscular Dystrophy", "Duchenne Type Progressive Muscular Dystrophy", "benign X-linked recessive muscular dystrophy", "Progressive muscular dystrophy, Duchenne type", "progressive muscular dystrophy, Duchenne type", "Progressive Muscular Dystrophy, Duchenne Type", "classic X-linked recessive muscular dystrophy", "Severe generalized familial muscular dystrophy", "Duchenne pseudohypertrophic muscular dystrophy", "Childhood Pseudohypertrophic Muscular Dystrophy", "childhood pseudohypertrophic muscular dystrophy", "Pseudohypertrophic Childhood Muscular Dystrophy", "Duchenne muscular dystrophy, X-linked recessive", "Childhood Muscular Dystrophy, Pseudohypertrophic", "Pseudohypertrophic Muscular Dystrophy, Childhood", "Muscular Dystrophy, Childhood, Pseudohypertrophic", "MUSCULAR DYSTROPHY, PSEUDOHYPERTROPHIC, CHILDHOOD", "pseudohypertrophic progressive muscular dystrophy", "Muscular Dystrophy, Pseudohypertrophic, Childhood", "pseudohypertrophic progressive muscular dystrophy, Duchenne type", "MUSCULAR DYSTROPHY, PSEUDOHYPERTROPHIC PROGRESSIVE, DUCHENNE TYPE", "muscular dystrophy, pseudohypertrophic progressive, Duchenne type", "Muscular Dystrophy, Pseudohypertrophic Progressive, Duchenne Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Duchenne muscular dystrophy", "shortest_name_length": 3}
{"curie": "MONDO:0030334", "names": ["IIAE11", "ENCEPHALITIS, ACUTE, INFECTION (VIRAL)-INDUCED, SUSCEPTIBILITY TO, 11", "encephalitis, acute, infection (viral)-induced, susceptibility to, 11", "ENCEPHALITIS, ACUTE, INFECTION-INDUCED (VIRAL), SUSCEPTIBILITY TO, 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephalitis, acute, infection (viral)-induced, susceptibility to, 11", "shortest_name_length": 6}
{"curie": "UMLS:C5556678", "names": ["Cervical Adenocarcinoma, NOS", "Invasive Cervical Adenocarcinoma, NOS", "Cervical Adenocarcinoma, Not Otherwise Specified", "Invasive Cervical Adenocarcinoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Adenocarcinoma, Not Otherwise Specified", "shortest_name_length": 28}
{"curie": "UMLS:C4520754", "names": ["stage III oropharynx cancer", "Stage III Oropharyngeal Throat Cancer", "Stage III Oropharynx Carcinoma AJCC v6", "Stage III Oropharyngeal Cancer AJCC v6", "Oropharyngeal Cancer, Stage III AJCC v6", "Stage III Carcinoma of Oropharynx AJCC v6", "Stage III Oropharyngeal Carcinoma AJCC v6", "Stage III Carcinoma of the Oropharynx AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Oropharyngeal Carcinoma AJCC v6", "shortest_name_length": 27}
{"curie": "MONDO:0014543", "names": ["CMS14", "CMSTA3", "congenital myasthenic syndrome 14", "MYASTHENIC SYNDROME, CONGENITAL, 14", "myasthenic syndrome, congenital, 14", "congenital myasthenic syndrome type 14", "myasthenic syndrome, congenital, type 14", "congenital myasthenic syndrome with tubular aggregates 3", "MYASTHENIC SYNDROME, CONGENITAL, WITH TUBULAR AGGREGATES 3", "congenital myasthenic syndrome 14, with tubular aggregates", "myasthenic syndrome, congenital, with tubular aggregates 3", "myasthenic syndrome, congenital, 14, with tubular aggregates", "ALG2 congenital myasthenic syndromes with glycosylation defect", "congenital myasthenic syndromes with glycosylation defect caused by mutation in ALG2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myasthenic syndrome 14", "shortest_name_length": 5}
{"curie": "MONDO:0016765", "names": ["Del(19)(p13.12)", "monosomy 19p13.12", "Monosomy 19p13.12", "19p13.12 microdeletion syndrome", "Chromosome19p13.12 microdeletion", "19p13.12 microdeletion syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "19p13.12 microdeletion syndrome", "shortest_name_length": 15}
{"curie": "UMLS:C0522178", "names": ["THOUGHTS OF SELF HARM", "Thoughts of self harm", "thoughts of self-harm", "Self-injurious ideation", "Thoughts of self harm (finding)", "thoughts of self-harm (symptom)", "clinical finding thoughts of self harm", "Thoughts of self harm (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thoughts of self harm", "shortest_name_length": 21}
{"curie": "UMLS:C1868770", "names": ["Injection site recall reaction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site recall reaction", "shortest_name_length": 30}
{"curie": "UMLS:C4521630", "names": ["Stage I Laryngeal Throat Cancer", "Stage I Laryngeal Cancer AJCC v8", "Stage I Laryngeal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Laryngeal Cancer AJCC v8", "shortest_name_length": 31}
{"curie": "MONDO:0030878", "names": ["KABAMAS", "Kaya-Barakat-Masson syndrome", "KAYA-BARAKAT-MASSON SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kaya-Barakat-Masson syndrome", "shortest_name_length": 7}
{"curie": "UMLS:C0853970", "names": ["Large bowel stricture", "Large intestinal stenosis", "Large intestinal stricture", "Large intestinal stricture NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Large intestinal stenosis", "shortest_name_length": 21}
{"curie": "MONDO:0013760", "names": ["ISQMR", "ELOVL4-related neuro ichthyosis", "ichthyosis, spastic quadriplegia, and mental retardation", "ICHTHYOSIS, SPASTIC QUADRIPLEGIA, AND MENTAL RETARDATION", "ichthyosis, spastic quadriplegia, and intellectual disability", "ICHTHYOSIS, SPASTIC QUADRIPLEGIA, AND IMPAIRED INTELLECTUAL DEVELOPMENT", "Congenital ichthyosis-intellectual disability-spastic tetraplegia syndrome", "congenital ichthyosis-intellectual disability-spastic tetraplegia syndrome", "congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome", "Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome", "Congenital ichthyosis, intellectual disability, spastic quadriplegia syndrome", "ELOVL4 (elongation of very long chain fatty acids-like 4) related neuro ichthyosis", "Congenital ichthyosis, intellectual disability, spastic quadriplegia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0035002", "names": ["isolated inherited retinal disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated inherited retinal disorder", "shortest_name_length": 35}
{"curie": "MONDO:0020809", "names": ["Benign Androblastoma", "benign sertoli cell tumor", "Benign Sertoli Cell Tumor", "SERTOLI CELL TUMOR, BENIGN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign sertoli cell tumor", "shortest_name_length": 20}
{"curie": "MONDO:0017761", "names": ["disorder of mineral absorption and transport"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of mineral absorption and transport", "shortest_name_length": 44}
{"curie": "MONDO:0033004", "names": ["PKD4", "PKD3", "PKD3, formerly", "polycystic kidney disease 4", "hepatic fibrosis, congenital", "polycystic kidney and hepatic disease 1", "polycystic kidney disease, infantile, type 1", "polycystic kidney disease, autosomal recessive", "polycystic kidney disease 4 with or without hepatic disease", "polycystic kidney disease 4, with or without hepatic disease", "polycystic kidney disease 4 with or without polycystic liver disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polycystic kidney disease 4", "shortest_name_length": 4}
{"curie": "MONDO:0006605", "names": ["Scalp Dermatosis", "Scalp Dermatoses", "scalp dermatosis", "Dermatoses, Scalp", "Dermatosis, Scalp", "dermatosis of scalp", "Dermatosis of scalp", "Dermatosis of scalp (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scalp dermatosis", "shortest_name_length": 16}
{"curie": "MONDO:0010721", "names": ["Reticuloendotheliosis", "reticuloendotheliosis", "RETICULOENDOTHELIOSIS", "reticuloendotheliosis, X-linked", "Reticuloendotheliosis, X-linked", "Reticuloendothelial hyperplasia", "Reticuloendothelial Hyperplasia", "RETICULOENDOTHELIOSIS, X-LINKED", "RETICULOENDOTHELIAL HYPERPLASIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "reticuloendotheliosis, X-linked", "shortest_name_length": 21}
{"curie": "UMLS:C0153225", "names": ["Meningitis gonococcal", "gonococcal meningitis", "Gonococcal meningitis", "Meningitis due to gonococcus", "Gonococcal meningitis (disorder)", "gonococcal meningitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gonococcal meningitis", "shortest_name_length": 21}
{"curie": "MONDO:0001003", "names": ["talcosis", "Talcosis", "Talc lung disease", "pulmonary talcosis", "Pulmonary talcosis", "TALCOSIS, PULMONARY", "talc pneumoconiosis", "Talc pneumoconiosis", "Talc Pneumoconiosis", "pneumoconiosis; talc", "talc; pneumoconiosis", "PNEUMOCONIOSIS, TALC", "pneumoconiosis due to talc", "Pneumoconiosis due to talc", "fibrosis; lung, due to talc", "lung; fibrosis, due to talc", "Talc workers' pneumoconiosis", "Pneumoconiosis caused by talc", "Pneumoconiosis due to talc dust", "pneumoconiosis due to talc (diagnosis)", "Pneumoconiosis caused by talc (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pneumoconiosis due to talc", "shortest_name_length": 8}
{"curie": "MONDO:0007142", "names": ["TBS", "TBS1", "REAR syndrome", "rear syndrome", "REAR SYNDROME", "towne syndrome", "Townes Syndrome", "Townes syndrome", "townes syndrome", "rearing syndrome", "syndrome towne brock", "syndrome townes brock", "Townes Brocks syndrome", "anus-hand-ear syndrome", "Townes-Brocks Syndrome", "Townes-Brocks syndrome", "townes-brocks syndrome", "TOWNES-BROCKS SYNDROME", "Townes-Brocks syndrome 1", "Townes syndrome (disorder)", "Townes-Brocks syndrome (TBS)", "renal-Ear-anal-radial syndrome", "renal-ear-anal-radial syndrome", "Renal-ear-anal-radial syndrome", "RENAL-EAR-ANAL-RADIAL SYNDROME", "Renal-Ear-Anal-Radial Syndrome (Rear)", "Anal-Ear-Renal-Radial Malformation Syndrome", "anal-ear-renal-radial malformation syndrome", "Townes-Brocks-branchiootorenal-like syndrome", "Imperforate Anus-Hand and Foot Anomalies Syndrome", "imperforate anus-hand and foot anomalies syndrome", "imperforate anus with hand, foot and ear anomalies", "anus, imperforate, with hand, foot and ear anomalies", "anus, imperforate, with hand, foot, and Ear anomalies", "Anus, Imperforate, with Hand, Foot, and Ear Anomalies", "ANUS, IMPERFORATE, WITH HAND, FOOT, AND EAR ANOMALIES", "deafness-imperforate anus-hypoplastic thumbs syndrome", "Deafness-Imperforate Anus-Hypoplastic Thumbs Syndrome", "Imperforate anus-hand, foot and ear anomalies syndrome", "DEAFNESS, SENSORINEURAL, WITH IMPERFORATE ANUS AND THUMB ANOMALIES", "deafness, sensorineural, with imperforate anus and thumb anomalies", "Deafness, Sensorineural, With Imperforate Anus And Thumb Anomalies", "sensorineural deafness with imperforate anus and hypoplastic thumbs", "Sensorineural deafness with imperforate anus and hypoplastic thumbs", "Sensorineural Deafness-Imperforate Anus-Hypoplastic Thumbs Syndrome", "sensorineural deafness-imperforate anus-hypoplastic thumbs syndrome", "Deafness, sensorineural, with imperforate anus and hypoplastic thumbs", "deafness, sensorineural, with imperforate anus and hypoplastic thumbs", "Sensorineural hearing loss with imperforate anus and hypoplastic thumbs"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Townes-Brocks syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0003455", "names": ["IPN", "Bile Duct IPN", "biliary papillomatosis", "Biliary papillomatosis", "Biliary Papillomatosis", "bile duct papillomatosis", "Bile Duct Papillomatosis", "Glandular Papillomatosis", "Papillomatosis, glandular", "bile duct papillary neoplasm", "intraductal papillary neoplasm", "Biliary papillomatosis (disorder)", "Intraductal papillary neoplasm, NOS", "bile duct papillary epithelial neoplasm", "Bile Duct Intraductal Papillary Neoplasm", "Papillomatosis, glandular (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bile duct papillary neoplasm", "shortest_name_length": 3}
{"curie": "MONDO:0005376", "names": ["mgn", "membranous nephropathy", "Membranous nephropathy", "Membranous Nephropathy", "nephropathy membranous", "Nephropathy, Membranous", "NEPHROPATHY, MEMBRANOUS", "MEMBRANOUS GLOMERULOPATHY", "Membranous Glomerulopathy", "membranous glomerulopathy", "Glomerulopathy, Membranous", "Membranous nephropathy NOS", "GLOMERULOPATHY, MEMBRANOUS", "GLOMERULONEPHRITIS MEMBRANOUS", "Membranous glomerulonephritis", "membranous glomerulonephritis", "Glomerulonephritis membranous", "glomerulonephritis membranous", "Membranous Glomerulonephritis", "Glomerulonephritis, Membranous", "Extramembranous Glomerulopathy", "GLOMERULONEPHRITIS, MEMBRANOUS", "Glomerulopathy, Extramembranous", "membranous Glomerulonephropathy", "membranous glomerulonephropathy", "Membranous glomerulonephropathy", "Membranous Glomerulonephritides", "Membranous Glomerulonephropathy", "Glomerulonephritides, Membranous", "Glomerulonephropathy, Membranous", "Membranous glomerulonephritis NOS", "membranous nephropathy (diagnosis)", "MGN - Membranous glomerulonephritis", "Membranous glomerulonephritis (disorder)", "membranous glomerulonephritis (diagnosis)", "Chronic nephritic syndrome, diffuse membranous glomerulonephritis", "chronic nephritic syndrome with diffuse membranous glomerulonephritis", "Chronic nephritic syndrome with diffuse membranous glomerulonephritis", "chronic nephritic syndrome with diffuse membranous glomerulonephritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "membranous glomerulonephritis", "shortest_name_length": 3}
{"curie": "UMLS:C1333449", "names": ["High-Grade Esophageal Glandular Dysplasia", "High-Grade Esophageal Glandular Intraepithelial Neoplasia", "High Grade Esophageal Glandular Intraepithelial Neoplasia", "Esophageal High-Grade Glandular Intraepithelial Neoplasia", "Esophageal glandular dysplasia (intraepithelial neoplasia), high grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Esophageal Glandular Intraepithelial Neoplasia", "shortest_name_length": 41}
{"curie": "UMLS:C0742136", "names": ["Cervical warts", "Cervical Condyloma", "CERVICAL CONDYLOMA", "Cervix Condylomata", "Condyloma of Cervix", "Cervix Uteri Condyloma", "Condyloma of the Cervix", "Uterine Cervix Condyloma", "UTERINE CERVIX, CONDYLOMA", "Condyloma of Cervix Uteri", "Condyloma of Uterine Cervix", "Cervix Condylomata Acuminata", "Condyloma of the Cervix Uteri", "Cervical Condyloma Acuminatum", "Condyloma acuminata of cervix", "condyloma acuminatum of cervix", "Condylomata Acuminata of Cervix", "Condyloma of the Uterine Cervix", "Uterine Cervix Condyloma Acuminatum", "Condylomata Acuminata of the Cervix", "Condylomata Acuminata of Cervix Uteri", "Condylomata Acuminata of Uterine Cervix", "Condyloma acuminata of cervix (disorder)", "Condylomata Acuminata of the Cervix Uteri", "condyloma acuminatum of cervix (diagnosis)", "Condylomata Acuminata of the Uterine Cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Condyloma acuminata of cervix", "shortest_name_length": 14}
{"curie": "MONDO:0003733", "names": ["mature teratoma", "CNS mature teratoma", "CNS Mature Teratoma", "mature teratoma of CNS", "Mature Teratoma of CNS", "Mature teratoma of the CNS", "mature teratoma of the CNS", "Mature Teratoma of the CNS", "central nervous system mature teratoma", "Central Nervous System Mature Teratoma", "mature teratoma of central nervous system", "Mature Teratoma of Central Nervous System", "mature teratoma of the central nervous system", "Mature Teratoma of the Central Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system mature teratoma", "shortest_name_length": 15}
{"curie": "MONDO:0011837", "names": ["VKCFD2", "combined deficiency of vitamin K-dependent clotting factors 2", "VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 2", "vitamin K-dependent clotting factors, combined deficiency of, 2", "Vitamin K-Dependent Clotting Factors, Combined Deficiency Of, Type 2", "vitamin K-dependent clotting factors, combined deficiency of, type 2", "VKORC1 congenital vitamin K-dependent coagulation factors combined deficiency", "congenital vitamin K-dependent coagulation factors combined deficiency caused by mutation in VKORC1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitamin K-dependent clotting factors, combined deficiency of, type 2", "shortest_name_length": 6}
{"curie": "UMLS:C0278665", "names": ["Recurrent Soft Tissue Sarcoma", "Relapsed Adult Soft Tissue Sarcoma", "Recurrent Adult Soft Tissue Sarcoma", "recurrent adult soft tissue sarcoma", "adult soft tissue sarcoma, recurrent", "soft tissue sarcoma, adult, recurrent", "Relapsed Adult Sarcoma of Soft Tissue", "sarcoma, adult soft tissue, recurrent", "Recurrent Adult Sarcoma of Soft Tissue", "Relapsed Adult Sarcoma of the Soft Tissue", "Recurrent Adult Sarcoma of the Soft Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Adult Soft Tissue Sarcoma", "shortest_name_length": 29}
{"curie": "MONDO:0002461", "names": ["mpgn", "MPGN", "Primary MPGN", "Lobular glomerulonephritis", "lobular glomerulonephritis", "Chronic lobular glomerulonephritis", "Chronic glomerulonephritis, lobular", "chronic glomerulonephritis, lobular", "Mesangiocapillary Glomerulonephritis", "glomerulonephritis mesangiocapillary", "Mesangiocapillary glomerulonephritis", "GLOMERULONEPHRITIS, MESANGIOCAPILLARY", "Hypocomplementemic Glomerulonephritis", "Glomerulonephritis, Mesangiocapillary", "Mesangiocapillary Glomerulonephritides", "Mesangial capillary glomerulonephritis", "Glomerulonephritis, Hypocomplementemic", "Hypocomplementemic Glomerulonephritides", "Membranoproliferative glomerulonephritis", "Membranoproliferative Glomerulonephritis", "membranoproliferative glomerulonephritis", "Glomerulonephritis membranoproliferative", "GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE", "glomerulonephritis membranoproliferative", "Glomerulonephritis, membranoproliferative", "Glomerulonephritis, Membranoproliferative", "Mesangiocapillary glomerulonephritis, NOS", "GLOMERULONEPHRITIS, MEMBRANOPROLIFERATIVE", "Membranoproliferative Glomerulonephritides", "MCGN - Mesangiocapillary glomerulonephritis", "Glomerulonephritides, Membranoproliferative", "Membranoproliferative glomerulonephritis NOS", "MPGN Membranoproliferative Glomerulonephritis", "Membranoproliferative Glomerulonephritis, MPGN", "Glomerulonephritis, MPGN Membranoproliferative", "MPGN - Membranoproliferative glomerulonephritis", "MPGN Membranoproliferative Glomerulonephritides", "membranoproliferative glomerulonephritis (MPGN)", "GLOMERULONEPHRITIS, HYPOCOMPLEMENTEMIC, CHRONIC", "Mesangiocapillary glomerulonephritis (disorder)", "Primary membranoproliferative glomerulonephritis", "Glomerulonephritides, MPGN Membranoproliferative", "Mesangiocapillary glomerulonephritis (diagnosis)", "Membranoproliferative Glomerulonephritides, MPGN", "membranoproliferative glomerulonephritis (disease)", "Membranoproliferative glomerulonephritis (diagnosis)", "nephropathy due to membranoproliferative glomerulonephritis", "nephropathy due to membranoproliferative glomerulonephritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "membranoproliferative glomerulonephritis", "shortest_name_length": 4}
{"curie": "MONDO:0022787", "names": ["cleft palate heart disease polydactyly absent tibia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleft palate heart disease polydactyly absent tibia", "shortest_name_length": 51}
{"curie": "MONDO:0021169", "names": ["Epithelioid hemangioma", "Epithelioid Hemangioma", "epithelioid hemangioma", "hemangioma; epithelioid", "epithelioid haemangioma", "histiocytoid hemangioma", "Histiocytoid hemangioma", "Histiocytoid Hemangioma", "epithelioid; hemangioma", "Epithelioid haemangioma", "Histiocytoid Hemangiomas", "Histiocytoid haemangioma", "hemangioma; histiocytoid", "Hemangioma, Histiocytoid", "histiocytoid; hemangioma", "Hemangiomas, Histiocytoid", "[M] Epithelioid hemangioma", "[M] Epithelioid haemangioma", "[M] Histiocytoid hemangioma", "[M] Histiocytoid haemangioma", "adult epithelioid hemangioma", "Angiolymphoid hyperplasia with eosinophilia", "angiolymphoid hyperplasia with eosinophilia", "Angiolymphoid Hyperplasia with Eosinophilia", "Epithelioid hemangioma (morphologic abnormality)", "Angiolymphoid hyperplasia with eosinophilia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epithelioid hemangioma", "shortest_name_length": 22}
{"curie": "UMLS:C0751799", "names": ["Traumatic Brain Hemorrhage", "Brain Hemorrhage, Traumatic", "Hemorrhage, Traumatic Brain", "Traumatic Brain Hemorrhages", "Brain Hemorrhages, Traumatic", "hemorrhage; brain, traumatic", "brain; hemorrhage, traumatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brain Hemorrhage, Traumatic", "shortest_name_length": 26}
{"curie": "UMLS:C1336195", "names": ["Stage IIB Small Cell Lung Cancer", "Stage IIB Small Cell Lung Carcinoma", "Stage IIB Small Cell Carcinoma of Lung", "Stage IIB Small Cell Carcinoma of the Lung", "Stage IIB Lung Small Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Lung Small Cell Carcinoma AJCC v7", "shortest_name_length": 32}
{"curie": "MONDO:0030702", "names": ["autoimmune atherosclerosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune atherosclerosis", "shortest_name_length": 26}
{"curie": "UMLS:C0475589", "names": ["Germinal Matrix Hemorrhage of Newborn", "Germinal Matrix Hemorrhage of the Newborn", "grade I neonatal intraventricular hemorrhage", "grade I intraventricular hemorrhage neonatal", "Intraventricular Hemorrhage of Newborn Grade 1", "Grade 1 Intraventricular Hemorrhage of the Newborn", "Subependymal Germinal Matrix Hemorrhage of Newborn", "grade I neonatal intraventricular hemorrhage (diagnosis)", "Grade 1 Intraventricular (Nontraumatic) Hemorrhage of Fetus and Newborn", "Intraventricular (nontraumatic) hemorrhage, grade 1, of fetus and newborn", "Intraventricular (Nontraumatic) Hemorrhage, Grade 1, of Fetus and Newborn", "Intraventricular (nontraumatic) haemorrhage, grade 1, of fetus and newborn", "Intraventricular (nontraumatic) haemorrhage, grade 1, of foetus and newborn", "Intraventricular (nontraumatic) hemorrhage, grade 1, of fetus and newborn (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraventricular (nontraumatic) hemorrhage, grade 1, of fetus and newborn", "shortest_name_length": 37}
{"curie": "MONDO:0000686", "names": ["Pure alexia", "pure alexia", "Pure Alexia", "Pure alexias", "Pure Alexias", "Alexia, Pure", "Alexias, Pure", "alexias, Pure", "Pure Word blindness", "pure word blindness", "Pure Word Blindness", "Word blindness, Pure", "Blindness, Pure Word", "Word Blindness, Pure", "blindness, Pure Word", "visual verbal agnosia", "Visual Verbal Agnosia", "Pure Word Blindnesses", "Visual Verbal Agnosias", "Blindnesses, Pure Word", "Word Blindnesses, Pure", "Verbal Agnosia, Visual", "agnosia, visual verbal", "verbal agnosia, visual", "Agnosia, Visual Verbal", "visual verbal Agnosias", "verbal Agnosias, visual", "agnosia; verbal, visual", "Agnosias, visual verbal", "Verbal Agnosias, Visual", "Alexia Without Agraphia", "alexia without agraphia", "Agnosias, Visual Verbal", "verbal; agnosia, visual", "without agraphia, alexia", "Without Agraphia, Alexia", "Agraphia, Alexia Without", "Alexia Without Agraphias", "alexia without Agraphias", "agraphia, alexia without", "Agraphias, alexia without", "Without Agraphias, Alexia", "without Agraphias, alexia", "Agraphias, Alexia Without", "Pure alexia without agraphia", "Pure Alexia Without Agraphia", "alexia syndrome without agraphia", "Alexia Syndrome Without Agraphia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alexia without agraphia", "shortest_name_length": 11}
{"curie": "UMLS:C1879904", "names": ["Burn From Lead", "Burns From Lead", "Burn From Leads", "Burns From Leads"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Burn From Lead", "shortest_name_length": 14}
{"curie": "UMLS:C1697980", "names": ["rectal necrosis", "Rectal necrosis", "Necrosis of rectum", "Rectal Necrotic Lesion", "rectal necrosis (diagnosis)", "Necrosis of rectum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rectal Necrotic Lesion", "shortest_name_length": 15}
{"curie": "UMLS:C2981383", "names": ["secondary central nervous system lymphoma", "Secondary Central Nervous System Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary Central Nervous System Lymphoma", "shortest_name_length": 41}
{"curie": "MONDO:0002791", "names": ["Large Cell Medulloblastoma", "Anaplastic medulloblastoma", "Large cell medulloblastoma", "large cell medulloblastoma", "large cell medulloblastoma (morphologic abnormality)", "Large cell medulloblastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "large cell medulloblastoma", "shortest_name_length": 26}
{"curie": "MONDO:0024282", "names": ["mucinous ovarian cancer", "Malignant Ovarian Mucinous Tumor", "malignant ovarian mucinous tumor", "malignant ovarian mucinous neoplasm", "Malignant Ovarian Mucinous Neoplasm", "ovarian mucinous neoplasm, malignant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucinous ovarian cancer", "shortest_name_length": 23}
{"curie": "MONDO:0011064", "names": ["lethal chondrodysplasia seller type", "lethal chondrodysplasia, Seller type", "CHONDRODYSPLASIA, LETHAL, WITH LONG BONE ANGULATION AND MIXED BONE DENSITY", "chondrodysplasia, lethal, with long bone angulation and mixed bone density", "Chondrodysplasia, Lethal, with Long Bone Angulation and Mixed Bone Density"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal chondrodysplasia, Seller type", "shortest_name_length": 35}
{"curie": "UMLS:C1514246", "names": ["Postradiation Breast Angiosarcoma", "Post-Radiotherapy Breast Angiosarcoma", "Postradiation Angiosarcoma of the Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postradiation Breast Angiosarcoma", "shortest_name_length": 33}
{"curie": "MONDO:0004353", "names": ["Extrahepatic Bile Duct IPN", "extrahepatic biliary papillomatosis", "Extrahepatic Biliary Papillomatosis", "Extrahepatic Bile Duct Papillomatosis", "extrahepatic bile duct papillomatosis", "papillomatosis of extrahepatic bile duct", "Extrahepatic Bile Duct Papillary Neoplasm", "extrahepatic bile duct papillary neoplasm", "papillomatosis of extrahepatic bile duct (diagnosis)", "Extrahepatic Bile Duct Intraductal Papillary Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extrahepatic biliary papillomatosis", "shortest_name_length": 26}
{"curie": "MONDO:0033310", "names": ["JBTS31", "JOUBERT SYNDROME 31", "Joubert syndrome 31"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome 31", "shortest_name_length": 6}
{"curie": "UMLS:C5206463", "names": ["Metastatic Malignant Female Reproductive System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Malignant Female Reproductive System Neoplasm", "shortest_name_length": 56}
{"curie": "MONDO:0018458", "names": ["HHC", "FFH", "FHH", "FBH", "FBHH", "FHH1", "FBH1", "HHC1", "FHH type 1", "hypocalciuric hypercalcemia", "Familial benign hypercalcemia", "familial benign hypercalcemia", "Familial Benign Hypercalcemia", "Familial benign hypercalcaemia", "HYPERCALCEMIA, FAMILIAL BENIGN", "Hypercalcemia, Familial Benign", "Familial Benign Hypercalcemia 1", "FAMILIAL BENIGN HYPERCALCEMIA 1", "familial hypocalciuric hypercalcemia", "Familial hypocalciuric hypercalcemia", "Familial Hypocalciuric Hypercalcemia", "Familial benign hypercalcemia type 1", "Familial hypocalciuric hypercalcaemia", "Hypercalcemia, familial benign type 1", "FHH - Familial hypocalciuric hypercalcemia", "Familial benign hypocalciuric hypercalcemia", "Familial hypocalciuric hypercalcemia type 1", "familial hypocalciuric hypercalcemia type I", "familial benign hypocalciuric hypercalcemia", "FHH - Familial hypocalciuric hypercalcaemia", "HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE I", "Hypocalciuric Hypercalcemia, Familial, Type I", "Hypocalciuric hypercalcemia, familial, type 1", "Familial hypocalciuric hypercalcemia syndrome", "Familial hypocalciuric hypercalcemia (disorder)", "familial hypocalciuric hypercalcemia (diagnosis)", "familial hypocalciuric hypercalcemia type I (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial hypocalciuric hypercalcemia", "shortest_name_length": 3}
{"curie": "MONDO:0013322", "names": ["FAME3", "FCMTE3", "familial adult myoclonic epilepsy 3", "EPILEPSY, FAMILIAL ADULT MYOCLONIC, 3", "epilepsy, familial ADULT myoclonic, 3", "epilepsy, familial adult myoclonic, 3", "Epilepsy, Familial Adult Myoclonic, 3", "familial cortical myoclonic tremor and epilepsy 3", "cortical myoclonic tremor with epilepsy, familial, 3", "CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, familial adult myoclonic, 3", "shortest_name_length": 5}
{"curie": "MONDO:0012734", "names": ["SERKAL", "SERKAL SYNDROME", "SERKAL Syndrome", "SERKAL syndrome", "Sex reversion-kidneys, adrenal and lung dysgenesis syndrome", "Sex reversion, kidney, adrenal and lung dysgenesis syndrome", "46,XX Sex reversal with dysgenesis of kidneys Adrenals and lungs", "46,XX Sex Reversal with Dysgenesis of Kidneys Adrenals and Lungs", "46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS", "46,XX SEX reversal with dysgenesis of kidneys, ADRENALS, and lungs", "46,XX Sex Reversal with Dysgenesis of Kidneys, Adrenals, and Lungs", "SERKAL (sex reversion, kidney, adrenal and lung dysgenesis) syndrome", "Sex Reversal, Female, With Dysgenesis Of Kidneys, Adrenals, And Lungs", "Sex reversion, kidney, adrenal and lung dysgenesis syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SERKAL syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C0521546", "names": ["anomaly; joint", "joint; anomaly", "Joint malformation", "JOINT MALFORMATION", "Congenital anomaly of joint", "deformity; joint, congenital", "joint; deformity, congenital", "Congenital joint malformation", "Congenital anomaly of joint, NOS", "Congenital articular malformation", "Congenital joint malformation NOS", "Congenital joint malformation, NOS", "Congenital anomaly of joint (disorder)", "Congenital articular malformation, NOS", "Congenital anomaly of joint (diagnosis)", "congenital malformations musculoskeletal system joint"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital anomaly of joint", "shortest_name_length": 14}
{"curie": "UMLS:C5556808", "names": ["Recurrent Primary Systemic Anaplastic Large Cell Lymphoma, ALK-Positive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Primary Systemic Anaplastic Large Cell Lymphoma, ALK-Positive", "shortest_name_length": 71}
{"curie": "MONDO:0008858", "names": ["BEHRS", "Behr Syndrome", "Behr syndrome", "BEHR SYNDROME", "behr syndrome", "behr's syndrome", "Behr syndrome 2", "Behr's syndrome", "Behr's syndrome I", "OPTIC ATROPHY, INFANTILE", "Behr syndrome (diagnosis)", "Abortive cerebellar ataxia", "OPTIC ATROPHY-ATAXIA SYNDROME", "optic atrophy-ataxia syndrome", "Infantile optic atrophy-ataxia", "Abortive cerebellar ataxia (BEHRS)", "infantile optic atrophy-ataxia syndrome", "optic atrophy, infantile hereditary, Behr complicated form of", "Optic atrophy, infantile hereditary, Behr complicated form of", "Optic Atrophy, Infantile Hereditary, With Neurologic Abnormalities", "OPTIC ATROPHY, INFANTILE HEREDITARY, WITH NEUROLOGIC ABNORMALITIES", "optic atrophy, infantile hereditary, with neurologic abnormalities", "optic atrophy in early childhood, associated with ataxia, spasticity, mental retardation, and posterior column sensory loss", "optic atrophy in early childhood, associated with ataxia, spasticity, intellectual disability, and posterior column sensory loss"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Behr syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C1880167", "names": ["Inherited Abnormalities of Erythrocyte Differentiation or Function", "Congenital Abnormalities of Erythrocyte Differentiation or Function"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Abnormalities of Erythrocyte Differentiation or Function", "shortest_name_length": 66}
{"curie": "MONDO:0002952", "names": ["follicular basal cell carcinoma", "Follicular Basal Cell Carcinoma", "Follicular basal cell carcinoma", "basal cell carcinoma, follicular", "Basal cell carcinoma - follicular", "skin follicular basal cell carcinoma", "Skin Follicular Basal Cell Carcinoma", "follicular (pilar) basal cell carcinoma", "basal cell carcinoma, follicular (diagnosis)", "Basal cell carcinoma - follicular (disorder)", "malignant neoplasm carcinoma basal cell follicular", "Skin Basal Cell Carcinoma with Matrical Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "follicular basal cell carcinoma", "shortest_name_length": 31}
{"curie": "OMIM:110700", "names": ["PLASMODIUM VIVAX, RESISTANCE TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 31}
{"curie": "UMLS:C2607933", "names": ["Malignant Coccygeal Body Tumor", "Malignant Glomus Coccygeum Tumor", "Malignant Coccygeal Body Neoplasm", "malignant tumor of coccygeal body", "Malignant Tumor of Coccygeal Body", "Malignant Glomus Coccygeum Neoplasm", "Malignant Neoplasm of Coccygeal Body", "malignant neoplasm of coccygeal body", "Malignant neoplasm of coccygeal body", "Malignant Tumor of the Coccygeal Body", "Malignant Neoplasm of the Coccygeal Body", "malignant neoplasm of coccygeal body (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Coccygeal Body Neoplasm", "shortest_name_length": 30}
{"curie": "MONDO:0014191", "names": ["CPVT5", "CVPT5", "CARDAR", "TRIADEN KNOCKOUT SYNDROME", "catecholaminergic polymorphic ventricular tachycardia 5", "TRDN catecholaminergic polymorphic ventricular tachycardia", "catecholaminergic polymorphic ventricular tachycardia type 5", "CARDIAC ARRHYTHMIA SYNDROME WITH OR WITHOUT SKELETAL MUSCLE WEAKNESS", "cardiac arrhythmia syndrome, with or without skeletal muscle weakness", "CARDIAC ARRHYTHMIA SYNDROME, WITH OR WITHOUT SKELETAL MUSCLE WEAKNESS", "catecholaminergic polymorphic ventricular tachycardia caused by mutation in TRDN", "VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 5, WITH OR WITHOUT MUSCLE WEAKNESS", "ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "catecholaminergic polymorphic ventricular tachycardia 5", "shortest_name_length": 5}
{"curie": "UMLS:C2204355", "names": ["Salivary Gland Diffuse Large B-Cell Lymphoma", "large B-cell diffuse lymphoma of salivary gland", "Primary Salivary Gland Diffuse Large B-Cell Lymphoma", "large B-cell diffuse lymphoma of salivary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "large B-cell diffuse lymphoma of salivary gland", "shortest_name_length": 44}
{"curie": "UMLS:C4552325", "names": ["CSF HIV escape syndrome", "Cerebrospinal fluid HIV escape syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebrospinal fluid HIV escape syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0011938", "names": ["ASD2", "atrial septal defect 2", "ATRIAL SEPTAL DEFECT 2", "Atrial septal defect 2", "atrial septal defect type 2", "atrial heart septal defect 2", "atrial septal defect 2 - ASD2", "GATA4 atrial heart septal defect", "atrial heart septal defect type 2", "atrial septal defect 2 - ASD2 (diagnosis)", "atrial heart septal defect caused by mutation in GATA4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial septal defect 2", "shortest_name_length": 4}
{"curie": "MONDO:0003258", "names": ["Hobnail Hemangioma", "hobnail hemangioma", "Targetoid Hemosiderotic Hemangioma", "Targetoid Hemosiderotic hemangioma", "Targetoid hemosiderotic hemangioma", "Targetoid haemosiderotic hemangioma", "Targetoid haemosiderotic haemangioma", "Targetoid hemosiderotic hemangioma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hobnail hemangioma", "shortest_name_length": 18}
{"curie": "MONDO:0003522", "names": ["male orgasm disorder", "inhibited male orgasm", "Inhibited male orgasm", "Male orgasmic disorder", "male Orgasmic disorder", "male orgasmic disorder", "Male Orgasmic Disorder", "male orgasmic disorder inhibited", "Inhibited male orgasm (disorder)", "inhibited male orgasmic disorder", "male orgasmic disorder (diagnosis)", "inhibited male orgasmic disorder (diagnosis)", "Psychosexual dysfunction with inhibited male orgasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "male orgasm disorder", "shortest_name_length": 20}
{"curie": "MONDO:0010149", "names": ["Tcn2 deficiency", "TCN2 DEFICIENCY", "TCN2 deficiency", "TC 2 deficiency", "TC II DEFICIENCY", "Transcobalamin deficiency", "transcobalamin deficiency", "transcobalamin 2 deficiency", "TRANSCOBALAMIN II DEFICIENCY", "transcobalamin II deficiency", "Transcobalamin II Deficiency", "transcobalamin ii deficiency", "Transcobalamin II deficiency", "transcobalamin II; deficiency", "deficiency; transcobalamin II", "TCN2 - Transcobalamin II deficiency", "Inherited deficiency of transcobalamin", "inherited deficiency of transcobalamin", "Transcobalamin II deficiency (disorder)", "transcobalamin II deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transcobalamin II deficiency", "shortest_name_length": 15}
{"curie": "MONDO:0021325", "names": ["thoracic part of esophagus cancer", "cancer of thoracic part of esophagus", "malignant tumor of thoracic esophagus", "malignant neoplasm of thoracic esophagus", "Malignant neoplasm of thoracic esophagus", "Malignant Neoplasm of Thoracic Esophagus", "Malignant neoplasm of thoracic oesophagus", "Malignant Neoplasm of the Thoracic Esophagus", "malignant neoplasm of the thoracic esophagus", "malignant thoracic part of esophagus neoplasm", "Malignant tumor of thoracic part of esophagus", "Malignant tumour of thoracic part of oesophagus", "malignant neoplasm of thoracic part of esophagus", "Malignant neoplasm of thoracic part of esophagus", "Malignant neoplasm of thoracic part of oesophagus", "malignant neoplasm of thoracic esophagus (diagnosis)", "Malignant tumor of thoracic part of esophagus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant neoplasm of thoracic esophagus", "shortest_name_length": 33}
{"curie": "UMLS:C1334755", "names": ["Microinvasive Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Microinvasive Malignant Neoplasm", "shortest_name_length": 32}
{"curie": "UMLS:C4331340", "names": ["Stage IVA Unknown Primary Tumor (Except for EBV-Related and HPV-Related Tumors) and Metastatic Cervical Adenopathy AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Unknown Primary Tumor (Except for EBV-Related and HPV-Related Tumors) and Metastatic Cervical Adenopathy AJCC v8", "shortest_name_length": 122}
{"curie": "MONDO:0022094", "names": ["Cartwright Nelson Fryns syndrome", "Growth retardation, severe mental retardation, acral limb deficiencies with poorly keratinized nails", "Growth retardation, severe intellectual disability, acral limb deficiencies with poorly keratinized nails"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cartwright Nelson Fryns syndrome", "shortest_name_length": 32}
{"curie": "MONDO:0010671", "names": ["MCOPS4", "MCOPS1", "MAA, formerly", "Lenz Syndrome", "MAA, FORMERLY", "LENZ DYSPLASIA", "Lenz dysplasia", "Lenz syndrome 2", "ANOP1, formerly", "ANOP1, FORMERLY", "MCOPS4, formerly", "MCOPS4, FORMERLY", "Lenz microphthalmia", "Lenz type microphthalmia", "Microphthalmia, Lenz type", "syndromic microphthalmia 4", "syndromic microphthalmia 1", "microphthalmia syndromic 4", "Microphthalmia, Syndromic 4", "MICROPHTHALMIA, SYNDROMIC 1", "Microphthalmia, syndromic 1", "microphthalmia, syndromic 1", "LENZ MICROPHTHALMIA SYNDROME", "Lenz dysmorphogenic syndrome", "Lenz microphthalmia syndrome", "Lenz Dysmorphogenic Syndrome", "syndromic microphthalmia type 4", "Syndromic microphthalmia type 4", "microphthalmia, syndromic type 1", "MICROPHTHALMIA, SYNDROMIC 4, FORMERLY", "microphthalmia, syndromic 4, formerly", "MICROPHTHALMIA, SYNDROMIC 4 (disorder)", "Lenz microphthalmia syndrome (disorder)", "Microphthalmia Or Anophthalmos with Associated Anomalies", "microphthalmia or anophthalmos with associated anomalies", "Microphthalmia With Ankyloblepharon And Mental Retardation", "microphthalmia with ankyloblepharon and mental retardation", "microphthalmia or anophthalmos with associated anomalies (MAA)", "microphthalmia with ankyloblepharon and intellectual disability", "Microphthalmia-ankyloblepharon-intellectual disability syndrome", "Microphthalmia or anophthalmos with associated anomalies (formerly)", "Microphthalmia with ankyloblepharon and intellectual disability syndrome", "microphthalmia with ankyloblepharon and intellectual disability syndrome", "Microphthalmia with ankyloblepharon and intellectual disability syndrome (disorder)", "microphthalmia with ankyloblepharon and intellectual disability syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microphthalmia, syndromic 1", "shortest_name_length": 6}
{"curie": "UMLS:C1504419", "names": ["Pelvic bleeding", "Pelvic Bleeding", "Pelvic Hemorrhage", "Pelvic hemorrhage", "Pelvic haemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pelvic hemorrhage", "shortest_name_length": 15}
{"curie": "MONDO:0013463", "names": ["DTGA3", "CHTD6", "DTGA3, FORMERLY", "CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 6", "congenital heart defects, multiple types, 6", "multiple types of congenital heart defects 6", "dextro-looped transposition of the great arteries 3", "transposition of the great arteries, dextro-looped 3", "GDF1 dextro-looped transposition of the great arteries", "dextro-looped transposition of the great arteries type 3", "transposition of the great arteries, dextro-looped type 3", "TRANSPOSITION OF THE GREAT ARTERIES, DEXTRO-LOOPED 3, FORMERLY", "transposition of the great arteries, dextro-looped 3, formerly", "dextro-looped transposition of the great arteries caused by mutation in GDF1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital heart defects, multiple types, 6", "shortest_name_length": 5}
{"curie": "MONDO:0021157", "names": ["GC cervicitis", "gonorrhea cervix", "cervix; gonorrhea", "gonorrhea; cervix", "gonorrhea of cervix", "Gonorrhea of cervix", "gonococcal cervicitis", "Cervicitis gonococcal", "Cervicitis;gonococcal", "Gonococcal cervicitis", "CERVICITIS GONOCOCCAL", "gonococcal; cervicitis", "cervicitis; gonococcal", "Cervicitis gonococcal NOS", "gonorrhea of uterine cervix", "Gonococcal cervicitis (disorder)", "gonococcal cervicitis (diagnosis)", "Gonococcal cervicitis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gonococcal cervicitis", "shortest_name_length": 13}
{"curie": "UMLS:C4054575", "names": ["Mammary-Type Myofibroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mammary-Type Myofibroblastoma", "shortest_name_length": 29}
{"curie": "MONDO:0000527", "names": ["adenoma colon", "Colon Adenoma", "Adenoma;colon", "colon adenoma", "Colon adenoma", "adenomas colon", "colonic adenoma", "Colonic Adenoma", "Adenoma of Colon", "adenoma of colon", "Colonic adenomas", "Adenoma of the Colon", "adenoma of the colon", "Colon Adenomatous Polyp", "Colon adenomatous polyp", "COLON, ADENOMATOUS POLYP", "adenomatous colon polyps", "Colonic Adenomatous Polyp", "Adenomatous polyps, colon", "Adenomatous polyp of colon", "Adenomatous Polyp of Colon", "Adenomatous colonic polyps", "COLON NOS POLYP ADENOMATOUS", "Adenomatous Polyp of the Colon", "Adenomatous polyp of colon (disorder)", "colon (non-specific) polyp adenomatous"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colon adenoma", "shortest_name_length": 13}
{"curie": "UMLS:C1334697", "names": ["Meningioma by Site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meningioma by Site", "shortest_name_length": 18}
{"curie": "UMLS:C4744548", "names": ["Metastatic Esophageal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Esophageal Carcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C5555191", "names": ["Refractory Primary Peritoneal Undifferentiated Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Primary Peritoneal Undifferentiated Carcinoma", "shortest_name_length": 56}
{"curie": "MONDO:0004743", "names": ["Homocysteinemia", "homocysteinemia", "Homocysteinaemia", "Hyperhomocysteinemia", "hyperhomocysteinemia", "HYPERHOMOCYSTEINEMIA", "hyperhomocysteinaemia", "Hyperhomocysteinaemia", "Hyperhomocysteinemias", "homocysteinemia (diagnosis)", "Hyperhomocysteinemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperhomocysteinemia", "shortest_name_length": 15}
{"curie": "MONDO:0007882", "names": ["LATTICE DEGENERATION OF RETINA LEADING TO RETINAL DETACHMENT", "Lattice Degeneration of Retina Leading to Retinal Detachment", "lattice degeneration of retina leading to retinal detachment"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lattice degeneration of retina leading to retinal detachment", "shortest_name_length": 60}
{"curie": "MONDO:0013989", "names": ["DEE14", "EIEE14", "early infantile epileptic encephalopathy 14", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14", "Epileptic Encephalopathy, Early Infantile, 14", "epileptic encephalopathy, early infantile, 14", "Developmental and Epileptic Encephalopathy 14", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 14", "developmental and epileptic encephalopathy 14", "KCNT1 early infantile epileptic encephalopathy", "developmental and epileptic encephalopathy, 14", "epileptic encephalopathy, early infantile, type 14", "early infantile epileptic encephalopathy caused by mutation in KCNT1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 14", "shortest_name_length": 5}
{"curie": "MONDO:0019662", "names": ["SRPS type 2", "short rib-polydactyly syndrome type 2", "short rib-polydactyly syndrome Majewski type", "short rib-polydactyly syndrome, Majewski type", "polydactyly with neonatal chondrodystrophy type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short rib-polydactyly syndrome, Majewski type", "shortest_name_length": 11}
{"curie": "UMLS:C5419741", "names": ["Advanced Kidney Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Kidney Carcinoma", "shortest_name_length": 25}
{"curie": "UMLS:C1868882", "names": ["Human herpesvirus 6 infection reactivation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Human herpesvirus 6 infection reactivation", "shortest_name_length": 42}
{"curie": "UMLS:C4080064", "names": ["Autosomal Dominant Hereditary Pancreatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Autosomal Dominant Hereditary Pancreatitis", "shortest_name_length": 42}
{"curie": "MONDO:0100006", "names": ["secondary MACS", "secondary mast cell activation syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary mast cell activation syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0001368", "names": ["phthisical cornea", "Phthisical cornea", "Phthisical cornea (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phthisical cornea", "shortest_name_length": 17}
{"curie": "UMLS:C2111725", "names": ["Kidney Large Cell Neuroendocrine Carcinoma", "large cell neuroendocrine carcinoma of kidney", "large cell neuroendocrine carcinoma of kidney (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "large cell neuroendocrine carcinoma of kidney", "shortest_name_length": 42}
{"curie": "UMLS:C1335115", "names": ["Mouth Adenocarcinoma", "Adenocarcinoma of Mouth", "Oral Cavity Adenocarcinoma", "Adenocarcinoma of the Mouth", "adenocarcinoma of oral cavity", "Adenocarcinoma of Oral Cavity", "Adenocarcinoma of the Oral Cavity", "adenocarcinoma of oral cavity (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenocarcinoma of oral cavity", "shortest_name_length": 20}
{"curie": "MONDO:0011535", "names": ["SHFM4", "split-hand/foot malformation 4", "SPLIT-HAND/FOOT MALFORMATION 4", "Split-Hand-Foot Malformation 4", "split hand-foot malformation 4", "TP63 split hand-foot malformation", "split-hand/foot malformation type 4", "split hand-foot malformation type 4", "split hand-foot malformation caused by mutation in TP63"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "split hand-foot malformation 4", "shortest_name_length": 5}
{"curie": "MONDO:0100394", "names": ["AML, t(1;22)", "acute myeloid leukemia, t(1;22)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, t(1;22)", "shortest_name_length": 12}
{"curie": "MONDO:0012444", "names": ["NBIA2B", "NBIA2b", "Karak syndrome", "Karak Syndrome", "KARAK SYNDROME", "atypical neuroaxonal dystrophy", "Neuroaxonal Dystrophy, Atypical", "NEUROAXONAL DYSTROPHY, ATYPICAL", "neuroaxonal dystrophy, atypical", "neurodegeneration with brain iron accumulation 2B", "NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B", "Neurodegeneration With Brain Iron Accumulation 2B", "neurodegeneration with brain iron accumulation 2b", "neurodegeneration with brain iron accumulation type 2b", "neurodegeneration with brain iron accumulation type 2B", "NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2 (disorder)", "NEURODEGENERATION WITH BRAIN IRON ACCUMULATION, PLA2G6-RELATED", "Neurodegeneration With Brain Iron Accumulation, Pla2g6-Related", "neurodegeneration with brain iron accumulation, Pla2g6-related", "Neurodegeneration With Brain Iron Accumulation, PLA2G6-Related", "neurodegeneration with brain iron accumulation, Pla2G6-related", "early-onset progressive cerebellar ataxia dystonia spasticity and intellectual decline"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodegeneration with brain iron accumulation 2B", "shortest_name_length": 6}
{"curie": "UMLS:C5555527", "names": ["Recurrent Acute Bilineal Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Acute Bilineal Leukemia", "shortest_name_length": 33}
{"curie": "MONDO:0020397", "names": ["parachute tricuspid valve"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parachute tricuspid valve", "shortest_name_length": 25}
{"curie": "MONDO:0011337", "names": ["HLH2", "FHL2", "Hlh2", "Hplh2", "HPLH2", "familial hemophagocytic lymphohistiocytosis 2", "HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2", "Hemophagocytic lymphohistiocytosis, familial, 2", "hemophagocytic lymphohistiocytosis, familial, 2", "PRF1 genetic hemophagocytic lymphohistiocytosis", "familial hemophagocytic lymphohistiocytosis type 2", "hemophagocytic lymphohistiocytosis, familial, type 2", "genetic hemophagocytic lymphohistiocytosis caused by mutation in PRF1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial hemophagocytic lymphohistiocytosis 2", "shortest_name_length": 4}
{"curie": "UMLS:C4683146", "names": ["Posterior Uveal Melanoma by AJCC v8 Stage", "Choroidal and Ciliary Body Melanoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Choroidal and Ciliary Body Melanoma by AJCC v8 Stage", "shortest_name_length": 41}
{"curie": "MONDO:0004456", "names": ["abuse cocaine", "COCAINE ABUSE", "Cocaine abuse", "cocaine abuse", "Cocaine Abuse", "cocaine; abuse", "Abuse, Cocaine", "abuse; cocaine", "Abuse;drug(s);cocaine", "abuse cocaine disorders", "Cocaine-Related Disorder", "Cocaine abuse (disorder)", "Disorder, Cocaine-Related", "cocaine abuse (diagnosis)", "cocaine-related disorders", "Cocaine Related Disorders", "Cocaine-Related Disorders", "Cocaine related disorders", "Disorders, Cocaine-Related", "Cocaine abuse, unspecified", "Cocaine-related disorder, NOS", "Cocaine abuse, unspecified use", "Cocaine induced mental disorder", "cocaine-related disorders (diagnosis)", "Cocaine-induced organic mental disorder", "Organic mental disorder caused by cocaine", "Cocaine-induced organic mental disorder, NOS", "Organic mental disorder caused by cocaine (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cocaine abuse", "shortest_name_length": 13}
{"curie": "UMLS:C4329703", "names": ["Defective Thyroglobulin Synthesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Defective Thyroglobulin Synthesis", "shortest_name_length": 33}
{"curie": "MONDO:0003222", "names": ["CNS Melanocytic Tumor", "CNS melanocytic tumor", "melanocytic tumor of CNS", "CNS melanocytic neoplasm", "Melanocytic Tumor of CNS", "CNS Melanocytic Neoplasm", "Melanocytic Neoplasm of CNS", "melanocytic neoplasm of CNS", "Melanocytic Tumor of the CNS", "melanocytic tumor of the CNS", "melanocytic neoplasm of the CNS", "Melanocytic Neoplasm of the CNS", "Primary Melanocytic Lesion of Meninges", "primary melanocytic lesions of the CNS", "Primary melanocytic lesion of meninges", "primary melanocytic lesion of meninges", "primary melanocytic Lesions of the CNS", "Central Nervous System Melanocytic Tumor", "central nervous system melanocytic tumor", "Central Nervous System Melanocytic Neoplasm", "Melanocytic Tumor of Central Nervous System", "melanocytic tumor of central nervous system", "central nervous system melanocytic neoplasm", "central nervous system melanocytic neoplasms", "Central Nervous System Melanocytic Neoplasms", "meningeal neoplasm primary melanocytic lesion", "melanocytic neoplasm of central nervous system", "Melanocytic Neoplasm of Central Nervous System", "Melanocytic Tumor of the Central Nervous System", "melanocytic tumor of the central nervous system", "central nervous system primary melanocytic lesion", "Primary melanocytic lesion of meninges (disorder)", "melanocytic neoplasm of the central nervous system", "Primary melanocytic lesion of meninges (diagnosis)", "Melanocytic Neoplasm of the Central Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system melanocytic neoplasm", "shortest_name_length": 21}
{"curie": "MONDO:0004453", "names": ["myxomatous pattern testicular yolk sac tumor", "Testicular Yolk Sac Tumor, Myxomatous Pattern", "testicular yolk sac tumor, myxomatous pattern"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular yolk sac tumor, myxomatous pattern", "shortest_name_length": 44}
{"curie": "UMLS:C0265031", "names": ["Bleeding pile", "bleeding piles", "Bleeding piles", "bleed hemorrhoids", "Bleeding hemorrhoid", "hemorrhoid bleeding", "HEMORRHOID BLEEDING", "bleeding hemorrhoid", "bleeding hemorrhoids", "BLEEDING HEMORRHOIDS", "Bleeding hemorrhoids", "hemorrhoids bleeding", "Bleeding haemorrhoid", "Hemorrhoidal bleeding", "bleeding hemorrhoidal", "Bleeding haemorrhoids", "hemorrhoidal bleeding", "bleeding haemorrhoids", "Haemorrhoidal bleeding", "Hemorrhoidal hemorrhage", "hemorrhage; hemorrhoids", "Bleeding of hemorrhoids", "hemorrhoids; hemorrhage", "Hemorrhoidal Hemorrhage", "hemorrhoids with bleeding", "Haemorrhoidal haemorrhage", "Hemorrhoids (bleeding) NOS", "Bleeding hemorrhoids (disorder)", "hemorrhoids with bleeding (diagnosis)", "Bleeding hemorrhoids, unspecified whether internal or external"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemorrhoidal Hemorrhage", "shortest_name_length": 13}
{"curie": "UMLS:C4682577", "names": ["Stage IVB Uterine Corpus Endometrial Stromal Sarcoma", "Stage IVB Uterine Corpus Endometrial Stromal Sarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Uterine Corpus Endometrial Stromal Sarcoma AJCC v8", "shortest_name_length": 52}
{"curie": "MONDO:0011628", "names": ["prop", "PCC Deficiency", "PCC deficiency", "Deficiency, PCC", "PCC Deficiencies", "Deficiencies, PCC", "Propionicaciduria", "Propionicacidemia", "Ketotic glycinemia", "Propionic Aciduria", "PROPIONIC ACIDEMIA", "Propionicacidurias", "ketotic glycinemia", "Acidemia Propionic", "Propionicacidemias", "propionic aciduria", "Propionic aciduria", "propionic acidemia", "Ketotic Glycinemia", "Propionic acidemia", "Propionic Acidemia", "GLYCINEMIA, KETOTIC", "Propionic Acidurias", "Propionic Acidemias", "Acidemia, Propionic", "Propionic acidaemia", "propionic; acidemia", "Ketotic glycinaemia", "Aciduria, Propionic", "Glycinemia, ketotic", "GLYCINEMIA, ketotic", "acidemia; propionic", "Glycinemia, Ketotic", "Acidemia Propionics", "propionic acidaemia", "Propionic, Acidemia", "Ketotic Glycinemias", "Acidurias, Propionic", "Propionics, Acidemia", "Glycinemias, Ketotic", "Acidemias, Propionic", "ketotic II glycinemia", "Ketotic hyperglycinemia", "ketotic hyperglycinemia", "KETOTIC HYPERGLYCINEMIA", "Ketotic Hyperglycinemia", "Propionic acidemia, NOS", "Ketotic Hyperglycinemias", "ketotic hyperglycinaemia", "Ketotic hyperglycinaemia", "Hyperglycinemia, Ketotic", "Hyperglycinemias, Ketotic", "disorder; propionic acidemia", "propionic acidemia; disorder", "Hyperglycinemia, ketotic form", "Propionic acidemia (disorder)", "propionic acidemia (diagnosis)", "propionyl coA carboxylase deficiency", "Propionyl CoA Carboxylase Deficiency", "propionyl-CoA carboxylase deficiency", "Propionyl-CoA carboxylase deficiency", "propionyl-Coa carboxylase deficiency", "Propionyl-CoA Carboxylase Deficiency", "Carboxylase Deficiency, Propionyl-CoA", "Deficiency, Propionyl-CoA Carboxylase", "Propionyl-CoA Carboxylase Deficiencies", "Deficiencies, Propionyl-CoA Carboxylase", "Carboxylase Deficiencies, Propionyl-CoA", "PCC - Propionyl-CoA carboxylase deficiency", "Hyperglycinemia with ketosis and leukopenia", "Hyperglycinemia with ketosis and leucopenia", "Hyperglycinaemia with ketosis and leucopenia", "Hyperglycinemia With Ketoacidosis And Leukopenia", "hyperglycinemia with ketoacidosis and leukopenia", "HYPERGLYCINEMIA WITH KETOACIDOSIS AND LEUKOPENIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "propionic acidemia", "shortest_name_length": 4}
{"curie": "UMLS:C0441713", "names": ["Chemical Injury", "Chemical injury", "chemical injury", "injury chemical", "Chemical injuries", "Chemical injury NOS", "Chemical injury (qualifier value)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chemical injury", "shortest_name_length": 15}
{"curie": "MONDO:0015781", "names": ["Seaver-Cassidy syndrome", "Seaver Cassidy syndrome", "Seaver Cassidy syndrome (disorder)", "facial dysmorphism shawl scrotum joint laxity", "facial dysmorphism-shawl scrotum-joint laxity syndrome", "Facial dysmorphism-shawl scrotum-joint laxity syndrome", "hypertelorism, downslanting palpebral fissures, malar hypoplasia, and apparently low-set ears associated with joint and scrotal anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "facial dysmorphism-shawl scrotum-joint laxity syndrome", "shortest_name_length": 23}
{"curie": "UMLS:C1334015", "names": ["High Grade Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Intraepithelial Neoplasia", "shortest_name_length": 36}
{"curie": "MONDO:0014781", "names": ["COXPD29", "combined oxidative phosphorylation deficiency 29", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29", "Combined oxidative phosphorylation defect type 29", "TXN2 combined oxidative phosphorylation deficiency", "combined oxidative phosphorylation deficiency type 29", "combined oxidative phosphorylation deficiency 29; COXPD29", "COXPD29 - combined oxidative phosphorylation defect type 29", "Combined oxidative phosphorylation defect type 29 (disorder)", "combined oxidative phosphorylation deficiency caused by mutation in TXN2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation deficiency 29", "shortest_name_length": 7}
{"curie": "MONDO:0010663", "names": ["JMS", "SFMS", "SFM1", "MRXHF1", "Chudley syndrome 1", "HOLMES-GANG SYNDROME", "Holmes Gang syndrome", "Holmes-Gang syndrome", "Chudley-Lowry Syndrome", "CHUDLEY-LOWRY SYNDROME", "Chudley-Lowry syndrome", "Juberg-Marsidi syndrome", "Juberg Marsidi syndrome", "Carpenter Waziri syndrome", "CARPENTER-WAZIRI SYNDROME", "Carpenter-Waziri syndrome", "Chudley-Lowry-Hoar syndrome", "Chudley Lowry Hoar syndrome", "Smith-Fineman-Myers syndrome", "Smith Fineman Myers syndrome", "SMITH-FINEMAN-MYERS SYNDROME 1", "XLMR-hypotonic facies syndrome", "Smith Fineman Myers syndrome 1", "XLMR-HYPOTONIC FACIES SYNDROME", "Smith-fineman-myers syndrome 1", "Smith-Fineman-Myers syndrome (SFMS)", "Chudley mental retardation syndrome", "Chudley-Lowry-Hoar syndrome (diagnosis)", "Chudley intellectual disability syndrome", "Juberg-Marsidi mental retardation syndrome", "Mental retardation Smith Fineman Myers type", "mental retardation Smith Fineman Myers type", "intellectual disability Smith Fineman Myers type", "X-linked hypogonadism gynecomastia mental retardation", "X-Linked Mental Retardation-Hypotonic Facies Syndrome", "X-linked mental retardation-hypotonic facies syndrome-1", "mental retardation-hypotonic facies syndrome X-linked, 1", "X-linked intellectual disability hypotonic face syndrome", "X-linked intellectual disability-hypotonic face syndrome", "Mental retardation-hypotonic facies syndrome, x-linked, 1", "mental retardation-hypotonic facies syndrome, X-linked, 1", "MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1", "X-linked hypogonadism gynecomastia intellectual disability", "intellectual disability-hypotonic facies syndrome X-linked, 1", "INTELLECTUAL DISABILITY-HYPOTONIC FACIES SYNDROME, X-LINKED, 1", "mental retardation-hypotonic facies syndrome, X-linked, type 1", "intellectual disability-hypotonic facies syndrome, X-linked, 1", "intellectual disability-hypotonic facies syndrome, X-linked, type 1", "X-linked intellectual disability hypotonic face syndrome (disorder)", "X-linked intellectual disability hypotonic face syndrome (diagnosis)", "mental retradation, X-linked with Growth delay, deafness, microgenitalism", "Mental Retradation, X-linked with Growth Delay, Deafness, Microgenitalism", "mental retardation-hypotonic facies syndrome, X-linked, X-linked recessive", "Mental retardation, x-linked, with growth retardation, deafness, and microgenitalism", "mental retardation, X-linked, with growth retardation, deafness, and microgenitalism", "intellectual disability, X-linked, with growth retardation, deafness, and microgenitalism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability-hypotonic facies syndrome, X-linked, 1", "shortest_name_length": 3}
{"curie": "MONDO:0000600", "names": ["nosophobia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nosophobia", "shortest_name_length": 10}
{"curie": "MONDO:0004627", "names": ["DUODENITIS", "duodenitis", "Duodenitis", "duodenitis nos", "Duodenitis, NOS", "Duodenal inflammation", "Duodenitis (disorder)", "duodenum inflammation", "hemorrhagic duodenitis", "duodenum; inflammation", "inflammation; duodenum", "duodenitis (diagnosis)", "Hemorrhagic duodenitis", "inflammation of duodenum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "duodenitis", "shortest_name_length": 10}
{"curie": "UMLS:C0275555", "names": ["acute bacterial epiglottis", "Acute bacterial epiglottitis", "epiglottitis acute, bacterial", "acute bacterial epiglottis (diagnosis)", "Acute bacterial epiglottitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute bacterial epiglottitis", "shortest_name_length": 26}
{"curie": "MONDO:0015144", "names": ["brain inflammation", "inflammation of brain", "brain inflammatory disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brain inflammatory disease", "shortest_name_length": 18}
{"curie": "UMLS:C0850327", "names": ["Carcinoma;cervix;undifferentia", "Undifferentiated Cervical Cancer", "Cervical Carcinoma, Unclassifiable", "Cervical Undifferentiated Carcinoma", "undifferentiated carcinoma of cervix", "undifferentiated carcinoma of the cervix", "undifferentiated carcinoma of cervix (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "undifferentiated carcinoma of cervix", "shortest_name_length": 30}
{"curie": "MONDO:0010893", "names": ["MHS4", "Mhs4", "malignant hyperthermia susceptibility 4", "malignant hyperthermia, susceptibility to, 4", "MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 4", "malignant hyperpyrexia susceptibility type 4", "Malignant hyperthermia susceptibility type 4", "Malignant hyperpyrexia susceptibility type 4", "malignant hyperthermia susceptibility type 4", "malignant hyperthermia, susceptibility to, type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant hyperthermia, susceptibility to, 4", "shortest_name_length": 4}
{"curie": "MONDO:0010623", "names": ["RUDS", "Ruds", "Rud syndrome", "rud syndrome", "Rud Syndrome", "RUD SYNDROME", "Rud's syndrome", "Rud's syndrome (disorder)", "Linear nevus-convulsion syndrome", "Ichthyosis and male hypogonadism", "ichthyosis and male hypogonadism", "ICHTHYOSIS AND MALE HYPOGONADISM", "neuroichthyosis-hypogonadism syndrome", "Neuroichthyosis hypogonadism syndrome", "Ichthyosis male hypogonadism syndrome", "ichthyosis-male hypogonadism syndrome", "Ichthyosis-male hypogonadism syndrome", "ichthyosis-oligophrenia-epilepsy syndrome", "Ichthyosis oligophrenia epilepsy syndrome", "Ichthyosis mental retardation-epilepsy hypogonadism syndrome", "ichthyosis-mental retardation-epilepsy-hypogonadism syndrome", "Ichthyosis hypogonadism mental retardation epilepsy syndrome", "ichthyosis-hypogonadism-mental retardation-epilepsy syndrome", "Dwarfism ichthyosiform erythroderma mental deficiency syndrome", "dwarfism-ichthyosiform erythroderma-mental deficiency syndrome", "Dwarfism-ichthyosiform erythroderma-mental deficiency syndrome", "Ichthyosis, bilateral cryptorchidism, hypogenitalism and mental retardation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ichthyosis and male hypogonadism", "shortest_name_length": 4}
{"curie": "UMLS:C4521906", "names": ["Stage III Hepatocellular Cancer", "Stage III Hepatocellular Carcinoma", "Stage III Hepatocellular Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Hepatocellular Carcinoma AJCC v7", "shortest_name_length": 31}
{"curie": "MONDO:0003911", "names": ["Ciliary Body Mixed Cell Melanoma", "ciliary body mixed cell melanoma", "ciliary body mixed cell uveal melanoma", "mixed cell uveal melanoma of ciliary body"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ciliary body mixed cell melanoma", "shortest_name_length": 32}
{"curie": "MONDO:0030338", "names": ["ANPH2", "ANENCEPHALY 2", "anencephaly 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anencephaly 2", "shortest_name_length": 5}
{"curie": "UMLS:C4288927", "names": ["IFN-gamma Receptor 1 Deficiency", "IFN-gamma receptor 1 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IFN-gamma Receptor 1 Deficiency", "shortest_name_length": 31}
{"curie": "MONDO:0034846", "names": ["primary desmosis coli"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary desmosis coli", "shortest_name_length": 21}
{"curie": "MONDO:0011330", "names": ["Sca10", "SCA10", "spinocerebellar ataxia 10", "SPINOCEREBELLAR ATAXIA 10", "Spinocerebellar Ataxia 10", "Spinocerebellar ataxia type 10", "spinocerebellar ataxia type 10", "SCA10 Spinocerebellar Ataxia 10", "Spinocerebellar ataxia type 10 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia type 10", "shortest_name_length": 5}
{"curie": "MONDO:0017264", "names": ["syndromic RXLI", "Syndromic RXLI", "syndromic X-linked ichthyosis", "Syndromic X-linked ichthyosis", "syndromic recessive X-linked ichthyosis", "Syndromic recessive X-linked ichthyosis", "Syndromic recessive X-linked ichthyosis (disorder)", "syndrome associated with recessive X-linked ichthyosis", "recessive X-linked ichthyosis with extracutaneous manifestations", "Recessive X-linked ichthyosis with extracutaneous manifestations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic recessive X-linked ichthyosis", "shortest_name_length": 14}
{"curie": "MONDO:0009195", "names": ["erythema of acral regions", "ERYTHEMA OF ACRAL REGIONS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythema of acral regions", "shortest_name_length": 25}
{"curie": "MONDO:0024481", "names": ["skin; appendage", "skin appendage disorder", "disorder of skin appendage", "Disorder of skin appendage", "cutaneous appendage disease", "Disorders of skin appendages", "SKIN AND APPENDAGES DISORDERS", "disease of epidermal appendage", "disease of cutaneous appendage", "Disease of epidermal appendage", "Disease of epidermal appendages", "disorder of cutaneous appendage", "disease of epidermal appendages", "DISEASES OF THE EPIDERMAL APPENDAGES", "Disorder of skin appendage (disorder)", "disorder of skin appendage (diagnosis)", "Disorders of skin appendages (L60-L75)", "cutaneous appendage disease or disorder", "disease or disorder of cutaneous appendage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin appendage disorder", "shortest_name_length": 15}
{"curie": "MONDO:0036193", "names": ["PKNPY", "PARKINSONISM WITH POLYNEUROPATHY", "parkinsonism with polyneuropathy", "Parkinsonism with polyneuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parkinsonism with polyneuropathy", "shortest_name_length": 5}
{"curie": "UMLS:C1334047", "names": ["HHV-8 Related Malignancy", "HHV-8-Related Malignancy", "HHV8-Related Malignant Neoplasm", "Human Herpes Virus 8 Related Malignancy", "Human Herpes Virus 8-Related Malignancy", "Human Herpes Virus 8-Related Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HHV8-Related Malignant Neoplasm", "shortest_name_length": 24}
{"curie": "UMLS:C4724995", "names": ["Recurrent Paranasal Sinus Squamous Cell Cancer", "Recurrent Paranasal Sinus Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Paranasal Sinus Squamous Cell Carcinoma", "shortest_name_length": 46}
{"curie": "UMLS:C3203550", "names": ["Exposure via father"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Exposure via father", "shortest_name_length": 19}
{"curie": "MONDO:0014745", "names": ["CMS19", "congenital myasthenic syndrome 19", "myasthenic syndrome, congenital, 19", "MYASTHENIC SYNDROME, CONGENITAL, 19", "congenital myasthenic syndrome type 19", "COL13A1 congenital myasthenic syndrome", "myasthenic syndrome, congenital, type 19", "congenital myasthenic syndrome caused by mutation in COL13A1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myasthenic syndrome 19", "shortest_name_length": 5}
{"curie": "MONDO:0005684", "names": ["BULBAR POLIO", "bulbar polio", "Bulbar Polio", "Bulbar polio", "polio, bulbar", "Polio, Bulbar", "Bulbar Poliomyelitis", "Bulbar poliomyelitis", "bulbar poliomyelitis", "Poliomyelitis, Bulbar", "poliomyelitis; bulbar", "bulbar; poliomyelitis", "Acute infantile paralysis", "Acute anterior poliomyelitis", "acute anterior poliomyelitis", "Anterior acute poliomyelitis", "paralytic bulbar poliomyelitis", "Acute bulbar polioencephalitis", "POLIOMYELITIS, ANTERIOR, ACUTE", "POLIOMYELITIS, PARALYTIC, BULBAR", "Anterior acute poliomyelitis, NOS", "Poliomyelitis specified as bulbar", "medullary involvement poliomyelitis", "Medullary Involvement Poliomyelitis", "poliomyelitis, medullary involvement", "Acute paralytic bulbar poliomyelitis", "Poliomyelitis, Medullary Involvement", "Acute paralytic poliomyelitis, bulbar", "Anterior acute poliomyelitis (disorder)", "paralytic bulbar poliomyelitis (diagnosis)", "Acute anterior bulbar polioencephalomyelitis", "Acute paralytic poliomyelitis, bulbar (disorder)", "Acute paralytic poliomyelitis specified as bulbar"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bulbar polio", "shortest_name_length": 12}
{"curie": "MONDO:0001365", "names": ["necrosis of ear ossicle", "partial loss or necrosis of ear ossicles", "Partial loss or necrosis of ear ossicles"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "necrosis of ear ossicle", "shortest_name_length": 23}
{"curie": "UMLS:C0271240", "names": ["Blind eye", "blind eye", "blinding eye", "Blindness;one eye", "one eye blindness", "blindness one eye", "blindness; one eye", "Blindness, one eye", "one eye; blindness", "Unilateral blindness", "Unilateral Blindness", "BLINDNESS UNILATERAL", "Blindness unilateral", "unilateral blindness", "Blindness, Unilateral", "Blindness of one eye, NOS", "Blindness of one eye (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Blindness of one eye (disorder)", "shortest_name_length": 9}
{"curie": "UMLS:C5552101", "names": ["Visual Pathway Tumor", "Tumor of Visual Pathway", "Visual Pathway Neoplasm", "Visual Pathway Neoplasms", "Neoplasm of Visual Pathway", "Tumor of the Visual Pathway", "Neoplasm of the Visual Pathway"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Visual Pathway Neoplasm", "shortest_name_length": 20}
{"curie": "UMLS:C5206756", "names": ["Recurrent Childhood Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Malignant Neoplasm", "shortest_name_length": 38}
{"curie": "MONDO:0001552", "names": ["acalculia", "Acalculia", "Acalculias", "Dyscalculia", "dyscalculia", "Dyscalculias", "Acalculia (finding)", "disorders mathematic", "mathematics disorder", "Mathematics disorder", "Dyscalculia (finding)", "arithmetical disorder", "dyscalculia (disease)", "disorder; arithmetical", "arithmetical; disorder", "math learning disability", "acalculia was demonstrated", "acalculia (physical finding)", "arithmetic learning disability", "disorder of arithmetical skills", "Disorder of arithmetical skills", "Specific arithmetical retardation", "developmental arithmetic disorder", "Developmental arithmetic disorder", "developmental mathematics disorder", "development; arithmetical disorder", "Developmental arithmetical disorder", "arithmetical disorder; developmental", "arithmetical; disorder, developmental", "Basic learning disability, arithmetic", "disorder; arithmetical, developmental", "disturbance; arithmetical, developmental", "Difficulty making arithmetical calculations", "Developmental arithmetic disorder (disorder)", "learning; developmental disorder, arithmetical", "developmental mathematics disorder (diagnosis)", "arithmetic learning disability (physical finding)", "developmental disorder; learning, learning, arithmetical"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyscalculia", "shortest_name_length": 9}
{"curie": "MONDO:0013189", "names": ["TTM", "plucking", "pull hair", "hair pull", "Trichologia", "hair pulling", "pulling hair", "Hair-pulling", "Hair Pulling", "hair-pulling", "Hair plucking", "plucking hair", "hair plucking", "Trichotillomania", "trichotillomania", "TRICHOTILLOMANIA", "Trichotillomanias", "pulling out one's hair", "Trichotillomania (disorder)", "trichotillomania (diagnosis)", "pulling out one's hair (symptom)", "trichotillomania, multifactorial", "Hair pulling, chronic, compulsive, repetitive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichotillomania", "shortest_name_length": 3}
{"curie": "MONDO:0007781", "names": ["EHT", "hypertension, essential", "blood pressure regulation QTL", "genetic essential hypertension", "essential hypertension, genetic", "hypertension, susceptibility to", "hypertension, essential, salt-sensitive", "hypertension, essential, susceptibility to", "hypertension, essential, susceptibility to, 4", "hypertension, essential, susceptibility to, 5", "hypertension, essential, susceptibility to, 6", "hypertension, essential, susceptibility to, 2", "hypertension, essential, susceptibility to, 1", "hypertension, essential, susceptibility to, 3", "hypertension, salt-sensitive essential, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "essential hypertension, genetic", "shortest_name_length": 3}
{"curie": "MONDO:0014844", "names": ["POF12", "PREMATURE OVARIAN FAILURE 12", "premature ovarian failure 12", "SYCE1 primary ovarian failure", "premature ovarian failure type 12", "premature ovarian failure 12; POF12", "primary ovarian failure caused by mutation in SYCE1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "premature ovarian failure 12", "shortest_name_length": 5}
{"curie": "UMLS:C5418988", "names": ["Refractory Hairy Cell Leukemia Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Hairy Cell Leukemia Variant", "shortest_name_length": 38}
{"curie": "UMLS:C1698100", "names": ["intraoperative venous injury", "Intraoperative venous injury", "Intraoperative Venous Injury", "intraoperative venous injury (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraoperative Venous Injury", "shortest_name_length": 28}
{"curie": "MONDO:0006787", "names": ["cystadenoma", "hidrocystoma", "Hidrocystoma", "Hydrocystoma", "Hidrocystomas", "Syringocystoma", "eccrine cystadenoma", "Eccrine cystadenoma", "Eccrine Cystadenoma", "Apocrine cystadenoma", "eccrine hidrocystoma", "apocrine cystadenoma", "Eccrine hidrocystoma", "Eccrine Hidrocystoma", "Apocrine hidrocystoma", "Apocrine Hidrocystoma", "Apocrine hydrocystoma", "Apocrine Hydrocystoma", "Eccrine hidrocystoma of skin", "eccrine hidrocystoma of skin", "apocrine/eccrine hidrocystoma", "Apocrine cystadenoma (disorder)", "hidrocystoma (morphologic abnormality)", "Hidrocystoma (morphologic abnormality)", "Eccrine hidrocystoma of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hidrocystoma", "shortest_name_length": 11}
{"curie": "MONDO:0011752", "names": ["NPHP4", "NEPHRONOPHTHISIS 4", "nephronophthisis 4", "Nephronophthisis 4", "nephronophthisis type 4", "Nephronophthisis type 4", "juvenile nephronophthisis 4", "Nephronophthisis 4, Juvenile", "NEPHRONOPHTHISIS 4, JUVENILE", "nephronophthisis 4, juvenile", "NPHP4 nephronophthisis (disease)", "Nephronophthisis type 4 (disorder)", "nephronophthisis (disease) caused by mutation in NPHP4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephronophthisis 4", "shortest_name_length": 5}
{"curie": "UMLS:C4528619", "names": ["Stage II Vulvar Cancer", "Stage II Vulvar Cancer AJCC v8", "Stage II Vulvar Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Vulvar Cancer AJCC v8", "shortest_name_length": 22}
{"curie": "MONDO:0008787", "names": ["AHMIO1", "microcytic anemia with liver iron overload", "microcytic anemia and hepatic iron overload", "hypochromic microcytic anemia with iron overload", "anemia, hypochromic microcytic, with iron overload 1", "ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 1", "anemia, hypochromic microcytic, with iron overload type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcytic anemia with liver iron overload", "shortest_name_length": 6}
{"curie": "UMLS:C1096213", "names": ["Cannula site reaction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cannula site reaction", "shortest_name_length": 21}
{"curie": "UMLS:C0348893", "names": ["Chronic superficial gastritis", "gastritis chronic superficial", "gastritis; superficial chronic", "superficial; gastritis, chronic", "gastritis; chronic, superficial", "chronic; gastritis, superficial", "Persistent Superficial Gastritis", "CSG - Chronic superficial gastritis", "Chronic superficial gastritis (disorder)", "Chronic superficial gastritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic superficial gastritis", "shortest_name_length": 29}
{"curie": "UMLS:C1378109", "names": ["Pharyngeal Cancer Stage III", "Stage III Pharynx Carcinoma", "Stage III Pharyngeal Cancer", "Stage III Carcinoma of Pharynx", "Stage III Pharyngeal Carcinoma", "Stage III Carcinoma of the Pharynx", "Stage III Pharyngeal Throat Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Pharynx Carcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C0334333", "names": ["Black Adenoma", "Black adenoma", "black; adenoma", "adenoma; black", "Pigmented adenoma", "Pigmented Adrenal Gland Adenoma", "Pigmented Adrenal Cortex Adenoma", "Pigmented Adrenal Cortical Adenoma", "Adrenal cortical adenoma, pigmented", "Heavily Pigmented Adrenocortical Adenoma", "Heavily Pigmented Adrenal Cortex Adenoma", "Heavily Pigmented Adrenal Cortical Adenoma", "Adrenal cortical adenoma, heavily pigmented variant", "Adrenal cortical adenoma - heavily pigmented variant", "Adrenal cortical adenoma, pigmented (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Heavily Pigmented Adrenal Cortical Adenoma", "shortest_name_length": 13}
{"curie": "UMLS:C0553548", "names": ["necrotizing angitis", "necrotizing angiitis", "Angiitis necrotizing", "Necrotising angiitis", "Angiitis necrotising", "necrotising angiitis", "ANGIITIS NECROTIZING", "Necrotizing angiitis", "necrotizing; angiitis", "angiitis; necrotizing", "Necrotising arteritis", "Necrotizing Arteritis", "ANGIITIS, NECROTIZING", "necrotizing arteritis", "Necrotizing arteritis", "necrotizing; arteritis", "arteritis; necrotizing", "Arteritis, Necrotizing", "Necrotizing Arteritides", "Arteritides, Necrotizing", "Necrotizing arteritis (disorder)", "necrotizing angiitis (diagnosis)", "disseminated necrotizing periarteritis", "Disseminated necrotizing periarteritis", "disseminated necrotizing periarteritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Necrotizing Arteritis", "shortest_name_length": 19}
{"curie": "MONDO:0016143", "names": ["gamma-sarcoglycanopathy", "qualitative or quantitative defects of gamma-sarcoglycan"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of gamma-sarcoglycan", "shortest_name_length": 23}
{"curie": "MONDO:0016817", "names": ["Meier-Gorlin syndrome", "ear-patella-short stature syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meier-Gorlin syndrome", "shortest_name_length": 21}
{"curie": "UMLS:C1708767", "names": ["Lung Biphasic Synovial Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Biphasic Synovial Sarcoma", "shortest_name_length": 30}
{"curie": "MONDO:0011077", "names": ["Microcephaly, facial clefting, and preaxial polydactyly", "microcephaly, facial clefting, and preaxial polydactyly", "microcephaly, corpus callosum dysgenesis and cleft lip-palate", "Microcephaly, corpus callosum dysgenesis and cleft lip-palate", "MICROCEPHALY, CORPUS CALLOSUM DYSGENESIS, AND CLEFT LIP/PALATE", "Microcephaly, Corpus Callosum Dysgenesis, And Cleft Lip-Palate", "microcephaly, corpus callosum dysgenesis, and cleft lip/palate", "corpus callosum dysgenesis, microcephaly, infantile spasm, cleft lip-palate, exophthalmos and psychomotor retardation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly, corpus callosum dysgenesis, and cleft lip/palate", "shortest_name_length": 55}
{"curie": "UMLS:C4526980", "names": ["Stage IIIB Small Intestinal, Esophageal, Colorectal, Mesenteric, and Peritoneal GIST AJCC v8", "Stage IIIB Small Intestinal, Esophageal, Colorectal, Mesenteric, and Peritoneal Gastrointestinal Stromal Tumor (GIST)", "Stage IIIB Small Intestinal, Esophageal, Colorectal, Mesenteric, and Peritoneal Gastrointestinal Stromal Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Small Intestinal, Esophageal, Colorectal, Mesenteric, and Peritoneal Gastrointestinal Stromal Tumor AJCC v8", "shortest_name_length": 92}
{"curie": "MONDO:0022613", "names": ["bruyn scheltens syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bruyn scheltens syndrome", "shortest_name_length": 24}
{"curie": "MONDO:0015182", "names": ["congenital enteropathy involving intestinal mucosa development"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital enteropathy involving intestinal mucosa development", "shortest_name_length": 62}
{"curie": "UMLS:C0259797", "names": ["Dog Bite", "Dog bite", "bite dog", "dog bite", "Bite;dog", "bites dog", "Dog bites", "Dog Bites", "bites dogs", "Bitten by dog", "Dog bite (event)", "dog bite (diagnosis)", "injury caused by dog bite"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dog Bite", "shortest_name_length": 8}
{"curie": "MONDO:0006892", "names": ["Sensory Partial Epilepsy", "partial sensory epilepsy", "Sensory Seizure Disorder", "Partial Epilepsy, Sensory", "Epilepsy, Sensory Partial", "Sensory Seizure Disorders", "Seizure Disorder, Sensory", "Epilepsy, Partial, Sensory", "Seizure Disorders, Sensory", "Sensory Focal Seizure Disorder", "Focal Seizure Disorder, Sensory", "Sensory Partial Seizure Disorder", "Seizure Disorder, Sensory, Focal", "Seizure Disorder, Partial, Sensory"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial sensory epilepsy", "shortest_name_length": 24}
{"curie": "MONDO:0020153", "names": ["Cryptophthalmia", "cryptophthalmia", "CRYPTOPHTHALMIA", "Cryptophthalmos", "cryptophthalmos", "Cryptophthalmos NOS", "Globe of eye vestigial", "congenital cryptophthalmos", "Cryptophthalmos (disorder)", "congenital cryptophthalmos (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cryptophthalmia", "shortest_name_length": 15}
{"curie": "MONDO:0014244", "names": ["HSAN7", "HSAN 7", "HSAN VII", "hereditary sensory and autonomic neuropathy type 7", "Hereditary sensory and autonomic neuropathy type 7", "Hereditary sensory and autonomic neuropathy type VII", "neuropathy, hereditary sensory and autonomic, type 7", "Hereditary Sensory and Autonomic Neuropathy Type VII", "hereditary sensory and autonomic neuropathy type VII", "NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII", "Neuropathy, Hereditary Sensory and Autonomic, Type VII", "neuropathy, hereditary sensory and autonomic, type VII", "CIP with hyperhidrosis and gastrointestinal dysfunction", "HSAN with hyperhidrosis and gastrointestinal dysfunction", "HSAN7- hereditary sensory and autonomic neuropathy type 7", "Hereditary sensory and autonomic neuropathy type 7 (disorder)", "SCN11A autosomal dominant hereditary sensory and autonomic neuropathy", "Congenital insensitivity to pain with hyperhidrosis and gastrointestinal dysfunction", "congenital insensitivity to pain with hyperhidrosis and gastrointestinal dysfunction", "INSENSITIVITY TO PAIN, CONGENITAL, WITH GASTROINTESTINAL DYSFUNCTION AND HYPERHIDROSIS", "insensitivity to pain, congenital, with gastrointestinal dysfunction and hyperhidrosis", "autosomal dominant hereditary sensory and autonomic neuropathy caused by mutation in SCN11A", "hereditary sensory and autonomic neuropathy with hyperhidrosis and gastrointestinal dysfunction", "Hereditary sensory and autonomic neuropathy with hyperhidrosis and gastrointestinal dysfunction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary sensory and autonomic neuropathy type 7", "shortest_name_length": 5}
{"curie": "MONDO:0011344", "names": ["parotitis, juvenile recurrent", "PAROTITIS, JUVENILE RECURRENT", "Parotitis, Juvenile Recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parotitis, juvenile recurrent", "shortest_name_length": 29}
{"curie": "MONDO:0021520", "names": ["Benign Floor of Mouth Tumor", "mouth floor benign neoplasm", "benign floor of mouth tumor", "benign tumor of floor of mouth", "Benign Tumor of Floor of Mouth", "Benign tumor of floor of mouth", "benign floor of mouth neoplasm", "Benign Floor of Mouth Neoplasm", "Benign tumour of floor of mouth", "Benign Floor of the Mouth Tumor", "benign floor of the mouth tumor", "benign neoplasm of floor of mouth", "Benign Neoplasm of Floor of Mouth", "Benign neoplasm of floor of mouth", "Benign Floor of the Mouth Neoplasm", "benign floor of the mouth neoplasm", "FOM - Benign tumor of floor of mouth", "FOM - Benign tumour of floor of mouth", "Benign Tumor of the Floor of the Mouth", "Benign neoplasm of floor of mouth, NOS", "benign tumor of the floor of the mouth", "benign neoplasm of the floor of the mouth", "Benign Neoplasm of the Floor of the Mouth", "Benign neoplasm of floor of mouth (disorder)", "benign neoplasm of floor of mouth (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of floor of mouth", "shortest_name_length": 27}
{"curie": "MONDO:0004010", "names": ["infiltrating ureter transitional cell carcinoma", "infiltrating renal pelvis/ureter urothelial carcinoma", "Upper Urinary Tract Infiltrating Urothelial Carcinoma", "infiltrating renal pelvis and ureter urothelial carcinoma", "Infiltrating Renal Pelvis and Ureter Urothelial Carcinoma", "Infiltrating Renal Pelvis and Ureter Transitional Cell Carcinoma", "infiltrating renal pelvis and ureter transitional cell carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infiltrating renal pelvis/ureter urothelial carcinoma", "shortest_name_length": 47}
{"curie": "UMLS:C4324396", "names": ["Immune-mediated hepatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immune-mediated hepatitis", "shortest_name_length": 25}
{"curie": "MONDO:0011031", "names": ["DFNA10", "autosomal dominant deafness 10", "deafness, autosomal dominant 10", "Deafness, Autosomal Dominant 10", "DEAFNESS, AUTOSOMAL DOMINANT 10", "deafness, autosomal dominant type 10", "autosomal dominant nonsyndromic deafness 10", "EYA4 autosomal dominant nonsyndromic deafness", "autosomal dominant nonsyndromic hearing loss 10", "autosomal dominant nonsyndromic deafness type 10", "autosomal dominant nonsyndromic deafness caused by mutation in EYA4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 10", "shortest_name_length": 6}
{"curie": "UMLS:C1095923", "names": ["Febrile bone marrow aplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Febrile bone marrow aplasia", "shortest_name_length": 27}
{"curie": "MONDO:0007512", "names": ["Ectodermal Dysplasia Syndrome with Distinctive Facial Appearance and Preaxial Polydactyly of Feet", "ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE AND PREAXIAL POLYDACTYLY OF FEET", "ectodermal dysplasia syndrome with distinctive facial appearance and preaxial polydactyly of feet"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia syndrome with distinctive facial appearance and preaxial polydactyly of feet", "shortest_name_length": 97}
{"curie": "MONDO:0027675", "names": ["irinotecan toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "irinotecan toxicity", "shortest_name_length": 19}
{"curie": "UMLS:C5419748", "names": ["Skin Epithelioid Malignant Peripheral Nerve Sheath Tumor", "Dermal Epithelioid Malignant Peripheral Nerve Sheath Tumor", "Cutaneous Epithelioid Malignant Peripheral Nerve Sheath Tumor", "Epithelioid Malignant Peripheral Nerve Sheath Tumor of the Skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epithelioid Malignant Peripheral Nerve Sheath Tumor of the Skin", "shortest_name_length": 56}
{"curie": "UMLS:C5421309", "names": ["Refractory Ovarian Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Ovarian Adenocarcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0009519", "names": ["LESD", "L-S DISEASE", "L-S disease", "Letterer-Siwe", "histiocytosis x", "Histiocytosis X", "HISTIOCYTOSIS X I", "Histiocytosis X NOS", "letterer siwe disease", "Letterer-Siwe Disease", "Acute histiocytosis X", "letterer-Siwe disease", "letterer-siwe disease", "LETTERER-SIWE DISEASE", "Letterer Siwe disease", "Letterer-Siwe disease", "Letterer-Siwe's disease", "letterer - siwe disease", "ABT-LETTERER-SIWE DISEASE", "Acute infancy reticulosis", "LSD - Letterer-Siwe disease", "Acute reticulosis of infancy", "Nonlipid reticuloendotheliosis", "Familial Letterer-Siwe disease", "Langerhans cell granulomatosis", "nonlipid; reticuloendotheliosis", "reticuloendotheliosis; nonlipid", "Non-lipid reticuloendotheliosis", "Letterer-Siwe disease (clinical)", "Acute progressive histiocytosis X", "Letterer-Siwe disease (diagnosis)", "histiocytosis X, acute disseminated", "Histiocytosis X, acute disseminated", "HISTIOCYTOSIS X, ACUTE DISSEMINATED", "X; histiocytosis, acute (progressive)", "Acute infantile reticuloendotheliosis", "histiocytosis; X, acute (progressive)", "reticuloendotheliosis; acute infantile", "RETICULOENDOTHELIOSIS, SYSTEMIC ALEUKEMIC", "Langerhans cell histiocytosis, generalised", "Langerhans cell histiocytosis, generalized", "Langerhans cell histiocytosis, disseminated", "acute; reticuloendotheliosis, acute infantile", "Acute differentiated progressive histiocytosis", "histiocytosis; acute differentiated progressive", "Acute Disseminated Langerhans Cell Histiocytosis", "acute; differentiated progressive, histiocytosis", "acute disseminated Langerhans cell histiocytosis", "acute and disseminated Langerhans cell histiocytosis", "multifocal multisystem Langerhans cell histiocytosis", "Multifocal Multisystem Langerhans Cell Histiocytosis", "Langerhans cell histiocytosis, disseminated (clinical)", "Langerhans cell histiocytosis, disseminated (disorder)", "Langerhans cell histiocytosis, disseminated (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "letterer-Siwe disease", "shortest_name_length": 4}
{"curie": "MONDO:0001251", "names": ["Chronic apical periodontitis", "chronic apical periodontitis", "chronic periodontitis apical", "chronic periapical periodontitis", "Chronic periapical periodontitis", "periapical periodontitis, chronic", "CAP - chronic apical periodontitis", "Chronic periradicular periodontitis", "Asymptomatic periapical periodontitis", "chronic apical periodontitis (diagnosis)", "Asymptomatic periapical periodontitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic apical periodontitis", "shortest_name_length": 28}
{"curie": "MONDO:0013491", "names": ["MLC2B", "megalencephalic leukoencephalopathy with subcortical cysts 2B", "megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without mental retardation", "megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without intellectual disability", "MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2B, REMITTING, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT", "MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2B, REMITTING, WITH OR WITHOUT INTELLECTUAL DEVELOPMENTAL DISORDER"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without intellectual disability", "shortest_name_length": 5}
{"curie": "MONDO:0009837", "names": ["CPP", "choroid plexus carcinoma", "Choroid Plexus Papilloma", "choroid plexus papilloma", "CHOROID PLEXUS PAPILLOMA", "Choroid plexus papilloma", "Choroid Plexus Papillomas", "CHOROID PLEXUS, PAPILLOMA", "Papilloma, Choroid Plexus", "choroid plexus; papilloma", "choroid plexus papillomas", "papilloma; choroid plexus", "Papillomas, Choroid Plexus", "Papilloma of choroid plexus", "PAPILLOMA OF CHOROID PLEXUS", "papilloma of choroid plexus", "Papilloma of Choroid Plexus", "plexus choroideus; papilloma", "Choroid plexus papilloma NOS", "Choroid plexus papilloma, NOS", "Benign choroid plexus papilloma", "papilloma of the choroid plexus", "Papilloma of the Choroid Plexus", "papilloma, choroid plexus, benign", "PAPILLOMA, CHOROID PLEXUS, BENIGN", "childhood choroid plexus papilloma", "Pediatric Choroid Plexus Papilloma", "Benign papilloma of choroid plexus", "Childhood Choroid Plexus Papilloma", "childhood papilloma of choroid plexus", "pediatric papilloma of choroid plexus", "BRAIN TUMOR, CHOROID PLEXUS PAPILLOMA", "Childhood Papilloma of Choroid Plexus", "Pediatric Papilloma of Choroid Plexus", "papilloma of choroid plexus (diagnosis)", "Childhood Papilloma of the Choroid Plexus", "Pediatric Papilloma of the Choroid Plexus", "choroid plexus papilloma, no ICD-O subtype", "Benign papilloma of choroid plexus (disorder)", "INTRACRANIAL NEOPLASM, CHOROID PLEXUS PAPILLOMA", "choroid plexus papilloma NOS (morphologic abnormality)", "Benign choroid plexus papilloma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choroid plexus papilloma", "shortest_name_length": 3}
{"curie": "UMLS:C1320453", "names": ["CIN 3", "Cervix Squamous Cell Carcinoma In Situ", "Severe Squamous Dysplasia of the Cervix", "Cervical Squamous Cell Carcinoma In Situ", "squamous cell carcinoma in situ of cervix", "Squamous Cell Carcinoma In Situ of Cervix", "Cervix Uteri Squamous Cell Carcinoma In Situ", "cervical squamous intraepithelial neoplasia 3", "Squamous Cell Carcinoma In Situ of the Cervix", "Cervical Squamous Intraepithelial Neoplasia 3", "Uterine Cervix Squamous Cell Carcinoma In Situ", "Squamous Cell Carcinoma In Situ of Cervix Uteri", "Cervical Squamous Cell Carcinoma In Situ AJCC v7", "Squamous cell carcinoma in situ of uterine cervix", "Squamous Cell Carcinoma In Situ of Uterine Cervix", "Squamous Cell Carcinoma In Situ of the Cervix Uteri", "squamous cell carcinoma in situ of cervix (diagnosis)", "Squamous Cell Carcinoma In Situ of the Uterine Cervix", "grade III squamous intraepithelial neoplasia of cervix", "Squamous cell carcinoma in situ of uterine cervix (disorder)", "grade III squamous intraepithelial neoplasia of cervix (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Squamous Cell Carcinoma In Situ", "shortest_name_length": 5}
{"curie": "UMLS:C3272520", "names": ["Small Intestinal B-Cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Intestinal B-Cell Non-Hodgkin Lymphoma", "shortest_name_length": 44}
{"curie": "MONDO:0002749", "names": ["extracranial neuroblastoma", "Extracranial Neuroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extracranial neuroblastoma", "shortest_name_length": 26}
{"curie": "UMLS:C0334249", "names": ["Epidermoid carcinoma, small cell, nonkeratinising", "Epidermoid carcinoma, small cell, nonkeratinizing", "Non-keratinizing epidermoid carcinoma - small cell", "nonkeratinizing small cell squamous cell carcinoma", "Non-keratinising epidermoid carcinoma - small cell", "small cell, nonkeratinizing squamous cell carcinoma", "Non-Keratinizing Small Cell Squamous Cell Carcinoma", "Squamous cell carcinoma, small cell, nonkeratinising", "Squamous cell carcinoma, small cell, nonkeratinizing", "Non-keratinising squamous cell carcinoma - small cell", "Non-keratinizing squamous cell carcinoma - small cell", "Epidermoid carcinoma, small cell, non-keratinizing type", "Squamous cell carcinoma, small cell, non-keratinizing type", "nonkeratinizing small cell squamous cell carcinoma (diagnosis)", "Squamous cell carcinoma, small cell, nonkeratinizing (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Squamous cell carcinoma, small cell, nonkeratinizing", "shortest_name_length": 49}
{"curie": "UMLS:C0279525", "names": ["CLNHL", "Lymphoblastic Lymphoma", "NHL, childhood lymphoblastic", "pediatric lymphoblastic lymphoma", "Childhood Lymphoblastic Lymphoma", "childhood lymphoblastic lymphoma", "Pediatric Lymphoblastic Lymphoma", "lymphoblastic lymphoma, pediatric", "lymphoma, pediatric lymphoblastic", "lymphoma, childhood lymphoblastic", "lymphoblastic lymphoma, childhood", "Childhood Precursor Lymphoblastic Lymphoma", "pediatric lymphoblastic non-Hodgkin's lymphoma", "lymphoblastic non-Hodgkin's lymphoma, childhood", "non-Hodgkin's lymphoma, childhood lymphoblastic", "lymphoma, childhood lymphoblastic non-Hodgkin's"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Lymphoblastic Lymphoma", "shortest_name_length": 5}
{"curie": "MONDO:0004651", "names": ["VARIOLA", "Variola", "variola", "SMALLPOX", "Variolas", "Smallpox", "smallpox", "Small pox", "small pox", "Variola, NOS", "variola major", "Smallpox, NOS", "smallpox disease", "ordinary smallpox", "Ordinary smallpox", "smallpox (variola)", "Classical smallpox", "Smallpox (disorder)", "smallpox (diagnosis)", "Smallpox, unspecified", "variola virus infection", "smallpox virus infection", "variola virus VAR infection", "Variola virus infectious disease", "Variola virus disease or disorder", "Variola virus caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "smallpox", "shortest_name_length": 7}
{"curie": "MONDO:0015384", "names": ["enteric duplication cyst of the tongue", "foregut duplication cyst of the tongue", "gastric duplication cyst of the tongue", "digestive duplication cyst of the tongue", "tongue cysts and fistulae of the face and oral cavity", "cysts and fistulae of the face and oral cavity of tongue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "digestive duplication cyst of the tongue", "shortest_name_length": 38}
{"curie": "UMLS:C4553747", "names": ["Stage IV Adrenal Cortex Cancer", "stage IV adrenocortical cancer", "stage IV adrenocortical carcinoma", "stage IV adrenal cortex carcinoma", "carcinoma, adrenocortical stage IV", "adrenocortical carcinoma, stage IV", "metastatic adrenocortical carcinoma", "carcinoma, adrenocortical metastatic", "adrenocortical carcinoma, metastatic", "Stage IV Adrenal Cortex Carcinoma AJCC v8", "stage IV adrenal cortex carcinoma AJCC v8", "Stage IV Adrenal Cortical Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Adrenal Cortex Carcinoma AJCC v8", "shortest_name_length": 30}
{"curie": "UMLS:C5420037", "names": ["Benign Sinonasal Neoplasm", "Benign Nasal Cavity and Paranasal Sinus Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Sinonasal Neoplasm", "shortest_name_length": 25}
{"curie": "MONDO:0011220", "names": ["PARK3", "Parkinson disease 3", "Parkinson's disease 3", "Parkinson disease type 3", "autosomal dominant Parkinson disease", "autosomal dominant Parkinson disease 3", "parkinson disease 3, autosomal dominant", "Parkinson disease 3, autosomal dominant", "PARKINSON DISEASE 3, AUTOSOMAL DOMINANT", "Parkinson Disease 3, Autosomal Dominant", "autosomal dominant Lewy body Parkinson disease 3", "Parkinson disease 3, autosomal dominant Lewy body", "PARKINSON DISEASE 3, AUTOSOMAL DOMINANT LEWY BODY", "Parkinson Disease 3, Autosomal Dominant Lewy Body", "PARKINSON DISEASE 3, AUTOSOMAL DOMINANT LEWY BODY (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parkinson disease 3, autosomal dominant", "shortest_name_length": 5}
{"curie": "UMLS:C4683633", "names": ["Lymphocyte-Depleted Classic Hodgkin Lymphoma by Ann Arbor Stage", "Lymphocyte-Depleted Classical Hodgkin Lymphoma by Ann Arbor Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphocyte-Depleted Classic Hodgkin Lymphoma by Ann Arbor Stage", "shortest_name_length": 63}
{"curie": "MONDO:0020672", "names": ["vascular occlusion", "vascular occlusion disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vascular occlusion disorder", "shortest_name_length": 18}
{"curie": "UMLS:C4289812", "names": ["Cervical Microglandular Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Microglandular Hyperplasia", "shortest_name_length": 35}
{"curie": "MONDO:0005925", "names": ["Shipping Fever", "Shipping fever", "Transport fever", "Fever, Shipping", "Pneumonic pasteurellosis", "pneumonic pasteurellosis", "Pneumonic Pasteurellosis", "Pasteurellosis, Pneumonic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pneumonic pasteurellosis", "shortest_name_length": 14}
{"curie": "UMLS:C0279600", "names": ["TdT negative childhood ALL", "childhood ALL, TdT negative", "ALL, pediatric TdT negative", "pediatric ALL, TdT negative", "ALL, childhood TdT negative", "TdT negative ALL, childhood", "ALL, TdT negative, childhood", "ALL, TdT negative, pediatric", "TdT Negative Acute Lymphoblastic Leukemia", "TdT negative childhood acute lymphocytic leukemia", "TdT negative pediatric acute lymphocytic leukemia", "leukemia, pediatric acute lymphocytic TdT negative", "leukemia, childhood acute lymphocytic TdT negative", "acute lymphocytic leukemia, childhood TdT negative", "TdT negative lymphocytic leukemia, acute childhood", "TdT negative acute lymphocytic leukemia, childhood", "Childhood TdT Negative Acute Lymphoblastic Leukemia", "TdT negative childhood acute lymphoblastic leukemia", "acute lymphoblastic leukemia, childhood TdT negative"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood TdT Negative Acute Lymphoblastic Leukemia", "shortest_name_length": 26}
{"curie": "UMLS:C4330969", "names": ["Stage I HPV-Mediated (p16-Positive) Oropharyngeal Throat Cancer", "Pathologic Stage I HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage I HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8", "shortest_name_length": 63}
{"curie": "UMLS:C0086196", "names": ["Infantile Eczema", "eczema infantile", "ECZEMA INFANTILE", "Infantile eczema", "infantile eczema", "Eczema;infantile", "Eczema infantile", "Eczema, Infantile", "eczema; infantile", "infantile; eczema", "Infantile eczema (disorder)", "infantile eczema (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eczema, Infantile", "shortest_name_length": 16}
{"curie": "MONDO:0010146", "names": ["kerion", "Kerion", "kerion celsi", "Kerion Celsi", "Kerion celsi", "tinea kerion", "Tinea kerion", "tinea; kerion", "kerion; tinea", "Suppurative ringworm", "Tinea capitis profunda", "Trichophyton infection", "Tinea kerion (disorder)", "tinea kerion (diagnosis)", "Suppurative dermatophytosis", "trichophytia profunda barbae", "trichophytia profunda capitis", "susceptibility to Tinea imbricata", "TINEA IMBRICATA, SUSCEPTIBILITY TO", "TINEA imbricata, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kerion celsi", "shortest_name_length": 6}
{"curie": "UMLS:C0019285", "names": ["Traumatic diaphragmatic hernia", "Traumatic Diaphragmatic Hernia", "traumatic diaphragmatic hernia", "diaphragmatic hernia traumatic", "Hernia, Traumatic Diaphragmatic", "Traumatic Diaphragmatic Hernias", "Diaphragmatic Hernia, Traumatic", "Diaphragmatic Hernias, Traumatic", "Hernias, Traumatic Diaphragmatic", "Hernia, Diaphragmatic, Traumatic", "Traumatic diaphragmatic hernia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hernia, Diaphragmatic, Traumatic", "shortest_name_length": 30}
{"curie": "MONDO:0009661", "names": ["MPS6", "MPSVI", "MPS 6", "MPS VI", "ASB deficiency", "Maroteaux-Lamy", "Arsb deficiency", "ARSB deficiency", "ARSB Deficiency", "ARSB DEFICIENCY", "Deficiency, ARSB", "ARSB Deficiencies", "Deficiencies, ARSB", "Maroteaux-Lamy disease", "Mucopolysaccharidosis 6", "Maroteaux Lamy Syndrome", "Maroteaux Lamy syndrome", "Maroteaux-Lamy syndrome", "Maroteaux-Lamy Syndrome", "MAROTEAUX-LAMY SYNDROME", "Polydystrophic dwarfism", "polydystrophic dwarfism", "Polydystrophic Dwarfism", "DWARFISM, POLYDYSTROPHIC", "mucopolysaccharidosis VI", "MUCOPOLYSACCHARIDOSIS VI", "Mucopolysaccharidosis VI", "Syndrome, Maroteaux-Lamy", "Dwarfism, Polydystrophic", "Maroteaux-Lamy syndrome I", "Maroteaux - Lamy syndrome", "arylsulfatase B deficiency", "Arylsulfatase B deficiency", "Arylsulfatase B Deficiency", "ARYLSULFATASE B DEFICIENCY", "Deficiency, Arylsulfatase B", "Arylsulphatase B deficiency", "Mucopolysaccharidosis type 6", "Mucopolysaccharidosis Type 6", "Maroteaux-Lamy syndrome, NOS", "Arylsulfatase B Deficiencies", "mucopolysaccharidosis type 6", "mucopolysaccharidosis type VI", "Deficiencies, Arylsulfatase B", "Type 6, Mucopolysaccharidosis", "Mucopolysaccharidosis Type VI", "Mucopolysaccharidosis type VI", "Mucopolysaccharidosis, MPS-VI", "Mucopoly-saccharidosis type VI", "mucopolysaccharidosis (MPS) VI", "MUCOPOLYSACCHARIDOSIS, TYPE VI", "type VI; mucopolysaccharidosis", "Type VI, Mucopolysaccharidosis", "MPS VI - Maroteaux-Lamy syndrome", "arylsulfatase B (ARSB) deficiency", "ARSB - Arylsulfatase B deficiency", "MPS VI - Mucopolysaccharidosis VI", "ARSB - Arylsulphatase B deficiency", "Maroteaux-Lamy syndrome (disorder)", "Maroteaux-Lamy syndrome (diagnosis)", "mucopolysaccharide storage disease VI", "Mucopolysaccharidosis, type VI (MPS VI)", "Mucopolysaccharidosis chondroitin sulfate B", "Mucopolysaccharidosis chondroitin sulphate B", "N-acetylgalactosamine-4-sulfatase deficiency", "N-acetylgalactosamine 4-sulfatase deficiency", "N-ACETYLGALACTOSAMINE-4-SULFATASE DEFICIENCY", "N-Acetylgalactosamine-4-Sulfatase Deficiency", "N-Acetylgalactosamine-4-sulfatase deficiency", "N-acetylgalactosamine-4-sulphatase deficiency", "N-Acetylgalactosamine-4-sulphatase deficiency", "Deficiency, N-Acetylgalactosamine-4-Sulfatase", "N-Acetylgalactosamine-4-Sulfatase Deficiencies", "mucopolysaccharidosis type VI (Maroteaux-Lamy)", "Deficiency of N-acetylgalactosamine-4-sulfatase", "deficiency of N-acetylgalactosamine-4-sulfatase", "Deficiencies, N-Acetylgalactosamine-4-Sulfatase", "Deficiency of N-acetylgalactosamine-4-sulphatase", "Deficiency of N-acetylgalactosamine-4-sulfatase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucopolysaccharidosis type 6", "shortest_name_length": 4}
{"curie": "MONDO:0001719", "names": ["bursitis gonococcal", "Gonococcal bursitis", "gonococcal bursitis", "Neisseria gonorrhoeae bursitis", "Gonococcal bursitis (diagnosis)", "Neisseria gonorrhoeae caused bursitis", "Gonococcal bursitis, site unspecified", "Bursitis caused by Neisseria gonorrhoeae", "Bursitis caused by Neisseria gonorrhoeae (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gonococcal bursitis", "shortest_name_length": 19}
{"curie": "UMLS:C0279834", "names": ["oropharynx cancer, stage I", "stage I oropharyngeal cancer", "Stage I Oropharynx Carcinoma", "Stage I Oropharyngeal Cancer", "Oropharyngeal cancer stage I", "oropharyngeal cancer, stage I", "Oropharyngeal Cancer, Stage I", "Stage I Oropharyngeal Carcinoma", "Stage I Carcinoma of Oropharynx", "Stage I Oropharyngeal Throat Cancer", "Stage I Carcinoma of the Oropharynx", "Stage I Oropharyngeal Carcinoma AJCC v6", "Stage I Oropharyngeal Carcinoma AJCC v7", "Stage I Oropharyngeal Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Oropharyngeal Carcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0011391", "names": ["VL", "LVM", "MLC", "MLC1", "Van der Knapp disease", "VAN DER KNAAP DISEASE", "Van Der Knapp Disease", "Van der Knaap syndrome", "megalencephalic leukodystrophy", "Megalencephalic leukodystrophy", "Vacuolating leukoencephalopathy", "Vacuolating Leukoencephalopathy", "Vacuolating leucoencephalopathy", "megalencephaly-cystic leukodystrophy", "Megalencephaly-cystic leukodystrophy", "Leucoencephalopathy with swelling and cysts", "Leukoencephalopathy with swelling and cysts", "LEUKOENCEPHALOPATHY WITH SWELLING AND CYSTS", "Megalencephaly-cystic leukodystrophy syndrome", "megalencephaly-cystic leukodystrophy syndrome", "Infantile leucoencephalopathy and megalencephaly", "Infantile leukoencephalopathy and megalencephaly", "Infantile Leukoencephalopathy and Megalencephaly", "megalencephalic leukoencephalopathy with subcortical cysts", "Megalencephalic leucoencephalopathy with subcortical cysts", "Megalencephalic leukoencephalopathy with subcortical cysts", "MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS", "megalencephalic leukoencephalopathy with subcortical cysts 1", "MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 1", "Leukoencephalopathy with Swelling and A Discrepantly Mild Course", "megalencephalic leukoencephalopathy with subcortical cysts type 1", "Megalencephalic leukoencephalopathy with subcortical cysts (disorder)", "Vacuolating megalencephalic leucoencephalopathy with subcortical cysts", "vacuolating megalencephalic leukoencephalopathy with subcortical cysts", "VACUOLATING MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS", "Vacuolating megalencephalic leukoencephalopathy with subcortical cysts", "megalencephalic leukodystrophy megalencephaly-cystic leukodystorphy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "megalencephalic leukoencephalopathy with subcortical cysts", "shortest_name_length": 2}
{"curie": "UMLS:C0702266", "names": ["BASOPHILIA", "Basophilia", "basophilia", "basophilia disorder", "basophilia test result", "basophilia (diagnosis)", "Basophilic leukocytosis", "basophilic leukocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Basophilia", "shortest_name_length": 10}
{"curie": "UMLS:C1261562", "names": ["Unstable bladder", "unstable bladder", "Irritable bladder", "irritable bladder", "bladder irritable", "irritation bladder", "bladder irritation", "Bladder instability", "bladder instability", "bladder irritability", "Detrusor dyssynergia", "detrusor dyssynergia", "detrusor instability", "Detrusor instability", "DI - detrusor instability", "DI - Detrusor instability", "detrusor bladder instability", "bladder detrusor instability", "Detrusor instability of bladder", "detrusor instability (diagnosis)", "Idiopathic detrusor overactivity", "Idiopathic detrusor overactivity (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Detrusor instability", "shortest_name_length": 16}
{"curie": "MONDO:0015479", "names": ["submucosal cleft palate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "submucosal cleft palate", "shortest_name_length": 23}
{"curie": "MONDO:0044742", "names": ["AREI", "autosomal recessive epidermolytic ichthyosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive epidermolytic ichthyosis", "shortest_name_length": 4}
{"curie": "MONDO:0020159", "names": ["congenital entropion", "Congenital entropion", "Entropion congenital", "congenital; entropion", "entropion; congenital", "entropion; congenital, eyelid", "congenital; entropion, eyelid", "Congenital entropion (disorder)", "congenital entropion (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital entropion", "shortest_name_length": 20}
{"curie": "UMLS:C1336339", "names": ["Stage IVA Liver Cell Carcinoma", "Stage IVA Hepatocellular Cancer", "Stage IVA Hepatocellular Carcinoma", "Stage IVA Hepatocellular Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Hepatocellular Carcinoma AJCC v7", "shortest_name_length": 30}
{"curie": "MONDO:0024662", "names": ["Colorectal Tubulovillous Adenoma", "colorectal tubulovillous adenoma", "Large Bowel Tubulovillous Adenoma", "large bowel tubulovillous adenoma", "tubulovillous adenoma of large bowel", "Tubulovillous Adenoma of Large Bowel", "Tubulovillous Adenoma of the Large Bowel", "tubulovillous adenoma of the large bowel"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorectal tubulovillous adenoma", "shortest_name_length": 32}
{"curie": "MONDO:0003978", "names": ["Oat cell colon carcinoma", "colon Oat cell carcinoma", "Oat Cell Colon Carcinoma", "Colon Oat Cell Carcinoma", "Colon Small Cell Carcinoma", "colonic Oat cell carcinoma", "Small Cell Colon Carcinoma", "colon small cell carcinoma", "small cell colon carcinoma", "Colonic Oat Cell Carcinoma", "Oat Cell Carcinoma of Colon", "Oat cell carcinoma of colon", "Colonic small cell carcinoma", "Colonic Small Cell Carcinoma", "colonic small cell carcinoma", "Small Cell Carcinoma of Colon", "small cell carcinoma of colon", "Oat Cell Carcinoma of the Colon", "Oat cell carcinoma of the colon", "small cell carcinoma of the colon", "Small Cell Carcinoma of the Colon", "colon small cell neuroendocrine cancer", "Colon Small Cell Neuroendocrine Cancer", "Colon Small Cell Neuroendocrine Carcinoma", "colon small cell neuroendocrine carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colon small cell neuroendocrine carcinoma", "shortest_name_length": 24}
{"curie": "MONDO:0002273", "names": ["plasma protein metabolism disease", "Other disorders of plasma protein metabolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "plasma protein metabolism disease", "shortest_name_length": 33}
{"curie": "UMLS:C1518013", "names": ["Low Grade Breast Adenosquamous Carcinoma", "Low Grade Adenosquamous Breast Carcinoma", "Infiltrating Breast Syringomatous Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Grade Breast Adenosquamous Carcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0011569", "names": ["CMT2B1", "CMT 2B1", "AR-CMT2B1", "autosomal recessive axonal CMT4C1", "Autosomal recessive axonal CMT4C1", "Charcot Marie Tooth disease type 2B1", "Charcot-Marie-Tooth disease type 2B1", "Charcot-Marie-Tooth disease, Type 2B1", "Charcot-Marie-Tooth disease, type 2B1", "Charcot-Marie-Tooth neuropathy type 2B1", "LMNA Charcot-Marie-Tooth disease type 2", "Charcot-Marie-Tooth neuropathy, type 2B1", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2B1", "Charcot-Marie-Tooth Neuropathy, Type 2b1", "Charcot-Marie-Tooth disease, axonal, Type 2B1", "Charcot-Marie-Tooth disease neuronal type 2B1", "Charcot-Marie-Tooth disease, axonal, type 2B1", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B1", "Charcot-Marie-Tooth disease type 2B1 (disorder)", "Charcot-Marie-Tooth disease, neuronal, type 2B1", "Charcot-Marie-Tooth disease, neuronal, Type 2B1", "CHARCOT-MARIE-TOOTH DISEASE, NEURONAL, TYPE 2B1", "Charcot-Marie-Tooth disease type 2B1 (diagnosis)", "autosomal recessive Charcot-Marie-Tooth disease type 2B1", "Autosomal recessive Charcot-Marie-Tooth disease type 2B1", "Charcot-Marie-Tooth Disease, Axonal, Autosomal Recessive, B1", "Charcot-Marie-Tooth disease type 2 caused by mutation in LMNA", "Charcot-Marie-Tooth disease, axonal, autosomal recessive, 2B1", "autosomal recessive axonal Charcot-Marie-Tooth disease type 2B1", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2B1", "Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2B1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 2B1", "shortest_name_length": 6}
{"curie": "UMLS:C0162869", "names": ["Aneurysm rupture", "ruptured aneurysm", "Aneurysm;ruptured", "Ruptured Aneurysm", "Aneurysm ruptured", "aneurysm ruptured", "ANEURYSM RUPTURED", "Ruptured aneurysm", "Ruptured Aneurysms", "ruptured aneurysms", "Aneurysm, Ruptured", "Aneurysms, Ruptured", "Ruptured aneurysm, NOS", "Ruptured aneurysm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aneurysm, Ruptured", "shortest_name_length": 16}
{"curie": "MONDO:0005236", "names": ["Xanthoma", "XANTHOMA", "xanthoma", "xanthomas", "Xanthomas", "Xanthomata", "xanthelasma", "XANTHELASMA", "Xanthelasma", "xanthelasmas", "Xanthelasmas", "Xanthoma, NOS", "xanthoma eyelid", "Eyelid Xanthoma", "Xanthoma of eyelid", "xanthoma (disease)", "Xanthoma of Eyelid", "xanthelasma palpebrum", "Xanthelasma Palpebrum", "Xanthelasma of eyelid", "Xanthelasma palpebrum", "Xanthoma of the Eyelid", "Xanthelasma (disorder)", "xanthelasma of eyelids", "Xanthelasma palpebrarum", "Xanthomatous deposition", "xanthelasma palpebrarum", "Xanthomatous Depositions", "eyelid disorder xanthoma", "Deposition, xanthomatous", "Fatty deposits on eyelids", "Benign Eyelid Xanthelasma", "xanthoma (physical finding)", "eyelid disorder xanthelasma", "Xanthomatous deposition, NOS", "Benign Xanthelasma of Eyelid", "Xanthoma of eyelid (disorder)", "Xanthoma of periocular region", "clinical impressions xanthoma", "xanthelasma (physical finding)", "Xanthoma of eyelid (diagnosis)", "Benign Xanthelasma of the Eyelid", "Xanthelasma of periocular region", "Xanthelasma of eyelid (diagnosis)", "Fatty deposits in skin around the eyes", "xanthelasma of eyelids (physical finding)", "Xanthomatous deposition (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "xanthoma", "shortest_name_length": 8}
{"curie": "UMLS:C1707245", "names": ["Campylobacter Jejuni-Associated Small Intestinal Mucosa-Associated Lymphoid Tissue Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Campylobacter Jejuni-Associated Small Intestinal Mucosa-Associated Lymphoid Tissue Lymphoma", "shortest_name_length": 91}
{"curie": "MONDO:0001299", "names": ["diabetic autonomic neuropathy", "Diabetic autonomic neuropathy", "Diabetic Autonomic Neuropathy", "autonomic diabetic neuropathy", "Autonomic Neuropathy, Diabetic", "Neuropathy, Diabetic Autonomic", "Diabetic Autonomic Neuropathies", "Autonomic Neuropathies, Diabetic", "Neuropathies, Diabetic Autonomic", "Autonomic neuropathy due to diabetes", "diabetes mellitus with autonomic neuropathy", "Autonomic neuropathy with diabetes mellitus", "Autonomic neuropathy due to diabetes mellitus", "diabetes mellitus with autonomic neuropathy (diagnosis)", "Autonomic neuropathy due to diabetes mellitus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diabetic autonomic neuropathy", "shortest_name_length": 29}
{"curie": "UMLS:C5551302", "names": ["Broken wrist", "broken wrist", "wrist broken", "broken wrists", "WRIST FRACTURE", "fracture wrist", "Fracture;wrist", "wrist fracture", "Wrist Fracture", "Wrist fracture", "Wrist Fractures", "fractured wrist", "WRIST, FRACTURE", "fractures wrist", "Fractured wrist", "Fracture, Wrist", "fractured wrists", "Fracture of wrist", "fracture of wrist", "Fracture of wrist NOS", "Distal Forearm Fracture", "Fracture, Distal Forearm", "Forearm Fracture, Distal", "Distal Forearm Fractures", "fracture of wrist (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fracture of wrist", "shortest_name_length": 12}
{"curie": "UMLS:C1336437", "names": ["Stage IV Renal Pelvis and Ureter Cancer", "Stage IV Renal Pelvis and Ureter Carcinoma", "Stage IV Renal Pelvis and Ureter Cancer AJCC v7", "Stage IV Renal Pelvis and Ureter Carcinoma AJCC v7", "stage IV transitional cell cancer of the renal pelvis and ureter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Renal Pelvis and Ureter Cancer AJCC v7", "shortest_name_length": 39}
{"curie": "MONDO:0016129", "names": ["EGE", "GI eosinophilia", "eosinophilic enteritis", "Eosinophilic enteritis", "Gastroenteritis eosinophilic", "Eosinophilic gastroenteritis", "Eosinophilic Gastroenteritis", "EOSINOPHILIC GASTROENTERITIS", "gastroenteritis eosinophilic", "eosinophilic gastroenteritis", "Gastrointestinal eosinophilia", "eosinophilic; gastroenteritis", "gastroenteritis; eosinophilic", "Eosinophilic gastroenteropathy", "eosinophilic gastroenterocolitis", "Eosinophilic gastroenterocolitis", "Eosinophilic gastroenteropathy, NOS", "Eosinophilic gastrointestinal disease", "Eosinophilic gastroenteritis (disorder)", "Eosinophilic gastrointestinal disorders", "eosinophilic gastroenteritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eosinophilic gastroenteritis", "shortest_name_length": 3}
{"curie": "MONDO:0018660", "names": ["hemophilia", "Hemophilia", "HEMOPHILIA", "Haemophilia", "haemophilia", "hemophilias", "Hemophiliac", "Hemophilia NOS", "Hemophilia, NOS", "Haemophilia NOS", "Haemophilia, NOS", "hemophilia disorder", "Hemophilia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemophilia", "shortest_name_length": 10}
{"curie": "MONDO:0003819", "names": ["childhood ovarian teratoma", "Pediatric Ovarian Teratoma", "pediatric ovarian teratoma", "Childhood Ovarian Teratoma", "pediatric teratoma of Ovary", "pediatric teratoma of ovary", "Pediatric Teratoma of Ovary", "Childhood Teratoma of Ovary", "childhood teratoma of ovary", "ovarian teratoma of childhood", "Childhood Teratoma of the Ovary", "pediatric teratoma of the ovary", "Pediatric Teratoma of the Ovary", "childhood teratoma of the ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood teratoma of the ovary", "shortest_name_length": 26}
{"curie": "UMLS:C5419019", "names": ["Ann Arbor Stage IIX (Bulky) Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage IIX (Bulky) Diffuse Large B-Cell Lymphoma", "shortest_name_length": 57}
{"curie": "UMLS:C0751280", "names": ["Cystic Periventricular Leukomalacia", "Leukomalacia, Cystic Periventricular", "Cystic Periventricular Leukomalacias", "Periventricular Leukomalacia, Cystic", "Periventricular Leukomalacias, Cystic", "Leukomalacias, Cystic Periventricular"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cystic Periventricular Leukomalacia", "shortest_name_length": 35}
{"curie": "MONDO:0010870", "names": ["Tmd", "TMD", "UDD MYOPATHY", "Udd Myopathy", "Udd myopathy", "Myopathy, Udd", "Distal titinopathy", "distal titinopathy", "Udd distal myopathy", "Udd Distal Myopathy", "Myopathy, Udd Distal", "Distal Myopathy, Udd", "Udd type distal myopathy", "Tibial muscular dystrophy", "distal myopathy, Udd type", "Distal myopathy, Udd type", "tibial muscular dystrophy", "Tibial Muscular Dystrophy", "Muscular Dystrophy, Tibial", "Muscular Dystrophies, Tibial", "Finnish tibial muscular dystrophy", "Udd-Markesbery muscular dystrophy", "TARDIVE TIBIAL MUSCULAR DYSTROPHY", "Tardive Tibial Muscular Dystrophy", "tardive tibial muscular dystrophy", "Udd Markesbery Muscular Dystrophy", "Tardive tibial muscular dystrophy", "Udd-Markesbery Muscular Dystrophy", "TIBIAL MUSCULAR DYSTROPHY, TARDIVE", "Muscular Dystrophy, Udd-Markesbery", "Tibial Muscular Dystrophy, Tardive", "tibial muscular dystrophy, tardive", "Tibial muscular dystrophy (disorder)", "Finnish-Markesbery Muscular Dystrophy", "Finnish Markesbery Muscular Dystrophy", "Distal Myopathy Markesbery Griggs Type", "Muscular Dystrophy, Finnish-Markesbery", "Distal Myopathy Markesbery-Griggs Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tibial muscular dystrophy", "shortest_name_length": 3}
{"curie": "UMLS:C5237759", "names": ["Metastatic Primary Malignant Central Nervous System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Primary Malignant Central Nervous System Neoplasm", "shortest_name_length": 60}
{"curie": "MONDO:0045004", "names": ["skeletal ligament disorder", "disease of skeletal ligament", "disorder of skeletal ligament", "skeletal ligament disease or disorder", "disease or disorder of skeletal ligament"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skeletal ligament disorder", "shortest_name_length": 26}
{"curie": "UMLS:C0750928", "names": ["Facial-Oral Apraxia", "Facial-Oral Apraxias", "Apraxia, Facial-Oral", "Apraxia, Facial Oral", "Apraxias, Facial-Oral", "Speech And Language Disorder With Orofacial Dyspraxia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Apraxia, Facial-Oral", "shortest_name_length": 19}
{"curie": "MONDO:0009066", "names": ["Juvenile cystinosis", "Cystinosis, type II", "juvenile cystinosis", "Late-onset cystinosis", "Adolescent cystinosis", "Intermediate cystinosis", "intermediate cystinosis", "Cystinosis, Intermediate", "CYSTINOSIS, INTERMEDIATE", "cystinosis, intermediate", "Juvenile nephropathic cystinosis", "juvenile nephropathic cystinosis", "Juvenile nephropathic cystinosis (disorder)", "cystinosis, late-onset juvenile or adolescent nephropathic", "cystinosis, late-onset juvenile or adolescent nephropathic type", "CYSTINOSIS, LATE-ONSET JUVENILE OR ADOLESCENT NEPHROPATHIC TYPE", "Cystinosis, Late-Onset Juvenile or Adolescent Nephropathic Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile nephropathic cystinosis", "shortest_name_length": 19}
{"curie": "UMLS:C0549393", "names": ["ALCOHOL PROBLEM", "alcohol problem", "Alcohol problem", "Alcohol Problem", "problem alcohol", "Alcohol Problems", "alcohol problems", "Alcohol problem NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alcohol Problem", "shortest_name_length": 15}
{"curie": "MONDO:0019074", "names": ["BADI", "Acute bilateral depigmentation of iris", "bilateral acute depigmentation of the iris", "Bilateral acute depigmentation of the iris", "Acute bilateral depigmentation of iris (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bilateral acute depigmentation of the iris", "shortest_name_length": 4}
{"curie": "MONDO:0008920", "names": ["Myopathic carnitine deficiency", "myopathic carnitine deficiency", "carnitine deficiency, myopathic", "CARNITINE DEFICIENCY, MYOPATHIC", "Carnitine Deficiency, Myopathic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carnitine deficiency, myopathic", "shortest_name_length": 30}
{"curie": "MONDO:0001023", "names": ["PLL", "prolymphocytic leukemia", "Prolymphocytic leukemia", "Prolymphocytic Leukemia", "leukemia prolymphocytic", "leukemia, prolymphocytic", "leukemia; prolymphocytic", "Pro-lymphocytic leukemia", "Leukemia, Prolymphocytic", "prolymphocytic; leukemia", "Prolymphocytic leukaemia", "Prolymphocytic Leukemias", "pro-lymphocytic leukemia", "Leukemias, Prolymphocytic", "Pro-lymphocytic leukaemia", "[M]Prolymphocytic leukemia", "pll prolymphocytic leukemia", "[M]Prolymphocytic leukaemia", "PLL - Prolymphocytic leukemia", "PLL - Prolymphocytic leukaemia", "Prolymphocytic leukemia (B or T)", "prolymphocytic leukemia (B or T)", "Prolymphocytic leukemia (clinical)", "Prolymphocytic leukemia (disorder)", "Prolymphocytic leukaemia (clinical)", "prolymphocytic leukemia (diagnosis)", "Prolymphocytic leukemia (B or T-cell)", "prolymphocytic leukemia (B or T-cell)", "Prolymphocytic leukemia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prolymphocytic leukemia", "shortest_name_length": 3}
{"curie": "MONDO:0016158", "names": ["paroxysmal sleep", "Gélineau disease", "GC)lineau disease", "Gelineau syndrome", "Gelineau's syndrome", "narcoleptic syndrome", "narcolepsy with cataplexy", "narcolepsy-cataplexy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "narcolepsy-cataplexy syndrome", "shortest_name_length": 16}
{"curie": "UMLS:C1695897", "names": ["Infusion site irritation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infusion site irritation", "shortest_name_length": 24}
{"curie": "MONDO:0007054", "names": ["Shoulder dimple", "Acromial dimple", "acromial dimples", "ACROMIAL DIMPLES", "Acromial dimples", "Shoulder dimples", "Bi-acromial dimples", "SUPRASPINOUS FOSSAE, CONGENITAL", "supraspinous fossae, congenital"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acromial dimples", "shortest_name_length": 15}
{"curie": "MONDO:0009791", "names": ["impairment of oral perception", "disturbance of oral sensitivity", "ORAL SENSIBILITY, DISTURBANCE OF", "oral sensibility, disturbance of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oral sensibility, disturbance of", "shortest_name_length": 29}
{"curie": "MONDO:0003312", "names": ["ovarian endometrioid stromal sarcoma", "ovary endometrioid stromal and related neoplasms", "Ovarian Endometrioid Stromal and Related Neoplasms", "ovarian endometrioid stromal and related neoplasms", "endometrioid stromal and related neoplasms of ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian endometrioid stromal and related neoplasms", "shortest_name_length": 36}
{"curie": "UMLS:C3665746", "names": ["Instillation site discharge"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Instillation site discharge", "shortest_name_length": 27}
{"curie": "MONDO:0007699", "names": ["HT", "Ht", "Hashimoto", "Hashimoto struma", "Hashimoto Struma", "HASHIMOTO STRUMA", "Hashimoto Disease", "HASHIMOTO DISEASE", "Hashimoto disease", "hashimoto disease", "Hashimoto's struma", "Hashimoto's Struma", "Disease, Hashimoto", "Disease;Hashimotos", "Hashimoto syndrome", "disease, Hashimoto", "Hashimoto Syndrome", "Hashimotos Disease", "hashimoto's struma", "Hashimotos disease", "Hashimoto's Disease", "Struma lymphomatosa", "hashimoto's disease", "Hashimotos Syndrome", "Hashimotos syndrome", "STRUMA LYMPHOMATOSA", "Hashimoto's disease", "Autoimmune myxedema", "chronic thyroiditis", "Struma lymphomatosum", "lymphomatosa; goiter", "Hashimoto's syndrome", "Autoimmune myxoedema", "struma; lymphomatosa", "Struma lymphomatosis", "Hashimoto's Syndrome", "disease, Hashimoto's", "Disease, Hashimoto's", "Hashimoto Thyroiditis", "Syndrome, Hashimoto's", "syndrome, Hashimoto's", "lymphoid; thyroiditis", "Hashimoto thyroiditis", "HASHIMOTO THYROIDITIS", "THYROIDITIS, LYMPHOID", "thyroiditis; lymphoid", "Hashimoto's syndromes", "hashimoto thyroiditis", "THYROIDITIS HASHIMOTO", "Hashimoto's Syndromes", "Autoimmune Thyroiditis", "Syndromes, Hashimoto's", "Thyroiditis, Hashimoto", "autoimmune thyroiditis", "Hashimoto; thyroiditis", "THYROID AUTOANTIBODIES", "THYROIDITIS, HASHIMOTO", "thyroiditis; Hashimoto", "syndromes, Hashimoto's", "thyroid autoantibodies", "thyroiditis, Hashimoto", "Hashimoto thyroiditides", "lymphocytic thyroiditis", "Hashimoto Thyroiditides", "Hashimoto's thyroiditis", "Hashimoto's Thyroiditis", "Lymphocytic thyroiditis", "hashimoto's thyroiditis", "Lymphocytic Thyroiditis", "Hashimoto hypothyroidism", "autoimmune thyroiditides", "lymphomatous thyroiditis", "thyroiditides, Hashimoto", "Thyroiditides, Hashimoto", "thyroiditis; lymphocytic", "lymphocytic; thyroiditis", "lymphomatous; thyroiditis", "autoimmune hypothyroidism", "Autoimmune hypothyroidism", "thyroiditis; lymphomatous", "hypothyroidism, autoimmune", "Hypothyroidism, Autoimmune", "HYPOTHYROIDISM, AUTOIMMUNE", "Hypothyroidism (autoimmune)", "Chronic lymphocytic thyroiditis", "chronic lymphocytic thyroiditis", "Chronic Lymphocytic Thyroiditis", "Thyroiditis, Chronic Lymphocytic", "Hashimoto thyroiditis (disorder)", "thyroiditis, chronic lymphocytic", "Lymphocytic Thyroiditis, Chronic", "THYROID AUTOANTIBODIES PHENOTYPE", "lymphocytic thyroiditis, chronic", "Hashimoto thyroiditis (diagnosis)", "THYROIDITIS, CHRONIC LYMPHADENOID", "Chronic Lymphocytic Thyroiditides", "chronic lymphocytic thyroiditides", "chronic; thyroiditis, lymphadenoid", "lymphocytic thyroiditides, chronic", "Thyroiditides, Chronic Lymphocytic", "Lymphocytic Thyroiditides, Chronic", "thyroiditis; chronic, lymphadenoid", "thyroiditides, chronic lymphocytic", "Autoimmune hypothyroidism (disorder)", "autoimmune hypothyroidism (diagnosis)", "THYROIDITIS CHRONIC LYMPHOCYTIC HASHIMOTOS", "Autoimmune lymphocytic chronic thyroiditis", "THYROIDITIS CHRONIC LYMPHOCYTIC <HASHIMOTOS>", "Hypothyroidism with positive thyroid antibodies", "hypothyroidism, autoimmune thyroid autoantibodies, included"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hashimoto thyroiditis", "shortest_name_length": 2}
{"curie": "MONDO:0011894", "names": ["CMT2E", "CMT2e", "CMT 2E", "Charcot Marie Tooth disease type 2E", "Charcot-Marie-Tooth Disease Type 2E", "Charcot-Marie-Tooth disease type 2E", "Charcot-Marie-Tooth disease, type 2E", "Charcot-Marie-Tooth disease, Type 2E", "Charcot-Marie-Tooth neuropathy type 2E", "Charcot-Marie-Tooth neuropathy, type 2E", "NEFL Charcot-Marie-Tooth disease type 2", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2E", "Charcot-Marie-Tooth Neuropathy, Type 2e", "Charcot-Marie-Tooth disease, axonal, Type 2E", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E", "Charcot-Marie-Tooth disease, axonal, type 2E", "Charcot-Marie-Tooth disease type 2E (diagnosis)", "autosomal dominant Charcot-Marie-Tooth disease type 2E", "Autosomal dominant Charcot-Marie-Tooth disease type 2E", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E (disorder)", "Charcot-Marie-Tooth disease type 2 caused by mutation in NEFL", "Autosomal dominant Charcot-Marie-Tooth disease type 2E (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 2E", "shortest_name_length": 5}
{"curie": "UMLS:C0851563", "names": ["Vascular Hemorrhagic Disorder", "Vascular hemorrhagic disorders", "Vascular haemorrhagic disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vascular hemorrhagic disorders", "shortest_name_length": 29}
{"curie": "MONDO:0006971", "names": ["sigmoid neoplasm", "Sigmoid Neoplasm", "Sigmoid Neoplasms", "Neoplasm, Sigmoid", "Neoplasms, Sigmoid", "sigmoid colon tumor", "tumor of sigmoid colon", "Tumor of sigmoid colon", "Sigmoid Colon Neoplasm", "sigmoid colon neoplasm", "Sigmoid Colon Neoplasms", "Tumour of sigmoid colon", "Neoplasm, Sigmoid Colon", "Neoplasms, Sigmoid Colon", "Colon Neoplasms, Sigmoid", "neoplasm of sigmoid colon", "Neoplasm of sigmoid colon", "sigmoid colon neoplasm (disease)", "Neoplasm of sigmoid colon (disorder)", "neoplasm of sigmoid colon (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sigmoid neoplasm", "shortest_name_length": 16}
{"curie": "MONDO:0008134", "names": ["OAK", "OPA1", "optic atrophy 1", "Kjer optic atrophy", "optic atrophy type 1", "Kjer-type optic atrophy", "optic atrophy, juvenile", "optic atrophy, Kjer type", "autosomal dominant optic atrophy, Kjer type", "autosomal dominant optic atrophy, classic form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant optic atrophy, classic form", "shortest_name_length": 3}
{"curie": "UMLS:C5205705", "names": ["Sinonasal Adenocarcinoma, Intestinal-Type with Solid Pattern"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Adenocarcinoma, Intestinal-Type with Solid Pattern", "shortest_name_length": 60}
{"curie": "MONDO:0034820", "names": ["hyaluronidase 2 deficiency", "cleft lip and palate-craniofacial dysmorphism-congenital heart defect-deafness syndrome", "cleft lip and palate-craniofacial dysmorphism-congenital heart defect-hearing loss syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleft lip and palate-craniofacial dysmorphism-congenital heart defect-hearing loss syndrome", "shortest_name_length": 26}
{"curie": "UMLS:C0243001", "names": ["ABDOMEN ABSCESS", "abdomen abscess", "Abdomen--Abscess", "Abdominal Abscess", "Abdominal abscess", "abdominal abscess", "Abscess, Abdominal", "Abdominal Abscesses", "abdominal abscesses", "Abscesses, Abdominal", "Abdominal abscess NOS", "Abdominal abscess, NOS", "intra abdominal abscess", "Intra-Abdominal Abscess", "Intra-abdominal Abscess", "Intra-abdominal abscess", "intra-abdominal abscess", "Abscess, Intra-Abdominal", "abscess; intra-abdominal", "Abscess, Intra Abdominal", "intra-abdominal; abscess", "intra-abdominal abscesses", "Intra-Abdominal Abscesses", "abdominal abscesses intra", "Abscesses, Intra-Abdominal", "Abdominal abscess (disorder)", "abdominal abscess (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abdominal Abscess", "shortest_name_length": 15}
{"curie": "MONDO:0006336", "names": ["Ovarian Adenoacanthoma", "ovarian adenoacanthoma", "ovarian adenosquamous carcinoma", "Ovarian Adenosquamous Carcinoma", "adenosquamous carcinoma of ovary", "adenosquamous carcinoma of ovary (diagnosis)", "Ovarian Endometrioid Adenocarcinoma with Squamous Differentiation", "ovarian endometrioid adenocarcinoma with squamous differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian endometrioid adenocarcinoma with squamous differentiation", "shortest_name_length": 22}
{"curie": "UMLS:C0345319", "names": ["Hydatid Cyst", "Paratubal Cyst", "Morgagni Hydatid", "Morgagni Hydatids", "Hydatid of Morgagni", "Morgagni Hydatid Cyst", "Morgagni Hydatid Cysts", "Hydatid Cyst of Morgagni", "Cyst of hydatid of Morgagni", "Cyst of hydatid of Morgagni (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cyst of hydatid of Morgagni", "shortest_name_length": 12}
{"curie": "UMLS:C4289318", "names": ["FIGO Stage IIIA1(i) Ovarian Cancer", "FIGO Stage IIIA1(i) Ovarian Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Stage IIIA1(i) Ovarian Cancer", "shortest_name_length": 34}
{"curie": "MONDO:0016773", "names": ["atrophic LP", "Atrophic LP", "Atrophic Lichen Planus", "Atrophic lichen planus", "atrophic lichen planus", "Lichen planus, atrophic", "Lichen planus atrophicus", "Atrophic lichen planus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrophic lichen planus", "shortest_name_length": 11}
{"curie": "UMLS:C4520714", "names": ["stage II breast cancer", "Stage II Breast Cancer", "Breast Cancer Stage II", "Stage II Breast Carcinoma", "Carcinoma of Breast Stage II", "Stage II Breast Cancer AJCC v7", "Stage II Breast Cancer AJCC v6", "Carcinoma of the Breast Stage II", "Stage II Breast Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Breast Cancer AJCC v6 and v7", "shortest_name_length": 22}
{"curie": "MONDO:0012836", "names": ["SLEB12", "SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 12", "systemic lupus erythematosus, susceptibility to, 12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "systemic lupus erythematosus, susceptibility to, 12", "shortest_name_length": 6}
{"curie": "MONDO:0019201", "names": ["Hashitoxic periodic paralysis", "paralysis periodic thyrotoxic", "thyrotoxic periodic paralysis", "Thyrotoxic periodic paralysis", "thyrotoxic periodic paralysis syndrome", "Thyrotoxic periodic paralysis (disorder)", "Thyrotoxic hypokalemic periodic paralysis", "thyrotoxic hypokalemic periodic paralysis", "thyrotoxic periodic paralysis syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyrotoxic periodic paralysis", "shortest_name_length": 29}
{"curie": "MONDO:0022761", "names": ["chromosome 3 duplication syndrome", "Chromosome 3 duplication syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 3 duplication syndrome", "shortest_name_length": 33}
{"curie": "MONDO:0002137", "names": ["non-infected eyelid dermatoses", "Non-infected eyelid dermatoses", "Noninfectious dermatosis of eyelid", "noninfectious dermatoses of eyelid", "Noninfectious dermatoses of eyelid", "Non-infectious dermatosis of eyelid", "Noninfectious dermatosis of eyelid, NOS", "Noninfectious dermatosis of eyelid (disorder)", "noninfectious dermatoses of eyelid (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "noninfectious dermatoses of eyelid", "shortest_name_length": 30}
{"curie": "UMLS:C1827687", "names": ["Chemotherapy-induced neutropenia", "Chemotherapy induced neutropenia", "neutropenia drug-induced chemotherapy", "Chemotherapy-induced neutropenia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chemotherapy induced neutropenia", "shortest_name_length": 32}
{"curie": "MONDO:0000929", "names": ["Balloon cell melanoma", "balloon cell melanoma", "Balloon Cell Melanoma", "balloon cell skin melanoma", "Balloon Cell Skin Melanoma", "Balloon Cell Malignant Melanoma", "Balloon cell malignant melanoma", "balloon cell malignant melanoma", "balloon cell malignant skin melanoma", "Balloon Cell Malignant Skin Melanoma", "balloon cell cutaneous (skin) melanoma", "Balloon Cell Cutaneous (Skin) Melanoma", "balloon cell malignant melanoma of skin", "Balloon Cell Malignant Melanoma of Skin", "malignant neoplasm melanoma balloon cell", "Balloon cell malignant melanoma (disorder)", "balloon cell malignant melanoma of the skin", "Balloon Cell Malignant Melanoma of the Skin", "Balloon cell malignant melanoma (diagnosis)", "Balloon cell melanoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "balloon cell malignant melanoma", "shortest_name_length": 21}
{"curie": "MONDO:0044317", "names": ["POF13", "PREMATURE OVARIAN FAILURE 13", "premature ovarian failure 13", "primary ovarian insufficiency 13"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "premature ovarian failure 13", "shortest_name_length": 5}
{"curie": "MONDO:0004193", "names": ["childhood dysgerminoma", "Childhood Dysgerminoma", "childhood ovarian dysgerminoma", "Childhood Ovarian Dysgerminoma", "pediatric ovarian dysgerminoma", "Pediatric Ovarian Dysgerminoma", "childhood dysgerminoma of ovary", "pediatric dysgerminoma of ovary", "dysgerminoma of ovary of childhood", "Childhood Ovarian Germinomatous Germ Cell Tumor", "childhood ovarian germinomatous germ cell tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pediatric ovarian dysgerminoma", "shortest_name_length": 22}
{"curie": "MONDO:0005077", "names": ["PERTUSSIS", "Pertussis", "Pertusses", "pertussis", "Whooping Cough", "whooping cough", "Whooping cough", "Cough, Whooping", "WC - whooping cough", "WC - Whooping cough", "bordetella infection", "Bordetella infection", "Pertussis (disorder)", "pertussis (diagnosis)", "Bordetella pertussis infection", "infection; Bordetella pertussis", "Whooping cough due to B. pertussis", "bordetella caused disease pertussis", "whooping cough; Bordetella pertussis", "Bordetella; pertussis, whooping cough", "Infection due to Bordetella pertussis", "pertussis due to Bordetella pertussis", "infection due to Bordetella pertussis", "disease caused by bordetella pertussis", "Bordetella pertussis infectious disease", "Bordetella pertussis disease or disorder", "Whooping cough due to bordetella pertussis", "Whooping cough due to Bordetella pertussis", "Bordetella pertussis Infection, Respiratory", "pertussis; Bordetella pertussis, whooping cough", "Bordetella pertussis caused disease or disorder", "pertussis due to Bordetella pertussis (diagnosis)", "Whooping cough due to bordetella pertussis [B. pertussis]", "Whooping cough due to bordetella pertussis (B. pertussis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pertussis", "shortest_name_length": 9}
{"curie": "MONDO:0018258", "names": ["Angora hair nevus", "Schauder syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Angora hair nevus", "shortest_name_length": 17}
{"curie": "MONDO:0012618", "names": ["MRT20", "MRT10", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 10", "mental retardation, autosomal recessive 20", "mental retardation, autosomal recessive 10", "Mental Retardation, Autosomal Recessive 10", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 20", "mental retardation, autosomal recessive 10/20", "intellectual disability, autosomal recessive 10", "intellectual disability, autosomal recessive 20", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 20", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 10", "autosomal recessive intellectual developmental disorder 10/20"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 10", "shortest_name_length": 5}
{"curie": "UMLS:C5420276", "names": ["Head and Neck Follicular Dendritic Cell Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Head and Neck Follicular Dendritic Cell Sarcoma", "shortest_name_length": 47}
{"curie": "UMLS:C1332285", "names": ["Anaplastic (Malignant) Intracranial Meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anaplastic (Malignant) Intracranial Meningioma", "shortest_name_length": 46}
{"curie": "UMLS:C4054376", "names": ["Nephrotic Syndrome - MYO1E Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - MYO1E Associated", "shortest_name_length": 37}
{"curie": "MONDO:0008147", "names": ["OI2", "OIC", "OI type 2", "OI, type 2", "OI, TYPE II", "Vrolik disease", "Vrolik Disease", "Fetal osteoporosis", "Foetal osteoporosis", "Aplasia periostealis", "Perinatally lethal OI", "Porak-Durante syndrome", "Fetal osteopsathyrosis", "Foetal osteopsathyrosis", "Osteopsathyrosis congenita", "Fragilitas ossium congenita", "Aplasia ossea microplastica", "Osteogenesis imperfecta type 2", "Lethal osteogenesis imperfecta", "osteogenesis imperfecta type 2", "lethal osteogenesis imperfecta", "OI2A Osteogenesis imperfecta 2A", "osteogenesis imperfecta, type 2", "osteogenesis imperfecta type II", "Osteogenesis Imperfecta Type II", "Congenital periosteal dysplasia", "Osteogenesis imperfecta letalis", "Osteogenesis imperfecta type II", "Osteogenesis imperfecta, type II", "OSTEOGENESIS IMPERFECTA, TYPE II", "Osteogenesis imperfecta, type 2A", "osteogenesis imperfecta, type II", "Osteogenesis imperfecta type IIA", "OSTEOGENESIS IMPERFECTA, TYPE IIA", "osteogenesis imperfecta congenita", "Osteogenesis Imperfecta, Type IIA", "OSTEOGENESIS IMPERFECTA CONGENITA", "Osteogenesis imperfecta congenita", "Osteogenesis imperfecta, Vrolik type", "VROLIK TYPE OF OSTEOGENESIS IMPERFECTA", "Vrolik type of osteogenesis imperfecta", "Osteogenesis imperfecta, neonatal lethal", "Osteogenesis imperfecta, perinatal lethal", "Osteogenesis imperfecta type II (disorder)", "Osteogenesis imperfecta type IIA (disorder)", "osteogenesis imperfecta type II (diagnosis)", "Osteogenesis imperfecta type IIA (diagnosis)", "OI, type 2A Osteogenesis imperfecta, type 2A", "Osteogenesis imperfecta type II, dominant form", "OI, type IIA Osteogenesis imperfecta, type IIA", "Osteogenesis imperfecta, type II, recessive form", "Neonatal lethal osteogenesis imperfecta congenita", "osteogenesis imperfecta dominant perinatal lethal", "Osteogenesis imperfecta, dominant perinatal lethal", "perinatal lethal osteogenesis imperfecta congenita", "osteogenesis imperfecta recessive perinatal lethal", "Osteogenesis imperfecta, recessive perinatal lethal", "Osteogenesis imperfecta congenita neonatal lethal form", "osteogenesis imperfecta congenita perinatal lethal form", "osteogenesis imperfecta congenita, perinatal lethal form", "Osteogenesis imperfecta congenita, perinatal lethal form", "OSTEOGENESIS IMPERFECTA CONGENITA, PERINATAL LETHAL FORM", "Osteogenesis imperfecta, dominant perinatal lethal (disorder)", "Osteogenesis imperfecta, dominant perinatal lethal (diagnosis)", "Osteogenesis imperfecta, recessive perinatal lethal (disorder)", "Osteogenesis imperfecta, recessive perinatal lethal (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteogenesis imperfecta type 2", "shortest_name_length": 3}
{"curie": "MONDO:0016835", "names": ["dup(14)(q11.2)", "trisomy 14q11.2", "14q11.2 microduplication syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "14q11.2 microduplication syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0015993", "names": ["CRD", "Cone Rod Dystrophy", "Cone rod dystrophy", "cone rod dystrophy", "CONE-ROD DYSTROPHY", "Cone-Rod Dystrophy", "cone-rod dystrophy", "Cone-rod dystrophy", "Cone-Rod Dystrophies", "Cone Rod Dystrophies", "Cone-Rod Degeneration", "Cone-Rod Degenerations", "Cone Rod Degenerations", "Cone/cone-rod dystrophy", "Cone Rod Retinal Dystrophy", "Retinal Cone Rod Dystrophy", "Cone-rod retinal dystrophy", "Retinal Cone-Rod Dystrophy", "Cone-Rod Retinal Dystrophy", "cone-rod retinal dystrophy", "Retinal Dystrophy, Cone-Rod", "Cone-Rod Dystrophy, Retinal", "Retinal Cone-Rod Dystrophies", "Cone-Rod Retinal Dystrophies", "Retinal Dystrophies, Cone-Rod", "Cone-Rod Dystrophies, Retinal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cone-rod dystrophy", "shortest_name_length": 3}
{"curie": "UMLS:C0852566", "names": ["Sleep phase rhythm disturbance", "Sleep phase rhythm disturbances", "Disturbances in sleep phase rhythm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disturbances in sleep phase rhythm", "shortest_name_length": 30}
{"curie": "MONDO:0015196", "names": ["VGAM", "aneurysm galen vein", "Galen vein aneurysm", "Vein of Galen aneurysm", "vein of Galen aneurysm", "aneurysm of vein of Galen", "Vein of Galen malformation", "aneurysm of the vein of galen", "Aneurysm of the vein of Galen", "Galenic arteriovenous malformation", "Vein of Galen aneurysm malformation", "vein of Galen aneurysm malformation", "Vein of Galen aneurysmal malformation", "Ectasia or varix of the vein of Galen", "ectasia or varix of the vein of Galen", "aneurysm of vein of Galen (diagnosis)", "Aneurysm of the vein of Galen (disorder)", "vein of Galen arteriovenous malformations", "Vein of Galen arteriovenous malformations", "Median prosencephalic arteriovenous fistula"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vein of Galen aneurysm", "shortest_name_length": 4}
{"curie": "MONDO:0015630", "names": ["VWD2M", "Von Willebrand disease type 2M", "von Willebrand disease type 2M", "Type 2M von Willebrand Disease", "von Willebrand disease, type 2M", "Type IIM von Willebrand Disease", "Von Willebrand disease, type 2M", "von Willebrand Disease, Type 2M", "VON WILLEBRAND DISEASE, TYPE 2M", "von Willebrand Disease, Type IIM", "Hereditary von Willebrand disease type 2M", "von Willebrand disease type 2M (diagnosis)", "Hereditary von Willebrand disease type 2M (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "von Willebrand disease type 2M", "shortest_name_length": 5}
{"curie": "MONDO:0006264", "names": ["adenoid cystic carcinoma of Larynx", "Adenoid Cystic Carcinoma of Larynx", "adenoid cystic carcinoma of larynx", "Laryngeal Adenoid Cystic Carcinoma", "laryngeal adenoid cystic carcinoma", "Adenoid Cystic Carcinoma of the Larynx", "adenoid cystic carcinoma of the larynx", "laryngeal throat adenoid cystic cancer", "Laryngeal Throat Adenoid Cystic Cancer", "adenoid cystic carcinoma of larynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laryngeal adenoid cystic carcinoma", "shortest_name_length": 34}
{"curie": "UMLS:C0542404", "names": ["bladder neck stenosis", "Bladder neck stenosis", "Bladder Neck Stenosis", "stenosis; bladder-neck", "bladder-neck; stenosis", "Stenosis of bladder neck", "Bladder neck contracture", "bladder neck contracture", "bladder neck stenosis (diagnosis)", "Stenosis of bladder neck (disorder)", "bladder neck contracture (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stenosis of bladder neck", "shortest_name_length": 21}
{"curie": "MONDO:0013822", "names": ["ACRDYS2", "PDE4D acrodysostosis", "acrodysostosis caused by mutation in PDE4D", "acrodysostosis 2 with or without hormone resistance", "ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE", "acrodysostosis 2, with or without hormone resistance", "Acrodysostosis 2, with or without hormone resistance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acrodysostosis 2 with or without hormone resistance", "shortest_name_length": 7}
{"curie": "MONDO:0003772", "names": ["Cerebral Meningioma", "cerebral meningioma", "Cerebral meningioma", "meningioma of Cerebrum", "Meningioma of Cerebrum", "meningioma of cerebrum", "Meningioma of the Cerebrum", "meningioma of the cerebrum", "cerebral hemispheric meningioma", "Cerebral Hemispheric Meningioma", "meningioma of cerebral hemispheres", "telencephalon meningioma (disease)", "Meningioma of Cerebral Hemispheres", "meningioma (disease) of telencephalon", "meningioma of the cerebral hemispheres", "Meningioma of the Cerebral Hemispheres"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral meningioma", "shortest_name_length": 19}
{"curie": "UMLS:C4521747", "names": ["IIIB", "Stage IIIB Esophageal Squamous Cell Cancer", "Pathologic Stage IIIB Esophageal Squamous Cell Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IIIB Esophageal Squamous Cell Carcinoma AJCC v8", "shortest_name_length": 4}
{"curie": "MONDO:0012765", "names": ["LMPH1B", "LMPHM2", "LMPH1B, FORMERLY", "hereditary lymphedema IB", "lymphatic malformation 2", "LYMPHATIC MALFORMATION 2", "Lymphedema, Hereditary, IB", "lymphedema, hereditary, 1B", "LYMPHEDEMA, HEREDITARY, IB, FORMERLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphatic malformation 2", "shortest_name_length": 6}
{"curie": "UMLS:C1096154", "names": ["Kinsbourne syndrome", "Kinsbourne Syndrome", "kinsbourne syndrome", "opsoclonus myoclonus", "Opsoclonus Myoclonus", "Opsoclonus myoclonus", "Myoclonus, Opsoclonus", "encephalopathy infants myoclonic", "Infants Myoclonic Encephalopathy", "Infants Myoclonic Encephalopathies", "Myoclonic Encephalopathy of Infants", "Myoclonic encephalopathy of infants"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kinsbourne Syndrome", "shortest_name_length": 19}
{"curie": "MONDO:0020439", "names": ["Patent Oval Foramen", "open; foramen ovale", "foramen ovale patent", "patent foramen ovale", "PATENT FORAMAN OVALE", "Patent foramen ovale", "Oval Foramen, Patent", "FORAMEN OVALE PATENT", "Foramen ovale patent", "Patent Foramen Ovale", "patent foraman ovale", "foramen; ovale, open", "Foramen Ovale, Patent", "patent foramen ovales", "FORAMEN OVALE, PATENT", "Persistent foramen ovale", "nonclosure; foramen ovale", "persistent; foramen ovale", "Persistent ostium secundum", "PFO - Patent foramen ovale", "foramen; ovale, persistent", "persistent ostium secundum", "ovale; foramen, nonclosure", "secundum atrial septal defect", "patent foramen ovale (disease)", "Patent foramen ovale (disorder)", "patent foramen ovale (diagnosis)", "Atrial septal defect within oval fossa", "atrial septal defect within oval fossa", "ostium secundum type atrial septal defect", "Ostium secundum type atrial septal defect", "Defect, Patent or persistent, ostium secundum", "defect, patent or persistent, ostium secundum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "patent foramen ovale", "shortest_name_length": 19}
{"curie": "MONDO:0020463", "names": ["isolated congenital ectropion", "nonsyndromic congenital ectropion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated congenital ectropion", "shortest_name_length": 29}
{"curie": "UMLS:C0752261", "names": ["Thermal Sensation Disorder", "Thermal Sensation Disorders", "Sensation Disorder, Thermal", "Sensation Disorders, Thermal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thermal Sensation Disorders", "shortest_name_length": 26}
{"curie": "MONDO:0042971", "names": ["Congenital Herpes virus infection", "congenital herpes virus infection", "Herpesviridae infectious embryofetopathy", "Antenatal herpes simplex virus infection", "Congenital herpes simplex virus infection", "Congenital infection caused by Herpes virus", "congenital infection caused by herpes virus", "Herpesviridae caused infectious embryofetopathy", "Congenital infection caused by Herpes virus (disorder)", "Mother-to-child transmission of herpes simplex virus infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital herpes virus infection", "shortest_name_length": 33}
{"curie": "MONDO:0019152", "names": ["Oguchi disease", "Oguchi syndrome", "stationary night blindness, Oguchi type", "congenital stationary night blindness, Oguchi type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oguchi disease", "shortest_name_length": 14}
{"curie": "UMLS:C4524520", "names": ["Stage 0 Head and Neck Squamous Cell Cancer", "Stage 0 Cutaneous Squamous Cell Carcinoma of the Head and Neck AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Cutaneous Squamous Cell Carcinoma of the Head and Neck AJCC v8", "shortest_name_length": 42}
{"curie": "MONDO:0005987", "names": ["toxascariasis", "Toxascariases", "Toxascariasis", "Toxascaris infectious disease", "Toxascaris disease or disorder", "Toxascaris caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "toxascariasis", "shortest_name_length": 13}
{"curie": "UMLS:C0687754", "names": ["Newborn physiological jaundice", "physiological neonatal jaundice", "Physiologic jaundice of newborn", "Physiologic jaundice in newborn", "Physiological Neonatal Jaundice", "Jaundice, Physiological Neonatal", "Neonatal Jaundice, Physiological", "Physiological jaundice of infancy", "JAUNDICE, PHYSIOLOGIC, OF NEWBORN", "Physiologic jaundice NOS in newborn", "Physiologic jaundice in newborn, NOS", "Transient Neonatal Hyperbilirubinemia", "Transient neonatal hyperbilirubinemia", "Transient neonatal hyperbilirubinaemia", "Newborn physiological jaundice (disorder)", "physiological neonatal jaundice (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transient neonatal hyperbilirubinemia", "shortest_name_length": 30}
{"curie": "EFO:1001870", "names": ["late-onset Alzheimers disease", "late-onset Alzheimer's disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "late-onset Alzheimers disease", "shortest_name_length": 29}
{"curie": "UMLS:C0948162", "names": ["bone marrow edema", "Bone marrow edema", "Bone marrow oedema", "bone marrow oedema", "Edema of bone marrow", "Oedema of bone marrow", "Edema of bone marrow (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Edema of bone marrow", "shortest_name_length": 17}
{"curie": "MONDO:0035775", "names": ["CCNK-related neurodevelopmental disorder-severe intellectual disability-facial dysmorphism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CCNK-related neurodevelopmental disorder-severe intellectual disability-facial dysmorphism syndrome", "shortest_name_length": 99}
{"curie": "MONDO:0012295", "names": ["C5D", "C5 Deficiency", "C5 DEFICIENCY", "C5 deficiency", "Leiner's disease", "C5 complement deficiency", "Complement 5 dysfunction", "COMPLEMENT COMPONENT 5 DEFICIENCY", "Complement component 5 deficiency", "complement component 5 deficiency", "Complement 5 dysfunction (disorder)", "complement deficiency caused by mutation in C5", "Dysfunction of the fifth component of complement (C5)", "dysfunction of the fifth component of complement (C5)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complement component 5 deficiency", "shortest_name_length": 3}
{"curie": "MONDO:0800135", "names": ["congenital emphysematous lung disease due to Filamin A loss-of-function variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital emphysematous lung disease due to Filamin A loss-of-function variant", "shortest_name_length": 79}
{"curie": "UMLS:C5418184", "names": ["Stage 0 Low Grade Appendiceal Mucinous Neoplasm (LAMN)", "Stage 0 Low-Grade Appendix Mucinous Neoplasm (LAMN) AJCC v8", "Stage 0 Low Grade Appendix Mucinous Neoplasm (LAMN) AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Low Grade Appendix Mucinous Neoplasm (LAMN) AJCC v8", "shortest_name_length": 54}
{"curie": "MONDO:0004986", "names": ["Bladder Cancer", "bladder cancer", "CARCINOMA BLADDER", "carcinoma bladder", "Bladder carcinoma", "Cancer of Bladder", "Bladder Carcinoma", "BLADDER CARCINOMA", "Carcinoma;bladder", "Carcinoma bladder", "cancer of bladder", "bladder carcinoma", "CARCINOMA OF BLADDER", "Carcinoma of Bladder", "carcinoma of bladder", "Carcinoma of bladder", "Bladder carcinoma NOS", "cancer of the bladder", "Cancer of the Bladder", "urinary bladder cancer", "Urinary Bladder Cancer", "Carcinoma of the Bladder", "carcinoma of the bladder", "Cancer of Urinary Bladder", "Urinary Bladder Carcinoma", "URINARY BLADDER CARCINOMA", "bladder carcinoma urinary", "Carcinoma urinary bladder", "urinary bladder carcinoma", "CARCINOMA URINARY BLADDER", "cancer of urinary bladder", "BLADDER CANCER, CARCINOMA", "Urinary bladder carcinoma", "obsolete_bladder carcinoma", "Carcinoma of Urinary Bladder", "carcinoma of urinary bladder", "Cancer of the Urinary Bladder", "cancer of the urinary bladder", "Carcinoma of bladder (disorder)", "carcinoma of the urinary bladder", "Carcinoma of the Urinary Bladder", "carcinoma of bladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urinary bladder carcinoma", "shortest_name_length": 14}
{"curie": "UMLS:C0435002", "names": ["Ligament sprain", "ligament sprain", "Sprain;ligament", "ligaments sprain", "ligament sprains", "ligament sprained", "sprain of ligament", "ligaments sprained", "Sprain of ligament", "partial ligament tear", "Sprain of ligament (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sprain of ligament", "shortest_name_length": 15}
{"curie": "UMLS:C0263641", "names": ["Epidermal hyperplasia", "Epidermal Hyperplasia", "epithelial; hyperplasia, skin", "hyperplasia; epithelial, skin", "Epithelial hyperplasia of skin", "Epithelial hyperplasia of skin, NOS", "Epithelial hyperplasia of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epithelial hyperplasia of skin", "shortest_name_length": 21}
{"curie": "MONDO:0100443", "names": ["RDH5 retinopathy", "fundus albipunctatus", "RDH5-related retinopathy", "pigmentary retinal dystrophy", "retinitis punctata albescens"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "RDH5-related retinopathy", "shortest_name_length": 16}
{"curie": "UMLS:C4521748", "names": ["Stage IV Esophageal Squamous Cell Cancer", "Pathologic Stage IV Esophageal Squamous Cell Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IV Esophageal Squamous Cell Carcinoma AJCC v8", "shortest_name_length": 40}
{"curie": "UMLS:C2887096", "names": ["Sepsis due to Pseudomonas", "Sepsis caused by Pseudomonas", "Sepsis caused by Pseudomonas (disorder)", "Severe sepsis with acute organ dysfunction caused by Pseudomonas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sepsis due to Pseudomonas", "shortest_name_length": 25}
{"curie": "MONDO:0054847", "names": ["FAME7", "BAFME7", "FCMTE7", "familial adult myoclonic epilepsy 7", "epilepsy, FAMILIAL ADULT myoclonic, 7", "EPILEPSY, FAMILIAL ADULT MYOCLONIC, 7", "epilepsy, familial adult myoclonic, 7", "BENIGN ADULT FAMILIAL MYOCLONIC EPILEPSY 7", "benign adult familial myoclonic epilepsy 7", "benign Adult Familial myoclonic epilepsy 7", "familial cortical myoclonic tremor and epilepsy 7", "CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 7", "cortical myoclonic tremor with epilepsy, Familial, 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, familial adult myoclonic, 7", "shortest_name_length": 5}
{"curie": "MONDO:0019393", "names": ["idiopathic bile acid malabsorption", "idiopathic malabsorption due to bile acid synthesis defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic malabsorption due to bile acid synthesis defects", "shortest_name_length": 34}
{"curie": "MONDO:0005084", "names": ["mental disorder", "mental process disease", "disorder of mental process", "mental or behavioural disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mental disorder", "shortest_name_length": 15}
{"curie": "MONDO:0014608", "names": ["MFDA", "Mandibulofacial dysostosis with alopecia", "mandibulofacial dysostosis with alopecia", "MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA", "MFDA - mandibulofacial dysostosis with alopecia", "Mandibulofacial dysostosis with alopecia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mandibulofacial dysostosis with alopecia", "shortest_name_length": 4}
{"curie": "MONDO:0015236", "names": ["aortic arch defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic arch defects", "shortest_name_length": 19}
{"curie": "UMLS:C1332056", "names": ["AIDS-Related Plasmablastic Lymphoma of Mucosa Site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Plasmablastic Lymphoma of Mucosa Site", "shortest_name_length": 50}
{"curie": "UMLS:C1336382", "names": ["Stage IVB Mouth Carcinoma", "Stage IVB Oral Cavity Cancer", "Stage IVB Carcinoma of Mouth", "Stage IVB Oral Cavity Carcinoma", "Stage IVB Carcinoma of the Mouth", "Stage IVB Carcinoma of Oral Cavity", "Stage IVB Oral Cavity Cancer AJCC v6", "Stage IVB Oral Cavity Cancer AJCC v7", "Stage IVB Carcinoma of the Oral Cavity", "Stage IVB Oral Cavity Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Oral Cavity Cancer AJCC v6 and v7", "shortest_name_length": 25}
{"curie": "MONDO:0013115", "names": ["MACS SYNDROME", "RIN2 syndrome", "MACS Syndrome", "MACS syndrome", "RIN2 deficiency", "macrocephaly, alopecia, cutis laxa, and scoliosis", "Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis", "MACROCEPHALY, ALOPECIA, CUTIS LAXA, AND SCOLIOSIS", "macrocephaly-alopecia-cutis laxa-scoliosis syndrome", "Macrocephaly-alopecia-cutis laxa-scoliosis syndrome", "Macrocephaly, alopecia, cutis laxa, scoliosis syndrome", "MACS (macrocephaly, alopecia, cutis laxa, scoliosis) syndrome", "Macrocephaly, alopecia, cutis laxa, scoliosis syndrome (disorder)", "TALL FOREHEAD, SPARSE HAIR, SKIN HYPEREXTENSIBILITY, AND SCOLIOSIS", "tall forehead, sparse hair, skin hyperextensibility, and scoliosis", "Tall forehead-sparse hair-skin hyperextensibility-scoliosis syndrome", "tall forehead-sparse hair-skin hyperextensibility-scoliosis syndrome", "Tall forehead, sparse hair, skin hyperextensibility, scoliosis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "RIN2 syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0800174", "names": ["encephalitis, acute, infection-induced, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephalitis, acute, infection-induced, susceptibility to", "shortest_name_length": 57}
{"curie": "MONDO:0001943", "names": ["Quartan Malaria", "Quartan malaria", "quartan malaria", "Malaria, quartan", "malaria; quartan", "Malariae malaria", "malaria; malariae", "quartan; malarial", "malariae; malarial", "Plasmodium; malariae", "Quartan malaria (disorder)", "Plasmodium malariae malaria", "malaria; Plasmodium malariae", "malaria by Plasmodium malariae", "Malaria by Plasmodium malariae", "Plasmodium malariae malaria NOS", "malaria due to plasmodium malariae", "malaria due to plasmodium malariae (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Plasmodium malariae malaria", "shortest_name_length": 15}
{"curie": "UMLS:C5419619", "names": ["Advanced Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Hodgkin Lymphoma", "shortest_name_length": 25}
{"curie": "MONDO:0018989", "names": ["acute pancreatitis recurrent", "acute recurrent pancreatitis", "Acute recurrent pancreatitis", "Recurrent Acute Pancreatitis", "Recurrent acute pancreatitis", "PANCREATITIS ACUTE RECURRENT", "recurrent acute pancreatitis", "Acute Recurrent Pancreatitis", "acute (recurrent) pancreatitis", "Acute recurrent pancreatitis (disorder)", "acute recurrent pancreatitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "recurrent acute pancreatitis", "shortest_name_length": 28}
{"curie": "MONDO:0060659", "names": ["NDPLHS", "neurodevelopmental disorder with poor language and loss of hand skills", "NEURODEVELOPMENTAL DISORDER WITH POOR LANGUAGE AND LOSS OF HAND SKILLS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with poor language and loss of hand skills", "shortest_name_length": 6}
{"curie": "MONDO:0012907", "names": ["SCOLIOSIS, ARACHNODACTYLY, AND BLINDNESS", "scoliosis, arachnodactyly, and blindness", "Scoliosis, Arachnodactyly, And Blindness", "Blindness-scoliosis-arachnodactyly syndrome", "Blindness, scoliosis, arachnodactyly syndrome", "blindness - scoliosis - arachnodactyly syndrome", "Blindness, scoliosis, arachnodactyly syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blindness - scoliosis - arachnodactyly syndrome", "shortest_name_length": 40}
{"curie": "UMLS:C0233718", "names": ["Pressured speech", "pressured speech", "Pressured Speech", "pressure of speech", "Pressure of speech", "speech rate pressured", "Pressure of speech (finding)", "speech rate pressured (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pressure of speech", "shortest_name_length": 16}
{"curie": "MONDO:0054771", "names": ["KTCN9", "keratoconus 9", "KERATOCONUS 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratoconus 9", "shortest_name_length": 5}
{"curie": "UMLS:C3272431", "names": ["Preinvasive Neoplasm of the Ampullary Region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Preinvasive Neoplasm of the Ampullary Region", "shortest_name_length": 44}
{"curie": "UMLS:C1336863", "names": ["Undifferentiated Prostate Carcinoma", "Prostate Undifferentiated Carcinoma", "Undifferentiated Prostatic Carcinoma", "Undifferentiated Carcinoma of Prostate", "Undifferentiated Carcinoma of the Prostate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Undifferentiated Carcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C1515302", "names": ["Testicular Tumor of the Thecoma/Fibroma Group"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular Tumor of the Thecoma/Fibroma Group", "shortest_name_length": 45}
{"curie": "MONDO:0008347", "names": ["PPH1", "IFPAH", "pulmonary hypertension, primary, 1", "pulmonary hypertension, primary, type 1", "idiopathic and/or familial pulmonary arterial hypertension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic and/or familial pulmonary arterial hypertension", "shortest_name_length": 4}
{"curie": "MONDO:0035763", "names": ["Idiopathic non-lupus FHN", "idiopathic non-lupus full-house nephropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic non-lupus full-house nephropathy", "shortest_name_length": 24}
{"curie": "MONDO:0002620", "names": ["Osteosarcoma localized", "Localized Osteosarcoma", "Osteosarcoma localised", "localized osteosarcoma", "localised osteosarcoma", "osteosarcoma, localized", "Osteosarcoma, Localized", "Osteogenic sarcoma localized", "Osteogenic sarcoma localised", "localised Osteogenic sarcoma", "localized osteogenic sarcoma", "Localized Osteogenic Sarcoma", "localized Osteogenic sarcoma", "osteogenic sarcoma, localized", "sarcoma, localized osteogenic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "localized osteosarcoma", "shortest_name_length": 22}
{"curie": "MONDO:0015951", "names": ["photogénodermatose", "photogenodermatosis", "genetic photosensitivity", "hereditary photodermatosis", "genetic skin photosensitivity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary photodermatosis", "shortest_name_length": 18}
{"curie": "MONDO:0005642", "names": ["Atopic conjunctivitis", "Atopic Conjunctivitis", "atopic conjunctivitis", "Conjunctivitis, Atopic", "atopic; conjunctivitis", "conjunctivitis; atopic", "ALLERGIC CONJUNCTIVITIS", "Atopic Conjunctivitides", "Allergic conjunctivitis", "allergic conjunctivitis", "Conjunctivitis allergic", "CONJUNCTIVITIS ALLERGIC", "Conjunctivitis;allergic", "conjunctivitis allergic", "Allergic Conjunctivitis", "Conjunctivitides, Atopic", "allergic; conjunctivitis", "Conjunctivitis, Allergic", "conjunctivitis; allergic", "CONJUNCTIVITIS, ALLERGIC", "Allergic Conjunctivitides", "Conjunctivitides, Allergic", "Atopic conjunctivitis (disorder)", "allergic conjunctivitis (disease)", "Allergic conjunctivitis (disorder)", "Allergic conjunctivitis (diagnosis)", "allergic form of conjunctivitis (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atopic conjunctivitis", "shortest_name_length": 21}
{"curie": "MONDO:0004724", "names": ["submandibular gland cancer", "Submandibular Gland Cancer", "submandibular gland carcinoma", "Submandibular Gland Carcinoma", "cancer of submandibular gland", "Carcinoma of Submandibular Gland", "Carcinoma of submandibular gland", "carcinoma of submandibular gland", "Malignant Submandibular Gland Tumor", "Carcinoma of the Submandibular Gland", "carcinoma of the submandibular gland", "malignant tumor of submandibular gland", "Malignant Tumor of Submandibular Gland", "Malignant Submandibular Gland Neoplasm", "Malignant tumor of submandibular gland", "malignant submandibular gland neoplasm", "Malignant tumour of submandibular gland", "malignant neoplasm of submaxillary gland", "Malignant neoplasm of submaxillary gland", "malignant neoplasm of submandibular gland", "Malignant Neoplasm of Submandibular Gland", "Malignant neoplasm of submandibular gland", "malignant tumor of the Submandibular gland", "Malignant Tumor of the Submandibular Gland", "malignant tumor of the submandibular gland", "Carcinoma of submandibular gland (disorder)", "Carcinoma of submandibular gland (diagnosis)", "Malignant Neoplasm of the Submandibular Gland", "Malignant tumor of submandibular gland (disorder)", "malignant neoplasm of submandibular gland (diagnosis)", "malignant salivary gland neoplasm submandibular carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "submandibular gland cancer", "shortest_name_length": 26}
{"curie": "MONDO:0016738", "names": ["primary germ cell tumor of CNS", "primary germ cell tumor of central nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary germ cell tumor of central nervous system", "shortest_name_length": 30}
{"curie": "MONDO:0015834", "names": ["didelphys", "extra; uterus", "Double uterus", "Didelphic Uteri", "Uterus didelphys", "uterus didelphic", "didelphis uterus", "Uterus didelphis", "didelphys uterus", "UTERUS DIDELPHUS", "Didelphic Uterus", "didelphic uterus", "Didelphys uterus", "Uterus didelphus", "uterus didelphys", "Didelphic uterus", "uterus didelphus", "didelphus uterus", "Uterus, Didelphic", "Uterine didelphys", "uterus; didelphys", "Uterine Didelphys", "didelphys; uterus", "doubling of uterus", "Bicervical bicornuate uterus", "doubling of uterus (diagnosis)", "doubling of uterus (obstetric)", "Congenital duplication of uterus", "doubling of uterus (obstetric) (diagnosis)", "Congenital duplication of uterus (disorder)", "congenital abnormality of uterus, doubling of uterus", "congenital uterine abnormality, doubling of uterus (obstetric)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "didelphys uterus", "shortest_name_length": 9}
{"curie": "UMLS:C0595916", "names": ["renal toxicity", "RENAL TOXICITY", "TOXICITY RENAL", "Toxicity renal", "NEPHROTOXICITY", "nephrotoxicity", "Nephrotoxicity", "Renal Toxicity", "Toxic nephrosis", "Kidney Toxicity", "nephropathy toxic", "Toxic nephropathy", "Nephropathy toxic", "toxic nephropathy", "NEPHROPATHY TOXIC", "TOXIC NEPHROPATHY", "nephropathy; toxic", "toxic; nephropathy", "Toxic nephropathy, NOS", "Toxic nephropathy (disorder)", "toxic nephropathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Toxic nephropathy", "shortest_name_length": 14}
{"curie": "UMLS:C0009983", "names": ["Coprophagy", "coprophagy", "Coprophagia", "coprophagia", "eating feces", "feces eating", "Eating feces", "Eating faeces", "eating faeces", "Eating feces (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Coprophagia", "shortest_name_length": 10}
{"curie": "MONDO:0010709", "names": ["Wsn", "WSN", "BGMR", "WSMN", "Waisman syndrome", "WAISMAN SYNDROME", "WAISMAN syndrome", "Waisman Syndrome", "Laxova-Opitz syndrome", "Laxova Opitz syndrome", "Waisman-Laxova syndrome", "Laxova Brown hogan syndrome", "Laxova Brown Hogan syndrome", "Waisman syndrome, X-linked recessive", "basal ganglia disorder with mental retardation", "Basal ganglia disorder with mental retardation", "basal ganglion disorder with mental retardation", "Basal Ganglion Disorder With Mental Retardation", "BASAL GANGLION DISORDER WITH MENTAL RETARDATION", "Parkinsonism, early onset with mental retardation", "Parkinsonism, early-onset, with mental retardation", "Parkinsonism, Early-Onset, With Mental Retardation", "PARKINSONISM, EARLY-ONSET, WITH MENTAL RETARDATION", "basal ganglion disorder-mental retardation syndrome", "basal ganglia disorder with intellectual disability", "basal ganglion disorder with intellectual disability", "early onset parkinsonism-mental retardation syndrome", "Parkinsonism, early onset with intellectual disability", "Parkinsonism, early-onset, with intellectual disability", "Early-onset parkinsonism-intellectual disability syndrome", "early-onset parkinsonism-intellectual disability syndrome", "basal ganglion disorder-mental retardation (BGMR) syndrome", "Early onset parkinsonism and intellectual disability syndrome", "Early onset Parkinsonism and intellectual disability syndrome", "X-linked recessive basal ganglia disorder with mental retardation", "Parkinson disease young onset and intellectual disability syndrome", "X-linked recessive basal ganglia disorder with intellectual disability", "Early onset parkinsonism and intellectual disability syndrome (disorder)", "Early onset Parkinsonism and intellectual disability syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early-onset parkinsonism-intellectual disability syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0002008", "names": ["Labrynthitis", "LABYRINTHITIS", "Labyrinthitis", "labyrinthitis", "Otitis interna", "otitis interna", "Otitis Interna", "OTITIS INTERNA", "interna; otitis", "otitis; interna", "Labyrinthitides", "Labyrinthitis NOS", "Labyrinthitis, NOS", "inner ear infection", "Inner Ear Infection", "hyperemia; labyrinth", "labyrinth; hyperemia", "Inner ear inflammation", "Internal Ear Infection", "inflammation; inner ear", "inner ear; inflammation", "Labyrinthitis (disorder)", "internal ear inflammation", "labyrinthitis (diagnosis)", "Infectious Otitis Interna", "Inflammation of inner ear", "Labyrinthitis, unspecified", "inflammation of internal ear", "Labyrinthitis, unspecified ear", "Inflammation of the inner ear(s)", "Inflammation of inner ear (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "labyrinthitis", "shortest_name_length": 12}
{"curie": "UMLS:C4525731", "names": ["Posterior Subcapsular Cataract Grade 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Posterior Subcapsular Cataract Grade 1", "shortest_name_length": 38}
{"curie": "MONDO:0024563", "names": ["IIAE1", "UNC93B1 herpes simplex encephalitis", "HERPES SIMPLEX ENCEPHALITIS, SUSCEPTIBILITY TO, 1", "herpes simplex encephalitis, susceptibility to, 1", "herpes simplex encephalitis caused by mutation in UNC93B1", "encephalopathy, acute, infection-induced, susceptibility to, 1", "ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 1", "encephalopathy, acute, infection-induced (Herpes-specific), susceptibility to, 1", "encephalopathy, acute, infection-induced (HERPES-specific), susceptibility to, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "herpes simplex encephalitis, susceptibility to, 1", "shortest_name_length": 5}
{"curie": "MONDO:0020840", "names": ["PAPHG", "IMD100", "pulmonary alveolar proteinosis with hypogammaglobulinemia", "PULMONARY ALVEOLAR PROTEINOSIS WITH HYPOGAMMAGLOBULINEMIA", "IMMUNODEFICIENCY 100 WITH PULMONARY ALVEOLAR PROTEINOSIS AND HYPOGAMMAGLOBULINEMIA", "immunodeficiency (due to OAS1 gain-of-function variant) with pulmonary alveolar proteinosis and hypogammaglobulinemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary alveolar proteinosis with hypogammaglobulinemia", "shortest_name_length": 5}
{"curie": "MONDO:0006978", "names": ["infarct spleen", "Spleen infarct", "SPLEEN INFARCT", "spleen infarct", "splenic infarct", "SPLENIC INFARCT", "Splenic infarct", "Splenic Infarct", "infarcted spleen", "Infarct, Splenic", "Splenic Infarcts", "splenic infarcts", "infarcts splenic", "infarction spleen", "Spleen infarction", "spleen infarction", "Infarcts, Splenic", "SPLENIC INFARCTION", "Splenic infarction", "spleen; infarction", "Infarction;splenic", "Splenic Infarction", "infarction; spleen", "splenic infarction", "infarction splenic", "Splenic Infarctions", "Infarction, Splenic", "Infarctions, Splenic", "Infarction of spleen", "infarct of the spleen", "Infarct of the Spleen", "splenic infarct (diagnosis)", "Splenic infarction (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "splenic infarction", "shortest_name_length": 14}
{"curie": "UMLS:C1519175", "names": ["Salivary Gland Myoepithelial Tumor", "Salivary Gland Myoepithelial Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Salivary Gland Myoepithelial Tumor", "shortest_name_length": 34}
{"curie": "UMLS:C1880323", "names": ["DHPLN", "NEPHROBLASTEMATOSIS", "diffuse hyperplastic perilobar nephroblastomatosis", "Diffuse Hyperplastic Perilobar Nephroblastomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse Hyperplastic Perilobar Nephroblastomatosis", "shortest_name_length": 5}
{"curie": "MONDO:0017528", "names": ["preaxial polydactyly type 3, bilateral", "polydactyly of an index finger, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polydactyly of an index finger, bilateral", "shortest_name_length": 38}
{"curie": "MONDO:0018066", "names": ["47,XXX", "47,Xxx", "X; triple", "trisomy X", "trisomy x", "Trisomy X", "x trisomy", "X trisomy", "triple; X", "super female", "Super female", "XXX syndrome", "xxx syndrome", "females super", "trisomy type X", "47,XXX syndrome", "47,XXX Syndrome", "triple-X female", "47 XXX syndrome", "Triple X female", "Triple-X female", "triple x female", "females triple x", "karyotype 47,XXX", "Karyotype 47,XXX", "karyotype; 47,XXX", "syndrome triple x", "triple-x syndrome", "Triple X Syndrome", "Triple X syndrome", "Triplo-X syndrome", "Triplo X syndrome", "triplo-x syndrome", "triple x syndrome", "triple-X syndrome", "triplo x syndrome", "Karyotype 47, XXX", "triple X syndrome", "triplo-X syndrome", "syndrome; triple X", "triple X; syndrome", "trisomy X syndrome", "trisomy x syndrome", "Trisomy X syndrome", "intersex complex 47,XXX", "chromosome XXX syndrome", "47,XXX complex intersex", "chromosome xxx syndrome", "xxx chromosome syndrome", "Triple X syndrome, female", "chromosome 47,XXX syndrome", "triple-X chromosome syndrome", "karyotype 47,XXX (diagnosis)", "Triple-X chromosome syndrome", "triple X syndrome (diagnosis)", "Trisomy X syndrome (disorder)", "47,XXX complex intersex (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trisomy X", "shortest_name_length": 6}
{"curie": "MONDO:0100409", "names": ["AML, t(3;5)(q25;q34)", "AML with Myelodysplasia-Related Changes", "AML with Myelodysplasia-related Changes", "acute myeloid leukemia, t(3;5)(q25;q34)", "AML with myelodysplasia-related changes", "Acute Myeloid Leukemia with Myelodysplasia-Related Changes", "Acute myeloid leukemia with myelodysplasia-related changes", "acute myeloid leukemia with myelodysplasia-related changes", "Acute myeloid leukaemia with myelodysplasia-related changes", "Acute myeloid leukemia without prior myelodysplastic syndrome", "Acute myeloid leukaemia without prior myelodysplastic syndrome", "Acute myeloid leukemia with myelodysplasia-related changes (disorder)", "Acute myeloid leukemia with multilineage dysplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, t(3;5)(q25;q34)", "shortest_name_length": 20}
{"curie": "UMLS:C4525125", "names": ["Stage IIIA Colon Cancer", "stage IIIA colon cancer", "Stage IIIA Colon Cancer AJCC v8", "malignant large intestine neoplasm stage IIIa", "malignant large intestine neoplasm stage IIIa (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Colon Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "MONDO:0012219", "names": ["autosomal recessive spondyloepiphyseal dysplasia tarda Leroy-Spranger type", "spondyloepiphyseal dysplasia tarda, autosomal recessive, Leroy-Spranger type", "Spondyloepiphyseal Dysplasia Tarda, Autosomal Recessive, Leroy-Spranger Type", "SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE, LEROY-SPRANGER TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepiphyseal dysplasia tarda, autosomal recessive, Leroy-Spranger type", "shortest_name_length": 74}
{"curie": "UMLS:C0740364", "names": ["Benign Ovarian Cyst", "Benign ovarian cyst", "Cyst;ovarian;benign", "ovarian cyst benign", "OVARY, CYST, BENIGN", "OVARIAN CYST BENIGN", "benign ovarian cyst", "benign cysts ovarian", "Benign Cyst of Ovary", "Benign cyst of ovary", "Benign Cyst of the Ovary", "Benign cyst of ovary (disorder)", "Benign cyst of ovary (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign cyst of ovary", "shortest_name_length": 19}
{"curie": "MONDO:0013330", "names": ["AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA", "agenesis of the corpus callosum and congenital lymphedema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "agenesis of the corpus callosum and congenital lymphedema", "shortest_name_length": 57}
{"curie": "UMLS:C1333385", "names": ["Endobronchial Hamartoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endobronchial Hamartoma", "shortest_name_length": 23}
{"curie": "MONDO:0017107", "names": ["isolated cerebellar vermis agenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated cerebellar vermis agenesis", "shortest_name_length": 35}
{"curie": "MONDO:0002687", "names": ["SMAS", "Cast Syndrome", "Cast syndrome", "cast syndrome", "CAST SYNDROME", "Syndrome, Cast", "Wilkie syndrome", "Wilkie Syndrome", "Syndrome, Wilkie", "Wilkie's syndrome", "DUODENUM, VASCULAR COMPRESSION", "a.mesenterica superior; syndrome", "ARTERIOMESENTERIC DUODENAL ILEUS", "superior mesenteric artery syndrome", "SUPERIOR MESENTERIC ARTERY SYNDROME", "Superior mesenteric artery syndrome", "Superior Mesenteric Artery Syndrome", "syndrome; superior mesenteric artery", "vascular compression of the duodenum", "Mesenteric Duodenal Compression Syndrome", "Duodenal Compression Syndrome, Mesenteric", "Mesenteric vascular insufficiency syndrome", "SMAS - Superior mesenteric artery syndrome", "mesenteric; vascular insufficiency syndrome", "syndrome; mesenteric vascular insufficiency", "superior mesenteric artery syndromic disease", "Superior mesenteric artery syndrome (disorder)", "syndromic disease of superior mesenteric artery", "superior mesenteric artery syndrome (diagnosis)", "Arteriomesenteric duodenal compression syndrome", "DUODENUM, OCCLUSION BY SUPERIOR MESENTERIC ARTERY", "Chronic intermittent arteriomesenteric occlusion of the duodenum syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "superior mesenteric artery syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0012678", "names": ["ATFB5", "atrial fibrillation, familial, 5", "Atrial Fibrillation, Familial, 5", "ATRIAL FIBRILLATION, FAMILIAL, 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial fibrillation, familial, 5", "shortest_name_length": 5}
{"curie": "MONDO:0012958", "names": ["MS4", "multiple sclerosis, susceptibility to, 4", "MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO, 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple sclerosis, susceptibility to, 4", "shortest_name_length": 3}
{"curie": "MONDO:0012199", "names": ["Ppcd2", "PPCD2", "posterior polymorphous corneal dystrophy 2", "corneal dystrophy, posterior polymorphous 2", "corneal dystrophy, POSTERIOR polymorphous, 2", "Corneal Dystrophy, Posterior Polymorphous, 2", "CORNEAL DYSTROPHY, POLYMORPHOUS POSTERIOR, 2", "CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 2", "COL8A2 posterior polymorphous corneal dystrophy", "posterior polymorphous corneal dystrophy type 2", "corneal dystrophy, posterior polymorphous, type 2", "posterior polymorphous corneal dystrophy caused by mutation in COL8A2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "posterior polymorphous corneal dystrophy 2", "shortest_name_length": 5}
{"curie": "UMLS:C4054579", "names": ["Malignant Fibrohistiocytic Neoplasm", "Malignant fibrohistiocytic neoplasm", "Malignant fibrohistiocytic neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant fibrohistiocytic neoplasm", "shortest_name_length": 35}
{"curie": "UMLS:C1334996", "names": ["Non-Neoplastic Bladder Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Bladder Disorder", "shortest_name_length": 31}
{"curie": "MONDO:0014062", "names": ["PEOA6", "DNA2-related mitochondrial DNA deletion syndrome", "mtDNA deletion syndrome with progressive myopathy", "mtDNA deletion syndrome with limb-girdle weakness", "autosomal dominant progressive external ophthalmoplegia 6", "progressive external ophthalmoplegia, autosomal dominant 6", "PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL DOMINANT 6", "mitochondrial DNA deletion syndrome with limb-girdle weakness", "mitochondrial DNA deletion syndrome with progressive myopathy", "autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 6", "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 6", "PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 6", "PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT, 6", "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant type 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial DNA deletion syndrome with progressive myopathy", "shortest_name_length": 5}
{"curie": "UMLS:C0919907", "names": ["Pleural infection", "pleural infection", "Pleural Infection", "infections pleural", "Pleural infection NOS", "pleural infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pleural Infection", "shortest_name_length": 17}
{"curie": "MONDO:0019760", "names": ["congenital limb amputation", "TERMINAL TRANSVERSE DEFECTS OF ARM", "Terminal Transverse Defects of Arm", "terminal transverse defects of arm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "terminal transverse defects of arm", "shortest_name_length": 26}
{"curie": "MONDO:0015021", "names": ["HADDS", "hypotonia, ataxia, and delayed development syndrome", "HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME", "hypotonia, ataxia, and delayed development syndrome; HADDS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotonia, ataxia, and delayed development syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0016043", "names": ["isolated cleft lip", "isolated cleft lip (disease)", "nonsyndromic cleft lip (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated cleft lip", "shortest_name_length": 18}
{"curie": "UMLS:C2697518", "names": ["Grade 1 Diffuse Follicular Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade 1 Diffuse Follicular Lymphoma", "shortest_name_length": 35}
{"curie": "MONDO:0008503", "names": ["Worster Drought syndrome", "Worster-Drought syndrome", "WORSTER-DROUGHT SYNDROME", "Worster-Drought Syndrome", "suprabulbar paresis congenital", "Congenital suprabulbar paresis", "congenital suprabulbar paresis", "Suprabulbar paresis congenital", "suprabulbar paresis, congenital", "SUPRABULBAR PARESIS, CONGENITAL", "Suprabulbar Paresis, Congenital", "Congenital suprabulbar paresis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Worster-Drought syndrome", "shortest_name_length": 24}
{"curie": "UMLS:C0855189", "names": ["Stage II Bladder Squamous Cell Cancer", "Bladder squamous cell carcinoma stage II", "Squamous cell bladder carcinoma stage II", "Stage II Bladder Squamous Cell Carcinoma", "Squamous cell carcinoma of the bladder stage II", "Stage II Bladder Squamous Cell Carcinoma AJCC v7", "Stage II Bladder Squamous Cell Carcinoma AJCC v6", "Stage II Bladder Squamous Cell Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder squamous cell carcinoma stage II", "shortest_name_length": 37}
{"curie": "MONDO:0006729", "names": ["Discrete Subaortic Stenoses", "Discrete Subaortic Stenosis", "discrete subaortic stenosis", "Stenoses, Discrete Subaortic", "Subaortic Stenosis, Discrete", "Stenosis, Discrete Subaortic", "Subaortic Stenoses, Discrete"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "discrete subaortic stenosis", "shortest_name_length": 27}
{"curie": "UMLS:C4055498", "names": ["ALL Gene Expression Subtype", "ALL by Gene Expression Profile", "ALL by Gene Expression Signature", "ALL Gene Expression Cluster Subtype", "Acute Lymphoblastic Leukemia Gene Expression Subtype", "Acute Lymphoblastic Leukemia by Gene Expression Profile", "Acute Lymphoblastic Leukemia by Gene Expression Signature"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Lymphoblastic Leukemia by Gene Expression Profile", "shortest_name_length": 27}
{"curie": "MONDO:0044083", "names": ["alternariosis", "Alternarioses", "Alternariosis", "dermal Alternariosis", "dermal Alternarioses", "Alternarioses, dermal", "Alternariosis, dermal", "cutaneous Alternariosis", "Cutaneous Alternarioses", "cutaneous Alternarioses", "Cutaneous Alternariosis", "Cutaneous alternariosis", "cutaneous alternariosis", "Alternariosis, Cutaneous", "Alternariosis, cutaneous", "Alternarioses, Cutaneous", "Alternarioses, cutaneous", "subcutaneous Alternarioses", "subcutaneous Alternariosis", "Alternariosis, subcutaneous", "Alternarioses, subcutaneous", "Cutaneous alternariosis (disorder)", "Cutaneous alternariosis (diagnosis)", "mycosis dermal cutaneous alternariosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alternariosis", "shortest_name_length": 13}
{"curie": "MONDO:0001830", "names": ["Briquet", "Briquet syndrome", "briquet syndrome", "Briquet Syndrome", "briquets syndrome", "Syndrome, Briquet", "Briquets syndrome", "Briquet's syndrome", "Briquet's disorder", "briquet's syndrome", "briquet's disorder", "Disorder;somatisation", "Somatization disorder", "somatization disorder", "somatisation disorder", "Somatisation disorder", "Somatization Disorder", "SOMATIZATION DISORDER", "disorder somatization", "somatization disorders", "Somatization Disorders", "disorders somatisation", "disorder; somatization", "somatization; disorder", "Polysomatizing disorder", "Polysomatising disorder", "Briquet's syndrome (disorder)", "Briquet's syndrome (diagnosis)", "Somatization disorder (disorder)", "somatization disorder (diagnosis)", "Polysomatizing disorder (disorder)", "Polysomatizing disorder (diagnosis)", "somatization disorder Briquet's syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "somatization disorder", "shortest_name_length": 7}
{"curie": "MONDO:0004482", "names": ["FP", "fibroosseous digital pseudotumor", "Fibroosseous Digital Pseudotumor", "fibroosseous pseudotumor of digits", "Fibroosseous Pseudotumor of Digits", "fibroosseous pseudotumor of the digits", "Fibroosseous Pseudotumor of the Digits"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibroosseous pseudotumor of the digits", "shortest_name_length": 2}
{"curie": "UMLS:C5446558", "names": ["Lacrimal Gland Reactive Lymphoid Hyperplasia", "Reactive lymphoid hyperplasia of lacrimal gland", "Reactive lymphoid hyperplasia of lacrimal gland (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reactive lymphoid hyperplasia of lacrimal gland", "shortest_name_length": 44}
{"curie": "MONDO:0030512", "names": ["SPG85", "hereditary spastic paraplegia 85", "spastic paraplegia 85 autosomal recessive", "spastic paraplegia 85, autosomal recessive", "SPASTIC PARAPLEGIA 85, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic paraplegia 85, autosomal recessive", "shortest_name_length": 5}
{"curie": "UMLS:C0856150", "names": ["hematoma spinal", "spinal hematoma", "hematomas spinal", "spinal hematoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal hematoma", "shortest_name_length": 15}
{"curie": "MONDO:0001470", "names": ["anal margin squamous cell carcinoma", "Anal margin squamous cell carcinoma", "Anal Margin Squamous Cell Carcinoma", "perianal skin squamous cell carcinoma", "Perianal skin squamous cell carcinoma", "Perianal Skin Squamous Cell Carcinoma", "Squamous Cell Carcinoma of Anal Margin", "squamous cell carcinoma of anal margin", "Squamous cell carcinoma of anal margin", "Squamous Cell Carcinoma of the Anal Margin", "squamous cell carcinoma of the anal margin", "SCC - Squamous cell carcinoma of anal margin", "Squamous cell carcinoma of anal margin (disorder)", "squamous cell carcinoma of anal margin (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anal margin squamous cell carcinoma", "shortest_name_length": 35}
{"curie": "MONDO:0015381", "names": ["commissural lip fistula", "labial commissure cysts and fistulae of the face and oral cavity", "cysts and fistulae of the face and oral cavity of labial commissure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "commissural lip fistula", "shortest_name_length": 23}
{"curie": "UMLS:C0860514", "names": ["Dreamy state"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dreamy state", "shortest_name_length": 12}
{"curie": "MONDO:0030787", "names": ["SPGF71", "spermatogenic failure 71", "SPERMATOGENIC FAILURE 71"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 71", "shortest_name_length": 6}
{"curie": "MONDO:0009652", "names": ["ML 3C", "ML IIIC", "ML 3 gamma", "ML III gamma", "ML III GAMMA", "mucolipidosis 3C", "MUCOLIPIDOSIS IIIC", "Mucolipidosis IIIC", "GNPTG-mucolipidosis", "mucolipidosis 3 gamma", "mucolipidosis III gamma", "MUCOLIPIDOSIS III GAMMA", "Mucolipidosis III Gamma", "Mucolipidosis type 3 gamma", "mucolipidosis type 3 gamma", "Mucolipidosis Type III Gamma", "mucolipidosis type III gamma", "Mucolipidosis type III gamma", "MUCOLIPIDOSIS III, VARIANT FORM", "Mucolipidosis III, Variant Form", "mucolipidosis III, variant form", "mucolipidosis III, Iranian variant form", "MUCOLIPIDOSIS III, IRANIAN VARIANT FORM", "Mucolipidosis III, Iranian Variant Form", "mucolipidosis III, complementation group C", "Mucolipidosis III, Complementation Group C", "MUCOLIPIDOSIS III, COMPLEMENTATION GROUP C"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "GNPTG-mucolipidosis", "shortest_name_length": 5}
{"curie": "MONDO:0017840", "names": ["classic 21-OHD CAH, simple virilizing form", "classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, simple virilizing form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, simple virilizing form", "shortest_name_length": 42}
{"curie": "MONDO:0006090", "names": ["Appendix Metaplastic Polyp", "appendix metaplastic polyp", "Appendix Hyperplastic Polyp", "appendix hyperplastic polyp", "Hyperplastic polyp of appendix", "vermiform appendix hyperplastic polyp", "Hyperplastic polyp of appendix (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "appendix hyperplastic polyp", "shortest_name_length": 26}
{"curie": "UMLS:C0334044", "names": ["Dyscrasia", "Dysplasia", "dyscrasia", "dysplasia", "DYSPLASIA", "DYSPLASIAS", "dysplasias", "dysplastic", "Dysplastic", "Dysplasias", "dysplasia type", "Dysplasia, NOS", "dysplasia_type", "dysplasia (abnormal growth)", "abnormal structure or growth", "Dysplasia (morphologic abnormality)", "abnormal cellular structure or growth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dysplasia", "shortest_name_length": 9}
{"curie": "UMLS:C4331320", "names": ["Stage IB Mycosis Fungoides", "Stage IB Mycosis Fungoides AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Mycosis Fungoides AJCC v7", "shortest_name_length": 26}
{"curie": "UMLS:C1332544", "names": ["Benzene-Related Acute Myeloid Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benzene-Related Acute Myeloid Leukemia", "shortest_name_length": 38}
{"curie": "MONDO:0016658", "names": ["Del(8)(p23.1)", "8p23.1 deletion", "monosomy 8p23.1", "Monosomy 8p23.1", "Monosomy 8p23 1", "Deletion 8p23 1", "deletion 8p23.1", "chromosome 8p23.1 deletion", "8p23.1 microdeletion syndrome", "Chromosome 8, monosomy 8p23 1", "8p23.1 microdeletion syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "8p23.1 microdeletion syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0004611", "names": ["soft palate cancer", "cancer of soft palate", "malignant soft palate tumor", "Malignant Soft Palate Tumor", "malignant tumor of soft palate", "malignant soft palate neoplasm", "Malignant Tumor of Soft Palate", "Malignant tumor of soft palate", "Malignant Soft Palate Neoplasm", "Malignant tumour of soft palate", "malignant neoplasm of soft palate", "Malignant neoplasm of soft palate", "Malignant Neoplasm of Soft Palate", "malignant tumor of the soft Palate", "malignant tumor of the soft palate", "Malignant Tumor of the Soft Palate", "Malignant Neoplasm of the Soft Palate", "malignant neoplasm of the soft palate", "Malignant tumor of soft palate (disorder)", "malignant neoplasm of soft palate (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "soft palate cancer", "shortest_name_length": 18}
{"curie": "MONDO:0004114", "names": ["SCCB", "small cell bladder cancer", "Small cell bladder cancer", "small cell bladder carcinoma", "Small cell bladder carcinoma", "Bladder Small Cell Carcinoma", "Small cell carcinoma of the bladder", "small cell carcinoma of the bladder", "urinary bladder small cell carcinoma", "small cell carcinoma of urinary bladder", "Bladder Small Cell Neuroendocrine Cancer", "bladder small cell neuroendocrine cancer", "small cell carcinoma of the urinary bladder", "bladder small cell neuroendocrine carcinoma", "Small cell carcinoma of the urinary bladder", "Bladder Small Cell Neuroendocrine Carcinoma", "Small cell neuroendocrine carcinoma of bladder", "urinary bladder small cell neuroendocrine carcinoma", "small cell neuroendocrine carcinoma of urinary bladder", "small cell/neuroendocrine carcinoma of urinary bladder", "Small Cell Neuroendocrine Carcinoma of Urinary Bladder", "Small cell neuroendocrine carcinoma of bladder (disorder)", "Small Cell Neuroendocrine Carcinoma of the Urinary Bladder", "small cell neuroendocrine carcinoma of the urinary bladder", "Poorly differentiated neuroendocrine carcinoma of the bladder", "poorly differentiated neuroendocrine carcinoma of the bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urinary bladder small cell neuroendocrine carcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0015248", "names": ["Fenton-Wilkinson-Toselano syndrome", "ataxia-photosensitivity-short stature syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ataxia-photosensitivity-short stature syndrome", "shortest_name_length": 34}
{"curie": "UMLS:C2984089", "names": ["Rectal Cancer by AJCC v7 Stage", "Rectal Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rectal Cancer by AJCC v7 Stage", "shortest_name_length": 30}
{"curie": "MONDO:0030966", "names": ["NFSRA", "NEUROFACIOSKELETAL SYNDROME WITH OR WITHOUT RENAL AGENESIS", "neurofacioskeletal syndrome with or without renal agenesis", "NEURODEVELOPMENTAL DISORDER WITH CORPUS CALLOSUM AGENESIS, CRANIOFACIAL DYSMORPHISM, AND SKELETAL ANOMALIES, WITH OR WITHOUT RENAL AGENESIS", "Neurodevelopmental Disorder With Corpus Callosum Agenesis, Craniofacial Dysmorphism, and Skeletal Anomalies, With or Without Renal Agenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurofacioskeletal syndrome with or without renal agenesis", "shortest_name_length": 5}
{"curie": "MONDO:0030937", "names": ["MC2DN3", "mitochondrial complex 2 deficiency, nuclear type 3", "mitochondrial complex II deficiency, nuclear type 3", "MITOCHONDRIAL COMPLEX II DEFICIENCY, NUCLEAR TYPE 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 2 deficiency, nuclear type 3", "shortest_name_length": 6}
{"curie": "MONDO:0007717", "names": ["hemoglobin--variants for which the chain carrying the mutation 1S unknown or uncertain", "HEMOGLOBIN--VARIANTS FOR WHICH THE CHAIN CARRYING THE MUTATION IS UNKNOWN OR UNCERTAIN", "HEMOGLOBIN--variants FOR which the chain carrying the mutation IS unknown or uncertain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemoglobin--variants for which the chain carrying the mutation 1S unknown or uncertain", "shortest_name_length": 86}
{"curie": "UMLS:C0279619", "names": ["Adult Acute M6 Leukemia", "adult acute M6 leukemia", "Acute Erythroid Leukemia", "M6 leukemia, adult acute", "Adult Acute Erythroid Leukemia", "leukemia, adult acute erythro-", "adult acute erythroid leukemia (M6)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Acute Erythroid Leukemia", "shortest_name_length": 23}
{"curie": "UMLS:C0948277", "names": ["Hydrometra", "hydrometra", "Hydrouterus", "fluid uterus", "uterus fluid", "fluids uterus", "Fluid in uterus", "fluid in uterus", "Hydrometra (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hydrometra", "shortest_name_length": 10}
{"curie": "UMLS:C2930797", "names": ["Hepatic ductular hypoplasia", "Hepatic Ductular Hypoplasia", "Ductular Hypoplasia, Hepatic", "Hypoplasia, Hepatic Ductular", "Paucity of Interlobular Bile Ducts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatic ductular hypoplasia", "shortest_name_length": 27}
{"curie": "MONDO:0014840", "names": ["AGM8", "AGM8A", "agammaglobulinemia 8A", "TCF3 autosomal agammaglobulinemia", "agammaglobulinemia 8, autosomal dominant", "AGAMMAGLOBULINEMIA 8A, AUTOSOMAL DOMINANT", "agammaglobulinemia 8, autosomal dominant; AGM8", "autosomal agammaglobulinemia caused by mutation in TCF3", "agammaglobulinemia, autosomal dominant, due to TCF3 defect", "AGAMMAGLOBULINEMIA, AUTOSOMAL DOMINANT, DUE TO TCF3 DEFECT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "agammaglobulinemia 8, autosomal dominant", "shortest_name_length": 4}
{"curie": "UMLS:C5667249", "names": ["Recurrent Immunoblastic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Immunoblastic Lymphoma", "shortest_name_length": 32}
{"curie": "UMLS:C0151946", "names": ["lung; thrombosis", "thrombosis; lung", "thrombosis pulmonary", "pulmonary thrombosis", "THROMBOSIS PULMONARY", "Thrombosis;pulmonary", "Pulmonary thrombosis", "Thrombosis pulmonary", "PULMONARY THROMBOSIS", "thrombosis; pulmonary", "pulmonary; thrombosis", "Pulmonary thrombosis NOS", "Pulmonary vessel thrombosis", "Pulmonary thrombosis (disorder)", "Pulmonary thrombosis (diagnosis)", "thrombosis of blood vessel pulmonary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pulmonary thrombosis", "shortest_name_length": 16}
{"curie": "UMLS:C4525895", "names": ["Stage IV Pancreatic Neuroendocrine Tumor", "Stage IV Pancreatic Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Pancreatic Neuroendocrine Tumor AJCC v8", "shortest_name_length": 40}
{"curie": "UMLS:C4684866", "names": ["Refractory Ewing Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Ewing Sarcoma", "shortest_name_length": 24}
{"curie": "UMLS:C3900097", "names": ["Penile Cancer", "Adult Penile Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Penile Carcinoma", "shortest_name_length": 13}
{"curie": "MONDO:0001611", "names": ["Lacrimal sac cellulitis", "phlegmonous dacryocystitis", "Cellulitis of lacrimal sac", "Phlegmonous dacryocystitis", "Phlegmonous dacryocystitis (disorder)", "phlegmonous dacryocystitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phlegmonous dacryocystitis", "shortest_name_length": 23}
{"curie": "UMLS:C3897536", "names": ["Stage IIB Rectal Cancer", "Stage IIB Rectal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Rectal Cancer AJCC v7", "shortest_name_length": 23}
{"curie": "MONDO:0032867", "names": ["PNCA5", "PANCREATIC CANCER, SUSCEPTIBILITY TO, 5", "pancreatic cancer, susceptibility to, 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic cancer, susceptibility to, 5", "shortest_name_length": 5}
{"curie": "MONDO:0002040", "names": ["Mycosis;skin", "skin mycoses", "skin; mycosis", "mycosis; skin", "Dermatomycoses", "DERMATOMYCOSIS", "Dermal mycosis", "Dermatomycosis", "dermatomycosis", "fungus; eczema", "eczema; fungus", "dermal mycosis", "dermatomycoses", "epidermomycosis", "Cutaneous mycosis", "Dermatitis;fungal", "FUNGAL DERMATITIS", "DERMATITIS FUNGAL", "cutaneous mycosis", "Fungal dermatitis", "Dermatitis fungal", "Fungal dermatosis", "fungal dermatitis", "mycosis; cutaneous", "Dermatitis fungoid", "DERMATITIS FUNGOID", "fungus; dermatitis", "cutaneous; mycosis", "dermatitis; fungus", "fungal skin disease", "skin fungal disease", "Dermal mycosis, NOS", "Fungal Skin Diseases", "diseases fungal skin", "skin fungus infection", "fungus infection skin", "Infection;fungus;skin", "skin fungal infection", "fungal skin disorders", "Dermatitis fungal NOS", "SKIN INFECTION FUNGAL", "Fungal dermatitis NOS", "Fungal skin infection", "fungal infection skin", "fungal skin infection", "Skin Diseases, Fungal", "fungal infections skin", "Fungal dermatitis, NOS", "Dermatophyte Infection", "Cutaneous mycosis, NOS", "fungus infections skin", "fungus; infection, skin", "infection; fungus, skin", "infection; mycotic, skin", "skin; infection, mycotic", "mycotic; infection, skin", "Cutaneous fungal disease", "fungal infection of skin", "Fungal infection of skin", "infection; skin, mycotic", "Skin fungal infection NOS", "Fungal infections of skin", "Dermal mycosis (disorder)", "dermatomycosis (diagnosis)", "superficial mycosis dermal", "dermal mycosis (diagnosis)", "Dermatomycosis, unspecified", "infection; skin, due to fungus", "skin; infection, due to fungus", "fungal dermatological conditions", "Dermatomycosis, other and unspecified", "fungal dermatological conditions (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermatomycosis", "shortest_name_length": 12}
{"curie": "UMLS:C4054945", "names": ["FSGS Collapsing Variant", "Focal Segmental Glomerulosclerosis Collapsing Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Focal Segmental Glomerulosclerosis Collapsing Variant", "shortest_name_length": 23}
{"curie": "UMLS:C0854695", "names": ["Silicon granuloma", "Silicon Granuloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Silicon granuloma", "shortest_name_length": 17}
{"curie": "MONDO:0010242", "names": ["Holmes Benacerraf syndrome", "fetal akinesia syndrome X-linked", "Fetal akinesia syndrome X-linked", "Fetal akinesia syndrome, X-linked", "fetal akinesia syndrome, X-linked", "FETAL AKINESIA SYNDROME, X-LINKED", "X-linked form of fetal akinesia syndrome", "fetal akinesia deformation sequence syndrome X-linked", "Brain malformation, growth retardation, hypokinesia and polyhydramnios", "polyhydramnios, hypokinesia, brain malformations, telecanthus, and narrow palpebral fissures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fetal akinesia syndrome, X-linked", "shortest_name_length": 26}
{"curie": "MONDO:0011332", "names": ["DYSERYTHROPOIESIS, CONGENITAL, WITH ULTRASTRUCTURALLY NORMAL ERYTHROBLAST HETEROCHROMATIN", "Dyserythropoiesis, congenital, with ultrastructurally normal erythroblast heterochromatin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dyserythropoiesis, congenital, with ultrastructurally normal erythroblast heterochromatin", "shortest_name_length": 89}
{"curie": "MONDO:0015010", "names": ["atypical NKA", "atypical glycine encephalopathy", "atypical non-ketotic hyperglycinemia", "GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE", "GLYCINE encephalopathy with normal serum GLYCINE", "Glycine encephalopathy with normal serum Glycine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical glycine encephalopathy", "shortest_name_length": 12}
{"curie": "UMLS:C2983695", "names": ["Cervical Cancer by AJCC v6 Stage", "Cervical Carcinoma by AJCC v6 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Cancer by AJCC v6 Stage", "shortest_name_length": 32}
{"curie": "UMLS:C0243057", "names": ["Stomatognathic System Abnormality", "Abnormality, Stomatognathic System", "Stomatognathic System Abnormalities", "Abnormalities, Stomatognathic System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stomatognathic System Abnormalities", "shortest_name_length": 33}
{"curie": "MONDO:0009113", "names": ["ECYT8", "DPGM deficiency", "BPGM DEFICIENCY", "BPGM deficiency", "DPGM DEFICIENCY", "familial erythrocytosis 8", "ERYTHROCYTOSIS, FAMILIAL, 8", "erythrocytosis, familial, 8", "BISPHOSPHOGLYCEROMUTASE DEFICIENCY", "bisphosphoglyceromutase deficiency", "Diphosphoglycerate mutase deficiency", "Bisphosphoglycerate Mutase Deficiency", "Deficiency of glycerate phosphomutase", "BISPHOSPHOGLYCERATE MUTASE DEFICIENCY", "bisphosphoglycerate mutase deficiency", "Deficiency of diphosphoglycerate mutase", "Deficiency of bisphosphoglycerate mutase", "diphosphoglycerate phosphatase deficiency", "Diphosphoglycerate Phosphatase Deficiency", "Deficiency of bisphosphoglycerate synthase", "Deficiency of bisphosphoglycerate mutase (disorder)", "DIPHOSPHOGLYCERATE MUTASE DEFICIENCY OF ERYTHROCYTE", "diphosphoglycerate mutase deficiency of erythrocyte", "hemolytic anemia due to diphosphoglycerate mutase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemolytic anemia due to diphosphoglycerate mutase deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0011952", "names": ["ALS7", "ALS7 (diagnosis)", "Amyotrophic Lateral Sclerosis 7", "AMYOTROPHIC LATERAL SCLEROSIS 7", "amyotrophic lateral sclerosis 7", "amyotrophic lateral sclerosis ALS7", "amyotrophic lateral sclerosis type 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyotrophic lateral sclerosis type 7", "shortest_name_length": 4}
{"curie": "MONDO:0010108", "names": ["TGCT", "MGCT", "seminoma", "teratoma, testicular", "MALE GERM CELL TUMOR", "Male germ cell tumor", "testis germ cell tumor", "endodermal sinus tumor", "spermatocytic seminoma", "EMBRYONAL CELL CARCINOMA", "embryonal cell carcinoma", "germ cell tumors, somatic", "testicular tumor, somatic", "germ cell tumor of testis", "Germ Cell Tumor of Testis", "Germ cell tumor of testis", "Germ cell tumour of testis", "Testicular germ cell tumor", "testicular germ cell tumor", "TESTICULAR GERM CELL TUMOR", "Testicular Germ Cell Tumor", "Testicular germ cell tumour", "testicular germ cell cancer", "germ cell neoplasm of testis", "Germ Cell Neoplasm of Testis", "Testicular Germ Cell Neoplasm", "Germ Cell Tumor of the Testis", "germ cell tumor of the testis", "testicular germ cell neoplasm", "male germ cell tumor, somatic", "testicular germ cell neoplasms", "Testicular Germ Cell Neoplasms", "spermatocytic seminoma, somatic", "Germ Cell Neoplasm of the Testis", "germ cell neoplasm of the testis", "nonseminomatous germ cell tumors", "Germ cell tumor of testis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular germ cell tumor", "shortest_name_length": 4}
{"curie": "UMLS:C0473390", "names": ["Threatened Preterm Labor", "LABOR PRETERM THREATENED", "Threatened premature labor", "Threatened Premature Labor", "threatened premature labor", "Threatened premature labour", "threatened premature labor (diagnosis)", "Premature labor after 22 weeks but before 37 completed weeks of gestation without delivery", "Premature labour after 22 weeks but before 37 completed weeks of gestation without delivery", "Premature labor after 22 weeks, but before 37 completed weeks of gestation without delivery"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Threatened premature labor", "shortest_name_length": 24}
{"curie": "MONDO:0003764", "names": ["pediatric meningeal melanoma", "childhood meningeal melanoma", "Pediatric Meningeal Melanoma", "Childhood Meningeal Melanoma", "childhood leptomeningeal melanoma", "pediatric leptomeningeal melanoma", "Pediatric Leptomeningeal Melanoma", "Childhood Leptomeningeal Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pediatric leptomeningeal melanoma", "shortest_name_length": 28}
{"curie": "MONDO:0011800", "names": ["GLM4", "glioma susceptibility 4", "GLIOMA SUSCEPTIBILITY 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glioma susceptibility 4", "shortest_name_length": 4}
{"curie": "MONDO:0006276", "names": ["Myofibroblastic tumor, peribronchial", "inflammatory myofibroblastic lung tumor", "lung inflammatory myofibroblastic tumor", "Lung Inflammatory Myofibroblastic Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung inflammatory myofibroblastic tumor", "shortest_name_length": 36}
{"curie": "MONDO:0013268", "names": ["FND2", "ALX4-related FNDAG", "FRONTONASAL DYSPLASIA 2", "frontonasal dysplasia 2", "Frontonasal dysplasia type 2", "frontonasal dysplasia type 2", "frontonasal dysplasia with alopecia and genital anomaly", "Frontonasal dysplasia-alopecia-genital anomalies syndrome", "Craniofrontonasal dysplasia with alopecia and hypogonadism", "frontonasal dysplasia with alopecia and genital abnomality", "Frontonasal dysplasia with alopecia and genital abnomality", "craniofrontonasal dysplasia with alopecia and hypogonadism", "Frontonasal dysplasia with alopecia and genital anomaly syndrome", "Frontonasal dysplasia with alopecia and genital anomaly syndrome (disorder)", "ALX4 (human aristaless-like 4) related frontonasal dysplasia with alopecia and genital anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontonasal dysplasia with alopecia and genital anomaly", "shortest_name_length": 4}
{"curie": "MONDO:0018535", "names": ["biliary cystadenocarcinoma", "intrahepatic bile duct cystadenocarcinoma", "Intrahepatic Bile Duct Cystadenocarcinoma", "cystadenocarcinoma of intrahepatic bile duct", "cystadenocarcinoma of intrahepatic bile duct (diagnosis)", "Intrahepatic Bile Duct MCN with an Associated Invasive Carcinoma", "Intrahepatic Bile Duct Mucinous Cystic Neoplasm with an Associated Invasive Cancer", "Intrahepatic Bile Duct Mucinous Cystic Neoplasm with an Associated Invasive Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "biliary cystadenocarcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0000670", "names": ["Auditory agnosia", "auditory agnosia", "Agnosia Auditory", "Auditory Agnosia", "Acoustic agnosia", "Auditory Agnosias", "Cortical deafness", "Agnosia, acoustic", "Cortical Deafness", "Agnosia, Auditory", "Agnosia, auditory", "cortical deafness", "Deafness, Cortical", "Agnosias, Auditory", "Auditory agnosia (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cortical deafness", "shortest_name_length": 16}
{"curie": "UMLS:C4054399", "names": ["Nephrotic Syndrome - ANLN Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - ANLN Associated", "shortest_name_length": 36}
{"curie": "MONDO:0010053", "names": ["HS3", "SPH3", "spherocytosis, type 3", "SPHEROCYTOSIS, TYPE 3", "Spherocytosis, Type 3", "hereditary spherocytosis 3", "SPHEROCYTOSIS, HEREDITARY, 3", "spherocytosis, hereditary, 3", "Spherocytosis, Hereditary, 3", "SPTA1 hereditary spherocytosis", "hereditary spherocytosis type 3", "SPHEROCYTOSIS, TYPE 3 (disorder)", "hereditary spherocytosis caused by mutation in SPTA1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spherocytosis type 3", "shortest_name_length": 3}
{"curie": "UMLS:C0749794", "names": ["Upper Limb Deformities, Congenital", "Congenital deformity of upper limb", "congenital deformity of upper limb", "UPPER EXTREMITY DEFORMITY CONGENITAL", "congenital deformity of an upper limb", "Upper Extremity Deformities, Congenital", "Congenital deformity of upper limb (disorder)", "congenital deformity of upper limb (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Upper Extremity Deformities, Congenital", "shortest_name_length": 34}
{"curie": "MONDO:0001282", "names": ["Endosalpingosis", "fallopian tube endometriosis", "Fallopian Tube Endometriosis", "fallopian tube; endometriosis", "endometriosis; fallopian tube", "Adenomyosis of fallopian tube", "endometriosis of fallopian tube", "Endometriosis of fallopian tube", "Endometriosis fallopian tube NOS", "fallopian tube endometriosis (disease)", "endometriosis (disease) of fallopian tube", "Endometriosis of fallopian tube (disorder)", "endometriosis of fallopian tube (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fallopian tube endometriosis", "shortest_name_length": 15}
{"curie": "MONDO:0035945", "names": ["B-lymphoblastic leukemia/lymphoma with t(5;14)(q31.1;q32.3)", "B-Lymphoblastic Leukemia/Lymphoma with t(5;14)(q31;q32); IL3-IGH", "B lymphoblastic leukemia/lymphoma with t(5;14)(q31;q32); IL3-IGH", "B Lymphoblastic Leukemia/Lymphoma with t(5;14)(q31;q32); IL3-IGH", "B lymphoblastic leukemia lymphoma with t(5;14)(q31;q32); IL3-IGH", "B lymphoblastic leukemia lymphoma with t(5;14) (q31;q32); IL3-IGH", "B lymphoblastic leukaemia lymphoma with t(5;14)(q31;q32); IL3-IGH", "B Lymphoblastic Leukemia/Lymphoma with t(5;14)(q31.1;q32.3); IL3-IGH", "B lymphoblastic leukemia lymphoma with t(5;14)(q31;q32); IL3-IGH (disorder)", "B lymphoblastic leukemia lymphoma with t(5;14) (q31;q32); IL3-IGH (diagnosis)", "B lymphoblastic leukemia lymphoma with t(5;14)(q31;q32); IL3-IGH (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-lymphoblastic leukemia/lymphoma with t(5;14)(q31.1;q32.3)", "shortest_name_length": 59}
{"curie": "UMLS:C1332509", "names": ["Benign Intracranial Tumor", "Benign Intracranial Neoplasm", "Intracranial Neoplasms, Benign"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Intracranial Neoplasm", "shortest_name_length": 25}
{"curie": "UMLS:C4055193", "names": ["Congenital FSGS", "Congenital Nephrotic Syndrome - Focal Segmental Glomerulosclerosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Nephrotic Syndrome - Focal Segmental Glomerulosclerosis", "shortest_name_length": 15}
{"curie": "MONDO:0009246", "names": ["Friedreich ataxia congenital glaucoma", "Congenital glaucoma and Friedreich ataxia", "FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA", "Friedreich Ataxia and Congenital Glaucoma", "Friedreich ataxia and congenital glaucoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Friedreich ataxia and congenital glaucoma", "shortest_name_length": 37}
{"curie": "UMLS:C3495797", "names": ["Peripheral artery stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peripheral artery stenosis", "shortest_name_length": 26}
{"curie": "MONDO:0006429", "names": ["Spleen", "splenic hodgkin lymphoma", "Splenic Hodgkin Lymphoma", "Splenic Hodgkins Lymphoma", "Splenic Hodgkin's Disease", "splenic Hodgkin's disease", "splenic Hodgkins lymphoma", "Hodgkin disease of spleen", "Hodgkin lymphoma of spleen", "Splenic Hodgkin's Lymphoma", "splenic Hodgkin's lymphoma", "Hodgkin's disease of spleen", "Hodgkin's Disease of Spleen", "Hodgkin's Lymphoma of Spleen", "Hodgkin's lymphoma of spleen", "Hodgkin's Disease of the Spleen", "Hodgkin's disease of the spleen", "Hodgkin's disease, NOS of spleen", "Hodgkin's lymphoma of the spleen", "Hodgkin's Lymphoma of the Spleen", "primary splenic Hodgkin's lymphoma", "Primary Splenic Hodgkin's Lymphoma", "Hodgkin lymphoma of spleen (diagnosis)", "Hodgkin's disease of spleen (disorder)", "Hodgkin's lymphoma of spleen (diagnosis)", "Hodgkin's disease, unspecified type, spleen", "Hodgkin's disease, unspecified type, involving spleen"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "splenic hodgkin lymphoma", "shortest_name_length": 6}
{"curie": "UMLS:C0948357", "names": ["infection urethra", "infection; urethra", "Urethral infection", "Urethral Infection", "urethra; infection", "Urethral infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urethral Infection", "shortest_name_length": 17}
{"curie": "MONDO:0011148", "names": ["Spondylospinal Thoracic Dysostosis", "spondylospinal thoracic dysostosis", "SPONDYLOSPINAL THORACIC DYSOSTOSIS", "Spondylospinal thoracic dysostosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spondylospinal thoracic dysostosis", "shortest_name_length": 34}
{"curie": "MONDO:0043975", "names": ["Dysreflexia", "dysreflexia", "Autonomic dysreflexia", "autonomic dysreflexia", "AUTONOMIC DYSREFLEXIA", "Autonomic Dysreflexia", "Dysreflexia, autonomic", "Autonomic Dysreflexias", "Dysreflexia, Autonomic", "autonomic Dysreflexias", "Autonomic Hyperreflexia", "autonomic hyperreflexia", "Dysreflexias, autonomic", "AUTONOMIC HYPERREFLEXIA", "Dysreflexias, Autonomic", "Hyperreflexia, Autonomic", "Autonomic Hyperreflexias", "hyperreflexia, autonomic", "autonomic Hyperreflexias", "hyperreflexias, autonomic", "Hyperreflexias, Autonomic", "RNDx autonomic dysreflexia", "Spinal Autonomic Dysreflexia", "spinal autonomic Dysreflexia", "Dysreflexia, spinal autonomic", "Dysreflexia, Spinal Autonomic", "Autonomic Dysreflexia, Spinal", "Spinal Autonomic Dysreflexias", "spinal autonomic Dysreflexias", "autonomic Dysreflexia, spinal", "autonomic Dysreflexias, spinal", "Dysreflexias, Spinal Autonomic", "Autonomic Dysreflexias, Spinal", "Dysreflexias, spinal autonomic", "Autonomic dysreflexia (disorder)", "autonomic dysreflexia (diagnosis)", "RNDx autonomic dysreflexia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autonomic dysreflexia", "shortest_name_length": 11}
{"curie": "MONDO:0008151", "names": ["GDD", "Levin syndrome 2", "gnathodiaphyseal sclerosis", "Gnathodiaphyseal Sclerosis", "Gnathodiaphyseal sclerosis", "GNATHODIAPHYSEAL dysplasia", "Gnathodiaphyseal dysplasia", "GNATHODIAPHYSEAL SCLEROSIS", "GNATHODIAPHYSEAL DYSPLASIA", "Gnathodiaphyseal Dysplasia", "gnathodiaphyseal dysplasia", "osteogenesis imperfecta Levin type", "osteogenesis imperfecta, Levin type", "Osteogenesis imperfecta, Levin type", "Gnathodiaphyseal dysplasia syndrome", "Gnathodiaphyseal dysplasia syndrome (disorder)", "OSTEOGENESIS IMPERFECTA WITH UNUSUAL SKELETAL LESIONS", "Osteogenesis imperfecta with unusual skeletal lesions", "osteogenesis imperfecta with unusual skeletal lesions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gnathodiaphyseal dysplasia", "shortest_name_length": 3}
{"curie": "MONDO:0007912", "names": ["LITHIUM TRANSPORT", "lithium transport"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lithium transport", "shortest_name_length": 17}
{"curie": "MONDO:0019740", "names": ["TTP", "iTTP", "aTTP", "acquired TTP", "Acquired TTP", "Moschowitz syndrome", "acquired ADAMTS13 deficiency", "Acquired ADAMTS13 Deficiency", "purpura, thrombotic thrombocytopenic", "Acquired Thrombotic Thrombocytopenic Purpura", "acquired thrombotic thrombocytopenic purpura", "Acquired thrombotic thrombocytopenic purpura", "Thrombotic thrombocytopenic purpura, acquired", "Idiopathic thrombotic thrombocytopenic purpura", "idiopathic thrombotic thrombocytopenic purpura", "IDIOPATHIC THROMBOTIC THROMBOCYTOPENIC PURPURA", "autoimmune thrombotic thrombocytopenic purpura", "Autoimmune thrombotic thrombocytopenic purpura", "Acquired thrombotic thrombocytopenic purpura (TTP)", "Immune-mediated thrombotic thrombocytopenic purpura", "Autoimmune thrombotic thrombocytopenic purpura (TTP)", "Acquired thrombotic thrombocytopenic purpura (disorder)", "Autoimmune thrombotic thrombocytopenic purpura (disorder)", "Thrombotic thrombocytopenic purpura due to anti-ADAMTS-13 antibodies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired thrombotic thrombocytopenic purpura", "shortest_name_length": 3}
{"curie": "MONDO:0033566", "names": ["COXPD48", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 48", "combined oxidative phosphorylation deficiency 48"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation deficiency 48", "shortest_name_length": 7}
{"curie": "MONDO:0008216", "names": ["pelvic lipomatosis with crossed renal ectopia", "Pelvic Lipomatosis with Crossed Renal Ectopia", "PELVIC LIPOMATOSIS WITH CROSSED RENAL ECTOPIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pelvic lipomatosis with crossed renal ectopia", "shortest_name_length": 45}
{"curie": "UMLS:C5446579", "names": ["Metastatic Distal Bile Duct Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Distal Bile Duct Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0000488", "names": ["periampullary adenoma", "periampullary region of duodenum adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "periampullary adenoma", "shortest_name_length": 21}
{"curie": "MONDO:0022496", "names": ["Van Bervliet syndrome", "arthrogryposis IUGR thoracic dystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis IUGR thoracic dystrophy", "shortest_name_length": 21}
{"curie": "UMLS:C5420253", "names": ["Relapsed Ganglioneuroblastoma", "Recurrent Ganglioneuroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Ganglioneuroblastoma", "shortest_name_length": 29}
{"curie": "MONDO:0005001", "names": ["GASTRITIS CHRONIC", "Chronic Gastritis", "Gastritis chronic", "Chronic gastritis", "chronic gastritis", "gastritis chronic", "chronic; gastritis", "gastritis; chronic", "GASTRITIS, CHRONIC", "CG - Chronic gastritis", "Chronic gastritis, NOS", "chronic gastritis (disease)", "Chronic gastritis (disorder)", "gastritis (disease), chronic", "Chronic gastritis (diagnosis)", "Unspecified chronic gastritis", "Chronic gastritis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic gastritis", "shortest_name_length": 17}
{"curie": "UMLS:C1333110", "names": ["Colorectal High-Grade Dysplasia", "Large Intestinal High Grade Dysplasia", "Colorectal High Grade Intraepithelial Neoplasia", "Colorectal High-Grade Intraepithelial Neoplasia", "Large Intestinal High Grade Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal High Grade Intraepithelial Neoplasia", "shortest_name_length": 31}
{"curie": "UMLS:C1827434", "names": ["Stage I Seminoma", "Stage I Seminoma of Testis", "Stage I Testicular Seminoma", "Seminoma of testis, stage 1", "Stage I Seminoma of the Testis", "Stage I Testicular Seminoma AJCC v7", "Stage I Testicular Seminoma AJCC v6", "Seminoma of testis, stage 1 (disorder)", "Stage I Testicular Seminoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Seminoma of testis, stage 1", "shortest_name_length": 16}
{"curie": "MONDO:0001588", "names": ["chronic lacrimal gland enlargement", "Chronic lacrimal gland enlargement", "chronic enlargement of lacrimal gland", "Chronic enlargement of lacrimal gland", "Chronic enlargement of lacrimal gland (disorder)", "chronic enlargement of lacrimal gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic lacrimal gland enlargement", "shortest_name_length": 34}
{"curie": "UMLS:C0684320", "names": ["Regression", "Regressing", "regression", "regressions", "Disease regression", "regression disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disease regression", "shortest_name_length": 10}
{"curie": "UMLS:C1516432", "names": ["Cervical Soft Tissue Tumor", "Cervical Soft Tissue Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Soft Tissue Neoplasm", "shortest_name_length": 26}
{"curie": "UMLS:C1336704", "names": ["CNS Teratoma with Malignant Transformation", "Teratoma of CNS with Malignant Transformation", "Teratoma of the CNS with Malignant Transformation", "Central Nervous System Teratoma with Malignant Transformation", "Teratoma of Central Nervous System with Malignant Transformation", "Teratoma of the Central Nervous System with Malignant Transformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Teratoma with Malignant Transformation", "shortest_name_length": 42}
{"curie": "UMLS:C0043241", "names": ["septic wound", "Septic wound", "infected wound", "Infected wound", "wound infected", "Wound infected", "Wound Infection", "wound infection", "infected wounds", "WOUND INFECTION", "Infection;wound", "Wound infection", "Wound, infected", "Infection, Wound", "Wound Infections", "infection; wound", "wound infections", "wound; infection", "Infections, Wound", "Infected wound, NOS", "Local infection of wound", "wound infection (diagnosis)", "Local infection of wound, NOS", "Local infection of wound (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wound Infection", "shortest_name_length": 12}
{"curie": "MONDO:0013621", "names": ["NPHS5", "nephrotic syndrome type 5", "LAMB2-related infantile-onset nephrotic syndrome", "nephrotic syndrome type 5, with or without ocular abnormalities", "NEPHROTIC SYNDROME, TYPE 5, WITH OR WITHOUT OCULAR ABNORMALITIES", "nephrotic syndrome, type 5, with or without ocular abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "LAMB2-related infantile-onset nephrotic syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0236811", "names": ["Chronobiology Disorder", "Chronobiology Disorders", "Biological Clock Disturbance", "Biological Clock Disturbances", "Disturbance, Biological Clock", "Disturbances, Biological Clock"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronobiology Disorders", "shortest_name_length": 22}
{"curie": "UMLS:C4725618", "names": ["Refractory Endometrial Endometrioid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Endometrial Endometrioid Adenocarcinoma", "shortest_name_length": 50}
{"curie": "MONDO:0015286", "names": ["CDG", "Congenital Disorder of Glycosylation", "Congenital disorder of glycosylation", "congenital disorder of glycosylation", "Congenital Disorders of Glycosylation", "congenital disorders of glycosylation", "carbohydrate-deficient glycoprotein syndrome", "carbohydrate deficient glycoprotein syndrome", "Carbohydrate Deficient Glycoprotein Syndrome", "Carbohydrate deficient glycoprotein syndrome", "Carbohydrate-deficient glycoprotein syndrome", "Carbohydrate-Deficient Glycoprotein Syndrome", "congenital disorder of glycosylation syndrome", "Syndrome, Carbohydrate-Deficient Glycoprotein", "Carbohydrate deficiency glycoprotein syndrome", "Glycoprotein Syndrome, Carbohydrate-Deficient", "Carbohydrate-Deficient Glycoprotein Syndromes", "carbohydrate-deficient glycoprotein syndromes", "Syndromes, Carbohydrate-Deficient Glycoprotein", "CDG - Carbohydrate-deficient glycoprotein syndrome", "Carbohydrate-deficient glycoprotein syndrome (disorder)", "congenital disorder of glycosylation syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital disorder of glycosylation", "shortest_name_length": 3}
{"curie": "MONDO:0004673", "names": ["lower lip cancer", "cancer of lower lip", "malignant lower lip neoplasm", "malignant neoplasm of lower lip", "Malignant neoplasm of external lower lip", "lip neoplasm malignant lower, lipstick area", "Malignant tumor of lipstick area of lower lip", "malignant neoplasm of lower lip, lipstick area", "Malignant tumour of lipstick area of lower lip", "Malignant neoplasm of lower lip, lipstick area", "Malignant neoplasm of lipstick area of lower lip", "Malignant tumor of vermilion border of lower lip", "Malignant tumour of vermilion border of lower lip", "Malignant neoplasm of lower lip, vermilion border", "Malignant neoplasm of vermilion border of lower lip", "malignant neoplasm of vermilion border of lower lip", "lip neoplasm malignant vermilion border of lower lip", "malignant neoplasm of lower lip, lipstick area (diagnosis)", "Malignant tumor of vermilion border of lower lip (disorder)", "malignant neoplasm of vermilion border of lower lip (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lower lip cancer", "shortest_name_length": 16}
{"curie": "UMLS:C0859229", "names": ["Migration of implant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Migration of implant", "shortest_name_length": 20}
{"curie": "UMLS:C4521736", "names": ["Stage IVA Esophageal Squamous Cell Cancer", "Postneoadjuvant Therapy Stage IVA Esophageal Squamous Cell Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postneoadjuvant Therapy Stage IVA Esophageal Squamous Cell Carcinoma AJCC v8", "shortest_name_length": 41}
{"curie": "UMLS:C5238404", "names": ["Refractory Prostate Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Prostate Carcinoma", "shortest_name_length": 29}
{"curie": "UMLS:C3179502", "names": ["Verrucous Epidermal Nevus", "Epidermal Nevus, Verrucous", "Nevus, Verrucous Epidermal", "Linear Verrucous Epidermal Nevus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Linear Verrucous Epidermal Nevus", "shortest_name_length": 25}
{"curie": "MONDO:0008693", "names": ["AMS", "ablepharon macrostomia syndrome", "Ablepharon macrostomia syndrome", "Ablepharon-Macrostomia Syndrome", "ablepharon-macrostomia syndrome", "ABLEPHARON-MACROSTOMIA SYNDROME", "Ablepharon macrostomia syndrome (disorder)", "congenital ablepharon, absent eyelashes/eyebrows, macrostomia, auricular, nasal, genital and other systemic anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ablepharon macrostomia syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0030717", "names": ["IMD97", "IMMUNODEFICIENCY 97 WITH AUTOINFLAMMATION", "immunodeficiency 97 with autoinflammation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 97 with autoinflammation", "shortest_name_length": 5}
{"curie": "UMLS:C0595938", "names": ["EFFECT INCREASED", "effect increased", "INCREASED EFFECT", "effects increased", "effects increasing"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "effect increased", "shortest_name_length": 16}
{"curie": "DOID:0080704", "names": ["Medulloblastoma, SHH-Activated, TP53-Mutant", "medulloblastoma SHH activated and TP53 mutant", "Medulloblastoma, SHH-activated and TP53-mutant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "medulloblastoma SHH activated and TP53 mutant", "shortest_name_length": 43}
{"curie": "UMLS:C0750827", "names": ["hemolytic anemia due to dic", "hemolytic anemia due to disseminated intravascular coagulation", "Hemolytic Anemia due to Disseminated Intravascular Coagulation", "Hemolytic anemia due to disseminated intravascular coagulation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemolytic anemia due to disseminated intravascular coagulation", "shortest_name_length": 27}
{"curie": "MONDO:0005003", "names": ["Chronic Pancreatitis", "PANCREATITIS CHRONIC", "pancreatitis chronic", "Pancreatitis;chronic", "chronic pancreatitis", "Pancreatitis chronic", "Chronic pancreatitis", "pancreatitis, chronic", "PANCREATITIS, CHRONIC", "chronic; pancreatitis", "Pancreatitis, Chronic", "pancreatitis; chronic", "PANCREATITIS RELAPSING", "Relapsing pancreatitis", "Recurrent pancreatitis", "recurrent pancreatitis", "Chronic pancreatitis NOS", "CP - Chronic pancreatitis", "Chronic pancreatitis, NOS", "Chronic pancreas inflammation", "Relapsing chronic pancreatitis", "PANCREATITIS CHRONIC RELAPSING", "chronic relapsing pancreatitis", "Chronic pancreatitis (disorder)", "chronic; pancreatitis, relapsing", "chronic pancreatitis (diagnosis)", "pancreatitis; chronic, relapsing", "Chronic pancreatitis in remission", "pancreatitis; recrudescent [Brill-Zinsser]", "recrudescent [Brill-Zinsser]; pancreatitis", "chronic relapsing pancreatitis (diagnosis)", "Chronic pancreatitis as main diagnosis for the pancreas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic pancreatitis", "shortest_name_length": 20}
{"curie": "UMLS:C1708668", "names": ["Leaflet Disruption Due To Host Tissue Overgrowth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leaflet Disruption Due To Host Tissue Overgrowth", "shortest_name_length": 48}
{"curie": "MONDO:0006990", "names": ["suppurative uveitis", "Suppurative Uveitis", "Uveitis, Suppurative", "Suppurative Uveitides", "Uveitides, Suppurative"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "suppurative uveitis", "shortest_name_length": 19}
{"curie": "UMLS:C4521814", "names": ["Stage IIIC Appendix Cancer", "Stage IIIC Appendix Carcinoma AJCC v8", "Stage IIIC Appendiceal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Appendix Carcinoma AJCC v8", "shortest_name_length": 26}
{"curie": "MONDO:0011669", "names": ["HCS", "hypotonia-cystinuria syndrome", "Hypotonia-cystinuria syndrome", "HYPOTONIA-CYSTINURIA SYNDROME", "Hypotonia cystinuria syndrome", "Hypotonia-Cystinuria Syndrome", "Homozygous 2p21 Deletion Syndrome", "homozygous 2P21 deletion syndrome", "HOMOZYGOUS 2p21 DELETION SYNDROME", "homozygous 2P16 deletion syndrome", "hypotonia-cystinuria syndrome type 1", "hypotonia-cystinuria type 1 syndrome", "cystinuria with mitochondrial disease", "Cystinuria with Mitochondrial Disease", "CYSTINURIA WITH MITOCHONDRIAL DISEASE", "Hypotonia cystinuria syndrome (disorder)", "homozygous 2P16 deletion syndrome, formerly", "HOMOZYGOUS 2p16 DELETION SYNDROME, FORMERLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotonia-cystinuria syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0009898", "names": ["polysaccharide, storage of unusual", "POLYSACCHARIDE, STORAGE OF UNUSUAL", "Polysaccharide, Storage of Unusual"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polysaccharide, storage of unusual", "shortest_name_length": 34}
{"curie": "MONDO:0100325", "names": ["ODCD", "ODCD1", "Goldblatt syndrome", "GOLDBLATT SYNDROME", "odontochondrodysplasia", "Odontochondrodysplasia", "ODONTOCHONDRODYSPLASIA 1", "odontochondrodysplasia 1", "Goldblatt chondrodysplasia", "SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA", "spondylometaphyseal dysplasia with dentinogenesis imperfecta", "Spondylometaphyseal dysplasia with dentinogenesis imperfecta", "chondrodysplasia-dentinogenesis imperfecta-joint laxity syndrome", "Chondrodysplasia-dentinogenesis imperfecta-joint laxity syndrome", "Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome", "Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "odontochondrodysplasia 1", "shortest_name_length": 4}
{"curie": "UMLS:C0578455", "names": ["Abscess limb", "Abscess of limb", "Abscess of limb (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abscess of limb", "shortest_name_length": 12}
{"curie": "MONDO:0006779", "names": ["aneurysm heart", "Mural aneurysm", "Heart Aneurysm", "heart aneurysm", "aneurysm; heart", "Aneurysm, mural", "aneurysm; mural", "heart aneurysms", "heart; aneurysm", "mural; aneurysm", "Aneurysm, Heart", "Heart Aneurysms", "cardiac aneurysm", "Aneurysms, Heart", "Cardiac Aneurysm", "Cardiac aneurysm", "CARDIAC ANEURYSM", "Aneurysm;cardiac", "aneurysm; cardiac", "cardiac aneurysms", "aneurysm of heart", "ANEURYSM, CARDIAC", "Aneurysm of heart", "Aneurysm, Cardiac", "cardiac; aneurysm", "Cardiac Aneurysms", "Aneurysms, Cardiac", "Aneurysm of heart, NOS", "Aneurysm of heart wall", "aneurysm of heart wall", "Mural aneurysm of heart", "Aneurysm of heart (wall)", "Aneurysm of heart (disorder)", "Mural cardiac aneurysm (disorder)", "aneurysm of heart wall (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heart aneurysm", "shortest_name_length": 14}
{"curie": "UMLS:C1333840", "names": ["Grade 2 Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade 2 Malignant Neoplasm", "shortest_name_length": 26}
{"curie": "MONDO:0800089", "names": ["primary bone dysplasia with disorganized development of skeletal components", "primary osteodysplasia with disorganized development of skeletal components", "primary skeletal dysplasia with disorganized development of skeletal components"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary bone dysplasia with disorganized development of skeletal components", "shortest_name_length": 75}
{"curie": "UMLS:C1335002", "names": ["Non-Neoplastic Conjunctival Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Conjunctival Disorder", "shortest_name_length": 36}
{"curie": "MONDO:0003276", "names": ["middle ear disease", "Middle ear problem", "middle ear problem", "Middle Ear Disorder", "ear middle problems", "middle ear disorder", "Middle ear disorder", "middle Ear disorder", "middle ear disorders", "Tubotympanic disease", "disease of middle ear", "disorder of middle ear", "Disorder of middle ear", "Middle ear disorder NOS", "disorders of middle ear", "Tubotympanic disease, NOS", "DISORDERS OF THE MIDDLE EAR", "Disorder of middle ear, NOS", "Middle ear problem (finding)", "middle ear disease or disorder", "Disease or syndrome of middle ear", "disease (or disorder); middle ear", "disease or disorder of middle ear", "Disorder of middle ear (disorder)", "disorders of middle ear (diagnosis)", "DISORDERS OF THE MIDDLE EAR AND EUSTACHIAN TUBE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "middle ear disorder", "shortest_name_length": 18}
{"curie": "MONDO:0024346", "names": ["Tinea amiantacea", "tinea amiantacea", "tinea; amiantacea", "amiantacea; tinea", "Pityriasis amiantacea", "pityriasis amiantacea", "Pityriasis amiantacea (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pityriasis amiantacea", "shortest_name_length": 16}
{"curie": "UMLS:C0520540", "names": ["Hypertension rebound", "rebound hypertension", "Rebound hypertension", "Rebound hypertension (disorder)", "rebound hypertension (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rebound hypertension", "shortest_name_length": 20}
{"curie": "UMLS:C0752203", "names": ["primary dystonia", "Primary Dystonia", "dystonia primary", "Dystonia, Primary", "Primary Dystonias", "Dystonias, Primary", "primary dystonia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dystonia, Primary", "shortest_name_length": 16}
{"curie": "UMLS:C4683743", "names": ["Stage IIA Mycosis Fungoides and Sezary Syndrome AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Mycosis Fungoides and Sezary Syndrome AJCC v8", "shortest_name_length": 55}
{"curie": "MONDO:0012790", "names": ["ALS10", "ALS10 (diagnosis)", "FTLD-TDP, TARDBP-RELATED", "Ftld-TDP, Tardbp-related", "amyotrophic lateral sclerosis 10", "Amyotrophic Lateral Sclerosis 10", "amyotrophic lateral sclerosis ALS10", "TARDBP amyotrophic lateral sclerosis", "amyotrophic lateral sclerosis type 10", "AMYOTROPHIC LATERAL SCLEROSIS 10 (disorder)", "frontotemporal lobar degeneration, TARDBP-related", "amyotrophic lateral sclerosis 10, with or without FTD", "amyotrophic lateral sclerosis caused by mutation in TARDBP", "FRONTOTEMPORAL DEMENTIA WITH TDP43 INCLUSIONS, TARDBP-RELATED", "frontotemporal dementia with Tdp43 inclusions, Tardbp-related", "TARDBP-related frontotemporal lobar degeneration with TDP43 inclusions", "TARDBP-related frontotemporal lobar degeneration with Tdp43 inclusions", "FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, TARDBP-RELATED", "frontotemporal lobar Degeneration with Tdp43 inclusions, Tardbp-related", "AMYOTROPHIC LATERAL SCLEROSIS 10 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA", "amyotrophic lateral sclerosis 10 with or without frontotemporal dementia", "Amyotrophic Lateral Sclerosis 10, With or Without Frontotemporal Dementia", "amyotrophic lateral sclerosis 10, with or without frontotemporal dementia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyotrophic lateral sclerosis type 10", "shortest_name_length": 5}
{"curie": "UMLS:C4683595", "names": ["Lugano Classification Limited Stage Childhood Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Limited Stage Childhood Hodgkin Lymphoma AJCC v8", "shortest_name_length": 70}
{"curie": "MONDO:0000313", "names": ["hypophosphatemia", "HYPOPHOSPHATEMIA", "Hypophosphoremia", "Hypophosphatemia", "Hypophosphataemia", "Hypophosphatemias", "hypophosphataemia", "HYPOPHOSPHATAEMIA", "Hypophosphatemia, NOS", "Hypophosphataemia, NOS", "Low blood phosphate level", "disorder hypophosphatemia", "Serum phosphate decreased", "SERUM PHOSPHATE DECREASED", "Phosphate Serum Decreased", "SERUM PHOSPHORUS DECREASED", "hypophosphatemia (disease)", "Decreased serum phosphorus", "Decrease in serum phosphate", "Hypophosphatemia (disorder)", "Decrease in serum phosphorus", "hypophosphatemia (diagnosis)", "Disorder characterized by hypophosphatemia", "Serum phosphate concentration below normal", "Serum phosphate concentration decreased below normal", "Serum phosphate concentration below normal (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypophosphatemia", "shortest_name_length": 16}
{"curie": "MONDO:0011184", "names": ["DVD", "CAS", "das", "SPCH1", "Pure CAS", "Isolated CAS", "articulatory apraxia", "Speech Language Disorder 1", "speech-language disorder 1", "SPEECH-LANGUAGE DISORDER 1", "speech-language disorder-1", "Speech-Language Disorder 1", "Speech-Language Disorder 1s", "CHILDHOOD APRAXIA OF SPEECH", "childhood apraxia of speech", "Childhood apraxia of speech", "Disorder 1, Speech-Language", "developmental verbal apraxia", "Developmental Verbal Apraxia", "1s, Speech-Language Disorder", "Disorder 1s, Speech-Language", "Apraxia, Developmental Verbal", "Developmental Verbal Apraxias", "Verbal Apraxia, Developmental", "Developmental Verbal Dyspraxia", "Apraxias, Developmental Verbal", "Developmental verbal dyspraxia", "Verbal Apraxias, Developmental", "DEVELOPMENTAL VERBAL DYSPRAXIA", "developmental verbal dyspraxia", "speech-language disorder type 1", "Developmental Verbal Dyspraxias", "developmental apraxia of speech", "Verbal Dyspraxia, Developmental", "Speech-language disorder type 1", "Dyspraxia, Developmental Verbal", "Dyspraxias, Developmental Verbal", "Pure childhood apraxia of speech", "Verbal Dyspraxias, Developmental", "DVD - Developmental verbal apraxia", "Isolated childhood apraxia of speech", "Isolated developmental verbal dyspraxia", "Developmental verbal dyspraxia (disorder)", "Developmental verbal dyspraxia (diagnosis)", "SPEECH AND LANGUAGE DISORDER WITH OROFACIAL DYSPRAXIA", "Speech and language disorder with orofacial dyspraxia", "speech and language disorder with orofacial dyspraxia", "developmental disorder speech and language dyspraxias verbal developmental"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood apraxia of speech", "shortest_name_length": 3}
{"curie": "MONDO:0002249", "names": ["Elevated", "thrombocytoses", "Thrombocytosis", "Thrombocytoses", "THROMBOCYTOSIS", "thrombocytosis", "Thrombocythemia", "THROMBOCYTHEMIA", "thrombocythemia", "Thrombocythaemia", "thrombocythaemia", "Thrombocythemias", "THROMBOCYTHAEMIA", "Thrombocytosis NOS", "PLATELETS ELEVATED", "increased platelet", "high platelet count", "increased platelets", "High Platelet Count", "Increased platelets", "platelets increased", "Thrombocythemia NOS", "Platelet count high", "Platelets increased", "PLATELETS INCREASED", "Thrombocythemia, NOS", "Thrombocythaemia, NOS", "thrombocytosis disease", "elevated Platelet count", "Elevated Platelet Count", "Elevated platelet count", "elevated platelet count", "Increased platelet count", "increased platelet count", "INCREASED PLATELET COUNT", "Platelet Count Increased", "Platelet count increased", "Thrombocytosis (disorder)", "thrombocytosis (diagnosis)", "Thrombocyte count increased", "Increased number of platelets", "Platelet count above reference range", "Increased number of platelets in blood", "Platelet count above reference range (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombocytosis disease", "shortest_name_length": 8}
{"curie": "UMLS:C2987179", "names": ["Pancreatic Mucinous-Cystic Neoplasm, Low Grade", "Pancreatic Mucinous-Cystic Neoplasm, Low-Grade", "Pancreatic Mucinous-Cystic Neoplasm with Low Grade Dysplasia", "Pancreatic Mucinous Cystic Neoplasm with Low Grade Dysplasia", "Pancreatic Mucinous Cystic Neoplasm with Low-Grade Dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Mucinous-Cystic Neoplasm, Low Grade", "shortest_name_length": 46}
{"curie": "UMLS:C4087319", "names": ["Selective eating disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Selective eating disorder", "shortest_name_length": 25}
{"curie": "MONDO:0000393", "names": ["Partial Fetal Alcohol Syndrome", "partial fetal alcohol syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial fetal alcohol syndrome", "shortest_name_length": 30}
{"curie": "UMLS:C5420816", "names": ["Uveal Melanocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uveal Melanocytoma", "shortest_name_length": 18}
{"curie": "UMLS:C4289815", "names": ["Cervical Neuroendocrine Tumor G2", "Cervical Low Grade Neuroendocrine Tumor, Grade 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Neuroendocrine Tumor G2", "shortest_name_length": 32}
{"curie": "UMLS:C1707758", "names": ["Direct Contact Transmission Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Direct Contact Transmission Infection", "shortest_name_length": 37}
{"curie": "UMLS:C5239488", "names": ["Locally Advanced Oral Cavity Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Oral Cavity Squamous Cell Carcinoma", "shortest_name_length": 52}
{"curie": "MONDO:0005336", "names": ["Myopathy", "MYOPATHY", "myopathy", "MYOPATHIES", "myopathies", "Myopathies", "Myopathy, NOS", "MUSCLE DISEASE", "muscle disease", "DISORDER MUSCLE", "Muscle Disorder", "Disorder muscle", "muscle disorder", "Muscle disorder", "MUSCLE DISORDER", "Muscular Disease", "muscular disease", "muscle disorders", "Muscle disorders", "Muscle Disorders", "Myopathic changes", "Muscles--Diseases", "Myopathic disease", "muscular diseases", "Muscular Diseases", "muscular disorder", "Disorder of muscle", "Muscular Disorders", "disorder of muscle", "muscular disorders", "Muscle disorder NOS", "Myopathic Condition", "myopathy unspecified", "Disorders of muscles", "Myopathic Conditions", "Muscle tissue disease", "Myopathy, unspecified", "myopathies (diagnosis)", "Myopathic disease, NOS", "skeletal muscle disease", "Skeletal muscle disease", "Disorder of muscle, NOS", "Myopathic syndrome, NOS", "skeletal muscle disorder", "Muscle disease or syndrome", "disease (or disorder); muscle", "Myopathic disease or syndrome", "disorder of muscle (diagnosis)", "Disorders of muscles (M60-M63)", "Unspecified disorder of muscle", "Disorder of muscle, unspecified", "Myopathic Diseases and Syndromes", "Disorder of skeletal AND/OR smooth muscle", "Disorder of skeletal AND/OR smooth muscle (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy", "shortest_name_length": 8}
{"curie": "MONDO:0008692", "names": ["ABL", "MTP deficiency", "acanthocytosis", "Acanthocytosis", "ACANTHOCYTOSIS", "MTP DEFICIENCY", "Acanthocytoses", "Bassen-Kornzweig", "ABETALIPOPROTEINEMIA", "Abetalipoproteinemia", "abetalipoproteinemia", "Abetalipoproteinaemia", "Bassen Kornzweig Disease", "Bassen-Kornzweig disease", "Bassen-Kornzweig Disease", "bassen-kornzweig disease", "Bassen-Kornzweig Syndrome", "bassen kornzweig syndrome", "BASSEN-KORNZWEIG SYNDROME", "BASSEN KORNZWEIG SYNDROME", "Bassen Kornzweig Syndrome", "bassen-kornzweig syndrome", "Bassen-Kornzweig syndrome", "Bassen Kornzweig syndrome", "ABL - Abetalipoproteinemia", "Apolipoprotein B deficiency", "Apolipoprotein B Deficiency", "ABL - Abetalipoproteinaemia", "apolipoprotein B deficiency", "Apolipoprotein B Deficiencies", "Abetalipoproteinemia (disorder)", "abetalipoproteinemia neuropathy", "familial hypobetalipoproteinemia", "abetalipoproteinemia (diagnosis)", "betalipoprotein deficiency disease", "Betalipoprotein deficiency disease", "Betalipoprotein Deficiency Disease", "Disease, Betalipoprotein Deficiency", "Deficiency Disease, Betalipoprotein", "Apolipoprotein B Deficiency Disease", "Betalipoprotein Deficiency Diseases", "Deficiency Diseases, Betalipoprotein", "Diseases, Betalipoprotein Deficiency", "Hypobetalipoproteinemia, Familial, Apo B", "Homozygous familial hypobetalipoproteinemia", "homozygous familial hypobetalipoproteinemia", "Homozygous familial hypobetalipoproteinaemia", "congenital betalipoprotein deficiency syndrome", "Congenital betalipoprotein deficiency syndrome", "MICROSOMAL TRIGLYCERIDE TRANSFER PROTEIN DEFICIENCY", "Microsomal Triglyceride Transfer Protein Deficiency", "microsomal triglyceride transfer Protein deficiency", "Hypobetalipoproteinemia, Familial, Apolipoprotein B", "Abetalipoproteinemia, Normotriglyceridemic, Steinbert Type", "Microsomal Triglyceride Transfer Protein Deficiency Disease", "microsomal triglyceride transfer protein deficiency disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "abetalipoproteinemia", "shortest_name_length": 3}
{"curie": "MONDO:0015235", "names": ["De Die-Smulders-Vles-Fryns syndrome", "De Die, Smulders, Vles, Fryns syndrome", "arachnodactyly - intellectual disability - dysmorphism", "Arachnodactyly-intellectual disability-dysmorphism syndrome", "arachnodactyly-intellectual disability-dysmorphism syndrome", "Arachnodactyly and intellectual disability with facial dysmorphism syndrome", "arachnodactyly and intellectual disability with facial dysmorphism syndrome", "Arachnodactyly and intellectual disability with facial dysmorphism syndrome (disorder)", "arachnodactyly and intellectual disability with facial dysmorphism syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arachnodactyly-intellectual disability-dysmorphism syndrome", "shortest_name_length": 35}
{"curie": "MONDO:0019257", "names": ["JH", "JHH", "HFE2", "Hemochromatosis type 2", "hemochromatosis type 2", "Haemochromatosis type 2", "HEMOCHROMATOSIS, TYPE 2", "Hemochromatosis, type 2", "Juvenile hemochromatosis", "juvenile hemochromatosis", "hemochromatosis juvenile", "Juvenile haemochromatosis", "HEMOCHROMATOSIS, JUVENILE", "Hemochromatosis, juvenile", "iron overload disease juvenile", "Juvenile hemochromatosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemochromatosis type 2", "shortest_name_length": 2}
{"curie": "UMLS:C0269389", "names": ["Miscarriage in second trimester", "2nd Trimester Spontaneous Abortion", "ABORTION SPONTANEOUS SECOND TRIMESTER", "Second Trimester Spontaneous Abortion", "spontaneous abortion in second trimester", "Spontaneous abortion in second trimester", "Miscarriage in second trimester (disorder)", "spontaneous abortion in second trimester (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Miscarriage in second trimester", "shortest_name_length": 31}
{"curie": "MONDO:0008507", "names": ["SPA2", "Spa5", "Spa2", "SPA5", "surface polypeptides, anonymous", "SURFACE POLYPEPTIDES, ANONYMOUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "surface polypeptides, anonymous", "shortest_name_length": 4}
{"curie": "MONDO:0007228", "names": ["brachymesomelia renal syndrome", "brachymesomelia-renal syndrome", "BRACHYMESOMELIA-RENAL SYNDROME", "Brachymesomelia renal syndrome", "Brachymesomelia-renal syndrome", "Langer Nishino Yamaguchi syndrome", "severe upper limb brachymesomelia, glomerulocystic renal dysplasia, cranial and facial abnormalities, corneal opacities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachymesomelia-renal syndrome", "shortest_name_length": 30}
{"curie": "UMLS:C0752201", "names": ["Autosomal Recessive Familial Dystonia", "Familial Dystonia, Autosomal Recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Autosomal Recessive Familial Dystonia", "shortest_name_length": 37}
{"curie": "UMLS:C0751663", "names": ["Canavan Disease, Familial Form", "Familial Form of Canavan Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Canavan Disease, Familial Form", "shortest_name_length": 30}
{"curie": "UMLS:C1332180", "names": ["Adult Acute Lymphoid Leukemia in Partial Remission", "Adult Acute Lymphocytic Leukemia in Partial Remission", "Adult Acute Lymphogenous Leukemia in Partial Remission", "Acute Lymphoblastic Leukemia (ALL) in Partial Remission", "Adult Acute Lymphoblastic Leukemia in Partial Remission", "Adult Precursor Lymphoblastic Leukemia in Partial Remission"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Acute Lymphoblastic Leukemia in Partial Remission", "shortest_name_length": 50}
{"curie": "UMLS:C1335902", "names": ["Salivary Gland Inverted Ductal Papilloma", "inverted ductal papilloma of salivary gland", "inverted ductal papilloma of salivary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inverted ductal papilloma of salivary gland", "shortest_name_length": 40}
{"curie": "MONDO:0035400", "names": ["Seronegative AIH", "seronegative autoimmune hepatitis", "autoantibody-negative autoimmune hepatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "seronegative autoimmune hepatitis", "shortest_name_length": 16}
{"curie": "MONDO:0007577", "names": ["SCHATZKI SYNDROME", "Lower esophageal ring", "lower esophageal ring", "esophageal ring, lower", "ESOPHAGEAL RING, LOWER", "lower oesophageal ring", "Lower oesophageal ring", "Esophageal Ring, Lower", "ESOPHAGOGASTRIC RING SYNDROME", "LOWER ESOPHAGEAL RING SYNDROME", "Lower esophageal ring (disorder)", "lower esophageal ring (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophageal ring, lower", "shortest_name_length": 17}
{"curie": "MONDO:0021475", "names": ["benign nasal cavity tumor", "Benign Nasal Cavity Tumor", "benign nasal cavity neoplasm", "Benign Tumor of Nasal Cavity", "nasal cavity benign neoplasm", "Benign tumor of nasal cavity", "benign tumor of nasal cavity", "Benign Nasal Cavity Neoplasm", "Benign tumour of nasal cavity", "Benign Neoplasm of Nasal Cavity", "benign neoplasm of nasal cavity", "Benign neoplasm of nasal cavity", "Benign Tumor of the Nasal Cavity", "benign tumor of the nasal cavity", "benign neoplasm of the nasal cavity", "Benign Neoplasm of the Nasal Cavity", "Benign neoplasm of nasal cavity, NOS", "Benign neoplasm of nasal cavity (disorder)", "benign neoplasm of nasal cavity (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of nasal cavity", "shortest_name_length": 25}
{"curie": "MONDO:0018430", "names": ["partial corpus callosum agenesis-cerebellar vermis hypoplasia with posterior fossa cysts syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial corpus callosum agenesis-cerebellar vermis hypoplasia with posterior fossa cysts syndrome", "shortest_name_length": 97}
{"curie": "MONDO:0009574", "names": ["megalencephaly with dysmyelination", "Megalencephaly with Dysmyelination", "MEGALENCEPHALY WITH DYSMYELINATION", "Megalencephaly with Diffuse White Matter Hypodensity", "megalencephaly with diffuse white matter hypodensity", "MEGALENCEPHALY WITH DIFFUSE WHITE MATTER HYPODENSITY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "megalencephaly with dysmyelination", "shortest_name_length": 34}
{"curie": "UMLS:C1511282", "names": ["Breast Adenohibernoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Adenohibernoma", "shortest_name_length": 21}
{"curie": "MONDO:0002372", "names": ["ovarian monodermal and highly specialized teratoma", "Ovarian Monodermal and Highly Specialized teratoma", "Ovarian Monodermal and Highly Specialized Teratoma", "monodermal and highly specialized teratoma, ovarian", "teratoma, monodermal and highly specialized, ovarian", "Ovarian Germ Cell Monodermal and Highly Specialized Teratoma", "ovarian germ cell monodermal and highly specialized teratoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian monodermal and highly specialized teratoma", "shortest_name_length": 50}
{"curie": "MONDO:0004081", "names": ["bile duct clear cell carcinoma", "Clear Cell Bile Duct Adenocarcinoma", "Bile duct clear cell adenocarcinoma", "bile duct clear cell adenocarcinoma", "clear cell bile duct adenocarcinoma", "Bile Duct Clear Cell Adenocarcinoma", "Clear Cell Adenocarcinoma of Bile Duct", "clear cell adenocarcinoma of bile duct", "clear cell adenocarcinoma of the bile duct", "Clear Cell Adenocarcinoma of the Bile Duct", "Extrahepatic Bile Duct Clear Cell Adenocarcinoma", "extrahepatic bile duct clear cell adenocarcinoma", "clear cell adenocarcinoma of extrahepatic bile duct", "clear cell adenocarcinoma of extrahepatic bile duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extrahepatic bile duct clear cell adenocarcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0020838", "names": ["anterior nasal diphtheria", "Anterior Nasal Diphtheria", "Anterior nasal diphtheria", "Diphtheria, anterior nasal", "diphtheria; nasal, anterior", "nasal, anterior; diphtheritic", "Anterior nasal diphtheria (disorder)", "anterior nasal diphtheria (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anterior nasal diphtheria", "shortest_name_length": 25}
{"curie": "UMLS:C4763549", "names": ["Metastatic Extracranial Malignant Solid Tumor", "Metastatic Extracranial Malignant Solid Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Extracranial Malignant Solid Neoplasm", "shortest_name_length": 45}
{"curie": "UMLS:C1562503", "names": ["Galen Malformations Veins", "Malformations Vein, Galen", "Vein of Galen Malformation", "Malformations Veins, Galen", "Vein of Galen malformation", "Vein Of Galen Malformation", "Vein of Galen Malformations", "Vein of Galen malformation (disorder)", "Vein of Galen malformation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vein of Galen Malformations", "shortest_name_length": 25}
{"curie": "UMLS:C1853723", "names": ["Mpd2", "VCPDM", "Distal myopathy 2", "MYOPATHY, DISTAL 2", "Myopathy, Distal 2", "Matrin 3 distal myopathy", "Matrin 3 Distal Myopathy", "Myopathia Distalis Type 2", "Myopathia distalis type 2", "Distal myopathy 2 (disorder)", "MATR3-related distal myopathy", "Distal myopathy with vocal cord weakness", "Distal Myopathy with Vocal Cord Weakness", "Vocal cord and pharyngeal distal myopathy", "VCPDM - vocal cord and pharyngeal distal myopathy", "Distal Myopathy with Vocal Cord and Pharyngeal Signs", "Vocal Cord and Pharyngeal Weakness with Distal Myopathy", "Vocal Cord and Pharyngeal Dysfunction with Distal Myopathy", "Vocal cord and pharyngeal dysfunction with distal myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MYOPATHY, DISTAL 2", "shortest_name_length": 4}
{"curie": "MONDO:0004076", "names": ["tendon sheath lipoma", "Tendon Sheath Lipoma", "Lipoma of Tendon Sheath", "lipoma of tendon sheath", "Lipoma of the Tendon Sheath", "lipoma of the tendon sheath"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tendon sheath lipoma", "shortest_name_length": 20}
{"curie": "UMLS:C0343652", "names": ["Anogenital papillomaviral intraepithelial neoplasia", "Anogenital Papillomaviral Intraepithelial Neoplasia", "Anogenital papillomaviral intraepithelial neoplasia (disorder)", "Anogenital papillomaviral intraepithelial neoplasia (diagnosis)", "human papilloma virus infection anogenital intraepithelial neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anogenital papillomaviral intraepithelial neoplasia", "shortest_name_length": 51}
{"curie": "MONDO:0008633", "names": ["MWS", "CAPS2", "UDA Syndrome", "Uda syndrome", "UDA SYNDROME", "UDA Syndromes", "Syndrome, UDA", "muckle well syndrome", "Muckle-Wells Syndrome", "Muckle-Wells syndrome", "MUCKLE-Wells syndrome", "Muckle Wells Syndrome", "muckle-wells syndrome", "MUCKLE-WELLS SYNDROME", "Muckle Wells syndrome", "Neutrophilic urticaria", "Syndrome, Muckle-Wells", "neutrophilic urticaria", "Muckle-Wells syndrome (MWS)", "Muckle-Wells type amyloidosis", "Neutrophilic urticaria (disorder)", "Urticaria, Deafness and Amyloidosis", "urticaria, deafness and amyloidosis", "urticaria-deafness-amyloidosis syndrome", "Muckle-Wells syndrome (MWS) (diagnosis)", "Urticaria Deafness Amyloidosis Syndrome", "URTICARIA-DEAFNESS-AMYLOIDOSIS SYNDROME", "Urticaria-Deafness-Amyloidosis Syndrome", "Urticaria-Deafness-Amyloidosis Syndromes", "CRYOPYRIN-ASSOCIATED PERIODIC SYNDROME 2", "Syndrome, Urticaria-Deafness-Amyloidosis", "Cryopyrin-associated periodic syndrome 2", "Amyloid nephropathy with deafness and urticaria", "Familial amyloid nephropathy with urticaria AND deafness", "Familial amyloid nephropathy with urticaria and deafness", "Urticaria, deafness and amyloidosis syndrome (Muckle and Wells)", "Familial amyloid nephropathy with urticaria AND deafness (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Muckle-Wells syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0004170", "names": ["nodular episcleritis", "Nodular episcleritis", "episcleritis nodular", "Nodular episcleritis (disorder)", "Nodular episcleritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nodular episcleritis", "shortest_name_length": 20}
{"curie": "MONDO:0003860", "names": ["C-P Angle Meningioma", "C-P angle meningioma", "Meningioma of C-P Angle", "meningioma of C-P angle", "Meningioma of the C-P Angle", "meningioma of the C-P angle", "cerebellopontine angle meningioma", "Cerebellopontine angle meningioma", "Cerebellopontine Angle Meningioma", "Cerebellar Pontine Angle Meningioma", "cerebellar Pontine angle meningioma", "meningioma of cerebellopontine angle", "Meningioma of Cerebellopontine Angle", "meningioma of cerebellar Pontine angle", "Meningioma of Cerebellar Pontine Angle", "Meningioma of the Cerebellopontine Angle", "meningioma of the cerebellopontine angle", "meningioma of the Cerebellar Pontine Angle", "meningioma of the cerebellar Pontine angle", "Meningioma of the Cerebellar Pontine Angle", "cerebellopontine angle meningioma (disease)", "Cerebellopontine angle meningioma (disorder)", "meningioma (disease) of cerebellopontine angle", "meningioma of cerebellopontine angle (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellopontine angle meningioma", "shortest_name_length": 20}
{"curie": "UMLS:C1531582", "names": ["Anterior Segment Ischemia", "anterior segment ischemia", "Anterior segment ischemia", "Anterior segment ischaemia", "Anterior segment ischemia (disorder)", "anterior segment ischemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anterior segment ischemia", "shortest_name_length": 25}
{"curie": "MONDO:0001730", "names": ["urethra syndrome", "URETHRA SYNDROME", "Urethral syndrome", "urethral syndrome", "syndrome urethral", "urethral; syndrome", "syndrome; urethral", "Urethral syndrome NOS", "Urethral syndrome, NOS", "Urethral syndrome (disorder)", "urethral syndrome (diagnosis)", "Urethral syndrome, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urethral syndrome", "shortest_name_length": 16}
{"curie": "UMLS:C4722085", "names": ["Colorectal cancer", "Malignant neoplasm of colon and/or rectum", "Malignant neoplasm of colon and/or rectum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant neoplasm of colon and/or rectum", "shortest_name_length": 17}
{"curie": "MONDO:0011489", "names": ["SPG12", "spastic paraplegia 12", "hereditary spastic paraplegia 12", "RTN2 hereditary spastic paraplegia", "hereditary spastic paraplegia type 12", "autosomal dominant spastic paraplegia 12", "Spastic paraplegia 12, autosomal dominant", "SPASTIC PARAPLEGIA 12, AUTOSOMAL DOMINANT", "spastic paraplegia 12, autosomal dominant", "autosomal dominant spastic paraplegia type 12", "Autosomal dominant spastic paraplegia type 12", "familial spastic paraplegia autosomal dominant type 12", "Autosomal dominant spastic paraplegia type 12 (disorder)", "hereditary spastic paraplegia caused by mutation in RTN2", "Autosomal dominant spastic paraplegia type 12 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 12", "shortest_name_length": 5}
{"curie": "MONDO:0004872", "names": ["pile", "Piles", "piles", "Piles, NOS", "HEMORRHOID", "hemorrhoid", "Hemorrhoid", "HEMORRHOIDS", "hemorrhoids", "Haemorrhoid", "haemorrhoid", "Hemorrhoids", "haemorrhoids", "Haemorrhoids", "HAEMORRHOIDS", "Hemorrhoids NOS", "Hemorrhoids, NOS", "hemorrhoid (pile)", "Haemorrhoids, NOS", "Piles - hemorrhoids", "Piles - haemorrhoids", "hemorrhoidal disease", "Hemorrhoids (disorder)", "Hemorrhoids (diagnosis)", "hemorrhoids (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemorrhoid", "shortest_name_length": 4}
{"curie": "MONDO:0002847", "names": ["skeletal muscle cancer", "skeletal muscle tissue cancer", "malignant skeletal muscle tumor", "Malignant Skeletal Muscle Tumor", "cancer of skeletal muscle tissue", "malignant tumor of skeletal muscle", "malignant tumor of Skeletal Muscle", "Malignant Tumor of Skeletal Muscle", "Malignant Skeletal Muscle Neoplasm", "malignant skeletal muscle neoplasm", "malignant neoplasm of skeletal muscle", "Malignant Neoplasm of Skeletal Muscle", "Malignant Tumor of the Skeletal Muscle", "malignant tumor of the skeletal muscle", "malignant skeletal muscle tissue neoplasm", "Malignant Neoplasm of the Skeletal Muscle", "malignant neoplasm of the skeletal muscle", "malignant neoplasm of skeletal muscle tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skeletal muscle cancer", "shortest_name_length": 22}
{"curie": "MONDO:0012176", "names": ["Emanuel syndrome", "EMANUEL SYNDROME", "Der(22)t(11;22) syndrome", "supernumerary Der(22)T(11", "Supernumary Der(22) Syndrome", "supernumerary der(22) syndrome", "Supernumerary der(22) syndrome", "Supernumary Der(22)T(11;22) Syndrome", "Supernumerary der(22)t(11;22) syndrome", "SUPERNUMERARY DER(22)t(11;22) SYNDROME", "Ehlers-Danlos syndrome, classic-like, 1", "supernumerary der(22),t(11;22) syndrome", "Supernumary Derivative 22 Chromosome Syndrome", "Supernumerary derivative 22 chromosome syndrome", "Supernumerary der(22)t(11;22) syndrome (disorder)", "Der(22) syndrome due to 3:1 meiotic disjunction events", "Der(22) Syndrome Due To 3:1 Meiotic Disjunction Events"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Emanuel syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0007522", "names": ["cEDS", "EDS I", "EDS II", "Classical EDS", "EDS I, formerly", "EDS II, formerly", "EDS, classic type", "Classical EDS (cEDS)", "Ehlers-Danlos syndrome type 2", "classic Ehlers-Danlos syndrome", "Ehlers-Danlos syndrome, type I", "Ehlers-Danlos syndrome, type II", "classical Ehlers-Danlos syndrome", "Classical Ehlers-Danlos syndrome", "Ehlers Danlos syndrome, mitis type", "Ehlers-Danlos syndrome classic type", "Ehlers-Danlos syndrome, gravis type", "Ehlers-Danlos syndrome, classic type", "EHLERS-DANLOS SYNDROME, CLASSIC TYPE", "Ehlers-Danlos syndrome classical type", "Ehlers-Danlos syndrome type 2 (formerly)", "Ehlers-Danlos syndrome, type I, formerly", "Ehlers-Danlos syndrome type 1 (formerly)", "Ehlers-Danlos syndrome, type II, formerly", "Ehlers Danlos syndrome, mild classic type", "Ehlers-Danlos syndrome, severe classic type", "Classical Ehlers-Danlos syndrome (diagnosis)", "Ehlers Danlos syndrome, mitis type, formerly", "Ehlers-Danlos syndrome, gravis type, formerly", "Ehlers-Danlos syndrome classic type (disorder)", "Ehlers Danlos syndrome, mild classic type, formerly", "Ehlers-Danlos syndrome, severe classic type, formerly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ehlers-Danlos syndrome, classic type", "shortest_name_length": 4}
{"curie": "UMLS:C0334102", "names": ["Lymphangiomatosis", "lymphangiomatosis", "Lymphangiomatosis (disorder)", "Lymphangiomatosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphangiomatosis", "shortest_name_length": 17}
{"curie": "MONDO:0002224", "names": ["OVARIAN CYST MALIGNANT", "Malignant Ovarian Cyst", "Malignant ovarian cyst", "malignant ovarian cyst", "Ovarian cyst malignant", "malignant ovarian cyst (disease)", "ovarian cyst (disease), malignant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant ovarian cyst", "shortest_name_length": 22}
{"curie": "UMLS:C0856010", "names": ["Relapsed MALT Type Extranodal Marginal Zone B-Cell Lymphoma", "Recurrent Extranodal Marginal Zone B-Cell Lymphoma (MALT Type)", "Extranodal marginal zone B-cell lymphoma (MALT type) recurrent", "Relapsed Extranodal Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue", "Recurrent Extranodal Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue", "Recurrent Extranodal Marginal Zone B-Cell Lymphoma of Mucosa-Associated Lymphoid Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extranodal marginal zone B-cell lymphoma (MALT type) recurrent", "shortest_name_length": 59}
{"curie": "UMLS:C0855263", "names": ["Somatic Type Delusional Disorder", "Delusional disorder, somatic type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Delusional disorder, somatic type", "shortest_name_length": 32}
{"curie": "MONDO:0002201", "names": ["Vulvar Trichoblastoma", "vulvar trichoblastoma", "Vulvar Trichoepithelioma", "vulvar trichoepithelioma", "mammalian vulva trichoblastoma", "trichoblastoma of mammalian vulva"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar trichoepithelioma", "shortest_name_length": 21}
{"curie": "UMLS:C4049883", "names": ["Stenotic", "Obstructive Ureterocele"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Obstructive Ureterocele", "shortest_name_length": 8}
{"curie": "MONDO:0020178", "names": ["palpebral lentiginosis", "skin of eyelid lentigo"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "palpebral lentiginosis", "shortest_name_length": 22}
{"curie": "UMLS:C5419794", "names": ["Colorectal Poorly Cohesive Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Poorly Cohesive Adenocarcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0021299", "names": ["Extrahepatic bile duct cancer stage 0", "stage 0 extrahepatic bile duct cancer", "Extrahepatic Bile Duct Cancer Stage 0", "Stage 0 Extrahepatic Bile Duct Cancer", "extrahepatic bile duct cancer stage 0", "stage 0 extrahepatic bile duct carcinoma", "extrahepatic bile duct carcinoma in situ", "Extrahepatic bile duct carcinoma in situ", "Extrahepatic Bile Duct Carcinoma in situ", "Stage 0 Extrahepatic Bile Duct Carcinoma", "extrahepatic bile duct in situ carcinoma", "Carcinoma in situ of Extrahepatic Bile Duct", "carcinoma in situ of extrahepatic bile duct", "stage 0 carcinoma of extrahepatic bile duct", "Extrahepatic Biliary Duct Carcinoma in situ", "Stage 0 Carcinoma of Extrahepatic Bile Duct", "extrahepatic biliary duct carcinoma in situ", "Carcinoma in situ of extrahepatic bile duct", "Carcinoma in situ of Extrahepatic Bile Ducts", "Carcinoma in situ of extrahepatic bile ducts", "carcinoma in situ of extrahepatic bile ducts", "Carcinoma in situ of Extrahepatic Biliary Ducts", "stage 0 carcinoma of the extrahepatic bile duct", "carcinoma in situ of the extrahepatic bile duct", "carcinoma in situ of extrahepatic biliary ducts", "Stage 0 Carcinoma of the Extrahepatic Bile Duct", "Carcinoma in situ of the Extrahepatic Bile Duct", "stage 0 extrahepatic bile duct carcinoma in situ", "Carcinoma in situ of extrahepatic bile ducts, NOS", "Carcinoma in situ of extrahepatic bile ducts (disorder)", "carcinoma in situ of extrahepatic bile duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma in situ of extrahepatic bile duct", "shortest_name_length": 37}
{"curie": "MONDO:0018751", "names": ["genetic otorhinolaryngologic disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genetic otorhinolaryngologic disease", "shortest_name_length": 36}
{"curie": "MONDO:0005473", "names": ["TMD", "disease tmj", "TMJ Disease", "tmj disease", "TMJ Diseases", "tmj disorder", "Disease, TMJ", "TMJ Disorder", "TMJ Disorders", "Disorder, TMJ", "Diseases, TMJ", "disorders tmj", "tmj disorders", "Disorders, TMJ", "temporomandibular disorder", "disorder temporomandibular", "Temporomandibular Disorder", "disorders temporomandibular", "Temporomandibular disorders", "temporomandibular disorders", "Disorder, Temporomandibular", "Temporomandibular Disorders", "Disorders, Temporomandibular", "temporomandibular joint disease", "TEMPOROMANDIBULAR JOINT DISEASE", "Temporomandibular Joint Disease", "Temporomandibular joint disorder", "Disease, Temporomandibular Joint", "TEMPOROMANDIBULAR JOINT DISORDER", "Joint Disease, Temporomandibular", "temporomandibular joint diseases", "jaw; disorder, temporomandibular", "Temporomandibular Joint Diseases", "temporomandibular joint disorder", "Temporomandibular Joint Disorder", "disorder joint temporomandibular", "Temporomandibular joint--Diseases", "Disorder, Temporomandibular Joint", "Joint Diseases, Temporomandibular", "Temporomandibular Joint Disorders", "Diseases, Temporomandibular Joint", "Joint Disorder, Temporomandibular", "Temporomandibular joint disorders", "disorders joint temporomandibular", "temporomandibular; disorder, joint", "TEMPORAL MANDIBULAR JOINT DISORDER", "Disorders, Temporomandibular Joint", "Joint Disorders, Temporomandibular", "Temporomandibular joint disorder NOS", "Temporomandibular joint disorder, NOS", "TMJ - Temporomandibular joint disorder", "Temporomandibular joint disorder (disorder)", "temporomandibular joint disorder (diagnosis)", "Temporomandibular joint disorder, unspecified", "disease (or disorder); temporomandibular joint", "Temporomandibular joint disorders, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "temporomandibular joint disorder", "shortest_name_length": 3}
{"curie": "UMLS:C5419011", "names": ["Non-Neoplastic Endocrine Pancreas Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Endocrine Pancreas Disorder", "shortest_name_length": 42}
{"curie": "UMLS:C1336415", "names": ["stage IV extragonadal non-seminomatous germ cell tumor", "Stage IV Extragonadal Non-Seminomatous Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Extragonadal Non-Seminomatous Germ Cell Tumor", "shortest_name_length": 54}
{"curie": "UMLS:C4054408", "names": ["Nephropathy Associated with Rhabdomyolysis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephropathy Associated with Rhabdomyolysis", "shortest_name_length": 42}
{"curie": "MONDO:0012523", "names": ["RP36", "RP 36", "Retinitis Pigmentosa 36", "retinitis pigmentosa 36", "RETINITIS PIGMENTOSA 36", "PRCD retinitis pigmentosa", "retinitis pigmentosa type 36", "retinitis pigmentosa caused by mutation in PRCD"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 36", "shortest_name_length": 4}
{"curie": "MONDO:0020361", "names": ["partial cryptophthalmia", "incomplete cryptophthalmos"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial cryptophthalmia", "shortest_name_length": 23}
{"curie": "UMLS:C0563312", "names": ["IgM MGUS", "IgM monoclonal gammopathy of uncertain significance", "IgM monoclonal gammopathy of undetermined significance", "IgM Monoclonal Gammopathy of Undetermined Significance", "monoclonal gammopathy of undetermined significance IgM", "Immunoglobulin M monoclonal gammopathy of uncertain significance", "IgM monoclonal gammopathy of undetermined significance (diagnosis)", "Immunoglobulin M monoclonal gammopathy of undetermined significance", "Immunoglobulin M monoclonal gammopathy of uncertain significance (disorder)", "Immunoglobulin M monoclonal gammopathy of undetermined significance (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IgM monoclonal gammopathy of uncertain significance", "shortest_name_length": 8}
{"curie": "MONDO:0017701", "names": ["GSDIV, adult neuromuscular form", "GSD type 4, adult neuromuscular form", "GBE deficiency, adult neuromuscular form", "glycogenosis type 4, adult neuromuscular form", "glycogenosis type IV, adult neuromuscular form", "glycogen storage disease type 4, adult neuromuscular form", "glycogen storage disease type IV, adult neuromuscular form", "GSD due to glycogen branching enzyme deficiency, adult neuromuscular form", "glycogenosis due to glycogen branching enzyme deficiency, adult neuromuscular form", "glycogen storage disease due to glycogen branching enzyme deficiency, adult neuromuscular form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease due to glycogen branching enzyme deficiency, adult neuromuscular form", "shortest_name_length": 31}
{"curie": "UMLS:C0749095", "names": ["SUBDURAL HEMATOMA CHRONIC", "Chronic subdural hematoma", "Chronic Subdural Hematoma", "chronic subdural hemotoma", "chronic subdural hematoma", "Chronic Subdural Hematomas", "chronic subdural haematoma", "Chronic subdural haematoma", "Subdural Hematoma, Chronic", "chronic subdural hematomas", "Hematoma, Chronic Subdural", "Hematoma, Subdural, Chronic", "Subdural Hematomas, Chronic", "subdural hemorrhage chronic", "Hematomas, Chronic Subdural", "chronic subdural hemorrhage", "Hemorrhage, Subdural, Chronic", "chronic subdural hematoma (diagnosis)", "subdural hemorrhage chronic (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hematoma, Subdural, Chronic", "shortest_name_length": 25}
{"curie": "UMLS:C4330971", "names": ["Stage III HPV-Mediated (p16-Positive) Oropharyngeal Throat Cancer", "Pathologic Stage III HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage III HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8", "shortest_name_length": 65}
{"curie": "MONDO:0013190", "names": ["factor XIIIB deficiency", "Reduced factor XIII, subunit B", "Factor XIII subunit B deficiency", "factor XIII, b subunit, deficiency of", "FACTOR XIII, B SUBUNIT, DEFICIENCY OF", "Factor XIII, B Subunit, Deficiency Of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "factor XIII, b subunit, deficiency of", "shortest_name_length": 23}
{"curie": "MONDO:0014416", "names": ["AIMAH2", "primary macronodular adrenal hyperplasia", "PRIMARY MACRONODULAR ADRENAL HYPERPLASIA", "ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA 2", "ACTH-independent macronodular adrenal hyperplasia 2", "ACTH-independent macronodular adrenal hyperplasia type 2", "ARMC5 Cushing syndrome due to macronodular adrenal hyperplasia", "Cushing syndrome due to macronodular adrenal hyperplasia caused by mutation in ARMC5", "ACTH-independent macronodular adrenal hyperplasia 2, autosomal dominant, somatic mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ACTH-independent macronodular adrenal hyperplasia 2", "shortest_name_length": 6}
{"curie": "MONDO:0056820", "names": ["Sinonasal Neoplasm", "nasal cavity and paranasal sinus neoplasm", "Nasal Cavity and Paranasal Sinus Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasal cavity and paranasal sinus neoplasm", "shortest_name_length": 18}
{"curie": "MONDO:0015398", "names": ["hemifacial microsomia", "otomandibular syndrome", "Laterofacial microsomia", "otomandibular dysostosis", "first branchial arch syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemifacial microsomia", "shortest_name_length": 21}
{"curie": "MONDO:0010235", "names": ["PPMX", "PPM-X", "MRX16", "MRX79", "MRXS13", "PPM-X syndrome", "Ppm-X Syndrome", "Lindsay-Burn syndrome", "Lindsay Burn syndrome", "X-linked mental retardation 16", "X-linked mental retardation 79", "Mental Retardation, X-Linked 16", "mental retardation, X-linked 79", "mental retardation, X-linked 16", "MENTAL RETARDATION, X-LINKED 79", "Mental Retardation, X-Linked 79", "MENTAL RETARDATION, X-LINKED 16", "X-linked intellectual disability 79", "intellectual disability, X-linked 16", "intellectual disability, X-linked 79", "X-linked mental retardation, syndromic 13", "MENTAL RETARDATION, X-LINKED, SYNDROMIC 13", "mental retardation, X-linked, syndromic 13", "Mental Retardation, X-Linked, Syndromic 13", "X-linked mental retardation with spasticity", "mental retardation psychosis macroorchidism", "MENTAL RETARDATION, X-LINKED, WITH SPASTICITY", "Mental Retardation, X-Linked, With Spasticity", "mental retardation, X-linked, with spasticity", "X-linked mental retardation 16 (MRX16, XLMR16)", "mental retardation, X-linked, syndromic type 13", "intellectual disability, X-linked, syndromic 13", "intellectual disability psychosis macroorchidism", "X-linked intellectual disability with spasticity", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, 79", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, 16", "intellectual disability, X-linked, with spasticity", "intellectual disability, X-linked, syndromic type 13", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 13", "intellectual deficit, X-linked - psychosis - macroorchidism", "X-linked intellectual disability-psychosis-macroorchidism syndrome", "x-linked intellectual disability psychosis-macroorchidism syndrome", "mental retardation with psychosis, pyramidal signs, and macroorchidism", "MENTAL RETARDATION WITH PSYCHOSIS, PYRAMIDAL SIGNS, AND MACROORCHIDISM", "Mental Retardation with Psychosis, Pyramidal Signs, and Macroorchidism", "intellectual disability with psychosis, pyramidal signs, and macroorchidism", "PPMX - Mental retardation with psychosis, pyramidal signs, and macroorchidism", "X-linked intellectual disability-psychosis-macroorchidism syndrome (disorder)", "x-linked intellectual disability psychosis-macroorchidism syndrome (diagnosis)", "intellectual developmental disorder, X-linked, syndromic 13, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability-psychosis-macroorchidism syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C1519920", "names": ["Vaginal Endometrioid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Endometrioid Adenocarcinoma", "shortest_name_length": 35}
{"curie": "MONDO:0000715", "names": ["lymph node adenoid cystic cancer", "lymph node adenoid cystic carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymph node adenoid cystic carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0007020", "names": ["wernicke", "WERNICKE", "wernickes", "Wernicke disease", "Wernicke Disease", "wernicke syndrome", "disease wernickes", "Cerebral Beriberi", "Wernicke Syndrome", "Wernickes Syndrome", "Wernicke's Disease", "Beriberi, Cerebral", "wernicke's disease", "Wernicke's disease", "wernickes syndrome", "Wernicke's syndrome", "wernicke's syndrome", "Wernicke's Syndrome", "Wernicke Encephalopathy", "Wernicke encephalopathy", "GAYET-WERNICKE SYNDROME", "WERNICKE ENCEPHALOPATHY", "wernicke encephalopathy", "ENCEPHALOPATHY WERNICKE", "wernickes encephalopathy", "ENCEPHALOPATHY, WERNICKE", "Encephalopathy;wernickes", "encephalopathy wernickes", "Encephalopathy, Wernicke", "Wernicke Encephalopathies", "Encephalopathy, Wernickes", "Wernicke's Encephalopathy", "wernicke's encephalopathy", "Wernicke's encephalopathy", "encephalopathy wernicke's", "Encephalopathy, Wernicke's", "Encephalopathies, Wernicke", "Gayet-Wernicke Encephalopathy", "Gayet Wernicke Encephalopathy", "Wernicke's disease (disorder)", "Encephalopathy, Gayet Wernicke", "Encephalopathy, Gayet-Wernicke", "Wernicke's disease (diagnosis)", "WERNICKE ENCEPHALOPATHY SYNDROME", "dementia due to thiamine deficiency", "Korsakoff's psychosis, alcohol related", "Wernicke; disease or syndrome (manifestation)", "Wernicke Superior Hemorrhagic Polioencephalitis", "Wernicke Polioencephalitis, Superior Hemorrhagic", "Wernicke's Superior Hemorrhagic Polioencephalitis", "Wernicke's Polioencephalitis, Superior Hemorrhagic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wernicke encephalopathy", "shortest_name_length": 8}
{"curie": "MONDO:0013354", "names": ["SPAX4", "spastic ataxia 4", "spastic ataxia type 4", "autosomal recessive spastic ataxia 4", "SPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE", "spastic ataxia 4, autosomal recessive", "MTPAP autosomal recessive spastic ataxia", "Autosomal recessive spastic ataxia type 4", "autosomal recessive spastic ataxia type 4", "SPAX 4 - autosomal recessive spastic ataxia type 4", "autosomal recessive spastic ataxia caused by mutation in MTPAP", "autosomal recessive spastic ataxia - optic atrophy - dysarthria", "autosomal recessive spastic ataxia-optic atrophy-dysarthria syndrome", "Autosomal recessive spastic ataxia-optic atrophy-dysarthria syndrome", "Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome", "Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic ataxia 4", "shortest_name_length": 5}
{"curie": "UMLS:C1709035", "names": ["Minimally Invasive Thymoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Minimally Invasive Thymoma", "shortest_name_length": 26}
{"curie": "MONDO:0003370", "names": ["retroperitoneal leiomyosarcoma", "Retroperitoneal Leiomyosarcoma", "leiomyosarcoma of retroperitoneum", "retroperitoneal space leiomyosarcoma", "leiomyosarcoma of retroperitoneal space", "leiomyosarcoma of retroperitoneum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retroperitoneal leiomyosarcoma", "shortest_name_length": 30}
{"curie": "MONDO:0014458", "names": ["FRTS4", "FRTS4 with MODY", "FRTS4 WITH MODY", "HNF4A Fanconi syndrome", "Fanconi renotubular syndrome 4", "Fanconi syndrome caused by mutation in HNF4A", "FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THE YOUNG", "Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young", "FANCONI RENOTUBULAR SYNDROME 4, WITH MATURITY-ONSET DIABETES OF THE YOUNG", "fanconi renotubular syndrome 4, with maturity-onset diabetes of the young"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young", "shortest_name_length": 5}
{"curie": "MONDO:0010919", "names": ["Severe recurrent varicella", "varicella, severe recurrent", "Varicella, Severe Recurrent", "VARICELLA, SEVERE RECURRENT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "varicella, severe recurrent", "shortest_name_length": 26}
{"curie": "UMLS:C5669731", "names": ["Oligometastatic Colorectal Cancer", "Oligometastatic Colorectal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oligometastatic Colorectal Carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0013506", "names": ["SCZD16", "SCHIZOPHRENIA 16", "schizophrenia 16", "schizophrenia type 16", "CHROMOSOME 7q36.3 DUPLICATION SYNDROME, 362-KB", "chromosome 7Q36.3 Duplication syndrome, 362-Kb", "schizophrenia susceptibility locus, chromosome 7Q36.3-related", "SCHIZOPHRENIA SUSCEPTIBILITY LOCUS, CHROMOSOME 7q36.3-RELATED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schizophrenia 16", "shortest_name_length": 6}
{"curie": "MONDO:0020548", "names": ["scar; pemphigoid", "ocular pemphigoid", "Mucosal pemphigoid", "Scarring pemphigoid", "cicatricial pemphigoid", "Cicatricial Pemphigoid", "Cicatricial pemphigoid", "cicatricial; pemphigoid", "PEMPHIGOID, CICATRIZING", "pemphigoid; cicatricial", "Pemphigoid, Cicatricial", "Benign mucosal pemphigus", "Mucosynechial pemphigoid", "Benign mucosal pemphigoid", "mucosal pemphigoid benign", "Benign Mucosal Pemphigoid", "Mucosal Pemphigoid, Benign", "Mucous membrane pemphigoid", "Pemphigoid, Benign Mucosal", "PEMPHIGOID, BENIGN MUCOSAL", "mucous membrane pemphigoid", "Benign Mucosal Pemphigoids", "Pemphigoids, Benign Mucosal", "Mucosal Pemphigoids, Benign", "Benign mucous membrane pemphigoid", "benign membrane mucous pemphigoid", "Benign Mucous Membrane Pemphigoid", "Pemphigoid, Benign Mucous Membrane", "cicatricial pemphigoid (diagnosis)", "Mucous Membrane Pemphigoid, Benign", "eczema; bullous, mucosynechial, atrophic", "bullous; eczema, mucosynechial, atrophic", "Mucosynechia atrophic bullous dermatitis", "mucosynechial atrophic bullous dermatitis", "Mucosynechial atrophic bullous dermatitis", "Benign mucous membrane pemphigoid (disorder)", "mucosynechial atrophic bullous dermatitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ocular pemphigoid", "shortest_name_length": 16}
{"curie": "UMLS:C4289987", "names": ["CMO Type 2", "Aldosterone Synthase Deficiency Type 2", "Corticosterone Methyl Oxidase Deficiency Type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aldosterone Synthase Deficiency Type 2", "shortest_name_length": 10}
{"curie": "MONDO:0010493", "names": ["DBA14", "TSR2 Diamond-Blackfan anemia", "Diamond-Blackfan anemia caused by mutation in TSR2", "Diamond-Blackfan anemia 14 with mandibulofacial dysostosis", "DIAMOND-BLACKFAN ANEMIA 14 WITH MANDIBULOFACIAL DYSOSTOSIS", "DIAMOND-BLACKFAN ANEMIA, 14, WITH MANDIBULOFACIAL DYSOSTOSIS", "Diamond-Blackfan anemia 14 with mandibulofacial dysostosis, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diamond-Blackfan anemia 14 with mandibulofacial dysostosis", "shortest_name_length": 5}
{"curie": "UMLS:C1516075", "names": ["Astler-Coller C3 Rectal Carcinoma", "Astler-Coller C3 Carcinoma of Rectum", "Astler-Coller C3 Carcinoma of the Rectum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Astler-Coller C3 Rectal Carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0007103", "names": ["FALS", "ALS1", "ALS1 (diagnosis)", "AMYOTROPHIC LATERAL SCLEROSIS 1", "amyotrophic lateral sclerosis 1", "Amyotrophic lateral sclerosis 1", "Amyotrophic Lateral Sclerosis 1", "amyotrophic lateral sclerosis ALS1", "amyotrophic lateral sclerosis type 1", "amyotrophic lateral sclerosis, sporadic", "AMYOTROPHIC LATERAL SCLEROSIS, SPORADIC", "Amyotrophic Lateral Sclerosis, Sporadic", "amyotrophic lateral sclerosis, familial", "AMYOTROPHIC LATERAL SCLEROSIS 1, FAMILIAL", "amyotrophic lateral sclerosis 1, familial", "amyotrophic lateral sclerosis, susceptibility to", "Amyotrophic Lateral Sclerosis, Autosomal Dominant", "amyotrophic lateral sclerosis, autosomal dominant", "amyotrophic lateral sclerosis, sporadic, included", "amyotrophic lateral sclerosis 1, autosomal dominant", "AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL DOMINANT", "amyotrophic lateral sclerosis 1, autosomal recessive", "AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE", "amyotrophic lateral sclerosis 1, autosomal dominant amyotrophic lateral sclerosis 1, autosomal recessive, included"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyotrophic lateral sclerosis type 1", "shortest_name_length": 4}
{"curie": "MONDO:0002554", "names": ["sympathetic schwannoma", "Sympathetic Schwannoma", "Sympathetic Neurilemmoma", "sympathetic neurilemmoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sympathetic neurilemmoma", "shortest_name_length": 22}
{"curie": "UMLS:C1512479", "names": ["Hodgkin's Lymphoma (Antiquated)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's Lymphoma (Antiquated)", "shortest_name_length": 31}
{"curie": "MONDO:0011630", "names": ["RP28", "RP 28", "RETINITIS PIGMENTOSA 28", "retinitis pigmentosa 28", "FAM161A retinitis pigmentosa", "retinitis pigmentosa type 28", "retinitis pigmentosa caused by mutation in FAM161A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 28", "shortest_name_length": 4}
{"curie": "MONDO:0013315", "names": ["RP57", "retinitis pigmentosa 57", "RETINITIS PIGMENTOSA 57", "PDE6G retinitis pigmentosa", "retinitis pigmentosa type 57", "retinitis pigmentosa caused by mutation in PDE6G"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 57", "shortest_name_length": 4}
{"curie": "MONDO:0002478", "names": ["mixed germ cell-Sex Cord tumor", "Mixed Germ Cell-Sex Cord Tumor", "mixed germ cell-Sex cord tumor", "mixed germ cell-Sex cord neoplasm", "Mixed Germ Cell-Sex Cord Neoplasm", "mixed germ cell-sex cord neoplasm", "Mixed Germ Cell-Sex Cord-Stromal Tumor", "mixed germ cell-Sex cord-stromal tumor", "Mixed germ cell-sex cord-stromal tumor", "mixed germ cell-sex cord-stromal tumor", "Mixed germ cell-sex cord-stromal tumour", "Mixed Germ Cell-Sex Cord-Stromal Neoplasm", "mixed germ cell-Sex cord-stromal neoplasm", "mixed germ cell-sex cord-stromal tumor (morphologic abnormality)", "Mixed germ cell-sex cord-stromal tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed germ cell-sex cord-stromal tumor", "shortest_name_length": 30}
{"curie": "MONDO:0054836", "names": ["PKDYS2", "PARKINSONISM-DYSTONIA, INFANTILE, 2", "parkinsonism-dystonia, infantile, 2", "Parkinsonism-dystonia, infantile, 2", "PARKINSONISM-DYSTONIA 2, INFANTILE-ONSET"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parkinsonism-dystonia, infantile, 2", "shortest_name_length": 6}
{"curie": "MONDO:0011770", "names": ["AAT2", "FAA2", "aortic aneurysm, familial thoracic 2", "Aortic Aneurysm, Familial Thoracic 2", "AORTIC ANEURYSM, FAMILIAL THORACIC 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic aneurysm, familial thoracic 2", "shortest_name_length": 4}
{"curie": "UMLS:C4331314", "names": ["Stage I Hypopharyngeal Throat Cancer", "Stage I Hypopharyngeal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Hypopharyngeal Carcinoma AJCC v8", "shortest_name_length": 36}
{"curie": "MONDO:0021045", "names": ["Fibroepithelial Tumor", "Fibroepithelial tumor", "fibroepithelial tumor", "Fibroepithelial tumour", "Fibroepithelial Neoplasm", "Fibroepithelial neoplasm", "fibroepithelial neoplasm", "Neoplasm, Fibroepithelial", "FIBROEPITHELIAL NEOPLASMS", "Fibroepithelial Neoplasms", "Neoplasms, Fibroepithelial", "Fibroepithelial neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibroepithelial neoplasm", "shortest_name_length": 21}
{"curie": "UMLS:C5206570", "names": ["Refractory Intermediate Risk Acute Myeloid Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Intermediate Risk Acute Myeloid Leukemia", "shortest_name_length": 51}
{"curie": "MONDO:0014742", "names": ["PARK22", "Parkinson's disease 22", "CHCHD2 Parkinson disease", "Parkinson disease 22, autosomal dominant", "PARKINSON DISEASE 22, AUTOSOMAL DOMINANT", "autosomal dominant Parkinson's disease 22", "Parkinson disease caused by mutation in CHCHD2", "Parkinson disease 22, autosomal dominant; PARK22"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parkinson disease 22, autosomal dominant", "shortest_name_length": 6}
{"curie": "UMLS:C1336080", "names": ["Nipple Intraepidermal Squamous Carcinoma", "Squamous Cell Carcinoma In Situ of Nipple", "Intraepidermal Squamous Carcinoma of Nipple", "Squamous Cell Carcinoma In Situ of the Nipple", "Intraepidermal Squamous Carcinoma of the Nipple"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Squamous Cell Carcinoma In Situ of the Nipple", "shortest_name_length": 40}
{"curie": "UMLS:C4744388", "names": ["Sellar Yolk Sac Tumor", "Yolk Sac Tumor of the Sellar Region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sellar Yolk Sac Tumor", "shortest_name_length": 21}
{"curie": "MONDO:0030456", "names": ["LGMDR27", "muscular dystrophy, limb-girdle, autosomal recessive 27", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 27"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy, limb-girdle, autosomal recessive 27", "shortest_name_length": 7}
{"curie": "UMLS:C0685943", "names": ["Metastasis to the Lip", "Metastatic Tumor to the Lip", "Metastatic Neoplasm to the Lip", "lip neoplasm malignant secondary", "Secondary malignant neoplasm of lip", "Metastatic malignant neoplasm to lip", "Metastatic malignant neoplasm of lip", "Metastatic Malignant Neoplasm in the Lip", "Secondary malignant neoplasm of lip, NOS", "Metastatic Malignant Neoplasm to the Lip", "Metastatic malignant neoplasm to lip, NOS", "Secondary malignant neoplasm of lip (diagnosis)", "Metastatic malignant neoplasm to lip (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to lip", "shortest_name_length": 21}
{"curie": "MONDO:0012888", "names": ["SS2", "BTNL2 sarcoidosis", "susceptibility to sarcoidosis 2", "sarcoidosis, susceptibility to, 2", "SARCOIDOSIS, SUSCEPTIBILITY TO, 2", "sarcoidosis, susceptibility to, type 2", "sarcoidosis caused by mutation in BTNL2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sarcoidosis, susceptibility to, 2", "shortest_name_length": 3}
{"curie": "MONDO:0016783", "names": ["maternal 14q32.2 hypermethylation syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maternal 14q32.2 hypermethylation syndrome", "shortest_name_length": 42}
{"curie": "MONDO:0008924", "names": ["cataract and congenital ichthyosis", "CATARACT AND CONGENITAL ICHTHYOSIS", "Cataract and congenital ichthyosis", "congenital cataract-ichthyosis syndrome", "Syndromic cataract and congenital ichthyosis", "Syndermotic cataract and congenital ichthyosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital cataract-ichthyosis syndrome", "shortest_name_length": 34}
{"curie": "MONDO:0001166", "names": ["Nephritis", "NEPHRITIS", "nephritis", "Nephritides", "nephritis NOS", "Nephritis NOS", "Nephritis, NOS", "Renal inflammation", "kidney inflammation", "Kidney inflammation", "Nephritis (disorder)", "nephritis (diagnosis)", "inflammation of kidney", "Inflammation of kidney"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephritis", "shortest_name_length": 9}
{"curie": "MONDO:0012137", "names": ["CARNEY COMPLEX VARIANT", "Carney complex variant", "Carney Complex Variant", "CARNEY complex variant", "Carney complex - trismus - pseudocamptodactyly syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carney complex - trismus - pseudocamptodactyly syndrome", "shortest_name_length": 22}
{"curie": "MONDO:0018708", "names": ["OTSCC", "oral tongue squamous cell carcinoma", "squamous cell carcinoma of the oral tongue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "squamous cell carcinoma of the oral tongue", "shortest_name_length": 5}
{"curie": "MONDO:0018418", "names": ["SPG66", "autosomal recessive spastic paraplegia type 66"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive spastic paraplegia type 66", "shortest_name_length": 5}
{"curie": "UMLS:C1711165", "names": ["Low Grade Cartilaginous Component Present"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Grade Cartilaginous Component Present", "shortest_name_length": 41}
{"curie": "MONDO:0014702", "names": ["SPG9B", "AR-SPG9B", "hereditary spastic paraplegia 9B", "hereditary spastic paraplegia type 9B", "autosomal recessive spastic paraplegia 9B", "SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE", "spastic paraplegia 9B, autosomal recessive", "autosomal recessive spastic paraplegia type 9B", "Autosomal recessive spastic paraplegia type 9B", "autosomal recessive complex spastic paraplegia type 9B", "ALDH18A1 autosomal recessive complex spastic paraplegia", "Autosomal recessive spastic paraplegia type 9B (disorder)", "autosomal recessive spastic paraplegia type 9B (diagnosis)", "autosomal recessive complex spastic paraplegia caused by mutation in ALDH18A1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive complex spastic paraplegia type 9B", "shortest_name_length": 5}
{"curie": "MONDO:0004690", "names": ["tonsillar fossa cancer", "cancer of tonsillar fossa", "malignant tumor of tonsillar fossa", "malignant tonsillar fossa neoplasm", "Malignant tumor of tonsillar fossa", "Malignant tumour of tonsillar fossa", "malignant neoplasm of tonsillar fossa", "Malignant neoplasm of tonsillar fossa", "Malignant tumor of tonsillar fossa (disorder)", "malignant neoplasm of tonsillar fossa (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tonsillar fossa cancer", "shortest_name_length": 22}
{"curie": "UMLS:C1699561", "names": ["infection vulva", "Vulval Infection", "Vulval infection", "vulval infection", "vulval infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulval Infection", "shortest_name_length": 15}
{"curie": "UMLS:C2046622", "names": ["Hodgkin's lymphoma of CNS", "Hodgkin's lymphoma of CNS (diagnosis)", "Central Nervous System Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's lymphoma of CNS", "shortest_name_length": 25}
{"curie": "MONDO:0007862", "names": ["WS3", "Klein Syndrome", "Klein syndrome", "Kleins Syndrome", "Syndrome, Klein", "Klein's Syndrome", "Syndrome, Klein's", "Klein-Waardenberg syndrome", "Klein Waardenburg Syndrome", "Waardenburg Klein Syndrome", "Klein Waardenburg syndrome", "Klein-Waardenburg Syndrome", "Klein-Waardenburg syndrome", "KLEIN-WAARDENBURG SYNDROME", "Waardenburg-Klein Syndrome", "Waardenburg syndrome type 3", "Syndrome, Waardenburg-Klein", "Syndrome, Klein-Waardenburg", "Waardenburg Syndrome Type 3", "Waardenburg syndrome, type 3", "Waardenburg Syndrome, Type 3", "WAARDENBURG SYNDROME, TYPE 3", "Klein-Waardenberg's syndrome", "Waardenburg syndrome type III", "WAARDENBURG SYNDROME, TYPE III", "Waardenburg Syndrome, Type III", "Waardenburg syndrome type 3 (disorder)", "Waardenburg syndrome with limb anomalies", "Waardenburg syndrome type III (diagnosis)", "Waardenburg syndrome with upper limb anomalies", "WAARDENBURG SYNDROME WITH UPPER LIMB ANOMALIES", "Waardenburg Syndrome with Upper Limb Anomalies", "White forelock (poliosis) syndrome with multiple congenital malformations", "White Forelock (Poliosis) Syndrome with Multiple Congenital Malformations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Waardenburg syndrome type 3", "shortest_name_length": 3}
{"curie": "MONDO:0014331", "names": ["MYMY6", "moyamoya 6 with achalasia", "Moyamoya disease 6 with achalasia", "Moyamoya disease with early onset achalasia", "Moyamoya disease with early-onset achalasia", "MOYAMOYA DISEASE 6 WITH OR WITHOUT ACHALASIA", "Moyamoya disease with early onset achalasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Moyamoya disease with early-onset achalasia", "shortest_name_length": 5}
{"curie": "MONDO:0002920", "names": ["Malignant Brenner tumor", "Malignant Brenner Tumor", "Brenner tumor, malignant", "Malignant Brenner tumour", "Brenner Tumor, Malignant", "tumor; Brenner, malignant", "Brenner tumour, malignant", "Brenner; tumor, malignant", "Malignant Ovarian Brenner Tumor", "malignant ovarian Brenner tumor", "ovarian Brenner tumor, malignant", "malignant Brenner tumor of ovary", "Malignant Brenner Tumor of Ovary", "malignant Brenner tumor of the ovary", "Malignant Brenner Tumor of the Ovary", "Malignant Ovarian Transitional Cell Tumor", "Malignant Ovarian Transitional Cell Neoplasm", "malignant Brenner tumor of ovary (diagnosis)", "Brenner tumor, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant ovarian Brenner tumor", "shortest_name_length": 23}
{"curie": "UMLS:C5418786", "names": ["Advanced Rectal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Rectal Carcinoma", "shortest_name_length": 25}
{"curie": "UMLS:C0263358", "names": ["Erythema gyratum perstans", "Erythema figuratum perstans", "erythema; figuratum perstans", "figuratum perstans; erythema", "annulare centrifugum erythema", "Erythema annulare centrifugum", "erythema annulare centrifugum", "Darier; erythema annulare centrifugum", "erythema; annulare centrifugum, Darier", "Erythema annulare centrifugum (disorder)", "erythema annulare centrifugum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Erythema annulare centrifugum", "shortest_name_length": 25}
{"curie": "MONDO:0001556", "names": ["occlusion; urethra", "urethra; occlusion", "urethra obstruction", "Urethral Obstruction", "urethral obstruction", "Urethral obstruction", "URETHRAL OBSTRUCTION", "urethra; obstruction", "obstruction; urethra", "Obstruction, Urethral", "Urethral Obstructions", "obstruction of urethra", "Obstruction of urethra", "Obstructions, Urethral", "Urethral obstruction, NOS", "Obstruction of urethra, NOS", "urethral obstruction (disease)", "urethral obstruction (diagnosis)", "Obstruction of urethra (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urethral obstruction", "shortest_name_length": 18}
{"curie": "MONDO:0006268", "names": ["Liver Diffuse Large B-Cell Lymphoma", "liver diffuse large B-cell lymphoma", "Hepatic Diffuse Large B-Cell Lymphoma", "hepatic diffuse large B-cell lymphoma", "diffuse large B-cell lymphoma of liver", "large B-cell diffuse lymphoma of liver", "Primary Liver Diffuse Large B-Cell Lymphoma", "primary liver diffuse large B-cell lymphoma", "primary hepatic diffuse large B-cell lymphoma", "Primary Hepatic Diffuse Large B-Cell Lymphoma", "large B-cell diffuse lymphoma of liver (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "liver diffuse large B-cell lymphoma", "shortest_name_length": 35}
{"curie": "MONDO:0000683", "names": ["Topographical agnosia", "topographical agnosia", "Topographical Agnosia", "Topographical Agnosias", "Agnosia, Topographical", "Agnosias, Topographical", "visual disorientation syndrome", "Visual disorientation syndrome", "Visual Disorientation Syndrome", "Visual Disorientation Syndromes", "Syndrome, Visual Disorientation", "Syndromes, Visual Disorientation", "Topographical agnosia (disorder)", "visual disorientation syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "topographical agnosia", "shortest_name_length": 21}
{"curie": "UMLS:C4053766", "names": ["Rhizomelic Dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rhizomelic Dysplasia", "shortest_name_length": 20}
{"curie": "MONDO:0002775", "names": ["ANOVULATION", "Anovulation", "anovulation", "Anovulations", "ovulation absent", "Ovulation absent", "absent ovulation", "OVULATION FAILURE", "ovulation failure", "Ovulation failure", "ovulation; failure", "failure; ovulation", "Anovulation (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anovulation", "shortest_name_length": 11}
{"curie": "MONDO:0003208", "names": ["SBC", "JSCB", "secretory carcinoma", "Secretory Carcinoma", "juvenile breast carcinoma", "Juvenile Breast Carcinoma", "Breast Secretory Carcinoma", "breast secretory carcinoma", "Secretory Breast Carcinoma", "secretory breast carcinoma", "Secretory breast carcinoma", "Juvenile carcinoma of breast", "juvenile carcinoma of breast", "Juvenile Carcinoma of Breast", "secretory carcinoma of breast", "Secretory carcinoma of breast", "Secretory Carcinoma of Breast", "juvenile carcinoma (formerly)", "Cystic hypersecretory carcinoma", "juvenile carcinoma of the breast", "Juvenile Carcinoma of the Breast", "Juvenile carcinoma of the breast", "secretory carcinoma of the breast", "Secretory Carcinoma of the Breast", "Secretory carcinoma of the breast", "juvenile secretory breast carcinoma", "Juvenile Secretory Breast Carcinoma", "cystic hypersecretory breast carcinoma", "Juvenile Secretory carcinoma of breast", "juvenile secretory carcinoma of breast", "Juvenile Secretory Carcinoma of Breast", "Cystic Hypersecretory Breast Carcinoma", "secretory carcinoma of breast (diagnosis)", "cystic hypersecretory carcinoma of breast", "hypersecretory cystic carcinoma of breast", "Cystic Hypersecretory Carcinoma of Breast", "juvenile secretory carcinoma of the breast", "Juvenile Secretory Carcinoma of the Breast", "cystic hypersecretory carcinoma of the breast", "Cystic Hypersecretory Carcinoma of the Breast", "Invasive Cystic Hypersecretory Duct Breast Carcinoma", "invasive cystic hypersecretory duct breast carcinoma", "hypersecretory cystic carcinoma of breast (diagnosis)", "Infiltrating Cystic Hypersecretory Duct Breast Carcinoma", "infiltrating cystic hypersecretory duct breast carcinoma", "Juvenile carcinoma of the breast (morphologic abnormality)", "juvenile carcinoma of the breast (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast secretory carcinoma", "shortest_name_length": 3}
{"curie": "MONDO:0005721", "names": ["coxsackievirus", "virus coxsackie", "COXSACKIE VIRUS", "Coxsackie virus", "coxsackie virus", "disease coxsackie", "coxsackie disease", "coxsackie viral disease", "disease coxsackie virus", "Coxsackie virus disease", "Coxsackievirus Infection", "coxsackievirus infection", "coxsackievirus infections", "Coxsackie Virus Infection", "coxsackie viral infection", "infections coxsackievirus", "Coxsackie viral infection", "Coxsackievirus infections", "coxsackie virus infection", "Coxsackievirus Infections", "Coxsackie viral infections", "coxsackie virus infections", "coxsackie viral infections", "Coxsackie Virus Infections", "Infections, Coxsackievirus", "Infections, Coxsackie Virus", "Coxsackievirus infection NOS", "coxsackievirus infectious disease", "viral; infection, coxsackie(virus)", "Coxsackie virus disease (disorder)", "infection; viral, coxsackie(virus)", "coxsackie viral disease (diagnosis)", "viral; infection, coxsackie(virus), unspecified nature or site", "infection; viral, coxsackie(virus), unspecified nature or site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coxsackievirus infectious disease", "shortest_name_length": 14}
{"curie": "MONDO:0016908", "names": ["partial deletion of chromosome 9q", "partial monosomy of chromosome 9q", "partial deletion of the long arm of chromosome 9", "partial monosomy of the long arm of chromosome 9", "partial monosomy of the long arm of chromosome type 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial monosomy of the long arm of chromosome 9", "shortest_name_length": 33}
{"curie": "UMLS:C1096721", "names": ["Neonatal Late-Onset Sepsis", "Neonatal Late-Onset Sepses", "Neonatal Late Onset Sepsis", "Late onset neonatal sepsis", "Late-Onset Neonatal Sepsis", "Late-onset neonatal sepsis", "Late-Onset Sepsis, Neonatal", "Sepses, Neonatal Late-Onset", "Neonatal Sepsis, Late-Onset", "Sepsis, Neonatal Late-Onset", "Late-Onset Sepses, Neonatal", "septicemia of newborn late-onset", "Late-onset neonatal sepsis (disorder)", "Late-onset neonatal sepsis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neonatal Late-Onset Sepsis", "shortest_name_length": 26}
{"curie": "MONDO:0005504", "names": ["DIPHTERIA", "Diphtheria", "diphtheria", "DIPHTHERIA", "Diphtheria, NOS", "Corynebacteriosis", "diphtheria (diagnosis)", "infection; diphtherial", "diphtherial; infection", "Diphtheria, unspecified", "Corynebacteria infections", "Corynebacterium infection", "Corynebacterium Infection", "corynebacterium infection", "Corynebacterium Infections", "Infection, Corynebacterium", "Infections, Corynebacterium", "Corynebacterium infection NOS", "Infection due to Corynebacterium", "Infection caused by Corynebacterium", "Corynebacterium diphtheriae infection", "Corynebacterium diphtheriae Infection", "Infection, Corynebacterium diphtheriae", "Corynebacterium diphtheriae Infections", "Corynebacterium diphtheriae; infection", "infection; Corynebacterium diphtheriae", "Infection due to Corynebacterium diphtheriae", "Diphtheria due to Corynebacterium diphtheriae", "Infection caused by Corynebacterium (disorder)", "Infection caused by Corynebacterium diphtheriae", "Diphtheria caused by Corynebacterium diphtheriae", "Infection caused by Corynebacterium diphtheriae (disorder)", "Diphtheria caused by Corynebacterium diphtheriae (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diphtheria", "shortest_name_length": 9}
{"curie": "MONDO:0011373", "names": ["urinary tract infections, recurrent, susceptibility to", "URINARY TRACT INFECTIONS, RECURRENT, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urinary tract infections, recurrent, susceptibility to", "shortest_name_length": 54}
{"curie": "MONDO:0005314", "names": ["RRMS", "Relapsing-remitting MS", "Remitting Relapsing Multiple Sclerosis", "relapsing-remitting multiple sclerosis", "Relapsing remitting multiple sclerosis", "Relapsing Remitting Multiple Sclerosis", "multiple relapsing remitting sclerosis", "Relapsing-remitting multiple sclerosis", "Relapsing-Remitting Multiple Sclerosis", "Remitting-Relapsing Multiple Sclerosis", "Multiple Sclerosis, Remitting-Relapsing", "Multiple Sclerosis, Relapsing-Remitting", "Multiple Sclerosis, Relapsing Remitting", "Multiple sclerosis (MS) relapsing remitting", "Relapsing remitting multiple sclerosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "relapsing-remitting multiple sclerosis", "shortest_name_length": 4}
{"curie": "UMLS:C0684984", "names": ["Metastatic Tumor to the Larynx", "Metastatic Neoplasm to the Larynx", "Secondary malignant neoplasm of larynx", "laryngeal malignant neoplasm secondary", "Metastatic malignant neoplasm to larynx", "Metastatic malignant neoplasm of larynx", "Metastatic Malignant Neoplasm in the Larynx", "Metastatic Malignant Neoplasm to the Larynx", "Secondary malignant neoplasm of larynx, NOS", "Metastatic malignant neoplasm to larynx, NOS", "Secondary malignant neoplasm of larynx (diagnosis)", "Metastatic malignant neoplasm to larynx (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to larynx", "shortest_name_length": 30}
{"curie": "UMLS:C4528737", "names": ["Stage IV Vulvar Cancer", "Stage IV Vulvar Cancer AJCC v8", "Stage IV Vulvar Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Vulvar Cancer AJCC v8", "shortest_name_length": 22}
{"curie": "MONDO:0016166", "names": ["genetic hyperparathyroidism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genetic hyperparathyroidism", "shortest_name_length": 27}
{"curie": "MONDO:0007909", "names": ["FML", "LIPO", "LIPOMA", "lipoma", "Multiple Lipomatoses", "Multiple Lipomatosis", "LIPOMATOSIS, MULTIPLE", "lipomatosis, multiple", "Lipomatosis, Multiple", "Lipomatoses, Multiple", "Familial Multiple Lipoma", "Familial Multiple Lipomas", "Multiple Lipoma, Familial", "Familial multiple lipomata", "Multiple Lipomas, Familial", "familial multiple lipomatosis", "Familial Multiple Lipomatosis", "Familial Multiple Lipomatoses", "Familial multiple lipomatosis", "LIPOMATOSIS, FAMILIAL MULTIPLE", "Lipomatoses, Familial Multiple", "lipomatosis, familial multiple", "Lipomatosis, Familial Multiple", "Familial multiple lipomata (disorder)", "Familial multiple lipomatosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial multiple lipomatosis", "shortest_name_length": 3}
{"curie": "UMLS:C1518741", "names": ["Ovarian Stromal-Leydig Tumor", "Ovarian Stromal-Leydig Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Stromal-Leydig Cell Tumor", "shortest_name_length": 28}
{"curie": "UMLS:C0520547", "names": ["Poor peripheral circulation", "Poor peripheral circulation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Poor peripheral circulation", "shortest_name_length": 27}
{"curie": "UMLS:C0279564", "names": ["Invasive Breast Lobular Carcinoma with Predominant In Situ Component", "lobular invasive breast carcinoma with predominant in situ component", "Invasive Lobular Breast Carcinoma with Predominant In Situ Component", "invasive lobular breast carcinoma with predominant in situ component", "Infiltrating Lobular Breast Carcinoma with Predominant In Situ Component"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Invasive Breast Lobular Carcinoma with Predominant In Situ Component", "shortest_name_length": 68}
{"curie": "UMLS:C5419900", "names": ["Esophageal Soft Tissue Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Soft Tissue Neoplasm", "shortest_name_length": 31}
{"curie": "UMLS:C1333268", "names": ["Deep Penetrating Nevus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Deep Penetrating Nevus", "shortest_name_length": 22}
{"curie": "MONDO:0012132", "names": ["CRCS1", "GALNT12 colorectal cancer", "susceptibility to colorectal cancer 1", "COLORECTAL CANCER, SUSCEPTIBILITY TO, 1", "colorectal cancer, susceptibility to, 1", "colorectal cancer, susceptibility to, type 1", "colorectal cancer caused by mutation in GALNT12", "COLORECTAL ADENOMA AND CANCER, SUSCEPTIBILITY TO", "colorectal adenoma and cancer, susceptibility to", "COLORECTAL CANCER, SUSCEPTIBILITY TO, ON CHROMOSOME 9", "colorectal cancer, susceptibility to, on chromosome 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorectal cancer, susceptibility to, 1", "shortest_name_length": 5}
{"curie": "UMLS:C0266452", "names": ["hemicephaly", "Hemicephaly", "Hemicephalia", "hemicephalus", "Hemicephalus", "hemicephalia", "Hemicephaly (disorder)", "Congenital absence of cerebrum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemicephaly", "shortest_name_length": 11}
{"curie": "UMLS:C0000932", "names": ["traffic crash", "traffic accident", "Traffic accident", "Traffic Accident", "Traffic accidents", "Accident, Traffic", "Traffic Accidents", "traffic accidents", "Accidents, Traffic", "automobile accident", "automobile accidents", "motor vehicle accident", "motor vehicle accidents", "motor vehicle collision"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Traffic accidents", "shortest_name_length": 13}
{"curie": "MONDO:0014052", "names": ["CMS8", "CMSPPD", "congenital myasthenic syndrome 8", "myasthenic syndrome, congenital, 8", "MYASTHENIC SYNDROME, CONGENITAL, 8", "AGRN congenital myasthenic syndrome", "congenital myasthenic syndrome type 8", "myasthenic syndrome, congenital, type 8", "congenital myasthenic syndrome due to agrin deficiency", "MYASTHENIC SYNDROME, CONGENITAL, DUE TO AGRIN DEFICIENCY", "myasthenic syndrome, congenital, due to agrin deficiency", "congenital myasthenic syndrome caused by mutation in AGRN", "congenital myasthenic syndrome 8 with pre- and postsynaptic defects", "myasthenic syndrome, congenital, with Pre- and postsynaptic defects", "MYASTHENIC SYNDROME, CONGENITAL, WITH PRE- AND POSTSYNAPTIC DEFECTS", "myasthenic syndrome, congenital, 8, with pre- and postsynaptic defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myasthenic syndrome 8", "shortest_name_length": 4}
{"curie": "MONDO:0032599", "names": ["IMD15A", "immunodeficiency 15a", "IMMUNODEFICIENCY 15A", "immunodeficiency 15A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 15a", "shortest_name_length": 6}
{"curie": "UMLS:C5557380", "names": ["Vulvar Smooth Muscle Tumor of Uncertain Malignant Potential", "Vulvar Smooth Muscle Neoplasm of Uncertain Malignant Potential"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Smooth Muscle Tumor of Uncertain Malignant Potential", "shortest_name_length": 59}
{"curie": "MONDO:0004911", "names": ["CV syphilis", "Cardiovascular Syphilis", "Cardiovascular syphilis", "CARDIOVASCULAR SYPHILIS", "cardiovascular syphilis", "Syphilis, cardiovascular", "Syphilis, Cardiovascular", "Cardiovascular syphilis NOS", "Cardiovascular syphilis, NOS", "Cardiovascular syphilis (disorder)", "cardiovascular syphilis (diagnosis)", "syphilis; cardiovascular (etiology)", "Cardiovascular syphilis, unspecified", "cardiovascular; syphilitic (etiology)", "Other specified cardiovascular syphilis", "syphilis; cardiovascular (manifestation)", "cardiovascular; syphilitic (manifestation)", "disease (or disorder); heart, syphilitic (etiology)", "disease (or disorder); heart, syphilitic (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiovascular syphilis", "shortest_name_length": 11}
{"curie": "UMLS:C2314994", "names": ["spinal; infarction", "infarction; spinal", "Spinal cord infarct", "SPINAL CORD INFARCTION", "Spinal Cord Infarction", "cord infarction spinal", "Spinal cord infarction", "spinal cord infarction", "Infarction of spinal cord", "Infarction of Spinal Cord", "spinal cord infarction (diagnosis)", "Infarction of spinal cord (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infarction of spinal cord", "shortest_name_length": 18}
{"curie": "MONDO:0017232", "names": ["IDMDC", "recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0009063", "names": ["VMCKD", "ventriculomegaly-cystic kidney disease", "Ventriculomegaly-cystic kidney disease", "ventriculomegaly - cystic kidney disease", "ventriculomegaly with cystic kidney disease", "VENTRICULOMEGALY WITH CYSTIC KIDNEY DISEASE", "cystic kidney disease with ventriculomegaly", "Cystic Kidney Disease with Ventriculomegaly", "Cerebral ventriculomegaly, cystic kidney disease", "VMCKD - ventriculomegaly with cystic kidney disease", "congenital nephrosis-cerebral ventriculomegaly syndrome", "Congenital nephrosis-cerebral ventriculomegaly syndrome", "Congenital nephrosis, cerebral ventriculomegaly syndrome", "Cerebral ventriculomegaly, cystic kidney disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ventriculomegaly-cystic kidney disease", "shortest_name_length": 5}
{"curie": "UMLS:C0853254", "names": ["Nasal passage irritation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasal passage irritation", "shortest_name_length": 24}
{"curie": "UMLS:C4524632", "names": ["Esophageal Adenocarcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Adenocarcinoma by AJCC v8 Stage", "shortest_name_length": 42}
{"curie": "MONDO:0002342", "names": ["chondropathy", "Chondropathy", "chondromalacia", "Chondromalacia", "Chondropathies", "CHONDROMALACIA", "Chondromalacias", "Chondropathy NOS", "cartilage disease", "Cartilage Disease", "Chondromalacia NOS", "Cartilage disorder", "cartilage disorder", "cartilage diseases", "Cartilage Diseases", "Chondromalacia, NOS", "Cartilage disorders", "Cartilage Disorders", "Cartilage--Diseases", "cartilage disorders", "Disease of cartilage", "disorder of cartilage", "Disorder of cartilage", "Cartilage disorder NOS", "Chondropathies (M91-M94)", "joint cartilage softening", "Chondromalacia (disorder)", "chondromalacia (diagnosis)", "Cartilage disorder (disorder)", "Functional cartilage disorder", "Cartilage disorder, functional", "Chondromalacia, site unspecified", "disease (or disorder); cartilage", "Chondromalacia, unspecified site", "Unspecified disorder of cartilage", "disorder of cartilage (diagnosis)", "Disorder of cartilage, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chondromalacia", "shortest_name_length": 12}
{"curie": "MONDO:0009426", "names": ["HRD", "SSS", "HRDS", "HRD syndrome", "Sanjad Sakati syndrome", "Sanjad-Sakati syndrome", "Sanjad-Sakati Syndrome", "SANJAD-SAKATI SYNDROME", "Richardson-Kirk syndrome", "Richardson Kirk syndrome", "SSS - Sanjad Sakati syndrome", "Sanjad Sakati syndrome (disorder)", "HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME", "Hypoparathyroidism-retardation-dysmorphism syndrome", "hypoparathyroidism-retardation-dysmorphism syndrome", "Hypoparathyroidism-Retardation-Dysmorphism Syndrome", "Hypoparathyroidism-intellectual disability-dysmorphism syndrome", "hypoparathyroidism-intellectual disability-dysmorphism syndrome", "Hypoparathyroidism, intellectual disability, dysmorphism syndrome", "hypoparathyroidism with short stature, mental retardation and seizures", "HYPOPARATHYROIDISM WITH SHORT STATURE, MENTAL RETARDATION, AND SEIZURES", "hypoparathyroidism with short stature, mental retardation, and seizures", "Hypoparathyroidism with Short Stature, Mental Retardation, and Seizures", "Hypoparathyroidism with short stature, mental retardation, and seizures", "hypoparathyroidism-short stature-intellectual disability-seizures syndrome", "Hypoparathyroidism-short stature-intellectual disability-seizures syndrome", "HYPOPARATHYROIDISM-INTELLECTUAL DEVELOPMENTAL DISORDER-DYSMORPHISM SYNDROME", "hypoparathyroidism with short stature, intellectual disability and seizures", "hypoparathyroidism with short stature, intellectual disability, and seizures", "Hypoparathyroidism, short stature, intellectual disability, seizures syndrome", "hypoparathyroidism, congenital, associated with dysmorphism, growth retardation and developmental delay", "HYPOPARATHYROIDISM, CONGENITAL, ASSOCIATED WITH DYSMORPHISM, GROWTH RETARDATION, AND DEVELOPMENTAL DELAY", "Hypoparathyroidism, Congenital, Associated with Dysmorphism, Growth Retardation, and Developmental Delay", "hypoparathyroidism, congenital, associated with Dysmorphism, Growth retardation, and developmental delay"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypoparathyroidism-retardation-dysmorphism syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C1335319", "names": ["Panniculitis Ossificans"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Panniculitis Ossificans", "shortest_name_length": 23}
{"curie": "UMLS:C1850597", "names": ["Leigh Syndrome Due To Mitochondrial Complex II Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leigh Syndrome Due To Mitochondrial Complex II Deficiency", "shortest_name_length": 57}
{"curie": "MONDO:0010728", "names": ["SCARF SYNDROME", "SCARF syndrome", "Skeletal Abnormalities, Cutis Laxa, Craniostenosis, Ambiguous Genitalia, Retardation, And Facial Abnormalities", "skeletal abnormalities, cutis laxa, craniostenosis, ambiguous genitalia, retardation, and Facial abnormalities", "SKELETAL ABNORMALITIES, CUTIS LAXA, CRANIOSTENOSIS, AMBIGUOUS GENITALIA, RETARDATION, AND FACIAL ABNORMALITIES", "Skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality syndrome", "SCARF (skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality) syndrome", "Skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality syndrome (disorder)", "Skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SCARF syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0044687", "names": ["CRION", "chronic recurrent isolated optic neuritis", "chronic relapsing inflammatory optic neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic relapsing inflammatory optic neuropathy", "shortest_name_length": 5}
{"curie": "MONDO:0021224", "names": ["iris tumor", "Iris Tumor", "iris tumors", "Iris Neoplasm", "Iris neoplasm", "Tumor of iris", "iris neoplasm", "Tumor of Iris", "tumor of iris", "Iris Neoplasms", "Neoplasm, Iris", "Tumour of iris", "iris neoplasms", "Neoplasms, Iris", "neoplasm of iris", "Neoplasm of Iris", "Tumor of the Iris", "tumor of the iris", "Neoplasm of the Iris", "neoplasm of the iris", "iris neoplasm (disease)", "Tumor of iris (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "iris neoplasm", "shortest_name_length": 10}
{"curie": "UMLS:C3472607", "names": ["Pancreatobiliary-type carcinoma", "Adenocarcinoma, pancreatobiliary-type", "Ampulla of Vater Pancreatobiliary Type Adenocarcinoma", "Pancreatobiliary-type carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatobiliary-type carcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C5553945", "names": ["Recurrent Gliomatosis Cerebri"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Gliomatosis Cerebri", "shortest_name_length": 29}
{"curie": "MONDO:0005842", "names": ["antritis", "maxillary sinusitis", "Maxillary sinusitis", "MAXILLARY SINUSITIS", "sinusitis maxillary", "Maxillary Sinusitis", "Sinusitis, Maxillary", "sinusitis; maxillary", "maxillary; sinusitis", "Maxillary Sinusitides", "Sinusitides, Maxillary", "Maxillary sinusitis NOS", "Maxillary sinusitis, NOS", "Maxillary sinusitis (disorder)", "Maxillary sinusitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maxillary sinusitis", "shortest_name_length": 8}
{"curie": "MONDO:0005707", "names": ["Coccidioses", "Coccidiosis", "COCCIDIOSIS", "coccidiosis", "Coccidiosis, NOS", "Coccidiosis infection", "intestinal coccidiosis", "Coccidiosis (disorder)", "Coccidiosis (diagnosis)", "coccidiosis (& [intestinal])", "protozoal disease coccidiosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coccidiosis", "shortest_name_length": 11}
{"curie": "MONDO:0006698", "names": ["cholelith", "gallstone", "Gallstone", "Gallstones", "GS - Gallstone", "Gallbladder stone", "Gallbladder Stone", "Gallbladder stones", "cholecystolithiasis", "Cholecystolithiasis", "GALL BLADDER STONES", "CALCULUS GALLBLADDER", "Gallbladder calculus", "Gallbladder Calculus", "Calculus gallbladder", "Stone in gallbladder", "calculus; gallbladder", "gallbladder; calculus", "GALLBLADDER, CALCULUS", "Calculus in gallbladder", "calculus of gallbladder", "Calculus of gallbladder", "Gallbladder calculus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholecystolithiasis", "shortest_name_length": 9}
{"curie": "MONDO:0006313", "names": ["Nabothian Cyst", "Nabothian cyst", "NABOTHIAN CYST", "cyst nabothian", "nabothian cyst", "cyst; nabothian", "nabothian; cyst", "cysts nabothian", "Naboth follicles", "Nabothian follicle", "nabothian follicle", "naboth's follicles", "Naboth's follicles", "nabothian follicles", "FOLLICLE, NABOTHIAN", "nabothian; follicle", "follicle; nabothian", "Nabothian follicles", "nabothian gland cyst", "Nabothian gland cyst", "Nabothian cyst of cervix", "Nabothians follicle cyst", "Cyst;Nabothian(follicle)", "nabothian cyst (diagnosis)", "Nabothian cyst or follicle", "follicular; cyst, nabothian", "cyst; follicular, nabothian", "follicle; cervix (nabothian)", "Nabothian follicles on cervix", "Nabothian gland cyst or follicle", "cyst; cervix, nabothian follicle", "cervix; cyst, nabothian follicle", "nabothian cyst (physical finding)", "Mucous retention cyst of cervix uteri", "Mucous retention cyst of cervix uteri (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nabothian cyst", "shortest_name_length": 14}
{"curie": "MONDO:0011492", "names": ["Mandibulofacial Dysostosis Syndrome, Bauru Type", "MANDIBULOFACIAL DYSOSTOSIS SYNDROME, BAURU TYPE", "mandibulofacial dysostosis syndrome, Bauru type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mandibulofacial dysostosis syndrome, Bauru type", "shortest_name_length": 47}
{"curie": "MONDO:0001820", "names": ["focal labyrinthitis", "Focal labyrinthitis", "labyrinthitis circumscribed", "Circumscribed labyrinthitis", "circumscribed labyrinthitis", "LABYRINTHITIS, CIRCUMSCRIBED", "Circumscribed labyrinthitis (disorder)", "circumscribed labyrinthitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal labyrinthitis", "shortest_name_length": 19}
{"curie": "MONDO:0004297", "names": ["Lymphoepithelial Thymus Cancer", "lymphoepithelial Thymus cancer", "Thymic Lymphoepithelial Carcinoma", "lymphoepithelial cancer of Thymus", "Lymphoepithelial Cancer of Thymus", "malignant lymphoepithelial thymoma", "Malignant Lymphoepithelial Thymoma", "Lymphoepithelial malignant thymoma", "Lymphoepithelial Cancer of the Thymus", "lymphoepithelial cancer of the Thymus", "lymphoepithelioma-like thymic carcinoma", "Thymic Lymphoepithelioma-Like Carcinoma", "thymic lymphoepithelioma-like carcinoma", "lymphoepithelioma-like Thymus carcinoma", "Lymphoepithelioma-like Thymus Carcinoma", "Lymphoepithelioma-like Thymic Carcinoma", "lymphoepithelioma-like carcinoma of Thymus", "Lymphoepithelioma-like Carcinoma of Thymus", "lymphoepithelioma-like carcinoma of the Thymus", "Lymphoepithelioma-like carcinoma of the Thymus", "Lymphoepithelioma-like Carcinoma of the Thymus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphoepithelioma-like thymic carcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0012723", "names": ["LCA10", "Leber Congenital Amaurosis 10", "LEBER CONGENITAL AMAUROSIS 10", "Leber congenital amaurosis 10", "CEP290 Leber congenital amaurosis", "Leber congenital amaurosis type 10", "amaurosis congenita of Leber, type 10", "LEBER CONGENITAL AMAUROSIS 10 (disorder)", "Leber congenital amaurosis caused by mutation in CEP290"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leber congenital amaurosis 10", "shortest_name_length": 5}
{"curie": "MONDO:0018658", "names": ["dup(19)(p13.13)", "19p13.3 microduplication syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "19p13.3 microduplication syndrome", "shortest_name_length": 15}
{"curie": "UMLS:C1512439", "names": ["High Grade Prostatic Intraepithelial Neoplasia, Small Cell Neuroendocrine Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Prostatic Intraepithelial Neoplasia, Small Cell Neuroendocrine Variant", "shortest_name_length": 81}
{"curie": "UMLS:C5238932", "names": ["Locally Advanced Thyroid Gland Medullary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Thyroid Gland Medullary Carcinoma", "shortest_name_length": 50}
{"curie": "MONDO:0008882", "names": ["Congenital bowing of long bone", "congenital bowing of long bones", "bowing of long bones congenital", "Congenital bowing of long bones", "Congenital bowing of long bone (disorder)", "bowing of long bones, asymmetric and symmetric", "BOWING OF LONG BONES, ASYMMETRIC AND SYMMETRIC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital bowing of long bones", "shortest_name_length": 30}
{"curie": "UMLS:C1632842", "names": ["Complicated appendicitis", "complicated appendicitis", "Complicated appendicitis (disorder)", "complicated appendicitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Complicated appendicitis", "shortest_name_length": 24}
{"curie": "MONDO:0003175", "names": ["Cylindroma", "adenoid cystic cancer", "cylindroma (morphologic abnormality)", "salivary gland adenoid cystic cancer", "Salivary Gland Adenoid Cystic Cancer", "salivary gland adenoid cystic carcinoma", "Salivary Gland Adenoid Cystic Carcinoma", "adenoid cystic carcinoma, salivary gland", "Adenoid Cystic Carcinoma of Salivary Gland", "Adenoid cystic carcinoma of salivary gland", "adenoid cystic carcinoma of salivary gland", "Adenoid Cystic Carcinoma of the Salivary Gland", "adenoid cystic carcinoma of the salivary gland", "saliva-secreting gland adenoid cystic carcinoma", "adenoid cystic carcinoma (morphologic abnormality)", "Adenoid cystic carcinoma of salivary gland (disorder)", "adenoid cystic carcinoma of salivary gland (diagnosis)", "cancer of the salivary gland, adenoid cystic carcinoma", "carcinoma of the salivary gland, adenoid cystic carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "salivary gland adenoid cystic carcinoma", "shortest_name_length": 10}
{"curie": "MONDO:0019228", "names": ["histidine metabolism disease", "histidine; metabolic disorder", "metabolic disorder; histidine", "disorder of histidine metabolism", "Disorder of histidine metabolism", "Disorders of histidine metabolism", "histidine metabolism disturbances", "histidine metabolic process disease", "disturbance of histidine metabolism", "Disturbances of histidine metabolism", "inborn error of histidine metabolism", "Disorder of histidine metabolism, NOS", "inborn disorder of histidine metabolism", "disorder of histidine metabolic process", "inborn histidine metabolic process disorder", "Disorder of histidine metabolism (disorder)", "inborn error of histidine metabolic process", "histidine metabolism disturbances (diagnosis)", "Disorders of histidine metabolism, unspecified", "rare inborn error of histidine metabolic process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of histidine metabolism", "shortest_name_length": 28}
{"curie": "UMLS:C0333869", "names": ["Squamous cell atypia", "Squamous Cell Atypia", "Atypia, squamous cell", "Squamous cell atypia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Squamous cell atypia", "shortest_name_length": 20}
{"curie": "MONDO:0008496", "names": ["STORM SYNDROME", "storm syndrome", "Storm Syndrome", "pleiotropic, autosomal dominant disorder affecting connective tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "storm syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0014297", "names": ["JBTS22", "JOUBERT SYNDROME 22", "Joubert syndrome 22", "PDE6D Joubert syndrome", "Joubert syndrome type 22", "Joubert syndrome caused by mutation in PDE6D"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome 22", "shortest_name_length": 6}
{"curie": "MONDO:0017504", "names": ["apodia, unilateral", "congenital absence of foot, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "apodia, unilateral", "shortest_name_length": 18}
{"curie": "UMLS:C0854840", "names": ["Angioimmunoblastic T-Cell Lymphoma Stage II", "Stage II Angioimmunoblastic T-Cell Lymphoma", "Angioimmunoblastic T-cell lymphoma stage II", "Ann Arbor Stage II Angioimmunoblastic T-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Angioimmunoblastic T-cell lymphoma stage II", "shortest_name_length": 43}
{"curie": "MONDO:0042602", "names": ["Samson-Viljoen syndrome", "Samson Viljoen syndrome", "lateral facial cleft, cleft lip and palate, anophthalmia, microtia, clavicular agenesis and asternia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Samson-Viljoen syndrome", "shortest_name_length": 23}
{"curie": "UMLS:C1516061", "names": ["B1", "Astler-Coller B1 Rectal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Astler-Coller B1 Rectal Carcinoma", "shortest_name_length": 2}
{"curie": "UMLS:C5556344", "names": ["Unresectable Colon Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Colon Carcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0005316", "names": ["BV", "gardnerella", "bacterial vaginitis", "Bacterial vaginosis", "VAGINOSIS BACTERIAL", "vaginitis bacterial", "Bacterial Vaginoses", "Bacterial Vaginosis", "bacterial vaginosis", "Bacterial Vaginitis", "Bacterial vaginitis", "bacterial vaginoses", "Vaginosis bacterial", "Vaginitis bacterial", "BACTERIAL VAGINOSIS", "Vaginosis, Bacterial", "Vaginitis, Bacterial", "Vaginoses, Bacterial", "gardnerella vaginosis", "gardnerella vaginitis", "nonspecific vaginitis", "Bacterial Vaginitides", "NONSPECIFIC VAGINITIS", "Nonspecific Vaginitis", "gardnerella infection", "Nonspecific vaginitis", "Non-specific vaginitis", "Vaginitis, Nonspecific", "VAGINITIS NON SPECIFIC", "non specific vaginitis", "non-specific vaginitis", "Vaginitides, Bacterial", "VAGINOSIS NON SPECIFIC", "Vaginitis bacterial NOS", "Vaginosis bacterial NOS", "BV - Bacterial vaginosis", "AV - Anaerobic vaginosis", "NSV - Nonspecific vaginitis", "Bacterial vaginosis (disorder)", "Nonspecific bacterial vaginosis", "gardnerella vaginalis vaginitis", "bacterial vaginitis (diagnosis)", "bactria infection of the vagina", "nonspecific vaginitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bacterial vaginosis", "shortest_name_length": 2}
{"curie": "MONDO:0001303", "names": ["Pupil Disorders", "PUPIL FUNCTION ANOMALY", "abnormal pupil function", "pupillary function anomaly", "Anomaly;pupillary function", "Pupil function abnormality", "Pupillary function anomaly", "Abnormal pupillary function", "Abnormal Pupillary Function", "abnormal pupillary function", "Abnormal Pupillary Functions", "Pupillary Function, Abnormal", "Pupillary Functions, Abnormal", "anomalies of pupillary function", "Anomalies of pupillary function", "Abnormal pupillary function, NOS", "pupil; anomaly, function (reaction)", "anomaly; pupil, function (reaction)", "Other anomalies of pupillary function", "abnormal pupillary function (disease)", "Abnormal pupillary function (disorder)", "Abnormal pupillary function, unspecified", "anomalies of pupillary function (diagnosis)", "abnormal pupillary function (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "abnormal pupillary function", "shortest_name_length": 15}
{"curie": "UMLS:C0151511", "names": ["Mastatrophy", "MASTATROPHY", "Atrophy breast", "BREAST ATROPHY", "Breast atrophy", "breast atrophy", "Breast Atrophy", "ATROPHY BREAST", "breast; atrophy", "atrophy; breast", "Atrophy of breast", "atrophy of breast", "Breast size decrease", "BREAST SIZE DECREASE", "breast atrophy (diagnosis)", "Atrophy of breast (disorder)", "atrophy of breast (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atrophy of breast", "shortest_name_length": 11}
{"curie": "MONDO:0004677", "names": ["Tinea nigra", "tinea nigra", "tinea; nigra", "nigra; tinea", "Pityriasis nigra", "pityriasis; nigra", "nigra; pityriasis", "microsporosis nigra", "Microsporosis nigra", "Tinea palmaris nigra", "nigra; microsporosis", "microsporosis; nigra", "Tinea nigra (disorder)", "keratomycosis nigricans", "Cladosporium; werneckii", "tinea nigra (diagnosis)", "Keratomycosis nigricans", "Hortaea werneckii infection", "Microsporosis nigra (disorder)", "Keratomycosis nigricans palmaris", "Infection by Cladosporium werneckii", "infection by Cladosporium werneckii", "Infection caused by Cladosporium werneckii", "Infection caused by Cladosporium werneckii (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tinea nigra", "shortest_name_length": 11}
{"curie": "MONDO:0040700", "names": ["Orbit Dermoid Cyst", "orbit dermoid cyst", "orbital dermoid cyst", "Dermoid Cyst of Orbit", "dermoid cyst of orbit", "Dermoid cyst of orbit", "epidermal dermoid cyst", "dermoid cyst of the orbit", "Dermoid Cyst of the Orbit"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orbital dermoid cyst", "shortest_name_length": 18}
{"curie": "UMLS:C5418968", "names": ["Mediastinal Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mediastinal Non-Hodgkin Lymphoma", "shortest_name_length": 32}
{"curie": "UMLS:C0751759", "names": ["Non-24-hour sleep-wake disorder", "Non 24 Hour Sleep Wake Disorder", "Non-24 Hour Sleep-Wake Disorder", "Sleep-Wake Disorder, Non-24 Hour", "Sleep Wake Disorder, Non 24 Hour"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-24 Hour Sleep-Wake Disorder", "shortest_name_length": 31}
{"curie": "MONDO:0018791", "names": ["Moyomoya angiopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Moyomoya angiopathy", "shortest_name_length": 19}
{"curie": "UMLS:C4725860", "names": ["Refractory Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Liposarcoma", "shortest_name_length": 22}
{"curie": "MONDO:0000169", "names": ["microphthalmia, isolated, with cataract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microphthalmia, isolated, with cataract", "shortest_name_length": 39}
{"curie": "MONDO:0003749", "names": ["ESOPHAGEAL", "ulcer esophagus", "Esophagus ulcer", "esophagus ulcer", "esophagus; ulcer", "Esophageal ulcer", "Ulcer esophageal", "ESOPHAGEAL ULCER", "esophageal ulcer", "ulcer; esophagus", "ULCER ESOPHAGEAL", "esophagus ulcers", "Esophageal Ulcer", "Oesophagus ulcer", "ulcer oesophagus", "esophageal Ulcer", "Oesophageal ulcer", "Esophagus disease", "disease esophagus", "oesophageal ulcer", "esophagus disease", "Ulcer oesophageal", "esophageal ulcers", "Esophageal ulcers", "esophageal disease", "esophagus disorder", "diseases esophagus", "esophagus diseases", "Esophageal Disease", "Oesophagus disease", "ulcer of esophagus", "Ulcer of esophagus", "esophagus; disease", "disease oesophagus", "Esophageal disease", "Esophagus Disorders", "Esophageal Disorder", "Disease;oesophageal", "Disease, Esophageal", "esophageal diseases", "disorders esophagus", "Ulcer of oesophagus", "esophageal disorder", "oesophageal disease", "Esophageal disorder", "Esophageal Diseases", "Esophagus--Diseases", "ESOPHAGEAL DISORDER", "esophagus ulceration", "Esophagus ulceration", "Disease of esophagus", "Oesophageal disorder", "ESOPHAGUS ULCERATION", "Diseases, Esophageal", "disease of esophagus", "esophageal disorders", "Esophageal disorders", "Diseases of esophagus", "Disease of oesophagus", "Oesophagus ulceration", "Esophageal ulceration", "ESOPHAGEAL ULCERATION", "DISEASES OF ESOPHAGUS", "Disorder of esophagus", "esophageal ulceration", "disorders oesophageal", "OU - Esophageal ulcer", "diseases of esophagus", "disorder of esophagus", "disease of oesophagus", "oesophageal ulceration", "esophageal dysfunction", "OESOPHAGEAL ULCERATION", "Ulceration;oesophageal", "Ulcer of esophagus NOS", "esophageal ulcerations", "Esophageal disease NOS", "Disorder of oesophagus", "Oesophageal ulceration", "DISEASES OF OESOPHAGUS", "OU - Oesophageal ulcer", "ESOPHAGEAL DYSFUNCTION", "diseases of oesophagus", "Ulcer of esophagus, NOS", "Esophageal disorder NOS", "Oesophageal disease NOS", "Oesophageal disorder NOS", "Ulcer of oesophagus, NOS", "diseases of the esophagus", "DISEASES OF THE ESOPHAGUS", "Disease of esophagus, NOS", "Peptic ulcer of esophagus", "Peptic ulcer of oesophagus", "Disorder of esophagus, NOS", "Disease of oesophagus, NOS", "Disorder of oesophagus, NOS", "Esophageal ulcer (diagnosis)", "diseases disorders esophagus", "esophageal ulcer (diagnosis)", "Ulcer of esophagus (disorder)", "esophagus disease or disorder", "Peptic ulceration of esophagus", "Peptic ulceration of oesophagus", "esophageal disorders (diagnosis)", "disease or disorder of esophagus", "Disorder of esophagus (disorder)", "Unspecified disorder of esophagus", "Disease of esophagus, unspecified", "Unspecified disorder of oesophagus", "Disease of oesophagus, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophageal disorder", "shortest_name_length": 10}
{"curie": "UMLS:C0027643", "names": ["Local Neoplasm Recurrence", "Recurrence, Local Neoplasm", "Neoplasm Recurrence, Local", "Local Neoplasm Recurrences", "Recurrences, Local Neoplasm", "Neoplasm Recurrences, Local", "Locoregional Neoplasm Recurrence", "Locoregional Neoplasm Recurrences", "Recurrence, Locoregional Neoplasm", "Neoplasm Recurrence, Locoregional", "Recurrences, Locoregional Neoplasm", "Neoplasm Recurrences, Locoregional"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplasm Recurrence, Local", "shortest_name_length": 25}
{"curie": "MONDO:0010331", "names": ["Chds3", "CHDS3", "CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 3", "coronary heart disease, susceptibility to, 3", "coronary heart disease, susceptibility to, type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coronary heart disease, susceptibility to, 3", "shortest_name_length": 5}
{"curie": "MONDO:0016311", "names": ["Bockenheimer syndrome", "genuine diffuse phlebectasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bockenheimer syndrome", "shortest_name_length": 21}
{"curie": "MONDO:0030440", "names": ["CORD22", "cone-rod dystrophy 22", "CONE-ROD DYSTROPHY 22"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cone-rod dystrophy 22", "shortest_name_length": 6}
{"curie": "UMLS:C0400877", "names": ["ileus postoperative", "Postoperative ileus", "Postoperative ileus (disorder)", "Postoperative ileus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postoperative ileus", "shortest_name_length": 19}
{"curie": "MONDO:0011790", "names": ["THMD3", "MCPHA", "Amish Microcephaly", "Amish microcephaly", "microcephaly, Amish type", "MICROCEPHALY, AMISH TYPE", "Microcephaly, Amish type", "AMISH LETHAL MICROCEPHALY", "Amish lethal microcephaly", "Amish lethal microcephaly (disorder)", "thiamine metabolism dysfunction syndrome 3 (microcephaly type)", "THIAMINE METABOLISM DYSFUNCTION SYNDROME 3 (MICROCEPHALY TYPE)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Amish lethal microcephaly", "shortest_name_length": 5}
{"curie": "MONDO:0020379", "names": ["early-onset zonular cataract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early-onset zonular cataract", "shortest_name_length": 28}
{"curie": "MONDO:0017417", "names": ["Ivemark's syndrome", "Ivemark II syndrome", "Renohepaticopancreatic dysplasia", "Renal hepatic pancreatic dysplasia", "Renal-hepatic-pancreatic dysplasia", "RENAL-HEPATIC-PANCREATIC DYSPLASIA", "renal-hepatic-pancreatic dysplasia", "Renal-Hepatic-Pancreatic Dysplasia", "Renal hepatic pancreatic dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal-hepatic-pancreatic dysplasia", "shortest_name_length": 18}
{"curie": "MONDO:0032829", "names": ["NEDHIB", "NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND VARIABLE INTELLECTUAL AND BEHAVIORAL ABNORMALITIES", "neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities", "shortest_name_length": 6}
{"curie": "MONDO:0010912", "names": ["CFEOM3A", "FEOM3 LOCUS", "Feom3 locus", "fibrosis of extraocular muscles, congenital, 3A", "TUBB3 congenital fibrosis of extraocular muscles", "congenital fibrosis of the extraocular muscles 3A", "congenital fibrosis of extraocular muscles caused by mutation in TUBB3", "FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3A, WITH OR WITHOUT EXTRAOCULAR INVOLVEMENT", "fibrosis of extraocular muscles, congenital, 3A, with or without extraocular involvement", "Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibrosis of extraocular muscles, congenital, 3A, with or without extraocular involvement", "shortest_name_length": 7}
{"curie": "MONDO:0011792", "names": ["TDH6", "thyroid dyshormonogenesis 6", "Thyroid Dyshormonogenesis 6", "THYROID DYSHORMONOGENESIS 6", "thyroid dyshormonogenesis type 6", "DUOX2 familial thyroid dyshormonogenesis", "genetic defect in thyroid hormonogenesis 6", "thyroid hormonogenesis, genetic defect in, 6", "THYROID HORMONOGENESIS, GENETIC DEFECT IN, 6", "Thyroid Hormonogenesis, Genetic Defect in, 6", "HYPOTHYROIDISM, CONGENITAL, DUE TO DYSHORMONOGENESIS, 6", "hypothyroidism, congenital, due to dyshormonogenesis, 6", "Hypothyroidism, Congenital, due to Dyshormonogenesis, 6", "familial thyroid dyshormonogenesis caused by mutation in DUOX2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid dyshormonogenesis 6", "shortest_name_length": 4}
{"curie": "MONDO:0007558", "names": ["BOE", "Benign Occipital Epilepsy", "benign occipital epilepsy", "Benign occipital epilepsy", "Occipital Epilepsy, Benign", "epilepsy, benign occipital", "EPILEPSY, BENIGN OCCIPITAL", "Epilepsy, Benign Occipital", "Benign Occipital Epilepsies", "Epilepsies, Benign Occipital", "Occipital Epilepsies, Benign", "occipital lobe epilepsy benign", "Benign occipital lobe epilepsy", "Benign occipital lobe epilepsy (disorder)", "Benign occipital lobe epilepsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign occipital epilepsy", "shortest_name_length": 3}
{"curie": "UMLS:C4288050", "names": ["Uterine Corpus Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Corpus Germ Cell Tumor", "shortest_name_length": 30}
{"curie": "MONDO:0011314", "names": ["GRD2", "Grd2", "Graves disease, susceptibility to, 2", "GRAVES DISEASE, SUSCEPTIBILITY TO, 2", "Graves disease, susceptibility to, type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Graves disease, susceptibility to, 2", "shortest_name_length": 4}
{"curie": "MONDO:0006576", "names": ["Ludwig", "Ludwig angina", "Ludwig Angina", "ludwig angina", "angina ludwig", "ludwigs angina", "angina; Ludwig", "anginas ludwig", "ANGINA, LUDWIG", "Ludwig; angina", "Ludwigs Angina", "Ludwig's Angina", "ludwig's angina", "Ludwig's angina", "Angina, Ludwig's", "Ludwig's angina syndrome", "Ludwig's angina (disorder)", "Ludwig's angina (diagnosis)", "Cellulitis of mouth (floor)", "Cellulitis of floor of mouth", "cellulitis of floor of mouth", "Submandibular space infection", "Submandibular Space Infection", "Submandibular Space Infections", "mouth floor cellulitis (disease)", "cellulitis (disease) of mouth floor", "Cellulitis of floor of mouth (disorder)", "cellulitis of floor of mouth (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ludwig's angina", "shortest_name_length": 6}
{"curie": "UMLS:C1266058", "names": ["Endometrioid adenocarcinoma, ciliated cell variant", "Ciliated Uterine Corpus Endometrioid Adenocarcinoma", "Endometrial Endometrioid Adenocarcinoma, Ciliated Variant", "Endometrioid adenocarcinoma, ciliated cell variant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endometrioid adenocarcinoma, ciliated cell variant", "shortest_name_length": 50}
{"curie": "MONDO:0014152", "names": ["LVNC8", "CMD1LL", "dilated cardiomyopathy 1LL", "cardiomyopathy, dilated, 1Ll", "CARDIOMYOPATHY, DILATED, 1LL", "LEFT VENTRICULAR NONCOMPACTION 8", "left ventricular noncompaction 8", "left ventricular noncompaction type 8", "PRDM16 familial isolated dilated cardiomyopathy", "familial isolated dilated cardiomyopathy caused by mutation in PRDM16"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "left ventricular noncompaction 8", "shortest_name_length": 5}
{"curie": "MONDO:0004530", "names": ["cervical microinvasive adenocarcinoma", "Cervical Microinvasive Adenocarcinoma", "early invasive cervical adenocarcinoma", "Early Invasive Cervical Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early invasive cervical adenocarcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0019440", "names": ["DRA", "amyloidosis beta2m", "AH type amyloidosis", "ABeta2Mwt amyloidosis", "amyloidosis dialysis-related", "dialysis-related amyloidosis", "dialysis-related arthropathy", "Dialysis-related amyloidosis", "Dialysis-related arthropathy", "wild type ABeta2M amyloidosis", "Wild type ABeta2M amyloidosis", "Dialysis-associated amyloidosis", "Beta-2-microglobulin amyloidosis", "Beta-2 microglobulin amyloidosis", "beta-2-Microglobulin amyloidosis", "Hemodialysis-associated amyloidosis", "hemodialysis-associated; amyloidosis", "amyloidosis; hemodialysis-associated", "Haemodialysis-associated amyloidosis", "wild type ABeta2-microglobulinic amyloidosis", "Wild type ABeta2-microglobulinic amyloidosis", "Hemodialysis-associated amyloidosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "wild type ABeta2M amyloidosis", "shortest_name_length": 3}
{"curie": "UMLS:C4745248", "names": ["Metastatic Kidney Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Kidney Carcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0007211", "names": ["HTNB", "BILGINTURAN SYNDROME", "Bilginturan syndrome", "Bilginturan brachydactyly", "brachydactyly with hypertension", "Brachydactyly with hypertension", "BRACHYDACTYLY WITH HYPERTENSION", "Hypertension With Brachydactyly", "hypertension and brachydactyly syndrome", "HYPERTENSION AND BRACHYDACTYLY SYNDROME", "Brachydactyly-arterial hypertension syndrome", "brachydactyly-arterial hypertension syndrome", "Brachydactyly and arterial hypertension syndrome", "type E brachydactyly with short stature and hypertension", "brachydactyly type E with short stature and hypertension", "Brachydactyly type E with short stature and hypertension", "brachydactyly type E, with short stature and hypertension", "Brachydactyly type E, with short stature and hypertension", "Brachydactyly, Type E, With Short Stature And Hypertension", "BRACHYDACTYLY, TYPE E, WITH SHORT STATURE AND HYPERTENSION", "brachydactyly, type E, with short stature and hypertension", "Brachydactyly and arterial hypertension syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly-arterial hypertension syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C5667218", "names": ["Transformed Indolent B-Cell Non-Hodgkin Lymphoma to Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transformed Indolent B-Cell Non-Hodgkin Lymphoma to Diffuse Large B-Cell Lymphoma", "shortest_name_length": 81}
{"curie": "UMLS:C1266035", "names": ["Mucinous Bronchioloalveolar Carcinoma", "Mucinous Bronchoalveolar Lung Carcinoma", "Mucinous Bronchioloalveolar Lung Carcinoma", "Mucinous Minimally Invasive Lung Adenocarcinoma", "Minimally Invasive Lung Mucinous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Minimally Invasive Lung Mucinous Adenocarcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0002522", "names": ["TGCT", "TSGCT", "Diffuse-type GCT", "tenosynovial giant cell tumor", "Diffuse-type giant cell tumor", "Tenosynovial Giant Cell Tumor", "Tenosynovial giant cell tumor", "Tenosynovial giant cell tumour", "tenosynovial giant cell tumour", "Tendon Sheath Giant Cell Tumor", "tendon sheath giant cell tumor", "Tendon sheath giant cell tumor", "TENDON SHEATH, GIANT CELL TUMOR", "giant cell tumor of Tenosynovium", "Giant Cell Tumor of Tenosynovium", "Pigmented villonodular synovitis", "tenosynovial giant cell neoplasm", "Tenosynovial Giant Cell Neoplasm", "Giant cell tumor of Tenosynovium", "tendon sheath giant cell neoplasm", "Giant cell tumour of Tenosynovium", "Giant Cell Tumor of Tendon Sheath", "Giant cell tumor of tendon sheath", "Tendon Sheath Giant Cell Neoplasm", "giant cell tumor of tendon sheath", "Giant cell tumour of tendon sheath", "Giant Cell Neoplasm of Tenosynovium", "giant cell neoplasm of Tenosynovium", "giant cell neoplasm of tendon sheath", "Giant Cell Tumor of the Tenosynovium", "Giant Cell Neoplasm of Tendon Sheath", "giant cell tumor of the Tenosynovium", "fibrous histiocytoma of tendon sheath", "Fibrous histiocytoma of tendon sheath", "Fibrous Histiocytoma of Tendon Sheath", "Giant Cell Neoplasm of the Tenosynovium", "giant cell neoplasm of the Tenosynovium", "giant cell tumor of tendon sheath (diagnosis)", "Fibrous histiocytoma of tendon sheath (disorder)", "Tenosynovial giant cell tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tenosynovial giant cell tumor", "shortest_name_length": 4}
{"curie": "UMLS:C4683668", "names": ["Centroblastic Lymphoma by Ann Arbor Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Centroblastic Lymphoma by Ann Arbor Stage", "shortest_name_length": 41}
{"curie": "UMLS:C1336969", "names": ["Virus-Related Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Virus-Related Sarcoma", "shortest_name_length": 21}
{"curie": "MONDO:0016701", "names": ["oligoastrocytic tumor", "mixed oligodendroglial and astrocytic tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oligoastrocytic tumor", "shortest_name_length": 21}
{"curie": "UMLS:C5419802", "names": ["Colon Neuroendocrine Tumor G3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colon Neuroendocrine Tumor G3", "shortest_name_length": 29}
{"curie": "MONDO:0043240", "names": ["Hemophilic arthritis", "hemophilic arthritis", "Hemophilic Arthritis", "HEMOPHILIC ARTHRITIS", "Haemophilic arthritis", "Hemophilic arthropathy", "hemophilic arthropathy", "arthropathy hemophilic", "hemophilia arthropathy", "ARTHROPATHY HEMOPHILIC", "Arthropathy, hemophilic", "haemophilia arthropathy", "Haemophilic arthropathy", "arthropathy in hemophilia", "Arthropathy in hemophilia", "Arthropathy in haemophilia", "Arthrohemorrhagic syndrome", "Hemophilic arthropathy (disorder)", "arthropathy hemophilic (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemophilic arthropathy", "shortest_name_length": 20}
{"curie": "UMLS:C5419664", "names": ["Advanced Primary Cutaneous T-Cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Primary Cutaneous T-Cell Non-Hodgkin Lymphoma", "shortest_name_length": 54}
{"curie": "MONDO:0014211", "names": ["CILD26", "primary ciliary dyskinesia 26", "CILIARY DYSKINESIA, PRIMARY, 26", "ciliary dyskinesia, primary, 26", "CFAP298 primary ciliary dyskinesia", "primary ciliary dyskinesia type 26", "ciliary dyskinesia, primary, type 26", "primary ciliary dyskinesia caused by mutation in CFAP298", "primary ciliary dyskinesia 26 with or without situs inversus", "CILIARY DYSKINESIA, PRIMARY, 26, WITH OR WITHOUT SITUS INVERSUS", "ciliary dyskinesia, primary, 26, with or without situs inversus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia 26", "shortest_name_length": 6}
{"curie": "MONDO:0008064", "names": ["Absent nasal cartilage", "Missing nasal cartilage", "Nasal Bones, Absence of", "nasal bones, absence of", "Absent cartilage of nose", "Missing cartilage of nose", "Agenesis of nasal cartilage", "Agenesis of nasal cartilages", "Agenesis of cartilage of nose", "Nasal Cartilages, Agenesis of", "Agenesis of nasal cartilages (disorder)", "Failure of development of nasal cartilage", "Failure of development of cartilage of nose"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasal bones, absence of", "shortest_name_length": 22}
{"curie": "MONDO:0021674", "names": ["Post-viral disorder", "post-viral disorder", "sequela of viral disease", "Disorder following viral disease", "Disorder following viral disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "post-viral disorder", "shortest_name_length": 19}
{"curie": "MONDO:0016001", "names": ["2-Hga", "2-HGA", "2-Hydroxyglutaricaciduria", "2-hydroxyglutaric aciduria", "2-Hydroxyglutaric Aciduria", "2-Hydroxyglutaric aciduria", "2-hydroxyglutaric acidemia", "2-hydroxyglutaric aciduria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "2-hydroxyglutaric aciduria", "shortest_name_length": 5}
{"curie": "MONDO:0015674", "names": ["LINCL", "late infantile NCL", "Late infantile NCL", "Bielschowsky-Jansky disease", "Jansky-Bielschowsky disease", "Bielschowsky-jansky disease", "JANSKY-BIELSCHOWSKY DISEASE", "Jansky Bielschowsky Disease", "Jansky-Bielschowsky Disease", "jansky-bielschowsky disease", "bielschowsky disease jansky", "Disease, Jansky-Bielschowsky", "Dollinger-Bielschowsky syndrome", "dollinger-Bielschowsky syndrome", "Neuronal lipofuscinosis, infantile", "neuronal ceroid lipofuscinosis CLN2", "jansky-Bielschowsky amaurotic idiocy", "amaurotic idiocy early juvenile type", "Amaurotic idiocy late infantile type", "Amaurotic idiocy early juvenile type", "amaurotic idiocy late infantile type", "amaurotic idiocy, late infantile type", "Amaurotic idiocy, early juvenile type", "Amaurotic idiocy, late infantile type", "Neuronal Ceroid Lipofuscinosis Type 2", "amaurotic idiocy, early juvenile type", "Late-Infantile Neuronal Ceroid Lipfuscinosis", "late-infantile neuronal ceroid lipofuscinosis", "Late-Infantile Neuronal Ceroid Lipofuscinosis", "late infantile neuronal ceroid lipofuscinosis", "Late infantile neuronal ceroid lipofuscinosis", "Late Infantile Neuronal Ceroid Lipofuscinosis", "Late-infantile neuronal ceroid lipofuscinosis", "Neuronal Ceroid Lipofuscinosis, Late-Infantile", "Neuronal Ceroid Lipofuscinosis, Late Infantile", "NEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE", "neuronal ceroid lipofuscinosis CLN2 (diagnosis)", "Bielschowsky-jansky type neuronal ceroid lipofuscinosis", "Bielschowsky-Jansky type neuronal ceroid lipofuscinosis", "Late-infantile neuronal ceroid lipofuscinosis (disorder)", "Dollinger-Bielschowsky type neuronal ceroid lipofuscinosis", "dollinger-Bielschowsky type neuronal ceroid lipofuscinosis", "neuronal ceroid lipofuscinosis CLN2 (Jansky-Bielschowsky disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "late infantile neuronal ceroid lipofuscinosis", "shortest_name_length": 5}
{"curie": "UMLS:C1334158", "names": ["Immunodeficiency-Related Burkitt Lymphoma", "Immunodeficiency Related Burkitt Lymphoma", "Immunodeficiency Related Burkitt's Lymphoma", "Immunodeficiency-Related Burkitt's Lymphoma", "Immunodeficiency Associated Burkitt Lymphoma", "Immunodeficiency-associated Burkitt lymphoma", "Immunodeficiency-Associated Burkitt Lymphoma", "Immunodeficiency Associated Burkitt's Lymphoma", "Immunodeficiency-Associated Burkitt's Lymphoma", "Immunodeficiency-associated Burkitt's lymphoma", "Immunodeficiency-associated Burkitt's lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immunodeficiency-associated Burkitt's lymphoma", "shortest_name_length": 41}
{"curie": "MONDO:0010223", "names": ["Ichthyosis, X-Linked, without Steroid Sulfatase Deficiency", "ichthyosis, X-linked, without steroid sulfatase deficiency", "ICHTHYOSIS, X-LINKED, WITHOUT STEROID SULFATASE DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ichthyosis, X-linked, without steroid sulfatase deficiency", "shortest_name_length": 58}
{"curie": "UMLS:C0860191", "names": ["Injection site hypesthesia", "Injection site hypoesthesia", "Injection site hypaesthesia", "Injection site hypoaesthesia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site hypoesthesia", "shortest_name_length": 26}
{"curie": "UMLS:C3273137", "names": ["Extrahepatic Bile Duct Lymphoma", "Primary Extrahepatic Bile Duct Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extrahepatic Bile Duct Lymphoma", "shortest_name_length": 31}
{"curie": "MONDO:0005533", "names": ["colitis distal", "Distal colitis", "distal colitis", "left colon inflammation", "Distal colitis (disorder)", "inflammation of left colon", "distal colitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal colitis", "shortest_name_length": 14}
{"curie": "UMLS:C0278836", "names": ["stage III prostate cancer", "Prostate cancer stage III", "Stage III Prostate Cancer", "cancer iii prostate stage", "stage iii prostate cancer", "prostate cancer, stage III", "Prostatic cancer stage III", "Stage III Prostate Carcinoma", "stage III cancer of the prostate", "Stage III Prostate Cancer AJCC v6", "cancer of the prostate, stage III", "Prostate Cancer Stage III AJCC v6", "Stage III Prostatic Cancer AJCC v6", "stage III carcinoma of the prostate", "Carcinoma of the prostate stage III", "carcinoma of the prostate, Stage III", "Stage III Cancer of Prostate AJCC v6", "Prostate Carcinoma Stage III AJCC v6", "Stage III Prostate Carcinoma AJCC v6", "Cancer of Prostate Stage III AJCC v6", "Stage III Prostatic Carcinoma AJCC v6", "Stage III Cancer of the Prostate AJCC v6", "Cancer of the Prostate Stage III AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Prostate Carcinoma", "shortest_name_length": 25}
{"curie": "UMLS:C4725601", "names": ["Recurrent Chronic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Chronic Leukemia", "shortest_name_length": 26}
{"curie": "UMLS:C2931290", "names": ["Distal myopathy Swedish type", "Distal myopathy Welander type", "Distal myopathy, Swedish type", "Welander distal myopathy, Swedish type", "Distal myopathy Welander type (disorder)", "Distal myopathy Welander type (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Welander distal myopathy, Swedish type", "shortest_name_length": 28}
{"curie": "MONDO:0018509", "names": ["small intestinal squamous cell cancer", "Small Intestinal Squamous Cell Cancer", "small intestine squamous cell carcinoma", "small intestinal squamous cell carcinoma", "Small Intestinal Squamous Cell Carcinoma", "squamous cell carcinoma of the small bowel", "squamous cell carcinoma of the small intestine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "squamous cell carcinoma of the small intestine", "shortest_name_length": 37}
{"curie": "UMLS:C5420031", "names": ["Head and Neck NUT Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Head and Neck NUT Carcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0044312", "names": ["ISDNA", "immunoskeletal dysplasia with neurodevelopmental abnormalities", "IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES", "IMMUNOSKELETAL dysplasia with neurodevelopmental abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunoskeletal dysplasia with neurodevelopmental abnormalities", "shortest_name_length": 5}
{"curie": "MONDO:0001863", "names": ["aorta atresia", "Atresia and stenosis of aorta", "atresia and stenosis of aorta", "Congenital atresia and stenosis of aorta", "Atresia and stenosis of aorta (disorder)", "congenital atresia and stenosis of aorta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aorta atresia", "shortest_name_length": 13}
{"curie": "UMLS:C0752289", "names": ["Environmental Sleep Disorder", "Environmental sleep disorder", "Environmental Sleep Disorders", "Sleep Disorder, Environmental", "Sleep Disorders, Environmental", "Environmental sleep disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Environmental Sleep Disorder", "shortest_name_length": 28}
{"curie": "MONDO:0033007", "names": ["GAMOS3", "GALLOWAY-MOWAT SYNDROME 3", "Galloway-Mowat syndrome 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Galloway-Mowat syndrome 3", "shortest_name_length": 6}
{"curie": "MONDO:0011033", "names": ["T1D13", "IDDM13", "TYPE 1 DIABETES MELLITUS 13", "type 1 diabetes mellitus 13", "insulin-dependent diabetes mellitus 13", "Insulin-Dependent Diabetes Mellitus 13", "INSULIN-DEPENDENT DIABETES MELLITUS 13", "diabetes mellitus, insulin-dependent, 13", "DIABETES MELLITUS, INSULIN-DEPENDENT, 13", "Diabetes Mellitus, Insulin-Dependent, 13"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type 1 diabetes mellitus 13", "shortest_name_length": 5}
{"curie": "UMLS:C4521907", "names": ["Stage II Rectosigmoid Cancer", "Stage II Rectosigmoid Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Rectosigmoid Cancer AJCC v7", "shortest_name_length": 28}
{"curie": "MONDO:0004895", "names": ["Accommodative esotropia", "accommodative esotropia", "Accommodative esotropia (disorder)", "accommodative esotropia (diagnosis)", "Accommodative component in esotropia", "Esotropia with accommodative element", "Esotropia with accommodative compensation", "Esotropia with accommodative compensation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "accommodative esotropia", "shortest_name_length": 23}
{"curie": "UMLS:C4525860", "names": ["Stage I Rectal Neuroendocrine Tumor", "Stage I Rectal Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Rectal Neuroendocrine Tumor AJCC v8", "shortest_name_length": 35}
{"curie": "MONDO:0005230", "names": ["cellulitis", "CELLULITIS", "Cellulitis", "Skin infection", "cellulitis nos", "Cellulitis NOS", "Cellulitis, NOS", "cellulitis hand", "Skin infections", "hand; cellulitis", "cellulitis; hand", "Cellulitis of Hand", "cellulitis of hand", "Cellulitis of hand", "cellulitis (disease)", "Cellulitis (disorder)", "bacterial skin disease", "cellulitis (diagnosis)", "Bacterial Skin Disease", "Bacterial Skin Disorder", "bacterial skin diseases", "skin bacterial diseases", "Disease, Bacterial Skin", "Skin Disease, Bacterial", "skin diseases bacterial", "Bacterial Skin Diseases", "Cellulitis, unspecified", "bacterial skin infection", "Skin Diseases, Bacterial", "skin bacterial infection", "bacterial skin disorders", "bacterial infection skin", "Skin bacterial infection", "bacterial infections skin", "Bacterial infection of skin", "Subcutaneous tissue inflamed", "Cellulitis of hand (disorder)", "cellulitis of hand (diagnosis)", "inflammation; subcutaneous tissue", "subcutaneous; inflammation, tissue", "Bacterial dermatological disorders", "subcutaneous; tissue, inflammation", "Inflammation of subcutaneous tissue", "bacterial dermatological conditions", "bacterial skin disorders (diagnosis)", "Cellulitis (morphologic abnormality)", "cellulitis of hand (physical finding)", "Bacterial infection of skin (disorder)", "Bacterial infection of skin and subcutis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cellulitis", "shortest_name_length": 10}
{"curie": "UMLS:C0280357", "names": ["Stage III Mouth Adenoid Cystic Carcinoma", "Stage III Oral Cavity Adenoid Cystic Cancer", "Stage III Adenoid Cystic Carcinoma of Mouth", "Stage III Oral Cavity Adenoid Cystic Carcinoma", "Stage III Adenoid Cystic Carcinoma of the Mouth", "oral cavity adenoid cystic carcinoma, stage III", "Stage III Adenoid Cystic Carcinoma of Oral Cavity", "Stage III Adenoid Cystic Carcinoma of the Oral Cavity", "stage III adenoid cystic carcinoma of the oral cavity", "Adenoid cystic carcinoma of the oral cavity stage III", "Stage III Oral Cavity Adenoid Cystic Carcinoma AJCC v7", "adenoid cystic carcinoma of the oral cavity, stage III", "Stage III Oral Cavity Adenoid Cystic Carcinoma AJCC v6", "Stage III Oral Cavity Adenoid Cystic Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenoid cystic carcinoma of the oral cavity stage III", "shortest_name_length": 40}
{"curie": "UMLS:C4527149", "names": ["IAC", "Intermediate Atypical mCRPC", "Intermediate Atypical Carcinoma", "Intermediate Atypical Prostate Carcinoma", "Intermediate Atypical Metastatic Castration-Resistant Prostate Cancer", "Intermediate Atypical Metastatic Castration-Resistant Prostate Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intermediate Atypical Prostate Carcinoma", "shortest_name_length": 3}
{"curie": "MONDO:0020347", "names": ["AIDP", "acute inflammatory polyneuropathy", "acute idiopathic demyelinating polyneuropathy", "acute inflammatory demyelinating polyradiculopathy", "Acute Inflammatory Demyelinating Polyradiculopathy", "acute inflammatory demyelinating polyradiculoneuropathy", "Acute Inflammatory Demyelinating Polyradiculoneuropathy", "GBS, acute inflammatory demyelinating polyradiculoneuropathic form", "Guillain-Barré syndrome, acute inflammatory demyelinating polyradiculoneuropathic form", "Guillain-Barre syndrome, acute inflammatory demyelinating polyradiculoneuropathic form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute inflammatory demyelinating polyradiculoneuropathy", "shortest_name_length": 4}
{"curie": "MONDO:0019056", "names": ["neuromyopathy", "Neuromyopathy", "neuromyopathies", "myoneural disorder", "Myoneural disorder", "Neuromyopathy, NOS", "Myoneural disorders", "MYONEURAL DISORDERS", "Neuromuscular Disease", "Neuromuscular disease", "neuromuscular disease", "disease neuromuscular", "NEUROMUSCULAR DISEASE", "neuromuscular diseases", "Neuromuscular diseases", "diseases neuromuscular", "Neuromuscular Disorder", "neuromuscular disorder", "Neuromyopathy syndrome", "Neuromuscular disorder", "Neuromuscular Diseases", "Myoneural disorder, NOS", "Neuromuscular disorders", "disorders neuromuscular", "neuromuscular disorders", "Neuromuscular Disorders", "Neuromyopathy (disorder)", "nerve and muscle disorder", "NEUROMUSCULAR DISEASE, NOS", "Neuromuscular disease, NOS", "Neuromuscular disorder NOS", "myoneural disorder (diagnosis)", "Myoneural disorder, unspecified", "Myoneural disorders, unspecified", "disease (or disorder); myoneural", "Neuromuscular disease or syndrome", "neuromuscular diseases (diagnosis)", "disease (or disorder); neuromuscular system", "General Neuromuscular Diseases and Syndromes", "Combined disorder of muscle AND peripheral nerve", "Diseases and Syndromes of the Nervous and Muscular Systems", "Combined disorder of muscle AND peripheral nerve (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuromuscular disease", "shortest_name_length": 13}
{"curie": "MONDO:0005394", "names": ["Brain Infarct", "Infarct, Brain", "Brain Infarcts", "Infarcts, Brain", "Brain infarction", "brain infarction", "infarction brain", "Brain Infarction", "brain infarctions", "Infarction, Brain", "Brain Infarctions", "Infarctions, Brain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brain infarction", "shortest_name_length": 13}
{"curie": "UMLS:C4744968", "names": ["Non-Neoplastic Genitourinary System Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Genitourinary System Disorder", "shortest_name_length": 44}
{"curie": "UMLS:C5552725", "names": ["MRX34", "MRX21", "Mental Retardation, X-linked 21/34"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mental Retardation, X-linked 21/34", "shortest_name_length": 5}
{"curie": "MONDO:0020529", "names": ["adrenal Cushing syndrome", "ACTH-independent Cushing syndrome", "corticotropin-independent Cushing syndrome", "adrenocorticotropic hormone-independent Cushing syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ACTH-independent Cushing syndrome", "shortest_name_length": 24}
{"curie": "MONDO:0019991", "names": ["FGN", "GOMMID", "Amyloid-like glomerulopathy", "immunotactoid glomerulopathy", "Immunotactoid Glomerulopathy", "Immunotachtoid glomerulopathy", "Fibrillary glomerulonephritis", "Fibrillary Glomerulonephritis", "fibrillary glomerulonephritis", "glomerulonephritis fibrillary", "Immunotactoid glomerulonephritis", "Fibrillary glomerulonephritis (disorder)", "Fibrillary glomerulonephritis (diagnosis)", "Non-Amyloid Fibrillary Glomerulonephritis", "Glomerulonephritis with Organized Monoclonal Microtubular Immunoglobulin Deposits"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunotactoid glomerulopathy", "shortest_name_length": 3}
{"curie": "UMLS:C4526655", "names": ["stage IIIB malignant mesothelioma", "Stage IIIB Pleural Malignant Mesothelioma", "Stage IIIB Pleural Malignant Mesothelioma AJCC v8", "stage IIIB pleural malignant mesothelioma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Pleural Malignant Mesothelioma AJCC v8", "shortest_name_length": 33}
{"curie": "MONDO:0014542", "names": ["CMS15", "CMSWTA", "congenital myasthenic syndrome 15", "myasthenic syndrome, congenital, 15", "MYASTHENIC SYNDROME, CONGENITAL, 15", "ALG14 congenital myasthenic syndrome", "congenital myasthenic syndrome type 15", "myasthenic syndrome, congenital, type 15", "congenital myasthenic syndrome caused by mutation in ALG14", "MYASTHENIC SYNDROME, CONGENITAL, WITHOUT TUBULAR AGGREGATES", "myasthenic syndrome, congenital, without tubular aggregates", "congenital myasthenic syndrome 15 without tubular aggregates", "myasthenic syndrome, congenital, 15, without tubular aggregates"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myasthenic syndrome 15", "shortest_name_length": 5}
{"curie": "UMLS:C2211454", "names": ["Skin Pleomorphic Liposarcoma", "pleomorphic liposarcoma of skin", "pleomorphic liposarcoma of skin (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pleomorphic liposarcoma of skin", "shortest_name_length": 28}
{"curie": "UMLS:C1335102", "names": ["Occupational Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Occupational Neoplasm", "shortest_name_length": 21}
{"curie": "MONDO:0007904", "names": ["Median nodule of upper lip", "LIP, MEDIAN NODULE OF UPPER", "LIP, MEDIAN NODULE of upper", "Median nodule of the upper lip", "median nodule of the upper lip", "Median nodule of upper lip (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "median nodule of the upper lip", "shortest_name_length": 26}
{"curie": "MONDO:0012125", "names": ["HLD2", "PMLD1", "GJC2 leukodystrophy", "hypomyelinating leukodystrophy 2", "Leukodystrophy, Hypomyelinating, 2", "LEUKODYSTROPHY, HYPOMYELINATING, 2", "leukodystrophy, hypomyelinating, 2", "Pelizaeus-Merzbacher-like disease 1", "Pelizaeus-Merzbacher-like disease, 1", "Pelizaeus-Merzbacher-Like Disease, 1", "PELIZAEUS-MERZBACHER-LIKE DISEASE, 1", "hypomyelinating leukodystrophy type 2", "leukodystrophy, hypomyelinating, type 2", "leukodystrophy caused by mutation in GJC2", "Pelizaeus-Merzbacher-like disease due to GJC2 mutation", "Pelizaeus Merzbacher like disease due to GJC2 mutation", "Pelizaeus Merzbacher like disease due to GJC2 mutation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypomyelinating leukodystrophy 2", "shortest_name_length": 4}
{"curie": "UMLS:C5670389", "names": ["SUPERNUMERARY BRANCH", "Supernumerary Branch"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Supernumerary Branch", "shortest_name_length": 20}
{"curie": "MONDO:0005670", "names": ["Blackwater Fever", "Blackwater fever", "blackwater fever", "black water fever", "Fever, Blackwater", "Hemolytic Malaria", "Black Water Fever", "Black water fever", "Blackwater Fevers", "Hemolytic Malarias", "Fever, Black Water", "Black Water Fevers", "Fevers, Blackwater", "Malaria, Hemolytic", "Fevers, Black Water", "Malarias, Hemolytic", "Hemoglobinuric fever", "Haemoglobinuric fever", "hemoglobinuric, malaria", "Malarial Hemoglobinuria", "malarial hemoglobinuria", "Hemoglobinuric, malaria", "Malarial hemoglobinuria", "hemoglobinuria; malarial", "Malarial haemoglobinuria", "malaria; blackwater fever", "blackwater fever; malarial", "Black water fever (disorder)", "black water fever (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blackwater fever", "shortest_name_length": 16}
{"curie": "MONDO:0014408", "names": ["MPPH3", "megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3", "MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 3", "megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome type 3", "CCND2 megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome", "megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome caused by mutation in CCND2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3", "shortest_name_length": 5}
{"curie": "UMLS:C4524730", "names": ["Pathologic Stage II Gastroesophageal Junction Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage II Gastroesophageal Junction Adenocarcinoma AJCC v8", "shortest_name_length": 68}
{"curie": "MONDO:0700158", "names": ["canine pancreatic carcinoma", "Canine Pancreatic Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canine pancreatic carcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C0339507", "names": ["Branch retinal vein occlusion with macular edema", "Branch retinal vein occlusion with macular oedema", "Branch retinal vein occlusion with macular edema (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Branch retinal vein occlusion with macular edema", "shortest_name_length": 48}
{"curie": "MONDO:0006088", "names": ["Appendix adenoma", "appendix adenoma", "Appendix Adenoma", "vermiform appendix adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "appendix adenoma", "shortest_name_length": 16}
{"curie": "UMLS:C4050147", "names": ["BNCT", "Benign Notochordal Cell Tumor", "Intraosseous Benign Notochordal Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Notochordal Cell Tumor", "shortest_name_length": 4}
{"curie": "MONDO:0008154", "names": ["OSTEOMAS OF MANDIBLE", "osteomas of mandible", "Osteomas Of Mandible"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteomas of mandible", "shortest_name_length": 20}
{"curie": "MONDO:0021225", "names": ["Uvea Tumor", "uvea tumor", "Uveal mass", "Uveal Tumor", "uveal tumor", "Tumor of Uvea", "uvea neoplasm", "tumor of uvea", "Uvea Neoplasm", "uveal neoplasm", "Uveal Neoplasm", "Uveal Neoplasms", "Neoplasm, Uveal", "Neoplasm of Uvea", "Neoplasms, Uveal", "neoplasm of uvea", "Tumor of the Uvea", "tumor of the uvea", "Neoplasm of the Uvea", "Uveal Tract Neoplasm", "neoplasm of the uvea", "Neoplasm of uveal tract", "uvea neoplasm (disease)", "eye neoplasm uveal tract", "Neoplasm of uveal tract (disorder)", "Neoplasm of uveal tract (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uvea neoplasm", "shortest_name_length": 10}
{"curie": "UMLS:C1370932", "names": ["Upper Urinary Tract Carcinoma", "Renal pelvis and ureter cancer", "Renal Pelvis and Ureter Cancer", "Renal Pelvis and Ureter Carcinoma", "Carcinoma of the Upper Urinary Tract", "cancer of the renal pelvis and ureter", "carcinoma of the renal pelvis and ureter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal Pelvis and Ureter Carcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0023068", "names": ["engelhard yatziv syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "engelhard yatziv syndrome", "shortest_name_length": 25}
{"curie": "UMLS:C5419904", "names": ["Intestinal Soft Tissue Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal Soft Tissue Neoplasm", "shortest_name_length": 31}
{"curie": "UMLS:C1331537", "names": ["aorta; sclerosis", "aortic sclerosis", "Aortic sclerosis", "AORTIC SCLEROSIS", "sclerosis; aortic", "Aortic valve sclerosis", "aortic valve; sclerosis", "aorta; sclerosis, valve", "aortic sclerosis (diagnosis)", "Aortic valve sclerosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aortic sclerosis", "shortest_name_length": 16}
{"curie": "MONDO:0013902", "names": ["AOVD2", "bicuspid aortic valve", "aortic valve stenosis", "AORTIC VALVE DISEASE 2", "aortic valve disease 2", "SMAD6 aortic valve disease", "aortic valve disease type 2", "aortic valve disease caused by mutation in SMAD6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic valve disease 2", "shortest_name_length": 5}
{"curie": "UMLS:C1518735", "names": ["Ovarian Signet Ring Stromal Tumor", "Ovarian Signet-Ring Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Signet Ring Stromal Tumor", "shortest_name_length": 33}
{"curie": "UMLS:C1708309", "names": ["Hamartoma of Mature Cardiac Myocytes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hamartoma of Mature Cardiac Myocytes", "shortest_name_length": 36}
{"curie": "UMLS:C1332510", "names": ["Benign Renal Hemangiopericytoma", "Benign Kidney Hemangiopericytoma", "Benign Hemangiopericytoma of Kidney", "Benign Hemangiopericytoma of the Kidney"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Kidney Hemangiopericytoma", "shortest_name_length": 31}
{"curie": "UMLS:C0854848", "names": ["Intestinal T-cell lymphoma stage IV", "Intestinal T-Cell Lymphoma Stage IV", "Stage IV Intestinal T-Cell Lymphoma", "Stage IV Enteropathy-type T-Cell Lymphoma", "Stage IV Enteropathy-Associated T-Cell Lymphoma", "Ann Arbor Stage IV Enteropathy-Associated T-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal T-cell lymphoma stage IV", "shortest_name_length": 35}
{"curie": "UMLS:C5200936", "names": ["delayed healing", "Healing delayed", "healing delayed", "healing impaired", "Slow healing wound", "delayed wound healing", "Delayed wound healing", "Wound healing delayed", "healing impaired wound", "of delayed wound healing", "Delayed healing of wound", "Delayed healing of wound (finding)", "delayed wound healing (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Delayed healing of wound", "shortest_name_length": 15}
{"curie": "UMLS:C5419774", "names": ["Ileal Neuroendocrine Tumor G3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ileal Neuroendocrine Tumor G3", "shortest_name_length": 29}
{"curie": "UMLS:C1333087", "names": ["Colon Ganglioneuroma", "Colonic Ganglioneuroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colon Ganglioneuroma", "shortest_name_length": 20}
{"curie": "MONDO:0007724", "names": ["Wiedemann Oldigs Oppermann syndrome", "Wiedemann-Oldigs-Oppermann syndrome", "HIRSUTISM, SKELETAL DYSPLASIA, AND MENTAL RETARDATION", "hirsutism, skeletal dysplasia, and mental retardation", "hirsutism-skeletal dysplasia-mental retardation syndrome", "Hirsutism skeletal dysplasia mental retardation syndrome", "hirsutism skeletal dysplasia mental retardation syndrome", "hirsutism, skeletal dysplasia, and intellectual disability", "Hirsutism, Skeletal Dysplasia, Mental Retardation Syndrome", "hirsutism skeletal dysplasia intellectual disability syndrome", "hirsutism-skeletal dysplasia-intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hirsutism-skeletal dysplasia-intellectual disability syndrome", "shortest_name_length": 35}
{"curie": "MONDO:0007381", "names": ["ERED", "COL17A1", "dystrophia Smolandiensis", "Dystrophia Smolandiensis", "Dystrophia Helsinglandica", "dystrophia Helsinglandica", "recurrent hereditary corneal erosions", "Recurrent hereditary corneal erosions", "CORNEAL EROSIONS, RECURRING HEREDITARY", "Corneal Erosions, Recurring Hereditary", "Epithelial recurrent erosion dystrophy", "Epithelial Recurrent Erosion Dystrophy", "epithelial recurrent erosion dystrophy", "corneal erosions, recurring hereditary", "EPITHELIAL RECURRENT EROSION DYSTROPHY", "Epithelial recurrent erosion dystrophy of cornea", "Epithelial recurrent erosion dystrophy of cornea (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epithelial recurrent erosion dystrophy", "shortest_name_length": 4}
{"curie": "UMLS:C4525296", "names": ["Gallbladder Cancer by AJCC v8 Stage", "Gallbladder Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gallbladder Cancer by AJCC v8 Stage", "shortest_name_length": 35}
{"curie": "MONDO:0001024", "names": ["lung; plague", "plague; lung", "plague pneumonic", "Pneumonic plague", "PLAGUE PNEUMONIA", "pneumonic plague", "Pneumonic Plague", "PLAGUE, PNEUMONIC", "pulmonary; plague", "plague; pulmonary", "pneumonic; plague", "plague; pneumonica", "Pneumonic plague, NOS", "primary pneumonic plague", "Primary pneumonic plague", "Secondary pneumonic plague", "secondary pneumonic plague", "Yersinia pestis; pneumonia", "pneumonia; Yersinia pestis", "Pneumonic plague (disorder)", "pneumonic plague (diagnosis)", "Pneumonic, unspecified plague", "Pneumonic plague, unspecified", "Primary pneumonic plague (disorder)", "primary pneumonic plague (diagnosis)", "Secondary pneumonic plague (disorder)", "secondary pneumonic plague (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pneumonic plague", "shortest_name_length": 12}
{"curie": "MONDO:0004328", "names": ["Maxillary Sinus Adenocarcinoma", "maxillary sinus adenocarcinoma", "Adenocarcinoma of Maxillary Sinus", "adenocarcinoma of maxillary sinus", "Adenocarcinoma of maxillary sinus", "adenocarcinoma of the maxillary sinus", "Adenocarcinoma of the Maxillary Sinus", "Primary adenocarcinoma of maxillary sinus", "Adenocarcinoma of maxillary sinus (disorder)", "Adenocarcinoma of maxillary sinus (diagnosis)", "Primary adenocarcinoma of maxillary sinus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maxillary sinus adenocarcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0008992", "names": ["JHS", "OFDS VIII", "Juberg Hayward syndrome", "JUBERG-HAYWARD SYNDROME", "Juberg-Hayward Syndrome", "Juberg-Hayward syndrome", "OROCRANIODIGITAL SYNDROME", "Orocraniodigital syndrome", "Juberg Hayward syndrome (disorder)", "Oral-Facial-Digital Syndrome, Type VIII", "CLEFT LIP/PALATE WITH ABNORMAL THUMBS AND MICROCEPHALY", "cleft LIP/palate with abnormal thumbs and microcephaly", "Cleft Lip-Palate With Abnormal Thumbs And Microcephaly", "cleft lip/palate-abnormal thumbs-microcephaly syndrome", "Cleft lip/palate-abnormal thumbs-microcephaly syndrome", "CLEFT LIP/PALATE WITH RADIAL HEAD AND DIGITAL ANOMALIES", "Oral-Facial-Digital Syndrome with Hypoplastic Epiglottis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Juberg-Hayward syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C0154552", "names": ["Genitourinary Malfunction Arising from Mental Factor", "Genitourinary malfunction arising from mental factors"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Genitourinary malfunction arising from mental factors", "shortest_name_length": 52}
{"curie": "MONDO:0002214", "names": ["Brain Germinoma", "brain germinoma", "Germinoma of Brain", "germinoma of brain", "Germinoma of the Brain", "intracranial germinoma", "germinoma of the brain", "brain germinoma (disease)", "germinoma of brain (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brain germinoma", "shortest_name_length": 15}
{"curie": "MONDO:0009697", "names": ["LBD", "Epm2", "EPM2", "MELF", "Melf", "EPM2B", "EPM2A", "Lafora", "PME type 2", "LAFORA DISEASE", "Lafora Disease", "lafora disease", "Lafora disease", "lafora's disease", "Lafora's disease", "lafora body disease", "LAFORA BODY DISEASE", "Lafora Body Disease", "Lafora body disease", "Lafora body disorder", "Lafora Body Disorder", "Lafora Myoclonic Epilepsy", "Lafora disease (disorder)", "Lafora's myoclonic epilepsy", "Myoclonic Epilepsy of Lafora", "MYOCLONIC EPILEPSY OF LAFORA", "myoclonic epilepsy of Lafora", "Lafora body disease (diagnosis)", "Epilepsy Progressive Myoclonic 2", "epilepsy progressive myoclonic 2", "Epilepsy, Progressive Myoclonic 2B", "EPILEPSY, PROGRESSIVE MYOCLONIC 2B", "Epilepsy, Progressive Myoclonic 2A", "EPILEPSY, PROGRESSIVE MYOCLONIC, 2A", "epilepsy, progressive myoclonic, 2A", "epilepsy, progressive myoclonic, 2B", "EPILEPSY, PROGRESSIVE MYOCLONIC, 2B", "Lafora progressive myoclonic epilepsy", "Progressive Myoclonic Epilepsy Type 2", "Progressive myoclonic epilepsy type 2", "progressive myoclonus epilepsy type 2", "progressive myoclonic epilepsy type 2", "Progressive myoclonus epilepsy type 2", "Lafora Progressive Myoclonic Epilepsy", "Lafora Progressive Myoclonus Epilepsy", "Progressive Myoclonic Epilepsy, Lafora", "Epilepsy, Progressive Myoclonic, Lafora", "Lafora Type Progressive Myoclonic Epilepsy", "Progressive Myoclonic Epilepsy, Lafora Type", "epilepsy, progressive myoclonic 2A (Lafora)", "Progressive Myoclonus Epilepsy, Lafora Type", "epilepsy, progressive myoclonic 2B (Lafora)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lafora disease", "shortest_name_length": 3}
{"curie": "UMLS:C4725595", "names": ["Thoracic Esophagus Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thoracic Esophagus Squamous Cell Carcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0011266", "names": ["DM2", "PROMM", "ricker disease", "Ricker disease", "ricker syndrome", "RICKER SYNDROME", "Ricker Syndrome", "Ricker syndrome", "Syndrome, Ricker", "Ricker's syndrome", "MYOTONIC DYSTROPHY 2", "Myotonic Dystrophy 2", "myotonic dystrophy 2", "dystrophia myotonica 2", "Dystrophia Myotonica 2", "DYSTROPHIA MYOTONICA 2", "Dystrophia myotonica 2", "CNBP myotonic dystrophy", "Dystrophia Myotonica 2s", "Myotonic dystrophy type 2", "myotonic dystrophy type 2", "Proximal Myotonic Myopathy", "proximal myotonic myopathy", "Proximal myotonic myopathy", "PROXIMAL MYOTONIC MYOPATHY", "Proximal myotonic dystrophy", "dystrophia myotonica type 2", "Myotonic Myopathy, Proximal", "MYOTONIC MYOPATHY, PROXIMAL", "proximal myotonic dystrophy", "myotonic myopathy, proximal", "Myopathy, Proximal Myotonic", "Proximal Myotonic Myopathies", "Myopathies, Proximal Myotonic", "Myotonic Myopathies, Proximal", "PROMM (Proximal Myotonic Myopathy)", "Proximal myotonic myopathy (PROMM)", "PROMMs (Proximal Myotonic Myopathy)", "Proximal myotonic myopathy (disorder)", "proximal myotonic dystrophy (diagnosis)", "myotonic dystrophy caused by mutation in CNBP"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myotonic dystrophy type 2", "shortest_name_length": 3}
{"curie": "MONDO:0032801", "names": ["EKVP6", "ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 6", "erythrokeratodermia variabilis et progressiva 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythrokeratodermia variabilis et progressiva 6", "shortest_name_length": 5}
{"curie": "MONDO:0700146", "names": ["canine prostate carcinoma", "Canine Prostate Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canine prostate carcinoma", "shortest_name_length": 25}
{"curie": "UMLS:C0854569", "names": ["Failure to anastomose", "Failure to Anastomose", "Failure To Anastomose", "Anastomose failure to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Failure to anastomose", "shortest_name_length": 21}
{"curie": "MONDO:0013452", "names": ["MSMDS", "multisystemic smooth muscle dysfunction syndrome", "Multisystemic smooth muscle dysfunction syndrome", "MULTISYSTEMIC SMOOTH MUSCLE DYSFUNCTION SYNDROME", "Multisystemic smooth muscle dysfunction syndrome (disorder)", "congenital mydriasis, patent ductus arteriosus, thoracic aortic aneurysm, and vasculopathy", "mydriasis, congenital, with patent ductus arteriosus, thoracic aortic aneurysm, and vasculopathy", "MYDRIASIS, CONGENITAL, WITH PATENT DUCTUS ARTERIOSUS, THORACIC AORTIC ANEURYSM, AND VASCULOPATHY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multisystemic smooth muscle dysfunction syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C1336091", "names": ["Larynx Verrucous Carcinoma in situ", "Stage 0 Larynx Verrucous Carcinoma", "Stage 0 Laryngeal Verrucous Carcinoma", "Laryngeal Verrucous Carcinoma in situ", "Verrucous Carcinoma in situ of Larynx", "Stage 0 Verrucous Carcinoma of Larynx", "Stage 0 Verrucous Carcinoma of the Larynx", "Verrucous Carcinoma in situ of the Larynx", "Stage 0 Laryngeal Throat Verrucous Cancer", "Stage 0 Laryngeal Verrucous Carcinoma AJCC v7", "Stage 0 Laryngeal Verrucous Carcinoma AJCC v8", "Stage 0 Laryngeal Verrucous Carcinoma AJCC v6", "Stage 0 Laryngeal Verrucous Carcinoma AJCC v6, v7, and v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Laryngeal Verrucous Carcinoma AJCC v6, v7, and v8", "shortest_name_length": 34}
{"curie": "MONDO:0004790", "names": ["Steatosis", "liver; fat", "fat; liver", "fatty liver", "FATTY LIVER", "LIVER FATTY", "Fatty liver", "Fatty Liver", "Liver fatty", "Liver, Fatty", "fatty livers", "steatohepatitis", "Steatohepatitis", "liver steatosis", "Liver Steatoses", "Liver Steatosis", "Liver steatosis", "Steatosis, Liver", "steatosis; liver", "Steatoses, Liver", "liver; steatosis", "STEATOSIS HEPATIC", "hepatic lipidosis", "Hepatic Steatosis", "Hepatic lipidosis", "Steatohepatitides", "Hepatic steatosis", "Steatosis hepatic", "hepatic steatosis", "Liver fatty change", "Steatosis of liver", "Steatosis of Liver", "liver fatty change", "fatty change liver", "LIVER FATTY CHANGE", "Visceral Steatoses", "change fatty liver", "steatosis of liver", "Visceral Steatosis", "Steatoses, Visceral", "fatty liver disease", "Steatosis, Visceral", "changes fatty liver", "hepatitic steatosis", "fatty change of liver", "alcoholic fatty liver", "Fatty change of liver", "Fatty changes in liver", "fatty liver (diagnosis)", "Infiltration fatty liver", "fatty infiltration liver", "Liver fatty degeneration", "liver fatty infiltration", "DEGENERATION FATTY LIVER", "FATTY LIVER INFILTRATION", "Degeneration fatty liver", "liver; infiltrate, fatty", "LIVER FATTY DEGENERATION", "LIVER FATTY INFILTRATION", "fatty liver infiltration", "infiltrate; liver, fatty", "INFILTRATION FATTY LIVER", "Liver fatty infiltration", "Fatty liver infiltration", "fatty; liver degeneration", "METAMORPHOSIS FATTY LIVER", "Liver fatty metamorphosis", "fatty; degeneration liver", "Fatty liver metamorphosis", "Metamorphosis fatty liver", "fatty liver metamorphosis", "LIVER FATTY METAMORPHOSIS", "Fatty metamorphosis, liver", "liver; degeneration, fatty", "Steatohepatitis (disorder)", "degeneration; fatty, liver", "degeneration; liver, fatty", "Fatty degeneration of liver", "steatohepatitis (diagnosis)", "Fatty infiltration of liver", "Steatosis of liver (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fatty liver disease", "shortest_name_length": 9}
{"curie": "UMLS:C4725110", "names": ["CNPC", "Castration-Naive Prostate Cancer", "Castration-Naive Prostate Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Castration-Naive Prostate Carcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0033367", "names": ["DEE58", "EIEE58", "infantile epileptic encephalopathy 58", "early infantile epileptic encephalopathy 58", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 58", "epileptic encephalopathy, early infantile, 58", "developmental and epileptic encephalopathy 58", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 58", "developmental and epileptic encephalopathy, 58"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 58", "shortest_name_length": 5}
{"curie": "MONDO:0009270", "names": ["Genitopalatocardiac syndrome", "GENITOPALATOCARDIAC SYNDROME", "GENITOPALATOCARDIAC syndrome", "Genito palato cardiac syndrome", "genito palato cardiac syndrome", "genito-palato-cardiac syndrome", "Genito-palato-cardiac syndrome", "GARDNER-SILENGO-WACHTEL SYNDROME", "Gardner-Silengo-Wachtel syndrome", "Gardner Silengo Wachtel syndrome", "Genitopalatocardiac syndrome (disorder)", "Male pseudohermaphroditism with micrognathia, cleft palate and conotruncal cardiac defect", "Male pseudohermaphroditism with micrognathia, cleft palate, and conotruncal Cardiac defect", "MALE PSEUDOHERMAPHRODITISM WITH MICROGNATHIA, CLEFT PALATE, AND CONOTRUNCAL CARDIAC DEFECT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genito-palato-cardiac syndrome", "shortest_name_length": 28}
{"curie": "UMLS:C4329971", "names": ["Factor XI Inactivation", "Factor XI Inhibitor Present"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Factor XI Inactivation", "shortest_name_length": 22}
{"curie": "UMLS:C0400839", "names": ["Rectal ulcer", "Ulcer rectal", "rectal ulcer", "Rectal Ulcer", "rectum ulcer", "ULCER RECTAL", "rectum; ulcer", "ulcer; rectum", "rectal ulcers", "Ulcer of rectum", "rectal ulceration", "RECTAL ULCERATION", "solitary rectal ulcer", "Solitary rectal ulcer", "rectal ulcer (diagnosis)", "Solitary ulcer of rectum", "Ulcer of rectum (disorder)", "rectal ulceration (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ulcer of rectum", "shortest_name_length": 12}
{"curie": "UMLS:C0036214", "names": ["EHS Tumor", "Tumor, EHS", "Engelbreth-Holm-Swarm Sarcoma", "Sarcoma, Engelbreth Holm Swarm", "Sarcoma, Engelbreth-Holm-Swarm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sarcoma, Engelbreth-Holm-Swarm", "shortest_name_length": 9}
{"curie": "MONDO:0007263", "names": ["Arrythmia", "ekg change", "Arrhythmia", "ecg change", "arrhythmia", "EKG CHANGE", "ARRHYTHMIA", "dysrhythmia", "Dysrhythmia", "Arrhythmias", "changes ecg", "changes ekg", "arrhythmias", "DYSRHYTHMIA", "Dysrhythmias", "Change in ECG", "HEART: RHYTHM", "Arrhythmia NOS", "Dysrhythmia(s)", "Arrhythmia, NOS", "Arrhythmia (NOS)", "rhythm; abnormal", "rhythm; disorder", "heart arrhythmia", "heart arrhythmias", "conduction defect", "Heart Arrhythmias", "Conduction defect", "Conduction Defects", "Cardiac Arrhythmia", "defect; conduction", "conduction; defect", "conductions defect", "Conduction defects", "abnormal heartbeat", "conduction defects", "CARDIAC ARRHYTHMIA", "Cardiac arrhythmia", "cardiac arrhythmia", "CONDUCTION DISORDER", "Arrhythmia, Cardiac", "Dysrhythmia;cardiac", "conduction disorder", "abnormal heart rate", "cardiac dysrhythmia", "Cardiac Dysrhythmia", "Abnormal heart beat", "Irregular heartbeat", "Abnormal heart rate", "Conduction disorder", "Cardiac dysrhythmia", "abnormal heart beat", "Heart rate abnormal", "Cardiac arrhythmias", "heart rate abnormal", "cardiac arrhythmias", "Cardiac Arrhythmias", "Arrhythmias (Heart)", "abnormal beats heart", "conduction disorders", "Irregular heart beat", "Arrhythmias, Cardiac", "cardiac; dysrhythmia", "dysrhythmia; cardiac", "CARDIAC DYSRHYTHMIAS", "Conduction disorders", "CONDUCTION DISORDERS", "Dysrhythmia, Cardiac", "Cardiac dysrhythmias", "cardiac dysrhythmias", "Cardiac rate disorder", "Abnormal cardiac rate", "Conduction Abnormality", "CARDIAC ARRHYTHMIA NOS", "Cardiac rate, abnormal", "Heart rhythm disorders", "Abnormal heart rhythms", "Cardiac arrhythmia NOS", "Cardiac arrhythmia nos", "cardiac rhythm disease", "Conduction disorder NOS", "heart beat; abnormality", "DEFECT CONDUCTION (NOS)", "abnormality; heart beat", "Ectopic beats all types", "disorder; rhythm, heart", "cardiac rhythm disorder", "rhythm, heart; abnormal", "Cardiac arrhythmia, NOS", "Cardiac arrhythmia (NOS)", "Arrhythmia cardiac (NOS)", "Cardiac rhythm irregular", "Arrhythmia (cardiac) NOS", "Cardiac dysrhythmia, NOS", "ARRHYTHMIA CARDIAC (NOS)", "CARDIAC ARRHYTHMIA (NOS)", "Electrocardiogram change", "Disorder of heart rhythm", "Cardiac rhythm, abnormal", "CARDIAC CONDUCTION DEFECT", "cardiac conduction system", "Electrocardiogram changes", "Heart conduction disorder", "Heart Conduction Disorder", "Cardiac conduction defects", "cardiac rhythm disturbance", "disturbance; rhythm, heart", "Abnormal cardiac rate, NOS", "Heartbeat (pulse);abnormal", "cardiac conduction defects", "Abnormalities of heart beat", "Cardiac conduction disorder", "Cardiac Conduction Disorder", "Change in electrocardiogram", "cardiac conduction disorder", "abnormalities of heart beat", "Cardiac rhythm disturbances", "Electrocardiographic Change", "Non specific EKG/ECG Changes", "Electrocardiographic changes", "Cardiac conduction disorders", "Electrocardiogram change NOS", "Disorder of heart conduction", "Changes in electrocardiogram", "Abnormal heart beat (finding)", "Cardiac arrhythmia (disorder)", "Disorder of Cardiac Conduction", "Cardiac conduction abnormality", "Abnormal cardiac rate (finding)", "conduction disorder (diagnosis)", "Cardiac arrhythmia, unspecified", "Conduction disorder of the heart", "Cardiac dysrhythmia, unspecified", "Cardiac conduction abnormalities", "Conduction disorder, unspecified", "CARDIAC CONDUCTION SYSTEM DISEASE", "Cardiac Conduction System Disease", "Abnormality of cardiac conduction", "Cardiac Conduction System Diseases", "cardiac rhythm disorder (diagnosis)", "CARDIAC ARRHYTHMIA, IRREGULAR PULSE", "[OBSOLETE] Cardiac Conduction Defect", "cardiac conduction system (diagnosis)", "Conduction disorder of the heart, NOS", "Unspecified abnormalities of heart beat", "Abnormality of cardiac conduction system", "Conduction disorder of the heart (disorder)", "abnormalities of heart beat (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiac rhythm disease", "shortest_name_length": 9}
{"curie": "MONDO:0020716", "names": ["TDH1", "thyroid dyshormonogenesis 1", "thyroid dyshormonogenesis type 1", "familial thyroid dyshormonogenesis 1", "genetic defect in thyroid hormonogenesis 1", "thyroid hormonogenesis, genetic defect in, 1", "iodine accumulation, transport, or trapping defect", "iodide accumulation, transport, or trapping defect", "hypothyroidism, congenital, due to dyshormonogenesis, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial thyroid dyshormonogenesis 1", "shortest_name_length": 4}
{"curie": "MONDO:0011768", "names": ["MYAS1", "Myas1", "Myasthenia Gravis with Thymus Hyperplasia", "MYASTHENIA GRAVIS WITH THYMUS HYPERPLASIA", "myasthenia gravis with thymus hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myasthenia gravis with thymus hyperplasia", "shortest_name_length": 5}
{"curie": "MONDO:0011366", "names": ["ovary germ cell tumor", "OVARY, GERM CELL TUMOR", "Ovarian Germ Cell Tumor", "Ovarian germ cell tumor", "ovarian germ cell tumor", "Germ Cell Tumor of Ovary", "Germ cell tumor of ovary", "germ cell ovarian cancer", "ovarian germ cell cancer", "cell germ ovaries tumors", "germ cell tumor, ovarian", "germ cell tumor of ovary", "Ovarian germ cell tumour", "Germ cell tumour of ovary", "Ovarian Germ Cell Neoplasm", "ovarian germ cell neoplasm", "germ cell neoplasm of ovary", "germ cell neoplasm of Ovary", "Germ Cell Neoplasm of Ovary", "Germ Cell Tumor of the Ovary", "germ cell tumor of the ovary", "germ cell neoplasm of the ovary", "Germ Cell Neoplasm of the Ovary", "Germ cell tumor of ovary (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian germ cell tumor", "shortest_name_length": 21}
{"curie": "MONDO:0011638", "names": ["NBIA3", "Neuroferritinopathy", "NEUROFERRITINOPATHY", "neuroferritinopathy", "hereditary ferritinopathy", "Hereditary ferritinopathy", "Hereditary Ferritinopathy", "Adult basal ganglia disease", "adult basal ganglia disease", "Neuroferritinopathy (disorder)", "basal ganglia disease adult-onset", "Adult onset basal ganglia disease", "Ferritin-Related Neurodegeneration", "Ferritin related neurodegeneration", "basal ganglia disease, adult-onset", "Basal Ganglia Disease, Adult-Onset", "Ferritin-related neurodegeneration", "BASAL GANGLIA DISEASE, ADULT-ONSET", "ferritin-related neurodegeneration", "Neurodegeneration With Brain Iron Accumulation 3", "neurodegeneration with brain iron accumulation 3", "NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3", "neurodegeneration with brain iron accumulation type 3", "Neuroferritinopathy; basal ganglia disease, adult-onset", "Neuroferritinopathy; Basal Ganglia Disease, Adult-Onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuroferritinopathy", "shortest_name_length": 5}
{"curie": "MONDO:0014593", "names": ["DEE29", "EIEE29", "early infantile epileptic encephalopathy 29", "developmental and epileptic encephalopathy 29", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 29", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 29", "epileptic encephalopathy, early infantile, 29", "AARS early infantile epileptic encephalopathy", "developmental and epileptic encephalopathy, 29", "epileptic encephalopathy, early infantile, type 29", "early infantile epileptic encephalopathy caused by mutation in AARS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 29", "shortest_name_length": 5}
{"curie": "MONDO:0014037", "names": ["SPGF11", "KLHL10 azoospermia", "SPERMATOGENIC FAILURE 11", "spermatogenic failure 11", "spermatogenic failure type 11", "azoospermia caused by mutation in KLHL10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 11", "shortest_name_length": 6}
{"curie": "MONDO:0009714", "names": ["Myosclerosis", "myosclerosis", "Myopathy, Myosclerotic", "MYOPATHY, MYOSCLEROTIC", "myopathy, myosclerotic", "Myosclerosis (disorder)", "myosclerosis, congenital", "MYOSCLEROSIS, AUTOSOMAL RECESSIVE", "myosclerosis, autosomal recessive", "Myosclerosis, Autosomal Recessive", "Congenital myosclerosis Lowenthal type", "Myosclerosis, Congenital, of Lowenthal", "MYOSCLEROSIS, CONGENITAL, OF LOWENTHAL", "myosclerosis, congenital, of Lowenthal", "Congenital myosclerosis, Löwenthal type", "congenital myosclerosis, Löwenthal type", "congenital myosclerosis, LC6wenthal type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myosclerosis", "shortest_name_length": 12}
{"curie": "MONDO:0100255", "names": ["MRT8", "MRT8, FORMERLY", "ADK deficiency", "ADK hypermethioninemia", "adenosine kinase deficiency", "autosomal recessive mental retardation 8", "mental retardation, autosomal recessive 8", "Mental Retardation, Autosomal Recessive 8", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 8", "autosomal recessive intellectual disability 8", "mental retardation, autosomal recessive 8; MRT8", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 8, FORMERLY", "mental retardation, autosomal recessive 8, formerly", "HYPERMETHIONINEMIA DUE TO ADENOSINE KINASE DEFICIENCY", "hypermethioninemia due to adenosine kinase deficiency", "hypermethioninemia encephalopathy due to ADK deficiency", "Hypermethioninemia encephalopathy due to ADK deficiency", "hypermethioninemia encephalopathy due to adenosine kinase deficiency", "Hypermethioninemia encephalopathy due to adenosine kinase deficiency", "Hypermethioninemia encephalopathy due to deficiency of adenosine kinase", "hypermethioninemia encephalopathy due to deficiency of adenosine kinase", "Hypermethioninaemia encephalopathy due to deficiency of adenosine kinase", "Hypermethioninemia encephalopathy due to ADK (adenosine kinase) deficiency", "Hypermethioninaemia encephalopathy due to ADK (adenosine kinase) deficiency", "Hypermethioninemia encephalopathy due to deficiency of adenosine kinase (disorder)", "hypermethioninemia encephalopathy due to deficiency of adenosine kinase (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenosine kinase deficiency", "shortest_name_length": 4}
{"curie": "UMLS:C4288032", "names": ["Skene duct cyst", "Skene Duct Cyst", "Cyst of Skene's duct", "Vaginal Tubulosquamous Polyp", "Cyst of Skene's duct (disorder)", "Vaginal Ectopic Prostatic Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cyst of Skene's duct", "shortest_name_length": 15}
{"curie": "UMLS:C0948348", "names": ["Tumor-Associated Fever", "Tumor associated fever", "Tumor Associated Fever", "Tumour associated fever"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tumor associated fever", "shortest_name_length": 22}
{"curie": "UMLS:C0002897", "names": ["Anemia splenic", "Splenic Anemia", "Anaemia splenic", "Splenic Anemias", "Anemia, Splenic", "splenic; anemia", "anemia; splenic", "Anemias, Splenic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anemia, Splenic", "shortest_name_length": 14}
{"curie": "UMLS:C1333279", "names": ["Descending Colon NET G1", "Descending Colon Carcinoid Tumor", "Carcinoid Tumor of Descending Colon", "Carcinoid Tumor of the Descending Colon", "Descending Colon Neuroendocrine Tumor G1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Descending Colon Neuroendocrine Tumor G1", "shortest_name_length": 23}
{"curie": "MONDO:0005873", "names": ["Neuroaspergillosis", "neuroaspergillosis", "Neuroaspergilloses"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuroaspergillosis", "shortest_name_length": 18}
{"curie": "UMLS:C0751863", "names": ["Adult Neurologic Saturnism", "Plumbism, Neurologic, Adult", "Saturnism, Adult Neurologic", "Neurologic Saturnism, Adult", "Lead Poisoning, Neurologic, Adult", "Poisoning, Lead, Neurologic, Adult", "Neurotoxicity Syndrome, Lead, Adult", "Nervous System Toxicity, Lead, Adult", "Nervous System Poisoning, Lead, Adult", "Lead Poisoning, Nervous System, Adult", "Poisoning, Lead, Nervous System, Adult", "Lead Induced Nervous System Diseases, Adult", "Nervous System Diseases, Lead Induced, Adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lead Poisoning, Nervous System, Adult", "shortest_name_length": 26}
{"curie": "UMLS:C0877334", "names": ["Arterial stenosis limb"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arterial stenosis limb", "shortest_name_length": 22}
{"curie": "MONDO:0700083", "names": ["reciprocal translocation down syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "reciprocal translocation down syndrome", "shortest_name_length": 38}
{"curie": "MONDO:0003445", "names": ["extrahepatic bile duct adenoma", "Extrahepatic Bile Duct Adenoma", "extrahepatic; adenoma bile duct", "adenoma; bile duct, extrahepatic", "bile duct; adenoma, extrahepatic", "adenoma; extrahepatic bile ducts", "adenoma of extrahepatic bile duct", "Adenoma of Extrahepatic Bile Duct", "Adenoma of the Extrahepatic Bile Duct", "adenoma of the extrahepatic bile duct", "adenoma of extrahepatic bile duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extrahepatic bile duct adenoma", "shortest_name_length": 30}
{"curie": "MONDO:0020425", "names": ["abnormal number of coronary ostia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "abnormal number of coronary ostia", "shortest_name_length": 33}
{"curie": "OMIM:605429", "names": ["DFNM1", "DFNB26M", "DFNB26, MODIFIER OF", "DFNB26, SUPPRESSOR OF", "DEAFNESS, NONSYNDROMIC, MODIFIER OF, 1", "DEAFNESS, AUTOSOMAL RECESSIVE 26, MODIFIER OF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 5}
{"curie": "UMLS:C4763867", "names": ["Cirrhosis of the Liver Secondary to Hepatitis C"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cirrhosis of the Liver Secondary to Hepatitis C", "shortest_name_length": 47}
{"curie": "MONDO:0001864", "names": ["residual stage angle-closure glaucoma", "Residual stage angle-closure glaucoma", "Residual stage of angle-closure glaucoma", "residual stage of angle-closure glaucoma", "Residual stage angle-closure glaucoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "residual stage angle-closure glaucoma", "shortest_name_length": 37}
{"curie": "UMLS:C5446422", "names": ["Benign Lacrimal System Neoplasm", "Benign Lacrimal Apparatus Neoplasm", "Benign neoplasm of lacrimal apparatus", "Benign neoplasm of lacrimal apparatus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign neoplasm of lacrimal apparatus", "shortest_name_length": 31}
{"curie": "MONDO:0004410", "names": ["sarcomatoid penile carcinoma", "Sarcomatoid Penile Carcinoma", "sarcomatoid carcinoma of the penis", "Sarcomatous Carcinoma of the Penis", "Sarcomatoid Carcinoma of the Penis", "sarcomatous carcinoma of the penis", "Spindle Cell Carcinoma of the Penis", "spindle cell carcinoma of the penis", "sarcomatoid penile squamous cell carcinoma", "Sarcomatoid Penile Squamous Cell Carcinoma", "squamous cell carcinoma of penis, sarcomatoid type", "Squamous Cell Carcinoma of Penis, Sarcomatoid Type", "squamous cell carcinoma of the penis, sarcomatoid type", "Squamous Cell Carcinoma of the Penis, Sarcomatoid Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sarcomatoid penile squamous cell carcinoma", "shortest_name_length": 28}
{"curie": "UMLS:C5192371", "names": ["GSM", "Genitourinary syndrome of menopause", "Genitourinary Syndrome of Menopause", "Genitourinary syndrome of menopause (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Genitourinary syndrome of menopause", "shortest_name_length": 3}
{"curie": "MONDO:0014967", "names": ["HTX8", "PKD1L1 visceral heterotaxy", "HETEROTAXY, VISCERAL, 8, AUTOSOMAL", "heterotaxy, visceral, 8, autosomal", "heterotaxy, visceral, 8, autosomal; HTX8", "visceral heterotaxy caused by mutation in PKD1L1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heterotaxy, visceral, 8, autosomal", "shortest_name_length": 4}
{"curie": "UMLS:C3897514", "names": ["Stage IVB Oropharyngeal Lymphoepithelioma", "Stage IVB Oropharyngeal Lymphoepithelioma AJCC v7", "Stage IVB Oropharyngeal Undifferentiated Carcinoma", "Stage IVB Undifferentiated Oropharyngeal Throat Cancer", "Stage IVB Oropharyngeal Undifferentiated Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Oropharyngeal Undifferentiated Carcinoma AJCC v7", "shortest_name_length": 41}
{"curie": "UMLS:C5235944", "names": ["Metastatic Dedifferentiated Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Dedifferentiated Liposarcoma", "shortest_name_length": 39}
{"curie": "MONDO:0016294", "names": ["Hirschsprung disease type d brachydactyly", "Hirschsprung disease with type D brachydactyly", "HIRSCHSPRUNG DISEASE WITH TYPE D BRACHYDACTYLY", "Hirschsprung disease with type d brachydactyly", "Hirschsprung Disease with Type D Brachydactyly", "Hirschsprung disease-type D brachydactyly syndrome", "Familial Hirschsprung's disease and type D brachydactyly", "familial Hirschsprung's disease and type D brachydactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hirschsprung disease-type D brachydactyly syndrome", "shortest_name_length": 41}
{"curie": "UMLS:C5420499", "names": ["Advanced Differentiated Thyroid Gland Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Differentiated Thyroid Gland Carcinoma", "shortest_name_length": 47}
{"curie": "UMLS:C5419176", "names": ["COVID-19-Associated Acute Gastrointestinal Tract Injury", "SARS-CoV-2-Associated Acute Gastrointestinal Tract Injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "COVID-19-Associated Acute Gastrointestinal Tract Injury", "shortest_name_length": 55}
{"curie": "UMLS:C4552679", "names": ["Stage I Thyroid Gland Follicular Cancer", "Stage I Thyroid Gland Follicular Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Thyroid Gland Follicular Carcinoma AJCC v8", "shortest_name_length": 39}
{"curie": "UMLS:C4054345", "names": ["Non-Cutaneous Leiomyosarcoma", "Leiomyosarcoma (Excluding Skin)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Cutaneous Leiomyosarcoma", "shortest_name_length": 28}
{"curie": "UMLS:C1332899", "names": ["Cerebellar Glioblastoma", "Glioblastoma of Cerebellum", "Glioblastoma of the Cerebellum", "Cerebellar Glioblastoma Multiforme"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebellar Glioblastoma", "shortest_name_length": 23}
{"curie": "MONDO:0011574", "names": ["Tetralogy Of Fallot Syndrome, Autosomal Recessive", "TETRALOGY OF FALLOT SYNDROME, AUTOSOMAL RECESSIVE", "tetralogy of fallot syndrome, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tetralogy of fallot syndrome, autosomal recessive", "shortest_name_length": 49}
{"curie": "UMLS:C0686112", "names": ["metastatic gallbladder cancer", "Gallbladder cancer metastatic", "Cancer metastatic to gallbladder", "Metastatic Tumor to the Gallbladder", "Metastatic Neoplasm to the Gallbladder", "gallbladder neoplasm malignant secondary", "Secondary malignant neoplasm of gallbladder", "Secondary Malignant Tumor to the Gallbladder", "Metastatic malignant neoplasm to gallbladder", "Metastatic malignant neoplasm of gallbladder", "Secondary Malignant Neoplasm to the Gallbladder", "Metastatic Malignant Neoplasm to the Gallbladder", "Metastatic Malignant Neoplasm in the Gallbladder", "Secondary malignant neoplasm of gallbladder (diagnosis)", "Metastatic malignant neoplasm to gallbladder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Neoplasm to the Gallbladder", "shortest_name_length": 29}
{"curie": "MONDO:0010264", "names": ["AHC", "AHX", "AHCH", "AHC WITH HHG", "AHC with HHG", "X-linked AHC", "X-Linked Addison Disease", "Addison Disease, X-Linked", "Addison Disease, X Linked", "Addison disease, X-linked", "ADDISON DISEASE, X-LINKED", "Primary adrenal hypoplasia", "X-linked Adrenal Hypoplasia", "X linked Adrenal Hypoplasia", "adrenal hypoplasia congenita", "Adrenal Hypoplasia, X-linked", "Adrenal hypoplasia congenita", "Adrenal Hypoplasia Congenita", "Congenital adrenal hypoplasia", "Congenital Adrenal Hypoplasia", "congenital adrenal hypoplasia", "Adrenal hypoplasia, congenital", "Congenital small adrenal gland", "Congenital Adrenal Hypoplasias", "Adrenal Hypoplasia, Congenital", "Hypoplasia, Congenital Adrenal", "adrenal hypoplasia, congenital", "ADRENAL HYPOPLASIA, CONGENITAL", "Familial X linked Addison Disease", "Familial X-linked Addison Disease", "CAH - Congenital adrenal hypoplasia", "Congenital adrenal gland hypoplasia", "Congenital Adrenal Gland Hypoplasia", "Cytomegalic Adrenocortical Hypoplasia", "X-linked adrenal hypoplasia congenita", "X-Linked Adrenal Hypoplasia Congenita", "CYTOMEGALIC ADRENOCORTICAL HYPOPLASIA", "cytomegalic adrenocortical hypoplasia", "mineralocorticoid deficiency, isolated", "X linked Congenital Adrenal Hypoplasia", "Cytomegalic Adrenocortical Hypoplasias", "Congenital hypoplasia of adrenal gland", "X-linked congenital adrenal hypoplasia", "Congenital adrenal hypoplasia syndrome", "X-linked Congenital Adrenal Hypoplasia", "Congenital adrenal hypoplasia, X-linked", "AHC with isolated gonadotropin deficiency", "AHC with Isolated Gonadotropin Deficiency", "AHC WITH ISOLATED GONADOTROPIN DEFICIENCY", "cytomegalic congenital adrenal hypoplasia", "Congenital hypoplasia of adrenal gland (disorder)", "adrenal hypoplasia, congenital, X-linked recessive", "Congenital adrenal hypoplasia, X-linked (disorder)", "adrenal hypoplasia, congenital, with precocious puberty", "Adrenal Hypoplasia, Congenital, with Hypogonadotropic Hypogonadism", "adrenal hypoplasia, congenital, with hypogonadotropic hypogonadism", "ADRENAL HYPOPLASIA, CONGENITAL, WITH HYPOGONADOTROPIC HYPOGONADISM", "adrenal insufficiency, progressive, and hypogonadotropic hypogonadism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked adrenal hypoplasia congenita", "shortest_name_length": 3}
{"curie": "MONDO:0015422", "names": ["OFD13", "OFDS 13", "OFD syndrome 13", "Degner syndrome", "orofaciodigital syndrome 13", "Orofaciodigital Syndrome 13", "orofaciodigital syndrome XIII", "oral facial digital syndrome 13", "oral-facial-digital syndrome 13", "orofaciodigital syndrome type 13", "Orofaciodigital syndrome type 13", "oral-facial-digital syndrome XIII", "Oro-facial digital syndrome type 13", "Oral-facial-digital syndrome type 13", "oral facial digital syndrome type 13", "oral-facial-digital syndrome type 13", "Oro-facial digital syndrome type 13 (disorder)", "oral-facial-digital syndrome type 13 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orofaciodigital syndrome type 13", "shortest_name_length": 5}
{"curie": "MONDO:0018423", "names": ["SPG71", "autosomal recessive spastic paraplegia type 71"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive spastic paraplegia type 71", "shortest_name_length": 5}
{"curie": "MONDO:0015810", "names": ["primary cutaneous CD4+ small/medium-sized pleomorphic T-cell lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary cutaneous CD4+ small/medium-sized pleomorphic T-cell lymphoma", "shortest_name_length": 69}
{"curie": "MONDO:0030897", "names": ["LESKRES", "Lessel-Kreienkamp syndrome", "LESSEL-KREIENKAMP SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lessel-Kreienkamp syndrome", "shortest_name_length": 7}
{"curie": "UMLS:C1610624", "names": ["Stoma Site Infection", "infection stoma site", "Stoma site infection", "infection of stoma site", "infection of stoma site (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stoma Site Infection", "shortest_name_length": 20}
{"curie": "UMLS:C4744408", "names": ["Unresectable Low Grade Glioma", "Unresectable Low-Grade Glioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Low Grade Glioma", "shortest_name_length": 29}
{"curie": "MONDO:0007160", "names": ["AOM", "STL1", "Stickler syndrome", "Stickler Syndrome", "Stickler Dysplasia", "Stickler syndrome 1", "arthro-ophthalmopathy", "Stickler syndrome type 1", "type 1 Stickler syndrome", "Stickler Syndrome Type 1", "Stickler syndrome, type 1", "Stickler Syndrome, Type I", "Stickler syndrome, type I", "STICKLER SYNDROME, TYPE I", "arthro-ophthalmopathy (AO, AOM)", "Hereditary Arthro-Ophthalmopathy", "Hereditary arthro-ophthalmopathy", "hereditary arthro-ophthalmopathy", "arthro-ophthalmopathia hereditaria", "Stickler syndrome, vitreous type 1", "STICKLER SYNDROME, VITREOUS TYPE 1", "Stickler syndrome type 1 (disorder)", "type 1 Stickler syndrome (diagnosis)", "Hereditary Arthro-Ophthalmo-Dystrophy", "Stickler syndrome, membranous vitreous type", "STICKLER SYNDROME, MEMBRANOUS VITREOUS TYPE", "Hereditary progressive arthro-ophthalmopathy", "hereditary progressive arthro-ophthalmopathy", "arthroophthalmopathy, hereditary progressive", "ARTHROOPHTHALMOPATHY, HEREDITARY PROGRESSIVE", "Arthroophthalmopathy, hereditary progressive", "Hereditary progressive arthro-ophthalmopathy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stickler syndrome type 1", "shortest_name_length": 3}
{"curie": "MONDO:0100239", "names": ["inherited hypertrophic pyloric stenosis", "hereditary hypertrophic pyloric stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited hypertrophic pyloric stenosis", "shortest_name_length": 39}
{"curie": "UMLS:C1334317", "names": ["Kadish Stage C Olfactory Neuroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kadish Stage C Olfactory Neuroblastoma", "shortest_name_length": 38}
{"curie": "UMLS:C2936444", "names": ["Pyogenic Sacroiliitis", "Sacroiliitis, Pyogenic", "Pyogenic Sacroiliitides", "Sacroiliitides, Pyogenic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pyogenic Sacroiliitis", "shortest_name_length": 21}
{"curie": "UMLS:C4704910", "names": ["Maternal Sepsis", "Sepsis, Maternal", "Sepsis in Pregnancy", "Sepsis in Pregnancies", "Sepsis during Pregnancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Maternal Sepsis", "shortest_name_length": 15}
{"curie": "UMLS:C0042347", "names": ["varicose veins with inflammation", "varicose veins with inflammation (diagnosis)", "Varicose veins with inflammation of lower extremity", "Varicose veins of lower extremity with inflammation", "Varicose Vein of Lower Extremities with Inflammation", "Varicose veins of lower extremities with inflammation", "Varicose veins with inflammation of any part of lower extremity or of unspecified site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Varicose veins of lower extremities with inflammation", "shortest_name_length": 32}
{"curie": "UMLS:C1336344", "names": ["Stage IVA Larynx Verrucous Carcinoma", "Stage IVA Verrucous Carcinoma of Larynx", "Stage IVA Laryngeal Verrucous Carcinoma", "Stage IVA Verrucous Carcinoma of the Larynx", "Stage IVA Laryngeal Throat Verrucous Cancer", "Stage IVA Laryngeal Verrucous Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Laryngeal Verrucous Carcinoma AJCC v7", "shortest_name_length": 36}
{"curie": "UMLS:C0741026", "names": ["Atypical angina", "ANGINA ATYPICAL", "Atypical Angina", "atypical angina pectoris", "Atypical angina (disorder)", "atypical angina pectoris (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypical angina", "shortest_name_length": 15}
{"curie": "MONDO:0016474", "names": ["DIL", "DILE", "SLE; drug", "drug; SLE", "SECONDARY LUPUS", "Drug Induced Lupus", "drug induced lupus", "DRUG-INDUCED LUPUS", "Drug-Induced Lupus", "lupus drug-induced", "drug-induced lupus", "lupus drug induced", "Lupus-like syndrome", "LUPUS ERYTHEMATOSUS DRUG INDUCED", "Drug Induced Lupus Erythematosus", "drug induced lupus erythematosus", "Drug-induced lupus erythematosus", "drug-induced lupus erythematosus", "Drug-induced lupus erythematosus, NOS", "Drug-induced systemic lupus erythematosus", "drug induced systemic lupus erythematosus", "Drug-induced lupus erythematosus (disorder)", "Drug-induced lupus erythematosus (diagnosis)", "Drug-induced systemic lupus erythematosus (disorder)", "drug induced systemic lupus erythematosus (diagnosis)", "disorders of connective tissue lupus erythematosus drug-induced"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "drug-induced lupus erythematosus", "shortest_name_length": 3}
{"curie": "MONDO:0019926", "names": ["X small rings", "Small ring X chromosome", "Small ring X chromosome (disorder)", "Small ring X chromosome (diagnosis)", "anomaly of chromosome small ring X chromosome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X small rings", "shortest_name_length": 13}
{"curie": "MONDO:0014782", "names": ["LGMD2X", "CARICK", "LGMDR25", "LGMD type 2X", "BVES-related LGMD", "Limb-girdle muscular dystrophy 2X", "Limb girdle muscular dystrophy 2X", "muscular dystrophy, limb-girdle, type 2x", "muscular dystrophy, limb-girdle, type 2X", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2X", "BVES-related limb girdle muscular dystrophy", "BVES-related limb-girdle muscular dystrophy", "BVES autosomal recessive limb-girdle muscular dystrophy", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 25", "CARDIAC ARRHYTHMIA WITH INCREASED SERUM CREATINE KINASE", "muscular dystrophy, limb-girdle, autosomal recessive 25", "autosomal recessive limb-girdle muscular dystrophy type 2X", "Blood vessel epicardial substance related limb girdle muscular dystrophy", "autosomal recessive limb-girdle muscular dystrophy caused by mutation in BVES", "autosomal recessive limb-girdle muscular dystrophy-cardiac arrhythmia syndrome", "Autosomal recessive limb-girdle muscular dystrophy-cardiac arrhythmia syndrome", "Autosomal recessive limb girdle muscular dystrophy, cardiac arrhythmia syndrome", "BVES (blood vessel epicardial substance) related limb girdle muscular dystrophy", "Blood vessel epicardial substance related limb girdle muscular dystrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive limb-girdle muscular dystrophy type 2X", "shortest_name_length": 6}
{"curie": "MONDO:0042924", "names": ["Vagneur Triolle Ripert syndrome", "Vagneur-Triolle-Ripert syndrome", "hypertelorism, short midface, arachnodactyly, coloboma of iris and delayed bone age"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vagneur-Triolle-Ripert syndrome", "shortest_name_length": 31}
{"curie": "MONDO:0011179", "names": ["Tegumentary leishmaniasis susceptibility", "leishmaniasis, tegumentary, susceptibility to", "LEISHMANIASIS, TEGUMENTARY, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leishmaniasis, tegumentary, susceptibility to", "shortest_name_length": 40}
{"curie": "UMLS:C3665888", "names": ["Reproductive toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reproductive toxicity", "shortest_name_length": 21}
{"curie": "UMLS:C4518372", "names": ["PPMS", "Primary Pulmonary Myxoid Sarcoma", "Low-Grade Malignant Myxoid Endobronchial Tumor", "Pulmonary myxoid sarcoma with EWSR1-CREB1 translocation", "Pulmonary Myxoid Sarcoma with EWSR1-CREB1 Translocation", "Primary Pulmonary Myxoid Sarcoma with EWSR1-CREB1 Fusion", "Primary Pulmonary Myxoid Sarcoma with EWSR1::CREB1 Fusion", "Pulmonary myxoid sarcoma with EWSR1-CREB1 translocation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pulmonary myxoid sarcoma with EWSR1-CREB1 translocation", "shortest_name_length": 4}
{"curie": "UMLS:C0347007", "names": ["Metastasis to urinary tract", "Metastases to urinary tract", "Urinary tract metastases NOS", "Cancer metastatic to urinary tract", "malignant neoplasm urinary system secondary", "Metastases to urinary tract unspecified organ", "Secondary malignant neoplasm of urinary system", "Metastatic malignant neoplasm to urinary system", "Metastatic malignant neoplasm of urinary system", "Secondary malignant neoplasm of urinary system, NOS", "Metastatic Malignant Neoplasm in the Urinary System", "Metastatic malignant neoplasm to urinary system, NOS", "Metastatic malignant neoplasm to urinary system (disorder)", "Secondary malignant neoplasm of urinary system (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to urinary system", "shortest_name_length": 27}
{"curie": "MONDO:0010767", "names": ["SPGFY2", "AZF REGIONS", "Azf regions", "AZOOSPERMIA FACTOR REGIONS", "azoospermia Factor regions", "spermatogenic arrest, Y-linked", "SPERMATOGENIC ARREST, Y-LINKED", "Spermatogenic Arrest, Y-Linked", "Y-Linked Spermatogenic Failure-2", "Y-linked spermatogenic failure 2", "spermatogenic failure, Y-linked, 2", "SPERMATOGENIC FAILURE, Y-LINKED, 2", "azoospermia, nonobstructive, Y-linked", "AZOOSPERMIA, NONOBSTRUCTIVE, Y-LINKED", "Azoospermia, Nonobstructive, Y-Linked", "oligospermia, nonobstructive, Y-linked", "Oligospermia, Nonobstructive, Y-Linked", "OLIGOSPERMIA, NONOBSTRUCTIVE, Y-LINKED", "spermatogenic failure, Y-linked, type 2", "OLIGOZOOSPERMIA, NONOBSTRUCTIVE, Y-LINKED", "Oligozoospermia, Nonobstructive, Y-Linked", "oligozoospermia, nonobstructive, Y-linked", "spermatogenic failure, Y-linked, 2, Y-linked", "nonobstructive Y-linked spermatogenic failure", "spermatogenic failure, nonobstructive, Y-linked", "SPERMATOGENIC FAILURE, NONOBSTRUCTIVE, Y-LINKED", "Spermatogenic Failure, Nonobstructive, Y-Linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure, Y-linked, 2", "shortest_name_length": 6}
{"curie": "UMLS:C1881244", "names": ["Teratoid medulloepithelioma", "Intraocular Teratoid Medulloepithelioma", "Ciliary Body Teratoid Medulloepithelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ciliary Body Teratoid Medulloepithelioma", "shortest_name_length": 27}
{"curie": "UMLS:C1112413", "names": ["Peripheral artery aneurysm", "Aneurysm of peripheral artery", "Aneurysm of peripheral arteries", "Aneurysm of peripheral artery (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aneurysm of peripheral artery", "shortest_name_length": 26}
{"curie": "UMLS:C2242485", "names": ["Malacoplakia gastrointestinal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malacoplakia gastrointestinal", "shortest_name_length": 29}
{"curie": "MONDO:0002003", "names": ["Papillitis", "papillitis", "PAPILLITIS", "choked disk", "Papilledema", "Choked disc", "Choked disk", "disk choked", "PAPILLEDEMA", "Choked Disk", "papilledema", "choked discs", "Papilloedema", "Disk, Choked", "PAPILLOEDEMA", "papilloedema", "Choked Disks", "Papillitis NOS", "OPTIC PAPILLITIS", "Optic Disk Edema", "PAPILLITIS OPTIC", "Optic Papillitis", "optic papillitis", "Optic Disc Edema", "Optic disc edema", "Papillitis optic", "OPTIC DISC EDEMA", "optic disc edema", "Optic papillitis", "Papilledema, NOS", "Edema, Optic Disc", "optic; papillitis", "Papillitis, Optic", "Optic disc oedema", "papillitis; optic", "Edema, Optic Disk", "Edemas, Optic Disc", "Optic disc swollen", "Edemas, Optic Disk", "swollen optic disc", "Optic disc swelling", "OPTIC DISCS BLURRED", "Edema of optic disc", "Optic discs blurred", "Optic Papilla Edema", "optic disc swelling", "Edema, Optic Papilla", "Blurring of optic disk", "Blurring of optic disc", "Optic Nerve Papillitis", "Optic disc engorgement", "Optic disc inflammation", "disc inflammation optic", "papilledema (diagnosis)", "Papillitis, Optic Nerve", "Unspecified papilledema", "Edema of the Optic Disk", "edema of the optic disc", "Edema of the Optic Disc", "Papilledema, unspecified", "Papilloedema, unspecified", "Optic papillitis (disorder)", "Disc edema in ocular fundus", "Disc oedema in ocular fundus", "optic papillitis (diagnosis)", "Optic disc swelling (finding)", "Edema of optic disc (disorder)", "papilledema (physical finding)", "Disc congestion in ocular fundus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papilledema", "shortest_name_length": 10}
{"curie": "MONDO:0023305", "names": ["metal poison", "metal poisons", "metal poisoning", "Metal poisoning", "heavy metal poison", "heavy metal poisons", "heavy metal toxicity", "Metal poisoning, NOS", "Heavy metal poisoning", "HEAVY METAL POISONING", "heavy metal poisoning", "Heavy Metal Poisoning", "heavy metal toxicosis", "heavy metal poisonings", "Toxic effect of metals", "heavy metals poisoning", "Heavy Metal Poisonings", "Poisoning, Heavy Metal", "Metal Poisoning, Heavy", "Metal Poisonings, Heavy", "Poisonings, Heavy Metal", "poisoning by heavy metals", "Heavy metal poisoning, NOS", "Metal causing toxic effect", "toxic effect of heavy metal", "Toxic effect of heavy metal", "Toxic effect of other metals", "Toxic effects of other metals", "chronic heavy metal poisoning", "Heavy metal poisoning syndrome", "Toxic effect of other metal, NOS", "Toxic effect of heavy metal, NOS", "Toxic effects of other metals NOS", "poisoning by heavy metals (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heavy metal poisoning", "shortest_name_length": 12}
{"curie": "MONDO:0005184", "names": ["PDA", "PDAC", "pancreatic duct cancer", "Pancreatic Ductal Carcinoma", "pancreatic ductal carcinoma", "Pancreas Duct-Cell Carcinoma", "Pancreatic Ductal Carcinomas", "Carcinoma, Pancreatic Ductal", "Ductal Carcinoma, Pancreatic", "Carcinoma, Pancreas Duct-Cell", "Duct Cell Carcinoma, Pancreas", "Carcinomas, Pancreatic Ductal", "Duct-Cell Carcinoma, Pancreas", "Ductal Carcinomas, Pancreatic", "Pancreas Duct-Cell Carcinomas", "Carcinoma, Ductal, Pancreatic", "Pancreatic Duct Cell Carcinoma", "Duct-Cell Carcinomas, Pancreas", "Carcinomas, Pancreas Duct-Cell", "pancreas ductal adenocarcinoma", "Pancreas Ductal Adenocarcinoma", "pancreatic duct adenocarcinoma", "Ductal Carcinoma of the Pancreas", "pancreatic ductal adenocarcinoma", "Pancreatic Ductal Adenocarcinoma", "Pancreatic ductal adenocarcinoma", "Adenocarcinoma of pancreatic duct", "Ductal adenocarcinoma of pancreas", "Ductal Adenocarcinoma of Pancreas", "pancreatic tubular adenocarcinoma", "ductal adenocarcinoma of pancreas", "Pancreatic Tubular Adenocarcinoma", "Malignant tumor of pancreatic duct", "Malignant tumour of pancreatic duct", "Duct Cell Carcinoma of the Pancreas", "Duct-Cell Carcinoma of the Pancreas", "malignant neoplasm of duct of Wirsung", "adenocarcinoma, duct cell, pancreatic", "ductal adenocarcinoma of the pancreas", "Malignant neoplasm of pancreatic duct", "Malignant neoplasm of duct of Wirsung", "malignant neoplasm of pancreatic duct", "Ductal Adenocarcinoma of the Pancreas", "PDAC - pancreatic ductal adenocarcinoma", "duct cell adenocarcinoma of the pancreas", "pancreas cancer, duct cell adenocarcinoma", "pancreatic cancer, duct cell adenocarcinoma", "Pancreatic Infiltrating Duct Carcinoma, NOS", "Adenocarcinoma of pancreatic duct (disorder)", "Malignant tumor of pancreatic duct (disorder)", "pancreatic neoplasm malignant pancreatic duct", "malignant neoplasm of pancreatic duct (diagnosis)", "Pancreatic Infiltrating Duct Carcinoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic ductal adenocarcinoma", "shortest_name_length": 3}
{"curie": "UMLS:C4046002", "names": ["Research-Related Injury", "Injury, Research-Related", "Research-Related Injuries", "Research Related Injuries", "Injuries, Research-Related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Research-Related Injuries", "shortest_name_length": 23}
{"curie": "UMLS:C4526981", "names": ["Stage IV Small Intestinal, Esophageal, Colorectal, Mesenteric, and Peritoneal GIST AJCC v8", "Stage IV Small Intestinal, Esophageal, Colorectal, Mesenteric, and Peritoneal Gastrointestinal Stromal Tumor (GIST)", "Stage IV Small Intestinal, Esophageal, Colorectal, Mesenteric, and Peritoneal Gastrointestinal Stromal Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Small Intestinal, Esophageal, Colorectal, Mesenteric, and Peritoneal Gastrointestinal Stromal Tumor AJCC v8", "shortest_name_length": 90}
{"curie": "UMLS:C0495958", "names": ["lower leg injury", "injury leg lower", "Lower Leg Injury", "injuries leg lower", "Injury of lower leg", "injury of lower leg", "LOWER LEG INJURY TRAUMA", "Injury of lower leg (disorder)", "Unspecified injury of lower leg", "injury of lower leg (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of lower leg", "shortest_name_length": 16}
{"curie": "MONDO:0018642", "names": ["NIK deficiency", "MAP3K14 non-severe combined immunodeficiency", "non-severe combined immunodeficiency caused by mutation in MAP3K14", "primary immunodeficiency with multifaceted aberrant lymphoid immunity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "NIK deficiency", "shortest_name_length": 14}
{"curie": "MONDO:0017044", "names": ["adult familial nephronophthisis-spastic quadriparesia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult familial nephronophthisis-spastic quadriparesia syndrome", "shortest_name_length": 62}
{"curie": "MONDO:0035930", "names": ["3-phosphoserine phosphatase deficiency, prenatal form", "neu-laxova syndrome due to 3-phosphoserine phosphatase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neu-laxova syndrome due to 3-phosphoserine phosphatase deficiency", "shortest_name_length": 53}
{"curie": "UMLS:C0684964", "names": ["Metastatic Tumor to the Hypopharynx", "Metastatic Neoplasm to the Hypopharynx", "Secondary malignant neoplasm of hypopharynx", "hypopharyngeal neoplasm malignant secondary", "Metastatic malignant neoplasm to hypopharynx", "Metastatic malignant neoplasm of hypopharynx", "Metastatic Malignant Neoplasm in the Hypopharynx", "Metastatic Malignant Neoplasm to the Hypopharynx", "Secondary malignant neoplasm of hypopharynx, NOS", "Metastatic malignant neoplasm to hypopharynx, NOS", "Secondary malignant neoplasm of hypopharynx (diagnosis)", "Metastatic malignant neoplasm to hypopharynx (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to hypopharynx", "shortest_name_length": 35}
{"curie": "MONDO:0006418", "names": ["Small Intestinal EATL", "small intestinal EATL", "small intestinal enteropathy-type T-cell lymphoma", "Small Intestinal Enteropathy-Type T-Cell Lymphoma", "small intestine enteropathy-associated T-cell lymphoma", "small intestinal enteropathy-associated T-cell lymphoma", "Small Intestinal Enteropathy-Associated T-Cell Lymphoma", "enteropathy-associated T-cell lymphoma of small intestine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small intestinal enteropathy-associated T-cell lymphoma", "shortest_name_length": 21}
{"curie": "MONDO:0019768", "names": ["X-linked intellectual disability, Golabi-Ito-hall type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability, Golabi-Ito-hall type", "shortest_name_length": 54}
{"curie": "MONDO:0012783", "names": ["CDGIN", "CDG1N", "CDGIn", "CDG-In", "CDG In", "CDG in", "RFT1-CDG", "RFT1-CDG (CDG-In)", "CDG syndrome type In", "Man5GlcNAc2-PP-Dol flippase deficiency", "congenital disorder of glycosylation 1n", "congenital disorder of glycosylation In", "RFT1-congenital disorder of glycosylation", "Congenital disorder of glycosylation type In", "Congenital disorder of glycosylation type 1n", "congenital disorder of glycosylation type In", "congenital disorder of glycosylation type 1n", "Congenital Disorder Of Glycosylation, Type In", "congenital disorder of glycosylation, type In", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE In", "RFT1-CDG (congenital disorder of glycosylation)", "Carbohydrate deficient glycoprotein syndrome type In", "carbohydrate deficient glycoprotein syndrome type In", "Man5GlcNAc2-dolichylpyrophosphate flippase deficiency", "Congenital disorder of glycosylation type 1n (disorder)", "Congenital disorder of glycosylation type In (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "RFT1-congenital disorder of glycosylation", "shortest_name_length": 5}
{"curie": "MONDO:0012067", "names": ["ASRT2", "asthma, susceptibility to, 2", "NPSR1 inherited susceptibility to asthma", "asthma-related traits, susceptibility to, 2", "ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 2", "asthma-related traits, susceptibility to, type 2", "inherited susceptibility to asthma caused by mutation in NPSR1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "asthma-related traits, susceptibility to, 2", "shortest_name_length": 5}
{"curie": "UMLS:C0520767", "names": ["Staphylococcal endocarditis", "Endocarditis staphylococcal", "Staphylococcal endocarditis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Staphylococcal endocarditis", "shortest_name_length": 27}
{"curie": "UMLS:C1336479", "names": ["Stage I Retinoblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Retinoblastoma", "shortest_name_length": 22}
{"curie": "MONDO:0004270", "names": ["Ductal Adenoma", "ductal adenoma", "breast ductal adenoma", "Breast Ductal Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast ductal adenoma", "shortest_name_length": 14}
{"curie": "UMLS:C1333430", "names": ["EBV-Related Hodgkin Lymphoma", "EBV Related Hodgkin's Lymphoma", "EBV-Related Hodgkin's Lymphoma", "Epstein-Barr Virus-Related Hodgkin Lymphoma", "Epstein-Barr Virus-Related Hodgkin's Lymphoma", "Epstein-Barr Virus Related Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "EBV-Related Hodgkin Lymphoma", "shortest_name_length": 28}
{"curie": "MONDO:0003382", "names": ["Eyelid Disease", "eyelid disease", "Disease, Eyelid", "eyelid diseases", "Eyelid Diseases", "disorder eyelid", "Eyelid disorder", "eyelid disorder", "Eyelid Disorder", "Diseases, Eyelid", "eyelid; disorder", "disorders eyelid", "Eyelid Disorders", "disease of eyelid", "Eyelids--Diseases", "eyelids disorders", "DISEASE OF EYELID", "diseases eyelid of", "disorder of eyelid", "Disorder of eyelid", "Eyelid disorder NOS", "Disorder of eyelid NOS", "Disorder of eyelid, NOS", "DISORDERS OF THE EYELIDS", "eyelid disease or disorder", "eyelid disorder (diagnosis)", "Disorder of eyelid (disorder)", "disease or disorder of eyelid", "Unspecified disorder of eyelid", "Disorder of eyelid, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eyelid disorder", "shortest_name_length": 14}
{"curie": "MONDO:0016933", "names": ["partial trisomy/tetrasomy of chromosome 12p", "partial duplication/triplication of chromosome 12p", "partial trisomy/tetrasomy of the short arm of chromosome 12", "partial trisomy/tetrasomy of the short arm of chromosome type 12", "partial duplication/triplication of the short arm of chromosome 12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial trisomy/tetrasomy of the short arm of chromosome 12", "shortest_name_length": 43}
{"curie": "MONDO:0032853", "names": ["MPD6", "myopathy, distal, 6, adult onset", "myopathy, distal, 6, adult-onset, autosomal dominant", "MYOPATHY, DISTAL, 6, ADULT-ONSET, AUTOSOMAL DOMINANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy, distal, 6, adult-onset, autosomal dominant", "shortest_name_length": 4}
{"curie": "UMLS:C4329684", "names": ["Congenital Testicular Failure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Testicular Failure", "shortest_name_length": 29}
{"curie": "MONDO:0013010", "names": ["DFNB71", "autosomal recessive deafness 71", "Deafness, Autosomal Recessive 71", "deafness, autosomal recessive 71", "DEAFNESS, AUTOSOMAL RECESSIVE 71", "autosomal recessive nonsyndromic deafness 71", "autosomal recessive nonsyndromic hearing loss 71", "autosomal recessive nonsyndromic deafness type 71"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 71", "shortest_name_length": 6}
{"curie": "MONDO:0032656", "names": ["MCIDDS", "MICROCEPHALY, CATARACTS, IMPAIRED INTELLECTUAL DEVELOPMENT, AND DYSTONIA WITH ABNORMAL STRIATUM", "microcephaly, cataracts, impaired intellectual development, and dystonia with abnormal striatum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly, cataracts, impaired intellectual development, and dystonia with abnormal striatum", "shortest_name_length": 6}
{"curie": "MONDO:0009184", "names": ["Epidermolysis Bullosa With Diaphragmatic Hernia", "epidermolysis bullosa with diaphragmatic hernia", "EPIDERMOLYSIS BULLOSA WITH DIAPHRAGMATIC HERNIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolysis bullosa with diaphragmatic hernia", "shortest_name_length": 47}
{"curie": "MONDO:0003796", "names": ["rectal Kaposi sarcoma", "Rectal Kaposi Sarcoma", "rectum Kaposi sarcoma", "rectal Kaposi's sarcoma", "rectum Kaposi's sarcoma", "Rectal Kaposi's Sarcoma", "Kaposi sarcoma of rectum", "Kaposi's sarcoma of rectum", "Kaposi's Sarcoma of Rectum", "Kaposi's Sarcoma of the Rectum", "Kaposi's sarcoma of the rectum", "rectum Kaposi's sarcoma (disease)", "Kaposi sarcoma of rectum (disorder)", "Kaposi's sarcoma (disease) of rectum", "Kaposi's sarcoma of rectum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rectum Kaposi sarcoma", "shortest_name_length": 21}
{"curie": "UMLS:C3640084", "names": ["Facial Nerve Palsy due to Trauma", "Facial Nerve Palsy Related to Trauma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Facial Nerve Palsy Related to Trauma", "shortest_name_length": 32}
{"curie": "UMLS:C4527161", "names": ["Cutaneous Melanoma by AJCC v8 Clinical Stage", "Melanoma of the Skin by AJCC v8 Clinical Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous Melanoma by AJCC v8 Clinical Stage", "shortest_name_length": 44}
{"curie": "MONDO:0044917", "names": ["T-Lymphoblastic lymphoma", "T Lymphoblastic Lymphoma", "T-Lymphoblastic Lymphoma", "T-lymphoblastic lymphoma", "T Lymphoblastic lymphoma", "Precur. T-lymphoblastic lymphoma", "precursor T-Lymphoblastic lymphoma", "Precursor T Lymphoblastic Lymphoma", "Precursor T-lymphoblastic lymphoma", "Precursor T-Lymphoblastic Lymphoma", "precursor T Lymphoblastic lymphoma", "precursor T-lymphoblastic lymphoma", "Precursor T-Cell Lymphoblastic Lymphoma", "precursor T-cell Lymphoblastic lymphoma", "Precursor T-cell lymphoblastic lymphoma", "malignant precursor T-cell lymphoblastic lymphoma", "Precursor T-cell lymphoblastic lymphoma (disorder)", "malignant precursor T-cell lymphoblastic lymphoma (diagnosis)", "Precursor T-cell lymphoblastic lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-lymphoblastic lymphoma", "shortest_name_length": 24}
{"curie": "MONDO:0033200", "names": ["DFNB108", "deafness, autosomal recessive 108", "DEAFNESS, AUTOSOMAL RECESSIVE 108", "hearing loss, autosomal recessive 108", "autosomal recessive nonsyndromic deafness 108"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal recessive 108", "shortest_name_length": 7}
{"curie": "MONDO:0013511", "names": ["TNCY", "cyanosis, transient neonatal", "CYANOSIS, TRANSIENT NEONATAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cyanosis, transient neonatal", "shortest_name_length": 4}
{"curie": "UMLS:C0023105", "names": ["Latent schizophrenia", "Latent Schizophrenia", "latent schizophrenia", "Schizophrenia, Latent", "Latent Schizophrenias", "schizophrenia; latent", "latent; schizophrenic", "Schizophrenias, Latent", "Schizophrenia, latent type", "latent schizophrenic reaction", "Latent schizophrenic reaction", "Latent schizophrenia (disorder)", "reaction; schizophrenic, latent", "schizophrenic; reaction, latent", "latent schizophrenia (diagnosis)", "Latent schizophrenia, unspecified", "Latent schizophrenia, unspecified state"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Schizophrenia, Latent", "shortest_name_length": 20}
{"curie": "MONDO:0008949", "names": ["Muller Barth Menger syndrome", "Cerebral malformation, seizures, hypertrichosis, and overlapping fingers", "cerebral malformation, seizures, hypertrichosis, and overlapping fingers", "CEREBRAL MALFORMATION, SEIZURES, HYPERTRICHOSIS, AND OVERLAPPING FINGERS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral malformation, seizures, hypertrichosis, and overlapping fingers", "shortest_name_length": 28}
{"curie": "MONDO:0010505", "names": ["SHLTS", "SCHOLTE syndrome", "SCHOLTE SYNDROME", "Scholte syndrome", "Scholte-Begeer-van Essen syndrome", "Scholte Begeer-van Essen syndrome", "Early balding, patella luxation, acromicria and hypogonadism", "early balding, patella luxation, acromicria and hypogonadism", "EARLY BALDING, PATELLA LUXATION, ACROMICRIA, AND HYPOGONADISM", "early balding, patella luxation, acromicria, and hypogonadism", "Early Balding, Patella Luxation, Acromicria, And Hypogonadism", "Intellectual disability-balding-patella luxation-acromicria syndrome", "intellectual disability-balding-patella luxation-acromicria syndrome", "intellectual disability, balding, patella luxation, acromicria syndrome", "Intellectual disability, balding, patella luxation, acromicria syndrome", "Intellectual disability, balding, patella luxation, acromicria syndrome (disorder)", "intellectual disability, balding, patella luxation, acromicria syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability-balding-patella luxation-acromicria syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0017318", "names": ["PPv", "phakomatosis pigmentovascularis", "Phacomatosis pigmentovascularis", "Phakomatosis pigmentovascularis", "Port-wine stain with oculocutaneous melanosis", "port-wine stain with oculocutaneous melanosis", "Port-wine stain with oculocutaneous melanosis (disorder)", "association of cutaneous vascular malformations and different pigmentary disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phakomatosis pigmentovascularis", "shortest_name_length": 3}
{"curie": "MONDO:0000543", "names": ["ovarian melanoma", "Ovarian Melanoma", "Ovarian melanoma", "ovary melanoma (disease)", "ovary metastatic melanoma", "melanoma (disease) of ovary", "metastatic melanoma of ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian melanoma", "shortest_name_length": 16}
{"curie": "MONDO:0022823", "names": ["congenital contractures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital contractures", "shortest_name_length": 23}
{"curie": "UMLS:C3494248", "names": ["Organothiophosphate Poisoning", "Organothiophosphate Poisonings", "Poisoning, Organothiophosphate", "Poisonings, Organothiophosphate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Organothiophosphate Poisoning", "shortest_name_length": 29}
{"curie": "MONDO:0011088", "names": ["CMS1A", "CMS IIa", "Cms IIa", "CMS2A, FORMERLY", "Cms IIa, formerly", "CMS IIa, FORMERLY", "congenital myasthenic syndrome 1A", "CHRNA1 congenital myasthenic syndrome", "congenital myasthenic syndrome type 1A", "congenital myasthenic syndrome type IIa", "myasthenic syndrome, congenital, type IIa", "congenital myasthenic syndrome 1A, slow-channel", "myasthenic syndrome, congenital, 1A, slow-channel", "MYASTHENIC SYNDROME, CONGENITAL, 1A, SLOW-CHANNEL", "myasthenic syndrome, congenital, type IIa, formerly", "MYASTHENIC SYNDROME, CONGENITAL, TYPE IIa, FORMERLY", "congenital myasthenic syndrome caused by mutation in CHRNA1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myasthenic syndrome 1A", "shortest_name_length": 5}
{"curie": "MONDO:0006432", "names": ["stromal predominant Wilms tumor", "Stromal Predominant Wilms Tumor", "stromal predominant Wilm's tumor", "Wilms tumor, stromal predominant", "stromal predominant Wilms' tumor", "Wilms' tumor, stromal predominant", "Wilm's tumor, stromal predominant", "stromal predominant nephroblastoma", "Stromal Predominant Nephroblastoma", "Stromal Predominant Renal Wilms Tumor", "stromal predominant renal Wilms tumor", "Stromal Predominant renal Wilms tumor", "stromal predominant renal adenosarcoma", "stromal predominant renal Wilms' tumor", "stromal predominant renal Wilm's tumor", "Stromal Predominant Renal Adenosarcoma", "Stromal Predominant Renal Wilm's Tumor", "Stromal Predominant Renal Wilms' Tumor", "Stromal Predominant Kidney Wilms Tumor", "stromal predominant kidney Wilms tumor", "Stromal Predominant renal Wilms tumour", "stromal predominant kidney Wilms' tumor", "Stromal Predominant Kidney Adenosarcoma", "stromal predominant kidney adenosarcoma", "stromal predominant kidney Wilms' tumour"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stromal predominant kidney Wilms tumor", "shortest_name_length": 31}
{"curie": "MONDO:0030539", "names": ["CCHS3", "central hypoventilation syndrome, congenital, 3", "CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central hypoventilation syndrome, congenital, 3", "shortest_name_length": 5}
{"curie": "UMLS:C1336242", "names": ["Stage III Ampullary Carcinoma", "Stage III Ampulla of Vater Cancer", "Ampulla of Vater Cancer Stage III", "Stage III Ampulla of Vater Carcinoma", "Stage III Ampulla of Vater Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Ampulla of Vater Cancer AJCC v7", "shortest_name_length": 29}
{"curie": "UMLS:C1336476", "names": ["Stage I Mesothelioma", "stage I pleural mesothelioma", "Stage I Mesothelioma of Pleura", "stage I mesothelioma of pleura", "stage I malignant mesothelioma", "Stage I Mesothelioma of the Pleura", "stage I mesothelioma of the pleura", "stage I pleural mesothelioma AJCC v7", "Stage I Pleural Malignant Mesothelioma", "Stage I Pleural Malignant Mesothelioma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Pleural Malignant Mesothelioma AJCC v7", "shortest_name_length": 20}
{"curie": "UMLS:C0346218", "names": ["Tumor of glans penis", "Tumour of glans penis", "Neoplasm of glans penis", "neoplasm of the glans penis", "penile neoplasm glans penis", "Neoplasm of glans penis (disorder)", "neoplasm of the glans penis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplasm of glans penis", "shortest_name_length": 20}
{"curie": "MONDO:0035776", "names": ["combined deficiency of factor VII and factor X"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined deficiency of factor VII and factor X", "shortest_name_length": 46}
{"curie": "MONDO:0013966", "names": ["CPVT4", "CVPT4", "catecholaminergic polymorphic ventricular tachycardia 4", "ventricular tachycardia, catecholaminergic polymorphic, 4", "VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 4", "CALM1 catecholaminergic polymorphic ventricular tachycardia", "catecholaminergic polymorphic ventricular tachycardia type 4", "ventricular tachycardia, catecholaminergic polymorphic, type 4", "catecholaminergic polymorphic ventricular tachycardia caused by mutation in CALM1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "catecholaminergic polymorphic ventricular tachycardia 4", "shortest_name_length": 5}
{"curie": "UMLS:C0263324", "names": ["Erythema toxicum", "erythema toxicum", "Erythema neonatorum", "erythema neonatorum", "erythema; neonatorum", "neonatorum; erythema", "Neonatal erythroderma", "Erythroderma neonatorum", "Neonatal toxic erythema", "Neonatal Toxic Erythema", "neonatorum; erythroderma", "erythroderma; neonatorum", "Neonatal Erythema Toxicum", "Toxic erythema of newborn", "Neonatal erythema toxicum", "Erythema Toxicum Neonatorum", "erythema neonatorum toxicum", "erythema toxicum neonatorum", "Erythema toxicum neonatorum", "erythema; neonatorum, toxic", "erythema toxicum of newborn", "Toxic erythema of the newborn", "erythema; toxic, toxic, newborn", "Neonatal erythroderma (disorder)", "ETN - Erythema toxicum neonatorum", "ETN - erythema toxicum neonatorum", "Neonatal toxic erythema (disorder)", "erythema toxicum of newborn (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Erythema toxicum neonatorum", "shortest_name_length": 16}
{"curie": "MONDO:0010665", "names": ["WTS", "MRXS6", "MRXSWT", "Vasquez syndrome", "Wilson-Turner syndrome", "Wilson Turner syndrome", "Wilson-Turner syndrome (WTS)", "Wilson Turner syndrome (disorder)", "Wilson-Turner syndrome (diagnosis)", "X-linked mental retardation syndrome 6", "Wilson Turner mental retardation syndrome", "MENTAL RETARDATION, X-LINKED, SYNDROMIC 6", "mental retardation, X-linked, syndromic 6", "Mental retardation, X-linked, syndromic 6", "Wilson-Turner syndrome, X-linked recessive", "X-linked mental retardation syndrome 6 (MRXS6)", "intellectual disability, X-linked, syndromic 6", "mental retardation-gynecomastia-obesity syndrome", "WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME", "Wilson-TURNER X-linked mental retardation syndrome", "Wilson-Turner X-linked mental retardation syndrome", "mental retardation, X-linked, syndromic 6 (formerly)", "Wilson Turner mental retardation syndrome (formerly)", "Wilson-TURNER X-linked intellectual disability syndrome", "Wilson Turner intellectual disability syndrome (formerly)", "X-linked intellectual disability - gynecomastia - obesity", "intellectual disability, X-linked, syndromic 6 (formerly)", "Mental retardation, X-linked, with gynecomastia and obesity", "MENTAL RETARDATION, X-LINKED, WITH GYNECOMASTIA AND OBESITY", "mental retardation, X-linked, with gynecomastia and obesity", "X-linked intellectual disability-gynecomastia-obesity syndrome", "intellectual disability, X-linked, with gynecomastia and obesity", "mental retardation, X-linked, with gynecomastia and obesity (formerly)", "intellectual disability, X-linked, with gynecomastia and obesity (formerly)", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, WILSON-TURNER TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wilson-Turner syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C4527165", "names": ["Stage IB Cutaneous (Skin) Melanoma", "Clinical Stage IB Cutaneous Melanoma AJCC v8", "Clinical Stage IB Melanoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage IB Cutaneous Melanoma AJCC v8", "shortest_name_length": 34}
{"curie": "MONDO:0007179", "names": ["autoimmunity", "Autoimmunity", "autoimmunities", "Autoimmunities", "Autoimmune state", "Autoimmunity, NOS", "Autoimmune Status", "Autoimmune disease", "Autoimmune Disease", "autoimmune disease", "AUTOIMMUNE DISEASE", "autoimmune diseases", "Disease, Autoimmune", "Autoimmune Diseases", "Autoimmune diseases", "disease, autoimmune", "AUTOIMMUNE DISORDER", "Autoimmune Disorder", "autoimmune disorder", "Autoimmune disorder", "Autoimmune condition", "Autoimmune_condition", "Autoimmune disorders", "Diseases, Autoimmune", "autoimmune disorders", "Autoimmune Disorders", "Autoimmune state, NOS", "autoimmune disease NOS", "Autoimmune disease NOS", "AUTOIMMUNE DISORDER NOS", "Autoimmune disorder NOS", "Autoimmune disease, NOS", "Autoimmune disorder, NOS", "self recognition (immune)", "Autoimmune state (finding)", "Autoimmune disease flare up", "Autoimmune disease (disorder)", "autoimmune disease (diagnosis)", "autoimmune disease or disorder", "autoimmune hypersensitivity disease", "type II hypersensitivity reaction disease", "hypersensitivity reaction type II disease", "Ankylosing spondylitis and other inflammatory spondylopathies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune disease", "shortest_name_length": 12}
{"curie": "MONDO:0018106", "names": ["xanthinuria", "classic xanthinuria", "xanthic urolithiasis", "hereditary xanthinuria", "xanthine stone disease", "xanthine oxidase deficiency", "xanthine dehydrogenase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary xanthinuria", "shortest_name_length": 11}
{"curie": "UMLS:C0280478", "names": ["nonmetastatic GTT", "Non-Metastatic GTT", "non-metastatic GTT", "GTT, non-metastatic", "trophoblastic tumor, non-metastatic", "Nonmetastatic Gestational Trophoblastic Tumor", "nonmetastatic gestational trophoblastic tumor", "Non-Metastatic Gestational Trophoblastic Tumor", "non-metastatic gestational trophoblastic tumor", "gestational trophoblastic tumor, non-metastatic", "Non-Metastatic Gestational Trophoblastic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Metastatic Gestational Trophoblastic Tumor", "shortest_name_length": 17}
{"curie": "MONDO:0015773", "names": ["fibular dimelia-diplopodia syndrome", "Fibular dimelia diplopodia syndrome", "Fibular dimelia-diplopodia syndrome", "Leg duplication mirror foot syndrome", "leg duplication-mirror foot syndrome", "Leg duplication-mirror foot syndrome", "Fibular dimelia diplopodia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibular dimelia-diplopodia syndrome", "shortest_name_length": 35}
{"curie": "MONDO:0019854", "names": ["thyroid ectopia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid ectopia", "shortest_name_length": 15}
{"curie": "DOID:0050537", "names": ["posterior polar cataract", "CATARACT, POSTERIOR POLAR"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "posterior polar cataract", "shortest_name_length": 24}
{"curie": "UMLS:C0240872", "names": ["RECTAL FISSURE", "Rectal fissure", "rectal fissure", "fissure rectal", "fissures rectal", "rectal fissure (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rectal fissure", "shortest_name_length": 14}
{"curie": "MONDO:0003054", "names": ["Meningioma", "Benign Meningioma", "benign meningioma", "Benign meningioma", "Meningioma benign", "Meningioma, Benign", "meningioma, benign", "Benign Meningiomas", "MENINGIOMA, BENIGN", "Meningiomas benign", "benign meningiomas", "Meningiomas, Benign", "Benign meningioma (disorder)", "meningioma (disease), benign", "Benign Meningioma (WHO Grade 1)", "Benign Meningioma (WHO Grade I)", "benign meningioma (WHO grade I)", "Benign meningioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign meningioma", "shortest_name_length": 10}
{"curie": "UMLS:C0862335", "names": ["Recurrent Bladder Urothelial Cancer", "Urothelial carcinoma bladder recurrent", "Recurrent Bladder Urothelial Carcinoma", "Recurrent Bladder Transitional Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urothelial carcinoma bladder recurrent", "shortest_name_length": 35}
{"curie": "UMLS:C0022823", "names": ["Acquired postural kyphosis", "Acquired Postural Kyphosis", "Kyphosis (acquired) (postural)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired postural kyphosis", "shortest_name_length": 26}
{"curie": "MONDO:0033481", "names": ["SCA46", "spinocerebellar ataxia 46", "SPINOCEREBELLAR ATAXIA 46", "Spinocerebellar ataxia type 46", "SPINOCEREBELLAR ATAXIA, 46, AUTOSOMAL DOMINANT, WITH SENSORY AXONAL NEUROPATHY", "spinocerebellar ataxia, 46, autosomal dominant, with sensory axonal neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia 46", "shortest_name_length": 5}
{"curie": "EFO:1001893", "names": ["Hand-foot syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hand-foot syndrome", "shortest_name_length": 18}
{"curie": "MONDO:0044626", "names": ["female infertility due to oocyte meiotic arrest"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "female infertility due to oocyte meiotic arrest", "shortest_name_length": 47}
{"curie": "UMLS:C1333743", "names": ["Gallbladder Metaplastic Polyp", "Gallbladder Hyperplastic Polyp", "Hyperplastic Polyp of Gallbladder", "Hyperplastic Polyp of the Gallbladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gallbladder Hyperplastic Polyp", "shortest_name_length": 29}
{"curie": "UMLS:C0558354", "names": ["Palate Carcinoma", "Palate carcinoma", "carcinoma of palate", "Carcinoma of Palate", "Carcinoma of the Palate", "Palate carcinoma (disorder)", "carcinoma of palate (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Palate carcinoma", "shortest_name_length": 16}
{"curie": "MONDO:0016989", "names": ["FHI", "Fuchs uveitis syndrome", "Fuchs heterochromic uveitis", "Fuchs heterochromic cyclitis", "Fuchs' heterochromic uveitis", "heterochromic cyclitis; Fuchs", "Fuchs' heterochromic cyclitis", "Fuchs; heterochromic cyclitis", "Fuchs heterochromic iridocyclitis", "Fuchs' heterochromic iridocyclitis", "Fuch's heterochromic iridocyclitis", "Fuch's Heterochromic iridocyclitis", "Fuchs' heterochromic cyclitis (disorder)", "Fuchs' heterochromic cyclitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fuchs heterochromic iridocyclitis", "shortest_name_length": 3}
{"curie": "UMLS:C2698878", "names": ["Intestinal Follicular Lymphoma", "Primary Intestinal Follicular Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal Follicular Lymphoma", "shortest_name_length": 30}
{"curie": "UMLS:C4744552", "names": ["Metastatic Pharyngeal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Pharyngeal Carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0015529", "names": ["paroxysmal hemicrania", "Paroxysmal Hemicrania", "paroxysmal Hemicrania", "Paroxysmal hemicrania", "Hemicrania, Paroxysmal", "paroxysmal; hemicrania", "hemicrania; paroxysmal", "Paroxysmal Hemicranias", "Hemicranias, Paroxysmal", "Paroxysmal hemicrania NOS", "Paroxysmal hemicrania (disorder)", "paroxysmal hemicrania (diagnosis)", "Paroxysmal hemicrania (headache one side of head)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paroxysmal Hemicrania", "shortest_name_length": 21}
{"curie": "MONDO:0021038", "names": ["EFTs", "Ewing Family of Tumors", "Ewing family of tumors", "Ewing's Family of Tumors", "tumors of Ewing's family", "Tumors of Ewing's Family", "Ewing's family of tumors", "Ewing's Family of Tumours", "Ewing's family of tumours", "Tumors of the Ewing's Family", "tumors of the Ewing's family", "Ewing sarcoma/Peripheral PNET", "Ewing sarcoma/peripheral PNET", "Ewing sarcoma family of tumors", "Ewing sarcoma/Peripheral primitive neuroectodermal tumor", "Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor", "Ewing sarcoma/peripheral primitive neuroectodermal tumor", "Ewing's sarcoma/peripheral primitive neuroectodermal tumor", "Ewing's Sarcoma/Peripheral Primitive Neuroectodermal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ewing sarcoma/peripheral primitive neuroectodermal tumor", "shortest_name_length": 4}
{"curie": "UMLS:C0278680", "names": ["Localized Parathyroid Cancer", "localized parathyroid cancer", "parathyroid cancer, localized", "localized parathyroid carcinoma", "Localized Parathyroid Carcinoma", "parathyroid carcinoma, localized", "Localized Parathyroid Gland Cancer", "cancer of the parathyroid, localized", "Localized Parathyroid Gland Carcinoma", "carcinoma of the parathyroid, localized"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized Parathyroid Gland Carcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0006352", "names": ["Accessory Sinus Adenoid Cystic Carcinoma", "accessory sinus adenoid cystic carcinoma", "paranasal sinus adenoid cystic carcinoma", "Paranasal Sinus Adenoid Cystic Carcinoma", "adenoid cystic carcinoma of paranasal sinus", "Adenoid Cystic Carcinoma of Paranasal Sinus", "adenoid cystic carcinoma of accessory sinus", "Adenoid Cystic Carcinoma of Accessory Sinus", "Adenoid Cystic Carcinoma of the Accessory Sinus", "adenoid cystic carcinoma of the paranasal sinus", "adenoid cystic carcinoma of the accessory sinus", "Adenoid Cystic Carcinoma of the Paranasal Sinus", "adenoid cystic carcinoma of accessory sinus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paranasal sinus adenoid cystic carcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0008834", "names": ["Asa triad", "ASA TRIAD", "ASA triad", "ASA Triad", "Asthma and Nasal Polyps", "ASTHMA AND NASAL POLYPS", "asthma and nasal polyps", "asthma, aspirin-induced, susceptibility to", "ASTHMA, ASPIRIN-INDUCED, SUSCEPTIBILITY TO", "Asthma, Nasal Polyps, And Aspirin Intolerance", "ASTHMA, NASAL POLYPS, AND ASPIRIN INTOLERANCE", "asthma, nasal polyps, and aspirin intolerance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "asthma, nasal polyps, and aspirin intolerance", "shortest_name_length": 9}
{"curie": "MONDO:0009792", "names": ["Clayton Smith-Donnai syndrome", "oral and digital anomalies with ichthyosis", "Oral and digital anomalies with ichthyosis", "ORAL AND DIGITAL ANOMALIES WITH ICHTHYOSIS", "ichthyosis tapered fingers midline groove up", "Ichthyosis tapered fingers midline groove up", "ichthyosis-oral and digital anomalies syndrome", "unusual facies, digital abnormalities, and ichthyosis", "Unusual facies, digital abnormalities, and ichthyosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ichthyosis-oral and digital anomalies syndrome", "shortest_name_length": 29}
{"curie": "UMLS:C4683433", "names": ["Thyroid Gland Anaplastic Carcinoma by AJCC v7 Stage", "Thyroid Gland Undifferentiated (Anaplastic) Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Anaplastic Carcinoma by AJCC v7 Stage", "shortest_name_length": 51}
{"curie": "MONDO:0013996", "names": ["FFDD2", "Type 2 FFDD", "FFDD, Type 2", "FFDD type II", "Brauer Setleis Syndrome", "BRAUER-SETLEIS SYNDROME", "Brauer-Setleis syndrome", "Brauer-Setleis Syndrome", "Focal Facial Dermal Dysplasia 2", "Bitemporal Forceps Marks Syndrome", "Focal Facial Dermal Dysplasia Type 2", "Focal facial dermal dysplasia type II", "focal facial dermal dysplasia type II", "Focal Facial Dermal Dysplasia, Type II", "Focal facial dermal dysplasia type II (disorder)", "FFDD type 2 - focal facial dermal dysplasia type 2", "Focal facial dermal dysplasia 2 Brauer Setleis type", "Focal facial dermal dysplasia 2, Brauer-Setleis type", "FOCAL FACIAL DERMAL DYSPLASIA 2, BRAUER-SETLEIS TYPE", "focal facial dermal dysplasia 2, Brauer-Setleis type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal facial dermal dysplasia type II", "shortest_name_length": 5}
{"curie": "MONDO:0013303", "names": ["AIS6", "SIAE autoimmune disease", "susceptibility to autoimmune disease 6", "AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6", "autoimmune disease, susceptibility to, 6", "autoimmune disease caused by mutation in SIAE", "autoimmune disease, susceptibility to, type 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune disease, susceptibility to, 6", "shortest_name_length": 4}
{"curie": "UMLS:C2827467", "names": ["Asbestos-Related Lung Disease", "Asbestos-Related Lung Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Asbestos-Related Lung Disorder", "shortest_name_length": 29}
{"curie": "UMLS:C5418572", "names": ["Metastatic Malignant Head and Neck Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Malignant Head and Neck Neoplasm", "shortest_name_length": 43}
{"curie": "UMLS:C4330718", "names": ["MRKH Type 2", "MURCS Syndrome", "Mullerian Duct Aplasia", "Mullerian-Renal-Cervical Spine Syndrome", "Unilateral Renal Dysplasia and Cervicothoracic Somite Anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mullerian-Renal-Cervical Spine Syndrome", "shortest_name_length": 11}
{"curie": "UMLS:C0863187", "names": ["Gastric carcinoma stage I", "Stomach carcinoma stage I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric carcinoma stage I", "shortest_name_length": 25}
{"curie": "MONDO:0017419", "names": ["AMELIA", "amelia", "Amelia", "Amelia NOS", "Amelia, NOS", "isolated amelia", "nonsyndromic amelia", "non-syndromic amelia", "Amelia of unspecified limb", "Congenital absence of limb", "absence; extremity, congenital", "Congenital absence of limb NOS", "extremity; absence, congenital", "Congenital absence of limb, NOS", "Congenital complete absence of limb", "Congenital absence of unspecified limb(s)", "Congenital complete absence of limb (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-syndromic amelia", "shortest_name_length": 6}
{"curie": "MONDO:0001427", "names": ["Dieulafoy lesion", "dieulafoy lesion", "Dieulafoy; ulcer", "ulcer; Dieulafoy", "dieulafoy lesions", "Dieulafoy disease", "dieulafoy disease", "dieulafoy's ulcer", "dieulafoy diseases", "Ulcer, Dieulafoy's", "Dieulafoy's lesion", "Calibre persistent artery", "Caliber persistent artery", "Dieulafoy lesion (diagnosis)", "Exulceratio simplex Dieulafoy", "Dieulafoy vascular malformation", "Dieulafoy's vascular malformation", "Dieulafoy lesion (hemorrhagic) of intestine", "Dieulafoy's vascular malformation (disorder)", "Dieulafoy lesion (hemorrhagic) of stomach and duodenum", "dieulafoy lesion (hemorrhagic) of stomach and duodenum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dieulafoy lesion", "shortest_name_length": 16}
{"curie": "UMLS:C4086176", "names": ["Childhood Follicular Thyroid Carcinoma", "Childhood Thyroid Gland Follicular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Thyroid Gland Follicular Carcinoma", "shortest_name_length": 38}
{"curie": "UMLS:C4525587", "names": ["Stage III Gastric Neuroendocrine Tumor", "Stage III Gastric Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Gastric Neuroendocrine Tumor AJCC v8", "shortest_name_length": 38}
{"curie": "MONDO:0019297", "names": ["lymphedema", "Lymphedema", "LYMPHEDEMA", "lymphedemas", "LYMPH EDEMA", "Lymphoedema", "Lymphedemas", "LYMPHOEDEMA", "lymphoedema", "Lymphoedemas", "Lymphedema NOS", "Lymphedema, NOS", "Lymphoedema NOS", "lymphatic edema", "Lymphatic edema", "lymphatic oedema", "Lymphatic Oedema", "Lymphoedema, NOS", "Edema, lymphatic", "Lymphatic oedema", "edema; lymphatic", "lymphatic; edema", "oedema lymphatic", "Acquired lymphedema", "Acquired lymphoedema", "Lymphedema, acquired", "LYMPHATIC OBSTRUCTION", "Lymphatic obstruction", "lymphatic obstruction", "Lymphedema (disorder)", "Lymphatic Obstruction", "lymphatics obstruction", "lymphatic; obstruction", "lymphedema (diagnosis)", "obstruction; lymphatic", "lymphatic obstruction; edema", "edema; lymphatic obstruction", "lymphedema (physical finding)", "Onset of lymphedema around puberty", "Chronic lymphovenous insufficiency", "lymphatic edema (morphologic abnormality)", "Lymphatic edema (morphologic abnormality)", "Swelling caused by excess lymph fluid under skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphedema", "shortest_name_length": 10}
{"curie": "UMLS:C4288846", "names": ["Late Prosthetic Valve Endocarditis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Late Prosthetic Valve Endocarditis", "shortest_name_length": 34}
{"curie": "MONDO:0022977", "names": ["diaphragmatic hernia exomphalos corpus callosum agenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diaphragmatic hernia exomphalos corpus callosum agenesis", "shortest_name_length": 56}
{"curie": "MONDO:0010473", "names": ["MRXS32", "mental retardation, X-linked, syndromic 32", "MENTAL RETARDATION, X-LINKED, SYNDROMIC 32", "intellectual disability, X-linked, syndromic 32", "mental retardation, X-linked, syndromic type 32", "intellectual disability, X-linked, syndromic type 32", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 32", "intellectual developmental disorder, X-linked syndromic 32, X-linked recessive", "X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C5420813", "names": ["Ectopic Lacrimal Gland in the Iris"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ectopic Lacrimal Gland in the Iris", "shortest_name_length": 34}
{"curie": "UMLS:C5237247", "names": ["Clonal Nevus", "Combined Nevus", "Inverted Type A Nevus", "Nevus with Atypical Dermal Nodules", "Nevus with Dermal Epithelioid Component", "Melanocytic Nevus with Phenotypic Heterogeneity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Combined Nevus", "shortest_name_length": 12}
{"curie": "MONDO:0023369", "names": ["maxillofacial anomaly", "maxillo-facial disease", "facial skeleton disease", "disease of facial skeleton", "disorder of facial skeleton", "facial skeleton disease or disorder", "disease or disorder of facial skeleton"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of facial skeleton", "shortest_name_length": 21}
{"curie": "MONDO:0021642", "names": ["vulvar varices", "vulval varices", "Vulval varices", "varices; vulva", "vulva; varices", "Vulval varicose vein", "Varicose veins vulval", "Varicose veins of vulva", "vulvar varices (diagnosis)", "mammalian vulva varicose disease", "Varicose veins of vulva (disorder)", "varicose disease of mammalian vulva"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulval varices", "shortest_name_length": 14}
{"curie": "UMLS:C2936233", "names": ["Postexercise Hypotension", "Hypotension, Postexercise", "Post-Exercise Hypotension", "Post Exercise Hypotension", "Postexercise Hypotensions", "Post Exercise Hypotensions", "Post-Exercise Hypotensions", "Hypotension, Post-Exercise", "Hypotension, Post Exercise", "Hypotensions, Postexercise", "Hypotensions, Post-Exercise", "Hypotensions, Post Exercise"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post-Exercise Hypotension", "shortest_name_length": 24}
{"curie": "UMLS:C1541334", "names": ["Adult Acute Myeloid Leukemia with t(9;11)(p22;q23); MLLT3-MLL", "Adult Acute Myeloid Leukemia with t(9;11)(p21;q23); MLLT3-MLL", "Adult Acute Myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3-MLL", "Acute Myeloid Leukemia (AML) with t(9;11)(p21.3;q23.3); MLLT3-KMT2A", "Adult Acute Myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3-KMT2A", "Adult Acute Myeloid Leukemia with t(9;11)(p22.3;q23.3); MLLT3-KMT2A", "Adult Acute Myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3 (AF9)-KMT2A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Acute Myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3-MLL", "shortest_name_length": 61}
{"curie": "MONDO:0013931", "names": ["PBD4B", "Peroxisome Biogenesis Disorder 4B", "peroxisome biogenesis disorder 4B", "PEROXISOME BIOGENESIS DISORDER 4B", "peroxisome biogenesis disorder type 4B", "non-classic peroxisome biogenesis disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder 4B", "shortest_name_length": 5}
{"curie": "UMLS:C4525198", "names": ["Intrahepatic Cholangiocarcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intrahepatic Cholangiocarcinoma by AJCC v7 Stage", "shortest_name_length": 48}
{"curie": "MONDO:0020165", "names": ["syndromic epicanthus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic epicanthus", "shortest_name_length": 20}
{"curie": "MONDO:0011627", "names": ["IDDAS", "AUTS5", "AUTS5, FORMERLY", "AUTISM-RELATED SPEECH DELAY", "autism-related speech delay", "autism, susceptibility to, 5", "phrase speech delay, autism-related", "PHRASE SPEECH DELAY, AUTISM-RELATED", "AUTISM, SUSCEPTIBILITY TO, 5, FORMERLY", "intellectual developmental disorder with autism and speech delay", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISM AND SPEECH DELAY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autism, susceptibility to, 5", "shortest_name_length": 5}
{"curie": "MONDO:0005073", "names": ["mole", "Mole", "nevi", "Nevi", "Nevus", "NEVUS", "Naevi", "nevus", "Moles", "NAEVUS", "Naevus", "naevus", "Skin Mole", "Skin mole", "Nevus, NOS", "Skin Moles", "Mole, Skin", "Moles, Skin", "Naevus, NOS", "mole of skin", "Mole of skin", "Skin mole, NOS", "Melanotic Nevus", "melanotic Nevus", "melanocytic Nevus", "Melanocytic nevus", "melanocytic nevus", "Melanocytic Nevus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melanocytic nevus", "shortest_name_length": 4}
{"curie": "UMLS:C0268443", "names": ["nephrogenic diabetes insipidus acquired", "acquired nephrogenic diabetes insipidus", "Acquired Nephrogenic Diabetes Insipidus", "Acquired nephrogenic diabetes insipidus", "Secondary nephrogenic diabetes insipidus", "nephrogenic diabetes insipidus, acquired", "Acquired nephrogenic diabetes insipidus (disorder)", "nephrogenic diabetes insipidus, acquired (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired Nephrogenic Diabetes Insipidus", "shortest_name_length": 39}
{"curie": "MONDO:0007907", "names": ["lipoma of the conjunctiva", "Lipoma of the Conjunctiva", "LIPOMA OF THE CONJUNCTIVA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lipoma of the conjunctiva", "shortest_name_length": 25}
{"curie": "MONDO:0014583", "names": ["CMS3A", "congenital myasthenic syndrome 3A", "congenital myasthenic syndrome type 3A", "congenital myasthenic syndrome 3A, slow-channel", "MYASTHENIC SYNDROME, CONGENITAL, 3A, SLOW-CHANNEL", "myasthenic syndrome, congenital, 3A, slow-channel"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myasthenic syndrome 3A", "shortest_name_length": 5}
{"curie": "UMLS:C0279982", "names": ["Synovial Sarcoma", "Childhood Synovial Sarcoma", "childhood synovial sarcoma", "pediatric synovial sarcoma", "Pediatric Synovial Sarcoma", "synovial sarcoma, childhood", "synovial sarcoma, pediatric", "sarcoma, synovial, childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Synovial Sarcoma", "shortest_name_length": 16}
{"curie": "MONDO:0002432", "names": ["malignant acoustic nerve tumor", "vestibulocochlear nerve cancer", "Malignant Acoustic Nerve Tumor", "Malignant Tumor of Acoustic Nerve", "malignant acoustic nerve neoplasm", "cancer of vestibulocochlear nerve", "Malignant Acoustic Nerve Neoplasm", "malignant tumor of acoustic nerve", "Cancer of Vestibulocochlear Nerve", "malignant eighth cranial nerve tumor", "malignant neoplasm of acoustic nerve", "Malignant Eighth Cranial Nerve Tumor", "Malignant neoplasm of acoustic nerve", "Malignant Neoplasm of Acoustic Nerve", "cancer of the vestibulocochlear nerve", "Malignant Tumor of the Acoustic Nerve", "malignant tumor of the acoustic nerve", "Cancer of the Vestibulocochlear Nerve", "Malignant Tumor of Eighth Cranial Nerve", "malignant tumor of eighth cranial nerve", "malignant eighth cranial nerve neoplasm", "malignant vestibulocochlear nerve tumor", "Malignant Vestibulocochlear Nerve Tumor", "Malignant Eighth Cranial Nerve Neoplasm", "Malignant Neoplasm of the Acoustic Nerve", "malignant neoplasm of the acoustic nerve", "malignant neoplasm of eighth cranial nerve", "malignant tumor of vestibulocochlear nerve", "Malignant Tumor of Vestibulocochlear Nerve", "Malignant Vestibulocochlear Nerve Neoplasm", "Malignant Neoplasm of Eighth Cranial Nerve", "malignant vestibulocochlear nerve neoplasm", "Malignant Tumor of the Eighth Cranial Nerve", "malignant tumor of the eighth cranial nerve", "malignant tumor of acoustic vestibular nerve", "Malignant tumor of acoustic vestibular nerve", "malignant tumour of acoustic vestibular nerve", "malignant neoplasm of vestibulocochlear nerve", "Malignant Neoplasm of Vestibulocochlear Nerve", "Malignant tumour of acoustic vestibular nerve", "malignant tumor of the Vestibulocochlear nerve", "Malignant Tumor of the Vestibulocochlear Nerve", "Malignant Neoplasm of the Eighth Cranial Nerve", "malignant tumor of the vestibulocochlear nerve", "malignant neoplasm of the eighth cranial nerve", "malignant neoplasm of the vestibulocochlear nerve", "Malignant Neoplasm of the Vestibulocochlear Nerve", "malignant neoplasm of acoustic vestibular nerve (VIII)", "malignant neoplasm of eighth cranial nerve (diagnosis)", "Malignant tumor of acoustic vestibular nerve (disorder)", "malignant neoplasm of acoustic vestibular nerve (VIII) (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant neoplasm of acoustic nerve", "shortest_name_length": 30}
{"curie": "MONDO:0017988", "names": ["MAT", "Ectopic atrial tachycardia", "chaotic atrial tachycardia", "Chaotic atrial tachycardia", "multifocal atrial tachycardia", "Multifocal atrial tachycardia", "MULTIFOCAL ATRIAL TACHYCARDIA", "Multifocal Atrial Tachycardia", "ATRIAL TACHYCARDIA MULTIFOCAL", "multifocal atrial tachycardia (disease)", "Multifocal atrial tachycardia (disorder)", "multifocal atrial tachycardia (diagnosis)", "Multifocal Atrial Tachycardia by EKG Finding", "Multifocal Atrial Tachycardia by ECG Finding"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multifocal atrial tachycardia", "shortest_name_length": 3}
{"curie": "MONDO:0012928", "names": ["SPG42", "hereditary spastic paraplegia 42", "hereditary spastic paraplegia type 42", "autosomal dominant spastic paraplegia 42", "spastic paraplegia 42, autosomal dominant", "SPASTIC PARAPLEGIA 42, AUTOSOMAL DOMINANT", "Spastic Paraplegia 42, Autosomal Dominant", "Autosomal dominant spastic paraplegia type 42", "autosomal dominant spastic paraplegia type 42", "SLC33A1 autosomal dominant pure spastic paraplegia", "familial spastic paraplegia autosomal dominant type 42", "Autosomal dominant spastic paraplegia type 42 (disorder)", "Autosomal dominant spastic paraplegia type 42 (diagnosis)", "autosomal dominant pure spastic paraplegia caused by mutation in SLC33A1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 42", "shortest_name_length": 5}
{"curie": "UMLS:C4726549", "names": ["Myeloid Neoplasms with Germline ANKRD26 Mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myeloid Neoplasms with Germline ANKRD26 Mutation", "shortest_name_length": 48}
{"curie": "UMLS:C0409679", "names": ["seronegative arthritis", "Seronegative arthritis", "arthritis seronegative", "seronegative arthropathy", "Seronegative arthropathy", "Sero negative arthropathy", "sero negative arthropathy", "seronegative polyarthritis", "Seronegative arthritis NOS", "Seronegative polyarthritis", "Seronegative arthritis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Seronegative arthritis", "shortest_name_length": 22}
{"curie": "MONDO:0012710", "names": ["HSCR9", "Hirschsprung disease, susceptibility to, 9", "HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hirschsprung disease, susceptibility to, 9", "shortest_name_length": 5}
{"curie": "MONDO:0021084", "names": ["DISORDER SIGHT", "disorders sight", "visual disorder", "Visual Disorder", "Vision Disorder", "Vision disorder", "Visual disorder", "vision disorder", "disorders vision", "vision disorders", "visual; disorder", "Vision disorders", "Vision Disorders", "disorder; visual", "disorders visual", "Visual Disorders", "VISION DISORDERS", "Disorder, Visual", "Disorders, Visual", "disorders visions", "Disorder of vision", "Visual dysfunction", "disorder of vision", "vision dysfunction", "Dysfunction;vision", "visual dysfunction", "Vision disorder, NOS", "Visual Field Disorder", "visual Field disorder", "Visual system disorder", "visual system disorder", "Visual System Disorder", "Disorder of vision, NOS", "Disorder of Visual System", "disorder of visual system", "vision disorder (diagnosis)", "Disorder of vision (disorder)", "Visual system disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vision disorder", "shortest_name_length": 14}
{"curie": "UMLS:C4527185", "names": ["Stage IIIA", "Stage IIIA Cutaneous (Skin) Melanoma", "Pathologic Stage IIIA Cutaneous Melanoma AJCC v8", "Pathologic Stage IIIA Melanoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IIIA Cutaneous Melanoma AJCC v8", "shortest_name_length": 10}
{"curie": "MONDO:0004227", "names": ["epididymal adenomatoid tumor", "epididymis adenomatoid tumor", "Epididymal Adenomatoid Tumor", "Adenomatoid Tumor of Epididymis", "Adenomatoid tumor of epididymis", "adenomatoid tumor of epididymis", "Adenomatoid tumour of epididymis", "Adenomatoid Neoplasm of Epididymis", "adenomatoid neoplasm of epididymis", "adenomatoid tumor of the epididymis", "Adenomatoid Tumor of the Epididymis", "adenomatoid neoplasm of the epididymis", "Adenomatoid Neoplasm of the Epididymis", "benign Epididymal epithelial Mesothelioma", "benign epididymal epithelial mesothelioma", "Benign Epididymal Epithelial Mesothelioma", "Adenomatoid tumor of epididymis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epididymal adenomatoid tumor", "shortest_name_length": 28}
{"curie": "UMLS:C4528625", "names": ["Stage IVB Vulvar Cancer", "Stage IVB Vulvar Cancer AJCC v8", "Stage IVB Vulvar Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Vulvar Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "MONDO:0010996", "names": ["HHT3", "ORW3", "Osler-rendu-weber syndrome 3", "Osler Weber Rendu syndrome type 3", "telangiectasia hereditary hemorrhagic type 3", "hereditary hemorrhagic telangiectasia type 3", "TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 3", "Telangiectasia, hereditary hemorrhagic, type 3", "telangiectasia, hereditary hemorrhagic, type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary hemorrhagic telangiectasia type 3", "shortest_name_length": 4}
{"curie": "MONDO:0007197", "names": ["Bladder diverticula", "bladder diverticulum", "diverticulum bladder", "Bladder diverticulum", "Bladder Diverticulum", "BLADDER DIVERTICULUM", "BLADDER, DIVERTICULUM", "bladder; diverticulum", "diverticulum; bladder", "diverticulum - bladder", "Diverticulum - bladder", "of bladder diverticulum", "diverticulum of bladder", "Diverticulum of bladder", "bladder diverticulum (disease)", "Diverticulum of bladder (disorder)", "diverticulum of bladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder diverticulum", "shortest_name_length": 19}
{"curie": "MONDO:0001265", "names": ["SCHIZOPHRENIFORM ILLNESS", "Schizophreniform illness", "Schizophreniform disorder", "SCHIZOPHRENIFORM DISORDER", "Schizophreniform Disorder", "schizophreniform disorder", "disorder; schizophreniform", "Disorder, Schizophreniform", "schizophreniform; disorder", "Schizophreniform Disorders", "Disorders, Schizophreniform", "Schizophreniform disorder, NOS", "Schizophreniform disorder (disorder)", "schizophreniform disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schizophreniform disorder", "shortest_name_length": 24}
{"curie": "MONDO:0002306", "names": ["Angular blepharoconjunctivitis", "angular blepharoconjunctivitis", "Angular blepharoconjunctivitis, NOS", "Angular blepharoconjunctivitis (disorder)", "angular blepharoconjunctivitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angular blepharoconjunctivitis", "shortest_name_length": 30}
{"curie": "MONDO:0011540", "names": ["SCA14", "spinocerebellar ataxia 14", "Spinocerebellar ataxia 14", "SPINOCEREBELLAR ATAXIA 14", "Spinocerebellar ataxia type 14", "spinocerebellar ataxia type 14", "SCA14 Spinocerebellar ataxia 14", "Spinocerebellar ataxia type 14 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia type 14", "shortest_name_length": 5}
{"curie": "MONDO:0011512", "names": ["SBS", "Bss", "BSS", "BRSS", "CYLD cutaneous syndrome", "SPIEGLER-BROOKE SYNDROME", "Spiegler-Brooke Syndrome", "BROOKE-SPIEGLER SYNDROME", "Brooke-Spiegler syndrome", "Spiegler-Brooke syndrome", "Brooke-Spiegler syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brooke-Spiegler syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0015746", "names": ["globozoospermia", "globozoospermia syndrome", "round-headed sperm syndrome", "male infertility due to globozoospermia", "Male infertility due to round-headed spermatozoa", "male infertility due to round-headed spermatozoa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "male infertility due to globozoospermia", "shortest_name_length": 15}
{"curie": "MONDO:0012340", "names": ["CELIAC2", "celiac disease, susceptibility to, 2", "CELIAC DISEASE, SUSCEPTIBILITY TO, 2", "gluten-sensitive enteropathy, susceptibility to, 2", "GLUTEN-SENSITIVE ENTEROPATHY, SUSCEPTIBILITY TO, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "celiac disease, susceptibility to, 2", "shortest_name_length": 7}
{"curie": "MONDO:0017188", "names": ["diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency", "hyperinsulinemic hypoglycemia due to Kir6.2 deficiency, diazoxide-resistant focal form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency", "shortest_name_length": 66}
{"curie": "UMLS:C4726622", "names": ["Refractory Fallopian Tube Cancer", "Refractory Fallopian Tube Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Fallopian Tube Carcinoma", "shortest_name_length": 32}
{"curie": "EFO:0009854", "names": ["treatment resistant depression"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "treatment resistant depression", "shortest_name_length": 30}
{"curie": "MONDO:0012301", "names": ["MTDPS2", "mitochondrial DNA depletion syndrome 2", "mtDNA depletion syndrome, myopathic form", "mitochondrial DNA depletion syndrome type 2", "TK2-related mitochondrial DNA depletion myopathy", "mitochondrial DNA depletion myopathy, Tk2-related", "MITOCHONDRIAL DNA DEPLETION MYOPATHY, TK2-RELATED", "Mitochondrial DNA Depletion Syndrome, Myopathic Form", "Mitochondrial DNA depletion syndrome, myopathic form", "mitochondrial DNA depletion syndrome, myopathic form", "Mitochondrial DNA depletion syndrome 2 myopathic type", "MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)", "Mitochondrial DNA Depletion Syndrome 2 (Myopathic Type)", "mitochondrial DNA depletion syndrome 2 (myopathic type)", "Mitochondrial DNA Depletion Myopathy, Autosomal Recessive", "TK2-related mitochondrial DNA depletion syndrome myopathic form", "TK2-related mitochondrial DNA depletion syndrome, myopathic form", "TK2-related mitochondrial deoxyribonucleic acid depletion syndrome myopathic form", "TK2-related mitochondrial deoxyribonucleic acid depletion syndrome myopathic form (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial DNA depletion syndrome, myopathic form", "shortest_name_length": 6}
{"curie": "MONDO:0017176", "names": ["SCA3, Machado type", "azorean disease, type iii", "Azorean disease, type III", "Machado-Joseph disease type 3", "Azorean disease, type III (disorder)", "spinocerebellar ataxia type 3, Machado type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Machado-Joseph disease type 3", "shortest_name_length": 18}
{"curie": "MONDO:0018334", "names": ["Chronic hiccup", "hiccup chronic", "HICCUP CHRONIC", "chronic hiccup", "Chronic hiccups", "chronic hiccups", "Chronic hiccough", "Chronic hiccoughs", "persistent hiccups", "intractable hiccups", "Hiccups, intractable", "intractable singultus", "Chronic hiccup (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic hiccup", "shortest_name_length": 14}
{"curie": "MONDO:0010536", "names": ["tubulin, beta", "TUBULIN, BETA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tubulin, beta", "shortest_name_length": 13}
{"curie": "MONDO:0014830", "names": ["BDPLT20", "platelet-type bleeding disorder 20", "BLEEDING DISORDER, PLATELET-TYPE, 20", "bleeding disorder, platelet-type, 20", "SLFN14 inherited bleeding disorder, platelet-type", "autosomal dominant thrombocytopenia with platelet secretion defect", "inherited bleeding disorder, platelet-type caused by mutation in SLFN14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "platelet-type bleeding disorder 20", "shortest_name_length": 7}
{"curie": "MONDO:0015701", "names": ["IL-7R", "IL-7Ralpha deficiency", "T-B+ SCID due to IL-7Ralpha deficiency", "interleukin-7 receptor alpha deficiency", "T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0020575", "names": ["Multiform ventricular tachycardia", "Multifocal ventricular tachycardia", "Polymorphic Ventricular Tachycardia", "polymorphic ventricular tachycardia", "Polymorphic ventricular tachycardia", "ventricular tachycardia, polymorphic", "Ventricular tachycardia, polymorphic", "Ventricular tachycardia, polymorphic (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polymorphic ventricular tachycardia", "shortest_name_length": 33}
{"curie": "MONDO:0015696", "names": ["Good syndrome", "GOOD SYNDROME", "good syndrome", "goods syndrome", "Good's syndrome", "thymus Good syndrome", "thymoma-immunodeficiency", "Good syndrome (diagnosis)", "THYMOMA WITH IMMUNODEFICIENCY", "Immunodeficiency with thymoma", "immunodeficiency with thymoma", "Thymoma-immunodeficiency syndrome", "thymoma-immunodeficiency syndrome", "thymoma with hypogammaglobulinemia", "Immunodeficiency with thymoma (disorder)", "immunodeficiency with thymoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Good syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0019398", "names": ["early-onset desmin-related myopathy", "desmin-related myopathy with Mallory body-like inclusions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "desmin-related myopathy with Mallory body-like inclusions", "shortest_name_length": 35}
{"curie": "UMLS:C1142249", "names": ["infected cyst", "Infected cyst", "cyst infected", "cysts infected"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infected cyst", "shortest_name_length": 13}
{"curie": "MONDO:0014972", "names": ["chromosome 19q13.11 deletion syndrome, proximal", "CHROMOSOME 19q13.11 DELETION SYNDROME, PROXIMAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 19q13.11 deletion syndrome, proximal", "shortest_name_length": 47}
{"curie": "UMLS:C0855037", "names": ["Localized Alveolar Soft Part Sarcoma", "Alveolar Soft Part Sarcoma Nonmetastatic", "Alveolar soft part sarcoma non-metastatic", "Non-Metastatic Alveolar Soft Part Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alveolar soft part sarcoma non-metastatic", "shortest_name_length": 36}
{"curie": "MONDO:0004525", "names": ["Scabies", "SCABIES", "scabies", "Sarcoptic itch", "SARCOPTIC ITCH", "sarcoptic itch", "scabies (diagnosis)", "Scabies infestation", "scabies; infestation", "infestation; scabies", "Scabies <infestation>", "infestation; mites, scabic", "mites; infestation, scabic", "acariasis; Sarcoptes scabiei", "Sarcoptes scabiei; acariasis", "Sarcoptes scabeii infestation", "infestation; Sarcoptes scabiei", "Sarcoptes scabiei; infestation", "infestation by Sarcoptes scabiei", "Infestation by Sarcoptes scabiei", "Sarcoptes scabiei infectious disease", "Sarcoptes scabiei disease or disorder", "Sarcoptes scabiei caused disease or disorder", "Infestation by Sarcoptes scabiei var hominis", "infestation by Sarcoptes scabiei var hominis", "Infestation caused by Sarcoptes scabiei var hominis", "Infestation caused by Sarcoptes scabiei var hominis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scabies", "shortest_name_length": 7}
{"curie": "MONDO:0019260", "names": ["Kufs", "ANCL", "Adult NCL", "adult NCL", "Kuf Disease", "kuf disease", "Kufs disease", "kufs disease", "Kufs Disease", "kuf's disease", "Kuf's disease", "Kufs' disease", "Kuf's Disease", "kufs' disease", "Disease, Kufs'", "Disease, Kuf's", "ceroid lipofuscinosis", "Kufs disease (diagnosis)", "Amaurotic idiocy adult type", "Adult-type amaurotic idiocy", "Amaurotic Idiocy, Adult Type", "Late familial amaurotic idiocy", "Neuronal lipofuscinosis, adult", "Amaurotic idiocy late familial", "neuronal ceroid lipofuscinosis 4", "Ceroid Lipofuscinosis, Neuronal 4", "adult neuronal ceroid lipofuscinosis", "Adult Neuronal Ceroid Lipofuscinosis", "Adult neuronal ceroid lipofuscinosis", "Kufs disease (ceroid lipofuscinosis)", "Neuronal Ceroid Lipofuscinosis, Adult", "CLN4 disease, adult autosomal dominant", "Kufs type neuronal ceroid lipofuscinosis", "neuronal ceroid lipofuscinosis of adults", "Kufs Type Neuronal Ceroid Lipofuscinosis", "Neuronal Ceroid Lipofuscinosis, Adult Type", "Adult neuronal ceroid lipofuscinosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult neuronal ceroid lipofuscinosis", "shortest_name_length": 4}
{"curie": "UMLS:C1265832", "names": ["Focal acute inflammation", "Focal Acute Inflammation", "Localised acute inflammation", "Localized acute inflammation", "Circumscribed acute inflammation", "Focal acute inflammation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Focal acute inflammation", "shortest_name_length": 24}
{"curie": "MONDO:0030524", "names": ["MPS10", "ARSK DEFICIENCY", "ARYLSULFATASE K DEFICIENCY", "MUCOPOLYSACCHARIDOSIS, TYPE X", "mucopolysaccharidosis, type 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucopolysaccharidosis, type 10", "shortest_name_length": 5}
{"curie": "UMLS:C4683610", "names": ["Lugano Classification Stage IIE Adult Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage IIE Adult Hodgkin Lymphoma AJCC v8", "shortest_name_length": 62}
{"curie": "UMLS:C2981269", "names": ["Stage III Differentiated Thyroid Gland Cancer", "Stage III Differentiated Thyroid Gland Carcinoma", "Stage III Differentiated Thyroid Gland Carcinoma AJCC v7", "Stage III Thyroid Gland Papillary or Follicular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Differentiated Thyroid Gland Carcinoma AJCC v7", "shortest_name_length": 45}
{"curie": "MONDO:0014810", "names": ["CVID13", "Cid due to IKAROS deficiency", "common variable immunodeficiency 13", "pancytopenia due to IKZF1 mutations", "IMMUNODEFICIENCY, COMMON VARIABLE, 13", "immunodeficiency, common variable, 13", "immunodeficiency, common variable, type 13", "IKZF1 syndrome with combined immunodeficiency", "combined immunodeficiency due to IKAROS deficiency", "syndrome with combined immunodeficiency caused by mutation in IKZF1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancytopenia due to IKZF1 mutations", "shortest_name_length": 6}
{"curie": "MONDO:0032940", "names": ["RP88", "RETINITIS PIGMENTOSA 88", "retinitis pigmentosa 88"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 88", "shortest_name_length": 4}
{"curie": "UMLS:C5447328", "names": ["SCID-RAG1", "RAG1 Deficiency", "Severe Combined Immunodeficiency due to RAG1 Deficiency", "Severe Combined Immunodeficiency, T cell-Negative, B cell-Negative, RAG1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Severe Combined Immunodeficiency due to RAG1 Deficiency", "shortest_name_length": 9}
{"curie": "MONDO:0011881", "names": ["SPPK3", "KPPS3", "PPKS3", "Striate palmoplantar keratoderma 3", "Keratosis palmoplantaris striata 3", "keratosis palmoplantaris striata 3", "striate palmoplantar keratoderma 3", "keratosis palmoplantaris striata III", "Keratosis Palmoplantaris Striata III", "Striate Palmoplantar Keratoderma III", "KERATOSIS PALMOPLANTARIS STRIATA III", "STRIATE PALMOPLANTAR KERATODERMA III", "KRT1 striate palmoplantar keratoderma", "keratosis palmoplantaris striata type 3", "keratoderma palmoplantar striate form 3", "Keratoderma palmoplantar striate form 3", "keratoderma, palmoplantar, striate form 3", "Keratoderma, Palmoplantar, Striate Form III", "KERATODERMA, PALMOPLANTAR, STRIATE FORM III", "striate palmoplantar keratoderma caused by mutation in KRT1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratosis palmoplantaris striata 3", "shortest_name_length": 5}
{"curie": "MONDO:0003038", "names": ["dysgraphia", "Dysgraphia", "dysgraphia (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dysgraphia", "shortest_name_length": 10}
{"curie": "MONDO:0017057", "names": ["hereditary thrombocytopenia with normal platelets"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary thrombocytopenia with normal platelets", "shortest_name_length": 49}
{"curie": "MONDO:0006076", "names": ["adrenal neuroblastoma", "Adrenal neuroblastoma", "Adrenal Neuroblastoma", "neuroblastoma of adrenal", "Neuroblastoma of Adrenal", "Adrenal Gland Neuroblastoma", "adrenal gland neuroblastoma", "neuroblastoma of the adrenal", "Neuroblastoma of the Adrenal", "Neuroblastoma of Adrenal Gland", "neuroblastoma of adrenal gland", "neuroblastoma of Adrenal gland", "Adrenal neuroblastoma (disorder)", "Adrenal neuroblastoma (diagnosis)", "neuroblastoma of the adrenal gland", "Neuroblastoma of the Adrenal Gland", "malignant neoplasm neuroblastoma adrenal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adrenal gland neuroblastoma", "shortest_name_length": 21}
{"curie": "MONDO:0014875", "names": ["FH 4", "HALD4", "FH IV", "hyperaldosteronism, familial, type 4", "HYPERALDOSTERONISM, FAMILIAL, TYPE IV", "hyperaldosteronism, familial, type IV", "ALDOSTERONISM, PRIMARY, AND HYPERTENSION", "aldosteronism, primary, and hypertension", "hyperaldosteronism, familial, type IV; HALD4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperaldosteronism, familial, type IV", "shortest_name_length": 4}
{"curie": "UMLS:C2609310", "names": ["Aseptic endophthalmitis", "Non-infectious endophthalmitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-infectious endophthalmitis", "shortest_name_length": 23}
{"curie": "MONDO:0005953", "names": ["Fibrocarcinoma", "fibrocarcinoma", "Scirrhous carcinoma", "scirrhous carcinoma", "Scirrhous Carcinoma", "Carcinoma, Scirrhous", "Scirrhous Carcinomas", "Carcinomas, Scirrhous", "Scirrhous Adenocarcinoma", "Scirrhous adenocarcinoma", "scirrhous adenocarcinoma", "adenocarcinoma scirrhous", "Scirrhous Adenocarcinomas", "Adenocarcinoma, Scirrhous", "Adenocarcinomas, Scirrhous", "FIBROADENOCARCINOMA, malignant", "FIBROADENOCARCINOMA, MALIGNANT", "Carcinoma with productive fibrosis", "scirrhous adenocarcinoma (diagnosis)", "adenocarcinoma with productive fibrosis", "Adenocarcinoma With Productive Fibrosis", "Adenocarcinoma with Productive Fibrosis", "adenocarcinoma with Productive Fibrosis", "malignant neoplasm adenocarcinoma scirrhous", "scirrhous adenocarcinoma (morphologic abnormality)", "Scirrhous adenocarcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scirrhous adenocarcinoma", "shortest_name_length": 14}
{"curie": "UMLS:C5419464", "names": ["Acute Myeloid Leukemia Arising from Previous Myeloproliferative Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Myeloid Leukemia Arising from Previous Myeloproliferative Neoplasm", "shortest_name_length": 72}
{"curie": "UMLS:C4330904", "names": ["Osteoclast-Rich Osteopetrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Osteoclast-Rich Osteopetrosis", "shortest_name_length": 29}
{"curie": "MONDO:0014889", "names": ["SNDC", "Lenk-Ploski syndrome", "LENK-PLOSKI SYNDROME", "Lenk Ploski syndrome", "STRIATONIGRAL DEGENERATION, CHILDHOOD-ONSET", "striatonigral Degeneration, childhood-onset", "striatonigral degeneration, childhood-onset", "striatonigral degeneration, childhood-onset; SNDC", "childhood-onset basal ganglia degeneration syndrome", "Childhood-onset basal ganglia degeneration syndrome", "Childhood-onset basal ganglia degeneration syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "striatonigral degeneration, childhood-onset", "shortest_name_length": 4}
{"curie": "MONDO:0700109", "names": ["skin disease caused by bacterial infection, non-human animal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin disease caused by bacterial infection, non-human animal", "shortest_name_length": 60}
{"curie": "UMLS:C0242656", "names": ["Progression", "course illness", "Disease Course", "disease course", "courses disease", "Disorder Course", "course of illness", "Course of Illness", "Course of illness", "Course of disorder", "Disease Progression", "Disease progression", "disease progression", "Progression, Disease", "Disease progression NOS", "Course of illness (attribute)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disease Progression", "shortest_name_length": 11}
{"curie": "MONDO:0006597", "names": ["Sun sensitivity", "Photodermatitis", "sun sensitivity", "SUN SENSITIVITY", "photodermatosis", "photodermatitis", "Photosensitivity", "PHOTOSENSITIVITY", "photosensitivity", "Photodermatitides", "photodermatitides", "photosensitization", "Photosensitization", "Photosensitive skin", "Photodermatitis, NOS", "Skin photosensitivity", "Skin Photosensitivity", "skin photosensitivity", "PHOTOSENSITIVITY (NOS)", "Sensitivity to sunlight", "photosensitivity disease", "Photosensitivity of skin", "Photosensitivity Disorder", "photosensitivity disorder", "Photosensitive skin rashes", "Photosensitivity Disorders", "Photosensitivity disorders", "Photodermatitis (disorder)", "Disorder, Photosensitivity", "Photosensitivity (finding)", "disorder, photosensitivity", "Cutaneous photosensitivity", "photosensitivity dermatitis", "Photosensitivity dermatitis", "disorders, photosensitivity", "photodermatitis (diagnosis)", "Disorders, Photosensitivity", "Photosensitiveness due to sun", "abnormal skin photosensitivity", "abnormal skin sensitivity to sunlight", "abnormal skin sensitivity to sunlight (symptom)", "abnormal skin sensitivity to sunlight (photosensitivity)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "photosensitivity disease", "shortest_name_length": 15}
{"curie": "UMLS:C0431357", "names": ["External hydrocephalus", "External Hydrocephalus", "external hydrocephalus", "Hydrocephalus, external", "External hydrocephalus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "External hydrocephalus", "shortest_name_length": 22}
{"curie": "MONDO:0005096", "names": ["SCC", "CARCINOMA SQUAMOUS", "Carcinoma squamous", "Squamous carcinoma", "squamous carcinoma", "Squamous Carcinoma", "Carcinoma, Squamous", "squamous carcinomas", "Squamous Carcinomas", "Carcinomas, Squamous", "squamous cell cancer", "Epidermoid Carcinoma", "epidermoid carcinoma", "Carcinoma epidermoid", "Squamous cell cancer", "Epidermoid carcinoma", "Squamous Cell Cancer", "cancer cell squamous", "CARCINOMA EPIDERMOID", "cancer squamous cell", "Epidermoid Carcinomas", "cancer cells squamous", "Cell Cancer, Squamous", "squamous cell cancers", "Carcinoma, Epidermoid", "Cancer, Squamous Cell", "Squamous Cell Cancers", "Cancers, Squamous Cell", "Cell Cancers, Squamous", "epidermoid cell cancer", "Carcinomas, Epidermoid", "Epidermoid Cell Cancer", "Planocellular carcinoma", "SQUAMOUS CELL CARCINOMA", "squamous cell carcinoma", "Squamous Cell Carcinoma", "Squamous cell carcinoma", "Planocellular Carcinoma", "Malignant squamous tumor", "Squamous Cell Carcinomas", "Carcinoma, Squamous Cell", "squamous cell carcinomas", "Planocellular Carcinomas", "Carcinoma, Planocellular", "squamous cell Epithelioma", "Squamous Cell Epithelioma", "Carcinomas, Planocellular", "Carcinomas, Squamous Cell", "squamous cell epithelioma", "Epidermoid carcinoma, NOS", "Malignant squamous tumour", "Squamous cell epithelioma", "Squamous cell carcinoma NOS", "Squamous cell carcinoma, NOS", "Squamous Cell Carcinoma, NOS", "SCC - squamous cell carcinoma", "Malignant Squamous Cell Tumor", "malignant squamous cell tumor", "SCC - Squamous cell carcinoma", "malignant epidermoid cell tumor", "Malignant Epidermoid Cell Tumor", "Malignant Squamous Cell Neoplasm", "malignant squamous cell neoplasm", "Malignant squamous cell neoplasm", "Squamous cell carcinoma (disorder)", "Malignant Epidermoid Cell Neoplasm", "malignant epidermoid cell neoplasm", "CARCINOMA, SQUAMOUS CELL, MALIGNANT", "squamous cell carcinoma (diagnosis)", "carcinoma, squamous cell, malignant", "Squamous Cell Carcinoma, conventional", "Squamous Cell Carcinoma, Not Otherwise Specified", "squamous cell carcinoma (morphologic abnormality)", "Squamous cell carcinoma (morphologic abnormality)", "squamous cell carcinoma NOS (morphologic abnormality)", "Malignant squamous cell neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "squamous cell carcinoma", "shortest_name_length": 3}
{"curie": "UMLS:C0149722", "names": ["LMM In Situ", "Lentigo maligna", "lentigo maligna", "LENTIGO MALIGNA", "Lentigo Maligna", "Melanotic Freckle", "Malignant Lentigo", "lentigo malignant", "melanotic freckle", "Lentigo, Malignant", "Melanotic Freckles", "Freckle, Melanotic", "Malignant Lentigos", "Freckles, Melanotic", "Lentigos, Malignant", "LM - Lentigo maligna", "Lentigo maligna (disorder)", "lentigo maligna (diagnosis)", "Hutchinson Melanotic Freckle", "Hutchinson melanotic freckle", "Hutchinsons Melanotic Freckle", "Hutchinsons melanotic freckle", "hutchinson's melanotic freckle", "Hutchinson's Melanotic Freckle", "Hutchinson's melanotic freckle", "Melanotic Freckle, Hutchinson's", "Freckle, Hutchinson's Melanotic", "Melanotic freckle of Hutchinson", "Lentigo Maligna Melanoma In Situ", "Hutchinson melanotic freckle, NOS", "Hutchinson's melanotic freckle NOS", "Hutchinson's melanotic freckle, NOS", "Lentigo maligna (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hutchinson's Melanotic Freckle", "shortest_name_length": 11}
{"curie": "MONDO:0015761", "names": ["10p trisomy", "Trisomy 10p", "trisomy 10p", "10p+ syndrome", "10p duplication", "Duplication 10p", "trisomy type 10p", "dup(10p) syndrome", "partial trisomy 10p", "Trisomy 10p (disorder)", "chromosome 10p trisomy", "Trisomy 10p (diagnosis)", "10p duplication syndrome", "duplication 10p syndrome", "Chromosome 10, trisomy 10p", "chromosome 10p duplication", "chromosome 10p duplication syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trisomy 10p", "shortest_name_length": 11}
{"curie": "MONDO:0007428", "names": ["deafness-craniofacial syndrome", "deafness craniofacial syndrome", "Deafness-Craniofacial Syndrome", "Deafness-craniofacial syndrome", "Deafness craniofacial syndrome", "DEAFNESS-CRANIOFACIAL SYNDROME", "Hearing loss-craniofacial syndrome", "Deafness craniofacial syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness-craniofacial syndrome", "shortest_name_length": 30}
{"curie": "UMLS:C0156229", "names": ["Nephrotic syndrome with lesion of lobular glomerulonephritis", "Nephrotic Syndrome with Lesion of Lobular Glomerulonephritis", "Nephrotic syndrome with lesion of mesangiocapillary glomerulonephritis", "Nephrotic Syndrome with Lesion of Mesangiocapillary Glomerulonephritis", "Nephrotic Syndrome with Lesion of Membranoproliferative Glomerulonephritis", "Nephrotic syndrome with lesion of membranoproliferative glomerulonephritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic syndrome with lesion of membranoproliferative glomerulonephritis", "shortest_name_length": 60}
{"curie": "MONDO:0015437", "names": ["R21", "Ring 21", "ring chromosome 21", "chromosome 21 ring", "Chromosome 21 ring", "Ring 21, Chromosome", "Ring chromosome type 21", "chromosome 21 en anneau", "Ring Chromosome 21 Syndrome", "Ring chromosome 21 syndrome", "Ring chromosome 21 syndrome (disorder)", "Ring chromosome 21 syndrome (diagnosis)", "anomaly of chromosome pair ring 21 syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ring chromosome 21", "shortest_name_length": 3}
{"curie": "MONDO:0042913", "names": ["Schrander-Stumpel Theunissen Hulsmans syndrome", "Schrander-stumpel-Theunissen-Hulsmans syndrome", "vitiligo, psychomotor retardation, cleft palate and facial dysmorphism", "Vitiligo, psychomotor retardation, cleft palate and facial dysmorphism", "vitiligo vulgaris, cleft palate, somatic and psychomotor retardation and facial dysmorphism", "Vitiligo vulgaris, cleft palate, somatic and psychomotor retardation and facial dysmorphism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Schrander-stumpel-Theunissen-Hulsmans syndrome", "shortest_name_length": 46}
{"curie": "UMLS:C4688275", "names": ["Recurrent Lymphoproliferative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Lymphoproliferative Disorder", "shortest_name_length": 38}
{"curie": "MONDO:0018780", "names": ["congenital generalized hypercontractile muscle stiffness syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital generalized hypercontractile muscle stiffness syndrome", "shortest_name_length": 65}
{"curie": "UMLS:C0919914", "names": ["postoperative abscess", "Postoperative abscess", "postoperative; abscess", "postoperative abscess (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postoperative abscess", "shortest_name_length": 21}
{"curie": "MONDO:0008763", "names": ["ALMS", "ALSS", "ALSTROM SYNDROME", "Alström syndrome", "Alstrom syndrome", "Alström Syndrome", "alstrom syndrome", "Alstrom Syndrome", "Alstroms Syndrome", "Syndrome, Alström", "Alstroem syndrome", "Syndrome, Alstrom", "alstroms syndrome", "Alstrom's syndrome", "alstrom's syndrome", "Alstrom's Syndrome", "Syndrome, Alstrom's", "Alstrom-Hallgren Syndrome", "Alstrom Hallgren Syndrome", "Syndrome, Alstrom-Hallgren", "Alstrom syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alstrom syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C3641221", "names": ["Papillary Carcinoma of the Penis, NOS", "Papillary Carcinoma of the Penis, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Papillary Carcinoma of the Penis, Not Otherwise Specified", "shortest_name_length": 37}
{"curie": "MONDO:0011392", "names": ["DFNB20", "autosomal recessive deafness 20", "Deafness, Autosomal Recessive 20", "DEAFNESS, AUTOSOMAL RECESSIVE 20", "deafness, autosomal recessive 20", "autosomal recessive nonsyndromic deafness 20", "autosomal recessive nonsyndromic hearing loss 20", "autosomal recessive nonsyndromic deafness type 20"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 20", "shortest_name_length": 6}
{"curie": "MONDO:0014515", "names": ["CCMD", "MACULAR DYSTROPHY WITH CENTRAL CONE INVOLVEMENT", "macular dystrophy with central cone involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macular dystrophy with central cone involvement", "shortest_name_length": 4}
{"curie": "UMLS:C0272677", "names": ["metacarpal fracture", "Metacarpal fracture", "METACARPAL FRACTURE", "metacarpus fracture", "fracture; metacarpal", "Metacarpal fractures", "fractured metacarpal", "fractures metacarpal", "metacarpal; fracture", "Fractured metacarpal", "Fracture;metacarpal(s)", "Fracture of metacarpus", "bone fractures metacarpal", "fracture; hand, metacarpal", "hand; fracture, metacarpal", "fracture of metacarpal bone", "Fracture of metacarpus, NOS", "Fracture of metacarpal bone", "Fracture of Metacarpal Bone", "Fracture of metacarpal bones", "Fracture of metacarpal bone(s)", "Hand fracture - metacarpal bone", "fracture of the metacarpal bones", "Fracture of metacarpal bone, NOS", "Fracture of metacarpal bone (disorder)", "fracture of metacarpal bone (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fracture of metacarpal bone", "shortest_name_length": 19}
{"curie": "MONDO:0013551", "names": ["SPG47", "CPSQ5", "CPSQ5, FORMERLY", "Spastic Paraplegia 47", "hereditary spastic paraplegia 47", "AP4B1 hereditary spastic paraplegia", "hereditary spastic paraplegia type 47", "spastic quadriplegic cerebral palsy 5", "cerebral palsy, spastic quadriplegic, 5", "autosomal recessive spastic paraplegia 47", "SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE", "spastic paraplegia 47, autosomal recessive", "cerebral palsy, spastic quadriplegic, 5, formerly", "CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 5, FORMERLY", "hereditary spastic paraplegia caused by mutation in AP4B1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 47", "shortest_name_length": 5}
{"curie": "MONDO:0007188", "names": ["Bull-Nixon syndrome", "primary basilar impression", "Basilar Impression, Primary", "BASILAR IMPRESSION, PRIMARY", "basilar impression, primary", "primary basilar invagination"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary basilar invagination", "shortest_name_length": 19}
{"curie": "MONDO:0001416", "names": ["Gynecologic Cancer", "gynecologic cancer", "cancer gynecologic", "GYNECOLOGIC CANCER", "cancers gynecologic", "Genital neoplasm, female", "Female Reproductive Cancer", "female reproductive cancer", "malignant Gynecologic tumor", "cancers female reproductive", "malignant gynecologic tumor", "Malignant Gynecologic Tumor", "Malignant Gynecologic Neoplasm", "malignant gynecologic neoplasm", "female reproductive organ cancer", "Female reprod. system cancer, NOS", "cancer of female reproductive organ", "Female reproductive system cancer, NOS", "malignant neoplasm of female genital organ", "Malignant Female Reproductive System Tumor", "malignant female reproductive system tumor", "Female reproductive neoplasm malignant NOS", "malignant female reproductive organ neoplasm", "Malignant Tumor of Female Reproductive System", "malignant female reproductive system neoplasm", "malignant tumor of female reproductive system", "Malignant Female Reproductive System Neoplasm", "malignant neoplasm of female reproductive organ", "malignant neoplasm of female reproductive system", "Malignant Neoplasm of Female Reproductive System", "Malignant Tumor of the Female Reproductive System", "malignant tumor of the female reproductive system", "malignant neoplasm of the female reproductive system", "Malignant Neoplasm of the Female Reproductive System", "Malignant neoplasm of other and unspecified female genital organs"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "female reproductive organ cancer", "shortest_name_length": 18}
{"curie": "UMLS:C5668302", "names": ["Thymic Carcinoma, NOS", "Thymic Carcinoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thymic Carcinoma, Not Otherwise Specified", "shortest_name_length": 21}
{"curie": "MONDO:0010111", "names": ["Freire-Maia syndrome", "ODONTOTRICHOMELIC SYNDROME", "Odontotrichomelic syndrome", "odontotrichomelic syndrome", "Odontotrichomelic syndrome (disorder)", "Freire-Maia odontotrichomelic syndrome", "odontotrichomelic syndrome (diagnosis)", "odontotrichomelic hypohidrotic dysplasia", "Odontotrichomelic hypohidrotic dysplasia", "TETRAMELIC DEFICIENCIES, ECTODERMAL DYSPLASIA, DEFORMED EARS, AND OTHER ABNORMALITIES", "tetramelic deficiencies, ectodermal dysplasia, deformed ears, and other abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "odontotrichomelic syndrome", "shortest_name_length": 20}
{"curie": "MONDO:0003517", "names": ["mature teratoma", "Mature teratoma", "Mature Teratoma", "Grade 0 Teratoma", "TERATOMA MATURE CYSTIC", "Mature solid teratoma of ovary", "Mature solid teratoma of ovary (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mature teratoma", "shortest_name_length": 15}
{"curie": "MONDO:0040925", "names": ["yaws latent", "latent yaws", "Latent yaws", "latent; yaws", "yaws; latent", "Latent yaws (disorder)", "latent yaws (diagnosis)", "Yaws without clinical manifestations, with positive serology"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "latent yaws", "shortest_name_length": 11}
{"curie": "UMLS:C3272823", "names": ["Colorectal Non-Hodgkin Lymphoma", "Primary Colorectal Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Non-Hodgkin Lymphoma", "shortest_name_length": 31}
{"curie": "UMLS:C0948817", "names": ["Catheter site inflammation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Catheter site inflammation", "shortest_name_length": 26}
{"curie": "MONDO:0002763", "names": ["urethra verrucous carcinoma", "urethral verrucous carcinoma", "Urethral Verrucous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urethral verrucous carcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0008452", "names": ["Fshsma", "FSHSMA", "Spinal Muscular Atrophy, Facioscapulohumeral Type", "spinal muscular atrophy, facioscapulohumeral type", "SPINAL MUSCULAR ATROPHY, FACIOSCAPULOHUMERAL TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal muscular atrophy, facioscapulohumeral type", "shortest_name_length": 6}
{"curie": "UMLS:C4521819", "names": ["I", "Stage I Hilar Cholangiocarcinoma", "Stage I Hilar Cholangiocarcinoma AJCC v8", "Stage I Perihilar Cholangiocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Hilar Cholangiocarcinoma AJCC v8", "shortest_name_length": 1}
{"curie": "UMLS:C0393695", "names": ["Early Childhood Epilepsy, Myoclonic", "Myoclonic Epilepsy, Early Childhood", "Early Childhood, Myoclonic Epilepsy", "Epilepsy, Myoclonic, Early Childhood", "Epilepsy, Early Childhood, Myoclonic", "Myoclonic epilepsy of early childhood", "Myoclonic epilepsy of early childhood (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Early Childhood Epilepsy, Myoclonic", "shortest_name_length": 35}
{"curie": "MONDO:0002914", "names": ["brain stem neoplasm", "Brain Stem Neoplasm", "Childhood Brainstem Tumor", "childhood brainstem tumor", "pediatric brainstem tumor", "Pediatric Brainstem Tumor", "childhood brain stem tumor", "pediatric brainstem cancer", "pediatric brain stem tumor", "childhood brainstem cancer", "Childhood Brain Stem Tumor", "Pediatric Brain Stem Tumor", "childhood tumor of brainstem", "Pediatric Brainstem Neoplasm", "pediatric tumor of Brainstem", "pediatric tumor of brainstem", "childhood brainstem neoplasm", "pediatric brainstem neoplasm", "Pediatric Tumor of Brainstem", "Childhood Tumor of Brainstem", "Childhood Brainstem Neoplasm", "Childhood Tumor of Brain Stem", "Pediatric Tumor of Brain Stem", "childhood tumor of brain stem", "Childhood Brain Stem Neoplasm", "Pediatric Brain Stem Neoplasm", "pediatric brain stem neoplasm", "brainstem cancer of childhood", "childhood brain stem neoplasm", "pediatric tumor of brain stem", "Childhood Neoplasm of Brainstem", "Pediatric Neoplasm of Brainstem", "pediatric neoplasm of brainstem", "childhood neoplasm of brainstem", "pediatric neoplasm of brain stem", "Childhood Neoplasm of Brain Stem", "childhood tumor of the brainstem", "pediatric tumor of the brainstem", "childhood neoplasm of brain stem", "Childhood Tumor of the Brainstem", "Pediatric Neoplasm of Brain Stem", "Pediatric Tumor of the Brainstem", "Childhood Tumor of the Brain Stem", "childhood tumor of the brain stem", "Pediatric Tumor of the Brain Stem", "pediatric tumor of the brain stem", "Pediatric Neoplasm of the Brainstem", "pediatric neoplasm of the brainstem", "childhood neoplasm of the brainstem", "Childhood Neoplasm of the Brainstem", "Childhood Neoplasm of the Brain Stem", "pediatric neoplasm of the brain stem", "Pediatric Neoplasm of the Brain Stem", "childhood neoplasm of the brain stem"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood brain stem neoplasm", "shortest_name_length": 19}
{"curie": "MONDO:0021659", "names": ["MANEC", "Composite carcinoid", "Composite Carcinoid", "composite carcinoid", "adenocarcinoid tumor", "Adenocarcinoid Tumor", "Adenocarcinoid tumor", "Mixed Carcinoid Tumor", "mixed carcinoid tumor", "Adenocarcinoid tumour", "adenocarcinoid neoplasm", "Adenocarcinoid Neoplasm", "Mixed Carcinoid Neoplasm", "mixed carcinoid neoplasm", "[M] Adenocarcinoid tumor", "Composite Carcinoid Tumor", "composite carcinoid tumor", "[M] Adenocarcinoid tumour", "Composite Carcinoid Neoplasm", "composite carcinoid neoplasm", "Mixed carcinoid-adenocarcinoma", "adenocarcinoid tumor (diagnosis)", "Mixed adenoneuroendocrine carcinoma", "combined carcinoid and adenocarcinoma", "composite carcinoid tumor (diagnosis)", "Combined carcinoid and adenocarcinoma", "Combined Carcinoid and Adenocarcinoma", "Combined/mixed carcinoid and adenocarcinoma", "combined carcinoid tumor and adenocarcinoma", "Combined Carcinoid Tumor and Adenocarcinoma", "Composite carcinoid (morphologic abnormality)", "combined carcinoid neoplasm and adenocarcinoma", "Combined Carcinoid Neoplasm and Adenocarcinoma", "Adenocarcinoid tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined carcinoid and adenocarcinoma", "shortest_name_length": 5}
{"curie": "UMLS:C3697063", "names": ["congestive heart failure acute on chronic", "Acute on chronic congestive heart failure", "acute on chronic congestive heart failure", "acute on chronic congestive heart failure (diagnosis)", "Acute exacerbation of chronic congestive heart failure", "congestive heart failure chronic acute exacerbation of", "Acute exacerbation of chronic congestive heart failure (disorder)", "Acute exacerbation of chronic congestive heart failure (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute exacerbation of chronic congestive heart failure", "shortest_name_length": 41}
{"curie": "MONDO:0013224", "names": ["RTPS2", "SMARCA4 familial rhabdoid tumor", "RHABDOID TUMOR PREDISPOSITION SYNDROME 2", "rhabdoid tumor predisposition syndrome 2", "Rhabdoid Tumor Predisposition Syndrome 2", "rhabdoid tumor predisposition syndrome type 2", "familial rhabdoid tumor caused by mutation in SMARCA4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rhabdoid tumor predisposition syndrome 2", "shortest_name_length": 5}
{"curie": "MESH:D002472", "names": ["Cell Transformation, Viral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cell Transformation, Viral", "shortest_name_length": 26}
{"curie": "MONDO:0013678", "names": ["EDICT", "KTCNCT", "EDICT syndrome", "EDICT SYNDROME", "KERATOCONUS WITH CATARACT", "keratoconus with cataract", "Familial keratoconus with cataract", "familial keratoconus with cataract", "KERATOCONUS, FAMILIAL, WITH EARLY-ONSET ANTERIOR POLAR CATARACT", "keratoconus, familial, with early-onset anterior polar cataract", "Autosomal dominant keratoconus with early-onset anterior polar cataract", "Autosomal dominant keratoconus with early-onset anterior polar cataracts", "autosomal dominant keratoconus with early-onset anterior polar cataracts", "Endothelial dystrophy-iris hypoplasia-congenital cataract-stromal thinning syndrome", "endothelial dystrophy-iris hypoplasia-congenital cataract-stromal thinning syndrome", "Endothelial dystrophy, iris hypoplasia, congenital cataract, stromal thinning syndrome", "endothelial dystrophy, iris hypoplasia, congenital cataract, and stromal thinning syndrome", "ENDOTHELIAL DYSTROPHY, IRIS HYPOPLASIA, CONGENITAL CATARACT, AND STROMAL THINNING SYNDROME", "EDICT (endothelial dystrophy, iris hypoplasia, congenital cataract, stromal thinning) syndrome", "Endothelial dystrophy, iris hypoplasia, congenital cataract, stromal thinning syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "EDICT syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0007573", "names": ["FERLK", "Erythroleukemia, Familial", "ERYTHROLEUKEMIA, familial", "DI GUGLIELMO DISEASE, FAMILIAL", "Di Guglielmo disease, familial", "Di Guglielmo Disease, Familial", "leukemia, acute myelogenous, M6", "Leukemia, Acute Myelogenous, M6", "LEUKEMIA, ACUTE MYELOGENOUS, M6", "acute erythroleukemia, familial", "hereditary acute erythroid leukemia", "erythroleukemia, familial, susceptibility to", "ERYTHROLEUKEMIA, FAMILIAL, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythroleukemia, familial, susceptibility to", "shortest_name_length": 5}
{"curie": "MONDO:0700080", "names": ["EPHB4-associated vascular malformation spectrum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "EPHB4-associated vascular malformation spectrum", "shortest_name_length": 47}
{"curie": "UMLS:C0279914", "names": ["stage II childhood HD", "stage II HD, childhood", "childhood HD, stage II", "pediatric HD, stage II", "HD, childhood, stage II", "HD, stage II, childhood", "Stage II Hodgkin Lymphoma", "stage II childhood Hodgkin lymphoma", "Stage II Childhood Hodgkin Lymphoma", "stage II pediatric Hodgkin's disease", "stage II childhood Hodgkin's disease", "Pediatric Hodgkin's Disease Stage II", "Childhood Hodgkin's Disease Stage II", "Stage II Pediatric Hodgkin's Lymphoma", "Stage II Childhood Hodgkin's Lymphoma", "pediatric Hodgkin's disease, stage II", "stage II Hodgkin's disease, childhood", "Childhood Hodgkin's Lymphoma Stage II", "Pediatric Hodgkin's Lymphoma Stage II", "lymphoma, stage II childhood Hodgkin's", "childhood Hodgkin's lymphoma, stage II", "Hodgkin's disease, stage II, childhood", "Hodgkin's lymphoma, stage II, childhood", "Ann Arbor Stage II Childhood Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Childhood Hodgkin Lymphoma", "shortest_name_length": 21}
{"curie": "UMLS:C3274874", "names": ["Significant Arterial Dissection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Significant Arterial Dissection", "shortest_name_length": 31}
{"curie": "MONDO:0015013", "names": ["RP77", "RETINITIS PIGMENTOSA 77", "retinitis pigmentosa 77", "REEP6 retinitis pigmentosa", "retinitis pigmentosa type 77", "retinitis pigmentosa caused by mutation in REEP6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 77", "shortest_name_length": 4}
{"curie": "MONDO:0003694", "names": ["ovary clear cell cystadenofibroma", "ovarian clear cell cystadenofibroma", "Ovarian Clear Cell Cystadenofibroma", "clear cell cystadenofibroma of ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian clear cell cystadenofibroma", "shortest_name_length": 33}
{"curie": "UMLS:C4524727", "names": ["Pathologic Stage IB Gastroesophageal Junction Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IB Gastroesophageal Junction Adenocarcinoma AJCC v8", "shortest_name_length": 68}
{"curie": "UMLS:C1336185", "names": ["Stage IIB Lung Adenocarcinoma", "Stage IIB Adenocarcinoma of Lung", "Stage IIB Adenocarcinoma of the Lung", "Stage IIB Lung Adenocarcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Lung Adenocarcinoma AJCC v7", "shortest_name_length": 29}
{"curie": "MONDO:0010067", "names": ["Splenoportal vascular anomaly", "Splenoportal Vascular Anomalies", "SPLENOPORTAL VASCULAR ANOMALIES", "splenoportal vascular anomalies", "Splenoportal vascular anomaly (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "splenoportal vascular anomalies", "shortest_name_length": 29}
{"curie": "UMLS:C5206577", "names": ["Testicular Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular Diffuse Large B-Cell Lymphoma", "shortest_name_length": 40}
{"curie": "UMLS:C1698998", "names": ["Instillation site discomfort"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Instillation site discomfort", "shortest_name_length": 28}
{"curie": "UMLS:C0162526", "names": ["AIDS, Opportunistic Infection", "Opportunistic Infections in AIDS", "HIV-Related Opportunistic Infection", "Opportunistic Infection, HIV-Related", "AIDS-Related Opportunistic Infection", "HIV-Related Opportunistic Infections", "Infection, HIV-Related Opportunistic", "HIV Related Opportunistic Infections", "AIDS-related opportunistic infections", "AIDS-Related Opportunistic Infections", "Opportunistic Infection, AIDS-Related", "Opportunistic Infections, HIV Related", "Opportunistic Infections, HIV-Related", "AIDS Related Opportunistic Infections", "Infections, HIV-Related Opportunistic", "Opportunistic Infections, AIDS-Related", "Opportunistic Infections, AIDS Related", "AIDS Associated Opportunistic Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Opportunistic Infections", "shortest_name_length": 29}
{"curie": "MONDO:0013920", "names": ["IIAE5", "TRAF3 herpes simplex encephalitis", "herpes simplex encephalitis, susceptibility to, 3", "HERPES SIMPLEX ENCEPHALITIS, SUSCEPTIBILITY TO, 3", "Herpes simplex encephalitis, susceptibility to, type 3", "herpes simplex encephalitis caused by mutation in TRAF3", "encephalopathy, acute, infection-induced, susceptibility to, 5", "ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 5", "encephalopathy, acute, infection-induced (HERPES-specific), susceptibility to, 5", "encephalopathy, acute, infection-induced (Herpes-specific), susceptibility to, 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "herpes simplex encephalitis, susceptibility to, 3", "shortest_name_length": 5}
{"curie": "UMLS:C4527417", "names": ["Basal-Like Prostate Cancer", "Basal-Like Prostate Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Basal-Like Prostate Carcinoma", "shortest_name_length": 26}
{"curie": "UMLS:C0311334", "names": ["GENERALIZED-ONSET SEIZURES", "GENERALIZED CONVULSIVE SEIZURE", "generalized convulsive seizure", "Generalised convulsive epilepsy", "Generalized-onset seizures, NOS", "Generalized Convulsive Epilepsy", "Generalized convulsive epilepsy", "epilepsy generalized convulsive", "Epilepsy, Generalized Convulsive", "Convulsive Epilepsy, Generalized", "Generalized Convulsive Epilepsies", "epilepsy; generalized, convulsive", "generalized; epileptic, convulsive", "Epilepsies, Generalized Convulsive", "Convulsive Epilepsies, Generalized", "Generalized Onset Seizure Disorder", "Seizure Disorder, Generalized Onset", "Generalized convulsive epilepsy, NOS", "Convulsive Generalized Seizure Disorder", "Generalized Seizure Disorder, Convulsive", "Convulsive Seizure Disorder, Generalized", "Seizure Disorder, Convulsive, Generalized", "Seizure Disorder, Generalized, Convulsive", "generalized convulsive seizure (diagnosis)", "Generalized convulsive epilepsy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Generalized convulsive epilepsy", "shortest_name_length": 26}
{"curie": "MONDO:0002200", "names": ["Chondroid Syringoma", "chondroid syringoma", "Eccrine mixed tumor", "eccrine mixed tumor", "Chondroid syringoma", "Mixed tumor of skin", "Mixed tumour of skin", "Eccrine mixed tumour", "Mixed Tumor of the Skin", "benign mixed tumor of skin", "Benign Mixed Tumor of Skin", "eccrine mixed tumor of skin", "Eccrine mixed tumor of skin", "eccrine mixed tumour of skin", "Eccrine mixed tumour of skin", "benign mixed tumor of the skin", "Benign Mixed Tumor of the Skin", "mixed eccrine neoplasm of the skin", "eccrine sweat gland mixed neoplasm", "mixed Eccrine neoplasm of the skin", "Eccrine mixed tumor of skin (disorder)", "Eccrine mixed tumor (morphologic abnormality)", "mixed tumor of the skin (chondroid syringoma)", "eccrine mixed tumor (morphologic abnormality)", "Mixed Tumor of the Skin (Chondroid Syringoma)", "Benign Mixed Tumor of Skin (Chondroid Syringoma)", "benign mixed tumor of skin (chondroid syringoma)", "benign mixed tumor of the skin (chondroid syringoma)", "Benign Mixed Tumor of the Skin (Chondroid Syringoma)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eccrine mixed tumor of skin", "shortest_name_length": 19}
{"curie": "MONDO:0800178", "names": ["deafness, platinum-induced", "platinum-induced ototoxicity", "platinum-related ototoxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "platinum-induced ototoxicity", "shortest_name_length": 26}
{"curie": "UMLS:C0345997", "names": ["Vellus hair cyst", "Vellus Hair Cyst"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vellus Hair Cyst", "shortest_name_length": 16}
{"curie": "UMLS:C5206985", "names": ["Prostate Soft Tissue Neoplasm", "Prostate Mesenchymal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Soft Tissue Neoplasm", "shortest_name_length": 29}
{"curie": "MONDO:0017537", "names": ["bifid hallux, unilateral", "bifid halluces, unilateral", "bifid great toes, unilateral", "Preaxial polydactyly of toes, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Preaxial polydactyly of toes, unilateral", "shortest_name_length": 24}
{"curie": "MONDO:0014699", "names": ["MRD40", "NEDHILD", "MRD40, FORMERLY", "autosomal dominant mental retardation 40", "Mental Retardation, Autosomal Dominant 40", "mental retardation, autosomal dominant 40", "autosomal dominant intellectual disability 40", "intellectual disability, autosomal dominant 40", "mental retardation, autosomal dominant type 40", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 40, FORMERLY", "intellectual disability, autosomal dominant type 40", "autosomal dominant intellectual developmental disorder 40", "autosomal dominant non-syndromic intellectual disability 40", "CHAMP1 autosomal dominant non-syndromic intellectual disability", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 40, FORMERLY", "autosomal dominant non-syndromic intellectual disability caused by mutation in CHAMP1", "NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, IMPAIRED LANGUAGE, AND DYSMORPHIC FEATURES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 40", "shortest_name_length": 5}
{"curie": "EFO:1001289", "names": ["Cholecystitis, Acute"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cholecystitis, Acute", "shortest_name_length": 20}
{"curie": "UMLS:C0474833", "names": ["Benign Stromal Tumor", "Benign stromal tumor", "benign stromal tumors", "Benign stromal tumour", "Benign stromal tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign stromal tumor", "shortest_name_length": 20}
{"curie": "MONDO:0011347", "names": ["Craniosynostosis with Ectopia Lentis", "CRANIOSYNOSTOSIS WITH ECTOPIA LENTIS", "craniosynostosis with ectopia lentis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniosynostosis with ectopia lentis", "shortest_name_length": 36}
{"curie": "MONDO:0008713", "names": ["ae", "AEZ", "enteropathica", "BRANDT SYNDROME", "brandt syndrome", "Brandt syndrome", "Brandt's syndrome", "Danbolt's syndrome", "Danbolt-Cross syndrome", "Danbolt-Closs syndrome", "Danbolt-Close syndrome", "DANBOLT-CLOSS SYNDROME", "inherited zinc deficiency", "Inherited zinc deficiency", "hereditary zinc deficiency", "Primary zinc malabsorption", "Enteropathic acrodermatitis", "acrodermatitis enteropathica", "Acrodermatitis enteropathica", "ACRODERMATITIS ENTEROPATHICA", "Acrodermatitis Enteropathica", "enteropathica; acrodermatitis", "acrodermatitis; enteropathica", "AE - Acrodermatitis enteropathica", "Primary zinc malabsorption syndrome", "Acrodermatitis enteropathica syndrome", "hereditary zinc deficiency (diagnosis)", "Hereditary acrodermatitis enteropathica", "hereditary acrodermatitis enteropathica", "acrodermatitis enteropathica (diagnosis)", "Hereditary acrodermatitis enterohepatica", "Acrodermatitis enteropathica zinc deficiency type", "acrodermatitis enteropathica zinc deficiency type", "ACRODERMATITIS ENTEROPATHICA, ZINC-DEFICIENCY TYPE", "Acrodermatitis Enteropathica, Zinc-Deficiency Type", "Acrodermatitis enteropathica, zinc deficiency type", "acrodermatitis enteropathica, zinc deficiency type", "Hereditary acrodermatitis enteropathica (disorder)", "acrodermatitis enteropathica, zinc-deficiency type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acrodermatitis enteropathica", "shortest_name_length": 2}
{"curie": "MONDO:0021242", "names": ["sublingual gland tumor", "Sublingual Gland Tumor", "Tumor of sublingual gland", "Sublingual Gland Neoplasm", "tumor of sublingual gland", "Tumor of Sublingual Gland", "sublingual gland neoplasm", "Gland Neoplasm, Sublingual", "Sublingual Gland Neoplasms", "Tumour of sublingual gland", "Neoplasm, Sublingual Gland", "Gland Neoplasms, Sublingual", "Neoplasms, Sublingual Gland", "neoplasm of sublingual gland", "Neoplasm of sublingual gland", "Neoplasm of Sublingual Gland", "tumor of the sublingual gland", "Tumor of the Sublingual Gland", "neoplasm of the sublingual gland", "Neoplasm of the Sublingual Gland", "sublingual gland neoplasm (disease)", "Neoplasm of sublingual gland (disorder)", "neoplasm of sublingual gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sublingual gland neoplasm", "shortest_name_length": 22}
{"curie": "MONDO:0001683", "names": ["pancreatic mucinous ductal ectasia", "Pancreatic Mucinous Ductal Ectasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic mucinous ductal ectasia", "shortest_name_length": 34}
{"curie": "MONDO:0007012", "names": ["BSE", "bse", "vCJD", "Variant MCJ", "Mad cow disease", "mad cow disease", "Mad Cow Disease", "Mad Cow Diseases", "bovine spongiform encephalitis", "Bovine Spongiform Encephalitis", "Encephalitis, Bovine Spongiform", "bovine spongiform encephalopathy", "Bovine Spongiform Encephalopathy", "Bovine spongiform encephalopathy", "Variant Creutzfeldt Jakob Disease", "Variant Creutzfeldt-Jakob Disease", "Creutzfeldt-Jakob variant disease", "Spongiform Encephalopathy, Bovine", "Variant Creutzfeldt-Jakob disease", "variant Creutzfeldt-Jakob disease", "Encephalopathy, Bovine Spongiform", "Creutzfeldt-Jakob Disease, Variant", "CREUTZFELDT-JAKOB DISEASE, VARIANT", "Creutzfeldt Jakob Disease, Variant", "New Variant Creutzfeldt-Jakob Disease", "New Variant Creutzfeldt Jakob Disease", "bovine spongiform encephalopathy (BSE)", "BSE (Bovine Spongiform Encephalopathy)", "Creutzfeldt Jakob Disease, New Variant", "Creutzfeldt-Jakob Disease, New Variant", "BSEs (Bovine Spongiform Encephalopathy)", "vCJD - variant Creutzfeldt-Jakob disease", "New variant of Creutzfeldt-Jakob disease", "V CJD (Variant Creutzfeldt Jakob Disease)", "V-CJD (Variant-Creutzfeldt-Jakob Disease)", "Bovine spongiform encephalopathy (disorder)", "Variant Creutzfeldt-Jakob disease (disorder)", "variant Creutzfeldt-Jakob disease (diagnosis)", "nvCJD - New variant of Creutzfeldt-Jakob disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "variant Creutzfeldt-Jakob disease", "shortest_name_length": 3}
{"curie": "MONDO:0005595", "names": ["LXSC", "larynx epidermoid carcinoma", "Larynx Epidermoid Carcinoma", "laryngeal epidermoid carcinoma", "epidermoid carcinoma of larynx", "squamous cell carcinoma larynx", "larynx squamous cell carcinoma", "Laryngeal Epidermoid Carcinoma", "Larynx Squamous Cell Carcinoma", "LARYNGEAL CANCER SQUAMOUS CELL", "Epidermoid Carcinoma of Larynx", "carcinoma cell larynx squamous", "epidermoid carcinoma, laryngeal", "Squamous Cell Carcinoma of Larynx", "Squamous cell carcinoma of larynx", "Laryngeal Squamous Cell Carcinoma", "squamous cell carcinoma of larynx", "Laryngeal squamous cell carcinoma", "laryngeal squamous cell carcinoma", "Epidermoid carcinoma of the Larynx", "epidermoid carcinoma of the larynx", "squamous cell carcinoma, laryngeal", "Epidermoid Carcinoma of the Larynx", "Cancer of the larynx, squamous cell", "Laryngeal Throat Squamous Cell Cancer", "Squamous cell carcinoma of the larynx", "laryngeal throat squamous cell cancer", "Squamous Cell Carcinoma of the Larynx", "squamous cell carcinoma of the larynx", "Primary squamous cell carcinoma of larynx", "Squamous cell carcinoma of larynx (disorder)", "squamous cell carcinoma of larynx (diagnosis)", "Laryngeal Conventional Squamous Cell Carcinoma", "laryngeal malignant carcinoma squamous cell primary", "Primary squamous cell carcinoma of larynx (disorder)", "Primary squamous cell carcinoma of larynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laryngeal squamous cell carcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0018959", "names": ["PAM", "SNEL", "Myotonia permanens", "Myotonia Permanens", "MYOTONIA PERMANENS", "Myotonia Fluctuans", "myotonia permanens", "K-aggravated myotonia", "K+-aggravated myotonia", "Sodium Channel Myotonia", "Sodium channel myotonia", "Myotonia congenita, atypical", "Myotonia Congenita, Atypical", "MYOTONIA CONGENITA, ATYPICAL", "SODIUM CHANNEL MUSCLE DISEASE", "Potassium-Aggravated Myotonia", "Potassium-aggravated myotonia", "Sodium Channel Muscle Disease", "potassium-aggravated myotonia", "Myotonia permanens (disorder)", "Potassium aggravated myotonia", "Potassium Aggravated Myotonia", "MYOTONIA, POTASSIUM-AGGRAVATED", "myotonia permanens (diagnosis)", "Myotonia, Potassium-Aggravated", "Severe Neonatal Episodic Laryngospasm", "LARYNGOSPASM, SEVERE NEONATAL EPISODIC", "Laryngospasm, Severe Neonatal Episodic", "Potassium aggravated myotonia (disorder)", "Acetazolamide responsive myotonia congenita", "MYOTONIA CONGENITA, ACETAZOLAMIDE-RESPONSIVE", "Myotonia congenita, acetazolamide-responsive", "Myotonia Congenita, Acetazolamide-Responsive", "myotonia congenita, atypical, acetazolamide-responsive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "potassium-aggravated myotonia", "shortest_name_length": 3}
{"curie": "UMLS:C0432328", "names": ["Pigmented xerodermoid", "Xerodermoid, pigmented", "Xeroderma pigmentosum XP variant", "Xeroderma pigmentosum, variant form", "Xeroderma pigmentosum, variant form (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Xeroderma pigmentosum, variant form", "shortest_name_length": 21}
{"curie": "MONDO:0010610", "names": ["MHACX", "MICROHYDRANENCEPHALY, X-LINKED", "Morse-Rawnsley-Sargent syndrome", "Morse Rawnsley Sargent syndrome", "Holoprosencephaly with Fetal Akinesia-Hypokinesia Sequence", "HOLOPROSENCEPHALY WITH FETAL AKINESIA/HYPOKINESIA SEQUENCE", "holoprosencephaly with fetal akinesia/hypokinesia sequence", "holoprosencephaly-hypokinesia-congenital contractures syndrome", "holoprosencephaly-fetal akinesia/hypokinesia sequence syndrome", "Holoprosencephaly sequence with hypokinesia and congenital joint contracture syndrome", "Lethal intrauterine growth restriction-cortical malformation-congenital contractures syndrome", "Holoprosencephaly sequence with hypokinesia and congenital joint contracture syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "holoprosencephaly-hypokinesia-congenital contractures syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0346053", "names": ["AFX", "Atypical Fibroxanthoma", "Atypical fibroxanthoma", "fibroxanthoma atypical", "atypical fibroxanthoma", "Fibroxanthosarcoma of skin", "Atypical Skin Fibroxanthoma", "Atypical Fibrous Histiocytoma", "Atypical fibrous histiocytoma", "atypical fibrous histiocytoma", "Atypical Fibroxanthoma of Skin", "Atypical fibroxanthoma of skin", "Atypical Cutaneous Fibroxanthoma", "Atypical Fibroxanthoma of the Skin", "Atypical fibroxanthoma of skin (disorder)", "Superficial Malignant Fibrous Histiocytoma", "Atypical fibrous histiocytoma (morphologic abnormality)", "skin neoplasm malignant fibrohistiocytic atypical fibroxanthoma", "skin neoplasm malignant fibrohistiocytic atypical fibroxanthoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypical fibroxanthoma of skin", "shortest_name_length": 3}
{"curie": "MONDO:0024478", "names": ["Mesenchymal Hamartoma", "Mesenchymal hamartoma", "mesenchymal hamartoma", "Mesenchymal hamartoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mesenchymal hamartoma", "shortest_name_length": 21}
{"curie": "MONDO:0018839", "names": ["acquired schizencephaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired schizencephaly", "shortest_name_length": 23}
{"curie": "MONDO:0007437", "names": ["DD-II", "DTDP2", "Dtdp2", "pulp stones", "Pulpal dysplasia", "pulpal dysplasia", "Pulpal Dysplasia", "PULPAL DYSPLASIA", "Pulpal Dysplasias", "Dysplasia, Pulpal", "Dysplasias, Pulpal", "CORONAL DENTIN DYSPLASIA", "dentin dysplasia type II", "coronal dentin dysplasia", "Dentin dysplasia type II", "dentin dysplasia, type 2", "Coronal Dentin Dysplasia", "Coronal Dentin Dysplasias", "Dentin Dysplasia, Coronal", "Dentin dysplasia, type II", "Dysplasia, Coronal Dentin", "Dentin Dysplasia, Type II", "dentin dysplasia, type II", "DENTIN DYSPLASIA, TYPE II", "Coronal dentine dysplasia", "dentin dysplasia, coronal", "Dentin Dysplasias, Coronal", "Dysplasias, Coronal Dentin", "Dentin Anomalous Dysplasia", "Dentin Anomalous Dysplasias", "Anomalous Dysplasia of Dentin", "ANOMALOUS DYSPLASIA OF DENTIN", "anomalous dysplasia of dentin", "Anomalous dysplasia of dentine", "dentin dyspalsia, Shields type 2", "Dentin Dyspalsia, Shields Type 2", "dentin dysplasia, Shields type 2", "Dentin dyspalsia, Shields type 2", "DENTIN DYSPLASIA, SHIELDS TYPE II", "Dentin Dysplasia, Shields Type II", "Dentine dysplasia - Shield's type II", "Dentin dysplasia, type II (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dentin dysplasia type II", "shortest_name_length": 5}
{"curie": "UMLS:C1735866", "names": ["Abortion of ectopic pregnancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abortion of ectopic pregnancy", "shortest_name_length": 29}
{"curie": "MONDO:0006647", "names": ["ACA Infarct", "Infarct, ACA", "ACA Infarcts", "Infarcts, ACA", "ACA Infarction", "ACA Infarctions", "Infarction, ACA", "Infarctions, ACA", "Anterior Cerebral Artery Stroke", "anterior cerebral artery stroke", "Stroke, Anterior Cerebral Artery", "stroke of anterior cerebral artery", "anterior cerebral artery infarction", "Anterior Cerebral Artery Infarction", "Infarction, Anterior Cerebral Artery", "stroke of anterior cerebral artery (diagnosis)", "Infarction, Anterior Cerebral Artery Circulation", "Infarction, Anterior Cerebral Artery Distribution"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anterior cerebral artery infarction", "shortest_name_length": 11}
{"curie": "MONDO:0007736", "names": ["HPA1", "HPA I RECOGNITION POLYMORPHISM, BETA-GLOBIN-RELATED", "HPA I RECOGNITION polymorphism, BETA-globin-related", "HPA I RECOGNITION polymorphism, BETA-globin-RELATED", "HPA 1 Recognition polymorphism, beta-globin-related", "HPA I RECOGNITION POLYMORPHISM, BETA-GLOBIN-RELATED (disorder)", "RESTRICTION FRAGMENT LENGTH POLYMORPHISM, SICKLE CELL ANEMIA-RELATED", "restriction fragment length polymorphism, sickle cell Anemia-related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HPA 1 Recognition polymorphism, beta-globin-related", "shortest_name_length": 4}
{"curie": "UMLS:C1332271", "names": ["PSIN", "Bowen Disease", "Anal Margin Bowen Disease", "Perianal Skin Bowen Disease", "Perianal Squamous Dysplasia", "Anal Margin Bowen's Disease", "Perianal Skin Bowen's Disease", "Anal Margin Squamous Dysplasia", "Bowen's disease of anal margin", "Perianal Intraepithelial Neoplasia", "Anal Margin Intraepithelial Neoplasia", "Bowen's disease of anal margin (diagnosis)", "Perianal Squamous Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perianal Squamous Intraepithelial Neoplasia", "shortest_name_length": 4}
{"curie": "MONDO:0006037", "names": ["HLS", "hydrolethalus", "Hydrolethalus", "hydrolethalus syndrome", "Hydrolethalus syndrome", "Salonen-Herva-Norio syndrome", "Hydrolethalus syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hydrolethalus syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0002297", "names": ["Adnexal tumor", "adnexal tumor", "Adnexal tumour", "adnexal tumour", "adnexal tumors", "Adnexal Adenoma", "adnexal tumours", "Adenoma of Adnexa", "Skin adnexal tumor", "Skin adnexal tumour", "Skin Appendage Tumor", "skin appendage tumor", "Skin appendage tumor", "skin appendage tumour", "adnexal tumor of skin", "Adnexal Tumor of Skin", "Skin appendage tumour", "Skin adnexal neoplasm", "Skin Appendage Adenoma", "Skin appendage adenoma", "skin appendage neoplasm", "tumor of skin appendage", "Skin Appendage Neoplasm", "Tumor of Skin Appendage", "Skin appendage neoplasm", "adnexal neoplasm of skin", "ADENOMA, ADNEXAL, BENIGN", "Adnexal Neoplasm of Skin", "Adenoma of Skin Appendage", "Epidermal Appendage Tumor", "adnexal tumor of the skin", "epidermal appendage tumor", "Adnexal Tumor of the Skin", "cutaneous appendage tumor", "Epidermal appendage tumor", "cutaneous adnexal neoplasm", "Cutaneous Adnexal Neoplasm", "Neoplasm of Skin Appendage", "Neoplasm of adnexa of skin", "neoplasm of skin appendage", "tumor of the skin appendage", "Tumor of the Skin Appendage", "tumor of cutaneous appendage", "Epidermal Appendage Neoplasm", "Adnexal Neoplasm of the Skin", "cutaneous appendage neoplasm", "Epidermal appendage neoplasm", "Tumor of Epidermal Appendage", "adnexal neoplasm of the skin", "Tumor of epidermal appendage", "tumor of Epidermal appendage", "Tumour of epidermal appendage", "neoplasm of the skin appendage", "Neoplasm of the Skin Appendage", "neoplasm of the skin Appendage", "neoplasm of Epidermal appendage", "Neoplasm of Epidermal Appendage", "neoplasm of cutaneous appendage", "Tumor of epidermal appendage NOS", "cutaneous appendage neoplasm (disease)", "skin neoplasm with adnexal differentiation", "neoplasm of skin with adnexal differentiation", "Neoplasm of skin with adnexal differentiation", "Skin appendage adenoma (morphologic abnormality)", "Neoplasm of skin with adnexal differentiation (disorder)", "Neoplasm of skin with adnexal differentiation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermal appendage tumor", "shortest_name_length": 13}
{"curie": "MONDO:0007354", "names": ["Optic disk coloboma", "Optic disc coloboma", "Optic nerve coloboma", "Coloboma, optic disc", "optic nerve coloboma", "Coloboma of optic disc", "Morning glory syndrome", "COLOBOMA OF OPTIC NERVE", "Coloboma of optic nerve", "coloboma of optic nerve", "coloboma of optic papilla", "Coloboma of optic papilla", "morning glory Disc anomaly", "Congenital optic disc coloboma", "Congenital coloboma of optic disc", "congenital coloboma of optic disc", "coloboma of optic nerve (disease)", "congenital coloboma of the optic nerve", "Congenital coloboma of the optic nerve", "Coloboma of optic disc, unspecified eye", "optic nerve head pits, bilateral congenital", "OPTIC NERVE HEAD PITS, BILATERAL CONGENITAL", "Optic nerve head pits, bilateral congenital", "Congenital coloboma of optic disc (disorder)", "congenital coloboma of optic disc (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coloboma of optic nerve", "shortest_name_length": 19}
{"curie": "UMLS:C0345612", "names": ["Benign Base of Tongue Tumor", "Benign Posterior Tongue Tumor", "Benign tumor of base of tongue", "benign tumor of base of tongue", "Benign Base of Tongue Neoplasm", "Benign Tumor of Base of Tongue", "Benign tumour of base of tongue", "Benign Base of the Tongue Tumor", "Benign Posterior Tongue Neoplasm", "Benign Tumor of Posterior Tongue", "benign neoplasm of base of tongue", "Benign Neoplasm of Base of Tongue", "Benign neoplasm of base of tongue", "Benign Base of the Tongue Neoplasm", "Benign Neoplasm of Posterior Tongue", "Benign Tumor of the Posterior Tongue", "Benign tumor of fixed part of tongue", "Benign tumour of fixed part of tongue", "Benign Tumor of the Base of the Tongue", "Benign Neoplasm of the Posterior Tongue", "Benign tumor of posterior third of tongue", "Benign Neoplasm of the Base of the Tongue", "Benign tumour of posterior third of tongue", "Benign neoplasm of base of tongue (disorder)", "benign neoplasm of base of tongue (diagnosis)", "Benign tumor of tongue posterior to vallate papillae", "Benign tumour of tongue posterior to vallate papillae"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign neoplasm of base of tongue", "shortest_name_length": 27}
{"curie": "MONDO:0008237", "names": ["Stoll-levy-Francfort syndrome", "Stoll Levy Francfort syndrome", "FACIOAURICULORADIAL DYSPLASIA", "facioauriculoradial dysplasia", "Stoll Lévy Francfort syndrome", "Facioauriculoradial dysplasia", "Stoll-Lévy-Francfort syndrome", "Stoll-LC)vy-Francfort syndrome", "phocomelia ectrodactyly deafness sinus arrhythmia", "Phocomelia-ectrodactyly-deafness-sinus arrhythmia syndrome", "phocomelia-ectrodactyly-deafness-sinus arrhythmia syndrome", "Phocomelia-ectrodactyly-hearing loss-sinus arrhythmia syndrome", "Phocomelia, ectrodactyly, deafness and sinus arrhythmia syndrome", "PHOCOMELIA-ECTRODACTYLY, EAR MALFORMATION, DEAFNESS, AND SINUS ARRHYTHMIA", "phocomelia-ectrodactyly, EAR malformation, deafness, and sinus arrhythmia", "Phocomelia-ectrodactyly, ear malformation, deafness, and sinus arrhythmia", "Phocomelia, ectrodactyly, deafness and sinus arrhythmia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phocomelia-ectrodactyly-deafness-sinus arrhythmia syndrome", "shortest_name_length": 29}
{"curie": "UMLS:C0858814", "names": ["hepatitis symptom", "Hepatitis symptom", "hepatitis symptoms"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatitis symptom", "shortest_name_length": 17}
{"curie": "MONDO:0022948", "names": ["Deal Barratt Dillon syndrome", "Fanconi syndrome, ichthyosis, dysmorphism, jaundice and diarrhoea"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Deal Barratt Dillon syndrome", "shortest_name_length": 28}
{"curie": "UMLS:C1322253", "names": ["Infected eczema", "Eczema infected", "infected eczema", "ECZEMA INFECTED", "Infective eczema", "eczema infective", "infective eczema", "Infected eczema (disorder)", "Eczematous dermatitis infected", "Dermatitis, eczematous, infected"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infected eczema", "shortest_name_length": 15}
{"curie": "MONDO:0016280", "names": ["cervical sarcoma", "uterine cervix sarcoma", "sarcoma of cervix uteri", "sarcoma of uterine cervix", "cervical malignant mesenchymal tumor", "malignant mesenchymal tumor of cervix uteri"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sarcoma of cervix uteri", "shortest_name_length": 16}
{"curie": "MONDO:0019838", "names": ["adenohypophysitis", "adenohypophysis inflammation", "lymphocytic adenohypophysitis", "anterior pituitary hypophysitis", "inflammation of adenohypophysis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenohypophysitis", "shortest_name_length": 17}
{"curie": "MONDO:0004077", "names": ["Lumbosacral Lipoma", "lumbosacral lipoma", "sacral region of vertebral column lipoma", "lipoma of sacral region of vertebral column"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lumbosacral lipoma", "shortest_name_length": 18}
{"curie": "UMLS:C0019911", "names": ["hookworm", "hook worm", "HOOK WORM", "hook worms", "Hookworm disease", "HOOKWORM DISEASE", "hookworm disease", "Hookworm diseases", "Hookworm Infection", "hookworm infection", "Hookworm infection", "Infection, Hookworm", "hookworm; infection", "Hookworm Infections", "hookworm infections", "Infections, Hookworm", "Hookworm disease, NOS", "hookworm disease (diagnosis)", "Hookworm disease, unspecified", "Disease due to superfamily Ancylostomatoidea", "DISEASES DUE TO SUPERFAMILY ANCYLOSTOMATOIDEA", "Disease caused by superfamily Ancylostomatoidea", "Disease caused by superfamily Ancylostomatoidea (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hookworm Infections", "shortest_name_length": 8}
{"curie": "UMLS:C0268855", "names": ["bladder hypertrophy", "Bladder hypertrophy", "hypertrophy; bladder", "bladder; hypertrophy", "bladder hypertrophied", "hypertrophy of bladder", "Hypertrophy of bladder", "Hypertrophy of bladder (disorder)", "hypertrophy of bladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypertrophy of bladder", "shortest_name_length": 19}
{"curie": "MONDO:0021727", "names": ["Aberrant subclavian artery", "aberrant subclavian artery", "aberrant; subclavian artery", "Aberrant left subclavian artery", "aberrant left subclavian artery", "SCA - Aberrant subclavian artery", "aberrant right subclavian artery", "congenital malpositioned subclavian artery", "Congenital malpositioned subclavian artery", "congenital malposition of subclavian artery", "aberrant left subclavian artery (diagnosis)", "Congenital malposition of subclavian artery", "Congenital malposition of subclavian artery (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aberrant subclavian artery", "shortest_name_length": 26}
{"curie": "MONDO:0020422", "names": ["aortopulmonary coronary arterial course"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortopulmonary coronary arterial course", "shortest_name_length": 39}
{"curie": "UMLS:C3898623", "names": ["Late Disseminated Lyme Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Late Disseminated Lyme Disease", "shortest_name_length": 30}
{"curie": "UMLS:C5237957", "names": ["Sinonasal Melanoma", "Sinonasal Mucosal Melanoma", "Nasal Cavity and Paranasal Sinus Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Mucosal Melanoma", "shortest_name_length": 18}
{"curie": "MONDO:0011739", "names": ["PNCA1", "Pnca1", "PALLD familial pancreatic carcinoma", "susceptibility to pancreatic cancer 1", "PANCREATIC CANCER, SUSCEPTIBILITY TO, 1", "pancreatic cancer, susceptibility to, 1", "pancreatic cancer, susceptibility to, type 1", "familial pancreatic carcinoma caused by mutation in PALLD"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic cancer, susceptibility to, 1", "shortest_name_length": 5}
{"curie": "MONDO:0000946", "names": ["Vaginismus", "vaginismus", "functional vaginismus", "Nonorganic vaginismus", "Functional vaginismus", "vaginismus; nonorganic", "non-organic vaginismus", "psychogenic vaginismus", "Vaginismus;psychogenic", "Psychologic vaginismus", "Psychogenic Vaginismus", "Non-organic vaginismus", "Psychogenic vaginismus", "psychologic vaginismus", "Vaginismus psychogenic", "nonorganic origin; vaginismus", "Psychologic vaginismus (disorder)", "vaginismus not due to physical condition", "vaginismus not due to physical condition (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "psychologic vaginismus", "shortest_name_length": 10}
{"curie": "UMLS:C5205646", "names": ["Refractory Anaplastic Pleomorphic Xanthoastrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Anaplastic Pleomorphic Xanthoastrocytoma", "shortest_name_length": 51}
{"curie": "UMLS:C4054367", "names": ["Nephrotic Syndrome - SCARB2 Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - SCARB2 Associated", "shortest_name_length": 38}
{"curie": "MONDO:0006718", "names": ["Skin Syphilis", "syphilis; skin", "Syphilis, Skin", "skin; syphilitic", "cutaneous syphilis", "Cutaneous Syphilis", "Syphilis, Cutaneous", "syphilitic skin disorder", "Syphilitic skin disorder", "Syphilitic skin disorder (disorder)", "syphilitic skin disorder (diagnosis)", "Treponema pallidum skin disease caused by bacterial infection", "Treponema pallidum caused skin disease caused by bacterial infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous syphilis", "shortest_name_length": 13}
{"curie": "MONDO:0008062", "names": ["NRCLP1", "CATAPLEXY", "cataplexy", "Cataplexy", "Narcolepsy 1", "narcolepsy 1", "NARCOLEPSY 1", "HCRT narcolepsy", "Cataleptic Attack", "narcolepsy type 1", "Attack, Cataleptic", "Henneberg Syndrome", "Cataleptic Attacks", "Attacks, Cataleptic", "Syndrome, Henneberg", "Cataplexy (disorder)", "Tonelessness Syndrome", "Cataplexy (diagnosis)", "narcoleptic syndrome 1", "Tonelessness Syndromes", "Syndrome, Tonelessness", "Narcoleptic Syndrome 1", "NARCOLEPTIC SYNDROME 1", "Syndromes, Tonelessness", "disorder of brain cataplexy", "narcolepsy caused by mutation in HCRT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "narcolepsy 1", "shortest_name_length": 6}
{"curie": "MONDO:0014373", "names": ["NPHS10", "EMP2 nephrotic syndrome", "nephrotic syndrome type 10", "NEPHROTIC SYNDROME, TYPE 10", "nephrotic syndrome, type 10", "nephrotic syndrome caused by mutation in EMP2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrotic syndrome, type 10", "shortest_name_length": 6}
{"curie": "MONDO:0007634", "names": ["MENTAL RETARDATION, FRA12A TYPE", "mental retardation, FRA12A type", "Mental Retardation, Fra12a Type", "intellectual disability, FRA12A type", "INTELLECTUAL DEVELOPMENTAL DISORDER, FRA12A TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, FRA12A type", "shortest_name_length": 31}
{"curie": "MONDO:0012819", "names": ["DKA", "KPD", "Diabetic Ketoses", "diabetic ketosis", "Diabetic ketosis", "Diabetic Ketosis", "diabetic ketoses", "Acidosis diabetic", "Ketosis, Diabetic", "DIABETIC ACIDOSIS", "ACIDOSIS DIABETIC", "diabetic acidosis", "Ketoses, Diabetic", "Diabetic Acidoses", "Diabetic Acidosis", "Diabetic acidosis", "Acidosis, Diabetic", "Acidoses, Diabetic", "ACIDOSIS, DIABETIC", "KETOACIDOSIS DIABETIC", "Diabetic ketoacidosis", "DIABETIC KETOACIDOSIS", "diabetic ketoacidoses", "Diabetic Ketoacidosis", "Diabetic Ketoacidoses", "diabetic ketoacidosis", "KETOACIDOSIS, DIABETIC", "Ketoacidosis, Diabetic", "Ketoacidoses, Diabetic", "Diabetic acidosis, NOS", "Diabetic keto-acidosis", "Ketoacidosis (diabetic)", "DKA Diabetic Ketoacidosis", "DKA Diabetic Ketoacidoses", "Diabetes with ketoacidosis", "Ketoacidosis, DKA Diabetic", "diabetes with ketoacidosis", "Diabetic Ketoacidosis, DKA", "DKA - diabetic ketoacidosis", "DKA - Diabetic ketoacidosis", "Diabetic ketosis without coma", "Diabetic acidosis without coma", "ketosis-prone diabetes mellitus", "DIABETES MELLITUS, KETOSIS-PRONE", "Ketoacidosis in diabetes mellitus", "diabetes mellitus with ketoacidosis", "Diabetes Mellitus with Ketoacidosis", "Diabetes mellitus with ketoacidosis", "Ketoacidosis due to diabetes mellitus", "Elevated Ketones/Diabetic Ketoacidosis", "diabetes mellitus with ketoacidosis (diagnosis)", "Ketoacidosis due to diabetes mellitus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diabetic ketoacidosis", "shortest_name_length": 3}
{"curie": "MONDO:0016867", "names": ["partial deletion of chromosome 2", "partial monosomy of chromosome 2", "partial deletion of chromosome type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of chromosome 2", "shortest_name_length": 32}
{"curie": "MONDO:0003992", "names": ["childhood sarcoma Botryoides", "Childhood Sarcoma Botryoides", "childhood botryoid rhabdomyosarcoma", "Childhood Botryoid Rhabdomyosarcoma", "pediatric botryoid rhabdomyosarcoma", "botryoid rhabdomyosarcoma of childhood", "botryoid-type embryonal rhabdomyosarcoma", "Botryoid-Type Embryonal Rhabdomyosarcoma", "embryonal-botryoid pediatric rhabdomyosarcoma", "embryonal-botryoid childhood rhabdomyosarcoma", "rhabdomyosarcoma, pediatric embryonal-botryoid", "childhood rhabdomyosarcoma, embryonal-botryoid", "rhabdomyosarcoma, embryonal-botryoid childhood", "pediatric rhabdomyosarcoma, embryonal-botryoid", "rhabdomyosarcoma, childhood embryonal-botryoid", "Childhood Botryoid-Type Embryonal Rhabdomyosarcoma", "childhood botryoid-type embryonal rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood botryoid rhabdomyosarcoma", "shortest_name_length": 28}
{"curie": "UMLS:C0752291", "names": ["Limit Setting Sleep Disorder", "Limit-setting sleep disorder", "Limit-Setting Sleep Disorder", "Limit-Setting Sleep Disorders", "Sleep Disorder, Limit Setting", "Sleep Disorder, Limit-Setting", "Sleep Disorders, Limit-Setting", "disorder of sleep limit-setting", "Limit-setting sleep disorder (disorder)", "Limit-setting sleep disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Limit-Setting Sleep Disorder", "shortest_name_length": 28}
{"curie": "UMLS:C0278952", "names": ["nasopharynx cancer, recurrent", "Relapsed Cancer of Nasopharynx", "Relapsed Nasopharynx Carcinoma", "Relapsed Nasopharyngeal Cancer", "recurrent nasopharyngeal cancer", "Recurrent Cancer of Nasopharynx", "Nasopharyngeal cancer recurrent", "Recurrent Nasopharynx Carcinoma", "Recurrent Nasopharyngeal Cancer", "nasopharyngeal cancer, recurrent", "Nasopharyngeal Cancer, Recurrent", "Relapsed Nasopharyngeal Carcinoma", "Relapsed Carcinoma of Nasopharynx", "Relapsed Cancer of the Nasopharynx", "Recurrent Nasopharyngeal Carcinoma", "Recurrent Carcinoma of Nasopharynx", "Recurrent Cancer of the Nasopharynx", "Relapsed Carcinoma of the Nasopharynx", "Recurrent Carcinoma of the Nasopharynx", "Recurrent Nasopharyngeal Throat Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasopharyngeal cancer recurrent", "shortest_name_length": 29}
{"curie": "MONDO:0019065", "names": ["AMYLOID", "amyloid", "AMYLOIDOSIS", "amyloidosis", "amyloidoses", "Amyloidosis", "Amyloidoses", "Amyloidosis NOS", "amyloid disease", "Amyloid disease", "amyloid diseases", "Amyloidosis, NOS", "amyloid; disorder", "disorder; amyloid", "amyloidosis (disease)", "Amyloidosis (disorder)", "amyloidosis (diagnosis)", "Amyloidosis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyloidosis", "shortest_name_length": 7}
{"curie": "MONDO:0016211", "names": ["non-papillary urothelial carcinoma", "non-papillary transitional cell carcinoma of the bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-papillary transitional cell carcinoma of the bladder", "shortest_name_length": 34}
{"curie": "MONDO:0005833", "names": ["Adenopathy", "adenopathy", "swollen gland", "Swollen Gland", "swollen glands", "lymphangiopathy", "glands, swollen", "lymphadenopathy", "Lymphangiopathy", "Lymphadenopathy", "Lymphangiopathies", "lymphatic disease", "Lymphatic Disease", "Lymphatic disease", "Lymphatic Diseases", "lymphatic disorder", "lymphatic diseases", "Lymphatic disorder", "Disease, Lymphatic", "Lymphatic Disorders", "Lymphangiopathy NOS", "Diseases, Lymphatic", "lymphatic disorders", "Lymphangiopathy, NOS", "Lymphatics--Diseases", "Disorder of lymphatics", "lympoid system disease", "lymphatic system disease", "lymphatic system disorder", "Lymphatic Vessel Diseases", "disease of lympoid system", "disorders lymphatic system", "Lymphatic vessel disorders", "disorder of lymphoid system", "Disorder of lymphoid system", "Disorder of lymphatics, NOS", "disorder of lymphatic vessel", "Disorder of lymphatic system", "disorder of lymphatic system", "Disorder of lymphatic vessel", "disease (or disorder); lymphatic", "DISEASES OF THE LYMPHOID TISSUES", "Disease of lymphatic vessels NOS", "Abnormality of the lymphatic system", "disorder of lymph node and lymphatics", "Disorder of lymphoid system (disorder)", "Disorders of lymph node and lymphatics", "Diseases of lymph node or lymph vessels", "Disorder of lymphatic system (disorder)", "Disorder of lymphatic vessel (disorder)", "disorder of lymphatic vessel (diagnosis)", "disorder of lymphatic system (diagnosis)", "lymphatic part of lymphoid system disease", "disease of lymphatic part of lymphoid system", "disorder of lymphatic part of lymphoid system", "Disorders of lymph node and lymphatics (disorder)", "lymphatic part of lymphoid system disease or disorder", "disease or disorder of lymphatic part of lymphoid system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphatic system disorder", "shortest_name_length": 10}
{"curie": "MONDO:0004229", "names": ["acantholytic variant squamous cell breast carcinoma", "Squamous Cell Breast Carcinoma, Acantholytic Variant", "Breast Squamous Cell Carcinoma, Acantholytic Variant", "squamous cell breast carcinoma, acantholytic variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acantholytic variant squamous cell breast carcinoma", "shortest_name_length": 51}
{"curie": "UMLS:C0431750", "names": ["Pinhole meatus", "meatal stenosis", "Meatal stenosis", "pinhole; meatus", "Meatal Stenosis", "pinpoint; meatus", "meatal stricture", "Meatal stricture", "meatus; pinpoint", "MEATAL STRICTURE", "Pinhole meatus NOS", "URETHRA STENOSIS MEATUS", "Urethral Meatus Stenosis", "Urethral meatal stenosis", "urethral meatus stenosis", "Urethral meatus stenosis", "stenosis; urinary meatus", "urethral meatal stenosis", "Stenosis;urethral meatal", "stricture; urinary meatus", "urinary meatus; stricture", "Pinhole meatus (disorder)", "Stenosis of urinary meatus", "ostium ureteris; stricture", "meatal stenosis (diagnosis)", "stenosis of urethral meatus", "meatus; stricture, urinarius", "Stricture of urethral meatus", "stricture; meatus, urinarius", "Stenosis of urinary meatus (disorder)", "stenosis of urethral meatus (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pinhole meatus", "shortest_name_length": 14}
{"curie": "MONDO:0022998", "names": ["Moore Weaver syndrome", "Distal arthrogryposis Moore Weaver type", "distal arthrogryposis Moore weaver type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal arthrogryposis Moore weaver type", "shortest_name_length": 21}
{"curie": "UMLS:C5447748", "names": ["Epithelioid Myxofibrosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epithelioid Myxofibrosarcoma", "shortest_name_length": 28}
{"curie": "MONDO:0005698", "names": ["cervix; open", "Incompetent cervix", "Incompetent Cervix", "Incompetent;cervix", "CERVIX INCOMPETENT", "cervix incompetent", "incompetent cervix", "cervix incompetence", "incompetence cervix", "Cervix, Incompetent", "Cervix Incompetence", "Incompetent Cervices", "Incompetence, Cervix", "Cervical incompetence", "Cervical Incompetence", "Incompetence;cervical", "cervical incompetence", "Cervices, Incompetent", "Incompetence of cervix", "Cervical Insufficiency", "Cervical insufficiency", "CI - Cervical incompetence", "Incompetence of cervix uteri", "Uterine Cervical Incompetence", "Incompetence, Uterine Cervical", "Cervical Incompetence, Uterine", "UTERUS, CERVICAL OS, INCOMPETENT", "Cervical incompetence (disorder)", "pregnancy; cervical incompetence", "cervical incompetence (diagnosis)", "cervical incompetence in pregnancy", "cervical incompetence in pregnancy (diagnosis)", "Abnormal dilatation of cervix before onset of labor", "Abnormal dilatation of cervix before onset of labour"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical incompetence", "shortest_name_length": 12}
{"curie": "MONDO:0005542", "names": ["Acute Coronary Syndrome", "syndrome acute coronary", "acute coronary syndrome", "Acute coronary syndrome", "syndrome, acute coronary", "coronary syndrome, acute", "Coronary Syndrome, Acute", "Acute Coronary Syndromes", "Syndrome, Acute Coronary", "acute coronary syndromes", "syndromes, acute coronary", "coronary syndromes, acute", "Syndromes, Acute Coronary", "Coronary Syndromes, Acute", "ACS - Acute coronary syndrome", "Acute coronary syndrome (disorder)", "acute coronary syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute coronary syndrome", "shortest_name_length": 23}
{"curie": "UMLS:C0686593", "names": ["Myeloid leukemia in remission", "Myeloid Leukemia in Remission", "Myeloid leukaemia in remission", "Myeloid leukemia (in remission)", "Myelocytic Leukemia in Remission", "leukemia myelogenous in remission", "myelogenous leukemia in remission", "Myelogenous Leukemia in Remission", "Myeloid leukemia, NOS, in remission", "Myeloid leukemia NOS (in remission)", "Myeloid leukaemia NOS (in remission)", "Myeloid leukaemia, NOS, in remission", "Myeloid leukemia in remission (disorder)", "Unspecified myeloid leukemia in remission", "Unspecified myeloid leukemia, in remission", "Unspecified myeloid leukaemia in remission", "Myeloid leukemia, unspecified in remission", "Myeloid leukemia, unspecified, in remission", "Myeloid leukaemia, unspecified, in remission", "myelogenous leukemia in remission (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myeloid Leukemia in Remission", "shortest_name_length": 29}
{"curie": "UMLS:C3272533", "names": ["Small Intestinal MANEC", "Small Intestinal Mixed Adenoneuroendocrine Cancer", "Small Intestinal Mixed Adenoneuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Intestinal Mixed Adenoneuroendocrine Carcinoma", "shortest_name_length": 22}
{"curie": "UMLS:C4521795", "names": ["Stage II Gastric (Stomach) Cancer", "Postneoadjuvant Therapy Stage II Gastric Cancer AJCC v8", "Postneoadjuvant Therapy Stage II Gastric Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postneoadjuvant Therapy Stage II Gastric Cancer AJCC v8", "shortest_name_length": 33}
{"curie": "UMLS:C1834969", "names": ["Metaphyseal Dysplasia with Maxillary Hypoplasia and Brachydactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metaphyseal Dysplasia with Maxillary Hypoplasia and Brachydactyly", "shortest_name_length": 65}
{"curie": "UMLS:C5557377", "names": ["Vaginal Solitary Fibrous Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Solitary Fibrous Tumor", "shortest_name_length": 30}
{"curie": "UMLS:C0855010", "names": ["PNET of bone recurrent", "Recurrent PNET of Bone", "Recurrent Neuroepithelioma of Bone", "Peripheral neuroepithelioma of bone recurrent", "Recurrent Peripheral Primitive Neuroectodermal Tumor of Bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peripheral neuroepithelioma of bone recurrent", "shortest_name_length": 22}
{"curie": "UMLS:C0153378", "names": ["palate cancer", "Palate Cancer", "cancer palate", "Cancer of palate", "Cancer of Palate", "Cancer of the Palate", "CA - Cancer of palate", "Malignant Palate Tumor", "Malignant tumor of palate", "Malignant Tumor of Palate", "Malignant Palate Neoplasm", "malignant tumor of palate", "Malignant palate neoplasm", "Malignant tumour of palate", "Malignant neoplasm of palate", "malignant neoplasm of palate", "Malignant Neoplasm of Palate", "Malignant Tumor of the Palate", "Malignant Neoplasm of the Palate", "Malignant tumor of roof of mouth", "Malignant tumour of roof of mouth", "Malignant neoplasm of palate, NOS", "Malignant neoplasm of roof of mouth", "Malignant tumor of palate (disorder)", "malignant neoplasm of palate (diagnosis)", "Malignant neoplasm of palate, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant tumor of palate", "shortest_name_length": 13}
{"curie": "UMLS:C4525060", "names": ["Refractory Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Lymphoma", "shortest_name_length": 19}
{"curie": "MONDO:0015782", "names": ["dysmorphism-cleft palate-loose skin syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dysmorphism-cleft palate-loose skin syndrome", "shortest_name_length": 44}
{"curie": "UMLS:C1868710", "names": ["Bronchial secretion retention"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bronchial secretion retention", "shortest_name_length": 29}
{"curie": "UMLS:C4525133", "names": ["Stage I Rectal Cancer", "Stage I Rectal Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Rectal Cancer AJCC v8", "shortest_name_length": 21}
{"curie": "UMLS:C0854836", "names": ["Angiocentric Lymphoma Stage II", "Stage II Angiocentric Lymphoma", "Angiocentric lymphoma stage II", "Nasal T-cell lymphoma stage II", "Polymorphic reticulosis stage II", "Stage II Nasal Type NK/T-Cell Lymphoma", "Ann Arbor Stage II Nasal Type NK/T-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Angiocentric lymphoma stage II", "shortest_name_length": 30}
{"curie": "UMLS:C0521799", "names": ["Ectopic Calcitonin Secretion", "Ectopic Calcitonin Production", "Ectopic calcitonin production", "Ectopic Calcitonin Secretion Syndrome", "Ectopic calcitonin production (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ectopic calcitonin production", "shortest_name_length": 28}
{"curie": "UMLS:C4727217", "names": ["Metastatic Cervical Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Cervical Carcinoma", "shortest_name_length": 29}
{"curie": "UMLS:C0266524", "names": ["eye; dysplasia", "dysplasia; eye", "Dysplasia of eye", "Dysplasia of eye (disorder)", "congenital dysplasia of eye", "congenital dysplasia of eye (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dysplasia of eye", "shortest_name_length": 14}
{"curie": "UMLS:C4524962", "names": ["stage I small intestine cancer", "Stage I Small Intestinal Adenocarcinoma", "Stage I Small Intestinal Adenocarcinoma AJCC v8", "stage I small intestinal adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Small Intestinal Adenocarcinoma AJCC v8", "shortest_name_length": 30}
{"curie": "UMLS:C0151859", "names": ["POLYSEROSITIS", "polyserositis", "Polyserositis", "Bamberger's disease", "Polyserositis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Polyserositis", "shortest_name_length": 13}
{"curie": "MONDO:8000019", "names": ["BRV1", "Vertigo, Benign Recurrent, 1", "VERTIGO, BENIGN RECURRENT, 1", "vertigo, benign recurrent, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vertigo, benign recurrent, 1", "shortest_name_length": 4}
{"curie": "MONDO:0002295", "names": ["glomus skin tumor", "Glomus Skin Tumor", "skin glomus tumor", "Skin Glomus Tumor", "skin glomus tumour", "Glomus skin neoplasm", "skin glomus neoplasm", "glomus tumor of skin", "Skin Glomus Neoplasm", "Glomus Skin Neoplasm", "glomus skin neoplasm", "Glomus tumor of skin", "Glomus Tumor of Skin", "Glomus tumour of skin", "Glomus Neoplasm of Skin", "glomus neoplasm of skin", "Glomus Tumor of the Skin", "glomus tumor of the skin", "zone of skin glomus tumor", "Glomus Neoplasm of the Skin", "glomus neoplasm of the skin", "Glomus tumor of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin glomus tumor", "shortest_name_length": 17}
{"curie": "UMLS:C0282507", "names": ["heat stress", "Heat Illness", "Illness, Heat", "Heat Illnesses", "Heat Stress Syndrome", "Heat Stress Disorder", "Heat Stress Syndromes", "Stress Disorder, Heat", "Stress Syndrome, Heat", "Heat Stress Disorders", "Stress Disorders, Heat"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Heat Stress Disorders", "shortest_name_length": 11}
{"curie": "MONDO:0014555", "names": ["PSS3", "PSS type A", "PEELING SKIN SYNDROME 3", "peeling skin syndrome 3", "peeling skin syndrome type A", "peeling skin syndrome type 3", "generalized deciduous skin type A", "generalized peeling skin syndrome type A", "non-inflammatory peeling skin syndrome type A", "non-inflammatory generalized peeling skin syndrome type A."], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peeling skin syndrome type A", "shortest_name_length": 4}
{"curie": "MONDO:0008209", "names": ["CHAR", "Char", "CHAR syndrome", "CHAR SYNDROME", "Char syndrome", "PATENT DUCTUS ARTERIOSUS WITH FACIAL DYSMORPHISM AND ABNORMAL FIFTH DIGITS", "Patent ductus arteriosus with facial dysmorphism and abnormal fifth digits", "Patent Ductus Arteriosus With Facial Dysmorphism And Abnormal Fifth Digits", "patent ductus arteriosus with facial dysmorphism and abnormal fifth digits", "patent ductus arteriosus with Facial Dysmorphism and abnormal fifth digits", "Patent ductus arteriosus with facial dysmorphism and abnormal fifth digits (disorder)", "patent ductus arteriosus with facial dysmorphism and abnormal fifth digits (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Char syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0017240", "names": ["acrodysostosis with multiple hormone resistance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acrodysostosis with multiple hormone resistance", "shortest_name_length": 47}
{"curie": "MONDO:0010448", "names": ["MYMY4", "syndromic Moyamoya disease", "SYNDROMIC MOYAMOYA DISEASE", "moyamoya disease 4, X-linked recessive", "CHROMOSOME Xq28 DELETION SYNDROME, 3.4-KB", "chromosome Xq28 deletion syndrome, 3.4-Kb", "Moyamoya disease-short stature-facial dysmorphism-hypergonadotropic hypogonadism", "moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome", "Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism, and facial dysmorphism", "MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM, AND FACIAL DYSMORPHISM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0004390", "names": ["IOP decreased", "hypotony; eye", "decreased iop", "eye; hypotony", "ocular hypotony", "Ocular hypotony", "Ocular Hypotony", "hypotony of eye", "Hypotony of eye", "hypotony ocular", "Hypotony, Ocular", "Globe hypotension", "Ocular Hypotension", "ocular hypotension", "Hypotension, Ocular", "Hypotony of eye, NOS", "low intraocular pressure", "Low intraocular pressure", "Intraocular pressure low", "Hypotony of eye (disorder)", "hypotony of eye (diagnosis)", "Unspecified hypotony of eye", "Hypotony of eye, unspecified", "Lowered intraocular pressure", "decrease intraocular pressure", "INTRAOCULAR PRESSURE DECREASE", "Decreased intraocular pressure", "decreased intraocular pressure", "Intraocular pressure decreased", "Intraocular Pressure Decreased", "intraocular pressure was decreased", "Decreased intraocular pressure (finding)", "decreased intraocular pressure (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ocular hypotension", "shortest_name_length": 13}
{"curie": "MONDO:0002590", "names": ["combined thymoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined thymoma", "shortest_name_length": 16}
{"curie": "UMLS:C0478251", "names": ["Superficial injury of abdomen, lower back and pelvis", "Superficial Injury of Abdomen, Lower Back and Pelvis", "Superficial injury of abdomen, lower back and pelvis, part unspecified", "Superficial injury of abdomen, lower back and pelvis, part unspecified, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Superficial injury of abdomen, lower back and pelvis, part unspecified", "shortest_name_length": 52}
{"curie": "UMLS:C4330936", "names": ["Parietal Lobe and Occipital Lobe Ependymal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parietal Lobe and Occipital Lobe Ependymal Tumor", "shortest_name_length": 48}
{"curie": "UMLS:C4725030", "names": ["Refractory Nasopharyngeal Carcinoma", "Refractory Nasopharyngeal Throat Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Nasopharyngeal Carcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C0033054", "names": ["Late Effects, Prenatal Exposure", "Prenatal Exposure Delayed Effects", "Delayed Effects, Prenatal Exposure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prenatal Exposure Delayed Effects", "shortest_name_length": 31}
{"curie": "MONDO:0019383", "names": ["ADE", "ADEM", "Acute disseminated encephalitis", "acute disseminated encephalitis", "MYELINOCLASIS, PERIVASCULAR, ACUTE", "acute disseminated encephalomyelitis", "Acute Disseminated Encephalomyelitis", "Acute disseminated encephalomyelitis", "acute; disseminated encephalomyelitis", "Disseminated Encephalomyelitis, Acute", "Encephalomyelitis, Acute Disseminated", "encephalomyelitis; acute disseminated", "Acute Disseminated Encephalomyelitides", "ENCEPHALOMYELITIS, DISSEMINATED, ACUTE", "ADEM - Acute disseminated encephalomyelitis", "Acute disseminated encephalomyelitis (disorder)", "acute disseminated encephalomyelitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute disseminated encephalomyelitis", "shortest_name_length": 3}
{"curie": "MONDO:0004749", "names": ["myocardium cancer", "tumor of myocardium", "tumor of Myocardium", "cancer of myocardium", "malignant myocardial tumor", "Malignant Myocardial Tumor", "malignant Myocardial tumor", "Malignant Myocardial Neoplasm", "malignant myocardial neoplasm", "Malignant tumor of myocardium", "malignant tumor of myocardium", "malignant myocardium neoplasm", "Malignant Tumor of Myocardium", "Malignant tumour of myocardium", "Malignant Neoplasm of Myocardium", "malignant neoplasm of myocardium", "Malignant neoplasm of myocardium", "malignant tumor of the myocardium", "Malignant Tumor of the Myocardium", "Malignant Neoplasm of the Myocardium", "malignant neoplasm of the myocardium", "Malignant tumor of myocardium (disorder)", "malignant neoplasm of myocardium (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myocardium cancer", "shortest_name_length": 17}
{"curie": "MONDO:0018510", "names": ["small intestine NET", "NET of the small intestine", "Neuroendocrine tumor of small bowel", "neuroendocrine tumor of small bowel", "small Intestine neuroendocrine tumor", "Small intestine neuroendocrine tumor", "small intestine neuroendocrine tumor", "Small intestine neuroendocrine tumour", "small intestine neuroendocrine neoplasm", "Small Intestine Neuroendocrine Neoplasm", "small intestinal neuroendocrine neoplasm", "Small Intestinal Neuroendocrine Neoplasm", "neuroendocrine neoplasm of small intestine", "Neuroendocrine neoplasm of small intestine", "Neuroendocrine tumor of the small intestine", "neuroendocrine tumor of the small intestine", "Neuroendocrine neoplasm of the small intestine", "neuroendocrine neoplasm of the small intestine", "Neuroendocrine neoplasm of small intestine (disorder)", "small intestine neuroendocrine tumor, well differentiated, low or intermediate grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small intestine neuroendocrine neoplasm", "shortest_name_length": 19}
{"curie": "UMLS:C0259768", "names": ["Burst wound", "Wound rupture", "wound rupture", "Wound opened up", "Wound dehiscence", "dehiscence wound", "wound disruption", "WOUND DEHISCENCE", "Wound Disruption", "Wound Dehiscence", "wound dehiscence", "Wound;disruption", "Dehiscence;wound", "dehiscence wounds", "Disruption of wound", "dehiscence of wound", "Dehiscence of wound", "disruption of wound", "Wound surface unfolded", "Disruption of wound NOS", "Wound dehiscence (disorder)", "Wound reopened - observation", "wound dehiscence (diagnosis)", "disruption of wound (diagnosis)", "Disruption of wound, unspecified", "dehiscence of wound (physical finding)", "Wound dehiscence (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wound dehiscence", "shortest_name_length": 11}
{"curie": "MONDO:0023165", "names": ["florid cystic endosalpingiosis", "cystic endosalpingiosis of the uterus", "Cystic endosalpingiosis of the uterus", "Florid cystic endosalpingiosis of the uterus", "florid cystic endosalpingiosis of the uterus", "intramural florid cystic endosalpingiosis of the uterus", "intramural florid cystic endosalpingiosis in lower uterine segment of the uterus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "florid cystic endosalpingiosis of the uterus", "shortest_name_length": 30}
{"curie": "UMLS:C0854896", "names": ["Primary Malignant Hemangiopericytoma", "Malignant Hemangiopericytoma Nonmetastatic", "Malignant hemangiopericytoma non-metastatic", "Non-Metastatic Malignant Hemangiopericytoma", "Malignant haemangiopericytoma non-metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant haemangiopericytoma non-metastatic", "shortest_name_length": 36}
{"curie": "MONDO:0014579", "names": ["SLSN8", "Senior-Loken syndrome 8", "SENIOR-LOKEN SYNDROME 8", "SENIOR-Loken syndrome 8", "WDR19 Senior-Loken syndrome", "Senior-Loken syndrome type 8", "Senior-Loken syndrome caused by mutation in WDR19"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Senior-Loken syndrome 8", "shortest_name_length": 5}
{"curie": "UMLS:C4331476", "names": ["Unresectable Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Liposarcoma", "shortest_name_length": 24}
{"curie": "MONDO:0010035", "names": ["SLOS", "SLO SYNDROME", "RSH Syndrome", "RSH SYNDROME", "SLO Syndrome", "rsh syndrome", "RSH syndrome", "SLO syndrome", "RSH Syndromes", "Syndrome, SLO", "SLO Syndromes", "Syndrome, RSH", "Smith syndrome", "smith syndrome", "syndrome smith", "Syndromes, SLO", "Syndromes, RSH", "smith syndromes", "RSH-SLO Syndrome", "RSH SLO Syndrome", "RSH-SLO Syndromes", "Smith-Lemli-Opitz", "Smith-Lemli-Opitz syndrome", "smith-lemli-opitz syndrome", "SMITH-LEMLI-OPITZ SYNDROME", "Smith Lemli Opitz syndrome", "Smith Lemli Opitz Syndrome", "smith lemli opitz syndrome", "Smith-Lemli-Opitz Syndrome", "Smith-Opitz-Inborn syndrome", "Smith-Opitz-inborn syndrome", "Smith-Lemli-Opitz syndrome I", "lethal acrodysgenital syndrome", "LETHAL ACRODYSGENITAL SYNDROME", "RSH/Smith-Lemli-Opitz syndrome", "Smith-Lemli-Opitz syndrome (disorder)", "Smith-Lemli-Opitz syndrome (diagnosis)", "RSH/Smith-Lemli-Opitz (RSH/SLO) syndrome", "7-Dehydrocholesterol reductase deficiency", "7-dehydrocholesterol reductase deficiency", "Smith-Lemli-Opitz (SLO) syndrome I (SLOS I)", "Hyperotosis Corticalis Generalisata Familiaris", "RUTLEDGE LETHAL MULTIPLE CONGENITAL ANOMALY SYNDROME", "Rutledge lethal multiple congenital anomaly syndrome", "POLYDACTYLY, SEX REVERSAL, RENAL HYPOPLASIA, AND UNILOBAR LUNG", "Polydactyly, Sex Reversal, Renal Hypoplasia, And Unilobar Lung", "polydactyly, sex reversal, renal hypoplasia, and unilobar lung", "polydactyly, sex reversal, renal hypoplasia, and unilobular lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Smith-Lemli-Opitz syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C1332839", "names": ["Breast Carcinoid Tumor", "Carcinoid Tumor of Breast", "Primary Breast Carcinoid Tumor", "Breast Neuroendocrine Tumor G1", "Primary Carcinoid Tumor of Breast", "Primary Carcinoid Tumor of the Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Neuroendocrine Tumor G1", "shortest_name_length": 22}
{"curie": "UMLS:C5236145", "names": ["Radiation-Induced Malignant Peripheral Nerve Sheath Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radiation-Induced Malignant Peripheral Nerve Sheath Tumor", "shortest_name_length": 57}
{"curie": "UMLS:C5557166", "names": ["Stage II Cervical Cancer AJCC v9", "Stage II Cervical Carcinoma AJCC v9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Cervical Cancer AJCC v9", "shortest_name_length": 32}
{"curie": "MONDO:0004636", "names": ["Stage 0 Lip Cancer", "stage 0 Lip cancer", "Stage 0 Lip Carcinoma", "lip in situ carcinoma", "stage 0 lip carcinoma", "Stage 0 Cancer of Lip", "stage 0 cancer of Lip", "lip carcinoma in situ", "Lip Carcinoma in situ", "Carcinoma in situ of Lip", "carcinoma in situ of lip", "Stage 0 Carcinoma of Lip", "Carcinoma in situ of lip", "stage 0 carcinoma of Lip", "stage 0 cancer of the Lip", "Stage 0 Cancer of the Lip", "stage 0 Lip cancer aJCC v7", "Stage 0 Lip Cancer AJCC v7", "Stage 0 Lip Cancer AJCC v6", "stage 0 Lip cancer aJCC v6", "Carcinoma in situ of the Lip", "stage 0 carcinoma of the Lip", "Stage 0 Carcinoma of the Lip", "carcinoma in situ of the Lip", "Carcinoma in situ of lip, NOS", "lip neoplasm carcinoma in situ", "stage 0 Lip cancer aJCC v6 and v7", "Stage 0 Lip Cancer AJCC v6 and v7", "Carcinoma in situ of lip (disorder)", "carcinoma in situ of lip (diagnosis)", "Carcinoma in situ of lip, oral cavity and pharynx", "Carcinoma in situ of lip, oral cavity, and pharynx"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lip carcinoma in situ", "shortest_name_length": 18}
{"curie": "MONDO:0015762", "names": ["PFIC", "byler syndrome", "Byler syndrome", "byler's syndrome", "Byler's syndrome", "PFIC; Byler disease", "Fatal intrahepatic cholestasis", "cholestasis familial intrahepatic", "Familial intrahepatic cholestasis", "Progressive intrahepatic cholestasis", "Progressive familial intrahepatic cholestasis", "progressive familial intrahepatic cholestasis", "Progressive Familial Intrahepatic Cholestasis", "cholestasis, progressive familial intrahepatic", "Progressive intrahepatic cholestasis (disorder)", "Fatal familial intrahepatic cholestasis syndrome", "PFIC - progressive familial intrahepatic cholestasis", "progressive familial intrahepatic cholestasis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive familial intrahepatic cholestasis", "shortest_name_length": 4}
{"curie": "UMLS:C4724394", "names": ["Metastatic Soft Tissue Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Soft Tissue Sarcoma", "shortest_name_length": 30}
{"curie": "UMLS:C0432417", "names": ["Trisomy 21, meiotic nondisjunction", "Trisomy 21- meiotic nondisjunction", "Trisomy 21, Meiotic Nondisjunction", "trisomy; 21, meiotic nondisjunction", "Trisomy 21- meiotic nondisjunction (disorder)", "trisomy; syndrome, 21, meiotic nondisjunction", "syndrome; trisomy, 21, meiotic nondisjunction", "trisomy 21 (down syndrome) nonmosaicisim (meiotic nondisjunction)", "trisomy 21 (down syndrome) nonmosaicisim (meiotic nondisjunction) (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Trisomy 21, Meiotic Nondisjunction", "shortest_name_length": 34}
{"curie": "MONDO:0019483", "names": ["MTX-LPD", "Methotrexate-Related Lymphoproliferation", "methotrexate-associated lymphoproliferation", "MTX-associated lymphoproliferative disorders", "Methotrexate-Related Lymphoproliferative Disorder", "lymphoproliferative disease caused by methotrexate", "Lymphoproliferative disorder caused by methotrexate", "methotrexate-associated lymphoproliferative disorder", "Methotrexate-associated lymphoproliferative disorder", "methotrexate-associated lymphoproliferative disorders", "Methotrexate-associated lymphoproliferative disorders", "Lymphoproliferative disorder caused by methotrexate (disorder)", "lymphoproliferative disease caused by methotrexate (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "methotrexate-associated lymphoproliferative disorders", "shortest_name_length": 7}
{"curie": "UMLS:C5555951", "names": ["Broad Ligament Leiomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Broad Ligament Leiomyosarcoma", "shortest_name_length": 29}
{"curie": "MONDO:0001063", "names": ["cardia cancer", "Ca cardia - stomach", "cardia of stomach cancer", "Malignant tumor of cardia", "Malignant tumour of cardia", "cancer of cardia of stomach", "Malignant neoplasm of cardia", "Malignant tumor of cardia (disorder)", "malignant tumor of cardia of stomach", "malignant cardia of stomach neoplasm", "Malignant neoplasm of cardiac orifice", "Malignant neoplasm of cardia of stomach", "malignant neoplasm of cardia of stomach", "Malignant neoplasm of cardio-esophageal junction", "malignant neoplasm of cardia of stomach (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardia cancer", "shortest_name_length": 13}
{"curie": "UMLS:C0855035", "names": ["Relapsed Malignant Fibrous Histiocytoma", "Malignant fibrous histiocytoma recurrent", "Recurrent Malignant Fibrous Histiocytoma", "Malignant Fibrous Histiocytoma Recurrent", "Recurrent Unclassified Pleomorphic Sarcoma", "Recurrent Undifferentiated Pleomorphic Sarcoma", "Recurrent Unclassified Pleomorphic Sarcoma (Formerly Recurrent \"MFH\")", "Recurrent Unclassified Pleomorphic Sarcoma (Formerly Recurrent \"Malignant Fibrous Histiocytoma\")"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant fibrous histiocytoma recurrent", "shortest_name_length": 39}
{"curie": "MONDO:0012752", "names": ["ANIB6", "intracranial berry aneurysm 6", "aneurysm, intracranial BERRY, 6", "Aneurysm, Intracranial Berry, 6", "aneurysm, intracranial berry, 6", "ANEURYSM, INTRACRANIAL BERRY, 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aneurysm, intracranial berry, 6", "shortest_name_length": 5}
{"curie": "MONDO:0011808", "names": ["Ccnp", "CCNP", "CTRCT27", "cataract 27", "CATARACT 27", "cataract type 27", "CATARACT, NUCLEAR PROGRESSIVE", "Cataract, Nuclear Progressive", "cataract 27 nuclear progressive", "CATARACT 27, NUCLEAR PROGRESSIVE", "cataract 27, nuclear progressive", "Cataract, Congenital, Nuclear Progressive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 27", "shortest_name_length": 4}
{"curie": "MONDO:0016220", "names": ["congenital trismus", "Congenital trismus", "congenital temporomandibular joint ankylosis", "Congenital temporomandibular joint ankylosis", "Congenital ankylosis of temporomandibular joint", "Congenital ankylosis of temporomandibular joint (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital temporomandibular joint ankylosis", "shortest_name_length": 18}
{"curie": "MONDO:0004080", "names": ["Glottis Epidermoid Carcinoma", "Glottic Epidermoid Carcinoma", "glottic epidermoid carcinoma", "glottis epidermoid carcinoma", "Glottis Squamous Cell Carcinoma", "epidermoid carcinoma of glottis", "Epidermoid Carcinoma of Glottis", "Glottic Squamous Cell Carcinoma", "glottis squamous cell carcinoma", "glottic squamous cell carcinoma", "squamous cell carcinoma of glottis", "Squamous Cell Carcinoma of Glottis", "epidermoid carcinoma of the glottis", "Epidermoid Carcinoma of the Glottis", "Epidermoid carcinoma of the Glottis", "Squamous Cell Carcinoma of the Glottis", "squamous cell carcinoma of the glottis", "squamous cell carcinoma of glottis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glottis squamous cell carcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0020771", "names": ["SCAN", "spinocerebellar ataxia, autosomal recessive, with axonal neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia, autosomal recessive, with axonal neuropathy", "shortest_name_length": 4}
{"curie": "MONDO:0010502", "names": ["MRXS99F", "USP9X X-linked syndromic intellectual disability", "female-restricted syndromic X-linked mental retardation 99", "mental retardation, X-linked 99, syndromic, female-restricted", "MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED", "female-restricted syndromic X-linked intellectual disability 99", "intellectual disability, X-linked 99, syndromic, female-restricted", "X-linked syndromic intellectual disability caused by mutation in USP9X", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED", "intellectual developmental disorder, X-linked 99, syndromic, female-restricted, X-linked dominant", "X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 99, syndromic, female-restricted", "shortest_name_length": 7}
{"curie": "UMLS:C1868999", "names": ["Cerebral microbleeding", "Cerebral microhemorrhage", "Cerebral microhaemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebral microhaemorrhage", "shortest_name_length": 22}
{"curie": "MONDO:0015467", "names": ["Craniosynostosis Philadelphia type", "CRANIOSYNOSTOSIS, PHILADELPHIA TYPE", "Craniosynostosis, Philadelphia type", "Craniosynostosis, Philadelphia Type", "craniosynostosis, Philadelphia type", "Craniosynostosis Philadelphia type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniosynostosis, Philadelphia type", "shortest_name_length": 34}
{"curie": "MONDO:0032850", "names": ["NOCGUS", "NEUROOCULOCARDIOGENITOURINARY SYNDROME", "neurooculocardiogenitourinary syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurooculocardiogenitourinary syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0030529", "names": ["AGM10", "agammaglobulinemia 10", "AGAMMAGLOBULINEMIA 10, AUTOSOMAL DOMINANT", "agammaglobulinemia 10, autosomal dominant", "AGAMMAGLOBULINEMIA, AUTOSOMAL DOMINANT, DUE TO SPI1 DEFECT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "agammaglobulinemia 10, autosomal dominant", "shortest_name_length": 5}
{"curie": "UMLS:C3203730", "names": ["Infectious pleural effusion", "Infectious pleural effusion (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infectious pleural effusion", "shortest_name_length": 27}
{"curie": "MONDO:0006519", "names": ["rectum cancer", "rectal cancer", "cancer of rectum", "carcinoma of rectum", "Neoplasm malig;rectum", "malignant rectal tumor", "malignant Rectal tumor", "Malignant Rectal Tumor", "malignant rectum tumor", "carcinoma of the rectum", "malignant rectum neoplasm", "rectal cancer (diagnosis)", "rectal neoplasm malignant", "Malignant Tumor of Rectum", "Malignant Rectal Neoplasm", "malignant rectal neoplasm", "malignant tumor of rectum", "Malignant tumor of rectum", "Malignant tumour of rectum", "Malignant neoplasm of rectum", "Malignant Neoplasm of Rectum", "malignant neoplasm of rectum", "malignant tumor of the rectum", "Malignant Tumor of the Rectum", "Malignant Neoplasm of the Rectum", "malignant neoplasm of the rectum", "malignant neosplasm of the rectum", "Malignant tumor of rectum (disorder)", "malignant neoplasm of rectum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rectal cancer", "shortest_name_length": 13}
{"curie": "MONDO:0005716", "names": ["Contagious Pleuropneumonia", "contagious pleuropneumonia", "Contagious Pleuropneumonias", "Pleuropneumonia, Contagious", "Pleuropneumonias, Contagious"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "contagious pleuropneumonia", "shortest_name_length": 26}
{"curie": "MONDO:0012466", "names": ["PARK13", "Parkinson disease 13", "Parkinson Disease 13", "HTRA2 young-onset Parkinson disease", "susceptibility to autosomal dominant Parkinson disease 13", "young-onset Parkinson disease caused by mutation in HTRA2", "Parkinson disease 13, autosomal dominant, susceptibility to", "PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parkinson disease 13, autosomal dominant, susceptibility to", "shortest_name_length": 6}
{"curie": "UMLS:C0280349", "names": ["Stage II Lip Basal Cell Cancer", "Stage II Lip Basal Cell Carcinoma", "lip basal cell carcinoma, stage II", "Stage II Basal Cell Carcinoma of Lip", "stage II basal cell carcinoma of the lip", "Stage II Basal Cell Carcinoma of the Lip", "basal cell carcinoma of the lip, stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Lip Basal Cell Carcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0014754", "names": ["COQ10D8", "COQ7 coenzyme Q10 deficiency", "primary coenzyme Q10 deficiency 8", "COENZYME Q10 DEFICIENCY, PRIMARY, 8", "coenzyme Q10 deficiency, primary, 8", "coenzyme Q10 deficiency, primary, type 8", "coenzyme Q10 deficiency caused by mutation in COQ7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary coenzyme Q10 deficiency 8", "shortest_name_length": 7}
{"curie": "UMLS:C0751515", "names": ["Post-Traumatic Myelopathy", "Post Traumatic Myelopathy", "Myelopathy, Post-Traumatic", "Post-Traumatic Myelopathies", "Myelopathies, Post-Traumatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post-Traumatic Myelopathy", "shortest_name_length": 25}
{"curie": "MONDO:0007996", "names": ["MCOPCR", "Microphthalmia And Corectopia", "MICROPHTHALMIA AND CORECTOPIA", "microphthalmia and corectopia", "MICROPHTHALMIA, ISOLATED, WITH CORECTOPIA", "microphthalmia, isolated, with corectopia", "microphthalmia with myopia and corectopia", "Microphthalmia, Isolated, With Corectopia", "MICROPHTHALMIA WITH MYOPIA AND CORECTOPIA", "Microphthalmia With Myopia And Corectopia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microphthalmia, isolated, with corectopia", "shortest_name_length": 6}
{"curie": "UMLS:C0748538", "names": ["Scleral pigmentation", "SCLERAL PIGMENTATION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Scleral pigmentation", "shortest_name_length": 20}
{"curie": "UMLS:C1710114", "names": ["Undifferentiated Small Intestinal Cancer", "Small Intestinal Undifferentiated Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Intestinal Undifferentiated Carcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0016425", "names": ["Hughes-Stovin syndrome", "Hughes Stovin syndrome", "Hughes Stovin syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hughes-Stovin syndrome", "shortest_name_length": 22}
{"curie": "MONDO:0006889", "names": ["PARAPHIMOSIS", "paraphimosis", "Paraphimosis", "Paraphimoses", "SPANISH COLLAR", "Paraphimosis (disorder)", "paraphimosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paraphimosis", "shortest_name_length": 12}
{"curie": "MONDO:0016147", "names": ["dystrophinopathy", "qualitative or quantitative defects of dystrophin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of dystrophin", "shortest_name_length": 16}
{"curie": "MONDO:0003189", "names": ["middle ear adenocarcinoma", "middle Ear adenocarcinoma", "Middle Ear Adenocarcinoma", "Adenocarcinoma of Middle Ear", "adenocarcinoma of middle ear", "adenocarcinoma of middle Ear", "adenocarcinoma of the middle Ear", "adenocarcinoma of the middle ear", "Adenocarcinoma of the Middle Ear", "adenocarcinoma of middle ear (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "middle ear adenocarcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0022648", "names": ["cardiomyopathy and deafness due to MTTK gene mutation", "cardiomyopathy and deafness due to tRNA lysine gene mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiomyopathy and deafness due to tRNA lysine gene mutation", "shortest_name_length": 53}
{"curie": "UMLS:C3897069", "names": ["Childhood Malignant Small Intestinal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Malignant Small Intestinal Neoplasm", "shortest_name_length": 45}
{"curie": "MONDO:0018314", "names": ["infantile-onset mesial temporal lobe epilepsy with severe cognitive regression"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile-onset mesial temporal lobe epilepsy with severe cognitive regression", "shortest_name_length": 78}
{"curie": "MONDO:0010339", "names": ["EPILX1", "BATHING EPILEPSY, X-LINKED", "EPILEPSY, X-LINKED, WITH REFLEX BATHING SEIZURES", "X-linked epilepsy-learning disabilities-behavior disorders syndrome", "X-linked epilepsy with variable learning disabilities and behavior disorders", "Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders", "epilepsy, X-linked, with variable learning disabilities and behavior disorders", "epilepsy, X-linked 1, with variable learning disabilities and behavior disorders", "EPILEPSY, X-LINKED 1, WITH VARIABLE LEARNING DISABILITIES AND BEHAVIOR DISORDERS", "epilepsy, X-linked, with variable learning disabilities and behavior disorders, X-linked recessive, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, X-linked 1, with variable learning disabilities and behavior disorders", "shortest_name_length": 6}
{"curie": "MONDO:0032575", "names": ["DIAR9", "DIARRHEA 9", "diarrhea 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diarrhea 9", "shortest_name_length": 5}
{"curie": "MONDO:0500000", "names": ["EAE", "Gleich syndrome", "Gleich's syndrome", "episodic angioedema with eosinophilia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "episodic angioedema with eosinophilia", "shortest_name_length": 3}
{"curie": "MONDO:0003737", "names": ["Malignant Testicular Leydig Cell Tumor", "malignant testicular Leydig cell tumor", "testicular Leydig cell tumor, malignant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant testicular Leydig cell tumor", "shortest_name_length": 38}
{"curie": "UMLS:C0333286", "names": ["Splinter bleeding", "Splinter hemorrhage", "splinter hemorrhage", "Splinter hemorrhages", "splinter haemorrhage", "Splinter haemorrhage", "splinter hemorrhages", "SPLINTER HEMORRHAGES", "Hemorrhage, splinter", "Splinter haemorrhages", "SPLINTER HAEMORRHAGES", "splinter haemorrhages", "Splinter hemorrhage (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Splinter hemorrhage", "shortest_name_length": 17}
{"curie": "MONDO:0017690", "names": ["Galactose metabolism disorder", "metabolic disorder; galactose", "galactose; metabolic disorder", "galactose metabolism disorder", "disorder of galactose metabolism", "Disorder of galactose metabolism", "Disorders of galactose metabolism", "galactose metabolism disorder (diagnosis)", "Disorder of galactose metabolism (disorder)", "Disorders of galactose metabolism, unspecified", "carbohydrate transport and metabolism disorder galactose"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of galactose metabolism", "shortest_name_length": 29}
{"curie": "UMLS:C0852361", "names": ["skin hemorrhage", "hemorrhage skin", "Skin hemorrhage", "Skin haemorrhage", "skin hemorrhages", "hemorrhage; skin", "Skin hemorrhages", "hemorrhages skin", "skin; hemorrhage", "Skin haemorrhages", "hemorrhage; cutaneous", "cutaneous; hemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin hemorrhages", "shortest_name_length": 15}
{"curie": "MONDO:0010808", "names": ["FFI", "Fatal familial insomnia", "Familial Fatal Insomnia", "Insomnia Familial Fatal", "familial fatal insomnia", "fatal familial INSOMNIA", "Familial fatal insomnia", "FATAL FAMILIAL INSOMNIA", "fatal familial insomnia", "Insomnia familial fatal", "insomnia fatal familial", "Fatal Familial Insomnia", "INSOMNIA, FATAL FAMILIAL", "Fatal Familial Insomnias", "Familial Fatal Insomnias", "Insomnia, fatal familial", "Insomnia, Fatal Familial", "Insomnia, Familial Fatal", "Fatal Insomnia, Familial", "Fatal, Insomnia Familial", "Insomnia Familial Fatals", "Familial Fatal, Insomnia", "Fatals, Insomnia Familial", "Fatal Insomnias, Familial", "Insomnias, Familial Fatal", "Familial Fatals, Insomnia", "Insomnias, Fatal Familial", "FFI - Familial fatal insomnia", "Fatal familial insomnia (disorder)", "fatal familial insomnia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fatal familial insomnia", "shortest_name_length": 3}
{"curie": "UMLS:C4330697", "names": ["UCP2 Hyperinsulinism", "Mitochondrial Uncoupling Protein 2 Hyperinsulinism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mitochondrial Uncoupling Protein 2 Hyperinsulinism", "shortest_name_length": 20}
{"curie": "MONDO:0008849", "names": ["ava", "AVA", "Acne vermoulante", "HONEYCOMB ATROPHY", "honeycomb atrophy", "Honeycomb atrophy", "ATROPHODERMA VERMICULATA", "Atrophoderma vermiculata", "Atrophodermia reticulata", "Vermiculata atrophoderma", "atrophoderma vermiculata", "atrophoderma; vermiculate", "Atrophoderma vermiculatum", "Atrophodermia vermiculata", "ATROPHODERMIA VERMICULATA", "Honeycomb atrophy of face", "vermiculate; atrophoderma", "atrophoderma vermiculatum", "folliculitis ulerythematosa", "Atrophoderma vermiculatum (disorder)", "atrophoderma vermiculata (diagnosis)", "FOLLICULITIS ULERYTHEMATOSA RETICULATA", "Folliculitis ulerythematosa reticulata", "folliculitis ulerythematosa reticulata", "folliculitis ulerythematosa reticulate", "Folliculitis ulerythematosa reticulate", "ulerythematosa reticulata; folliculitis", "folliculitis; ulerythematosa reticulata", "Atrophodermia reticulata symmetrica faciei", "ATROPHODERMIA RETICULATA SYMMETRICA FACIEI", "Atrophodermia Reticulata Symmetrica Faciei"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrophoderma vermiculata", "shortest_name_length": 3}
{"curie": "MONDO:0005300", "names": ["CRF", "CKD", "crf", "ESRD", "esrd", "Chronic renal failure", "Chronic renal disease", "Chronic Renal Failure", "Failure;renal;chronic", "Chronic Renal Disease", "renal disease chronic", "CHRONIC RENAL FAILURE", "chronic disease renal", "Renal failure chronic", "RENAL FAILURE CHRONIC", "RENAL DISEASE CHRONIC", "chronic renal disease", "chronic renal failure", "Chronic_Renal_Disease", "Chronic Kidney Disease", "Kidney failure chronic", "chronic kidney failure", "Renal Disease, Chronic", "RENAL FAILURE, CHRONIC", "chronic diseases renal", "Disease, Chronic Renal", "Loss of renal function", "Chronic Kidney Failure", "chronic kidney disease", "Renal failure, chronic", "Chronic kidney disease", "KIDNEY FAILURE CHRONIC", "Chronic Renal Diseases", "Chronic kidney failure", "Renal Failure, Chronic", "Disease, Chronic Kidney", "End-stage renal failure", "end-stage renal disease", "End-Stage Renal Failure", "RENAL DISEASE END STAGE", "End-stage renal disease", "End-Stage Renal Disease", "Renal Diseases, Chronic", "kidney disease, chronic", "End stage renal disease", "Chronic Kidney Diseases", "end stage renal disease", "renal failure - chronic", "Kidney Failure, Chronic", "End stage renal failure", "Kidney Disease, Chronic", "End Stage Renal Disease", "end-stage renal failure", "end stage renal failure", "Diseases, Chronic Renal", "Renal Disease, End-Stage", "end-stage kidney disease", "End-Stage Kidney Disease", "KIDNEY, FAILURE, CHRONIC", "Diseases, Chronic Kidney", "Renal Disease, End Stage", "End stage kidney disease", "Kidney Diseases, Chronic", "kidney; disease, chronic", "Disease, End-Stage Renal", "End Stage Kidney Disease", "Renal Failure, End Stage", "Renal Failure, End-Stage", "End-stage kidney disease", "end stage kidney disease", "Disease, End-Stage Kidney", "RENAL FAILURE PROGRESSIVE", "Progressive renal failure", "Kidney Disease, End-Stage", "Chronic renal failure NOS", "Renal failure, progressive", "Chronic Renal Insufficiency", "chronic renal insufficiency", "CRF - Chronic Renal Failure", "CRF - Chronic renal failure", "Chronic renal insufficiency", "chronic renal failure (CRF)", "RENAL FAILURE CHRONIC UREMIA", "Chronic kidney disease (CKD)", "CKD - Chronic Kidney Disease", "CKD - chronic kidney disease", "end stage renal disease (ESRD)", "ESRF - End stage renal failure", "ESRD (end stage renal disease)", "Chronic renal failure syndrome", "End stage renal disease (ESRD)", "ESRD - End stage renal disease", "chronic renal failure syndrome", "RENAL FAILURE CHRONIC <UREMIA>", "End stage chronic renal failure", "RENAL INSUFFICIENCY PROGRESSIVE", "Progressive renal insufficiency", "Renal insufficiency, progressive", "Chronic kidney disease (disorder)", "chronic renal failure (diagnosis)", "Unspecified chronic renal failure", "End-stage renal disease (disorder)", "Chronic renal failure, unspecified", "end stage renal disease (diagnosis)", "Chronic kidney disease, unspecified", "Chronic renal failure syndrome, NOS", "disease (or disorder); kidney, chronic", "ESCRF - End stage chronic renal failure", "disease (or disorder); renal, end-stage", "disease (or disorder); kidney, end-stage", "Chronic renal failure syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic kidney disease", "shortest_name_length": 3}
{"curie": "UMLS:C4744557", "names": ["Metastatic Oral Cavity Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Oral Cavity Carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0000807", "names": ["latex allergy", "Latex allergy", "Latex Allergy", "Allergy, Latex", "rubber allergy", "Rubber Allergy", "Allergy, Rubber", "latex allergies", "Latex Allergies", "Rubber Allergies", "Allergy to latex", "allergy to latex", "Allergies, Latex", "rubber allergies", "Allergies, Rubber", "latex sensitivity", "Rubber Latex Allergy", "Allergy, Rubber Latex", "latex hypersensitivity", "Latex Hypersensitivity", "Rubber Latex Allergies", "Allergies, Rubber Latex", "Hypersensitivity, Latex", "Latex Hypersensitivities", "Hypersensitivities, Latex", "Natural Rubber Latex Allergy", "Allergy to Hevea brasiliensis latex protein", "Allergy to Hevea brasiliensis latex protein (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "latex allergy", "shortest_name_length": 13}
{"curie": "MONDO:0007030", "names": ["Aarskog syndrome", "Aarskog-Scott syndrome", "faciogenital dysplasia", "autosomal dominant Aarskog syndrome", "Aarskog syndrome, autosomal dominant", "AARSKOG SYNDROME, AUTOSOMAL DOMINANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant Aarskog syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0017731", "names": ["glycoproteinosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycoproteinosis", "shortest_name_length": 16}
{"curie": "UMLS:C0854885", "names": ["Pericardial mesothelioma malignant recurrent", "Recurrent Pericardial Malignant Mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pericardial mesothelioma malignant recurrent", "shortest_name_length": 44}
{"curie": "UMLS:C0426747", "names": ["anal bleed", "anus bleed", "bleeding anus", "anus bleeding", "Anal bleeding", "anal bleeding", "bleeding anal", "ANAL BLEEDING", "Anal Hemorrhage", "anal hemorrhage", "Anal hemorrhage", "anus; hemorrhage", "hemorrhage; anus", "Anal haemorrhage", "Hemorrhage of anus", "bleeding from anus", "Bleeding from anus", "Haemorrhage of anus", "anal hemorrhage (diagnosis)", "Bleeding from anus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bleeding from anus", "shortest_name_length": 10}
{"curie": "MONDO:0019028", "names": ["amoebiasis due to Entamoeba histolytica", "Amoebiasis due to Entamoeba histolytica"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amoebiasis due to Entamoeba histolytica", "shortest_name_length": 39}
{"curie": "MONDO:0013597", "names": ["BDPLT14", "thromboxane synthase deficiency", "THROMBOXANE SYNTHETASE DEFICIENCY", "Thromboxane Synthetase Deficiency", "Thromboxane synthetase deficiency", "thromboxane synthetase deficiency", "platelet-type bleeding disorder 14", "bleeding disorder, platelet-type, 14", "BLEEDING DISORDER, PLATELET-TYPE, 14", "Thromboxane synthetase deficiency (disorder)", "TBXAS1 inherited bleeding disorder, platelet-type", "inherited bleeding disorder, platelet-type caused by mutation in TBXAS1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "platelet-type bleeding disorder 14", "shortest_name_length": 7}
{"curie": "UMLS:C0281839", "names": ["rupture esophagus", "esophagus rupture", "Esophageal rupture", "esophageal rupture", "esophagus; rupture", "rupture; esophagus", "Esophageal Rupture", "ESOPHAGUS, RUPTURE", "Oesophageal rupture", "oesophageal rupture", "Rupture of esophagus", "rupture of esophagus", "Rupture of oesophagus", "Disruption of esophagus", "Disruption of oesophagus", "Bursting injury of esophagus", "Bursting injury of oesophagus", "Rupture of esophagus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rupture of esophagus", "shortest_name_length": 17}
{"curie": "MONDO:0002886", "names": ["common bile duct disease", "Common Bile Duct Diseases", "common bile duct disorder", "disease of common bile duct", "disorder of common bile duct", "common bile duct disease or disorder", "disease or disorder of common bile duct"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "common bile duct disorder", "shortest_name_length": 24}
{"curie": "MONDO:0001893", "names": ["spinal cord melanoma", "Spinal Cord Melanoma", "melanoma of spinal cord", "Melanoma of Spinal Cord", "melanoma of the Spinal Cord", "melanoma of the spinal cord", "Melanoma of the Spinal Cord", "spinal cord melanoma (disease)", "melanoma (disease) of spinal cord"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal cord melanoma", "shortest_name_length": 20}
{"curie": "UMLS:C3900104", "names": ["Epithelioid Hemangioendothelioma", "Adult Epithelioid Hemangioendothelioma", "adult epithelioid hemangioendothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Epithelioid Hemangioendothelioma", "shortest_name_length": 32}
{"curie": "MONDO:0006111", "names": ["Urothelial Carcinoma In Situ", "Bladder Flat Intraepithelial Lesion", "bladder flat intraepithelial lesion", "Bladder Urothelial Carcinoma In Situ", "Flat Intraepithelial Lesion of the Bladder", "flat intraepithelial lesion of the bladder", "Urinary Bladder Flat Intraepithelial Lesion", "urinary bladder flat intraepithelial lesion", "Flat Intraepithelial Lesion of the Urinary Bladder", "flat intraepithelial lesion of the urinary bladder", "Flat Intraepithelial Lesion of the urinary bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder flat intraepithelial lesion", "shortest_name_length": 28}
{"curie": "MONDO:0014044", "names": ["Tyshchenko syndrome", "TYSHCHENKO SYNDROME", "TYSHCHENKO syndrome", "Dysmorphism-conductive hearing loss-heart defect syndrome", "dysmorphism-conductive hearing loss-heart defect syndrome", "Dysmorphism, conductive hearing loss, heart defect syndrome", "Facial dysmorphism, conductive hearing loss, heart defect syndrome", "Facial dysmorphism, conductive hearing loss, heart defect syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dysmorphism-conductive hearing loss-heart defect syndrome", "shortest_name_length": 19}
{"curie": "UMLS:C1333793", "names": ["Gastric Tubulovillous Adenoma", "tubulovillous adenoma of stomach", "Tubulovillous Adenoma of Stomach", "Tubulovillous Adenoma of the Stomach", "benign gastric tubulovillous adenoma", "tubulovillous adenoma of stomach (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tubulovillous adenoma of stomach", "shortest_name_length": 29}
{"curie": "MONDO:0015573", "names": ["subacute cutaneous lupus erythematosus", "Subacute Cutaneous Lupus Erythematosus", "Subacute cutaneous lupus erythematosus", "Lupus Erythematosus, Subacute Cutaneous", "Lupus Erythematosus, Cutaneous, Subacute", "lupus; erythematosus, subacute cutaneous", "SCLE - Subacute cutaneous lupus erythematosus", "SACLE - Subacute cutaneous lupus erythematosus", "Subacute cutaneous lupus erythematosus (disorder)", "subacute cutaneous lupus erythematosus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subacute cutaneous lupus erythematosus", "shortest_name_length": 38}
{"curie": "MONDO:0017577", "names": ["Shapiro syndrome", "Shapiro's syndrome", "spontaneous periodic hypothermia", "Episodic spontaneous hypothermia", "Spontaneous periodic hypothermia", "episodic spontaneous hypothermia", "spontaneous periodic hypothermia syndrome", "spontaneous recurrent hypothermia syndrome", "recurrent spontaneous hypothermia with hypoplasia of the corpus callosum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spontaneous periodic hypothermia", "shortest_name_length": 16}
{"curie": "UMLS:C5447646", "names": ["Metastatic Lung Carcinoid Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Lung Carcinoid Tumor", "shortest_name_length": 31}
{"curie": "UMLS:C0750988", "names": ["Common Carotid Artery Thrombosis", "Thrombosis, Common Carotid Artery"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Common Carotid Artery Thrombosis", "shortest_name_length": 32}
{"curie": "MONDO:0013550", "names": ["MPD4", "distal myopathy 4", "MYOPATHY, DISTAL, 4", "myopathy, distal, 4", "Williams distal myopathy", "myopathy, distal, type 4", "WILLIAMS DISTAL MYOPATHY", "distal ABD-filaminopathy", "Distal ABD-filaminopathy", "distal muscular dystrophy 4", "distal myopathy with posterior leg and anterior hand involvement", "Distal myopathy with posterior leg and anterior hand involvement", "Distal myopathy with posterior leg and anterior hand involvement (disorder)", "Distal myopathy with posterior leg and anterior hand involvement (diagnosis)", "progressive muscular dystrophy with posterior leg and anterior hand involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal myopathy with posterior leg and anterior hand involvement", "shortest_name_length": 4}
{"curie": "MONDO:0014983", "names": ["CMS21", "congenital myasthenic syndrome 21", "congenital myasthenic syndrome type 21", "SLC18A3 congenital myasthenic syndrome", "congenital myasthenic syndrome 21, presynaptic", "myasthenic syndrome, congenital, 21, presynaptic", "MYASTHENIC SYNDROME, CONGENITAL, 21, PRESYNAPTIC", "congenital myasthenic syndrome caused by mutation in SLC18A3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myasthenic syndrome 21", "shortest_name_length": 5}
{"curie": "MONDO:0010779", "names": ["isolated mitochondrial neurosensory deafness", "isolated mitochondrial sensorineural deafness", "mitochondrial nonsyndromic sensorineural deafness", "mitochondrial non-syndromic neurosensory deafness", "mitochondrial non-syndromic sensorineural deafness", "deafness, nonsyndromic sensorineural, mitochondrial", "DEAFNESS, NONSYNDROMIC SENSORINEURAL, MITOCHONDRIAL", "Deafness, nonsyndromic sensorineural, mitochondrial", "deafness, isolated, due to mitochondrial transmission", "mitochondrial non-syndromic sensorineural hearing loss"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial non-syndromic sensorineural hearing loss", "shortest_name_length": 44}
{"curie": "UMLS:C0862640", "names": ["Stage I Prostate Adenocarcinoma", "Adenocarcinoma of the prostate stage I", "Stage I Prostate Adenocarcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma of the prostate stage I", "shortest_name_length": 31}
{"curie": "MONDO:0030020", "names": ["COXPD44", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 44", "combined oxidative phosphorylation deficiency 44"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation deficiency 44", "shortest_name_length": 7}
{"curie": "MONDO:0021334", "names": ["Immunoproliferative disease", "immunoproliferative disease", "Immunoproliferative Disorder", "Immunoproliferative Diseases", "Immunoproliferative disorder", "immunoproliferative; disease", "immunoproliferative disorder", "IMMUNOPROLIFERATIVE DISEASES", "Immunoproliferative Disorders", "Disorder, Immunoproliferative", "Disorders, Immunoproliferative", "Immunoproliferative disease NOS", "Immunoproliferative disease, NOS", "Immunoproliferative disorder (disorder)", "disease (or disorder); immunoproliferative", "Immunoproliferative disease (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunoproliferative disorder", "shortest_name_length": 27}
{"curie": "MONDO:0011668", "names": ["MODY6", "MODY type 6", "MODY, type 6", "MODY, TYPE 6", "MODY, Type 6", "MODY NEUROD1 related", "diabetes mellitus MODY type 6", "NEUROD1-associated monogenic diabetes", "NEUROD1-Associated Monogenic Diabetes", "maturity-onset diabetes of the young 6", "maturity-onset diabetes of the young type 6", "type 6 maturity-onset diabetes of the young", "maturity-onset diabetes of the young, type 6", "Maturity-onset diabetes of the young, type 6", "Maturity Onset Diabetes of the Young, Type 6", "Maturity-Onset Diabetes of the Young, Type 6", "MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 6", "maturity onset diabetes of the Young, type 6", "maturity-onset diabetes of the young - type 6", "NEUROD1 maturity-onset diabetes of the young (disease)", "Maturity-onset diabetes of the young, type 6 (disorder)", "MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 6 (disorder)", "maturity-onset diabetes of the young - type 6 (diagnosis)", "Neurogenic Differentiation Factor 1-Associated Monogenic Diabetes", "neurogenic differentiation Factor 1-associated monogenic diabetes", "maturity-onset diabetes of the young (disease) caused by mutation in NEUROD1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maturity-onset diabetes of the young type 6", "shortest_name_length": 5}
{"curie": "UMLS:C1882233", "names": ["Overlap Necrotizing Arteritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Overlap Necrotizing Arteritis", "shortest_name_length": 29}
{"curie": "UMLS:C4721649", "names": ["Stage II Esophageal Squamous Cell Cancer", "Stage II Esophagus Squamous Cell Carcinoma", "Esophageal Squamous Cell Carcinoma Stage II", "Stage II Esophageal Squamous Cell Carcinoma", "Oesophageal Squamous Cell Carcinoma Stage II", "Stage II Squamous Cell Carcinoma of Esophagus", "Stage II Squamous Cell Carcinoma of the Esophagus", "Stage II Esophageal Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Esophageal Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 40}
{"curie": "UMLS:C4763786", "names": ["Refractory Primary Bone Lymphoma", "Refractory Primary Lymphoma of Bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Primary Bone Lymphoma", "shortest_name_length": 32}
{"curie": "UMLS:C1336741", "names": ["Thrombohemorrhagic Event", "thrombohemorrhagic event"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thrombohemorrhagic Event", "shortest_name_length": 24}
{"curie": "MONDO:0010005", "names": ["SACCHAROPINURIA", "saccharopinuria", "Saccharopinuria", "hyperlysinemia type II", "hyperlysinemia, type 2", "Hyperlysinemia type II", "Hyperlysinemia, type II", "HYPERLYSINEMIA, TYPE II", "Saccharopinuria (disorder)", "saccharopinuria (diagnosis)", "SACCHAROPINE DEHYDROGENASE DEFICIENCY", "saccharopine dehydrogenase deficiency", "Saccharopine dehydrogenase deficiency", "Saccharopine Dehydrogenase Deficiency Disease", "Deficiency Disease, Saccharopine Dehydrogenase", "Alpha-aminoadipic semialdehyde synthase deficiency", "ALPHA-AMINOADIPIC SEMIALDEHYDE SYNTHASE DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "saccharopinuria", "shortest_name_length": 15}
{"curie": "UMLS:C1720887", "names": ["Female Urogenital Disease", "Female Urogenital Diseases", "Urogenital Disease, Female", "Urogenital Diseases, Female", "Female Genitourinary Disease", "Genitourinary Disease, Female", "Female Genitourinary Diseases", "Genitourinary Diseases, Female"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Female Urogenital Diseases", "shortest_name_length": 25}
{"curie": "MONDO:0000743", "names": ["Hairy leukoplakia", "Hairy leucoplakia", "hairy leucoplakia", "Hairy Leukoplakia", "hairy leukoplakia", "Hairy Leukoplakias", "hairy; leukoplakia", "leukoplakia; hairy", "Leukoplakia, Hairy", "Leukoplakias, Hairy", "oral hairy keratosis", "Oral Hairy Keratosis", "Hairy oral leukoplakia", "hairy oral leukoplakia", "Oral Hairy Leukoplakia", "Oral hairy leukoplakia", "ORAL HAIRY LEUKOPLAKIA", "Leukoplakia oral hairy", "Oral hairy leucoplakia", "ORAL LEUKOPLAKIA HAIRY", "oral hairy leucoplakia", "oral hairy leukoplakia", "oral leukoplakia hairy", "Mouth Hairy Leukoplakia", "Oral Hairy Leukoplakias", "Leukoplakia, Oral Hairy", "Hairy Leukoplakia, Oral", "mouth hairy leukoplakia", "Hairy Leukoplakias, Oral", "Leukoplakia, Hairy, Oral", "Leukoplakias, Oral Hairy", "hairy leukoplakia of mouth", "Hairy Leukoplakia of Mouth", "hairy leukoplakia of tongue", "OHL - Oral hairy leucoplakia", "OHL - Oral hairy leukoplakia", "Oral Cavity Hairy Leukoplakia", "oral cavity hairy leukoplakia", "Hairy Leukoplakia of the Mouth", "hairy leukoplakia of the mouth", "hairy leukoplakia of oral mucosa", "Hairy Leukoplakia of Oral Mucosa", "Oral hairy leukoplakia (disorder)", "oral hairy leukoplakia (diagnosis)", "hairy leukoplakia of the oral mucosa", "Hairy Leukoplakia of the Oral Mucosa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oral hairy leukoplakia", "shortest_name_length": 17}
{"curie": "MONDO:0043172", "names": ["pfeiffer rockelein syndrome", "Pfeiffer Rockelein syndrome", "asymmetrical coronal synostosis, cutaneous syndactyly of fingers and toes, and jejunal atresia", "Asymmetrical coronal synostosis, cutaneous syndactyly of fingers and toes, and jejunal atresia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pfeiffer rockelein syndrome", "shortest_name_length": 27}
{"curie": "MONDO:0030399", "names": ["VSCN2", "VISCERAL NEUROPATHY, FAMILIAL, 2, AUTOSOMAL RECESSIVE", "visceral neuropathy, familial, 2, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "visceral neuropathy, familial, 2, autosomal recessive", "shortest_name_length": 5}
{"curie": "MONDO:0006741", "names": ["cerebromalacia", "Cerebromalacia", "Cerebromalacias", "encephalomalacia", "ENCEPHALOMALACIA", "Encephalomalacia", "Encephalomalacias", "Cerebral softening", "cerebromalacia (diagnosis)", "Encephalomalacia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephalomalacia", "shortest_name_length": 14}
{"curie": "UMLS:C1142151", "names": ["Scleromalacia", "scleromalacia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Scleromalacia", "shortest_name_length": 13}
{"curie": "MONDO:0001028", "names": ["acute periodontitis", "Acute periodontitis", "Acute Periodontitis", "acute pericementitis", "periodontitis; acute", "periodontitis, acute", "Acute pericementitis", "acute; periodontitis", "Aggressive periodontitis", "Acute periodontitis (disorder)", "acute periodontitis (diagnosis)", "acute pericementitis (diagnosis)", "Aggressive and acute periodontitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute pericementitis", "shortest_name_length": 19}
{"curie": "UMLS:C1335452", "names": ["Base of Tongue Adenoid Cystic Carcinoma", "Posterior Tongue Adenoid Cystic Carcinoma", "Adenoid Cystic Carcinoma of Base of Tongue", "Base of the Tongue Adenoid Cystic Carcinoma", "Adenoid Cystic Carcinoma of Posterior Tongue", "Adenoid Cystic Carcinoma of the Posterior Tongue", "Adenoid Cystic Carcinoma of the Base of the Tongue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Posterior Tongue Adenoid Cystic Carcinoma", "shortest_name_length": 39}
{"curie": "MONDO:0012755", "names": ["EA7", "episodic ataxia type 7", "Episodic ataxia type 7", "Episodic Ataxia, Type 7", "episodic ataxia, type 7", "EPISODIC ATAXIA, TYPE 7", "Episodic ataxia type 7 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "episodic ataxia type 7", "shortest_name_length": 3}
{"curie": "UMLS:C1334058", "names": ["HPV-Related Verrucous Carcinoma", "Human Papillomavirus-Related Verrucous Carcinoma", "Human Papilloma Virus-Related Verrucous Carcinoma", "Human Papilloma Virus Related Verrucous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Human Papillomavirus-Related Verrucous Carcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C0162668", "names": ["Megaconial Myopathy", "Megaconial myopathy", "Myopathy, Megaconial", "Megaconial Myopathies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Megaconial Myopathies", "shortest_name_length": 19}
{"curie": "MONDO:0008052", "names": ["myopathy with storage of glycoproteins and Glycosaminoglycans", "Myopathy with Storage of Glycoproteins and Glycosaminoglycans", "MYOPATHY WITH STORAGE OF GLYCOPROTEINS AND GLYCOSAMINOGLYCANS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy with storage of glycoproteins and Glycosaminoglycans", "shortest_name_length": 61}
{"curie": "MONDO:0100041", "names": ["secondary trimethylaminuria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary trimethylaminuria", "shortest_name_length": 27}
{"curie": "MONDO:0010529", "names": ["SCAX3", "Scax3", "Schmidley syndrome", "ataxia-deafness syndrome", "X-linked spinocerebellar ataxia 3", "Ataxia-deafness syndrome X-linked", "X-linked ataxia deafness syndrome", "X-linked ataxia-deafness syndrome", "ataxia-deafness syndrome X-linked", "ATAXIA-DEAFNESS SYNDROME, X-LINKED", "Spinocerebellar Ataxia, X-Linked 3", "ataxia-deafness syndrome, X-linked", "SPINOCEREBELLAR ATAXIA, X-LINKED 3", "Ataxia-deafness syndrome, X-linked", "spinocerebellar ataxia, X-linked 3", "Spinocerebellar ataxia, X-linked, 3", "X-linked ataxia-hearing loss syndrome", "X-linked spinocerebellar ataxia type 3", "spinocerebellar ataxia X-linked type 3", "spinocerebellar ataxia, X-linked type 3", "X-linked spinocerebellar ataxia type 3 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked spinocerebellar ataxia type 3", "shortest_name_length": 5}
{"curie": "UMLS:C3897537", "names": ["stage IIA rectal cancer", "Stage IIA Rectal Cancer", "Stage IIA Rectal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Rectal Cancer AJCC v7", "shortest_name_length": 23}
{"curie": "UMLS:C3273135", "names": ["Extrahepatic Bile Duct IPN with an Associated Invasive Carcinoma", "Extrahepatic Bile Duct Papillary Neoplasm with an Associated Invasive Carcinoma", "Extrahepatic Bile Duct Intraductal Papillary Neoplasm with an Associated Invasive Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extrahepatic Bile Duct Intraductal Papillary Neoplasm with an Associated Invasive Carcinoma", "shortest_name_length": 64}
{"curie": "UMLS:C2673892", "names": ["Ductal plate malformation", "Ductal Plate Malformation", "Ductal plate malformations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ductal plate malformation", "shortest_name_length": 25}
{"curie": "UMLS:C0270755", "names": ["Corticostriatal Spinal Degeneration", "Corticostriatal-Spinal Degeneration", "corticostriatal spinal degeneration", "Corticostriatal-spinal degeneration", "Corticostriatal spinal degeneration", "corticostriatal-spinal; degeneration", "Degeneration, Corticostriatal-Spinal", "Corticostriatal-Spinal Degenerations", "degeneration; corticostriatal-spinal", "Degenerations, Corticostriatal-Spinal", "Corticostriatal-spinal degeneration (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Corticostriatal-Spinal Degeneration", "shortest_name_length": 35}
{"curie": "UMLS:C4553873", "names": ["Stage I Differentiated Thyroid Gland Cancer", "Stage I Differentiated Thyroid Gland Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Differentiated Thyroid Gland Carcinoma AJCC v8", "shortest_name_length": 43}
{"curie": "MONDO:0004842", "names": ["Stomatitis", "stomatitis", "STOMATITIS", "Stomatitides", "Oromucositis", "mucositis oral", "Mucositis oral", "Stomatitis NOS", "Oromucositides", "MUCOSITIS ORAL", "Oral Mucositis", "oral mucositis", "Mucositis, Oral", "Stomatitis, NOS", "Oral Mucositides", "GINGIVOSTOMATITIS", "Gingivostomatitis", "Mucositides, Oral", "gingivostomatitis", "Gingival stomatitis", "Inflammation of mouth", "Stomatitis (disorder)", "stomatitis (diagnosis)", "mouth mucosa inflammation", "Inflammation of the mouth", "Inflammation of oral mucosa", "Gingivostomatitis (disorder)", "inflammation of mouth mucosa", "Inflammatory condition of oral mucous membrane"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stomatitis", "shortest_name_length": 10}
{"curie": "UMLS:C0750987", "names": ["Common Carotid Artery Disease", "Common Carotid Artery Diseases", "Arterial Diseases, Common Carotid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arterial Diseases, Common Carotid", "shortest_name_length": 29}
{"curie": "UMLS:C5205608", "names": ["Advanced Adrenal Gland Pheochromocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Adrenal Gland Pheochromocytoma", "shortest_name_length": 39}
{"curie": "UMLS:C1336438", "names": ["Stage IV Retinoblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Retinoblastoma", "shortest_name_length": 23}
{"curie": "MONDO:0008923", "names": ["cass", "CASS", "PPKCA2", "PPKCA Wallis type", "PPKCA, WALLIS TYPE", "Ppkca, Wallis type", "PPK-CA, Wallis type", "cataract, alopecia, sclerodactyly", "Cataract, alopecia, sclerodactyly", "cataract-alopecia-sclerodactyly syndrome", "Cataract-Alopecia-Sclerodactyly Syndrome", "Cataract-alopecia-sclerodactyly syndrome", "CATARACT-ALOPECIA-SCLERODACTYLY SYNDROME", "cataract, alopecia, sclerodactyly syndrome", "Cataract, alopecia, sclerodactyly syndrome", "palmoplantar keratoderma and congenital alopecia 2", "PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 2", "palmoplantar keratoderma and congenital alopecia type 2", "Palmoplantar keratoderma and congenital alopecia, Wallis type", "palmoplantar keratoderma and congenital alopecia, Wallis type", "Autosomal recessive palmoplantar keratoderma and congenital alopecia", "autosomal recessive palmoplantar keratoderma and congenital alopecia", "autosomal recessive palmoplantar hyperkeratosis and congenital alopecia", "Autosomal recessive palmoplantar hyperkeratosis and congenital alopecia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive palmoplantar keratoderma and congenital alopecia", "shortest_name_length": 4}
{"curie": "MONDO:0033015", "names": ["EKVP5", "ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 5", "erythrokeratodermia variabilis et progressiva 5", "erythrokeratodermia variabilis ET progressiva 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythrokeratodermia variabilis et progressiva 5", "shortest_name_length": 5}
{"curie": "UMLS:C4288755", "names": ["Metastatic Non-Squamous Non-Small Cell Lung Cancer", "Metastatic Non-Squamous Non-Small Cell Lung Carcinoma", "Metastatic Lung Non-Squamous Non-Small Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Lung Non-Squamous Non-Small Cell Carcinoma", "shortest_name_length": 50}
{"curie": "MONDO:0005774", "names": ["FARCY", "farcy", "Farcy", "Equina", "malleus", "Malleus", "Glanders", "GLANDERS", "glanders", "Maliasmus", "Farcy buds", "Farcy cords", "farcy pipes", "Farcy pipes", "Equine glanders", "farcy (diagnosis)", "Malleus (glanders)", "Glanders (disorder)", "Burkholderia mallei", "glanders (diagnosis)", "GLANDERS AND PSEUDOGLANDERS", "Burkholderia mallei infection", "glanders due to Malleomyces mallei", "glanders due to Pseudomonas mallei", "glanders due to Burkholderia mallei", "Infection due to Malleomyces mallei", "infection due to Pseudomonas mallei", "Infection due to malleomyces mallei", "glanders due to infection by mallei", "Infection due to Pseudomonas mallei", "glanders due to Actinobacillus mallei", "Burkholderia mallei infectious disease", "Infection due to Actinobacillus mallei", "Infection due to actinobacillus mallei", "Burkholderia mallei disease or disorder", "glanders due to Malleomyces mallei (diagnosis)", "glanders due to Pseudomonas mallei (diagnosis)", "Burkholderia mallei caused disease or disorder", "glanders due to infection by malleomyces mallei", "glanders due to infection by mallei (diagnosis)", "glanders due to Burkholderia mallei (diagnosis)", "glanders due to infection by Pseudomonas mallei", "glanders due to infection by Burkholderia mallei", "glanders due to Actinobacillus mallei (diagnosis)", "glanders due to infection by actinobacillus mallei"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glanders", "shortest_name_length": 5}
{"curie": "UMLS:C0024689", "names": ["Mandibular Disease", "Mandibular Diseases", "Disease, Mandibular", "Mandibular Disorders", "Diseases, Mandibular"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mandibular Diseases", "shortest_name_length": 18}
{"curie": "MONDO:0016118", "names": ["muscular glycogenosis", "glycogen storage myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular glycogenosis", "shortest_name_length": 21}
{"curie": "MONDO:0011110", "names": ["dyssegmental dysplasia and glaucoma", "dyssegmental dysplasia with glaucoma", "DYSSEGMENTAL DYSPLASIA WITH GLAUCOMA", "Dyssegmental Dysplasia with Glaucoma", "dyssegmental dysplasia-glaucoma syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyssegmental dysplasia-glaucoma syndrome", "shortest_name_length": 35}
{"curie": "MONDO:0001259", "names": ["Pituitary infarct", "pituitary infarct", "Pituitary infarction", "pituitary infarction", "Pituitary Infarction", "Pituitary infarct, NOS", "Pituitary infarction, NOS", "Pituitary Gland Infarction", "pituitary gland infarction", "Pituitary infarction (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pituitary gland infarction", "shortest_name_length": 17}
{"curie": "MONDO:0011382", "names": ["SCD", "scds", "Herrick", "sicklemia", "HbS disease", "HbS Disease", "Hb S disease", "hb s disease", "disease hb s", "Hb SC disease", "Hb-SS disease", "Hb SS disease", "drepanocytosis", "anemia; Herrick", "Drepanocythemia", "Herrick; anemia", "Drepanocythaemia", "HERRICK SYNDROME", "Herrick's anemia", "Hb-S/Hb-C disease", "Sickle cell anemia", "anemia sickle cell", "sickle-cell anemia", "Anemia sickle cell", "Sickle Cell Anemia", "SICKLE CELL ANEMIA", "Sickle-cell anemia", "anemia sickle-cell", "sickle cell anemia", "anemia; sickle-cell", "sickle-cell; anemia", "Sickle-cell anaemia", "sickle-cell disease", "Sickle Cell Anemias", "sickle cell anemias", "disease sickle cell", "Anaemia sickle cell", "Sickle Cell Disease", "Sickle cell disease", "sickle-cell anaemia", "SICKLE CELL DISEASE", "anemia cells sickle", "Anemia, Sickle Cell", "disease sickle-cell", "Anaemia;sickle cell", "sickle cell anaemia", "sickle cell disease", "ANEMIA, SICKLE CELL", "Sickle-cell disease", "anaemia cell sickle", "Sickle cell anaemia", "Hemoglobin S disease", "anemia sickle celled", "Cell Disease, Sickle", "sickle cell syndrome", "Anemias, Sickle Cell", "cell disorder sickle", "Sickle Cell Disorder", "sickle cell disorder", "cell sickle syndrome", "Hemoglobin S Disease", "cell diseases sickle", "Sickle Cell Diseases", "anemia cells sickles", "syndrome sickle cell", "Sickle cell syndrome", "cells disease sickle", "Disease, Hemoglobin S", "Cell Disorder, Sickle", "Hemoglobin S Diseases", "hemoglobin SC disease", "cell sickle syndromes", "Sickle cell disorders", "Sickle Cell Disorders", "Sickle-cell Disorders", "Cell Diseases, Sickle", "sickle-cell; disorder", "Hemoglobin SS Disease", "Sickle-cell disorders", "Hemoglobin SS disease", "Haemoglobin S disease", "Cell Disorders, Sickle", "haemoglobin SC disease", "Hemoglobin S-S disease", "Sickle-cell anemia NOS", "Sickle-cell disease NOS", "Haemoglobin S-S disease", "Sickle cell disease NOS", "Sickle-cell disorder NOS", "anemia cell disorder sickle", "SICKLE CELL HEMOLYTIC ANEMIA", "Hb-SS disease without crisis", "anemia cell disorders sickle", "sickle cell anemia (diagnosis)", "Sickle-cell anemia, unspecified", "sickle-cell; hemoglobin disease", "Sickle-cell anaemia, unspecified", "Sickle-cell disease, unspecified", "sickle cell-hemoglobin SS disease", "Sickle cell-hemoglobin SS disease", "Sickle cell-haemoglobin SS disease", "Hemoglobin S disease without crisis", "anemia hemolytic sickle cell anemia", "Sickling disorder due to hemoglobin S", "Sickling Disorder due to Hemoglobin S", "sickling disorder due to Hemoglobin S", "Sickling Disorder Due to Hemoglobin S", "anemia hemolytic sickle Hb-SS disease", "Sickling disorder due to haemoglobin S", "sickle-cell/Hb-C disease without crisis", "Sickle-cell/Hb-C disease without crisis", "Sickle cell-hemoglobin SS disease (disorder)", "sickle cell-hemoglobin SS disease (diagnosis)", "Sickling disorder due to hemoglobin S (disorder)", "Hereditary hemoglobinopathy disorder homozygous for hemoglobin S", "Hereditary haemoglobinopathy disorder homozygous for haemoglobin S"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sickle cell anemia", "shortest_name_length": 3}
{"curie": "MONDO:0024627", "names": ["defective phagocytosis", "phagocyte cell dysfunction", "Phagocytic cell dysfunction", "phagocytic cell dysfunction", "phagocyte cell dysfunction (diagnosis)", "Phagocytic cell dysfunction (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phagocytic cell dysfunction", "shortest_name_length": 22}
{"curie": "UMLS:C1336441", "names": ["Stage IV Testicular Nonseminomatous Germ Cell Tumor", "Stage IV Testicular Non-Seminomatous Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Testicular Non-Seminomatous Germ Cell Tumor", "shortest_name_length": 51}
{"curie": "MONDO:0020456", "names": ["pleuro-pericardial cyst"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pleuro-pericardial cyst", "shortest_name_length": 23}
{"curie": "UMLS:C5205727", "names": ["Prostate Synovial Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Synovial Sarcoma", "shortest_name_length": 25}
{"curie": "MONDO:0011335", "names": ["SEMDJL2", "SEMD-MD", "Spondyloepimetaphyseal Dysplasia with Joint Laxity Type 2", "spondyloepimetaphyseal dysplasia with JOINT laxity type 2", "spondyloepimetaphyseal dysplasia with joint laxity type 2", "Spondyloepimetaphyseal dysplasia with joint laxity type 2", "SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2", "spondyloepimetaphyseal dysplasia with Joint laxity, type 2", "spondyloepimetaphyseal dysplasia with JOINT laxity, type 2", "spondyloepimetaphyseal dysplasia with multiple dislocations", "Spondyloepimetaphyseal dysplasia with multiple dislocations", "Spondyloepimetaphyseal dysplasia with joint laxity Hall type", "SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, HALL TYPE", "spondyloepimetaphyseal dysplasia with Joint laxity, Hall type", "Spondyloepimetaphyseal dysplasia with joint laxicity, Hall type", "spondyloepimetaphyseal dysplasia with joint laxicity, Hall type", "Spondyloepimetaphyseal dysplasia with joint laxity leptodactylic type", "Spondyloepimetaphyseal dysplasia with multiple dislocations Hall type", "spondyloepimetaphyseal dysplasia with multiple dislocations Hall type", "spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type", "Spondyloepimetaphyseal dysplasia with multiple dislocations, Hall type", "Spondyloepimetaphyseal dysplasia with multiple dislocations, hall type", "Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type", "spondyloepimetaphyseal dysplasia with Joint laxity, leptodactylic type", "SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH MULTIPLE DISLOCATIONS, HALL TYPE", "Spondyloepimetaphyseal dysplasia with multiple dislocations (disorder)", "SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, LEPTODACTYLIC TYPE", "spondyloepimetaphyseal dysplasia with multiple dislocations, Hall type", "spondyloepimetaphyseal dysplasia with multiple dislocations (diagnosis)", "spondyloepimetaphyseal dysplasia with multiple dislocations leptodactylic type", "Spondyloepimetaphyseal dysplasia with multiple dislocations, leptodactylic type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepimetaphyseal dysplasia with multiple dislocations", "shortest_name_length": 7}
{"curie": "MONDO:0030008", "names": ["COXPD42", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 42", "combined oxidative phosphorylation deficiency 42"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation deficiency 42", "shortest_name_length": 7}
{"curie": "MONDO:0022863", "names": ["corneal crystals myopathy neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal crystals myopathy neuropathy", "shortest_name_length": 36}
{"curie": "MONDO:0033562", "names": ["NEDDISH", "neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia", "NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, IMPAIRED SPEECH, AND HYPOTONIA", "neurodevelopmental disorder with dysmorphic facies, impaired speech, and hypotonia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with dysmorphic facies, impaired speech, and hypotonia", "shortest_name_length": 7}
{"curie": "MONDO:0018988", "names": ["ICE Syndrome", "ICE syndrome", "Chandler's (PA) syndrome", "Irido-corneo-endothelial syndrome", "iridocorneal endothelial syndrome", "Iridocorneal endothelial syndrome", "Iridocorneal Endothelial Syndrome", "Iridocorneal Endothelial Syndromes", "Endothelial Syndrome, Iridocorneal", "ICE - Iridocorneal endothelial syndrome", "ICE - Irido-corneo-endothelial syndrome", "Iridocorneal endothelial syndrome (disorder)", "ICE syndrome - Iridio-corneo-endothelial syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "iridocorneal endothelial syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0012593", "names": ["CAHTP", "BLT syndrome", "Brain-Lung-Thyroid Syndrome", "BRAIN-LUNG-THYROID SYNDROME", "Brain lung thyroid syndrome", "Brain-lung-thyroid syndrome", "brain-lung-thyroid syndrome", "brain-lung-thyroid syndrome (diagnosis)", "choreoathetosis-hypothyroidism-neonatal respiratory distress", "Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress", "choreoathetosis, hypothyroidism, and neonatal respiratory distress", "Choreoathetosis-hypothyroidism-neonatal respiratory distress syndrome", "choreoathetosis-hypothyroidism-neonatal respiratory distress syndrome", "CHOREOATHETOSIS AND CONGENITAL HYPOTHYROIDISM WITH OR WITHOUT PULMONARY DYSFUNCTION", "choreoathetosis and congenital hypothyroidism with or without pulmonary dysfunction", "Choreoathetosis with congenital hypothyroidism and neonatal respiratory distress syndrome", "Choreoathetosis with congenital hypothyroidism and neonatal respiratory distress syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brain-lung-thyroid syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0017395", "names": ["fix drug eruption", "Fixed drug eruption", "drug eruption fixed", "Fixed Drug Eruption", "fixed drug eruption", "Drug eruption, fixed", "drug eruptions fixed", "fixed drug eruptions", "drugs eruption fixed", "DRUG ERUPTIONS, FIXED", "fixed pigmented erythema", "Fixed drug eruption, NOS", "FDE - Fixed drug eruption", "Fixed drug eruption (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fixed pigmented erythema", "shortest_name_length": 17}
{"curie": "MONDO:0060733", "names": ["HHRRD", "Hfhrtrd", "HFHRTRD", "HUMEROFEMORAL HYPOPLASIA WITH RADIOTIBIAL RAY DEFICIENCY", "humerofemoral hypoplasia with radiotibial ray deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "humerofemoral hypoplasia with radiotibial ray deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0032748", "names": ["SPGF38", "SPERMATOGENIC FAILURE 38", "spermatogenic failure 38"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 38", "shortest_name_length": 6}
{"curie": "MONDO:0000060", "names": ["microcephalic osteodysplastic primordial dwarfism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephalic osteodysplastic primordial dwarfism", "shortest_name_length": 49}
{"curie": "MONDO:0018280", "names": ["MEB disease with bilateral multicystic leucodystrophy", "muscle-eye-brain disease with bilateral multicystic leucodystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscle-eye-brain disease with bilateral multicystic leucodystrophy", "shortest_name_length": 53}
{"curie": "UMLS:C5556798", "names": ["Refractory Cervical Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Cervical Adenocarcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0005515", "names": ["oral cancer", "Oral Cancer", "ORAL CANCER", "Mouth cancer", "mouth cancer", "oral cancers", "Mouth Cancer", "Oral Cancers", "Cancer, Oral", "Mouth--Cancer", "Mouth Cancers", "Cancers, Oral", "mouth cancers", "Cancer, Mouth", "Cancers, Mouth", "cancer of mouth", "Cancer of Mouth", "CA - Mouth cancer", "oral cavity cancer", "cancer of the mouth", "Cancer of the Mouth", "cancer of oral cavity", "Malignant Mouth Tumor", "Cancer of oral cavity", "malignant mouth tumor", "Oral neoplasm malignant", "Malignant Oral Neoplasm", "ORAL NEOPLASM MALIGNANT", "Malignant Tumor of Mouth", "Malignant Mouth Neoplasm", "malignant mouth neoplasm", "Malignant tumor of mouth", "malignant tumor of mouth", "Malignant tumour of mouth", "malignant neoplasm of mouth", "Malignant neoplasm of mouth", "Malignant Oral Cavity Tumor", "Malignant Neoplasm of Mouth", "malignant oral cavity tumor", "malignant tumor of the mouth", "Malignant Tumor of the Mouth", "Malignant Oral Cavity Neoplasm", "Malignant tumor of oral cavity", "malignant oral cavity neoplasm", "malignant tumor of oral cavity", "Malignant Neoplasm of the Mouth", "Malignant oral cavity neoplasms", "malignant neoplasm of the mouth", "Malignant tumour of oral cavity", "Malignant neoplasm of mouth, NOS", "malignant neoplasm of oral cavity", "malignant neoplasm of floor of mouth", "Malignant neoplasm of oral cavity NOS", "Malignant Lip and Oral Cavity Neoplasm", "Malignant neoplasm of mouth, unspecified", "Malignant tumor of lateral floor of mouth", "malignant tumor of lateral floor of mouth", "malignant tumor of the floor of the mouth", "Malignant tumor of oral cavity (disorder)", "Malignant tumor of anterior floor of mouth", "malignant tumor of anterior floor of mouth", "Malignant tumour of lateral floor of mouth", "Malignant tumour of anterior floor of mouth", "Malignant neoplasm of lateral floor of mouth", "malignant neoplasm of lateral floor of mouth", "malignant neoplasm of oral cavity (diagnosis)", "Malignant neoplasm of anterior floor of mouth", "malignant tumor of lateral portion of floor of mouth", "Malignant tumor of lateral floor of mouth (disorder)", "Malignant tumor of anterior floor of mouth (disorder)", "malignant tumor of anterior portion of floor of mouth", "Malignant neoplasm of lateral portion of floor of mouth", "malignant neoplasm of lateral portion of floor of mouth", "Malignant neoplasm of anterior portion of floor of mouth", "malignant neoplasm of anterior portion of floor of mouth", "malignant neoplasm of lateral portion of floor of mouth (diagnosis)", "malignant neoplasm of anterior portion of floor of mouth (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oral cavity cancer", "shortest_name_length": 11}
{"curie": "UMLS:C3273216", "names": ["Invasive Breast Lobular Carcinoma, Pleomorphic Variant", "Invasive Lobular Breast Carcinoma, Pleomorphic Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Invasive Breast Lobular Carcinoma, Pleomorphic Variant", "shortest_name_length": 54}
{"curie": "UMLS:C1336322", "names": ["Stage II Supradiaphragmatic Hodgkin Lymphoma", "Stage II Supradiaphragmatic Hodgkin's Disease", "Stage II Supradiaphragmatic Hodgkin's Lymphoma", "Stage II Hodgkin's Disease above the Diaphragm", "Stage II Hodgkin's Lymphoma above the Diaphragm", "Ann Arbor Stage II Supradiaphragmatic Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage II Supradiaphragmatic Hodgkin Lymphoma", "shortest_name_length": 44}
{"curie": "UMLS:C0855217", "names": ["Lack of spontaneous speech"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lack of spontaneous speech", "shortest_name_length": 26}
{"curie": "UMLS:C0752160", "names": ["Central Nervous System Cavernous Hemangioma", "Cavernous Hemangioma, Central Nervous System", "Hemangioma, Cavernous, Central Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemangioma, Cavernous, Central Nervous System", "shortest_name_length": 43}
{"curie": "MONDO:0002587", "names": ["encapsulated thymoma", "Encapsulated Thymoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encapsulated thymoma", "shortest_name_length": 20}
{"curie": "MONDO:0045033", "names": ["opportunistic systemic mycosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "opportunistic systemic mycosis", "shortest_name_length": 30}
{"curie": "UMLS:C1332201", "names": ["Diffuse Large B-Cell Lymphoma", "Adult Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Diffuse Large B-Cell Lymphoma", "shortest_name_length": 29}
{"curie": "UMLS:C1708403", "names": ["Hypothalamic Gangliocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypothalamic Gangliocytoma", "shortest_name_length": 26}
{"curie": "UMLS:C4743983", "names": ["Advanced Extremity Melanoma", "Advanced Melanoma of the Extremity", "Advanced Cutaneous Melanoma of the Extremity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Cutaneous Melanoma of the Extremity", "shortest_name_length": 27}
{"curie": "UMLS:C1336113", "names": ["stage IA endometrial cancer", "stage IA uterine corpus cancer", "Stage IA Uterine Corpus Cancer", "stage IA endometrial carcinoma", "stage IA uterine corpus cancer AJCC v7", "Stage IA Uterine Corpus Cancer AJCC v7", "Stage IA Uterine (including Endometrial) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Uterine Corpus Cancer AJCC v7", "shortest_name_length": 27}
{"curie": "MONDO:0023158", "names": ["Fitz-Hugh (etiology)", "Perihepatitis Syndrome", "perihepatitis syndrome", "Gonococcal Perihepatitis", "fitzhugh-curtis syndrome", "curtis fitzhugh syndrome", "Perihepatitis gonococcal", "Fitzhugh Curtis syndrome", "gonococcal perihepatitis", "FITZHUGH-CURTIS SYNDROME", "Gonococcal perihepatitis", "fitzhugh curtis syndrome", "fitz-hugh-curtis syndrome", "FITZ-HUGH-CURTIS SYNDROME", "Fitz-Hugh (manifestation)", "Fitz-Hugh-Curtis syndrome", "Fitz-Hugh and Curtis syndrome", "Gonococcal perihepatitis (disorder)", "gonococcal perihepatitis (diagnosis)", "Fitz-Hugh-Curtis syndrome (disorder)", "Fitz-Hugh-Curtis syndrome (diagnosis)", "Fitz-Hugh-Curtis syndrome - gonococcal", "PERITONITIS, GONOCCOCIC OF UPPER ABDOMEN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fitz-Hugh-Curtis syndrome", "shortest_name_length": 20}
{"curie": "MONDO:0001355", "names": ["siderosis; eye", "eye; siderosis", "siderosis bulbi", "Ocular siderosis", "ocular siderosis", "siderosis of eye", "Siderosis of eye", "Siderosis of globe", "siderosis of globe", "Siderosis of eye (disorder)", "ocular siderosis (diagnosis)", "camera-type eye hemosiderosis", "hemosiderosis of camera-type eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ocular siderosis", "shortest_name_length": 14}
{"curie": "UMLS:C4049248", "names": ["Rebound atopic dermatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rebound atopic dermatitis", "shortest_name_length": 25}
{"curie": "UMLS:C4055497", "names": ["ALL ROSE Cluster", "ALL Gene Expression Cluster", "Acute Lymphoblastic Leukemia ROSE Cluster", "Acute Lymphoblastic Leukemia by ROSE Cluster", "Acute Lymphoblastic Leukemia Gene Expression Cluster"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Lymphoblastic Leukemia by ROSE Cluster", "shortest_name_length": 16}
{"curie": "MONDO:0004934", "names": ["periosteum", "Periosteum", "Periostitis", "PERIOSTITIS", "periostitis", "periosteitis", "PERIOSTEITIS", "Periostalgia", "Periosteitis", "Periostitides", "Periostitis, NOS", "Periosteitis fibrosa", "periostitis (disease)", "Periostitis (disorder)", "periosteum inflammation", "periostitis (diagnosis)", "inflammation of periosteum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "periostitis", "shortest_name_length": 10}
{"curie": "UMLS:C4744483", "names": ["Recurrent Chordoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Chordoma", "shortest_name_length": 18}
{"curie": "UMLS:C0233414", "names": ["Impaired Attention", "Attention disturbances", "Disturbance of attention", "Disturbance in attention", "Disturbance of attention, NOS", "Disturbance of attention (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disturbance of attention", "shortest_name_length": 18}
{"curie": "MONDO:0010657", "names": ["MRX3", "MAHCX", "XLID3", "X-linked mental retardation 3", "Mental Retardation, X-Linked 3", "MENTAL RETARDATION, X-LINKED 3", "mental retardation, X-linked 3", "intellectual disability, X-linked 3", "X-linked mental retardation 3 (MRX3, XLMR3)", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 3", "methylmalonic acidemia and homocysteinemia cblX type", "methylmalonic acidemia and homocysteinemia type cblX", "METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblX TYPE", "Methylmalonic acidemia with homocystinuria, type cblX", "METHYLMALONIC ACIDEMIA AND HOMOCYSTEINEMIA, cblX TYPE", "methylmalonic acidemia with homocystinuria, type cblX", "methylmalonic acidemia and HOMOCYSTEINEMIA, cblX type", "methylmalonic aciduria with homocystinuria, type cblX", "Methylmalonic aciduria with homocystinuria, type cblX", "methylmalonic aciduria and homocysteinemia, cblx type, X-linked recessive", "combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblX", "Combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblX"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "methylmalonic acidemia with homocystinuria, type cblX", "shortest_name_length": 4}
{"curie": "MONDO:0010639", "names": ["Plott syndrome", "laryngeal abductor paralysis", "vocal cord dysfunction, familial", "laryngeal abductor paralysis-intellectual disability syndrome", "Laryngeal abductor paralysis-intellectual disability syndrome", "Laryngeal abductor paralysis with intellectual disability syndrome", "laryngeal abductor paralysis with intellectual disability syndrome", "Laryngeal abductor paralysis with intellectual disability syndrome (disorder)", "laryngeal abductor paralysis with intellectual disability syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laryngeal abductor paralysis-intellectual disability syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0003682", "names": ["localized chondrosarcoma", "Chondrosarcoma localised", "Chondrosarcoma localized", "Localized Chondrosarcoma", "Chondrosarcoma, Localized", "chondrosarcoma, localized"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "localized chondrosarcoma", "shortest_name_length": 24}
{"curie": "UMLS:C3639953", "names": ["CAVD, Balanced", "Complete AV Canal Defect Balanced", "Complete Atrioventricular Canal Defect Balanced", "Complete Atrioventricular Canal Defect (Balanced)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Complete Atrioventricular Canal Defect Balanced", "shortest_name_length": 14}
{"curie": "MESH:D009444", "names": ["Neuritis, Autoimmune, Experimental"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neuritis, Autoimmune, Experimental", "shortest_name_length": 34}
{"curie": "MONDO:0008329", "names": ["PHA1A", "PHA1AD", "renal PHA1", "Renal PHA1", "Autosomal dominant PHA1", "autosomal dominant PHA 1", "PHA I, autosomal dominant", "PHA I, AUTOSOMAL DOMINANT", "renal pseudohypoaldosteronism type 1", "Renal pseudohypoaldosteronism type 1", "pseudohypoaldosteronism type 1, dominant", "Autosomal dominant pseudohypoaldosteronism type 1", "pseudohypoaldosteronism type 1 autosomal dominant", "Pseudohypoaldosteronism Type I Autosomal Dominant", "autosomal dominant pseudohypoaldosteronism type 1", "Pseudohypoaldosteronism Type 1, Autosomal Dominant", "pseudohypoaldosteronism type i, autosomal dominant", "pseudohypoaldosteronism, type I, autosomal dominant", "PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL DOMINANT", "Pseudohypoaldosteronism, Type I, Autosomal Dominant", "Hyponatremic Mineralocorticoid Resistance due to Mineralocorticoid Receptor Defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant pseudohypoaldosteronism type 1", "shortest_name_length": 5}
{"curie": "MONDO:0009942", "names": ["camera syndrome", "Camera syndrome", "PYKNOACHONDROGENESIS", "pyknoachondrogenesis", "Pyknoachondrogenesis", "Pyknoachondrogenesis (disorder)", "association of skeletal defects resembling achondrogenesis with generalized bone sclerosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyknoachondrogenesis", "shortest_name_length": 15}
{"curie": "UMLS:C5557401", "names": ["Vulvar Ewing Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Ewing Sarcoma", "shortest_name_length": 20}
{"curie": "MONDO:0030608", "names": ["ILD1", "interstitial lung disease 1", "INTERSTITIAL LUNG DISEASE 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "interstitial lung disease 1", "shortest_name_length": 4}
{"curie": "MONDO:0009905", "names": ["Urban syndrome", "Urban-Rogers-Meyer syndrome", "urban-Rogers-Meyer syndrome", "Urban Rogers Meyer syndrome", "URBAN-ROGERS-MEYER SYNDROME", "Urban-Rogers-Meyer Syndrome", "PRADER-WILLI HABITUS, OSTEOPENIA, AND CAMPTODACTYLY", "Prader-Willi habitus, osteopenia, and camptodactyly", "Prader-Willi habitus-osteopenia-camptodactyly syndrome", "Prader Willi habitus with osteopenia and camptodactyly", "Prader-Willi habitus-osteoporosis-hand contractures syndrome", "intellectual disability-short stature-hand contractures-genital anomalies syndrome", "Intellectual disability-short stature-hand contractures-genital anomalies syndrome", "Intellectual disability and short stature with hand contracture and genital anomaly syndrome", "Intellectual disability and short stature with hand contracture and genital anomaly syndrome (disorder)", "Intellectual disability and short stature with hand contracture and genital anomaly syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urban-Rogers-Meyer syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C0278780", "names": ["relapsed adult AML", "Relapsed Adult AML", "Recurrent Adult AML", "relapsed adult ANLL", "recurrent adult AML", "adult AML, relapsed", "adult AML, recurrent", "AML, adult recurrent", "AML, relapsed, adult", "recurrent adult ANLL", "ANLL, adult recurrent", "ANLL, relapsed, adult", "adult ANLL, recurrent", "Relapsed Adult Acute Myeloid Leukemia", "relapsed adult acute myeloid leukemia", "myeloid leukemia, relapsed adult acute", "adult leukemia, relapsed acute myeloid", "Recurrent Acute Myeloid Leukemia (AML)", "leukemia, relapsed adult acute myeloid", "adult acute myeloid leukemia, relapsed", "recurrent adult acute myeloid leukemia", "Recurrent Adult Acute Myeloid Leukemia", "recurrent acute myeloid leukemia, adult", "acute myeloid leukemia, relapsed, adult", "relapsed adult acute myelogenous leukemia", "Relapsed Adult Acute Myelogenous Leukemia", "Recurrent Adult Acute Myelogenous Leukemia", "adult leukemia, relapsed acute myelogenous", "myelogenous leukemia, relapsed adult acute", "adult acute myelogenous leukemia, relapsed", "leukemia, relapsed adult acute myelogenous", "acute myelogenous leukemia, relapsed, adult", "leukemia, relapsed adult acute nonlymphocytic", "adult acute nonlymphocytic leukemia, relapsed", "nonlymphocytic leukemia, relapsed adult acute", "adult leukemia, relapsed acute nonlymphocytic", "Recurrent Adult Acute Non-Lymphocytic Leukemia", "acute nonlymphocytic leukemia, relapsed, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "recurrent adult acute myeloid leukemia", "shortest_name_length": 18}
{"curie": "UMLS:C4724714", "names": ["Langerhans Cell Histiocytosis, Disseminated", "Langerhans cell histiocytosis, disseminated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Langerhans Cell Histiocytosis, Disseminated", "shortest_name_length": 43}
{"curie": "UMLS:C0343113", "names": ["Senile Nevus", "Senile nevus", "Senile naevus", "senile; nevus", "nevus; senile", "Nevus, senile", "Senile nevus (disorder)", "non-neoplastic senile nevus", "non-neoplastic senile nevus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Senile nevus", "shortest_name_length": 12}
{"curie": "MONDO:0017521", "names": ["hyperphalangy, unilateral", "hyperphalangy in digits 2-5", "supernumerary phalanx, unilateral", "supernumerary phalanges, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperphalangy, unilateral", "shortest_name_length": 25}
{"curie": "MONDO:0008167", "names": ["Dermoid cyst", "teratoma, ovarian", "Teratoma, Ovarian", "cyst dermoid ovary", "dermoid cyst ovary", "ovary dermoid cyst", "cysts dermoid ovary", "ovary; cyst, dermoid", "dermoid ovarian cyst", "ovarian cyst dermoid", "cyst dermoid ovaries", "ovarian dermoid cyst", "Ovarian dermoid cyst", "Ovarian Dermoid Cyst", "OVARIAN CYST DERMOID", "cysts dermoid ovarian", "dermoid cyst, ovarian", "Dermoid Cyst of Ovary", "cyst dermoid of ovary", "Dermoid Cyst, Ovarian", "cysts dermoid ovaries", "dermoid cyst of ovary", "Dermoid cyst of ovary", "DERMOID CYST, OVARIAN", "Dermoid Cyst of the Ovary", "dermoid cyst of the ovary", "dermoid cyst (& [ovarian])", "benign dermoid cyst of ovary", "cyst; ovary, ovarian, dermoid", "Mature cystic ovarian teratoma", "Mature cystic teratoma of ovary", "benign dermoid cyst of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermoid cyst of ovary", "shortest_name_length": 12}
{"curie": "UMLS:C0276684", "names": ["Thrush balanitis", "Balanitis candida", "candida balanitis", "Candida balanitis", "BALANITIS CANDIDA", "Candidal balanitis", "Monilial balanitis", "candidal balanitis", "Balanitis monilial", "Candidal balanitis (disorder)", "candidal balanitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Candidal balanitis", "shortest_name_length": 16}
{"curie": "MONDO:0002865", "names": ["Anal Sarcoma", "anal sarcoma", "anus sarcoma", "Sarcoma of Anus", "sarcoma of anus", "sarcoma of the anus", "Sarcoma of the Anus", "sarcoma of anus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anus sarcoma", "shortest_name_length": 12}
{"curie": "UMLS:C1112258", "names": ["driving phobia", "phobia driving", "phobia of driving", "Phobia of Driving", "Phobia of driving"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Phobia of driving", "shortest_name_length": 14}
{"curie": "MONDO:0013564", "names": ["AHP", "Ahaptoglobinemia", "AHAPTOGLOBINEMIA", "ANHAPTOGLOBINEMIA", "anhaptoglobinemia", "HYPOHAPTOGLOBINEMIA", "hypohaptoglobinemia", "HYPOHAPTOGLOBINEMIA (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anhaptoglobinemia", "shortest_name_length": 3}
{"curie": "MONDO:0005397", "names": ["GOITRE", "Goitre", "Goiter", "goiter", "struma", "Struma", "goitre", "GOITER", "goiters", "Goiters", "goitres", "Goiter NOS", "Goitre, NOS", "Goiter, NOS", "Thyromegaly", "thyromegaly", "THYROMEGALY", "thyroid goiter", "Thyroid goitre", "Thyroid goiter", "THYROID GOITER", "goiter thyroid", "Struma - goitre", "Struma - goiter", "enlarged thyroid", "goiter (disease)", "THYROID ENLARGED", "Enlarged;thyroid", "Thyroid enlarged", "Enlarged thyroid", "Struma of thyroid", "Goiter (disorder)", "goiter (diagnosis)", "Goitre, unspecified", "Goiter, unspecified", "THYROID ENLARGEMENT", "thyroid enlargement", "Enlargement;thyroid", "Thyroid enlargement", "enlargement; thyroid", "thyroid; enlargement", "enlargement of thyroid", "enlarged thyroid gland", "swelling thyroid gland", "Thyroid gland swelling", "Enlarged thyroid gland", "thyroid gland swelling", "Enlargement of thyroid", "thyroid disorders goiter", "Swelling of thyroid gland", "Goiter (excluding T85 T86)", "enlargement under Adam's apple", "Enlarged thyroid gland in neck", "Enlarged thyroid gland (finding)", "enlargement under Adam's apple (symptom)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "goiter", "shortest_name_length": 6}
{"curie": "UMLS:C4054651", "names": ["Leptospiral Nephropathy", "Leptospirosis Nephropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leptospirosis Nephropathy", "shortest_name_length": 23}
{"curie": "UMLS:C1167732", "names": ["pleuropericarditis", "Pleuropericarditis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pleuropericarditis", "shortest_name_length": 18}
{"curie": "UMLS:C0332865", "names": ["congenital dysplasia", "Congenital Dysplasia", "Dysplasia, congenital", "Congenital dysplasia, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Dysplasia", "shortest_name_length": 20}
{"curie": "UMLS:C4054114", "names": ["Recurrent Adult Undifferentiated High Grade Pleomorphic Sarcoma", "Recurrent Undifferentiated High Grade Pleomorphic Sarcoma of Bone", "Recurrent Adult Undifferentiated High Grade Pleomorphic Sarcoma of Bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Adult Undifferentiated High Grade Pleomorphic Sarcoma of Bone", "shortest_name_length": 63}
{"curie": "MONDO:0044871", "names": ["FTSD", "Musician's cramp", "musician's cramp", "occupational cramp", "Occupational Cramp", "Focal Hand Dystonia", "Focal hand dystonia", "focal hand dystonia", "MUSICIAN'S DYSTONIA", "Musician's Dystonia", "musician's dystonia", "Occupational dystonia", "Occupational Dystonia", "occupational dystonia", "task-specific dystonia", "Task-Specific Dystonia", "occupational; cramp(s)", "cramp(s); occupational", "Task-Specific Focal Dystonia", "task-specific focal dystonia", "Focal Task-Specific Dystonia", "focal task-specific dystonia", "dystonia, focal, task-specific", "Dystonia, Focal, Task-Specific", "DYSTONIA, FOCAL, TASK-SPECIFIC", "Occupational dystonia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dystonia, focal, task-specific", "shortest_name_length": 4}
{"curie": "MONDO:0005214", "names": ["sarcoma vulva", "vulva sarcoma", "Vulvar Sarcoma", "VULVA, SARCOMA", "vulvar sarcoma", "sarcoma of vulva", "Sarcoma of vulva", "VULVAR CANCER, SARCOMA", "mammalian vulva sarcoma", "sarcoma of mammalian vulva", "Sarcoma of vulva (disorder)", "sarcoma of vulva (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulva sarcoma", "shortest_name_length": 13}
{"curie": "UMLS:C0031028", "names": ["Periapical Disease", "periapical disease", "Periapical disease", "Periapical diseases", "Periapical Diseases", "Disease, Periapical", "Diseases, Periapical", "Periradicular disease", "Periapical tissue disease", "periapical; tissues disorder", "Disorder of periapical tissues of tooth", "disease (or disorder); periapical tissues", "Disease of periapical tissues of tooth, NOS", "Disorder of periapical tissues of tooth (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Periapical Diseases", "shortest_name_length": 18}
{"curie": "MONDO:0044622", "names": ["EMILIN-1-related connective tissue disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "EMILIN-1-related connective tissue disease", "shortest_name_length": 42}
{"curie": "UMLS:C5420780", "names": ["Locally Advanced Adrenal Cortex Carcinoma", "Locally Advanced Adrenal Cortical Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Adrenal Cortical Carcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0019659", "names": ["Pfeiffer syndrome type 1", "classic Pfeiffer syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pfeiffer syndrome type 1", "shortest_name_length": 24}
{"curie": "MONDO:0043170", "names": ["Pavone Fiumara Rizzo syndrome", "Syndactyly type 1 with cataracts and mental retardation", "syndactyly type 1 with cataracts and mental retardation", "syndactyly type 1 with cataracts and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pavone Fiumara Rizzo syndrome", "shortest_name_length": 29}
{"curie": "MONDO:0011995", "names": ["cataract - congenital heart disease - neural tube defect syndrome", "craniofacial abnormalities, cataracts, congenital heart disease, sacral neural tube defects, and growth and developmental retardation", "Craniofacial Abnormalities, Cataracts, Congenital Heart Disease, Sacral Neural Tube Defects, and Growth and Developmental Retardation", "CRANIOFACIAL ABNORMALITIES, CATARACTS, CONGENITAL HEART DISEASE, SACRAL NEURAL TUBE DEFECTS, AND GROWTH AND DEVELOPMENTAL RETARDATION", "craniofacial abnormalities, cataracts, congenital heart disease, sacral neural tube defects, and growth and developintellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract - congenital heart disease - neural tube defect syndrome", "shortest_name_length": 65}
{"curie": "MONDO:0033673", "names": ["SPGF46", "spermatogenic failure 46", "SPERMATOGENIC FAILURE 46"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 46", "shortest_name_length": 6}
{"curie": "MONDO:0020576", "names": ["skin vasculitis", "vasculitis skin", "vasculitis; skin", "skin; vasculitis", "Skin vasculitides", "Skin vasculitis NOS", "SKIN VASCULITIS NOS", "vasculitis cutaneous", "cutaneous vasculitis", "Cutaneous vasculitis", "Cutaneous Vasculitis", "Vasculitis, Cutaneous", "Vasculitis in the skin", "vasculitis of the skin", "Vasculitis of the skin", "Cutaneous Vasculitides", "Vasculitis of the skin, NOS", "Vasculitis of the skin (disorder)", "Vasculitis limited to skin, unspecified", "Vasculitis limited to the skin, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous vasculitis", "shortest_name_length": 15}
{"curie": "MONDO:0008682", "names": ["DDS", "NPHS4", "DRASH SYNDROME", "Drash Syndrome", "Drash syndrome", "Syndrome, Drash", "Denys Drash syndrome", "Denys Drash Syndrome", "denys drash syndrome", "denys-drash syndrome", "Denys-Drash syndrome", "Denys-Drash Syndrome", "DENYS-DRASH SYNDROME", "Syndrome, Denys-Drash", "Wilms tumor-DSD syndrome", "Drash syndrome (disorder)", "Nephrotic Syndrome Type 4", "NEPHROTIC SYNDROME TYPE 4", "nephrotic syndrome type 4", "NEPHROTIC SYNDROME, TYPE 4", "nephrotic syndrome congenital type 4", "Wilms tumor and pseudohermaphroditism", "Wilms Tumor and Pseudohermaphroditism", "Nephrotic syndrome with pseudohermaphroditism", "NEPHROPATHY, WILMS TUMOR, AND GENITAL ANOMALIES", "nephropathy, Wilms tumor, and genital anomalies", "Wilms tumor and pseudo- or true hermaphroditism", "Nephropathy, Wilms Tumor, and Genital Anomalies", "WILMS TUMOR AND PSEUDO- OR TRUE HERMAPHRODITISM", "nephrotic syndrome congenital type 4 (diagnosis)", "Wilms tumor-disorder of sex development syndrome", "Pseudohermaphroditism, Nephron Disorder and Wilms' Tumor", "pseudohermaphroditism, nephron disorder and Wilms' tumor", "Denys-Drash syndrome, autosomal dominant, somatic mutation", "Wilms' tumor and nephrotic syndrome with pseudohermaphroditism", "Wilms' tumour and nephrotic syndrome with pseudohermaphroditism", "nephropathy associated with male pseudohermaphroditism and Wilms' tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Denys-Drash syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C5238255", "names": ["AML with RAM Immunophenotype", "Acute Myeloid Leukemia with RAM Immunophenotype"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Myeloid Leukemia with RAM Immunophenotype", "shortest_name_length": 28}
{"curie": "UMLS:C4521801", "names": ["Stage I Anal Cancer", "Stage I Anal Cancer AJCC v8", "Stage I Anal Carcinoma AJCC v8", "Stage I Anal Canal and Perianal (Anal Margin) Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Anal Cancer AJCC v8", "shortest_name_length": 19}
{"curie": "MONDO:0019406", "names": ["craniofacial conodysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniofacial conodysplasia", "shortest_name_length": 26}
{"curie": "UMLS:C3146249", "names": ["Stage IV Renal Cell Cancer", "Stage IV Renal Cell Carcinoma", "Stage IV Renal Cell Cancer AJCC v7", "Stage IV Renal Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Renal Cell Cancer AJCC v7", "shortest_name_length": 26}
{"curie": "MONDO:0015852", "names": ["excess breast volume or number"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "excess breast volume or number", "shortest_name_length": 30}
{"curie": "UMLS:C4727220", "names": ["Metastatic Cervical Adenosquamous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Cervical Adenosquamous Carcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0030067", "names": ["TCS4", "Treacher Collins syndrome 4", "treacher collins syndrome 4", "TREACHER COLLINS SYNDROME 4", "Treacher-Collins syndrome 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Treacher Collins syndrome 4", "shortest_name_length": 4}
{"curie": "UMLS:C1720728", "names": ["AIDS-Related Immunoblastic Lymphoma", "AIDS Related Immunoblastic Lymphoma", "AIDS Associated Immunoblastic Lymphoma", "Immunoblastic lymphoma associated with AIDS", "AIDS Related Immunoblastic Large Cell Lymphoma", "AIDS-related immunoblastic large cell lymphoma", "immunoblastic large cell lymphoma, AIDS-related", "AIDS-associated immunoblastic large cell lymphoma", "AIDS-Associated Immunoblastic Large Cell Lymphoma", "Immunoblastic lymphoma associated with AIDS (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immunoblastic lymphoma associated with AIDS", "shortest_name_length": 35}
{"curie": "MONDO:0024257", "names": ["genetic motor neuron disease", "Familial motor neuron disease", "motor neuron disease familial", "Familial Motor Neuron Disease", "Motor Neuron Disease, Familial", "hereditary motor neuron disease", "Hereditary motor neuron disease", "Hereditary motor neurone disease", "Spinal hereditary muscular atrophy", "Familial motor neuron disease, NOS", "genetic anterior horn cell disease", "muscle; atrophy, spinal, hereditary", "atrophy; muscle, spinal, hereditary", "Hereditary motor neuron disease, NOS", "Familial motor neuron disease (diagnosis)", "Hereditary motor neuron disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary motor neuron disease", "shortest_name_length": 28}
{"curie": "MONDO:0010581", "names": ["NDI", "Ndi", "NDI1", "nephrogenic diabetes insipidus type 1", "Nephrogenic Diabetes Insipidus, Type I", "X-linked nephrogenic diabetes insipidus", "DIABETES INSIPIDUS, NEPHROGENIC, TYPE I", "Diabetes Insipidus, Nephrogenic, Type 1", "diabetes insipidus, nephrogenic, type 1", "Diabetes Insipidus, Nephrogenic, Type I", "nephrogenic diabetes insipidus, x-linked", "Diabetes Insipidus, Nephrogenic, X-Linked", "diabetes insipidus, nephrogenic, X-linked", "DIABETES INSIPIDUS, NEPHROGENIC, 1, X-LINKED", "nephrogenic diabetes insipidus, x-linked (diagnosis)", "diabetes insipidus, nephrogenic, 1, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diabetes insipidus, nephrogenic, X-linked", "shortest_name_length": 3}
{"curie": "MONDO:0002899", "names": ["Differentiating", "Differentiating Neuroblastoma", "differentiating neuroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "differentiating neuroblastoma", "shortest_name_length": 15}
{"curie": "UMLS:C0858318", "names": ["p falciparum", "p.falciparum", "Plasmodium falciparum infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Plasmodium falciparum infection", "shortest_name_length": 12}
{"curie": "UMLS:C5557149", "names": ["Stage I Cervical Cancer AJCC v9", "Stage I Cervical Carcinoma AJCC v9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Cervical Cancer AJCC v9", "shortest_name_length": 31}
{"curie": "UMLS:C0020800", "names": ["immunoglobulin hypercatabolism", "Immunoglobulin hypercatabolism", "Idiopathic hypercatabolic hypoproteinemia", "Immunoglobulin hypercatabolism (disorder)", "Idiopathic Hypercatabolic Hypoproteinemia", "Hypercatabolic Hypoproteinemia, Idiopathic", "Hypoproteinemia, Idiopathic Hypercatabolic", "Idiopathic hypercatabolic hypoproteinaemia", "immunoglobulin hypercatabolism (diagnosis)", "Idiopathic Hypercatabolic Hypoproteinemias", "Hypercatabolic Hypoproteinemias, Idiopathic", "Hypoproteinemias, Idiopathic Hypercatabolic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Idiopathic Hypercatabolic Hypoproteinemia", "shortest_name_length": 30}
{"curie": "UMLS:C4683667", "names": ["Primary Mediastinal (Thymic) Large B-Cell Lymphoma by Ann Arbor Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Mediastinal (Thymic) Large B-Cell Lymphoma by Ann Arbor Stage", "shortest_name_length": 69}
{"curie": "UMLS:C4525261", "names": ["Stage IB Intrahepatic Bile Duct Cancer", "stage IB intrahepatic bile duct cancer", "stage IB intrahepatic bile duct cancer AJCC v8", "Stage IB Intrahepatic Bile Duct Cancer AJCC v8", "Stage IB Intrahepatic Bile Duct Carcinoma AJCC v8", "stage IB intrahepatic bile duct carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Intrahepatic Bile Duct Cancer AJCC v8", "shortest_name_length": 38}
{"curie": "MONDO:0022746", "names": ["trisomy 13p", "Trisomy 13p", "Duplication 13p", "chromosome 13p, trisomy", "Chromosome 13p, trisomy", "Chromosome 13p duplication", "chromosome 13p duplication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 13p duplication", "shortest_name_length": 11}
{"curie": "MONDO:0032898", "names": ["SPGF43", "spermatogenic failure 43", "SPERMATOGENIC FAILURE 43"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 43", "shortest_name_length": 6}
{"curie": "OMIM:248310", "names": ["PFBI", "PLASMODIUM FALCIPARUM PARASITEMIA", "PLASMODIUM FALCIPARUM BLOOD INFECTION LEVEL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 4}
{"curie": "UMLS:C4553748", "names": ["Stage IV Bladder Cancer", "Stage IV Bladder Cancer AJCC v8", "Stage IV Bladder Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Bladder Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "UMLS:C1336211", "names": ["Stage IIIA Lung Cancer", "Stage IIIA Lung Carcinoma", "Stage IIIA Carcinoma of Lung", "Stage IIIA Lung Cancer AJCC v7", "Stage IIIA Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Lung Cancer AJCC v7", "shortest_name_length": 22}
{"curie": "MONDO:0004899", "names": ["microtropia", "microstrabismus", "monofixation syndrome", "Monofixation syndrome", "syndrome; monofixation", "monofixation; syndrome", "Monofixation syndrome (disorder)", "monofixation syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "monofixation syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0006390", "names": ["PRSCC", "Prostate Small Cell NEC", "prostate small cell NEC", "prostate oat cell carcinoma", "prostate Oat cell carcinoma", "Prostate Oat Cell Carcinoma", "Prostate Small Cell Carcinoma", "carcinoma cell prostate small", "prostate small cell carcinoma", "Oat cell carcinoma of prostate", "Oat Cell Carcinoma of Prostate", "Small Cell Carcinoma of Prostate", "small cell carcinoma of prostate", "Small cell carcinoma of prostate", "Oat Cell Carcinoma of the Prostate", "Oat cell carcinoma of the prostate", "prostate gland small cell carcinoma", "small cell carcinoma of the prostate", "Small Cell Carcinoma of the Prostate", "small cell carcinoma of prostate gland", "Small cell carcinoma of prostate (disorder)", "Prostate Small Cell Neuroendocrine Carcinoma", "prostate small cell neuroendocrine carcinoma", "Small cell neuroendocrine carcinoma of prostate", "small cell carcinoma of prostate gland (diagnosis)", "Small cell neuroendocrine carcinoma of prostate (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate small cell carcinoma", "shortest_name_length": 5}
{"curie": "UMLS:C0334035", "names": ["Glandular metaplasia", "Glandular Metaplasia", "Glandular Metaplasias", "Metaplasia, glandular", "GLANDULAR METAPLASIAS", "Glandular metaplasia, NOS", "Glandular metaplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Glandular metaplasia", "shortest_name_length": 20}
{"curie": "MONDO:0012566", "names": ["AUTS11", "autism susceptibility 11", "autism, susceptibility to, 11", "AUTISM, SUSCEPTIBILITY TO, 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autism, susceptibility to, 11", "shortest_name_length": 6}
{"curie": "UMLS:C1328383", "names": ["Listeria sepsis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Listeria sepsis", "shortest_name_length": 15}
{"curie": "MONDO:0011532", "names": ["SPG13", "spastic paraplegia 13", "hereditary spastic paraplegia 13", "HSPD1 hereditary spastic paraplegia", "hereditary spastic paraplegia type 13", "autosomal dominant spastic paraplegia 13", "SPASTIC PARAPLEGIA 13, AUTOSOMAL DOMINANT", "Spastic paraplegia 13, autosomal dominant", "spastic paraplegia 13, autosomal dominant", "autosomal dominant spastic paraplegia type 13", "Autosomal dominant spastic paraplegia type 13", "Autosomal dominant spastic paraplegia type 13 (disorder)", "hereditary spastic paraplegia caused by mutation in HSPD1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 13", "shortest_name_length": 5}
{"curie": "MONDO:0015778", "names": ["syndromic hypothyroidism", "syndrome associated with hypothyroidism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic hypothyroidism", "shortest_name_length": 24}
{"curie": "MONDO:0024772", "names": ["MRXSP", "syndromic X-linked intellectual disability Pilorge type", "intellectual developmental disorder, X-linked, syndromic, Pilorge type", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, PILORGE TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder, X-linked, syndromic, Pilorge type", "shortest_name_length": 5}
{"curie": "UMLS:C0855104", "names": ["Burkitt's tumor recurrent", "Recurrent Burkitt Lymphoma", "Burkitt's tumour recurrent", "Relapsed Burkitt's Lymphoma", "Burkitt's lymphoma recurrent", "Recurrent Burkitt's Lymphoma", "Burkitt's tumor or lymphoma recurrent", "Burkitt's tumour or lymphoma recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Burkitt Lymphoma", "shortest_name_length": 25}
{"curie": "UMLS:C1278807", "names": ["chlamydia urethritis", "Chlamydia urethritis", "Urethritis;chlamydial", "chlamydial urethritis", "Urethritis chlamydial", "CHLAMYDIAL URETHRITIS", "URETHRITIS CHLAMYDIAL", "Chlamydial urethritis", "Chlamydia trachomatis urethritis", "NGU due to Chlamydia trachomatis", "Chlamydial urethritis (disorder)", "urethritis due to Chlamydia trachomatis", "Urethritis due to Chlamydia trachomatis", "Chlamydia trachomatis urethritis reaction", "Urethritis caused by Chlamydia trachomatis", "urethritis due to Chlamydia trachomatis (diagnosis)", "Other nongonococcal urethritis, chlamydia trachomatis", "Urethritis caused by Chlamydia trachomatis (disorder)", "Nongonococcal urethritis due to Chlamydia trachomatis", "Nongonococcal urethritis [NGU] due to Chlamydia trachomatis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chlamydial urethritis", "shortest_name_length": 20}
{"curie": "UMLS:C0266572", "names": ["eyelid; anomaly", "anomaly; eyelid", "congenital eyelid deformity", "Eyelid disorders congenital", "Congenital eyelid deformity", "Congenital anomaly of eyelid", "eyelid; deformity, congenital", "deformity; eyelid, congenital", "Congenital Eyelid Malformation", "congenital anomalies of eyelid", "Congenital eyelid malformation", "Developmental anomaly of eyelid", "Congenital abnormality of eyelid", "Congenital anomaly of eyelid, NOS", "Congenital deformities of eyelids", "Congenital malformation of eyelid", "Congenital eyelid malformation NOS", "Eyelid malformation, congenital NOS", "Congenital malformation of eyelid NOS", "Congenital malformation of the eyelid", "congenital eyelid deformity (diagnosis)", "Congenital anomaly of eyelid (disorder)", "congenital anomalies of eyelid (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital anomaly of eyelid", "shortest_name_length": 15}
{"curie": "UMLS:C0855199", "names": ["Testicular germ cell tumor mixed stage II", "Stage II Testicular Mixed Germ Cell Tumor", "Testicular germ cell tumour mixed stage II", "Stage II Testicular Mixed Germ Cell Tumor AJCC v7", "Stage II Testicular Mixed Germ Cell Tumor AJCC v6", "Stage II Testicular Mixed Germ Cell Tumor AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular germ cell tumor mixed stage II", "shortest_name_length": 41}
{"curie": "MONDO:0009292", "names": ["GSD4", "GSD 4", "gsd iv", "GSD IV", "Andersen", "GSD type 4", "GSD type IV", "glycogenosis 4", "Glycogenosis 4", "GLYCOGENOSIS IV", "amylopectinosis", "Gbe1 Deficiency", "Amylopectinoses", "Glycogenosis 4s", "Gbe1 deficiency", "AMYLOPECTINOSIS", "GBE1 DEFICIENCY", "Glycogenosis IV", "Amylopectinosis", "Andersen disease", "Andersen Disease", "andersen disease", "Deficiency, Gbe1", "Glycogenosis IVs", "ANDERSEN DISEASE", "Gbe1 Deficiencies", "Disease, Andersen", "Andersens Disease", "Andersen's Disease", "Andersen's disease", "Deficiencies, Gbe1", "andersen's disease", "brancher deficiency", "glycogenosis type 4", "Glycogenosis type 4", "BRANCHER DEFICIENCY", "Disease, Andersen's", "Brancher Deficiency", "Deficiency, Brancher", "Type IV Glycogenoses", "Glycogenosis, type 4", "glycogenosis type iv", "Glycogenosis type IV", "glycogenosis type IV", "Type IV Glycogenosis", "Glycogenosis, Type IV", "Brancher Deficiencies", "GLYCOGENOSIS, TYPE IV", "Glycogenoses, Type IV", "Deficiencies, Brancher", "GSD IV, CLASSIC HEPATIC", "GSD IV, Classic Hepatic", "GSD IV, classic hepatic", "BRANCHER ENZYME DEFICIENCY", "glycogen storage disease 4", "Glycogen storage disease 4", "brancher enzyme; deficiency", "glycogen storage disease IV", "GLYCOGEN STORAGE DISEASE IV", "Branching enzyme deficiency", "deficiency; brancher enzyme", "GBE1 glycogen storage disease", "GSD IV, nonprogressive hepatic", "GSD IV, Nonprogressive Hepatic", "Andersen disease (GSD type IV)", "Deficiency of branching enzyme", "GSD IV, NONPROGRESSIVE HEPATIC", "glycogen storage disease type 4", "Glycogen Storage Disease Type 4", "Glycogen storage disease type 4", "glycogen storage disease type IV", "glycogen storage disease type iv", "Glycogen storage disease, type 4", "Glycogen Storage Disease Type IV", "brancher deficiency glycogenosis", "Glycogen storage disease type IV", "GLYCOGEN STORAGE DISEASE TYPE IV", "type iv glycogen storage disease", "Glycogen storage disease, type IV", "brancher glycogen storage disease", "Brancher glycogen storage disease", "glycogen storage disease, type IV", "BRANCHER DEFICIENCY AMYLOPECTINOSIS", "Glycogen Branching Enzyme Deficiency", "glycogen branching enzyme deficiency", "GLYCOGEN BRANCHING ENZYME DEFICIENCY", "GSD IV, neuromuscular form, childhood", "GSD IV, neuromuscular form, congenital", "Andersen disease (GSD type IV) (diagnosis)", "GSD IV, neuromuscular form, fatal perinatal", "Brancher deficiency glycogen storage disease", "Glycogen storage disease, type IV (disorder)", "Deficiency of amylo-(1,4,6)-transglycosylase", "Branching-transferase deficiency glycogenosis", "branching-transferase deficiency glycogenosis", "deficiency of 1,4-alpha-glucan branching enzyme", "Deficiency of 1,4-alpha-glucan branching enzyme", "GSD due to glycogen branching enzyme deficiency", "Andersen disease (glycogen storage disease type IV)", "glycogen storage disease caused by mutation in GBE1", "1,4,alpha-glucan 6-alpha-glucosyltransferase deficiency", "glycogenosis due to glycogen branching enzyme deficiency", "Glycogenosis due to glycogen branching enzyme deficiency", "GSD IV, Neuromuscular Form, Adult, with Isolated Myopathy", "GSD IV, neuromuscular form, adult, with isolated myopathy", "CIRRHOSIS, FAMILIAL, WITH DEPOSITION OF ABNORMAL GLYCOGEN", "GSD IV, NEUROMUSCULAR FORM, ADULT, WITH ISOLATED MYOPATHY", "Cirrhosis, familial, with deposition of abnormal glycogen", "cirrhosis, familial, with deposition of abnormal glycogen", "Deficiency of 1,4-alpha-glucan branching enzyme (disorder)", "glycogen storage disease due to glycogen branching enzyme deficiency", "Glycogen storage disease due to glycogen branching enzyme deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease due to glycogen branching enzyme deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0007643", "names": ["IgA, defect in Assembly of", "IgA, DEFECT IN ASSEMBLY OF", "IgA, Defect in Assembly of", "Gamma-A-Globulin, Defect in Assembly of", "Immunoglobulin A, Defect in Assembly of", "IMMUNOGLOBULIN A, DEFECT IN ASSEMBLY OF", "GAMMA-A-GLOBULIN, DEFECT IN ASSEMBLY OF", "Immunoglobulin A, defect in Assembly of", "gamma-A-globulin, defect in assembly of", "gamma-A-globulin, defect in ASSEMBLY OF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gamma-A-globulin, defect in assembly of", "shortest_name_length": 26}
{"curie": "MONDO:0010859", "names": ["AVSD3", "atrioventricular septal defect 3", "ATRIOVENTRICULAR SEPTAL DEFECT 3", "GJA1 atrioventricular septal defect", "atrioventricular septal defect type 3", "atrioventricular septal defect caused by mutation in GJA1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrioventricular septal defect 3", "shortest_name_length": 5}
{"curie": "MONDO:0005552", "names": ["ocular vascular disease", "ocular vascular disorder", "Ocular vascular disorder", "Ocular Vascular Disorder", "vasculature of eye disease", "disease of vasculature of eye", "disorder of vasculature of eye", "vasculature of eye disease or disorder", "disease or disorder of vasculature of eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ocular vascular disorder", "shortest_name_length": 23}
{"curie": "MONDO:0005949", "names": ["Roseolovirus infection", "Roseolovirus Infection", "Roseolovirus Infections", "Infection, Roseolovirus", "Infections, Roseolovirus", "Roseolovirus infectious disease", "roseolovirus infectious disease", "Roseolovirus disease or disorder", "Infection caused by Roseolovirus", "Roseolovirus caused disease or disorder", "Infection caused by Roseolovirus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "roseolovirus infectious disease", "shortest_name_length": 22}
{"curie": "MONDO:0003098", "names": ["Mediastinal Neural Tumor", "mediastinal neural tumor", "mediastinal neural neoplasm", "Mediastinal Neural Neoplasm", "Mediastinal Neurogenic Tumor", "mediastinal neurogenic tumor", "Neurogenic Tumor of Mediastinum", "mediastinal neurogenic neoplasm", "neurogenic tumor of mediastinum", "Mediastinal Neurogenic Neoplasm", "Neurogenic Neoplasm of Mediastinum", "neurogenic neoplasm of mediastinum", "neurogenic tumor of the mediastinum", "Neurogenic Tumor of the Mediastinum", "neurogenic neoplasm of the mediastinum", "Neurogenic Neoplasm of the Mediastinum", "malignant mediastinal neurogenic neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mediastinal neural neoplasm", "shortest_name_length": 24}
{"curie": "MONDO:0017247", "names": ["communicating congenital bronchopulmonary-foregut malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "communicating congenital bronchopulmonary-foregut malformation", "shortest_name_length": 62}
{"curie": "UMLS:C5556662", "names": ["HPV-Independent Cervical Squamous Cell Carcinoma", "Human Papillomavirus-Independent Cervical Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Human Papillomavirus-Independent Cervical Squamous Cell Carcinoma", "shortest_name_length": 48}
{"curie": "MONDO:0019900", "names": ["non-distal deletion 12q", "non-distal monosomy 12q", "non-telomeric monosomy 12q", "non-distal monosomy type 12q"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-distal monosomy 12q", "shortest_name_length": 23}
{"curie": "UMLS:C1696575", "names": ["Wet injection", "Injection site discharge"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site discharge", "shortest_name_length": 13}
{"curie": "UMLS:C5420185", "names": ["Laryngeal Large Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laryngeal Large Cell Neuroendocrine Carcinoma", "shortest_name_length": 45}
{"curie": "MONDO:0016879", "names": ["partial deletion of chromosome 17", "partial monosomy of chromosome 17", "partial deletion of chromosome type 17"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of chromosome 17", "shortest_name_length": 33}
{"curie": "MONDO:0018529", "names": ["qualitative or quantitative defects of Torsin-1A-interacting protein 1", "qualitative or quantitative defects of Torsin-1A-interacting protein type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of Torsin-1A-interacting protein 1", "shortest_name_length": 70}
{"curie": "UMLS:C4521947", "names": ["Stage IV Sinonasal Cancer AJCC v7", "Stage IV Sinonasal Carcinoma AJCC v7", "Stage IV Nasal Cavity and Paranasal Sinus Cancer", "Stage IV Nasal Cavity and Paranasal Sinus Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Nasal Cavity and Paranasal Sinus Cancer AJCC v7", "shortest_name_length": 33}
{"curie": "MONDO:0014354", "names": ["MRT43", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 43", "mental retardation, autosomal recessive 43", "intellectual disability, autosomal recessive 43", "mental retardation, autosomal recessive type 43", "intellectual disability, autosomal recessive type 43", "autosomal recessive intellectual developmental disorder 43", "intellectual developmental disorder, autosomal recessive 43", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 43", "WASHC4 autosomal recessive non-syndromic intellectual disability", "autosomal recessive non-syndromic intellectual disability caused by mutation in WASHC4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 43", "shortest_name_length": 5}
{"curie": "MONDO:0044762", "names": ["motility-related diarrhea", "diarrhea from increased bowel motility", "diarrheal disease secondary to increased bowel motility"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diarrheal disease secondary to increased bowel motility", "shortest_name_length": 25}
{"curie": "UMLS:C3900120", "names": ["Acquired Facial Nerve Palsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired Facial Nerve Palsy", "shortest_name_length": 27}
{"curie": "MONDO:0011320", "names": ["Tsukahara syndrome", "Giuffré-Tsukahara syndrome", "Giuffre-Tsukahara syndrome", "GIUFFRE-TSUKAHARA SYNDROME", "radioulnar synostosis-microcephaly-scoliosis syndrome", "radioulnar synostosis with microcephaly, short stature, scoliosis, and mental retardation", "RADIOULNAR SYNOSTOSIS WITH MICROCEPHALY, SHORT STATURE, SCOLIOSIS, AND MENTAL RETARDATION", "radioulnar synostosis with microcephaly, short stature, scoliosis, and intellectual disability", "RADIOULNAR SYNOSTOSIS WITH MICROCEPHALY, SHORT STATURE, SCOLIOSIS, AND INTELLECTUAL DEVELOPMENTAL DISORDER", "Tsukahara syndrome of radioulnar synostosis, short stature, microcephaly, scoliosis, and mental retardation", "Tsukahara syndrome of radioulnar synostosis, short stature, microcephaly, scoliosis, and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radioulnar synostosis-microcephaly-scoliosis syndrome", "shortest_name_length": 18}
{"curie": "UMLS:C0496905", "names": ["neoplasm uncertain behavior stomach", "Neoplasm of uncertain behavior of stomach", "neoplasm of uncertain behavior of stomach", "Neoplasm of uncertain behaviour of stomach", "Neoplasm of uncertain behavior of stomach, NOS", "Neoplasm of uncertain behaviour of stomach, NOS", "Neoplasm of uncertain behavior of stomach (disorder)", "Neoplasm of uncertain or unknown behavior of stomach", "neoplasm of uncertain behavior of stomach (diagnosis)", "Neoplasm of uncertain or unknown behaviour of stomach"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplasm of uncertain or unknown behavior of stomach", "shortest_name_length": 35}
{"curie": "UMLS:C0948806", "names": ["Catheter related complication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Catheter related complication", "shortest_name_length": 29}
{"curie": "UMLS:C1096701", "names": ["Medical device discomfort"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Medical device discomfort", "shortest_name_length": 25}
{"curie": "MONDO:0004226", "names": ["diffuse intraductal papillomatosis", "Diffuse intraductal papillomatosis", "Diffuse Intraductal Papillomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diffuse intraductal papillomatosis", "shortest_name_length": 34}
{"curie": "UMLS:C1619733", "names": ["Gout flare"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gout flare", "shortest_name_length": 10}
{"curie": "MONDO:0010122", "names": ["TTP", "USS", "Familial TTP", "familial TTP", "congenital TTP", "Congenital TTP", "TTP, congenital", "Familial TTP/HUS", "Schulman-Upshaw syndrome", "Upshaw-Schulman Syndrome", "Schulman Upshaw Syndrome", "UPSHAW-SCHULMAN SYNDROME", "Schulman-Upshaw Syndrome", "Upshaw-Schulman syndrome", "Upshaw Schulman Syndrome", "SCHULMAN-UPSHAW SYNDROME", "Upshaw Factor, deficiency of", "Upshaw Factor, Deficiency of", "UPSHAW FACTOR, DEFICIENCY OF", "Congenital ADAMTS13 Deficiency", "congenital ADAMTS13 deficiency", "Congenital ADAMTS-13 deficiency", "Congenital ADAMTS-13 Deficiency", "congenital ADAMTS-13 deficiency", "MICROANGIOPATHIC HEMOLYTIC ANEMIA", "Microangiopathic hemolytic Anemia", "Familial Thrombotic Microangiopathy", "Upshaw-Schulman syndrome (disorder)", "Microangiopathy, Familial Thrombotic", "thrombotic microangiopathy, familial", "Thrombotic Microangiopathy, Familial", "THROMBOTIC MICROANGIOPATHY, FAMILIAL", "Familial Thrombotic Thrombocytopenic Purpura", "Familial Thrombotic Thrombocytopenia Purpura", "thrombotic thrombocytopenic purpura, familial", "Microangiopathic hemolytic Anemia, congenital", "THROMBOTIC THROMBOCYTOPENIC PURPURA, FAMILIAL", "Thrombotic Thrombocytopenic Purpura, Familial", "MICROANGIOPATHIC HEMOLYTIC ANEMIA, CONGENITAL", "Microangiopathic Hemolytic Anemia, Congenital", "congenital thrombotic thrombocytopenic purpura", "hereditary thrombotic thrombocytopenic purpura", "Congenital thrombotic thrombocytopenic purpura", "Congenital Thrombotic Thrombocytopenic Purpura", "thrombotic thrombocytopenic purpura, congenital", "Thrombotic Thrombocytopenic Purpura, Congenital", "THROMBOTIC THROMBOCYTOPENIC PURPURA, CONGENITAL", "thrombotic thrombocytopenic purpura, hereditary", "THROMBOTIC THROMBOCYTOPENIC PURPURA, HEREDITARY", "Familial thrombotic thrombocytopenic purpura / hemolytic uremic syndrome", "THROMBOTIC THROMBOCYTOPENIC PURPURA, HEREDITARY, INFANTILE- OR ADULT-ONSET", "Familial thrombotic thrombocytopenic purpura / haemolytic uraemic syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital thrombotic thrombocytopenic purpura", "shortest_name_length": 3}
{"curie": "MONDO:0016809", "names": ["SCAE", "MSCAE", "Spinocerebellar ataxia with epilepsy", "Spinocerebellar Ataxia with Epilepsy", "spinocerebellar ataxia with epilepsy", "SPINOCEREBELLAR ATAXIA WITH EPILEPSY", "Myoclonic epilepsy myopathy sensory ataxia", "Myoclonic Epilepsy Myopathy Sensory Ataxia", "MEMSA - myoclonic epilepsy myopathy sensory ataxia", "Mitochondrial spinocerebellar ataxia with epilepsy", "mitochondrial spinocerebellar ataxia with epilepsy", "Myoclonic epilepsy myopathy sensory ataxia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia with epilepsy", "shortest_name_length": 4}
{"curie": "MONDO:0011178", "names": ["ICCA", "PKD/IC", "Icca syndrome", "ICCA Syndrome", "ICCA SYNDROME", "ICCA syndrome", "infantile convulsions and choreoathetosis", "Infantile convulsions and choreoathetosis", "ICCA Infantile convulsions and choreoathetosis", "Infantile convulsion and choreoathetosis syndrome", "Paroxysmal kinesigenic dyskinesia and infantile convulsion", "paroxysmal kinesigenic dyskinesia and infantile convulsions", "Paroxysmal kinesigenic dyskinesia and infantile convulsions", "Infantile convulsion and choreoathetosis syndrome (disorder)", "paroxysmal kinesigenic dyskinesia with infantile convulsions", "Paroxysmal Kinesigenic Dyskinesia with Infantile Convulsions", "PAROXYSMAL KINESIGENIC DYSKINESIA WITH INFANTILE CONVULSIONS", "INFANTILE CONVULSIONS AND PAROXYSMAL CHOREOATHETOSIS, FAMILIAL", "Infantile Convulsions and Paroxysmal Choreoathetosis, Familial", "Infantile convulsions and paroxysmal choreoathetosis, familial", "infantile convulsions and paroxysmal choreoathetosis, familial", "convulsions, familial infantile, with paroxysmal choreoathetosis", "CONVULSIONS, FAMILIAL INFANTILE, WITH PAROXYSMAL CHOREOATHETOSIS", "convulsions, infantile, with paroxysmal choreoathetosis, familial", "Convulsions, infantile, with paroxysmal choreoathetosis, familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile convulsions and choreoathetosis", "shortest_name_length": 4}
{"curie": "UMLS:C0161819", "names": ["Digestive System Complication", "digestive tract complications", "Gastrointestinal complication", "Gastrointestinal Complication", "Digestive system complications", "Gastrointestinal complications", "gastrointestinal complications", "complications; gastrointestinal", "gastrointestinal; complications", "Gastrointestinal complication, NOS", "Gastrointestinal complication (disorder)", "digestive tract complications (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal complication", "shortest_name_length": 29}
{"curie": "UMLS:C4324374", "names": ["Renal tubular injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal tubular injury", "shortest_name_length": 20}
{"curie": "UMLS:C3899516", "names": ["Complex tic", "Complex Tic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Complex tic", "shortest_name_length": 11}
{"curie": "UMLS:C1334568", "names": ["Malignant Heart Paraganglioma", "Malignant Cardiac Paraganglioma", "Malignant Paraganglioma of Heart", "Metastatic Cardiac Paraganglioma", "Malignant Paraganglioma of the Heart"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Cardiac Paraganglioma", "shortest_name_length": 29}
{"curie": "MONDO:0007184", "names": ["AGA", "AGA1", "Pattern baldness", "Pattern Baldness", "Baldness, Pattern", "Androgenic alopecia", "Androgenic Alopecia", "androgenic alopecia", "Alopecia, Androgenic", "Alopecia, hereditary", "Alopecia hereditaria", "alopecia; androgenic", "androgenic; alopecia", "Androgenic Alopecias", "ANDROGENETIC ALOPECIA", "Alopecias, Androgenic", "Androgenetic alopecia", "Androgenetic Alopecia", "Alopecia, Androgenetic", "baldness, Male pattern", "alopecia, androgenetic, 1", "ALOPECIA, ANDROGENETIC, 1", "Alopecia, Androgenetic, 1", "Atrophic follicular dysplasia", "androgenic alopecia (diagnosis)", "Alopecia hereditaria (disorder)", "Androgenic alopecia, unspecified", "Atrophic follicular dysplasia (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alopecia, androgenetic, 1", "shortest_name_length": 3}
{"curie": "MONDO:0018322", "names": ["HSD10 disease, classic type", "MHBD deficiency, classic type", "HSD10 disease, infantile type", "HSD10 deficiency, classic type", "MHBD deficiency, infantile type", "HSD10 deficiency, infantile type", "2-methyl-3-hydroxybutyric aciduria, classic type", "2-methyl-3-hydroxybutyric aciduria, infantile type", "2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency, classic type", "2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency, infantile type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HSD10 disease, infantile type", "shortest_name_length": 27}
{"curie": "UMLS:C3830526", "names": ["Device embolization", "Device embolisation", "Device Embolization"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Device embolization", "shortest_name_length": 19}
{"curie": "MONDO:0003103", "names": ["nerve root tumor", "Nerve Root Tumor", "nerve Root tumor", "nerve Root tumors", "Nerve Root Tumors", "tumor of nerve root", "tumor of nerve Root", "nerve root neoplasm", "Nerve Root Neoplasm", "Tumor of Nerve Root", "Nerve Root Neoplasms", "nerve Root neoplasms", "neoplasms, nerve Root", "Neoplasms, Nerve Root", "neoplasm of nerve Root", "neoplasm of nerve root", "Neoplasm of Nerve Root", "Tumor of the Nerve Root", "tumor of the nerve Root", "Neoplasm of the Nerve Root", "neoplasm of the nerve Root", "nerve root neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nerve root neoplasm", "shortest_name_length": 16}
{"curie": "UMLS:C5446648", "names": ["Metastatic Endometrial Adenosquamous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Endometrial Adenosquamous Carcinoma", "shortest_name_length": 46}
{"curie": "MONDO:0014811", "names": ["CAVIPMR", "CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION", "cerebellar atrophy, visual impairment, and psychomotor retardation", "cerebellar atrophy, visual impairment, and psychomotor retardation;"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellar atrophy, visual impairment, and psychomotor retardation;", "shortest_name_length": 7}
{"curie": "MONDO:0023232", "names": ["GCM", "myocarditis giant cell", "giant cell myocarditis", "Giant cell myocarditis", "Giant Cell Myocarditis", "Myocarditis, giant cell", "idiopathic giant-cell myocarditis", "Giant cell myocarditis (disorder)", "Giant cell myocarditis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "giant cell myocarditis", "shortest_name_length": 3}
{"curie": "UMLS:C4763794", "names": ["Refractory NK-Cell Lymphoma, Unclassifiable"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory NK-Cell Lymphoma, Unclassifiable", "shortest_name_length": 43}
{"curie": "MONDO:0015833", "names": ["pseudounicornuate uterus", "incomplete unilateral Mullerian aplasia", "incomplete unilateral Müllerian aplasia", "unicornuate uterus with rudimentary horn", "incomplete unilateral aplasia of the Mullerian ducts", "incomplete unilateral aplasia of the Müllerian ducts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudounicornuate uterus", "shortest_name_length": 24}
{"curie": "UMLS:C5555176", "names": ["Refractory Fallopian Tube Transitional Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Fallopian Tube Transitional Cell Carcinoma", "shortest_name_length": 53}
{"curie": "MONDO:0045024", "names": ["neoplasm", "cancer or benign tumor", "cell proliferation disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cancer or benign tumor", "shortest_name_length": 8}
{"curie": "UMLS:C0342153", "names": ["Thyroid Hypoplasia", "Congenital Thyroid Hypoplasia", "Congenital thyroid hypoplasia", "Congenital Thyroid Gland Hypoplasia", "Congenital thyroid hypoplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital thyroid hypoplasia", "shortest_name_length": 18}
{"curie": "MONDO:0017481", "names": ["amelia of lower limb, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amelia of lower limb, bilateral", "shortest_name_length": 31}
{"curie": "UMLS:C0278488", "names": ["stage IV breast cancer", "breast cancer iv stage", "breast cancer stage iv", "Breast cancer stage IV", "breast cancer, stage IV", "breast cancer metastatic", "metastatic breast cancer", "Breast cancer metastatic", "Metastatic breast cancer", "Breast carcinoma stage IV", "Carcinoma breast stage IV", "breast cancer, metastatic", "Breast cancer NOS stage IV", "BREAST CANCER NOS METASTATIC", "Breast carcinoma NOS stage IV"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carcinoma breast stage IV", "shortest_name_length": 22}
{"curie": "MONDO:0011157", "names": ["GLHS", "GLH Syndrome", "GOMEZ-LOPEZ-HERNANDEZ syndrome", "Gomez-Lopez-Hernandez Syndrome", "GOMEZ-LOPEZ-HERNANDEZ SYNDROME", "Gomez-Lopez-Hernández syndrome", "Gomez Lopez Hernandez syndrome", "Gomez-Lopez-Hernandez syndrome", "Gómez-López-Hernández syndrome", "cerebellotrigeminodermal dysplasia", "Gomez and Lopez-Hernandez syndrome", "Cerebellotrigeminal dermal dysplasia", "cerebellotrigeminal-dermal dysplasia", "Cerebellotrigeminal-dermal dysplasia", "Gomez Lopez Hernandez syndrome (disorder)", "Cerebellotrigeminal dermal dysplasia syndrome", "Cerebellotrigeminal-dermal dysplasia syndrome", "cerebellotrigeminal and focal dermal dysplasia", "Craniosynostosis-alopecia-brain defect syndrome", "craniosynostosis-alopecia-brain defect syndrome", "CEREBELLOTRIGEMINAL DERMAL DYSPLASIA CEREBELLO-TRIGEMINAL-DERMAL DYSPLASIA", "Cerebellotrigeminal dermal dysplasia cerebello-trigeminal-dermal dysplasia", "craniosynostosis-ataxia-trigeminal anesthesia-parietal anesthesia and pons-vermis fusion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gomez-Lopez-Hernandez syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0008556", "names": ["cyclic thrombocytopenia", "Cyclic thrombocytopenia", "thrombocytopenia cyclic", "Thrombocytopenia, cyclic", "THROMBOCYTOPENIA, CYCLIC", "thrombocytopenia, cyclic", "tidal platelet dysgenesis", "Tidal platelet dysgenesis", "Cyclic thrombocytopenia (disorder)", "tidal platelet dysgenesis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombocytopenia, cyclic", "shortest_name_length": 23}
{"curie": "UMLS:C1697747", "names": ["Laryngeal bleeding", "Laryngeal Hemorrhage", "Laryngeal hemorrhage", "Laryngeal haemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laryngeal Hemorrhage", "shortest_name_length": 18}
{"curie": "MONDO:0012174", "names": ["Peripheral Cone Dystrophy", "PERIPHERAL CONE DYSTROPHY", "peripheral cone dystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peripheral cone dystrophy", "shortest_name_length": 25}
{"curie": "UMLS:C0279581", "names": ["L2 pediatric ALL", "L2 childhood ALL", "ALL, childhood L2", "childhood ALL, L2", "ALL, L2 childhood", "ALL, L2 pediatric", "ALL, pediatric L2", "pediatric ALL, L2", "L2 Acute Lymphoblastic Leukemia", "L2 pediatric acute lymphocytic leukemia", "L2 childhood acute lymphocytic leukemia", "childhood acute lymphocytic leukemia, L2", "acute lymphocytic leukemia, childhood L2", "pediatric acute lymphocytic leukemia, L2", "L2 lymphocytic leukemia, acute childhood", "L2 acute lymphocytic leukemia, childhood", "L2 childhood acute lymphoblastic leukemia", "Childhood L2 Acute Lymphoblastic Leukemia", "L2 lymphoblastic leukemia, acute childhood", "leukemia, childhood acute lymphocytic , L2", "pediatric acute lymphoblastic leukemia, L2", "childhood acute lymphoblastic leukemia, L2", "L2 acute lymphoblastic leukemia, childhood", "acute lymphoblastic leukemia, childhood L2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood L2 Acute Lymphoblastic Leukemia", "shortest_name_length": 16}
{"curie": "UMLS:C0266103", "names": ["NDC", "incisive canal cyst", "Incisive canal cyst", "cyst; incisive canal", "incisive canal; cyst", "Nasopalatine Duct Cyst", "nasopalatine duct cyst", "Nasopalatine duct cyst", "Naso-palatine duct cyst", "Cyst (of) incisive canal", "nasopalatine fissural cyst", "Median anterior maxillary cyst", "cyst; median anterior maxillary", "medial; cyst, anterior maxillary", "maxillary; cyst, median anterior", "Naso-palatine duct cyst (disorder)", "nasopalatine fissural cyst (diagnosis)", "median anterior maxillary fissural cyst", "median anterior maxillary fissural cyst (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Naso-palatine duct cyst", "shortest_name_length": 3}
{"curie": "MONDO:0008549", "names": ["thoracic dysostosis, isolated", "THORACIC DYSOSTOSIS, ISOLATED", "Thoracic Dysostosis, Isolated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thoracic dysostosis, isolated", "shortest_name_length": 29}
{"curie": "UMLS:C0334268", "names": ["Sinonasal papilloma", "Sinonasal Papilloma", "sinonasal papilloma", "schneiderian papilloma", "Schneiderian papilloma", "Schneiderian Papilloma", "Schneiderian papilloma, NOS", "Sinonasal Schneiderian Papilloma", "Benign inverted transitional papilloma", "Benign transitional papilloma, inverted", "Benign inverted transitional cell papilloma", "Benign transitional cell papilloma, inverted", "Benign inverted transitional cell papilloma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign inverted transitional cell papilloma", "shortest_name_length": 19}
{"curie": "MONDO:0009935", "names": ["PPH5", "PULMONARY HYPERTENSION, PRIMARY, 5", "Pulmonary Hypertension, Primary, Autosomal Recessive", "pulmonary hypertension, primary, autosomal recessive", "PULMONARY HYPERTENSION, PRIMARY, 5, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary hypertension, primary, autosomal recessive", "shortest_name_length": 4}
{"curie": "MONDO:0004251", "names": ["Small Bowel Tumor", "small bowel tumor", "Small Bowel Neoplasm", "small bowel neoplasm", "tumor of small bowel", "Tumor of Small Bowel", "Small Intestine Tumor", "small intestine tumor", "intestine small tumor", "Small intestine tumor", "intestine small tumors", "intestine small tumour", "intestines small tumor", "Small intestine tumour", "neoplasm of small bowel", "Neoplasm of Small Bowel", "intestines small tumors", "Small Intestine Neoplasm", "tumor of small intestine", "Tumor of small intestine", "tumor of the small bowel", "Tumor of the Small Bowel", "small intestine neoplasm", "Tumor of Small Intestine", "Small Intestinal Neoplasm", "Tumour of small intestine", "Small intestinal neoplasm", "small intestinal neoplasm", "Neoplasm of small intestine", "neoplasm of small intestine", "neoplasm of the small bowel", "Neoplasm of the Small Bowel", "Neoplasm of Small Intestine", "tumor of the small intestine", "Tumor of the Small Intestine", "Neoplasm of the small intestine", "Neoplasm of the Small Intestine", "small intestine benign neoplasm", "neoplasm of the small intestine", "small intestine neoplasm (disease)", "Neoplasm of small intestine (disorder)", "neoplasm of small intestine (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small intestine neoplasm", "shortest_name_length": 17}
{"curie": "UMLS:C4520728", "names": ["Stage IV Pediatric Hepatoma", "Stage IV Childhood Hepatoma", "Stage IV Hepatocellular Cancer", "stage IV childhood liver cancer", "Stage IV Pediatric Liver Cell Carcinoma", "Stage IV Childhood Liver Cell Carcinoma", "Stage IV Pediatric Hepatocellular Carcinoma", "Stage IV Childhood Hepatocellular Carcinoma", "Stage IV Childhood Hepatocellular Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Childhood Hepatocellular Carcinoma AJCC v7", "shortest_name_length": 27}
{"curie": "MONDO:0001896", "names": ["HYDROCEPHALY OBSTRUCTIVE", "Hydrocephaly obstructive", "HYDROCEPHALUS OBSTRUCTIVE", "Obstructive Hydrocephalus", "Obstructive hydrocephalus", "obstructive hydrocephalus", "Hydrocephalus, Obstructive", "HYDROCEPHALUS, OBSTRUCTIVE", "obstructive; hydrocephalus", "hydrocephalus; obstructive", "Noncommunicating hydrocephalus", "hydrocephalus; noncommunicating", "noncommunicating; hydrocephalus", "Non-communicating hydrocephalus", "non-communicating hydrocephalus", "HYDROCEPHALUS, NONCOMMUNICATING", "Non-Communicating Hydrocephalus", "Acquired obstructive hydrocephalus", "Obstructive hydrocephalus (disorder)", "obstructive hydrocephalus (diagnosis)", "Acquired obstructive hydrocephalus (disorder)", "obstructive hydrocephalus (increased pressure)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "obstructive hydrocephalus", "shortest_name_length": 24}
{"curie": "MONDO:0001051", "names": ["Tank ear", "tank ear", "Beach ear", "beach ear", "acute swimmers' ear", "Acute swimmers' ear", "acute swimmer's ear", "acute otitis externa", "Acute otitis externa", "OTITIS EXTERNA, ACUTE", "acute; otitis externa", "otitis externa, acute", "otitis; externa, acute", "Acute otitis externa NOS", "Acute otitis externa, NOS", "Acute otitis externa, diffuse", "acute otitis externa, diffuse", "Acute bacterial otitis externa", "otitis externa acute bacterial", "Acute otitis externa (disorder)", "acute otitis externa (diagnosis)", "Acute bacterial otitis externa (disorder)", "Acute bacterial otitis externa (diagnosis)", "acute bacterial inflammation of external ear", "Acute bacterial inflammation of external ear, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute otitis externa", "shortest_name_length": 8}
{"curie": "UMLS:C1335921", "names": ["Sarcoma by NCI Grade", "NCI Tumor Grade in Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sarcoma by NCI Grade", "shortest_name_length": 20}
{"curie": "UMLS:C1336482", "names": ["Stage I Small Cell Lung Cancer", "Stage I Small Cell Lung Carcinoma", "Stage I Small Cell Carcinoma of Lung", "Stage I Small Cell Carcinoma of the Lung", "Stage I Lung Small Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Lung Small Cell Carcinoma AJCC v7", "shortest_name_length": 30}
{"curie": "UMLS:C5555182", "names": ["Refractory Ovarian Clear Cell Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Ovarian Clear Cell Adenocarcinoma", "shortest_name_length": 44}
{"curie": "MONDO:0002503", "names": ["astrocytic tumor", "Astrocytic Tumor", "adult astrocytoma", "Adult Astrocytic Tumor", "adult astrocytic tumor", "adult astrocytic tumour", "Adult Astrocytic Tumour", "adult astrocytic tumors", "Adult Astrocytic Neoplasm", "adult astrocytic neoplasm", "Brain tumor, adult: Astrocytoma/Astrocytic tumors"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult astrocytic tumour", "shortest_name_length": 16}
{"curie": "MONDO:0008796", "names": ["Sommer Rathbun Battles syndrome", "Sommer-Rathbun-Battles syndrome", "Aniridia renal agenesis psychomotor retardation", "aniridia renal agenesis psychomotor retardation", "aniridia-renal agenesis-psychomotor retardation syndrome", "Aniridia-renal agenesis-psychomotor retardation syndrome", "aniridia, renal agenesis, psychomotor retardation syndrome", "Aniridia, renal agenesis, psychomotor retardation syndrome", "Aniridia, renal agenesis, psychomotor retardation syndrome (disorder)", "aniridia, renal agenesis, psychomotor retardation syndrome (diagnosis)", "Aniridia partial with unilateral renal agenesis and psychomotor retardation", "aniridia partial with unilateral renal agenesis and psychomotor retardation", "aniridia, partial, with unilateral renal agenesis and psychomotor retardation", "ANIRIDIA, PARTIAL, WITH UNILATERAL RENAL AGENESIS AND PSYCHOMOTOR RETARDATION", "Aniridia, Partial, with Unilateral Renal Agenesis and Psychomotor Retardation", "[OBSOLETE] Aniridia, Partial, with Unilateral Renal Agenesis and Psychomotor Retardation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aniridia-renal agenesis-psychomotor retardation syndrome", "shortest_name_length": 31}
{"curie": "MONDO:0019332", "names": ["PPKP1", "Buschke-Fischer-Brauer syndrome", "Brauer-Buschke-Fischer syndrome", "punctate palmoplantar keratoderma type 1", "type I punctate palmoplantar keratoderma", "punctate palmoplantar keratoderma type I", "keratoderma, palmoplantar punctate type 1", "keratodermia palmoplantaris papulosa, Buschke-Fischer-Brauer type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "punctate palmoplantar keratoderma type 1", "shortest_name_length": 5}
{"curie": "MONDO:0021966", "names": ["baker Vinters syndrome", "Baker Vinters syndrome", "Hydrocephalus with cerebral aqueductal dysgenesis and craniofacial anomalies", "hydrocephalus with cerebral aqueductal dysgenesis and craniofacial anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "baker Vinters syndrome", "shortest_name_length": 22}
{"curie": "MONDO:0014484", "names": ["MCPH12", "primary autosomal recessive microcephaly 12", "MICROCEPHALY 12, PRIMARY, AUTOSOMAL RECESSIVE", "microcephaly 12, primary, autosomal recessive", "CDK6 autosomal recessive primary microcephaly", "autosomal recessive primary microcephaly caused by mutation in CDK6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly 12, primary, autosomal recessive", "shortest_name_length": 6}
{"curie": "MONDO:0005190", "names": ["macroglobulinemia", "primary macroglobulinemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macroglobulinemia", "shortest_name_length": 17}
{"curie": "UMLS:C1333432", "names": ["EBV-Related Malignancy", "EBV Related Malignancy", "EBV-Related Malignant Neoplasm", "Epstein-Barr Virus Related Malignancy", "Epstein-Barr Virus-Related Malignancy", "Epstein-Barr Virus-Related Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "EBV-Related Malignant Neoplasm", "shortest_name_length": 22}
{"curie": "UMLS:C5401298", "names": ["NLS", "Naevus Lipomatosus Superficialis", "Naevus Lipomatosus Cutaneous Superficialis (of Hoffman-Zurhelle)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Naevus Lipomatosus Superficialis", "shortest_name_length": 3}
{"curie": "OMIM:610141", "names": ["QT INTERVAL, VARIATION IN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 25}
{"curie": "UMLS:C1333563", "names": ["FIGO Stage IV GTT", "FIGO Stage IV Gestational Trophoblastic Tumor", "FIGO Stage IV Gestational Trophoblastic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Stage IV Gestational Trophoblastic Tumor", "shortest_name_length": 17}
{"curie": "UMLS:C1709658", "names": ["Primary Cutaneous Intravascular Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Cutaneous Intravascular Large B-Cell Lymphoma", "shortest_name_length": 53}
{"curie": "MONDO:0024286", "names": ["benign vascular tumor", "benign blood vessel tumor", "Benign Blood Vessel Tumor", "benign blood vessel neoplasm", "Benign blood vessel neoplasm", "Benign Blood Vessel Neoplasm", "Benign neoplasm of blood vessel", "benign neoplasm of blood vessel", "Benign neoplasm of blood vessel, NOS", "Benign neoplasm of blood vessel (disorder)", "Benign blood vessel neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign blood vessel neoplasm", "shortest_name_length": 21}
{"curie": "UMLS:C1336323", "names": ["Stage II Supradiaphragmatic Hodgkin Lymphoma Lymphocyte Depleted", "Stage II Supradiaphragmatic Lymphocyte Depleted Hodgkin Lymphoma", "Stage II Supradiaphragmatic Hodgkin's Lymphoma Lymphocyte Depleted", "Stage II Supradiaphragmatic Lymphocyte Depleted Hodgkin's Lymphoma", "Stage II Supradiaphragmatic Hodgkin's Disease Lymphocyte Depletion Type", "Stage II Hodgkin's Disease Lymphocyte Depletion Type above the Diaphragm", "Stage II Hodgkin's Lymphoma Lymphocyte Depletion Type above the Diaphragm", "Stage II Supradiaphragmatic Lymphocyte Depleted Classical Hodgkin Lymphoma", "Stage II Supradiaphragmatic Lymphocyte-Depleted Classical Hodgkin Lymphoma", "Ann Arbor Stage II Supradiaphragmatic Lymphocyte-Depleted Classic Hodgkin Lymphoma", "Ann Arbor Stage II Supradiaphragmatic Lymphocyte-Depleted Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage II Supradiaphragmatic Lymphocyte-Depleted Classic Hodgkin Lymphoma", "shortest_name_length": 64}
{"curie": "MONDO:0010231", "names": ["MRX20", "XLID20", "X-linked mental retardation 20", "mental retardation, X-linked 20", "Mental Retardation, X-Linked 20", "MENTAL RETARDATION, X-LINKED 20", "intellectual disability, X-linked 20", "X-linked mental retardation 20 (MRX20, XLMR20)", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 20", "non-syndromic X-linked intellectual disability 20"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 20", "shortest_name_length": 5}
{"curie": "MONDO:0018893", "names": ["SAMS 1-31", "Cobb syndrome", "Cobb Syndrome", "Cobb's syndrome", "Cobb's Syndrome", "Cobb's syndrome (disorder)", "cutaneomeningospinal angiomatosis", "Cutaneomeningospinal angiomatosis", "spinal arteriovenous metameric syndrome", "Spinal arteriovenous metameric syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cobb syndrome", "shortest_name_length": 9}
{"curie": "UMLS:C1262146", "names": ["Renal salt-wasting syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal salt-wasting syndrome", "shortest_name_length": 27}
{"curie": "UMLS:C1704616", "names": ["Heart Rhabdomyosarcoma", "Cardiac Rhabdomyosarcoma", "cardiac rhabdomyosarcoma", "rhabdomyosarcoma of heart", "rhabdomyosarcoma of heart (diagnosis)", "malignant cardiac neoplasm rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiac Rhabdomyosarcoma", "shortest_name_length": 22}
{"curie": "UMLS:C0393684", "names": ["cingulate epilepsy", "Cingulate epilepsy", "Cingulate Epilepsy", "Epilepsy, Cingulate", "Cingulate Epilepsies", "Epilepsies, Cingulate", "Cingulate epilepsy (disorder)", "cingulate epilepsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epilepsy, Cingulate", "shortest_name_length": 18}
{"curie": "UMLS:C5204113", "names": ["Metastatic Pancreatic Ductal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Pancreatic Ductal Adenocarcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0014544", "names": ["OI16", "OI, type 16", "OI, TYPE XVI", "osteogenesis imperfecta type 16", "osteogenesis imperfecta, type 16", "osteogenesis imperfecta type XVI", "OSTEOGENESIS IMPERFECTA, TYPE XVI", "osteogenesis imperfecta, type XVI", "chromosome 11p11.2 deletion syndrome 91.3-KB", "CHROMOSOME 11p11.2 DELETION SYNDROME, 91.3-KB", "chromosome 11P11.2 deletion syndrome, 91.3-Kb"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteogenesis imperfecta type 16", "shortest_name_length": 4}
{"curie": "MONDO:0010438", "names": ["PNH1", "paroxysmal nocturnal hemoglobinuria 1", "PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 1", "PIGA paroxysmal nocturnal hemoglobinuria", "pIgA paroxysmal nocturnal hemoglobinuria", "paroxysmal nocturnal hemoglobinuria type 1", "paroxysmal nocturnal hemoglobinuria, somatic", "paroxysmal nocturnal hemoglobinuria caused by mutation in pIgA", "paroxysmal nocturnal hemoglobinuria caused by mutation in PIGA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paroxysmal nocturnal hemoglobinuria 1", "shortest_name_length": 4}
{"curie": "MONDO:0012060", "names": ["DFNB35", "autosomal recessive deafness 35", "DEAFNESS, AUTOSOMAL RECESSIVE 35", "deafness, autosomal recessive 35", "Deafness, Autosomal Recessive 35", "deafness, autosomal recessive type 35", "autosomal recessive nonsyndromic deafness 35", "ESRRB autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 35", "autosomal recessive nonsyndromic deafness type 35", "autosomal recessive nonsyndromic deafness caused by mutation in ESRRB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 35", "shortest_name_length": 6}
{"curie": "MONDO:0005523", "names": ["Steroid Metabolism, Inborn Errors", "Steroid Metabolic Diseases, Inborn", "Inborn Errors of Steroid Metabolism", "steroid inherited metabolic disorder", "Congenital Errors of Steroid Metabolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "steroid inherited metabolic disorder", "shortest_name_length": 33}
{"curie": "UMLS:C1336484", "names": ["Stage I Subdiaphragmatic Lymphocyte Depleted Hodgkin Lymphoma", "Stage I Subdiaphragmatic Hodgkin Lymphoma Lymphocyte Depleted", "Stage I Subdiaphragmatic Lymphocyte Depleted Hodgkin's Lymphoma", "Subdiaphragm Stage I Hodgkin's Lymphoma Lymphocyte Depletion Type", "Stage I Subdiaphragmatic Hodgkin's Disease Lymphocyte Depletion Type", "Stage I Subdiaphragmatic Lymphocyte-Depleted Classical Hodgkin Lymphoma", "Stage I Hodgkin's Disease Lymphocyte Depletion Type below the Diaphragm", "Stage I Subdiaphragmatic Lymphocyte Depleted Classical Hodgkin Lymphoma", "Stage I Hodgkin's Lymphoma Lymphocyte Depletion Type below the Diaphragm", "Ann Arbor Stage I Subdiaphragmatic Lymphocyte-Depleted Classic Hodgkin Lymphoma", "Ann Arbor Stage I Subdiaphragmatic Lymphocyte-Depleted Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage I Subdiaphragmatic Lymphocyte-Depleted Classic Hodgkin Lymphoma", "shortest_name_length": 61}
{"curie": "UMLS:C1880424", "names": ["Ductal carcinoma in situ, solid type", "Breast Ductal Carcinoma In Situ, Solid Type", "Ductal Breast Carcinoma in Situ, Solid Type", "Ductal Breast Carcinoma In Situ, Solid Type", "solid type ductal carcinoma in situ of breast", "solid type ductal carcinoma in situ of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "solid type ductal carcinoma in situ of breast", "shortest_name_length": 36}
{"curie": "MONDO:0001899", "names": ["Rheumatic heart failure", "rheumatic heart failure", "congestive rheumatic heart failure", "rheumatic congestive heart failure", "Rheumatic congestive heart failure", "Congestive rheumatic heart failure", "rheumatic heart failure (diagnosis)", "Rheumatic heart failure (congestive)", "rheumatic heart failure (congestive)", "Congestive rheumatic heart failure (disorder)", "congestive rheumatic heart failure (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rheumatic congestive heart failure", "shortest_name_length": 23}
{"curie": "UMLS:C0279083", "names": ["meningeal CGL", "meningeal CML", "CGL, meningeal", "CML, meningeal", "Meningeal Chronic Myelogenous Leukemia", "meningeal chronic myelogenous leukemia", "chronic myelocytic leukemia, meningeal", "myelocytic leukemia, meningeal chronic", "myelogenous leukemia, meningeal chronic", "chronic myelogenous leukemia, meningeal", "leukemia, meningeal chronic myelogenous", "granulocytic leukemia, meningeal chronic", "chronic granulocytic leukemia, meningeal", "Meningeal Chronic Myelogenous Leukemia, BCR-ABL1 Positive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meningeal Chronic Myelogenous Leukemia, BCR-ABL1 Positive", "shortest_name_length": 13}
{"curie": "UMLS:C0004616", "names": ["Fungal Aneurysm", "Aneurysm, Fungal", "Fungal Aneurysms", "mycotic aneurysm", "Mycotic aneurysm", "Aneurysm;mycotic", "Mycotic Aneurysm", "Aneurysm, Mycotic", "mycotic aneurysms", "aneurysm; mycotic", "ANEURYSM, MYCOTIC", "Aneurysms, Fungal", "Aneurysm, mycotic", "Mycotic Aneurysms", "mycotic; aneurysm", "Aneurysms, Mycotic", "Bacterial aneurysm", "Bacterial Aneurysm", "Aneurysm, Bacterial", "Bacterial Aneurysms", "Aneurysms, Bacterial", "Embolomycotic aneurysm", "Mycotic aneurysm (disorder)", "mycotic aneurysm (diagnosis)", "Mycotic aneurysm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aneurysm, Bacterial", "shortest_name_length": 15}
{"curie": "UMLS:C1334573", "names": ["Malignant Childhood CNS Tumor", "Malignant Pediatric CNS Tumor", "Childhood Malignant CNS Tumors", "Malignant Childhood CNS Neoplasm", "Malignant Pediatric Tumor of CNS", "Malignant Childhood Tumor of CNS", "Malignant Pediatric CNS Neoplasm", "Childhood Malignant CNS Neoplasms", "Malignant Pediatric Neoplasm of CNS", "Malignant Childhood Neoplasm of CNS", "Malignant Childhood Tumor of the CNS", "Malignant Pediatric Tumor of the CNS", "Malignant Pediatric Neoplasm of the CNS", "Malignant Childhood Neoplasm of the CNS", "Malignant Central Nervous System Neoplasm", "Malignant central nervous system neoplasm", "Malignant Pediatric Central Nervous System Tumor", "Malignant Childhood Central Nervous System Tumor", "Malignant Childhood Central Nervous System Tumors", "Childhood Malignant Central Nervous System Tumors", "Malignant Pediatric Central Nervous System Neoplasm", "Malignant Childhood Central Nervous System Neoplasm", "Malignant Pediatric Tumor of Central Nervous System", "Childhood Malignant Central Nervous System Neoplasm", "Malignant Childhood Tumor of Central Nervous System", "Malignant Childhood Central Nervous System Neoplasms", "Malignant Central Nervous System Tumors of Childhood", "Childhood Malignant Central Nervous System Neoplasms", "Malignant Childhood Neoplasm of Central Nervous System", "Malignant Pediatric Neoplasm of Central Nervous System", "Malignant Childhood Tumor of the Central Nervous System", "Malignant Central Nervous System Neoplasms of Childhood", "Malignant Pediatric Tumor of the Central Nervous System", "Malignant Pediatric Neoplasm of the Central Nervous System", "Malignant Childhood Neoplasm of the Central Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Malignant Central Nervous System Neoplasm", "shortest_name_length": 29}
{"curie": "UMLS:C1518709", "names": ["Ovarian Dermoid Cyst with Secondary Sebaceous Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Dermoid Cyst with Secondary Sebaceous Tumor", "shortest_name_length": 51}
{"curie": "UMLS:C0948075", "names": ["anal infection", "infection anus", "Anal Infection", "infection anal", "Anal infection", "anus infection", "anal infections", "anus; infection", "infection; anus", "anus infections", "Infection of anus", "Anal infection NOS", "Anal infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anal infection", "shortest_name_length": 14}
{"curie": "MONDO:0008722", "names": ["SCAD", "SCADD", "ACADSD", "SCAD deficiency", "Scad deficiency", "ACADS deficiency", "Scadh deficiency", "Acads deficiency", "short chain acyl-CoA dehydrogenase deficiency", "Short chain Acyl CoA dehydrogenase deficiency", "short-chain acyl-CoA dehydrogenase deficiency", "acyl-CoA dehydrogenase, short-chain deficiency", "Acyl-CoA Dehydrogenase, Short-Chain Deficiency", "acyl-CoA dehydrogenase, short-chain, deficiency OF", "Short-Chain Acyl-CoA Dehydrogenase Deficiency (SCAD)", "short-chain acyl-coenzyme A dehydrogenase deficiency", "short-chain acyl-CoA dehydrogenase deficiency (SCAD)", "short-chain acyl-Coenzyme A dehydrogenase deficiency (SCAD)", "Short-Chain Acyl-Coenzyme A Dehydrogenase Deficiency (SCAD)", "lipid-storage myopathy secondary to short-chain acyl-Coa dehydrogenase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short chain acyl-CoA dehydrogenase deficiency", "shortest_name_length": 4}
{"curie": "UMLS:C1517118", "names": ["Fallopian Tube Metaplastic Papillary Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fallopian Tube Metaplastic Papillary Tumor", "shortest_name_length": 42}
{"curie": "MONDO:0012066", "names": ["Atfb1", "ATFB1", "Atrial fibrillation, familial 1", "Atrial Fibrillation, Familial, 1", "ATRIAL FIBRILLATION, FAMILIAL, 1", "atrial fibrillation, familial, 1", "Autosomal dominant atrial fibrillation", "Atrial fibrillation, autosomal dominant", "ATRIAL FIBRILLATION, AUTOSOMAL DOMINANT", "atrial fibrillation, autosomal dominant", "ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial fibrillation, familial, 1", "shortest_name_length": 5}
{"curie": "MONDO:0045010", "names": ["glycoprotein metabolism disease", "metabolic disorder; glycoprotein", "Glycoprotein metabolism disorder", "glycoprotein; metabolic disorder", "Disorder of glycoprotein metabolism", "disorder of glycoprotein metabolism", "disorders of glycoprotein metabolism", "Disorders of glycoprotein metabolism", "glycoprotein metabolic process disease", "disorder of glycoprotein metabolic process", "Disorder of glycoprotein metabolism (disorder)", "disorders of glycoprotein metabolism (diagnosis)", "Disorder of glycoprotein metabolism, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycoprotein metabolism disease", "shortest_name_length": 31}
{"curie": "MONDO:0019292", "names": ["dermis elastic tissue disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermis elastic tissue disorder", "shortest_name_length": 30}
{"curie": "MONDO:0012720", "names": ["KRBSAPA", "Saposin A Deficiency", "saposin A deficiency", "SAPOSIN A DEFICIENCY", "Krabbe disease, atypical", "Krabbe disease due to saposin A deficiency", "Krabbe disease, atypical due to saposin A deficiency", "Krabbe disease, atypical, due to saposin A deficiency", "Krabbe Disease, Atypical, due to Saposin A Deficiency", "KRABBE DISEASE, ATYPICAL, DUE TO SAPOSIN A DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Krabbe disease due to saposin A deficiency", "shortest_name_length": 7}
{"curie": "UMLS:C1709867", "names": ["Rectosigmoid Mucinous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rectosigmoid Mucinous Adenocarcinoma", "shortest_name_length": 36}
{"curie": "UMLS:C1333867", "names": ["Grade 1 Colorectal Adenocarcinoma", "Grade I Colorectal Adenocarcinoma", "Low Grade Colorectal Adenocarcinoma", "Well Differentiated Colorectal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade 1 Colorectal Adenocarcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C2713394", "names": ["Haim Monk Syndrome", "Haim-Monk Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Haim-Monk Syndrome", "shortest_name_length": 18}
{"curie": "MONDO:0007497", "names": ["EAR ANTITRAGUS, TAG AT BASE OF", "ear antitragus, tag at base of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ear antitragus, tag at base of", "shortest_name_length": 30}
{"curie": "UMLS:C4086154", "names": ["Childhood Cerebral Ganglioneuroblastoma", "childhood cerebral ganglioneuroblastoma", "Central Nervous System Ganglioneuroblastoma", "childhood central nervous system ganglioneuroblastoma", "Childhood Central Nervous System Ganglioneuroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Central Nervous System Ganglioneuroblastoma", "shortest_name_length": 39}
{"curie": "MONDO:0016860", "names": ["FAP due to monosomy 5q22.2", "familial polyposis coli due to monosomy 5q22.2", "familial adenomatous polyposis due to del(5)(q22.2)", "familial adenomatous polyposis due to monosomy 5q22.2", "colorectal adenomatous polyposis due to monosomy 5q22.2", "familial adenomatous polyposis due to 5q22.2 microdeletion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial adenomatous polyposis due to 5q22.2 microdeletion", "shortest_name_length": 26}
{"curie": "UMLS:C0861429", "names": ["Recurrent Colon Adenocarcinoma", "Adenocarcinoma of colon recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma of colon recurrent", "shortest_name_length": 30}
{"curie": "MONDO:0021431", "names": ["SCC of Buccal Mucosa", "scc of buccal mucosa", "SCC of the Buccal Mucosa", "scc of the buccal mucosa", "Carcinoma of cheek mucosa", "carcinoma of buccal mucosa", "Carcinoma of buccal mucosa", "buccal mucosa squamous cell carcinoma", "Buccal Mucosa Squamous Cell Carcinoma", "Squamous cell carcinoma of buccal mucosa", "Squamous Cell Carcinoma of Buccal Mucosa", "squamous cell carcinoma of buccal mucosa", "Squamous Cell Carcinoma of the Buccal Mucosa", "squamous cell carcinoma of the buccal mucosa", "SCC - Squamous cell carcinoma of buccal mucosa", "Squamous cell carcinoma of buccal mucosa (disorder)", "Squamous cell carcinoma of buccal mucosa (diagnosis)", "oral cavity malignant carcinoma squamous cell of buccal mucosa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "squamous cell carcinoma of buccal mucosa", "shortest_name_length": 20}
{"curie": "MONDO:0021001", "names": ["HFE", "HFE1", "hemochromatosis", "HEMOCHROMATOSIS", "Hemochromatosis type 1", "hemochromatosis type 1", "HEMOCHROMATOSIS, TYPE 1", "classic hemochromatosis", "Haemochromatosis type 1", "hemochromatosis, type 1", "HFE related hemochromatosis", "C282Y/C282Y hemochromatosis", "HFE-related hemochromatosis", "HFE related haemochromatosis", "hfe hemochromatosis, modifier of", "primary hemochromatosis - type 1", "hereditary hemochromatosis type 1", "Hemochromatosis type 1 (disorder)", "HFE-Associated Hereditary Hemochromatosis", "HFE-associated hereditary hemochromatosis", "symptomatic form of hemochromatosis type 1", "symptomatic form of classic hemochromatosis", "primary hemochromatosis - type 1 (diagnosis)", "symptomatic form of HFE-related hereditary hemochromatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemochromatosis type 1", "shortest_name_length": 3}
{"curie": "MONDO:0008672", "names": ["WTSN", "watson syndrome", "WATSON SYNDROME", "Watson Syndrome", "Watson syndrome", "Syndrome, Watson", "syndrome watsons", "watson's syndrome", "Watson's syndrome", "cafe-Au-lait Spots with pulmonic stenosis", "Cafe au Lait Spots with Pulmonic Stenosis", "PULMONIC STENOSIS WITH CAFE-AU-LAIT SPOTS", "CAFE-AU-LAIT SPOTS WITH PULMONIC STENOSIS", "pulmonic stenosis with cafe-Au-lait Spots", "Pulmonic Stenosis with Cafe au Lait Spots", "Pulmonic Stenosis with Cafe-au-Lait Spots", "Cafe-au-Lait Spots with Pulmonic Stenosis", "Cafe-au-lait macules with pulmonary stenosis", "Café-au-lait macules with pulmonary stenosis", "pulmonic stenosis/cafe-au-lait spots syndrome", "Café-au-lait macules with pulmonary stenosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Watson syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0015584", "names": ["FIRES", "AERRPS", "DESC syndrome", "febrile infection-related epilepsy syndrome", "Febrile infection related epilepsy syndrome", "Febrile infection-related epilepsy syndrome", "Idiopathic catastrophic epileptic encephalopathy", "idiopathic catastrophic epileptic encephalopathy", "status epilepticus owing to presumed encephalitis", "Febrile infection related epilepsy syndrome (disorder)", "Devastating epileptic encephalopathy in school-aged children", "devastating epileptic encephalopathy in school-aged children", "acute encephalitis with refractory repetitive partial seizures", "Acute encephalitis with refractory repetitive partial seizures", "Acute encephalitis with refractory, repetitive partial seizures", "Severe refractory status epilepticus owing to presumed encephalitis", "severe refractory status epilepticus owing to presumed encephalitis", "fever-induced refractory epileptic encephalopathy in school-aged children", "Acute non-herpetic encephalitis with severe refractory status epilepticus", "Fever-induced refractory epileptic encephalopathy in school-aged children", "acute non-herpetic encephalitis with severe refractory status epilepticus", "DESC (devastating epileptic encephalopathy in school-aged children) syndrome", "FIRES - fever-induced refractory epileptic encephalopathy in school-aged children"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "febrile infection-related epilepsy syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0010384", "names": ["Hysp1", "HYSP1", "Hypospadias 1, X-Linked", "HYPOSPADIAS 1, X-LINKED", "hypospadias 1, X-linked", "hypospadias 1, X-linked, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypospadias 1, X-linked", "shortest_name_length": 5}
{"curie": "MONDO:0002006", "names": ["labyrinthitis serous", "Serous labyrinthitis", "serous labyrinthitis", "acute serous labyrinthitis", "Serous labyrinthitis (disorder)", "serous labyrinthitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "serous labyrinthitis", "shortest_name_length": 20}
{"curie": "MONDO:0004255", "names": ["WAT", "FATWO", "mesonephroma", "Mesonephroma", "Mesonephromas", "Wolffian tumor", "Wolffian Tumor", "Wolffian Adenoma", "Wolffian adenoma", "Mesonephroma, NOS", "Wolffian duct tumor", "Mesonephric Adenoma", "Mesonephric adenoma", "Wolffian Duct Tumor", "Mesonephroma, benign", "Wolffian Duct Adenoma", "Wolffian duct adenoma", "Wolffian Adnexal Tumor", "Wolffian adnexal tumor", "Wolffian Duct Neoplasm", "Wolffian Adnexal Neoplasm", "Retiform Wolffian Adenoma", "Wolffian adnexal neoplasm", "female adnexal tumor of probable Wolffian origin", "Female adnexal tumor of probable Wolffian origin", "Female Adnexal Tumor of Probable Wolffian Origin", "FATWO Female adnexal tumor of probable Wolffian origin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wolffian adnexal tumor", "shortest_name_length": 3}
{"curie": "UMLS:C0920193", "names": ["Photodermatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Photodermatosis", "shortest_name_length": 15}
{"curie": "MONDO:0019180", "names": ["hht", "HHT", "Weber-Osler", "Osler-Rendu", "ORW DISEASE", "Osler Disease", "osler's disease", "Osler's Disease", "Osler's disease", "OSLER WEBER RENDU", "rendu weber osler", "osler rendu weber", "rendu osler weber", "Rendu-Osler-Weber", "osler weber rendu", "Osler Rendu Disease", "Weber Osler Disease", "rendu osler disease", "Rendu-Osler disease", "Weber-Osler Disease", "Osler-Rendu Disease", "Weber Osler Syndrome", "Weber-Osler Syndrome", "Osler-Rendu-Weber disease", "Osler-Rendu-Weber Disease", "rendu-osler-weber disease", "rendu weber osler disease", "rendu osler weber disease", "disease osler weber rendu", "Rendu Osler Weber Disease", "Osler Rendu Weber Disease", "osler-weber-rendu disease", "Osler-Weber-Rendu disease", "Osler-Weber-Rendu Disease", "OSLER-RENDU-WEBER DISEASE", "osler weber rendu disease", "Rendu-Osler-Weber Disease", "disease rendu-osler-weber", "Rendu-Osler-Weber disease", "Osler-Rendu-Weber syndrome", "rendu-osler-weber syndrome", "rendu osler weber syndrome", "Osler-Weber-Rendu Syndrome", "osler weber rendu syndrome", "osler-weber-rendu syndrome", "Rendu-Osler-Weber syndrome", "RENDU OSLER WEBER SYNDROME", "osler rendu syndrome weber", "osler-rendu-weber syndrome", "OSLER-WEBER-RENDU SYNDROME", "Osler Weber Rendu Syndrome", "telangiectasia; hemorrhagic", "osler rendus syndrome weber", "hemorrhagic; telangiectasia", "hereditary hemorrhagic telangiectasia", "Hereditary hemorrhagic telangiectasia", "Hereditary Hemorrhagic Telangiectasia", "HEREDITARY HEMORRHAGIC TELANGIECTASIA", "telangiectasia, hereditary hemorrhagic", "Telangiectasia, Hereditary Hemorrhagic", "TELANGIECTASIA, HEREDITARY HEMORRHAGIC", "Hemorrhagic Telangiectasia, Hereditary", "Hereditary haemorrhagic telangiectasia", "Osler hemorrhagic telangiectasia syndrome", "Osler haemorrhagic telangiectasia syndrome", "HHT - Hereditary hemorrhagic telangiectasia", "Osler's hemorrhagic telangiectasia syndrome", "HHT - Hereditary haemorrhagic telangiectasia", "hereditary hemorrhagic telangiectasia (diagnosis)", "Osler hemorrhagic telangiectasia syndrome (disorder)", "telangiectasia, hereditary Hemorrahagic, of Rendu, Osler", "Telangiectasia, Hereditary Hemorrahagic, of Rendu, Osler", "hereditary hemorrhagic telangiectasia (Osler-Rendu-Weber)", "Telangiectasia, Hereditary Hemorrhagic, of Rendu, Osler, and Weber", "TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary hemorrhagic telangiectasia", "shortest_name_length": 3}
{"curie": "MONDO:0011125", "names": ["TTD1", "TTDP", "TAY SYNDROME", "Tay syndrome", "PIBIDS Syndrome", "PIBIDS SYNDROME", "PIBIDS syndrome", "PIBIDS Syndromes", "Photosensitive Trichothiodystrophy", "Trichothiodystrophy, Photosensitive", "trichothiodystrophy, photosensitive", "TRICHOTHIODYSTROPHY, PHOTOSENSITIVE", "photosensitive trichothiodystrophy 1", "Photosensitive Trichothiodystrophies", "trichothiodystrophy 1, photosensitive", "Trichothiodystrophy 1, Photosensitive", "Trichothiodystrophies, Photosensitive", "TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE", "TRICHOTHIODYSTROPHY WITH CONGENITAL ICHTHYOSIS", "Trichothiodystrophy with Congenital Ichthyosis", "trichothiodystrophy with congenital ichthyosis", "Ichthyosis, Congenital, with Trichothiodystrophy", "ICHTHYOSIS, CONGENITAL, WITH TRICHOTHIODYSTROPHY", "ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH RETARDATION", "ichthyosiform erythroderma with hair Abnormality and mental and Growth retardation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichothiodystrophy 1, photosensitive", "shortest_name_length": 4}
{"curie": "MONDO:0019460", "names": ["BAL", "hybrid acute leukemia", "Hybrid acute leukemia", "ALL with myeloid markers", "AML with lymphoid markers", "biphenotypic acute leukemia", "Mixed lineage acute leukemia", "mixed lineage acute leukemia", "mixed phenotype acute leukemia", "leukemia acute ambiguous lineage", "acute leukemia of ambiguous lineage", "Acute leukemia of ambiguous lineage", "Acute Leukemia of Ambiguous Lineage", "acute leukemias of ambiguous lineage", "Acute leukaemia of ambiguous lineage", "acute leukemia of undetermined lineage", "Acute Leukemia of Indeterminate Lineage", "acute leukemia of indeterminate lineage", "Acute leukemia of indeterminate lineage", "Acute Leukemia of Ambiguous Lineage (ALAL)", "Acute leukemia of ambiguous lineage (disorder)", "Acute leukemia of ambiguous lineage (diagnosis)", "Acute Leukemia, ambiguous lineage (mixed or biphenotypic)", "Acute leukemia of ambiguous lineage (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute leukemia of ambiguous lineage", "shortest_name_length": 3}
{"curie": "UMLS:C1706980", "names": ["Bone Leiomyoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone Leiomyoma", "shortest_name_length": 14}
{"curie": "MONDO:0044347", "names": ["erythrocyte disease", "erythrocyte disorder", "disease of erythrocyte", "red blood cell disease", "red blood cell disorder", "Red blood cell disorder", "disorder of erythrocyte", "Red blood cell disorders", "red cell blood disorders", "red blood cell disorders", "blood cells disorder red", "RED BLOOD CELL DISORDERS", "blood cell disorders red", "blood cells disorders red", "Red blood cell disorder, NOS", "erythrocyte disease or disorder", "Red blood cell disorder (disorder)", "disease or disorder of erythrocyte", "red blood cell disorder (diagnosis)", "RED BLOOD CELL DISORDERS: GENERAL TERMS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythrocyte disorder", "shortest_name_length": 19}
{"curie": "MONDO:0010685", "names": ["MYP1", "Myopia 1", "Myopia, X-Linked", "MYOPIA 1, X-LINKED", "myopia 1, X-linked", "myopia-1, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopia 1, X-linked", "shortest_name_length": 4}
{"curie": "MONDO:0004052", "names": ["Rectal Cloacogenic Carcinoma", "rectal cloacogenic carcinoma", "cloacogenic carcinoma of rectum", "Cloacogenic Carcinoma of Rectum", "rectal transition zone carcinoma", "Rectal Transition Zone Carcinoma", "rectal transitional zone carcinoma", "Rectal Transitional Zone Carcinoma", "cloacogenic carcinoma of the rectum", "Transition Zone Carcinoma of Rectum", "transition zone carcinoma of rectum", "Cloacogenic Carcinoma of the Rectum", "transitional zone carcinoma of rectum", "transitional Zone carcinoma of rectum", "Transitional Zone Carcinoma of Rectum", "Transition Zone Carcinoma of the Rectum", "transition zone carcinoma of the rectum", "Transitional Zone Carcinoma of the Rectum", "transitional zone carcinoma of the rectum", "cloacogenic carcinoma of rectum (diagnosis)", "rectal neoplasm malignant carcinoma cloacogenic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rectal cloacogenic carcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0002880", "names": ["ovary adenosarcoma", "ovarian adenosarcoma", "Ovarian Adenosarcoma", "adenosarcoma of ovary", "Ovarian Müllerian Adenosarcoma", "ovarian Mullerian adenosarcoma", "Ovarian mullerian Adenosarcoma", "ovarian Müllerian adenosarcoma", "Ovarian Mullerian Adenosarcoma", "ovarian mullerian adenosarcoma", "ovarian mesodermal adenosarcoma", "Ovarian Mesodermal Adenosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian adenosarcoma", "shortest_name_length": 18}
{"curie": "MONDO:0035290", "names": ["aHUS with complement gene abnormality", "Atypical HUS with complement gene abnormality", "atypical hemolytic uremic syndrome with complement gene abnormality"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical hemolytic uremic syndrome with complement gene abnormality", "shortest_name_length": 37}
{"curie": "UMLS:C1337015", "names": ["Well Differentiated Fibrosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Well Differentiated Fibrosarcoma", "shortest_name_length": 32}
{"curie": "MONDO:0020419", "names": ["PAH", "a.pulmonalis; hypoplasia", "Underdeveloped lung artery", "Pulmonary artery hypoplasia", "pulmonary artery hypoplasia", "hypoplasia; pulmonary artery", "Hypoplasia of pulmonary artery", "hypoplasia of pulmonary artery", "Underdeveloped pulmonary artery", "pulmonary artery hypoplasia (disease)", "Unilateral Pulmonary Artery Hypoplasia", "Congenital hypoplasia of pulmonary artery", "hypoplasia of pulmonary artery (diagnosis)", "Congenital hypoplasia of pulmonary artery (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary artery hypoplasia", "shortest_name_length": 3}
{"curie": "MONDO:0006343", "names": ["ovarian transitional cell cancer", "Ovarian Transitional Cell Cancer", "ovary transitional cell carcinoma", "ovarian transitional cell neoplasm", "Ovarian Transitional Cell Carcinoma", "ovarian transitional cell carcinoma", "transitional cell carcinoma of ovary", "transitional cell carcinoma of Ovary", "Transitional Cell Carcinoma of Ovary", "Transitional Cell Carcinoma of the Ovary", "transitional cell carcinoma of the ovary", "malignant ovarian transitional cell neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian transitional cell carcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C0854845", "names": ["Intestinal T-cell lymphoma stage I", "Stage I Intestinal T-Cell Lymphoma", "Intestinal T-Cell Lymphoma Stage I", "Stage I Enteropathy-type T-Cell Lymphoma", "Stage I Enteropathy-Associated T-Cell Lymphoma", "Ann Arbor Stage I Enteropathy-Associated T-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal T-cell lymphoma stage I", "shortest_name_length": 34}
{"curie": "MONDO:0005999", "names": ["TB empyema", "Tuberculous Empyema", "Tuberculous empyema", "tuberculous empyema", "Empyema, Tuberculous", "Tuberculous Empyemas", "empyema; tuberculous", "tuberculosis; empyema", "Empyemas, Tuberculous", "Tuberculous pleural empyema", "Empyema, Pleural, Tuberculous", "tuberculous empyema of pleura", "Tuberculous empyema (disorder)", "tuberculous empyema (& pleural)", "tuberculous empyema of pleura (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tuberculous empyema", "shortest_name_length": 10}
{"curie": "MONDO:0003578", "names": ["extragonadal primary Nonseminoma", "Extragonadal Primary Nonseminoma", "malignant extragonadal Nonseminoma", "Malignant Extragonadal Nonseminoma", "Primary Malignant Extragonadal Nonseminoma", "primary malignant Extragonadal Nonseminoma", "primary malignant extragonadal Nonseminoma", "extragonadal nonseminomatous germ cell tumor", "extragonadal non-seminomatous germ cell cancer", "Extragonadal Non-Seminomatous Germ Cell Cancer", "cancer of extragonadal non-seminomatous germ cell", "Cancer of Extragonadal Non-Seminomatous Germ Cell", "cancer of the extragonadal non-seminomatous germ cell", "Cancer of the Extragonadal Non-Seminomatous Germ Cell", "malignant extragonadal nonseminomatous germ cell tumor", "malignant extragonadal non-seminomatous germ cell tumor", "Malignant Extragonadal Nongerminomatous Germ Cell Tumor", "Malignant Extragonadal Non-Seminomatous Germ Cell Tumor", "malignant extragonadal non-seminomatous germ cell neoplasm", "malignant tumor of extragonadal non-seminomatous germ cell", "Malignant Tumor of Extragonadal Non-Seminomatous Germ Cell", "Malignant Extragonadal Non-Seminomatous Germ Cell Neoplasm", "Malignant Neoplasm of Extragonadal Non-Seminomatous Germ Cell", "malignant neoplasm of extragonadal non-seminomatous germ cell", "Malignant Tumor of the Extragonadal Non-Seminomatous Germ Cell", "malignant tumor of the extragonadal non-seminomatous germ cell", "Malignant Neoplasm of the Extragonadal Non-Seminomatous Germ Cell", "malignant neoplasm of the extragonadal non-seminomatous germ cell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extragonadal nonseminomatous germ cell tumor", "shortest_name_length": 32}
{"curie": "MONDO:0006373", "names": ["PTAD", "PitNET", "PitNET/Adenoma", "Pituitary Adenoma", "pituitary adenoma", "PITUITARY ADENOMA", "Adenoma;pituitary", "Pituitary adenoma", "adenoma pituitary", "Pituitary Adenomas", "adenomas pituitary", "Adenoma, Pituitary", "Adenomas, Pituitary", "Adenoma of Pituitary", "Adenoma of pituitary", "adenoma of pituitary", "Pituitary adenoma, NOS", "Pituitary gland adenoma", "pituitary gland adenoma", "Pituitary Gland Adenoma", "adenoma of the pituitary", "Adenoma of the Pituitary", "Adenoma of Pituitary Gland", "adenoma of pituitary gland", "Pituitary adenoma (disorder)", "pituitary adenoma (diagnosis)", "adenoma of the pituitary gland", "Adenoma of the Pituitary Gland", "Pituitary Neuroendocrine Tumor", "adenoma of the Pituitary gland", "Noncancerous tumor in pituitary gland", "Pituitary Neuroendocrine Tumor/Adenoma", "Noncancerous tumour in pituitary gland", "ADENOMA, ANTERIOR LOBE PITUITARY GLAND, BENIGN", "adenoma, anterior lobe pituitary gland, benign", "Pituitary Neuroendocrine Tumor (Formerly Pituitary Adenoma)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pituitary gland adenoma", "shortest_name_length": 4}
{"curie": "MONDO:0030785", "names": ["MRT75", "autosomal recessive intellectual developmental disorder 75", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 75, WITH NEUROPSYCHIATRIC FEATURES AND VARIANT LISSENCEPHALY", "intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly", "shortest_name_length": 5}
{"curie": "MONDO:0044629", "names": ["amyoplasia congenita", "congenital amyoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital amyoplasia", "shortest_name_length": 20}
{"curie": "UMLS:C0282193", "names": ["iron excess", "Iron excess", "excess iron", "IRON OVERLOAD", "overload iron", "Iron overload", "Iron Overload", "excesses iron", "iron overload", "Overload, Iron", "iron overloading", "Iron overload, NOS", "iron overload disorder", "Increased storage iron", "Iron overload (disorder)", "iron overload (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Iron Overload", "shortest_name_length": 11}
{"curie": "MONDO:0033644", "names": ["MRCS1", "MICROCORNEA, ROD-CONE DYSTROPHY, CATARACT, AND POSTERIOR STAPHYLOMA 1", "microcornea, rod-cone dystrophy, cataract, and posterior staphyloma 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcornea, rod-cone dystrophy, cataract, and posterior staphyloma 1", "shortest_name_length": 5}
{"curie": "UMLS:C0235680", "names": ["Vaginitis ulcerative", "VAGINITIS ULCERATIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginitis ulcerative", "shortest_name_length": 20}
{"curie": "UMLS:C1706997", "names": ["Breakdown of Optical Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breakdown of Optical Tissue", "shortest_name_length": 27}
{"curie": "MONDO:0016677", "names": ["Drug-Induced Abnormality", "Abnormality, Drug-Induced", "Drug-Induced Abnormalities", "Drug Induced Abnormalities", "Abnormalities, Drug Induced", "Abnormalities, Drug-Induced", "toxic or drug-related embryofetopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "toxic or drug-related embryofetopathy", "shortest_name_length": 24}
{"curie": "MONDO:0010750", "names": ["Van De Berghe Dequeker syndrome", "van den Berghe Dequeker syndrome", "Van den Berghe-Dequecker syndrome", "ulnar hypoplasia-split foot syndrome", "severe ulnar aplasia and lobster claw feet", "Severe ulnar aplasia and lobster claw feet", "ulnar hypoplasia lobster claw deformity of feet", "Ulnar hypoplasia lobster claw deformity of feet", "familial ulnar aplasia and lobster claw syndrome", "Familial ulnar aplasia and lobster claw syndrome", "ULNAR HYPOPLASIA WITH LOBSTER-CLAW DEFORMITY OF FEET", "Ulnar Hypoplasia with Lobster-Claw Deformity of Feet", "ulnar hypoplasia with lobster-claw deformity of feet", "ulnar hypoplasia-lobster-claw deformity of feet syndrome", "complete absence of the ulna and of fingers 2 to 5, together with lobster-claw deformity of the feet"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ulnar hypoplasia-split foot syndrome", "shortest_name_length": 31}
{"curie": "MONDO:0014097", "names": ["CSBS", "Congenital Short Bowel Syndrome", "Congenital short bowel syndrome", "CONGENITAL SHORT BOWEL SYNDROME", "congenital short bowel syndrome", "Congenital short bowel syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital short bowel syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0100238", "names": ["inherited Fanconi renotubular syndrome", "hereditary Fanconi renotubular syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited Fanconi renotubular syndrome", "shortest_name_length": 38}
{"curie": "MONDO:0008749", "names": ["Php2", "PHP2", "Php 2", "Php Ii", "PHP II", "Pseudohypoparathyroidism type 2", "pseudohypoparathyroidism type 2", "Pseudohypoparathyroidism Type 2", "Pseudohypoparathyroidism, Type 2", "Pseudohypoparathyroidism type II", "PSEUDOHYPOPARATHYROIDISM, TYPE II", "pseudohypoparathyroidism, type II", "Pseudohypoparathyroidism, Type Ii", "Acquired Parathyroid Hormone Resistance", "Secondary Parathyroid Hormone Resistance", "Pseudohypoparathyroidism type II (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudohypoparathyroidism type 2", "shortest_name_length": 4}
{"curie": "MONDO:0016396", "names": ["PCH1", "MRT32", "PCH1A", "Norman disease", "Pontocerebellar hypoplasia type 1", "pontocerebellar hypoplasia type 1", "Pontocerebellar Hypoplasia Type 1", "Pontocerebellar Hypoplasia, Type 1a", "PONTOCEREBELLAR HYPOPLASIA, TYPE 1A", "PCH1 - pontocerebellar hypoplasia type 1", "mental retardation, autosomal recessive 32", "Congenital pontocerebellar hypoplasia type 1", "Congenital pontocerebellar hypoplasia type 1 (disorder)", "PONTOCEREBELLAR HYPOPLASIA WITH ANTERIOR HORN CELL DISEASE", "Pontocerebellar Hypoplasia With Anterior Horn Cell Disease", "pontocerebellar hypoplasia with anterior horn cell disease", "pontocerebellar hypoplasia with infantile spinal muscular atrophy", "PONTOCEREBELLAR HYPOPLASIA WITH INFANTILE SPINAL MUSCULAR ATROPHY", "Pontocerebellar Hypoplasia With Infantile Spinal Muscular Atrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pontocerebellar hypoplasia type 1", "shortest_name_length": 4}
{"curie": "UMLS:C1306600", "names": ["radial nerve palsy", "nerve palsy radial", "Radial nerve palsy", "RADIAL NERVE PALSY", "radial nerve palsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radial nerve palsy", "shortest_name_length": 18}
{"curie": "MONDO:0030038", "names": ["GLCC", "glaucoma, primary closed-angle", "GLAUCOMA, PRIMARY CLOSED-ANGLE", "GLAUCOMA, PRIMARY CLOSED ANGLE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glaucoma, primary closed-angle", "shortest_name_length": 4}
{"curie": "UMLS:C0266771", "names": ["placenta marginal", "Marginal Placenta", "Marginal placenta", "marginal placenta", "Placenta marginata", "Placenta, marginal", "Placenta Marginalis", "Placenta marginalis", "Circummarginate Placenta", "Placenta circummarginata", "Placenta circummarginate", "circummarginate placenta", "Placenta circummarginate (disorder)", "circummarginate placenta (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Placenta circummarginate", "shortest_name_length": 17}
{"curie": "MONDO:0013540", "names": ["Emberger syndrome", "Emberger Syndrome", "EMBERGER SYNDROME", "Emberger syndrome (disorder)", "Emberger syndrome (diagnosis)", "Deafness-lymphedema-leukemia syndrome", "deafness-lymphedema-leukemia syndrome", "Primary Lymphedema with Myelodysplasia", "lymphedema, primary, with myelodysplasia", "LYMPHEDEMA, PRIMARY, WITH MYELODYSPLASIA", "Deafness - lymphedema - leukemia syndrome", "Hearing loss-lymphedema-leukemia syndrome", "Deafness - lymphoedema - leukaemia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness-lymphedema-leukemia syndrome", "shortest_name_length": 17}
{"curie": "UMLS:C0271154", "names": ["Aphakic glaucoma", "Glaucoma, aphakic eye", "Aphakic glaucoma (diagnosis)", "Secondary glaucoma due to aphakia", "Secondary glaucoma due to aphakia (disorder)", "glaucoma associated with lens disorder aphakic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aphakic glaucoma", "shortest_name_length": 16}
{"curie": "MONDO:0029138", "names": ["DEE67", "EIEE67", "early infantile epileptic encephalopathy 67", "developmental and epileptic encephalopathy 67", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 67", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 67", "epileptic encephalopathy, early infantile, 67", "developmental and epileptic encephalopathy, 67"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 67", "shortest_name_length": 5}
{"curie": "MONDO:0008231", "names": ["Peyronie", "Penile plaque", "penile fibrosis", "disease peyronie", "peyronie disease", "PEYRONIE DISEASE", "Peyronie Disease", "Peyronie disease", "FIBROSIS, PENILE", "PENILE INDURATION", "diseases peyronie", "Disease;Peyronies", "Penile Induration", "Peyronies disease", "Peyronies Disease", "Penile induration", "peyronies disease", "penile induration", "PEYRONIES DISEASE", "disease peyronie's", "peyronie's disease", "Fibrous Cavernitis", "Peyronie's disease", "penile; induration", "Fibrous cavernitis", "PEYRONIE'S DISEASE", "diseases peyronies", "induration; penile", "Peyronie's Disease", "Penile fibromatosis", "Cavernitis, Fibrous", "Penile Fibromatosis", "PEYRONIE'S SYNDROME", "Fibrous cavernositis", "FIBROMATOSIS, PENILE", "Fibrous Cavernitides", "Fibromatosis, Penile", "Cavernitides, Fibrous", "Peyronie's Fibromatosis", "Peyronie's fibromatosis", "induratio penis plastica", "Induratio penis plastica", "Indurated penis plastica", "Plastic induration of penis", "Peyronie's disease (diagnosis)", "Plastic Induration of the Penis", "Induratio penis plastica (disorder)", "CORPORA CAVERNOSA, PLASTIC INDURATION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peyronie disease", "shortest_name_length": 8}
{"curie": "MONDO:0021420", "names": ["VOCAL CORD POLYP", "Vocal Cord Polyp", "Vocal cord polyp", "vocal cord polyp", "Vocal fold polyp", "polyps cord vocal", "polyps vocal cord", "vocal cord polyps", "fold polyps vocal", "cord polyps vocal", "polyp; vocal cord", "vocal cord; polyp", "cords polyp vocal", "cords polyps vocal", "Polyp(s);vocal cord", "Polyp of Vocal Cord", "Polyp of vocal cord", "polyp of vocal cord", "polyp of the vocal cord", "Polyp of the Vocal Cord", "laryngeal vocal fold polyp", "vocal cord polyp (diagnosis)", "Polyp of vocal cord (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyp of vocal cord", "shortest_name_length": 16}
{"curie": "MONDO:0054696", "names": ["IMD53", "immunodeficiency 53", "IMMUNODEFICIENCY 53"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 53", "shortest_name_length": 5}
{"curie": "MONDO:0003924", "names": ["ADENOMA ADRENAL", "adenoma adrenal", "Adenoma;adrenal", "Adrenal adenoma", "ADRENAL ADENOMA", "Adenoma adrenal", "adrenal adenoma", "Adrenal Adenoma", "adenomas adrenal", "adenoma; adrenal", "adrenal; adenoma", "adrenal gland adenoma", "adrenal incidentaloma", "Cortical Cell Adenoma", "cortical cell adenoma", "Adrenal Gland Adenoma", "adrenocortical adenoma", "Benign Adrenal Adenoma", "benign adrenal adenoma", "Adrenocortical adenoma", "Adrenal Cortex Adenoma", "adrenal cortex adenoma", "adenoma adrenal cortex", "BENIGN ADRENAL ADENOMA", "Adrenocortical Adenoma", "Adrenocortical Adenomas", "Adrenocortical adenomas", "ADRENAL CORTEX, ADENOMA", "Adenoma, Adrenocortical", "Adenoma of Adrenal Gland", "adenoma of adrenal gland", "Adrenal Cortical Adenoma", "adrenal cortical adenoma", "adenoma adrenal cortical", "Adrenal cortical adenoma", "Adenomas, Adrenocortical", "Adrenal Cortical Adenomas", "Adenoma of Adrenal Cortex", "Adenoma, Adrenal Cortical", "adenoma of adrenal cortex", "Adenomas, Adrenal Cortical", "Adrenal adenoma (disorder)", "adenoma of the Adrenal gland", "Adenoma of the Adrenal Gland", "adenoma of the adrenal gland", "Adrenal cortical adenoma NOS", "Benign Adrenal Gland Adenoma", "benign adrenal gland adenoma", "Adrenal cortical adenoma, NOS", "adenoma of the adrenal cortex", "Benign adrenal cortical tumor", "Adenoma of the Adrenal Cortex", "Benign adrenal cortical tumour", "Benign Adenoma of Adrenal Gland", "ADENOMA, ADRENOCORTICAL, BENIGN", "Benign adrenal cortical adenoma", "benign adenoma of adrenal gland", "adenoma, adrenocortical, benign", "benign adenoma of the adrenal gland", "Adrenal cortical adenoma (disorder)", "Benign Adenoma of the Adrenal Gland", "adrenal cortical adenoma (diagnosis)", "adenoma of adrenal gland (diagnosis)", "Adrenal cortical adenoma - morphology", "Benign adrenal cortical adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adrenal cortex adenoma", "shortest_name_length": 15}
{"curie": "MONDO:0006105", "names": ["Benign Conjunctiva Tumor", "benign conjunctiva tumor", "Benign Conjunctival Tumor", "benign conjunctival tumor", "benign conjunctiva neoplasm", "Benign Tumor of Conjunctiva", "Benign tumor of conjunctiva", "conjunctiva benign neoplasm", "benign tumor of conjunctiva", "Benign Conjunctiva Neoplasm", "Benign Conjunctival Neoplasm", "benign conjunctival neoplasm", "Benign tumour of conjunctiva", "benign neoplasm of conjunctiva", "Benign Neoplasm of Conjunctiva", "Benign neoplasm of conjunctiva", "benign tumor of the conjunctiva", "Benign Tumor of the Conjunctiva", "benign neoplasm of the conjunctiva", "Benign Neoplasm of the Conjunctiva", "Benign neoplasm of conjunctiva (disorder)", "benign neoplasm of conjunctiva (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign conjunctival neoplasm", "shortest_name_length": 24}
{"curie": "MONDO:0017922", "names": ["deafness-onychodystrophy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness-onychodystrophy syndrome", "shortest_name_length": 33}
{"curie": "UMLS:C3274484", "names": ["Congenital Abnormality of the Large Intestine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Abnormality of the Large Intestine", "shortest_name_length": 45}
{"curie": "MONDO:0800141", "names": ["MAN2B2 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MAN2B2 deficiency", "shortest_name_length": 17}
{"curie": "UMLS:C4526753", "names": ["Refractory Diffuse Intrinsic Pontine Glioma", "Refractory Diffuse Intrinsic Pontine Glioma (DIPG)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Diffuse Intrinsic Pontine Glioma", "shortest_name_length": 43}
{"curie": "MONDO:0007881", "names": ["STHAG4", "WNT10A tooth agenesis", "TOOTH AGENESIS, SELECTIVE 4", "Lateral Incisors, Absence of", "lateral incisors, absence of", "TOOTH AGENESIS, SELECTIVE, 4", "Tooth Agenesis, Selective, 4", "tooth agenesis, selective, 4", "LATERAL INCISORS, ABSENCE OF", "Succedaneous Teeth, Agenesis Of", "succedaneous teeth, agenesis of", "SUCCEDANEOUS TEETH, AGENESIS OF", "tooth agenesis, selective, type 4", "Lateral Incisors, Pegged or Missing", "lateral incisors, pegged or missing", "LATERAL INCISORS, PEGGED OR MISSING", "TOOTH AGENESIS, SELECTIVE, 4 (disorder)", "tooth agenesis caused by mutation in WNT10A", "TOOTH AGENESIS, SELECTIVE, 4, WITH OR WITHOUT ECTODERMAL DYSPLASIA", "tooth agenesis, selective, 4, with or without ectodermal dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tooth agenesis, selective, 4", "shortest_name_length": 6}
{"curie": "MONDO:0006189", "names": ["porocarcinoma", "Porocarcinoma", "Eccrine Porocarcinoma", "Eccrine porocarcinoma", "eccrine porocarcinoma", "Eccrine Porocarcinomas", "Porocarcinoma, Eccrine", "Porocarcinomas, Eccrine", "malignant eccrine poroma", "malignant Eccrine Poroma", "Malignant Eccrine Poroma", "Eccrine Poroma, Malignant", "Eccrine poroma, malignant", "Malignant Eccrine Poromas", "Poroma, Malignant Eccrine", "Eccrine Poromas, Malignant", "Poromas, Malignant Eccrine", "Eccrine porocarcinoma of skin", "eccrine porocarcinoma of skin", "Epidermotropic Eccrine Carcinoma", "epidermotropic eccrine carcinoma", "porocarcinoma/spiroadenocarcinoma", "Eccrine porocarcinoma of skin (disorder)", "Eccrine porocarcinoma of skin (diagnosis)", "Eccrine poroma, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eccrine porocarcinoma", "shortest_name_length": 13}
{"curie": "MONDO:0006394", "names": ["rectal tubular adenoma", "Rectal Tubular Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rectal tubular adenoma", "shortest_name_length": 22}
{"curie": "UMLS:C0855060", "names": ["Localized Liposarcoma", "Liposarcoma Nonmetastatic", "Non-Metastatic Liposarcoma", "Liposarcoma non-metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liposarcoma non-metastatic", "shortest_name_length": 21}
{"curie": "UMLS:C5420328", "names": ["Lymphoepithelial Sialadenitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoepithelial Sialadenitis", "shortest_name_length": 29}
{"curie": "UMLS:C4683421", "names": ["Stage IV Differentiated Thyroid Gland Cancer", "Stage IV Differentiated Thyroid Gland Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Differentiated Thyroid Gland Carcinoma AJCC v8", "shortest_name_length": 44}
{"curie": "MONDO:0012521", "names": ["HSE", "HSVE", "ENCEPHALITIS HSV", "hsv encephalitis", "encephalitis hsv", "HSV encephalitis", "Encephalitis herpes", "Herpes encephalitis", "herpes encephalitis", "encephalitis herpes", "Herpes Encephalitis", "Encephalitis, Herpes", "ENCEPHALITIS, HERPES", "HERPETIC ENCEPHALITIS", "Herpetic Encephalitis", "Herpetic encephalitis", "herpetic encephalitis", "Encephalitis, Herpetic", "Herpetic Encephalitides", "Encephalitides, Herpetic", "Herpesviral encephalitis", "HEMMORRHAGIC ENCEPHALITIS", "Herpes simplex encephalitis", "HERPES SIMPLEX ENCEPHALITIS", "herpes simplex encephalitis", "Herpes Simplex Encephalitis", "Herpes simplex neuroinvasion", "Encephalitis, Herpes Simplex", "Herpes Simplex Encephalitides", "Encephalitides, Herpes Simplex", "Encephalitis due to Herpesvirus", "Encephalitis due to Herpesviridae", "Herpes simplex virus encephalitis", "HSE - Herpes simplex encephalitis", "Encephalitis caused by Herpesvirus", "Herpes simplex meningo-encephalitis", "Simplexvirus infectious encephalitis", "Encephalitis caused by Herpesviridae", "STRUMPELL-LEICHTENSTERN ENCEPHALITIS", "Herpes simplex encephalitis (diagnosis)", "Simplexvirus caused infectious encephalitis", "Encephalitis caused by Herpesvirus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "herpes simplex encephalitis", "shortest_name_length": 3}
{"curie": "MONDO:0009959", "names": ["PBD3B", "infantile Refsum disease", "Peroxisome Biogenesis Disorder 3B", "PEROXISOME BIOGENESIS DISORDER 3B", "peroxisome biogenesis disorder 3B", "peroxisome biogenesis disorder type 3B", "infantile phytanic acid storage disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder type 3B", "shortest_name_length": 5}
{"curie": "MONDO:0009482", "names": ["HH3", "KAL3", "Kallmann syndrome 3", "PROKR2 hypogonadotropic hypogonadism", "HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA", "hypogonadotropic hypogonadism 3 with or without anosmia", "hypogonadotropic hypogonadism caused by mutation in PROKR2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadotropic hypogonadism 3 with or without anosmia", "shortest_name_length": 3}
{"curie": "MONDO:0020759", "names": ["ECA1", "epilepsy, childhood absence, 1", "epilepsy, childhood absence, susceptibility to, 1", "EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, childhood absence, susceptibility to, 1", "shortest_name_length": 4}
{"curie": "MONDO:0020603", "names": ["CPXD", "CDPXD", "CDPX2", "Conradi", "Happle syndrome", "HAPPLE SYNDROME", "Conradi disease", "Happle Syndrome", "Conradi's syndrome", "Conradi-Hunermann Syndrome", "Conradi Hünermann Syndrome", "Conradi-Hünermann syndrome", "Hunermann Conradi Syndrome", "conradi hunermann syndrome", "CONRADI-HUNERMANN SYNDROME", "Hunermann-Conradi Syndrome", "Conradi-Hünermann Syndrome", "Conradi-Hunermann syndrome", "Conradi Hunermann syndrome", "Conradi Hunermann Syndrome", "conradi-hunermann syndrome", "Conradi-Hünermann Syndromes", "Conradi-Huenermann syndrome", "EBP chondrodysplasia punctata", "Conrad Hunermann Happle syndrome", "Conradi Hünermann Happle syndrome", "Conradi-Hunermann-Happle Syndrome", "Conradi Hunermann Happle Syndrome", "CONRADI-HUNERMANN-HAPPLE SYNDROME", "Conradi-Hünermann-Happle syndrome", "Conradi-Hunermann-Happle syndrome", "Conradi-Hünermann-Happle Syndrome", "Conradi Hünermann Happle Syndrome", "Conradi-Hünermann-Happle Syndromes", "Conradi-Hunermann-Happle Syndromes", "X Linked Chondrodysplasia Punctata 2", "X-linked chondrodysplasia punctata 2", "X-Linked Chondrodysplasia Punctata 2", "Chondrodysplasia Punctata 2, X Linked", "Chondrodysplasia Punctata 2, X-Linked", "Chondrodysplasia calcificans congenita", "Chondrodystrophia calcificans congenita", "X-linked chondrodysplasia punctata type 2", "X-Linked Dominant Chondrodysplasia Punctata", "X Linked Dominant Chondrodysplasia Punctata", "X-linked dominant chondrodysplasia punctata", "chondrodysplasia punctata 2 X-linked dominant", "Chondrodysplasia Punctata 2, X-Linked Dominant", "Chondrodysplasia Punctata 2, X Linked Dominant", "CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT", "chondrodysplasia punctata 2, X-linked dominant", "Chondrodysplasia punctata, Conradi-Hünermann type", "Chondrodysplasia punctata, X-linked dominant type", "Chondrodysplasia punctata, Conradi-Hunermann type", "chondrodysplasia punctata caused by mutation in EBP", "Chondrodysplasia punctata, X-linked dominant type (disorder)", "Chondrodysplasia punctata, Conradi-Hünermann type (disorder)", "chondrodysplasia punctata, X-linked dominant, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked chondrodysplasia punctata 2", "shortest_name_length": 4}
{"curie": "UMLS:C0334402", "names": ["cell granulosa theca tumor", "cell granulosa theca tumors", "granulosa cell-theca cell tumor", "Granulosa cell-theca cell tumor", "Theca cell-granulosa cell tumor", "Granulosa Cell-Theca Cell Tumor", "tumor; theca cell-granulosa cell", "tumor; granulosa cell-theca cell", "granulosa cell-theca cell; tumor", "Granulosa cell-theca cell tumour", "theca cell-granulosa cell; tumor", "Theca cell-granulosa cell tumour", "Theca cell - granulosa cell tumor", "Granulosa cell - theca cell tumor", "Theca cell - granulosa cell tumour", "Granulosa cell - theca cell tumour", "Granulosa cell-theca cell tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Granulosa cell-theca cell tumor", "shortest_name_length": 26}
{"curie": "MONDO:0012163", "names": ["IMD104", "IL7R Deficiency", "IMMUNODEFICIENCY 104", "immunodeficiency 104", "autosomal recessive T cell-negative, B-cell positive, NK cell-positive SCID", "autosomal recessive T cell-negative, B-cell negative, NK cell-positive SCID", "SCID, Autosomal Recessive, T Cell Negative, B Cell Positive, NK Cell Positive", "SCID, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive", "SCID, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-POSITIVE", "severe combined immunodeficiency, T cell-negative, B-cell/natural killer-cell positive", "severe combined immunodeficiency, T-cell negative, B-cell/natural killer cell-positive type", "severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive", "severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive", "SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-POSITIVE", "Severe Combined Immunodeficiency, Autosomal Recessive, T-Cell Negative, B Cell-Positive, NK Cell-Positive", "Severe Combined Immunodeficiency, Autosomal Recessive, T Cell Negative, B Cell Positive, NK Cell Positive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 104", "shortest_name_length": 6}
{"curie": "MONDO:0003509", "names": ["Pineal Choriocarcinoma", "pineal choriocarcinoma", "pineal area choriocarcinoma", "Pineal Area Choriocarcinoma", "pineal region choriocarcinoma", "Pineal Region Choriocarcinoma", "choriocarcinoma of pineal area", "Choriocarcinoma of Pineal Area", "Choriocarcinoma of Pineal Region", "choriocarcinoma of pineal region", "Choriocarcinoma of the Pineal Area", "choriocarcinoma of the pineal area", "choriocarcinoma of the pineal region", "Choriocarcinoma of the Pineal Region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pineal region choriocarcinoma", "shortest_name_length": 22}
{"curie": "UMLS:C0426552", "names": ["Interaretynoid leucoplakia", "Interaretynoid leukoplakia", "Interarytenoid leucoplakia", "Interarytenoid Leukoplakia", "Interarytenoid leukoplakia", "Interarytenoid leukoplakia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Interarytenoid leukoplakia", "shortest_name_length": 26}
{"curie": "UMLS:C0393786", "names": ["Idiopathic trigeminal neuralgia", "idiopathic trigeminal neuralgia", "Idiopathic Trigeminal Neuralgia", "Trigeminal Neuralgia, Idiopathic", "Neuralgia, Idiopathic Trigeminal", "Idiopathic Trigeminal Neuralgias", "Idiopathic trigeminal neuralgia (disorder)", "idiopathic trigeminal neuralgia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Trigeminal Neuralgia, Idiopathic", "shortest_name_length": 31}
{"curie": "MONDO:0032855", "names": ["NEDDFSA", "NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL SKELETAL ANOMALIES", "neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies", "shortest_name_length": 7}
{"curie": "UMLS:C3272612", "names": ["Colorectal L-Cell Glucagon-Like Peptide-Producing NET", "Colorectal L-Cell Glucagon-Like Peptide-Producing Neuroendocrine Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal L-Cell Glucagon-Like Peptide-Producing Neuroendocrine Tumor", "shortest_name_length": 53}
{"curie": "UMLS:C0151614", "names": ["Depletion;electrolyte", "ELECTROLYTE DEPLETION", "Electrolyte depletion", "electrolyte depletion", "depletion electrolytes", "Depletion of electrolyte", "ELECTROLYTE DEPLETION (NOS)", "Electrolyte depletion (NOS)", "Depletion of electrolyte (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Depletion of electrolyte", "shortest_name_length": 21}
{"curie": "MONDO:0010337", "names": ["MRXSBL", "OPHN1 XLMR", "OPHN1 syndrome", "MRX60, FORMERLY", "OPHN1 deficiency", "MRX60 (formerly)", "OPHN1- related XLID", "Oligophrenin-1 syndrome", "mental retardation, X-linked 60", "intellectual disability, X-linked 60", "MENTAL RETARDATION, X-LINKED 60, FORMERLY", "mental retardation, X-linked 60, formerly", "mental retardation X-linked 60 (formerly)", "OPHN1 XLMR, X-linked intellectual disability", "intellectual disability X-linked 60 (formerly)", "intellectual disability, X-linked 60, formerly", "X-linked intellectual Deficit with cerebellar Hypoplasia", "X-linked intellectual disability-cerebellar hypoplasia syndrome", "x-linked intellectual disability with cerebellar hypoplasia syndrome", "X-linked intellectual disability with cerebellar hypoplasia syndrome", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, BILLUART TYPE", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, BILLUART-TYPE", "X-linked intellectual disability with cerebellar hypoplasia syndrome (disorder)", "x-linked intellectual disability with cerebellar hypoplasia syndrome (diagnosis)", "mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance", "X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance", "MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE", "mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance", "Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance", "intellectual developmental disorder, X-linked syndromic, Billuart type, X-linked recessive", "intellectual disability X-linked with cerebellar hypoplasia and distinctive facial appearance", "intellectual disability, X-linked, with cerebellar hypoplasia and distinctive facial appearance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability-cerebellar hypoplasia syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0013612", "names": ["GPHYSD2", "GELEOPHYSIC dysplasia 2", "Geleophysic dysplasia 2", "geleophysic dysplasia 2", "GELEOPHYSIC DYSPLASIA 2", "FBN1 geleophysic dysplasia", "Geleophysic dysplasia type 2", "geleophysic dysplasia caused by mutation in FBN1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "geleophysic dysplasia 2", "shortest_name_length": 7}
{"curie": "UMLS:C5204256", "names": ["Renal Angiosarcoma", "Kidney Angiosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kidney Angiosarcoma", "shortest_name_length": 18}
{"curie": "MONDO:0010572", "names": ["OHS", "EDS9", "EDS IX", "EDS9, FORMERLY", "EDS9, formerly", "EDS IX, FORMERLY", "EDS IX, formerly", "EDS IX (formerly)", "Cutis laxa X-linked", "cutis laxa x-linked", "X-linked cutis laxa", "cutis laxa X-linked", "Cutis laxa, x-linked", "Cutis laxa, X-linked", "cutis laxa, X-linked", "Cutis Laxa, X-Linked", "occipital horn syndrome", "OCCIPITAL HORN SYNDROME", "Occipital horn syndrome", "Ehlers-Danlos syndrome type 9", "Ehlers-Danlos syndrome, type 9", "CUTIS LAXA, X-LINKED, FORMERLY", "Ehlers-Danlos syndrome type IX", "cutis laxa, X-linked, formerly", "Cutis laxa, x-linked (disorder)", "Cutis laxa, x-linked (diagnosis)", "Ehlers-Danlos syndrome type 9 X-linked", "occipital horn syndrome, X-linked recessive", "Ehlers-Danlos syndrome, occipital horn type", "Ehlers-Danlos syndrome, x-linked skeletal type", "Ehlers-Danlos syndrome, mental retardation type", "Ehlers-Danlos syndrome, occipital horn type, formerly", "EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY", "Ehlers-Danlos syndrome, occipital horn type (formerly)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "occipital horn syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0010651", "names": ["Mk", "MD", "MK", "MNK", "Menkes", "menke disease", "Menkes Disease", "menke syndrome", "Menkes disease", "MENKES DISEASE", "menkes disease", "Menkes syndrome", "Menkes' Disease", "MENKES SYNDROME", "Menkes Syndrome", "Menkea syndrome", "menkes syndrome", "Menkea Syndrome", "menkes' disease", "Syndrome, Menkea", "Menkea Syndromes", "Menkes' syndrome", "Menkes' Diseases", "menkes' syndrome", "Syndromes, Menkea", "Diseases, Menkes'", "Kinky hair disease", "Kinky Hair Disease", "kinky hair disease", "KINKY HAIR DISEASE", "Kinky Hair Syndrome", "kinky hair syndrome", "steely hair disease", "Kinky hair syndrome", "Kinky Hair Diseases", "Steely Hair Disease", "STEELY HAIR DISEASE", "Steely hair disease", "kinky; hair syndrome", "hair syndrome; kinky", "syndrome; kinky hair", "Trichopoliodystrophy", "Steely-hair syndrome", "Steely hair syndrome", "Diseases, Kinky Hair", "Hair Diseases, Kinky", "trichopoliodystrophy", "Steely Hair Diseases", "Steely Hair Syndrome", "steely hair syndrome", "Disease, Steely Hair", "MK - Menkes syndrome", "Syndrome, Steely Hair", "MNK - Menkes syndrome", "syndrome; steely hair", "Diseases, Steely Hair", "steely hair; syndrome", "Hair Diseases, Steely", "Steely Hair Syndromes", "Syndromes, Steely Hair", "Congenital hypocupremia", "Congenital Hypocupremia", "COPPER TRANSPORT DISEASE", "Congenital Hypocupremias", "copper transport disease", "Hypocupremia, Congenital", "Congenital hypocupraemia", "Copper transport disease", "Copper Transport Disease", "Menkes kinky hair disease", "Disease, Copper Transport", "Copper Transport Diseases", "kinky hair syndrome (KHS)", "Hypocupremias, Congenital", "Transport Disease, Copper", "Menkes' kinky hair disease", "Menkes Kinky Hair Syndrome", "Transport Diseases, Copper", "Menkes Kinky-Hair Syndrome", "Diseases, Copper Transport", "Menkes kinky hair syndrome", "X-Linked Copper Deficiency", "X-linked copper deficiency", "menkes kinky hair syndrome", "Menkes kinky-hair syndrome", "X Linked Copper Deficiency", "Menkes' kinky hair syndrome", "Menke's kinky hair syndrome", "menkes' kinky hair syndrome", "Deficiency, X-Linked Copper", "Copper Deficiency, X-Linked", "X-Linked Copper Deficiencies", "Deficiencies, X-Linked Copper", "X-linked copper malabsorption", "Copper Deficiencies, X-Linked", "Menkes kinky hair syndrome (MKHS)", "congenital hypocupraemia syndrome", "menkes disease, X-linked recessive", "Menkes kinky-hair syndrome (disorder)", "Menkes' kinky hair disease (diagnosis)", "hair; kink, Menkes (kinky hair syndrome)", "kink; hair, Menkes (kinky hair syndrome)", "sex-linked neurodegenerative disease with monilethrix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Menkes disease", "shortest_name_length": 2}
{"curie": "UMLS:C4524676", "names": ["LBCL with IRF4 Rearrangement", "Large B-Cell Lymphoma with IRF4 Rearrangement", "Large B-cell lymphoma with IRF4 rearrangement", "Large B-cell lymphoma with interferon regulatory factor 4 rearrangement", "Large B-cell lymphoma with interferon regulatory factor 4 rearrangement (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Large B-cell lymphoma with IRF4 rearrangement", "shortest_name_length": 28}
{"curie": "UMLS:C4721787", "names": ["Hodgkin; nodular sclerosis, lymphocytic depletion", "Hodgkin; lymphocytic depletion, nodular sclerosis", "Hodgkin's disease, nodular sclerosis, syncytial variant", "Hodgkin disease, nodular sclerosis, lymphocyte depletion", "Hodgkin's disease, nodular sclerosis - syncytial variant", "disease; Hodgkin's, nodular sclerosis, syncytial variant", "Hodgkin disease, nodular sclerosis - lymphocytic depletion", "Hodgkin's Disease, Nodular Sclerosis, Lymphocyte Depletion", "Hodgkin's disease, nodular sclerosis, lymphocytic depletion", "Hodgkin's disease, nodular sclerosis - lymphocytic depletion", "disease; Hodgkin's, nodular sclerosis, lymphocytic depletion", "nodular sclerosis Hodgkin lymphoma with lymphocytic depletion", "Hodgkin lymphoma, nodular sclerosis with lymphocytic depletion", "Hodgkin's disease, nodular sclerosis - lymphocytic depletion (disorder)", "nodular sclerosis Hodgkin lymphoma with lymphocytic depletion (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's Disease, Nodular Sclerosis, Lymphocyte Depletion", "shortest_name_length": 49}
{"curie": "UMLS:C1827377", "names": ["Slow acetylator", "Slow acetylator due to N-acetyltransferase enzyme variant", "Slow acetylator due to N-acetyltransferase enzyme variant (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Slow acetylator due to N-acetyltransferase enzyme variant", "shortest_name_length": 15}
{"curie": "MONDO:0017794", "names": ["Dup(X)(q12-q13.3)", "dup(X)(q12-q13.3)", "Xq12-q13.3 duplication syndrome", "Xq12-q13.3 duplication syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Xq12-q13.3 duplication syndrome", "shortest_name_length": 17}
{"curie": "MONDO:0003891", "names": ["bladder signet ring cell adenocarcinoma", "Bladder Signet Ring Cell Adenocarcinoma", "Bladder Signet-Ring Cell Adenocarcinoma", "Signet Ring Cell Adenocarcinoma of Bladder", "signet Ring cell adenocarcinoma of bladder", "urinary bladder Signet Ring adenocarcinoma", "Urinary Bladder Signet Ring Adenocarcinoma", "urinary bladder signet Ring adenocarcinoma", "urinary bladder signet ring cell carcinoma", "signet ring cell adenocarcinoma of bladder", "signet Ring cell adenocarcinoma of the bladder", "Signet Ring Cell Adenocarcinoma of the Bladder", "Signet Ring Cell Adenocarcinoma of Urinary Bladder", "signet Ring cell adenocarcinoma of urinary bladder", "Signet Ring Cell Adenocarcinoma of the Urinary Bladder", "signet Ring cell adenocarcinoma of the urinary bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder signet ring cell adenocarcinoma", "shortest_name_length": 39}
{"curie": "UMLS:C0014476", "names": ["EPERYTHROZOONOSIS", "eperythrozoonosis", "Eperythrozoonosis", "Eperythrozoonoses", "Eperythrozoonosis, NOS", "Eperythrozoonosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eperythrozoonosis", "shortest_name_length": 17}
{"curie": "UMLS:C2349020", "names": ["Unfavorable Non-Hodgkin Lymphoma", "Unfavorable Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unfavorable Non-Hodgkin Lymphoma", "shortest_name_length": 32}
{"curie": "MONDO:0022907", "names": ["cutaneous sclerosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous sclerosis", "shortest_name_length": 19}
{"curie": "MONDO:0011990", "names": ["BFNS3", "BFNC3", "Epilepsy, Benign Neonatal, 3", "seizures, benign familial neonatal, 3", "SEIZURES, BENIGN FAMILIAL NEONATAL, 3", "convulsions, benign familial neonatal, 3", "Convulsions, Benign Familial Neonatal, 3", "CONVULSIONS, BENIGN FAMILIAL NEONATAL, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "seizures, benign familial neonatal, 3", "shortest_name_length": 5}
{"curie": "UMLS:C2987397", "names": ["Gastric Medullary Carcinoma", "Gastric Carcinoma with Lymphoid Stroma", "Gastric Lymphoepithelioma-Like Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Carcinoma with Lymphoid Stroma", "shortest_name_length": 27}
{"curie": "MONDO:0007334", "names": ["PPS", "popliteal web syndrome", "popliteal pterygium syndrome", "faciogenitopopliteal syndrome", "popliteal pterygium syndrome 1", "facio-genito-popliteal syndrome", "autosomal dominant popliteal pterygium syndrome", "popliteal pterygium syndrome, autosomal dominant", "cleft lip/palate paramedian mucous cysts of the lower lip popliteal pterygium digital and genital anomalies", "cleft Lip/palate, paramedian mucous cysts of the Lower Lip, popliteal pterygium, digital and genital anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant popliteal pterygium syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C5557393", "names": ["Recurrent Distal Bile Duct Adenocarcinoma", "Recurrent Extrahepatic Cholangiocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Distal Bile Duct Adenocarcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0002760", "names": ["BLSC", "squamous cell bladder cancer", "bladder squamous cell cancer", "bladder epidermoid carcinoma", "Bladder Squamous Cell Cancer", "Bladder Epidermoid Carcinoma", "BLADDER CANCER SQUAMOUS CELL", "bladder cancer cell squamous", "Epidermoid Carcinoma of Bladder", "Bladder Squamous Cell Carcinoma", "bladder carcinoma cell squamous", "bladder squamous cell carcinoma", "Bladder squamous cell carcinoma", "epidermoid carcinoma of bladder", "bladder carcinomas cell squamous", "carcinoma, squamous cell, bladder", "Squamous Cell Carcinoma of Bladder", "squamous cell carcinoma of bladder", "Squamous cell carcinoma of bladder", "Epidermoid Carcinoma of the Bladder", "epidermoid carcinoma of the bladder", "Urinary Bladder Epidermoid Carcinoma", "urinary bladder epidermoid carcinoma", "Squamous Cell Carcinoma of the Bladder", "squamous cell carcinoma of the bladder", "epidermoid carcinoma of urinary bladder", "urinary bladder squamous cell carcinoma", "Epidermoid Carcinoma of Urinary Bladder", "Urinary Bladder Squamous Cell Carcinoma", "bladder cancer, squamous cell carcinoma", "Squamous Cell Carcinoma of Urinary Bladder", "squamous cell carcinoma of urinary bladder", "epidermoid carcinoma of the urinary bladder", "Epidermoid carcinoma of the urinary bladder", "Epidermoid Carcinoma of the Urinary Bladder", "Squamous cell carcinoma of bladder (disorder)", "squamous cell carcinoma of bladder (diagnosis)", "Squamous Cell Carcinoma of the Urinary Bladder", "squamous cell carcinoma of the urinary bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder squamous cell carcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0003304", "names": ["Tumor Royale", "Pachydermatocele", "pachydermatocele", "Pachydermatoceles", "Plexiform neuroma", "Plexiform Neuroma", "Plexiform Neuromas", "plexiform neuromas", "Neuroma, Plexiform", "Neuromas, Plexiform", "Plexiform neurofibroma", "Plexiform Neurofibroma", "plexiform neurofibroma", "neurofibroma plexiform", "Plexiform Neurofibromas", "Neurofibroma, Plexiform", "Plexiform neurofibromas", "Neurofibromas, Plexiform", "Elephantiasis Neuromatoses", "Elephantiasis Neuromatosis", "plexiform neurofibroma (disease)", "Plexiform neurofibroma (disorder)", "Plexiform neurofibroma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "plexiform neurofibroma", "shortest_name_length": 12}
{"curie": "MONDO:0006307", "names": ["Mixed GH-PRL Cell Adenoma", "mixed GH-PRL cell adenoma", "Mixed Somatolactotrope Adenoma", "mixed Somatolactotrope adenoma", "mixed somatotroph-lactotroph adenoma", "Mixed Somatotroph-Lactotroph Adenoma", "Mixed Somatotroph and Lactotroph Adenoma", "Mixed somatotroph and lactotroph adenoma", "Mixed Somatotroph and Lactotroph PitNET/Adenoma", "Mixed Somatotroph-Lactotroph Pituitary Gland Adenoma", "mixed somatotroph-lactotroph pituitary gland adenoma", "Mixed Somatotroph and Lactotroph Pituitary Neuroendocrine Tumor", "Mixed Somatotroph and Lactotroph Pituitary Neuroendocrine Tumor/Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed somatotroph-lactotroph pituitary gland adenoma", "shortest_name_length": 25}
{"curie": "MONDO:0033838", "names": ["radiation-induced plexopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radiation-induced plexopathy", "shortest_name_length": 28}
{"curie": "MONDO:0030525", "names": ["EBS2B", "EPIDERMOLYSIS BULLOSA SIMPLEX 2B, KOEBNER TYPE", "epidermolysis bullosa simplex 2B, generalized intermediate", "EPIDERMOLYSIS BULLOSA SIMPLEX 2B, GENERALIZED INTERMEDIATE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolysis bullosa simplex 2B, generalized intermediate", "shortest_name_length": 5}
{"curie": "UMLS:C1709579", "names": ["Pleural Synovial Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pleural Synovial Sarcoma", "shortest_name_length": 24}
{"curie": "MONDO:0006960", "names": ["Sciatic Neuropathy", "Sciatic neuropathy", "sciatic neuropathy", "Neuropathy, Sciatic", "NEUROPATHY, SCIATIC", "Sciatic Neuropathies", "Neuropathies, Sciatic", "Sciatic Nerve Disease", "Nerve Disease, Sciatic", "Sciatic Nerve Diseases", "Nerve Diseases, Sciatic", "Sciatic nerve--Diseases", "Sciatic nerve neuropathy", "neuropathy; sciatic nerve", "n.ischiadicus; neuropathic", "Sciatic neuropathy (disorder)", "sciatic neuropathy (diagnosis)", "disease (or disorder); nerve, sciatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sciatic neuropathy", "shortest_name_length": 18}
{"curie": "UMLS:C4763506", "names": ["Composite Paraganglioma", "Composite paraganglioma", "Composite Pheochromocytoma and Paraganglioma", "Composite paraganglioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Composite paraganglioma", "shortest_name_length": 23}
{"curie": "UMLS:C3267051", "names": ["Chronic graft versus host disease in liver"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic graft versus host disease in liver", "shortest_name_length": 42}
{"curie": "MONDO:0017909", "names": ["GSSD", "5-Oxoprolinuria", "5 oxoprolinuria", "5-OXOPROLINURIA", "5-oxoprolinuria", "5-oxoprolinemia", "Pyroglutamicaciduria", "pyroglutamicaciduria", "Pyroglutamic Acidemia", "Pyroglutamic Aciduria", "PYROGLUTAMIC ACIDURIA", "pyroglutamic acidemia", "pyroglutamic aciduria", "Pyroglutamic aciduria", "Pyroglutamic acidemia", "Pyroglutamic acidaemia", "oxoprolinase deficiency", "glutathione synthetase deficiency", "GLUTATHIONE SYNTHETASE DEFICIENCY", "Glutathione synthetase deficiency", "Glutathione Synthetase Deficiency", "Deficiency of glutathione synthase", "Gluthathione synthetase deficiency", "gluthathione synthetase deficiency", "Deficiency of Glutathione Synthase", "Deficiency of glutathione synthetase", "Deficiency of Glutathione Synthetase", "Reduced glutathione synthetase level", "inherited glutathione synthetase deficiency", "Glutathione synthetase deficiency (disorder)", "inborn glutathione synthase activity disorder", "Deficiency of glutathione synthase (disorder)", "inborn error of glutathione synthase activity", "gluthathione synthetase deficiency (diagnosis)", "rare inborn error of glutathione synthase activity", "Glutathione synthase deficiency with 5-oxoprolinuria", "Glutathione synthetase deficiency with 5-oxoprolinuria", "Glutathione synthase deficiency with 5-oxoprolinuria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited glutathione synthetase deficiency", "shortest_name_length": 4}
{"curie": "UMLS:C2937217", "names": ["nasal sinus cyst", "Nasal sinus cyst", "Nasal Sinus Cyst", "Cyst of nasal sinus", "Cyst of Nasal Sinus", "Paranasal Sinus Cyst", "Paranasal sinus cyst", "Cyst of the Nasal Sinus", "Mucocele of nasal sinus", "Mucous cyst of nasal sinus", "nasal sinus cyst (diagnosis)", "Cyst of nasal sinus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cyst of nasal sinus", "shortest_name_length": 16}
{"curie": "MONDO:0003204", "names": ["Villous Adenocarcinoma", "Villous adenocarcinoma", "villous adenocarcinoma", "villous adenocarcinoma (diagnosis)", "Villous adenocarcinoma (morphologic abnormality)", "villous adenocarcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "villous adenocarcinoma", "shortest_name_length": 22}
{"curie": "UMLS:C3897743", "names": ["Recurrent Kidney Neoplasm", "Recurrent Childhood Renal Neoplasm", "Recurrent Childhood Kidney Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Kidney Neoplasm", "shortest_name_length": 25}
{"curie": "MONDO:0004125", "names": ["rectal leiomyoma", "rectum leiomyoma", "Rectal Leiomyoma", "Leiomyoma of Rectum", "leiomyoma of rectum", "Leiomyoma of the Rectum", "leiomyoma of the rectum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rectum leiomyoma", "shortest_name_length": 16}
{"curie": "MONDO:0006190", "names": ["ELST", "Heffner tumor", "Heffner Tumor", "Heffner tumour", "Endolymphatic Sac Tumor", "endolymphatic sac tumor", "Endolymphatic sac tumor", "Endolymphatic sac tumour", "tumor of endolymphatic sac", "endolymphatic sac neoplasm", "neoplasm of endolymphatic sac", "Neoplasm of endolymphatic sac", "endolymphatic sac tumor (disease)", "endolymphatic sac neoplasm (disease)", "Aggressive papillary middle ear tumor", "Aggressive papillary middle ear tumour", "Neoplasm of endolymphatic sac (disorder)", "aggressive papillary tumor of the temporal bone", "Low-grade adenocarcinoma of endolymphatic sac origin", "Low-Grade Papillary Adenocarcinoma of Endolymphatic Sac Origin", "Low Grade Papillary Adenocarcinoma of Endolymphatic Sac Origin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endolymphatic sac tumor", "shortest_name_length": 4}
{"curie": "MONDO:0016831", "names": ["linear hamartoma syndrome", "linear verrucous nevus syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "linear verrucous nevus syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0000409", "names": ["Amnionitis", "amnionitis", "membranitis", "Membranitis", "chorioamnionitis", "Chorioamnionitis", "CHORIOAMNIONITIS", "Chorioamnionitides", "intra-amniotic infection", "Chorioamnionitis (disorder)", "fetal membrane inflammation", "chorioamnionitis (diagnosis)", "inflammation of fetal membrane", "Chorioamnionitis, unspecified trimester, not applicable or unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chorioamnionitis", "shortest_name_length": 10}
{"curie": "MONDO:0035696", "names": ["Incomplete septal fibrosis", "incomplete septal cirrhosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "incomplete septal cirrhosis", "shortest_name_length": 26}
{"curie": "UMLS:C4743980", "names": ["Recurrent Extremity Melanoma", "Recurrent Melanoma of the Extremity", "Recurrent Cutaneous Melanoma of the Extremity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Cutaneous Melanoma of the Extremity", "shortest_name_length": 28}
{"curie": "MONDO:0054577", "names": ["BDPLT21", "bleeding disorder, platelet-type, 21", "BLEEDING DISORDER, PLATELET-TYPE, 21"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bleeding disorder, platelet-type, 21", "shortest_name_length": 7}
{"curie": "MONDO:0009472", "names": ["Slow acetylation", "acetylation, slow", "ACETYLATION, SLOW", "acetylation, Fast", "ACETYLATION, FAST", "Slow acetylator status", "INH inactivation, Fast", "INH INACTIVATION, SLOW", "INH inactivation, slow", "INH INACTIVATION, FAST", "slow acetylator phenotype", "Fast acetylator phenotype", "SLOW ACETYLATOR PHENOTYPE", "FAST ACETYLATOR PHENOTYPE", "Isoniazid inactivation, slow", "ISONIAZID INACTIVATION, SLOW"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acetylation, slow", "shortest_name_length": 16}
{"curie": "UMLS:C1334421", "names": ["Grade 1 Conjunctival Intraepithelial Neoplasia", "Grade I Conjunctival Intraepithelial Neoplasia", "Low Grade Conjunctival Intraepithelial Neoplasia", "Low Grade Conjunctival Squamous Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Grade Conjunctival Squamous Intraepithelial Neoplasia", "shortest_name_length": 46}
{"curie": "MONDO:0015168", "names": ["AMC", "myodysplasia", "Otto syndrome", "Rossi syndrome", "amyoplasia congenita", "Guerin-Stern syndrome", "congenital amyoplasia", "Guérin-Stern syndrome", "rocher-Sheldon syndrome", "Arthromyodysplasia congenita", "congenital arthromyodysplasia", "myodystrophia fetalis deformans", "multiple congenital arthrogryposis", "arthrogryposis multiplex congenita", "fibrous ankylosis of multiple joints"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis multiplex congenita", "shortest_name_length": 3}
{"curie": "UMLS:C4528639", "names": ["Stage I Low-CSD Melanoma AJCC v7", "Stage I Superficial Spreading Melanoma AJCC v7", "Stage I Superficial Spreading Cutaneous (Skin) Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Low-CSD Melanoma AJCC v7", "shortest_name_length": 32}
{"curie": "UMLS:C0522182", "names": ["Nosophobia", "nosophobia", "Pathophobia", "pathophobia", "disease fear", "fear illness", "Disease phobia", "Fear of disease", "fear of disease", "Phobia, disease", "fear of illness", "Fear (of);illness", "Fear (of);disease", "Nosophobia (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nosophobia", "shortest_name_length": 10}
{"curie": "UMLS:C0854866", "names": ["Recurrent Non-Hodgkin Lymphoma", "Non-Hodgkin's Lymphoma Relapsed", "Relapsed Non-Hodgkin's Lymphoma", "Recurrent Non-Hodgkin's Lymphoma", "Non-Hodgkin's lymphoma recurrent", "Non-Hodgkin's lymphoma NOS recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Non-Hodgkin Lymphoma", "shortest_name_length": 30}
{"curie": "MONDO:0017995", "names": ["spondylocostal dysostosis-hypospadias-intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondylocostal dysostosis-hypospadias-intellectual disability syndrome", "shortest_name_length": 70}
{"curie": "MONDO:0010901", "names": ["HEC syndrome", "HEC SYNDROME", "HYDROCEPHALUS, ENDOCARDIAL FIBROELASTOSIS, AND CATARACTS", "hydrocephalus, endocardial fibroelastosis, and cataracts", "Hydrocephalus, endocardial fibroelastosis, and cataracts", "hydrocephalus-endocardial fibroelastosis-cataract syndrome", "Hydrocephalus-endocardial fibroelastosis-cataract syndrome", "HEC (hydrocephalus, endocardial fibroelastosis, cataract) syndrome", "Hydrocephalus with endocardial fibroelastosis and cataract syndrome", "Hydrocephalus with endocardial fibroelastosis and cataract syndrome (disorder)", "communicating hydrocephalus, endocardial fibroelastosis (EFE) and congenital cataracts", "Communicating hydrocephalus, endocardial fibroelastosis (EFE) and congenital cataracts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HEC syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0019130", "names": ["tubular renal disease-cardiomyopathy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tubular renal disease-cardiomyopathy syndrome", "shortest_name_length": 45}
{"curie": "UMLS:C1334563", "names": ["Malignant Bladder Paraganglioma", "Metastatic Bladder Paraganglioma", "malignant paraganglioma of bladder", "Malignant Paraganglioma of Bladder", "Malignant Paraganglioma of the Bladder", "Malignant Urinary Bladder Paraganglioma", "Malignant Paraganglioma of Urinary Bladder", "malignant paraganglioma of bladder (diagnosis)", "Malignant Paraganglioma of the Urinary Bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Bladder Paraganglioma", "shortest_name_length": 31}
{"curie": "UMLS:C4683418", "names": ["Stage I Differentiated Thyroid Gland Cancer 55 Years and Older", "Stage I Differentiated Thyroid Gland Carcinoma 55 Years and Older AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Differentiated Thyroid Gland Carcinoma 55 Years and Older AJCC v8", "shortest_name_length": 62}
{"curie": "MONDO:0005872", "names": ["Neural Tumor", "neural tumor", "Neural Neoplasm", "neural neoplasm", "nervous system tumor", "Nervous System Tumor", "Nervous system cancer", "nervous system tumors", "cancer nervous system", "nervous system cancer", "Nervous System Tumour", "Tumor, Nervous System", "nervous system tumour", "Nervous System Tumors", "Tumors, Nervous System", "cancers nervous system", "Nervous system--Tumors", "Nervous system--Cancer", "nervous system tumours", "Nervous System Neoplasm", "Tumor of nervous system", "Nervous system neoplasm", "Tumor of Nervous System", "nervous system neoplasm", "Nervous System Neoplasms", "Neoplasm, Nervous System", "cancer of nervous system", "Tumour of nervous system", "Neoplasms, Nervous System", "Neoplasm of nervous system", "Neoplasm of Nervous System", "neoplasm of nervous system", "Tumor of the Nervous System", "Tumor of the nervous system", "tumor of the nervous system", "Nervous system neoplasm NOS", "tumors of the nervous system", "Tumors of the Nervous System", "Tumour of the nervous system", "Neoplasm of the Nervous System", "malignant neurologic neoplasms", "Malignant Nervous System Tumor", "malignant nervous system tumor", "Malignant neurologic neoplasms", "Neoplasm of the nervous system", "Neoplasia of the nervous system", "Malignant neoplasm nervous system", "malignant nervous system neoplasm", "Malignant nervous system neoplasm", "Malignant tumor of nervous system", "malignant tumor of nervous system", "Malignant Tumor of Nervous System", "Malignant Nervous System Neoplasm", "Malignant tumour of nervous system", "Nervous System Neoplasms, Malignant", "nervous system neoplasms, malignant", "malignant neoplasm of nervous system", "Malignant Neoplasm of Nervous System", "Malignant neoplasm of nervous system", "Neoplasm of nervous system (disorder)", "malignant tumor of the nervous system", "Malignant nervous system neoplasm NOS", "Malignant Tumor of the Nervous System", "malignant neoplasm of the nervous system", "Malignant Neoplasm of the Nervous System", "Malignant neoplasm of nervous system NOS", "Malignant neoplasm of nervous system (disorder)", "malignant neoplasm of nervous system (diagnosis)", "Malignant neoplasm of nervous system, part unspecified", "Neuroepithelial, Perineurial, and Schwann Cell Neoplasm", "Malignant neoplasm of other and unspecified parts of nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nervous system cancer", "shortest_name_length": 12}
{"curie": "MONDO:0007352", "names": ["PAPRS", "Papillorenal syndrome", "PAPILLORENAL syndrome", "PAPILLORENAL SYNDROME", "Papillorenal Syndrome", "papillorenal syndrome", "Papillo-renal syndrome", "renal coloboma syndrome", "RENAL-COLOBOMA SYNDROME", "Renal-coloboma syndrome", "renal-coloboma syndrome", "Renal Coloboma Syndrome", "Renal coloboma syndrome", "Coloboma-Ureteral-Renal Syndrome", "Renal coloboma syndrome (disorder)", "Optic Nerve Coloboma Renal Syndrome", "Optic nerve coloboma with renal disease", "optic nerve coloboma with renal disease", "OPTIC NERVE COLOBOMA WITH RENAL DISEASE", "CAKUT WITH OR WITHOUT OCULAR ABNORMALITIES", "COLOBOMA OF OPTIC NERVE WITH RENAL DISEASE", "Coloboma of optic nerve with renal disease", "CAKUT with or without ocular abnormalities", "coloboma of optic nerve with renal disease", "Renal-Coloboma Syndrome With Macular Abnormalities", "RENAL-COLOBOMA SYNDROME WITH MACULAR ABNORMALITIES", "renal-coloboma syndrome with macular abnormalities", "optic coloboma, vesicoureteral reflux and renal anomalies", "OPTIC COLOBOMA, VESICOURETERAL REFLUX, AND RENAL ANOMALIES", "Optic coloboma, vesicoureteral reflux, and renal anomalies", "optic coloboma, vesicoureteral reflux, and renal anomalies", "papillo-renal syndrome, optic nerve coloboma with renal disease", "congenital anomalies of the kidney and urinary tract with or without ocular abnormalities", "CONGENITAL ANOMALIES OF THE KIDNEY AND URINARY TRACT WITH OR WITHOUT OCULAR ABNORMALITIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal coloboma syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0007018", "names": ["Vulvitis", "vulvitis", "VULVITIS", "Vulvitides", "Vulvitis NOS", "Vulvitis, NOS", "Vulvitis (disorder)", "vulvitis (diagnosis)", "vulvitis was observed", "vulvitis (physical finding)", "mammalian vulva inflammation", "inflammation of mammalian vulva"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvitis", "shortest_name_length": 8}
{"curie": "MONDO:0060549", "names": ["CAKUTHED", "congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay", "CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay", "shortest_name_length": 8}
{"curie": "UMLS:C0851353", "names": ["Hemic and Lymphatic Diseases", "Blood and Lymphatic Disorders", "blood and lymphatic system disorders", "Blood and Lymphatic System Disorders", "Blood and lymphatic system disorders", "Hematopoietic and Lymphoid System Disease", "Hematopoietic and Lymphoid System Disorder", "blood and lymphatic system disorders (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Blood and lymphatic system disorders", "shortest_name_length": 28}
{"curie": "UMLS:C5421307", "names": ["Refractory Thyroid Gland Anaplastic Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Thyroid Gland Anaplastic Carcinoma", "shortest_name_length": 45}
{"curie": "UMLS:C0853811", "names": ["Croup infectious"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Croup infectious", "shortest_name_length": 16}
{"curie": "MONDO:0017307", "names": ["tyrosine; metabolic disorder", "metabolic disorder; tyrosine", "Disorder of tyrosine metabolism", "disorder of tyrosine metabolism", "tyrosine metabolism disturbances", "Disorders of tyrosine metabolism", "Disturbance of tyrosine metabolism", "Disturbance of tyrosine metabolism, NOS", "Disorder of tyrosine metabolism (disorder)", "tyrosine metabolism disturbances (diagnosis)", "Disorder of tyrosine metabolism, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of tyrosine metabolism", "shortest_name_length": 28}
{"curie": "UMLS:C0866108", "names": ["Nephrotic syndrome with lesion of focal glomerulosclerosis", "Nephrotic Syndrome with Lesion of Focal Glomerulosclerosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome with Lesion of Focal Glomerulosclerosis", "shortest_name_length": 58}
{"curie": "MONDO:0007384", "names": ["CORNEAL HYPESTHESIA, FAMILIAL", "corneal hypesthesia, familial", "Corneal hypesthesia, familial", "familial trigeminal anesthesia", "trigeminal anesthesia, familial", "TRIGEMINAL ANESTHESIA, FAMILIAL", "Trigeminal anesthesia, familial", "Congenital trigeminal anesthesia", "congenital trigeminal anesthesia", "Congenital trigeminal anaesthesia", "Congenital trigeminal anesthesia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital trigeminal anesthesia", "shortest_name_length": 29}
{"curie": "MONDO:0005969", "names": ["SLE", "ENCEPHALITIS C", "st louis encephalitis", "St Louis encephalitis", "encephalitis; St Louis", "St. Louis Encephalitis", "St. Louis encephalitis", "Encephalitis, St-Louis", "st. Louis encephalitis", "st. louis encephalitis", "St Louis; encephalitis", "St. Louis viral disease", "Encephalitis, St. Louis", "saint louis encephalitis", "Saint Louis encephalitis", "Saint Louis Encephalitis", "ENCEPHALITIS, SAINT LOUIS", "Encephalitis, Saint Louis", "viral encephalitis St. Louis", "St. Louis encephalitis (SLE)", "St. Louis Viral Encephalitis", "Type C Lethargic Encephalitis", "Type C lethargic encephalitis", "Encephalitis, Viral, St. Louis", "SLE - Saint Louis encephalitis", "Lethargic Encephalitis, Type C", "St. Louis encephalitis (diagnosis)", "St. Louis encephalitis virus infection", "Saint Louis encephalitis virus infection", "St. Louis encephalitis virus neuroinvasive disease", "Saint Louis encephalitis virus infection (disorder)", "Neuroinvasive St. Louis encephalitis virus infection", "St. Louis encephalitis virus infectious encephalitis", "Neuroinvasive Saint Louis encephalitis virus infection", "St. Louis encephalitis virus caused infectious encephalitis", "Neuroinvasive Saint Louis encephalitis virus infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "st. Louis encephalitis", "shortest_name_length": 3}
{"curie": "UMLS:C0279549", "names": ["Ph- CML", "Ph Negative CML", "Ph1 negative CML", "Ph- Chronic Myelogenous Leukemia", "Philadelphia Chromosome Negative CML", "CML, Philadelphia chromosome negative", "CGL, Philadelphia chromosome negative", "Ph Negative Chronic Myelogenous Leukemia", "Ph' negative chronic myelogenous leukemia", "Ph1 negative chronic myelogenous leukemia", "Ph' Negative Chronic Granulocytic Leukemia", "Ph' Chromosome Negative Chronic Myeloid Leukemia", "Ph1 Chromosome Negative Chronic Myelocytic Leukemia", "Ph' Chromosome Negative Chronic Myelocytic Leukemia", "Ph1 Chromosome Negative Chronic Myelogenous Leukemia", "Ph' Chromosome Negative Chronic Granulocytic Leukemia", "Philadelphia Chromosome Negative Chronic Myeloid Leukemia", "Philadelphia Chromosome Negative Chronic Myelocytic Leukemia", "chronic myelocytic leukemia, Philadelphia chromosome negative", "Philadelphia chromosome negative chronic myelogenous leukemia", "Philadelphia Chromosome Negative Chronic Myelogenous Leukemia", "Philadelphia Chromosome Negative Chronic Granulocytic Leukemia", "chronic myelogenous leukemia, Philadelphia chromosome negative", "myelocytic leukemia, chronic, Philadelphia chromosome negative", "Philadelphia chromosome negative chronic myelogenous leukaemia", "chronic granulocytic leukemia, Philadelphia chromosome negative", "myelogenous leukemia, chronic, Philadelphia chromosome negative", "granulocytic leukemia, chronic, Philadelphia chromosome negative", "Philadelphia chromosome negative chronic myelogenous leukemia (disorder)", "Philadelphia chromosome negative chronic myelogenous leukemia (diagnosis)", "Philadelphia Chromosome Negative BCR-ABL1 Positive Chronic Myelogenous Leukemia", "Philadelphia Chromosome Negative, BCR-ABL1 Positive Chronic Myelogenous Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Philadelphia chromosome negative chronic myelogenous leukemia", "shortest_name_length": 7}
{"curie": "UMLS:C1880169", "names": ["Connective and Soft Tissue Neoplasm (Antiquated)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Connective and Soft Tissue Neoplasm (Antiquated)", "shortest_name_length": 48}
{"curie": "MONDO:0005061", "names": ["LUAD", "Adenocarcinoma", "Lung Adenocarcinoma", "Lung adenocarcinoma", "ADENOCARCINOMA LUNG", "lung adenocarcinoma", "adenocarcinoma lung", "Adenocarcinoma lung", "LUNG, ADENOCARCINOMA", "Lung Adenocarcinomas", "adenocarcinomas lung", "adenocarcinoma lungs", "Adenocarcinoma, Lung", "Adenocarcinomas, Lung", "adenocarcinoma of lung", "of lung adenocarcinoma", "ADENOCARCINOMA OF LUNG", "Adenocarcinoma of Lung", "Adenocarcinoma of lung", "Lung adenocarcinoma NOS", "Pulmonary adenocarcinoma", "adenocarcinoma lung cancer", "Adenocarcinoma of the Lung", "LUNG CANCER ADENOCARCINOMA", "lung cancer adenocarcinoma", "adenocarcinoma cancer lung", "adenocarcinoma of the lung", "lung cancer, adenocarcinoma", "lung, adenocarcinoma of the", "adenocarcinoma cancer lungs", "LUNG CANCER, ADENOCARCINOMA", "Nonsmall Cell Adenocarcinoma", "nonsmall cell adenocarcinoma", "Non-Small Cell Adenocarcinoma", "bronchogenic lung adenocarcinoma", "Adenocarcinoma of lung (disorder)", "[OBSOLETE] Adenocarcinoma of lung", "adenocarcinoma of lung (diagnosis)", "non-small cell lung adenocarcinoma", "non-oat cell adenocarcinoma of the lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung adenocarcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0003674", "names": ["semi", "subendocardial heart attack", "subendocardial myocardial infarction", "Subendocardial myocardial infarction", "MYOCARDIAL INFARCTION SUBENDOCARDIAL", "subendocardial; myocardial infarction", "MYOCARDIAL INFARCTION (SUBENDOCARDIAL)", "infarction; myocardial, subendocardial", "subendocardial myocardial infarction (SEMI)", "Subendocardial myocardial infarction (disorder)", "Subendocardial Myocardial Infarction by EKG Finding", "Subendocardial Myocardial Infarction by ECG Finding", "subendocardium layer myocardial infarction (disease)", "myocardial infarction (disease) of subendocardium layer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subendocardial myocardial infarction", "shortest_name_length": 4}
{"curie": "MONDO:0010977", "names": ["BROD", "Brody Disease", "BRODY DISEASE", "Brody disease", "BRODY MYOPATHY", "Brody myopathy", "Brody myopathy (disorder)", "Autosomal recessive Brody myopathy", "sarcoplasmic reticulum -Ca2+ATPase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brody myopathy", "shortest_name_length": 4}
{"curie": "UMLS:C2741638", "names": ["ULCER STRESS", "Stress ulcer", "Ulcer stress", "stress ulcer", "STRESS ULCER", "Stress Ulcer", "STRESS ULCERS", "Curling Ulcer", "Ulcer, stress", "Stress ulcer, NOS", "Stress ulcer (disorder)", "stress induced peptic ulcer", "stress induced peptic ulcer (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stress ulcer", "shortest_name_length": 12}
{"curie": "UMLS:C0586367", "names": ["Mild Colon Dysplasia", "Mild Colonic Dysplasia", "Mild dysplasia of colon", "Mild Dysplasia of Colon", "Low-Grade Colon Dysplasia", "Low Grade Colon Dysplasia", "Colon dysplasia low grade", "Low Grade Colonic Dysplasia", "Mild Dysplasia of the Colon", "Low-Grade Colonic Dysplasia", "Low Grade Dysplasia of Colon", "Low-Grade Dysplasia of Colon", "Low Grade Dysplasia of the Colon", "Low-Grade Dysplasia of the Colon", "Mild dysplasia of colon (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mild dysplasia of colon", "shortest_name_length": 20}
{"curie": "MONDO:0006224", "names": ["Gastric Hamartoma", "Hamartoma of stomach", "hamartoma of stomach", "Hamartoma of Stomach", "hamartoma of the stomach", "Hamartoma of the Stomach", "Gastric Hamartomatous Polyp", "stomach hamartoma (disease)", "gastric hamartomatous polyp", "Hamartoma of stomach (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric hamartomatous polyp", "shortest_name_length": 17}
{"curie": "MONDO:0012247", "names": ["SCA27", "congenital nystagmus 4", "spinocerebellar ataxia 27", "SPINOCEREBELLAR ATAXIA 27", "Spinocerebellar ataxia 27", "Spinocerebellar ataxia type 27", "spinocerebellar ataxia type 27", "SCA27 Spinocerebellar ataxia 27", "autosomal dominant congenital nystagmus 4", "Spinocerebellar ataxia type 27 (disorder)", "cerebellar ataxia autosomal dominant FGF14-related", "cerebellar ataxia, autosomal dominant, Fgf14-related", "Cerebellar ataxia, autosomal dominant, FGF14-related", "vestibulocerebellar disorder with predominant ocular signs"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia type 27", "shortest_name_length": 5}
{"curie": "UMLS:C3544185", "names": ["Occupational exposure to product"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Occupational exposure to product", "shortest_name_length": 32}
{"curie": "UMLS:C1336317", "names": ["Stage II Skin Cancer", "Skin Cancer Stage II", "Skin Carcinoma Stage II", "Carcinoma of Skin Stage II", "Stage II Skin Cancer AJCC v7", "Carcinoma of the Skin Stage II", "stage II nonmelanoma skin cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Skin Cancer", "shortest_name_length": 20}
{"curie": "MONDO:0060591", "names": ["IMDDHH", "immunodeficiency, developmental delay, and hypohomocysteinemia", "IMMUNODEFICIENCY, DEVELOPMENTAL DELAY, AND HYPOHOMOCYSTEINEMIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency, developmental delay, and hypohomocysteinemia", "shortest_name_length": 6}
{"curie": "MONDO:0001059", "names": ["lymphoma stomach", "Gastric Lymphoma", "LYMPHOMA GASTRIC", "stomach lymphoma", "gastric lymphoma", "GASTRIC LYMPHOMA", "lymphoma gastric", "Gastric lymphoma", "gastric lymphomas", "Lymphoma of Stomach", "Lymphoma of stomach", "lymphoma of stomach", "lymphoma of the stomach", "Lymphoma of the stomach", "Lymphoma of the Stomach", "primary gastric lymphoma", "Primary Gastric Lymphoma", "Primary gastric lymphoma", "Gastric lymphoma (disorder)", "malignant lymphoma of stomach", "Familial primary gastric lymphoma", "malignant lymphoma of stomach (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric lymphoma", "shortest_name_length": 16}
{"curie": "MONDO:0008595", "names": ["Trichoepitheliomas, Multiple Desmoplastic", "trichoepitheliomas, multiple desmoplastic", "TRICHOEPITHELIOMAS, MULTIPLE DESMOPLASTIC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichoepitheliomas, multiple desmoplastic", "shortest_name_length": 41}
{"curie": "UMLS:C3273019", "names": ["eHCC", "Early Hepatocellular Cancer", "Early Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Early Hepatocellular Carcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0010796", "names": ["Parkinson disease, mitochondrial", "Parkinson Disease, Mitochondrial", "PARKINSON DISEASE, MITOCHONDRIAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parkinson disease, mitochondrial", "shortest_name_length": 32}
{"curie": "UMLS:C0751362", "names": ["cataplexy narcolepsy", "narcolepsy cataplexy", "Narcolepsy and cataplexy", "Cataplexy and narcolepsy", "Narcolepsy with cataplexy", "narcolepsy with cataplexy", "Narcolepsy, with cataplexy", "Narcolepsy-Cataplexy Syndrome", "Narcolepsy Cataplexy Syndrome", "Syndrome, Narcolepsy-Cataplexy", "Narcolepsy-Cataplexy Syndromes", "Syndromes, Narcolepsy-Cataplexy", "Cataplexy and narcolepsy (disorder)", "narcolepsy with cataplexy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Narcolepsy-Cataplexy Syndrome", "shortest_name_length": 20}
{"curie": "MONDO:0003474", "names": ["Tanycytic ependymoma", "Tanycytic Ependymoma", "tanycytic ependymoma", "Ependymoma, tanycytic", "Ependymoma, tanycytic (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tanycytic ependymoma", "shortest_name_length": 20}
{"curie": "MONDO:0007705", "names": ["HEINZ BODY ANEMIA", "Heinz body anemia", "ANEMIA HEINZ BODY", "Anemia Heinz body", "Heinz body anemias", "HEINZ BODY ANEMIAS", "Anaemia Heinz body", "Heinz body anaemia", "Heinz Body Anemias", "anemia; Heinz body", "Heinz body; anemia", "Heinz body anemias, alpha-"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Heinz body anemia", "shortest_name_length": 17}
{"curie": "MONDO:0400003", "names": ["skeletal fluorosis", "fluorosis of the skeleton"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skeletal fluorosis", "shortest_name_length": 18}
{"curie": "MONDO:0007231", "names": ["brachytelephalangy-dysmorphism-Kallmann syndrome", "Brachytelephalangy characteristic facies Kallmann", "Characteristic craniofacial appearance and brachytelephalangy", "Brachytelephalangy with Characteristic Facies and Kallmann Syndrome", "BRACHYTELEPHALANGY with characteristic facies and Kallmann syndrome", "BRACHYTELEPHALANGY WITH CHARACTERISTIC FACIES AND KALLMANN SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachytelephalangy-dysmorphism-Kallmann syndrome", "shortest_name_length": 48}
{"curie": "MONDO:0003448", "names": ["spiradenoma", "Spiradenoma", "Spiradenomas", "Spiradenoma, NOS", "benign spiradenoma", "Spiradenoma eccrine", "eccrine spiradenoma", "Eccrine spiradenoma", "spiroma/spiradenoma", "Eccrine Spiradenoma", "Benign Eccrine Spiradenoma", "benign eccrine spiradenoma", "Eccrine spiradenoma of skin", "eccrine spiradenoma of skin", "Eccrine spiradenoma of skin (disorder)", "eccrine spiradenoma (morphologic abnormality)", "Eccrine spiradenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign spiradenoma", "shortest_name_length": 11}
{"curie": "UMLS:C4721645", "names": ["Stage II Esophagus Adenocarcinoma", "Stage II Esophageal Adenocarcinoma", "Esophageal Adenocarcinoma, Stage II", "Oesophageal Adenocarcinoma Stage II", "Stage II Adenocarcinoma of Esophagus", "Stage II Adenocarcinoma of the Esophagus", "Stage II Esophageal Adenocarcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Esophageal Adenocarcinoma AJCC v7", "shortest_name_length": 33}
{"curie": "UMLS:C1336487", "names": ["Stage I Supradiaphragmatic Hodgkin Lymphoma Lymphocyte Depleted", "Stage I Supradiaphragmatic Lymphocyte Depleted Hodgkin Lymphoma", "Stage I Supradiaphragmatic Lymphocyte Depleted Hodgkin's Lymphoma", "Stage I Supradiaphragmatic Hodgkin's Lymphoma Lymphocyte Depleted", "Stage I Hodgkin's Lymphoma Lymphocyte Depleted above the Diaphragm", "Stage I Supradiaphragmatic Hodgkin's Disease Lymphocyte Depletion Type", "Stage I Hodgkin's Disease Lymphocyte Depletion Type above the Diaphragm", "Stage I Supradiaphragmatic Lymphocyte-Depleted Classical Hodgkin Lymphoma", "Stage I Supradiaphragmatic Lymphocyte Depleted Classical Hodgkin Lymphoma", "Ann Arbor Stage I Supradiaphragmatic Lymphocyte-Depleted Classic Hodgkin Lymphoma", "Ann Arbor Stage I Supradiaphragmatic Lymphocyte-Depleted Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage I Supradiaphragmatic Lymphocyte-Depleted Classic Hodgkin Lymphoma", "shortest_name_length": 63}
{"curie": "UMLS:C1709664", "names": ["Primary Intraosseous Carcinoma Ex Keratocystic Odontogenic Tumor", "Primary Intraosseous Squamous Cell Carcinoma Derived From Keratocystic Odontogenic Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Intraosseous Squamous Cell Carcinoma Derived From Keratocystic Odontogenic Tumor", "shortest_name_length": 64}
{"curie": "MONDO:0022551", "names": ["Basedow's coma", "Coma basedovicum", "Karl Adolph von Basedow"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Basedow's coma", "shortest_name_length": 14}
{"curie": "MONDO:0015702", "names": ["CD45 deficiency", "T-B+ SCID due to CD45 deficiency", "T-B+ severe combined immunodeficiency due to CD45 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-B+ severe combined immunodeficiency due to CD45 deficiency", "shortest_name_length": 15}
{"curie": "MONDO:0004532", "names": ["auditory system cancer", "cancer of auditory system", "malignant auditory system neoplasm", "malignant neoplasm of auditory system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "auditory system cancer", "shortest_name_length": 22}
{"curie": "UMLS:C4055245", "names": ["Childhood Langerhans Cell Histiocytosis without Risk Organ Involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Langerhans Cell Histiocytosis without Risk Organ Involvement", "shortest_name_length": 70}
{"curie": "UMLS:C0149614", "names": ["Adnexal mass", "ADNEXAL MASS", "Adnexal Mass", "adnexal mass", "adnexal masses"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adnexal mass", "shortest_name_length": 12}
{"curie": "MONDO:0004884", "names": ["eye degenerative disease", "Eye degenerative disorder", "eye degenerative disorder", "degenerative disorder of eye", "Degenerative disorder of eye", "eye neurodegenerative disease", "Eye degenerative disorder NOS", "degenerative disorder of globe", "Degenerative disorder of globe", "degenerative disorders of globe", "Degenerative disorders of globe", "Degenerated conditions of globe", "Degenerative disorder of globe, NOS", "Degenerated globe or eye, unspecified", "Degenerative disorder of eye (disorder)", "Unspecified degenerative disorder of globe", "Degenerative disorder of globe, unspecified", "degenerative disorders of globe (diagnosis)", "eyeball of camera-type eye neurodegenerative disease", "neurodegenerative disease of eyeball of camera-type eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eye degenerative disorder", "shortest_name_length": 24}
{"curie": "UMLS:C4727003", "names": ["Unresectable Soft Tissue Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Soft Tissue Sarcoma", "shortest_name_length": 32}
{"curie": "MONDO:0019303", "names": ["Premature Aging", "Premature aging", "premature aging", "aging premature", "premature; aging", "Aging, Premature", "aging; premature", "Premature ageing", "premature ageing", "Premature aging syndrome", "premature aging syndrome", "syndrome premature aging", "Premature aging (finding)", "Premature ageing syndrome", "premature aging; presenile", "presenile; premature aging", "Physiologically old for age", "Premature aging syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "premature aging syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0021010", "names": ["skin lymphangiosarcoma", "Skin Lymphangiosarcoma", "Stewart Treves syndrome", "Stewart-Treves syndrome", "Lymphangiosarcoma of skin", "Lymphangiosarcoma of Skin", "lymphangiosarcoma of skin", "Lymphangiosarcoma of the Skin", "lymphangiosarcoma of the skin", "Stewart-Treves syndrome (disorder)", "Stewart-Treves syndrome (diagnosis)", "Postmastectomy extremity angiosarcoma", "Lymphangiosarcoma following mastectomy", "Lymphangiosarcoma of Stewart and Treves", "lymphangiosarcoma of Stewart and Treves", "Postmastectomy lymphangiosarcoma syndrome", "Angiosarcoma associated with chronic lymphedema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin lymphangiosarcoma", "shortest_name_length": 22}
{"curie": "UMLS:C4525894", "names": ["Stage III Pancreatic Neuroendocrine Tumor", "Stage III Pancreatic Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Pancreatic Neuroendocrine Tumor AJCC v8", "shortest_name_length": 41}
{"curie": "UMLS:C5419203", "names": ["Refractory Esophageal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Esophageal Carcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C1335695", "names": ["Recurrent Childhood Brainstem Astrocytoma", "Recurrent Childhood Brain Stem Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Brain Stem Astrocytoma", "shortest_name_length": 41}
{"curie": "MONDO:0020866", "names": ["diphtheria; nasopharynx", "Nasopharyngeal diphtheria", "Nasopharyngeal Diphtheria", "nasopharynx; diphtheritic", "nasopharyngeal diphtheria", "Diphtheria, nasopharyngeal", "Nasopharyngeal diphtheria (disorder)", "nasopharyngeal diphtheria (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasopharyngeal diphtheria", "shortest_name_length": 23}
{"curie": "UMLS:C5237053", "names": ["Recurrent Endometrial Dedifferentiated Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Endometrial Dedifferentiated Carcinoma", "shortest_name_length": 48}
{"curie": "UMLS:C0278865", "names": ["recurrent pituitary tumor", "Pituitary tumor recurrent", "pituitary tumor, recurrent", "Pituitary tumour recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pituitary tumor recurrent", "shortest_name_length": 25}
{"curie": "MONDO:0001985", "names": ["partial retinal artery occlusion", "Partial retinal artery occlusion", "retinal partial arterial occlusion", "Partial retinal arterial occlusion", "partial arterial retinal occlusion", "Partial arterial retinal occlusion", "Retinal partial arterial occlusion", "partial retinal arterial occlusion", "Partial Retinal Arterial Occlusion", "Partial occlusion of retinal artery", "partial retinal artery occlusion (diagnosis)", "Partial occlusion of retinal artery (disorder)", "Partial retinal artery occlusion, unspecified eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial arterial retinal occlusion", "shortest_name_length": 32}
{"curie": "MONDO:0003198", "names": ["Small Bowel Adenocarcinoma", "small bowel adenocarcinoma", "adenocarcinoma small bowel", "Small bowel adenocarcinoma", "adenocarcinoma bowel small", "Non-Ampullary Adenocarcinoma", "Adenocarcinoma of Small Bowel", "adenocarcinoma of small bowel", "adenocarcinoma intestine small", "Small intestine adenocarcinoma", "adenocarcinoma small intestine", "small intestine adenocarcinoma", "adenocarcinoma - small intest.", "Adenocarcinoma - small intest.", "Small Intestinal Adenocarcinoma", "small intestinal adenocarcinoma", "adenocarcinoma, small intestine", "adenocarcinoma of small intestine", "Adenocarcinoma of small intestine", "Adenocarcinoma of the Small Bowel", "adenocarcinoma of small Intestine", "Adenocarcinoma of Small Intestine", "Adenocarcinoma of the small bowel", "adenocarcinoma of the small bowel", "Small intestine adenocarcinoma NOS", "adenocarcinoma of small instestine", "Adenocarcinoma of the Small Intestine", "Adenocarcinoma of the small intestine", "adenocarcinoma of the small intestine", "adenocarcinoma of the small instestine", "Adenocarcinoma of small intestine (disorder)", "adenocarcinoma of small intestine (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small intestine adenocarcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0005215", "names": ["Vulva Cancer", "cancer vulva", "vulva cancer", "vulvar cancer", "Vulvar cancer", "cancer vulvar", "Vulvar Cancer", "Vulva Carcinoma", "carcinoma vulva", "vulva carcinoma", "Cancer of Vulva", "cancer of vulva", "vulvar carcinoma", "Vulvar Carcinoma", "Vulvar carcinoma", "carcinoma vulvar", "VULVA, CARCINOMA", "Carcinoma of vulva", "Carcinoma of Vulva", "carcinoma of vulva", "Vulvar cancer, NOS", "CARCINOMA OF VULVA", "cancer of the vulva", "Cancer of the Vulva", "Carcinoma of the Vulva", "carcinoma of the vulva", "VULVAR CANCER, CARCINOMA", "mammalian vulva carcinoma", "carcinoma of mammalian vulva", "carcinoma of vulva (diagnosis)", "Malignant epithelial neoplasm of vulva", "Malignant epithelial neoplasm of vulva (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar carcinoma", "shortest_name_length": 12}
{"curie": "MONDO:0007600", "names": ["FRTS1", "Primary Fanconi Syndrome", "primary Fanconi syndrome", "Fanconi renotubular syndrome 1", "primary Fanconi renotubular syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary Fanconi syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C4552673", "names": ["Stage I Ovarian Cancer", "Stage I Ovarian Cancer AJCC v8", "Stage I Ovarian Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Ovarian Cancer AJCC v8", "shortest_name_length": 22}
{"curie": "UMLS:C5206796", "names": ["Refractory Gallbladder Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Gallbladder Carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0013891", "names": ["ALS18", "ALS18 (diagnosis)", "AMYOTROPHIC LATERAL SCLEROSIS 18", "amyotrophic lateral sclerosis 18", "PFN1 amyotrophic lateral sclerosis", "amyotrophic lateral sclerosis ALS18", "amyotrophic lateral sclerosis type 18", "amyotrophic lateral sclerosis caused by mutation in PFN1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyotrophic lateral sclerosis type 18", "shortest_name_length": 5}
{"curie": "MONDO:0021416", "names": ["Gallbladder Polyp", "polyp gallbladder", "gallbladder polyp", "GALLBLADDER POLYP", "Gallbladder polyp", "gallbladders polyp", "gallbladder polyps", "gall bladder polyp", "polyps gallbladder", "gallbladders polyps", "Polyp of gallbladder", "polyp of gallbladder", "Polyp of Gallbladder", "Polyp(s);gallbladder", "polyp of the gallbladder", "Polyp of the Gallbladder", "gallbladder polyp (diagnosis)", "Gallbladder inflammatory polyp", "Polyp of gallbladder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyp of gallbladder", "shortest_name_length": 17}
{"curie": "MONDO:0019224", "names": ["disorder of GABA metabolism", "disorder of gamma-aminobutyric acid metabolism", "inborn disorder of gamma-aminobutyric acid metabolism", "inborn error of gamma-aminobutyric acid metabolic process", "inborn gamma-aminobutyric acid metabolic process disorder", "rare inborn error of gamma-aminobutyric acid metabolic process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of gamma-aminobutyric acid metabolism", "shortest_name_length": 27}
{"curie": "MONDO:0024889", "names": ["mesonephric adenoma", "Mesonephric adenoma", "Mesonephric Adenoma", "benign Mesonephroma", "Benign mesonephroma", "Benign Mesonephroma", "benign mesonephroma", "Mesonephroma, benign", "Wolffian Duct Adenoma", "Wolffian duct adenoma", "mesonephric duct adenoma", "benign mesonephric neoplasm", "mesonephric neoplasm, benign", "Mesonephroma, benign (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign mesonephroma", "shortest_name_length": 19}
{"curie": "MONDO:0019346", "names": ["ML I", "MUCOLIPIDOSIS I", "Sialidosis type 1", "sialidosis type I", "sialidosis type 1", "Normomorphic sialidosis", "normosomatic sialidosis", "lipomucopolysaccharidosis", "Lipomucopolysaccharidoses", "Lipomucopolysaccharidosis", "LIPOMUCOPOLYSACCHARIDOSIS", "Sialidosis type 1 (disorder)", "myoclonus cherry red spot syndrome", "cherry red spot myoclonus syndrome", "cherry-red spot-myoclonus syndrome", "Cherry red spot myoclonus syndrome", "Cherry-red spot-myoclonus syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sialidosis type 1", "shortest_name_length": 4}
{"curie": "MONDO:0700125", "names": ["chromosome 18 disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 18 disorder", "shortest_name_length": 22}
{"curie": "MONDO:0001280", "names": ["Choroiditis", "choroiditis", "CHOROIDITIS", "Choroiditides", "Choroiditis NOS", "Choroiditis, NOS", "Choroid inflamed", "Posterior Uveitis", "Posterior uveitis", "uveitis posterior", "posterior uveitis", "Uveitis, Posterior", "choroid; inflammation", "inflammation; choroid", "Choroiditis (disorder)", "Uveitis, posterior NOS", "Posterior uveitis, NOS", "choroiditis was present", "Inflammation of choroid", "uveal tract choroiditis", "choroiditis (diagnosis)", "posterior uveitis (disease)", "Posterior uveitis (disorder)", "Posterior uveitis (diagnosis)", "choroiditis (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choroiditis", "shortest_name_length": 11}
{"curie": "MONDO:0007056", "names": ["acroosteolysis", "Acroosteolysis", "ACROOSTEOLYSIS", "acro osteolysis", "Acro-Osteolysis", "Acro Osteolysis", "Acro-osteolysis", "acro-osteolysis", "Acroosteolysis, NOS", "Acroosteolysis Syndrome", "Acroosteolysis syndrome", "Acro-osteolysis syndrome", "Acro-Osteolysis Syndrome", "acro-osteolysis syndrome", "Acroosteolysis (disorder)", "Acro-Osteolysis Syndromes", "acroosteolysis (diagnosis)", "Breakdown of small bones of fingers", "Osteolytic defects of the phalanges of the hand"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acroosteolysis", "shortest_name_length": 14}
{"curie": "UMLS:C1708171", "names": ["Gallbladder Adenocarcinoma, Intestinal-Type", "intestinal type adenocarcinoma of gallbladder", "intestinal type adenocarcinoma of gallbladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intestinal type adenocarcinoma of gallbladder", "shortest_name_length": 43}
{"curie": "MONDO:0008343", "names": ["Pulmonary Atresia With Ventricular Septal Defect", "Pulmonary atresia with ventricular septal defect", "PULMONARY ATRESIA WITH VENTRICULAR SEPTAL DEFECT", "Pulmonary Atresia with Ventricular Septal Defect", "pulmonary atresia with ventricular septal defect", "Pulmonary Valve Atresia with Ventricular Septal Defect", "pulmonary valve atresia with ventricular septal defect", "PAVSD - Pulmonary atresia with ventricular septal defect", "Pulmonary atresia with ventricular septal defect (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary atresia with ventricular septal defect", "shortest_name_length": 48}
{"curie": "UMLS:C1881484", "names": ["Lung Mature B-Cell Neoplasm", "Lung Mature B-Cell Lymphocytic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Mature B-Cell Neoplasm", "shortest_name_length": 27}
{"curie": "MONDO:0010958", "names": ["LQT4", "LQT4 (diagnosis)", "long QT syndrome 4", "LONG QT SYNDROME 4", "Ankyrin-B Syndrome", "ANKYRIN-B SYNDROME", "ankyrin-B syndrome", "Long Qt Syndrome 4", "Ankyrin-B syndrome", "Cardiac arrhythmia ankyrin-B related", "ankyrin-B-related cardiac arrhythmia", "Cardiac Arrhythmia, Ankyrin-B-Related", "cardiac arrhythmia, ankyrin-b-related", "cardiac arrhythmia, ankyrin-B-related", "CARDIAC ARRHYTHMIA, ANKYRIN-B-RELATED", "Cardiac arrhythmia ankyrin-B related (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiac arrhythmia, ankyrin-B-related", "shortest_name_length": 4}
{"curie": "UMLS:C1336310", "names": ["Stage II Ovarian Yolk Sac Tumor", "Ovarian Yolk Sac Tumor Stage II", "Yolk Sac Tumor of Ovary Stage II", "Yolk Sac Tumor of the Ovary Stage II", "Stage II Ovarian Yolk Sac Tumor AJCC v7", "Stage II Ovarian Yolk Sac Tumor AJCC v6", "Stage II Ovarian Yolk Sac Tumor AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Ovarian Yolk Sac Tumor AJCC v6 and v7", "shortest_name_length": 31}
{"curie": "UMLS:C0521208", "names": ["Accident at home", "Household accident", "Accident at home, NOS", "Household accident, NOS", "Accident while engaged in household activity", "Accident whilst engaged in household activity", "ACCIDENTS WHILE ENGAGED IN HOUSEHOLD ACTIVITIES", "Accident while engaged in household activity, NOS", "Accident while engaged in household activity (event)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Accident while engaged in household activity", "shortest_name_length": 16}
{"curie": "MONDO:0012415", "names": ["PEOA4", "autosomal dominant progressive external ophthalmoplegia 4", "PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL DOMINANT 4", "progressive external ophthalmoplegia, autosomal dominant 4", "Progressive External Ophthalmoplegia, Autosomal Dominant, 4", "POLG2 progressive external ophthalmoplegia with mitochondrial DNA deletions", "autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4", "PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 4", "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4", "Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 4", "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant type 4", "progressive external ophthalmoplegia with mitochondrial DNA deletions caused by mutation in POLG2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4", "shortest_name_length": 5}
{"curie": "MONDO:0010627", "names": ["XLP", "XLP1", "Duncan disease", "Duncan Disease", "Duncan syndrome", "duncan syndrome", "Disease, Duncan", "Purtilo Syndrome", "Purtilo syndrome", "duncans syndrome", "duncan's syndrome", "Duncan's Syndrome", "Duncan's syndrome", "Syndrome, Purtilo", "Purtilo Syndromes", "Syndromes, Purtilo", "Immunodeficiency 5", "Immunodeficiency 5s", "Fatal Epstein-Barr virus syndrome", "x-linked lymphoproliferative disease", "X-Linked Lymphoproliferative Disease", "X Linked Lymphoproliferative Disease", "X-linked lymphoproliferative disease", "Lymphoproliferative Disease, X-Linked", "Disease, X-Linked Lymphoproliferative", "Familial Fatal Epstein Barr Infection", "X Linked Lymphoproliferative Syndrome", "X-linked lymphoproliferative syndrome", "X linked lymphoproliferative syndrome", "X-Linked Lymphoproliferative Disorder", "X Linked Lymphoproliferative Disorder", "X-Linked Lymphoproliferative Diseases", "Familial fatal Epstein-Barr infection", "Lymphoproliferative Disease, X Linked", "X-Linked Lymphoproliferative Syndrome", "Familial Fatal Epstein-Barr Infection", "X-linked Lymphoproliferative Syndrome", "lymphoproliferative syndrome, X-linked", "Syndrome, X-Linked Lymphoproliferative", "Lymphoproliferative Syndrome, X-Linked", "lymphoproliferative; disease, X-linked", "Lymphoproliferative Diseases, X-Linked", "Lymphoproliferative Disorder, X-Linked", "Diseases, X-Linked Lymphoproliferative", "X-Linked Lymphoproliferative Disorders", "X-Linked Lymphoproliferative Syndromes", "Disorder, X-Linked Lymphoproliferative", "Disorders, X-Linked Lymphoproliferative", "X-linked lymphoproliferative syndrome 1", "Syndromes, X-Linked Lymphoproliferative", "lymphoproliferative syndrome X-linked 1", "EBV - Fatal Epstein-Barr virus syndrome", "Lymphoproliferative Disorders, X-Linked", "Lymphoproliferative Syndromes, X-Linked", "Lymphoproliferative Syndrome, X-Linked, 1", "lymphoproliferative syndrome, X-linked, 1", "X-linked lymphoproliferative syndrome type 1", "Epstein Barr Virus Infection, Familial Fatal", "Epstein-Barr Virus Infection, Familial Fatal", "XLPS - X-linked lymphoproliferative syndrome", "lymphoproliferative syndrome, X-linked, type 1", "Severe susceptibility to Epstein-Barr infection", "x-linked lymphoproliferative disease (diagnosis)", "X-linked lymphoproliferative syndrome (disorder)", "SH2D1A-related lymphoproliferative disease, X-linked", "disease (or disorder); lymphoproliferative, X-linked", "Immunodeficiency, X Linked Progressive Combined Variable", "Immunodeficiency, X-Linked Progressive Combined Variable", "Epstein Barr Virus Induced Lymphoproliferative Disease In Males", "Epstein-Barr Virus-Induced Lymphoproliferative Disease In Males"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked lymphoproliferative syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0015176", "names": ["undetermined colitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "undetermined colitis", "shortest_name_length": 20}
{"curie": "UMLS:C2721563", "names": ["Infectious pneumonitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infectious pneumonitis", "shortest_name_length": 22}
{"curie": "UMLS:C0263978", "names": ["Soft Tissue Disease", "Soft Tissue Disorder", "Soft tissue disorder", "Soft Tissue Diseases", "Soft tissue disorders", "soft tissue; disorder", "Soft Tissue Disorders", "Disorder of soft tissue", "Soft tissue disorder NOS", "Disorder of soft tissue, NOS", "Unspecified soft tissue disorder", "Soft tissue disorder, unspecified", "disease (or disorder); soft tissue", "Disorder of soft tissue (disorder)", "unspecified disorder of soft tissue", "Disorders of soft tissue, unspecified", "unspecified disorder of soft tissue (diagnosis)", "Unspecified soft tissue disorder, site unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disorder of soft tissue", "shortest_name_length": 19}
{"curie": "UMLS:C3805015", "names": ["Stoma site hemorrhage", "Stoma site haemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stoma site hemorrhage", "shortest_name_length": 21}
{"curie": "OMIM:618983", "names": ["LEWIS-NEGATIVE PHENOTYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 24}
{"curie": "MONDO:0016561", "names": ["Del(1)(q44)", "monosomy 1q44", "Monosomy 1q44", "1q44 microdeletion syndrome", "chromosome 1q44 microdeletion syndrome", "1q44 microdeletion syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "1q44 microdeletion syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0015819", "names": ["indolent primary cutaneous B-cell lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "indolent primary cutaneous B-cell lymphoma", "shortest_name_length": 42}
{"curie": "MONDO:0000190", "names": ["VF", "vf", "VFib", "FIBRILLATION VENTRICULAR", "VENTRICULAR FIBRILLATION", "Fibrillation;ventricular", "ventricular fibrillation", "Ventricular Fibrillation", "fibrillation ventricular", "Ventricular fibrillation", "Fibrillation ventricular", "Fibrillation, Ventricular", "ventricular; fibrillation", "fibrillation, ventricular", "Ventricular Fibrillations", "fibrillation; ventricular", "Fibrillations, Ventricular", "FIBRILLATION PAROXYSMAL VENT", "Fibrillation paroxysmal vent", "VF - Ventricular fibrillation", "VENTRICULAR FIBRILLATION PAROXYSM", "Ventricular fibrillation paroxysm", "ventricular fibrillation (disease)", "Ventricular fibrillation (disorder)", "Paroxysmal ventricular fibrillation", "Ventricular fibrillation paroxysmal", "ventricular fibrillation (diagnosis)", "Cardiac arrest - ventricular fibrillation", "Cardiac arrest and ventricular fibrillation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ventricular fibrillation", "shortest_name_length": 2}
{"curie": "MONDO:0032569", "names": ["CPHD7", "IGHD5", "IGHD5, FORMERLY", "ISOLATED GROWTH HORMONE DEFICIENCY, TYPE V", "isolated growth hormone deficiency, type 5", "ISOLATED GROWTH HORMONE DEFICIENCY, TYPE V, FORMERLY", "PITUITARY HORMONE DEFICIENCY, COMBINED OR ISOLATED, 7", "pituitary hormone deficiency, combined or isolated, 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated growth hormone deficiency, type 5", "shortest_name_length": 5}
{"curie": "MONDO:0003055", "names": ["Secretory Meningioma", "secretory meningioma", "Secretory meningioma", "Secretory Meningiomas", "Meningioma, Secretory", "Meningiomas, Secretory", "Secretory meningioma (morphologic abnormality)", "secretory meningioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secretory meningioma", "shortest_name_length": 20}
{"curie": "MONDO:0023050", "names": ["Van Den Ende Brunner syndrome", "Ectrodactyly cardiopathy dysmorphism", "ectrodactyly cardiopathy dysmorphism", "Ectrodactyly of lower limbs, congenital heart defect and characteristic facies", "ectrodactyly of lower limbs, congenital heart defect and characteristic facies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectrodactyly cardiopathy dysmorphism", "shortest_name_length": 29}
{"curie": "MONDO:0008583", "names": ["torticollis", "fibromatosis colli", "Fibromatosis Colli", "Fibromatosis colli", "congenital wryneck", "Congenital wryneck", "Congenital wry neck", "congenital wry neck", "familial torticollis", "torticollis, familial", "inherited torticollis", "torticollis congenital", "Congenital torticollis", "congenital torticollis", "torticollis; congenital", "Torticollis, congenital", "congenital; torticollis", "torticollis, congenital", "Fibromatosis colli (disorder)", "Fibromatosis colli of infancy", "Fibromatosis colli (diagnosis)", "familial spasmodic torticollis", "Congenital Muscular Torticollis", "inherited torticollis (disease)", "Congenital muscular torticollis", "congenital muscular torticollis", "sternocleidomastoid; contracture", "contracture; sternocleidomastoid", "Congenital torticollis (disorder)", "congenital torticollis (diagnosis)", "congenital sternomastoid torticollis", "Congenital sternomastoid torticollis", "Sternocleidomastoid tumor of infancy", "Sternocleidomastoid tumour of infancy", "Congenital (sternomastoid) torticollis", "contracture of sternocleidomastoid muscle", "Contracture of sternocleidomastoid muscle", "Congenital contracture of sternocleidomastoid", "soft tissue neoplasm benign - fibromatosis colli", "Congenital contracture of sternocleidomastoid muscle", "Congenital contracture of sternocleidomastoid (muscle)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited torticollis", "shortest_name_length": 11}
{"curie": "MONDO:0019327", "names": ["phakomatosis spilorosea", "Phakomatosis spilorosea", "Phakomatosis spilorosea (disorder)", "Phakomatosis pigmentovascularis type 3", "phakomatosis pigmentovascularis type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phakomatosis spilorosea", "shortest_name_length": 23}
{"curie": "UMLS:C1828079", "names": ["Dementia with Parkinsonism", "dementia parkinson's disease", "Parkinson's disease dementia", "dementia disease parkinson's", "Dementia in Parkinsons disease", "Dementia in Parkinson's disease", "dementia in parkinson's disease", "Parkinson disease with dementia", "Dementia associated with Parkinson Disease", "Parkinson disease with dementia (diagnosis)", "Dementia associated with Parkinson's Disease", "Dementia associated with Parkinson's Disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dementia associated with Parkinson's Disease", "shortest_name_length": 26}
{"curie": "MONDO:0018064", "names": ["Hunter Rudd Hoffmann syndrome", "Hunter-Rudd-Hoffmann syndrome", "trigonocephaly-broad thumbs syndrome", "Trigonocephaly-broad thumbs syndrome", "Trigonocephaly with broad thumb syndrome", "Trigonocephaly with broad thumb syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trigonocephaly-broad thumbs syndrome", "shortest_name_length": 29}
{"curie": "MONDO:0020711", "names": ["PerRTH", "selective peripheral resistance to thyroid hormone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "selective peripheral resistance to thyroid hormone", "shortest_name_length": 6}
{"curie": "MONDO:0013280", "names": ["MLPS", "MRCLS", "myxoliposarcoma", "Myxoliposarcoma", "liposarcoma myxoid", "Myxoid liposarcoma", "myxoid liposarcoma", "MYXOID LIPOSARCOMA", "Myxoid Liposarcoma", "Myxoid Liposarcomas", "myxoid; liposarcoma", "liposarcoma; myxoid", "Liposarcoma, Myxoid", "Liposarcomas, Myxoid", "Embryonal liposarcoma", "mixed-type liposarcoma", "Round Cell Liposarcoma", "liposarcoma; embryonal", "embryonal; liposarcoma", "mixed type liposarcoma", "Mixed type liposarcoma", "Round Cell Liposarcomas", "liposarcoma; mixed type", "Liposarcoma, Round Cell", "mixed; liposarcoma (type)", "cellular myxoid liposarcoma", "Myxoid liposarcoma (disorder)", "myxoid/round cell liposarcoma", "Myxoid/round cell liposarcoma", "Myxoid/Round Cell Liposarcoma", "myxoid liposarcoma (diagnosis)", "mixed type liposarcoma (diagnosis)", "Myxoid liposarcoma (morphologic abnormality)", "myxoid liposarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myxoid liposarcoma", "shortest_name_length": 4}
{"curie": "UMLS:C3544078", "names": ["Neuroendocrine breast tumor", "Breast Neuroendocrine Tumor", "Neuroendocrine breast tumour"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neuroendocrine breast tumor", "shortest_name_length": 27}
{"curie": "MONDO:0019320", "names": ["acanthokeratolytic verrucous nevus", "verrucous nevus acanthokeratolytic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acanthokeratolytic verrucous nevus", "shortest_name_length": 34}
{"curie": "MONDO:0010258", "names": ["MEHMO", "MRXS25", "MRXS20", "MRXSBRK", "MEHMO SYNDROME", "MEHMO syndrome", "X-linked MEHMO syndrome", "MEHMO syndrome, X-linked recessive", "syndromic X-linked mental retardation 25", "syndromic X-linked mental retardation 20", "MENTAL RETARDATION, X-LINKED, SYNDROMIC 25", "mental retardation, X-linked, syndromic 25", "MENTAL RETARDATION, X-LINKED, SYNDROMIC 20", "mental retardation, X-linked, syndromic 20", "syndromic X-linked intellectual disability 20", "syndromic X-linked intellectual disability 25", "intellectual disability, X-linked, syndromic 25", "intellectual disability, X-linked, syndromic 20", "mental retardation, X-linked, syndromic, Borck type", "MENTAL RETARDATION, X-LINKED, SYNDROMIC, BORCK TYPE", "intellectual disability, X-linked, syndromic, Borck type", "intellectual disability, X-linked, syndromic, Borck type; MRXSBRK", "X-linked intellectual disability-epileptic seizures-hypogenitalism-microcephaly-obesity syndrome", "MENTAL RETARDATION, EPILEPTIC SEIZURES, HYPOGONADISM AND HYPOGENITALISM, MICROCEPHALY, AND OBESITY", "mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, and obesity", "Mental Retardation, Epileptic Seizures, Hypogonadism and Hypogenitalism, Microcephaly, and Obesity", "intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, and obesity", "Mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome", "Intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome", "MEHMO (mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity) syndrome", "X-linked intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome", "Intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome (disorder)", "Intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MEHMO syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0020837", "names": ["OOMD5", "oocyte maturation defect 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oocyte maturation defect 5", "shortest_name_length": 5}
{"curie": "MONDO:0020127", "names": ["genetic peripheral neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genetic peripheral neuropathy", "shortest_name_length": 29}
{"curie": "MONDO:0015432", "names": ["R12", "Ring 12", "ring chromosome 12", "chromosome 12 ring", "Chromosome 12 ring", "Ring Chromosome 12", "Ring chromosome 12", "Ring chromosome type 12", "Ring chromosome 12 syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ring chromosome 12", "shortest_name_length": 3}
{"curie": "UMLS:C1142487", "names": ["Intestinal Stoma Obstruction", "intestinal stoma obstruction", "Intestinal stoma obstruction", "intestinal stoma obstruction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal Stoma Obstruction", "shortest_name_length": 28}
{"curie": "MONDO:0013914", "names": ["FIGD", "HH12", "eunuchoidism familial hypogonadotropic", "familial hypogonadotropic eunuchoidism", "eunuchoidism, familial hypogonadotropic", "Eunuchoidism, familial hypogonadotropic", "familial hypogonadotrophic eunuchoidism", "EUNUCHOIDISM, FAMILIAL HYPOGONADOTROPIC", "familial idiopathic gonadotrpin deficiency", "gonadotropin deficiency familial idiopathic", "Gonadotropin deficiency, familial idiopathic", "GONADOTROPIN DEFICIENCY, FAMILIAL IDIOPATHIC", "gonadotropin deficiency, familial idiopathic", "HYPOGONADOTROPIC HYPOGONADISM 12 WITH OR WITHOUT ANOSMIA", "hypogonadotropic hypogonadism 12 with or without anosmia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadotropic hypogonadism 12 with or without anosmia", "shortest_name_length": 4}
{"curie": "UMLS:C1262168", "names": ["Cholecystitis infective"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cholecystitis infective", "shortest_name_length": 23}
{"curie": "UMLS:C1710139", "names": ["Sparsely Granulated Lactotroph PitNET/Adenoma", "Sparsely Granulated Pituitary Gland Lactotroph Adenoma", "Sparsely Granulated Lactotroph Pituitary Neuroendocrine Tumor", "Sparsely Granulated Lactotroph Pituitary Neuroendocrine Tumor/Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sparsely Granulated Lactotroph Pituitary Neuroendocrine Tumor", "shortest_name_length": 45}
{"curie": "MONDO:0600014", "names": ["ACD without misalignment", "alveolar capillary dysplasia without misalignment of pulmonary veins"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alveolar capillary dysplasia without misalignment of pulmonary veins", "shortest_name_length": 24}
{"curie": "MONDO:0004591", "names": ["impetigo herpetiformis", "Impetigo herpetiformis", "herpetiformis; impetigo", "impetigo; herpetiformis", "impetigo herpetiformis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "impetigo herpetiformis", "shortest_name_length": 22}
{"curie": "MONDO:0000563", "names": ["GRID2-related spinocerebellar ataxia", "GRID2-related autosomal dominant spinocerebellar ataxia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "GRID2-related autosomal dominant spinocerebellar ataxia", "shortest_name_length": 36}
{"curie": "MONDO:0015830", "names": ["partial bilateral aplasia of the mullerian ducts", "partial bilateral aplasia of the Müllerian ducts", "incomplete bilateral aplasia of the Mullerian ducts", "incomplete bilateral aplasia of the Müllerian ducts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial bilateral aplasia of the mullerian ducts", "shortest_name_length": 48}
{"curie": "UMLS:C0272753", "names": ["Femur shaft fracture", "femur shaft fracture", "Fracture;femur;shaft", "femoral fracture shaft", "Femoral Shaft Fracture", "fracture; femur, shaft", "femoral shaft fracture", "femoral fractures shaft", "fracture of shaft of femur", "Fracture of shaft of femur", "Fracture of shaft of femur (disorder)", "fracture of shaft of femur (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fracture of shaft of femur", "shortest_name_length": 20}
{"curie": "MONDO:0032792", "names": ["CMT6C", "CMT 6C", "HMSN6C", "HMSN 6C", "HMSN VIC", "Charcot-Marie-Tooth Disease, Type 6C", "CHARCOT-MARIE-TOOTH DISEASE, TYPE 6C", "NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIC, WITH OPTIC ATROPHY", "neuropathy, hereditary motor and sensory, type VIc, with optic atrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuropathy, hereditary motor and sensory, type VIc, with optic atrophy", "shortest_name_length": 5}
{"curie": "MONDO:0020856", "names": ["BMFS4", "BONE MARROW FAILURE SYNDROME 4", "bone marrow failure syndrome 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bone marrow failure syndrome 4", "shortest_name_length": 5}
{"curie": "UMLS:C3897239", "names": ["Untreated Anaplastic Astrocytoma", "untreated childhood anaplastic astrocytoma", "Untreated Childhood Anaplastic Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Untreated Childhood Anaplastic Astrocytoma", "shortest_name_length": 32}
{"curie": "MONDO:0020462", "names": ["tarsal kink syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tarsal kink syndrome", "shortest_name_length": 20}
{"curie": "MONDO:0003904", "names": ["Occult Lung Squamous Cell Carcinoma", "Occult Squamous Cell Lung Carcinoma", "lung occult squamous cell carcinoma", "occult squamous cell lung carcinoma", "occult squamous cell carcinoma of lung", "Occult Squamous Cell Carcinoma of Lung", "Occult Squamous Cell Carcinoma of the Lung", "Occult squamous cell carcinoma of the lung", "occult squamous cell carcinoma of the lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung occult squamous cell carcinoma", "shortest_name_length": 35}
{"curie": "MONDO:0002418", "names": ["Ethmoid Sinus Adenocarcinoma", "ethmoid sinus adenocarcinoma", "adenocarcinoma of ethmoid sinus", "Adenocarcinoma of Ethmoid Sinus", "Adenocarcinoma of the Ethmoid Sinus", "adenocarcinoma of the ethmoid sinus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ethmoid sinus adenocarcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0004736", "names": ["aminoacidopathy", "AMINOACIDOPATHY", "amino acidopathy", "Amino acidopathy", "aminoacidopathies", "Hyperaminoaciduria", "Amino Acidopathies", "amino acidopathies", "amino acid disorder", "hyperaminoacidurias", "Amino acid disorder", "acid amino disorder", "disorder; amino-acid", "acid amino disorders", "acids amino disorder", "Amino acidopathy, NOS", "Inborn Amino Acidopathy", "Hyperaminoaciduria, NOS", "Amino acid disorder, NOS", "Amino Acidopathy, Inborn", "Inborn Amino Acidopathies", "Amino Acidopathies, Inborn", "Congenital Amino Acidopathy", "Amino Acidopathy, Congenital", "Congenital Amino Acidopathies", "amino acid metabolic disorder", "amino-acid metabolic disorder", "Disorder;amino-acid metabolic", "Amino Acid Metabolism Disorder", "Amino Acidopathies, Congenital", "metabolic disorder; amino-acid", "Amino acid metabolism disorder", "amino acid metabolism disorder", "amino-acid; metabolic disorder", "amino-acid metabolism disorder", "acid amino disorders metabolism", "amino acid metabolism disorders", "disorder; amino-acid metabolism", "Amino Acid Metabolism Disorders", "Disorder of amino acid metabolism", "Disorder of Amino Acid Metabolism", "Amino acids--Metabolism--Disorders", "DISORDERS OF AMINO ACID METABOLISM", "disorders of amino acid metabolism", "Amino Acid Metabolism, Inborn Error", "amino acid metabolism, inborn errors", "Inborn Errors, Amino Acid Metabolism", "inborn aminoacid metabolism disorder", "Amino Acid Metabolism, Inborn Errors", "inborn amino acid metabolism disorder", "INBORN ERROR OF AMINO ACID METABOLISM", "Inborn error of amino acid metabolism", "inborn error of amino acid metabolism", "Disorder of amino acid metabolism, NOS", "inborn errors of amino acid metabolism", "Inborn errors of amino acid metabolism", "Amino acid metabolism, Inborn errors of", "inherited amino acid metabolic disorder", "Amino Acid Metabolism Disorders, Inborn", "inborn disorder of amino acid metabolism", "amino-acid metabolism disorder (diagnosis)", "Inborn error of amino acid metabolism, NOS", "Disorder of amino acid metabolism (disorder)", "Unspecified disorder of amino-acid metabolism", "Disorder of amino-acid metabolism, unspecified", "Disorder of amino acid transport and metabolism", "Disorders of amino-acid transport and metabolism", "Disorders of amino acid transport and metabolism", "Inborn error of amino acid metabolism (disorder)", "inborn cellular amino acid metabolic process disorder", "inborn error of cellular amino acid metabolic process", "rare inborn error of cellular amino acid metabolic process", "Disorders of amino acid transport and metabolism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of amino acid metabolism", "shortest_name_length": 15}
{"curie": "UMLS:C0338642", "names": ["Toxic confusional state", "delirium confusional state toxic", "Toxic confusional state (disorder)", "Toxic confusional state (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Toxic confusional state", "shortest_name_length": 23}
{"curie": "UMLS:C5556679", "names": ["Advanced Thymic Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Thymic Neuroendocrine Neoplasm", "shortest_name_length": 39}
{"curie": "MONDO:0007424", "names": ["DFNA1", "LFHL1", "Konigsmark syndrome", "KONIGSMARK SYNDROME", "Konigsmark Syndrome", "autosomal dominant deafness 1", "DEAFNESS, AUTOSOMAL DOMINANT 1", "deafness, progressive Low tone", "Deafness, Progressive Low Tone", "deafness, autosomal dominant 1", "Deafness, Autosomal Dominant 1", "deafness, autosomal dominant type 1", "hereditary Low frequency hearing loss", "Hereditary Low Frequency Hearing Loss", "hereditary low frequency hearing loss 1", "autosomal dominant nonsyndromic deafness 1", "autosomal dominant nonsyndromic hearing loss 1", "DIAPH1 autosomal dominant nonsyndromic deafness", "autosomal dominant nonsyndromic deafness type 1", "DIAPH1-related sensorineural deafness-thrombocytopenia syndrome", "autosomal dominant deafness 1, with or without thrombocytopenia", "DEAFNESS, AUTOSOMAL DOMINANT 1, WITH OR WITHOUT THROMBOCYTOPENIA", "deafness, autosomal dominant 1, with or without thrombocytopenia", "DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome", "autosomal dominant nonsyndromic deafness caused by mutation in DIAPH1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 1", "shortest_name_length": 5}
{"curie": "MONDO:0044983", "names": ["Benign lipomatous tumor", "benign lipomatous tumor", "lipomatous tumor benign", "Benign Lipomatous Tumor", "Benign lipomatous tumour", "Benign lipomatous neoplasm", "benign lipomatous neoplasm", "Benign Lipomatous Neoplasm", "benign adipose tissue tumor", "Benign Adipose Tissue Tumor", "Benign Tumor of Adipose Tissue", "benign tumor of adipose tissue", "benign adipose tissue neoplasm", "Benign Adipose Tissue Neoplasm", "benign neoplasm of adipose tissue", "Benign Neoplasm of Adipose Tissue", "benign tumor of the adipose tissue", "Benign lipomatous tumor (disorder)", "Benign Tumor of the Adipose Tissue", "benign lipomatous tumor (diagnosis)", "Benign Neoplasm of the Adipose Tissue", "benign neoplasm of the adipose tissue", "Benign lipomatous neoplasm, unspecified", "adipose tissue benign connective and soft tissue neoplasm", "benign connective and soft tissue neoplasm of adipose tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign lipomatous neoplasm", "shortest_name_length": 23}
{"curie": "MONDO:0013814", "names": ["PDCOS", "PODOCONIOSIS, SUSCEPTIBILITY TO", "podoconiosis, susceptibility to", "LYMPHOSTATIC VERRUCOSIS, SUSCEPTIBILITY TO", "lymphostatic verrucosis, susceptibility to", "endemic Nonfilarial elephantiasis, susceptibility to", "ENDEMIC NONFILARIAL ELEPHANTIASIS, SUSCEPTIBILITY TO", "Nonfilarial elephantiasis of Lower legs, susceptibility to", "NONFILARIAL ELEPHANTIASIS OF LOWER LEGS, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "podoconiosis, susceptibility to", "shortest_name_length": 5}
{"curie": "MONDO:0019254", "names": ["purine-pyrimidine metabolic disorder", "purine/pyrimidine metabolism disorder", "Purine and pyrimidine metabolism disorder", "Purine and pyrimidine metabolism disorders", "inborn purine-pyrimidine metabolic disorder", "Purine-Pyrimidine Metabolism, Inborn Errors", "Purine Pyrimidine Metabolism, Inborn Errors", "disorder of purine or pyrimidine metabolism", "Disorder of purine or pyrimidine metabolism", "Disorder of purine and pyrimidine metabolism", "disorders of purine and pyrimidine metabolism", "DISORDERS OF PURINE AND PYRIMIDINE METABOLISM", "inborn errors of purine-pyrimidine metabolism", "Disorders of purine and pyrimidine metabolism", "inborn disorder of purine or pyrimidine metabolism", "Other disorders of purine and pyrimidine metabolism", "Disorder of purine and pyrimidine metabolism (disorder)", "disorders of purine and pyrimidine metabolism (diagnosis)", "Disorder of purine and pyrimidine metabolism, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of purine or pyrimidine metabolism", "shortest_name_length": 36}
{"curie": "MONDO:0015749", "names": ["Del(6)(q16)", "monosomy 6q16", "6q16 deletion syndrome", "Prader-Willi-like syndrome due to deletion 6q16"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "6q16 deletion syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0001843", "names": ["Intramural uterine fibroid", "intramural uterine leiomyoma", "Interstitial uterine fibroid", "UTERINE LEIOMYOMA INTRAMURAL", "Intramural uterine leiomyoma", "uterus interstitial leiomyoma", "uterus; leiomyoma, intramural", "leiomyoma; uterus, intramural", "Intramural leiomyoma of uterus", "intramural leiomyoma of uterus", "Interstitial leiomyoma of uterus", "Intramural leiomyoma of uterus (disorder)", "intramural leiomyoma of uterus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterus interstitial leiomyoma", "shortest_name_length": 26}
{"curie": "UMLS:C4527177", "names": ["Stage I Cutaneous (Skin) Melanoma", "Pathologic Stage I Cutaneous Melanoma AJCC v8", "Pathologic Stage I Melanoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage I Cutaneous Melanoma AJCC v8", "shortest_name_length": 33}
{"curie": "MONDO:0005449", "names": ["conduction system disorder", "conducting system of heart disease", "disease of conducting system of heart", "disorder of conducting system of heart", "conducting system of heart disease or disorder", "disease or disorder of conducting system of heart"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "conduction system disorder", "shortest_name_length": 26}
{"curie": "UMLS:C1334593", "names": ["Intracranial Cancer", "Malignant Intracranial Tumor", "Intracranial Tumors, Malignant", "Malignant Intracranial Neoplasm", "Intracranial Neoplasms, Malignant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Intracranial Neoplasm", "shortest_name_length": 19}
{"curie": "UMLS:C0234299", "names": ["Primary salt taste disorder", "Taste disorder, primary, salt", "Taste Disorder, Primary, Salt", "Primary salt taste disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Taste Disorder, Primary, Salt", "shortest_name_length": 27}
{"curie": "MONDO:0030423", "names": ["CDG2V", "congenital disorder of glycosylation, type 2v", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE 2v"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital disorder of glycosylation, type 2v", "shortest_name_length": 5}
{"curie": "MONDO:0014311", "names": ["SCAR15", "Salih ataxia", "SALIH ATAXIA", "autosomal recessive spinocerebellar ataxia 15", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 15", "spinocerebellar ataxia, autosomal recessive 15", "Autosomal recessive spinocerebellar ataxia type 15", "autosomal recessive spinocerebellar ataxia type 15", "spinocerebellar ataxia, autosomal recessive type 15", "SCAR15 - autosomal recessive spinocerebellar ataxia type 15", "RUBCN autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome", "RUBCN autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome", "Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN deficiency", "autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN deficiency", "Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to RUBCN deficiency", "autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome caused by mutation in RUBCN", "autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome due to KIAA0226 deficiency", "autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome caused by mutation in RUBCN", "Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to RUN and cysteine rich domain containing beclin 1 interacting protein deficiency", "Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN (RUN and cysteine rich domain containing beclin 1 interacting protein) deficiency", "Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to RUN and cysteine rich domain containing beclin 1 interacting protein deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive spinocerebellar ataxia 15", "shortest_name_length": 6}
{"curie": "UMLS:C2984117", "names": ["Sinonasal Cancer by AJCC v7 Stage", "Sinonasal Carcinoma by AJCC v7 Stage", "Nasal Cavity and Paranasal Sinus Cancer by AJCC v7 Stage", "Nasal Cavity and Paranasal Sinus Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Cancer by AJCC v7 Stage", "shortest_name_length": 33}
{"curie": "MONDO:0021467", "names": ["benign renal pelvis tumor", "Benign Renal Pelvis Tumor", "Benign Renal Pelvis Neoplasm", "benign renal pelvis neoplasm", "Benign tumor of renal pelvis", "benign tumor of renal pelvis", "renal pelvis benign neoplasm", "Benign Tumor of Renal Pelvis", "benign kidney pelvis neoplasm", "Benign Kidney Pelvis Neoplasm", "Benign tumour of renal pelvis", "Benign Neoplasm of Renal Pelvis", "benign neoplasm of renal pelvis", "Benign neoplasm of renal pelvis", "benign tumor of the renal pelvis", "Benign Tumor of the Renal Pelvis", "benign neoplasm of the renal pelvis", "Benign Neoplasm of the Renal Pelvis", "Benign neoplasm of renal pelvis (disorder)", "benign neoplasm of renal pelvis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of renal pelvis", "shortest_name_length": 25}
{"curie": "MONDO:0007902", "names": ["Lichen Planus, Familial", "lichen planus, familial", "LICHEN PLANUS, FAMILIAL", "hereditary lichen planus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lichen planus, familial", "shortest_name_length": 23}
{"curie": "UMLS:C1512749", "names": ["Urothelial carcinoma with trophoblastic differentiation", "Infiltrating Bladder Urothelial Carcinoma with Trophoblastic Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infiltrating Bladder Urothelial Carcinoma with Trophoblastic Differentiation", "shortest_name_length": 55}
{"curie": "UMLS:C5556739", "names": ["Vaginal Mucinous Adenocarcinoma, Gastric-Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Mucinous Adenocarcinoma, Gastric-Type", "shortest_name_length": 45}
{"curie": "MONDO:0021053", "names": ["CBT1", "Chemodectoma", "chemodectoma", "CHEMODECTOMAS", "Chemodectomas", "carotid body tumor", "Carotid Body Tumor", "Carotid body tumor", "carotid body tumors", "tumor; carotid body", "Carotid Body Tumors", "carotid body tumour", "Carotid body tumour", "CAROTID BODY, TUMOR", "Carotid body tumors", "Tumor, Carotid Body", "CAROTID BODY TUMORS", "body carotid tumours", "Carotid body tumours", "Tumors, Carotid Body", "Carotid body--Tumors", "Tumor of Carotid Body", "tumor of carotid body", "[M]Carotid body tumor", "[M]Carotid body tumour", "Glomus caroticum tumor", "Glomus caroticum tumour", "Neoplasm of carotid body", "Carotid Body Chemodectoma", "carotid body chemodectoma", "Tumor of the Carotid Body", "tumor of the carotid body", "chemodectoma, undetermined", "Carotid Body Paraganglioma", "Carotid body paraganglioma", "paraganglioma carotid body", "carotid body paraganglioma", "paraganglioma; carotid body", "PARAGANGLIOMA, CAROTID BODY", "Paraganglioma, Carotid Body", "Carotid Body Paragangliomas", "Paragangliomas, Carotid Body", "Paraganglioma of Carotid Body", "paraganglioma of carotid body", "carotid body tumor (diagnosis)", "Paraganglioma of the Carotid Body", "paraganglioma of the carotid body", "Neoplasm of carotid body (disorder)", "Carotid body tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carotid body paraganglioma", "shortest_name_length": 4}
{"curie": "MONDO:0023692", "names": ["MSUD type IB", "MSUD type 3 (formerly)", "maple syrup urine disease type 1B", "MSUD due to deficiency of E1-beta subunit of branched-chain alpha-keto acid dehydrogenase complex"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maple syrup urine disease type 1B", "shortest_name_length": 12}
{"curie": "MONDO:0016756", "names": ["inherited nervous system cancer-predisposing syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited nervous system cancer-predisposing syndrome", "shortest_name_length": 53}
{"curie": "UMLS:C5446455", "names": ["Lacrimal Drainage System Melanoma", "Melanoma of the Lacrimal Drainage System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lacrimal Drainage System Melanoma", "shortest_name_length": 33}
{"curie": "UMLS:C0558401", "names": ["SKIN LACERATION", "skin laceration", "Skin laceration", "laceration skin", "lacerations skin", "Laceration of skin", "laceration of skin", "Injury;laceration;skin", "Laceration of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin laceration", "shortest_name_length": 15}
{"curie": "MONDO:0018843", "names": ["embryonal carcinoma", "embryonal carcinoma of CNS", "Embryonal Carcinoma of CNS", "Embryonal carcinoma of CNS", "Embryonal carcinoma of the CNS", "embryonal carcinoma of the CNS", "central nervous system embryonal carcinoma", "Central Nervous System Embryonal Carcinoma", "Embryonal Carcinoma of the Central Nervous System", "embryonal carcinoma of the central nervous system", "Embryonal carcinoma of the central nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "embryonal carcinoma of the central nervous system", "shortest_name_length": 19}
{"curie": "UMLS:C1336353", "names": ["Stage IVA Mouth Epidermoid Carcinoma", "Stage IVA Mouth Squamous Cell Carcinoma", "Stage IVA Epidermoid Carcinoma of Mouth", "Stage IVA Oral Cavity Squamous Cell Cancer", "Stage IVA Squamous Cell Carcinoma of Mouth", "Stage IVA Oral Cavity Epidermoid Carcinoma", "Stage IVA Epidermoid Carcinoma of the Mouth", "Stage IVA Epidermoid Carcinoma of Oral Cavity", "Stage IVA Oral Cavity Squamous Cell Carcinoma", "Stage IVA Squamous Cell Carcinoma of the Mouth", "Stage IVA Squamous Cell Carcinoma of Oral Cavity", "Stage IVA Epidermoid Carcinoma of the Oral Cavity", "Stage IVA Squamous Cell Carcinoma of the Oral Cavity", "Stage IVA Oral Cavity Squamous Cell Carcinoma AJCC v7", "Stage IVA Oral Cavity Squamous Cell Carcinoma AJCC v6", "Stage IVA Oral Cavity Squamous Cell Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Oral Cavity Squamous Cell Carcinoma AJCC v6 and v7", "shortest_name_length": 36}
{"curie": "UMLS:C4288037", "names": ["Vaginal Neuroendocrine Cancer", "Vaginal Neuroendocrine Carcinoma", "Vaginal High Grade Neuroendocrine Neoplasm", "Vaginal High Grade Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Neuroendocrine Carcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0003223", "names": ["hemangiopericytoma", "Meninges Hemangiopericytoma", "meninges hemangiopericytoma", "Meningeal hemangiopericytoma", "Meningeal Hemangiopericytoma", "meningeal hemangiopericytoma", "hemangiopericytoma of meninges", "Hemangiopericytoma of meninges", "Hemangiopericytoma of Meninges", "Haemangiopericytoma of meninges", "Meningeal Solitary Fibrous Tumor", "Hemangiopericytoma of the Meninges", "hemangiopericytoma of the meninges", "meningeal cluster spindle cell tumor", "meningeal cluster hemangiopericytoma", "Hemangiopericytoma of meninges (disorder)", "hemangiopericytoma of meninges (diagnosis)", "hemangiopericytoma of the central nervous system", "meningeal solitary fibrous tumor/hemangiopericytoma", "Meningeal Solitary Fibrous Tumor/Hemangiopericytoma", "central nervous system mass lesions meninges hemangiopericytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "meninges hemangiopericytoma", "shortest_name_length": 18}
{"curie": "MONDO:0043174", "names": ["Pfeiffer Tietze Welte syndrome", "sagittal craniostenosis, bilateral coloboma of the iris, craniofacial dysmorphy, asymmetrical split hand malformation, bilateral syndactyly of 2nd-4th"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pfeiffer Tietze Welte syndrome", "shortest_name_length": 30}
{"curie": "UMLS:C0152946", "names": ["Anthrax sepsis", "septic anthrax", "sepsis; anthrax", "anthrax; sepsis", "Septicemia anthrax", "Anthrax septicemia", "Anthrax septicaemia", "Septicaemia anthrax", "sepsis; Bacillus anthracis", "septic anthrax (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anthrax sepsis", "shortest_name_length": 14}
{"curie": "UMLS:C2981271", "names": ["Stage IVB Differentiated Thyroid Gland Cancer", "Stage IVB Differentiated Thyroid Gland Carcinoma", "Stage IVB Differentiated Thyroid Gland Carcinoma AJCC v7", "Stage IVB Thyroid Gland Papillary or Follicular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Differentiated Thyroid Gland Carcinoma AJCC v7", "shortest_name_length": 45}
{"curie": "UMLS:C4525072", "names": ["Refractory Histiocytic and Dendritic Cell Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Histiocytic and Dendritic Cell Neoplasm", "shortest_name_length": 50}
{"curie": "MONDO:0012045", "names": ["MYP5", "Myopia 5", "myopia 5, autosomal dominant", "MYOPIA 5, AUTOSOMAL DOMINANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopia 5, autosomal dominant", "shortest_name_length": 4}
{"curie": "MONDO:0017372", "names": ["Varicella embryopathy", "fetal varicella infection", "fetal effects of chickenpox", "congenital varicella syndrome", "Congenital varicella syndrome", "Congenital Varicella Syndrome", "fetal varicella zoster syndrome", "antenatal varicella virus infection", "Varicella virus antenatal infection", "fetal effects of varicella zoster virus", "Congenital varicella syndrome (disorder)", "mother-to-child transmission of varicella syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital varicella syndrome", "shortest_name_length": 21}
{"curie": "MONDO:0017211", "names": ["infectious panuveitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infectious panuveitis", "shortest_name_length": 21}
{"curie": "UMLS:C5446521", "names": ["Refractory Distal Bile Duct Adenocarcinoma", "Refractory Extrahepatic Cholangiocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Distal Bile Duct Adenocarcinoma", "shortest_name_length": 42}
{"curie": "UMLS:C3272837", "names": ["Colorectal Ganglioneuroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Ganglioneuroma", "shortest_name_length": 25}
{"curie": "MONDO:0019542", "names": ["acute failure liver", "Acute Liver Failure", "acute liver failure", "Acute liver failure", "Failure, Acute Liver", "Liver Failure, Acute", "acute failure hepatic", "hepatic failure acute", "acute hepatic failure", "failure hepatic acute", "HEPATIC FAILURE ACUTE", "Acute Hepatic Failure", "Acute hepatic failure", "Hepatic Failure, Acute", "Failure, Acute Hepatic", "liver acute failure alf", "Fulminant Liver Failure", "fulminant liver failure", "fulminate liver failure", "Liver Failure, Fulminant", "Fulminant Liver Failures", "Fulminant hepatic failure", "Fulminating Liver Failure", "ALF - Acute liver failure", "hepatic fulminant failure", "HEPATIC FAILURE FULMINANT", "Fulminant Hepatic Failure", "fulminant hepatic failure", "Fulminating Liver Failures", "Liver Failure, Fulminating", "Hepatic Failure, Fulminant", "Fulminant Hepatic Failures", "Fulminating Hepatic Failure", "Fulminating Hepatic Failures", "Hepatic Failure, Fulminating", "FHF - Fulminant hepatic failure", "Acute hepatic failure (disorder)", "acute hepatic failure (diagnosis)", "Fulminant hepatic failure (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute liver failure", "shortest_name_length": 19}
{"curie": "UMLS:C0267111", "names": ["Gastric dysplasia", "Gastric Dysplasia", "Stomach dysplasia", "gastric dysplasia", "stomach dysplasia", "dysplasia stomach", "Gastric dysplasia, NOS", "Gastric dysplasia (disorder)", "Gastric Intraepithelial Neoplasia", "Gastric Glandular Intraepithelial Neoplasia", "Gastric Glandular Intraepithelial Dysplasia", "Gastric Intraepithelial Neoplasia (Dysplasia)", "Stomach Intraepithelial Neoplasia (Dysplasia)", "Intraepithelial Neoplasia (Dysplasia) of Stomach", "Intraepithelial Neoplasia (Dysplasia) of the Stomach"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric dysplasia", "shortest_name_length": 17}
{"curie": "MONDO:0008985", "names": ["ciliary dyskinesia with transposition of ciliary microtubules", "CILIARY DYSKINESIA WITH TRANSPOSITION OF CILIARY MICROTUBULES", "Ciliary Dyskinesia With Transposition Of Ciliary Microtubules", "ciliary dyskinesia, due to transposition of ciliary microtubules"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ciliary dyskinesia with transposition of ciliary microtubules", "shortest_name_length": 61}
{"curie": "UMLS:C0234476", "names": ["True aphasia", "Aphasia, true", "Intellectual Aphasia", "Intellectual aphasia", "Aphasia, intellectual", "Aphasia, Intellectual", "Intellectual Aphasias", "Intellectual aphasia (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aphasia, Intellectual", "shortest_name_length": 12}
{"curie": "MONDO:0009526", "names": ["Fatco Syndrome", "FATCO SYNDROME", "FATCO syndrome", "Hecht-Scott syndrome", "limb deficiency-heart malformation syndrome", "Fibular aplasia-tibial campomelia-oligosyndactyly syndrome", "fibular aplasia-tibial campomelia-oligosyndactyly syndrome", "Fibular aplasia, tibial campomelia, oligo-syndactyly syndrome", "Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome", "FIBULAR APLASIA, TIBIAL CAMPOMELIA, AND OLIGOSYNDACTYLY SYNDROME", "fibular aplasia, tibial campomelia, and oligosyndactyly syndrome", "Fibular aplasia, tibial campomelia, oligo-syndactyly syndrome (disorder)", "terminal transverse defects of the limbs associated with congenital heart malformations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibular aplasia, tibial campomelia, and oligosyndactyly syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0018067", "names": ["Triploid", "Triploids", "Triploidy", "triploidy", "3n syndrome", "Triploidies", "69,XXY syndrome", "69,XXX syndrome", "Triploid Syndrome", "triploid syndrome", "triploidy syndrome", "Triploidy Syndrome", "Triploidy syndrome", "chromosome triploidy syndrome", "Triploidy syndrome (disorder)", "Triploidy (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "triploidy", "shortest_name_length": 8}
{"curie": "MONDO:0005176", "names": ["benign insulitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign insulitis", "shortest_name_length": 16}
{"curie": "UMLS:C4288306", "names": ["Recurrent Gastrointestinal Stromal Tumor", "Recurrent Gastrointestinal Stromal Tumor (GIST)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Gastrointestinal Stromal Tumor", "shortest_name_length": 40}
{"curie": "MONDO:0007195", "names": ["BIFID NOSE, AUTOSOMAL DOMINANT", "Bifid Nose, Autosomal Dominant", "bifid nose, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bifid nose, autosomal dominant", "shortest_name_length": 30}
{"curie": "MONDO:0007590", "names": ["facial asymmetry", "Friedreich's disease", "Facial hemihypertophy", "Facial Hemihypertrophy", "Hemifacial Hyperplasia", "HEMIFACIAL HYPERPLASIA", "facial hemihypertrophy", "Facial hemihyperplasia", "FACIAL HEMIHYPERTROPHY", "hemifacial hypertrophy", "HEMIFACIAL HYPERTROPHY", "Hemifacial enlargement", "hemifacial hyperplasia", "Hemifacial hypertrophy", "Hemifacial hyperplasia", "hypertrophy; hemifacial", "hemifacial; hypertrophy", "Overgrowth of half of face", "Enlargement of half of face", "Hypertrophy of half of face", "Increase in size of half of face", "Hemifacial hyperplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemifacial hypertrophy", "shortest_name_length": 16}
{"curie": "MONDO:0003826", "names": ["Mediastinal seminoma", "Mediastinal Seminoma", "mediastinal seminoma", "mediastinum seminoma", "seminoma of mediastinum", "Seminoma of mediastinum", "Seminoma of Mediastinum", "Seminoma of the Mediastinum", "seminoma of the mediastinum", "anterior mediastinal seminoma", "seminoma of mediastinum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mediastinum seminoma", "shortest_name_length": 20}
{"curie": "MONDO:0010159", "names": ["MMRCS", "BTPS1", "CMMRD", "BMMRD", "CMMRDS", "MMRCS1", "CMMR-D", "BTP1 SYNDROME", "BTP1 syndrome", "MMR DEFICIENCY", "MMR Deficiency", "MMR deficiency", "Turcot Syndrome", "Turcot syndrome", "CMMR-D syndrome", "turcot syndrome", "TURCOT SYNDROME", "syndrome turcots", "turcot's syndrome", "Turcot's syndrome", "CHILDHOOD CANCER SYNDROME", "glioma-polyposis syndrome", "childhood cancer syndrome", "mismatch repair deficiency", "MISMATCH REPAIR DEFICIENCY", "Turcot syndrome (disorder)", "Mismatch Repair Deficiency", "Constitutional MMR Deficiency", "brain tumor-polyposis syndrome", "mismatch repair cancer syndrome", "Mismatch repair cancer syndrome", "Mismatch Repair Cancer Syndrome", "brain tumor-polyposis syndrome 1", "BRAIN TUMOR-POLYPOSIS SYNDROME 1", "Brain Tumor-Polyposis Syndrome 1", "mismatch repair cancer syndrome 1", "MISMATCH REPAIR CANCER SYNDROME 1", "Biallelic Mismatch Repair Deficiency", "Constitutional Mismatch Repair Deficiency", "Biallelic Mismatch Repair Deficiency Syndrome", "CNS tumors with familial polyposis of the colon", "CNS tumors with Familial polyposis of the colon", "constitutional mismatch repair deficiency syndrome", "Constitutional mismatch repair deficiency syndrome", "CONSTITUTIONAL MISMATCH REPAIR DEFICIENCY SYNDROME", "Constitutional Mismatch Repair Deficiency Syndrome", "constitutional MIS-match repair deficiency syndrome", "Constitutional Mis-Match Repair Deficiency Syndrome", "CMMR-D (constitutional mismatch repair deficiency) syndrome", "Constitutional mismatch repair deficiency syndrome (disorder)", "malignant tumors of the central nervous system associated with familial polyposis of the colon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mismatch repair cancer syndrome 1", "shortest_name_length": 5}
{"curie": "UMLS:C4520855", "names": ["stage II endometrial cancer", "stage II cancer of the uterus", "Stage II Endometrial Cancer AJCC v6", "Stage II Uterine Corpus Cancer AJCC v6", "Stage II Cancer of Uterine Corpus AJCC v6", "Stage II Cancer of the Corpus Uteri AJCC v6", "Stage II Cancer of the Uterine Corpus AJCC v6", "Stage II Uterine (including Endometrial) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Uterine Corpus Cancer AJCC v6", "shortest_name_length": 27}
{"curie": "MONDO:0012545", "names": ["NLSDM", "neutral lipid storage myopathy", "Neutral lipid storage myopathy", "triglyceride deposit cardiomyovasculopathy", "Neutral lipid storage disease with myopathy", "NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY", "Neutral Lipid Storage Disease with Myopathy", "neutral lipid storage disease with myopathy", "neutral lipid storage disease without ichthyosis", "Neutral lipid storage disease without ichthyosis", "Neutral Lipid Storage Disease without Ichthyosis", "NEUTRAL LIPID STORAGE DISEASE WITHOUT ICHTHYOSIS", "Neutral lipid storage disease with myopathy (disorder)", "neutral lipid storage disease with myopathy without ichthyosis", "Neutral lipid storage disease with myopathy without ichthyosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neutral lipid storage myopathy", "shortest_name_length": 5}
{"curie": "MONDO:0008448", "names": ["Spheroid body myopathy", "spheroid body myopathy", "myopathy, spheroid body", "MYOPATHY, SPHEROID BODY", "Spheroid body myopathy (disorder)", "autosomal dominant spheroid body myopathy", "Autosomal dominant spheroid body myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spheroid body myopathy", "shortest_name_length": 22}
{"curie": "MONDO:0001927", "names": ["pi", "pulmonary regurg.", "Pulmonic regurgitation", "pulmonic insufficiency", "pulmonary incompetence", "pulmonic regurgitation", "Pulmonary incompetence", "Pulmonic insufficiency", "Pulmonary insufficiency", "PULMONARY INSUFFICIENCY", "PULMONARY REGURGITATION", "pulmonary insufficiency", "Pulmonary Insufficiency", "Pulmonary Regurgitation", "pulmonary regurgitation", "Pulmonary regurgitation", "pulmonary; regurgitation", "Regurgitation, Pulmonary", "pulmonary; insufficiency", "insufficiency; pulmonary", "regurgitation; pulmonary", "regurgitation, pulmonary", "Pulmonic incompetence NOS", "Pulmonic regurgitation NOS", "Pulmonic insufficiency NOS", "Pulmonic valve incompetence", "Pulmonic regurgitation, NOS", "pulmonic valve regurgitation", "Pulmonic valve insufficiency", "Pulmonary Valve Incompetence", "Pulmonic valve regurgitation", "Pulmonary valve incompetence", "PR - Pulmonary regurgitation", "pulmonary insufficiency (PI)", "pulmonary valve regurgitation", "Pulmonary Valve Insufficiency", "Pulmonary valve insufficiency", "PVR - Pulmonary regurgitation", "incompetency; pulmonary valve", "Incompetence, Pulmonary Valve", "Pulmonary Valve Regurgitation", "pulmonary valve insufficiency", "Valve Incompetence, Pulmonary", "Pulmonary valve regurgitation", "PULMONARY VALVE, INSUFFICIENCY", "PULMONARY VALVE, REGURGITATION", "Regurgitation, Pulmonary Valve", "Puolmonary valve insufficiency", "pulmonary valve; insufficiency", "Insufficiency, Pulmonary Valve", "Valve Insufficiency, Pulmonary", "pulmonary valve; regurgitation", "Valve Regurgitation, Pulmonary", "pulmonary; insufficiency, valve", "insufficiency; pulmonary, valve", "pulmonary valvular regurgitation", "Pulmonic valve incompetence, NOS", "pulmonary valvular insufficiency", "Pulmonary Valvular Insufficiency", "Pulmonary Valvular Regurgitation", "Pulmonic valve insufficiency, NOS", "Pulmonic valve regurgitation, NOS", "Pulmonary valve incompetence, NOS", "Pulmonary valve insufficiency, NOS", "pulmonary incompetence, non-rheumatic", "Pulmonary incompetence, non-rheumatic", "Pulmonary regurgitation, non-rheumatic", "Pulmonary insufficiency, non-rheumatic", "Pulmonic valve regurgitation (disorder)", "pulmonary valve regurgitation (diagnosis)", "pulmonary valve regurgitation nonrheumatic", "nonrheumatic pulmonary valve regurgitation", "Nonrheumatic pulmonary valve regurgitation", "Pulmonary valve regurgitation, nonrheumatic", "Pulmonary Valve Insufficiency/ Regurgitation", "Pulmonary incompetence, non-rheumatic (disorder)", "pulmonary insufficiency following trauma and surgery", "nonrheumatic pulmonary valve regurgitation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary valve insufficiency", "shortest_name_length": 2}
{"curie": "MONDO:0007227", "names": ["Sillence syndrome", "brachydactyly-symphalangism syndrome", "Brachydactyly-symphalangism syndrome", "BRACHYDACTYLY-DISTAL SYMPHALANGISM SYNDROME", "Brachydactyly-distal symphalangism syndrome", "brachydactyly-distal symphalangism syndrome", "Brachydactyly and distal symphalangism syndrome", "Brachydactyly and distal symphalangism syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sillence syndrome", "shortest_name_length": 17}
{"curie": "UMLS:C4727400", "names": ["Recurrent Pancreatic Cystadenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Pancreatic Cystadenocarcinoma", "shortest_name_length": 39}
{"curie": "UMLS:C0677695", "names": ["Stage II Diffuse Large Cell Lymphoma", "contiguous adult diffuse large cell lymphoma stage II", "Contiguous Adult Diffuse Large Cell Lymphoma Stage II", "contiguous stage II adult diffuse large cell lymphoma", "Stage II Contiguous Adult Diffuse Large Cell Lymphoma", "Contiguous Stage II Adult Diffuse Large Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Contiguous Adult Diffuse Large Cell Lymphoma", "shortest_name_length": 36}
{"curie": "MONDO:0011935", "names": ["RP30", "RP 30", "macular Degeneration", "retinitis pigmentosa 30", "RETINITIS PIGMENTOSA 30", "Retinitis Pigmentosa 30", "FSCN2 retinitis pigmentosa", "retinitis pigmentosa type 30", "retinitis pigmentosa caused by mutation in FSCN2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 30", "shortest_name_length": 4}
{"curie": "UMLS:C1334009", "names": ["ASIN-H", "High Grade Anal Canal Dysplasia", "High Grade Anal Canal Squamous Dysplasia", "High Grade Anal Canal Intraepithelial Neoplasia", "High Grade Anal Squamous Intraepithelial Neoplasia", "High Grade Anal Canal Squamous Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Anal Canal Intraepithelial Neoplasia", "shortest_name_length": 6}
{"curie": "UMLS:C0343500", "names": ["Bacillus; welchii", "Clostridium; welchii, gas gangrene", "gas gangrene Clostridium perfringens", "gas gangrene; Clostridium perfringens", "Clostridium; perfringens, gas gangrene", "Gas gangrene due to Clostridium welchii", "Gas gangrene caused by clostridium welchii", "gas gangrene due to Clostridium perfringens", "Gas gangrene due to Clostridium perfringens", "Gas gangrene caused by clostridium perfringens", "Gas gangrene infection due to Clostridium welchii", "gangrene; due to Clostridium perfringens or welchii", "Gas gangrene infection due to Clostridium perfringens", "gas gangrene due to Clostridium perfringens (diagnosis)", "Gas gangrene caused by clostridium perfringens (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gas gangrene caused by clostridium perfringens", "shortest_name_length": 17}
{"curie": "UMLS:C2046300", "names": ["Central Nervous System Histiocytic Sarcoma", "histiocytic sarcoma of central nervous system", "histiocytic sarcoma of central nervous system (diagnosis)", "central nervous system neoplasm malignant sarcoma histiocytic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "histiocytic sarcoma of central nervous system", "shortest_name_length": 42}
{"curie": "UMLS:C5401306", "names": ["SPG30", "Spastic Paraplegia 30"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spastic Paraplegia 30", "shortest_name_length": 5}
{"curie": "UMLS:C1096293", "names": ["macroangiopathy", "Macroangiopathy", "macroangiopathies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Macroangiopathy", "shortest_name_length": 15}
{"curie": "MONDO:0023180", "names": ["fragile X syndrome type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fragile X syndrome type 3", "shortest_name_length": 25}
{"curie": "MONDO:0010894", "names": ["MODY3", "MODY type 3", "MODY, Type 3", "MODY, TYPE 3", "MODY, type 3", "MODY, type III", "diabetes mellitus MODY type 3", "HNF1A-associated monogenic diabetes", "HNF1A-Associated Monogenic Diabetes", "maturity-onset diabetes of the young type 3", "type 3 maturity-onset diabetes of the young", "Maturity-onset diabetes of the young, type 3", "Maturity-Onset Diabetes of the Young, Type 3", "MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 3", "maturity-onset diabetes of the young, type 3", "maturity-onset diabetes of the young - type 3", "MODY hepatocyte nuclear factor-1-alpha related", "HNF1A maturity-onset diabetes of the young (disease)", "Maturity-onset diabetes of the young, type 3 (disorder)", "MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 3 (disorder)", "maturity-onset diabetes of the young - type 3 (diagnosis)", "Hepatocyte Nuclear Factor 1-Alpha-Associated Monogenic Diabetes", "hepatocyte nuclear Factor 1-Alpha-associated monogenic diabetes", "maturity-onset diabetes of the young (disease) caused by mutation in HNF1A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maturity-onset diabetes of the young type 3", "shortest_name_length": 5}
{"curie": "MONDO:0004516", "names": ["bulbomembranous urethral cancer", "bulbomembranous urethral malignant neoplasm", "Bulbomembranous Urethral Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bulbomembranous urethral cancer", "shortest_name_length": 31}
{"curie": "MONDO:0018486", "names": ["visual snow", "visual snow syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "visual snow syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0032597", "names": ["CMS24", "myasthenic syndrome, congenital, 24, presynaptic", "MYASTHENIC SYNDROME, CONGENITAL, 24, PRESYNAPTIC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myasthenic syndrome, congenital, 24, presynaptic", "shortest_name_length": 5}
{"curie": "UMLS:C4048264", "names": ["Nodular regenerative hyperplasia", "Nodular regenerative hyperplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nodular regenerative hyperplasia", "shortest_name_length": 32}
{"curie": "MONDO:0018100", "names": ["HOMG", "HOMG3", "hypomagnesemia", "Hypomagnesemia primary", "primary hypomagnesemia", "Primary hypomagnesemia", "HYPOMAGNESEMIA 3, RENAL", "Primary hypomagnesaemia", "Hypomagnesemia 3, Renal", "HYPOMAGNESEMIA, ISOLATED RENAL", "Hypomagnesemia, isolated renal", "primary familial hypomagnesemia", "Familial Primary Hypomagnesemia", "Primary familial hypomagnesemia", "familial primary hypomagnesemia", "Primary familial hypomagnesaemia", "Primary hypomagnesemia (disorder)", "Magnesium, defect in renal tubular transport of", "Familial hypomagnesemia with hypercalciuria and nephrocalcinosis", "Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis", "HYPOMAGNESEMIA, FAMILIAL, WITH HYPERCALCIURIA AND NEPHROCALCINOSIS", "Hypomagnesemia, familial, with hypercalciuria and nephrocalcinosis", "Hypomagnesemia, Primary, Due To Defect In Renal Tubular Transport Of Magnesium", "HYPOMAGNESEMIA, PRIMARY, DUE TO DEFECT IN RENAL TUBULAR TRANSPORT OF MAGNESIUM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial primary hypomagnesemia", "shortest_name_length": 4}
{"curie": "MONDO:0044795", "names": ["Epithelioid cell nevus", "epithelioid cell nevus", "Epithelioid Cell Nevus", "Epithelioid cell naevus", "[M] Epithelioid cell nevus", "[M] Epithelioid cell naevus", "Epithelioid cell nevus (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epithelioid cell nevus", "shortest_name_length": 22}
{"curie": "MONDO:0017822", "names": ["Mixed secreting pituitary adenoma", "mixed secreting pituitary adenoma", "Mixed functioning pituitary adenoma", "mixed functioning pituitary adenoma", "pituitary adenoma mixed functioning", "Mixed-functioning pituitary adenoma", "Mixed-functioning pituitary adenoma (disorder)", "Mixed-functioning pituitary adenoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed functioning pituitary adenoma", "shortest_name_length": 33}
{"curie": "MONDO:0020573", "names": ["genetic susceptibility", "genetic predisposition", "predisposition, genetic", "susceptibility, genetic", "genetic predispositions", "genetic susceptibilities", "predispositions, genetic", "susceptibilities, genetic", "inherited disease susceptibility", "Genetic Predisposition to Disease", "hereditary disease susceptibility", "hereditary predisposition to disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited disease susceptibility", "shortest_name_length": 22}
{"curie": "MONDO:0011784", "names": ["MYMY2", "Moyamoya disease 2", "Moyamoya Disease 2", "MOYAMOYA DISEASE 2", "Moyamoya disease type 2", "RNF213 Moyamoya disease", "moyamoya disease 2, susceptibility to", "Moyamoya disease caused by mutation in RNF213"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Moyamoya disease 2", "shortest_name_length": 5}
{"curie": "UMLS:C5555295", "names": ["Current_EBV_infection", "Current EBV Infection", "Current Epstein-Barr Virus Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Current EBV Infection", "shortest_name_length": 21}
{"curie": "UMLS:C0278848", "names": ["recurrent thymoma", "Recurrent Malignant Thymoma", "Thymoma Malignant Recurrent", "Thymoma malignant recurrent", "Malignant Thymoma, Recurrent", "recurrent thymoma and thymic carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thymoma malignant recurrent", "shortest_name_length": 17}
{"curie": "UMLS:C4527006", "names": ["Stage IB Retroperitoneal Sarcoma", "Stage IB Retroperitoneal Sarcoma AJCC v8", "Stage IB Soft Tissue Retroperitoneal Sarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Retroperitoneal Sarcoma AJCC v8", "shortest_name_length": 32}
{"curie": "UMLS:C1449626", "names": ["CADASILM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CADASILM", "shortest_name_length": 8}
{"curie": "MONDO:0007861", "names": ["cloverleaf skull", "Cloverleaf skull", "Kleeblattschadel", "KLEEBLATTSCHADEL", "CLOVERLEAF SKULL", "Kleeblattschaedel", "KLEEBLATTSCHAEDEL", "Trilobar skull shape", "Cloverleaf skull shape", "Trilobar cranium shape", "Cloverleaf-shaped skull", "Cloverleaf cranium shape", "cloverleaf skull syndrome", "Cloverleaf skull syndrome", "Kleeblattschaedel syndrome", "Kleeblattschadel deformity", "Clover leaf skull deformity", "isolated cloverleaf skull syndrome", "Kleeblattschaedel-deformity syndrome", "Kleeblattschaedel deformity syndrome", "Cloverleaf skull syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated cloverleaf skull syndrome", "shortest_name_length": 16}
{"curie": "UMLS:C0751553", "names": ["Childhood Tic Disorder", "Tic Disorder, Childhood", "Childhood Tic Disorders", "Tic Disorders, Childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Tic Disorders", "shortest_name_length": 22}
{"curie": "MONDO:0013331", "names": ["F5F8D2", "factor V and factor VIII, combined deficiency of", "factor V and factor VIII, combined deficiency of, 2", "FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 2", "factor 5 and Factor VIII, combined deficiency of, 2", "MCFD2 combined deficiency of factor V and factor VIII", "factor 5 and Factor VIII, combined deficiency of, type 2", "combined deficiency of factor V and factor VIII caused by mutation in MCFD2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "factor 5 and Factor VIII, combined deficiency of, 2", "shortest_name_length": 6}
{"curie": "UMLS:C5419511", "names": ["Atypical Vascular Lesion of Breast", "Atypical Vascular Proliferation of Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypical Vascular Lesion of Breast", "shortest_name_length": 34}
{"curie": "MONDO:0004083", "names": ["Bowen disease, clonal", "Clonal Bowen's disease", "Bowen's disease, clonal", "Borst-Jadassohn phenomenon", "Clonal intraepidermal carcinoma", "Bowen's disease, clonal (disorder)", "Intraepidermal epithelioma of Jadassohn", "Intraepidermal Epithelioma of Jadassohn", "intraepidermal epithelioma of Jadassohn", "Borst-Jadassohn intraepidermal carcinoma", "Borst-Jadassohn Intraepidermal Carcinoma", "Intraepidermal epithelioma of Borst-Jadassohn", "Intraepidermal epithelioma of Borsst-Jadassohn", "Intraepidermal epithelioma of Jadassohn (disorder)", "Intraepidermal epithelioma of Jadassohn (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borst-Jadassohn intraepidermal carcinoma", "shortest_name_length": 21}
{"curie": "MONDO:0100272", "names": ["PEX7 related peroxisome biogenesis disorder", "peroxisome biogenesis disorder due to PEX7 defect", "adult refsum disease due to PEX7 defect (formerly)", "rhizomelic chondrodysplasia punctata type 1 (formerly)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder due to PEX7 defect", "shortest_name_length": 43}
{"curie": "MONDO:0014589", "names": ["MODY13", "MODY type 13", "MODY, TYPE 13", "MODY, type 13", "maturity-onset diabetes of the young type 13", "maturity-onset diabetes of the young, type 13", "MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 13", "KCNJ11 maturity-onset diabetes of the young (disease)", "maturity-onset diabetes of the young (disease) caused by mutation in KCNJ11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maturity-onset diabetes of the young type 13", "shortest_name_length": 6}
{"curie": "UMLS:C0748726", "names": ["Allergic sinusitis", "SINUSITIS ALLERGIC", "Sinusitis;allergic", "allergic sinusitis", "sinusitis; allergic", "allergic; sinusitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Allergic sinusitis", "shortest_name_length": 18}
{"curie": "MONDO:0013192", "names": ["SPDA3", "ankylosing spondylitis 3", "SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 3", "spondyloarthropathy, susceptibility to, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloarthropathy, susceptibility to, 3", "shortest_name_length": 5}
{"curie": "MONDO:0019699", "names": ["slender bone dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "slender bone dysplasia", "shortest_name_length": 22}
{"curie": "MONDO:0015927", "names": ["Idiopathic eosinophilic pneumonia", "idiopathic eosinophilic pneumonia", "pneumonia idiopathic eosinophilic", "Idiopathic eosinophilic pneumonia (disorder)", "Idiopathic eosinophilic pneumonia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic eosinophilic pneumonia", "shortest_name_length": 33}
{"curie": "MONDO:0013923", "names": ["MCPH9", "primary autosomal recessive microcephaly 9", "microcephaly 9, primary, autosomal recessive", "MICROCEPHALY 9, PRIMARY, AUTOSOMAL RECESSIVE", "CEP152 autosomal recessive primary microcephaly", "autosomal recessive primary microcephaly caused by mutation in CEP152"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly 9, primary, autosomal recessive", "shortest_name_length": 5}
{"curie": "UMLS:C1880997", "names": ["Gonadotropin Secretion Abnormality"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gonadotropin Secretion Abnormality", "shortest_name_length": 34}
{"curie": "UMLS:C0271193", "names": ["peripheral visual field defect", "Peripheral visual field defect", "Peripheral Visual Field Defect", "Visual field defect, peripheral", "Peripheral visual field defect (finding)", "peripheral visual field defect (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peripheral visual field defect", "shortest_name_length": 30}
{"curie": "UMLS:C4527416", "names": ["Luminal B Prostate Cancer", "Luminal B Prostate Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Luminal B Prostate Carcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0018615", "names": ["Hemicrania continua", "Hemicrania Continua", "hemicrania continua", "Hemicrania continua (disorder)", "hemicrania continua (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemicrania continua", "shortest_name_length": 19}
{"curie": "MONDO:0000257", "names": ["Acute diarrhea", "acute diarrhea", "DIARRHEA ACUTE", "acute diarrhoea", "Diarrhoea;acute", "Acute diarrhoea", "diarrhea, acute", "acute diarrheal disease", "diarrheal disease, acute", "diarrhea (disease), acute", "Acute diarrhea (disorder)", "Acute diarrhea (diagnosis)", "intestinal disorder diarrheal acute"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute diarrhea", "shortest_name_length": 14}
{"curie": "MONDO:0015638", "names": ["benign partial epilepsy of infancy with complex partial seizures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign partial epilepsy of infancy with complex partial seizures", "shortest_name_length": 64}
{"curie": "MONDO:0010290", "names": ["MNG2", "goiter, multinodular 2", "GOITER, MULTINODULAR 2", "Goiter, Multinodular 2", "goiter, multinodular, 2, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "goiter, multinodular 2", "shortest_name_length": 4}
{"curie": "UMLS:C4727685", "names": ["Advanced Nasopharyngeal Squamous Cell Carcinoma", "Advanced Squamous Cell Carcinoma of the Nasopharynx", "Advanced Nasopharyngeal Throat Squamous Cell Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Nasopharyngeal Squamous Cell Carcinoma", "shortest_name_length": 47}
{"curie": "MONDO:0013751", "names": ["ADCL2", "autosomal dominant cutis laxa 2", "autosomal dominant cutis laxa-2", "CUTIS LAXA, AUTOSOMAL DOMINANT 2", "cutis laxa, autosomal dominant 2", "cutis laxa autosomal dominant adcl2", "FBLN5 autosomal dominant cutis laxa", "cutis laxa, autosomal dominant type 2", "autosomal dominant cutis laxa-2 (diagnosis)", "autosomal dominant cutis laxa caused by mutation in FBLN5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutis laxa, autosomal dominant 2", "shortest_name_length": 5}
{"curie": "UMLS:C0014571", "names": ["epiphysis slip", "epiphysiolysis", "EPIPHYSIOLYSIS", "Epiphysiolysis", "Epiphysiolyses", "Slipped Epiphysis", "slipped epiphysis", "Slipped Epiphyses", "slipped; epiphysis", "epiphysis; slipped", "Epiphyses, Slipped"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epiphyses, Slipped", "shortest_name_length": 14}
{"curie": "UMLS:C5447547", "names": ["Refractory Urethral Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Urethral Urothelial Carcinoma", "shortest_name_length": 40}
{"curie": "UMLS:C4288892", "names": ["Acute Undifferentiated Leukemia", "Infant Acute Undifferentiated Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infant Acute Undifferentiated Leukemia", "shortest_name_length": 31}
{"curie": "MONDO:0019914", "names": ["UPD(9)mat", "maternal uniparental disomy chromosome 9", "maternal uniparental disomy of chromosome 9", "Maternal uniparental disomy of chromosome 9", "maternal uniparental disomy of chromosome type 9", "Maternal uniparental disomy of chromosome 9 (disorder)", "Maternal uniparental disomy of chromosome 9 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maternal uniparental disomy of chromosome 9", "shortest_name_length": 9}
{"curie": "MONDO:0014015", "names": ["SPG56", "hereditary spastic paraplegia 56", "CYP2U1 hereditary spastic paraplegia", "hereditary spastic paraplegia type 56", "autosomal recessive spastic paraplegia 56", "SPASTIC PARAPLEGIA 56, AUTOSOMAL RECESSIVE", "spastic paraplegia 56, autosomal recessive", "autosomal recessive spastic paraplegia type 56", "Autosomal recessive spastic paraplegia type 56", "Autosomal recessive spastic paraplegia type 56 (disorder)", "hereditary spastic paraplegia caused by mutation in CYP2U1", "SPASTIC PARAPLEGIA 56, AUTOSOMAL RECESSIVE, WITH OR WITHOUT PSEUDOXANTHOMA ELASTICUM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 56", "shortest_name_length": 5}
{"curie": "MONDO:0018484", "names": ["SCD syndrome", "Minor's syndrome", "Minorbs syndrome", "superior canal syndrome", "canal dehiscence syndrome", "superior canal dehiscence", "third mobile window syndrome", "Superior canal dehiscence syndrome", "Superior Canal Dehiscence Syndrome", "semicircular canal dehiscence syndrome", "Superior Semicircular Canal Dehiscence", "superior semicircular canal dehiscence", "Superior semicircular canal dehiscence", "Dehiscence of the Superior Semicircular Canal", "SCCD - superior semicircular canal dehiscence", "Superior semicircular canal dehiscence (SCCD)", "Superior semicircular canal dehiscence syndrome", "superior semicircular canal dehiscence syndrome", "Superior Semicircular Canal Dehiscence Syndrome", "Superior semicircular canal dehiscence syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "semicircular canal dehiscence syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0019644", "names": ["unilateral renal dysplasia", "renal dysplasia, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal dysplasia, unilateral", "shortest_name_length": 26}
{"curie": "UMLS:C1709568", "names": ["Pleomorphic Hepatocellular Cancer", "Pleomorphic Hepatocellular Carcinoma", "Hepatocellular carcinoma, pleomorphic type", "Hepatocellular carcinoma, pleomorphic type (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pleomorphic Hepatocellular Carcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C4288540", "names": ["Ovarian Seromucinous Cystadenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Seromucinous Cystadenoma", "shortest_name_length": 32}
{"curie": "UMLS:C0854829", "names": ["T-Cell Lymphoma Stage II", "Stage II T-Cell Lymphoma", "Stage II T Cell Lymphoma", "T Cell Lymphoma Stage II", "T-cell lymphoma stage II", "T-cell lymphoma NOS stage II", "Stage II T-Cell Non-Hodgkin Lymphoma", "Stage II T-Cell Non-Hodgkin's Lymphoma", "Ann Arbor Stage II T-Cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-cell lymphoma stage II", "shortest_name_length": 24}
{"curie": "UMLS:C4040491", "names": ["Bronchopneumonia due to Haemophilus influenzae", "Bronchopneumonia caused by Haemophilus influenzae", "Bronchopneumonia caused by Haemophilus influenzae (disorder)", "Bronchopneumonia caused by Haemophilus influenzae (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bronchopneumonia due to Haemophilus influenzae", "shortest_name_length": 46}
{"curie": "MONDO:0007535", "names": ["EMPHYSEMA, HEREDITARY PULMONARY", "emphysema, hereditary pulmonary", "Emphysema, Hereditary Pulmonary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "emphysema, hereditary pulmonary", "shortest_name_length": 31}
{"curie": "MONDO:0002997", "names": ["anterior fossa meningioma", "Anterior Fossa Meningioma", "Meningioma of Anterior Fossa", "meningioma of anterior fossa", "meningioma of the anterior fossa", "Meningioma of the Anterior Fossa", "meningioma of the Anterior Fossa", "anterior cranial fossa meningioma", "Anterior Cranial Fossa Meningioma", "meningioma of anterior cranial fossa", "Meningioma of Anterior Cranial Fossa", "Meningioma of the Anterior Cranial Fossa", "meningioma of the anterior cranial fossa", "anterior cranial fossa meningioma (disease)", "meningioma (disease) of anterior cranial fossa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anterior cranial fossa meningioma", "shortest_name_length": 25}
{"curie": "MONDO:0002513", "names": ["benign renal tumor", "Benign Renal Tumor", "Benign renal tumor", "renal tumor, benign", "Renal Tumor, Benign", "Benign Kidney Tumor", "Benign renal tumour", "benign tumor kidney", "benign kidney tumor", "benign kidney tumors", "KIDNEY, BENIGN TUMOR", "benign renal neoplasm", "benign kidneys tumors", "Renal benign neoplasm", "Benign renal neoplasm", "Benign Renal Neoplasm", "Benign Tumor of Kidney", "Neoplasm benign;kidney", "kidney benign neoplasm", "Benign tumor of kidney", "Benign Kidney Neoplasm", "Renal neoplasms benign", "benign tumor of kidney", "Renal Neoplasm, Benign", "benign kidney neoplasm", "renal neoplasm, benign", "Benign tumour of kidney", "Kidney and Ureter Tumor", "renal and ureteral tumor", "Renal and Ureteral Tumor", "Benign renal neoplasm NOS", "Benign neoplasm of kidney", "benign neoplasm of kidney", "Benign Neoplasm of Kidney", "benign tumor of the kidney", "Kidney and Ureter Neoplasm", "Benign Tumor of the Kidney", "Renal and Ureteral Neoplasm", "Benign Neoplasm of the Kidney", "benign neoplasm of the kidney", "Benign neoplasm of kidney NOS", "Benign neoplasm of kidney, NOS", "Benign neoplasm of kidney (disorder)", "benign neoplasm of kidney (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kidney benign neoplasm", "shortest_name_length": 18}
{"curie": "MONDO:0019954", "names": ["PANET", "PanNET", "Pancreatic NET", "pancreatic NET", "islet cell tumor", "Islet Cell Tumor", "pancreatic endocrine tumor", "Islet cell tumors - pancreas", "islet cell tumors - pancreas", "Pancreatic Neuroendocrine Tumor", "pancreatic neuroendocrine tumor", "neuroendocrine tumor of pancreas", "Islet cell tumors of the pancreas", "islet cell tumors of the pancreas", "well-differentiated pancreatic NEN", "well-differentiated NEN of pancreas", "Well Differentiated Pancreatic Endocrine Tumor", "well differentiated pancreatic endocrine tumor", "Well Differentiated Pancreatic Endocrine Neoplasm", "well differentiated pancreatic endocrine neoplasm", "well-differentiated pancreatic neuroendocrine neoplasm", "well-differentiated neuroendocrine neoplasm of pancreas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic neuroendocrine tumor", "shortest_name_length": 5}
{"curie": "UMLS:C5447454", "names": ["IRF8 Deficiency", "IRF8, Dendritic cell immunodeficiency", "Interferon Regulatory Factor 8 Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Interferon Regulatory Factor 8 Deficiency", "shortest_name_length": 15}
{"curie": "UMLS:C1335700", "names": ["Recurrent Female Reproductive System Cancer", "Recurrent Female Reproductive System Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Female Reproductive System Carcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0002470", "names": ["TTD-P", "Tay syndrome", "IBIDS syndrome", "trichothiodystrophy", "photosensitive trichothiodystrophy", "sulfur-deficient brittle hair syndrome", "trichothiodystrophy with congenital ichtyosis", "trichothiodystrophy with congenital ichthyosis", "Ichtyosis, brittle hair, intellectual impairment, decreased fertility, and short stature"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "photosensitive trichothiodystrophy", "shortest_name_length": 5}
{"curie": "MONDO:0009718", "names": ["MYXEDEMA", "myxedema", "Myxedema", "MYXOEDEMA", "myxoedema", "Myxedemas", "Myxoedema", "Myxedema NOS", "Mucin in skin", "Myxedema, NOS", "Myxoedema, NOS", "Myxedema (disorder)", "myxedema (diagnosis)", "Hypothyroidism/myxedema", "Hypothyroidism/myxoedema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myxedema", "shortest_name_length": 8}
{"curie": "MONDO:0024339", "names": ["lymph node tumor", "tumor of lymph node", "Lymph Node Neoplasm", "lymph node neoplasm", "neoplasm of lymph node", "lymph node neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymph node neoplasm", "shortest_name_length": 16}
{"curie": "MONDO:0013872", "names": ["HPC2", "PROSTATE CANCER, HEREDITARY, 2", "prostate cancer, hereditary, 2", "ELAC2 familial prostate cancer", "prostate cancer, hereditary, type 2", "prostate cancer, hereditary, 2, susceptibility to", "familial prostate cancer caused by mutation in ELAC2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate cancer, hereditary, 2", "shortest_name_length": 4}
{"curie": "MONDO:0016971", "names": ["LGMD", "dystrophy; Erb", "Erb; dystrophy", "Limb-Girdle Syndrome", "limb-girdle syndrome", "Limb girdle dystrophy", "Erb's Muscular Dystrophy", "erb's muscular dystrophy", "Erb's muscular dystrophy", "Muscular dystrophy, Erb's", "limb-girdle syndrome (LGS)", "dystrophy; muscular, Erb type", "muscular; dystrophy, Erb type", "limb girdle muscular dystrophy", "muscular dystrophy limb-girdle", "myopathic limb-girdle syndrome", "Myopathic Limb-Girdle Syndrome", "limb-girdle muscular dystrophy", "Limb-Girdle Muscular Dystrophy", "Limb-girdle muscular dystrophy", "Limb Girdle Muscular Dystrophy", "Leyden-Mbius muscular dystrophy", "Muscular Dystrophy, Limb Girdle", "Muscular dystrophy, limb-girdle", "Muscular Dystrophy, Limb-Girdle", "limb-girdle muscular dystrophies", "Limb Girdle Muscular Dystrophies", "muscular; dystrophy, limb-girdle", "dystrophy; muscular, limb-girdle", "Limb-Girdle Muscular Dystrophies", "dystrophies girdle limb muscular", "Limb girdle muscular dystrophies", "Leyden-Mobius muscular dystrophy", "muscular dystrophy of limb-girdle", "Muscular Dystrophies, Limb-Girdle", "Muscular Dystrophies, Limb Girdle", "MUSCULAR DYSTROPHY, LIMB GIRDLE TYPE", "Erb's muscular dystrophy (diagnosis)", "limb-girdle muscular dystrophy (LGMD)", "progressive muscular dystrophy (Erb's)", "limb-girdle muscular weakness and atrophy", "Progressive muscular dystrophy, limb girdle", "Limb girdle muscular dystrophy, unspecified", "muscular dystrophy of limb-girdle (diagnosis)", "Muscular dystrophy with predominantly proximal limb girdle distribution", "Muscular dystrophy with predominantly proximal limb girdle distribution (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "limb-girdle muscular dystrophy", "shortest_name_length": 4}
{"curie": "MONDO:0016959", "names": ["partial trisomy of chromosome 8q", "partial duplication of chromosome 8q", "partial trisomy of the long arm of chromosome 8", "partial duplication of the long arm of chromosome 8", "partial duplication of the long arm of chromosome type 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of the long arm of chromosome 8", "shortest_name_length": 32}
{"curie": "UMLS:C0280483", "names": ["Anaplastic Astrocytoma", "Grade 3 Adult Astrocytoma", "Adult Grade 3 Astrocytoma", "Adult Grade III Astrocytoma", "Grade III Adult Astrocytoma", "Adult Anaplastic Astrocytoma", "adult anaplastic astrocytoma", "anaplastic astrocytoma, adult", "astrocytoma, adult anaplastic", "Grade 3 Adult Astrocytic Tumor", "Anaplastic Astrocytoma of Adult", "Grade III Adult Astrocytic Tumor", "Grade 3 Adult Astrocytic Neoplasm", "Adult Undifferentiated Astrocytoma", "Anaplastic Astrocytoma of the Adult", "Grade III Adult Astrocytic Neoplasm", "Undifferentiated Astrocytoma of Adult", "Undifferentiated Astrocytoma of the Adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Anaplastic Astrocytoma", "shortest_name_length": 22}
{"curie": "UMLS:C0279948", "names": ["adult NHL stage", "Adult NonHodgkins Lymphoma Stage", "stage, adult non-Hodgkin lymphoma", "Adult Non-Hodgkins Lymphoma Stage", "Adult NonHodgkin's Lymphoma Stage", "Stage Adult Non-Hodgkin's Lymphoma", "adult non-Hodgkin's lymphoma stage", "Adult Non-Hodgkin's Lymphoma Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Non-Hodgkin's Lymphoma Stage", "shortest_name_length": 15}
{"curie": "MONDO:0030899", "names": ["OCA8", "Oculocutaneous albinism type 8", "oculocutaneous albinism type 8", "oculocutaneous albinism, type 8", "OCULOCUTANEOUS ALBINISM, TYPE VIII", "oculocutaneous albinism, type VIII", "ALBINISM, OCULOCUTANEOUS, TYPE VIII"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculocutaneous albinism type 8", "shortest_name_length": 4}
{"curie": "MONDO:0044723", "names": ["MGA8", "MGCA8", "3-methylglutaconic aciduria type 8", "3-Methylglutaconic aciduria, type 8", "3-methylglutaconic aciduria type VIII", "3-methylglutaconic aciduria, type VIII", "3-METHYLGLUTACONIC ACIDURIA, TYPE VIII", "3-@METHYLGLUTACONIC ACIDURIA, TYPE VIII", "3-methylglutaconic aciduria type VIII, MGCA8", "3-methylglutaconic aciduria, type VIII; MGCA8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "3-methylglutaconic aciduria type 8", "shortest_name_length": 4}
{"curie": "MONDO:0018717", "names": ["mixed cystic lymphangioma", "mixed cystic lymphatic malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed cystic lymphatic malformation", "shortest_name_length": 25}
{"curie": "MONDO:0000987", "names": ["Strawberry gallbladder", "strawberry gallbladder", "strawberry; gallbladder", "gallbladder; strawberry", "GALLBLADDER, STRAWBERRY", "Gallbladder cholesterolosis", "Cholesterolosis of gallbladder", "cholesterolosis of gallbladder", "Cholesterolosis of gallbladder (disorder)", "cholesterolosis of gallbladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholesterolosis of gallbladder", "shortest_name_length": 22}
{"curie": "MONDO:0020746", "names": ["CPSKF1B", "CPSFS1B", "Autosomal recessive multiple pterygium syndrome", "CONTRACTURES, PTERYGIA, AND VARIABLE SKELETAL FUSIONS SYNDROME 1B", "contractures, pterygia, and variable skeletal fusions syndrome 1B", "CONTRACTURES, PTERYGIA, AND SPONDYLOCARPOTARSAL FUSION SYNDROME 1B", "contractures, pterygia, and spondylocarpotarsal fusion syndrome 1B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "contractures, pterygia, and variable skeletal fusions syndrome 1B", "shortest_name_length": 7}
{"curie": "MONDO:0020297", "names": ["Noonan like syndrome", "Noonan syndrome and Noonan-related syndrome", "Noonan-like-multiple giant cell lesion syndrome", "Noonan Syndrome With Pigmented Villonodular Synovitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Noonan syndrome and Noonan-related syndrome", "shortest_name_length": 20}
{"curie": "MONDO:0018656", "names": ["TACH syndrome", "tremor-ataxia-central hypomyelination syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tremor-ataxia-central hypomyelination syndrome", "shortest_name_length": 13}
{"curie": "UMLS:C4521734", "names": ["Stage IIIB Esophageal Squamous Cell Cancer", "Postneoadjuvant Therapy Stage IIIB Esophageal Squamous Cell Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postneoadjuvant Therapy Stage IIIB Esophageal Squamous Cell Carcinoma AJCC v8", "shortest_name_length": 42}
{"curie": "MONDO:0022413", "names": ["Albright-like syndrome", "Albright like syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Albright-like syndrome", "shortest_name_length": 22}
{"curie": "MONDO:0009253", "names": ["FRNS", "fryn syndrome", "Fryns syndrome", "Fryns Syndrome", "FRYNS SYNDROME", "fryns syndrome", "Moerman Van den berghe Fryns syndrome", "Moerman Van den Berghe Fryns syndrome", "Diaphragmatic hernia, abnormal face and distal limb anomalies", "DIAPHRAGMATIC HERNIA, ABNORMAL FACE, AND DISTAL LIMB ANOMALIES", "Diaphragmatic hernia, abnormal face, and distal limb anomalies", "diaphragmatic hernia, abnormal face, and distal limb anomalies", "Diaphragmatic hernia-abnormal face-distal limb anomalies syndrome", "diaphragmatic hernia-abnormal face-distal limb anomalies syndrome", "Diaphragmatic hernia, abnormal face and distal limb anomalies (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fryns syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0333980", "names": ["Focal nodular hyperplasia", "Focal Nodular Hyperplasia", "nodular focal hyperplasia", "focal nodular hyperplasia", "focal hyperplasia nodular", "nodular hyperplasia focal", "Hyperplasia, Focal Nodular", "Focal Nodular Hyperplasias", "Hyperplasias, Focal Nodular", "Focal nodular hyperplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Focal Nodular Hyperplasia", "shortest_name_length": 25}
{"curie": "UMLS:C5237030", "names": ["Recurrent Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Neuroendocrine Carcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0005256", "names": ["moderate heart failure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "moderate heart failure", "shortest_name_length": 22}
{"curie": "MONDO:0013425", "names": ["RP20", "RP 20", "retinitis pigmentosa 20", "RETINITIS PIGMENTOSA 20", "Retinitis Pigmentosa 20", "RPE65 retinitis pigmentosa", "retinitis pigmentosa type 20", "retinitis pigmentosa caused by mutation in RPE65"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 20", "shortest_name_length": 4}
{"curie": "MONDO:0049222", "names": ["MRX107", "XLID107", "X-linked mental retardation 107", "MENTAL RETARDATION, X-LINKED 107", "mental retardation, X-linked 107", "intellectual disability, X-linked 107", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 107", "intellectual developmental disorder, X-linked 107", "non-syndromic X-linked intellectual disability 107"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 107", "shortest_name_length": 6}
{"curie": "UMLS:C1112470", "names": ["Infusion site inflammation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infusion site inflammation", "shortest_name_length": 26}
{"curie": "UMLS:C1336104", "names": ["Stage 0is Renal Pelvis and Ureter Cancer", "Stage 0is Renal Pelvis and Ureter Cancer AJCC v7", "Stage 0is Renal Pelvis and Ureter Urothelial Carcinoma", "Stage 0is Renal Pelvis and Ureter Urothelial Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0is Renal Pelvis and Ureter Cancer AJCC v7", "shortest_name_length": 40}
{"curie": "MONDO:0024572", "names": ["Immunosuppression disorders", "Immunodepression-Related Disorder", "immunodeficiency-related disorder", "Immunodepression-related disorder", "Immunodeficiency-Related Disorder", "Immunosuppression-related disorder", "Immunosuppression-Related Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency-related disorder", "shortest_name_length": 27}
{"curie": "MONDO:0045022", "names": ["organic acid metabolism disorder", "disorder of organic acid metabolism", "organic acid metabolic process disease", "disorder of organic acid metabolic process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of organic acid metabolism", "shortest_name_length": 32}
{"curie": "UMLS:C1332241", "names": ["Ameloblastic Carcinoma Ex Ameloblastoma", "Ameloblastic Carcinoma-Secondary Type (Dedifferentiated)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ameloblastic Carcinoma-Secondary Type (Dedifferentiated)", "shortest_name_length": 39}
{"curie": "MONDO:0012638", "names": ["MOBA", "MCOPS10", "MOBA syndrome", "syndromic microphthalmia 10", "microphthalmia syndromic 10", "MICROPHTHALMIA, SYNDROMIC 10", "microphthalmia, syndromic 10", "Microphthalmia, Syndromic 10", "Microphthalmia and Brain Atrophy", "microphthalmia and brain atrophy", "Syndromic microphthalmia type 10", "syndromic microphthalmia type 10", "MICROPHTHALMIA AND BRAIN ATROPHY", "Microphthalmia-brain atrophy syndrome", "microphthalmia-brain atrophy syndrome", "Microphthalmia with brain atrophy syndrome", "Microphthalmia with brain atrophy syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microphthalmia-brain atrophy syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0005139", "names": ["Severe obesity", "obesity morbid", "severe obesity", "morbid obesity", "Morbid Obesity", "Morbid obesity", "obesity severe", "Severe Obesity", "OBESITY MORBID", "Obesity, Severe", "Obesity, severe", "obesity; morbid", "morbid; obesity", "OBESITY, SEVERE", "OBESITY EXTREME", "Obesity, Morbid", "Severe Obesities", "extreme; obesity", "Morbid Obesities", "obesity; extreme", "Obesity, extreme", "Obesities, Severe", "Obesities, Morbid", "Severe obesity (disorder)", "Morbid obesity (disorder)", "morbid obesity (diagnosis)", "severe obesity (diagnosis)", "obesity morbid due to excess calories", "obesity morbid due to excess calories (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "morbid obesity", "shortest_name_length": 14}
{"curie": "MONDO:0032679", "names": ["COXPD37", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 37", "combined oxidative phosphorylation deficiency 37"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation deficiency 37", "shortest_name_length": 7}
{"curie": "MONDO:0012312", "names": ["SQT1", "SQTS", "Short QT Syndrome 1", "SHORT QT SYNDROME 1", "short QT syndrome 1", "KCNH2 short QT syndrome", "short QT syndrome type 1", "short QT syndrome caused by mutation in KCNH2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short QT syndrome type 1", "shortest_name_length": 4}
{"curie": "MONDO:0005910", "names": ["phagocytic dysfunction", "Phagocyte Bactericidal Dysfunction", "phagocyte bactericidal dysfunction", "Phagocyte Bactericidal Dysfunctions", "Bactericidal Dysfunction, Phagocyte", "Dysfunction, Phagocyte Bactericidal", "Bactericidal Dysfunctions, Phagocyte", "Dysfunctions, Phagocyte Bactericidal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phagocyte bactericidal dysfunction", "shortest_name_length": 22}
{"curie": "MONDO:0009826", "names": ["Alpha-2-globulin polymorphism Pa", "PA polymorphism of alpha-2-globulin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PA polymorphism of alpha-2-globulin", "shortest_name_length": 32}
{"curie": "MONDO:0001716", "names": ["corneal argyrosis", "argentous deposits", "argyrosis of cornea", "Argyrosis of cornea", "Argentous corneal deposit", "corneal deposits argentous", "argentous corneal deposits", "Argentous corneal deposits", "argentous deposits of cornea", "Argentous corneal deposit (disorder)", "Argentous corneal deposits (diagnosis)", "argentous deposits were observed in the cornea", "argentous deposits of cornea (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal argyrosis", "shortest_name_length": 17}
{"curie": "EFO:1001482", "names": ["cardiotoxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiotoxicity", "shortest_name_length": 14}
{"curie": "MONDO:0020249", "names": ["hereditary optic neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary optic neuropathy", "shortest_name_length": 27}
{"curie": "UMLS:C0269596", "names": ["bleed pregnancy", "bleeds pregnancy", "Antenatal bleeding", "bleeding pregnancy", "pregnancy bleeding", "hemorrhage pregnancy", "HEMORRHAGE PREGNANCY", "pregnancy hemorrhage", "Hemorrhage pregnancy", "Haemorrhage pregnancy", "in pregnancy bleeding", "pregnancy; hemorrhage", "hemorrhage; pregnancy", "bleeding in pregnancy", "Hemorrhage of pregnancy", "Hemorrhage of Pregnancy", "HEMORRHAGE OF PREGNANCY", "Bleeding (in);pregnancy", "hemorrhage of pregnancy", "HEMORRHAGE IN PREGNANCY", "Hemorrhage in pregnancy", "hemorrhage in pregnancy", "Haemorrhage in pregnancy", "Haemorrhage of pregnancy", "HAEMORRHAGE IN PREGNANCY", "bleeding during pregnancy", "Hemorrhage of pregnancy NOS", "Hemorrhage of pregnancy, NOS", "Haemorrhage of pregnancy, NOS", "preg complications: hemorrhagic", "Hemorrhagic complication of pregnancy", "Hemorrhagic Complication of Pregnancy", "Haemorrhagic complication of pregnancy", "HEMORRHAGIC COMPLICATIONS OF PREGNANCY", "Hemorrhagic complications of pregnancy", "Haemorrhagic complications of pregnancy", "Hemorrhagic complication of pregnancy (disorder)", "Hemorrhagic complication of pregnancy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemorrhagic complication of pregnancy", "shortest_name_length": 15}
{"curie": "UMLS:C1512435", "names": ["High Grade Prostatic Intraepithelial Neoplasia, Foamy Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Prostatic Intraepithelial Neoplasia, Foamy Variant", "shortest_name_length": 61}
{"curie": "MONDO:0006241", "names": ["Liver granuloma", "LIVER GRANULOMA", "granuloma liver", "liver granuloma", "Liver Granuloma", "granulomas liver", "granuloma; liver", "liver; granuloma", "granuloma hepatic", "Hepatic Granuloma", "hepatic granuloma", "Hepatic granuloma", "granulomas hepatic", "Hepatic granuloma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatic granuloma", "shortest_name_length": 15}
{"curie": "UMLS:C0340911", "names": ["AV Fistula Aneurysm", "Arteriovenous fistula aneurysm", "Arteriovenous Fistula Aneurysm", "Arteriovenous fistula aneurysm (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arteriovenous fistula aneurysm", "shortest_name_length": 19}
{"curie": "MONDO:0019585", "names": ["scleromyxedema without monoclonal gammopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scleromyxedema without monoclonal gammopathy", "shortest_name_length": 44}
{"curie": "MONDO:0012887", "names": ["IBD23", "INFLAMMATORY BOWEL DISEASE 23", "inflammatory bowel disease 23", "Inflammatory Bowel Disease 23", "inflammatory bowel disease type 23"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory bowel disease 23", "shortest_name_length": 5}
{"curie": "MONDO:0013794", "names": ["THCYT3", "thrombocytosis 3", "THROMBOCYTOSIS 3", "thrombocythemia 3", "THROMBOCYTHEMIA 3", "thrombocythemia type 3", "JAK2 familial thrombocytosis", "familial thrombocytosis caused by mutation in JAK2", "thrombocythemia 3, autosomal dominant, somatic mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombocythemia 3", "shortest_name_length": 6}
{"curie": "MONDO:0100436", "names": ["CCL", "CTRCT2", "Coppock-like cataract", "CATARACT, COPPOCK-LIKE", "Cataract, Coppock-like", "cataract, Coppock-like", "Cataract, Coppock-Like", "cataract 2 multiple types", "CATARACT 2, MULTIPLE TYPES", "cataract 2, multiple types", "Cataract, Embryonic Nuclear", "Pulverulent nuclear cataract", "Central pulverulent cataract", "Nuclear pulverulent cataract", "cataracta pulverulenta centralis", "cataract 2 multiple types with or without microcornea", "CATARACT 2, MULTIPLE TYPES, WITH OR WITHOUT MICROCORNEA", "cataract 2, multiple types, with or without microcornea"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 2, multiple types", "shortest_name_length": 3}
{"curie": "UMLS:C4683157", "names": ["Progressive Disease in Neuroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Progressive Disease in Neuroblastoma", "shortest_name_length": 36}
{"curie": "MONDO:0003274", "names": ["thorax cancer", "Thoracic tumor", "thoracic tumor", "cancer thoracic", "thorax neoplasm", "thoracic cancer", "tumor of thorax", "Malignant Thoracic Tumor", "malignant thoracic tumor", "thorax/respiratory cancer", "Malignant tumor of thorax", "Malignant Tumor of Thorax", "malignant tumor of thorax", "respiratory/thorax cancer", "Malignant tumour of thorax", "malignant thoracic neoplasm", "Malignant Thoracic Neoplasm", "Malignant neoplasm of thorax", "malignant neoplasm of thorax", "Malignant Neoplasm of Thorax", "malignant tumor of the thorax", "Malignant Tumor of the Thorax", "Thoracic malignant neoplasm NOS", "Malignant Neoplasm of the Thorax", "malignant neoplasm of the thorax", "thoracic segment of trunk cancer", "cancer of thoracic segment of trunk", "Malignant neoplasm of thorax (disorder)", "malignant neoplasm of the thorax (diagnosis)", "malignant thoracic segment of trunk neoplasm", "malignant tumor of ill-defined site of thorax", "malignant neoplasm of thoracic segment of trunk", "malignant neoplasm of ill-defined site of thorax"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thoracic cancer", "shortest_name_length": 13}
{"curie": "UMLS:C4053792", "names": ["Pauci-Immune Glomerulonephritis - Renal Limited", "Pauci-immune Glomerulonephritis - Renal Limited"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pauci-Immune Glomerulonephritis - Renal Limited", "shortest_name_length": 47}
{"curie": "UMLS:C4683417", "names": ["Stage I Differentiated Thyroid Gland Cancer Under 55 Years", "Stage I Differentiated Thyroid Gland Carcinoma Under 55 Years AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Differentiated Thyroid Gland Carcinoma Under 55 Years AJCC v8", "shortest_name_length": 58}
{"curie": "UMLS:C4329969", "names": ["Factor VIII Inactivation", "Factor VIII Inhibitor Present"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Factor VIII Inactivation", "shortest_name_length": 24}
{"curie": "MONDO:0009731", "names": ["Braun-Bayer syndrome", "nephrosis deafness urinary tract digital malformation", "Nephrosis deafness urinary tract digital malformation", "nephrosis-deafness-urinary tract-digital malformations syndrome", "NEPHROSIS WITH DEAFNESS AND URINARY TRACT AND DIGITAL MALFORMATIONS", "Nephrosis with deafness and urinary tract and digital malformations", "nephrosis with deafness and urinary tract and digital malformations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrosis-deafness-urinary tract-digital malformations syndrome", "shortest_name_length": 20}
{"curie": "MONDO:0020683", "names": ["Acute disease", "acute disease", "disease acute", "Acute Disease", "acute disorder", "Acute diseases", "Disease, Acute", "Acute Diseases", "disease, acute", "acute diseases", "Diseases, Acute", "acute disorders", "Acute disease, NOS", "acute disease/disorder", "Acute disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute disease", "shortest_name_length": 13}
{"curie": "MONDO:0012320", "names": ["MHP3", "FHM3", "familial hemiplegic migraine 3", "MIGRAINE, FAMILIAL HEMIPLEGIC, 3", "Migraine, Familial Hemiplegic, 3", "migraine, familial hemiplegic, 3", "migraine, familial hemiplegic, type 3", "SCN1A familial or sporadic hemiplegic migraine", "familial or sporadic hemiplegic migraine caused by mutation in SCN1A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "migraine, familial hemiplegic, 3", "shortest_name_length": 4}
{"curie": "UMLS:C3897928", "names": ["Phrenic Nerve Palsy Related to Birth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Phrenic Nerve Palsy Related to Birth", "shortest_name_length": 36}
{"curie": "MONDO:0700010", "names": ["chromosome 3 disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 3 disorder", "shortest_name_length": 21}
{"curie": "MONDO:0021507", "names": ["benign brainstem tumor", "Benign Brainstem Tumor", "Benign Brainstem Tumors", "benign brainstem tumors", "benign brain stem tumor", "Benign Brain Stem Tumor", "benign tumor of brainstem", "Benign Brainstem Neoplasm", "brainstem benign neoplasm", "Benign Tumor of Brainstem", "benign brainstem neoplasm", "Benign Tumor of Brain Stem", "Benign Tumors of Brainstem", "Benign Brainstem Neoplasms", "benign brainstem neoplasms", "benign brain stem neoplasm", "Benign Brain Stem Neoplasm", "benign tumor of brain stem", "benign tumors of brainstem", "Benign Brain Stem Neoplasms", "benign brain stem neoplasms", "Benign Neoplasm of Brainstem", "benign neoplasm of brainstem", "benign neoplasm of brain stem", "Benign neoplasm of brain stem", "Benign Neoplasm of Brain Stem", "benign tumor of the brainstem", "benign neoplasms of brainstem", "Benign Tumor of the Brainstem", "Benign Neoplasms of Brainstem", "benign tumor of the brain stem", "Benign Tumor of the Brain Stem", "benign tumors of the brainstem", "Benign Tumors of the Brainstem", "benign neoplasm of the brainstem", "Benign Neoplasm of the Brainstem", "Benign Neoplasms of the Brainstem", "benign neoplasms of the brainstem", "Benign Neoplasm of the Brain Stem", "benign neoplasm of the brain stem", "Benign neoplasm of brain stem (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of brain stem", "shortest_name_length": 22}
{"curie": "MONDO:0010022", "names": ["senile plaque formation", "SENILE PLAQUE FORMATION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "senile plaque formation", "shortest_name_length": 23}
{"curie": "MONDO:0013664", "names": ["TDD", "SRXY8", "46XY sex reversal 8", "46,XY SEX REVERSAL 8", "46,XY sex reversal 8", "46,XY sex reversal type 8", "Steroid 17,20-lyase deficiency", "46XY sex reversal 8, modifier of", "Defective synthesis of 17-20 desmolase", "17 alpha-Hydroxyprogesterone aldolase deficiency", "17 alpha-Hydroxyprogesterone aldolase deficiency (disorder)", "MALE PSEUDOHERMAPHRODITISM: DEFICIENCY OF TESTICULAR 17,20-DESMOLASE", "Male pseudohermaphroditism due to testicular 17,20-desmolase deficiency", "male pseudohermaphroditism due to deficiency of testicular 17,20-desmolase", "MALE PSEUDOHERMAPHRODITISM DUE TO DEFICIENCY OF TESTICULAR 17,20-DESMOLASE", "Male Pseudohermaphroditism due to Deficiency of Testicular 17,20-Desmolase", "46,XY disorder of sex development due to testicular 17,20-desmolase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XY disorder of sex development due to testicular 17,20-desmolase deficiency", "shortest_name_length": 3}
{"curie": "UMLS:C5418567", "names": ["Locally Advanced Endometrial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Endometrial Carcinoma", "shortest_name_length": 38}
{"curie": "MONDO:0008914", "names": ["Sanchez Cascos cardioauditory syndrome", "cardioauditory syndrome of Sanchez Cascos", "CARDIOAUDITORY SYNDROME OF SANCHEZ CASCOS", "Cardioauditory syndrome of Sanchez Cascos"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardioauditory syndrome of Sanchez Cascos", "shortest_name_length": 38}
{"curie": "MONDO:0001352", "names": ["round ligament of uterus cancer", "malignant round ligament neoplasm", "round ligament malignant neoplasm", "malignant tumor of round ligament", "cancer of round ligament of uterus", "Malignant neoplasm of round ligament", "malignant neoplasm of round ligament", "malignant round ligament of uterus neoplasm", "Malignant neoplasm of round ligament of uterus", "malignant neoplasm of round ligament of uterus", "Malignant neoplasm of round ligament (disorder)", "malignant neoplasm of round ligament (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "round ligament malignant neoplasm", "shortest_name_length": 31}
{"curie": "MONDO:0016575", "names": ["PCD", "ICS", "Kartagener", "siewert syndrome", "Siewert syndrome", "Siewert Syndrome", "KARTAGENER TRIAD", "SIEWERT SYNDROME", "kartagener triad", "Kartagener Triad", "Kartageners Triad", "Kartagener; triad", "triad; Kartagener", "Syndrome, Siewert", "Kartagener's Triad", "kartagener's triad", "ciliary dyskinesia", "Ciliary dyskinesia", "Ciliary Dyskinesia", "Kartagener syndrome", "Dyskinesia, Ciliary", "Kartagener Syndrome", "kartagener syndrome", "Ciliary Dyskinesias", "KARTAGENER SYNDROME", "Dysmotility Syndrome", "Kartageners Syndrome", "Syndrome, Kartagener", "kartageners syndrome", "Kartageners syndrome", "kartagener's syndrome", "Kartagener's Syndrome", "Kartagener's syndrome", "kartagener's syndromes", "Syndrome, Kartagener's", "IMMOTILE CILIA SYNDROME", "cilia immotile syndrome", "Immotile Cilia Syndrome", "immotile cilia syndrome", "Ciliary Motility Defect", "Immotile cilia syndrome", "Immotile Cilia Syndromes", "immotile cilia syndromes", "Dysmotile cilia syndrome", "Polynesian Bronchiectasis", "Polynesian bronchiectasis", "Polynesian Bronchiectases", "POLYNESIAN BRONCHIECTASIS", "ciliary motility disorder", "immotile ciliary syndrome", "Ciliary Motility Disorder", "Primary Ciliary Dyskinesia", "ciliary dyskinesia primary", "Disorder, Ciliary Motility", "Ciliary Motility Disorders", "primary ciliary dyskinesia", "Bronchiectasis, Polynesian", "Primary ciliary dyskinesia", "Dyskinesia, Primary Ciliary", "Ciliary Dyskinesia, Primary", "ICS - Immotile cilia syndrome", "Kartagener syndrome (disorder)", "PCD - Primary ciliary dyskinesia", "Kartagener's syndrome (diagnosis)", "Immotile cilia syndrome (disorder)", "primary ciliary dyskinesia (diagnosis)", "Immotile cilia syndrome, Kartagener type", "Dextrocardia bronchiectasis and sinusitis", "Primary ciliary dyskinesia, Kartagener type", "Dextrocardia, Bronchiectasis, and Sinusitis", "DEXTROCARDIA, BRONCHIECTASIS, AND SINUSITIS", "Primary ciliary dyskinesia and situs inversus", "Dextrocardia-bronchiectasis-sinusitis syndrome", "DEXTROCARDIA-BRONCHIECTASIS-SINUSITIS SYNDROME", "Lack of coordinated beating of respiratory cilia", "SINUSITIS-BRONCHIECTASIS-SITUS INVERSUS SYNDROME", "Bronchiectasis-chronic sinusitis and dextrocardia syndrome", "Bronchiectasis, chronic sinusitis and dextrocardia syndrome", "Bronchiectasis, chronic sinusitis AND dextrocardia syndrome", "bronchiectasis, chronic sinusitis and dextrocardia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia", "shortest_name_length": 3}
{"curie": "UMLS:C0863127", "names": ["Chemotherapy-Related Leukemia", "Leukemia secondary to oncology chemotherapy", "Leukaemia secondary to oncology chemotherapy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chemotherapy-Related Leukemia", "shortest_name_length": 29}
{"curie": "MONDO:0013811", "names": ["COXPD9", "combined oxidative phosphorylation deficiency 9", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 9", "combined oxidative phosphorylation defect type 9", "Combined oxidative phosphorylation defect type 9", "MRPL3 combined oxidative phosphorylation deficiency", "combined oxidative phosphorylation deficiency type 9", "COXPD9 - combined oxidative phosphorylation defect type 9", "Combined oxidative phosphorylation defect type 9 (disorder)", "combined oxidative phosphorylation defect type 9 (diagnosis)", "combined oxidative phosphorylation deficiency caused by mutation in MRPL3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation defect type 9", "shortest_name_length": 6}
{"curie": "MONDO:0011620", "names": ["Metaphyseal dysplasia Braun Tinschert type", "METAPHYSEAL DYSPLASIA, BRAUN-TINSCHERT TYPE", "Metaphyseal dysplasia, Braun-Tinschert type", "Metaphyseal Dysplasia, Braun-Tinschert Type", "metaphyseal dysplasia, Braun-Tinschert type", "Metaphyseal dysplasia Braun Tinschert type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metaphyseal dysplasia, Braun-Tinschert type", "shortest_name_length": 42}
{"curie": "MONDO:0060662", "names": ["DBAL", "Diamond-Blackfan anemia-like", "DIAMOND-BLACKFAN ANEMIA-LIKE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diamond-Blackfan anemia-like", "shortest_name_length": 4}
{"curie": "MONDO:0016892", "names": ["Monosomy 10p", "monosomy 10p", "10p- syndrome", "del(10p) syndrome", "partial monosomy 10p+", "deletion 10p syndrome", "10p deletion syndrome", "chromosome 10p monosomy", "Chromosome 10, 10p- Partial", "Chromosome 10, monosomy 10p", "chromosome 10p deletion syndrome", "Partial monosomy of chromosome 10p", "partial deletion of chromosome 10p", "partial monosomy of chromosome 10p", "Partial deletion of chromosome 10p", "Chromosome 10, Partial Deletion (short arm)", "Partial monosomy of the short arm of chromosome 10", "Partial deletion of the short arm of chromosome 10", "partial monosomy of the short arm of chromosome 10", "partial deletion of the short arm of chromosome 10", "partial deletion of the short arm of chromosome type 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of the short arm of chromosome 10", "shortest_name_length": 12}
{"curie": "UMLS:C0015411", "names": ["eye find", "Eye Findings", "eye findings", "Eye Manifestation", "eye manifestation", "Manifestation, Eye", "Eye Manifestations", "Manifestations, Eye", "Ocular manifestations of general diseases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eye Manifestations", "shortest_name_length": 8}
{"curie": "MONDO:0019153", "names": ["Goossens Devriendt syndrome", "Goossens-Devriendt syndrome", "brain malformation-congenital heart disease-postaxial polydactyly syndrome", "Brain malformation-congenital heart disease-postaxial polydactyly syndrome", "Brain malformation, congenital heart disease, postaxial polydactyly syndrome", "Brain malformation, congenital heart disease, postaxial polydactyly syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brain malformation-congenital heart disease-postaxial polydactyly syndrome", "shortest_name_length": 27}
{"curie": "MONDO:0033260", "names": ["DFNA73", "DEAFNESS, AUTOSOMAL DOMINANT 73", "deafness, autosomal dominant 73", "hearing loss, autosomal dominant 73", "autosomal dominant nonsyndromic deafness 73"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal dominant 73", "shortest_name_length": 6}
{"curie": "MONDO:0015252", "names": ["BD syndrome", "intellectual disability - athetosis - microphthalmia", "intellectual disability-athetosis-microphthalmia syndrome", "severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0009522", "names": ["Berlin syndrome", "Berlin syndrome (disorder)", "ectodermal dysplasia, Berlin type", "Ectodermal dysplasia, Berlin type", "Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis", "LEUKOMELANODERMA, infantilism, mental retardation, hypodontia, hypotrichosis", "LEUKOMELANODERMA, INFANTILISM, MENTAL RETARDATION, HYPODONTIA, HYPOTRICHOSIS", "LEUKOMELANODERMA, infantilism, intellectual disability, hypodontia, hypotrichosis", "Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome", "shortest_name_length": 15}
{"curie": "UMLS:C0221473", "names": ["emotional; blindness", "hysterical blindness", "Hysterical blindness", "blindness; emotional", "BLINDNESS HYSTERICAL", "Blindness hysterical", "Hysterical Blindness", "hysterical; blindness", "blindness; hysterical", "Blindness, Hysterical", "Dissociative blindness", "Dissociative blindness (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Blindness, Hysterical", "shortest_name_length": 20}
{"curie": "UMLS:C5418962", "names": ["Visceral Angiosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Visceral Angiosarcoma", "shortest_name_length": 21}
{"curie": "UMLS:C1112632", "names": ["Cross reactive drug hypersensitivity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cross reactive drug hypersensitivity", "shortest_name_length": 36}
{"curie": "UMLS:C4524723", "names": ["Gastroesophageal Junction Adenocarcinoma by AJCC v8 pTNM Stage", "Gastroesophageal Junction Adenocarcinoma by AJCC v8 Pathologic Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastroesophageal Junction Adenocarcinoma by AJCC v8 Pathologic Stage", "shortest_name_length": 62}
{"curie": "UMLS:C5555190", "names": ["Refractory Primary Peritoneal Transitional Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Primary Peritoneal Transitional Cell Carcinoma", "shortest_name_length": 57}
{"curie": "UMLS:C5556346", "names": ["Recurrent Tectal Glioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Tectal Glioma", "shortest_name_length": 23}
{"curie": "UMLS:C0271638", "names": ["NIDDM in obese", "diabetes mellitus type 2 in obese", "Type 2 diabetes mellitus in obese", "Diabetes mellitus type 2 in obese", "Diabetes mellitus type 2 in obese (disorder)", "diabetes mellitus type 2 in obese (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Type 2 diabetes mellitus in obese", "shortest_name_length": 14}
{"curie": "MONDO:0009203", "names": ["FFDD3", "FFDD type 2", "FFDD type III", "Setleis syndrome", "SETLEIS SYNDROME", "FACIAL ECTODERMAL DYSPLASIA", "facial ectodermal dysplasia", "focal facial dermal dysplasia II", "bitemporal forceps Marks syndrome", "bitemporal forceps marks syndrome", "BITEMPORAL FORCEPS MARKS SYNDROME", "bitemporal aplasia cutis congenita", "focal facial dermal dysplasia type 2", "focal Facial dermal dysplasia, type II", "familial focal facial dermal dysplasia", "Focal facial dermal dysplasia type III", "focal facial dermal dysplasia type III", "Congenital ectodermal dysplasia of face", "congenital ectodermal dysplasia of face", "focal facial dermal dysplasia II (FFDD II)", "FOCAL FACIAL DERMAL DYSPLASIA 3, SETLEIS TYPE", "focal facial dermal dysplasia 3, Setleis type", "Focal facial dermal dysplasia 3, Setleis type", "FOCAL FACIAL DERMAL DYSPLASIA, TYPE II, FORMERLY", "focal Facial dermal dysplasia, type II, formerly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal facial dermal dysplasia type III", "shortest_name_length": 5}
{"curie": "MONDO:0013419", "names": ["C1SD", "C1s Deficiency", "C1s DEFICIENCY", "C1s deficiency", "COMPLEMENT COMPONENT C1s DEFICIENCY", "Complement Component C1s Deficiency", "complement component C1s deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complement component C1s deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0013773", "names": ["BSVD2", "POREN2", "porencephaly 2", "POREN2, FORMERLY", "GOULD SYNDROME 2", "COL4A2 porencephaly", "porencephaly type 2", "PORENCEPHALY 2, FORMERLY", "BRAIN SMALL VESSEL DISEASE 2", "brain small vessel disease 2", "porencephaly caused by mutation in COL4A2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "porencephaly 2", "shortest_name_length": 5}
{"curie": "MONDO:0018853", "names": ["Greither disease", "progressive diffuse PPK", "transgrediens et progrediens PPK", "progressive diffuse palmoplantar keratoderma", "keratosis extremitatum hereditaria progrediens", "keratosis palmoplantaris transgrediens et progrediens", "transgrediens et progrediens palmoplantar keratoderma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transgrediens et progrediens palmoplantar keratoderma", "shortest_name_length": 16}
{"curie": "MONDO:0026762", "names": ["WRWFFR", "Wieacker-Wolff syndrome, female-restricted", "WIEACKER-WOLFF SYNDROME, FEMALE-RESTRICTED", "Wieacker-Wolff syndrome, female-restricted, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wieacker-Wolff syndrome, female-restricted", "shortest_name_length": 6}
{"curie": "MONDO:0012316", "names": ["MJDS", "CDA and CRMO", "Majeed Syndrome", "Majeed syndrome", "MAJEED syndrome", "MAJEED SYNDROME", "Majeed's syndrome", "Dyserythropoietic anemia, and neutrophilic dermatosis", "dyserythropoietic anemia, and neutrophilic dermatosis", "Chronic recurrent multifocal osteomyelitis, congenital", "chronic recurrent multifocal osteomyelitis, congenital", "Congenital dyserythropoietic anemia and chronic recurrent multifocal osteomyelitis", "congenital dyserythropoietic anemia and chronic recurrent multifocal osteomyelitis", "Chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anemia and neutrophilic dermatosis", "Chronic Recurrent Multifocal Osteomyelitis, Congenital Dyserythropoietic Anemia, and Neutrophilic Dermatosis", "Chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anaemia and neutrophilic dermatosis", "chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic Anemia, and neutrophilic dermatosis", "CHRONIC RECURRENT MULTIFOCAL OSTEOMYELITIS, CONGENITAL DYSERYTHROPOIETIC ANEMIA, AND NEUTROPHILIC DERMATOSIS", "Chronic recurrent multifocal osteomyelitis-congenital dyserythropoietic anemia-neutrophilic dermatosis syndrome", "chronic recurrent multifocal osteomyelitis-congenital dyserythropoietic anemia-neutrophilic dermatosis syndrome", "Chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anemia and neutrophilic dermatosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Majeed syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0333899", "names": ["Severe Koilocytotic Atypia", "Severe koilocytotic atypia", "Severe koilocytotic atypia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Severe koilocytotic atypia", "shortest_name_length": 26}
{"curie": "UMLS:C1698259", "names": ["HCV coinfection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HCV coinfection", "shortest_name_length": 15}
{"curie": "MONDO:0011612", "names": ["NKH", "NKA", "TNH", "GCE", "Glycine Encephalopathy", "glycine encephalopathy", "GLYCINE ENCEPHALOPATHY", "Glycine encephalopathy", "GLYCINE encephalopathy", "Encephalopathy, Glycine", "Glycine Encephalopathies", "Encephalopathies, Glycine", "Nonketotic hyperglycinemia", "hyperglycinemia nonketotic", "nonketotic hyperglycinemia", "Nonketotic Hyperglycinemia", "Non-ketotic hyperglycinemia", "Nonketotic hyperglycinaemia", "Glycine synthase deficiency", "Nonketotic Hyperglycinemias", "Non ketotic hyperglycinemia", "Hyperglycinemia, Nonketotic", "non-ketotic hyperglycinemia", "Non-Ketotic Hyperglycinemia", "Non ketotic Hyperglycinemia", "Non-ketotic Hyperglycinemia", "HYPERGLYCINEMIA, NONKETOTIC", "hyperglycinemia, Nonketotic", "Non-ketotic Hyperglycinemias", "non-ketotic hyperglycinaemia", "Non-ketotic hyperglycinaemia", "Non ketotic hyperglycinaemia", "Hyperglycinemias, Nonketotic", "Hyperglycinemia, Non-ketotic", "Hyperglycinemias, Non-ketotic", "Hyperglycinemia, nonketotic form", "NKH - Non-ketotic hyperglycinemia", "Transient neonatal hyperglycinemia", "NKH - Non-ketotic hyperglycinaemia", "Transient neonatal hyperglycinaemia", "HYPERGLYCINEMIA, TRANSIENT NEONATAL", "Hyperglycinemia, Transient Neonatal", "hyperglycinemia, transient neonatal", "hyperglycinemia nonketotic (diagnosis)", "Non-ketotic hyperglycinemia (disorder)", "Disorder of glycine cleavage enzyme complex", "Transient neonatal hyperglycinemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycine encephalopathy", "shortest_name_length": 3}
{"curie": "UMLS:C0043253", "names": ["Blunt trauma", "Blunt injury", "TRAUMA BLUNT", "Blunt Injury", "trauma blunt", "blunt trauma", "blunt injury", "injury blunt", "Injury, Blunt", "Blunt Injuries", "Injuries, Blunt", "Blunt injury, NOS", "Blunt force injury", "blunt force injury", "Nonpenetrating Wound", "Nonpenetrating Injury", "Nonpenetrating Wounds", "Wound, Nonpenetrating", "Injury, Nonpenetrating", "Wounds, Nonpenetrating", "Nonpenetrating Injuries", "Blunt force injury, NOS", "Blunt injury (disorder)", "blunt injury (diagnosis)", "Injuries, Nonpenetrating", "Blunt injury (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nonpenetrating Wounds", "shortest_name_length": 12}
{"curie": "MONDO:0004587", "names": ["Oguchi", "Oguchi disease", "Oguchi syndrome", "Oguchi's disease", "Hereditary night blindness", "hereditary night blindness", "congenital night blindness", "night blindness congenital", "Congenital night blindness", "Night blindness, congenital", "Oguchi's disease (disorder)", "Oguchi's disease (diagnosis)", "congenital night blindness (diagnosis)", "Stationary night blindness, Oguchi type", "Night blindness, congenital, Oguchi type", "Congenital stationary night blindness, Oguchi type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary night blindness", "shortest_name_length": 6}
{"curie": "MONDO:0002481", "names": ["ovary NET", "ovary neuroendocrine tumor", "neuroendocrine tumor of ovary", "ovary neuroendocrine neoplasm", "neuroendocrine tumor of Ovary", "Ovarian Neuroendocrine Neoplasm", "ovarian neuroendocrine neoplasm", "Neuroendocrine Neoplasm of Ovary", "neuroendocrine neoplasm of ovary", "Neuroendocrine Neoplasm of the Ovary", "neuroendocrine neoplasm of the ovary", "ovary neuroendocrine tumor, well differentiated, low or intermediate grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian neuroendocrine neoplasm", "shortest_name_length": 9}
{"curie": "UMLS:C0263628", "names": ["calcinosis tumoral", "tumoral calcinosis", "Tumoral Calcinosis", "Tumoral calcinosis", "Tumoral Calcinoses", "Calcinosis, tumoral", "Calcinoses, Tumoral", "Calcinosis, Tumoral", "Tumoural calcinosis", "Tumoral lipocalcinosis", "Teutschlander's disease", "Lipocalcinogranulomatosis", "Familial tumoral calcinosis", "Tumoral calcinosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tumoral calcinosis", "shortest_name_length": 18}
{"curie": "MONDO:0044013", "names": ["Puerperal Disorder", "disease; puerperal", "puerperal disorder", "postpartum disorder", "disorder, puerperal", "Puerperal Disorders", "Puerperal disorders", "puerperium; disease", "Postpartum disorder", "Disorder, Puerperal", "Disorders, Puerperal", "disorders, puerperal", "puerperium; disorder", "Disorder of puerperium", "disorder of puerperium", "Postpartum disorder NOS", "Disorder of the puerperium", "disease (or disorder); puerperal", "Disorder of puerperium (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "puerperal disorder", "shortest_name_length": 18}
{"curie": "MONDO:0021641", "names": ["Bunyavirus infection", "Bunyavirus infections", "Bunyaviridae Infection", "infections, Bunyavirus", "Bunyaviridae infection", "Bunyaviridae Infections", "Infections, Bunyaviridae", "infections, Bunyaviridae", "Disease due to Bunyavirus", "disease due to Bunyavirus", "DISEASES DUE TO BUNYAVIRUS", "infection due to bunyavirus", "Disease due to Bunyaviridae", "disease due to Bunyaviridae", "disease caused by Bunyavirus", "Disease caused by Bunyavirus", "DISEASES DUE TO BUNYAVIRIDAE", "Disease due to Bunyavirus, NOS", "Disease caused by Bunyaviridae", "disease caused by Bunyaviridae", "Bunyaviridae infectious disease", "Bunyaviridae disease or disorder", "Bunyaviridae caused disease or disorder", "infection due to bunyavirus (diagnosis)", "Disease caused by Bunyaviridae (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bunyaviridae infectious disease", "shortest_name_length": 20}
{"curie": "MONDO:0009764", "names": ["COMA", "Cogan's syndrome", "Oculomotor apraxia", "oculomotor; apraxia", "apraxia; oculomotor", "Ocular motor apraxia", "Oculomotor dyspraxia", "Ocular Motor Apraxia", "OCULAR MOTOR APRAXIA", "ocular motor apraxia", "Cogan syndrome type 2", "Cogan's syndrome type 2", "Cogan's syndrome, type 2", "oculomotor apraxia; Cogan", "Cogan; oculomotor apraxia", "Cogan's oculomotor apraxia", "Oculomotor apraxia (disorder)", "Ocular motor apraxia syndrome", "Congenital oculomotor apraxia", "congenital oculomotor apraxia", "Congenital Oculomotor Apraxia", "oculomotor apraxia Cogan type", "Oculomotor Apraxia, Cogan Type", "oculomotor apraxia, Cogan type", "OCULOMOTOR APRAXIA, COGAN TYPE", "Oculomotor apraxia, Cogan type", "Apraxia, oculomotor, Cogan type", "Oculomotor apraxia - Cogan type", "Ocular motor apraxia Cogan type", "Ocular motor apraxia, Cogan type", "ocular motor apraxia, Cogan type", "saccade initiation failure congenital", "Congenital saccade initiation failure", "Saccade initiation failure, congenital", "SACCADE INITIATION FAILURE, CONGENITAL", "saccade initiation failure, congenital", "oculomotor apraxia, congenital, Cogan-type", "Ocular motor apraxia Cogan type (disorder)", "Defective or absent horizontal voluntary eye movements"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ocular motor apraxia, Cogan type", "shortest_name_length": 4}
{"curie": "UMLS:C1334181", "names": ["Inflammatory Malignant Fibrous Histiocytoma NCI Grade 2", "Inflammatory Malignant Fibrous Histiocytoma NCI Grade II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Inflammatory Malignant Fibrous Histiocytoma NCI Grade 2", "shortest_name_length": 55}
{"curie": "UMLS:C0281871", "names": ["Stage IVA Hodgkin Lymphoma", "Hodgkin's Disease Stage IVa", "Stage IVA Hodgkin's Disease", "Hodgkin's Disease Stage IVA", "Hodgkin's Lymphoma Stage IVA", "Stage IVA Hodgkin's Lymphoma", "Ann Arbor Stage IVA Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage IVA Hodgkin Lymphoma", "shortest_name_length": 26}
{"curie": "UMLS:C1336062", "names": ["Splenic Manifestation of CLL", "Splenic Manifestation of Chronic Lymphocytic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Splenic Manifestation of Chronic Lymphocytic Leukemia", "shortest_name_length": 28}
{"curie": "MONDO:0014333", "names": ["Pmgr", "PMGR", "BPPR", "polymicrogyria, bilateral perisylvian", "polymicrogyria, bilateral perisylvian, autosomal recessive", "POLYMICROGYRIA, BILATERAL PERISYLVIAN, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polymicrogyria, bilateral perisylvian, autosomal recessive", "shortest_name_length": 4}
{"curie": "UMLS:C4552185", "names": ["Post procedural fever"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post procedural fever", "shortest_name_length": 21}
{"curie": "MONDO:0017989", "names": ["JET", "His bundle tachycardia", "junctional tachycardia", "Junctional tachycardia", "JUNCTIONAL TACHYCARDIA", "junctional ectopic tachycardia", "Ectopic Junctional Tachycardia", "Junctional Ectopic Tachycardia", "Junctional ectopic tachycardia", "Ectopic Junctional Tachycardias", "Tachycardia, Junctional Ectopic", "Ectopic Tachycardia, Junctional", "Tachycardia, Ectopic Junctional", "Junctional Tachycardia, Ectopic", "Junctional Ectopic Tachycardias", "Tachycardias, Ectopic Junctional", "Ectopic Tachycardias, Junctional", "Tachycardias, Junctional Ectopic", "Junctional Tachycardias, Ectopic", "His bundle tachycardia (disorder)", "His bundle tachycardia (diagnosis)", "Junctional ectopic tachycardia (disorder)", "junctional ectopic tachycardia (diagnosis)", "His Bundle (junctional ectopic) tachycardia", "His bundle (junctional ectopic) tachycardia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "His bundle tachycardia", "shortest_name_length": 3}
{"curie": "MONDO:0004773", "names": ["iridocyclitis", "IRIDOCYCLITIS", "Iridocyclitis", "Iridocyclitides", "Iridocyclitis, NOS", "iridocyclitis primary", "primary iridocyclitis", "Primary iridocyclitis", "Heterochromic Cyclitis", "Cyclitis, Heterochromic", "iridocyclitis (disease)", "Heterochromic Cyclitides", "Iridocyclitis (disorder)", "iridocyclitis (diagnosis)", "Cyclitides, Heterochromic", "Unspecified iridocyclitis", "iridocyclitis was observed", "Iridocyclitis, unspecified", "Certain types of iridocyclitis", "iridocyclitis (physical finding)", "Primary iridocyclitis (disorder)", "primary iridocyclitis (diagnosis)", "Inflammation of iris and ciliary body"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "iridocyclitis", "shortest_name_length": 13}
{"curie": "UMLS:C1096267", "names": ["Injection site discomfort"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site discomfort", "shortest_name_length": 25}
{"curie": "MONDO:0200000", "names": ["Broad Ligament Adenosarcoma", "uterine ligament adenosarcoma", "adenosarcoma of uterine ligament"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine ligament adenosarcoma", "shortest_name_length": 27}
{"curie": "MONDO:0008210", "names": ["MDPT1", "patterned macular dystrophy 1", "macular dystrophy, patterned, 1", "MACULAR DYSTROPHY, PATTERNED, 1", "PRPH2 patterned macular dystrophy", "patterned macular dystrophy type 1", "macular dystrophy, patterned, type 1", "macular dystrophy, butterfly-shaped pigmentary", "macular dystrophy, butterfly-Shaped pigmentary", "butterfly-shaped pigment dystrophy of the fovea", "butterfly-shaped pigmentary maculary dystrophy 1", "patterned dystrophy of retinal pigment epithelium", "butterfly dystrophy of retinal pigment epithelium", "patterned macular dystrophy caused by mutation in PRPH2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "patterned macular dystrophy 1", "shortest_name_length": 5}
{"curie": "MONDO:0000874", "names": ["T lymphoblastic lymphoma", "T Lymphoblastic Lymphoma", "childhood T lymphoblastic lymphoma", "Childhood T-Lymphoblastic Lymphoma", "Childhood T lymphoblastic lymphoma", "Childhood T Lymphoblastic Lymphoma", "T-cell childhood lymphoblastic lymphoma", "childhood precursor T-lymphoblastic lymphoma", "Childhood Precursor T-Lymphoblastic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-cell childhood lymphoblastic lymphoma", "shortest_name_length": 24}
{"curie": "MONDO:0011946", "names": ["DIAPHANOSPONDYLODYSOSTOSIS", "Diaphanospondylodysostosis", "diaphanospondylodysostosis", "Diaphanospondylodysostosis (disorder)", "Vertebral Ossification, Defect in, with Nephrogenic Rests", "vertebral ossification, defect in, with nephrogenic rests", "VERTEBRAL OSSIFICATION, DEFECT IN, WITH NEPHROGENIC RESTS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diaphanospondylodysostosis", "shortest_name_length": 26}
{"curie": "UMLS:C4527325", "names": ["Refractory Gray Zone Lymphoma", "Refractory B-Cell Lymphoma, Unclassifiable, with Features Intermediate between Diffuse Large B-Cell Lymphoma and Classic Hodgkin Lymphoma", "Refractory B-Cell Lymphoma, Unclassifiable, with Features Intermediate between Diffuse Large B-Cell Lymphoma and Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory B-Cell Lymphoma, Unclassifiable, with Features Intermediate between Diffuse Large B-Cell Lymphoma and Classic Hodgkin Lymphoma", "shortest_name_length": 29}
{"curie": "MONDO:0014394", "names": ["DBA13", "DIAMOND-BLACKFAN ANEMIA 13", "Diamond-Blackfan anemia 13", "RPS29 Diamond-Blackfan anemia", "Diamond-Blackfan Anemia type 13", "RPS29-related Diamond-Blackfan anemia", "Diamond-Blackfan anemia caused by mutation in RPS29"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diamond-Blackfan anemia 13", "shortest_name_length": 5}
{"curie": "UMLS:C0919728", "names": ["Unwanted awareness during anesthesia", "Unwanted awareness during anaesthesia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unwanted awareness during anesthesia", "shortest_name_length": 36}
{"curie": "MONDO:0013488", "names": ["APLDC3", "lipodystrophy, partial, acquired, associated with C3 nephritic Factor", "LIPODYSTROPHY, PARTIAL, ACQUIRED, ASSOCIATED WITH C3 NEPHRITIC FACTOR", "lipodystrophy, partial, acquired, with low complement component c3, with or without glomerulonephritis", "lipodystrophy, partial, acquired, with LOW complement component C3, with or without glomerulonephritis", "LIPODYSTROPHY, PARTIAL, ACQUIRED, WITH LOW COMPLEMENT COMPONENT C3, WITH OR WITHOUT GLOMERULONEPHRITIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lipodystrophy, partial, acquired, with low complement component c3, with or without glomerulonephritis", "shortest_name_length": 6}
{"curie": "MONDO:0007698", "names": ["HFG", "HFU", "HFGS", "HFG Syndrome", "HFU syndrome", "HFU Syndrome", "HFG syndrome", "HAND-FOOT-UTERUS SYNDROME", "Hand-Foot-Uterus Syndrome", "hand foot uterus syndrome", "Hand foot uterus syndrome", "hand-foot-uterus syndrome", "Hand-foot-uterus syndrome", "Hand-foot-genital syndrome", "HAND-FOOT-GENITAL SYNDROME", "Hand-Foot-Genital Syndrome", "hand foot genital syndrome", "Hand foot genital syndrome", "hand-foot-genital syndrome", "Hand-foot-genital syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hand-foot-genital syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0004340", "names": ["Mixed ductal-endocrine carcinoma", "mixed ductal-endocrine carcinoma", "Mixed Ductal-Endocrine Carcinoma", "mixed ductal-endocrine carcinoma of pancreas", "Mixed Ductal-Endocrine Carcinoma of the Pancreas", "Pancreatic Mixed Ductal-Neuroendocrine Carcinoma", "mixed ductal-endocrine carcinoma of the pancreas", "Mixed ductal-neuroendocrine carcinoma of pancreas", "mixed ductal-neuroendocrine carcinoma of the pancreas", "Mixed Ductal-Neuroendocrine Carcinoma of the Pancreas", "Mixed ductal-endocrine carcinoma (morphologic abnormality)", "Mixed ductal-neuroendocrine carcinoma of pancreas (disorder)", "Mixed ductal-neuroendocrine carcinoma of pancreas (diagnosis)", "pancreatic neoplasm malignant carcinoma mixed ductal-neuroendocrine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed ductal-endocrine carcinoma of pancreas", "shortest_name_length": 32}
{"curie": "MONDO:0002270", "names": ["Viral Gastritis", "viral gastritis", "Gastritis viral", "Viral gastritis", "Gastritis viral NOS", "Viral gastritis (disorder)", "viral gastritis (diagnosis)", "Viruses gastritis (disease)", "Viruses caused gastritis (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "viral gastritis", "shortest_name_length": 15}
{"curie": "UMLS:C1710175", "names": ["Lung Squamous Cell Carcinoma, Papillary Variant", "Squamous Cell Lung Carcinoma, Papillary Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Squamous Cell Carcinoma, Papillary Variant", "shortest_name_length": 47}
{"curie": "MONDO:0019916", "names": ["UPD(16)mat", "maternal uniparental disomy of chromosome 16", "maternal uniparental disomy of chromosome type 16"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maternal uniparental disomy of chromosome 16", "shortest_name_length": 10}
{"curie": "UMLS:C0348801", "names": ["Group B", "streptococcal group B pneumonia", "group b streptococcal pneumonia", "Group B streptococcal pneumonia", "group B streptococcal pneumonia", "streptoccocal; pneumonia, group B", "pneumonia; streptoccocal, group B", "Pneumonia due to Streptococcus Group B", "Pneumonia due to Streptococcus, group b", "Pneumonia due to Streptococcus, group B", "Pneumonia due to streptococcus, group B", "Group B streptococcal pneumonia (disorder)", "group B streptococcal pneumonia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Group B streptococcal pneumonia", "shortest_name_length": 7}
{"curie": "UMLS:C1334036", "names": ["Hodgkin-like PTLD", "Hodgkin's-like PTLD", "Hodgkin lymphoma - like PTLD", "Hodgkin-Like Post-Transplant Lymphoproliferative Disorder", "Hodgkin's-Like Post-Transplant Lymphoproliferative Disorder", "Hodgkin lymphoma-like post-transplant lymphoproliferative disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin-Like Post-Transplant Lymphoproliferative Disorder", "shortest_name_length": 17}
{"curie": "UMLS:C4744368", "names": ["Sellar ependymoma", "Sellar Ependymoma", "Ependymal Pituicytoma", "Sellar ependymoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sellar ependymoma", "shortest_name_length": 17}
{"curie": "MONDO:0700140", "names": ["Dog Osteosarcoma", "canine osteosarcoma", "Canine Osteosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canine osteosarcoma", "shortest_name_length": 16}
{"curie": "UMLS:C5420814", "names": ["Ciliary Body Nevus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ciliary Body Nevus", "shortest_name_length": 18}
{"curie": "UMLS:C4526972", "names": ["Stage IIIB Gastric and Omental GIST AJCC v8", "Stage IIIB Gastric and Omental Gastrointestinal Stromal Tumor AJCC v8", "Stage IIIB Gastric (Stomach) and Omental Gastrointestinal Stromal Tumor (GIST)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Gastric and Omental Gastrointestinal Stromal Tumor AJCC v8", "shortest_name_length": 43}
{"curie": "UMLS:C4520724", "names": ["Stage III Soft Tissue Sarcoma", "Stage III Adult Sarcoma of Soft Tissue", "Stage III Adult Sarcoma of the Soft Tissue", "Stage III Adult Soft Tissue Sarcoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Adult Soft Tissue Sarcoma AJCC v7", "shortest_name_length": 29}
{"curie": "MONDO:0014843", "names": ["POF11", "PREMATURE OVARIAN FAILURE 11", "premature ovarian failure 11", "ERCC6 primary ovarian failure", "primary ovarian insufficiency 12", "primary ovarian insufficiency 11", "premature ovarian failure type 11", "premature ovarian failure 11; POF11", "primary ovarian failure caused by mutation in ERCC6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "premature ovarian failure 11", "shortest_name_length": 5}
{"curie": "UMLS:C1334018", "names": ["High Grade Paranasal Sinus Sarcoma", "High Grade Accessory Sinus Sarcoma", "High Grade Sarcoma of Accessory Sinus", "High Grade Sarcoma of Paranasal Sinus", "High Grade Sarcoma of the Paranasal Sinus", "High Grade Sarcoma of the Accessory Sinus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Paranasal Sinus Sarcoma", "shortest_name_length": 34}
{"curie": "MONDO:0005545", "names": ["Staphylococcus aureus", "staphylococcus; aureus", "aureus; Staphylococcus", "Staphylococcus aureus NOS", "Staphylococcus aureus infection", "Staphylococcus aureus Infection", "staphylococcus aureus infection", "Staphylococcus aureus Infections", "Staphylococcus aureus infections", "Staphylococcus aureus infection NOS", "Infection due to Staphylococcus aureus", "Infection caused by Staphylococcus aureus", "Staphylococcus aureus infection (diagnosis)", "Infection caused by Staphylococcus aureus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "staphylococcus aureus infection", "shortest_name_length": 21}
{"curie": "UMLS:C3272426", "names": ["Plexiform Fibromyxoma", "Gastric Plexiform Fibromyxoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Plexiform Fibromyxoma", "shortest_name_length": 21}
{"curie": "UMLS:C1961112", "names": ["Heart Decompensation", "decompensation; heart", "heart; decompensation", "Decompensation, Heart", "Decompensation cardiac", "DECOMPENSATION CARDIAC", "cardiac decompensation", "cardiac; decompensation", "decompensation; cardiac"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Heart Decompensation", "shortest_name_length": 20}
{"curie": "UMLS:C0433895", "names": ["spinal cord contusion", "Spinal Cord Contusion", "Cord Contusion, Spinal", "Contusion, Spinal Cord", "Spinal Cord Contusions", "spinal cord contusions", "Contusions, Spinal Cord", "Cord Contusions, Spinal", "Contusion of spinal cord", "injury spinal cord contusion", "Contusion of spinal cord (disorder)", "Contusion of spinal cord (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spinal Cord Contusion", "shortest_name_length": 21}
{"curie": "MONDO:0012141", "names": ["OFC6", "orofacial cleft 6", "IRF6 orofacial cleft", "susceptibility to orofacial cleft 6", "OROFACIAL CLEFT 6, SUSCEPTIBILITY TO", "orofacial cleft 6, susceptibility to", "orofacial cleft caused by mutation in IRF6", "cleft lip with or without cleft palate, nonsyndromic, 6", "CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orofacial cleft 6, susceptibility to", "shortest_name_length": 4}
{"curie": "UMLS:C4521730", "names": ["Stage I Esophageal Squamous Cell Cancer", "Postneoadjuvant Therapy Stage I Esophageal Squamous Cell Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postneoadjuvant Therapy Stage I Esophageal Squamous Cell Carcinoma AJCC v8", "shortest_name_length": 39}
{"curie": "MONDO:0008958", "names": ["KFS2", "Klippel-Feil syndrome 2", "Kfs, Autosomal Recessive", "Kfs, autosomal recessive", "KFS, AUTOSOMAL RECESSIVE", "Klippel Feil syndrome recessive type", "MEOX1 isolated Klippel-Feil syndrome", "Klippel-Feil Syndrome, Autosomal Recessive", "KLIPPEL-FEIL SYNDROME 2, AUTOSOMAL RECESSIVE", "Klippel-Feil syndrome 2, autosomal recessive", "Klippel-FEIL syndrome 2, autosomal recessive", "cervical vertebral fusion, autosomal recessive", "Cervical vertebral fusion, autosomal recessive", "CERVICAL VERTEBRAL FUSION, AUTOSOMAL RECESSIVE", "isolated Klippel-Feil syndrome caused by mutation in MEOX1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Klippel-Feil syndrome 2, autosomal recessive", "shortest_name_length": 4}
{"curie": "MONDO:0020252", "names": ["essential strabismus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "essential strabismus", "shortest_name_length": 20}
{"curie": "MONDO:0017580", "names": ["dup(11)p(15.4)", "trisomy 11p15.4", "11p15.4 microduplication syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "11p15.4 microduplication syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C3714514", "names": ["INFECTION", "Infection", "infection", "Infections", "infections", "Infection NOS", "infection (diagnosis)", "Infection and Infestation", "Infestation and Infection", "Infections and Infestations", "Infestations and Infections"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infection", "shortest_name_length": 9}
{"curie": "UMLS:C5544451", "names": ["Neuroinflammatory Disease", "Neuroinflammatory Disorder", "Neuroinflammatory Diseases", "Disease, Neuroinflammatory", "Disorder, Neuroinflammatory", "Neuroinflammatory Disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neuroinflammatory Diseases", "shortest_name_length": 25}
{"curie": "MONDO:0005996", "names": ["Whipworm", "whipworm", "whip worm", "WHIP WORM", "whipworms", "whip worms", "Trichuriasis", "Trichuriosis", "trichuriasis", "TRICHURIASIS", "Trichuriases", "whipping worms", "whipworm disease", "Whipworm disease", "Trichocephaliases", "trichocephaliasis", "TRICHOCEPHALIASIS", "Trichocephaliasis", "whipworm infection", "Whipworm Infection", "Whipworm infection", "Infection, Whipworm", "Trichuris infection", "Trichuris Infection", "Whipworm Infections", "Trichuris Infections", "Infections, Whipworm", "Infection, Trichuris", "Infections, Trichuris", "Infection by Trichuris", "Trichuriasis infection", "trichuriasis infection", "Trichuriasis - whipworm", "Trichuriasis (disorder)", "Infection due to Trichuris", "Trichuris trichiura Infection", "trichuris trichiura infection", "Trichuris trichiura infection", "whipworm (disease)(infection)", "Infection, Trichuris trichiura", "Trichuris trichiuria infection", "Trichuris trichiura; infection", "Trichuris trichiura Infections", "Infection by Trichuris trichura", "Infections, Trichuris trichiura", "infection by Trichuris trichura", "Infection by Trichuris trichiura", "Infection by Trichuris trichiuria", "infection due to Trichuris trichiura", "Infection by Trichocephalus trichiura", "Infection due to Trichuris (diagnosis)", "Trichuris trichiura infectious disease", "Infection caused by Trichuris trichiura", "Trichuris trichiura disease or disorder", "Infection caused by Trichocephalus trichiura", "Trichuris trichiura caused disease or disorder", "infection due to Trichuris trichiura (diagnosis)", "Infection caused by Trichuris trichiura (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichuriasis", "shortest_name_length": 8}
{"curie": "UMLS:C5236008", "names": ["Genitourinary System Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Genitourinary System Carcinoma", "shortest_name_length": 30}
{"curie": "UMLS:C1336819", "names": ["Transverse Colon NET G1", "Transverse Colon Carcinoid Tumor", "Carcinoid Tumor of Transverse Colon", "Carcinoid Tumor of the Transverse Colon", "Transverse Colon Neuroendocrine Tumor G1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transverse Colon Neuroendocrine Tumor G1", "shortest_name_length": 23}
{"curie": "MONDO:0003743", "names": ["heart spindle cell tumor", "heart hemangiopericytoma", "heart malignant hemangiopericytoma", "malignant heart hemangiopericytoma", "Malignant Heart Hemangiopericytoma", "malignant Cardiac hemangiopericytoma", "Malignant Cardiac Hemangiopericytoma", "Malignant Hemangiopericytoma of Heart", "malignant hemangiopericytoma of Heart", "malignant hemangiopericytoma of heart", "Malignant Hemangiopericytoma of the Heart", "malignant hemangiopericytoma of the heart"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heart malignant hemangiopericytoma", "shortest_name_length": 24}
{"curie": "MONDO:0010238", "names": ["DFN6", "DFNX4", "X-linked deafness 4", "X-Linked Deafness-4", "Deafness, X-Linked 4", "deafness, X-linked 4", "DEAFNESS, X-LINKED 4", "hearing loss, X-linked 4", "deafness, X-linked type 4", "DEAFNESS, X-LINKED 4 (disorder)", "X-linked progressive deafness 6", "deafness, X-linked 6, progressive", "DEAFNESS, X-LINKED 6, PROGRESSIVE", "Deafness, X-Linked 6, Progressive", "SMPX X-linked nonsyndromic deafness", "deafness, X-linked 4, X-linked dominant", "nonsyndromic sensorineural progressive deafness 6", "DEAFNESS, NONSYNDROMIC SENSORINEURAL PROGRESSIVE 6", "Deafness, Nonsyndromic Sensorineural Progressive 6", "deafness, nonsyndromic sensorineural progressive 6", "X-linked nonsyndromic deafness caused by mutation in SMPX"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, X-linked 4", "shortest_name_length": 4}
{"curie": "MONDO:0014096", "names": ["WOODS SYNDROME", "WOODS syndrome", "Woods syndrome", "Woods-Crouchman-Huson syndrome", "microcephaly-intellectual disability-phalangeal and neurological anomalies syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly-intellectual disability-phalangeal and neurological anomalies syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C5670691", "names": ["Immunodeficiency-Related Central Nervous System Lymphoma", "Immunodeficiency-Associated Central Nervous System Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immunodeficiency-Related Central Nervous System Lymphoma", "shortest_name_length": 56}
{"curie": "MONDO:0014143", "names": ["NS8", "Noonan Syndrome 8", "Noonan syndrome 8", "NOONAN SYNDROME 8", "RIT1 Noonan syndrome", "Noonan syndrome type 8", "Noonan syndrome caused by mutation in RIT1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Noonan syndrome 8", "shortest_name_length": 3}
{"curie": "MONDO:0016648", "names": ["EDM", "MED", "polyepiphyseal dysplasia", "Polyepiphyseal dysplasia", "Multiple epiphyseal dysplasia", "Multiple Epiphyseal Dysplasia", "Dysplasia epiphyseal multiple", "multiple epiphyseal dysplasia", "DYSPLASIA EPIPHYSEAL MULTIPLE", "epiphyseal dysplasia, multiple", "MED - Multiple epiphyseal dysplasia", "Multiple epiphyseal dysplasia syndrome", "multiple epiphyseal dysplasia (disease)", "Multiple epiphyseal dysplasia (disorder)", "multiple epiphyseal dysplasia (diagnosis)", "Fairbanks-Ribbing type epiphyseal dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple epiphyseal dysplasia", "shortest_name_length": 3}
{"curie": "MONDO:0100385", "names": ["AML, t(11;19)(q23;p13.3)", "AML, t(11;19)(q23.3;p13.3)", "acute myeloid leukemia, t(11;19)(q23.3;p13.3)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, t(11;19)(q23.3;p13.3)", "shortest_name_length": 24}
{"curie": "UMLS:C4745071", "names": ["Metastatic Human Papillomavirus-Related Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Human Papillomavirus-Related Malignant Neoplasm", "shortest_name_length": 58}
{"curie": "MONDO:0700119", "names": ["distal 18q-", "distal 18q deletion", "distal 18q deletion syndrome", "distal chromosome 18q deletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal chromosome 18q deletion syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0011886", "names": ["DYT13", "torsion dystonia 13", "DYSTONIA 13, TORSION", "Dystonia 13, Torsion", "Primary dystonia type 13", "torsion dystonia type 13", "Primary dystonia DYT13 type", "primary dystonia, DYT13 type", "Primary dystonia, DYT13 type", "Primary dystonia type 13 (disorder)", "primary dystonia with mixed phenotype", "Primary dystonia with mixed phenotype", "DYSTONIA 13, TORSION, AUTOSOMAL DOMINANT", "dystonia 13, torsion, autosomal dominant", "Primary torsion dystonia with predominant craniocervical or upper limb onset", "primary torsion dystonia with predominant craniocervical or upper limb onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "torsion dystonia 13", "shortest_name_length": 5}
{"curie": "MONDO:0011465", "names": ["infundibulocystic basal cell carcinoma", "Infundibulocystic basal cell carcinoma", "Infundibulocystic Basal Cell Carcinoma", "basal cell carcinoma, infundibulocystic", "BASAL CELL CARCINOMA, INFUNDIBULOCYSTIC", "Basal cell carcinoma, infundibulocystic", "Skin Infundibulocystic Basal Cell Carcinoma", "skin infundibulocystic basal cell carcinoma", "BASAL CELL CARCINOMA WITH FOLLICULAR DIFFERENTIATION", "Basal cell carcinoma with follicular differentiation", "basal cell carcinoma with follicular differentiation", "Basal cell carcinoma with follicular differentiation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infundibulocystic basal cell carcinoma", "shortest_name_length": 38}
{"curie": "MONDO:0020411", "names": ["aorto-left ventricular tunnel"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aorto-left ventricular tunnel", "shortest_name_length": 29}
{"curie": "UMLS:C4289310", "names": ["FIGO Stage IVB Ovarian Cancer", "FIGO Stage IVB Ovarian Carcinoma", "stage IVB ovarian epithelial cancer", "Stage IVB Ovarian Epithelial Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Stage IVB Ovarian Cancer", "shortest_name_length": 29}
{"curie": "UMLS:C3897084", "names": ["Stage IIIA Esophageal Cancer", "Stage IIIA Esophageal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Esophageal Cancer AJCC v7", "shortest_name_length": 28}
{"curie": "MONDO:0007078", "names": ["AHO", "PHP1a", "PHPIa", "PHP1A", "PHP 1A", "PHP Ia", "PHP IA", "AHO-PHP syndrome Ia", "pseudohypoparathyroidism Ia", "pseudo hypoparathyroidism IA", "Pseudohypoparathyroidism Type 1a", "pseudohypoparathyroidism type 1A", "Pseudohypoparathyroidism type Ia", "Pseudohypoparathyroidism type 1A", "pseudohypoparathyroidism type 1a", "Type Ia Pseudohypoparathyroidism", "pseudohypoparathyroidism type ia", "Pseudohypoparathyroidism type I A", "PSEUDOHYPOPARATHYROIDISM, TYPE IA", "pseudohypoparathyroidism, type IA", "pseudohypoparathyroidism, type 1A", "Pseudohypoparathyroidism, Type IA", "Pseudohypoparathyroidism, Type Ia", "Type Ia Pseudohypoparathyroidisms", "Albright Hereditary Osteodystrophy", "Albright hereditary osteodystrophy", "Pseudohypoparathyroidisms, Type Ia", "Osteodystrophy, Albright Hereditary", "Hereditary Osteodystrophy, Albright", "Albright's hereditary osteodystrophy", "Albright's Hereditary Osteodystrophy", "OSTEODYSTROPHY, HEREDITARY OF ALBRIGHT", "AHO - Albright hereditary osteodystrophy", "pseudo hypoparathyroidism IA (diagnosis)", "Pseudohypoparathyroidism type I A (disorder)", "[OBSOLETE] Albright's hereditary osteodystrophy", "Albright hereditary osteodystrophy, classical type", "Albright hereditary osteodystrophy-PHP syndrome Ia", "Albright hereditary osteodystrophy with multiple hormone resistance", "ALBRIGHT HEREDITARY OSTEODYSTROPHY WITH MULTIPLE HORMONE RESISTANCE", "Albright Hereditary Osteodystrophy with Multiple Hormone Resistance", "Albright's Hereditary Osteodystrophy with Multiple Hormone Resistance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudohypoparathyroidism type 1A", "shortest_name_length": 3}
{"curie": "UMLS:C4331996", "names": ["Cerebellar, Fourth Ventricle, and Brain Stem Ependymal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebellar, Fourth Ventricle, and Brain Stem Ependymal Tumor", "shortest_name_length": 60}
{"curie": "MONDO:0014749", "names": ["STHAG7", "LRP6 tooth agenesis", "tooth agenesis, selective, 7", "TOOTH AGENESIS, SELECTIVE, 7", "tooth agenesis, selective, type 7", "tooth agenesis, selective, 7; STHAG7", "tooth agenesis caused by mutation in LRP6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tooth agenesis, selective, 7", "shortest_name_length": 6}
{"curie": "UMLS:C0281641", "names": ["M0 Adult AML", "M0 Adult ANLL", "Adult Acute M0 Leukemia", "adult acute M0 leukemia", "M0 Adult Acute Leukemia", "M0 leukemia, adult acute", "M0 Adult Acute Myelocytic Leukemia", "M0 Adult Acute Myelogenous Leukemia", "M0 Adult Acute Myeloblastic Leukemia", "Adult Acute Myeloid Leukemia Minimally Differentiated", "M0 Undifferentiated OR AML with minimal differentiation", "M0 adult acute minimally differentiated myeloid leukemia", "Adult Acute Myeloid Leukemia with Minimal Differentiation", "Acute Myeloid Leukemia (AML) with Minimal Differentiation", "Adult Acute Minimally Differentiated Myeloid Leukemia (M0)", "adult acute minimally differentiated myeloid leukemia (M0)", "M0 Adult Acute Myeloid Leukemia with Minimal Differentiation", "Adult Acute Myelocytic Leukemia with Minimal Differentiation", "Adult Acute Myelogenous Leukemia with Minimal Differentiation", "Adult Acute Myeloblastic Leukemia with Minimal Differentiation", "Adult Acute Granulocytic Leukemia with Minimal Differentiation", "M0 Adult Acute Myelocytic Leukemia with Minimal Differentiation", "M0 Adult Acute Myelogenous Leukemia with Minimal Differentiation", "M0 Adult Acute Myeloblastic Leukemia with Minimal Differentiation", "M0 Adult Acute Granulocytic Leukemia with Minimal Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Acute Myeloid Leukemia with Minimal Differentiation", "shortest_name_length": 12}
{"curie": "UMLS:C0272448", "names": ["Muscle/Tendon Damage", "injury musculoskeletal", "MUSCULOSKELETAL INJURY", "Musculoskeletal injury", "Injury;musculoskeletal", "Musculoskeletal Injury", "musculoskeletal injury", "injuries musculoskeletal", "Injury musculoskeletal nos", "Other musculoskeletal injury", "Injury of musculoskeletal system", "injury of musculoskeletal system", "INJURIES OF THE MUSCULOSKELETAL SYSTEM", "Injury of musculoskeletal system (disorder)", "injury of musculoskeletal system (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of musculoskeletal system", "shortest_name_length": 20}
{"curie": "UMLS:C0280174", "names": ["Stage IV Diffuse Mixed Cell Lymphoma", "Adult Diffuse Mixed Cell Lymphoma Stage IV", "stage IV adult diffuse mixed cell lymphoma", "Stage IV Adult Diffuse Mixed Cell Lymphoma", "adult diffuse mixed cell lymphoma, stage IV", "metastatic adult diffuse mixed cell lymphoma", "adult diffuse mixed cell lymphoma, metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Adult Diffuse Mixed Cell Lymphoma", "shortest_name_length": 36}
{"curie": "MONDO:0009847", "names": ["cholesterol pericarditis", "Cholesterol Pericarditis", "CHOLESTEROL PERICARDITIS", "Pericardial Effusion, Chronic", "pericardial effusion, chronic", "PERICARDIAL EFFUSION, CHRONIC", "chronic pericardial effusion (disease)", "pericardial effusion (disease), chronic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pericardial effusion, chronic", "shortest_name_length": 24}
{"curie": "UMLS:C4525622", "names": ["Stage II Ampulla of Vater Neuroendocrine Tumor", "Stage II Ampulla of Vater Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Ampulla of Vater Neuroendocrine Tumor AJCC v8", "shortest_name_length": 46}
{"curie": "MONDO:0032630", "names": ["MC1DN26", "nuclear type mitochondrial complex I deficiency 26", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 26", "mitochondrial complex 1 deficiency, nuclear type 26"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 26", "shortest_name_length": 7}
{"curie": "MONDO:0002829", "names": ["Bartholin Gland Cancer", "Bartholin gland cancer", "bartholin's gland cancer", "Bartholin's Gland Cancer", "Bartholin's gland cancer", "bartholin's cancer gland", "Bartholin gland carcinoma", "bartholin gland carcinoma", "Bartholin Gland Carcinoma", "Bartholin's gland carcinoma", "Bartholin's Gland Carcinoma", "Carcinoma of Bartholin gland", "Carcinoma of Bartholin's gland", "Carcinoma of Bartholin's Gland", "carcinoma of Bartholin's gland", "major vestibular gland carcinoma", "Carcinoma of the Bartholin's Gland", "carcinoma of the Bartholin's gland", "Bartholin gland carcinoma (disease)", "carcinoma of major vestibular gland", "Carcinoma of Bartholin's gland (disorder)", "Carcinoma of Bartholin's gland (diagnosis)", "Bartholin's gland carcinoma (morphologic abnormality)", "vulvar neoplasm malignant Bartholin's gland carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bartholin gland carcinoma", "shortest_name_length": 22}
{"curie": "UMLS:C0234447", "names": ["Narcosis", "narcosis", "Narcosis, NOS", "Narcosis (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Narcosis", "shortest_name_length": 8}
{"curie": "MONDO:0019986", "names": ["sporadic idiopathic steroid-resistant nephrotic syndrome with collapsing glomerulopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sporadic idiopathic steroid-resistant nephrotic syndrome with collapsing glomerulopathy", "shortest_name_length": 87}
{"curie": "UMLS:C2018769", "names": ["Splenic Follicular Lymphoma", "follicular lymphoma of spleen", "Primary Splenic Follicular Lymphoma", "follicular lymphoma of spleen (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "follicular lymphoma of spleen", "shortest_name_length": 27}
{"curie": "MONDO:0007524", "names": ["EDS 4", "EDSVASC", "vascular type Ehlers-Danlos syndrome", "Ehlers-Danlos syndrome, arterial type", "Ehlers-Danlos syndrome, vascular type", "Ehlers-Danlos syndrome, Ecchymotic type", "Ehlers-Danlos syndrome, sack-Barabas type", "autosomal dominant type IV Ehlers-Danlos syndrome", "Ehlers-Danlos syndrome, type IV, autosomal dominant", "autosomal dominant Ehlers-Danlos syndrome, vascular type", "Ehlers-Danlos syndrome, vascular type, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant Ehlers-Danlos syndrome, vascular type", "shortest_name_length": 5}
{"curie": "MONDO:0800093", "names": ["dysostosis with brachydactyly without extraskeletal manifestations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dysostosis with brachydactyly without extraskeletal manifestations", "shortest_name_length": 66}
{"curie": "MONDO:0017579", "names": ["BRWS", "Fryns-Aftimos syndrome", "Baraitser-winter syndrome", "Baraitser-Winter syndrome", "trigonocephaly ptosis coloboma", "cerebro-frontofacial syndrome, type 3", "trigonocephaly ptosis mental retardation", "Baraitser-Winter cerebrofrontofacial syndrome", "trigonocephaly ptosis intellectual disability", "iris coloboma with ptosis hypertelorism and mental retardation", "iris coloboma with ptosis hypertelorism and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Baraitser-Winter cerebrofrontofacial syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0100444", "names": ["NFRCD", "RLBP1 retinopathy", "fundus albipunctatus", "Vasterbotten dystrophy", "Västerbotten dystrophy", "RLBP1 cone-rod dystrophy", "Bothnia retinal dystrophy", "RLBP1-related retinopathy", "retinitis punctata albescens", "pigmentary retinal dystrophy", "Newfoundland rod-cone dystrophy", "Newfoundland ROD-cone dystrophy", "cone-rod dystrophy caused by mutation in RLBP1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "RLBP1-related retinopathy", "shortest_name_length": 5}
{"curie": "MONDO:0006172", "names": ["Conjunctival nevus", "Conjunctival Nevus", "conjunctival nevus", "Conjunctival naevus", "Nevus of Conjunctiva", "Nevus of conjunctiva", "Naevus of conjunctiva", "nevus; site conjunctiva", "Nevus of the Conjunctiva", "Nevus of the conjunctiva", "Nevus of conjunctiva (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "conjunctival nevus", "shortest_name_length": 18}
{"curie": "UMLS:C5239031", "names": ["Metastatic Myxofibrosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Myxofibrosarcoma", "shortest_name_length": 27}
{"curie": "UMLS:C2938980", "names": ["Postictal psychosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postictal psychosis", "shortest_name_length": 19}
{"curie": "UMLS:C0840564", "names": ["Bladder rupture", "bladder rupture", "rupture bladder", "BLADDER RUPTURE", "bladder; rupture", "ruptured bladder", "Ruptured bladder", "Rupture of bladder", "rupture of bladder", "Urinary bladder rupture", "Rupture of bladder, NOS", "Rupture of bladder (disorder)", "rupture of bladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rupture of bladder", "shortest_name_length": 15}
{"curie": "UMLS:C0855236", "names": ["Disturbance in social behavior", "Disturbance in social behaviour", "Socialized disturbance of conduct", "Socialised disturbance of conduct", "Disturbance in social behavior NOS", "Disturbance in social behaviour NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disturbance in social behavior", "shortest_name_length": 30}
{"curie": "MONDO:0003997", "names": ["colon Kaposi sarcoma", "Colon Kaposi Sarcoma", "Colon Kaposis Sarcoma", "colon Kaposis sarcoma", "Colonic Kaposi Sarcoma", "colonic Kaposi sarcoma", "colon Kaposi's sarcoma", "Colon Kaposi's Sarcoma", "colonic Kaposis sarcoma", "Kaposi sarcoma of colon", "Colonic Kaposis Sarcoma", "colonic Kaposi's sarcoma", "Colonic Kaposi's sarcoma", "Colonic Kaposi's Sarcoma", "Kaposi's Sarcoma of Colon", "Kaposi's sarcoma of colon", "Kaposi's Sarcoma of the Colon", "Kaposi's sarcoma of the colon", "colon Kaposi's sarcoma (disease)", "Kaposi sarcoma of colon (disorder)", "Kaposi's sarcoma (disease) of colon", "Kaposi's sarcoma of colon (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colon Kaposi sarcoma", "shortest_name_length": 20}
{"curie": "MONDO:0018795", "names": ["syndromic constitutional thrombocytopenia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic constitutional thrombocytopenia", "shortest_name_length": 41}
{"curie": "MONDO:0010875", "names": ["PACHYDERMODACTYLY, FAMILIAL", "pachydermodactyly, familial", "Pachydermodactyly, Familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pachydermodactyly, familial", "shortest_name_length": 27}
{"curie": "UMLS:C0267919", "names": ["Primary cholangitis", "primary cholangitis", "Primary cholangitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary cholangitis", "shortest_name_length": 19}
{"curie": "UMLS:C0920563", "names": ["Insulin Sensitivity", "insulin sensitivity", "Sensitivity, Insulin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Insulin Sensitivity", "shortest_name_length": 19}
{"curie": "UMLS:C2984900", "names": ["PHEOCHROMOCYTOMA, COMPLEX, MALIGNANT", "Malignant Adrenal Gland Composite Pheochromocytoma", "Metastatic Adrenal Gland Composite Pheochromocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Adrenal Gland Composite Pheochromocytoma", "shortest_name_length": 36}
{"curie": "MONDO:0009180", "names": ["JEB-I", "JEB-nH", "JEN-nH", "Epidermolysis Bullosa Progressiva", "Epidermolysis bullosa progressiva", "junctional epidermolysis bullosa inversa", "Junctional epidermolysis bullosa progressiva", "EPIDERMOLYSIS BULLOSA JUNCTIONALIS, PROGRESSIVE", "Epidermolysis Bullosa Junctionalis, Progressive", "epidermolysis bullosa Junctionalis, progressive", "epidermolysis bullosa Junctionalis, Disentis type", "epidermolysis bullosa, generalized atrophic benign", "junctional epidermolysis bullosa, non-Herlitz type", "epidermolysis bullosa, junctional, non-Herlitz type", "epidermolysis bullosa Junctionalis, non-Herlitz type", "epidermolysis bullosa Junctionalis, severe Nonlethal", "epidermolysis bullosa, junctional, Localisata variant", "Progressive junctional epidermolysis bullosa (neurotrophic)", "Progressive junctional epidermolysis bullosa (neurotrophic) (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "junctional epidermolysis bullosa, non-Herlitz type", "shortest_name_length": 5}
{"curie": "MONDO:0009298", "names": ["GOMBO syndrome", "GOMBO SYNDROME", "GROWTH RETARDATION, OCULAR ABNORMALITIES, MICROCEPHALY, BRACHYDACTYLY, AND OLIGOPHRENIA", "Growth retardation, ocular abnormalities, microcephaly, brachydactyly, and oligophrenia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "GOMBO syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0021146", "names": ["chronic headache", "headache disorder", "HEADACHE DISORDER", "chronic headaches", "Headache Disorder", "headache, chronic", "headache syndrome", "Headache disorder", "Headache Syndrome", "headache syndromes", "Syndrome, Headache", "headache disorders", "Headache Disorders", "Headache Syndromes", "syndrome, headache", "headaches, chronic", "headache; syndrome", "cephalgia syndrome", "syndrome; headache", "Cephalgia Syndrome", "disorders headache", "headaches syndrome", "cephalgia syndromes", "Cephalgia Syndromes", "disorders headaches", "headaches syndromes", "intractable headache", "intractable headaches", "headache, intractable", "chronic daily headache", "headaches, intractable", "chronic daily headaches", "headache, chronic daily", "daily headache, chronic", "daily headaches, chronic", "headaches, chronic daily", "Headache disorder (disorder)", "headache syndromes (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "headache disorder", "shortest_name_length": 16}
{"curie": "MONDO:0010076", "names": ["SEMDIT", "SEMD, Irapa type", "Spondyloepimetaphyseal dysplasia Irapa type", "Irapa type spondyloepimetaphyseal dysplasia", "Spondyloepimetaphyseal Dysplasia, Irapa Type", "SPONDYLOEPIMETAPHYSEAL DYSPLASIA, IRAPA TYPE", "spondyloepimetaphyseal dysplasia, Irapa type", "Spondyloepimetaphyseal dysplasia, Irapa type", "Autosomal recessive spondyloepimetaphyseal dysplasia", "Spondyloepimetaphyseal dysplasia Irapa type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepimetaphyseal dysplasia, Irapa type", "shortest_name_length": 6}
{"curie": "UMLS:C1334651", "names": ["Mediastinal Choriocarcinoma", "choriocarcinoma of mediastinum", "Choriocarcinoma of Mediastinum", "Choriocarcinoma of the Mediastinum", "anterior mediastinal choriocarcinoma", "choriocarcinoma of mediastinum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choriocarcinoma of mediastinum", "shortest_name_length": 27}
{"curie": "UMLS:C5556794", "names": ["Metastatic Vaginal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Vaginal Squamous Cell Carcinoma", "shortest_name_length": 42}
{"curie": "UMLS:C0333472", "names": ["Epidermolysis", "epidermolysis", "Epidermolysis, NOS", "Epidermolysis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epidermolysis", "shortest_name_length": 13}
{"curie": "MONDO:0007885", "names": ["Lcp", "LCP", "LCPD", "Perthes", "COXA PLANA", "coxa plana", "Coxa Plana", "Coxa plana", "plana; coxa", "coxa; plana", "Legg-Perthes", "Calvé-Perthes", "perthe disease", "pseudocoxalgia", "Pseudocoxalgia", "disease perthes", "perthes disease", "Perthes disease", "PERTHES DISEASE", "Perthes Disease", "perthe's disease", "perthes' disease", "Disease, Perthes", "Perthe's disease", "disease perthes's", "legg perthe disease", "disease legg perthe", "Legg Perthes Disease", "Legg-Perthes disease", "perthes legg disease", "legg-perthes disease", "LEGG-PERTHES DISEASE", "legg perthes disease", "Legg-Perthes Disease", "Legg Perthes disease", "Disease, Legg-Perthes", "Disease;Calve-Perthes", "Coxa plana (disorder)", "disease leggs perthes", "Calve-Perthes disease", "Perthes disease of hip", "Perthe's disease of hip", "Calve - Perthes' disease", "Osteochondritis Deforman", "calve disease legg perthe", "Morbus Legg-Calve-Perthes", "osteochondritis deformans", "legg calve perthe disease", "disease legg calve perthe", "Osteochondritis Deformans", "disease legg calve perthes", "Legg-Calvé-Perthes Disease", "Legg Calve Perthes Disease", "LEGG-CALVE-PERTHES DISEASE", "Legg-Calvé-Perthes disease", "legg-calve-perthes disease", "Legg-Calve-Perthes Disease", "Legg-CALVE-Perthes disease", "Legg Calve Perthes disease", "disease legg-calve-perthes", "legg calve perthes disease", "calve disease legg perthes", "disease legg calves perthe", "Legg-Calve-Perthes symptom", "Legg Calvé Perthes Disease", "Legg-Calve-Perthes disease", "legg perthes calve disease", "calve diseases legg perthes", "Legg-Calvé-Perthes Syndrome", "Legg Calve Perthes Syndrome", "Legg Calvé Perthes Syndrome", "disease legg calves perthes", "Legg-Calve-Perthes Syndrome", "LEGG-CALVE-PERTHES SYNDROME", "legg-calve-perthes syndrome", "Disease, Legg-Calve-Perthes", "Legg-Calve-Perthes syndrome", "Disease, Legg-Calvé-Perthes", "Syndrome, Legg-Calvé-Perthes", "Syndrome, Legg-Calve-Perthes", "juvenile osteochond-hip/pelvis", "Juvenile osteochond-hip/pelvis", "Juvenile osteochondrosis of hip", "Osteonecrosis of the femoral head", "Perthes-like femoral head changes", "Osteochondrosis of the femoral head", "Osteochondrosis of Legg-Calve-Perthes", "osteochondrosis of Legg-Calve-Perthes", "Legg-Calve-Perthes disease (diagnosis)", "head of femur; juvenile osteochondrosis", "head of femur; osteochondrosis, juvenile", "osteochondrosis; juvenile, head of femur", "Juvenile osteochondrosis of head of femur", "osteochondrosis; femoral capital epiphysis", "femoral capital epiphysis; osteochondrosis", "Juvenile osteochondrosis of hip and pelvis", "juvenile osteochondrosis of hip and pelvis", "OSTEOCHONDROSIS, CAPITAL FEMORAL EPIPHYSIS", "Aseptic necrosis of capital femoral epiphysis", "Juvenile osteochondrosis of hip AND/OR pelvis", "Juvenile osteochondrosis of hip and/or pelvis", "juvenile osteochondrosis of hip and/or pelvis", "osteochondritis of the capital femoral epiphysis", "Osteochondrosis of the capital femoral epiphysis", "aseptic necrosis of the capital femoral epiphysis", "Aseptic necrosis of the capital femoral epiphysis", "epiphysis; juvenile osteochondrosis head of femur", "Avascular necrosis of the capital femoral epiphysis", "Perthes disease - osteochondritis of the femoral head", "Perthes' disease - osteochondritis of the femoral head", "Juvenile osteochondrosis of head of femur [Legg-Calvé-Perthes]", "Avascular necrosis of the capital femoral epiphysis (disorder)", "Juvenile osteochondrosis of head of femur [Legg-Calve-Perthes]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Legg-Calve-Perthes disease", "shortest_name_length": 3}
{"curie": "UMLS:C1332466", "names": ["Benign Adult Brain Tumor", "Benign Tumor of Adult Brain", "Benign Adult Brain Neoplasm", "Benign Neoplasm of Adult Brain", "Brain Neoplasms, Adult, Benign", "Benign Tumor of the Adult Brain", "Benign Neoplasm of the Adult Brain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Adult Brain Neoplasm", "shortest_name_length": 24}
{"curie": "UMLS:C3160840", "names": ["Macular pigmentation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Macular pigmentation", "shortest_name_length": 20}
{"curie": "MONDO:0010553", "names": ["Charcot-Marie-Tooth Peroneal Muscular Atrophy and Friedreich Ataxia, Combined", "CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA, COMBINED", "Charcot-Marie-Tooth peroneal muscular atrophy and Friedreich ataxia, combined"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth peroneal muscular atrophy and Friedreich ataxia, combined", "shortest_name_length": 77}
{"curie": "MONDO:0030723", "names": ["DFNA83", "DEAFNESS, AUTOSOMAL DOMINANT 83", "deafness, autosomal dominant 83", "hearing loss, autosomal dominant 83"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal dominant 83", "shortest_name_length": 6}
{"curie": "UMLS:C4727782", "names": ["Advanced Non-Small Cell Squamous Lung Cancer", "Advanced Non-Small Cell Squamous Lung Carcinoma", "Advanced Squamous Non-Small Cell Lung Carcinoma", "Advanced Lung Non-Small Cell Squamous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Lung Non-Small Cell Squamous Carcinoma", "shortest_name_length": 44}
{"curie": "MONDO:0015562", "names": ["17q monosomy", "monosomy 17q", "17q deletion", "deletion 17q", "monosomy 17qter", "Monosomy 17qter", "Distal 17q deletion", "distal monosomy 17q", "Distal monosomy 17q", "distal 17q deletion", "partial monosomy 17q", "Telomeric deletion 17q", "telomeric deletion 17q", "chromosome 17q deletion", "distal monosomy type 17q", "Distal monosomy 17q (disorder)", "Deletion of long arm of chromosome 17", "deletion of part of chromosome 17 long arm", "Deletion of long arm of chromosome 17 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal monosomy 17q", "shortest_name_length": 12}
{"curie": "UMLS:C4727190", "names": ["Refractory Liver Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Liver Carcinoma", "shortest_name_length": 26}
{"curie": "UMLS:C4285348", "names": ["FIGO Stage IIIB Ovarian Cancer", "FIGO Stage IIIB Ovarian Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Stage IIIB Ovarian Cancer", "shortest_name_length": 30}
{"curie": "UMLS:C2713499", "names": ["Total Hexosaminidase Deficiency", "Deficiency, Total Hexosaminidase", "Hexosaminidase Deficiency, Total", "Total Hexosaminidase Deficiencies", "beta Hexosaminidase beta Subunit Deficiency", "beta-Hexosaminidase-beta-Subunit Deficiency", "Deficiency, beta-Hexosaminidase-beta-Subunit", "beta-Hexosaminidase-beta-Subunit Deficiencies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Total Hexosaminidase Deficiency", "shortest_name_length": 31}
{"curie": "UMLS:C1520079", "names": ["Vulvar Dysplastic Melanocytic Nevus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Dysplastic Melanocytic Nevus", "shortest_name_length": 35}
{"curie": "MONDO:0019050", "names": ["Hemoglobinopathy", "HEMOGLOBINOPATHY", "hemoglobinopathy", "Haemoglobinopathy", "haemoglobinopathy", "Hemoglobin disease", "Hemoglobinopathies", "hemoglobinopathies", "hemoglobin disease", "Globin abnormality", "HEMOGLOBINOPATHIES", "Hemoglobin disorder", "haemoglobin disease", "hemoglobin disorder", "diseases hemoglobin", "Haemoglobin disease", "haemoglobinopathies", "Haemoglobinopathies", "HEMOGLOBIN DISORDER", "Hemoglobinopathy NOS", "hemoglobin disorders", "Haemoglobin disorder", "Hemoglobin disorders", "disorders hemoglobin", "Hemoglobinopathy, NOS", "Haemoglobinopathy NOS", "Haemoglobinopathy, NOS", "Hemoglobin disease, NOS", "Globin abnormality, NOS", "Haemoglobin disease, NOS", "Hemoglobin disorder, NOS", "Haemoglobin disorder, NOS", "inherited hemoglobinopathy", "Hemoglobinopathy (disorder)", "hereditary hemoglobinopathy", "Hereditary hemoglobinopathy", "Hereditary haemoglobinopathy", "hemoglobinopathy (diagnosis)", "Hemoglobinopathies congenital", "Haemoglobinopathies congenital", "Hemoglobinopathies / iron metabolism", "Hemoglobinopathies / Iron Metabolism", "Hereditary hemoglobinopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited hemoglobinopathy", "shortest_name_length": 16}
{"curie": "MONDO:0005563", "names": ["NMC", "NUT carcinoma", "NUT Carcinoma", "NUT midline carcinoma", "nut midline carcinoma", "NUT Midline Carcinoma", "NUT Midline carcinoma", "Nuclear protein in testis carcinoma", "NUT (nuclear protein in testis) carcinoma", "NUT midline carcinoma of the head and neck", "nuclear protein in testis midline carcinoma", "Nuclear Protein in Testis Midline Carcinoma", "Nuclear protein in testis associated carcinoma", "Nuclear protein in testis carcinoma (disorder)", "Carcinoma with t(15;19)(q13;p13.1) Translocation", "carcinoma with t(15;19)(q13;p13.1) translocation", "Nuclear Protein in Testis (NUT) Midline Carcinoma", "NUT (nuclear protein in testis) midline carcinoma", "Midline carcinoma of children and Young adults with NUT rearrangement", "Midline carcinoma of children and young adults with NUT rearrangement", "midline carcinoma of children and young adults with NUT rearrangement", "Midline Carcinoma of Children and Young Adults with NUT Rearrangement", "Nuclear protein in testis associated carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nut midline carcinoma", "shortest_name_length": 3}
{"curie": "OMIM:619030", "names": ["SMGMQTL", "SKELETAL MUSCLE GLYCOGEN CONTENT AND METABOLISM QUANTITATIVE TRAIT LOCUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 7}
{"curie": "UMLS:C4553161", "names": ["Recurrent Anaplastic Oligodendroglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Anaplastic Oligodendroglioma", "shortest_name_length": 38}
{"curie": "MONDO:0003825", "names": ["ROCY", "Renal oncocytoma", "Renal Oncocytoma", "renal oncocytoma", "oncocytoma renal", "Kidney Oncocytoma", "kidney oncocytoma", "Oncocytoma, renal", "oncocytoma kidney", "Oncocytoma of kidney", "oncocytoma of kidney", "Oncocytoma of Kidney", "Oncocytoma of the Kidney", "oncocytoma of the kidney", "kidney oncocytic neoplasm", "benign oncocytoma of kidney", "Oncocytoma of kidney (disorder)", "Renal Epithelial Oncocytic Tumor", "renal epithelial oncocytic tumor", "renal epithelial Oncocytic tumor", "renal epithelial oncocytic neoplasm", "Renal Epithelial Oncocytic Neoplasm", "benign oncocytoma of kidney (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kidney oncocytoma", "shortest_name_length": 4}
{"curie": "UMLS:C4763561", "names": ["Borderline Resectable Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Resectable Carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0011593", "names": ["BFIC2", "BFIS2", "benign familial infantile seizures 2", "Benign Familial Infantile Seizures, 2", "SEIZURES, BENIGN FAMILIAL INFANTILE, 2", "Seizures, Benign Familial Infantile, 2", "seizures, benign familial infantile, 2", "convulsions, benign familial infantile, 2", "Convulsions, Benign Familial Infantile, 2", "CONVULSIONS, BENIGN FAMILIAL INFANTILE, 2", "seizures, benign familial infantile, type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "seizures, benign familial infantile, 2", "shortest_name_length": 5}
{"curie": "UMLS:C0752206", "names": ["Sporadic Dystonia", "Dystonia, Sporadic", "Sporadic Dystonias", "Dystonias, Sporadic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dystonias, Sporadic", "shortest_name_length": 17}
{"curie": "UMLS:C2064401", "names": ["Undifferentiated Liver Cancer", "Undifferentiated Liver Carcinoma", "Liver Undifferentiated Carcinoma", "undifferentiated carcinoma of liver", "Undifferentiated Primary Liver Carcinoma", "undifferentiated carcinoma of liver (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "undifferentiated carcinoma of liver", "shortest_name_length": 29}
{"curie": "UMLS:C0581386", "names": ["ANXIETY CHRONIC", "chronic anxiety", "anxiety chronic", "Chronic anxiety", "Chronic anxiety (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic anxiety", "shortest_name_length": 15}
{"curie": "MONDO:0014438", "names": ["BBS10", "Bardet-Biedl syndrome 10", "Bardet-Biedl Syndrome 10", "BARDET-BIEDL SYNDROME 10", "BBS10 Bardet-Biedl syndrome", "Bardet-Biedl syndrome type 10", "Bardet-Biedl syndrome caused by mutation in BBS10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bardet-Biedl syndrome 10", "shortest_name_length": 5}
{"curie": "MONDO:0002856", "names": ["Gallbladder Rhabdomyosarcoma", "gallbladder rhabdomyosarcoma", "gall bladder rhabdomyosarcoma", "rhabdomyosarcoma of gallbladder", "Rhabdomyosarcoma of Gallbladder", "rhabdomyosarcoma of the gallbladder", "Rhabdomyosarcoma of the Gallbladder", "Rhabdomyosarcoma of the gallbladder", "gall bladder rhabdomyosarcoma (disease)", "rhabdomyosarcoma (disease) of gall bladder", "rhabdomyosarcoma of gallbladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gallbladder rhabdomyosarcoma", "shortest_name_length": 28}
{"curie": "MONDO:0016709", "names": ["Anaplastic large cell medulloblastoma", "Large Cell/Anaplastic Medulloblastoma", "anaplastic/large cell medulloblastoma", "large cell/anaplastic medulloblastoma", "Anaplastic/large cell medulloblastoma", "Anaplastic large cell medulloblastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anaplastic/large cell medulloblastoma", "shortest_name_length": 37}
{"curie": "UMLS:C3854439", "names": ["Procedural anxiety"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Procedural anxiety", "shortest_name_length": 18}
{"curie": "UMLS:C0003621", "names": ["Appetite Disorder", "Appetite disorder", "appetite disorder", "Appetite disorders", "Appetite Disorders", "Appetite disorder NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Appetite Disorders", "shortest_name_length": 17}
{"curie": "MONDO:0003444", "names": ["Intrahepatic Bile Duct Adenoma", "intrahepatic bile duct adenoma", "adenoma; intrahepatic bile duct", "intrahepatic; adenoma bile duct", "adenoma; bile duct, intrahepatic", "bile duct; adenoma, intrahepatic", "Adenoma of Intrahepatic Bile Duct", "adenoma of intrahepatic bile duct", "adenoma of the Intrahepatic bile duct", "Adenoma of the Intrahepatic Bile Duct", "adenoma of the intrahepatic bile duct", "adenoma, HEPATOCHOLANGIOCELLULAR, benign", "ADENOMA, HEPATOCHOLANGIOCELLULAR, BENIGN", "adenoma of intrahepatic bile duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intrahepatic bile duct adenoma", "shortest_name_length": 30}
{"curie": "MONDO:0020556", "names": ["pleuropulmonary blastoma type 2", "type II pleuropulmonary blastoma", "Type II Pleuropulmonary Blastoma", "Pleuropulmonary blastoma type II", "Pleuro-pulmonary blastoma type II", "Pleuropulmonary blastoma type II (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pleuropulmonary blastoma type 2", "shortest_name_length": 31}
{"curie": "MONDO:0019478", "names": ["adult NLPHD", "Adult NLPHD", "nodular lymphocyte predominant Hodgkin lymphoma", "Nodular Lymphocyte Predominant Hodgkin Lymphoma", "adult nodular lymphocyte predominant Hodgkin lymphoma", "Adult Nodular Lymphocyte Predominant Hodgkin Lymphoma", "adult nodular lymphocyte predominant Hodgkin's disease", "Adult Nodular Lymphocyte Predominant Hodgkin's Disease", "Adult Nodular Lymphocyte Predominant Hodgkin's Lymphoma", "adult nodular lymphocyte predominant Hodgkin's lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult nodular lymphocyte predominant Hodgkin lymphoma", "shortest_name_length": 11}
{"curie": "MONDO:0011931", "names": ["OVCAS1", "ovarian cancer, susceptibility to", "ovarian cancer, susceptibility to, 1", "OVARIAN CANCER, SUSCEPTIBILITY TO, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian cancer, susceptibility to, 1", "shortest_name_length": 6}
{"curie": "MONDO:0015310", "names": ["syndromic optic nerve hypoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic optic nerve hypoplasia", "shortest_name_length": 32}
{"curie": "MONDO:0004354", "names": ["neonatal leukemia", "Leukemia neonatal", "Neonatal leukemia", "Neonatal Leukemia", "LEUKEMIA NEONATAL", "Leukaemia neonatal", "Neonatal leukaemia", "LEUKAEMIA NEONATAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal leukemia", "shortest_name_length": 17}
{"curie": "MONDO:0006193", "names": ["benign endometrial hyperplasia", "Benign endometrial hyperplasia", "Typical endometrial hyperplasia", "Typical Endometrial Hyperplasia", "typical endometrial hyperplasia", "endometrial hyperplasia - benign", "Endometrial Hyperplasia without Atypia", "endometrial hyperplasia without atypia", "Endometrial hyperplasia without atypia", "Benign endometrial hyperplasia (disorder)", "benign endometrial hyperplasia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometrial hyperplasia without atypia", "shortest_name_length": 30}
{"curie": "MONDO:0018949", "names": ["distal myopathy", "Distal myopathy", "Distal Myopathy", "Myopathy, Distal", "distal; myopathy", "Myopathy, distal", "myopathy; distal", "Distal Myopathies", "Myopathies, Distal", "Distal Muscular Dystrophy", "distal muscular dystrophy", "DISTAL MUSCULAR DYSTROPHY", "Distal muscular dystrophy", "MUSCULAR DYSTROPHY, DISTAL", "Muscular dystrophy, distal", "Muscular Dystrophy, Distal", "Miyoshi muscular dystrophy", "muscular; dystrophy, distal", "dystrophy; muscular, distal", "Distal Muscular Dystrophies", "Muscular Dystrophies, Distal", "Distal muscular dystrophy (disorder)", "distal muscular dystrophy (diagnosis)", "distal progressive muscular dystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal myopathy", "shortest_name_length": 15}
{"curie": "MONDO:0001192", "names": ["Esophagus Melanoma", "esophagus melanoma", "Esophageal Melanoma", "oesophagus melanoma", "esophageal melanoma", "Melanoma of Esophagus", "melanoma of esophagus", "melanoma of oesophagus", "melanoma of the esophagus", "Melanoma of the Esophagus", "esophagus melanoma (disease)", "melanoma (disease) of esophagus", "mucosal melanoma of the esophagus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophageal melanoma", "shortest_name_length": 18}
{"curie": "MONDO:0017551", "names": ["humero-radial fusion, bilateral", "humero-radial synostosis, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "humero-radial synostosis, bilateral", "shortest_name_length": 31}
{"curie": "MONDO:0018536", "names": ["adenocarcinoma of gallbladder and EBT", "adenocarcinoma of the gallbladder and EBT", "Adenocarcinoma of the gallbladder and EBT", "adenocarcinoma of gallbladder and extrahepatic biliary tract", "Adenocarcinoma of gallbladder and extrahepatic biliary tract", "adenocarcinoma of the gallbladder and extrahepatic biliary tract", "Adenocarcinoma of the gallbladder and extrahepatic biliary tract", "Adenocarcinoma of gallbladder and extrahepatic biliary tract (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenocarcinoma of gallbladder and extrahepatic biliary tract", "shortest_name_length": 37}
{"curie": "MONDO:0004217", "names": ["Childhood Brain Germinoma", "pediatric brain germinoma", "Pediatric Brain Germinoma", "childhood brain germinoma", "germinoma of pediatric brain", "germinoma of childhood brain", "Germinoma of Pediatric Brain", "brain germinoma of childhood", "Germinoma of Childhood Brain", "Pediatric Brain Germ Cell Cancer", "Germinoma of the Childhood Brain", "germinoma of the childhood brain", "pediatric brain germ cell cancer", "Germinoma of the Pediatric Brain", "germinoma of the pediatric brain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood brain germinoma", "shortest_name_length": 25}
{"curie": "MONDO:0005755", "names": ["EIA", "Swamp fever", "Swamp Fever", "Fever, Swamp", "Swamp Fevers", "Fevers, Swamp", "swamp fever of horses", "equine infectious anemia", "Equine Infectious Anemia", "Equine infectious anemia", "Anemia, Equine Infectious", "Equine Infectious Anemias", "Equine infectious anaemia", "Infectious Anemia, Equine", "Anemias, Equine Infectious", "Infectious Anemias, Equine", "EIA - equine infectious anemia", "equine infectious anemia (EIA)", "EIA - equine infectious anaemia", "Equine infectious anemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "equine infectious anemia", "shortest_name_length": 3}
{"curie": "UMLS:C1519703", "names": ["Turcot Syndrome Type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Turcot Syndrome Type 2", "shortest_name_length": 22}
{"curie": "UMLS:C0281914", "names": ["Musculoskeletal Deformity", "Musculoskeletal deformity", "musculoskeletal deformity", "MUSCULOSKELETAL DEFORMITY, NOS", "musculoskeletal deformity (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Musculoskeletal Deformity", "shortest_name_length": 25}
{"curie": "MONDO:0004022", "names": ["parasagittal meningioma", "Parasagittal Meningioma", "Meningioma, Parasagittal", "Parasagittal Meningiomas", "Meningiomas, Parasagittal", "parasagittal meningioma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parasagittal meningioma", "shortest_name_length": 23}
{"curie": "MONDO:0015377", "names": ["Third branchial cleft cyst", "third branchial cleft cyst", "Type 3 branchial cleft cyst", "third branchial cleft fistula", "Third branchial cleft anomaly", "third branchial cleft anomaly", "Third branchial cleft fistula", "Third branchial cleft cyst (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "third branchial cleft anomaly", "shortest_name_length": 26}
{"curie": "UMLS:C0541435", "names": ["Brachial Plexus Palsy", "brachial plexus palsy", "palsy brachial plexus", "Palsy, brachial plexus", "paralysis brachial plexus", "brachial plexus paralysis", "Paralysis, brachial plexus", "brachial plexus; paralysis", "paralysis; brachial plexus", "plexus brachialis; paralysis", "Palsies of the Brachial Plexus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brachial Plexus Palsy", "shortest_name_length": 21}
{"curie": "MONDO:0016837", "names": ["dup(16)(p13.11)", "Dup(16)(p13.11)", "trisomy 16p13.11", "Trisomy 16p13.11", "16p13.11 microduplication syndrome", "16p13.11 microduplication syndrome (disorder)", "16p13.11 recurrent microduplication (neurocognitive disorder susceptibility locus)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "16p13.11 microduplication syndrome", "shortest_name_length": 15}
{"curie": "UMLS:C0022360", "names": ["deformity jaw", "jaw deformity", "JAW DEFORMITY", "deformity; jaw", "jaw; deformity", "Jaw Abnormality", "abnormality jaw", "deformities jaw", "jaw abnormality", "Abnormality, Jaw", "jaw abnormalities", "Jaw Abnormalities", "abnormalities jaw", "Abnormalities, Jaw", "Jaws--Abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jaw Abnormalities", "shortest_name_length": 13}
{"curie": "UMLS:C0151977", "names": ["ulcer small intestine", "intestine small ulcer", "ULCER SMALL INTESTINE", "SMALL INTESTINE ULCER", "Ulcer small intestine", "Small intestine ulcer", "Small Intestinal Ulcer", "intestine small ulcers", "Small intestinal ulcer NOS", "SMALL INTESTINAL ULCER NOS", "ulceration of small intestine", "Ulceration of small intestine", "Ulceration of small intestine (disorder)", "ulceration of small intestine (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Intestinal Ulcer", "shortest_name_length": 21}
{"curie": "UMLS:C0036981", "names": ["Endotoxic shock", "Endotoxin Shock", "endotoxic shock", "endotoxic; shock", "shock; endotoxic", "Shock, Endotoxic", "Shock, Endotoxin", "Endotoxin Shocks", "Shock, endotoxic", "Shocks, Endotoxin", "Gram-negative shock", "gram negative shock", "Endotoxic septic shock", "Shock due to endotoxin", "Endotoxic shock (disorder)", "gram-negative septic shock", "Gram-negative septic shock", "Gram-negative septic shock (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endotoxic shock", "shortest_name_length": 15}
{"curie": "MONDO:0014604", "names": ["PARK21", "Parkinson disease 21", "PARKINSON DISEASE 21", "Parkinson's disease 21", "Parkinson disease type 21", "DNAJC13 hereditary late onset Parkinson disease", "hereditary late onset Parkinson disease caused by mutation in DNAJC13"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parkinson disease 21", "shortest_name_length": 6}
{"curie": "UMLS:C1334023", "names": ["High Risk Colorectal Gastrointestinal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Risk Colorectal Gastrointestinal Stromal Tumor", "shortest_name_length": 51}
{"curie": "UMLS:C0338457", "names": ["Progressive aphasia", "Progressive Aphasia", "Progressive Aphasias", "Aphasia, Progressive", "Progressive aphasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aphasia, Progressive", "shortest_name_length": 19}
{"curie": "MONDO:0021765", "names": ["RADICULITIS", "Radiculitis", "radiculitis", "Radiculitides", "Radiculitis NOS", "radiculitis nos", "Radiculitis, NOS", "Radiculitis (disorder)", "nerve root inflammation", "radiculitis (diagnosis)", "Nerve Root Inflammation", "Inflammation, Nerve Root", "Nerve Root Inflammations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radiculitis", "shortest_name_length": 11}
{"curie": "UMLS:C4290035", "names": ["46,XX True Hermaphroditism", "46,XX Ovotesticular Difference of Sex Development"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XX Ovotesticular Difference of Sex Development", "shortest_name_length": 26}
{"curie": "MONDO:0001903", "names": ["Milwaukee shoulder", "calcific tendonitis", "Calcific tendinitis", "TENDONITIS CALCIFIC", "calcific tendinitis", "Calcific tendonitis", "TENDINITIS, CALCIFIC", "calcific; tendinitis", "tendinitis; calcific", "calcified tendinitis", "calcifying tendinitis", "Calcific tendinitis NOS", "Calcific tendinitis, NOS", "calcific tendonitis shoulder", "shoulder calcific tendonitis", "calcific tendinitis shoulder", "shoulder calcific tendinitis", "calcific shoulder tendinitis", "SHOULDER TENDONITIS CALCIFIC", "calcific shoulder tendonitis", "calcifying tendinitis shoulder", "tendinitis; calcific, shoulder", "calcifying shoulder tendinitis", "Calcific tendinitis (disorder)", "Calcific tendinitis of shoulder", "calcific tendonitis of shoulder", "Calcific tendonitis of shoulder", "calcific tendonitis (diagnosis)", "Calcifying tendinitis of shoulder", "Calcifying tendinitis of the shoulder", "Calcific tendinitis of shoulder (disorder)", "calcific tendonitis of shoulder (diagnosis)", "Apatite-associated destructive arthritis of shoulder", "Apatite-associated destructive arthritis of shoulder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "calcific tendinitis", "shortest_name_length": 18}
{"curie": "UMLS:C0677710", "names": ["Stage II Burkitt Lymphoma", "noncontiguous stage II adult Burkitt lymphoma", "Stage II Non-Contiguous Adult Burkitt Lymphoma", "Stage II Non-Contiguous Adult Burkitt's Lymphoma", "Ann Arbor Stage II Non-Contiguous Adult Burkitt Lymphoma", "Non-Contiguous Adult Diffuse Small Non-Cleaved Cell Lymphoma Stage II", "Stage II Non-Contiguous Adult Diffuse Small Non-Cleaved Cell Lymphoma", "noncontiguous stage II adult diffuse small noncleaved cell/Burkitt's lymphoma", "Stage II Non-Contiguous Adult Diffuse Small Non-Cleaved Cell/Burkitt's Lymphoma", "Non-Contiguous Adult Diffuse Small Non-Cleaved Cell/Burkitt's Lymphoma Stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage II Non-Contiguous Adult Burkitt Lymphoma", "shortest_name_length": 25}
{"curie": "UMLS:C4054066", "names": ["Renal Tubular Acidosis Associated With Deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal Tubular Acidosis Associated With Deafness", "shortest_name_length": 47}
{"curie": "UMLS:C0152437", "names": ["Placenta Polyp", "polyp; placenta", "Placental polyp", "placental polyp", "Placental Polyp", "placenta; polyp", "Polyp of Placenta", "polyp of placenta", "Polyp of the Placenta", "Placental polyp (disorder)", "placental polyp (diagnosis)", "polyp of placenta (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Placental polyp", "shortest_name_length": 14}
{"curie": "UMLS:C5419587", "names": ["Recurrent Grade 3b Follicular Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Grade 3b Follicular Lymphoma", "shortest_name_length": 38}
{"curie": "UMLS:C5556595", "names": ["EGFRI-Induced Acneiform Rash", "EGFRI-Induced Acneiform Lesion", "EGFRI-Induced Acneiform Dermatitis", "Epidermal Growth Factor Receptor Inhibitor-Induced Acneiform Rash", "Epidermal Growth Factor Receptor Inhibitor-Induced Acneiform Lesion", "Epidermal Growth Factor Receptor Inhibitor-Induced Acneiform Dermatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epidermal Growth Factor Receptor Inhibitor-Induced Acneiform Lesion", "shortest_name_length": 28}
{"curie": "MONDO:0012305", "names": ["PPR3", "photoparoxysmal response 3", "PHOTOPAROXYSMAL RESPONSE 3", "Photoparoxysmal Response 3", "Photoparoxysmal Response With Or Without Myoclonic Epilepsy", "PHOTOPAROXYSMAL RESPONSE WITH OR WITHOUT MYOCLONIC EPILEPSY", "photoparoxysmal response with or without myoclonic epilepsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "photoparoxysmal response 3", "shortest_name_length": 4}
{"curie": "MONDO:0020661", "names": ["Undifferentiated Ewing Tumor", "undifferentiated round cell sarcoma", "Undifferentiated round cell sarcoma", "Undifferentiated Round Cell Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "undifferentiated round cell sarcoma", "shortest_name_length": 28}
{"curie": "UMLS:C4524518", "names": ["Tumor Stage (Pathological)", "Cutaneous Squamous Cell Carcinoma of the Head and Neck by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous Squamous Cell Carcinoma of the Head and Neck by AJCC v8 Stage", "shortest_name_length": 26}
{"curie": "MONDO:0014582", "names": ["CMS2C", "congenital myasthenic syndrome 2C", "congenital myasthenic syndrome type 2C", "congenital myasthenic syndrome 2C associated with acetylcholine receptor deficiency", "MYASTHENIC SYNDROME, CONGENITAL, 2C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY", "myasthenic syndrome, congenital, 2C, associated with acetylcholine receptor deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myasthenic syndrome 2C", "shortest_name_length": 5}
{"curie": "UMLS:C1963824", "names": ["Shortened cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Shortened cervix", "shortest_name_length": 16}
{"curie": "UMLS:C0751645", "names": ["Inherited Human Transmissible Spongiform Encephalopathies", "Human Transmissible Spongiform Encephalopathies, Inherited"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Human Transmissible Spongiform Encephalopathies, Inherited", "shortest_name_length": 57}
{"curie": "MONDO:0013643", "names": ["HNFJ3", "HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 3", "hyperuricemic nephropathy, familial juvenile, 3", "hyperuricemic nephropathy, familial juvenile type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperuricemic nephropathy, familial juvenile type 3", "shortest_name_length": 5}
{"curie": "MONDO:0006704", "names": ["CNS demyelinating autoimmune disease", "CNS Demyelinating Autoimmune Diseases", "Demyelinating Disease, Autoimmune, CNS", "CNS Autoimmune Demyelinating Disorders", "Autoimmune Demyelinating Diseases, CNS", "Demyelinating Autoimmune Diseases, CNS", "Autoimmune Demyelinating Disorders, CNS", "Demyelinating Autoimmune Disorders, CNS", "Autoimmune Demyelinating Diseases, Central Nervous System", "Demyelinating Autoimmune Diseases, Central Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CNS demyelinating autoimmune disease", "shortest_name_length": 36}
{"curie": "UMLS:C5555185", "names": ["Refractory Ovarian Undifferentiated Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Ovarian Undifferentiated Carcinoma", "shortest_name_length": 45}
{"curie": "UMLS:C5205700", "names": ["Head and Neck Small Cell Carcinoma", "Head and Neck Small Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Head and Neck Small Cell Neuroendocrine Carcinoma", "shortest_name_length": 34}
{"curie": "UMLS:C0521853", "names": ["Drug tolerance increased", "Increased drug tolerance", "Increased drug tolerance (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Increased drug tolerance", "shortest_name_length": 24}
{"curie": "MONDO:0012120", "names": ["PDHPD", "PDH phosphatase deficiency", "pyruvate dehydrogenase phosphatase deficiency", "PYRUVATE DEHYDROGENASE PHOSPHATASE DEFICIENCY", "Pyruvate dehydrogenase phosphatase deficiency", "Pyruvate dehydrogenase phosphatase deficiency (disorder)", "LACTIC ACIDEMIA WITH PYRUVATE DEHYDROGENASE PHOSPHATASE DEFICIENCY", "lactic acidemia with pyruvate dehydrogenase phosphatase deficiency", "Lactic acidemia with pyruvate dehydrogenase phosphatase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyruvate dehydrogenase phosphatase deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C1336333", "names": ["Stage IVA Bone Sarcoma", "Stage IVA Sarcoma of Bone", "Stage IVA Sarcoma of the Bone", "Stage IVA Bone Sarcoma AJCC v7", "Stage IVA Bone Sarcoma  AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Bone Sarcoma AJCC v7", "shortest_name_length": 22}
{"curie": "MONDO:0015626", "names": ["CMT", "CMT/HMSN", "CHARCOT-MARIE-TOOTH", "Marie-Charcot-Tooth", "Charcot-Marie-Tooth", "Charcot-Marie Disease", "Charcot Marie Disease", "Peroneal muscular atrophy", "peroneal muscular atrophy", "Peroneal Muscular Atrophy", "PERONEAL MUSCULAR ATROPHY", "Atrophy, Peroneal Muscular", "Muscular Atrophy, Peroneal", "Charcot-Marie-Tooth Disease", "charcot-marie-tooth disease", "CHARCOT MARIE TOOTH DISEASE", "Charcot Marie Tooth Disease", "Atrophy, Muscular, Peroneal", "CHARCOT-MARIE-TOOTH ATROPHY", "charcot marie tooth disease", "Charcot-Marie-Tooth disease", "Peroneal Muscular Atrophies", "Charcot Marie Tooth disease", "Charcot-Marie-Tooth; atrophy", "Atrophies, Peroneal Muscular", "charcot marie tooth syndrome", "Muscular Atrophies, Peroneal", "Charcot-Marie-Tooth syndrome", "atrophy; Charcot-Marie-Tooth", "Charcot-Marie-Tooth Syndrome", "Charcot Marie Tooth Syndrome", "charcot-marie-tooth syndrome", "Syndrome, Charcot-Marie-Tooth", "CMT - Charcot-Marie-Tooth disease", "Hereditary Sensorimotor Neuropathy", "Peroneal muscular atrophy syndrome", "hereditary sensorimotor neuropathy", "Charcot Marie Tooth muscular atrophy", "Hereditary Motor and Sensory Neuropathy", "Charcot-Marie-Tooth disease (diagnosis)", "hereditary motor and sensory neuropathy", "Charcot-Marie-Tooth Hereditary Neuropathy", "Charcot Marie Tooth Hereditary Neuropathy", "Charcot-Marie-Tooth hereditary neuropathy", "Hereditary Neuropathy, Charcot-Marie-Tooth", "Charcot-Marie-Tooth disease/hereditary motor and sensory neuropathy", "Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease", "shortest_name_length": 3}
{"curie": "EFO:0011023", "names": ["concussion\"@e"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "concussion\"@e", "shortest_name_length": 13}
{"curie": "OMIM:609027", "names": [], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"]}
{"curie": "UMLS:C1332626", "names": ["Metastatic Breast Cancer in the Lung", "Breast Carcinoma Metastatic in the Lung", "Breast Carcinoma Metastatic to the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Carcinoma Metastatic in the Lung", "shortest_name_length": 36}
{"curie": "MONDO:0005488", "names": ["scoliosis; adolescence", "adolescence; scoliosis", "scoliosis idiopathic adolescent", "Adolescent idiopathic scoliosis", "idiopathic adolescent scoliosis", "adolescent idiopathic scoliosis", "Adolescent idiopathic scoliosis (disorder)", "adolescent idiopathic scoliosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adolescent idiopathic scoliosis", "shortest_name_length": 22}
{"curie": "UMLS:C0235511", "names": ["Superficial vein thrombosis", "superficial vein thrombosis", "superficial thrombosis vein", "Superficial phlebothrombosis", "SUPERFICIAL VENOUS THROMBOSIS", "THROMBOSIS VENOUS SUPERFICIAL", "superficial venous thrombosis", "Thrombosis venous superficial", "Superficial thrombosis of veins", "Superficial vein thrombosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Superficial vein thrombosis", "shortest_name_length": 27}
{"curie": "MONDO:0017448", "names": ["digits 2-5 hypodactyly", "digits 2-5 oligodactyly", "congenital absence/hypoplasia of fingers excluding thumb"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital absence/hypoplasia of fingers excluding thumb", "shortest_name_length": 22}
{"curie": "UMLS:C5236972", "names": ["Soft Tissue Sarcoma of the Trunk and Extremities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Soft Tissue Sarcoma of the Trunk and Extremities", "shortest_name_length": 48}
{"curie": "MONDO:0004477", "names": ["Adrenal Ganglioneuroblastoma", "adrenal ganglioneuroblastoma", "Adrenal Gland Ganglioneuroblastoma", "adrenal gland ganglioneuroblastoma", "adrenal gland ganglioneuroblastoma (disease)", "malignant ganglioneuroblastoma of adrenal gland", "ganglioneuroblastoma (disease) of adrenal gland", "malignant ganglioneuroblastoma of adrenal gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adrenal gland ganglioneuroblastoma", "shortest_name_length": 28}
{"curie": "MONDO:0020485", "names": ["KDS", "KING SYNDROME", "King syndrome", "King-Denborough Syndrome", "Koussef-Nichols syndrome", "KING-DENBOROUGH SYNDROME", "King Denborough syndrome", "Koussef Nichols syndrome", "King-Denborough syndrome", "Kousseff Nichols syndrome", "King Denborough syndrome (disorder)", "King-Denborough syndrome (diagnosis)", "Noonan like contracture myopathy hyperpyrexia", "anesthetic-induced malignant hyperpyrexia in children"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "King-Denborough syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C3272793", "names": ["FSA", "Filiform Serrated Adenoma", "Digestive System Filiform Serrated Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Filiform Serrated Adenoma", "shortest_name_length": 3}
{"curie": "MONDO:0020860", "names": ["faucial diphtheria", "diphtheria; throat", "Faucial Diphtheria", "Faucial diphtheria", "Diphtheria, faucial", "Diphtheritic membrane", "pharynx; diphtheritic", "diphtheritic membrane", "Pharyngeal diphtheria", "diphtheritic; sore throat", "sore throat; diphtheritic", "diphtheritic; pharyngitis", "pharyngitis; diphtheritic", "Faucial diphtheria (disorder)", "Diphtheritic membranous angina", "faucial diphtheria (diagnosis)", "diphtheritic membranous angina", "membranous; angina, diphtheritic", "angina; membranous, diphtheritic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "faucial diphtheria", "shortest_name_length": 18}
{"curie": "UMLS:C2985307", "names": ["Maternal Hypotension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Maternal Hypotension", "shortest_name_length": 20}
{"curie": "UMLS:C1515988", "names": ["Aneuploid Dysplastic Oral Leukoplakia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aneuploid Dysplastic Oral Leukoplakia", "shortest_name_length": 37}
{"curie": "UMLS:C5555298", "names": ["Current Seasonal Coronavirus Infection", "Current_Seasonal_Coronavirus_infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Current Seasonal Coronavirus Infection", "shortest_name_length": 38}
{"curie": "UMLS:C3899621", "names": ["Circumscribed Morphea"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Circumscribed Morphea", "shortest_name_length": 21}
{"curie": "MONDO:0002434", "names": ["oculomotor nerve cancer", "cancer of oculomotor nerve", "malignant oculomotor nerve tumor", "malignant oculomotor nerve neoplasm", "Malignant Oculomotor Nerve Neoplasm", "oculomotor nerve neoplasm, malignant", "Oculomotor Nerve Neoplasm, Malignant", "malignant neoplasm of oculomotor nerve", "Malignant neoplasm of oculomotor nerve", "IIIrd cranial nerve neoplasm, malignant", "IIIrd Cranial Nerve Neoplasm, Malignant", "IIIrd Cranial nerve neoplasm, malignant", "primary malignant neoplasm of oculomotor nerve", "Primary malignant neoplasm of oculomotor nerve", "Primary malignant neoplasm of oculomotor nerve (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculomotor nerve cancer", "shortest_name_length": 23}
{"curie": "UMLS:C1279420", "names": ["anxiety state", "state anxiety", "Anxiety Neuroses", "neurosis anxiety", "anxiety neurosis", "Anxiety neurosis", "Anxiety Neurosis", "ANXIETY/NEUROSIS", "ANXIETY NEUROSIS", "neurosis; anxiety", "Neurosis, anxiety", "Neuroses, Anxiety", "anxiety; neurosis", "Anxiety neurosis (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anxiety neurosis (finding)", "shortest_name_length": 13}
{"curie": "UMLS:C3495874", "names": ["Nonepileptic Seizure", "nonepileptic seizures", "Non-epileptic seizure", "Seizure, Nonepileptic", "Non-Epileptic Seizure", "Non Epileptic Seizure", "Nonepileptic Seizures", "Non-Epileptic Seizures", "Non Epileptic Seizures", "Seizures, Nonepileptic", "Seizure, Non-Epileptic", "nonepileptic seizures (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nonepileptic Seizures", "shortest_name_length": 20}
{"curie": "UMLS:C4727684", "names": ["Metastatic Oral Cavity Squamous Cell Cancer", "Metastatic Oral Cavity Squamous Cell Carcinoma", "Metastatic Squamous Cell Carcinoma of the Oral Cavity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Oral Cavity Squamous Cell Carcinoma", "shortest_name_length": 43}
{"curie": "UMLS:C4683230", "names": ["Retinoblastoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retinoblastoma by AJCC v8 Stage", "shortest_name_length": 31}
{"curie": "UMLS:C0747772", "names": ["postnatal complication", "Complication;postnatal", "Postpartum complication", "complication postpartum", "POSTPARTUM COMPLICATION", "Postpartum Complication", "postpartum complication", "complications postpartum", "postpartum complications"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postpartum Complication", "shortest_name_length": 22}
{"curie": "MONDO:0021652", "names": ["diffuse type carcinoma", "Diffuse Type Carcinoma", "Carcinoma, diffuse type", "Carcinoma - diffuse type", "Diffuse Type Adenocarcinoma", "diffuse type adenocarcinoma", "Adenocarcinoma, diffuse type", "Adenocarcinoma - diffuse type", "carcinoma; diffuse type, unspecified site", "diffuse; carcinoma (type), unspecified site", "Carcinoma, diffuse type (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diffuse type adenocarcinoma", "shortest_name_length": 22}
{"curie": "UMLS:C2242588", "names": ["Traumatic liver injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Traumatic liver injury", "shortest_name_length": 22}
{"curie": "MONDO:0054728", "names": ["SPGF24", "spermatogenic failure 24", "SPERMATOGENIC FAILURE 24"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 24", "shortest_name_length": 6}
{"curie": "MONDO:0002140", "names": ["vagina sarcoma", "Vagina Sarcoma", "VAGINA, SARCOMA", "vaginal sarcoma", "Vaginal Sarcoma", "Sarcoma of Vagina", "sarcoma of vagina", "sarcoma of the vagina", "Sarcoma of the Vagina", "VAGINAL CANCER, SARCOMA", "sarcoma of vagina (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vagina sarcoma", "shortest_name_length": 14}
{"curie": "MONDO:0017901", "names": ["autosomal recessive MSMD due to partial IFNgammaR1 deficiency", "autosomal recessive MSMD due to partial interferon gamma receptor 1 deficiency", "IFNGR1 autosomal recessive mendelian susceptibility to mycobacterial diseases due to a partial deficiency", "autosomal recessive Mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency", "autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 1 deficiency", "autosomal recessive mendelian susceptibility to mycobacterial diseases due to a partial deficiency caused by mutation in IFNGR1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive Mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency", "shortest_name_length": 61}
{"curie": "UMLS:C0334059", "names": ["Moderate epithelial dysplasia", "Moderate Epithelial Dysplasia", "Grade 2 Intraepithelial Neoplasia", "Grade II Intraepithelial Neoplasia", "Moderate epithelial dysplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Moderate epithelial dysplasia", "shortest_name_length": 29}
{"curie": "MONDO:0007803", "names": ["MSA", "Shy-Drager", "Shy-Drager Syndrome", "shy-drager syndrome", "Multisystem atrophy", "multisystem atrophy", "Multisystem Atrophy", "Shy-Drager syndrome", "Shy Drager Syndrome", "shy drager syndrome", "Shy Drager syndrome", "SHY-DRAGER SYNDROME", "shy dragers syndrome", "Atrophy, Multisystem", "Syndrome, Shy-Drager", "dragers shy syndrome", "Multisystemic Atrophy", "Multisystem Atrophies", "Atrophy, Multisystemic", "Atrophies, Multisystem", "Multiple System Atrophy", "autonomic failure, Pure", "multiple system atrophy", "Multisystemic Atrophies", "atrophy multiple system", "Multiple system atrophy", "atrophy multiple systems", "Atrophies, Multisystemic", "Atrophy, Multiple System", "hypotension, orthostatic", "Multiple System Atrophies", "Progressive autonomic failure", "Autonomic failure progressive", "MSA - Multiple system atrophy", "Progressive Autonomic Failure", "Progressive Autonomic Failures", "Autonomic Failure, Progressive", "Failure, Progressive Autonomic", "Failures, Progressive Autonomic", "Shy-Drager syndrome (diagnosis)", "multisystem atrophy (diagnosis)", "Autonomic Failures, Progressive", "Shy-dragger syndrome (formerly)", "Multiple System Atrophy Syndrome", "Multiple system atrophy (disorder)", "Dysautonomic Orthostatic Hypotension", "Dysautonomic Orthostatic Hypotensions", "Hypotension, Dysautonomic Orthostatic", "Orthostatic Hypotension, Dysautonomic", "Orthostatic Hypotensions, Dysautonomic", "Hypotensions, Dysautonomic Orthostatic", "susceptibility to multiple system atrophy 1", "Dysautonomia Orthostatic Hypotension Syndrome", "Orthostatic hypotension dysautonomic syndrome", "Dysautonomia-Orthostatic Hypotension Syndrome", "Syndrome, Dysautonomia Orthostatic Hypotension", "Syndrome, Dysautonomia-Orthostatic Hypotension", "Dysautonomia-Orthostatic Hypotension Syndromes", "Hypotension Syndrome, Dysautonomia-Orthostatic", "Hypotension Syndromes, Dysautonomia-Orthostatic", "Syndromes, Dysautonomia-Orthostatic Hypotension", "Idiopathic Orthostatic Hypotension, Shy-Drager Type", "Idiopathic Orthostatic Hypotension, Shy Drager Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple system atrophy", "shortest_name_length": 3}
{"curie": "UMLS:C5418906", "names": ["Resectable Carcinoma of Unknown Primary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Carcinoma of Unknown Primary", "shortest_name_length": 39}
{"curie": "MONDO:0024464", "names": ["CPHD1", "pituitary hormone deficiency, combined 1", "PITUITARY HORMONE DEFICIENCY, COMBINED, 1", "Pituitary Hormone Deficiency, Combined, 1", "pituitary hormone deficiency, combined, 1", "pituitary hormone deficiency, combined or isolated, 1", "PITUITARY HORMONE DEFICIENCY, COMBINED OR ISOLATED, 1", "POU1F1 combined pituitary hormone deficiencies, genetic form", "combined pituitary hormone deficiencies, genetic form caused by mutation in POU1F1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pituitary hormone deficiency, combined, 1", "shortest_name_length": 5}
{"curie": "MONDO:0800045", "names": ["AISBL", "AIFBL", "AIFBL1", "A20 haploinsufficiency", "Behçet-like disease due to HA20", "hereditary pediatric Behçet-like disease", "familial Behcet-like autoinflammatory syndrome", "autoinflammatory syndrome, familial, Behcet-like", "AUTOINFLAMMATORY SYNDROME, FAMILIAL, BEHCET-LIKE 1", "autoinflammatory syndrome, familial, Behcet-like 1", "Behçet-like disease due to haploinsufficiency of A20"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoinflammatory syndrome, familial, Behcet-like 1", "shortest_name_length": 5}
{"curie": "UMLS:C0038819", "names": ["siriasis", "SIRIASIS", "Siriasis", "Sunstroke", "sunstroke", "SUNSTROKE", "stroke sun", "sunstrokes", "Sunstrokes", "Sun Stroke", "Sun stroke", "sun stroke", "SUN STROKE", "strokes sun", "Heat Stroke", "Sun Strokes", "ictus solaris", "Ictus solaris", "Sunstroke, NOS", "Sunstroke (disorder)", "sunstroke (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sunstroke", "shortest_name_length": 8}
{"curie": "UMLS:C4527180", "names": ["Stage II Cutaneous (Skin) Melanoma", "Pathologic Stage II Cutaneous Melanoma AJCC v8", "Pathologic Stage II Melanoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage II Cutaneous Melanoma AJCC v8", "shortest_name_length": 34}
{"curie": "UMLS:C1096458", "names": ["Vascular occlusion", "vascular occlusion", "vascular; occlusion", "occlusion; vascular", "occlusions vascular", "vascular obstruction", "Vascular obstruction", "blood vessel occlusion", "blood occlusion vessels", "Occlusion of blood vessel"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vascular occlusion", "shortest_name_length": 18}
{"curie": "UMLS:C4727219", "names": ["Metastatic Cervical Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Cervical Adenocarcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0001233", "names": ["tenonitis", "Tenonitis", "Orbital tenonitis", "orbital tenonitis", "Tenonitis (disorder)", "tenonitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orbital tenonitis", "shortest_name_length": 9}
{"curie": "MONDO:0004856", "names": ["Rosacea conjunctivitis", "rosacea conjunctivitis", "conjunctivitis rosacea", "Rosacea conjunctivitis (disorder)", "Rosacea conjunctivitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rosacea conjunctivitis", "shortest_name_length": 22}
{"curie": "MONDO:0003668", "names": ["extragonadal seminoma", "Extragonadal Seminoma", "extragonadal primary seminoma", "Extragonadal Primary Seminoma", "Primary Extragonadal Seminoma", "primary extragonadal seminoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extragonadal seminoma", "shortest_name_length": 21}
{"curie": "MONDO:0800111", "names": ["PTI, usual", "persistent tachypnoe of infancy, usual"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "persistent tachypnoe of infancy, usual", "shortest_name_length": 10}
{"curie": "UMLS:C0037176", "names": ["Single-Gene Defect", "Single gene defect", "Defect, Single-Gene", "Single-Gene Defects", "Single Gene Defects", "Defects, Single-Gene", "Single gene defect (qualifier value)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Single-Gene Defects", "shortest_name_length": 18}
{"curie": "MONDO:0022817", "names": ["congenital amputation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital amputation", "shortest_name_length": 21}
{"curie": "MONDO:0001430", "names": ["deep corneal vascularisation", "Deep corneal vascularization", "Deep corneal vascularisation", "deep vascularization of cornea", "Deep vascularisation of cornea", "Deep vascularization of cornea", "Deep vascularization of cornea (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deep corneal vascularisation", "shortest_name_length": 28}
{"curie": "MONDO:0042451", "names": ["ENDOMYOMETRITIS", "endomyometritis", "Endomyometritis", "Endomyometritis, NOS", "Endomyometritis (disorder)", "endomyometritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endomyometritis", "shortest_name_length": 15}
{"curie": "UMLS:C3899667", "names": ["Ependymal Tumor", "Childhood Ependymal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Ependymal Tumor", "shortest_name_length": 15}
{"curie": "UMLS:C3897739", "names": ["Recurrent Extragonadal Seminoma", "recurrent extragonadal seminoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Extragonadal Seminoma", "shortest_name_length": 31}
{"curie": "MONDO:0005620", "names": ["HCHWA", "CAA, familial", "angiopathy congophilic", "Congophilic Angiopathy", "congophilic angiopathy", "Congophilic angiopathy", "Angiopathy, Congophilic", "Congophilic Angiopathies", "cerebral amyloid angiopathy", "Cerebral Amyloid Angiopathy", "Cerebral amyloid angiopathy", "Angiopathy, Cerebral Amyloid", "Amyloid Angiopathy, Cerebral", "Cerebral Amyloid Angiopathies", "CAA - Cerebral amyloid angiopathy", "Familial Cerebral Amyloid Angiopathy", "Familial cerebral amyloid angiopathy", "Cerebral Amyloid Angiopathy, Genetic", "cerebral amyloid angiopathy, genetic", "Cerebral Amyloid Angiopathy, Familial", "cerebral amyloid angiopathy, familial", "Cerebral amyloid angiopathy (disorder)", "cerebral amyloid angiopathy (diagnosis)", "Familial cerebral hemorrhage, amyloid type", "Familial cerebral haemorrhage, amyloid type", "dutch hereditary cerebral amyloid angiopathy", "Autosomal Dominant Cerebrovascular Amyloidosis", "Hereditary Cerebral Hemorrhage with Amyloidosis", "Cerebral Hemorrhage, Hereditary, with Amyloidosis", "hereditary cerebral haemorrhage with amyloidosis - Dutch type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral amyloid angiopathy", "shortest_name_length": 5}
{"curie": "MONDO:0020635", "names": ["Meningioma malignant", "Malignant meningioma", "MALIGNANT MENINGIOMA", "Malignant Meningioma", "malignant meningioma", "meningioma, malignant", "Meningioma, malignant", "Malignant Meningiomas", "Anaplastic Meningioma", "Anaplastic meningioma", "Meningiomas malignant", "Meningioma, Malignant", "anaplastic meningioma", "Meningioma, anaplastic", "Meningiomas, Malignant", "Meningioma malignant NOS", "malignant meningioma (diagnosis)", "Anaplastic (Malignant) Meningioma", "meningioma, anaplastic, malignant", "anaplastic (malignant) meningioma", "Meningioma, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anaplastic meningioma", "shortest_name_length": 20}
{"curie": "MONDO:0002908", "names": ["Glucose Metabolic Disorder", "glucose metabolism disease", "Disorder, Glucose Metabolic", "Glucose Metabolism Disorder", "Metabolic Disorder, Glucose", "glucose metabolism disorder", "metabolic glucose disorders", "Glucose Metabolic Disorders", "Metabolic Disorders, Glucose", "Disorders, Glucose Metabolic", "Glucose Metabolism Disorders", "Metabolism Disorder, Glucose", "disorders glucose metabolism", "Disorder, Glucose Metabolism", "glucose metabolism disorders", "Disorders, Glucose Metabolism", "Metabolism Disorders, Glucose", "disorder of glucose metabolism", "Disorder of glucose metabolism", "Disorder of Glucose Metabolism", "disorders of glucose metabolism", "Disorder of glucose metabolism (disorder)", "disorders of glucose metabolism (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glucose metabolism disease", "shortest_name_length": 26}
{"curie": "MONDO:0015744", "names": ["Trisomy 19qter", "trisomy 19qter", "distal trisomy 19q", "Distal trisomy 19q", "Distal duplication 19q", "distal duplication 19q", "distal trisomy type 19q", "telomeric duplication 19q", "Telomeric duplication 19q", "Distal trisomy 19q syndrome", "Distal trisomy 19q syndrome (disorder)", "Distal trisomy 19q syndrome (diagnosis)", "anomaly of chromosome pair 19q partial trisomy syndrome distal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal trisomy 19q", "shortest_name_length": 14}
{"curie": "MONDO:0011355", "names": ["CORD7", "CONE-ROD DYSTROPHY 7", "cone-rod dystrophy 7", "Cone-Rod Dystrophy 7", "RIMS1 cone-rod dystrophy", "cone-rod dystrophy type 7", "cone-rod dystrophy caused by mutation in RIMS1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cone-rod dystrophy 7", "shortest_name_length": 5}
{"curie": "UMLS:C1333841", "names": ["Grade 3 Clear Cell Renal Cell Carcinoma", "Grade 3 Conventional (Clear Cell) Renal Cell Carcinoma", "G3 Nuclei very irregular, approximately 20 um; nucleoli large and prominent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade 3 Clear Cell Renal Cell Carcinoma", "shortest_name_length": 39}
{"curie": "UMLS:C0751554", "names": ["Motor Tic Disorder", "Motor tic disorder", "Motor Tic Disorders", "Tic Disorder, Motor", "Tic Disorders, Motor", "Motor tic disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Motor Tic Disorders", "shortest_name_length": 18}
{"curie": "MONDO:0004393", "names": ["Mixed Astrocytoma-Ependymoma", "mixed astrocytoma-ependymoma", "Mixed astrocytoma-ependymoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed astrocytoma-ependymoma", "shortest_name_length": 28}
{"curie": "UMLS:C4683015", "names": ["Stage IIA Eyelid Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Eyelid Carcinoma AJCC v8", "shortest_name_length": 34}
{"curie": "MONDO:0004640", "names": ["Gastritis;alcohol", "alcohol; gastritis", "GASTRITIS ALCOHOLIC", "Gastritis alcoholic", "alcoholic gastritis", "Alcoholic gastritis", "Alcoholic Gastritis", "gastritis; alcoholic", "Alcoholic gastritis (disorder)", "alcoholic gastritis (diagnosis)", "Alcoholic gastritis, with hemorrhage", "alcoholic gastritis, with hemorrhage", "Alcoholic gastritis, without mention of hemorrhage", "alcoholic gastritis, without mention of hemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alcoholic gastritis", "shortest_name_length": 17}
{"curie": "MONDO:0011105", "names": ["alacrima, congenital, autosomal recessive", "ALACRIMA, CONGENITAL, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alacrima, congenital, autosomal recessive", "shortest_name_length": 41}
{"curie": "MONDO:0000545", "names": ["sublingual gland adenoid cystic carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sublingual gland adenoid cystic carcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0014527", "names": ["RJALS", "RUIJS-Aalfs syndrome", "RUIJS-AALFS SYNDROME", "Ruijs-Aalfs syndrome", "Ruijs Aalfs syndrome", "Progeroid features-hepatocellular carcinoma predisposition syndrome", "progeroid features-hepatocellular carcinoma predisposition syndrome", "Progeroid features, hepatocellular carcinoma predisposition syndrome", "Progeroid features, hepatocellular carcinoma predisposition syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progeroid features-hepatocellular carcinoma predisposition syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0006121", "names": ["CFT", "Calcifying fibrous tumor", "calcifying fibrous tumor", "Calcifying Fibrous Tumor", "Calcifying fibrous tumour", "Calcifying fibrous pseudotumor", "calcifying fibrous pseudotumor", "Calcifying Fibrous Pseudotumor", "Calcifying fibrous pseudotumour", "Calcifying fibrous tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "calcifying fibrous tumor", "shortest_name_length": 3}
{"curie": "UMLS:C0400823", "names": ["neutropenic colitis", "Neutropenic colitis", "colitis neutropenic", "Neutropenic colitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neutropenic colitis", "shortest_name_length": 19}
{"curie": "MONDO:0021530", "names": ["Benign Subglottic Tumor", "benign subglottic tumor", "Benign Subglottis Tumor", "benign subglottis tumor", "benign subglottic neoplasm", "Benign Tumor of Subglottis", "Benign Subglottis Neoplasm", "benign subglottis neoplasm", "Benign tumor of subglottis", "benign tumor of subglottis", "Benign Subglottic Neoplasm", "subglottis benign neoplasm", "Benign tumour of subglottis", "benign neoplasm of subglottis", "Benign Neoplasm of Subglottis", "Benign neoplasm of subglottis", "benign tumor of the subglottis", "Benign Tumor of the Subglottis", "benign neoplasm of the subglottis", "Benign Neoplasm of the Subglottis", "Benign neoplasm of subglottis (disorder)", "benign neoplasm of subglottis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of subglottis", "shortest_name_length": 23}
{"curie": "MONDO:0007445", "names": ["DPR", "Dermatopathia pigmentosa reticularis", "dermatopathia pigmentosa reticularis", "DERMATOPATHIA PIGMENTOSA RETICULARIS", "DPR - Dermatopathia pigmentosa reticularis", "Dermatopathia pigmentosa reticularis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermatopathia pigmentosa reticularis", "shortest_name_length": 3}
{"curie": "MONDO:0024526", "names": ["ZLS1", "Laband syndrome", "ZIMMERMANN-LABAND SYNDROME 1", "Zimmermann-Laband syndrome 1", "KCNH1 Zimmermann-Laband syndrome", "Zimmermann-Laband syndrome caused by mutation in KCNH1", "fibromatosis, gingival, with abnormal fingers, fingernails, Nose, and ears, and splenomegaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Zimmermann-Laband syndrome 1", "shortest_name_length": 4}
{"curie": "UMLS:C1561701", "names": ["Behavioral sleep problem", "Behavioural sleep problem", "Behavioral insomnia of childhood", "Behavioral Insomnia of Childhood", "behavioral insomnia of childhood", "Behavioural insomnia of childhood", "Behavioral insomnia of childhood (disorder)", "behavioral insomnia of childhood (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Behavioral insomnia of childhood", "shortest_name_length": 24}
{"curie": "UMLS:C5557215", "names": ["Epiglottic Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epiglottic Squamous Cell Carcinoma", "shortest_name_length": 34}
{"curie": "UMLS:C0751635", "names": ["Common Carotid Artery Stenosis", "Stenosis, Common Carotid Artery"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Common Carotid Artery Stenosis", "shortest_name_length": 30}
{"curie": "MONDO:0042433", "names": ["fungal endocarditis", "Fungal endocarditis", "mycotic endocarditis", "Mycotic endocarditis", "endocarditis; mycotic", "endocarditis; mycosis", "mycotic; endocarditis", "mycosis; endocarditis", "Endocarditis fungal NOS", "Fungal endocarditis, NOS", "Mycotic endocarditis, NOS", "acute fungal endocarditis", "Fungi endocarditis (disease)", "Mycotic endocarditis (disorder)", "Fungi caused endocarditis (disease)", "acute fungal endocarditis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mycotic endocarditis", "shortest_name_length": 19}
{"curie": "MONDO:0012629", "names": ["DYT20", "PNKD2", "Dystonia 20", "dystonia 20", "DYSTONIA 20", "PAROXYSMAL NONKINESIGENIC DYSKINESIA 2", "Paroxysmal Nonkinesigenic Dyskinesia 2", "paroxysmal nonkinesigenic dyskinesia 2", "paroxysmal nonkinesigenic dyskinesia type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paroxysmal nonkinesigenic dyskinesia 2", "shortest_name_length": 5}
{"curie": "UMLS:C1881586", "names": ["Malignant Pancreatic Vipoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Pancreatic Vipoma", "shortest_name_length": 27}
{"curie": "MONDO:0015663", "names": ["Russell syndrome", "diencephalic syndrome", "Diencephalic Syndrome", "diencephalic cachexia", "Diencephalic syndrome", "Diencephalic cachexia", "Russell diencephalic cachexia", "Diencephalic syndrome (disorder)", "Diencephalic syndrome of infancy", "Diencephalic Syndrome of Infancy", "diencephalic syndrome of infancy", "Diencephalic syndrome of childhood", "diencephalic syndrome of childhood", "diencephalic syndrome of emaciation", "Diencephalic syndrome of emaciation", "Diencephalic syndrome of infancy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diencephalic syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0009142", "names": ["DYSTONIA WITH RINGBINDEN", "dystonia with Ringbinden", "Dystonia with Ringbinden"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dystonia with Ringbinden", "shortest_name_length": 24}
{"curie": "MONDO:0011635", "names": ["MNG3", "GOITER, MULTINODULAR 3", "goiter, multinodular 3", "Goiter, Multinodular 3", "goiter, multinodular, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "goiter, multinodular 3", "shortest_name_length": 4}
{"curie": "MONDO:0030639", "names": ["Teebi hypertelorism syndrome", "Brachycephalofrontonasal dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Teebi hypertelorism syndrome", "shortest_name_length": 28}
{"curie": "UMLS:C0752299", "names": ["Sleep-Wake Transition Disorder", "Transition Disorder, Sleep-Wake", "Sleep Wake Transition Disorders", "Sleep-Wake Transition Disorders", "Transition Disorders, Sleep-Wake", "Sleep-Wake Transitional Disorder", "Transition Disorders, Sleep Wake", "Sleep Wake Transitional Disorders", "Transitional Disorder, Sleep-Wake", "Sleep-Wake Transitional Disorders", "Transitional Disorders, Sleep Wake", "Transitional Disorders, Sleep-Wake"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sleep Wake Transition Disorders", "shortest_name_length": 30}
{"curie": "MONDO:0700177", "names": ["Feline Mammary Carcinoma", "feline mammary carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "feline mammary carcinoma", "shortest_name_length": 24}
{"curie": "MONDO:0013078", "names": ["T1D24", "IDDM24", "TYPE 1 DIABETES MELLITUS 24", "type 1 diabetes mellitus 24", "insulin-dependent diabetes mellitus 24", "Insulin-Dependent Diabetes Mellitus 24", "Diabetes Mellitus, Insulin-Dependent, 24", "DIABETES MELLITUS, INSULIN-DEPENDENT, 24", "diabetes mellitus, insulin-dependent, 24"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type 1 diabetes mellitus 24", "shortest_name_length": 5}
{"curie": "MONDO:0010910", "names": ["ENUR1", "Bedwetting", "enuresis, nocturnal, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "enuresis, nocturnal, 1", "shortest_name_length": 5}
{"curie": "MONDO:0009235", "names": ["FRFB", "familial benign fleck retina", "fleck retina, familial benign", "Fleck Retina, Familial Benign", "FLECK RETINA, FAMILIAL BENIGN", "FLECK retina, familial benign", "familial benign flecked retina", "Familial benign flecked retina", "Familial benign flecked retina (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial benign flecked retina", "shortest_name_length": 4}
{"curie": "UMLS:C0086367", "names": ["ROS", "Savage Syndrome", "Resistant Ovary Syndrome", "Resistant ovary syndrome", "ovary; resistant syndrome", "resistant ovary; syndrome", "syndrome; resistant ovary", "ovary; syndrome, resistant", "syndrome; ovary, resistant", "Resistant ovary syndrome (disorder)", "Gonadotropin-Resistant Ovary Syndrome", "Gonadotropin Resistant Ovary Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gonadotropin-Resistant Ovary Syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0013057", "names": ["PSORS12", "psoriasis 12", "psoriasis susceptibility 12", "PSORIASIS 12, SUSCEPTIBILITY TO", "psoriasis 12, susceptibility to", "PSORIASIS SUSCEPTIBILITY 12 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "psoriasis 12, susceptibility to", "shortest_name_length": 7}
{"curie": "MONDO:0016130", "names": ["Fungal myositis", "fungal myositis", "Fungal myositis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fungal myositis", "shortest_name_length": 15}
{"curie": "UMLS:C0040524", "names": ["toxemia", "Toxemia", "TOXEMIA", "Toxemias", "Toxaemia", "toxemias", "toxaemia", "Toxemia, NOS", "Toxaemia, NOS", "Septic Toxemia", "septic; toxemia", "blood poisoning", "toxemia; septic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Septic Toxemia", "shortest_name_length": 7}
{"curie": "UMLS:C2981372", "names": ["Stage IIIA Esophageal Adenocarcinoma", "Stage IIIA Esophageal Adenocarcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Esophageal Adenocarcinoma AJCC v7", "shortest_name_length": 36}
{"curie": "MONDO:0019372", "names": ["SBC", "Bone cyst", "Bone Cyst", "bone cyst", "BONE CYST", "Bone cysts", "bone; cyst", "Cyst, Bone", "Bone Cysts", "cyst; bone", "bone cysts", "Cysts, Bone", "cyst of bone", "Cyst of bone", "Solitary Cyst", "Bone cyst NOS", "solitary cyst", "Solitary Cysts", "Cyst, Solitary", "Cysts, Solitary", "Simple bone cyst", "simple bone cyst", "Simple Bone Cyst", "cyst of the bone", "Local cyst of bone", "Solitary bone cyst", "Solitary Bone Cyst", "solitary bone cyst", "bone; solitary cyst", "solitary; cyst bone", "bone; cyst, solitary", "cyst; solitary, bone", "Bone cyst (disorder)", "cyst; bone, solitary", "Unicameral Bone Cyst", "Unicameral bone cyst", "unicameral bone cyst", "Hemorrhagic Bone Cyst", "bone cyst (diagnosis)", "Local cyst of bone, NOS", "Cyst of bone, unspecified", "Solitary bone cyst (disorder)", "solitary bone cyst (diagnosis)", "Localized cyst of bone, unspecified", "Bone cyst (morphologic abnormality)", "Solitary bone cyst, unspecified site", "Solitary bone cyst, site unspecified", "Cyst of bone (localized), unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "solitary bone cyst", "shortest_name_length": 3}
{"curie": "MONDO:0023167", "names": ["focal alopecia congenital megalencephaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal alopecia congenital megalencephaly", "shortest_name_length": 40}
{"curie": "MONDO:0032744", "names": ["SPGF37", "SPERMATOGENIC FAILURE 37", "spermatogenic failure 37"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 37", "shortest_name_length": 6}
{"curie": "MONDO:0003471", "names": ["nits", "Nits", "head lice", "Head lice", "head louse", "Head louse", "Lousy hair", "HEAD SKIN LICE", "lice; head lice", "Nits - head lice", "Head pediculosis", "Pediculus capitis", "Nit infested hair", "pediculus capitis", "Lice infested hair", "Pediculosis capitis", "pediculosis capitis", "PEDICULOSIS CAPITIS", "Head lice infestation", "head lice infestation", "Head louse infestation", "Head-louse infestation", "head louse infestation", "Infestation (by);lice;head", "head lice (physical finding)", "Pediculus capitis infestation", "Pediculus capitis - head lice", "Pediculosis capitis (disorder)", "Pediculus capitis [head louse]", "Pediculus capitis (head louse)", "pediculosis capitis (diagnosis)", "Pediculus humanus capitis infection", "Pediculus humanus capitis infestation", "infections, Pediculus humanus capitis", "Pediculus humanus capitis; pediculosis", "pediculosis; Pediculus humanus capitis", "Pediculosis due to Pediculus humanus capitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pediculus humanus capitis infestation", "shortest_name_length": 4}
{"curie": "MONDO:0011440", "names": ["Hyt2", "HYT2", "HYPERTENSION, ESSENTIAL, SUSCEPTIBILITY TO, 2", "hypertension, essential, susceptibility to, 2", "hypertension, essential, susceptibility to, type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertension, essential, susceptibility to, 2", "shortest_name_length": 4}
{"curie": "MONDO:0019718", "names": ["lethal chondrodysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal chondrodysplasia", "shortest_name_length": 23}
{"curie": "MONDO:0016479", "names": ["Silver-Russell syndrome due to dup(7)(p11.2p13)", "Silver-Russell syndrome due to trisomy 7p11.2p13", "Silver-Russell syndrome due to trisomy 7p11.2-p13", "silver-Russell syndrome due to 7p11.2p13 microduplication", "Silver-Russell syndrome due to 7p11.2-p13 microduplication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "silver-Russell syndrome due to 7p11.2p13 microduplication", "shortest_name_length": 47}
{"curie": "MONDO:0016002", "names": ["kEDS", "EDS6", "EDS 6", "EDS VI", "EDS VIA", "EDSKSCL1", "kEDS-PLOD1", "Nevo syndrome", "NEVO SYNDROME", "nevo syndrome", "EDS6A, formerly", "EDS6A, FORMERLY", "EDS 6 (formerly)", "Kyphoscoliotic EDS", "kyphoscoliotic EDS", "Cutis hyperelastica", "Ocular-scoliotic EDS", "EDS, oculoscoliotic type", "EDS, kyphoscoliotic type", "Cerebral gigantism nevo type", "Ehlers-Danlos syndrome type 6", "Ehlers-Danlos syndrome type VI", "Ehlers-Danlos syndrome type 6A", "Ehlers-Danlos syndrome, type 6", "type VI Ehlers-Danlos syndrome", "EHLERS-DANLOS SYNDROME, TYPE VI", "Ehlers-Danlos Syndrome, Type VI", "Ehlers-Danlos syndrome, type VI", "Lysyl hydroxylase-deficient EDS", "Ehlers-Danlos Syndrome, Type VIA", "Ehlers-Danlos syndrome, type Via", "Ehlers-Danlos syndrome, type VIA", "Ehlers-Danlos syndrome, type 6 A", "kyphoscoliotic Ehlers-Danlos syndrome", "Kyphoscoliotic Ehlers-Danlos syndrome", "Hydroxylysine-deficient collagen disease", "Ehlers-Danlos syndrome type 6 (formerly)", "Ehlers-Danlos syndrome type 6A (formerly)", "Ehlers-Danlos syndrome kyphoscoliotic type", "Ehlers-Danlos syndrome, type Via, formerly", "EHLERS-DANLOS SYNDROME, TYPE VIA, FORMERLY", "Protocollagen lysyl hydroxylase deficiency", "Ehlers-Danlos syndrome, type VIA, formerly", "Ehlers-Danlos syndrome oculoscoliotic type", "Ehlers-Danlos syndrome, oculoscoliotic type", "Ehlers-Danlos syndrome, type VI (diagnosis)", "Ehlers-Danlos syndrome, kyphoscoliotic type", "Ehlers-Danlos syndrome, kyphoscoliosis type", "Ehlers-Danlos syndrome kyphoscoliotic type 1", "Ehlers-Danlos syndrome, kyphoscoliotic type 1", "EHLERS-DANLOS SYNDROME, OCULAR-SCOLIOTIC TYPE", "Ocular scoliotic EDS (Ehlers-Danlos syndrome)", "Ehlers-Danlos syndrome, ocular-scoliotic type", "Ehlers-Danlos syndrome, kyphoscoliotic type, 1", "EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 1", "Ehlers-Danlos syndrome, hydroxylysine-deficient", "Ehlers-Danlos syndrome, lysyl hydroxylase deficient", "Ehlers-Danlos syndrome kyphoscoliotic type (disorder)", "Kyphoscoliotic EDS due to lysyl hydroxylase 1 deficiency", "Ehlers-Danlos syndrome, hydroxylysine-deficient (disorder)", "kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency", "Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ehlers-Danlos syndrome, kyphoscoliotic type 1", "shortest_name_length": 4}
{"curie": "UMLS:C0243065", "names": ["Aplasia", "aplasia", "Aplasias", "APLASIAS", "Aplasia NOS", "Aplasia, NOS", "Aplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aplasia, NOS", "shortest_name_length": 7}
{"curie": "MONDO:0021412", "names": ["antral polyp", "Antral polyp", "maxillary sinus polyp", "Maxillary Sinus Polyp", "Maxillary sinus polyp", "maxillary polyps sinus", "Maxillary Antral Polyp", "maxillary antral polyp", "polyp of maxillary sinus", "Antral (maxillary) polyp", "Polyp of Maxillary Sinus", "Maxillary polyp of sinus", "Polyp of maxillary sinus", "Polyp of sinus, maxillary", "Polyp of the Maxillary Sinus", "polyp of the maxillary sinus", "Antral polyp (of maxillary sinus)", "Polyp of maxillary sinus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyp of maxillary sinus", "shortest_name_length": 12}
{"curie": "UMLS:C0334494", "names": ["Borderline Brenner tumor", "Borderline Brenner tumour", "Proliferating Brenner Tumor", "Proliferating Brenner tumor", "proliferating; Brenner tumor", "Proliferating Brenner tumour", "Brenner tumor, proliferating", "Brenner tumour, proliferating", "tumor; Brenner, proliferating", "Brenner; tumor, proliferating", "Borderline Ovarian Brenner Tumor", "Borderline Brenner Tumor of Ovary", "Borderline Ovarian Brenner Neoplasm", "Proliferating Ovarian Brenner Tumor", "Proliferating Brenner Tumor of Ovary", "Brenner tumor, borderline malignancy", "borderline malignancy; Brenner tumor", "Borderline Brenner Neoplasm of Ovary", "Brenner tumor, atypical proliferative", "Brenner; tumor, borderline malignancy", "Brenner tumor - borderline malignancy", "Brenner tumour, borderline malignancy", "Borderline Brenner Tumor of the Ovary", "tumor; Brenner, borderline malignancy", "Brenner tumour - borderline malignancy", "Proliferating Ovarian Brenner Neoplasm", "Brenner tumour, atypical proliferative", "Proliferating Brenner Neoplasm of Ovary", "Proliferating Brenner Tumor of the Ovary", "Borderline Brenner Neoplasm of the Ovary", "Borderline Ovarian Transitional Cell Tumor", "Proliferating Brenner Neoplasm of the Ovary", "Borderline Ovarian Transitional Cell Neoplasm", "Low Malignancy Potential Ovarian Brenner Tumor", "Low Malignancy Potential Brenner Tumor of Ovary", "Low Malignancy Potential Ovarian Brenner Neoplasm", "Low Malignancy Potential Brenner Neoplasm of Ovary", "Low Malignancy Potential Brenner Tumor of the Ovary", "Low Malignancy Potential Brenner Neoplasm of the Ovary", "Brenner tumor, borderline malignancy (morphologic abnormality)", "Borderline Ovarian Brenner Tumor/Atypical Proliferative Ovarian Brenner Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Proliferating Brenner Tumor", "shortest_name_length": 24}
{"curie": "UMLS:C1882293", "names": ["PAROXYSMAL AV BLOCK", "Paroxysmal AV block", "Paroxysmal AV Block", "Paroxysmal Atrioventricular Block", "Paroxysmal atrioventricular block", "Paroxysmal Atrioventricular Block by ECG Finding", "Paroxysmal Atrioventricular Block by EKG Finding"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paroxysmal atrioventricular block", "shortest_name_length": 19}
{"curie": "MONDO:0054750", "names": ["ALS24", "AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 24", "amyotrophic lateral sclerosis, susceptibility to, 24"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyotrophic lateral sclerosis, susceptibility to, 24", "shortest_name_length": 5}
{"curie": "UMLS:C1696495", "names": ["Infusion site vesicles", "Infusion site blisters"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infusion site vesicles", "shortest_name_length": 22}
{"curie": "MONDO:0018570", "names": ["HPP", "HPPC", "Rathbun disease", "hypophosphatasia", "HYPOPHOSPHATASIA", "Rathburn disease", "Hypophosphatasia", "Hypophosphatasias", "hypophosphatasia mild", "Hypophosphatasia, NOS", "Phosphoethanolaminuria", "phosphoethanolaminuria", "phosphoethanol-aminuria", "Juvenile hypophosphatasia", "childhood hypophosphatasia", "hypophospatasia, childhood", "Childhood hypophosphatasia", "Hypophosphatasia (disorder)", "Hypophosphatasia, Childhood", "HYPOPHOSPHATASIA, CHILDHOOD", "hypophosphatasia (diagnosis)", "Childhood-onset Rathbun disease", "Alkaline phosphatase deficiency", "Hypophosphatasia, childhood type", "Childhood-onset hypophosphatasia", "Deficiency of alkaline phosphatase", "deficiency of alkaline phosphatase", "Childhood hypophosphatasia (disorder)", "Childhood-onset phosphoethanolaminuria", "Deficiency of alkaline phosphatase (disorder)", "deficiency of alkaline phosphatase (diagnosis)", "deficiency of alkaline phosphatase (disorder) [ambiguous]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypophosphatasia", "shortest_name_length": 3}
{"curie": "MONDO:0017916", "names": ["pure or complex X-linked spastic paraplegia", "Pure or complicated X-linked spastic paraplegia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pure or complex X-linked spastic paraplegia", "shortest_name_length": 43}
{"curie": "MONDO:0008414", "names": ["SCZD1", "SCHIZOPHRENIA 1", "schizophrenia 1", "SCHIZOPHRENIA 1 WITH OR WITHOUT AN AFFECTIVE DISORDER", "schizophrenia 1 with or without an affective disorder", "SCHIZOPHRENIA SUSCEPTIBILITY LOCUS, CHROMOSOME 5-RELATED", "schizophrenia susceptibility locus, chromosome 5-related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schizophrenia 1", "shortest_name_length": 5}
{"curie": "MONDO:0010531", "names": ["Ladda Zonana Ramer syndrome", "Ladda-Zonana-Ramer syndrome", "Contractures ectodermal dysplasia cleft lip palate", "contractures ectodermal dysplasia cleft lip palate", "contractures-ectodermal dysplasia-cleft lip/palate syndrome", "Contractures-ectodermal dysplasia-cleft lip/palate syndrome", "Contracture with ectodermal dysplasia and orofacial cleft syndrome", "contracture with ectodermal dysplasia and orofacial cleft syndrome", "Contracture with ectodermal dysplasia and orofacial cleft syndrome (disorder)", "Arthrogryposis, ectodermal dysplasia, cleft lip palate and developmental delay", "contracture with ectodermal dysplasia and orofacial cleft syndrome (diagnosis)", "arthrogryposis, ectodermal dysplasia, cleft LIP/palate, and developmental delay", "ARTHROGRYPOSIS, ECTODERMAL DYSPLASIA, CLEFT LIP/PALATE, AND DEVELOPMENTAL DELAY", "Arthrogryposis, ectodermal dysplasia, cleft lip-palate, and developmental delay", "Congenital contractures, ectodermal dysplasia, cleft lip-palate, and developmental impairment", "congenital contractures, ectodermal dysplasia, cleft lip/palate, and developmental impairment"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "contractures-ectodermal dysplasia-cleft lip/palate syndrome", "shortest_name_length": 27}
{"curie": "MONDO:0008727", "names": ["HSDB", "HSDB3", "HSD3B deficiency", "3beta-Hsd Deficiency", "3 beta-HSD deficiency", "3-BETA-HSD DEFICIENCY", "3 Beta-Hsd Deficiency", "3-Beta-HSD deficiency", "3-beta HSD deficiency", "Adrenal hyperplasia 2", "adrenal hyperplasia 2", "3-beta HSD Deficiency", "ADRENAL HYPERPLASIA II", "adrenal hyperplasia II", "3 alpha beta-HSD deficiency", "3 beta-ol Dehydrogenase Deficiency", "CAH - 3 beta-dehydrogenase deficiency", "Congenital adrenal hyperplasia, type 4", "3b-Hydroxysteroid Dehydrogenase Deficiency", "3b-hydroxysteroid dehydrogenase deficiency", "3beta-Hydroxysteroid Dehydrogenase Deficiency", "3-Beta-hydroxysteroid dehydrogenase deficiency", "3-Beta Hydroxysteroid Dehydrogenase Deficiency", "3-Beta-Hydroxysteroid Dehydrogenase Deficiency", "3 beta-hydroxysteroid dehydrogenase deficiency", "3 beta-Hydroxysteroid dehydrogenase deficiency", "3-beta hydroxysteroid dehydrogenase; deficiency", "3beta-Hsd Deficiency Congenital Adrenal Hyperplasia", "3 alpha beta-hydroxysteroid dehydrogenase deficiency", "Type II 3beta-Hydroxysteroid Dehydrogenase Deficiency", "type II 3-beta-hydroxysteroid dehydrogenase deficiency", "CAH due to 3-beta-hydroxysteroid dehydrogenase deficiency", "3 beta-Hydroxysteroid dehydrogenase deficiency (disorder)", "3 beta-hydroxysteroid dehydrogenase deficiency (diagnosis)", "3-BETA-hydroxysteroid dehydrogenase, type II, deficiency OF", "3 alpha beta-hydroxysteroid dehydrogenase, type 2, deficiency of", "Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency", "congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency", "adrenal hyperplasia, congenital, due to 3-Beta-hydroxysteroid dehydrogenase 2 deficiency", "adrenal hyperplasia, congenital, due to 3-BETA-hydroxysteroid dehydrogenase 2 deficiency", "ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 3-BETA-HYDROXYSTEROID DEHYDROGENASE 2 DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0021159", "names": ["salpingitis gonococcal", "gonococcal salpingitis", "Salpingitis gonococcal", "Gonococcal salpingitis", "Salpingitis gonococcal NOS", "Gonococcal salpingitis (disorder)", "Neisseria gonorrhoeae salpingitis", "Gonococcal salpingitis (diagnosis)", "Neisseria gonorrhoeae caused salpingitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gonococcal salpingitis", "shortest_name_length": 22}
{"curie": "MONDO:0004577", "names": ["cornea ulcer", "ulcer cornea", "Corneal Ulcer", "Corneal ulcer", "cornea; ulcer", "Ulcer corneal", "ulcer; cornea", "CORNEAL ULCER", "corneal ulcer", "ULCER CORNEAL", "Ulcer;corneal", "cornea ulcers", "Corneal ulcers", "corneal ulcers", "Ulcer, corneal", "Cornea--Ulcers", "Ulcer, Corneal", "erosion; cornea", "CORNEAL ULCERATION", "Corneal ulceration", "corneal ulceration", "Corneal ulcer, NOS", "Corneal ulcerations", "Ulcerative Keratitis", "ulcerative keratitis", "cornea ulcer disease", "Keratitis, Ulcerative", "Ulcerative Keratitides", "Keratitides, Ulcerative", "ulcer disease of cornea", "Corneal ulcer (disorder)", "corneal ulcer (diagnosis)", "Unspecified corneal ulcer", "Corneal ulcer, unspecified", "Corneal ulcer (including herpetic)", "corneal ulceration (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal ulcer", "shortest_name_length": 12}
{"curie": "UMLS:C0751506", "names": ["rem sleep deprivation", "REM Sleep Deprivation", "Sleep Deprivation, REM", "Deprivation, REM Sleep"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "REM Sleep Deprivation", "shortest_name_length": 21}
{"curie": "MONDO:0100438", "names": ["LCA4", "AIPL1 retinopathy", "cone-rod dystrophy", "AIPL1-related retinopathy", "Leber congenital amaurosis 4", "retinitis pigmentosa, juvenile", "AIPL1 Leber congenital amaurosis", "Leber congenital amaurosis type 4", "cone-rod dystrophy, AIPL1-related", "amaurosis congenita of Leber, type 4", "retinitis pigmentosa, juvenile, AIPL1-related", "Leber congenital amaurosis caused by mutation in AIPL1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIPL1-related retinopathy", "shortest_name_length": 4}
{"curie": "UMLS:C5237355", "names": ["CIC-DUX4L Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CIC-DUX4L Sarcoma", "shortest_name_length": 17}
{"curie": "MONDO:0009863", "names": ["PTSD", "PTPSD", "HPABH4A", "PTS Deficiency", "PTS DEFICIENCY", "PTS deficiency", "PTPS deficiency", "Phenylketonuria III", "BH4-deficient hyperphenylalaninemia A", "hyperphenylalanemia, BH4-deficient, A", "Hyperphenylalaninemia, BH4-deficient A", "hyperphenylalaninemia, BH4-deficient A", "HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A", "hyperphenylalaninemia, BH4-deficient, A", "Bh4-deficient hyperphenylalaninemia type A", "Hyperphenylalaninemia, BH4-Deficient, Type A", "hyperphenylalaninemia, BH4-deficient, type A", "hyperphenylalaninemia, Bh4-deficient, type a", "6-pyruvoyl tetrahydropterin synthase deficiency", "6-PYRUVOYL-TETRAHYDROPTERIN SYNTHASE DEFICIENCY", "6-Pyruvoyl-tetrahydropterin synthase deficiency", "6-pyruvoyl-tetrahydropterin synthase deficiency", "6-pyruvoyl Tetrahydropterin Synthase Deficiency", "6-Pyruvoyl tetrahydropterin synthase deficiency", "6-Pyruvoyl-tetrahydrobiopterin synthase deficiency", "6PTS - 6-Pyruvoyl-tetrahydrobiopterin synthase deficiency", "6-Pyruvoyl-tetrahydrobiopterin synthase deficiency (disorder)", "HYPERPHENYLALANINEMIA, BH4-DEFICIENT, DUE TO PARTIAL PTS DEFICIENCY", "Hyperphenylalaninemia, BH4-Deficient, Due To Partial PTS Deficiency", "hyperphenylalaninemia, Bh4-deficient, due to partial PTS deficiency", "tetrahydobioperin-deficient hyperphenylalaninemia due to PTS deficiency", "hyperphenylalaninemia due to 6-pyruvoyltetrahydropterin synthase deficiency", "HYPERPHENYLALANINEMIA, TETRAHYDROBIOPTERIN-DEFICIENT, DUE TO PTS DEFICIENCY", "hyperphenylalaninemia, tetrahydrobiopterin-deficient, due to PTS deficiency", "Hyperphenylalaninemia, Tetrahydrobiopterin-Deficient, Due To PTS Deficiency", "Hyperphenylalaninemia due to 6-pyruvoyltetrahydropterin synthase deficiency", "hyperphenylalaninemia due to 6-pyruvoyl-tetrahydropterin synthase deficiency", "PTS deficiency hyperphenylalaninemia, BH4-deficient, due to partial PTS deficiency, included"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "BH4-deficient hyperphenylalaninemia A", "shortest_name_length": 4}
{"curie": "MONDO:0015280", "names": ["CFC", "CFC1", "CFCS", "CFC syndrome", "CFC Syndrome", "CFC SYNDROME", "cardiofaciocutaneous syndrome", "Cardiofaciocutaneous syndrome", "Cardiofaciocutaneous Syndrome", "Cardio-Facio-Cutaneous Syndrome", "Cardio-facio-cutaneous syndrome", "cardio-facio-cutaneous syndrome", "CARDIOFACIOCUTANEOUS SYNDROME 1", "cardio-facial-cutaneous syndrome", "Cardiofaciocutaneous (CFC) Syndrome", "cardiofaciocutaneous (CFC) syndrome", "Cardio-facio-cutaneous syndrome (disorder)", "cardio-facio-cutaneous syndrome (diagnosis)", "congenital heart defects characteristic facial appearance ectodermal abnormalities and growth failure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiofaciocutaneous syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C0796439", "names": ["Stage IIC Adult Soft Tissue Sarcoma", "adult soft tissue sarcoma, stage IIC", "soft tissue sarcoma, adult, stage IIC", "sarcoma, adult soft tissue, stage IIC", "Stage IIC Adult Sarcoma of Soft Tissue", "Stage IIC Adult Sarcoma of the Soft Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIC Adult Soft Tissue Sarcoma", "shortest_name_length": 35}
{"curie": "MONDO:0043162", "names": ["pagon stephan syndrome", "Pagon Stephan syndrome", "Septo-optic dysplasia with digital anomalies", "septo-optic dysplasia with digital anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pagon stephan syndrome", "shortest_name_length": 22}
{"curie": "MONDO:0009296", "names": ["GLYCOPROTEIN STORAGE DISEASE", "Glycoprotein Storage Disease", "glycoprotein storage disease", "Glycoprotein storage disorder", "glycoprotein storage disorder", "Glycoprotein storage disorder, NOS", "Glycoprotein storage disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycoprotein storage disease", "shortest_name_length": 28}
{"curie": "MONDO:0005356", "names": ["coronary spasm", "CORONARY SPASM", "Coronary spasm", "coronary; spasm", "coronary spasms", "spasm; coronary", "coronaries spasm", "vasospasm coronary", "Coronary vasospasm", "coronary vasospasm", "Coronary Vasospasm", "a.coronaria; spasm", "Coronary Vasospasms", "coronary vasospasms", "Vasospasm, Coronary", "Spasm-induced angina", "coronary artery spasm", "Spasm coronary artery", "arteriospasm coronary", "CORONARY ARTERY SPASM", "SPASM CORONARY ARTERY", "Arteriospasm coronary", "Coronary Artery Spasm", "artery coronary spasm", "ARTERIOSPASM CORONARY", "Coronary artery spasm", "spasm-induced; angina", "spasm coronary artery", "Spasm;artery;coronary", "Spasm, Coronary Artery", "artery coronary spasms", "Artery Spasm, Coronary", "Coronary Artery Spasms", "spasm; coronary artery", "Coronary vascular spasm", "coronary artery vasospasm", "Coronary artery vasospasm", "Coronary Artery Vasospasm", "Vasospasm, Coronary Artery", "Artery Vasospasm, Coronary", "Coronary Artery Vasospasms", "Coronary artery spasm (disorder)", "coronary artery spasm (diagnosis)", "Angina pectoris with documented spasm", "angina pectoris; with documented spasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coronary vasospasm", "shortest_name_length": 14}
{"curie": "MONDO:0024302", "names": ["internal; leeches", "leeches; internal", "Internal hirudiniasis", "internal hirudiniasis", "Internal Hirudiniasis", "internal; hirudiniasis", "hirudiniasis; internal", "infestation; leeches, internal", "leeches; infestation, internal", "infestation; Hirudinea, internal", "Hirudinea; infestation, internal", "Internal hirudiniasis (disorder)", "internal hirudiniasis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "internal hirudiniasis", "shortest_name_length": 17}
{"curie": "UMLS:C4526975", "names": ["Stage I Small Intestinal, Esophageal, Colorectal, Mesenteric, and Peritoneal GIST AJCC v8", "Stage I Small Intestinal, Esophageal, Colorectal, Mesenteric, and Peritoneal Gastrointestinal Stromal Tumor (GIST)", "Stage I Small Intestinal, Esophageal, Colorectal, Mesenteric, and Peritoneal Gastrointestinal Stromal Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Small Intestinal, Esophageal, Colorectal, Mesenteric, and Peritoneal Gastrointestinal Stromal Tumor AJCC v8", "shortest_name_length": 89}
{"curie": "MONDO:0041752", "names": ["PB leprosy", "tuberculoid leprosy", "Borderline Tuberculoid", "paucibacillary leprosy", "Paucibacillary Leprosy", "Paucibacillary leprosy", "leprosy paucibacillary", "Borderline Tuberculoids", "Leprosy, Paucibacillary", "Tuberculoid, Borderline", "Tuberculoids, Borderline", "Paucibacillary Leprosies", "Indeterminate Tuberculoid", "Leprosies, Paucibacillary", "Tuberculoid, Indeterminate", "Indeterminate Tuberculoids", "Tuberculoids, Indeterminate", "Paucibacillary leprosy (disorder)", "Paucibacillary leprosy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paucibacillary leprosy", "shortest_name_length": 10}
{"curie": "UMLS:C1096225", "names": ["Vessel puncture site bleeding", "Vessel puncture site hemorrhage", "Vessel puncture site haemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vessel puncture site hemorrhage", "shortest_name_length": 29}
{"curie": "MONDO:0001276", "names": ["expressive; language", "disorder expressive language", "Expressive language disorder", "expressive language disorder", "Expressive Language Disorder", "disorders expressive language", "language disorder; expressive", "Expressive language impairment", "dysphasia; expressive, developmental", "expressive; dysphasia, developmental", "developmental; dysphasia, expressive", "expressive language learning disability", "Expressive language disorder (disorder)", "Expressive language disorder (diagnosis)", "Expressive language impairment (diagnosis)", "developmental expressive language disorder", "Developmental expressive language disorder", "language; developmental disorder, expressive", "developmental disorder; language, expressive", "Developmental expressive language disorder (disorder)", "developmental expressive language disorder (diagnosis)", "expressive language learning disability (physical finding)", "developmental disorder - speech articulation expressive language"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "expressive language disorder", "shortest_name_length": 20}
{"curie": "MONDO:0022410", "names": ["retinal ciliopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal ciliopathy", "shortest_name_length": 18}
{"curie": "UMLS:C1956415", "names": ["PND", "pnd", "pnds", "Cardiac Asthma", "cardiac asthma", "paroxysmal dyspnea", "dyspnea paroxysmal", "PAROXYSMAL NOCTURNAL DYSPNEA", "Dyspnea Paroxysmal Nocturnal", "dyspnea paroxysmal nocturnal", "DYSPNEA PAROXYSMAL NOCTURNAL", "Paroxysmal Nocturnal Dyspnea", "Paroxysmal nocturnal dyspnea", "Dyspnea paroxysmal nocturnal", "paroxysmal nocturnal dyspnea", "dyspnea nocturnal paroxysmal", "paroxysmal nocturnal dyspnoea", "dyspnoea paroxysmal nocturnal", "Dyspnea, Paroxysmal Nocturnal", "Paroxysmal nocturnal dyspnoea", "Dyspnea, paroxysmal nocturnal", "Dyspnoea paroxysmal nocturnal", "DYSPNEA, NOCTURNAL PAROXYSMAL", "Nocturnal Dyspnea, Paroxysmal", "paroxysmal nocturnal dyspnea pnd", "PND - Paroxysmal nocturnal dyspnea", "PND - Paroxysmal nocturnal dyspnoea", "Paroxysmal nocturnal dyspnea (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paroxysmal nocturnal dyspnea", "shortest_name_length": 3}
{"curie": "MONDO:0005082", "names": ["prad", "PRAD", "adenocarcinoma prostate", "prostate adenocarcinoma", "Prostate adenocarcinoma", "Prostate Adenocarcinoma", "PROSTATE, ADENOCARCINOMA", "prostatic adenocarcinoma", "adenocarcinoma prostatic", "adenocarcinoma, prostatic", "adenocarcinoma of prostate", "Adenocarcinoma of prostate", "Adenocarcinoma of Prostate", "prostate gland adenocarcinoma", "PROSTATE CANCER ADENOCARCINOMA", "prostate cancer adenocarcinoma", "Adenocarcinoma of the Prostate", "adenocarcinoma of the prostate", "prostate cancer, adenocarcinoma", "adenocarcinoma of prostate gland", "Adenocarcinoma of prostate (disorder)", "adenocarcinoma of prostate gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate adenocarcinoma", "shortest_name_length": 4}
{"curie": "UMLS:C4744754", "names": ["Thyroid Gland Schwannoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Schwannoma", "shortest_name_length": 24}
{"curie": "MONDO:0035235", "names": ["classic pyoderma gangrenosum", "Ulcerative pyoderma gangrenosum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "classic pyoderma gangrenosum", "shortest_name_length": 28}
{"curie": "MONDO:0002360", "names": ["Chondroma", "chondroma", "chondromas", "Chondromas", "Enchondroma", "enchondroma", "enchondromas", "Enchondromas", "Chondroma NOS", "Chondroma, NOS", "True chondroma", "CHONDROMA, BENIGN", "central chondroma", "chondroma, benign", "central Chondroma", "Central Chondroma", "Chondroma (morphologic abnormality)", "Enchondroma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chondroma", "shortest_name_length": 9}
{"curie": "MONDO:0011135", "names": ["SUPERIOR TRANSVERSE SCAPULAR LIGAMENT, CALCIFICATION OF, FAMILIAL", "Superior Transverse Scapular Ligament, Calcification Of, Familial", "superior transverse scapular ligament, calcification of, familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "superior transverse scapular ligament, calcification of, familial", "shortest_name_length": 65}
{"curie": "MONDO:0006452", "names": ["Thymic Carcinosarcoma", "thymic carcinosarcoma", "Thymus sarcomatoid carcinoma", "Thymic Sarcomatoid Carcinoma", "Thymus Sarcomatoid Carcinoma", "thymus sarcomatoid carcinoma", "thymic sarcomatoid carcinoma", "Thymic Spindle Cell Carcinoma", "thymic spindle cell carcinoma", "sarcomatoid carcinoma of Thymus", "Sarcomatoid Carcinoma of Thymus", "Sarcomatoid Carcinoma of the Thymus", "sarcomatoid carcinoma of the Thymus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thymic sarcomatoid carcinoma", "shortest_name_length": 21}
{"curie": "UMLS:C0267537", "names": ["cecity", "Cecity", "Cecitis", "cecitis", "caecitis", "Caecitis", "typhlitis", "Typhlitis", "Cecitis, NOS", "Typhlitis, NOS", "Cecum inflamed", "cecal inflammation", "Cecal inflammation", "Neutropenic Colitis", "Caecal inflammation", "cecitis (diagnosis)", "Typhlitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Typhlitis", "shortest_name_length": 6}
{"curie": "UMLS:C4288541", "names": ["Ovarian Seromucinous Adenofibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Seromucinous Adenofibroma", "shortest_name_length": 33}
{"curie": "UMLS:C0872054", "names": ["latent infection", "Latent Infection", "Infection, Latent", "Latent Infections", "infections latent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Latent Infection", "shortest_name_length": 16}
{"curie": "MONDO:0012302", "names": ["PFM3", "parietal foramina 3", "PARIETAL FORAMINA 3", "Parietal Foramina 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parietal foramina 3", "shortest_name_length": 4}
{"curie": "UMLS:C1336315", "names": ["Stage II Retinoblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Retinoblastoma", "shortest_name_length": 23}
{"curie": "MONDO:0012707", "names": ["FEB9", "familial febrile seizures 9", "febrile seizures, familial, 9", "FEBRILE SEIZURES, FAMILIAL, 9", "familial febrile convulsions 9", "FEBRILE CONVULSIONS, FAMILIAL, 9", "Febrile Convulsions, Familial, 9", "febrile convulsions, familial, 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial febrile seizures 9", "shortest_name_length": 4}
{"curie": "UMLS:C5419467", "names": ["Recurrent Malignant Lymphoid Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Malignant Lymphoid Neoplasm", "shortest_name_length": 37}
{"curie": "MONDO:0015943", "names": ["CSS", "EGPA", "CHURG STRAUSS", "churg strauss", "Churg-Strauss", "strauss churg", "Allergic Angiitis", "allergic angiitis", "Allergic angiitis", "ANGIITIS, ALLERGIC", "angiitis, allergic", "Angiitis, Allergic", "Allergic Angiitides", "allergic angiitides", "angiitides, allergic", "Angiitides, Allergic", "Churg-Strauss syndrome", "CHURG-STRAUSS SYNDROME", "Churg Strauss syndrome", "Churg Strauss Syndrome", "Churg-Strauss Syndrome", "strauss churg syndrome", "churg strauss syndrome", "churg-strauss syndrome", "Allergic granulomatosis", "allergic granulomatoses", "allergic granulomatosis", "Allergic Granulomatosis", "Allergic Granulomatoses", "Syndrome, Churg-Strauss", "syndrome, Churg-Strauss", "granulomatoses, allergic", "churg strauss vasculitis", "churg-strauss vasculitis", "Churg-Strauss vasculitis", "Granulomatoses, Allergic", "Churg-Strauss Vasculitis", "Granulomatosis, Allergic", "granulomatosis, allergic", "vasculitis, Churg-Strauss", "Vasculitis, Churg Strauss", "Vasculitis, Churg-Strauss", "vasculitis, Churg Strauss", "CSS - Churg-Strauss syndrome", "Granulomatous Allergic Angiitis", "Allergic Granulomatous Angiitis", "Allergic granulomatous angiitis", "allergic granulomatous angiitis", "granulomatous allergic angiitis", "Granulomatous allergic angiitis", "Angiitis, Granulomatous Allergic", "allergic; granulomatous angiitis", "angiitis, granulomatous allergic", "allergic granulomatosis angiitis", "granulomatous angiitis, allergic", "Allergic Angiitis, Granulomatous", "Allergic granulomatosis angiitis", "Granulomatous Angiitis, Allergic", "angiitis, allergic granulomatous", "allergic angiitis, granulomatous", "angiitis; allergic granulomatous", "Angiitis, Allergic Granulomatous", "ANGIITIS, ALLERGIC GRANULOMATOUS", "allergic granulomatous Angiitides", "granulomatous allergic Angiitides", "Allergic Granulomatous Angiitides", "Granulomatous Allergic Angiitides", "allergic; angiitis, granulomatous", "Angiitides, Granulomatous Allergic", "Granulomatous Angiitides, Allergic", "angiitides, granulomatous allergic", "granulomatous angiitides, allergic", "Angiitides, Allergic Granulomatous", "angiitides, allergic granulomatous", "allergic angiitides, granulomatous", "Allergic Angiitides, Granulomatous", "Allergic Granulomatous and Angiitis", "allergic granulomatous and angiitis", "Allergic Angiitis and Granulomatosis", "allergic angiitis and granulomatosis", "eosinophilic granulomatous vasculitis", "Eosinophilic Granulomatous Vasculitis", "Eosinophilic granulomatous vasculitis", "Granulomatous Vasculitis, Eosinophilic", "vasculitis, eosinophilic granulomatous", "Vasculitis, Eosinophilic Granulomatous", "granulomatous vasculitis, eosinophilic", "Eosinophilic Granulomatous Vasculitides", "eosinophilic granulomatous Vasculitides", "Granulomatous Vasculitides, Eosinophilic", "vasculitides, eosinophilic granulomatous", "ALLERGIC GRANULOMATOSIS OF CHURG-STRAUSS", "granulomatous vasculitides, eosinophilic", "Vasculitides, Eosinophilic Granulomatous", "Allergic granulomatosis angiitis (disorder)", "allergic granulomatous angiitis (diagnosis)", "Eosinophilic Granulomatosis with Polyangiitis", "eosinophilic granulomatosis with polyangiitis", "Eosinophilic granulomatosis with polyangiitis", "allergic granulomatous angiitis (Churg-Strauss)", "Polyarteritis with lung involvement [Churg-Strauss]", "EGPA - eosinophilic granulomatosis with polyangiitis", "Eosinophilic granulomatosis with polyangiitis [EGPA]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eosinophilic granulomatosis with polyangiitis", "shortest_name_length": 3}
{"curie": "MONDO:0008417", "names": ["SCLEROCORNEA, AUTOSOMAL DOMINANT", "Sclerocornea, Autosomal Dominant", "sclerocornea, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sclerocornea, autosomal dominant", "shortest_name_length": 32}
{"curie": "MONDO:0014896", "names": ["MDCDC", "Congenital muscular dystrophy Davignon Chauveau type", "Congenital muscular dystrophy, Davignon-Chauveau type", "congenital muscular dystrophy, Davignon-Chauveau type", "muscular dystrophy, congenital, Davignon-Chauveau type", "MUSCULAR DYSTROPHY, CONGENITAL, DAVIGNON-CHAUVEAU TYPE", "congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome", "Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome", "Congenital muscular dystrophy, respiratory failure, skin abnormalities, joint hyperlaxity syndrome", "Congenital muscular dystrophy, respiratory failure, skin abnormalities, joint hyperlaxity syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C1336075", "names": ["Splenic Small Lymphocytic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Splenic Small Lymphocytic Lymphoma", "shortest_name_length": 34}
{"curie": "MONDO:0010309", "names": ["MRX42", "XLID42", "X-linked mental retardation 42", "Mental Retardation, X-Linked 42", "MENTAL RETARDATION, X-LINKED 4S", "mental retardation, X-linked 42", "intellectual disability, X-linked 42", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 42", "non-syndromic X-linked intellectual disability 42"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 42", "shortest_name_length": 5}
{"curie": "UMLS:C5418965", "names": ["Ovarian Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Neuroendocrine Carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0006186", "names": ["Duodenal cancer", "Duodenal Cancer", "DUODENAL CANCER", "Duodenum Cancer", "Duodenum--Cancer", "Cancer, Duodenal", "Cancer of Duodenum", "duodenum carcinoma", "duodenal carcinoma", "CARCINOMA DUODENUM", "Duodenal Carcinoma", "Duodenal carcinoma", "Carcinoma duodenum", "DUODENAL CARCINOMA", "Duodenal cancer NOS", "Carcinoma of duodenum", "carcinoma of duodenum", "Carcinoma of Duodenum", "Duodenal carcinoma NOS", "Cancer of the Duodenum", "Duodenal Adenocarcinoma", "Duodenal adenocarcinoma", "duodenal adenocarcinoma", "adenocarcinoma duodenum", "duodenum adenocarcinoma", "Carcinoma of the Duodenum", "adenocarcinoma of duodenum", "Adenocarcinoma of Duodenum", "Adenocarcinoma of duodenum", "Adenocarcinoma of the Duodenum", "adenocarcinoma of the duodenum", "Carcinoma of duodenum (disorder)", "Carcinoma of duodenum (diagnosis)", "Adenocarcinoma of duodenum (disorder)", "Adenocarcinoma of duodenum (diagnosis)", "small intestine neoplasm malignant duodenum carcinoma", "small intestine neoplasm malignant adenocarcinoma of duodenum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "duodenal adenocarcinoma", "shortest_name_length": 15}
{"curie": "MONDO:0002095", "names": ["vascular tumors", "vascular cancer", "blood vessel tumor", "Blood vessel tumor", "Great Vessel Tumor", "vasculature cancer", "blood vessel tumors", "Blood vessel tumors", "Tumor of Great Vessel", "Great Vessel Neoplasm", "cancer of vasculature", "blood vessel neoplasm", "Haemangiomatous tumour", "pulmonary artery cancer", "malignant vascular tumor", "Malignant Vascular Tumor", "Neoplasm of Great Vessel", "neoplasm of great vessel", "vascular tissue neoplasm", "Neoplasm of great vessels", "Renal Vein Leiomyosarcoma", "renal vein leiomyosarcoma", "Neoplasms, Vascular Tissue", "malignant vascular neoplasm", "Malignant Vascular Neoplasm", "Leiomyosarcoma of Renal Vein", "malignant blood vessel tumor", "malignant great vessel tumor", "blood vessel tumour disorder", "Blood vessel tumour disorder", "Malignant Blood Vessel Tumor", "Vascular Neoplasms, Malignant", "vascular neoplasms, malignant", "malignant vasculature neoplasm", "Malignant Vascular Tissue Tumor", "cancerous tumor of blood vessel", "malignant tumor of blood vessel", "malignant blood vessel neoplasm", "malignant vascular tissue tumor", "Malignant Blood Vessel Neoplasm", "Cancerous Tumor of Blood Vessel", "Malignant blood vessel neoplasm", "Malignant Tumor of Blood Vessel", "Leiomyosarcoma of the Renal Vein", "leiomyosarcoma of the renal vein", "leiomyosarcoma of the renal Vein", "Malignant Pulmonary Vein Neoplasm", "malignant tumor of pulmonary vein", "Malignant Tumor of Pulmonary Vein", "malignant neoplasm of vasculature", "malignant tumor of pulmonary Vein", "pulmonary vein malignant neoplasm", "adult malignant vascular neoplasm", "malignant neoplasm of blood vessel", "Malignant neoplasm of blood vessel", "malignant vascular tissue neoplasm", "Malignant Vascular Tissue Neoplasm", "Malignant Tumor of Pulmonary Artery", "Malignant Pulmonary Artery Neoplasm", "malignant tumor of pulmonary artery", "pulmonary artery malignant neoplasm", "Malignant Neoplasm of Pulmonary Vein", "Neoplasm of great vessels (disorder)", "Malignant Tumor of the Pulmonary Vein", "Neoplasm of great vessels (diagnosis)", "Malignant Neoplasm of Pulmonary Artery", "Malignant neoplasm of blood vessel, NOS", "Malignant Tumor of the Pulmonary Artery", "Malignant Neoplasm of the Pulmonary Vein", "Malignant Neoplasm of the Pulmonary Artery", "neoplasm - soft tissue blood vessels great", "Primary malignant neoplasm of great vessels", "blood vessel tumor (morphologic abnormality)", "Malignant neoplasm of blood vessel (disorder)", "blood vessel tumors (morphologic abnormality)", "malignant neoplasm of blood vessel (diagnosis)", "neoplasm - soft tissue types blood vessel malignant", "Primary malignant neoplasm of great vessels (disorder)", "Primary malignant neoplasm of great vessels (diagnosis)", "Malignant blood vessel neoplasm (morphologic abnormality)", "neoplasm - soft tissue types great vessels malignant primary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vascular cancer", "shortest_name_length": 15}
{"curie": "MONDO:0019535", "names": ["drug-induced AIHA", "Drug-induced AIHA", "anemia hemolytic drug-induced autoimmune", "Drug induced autoimmune hemolytic anemia", "drug-induced autoimmune hemolytic anemia", "Drug-induced autoimmune hemolytic anemia", "Autoimmune hemolytic anemia, drug-induced", "anemia; hemolytic drug-induced, autoimmune", "Drug induced autoimmune haemolytic anaemia", "Drug-induced autoimmune haemolytic anaemia", "Drug-induced autoimmune hemolytic anemia (disorder)", "drug-induced autoimmune hemolytic anemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "drug-induced autoimmune hemolytic anemia", "shortest_name_length": 17}
{"curie": "MONDO:0001213", "names": ["serous glue ear", "Glue ear - serous", "OTITIS MEDIA SEROUS CHRONIC", "Chronic serous otitis media", "chronic serous otitis media", "Otitis media serous chronic", "serous otitis media, chronic", "otitis; media, serous, chronic", "otitis; media, chronic, serous", "Otitis media serous chronic NOS", "catarrhal; otitis media, chronic", "Chronic serous otitis media, NOS", "otitis; media, chronic, catarrhal", "media; otitis, chronic, catarrhal", "otitis; media, catarrhal, chronic", "Simple chronic serous otitis media", "Otitis media with effusion - serous", "chronic secretory otitis media, serous", "Chronic secretory otitis media, serous", "Chronic serous otitis media (disorder)", "Simple chronic serous otitis media, NOS", "chronic serous otitis media (diagnosis)", "Chronic serous otitis media, unspecified ear", "Chronic non-suppurative otitis media with effusion - serous"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "serous glue ear", "shortest_name_length": 15}
{"curie": "MONDO:0013903", "names": ["NYS7", "congenital nystagmus 7", "autosomal dominant congenital nystagmus 7", "nystagmus 7, congenital, autosomal dominant", "NYSTAGMUS 7, CONGENITAL, AUTOSOMAL DOMINANT", "NYSTAGMUS 7, congenital, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nystagmus 7, congenital, autosomal dominant", "shortest_name_length": 4}
{"curie": "MONDO:0014489", "names": ["MDDGC12", "LGMD due to POMK deficiency", "muscular dystrophy-dystroglycanopathy type C12", "Limb girdle muscular dystrophy due to POMK deficiency", "limb-girdle muscular dystrophy due to POMK deficiency", "Limb-girdle muscular dystrophy due to POMK deficiency", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 12", "muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 12", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, POMK-RELATED", "muscular dystrophy-dystroglycanopathy, limb-girdle, POMK-related", "Limb girdle muscular dystrophy due to protein O-mannose kinase deficiency", "Limb girdle muscular dystrophy due to protein O-mannose kinase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "limb-girdle muscular dystrophy due to POMK deficiency", "shortest_name_length": 7}
{"curie": "MONDO:0100430", "names": ["fibrotic liver disease", "liver fibrosis (disease)", "hepatic fibrosis (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibrotic liver disease", "shortest_name_length": 22}
{"curie": "UMLS:C0796624", "names": ["stage IV soft tissue sarcoma", "Stage IV Soft Tissue Sarcoma", "Stage IV Sarcoma of Soft Tissue", "Stage IV Sarcoma of the Soft Tissue", "Stage IV Soft Tissue Sarcoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Soft Tissue Sarcoma AJCC v7", "shortest_name_length": 28}
{"curie": "UMLS:C5446571", "names": ["Conjunctival Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conjunctival Stromal Tumor", "shortest_name_length": 26}
{"curie": "MONDO:0022768", "names": ["chronic polyradiculoneuritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic polyradiculoneuritis", "shortest_name_length": 28}
{"curie": "MONDO:0003330", "names": ["obstruction urinary", "Urinary obstruction", "urinary obstruction", "URINARY OBSTRUCTION", "obstruction; urinary", "Uropathy obstructive", "obstructive uropathy", "urinary; obstruction", "UROPATHY OBSTRUCTIVE", "Obstructive Uropathy", "Obstructive uropathy", "OBSTRUCTIVE UROPATHY", "obstructive; uropathy", "uropathy; obstructive", "obstructive uropathies", "Obstructive uropathy NOS", "obstruction tract urinary", "OBSTRUCTIVE UROPATHY, NOS", "URINARY TRACT OBSTRUCTION", "Urinary tract obstruction", "obstruction urinary tract", "Urinary Tract Obstruction", "Obstructive uropathy, NOS", "urinary tract obstruction", "obstructions tract urinary", "Urinary tract obstruction NOS", "Urinary tract obstruction, NOS", "Urinary (tract) obstruction NOS", "urinary obstruction (diagnosis)", "Urinary obstruction unspecified", "obstructive uropathy (diagnosis)", "Urinary obstruction, unspecified", "Urinary tract obstruction (disorder)", "urinary tract obstruction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urinary tract obstruction", "shortest_name_length": 19}
{"curie": "MONDO:0003735", "names": ["immature teratoma", "CNS Immature Teratoma", "CNS immature teratoma", "Immature Teratoma of CNS", "immature teratoma of CNS", "Immature Teratoma of the CNS", "immature teratoma of the CNS", "Immature teratoma of the CNS", "Central Nervous System Immature Teratoma", "central nervous system immature teratoma", "Immature Teratoma of Central Nervous System", "immature teratoma of central nervous system", "immature teratoma of the central nervous system", "Immature Teratoma of the Central Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system immature teratoma", "shortest_name_length": 17}
{"curie": "MONDO:0002377", "names": ["Intracanalicular fibroadenoma", "Intracanalicular Fibroadenoma", "intracanalicular fibroadenoma", "Intracanalicular fibroadenoma, NOS", "Intracanalicular Breast Fibroadenoma", "intracanalicular breast fibroadenoma", "breast intracanalicular fibroadenoma", "Breast Intracanalicular Fibroadenoma", "BREAST, FIBROADENOMA, INTRACANALICULAR", "Intracanalicular Fibroadenoma of Breast", "intracanalicular fibroadenoma of breast", "intracanalicular fibroadenoma of the breast", "Intracanalicular Fibroadenoma of the Breast", "Intracanalicular fibroadenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast intracanalicular fibroadenoma", "shortest_name_length": 29}
{"curie": "MONDO:0022866", "names": ["corneal dystrophy pigmentary anomaly malabsorption"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal dystrophy pigmentary anomaly malabsorption", "shortest_name_length": 50}
{"curie": "UMLS:C0019208", "names": ["Novikoff Hepatoma", "Hepatoma, Novikoff"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatoma, Novikoff", "shortest_name_length": 17}
{"curie": "MONDO:0000328", "names": ["hyperphosphatemia", "HYPERPHOSPHATEMIA", "Hyperphosphatemia", "hyperphosphataemia", "Hyperphosphatemias", "HYPERPHOSPHATAEMIA", "Hyperphosphataemia", "SERUM PHOSPHATE ELEVATED", "Serum phosphate increased", "High blood phosphate levels", "hyperphosphatemia (disease)", "Hyperphosphatemia (disorder)", "hyperphosphatemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperphosphatemia", "shortest_name_length": 17}
{"curie": "MONDO:0032666", "names": ["EV4", "RhoH Deficiency", "epidermodysplasia verruciformis, susceptibility to, 4", "Epidermodysplasia Verruciformis, Susceptibility to, 4", "EPIDERMODYSPLASIA VERRUCIFORMIS, SUSCEPTIBILITY TO, 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermodysplasia verruciformis, susceptibility to, 4", "shortest_name_length": 3}
{"curie": "UMLS:C0521530", "names": ["Consolidation", "Consolidation;lung", "Lung consolidation", "lung consolidation", "consolidation lung", "consolidation lungs", "Lung consolidations", "Air-Space Shadowing", "Airspace Consolidation", "Airspace Opacification", "PULMONARY CONSOLIDATION", "Pulmonary consolidation", "Air Space Opacification", "Pulmonary Consolidation", "pulmonary consolidation", "Consolidation of lung, NOS", "Lung consolidation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung consolidation", "shortest_name_length": 13}
{"curie": "UMLS:C5204545", "names": ["Bladder Neuroendocrine Tumor", "Bladder Well Differentiated Neuroendocrine Tumor", "Bladder Well-Differentiated Neuroendocrine Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder Neuroendocrine Tumor", "shortest_name_length": 28}
{"curie": "UMLS:C1333270", "names": ["Deletion of Chromosome 3p Associated Meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Deletion of Chromosome 3p Associated Meningioma", "shortest_name_length": 47}
{"curie": "MONDO:0020855", "names": ["SPGF32", "SPERMATOGENIC FAILURE 32", "spermatogenic failure 32"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 32", "shortest_name_length": 6}
{"curie": "UMLS:C1332146", "names": ["Acute Adult T-Cell Leukemia/Lymphoma", "Acute Adult T-Cell Lymphoma/Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Adult T-Cell Leukemia/Lymphoma", "shortest_name_length": 36}
{"curie": "UMLS:C0043252", "names": ["gunshot", "GUNSHOT WOUND", "gunshot wound", "Gunshot Wound", "Gunshot wound", "Gunshot Wounds", "gunshot wounds", "Wound, Gunshot", "Wound, gunshot", "Gunshot wounds", "GUNSHOT WOUNDS", "gunshot injury", "Gun shot wound", "Wound, shotgun", "GUNSHOT INJURY", "Wounds, Gunshot", "gunshot injuries", "Gunshot wound NOS", "Gunshot wound, NOS", "GSW - Gun shot wound", "Gunshot wound (disorder)", "gunshot wound (diagnosis)", "Gunshot wound (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gunshot wound", "shortest_name_length": 7}
{"curie": "UMLS:C0472713", "names": ["Nephrogenic anemia", "Nephrogenic anaemia", "anemia renal disease", "anemia disease renal", "anemia of renal disease", "Anemia of renal disease", "Anaemia of renal disease", "Anemia of renal disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anemia of renal disease", "shortest_name_length": 18}
{"curie": "MONDO:0009109", "names": ["LPI", "Congenital lysinuria", "dibasic aminoaciduria 2", "dibasic amino aciduria 2", "Dibasicamino aciduria II", "Dibasic Amino Aciduria II", "DIBASIC AMINO ACIDURIA II", "dibasic amino aciduria II", "Hyperdibasic Aminoaciduria", "Hyperdibasic aminoaciduria", "hyperdibasic aminoaciduria", "Lysinuric Protein Intolerance", "lysinuric PROTEIN intolerance", "lysinuric protein intolerance", "LYSINURIC PROTEIN INTOLERANCE", "Lysinuric protein intolerance", "Hyperdibasic aminoaciduria, NOS", "hyperdibasic aminoaciduria type 2", "Lysinuric protein intolerance, NOS", "LPI - Lysinuric Protein Intolerance", "LPI - Lysinuric protein intolerance", "Lysinuric protein intolerance (disorder)", "lysinuric protein intolerance (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lysinuric protein intolerance", "shortest_name_length": 3}
{"curie": "UMLS:C1956260", "names": ["Cavernous Angioma, Central Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cavernous Angioma, Central Nervous System", "shortest_name_length": 41}
{"curie": "UMLS:C0853330", "names": ["Peripheral neuropathy aggravated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peripheral neuropathy aggravated", "shortest_name_length": 32}
{"curie": "MONDO:0016785", "names": ["CHM", "Complete Mole", "complete Mole", "Vesicular mole", "vesicular mole", "MOLE, VESICULAR", "Vesicular mole NOS", "Complete Hydatid Mole", "complete hydatid Mole", "Complete Molar Pregnancy", "Complete molar pregnancy", "complete molar pregnancy", "Complete hydatidiform mole", "complete hydatidiform mole", "Complete Hydatidiform Mole", "complete; hydatidiform mole", "HYDATIDIFORM MOLE, COMPLETE", "Mole, Complete Hydatidiform", "Classical Hydatidiform Mole", "Hydatidiform Mole, Complete", "hydatidiform mole; complete", "Complete Hydatidiform Moles", "classical hydatidiform Mole", "Moles, Complete Hydatidiform", "Hydatidiform Moles, Complete", "mole; hydatidiform, complete", "CHM - Complete hydatidiform mole", "Complete hydatidiform mole (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complete hydatidiform mole", "shortest_name_length": 3}
{"curie": "MONDO:0015086", "names": ["Benallegue-Lacete syndrome", "Benallegue Lacete syndrome", "cloverleaf skull and asphyxiating thoracic dysplasia", "cloverleaf skull-asphyxiating thoracic dysplasia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cloverleaf skull-asphyxiating thoracic dysplasia syndrome", "shortest_name_length": 26}
{"curie": "UMLS:C5420024", "names": ["Sinonasal Spindle Cell Squamous Cell Carcinoma", "Sinonasal Spindle Cell (Sarcomatoid) Squamous Cell Carcinoma", "Nasal Cavity and Paranasal Sinus Spindle Cell Squamous Cell Carcinoma", "Nasal Cavity and Paranasal Sinus Spindle Cell (Sarcomatoid) Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Spindle Cell Squamous Cell Carcinoma", "shortest_name_length": 46}
{"curie": "MONDO:0013440", "names": ["LGMD2P", "MDDGC9", "LGMDR16", "LGMD type 2P", "Alpha-dystroglycan-related LGMD R16", "Limb-girdle muscular dystrophy type 2P", "limb-girdle muscular dystrophy type 2P", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2P", "muscular dystrophy, limb-girdle, type 2P", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 16", "DAG1 autosomal recessive limb-girdle muscular dystrophy", "Autosomal recessive limb-girdle muscular dystrophy type 2P", "Autosomal recessive limb girdle muscular dystrophy type 2P", "autosomal recessive limb-girdle muscular dystrophy type 2P", "muscular dystrophy-dystroglycanopathy (limb-girdle) type C9", "Alpha-dystroglycan-related limb-girdle muscular dystrophy R16", "muscular dystrophy-dystroglycanopathy limb-girdle DAG1-related", "muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 9", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 9", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, DAG1-RELATED", "muscular dystrophy-dystroglycanopathy, limb-girdle, Dag1-related", "Autosomal recessive limb girdle muscular dystrophy type 2P (disorder)", "autosomal recessive limb-girdle muscular dystrophy caused by mutation in DAG1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive limb-girdle muscular dystrophy type 2P", "shortest_name_length": 6}
{"curie": "UMLS:C5556687", "names": ["Minor Salivary Gland IPMN", "Minor Salivary Gland Intraductal Papillary-Mucinous Neoplasm", "Minor Salivary Gland Intraductal Papillary Mucinous Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Minor Salivary Gland Intraductal Papillary-Mucinous Neoplasm", "shortest_name_length": 25}
{"curie": "UMLS:C5421216", "names": ["Visual Pathway Melanocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Visual Pathway Melanocytoma", "shortest_name_length": 27}
{"curie": "MONDO:0020112", "names": ["vitamin B12- and folate-independent constitutional megaloblastic anemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitamin B12- and folate-independent constitutional megaloblastic anemia", "shortest_name_length": 71}
{"curie": "UMLS:C1333842", "names": ["Grade 3 Cutaneous Follicular Lymphoma", "Large B Cell Follicular Lymphoma of Skin", "Cutaneous Large B Cell Follicular Lymphoma", "Large B Cell Follicular Lymphoma of the Skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade 3 Cutaneous Follicular Lymphoma", "shortest_name_length": 37}
{"curie": "MONDO:0012216", "names": ["FVH2", "FHONDA", "FHONDA syndrome", "foveal hypoplasia 2", "FOVEAL HYPOPLASIA 2", "foveal hypoplasia type 2", "Foveal Hypoplasia and Anterior Segment Dysgenesis", "foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome", "foveal hypoplasia 2 with or without optic nerve misrouting and/or anterior segment dysgenesis", "FOVEAL HYPOPLASIA 2 WITH OR WITHOUT OPTIC NERVE MISROUTING AND/OR ANTERIOR SEGMENT DYSGENESIS", "foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis", "FOVEAL HYPOPLASIA 2 WITH OPTIC NERVE DECUSSATION DEFECTS AND ANTERIOR SEGMENT DYSGENESIS WITHOUT ALBINISM", "foveal hypoplasia 2 with optic nerve decussation defects and anterior segment dysgenesis without albinism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0008608", "names": ["DCR", "Down", "DSCR", "47,XX,+21", "47,XY,+21", "Trisomy G", "G Trisomy", "G trisomy", "Mongolism", "MONGOLISM", "mongolism", "trisomy 21", "Trisomy 21", "21 trisomy", "TRISOMY 21", "trisomy; 21", "morbus Down", "morbus down", "21 trisomies", "mongoloidism", "Langdon Down", "MONGOLOIDISM", "DOWN SYNDROME", "Down Syndrome", "Down syndrome", "Syndrome, Down", "Downs syndrome", "Downs Syndrome", "Trisomy 21 NOS", "Down's syndrome", "Syndrome Down's", "DOWN'S SYNDROME", "Down's Syndrome", "down s syndrome", "SYNDROME DOWN'S", "T21 - Trisomy 21", "Syndrome, Down's", "downing syndrome", "Trisomy 21 syndrome", "TRISOMY 21 SYNDROME", "trisomy 21 syndrome", "Trisomy 21 Syndrome", "Chromosome 21 trisomy", "Langdon Down syndrome", "syndrome; trisomy, 21", "trisomy; syndrome, 21", "chromosome; 21, trisomy", "trisomy 21 Down syndrome", "Down syndrome, unspecified", "trisomy 21 (Down syndrome)", "Trisomy 21 (Down Syndrome)", "complete trisomy 21 syndrome", "Complete trisomy 21 syndrome", "Down's syndrome - trisomy 21", "Down's syndrome, unspecified", "Down syndrome critical region", "DOWN SYNDROME CRITICAL REGION", "Down Syndrome Critical Region", "Down syndrome, Isolated cases", "congenital acromicria syndrome", "chromosome 21 trisomy syndrome", "DOWN SYNDROME CHROMOSOME REGION", "Down syndrome chromosome region", "Trisomy 21 (morphologic abnormality)", "trisomy 21 Down syndrome (diagnosis)", "Complete trisomy 21 syndrome (disorder)", "leukemia, megakaryoblastic, of Down syndrome", "Leukemia, Megakaryoblastic, of Down Syndrome", "LEUKEMIA, MEGAKARYOBLASTIC, OF DOWN SYNDROME", "Chromosomal imbalance syndrome, pair 21, trisomy", "transient myeloproliferative disorder of Down syndrome", "TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDROME", "Transient Myeloproliferative Disorder of Down Syndrome", "leukemia, megakaryoblastic, with or without Down syndrome, somatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Down syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0016958", "names": ["7q trisomy", "Trisomy 7q", "trisomy 7q", "7q+ syndrome", "7q duplication", "Duplication 7q", "dup(7q) syndrome", "partial trisomy 7q", "7q partial trisomy", "chromosome 7q trisomy", "7q duplication syndrome", "duplication 7q syndrome", "Chromosome 7, trisomy 7q", "chromosome 7q duplication", "7q partial trisomy syndrome", "7q partial trisomy (disorder)", "partial trisomy of chromosome 7q", "chromosome 7q duplication syndrome", "partial duplication of chromosome 7q", "partial trisomy of the long arm of chromosome 7", "partial duplication of the long arm of chromosome 7", "partial duplication of the long arm of chromosome type 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of the long arm of chromosome 7", "shortest_name_length": 10}
{"curie": "MONDO:0016365", "names": ["familial primary hyperparathyroidism", "hereditary primary hyperparathyroidism (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial primary hyperparathyroidism", "shortest_name_length": 36}
{"curie": "UMLS:C2347314", "names": ["Myxoid leiomyoma", "Myxoid Leiomyoma", "Myxoid leiomyoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myxoid leiomyoma", "shortest_name_length": 16}
{"curie": "UMLS:C4330849", "names": ["Occipital Lobe, Parietal Lobe, and Ventricular Ependymal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Occipital Lobe, Parietal Lobe, and Ventricular Ependymal Tumor", "shortest_name_length": 62}
{"curie": "UMLS:C1332878", "names": ["CNS Dermoid Cyst", "Dermoid Cyst of CNS", "Dermoid Cyst of the CNS", "Central Nervous System Dermoid Cyst", "Dermoid Cyst of Central Nervous System", "Dermoid Cyst of the Central Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Dermoid Cyst", "shortest_name_length": 16}
{"curie": "UMLS:C2748249", "names": ["Infective exacerbation of bronchiectasis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infective exacerbation of bronchiectasis", "shortest_name_length": 40}
{"curie": "UMLS:C4288067", "names": ["Unresectable Solid Tumor", "Unresectable Solid Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Solid Neoplasm", "shortest_name_length": 24}
{"curie": "MONDO:0018019", "names": ["PLUMBISM", "plumbism", "Plumbism", "Saturnism", "SATURNISM", "saturnism", "lead poison", "Lead Poisoning", "lead poisoning", "Poisoning;lead", "LEAD POISONING", "Lead poisoning", "painter's colic", "Lead Poisonings", "Poisoning, Lead", "Poisonings, Lead", "Lead intoxication", "poisoning by lead", "Saturnine poisoning", "Lead - toxic effect", "Lead poisoning syndrome", "Saturnine poisoning syndrome", "poisoning by lead (diagnosis)", "Poisoning by compounds of lead", "Toxic effect of lead compound, NOS", "Lead and/or lead compound poisoning", "Toxic effect of lead and its compounds", "Toxic effects of lead and its compounds", "Toxic effect of unspecified lead compound", "Toxic effects of lead and its compounds NOS", "Lead and lead compounds causing toxic effect", "Lead and/or lead compound poisoning (disorder)", "Toxic effect of lead and its compounds, including fumes", "Toxic effect of lead and its compounds (including fumes)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lead poisoning", "shortest_name_length": 8}
{"curie": "MONDO:0004847", "names": ["Cataract;senile", "cataract senile", "CATARACT SENILE", "Senile Cataract", "senile cataract", "Senile cataract", "cataracts senile", "Senile cataract, NOS", "Age-related cataract", "age-related cataract", "age related cataracts", "Old-age related cataract", "Senile cataract (disorder)", "senile cataract (diagnosis)", "Senile cataract, unspecified", "Clouding of the lens of the eye with age"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "senile cataract", "shortest_name_length": 15}
{"curie": "MONDO:0030019", "names": ["ANXD3", "ANAUXETIC DYSPLASIA 3", "anauxetic dysplasia 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anauxetic dysplasia 3", "shortest_name_length": 5}
{"curie": "MONDO:0014719", "names": ["DEE35", "EIEE35", "Martsolf-like syndrome", "ITPA-related encephalopathy", "early infantile epileptic encephalopathy 35", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 35", "developmental and epileptic encephalopathy 35", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 35", "epileptic encephalopathy, early infantile, 35", "developmental and epileptic encephalopathy, 35", "epileptic encephalopathy, early infantile, type 35", "ITPA-related lethal infantile neurological disorder with cataract and cardiac involvement", "Inosine triphosphate pyrophosphohydrolase-related lethal infantile neurological disorder with cataract and cardiac involvement", "Inosine triphosphate pyrophosphohydrolase-related lethal infantile neurological disorder with cataract and cardiac involvement (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 35", "shortest_name_length": 5}
{"curie": "UMLS:C1335525", "names": ["CCCH", "Prostatic CCCH", "CCCH of the Prostate", "Cribriform Prostate Hyperplasia", "Prostatic Cribriform Hyperplasia", "Cribriform Hyperplasia of Prostate", "Cribriform Hyperplasia of the Prostate", "Prostatic Clear Cell Cribriform Hyperplasia", "Clear Cell Cribriform Hyperplasia of the Prostate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostatic Clear Cell Cribriform Hyperplasia", "shortest_name_length": 4}
{"curie": "MONDO:0045023", "names": ["acquired adrenogenital syndrome", "Acquired adrenogenital syndrome", "ADRENOGENITAL SYNDROME, ACQUIRED", "acquired; adrenogenital syndrome", "adrenogenital; syndrome, acquired", "Acquired adrenogenital syndrome (disorder)", "acquired adrenogenital syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired adrenogenital syndrome", "shortest_name_length": 31}
{"curie": "MONDO:0016210", "names": ["Crossed hemiplegia", "Hemiplegia crossed", "Crossed Hemiplegia", "Crossed Hemiplegias", "Hemiplegia, Crossed", "Hemiplegia, crossed", "Alternate hemiplegia", "Hemiplegias, Crossed", "Hemiplegia, alternate", "alternating hemiplegia", "Alternating hemiplegia", "Crossed hemiplegia (disorder)", "Alternating hemiplegia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alternating hemiplegia", "shortest_name_length": 18}
{"curie": "MONDO:0000901", "names": ["relapsed/refractory diffuse large B-cell lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "relapsed/refractory diffuse large B-cell lymphoma", "shortest_name_length": 49}
{"curie": "MONDO:0016644", "names": ["LPA", "Logopenic variant PPA", "Lepidic Adenocarcinoma", "Lepidic adenocarcinoma", "logopenic progressive aphasia", "Logopenic progressive aphasia", "Lepidic predominant adenocarcinoma", "Lepidic Predominant Adenocarcinoma", "Logopenic primary progressive aphasia", "Lepidic Predominant Lung Adenocarcinoma", "Logopenic progressive aphasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "logopenic progressive aphasia", "shortest_name_length": 3}
{"curie": "MONDO:0021907", "names": ["aplasia cutis autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aplasia cutis autosomal recessive", "shortest_name_length": 33}
{"curie": "MONDO:0008667", "names": ["VHL", "VHLS", "Hippel", "Von Hippel", "VHL Syndrome", "VHL syndrome", "VHL Syndromes", "Lindau disease", "lindau disease", "Lindau Disease", "Lindaus Disease", "Lindau' disease", "Lindau's Disease", "Lindau's disease", "lindau's disease", "Lindau's Diseases", "Angiomatosis Retinae", "Hippel-Lindau Disease", "Hippel Lindau Disease", "hippel lindau disease", "hippel-lindau disease", "hippel lindau syndrome", "Hippel Lindau syndrome", "disease hippel-lindau von", "von Hippel Lindau Disease", "Von Hippel-Lindau disease", "Von Hippel Lindau disease", "Von Hippel-Lindau Disease", "VON HIPPEL LINDAU DISEASE", "von hippel-lindau disease", "von-hippel lindau disease", "VON HIPPEL-LINDAU DISEASE", "von Hippel-Lindau disease", "lindau von hippel disease", "hippel lindau von disease", "von Hippel-Lindau Disease", "von hippel lindau disease", "von Hippel Lindau Syndrome", "VON HIPPEL-LINDAU SYNDROME", "Von Hippel-Lindau syndrome", "disease hippel lindaus von", "von hippel lindau syndrome", "hippel lindau syndrome von", "von Hippel-Lindau Syndrome", "von Hippel-Lindau syndrome", "von hippel-lindau syndrome", "Von Hippel Lindau syndrome", "Von Hippel Lindau Syndrome", "Von Hippel-Lindau Syndrome", "cerebroretinal angiomatosis", "Cerebroretinal angiomatosis", "hippel lindaus syndrome von", "Cerebroretinal Angiomatosis", "VHL - von Hippel-Lindau syndrome", "Von Hippel-Lindau Syndrome (VHL)", "Von Hippel-Lindau syndrome (VHL)", "VHL (Von Hippel-Lindau) syndrome", "Von Hippel-Lindau syndrome (disorder)", "familial cerebelloretinal angiomatosis", "Familial cerebelloretinal angiomatosis", "Familial Cerebelloretinal Angiomatosis", "von Hippel-Lindau syndrome (diagnosis)", "Familial Cerebelloretinal Angiomatoses", "ANGIOPHAKOMATOSIS RETINAE ET CEREBELLI", "Angiomatoses, Familial Cerebelloretinal", "Familial Cerebello Retinal Angiomatosis", "Familial Cerebello-Retinal Angiomatosis", "von Hippel-Lindau syndrome, modifier of", "Cerebelloretinal Angiomatosis, Familial", "Familial Cerebello-Retinal Angiomatoses", "HEMANGIOBLASTOMATOSIS, CEREBELLORETINAL", "Angiomatosis, Familial Cerebelloretinal", "Familial cerebello-retinal angiomatosis", "Cerebelloretinal Angiomatoses, Familial", "Von Hippel-Lindau syndrome, Modifiers of", "Angiomatosis, Familial Cerebello-Retinal", "Cerebello-Retinal Angiomatoses, Familial", "Cerebello-Retinal Angiomatosis, Familial", "VON HIPPEL-LINDAU SYNDROME, MODIFIERS OF", "Angiomatoses, Familial Cerebello-Retinal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "von Hippel-Lindau disease", "shortest_name_length": 3}
{"curie": "UMLS:C2987253", "names": ["Esophageal Basal Cell Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Basal Cell Hyperplasia", "shortest_name_length": 33}
{"curie": "UMLS:C2985357", "names": ["Central Nervous System Histiocytic and Dendritic Cell Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Histiocytic and Dendritic Cell Neoplasm", "shortest_name_length": 62}
{"curie": "MONDO:0030056", "names": ["FRTS5", "Fanconi renotubular syndrome 5", "FANCONI RENOTUBULAR SYNDROME 5", "Acadian-variant Fanconi syndrome", "FANCONI RENOTUBULAR SYNDROME, ACADIAN VARIANT", "Fanconi Renotubular Syndrome, Acadian Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fanconi renotubular syndrome 5", "shortest_name_length": 5}
{"curie": "UMLS:C1333427", "names": ["EBV-Related Burkitt Lymphoma", "EBV Related Burkitt's Lymphoma", "EBV-Related Burkitt's Lymphoma", "Epstein-Barr Virus-Related Burkitt Lymphoma", "Epstein-Barr Virus-Related Burkitt's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "EBV-Related Burkitt Lymphoma", "shortest_name_length": 28}
{"curie": "MONDO:0001304", "names": ["benign hypertensive renal disease", "Benign hypertensive renal disease", "hypertensive renal disease, benign", "Hypertensive renal disease, benign", "Benign hypertensive renal disease (disorder)", "Hypertensive renal disease, benign, without mention of renal failure", "hypertensive renal disease, benign, without mention of renal failure", "Hypertensive chronic kidney disease, benign, with chronic kidney disease stage I through stage IV, or unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign hypertensive renal disease", "shortest_name_length": 33}
{"curie": "MONDO:0013251", "names": ["BIRBECK GRANULE DEFICIENCY", "Birbeck granule deficiency", "Birbeck granules, absence of", "BIRBECK GRANULES, ABSENCE OF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Birbeck granule deficiency", "shortest_name_length": 26}
{"curie": "UMLS:C0751113", "names": ["UNCINATE SEIZURE", "Uncinate Seizure", "seizure; uncinate", "Uncinate Seizures", "Seizure, Uncinate", "uncinate seizures", "Seizures, Uncinate", "uncinate; seizures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uncinate Seizures", "shortest_name_length": 16}
{"curie": "UMLS:C4525131", "names": ["Stage IVC Colon Cancer", "stage IVC colon cancer", "stage IVC colon cancer AJCC v8", "Stage IVC Colon Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Colon Cancer AJCC v8", "shortest_name_length": 22}
{"curie": "MONDO:0003093", "names": ["Esophageal Mucoepidermoid Cancer", "Mucoepidermoid Esophagus Carcinoma", "esophagus mucoepidermoid carcinoma", "mucoepidermoid esophageal carcinoma", "Mucoepidermoid Esophageal Carcinoma", "Esophageal Mucoepidermoid Carcinoma", "Mucoepidermoid Carcinoma of Esophagus", "mucoepidermoid carcinoma of esophagus", "Mucoepidermoid Carcinoma of the Esophagus", "Mucoepidermoid carcinoma of the esophagus", "mucoepidermoid carcinoma of the esophagus", "mucoepidermoid carcinoma of esophagus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucoepidermoid esophageal carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0016106", "names": ["progressive muscular dystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive muscular dystrophy", "shortest_name_length": 30}
{"curie": "MONDO:0007777", "names": ["HTRDC", "Hypertaurinuric Cardiomyopathy", "HYPOTAURINEMIC RETINAL DEGENERATION AND CARDIOMYOPATHY", "hypotaurinemic retinal degeneration and cardiomyopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotaurinemic retinal degeneration and cardiomyopathy", "shortest_name_length": 5}
{"curie": "MONDO:0021456", "names": ["Benign Sternal Tumor", "benign sternal tumor", "sternum benign neoplasm", "Benign Tumor of Sternum", "benign sternal neoplasm", "benign tumor of sternum", "Benign Sternal Neoplasm", "benign neoplasm of sternum", "Benign Neoplasm of Sternum", "Benign neoplasm of sternum", "Benign Tumor of the Sternum", "benign tumor of the sternum", "benign neoplasm of the sternum", "Benign Neoplasm of the Sternum", "Benign neoplasm of sternum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of sternum", "shortest_name_length": 20}
{"curie": "MONDO:0015611", "names": ["Chanarin-Dorfman syndrome", "neutral lipid storage disease", "lipidosis with triglycerid storage disease", "lipidosis with triglyceride storage disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neutral lipid storage disease", "shortest_name_length": 25}
{"curie": "UMLS:C4683579", "names": ["Lugano Classification Stage IIE Adult Non-Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage IIE Adult Non-Hodgkin Lymphoma AJCC v8", "shortest_name_length": 66}
{"curie": "MONDO:0006771", "names": ["glossitis", "GLOSSITIS", "Glossitis", "Glossitides", "Glossitis, NOS", "Tongue inflamed", "Inflammation tongue", "INFLAMMATION TONGUE", "Tongue inflammation", "tongue inflammation", "inflammation tongue", "TONGUE INFLAMMATION", "Lingual inflammation", "tongue; inflammation", "inflammation; tongue", "Glossitis (disorder)", "glossitis (diagnosis)", "Smooth swollen tongue", "inflammation of tongue", "Inflammation of tongue", "Inflammation of the tongue", "inflammation of tongue (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glossitis", "shortest_name_length": 9}
{"curie": "MONDO:0007574", "names": ["SCA34", "Giroux Barbeau Syndrome", "Giroux Barbeau syndrome", "SPINOCEREBELLAR ATAXIA 34", "spinocerebellar ataxia 34", "Erythrokeratodermia ataxia", "erythrokeratodermia - ataxia", "spinocerebellar ataxia type 34", "Spinocerebellar ataxia type 34", "erythrokeratodermia with ataxia", "Erythrokeratodermia with ataxia", "ERYTHROKERATODERMIA WITH ATAXIA", "Spinocerebellar ataxia type 34 (disorder)", "spinocerebellar ataxia and erythrokeratodermia", "Spinocerebellar ataxia and erythrokeratodermia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia type 34", "shortest_name_length": 5}
{"curie": "UMLS:C0280962", "names": ["Myelosuppression", "Bone Marrow Depression", "Bone Marrow Suppression", "Bone marrow suppression", "bone marrow suppression", "BONE MARROW SUPPRESSION", "suppression, bone marrow"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone Marrow Suppression", "shortest_name_length": 16}
{"curie": "MONDO:0005116", "names": ["whipple disease", "Whipple disease", "disease whipple", "Whipple Disease", "Disease, Whipple", "Whipples Disease", "whipples disease", "WHIPPLES DISEASE", "Whipples disease", "whipple's disease", "disease whipple's", "Whipple's disease", "Whipple's Disease", "Disease, Whipple's", "WD - Whipple's disease", "Intestinal Lipodystrophy", "intestinal lipodystrophy", "INTESTINAL LIPODYSTROPHY", "Intestinal lipodystrophy", "lipodystrophy; intestinal", "Lipodystrophy, Intestinal", "LIPODYSTROPHY, INTESTINAL", "intestinal; lipodystrophy", "Secondary Non-tropical Sprue", "Whipple's disease (disorder)", "Intestinal Whipple's disease", "secondary non-tropical sprue", "Whipple's disease (diagnosis)", "SPRUE, NONTROPICAL, SECONDARY", "Tropheryma whippelii infection", "intestinal lipophagic granulomatosis", "Intestinal lipophagic granulomatosis", "GRANULOMATOSIS, LIPOPHAGIC, INTESTINAL", "Tropheryma whipplei infectious disease", "Tropheryma whipplei disease or disorder", "Tropheryma whipplei caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Whipple disease", "shortest_name_length": 15}
{"curie": "UMLS:C1142158", "names": ["Hepatic vein occlusion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatic vein occlusion", "shortest_name_length": 22}
{"curie": "MONDO:0002353", "names": ["Glottis Tumor", "glottis tumor", "Tumor of Glottis", "tumor of glottis", "glottis neoplasm", "Tumor of glottis", "Glottis Neoplasm", "Tumour of glottis", "Neoplasm of glottis", "Neoplasm of Glottis", "neoplasm of glottis", "tumor of the Glottis", "Tumor of the Glottis", "tumor of the glottis", "neoplasm of the glottis", "Neoplasm of the Glottis", "glottis neoplasm (disease)", "Neoplasm of glottis (disorder)", "neoplasm of glottis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glottis neoplasm", "shortest_name_length": 13}
{"curie": "MONDO:0032789", "names": ["MRT71", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 71", "Mental Retardation, Autosomal Recessive 71", "autosomal recessive intellectual developmental disorder 71", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 71", "intellectual developmental disorder, autosomal recessive 71"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder, autosomal recessive 71", "shortest_name_length": 5}
{"curie": "UMLS:C1335389", "names": ["Neural Fibrolipoma", "Lipomatosis of Nerve", "Peripheral Nerve Fibrolipomatous Hamartoma", "Fibrolipomatous Hamartoma of Peripheral Nerve"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lipomatosis of Nerve", "shortest_name_length": 18}
{"curie": "MONDO:0006777", "names": ["TONGUE HAIRY", "hairy tongue", "Hairy tongue", "tongue hairy", "Hairy Tongue", "Tongue black", "Black tongue", "Tongue hairy", "Black;tongue", "tongue black", "Lingua Nigra", "TONGUE BLACK", "black tongue", "hairy Tongues", "nigra; lingua", "Tongue, Hairy", "Hairy Tongues", "Trichoglossia", "Melanoglossia", "hairy tongues", "black tongues", "lingua; nigra", "melanoglossia", "Tongues, Hairy", "Tongues, hairy", "blacking tongue", "Tongue black hairy", "Tongue black furry", "hairy black tongue", "tongue hairy black", "black furry tongue", "black hairy tongue", "Black hairy tongue", "TONGUE BLACK FURRY", "hairy tongue; black", "black; hairy tongue", "Lingua Villosa Nigra", "Lingua villosa nigra", "Black hairy tongue (disorder)", "black hairy tongue (diagnosis)", "Overgrowth of filiform papillae", "hairy tongue (physical finding)", "overgrowth of filiform papillae", "Hypertrophy of filiform papillae", "Overgrowth of filiform papillae (disorder)", "tongue papillae hypertrophy black hairy tongue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hairy tongue", "shortest_name_length": 12}
{"curie": "UMLS:C4683693", "names": ["Nasal Type NK/T-Cell Lymphoma by Ann Arbor Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasal Type NK/T-Cell Lymphoma by Ann Arbor Stage", "shortest_name_length": 48}
{"curie": "MONDO:0014435", "names": ["BBS7", "BARDET-BIEDL SYNDROME 7", "Bardet-Biedl syndrome 7", "Bardet-Biedl Syndrome 7", "BBS7 Bardet-Biedl syndrome", "Bardet-Biedl syndrome type 7", "Bardet-Biedl syndrome caused by mutation in BBS7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bardet-Biedl syndrome 7", "shortest_name_length": 4}
{"curie": "UMLS:C5419433", "names": ["Unspecified Eye/Vision Problem", "Unspecified Eye / Vision Problem"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unspecified Eye/Vision Problem", "shortest_name_length": 30}
{"curie": "MONDO:0012101", "names": ["JOAG2", "GLC1J", "JOAG1J", "Glaucoma 1, Open Angle, J", "glaucoma 1, open angle, J", "GLAUCOMA 1, OPEN ANGLE, J", "glaucoma, primary open angle, juvenile-onset, 2", "GLAUCOMA, PRIMARY OPEN ANGLE, JUVENILE-ONSET, 2", "Glaucoma, Primary Open Angle, Juvenile-Onset, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glaucoma 1, open angle, J", "shortest_name_length": 5}
{"curie": "UMLS:C3273030", "names": ["Liver Neuroendocrine Neoplasm", "Hepatic Neuroendocrine Neoplasm", "Primary Liver Neuroendocrine Neoplasm", "Primary Hepatic Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liver Neuroendocrine Neoplasm", "shortest_name_length": 29}
{"curie": "MONDO:0035650", "names": ["Late-onset Steinert disease", "Late-onset myotonic dystrophy type 1", "late-onset Steinert myotonic dystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "late-onset Steinert myotonic dystrophy", "shortest_name_length": 27}
{"curie": "UMLS:C1735373", "names": ["Acute uveitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute uveitis", "shortest_name_length": 13}
{"curie": "MONDO:0010590", "names": ["OKS", "FGS", "FGS1", "FG syndrome", "fg syndrome", "FG SYNDROME", "fgs syndrome", "FG SYNDROME 1", "FG syndrome 1", "KELLER SYNDROME", "Keller syndrome", "MED12 FG syndrome", "FG Syndrome Type 1", "FG syndrome type 1", "FG syndrome (disorder)", "opitz-kaveggia syndrome", "Opitz-Kaveggia syndrome", "Opitz-Kaveggia Syndrome", "Opitz Kaveggia syndrome", "OPITZ-KAVEGGIA SYNDROME", "FG syndrome type 1 (disorder)", "FG syndrome caused by mutation in MED12", "Opitz-Kaveggia syndrome, X-linked recessive", "mental retardation, large head, imperforate anus, congenital hypotonia, and partial agenesis of corpus callosum", "MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA, AND PARTIAL AGENESIS OF CORPUS CALLOSUM", "Mental Retardation, Large Head, Imperforate Anus, Congenital Hypotonia, and Partial Agenesis of the Corpus Callosum", "intellectual disability, large head, imperforate anus, congenital hypotonia, and partial agenesis of corpus callosum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FG syndrome 1", "shortest_name_length": 3}
{"curie": "MONDO:0003306", "names": ["Ancient Neurofibroma", "atypical neurofibroma", "Atypical neurofibroma", "Neurofibroma with Atypia", "Atypical neurofibroma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical neurofibroma", "shortest_name_length": 20}
{"curie": "MONDO:0025376", "names": ["equine plague", "Equine Plague", "Equine Plagues", "plague, equine", "equine Plagues", "Plague, Equine", "Plagues, equine", "Plagues, Equine", "African Horsesickness", "African horse sickness", "African Horse Sickness", "Horsesickness, African", "sickness, African horse", "horse sickness, African", "African Horsesicknesses", "Horse Sickness, African", "Sickness, African Horse", "African horse Sicknesses", "Horsesicknesses, African", "African Horse Sicknesses", "Sicknesses, African Horse", "Horse Sicknesses, African", "Sicknesses, African horse", "horse Sicknesses, African", "African horse sickness (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "African horse sickness", "shortest_name_length": 13}
{"curie": "MONDO:0014925", "names": ["FFEVF3", "epilepsy, familial focal, with variable foci 3", "EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 3", "NPRL3 epilepsy, familial focal, with variable foci", "epilepsy, familial focal, with variable foci type 3", "epilepsy, familial focal, with variable foci 3; FFEVF3", "epilepsy, familial focal, with variable foci caused by mutation in NPRL3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, familial focal, with variable foci 3", "shortest_name_length": 6}
{"curie": "MONDO:0013595", "names": ["HBLVD", "green jaundice", "GREEN JAUNDICE", "Green jaundice", "hyperbiliverdinemia", "Hyperbiliverdinemia", "HYPERBILIVERDINEMIA", "Hyperbiliverdinaemia", "Hyperbiliverdinemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperbiliverdinemia", "shortest_name_length": 5}
{"curie": "UMLS:C1335045", "names": ["Non-Neoplastic Thoracic Disease", "Non-Neoplastic Thoracic Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Thoracic Disorder", "shortest_name_length": 31}
{"curie": "UMLS:C5555759", "names": ["Broad Ligament Wolffian Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Broad Ligament Wolffian Tumor", "shortest_name_length": 29}
{"curie": "UMLS:C1304306", "names": ["Metastatic Basal Cell Carcinoma", "Basal cell carcinoma metastatic", "Metastatic basal cell carcinoma", "Metastatic basal cell carcinoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic basal cell carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0011670", "names": ["clEDS", "EDSCLL", "clEDS type 1", "TNX DEFICIENCY", "TNX deficiency", "Tnx deficiency", "classical-like EDS", "EDS, classic-like type", "EDS due to TNX deficiency", "EDS DUE TO TNX DEFICIENCY", "EDS due to Tnx deficiency", "Classical-like EDS type 1", "Ehlers-Danlos syndrome, classic-like", "EHLERS-DANLOS SYNDROME, CLASSIC-LIKE", "classical-like Ehlers-Danlos syndrome", "Ehlers-Danlos syndrome classic-like 1", "Ehlers-Danlos syndrome, classic-like, 1", "Ehlers-Danlos syndrome classic-like type", "Ehlers-Danlos syndrome, classic-like type", "Classical-like Ehlers-Danlos syndrome type 1", "EHLERS-DANLOS SYNDROME DUE TO TENASCIN-X DEFICIENCY", "Ehlers-Danlos syndrome due to tenascin-X deficiency", "Ehlers-Danlos syndrome caused by tenascin-X deficiency", "Ehlers-Danlos-like syndrome due to tenascin-X deficiency", "Ehlers-Danlos syndrome due to tenascin-X deficiency (disorder)", "Ehlers-Danlos-like syndrome due to tenascin-X deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ehlers-Danlos syndrome due to tenascin-X deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0100423", "names": ["AML, SHP2 Gene Mutation", "AML, BPTP3 Gene Mutation", "AML, PTP2C Gene Mutation", "AML, SHP-2 Gene Mutation", "AML, PTP-1D Gene Mutation", "AML, PTPN11 gene mutation", "AML, SH-PTP2 Gene Mutation", "acute myeloid leukemia, PTPN11 gene mutation", "AML, Protein Tyrosine Phosphatase Non-Receptor Type 11 Gene Mutation", "AML, Protein Tyrosine Phosphatase, Non-Receptor Type 11 Gene Mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, PTPN11 gene mutation", "shortest_name_length": 23}
{"curie": "MONDO:0017485", "names": ["femoral agenesis/hypoplasia, bilateral", "femoral intercalary meromelia, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "femoral agenesis/hypoplasia, bilateral", "shortest_name_length": 38}
{"curie": "UMLS:C5206648", "names": ["Primary Peritoneal Transitional Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Peritoneal Transitional Cell Carcinoma", "shortest_name_length": 46}
{"curie": "MONDO:0003409", "names": ["disease colon", "colon disease", "colons disease", "disorder colon", "colon diseases", "colon; disease", "colon disorder", "Colon Disorders", "colonic disease", "colon disorders", "Colonic Disease", "Disease, Colonic", "of colon disease", "colonic disorder", "disease of colon", "colonic diseases", "Colonic Diseases", "Disease of colon", "disorder of colon", "Diseases, Colonic", "Disorder of colon", "colon disease or disorder", "disease (or disorder); colon", "disease or disorder of colon", "Disorder of colon (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colonic disorder", "shortest_name_length": 13}
{"curie": "MONDO:0006823", "names": ["47, XXY", "XXY male", "Klinefelter", "XXY trisomy", "xxy syndrome", "XXY syndrome", "XXY Syndrome", "XXY SYNDROME", "XXY; syndrome", "Syndrome, XXY", "XXY Syndromes", "syndrome; XXY", "Syndromes, XXY", "47,XXY syndrome", "47,XXY Syndrome", "KLINEFELTER DISEASE", "klinefelter disease", "klinefelter syndrome", "primary hypogonadism", "KLINEFELTER SYNDROME", "Klinefelter Syndrome", "Klinefelter syndrome", "Hypogonadism, primary", "klinefelters syndrome", "Syndrome, Klinefelter", "Klinefelters Syndrome", "Klinefelter Syndromes", "Klinefelter's Syndrome", "klinefelter's syndrome", "Klinefelter's syndrome", "KLINEFELTER'S SYNDROME", "Syndromes, Klinefelter", "intersex complex 47,XXY", "Xq Klinefelter syndrome", "47,XXY complex intersex", "complex intersex 47,XXY", "Syndrome, Klinefelter's", "chromosome XXY syndrome", "chromosome xxy syndrome", "klinefelter's syndromes", "klinefelter 's syndrome", "Klinefelter syndrome, XXY", "Klinefelter syndrome (KS)", "XXY Klinefelter's syndrome", "Klinefelter's Syndrome, XXY", "Klinefelter's syndrome, XXY", "Klinefelter's syndrome (XXY)", "hypogonadotropic hypogonadism", "Hypogonadotropic Hypogonadism", "seminiferous tubule dysgenesis", "karyotype; 47,XXY, Klinefelter", "hypogonadism; hypogonadotropic", "Klinefelter syndrome (disorder)", "Klinefelter-Reifenstein syndrome", "Klinefelter syndrome, unspecified", "complex intersex 47,XXY (diagnosis)", "Klinefelter's syndrome, unspecified", "XXY Syndrome (Klinefelter Syndrome)", "XXY syndrome (Klinefelter syndrome)", "Klinefelter syndrome karyotype 47,XXY", "chromosome; anomaly, sex, Klinefelter", "Klinefelter syndrome karyotype 47, XXY", "Klinefelter's syndrome, XXY (disorder)", "Klinefelter's syndrome karyotype 47 XXY", "Klinefelter's syndrome karyotype 47,XXY", "Klinefelter's syndrome (XXY) (diagnosis)", "Klinefelter-Reifenstein-Albright syndrome", "seminiferous tubule dysgenesis (diagnosis)", "Klinefelter syndrome karyotype 47,XXY (diagnosis)", "anomaly; chromosomes, chromosomal, sex, Klinefelter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Klinefelter syndrome", "shortest_name_length": 7}
{"curie": "UMLS:C2827403", "names": ["Anaplastic Astroblastoma", "Anaplastic Astroblastoma, MN1-Altered"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anaplastic Astroblastoma, MN1-Altered", "shortest_name_length": 24}
{"curie": "MONDO:0030462", "names": ["JBTS40", "JOUBERT SYNDROME 40", "Joubert syndrome 40"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome 40", "shortest_name_length": 6}
{"curie": "MONDO:0007318", "names": ["AHD", "AWS", "ALGS", "Alagille", "alagille syndrome", "Alagille syndrome", "Alagille Syndrome", "syndrome alagille", "ALAGILLE SYNDROME", "alagilles syndrome", "Syndrome, Alagille", "Alagilles Syndrome", "Alagille's Syndrome", "Alagille's syndrome", "Syndrome, Alagille's", "Watson Miller Syndrome", "Watson-Miller syndrome", "Syndrome, Watson Miller", "syndrome, Watson-Miller", "Alagille syndrome (AGS)", "Arteriohepatic Dysplasia", "ARTERIOHEPATIC DYSPLASIA", "Alagille-Watson Syndrome", "arteriohepatic dysplasia", "Arteriohepatic dysplasia", "Cardiovertebral syndrome", "Alagille Watson Syndrome", "alagille-watson syndrome", "Watson-Alagille syndrome", "Watson Alagille Syndrome", "Alagille-Watson syndrome", "ALAGILLE-WATSON SYNDROME", "Watson Alagille syndrome", "Cardiovertebral Syndrome", "cardiovertebral syndrome", "Syndrome, Watson Alagille", "Syndrome, Alagille Watson", "Syndrome, Alagille-Watson", "Dysplasia, Arteriohepatic", "Syndrome, Cardiovertebral", "Syndromic bile duct paucity", "syndromic bile duct paucity", "hepatic ductular hypoplasia", "Alagille syndrome (diagnosis)", "arteriohepatic dysplasia (AHD)", "Alagille-Watson syndrome (AWS)", "Arteriohepatic Dysplasia (AHD)", "Dysplasia, Arteriohepatic (AHD)", "paucity of interlobular bile ducts", "Arteriohepatic dysplasia (disorder)", "Hepatofacioneurocardiovertebral syndrome", "Hepatofacioneurocardiovertebral Syndrome", "Hepatic Ductular Hypoplasia, Syndromatic", "hepatofacioneurocardiovertebral syndrome", "HEPATIC DUCTULAR HYPOPLASIA, SYNDROMATIC", "cholestasis-peripheral pulmonary stenosis", "Syndrome, Hepatofacioneurocardiovertebral", "paucity of interlobular bile ducts (PILBD)", "CHOLESTASIS WITH PERIPHERAL PULMONARY STENOSIS", "Cholestasis with Peripheral Pulmonary Stenosis", "hepatic ductular hypoplasia-multiple malformations syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alagille syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C4688658", "names": ["Stage IIC Testicular Cancer", "Stage IIC Testicular Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIC Testicular Cancer AJCC v8", "shortest_name_length": 27}
{"curie": "UMLS:C1511055", "names": ["Basal Cell Ameloblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Basal Cell Ameloblastoma", "shortest_name_length": 24}
{"curie": "UMLS:C0341439", "names": ["chronic hepatic", "HEPATIC: CHRONIC", "Chronic hepatopathy", "Chronic liver disease", "chronic liver disease", "Chronic Liver Disease", "LIVER DISEASE CHRONIC", "chronic disease liver", "Chronic_Liver_Disease", "liver disease chronic", "chronic diseases liver", "Chronic liver disease (disorder)", "chronic liver disease (diagnosis)", "liver; disease (chronic) (organic)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic liver disease", "shortest_name_length": 15}
{"curie": "UMLS:C0860159", "names": ["Partial androgen resistance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Partial androgen resistance", "shortest_name_length": 27}
{"curie": "MONDO:0016322", "names": ["CTI", "NEHI", "NCHI", "chronic tachypnoe of infancy", "neuroendocrine cell hyperplasia of infancy", "Neuroendocrine cell hyperplasia of infancy", "Neuroendocrine Cell Hyperplasia of Infancy", "Neuroendocrine cell hyperplasia of infancy (disorder)", "neuroendocrine cell hyperplasia of infancy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuroendocrine cell hyperplasia of infancy", "shortest_name_length": 3}
{"curie": "MONDO:0001532", "names": ["capillariasis", "capillariosis", "Capillariosis", "Capillariasis", "Capillariases", "Capillariasis NOS", "Capillaria Infection", "Capillaria infection", "Infection, Capillaria", "Capillaria Infections", "infections, Capillaria", "Capillaria infection, NOS", "Capillaria infection (disorder)", "Capillaria infection (diagnosis)", "intestinal nematode infection capillaria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "capillariasis", "shortest_name_length": 13}
{"curie": "MONDO:0014415", "names": ["kallikrein, decreased urinary activity of", "Kallikrein, Decreased Urinary Activity of", "KALLIKREIN, DECREASED URINARY ACTIVITY OF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kallikrein, decreased urinary activity of", "shortest_name_length": 41}
{"curie": "MONDO:0010130", "names": ["DPD DEFICIENCY", "DPD Deficiency", "DPD deficiency", "DPYD DEFICIENCY", "Dpyd deficiency", "Deficiency, DPD", "DYPD deficiency", "DPYD Deficiency", "DPD Deficiencies", "Deficiencies, DPD", "thymine-uracilurea", "Thymine-Uracilurea", "Thymine-Uraciluria", "Familial Pyrimidemia", "Familial Pyrimidemias", "Pyrimidemia, Familial", "Familial Pyrimidinemia", "familial pyrimidinemia", "Fluorouracil poisoning", "Pyrimidemias, Familial", "Familial pyrimidinemia", "Pyrimidinemia, Familial", "PYRIMIDINEMIA, FAMILIAL", "pyrimidinemia, familial", "Familial Pyrimidinemias", "5-FLUOROURACIL TOXICITY", "Familial pyrimidinaemia", "5-fluorouracil toxicity", "familial pyrimidinaemia", "5-fluorouracil poisoning", "Pyrimidinemias, Familial", "5-@FLUOROURACIL TOXICITY", "Poisoning by fluorouracil", "5-fluorouracil intoxication", "toxicity from 5-fluorouracil", "Hereditary Thymine Uraciluria", "hereditary thymine-uraciluria", "Hereditary thymine-uraciluria", "Hereditary Thymine-Uraciluria", "THYMINE-URACILURIA, HEREDITARY", "thymine-Uraciluria, hereditary", "Hereditary Thymine-Uracilurias", "Thymine Uraciluria, Hereditary", "Thymine-Uraciluria, Hereditary", "Thymine-Uracilurias, Hereditary", "Poisoning caused by fluorouracil", "5-fluorouracil toxicity (diagnosis)", "Sensitivity to fluorouracil toxicity", "Dihydrouracil Dehydrogenase Deficiency", "dihydrouracil dehydrogenase deficiency", "Dihydrouracil Dehydrogenase deficiency", "Dihydrothymine dehydrogenase deficiency", "Dihydropyrimidine Dehydrogenase Deficiency", "DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY", "Dihydropyrimidine dehydrogenase deficiency", "dihydropyrimidine dehydrogenase deficiency", "Poisoning caused by fluorouracil (disorder)", "Dehydrogenase Deficiency, Dihydropyrimidine", "Deficiency, Dihydropyrimidine Dehydrogenase", "Dihydropyrimidine Dehydrogenase Deficiencies", "Dehydrogenase Deficiencies, Dihydropyrimidine", "Dihydrouracil dehydrogenase (NADP) deficiency", "Deficiencies, Dihydropyrimidine Dehydrogenase", "Reduced dihydropyrimidine dehydrogenase level", "Dihydrouracil dehydrogenase (NADP+) deficiency", "Dihydrouracil dehydrogenase (NADP^+^) deficiency", "DPD - dihydropyrimidine dehydrogenase deficiency", "Dihydropyrimidine dehydrogenase deficiency (disorder)", "dihydropyrimidine dehydrogenase deficiency (diagnosis)", "Dihydrouracil dehydrogenase (NADP<sup>+</sup>) deficiency", "Dihydrouracil dehydrogenase (nicotinamide adenine dinucleotide phosphate +) deficiency", "Dihydrouracil dehydrogenase (nicotinamide adenine dinucleotide phosphate ^+^) deficiency", "Dihydrouracil dehydrogenase (nicotinamide adenine dinucleotide phosphate <sup>+</sup>) deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dihydropyrimidine dehydrogenase deficiency", "shortest_name_length": 14}
{"curie": "UMLS:C1290332", "names": ["Throat ulcer", "ulcer; throat", "throat; ulcer", "ulcer; pharynx", "pharynx; ulcer", "Ulcer of pharynx", "PHARYNGEAL ULCERATION", "Pharyngeal ulceration", "Ulcer of pharynx (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ulcer of pharynx", "shortest_name_length": 12}
{"curie": "MONDO:0016661", "names": ["infantile onset panniculitis with uveitis and systemic granulomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile onset panniculitis with uveitis and systemic granulomatosis", "shortest_name_length": 69}
{"curie": "MONDO:0005697", "names": ["cns toxoplasmosis", "CNS TOXOPLASMOSIS", "brain toxoplasmosis", "toxoplasmosis cerebral", "Toxoplasmosis of brain", "Cerebral Toxoplasmosis", "cerebral toxoplasmosis", "Cerebral toxoplasmosis", "Toxoplasma encephalitis", "Toxoplasmoses, Cerebral", "Toxoplasmosis, Cerebral", "toxoplasma encephalitis", "Encephalitis toxoplasmal", "Toxoplasmal encephalitis", "toxoplasmosis encephalitis", "Toxoplasmosis encephalitis", "ENCEPHALITIS TOXOPLASMOSIS", "TE - Toxoplasma encephalitis", "Toxoplasma meningoencephalitis", "toxoplasma gondii encephalitis", "MENINGOENCEPHALITIS TOXOPLASMA", "toxoplasma meningoencephalitis", "Toxoplasma gondii encephalitis", "TOXOPLASMA MENINGOENCEPHALITIS", "Toxoplasma encephalitis (disorder)", "Acquired toxoplasmal meningoencephalitis", "meningoencephalitis due to toxoplasmosis", "Meningoencephalitis due to toxoplasmosis", "encephalitis due to acquired toxoplasmosis", "toxoplasma meningoencephalitis (diagnosis)", "Encephalitis due to acquired toxoplasmosis", "Meningoencephalitis due to acquired toxoplasmosis", "Meningoencephalitis due to acquired toxoplasmosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral toxoplasmosis", "shortest_name_length": 17}
{"curie": "MONDO:0021481", "names": ["benign submandibular gland tumor", "Benign Submandibular Gland Tumor", "benign submandibular gland neoplasm", "Benign Submandibular Gland Neoplasm", "Benign tumor of submandibular gland", "submandibular gland benign neoplasm", "benign tumor of submandibular gland", "Benign Tumor of Submandibular Gland", "Benign tumour of submandibular gland", "Benign neoplasm of submaxillary gland", "Benign Neoplasm of Submandibular Gland", "Benign neoplasm of submandibular gland", "benign neoplasm of submandibular gland", "benign tumor of the submandibular gland", "Benign Tumor of the Submandibular Gland", "Benign Neoplasm of the Submandibular Gland", "benign neoplasm of the submandibular gland", "Benign neoplasm of submaxillary gland (disorder)", "benign neoplasm of submandibular gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of submandibular gland", "shortest_name_length": 32}
{"curie": "UMLS:C4521828", "names": ["III", "Stage III Distal Bile Duct Cancer AJCC v8", "Stage III Distal Bile Duct Carcinoma AJCC v8", "Stage III Extrahepatic (Distal) Bile Duct Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Distal Bile Duct Cancer AJCC v8", "shortest_name_length": 3}
{"curie": "UMLS:C1336348", "names": ["Stage IVA Nasopharynx Carcinoma", "Stage IVA Nasopharyngeal Carcinoma", "Stage IVA Carcinoma of Nasopharynx", "Stage IVA Carcinoma of the Nasopharynx", "Stage IVA Nasopharyngeal Throat Cancer", "Stage IVA Nasopharyngeal Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Nasopharyngeal Carcinoma AJCC v7", "shortest_name_length": 31}
{"curie": "MONDO:0009151", "names": ["ED4", "OFC7", "CLEPD", "CLPED1", "OROFACIAL CLEFT 7", "Orofacial Cleft 7", "orofacial cleft 7", "Zlotogora syndrome", "Zlotogora-Ogur syndrome", "ZLOTOGORA-OGUR SYNDROME", "Zlotogora Ogur syndrome", "Ectodermal dysplasia type 4", "ectodermal dysplasia type 4", "ECTODERMAL DYSPLASIA, TYPE 4", "Ectodermal Dysplasia, Type 4", "ectodermal dysplasia, type 4", "margarita type of ectodermal dysplasia", "Bustos Simosa Pinto Cisternas syndrome", "Zlotogora Zilberman Tenenbaum syndrome", "Margarita type of ectodermal dysplasia", "cleft lip/palate-syndactyly-pili torti", "Bustos Simosa pinto Cisternas syndrome", "Zlotogora-Zilberman-Tenenbaum syndrome", "Autosomal recessive ectodermal dysplasia", "autosomal recessive ectodermal dysplasia", "Ectodermal dysplasia Margarita island type", "ectodermal dysplasia margarita island type", "Ectodermal Dysplasia, Margarita Island Type", "ECTODERMAL DYSPLASIA, MARGARITA ISLAND TYPE", "ectodermal dysplasia, margarita Island type", "Cleft Lip/Palate-Ectodermal Dysplasia Syndrome", "CLEFT LIP/PALATE-ECTODERMAL DYSPLASIA SYNDROME", "cleft lip/palate-ectodermal dysplasia syndrome", "Cleft lip-palate-ectodermal dysplasia syndrome", "cleft lip-palate-ectodermal dysplasia syndrome", "Cleft lip/palate-ectodermal dysplasia syndrome", "cleft lip/palate-syndactyly-pili torti syndrome", "Cleft lip/palate-syndactyly-pili torti syndrome", "syndactyly-ectodermal dysplasia-cleft/lip palate", "Syndactyly-ectodermal dysplasia-cleft/lip palate", "Cleft lip and palate with syndactyly and pili torti", "cleft lip with or without cleft palate, nonsyndromic, 7", "Cleft Lip with or without Cleft Palate, Nonsyndromic, 7", "CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 7", "Cleft lip and cleft palate with ectodermal dysplasia syndrome", "Cleft lip and cleft palate with ectodermal dysplasia syndrome (disorder)", "ECTODERMAL DYSPLASIA, CLEFT LIP AND PALATE, MENTAL RETARDATION, AND SYNDACTYLY", "Ectodermal dysplasia, cleft lip and palate, mental retardation, and syndactyly", "ectodermal dysplasia, cleft lip and palate, mental retardation, and syndactyly", "ectodermal dysplasia, cleft lip and palate, intellectual disability, and syndactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleft lip/palate-ectodermal dysplasia syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0014048", "names": ["CWS6", "Cowden syndrome 6", "COWDEN SYNDROME 6", "AKT1 Cowden disease", "Cowden syndrome type 6", "Cowden disease caused by mutation in AKT1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cowden syndrome 6", "shortest_name_length": 4}
{"curie": "UMLS:C1882974", "names": ["Salivary Gland Oncocytic Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Salivary Gland Oncocytic Carcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0032581", "names": ["NPHS18", "nephrotic syndrome type 18", "nephrotic syndrome, type 18", "NEPHROTIC SYNDROME, TYPE 18"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrotic syndrome, type 18", "shortest_name_length": 6}
{"curie": "UMLS:C0043145", "names": ["whiplash", "Whiplash", "WHIPLASH", "whiplash injury", "Whiplash injury", "Whiplash Injury", "injury; whiplash", "Injury, Whiplash", "whiplash; injury", "Whiplash Injuries", "Whiplash injuries", "whiplash injuries", "Injuries, Whiplash", "Injury;neck;whiplash", "whiplash neck injury", "Whiplash injury to neck", "Whiplash injury syndrome", "whiplash injury to the neck", "Whiplash injury to neck (disorder)", "Acceleration-deceleration injury of neck"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Whiplash Injuries", "shortest_name_length": 8}
{"curie": "UMLS:C0600272", "names": ["Morphine abuse", "morphine abuse", "Morphine Abuse", "Abuse, Morphine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Morphine Abuse", "shortest_name_length": 14}
{"curie": "MONDO:0001507", "names": ["epidemic vertigo", "Epidemic vertigo", "labyrinthitis viral", "LABYRINTHITIS VIRAL", "Viral labyrinthitis", "viral labyrinthitis", "Viral otitis interna", "Viruses labyrinthitis", "Viral labyrinthitis, NOS", "Viral otitis interna, NOS", "epidemic vertigo (finding)", "Viruses caused labyrinthitis", "Viral labyrinthitis syndrome", "Viral labyrinthitis (disorder)", "viral labyrinthitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "viral labyrinthitis", "shortest_name_length": 16}
{"curie": "MONDO:0020524", "names": ["primary parathyroid hyperplasia", "familial parathyroids hyperplasia", "hereditary parathyroids hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary parathyroid hyperplasia", "shortest_name_length": 31}
{"curie": "MONDO:0003532", "names": ["Papillary Breast Cancer", "Papillary breast cancer", "breast papillary carcinoma", "Papillary breast carcinoma", "papillary breast carcinoma", "Breast Papillary Carcinoma", "Papillary Breast Carcinoma", "Papillary Carcinoma of Breast", "papillary carcinoma of breast", "breast solid papillary carcinoma", "Breast Solid Papillary Carcinoma", "Solid Papillary Breast Carcinoma", "papillary carcinoma of the breast", "ductal papillary breast carcinoma", "Papillary carcinoma of the breast", "Papillary Carcinoma of the Breast", "papillary ductal breast carcinoma", "Solid Papillary Carcinoma of the Breast", "solid papillary carcinoma of the breast", "papillary carcinoma of breast (diagnosis)", "Papillary carcinoma of the breast (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast papillary carcinoma", "shortest_name_length": 23}
{"curie": "UMLS:C1141933", "names": ["Multi-organ disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Multi-organ disorder", "shortest_name_length": 20}
{"curie": "MONDO:0011092", "names": ["RIBBING DISEASE", "ribbing disease", "Ribbing disease", "Multiple diaphyseal sclerosis", "multiple diaphyseal sclerosis", "diaphyseal sclerosis, multiple", "Diaphyseal sclerosis, multiple", "DIAPHYSEAL SCLEROSIS, MULTIPLE", "hereditary multiple diaphyseal sclerosis", "Hereditary multiple diaphyseal sclerosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ribbing disease", "shortest_name_length": 15}
{"curie": "MONDO:0008040", "names": ["MST", "TMD", "TAM", "Mst", "transient leukemia", "leukemia, transient", "LEUKEMIA, TRANSIENT", "Leukemia, Transient", "TRANSIENT ABNORMAL MYELOPOIESIS", "Transient Abnormal Myelopoiesis", "transient abnormal myelopoiesis", "Transient abnormal myelopoiesis", "Transient leukemia of Down syndrome", "transient leukemia of Down syndrome", "transient myeloproliferative disease", "transient leurkemia of Down syndrome", "Transient myeloproliferative disease", "Transient leukaemia of Down syndrome", "Transient Abnormal Myelopoiesis (TAM)", "Transient myeloproliferative disorder", "Transient myeloproliferative syndrome", "Transient Myeloproliferative Disorder", "leukemia, transient, of Down syndrome", "transient myeloproliferative syndrome", "transient myeloproliferative disorder", "myeloproliferative syndrome, transient", "Myeloproliferative Syndrome, Transient", "MYELOPROLIFERATIVE SYNDROME, TRANSIENT", "Transient abnormal myelopoiesis (disorder)", "transient myeloproliferative syndrome (disease)", "Transient abnormal myelopoiesis (morphologic abnormality)", "Transient Abnormal Myelopoiesis Associated with Down Syndrome", "Transient abnormal myelopoiesis associated with Down syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transient myeloproliferative syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C5417745", "names": ["IJCN", "Inflamed Juvenile Conjunctival Nevus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Inflamed Juvenile Conjunctival Nevus", "shortest_name_length": 4}
{"curie": "UMLS:C4725028", "names": ["Unresectable Intrahepatic Cholangiocarcinoma", "Unresectable Intrahepatic Bile Duct Cancer (Cholangiocarcinoma)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Intrahepatic Cholangiocarcinoma", "shortest_name_length": 44}
{"curie": "UMLS:C2983723", "names": ["Laryngeal Cancer by AJCC v6 Stage", "Laryngeal Carcinoma by AJCC v6 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laryngeal Cancer by AJCC v6 Stage", "shortest_name_length": 33}
{"curie": "MONDO:0017069", "names": ["Myelomeningocele", "myelomeningocele", "Meningomyelocele", "meningomyelocele", "open spina bifida", "spina bifida, open", "Spina Bifida Aperta", "spina bifida aperta", "Spina bifida aperta", "Spina Bifida Cystica", "Spina bifida cystica", "spina bifida cystica", "spina bifida manifesta", "Spina Bifida Manifesta", "Spina bifida aperta (disorder)", "spina bifida (aperta)(cystica)", "Spina bifida aperta (diagnosis)", "Spina bifida cystica (diagnosis)", "congenital spinal anomaly spina bifida aperta", "congenital spinal anomaly spina bifida cystica"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spina bifida cystica", "shortest_name_length": 16}
{"curie": "UMLS:C1096714", "names": ["Infusion site infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infusion site infection", "shortest_name_length": 23}
{"curie": "UMLS:C4048303", "names": ["Osteoclastic Giant Cell-Rich Tumor of Bone", "Osteoclastic Giant Cell-Rich Tumor of the Bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Osteoclastic Giant Cell-Rich Tumor of Bone", "shortest_name_length": 42}
{"curie": "UMLS:C1696157", "names": ["Gastrointestinal stoma complication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal stoma complication", "shortest_name_length": 35}
{"curie": "MONDO:0013127", "names": ["ATD3", "SRPS3", "SRTD3", "SRPS1", "SRPS2B", "SRPS type 3", "SRPS type 1", "Verma-Naumoff syndrome", "VERMA-NAUMOFF SYNDROME", "Saldino-Noonan Syndrome", "Saldino-Noonan syndrome", "Saldino Noonan Syndrome", "Saldino Noonan syndrome", "SALDINO-NOONAN SYNDROME", "Short-rib syndrome, type I", "asphyxiating thoracic dystrophy 3", "ASPHYXIATING THORACIC DYSTROPHY 3", "Asphyxiating Thoracic Dystrophy 3", "Short rib-polydactyly syndrome type 3", "type I short rib polydactyly syndrome", "Short Rib Polydactyly Syndrome Type 1", "Short rib-polydactyly syndrome type 1", "Short Rib-Polydactyly Syndrome Type 1", "short rib-polydactyly syndrome type 3", "short rib-polydactyly syndrome type 1", "Short rib polydactyly syndrome type I", "Type I short rib polydactyly syndrome", "Short rib polydactyly syndrome type 1", "asphyxiating thoracic dystrophy type 3", "Short Rib-Polydactyly Syndrome, Type I", "short rib-polydactyly syndrome, type I", "Short Rib Polydactyly Syndrome, Type I", "SHORT RIB-POLYDACTYLY SYNDROME, TYPE I", "short rib-polydactyly syndrome type III", "Type III short rib polydactyly syndrome", "short rib-polydactyly syndrome, type 2B", "Short Rib-Polydactyly Syndrome, Type III", "SHORT RIB-POLYDACTYLY SYNDROME, TYPE III", "short rib-polydactyly syndrome, type IIB", "SHORT RIB-POLYDACTYLY SYNDROME, TYPE IIB", "Naumoff-type short rib polydactyly syndrome", "Verma-Naumoff short rib polydactyly syndrome", "Saldino Noonan short rib polydactyly syndrome", "Short rib polydactyly syndrome type I (disorder)", "Short rib-polydactyly syndrome, non-Majewski type", "polydactyly with neonatal chondrodystrophy type 1", "short rib polydactyly syndrome Verma Naumoff type", "Type III short rib polydactyly syndrome (disorder)", "Polydactyly with Neonatal Chondrodystrophy, Type 1", "POLYDACTYLY WITH NEONATAL CHONDRODYSTROPHY, TYPE I", "polydactyly with neonatal chondrodystrophy, type I", "Short rib-polydactyly syndrome, Verma-Naumoff type", "polydactyly with neonatal chondrodystrophy, type 3", "Short rib polydactyly syndrome Saldino Noonan type", "Polydactyly with neonatal chondrodystrophy, type 3", "Polydactyly With Neonatal Chondrodystrophy, Type I", "short rib-polydactyly syndrome Saldino-Noonan type", "Short Rib Polydactyly Syndrome, Saldino Noonan Type", "Short rib-polydactyly syndrome, Saldino-Noonan type", "polydactyly with neonatal chondrodystrophy type III", "Short Rib-Polydactyly Syndrome, Saldino-Noonan Type", "Polydactyly With Neonatal Chondrodystrophy, Type III", "polydactyly with neonatal chondrodystrophy, type III", "POLYDACTYLY WITH NEONATAL CHONDRODYSTROPHY, TYPE III", "Short-Rib Thoracic Dysplasia 3 with or without Polydactyly", "short-rib thoracic dysplasia 3 with or without polydactyly", "SHORT-RIB THORACIC DYSPLASIA 3 WITH OR WITHOUT POLYDACTYLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "asphyxiating thoracic dystrophy 3", "shortest_name_length": 4}
{"curie": "MONDO:0018380", "names": ["idiopathic AVN", "idiopathic avascular necrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic avascular necrosis", "shortest_name_length": 14}
{"curie": "MONDO:0005089", "names": ["SAR", "sarcoma", "Sarcoma", "SARCOMA", "Sarcomas", "Sarcoma NOS", "Sarcoma, NOS", "Soft part sarcoma", "SARCOMA, MALIGNANT", "Sarcoma (disorder)", "sarcoma, malignant", "Soft tissue sarcoma", "sarcoma (diagnosis)", "Soft Tissue Sarcoma", "Sarcoma, Soft Tissue", "Soft Tissue Sarcomas", "Sarcomas, Soft Tissue", "Malignant mesenchymal tumor", "Malignant soft tissue tumor", "Cancer of connective tissue", "Malignant soft tissue tumour", "Mesenchymal tumor, malignant", "Mesenchymal Tumor, Malignant", "Soft tissue tumor, malignant", "Malignant mesenchymal tumour", "mesenchymal tumor, malignant", "Mesenchymal tumour, malignant", "Soft tissue tumour, malignant", "sarcoma of soft tissue and bone", "Sarcoma of Soft Tissue and Bone", "Sarcoma, Not Otherwise Specified", "tumor of soft tissue and skeleton", "Sarcoma (morphologic abnormality)", "Malignant connective tissue tumor", "Malignant connective tissue tumour", "connective and soft tissue neoplasm", "Sarcoma of the Soft Tissue and Bone", "sarcoma of the soft tissue and bone", "Malignant neoplasm of other connective and soft tissue", "Malignant neoplasm of connective and other soft tissue", "Malignant neoplasm of connective and other soft tissues, NOS", "Malignant neoplasm of connective and other soft tissue, site unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sarcoma", "shortest_name_length": 3}
{"curie": "UMLS:C4525264", "names": ["Stage IIIA Intrahepatic Bile Duct Cancer", "stage IIIA intrahepatic bile duct cancer", "stage IIIA intrahepatic bile duct cancer AJCC v8", "Stage IIIA Intrahepatic Bile Duct Cancer AJCC v8", "stage IIIA intrahepatic bile duct carcinoma AJCC v8", "Stage IIIA Intrahepatic Bile Duct Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Intrahepatic Bile Duct Cancer AJCC v8", "shortest_name_length": 40}
{"curie": "MONDO:0001007", "names": ["chronic meningitis", "Chronic meningitis", "meningitis; chronic", "chronic; meningitis", "Chronic meningitis, NOS", "chronic meningitis (disease)", "meningitis (disease), chronic", "Chronic meningitis (disorder)", "chronic meningitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic meningitis", "shortest_name_length": 18}
{"curie": "MONDO:0014434", "names": ["BBS5", "BARDET-BIEDL SYNDROME 5", "Bardet-Biedl syndrome 5", "BBS5 Bardet-Biedl syndrome", "Bardet-Biedl syndrome type 5", "Bardet-Biedl syndrome caused by mutation in BBS5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bardet-Biedl syndrome 5", "shortest_name_length": 4}
{"curie": "MONDO:0003100", "names": ["Nerve Plexus Tumor", "nerve plexus tumor", "Nerve Plexus Tumors", "nerve plexus tumors", "Neural Plexus Tumors", "neural Plexus tumors", "neural plexus tumors", "Tumor of Nerve Plexus", "Nerve Plexus Neoplasm", "tumor of nerve plexus", "nerve plexus neoplasm", "Nerve Plexus Neoplasms", "nerve plexus neoplasms", "Neural Plexus Neoplasms", "neural plexus neoplasms", "neoplasm of nerve plexus", "Neoplasm of Nerve Plexus", "Tumor of the Nerve Plexus", "tumor of the nerve plexus", "neoplasm of the nerve plexus", "Neoplasm of the Nerve Plexus", "nerve plexus neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nerve plexus neoplasm", "shortest_name_length": 18}
{"curie": "MONDO:0023076", "names": ["EPF", "Classic EPF", "Ofuji disease", "Ofuji's disease", "Eosinophilic folliculitis", "eosinophilic folliculitis", "folliculitis pustular eosinophilic", "eosinophilic pustular folliculitis", "FOLLICULITIS EOSINOPHILIC PUSTULAR", "Eosinophilic pustular folliculitis", "Eosinophilic folliculitis, pustular", "eosinophilic folliculitis, pustular", "Classic eosinophilic pustular folliculitis", "Eosinophilic pustular folliculitis (disorder)", "Eosinophilic pustular folliculitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eosinophilic pustular folliculitis", "shortest_name_length": 3}
{"curie": "EFO:0009373", "names": ["edema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "edema", "shortest_name_length": 5}
{"curie": "MONDO:0009086", "names": ["GROLL-HIRSCHOWITZ SYNDROME", "Groll Hirschowitz syndrome", "Groll-Hirschowitz syndrome", "Groll-Hirschowitz Syndrome", "Deafness-small bowel diverticulosis-neuropathy syndrome", "deafness-small bowel diverticulosis-neuropathy syndrome", "Deafness, small bowel diverticulosis, neuropathy syndrome", "Hearing loss-small bowel diverticulosis-neuropathy syndrome", "Deafness, small bowel diverticulosis, neuropathy syndrome (disorder)", "nerve type deafness with mesenteric diverticula of small bowel and progressive sensory neuropathy", "deafness, nerve type, with mesenteric diverticula of small bowel and progressive sensory neuropathy", "DEAFNESS, NERVE TYPE, WITH MESENTERIC DIVERTICULA OF SMALL BOWEL AND PROGRESSIVE SENSORY NEUROPATHY", "Deafness, Nerve Type, with Mesenteric Diverticula of Small Bowel and Progressive Sensory Neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness-small bowel diverticulosis-neuropathy syndrome", "shortest_name_length": 26}
{"curie": "MONDO:0023659", "names": ["DEE96", "developmental and epileptic encephalopathy 96", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 96"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy 96", "shortest_name_length": 5}
{"curie": "MONDO:0019588", "names": ["EKVP1", "Deafness, Autosomal Recessive", "deafness, autosomal recessive", "DEAFNESS, AUTOSOMAL RECESSIVE", "hearing loss, autosomal recessive", "DEAFNESS, AUTOSOMAL RECESSIVE (disorder)", "autosomal recessive nonsyndromic deafness", "nonsyndromic deafness, autosomal recessive", "ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 1", "autosomal recessive nonsyndromic genetic deafness", "nonsyndromic genetic deafness, autosomal recessive", "deafness, neurosensory nonsyndromic recessive, DFN", "DEAFNESS, AUTOSOMAL DOMINANT, WITH PERIPHERAL NEUROPATHY", "autosomal recessive isolated neurosensory deafness type DFNB", "autosomal recessive isolated sensorineural deafness type DFNB", "autosomal recessive non-syndromic neurosensory deafness type DFNB", "autosomal recessive non-syndromic sensorineural deafness type DFNB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal recessive", "shortest_name_length": 5}
{"curie": "UMLS:C5448100", "names": ["Refractory Salivary Gland Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Salivary Gland Carcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C4520988", "names": ["Stage 0 Adenosquamous Lung Cancer", "Lung Adenosquamous Cell Carcinoma in situ", "Stage 0 Adenosquamous Cell Lung Carcinoma", "Stage 0 Adenosquamous Lung Carcinoma AJCC v6", "Adenosquamous Cell Carcinoma in situ of Lung", "Stage 0 Adenosquamous Cell Carcinoma of Lung", "Stage 0 Adenosquamous Lung Carcinoma AJCC v7", "Adenosquamous Cell Carcinoma in situ of the Lung", "Stage 0 Adenosquamous Cell Carcinoma of the Lung", "Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Lung Adenosquamous Carcinoma AJCC v6 and v7", "shortest_name_length": 33}
{"curie": "MONDO:0008619", "names": ["Rosenberg Lohr syndrome", "Rosenberg-Lohr syndrome", "ulna metaphyseal dysplasia syndrome", "ULNA METAPHYSEAL DYSPLASIA SYNDROME", "Ulna metaphyseal dysplasia syndrome", "metaphyseal chondroplasia Rosenberg type", "Metaphyseal chondroplasia Rosenberg type", "metaphyseal chondrodysplasia, Rosenberg type", "METAPHYSEAL CHONDRODYSPLASIA, ROSENBERG TYPE", "Metaphyseal Chondrodysplasia, Rosenberg Type", "Ulna metaphyseal dysplasia syndrome (disorder)", "hereditary bone dysplasia with characteristic bowing and thickening of the distal ulna", "Hereditary bone dysplasia with characteristic bowing and thickening of the distal ulna"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ulna metaphyseal dysplasia syndrome", "shortest_name_length": 23}
{"curie": "UMLS:C4764393", "names": ["Thoracic Nodule", "Chest Wall Nodule"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thoracic Nodule", "shortest_name_length": 15}
{"curie": "UMLS:C2826148", "names": ["t-MDS/MPN", "Therapy-Related Myelodysplastic/Myeloproliferative Disease", "Therapy-Related Myelodysplastic/Myeloproliferative Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Therapy-Related Myelodysplastic/Myeloproliferative Neoplasm", "shortest_name_length": 9}
{"curie": "UMLS:C0341751", "names": ["bladder necrosis", "Bladder necrosis", "bladder; necrosis", "necrosis; bladder", "Bladder necrosis (disorder)", "bladder necrosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder necrosis", "shortest_name_length": 16}
{"curie": "MONDO:0001160", "names": ["conversion disorder", "dissociative disease", "conversions disorder", "DISSOCIATIVE DISORDER", "disorder dissociative", "Disorder;dissociative", "Reaction dissociative", "Dissociative reaction", "Dissociative disorder", "DISSOCIATIVE REACTION", "Dissociative Reaction", "Dissociative Disorder", "dissociative reaction", "REACTION DISSOCIATIVE", "dissociative disorder", "Dissociation reaction", "reaction; dissociative", "dissociative; disorder", "dissociative; reaction", "Dissociative disorders", "disorder; dissociative", "dissociative reactions", "Reaction, Dissociative", "Dissociative Disorders", "Dissociative Reactions", "Disorder, Dissociative", "disorders dissociative", "dissociative disorders", "DISSOCIATIVE DISORDERS", "Reactions, Dissociative", "Disorders, Dissociative", "Dissociative disorder NOS", "Dissociative disorder, NOS", "Dissociative disorder (disorder)", "Unspecified dissociative disorder", "dissociative disorder, unspecified", "unspecified nonpsychotic mental disorder", "Unspecified nonpsychotic mental disorder", "MENTAL DISORDER UNSPECIFIED NONPSYCHOTIC", "Unspecified Nonpsychotic Mental Disorder", "Nonpsychotic mental disorder, unspecified", "Dissociative disorder or reaction, unspecified", "dissociative disorder, unspecified (diagnosis)", "unspecified nonpsychotic mental disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dissociative disorder", "shortest_name_length": 19}
{"curie": "UMLS:C3146267", "names": ["Stage II Esophageal Cancer", "Stage II Esophageal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Esophageal Cancer AJCC v7", "shortest_name_length": 26}
{"curie": "UMLS:C0349459", "names": ["CIN2", "cin 2", "CIN 2", "cin ii", "CIN II", "CERVICAL CANCER CIN II", "Moderate cervical dysplasia", "CERVICAL DYSPLASIA MODERATE", "dysplasia; cervix, moderate", "moderate cervical dysplasia", "Moderate dysplasia of cervix", "dysplasia of cervix (uteri) moderate", "moderate cervical dysplasia (CIN II)", "Cervical intraepithelial neoplasia II", "cervical intra-epithelial neoplasm ii", "moderate cervical dysplasia (diagnosis)", "Moderate Squamous Dysplasia of the Cervix", "cervical intraepithelial neoplasia grade 2", "Cervical intraepithelial neoplasia grade 2", "Cervical intraepithelial neoplasia grade II", "cervix; intraepithelial neoplasia, grade II", "CIN 2 - Cervical intraepithelial neoplasia 2", "neoplasia; intraepithelial, cervix, grade II", "Cervical Squamous Intraepithelial Neoplasia 2", "cervical squamous intraepithelial neoplasia 2", "CIN II (grade 2 cervical intraepithelial neoplasia)", "Cervical intraepithelial neoplasia grade 2 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical intraepithelial neoplasia grade 2", "shortest_name_length": 4}
{"curie": "MONDO:0035665", "names": ["NMOSD without anti-MOG antibodies and without anti-AQP4 antibodies", "neuromyelitis optica spectrum disorder without anti-MOG and without anti-AQP4 antibodies", "Neuromyelitis optica spectrum disorder without anti-Myelin oligodendrocyte glycoprotein and without anti-Aquaporin-4 antibodies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuromyelitis optica spectrum disorder without anti-MOG and without anti-AQP4 antibodies", "shortest_name_length": 66}
{"curie": "UMLS:C1336324", "names": ["Stage II Supradiaphragmatic Nodular Lymphocyte Predominant Hodgkin Lymphoma", "Stage II Supradiaphragmatic Nodular Lymphocyte Predominant Hodgkin's Lymphoma", "Stage II Supradiaphragmatic Hodgkin Lymphoma Nodular Lymphocyte Predominant Type", "Stage II Supradiaphragmatic Hodgkin's Disease Nodular Lymphocyte Predominance Type", "Stage II Supradiaphragmatic Hodgkin's Lymphoma Nodular Lymphocyte Predominant Type", "Stage II Hodgkin's Disease Nodular Lymphocyte Predominance Type above the Diaphragm", "Stage II Hodgkin's Lymphoma Nodular Lymphocyte Predominance Type above the Diaphragm", "Ann Arbor Stage II Supradiaphragmatic Nodular Lymphocyte Predominant Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage II Supradiaphragmatic Nodular Lymphocyte Predominant Hodgkin Lymphoma", "shortest_name_length": 75}
{"curie": "MONDO:0011743", "names": ["AD4", "Ad4", "Alzheimer disease-4", "ALZHEIMER DISEASE 4", "Alzheimer disease 4", "Alzheimer's Disease 4", "Alzheimer's disease 4", "Alzheimer disease type 4", "Alzheimer's disease type 4", "Alzheimer disease, familial4", "Alzheimer Disease, Familial, 4", "Alzheimer disease, familial, 4", "ALZHEIMER DISEASE, FAMILIAL, 4", "Alzheimer disease familial type 4", "Alzheimer's disease 4, early onset", "Familial Alzheimer Disease, Type 4", "familial Alzheimer disease, type 4", "Alzheimer disease, familial, type 4", "familial Alzheimer's disease, type 4", "Familial Alzheimer's Disease, Type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alzheimer disease 4", "shortest_name_length": 3}
{"curie": "MONDO:0021108", "names": ["Meningitis", "MENINGITIS", "meningitis", "Meningitides", "meningitides", "Meningitis NOS", "meningitis NOS", "Meningitis, NOS", "meninx inflammation", "meningitis (disease)", "Meningitis (disorder)", "inflammation of meninx", "meningitis (diagnosis)", "Meningococcal Infection", "Meningitis, unspecified", "Inflammation of meninges", "infection; brain, membranes", "Meningitis of unspecified cause"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "meningitis", "shortest_name_length": 10}
{"curie": "UMLS:C3665848", "names": ["Hypothalamic pituitary adrenal axis suppression"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypothalamic pituitary adrenal axis suppression", "shortest_name_length": 47}
{"curie": "MONDO:0021512", "names": ["benign thymic tumor", "Benign Thymic Tumor", "Benign Thymus Tumor", "benign Thymus tumor", "benign tumor of Thymus", "Benign Tumor of Thymus", "Benign tumor of thymus", "benign thymic neoplasm", "benign thymus neoplasm", "thymus benign neoplasm", "benign tumor of thymus", "Benign Thymic Neoplasm", "Benign Thymus Neoplasm", "benign Thymus neoplasm", "Benign tumour of thymus", "Benign Neoplasm of Thymus", "Benign neoplasm of thymus", "benign neoplasm of thymus", "Benign Tumor of the Thymus", "benign tumor of the Thymus", "Benign Neoplasm of the Thymus", "benign neoplasm of the Thymus", "Benign neoplasm of thymus (disorder)", "benign neoplasm of thymus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of thymus", "shortest_name_length": 19}
{"curie": "UMLS:C4527164", "names": ["Stage IA Cutaneous (Skin) Melanoma", "Clinical Stage IA Cutaneous Melanoma AJCC v8", "Clinical Stage IA Melanoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage IA Cutaneous Melanoma AJCC v8", "shortest_name_length": 34}
{"curie": "MONDO:0015101", "names": ["Marin-Amat syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Marin-Amat syndrome", "shortest_name_length": 19}
{"curie": "UMLS:C0235955", "names": ["DERMATITIS HEMORRHAGIC", "Dermatitis hemorrhagic", "Dermatitis haemorrhagic", "DERMATITIS HAEMORRHAGIC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dermatitis haemorrhagic", "shortest_name_length": 22}
{"curie": "UMLS:C5446660", "names": ["Breast Neuroendocrine Tumor G2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Neuroendocrine Tumor G2", "shortest_name_length": 30}
{"curie": "MONDO:0008166", "names": ["Ovalocytosis, Hereditary Hemolytic, with Defective Erythropoiesis", "OVALOCYTOSIS, HEREDITARY HEMOLYTIC, WITH DEFECTIVE ERYTHROPOIESIS", "ovalocytosis, hereditary hemolytic, with defective erythropoiesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovalocytosis, hereditary hemolytic, with defective erythropoiesis", "shortest_name_length": 65}
{"curie": "MONDO:0022618", "names": ["BMS-3", "burning mouth syndrome type 3", "Type 3 burning mouth syndrome", "type 3 burning mouth syndrome", "Burning mouth syndrome- Type 3", "Psychiatric disorders coexisting with burning mouth syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "burning mouth syndrome type 3", "shortest_name_length": 5}
{"curie": "MONDO:0019474", "names": ["HSTCL", "hepatosplenic T-cell lymphoma", "Hepatosplenic T-Cell Lymphoma", "Hepatosplenic T-cell lymphoma", "Hepatosplenic gamma-delta cell lymphoma", "Hepatosplenic T-cell lymphoma (disorder)", "Hepatosplenic gamma/Delta T-cell lymphoma", "Hepatosplenic gamma-delta T-cell lymphoma", "hepatosplenic T-cell lymphoma (diagnosis)", "Hepatosplenic Gamma/Delta T-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatosplenic T-cell lymphoma", "shortest_name_length": 5}
{"curie": "UMLS:C0018200", "names": ["Respiratory Tract Granuloma", "Respiratory Tract Granulomas", "Respiratory System Granuloma", "Granuloma, Respiratory Tract", "Granuloma, Respiratory System", "Respiratory System Granulomas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Granuloma, Respiratory Tract", "shortest_name_length": 27}
{"curie": "UMLS:C0085663", "names": ["PLASMOCYTOSIS", "plasmocytosis", "plasmacytosis", "PLASMACYTOSIS", "Plasmacytosis", "Plasmocytosis", "Plasmacytosis, NOS", "Hyperplasia, plasma cell", "Plasmacytosis (disorder)", "plasmacytosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Plasmacytosis", "shortest_name_length": 13}
{"curie": "UMLS:C3831153", "names": ["Central Hyperthyroidism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Hyperthyroidism", "shortest_name_length": 23}
{"curie": "MONDO:0020334", "names": ["MCL", "SMMCL", "Mast Cell Leukemia", "Mast cell leukemia", "mast-cell leukemia", "MAST CELL LEUKEMIA", "mast cell leukemia", "Mast-Cell Leukemia", "leukemia; mast cell", "Leukemia, Mast-Cell", "Mastocytic leukemia", "Mast-Cell Leukemias", "mast cell; leukemia", "Mast cell leukaemia", "Leukemia, Mast Cell", "mast cell leukaemia", "Leukemias, Mast-Cell", "Mastocytic leukaemia", "[M]Mast cell leukemia", "Mast cell leukemia NOS", "[M]Mast cell leukaemia", "aleukemic mast cell leukemia", "Mast cell leukemia (disorder)", "Mast cell leukemia (clinical)", "LEUKEMIA, MAST CELL, MALIGNANT", "Mast cell leukaemia (clinical)", "mast cell leukemia (diagnosis)", "Noncutaneous systemic mastocytosis", "Mast cell leukemia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mast cell leukemia", "shortest_name_length": 3}
{"curie": "MONDO:0000727", "names": ["scapuloperoneal myopathy", "Scapuloperoneal myopathy", "myopathy, scapuloperoneal", "Myopathy, scapuloperoneal", "Scapuloperoneal syndrome, myopathic type", "scapuloperoneal syndrome, myopathic type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scapuloperoneal myopathy", "shortest_name_length": 24}
{"curie": "MONDO:0004642", "names": ["tonsillar pillar cancer", "Malignant tumor of tonsillar pillar", "malignant tumor of tonsillar pillar", "Malignant neoplasm of faucial pillar", "malignant tumor of tonsillar pillars", "malignant tumour of tonsillar pillar", "Malignant tumour of tonsillar pillar", "malignant neoplasm of faucial pillars", "Malignant neoplasm of tonsillar pillar", "malignant neoplasm of tonsillar pillar", "Malignant neoplasm of tonsillar pillars", "malignant neoplasm of tonsillar pillars", "Malignant tumor of palatopharyngeal arch", "Malignant tumor of pharyngopalatine arch", "Malignant tumour of pharyngopalatine arch", "Malignant tumour of palatopharyngeal arch", "malignant neoplasm of palatopharyngeal arch", "Malignant neoplasm of palatopharyngeal arch", "Malignant tumor of posterior faucial pillar", "Malignant tumour of posterior faucial pillar", "Malignant tumor of posterior tonsillar pillar", "Malignant tumour of posterior tonsillar pillar", "Malignant tumor of tonsillar pillar (disorder)", "malignant neoplasm of faucial pillars (diagnosis)", "malignant neoplasm of tonsillar pillars, posterior", "Malignant neoplasm of tonsillar pillars, posterior", "malignant neoplasm of tonsillar pillars (diagnosis)", "malignant neoplasm of palatopharyngeal arch (diagnosis)", "oropharyngeal neoplasm tonsillar pillars, malignant faucial", "Malignant neoplasm of tonsillar pillar (anterior)(posterior)", "Malignant neoplasm of tonsillar pillar (anterior) (posterior)", "Malignant neoplasm of tonsillar pillars (anterior) (posterior)", "oropharyngeal neoplasm tonsillar pillars, malignant palatopharyngeal arch"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tonsillar pillar cancer", "shortest_name_length": 23}
{"curie": "MONDO:0014120", "names": ["MDDGA13", "congenital muscular dystrophy-dystroglycanopathy type A13", "Walker-Warburg syndrome or muscle-eye-brain disease, B4GNT1-related", "Walker-Warburg syndrome or muscle-eye-brain disease, B3GNT1-related", "WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, B3GNT1-RELATED", "Walker-Warburg syndrome or muscle-eye-brain disease, B3Gnt1-related", "congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A13", "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A13", "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A13", "shortest_name_length": 7}
{"curie": "MONDO:0017015", "names": ["child", "primary ILD specific to childhood", "children's interstitial lung disease", "primary interstitial lung disease specific to childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary interstitial lung disease specific to childhood", "shortest_name_length": 5}
{"curie": "MONDO:0017492", "names": ["fibular hemimelia, unilateral", "fibular longitudinal meromelia, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibular hemimelia, unilateral", "shortest_name_length": 29}
{"curie": "MONDO:0042981", "names": ["AS", "as", "aorta stenosis", "stenose aortic", "stenosis aorta", "aortic stenosis", "AORTIC STENOSIS", "Aortic Stenosis", "stenosis aortic", "Aortic stenosis", "Stenosis;aortic", "Stenosis, Aortic", "Stenoses, Aortic", "stenosis - aortic", "AS - Aortic stenosis", "Aortic Valve Stenosis", "Aortic Valve Stenoses", "AORTIC VALVE STENOSIS", "Stenosis aortic valve", "stenosed aortic valve", "Aortic valve stenosis", "Stenosed aortic valve", "STENOSIS AORTIC VALVE", "aortic valve stenosis", "stenosis; aortic valve", "Valve Stenoses, Aortic", "Stenoses, Aortic Valve", "Stenosis, Aortic Valve", "Aortic valve--Stenosis", "aorta; stenosis, valve", "aortic valve; stenosis", "Valve Stenosis, Aortic", "Aortic (valve) stenosis", "aortic valve; stricture", "AORTIC VALVULAR STENOSIS", "valvular aortic stenosis", "Stenosis of aortic valve", "Valvular aortic stenosis", "aortic valvular stenosis", "Narrowing of aortic valve", "rheumatic aortic stenosis", "Stenosis;aortic;rheumatic", "Rheumatic aortic stenosis", "Aortic valve stenosis, NOS", "obstruction; aortic, rheumatic", "Rheumatic aortic valve stenosis", "rheumatic aortic valve stenosis", "Aortic valve stenosis (disorder)", "stenosis; aortic valve, rheumatic", "Rheumatic aortic valve obstruction", "aortic valvular stenosis (diagnosis)", "Rheumatic aortic stenosis (disorder)", "rheumatic aortic stenosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic valve stenosis", "shortest_name_length": 2}
{"curie": "MONDO:0001366", "names": ["Splenic sequestration", "splenic sequestration", "splenic sequestration (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "splenic sequestration", "shortest_name_length": 21}
{"curie": "MONDO:0015788", "names": ["symptomatic form of hemophilia B in female carriers"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "symptomatic form of hemophilia B in female carriers", "shortest_name_length": 51}
{"curie": "MONDO:0021527", "names": ["benign meninges tumor", "Benign Meninges Tumor", "benign meningeal tumor", "Benign Meningeal Tumor", "benign meningeal tumors", "Benign Meningeal Tumors", "benign tumor of meninges", "Meningeal Tumors, Benign", "Neoplasm benign;meninges", "Benign tumor of meninges", "benign meninges neoplasm", "meningeal tumors, benign", "Benign Tumor of Meninges", "Benign Meninges Neoplasm", "Benign Meningeal Neoplasm", "Benign tumour of meninges", "Benign meningeal neoplasm", "benign meningeal neoplasm", "Meningeal Neoplasm, Benign", "Neoplasm, Benign Meningeal", "benign meningeal neoplasms", "Benign Meningeal Neoplasms", "Benign Neoplasm of Meninges", "Neoplasms, Benign Meningeal", "benign neoplasm of meninges", "Meningeal Neoplasms, Benign", "Benign neoplasm of meninges", "Benign Neoplasms of Meninges", "Benign Tumor of the Meninges", "benign tumor of the meninges", "benign neoplasms of meninges", "benign neoplasm of the meninges", "Benign neoplasm of meninges NOS", "Benign Neoplasm of the Meninges", "benign neoplasms of the meninges", "Benign Neoplasms of the Meninges", "meningeal cluster benign neoplasm", "Benign neoplasm of meninges (disorder)", "benign neoplasm of meninges (diagnosis)", "Benign neoplasm of meninges, unspecified", "Benign meningeal neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of meninges", "shortest_name_length": 21}
{"curie": "MONDO:0036482", "names": ["RP81", "RETINITIS PIGMENTOSA 81", "retinitis pigmentosa 81"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 81", "shortest_name_length": 4}
{"curie": "MONDO:0034092", "names": ["optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome", "shortest_name_length": 78}
{"curie": "MONDO:0007164", "names": ["SPAX1", "spastic ataxia 1", "spastic ataxia type 1", "SPASTIC ATAXIA 1, AUTOSOMAL DOMINANT", "spastic ataxia 1, autosomal dominant", "ATAXIA, SPASTIC, 1, AUTOSOMAL DOMINANT", "Ataxia, Spastic, 1, Autosomal Dominant", "VAMP1 autosomal dominant spastic ataxia", "Autosomal dominant spastic ataxia type 1", "autosomal dominant spastic ataxia type 1", "SPAX1 - autosomal dominant spastic ataxia type 1", "Autosomal dominant spastic ataxia type 1 (disorder)", "autosomal dominant spastic ataxia caused by mutation in VAMP1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic ataxia 1", "shortest_name_length": 5}
{"curie": "MONDO:0013447", "names": ["RP48", "retinitis pigmentosa 48", "RETINITIS PIGMENTOSA 48", "GUCA1B retinitis pigmentosa", "retinitis pigmentosa type 48", "retinitis pigmentosa caused by mutation in GUCA1B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 48", "shortest_name_length": 4}
{"curie": "MONDO:0009796", "names": ["GACR", "HOGA", "hoga", "Ornithinemia", "ornithinemia", "gyrate atrophy", "OKT DEFICIENCY", "Oat deficiency", "OKT Deficiency", "OAT deficiency", "Gyrate Atrophy", "Okt deficiency", "GYRATE ATROPHY", "Gyrate atrophy", "OKT deficiency", "OAT Deficiency", "OAT DEFICIENCY", "Atrophy, Gyrate", "Deficiency, OKT", "Deficiency, OAT", "hyperornithinemia", "Hyperornithinemia", "Hyperornithinaemia", "Fuchs gyrate atrophy", "Hyperornithinemia, NOS", "Hyperornithinaemia, NOS", "Gyrate atrophy (disorder)", "High blood ornithine levels", "gyrate atrophy of the retina", "Girate atrophy of the retina", "Hyperornithinemia (disorder)", "hyperornithinemia (diagnosis)", "gyrate atrophy of retina choroid", "Ornithinemia with Gyrate Atrophy", "Ornithinemia with gyrate atrophy", "Ornithinaemia with gyrate atrophy", "Gyrate Atrophy of Choroid and Retina", "gyrate atrophy of choroid and retina", "Gyrate atrophy of choroid and retina", "GYRATE ATROPHY OF CHOROID AND RETINA", "Ornithine Aminotransferase Deficiency", "Ornithine aminotransferase deficiency", "ornithine aminotransferase deficiency", "ORNITHINE AMINOTRANSFERASE DEFICIENCY", "Deficiency, Ornithine Aminotransferase", "Gyrate Atrophy of the Choroid and Retina", "Gyrate atrophy of the choroid and retina", "Ornithine ketoacid transaminase deficiency", "Gyrate atrophy of the choroid and/or retina", "Ornithine-delta-aminotransferase deficiency", "ornithine-Delta-aminotransferase deficiency", "Ornithine Delta Aminotransferase Deficiency", "Ornithine-Delta-Aminotransferase Deficiency", "gyrate atrophy of the choroid and/or retina", "ORNITHINE-DELTA-AMINOTRANSFERASE DEFICIENCY", "Deficiency, Ornithine-Delta-Aminotransferase", "Ornithine oxoacidaminotransferase deficiency", "Fuchs atrophia gyrata chorioideae et retinae", "Fuchs gyrate atrophy of the choroid and retina", "Ornithine oxo-acid aminotransferase deficiency", "ornithine ketoacid aminotransferase deficiency", "Ornithine Ketoacid Aminotransferase Deficiency", "ORNITHINE KETO ACID AMINOTRANSFERASE DEFICIENCY", "Ornithine Keto Acid Aminotransferase Deficiency", "ornithine Keto acid aminotransferase deficiency", "Deficiency of ornithine-oxo-acid aminotransferase", "OAT - Ornithine oxo-acid aminotransferase deficiency", "Ornithine-oxo-acid amino acid transferase deficiency", "Ornithine oxo-acid aminotransferase deficiency (disorder)", "hyperornithinemia with gyrate atrophy of choroid and retina", "Hyperornithinemia with Gyrate Atrophy of Choroid and Retina", "HYPERORNITHINEMIA WITH GYRATE ATROPHY OF CHOROID AND RETINA", "Hyperornithinemia-gyrate atrophy of choroid and retina syndrome", "hyperornithinemia-gyrate atrophy of choroid and retina syndrome", "gyrate atrophy of choroid and retina with or without ornithinemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ornithine aminotransferase deficiency", "shortest_name_length": 4}
{"curie": "UMLS:C5206819", "names": ["Metastatic Malignant Colorectal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Malignant Colorectal Neoplasm", "shortest_name_length": 40}
{"curie": "UMLS:C0341505", "names": ["Chemical Peritonitis", "Chemical peritonitis", "peritonitis; chemical", "chemicals; peritonitis", "Chemical peritonitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chemical peritonitis", "shortest_name_length": 20}
{"curie": "MONDO:0009473", "names": ["Kawashima syndrome", "Isotretinoin-like syndrome", "isotretinoin-like syndrome", "MICROTIA-AORTIC ARCH SYNDROME", "microtia-aortic Arch syndrome", "Microtia aortic arch syndrome", "microtia-aortic arch syndrome", "microtia aortic arch syndrome", "Microtia-aortic arch syndrome", "Isotretinoin teratogen syndrome", "ISOTRETINOIN EMBRYOPATHY-LIKE SYNDROME", "ISOTRETINOIN embryopathy-like syndrome", "Isotretinoin embryopathy-like syndrome", "Isotretinoin embryopathy like syndrome", "Syndrome of microtia and aortic arch anomalies", "syndrome of microtia and aortic arch anomalies", "Isotretinoin embryopathy-like syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isotretinoin-like syndrome", "shortest_name_length": 18}
{"curie": "MONDO:0008962", "names": ["GS1", "Griscelli disease type 1", "Griscelli syndrome type 1", "Griscelli syndrome, type 1", "GRISCELLI SYNDROME, TYPE 1", "Griscelli Syndrome, Type 1", "Griscelli-Prunieras syndrome type 1", "Griscelli-Pruniéras syndrome type 1", "Griscelli-PruniC)ras syndrome type 1", "GRISCELLI SYNDROME WITH NEUROLOGIC IMPAIRMENT", "Griscelli syndrome with neurologic impairment", "hypopigmentation-neurologic impairment syndrome", "Griscelli syndrome with neurological impairment", "Hypopigmentation-neurologic impairment syndrome", "Hypopigmentation-immunodeficiency disease type 1", "Griscelli syndrome, cutaneous and neurologic type", "GRISCELLI SYNDROME, CUTANEOUS AND NEUROLOGIC TYPE", "Griscelli syndrome, cutaneous and neurological type", "Hypopigmentation-immunodeficiency disease type 1 (disorder)", "PARTIAL ALBINISM AND PRIMARY NEUROLOGIC DISEASE WITHOUT HEMOPHAGOCYTIC SYNDROME", "partial albinism and primary neurologic disease without hemophagocytic syndrome", "Partial albinism and primary neurologic disease without hemophagocytic syndrome", "pigmentary dilution of the skin and hair, the presence of large clumps of pigment in hair shafts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Griscelli syndrome type 1", "shortest_name_length": 3}
{"curie": "MONDO:0010906", "names": ["CHCL", "OFC11", "OROFACIAL CLEFT 11", "Orofacial Cleft 11", "orofacial cleft 11", "BMP4 orofacial cleft", "orofacial cleft type 11", "CONGENITAL HEALED CLEFT LIP", "Congenital Healed Cleft Lip", "congenital Healed cleft lip", "cleft Lip, congenital Healed", "Cleft Lip, Congenital Healed", "CLEFT LIP, CONGENITAL HEALED", "orofacial cleft caused by mutation in BMP4", "nonsyndromic cleft lip with or without cleft palate 11", "Cleft Lip with or without Cleft Palate, Nonsyndromic, 11", "cleft lip with or without cleft palate, nonsyndromic, 11", "CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orofacial cleft 11", "shortest_name_length": 4}
{"curie": "MONDO:0007588", "names": ["Char-Douglas-Dungan syndrome", "extrasystoles-short stature-hyperpigmentation-microcephaly syndrome", "Extrasystoles, Multiform Ventricular, with Short Stature, Hyperpigmentation and Microcephaly", "extrasystoles, multiform ventricular, with short stature, hyperpigmentation and microcephaly", "EXTRASYSTOLES, MULTIFORM VENTRICULAR, WITH SHORT STATURE, HYPERPIGMENTATION AND MICROCEPHALY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extrasystoles-short stature-hyperpigmentation-microcephaly syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0009137", "names": ["Dysmyelination With Jaundice", "DYSMYELINATION WITH JAUNDICE", "dysmyelination with jaundice"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dysmyelination with jaundice", "shortest_name_length": 28}
{"curie": "MONDO:0011288", "names": ["spastic paraplegia, optic atrophy, microcephaly, and XY SEX reversal", "Spastic Paraplegia, Optic Atrophy, Microcephaly, And Xy Sex Reversal", "SPASTIC PARAPLEGIA, OPTIC ATROPHY, MICROCEPHALY, AND XY SEX REVERSAL", "spastic paraplegia, optic atrophy, microcephaly, and 10Y sex reversal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic paraplegia, optic atrophy, microcephaly, and 10Y sex reversal", "shortest_name_length": 68}
{"curie": "UMLS:C1881600", "names": ["Malignant Vipoma", "Vipoma, malignant", "Vipoma, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Vipoma", "shortest_name_length": 16}
{"curie": "UMLS:C0543793", "names": ["RENAL DISEASE CONGENITAL", "congenital renal disorder", "Congenital renal disorder", "congenital renal disorders", "congenital kidney disorder", "Renal disorders congenital", "congenital disorders kidney", "Congenital kidney disease or syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital renal disorder", "shortest_name_length": 24}
{"curie": "MONDO:0004714", "names": ["atrophic muscular disease", "Atrophic Muscular Disorder", "atrophic muscular disorder", "Atrophic Muscular Disorders", "Muscular Disorder, Atrophic", "Disorder, Atrophic Muscular", "Muscular Disorders, Atrophic", "Disorders, Atrophic Muscular"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrophic muscular disease", "shortest_name_length": 25}
{"curie": "MONDO:0008327", "names": ["XFS", "XFG", "PEXG", "PEXS", "Glaucoma Capsulare", "capsular; glaucoma", "GLAUCOMA CAPSULARE", "Glaucoma capsulare", "glaucoma; capsular", "Exfoliation Glaucoma", "Exfoliative Syndrome", "Exfoliation Syndrome", "Exfoliation syndrome", "EXFOLIATION GLAUCOMA", "exfoliation syndrome", "EXFOLIATION SYNDROME", "Exfoliation glaucoma", "Exfoliation Syndromes", "Exfoliative Syndromes", "Syndrome, Exfoliative", "Syndrome, Exfoliation", "Syndromes, Exfoliative", "Syndromes, Exfoliation", "PEX - Pseudoexfoliation", "Pseudoexfoliation Syndrome", "pseudoexfoliation glaucoma", "Pseudoexfoliation syndrome", "Pseudoexfoliation glaucoma", "PSEUDOEXFOLIATION SYNDROME", "pseudoexfoliation syndrome", "PSEUDOEXFOLIATION GLAUCOMA", "pseudo exfoliation syndrome", "Pseudo-Exfoliation Syndrome", "Syndrome, Pseudoexfoliation", "Pseudo Exfoliation Syndrome", "Pseudoexfoliation Syndromes", "Syndromes, Pseudoexfoliation", "Pseudo-Exfoliation Syndromes", "Syndrome, Pseudo-Exfoliation", "Capsular exfoliation syndrome", "PSEUDOEXFOLIATION OF THE LENS", "Pseudoexfoliation Of The Lens", "Syndromes, Pseudo-Exfoliation", "Pseudoexfoliation lens capsule", "PSEUDOEXFOLIATION, LENS CAPSULE", "Pseudoexfoliation of lens capsule", "pseudoexfoliation, capsule; capsule", "Pseudoexfoliation glaucoma (disorder)", "pseudoexfoliation of the lens capsule", "PXF - Pseudoexfoliation of lens capsule", "capsule (lens); pseudoexfoliation, capsule", "Pseudoexfoliation of lens capsule (disorder)", "pseudoexfoliation of the lens capsule (diagnosis)", "Secondary open-angle glaucoma with pseudoexfoliation", "lens-induced open-angle glaucoma with pseudoexfoliation", "lens-induced open-angle glaucoma with pseudoexfoliation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exfoliation syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C3272608", "names": ["Colorectal Large Cell Neuroendocrine Carcinoma", "Large Intestinal Large Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Large Cell Neuroendocrine Carcinoma", "shortest_name_length": 46}
{"curie": "UMLS:C5419784", "names": ["Colon Conventional Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colon Conventional Adenoma", "shortest_name_length": 26}
{"curie": "UMLS:C0155668", "names": ["previous MI", "Healed coronary", "PAST HEART ATTACK", "prior heart attack", "Myocardial infarction old", "old myocardial infarction", "Infarction;myocardial;old", "Old myocardial infarction", "Healed myocardial infarct", "Old Myocardial Infarction", "PAST MYOCARDIAL INFARCTION", "prior myocardial infarction", "Infarction;myocardial;healed", "Healed myocardial infarction", "healed myocardial infarction", "previous myocardial infarction", "Previous myocardial infarction", "Myocardial infarction old healed", "infarction; myocardial, healed (old)", "Old myocardial infarction (disorder)", "infarction; myocardial, old (healed)", "previous myocardial infarction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Old myocardial infarction", "shortest_name_length": 11}
{"curie": "MONDO:0010555", "names": ["BCDP", "Cpxr", "CPXR", "CDXP1", "CDPX1", "Cdpx1", "Arylsulfatase E Deficiency", "arylsulfatase E deficiency", "X-Linked Chondrodysplasia Punctata 1", "X-linked chondrodysplasia punctata 1", "Chondrodysplasia Punctata 1, X-Linked", "arse X-linked chondrodysplasia punctata", "ARSE X-linked chondrodysplasia punctata", "Brachytelephalangic chondrodysplasia punctata", "brachytelephalangic chondrodysplasia punctata", "chondrodysplasia punctata brachytelephalangic", "Brachytelephalangic Chondrodysplasia Punctata", "BRACHYTELEPHALANGIC CHONDRODYSPLASIA PUNCTATA", "Chondrodysplasia punctata, brachytelephalangic", "chondrodysplasia punctata, brachytelephalangic", "chondrodysplasia punctata 1 X-linked recessive", "chondrodysplasia punctata, Brachytelephalangic", "X-Linked Recessive Chondrodysplasia Punctata 1", "CHONDRODYSPLASIA PUNCTATA, BRACHYTELEPHALANGIC", "CHONDRODYSPLASIA PUNCTATA 1, X-LINKED RECESSIVE", "chondrodysplasia punctata 1, X-linked recessive", "Chondrodysplasia punctata 1, X-linked recessive", "BCDP - brachytelephalangic chondrodysplasia punctata", "Brachytelephalangic chondrodysplasia punctata (disorder)", "CHONDRODYSPLASIA PUNCTATA, BRACHYTELEPHALANGIC, AUTOSOMAL", "X-linked chondrodysplasia punctata caused by mutation in arse", "X-linked chondrodysplasia punctata caused by mutation in ARSE", "chondrodysplasia punctata, X-linked recessive, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked chondrodysplasia punctata 1", "shortest_name_length": 4}
{"curie": "UMLS:C3203495", "names": ["Dyskinesia hyperpyrexia syndrome", "Parkinsonism hyperpyrexia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dyskinesia hyperpyrexia syndrome", "shortest_name_length": 32}
{"curie": "UMLS:C0521561", "names": ["corneal dystrophy macular congenital", "Congenital Macular Corneal Dystrophy", "congenital macular corneal dystrophy", "Congenital macular corneal dystrophy", "Congenital macular corneal dystrophy (disorder)", "congenital macular corneal dystrophy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital macular corneal dystrophy", "shortest_name_length": 36}
{"curie": "MONDO:0013085", "names": ["NBLST5", "neuroblastoma, susceptibility to, 5", "NEUROBLASTOMA, SUSCEPTIBILITY TO, 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuroblastoma, susceptibility to, 5", "shortest_name_length": 6}
{"curie": "UMLS:C2985226", "names": ["Substance-Induced Persisting Amnestic Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Substance-Induced Persisting Amnestic Disorder", "shortest_name_length": 46}
{"curie": "UMLS:C4528556", "names": ["Stage IIB Breast Cancer", "Anatomic Stage IIB Breast Cancer AJCC v8", "Anatomic Stage IIB Breast Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anatomic Stage IIB Breast Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "UMLS:C3146248", "names": ["Stage III Renal Cell Cancer", "Stage III Renal Cell Carcinoma", "Stage III Renal Cell Cancer AJCC v7", "Stage III Renal Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Renal Cell Cancer AJCC v7", "shortest_name_length": 27}
{"curie": "MONDO:0043280", "names": ["Wallerian degeneration", "wallerian degeneration", "Wallerian Degeneration", "Secondary degeneration", "degeneration secondary", "secondary degeneration", "Degeneration, secondary", "Degeneration, Wallerian", "Degeneration, secondary Wallerian", "Wallerian degeneration of the pyramidal tract", "Wallerian degeneration (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wallerian degeneration", "shortest_name_length": 22}
{"curie": "UMLS:C1112369", "names": ["Paranasal sinus hypersecretion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paranasal sinus hypersecretion", "shortest_name_length": 30}
{"curie": "UMLS:C3715147", "names": ["Necrotising myositis", "Necrotizing myositis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Necrotising myositis", "shortest_name_length": 20}
{"curie": "MONDO:0004135", "names": ["silent thyroiditis", "Silent thyroiditis", "Silent Thyroiditis", "Painless thyroiditis", "Subacute Painless Thyroiditis", "Silent thyroiditis (disorder)", "Subacute painless thyroiditis", "Subacute Lymphocytic Thyroiditis", "subacute lymphocytic thyroiditis", "Subacute lymphocytic thyroiditis", "Subacute lymphocytic thyroiditis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subacute lymphocytic thyroiditis", "shortest_name_length": 18}
{"curie": "MONDO:0022908", "names": ["cutis gyratum acanthosis nigricans craniosynostosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutis gyratum acanthosis nigricans craniosynostosis", "shortest_name_length": 51}
{"curie": "UMLS:C3501912", "names": ["Cerebrocostomandibular-Like Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebrocostomandibular-Like Syndrome", "shortest_name_length": 36}
{"curie": "MONDO:0003634", "names": ["Proteinuria", "PROTEINURIA", "proteinuria", "proteinurias", "Proteinurias", "Proteinuria, NOS", "Protein in urine", "Proteinuria (finding)", "Protein urine positive", "Positive urine protein", "proteinuria (diagnosis)", "Urinary protein positive", "Proteinuria, unspecified", "High urine protein levels", "Protein, urine, abnormal presence", "Abnormal presence of protein in urine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "proteinuria", "shortest_name_length": 11}
{"curie": "MONDO:0009282", "names": ["EMA", "ema", "GA2", "GA2B", "GA2C", "MADD", "Ga 2", "ACAD", "GA2A", "GA II", "MAD deficiency", "ETFB Deficiency", "ETFA DEFICIENCY", "Etfa deficiency", "ETFB DEFICIENCY", "Etfb deficiency", "ETFA Deficiency", "ETFDH Deficiency", "ETFDH DEFICIENCY", "Etfdh deficiency", "ETFA Deficiencies", "ETFB Deficiencies", "ETFDH Deficiencies", "glutaric acidemia 2", "glutaric aciduria 2", "glutaric acidemia 2B", "GLUTARIC ACIDEMIA II", "Glutaric Aciduria II", "GLUTARIC ACIDURIA II", "glutaric acidemia 2A", "glutaric acidemia 2C", "glutaric acidemia IIC", "Glutaric Aciduria IIA", "glutaric acidemia IIA", "GLUTARIC ACIDEMIA IIC", "Glutaric Aciduria IIC", "glutaric acidemia IIB", "Glutaric Aciduria IIB", "GLUTARIC ACIDEMIA IIA", "GLUTARIC ACIDEMIA IIB", "glutaric acidemia type 2", "Glutaric acidemia type 2", "Glutaric Aciduria Type 2", "glutaric aciduria type 2", "Glutaric Acidemia Type 2", "Glutaric aciduria type 2", "Glutaric Acidemia, Type 2", "Glutaric aciduria, type 2", "Glutaric Aciduria Type II", "Glutaric acidemia, type 2", "glutaric aciduria, type 2", "Glutaric aciduria type II", "Glutaric acidemia type II", "Glutaric Acidemia Type II", "glutaric acidemia type II", "glutaric aciduria type II", "Glutaric Aciduria, Type 2", "Glutaric acidaemia, type 2", "ethylmalonic-Adipicaciduria", "Ethylmalonic-adipicaciduria", "Ethylmalonic Adipicaciduria", "Ethylmalonic-Adipicaciduria", "ETHYLMALONIC-ADIPICACIDURIA", "Ethylmalonic-Adipic Aciduria", "Ethylmalonic Adipic Aciduria", "Ethylmalonic-Adipic Acidurias", "Aciduria, Ethylmalonic-Adipic", "Acidurias, Ethylmalonic-Adipic", "Glutaric aciduria, type 2 (disorder)", "glutaric aciduria type II (diagnosis)", "Multiple FAD Dehydrogenase Deficiency", "electron transfer flavoprotein deficiency", "Electron Transfer Flavoprotein Deficiency", "Multiple acyl-CoA dehydrogenase deficiency", "Multiple Acyl CoA Dehydrogenase Deficiency", "Multiple Acyl-CoA Dehydrogenase Deficiency", "multiple acyl-CoA dehydrogenase deficiency", "MULTIPLE ACYL-CoA DEHYDROGENASE DEFICIENCY", "Multiple acyl-CoA dehydrogenase deficiencies", "MAD - Multiple acyl-CoA dehydrogenase deficiency", "MADD - multiple acyl-CoA dehydrogenase deficiency", "MADD (Multiple Acyl-CoA Dehydrogenase Deficiency)", "MADD (Multiple Acyl CoA Dehydrogenase Deficiency)", "Multiple Acyl Coenzyme A Dehydrogenase Deficiency", "multiple acyl Coenzyme A dehydrogenase deficiency", "MADDs (Multiple Acyl-CoA Dehydrogenase Deficiency)", "Electron Transfer Flavoprotein Beta Subunit Deficiency", "Electron Transfer Flavoprotein Dehydrogenase Deficiency", "Electron Transfer Flavoprotein Alpha Subunit Deficiency", "electron transfer flavoprotein ubiquinone oxidoreductase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple acyl-CoA dehydrogenase deficiency", "shortest_name_length": 3}
{"curie": "UMLS:C1334934", "names": ["Neoplasm by Cause", "Neoplasm by Etiology"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplasm by Cause", "shortest_name_length": 17}
{"curie": "UMLS:C4283859", "names": ["CMM2", "Cutaneous Malignant Melanoma 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous Malignant Melanoma 2", "shortest_name_length": 4}
{"curie": "MONDO:0003843", "names": ["Cerebral Hemisphere Lipoma", "cerebral hemisphere lipoma", "lipoma of cerebral hemisphere", "Lipoma of Cerebral Hemisphere", "Lipoma of the Cerebral Hemisphere", "lipoma of the cerebral hemisphere"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral hemisphere lipoma", "shortest_name_length": 26}
{"curie": "MONDO:0017927", "names": ["severe lateral tibial bowing with short stature", "Severe lateral tibial bowing with short stature", "Severe lateral tibial bowing with short stature (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe lateral tibial bowing with short stature", "shortest_name_length": 47}
{"curie": "UMLS:C5418887", "names": ["Metastatic Ovarian Carcinosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Ovarian Carcinosarcoma", "shortest_name_length": 33}
{"curie": "MONDO:0015929", "names": ["thoracic malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thoracic malformation", "shortest_name_length": 21}
{"curie": "UMLS:C0333371", "names": ["drain abscess", "Abscess rupture", "ABSCESS DRAINING", "Ruptured abscess", "ruptured abscess", "rupture; abscess", "Draining abscess", "abscess draining", "Abscess, draining", "abscesses draining", "Abscess, ruptured and draining", "Ruptured abscess (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ruptured abscess", "shortest_name_length": 13}
{"curie": "UMLS:C5670732", "names": ["Anorectal Dysfunction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anorectal Dysfunction", "shortest_name_length": 21}
{"curie": "UMLS:C4763673", "names": ["High Risk NMIBC", "High Risk Non-Muscle Invasive Bladder Urothelial Carcinoma", "High Risk, Non-Muscle Invasive Bladder Urothelial Carcinoma", "High-Risk, Non-Muscle Invasive Bladder Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Risk Non-Muscle Invasive Bladder Urothelial Carcinoma", "shortest_name_length": 15}
{"curie": "UMLS:C0520723", "names": ["periorbital hematoma", "Periorbital hematoma", "hematoma periorbital", "Periorbital haematoma", "peri-orbital hematoma", "peri-orbital haematoma", "Haematoma;peri-orbital", "haematomas periorbital", "Periorbital hematoma (disorder)", "periorbital hematoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Periorbital hematoma", "shortest_name_length": 20}
{"curie": "UMLS:C0341011", "names": ["lip venous lake", "venous lake lip", "Venous lake of lip", "Venous varix of lip", "Cherry Hemangioma of Lip", "Senile hemangioma of lip", "senile hemangioma of lip", "Senile Hemangioma of Lip", "Senile haemangioma of lip", "Senile hemangioma of lip (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Senile hemangioma of lip", "shortest_name_length": 15}
{"curie": "UMLS:C1142025", "names": ["Stage IV Esophageal Squamous Cell Carcinoma", "Esophageal squamous cell carcinoma stage IV", "Oesophageal squamous cell carcinoma stage IV", "Esophageal squamous cell carcinoma metastatic", "Metastatic Esophageal Squamous Cell Carcinoma", "Oesophageal squamous cell carcinoma metastatic", "Esophageal squamous cell carcinoma site unspecified stage IV", "Oesophageal squamous cell carcinoma site unspecified stage IV"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Esophageal Squamous Cell Carcinoma", "shortest_name_length": 43}
{"curie": "UMLS:C5420340", "names": ["Recurrent Pharyngeal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Pharyngeal Squamous Cell Carcinoma", "shortest_name_length": 44}
{"curie": "MONDO:0013422", "names": ["C8D1", "C81 deficiency", "C8AG DEFICIENCY", "C8Ag deficiency", "C8 deficiency type I", "C8 deficiency, type I", "C8 deficiency, type 1", "C8 DEFICIENCY, TYPE I", "C8 Alpha-gamma deficiency", "C8 ALPHA-GAMMA DEFICIENCY", "type I complement component 8 deficiency", "complement component 8 deficiency type I", "complement component 8 deficiency type 1", "complement component 8 deficiency, type 1", "COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE I", "complement component 8 deficiency, type I", "C8A classic complement early component deficiency", "classic complement early component deficiency caused by mutation in C8A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type I complement component 8 deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0018087", "names": ["VHF", "VHFs", "HEMORRHAGIC FEVER", "hemorrhagic fever", "fever hemorrhagic", "Hemorrhagic fever", "Hemorrhagic Fever", "Hemorrhagic Fevers", "hemorrhagic fevers", "haemorrhagic fever", "fevers hemorrhagic", "Haemorrhagic fever", "fever; hemorrhagic", "Hemorrhagic fever NOS", "Haemorrhagic fever NOS", "Viral Hemorrhagic Fever", "viral hemorrhagic fever", "fever hemorrhagic viral", "Viral hemorrhagic fever", "hemorrhagic fever; viral", "Viral Hemorrhagic Fevers", "viral; hemorrhagic fever", "Fever, Viral Hemorrhagic", "viral hemorrhagic fevers", "Viral haemorrhagic fever", "Hemorrhagic Fever, Viral", "viral haemorrhagic fever", "virus; hemorrhagic fever", "fevers haemorrhagic viral", "Hemorrhagic Fevers, Viral", "Fevers, Viral Hemorrhagic", "fever; hemorrhagic, viral", "haemorrhagic fevers, viral", "VHF - Viral hemorrhagic fever", "VHF - Viral haemorrhagic fever", "Viral hemorrhagic fever (disorder)", "infection; viral, hemorrhagic fever", "viral hemorrhagic fever (diagnosis)", "Unspecified viral hemorrhagic fever", "Unspecified viral haemorrhagic fever"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "viral hemorrhagic fever", "shortest_name_length": 3}
{"curie": "UMLS:C1737219", "names": ["Acute graft versus host disease in intestine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute graft versus host disease in intestine", "shortest_name_length": 44}
{"curie": "MONDO:0013918", "names": ["tetrasomy 15q26", "TETRASOMY 15q26", "Tetrasomy 15q26", "Distal tetrasomy 15q", "tetrasomy type 15Q26", "distal tetrasomy 15q", "levy-Shanske syndrome", "LEVY-SHANSKE SYNDROME", "Tetrasomy 15(q25-qter)", "tetrasomy 15(q25-qter)", "distal tetrasomy type 15q"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal tetrasomy 15q", "shortest_name_length": 15}
{"curie": "MONDO:0012603", "names": ["EKD2", "DYT19", "Dystonia 19", "dystonia 19", "DYSTONIA 19", "Episodic Kinesigenic Dyskinesia 2", "episodic kinesigenic dyskinesia 2", "EPISODIC KINESIGENIC DYSKINESIA 2", "episodic kinesigenic dyskinesia type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "episodic kinesigenic dyskinesia 2", "shortest_name_length": 4}
{"curie": "MONDO:0016214", "names": ["pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome", "shortest_name_length": 70}
{"curie": "UMLS:C0858775", "names": ["Myopia transient"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myopia transient", "shortest_name_length": 16}
{"curie": "MONDO:0022805", "names": ["colonic malakoplakia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colonic malakoplakia", "shortest_name_length": 20}
{"curie": "MONDO:0005480", "names": ["contact eczema", "Contact eczema", "Contact Eczema", "contact; eczema", "eczema; contact", "Bandage allergy", "Eczema, Contact", "CONTACT DEMATITIS", "DERMATITIS CONTACT", "Dermatitis contact", "contact dermatitis", "Dermatitis;contact", "Contact Dermatitis", "Contact dermatitis", "CONTACT DERMATITIS", "DERMATITIS VENENATA", "contact; dermatitis", "DERMATITIS, CONTACT", "Contact Sensitivity", "Dermatitis venenata", "dermatitis venenata", "dermatitis; contact", "Dermatitis Venenata", "contact sensitivity", "Dermatitis, Contact", "dermatitis, venenata", "Sensitivity, Contact", "Dermatitis, venenata", "Contact Dermatitides", "Contact Sensitivities", "Dermatitides, Contact", "Sensitivities, Contact", "Contact dermatitis, NOS", "Dermatitis, contact NOS", "CD - Contact dermatitis", "Dermatitis, venenata NOS", "Contact dermatitis/eczema", "contact dermatitis/eczema", "Contact dermatitis syndrome", "Contact dermatitis (disorder)", "contact dermatitis (diagnosis)", "Unspecified contact dermatitis", "dermatitis venenata (diagnosis)", "Unspecified contact dermatitis, unspecified cause"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "contact dermatitis", "shortest_name_length": 14}
{"curie": "MONDO:0001153", "names": ["transsexualism", "dysphoria gender", "Gender Dysphoria", "Gender dysphoria", "gender dysphoria", "Gender incongruence", "Gender dysphoria, NOS", "Gender Identity Disorder", "Gender Identity Disorders", "Identity Disorder, Gender", "Disorder, Gender Identity", "Gender identity dysphoria", "Gender dysphoria (disorder)", "gender dysphoria (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gender dysphoria", "shortest_name_length": 14}
{"curie": "MONDO:0010784", "names": ["CHLORAMPHENICOL TOXICITY", "chloramphenicol toxicity", "chloramphenicol resistance", "toxicity from chloramphenicol", "ANEMIA, CHLORAMPHENICOL-INDUCED", "anemia, chloramphenicol-induced", "chloramphenicol toxicity (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chloramphenicol toxicity", "shortest_name_length": 24}
{"curie": "UMLS:C2212425", "names": ["Renal Small Cell Carcinoma", "Kidney Small Cell Carcinoma", "small cell carcinoma of kidney", "small cell carcinoma of kidney (diagnosis)", "Kidney Small Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small cell carcinoma of kidney", "shortest_name_length": 26}
{"curie": "MONDO:0100103", "names": ["FADS3", "fetal akinesia deformation sequence 3", "FETAL AKINESIA DEFORMATION SEQUENCE 3", "fetal akinesia deformation sequence syndrome 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fetal akinesia deformation sequence 3", "shortest_name_length": 5}
{"curie": "MONDO:0013055", "names": ["Stargardt macular degeneration absent or hypoplastic corpus callosum mental retardation and dysmorphic features", "Stargardt Macular Degeneration Absent or Hypoplastic Corpus Callosum Mental Retardation and Dysmorphic Features", "Stargardt macular degeneration, absent or hypoplastic corpus callosum, mental retardation, and dysmorphic features", "Stargardt macular degeneration absent or hypoplastic corpus callosum intellectual disability and dysmorphic features", "Stargardt macular degeneration, absent or hypoplastic corpus callosum, intellectual disability, and dysmorphic features", "STARGARDT MACULAR DEGENERATION, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, MENTAL RETARDATION, AND DYSMORPHIC FACIAL FEATURES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stargardt macular degeneration, absent or hypoplastic corpus callosum, intellectual disability, and dysmorphic features", "shortest_name_length": 111}
{"curie": "UMLS:C1519927", "names": ["Vaginal Non-Keratinizing Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Non-Keratinizing Squamous Cell Carcinoma", "shortest_name_length": 48}
{"curie": "MONDO:0012879", "names": ["SCZD14", "Sczd14", "SCHIZOPHRENIA 14", "schizophrenia 14", "schizophrenia type 14", "schizophrenia, susceptibility to, 14", "schizophrenia susceptibility locus, chromosome 2Q32-related", "SCHIZOPHRENIA SUSCEPTIBILITY LOCUS, CHROMOSOME 2q32-RELATED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schizophrenia 14", "shortest_name_length": 6}
{"curie": "UMLS:C0265099", "names": ["a.basilaris; thrombosis", "Basilar artery thrombosis", "basilar artery thrombosis", "thrombosis; basilar artery", "Basilar artery thrombosis (disorder)", "basilar artery thrombosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Basilar artery thrombosis", "shortest_name_length": 23}
{"curie": "UMLS:C0149836", "names": ["Senile vulvovaginitis", "Vulvovaginitis atrophy", "Vulvovaginitis atrophic", "Atrophic vulvovaginitis", "ATROPHIC VULVOVAGINITIS", "vulvovaginitis atrophic", "Atrophic vulvovaginitis (disorder)", "Atrophic vulvovaginitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atrophic vulvovaginitis", "shortest_name_length": 21}
{"curie": "MONDO:0012882", "names": ["MAFD9", "major affective disorder 9", "BIPOLAR AFFECTIVE DISORDER", "MAJOR affective disorder 9", "MAJOR AFFECTIVE DISORDER 9", "bipolar affective disorder", "Major Affective Disorder 9", "major affective disorder-9, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "major affective disorder 9", "shortest_name_length": 5}
{"curie": "UMLS:C4525395", "names": ["Distal Bile Duct Cancer by AJCC v7 Stage", "Distal Bile Duct Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Distal Bile Duct Cancer by AJCC v7 Stage", "shortest_name_length": 40}
{"curie": "MONDO:0011977", "names": ["NMLFS", "Monosomy 8q22.1", "monosomy 8q22.1", "8q22.1 microdeletion syndrome", "NABLUS MASK-LIKE FACIAL SYNDROME", "Nablus mask-like facial syndrome", "NABLUS mask-like facial syndrome", "chromosome 8Q22.1 deletion syndrome", "CHROMOSOME 8q22.1 DELETION SYNDROME", "8q22.1 microdeletion syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "8q22.1 microdeletion syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0005402", "names": ["Lymphoid Leukemia", "leukemia lymphoid", "Lymphoid leukemia", "Leukemia lymphoid", "LEUKEMIA LYMPHOID", "lymphoid leukemia", "Lymphoid Leukemias", "LYMPHOID LEUKEMIAS", "Lymphoid leukemias", "LEUKEMIA LYMPHATIC", "lymphatic leukemia", "Leukaemia lymphoid", "LEUKAEMIA LYMPHOID", "Leukemia lymphatic", "Lymphoid leukaemia", "lymphoid leukaemia", "Lymphatic leukemia", "Leukemia, Lymphoid", "Lymphoid leukaemias", "leukemia; lymphatic", "Leukemias, Lymphoid", "lymphatic; leukemia", "lymphatic leukaemia", "Lymphatic leukaemia", "Leukaemia lymphatic", "LEUKAEMIA LYMPHATIC", "leukemia lymphocytic", "Leukemia lymphocytic", "Lymphocytic leukemia", "LYMPHOCYTIC LEUKEMIA", "Lymphocytic Leukemia", "LEUKEMIA LYMPHOCYTIC", "lymphocytic leukemia", "lymphocytic leukaemia", "lymphogenous leukemia", "[M]Lymphoid leukemias", "Lymphocytic Leukemias", "Lymphoid leukemia NOS", "Leukaemia lymphocytic", "Leukemia, Lymphocytic", "LEUKAEMIA LYMPHOCYTIC", "Lymphocytic leukaemia", "Lymphogenous Leukemia", "Lymphoid leukaemia NOS", "leukemia lymphoblastic", "Lymphoblastic leukemia", "lymphoblastic leukemia", "Lymphoid leukemia, NOS", "[M]Lymphoid leukaemias", "Leukemias, Lymphocytic", "lymphoblastic; leukemia", "Lymphoid leukaemia, NOS", "Lymphatic leukemia, NOS", "leukemia; lymphoblastic", "Lymphatic leukaemia, NOS", "Lymphocytic leukemia, NOS", "Lymphocytic leukaemia, NOS", "Subacute lymphoid leukemia", "Lymphoblastic leukemia NOS", "subacute lymphoid leukemia", "Lymphoid leukemia, subacute", "lymphoid leukemia (disease)", "Lymphoblastic leukaemia NOS", "Subacute lymphoid leukaemia", "Subacute lymphatic leukemia", "Subacute lymphatic leukaemia", "Lymphoid leukaemia, subacute", "Lymphoid leukemia (disorder)", "leukemia; lymphatic, subacute", "subacute lymphocytic leukemia", "Unspecified lymphoid leukemia", "[M]Subacute lymphoid leukemia", "Subacute lymphocytic leukemia", "lymphatic; leukemia, subacute", "leukemia lymphocytic subacute", "[M]Subacute lymphoid leukaemia", "Subacute lymphocytic leukaemia", "Lymphoid leukemia, unspecified", "Unspecified lymphoid leukaemia", "Lymphoid leukaemia, unspecified", "LEUKEMIA, LYMPHOCYTIC, MALIGNANT", "leukemia, LYMPHOCYTIC, malignant", "lymphocytic leukemia (diagnosis)", "Subacute lymphoid leukemia (disorder)", "subacute lymphocytic leukemia (diagnosis)", "Lymphoid leukemia (morphologic abnormality)", "Subacute lymphoid leukemia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphoid leukemia", "shortest_name_length": 17}
{"curie": "UMLS:C3853041", "names": ["Severe Congenital Microcephaly", "Microcephaly, Severe Congenital", "Congenital Microcephaly, Severe", "Severe Congenital Microcephalies", "Microcephalies, Severe Congenital", "Congenital Microcephalies, Severe"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Severe Congenital Microcephaly", "shortest_name_length": 30}
{"curie": "MONDO:0019448", "names": ["FAME", "ADCME", "BAFME", "FCMTE", "familial adult myoclonic epilepsy", "Familial adult myoclonic epilepsy", "benign adult familial myoclonus epilepsy", "benign adult familial myoclonic epilepsy", "Benign adult familial myoclonic epilepsy", "Benign adult familial myoclonus epilepsy", "Familial cortical myoclonic tremor and epilepsy", "familial cortical myoclonic tremor and epilepsy", "BAFME - Benign adult familial myoclonic epilepsy", "Autosomal dominant cortical myoclonus and epilepsy", "autosomal dominant cortical myoclonus and epilepsy", "Benign adult familial myoclonic epilepsy (disorder)", "Benign adult familial myoclonic epilepsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign adult familial myoclonic epilepsy", "shortest_name_length": 4}
{"curie": "MONDO:0012954", "names": ["CRCS11", "colorectal cancer, susceptibility to, 11", "COLORECTAL CANCER, SUSCEPTIBILITY TO, 11", "COLORECTAL CANCER, SUSCEPTIBILITY TO, ON CHROMOSOME 20p", "colorectal cancer, susceptibility to, on chromosome 20P"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorectal cancer, susceptibility to, 11", "shortest_name_length": 6}
{"curie": "UMLS:C0752199", "names": ["Adult-Onset Idiopathic Torsion Dystonias", "Adult Onset Idiopathic Torsion Dystonias"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult-Onset Idiopathic Torsion Dystonias", "shortest_name_length": 40}
{"curie": "UMLS:C4721650", "names": ["Stage III Esophageal Squamous Cell Cancer", "Stage III Esophagus Squamous Cell Carcinoma", "Esophageal Squamous Cell Carcinoma Stage III", "Stage III Esophageal Squamous Cell Carcinoma", "Oesophageal Squamous Cell Carcinoma Stage III", "Stage III Squamous Cell Carcinoma of Esophagus", "Stage III Squamous Cell Carcinoma of the Esophagus", "Stage III Esophageal Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Esophageal Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 41}
{"curie": "MONDO:0013087", "names": ["BESC2", "bronchiectasis 2", "SCNN1A bronchiectasis", "cystic fibrosis-like syndrome", "CYSTIC FIBROSIS-LIKE SYNDROME", "bronchiectasis caused by mutation in SCNN1A", "BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 2", "Bronchiectasis With Or Without Elevated Sweat Chloride 2", "bronchiectasis with or without elevated sweat chloride 2", "bronchiectasis with or without elevated sweat chloride type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bronchiectasis with or without elevated sweat chloride 2", "shortest_name_length": 5}
{"curie": "MONDO:0016373", "names": ["isolated facial myokymia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated facial myokymia", "shortest_name_length": 24}
{"curie": "MONDO:0001207", "names": ["Respiratory failure neonatal", "Neonatal respiratory failure", "neonatal respiratory failure", "Respiratory failure, neonatal", "respiratory failure of newborn", "Respiratory failure of newborn", "Neonatal respiratory failure, NOS", "Neonatal respiratory failure (disorder)", "respiratory failure of newborn (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal respiratory failure", "shortest_name_length": 28}
{"curie": "MONDO:0021107", "names": ["NARCOLEPSY", "narcolepsy", "Narcolepsy", "narcolepsies", "Narcolepsy NOS", "paroxysmal sleep", "PAROXYSMAL SLEEP", "Paroxysmal Sleep", "Paroxysmal sleep", "GELINEAU SYNDROME", "Gelineau Syndrome", "gelineau syndrome", "Sleep, Paroxysmal", "SLEEP, PAROXYSMAL", "Gelineaus Syndrome", "Syndrome, Gelineau", "Gelineau's Syndrome", "gélineau's syndrome", "narcolepsy disorder", "Gelineau's syndrome", "gelineau's syndrome", "narcoleptic syndrome", "Narcoleptic syndrome", "Syndrome, Gelineau's", "Narcoleptic Syndrome", "Gelineau's Syndromes", "Narcolepsy (disorder)", "Narcoleptic Syndromes", "Syndrome, Narcoleptic", "Syndromes, Gelineau's", "Syndromes, Narcoleptic", "narcolepsy (diagnosis)", "Narcolepsy, without cataplexy", "narcolepsy, without cataplexy", "obsolete_narcolepsy with cataplexy", "Narcolepsy with or without cataplexy", "excessive uncontrollable daytime sleepiness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "narcolepsy", "shortest_name_length": 10}
{"curie": "UMLS:C5237057", "names": ["Refractory Endometrial Dedifferentiated Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Endometrial Dedifferentiated Carcinoma", "shortest_name_length": 49}
{"curie": "MONDO:0009183", "names": ["JEB5B", "Eb-Pa", "Pa-Jeb", "JEB-Pa", "PA-JEB", "JEB-PA", "EB-PA-ACC", "EB-Pa-ACC", "Carmi syndrome", "CARMI SYNDROME", "Carmi Syndrome", "JEB with pyloric atresia", "Epidermolysis bullosa with pyloric atresia", "epidermolysis bullosa with pyloric atresia", "junctional epidermolysis bullosa - pyloric atresia", "APLASIA CUTIS CONGENITA WITH GASTROINTESTINAL ATRESIA", "Junctional epidermolysis bullosa with pyloric atresia", "Aplasia cutis congenita with gastrointestinal atresia", "junctional epidermolysis bullosa with pyloric atresia", "JUNCTIONAL EPIDERMOLYSIS BULLOSA WITH PYLORIC ATRESIA", "Junctional Epidermolysis Bullosa With Pyloric Atresia", "aplasia cutis congenita with gastrointestinal atresia", "Epidermolysis Bullosa, Junctional, with Pyloric Atresia", "epidermolysis bullosa, junctional, with pyloric atresia", "Epidermolysis Bullosa, Junctional, With Pyloric Atresia", "epidermolysis bullosa junctionalis with pyloric atresia", "EPIDERMOLYSIS BULLOSA JUNCTIONALIS WITH PYLORIC ATRESIA", "EPIDERMOLYSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA", "Epidermolysis Bullosa Junctionalis With Pyloric Atresia", "epidermolysis bullosa JUNCTIONALIS with pyloric atresia", "epidermolysis bullosa, junctional, with pyloric stenosis", "junctional epidermolysis bullosa-pyloric atresia syndrome", "EPIDERMOLYSIS BULLOSA, JUNCTIONAL 5B, WITH PYLORIC ATRESIA", "epidermolysis bullosa, junctional, with pyloric atresia and aplasia cutis congenita", "Epidermylosis Bullosa, Junctional, With Pyloric Atresia And Aplasia Cutis Congenita", "EPIDERMOLYSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA AND APLASIA CUTIS CONGENITA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "junctional epidermolysis bullosa with pyloric atresia", "shortest_name_length": 5}
{"curie": "MONDO:0012725", "names": ["LPG", "LIPOPROTEIN GLOMERULOPATHY", "lipoprotein glomerulopathy", "glomerulopathy lipoprotein", "Lipoprotein glomerulopathy", "Lipoprotein Glomerulopathy", "Lipoprotein glomerulopathy (disorder)", "Lipoprotein glomerulopathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lipoprotein glomerulopathy", "shortest_name_length": 3}
{"curie": "MONDO:0009544", "names": ["MGCPH", "Fryns Dereymaeker Haegeman syndrome", "MACROCEPHALY/MEGALENCEPHALY SYNDROME, AUTOSOMAL RECESSIVE", "macrocephaly/megalencephaly syndrome, autosomal recessive", "Mental retardation, macrocephaly, short stature and craniofacial dysmorphism", "mental retardation, macrocephaly, short stature and craniofacial dysmorphism", "intellectual disability, macrocephaly, short stature and craniofacial dysmorphism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macrocephaly/megalencephaly syndrome, autosomal recessive", "shortest_name_length": 5}
{"curie": "UMLS:C2985225", "names": ["Substance Withdrawal Delirium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Substance Withdrawal Delirium", "shortest_name_length": 29}
{"curie": "MONDO:0017607", "names": ["SDAM", "sacral agenesis", "caudal dysplasia", "CAUDAL DYSPLASIA", "Caudal Dysplasia", "sacral agenesis syndrome", "SACRAL AGENESIS SYNDROME", "Sacral Agenesis Syndrome", "caudal dysplasia sequence", "caudal regression syndrome", "caudal dysgenesis syndrome", "caudal regression sequence", "sacral regression syndrome", "Sacral defect anterior meningocele", "Sacral Defect with Anterior Meningocele", "SACRAL DEFECT WITH ANTERIOR MENINGOCELE", "sacral defect with anterior meningocele", "Sacral defect and anterior sacral meningocele"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "caudal regression sequence", "shortest_name_length": 4}
{"curie": "MONDO:0020726", "names": ["MCKD", "Mckd", "MCKD1", "ADTKD2", "ADMCKD1", "ADTKD-MUC1", "MUCI-related ADTKD", "Medullary cystic kidney disease 1", "medullary cystic kidney disease 1", "MEDULLARY CYSTIC KIDNEY DISEASE 1", "polycystic kidneys, medullary type", "POLYCYSTIC KIDNEYS, MEDULLARY TYPE", "Polycystic kidneys, medullary type", "Medullary Cystic Kidney Disease Type I", "Medullary cystic kidney disease type 1", "medullary cystic kidney disease type 1", "medullary cystic kidney disease - MCKD1", "MCKD1 Medullary cystic kidney disease 1", "MUC1-related medullary cystic kidney disease", "Autosomal Dominant Interstitial Kidney Disease", "MEDULLARY CYSTIC KIDNEY DISEASE, AUTOSOMAL DOMINANT", "Medullary cystic kidney disease, autosomal dominant", "medullary cystic kidney disease, autosomal dominant", "medullary cystic kidney disease - MCKD1 (diagnosis)", "tubulointerstitial kidney disease, autosomal dominant, 2", "TUBULOINTERSTITIAL KIDNEY DISEASE, AUTOSOMAL DOMINANT, 2", "MUC1-related autosomal dominant medullary cystic kidney disease", "MUC1-related autosomal dominant tubulointerstitial kidney disease", "Mucin 1 related autosomal dominant tubulointerstitial kidney disease", "autosomal dominant medullary cystic kidney disease without hyperuricemia", "Autosomal dominant medullary cystic kidney disease without hyperuricemia", "Autosomal dominant medullary cystic kidney disease without hyperuricaemia", "autosomal dominant tubulointerstitial kidney disease due to mutations in MUC1", "Mucin 1 related autosomal dominant tubulointerstitial kidney disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tubulointerstitial kidney disease, autosomal dominant, 2", "shortest_name_length": 4}
{"curie": "UMLS:C0156128", "names": ["Obstructed femoral hernia", "Femoral hernia, obstructive", "Femoral hernia with obstruction", "femoral hernia with obstruction", "Femoral Hernia with Obstruction", "hernia; femoral, with obstruction", "Obstructed femoral hernia (disorder)", "Femoral hernia, with obstruction NOS", "femoral hernia with obstruction (diagnosis)", "Femoral hernia specified as causing obstruction", "Obstruction co-occurrent and due to femoral hernia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Obstructed femoral hernia", "shortest_name_length": 25}
{"curie": "MONDO:0014091", "names": ["MC5DN4", "MC5DN4B", "ATP5F1A mitochondrial complex deficiency", "MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATP5A1 TYPE", "mitochondrial complex deficiency caused by mutation in ATP5F1A", "mitochondrial Complex 5 (ATP synthase) deficiency, ATP5A1 type", "mitochondrial complex V (ATP synthase) deficiency nuclear type 4", "mitochondrial complex V (ATP synthase) deficiency nuclear type 4B", "mitochondrial Complex 5 (ATP synthase) deficiency, nuclear type 4", "MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4", "mitochondrial complex V (ATP synthase) deficiency, nuclear type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex V (ATP synthase) deficiency nuclear type 4", "shortest_name_length": 6}
{"curie": "MONDO:0003065", "names": ["Nasal Cavity Inverted Papilloma", "nasal cavity inverted papilloma", "nasal cavity inverting papilloma", "Inverting Papilloma of Nasal Cavity", "inverting papilloma of nasal cavity", "Inverting papilloma of the nasal cavity", "inverting papilloma of the nasal cavity", "Inverting Papilloma of the Nasal Cavity", "Nasal Cavity Inverted Schneiderian Papilloma", "nasal cavity Schneiderian papilloma, inverted type", "Nasal Cavity Schneiderian Papilloma, Inverted Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasal cavity inverting papilloma", "shortest_name_length": 31}
{"curie": "UMLS:C5446666", "names": ["Locally Advanced Osteosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Osteosarcoma", "shortest_name_length": 29}
{"curie": "UMLS:C1335701", "names": ["Recurrent Follicular Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Follicular Lymphoma", "shortest_name_length": 29}
{"curie": "MONDO:0006970", "names": ["sialolith", "Sialolith", "Sialoliths", "sialoliths", "sialolithiasis", "SIALOLITHIASIS", "salivary stone", "Salivary stone", "Sialolithiasis", "salivary stones", "salivary calculus", "Salivary calculus", "gland salivary stone", "Salivary Gland Stone", "Salivary gland Stone", "salivary gland stone", "salivary gland Stone", "Stone, Salivary Gland", "Gland Stone, Salivary", "glands salivary stone", "gland salivary stones", "salivary gland stones", "Salivary Gland Stones", "Stones, Salivary Gland", "Gland Stones, Salivary", "glands salivary stones", "Salivary Gland Calculi", "Calculi, Salivary Gland", "Salivary Gland Calculus", "Stone of salivary gland", "Calculus salivary gland", "Salivary gland calculus", "Gland Calculi, Salivary", "Gland Calculus, Salivary", "salivary gland; calculus", "calculus; salivary gland", "Calculus, Salivary Gland", "Sialolithiasis (disorder)", "calculus of salivary gland", "Calculus of salivary gland", "salivary calculus (diagnosis)", "Stone of salivary gland or duct", "Calculus of salivary gland or duct", "salivary calculus (physical finding)", "calculus of salivary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sialolithiasis", "shortest_name_length": 9}
{"curie": "MONDO:0000784", "names": ["melon allergy", "Cucumis melo fruit allergy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melon allergy", "shortest_name_length": 13}
{"curie": "MONDO:0034106", "names": ["DEE73", "EIEE73", "RNF13-related severe EOEE", "early infantile epileptic encephalopathy 73", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 73", "developmental and epileptic encephalopathy 73", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 73", "epileptic encephalopathy, early infantile, 73", "developmental and epileptic encephalopathy, 73", "rnf13-related severe early-onset epileptic encephalopathy", "RNF13-related severe early-onset epileptic encephalopathy", "Ring finger protein 13-related severe early-onset epileptic encephalopathy", "Ring finger protein 13-related severe early-onset epileptic encephalopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 73", "shortest_name_length": 5}
{"curie": "UMLS:C5420541", "names": ["Locally Advanced Endometrial Endometrioid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Endometrial Endometrioid Adenocarcinoma", "shortest_name_length": 56}
{"curie": "UMLS:C4525138", "names": ["Stage III Rectal Cancer", "Stage III Rectal Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Rectal Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "MONDO:0012338", "names": ["EIG4", "idiopathic generalized epilepsy 4", "epilepsy, idiopathic generalized, susceptibility to 4", "EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 4", "epilepsy, idiopathic generalized, susceptibility to, 4", "EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 4 (finding)", "epilepsy, idiopathic generalized, susceptibility to, locus on chromosome 10", "EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, LOCUS ON CHROMOSOME 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, idiopathic generalized, susceptibility to, 4", "shortest_name_length": 4}
{"curie": "MONDO:0014821", "names": ["OCLSBG", "complex lethal osteochondrodysplasia", "Complex lethal osteochondrodysplasia", "Complex lethal osteochondrodysplasia (disorder)", "Complex lethal osteochondrodysplasia Symoens Barnes Gistelinck type", "Complex lethal osteochondrodysplasia, Symoens-Barnes-Gistelinck type", "osteochondrodysplasia, COMPLEX lethal, Symoens-Barnes-Gistelinck type", "osteochondrodysplasia, Complex lethal, Symoens-Barnes-Gistelinck type", "OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complex lethal osteochondrodysplasia", "shortest_name_length": 6}
{"curie": "UMLS:C0152451", "names": ["Glomerulonephritis;chronic", "chronic glomerulonephritis", "Glomerulonephritis chronic", "Chronic glomerulonephritis", "Chronic Glomerulonephritis", "GLOMERULONEPHRITIS, CHRONIC", "chronic; glomerulonephritis", "glomerulonephritis; chronic", "Nephritis specified as chronic", "Chronic glomerulonephritis, NOS", "CGN - Chronic glomerulonephritis", "Chronic glomerulonephritis syndrome", "Chronic glomerulonephritis (disorder)", "chronic glomerulonephritis (diagnosis)", "Glomerulonephritis NOS specified as chronic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic glomerulonephritis", "shortest_name_length": 26}
{"curie": "UMLS:C0746343", "names": ["Localized Lymphoma", "LYMPHOMA LOCALIZED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized Lymphoma", "shortest_name_length": 18}
{"curie": "UMLS:C2985220", "names": ["Anaplastic Medulloblastoma", "Anaplastic medulloblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anaplastic Medulloblastoma", "shortest_name_length": 26}
{"curie": "MONDO:0012864", "names": ["SAS", "glass", "GLASS", "Del(2)(q32)", "Monosomy 2q32", "monosomy 2q32", "glass syndrome", "SATB2 syndrome", "Del(2)(q32q33)", "Glass syndrome", "GLASS SYNDROME", "monosomy 2q32q33", "Monosomy 2q32q33", "monosomy 2q32-q33", "SATB2-associated syndrome", "2q32q33 microdeletion syndrome", "2q32-q33 microdeletion syndrome", "2q32q33 microdeletion syndromes", "CHROMOSOME 2q32-q33 DELETION SYNDROME", "Chromosome 2q32-Q33 Deletion Syndrome", "chromosome 2q32-q33 deletion syndrome", "2q32q33 microdeletion syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 2q32-q33 deletion syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C1336328", "names": ["Ureter Cancer Stage II", "Stage II Ureter Cancer", "Stage II Ureter Carcinoma", "Stage II Ureteral Carcinoma", "Stage II Carcinoma of Ureter", "Stage II Ureter Cancer AJCC v7", "Stage II Carcinoma of the Ureter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Ureter Cancer AJCC v7", "shortest_name_length": 22}
{"curie": "MONDO:0015233", "names": ["caudal appendage deafness", "Lynch-Lee-Murday syndrome", "Lynch Lee Murday syndrome", "caudal appendage-deafness syndrome", "Caudal appendage deafness syndrome", "caudal appendage deafness syndrome", "Caudal appendage-deafness syndrome", "Caudal appendage-hearing loss syndrome", "Caudal appendage deafness syndrome (disorder)", "caudal appendage deafness syndrome (diagnosis)", "Caudal appendage, short terminal phalanges, deafness, cryptorchidism and mental retardation", "caudal appendage, short terminal phalanges, deafness, cryptorchidism and mental retardation", "caudal appendage, short terminal phalanges, deafness, cryptorchidism and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "caudal appendage-deafness syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0016760", "names": ["Seemanova Lesny syndrome", "Seemanova-Lesny syndrome", "microcephaly microcornea syndrome Seemanova type", "Microcephaly microcornea syndrome Seemanova type", "microcephaly-microcornea syndrome, Seemanova type", "Microcephaly-microcornea syndrome, Seemanova type", "Microcephalus microcornea syndrome of Seemanova type", "[OBSOLETE] Microcephaly microcornea syndrome Seemanova type", "Microcephalus microcornea syndrome of Seemanova type (disorder)", "X-linked microcephaly-microphthalmia-microcornea-cataract-hypogenitalism-mental retardation-spasticity syndrome", "X-linked microcephaly, microphthalmia, microcornea, congenital cataract, hypogenitalism, mental deficiency, growth retardation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly-microcornea syndrome, Seemanova type", "shortest_name_length": 24}
{"curie": "MONDO:0054726", "names": ["SPGF22", "spermatogenic failure 22", "SPERMATOGENIC FAILURE 22"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 22", "shortest_name_length": 6}
{"curie": "UMLS:C4553251", "names": ["Stage IIA Fallopian Tube Cancer", "Stage IIA Fallopian Tube Cancer AJCC v8", "Stage IIA Fallopian Tube Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Fallopian Tube Cancer AJCC v8", "shortest_name_length": 31}
{"curie": "UMLS:C4683598", "names": ["Lugano Classification Stage II Childhood Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage II Childhood Hodgkin Lymphoma AJCC v8", "shortest_name_length": 65}
{"curie": "MONDO:0008090", "names": ["CH", "CN", "CyN", "Cyclic neutropenia", "CYCLIC NEUTROPENIA", "cyclic neutropenia", "neutropenia cyclic", "Cyclic Neutropenia", "LEUKOPENIA, CYCLIC", "NEUTROPENIA, CYCLIC", "neutropenia, cyclic", "Neutropenia, cyclic", "Cyclic hematopoiesis", "cyclic hematopoiesis", "periodic neutropenia", "Periodic neutropenia", "PERIODIC NEUTROPENIA", "Periodic Neutropenia", "neutropenia periodic", "cyclical neutropenia", "CYCLIC HEMATOPOIESIS", "Cyclic Hematopoiesis", "Cyclical neutropenia", "Cyclic haematopoiesis", "Neutropenia, periodic", "Cyclical neutropaenia", "neutropenia, periodic", "cyclic agranulocytosis", "Cyclic Agranulocytosis", "AGRANULOCYTOSIS, CYCLIC", "dysplasia, myelocytic periodic", "Dysplasia, Myelocytic Periodic", "DYSPLASIA, MYELOCYTIC PERIODIC", "cyclic neutropenia (diagnosis)", "Cyclical neutropenia (disorder)", "cyclic hematopoiesis (diagnosis)", "periodic neutropenia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cyclic hematopoiesis", "shortest_name_length": 2}
{"curie": "MONDO:0010477", "names": ["OHDOX", "BMRS, MKB type", "X-linked Ohdo syndrome", "OHDO SYNDROME, X-LINKED", "Ohdo syndrome, X-linked", "BMRS, Maat-Kievit-Brunner type", "Ohdo syndrome, Maat-Kievit-Brunner type", "Ohdo syndrome, X-linked, X-linked recessive", "Blepharophimosis-intellectual disability syndrome, MKB type", "blepharophimosis - intellectual disability syndrome, MKB type", "BLEPHAROPHIMOSIS-MENTAL RETARDATION SYNDROME, MAAT-KIEVIT-BRUNNER TYPE", "blepharophimosis-mental retardation syndrome, Maat-Kievit-Brunner type", "Blepharophimosis-mental retardation syndrome, Maat-Kievit-Brunner type", "Blepharophimosis-intellectual disability syndrome Maat-Kievit-Brunner type", "Blepharophimosis-intellectual disability syndrome, Maat-Kievit-Brunner type", "blepharophimosis-intellectual disability syndrome, Maat-Kievit-Brunner type", "blepharophimosis and intellectual disability syndrome, Maat-Kievit-Brunner type", "Blepharophimosis-intellectual disability syndrome Maat-Kievit-Brunner type (disorder)", "blepharophimosis and intellectual disability syndrome, Maat-Kievit-Brunner type (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blepharophimosis - intellectual disability syndrome, MKB type", "shortest_name_length": 5}
{"curie": "UMLS:C1334718", "names": ["metastatic PNET", "metastatic pPNET", "PNET, metastatic", "pPNET, metastatic", "metastatic Ewing sarcoma/PNET", "metastatic Ewing's sarcoma/PNET", "metastatic peripheral neuroepithelioma", "neuroepithelioma, metastatic, peripheral", "metastatic peripheral neuroectodermal tumor", "peripheral neuroectodermal tumor, metastatic", "metastatic primitive neuroectodermal tumor (PNET)", "primitive neuroectodermal tumor (PNET), metastatic", "metastatic Ewing sarcoma/primitive neuroectodermal tumor", "metastatic Ewing's sarcoma/primitive neuroectodermal tumor", "Metastatic Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor", "metastatic Ewing sarcoma/peripheral primitive neuroectodermal tumor", "Metastatic Ewing's Sarcoma/Peripheral Primitive Neuroectodermal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor", "shortest_name_length": 15}
{"curie": "MONDO:0019129", "names": ["global developmental delay-osteopenia-ectodermal defect syndrome", "Global developmental delay-osteopenia-ectodermal defect syndrome", "Global developmental delay, osteopenia, ectodermal defect syndrome", "Global developmental delay, osteopenia, ectodermal defect syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "global developmental delay-osteopenia-ectodermal defect syndrome", "shortest_name_length": 64}
{"curie": "MONDO:0010829", "names": ["CARASIL", "Maeda syndrome", "Nemoto disease", "Nemoto Disease", "MAEDA Syndrome", "MAEDA SYNDROME", "CARASIL syndrome", "SUBCORTICAL VASCULAR ENCEPHALOPATHY, PROGRESSIVE", "Subcortical Vascular Encephalopathy, Progressive", "subcortical vascular encephalopathy, progressive", "Cerebrovascular Disease with Thin Skin, Alopecia, and Disc Disease", "CEREBROVASCULAR DISEASE WITH THIN SKIN, ALOPECIA, AND DISC DISEASE", "cerebrovascular disease with thin skin, alopecia, and disc disease", "Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy", "Cerebral autosomal recessive arteriopathy with subcortical infarcts and leucoencephalopathy", "Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy", "Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy", "cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy", "CEREBRAL ARTERIOPATHY, AUTOSOMAL RECESSIVE, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY", "cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy", "Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)", "Familial Young-Adult-Onset Arteriosclerotic Leukoencephalopathy with Alopecia and Lumbago without Arterial Hypertension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CARASIL syndrome", "shortest_name_length": 7}
{"curie": "UMLS:C0162504", "names": ["Neutrophilic eccrine hidradenitis", "neutrophilic eccrine hidradenitis", "eccrine hidradenitis neutrophilic", "Neutrophilic Eccrine Hidradenitis", "Eccrine Hidradenitis, Neutrophilic", "Hidradenitis, Neutrophilic Eccrine", "Neutrophilic Eccrine Hidradenitides", "Hidradenitides, Neutrophilic Eccrine", "Eccrine Hidradenitides, Neutrophilic", "Neutrophilic eccrine hidradenitis (disorder)", "neutrophilic eccrine hidradenitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neutrophilic Eccrine Hidradenitis", "shortest_name_length": 33}
{"curie": "UMLS:C1512434", "names": ["High-Grade Papillary Urothelial Carcinoma", "Bladder Non-Invasive Papillary Urothelial Carcinoma, High Grade", "Non-Invasive Bladder Papillary Urothelial Carcinoma, High Grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder Non-Invasive Papillary Urothelial Carcinoma, High Grade", "shortest_name_length": 41}
{"curie": "UMLS:C1557989", "names": ["Kidney Perforation", "Kidney perforation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kidney perforation", "shortest_name_length": 18}
{"curie": "MONDO:0005650", "names": ["arenavirus infection", "infection, arenavirus", "arenavirus infections", "infections, arenavirus", "Arenaviridae infection", "Arenaviridae Infection", "Infection, Arenaviridae", "infection, Arenaviridae", "Arenaviridae Infections", "Infections, Arenaviridae", "infections, Arenaviridae", "disease due to arenavirus", "Disease due to Arenavirus", "DISEASES DUE TO ARENAVIRIDAE", "Disease caused by Arenavirus", "disease caused by arenavirus", "arenavirus infectious disease", "Disease due to Arenavirus, NOS", "Arenaviridae infectious disease", "Arenaviridae disease or disorder", "Disease caused by Arenavirus (disorder)", "Arenaviridae caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arenaviridae infectious disease", "shortest_name_length": 20}
{"curie": "MONDO:0020542", "names": ["Androblastoma", "Arrhenoblastoma", "virilizing ovarian tumor", "ovarian virilizing tumor", "Virilizing ovarian tumor", "Virilising ovarian tumour", "ovarian Sertoli-Leydig cell cancer", "Virilizing ovarian tumor (disorder)", "ovarian virilizing tumor (diagnosis)", "ovarian malignant Sertoli-Leydig cell tumor", "malignant ovarian sertoli-Leydig cell tumor", "malignant ovarian Sertoli-Leydig cell tumor", "ovarian Sertoli-Leydig cell tumor, malignant", "malignant Sertoli-Leydig cell tumor of ovary", "ovarian sertoli-Leydig cell tumor, malignant", "malignant Sertoli-Leydig cell tumor of the ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant Sertoli-Leydig cell tumor of ovary", "shortest_name_length": 13}
{"curie": "MONDO:0002317", "names": ["dizzy", "woozy", "DIZZY", "Woozy", "Dizzy", "vertigo", "VERTIGO", "Vertigo", "dizzying", "Vertigos", "wooziness", "dizziness", "Dizzyness", "giddiness", "Dizziness", "DIZZINESS", "WOOZINESS", "Vertigo NOS", "Dizzy spell", "Vertigo, NOS", "labrynthitis", "HEAD SPINNING", "head spinning", "Head spinning", "Rotary vertigo", "Lightheadedness", "Rotation of self", "vertigo; central", "Rotatory vertigo", "central; vertigo", "syndrome; vertigo", "vertigo; syndrome", "vertigo (symptom)", "Dizziness - giddy", "Vertigo (finding)", "spinning sensation", "Subjective vertigo", "SPINNING SENSATION", "VERTIGO CNS ORIGIN", "Spinning Sensation", "spinning dizziness", "VERTIGO SUBJECTIVE", "Vertigo CNS origin", "Subjective Vertigo", "Spinning sensation", "Systematic vertigo", "CNS Origin Vertigo", "Vertigo subjective", "Vertigo, CNS Origin", "Sensation, Spinning", "Vertigo, Subjective", "Subjective Vertigos", "Spinning Sensations", "dizziness (symptom)", "CNS Origin Vertigos", "Dizziness (finding)", "Origin Vertigo, CNS", "vertigo (diagnosis)", "Vertigos, Subjective", "Sensations, Spinning", "Head revolving round", "Vertigos, CNS Origin", "Origin Vertigos, CNS", "HEAD REVOLVING AROUND", "Head revolving around", "central origin vertigo", "VERTIGO CENTRAL ORIGIN", "Central Origin Vertigo", "Origin Vertigo, Central", "Feel I'm spinning round", "Vertigo, Central Origin", "Dizziness and giddiness", "Central Origin Vertigos", "Origin Vertigos, Central", "Vertigos, Central Origin", "vertigo of central origin", "Vertigo of central origin", "central vestibular vertigo", "Central vestibular vertigo", "Vertigo (spinning sensation)", "Subjective vertigo (finding)", "Dizziness and giddiness symptoms", "Dizziness and giddiness (finding)", "Vertigo of central origin (disorder)", "central nervous system origin vertigo", "vertigo of central origin (diagnosis)", "Vertigo central nervous system origin", "Central Nervous System Origin Vertigo", "Vertigo, Central Nervous System Origin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system origin vertigo", "shortest_name_length": 5}
{"curie": "UMLS:C5205729", "names": ["Prostate Undifferentiated Pleomorphic Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Undifferentiated Pleomorphic Sarcoma", "shortest_name_length": 45}
{"curie": "MONDO:0019308", "names": ["EBJ-I", "JEB-I", "JEB inversa", "inverse JEB", "Junctional epidermolysis bullosa inversa", "junctional epidermolysis bullosa inversa", "Epidermolysis bullosa inversa dystrophica"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "junctional epidermolysis bullosa inversa", "shortest_name_length": 5}
{"curie": "MONDO:0024475", "names": ["SIL", "SIN", "sil", "sils", "squamous intraepithelial lesion", "Squamous intraepithelial lesion", "Squamous Intraepithelial Lesion", "intraepithelial squamous lesion", "Squamous Intraepithelial Lesions", "Intraepithelial Lesion, Squamous", "intraepithelial lesions squamous", "Lesions, Squamous Intraepithelial", "Squamous intraepithelial lesion, NOS", "Squamous Cell Intraepithelial Neoplasia", "squamous cell intraepithelial neoplasia", "Squamous intraepithelial lesion (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "squamous cell intraepithelial neoplasia", "shortest_name_length": 3}
{"curie": "MONDO:0001979", "names": ["dump syndrome", "Jejunal syndrome", "dumping syndrome", "DUMPING SYNDROME", "Dumping syndrome", "syndrome dumping", "jejunal syndrome", "Dumping Syndrome", "dumping; syndrome", "Syndrome, Dumping", "Dumping Syndromes", "syndrome; dumping", "Syndromes, Dumping", "Post-cibal syndrome", "Dumping (jejunal) syndrome", "dumping (jejunal) syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dumping syndrome", "shortest_name_length": 13}
{"curie": "UMLS:C3495445", "names": ["Toxoplasma Pneumonia", "pneumonia; toxoplasmosis (manifestation)", "toxoplasmosis; pneumonia (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Toxoplasma Pneumonia", "shortest_name_length": 20}
{"curie": "MONDO:0004059", "names": ["sensitive dentin", "Sensitive dentin", "sensitivity teeth", "teeth sensitivity", "Teeth Sensitivity", "Tooth Sensitivity", "dentin; sensitive", "tooth sensitivity", "Tooth sensitivity", "sensitive; dentin", "sensitivity tooth", "Sensitivity, Tooth", "dentin sensitivity", "Dentin Sensitivity", "dentin; sensitivity", "Sensitivity, Dentin", "Tooth Sensitivities", "Dentine sensitivity", "Dentine Sensitivity", "Sensitivity, Dentine", "Sensitivity of teeth", "Sensitivity of Teeth", "Sensitivity Of Tooth", "Sensitivities, Tooth", "Dentin Sensitivities", "Sensitivities, Dentin", "Dentine Sensitivities", "tooth hypersensitivity", "Tooth hypersensitivity", "Sensitivities, Dentine", "dentin hypersensitivity", "Dentin Hypersensitivity", "Dentine hypersensitivity", "Dentine Hypersensitivity", "dentine hypersensitivity", "Hypersensitivity, Dentin", "Hypersensitivity, Dentine", "Dentin Hypersensitivities", "Hypersensitivities, Dentin", "Dentine Hypersensitivities", "Hypersensitivities, Dentine", "Sensitive dentin (disorder)", "sensitive dentin (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dentin sensitivity", "shortest_name_length": 16}
{"curie": "UMLS:C0239816", "names": ["eczema hand", "hand eczema", "Hand eczema", "eczema hands", "HAND DERMATITIS", "hand dermatitis", "Hand dermatitis", "dermatitis hand", "dermatitis hands", "Dermatitis of hand", "Hand eczema (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hand eczema", "shortest_name_length": 11}
{"curie": "MONDO:0014730", "names": ["MCPH16", "primary autosomal recessive microcephaly 16", "MICROCEPHALY 16, PRIMARY, AUTOSOMAL RECESSIVE", "microcephaly 16, primary, autosomal recessive", "microcephaly 16, primary, autosomal recessive; MCPH16"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly 16, primary, autosomal recessive", "shortest_name_length": 6}
{"curie": "MONDO:0006564", "names": ["irritant dermatitis", "Irritant Dermatitis", "irritant; dermatitis", "Dermatitis, Irritant", "dermatitis; irritant", "dermatitis irritants", "Irritant Dermatitides", "Dermatitides, Irritant", "Irritant contact dermatitis", "dermatitis contact irritant", "irritant contact dermatitis", "contact dermatitis irritant", "primary irritant dermatitis", "Primary irritant dermatitis", "Irritant Contact Dermatitis", "Dermatitis irritant contact", "Primary Irritant Dermatitis", "Dermatitis, Primary Irritant", "Irritant Dermatitis, Primary", "contact; dermatitis, irritant", "Primary Irritant Dermatitides", "dermatitis; contact, irritant", "Dermatitides, Primary Irritant", "Irritant Dermatitides, Primary", "Non-allergic contact dermatitis", "ICD - Irritant contact dermatitis", "Irritant contact dermatitis (disorder)", "irritant contact dermatitis (diagnosis)", "Irritant contact dermatitis, unspecified cause"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "irritant dermatitis", "shortest_name_length": 19}
{"curie": "UMLS:C1696155", "names": ["vaginal perforation", "Vaginal perforation", "Vaginal Perforation", "vaginal perforation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Perforation", "shortest_name_length": 19}
{"curie": "MONDO:0006644", "names": ["Laennec", "Portal Cirrhosis", "Portal cirrhosis", "cirrhosis portal", "portal cirrhosis", "alcohol; Laennec", "laennec cirrhosis", "portal; cirrhosis", "cirrhosis; portal", "CIRRHOSIS, LAENNEC", "alcohol; cirrhosis", "LAENNECS CIRRHOSIS", "Laennec; cirrhosis", "Laennec; alcoholic", "cirrhosis; Laennec", "laennecs cirrhosis", "Cirrhosis alcoholic", "Alcoholic cirrhosis", "Alcoholic Cirrhosis", "ALCOHOLIC CIRRHOSIS", "laennec's cirrhosis", "alcoholic cirrhosis", "cirrhosis laennec's", "Laennec's cirrhosis", "CIRRHOSIS, ALCOHOLIC", "cirrhosis; alcoholic", "Cirrhosis, Laennec's", "Cirrhosis, alcoholic", "cirrhosis laennecs's", "PC - Portal cirrhosis", "Portal cirrhosis, NOS", "liver cirrhosis portal", "Alcoholic cirrhosis NOS", "LIVER, CIRRHOSIS, PORTAL", "Alcoholic Liver Cirrhosis", "CIRRHOSIS ALCOHOL INDUCED", "Alcoholic liver cirrhosis", "cirrhosis alcoholic liver", "alcohol induced cirrhosis", "alcoholic liver cirrhosis", "alcoholic cirrhosis liver", "Liver Cirrhosis, Alcoholic", "Portal cirrhosis (of liver)", "liver; cirrhosis, alcoholic", "Portal cirrhosis (disorder)", "Alcoholic Hepatic Cirrhosis", "cirrhosis; liver, alcoholic", "Portal cirrhosis (diagnosis)", "Hepatic Cirrhosis, Alcoholic", "Alcoholic cirrhosis of liver", "alcoholic cirrhosis of liver", "of alcoholic liver cirrhosis", "cirrhosis; Laennec, alcoholic", "MICRONODAL CIRRHOSIS LAENNECS", "Laennec; cirrhosis, alcoholic", "alcoholic cirrhosis laennec's", "Laennec's cirrhosis, alcoholic", "Alcoholic cirrhosis (disorder)", "MICRONODAL CIRRHOSIS <LAENNECS>", "alcoholic cirrhosis (diagnosis)", "Cirrhosis of the Liver Secondary to Alcohol Use"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alcoholic liver cirrhosis", "shortest_name_length": 7}
{"curie": "MONDO:0014107", "names": ["HH21", "FLRT3 hypogonadotropic hypogonadism", "hypogonadotropic hypogonadism 21 with anosmia", "HYPOGONADOTROPIC HYPOGONADISM 21 WITH OR WITHOUT ANOSMIA", "hypogonadotropic hypogonadism 21 with or without anosmia", "hypogonadotropic hypogonadism caused by mutation in FLRT3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadotropic hypogonadism 21 with or without anosmia", "shortest_name_length": 4}
{"curie": "UMLS:C4763824", "names": ["Pediatric Cystic Nephroma", "Childhood Cystic Nephroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Cystic Nephroma", "shortest_name_length": 25}
{"curie": "MONDO:0016221", "names": ["temporomandibular joint anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "temporomandibular joint anomaly", "shortest_name_length": 31}
{"curie": "UMLS:C1370508", "names": ["Intracranial Germ Cell Tumor", "Adult Intracranial Germ Cell Tumor", "adult intracranial germ cell tumor", "intracranial germ cell tumors, adult", "germ cell tumors, adult intracranial", "tumors, adult intracranial germ cell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Intracranial Germ Cell Tumor", "shortest_name_length": 28}
{"curie": "MONDO:0041403", "names": ["toxic amblyopia", "Amblyopia tobacco", "tobacco amblyopia", "Tobacco amblyopia", "amblyopia; tobacco", "tobacco; amblyopia", "Amblyopia, tobacco", "Smoker's blindness", "Tobacco amblyopia (disorder)", "nutritional optic neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "toxic amblyopia", "shortest_name_length": 15}
{"curie": "UMLS:C0686402", "names": ["Metastatic Tumor to the Brainstem", "Metastatic Tumor to the Brain Stem", "Metastatic Neoplasm to the Brainstem", "Metastatic Neoplasm to the Brain Stem", "secondary malignant neoplasm brain stem", "Secondary malignant neoplasm of brain stem", "Metastatic malignant neoplasm of brain stem", "Metastatic malignant neoplasm to brain stem", "Metastatic Malignant Neoplasm in the Brain Stem", "Metastatic Malignant Neoplasm to the Brain Stem", "Secondary malignant neoplasm of brain stem (diagnosis)", "Metastatic malignant neoplasm to brain stem (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to brain stem", "shortest_name_length": 33}
{"curie": "UMLS:C3640090", "names": ["Respiratory Failure due to CNS Disorder", "Respiratory Failure due to Central Nervous System Disorder", "Respiratory Failure Related to Central Nervous System Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Respiratory Failure Related to Central Nervous System Disorder", "shortest_name_length": 39}
{"curie": "UMLS:C1276076", "names": ["Infected atopic dermatitis", "Impetiginized atopic dermatitis", "impetiginized atopic dermatitis", "Impetiginized atopic dermatitis (disorder)", "impetiginized atopic dermatitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Impetiginized atopic dermatitis", "shortest_name_length": 26}
{"curie": "OMIM:613793", "names": [], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"]}
{"curie": "UMLS:C0267288", "names": ["Acute peptic ulcer with hemorrhage", "acute peptic ulcer with hemorrhage", "Peptic ulcer, acute with hemorrhage", "Acute peptic ulcer with haemorrhage", "Peptic ulcer, acute with haemorrhage", "ulcer; peptic, acute, with hemorrhage", "Acute peptic ulcer with hemorrhage (disorder)", "acute peptic ulcer with hemorrhage (diagnosis)", "Acute peptic ulcer, site unspecified, with hemorrhage", "Acute peptic ulcer of unspecified site with hemorrhage", "Acute peptic ulcer of unspecified site with haemorrhage", "Acute peptic ulcer of unspecified site with hemorrhage, without mention of obstruction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute peptic ulcer with hemorrhage", "shortest_name_length": 34}
{"curie": "MONDO:0800041", "names": ["MTTS2 MELAS syndrome", "MELAS syndrome caused by mutation in MTTS2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MELAS syndrome caused by mutation in MTTS2", "shortest_name_length": 20}
{"curie": "UMLS:C5668167", "names": ["Pericardial Primary Effusion Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pericardial Primary Effusion Lymphoma", "shortest_name_length": 37}
{"curie": "UMLS:C3274706", "names": ["Autoimmune Cytopenia", "Autoimmune cytopenia", "Autoimmune cytopenias"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Autoimmune cytopenia", "shortest_name_length": 20}
{"curie": "MONDO:0015358", "names": ["HSMN", "HMSN", "hmsn", "Neuropathic Muscular Atrophy", "Neuropathic muscular atrophy", "neuropathic muscular atrophy", "CMT - Charcot-Marie-Tooth disease", "Hereditary sensorimotor neuropathy", "Hereditary Sensorimotor Neuropathy", "Hereditary sensory-motor neuropathy", "HEREDITARY SENSORY MOTOR NEUROPATHY", "Hereditary Sensory-Motor Neuropathies", "Herditary Sensory and Motor Neuropathy", "Hereditary Motor and Sensory Neuropathy", "Hereditary Sensory and Motor Neuropathy", "Hereditary motor and sensory neuropathy", "Hereditary sensory and motor neuropathy", "hereditary motor and sensory neuropathy", "Hereditary sensory-motor neuropathy, NOS", "neuropathy; hereditary, motor and sensory", "Hereditary Motor and Sensory Neuropathies", "sensory and motor; neuropathic, hereditary", "hereditary; neuropathic, motor and sensory", "Neuropathies, Hereditary Motor and Sensory", "HSMN - Hereditary sensory and motor neuropathy", "HMSN - Hereditary motor and sensory neuropathy", "hereditary motor and sensory neuropathies (HMSN)", "Hereditary motor and sensory neuropathy (disorder)", "hereditary motor and sensory neuropathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary motor and sensory neuropathy", "shortest_name_length": 4}
{"curie": "UMLS:C5204293", "names": ["Papillary-Basaloid Carcinoma of the Penis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Papillary-Basaloid Carcinoma of the Penis", "shortest_name_length": 41}
{"curie": "UMLS:C1708106", "names": ["Functional Pancreatic Neuroendocrine Tumor G2", "Functioning Pancreatic Neuroendocrine Tumor G2", "Functioning Well Differentiated Pancreatic Endocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Functioning Pancreatic Neuroendocrine Tumor G2", "shortest_name_length": 45}
{"curie": "UMLS:C0729518", "names": ["Bacterial respiratory infection", "respiratory bacterial infection", "respiratory infection bacterial", "bacterial respiratory infection", "bacterial infections respiratory", "Bacterial respiratory infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bacterial respiratory infection", "shortest_name_length": 31}
{"curie": "MONDO:0017870", "names": ["supravalvular pulmonary stenosis", "pulmonary supravalvular stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "supravalvular pulmonary stenosis", "shortest_name_length": 32}
{"curie": "MONDO:0019159", "names": ["Loffler's myocarditis", "Loeffler endocarditis", "endocarditis; Löffler", "Löffler; endocarditis", "Loffler's endocarditis", "Löffler's endocarditis", "loffler's endocarditis", "eosinophilic endocarditis", "constrictive endocarditis", "Constrictive endocarditis", "Eosinophilic Endomyocardial disease", "Eosinophilic Endomyocardial Disease", "eosinophilic endomyocardial disease", "Eosinophilic endomyocardial disease", "Endomyocardial (eosinophilic) disease", "endomyocardial; disease (eosinophilic)", "Löffler's parietal fibroplastic endocarditis", "Loffler's parietal fibroplastic endocarditis", "Endomyocardiopathy with eosinophilia syndrome", "Primary eosinophilic endomyocardial restrictive cardiomyopathy", "Primary eosinophilic endomyocardial restrictive cardiomyopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Loeffler endocarditis", "shortest_name_length": 21}
{"curie": "UMLS:C5555052", "names": ["EWSR1-NFATC2 Sarcoma", "EWSR1::NFATC2 Sarcoma", "Round Cell Sarcoma with EWSR1-NFATC2 Gene Fusion", "Round Cell Sarcoma with EWSR1::NFATC2 Gene Fusion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Round Cell Sarcoma with EWSR1-NFATC2 Gene Fusion", "shortest_name_length": 20}
{"curie": "UMLS:C0158454", "names": ["fracture malunion", "Fracture malunion", "Fracture Malunion", "Fracture;malunion", "Malunion, Fracture", "fracture; malunion", "Fracture Malunions", "Malunited Fracture", "Malunions, Fracture", "Fracture, Malunited", "Malunited Fractures", "Fractures, Malunited", "Malunion of fracture", "malunion of fracture", "Fracture, Abnormal Union", "union; fracture, malunion", "Fractures, Abnormal Union", "Malunion of fracture, NOS", "Fracture malunion (disorder)", "malunion of fracture (diagnosis)", "Malunion of fracture, site unspecified", "Malunion of fracture (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malunited Fracture", "shortest_name_length": 17}
{"curie": "UMLS:C0341750", "names": ["bladder hemorrhage", "Bladder hemorrhage", "Bladder haemorrhage", "hemorrhage; bladder", "bladder; hemorrhage", "Urinary bladder bleeding", "HEMORRHAGE URINARY BLADDER", "Urinary Bladder Hemorrhage", "Urinary bladder hemorrhage", "Hemorrhage urinary bladder", "Haemorrhage urinary bladder", "Urinary bladder haemorrhage", "Bladder hemorrhage (disorder)", "bladder hemorrhage (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder hemorrhage", "shortest_name_length": 18}
{"curie": "MONDO:0006459", "names": ["thymoma type B1", "Thymoma Type B1", "type b1 thymoma", "type B1 thymoma", "Organoid Thymoma", "organoid thymoma", "thymoma, organoid", "Thymoma, organoid", "lymphocytic thymoma", "Thymoma, type B1, NOS", "Lymphocyte-Rich Thymoma", "lymphocyte-rich thymoma", "type B1 thymoma (diagnosis)", "lymphocyte-predominant thymoma", "Predominantly Cortical Thymoma", "predominantly cortical thymoma", "Lymphocyte-Predominant Thymoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thymoma type B1", "shortest_name_length": 15}
{"curie": "MONDO:0008004", "names": ["PMV", "MVP", "MVP PROLAPSED MITRAL VALVE", "familial mitral valve prolapse", "mitral valve prolapse familial", "Familial mitral valve prolapse", "MITRAL VALVE PROLAPSE, FAMILIAL", "mitral valve prolapse, familial", "Familial mitral valve prolapse (disorder)", "hereditary mitral valve prolapse (disease)", "Familial mitral valve prolapse (diagnosis)", "mitral valve prolapse, familial, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial mitral valve prolapse", "shortest_name_length": 3}
{"curie": "UMLS:C0343337", "names": ["Pseudomonas gastrointestinal tract infection", "Pseudomonas gastrointestinal tract infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pseudomonas gastrointestinal tract infection", "shortest_name_length": 44}
{"curie": "MONDO:0011104", "names": ["CCA2", "CTRCT3", "cataract 3 multiple types", "CRYBB2 cataract (disease)", "CATARACT 3, MULTIPLE TYPES", "cataract 3, multiple types", "congenital Cerulean type cataract 2", "congenital cerulean type cataract 2", "CATARACT, CONGENITAL, CERULEAN TYPE, 2", "Cataract, Congenital, Blue Dot Type, 2", "Cataract, Congenital, Cerulean Type, 2", "cataract, congenital, cerulean type, 2", "cataract (disease) caused by mutation in CRYBB2", "cataract 3 multiple types with or without microcornea", "cataract 3, multiple types, with or without microcornea", "CATARACT 3, MULTIPLE TYPES, WITH OR WITHOUT MICROCORNEA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 3 multiple types", "shortest_name_length": 4}
{"curie": "MONDO:0032809", "names": ["FVH", "HEPATITIS, FULMINANT VIRAL, SUSCEPTIBILITY TO", "hepatitis, fulminant viral, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatitis, fulminant viral, susceptibility to", "shortest_name_length": 3}
{"curie": "MONDO:0000652", "names": ["integumental system benign neoplasm", "integumentary system benign neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "integumentary system benign neoplasm", "shortest_name_length": 35}
{"curie": "MONDO:0001925", "names": ["Retinal dystrophy in systemic or cerebroretinal lipidoses", "retinal dystrophy in systemic or cerebroretinal lipidoses", "retinal dystrophy in systemic or cerebroretinal lipidoses (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal dystrophy in systemic or cerebroretinal lipidoses", "shortest_name_length": 57}
{"curie": "MONDO:0011235", "names": ["Ray-Peterson-Scott syndrome", "Pelvic dysplasia arthrogryposis of lower limbs", "pelvic dysplasia arthrogryposis of lower limbs", "pelvic hypoplasia with lower limb arthrogryposis", "pelvic hypoplasia with LOWER-limb arthrogryposis", "PELVIC HYPOPLASIA WITH LOWER-LIMB ARTHROGRYPOSIS", "Pelvic Hypoplasia with Lower-Limb Arthrogryposis", "Pelvic hypoplasia with lower limb arthrogryposis", "Pelvic hypoplasia with arthrogryposis of lower limbs", "pelvic hypoplasia with arthrogryposis of lower limbs", "pelvic dysplasia-arthrogryposis of lower limbs syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pelvic dysplasia-arthrogryposis of lower limbs syndrome", "shortest_name_length": 27}
{"curie": "MONDO:0017425", "names": ["preaxial polydactyly of hand", "preaxial polydactyly of fingers"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "preaxial polydactyly of fingers", "shortest_name_length": 28}
{"curie": "UMLS:C4054407", "names": ["Nephropathy due to Aminoglycosides"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephropathy due to Aminoglycosides", "shortest_name_length": 34}
{"curie": "UMLS:C4525618", "names": ["Stage IV Duodenal Neuroendocrine Tumor", "Stage IV Duodenal Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Duodenal Neuroendocrine Tumor AJCC v8", "shortest_name_length": 38}
{"curie": "MONDO:0010216", "names": ["XP7", "XPG", "XPGC", "XP-G", "Xpg-Cs", "XPG/CS", "XP group G", "XP, GROUP G", "XP, Group G", "xeroderma pigmentosum 7", "Xeroderma Pigmentosum VII", "XERODERMA PIGMENTOSUM VII", "xeroderma pigmentosum VII", "ERCC5 xeroderma pigmentosum", "xeroderma pigmentosum type 7", "Xeroderma Pigmentosum Group G", "Xeroderma pigmentosum group G", "xeroderma pigmentosum group G", "xeroderma pigmentosum, group G", "Xeroderma pigmentosum, group G", "xeroderma pigmentosum group type G", "Xeroderma pigmentosum, group G (disorder)", "xeroderma pigmentosum complementation group G", "Xeroderma Pigmentosum, Complementation Group G", "XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G", "xeroderma pigmentosum, complementation group G", "XERODERMA PIGMENTOSUM, TYPE G/COCKAYNE SYNDROME", "Xeroderma Pigmentosum, Type G-Cockayne Syndrome", "xeroderma pigmentosum, type G/Cockayne syndrome", "xeroderma pigmentosum, group G/Cockayne syndrome", "xeroderma pigmentosum caused by mutation in ERCC5", "xeroderma pigmentosum, complementation group type G"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "xeroderma pigmentosum group G", "shortest_name_length": 3}
{"curie": "MONDO:0018831", "names": ["HTRA1-related cerebral angiopathy", "HTRA1-related cerebral small vessel disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HTRA1-related cerebral small vessel disease", "shortest_name_length": 33}
{"curie": "UMLS:C0854572", "names": ["sinus perforation", "Sinus perforation", "Sinus Perforation", "perforation; sinus", "sinus; perforation", "perforations sinus", "Perforation of sinus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinus perforation", "shortest_name_length": 17}
{"curie": "MONDO:0007872", "names": ["LADD", "LADD1", "LADD syndrome", "LADD SYNDROME", "lard syndrome", "LARD syndrome", "LADD1 SYNDROME", "LEVY-HOLLISTER SYNDROME", "Levy-Hollister syndrome", "Levy Hollister syndrome", "Levy-Hollister Syndrome", "Levy-Hollister syndrome (disorder)", "Lacrimoauriculoradiodental syndrome", "LACRIMOAURICULODENTODIGITAL SYNDROME", "lacrimoauriculodentodigital syndrome", "LACRIMOAURICULODENTODIGITAL syndrome", "Lacrimoauriculodentodigital syndrome", "Lacrimoauriculodento-digital syndrome", "lacrimoauriculodentodigital syndrome 1", "LACRIMOAURICULODENTODIGITAL SYNDROME 1", "Lacrimo-auriculo-dento-digital syndrome", "Lacrimo-auriculo-dento-digital syndrome 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "LADD syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0009711", "names": ["CFTD", "CFTDM", "congenital myopathy 4A", "Fiber type disproportion", "Fiber-type disproportion", "fibre-type; disproportion", "disproportion; fibre-type", "congenital fiber type disproportion", "Congenital Fiber Type Disproportion", "Congenital fiber type disproportion", "Congenital Fiber-Type Disproportion", "congenital fiber-type disproportion", "Disproportion, Congenital Fiber-Type", "Congenital Fiber-Type Disproportions", "Fiber-Type Disproportion, Congenital", "Disproportions, Congenital Fiber-Type", "Fiber-Type Disproportions, Congenital", "Congenital Fiber-Type Disproportion Myopathy", "Congenital fiber type disproportion myopathy", "Congenital fiber-type disproportion myopathy", "congenital fiber-type disproportion myopathy", "Fiber-Type Disproportion Myopathy, Congenital", "Fiber Type Disproportion Myopathy, Congenital", "FIBER-TYPE DISPROPORTION MYOPATHY, CONGENITAL", "Congenital myopathy with fibre type disproportion", "congenital myopathy with fiber type disproportion", "Congenital Myopathy with Fiber Type Disproportion", "congenital myopathy with fibre type disproportion", "Congenital myopathy with fiber type disproportion", "myopathy, congenital with fiber-type disproportion", "Myopathy, Congenital, With Fiber-Type Disproportion", "MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION", "Congenital myopathy with fiber type disproportion (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital fiber-type disproportion myopathy", "shortest_name_length": 4}
{"curie": "UMLS:C5237029", "names": ["Metastatic Malignant Mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Malignant Mesothelioma", "shortest_name_length": 33}
{"curie": "UMLS:C1519833", "names": ["Urinary Tract Precancerous Condition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urinary Tract Precancerous Condition", "shortest_name_length": 36}
{"curie": "MONDO:0020805", "names": ["benign basal cell tumor", "Benign basal cell tumor", "Benign Basal Cell Tumor", "Benign basal cell tumour", "benign basal cell neoplasm", "Benign Basal Cell Neoplasm", "Benign basal cell tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign basal cell neoplasm", "shortest_name_length": 23}
{"curie": "MONDO:0015854", "names": ["polymastia", "accessory breasts", "supernumerary breasts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "supernumerary breasts", "shortest_name_length": 10}
{"curie": "MONDO:0015089", "names": ["autosomal recessive complex SPG", "autosomal recessive complex HSP", "autosomal recessive complicated SPG", "autosomal recessive complicated HSP", "autosomal recessive complex spastic paraplegia", "autosomal recessive complicated spastic paraplegia", "autosomal recessive complex hereditary spastic paraplegia", "complex hereditary spastic paraplegia, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive complex spastic paraplegia", "shortest_name_length": 31}
{"curie": "UMLS:C1336523", "names": ["Submaxillary Gland Carcinoma ex Pleomorphic Adenoma", "Submandibular Gland Carcinoma ex Pleomorphic Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Submandibular Gland Carcinoma ex Pleomorphic Adenoma", "shortest_name_length": 51}
{"curie": "MONDO:0016757", "names": ["MTT", "Malignant triton tumor", "Malignant Triton Tumor", "malignant triton tumor", "Malignant Triton tumor", "malignant Triton tumour", "Malignant Triton tumour", "Triton tumor, malignant", "Triton tumour, malignant", "MPNST with Rhabdomyosarcoma", "[M] Triton tumor, malignant", "MPNST with rhabdomyosarcoma", "[M] Triton tumour, malignant", "Malignant Triton tumor (disorder)", "malignant triton tumor (diagnosis)", "MPNST with rhabdomyoblastic differentiation", "MPNST with rhabdomyosarcomatous differentiation", "Malignant Schwannoma with rhabdomyoblastic differentiation", "Malignant schwannoma with rhabdomyoblastic differentiation", "Malignant neurilemmoma with rhabdomyoblastic differentiation", "malignant peripheral nerve sheath tumor with rhabdomyosarcoma", "Malignant Peripheral Nerve Sheath Tumor with Rhabdomyosarcoma", "malignant peripheral nerve sheath neoplasm with rhabdomyosarcoma", "Malignant Peripheral Nerve Sheath Neoplasm with Rhabdomyosarcoma", "Malignant Tumor of Peripheral Nerve Sheath with Rhabdomyosarcoma", "malignant tumor of peripheral nerve sheath with rhabdomyosarcoma", "malignant neoplasm of peripheral nerve sheath with rhabdomyosarcoma", "Malignant Neoplasm of Peripheral Nerve Sheath with Rhabdomyosarcoma", "malignant tumor of the peripheral nerve sheath with rhabdomyosarcoma", "Malignant Tumor of the Peripheral Nerve Sheath with Rhabdomyosarcoma", "malignant neoplasm of the peripheral nerve sheath with rhabdomyosarcoma", "Malignant Neoplasm of the Peripheral Nerve Sheath with Rhabdomyosarcoma", "Malignant peripheral nerve sheath tumor with rhabdomyoblastic differentiation", "Malignant peripheral nerve sheath tumour with rhabdomyoblastic differentiation", "malignant peripheral nerve sheath tumor with rhabdomyosarcomatous differenciation", "Malignant peripheral nerve sheath tumor with rhabdomyosarcomatous differenciation", "malignant peripheral nerve sheath tumor (MPNST) with rhabdomyoblastic differentiation", "malignant peripheral nerve sheath tumor (MPNST) with rhabdomyoblastic differentiation (diagnosis)", "Malignant peripheral nerve sheath tumor with rhabdomyoblastic differentiation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant triton tumor", "shortest_name_length": 3}
{"curie": "MONDO:0016455", "names": ["TS", "VATS", "pilomatrix dysplasia", "Pilomatrix dysplasia", "trichodysplasia spinulosa", "Trichodysplasia spinulosa", "Cyclosporine-induced folliculodystrophy", "virus-associated trichodysplasia spinulosa", "Virus-associated trichodysplasia spinulosa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "virus-associated trichodysplasia spinulosa", "shortest_name_length": 2}
{"curie": "MONDO:0017063", "names": ["total spina bifida aperta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "total spina bifida aperta", "shortest_name_length": 25}
{"curie": "UMLS:C2980042", "names": ["Stage IIIC Breast Cancer", "stage IIIC breast cancer", "Stage IIIC Breast Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Breast Cancer AJCC v7", "shortest_name_length": 24}
{"curie": "MONDO:0012429", "names": ["AGS2", "Aicardi-Goutieres Syndrome 2", "Aicardi-Goutieres syndrome 2", "AICARDI-GOUTIERES SYNDROME 2", "Aicardi-Goutieres syndrome type 2", "RNASEH2B Aicardi-Goutieres syndrome", "RNASEH2B-related Aicardi-Goutieres syndrome", "Aicardi-Goutieres syndrome caused by mutation in RNASEH2B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aicardi-Goutieres syndrome 2", "shortest_name_length": 4}
{"curie": "UMLS:C1266006", "names": ["clear cell type squamous cell carcinoma", "Squamous cell carcinoma, clear cell type", "Squamous Cell Carcinoma, Clear Cell Type", "squamous cell carcinoma, clear cell type", "clear cell type squamous cell carcinoma (diagnosis)", "Squamous cell carcinoma, clear cell type (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Squamous cell carcinoma, clear cell type", "shortest_name_length": 39}
{"curie": "MONDO:0009054", "names": ["ARCL2", "ADCL2", "Arcl2", "ARCL2A", "ARCL2, Debré type", "ARCL2, Debre type", "ARCL2, classic type", "cutis laxa type IIA", "Cutis Laxa, Debre Type", "CUTIS LAXA, DEBRE TYPE", "Cutis Laxa With Bone Dystrophy", "Cutis laxa with osteodystrophy", "CUTIS LAXA WITH BONE DYSTROPHY", "Cutis laxa with bone dystrophy", "cutis laxa type IIA (diagnosis)", "Autosomal recessive cutis laxa type 2A", "Cutis Laxa, Autosomal Recessive, Type IIA", "CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA", "Cutis laxa with osteodystrophy (disorder)", "Cutis Laxa With Growth And Developmental Delay", "CUTIS LAXA WITH GROWTH AND DEVELOPMENTAL DELAY", "ARCL2A - autosomal recessive cutis laxa type 2A", "autosomal recessive cutis laxa type 2, Debre type", "Autosomal recessive cutis laxa type 2A (disorder)", "autosomal recessive cutis laxa type 2, Debré type", "autosomal recessive cutis laxa type 2, classic type", "autosomal recessive cutis laxa type II classic type", "CUTIS LAXA WITH CONGENITAL DISORDER OF GLYCOSYLATION", "CUTIS LAXA WITH JOINT LAXITY AND RETARDED DEVELOPMENT", "Cutis laxa with joint laxity AND retarded development", "Cutis laxa with joint laxity and retarded development", "Cutis Laxa With Joint Laxity And Retarded Development", "Cutis Laxa With Or Without Congenital Disorder Of Glycosylation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive cutis laxa type 2, classic type", "shortest_name_length": 5}
{"curie": "UMLS:C2981681", "names": ["stage IIB prostate cancer", "Stage IIB Prostate Cancer", "Stage IIB Prostate Cancer AJCC v7", "stage IIB prostate cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Prostate Cancer AJCC v7", "shortest_name_length": 25}
{"curie": "MONDO:0035679", "names": ["TS2", "LQT8 type 2", "Timothy syndrome type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Timothy syndrome type 2", "shortest_name_length": 3}
{"curie": "MONDO:0006227", "names": ["Gastric NET G1", "stomach NET G1", "gastric NET G1", "carcinoid gastric", "gastric carcinoid", "Gastric carcinoid", "carcinoids gastric", "gastric ECL cell NET", "Gastric ECL Cell NET", "gastric carcinoid tumor", "Gastric ECL Cell NET G1", "stomach carcinoid tumor", "carcinoid stomach tumor", "Gastric Carcinoid Tumor", "gastric ECL cell NET G1", "Carcinoid tumor of stomach", "Carcinoid tumour of stomach", "Carcinoid tumor of the stomach", "Gastric Neuroendocrine Tumor G1", "gastric neuroendocrine tumor G1", "Carcinoid tumour of the stomach", "Gastric ECL-Cell Carcinoid Tumor", "gastric neoplasm carcinoid tumor", "gastric ECL-cell carcinoid tumor", "stomach neuroendocrine neoplasm G1", "Carcinoid tumor of stomach (disorder)", "Carcinoid tumor of stomach (diagnosis)", "gastric ECL cell, histamine-producing NET", "Gastric ECL Cell, Histamine-Producing NET", "grade 1 neuroendocrine neoplasm of stomach", "gastric enterochromaffin-like cell carcinoid tumor", "Gastric Enterochromaffin-Like Cell Carcinoid Tumor", "gastric enterochromaffin-like cell neuroendocrine tumor", "Gastric Enterochromaffin-Like Cell Neuroendocrine Tumor", "stomach neuroendocrine tumor, well differentiated, low grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric neuroendocrine tumor G1", "shortest_name_length": 14}
{"curie": "MONDO:0016898", "names": ["Monosomy 20p", "deletion 20p", "20p deletion", "monosomy 20p", "20p monosomy", "Deletion 20p", "partial monosomy 20p", "chromosome 20p deletion", "Pure partial 20p deletion", "Chromosome 20, deletion 20p", "partial deletion of chromosome 20p", "partial monosomy of chromosome 20p", "partial monosomy of the short arm of chromosome 20", "partial deletion of the short arm of chromosome 20", "partial monosomy of the short arm of chromosome type 20"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial monosomy of the short arm of chromosome 20", "shortest_name_length": 12}
{"curie": "MONDO:0032628", "names": ["MC1DN24", "nuclear type mitochondrial complex I deficiency 24", "mitochondrial complex 1 deficiency, nuclear type 24", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 24"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 24", "shortest_name_length": 7}
{"curie": "MONDO:0016083", "names": ["FLOTCH syndrome", "Friedel Heid Grosshans syndrome", "leukonychia totalis-trichilemmal cysts-ciliary dystrophy syndrome", "Leukonychia totalis-trichilemmal cysts-ciliary dystrophy syndrome", "Leukonychia totalis, trichilemmal cysts, ciliary dystrophy syndrome", "Leukonychia totalis, trichilemmal cysts, ciliary dystrophy syndrome (disorder)", "familial occurrence of total leukonychia, trichilemmal cysts and ciliary dystrophy with dominant autosomal heredity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FLOTCH syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0010533", "names": ["ARTS", "Arts", "MRXS18", "MRXSARTS", "ARTS SYNDROME", "Arts syndrome", "Arts syndrome, X-linked recessive", "Lethal ataxia-deafness-optic atrophy", "lethal ataxia-deafness-optic atrophy", "Ataxia-Deafness-Optic Atrophy, Lethal", "syndromic X-linked mental retardation 18", "mental retardation, X-linked, syndromic 18", "MENTAL RETARDATION, X-LINKED, SYNDROMIC 18", "syndromic X-linked intellectual disability 18", "lethal ataxia with deafness and optic atrophy", "Lethal ataxia with deafness and optic atrophy", "syndromic X-linked mental retardation Arts type", "intellectual disability, X-linked, syndromic 18", "Lethal ataxia with hearing loss and optic atrophy", "mental retardation, X-linked, syndromic, Arts type", "MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARTS TYPE", "syndromic X-linked intellectual disability Arts type", "Fatal X-linked ataxia with deafness and loss of vision", "fatal X-linked ataxia with deafness and loss of vision", "X-linked fatal ataxia with deafness and loss of vision", "intellectual disability, X-linked, syndromic, Arts type", "ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION", "Ataxia, Fatal X-Linked, with Deafness and Loss of Vision", "ataxia, fatal X-linked, with deafness and loss of vision", "Fatal X-linked ataxia with deafness and loss of vision (disorder)", "Fatal X-linked ataxia with deafness and loss of vision (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arts syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0003888", "names": ["Childhood Teratocarcinoma of Testis", "childhood teratocarcinoma of testis", "Pediatric Testicular Teratocarcinoma", "childhood testicular teratocarcinoma", "pediatric testicular Teratocarcinoma", "Childhood Testicular Teratocarcinoma", "pediatric testicular teratocarcinoma", "childhood teratocarcinoma of the testis", "Childhood Teratocarcinoma of the Testis", "Childhood Testicular Mixed Embryonal Carcinoma and Teratoma", "childhood testicular mixed embryonal carcinoma and teratoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood testicular mixed embryonal carcinoma and teratoma", "shortest_name_length": 35}
{"curie": "MONDO:0005451", "names": ["Eating disorder", "eating disorder", "Eating Disorder", "EATING DISORDER", "Disorder, Eating", "eating disorders", "disorder; eating", "EATING DISORDERS", "Eating disorders", "eating; disorder", "Eating Disorders", "Disorders, Eating", "Eating disorder NOS", "EATING DISORDER NOS", "Eating disorder, NOS", "Eating disorder (disorder)", "eating disorder (diagnosis)", "feeding and eating disorder", "Eating and Feeding Disorders", "Feeding and Eating Disorders", "Feeding and eating disorders", "Eating disorder, unspecified", "Eating disorders and disturbances"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eating disorder", "shortest_name_length": 15}
{"curie": "UMLS:C0235884", "names": ["Gastric Perforation", "gastric perforation", "GASTRIC PERFORATION", "Gastric perforation", "Perforation stomach", "Stomach perforation", "PERFORATION STOMACH", "stomach perforation", "STOMACH PERFORATION", "perforation stomach", "stomach; perforation", "STOMACH, PERFORATION", "Perforation of stomach", "gastric perforation (diagnosis)", "Perforation of stomach (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perforation of stomach", "shortest_name_length": 19}
{"curie": "UMLS:C4288302", "names": ["Refractory Acute Lymphoblastic Leukemia (ALL)", "Refractory Adult Acute Lymphoblastic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Adult Acute Lymphoblastic Leukemia", "shortest_name_length": 45}
{"curie": "MONDO:0002202", "names": ["outlet dysfunction constipation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "outlet dysfunction constipation", "shortest_name_length": 31}
{"curie": "UMLS:C4683632", "names": ["St. Jude Stage IV Childhood Non-Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "St. Jude Stage IV Childhood Non-Hodgkin Lymphoma AJCC v8", "shortest_name_length": 56}
{"curie": "UMLS:C2828015", "names": ["Stage IIC Merkel Cell Carcinoma", "Stage IIC Merkel Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIC Merkel Cell Carcinoma AJCC v7", "shortest_name_length": 31}
{"curie": "UMLS:C5420538", "names": ["Unresectable Salivary Gland Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Salivary Gland Carcinoma", "shortest_name_length": 37}
{"curie": "UMLS:C4744707", "names": ["Colon Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colon Liposarcoma", "shortest_name_length": 17}
{"curie": "UMLS:C0848859", "names": ["ear carcinoma", "Ear Carcinoma", "carcinoma ear", "Ear carcinoma", "Carcinoma;ear", "carcinoma of the ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ear carcinoma", "shortest_name_length": 13}
{"curie": "UMLS:C0949083", "names": ["Nosocomial pneumonia", "nosocomial pneumonia", "Nosocomial Pneumonia", "pneumonia nosocomial", "nosocomial pneumonias", "hospital acquired pneumonia", "Hospital acquired pneumonia", "hospital-acquired pneumonia", "Hospital Acquired Pneumonia", "PNEUMONIA HOSPITAL ACQUIRED", "pneumonia hospital acquired", "Hospital Acquired Pneumonias", "acquired hospital pneumonias", "Pneumonia, Hospital Acquired", "Nosocomial pneumonia (disorder)", "HAP - hospital acquired pneumonia", "hospital-acquired pneumonia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hospital acquired pneumonia", "shortest_name_length": 20}
{"curie": "UMLS:C1336808", "names": ["Transplant-Related Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transplant-Related Carcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0007895", "names": ["PLSDT", "PLSDL", "PLSD-T", "thanatophoric dysplasia, Luton variant", "THANATOPHORIC DYSPLASIA, LUTON VARIANT", "Torrance type platyspondylic dysplasia", "Platyspondylic dysplasia, Torrance type", "platyspondylic dysplasia, Torrance type", "thanatophoric dysplasia Torrance variant", "thanatophoric dysplasia, Torrance variant", "Thanatophoric Dysplasia, Torrance Variant", "THANATOPHORIC DYSPLASIA, TORRANCE VARIANT", "Platyspondylic dysplasia, Torrance-Luton type", "platyspondylic dysplasia, Torrance-Luton type", "Platyspondylic Skeletal Dysplasia, Torrance Type", "PLATYSPONDYLIC SKELETAL DYSPLASIA, TORRANCE TYPE", "platyspondylic skeletal dysplasia, Torrance type", "PLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, LUTON TYPE", "Platyspondylic lethal skeletal dysplasia, Luton type", "Platyspondylic lethal skeletal dysplasia Torrance type", "Platyspondylic Lethal Skeletal Dysplasia, Torrance Type", "PLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, TORRANCE TYPE", "Platyspondylic lethal skeletal dysplasia, Torrance type", "platyspondylic lethal skeletal dysplasia, Torrance type", "lethal short-limbed Platyspondylic dwarfism Torrance type", "lethal short-limbed platyspondylic dwarfism, Torrance type", "LETHAL SHORT-LIMBED PLATYSPONDYLIC DWARFISM, TORRANCE TYPE", "lethal short-limbed Platyspondylic dwarfism, Torrance type", "Lethal Short-Limbed Platyspondylic Dwarfism, Torrance Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "platyspondylic dysplasia, Torrance type", "shortest_name_length": 5}
{"curie": "UMLS:C1708864", "names": ["Malignant Central Nervous System Germ Cell Tumor", "Malignant Central Nervous System Germ Cell Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Central Nervous System Germ Cell Tumor", "shortest_name_length": 48}
{"curie": "UMLS:C0521845", "names": ["Drug effect decreased", "Drug action decreased", "Drug effect diminished", "DRUG EFFECT DEMINISHED", "Drug action decreased (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drug action decreased", "shortest_name_length": 21}
{"curie": "UMLS:C5418913", "names": ["Unresectable Fallopian Tube Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Fallopian Tube Adenocarcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0006881", "names": ["cellulitis; orbit", "orbit; cellulitis", "cellulitis orbital", "orbital cellulitis", "Orbital Cellulitis", "Cellulitis orbital", "Orbital cellulitis", "Cellulitis of orbit", "Cellulitis, Orbital", "CELLULITIS, ORBITAL", "Orbital Cellulitides", "Cellulitides, Orbital", "Orbital cellulitis (disorder)", "Postseptal orbital cellulitis", "orbital cellulitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orbital cellulitis", "shortest_name_length": 17}
{"curie": "MONDO:0008305", "names": ["Scra1", "SCRA1", "Currarino triad", "CURRARINO TRIAD", "CURRARINO syndrome", "Currarino syndrome", "CURRARINO SYNDROME", "sacral agenesis syndrome", "Currarino triad (disorder)", "partial sacral agenesis with intact first sacral vertebra, presacral mass and anorectal malformation", "Sacral Agenesis, Hereditary, With Presacral Mass, Anterior Meningocele, And-Or Teratoma, And Anorectal Malformation", "SACRAL AGENESIS, HEREDITARY, WITH PRESACRAL MASS, ANTERIOR MENINGOCELE, AND/OR TERATOMA, AND ANORECTAL MALFORMATION", "sacral agenesis, hereditary, with presacral Mass, anterior meningocele, and/or teratoma, and anorectal malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Currarino triad", "shortest_name_length": 5}
{"curie": "UMLS:C3829183", "names": ["Stage IVb", "Masaoka Stage IVb", "Masaoka-Koga Stage IVb"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Masaoka-Koga Stage IVb", "shortest_name_length": 9}
{"curie": "MONDO:0019825", "names": ["congenital coronary aneurysm", "Congenital coronary aneurysm", "coronary; aneurysm, congenital", "congenital; aneurysm, coronary", "aneurysm; coronary, congenital", "aneurysm; congenital, coronary", "Congenital coronary artery aneurysm", "congenital coronary artery aneurysm", "Congenital coronary (artery) aneurysm", "Congenital coronary aneurysm (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital coronary artery aneurysm", "shortest_name_length": 28}
{"curie": "MONDO:0001462", "names": ["Ca descending colon", "descending colon cancer", "Descending colon cancer", "cancer of descending colon", "Cancer of descending colon", "Malignant neoplasm of left colon", "malignant neoplasm of left colon", "malignant descending colon neoplasm", "malignant tumor of descending colon", "Malignant tumor of descending colon", "Malignant tumour of descending colon", "Malignant neoplasm of descending colon", "malignant neoplasm of descending colon", "Malignant tumor of descending colon (disorder)", "malignant neoplasm of descending colon (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "descending colon cancer", "shortest_name_length": 19}
{"curie": "MONDO:0006266", "names": ["Leydig cell tumor", "Leydig Cell Tumor", "LEYDIG CELL TUMOR", "leydig cell tumor", "leydig cell tumour", "cells leydig tumor", "Leydig cell tumour", "Leydig cell tumors", "cell leydig tumors", "cell leydig tumour", "Tumor, Leydig Cell", "leydig cell neoplasm", "Leydig cell neoplasm", "Leydig Cell Neoplasm", "Leydig cell tumor NOS", "Leydig cell neoplasia", "Leydig cell tumour NOS", "Leydig cell tumor, NOS", "Leydig cell tumour, NOS", "Interstitial cell tumor", "Interstitial Cell Tumor", "interstitial cell tumor", "Tumor, Interstitial Cell", "Interstitial cell tumour", "Interstitial Cell Tumors", "Tumors, Interstitial Cell", "Interstitial Cell Neoplasm", "interstitial cell neoplasm", "Interstitial cell tumor, NOS", "Interstitial cell tumour, NOS", "TESTIS, INTERSTITIAL CELL TUMOR", "Leydig cell tumor, undetermined"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leydig cell tumor", "shortest_name_length": 17}
{"curie": "MONDO:0021440", "names": ["Benign Skin Tumor", "benign skin tumor", "benign skin tumors", "Benign Tumor of Skin", "benign tumor of skin", "Neoplasm benign;skin", "benign skin neoplasm", "SKIN BENIGN NEOPLASM", "Benign Skin Neoplasm", "Skin benign neoplasm", "BENIGN SKIN NEOPLASM", "Benign tumor of skin", "Benign tumour of skin", "benign of skin tumors", "Skin neoplasms benign", "benign cutaneous tumor", "Skin Neoplasms, Benign", "skin neoplasms, benign", "Benign Cutaneous Tumor", "Benign Neoplasm of Skin", "benign neoplasm of skin", "Benign neoplasm of skin", "Benign skin neoplasm NOS", "Benign Tumor of the Skin", "benign tumor of the skin", "benign cutaneous neoplasm", "Benign Cutaneous Neoplasm", "Cutaneous neoplasms benign", "Benign Neoplasm of the Skin", "benign neoplasm of the skin", "zone of skin benign neoplasm", "Benign neoplasm of skin, NOS", "Benign neoplasm of skin (disorder)", "benign neoplasm of skin (diagnosis)", "Benign neoplasm of skin, site unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of skin", "shortest_name_length": 17}
{"curie": "UMLS:C4527332", "names": ["Recurrent Breast Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Breast Lymphoma", "shortest_name_length": 25}
{"curie": "UMLS:C4330495", "names": ["Intracranial Fibrous Histiocytoma", "Intracranial Benign Fibrous Histiocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intracranial Fibrous Histiocytoma", "shortest_name_length": 33}
{"curie": "MONDO:0032897", "names": ["IDDHBA", "intellectual developmental disorder with hypotonia and behavioral abnormalities", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPOTONIA AND BEHAVIORAL ABNORMALITIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder with hypotonia and behavioral abnormalities", "shortest_name_length": 6}
{"curie": "MONDO:0005993", "names": ["Human Trichomoniases", "Human Trichomoniasis", "Trichomonal Vaginitis", "TRICHOMONAS VAGINALIS", "VAGINITIS TRICHOMONAS", "trichomonas vaginitis", "Trichomoniases, Human", "Trichomonas vaginitis", "vaginitis trichomonas", "VAGINITIS TRICHOMONAL", "Vaginitis;trichomonal", "Vaginitis trichomonal", "Trichomonal vaginitis", "Trichomonas Vaginitis", "trichomonal vaginitis", "Trichomoniasis, Human", "trichomoniasis vaginal", "vaginal trichomoniasis", "Urogenital trichomonas", "urogenital Trichomonas", "Vaginitis, Trichomonas", "Trichomonal leukorrhea", "Vaginal trichomoniasis", "urogenital trichomonas", "Trichomoniasis, vaginal", "Trichomonal leukorrhoea", "Trichomonas Vaginitides", "Vaginitides, Trichomonas", "Trichomoniasis Urogenital", "urogenital trichomoniasis", "Urogenital trichomoniasis", "Trichomoniasis, urogenital", "Trichomonal vulvovaginitis", "Trichomonal fluor vaginalis", "trichomonas vaginalis vaginitis", "Trichomonal vaginitis (disorder)", "Trichomonal leukorrhea vaginalis", "Trichomonal vaginitis (diagnosis)", "Trichomonal leukorrhoea vaginalis", "Leukorrhea vaginalis - trichomonal", "Leukorrhoea vaginalis - trichomonal", "Trichomonas vaginalis trichomoniasis", "TV - Trichomonas vaginalis infection", "urogenital trichomoniasis (diagnosis)", "Urogenital trichomoniasis, unspecified", "TRICHOMONAS VAGINALIS INFECTION, FEMALE", "Trichs - Trichomonas vaginalis infection", "Trichomonas vaginitis urogenital infection", "urogenital infection by Trichomonas vaginalis", "Urogenital infection by Trichomonas vaginalis", "Urogenital infection caused by Trichomonas vaginalis", "urogenital infection caused by Trichomonas vaginalis", "Trichomonas vaginalis disease of genitourinary system", "Trichomonas vaginalis caused disease of genitourinary system", "Urogenital infection caused by Trichomonas vaginalis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Trichomonas vaginitis urogenital infection", "shortest_name_length": 20}
{"curie": "MONDO:0016262", "names": ["leiomyosarcoma uterus", "uterus leiomyosarcoma", "Uterine leiomyosarcoma", "UTERUS, LEIOMYOSARCOMA", "leiomyosarcoma uterine", "uterine leiomyosarcoma", "leiomyosarcoma - uterus", "leiomyosarcomas uterine", "Leiomyosarcoma - uterus", "leiomyosarcoma, uterine", "Leiomyosarcoma of Uterus", "Leiomyosarcoma of uterus", "leiomyosarcoma of uterus", "Corpus Uteri Leiomyosarcoma", "Uterine Body Leiomyosarcoma", "corpus uteri leiomyosarcoma", "uterine body leiomyosarcoma", "leiomyosarcoma of the uterus", "Leiomyosarcoma of the uterus", "Leiomyosarcoma of the Uterus", "Body of Uterus Leiomyosarcoma", "uterine corpus leiomyosarcoma", "body of uterus leiomyosarcoma", "Uterine Corpus Leiomyosarcoma", "Leiomyosarcoma of Corpus Uteri", "leiomyosarcoma of Corpus Uteri", "leiomyosarcoma of corpus uteri", "leiomyosarcoma of uterine body", "Leiomyosarcoma of corpus uteri", "Leiomyosarcoma of Uterine Body", "leiomyosarcoma of uterine corpus", "Leiomyosarcoma of Body of Uterus", "Leiomyosarcoma of Uterine Corpus", "leiomyosarcoma of body of uterus", "Leiomyosarcoma of body of uterus", "Leiomyosarcoma of the Uterine Body", "leiomyosarcoma of the uterine body", "Leiomyosarcoma of the corpus uteri", "leiomyosarcoma of the corpus uteri", "Leiomyosarcoma of the Corpus Uteri", "Leiomyosarcoma of uterus (disorder)", "leiomyosarcoma of uterus (diagnosis)", "Leiomyosarcoma of the Body of Uterus", "leiomyosarcoma of the uterine corpus", "leiomyosarcoma of the body of uterus", "Leiomyosarcoma of the Uterine Corpus", "Leiomyosarcoma of corpus uteri (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leiomyosarcoma of the corpus uteri", "shortest_name_length": 21}
{"curie": "MONDO:0002299", "names": ["glomangioma", "Glomangioma", "Glomangiomas", "glomangiomas", "Glomuvenous Malformation", "Glomangioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glomangioma", "shortest_name_length": 11}
{"curie": "MONDO:0013900", "names": ["AHC2", "ALTERNATING HEMIPLEGIA OF CHILDHOOD 2", "alternating hemiplegia of childhood 2", "alternating hemiplegia of childhood type 2", "ATP1A3 alternating hemiplegia of childhood", "alternating hemiplegia of childhood caused by mutation in ATP1A3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alternating hemiplegia of childhood 2", "shortest_name_length": 4}
{"curie": "UMLS:C0432261", "names": ["Osteopetrosis - intermediate type", "Osteopetrosis - intermediate type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Osteopetrosis - intermediate type", "shortest_name_length": 33}
{"curie": "UMLS:C0274862", "names": ["Organic arsenic poisoning", "Organic Arsenic Poisoning", "Poisoning, Organic Arsenic", "Organic Arsenic Poisonings", "Arsenic Poisoning, Organic", "Poisonings, Organic Arsenic", "Arsenic Poisonings, Organic", "Organic arsenic poisoning (disorder)", "Nervous System, Organic Arsenic Poisoning", "Organic Arsenic Poisoning, Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nervous System, Organic Arsenic Poisoning", "shortest_name_length": 25}
{"curie": "UMLS:C4744373", "names": ["Sellar Neurinoma", "Sellar Schwannoma", "Sellar Neurilemmoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sellar Schwannoma", "shortest_name_length": 16}
{"curie": "MONDO:0015974", "names": ["SCID", "scid", "scids", "SCID, NOS", "combined immunodeficiency severe", "severe combined immunodeficiency", "Severe Combined Immunodeficiency", "Severe combined immunodeficiency", "IMMUNODEFICIENCY, SEVERE COMBINED", "Immunodeficiency, severe combined", "Combined Immunodeficiency, Severe", "Severe Combined Immune Deficiency", "Immunodeficiency, Severe Combined", "combined immunodeficiencies severe", "Severe Combined Immunodeficiencies", "Combined Immunodeficiencies, Severe", "Immunodeficiencies, Severe Combined", "Severe Combined Immunologic Deficiency", "Immunologic Deficiency, Severe Combined", "Severe combined immunodeficiency (SCID)", "SCID - Severe combined immunodeficiency", "severe combined immunodeficiency disease", "Severe combined immunodeficiency disease", "Severe Combined Immunodeficiency Syndrome", "combined; immunodeficiency, severe (SCID)", "Severe combined immunodeficiency syndrome", "immunodeficiency; combined, severe (SCID)", "Immunodeficiency Syndrome, Severe Combined", "severe combined immunodeficiency (disease)", "Combined T-cell and B-cell immunodeficiency", "Severe combined immunodeficiency disease, NOS", "combined T and B cell inborn immunodeficiency", "Severe combined immunodeficiency disease (disorder)", "severe combined immunodeficiency disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe combined immunodeficiency", "shortest_name_length": 4}
{"curie": "UMLS:C0852343", "names": ["Polycythaemia (excl rubra vera)", "Polycythemia (excluding rubra vera)", "Polycythemia (Excluding Rubra Vera)", "Polycythemia (Excluding Polycythemia Vera)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Polycythaemia (excl rubra vera)", "shortest_name_length": 31}
{"curie": "UMLS:C0678236", "names": ["disease rare", "Rare Disease", "rare disease", "Rare diseases", "rare diseases", "Rare Diseases", "diseases rare", "Rare Disorder", "Disease, Rare"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rare Diseases", "shortest_name_length": 12}
{"curie": "UMLS:C0549334", "names": ["PAROTID DUCT OBSTRUCTION", "Parotid duct obstruction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parotid duct obstruction", "shortest_name_length": 24}
{"curie": "MONDO:0017054", "names": ["thiamine-responsive MSUD", "thiamine-responsive BCKD deficiency", "thiamine-responsive maple syrup urine disease", "thiamine-responsive branched-chain 2-ketoacid dehydrogenase deficiency", "thiamine-responsive branched-chain alpha-ketoacid dehydrogenase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thiamine-responsive maple syrup urine disease", "shortest_name_length": 24}
{"curie": "UMLS:C0024306", "names": ["Pleomorphic Lymphoma", "Lymphoma, Pleomorphic", "Pleomorphic Lymphomas", "Undifferentiated Lymphoma", "Lymphoma, Undifferentiated", "Undifferentiated Lymphomas", "undifferentiated cell; lymphoma", "lymphoma; undifferentiated cell", "Diffuse non-Hodgkin lymphoma, undifferentiated", "Diffuse non-Hodgkin's lymphoma, undifferentiated", "Undifferentiated (diffuse) non-Hodgkin's lymphoma", "Diffuse non-Hodgkin's lymphoma, undifferentiated (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoma, Undifferentiated", "shortest_name_length": 20}
{"curie": "MONDO:0009419", "names": ["WDSKS", "Woodhouse Sakati syndrome", "woodhouse-Sakati syndrome", "Woodhouse-Sakati Syndrome", "woodhouse Sakati syndrome", "WOODHOUSE-SAKATI SYNDROME", "Woodhouse-Sakati syndrome", "Diabetes-hypogonadism-deafness-intellectual disability syndrome", "diabetes-hypogonadism-deafness-intellectual disability syndrome", "Diabetes, hypogonadism, deafness, intellectual disability syndrome", "diabetes, hypogonadism, deafness, intellectual disability syndrome", "diabetes-hypogonadism-hearing loss-intellectual disability syndrome", "Diabetes-hypogonadism-hearing loss-intellectual disability syndrome", "Diabetes, hypogonadism, deafness, intellectual disability syndrome (disorder)", "diabetes, hypogonadism, deafness, intellectual disability syndrome (diagnosis)", "Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, and Extrapyramidal Syndrome", "progressive extrapyramidal disorder with primary hypogonadism, mental retardation, alopecia", "Extrapyramidal Disorder, Progressive, With Primary Hypogonadism, Mental Retardation, and Alopecia", "extrapyramidal disorder, progressive, with primary hypogonadism, mental retardation, and alopecia", "EXTRAPYRAMIDAL DISORDER, PROGRESSIVE, WITH PRIMARY HYPOGONADISM, MENTAL RETARDATION, AND ALOPECIA", "hypogonadism, alopecia, diabetes mellitus, mental retardation, deafness, and extrapyramidal syndrome", "Hypogonadism, diabetes mellitus, alopecia ,mental retardation and electrocardiographic abnormalities", "HYPOGONADISM, ALOPECIA, DIABETES MELLITUS, MENTAL RETARDATION, DEAFNESS, AND EXTRAPYRAMIDAL SYNDROME", "hypogonadism, diabetes mellitus, alopecia, mental retardation, and electrocardiographic abnormalities", "extrapyramidal disorder, progressive, with primary hypogonadism, intellectual disability, and alopecia", "hypogonadism, alopecia, diabetes mellitus, intellectual disability, deafness, and extrapyramidal syndrome", "hypogonadism, diabetes mellitus, alopecia, intellectual disability, and electrocardiographic abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Woodhouse-Sakati syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C4744470", "names": ["Medullary Hemangioblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Medullary Hemangioblastoma", "shortest_name_length": 26}
{"curie": "UMLS:C1335019", "names": ["Non-Neoplastic Lung Disorder", "Non-neoplastic Lung Disorders", "Non-neoplastic Pulmonary Disease", "Non-neoplastic Pulmonary Diseases", "Non-Neoplastic Pulmonary Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Lung Disorder", "shortest_name_length": 28}
{"curie": "MONDO:0018765", "names": ["CMUSE", "cryptogenic multifocal ulcerous stenosing enteritis", "Cryptogenic multifocal ulcerous stenosing enteritis", "Cryptogenic multifocal ulcerous stenosing enteritis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cryptogenic multifocal ulcerous stenosing enteritis", "shortest_name_length": 5}
{"curie": "MONDO:0013468", "names": ["RP59", "CDG1BB", "retinitis pigmentosa 59", "RETINITIS PIGMENTOSA 59", "DHDDS retinitis pigmentosa", "retinitis pigmentosa type 59", "congenital disorder of glycosylation, type Ibb", "congenital disorder of glycosylation, type 1bb", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ibb", "retinitis pigmentosa caused by mutation in DHDDS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 59", "shortest_name_length": 4}
{"curie": "MONDO:0010585", "names": ["ED1", "HED", "EDA", "Eda1", "XHED", "EDA1", "HED1", "Xlhed", "XLHED", "ECTD1", "CST SYNDROME", "CST Syndrome", "CST syndrome", "Syndrome, CST", "CST Syndromes", "Syndromes, CST", "ectodermal dysplasia 1", "Ectodermal Dysplasia 1", "ECTODERMAL DYSPLASIA 1", "Ectodermal Dysplasia 1s", "Dysplasia 1, Ectodermal", "anhidrotic dysplasia ectodermal", "Anhidrotic ectodermal dysplasia", "anhidrotic ectodermal dysplasia", "Christ-Siemens-Touraine syndrome", "Christ Siemens Touraine Syndrome", "CHRIST-SIEMENS-TOURAINE SYNDROME", "christ-siemens-touraine syndrome", "Christ-Siemens-Touraine Syndrome", "Anhidrotic Ectodermal Dysplasia 1", "Hypohidrotic Ectodermal Dysplasia", "Hypohidrotic ectodermal dysplasia", "Ectodermal Dysplasia 1, Anhydrotic", "ectodermal dysplasia 1, anhidrotic", "Ectodermal Dysplasia 1, Anhidrotic", "ectodermal dysplasia, hypohidrotic, 1", "ECTODERMAL DYSPLASIA, HYPOHIDROTIC, 1", "CST - Christ-Siemens-Touraine syndrome", "X-linked anhidrotic ectodermal dysplasia", "anhidrotic ectodermal dysplasia X-linked", "Anhydrotic Ectodermal Dysplasia, X Linked", "Anhidrotic Ectodermal Dysplasia, X-Linked", "Anhydrotic Ectodermal Dysplasia, X-Linked", "Anhidrotic Ectodermal Dysplasia, X Linked", "X-linked hypohidrotic ectodermal dysplasia", "X-Linked Hypohydridic Ectodermal Dysplasia", "ECTODERMAL DYSPLASIA, ANHIDROTIC, X-LINKED", "Hypohidrotic ectodermal dysplasia syndrome", "hypohidrotic X-linked ectodermal dysplasia", "hypohidrotic ectodermal dysplasia X-linked", "Hypohidrotic X-linked ectodermal dysplasia", "X Linked Hypohydridic Ectodermal Dysplasia", "Ectodermal Dysplasia, Anhidrotic, X-Linked", "ectodermal dysplasia, anhidrotic, X-linked", "hypohidrotic ectodermal dysplasia, X-linked", "hypohidrotic ectodermal dysplasia, X-Linked", "Ectodermal Dysplasia, Hypohidrotic, X-Linked", "Ectodermal Dysplasia, Hypohydridic, X-Linked", "ectodermal dysplasia 1, hypohidrotic, X-linked", "ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED", "Hypohidrotic ectodermal dysplasia syndrome, NOS", "Anhidrotic ectodermal dysplasia syndrome, hereditary", "Hypohidrotic X-linked ectodermal dysplasia (disorder)", "hypohidrotic X-linked ectodermal dysplasia (diagnosis)", "ectodermal dysplasia 1, hypohidrotic/hair/tooth type, X-linked", "ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC/HAIR/TOOTH TYPE, X-LINKED", "ectodermal dysplasia 1, hypohidrotic/hair/Tooth type, X-linked", "ectodermal dysplasia 1, hypohidrotic, X-linked, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked hypohidrotic ectodermal dysplasia", "shortest_name_length": 3}
{"curie": "MONDO:0022859", "names": ["cor biloculare", "Cor Biloculare", "Cor biloculare", "cor; biloculare", "biloculare; cor", "TWO-chambered heart", "Cor biloculare (disorder)", "cor biloculare (diagnosis)", "Absence of atrial and ventricular septa", "Absence of atrial AND ventricular septa", "absence of atrial and ventricular septa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cor biloculare", "shortest_name_length": 14}
{"curie": "MONDO:0100081", "names": ["parasomnia", "sleep disorder", "Sleep Disorder", "Sleep disturbance", "sleep disturbance", "Sleep Dysfunction", "Sleep Disturbance", "sleep disturbances", "disturbances, sleep"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sleep disorder", "shortest_name_length": 10}
{"curie": "MONDO:0006424", "names": ["SOFTTISSUE", "Soft tissue tumor", "soft tissue tumor", "Soft Tissue Tumor", "SOFT TISSUE TUMOR", "Soft tissue tumors", "soft tissue tumors", "soft tissue tumour", "Soft tissue tumour", "Soft Tissue Tumors", "soft tissue tumours", "soft tissues tumors", "Tumor of Soft Tissue", "Soft tissue neoplasm", "soft tissue neoplasm", "tumor of soft tissue", "Soft Tissue Neoplasm", "soft tissues tumours", "of soft tissue tumor", "Tumor of soft tissue", "Soft Tissue Neoplasms", "Tumour of soft tissue", "Neoplasm, Soft Tissue", "Neoplasms, Soft Tissue", "Neoplasm of soft tissue", "Neoplasm of Soft Tissue", "neoplasm of soft tissue", "Tumor of the Soft Tissue", "Neoplasm of soft tissues", "tumor of the soft tissue", "Soft tissue neoplasm, NOS", "Neoplasm of the Soft Tissue", "neoplasm of the soft tissue", "Neoplasm of soft tissue (disorder)", "neoplasm of soft tissue (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "soft tissue neoplasm", "shortest_name_length": 10}
{"curie": "MONDO:0032912", "names": ["CSS11", "Coffin-Siris syndrome 11", "COFFIN-SIRIS SYNDROME 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Coffin-Siris syndrome 11", "shortest_name_length": 5}
{"curie": "MONDO:0012844", "names": ["CILD8", "primary ciliary dyskinesia 8", "Ciliary Dyskinesia, Primary, 8", "ciliary dyskinesia, primary, 8", "CILIARY DYSKINESIA, PRIMARY, 8", "primary ciliary dyskinesia type 8", "primary ciliary dyskinesia 8 with or without situs inversus", "ciliary dyskinesia, primary, 8, with or without situs inversus", "CILIARY DYSKINESIA, PRIMARY, 8, WITH OR WITHOUT SITUS INVERSUS", "Ciliary Dyskinesia, Primary, 8, With Or Without Situs Inversus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia 8", "shortest_name_length": 5}
{"curie": "MONDO:0008340", "names": ["PTOS1", "ptosis congenital", "Congenital ptosis", "congenital ptosis", "Congenital Ptosis", "ptosis; congenital", "ptosis, congenital", "Ptosis, congenital", "congenital; ptosis", "Congenital ptosis, NOS", "Congenital Eyelid Ptosis", "Eyelid ptosis congenital", "congenital eyelid ptosis", "Congenital Blepharoptosis", "blepharoptosis; congenital", "eyelid; ptosis, congenital", "congenital; blepharoptosis", "ptosis; eyelid, congenital", "congenital ptosis (disease)", "Congenital ptosis of eyelid", "Congenital ptosis (disorder)", "congenital ptosis (diagnosis)", "eyelid congenital upper ptosis", "Ptosis, Hereditary Congenital 1", "ptosis, hereditary congenital 1", "PTOSIS, HEREDITARY CONGENITAL 1", "Congenital drooping upper eyelid", "ptosis, hereditary congenital, 1", "Congenital ptosis of upper eyelid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ptosis, hereditary congenital, 1", "shortest_name_length": 5}
{"curie": "UMLS:C4727413", "names": ["Recurrent Parotid Gland Mucoepidermoid Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Parotid Gland Mucoepidermoid Carcinoma", "shortest_name_length": 48}
{"curie": "MONDO:0006803", "names": ["imi", "inferior mi", "Inferior MI", "mi inferior", "inferior myocardial infarction", "Inferior myocardial infarction", "Inferior Myocardial Infarction", "MYOCARDIAL INFARCTION INFERIOR", "Infarction, Inferior Myocardial", "Myocardial Infarction, Inferior", "Inferior Myocardial Infarctions", "Myocardial Infarctions, Inferior", "Infarctions, Inferior Myocardial", "Inferior Wall Myocardial Infarction", "Diaphragmatic Myocardial Infarction", "Infarction, Diaphragmatic Myocardial", "Myocardial Infarction, Diaphragmatic", "Diaphragmatic Myocardial Infarctions", "Myocardial Infarction, Inferior Wall", "Myocardial Infarctions, Diaphragmatic", "Infarctions, Diaphragmatic Myocardial", "MYOCARDIAL INFARCTION (INFERIOR WALL)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inferior myocardial infarction", "shortest_name_length": 3}
{"curie": "UMLS:C0151693", "names": ["Adrenal bleeding", "Hemorrhage adrenal", "adrenal hemorrhage", "ADRENAL HEMORRHAGE", "Adrenal hemorrhage", "Adrenal Hemorrhage", "HEMORRHAGE ADRENAL", "hemorrhage; adrenal", "Adrenal haemorrhage", "adrenal; hemorrhage", "Haemorrhage adrenal", "ADRENAL HAEMORRHAGE", "adrenal haemorrhage", "Adrenal hemorrhage (disorder)", "adrenal hemorrhage (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adrenal hemorrhage", "shortest_name_length": 16}
{"curie": "MONDO:0006944", "names": ["aminoaciduria", "AMINOACIDURIA", "Aminoaciduria", "aminoacidurias", "Hyperaminoaciduria", "Aminoaciduria, NOS", "Renal Aminoaciduria", "renal aminoaciduria", "Aminoaciduria, Renal", "Renal Aminoacidurias", "Aminoacidurias, Renal", "Aminoaciduria (disorder)", "Aminoaciduria (diagnosis)", "Elevated urine amino acids", "inborn renal aminoaciduria", "High urine amino acid levels", "Amino acid increased in urine", "Urine amino acid level increased", "Amino acid level in urine elevated", "renal tubular disorder aminoaciduria", "Abnormal urinary amino-acid findings", "Increased levels of animo acids in urine", "Amino acid concentration in urine above normal", "Amino acid concentration in urine above normal (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal aminoaciduria", "shortest_name_length": 13}
{"curie": "UMLS:C1333068", "names": ["CCMMT", "Clear Cell Myomelanocytic Tumor", "Clear-Cell Myomelanocytic Tumor", "Myomelanocytic Tumor, Clear-Cell", "Tumor, Clear-Cell Myomelanocytic", "Clear-Cell Myomelanocytic Tumors", "Clear Cell Myomelanocytic Tumors", "Tumors, Clear-Cell Myomelanocytic", "Myomelanocytic Tumors, Clear-Cell", "Clear Cell Myomelanocytic Tumor of the Falciform Ligament/Ligamentum Teres"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clear-Cell Myomelanocytic Tumors", "shortest_name_length": 5}
{"curie": "MONDO:0030981", "names": ["IMD79", "CD4 DEFICIENCY", "CD4 Deficiency", "IMMUNODEFICIENCY 79", "immunodeficiency 79"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 79", "shortest_name_length": 5}
{"curie": "MONDO:0000405", "names": ["anal canal cancer", "Anal canal cancer", "cancer of anal canal", "Cancer of anal canal", "Anal canal cancer NOS", "Malignant tumor of anal canal", "malignant anal canal neoplasm", "Malignant tumour of anal canal", "Anal canal neoplasms malignant", "malignant neoplasm of anal canal", "Malignant neoplasm of anal canal", "Malignant tumor of anal canal (disorder)", "malignant neoplasm of anal canal (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anal canal cancer", "shortest_name_length": 17}
{"curie": "UMLS:C0334486", "names": ["Stromal myosis", "stromal myosis", "stromal; myosis", "myosis; stromal", "Stromal myosis, NOS", "Stromal endometriosis", "stromal; endometriosis", "endometriosis; stromal", "Endometrial stromatosis", "stromatosis; endometrial", "Endolymphatic Stromal Myoses", "Endolymphatic Stromal Myosis", "endolymphatic stromal myosis", "Endolymphatic stromal myosis", "Myosis, Endolymphatic Stromal", "Myoses, Endolymphatic Stromal", "Stromal Myosis, Endolymphatic", "Stromal Myoses, Endolymphatic", "Low grade endometrial stromal sarcoma", "Low Grade Endometrial Stromal Sarcoma", "Endometrial stromal sarcoma, low grade", "Low Grade Endometrioid Stromal Sarcoma", "Endometrioid stromal sarcoma, low grade", "Sarcoma, Endometrial Stromal, Low-Grade", "Low grade endometrial stromal sarcoma (disorder)", "Endometrial stromal sarcoma, low grade (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Grade Endometrial Stromal Sarcoma", "shortest_name_length": 14}
{"curie": "UMLS:C0677728", "names": ["Indolent Non-Hodgkin Lymphoma", "Indolent Adult Non-Hodgkin Lymphoma", "indolent, adult non-Hodgkin lymphoma", "adult indolent non-Hodgkin's lymphoma", "Adult Indolent Non-Hodgkin's Lymphoma", "indolent adult non-Hodgkin's lymphoma", "Indolent Adult Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Indolent Adult Non-Hodgkin Lymphoma", "shortest_name_length": 29}
{"curie": "MONDO:0005516", "names": ["Osteodysplasia", "chondrodystrophy", "Skeletal dysplasia", "skeletal dysplasia", "Skeletal Dysplasia", "dysplasia skeletal", "dysplasias skeletal", "osteochondrodysplasia", "Osteochondrodysplasia", "Osteochondrodysplasias", "OTHER SKELETAL DYSPLASIAS", "Osteochondrodysplasia, NOS", "Congenital skeletal dysplasia", "congenital skeletal dysplasia", "Congenital Skeletal Dysplasia", "Abnormal skeletal development", "Cartilage Development disorder", "osteochondrodysplasia syndrome", "Osteochondrodysplasia syndrome", "cartilage development disorder", "Congenital anomaly of cartilage", "congenital anomaly of cartilage", "OSTEOCHONDRODYSPLASIA SYNDROMES", "osteochondrodysplasia (diagnosis)", "Osteochondrodysplasia, unspecified", "Congenital skeletal dysplasia (disorder)", "Osteochondrodysplasia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteochondrodysplasia", "shortest_name_length": 14}
{"curie": "UMLS:C2712871", "names": ["Gout attack"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gout attack", "shortest_name_length": 11}
{"curie": "MONDO:0012156", "names": ["CMS1B", "congenital myasthenic syndrome 1B", "congenital myasthenic syndrome type 1B", "Myasthenic Syndrome, Congenital, Fast-Channel", "congenital myasthenic syndrome 1B, fast-channel", "myasthenic syndrome, congenital, 1B, fast-channel", "MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL", "myasthenic syndrome, congenital, 1B, FAST-channel"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myasthenic syndrome, congenital, 1B, fast-channel", "shortest_name_length": 5}
{"curie": "MONDO:0018354", "names": ["PWS-like", "Prader-Willi-like syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prader-Willi-like syndrome", "shortest_name_length": 8}
{"curie": "MONDO:0044705", "names": ["Paranasal Sinus Epidermoid Carcinoma", "paranasal sinus epidermoid carcinoma", "Paranasal Sinus Squamous Cell Carcinoma", "Epidermoid Carcinoma of Paranasal Sinus", "epidermoid carcinoma of paranasal sinus", "paranasal sinus squamous cell carcinoma", "Squamous Cell Carcinoma of Paranasal Sinus", "squamous cell carcinoma of paranasal sinus", "Epidermoid Carcinoma of the Paranasal Sinus", "epidermoid carcinoma of the paranasal sinus", "Squamous cell carcinoma of the paranasal sinus", "squamous cell carcinoma of the paranasal sinus", "Squamous Cell Carcinoma of the Paranasal Sinus", "squamous cell carcinoma of the nasal cavity and sinuses", "squamous cell carcinoma of the nasal cavity and paranasal sinuses"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paranasal sinus squamous cell carcinoma", "shortest_name_length": 36}
{"curie": "UMLS:C4683749", "names": ["Stage IVA1 Mycosis Fungoides and Sezary Syndrome AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA1 Mycosis Fungoides and Sezary Syndrome AJCC v8", "shortest_name_length": 56}
{"curie": "MONDO:0011983", "names": ["AITD4", "AUTOIMMUNE THYROID DISEASE, SUSCEPTIBILITY TO, 4", "autoimmune thyroid disease, susceptibility to, 4", "autoimmune thyroid disease, susceptibility to, type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune thyroid disease, susceptibility to, 4", "shortest_name_length": 5}
{"curie": "UMLS:C0577690", "names": ["PROTEUS SEPSIS", "Proteus septicemia", "septicemia proteus", "Proteus septicaemia", "Proteus septicemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Proteus septicemia", "shortest_name_length": 14}
{"curie": "MONDO:0007322", "names": ["chondrodysplasia punctata, Mt type", "CHONDRODYSPLASIA PUNCTATA, MT TYPE", "Chondrodysplasia punctata, MT type", "chondrodysplasia punctata, tibia-metacarpal type", "Chondrodysplasia Punctata, Tibia-Metacarpal Type", "CHONDRODYSPLASIA PUNCTATA, TIBIA-METACARPAL TYPE", "Chondrodysplasia punctata, tibia-metacarpal type", "chondrodysplasia punctata, tibial-metacarpal type", "Chondrodysplasia punctata, tibial-metacarpal type", "Chondrodysplasia punctata, tibia-metacarpal type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chondrodysplasia punctata, tibial-metacarpal type", "shortest_name_length": 34}
{"curie": "MONDO:8000015", "names": ["TRS", "ETRS", "SRXY11", "Anorchia", "Vanishing testes", "Vanishing Testes", "Vanishing testis", "anorchia, familial", "ANORCHIA, FAMILIAL", "Gonadal Regression", "Anorchia, Familial", "Testicular regression", "Testicular Regression", "46,XY sex reversal 11", "46,XY SEX REVERSAL 11", "46, XY sex reversal 11", "vanishing testis syndrome", "Vanishing testis syndrome", "Vanishing testes syndrome", "vanishing testes syndrome", "Xy Gonadal Agenesis Syndrome", "xy gonadal agenesis syndrome", "XY Gonadal agenesis syndrome", "XY gonadal agenesis syndrome", "testicular regression syndrome", "XY gonadal dysgenesis syndrome", "Testicular regression syndrome", "TESTICULAR REGRESSION SYNDROME", "testicular regression, embryonic", "Testicular Regression, Embryonic", "TESTICULAR REGRESSION, EMBRYONIC", "Testicular regression - embryonic", "vanishing testis syndrome (diagnosis)", "XY GONADAL AGENESIS/DYSGENESIS SYNDROME", "Embryonic testicular regression syndrome", "embryonic testicular regression syndrome", "Testicular regression syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XY sex reversal 11", "shortest_name_length": 3}
{"curie": "MONDO:0010885", "names": ["ANGIOKERATOMA CORPORIS DIFFUSUM WITH ARTERIOVENOUS FISTULAS", "Angiokeratoma Corporis Diffusum with Arteriovenous Fistulas", "angiokeratoma corporis diffusum with arteriovenous fistulas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angiokeratoma corporis diffusum with arteriovenous fistulas", "shortest_name_length": 59}
{"curie": "UMLS:C2346458", "names": ["I", "Stage I Multiple Myeloma", "Multiple Myeloma Stage I", "Stage I Plasma Cell Myeloma", "ISS Stage I Multiple Myeloma", "ISS Stage I Plasma Cell Myeloma", "ISS Stage I Multiple Myeloma/Plasma Cell Myeloma", "International Staging System Stage I Multiple Myeloma", "International Staging System Stage I Plasma Cell Myeloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ISS Stage I Plasma Cell Myeloma", "shortest_name_length": 1}
{"curie": "MONDO:0024643", "names": ["myocardial disease", "myocardium disease", "Myocardial disorder", "Myocardial Disorder", "myocardial disorder", "Myocardial disorders", "Myocardial Disorders", "myocardial disorders", "disease of myocardium", "disorder of myocardium", "disorder of heart muscle", "myocardium disease or disorder", "myocardial disorders (diagnosis)", "disease or disorder of myocardium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myocardial disorder", "shortest_name_length": 18}
{"curie": "UMLS:C4688331", "names": ["BRCA-Mutated Ovarian Carcinoma", "BRCA-Associated Ovarian Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "BRCA-Associated Ovarian Carcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0018868", "names": ["mld", "MLD", "Scholz", "MLD, NOS", "MLD, juvenile form", "Sulfatide Lipidosis", "SULFATIDE LIPIDOSIS", "Sulfatide lipidosis", "Lipidosis, Sulfatide", "Sulphatide lipidosis", "sulfatide lipoidosis", "lipidosis; sulfatide", "sulfatide; lipidosis", "Sulfatide lipidosis, NOS", "Scholz cerebral sclerosis", "Arylsulfatase A deficiency", "arylsulfatase A deficiency", "van Bogaert-Nijssen disease", "metachromatic leukodystrophy", "Metachromatic Leukodystrophy", "leukodystrophy metachromatic", "Metachromatic leukoencephaly", "Metachromatic leucodystrophy", "METACHROMATIC LEUKODYSTROPHY", "Metachromatic leukodystrophy", "metachromatic leukoencephaly", "metachromatic leucodystrophy", "Leukodystrophy, Metachromatic", "Leukodystrophy, metachromatic", "Metachromatic Leukodystrophies", "Leukodystrophies, Metachromatic", "CEREBROSIDE SULFATASE DEFICIENCY", "Metachromatic leukodystrophy, NOS", "METACHROMATIC LEUKOENCEPHALOPATHY", "Metachromatic Leukoencephalopathy", "metachromatic leukoencephalopathy", "metachromatic; leukoencephalopathy", "Arylsulfatase A Deficiency Disease", "leukoencephalopathy; metachromatic", "Leukoencephalopathy, Metachromatic", "LEUKOENCEPHALOPATHY, METACHROMATIC", "MLD - Metachromatic leucodystrophy", "Metachromatic Leukoencephalopathies", "deficiency of cerebroside-sulfatase", "Leukoencephalopathies, Metachromatic", "Juvenile metachromatic leucodystrophy", "Juvenile Metachromatic Leukodystrophy", "brain; sclerosis, progressive familial", "sclerosis; brain, progressive familial", "Metachromatic Leukodystrophy, Juvenile", "METACHROMATIC LEUKODYSTROPHY, JUVENILE", "Leukodystrophy, Juvenile Metachromatic", "Leukodystrophy, Metachromatic, Juvenile", "Familial progressive cerebral sclerosis", "Metachromatic leucodystrophy (disorder)", "Juvenile Metachromatic Leukodystrophies", "Leukodystrophies, Juvenile Metachromatic", "metachromatic leukodystrophy (diagnosis)", "Metachromatic Leukodystrophies, Juvenile", "Arylsulfatase A deficiency, juvenile form", "Cerebroside Sulphatase Deficiency Disease", "Juvenile-Type Metachromatic Leukodystrophy", "Metachromatic Leukodystrophy, Juvenile-Type", "Leukodystrophy, Juvenile-Type Metachromatic", "Metachromatic Leukodystrophy, Juvenile Type", "Metachromatic leukodystrophy, juvenile form", "Metachromatic leucodystrophy, juvenile type", "Metachromatic leukodystrophy, juvenile type", "metachromatic leukodystrophy, juvenile type", "Juvenile-Type Metachromatic Leukodystrophies", "Metachromatic Leukodystrophies, Juvenile-Type", "Leukodystrophies, Juvenile-Type Metachromatic", "Cerebral sclerosis, Diffuse, Metachromatic Form", "CEREBRAL SCLEROSIS, DIFFUSE, METACHROMATIC FORM", "Metachromatic leukodystrophy, juvenile type (disorder)", "metachromatic leukodystrophy, juvenile type (diagnosis)", "Scholz-Bielschowsky-Henneberg diffuse cerebral sclerosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metachromatic leukodystrophy", "shortest_name_length": 3}
{"curie": "MONDO:0029141", "names": ["USH4", "Usher syndrome, type 4", "USHER SYNDROME, TYPE IV", "Usher syndrome, type IV"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Usher syndrome, type 4", "shortest_name_length": 4}
{"curie": "MONDO:0020681", "names": ["EDSMC", "EDSMC1", "Dundar syndrome", "Ehlers-Danlos syndrome, type Vib", "adducted thumb-clubfoot syndrome", "Ehlers-Danlos syndrome, type Vib, formerly", "Ehlers-Danlos syndrome musculocontractural type 1", "Ehlers-Danlos syndrome, musculocontractural type 1", "Ehlers-Danlos Syndrome, Musculocontractural Type 1", "Ehlers-Danlos syndrome, musculocontractural type, 1", "Arthrogryposis, Distal, with peculiar facies and hydronephrosis", "adducted thumb, clubfoot, and Progressive Joint and skin laxity syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ehlers-Danlos syndrome, musculocontractural type 1", "shortest_name_length": 5}
{"curie": "MONDO:0012400", "names": ["CDFES", "PTHSL1", "CDFE SYNDROME", "CDFE Syndrome", "CDFE syndrome", "Pitt-Hopkins-Like Syndrome 1", "PITT-HOPKINS-LIKE SYNDROME 1", "Pitt-Hopkins-like syndrome-1", "Pitt-Hopkins-like syndrome 1", "Pitt-Hopkins like syndrome 1", "cortical dysplasia-focal epilepsy syndrome", "Cortical Dysplasia-Focal Epilepsy Syndrome", "CORTICAL DYSPLASIA-FOCAL EPILEPSY SYNDROME", "Cortical dysplasia with focal epilepsy syndrome", "epilepsy localization-related cortical dysplasia", "CDFE (cortical dysplasia focal epilepsy) syndrome", "Cortical dysplasia with focal epilepsy syndrome (disorder)", "Cortical dysplasia with focal epilepsy syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cortical dysplasia-focal epilepsy syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C1334796", "names": ["Monoclonal Polymorphic Post-Transplant Lymphoproliferative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Monoclonal Polymorphic Post-Transplant Lymphoproliferative Disorder", "shortest_name_length": 67}
{"curie": "UMLS:C5205914", "names": ["Prostate Carcinoma Metastatic in the Pelvic Cavity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Carcinoma Metastatic in the Pelvic Cavity", "shortest_name_length": 50}
{"curie": "MONDO:0012990", "names": ["RP53", "LCA13", "RETINITIS PIGMENTOSA 53", "retinitis pigmentosa 53", "Leber congenital amaurosis 13", "LEBER CONGENITAL AMAUROSIS 13", "Leber Congenital Amaurosis 13", "RDH12 Leber congenital amaurosis", "Leber congenital amaurosis type 13", "Leber congenital amaurosis caused by mutation in RDH12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leber congenital amaurosis 13", "shortest_name_length": 4}
{"curie": "MONDO:0003644", "names": ["Colon Cavernous Angioma", "colon cavernous angioma", "Colonic Cavernous Angioma", "colonic cavernous angioma", "Cavernous Angioma of Colon", "Colon Cavernous Hemangioma", "colon cavernous hemangioma", "cavernous angioma of colon", "colonic cavernous hemangioma", "Colonic Cavernous Hemangioma", "Colonic Cavernous hemangioma", "cavernous hemangioma of colon", "Cavernous Hemangioma of Colon", "cavernous angioma of the colon", "Cavernous Angioma of the Colon", "Cavernous Hemangioma of the Colon", "cavernous hemangioma of the colon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cavernous hemangioma of colon", "shortest_name_length": 23}
{"curie": "MONDO:0013300", "names": ["Wide mouth", "Large mouth", "Macrostomia", "macrostomia", "Broad mouth", "Macrostomias", "Large oral aperture", "macrostomia, isolated", "MACROSTOMIA, ISOLATED", "Congenital macrostomia", "lateral cleft, isolated", "macrostomia (diagnosis)", "LATERAL CLEFT, ISOLATED", "commissural facial cleft", "transverse cleft, isolated", "TRANSVERSE CLEFT, ISOLATED", "COMMISSURAL CLEFT, ISOLATED", "commissural cleft, isolated", "macrostomia (physical finding)", "Congenital macrostomia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "commissural facial cleft", "shortest_name_length": 10}
{"curie": "MONDO:0019349", "names": ["Sotos", "SOTOS", "Nevo syndrome", "Soto Syndrome", "soto syndrome", "Cerebral giant", "Sotos Sequence", "Sotos sequence", "Sotos syndrome", "SOTOS SYNDROME", "sotos syndrome", "Sotos Syndrome", "Sotos' Syndrome", "Syndrome, Sotos", "Sequence, Sotos", "Sotos' syndrome", "sotos' syndrome", "Soto's Syndrome", "Giant, cerebral", "SOTOS1, FORMERLY", "Syndrome, Sotos'", "Cerebral Gigantism", "cerebral gigantism", "Cerebral gigantism", "CEREBRAL GIGANTISM", "Gigantism, Cerebral", "Cerebral Gigantisms", "Gigantisms, Cerebral", "SOTOS SYNDROME 1, FORMERLY", "Sotos' syndrome (disorder)", "Cerebral Gigantism Syndrome", "Sotos' syndrome (diagnosis)", "syndrome cerebral gigantism", "cerebral gigantism syndrome", "Cerebral gigantism syndrome", "CHROMOSOME 5q35 DELETION SYNDROME", "mental retardation-overgrowth sequence", "macrosomia-mental retardation syndrome", "distinctive facial appearance, overgrowth in childhood, and learning disabilities or delayed development"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sotos syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0003988", "names": ["Sternal Lymphoma", "sternal lymphoma", "sternum lymphoma", "lymphoma of sternum", "Lymphoma of Sternum", "Lymphoma of the Sternum", "lymphoma of the sternum", "primary sternal lymphoma", "Primary Sternal Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sternum lymphoma", "shortest_name_length": 16}
{"curie": "MONDO:0010204", "names": ["LAL Deficiency", "LAL deficiency", "Wolman disease", "lipa deficiency", "LIPA deficiency", "Acid lipase disease", "Acid lipase deficiency, NOS", "lysosomal and lipase deficiency", "Lysosomal acid lipase deficiency", "lysosomal acid lipase deficiency", "cholesteryl ester storage disease", "cholesterol ester hydrolase deficiency", "LAL (Lysosomal acid lipase) deficiency", "Cholesterol ester hydrolase deficiency", "LALD - Lysosomal acid lipase deficiency", "Lysosomal acid lipase deficiency (disorder)", "Acid cholesteryl ester hydrolase deficiency, type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lysosomal acid lipase deficiency", "shortest_name_length": 14}
{"curie": "MONDO:0002630", "names": ["SCOS", "Small cell osteosarcoma", "small cell osteosarcoma", "small cell Osteosarcoma", "round cell osteosarcoma", "Small Cell Osteosarcoma", "Round cell osteosarcoma", "osteosarcoma; small cell", "small cell; osteosarcoma", "small cell sarcoma of bone", "small cell osteogenic sarcoma", "Small Cell Osteogenic Sarcoma", "small cell sarcoma of bone (diagnosis)", "Small cell osteosarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small cell osteogenic sarcoma", "shortest_name_length": 4}
{"curie": "UMLS:C0850569", "names": ["rash allergic", "Allergic rash", "allergic rash", "Rash;allergic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Allergic rash", "shortest_name_length": 13}
{"curie": "UMLS:C0279726", "names": ["Pancreatic Delta Cell Adenoma", "pancreatic delta cell adenoma", "somatostatin secreting adenoma", "somatostatin producing adenoma", "adenoma, pancreatic delta cell", "adenoma, somatostatin producing", "pancreatic D islet cell adenoma", "adenoma, delta cell, pancreatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Delta Cell Adenoma", "shortest_name_length": 29}
{"curie": "UMLS:C0277550", "names": ["Endemic Disease", "Endemic disease", "endemic disease", "endemic diseases", "Disease, Endemic", "Endemic Disorder", "Endemic Diseases", "Diseases, Endemic", "Endemic disease, NOS", "Endemic disease (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endemic Diseases", "shortest_name_length": 15}
{"curie": "UMLS:C0847033", "names": ["Allergic edema", "edema allergic", "allergic edema", "Allergic oedema", "Oedema;allergic", "allergic oedema", "Allergic edema NOS", "Allergic oedema NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Allergic edema", "shortest_name_length": 14}
{"curie": "UMLS:C3831784", "names": ["AML M5", "Acute Myeloid Leukemia M5", "leukemia monocytic/monoblastic acute", "Acute monoblastic/monocytic leukemia", "Acute Monoblastic/Monocytic Leukemia", "Acute monocytic/monoblastic leukemia", "acute monoblastic/monocytic leukemia", "Acute monocytic/monoblastic leukaemia", "Acute monoblastic or monocytic leukemia", "Acute Monoblastic and Monocytic Leukemia", "Acute monoblastic and monocytic leukemia", "Acute monoblastic/monocytic leukemia NOS", "Acute monoblastic and monocytic leukaemia", "Acute monocytic/monoblastic leukemia (disorder)", "acute monoblastic/monocytic leukemia (diagnosis)", "Acute Monoblastic Leukemia and Acute Monocytic Leukemia", "Acute monoblastic and monocytic leukemia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute monocytic/monoblastic leukemia", "shortest_name_length": 6}
{"curie": "MONDO:0040753", "names": ["LTBI", "latent TB", "inactive TB", "latent tuberculosis", "Latent Tuberculosis", "Latent tuberculosis", "Latent Tuberculoses", "Tuberculosis, Latent", "Tuberculoses, Latent", "Inactive tuberculosis", "TUBERCULOSIS INACTIVE", "inactive tuberculosis", "Tuberculosis Infection", "latent tuberculosis infection", "Tuberculosis infection latent", "tuberculosis infection latent", "Latent Tuberculosis Infection", "Latent Tuberculosis Infections", "Infection, Latent Tuberculosis", "Tuberculosis Infection, Latent", "latent tuberculosis (diagnosis)", "Infections, Latent Tuberculosis", "Tuberculosis Infections, Latent", "Inactive tuberculosis (disorder)", "Latent tuberculosis infection (LTBI)", "LTBI - Latent tuberculosis infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "latent tuberculosis infection", "shortest_name_length": 4}
{"curie": "MONDO:0009904", "names": ["GTLMNS", "gitelman syndrome", "Gitelman syndrome", "GITELMAN SYNDROME", "Gitelman Syndrome", "gitelmans syndrome", "Syndrome, Gitelman", "gitelmans syndromes", "Gitelman's Syndrome", "Gitelman's syndrome", "Syndrome, Gitelman's", "Gitelman syndrome (disorder)", "Potassium and magnesium depletion", "POTASSIUM AND MAGNESIUM DEPLETION", "Potassium and Magnesium Depletion", "Familial hypokalemia-hypomagnesemia", "Familial Hypokalemia-Hypomagnesemia", "Familial Hypokalemia Hypomagnesemia", "familial hypokalemia-hypomagnesemia", "Hypokalemia-Hypomagnesemia, Familial", "Familial hypokalaemia-hypomagnesaemia", "Tubular Hypomagnesemia Hypokalemia with Hypocalcuria", "Tubular Hypomagnesemia-Hypokalemia with Hypocalcuria", "Primary Renotubular, Hypomagnesemia-Hypokalemia with Hypocalciuria", "Primary Renotubular, Hypokalemia-Hypomagnesemia with Hypocalciuria", "Hypokalemia-Hypomagnesemia, Primary Renotubular, with Hypocalciuria", "Hypomagnesemia-Hypokalemia, Primary Renotubular, with Hypocalciuria", "HYPOMAGNESEMIA-HYPOKALEMIA, PRIMARY RENOTUBULAR, WITH HYPOCALCIURIA", "hypomagnesemia-hypokalemia, primary renotubular, with hypocalciuria", "primary renal tubular hypokalemic hypomagnesemia with hypocalciuria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gitelman syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0008493", "names": ["OHS", "OHST", "STOMATOCYTOSIS I", "Stomatocytosis I", "stomatocytosis I", "stomatocytosis 1", "stomatocytosisIOHST", "Overhydrated hereditary stomatocytosis", "OVERHYDRATED hereditary stomatocytosis", "OVERHYDRATED HEREDITARY STOMATOCYTOSIS", "overhydrated hereditary stomatocytosis", "Overhydrated Hereditary Stomatocytosis", "potassium sodium disorder of erythrocyte", "Potassium-sodium disorder of erythrocyte", "Potassium-Sodium Disorder Of Erythrocyte", "POTASSIUM-SODIUM DISORDER OF ERYTHROCYTE", "Potassium sodium disorder of erythrocyte", "Overhydrated hereditary stomatocytosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "overhydrated hereditary stomatocytosis", "shortest_name_length": 3}
{"curie": "MONDO:0001179", "names": ["pinguicula", "Pinguicula", "pinguecula", "Pinguecula", "Pingueculas", "Pingueculum", "pingueculum", "Pinguecula (disorder)", "pinguecula (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pinguecula", "shortest_name_length": 10}
{"curie": "UMLS:C3494423", "names": ["Maxillary Retroposition", "Maxillary Retropositions", "Retroposition, Maxillary", "Retropositions, Maxillary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Maxillary Retroposition", "shortest_name_length": 23}
{"curie": "MONDO:0012054", "names": ["Sczd12", "SCZD12", "SCHIZOPHRENIA 12", "schizophrenia 12", "schizophrenia type 12", "SCHIZOPHRENIA SUSCEPTIBILITY LOCUS, CHROMOSOME 1p-RELATED", "schizophrenia susceptibility locus, chromosome 1P-related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schizophrenia 12", "shortest_name_length": 6}
{"curie": "UMLS:C1963718", "names": ["ORS", "Oculorespiratory syndrome", "Oculorespiratory Syndrome", "Oculo-Respiratory Syndrome", "Oculo-respiratory syndrome", "Oculo-respiratory-syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oculorespiratory syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C1708536", "names": ["Intermediate Grade Lung Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intermediate Grade Lung Neuroendocrine Neoplasm", "shortest_name_length": 47}
{"curie": "UMLS:C1336261", "names": ["Stage III Ovarian Embryonal Carcinoma", "Ovarian Embryonal Carcinoma, Stage III", "Stage III Ovarian Embryonal Carcinoma AJCC v7", "Stage III Ovarian Embryonal Carcinoma AJCC v6", "Stage III Ovarian Embryonal Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Ovarian Embryonal Carcinoma AJCC v6 and v7", "shortest_name_length": 37}
{"curie": "UMLS:C0854210", "names": ["Incomplete precocious puberty"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Incomplete precocious puberty", "shortest_name_length": 29}
{"curie": "MONDO:0013191", "names": ["FSGS5", "FOCAL SEGMENTAL GLOMERULOSCLEROSIS 5", "focal segmental glomerulosclerosis 5", "Focal Segmental Glomerulosclerosis 5", "glomerulosclerosis, focal segmental, 5", "GLOMERULOSCLEROSIS, FOCAL SEGMENTAL, 5", "INF2 focal segmental glomerulosclerosis", "focal segmental glomerulosclerosis type 5", "focal segmental glomerulosclerosis caused by mutation in INF2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal segmental glomerulosclerosis 5", "shortest_name_length": 5}
{"curie": "UMLS:C0334550", "names": ["Malignant chondroblastoma", "Chondroblastoma, malignant", "Metastasizing Chondroblastoma", "Chondroblastoma, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chondroblastoma, malignant", "shortest_name_length": 25}
{"curie": "MONDO:0006302", "names": ["MPSC", "SBT-MP", "micropapillary serous carcinoma", "Micropapillary Serous Carcinoma", "Micropapillary serous carcinoma", "Micropapillary Variant of Serous Borderline Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "micropapillary serous carcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0043777", "names": ["Rhinophyma", "rhinophyma", "Rhinophymas", "hypertrophic rosacea", "Hypertrophic rosacea", "Rhinophyma (disorder)", "rhinophyma (diagnosis)", "rhinophyma (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rhinophyma", "shortest_name_length": 10}
{"curie": "MONDO:0010212", "names": ["XP8", "XP4", "XPD", "XPH", "XP-D", "XPDC", "XP group D", "XP group H", "XP, Group H", "XP, GROUP D", "XP, Group D", "XPH, FORMERLY", "XP8, FORMERLY", "XP, Group H, formerly", "XP, GROUP H, FORMERLY", "xeroderma pigmentosum 4", "xeroderma pigmentosum IV", "XERODERMA PIGMENTOSUM IV", "Xeroderma Pigmentosum IV", "xeroderma pigmentosum VIII", "ERCC2 xeroderma pigmentosum", "xeroderma pigmentosum group D", "Xeroderma pigmentosum group D", "Xeroderma Pigmentosum Group D", "XP4 xeroderma pigmentosum VIII", "Xeroderma pigmentosum, group D", "xeroderma pigmentosum, group D", "xeroderma pigmentosum group type D", "XP4 XERODERMA PIGMENTOSUM VIII, FORMERLY", "XP4 xeroderma pigmentosum VIII, formerly", "Xeroderma pigmentosum, group D (disorder)", "XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D", "Xeroderma Pigmentosum, Complementation Group D", "xeroderma pigmentosum, complementation group D", "xeroderma pigmentosum caused by mutation in ERCC2", "xeroderma pigmentosum, complementation group type D"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "xeroderma pigmentosum group D", "shortest_name_length": 3}
{"curie": "MONDO:0009043", "names": ["GRTH", "Refetoff syndrome", "generalized resistance to thyroid hormone", "deafness-thyroid hormone resistance syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "generalized resistance to thyroid hormone", "shortest_name_length": 4}
{"curie": "UMLS:C4763750", "names": ["Platinum-Resistant Primary Peritoneal Cancer", "Platinum-Resistant Primary Peritoneal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Platinum-Resistant Primary Peritoneal Carcinoma", "shortest_name_length": 44}
{"curie": "UMLS:C4289798", "names": ["Childhood Infectious Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Infectious Disorder", "shortest_name_length": 29}
{"curie": "MONDO:0022736", "names": ["occupational lung disease", "Occupational lung disease", "LUNG DISEASE OCCUPATIONAL", "disease lung occupational", "lung disease occupational", "diseases lung occupational", "Occupational lung disorder", "diseases lungs occupational", "disorders lung occupational", "Occupational pulmonary disease", "Occupational lung disease, NOS", "Occupational inhalation disease", "Occupational lung disorder, NOS", "Occupational respiratory disease", "occupational respiratory disease", "Occupational pulmonary disease, NOS", "Occupational inhalation disease, NOS", "Occupational lung disease (disorder)", "Occupational respiratory disease, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "occupational lung disease", "shortest_name_length": 25}
{"curie": "UMLS:C0279921", "names": ["Childhood NSHD", "Pediatric NSHD", "NSHD, childhood", "NS HD, childhood", "pediatric HD, nodular sclerosis", "childhood HD, nodular sclerosis", "HD, nodular sclerosis, childhood", "nodular sclerosing HD, childhood", "Childhood Hodgkin's Nodular Sclerosis", "Pediatric Hodgkin's Nodular Sclerosis", "Childhood Nodular Sclerosis Hodgkin Lymphoma", "childhood nodular sclerosis Hodgkin lymphoma", "Nodular Sclerosis Classical Hodgkin Lymphoma", "pediatric Hogkin's disease, nodular sclerosis", "Childhood Nodular Sclerosis Hodgkin's Disease", "childhood nodular sclerosis Hodgkin's disease", "pediatric nodular sclerosis Hodgkin's disease", "Pediatric Nodular Sclerosis Hodgkin's Disease", "nodular sclerosis Hodgkin's disease, childhood", "childhood Hodgkin's disease, nodular sclerosis", "Pediatric Nodular Sclerosis Hodgkin's Lymphoma", "Childhood Nodular Sclerosis Hodgkin's Lymphoma", "Hodgkin's disease, nodular sclerosis, childhood", "nodular sclerosing Hodgkin's disease, childhood", "lymphoma, nodular sclerosing childhood Hodgkin's", "Childhood Nodular Sclerosis Classic Hodgkin Lymphoma", "Childhood Nodular Sclerosis Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Nodular Sclerosis Classic Hodgkin Lymphoma", "shortest_name_length": 14}
{"curie": "UMLS:C4331426", "names": ["Transient Hyperinsulinism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transient Hyperinsulinism", "shortest_name_length": 25}
{"curie": "MONDO:0004652", "names": ["Bacteria pneumonia", "Pneumonia;bacterial", "pneumonia bacterial", "Bacterial Pneumonia", "Pneumonia bacterial", "Bacterial pneumonia", "PNEUMONIA BACTERIAL", "bacterial pneumonia", "bacterial; pneumonia", "Bacterial Pneumonias", "pneumonia; bacterial", "Pneumonia, Bacterial", "Pneumonias, Bacterial", "Pneumonia bacterial NOS", "gram-negative pneumonia", "Bacterial pneumonia, NOS", "Bacteria caused pneumonia", "Bacterial pneumonia (disorder)", "bacterial pneumonia (diagnosis)", "Unspecified bacterial pneumonia", "Bacterial pneumonia, unspecified", "pneumonia due to other gram-negative bacteria", "Pneumonia due to other gram-negative bacteria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bacterial pneumonia", "shortest_name_length": 18}
{"curie": "UMLS:C1709220", "names": ["Neurotropic Melanoma", "Desmoplastic Neurotropic Melanoma", "Desmoplastic/neurotropic melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Desmoplastic Neurotropic Melanoma", "shortest_name_length": 20}
{"curie": "UMLS:C1167722", "names": ["stage III pancreas cancer", "pancreas cancer, stage III", "stage III pancreatic cancer", "pancreatic cancer, stage III", "Pancreatic carcinoma stage III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic carcinoma stage III", "shortest_name_length": 25}
{"curie": "UMLS:C4682639", "names": ["Stage IIB Primary Peritoneal Cancer", "Stage IIB Primary Peritoneal Cancer AJCC v8", "Stage IIB Primary Peritoneal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Primary Peritoneal Cancer AJCC v8", "shortest_name_length": 35}
{"curie": "MONDO:0008776", "names": ["Hornova Dlushosova syndrome", "amyloidosis of gingiva and conjunctiva with mental retardation", "amyloidosis of gingiva and conjunctiva, with mental retardation", "Amyloidosis of Gingiva and Conjunctiva, with Mental Retardation", "amyloidosis of gingiva and conjunctiva with intellectual disability", "amyloidosis of gingiva and conjunctiva, with intellectual disability", "AMYLOIDOSIS OF GINGIVA AND CONJUNCTIVA WITH IMPAIRED INTELLECTUAL DEVELOPMENT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyloidosis of gingiva and conjunctiva, with intellectual disability", "shortest_name_length": 27}
{"curie": "MONDO:0000500", "names": ["Tongue SCC", "tongue scc", "SCC of Tongue", "scc of tongue", "SCC of the Tongue", "scc of the tongue", "squamous cell carcinoma tongue", "carcinoma cell squamous tongue", "Tongue Squamous Cell Carcinoma", "tongue squamous cell carcinoma", "Squamous Cell Carcinoma of Tongue", "Squamous cell carcinoma of tongue", "squamous cell carcinoma of tongue", "squamous cell carcinoma of the tongue", "Squamous Cell Carcinoma of the Tongue", "Squamous cell carcinoma of the tongue", "SCC - Squamous cell carcinoma of tongue", "Squamous cell carcinoma of tongue (disorder)", "squamous cell carcinoma of tongue (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tongue squamous cell carcinoma", "shortest_name_length": 10}
{"curie": "UMLS:C4526732", "names": ["Lung Adenosquamous Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Adenosquamous Carcinoma by AJCC v7 Stage", "shortest_name_length": 45}
{"curie": "MONDO:0018330", "names": ["appendix mucinous adenocarcinoma", "Appendix Mucinous Adenocarcinoma", "appendiceal mucinous adenocarcinoma", "Appendiceal mucinous adenocarcinoma", "Mucinous adenocarcinoma of appendix", "mucinous adenocarcinoma of appendix", "Mucinous adenocarcinoma of the appendix", "mucinous adenocarcinoma of the appendix", "vermiform appendix mucinous adenocarcinoma", "mucinous adenocarcinoma of appendix (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucinous adenocarcinoma of the appendix", "shortest_name_length": 32}
{"curie": "MONDO:0008933", "names": ["CEPHALIN LIPIDOSIS", "Cephalin Lipidosis", "cephalin lipidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cephalin lipidosis", "shortest_name_length": 18}
{"curie": "MONDO:0016533", "names": ["AApoAII amyloidosis", "apolipoprotein A-II amyloidosis", "familial renal amyloidosis due to apolipoprotein A-II variant", "familial amyloid nephropathy due to apolipoprotein A-II variant", "hereditary renal amyloidosis due to apolipoprotein A-II variant", "hereditary amyloid nephropathy due to apolipoprotein A-II variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "apolipoprotein A-II amyloidosis", "shortest_name_length": 19}
{"curie": "MONDO:0018146", "names": ["aneurysmal telangiectasia", "idiopathic macular telangiectasia type 1", "visible and exudative idiopathic juxtafoveolar retinal telangiectasis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic macular telangiectasia type 1", "shortest_name_length": 25}
{"curie": "UMLS:C5236020", "names": ["Unresectable Renal Pelvis and Ureter Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Renal Pelvis and Ureter Urothelial Carcinoma", "shortest_name_length": 57}
{"curie": "UMLS:C3897760", "names": ["Recurrent Anaplastic Oligoastrocytoma", "Recurrent Childhood Anaplastic Oligoastrocytoma", "recurrent childhood anaplastic oligoastrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Anaplastic Oligoastrocytoma", "shortest_name_length": 37}
{"curie": "UMLS:C1706789", "names": ["Central Ameloblastic Carcinoma", "Ameloblastic Carcinoma-Secondary Type (Dedifferentiated), Intraosseous"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ameloblastic Carcinoma-Secondary Type (Dedifferentiated), Intraosseous", "shortest_name_length": 30}
{"curie": "UMLS:C5237040", "names": ["Recurrent Primary Peritoneal High Grade Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Primary Peritoneal High Grade Serous Adenocarcinoma", "shortest_name_length": 61}
{"curie": "UMLS:C0153254", "names": ["Endocarditis candida", "Candidal endocarditis", "candidal endocarditis", "Candidal endocarditis (disorder)", "candidal endocarditis (diagnosis)", "endocarditis; monilia (manifestation)", "monilia; endocarditis (manifestation)", "endocarditis; candidal (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Candidal endocarditis", "shortest_name_length": 20}
{"curie": "MONDO:0011416", "names": ["GEFSP1", "GEFS+1", "GEFS, Type 1", "Gefs+, type 1", "GEFS+, TYPE 1", "generalized epilepsy with febrile seizures plus 1", "generalised epilepsy with febrile seizures plus 1", "generalized epilepsy with febrile seizures plus type 1", "generalised epilepsy with febrile seizures plus type 1", "generalized epilepsy with febrile seizures plus, type 1", "Generalized Epilepsy With Febrile Seizures Plus, Type 1", "GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "generalized epilepsy with febrile seizures plus, type 1", "shortest_name_length": 6}
{"curie": "MONDO:0015641", "names": ["BIMSE", "benign infantile focal epilepsy with midline spikes and wave during sleep", "benign infantile focal epilepsy with midline spikes and waves during sleep"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign infantile focal epilepsy with midline spikes and wave during sleep", "shortest_name_length": 5}
{"curie": "MONDO:0009779", "names": ["OMOD1", "Omodysplasia 1", "OMODYSPLASIA 1", "omodysplasia 1", "omodysplasia type 1", "Omodysplasia type 1", "Omodysplasia (Maroteaux)", "omodysplasia generalized form", "Omodysplasia generalized form", "OMODYSPLASIA, GENERALIZED FORM", "omodysplasia, generalized form", "Omodysplasia, Generalized Form", "omodysplasia autosomal recessive", "autosomal recessive omodysplasia", "Autosomal recessive omodysplasia", "omodysplasia, autosomal recessive", "Omodysplasia, Autosomal Recessive", "OMODYSPLASIA, AUTOSOMAL RECESSIVE", "Omodysplasia autosomal recessive form", "Micromelic dysplasia dislocation of radius", "Autosomal recessive omodysplasia (disorder)", "Micromelic dysplasia-dislocation of radius syndrome", "micromelic dysplasia-dislocation of radius syndrome", "Micromelic dysplasia, dislocation of radius syndrome", "micromelic dysplasia congenita with dislocation of radius", "Micromelic dysplasia, congenital, with dislocation of radius", "MICROMELIC DYSPLASIA, CONGENITAL, WITH DISLOCATION OF RADIUS", "micromelic dysplasia, congenital, with dislocation of radius"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive omodysplasia", "shortest_name_length": 5}
{"curie": "UMLS:C0948672", "names": ["Venous Lake", "Venous lake", "venous lake", "lakes venous", "Venous lake (disorder)", "Acquired venous hemangioma", "Acquired venous haemangioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Venous lake", "shortest_name_length": 11}
{"curie": "UMLS:C5420408", "names": ["Maxillofacial Osteosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Maxillofacial Osteosarcoma", "shortest_name_length": 26}
{"curie": "MONDO:0020394", "names": ["tunnel subaortic stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tunnel subaortic stenosis", "shortest_name_length": 25}
{"curie": "MONDO:0005683", "names": ["Bruce", "Rock Fever", "Rock fever", "rock fever", "Fever, Rock", "fever malta", "Brucellosis", "Brucelloses", "brucelloses", "brucellosis", "malta fever", "BRUCELLOSIS", "Malta Fever", "Malta fever", "MALTA FEVER", "Cyprus fever", "fever; Malta", "cyprus fever", "Fever, Malta", "FEVER, MALTA", "Malta; fever", "Cyprus Fever", "Fever, Cyprus", "Maltese fever", "fever; Cyprus", "UNDULANT FEVER", "Undulant fever", "Undulant Fever", "MELITOCOCCOSIS", "Bang's disease", "bang's disease", "undulant fever", "FEVER, UNDULANT", "Gibraltar Fever", "Gibraltar fever", "Fever, Undulant", "Fever, Gibraltar", "Gibraltar; fever", "Brucellosis, NOS", "fever; Gibraltar", "Brucella Infection", "Brucella infections", "Brucella; infection", "Brucella Infections", "fever mediterranean", "mediterranean fever", "infection; Brucella", "Infection, Brucella", "Mediterranean fever", "MEDITERRANEAN FEVER", "FEVER, MEDITERRANEAN", "Brucellosis (disorder)", "Unspecified brucellosis", "brucellosis (diagnosis)", "Brucellosis, unspecified", "Infection due to Brucella"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brucellosis", "shortest_name_length": 5}
{"curie": "MONDO:0019230", "names": ["disorder of ornithine or proline metabolism", "inborn disorder of ornithine or proline metabolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of ornithine or proline metabolism", "shortest_name_length": 43}
{"curie": "DOID:0080877", "names": ["Glioblastoma, IDH-Mutant", "Glioblastoma, IDH-mutant", "Astrocytoma, IDH-Mutant, Grade 4", "astrocytoma, IDH-mutant, grade 4", "Astrocytoma, IDH-Mutant, Grade IV"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "astrocytoma, IDH-mutant, grade 4", "shortest_name_length": 24}
{"curie": "MONDO:0005819", "names": ["larynx; tuberculous", "larynx tuberculosis", "Larynx Tuberculosis", "Larynx Tuberculoses", "tuberculosis; larynx", "LARYNX, TUBERCULOSIS", "laryngeal tuberculosis", "tuberculous laryngitis", "laryngitis tuberculous", "Laryngeal Tuberculosis", "Tuberculosis of larynx", "Laryngeal Tuberculoses", "Tuberculous Laryngitis", "Tuberculous laryngitis", "Tuberculosis of Larynx", "Laryngeal tuberculosis", "laryngitis; tuberculous", "Tuberculosis, Laryngeal", "Tuberculoses, Laryngeal", "Tuberculous laryngitis (disorder)", "Tuberculosis (TB) with laryngitis", "tuberculous laryngitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laryngeal tuberculosis", "shortest_name_length": 19}
{"curie": "MONDO:0015736", "names": ["Intermediate congenital NM", "intermediate nemaline myopathy", "Intermediate congenital nemaline myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intermediate nemaline myopathy", "shortest_name_length": 26}
{"curie": "MONDO:0010573", "names": ["Akesson syndrome", "cutis verticis gyrata, thyroid aplasia, and mental retardation", "CUTIS VERTICIS GYRATA, THYROID APLASIA, AND MENTAL RETARDATION", "Cutis Verticis Gyrata, Thyroid Aplasia, and Mental Retardation", "Cutis verticis gyrata-thyroid aplasia-mental retardation syndrome", "cutis verticis gyrata-thyroid aplasia-mental retardation syndrome", "Cutis verticis gyrata, thyroaplasia and mental deficiency syndrome", "cutis verticis gyrata, thyroaplasia and mental deficiency syndrome", "cutis verticis gyrata, thyroid aplasia, and intellectual disability", "cutis verticis gyrata-thyroid aplasia-intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutis verticis gyrata, thyroid aplasia, and intellectual disability", "shortest_name_length": 16}
{"curie": "UMLS:C4551537", "names": ["Stage IVA Cervical Cancer", "Cervical Cancer Stage IVA", "AJCC Stage IVA Cervical Cancer", "FIGO Stage IVA Cervix Carcinoma", "FIGO Stage IVA Cervical Carcinoma", "Stage IVA Cervical Cancer AJCC v7", "Stage IVA Cervical Cancer AJCC v6", "FIGO Stage IVA Carcinoma of Cervix", "FIGO Stage IVA Cervix Uteri Carcinoma", "FIGO Stage IVA Carcinoma of the Cervix", "FIGO Stage IVA Uterine Cervix Carcinoma", "Stage IVA Cervical Cancer AJCC v6 and v7", "FIGO Stage IVA Carcinoma of Cervix Uteri", "FIGO Stage IVA Carcinoma of Uterine Cervix", "FIGO Stage IVA Carcinoma of the Cervix Uteri", "FIGO Stage IVA Carcinoma of the Uterine Cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Cervical Cancer AJCC v6 and v7", "shortest_name_length": 25}
{"curie": "MONDO:0020769", "names": ["MKHK2", "MENKE-HENNEKAM SYNDROME 2", "Menke-Hennekam syndrome 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Menke-Hennekam syndrome 2", "shortest_name_length": 5}
{"curie": "MONDO:0006316", "names": ["Neuroblastic Tumor", "Neuroblastic tumor", "neuroblastic tumor", "Neuroblastic tumour"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuroblastic tumor", "shortest_name_length": 18}
{"curie": "MONDO:0019868", "names": ["mosaic trisomy 10", "Mosaic trisomy 10", "Trisomy 10 mosaicism", "trisomy 10 mosaicism", "Mosaic trisomy type 10", "uniparental disomy of 10", "Uniparental disomy of 10", "Mosaic trisomy 10 syndrome", "Mosaic trisomy chromosome 10", "trisomy 10 mosaicism (diagnosis)", "chromosome 10, uniparental disomy", "Chromosome 10, uniparental disomy of", "Mosaic trisomy 10 syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mosaic trisomy 10", "shortest_name_length": 17}
{"curie": "MONDO:0004205", "names": ["Lymphohistiocytoid Mesothelioma", "lymphohistiocytoid mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphohistiocytoid mesothelioma", "shortest_name_length": 31}
{"curie": "MONDO:0100358", "names": ["ectodermal dysplasia WNT10A related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia WNT10A related", "shortest_name_length": 35}
{"curie": "UMLS:C4727704", "names": ["Refractory Malignant Female Reproductive System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Malignant Female Reproductive System Neoplasm", "shortest_name_length": 56}
{"curie": "UMLS:C4552479", "names": ["Metastatic Anal Squamous Cell Carcinoma", "Anal squamous cell carcinoma metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anal squamous cell carcinoma metastatic", "shortest_name_length": 39}
{"curie": "UMLS:C1519937", "names": ["Vaginal Warty Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Warty Carcinoma", "shortest_name_length": 23}
{"curie": "UMLS:C0852945", "names": ["Malignant pericarditis", "Malignant Pericarditis", "Pericarditis malignant", "Pericarditis, Malignant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pericarditis malignant", "shortest_name_length": 22}
{"curie": "UMLS:C4682891", "names": ["Renal Pelvis Cancer by AJCC v8 Stage", "Renal Pelvis Urothelial Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal Pelvis Cancer by AJCC v8 Stage", "shortest_name_length": 36}
{"curie": "NCIT:C129439", "names": ["Medulloblastoma, Genetically Defined", "Medulloblastoma, Molecularly Defined", "medulloblastoma_molecular_classification", "medulloblastoma molecular classification"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Medulloblastoma, Molecularly Defined", "shortest_name_length": 36}
{"curie": "MONDO:0011640", "names": ["GTPTS", "Genitopatellar Syndrome", "GENITOPATELLAR syndrome", "GENITOPATELLAR SYNDROME", "Genitopatellar syndrome", "genitopatellar syndrome", "Genitopatellar syndrome (disorder)", "absent patellae, scrotal hypoplasia, renal anomalies, Facial Dysmorphism, and mental retardation", "Absent Patellae, Scrotal Hypoplasia, Renal Anomalies, Facial Dysmorphism, and Mental Retardation", "ABSENT PATELLAE, SCROTAL HYPOPLASIA, RENAL ANOMALIES, FACIAL DYSMORPHISM, AND MENTAL RETARDATION", "absent patellae, scrotal hypoplasia, renal anomalies, Facial Dysmorphism, and intellectual disability", "absent patellae-scrotal hypoplasia-renal anomalies-facial dysmorphism-intellectual disability syndrome", "Absent patellae-scrotal hypoplasia-renal anomalies-facial dysmorphism-intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genitopatellar syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0020181", "names": ["mesenchymatous palpebral tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mesenchymatous palpebral tumor", "shortest_name_length": 30}
{"curie": "MONDO:0018135", "names": ["ATN", "OCA1", "ALBINISM I", "Albinism I", "Albinism 1", "oculocutaneous albinism type 1", "Oculocutaneous albinism type 1", "OCULOCUTANEOUS ALBINISM, TYPE I", "Oculocutaneous Albinism, Type I", "Oculocutaneous albinism type 1 (disorder)", "oculocutaneous albinism type 1 (diagnosis)", "oculocutaneous albinism, tyrosinase negative"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculocutaneous albinism type 1", "shortest_name_length": 3}
{"curie": "MONDO:0042963", "names": ["Splenoptosis", "Lien migrans", "Lien mobilis", "lien migrans", "Splenoptoses", "splenoptosis", "lien mobilis", "splenic Ptoses", "splenic ptosis", "Splenic Ptosis", "Splenic Ptoses", "ptosis; spleen", "spleen; ptosis", "ptosis, splenic", "Ptoses, splenic", "Floating Spleen", "Ptosis, Splenic", "Ptoses, Splenic", "drifting spleen", "floating spleen", "Drifting Spleen", "Drifting Spleens", "spleen, drifting", "floating spleens", "spleen, floating", "spleen; floating", "Spleen, Floating", "Wandering spleen", "Displaced Spleen", "floating; spleen", "wandering spleen", "displaced spleen", "Wandering Spleen", "Spleen, Drifting", "Floating Spleens", "drifting spleens", "spleen; wandering", "spleen, displaced", "Wandering Spleens", "Displaced Spleens", "wandering; spleen", "displaced spleens", "Spleen, Displaced", "spleen, wandering", "Spleen, Wandering", "spleens, drifting", "spleens, floating", "Spleens, Drifting", "wandering spleens", "Spleens, Floating", "spleens, wandering", "Spleens, Wandering", "spleens, displaced", "Spleens, Displaced", "Wandering spleen (disorder)", "wandering spleen (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "wandering spleen", "shortest_name_length": 12}
{"curie": "UMLS:C0349613", "names": ["Middle Ear Carcinoma In Situ", "Carcinoma in situ of middle ear", "carcinoma in situ of middle ear", "Carcinoma in situ of middle ear (disorder)", "carcinoma in situ of middle ear (diagnosis)", "auditory neoplasm carcinoma in situ of middle ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carcinoma in situ of middle ear", "shortest_name_length": 28}
{"curie": "MONDO:0006079", "names": ["AC", "Ameloblastic carcinoma", "ameloblastic carcinoma", "Ameloblastic Carcinoma", "carcinoma; ameloblastic", "ameloblastic; carcinoma", "ODONTOMA, AMELOBLASTIC, MALIGNANT", "odontoma, ameloblastic, malignant", "Ameloblastic carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ameloblastic carcinoma", "shortest_name_length": 2}
{"curie": "UMLS:C5238483", "names": ["Locally Advanced Nasopharyngeal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Nasopharyngeal Squamous Cell Carcinoma", "shortest_name_length": 55}
{"curie": "MONDO:0011009", "names": ["MUSCULAR DYSTROPHY, CONGENITAL, WITH SEVERE CENTRAL NERVOUS SYSTEM ATROPHY AND ABSENCE OF LARGE MYELINATED FIBERS", "muscular dystrophy, congenital, with severe central nervous system atrophy and absence of large myelinated fibers", "Muscular Dystrophy, Congenital, with Severe Central Nervous System Atrophy and Absence of Large Myelinated Fibers"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy, congenital, with severe central nervous system atrophy and absence of large myelinated fibers", "shortest_name_length": 113}
{"curie": "MONDO:0016995", "names": ["familial multiple meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial multiple meningioma", "shortest_name_length": 28}
{"curie": "MONDO:0018228", "names": ["Bipartite talus", "bipartite talus", "Bipartite talus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bipartite talus", "shortest_name_length": 15}
{"curie": "MONDO:0008055", "names": ["Myotonia levior", "MYOTONIA LEVIOR", "Thomsen disease", "myotonia levior", "Myotonia Levior", "myotonia Levior", "Thomsen's disease", "Myotonia levior (disorder)", "Thomsen and Becker disease", "myotonia levior (diagnosis)", "myotonia congenita, dominant", "myotonia congenita, autosomal dominant", "Congenital myotonia, autosomal dominant form", "congenital myotonia, autosomal dominant form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myotonia congenita, autosomal dominant", "shortest_name_length": 15}
{"curie": "MONDO:0007258", "names": ["canine teeth, absence of upper permanent", "CANINE TEETH, ABSENCE OF UPPER PERMANENT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canine teeth, absence of upper permanent", "shortest_name_length": 40}
{"curie": "UMLS:C0393638", "names": ["Hyponatremic encephalopathy", "ENCEPHALOPATHY HYPONATREMIC", "Hyponatraemic encephalopathy", "Hyponatremic encephalopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyponatremic encephalopathy", "shortest_name_length": 27}
{"curie": "UMLS:C1262106", "names": ["Neuromuscular toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neuromuscular toxicity", "shortest_name_length": 22}
{"curie": "MONDO:0011685", "names": ["PSAB", "DRUG ADDICTION, SUSCEPTIBILITY TO", "drug addiction, susceptibility to", "polysubstance abuse, susceptibility to", "POLYSUBSTANCE ABUSE, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polysubstance abuse, susceptibility to", "shortest_name_length": 4}
{"curie": "MONDO:0000005", "names": ["alopecia, isolated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alopecia, isolated", "shortest_name_length": 18}
{"curie": "MONDO:0011567", "names": ["CMD1K", "dilated cardiomyopathy 1K", "CARDIOMYOPATHY, DILATED, 1K", "cardiomyopathy, dilated, 1K", "Cardiomyopathy, Dilated, 1K", "dilated cardiomyopathy type 1K"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1K", "shortest_name_length": 5}
{"curie": "MONDO:0014713", "names": ["POROK9", "FDPS porokeratosis (disease)", "POROKERATOSIS 9, MULTIPLE TYPES", "porokeratosis 9, multiple types", "porokeratosis 9, multiple types; POROK9", "porokeratosis (disease) caused by mutation in FDPS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "porokeratosis 9, multiple types", "shortest_name_length": 6}
{"curie": "UMLS:C3888823", "names": ["Intentional product use issue", "Intentional product use issues"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intentional product use issue", "shortest_name_length": 29}
{"curie": "UMLS:C1265926", "names": ["Focal Cytologic Atypia", "Focal cytologic atypia", "Focal cytologic atypia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Focal cytologic atypia", "shortest_name_length": 22}
{"curie": "UMLS:C1709216", "names": ["Neural Tissue Damage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neural Tissue Damage", "shortest_name_length": 20}
{"curie": "MONDO:0019918", "names": ["UPD(21)mat", "maternal uniparental disomy of chromosome 21", "maternal uniparental disomy of chromosome type 21"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maternal uniparental disomy of chromosome 21", "shortest_name_length": 10}
{"curie": "UMLS:C4520733", "names": ["stage II nasopharynx cancer", "Stage II Nasopharyngeal Throat Cancer", "Stage II Nasopharyngeal Cancer AJCC v6", "Stage II Nasopharynx Carcinoma AJCC v6", "Nasopharyngeal Cancer, Stage II AJCC v6", "Stage II Carcinoma of Nasopharynx AJCC v6", "Stage II Nasopharyngeal Carcinoma AJCC v6", "Stage II Carcinoma of the Nasopharynx AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Nasopharyngeal Carcinoma AJCC v6", "shortest_name_length": 27}
{"curie": "MONDO:0020476", "names": ["MTLE-HS", "mesial temporal lobe epilepsy with hippocampal sclerosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mesial temporal lobe epilepsy with hippocampal sclerosis", "shortest_name_length": 7}
{"curie": "UMLS:C4553242", "names": ["Stage II Renal Pelvis Cancer", "Stage II Renal Pelvis Cancer AJCC v8", "Stage II Renal Pelvis Urothelial Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Renal Pelvis Cancer AJCC v8", "shortest_name_length": 28}
{"curie": "MONDO:0008177", "names": ["EMPD", "Paget's Skin Disease", "Paget's skin disease", "paget's skin disease", "Paget disease of skin", "diseases paget's skin", "Paget's Disease of Skin", "Paget's disease of skin", "paget's disease of skin", "Cutaneous Paget's Disease", "cutaneous Paget's disease", "extramammary paget disease", "Paget Disease Extramammary", "extramammary Paget disease", "Extramammary Paget disease", "Extramammary Paget Disease", "Paget disease Extramammary", "Paget's disease of the skin", "Paget Disease, Extramammary", "Paget's Disease of the Skin", "PAGET DISEASE, EXTRAMAMMARY", "Paget disease, extramammary", "Extra Mammary Paget Disease", "Extra-Mammary Paget Disease", "Paget disease, EXTRAMAMMARY", "Extramammary Pagets Disease", "Extramammary, Paget Disease", "extramammary pagets disease", "Pagets Disease, Extramammary", "extra-mammary pagets disease", "Extramammary Paget's Disease", "Extra-Mammary Pagets Disease", "Extramammary Paget's disease", "extramammary Paget's disease", "extramammary paget's disease", "Paget Disease, Extra-Mammary", "Paget Disease, Extra Mammary", "paget's disease extramammary", "Extra-Mammary Paget's Disease", "Extra Mammary Paget's Disease", "extra mammary paget's disease", "Pagets Disease, Extra-Mammary", "extra-mammary paget's disease", "Paget's Disease, Extramammary", "Paget's Disease, Extra Mammary", "Paget's Disease, Extra-Mammary", "extramammary Paget's disease (diagnosis)", "Paget's disease of skin (morphologic abnormality)", "Paget disease, extramammary (except Paget disease of bone)", "Paget's disease, extramammary (except Paget's disease of bone)", "Paget's disease, extramammary (except Paget's disease of bone) (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extramammary Paget disease", "shortest_name_length": 4}
{"curie": "UMLS:C0856623", "names": ["Orofacial edema", "Orofacial oedema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Orofacial edema", "shortest_name_length": 15}
{"curie": "MONDO:0016476", "names": ["Beckwith-Wiedemann syndrome due to CDKN1C mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Beckwith-Wiedemann syndrome due to CDKN1C mutation", "shortest_name_length": 50}
{"curie": "MONDO:0008018", "names": ["MRTES", "muir-torre syndrome", "MUIR-Torre syndrome", "Torré-Muir syndrome", "Muir Torre Syndrome", "Muir-Torré syndrome", "muir torre syndrome", "Muir-Torre syndrome", "Torre-Muir syndrome", "MUIR-TORRE SYNDROME", "torre-muir syndrome", "Muir-Torre Syndrome", "Syndrome, Muir-Torre", "muir torres syndrome", "Torré-Muir syndrome (disorder)", "Muir-Torre syndrome (diagnosis)", "Multiple keratoacanthoma, Muir-Torre type", "multiple keratoacanthoma, Muir-Torre type", "cutaneous sebaceous neoplasms and keratoacanthomas multiple with gastrointestinal and other carcinomas", "CUTANEOUS SEBACEOUS NEOPLASMS AND KERATOACANTHOMAS, MULTIPLE, WITH GASTROINTESTINAL AND OTHER CARCINOMAS", "cutaneous sebaceous neoplasms and keratoacanthomas, multiple, with gastrointestinal and Other carcinomas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Muir-Torre syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C2981609", "names": ["Stage 0 Digestive System Neuroendocrine Tumor", "Stage 0 Gastrointestinal Neuroendocrine Neoplasm", "Stage 0 Digestive System Neuroendocrine Neoplasm", "Stage 0 Digestive System Neuroendocrine Tumor AJCC v7", "Stage 0 Gastrointestinal Neuroendocrine Neoplasm AJCC v7", "Stage 0 Digestive System Neuroendocrine Neoplasm AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Digestive System Neuroendocrine Tumor AJCC v7", "shortest_name_length": 45}
{"curie": "MONDO:0001889", "names": ["Ovarian Failure", "failure ovarian", "ovarian failure", "Ovarian failure", "OVARIAN FAILURE", "dysfunction; ovary", "Ovarian Dysfunction", "Dysfunction ovarian", "DYSFUNCTION OVARIAN", "Ovarian dysfunction", "Dysfunction;ovarian", "ovarian dysfunction", "Ovarian Hypofunction", "ovarian hypofunction", "ovarian insufficiency", "Ovarian Insufficiency", "Other ovarian failure", "Ovarian dysfunction, NOS", "Ovarian failure (disorder)", "Disorder of endocrine ovary", "ovarian failure (diagnosis)", "ovary; functional disturbance", "Unspecified ovarian dysfunction", "Disorder of endocrine ovary, NOS", "Ovarian dysfunction, unspecified", "DISORDERS OF THE ENDOCRINE OVARIES", "Disorder of endocrine ovary (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian dysfunction", "shortest_name_length": 15}
{"curie": "MONDO:0003936", "names": ["Tubular breast cancer", "Tubular Breast Cancer", "tubular breast cancer", "Tubular Breast Carcinoma", "tubular breast carcinoma", "Breast Tubular Carcinoma", "Tubular breast carcinoma", "breast tubular carcinoma", "tubular carcinoma of breast", "Tubular Carcinoma of Breast", "breast tubular adenocarcinoma", "tubular carcinoma of the breast", "ductal tubular breast carcinoma", "Tubular Carcinoma of the Breast", "tubular ductal breast carcinoma", "Invasive Tubular Breast Carcinoma", "invasive tubular breast carcinoma", "Invasive Tubular Carcinoma of Breast", "invasive tubular carcinoma of breast", "Invasive tubular carcinoma of breast", "infiltrating tubular breast carcinoma", "Infiltrating Tubular Breast Carcinoma", "Infiltrating Tubular Carcinoma of Breast", "infiltrating tubular carcinoma of breast", "invasive tubular carcinoma of the breast", "Invasive Tubular Carcinoma of the Breast", "Infiltrating Tubular Carcinoma of the Breast", "infiltrating tubular carcinoma of the breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "invasive tubular breast carcinoma", "shortest_name_length": 21}
{"curie": "UMLS:C5204295", "names": ["Clear Cell Squamous Cell Carcinoma of the Penis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clear Cell Squamous Cell Carcinoma of the Penis", "shortest_name_length": 47}
{"curie": "UMLS:C1332182", "names": ["Anaplastic Large Cell Lymphoma", "Adult Anaplastic Large Cell Lymphoma", "Adult K-1+ Anaplastic Large Cell Lymphoma", "Adult CD30+ Anaplastic Large Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Anaplastic Large Cell Lymphoma", "shortest_name_length": 30}
{"curie": "MONDO:0700102", "names": ["lymphoma, non-human animal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphoma, non-human animal", "shortest_name_length": 26}
{"curie": "MONDO:0008552", "names": ["BDPLT16", "platelet-type bleeding disorder 16", "BLEEDING DISORDER, PLATELET-TYPE, 16", "bleeding disorder, platelet-type, 16", "autosomal dominant Glanzmann thrombasthenia", "Glanzmann Thrombasthenia, Autosomal Dominant", "Glanzmann thrombasthenia, autosomal dominant", "bleeding disorder, platelet-type, 16, autosomal dominant", "autosomal dominant thrombasthenia of Glanzmann and Naegeli", "GLANZMANN THROMBASTHENIA-LIKE WITH MACROTHROMBOCYTOPENIA 1", "Thrombasthenia of Glanzmann and Naegeli, Autosomal Dominant", "thrombasthenia of Glanzmann and Naegeli, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "platelet-type bleeding disorder 16", "shortest_name_length": 7}
{"curie": "UMLS:C4744725", "names": ["Locally Advanced Cervical Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Cervical Adenocarcinoma", "shortest_name_length": 40}
{"curie": "UMLS:C2981412", "names": ["Stage IIIA Gastric Gastrointestinal Stromal Tumor", "Stage IIIA Gastric Gastrointestinal Stromal Tumor AJCC v7", "Stage IIIA Gastric (Stomach) Gastrointestinal Stromal Tumor (GIST)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Gastric Gastrointestinal Stromal Tumor", "shortest_name_length": 49}
{"curie": "UMLS:C0037768", "names": ["Spasmophilia", "Spasmophilias"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spasmophilia", "shortest_name_length": 12}
{"curie": "MONDO:0020540", "names": ["Gynandroblastoma", "Gynandroblastomas", "ovarian gynandroblastoma", "Ovarian Gynandroblastoma", "Ovarian gynandroblastoma", "Gynandroblastoma of ovary", "Gynandroblastoma of Ovary", "Gynandroblastoma of the ovary", "Gynandroblastoma of the Ovary", "Gynandroblastoma of ovary (disorder)", "Gynandroblastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian gynandroblastoma", "shortest_name_length": 16}
{"curie": "MONDO:0002216", "names": ["Brain Sarcoma", "brain sarcoma", "Brain sarcoma", "Sarcoma of Brain", "sarcoma of brain", "sarcoma of the brain", "Intracranial Sarcoma", "Sarcoma of the Brain", "primary brain sarcoma", "Primary Brain Sarcoma", "Primary Intracranial Sarcoma", "sarcoma of brain (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brain sarcoma", "shortest_name_length": 13}
{"curie": "UMLS:C2046647", "names": ["Lung Hodgkin Lymphoma", "hodgkins disease pulmonary", "Pulmonary Hodgkin Lymphoma", "Hodgkin's lymphoma of lung", "hodgkins lymphoma pulmonary", "Primary Lung Hodgkin Lymphoma", "hodgkins disease involving lung", "hodgkins lymphoma involving lung", "Primary Pulmonary Hodgkin Lymphoma", "Hodgkin's lymphoma of lung (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's lymphoma of lung", "shortest_name_length": 21}
{"curie": "MONDO:0009591", "names": ["MLD", "Mld", "ARSA deficiency", "ARSA DEFICIENCY", "ARSA Deficiency", "MLD, adult form", "Deficiency, ARSA", "ARSA Deficiencies", "Greenfield disease", "Greenfield Disease", "Deficiencies, ARSA", "GREENFIELD DISEASE", "MLD, juvenile form", "sulfatide lipidosis", "Greenfield's Disease", "Greenfield's syndrome", "MLD, late infantile form", "Arylsulfatase A deficiency", "ARYLSULFATASE A DEFICIENCY", "Arylsulfatase A Deficiency", "arylsulfatase A deficiency", "Arylsulphatase A deficiency", "Deficiency, Arylsulfatase A", "metachromatic leukodystrophy", "leukodystrophy metachromatic", "Arylsulfatase A Deficiencies", "Deficiencies, Arylsulfatase A", "Pseudoarylsulfatase A Deficiency", "cerebroside sulfatase deficiency", "PSEUDOARYLSULFATASE A DEFICIENCY", "pseudoarylsulfatase A deficiency", "Cerebroside sulfatase deficiency", "Cerebroside Sulfatase Deficiency", "Deficiency, Cerebroside Sulfatase", "Sulfatase Deficiency, Cerebroside", "metachromatic leukoencephalopathy", "ARSA - Arylsulfatase A deficiency", "Cerebroside sulphatase deficiency", "ARSA - Arylsulphatase A deficiency", "Cerebroside Sulfatase Deficiencies", "Adult Metachromatic Leukodystrophy", "Adult metachromatic leukodystrophy", "Adult metachromatic leucodystrophy", "Severe deficiency of arylsulfatase", "Deficiency of cerebroside-sulfatase", "METACHROMATIC LEUKODYSTROPHY, ADULT", "Deficiencies, Cerebroside Sulfatase", "Sulfatase Deficiencies, Cerebroside", "Metachromatic Leukodystrophy, Adult", "Leukodystrophy, Adult Metachromatic", "Infant Metachromatic Leukodystrophy", "metachromatic leukodystrophy, adult", "Severe deficiency of arylsulphatase", "Adult Metachromatic Leukodystrophies", "Metachromatic Leukodystrophy, Infant", "Deficiency of cerebroside-sulphatase", "Leukodystrophy, Metachromatic, Adult", "Infant Metachromatic Leukodystrophies", "Metachromatic Leukodystrophies, Adult", "Leukodystrophies, Adult Metachromatic", "Arylsulfatase A deficiency (disorder)", "metachromatic leukodystrophy, juvenile", "Metachromatic Leukodystrophies, Infant", "Arylsulfatase A deficiency, adult form", "Adult-Type Metachromatic Leukodystrophy", "Metachromatic Leukodystrophy, Adult-Type", "metachromatic leukodystrophy, adult type", "Infant-Type Metachromatic Leukodystrophy", "Metachromatic leucodystrophy, adult type", "Leukodystrophy, Adult-Type Metachromatic", "Metachromatic leukodystrophy, adult form", "Metachromatic leukodystrophy, adult type", "Metachromatic Leukodystrophy, Adult Type", "Adult-Type Metachromatic Leukodystrophies", "Metachromatic Leukodystrophy, Infant-Type", "arylsulfatase A deficiency, juvenile form", "Metachromatic Leukodystrophy, Infant Type", "Metachromatic Leukodystrophies, Adult-Type", "Infant-Type Metachromatic Leukodystrophies", "Leukodystrophies, Adult-Type Metachromatic", "Metachromatic Leukodystrophies, Infant-Type", "metachromatic leukodystrophy, juvenile form", "Late infantile metachromatic leucodystrophy", "Metachromatic Leukodystrophy, Late Infantile", "Metachromatic leukodystrophy, infantile form", "metachromatic leukodystrophy, late infantile", "METACHROMATIC LEUKODYSTROPHY, LATE INFANTILE", "metachromatic leukodystrophy, congenital type", "Metachromatic leucodystrophy, congenital type", "Metachromatic leukodystrophy, congenital type", "cerebral sclerosis diffuse metachromatic form", "Deficiency of cerebroside-sulfatase (disorder)", "Arylsulfatase A deficiency, late infantile form", "cerebral sclerosis, diffuse, metachromatic form", "Metachromatic leucodystrophy, late infantile type", "Metachromatic leukodystrophy, late infantile type", "metachromatic leukodystrophy, late infantile type", "Metachromatic leukodystrophy, late infantile form", "Metachromatic Leukodystrophy, Adult-Type (disorder)", "Metachromatic leukodystrophy, adult type (disorder)", "metachromatic leukodystrophy, adult type (diagnosis)", "Metachromatic leukodystrophy, congenital type (disorder)", "metachromatic leukodystrophy, congenital type (diagnosis)", "Metachromatic leukodystrophy, late infantile type (disorder)", "metachromatic leukodystrophy, late infantile type (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metachromatic leukodystrophy, juvenile form", "shortest_name_length": 3}
{"curie": "UMLS:C2363888", "names": ["Intestinal anastomosis complication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal anastomosis complication", "shortest_name_length": 35}
{"curie": "MONDO:0003686", "names": ["Apocrine Tumor", "Apocrine tumor", "apocrine tumor", "Apocrine Neoplasm", "apocrine neoplasm", "Apocrine Skin Tumor", "apocrine skin tumor", "apocrine tumor of skin", "apocrine skin neoplasm", "Apocrine Skin Neoplasm", "Apocrine Tumor of Skin", "Apocrine Neoplasm of Skin", "apocrine neoplasm of skin", "Apocrine Tumor of the Skin", "apocrine sweat gland tumor", "apocrine tumor of the skin", "Apocrine Neoplasm of the Skin", "apocrine neoplasm of the skin", "tumor of apocrine sweat gland", "apocrine sweat gland neoplasm", "neoplasm of apocrine sweat gland", "apocrine sweat gland neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "apocrine sweat gland neoplasm", "shortest_name_length": 14}
{"curie": "UMLS:C0263888", "names": ["back disorder", "Back disorder", "Disorder;back", "BACK DISORDER", "back disorders", "disorder of back", "Disorder of back", "Back disorder NOS", "Disorder of back, NOS", "Disorder of back (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Back disorder", "shortest_name_length": 13}
{"curie": "UMLS:C0751011", "names": ["Right Hemisphere, Cerebral Infarction", "Cerebral Infarction, Right Hemisphere", "Right Hemisphere, Infarction, Cerebral", "Cerebral, Right Hemisphere, Infarction", "Infarction, Cerebral, Right Hemisphere", "Infarction, Right Hemisphere, Cerebral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebral Infarction, Right Hemisphere", "shortest_name_length": 37}
{"curie": "MONDO:0008067", "names": ["NPCA2", "Npca2", "NASOPHARYNGEAL CARCINOMA, SUSCEPTIBILITY TO, 2", "nasopharyngeal carcinoma, susceptibility to, 2", "nasopharyngeal carcinoma, susceptibility to, type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasopharyngeal carcinoma, susceptibility to, 2", "shortest_name_length": 5}
{"curie": "MONDO:0014791", "names": ["LLS", "LLs", "Luscan-Lumish syndrome", "LUSCAN-LUMISH SYNDROME", "Luscan-Lumish syndrome; LLs", "SETD2-related overgrowth syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Luscan-Lumish syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0004275", "names": ["Paget Osteosarcoma", "Paget osteosarcoma", "Paget; osteosarcoma", "Paget's Osteosarcoma", "Paget's osteosarcoma", "osteosarcoma in Paget disease of bone", "Osteosarcoma in Paget disease of bone", "Osteosarcoma in Paget's disease of bone", "osteosarcoma; in Paget's disease of bone", "osteosarcoma arising in osteitis deformans", "Osteosarcoma Arising in Osteitis Deformans", "osteosarcoma arising in bone Paget disease", "osteosarcoma arising in bone Paget's disease", "Osteosarcoma Arising in Bone Paget's Disease", "Osteosarcoma Arising in Paget Disease of Bone", "osteosarcoma arising in Paget disease of bone", "osteosarcoma arising in Paget's disease of bone", "Osteosarcoma Arising in Osseous Paget's Disease", "Osteosarcoma Arising in osseous Paget's disease", "Osteosarcoma Arising in Paget's Disease of Bone", "osteosarcoma arising in osseous Paget's disease", "osteosarcoma in Paget disease of bone (diagnosis)", "Osteosarcoma in Paget's disease of bone (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteosarcoma arising in bone Paget disease", "shortest_name_length": 18}
{"curie": "MONDO:0022662", "names": ["carpo tarsal osteolysis recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carpo tarsal osteolysis recessive", "shortest_name_length": 33}
{"curie": "MONDO:0800138", "names": ["multisystem autoimmune disease due to IKAROS gain of function"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multisystem autoimmune disease due to IKAROS gain of function", "shortest_name_length": 61}
{"curie": "UMLS:C0280344", "names": ["Stage I Lip Basal Cell Cancer", "Stage I Lip Basal Cell Carcinoma", "lip basal cell carcinoma, stage I", "Stage I Basal Cell Carcinoma of Lip", "Stage I Basal Cell Carcinoma of the Lip", "stage I basal cell carcinoma of the lip", "basal cell carcinoma of the lip, stage I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Lip Basal Cell Carcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0030528", "names": ["IMD93", "immunodeficiency and hypertrophic cardiomyopathy", "immunodeficiency 93 and hypertrophic cardiomyopathy", "IMMUNODEFICIENCY 93 AND HYPERTROPHIC CARDIOMYOPATHY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 93 and hypertrophic cardiomyopathy", "shortest_name_length": 5}
{"curie": "UMLS:C0935681", "names": ["nonhematologic cancer", "Non-Hematologic Cancer", "Non-Hematologic Malignancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Hematologic Malignancy", "shortest_name_length": 21}
{"curie": "UMLS:C5235894", "names": ["Advanced Adenoid Cystic Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Adenoid Cystic Carcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C2936381", "names": ["Neointima Formation", "Formation, Neointima"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neointima Formation", "shortest_name_length": 19}
{"curie": "UMLS:C3897518", "names": ["Stage IVA Thyroid Gland Papillary Cancer", "Stage IVA Thyroid Gland Papillary Carcinoma", "Stage IVA Thyroid Gland Papillary Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Thyroid Gland Papillary Carcinoma AJCC v7", "shortest_name_length": 40}
{"curie": "MONDO:0003727", "names": ["Zoophobia", "zoophobia", "ANIMAL FEAR", "phobia animal", "animal phobia", "Animal phobia", "Animal Phobia", "Animal phobias", "animal; phobia", "animal phobias", "phobia; animal", "Phobia, animals", "fear of animals", "Fear of animals", "Zoophobia (finding)", "zoophobia (finding)", "fear of animals (finding)", "Fear of animals (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "animal phobia", "shortest_name_length": 9}
{"curie": "MONDO:0032934", "names": ["GUBS", "GENITOURINARY AND/OR BRAIN MALFORMATION SYNDROME", "genitourinary and/or brain malformation syndrome", "genitourinary and/or/brain malformation syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genitourinary and/or brain malformation syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0100130", "names": ["RDS", "ards", "ARDS", "a r d s", "a.r.d.s.", "wet lung", "A.R.D.S.", "Adult RDS", "adult rds", "adult RDS", "adult ARDS", "Shock lung", "Shock Lung", "SHOCK LUNG", "shock lung", "danang lung", "DaNang lung", "shock; lung", "lung; shock", "Lung, Shock", "Vietnam lung", "traumatic lung", "wet lung syndrome", "WET LUNG SYNDROME", "Traumatic wet lung", "Shock-lung syndrome", "syndrome; shock-lung", "shock-lung; syndrome", "Congestive atelectasis", "Wet-lung syndrome, adult", "adult respiratory syndrome", "SYNDROME ADULT RESPIRATORY", "Newborn respiratory distress", "Respiratory Distress Syndrome", "Respiratory distress neonatal", "neonatal respiratory distress", "Respiratory distress syndrome", "Neonatal respiratory distress", "distress respiratory neonatal", "RESPIRATORY DISTRESS SYNDROME", "distress syndrome; respiratory", "adult hyaline membrane disease", "Distress Syndrome, Respiratory", "respiratory distress; syndrome", "syndrome; respiratory distress", "Adult hyaline membrane disease", "Infantile respiratory distress", "Syndrome, Respiratory Distress", "Respiratory distress, neonatal", "respiratory; distress syndrome", "Respiratory distress (newborn)", "Respiratory Distress Syndromes", "Non-cardiogenic pulmonary edema", "Distress Syndromes, Respiratory", "ADULT RESPIRATORY DISTRESS SYNDR", "Adult respiratory stress syndrome", "Pulmonary capillary leak syndrome", "hyaline; disease, membrane, adult", "ADULT RESPIRATORY STRESS SYNDROME", "Syndrome adult respiratory distress", "RESPIRATORY DISTRESS SYNDROME ACUTE", "Acute Respiratory Distress Syndrome", "Syndrome respiratory distress adult", "adult respiratory distress syndrome", "Respiratory distress syndrome adult", "ADULT RESPIRATORY DISTRESS SYNDROME", "SYNDROME ADULT RESPIRATORY DISTRESS", "acute respiratory distress syndrome", "RESPIRATORY DISTRESS SYNDROME ADULT", "Acute respiratory distress syndrome", "Adult respiratory distress syndrome", "SYNDROME RESPIRATORY DISTRESS ADULT", "Adult Respiratory Distress Syndrome", "RESPIRATORY DISTRESS SYNDROME, ADULT", "DISTRESS RESPIRATORY SYNDROME ADULTS", "Respiratory distress syndrome, Adult", "Respiratory Distress Syndrome, Adult", "respiratory distress syndrome, adult", "Respiratory distress syndrome, adult", "syndrome; respiratory distress, adult", "distress syndrome; respiratory, adult", "respiratory distress; syndrome, adult", "POSTTRAUMATIC PULMONARY INSUFFICIENCY", "distress; respiratory syndrome, adult", "distress; respiratory, syndrome, adult", "post traumatic pulmonary insufficiency", "respiratory; distress, syndrome, adult", "Post-traumatic pulmonary insufficiency", "Acquired respiratory distress syndrome", "Respiratory distress syndrome (finding)", "Neonatal respiratory distress (finding)", "posttraumatic respiratory insufficiency", "Adult respiratory distress syndrome, NOS", "Pulmonary insufficiency following trauma", "adult respiratory distress syndrome, ARDS", "adult acute respiratory distress syndrome", "ARDS - Adult respiratory distress syndrome", "pulmonary; insufficiency, following trauma", "ARDs - Acute respiratory distress syndrome", "insufficiency; pulmonary, following trauma", "adult respiratory distress syndrome (ARDS)", "Acute respiratory distress syndrome (disorder)", "post traumatic pulmonary insufficiency (diagnosis)", "Pulmonary insufficiency following trauma (disorder)", "adult respiratory distress syndrome (ARDS) (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult acute respiratory distress syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C4524190", "names": ["HGBL with MYC and BCL2 and/or BCL6 Rearrangements", "High Grade B-Cell Lymphoma with MYC and BCL2 and/or BCL6 Rearrangements", "High grade B-cell lymphoma with MYC and BCL2 and/or BCL6 rearrangements", "High-grade B-cell lymphoma, with MYC and BCL2 and/or BCL6 rearrangements", "High grade B-cell lymphoma with MYC and BCL2 and/or BCL6 rearrangements (disorder)", "High grade B-cell lymphoma with MYC and BCL2 and/or BCL6 rearrangements (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High grade B-cell lymphoma with MYC and BCL2 and/or BCL6 rearrangements", "shortest_name_length": 49}
{"curie": "UMLS:C4525062", "names": ["Recurrent Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Lymphoma", "shortest_name_length": 18}
{"curie": "UMLS:C5447389", "names": ["Functioning Lung Carcinoid Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Functioning Lung Carcinoid Tumor", "shortest_name_length": 32}
{"curie": "MONDO:0019848", "names": ["posterior hypospadias", "perineal, scrotal or penoscrotal hypospadias"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "posterior hypospadias", "shortest_name_length": 21}
{"curie": "MONDO:0008324", "names": ["pseudoarthrogryposis", "Pseudoarthrogryposis", "PSEUDOARTHROGRYPOSIS", "ankylosis at elbow and knee", "Ankylosis at Elbow and Knee", "ANKYLOSIS AT ELBOW AND KNEE", "hereditary congenital rigidity of elbows and knees", "HEREDITARY CONGENITAL RIGIDITY OF ELBOWS AND KNEES", "Hereditary Congenital Rigidity of Elbows and Knees"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudoarthrogryposis", "shortest_name_length": 20}
{"curie": "UMLS:C1335171", "names": ["Ovarian Myxoma", "Myxoma of Ovary", "Myxoma of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Myxoma", "shortest_name_length": 14}
{"curie": "MONDO:0100372", "names": ["disorder of peroxisomal transporter", "disorder of peroxisomal transporter defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of peroxisomal transporter", "shortest_name_length": 35}
{"curie": "UMLS:C1332491", "names": ["Benign Diencephalic Tumor", "Benign Diencephalic Neoplasm", "Benign Tumor of Diencephalon", "Benign Diencephalic Neoplasms", "Benign Neoplasm of Diencephalon", "Benign Tumor of the Diencephalon", "Benign Neoplasm of the Diencephalon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Diencephalic Neoplasm", "shortest_name_length": 25}
{"curie": "UMLS:C5555150", "names": ["Bone Hibernoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone Hibernoma", "shortest_name_length": 14}
{"curie": "UMLS:C0919976", "names": ["Renal cancer metastatic", "renal cancer metastatic", "metastatic renal cancer", "cancer metastatic renal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal cancer metastatic", "shortest_name_length": 23}
{"curie": "UMLS:C1336967", "names": ["Virus-Related Carcinoma", "Virus Related Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Virus-Related Carcinoma", "shortest_name_length": 23}
{"curie": "UMLS:C0854983", "names": ["Lung adenocarcinoma recurrent", "Recurrent Lung Adenocarcinoma", "Lung Adenocarcinoma, Recurrent", "Adenocarcinoma of lung recurrent", "Recurrent Adenocarcinoma of Lung", "Recurrent Adenocarcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung adenocarcinoma recurrent", "shortest_name_length": 29}
{"curie": "MONDO:0005168", "names": ["neoplasm of immature B and T cells"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplasm of immature B and T cells", "shortest_name_length": 34}
{"curie": "UMLS:C0079765", "names": ["Grade 1", "FSC lymphoma", "NLPD lymphoma", "NPDL lymphoma", "nodular PDL lymphoma", "PDL, nodular lymphocytic", "Grade 1 Follicular Lymphoma", "Follicular Lymphoma Grade 1", "Follicular lymphoma grade I", "grade 1 follicular lymphoma", "Grade I Follicular Lymphoma", "Follicular lymphoma, grade 1", "Follicular Lymphoma, Grade 1", "Lymphoma, Follicular, Grade 1", "Lymphoma, Small Lymphoid, Follicular", "Lymphoblastic lymphosarcoma, nodular", "Small Follicular Center Cell Lymphoma", "Small Follicular Center-Cell Lymphoma", "follicular small cleaved cell lymphoma", "Lymphoma, Small Follicular Center-Cell", "Follicular Small Cleaved Cell Lymphoma", "Lymphoma, Small Follicular Center Cell", "Small Cleaved Cell Lymphoma, Follicular", "small cleaved cell lymphoma, follicular", "Lymphoblastic lymphosarcoma, follicular", "Small Cleaved-Cell Lymphoma, Follicular", "Follicular lymphoma, small cleaved cell", "lymphoma, follicular small cleaved cell", "grade 1 follicular lymphoma (diagnosis)", "Lymphoma, Small Cleaved-Cell, Follicular", "Lymphoma, Small Cleaved Cell, Follicular", "small cell; lymphoma, cleaved, follicular", "lymphoma; follicular, small cell, cleaved", "lymphoma; small cell, cleaved, follicular", "follicular; lymphoma, small cell, cleaved", "WHO Follicular Lymphoma Histologic Grade 1", "grade I follicular small cleaved cell lymphoma", "Grade I Follicular Small Cleaved Cell Lymphoma", "Follicular malignant lymphoma, small cleaved cell", "Poorly Differentiated Nodular Lymphocytic Lymphoma", "Follicular malignant lymphoma - small cleaved cell", "Malignant lymphoma, small cleaved cell, follicular", "nodular poorly-differentiated lymphocytic lymphoma", "poorly-differentiated lymphoma, nodular lymphocytic", "nodular lymphocytic, poorly-differentiated lymphoma", "Follicular non-Hodgkin lymphoma, small cleaved cell", "Follicular non-Hodgkin's small cleaved cell lymphoma", "lymphoma, nodular lymphocytic, poorly-differentiated", "Lymphocytic lymphoma, poorly differentiated, nodular", "Lymphocytic Lymphoma, Nodular, Poorly Differentiated", "Lymphocytic Lymphoma, Nodular, Poorly-Differentiated", "Follicular non-Hodgkin's lymphoma, small cleaved cell", "nodular; lymphoma, lymphocytic, poorly differentiated", "Lymphoma, Lymphocytic, Nodular, Poorly Differentiated", "follicular non-Hodgkin's lymphoma, small cleaved cell", "lymphocytic; lymphoma, nodular, poorly differentiated", "Small cleaved cell, follicular non-Hodgkin's lymphoma", "lymphoma; lymphocytic, nodular, poorly differentiated", "Lymphoma, Lymphocytic, Nodular, Poorly-Differentiated", "lymphoma; nodular, lymphocytic, poorly differentiated", "malignant neoplasm nodular lymphoma follicular grade 1", "Follicular lymphoma, grade 1 (morphologic abnormality)", "Lymphocytic lymphoma, poorly differentiated, follicular", "Follicular malignant lymphoma - small cleaved cell (disorder)", "Follicular malignant lymphoma, small cleaved cell (diagnosis)", "Malignant lymphoma, lymphocytic, poorly differentiated, nodular", "Follicular non-Hodgkin's lymphoma, small cleaved cell (disorder)", "Follicular non-Hodgkin's lymphoma, small cleaved cell (clinical)", "Malignant lymphoma, follicular, predominately small cleaved cell", "follicular non-Hodgkin's lymphoma, small cleaved cell (diagnosis)", "Malignant lymphoma, lymphocytic, poorly differentiated, follicular", "[M]Malignant lymphoma, lymphocytic, poorly differentiated, nodular", "Malignant lymphoma, lymphocytic, poorly differentiated, nodular (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoma, Small Cleaved-Cell, Follicular", "shortest_name_length": 7}
{"curie": "MONDO:0010085", "names": ["Schilder", "Flatau-Schilder", "Schilder Disease", "schilder disease", "SCHILDER DISEASE", "Schilder disease", "disease schilders", "Diffuse sclerosis", "Schilders Disease", "Disease, Schilder", "diffuse sclerosis", "schilders disease", "schilder's disease", "sclerosis; diffuse", "Schilder's Disease", "diffuse; sclerosis", "Schilder's disease", "SCLEROSIS, DIFFUSE", "Disease, Schilder's", "Cerebral poliodystrophy", "poliodystrophia cerebri", "Poliodystrophia cerebri", "Poliodystrophia Cerebri", "Encephalitis Periaxialis", "encephalitis periaxialis", "Diffuse Cerebral Scleroses", "diffuse cerebral sclerosis", "Diffuse cerebral sclerosis", "Diffuse Cerebral Sclerosis", "LEUKOENCEPHALITIS, SUBACUTE", "Cerebral Sclerosis, Diffuse", "Sclerosis, Diffuse Cerebral", "Cerebral sclerosis, Diffuse", "LEUKODYSTROPHY, SUDANOPHILIC", "Schilder's disease (disorder)", "Schilder's disease (diagnosis)", "SUDANOPHILIC cerebral sclerosis", "SUDANOPHILIC CEREBRAL SCLEROSIS", "Sudanophilic Cerebral Sclerosis", "SCLEROSIS, SUDANOPHILIC CEREBRAL", "Encephalitis Periaxialis Diffusa", "Myelinoclastic Diffuse Sclerosis", "Encephalitis periaxialis diffusa", "Myelinoclastic diffuse sclerosis", "Myelinoclastic Diffuse Scleroses", "Sclerosis, Myelinoclastic Diffuse", "Encephalitis periaxialis, diffusa", "ENCEPHALITIS, PERIAXIALIS DIFFUSA", "Scleroses, Myelinoclastic Diffuse", "Diffuse Sclerosis, Myelinoclastic", "Diffuse Scleroses, Myelinoclastic", "periaxialis; encephalitis, diffusa", "encephalitis; periaxialis, diffusa", "Encephalitis periaxialis, Schilder's", "Encephalitis Periaxialis Concentrica", "Diffuse Cerebral Sclerosis of Schilder", "Progressive infantile cortical poliodystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Schilder disease", "shortest_name_length": 8}
{"curie": "UMLS:C0281393", "names": ["AIDS Related Diffuse Mixed Cell Lymphoma", "AIDS-Related Diffuse Mixed Cell Lymphoma", "AIDS-related diffuse mixed cell lymphoma", "diffuse mixed cell lymphoma, AIDS-related", "AIDS Associated Diffuse Mixed Cell Lymphoma", "AIDS-associated diffuse mixed cell lymphoma", "AIDS-Associated Diffuse Mixed Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Diffuse Mixed Cell Lymphoma", "shortest_name_length": 40}
{"curie": "UMLS:C1167737", "names": ["Small Intestine Cancer Stage III", "Stage III Small Intestinal Cancer", "Stage III Small Intestine Carcinoma", "Small intestine carcinoma stage III", "Stage III Small Intestinal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small intestine carcinoma stage III", "shortest_name_length": 32}
{"curie": "UMLS:C5394830", "names": ["Sinonasal glomangiopericytoma", "Sinonasal Glomangiopericytoma", "Glomangiopericytoma of nasal sinus", "Sinonasal Hemangiopericytoma-Like Tumor", "Glomangiopericytoma of nasal sinus (disorder)", "Glomangiopericytoma of nasal sinus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal glomangiopericytoma", "shortest_name_length": 29}
{"curie": "MONDO:0014242", "names": ["VMLDS2", "Van Maldergem syndrome 2", "van Maldergem syndrome 2", "VAN MALDERGEM SYNDROME 2", "VAN Maldergem syndrome 2", "Van Maldergem Syndrome 2", "FAT4 van Maldergem syndrome", "Van Maldergem syndrome type 2", "van Maldergem syndrome caused by mutation in FAT4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "van Maldergem syndrome 2", "shortest_name_length": 6}
{"curie": "MONDO:0012808", "names": ["CMH23", "CMD1AA", "dilated cardiomyopathy 1AA", "CARDIOMYOPATHY, DILATED, 1AA", "Cardiomyopathy, Dilated, 1AA", "dilated cardiomyopathy type 1AA", "ACTN2 familial isolated dilated cardiomyopathy", "cardiomyopathy, dilated, 1AA, with or without LVNC", "cardiomyopathy, hypertrophic, 23, with or without LVNC", "familial isolated dilated cardiomyopathy caused by mutation in ACTN2", "dilated cardiomyopathy 1AA with or without left ventricular noncompaction", "CARDIOMYOPATHY, DILATED, 1AA, WITH OR WITHOUT LEFT VENTRICULAR NONCOMPACTION", "cardiomyopathy, dilated, 1AA, with or without left ventricular noncompaction", "CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 23, WITH OR WITHOUT VENTRICULAR NONCOMPACTION", "cardiomyopathy, familial hypertrophic, 23, with or without ventricular noncompaction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1AA", "shortest_name_length": 5}
{"curie": "UMLS:C0334040", "names": ["OSTEOSIS", "Osteosis", "osteosis", "Osteosis, NOS", "Bone Metaplasia", "Osseous metaplasia", "Osseous Metaplasia", "OSSEOUS METAPLASIA", "osseous metaplasia", "OSSEOUS METAPLASIAS", "Osseous Metaplasias", "Metaplasia, osseous", "Osseous metaplasia, NOS", "metaplastic ossification", "Metaplastic ossification", "Extraskeletal ossification", "extraskeletal ossification", "Metaplastic ossification, NOS", "Extraskeletal ossification, NOS", "Osseous metaplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Osseous metaplasia", "shortest_name_length": 8}
{"curie": "MONDO:0002517", "names": ["tenosynovitis ankle/foot", "tenosynovitis of ankle/foot", "Tenosynovitis of foot and ankle", "tenosynovitis of foot and ankle", "tenosynovitis of ankle/foot (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tenosynovitis of foot and ankle", "shortest_name_length": 24}
{"curie": "MONDO:0011491", "names": ["EIG7", "EJM2", "epilepsy, juvenile myoclonic", "MYOCLONIC EPILEPSY, JUVENILE, 2", "myoclonic epilepsy, juvenile, 2", "idiopathic generalized epilepsy 7", "epilepsy, idiopathic generalized, susceptibility to, 7", "EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, idiopathic generalized, susceptibility to, 7", "shortest_name_length": 4}
{"curie": "UMLS:C0278735", "names": ["Stage I Lymphoblastic Lymphoma", "NHL, lymphoblastic stage I childhood", "Childhood Lymphoblastic Lymphoma Stage I", "stage I childhood lymphoblastic lymphoma", "stage I lymphoblastic childhood lymphoma", "Pediatric Lymphoblastic Lymphoma Stage I", "Stage I Pediatric Lymphoblastic Lymphoma", "Stage I Childhood Lymphoblastic Lymphoma", "Stage I Childhood Precursor Lymphoblastic Lymphoma", "Ann Arbor Stage I Childhood Lymphoblastic Lymphoma", "lymphoblastic stage I non-Hodgkin's lymphoma, childhood", "pediatric lymphoblastic non-Hodgkin's lymphoma, stage I", "childhood non-Hodgkin's lymphoma, lymphoblastic stage I", "non-Hodgkin's lymphoma, lymphoblastic stage I childhood", "lymphoma, non-Hodgkin's, lymphoblastic stage I childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Childhood Lymphoblastic Lymphoma", "shortest_name_length": 30}
{"curie": "MONDO:0037149", "names": ["HSD10 disease, atypical type", "HSD10 deficiency, atypical type", "Syndromic X-linked intellectual disability type 10", "X-linked intellectual disability-choreoathetosis-abnormal behavior syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HSD10 disease, atypical type", "shortest_name_length": 28}
{"curie": "MONDO:0014293", "names": ["DFNA58", "autosomal dominant deafness 58", "deafness, autosomal dominant 58", "DEAFNESS, AUTOSOMAL DOMINANT 58", "autosomal dominant nonsyndromic deafness 58", "autosomal dominant nonsyndromic hearing loss 58", "autosomal dominant nonsyndromic deafness type 58"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 58", "shortest_name_length": 6}
{"curie": "UMLS:C4688007", "names": ["Platinum-Resistant Ovarian Cancer", "Platinum-Resistant Ovarian Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Platinum-Resistant Ovarian Carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0004513", "names": ["Pleomorphic rhabdomyosarcoma", "adult pleomorphic rhabdomyosarcoma", "Adult Pleomorphic Rhabdomyosarcoma", "pleomorphic rhabdomyosarcoma of adults", "adult type pleomorphic rhabdomyosarcoma", "pleomorphic, adult type rhabdomyosarcoma", "Pleomorphic rhabdomyosarcoma, adult type", "adult type pleomorphic rhabdomyosarcoma (diagnosis)", "Pleomorphic rhabdomyosarcoma (morphologic abnormality)", "malignant myosarcoma rhabdomyosarcoma pleomorphic adult type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult pleomorphic rhabdomyosarcoma", "shortest_name_length": 28}
{"curie": "UMLS:C1333870", "names": ["Grade I Rectal Adenocarcinoma", "Grade 1 Rectal Adenocarcinoma", "Well Differentiated Rectal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade 1 Rectal Adenocarcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0017145", "names": ["beta-thalassemia and related diseases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "beta-thalassemia and related diseases", "shortest_name_length": 37}
{"curie": "UMLS:C1096691", "names": ["BK virus infection", "BK Virus Infection", "BK Viral Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "BK virus infection", "shortest_name_length": 18}
{"curie": "UMLS:C0280352", "names": ["Stage II Mouth Adenoid Cystic Carcinoma", "Stage II Oral Cavity Adenoid Cystic Cancer", "Stage II Adenoid Cystic Carcinoma of Mouth", "Stage II Oral Cavity Adenoid Cystic Carcinoma", "Stage II Adenoid Cystic Carcinoma of the Mouth", "oral cavity adenoid cystic carcinoma, stage II", "Stage II Adenoid Cystic Carcinoma of Oral Cavity", "Stage II Adenoid Cystic Carcinoma of the Oral Cavity", "stage II adenoid cystic carcinoma of the oral cavity", "Adenoid cystic carcinoma of the oral cavity stage II", "Stage II Oral Cavity Adenoid Cystic Carcinoma AJCC v7", "Stage II Oral Cavity Adenoid Cystic Carcinoma AJCC v6", "adenoid cystic carcinoma of the oral cavity, stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenoid cystic carcinoma of the oral cavity stage II", "shortest_name_length": 39}
{"curie": "MONDO:0001921", "names": ["Persistent mucosal disease", "Chronic atticoantral disease", "chronic atticoantral disease", "Chronic atticoantral disease (diagnosis)", "disease (or disorder); atticoantral, chronic", "chronic atticoantral suppurative otitis media", "Chronic atticoantral suppurative otitis media", "Chronic suppurative otitis media - atticoantral", "otitis; media, chronic, suppurative, atticoantral", "Chronic atticoantral suppurative otitis media (disorder)", "chronic atticoantral suppurative otitis media (diagnosis)", "Chronic atticoantral suppurative otitis media, unspecified ear", "Persistent mucosal disease with posterior or superior marginal perforation of ear drum", "Chronic atticoantral disease with posterior or superior marginal perforation of ear drum", "Persistent mucosal disease with posterior AND/OR superior marginal perforation of ear drum", "Chronic atticoantral disease with posterior AND/OR superior marginal perforation of ear drum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic atticoantral disease", "shortest_name_length": 26}
{"curie": "MONDO:0015492", "names": ["AAV", "Pauci-Immune Vasculitis", "Pauci Immune Vasculitis", "Vasculitis, Pauci-Immune", "ANCA positive vasculitis", "Pauci-Immune Vasculitides", "ANCA associated vasculitis", "Vasculitides, Pauci-Immune", "ANCA-Associated Vasculitis", "ANCA Associated Vasculitis", "ANCA-associated vasculitis", "ANCA-Associated Vasculitide", "Vasculitis, ANCA-Associated", "ANCA Associated Vasculitides", "ANCA-Associated Vasculitides", "Vasculitide, ANCA-Associated", "Vasculitides, ANCA-Associated", "Antineutrophil cytoplasmic antibody positive vasculitis", "Antineutrophilic cytoplasmic antibody [ANCA] vasculitis", "antineutrophil cytoplasmic antibody positive vasculitis", "Antineutrophil cytoplasmic antibody-associated vasculitis", "antineutrophil cytoplasmic antibody-associated vasculitis", "Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis", "Anti-neutrophil cytoplasmic antibody-associated vasculitis", "Anti Neutrophil Cytoplasmic Antibody Associated Vasculitis", "anti-neutrophil cytoplasmic antibody-associated vasculitis", "Antineutrophil cytoplasmic antibody (ANCA) positive vasculitis", "Antineutrophil cytoplasmic antibody positive vasculitis (disorder)", "antineutrophil cytoplasmic antibody positive vasculitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anti-neutrophil cytoplasmic antibody-associated vasculitis", "shortest_name_length": 3}
{"curie": "MONDO:0005090", "names": ["SCZD", "Schizophrenia", "SCHIZOPHRENIA", "schizophrenia", "schizophrenias", "Schizophrenias", "SCHIZOPHRENIAS", "schizophrenia-1", "schizophrenia 12", "Dementia Praecox", "Dementia praecox", "dementia praecox", "praecox; dementia", "Schizophrenia NOS", "schizophrenia type", "type schizophrenia", "Schizophrenia, NOS", "schizophrenia types", "Schizophrenic Disorder", "disorder schizophrenic", "schizophrenic disorder", "schizophrenia disorder", "disorder schizophrenia", "obsolete_schizophrenia", "Disorder, Schizophrenic", "schizophrenic disorders", "Schizophrenia all types", "Schizophrenic disorders", "schizophrenia (disease)", "Schizophrenic Disorders", "disorders schizophrenia", "disorders schizophrenic", "schizophrenia disorders", "schizoaffective disorder", "Disorders, Schizophrenic", "disorders schizophrenics", "Schizophrenia (disorder)", "Unspecified schizophrenia", "schizophrenia (diagnosis)", "unspecified schizophrenia", "Schizophrenia, unspecified", "schizophrenia, susceptibility to", "Schizophrenic disorders (disorder)", "schizophrenia disorders (diagnosis)", "Unspecified schizophrenia, unspecified", "Unspecified schizophrenia, unspecified state", "SCHIZOPHRENIA WITH OR WITHOUT AN AFFECTIVE DISORDER", "schizophrenia with or without an affective disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schizophrenia", "shortest_name_length": 4}
{"curie": "UMLS:C0399602", "names": ["leukoplakia lip", "lip leukoplakia", "Leukoplakia of Lip", "Leucoplakia of lips", "Leukoplakia of lips", "Leucokeratosis of lip", "Leukokeratosis of lip", "leukokeratosis of lip", "oral leukoplakia of lips", "Leukoplakia of lips (disorder)", "oral leukoplakia of lips (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leukoplakia of lips", "shortest_name_length": 15}
{"curie": "UMLS:C1512250", "names": ["FIGO Grade 1 Endometrial Mucinous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Grade 1 Endometrial Mucinous Adenocarcinoma", "shortest_name_length": 48}
{"curie": "MONDO:0006850", "names": ["maxillary sinus tumor", "Maxillary Sinus Tumor", "maxillary antrum tumor", "Maxillary sinus--Tumors", "Tumor of maxillary sinus", "Tumor of Maxillary Sinus", "Maxillary Sinus Neoplasm", "tumor of maxillary sinus", "maxillary sinus neoplasm", "Maxillary Sinus Neoplasms", "Neoplasm, Maxillary Sinus", "maxillary antrum neoplasm", "tumor of maxillary antrum", "maxillofacial sinus tumor", "Tumor of maxillary antrum", "Tumour of maxillary sinus", "Neoplasms, Maxillary Sinus", "Tumour of maxillary antrum", "neoplasm of maxillary sinus", "Neoplasm of maxillary sinus", "Neoplasm of Maxillary Sinus", "tumor of Maxillofacial sinus", "maxillofacial sinus neoplasm", "Tumor of the Maxillary Sinus", "tumor of maxillofacial sinus", "tumor of the maxillary sinus", "neoplasm of maxillary antrum", "Maxillofacial sinus neoplasm", "tumor of the maxillary antrum", "Maxillofacial sinuses neoplasm", "MAXILLOFACIAL SINUSES NEOPLASM", "neoplasm of maxillofacial sinus", "maxillary sinus benign neoplasm", "Neoplasm of the Maxillary Sinus", "neoplasm of the maxillary sinus", "tumor of the maxillofacial sinus", "neoplasm of the maxillary antrum", "maxillary sinus neoplasm (disease)", "neoplasm of the maxillofacial sinus", "Neoplasm of maxillary sinus (disorder)", "neoplasm of maxillary sinus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maxillary sinus neoplasm", "shortest_name_length": 21}
{"curie": "MONDO:0001225", "names": ["Opioid Abuse", "opioid abuse", "Opioid abuse", "Abuse, Opioid", "abuse opioids", "Opioid Abuses", "opioids; abuse", "abuse; opioids", "Opioid abuse (disorder)", "opioid abuse (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "opioid abuse", "shortest_name_length": 12}
{"curie": "MONDO:0024303", "names": ["external hirudiniasis", "External Hirudiniasis", "External hirudiniasis", "External hirudiniasis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "external hirudiniasis", "shortest_name_length": 21}
{"curie": "MONDO:0003770", "names": ["Thoracic Intraspinal Meningioma", "thoracic intraspinal meningioma", "thoracic spinal canal and spinal cord meningioma", "Thoracic Spinal Canal and Spinal Cord Meningioma", "meningioma of thoracic spinal canal and spinal cord", "Meningioma of Thoracic Spinal Canal and Spinal Cord", "Meningioma of the Thoracic Spinal Canal and Spinal Cord", "meningioma of the Thoracic Spinal canal and Spinal Cord", "meningioma of the thoracic spinal canal and spinal cord"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thoracic spinal canal and spinal cord meningioma", "shortest_name_length": 31}
{"curie": "MONDO:0009350", "names": ["HOLZGREVE SYNDROME", "Holzgreve syndrome", "Holzgreve syndrome (disorder)", "Holzgreve Wagner Rehder syndrome", "Holzgreve-Wagner-Rehder Syndrome", "Holzgreve Wagner Rehder Syndrome", "Holzgreve-Wagner-Rehder syndrome", "Complex congenital heart defect, renal agenesis and cleft lip and palate", "Complex congenital heart defect, renal agenesis, and cleft lip and palate", "cleft palate-Potter sequence-congenital heart anomalies-mesoaxial polydactyly-multiple malformations syndrome", "Cleft palate-Potter sequence-congenital heart anomalies-mesoaxial polydactyly-multiple malformations syndrome", "Cleft palate, Potter sequence, congenital heart anomalies, mesoaxial polydactyly, multiple malformations syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Holzgreve-Wagner-Rehder syndrome", "shortest_name_length": 18}
{"curie": "UMLS:C0573209", "names": ["Beta-blocker overdose", "beta-blocker overdose", "beta blocker overdose", "beta blockers overdose", "Overdose of beta-adrenergic blocking drug", "Overdose of beta-adrenergic blocking drug (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Overdose of beta-adrenergic blocking drug", "shortest_name_length": 21}
{"curie": "MONDO:0011349", "names": ["Osteoma of Cranial Vault, Familial", "osteoma of cranial vault, familial", "OSTEOMA OF CRANIAL VAULT, FAMILIAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteoma of cranial vault, familial", "shortest_name_length": 34}
{"curie": "UMLS:C4285693", "names": ["HIV-associated neurocognitive disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HIV-associated neurocognitive disorder", "shortest_name_length": 38}
{"curie": "UMLS:C0854802", "names": ["relapsed CLL", "CLL, relapsed", "Relapsed Chronic Lymphoid Leukemia", "Recurrent Chronic Lymphoid Leukemia", "Chronic lymphoid leukemia in relapse", "Chronic lymphoid leukemia, in relapse", "Relapsed Chronic Lymphocytic Leukemia", "relapsed chronic lymphocytic leukemia", "chronic lymphocytic leukemia, relapsed", "leukemia, relapsed chronic lymphocytic", "Chronic lymphocytic leukemia recurrent", "Chronic Lymphocytic Leukemia Recurrent", "lymphocytic leukemia, relapsed chronic", "Recurrent Chronic Lymphocytic Leukemia", "chronic lymphocytic leukemia in relapse", "Chronic lymphocytic leukaemia recurrent", "Recurrent Chronic Lymphocytic Leukemia (CLL)", "CLL (chronic lymphocytic leukemia) in relapse", "Recurrent B-Cell Chronic Lymphocytic Leukemia", "Chronic lymphoid leukemia in relapse (disorder)", "chronic lymphocytic leukemia in relapse (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Chronic Lymphoid Leukemia", "shortest_name_length": 12}
{"curie": "MONDO:0054743", "names": ["PCLD3", "POLYCYSTIC LIVER DISEASE 3 WITH OR WITHOUT KIDNEY CYSTS", "polycystic liver disease 3 with or without kidney cysts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polycystic liver disease 3 with or without kidney cysts", "shortest_name_length": 5}
{"curie": "MONDO:0015742", "names": ["PVL", "White matter necrosis", "leukomalacia periventricular", "periventricular leukomalacia", "Periventricular leucomalacia", "Periventricular Leukomalacia", "periventricular leucomalacia", "Periventricular Leucomalacia", "Periventricular leukomalacia", "Leucomalacia, Periventricular", "Periventricular Leucomalacias", "Leukomalacia, Periventricular", "Periventricular Leukomalacias", "Leucomalacias, Periventricular", "Leukomalacias, Periventricular", "pvl leukomalacia periventricular", "Periventricular Encephalomalacia", "Encephalomalacia, Periventricular", "Periventricular Encephalomalacias", "Encephalomalacias, Periventricular", "PVL - Periventricular leukomalacia", "PVL - Periventricular leucomalacia", "Periventricular leukoencephalopathy", "Periventricular leucoencephalopathy", "Leukoencephalopathy, periventricular", "Periventricular leukomalacia (disorder)", "periventricular leukomalacia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "periventricular leukomalacia", "shortest_name_length": 3}
{"curie": "UMLS:C5206436", "names": ["Stage IA Cervical Cancer FIGO 2018", "Stage IA Cervical Carcinoma FIGO 2018"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Cervical Cancer FIGO 2018", "shortest_name_length": 34}
{"curie": "MONDO:0006435", "names": ["submandibular gland adenocarcinoma", "Submandibular Gland Adenocarcinoma", "adenocarcinoma of submandibular gland", "Adenocarcinoma of Submandibular Gland", "Adenocarcinoma of the Submandibular Gland", "adenocarcinoma of the submandibular gland", "adenocarcinoma of submandibular gland (diagnosis)", "malignant salivary gland neoplasm submandibular adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "submandibular gland adenocarcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0021183", "names": ["INFECT HTLV II", "HTLV II INFECT", "HTLV-2 infection", "HTLV-II Infection", "HTLV-II infection", "HTLV-II Infections", "Infection, HTLV-II", "Infections, HTLV-II", "Infections, HTLV II", "Human T-lymphotropic virus 2 infection", "Human T lymphotropic Virus 2 Infection", "Human T-lymphotropic Virus 2 Infection", "Human T lymphotropic Virus 2 Infections", "Human T-lymphotropic Virus 2 Infections", "Human T-lymphotropic virus 2 infectious disease", "human T-lymphotropic virus 2 (HTLV-II) infection", "Human T-lymphotropic virus 2 infection (disorder)", "human T-lymphotropic virus 2 (HTLV-II) infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HTLV-2 infection", "shortest_name_length": 14}
{"curie": "MONDO:0600017", "names": ["FGF10 acinar dysplasia", "FGF10 related acinar dysplasia", "acinar dysplasia caused by mutation in FGF10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acinar dysplasia caused by mutation in FGF10", "shortest_name_length": 22}
{"curie": "UMLS:C0558595", "names": ["Uric acid renal calculus", "Uric acid nephrolithiasis", "Uric acid renal calculus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uric acid renal calculus", "shortest_name_length": 24}
{"curie": "MONDO:0001723", "names": ["progressive peripheral pterygium", "Progressive peripheral pterygium", "Peripheral pterygium, progressive", "Peripheral pterygium, progressive (disorder)", "progressive peripheral pterygium (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive peripheral pterygium", "shortest_name_length": 32}
{"curie": "UMLS:C1112480", "names": ["Mediastinal bleeding", "Mediastinal Hemorrhage", "Mediastinal hemorrhage", "Mediastinal haemorrhage", "Hemorrhage of mediastinum", "Hemorrhage of mediastinum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mediastinal Hemorrhage", "shortest_name_length": 20}
{"curie": "MONDO:0016991", "names": ["ANEC", "isolated ANE", "Isolated ANE", "Isolated acute necrotising encephalopathy", "isolated acute necrotizing encephalopathy", "Isolated acute necrotizing encephalopathy", "acute necrotizing encephalopathy of childhood", "Acute necrotizing encephalopathy of childhood", "Acute necrotising encephalopathy of childhood", "Acute necrotizing encephalopathy of childhood (disorder)", "acute necrotizing encephalopathy of childhood (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute necrotizing encephalopathy of childhood", "shortest_name_length": 4}
{"curie": "MONDO:0054666", "names": ["ODG5", "ovarian dysgenesis 5", "OVARIAN DYSGENESIS 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian dysgenesis 5", "shortest_name_length": 4}
{"curie": "MONDO:0018911", "names": ["MODY", "mody", "modi", "NIDDY", "Mason-Type Diabetes", "MASON-TYPE DIABETES", "Mason-type diabetes", "Mason type diabetes", "diabetes maturity onset young", "diabetes maturity onset youth", "maturity onset diabetes in youth", "Maturity onset diabetes in youth", "Maturity Onset Diabetes of the Young", "MATURITY-ONSET DIABETES OF THE YOUNG", "Maturity onset diabetes of the young", "maturity onset diabetes of the young", "Maturity-onset diabetes of the young", "maturity-onset diabetes of the young", "Maturity-Onset Diabetes of the Young", "Diabetes mellitus autosomal dominant", "Autosomal dominant diabetes mellitus", "MODY - maturity onset diabetes of young", "Maturity onset diabetes mellitus in young", "Maturity-onset diabetes of the young (MODY)", "Diabetes, maturity-onset, of the young (MODY)", "MODY - Maturity onset diabetes in youth type I", "MODY - Maturity onset diabetes in youth type 1", "maturity-onset diabetes of the young (disease)", "Maturity-onset diabetes of the young (disorder)", "maturity-onset diabetes of the young (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maturity-onset diabetes of the young", "shortest_name_length": 4}
{"curie": "UMLS:C2931105", "names": ["Childhood idiopathic hypercalciuria", "Hypercalciuria, childhood idiopathic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypercalciuria, childhood idiopathic", "shortest_name_length": 35}
{"curie": "MONDO:0014036", "names": ["AD17", "Alzheimer Disease 17", "ALZHEIMER DISEASE 17", "Alzheimer disease 17", "Alzheimer's Disease 17", "Alzheimer's disease 17", "Alzheimer's disease type 17", "Alzheimer disease 17, late-onset", "ALZHEIMER DISEASE 17, LATE-ONSET", "Alzheimer disease 17, late onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alzheimer disease 17", "shortest_name_length": 4}
{"curie": "UMLS:C1336172", "names": ["Stage IIA Small Cell Lung Cancer", "Stage IIA Small Cell Lung Carcinoma", "Stage IIA Small Cell Carcinoma of Lung", "Stage IIA Small Cell Carcinoma of the Lung", "Stage IIA Lung Small Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Lung Small Cell Carcinoma AJCC v7", "shortest_name_length": 32}
{"curie": "MONDO:0032650", "names": ["CONDCA", "NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATROPHY", "neurodegeneration, childhood-onset, with cerebellar atrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodegeneration, childhood-onset, with cerebellar atrophy", "shortest_name_length": 6}
{"curie": "UMLS:C0161026", "names": ["Penile FB", "foreign body; penis", "penis; foreign body", "Foreign Body in Penis", "foreign body of penis", "Foreign body in penis", "Foreign body in penis (disorder)", "foreign body of penis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Foreign body in penis", "shortest_name_length": 9}
{"curie": "MONDO:0007792", "names": ["FBH2", "HHC2", "FHH type 2", "hpocalciuric hypercalcemia, type II", "hypocalciuric hypercalcemia type II", "familial benign hypercalcemia, type 2", "hypercalcemia, familial benign type 2", "Hypercalcemia, familial benign type 2", "Familial benign hypercalcemia, type 2", "FAMILIAL BENIGN HYPERCALCEMIA, TYPE II", "familial hypocalciuric hypercalcemia 2", "hypercalcemia, familial benign, type 2", "Familial Benign Hypercalcemia, Type II", "Hypercalcemia, Familial Benign, Type II", "HYPERCALCEMIA, FAMILIAL BENIGN, TYPE II", "familial hypocalciuric hypercalcemia type 2", "Familial hypocalciuric hypercalcemia type 2", "familial hypocalciuric hypercalcemia type II", "hypocalciuric hypercalcemia, familial, type 2", "Hypocalciuric hypercalcemia, familial, type 2", "HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE II", "hypocalciuric hypercalcemia, familial, type II", "Hypocalciuric Hypercalcemia, Familial, Type II", "familial hypocalciuric hypercalcemia type II (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial hypocalciuric hypercalcemia 2", "shortest_name_length": 4}
{"curie": "MONDO:0017760", "names": ["disorder of other vitamins and cofactors metabolism and transport"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of other vitamins and cofactors metabolism and transport", "shortest_name_length": 65}
{"curie": "MONDO:0008192", "names": ["PGL", "PGL1", "CHEMODECTOMA", "Chemodectoma", "chemodectoma", "Chemodectomas", "chemodectomas", "Paragangliomata", "PARAGANGLIOMATA", "Paragangliomas 1", "PARAGANGLIOMAS 1", "Heart base tumor", "paragangliomas 1", "Heart base tumour", "SDHD paraganglioma", "carotid body tumors", "paragangliomas type 1", "Chemodectoma syndrome", "glomus jugulare tumors", "Extraadrenal Paraganglioma", "glomus tumors, familial, 1", "Glomus Tumors, Familial, 1", "GLOMUS TUMORS, FAMILIAL, 1", "Extra-adrenal paraganglioma", "Extra-Adrenal Paraganglioma", "paragangliomas, familial, 1", "Paragangliomas, Familial, 1", "Nonchromaffin paraganglioma", "PARAGANGLIOMAS, FAMILIAL, 1", "Nonchromaffin Paraganglioma", "extra-adrenal paraganglioma", "paraganglioma, carotid body", "Nonchromaffin Paragangliomas", "PARAGANGLIOMA, NONCHROMAFFIN", "Paraganglioma, Extra Adrenal", "Non-Chromaffin Paraganglioma", "Paraganglioma, Extra-Adrenal", "Paraganglioma, Nonchromaffin", "Extra-Adrenal Paragangliomas", "Non-chromaffin paraganglioma", "Paraganglioma, Non-Chromaffin", "Non-Chromaffin Paragangliomas", "Paragangliomas, Extra-Adrenal", "Paraganglioma, Non Chromaffin", "Paragangliomas, Nonchromaffin", "Paragangliomas, Non-Chromaffin", "Extra-adrenal paraganglioma NOS", "Extra-adrenal paraganglioma, NOS", "Nonchromaffin paraganglioma, NOS", "[M]Extra-adrenal paraganglioma, NOS", "Extra-Adrenal Paraganglionic Neoplasm", "Extra-adrenal paraganglioma (disorder)", "extra-adrenal paraganglioma (diagnosis)", "neoplasm of paraganglioma extra-adrenal", "paraganglioma caused by mutation in SDHD", "Paragangliomas, Familial Nonchromaffin, 1", "paragangliomas, familial nonchromaffin, 1", "PARAGANGLIOMAS, FAMILIAL NONCHROMAFFIN, 1", "paragangliomas 1, with or without deafness", "PARAGANGLIOMAS WITH SENSORINEURAL HEARING LOSS", "Paragangliomas with Sensorineural Hearing Loss", "paragangliomas with sensorineural hearing loss", "Extra-adrenal paraganglioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paragangliomas 1", "shortest_name_length": 3}
{"curie": "UMLS:C5556677", "names": ["Cervical Mucinous Adenocarcinoma, NOS", "Cervical Mucinous Adenocarcinoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Mucinous Adenocarcinoma, Not Otherwise Specified", "shortest_name_length": 37}
{"curie": "UMLS:C1510475", "names": ["diverticulosis", "Diverticulosis", "DIVERTICULOSIS", "ENTERIC DIVERTICULUM", "Diverticular disease", "Diverticular Disorder", "Diverticular disorders", "diverticulum intestinal", "intestinal diverticulum", "Diverticulum intestinal", "Diverticula of intestine", "DD - Diverticular disease", "diverticulosis (diagnosis)", "Diverticulosis of intestine", "Diverticula of intestine, NOS", "intestinal disorder diverticular", "Diverticular disease of intestine", "Multiple diverticula of intestine", "Multiple diverticula of intestine (finding)", "Diverticular disease of intestine (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diverticulosis", "shortest_name_length": 14}
{"curie": "UMLS:C5447695", "names": ["Angiofibroma of Soft Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Angiofibroma of Soft Tissue", "shortest_name_length": 27}
{"curie": "UMLS:C2828011", "names": ["Stage IA Merkel Cell Carcinoma", "Stage IA Merkel Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Merkel Cell Carcinoma AJCC v7", "shortest_name_length": 30}
{"curie": "UMLS:C5205651", "names": ["Recurrent Anaplastic Ependymoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Anaplastic Ependymoma", "shortest_name_length": 31}
{"curie": "UMLS:C0860239", "names": ["catheter related infection", "Catheter-Related Infection", "Catheter related infection", "Catheter Related Infection", "Infection, Catheter Related", "Catheter-Related Infections", "Catheter Related Infections", "Infection, Catheter-Related", "Related Infection, Catheter", "catheter infections related", "Related Infections, Catheter", "Infections, Catheter-Related", "Infections, Catheter Related", "Catheter Associated Infection", "Catheter-Associated Infection", "Catheter Associated Infections", "Infection, Catheter-Associated", "Catheter-Associated Infections", "Associated Infection, Catheter", "Infection, Catheter Associated", "Infections, Catheter Associated", "Associated Infections, Catheter", "Infections, Catheter-Associated", "Infection associated with catheter", "Infection associated with catheter (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Catheter related infection", "shortest_name_length": 26}
{"curie": "MONDO:0013583", "names": ["OCCM", "occipital MCD", "cortical malformations, occipital", "CORTICAL MALFORMATIONS, OCCIPITAL", "occipital pachygyria and polymicrogyria", "occipital malformations of cortical development"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "occipital pachygyria and polymicrogyria", "shortest_name_length": 4}
{"curie": "MONDO:0024621", "names": ["serous adenocarcinoma", "Serous Adenocarcinoma", "Serous Cystadenocarcinoma", "serous cystadenocarcinoma", "Serous adenocarcinoma, NOS", "Serous cystadenocarcinoma, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "serous cystadenocarcinoma", "shortest_name_length": 21}
{"curie": "MONDO:0003650", "names": ["mixed hepatoblastoma", "Mixed epithelial-mesenchymal hepatoblastoma", "Hepatoblastoma, mixed epithelial-mesenchymal", "Mixed Epithelial and Mesenchymal Hepatoblastoma", "mixed epithelial and mesenchymal hepatoblastoma", "Mixed epithelial-mesenchymal hepatoblastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed hepatoblastoma", "shortest_name_length": 20}
{"curie": "MONDO:0018857", "names": ["creeping myiasis", "Creeping myiasis", "Migratory myiasis", "migratory myiasis", "Myiasitic creeping eruption", "Creeping myiasis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "creeping myiasis", "shortest_name_length": 16}
{"curie": "UMLS:C4526962", "names": ["GIST by AJCC v8 Stage", "Gastrointestinal Stromal Tumor by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal Stromal Tumor by AJCC v8 Stage", "shortest_name_length": 21}
{"curie": "MONDO:0007158", "names": ["DA5", "DAIIB", "oculomelic amyoplasia", "Oculomelic amyoplasia", "OCULOMELIC AMYOPLASIA", "Distal arthrogryposis type 5", "distal arthrogryposis type 5", "distal type 5 arthrogryposis", "arthrogryposis distal type 5", "Arthrogryposis, Distal, Type 5", "arthrogryposis, distal, type 5", "ARTHROGRYPOSIS, DISTAL, TYPE 5", "distal arthrogryposis type IIB", "Distal arthrogryposis type IIB", "arthrogryposis, distal, type 2B", "Arthrogryposis, Distal, Type IIb", "ARTHROGRYPOSIS, DISTAL, TYPE IIB", "Distal arthrogryposis type 5 (disorder)", "distal type 5 arthrogryposis (diagnosis)", "distal arthrogryposis with ophthalmoplegia", "Distal arthrogryposis with ophthalmoplegia", "arthrogryposis ophthalmoplegia retinopathy", "Arthrogryposis with oculomotor limitation and electroretinal anomaly", "Arthrogryposis-oculomotor limitation-electroretinal anomalies syndrome", "arthrogryposis-oculomotor limitation-electroretinal anomalies syndrome", "arthrogryposis- oculomotor limitation-electroretinal anomalies syndrome", "Arthogryposis with oculomotor limitation and electroretinal abnormalities", "arthrogryposis with oculomotor limitation and electroretinal abnormalities", "ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES", "Arthrogryposis with oculomotor limitation and electroretinal abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis- oculomotor limitation-electroretinal anomalies syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0022739", "names": ["Christian demyer franken syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Christian demyer franken syndrome", "shortest_name_length": 33}
{"curie": "MONDO:0011365", "names": ["YSS", "SBBYSS", "SBBYSS syndrome", "Young Simpson syndrome", "YOUNG-SIMPSON SYNDROME", "Young-Simpson syndrome", "Young-Simpson Syndrome", "Ohdo syndrome, SBBYS variant", "Ohdo Syndrome, SBBYS Variant", "Ohdo syndrome, SBBYS Variant", "OHDO SYNDROME, SBBYS VARIANT", "SBBYS Variant of Ohdo Syndrome", "SBBYS variant of Ohdo syndrome", "SAY-BARBER-BIESECKER-YOUNG-SIMPSON SYNDROME", "Say-Barber-Biesecker-Young-Simpson syndrome", "Ohdo Syndrome, Say-Barber-Biesecker Variant", "Say-Barber-Biesecker-Young-Simpson Syndrome", "Mental retardation unusual facies hypothyroidism", "Ohdo Syndrome, Say-Barber-Biesecker-Young-Simpson Variant", "Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant", "Say-Barber-Biesecker-Young-Simpson Variant of Ohdo Syndrome", "Say-Barber-Biesecker-Young-Simpson variant of Ohdo syndrome", "Blepharophimosis-intellectual disability syndrome, SBBYS type", "blepharophimosis-intellectual disability syndrome, SBBYS type", "blepharophimosis - intellectual disability syndrome, SBBYS type", "hypothyroidism-dysmorphism-postaxial polydactyly-intellectual disability syndrome", "Hypothyroidism-dysmorphism-postaxial polydactyly-intellectual disability syndrome", "Hypothyroidism, dysmorphism, postaxial polydactyly, intellectual disability syndrome", "Blepharophimosis-intellectual deficit syndrome, Say-Barber/Biesecker/Young-Simpson type", "Blepharophimosis-Intellectual Deficit Syndrome, Say-Barber-Biesecker-Young-Simpson Type", "Blepharophimosis and Mental Retardation Syndrome, Say-Barber-Biesecker-Young-Simpson Type", "Blepharophimosis, intellectual disability syndrome, Say-Barber-Biesecker-Young-Simpson type", "blepharophimosis and intellectual disability syndrome, Say-Barber-Biesecker-Young-Simpson type", "Blepharophimosis, intellectual disability syndrome, Say-Barber-Biesecker-Young-Simpson type (disorder)", "blepharophimosis and intellectual disability syndrome, Say-Barber-Biesecker-Young-Simpson type (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blepharophimosis - intellectual disability syndrome, SBBYS type", "shortest_name_length": 3}
{"curie": "MONDO:0016669", "names": ["HbSC", "Hb-SC", "SC Disease", "sc disease", "SC Diseases", "Disease, SC", "HbSC disease", "Diseases, SC", "hemoglobin sc", "Hb-SC disease", "Hb SC-disease", "HEMOGLOBIN SC", "Hb SC disease", "HbS-HbC disease", "hemoglobin; Hb-SC", "Hb-S/Hb-C disease", "sickle-cell; Hb-SC", "Hb-SC; sickle-cell", "Hemoglobin SC disease", "HEMOGLOBIN SC DISEASE", "Hemoglobin SC Disease", "hemoglobin sc disease", "hemoglobin s c disease", "Disease, Hemoglobin SC", "hemoglobin s-c disease", "SC Disease, Hemoglobin", "Hemoglobin SC Diseases", "Hemoglobin S-C disease", "Haemoglobin SC disease", "Hemoglobin S/C disease", "Haemoglobin S/C disease", "SC Diseases, Hemoglobin", "Diseases, Hemoglobin SC", "Haemoglobin S-C disease", "Sickle cell hemoglobin C", "Sickle-cell/Hb-C disease", "Sickle cell Hb-C disease", "Sickle cell haemoglobin C", "sickle cell-hemoglobin c disease", "Sickle Cell Hemoglobin C Disease", "sickle cell-hemoglobin C disease", "Sickle cell-hemoglobin C disease", "SICKLE CELL-HEMOGLOBIN C DISEASE", "Sickle Cell-Hemoglobin C Disease", "Sickle cell-haemoglobin C disease", "sickle cell - hemoglobin C disease", "Double heterozygous for Hb S and Hb D", "sickle cell Hb-C disease without crisis", "Sickle-cell/Hb-C disease without crisis", "sickle cell-hemoglobin c disease syndrome", "Sickle cell-hemoglobin C disease syndrome", "anemia hemolytic sickle cell/Hb-C disease", "Sickle cell-hemoglobin C disease (disorder)", "disease (or disorder); hemoglobin or Hb, SC", "Sickle cell anemia with hemoglobin C disease", "sickle cell-hemoglobin C disease (diagnosis)", "Sickle cell anaemia with haemoglobin C disease", "sickle cell Hb-C disease without crisis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sickle cell-hemoglobin c disease syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0033116", "names": ["SCAR26", "autosomal recessive spinocerebellar ataxia 26", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 26", "spinocerebellar ataxia, autosomal recessive 26"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia, autosomal recessive 26", "shortest_name_length": 6}
{"curie": "UMLS:C1334746", "names": ["Methotrexate-Associated Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Methotrexate-Associated Diffuse Large B-Cell Lymphoma", "shortest_name_length": 53}
{"curie": "MONDO:0009031", "names": ["CDD", "Lionitis", "Craniodiaphyseal Dysplasia", "Craniodiaphyseal dysplasia", "CRANIODIAPHYSEAL DYSPLASIA", "craniodiaphyseal dysplasia", "CDD - Craniodiaphyseal dysplasia", "Craniodiaphyseal dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniodiaphyseal dysplasia", "shortest_name_length": 3}
{"curie": "UMLS:C0853954", "names": ["Corneal calcification"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Corneal calcification", "shortest_name_length": 21}
{"curie": "MONDO:0004429", "names": ["skin meningioma", "Primary Skin Meningioma", "Primary Meningioma of Skin", "Primary Cutaneous Meningioma", "Primary Meningioma of the Skin", "primary meningioma of the skin", "zone of skin meningioma (disease)", "meningioma (disease) of zone of skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin meningioma", "shortest_name_length": 15}
{"curie": "UMLS:C0085222", "names": ["PSOAS ABSCESS", "psoas abscess", "Psoas Abscess", "Psoas abscess", "psoas; abscess", "Abscess, Psoas", "Psoas Abscesses", "psoas abscesses", "Abscesses, Psoas", "Iliopsoas abscess", "Iliopsoas Abscess", "iliopsoas abscess", "Abscess, Iliopsoas", "Iliopsoas Abscesses", "Psoas muscle abscess", "psoas muscle abscess", "Abscesses, Iliopsoas", "PSOAS MUSCLE ABSCESS", "psoas abscess (diagnosis)", "Pyogenic Iliopsoas Abscess", "Abscess, Pyogenic Iliopsoas", "Iliopsoas Abscess, Pyogenic", "Iliopsoas abscess (disorder)", "Pyogenic Iliopsoas Abscesses", "Iliopsoas Abscesses, Pyogenic", "Abscesses, Pyogenic Iliopsoas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Psoas Abscess", "shortest_name_length": 13}
{"curie": "MONDO:0007838", "names": ["JBS", "monosomy 11q", "11q- syndrome", "Del(11)(qter)", "Del(11)(q23.3)", "Monosomy 11qter", "monosomy 11qter", "Jacobsen Syndrome", "Jacobsen syndrome", "del(11q) syndrome", "jacobsen syndrome", "JACOBSEN SYNDROME", "Distal deletion 11q", "distal monosomy 11q", "distal deletion 11q", "Distal monosomy 11q", "partial monosomy 11q", "11q Deletion Syndrome", "deletion 11q syndrome", "11q deletion syndrome", "11q Deletion Disorder", "telomeric deletion 11q", "Telomeric deletion 11q", "Deletion Disorder, 11q", "11q- Deletion Syndrome", "11q- Deletion Syndromes", "Deletion Syndrome, 11q-", "Jacobsen syndrome (JBS)", "chromosome 11q monosomy", "Partial 11q Monosomy Syndrome", "PARTIAL 11q MONOSOMY SYNDROME", "11q partial monosomy syndrome", "Jacobsen syndrome (diagnosis)", "partial 11q monosomy syndrome", "11q Terminal Deletion Disorder", "11q terminal deletion disorder", "11q terminal deletion syndrome", "CHROMOSOME 11q DELETION SYNDROME", "chromosome 11q deletion syndrome", "Chromosome 11q Deletion Syndrome", "Jacobsen syndrome, Isolated cases", "Jacobsen Distal 11q Deletion Syndrome", "Jacobsen distal 11q deletion syndrome", "11q partial monosomy syndrome (disorder)", "11q partial monosomy syndrome (diagnosis)", "Distal partial deletion of long arm of chromosome 11", "anomaly of chromosome pair 11q partial monosomy syndrome", "Distal partial deletion of long arm of chromosome 11 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jacobsen syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C4521711", "names": ["IIIB", "Stage IIIB Esophageal Adenocarcinoma", "Pathologic Stage IIIB Esophageal Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IIIB Esophageal Adenocarcinoma AJCC v8", "shortest_name_length": 4}
{"curie": "MONDO:0004405", "names": ["Barrett Adenocarcinoma", "Barrett adenocarcinoma", "Barrett's Adenocarcinoma", "Barrett's adenocarcinoma", "Primary Barrett adenocarcinoma", "adenocarcinoma Arising in Barrett's Mucosa", "adenocarcinoma arising in Barrett's mucosa", "Adenocarcinoma Arising in Barrett's Mucosa", "Primary adenocarcinoma of lower third of esophagus due to Barrett esophagus", "Primary adenocarcinoma of lower third of oesophagus due to Barrett oesophagus", "Primary adenocarcinoma of lower third of esophagus due to Barrett esophagus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Barrett adenocarcinoma", "shortest_name_length": 22}
{"curie": "UMLS:C5557152", "names": ["Stage IA1 Cervical Cancer AJCC v9", "Stage IA1 Cervical Carcinoma AJCC v9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA1 Cervical Cancer AJCC v9", "shortest_name_length": 33}
{"curie": "UMLS:C0406806", "names": ["Moniliform hamartoma", "Moniliform Hamartoma", "Hamartoma Moniliformis", "Hamartoma moniliformis", "Moniliform hamartoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Moniliform hamartoma", "shortest_name_length": 20}
{"curie": "MONDO:0008615", "names": ["DYSMELODIA", "Dysmelodia", "Tone deafness", "TUNE DEAFNESS", "tune deafness", "tone deafness", "TONE DEAFNESS", "Tune Deafness", "Sensory amusia", "Deafness, tone", "amusia, congenital", "Amusia, Congenital", "AMUSIA, CONGENITAL", "tone deafness (symptom)", "Tone deafness (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tune deafness", "shortest_name_length": 10}
{"curie": "UMLS:C4521823", "names": ["IVA", "Stage IVA Hilar Cholangiocarcinoma", "Stage IVA Hilar Cholangiocarcinoma AJCC v8", "Stage IVA Perihilar Cholangiocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Hilar Cholangiocarcinoma AJCC v8", "shortest_name_length": 3}
{"curie": "MONDO:0009518", "names": ["LPRS3", "TLR2 leprosy", "leprosy, susceptibility to", "susceptibility to leprosy 3", "LEPROSY, SUSCEPTIBILITY TO, 3", "leprosy, susceptibility to, 3", "leprosy, susceptibility to, type 3", "leprosy caused by mutation in TLR2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leprosy, susceptibility to, 3", "shortest_name_length": 5}
{"curie": "UMLS:C4721795", "names": ["Stage IIIB Ovarian Cancer", "Ovarian Cancer Stage IIIB", "AJCC Stage IIIB Ovarian Cancer", "FIGO Stage IIIB Ovarian Cancer", "FIGO Stage IIIB Cancer of Ovary", "Stage IIIB Ovarian Cancer AJCC v6", "FIGO Stage IIIB Ovarian Carcinoma", "Stage IIIB Ovarian Cancer AJCC v7", "FIGO Stage IIIB Carcinoma of Ovary", "FIGO Stage IIIB Cancer of the Ovary", "Stage IIIB Ovarian Epithelial Cancer", "FIGO Stage IIIB Carcinoma of the Ovary", "Stage IIIB Ovarian Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Ovarian Cancer AJCC v6 and v7", "shortest_name_length": 25}
{"curie": "MONDO:0012196", "names": ["AUNA1", "NSDAN", "DIAPH3 auditory neuropathy", "autosomal dominant auditory neuropathy 1", "AUDITORY NEUROPATHY, AUTOSOMAL DOMINANT 1", "nonsyndromic dominant auditory neuropathy", "Auditory Neuropathy, Autosomal Dominant, 1", "AUDITORY NEUROPATHY, NONSYNDROMIC DOMINANT", "Auditory Neuropathy, Nonsyndromic Dominant", "AUDITORY NEUROPATHY, AUTOSOMAL DOMINANT, 1", "auditory neuropathy, nonsyndromic dominant", "auditory neuropathy, autosomal dominant, 1", "autosomal dominant auditory neuropathy type 1", "auditory neuropathy, autosomal dominant, type 1", "auditory neuropathy caused by mutation in DIAPH3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant auditory neuropathy 1", "shortest_name_length": 5}
{"curie": "UMLS:C4288763", "names": ["Membranous Nephropathy - Secondary", "Secondary Membranous Glomerulopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Membranous Nephropathy - Secondary", "shortest_name_length": 34}
{"curie": "UMLS:C0695236", "names": ["Tracheostomy infection", "Infection of tracheostomy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tracheostomy infection", "shortest_name_length": 22}
{"curie": "UMLS:C0919894", "names": ["Nasal mucosal disorder", "Nasal mucosal disorder NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasal mucosal disorder", "shortest_name_length": 22}
{"curie": "UMLS:C1619702", "names": ["Device-Related Infection", "Device related infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Device related infection", "shortest_name_length": 24}
{"curie": "MONDO:0014303", "names": ["SPG64", "hereditary spastic paraplegia 64", "hereditary spastic paraplegia type 64", "autosomal recessive spastic paraplegia 64", "spastic paraplegia 64, autosomal recessive", "SPASTIC PARAPLEGIA 64, AUTOSOMAL RECESSIVE", "autosomal recessive spastic paraplegia type 64", "Autosomal recessive spastic paraplegia type 64", "ENTPD1 autosomal recessive complex spastic paraplegia", "familial spastic paraplegia autosomal recessive type 64", "Autosomal recessive spastic paraplegia type 64 (disorder)", "Autosomal recessive spastic paraplegia type 64 (diagnosis)", "autosomal recessive complex spastic paraplegia caused by mutation in ENTPD1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 64", "shortest_name_length": 5}
{"curie": "MONDO:0014084", "names": ["AOA3", "ATAXIA-OCULOMOTOR APRAXIA 3", "ataxia-oculomotor apraxia-3", "ataxia-oculomotor apraxia 3", "ataxia-oculomotor apraxia type 3", "Ataxia-Oculomotor Apraxia Type 3", "ataxia with oculomotor apraxia type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ataxia with oculomotor apraxia type 3", "shortest_name_length": 4}
{"curie": "UMLS:C5238522", "names": ["Advanced Primary Peritoneal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Primary Peritoneal Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0100388", "names": ["AML, Monosomy 5", "acute myeloid leukemia, Monosomy 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, Monosomy 5", "shortest_name_length": 15}
{"curie": "MONDO:0017831", "names": ["mild Canavan disease", "juvenile Canavan disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mild Canavan disease", "shortest_name_length": 20}
{"curie": "MONDO:0017818", "names": ["lethal arteriopathy syndrome due to fibulin-4 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal arteriopathy syndrome due to fibulin-4 deficiency", "shortest_name_length": 56}
{"curie": "UMLS:C5236017", "names": ["FH-Deficient RCC", "FH-Deficient Renal Cell Carcinoma", "Fumarate Hydratase-Deficient Renal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fumarate Hydratase-Deficient Renal Cell Carcinoma", "shortest_name_length": 16}
{"curie": "UMLS:C2987189", "names": ["ITPN", "Pancreatic ITPN", "Pancreatic Intraductal Tubular Neoplasm", "Pancreatic Intraductal Tubulopapillary Neoplasm", "Intraductal tubulopapillary neoplasm of pancreas", "Intraductal Tubulopapillary Neoplasm, Pancreatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Intraductal Tubulopapillary Neoplasm", "shortest_name_length": 4}
{"curie": "MONDO:0800182", "names": ["TEK-related primary glaucoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "TEK-related primary glaucoma", "shortest_name_length": 28}
{"curie": "UMLS:C0278993", "names": ["Relapsed Salivary Gland Cancer", "Salivary gland cancer recurrent", "recurrent salivary gland cancer", "Recurrent Salivary Gland Cancer", "salivary gland cancer, recurrent", "Salivary Gland Cancer, Recurrent", "Relapsed Cancer of Salivary Gland", "Relapsed Salivary Gland Carcinoma", "Recurrent Salivary Gland Carcinoma", "Recurrent Cancer of Salivary Gland", "Relapsed Carcinoma of Salivary Gland", "Relapsed Cancer of the Salivary Gland", "Recurrent Carcinoma of Salivary Gland", "Recurrent Cancer of the Salivary Gland", "Relapsed Carcinoma of the Salivary Gland", "Malignant salivary gland cancer recurrent", "Recurrent Carcinoma of the Salivary Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Salivary Gland Cancer", "shortest_name_length": 30}
{"curie": "UMLS:C4524631", "names": ["Esophageal Cancer by AJCC v8 Stage", "Esophageal Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Cancer by AJCC v8 Stage", "shortest_name_length": 34}
{"curie": "UMLS:C1333802", "names": ["Digestive Stromal Tumor", "Digestive Stromal Neoplasm", "Digestive Tract Stromal Tumor", "Stromal Tumor of Digestive Tract", "Digestive Tract Stromal Neoplasm", "Stromal Neoplasm of Digestive Tract", "Stromal Tumor of the Digestive Tract", "Gastrointestinal Tract Stromal Tumor", "Stromal Tumor of Gastrointestinal Tract", "Gastrointestinal Tract Stromal Neoplasm", "Stromal Neoplasm of the Digestive Tract", "Stromal Neoplasm of Gastrointestinal Tract", "Stromal Tumor of the Gastrointestinal Tract", "Stromal Neoplasm of the Gastrointestinal Tract", "Gastrointestinal Stromal Tumor of Gastrointestinal Tract", "Gastrointestinal Stromal Tumor of the Gastrointestinal Tract", "Gastrointestinal Stromal Tumor (GIST) of the Gastrointestinal Tract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal Stromal Tumor of the Gastrointestinal Tract", "shortest_name_length": 23}
{"curie": "UMLS:C5555763", "names": ["Hilar Cell Hyperplasia", "Ovarian Leydig Cell Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Leydig Cell Hyperplasia", "shortest_name_length": 22}
{"curie": "UMLS:C4528666", "names": ["Stage II Colorectal Cancer AJCC v8", "Stage II Colorectal Carcinoma AJCC v8", "Stage II Colorectal (Colon or Rectal) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Colorectal Cancer AJCC v8", "shortest_name_length": 34}
{"curie": "UMLS:C0855191", "names": ["Stage IV Bladder Squamous Cell Cancer", "Squamous cell bladder carcinoma stage IV", "Stage IV Bladder Squamous Cell Carcinoma", "Bladder squamous cell carcinoma stage IV", "Squamous cell carcinoma of the bladder stage IV", "Stage IV Bladder Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder squamous cell carcinoma stage IV", "shortest_name_length": 37}
{"curie": "MONDO:0014534", "names": ["LIS6", "lissencephaly 6", "KATNB1 microlissencephaly", "KATNB1 Microlissencephaly", "lissencephaly 6 with microcephaly", "LISSENCEPHALY 6 WITH MICROCEPHALY", "lissencephaly 6, with microcephaly", "Microlissencephaly caused by mutation in KATNB1", "microlissencephaly caused by mutation in KATNB1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lissencephaly 6 with microcephaly", "shortest_name_length": 4}
{"curie": "MONDO:0007242", "names": ["BUTYRYLESTERASE 1", "butyrylesterase 1", "Butyrylesterase type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "butyrylesterase 1", "shortest_name_length": 17}
{"curie": "UMLS:C0278750", "names": ["Relapsed GI Carcinoid Tumor", "Recurrent GI Carcinoid Tumor", "Relapsed Digestive Carcinoid Tumor", "Recurrent Digestive Carcinoid Tumor", "Relapsed Gastrointestinal Carcinoid Tumor", "Recurrent Gastrointestinal Carcinoid Tumor", "recurrent gastrointestinal carcinoid tumor", "gastrointestinal carcinoid tumor, recurrent", "Recurrent Gastrointestinal Neuroendocrine Tumor G1", "Recurrent Digestive System Neuroendocrine Tumor G1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Digestive System Neuroendocrine Tumor G1", "shortest_name_length": 27}
{"curie": "MONDO:0008241", "names": ["PGP1", "phosphoglycoprotein 1", "PHOSPHOGLYCOPROTEIN 1", "phosphoglycoprotein type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phosphoglycoprotein 1", "shortest_name_length": 4}
{"curie": "MONDO:0013310", "names": ["PORD", "POR Deficiency", "POR deficiency", "Antley-Bixler Syndrome Type 1", "Antley Bixler Syndrome Type 1", "cytochrome P450 oxidoreductase deficiency", "Cytochrome P450 Oxidoreductase Deficiency", "Antley Bixler Syndrome, Autosomal Recessive", "Antley-Bixler Syndrome, Autosomal Recessive", "disordered steroidogenesis due to POR deficiency", "DISORDERED STEROIDOGENESIS DUE TO POR DEFICIENCY", "Antley Bixler Syndrome with Disordered Steroidogenesis", "Antley-Bixler Syndrome with Disordered Steroidogenesis", "congenital adrenal hyperplasia due to cytochrome POR deficiency", "Congenital adrenal hyperplasia due to cytochrome POR deficiency", "Combined Partial Deficiency of 17-Hydroxylase and 21-Hydroxylase", "Combined Partial Deficiency of 17 Hydroxylase and 21 Hydroxylase", "disordered steroidogenesis due to cytochrome P450 oxidoreductase", "Antley-Bixler Syndrome-Like Phenotype With Disordered Steroidogenesis", "Antley Bixler Syndrome Like Phenotype With Disordered Steroidogenesis", "DISORDERED STEROIDOGENESIS DUE TO CYTOCHROME P450 OXIDOREDUCTASE DEFICIENCY", "Disordered Steroidogenesis Due To Cytochrome P450 Oxidoreductase Deficiency", "Disordered Steroidogenesis due to Cytochrome P450 Oxidoreductase Deficiency", "disordered steroidogenesis due to cytochrome P450 oxidoreductase deficiency", "Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency", "Congenital Adrenal Hyperplasia due to Cytochrome P450 Oxidoreductase Deficiency", "congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency", "Adrenal Hyperplasia, Congenital, Due To Cytochrome P450 Oxidoreductase Deficiency", "adrenal hyperplasia, congenital, due to cytochrome P450 oxidoreductase deficiency", "ADRENAL HYPERPLASIA, CONGENITAL, DUE TO CYTOCHROME P450 OXIDOREDUCTASE DEFICIENCY", "Congenital Adrenal Hyperplasia Due To Apparent Combined P450c17 and P450c21 Deficiency", "Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0018671", "names": ["IgG4-related kidney disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IgG4-related kidney disease", "shortest_name_length": 27}
{"curie": "UMLS:C1532715", "names": ["Kappa light chain myeloma", "Kappa Light Chain Myeloma", "Kappa Light Chain Multiple Myeloma", "Kappa light chain myeloma (disorder)", "Kappa light chain myeloma (diagnosis)", "malignant neoplasm multiple myeloma kappa light chain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kappa light chain myeloma", "shortest_name_length": 25}
{"curie": "MONDO:0018825", "names": ["PYCR2-related microcephaly-progressive leukoencephalopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PYCR2-related microcephaly-progressive leukoencephalopathy", "shortest_name_length": 58}
{"curie": "UMLS:C5555082", "names": ["Secondary Peripheral Chondrosarcoma, Grade 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary Peripheral Chondrosarcoma, Grade 3", "shortest_name_length": 44}
{"curie": "UMLS:C0160345", "names": ["injury of GI tract", "Digestive System Injury", "Gastrointestinal injury", "Gastrointestinal Injury", "Gastrointestinal injury NOS", "gastrointestinal tract; injury", "injury; gastrointestinal tract", "Injury of gastrointestinal tract", "Injury to gastrointestinal tract", "injury of gastrointestinal tract", "GIT - Gastrointestinal tract injury", "Injury of gastrointestinal tract, NOS", "Injury of gastrointestinal tract (disorder)", "injury of gastrointestinal tract (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of gastrointestinal tract", "shortest_name_length": 18}
{"curie": "MONDO:0012942", "names": ["LNCR3", "LUNG CANCER SUSCEPTIBILITY 3", "lung cancer susceptibility 3", "adenocarcinoma of lung, susceptibility to", "ADENOCARCINOMA OF LUNG, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung cancer susceptibility 3", "shortest_name_length": 5}
{"curie": "UMLS:C1335041", "names": ["Non-Neoplastic Salivary Gland Disease", "Non-Neoplastic Salivary Gland Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Salivary Gland Disorder", "shortest_name_length": 37}
{"curie": "MONDO:0018127", "names": ["Del(16)(q24.1)", "monosomy 16q24.1", "16q24.1 microdeletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "16q24.1 microdeletion syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0015639", "names": ["benign partial epilepsy with secondarily generalized seizures in infancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign partial epilepsy with secondarily generalized seizures in infancy", "shortest_name_length": 72}
{"curie": "MONDO:0005367", "names": ["Heroin Addiction", "Heroin addiction", "heroin addiction", "addiction heroin", "heroin dependence", "Heroin dependence", "Heroin Dependence", "Addiction, Heroin", "addictions heroin", "heroin; dependence", "Dependence, Heroin", "dependence; heroin", "addiction drug heroin", "Addiction;drug(s);heroin", "opioid dependence heroin", "Dependence on diamorphine", "Heroin dependence (diagnosis)", "Dependence on diamorphine (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heroin dependence", "shortest_name_length": 16}
{"curie": "UMLS:C4085564", "names": ["Prosoposchisis", "PROSOPOSCHISIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prosoposchisis", "shortest_name_length": 14}
{"curie": "MONDO:0007548", "names": ["TBDN", "MONDON", "DEB-BDN", "Self-improving DEB", "transient bullous of the newborn", "DEB, bullous dermolysis of the newborn", "transient bullous dermolysis of newborn", "Transient bullous dermolysis of newborn", "dystrophic epidermolysis bullosa, neonatal", "DYSTROPHIC EPIDERMOLYSIS BULLOSA, NEONATAL", "Transient bullous dermolysis of the newborn", "transient bullous dermolysis of the newborn", "TRANSIENT BULLOUS DERMOLYSIS OF THE NEWBORN", "Self-improving dystrophic epidermolysis bullosa", "epidermolysis bullosa dystrophica, neonatal form", "EPIDERMOLYSIS BULLOSA DYSTROPHICA, NEONATAL FORM", "Transient bullous dermolysis of newborn (disorder)", "Dystrophic Epidermolysis Bullosa, Dominant Neonatal", "transient bullous dermolysis of newborn (diagnosis)", "Epidermolysis bullosa dystrophica, dominant neonatal form", "epidermolysis bullosa dystrophica, dominant neonatal form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transient bullous dermolysis of the newborn", "shortest_name_length": 4}
{"curie": "MONDO:0007925", "names": ["MAR", "5q syndrome", "5q-syndrome", "monosomy 5q", "5q- SYNDROME", "5Q- syndrome", "5q- syndrome", "5q- Syndrome", "del(5q) syndrome", "5q minus syndrome", "5Q minus syndrome", "partial monosomy 5q", "5q deletion syndrome", "5q minus syndrome NOS", "chromosome 5q monosomy", "Chromosome 5q Deletion Syndrome", "chromosome 5q deletion syndrome", "CHROMOSOME 5q DELETION SYNDROME", "Partial monosomy of chromosome 5q", "Partial deletion of chromosome 5q", "MEGAKARYOCYTES, UNILOBULAR NUCLEATED", "megakaryocytes, unilobular nucleated", "Myelodysplastic Syndrome with 5q Deletion", "Myelodysplastic syndrome with 5Q deletion", "myelodysplastic syndrome with 5q deletion", "Myelodysplastic syndrome with 5q deletion", "Myelodysplastic syndrome with 5q- syndrome", "Myelodysplastic Syndrome with Isolated del(5q)", "Myelodysplastic syndrome with isolated del(5q)", "myelodysplastic syndrome with isolated del(5q)", "Refractory macrocytic anemia due to 5q deletion", "refractory macrocytic anemia due to 5q deletion", "Myelodysplastic syndrome with isolated del (5q)", "Partial monosomy of the long arm of chromosome 5", "Partial deletion of the long arm of chromosome 5", "macrocytic Anemia, refractory, due to 5Q deletion", "MACROCYTIC ANEMIA, REFRACTORY, DUE TO 5q DELETION", "Macrocytic Anemia, Refractory, Due To 5q Deletion", "myelodysplastic syndrome with 5q deletion syndrome", "Myelodysplastic syndrome with isolated deletion 5q", "Myelodysplastic syndrome with 5q deletion (5q-) syndrome", "myelodysplastic syndrome associated with isolated del(5q)", "Myelodysplastic syndrome with isolated del(5q) (disorder)", "macrocytic anemia, refractory, due to 5q deletion, somatic", "5q- syndrome, refractory macrocytic anemia due to 5q deletion", "myelodysplastic syndrome with 5q deletion syndrome (diagnosis)", "Myelodysplastic syndrome with isolated del(5q) chromosomal abnormality", "Myelodysplastic syndrome with isolated deletion 5q (morphologic abnormality)", "Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality", "myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality", "myelodysplastic syndrome associated with isolated del (5q) chromosome Abnormality", "Myelodysplastic Syndrome Associated with Isolated del (5q) Chromosome Abnormality"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myelodysplastic syndrome associated with isolated del(5q)", "shortest_name_length": 3}
{"curie": "MONDO:0000359", "names": ["SCD", "SCDO", "SCDO1", "VERTEBRAL ANOMALIES", "Jarcho-Levin syndrome", "JARCHO-LEVIN SYNDROME", "Costovertebral dysplasia", "costovertebral dysplasia", "spondylocostal dysplasia", "COSTOVERTEBRAL DYSPLASIA", "Spondylocostal dysostosis", "Spondylocostal Dysostosis", "spondylocostal dysostosis", "Spondylothoracic Dysplasia", "spondylothoracic dysplasia", "SPONDYLOTHORACIC DYSPLASIA", "Spondylothoracic dysplasia", "spondylothoracic dysostosis", "Spondylothoracic Dysostosis", "SPONDYLOTHORACIC DYSOSTOSIS", "Jarcho-Levin syndrome (disorder)", "SCDO1 Spondylocostal dysostosis 1", "Autosomal recessive spondylocostal dysostosis", "Spondylocostal Dysostosis 1, Autosomal Recessive", "SPONDYLOCOSTAL DYSOSTOSIS 1, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondylocostal dysostosis", "shortest_name_length": 3}
{"curie": "MONDO:0026767", "names": ["IMD74", "TLR7 deficiency", "TLR7 DEFICIENCY", "X-Linked immunodeficiency 74", "X-linked immunodeficiency 74,COVID-19-related", "IMMUNODEFICIENCY 74, COVID19-RELATED, X-LINKED", "immunodeficiency 74, COVID-19-related, X-linked", "RESPIRATORY INSUFFICIENCY DUE TO SARS-CoV-2 VIRAL INFECTION", "respiratory insufficiency due to SARS-CoV-2 viral infection", "immunodeficiency 74, COVID19-related, X-linked, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 74, COVID-19-related, X-linked", "shortest_name_length": 5}
{"curie": "MONDO:0002786", "names": ["Diencephalic Tumor", "diencephalon cancer", "diencephalic cancer", "Tumor of Diencephalon", "tumor of Diencephalon", "Diencephalic Neoplasm", "tumor of diencephalon", "diencephalic neoplasm", "cancer of diencephalon", "Diencephalic Neoplasms", "Neoplasm of Diencephalon", "Tumor of the Diencephalon", "Neoplasm of the Diencephalon", "Malignant Diencephalic Tumor", "malignant diencephalic tumor", "malignant Diencephalic tumor", "malignant diencephalic neoplasm", "malignant diencephalon neoplasm", "Malignant Diencephalic Neoplasm", "malignant diencephalic neoplasms", "Malignant Diencephalic Neoplasms", "malignant neoplasm of diencephalon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diencephalic cancer", "shortest_name_length": 18}
{"curie": "MONDO:0019397", "names": ["unknown leukodystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "unknown leukodystrophy", "shortest_name_length": 22}
{"curie": "UMLS:C1333022", "names": ["Chondrosarcoma NCI Grade 2", "Chondrosarcoma NCI Grade II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chondrosarcoma NCI Grade 2", "shortest_name_length": 26}
{"curie": "MONDO:0006300", "names": ["MMB", "medullomyoblastoma", "Medullomyoblastoma", "Medullomyoblastomas", "Medullomyoblastoma (morphologic abnormality)", "Medullomyoblastoma with Myogenic Differentiation", "medullomyoblastoma with myogenic differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "medullomyoblastoma with myogenic differentiation", "shortest_name_length": 3}
{"curie": "MONDO:0042727", "names": ["presacral teratoma", "Presacral Teratoma", "Presacral teratoma", "Pre-Sacral Teratoma", "pre-sacral teratoma", "teratoma sacrococcygeal", "Sacrococcygeal Teratoma", "sacrococcygeal teratoma", "Sacrococcygeal teratoma", "Sacrococcygeal teratoma (disorder)", "Sacrococcygeal teratoma (diagnosis)", "neoplasm of uncertain behavior of sacrococcygeal region teratoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sacrococcygeal teratoma", "shortest_name_length": 18}
{"curie": "MONDO:0016095", "names": ["vagina rhabdomyosarcoma", "vaginal rhabdomyosarcoma", "Vaginal Rhabdomyosarcoma", "Vulvovaginal rhabdomyosarcoma", "vulvovaginal rhabdomyosarcoma", "vagina rhabdomyosarcoma (disease)", "rhabdomyosarcoma (disease) of vagina", "Rhabdomyosarcoma of vulva and vagina", "Rhabdomyosarcoma of vulva and vagina (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vaginal rhabdomyosarcoma", "shortest_name_length": 23}
{"curie": "UMLS:C3899980", "names": ["BCLC Stage B Hepatocellular Cancer", "BCLC Stage B Adult Hepatocellular Carcinoma", "Barcelona Clinic Liver Cancer Stage B Adult Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "BCLC Stage B Adult Hepatocellular Carcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0056806", "names": ["Non-squamous", "non- squamous NSCLC", "Non-Small Cell Squamous Lung Cancer", "non-small cell squamous lung cancer", "Squamous non-small cell lung cancer", "Lung Non-Small Cell Squamous Carcinoma", "squamous non-small cell lung carcinoma", "Non-Small Cell Squamous Lung Carcinoma", "non-small cell squamous lung carcinoma", "Squamous Non-Small Cell Lung Carcinoma", "Non-squamous non-small cell lung cancer", "Non-Squamous Non-Small Cell Lung Cancer", "Non-Squamous Non-Small Cell Lung Carcinoma", "Lung Non-Squamous Non-Small Cell Carcinoma", "lung non-squamous non-small cell carcinoma", "Squamous NSCLC (non-small cell lung cancer)", "Squamous non-small cell lung cancer (disorder)", "Squamous non-small cell lung cancer (diagnosis)", "lung malignant carcinoma non-small cell squamous"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-small cell squamous lung carcinoma", "shortest_name_length": 12}
{"curie": "UMLS:C0474381", "names": ["Chromatopsia", "CHROMATOPSIA", "chromatopsia", "Chromatopsia (finding)", "Perception of things changing color", "Perception of things changing colour"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chromatopsia", "shortest_name_length": 12}
{"curie": "UMLS:C5237739", "names": ["Resectable Glioblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Glioblastoma", "shortest_name_length": 23}
{"curie": "MONDO:0008543", "names": ["Tetralogy of fallot and glaucoma", "tetralogy of fallot and glaucoma", "TETRALOGY OF FALLOT AND GLAUCOMA", "Familial tetralogy of fallot and glaucoma", "familial tetralogy of fallot and glaucoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tetralogy of fallot and glaucoma", "shortest_name_length": 32}
{"curie": "UMLS:C0856166", "names": ["Suture rupture", "suture; rupture", "Ruptured suture", "rupture; suture"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Suture rupture", "shortest_name_length": 14}
{"curie": "EFO:1000965", "names": ["Henoch-Schoenlein purpura"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Henoch-Schoenlein purpura", "shortest_name_length": 25}
{"curie": "MONDO:0000690", "names": ["Dysmorphophobia", "dysmorphophobia", "body dysmorphia", "BODY IMAGE DISORDER", "Body image disorder", "DISTORTION PERSONAL", "body image disorder", "dysmorphic syndrome", "DISORDER BODY IMAGE", "Disorder body image", "Body Image Disorder", "body disorders image", "Body Image Disorders", "Distortion corporeal", "DISTORTION CORPOREAL", "Image Disorders, Body", "Disorders, Body Image", "Body Image Disfunction", "Image Disfunction, Body", "Body Image Disfunctions", "Disfunction, Body Image", "body disorder dysmorphic", "Disfunctions, Body Image", "body dysmorphic disorder", "Body Dysmorphic Disorder", "Image Disfunctions, Body", "Body dysmorphic disorder", "Disorder, Body Dysmorphic", "body dysmorphic; disorder", "Dysmorphic Disorder, Body", "disorder; body dysmorphic", "Body Dysmorphic Disorders", "Dysmorphic Disorders, Body", "Disorders, Body Dysmorphic", "Nondelusional dysmorphophobia", "Dysmorphophobia (nondelusional)", "Body dysmorphic disorder (disorder)", "body dysmorphic disorder (diagnosis)", "preoccupation with imagined physical defect", "preoccupation with imagined physical defect (symptom)", "preoccupation w/ imagined physical defect (dysmorphophobia)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "body dysmorphic disorder", "shortest_name_length": 15}
{"curie": "UMLS:C4683236", "names": ["Retinoblastoma by AJCC v8 Pathologic Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retinoblastoma by AJCC v8 Pathologic Stage", "shortest_name_length": 42}
{"curie": "MONDO:0019743", "names": ["nephropathy secondary to a storage or other metabolic disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephropathy secondary to a storage or other metabolic disease", "shortest_name_length": 61}
{"curie": "UMLS:C4725603", "names": ["Refractory Chronic Myelomonocytic Leukemia", "Refractory Chronic Myelomonocytic Leukemia (CMML)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Chronic Myelomonocytic Leukemia", "shortest_name_length": 42}
{"curie": "MONDO:0045043", "names": ["disorder of broad ligament", "Disorder of broad ligament", "broad ligament of uterus disease", "disorder of uterine broad ligament", "disease of broad ligament of uterus", "disorder of broad ligament of uterus", "Disorder of broad ligament (disorder)", "broad ligament of uterus disease or disorder", "disease or disorder of broad ligament of uterus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of uterine broad ligament", "shortest_name_length": 26}
{"curie": "MONDO:0042499", "names": ["BFIC1", "BFIS1", "benign familial infantile seizures 1", "benign infantile familial convulsions", "Benign Familial Infantile Seizures, 1", "SEIZURES, BENIGN FAMILIAL INFANTILE, 1", "seizures, benign familial infantile, 1", "Seizures, Benign Familial Infantile, 1", "benign infantile familial convulsions 1", "convulsions, benign familial infantile, 1", "CONVULSIONS, BENIGN FAMILIAL INFANTILE, 1", "Convulsions, Benign Familial Infantile, 1", "benign familial neonatal-infantile seizures 1", "benign familial infantile convulsions syndrome", "benign familial infantile convulsions syndrome 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign familial neonatal-infantile seizures 1", "shortest_name_length": 5}
{"curie": "UMLS:C3640074", "names": ["Spinal Injury Related to Birth", "Spinal Cord Injury Related to Birth", "Spinal Injury Related to Birth Trauma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spinal Injury Related to Birth", "shortest_name_length": 30}
{"curie": "UMLS:C5238957", "names": ["Resectable Glioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Glioma", "shortest_name_length": 17}
{"curie": "MONDO:0023003", "names": ["double fingernail of fifth finger"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "double fingernail of fifth finger", "shortest_name_length": 33}
{"curie": "UMLS:C4682435", "names": ["Stage IIB Vaginal Cancer", "Stage IIB Vaginal Cancer AJCC v8", "Stage IIB Vaginal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Vaginal Cancer AJCC v8", "shortest_name_length": 24}
{"curie": "UMLS:C3146250", "names": ["Stage III Colorectal Cancer", "Stage III Colorectal Cancer AJCC v7", "Stage III Colorectal (Colon or Rectal) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Colorectal Cancer AJCC v7", "shortest_name_length": 27}
{"curie": "UMLS:C0863198", "names": ["Stage I Bladder Cancer with Cancer in situ", "Stage I Bladder Cancer with Carcinoma In Situ", "Bladder carcinoma stage I, with cancer in situ", "Carcinoma bladder stage I, with cancer in situ", "Stage I Bladder Carcinoma with Carcinoma in situ", "Carcinoma urinary bladder stage I, with cancer in situ", "Urinary bladder carcinoma stage I, with cancer in situ"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder carcinoma stage I, with cancer in situ", "shortest_name_length": 42}
{"curie": "MONDO:0004407", "names": ["stroma-dominant and stroma-poor composite ganglioneuroblastoma", "Composite Ganglioneuroblastoma, Stroma-Dominant and Stroma-Poor", "composite ganglioneuroblastoma, Stroma-dominant and Stroma-poor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stroma-dominant and stroma-poor composite ganglioneuroblastoma", "shortest_name_length": 62}
{"curie": "MONDO:0019880", "names": ["trisomy 5qter", "Trisomy 5qter", "distal trisomy 5q", "Distal trisomy 5q", "Distal duplication 5q", "distal duplication 5q", "distal trisomy type 5q", "Telomeric duplication 5q", "telomeric duplication 5q", "Distal trisomy 5q syndrome", "Distal trisomy 5q (diagnosis)", "Distal trisomy 5q syndrome (disorder)", "anomaly of chromosome pair 5 distal trisomy 5q"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal trisomy 5q", "shortest_name_length": 13}
{"curie": "MONDO:0015440", "names": ["R6", "Ring 6", "r(6) syndrome", "ROSE Cluster 6", "rose cluster 6", "chromosome 6 ring", "ring chromosome 6", "Ring chromosome 6", "Ring chromosome type 6", "chromosome 6 ring syndrome", "ring chromosome 6 syndrome", "Ring chromosome 6 syndrome", "Chromosome 6 ring syndrome", "Ring chromosome 6 syndrome (disorder)", "Ring chromosome 6 syndrome (diagnosis)", "anomaly of chromosome pair ring chromosome 6 syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ring chromosome 6", "shortest_name_length": 2}
{"curie": "MONDO:0009367", "names": ["HMCS", "MKKS", "Kaufman-McKusick syndrome", "MCKUSICK-KAUFMAN SYNDROME", "HYDROMETROCOLPOS SYNDROME", "Kaufman-Mckusick syndrome", "Kaufman McKusick syndrome", "hydrometrocolpos syndrome", "Hydrometrocolpos syndrome", "MCKUSICK-Kaufman syndrome", "Kaufman-Mckusick Syndrome", "KAUFMAN-MCKUSICK SYNDROME", "McKusick-Kaufman syndrome", "Mckusick-Kaufman Syndrome", "McKusick Kaufman syndrome", "hydrometrocolpos-postaxial polydactyly syndrome", "Hydrometrocolpos-postaxial polydactyly syndrome", "Hydrometrocolpos, postaxial polydactyly, and congenital heart malformation", "hydrometrocolpos, postaxial polydactyly, and congenital heart malformation", "HYDROMETROCOLPOS, POSTAXIAL POLYDACTYLY, AND CONGENITAL HEART MALFORMATION", "Hydrometrocolpos, postaxial polydactyly, and congenital heart malformation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "McKusick-Kaufman syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C1709592", "names": ["Polymorphus Hemangioendothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Polymorphus Hemangioendothelioma", "shortest_name_length": 32}
{"curie": "UMLS:C4553698", "names": ["Stage IIIC2 Uterine Corpus Cancer AJCC v8", "Stage IIIC2 Uterine (including Endometrial) Cancer", "Stage IIIC2 Uterine Corpus Carcinoma or Carcinosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC2 Uterine Corpus Cancer AJCC v8", "shortest_name_length": 41}
{"curie": "MONDO:0800142", "names": ["chronic mucocutaneous candidiasis and connective tissue disease due to JNK1 haploinsufficiency", "JNK1 haploinsufficiency (causing combination of chronic mucocutaneous candidiasis and connective tissue disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic mucocutaneous candidiasis and connective tissue disease due to JNK1 haploinsufficiency", "shortest_name_length": 94}
{"curie": "MONDO:0025086", "names": ["canine hip dysplasia", "Canine hip dysplasia", "Canine Hip Dysplasia", "hip dysplasia, canine", "Dysplasia, Canine Hip", "Hip Dysplasia, Canine", "dysplasia, canine hip"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hip dysplasia, canine", "shortest_name_length": 20}
{"curie": "UMLS:C4289734", "names": ["CMTC", "Thyroid Gland Cribriform Morular Carcinoma", "Cribriform Morular Thyroid Gland Carcinoma", "Cribriform-Morular Variant Thyroid Gland Papillary Cancer", "Cribriform-Morular Variant Thyroid Gland Papillary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Cribriform Morular Carcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0007638", "names": ["FUCT", "FUCOSIDASE REGULATOR", "fucosidase regulator", "Alpha-L-fucosidase regulator", "ALPHA-L-FUCOSIDASE REGULATOR"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fucosidase regulator", "shortest_name_length": 4}
{"curie": "MONDO:0009073", "names": ["RTSC", "RTSC1", "3C syndrome", "Ritscher-Schinzel syndrome", "Ritscher-Schinzel syndrome 1", "RITSCHER-SCHINZEL SYNDROME 1", "Craniocerebellocardiac dysplasia", "Ritscher-Schinzel syndrome type 1", "WASHC5 Ritscher-Schinzel syndrome", "Ritscher-Schinzel syndrome caused by mutation in WASHC5", "Dandy-Walker-like malformation with atrioventricular septal defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ritscher-Schinzel syndrome 1", "shortest_name_length": 4}
{"curie": "MONDO:0023628", "names": ["Anorectal spasm", "anorectal spasm", "proctalgia fugax", "Proctalgia fugax", "LEVATOR SYNDROME", "Proctalgia Fugax", "levator syndrome", "Levator syndrome", "fugax proctalgia", "fugax; proctalgia", "proctalgia; fugax", "levator ani syndrome", "Levator ani syndrome", "Paroxysmal proctalgia", "spasmodic; proctalgia", "Painful spasm of anus", "proctalgia; spasmodic", "paroxysmal proctalgia", "painful spasm of anus", "Psychogenic anal spasm", "psychogenic anal spasm", "levator ani spasm syndrome", "Levator ani spasm syndrome", "proctalgia fugax (diagnosis)", "levator ani syndrome (diagnosis)", "Painful spasm of anus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "levator syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0008129", "names": ["Ophthalmoplegia, Familial Total, with Iris Transillumination", "OPHTHALMOPLEGIA, FAMILIAL TOTAL, WITH IRIS TRANSILLUMINATION", "ophthalmoplegia, familial total, with iris transillumination"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ophthalmoplegia, familial total, with iris transillumination", "shortest_name_length": 60}
{"curie": "MONDO:0005020", "names": ["Enteropathy", "enteropathy", "Disease;bowel", "disease bowel", "BOWEL DISEASE", "bowel disease", "bowels disease", "bowel; disease", "bowel disorder", "bowel diseases", "bowels diseases", "disorders bowel", "bowel disorders", "Bowel Disorders", "bowels disorders", "Enteropathy, NOS", "bowel dysfunction", "disease intestine", "intestine disease", "Intestinal disease", "Intestinal Disease", "disease intestines", "diseases intestine", "disease intestinal", "disorder intestine", "intestinal disease", "intestine disorder", "intestine; disease", "intestinal disorder", "disorders intestine", "Intestinal Disorder", "Intestinal Diseases", "intestinal diseases", "diseases intestines", "Disease, Intestinal", "disease, intestinal", "disorder intestinal", "disorders intestinal", "disorders intestines", "intestinal disorders", "Intestines--Diseases", "diseases, intestinal", "disease of intestine", "Diseases, Intestinal", "Disorder of intestine", "disorder of intestine", "diseases intestinal tract", "intestinal tract diseases", "Disease of intestine, NOS", "disease (or disorder); bowel", "Abnormality of the intestine", "intestine disease or disorder", "Abnormal intestine morphology", "intestinal disorder (diagnosis)", "disease or disorder of intestine", "Disorder of intestine (disorder)", "diseases of the intestinal tract", "DISEASES OF THE INTESTINAL TRACT", "disease (or disorder); intestine", "Disease of intestine, unspecified", "Unspecified disorder of intestine", "DISEASES OF THE SMALL AND LARGE INTESTINES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intestinal disorder", "shortest_name_length": 11}
{"curie": "MONDO:0005498", "names": ["botulism", "Botulism", "BOTULISM", "botulisms", "Lamziekte", "Loin disease", "Botulism NOS", "Lame sickness", "foodborne botulism", "botulism poisoning", "Foodborne botulism", "Botulism poisoning", "botulism (diagnosis)", "Clostridium; botulinum", "wound botulism (subtype)", "infant botulism (subtype)", "Toxico-Infectious Botulism", "Toxico Infectious Botulism", "Botulism, Toxico-Infectious", "Botulism, Toxico Infectious", "foodborne botulism (subtype)", "Clostridium botulinum poisoning", "Clostridium botulinum Infection", "Infection, Clostridium botulinum", "Clostridium botulinum Infections", "poisoning; Clostridium botulinum", "Clostridium; botulinum, poisoning", "infection due to Clostridium botulinum", "Infection due to Clostridium botulinum", "Infection due to clostridium botulinum", "Infection caused by Clostridium botulinum", "Food poisoning due to Clostridium botulinum", "food poisoning due to Clostridium botulinum", "intoxication with Clostridium botulinum toxin", "Intoxication with Clostridium botulinum toxin", "Infection caused by Clostridium botulinum (disorder)", "Botulism due to infection with Clostridium botulinum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "botulism", "shortest_name_length": 8}
{"curie": "UMLS:C5239087", "names": ["Familial MDS", "Familial Myelodysplastic Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Familial Myelodysplastic Syndrome", "shortest_name_length": 12}
{"curie": "UMLS:C4688666", "names": ["Stage IIIA Posterior Uveal Melanoma AJCC v8", "Stage IIIA Choroidal and Ciliary Body Melanoma", "Stage IIIA Choroidal and Ciliary Body Melanoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Choroidal and Ciliary Body Melanoma AJCC v8", "shortest_name_length": 43}
{"curie": "UMLS:C1333941", "names": ["Head and Neck Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Head and Neck Disorder", "shortest_name_length": 22}
{"curie": "UMLS:C0560619", "names": ["Periocular injury", "Injury of eye region", "Injury of eye region (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of eye region", "shortest_name_length": 17}
{"curie": "UMLS:C0796623", "names": ["stage III soft tissue sarcoma", "Stage III Soft Tissue Sarcoma", "Stage III Sarcoma of Soft Tissue", "Stage III Sarcoma of the Soft Tissue", "Stage III Soft Tissue Sarcoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Soft Tissue Sarcoma AJCC v7", "shortest_name_length": 29}
{"curie": "UMLS:C0431334", "names": ["Lumbar Myelocele", "Lumbar myelocele", "Lumbar myelocele (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lumbar myelocele", "shortest_name_length": 16}
{"curie": "MONDO:0006897", "names": ["ICC", "Dental Cyst", "dental cyst", "apical cyst", "Dental cyst", "Apical cyst", "Dental cysts", "Lateral Cyst", "cysts dental", "cyst; apical", "cyst lateral", "Cyst, Lateral", "Lateral Cysts", "Cysts, Lateral", "Radicular cyst", "radicular cyst", "Radicular Cyst", "radicular cysts", "Paradental cyst", "periapical cyst", "radicular; cyst", "Cyst, Radicular", "Radicular Cysts", "cyst; radicular", "Periapical cyst", "Periapical Cyst", "periapical cysts", "Cyst, Periapical", "Dental granuloma", "Periapical Cysts", "periodontal cyst", "cyst; periapical", "Dental Granuloma", "Apical granuloma", "periapical; cyst", "dental granuloma", "Dental Root Cyst", "Periodontal Cyst", "Periodontal cyst", "cyst periodontal", "Cysts, Radicular", "apical granuloma", "Dental Granulomas", "periodontal cysts", "granuloma; dental", "dental; granuloma", "cyst; periodontal", "Periapical lesion", "Granuloma, Dental", "Cyst, Periodontal", "dental root; cyst", "Cyst, Dental Root", "periodontal; cyst", "granuloma; apical", "Periodontal Cysts", "Cysts, Periapical", "Root Cyst, Dental", "cyst; dental root", "Dental Root Cysts", "Periradicular cyst", "Granulomas, Dental", "Dentoalveolar Cyst", "Cysts, Dental Root", "Root Cysts, Dental", "periradicular cyst", "Cysts, Periodontal", "Radiculodental cyst", "Cyst, Dentoalveolar", "Dentoalveolar Cysts", "Periapical bone loss", "Cysts, Dentoalveolar", "Periapical Granuloma", "periapical granuloma", "Periapical granuloma", "Apical radicular cyst", "apical radicular cyst", "Radicular cyst dental", "granuloma; periapical", "Periapical Granulomas", "Granuloma, Periapical", "periapical; granuloma", "Granulomas, Periapical", "Apical periodontal cyst", "Apical Periodontal Cyst", "Periapical radiolucency", "residual radicular cyst", "Residual radicular cyst", "Inflammatory Dental Cyst", "Apical Periodontal Cysts", "Periodontal Cyst, Apical", "Cyst, Apical Periodontal", "Radicular cyst (disorder)", "Periapical radiolucencies", "periapical radicular cyst", "Cysts, Apical Periodontal", "Periodontal Cysts, Apical", "Apical (periodontal) cyst", "radicular cyst (diagnosis)", "Cyst of periodontal tissue", "Bone loss around tooth root", "Apical granuloma (disorder)", "Periodontal odontogenic cyst", "Inflammatory Collateral Cyst", "Inflammatory collateral cyst", "Mandibular infected buccal cyst", "apical radicular cyst (diagnosis)", "residual radicular cyst (diagnosis)", "Dark spot around tooth root on x-ray", "periapical radicular cyst (diagnosis)", "Cyst of periodontal tissue (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "periapical granuloma", "shortest_name_length": 3}
{"curie": "MONDO:0006580", "names": ["miliaria", "MILIARIA", "Miliaria", "Heat Rash", "heat rash", "sweat rash", "prickly heat", "Prickly Heat", "Miliaria, NOS", "eccrine miliaria", "Miliaria (disorder)", "miliaria (diagnosis)", "Miliaria, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "miliaria", "shortest_name_length": 8}
{"curie": "UMLS:C0700509", "names": ["Chronic peptic ulcer", "chronic peptic ulcer", "ulcer; peptic, chronic", "Chronic peptic ulcer (disorder)", "chronic peptic ulcer (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic peptic ulcer", "shortest_name_length": 20}
{"curie": "MONDO:0017750", "names": ["defect in COG complex", "defect in conserved oligomeric Golgi complex"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "defect in conserved oligomeric Golgi complex", "shortest_name_length": 21}
{"curie": "UMLS:C2983008", "names": ["Stage I Uterine Corpus Cancer", "Stage I Uterine Corpus Cancer AJCC v7", "Stage I Uterine (including Endometrial) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Uterine Corpus Cancer", "shortest_name_length": 29}
{"curie": "UMLS:C0730349", "names": ["Abnormal uterine bleeding unrelated to menstrual cycle", "Abnormal uterine bleeding unrelated to menstrual cycle (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abnormal uterine bleeding unrelated to menstrual cycle", "shortest_name_length": 54}
{"curie": "UMLS:C0276727", "names": ["lymphocutaneous sporotrichosis", "Lymphocutaneous sporotrichosis", "SPOROTRICHOSIS LYMPHOCUTANEOUS", "sporotrichosis; lymphocutaneous", "lymphocutaneous; sporotrichosis", "Lymphocutaneous sporotrichosis (disorder)", "lymphocutaneous sporotrichosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphocutaneous sporotrichosis", "shortest_name_length": 30}
{"curie": "MONDO:0005132", "names": ["CMV", "cmv infection", "CMV INFECTION", "CMV infection", "CMV Infection", "HCMV infection", "CMV Infections", "cmv infections", "HCMV Infection", "Cytomegalovirus", "cytomegalovirus", "Inclusion Disease", "inclusion disease", "Inclusion Diseases", "Cytomegalovirus (CMV)", "Cytomegaloviral disease", "Cytomegalovirus disease", "cytomegaloviral disease", "cytomegalovirus disease", "Cytomegaloviral Infection", "cytomegalovirus infection", "CYTOMEGALOVIRUS INFECTION", "cytomegaloviral infection", "Cytomegalovirus Infection", "Cytomegalovirus infection", "Cytomegaloviral infection", "cytomegalovirus infections", "Cytomegaloviral infections", "Infection, Cytomegalovirus", "cytomegaloviral infections", "Cytomegalovirus infections", "Cytomegalovirus Infections", "CYTOMEGALUS VIRUS INFECTION", "Infections, Cytomegalovirus", "Salivary Gland Virus Disease", "Salivary gland virus disease", "CYTOMEGALIC INCLUSION DISEASE", "cmv cytomegalovirus infection", "Cytomegalic Inclusion Disease", "cytomegalic inclusion disease", "Cytomegalic inclusion disease", "Disease due to Cytomegalovirus", "Cytomegalovirus infection, NOS", "Disease, Cytomegalic Inclusion", "Cytomegalic Inclusion Diseases", "Inclusion Disease, Cytomegalic", "CMV - Cytomegalovirus infection", "Cytomegalovirus Inclusion Disease", "salivary gland; inclusion disease", "inclusion disease; salivary gland", "Disease, Cytomegalovirus Inclusion", "Cytomegalovirus Inclusion Diseases", "Inclusion Disease, Cytomegalovirus", "Diseases, Cytomegalovirus Inclusion", "Inclusion Diseases, Cytomegalovirus", "cytomegalovirus disease (diagnosis)", "Cytomegalovirus infection (disorder)", "Cytomegaloviral disease, unspecified", "disease (or disorder); inclusion disease, salivary gland", "disease (or disorder); inclusion disease (cytomegaloviral)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cytomegalovirus infection", "shortest_name_length": 3}
{"curie": "MONDO:0016530", "names": ["Laryngocele", "laryngocele", "Laryngoceles", "laryngoceles", "laryngocele congenital", "congenital laryngocele", "Congenital laryngocele", "Congenital laryngocele (disorder)", "congenital laryngocele (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laryngocele", "shortest_name_length": 11}
{"curie": "MONDO:0002892", "names": ["skull base chordoma", "Skull Base Chordoma", "Chordoma of Skull Base", "chordoma of skull base", "chordoma of the skull base", "Chordoma of the Skull Base"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skull base chordoma", "shortest_name_length": 19}
{"curie": "MONDO:0100128", "names": ["coinfection", "Coinfection", "Co-infection", "Coinfections", "Co infection", "Co-infections", "mix infection", "Polyinfection", "mixed infection", "Mixed infection", "Mixed Infection", "Infection mixed", "Mixed infections", "infections mixed", "Infection, Mixed", "Infection, mixed", "Mixed Infections", "Infections, Mixed", "Polyinfection, NOS", "Mixed infection, NOS", "Polymicrobial Infection", "Polymicrobial infection", "polymicrobial infection", "Polymicrobial infections", "Polymicrobial Infections", "Mixed infectious disease", "mixed infectious disease", "Infection, Polymicrobial", "Infections, Polymicrobial", "Mixed infectious disease, NOS", "Mixed infectious disease (disorder)", "mixed infectious disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coinfection", "shortest_name_length": 11}
{"curie": "UMLS:C5557184", "names": ["Stage IVB Cervical Cancer AJCC v9", "Stage IVB Cervical Carcinoma AJCC v9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Cervical Cancer AJCC v9", "shortest_name_length": 33}
{"curie": "UMLS:C5418798", "names": ["Locally Advanced Penile Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Penile Carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0007880", "names": ["web larynx", "larynx web", "web; larynx", "larynx; web", "LARYNGEAL WEB", "web of larynx", "Web of larynx", "laryngeal web", "Laryngeal Web", "Laryngeal web", "SUBGLOTTIC BAR", "Subglottic web", "SUBGLOTTIC WEB", "subglottic web", "laryngeal webs", "Laryngeal webs", "subglottic Bar", "Web of larynx, NOS", "LARYNGEAL WEB, FAMILIAL", "laryngeal web, familial", "Laryngeal Web, Familial", "congenital laryngeal web", "Laryngeal web (disorder)", "Subglottic web (disorder)", "laryngeal web (diagnosis)", "Partial laryngeal atresia", "Gay Feinmesser Cohen syndrome", "gay Feinmesser Cohen syndrome", "GLOTTIC WEB, CONGENITAL ANTERIOR", "Glottic Web, Congenital Anterior", "glottic web, congenital anterior", "larynx; deformity, web (membrane)", "deformity; larynx, web (membrane)", "subglottic web (physical finding)", "Laryngeal web, congenital heart disease and low stature", "laryngeal web, congenital heart disease and low stature", "Subglottic bar, congenital heart disease and low stature", "subglottic bar, congenital heart disease and low stature"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital laryngeal web", "shortest_name_length": 10}
{"curie": "MONDO:0043156", "names": ["Glastre Cochat Bouvier syndrome", "nephrotic syndrome ocular anomalies", "Nephrotic syndrome ocular anomalies", "Familial infantile nephrotic syndrome with ocular abnormalities", "familial infantile nephrotic syndrome with ocular abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrotic syndrome ocular anomalies", "shortest_name_length": 31}
{"curie": "MONDO:0014770", "names": ["JBTS25", "JOUBERT SYNDROME 25", "Joubert syndrome 25", "CEP104 Joubert syndrome", "Joubert syndrome type 25", "Joubert syndrome caused by mutation in CEP104"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome 25", "shortest_name_length": 6}
{"curie": "UMLS:C1334276", "names": ["Invasive Ductal and Invasive Lobular Breast Carcinoma", "Infiltrating Ductal and Infiltrating Lobular Breast Carcinoma", "Invasive Breast Ductal Carcinoma and Invasive Lobular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Invasive Breast Ductal Carcinoma and Invasive Lobular Carcinoma", "shortest_name_length": 53}
{"curie": "UMLS:C1518078", "names": ["Lymphoma by Working Formulation (Antiquated)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoma by Working Formulation (Antiquated)", "shortest_name_length": 44}
{"curie": "UMLS:C0042376", "names": ["VASCULAR HEADACHE", "Headache vascular", "headache vascular", "Vascular Headache", "vascular headache", "Headache;vascular", "Vascular headache", "HEADACHE VASCULAR", "Headache, Vascular", "vascular headaches", "Vascular Cephalgia", "vascular; headache", "headaches vascular", "HEADACHE, VASCULAR", "Vascular Headaches", "headache; vascular", "Vascular Cephalgias", "Cephalgia, Vascular", "Headaches, Vascular", "Cephalgias, Vascular", "Vascular headache (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vascular Headaches", "shortest_name_length": 17}
{"curie": "MONDO:0016215", "names": ["spastic tetraplegia", "Spastic tetraplegia", "Spastic Tetraplegia", "spastic quadriplegia", "Spastic quadriplegia", "spastic quadraplegia", "Spastic quadraplegia", "Spastic Tetraplegias", "spastic; tetraplegia", "tetraplegia; spastic", "quadriplegia spastic", "Tetraplegia, Spastic", "Spastic Quadriplegia", "quadriplegia; spastic", "spastic; quadriplegia", "Tetraplegias, Spastic", "Spastic Quadriplegias", "Quadriplegia, Spastic", "Quadriplegias, Spastic", "Congenital tetraplegia", "Congenital quadriplegia", "congenital; quadriplegia", "Spastic tetraplegia syndrome", "Spastic tetraplegia (disorder)", "Spastic quadriplegia (diagnosis)", "Congenital quadriplegia (disorder)", "spastic tetraplegia cerebral palsy", "spastic quadriplegic cerebral palsy", "Tetraplegic infantile cerebral palsy", "tetraplegic infantile cerebral palsy", "Quadriplegic Infantile Cerebral Palsy", "quadriplegic infantile cerebral palsy", "Quadriplegic infantile cerebral palsy", "Infantile Cerebral Palsy, Quadriplegic", "Infantile cerebral palsy, quadriplegic", "Cerebral Palsy, Quadriplegic, Infantile", "inherited congenital spastic tetraplegia", "inherited congenital spastic quadriplegia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic quadriplegic cerebral palsy", "shortest_name_length": 19}
{"curie": "MONDO:0012077", "names": ["ALS8", "ALS8 (diagnosis)", "AMYOTROPHIC LATERAL SCLEROSIS 8", "Amyotrophic Lateral Sclerosis 8", "amyotrophic lateral sclerosis 8", "amyotrophic lateral sclerosis ALS8", "VAPB amyotrophic lateral sclerosis", "amyotrophic lateral sclerosis type 8", "AMYOTROPHIC LATERAL SCLEROSIS 8 (disorder)", "amyotrophic lateral sclerosis caused by mutation in VAPB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyotrophic lateral sclerosis type 8", "shortest_name_length": 4}
{"curie": "MONDO:0006570", "names": ["Lichen", "LICHEN", "lichen", "Lichen NOS", "lichen skin", "Lichen, NOS", "lichen disease", "Lichen disease", "Lichen condition", "lichen condition", "Lichen (disorder)", "Lichen unspecified", "lichen (diagnosis)", "Lichen, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lichen disease", "shortest_name_length": 6}
{"curie": "UMLS:C1520077", "names": ["Vulvar Congenital Melanocytic Nevus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Congenital Melanocytic Nevus", "shortest_name_length": 35}
{"curie": "UMLS:C0276667", "names": ["systemic coccidioidomycosis", "Generalized coccidioidomycosis", "disseminated coccidioidomycosis", "COCCIDIOIDOMYCOSIS DISSEMINATED", "coccidioidomycosis disseminated", "generalized; coccidioidomycosis", "Disseminated coccidioidomycosis", "coccidioidomycosis; generalized", "disseminated; coccidioidomycosis", "coccidioidomycosis; disseminated", "Extra-pulmonary coccidioidomycosis", "Disseminated coccidioidomycosis (disorder)", "disseminated coccidioidomycosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disseminated coccidioidomycosis", "shortest_name_length": 27}
{"curie": "MONDO:0008023", "names": ["Furukawa Takagi Nakao syndrome", "Furukawa-Takagi-Nakao syndrome", "muscular atrophy ataxia retinitis pigmentosa and diabetes mellitus", "muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus", "Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus", "Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus", "MUSCULAR ATROPHY, ATAXIA, RETINITIS PIGMENTOSA, AND DIABETES MELLITUS", "muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome", "Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome", "shortest_name_length": 30}
{"curie": "UMLS:C4721209", "names": ["HER2 positive metastatic breast cancer", "Metastatic human epidermal growth factor 2 positive carcinoma of breast", "Metastasis from human epidermal growth factor 2 positive carcinoma of breast", "Metastasis from human epidermal growth factor 2 positive carcinoma of breast (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic human epidermal growth factor 2 positive carcinoma of breast", "shortest_name_length": 38}
{"curie": "EFO:1001483", "names": ["non-obstructive coronary artery disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-obstructive coronary artery disease", "shortest_name_length": 39}
{"curie": "MONDO:0015134", "names": ["Kostmann disease", "Kostmann syndrome", "Kostmann neutropenia", "Congenital Neutropenia", "congenital neutropenia", "constitutional neutropenia", "genetic infantile agranulocytosis", "infantile genetic agranulocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "constitutional neutropenia", "shortest_name_length": 16}
{"curie": "OMIM:300910", "names": ["BMND18", "BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 18", "OSTEOPOROSIS AND OSTEOPOROTIC FRACTURES, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 6}
{"curie": "UMLS:C0280361", "names": ["Stage IV Mouth Mucoepidermoid Carcinoma", "Stage IV Oral Cavity Mucoepidermoid Cancer", "Stage IV Mucoepidermoid Carcinoma of Mouth", "Stage IV Oral Cavity Mucoepidermoid Carcinoma", "Stage IV Mucoepidermoid Carcinoma of the Mouth", "oral cavity mucoepidermoid carcinoma, stage IV", "Stage IV Mucoepidermoid Carcinoma of Oral Cavity", "oral cavity mucoepidermoid carcinoma, metastatic", "stage IV mucoepidermoid carcinoma of the oral cavity", "Mucoepidermoid carcinoma of the oral cavity stage IV", "Stage IV Mucoepidermoid Carcinoma of the Oral Cavity", "Stage IV Oral Cavity Mucoepidermoid Carcinoma AJCC v7", "Stage IV Oral Cavity Mucoepidermoid Carcinoma AJCC v6", "mucoepidermoid carcinoma of the oral cavity, stage IV", "metastatic mucoepidermoid carcinoma of the oral cavity", "mucoepidermoid carcinoma of the oral cavity, metastatic", "Stage IV Oral Cavity Mucoepidermoid Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Oral Cavity Mucoepidermoid Carcinoma AJCC v6 and v7", "shortest_name_length": 39}
{"curie": "MONDO:0007614", "names": ["FEOM", "Cfeom", "CFEOM", "CFEOM1", "Feom1 locus", "Tukel syndrome", "General Fibrosis Syndrome", "General fibrosis syndrome", "Congenital ophthalmoplegia", "ophthalmoplegia, congenital", "Congenital fibrosis syndrome", "Congenital fibrosis syndrome (disorder)", "blepharoptosis with absent eye movements", "congenital fibrosis of extraocular muscles", "Congenital fibrosis of extraocular muscles", "fibrosis of extraocular muscles, congenital", "fibrosis of extraocular muscles, congenital, 1", "congenital fibrosis of the extraocular muscles", "Congenital Fibrosis of the Extraocular Muscles", "Congenital fibrosis of the extraocular muscles", "fibrosis of extraocular muscles, congenital, 3B", "Congenital fibrosis of extraocular muscles (CFEOM)", "fibrosis of extraocular muscles, congenital, type 1", "Congenital fibrosis of the extraocular muscles (CFEOM)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital fibrosis of extraocular muscles", "shortest_name_length": 4}
{"curie": "MONDO:0018191", "names": ["tumor of testis and paratestis", "testicular and paratesticular tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tumor of testis and paratestis", "shortest_name_length": 30}
{"curie": "UMLS:C2030691", "names": ["Gallbladder Hepatoid Adenocarcinoma", "hepatoid adenocarcinoma of gallbladder", "hepatoid adenocarcinoma of gallbladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatoid adenocarcinoma of gallbladder", "shortest_name_length": 35}
{"curie": "UMLS:C5421257", "names": ["Metastatic Distal Esophagus Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Distal Esophagus Adenocarcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0024990", "names": ["swine disease", "Swine Disease", "disease, swine", "Disease, Swine", "Swine Diseases", "Diseases, Swine", "Swine--Diseases", "diseases, swine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "swine disease", "shortest_name_length": 13}
{"curie": "MONDO:0022762", "names": ["Deletion 4p", "4p monosomy", "monosomy 4p", "deletion 4p", "Monosomy 4p", "4p deletion", "partial monosomy 4p", "Chromosome 4p deletion", "chromosome 4p deletion", "Chromosome 4 short arm deletion", "chromosome 4 short arm deletion", "partial deletion of chromosome 4p", "partial monosomy of chromosome 4p", "partial deletion of the short arm of chromosome 4", "partial monosomy of the short arm of chromosome 4", "partial deletion of the short arm of chromosome type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 4 short arm deletion", "shortest_name_length": 11}
{"curie": "UMLS:C5419810", "names": ["Liver MANEC", "Liver Mixed Adenoneuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liver Mixed Adenoneuroendocrine Carcinoma", "shortest_name_length": 11}
{"curie": "MONDO:0026777", "names": ["VEXAS", "VEXAS SYNDROME", "VEXAS Syndrome", "VEXAS syndrome", "VEXAS syndrome, somatic", "Vacuoles, E1 enzyme, X-linked, Autoinflammatory, Somatic Syndrome", "vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic syndrome", "vacuoles, E1 enzyme, X-linked, autoinflammatory and somatic syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "VEXAS syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0035475", "names": ["EPHB4-related LRHF/GLD", "EPHB4-related lymphatic-related hydrops fetalis", "EPHB4-related generalized lymphatic dysplasia with atrial septal defect", "EPHB4-related generalized lymphatic dysplasia with non-immune hydrops fetalis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "EPHB4-related lymphatic-related hydrops fetalis", "shortest_name_length": 22}
{"curie": "MONDO:0016411", "names": ["hypothyroidism due to deficient transcription factors involved in pituitary development or function"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypothyroidism due to deficient transcription factors involved in pituitary development or function", "shortest_name_length": 99}
{"curie": "UMLS:C5206406", "names": ["Clonal hematopoiesis", "Clonal Hematopoiesis", "Hematopoiesis, Clonal", "Clonal haematopoiesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clonal Hematopoiesis", "shortest_name_length": 20}
{"curie": "UMLS:C0863093", "names": ["cold symptom", "cold symptoms", "Cold symptoms", "symptoms cold"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cold symptoms", "shortest_name_length": 12}
{"curie": "MONDO:0019714", "names": ["isolated polydactyly, syndactyly and/or hyperphalangy", "nonsyndromic polydactyly, syndactyly and/or hyperphalangy", "non-syndromic polydactyly, syndactyly and/or hyperphalangy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-syndromic polydactyly, syndactyly and/or hyperphalangy", "shortest_name_length": 53}
{"curie": "UMLS:C4553789", "names": ["stage IV ureter cancer", "Stage IV Ureter Cancer", "Stage IV Ureter Cancer AJCC v8", "stage IV ureter cancer AJCC v8", "stage IV ureter urothelial carcinoma AJCC v8", "Stage IV Ureter Urothelial Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Ureter Cancer AJCC v8", "shortest_name_length": 22}
{"curie": "MONDO:0014592", "names": ["MCCRP3", "microcephaly and chorioretinopathy 3", "microcephaly and chorioretinopathy type 3", "TUBGCP4 microcephaly and chorioretinopathy", "MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 3", "microcephaly and chorioretinopathy, autosomal recessive, 3", "microcephaly and chorioretinopathy, autosomal recessive, type 3", "microcephaly and chorioretinopathy caused by mutation in TUBGCP4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly and chorioretinopathy 3", "shortest_name_length": 6}
{"curie": "MONDO:0012717", "names": ["HOMG4", "renal hypomagnesemia 4", "Hypomagnesemia 4, Renal", "hypomagnesemia 4, renal", "HYPOMAGNESEMIA 4, RENAL", "EGF primary hypomagnesemia", "renal hypomagnesemia type 4", "EGF familial primary hypomagnesemia", "Hypomagnesemia, Renal, Normocalciuric", "HYPOMAGNESEMIA, RENAL, NORMOCALCIURIC", "hypomagnesemia, renal, Normocalciuric", "primary hypomagnesemia caused by mutation in EGF", "familial primary hypomagnesemia caused by mutation in EGF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal hypomagnesemia 4", "shortest_name_length": 5}
{"curie": "UMLS:C1623038", "names": ["Cirrhosis", "Cirrhoses"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cirrhosis", "shortest_name_length": 9}
{"curie": "MONDO:0030517", "names": ["TTD8", "TRICHOTHIODYSTROPHY 8, NONPHOTOSENSITIVE", "trichothiodystrophy 8, nonphotosensitive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichothiodystrophy 8, nonphotosensitive", "shortest_name_length": 4}
{"curie": "MONDO:0024482", "names": ["Eccrine Sweat Gland Hamartoma", "eccrine sweat gland hamartoma", "hamartoma of eccrine sweat gland", "Hamartoma of Eccrine Sweat Gland", "Hamartoma of the Eccrine Sweat Gland", "hamartoma of the eccrine sweat gland", "eccrine sweat gland hamartoma (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eccrine sweat gland hamartoma", "shortest_name_length": 29}
{"curie": "MONDO:0020458", "names": ["HAEADA", "ERYTHROCYTE ADA, ELEVATED, HEMOLYTIC ANEMIA DUE TO", "adenosine deaminase, elevated, hemolytic anemia due to", "ADENOSINE DEAMINASE, ELEVATED, HEMOLYTIC ANEMIA DUE TO", "Adenosine Deaminase, Elevated, Hemolytic Anemia Due To", "hemolytic anemia due to erythrocyte adenosine deaminase overproduction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemolytic anemia due to erythrocyte adenosine deaminase overproduction", "shortest_name_length": 6}
{"curie": "MONDO:0007448", "names": ["DDU", "VBU", "Dermagraphy", "dermagraphy", "skin writing", "Autographism", "Dermographia", "dermographia", "DERMOGRAPHIA", "Skin writing", "autographism", "AUTOGRAPHISM", "Dermographism", "DERMOGRAPHISM", "dermatography", "dermographism", "Dermatography", "dermatographia", "DERMATOGRAPHIA", "Dermatographia", "dermatographic", "DERMATOGRAPHISM", "Dermatographism", "dermatographism", "Urticaria factitia", "physical urticaria", "urticaria physical", "Physical urticaria", "urticaria factitia", "Ebbecke's reaction", "physical urticarias", "urticaria; factitia", "factitial urticaria", "Factitial urticaria", "factitia; urticaria", "vibratory urticaria", "factitious urticaria", "vibratory angioedema", "Dermographic prurigo", "Factitious urticaria", "urticaria; artificial", "artificial; urticaria", "Dermographic urticaria", "dermographic urticaria", "familial dermographism", "Familial dermographism", "dermographism, familial", "familial dermatographia", "DERMOGRAPHISM, FAMILIAL", "Dermographism, Familial", "Familial dermatographism", "urticaria dermatographic", "Dermatographic urticaria", "familial dermatographism", "dermatographic urticaria", "symptomatic dermographism", "urticaria; dermatographic", "dermatographic; urticaria", "Symptomatic dermographism", "Dermatographism, familial", "Dermatographism, Familial", "Dermodistortive urticaria", "DERMATOGRAPHISM, FAMILIAL", "dermo-distortive urticaria", "familial dermographic urticaria", "dermatographia (physical finding)", "Dermatographic urticaria (disorder)", "dermatographic urticaria (diagnosis)", "Symptomatic dermographism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial dermatographia", "shortest_name_length": 3}
{"curie": "MONDO:0700002", "names": ["ATP1A3 neurological disorder", "ATP1A3 related neurological disorder", "ATP1A3-associated neurological disorder", "neurological disorder caused by mutation in ATP1A3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ATP1A3-associated neurological disorder", "shortest_name_length": 28}
{"curie": "MONDO:0019002", "names": ["LDD", "Lhermitte-Duclos disease", "Lhermitte Duclos Disease", "Lhermitte-Duclos Disease", "LHERMITTE-DUCLOS DISEASE", "Lhermitte-Duclos disease (disorder)", "Cerebellum Dysplastic Gangliocytoma", "Dysplastic Cerebellar Gangliocytoma", "Dysplastic cerebellar gangliocytoma", "dysplastic cerebellar gangliocytoma", "Lhermitte-Duclos disease (diagnosis)", "Cerebellum Dysplastic Gangliocytomas", "Dysplastic Gangliocytoma of Cerebellum", "dysplastic gangliocytoma of cerebellum", "dysplastic gangliocytoma of the cerebellum", "DYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM", "Dysplastic gangliocytoma of the cerebellum", "Dysplastic Gangliocytoma of the Cerebellum", "Dysplastic gangliocytoma of cerebellum (Lhermitte-Duclos)", "Dysplastic Cerebellar Gangliocytoma (Lhermitte-Duclos Disease)", "Dysplastic gangliocytoma of cerebellum (Lhermitte-Duclos) (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lhermitte-Duclos disease", "shortest_name_length": 3}
{"curie": "MONDO:0000111", "names": ["camptodactyly syndrome, Guadalajara"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "camptodactyly syndrome, Guadalajara", "shortest_name_length": 35}
{"curie": "MONDO:0031200", "names": ["Bryant-Li-Bhoj neurodevelopmental syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bryant-Li-Bhoj neurodevelopmental syndrome", "shortest_name_length": 42}
{"curie": "UMLS:C5555679", "names": ["Unresectable Plexiform Neurofibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Plexiform Neurofibroma", "shortest_name_length": 35}
{"curie": "UMLS:C4744586", "names": ["FTC, Encapsulated Angioinvasive", "Thyroid Gland Follicular Carcinoma, Encapsulated Angioinvasive", "Follicular thyroid carcinoma (FTC), encapsulated angioinvasive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Follicular Carcinoma, Encapsulated Angioinvasive", "shortest_name_length": 31}
{"curie": "UMLS:C0338334", "names": ["recurrent pediatric supratentorial PNET", "recurrent childhood supratentorial PNET", "pediatric supratentorial PNET, recurrent", "PNET, recurrent pediatric supratentorial", "recurrent PNET, pediatric supratentorial", "recurrent PNET, childhood supratentorial", "PNET, recurrent childhood supratentorial", "childhood supratentorial PNET, recurrent", "PNET, supratentorial, childhood, recurrent", "PNET, supratentorial, pediatric, recurrent", "recurrent childhood cerebral neuroblastoma", "recurrent pediatric cerebral neuroblastoma", "recurrent cerebral neuroblastoma, childhood", "childhood cerebral neuroblastoma, recurrent", "pediatric cerebral neuroblastoma, recurrent", "recurrent neuroblastoma, childhood cerebral", "recurrent neuroblastoma, pediatric cerebral", "recurrent cerebral neuroblastoma, pediatric", "cerebral neuroblastoma, recurrent, childhood", "cerebral neuroblastoma, recurrent, pediatric", "recurrent neuroblastoma, cerebral, childhood", "recurrent neuroblastoma, cerebral, pediatric", "Recurrent Supratentorial Embryonal Tumor, NOS", "Recurrent Childhood Supratentorial Embryonal Tumor, NOS", "recurrent pediatric supratentorial primitive neuroectodermal tumor", "recurrent childhood supratentorial primitive neuroectodermal tumor", "Recurrent Childhood Supratentorial Primitive Neuroectodermal Tumor", "recurrent primitive neuroectodermal tumor, childhood supratentorial", "recurrent pediatric primitive neuroectodermal tumor, supratentorial", "childhood supratentorial primitive neuroectodermal tumor, recurrent", "recurrent primitive neuroectodermal tumor, pediatric supratentorial", "recurrent pediatric supratentorial primitive neuroectodermal tumors", "recurrent supratentorial primitive neuroectodermal tumor, pediatric", "pediatric supratentorial primitive neuroectodermal tumor, recurrent", "recurrent childhood supratentorial primitive neuroectodermal tumors", "recurrent supratentorial primitive neuroectodermal tumor, childhood", "recurrent childhood primitive neuroectodermal tumor, supratentorial", "recurrent primitive neuroectodermal tumor, supratentorial, pediatric", "recurrent primitive neuroectodermal tumor, supratentorial, childhood", "recurrent neuroectodermal tumor, pediatric, primitive, supratentorial", "recurrent neuroectodermal tumor, childhood, primitive, supratentorial", "Recurrent Childhood Supratentorial Embryonal Tumor, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Supratentorial Embryonal Tumor, Not Otherwise Specified", "shortest_name_length": 39}
{"curie": "MONDO:0008485", "names": ["sebocystomatosis", "Sebocystomatosis", "STEATOCYSTOMA MULTIPLEX", "Steatocystoma Multiplex", "Multiplex Steatocystoma", "Steatocystoma multiplex", "Multiple Sebaceous Cyst", "STEATOCYSTOMA multiplex", "multiplex steatocystoma", "steatocystoma multiplex", "Sebaceous Cyst, Multiple", "Multiplex Steatocystomas", "Cyst, Multiple Sebaceous", "Steatocystoma, Multiplex", "multiple sebaceous cysts", "Multiple Sebaceous Cysts", "Steatocystoma Multiplices", "sebaceous cysts, multiple", "Steatocystomas, Multiplex", "Sebaceous Cysts, Multiple", "SEBACEOUS CYSTS, MULTIPLE", "Cysts, Multiple Sebaceous", "steatocystoma multiplex disorder", "Steatocystoma multiplex (disorder)", "steatocystoma multiplex (diagnosis)", "Hereditary epidermal polycystic disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sebocystomatosis", "shortest_name_length": 16}
{"curie": "MONDO:0043878", "names": ["atrophy hereditary optic", "optic atrophy hereditary", "hereditary optic atrophy", "Hereditary optic atrophy", "Hereditary Optic Atrophy", "atrophy, hereditary optic", "optic atrophy, hereditary", "Optic Atrophy, Hereditary", "Atrophy, Hereditary Optic", "hereditary optic atrophies", "Hereditary Optic Atrophies", "hereditary optic Atrophies", "Optic Atrophies, Hereditary", "Atrophies, Hereditary Optic", "Atrophies, hereditary optic", "Hereditary optic atrophy, NOS", "Hereditary optic atrophy (disorder)", "Hereditary optic atrophy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary optic atrophy", "shortest_name_length": 24}
{"curie": "MONDO:0001529", "names": ["PANCYTOPENIA", "pancytopenia", "Pancytopenia", "Pancytopenias", "Pancytopaenia", "pancytopenias", "bone marrow failure", "Bone Marrow Failure", "Low blood cell count", "Pancytopenia (finding)", "Pancytopenia (disorder)", "pancytopenia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancytopenia", "shortest_name_length": 12}
{"curie": "UMLS:C1333863", "names": ["Grade II PeIN", "Grade 2 Penile Intraepithelial Neoplasia", "Grade II Penile Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade II Penile Intraepithelial Neoplasia", "shortest_name_length": 13}
{"curie": "MONDO:0001212", "names": ["Otitis media;nonsuppurative", "Nonsuppurative otitis media", "nonsuppurative otitis media", "non-suppurative otitis media", "Non-suppurative otitis media", "OTITIS MEDIA, NONSUPPURATIVE", "otitis; media, nonsuppurative", "Nonsuppurative otitis media, NOS", "Unspecified nonsuppurative otitis media", "Non-suppurative otitis media (disorder)", "Nonsuppurative otitis media, unspecified", "non-suppurative otitis media (diagnosis)", "Unspecified nonsuppurative otitis media, unspecified ear", "Nonsuppurative otitis media, not specified as acute or chronic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-suppurative otitis media", "shortest_name_length": 27}
{"curie": "UMLS:C3274453", "names": ["Acquired Cataract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired Cataract", "shortest_name_length": 17}
{"curie": "MONDO:0019187", "names": ["Rieger", "rieger anomaly", "Rieger anomaly", "Rieger Syndrome", "anomaly; Rieger", "rieger syndrome", "Rieger; anomaly", "Rieger syndrome", "riegers syndrome", "Rieger's anomaly", "rieger's syndrome", "axenfeld syndrome", "Axenfeld syndrome", "anomaly, Rieger's", "Hagedoom syndrome", "Anomaly, Rieger's", "Rieger's syndrome", "axenfelds syndrome", "Rieger malformation", "axenfeld's syndrome", "RGS - Rieger syndrome", "Rieger syndrome (RGS)", "iridodental dysplasia", "Axenfeld-Rieger syndrome", "Axenfeldt-Rieger syndrome", "Axenfeldt-Rieger Syndrome", "goniodysgenesis hypodontia", "Rieger syndrome (disorder)", "Rieger's anomaly (diagnosis)", "dysplasia marginalis posterior", "dysgenesis mesostromalis anterior", "iridocorneal mesodermal dysgenesis", "Axenfeld-Rieger syndrome (disorder)", "Axenfeld-Rieger syndrome (diagnosis)", "dysgenesis mesodermalis corneae et iridis", "mesodermal dysgenesis of anterior segment", "Iridogoniodysgenesis with somatic anomalies", "iridogoniodysgenesis with somatic anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Axenfeld-Rieger syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C1334223", "names": ["Intermediate Risk Small Intestinal GIST", "Intermediate Risk Small Intestinal Gastrointestinal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intermediate Risk Small Intestinal Gastrointestinal Stromal Tumor", "shortest_name_length": 39}
{"curie": "UMLS:C1519934", "names": ["Undifferentiated Vaginal Cancer", "Vaginal Undifferentiated Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Undifferentiated Carcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C4086156", "names": ["Childhood Embryonal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Embryonal Carcinoma", "shortest_name_length": 29}
{"curie": "UMLS:C1332283", "names": ["Anaplastic Large Cell Lymphoma, Lymphomatoid Papulosis-Like Histology"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anaplastic Large Cell Lymphoma, Lymphomatoid Papulosis-Like Histology", "shortest_name_length": 69}
{"curie": "MONDO:0003636", "names": ["Vulvar Sebaceous Carcinoma", "vulvar sebaceous carcinoma", "mammalian vulva sebaceous adenocarcinoma", "sebaceous adenocarcinoma of mammalian vulva"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar sebaceous carcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0010084", "names": ["sucrosuria, hiatus hernia and mental retardation", "Sucrosuria, Hiatus Hernia and Mental Retardation", "SUCROSURIA, HIATUS HERNIA, AND MENTAL RETARDATION", "sucrosuria, hiatus hernia and intellectual disability", "SUCROSURIA, HIATUS HERNIA, AND IMPAIRED INTELLECTUAL DEVELOPMENT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sucrosuria, hiatus hernia and intellectual disability", "shortest_name_length": 48}
{"curie": "MONDO:0700086", "names": ["UPD", "Uniparental Disomy", "Uniparental disomy", "uniparental disomy", "Disomy, Uniparental", "Uniparental Disomies", "Disomies, Uniparental", "Uniparental disomy (disorder)", "uniparental disomy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uniparental disomy", "shortest_name_length": 3}
{"curie": "MONDO:0006187", "names": ["duodenum adenoma", "duodenum villous adenoma", "duodenal villous adenoma", "Duodenal Villous Adenoma", "villous adenoma, duodenum", "Villous Adenoma, Duodenum", "Villous Adenoma of Duodenum", "villous adenoma of duodenum", "Villous adenoma of duodenum", "Villous Adenoma of the Duodenum", "villous adenoma of the duodenum", "Villous adenoma of duodenum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "duodenal villous adenoma", "shortest_name_length": 16}
{"curie": "MONDO:0035153", "names": ["Acephalic spermatozoa syndrome", "acephalic spermatozoa syndrome", "male infertility due to acephalic spermatozoa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "male infertility due to acephalic spermatozoa", "shortest_name_length": 30}
{"curie": "MONDO:0014375", "names": ["DIAR7", "diarrhea 7", "diarrhea type 7", "DGAT1 congenital diarrhea", "DIARRHEA 7, PROTEIN-LOSING ENTEROPATHY TYPE", "diarrhea 7, protein-losing enteropathy type", "congenital diarrhea caused by mutation in DGAT1", "congenital diarrhea 7 with exudative enteropathy", "congenital diarrhoea 7 with exudative enteropathy", "congenital chronic diarrhea with exudative enteropathy", "congenital chronic diarrhoea with exudative enteropathy", "congenital chronic diarrhea with protein-losing enteropathy", "congenital chronic diarrhoea with protein-losing enteropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital diarrhea 7 with exudative enteropathy", "shortest_name_length": 5}
{"curie": "MONDO:0019826", "names": ["abnormal origin or aberrant course of coronary artery"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "abnormal origin or aberrant course of coronary artery", "shortest_name_length": 53}
{"curie": "MONDO:0041261", "names": ["Acid-base balance disorder", "disorder; acid-base balance", "acid-base balance; disorder", "ACID-BASE BALANCE DISORDERS", "Disease of acid base balance", "Disorder of acid-base balance", "Diseases of Acid Base Balance", "disorder of acid-base balance", "disturbance; acid-base balance", "Disturbance of acid-base balance", "disturbance of acid-base balance", "Disorder of acid-base balance, NOS", "Disturbance of acid-base balance, NOS", "Disorder of acid-base balance (disorder)", "disorder of acid-base balance (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of acid-base balance", "shortest_name_length": 26}
{"curie": "MONDO:0014030", "names": ["CILD20", "primary ciliary dyskinesia 20", "CILIARY DYSKINESIA, PRIMARY, 20", "ciliary dyskinesia, primary, 20", "primary ciliary dyskinesia type 20", "CCDC114 primary ciliary dyskinesia", "ciliary dyskinesia, primary, type 20", "primary ciliary dyskinesia caused by mutation in CCDC114", "primary ciliary dyskinesia 20 with or without situs inversus", "CILIARY DYSKINESIA, PRIMARY, 20, WITH OR WITHOUT SITUS INVERSUS", "ciliary dyskinesia, primary, 20, with or without situs inversus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia 20", "shortest_name_length": 6}
{"curie": "MONDO:0002139", "names": ["Sigmoid Disease", "sigmoid disease", "Sigmoid Diseases", "Disease, Sigmoid", "diseases sigmoid", "Diseases, Sigmoid", "sigmoid colon disease", "Sigmoid Colon Disease", "Sigmoid Colon Diseases", "Disease, Sigmoid Colon", "Colon Disease, Sigmoid", "Diseases, Sigmoid Colon", "Colon Diseases, Sigmoid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sigmoid disease", "shortest_name_length": 15}
{"curie": "UMLS:C4527334", "names": ["Recurrent Intravascular B-Cell Lymphoma", "Recurrent Intravascular Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Intravascular Large B-Cell Lymphoma", "shortest_name_length": 39}
{"curie": "UMLS:C0936254", "names": ["polyradiculoneuritis", "Polyradiculoneuritis", "Polyradiculoneuritides"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Polyradiculoneuritis", "shortest_name_length": 20}
{"curie": "MONDO:0012431", "names": ["DIH3", "DIAPHRAGMATIC HERNIA 3", "Diaphragmatic Hernia 3", "diaphragmatic hernia 3", "diaphragmatic hernia type 3", "ZFPM2 congenital diaphragmatic hernia", "congenital diaphragmatic hernia caused by mutation in ZFPM2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diaphragmatic hernia 3", "shortest_name_length": 4}
{"curie": "MONDO:0002379", "names": ["Cystic teratoma", "cystic teratoma", "Cystic Teratoma", "Cystic teratoma, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cystic teratoma", "shortest_name_length": 15}
{"curie": "UMLS:C0266493", "names": ["Ecchordosis physaliphora", "Ecchordosis Physaliphora", "Heterotopic notochordal tissue", "Ecchordosis physaliphora (disorder)", "Ecchordosis physaliphora (diagnosis)", "ectopic neuronal tissue ecchordosis physaliphora"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ecchordosis physaliphora", "shortest_name_length": 24}
{"curie": "MONDO:0012859", "names": ["OPTB7", "TNFRSF11A osteopetrosis (disease)", "osteopetrosis autosomal recessive 7", "autosomal recessive osteopetrosis 7", "OSTEOPETROSIS, AUTOSOMAL RECESSIVE 7", "Osteopetrosis, Autosomal Recessive 7", "osteopetrosis, autosomal recessive 7", "autosomal recessive osteopetrosis type 7", "osteopetrosis, autosomal recessive type 7", "osteopetrosis-hypogammaglobulinemia syndrome", "osteopetrosis (disease) caused by mutation in TNFRSF11A", "osteopetrosis osteoclast-poor with hypogammaglobulinemia", "osteoclast-poor osteopetrosis with hypogammaglobulinemia", "Osteopetrosis, Osteoclast-Poor, With Hypogammaglobulinemia", "osteopetrosis, osteoclast-poor, with hypogammaglobulinemia", "OSTEOPETROSIS, OSTEOCLAST-POOR, WITH HYPOGAMMAGLOBULINEMIA", "autosomal recessive osteoclast-poor osteopetrosis with hypogammaglobulinemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive osteopetrosis 7", "shortest_name_length": 5}
{"curie": "MONDO:0010192", "names": ["Ws4", "WS4", "WS4A", "Waardenburg Shah syndrome", "Shah Waardenburg syndrome", "Waardenburg-Shah syndrome", "Waardenburg-Shah Syndrome", "Shah-Waardenburg syndrome", "WAARDENBURG-SHAH SYNDROME", "SHAH-WAARDENBURG SYNDROME", "EDNRB Waardenburg syndrome", "Waardenburg syndrome type 4", "Waardenburg Syndrome Type 4", "Waardenburg syndrome type 4A", "Waardenburg syndrome type IV", "Waardenburg syndrome, type 4", "Waardenburg Syndrome Type IV", "Waardenburg Syndrome, Type 4a", "WAARDENBURG SYNDROME, TYPE 4A", "Waardenburg syndrome, type 4A", "Waardenburg syndrome type IVA", "WAARDENBURG SYNDROME, TYPE IVA", "Waardenburg Syndrome, Type Iva", "Waardenburg-Hirschsprung disease", "Waardenburg Hirschsprung syndrome", "Waardenburg-Hirschsprung syndrome", "Waardenburg Shah syndrome (disorder)", "Waardenburg syndrome type IV (diagnosis)", "Hirschsprung disease with pigmentary anomaly", "Waardenburg syndrome caused by mutation in EDNRB", "Waardenburg syndrome with Hirschsprung disease type 4A", "Waardenburg syndrome with Hirschsprung disease, type 4A", "WAARDENBURG SYNDROME WITH HIRSCHSPRUNG DISEASE, TYPE 4A", "Waardenburg Syndrome With Hirschsprung Disease, Type 4a", "Waardenburg syndrome co-occurrent with Hirschsprung disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Waardenburg syndrome type 4A", "shortest_name_length": 3}
{"curie": "UMLS:C1332059", "names": ["AIDS-Related Primary Effusion Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Primary Effusion Lymphoma", "shortest_name_length": 38}
{"curie": "MONDO:0017031", "names": ["primary ILD in childhood and adulthood", "primary interstitial lung disease in childhood and adulthood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary interstitial lung disease in childhood and adulthood", "shortest_name_length": 38}
{"curie": "MONDO:0001689", "names": ["tongue papillae hypertrophy", "tongue papillary hypertrophy", "hypertrophy; tongue papillae", "tongue papillae; hypertrophy", "Tongue papillary hypertrophy", "Hypertrophy of tongue papillae", "hypertrophy of tongue papillae", "hypertrophy of lingual papillae", "Tongue papillary hypertrophy NOS", "Hypertrophy of tongue papillae (disorder)", "hypertrophy of lingual papillae (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophy of tongue papillae", "shortest_name_length": 27}
{"curie": "MONDO:0004501", "names": ["Fallopian Tube Cystadenofibroma", "fallopian tube cystadenofibroma", "Cystadenofibroma of fallopian tube", "cystadenofibroma of fallopian tube", "fallopian tube serous cystadenofibroma", "Fallopian Tube Serous Cystadenofibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fallopian tube cystadenofibroma", "shortest_name_length": 31}
{"curie": "UMLS:C4551539", "names": ["stage I vaginal cancer", "Stage I Vaginal Cancer", "Vaginal Cancer Stage I", "AJCC Stage I Vaginal Cancer", "FIGO Stage I Vagina Carcinoma", "Stage I Vaginal Cancer AJCC v6", "Stage I Vaginal Cancer AJCC v7", "FIGO Stage I Vaginal Carcinoma", "FIGO Stage I Carcinoma of Vagina", "Stage I Vaginal Carcinoma AJCC v7", "Stage I Vaginal Carcinoma AJCC v6", "FIGO Stage I Carcinoma of the Vagina", "Stage I Vaginal Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Vaginal Cancer AJCC v6 and v7", "shortest_name_length": 22}
{"curie": "MONDO:0014878", "names": ["PDA2", "patent ductus arteriosus 2", "PATENT DUCTUS ARTERIOSUS 2", "patent ductus arteriosus type 2", "patent ductus arteriosus 2; PDA2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "patent ductus arteriosus 2", "shortest_name_length": 4}
{"curie": "MONDO:0000984", "names": ["thalassemia", "Thalassemia", "THALASSEMIA", "Thalassemias", "THALASSEMIAS", "thalassemias", "thalassaemia", "Thalassaemia", "thalassaemias", "Thalassemia NOS", "Thalassaemia NOS", "Thalassemia, NOS", "anemia; thalassemia", "thalassemia; anemia", "Thalassemic syndrome", "Thalassemia syndrome", "thalassemia disorder", "Thalassaemia syndrome", "syndromes thalassemia", "Thalassemic Syndromes", "Thalassaemic disorders", "Thalassemia (disorder)", "thalassemia (diagnosis)", "Hereditary leptocytosis", "Thalassemia, unspecified", "leptocytosis; hereditary", "Thalassaemia, unspecified", "Thalassemia syndrome, NOS", "Thalassemia syndrome (disorder)", "thalassemia; disorder, hemoglobin", "hemoglobinopathy; with thalassemia", "sickle-cell thalassemia with crisis", "Sickle-cell thalassemia with crisis", "thalassemia Hb-S disease with crisis", "hypochromic / microcytic thalassemia", "Sickle-cell thalassemia without crisis", "sickle-cell thalassemia without crisis", "thalassemia Hb-S disease without crisis", "hypochromic / microcytic thalassemia anemia", "hypochromic / microcytic thalassemia (diagnosis)", "thalassemia; hemoglobinopathy (with thalassemia)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thalassemia", "shortest_name_length": 11}
{"curie": "UMLS:C0406716", "names": ["Hypodontia and nail dysgenesis", "Hypodontia and nail dysgenesis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypodontia and nail dysgenesis", "shortest_name_length": 30}
{"curie": "MONDO:0005625", "names": ["Cerebral malaria", "cerebral malaria", "CEREBRAL MALARIA", "Cerebral Malaria", "Malaria, cerebral", "Malaria, Cerebral", "Cerebral malaria NOS", "malarial encephalitis", "Malarial encephalitis", "Cerebral malaria (disorder)", "cerebral malaria (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral malaria", "shortest_name_length": 16}
{"curie": "MONDO:0006884", "names": ["Panophthalmitis", "panophthalmitis", "PANOPHTHALMITIS", "Panophthalmitides", "Entire eye inflamed", "Panophthalmitis (disorder)", "Inflammation of entire eye", "panophthalmitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "panophthalmitis", "shortest_name_length": 15}
{"curie": "UMLS:C0279629", "names": ["adult acute M5a leukemia", "M5a Adult Acute Leukemia", "Adult Acute M5a Leukemia", "M5a leukemia, adult acute", "Acute Monoblastic Leukemia", "Adult Acute Monoblastic Leukemia", "acute monoblastic leukemia, adult", "leukemia, adult acute monoblastic", "monoblastic leukemia, adult acute", "adult acute monoblastic leukemia (M5a)", "adult acute poorly differentiated monoblastic leukemia", "M5a adult acute poorly differentiated monocytic leukemia", "M5a Adult Acute Poorly Differentiated Monoblastic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Acute Monoblastic Leukemia", "shortest_name_length": 24}
{"curie": "UMLS:C0015408", "names": ["eye trauma", "Injury;eye", "Injury-eye", "Eye Injury", "Eye injury", "EYE INJURY", "eye injury", "injury; eye", "eye; injury", "Injury, Eye", "Eye Injuries", "eye injuries", "Eye injuries", "Injury of eye", "Injuries, Eye", "Ocular Injury", "Ocular injury", "ocular; wound", "ocular injury", "wound; ocular", "Eye injury NOS", "injuries of eye", "ocular injuries", "Ocular injuries", "Injury of eye NOS", "Injury of eye, NOS", "Injury of Eye Region", "eye injury (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eye Injuries", "shortest_name_length": 10}
{"curie": "UMLS:C0521476", "names": ["Infected nail bed", "nail bed infection", "Nail bed infection", "infection nail bed", "Nail bed infection NOS", "Nail bed infection (disorder)", "Nail bed infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nail bed infection", "shortest_name_length": 17}
{"curie": "UMLS:C5237385", "names": ["Refractory Breast Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Breast Adenocarcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0020039", "names": ["46,XX DSD induced by androgens excess", "46,XX disorder of sex development induced by androgens excess"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XX disorder of sex development induced by androgens excess", "shortest_name_length": 37}
{"curie": "UMLS:C0752262", "names": ["Somatosensory Disorder", "Somatosensory Disorders", "Somatic Sensation Disorder", "Sensation Disorder, Somatic", "Somatic Sensation Disorders", "Sensation Disorders, Somatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Somatosensory Disorders", "shortest_name_length": 22}
{"curie": "MONDO:0013244", "names": ["BDE2", "brachydactyly type E2", "BRACHYDACTYLY, TYPE E2", "brachydactyly, type E2", "PTHLH brachydactyly type E", "brachydactyly type E caused by mutation in PTHLH"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly type E2", "shortest_name_length": 4}
{"curie": "MONDO:0001742", "names": ["Subacute closed-angle glaucoma", "Interval angle-closure glaucoma", "Subacute angle-closure glaucoma", "interval angle-closure glaucoma", "Prodromal angle closure glaucoma", "Angle-closure glaucoma, subacute", "angle-closure glaucoma, subacute", "prodromal angle closure glaucoma", "Angle-closure glaucoma, interval", "Intermittent closed-angle glaucoma", "intermittent angle-closure glaucoma", "Intermittent angle-closure glaucoma", "interval primary angle-closure glaucoma", "intermittent primary angle-closure glaucoma", "Intermittent angle-closure glaucoma (disorder)", "interval primary angle-closure glaucoma (diagnosis)", "intermittent primary angle-closure glaucoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "interval angle-closure glaucoma", "shortest_name_length": 30}
{"curie": "UMLS:C4316812", "names": ["Hypofibrinogenemia", "DEFICIENCY FACTOR I", "Deficiency factor I", "factor i deficiency", "Factor I Deficiency", "Factor I deficiency", "Deficiency, factor I", "Fibrinogen deficiency", "Fibrinogen Deficiency", "fibrinogen; deficiency", "deficiency; fibrinogen", "Deficiency, Fibrinogen", "Deficiency, fibrinogen", "Fibrinogen Deficiencies", "Fibrinogen deficiency (disorder)", "Deficiency of factor I [fibrinogen]", "congenital factor I (fibrinogen) deficiency", "congenital factor I (fibrinogen) deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fibrinogen Deficiency", "shortest_name_length": 18}
{"curie": "UMLS:C4683008", "names": ["Eyelid Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eyelid Carcinoma by AJCC v7 Stage", "shortest_name_length": 33}
{"curie": "MONDO:0013260", "names": ["EOE2", "esophagitis, eosinophilic, 2", "ESOPHAGITIS, EOSINOPHILIC, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophagitis, eosinophilic, 2", "shortest_name_length": 4}
{"curie": "MONDO:0036501", "names": ["resistant cancer", "Refractory cancer", "Refractory Cancer", "cancer refractory", "refractory cancer", "clinical resistance", "Refractory Malignant Neoplasm", "refractory malignant neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "refractory malignant neoplasm", "shortest_name_length": 16}
{"curie": "MONDO:0014569", "names": ["LCCS7", "LETHAL CONGENITAL CONTRACTURE SYNDROME 7", "lethal congenital contracture syndrome 7", "lethal congenital contracture syndrome type 7", "CNTNAP1 lethal congenital contracture syndrome", "lethal congenital contracture syndrome caused by mutation in CNTNAP1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal congenital contracture syndrome 7", "shortest_name_length": 5}
{"curie": "UMLS:C5555560", "names": ["Borderline Ovarian Seromucinous Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Ovarian Seromucinous Tumor", "shortest_name_length": 37}
{"curie": "MONDO:0043349", "names": ["Masson Lesion", "Masson lesion", "Masson's tumor", "Masson Hemangioma", "Masson Pseudotumor", "Masson pseudotumor", "Masson's Pseudotumor", "Masson's pseudotumor", "Masson's pseudosarcoma", "Masson's Pseudosarcoma", "masson's pseudosarcoma", "Masson's pseudoangiosarcoma", "Masson's Vegetant Hemangioma", "Masson's vegetant hemangioma", "Papillary Endothelial Hyperplasia", "papillary endothelial hyperplasia", "Intravascular papillary endothelial hyperplasia", "Intravascular Papillary Endothelial Hyperplasia", "intravascular papillary endothelial hyperplasia", "Masson's vegetant intravascular hemangio-endothelioma", "Intravascular papillary endothelial hyperplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intravascular papillary endothelial hyperplasia", "shortest_name_length": 13}
{"curie": "UMLS:C1333053", "names": ["Ciliary Body Spindle Cell Type A Melanoma", "Spindle Cell Type A Melanoma of Ciliary Body", "Spindle Cell Type A Melanoma of the Ciliary Body"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ciliary Body Spindle Cell Type A Melanoma", "shortest_name_length": 41}
{"curie": "UMLS:C4744558", "names": ["Metastatic Lip Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Lip Carcinoma", "shortest_name_length": 24}
{"curie": "UMLS:C1336812", "names": ["Transplant-Related Kaposi Sarcoma", "Transplant-Related Kaposi's Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transplant-Related Kaposi Sarcoma", "shortest_name_length": 33}
{"curie": "UMLS:C1335349", "names": ["Parathyroid chief-cell hyperplasia", "Parathyroid Chief Cell Hyperplasia", "Chief Cell Hyperplasia of Parathyroid", "Chief Cell Hyperplasia of the Parathyroid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parathyroid chief-cell hyperplasia", "shortest_name_length": 34}
{"curie": "UMLS:C4553579", "names": ["stage III ureter cancer", "Stage III Ureter Cancer", "Stage III Ureter Cancer AJCC v8", "stage III ureter cancer AJCC v8", "Stage III Ureter Urothelial Carcinoma AJCC v8", "stage III ureter urothelial carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Ureter Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "MONDO:0023226", "names": ["gershinibaruch Leibo syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gershinibaruch Leibo syndrome", "shortest_name_length": 29}
{"curie": "MONDO:0018950", "names": ["MCCD", "MCC1D", "MCCD TYPE 1", "MCCD Type 1", "MCC deficiency", "Mcc Deficiency", "3MCC deficiency", "BMCC deficiency", "MCC1 Deficiency", "MCC1 DEFICIENCY", "Bmcc Deficiency", "3-MCC deficiency", "3-MCC Deficiency", "3-Mcc Deficiency", "methylcrotonylglycinuria", "3 Methylcrotonylglycinuria", "3-methylcrotonylglycinuria", "3-Methylcrotonylglycinuria", "3-METHYLCROTONYLGLYCINURIA I", "3-Methylcrotonylglycinuria I", "Methylcrotonylglycinuria Type I", "METHYLCROTONYLGLYCINURIA TYPE I", "3 alpha methylcrotonylglycinuria 1", "3-Methylcrotonylglycinuria, type 1", "beta-Methylcrotonylglycinuria, type 1", "Methylcrotonyl-Coa Carboxylase Deficiency", "Methylcrotonyl-CoA Carboxylase Deficiency", "Methylcrotonyl-CoA carboxylase deficiency", "3-Methylcrotonyl-CoA Carboxylase Deficiency", "3-Methylcrotonyl-CoA carboxylase deficiency", "3-Methylcrotonyl-Coa Carboxylase Deficiency", "3-methylcrotonyl-CoA carboxylase deficiency", "3 Methylcrotonyl-CoA carboxylase deficiency", "methylcrotonoyl-CoA carboxylase 1 deficiency", "Deficiency of Methylcrotonoyl-Coa Carboxylase", "3-methylcrotonyl CoA carboxylase 1 deficiency", "3-METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY", "3-@METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY", "Methylcrotonyl-coenzyme A carboxylase deficiency", "3-Methylcrotonyl-Coenzyme A Carboxylase Deficiency", "3-methylcrotonyl-CoA carboxylase deficiency (diagnosis)", "Methylcrotonyl-coenzyme A carboxylase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "3-methylcrotonyl-CoA carboxylase deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0006387", "names": ["Lung Diffuse Large B-Cell Lymphoma", "lung diffuse large B-cell lymphoma", "High Grade MALT Lymphoma of the Lung", "high grade MALT lymphoma of the lung", "large B-cell diffuse lymphoma of lung", "diffuse large B-cell lymphoma of lung", "pulmonary diffuse large B-cell lymphoma", "Pulmonary Diffuse Large B-Cell Lymphoma", "Primary Lung Diffuse Large B-Cell Lymphoma", "primary pulmonary diffuse large B-cell lymphoma", "Primary Pulmonary Diffuse Large B-Cell Lymphoma", "large B-cell diffuse lymphoma of lung (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary pulmonary diffuse large B-cell lymphoma", "shortest_name_length": 34}
{"curie": "MONDO:0021353", "names": ["uterus tumor", "tumor uterus", "Uterine Tumor", "Uterine tumor", "tumors uterus", "tumour uterus", "uterine tumor", "uterus; tumor", "Uterine tumour", "Uterine cancer", "Uterus--Tumors", "Tumor of Uterus", "Uterus Neoplasm", "tumor of uterus", "Tumor of uterus", "of uterus tumor", "neoplasm uterus", "uterus neoplasm", "uterine neoplasm", "Tumour of uterus", "neoplasms uterus", "UTERINE NEOPLASM", "NEOPLASM UTERINE", "Uterine neoplasm", "Uterus Neoplasms", "Uterine Neoplasm", "Neoplasm uterine", "tumour of uterus", "Neoplasm, Uterus", "Uterine neoplasia", "Uterine neoplasms", "uterine neoplasms", "Neoplasm, Uterine", "Uterine Neoplasms", "Neoplasms, Uterus", "Neoplasm of Uterus", "neoplasm of uterus", "Neoplasms, Uterine", "Neoplasm of uterus", "Tumor of the Uterus", "tumor of the uterus", "Uterine neoplasm NOS", "Neoplasm of the Uterus", "neoplasm of the uterus", "uterus neoplasm (disease)", "Neoplasm of uterus (disorder)", "neoplasm of uterus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tumor of uterus", "shortest_name_length": 12}
{"curie": "MONDO:0044996", "names": ["cerebral cortex disease", "cerebral cortex disorder", "disease of cerebral cortex", "Disease of cerebral cortex", "Disorder of cerebral cortex", "disorder of cerebral cortex", "disorder of brain cerebral cortex", "cerebral cortex disease or disorder", "Disorder of cerebral cortex (disorder)", "disease or disorder of cerebral cortex", "Disorder of cerebral cortex (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral cortex disorder", "shortest_name_length": 23}
{"curie": "MONDO:0009105", "names": ["THES", "THES1", "SD/THE", "THE SYNDROME", "Syndromic diarrhea", "syndromic diarrhea", "Syndromic diarrhoea", "Phenotypic diarrhea", "phenotypic diarrhea", "Diarrhea, Syndromic", "DIARRHEA, SYNDROMIC", "Syndromatic diarrhea", "Trichohepatoenteric Syndrome", "Trichohepatoenteric syndrome", "trichohepatoenteric syndrome", "Tricho-hepato-enteric syndrome", "Phenotypic diarrhea of infancy", "Phenotypic diarrhoea of infancy", "Trichohepatoenteric syndrome type 1", "Trichohepatoenteric syndrome (disorder)", "Intractable diarrhea with phenotypic anomalies", "Intractable diarrhoea with phenotypic anomalies", "syndromic diarrhea/Tricho-hepato-enteric syndrome", "Syndromic diarrhea/Tricho-hepato-enteric syndrome", "Fatal infantile diarrhea with trichorrhexis nodosa", "Fatal infantile diarrhoea with trichorrhexis nodosa", "DIARRHEA, FATAL INFANTILE, WITH TRICHORRHEXIS NODOSA", "Diarrhea, Fatal Infantile, with Trichorrhexis Nodosa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichohepatoenteric syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0016844", "names": ["Dup(20p)", "dup(20p)", "trisomy 20p", "20p trisomy", "Trisomy 20p", "Duplication 20p", "20p duplication", "trisomy type 20p", "Duplication of 20p", "partial trisomy 20p", "Trisomy 20p syndrome", "chromosome 20p duplication", "20p partial trisomy syndrome", "Chromosome 20, duplication 20p", "partial trisomy of chromosome 20p", "Partial trisomy of chromosome 20p", "partial duplication of chromosome 20p", "Partial duplication of chromosome 20p", "20p partial trisomy syndrome (disorder)", "Partial trisomy of the short arm of chromosome 20", "partial trisomy of the short arm of chromosome 20", "Partial duplication of the short arm of chromosome 20", "partial duplication of the short arm of chromosome 20"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trisomy 20p", "shortest_name_length": 8}
{"curie": "MONDO:0006662", "names": ["MENINGITIS ASEPTIC", "ASEPTIC MENINGITIS", "Aseptic Meningitis", "aseptic meningitis", "meningitis aseptic", "Aseptic meningitis", "Meningitis aseptic", "aseptic; meningitis", "meningitis; aseptic", "MENINGITIS, ASEPTIC", "Meningitis, Aseptic", "acute aseptic meningitis", "Aseptic meningitis (disorder)", "aseptic meningitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aseptic meningitis", "shortest_name_length": 18}
{"curie": "MONDO:0014332", "names": ["CA5AD", "CA-VA deficiency", "Carbonic anhydrase VA deficiency", "carbonic anhydrase VA deficiency", "CA-VA (carbonic anhydrase VA) deficiency", "mitochondrial carbonic anhydrase va deficiency", "hyperammonemia due to carbonic anhydrase VA deficiency", "CARBONIC ANHYDRASE VA DEFICIENCY, HYPERAMMONEMIA DUE TO", "carbonic anhydrase 5A deficiency, hyperammonemia due to", "carbonic anhydrase VA deficiency, hyperammonemia due to", "hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency", "Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency", "toxic encephalopathy hyperammonemic due to carbonic anhydrase va deficiency", "Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency (disorder)", "Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C5419075", "names": ["Locally Advanced Ocular Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Ocular Melanoma", "shortest_name_length": 32}
{"curie": "MONDO:0016348", "names": ["non-genetic cardiac rhythm disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-genetic cardiac rhythm disease", "shortest_name_length": 34}
{"curie": "MONDO:0011151", "names": ["Evr4", "EVR4", "Exudative Vitreoretinopathy 4", "exudative vitreoretinopathy 4", "EXUDATIVE VITREORETINOPATHY 4", "exudative vitreoretinopathy type 4", "EXUDATIVE VITREORETINOPATHY 4 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exudative vitreoretinopathy 4", "shortest_name_length": 4}
{"curie": "MONDO:0012488", "names": ["HBV, resistance to", "HBV, RESISTANCE TO", "HBV, SUSCEPTIBILITY TO", "HBV, susceptibility to", "Hepatitis B Virus, resistance to", "HEPATITIS B VIRUS, RESISTANCE TO", "HEPATITIS B VIRUS, SUSCEPTIBILITY TO", "hepatitis B virus, susceptibility to", "hepatitis b virus, susceptibility to", "hepatitis B virus infection, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatitis B virus, susceptibility to", "shortest_name_length": 18}
{"curie": "UMLS:C1708602", "names": ["Head and Neck Keratinizing Squamous Cell Carcinoma", "Keratinizing Head and Neck Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Head and Neck Keratinizing Squamous Cell Carcinoma", "shortest_name_length": 50}
{"curie": "UMLS:C4744365", "names": ["Sellar Paraganglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sellar Paraganglioma", "shortest_name_length": 20}
{"curie": "MONDO:0013492", "names": ["APMR3", "alopecia-mental retardation syndrome 3", "ALOPECIA-MENTAL RETARDATION SYNDROME 3", "ALOPECIA-INTELLECTUAL DISABILITY SYNDROME 3", "alopecia-intellectual disability syndrome 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alopecia-intellectual disability syndrome 3", "shortest_name_length": 5}
{"curie": "MONDO:0010771", "names": ["CSH", "myocardial hamartoma", "Myocardial Hamartoma", "Purkinje Cell Hamartoma", "Purkinje cell hamartoma", "Oncocytic Cardiomyopathy", "oncocytic cardiomyopathy", "Oncocytic cardiomyopathy", "CARDIOMYOPATHY, ONCOCYTIC", "cardiomyopathy, oncocytic", "Congenital Cardiomyopathy", "congenital cardiomyopathy", "Cardiomyopathy, Oncocytic", "Isolated cardiac lipidosis", "focal lipid cardiomyopathy", "isolated Cardiac lipidosis", "Focal lipid cardiomyopathy", "Isolated Cardiac Lipidosis", "CARDIOMYOPATHY, FOCAL LIPID", "Conduction System Hamartoma", "Histiocytoid cardiomyopathy", "histiocytoid cardiomyopathy", "cardiomyopathy, focal Lipid", "Cardiomyopathy, Focal Lipid", "Histiocytoid Cardiomyopathy", "Cardiomyopathy, histiocytoid", "Foamy myocardial transformation", "Arachnocytosis of the myocardium", "Arachnocytosis of the Myocardium", "Infantile xanthomatous cardiomyopathy", "infantile histiocytoid cardiomyopathy", "infantile xanthomatous cardiomyopathy", "Infantile Xanthomatous Cardiomyopathy", "Cardiomyopathy, infantile histiocytoid", "CARDIOMYOPATHY, INFANTILE HISTIOCYTOID", "Cardiomyopathy, Infantile Xanthomatous", "CARDIOMYOPATHY, INFANTILE XANTHOMATOUS", "cardiomyopathy, infantile xanthomatous", "cardiomyopathy, infantile histiocytoid", "Myocardial or conduction system hamartoma", "Foamy myocardial transformation of infancy", "foamy myocardial transformation of infancy", "FOAMY MYOCARDIAL TRANSFORMATION OF INFANCY", "Infantile cardiomyopathy with histiocytoid change", "infantile cardiomyopathy with histiocytoid change", "Infantile cardiomyopathy with histiocytoid changes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "histiocytoid cardiomyopathy", "shortest_name_length": 3}
{"curie": "MONDO:0023370", "names": ["neoplastic disease", "neoplastic disorder", "neoplastic disease or syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplastic disease or syndrome", "shortest_name_length": 18}
{"curie": "UMLS:C4726591", "names": ["Acute Leukemia of Ambiguous Lineage, NOS", "Acute Leukemia of Ambiguous Lineage, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Leukemia of Ambiguous Lineage, Not Otherwise Specified", "shortest_name_length": 40}
{"curie": "UMLS:C1274988", "names": ["Drug-induced mucositis", "Drug-induced mucositis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drug-induced mucositis", "shortest_name_length": 22}
{"curie": "MONDO:0017736", "names": ["disorder of sialic acid metabolism", "Disorder of sialic acid metabolism", "Disorder of sialic acid metabolism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of sialic acid metabolism", "shortest_name_length": 34}
{"curie": "UMLS:C1336266", "names": ["Stage III Renal Pelvis Cancer", "Stage III Renal Pelvis Carcinoma", "Stage III Carcinoma of Renal Pelvis", "Stage III Renal Pelvis Cancer AJCC v7", "Stage III Carcinoma of the Renal Pelvis", "Stage III Renal Pelvis Carcinoma AJCC v7", "Stage III Renal Pelvis Carcinoma AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Renal Pelvis Cancer AJCC v7", "shortest_name_length": 29}
{"curie": "MONDO:0013334", "names": ["COCOON SYNDROME", "Cocoon syndrome", "cocoon syndrome", "fetal encasement syndrome", "Fetal encasement syndrome", "FETAL ENCASEMENT SYNDROME", "Foetal encasement syndrome", "Fetal encasement syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cocoon syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0014559", "names": ["MRT48", "mental retardation, autosomal recessive 48", "intellectual disability, autosomal recessive 48", "mental retardation, autosomal recessive type 48", "intellectual disability, autosomal recessive type 48", "autosomal recessive intellectual developmental disorder 48", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 48", "progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome", "Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome", "Progressive essential tremor, speech impairment, facial dysmorphism, intellectual disability, abnormal behavior syndrome", "Progressive essential tremor, speech impairment, facial dysmorphism, intellectual disability, abnormal behaviour syndrome", "Progressive essential tremor, speech impairment, facial dysmorphism, intellectual disability, abnormal behavior syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C1535919", "names": ["Fetal chromosome abnormality", "Foetal chromosome abnormality"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fetal chromosome abnormality", "shortest_name_length": 28}
{"curie": "UMLS:C0234458", "names": ["Dream disorder", "Dreams abnormal", "abnormal dreams", "ABNORMAL DREAMS", "disorders dream", "Abnormal dreams", "DREAMS ABNORMAL", "Abnormal dreaming", "Dreaming abnormal", "DREAMING ABNORMAL", "Dream disorder (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dream disorder", "shortest_name_length": 14}
{"curie": "UMLS:C5238956", "names": ["Unresectable Differentiated Thyroid Gland Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Differentiated Thyroid Gland Carcinoma", "shortest_name_length": 51}
{"curie": "MONDO:0022757", "names": ["trisomy 20", "Trisomy 20", "trisomy; 20", "Mosaic trisomy 20", "mosaic trisomy 20", "Trisomy 20 mosaicism", "trisomy 20 mosaicism", "chromosome 20 trisomy", "trisomy chromosome 20", "Chromosome 20, trisomy", "chromosome; 20, trisomy", "Chromosome 20 duplication", "Mosaic trisomy 20 syndrome", "Mosaic trisomy chromosome 20", "Complete trisomy 20 syndrome", "Mosaic trisomy 20 syndrome (disorder)", "Mosaic trisomy 20 syndrome (diagnosis)", "Complete trisomy 20 syndrome (disorder)", "anomaly of chromosome mosaic trisomy 20 syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 20 trisomy", "shortest_name_length": 10}
{"curie": "MONDO:0012664", "names": ["SPAX3", "ARSAL", "spastic ataxia 3", "spastic ataxia type 3", "spastic ataxia 3, autosomal recessive", "SPASTIC ATAXIA 3, AUTOSOMAL RECESSIVE", "Ataxia, Spastic, 3, Autosomal Recessive", "MARS2 autosomal recessive spastic ataxia", "Autosomal recessive spastic ataxia type 3", "autosomal recessive spastic ataxia type 3", "SPAX3 - autosomal recessive spastic ataxia type 3", "Autosomal recessive spastic ataxia with leucoencephalopathy", "AUTOSOMAL RECESSIVE SPASTIC ATAXIA WITH LEUKOENCEPHALOPATHY", "autosomal recessive spastic ataxia with leukoencephalopathy", "Autosomal recessive spastic ataxia with leukoencephalopathy", "Autosomal Recessive Spastic Ataxia With Leukoencephalopathy", "autosomal recessive spastic ataxia caused by mutation in MARS2", "ARSAL - autosomal recessive spastic ataxia with leukoencephalopathy", "ARSAL - autosomal recessive spastic ataxia with leucoencephalopathy", "Autosomal recessive spastic ataxia with leukoencephalopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic ataxia 3", "shortest_name_length": 5}
{"curie": "UMLS:C0268969", "names": ["hemorrhage; testis", "testis; hemorrhage", "Testicular bleeding", "Hemorrhage of testis", "Testicular Hemorrhage", "Testicular hemorrhage", "Haemorrhage of testis", "hemorrhage of testicle", "Testicular haemorrhage", "Hemorrhage of testis (disorder)", "hemorrhage of testicle (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemorrhage of testis", "shortest_name_length": 18}
{"curie": "UMLS:C5234873", "names": ["Relapsed Nasopharyngeal Keratinizing Epidermoid Carcinoma", "Relapsed Keratinizing Epidermoid Carcinoma of Nasopharynx", "Recurrent Nasopharyngeal Keratinizing Epidermoid Carcinoma", "Recurrent Keratinizing Epidermoid Carcinoma of Nasopharynx", "Relapsed Nasopharyngeal Keratinizing Squamous Cell Carcinoma", "Relapsed Keratinizing Squamous Cell Carcinoma of Nasopharynx", "Relapsed Keratinizing Epidermoid Carcinoma of the Nasopharynx", "Recurrent Nasopharyngeal Keratinizing Squamous Cell Carcinoma", "Recurrent Keratinizing Squamous Cell Carcinoma of Nasopharynx", "Recurrent Keratinizing Epidermoid Carcinoma of the Nasopharynx", "Relapsed Keratinizing Squamous Cell Carcinoma of the Nasopharynx", "Recurrent Nasopharyngeal Throat Keratinizing Squamous Cell Cancer", "Recurrent Keratinizing Squamous Cell Carcinoma of the Nasopharynx"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Nasopharyngeal Keratinizing Squamous Cell Carcinoma", "shortest_name_length": 57}
{"curie": "MONDO:0023558", "names": ["Hoffman syndrome", "Myxedema myopathy", "Hoffmann syndrome", "Myxoedema myopathy", "myopathy hypothyroid", "Myopathy in myxedema", "hypothyroid myopathy", "Hypothyroid myopathy", "Debre-Semelaigne syndrome", "Débré-Sémélaigne syndrome", "myopathy-myxedema syndrome", "Débré-Sémélaigne's syndrome", "Debre-Semelaigne's syndrome", "myopathy secondary to myxedema", "Kocher Debre Semelaigne disease", "Kocher debre Semelaigne disease", "Hypothyroid myopathy (disorder)", "Kocher Debre Semelaigne syndrome", "Kocher-Debre-Semelaigne syndrome", "Kocher-debre-Semelaigne syndrome", "kocher-debre-semelaigne syndrome", "Kocher-Debré-Semelaigne syndrome", "hypothyroid-large muscle syndrome", "Pseudomyotonic myopathy, hypothyroid", "myxedema-myotonic dystrophy syndrome", "Kocher-Debre-Semelaigne (KDS) syndrome", "myxedema-muscular hypertrophy syndrome", "Débré-Sémélaigne's syndrome (disorder)", "cretinism-muscular hypertrophy syndrome", "infantile myxedema-muscular hypertrophy", "myopathy secondary to myxedema (diagnosis)", "Muscular pseudohypertrophy-hypothyroidism syndrome", "Muscular pseudohypertrophy and hypothyroidism syndrome", "Muscular pseudohypertrophy and hypothyroidism syndrome (disorder)", "association of muscular pseudohypertrophy and hypothyroidism in children"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kocher-debre-Semelaigne syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0004194", "names": ["ovarian stromal hyperthecosis", "Ovarian Stromal Hyperthecosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian stromal hyperthecosis", "shortest_name_length": 29}
{"curie": "MONDO:0005884", "names": ["Opisthorchiosis", "OPISTHORCHIASIS", "Opisthorchiases", "Opisthorchiasis", "opisthorchiasis", "Opisthorchis Infection", "Infection, Opisthorchis", "Opisthorchis Infections", "Infections, Opisthorchis", "infection by Opisthorchis", "Opisthorchis; infestation", "liver; fluke disease, cat", "Cat liver fluke infection", "fluke disease; liver, cat", "infestation; Opisthorchis", "Infection by Opisthorchis", "infection; cat liver fluke", "cat liver fluke; infection", "Opisthorchiasis (disorder)", "opisthorchiasis (diagnosis)", "Infection by cat liver fluke", "infection due to cat liver fluke", "infection due to Opisthorchis (felineus)(viverrini)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "opisthorchiasis", "shortest_name_length": 15}
{"curie": "UMLS:C5555847", "names": ["Peritoneal Sarcomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peritoneal Sarcomatosis", "shortest_name_length": 23}
{"curie": "MONDO:0011186", "names": ["USH1F", "Usher syndrome type 1F", "Usher syndrome type IF", "Usher Syndrome, Type IF", "USHER SYNDROME, TYPE IF", "Usher syndrome, type 1F", "USHER syndrome, type IF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Usher syndrome type 1F", "shortest_name_length": 5}
{"curie": "UMLS:C5447304", "names": ["Locally Recurrent Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Recurrent Disease", "shortest_name_length": 25}
{"curie": "UMLS:C1334173", "names": ["Infantile Hemangiopericytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infantile Hemangiopericytoma", "shortest_name_length": 28}
{"curie": "MONDO:0800035", "names": ["MTTK MELAS syndrome", "MELAS syndrome caused by mutation in MTTK"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MELAS syndrome caused by mutation in MTTK", "shortest_name_length": 19}
{"curie": "UMLS:C0751022", "names": ["Transient Brainstem Ischemia", "Brainstem Ischemia, Transient", "Ischemia, Transient Brainstem", "Ischemias, Transient Brainstem", "Brainstem Ischemias, Transient", "Brain Stem Ischemia, Transient", "Brainstem Transient Ischemic Attack", "Transient Ischemic Attack, Brainstem", "Brain Stem Transient Ischemic Attack", "Transient Ischemic Attack, Brain Stem"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brain Stem Ischemia, Transient", "shortest_name_length": 28}
{"curie": "MONDO:0012395", "names": ["CATC2", "CTRCT18", "CATARACT 18", "cataract 18", "cataract type 18", "FYCO1 cataract (disease)", "cataract 18 autosomal recessive", "cataract 18, autosomal recessive", "autosomal recessive congenital cataract 2", "cataract, autosomal recessive congenital 2", "Cataract, autosomal recessive congenital 2", "CATARACT, AUTOSOMAL RECESSIVE CONGENITAL 2", "cataract (disease) caused by mutation in FYCO1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 18", "shortest_name_length": 5}
{"curie": "MONDO:0005892", "names": ["OME", "glue ear", "Glue ear", "GLUE EAR", "ear glue", "ears glue", "Glue ear - mucoid", "Serous Otitis Media", "serous otitis Media", "Middle Ear Effusion", "Effusion;middle ear", "mucoid otitis media", "Mucoid otitis media", "middle ear effusion", "Effusion, Middle Ear", "Otitis media, mucoid", "Middle Ear Effusions", "Ear Effusion, Middle", "middle ear effusions", "effusion otitis media", "Ear Effusions, Middle", "otitis; media, mucoid", "Effusions, Middle Ear", "effusion media otitis", "otitis media effusion", "media otitis secretory", "secretory otitis media", "Secretory otitis media", "Secretory Otitis Media", "secretory otitis Media", "otitis; media, effusion", "Otitis Media, Secretory", "Mucoid otitis media NOS", "OTITIS MEDIA, SECRETORY", "Otitis media, secretory", "otitis; media, secretory", "Transudative otitis media", "transudative otitis media", "Otitis media with effusion", "otitis media with effusion", "Otitis media, transudative", "Secretory otitis media NOS", "Otitis Media with Effusion", "media; otitis, transudative", "otitis; media, transudative", "chronic mucoid otitis media", "Otitis media, with effusion", "Chronic middle ear effusion", "Chronic mucoid otitis media", "OTITIS MEDIA, WITH EFFUSION", "Serous otitis media/glue ear", "SOM - Secretory otitis media", "mucoid; otitis media, chronic", "chronic effusion media otitis", "Transudative otitis media NOS", "otitis; media, chronic, mucoid", "Chronic secretory otitis media", "otitis; media, mucoid, chronic", "chronic secretory otitis media", "Serous otitis media (glue ear)", "Chronic otitis media, secretory", "mucoid otitis media (diagnosis)", "OME - Otitis media with effusion", "Chronic mucoid otitis media, NOS", "otitis; media, chronic, effusion", "Chronic transudative otitis media", "otitis; media, chronic, secretory", "chronic transudative otitis media", "otitis; media, secretory, chronic", "Chronic otitis media with effusion", "secretory otitis media (diagnosis)", "Simple chronic mucoid otitis media", "Chronic otitis media, transudative", "mucoid nonsuppurative otitis media", "Otitis media with effusion - mucoid", "Chronic otitis media, with effusion", "transudative; otitis media, chronic", "otitis; media, transudative, chronic", "otitis; media, chronic, transudative", "secretory nonsuppurative otitis media", "transudative otitis media (diagnosis)", "otitis; media, chronic, with effusion", "Chronic mucoid otitis media (disorder)", "Chronic secretory otitis media, mucoid", "Simple chronic mucoid otitis media, NOS", "chronic mucoid otitis media (diagnosis)", "transudative nonsuppurative otitis media", "Chronic MEE - Chronic middle ear effusion", "chronic secretory otitis media (diagnosis)", "Chronic mucoid otitis media, unspecified ear", "secretory chronic nonsuppurative otitis media", "chronic transudative otitis media (diagnosis)", "transudative chronic nonsuppurative otitis media", "Chronic non-suppurative otitis media with effusion", "Chronic mucoid otitis media, simple or unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "otitis media with effusion", "shortest_name_length": 3}
{"curie": "UMLS:C5205910", "names": ["Prostate Malignant Solitary Fibrous Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Malignant Solitary Fibrous Tumor", "shortest_name_length": 41}
{"curie": "MONDO:0013122", "names": ["Glc3d", "GLC3D", "Glaucoma 3, Primary Congenital, D", "glaucoma 3, primary congenital, D", "GLAUCOMA 3, PRIMARY CONGENITAL, D", "glaucoma 3, primary congenital, type D"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glaucoma 3, primary congenital, D", "shortest_name_length": 5}
{"curie": "MONDO:0015439", "names": ["R4", "Ring 4", "syndrome r(4)", "r(4) syndrome", "Syndrome r(4)", "(4)r syndrome", "ROSE Cluster 4", "rose cluster 4", "chromosome 4 ring", "ring chromosome 4", "Ring chromosome 4", "Ring chromosome type 4", "Ring chromosome 4 syndrome", "ring chromosome 4 syndrome", "chromosome 4 ring syndrome", "Ring chromosome 4 syndrome (disorder)", "Ring chromosome 4 syndrome (diagnosis)", "anomaly of chromosome pair ring 4 syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ring chromosome 4", "shortest_name_length": 2}
{"curie": "UMLS:C0004760", "names": ["DYSBARISM", "Dysbarism", "dysbarism", "barotrauma", "Barotrauma", "Barotraumas", "barotraumas", "Barotrauma NOS", "Barotrauma (disorder)", "effects of air pressure", "Effects of air pressure", "effects of; air pressure", "Adverse effect;air pressure", "Effects of air pressure, NOS", "air pressure; adverse effect", "air pressure-related disorder", "Effects of air pressure (disorder)", "effects of air pressure (diagnosis)", "accident caused by changes in air pressure", "accident caused by changes in air pressure (diagnosis)", "Accident due to extremes of atmospheric pressure and to sudden changes in atmospheric pressure", "Accident due to extremes of atmospheric pressure and to sudden changes in atmospheric pressure (event)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Barotrauma", "shortest_name_length": 9}
{"curie": "MONDO:0003092", "names": ["lacrimal gland mucoepidermoid carcinoma", "Lacrimal Gland Mucoepidermoid Carcinoma", "Mucoepidermoid Carcinoma of Lacrimal Gland", "mucoepidermoid carcinoma of lacrimal gland", "mucoepidermoid carcinoma of the lacrimal gland", "Mucoepidermoid Carcinoma of the Lacrimal Gland", "Mucoepidermoid carcinoma of the lacrimal gland", "lacrimal gland malignant carcinoma mucoepidermoid", "mucoepidermoid carcinoma of lacrimal gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lacrimal gland mucoepidermoid carcinoma", "shortest_name_length": 39}
{"curie": "MONDO:0006708", "names": ["Lawsonia infection", "Lawsonia infections", "infection, Lawsonia", "Bilophila infection", "Bilophila infections", "infections, Lawsonia", "infection, Bilophila", "infections, Bilophila", "Desulfovibrio infection", "infection, Desulfovibrio", "Desulfovibrio infections", "infections, Desulfovibrio", "Desulfovibrionaceae Infection", "commensal Bilophila infection", "Desulfovibrionaceae infection", "Infection, Desulfovibrionaceae", "infection, Desulfovibrionaceae", "Desulfovibrionaceae Infections", "Infections, Desulfovibrionaceae", "infections, Desulfovibrionaceae", "Desulfovibrionaceae infectious disease", "Desulfovibrionaceae disease or disorder", "Desulfovibrionaceae caused disease or disorder", "commensal Desulfovibrionaceae infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Desulfovibrionaceae infectious disease", "shortest_name_length": 18}
{"curie": "MONDO:0015198", "names": ["aniridia - ptosis - intellectual disability - familial obesity", "aniridia-ptosis-intellectual disability-familial obesity syndrome", "Aniridia-ptosis-intellectual disability-familial obesity syndrome", "Aniridia, ptosis, intellectual disability, familial obesity syndrome", "Aniridia, ptosis, intellectual disability, familial obesity syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aniridia-ptosis-intellectual disability-familial obesity syndrome", "shortest_name_length": 62}
{"curie": "MONDO:0043257", "names": ["FS", "Wild fire", "wild fire", "fogo selvagem", "Fogo selvagem", "Wildfire pemphigus", "wildfire pemphigus", "amendola's syndrome", "Amendola's syndrome", "Brazilian pemphigus", "Brazilian; pemphigus", "pemphigus; Brazilian", "South American pemphigus", "endemic pemphigus foliaceus", "pemphigus and fogo selvagem", "Endemic pemphigus foliaceus", "Pemphigus and fogo selvagem", "Brazilian pemphigus foliaceus", "Brazilian pemphigus [fogo selvagem]", "Brazilian pemphigus foliaceus (disorder)", "Brazilian pemphigus foliaceus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pemphigus and fogo selvagem", "shortest_name_length": 2}
{"curie": "MONDO:0011022", "names": ["PSS", "P11PDS", "P11pDS", "11p11.2 deletion", "DEFECT11 SYNDROME", "Defect11 syndrome", "Defect11 Syndrome", "POTOCKI-SHAFFER SYNDROME", "Potocki-Shaffer syndrome", "Potocki-Shaffer Syndrome", "proximal 11p deletion syndrome", "PROXIMAL 11p DELETION SYNDROME", "proximal 11P deletion syndrome", "Proximal 11p deletion syndrome", "Proximal 11P deletion syndrome", "deletion of chromosome 11p11.2", "Chromosome 11p11.2 deletion syndrome", "Chromosome 11p11.2 Deletion Syndrome", "CHROMOSOME 11p11.2 DELETION SYNDROME", "chromosome 11P11.2 deletion syndrome", "P11pDS - proximal 11p deletion syndrome", "Chromosome 11p11.2 deletion syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Potocki-Shaffer syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C0154549", "names": ["Musculoskeletal Malfunction Arising from Mental Factor", "Musculoskeletal malfunction arising from mental factors"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Musculoskeletal malfunction arising from mental factors", "shortest_name_length": 54}
{"curie": "UMLS:C2200351", "names": ["Lung Rhabdomyosarcoma", "rhabdomyosarcoma of lung", "Pulmonary Rhabdomyosarcoma", "rhabdomyosarcoma of lung (diagnosis)", "lung neoplasm malignant myosarcoma rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rhabdomyosarcoma of lung", "shortest_name_length": 21}
{"curie": "UMLS:C0275982", "names": ["campylobacteriosis", "Campylobacteriosis", "Diarrhea campylobacter", "Campylobacter diarrhea", "campylobacter diarrhea", "Diarrhoea campylobacter", "Campylobacter enteritis", "Enteritis;campylobacter", "Campylobacter Enteritis", "diarrhea; Campylobacter", "campylobacter enteritis", "CAMPYLOBACTER ENTERITIS", "Campylobacter diarrhoea", "Campylobacter; diarrhea", "Enteric campylobacteriosis", "gastroenteritis campylobacter", "campylobacter gastroenteritis", "Campylobacter Gastroenteritis", "Gastroenteritis campylobacter", "Campylobacter gastroenteritis", "Campylobacter intestinal infection", "gastroenteritis due to Campylobacter", "Enteric campylobacteriosis (disorder)", "Intestinal infection due to campylobacter", "enteritis; infectious, due to Campylobacter", "infectious; enteritis, due to Campylobacter", "Campylobacter gastrointestinal tract infection", "gastroenteritis due to Campylobacter (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Enteric campylobacteriosis", "shortest_name_length": 18}
{"curie": "UMLS:C4527337", "names": ["Refractory Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type", "Refractory Primary Cutaneous (Skin) Diffuse Large B-Cell Lymphoma, Leg Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type", "shortest_name_length": 68}
{"curie": "MONDO:0003713", "names": ["Angiokeratoma circumscriptum", "Angiokeratoma Circumscriptum", "angiokeratoma circumscriptum", "Angiokeratoma circumscriptum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angiokeratoma circumscriptum", "shortest_name_length": 28}
{"curie": "MONDO:0019985", "names": ["drug-related renal tubular dysgenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "drug-related renal tubular dysgenesis", "shortest_name_length": 37}
{"curie": "UMLS:C5555180", "names": ["Refractory Low Grade Fallopian Tube Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Low Grade Fallopian Tube Serous Adenocarcinoma", "shortest_name_length": 57}
{"curie": "MONDO:0012909", "names": ["Skeletal Defects, Genital Hypoplasia, And Mental Retardation", "SKELETAL DEFECTS, GENITAL HYPOPLASIA, AND MENTAL RETARDATION", "skeletal defects, genital hypoplasia, and mental retardation", "skeletal defects, genital hypoplasia, and intellectual disability", "SKELETAL DEFECTS, GENITAL HYPOPLASIA, AND IMPAIRED INTELLECTUAL DEVELOPMENT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skeletal defects, genital hypoplasia, and intellectual disability", "shortest_name_length": 60}
{"curie": "UMLS:C4288008", "names": ["Vulvar Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Germ Cell Tumor", "shortest_name_length": 22}
{"curie": "UMLS:C0280172", "names": ["stage IV grade 3 follicular lymphoma", "Stage IV Grade 3 Follicular Lymphoma", "Grade III Follicular Lymphoma Stage IV", "Stage IV Grade III Follicular Lymphoma", "Stage IV Follicular Large Cell Lymphoma", "Follicular Large Cell Lymphoma Stage IV", "follicular large cell lymphoma, stage IV", "Metastatic Grade III Follicular Lymphoma", "metastatic follicular large cell lymphoma", "follicular large cell lymphoma, metastatic", "Ann Arbor Stage IV Grade 3 Follicular Lymphoma", "stage IV grade III follicular large cell lymphoma", "Stage IV Grade III Follicular Large Cell Lymphoma", "Grade III Stage IV Follicular Large Cell Lymphoma", "Metastatic Grade III Follicular Large Cell Lymphoma", "Grade III Metastatic Follicular Large Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage IV Grade 3 Follicular Lymphoma", "shortest_name_length": 36}
{"curie": "MONDO:0100224", "names": ["MC1DN1", "complex i deficiency", "Complex I deficiency", "Isolated complex I deficiency", "MITOCHONDRIAL COMPLEX I DEFICIENCY", "mitochondrial complex 1 deficiency", "Mitochondrial complex I deficiency", "mitochondrial complex I deficiency", "NADH:Q(1) Oxidoreductase deficiency", "NADH:Q(1) oxidoreductase deficiency", "NADH:Q(1) OXIDOREDUCTASE DEFICIENCY", "NADH coenzyme q reductase deficiency", "NADH-coenzyme Q reductase deficiency", "NADH-COENZYME Q REDUCTASE DEFICIENCY", "Nadh-Coenzyme Q Reductase Deficiency", "Isolated NADH-CoQ reductase deficiency", "Isolated NADH-ubiquinone reductase deficiency", "Isolated NADH-coenzyme Q reductase deficiency", "nuclear type mitochondrial complex I deficiency 1", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1", "mitochondrial complex I deficiency, nuclear type 1", "Isolated mitochondrial respiratory chain complex I deficiency", "Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency", "MITOCHONDRIAL NADH DEHYDROGENASE COMPONENT OF COMPLEX I, DEFICIENCY OF", "mitochondrial NADH dehydrogenase component of Complex I, deficiency of", "Mitochondrial NADH dehydrogenase component of complex I, deficiency of", "NADH - Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency", "Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex I deficiency, nuclear type 1", "shortest_name_length": 6}
{"curie": "MONDO:0010828", "names": ["RP11", "RP 11", "Retinitis Pigmentosa 11", "retinitis pigmentosa 11", "RETINITIS PIGMENTOSA 11", "PRPF31 retinitis pigmentosa", "retinitis pigmentosa type 11", "retinitis pigmentosa caused by mutation in PRPF31"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 11", "shortest_name_length": 4}
{"curie": "UMLS:C0234319", "names": ["Posterior tongue taste disorder", "Glossopharyngeal taste disorder", "Taste Disorder, Posterior Tongue", "Taste disorder, posterior tongue", "Glossopharyngeal taste disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Taste Disorder, Posterior Tongue", "shortest_name_length": 31}
{"curie": "MONDO:0011657", "names": ["DFNA24", "DFNA 24", "autosomal dominant deafness 24", "DEAFNESS, AUTOSOMAL DOMINANT 24", "deafness, autosomal dominant 24", "Deafness, Autosomal Dominant 24", "autosomal dominant nonsyndromic deafness 24", "autosomal dominant nonsyndromic hearing loss 24", "autosomal dominant nonsyndromic deafness type 24", "deafness, autosomal dominant nonsyndromic sensorineural 24"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 24", "shortest_name_length": 6}
{"curie": "MONDO:0019229", "names": ["disorder of ketolysis", "inborn disorder of ketolysis", "inborn ketone body catabolic process disorder", "inborn error of ketone body catabolic process", "rare inborn error of ketone body catabolic process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of ketolysis", "shortest_name_length": 21}
{"curie": "UMLS:C0855144", "names": ["Stage III Nodal Marginal Zone Lymphoma", "Nodal Marginal Zone B-Cell Lymphoma Stage III", "Nodal marginal zone B-cell lymphoma stage III", "Stage III Nodal Marginal Zone B-Cell Lymphoma", "Ann Arbor Stage III Nodal Marginal Zone Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nodal marginal zone B-cell lymphoma stage III", "shortest_name_length": 38}
{"curie": "UMLS:C5238872", "names": ["Sternotomy Scar", "Sternotomy scar"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sternotomy Scar", "shortest_name_length": 15}
{"curie": "MONDO:0000693", "names": ["bipolar 2 disorder", "Bipolar 2 disorder", "bipolar disorder ii", "bipolar ii disorder", "bipolar ll disorder", "bipolar II disorder", "Bipolar II disorder", "bipolar; disorder, II", "disorder; bipolar, II", "Bipolar Disorder Type 2", "Type 2 Bipolar Disorder", "Bipolar II disorder, NOS", "Bipolar disorder, Type 2", "Bipolar disorder, type 2", "Bipolar II disorder (disorder)", "bipolar II disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bipolar II disorder", "shortest_name_length": 18}
{"curie": "MONDO:0004320", "names": ["adult infiltrating astrocytoma", "adult Infiltrating astrocytoma", "Adult Infiltrating Astrocytoma", "astrocytoma, adult infiltrating", "adult Infiltrating Astrocytic tumor", "adult infiltrating astrocytic tumor", "Adult Infiltrating Astrocytic Tumor", "Adult Infiltrating Astrocytic Neoplasm", "adult infiltrating astrocytic neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult infiltrating astrocytic neoplasm", "shortest_name_length": 30}
{"curie": "UMLS:C1882989", "names": ["Secondary caries", "Secondary Caries", "Secondary caries (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary caries", "shortest_name_length": 16}
{"curie": "MONDO:0009835", "names": ["sspe", "SSPE", "Dawson", "Van Bogaert", "Dawson disease", "Bodechtel-Guttman", "Dawson encephalitis", "Van Bogaert disease", "encephalitis; Dawson", "Dawson; encephalitis", "Dawson's encephalitis", "DEMENTIA, DECEREBRATE", "Van Bogaert encephalitis", "leukencephalitis; Van Bogaert", "Van Bogaert Leukoencephalitis", "Van Bogaert; leukencephalitis", "Leukoencephalitis, Van Bogaert", "Van Bogaert; leukoencephalitis", "Van Bogaerts Leukoencephalitis", "leukoencephalitis; Van Bogaert", "Leukoencephalitis, Van Bogaerts", "Van Bogaert's Leukoencephalitis", "Leukoencephalitis, Van Bogaert's", "SUBACUTE SCLEROSING PANENCEPHALITIS", "Measles Inclusion Body Encephalitis", "Subacute Sclerosing Panencephalitis", "Measles inclusion body encephalitis", "subacute sclerosing panencephalitis", "Subacute sclerosing panencephalitis", "Sclerosing Panencephalitis, Subacute", "Panencephalitis, Subacute Sclerosing", "panencephalitis, SUBACUTE sclerosing", "Subacute inclusion body encephalitis", "subacute inclusion body encephalitis", "Inclusion Body Encephalitis, Measles", "Dawson's inclusion body encephalitis", "PANENCEPHALITIS, SUBACUTE SCLEROSING", "panencephalitis; subacute sclerosing", "leukencephalitis; subacute sclerosing", "Subacute sclerosing leukoencephalitis", "Encephalitis, Inclusion Body, Measles", "Subacute Sclerosing Panencephalitides", "Subacute Sclerosing Leukoencephalitis", "subacute sclerosing; leukencephalitis", "Panencephalitides, Subacute Sclerosing", "leukoencephalitis; subacute sclerosing", "Sclerosing Leukoencephalitis, Subacute", "Sclerosing Panencephalitides, Subacute", "subacute sclerosing; leukoencephalitis", "Leukoencephalitis, Subacute Sclerosing", "Immunosuppressive measles encephalitis", "subacute sclerosing leukoencephalopathy", "Subacute Sclerosing Leukoencephalitides", "Van Bogaert sclerosing leukoencephalitis", "Van Bogaert sclerosing leucoencephalitis", "Leukoencephalitides, Subacute Sclerosing", "Sclerosing Leukoencephalitides, Subacute", "subacute sclerosing panencephalitis (SSPE)", "SSPE - Subacute sclerosing panencephalitis", "SSPE (subacute sclerosing panencephalitis)", "Van Bogaert's sclerosing leukoencephalitis", "Subacute sclerosing panencephalitis (SSPE)", "Van Bogaert's sclerosing leucoencephalitis", "van Bogaert's sclerosing leukoencephalitis", "MIBE - Measles inclusion body encephalitis", "Measles inclusion body encephalitis (disorder)", "Subacute sclerosing panencephalitis (disorder)", "subacute sclerosing panencephalitis (diagnosis)", "Van Bogaert's sclerosing leukoencephalitis (disorder)", "Van Bogaert's sclerosing leukoencephalitis (diagnosis)", "Subacute sclerosing panencephalitis (disorder) [ambiguous]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subacute sclerosing panencephalitis", "shortest_name_length": 4}
{"curie": "UMLS:C1519787", "names": ["Undifferentiated", "Undifferentiated Neuroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Undifferentiated Neuroblastoma", "shortest_name_length": 16}
{"curie": "MONDO:0008390", "names": ["Rombo syndrome", "ROMBO SYNDROME", "Rombo syndrome (disorder)", "vermiculate atrophoderma, milia, hypotrichosis, trichoepitheliomas, basal cell carcinomas and peripheral vasodilation with cyanosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rombo syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C1955629", "names": ["Human herpesvirus 6 encephalitis", "Human Herpesvirus 6 encephalitis", "encephalitis due to human herpesvirus 6", "Encephalitis due to human herpesvirus 6 infection", "encephalitis due to human herpesvirus 6 (diagnosis)", "Encephalitis caused by human herpesvirus 6 infection", "Encephalitis caused by human herpesvirus 6 infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Human Herpesvirus 6 encephalitis", "shortest_name_length": 32}
{"curie": "MONDO:0013142", "names": ["HSAN2B", "Hereditary sensory autonomic neuropathy type IIB", "hereditary sensory and autonomic neuropathy type 2B", "hereditary sensory and autonomic neuropathy type IIB", "neuropathy, hereditary sensory and autonomic, type 2B", "Neuropathy, Hereditary Sensory And Autonomic, Type IIB", "neuropathy, hereditary sensory and autonomic, type IIB", "NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIB", "RETREG1 hereditary sensory and autonomic neuropathy type 2", "Hereditary sensory autonomic neuropathy type IIB (disorder)", "hereditary sensory and autonomic neuropathy type 2 caused by mutation in RETREG1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuropathy, hereditary sensory and autonomic, type 2B", "shortest_name_length": 6}
{"curie": "MONDO:0011476", "names": ["BLSI", "BLS type 1", "BLS, TYPE I", "Bls, type 1", "BLS, Type I", "BLS, type I", "HLA Class 1 deficiency", "HLA CLASS I deficiency", "HLA CLASS I DEFICIENCY", "HLA Class I Deficiency", "MHC class I deficiency", "Bare Lymphocyte Syndrome Type 1", "Bare lymphocyte syndrome type I", "Bare lymphocyte syndrome type 1", "bare lymphocyte syndrome type I", "Bare Lymphocyte Syndrome, Type I", "BARE LYMPHOCYTE SYNDROME, TYPE I", "BARE lymphocyte syndrome, type I", "Bare lymphocyte syndrome, type 1", "bare lymphocyte syndrome type I (diagnosis)", "Immunodeficiency by defective expression of MHC class I", "immunodeficiency by defective expression of HLA class 1", "Immunodeficiency by Defective Expression of MHC Class I", "bare lymphocyte syndrome, type I, due to TAP2 deficiency", "immunodeficiency by defective expression of HLA class type 1", "Immunodeficiency by defective expression of human leukocyte antigen class 1", "Immunodeficiency by defective expression of human leukocyte antigen class I", "immunodeficiency by defective expression of human leukocyte antigen class 1", "Immunodeficiency by defective expression of HLA (human leukocyte antigen) class 1", "Immunodeficiency by defective expression of human leukocyte antigen class 1 (disorder)", "immunodeficiency by defective expression of human leukocyte antigen class 1 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MHC class I deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0001971", "names": ["FARMER LUNG", "Farmer Lung", "farmer lung", "Farmers lung", "farmers lung", "Farmers Lung", "farmers' lung", "farmers lungs", "Farmers' lung", "Farmer's Lung", "farmer's lung", "Farmer's lung", "farmer's lungs", "Farmer's Lungs", "thresher's lung", "Thresher's lung", "Moldy hay disease", "Moldy-hay disease", "Mouldy-hay disease", "Mouldy hay disease", "moldy hay; disease", "farmer's lung disease", "Farmer's lung disease", "Farmers' lung disease", "diseases farmer's lung", "Farmers' lung (disorder)", "moldy hay; pneumoconiosis", "pneumoconiosis; moldy hay", "farmers' lung (diagnosis)", "disease (or disorder); moldy hay", "lung; fibrosis, with farmer's lung", "fibrosis; lung, with farmer's lung", "pneumonitis; hypersensitivity, haymaker's", "hypersensitivity; pneumonitis, haymaker's", "pneumonitis; hypersensitivity, harvester's", "hypersensitivity; pneumonitis, harvester's"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "farmer's lung disease", "shortest_name_length": 11}
{"curie": "MONDO:0005647", "names": ["Condyloma", "condyloma", "Genital wart", "Genital Wart", "GENITAL WART", "genital wart", "Venereal wart", "genital Warts", "Wart, Genital", "Venereal Wart", "venereal wart", "genital warts", "Genital warts", "Genital Warts", "Warts, Genital", "venereal; wart", "venereal warts", "Venereal warts", "wart; venereal", "genitals warts", "Wart, Venereal", "Venereal Warts", "Anogenital wart", "Warts, Venereal", "anogenital wart", "wart anogenital", "wart; anogenital", "Anogenital warts", "warts anogenital", "anogenital warts", "anogenital; wart", "anogenital Warts", "verruca acuminata", "venereal; verruca", "Verruca acuminata", "Genital warts NOS", "verruca; venereal", "acuminata; verruca", "verruca; acuminata", "CONDYLOMA ACUMINATA", "Condyloma Acuminata", "condyloma acuminata", "CONDYLOMA ACUMINATUM", "acuminata condylomas", "condyloma acuminatum", "Condyloma Accuminata", "Condyloma acuminatum", "Condyloma Acuminatum", "acuminata; condyloma", "condyloma accuminata", "CONDYLOMA ACCUMINATA", "condyloma; acuminata", "condylomata acuminata", "Condylomata Acuminata", "Condylomata acuminata", "Condylomata acuminate", "acuminata condylomata", "Condylomata acuminatum", "AGW - Anogenital warts", "condylomata acuminatum", "anogenital venereal wart", "Genital warts (disorder)", "genital warts (diagnosis)", "Anogenital (venereal) warts", "Anogenital warts (disorder)", "Genital wart virus infection", "anogenital warts (diagnosis)", "WVI - Genital wart virus infection", "genital wart virus infectious disease", "Anogenital Human Papillomavirus Infection", "anogenital Human Papillomavirus infection", "anogenital human papillomavirus infection", "Anogenital human papillomavirus infection", "anogenital Human papilloma Virus infection", "Anogenital Human Papilloma Virus Infection", "Anogenital human papilloma virus infection", "human papilloma virus infection anogenital", "Condyloma acuminatum of the anogenital region", "Condylomata acuminatum of the anogenital region", "HPV - Anogenital human papilloma virus infection", "anogenital Human papilloma Virus infectious disease", "Anogenital Human papilloma Virus Infectious Disease", "Anogenital human papillomavirus infection (disorder)", "Anogenital human papillomavirus infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anogenital human papillomavirus infection", "shortest_name_length": 9}
{"curie": "MONDO:0003439", "names": ["bladder villous adenoma", "Bladder Villous Adenoma", "urinary bladder villous adenoma", "Urinary Bladder Villous Adenoma", "Villous Adenoma of Urinary Bladder", "villous adenoma of urinary bladder", "Villous Adenoma of the Urinary Bladder", "villous adenoma of the urinary bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urinary bladder villous adenoma", "shortest_name_length": 23}
{"curie": "UMLS:C2242496", "names": ["Parotid gland inflammation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parotid gland inflammation", "shortest_name_length": 26}
{"curie": "MONDO:0019093", "names": ["Functional antibody defect", "Specific antibody deficiency", "specific antibody deficiency", "Abnormal specific antibody response", "Decreased specific antibody in blood", "Specific immunoglobulin response defect", "Specific antibody deficiency (disorder)", "specific antibody deficiency (diagnosis)", "Decreased circulating level of specific antibody", "immunodeficiency due to selective anti-polysaccharide antibody deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency due to selective anti-polysaccharide antibody deficiency", "shortest_name_length": 26}
{"curie": "MONDO:0007029", "names": ["bor syndrome", "BOR Syndrome", "BOR syndrome", "MELNICK-FRASER SYNDROME", "Melnick Fraser Syndrome", "Melnick-Fraser Syndrome", "Melnick-Fraser syndrome", "branchiootorenal syndrome", "Branchiootorenal syndrome", "BRANCHIOOTORENAL DYSPLASIA", "Branchiootorenal Dysplasia", "branchio otorenal syndrome", "Branchiootorenal dysplasia", "branchio-otorenal syndrome", "Branchio-Otorenal Syndrome", "branchiootorenal dysplasia", "Dysplasia, Branchiootorenal", "Branchio-otorenal dysplasia", "Branchio oto renal syndrome", "Branchio-oto-renal Syndrome", "branchio-oto-renal syndrome", "Branchio-oto-renal syndrome", "Branchio-Oto-Renal Syndrome", "branchio oto renal syndrome", "Branchio-Otorenal Dysplasia", "Branchio Oto Renal Syndrome", "Branchio-Oto-renal syndrome", "Melnick-Fraser syndrome (disorder)", "branchio-oto-renal syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "branchio-oto-renal syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0006557", "names": ["Subcutaneous Angioma", "subcutaneous angioma", "subcutaneous hemangioma", "Subcutaneous hemangioma", "Subcutaneous Hemangioma", "Subcutaneous haemangioma", "subcutaneous haemangioma", "Subcutaneous Tissue Angioma", "subcutaneous tissue angioma", "superficial fascia hemangioma", "hemangioma subcutaneous tissue", "angioma of subcutaneous tissue", "Angioma of Subcutaneous Tissue", "Subcutaneous Tissue Hemangioma", "subcutaneous tissue hemangioma", "hemangioma of superficial fascia", "Hemangioma of subcutaneous tissue", "hemangioma of subcutaneous tissue", "Hemangioma of Subcutaneous Tissue", "angioma of the subcutaneous tissue", "Haemangioma of subcutaneous tissue", "Angioma of the Subcutaneous tissue", "Angioma of the Subcutaneous Tissue", "Hemangioma of the Subcutaneous Tissue", "hemangioma of the subcutaneous tissue", "hemangioma subcutaneous tissue (diagnosis)", "Hemangioma of subcutaneous tissue (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemangioma of subcutaneous tissue", "shortest_name_length": 20}
{"curie": "MONDO:0700157", "names": ["canine oral squamous cell carcinoma", "Canine Oral Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canine oral squamous cell carcinoma", "shortest_name_length": 35}
{"curie": "MONDO:0014454", "names": ["HKLLS2", "FAT4 Hennekam syndrome", "Hennekam syndrome caused by mutation in FAT4", "Hennekam lymphangiectasia-lymphedema syndrome 2", "HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2", "Hennekam lymphangiectasia-lymphedema syndrome type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hennekam lymphangiectasia-lymphedema syndrome 2", "shortest_name_length": 6}
{"curie": "MONDO:0024950", "names": ["disease horse", "horse disease", "Horse Disease", "horse diseases", "disease, horse", "Horse Diseases", "Equine Disease", "disease horses", "Disease, Horse", "equine disease", "Diseases, Horse", "Equine Diseases", "diseases, horse", "equine diseases", "Disease, Equine", "disease, equine", "diseases horses", "diseases, equine", "Horses--Diseases", "Diseases, Equine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "horse disease", "shortest_name_length": 13}
{"curie": "UMLS:C1868855", "names": ["Post procedural infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post procedural infection", "shortest_name_length": 25}
{"curie": "MONDO:0011384", "names": ["Hyt1", "HYT1", "hypertension, essential, susceptibility to, 1", "HYPERTENSION, ESSENTIAL, SUSCEPTIBILITY TO, 1", "hypertension, essential, susceptibility to, type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertension, essential, susceptibility to, 1", "shortest_name_length": 4}
{"curie": "MONDO:0007477", "names": ["3M1", "3-MSBN", "3M Syndrome", "3M SYNDROME", "3M syndrome", "3-M syndrome", "3-M Syndrome", "Three M Syndrome", "three M syndrome", "Le Merrer syndrome", "three M syndrome 1", "gloomy face syndrome", "Dolichospondylic dysplasia", "dolichospondylic dysplasia", "dwarfism with tall vertebrae", "three-M slender-boned nanism", "Yakut short stature syndrome", "Miller-McKusick-Malvaux-Syndrome", "Miller-McKusick-Malvaux syndrome", "Dolichospondylic dysplasia (disorder)", "Miller-McKusick-Malvaux-Syndrome (3M Syndrome)", "gloomy face syndrome Yakut short stature syndrome, included"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "3-M syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C4744535", "names": ["Hobnail Variant Thyroid Gland Papillary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hobnail Variant Thyroid Gland Papillary Carcinoma", "shortest_name_length": 49}
{"curie": "MONDO:0009145", "names": ["SSPS", "Schopf-Schulz-Passarge syndrome", "SChöPF-Schulz-Passarge syndrome", "Schöpf-Schulz-Passarge syndrome", "SCHOPF-Schulz-Passarge syndrome", "Schopf-Schulz-Passarge Syndrome", "SCHOPF-SCHULZ-PASSARGE SYNDROME", "SchC6pf-Schulz-Passarge syndrome", "eccrine tumors-ectodermal dysplasia", "Eccrine tumors-ectodermal dysplasia", "Eccrine Tumors With Ectodermal Dysplasia", "eccrine tumors with ectodermal dysplasia", "ECCRINE TUMORS WITH ECTODERMAL DYSPLASIA", "SCHOPF-SCHULZ-PASSARGE SYNDROME (disorder)", "Schöpf-Schulz-Passarge syndrome (disorder)", "keratosis palmoplantaris-cystic eyelids-hypodontia-hypotrichosis syndrome", "palmoplantar keratoderma-cystic eyelids-hypodontia-hypotrichosis syndrome", "Palmoplantar keratoderma-cystic eyelids-hypodontia-hypotrichosis syndrome", "Keratosis palmoplantaris-cystic eyelids-hypodontia-hypotrichosis syndrome", "KERATOSIS PALMOPLANTARIS WITH CYSTIC EYELIDS, HYPODONTIA, AND HYPOTRICHOSIS", "keratosis palmoplantaris with cystic eyelids, hypodontia, and hypotrichosis", "Keratosis Palmoplantaris With Cystic Eyelids, Hypodontia, And Hypotrichosis", "Palmoplantar hyperkeratosis-cystic eyelids-hypodontia-hypotrichosis syndrome", "palmoplantar hyperkeratosis-cystic eyelids-hypodontia-hypotrichosis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SchC6pf-Schulz-Passarge syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C1511086", "names": ["Benign Cervical Mixed Epithelial and Mesenchymal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Cervical Mixed Epithelial and Mesenchymal Neoplasm", "shortest_name_length": 57}
{"curie": "UMLS:C0027645", "names": ["neoplasm seeding", "Neoplasm Seeding", "Seeding, Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplasm Seeding", "shortest_name_length": 16}
{"curie": "UMLS:C0280176", "names": ["high-grade, stage IV adult NHL", "NHL, high grade, stage IV adult", "adult NHL, stage IV, high grade", "high-grade, metastatic adult NHL", "adult NHL, metastatic, high grade", "NHL, high grade, metastatic adult", "Stage IV High Grade Adult Non-Hodgkin's Lymphoma", "adult non-Hodgkin's lymphoma, high grade, stage IV", "lymphoma, high grade, stage IV adult non-Hodgkin's", "non-Hodgkin's lymphoma, high grade, stage IV adult", "high-grade, metastatic adult non-Hodgkin's lymphoma", "lymphoma, high grade, metastatic adult non-Hodgkin's", "non-Hodgkin's lymphoma, high grade, metastatic adult", "adult non-Hodgkin's lymphoma, high grade, metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV High Grade Adult Non-Hodgkin's Lymphoma", "shortest_name_length": 30}
{"curie": "UMLS:C0239707", "names": ["Digestive Angioma", "Digestive Hemangioma", "Gastrointestinal Angioma", "Digestive System Angioma", "Digestive System Hemangioma", "GASTROINTESTINAL HEMANGIOMA", "Gastrointestinal Hemangioma", "Angioma of Digestive System", "Hemangioma of Digestive System", "Angioma of the Digestive System", "Gastrointestinal System Angioma", "Gastrointestinal System Hemangioma", "Angioma of Gastrointestinal System", "Hemangioma of the Digestive System", "Hemangioma of Gastrointestinal System", "Angioma of the Gastrointestinal System", "Hemangioma of the Gastrointestinal System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Digestive System Hemangioma", "shortest_name_length": 17}
{"curie": "MONDO:0000894", "names": ["mucinous bronchioloalveolar adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucinous bronchioloalveolar adenocarcinoma", "shortest_name_length": 42}
{"curie": "UMLS:C0161803", "names": ["pancreas transplant; complications", "Transplanted Pancreas Complication", "complications; pancreas transplant", "complications of pancreas transplant", "Complication of transplanted pancreas", "Complications of transplanted pancreas", "complications of pancreas transplant (diagnosis)", "Complication of transplanted pancreas (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Complication of transplanted pancreas", "shortest_name_length": 34}
{"curie": "MONDO:0005310", "names": ["FLUTTER ATRIAL", "Flutter atrial", "Flutter;atrial", "Atrial flutter", "atrial flutter", "Atrial Flutter", "ATRIAL FLUTTER", "atrium; flutter", "Flutter, Atrial", "Atrial Flutters", "Flutters, Atrial", "flutter auricular", "Auricular Flutter", "auricular; flutter", "Flutter, Auricular", "Auricular Flutters", "Flutters, Auricular", "atrial flutter (disease)", "Atrial flutter (disorder)", "atrial flutter (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial flutter", "shortest_name_length": 14}
{"curie": "UMLS:C1333433", "names": ["EBV-Related Non-Hodgkin Lymphoma", "EBV Related Non-Hodgkin's Lymphoma", "EBV-Related Non-Hodgkin's Lymphoma", "Epstein-Barr Virus-Related Non-Hodgkin Lymphoma", "Epstein-Barr Virus-Related Non-Hodgkin's Lymphoma", "Epstein-Barr Virus Related Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "EBV-Related Non-Hodgkin Lymphoma", "shortest_name_length": 32}
{"curie": "MONDO:0056797", "names": ["NEDMHM", "NEURODEVELOPMENTAL DISORDER WITH MIDBRAIN AND HINDBRAIN MALFORMATIONS", "neurodevelopmental disorder with midbrain and hindbrain malformations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with midbrain and hindbrain malformations", "shortest_name_length": 6}
{"curie": "MONDO:0008465", "names": ["Patterson-Stevenson syndrome", "Patterson-Stevenson-Fontaine syndrome", "PATTERSON-STEVENSON-FONTAINE SYNDROME", "Patterson Stevenson Fontaine syndrome", "Patterson Stevenson Fontaine syndrome (disorder)", "Patterson Stevenson Fontaine syndrome (diagnosis)", "split-foot deformity with mandibulofacial dysostosis", "SPLIT-FOOT DEFORMITY WITH MANDIBULOFACIAL DYSOSTOSIS", "split foot deformity-mandibulofacial dysostosis syndrome", "Split foot deformity-mandibulofacial dysostosis syndrome", "Split foot deformity with mandibulofacial dysostosis syndrome", "split-foot deformity with ectrodactyly and mandibulofacial dysostosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Patterson-Stevenson-Fontaine syndrome", "shortest_name_length": 28}
{"curie": "UMLS:C5418301", "names": ["Recurrent Acute Promyelocytic Leukemia with PML-RARA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Acute Promyelocytic Leukemia with PML-RARA", "shortest_name_length": 52}
{"curie": "UMLS:C0403632", "names": ["Cystitis noninfective", "cystitis non-infective", "Non-infective cystitis", "Non-Infectious Cystitis", "Non-infective cystitis (disorder)", "Non-infective cystitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Infectious Cystitis", "shortest_name_length": 21}
{"curie": "MONDO:0019575", "names": ["hypotrichosis simplex of the scalp", "hereditary hypotrichosis simplex of the scalp"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotrichosis simplex of the scalp", "shortest_name_length": 34}
{"curie": "MONDO:0004667", "names": ["sublingual gland cancer", "cancer of sublingual gland", "malignant sublingual gland tumor", "Malignant Sublingual Gland Tumor", "Malignant tumor of sublingual gland", "Malignant Sublingual Gland Neoplasm", "malignant sublingual gland neoplasm", "malignant tumor of sublingual gland", "Malignant Tumor of Sublingual Gland", "Malignant tumour of sublingual gland", "Malignant Neoplasm of Sublingual Gland", "Malignant neoplasm of sublingual gland", "malignant neoplasm of sublingual gland", "malignant tumor of the Sublingual gland", "malignant tumor of the sublingual gland", "Malignant Tumor of the Sublingual Gland", "Malignant Neoplasm of the Sublingual Gland", "malignant neoplasm of the sublingual gland", "Malignant tumor of sublingual gland (disorder)", "malignant neoplasm of sublingual gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sublingual gland cancer", "shortest_name_length": 23}
{"curie": "MONDO:0015768", "names": ["5p trisomy", "trisomy 5p", "Duplication 5p", "5p duplication", "trisomy type 5p", "partial trisomy 5p", "chromosome 5p duplication", "trisomy of the short arm of chromosome 5", "Duplication of the short arm of chromosome 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trisomy 5p", "shortest_name_length": 10}
{"curie": "UMLS:C5667177", "names": ["Recurrent HIV-Related Lymphoproliferative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent HIV-Related Lymphoproliferative Disorder", "shortest_name_length": 50}
{"curie": "UMLS:C0392536", "names": ["Induced abortion failed", "Abortion, failed attempt", "failed attempted abortion", "Failed attempted abortion", "induction; abortion, failure", "failure; induction of abortion", "Failed attempted abortion (disorder)", "failed attempted abortion (diagnosis)", "Failed attempted termination of pregnancy", "TOP - Failed attempted termination of pregnancy", "failure of attempted induction of termination of pregnancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Failed attempted abortion", "shortest_name_length": 23}
{"curie": "MONDO:0016020", "names": ["Frontal Encephalocele", "frontal encephalocele", "Frontal encephalocele", "encephalocele frontal", "Encephalocele, Frontal", "anterior encephalocele", "encephalocele; frontal", "frontal; encephalocele", "Frontal Encephaloceles", "Anterior encephalocele", "Encephaloceles, Frontal", "Frontal encephalocele (disorder)", "frontal encephalocele (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontal encephalocele", "shortest_name_length": 21}
{"curie": "UMLS:C1699588", "names": ["larynx; fistula", "fistula; larynx", "laryngeal fistula", "Laryngeal Fistula", "Laryngeal fistula", "laryngeal fistula (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laryngeal Fistula", "shortest_name_length": 15}
{"curie": "UMLS:C0677684", "names": ["Stage I Aggressive Non-Hodgkin Lymphoma", "stage I aggressive adult non-Hodgkin lymphoma", "Stage I Aggressive Adult Non-Hodgkin Lymphoma", "aggressive, stage I adult non-Hodgkin lymphoma", "stage I aggressive adult non-Hodgkin's lymphoma", "aggressive stage I adult non-Hodgkin's lymphoma", "Stage I Aggressive Adult Non-Hodgkin's Lymphoma", "Aggressive Stage I Adult Non-Hodgkin's Lymphoma", "aggressive adult non-Hodgkin's lymphoma stage I", "Aggressive Adult Non-Hodgkin's Lymphoma Stage I", "Ann Arbor Stage I Aggressive Adult Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage I Aggressive Adult Non-Hodgkin Lymphoma", "shortest_name_length": 39}
{"curie": "UMLS:C0751958", "names": ["Lymphoma, Lymphocytic, Intermediate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoma, Lymphocytic, Intermediate", "shortest_name_length": 35}
{"curie": "MONDO:0010839", "names": ["HMN8", "DHMN8", "neuropathy, distal hereditary motor, type 8", "distal hereditary motor neuronopathy type 8", "distal hereditary motor neuropathy type VIII", "neuronopathy, distal hereditary motor, type 8", "NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VIII", "NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIII", "neuronopathy, distal hereditary motor, type VIII", "congenital nonprogressive spinal muscular atrophy", "Congenital nonprogressive spinal muscular atrophy", "autosomal dominant benign distal spinal muscular atrophy", "Autosomal dominant benign distal spinal muscular atrophy", "spinal muscular atrophy, distal, congenital nonprogressive", "Congenital benign spinal muscular atrophy with contracture", "Spinal Muscular Atrophy, Distal, Congenital Nonprogressive", "SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE", "Congenital benign spinal muscular atrophy with contractures", "congenital benign spinal muscular atrophy with contractures", "autosomal dominant congenital benign spinal muscular atrophy", "Autosomal dominant congenital benign spinal muscular atrophy", "Spinal Muscular Atrophy, Congenital Benign, with Contractures", "SPINAL MUSCULAR ATROPHY, CONGENITAL BENIGN, WITH CONTRACTURES", "spinal muscular atrophy, congenital benign, with contractures", "Autosomal dominant congenital benign spinal muscular atrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant congenital benign spinal muscular atrophy", "shortest_name_length": 4}
{"curie": "UMLS:C4725817", "names": ["Refractory Malignant Endocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Malignant Endocrine Neoplasm", "shortest_name_length": 39}
{"curie": "UMLS:C0919980", "names": ["VIIth nerve palsy", "VIIth nerve paralysis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "VIIth nerve palsy", "shortest_name_length": 17}
{"curie": "MONDO:0011306", "names": ["MUSCULAR DYSTROPHY, CONGENITAL, WITH CEREBELLAR ATROPHY", "Muscular Dystrophy, Congenital, With Cerebellar Atrophy", "muscular dystrophy, congenital, with cerebellar atrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy, congenital, with cerebellar atrophy", "shortest_name_length": 55}
{"curie": "MONDO:0024626", "names": ["Defective phagocytic cell killing", "defective phagocytic cell killing", "defective phagocytic cell engulfment", "Defective phagocytic cell killing (disorder)", "defective phagocytic cell killing (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "defective phagocytic cell engulfment", "shortest_name_length": 33}
{"curie": "UMLS:C2930987", "names": ["Sinonasal Teratocarcinosarcoma", "Sinonasal teratocarcinosarcoma", "Paranasal sinus teratocarcinosarcoma", "Sinonasal teratocarcinosarcoma (type)", "Paranasal sinus teratocarcinosarcoma (type)", "Nasal Cavity and Paranasal Sinus Teratocarcinosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paranasal sinus teratocarcinosarcoma (type)", "shortest_name_length": 30}
{"curie": "MONDO:0100151", "names": ["CTNS", "Nephropathic Cystinoses", "Nephropathic Cystinosis", "nephropathic cystinosis", "Nephropathic cystinosis", "Cystinoses, Nephropathic", "CYSTINOSIS, NEPHROPATHIC", "cystinosis, nephropathic", "Cystinosis, Nephropathic", "cystinosis infantile nephropathic", "cystinosis, atypical nephropathic", "Infantile nephropathic cystinosis", "infantile nephropathic cystinosis", "CYSTINOSIS, ATYPICAL NEPHROPATHIC", "Cystinosis, Infantile Nephropathic", "CYSTINOSIS, INFANTILE NEPHROPATHIC", "Abderhalden Lignac Kaufmann disease", "Abderhalden-Lignac-Kaufmann disease", "Abderhalden Kaufmann Lignac syndrome", "Abderhalden-Kaufmann-Lignac syndrome", "Infantile nephropathic cystinosis (disorder)", "CYSTINOSIS, ATYPICAL NEPHROPATHIC (disorder)", "infantile nephropathic cystinosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephropathic cystinosis", "shortest_name_length": 4}
{"curie": "MONDO:0014715", "names": ["IMD44", "IMMUNODEFICIENCY 44", "immunodeficiency 44", "immunodeficiency type 44", "primary immunodeficiency with post-MMR vaccine viral infection", "primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection", "shortest_name_length": 5}
{"curie": "MONDO:0013537", "names": ["DFNB29", "autosomal recessive deafness 29", "deafness, autosomal recessive 29", "DEAFNESS, AUTOSOMAL RECESSIVE 29", "deafness, autosomal recessive type 29", "autosomal recessive nonsyndromic deafness 29", "CLDN14 autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 29", "autosomal recessive nonsyndromic deafness type 29", "autosomal recessive nonsyndromic deafness caused by mutation in CLDN14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 29", "shortest_name_length": 6}
{"curie": "UMLS:C4289690", "names": ["Diffuse Glioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse Glioma", "shortest_name_length": 14}
{"curie": "UMLS:C1336257", "names": ["stage 3 neuroblastoma", "Stage 3 Neuroblastoma", "Stage III Neuroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 3 Neuroblastoma", "shortest_name_length": 21}
{"curie": "UMLS:C4744699", "names": ["Intrathyroidal Thymoma", "Ectopic Thyroid Gland Thymoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intrathyroidal Thymoma", "shortest_name_length": 22}
{"curie": "MONDO:0008809", "names": ["polyneuropathy, hand defect", "Hamanishi-Ueba-Tsuji syndrome", "Hamanishi Ueba Tsuji syndrome", "polyneuropathy-hand defect syndrome", "Polyneuropathy-hand defect syndrome", "Polyneuropathy, hand defect syndrome", "digital extensor muscle aplasia-polyneuropathy", "Digital extensor muscle aplasia-polyneuropathy", "Digital extensor muscle aplasia with polyneuropathy", "Digital extensor muscle aplasia with polyneuropathy (disorder)", "APLASIA OF EXTENSOR MUSCLES OF FINGERS, UNILATERAL, WITH GENERALIZED POLYNEUROPATHY", "aplasia of extensor muscles of fingers, unilateral, with generalized polyneuropathy", "Aplasia of Extensor Muscles of Fingers, Unilateral, with Generalized Polyneuropathy", "Congenital aplasia of extensor muscle of finger and thumb associated with generalised polyneuropathy", "Congenital aplasia of extensor muscle of finger and thumb associated with generalized polyneuropathy", "congenital aplasia of the extensor muscles of the fingers and thumb associated with generalized polyneuropathy", "Congenital aplasia of the extensor muscles of the fingers and thumb associated with generalized polyneuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyneuropathy-hand defect syndrome", "shortest_name_length": 27}
{"curie": "UMLS:C4683661", "names": ["Follicular Lymphoma by Ann Arbor Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Follicular Lymphoma by Ann Arbor Stage", "shortest_name_length": 38}
{"curie": "MONDO:0007491", "names": ["Dystelephalangy", "dystelephalangy", "DYSTELEPHALANGY", "Kirner deformity", "KIRNER DEFORMITY", "congenital bilateral metadiaphyseal acrodysplasia of the little finger"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dystelephalangy", "shortest_name_length": 15}
{"curie": "MONDO:0011764", "names": ["PARK8", "Parkinson disease 8", "Parkinson's disease 8", "LRRK2 Parkinson disease", "PARKINSON DISEASE 8 (disorder)", "autosomal dominant Parkinson disease 8", "Parkinson disease 8, autosomal dominant", "PARKINSON DISEASE 8, AUTOSOMAL DOMINANT", "autosomal dominant Parkinson's disease 8", "autosomal dominant Parkinson disease type 8", "Parkinson disease caused by mutation in LRRK2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant Parkinson disease 8", "shortest_name_length": 5}
{"curie": "UMLS:C1535916", "names": ["Pelvic Floor Muscle Weakness", "pelvic floor muscle weakness", "Pelvic floor muscle weakness", "pelvic floor muscle weakness (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pelvic Floor Muscle Weakness", "shortest_name_length": 28}
{"curie": "UMLS:C4553419", "names": ["III", "Stage III Cervical Cancer", "Stage III Cervical Cancer AJCC v8", "Stage III Cervical Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Cervical Cancer AJCC v8", "shortest_name_length": 3}
{"curie": "MONDO:0007651", "names": ["gastrocutaneous syndrome", "Gastrocutaneous syndrome", "GASTROCUTANEOUS SYNDROME", "Gastrocutaneous syndrome (disorder)", "peptic Ulcer/hiatal hernia, multiple lentigines/cafe-Au-lait Spots, hypertelorism, myopia", "PEPTIC ULCER/HIATAL HERNIA, MULTIPLE LENTIGINES/CAFE-AU-LAIT SPOTS, HYPERTELORISM, MYOPIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastrocutaneous syndrome", "shortest_name_length": 24}
{"curie": "UMLS:C0013928", "names": ["fat emboli", "Fat emboli", "emboly fat", "fat embolus", "Fat embolus", "embolis fat", "Fat Embolism", "Embolus, fat", "embolism fat", "fat embolism", "FAT EMBOLISM", "Fat embolism", "EMBOLISM, FAT", "fat; embolism", "Embolism, Fat", "embolism; fat", "Fat Embolisms", "Embolisms, Fat", "Fat embolism (disorder)", "fat embolism (diagnosis)", "Fat embolus (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fat embolism (disorder)", "shortest_name_length": 10}
{"curie": "MONDO:0001626", "names": ["Traumatic glaucoma", "Glaucoma traumatic", "traumatic glaucoma", "glaucoma; traumatic", "traumatic; glaucoma", "Glaucoma due to ocular trauma", "glaucoma associated with ocular trauma", "Glaucoma associated with ocular trauma", "Glaucoma associated with ocular trauma (disorder)", "glaucoma associated with ocular trauma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "traumatic glaucoma", "shortest_name_length": 18}
{"curie": "MONDO:0002211", "names": ["B cell deficiency", "B-Cell Deficiency", "B-cell deficiency", "Humoral immune defect", "Humoural immune defect", "Predominantly B-cell defect", "Humoral immunity deficiency", "Humoural immunity deficiency", "B cell (antibody) deficiencies", "deficiency of humoral immunity", "Deficiency of humoral immunity", "Deficiency of Humoral Immunity", "Humoral immune defect (finding)", "immunoglobulin heavy chain deletion", "Other deficiency of humoral immunity", "Immunoglobulin heavy chain deficiency", "immunoglobulin heavy chain deficiency", "Other selective immunoglobulin deficiencies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B cell deficiency", "shortest_name_length": 17}
{"curie": "UMLS:C0349659", "names": ["Bladder Rhabdomyosarcoma", "rhabdomyosarcoma of bladder", "Rhabdomyosarcoma of bladder", "Rhabdomyosarcoma of urinary bladder", "Rhabdomyosarcoma of bladder (disorder)", "rhabdomyosarcoma of bladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rhabdomyosarcoma of bladder", "shortest_name_length": 24}
{"curie": "MONDO:0007393", "names": ["Cranioacrofacial syndrome", "CRANIOACROFACIAL SYNDROME", "Cranioacrofacial Syndrome", "cranioacrofacial syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cranioacrofacial syndrome", "shortest_name_length": 25}
{"curie": "UMLS:C4525305", "names": ["Gallbladder cancer", "stage IV gallbladder cancer", "Stage IV Gallbladder Cancer", "Stage IV Gallbladder Cancer AJCC v8", "stage IV gallbladder cancer AJCC v8", "stage IV gallbladder carcinoma AJCC v8", "Stage IV Gallbladder Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Gallbladder Cancer AJCC v8", "shortest_name_length": 18}
{"curie": "MONDO:0012693", "names": ["GSD0B", "GSD 0B", "GSD 0b", "GSD type 0b", "GSD type 0b (muscle)", "Glycogenosis type 0b", "glycogenosis type 0b", "glycogen storage disease type 0b", "Glycogen storage disease type 0b", "muscle glycogen storage disease 0", "Muscle Glycogen Storage Disease 0", "MUSCLE GLYCOGEN STORAGE DISEASE 0", "GLYCOGEN STORAGE DISEASE 0, MUSCLE", "Glycogen Storage Disease 0, Muscle", "glycogen storage disease 0, muscle", "muscle glycogen synthase deficiency", "MUSCLE GLYCOGEN SYNTHASE DEFICIENCY", "Muscle Glycogen Synthase Deficiency", "glycogen synthetase deficiency type 0b", "glycogen storage disease type 0, muscle", "Muscle and heart glycogen synthase deficiency", "glycogen synthetase deficiency type 0b (diagnosis)", "GSD due to muscle and heart glycogen synthase deficiency", "Muscle and heart glycogen synthase deficiency (disorder)", "glycogenosis due to muscle and heart glycogen synthase deficiency", "Glycogenosis due to muscle and heart glycogen synthase deficiency", "heart glycogen storage disease due to glycogen synthase deficiency", "glycogen storage disease due to glycogen synthase deficiency of heart", "glycogen storage disease due to muscle and heart glycogen synthase deficiency", "Glycogen storage disease due to muscle and heart glycogen synthase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease due to muscle and heart glycogen synthase deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0030116", "names": ["SRS2", "SILVER-RUSSELL SYNDROME 2", "silver-russell syndrome 2", "UNIPARENTAL DISOMY, MATERNAL, CHROMOSOME 7", "Uniparental Disomy, Maternal, Chromosome 7", "Maternal uniparental disomy of chromosome 7", "Maternal uniparental disomy of chromosome 7 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "silver-russell syndrome 2", "shortest_name_length": 4}
{"curie": "MONDO:0005200", "names": ["viral cardiomyopathy", "CARDIOMYOPATHY VIRAL", "Viral cardiomyopathy", "viral dilated cardiomyopathy", "Viruses dilated cardiomyopathy", "Viruses caused dilated cardiomyopathy", "Dilated cardiomyopathy due to viral myocarditis", "Dilated cardiomyopathy secondary to viral myocarditis", "Dilated cardiomyopathy due to viral myocarditis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "viral dilated cardiomyopathy", "shortest_name_length": 20}
{"curie": "MONDO:0018736", "names": ["KLA", "kaposiform lymphangiomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kaposiform lymphangiomatosis", "shortest_name_length": 3}
{"curie": "MONDO:0014785", "names": ["MSSGM2", "microcephaly, short stature, and impaired glucose metabolism 2", "MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2", "microcephaly, short stature, and impaired glucose metabolism type 2", "PPP1R15B microcephaly, short stature, and impaired glucose metabolism", "microcephaly, short stature, and impaired glucose metabolism 2; MSSGM2", "microcephaly, short stature, and impaired glucose metabolism caused by mutation in PPP1R15B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly, short stature, and impaired glucose metabolism 2", "shortest_name_length": 6}
{"curie": "MONDO:0100234", "names": ["IVF", "paroxysmal ventricular fibrillation", "idiopathic ventricular fibrillation", "paroxysmal familial ventricular fibrillation", "ventricular fibrillation, paroxysmal familial", "idiopathic ventricular fibrillation, non Brugada type", "paroxysmal familial ventricular fibrillation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paroxysmal familial ventricular fibrillation", "shortest_name_length": 3}
{"curie": "UMLS:C1519204", "names": ["SMECE", "Sclerosing Mucoepidermoid Thyroid Carcinoma with Eosinophilia", "Sclerosing Mucoepidermoid Thyroid Gland Carcinoma with Eosinophilia", "Thyroid Gland Sclerosing Mucoepidermoid Carcinoma with Eosinophilia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Sclerosing Mucoepidermoid Carcinoma with Eosinophilia", "shortest_name_length": 5}
{"curie": "UMLS:C4744392", "names": ["Sellar Mature Teratoma", "Mature Teratoma of the Sellar Region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sellar Mature Teratoma", "shortest_name_length": 22}
{"curie": "UMLS:C1512438", "names": ["High Grade Prostatic Intraepithelial Neoplasia, Signet Ring Variant", "High Grade Prostatic Intraepithelial Neoplasia, Signet-Ring Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Prostatic Intraepithelial Neoplasia, Signet Ring Variant", "shortest_name_length": 67}
{"curie": "MONDO:0032607", "names": ["VETD", "heterozygotes for TBX2 variants", "vertebral anomalies and variable endocrine and T-cell dysfunction", "VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vertebral anomalies and variable endocrine and T-cell dysfunction", "shortest_name_length": 4}
{"curie": "MONDO:0002919", "names": ["Posterior Fossa Meningioma", "posterior fossa meningioma", "Posterior Fossa Meningiomas", "Meningioma, Posterior Fossa", "Meningiomas, Posterior Fossa", "posterior cranial fossa meningioma", "Posterior Cranial Fossa Meningioma", "Meningioma of Posterior Cranial Fossa", "meningioma of posterior cranial fossa", "Meningioma of the Posterior Cranial Fossa", "meningioma of the Posterior Cranial Fossa", "meningioma of the posterior cranial fossa", "posterior cranial fossa meningioma (disease)", "meningioma (disease) of posterior cranial fossa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "posterior cranial fossa meningioma", "shortest_name_length": 26}
{"curie": "MONDO:0001951", "names": ["seven year itch", "Crusted scabies", "crusted scabies", "scabies norwegian", "norwegian scabies", "Norwegian Scabies", "Norwegian scabies", "itch; Norwegian itch", "Norwegian itch; itch", "Crusted scabies (disorder)", "Norwegian scabies (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Norwegian scabies", "shortest_name_length": 15}
{"curie": "UMLS:C0280380", "names": ["nasopharynx squamous cell carcinoma, stage II", "Nasopharyngeal squamous cell carcinoma stage II", "nasopharyngeal squamous cell carcinoma, stage II", "epidermoid carcinoma of the nasopharynx, stage II", "stage II squamous cell carcinoma of the nasopharynx", "squamous cell carcinoma of the nasopharynx, stage II", "Stage II Keratinizing Epidermoid Carcinoma of Nasopharynx", "Stage II Nasopharyngeal Keratinizing Epidermoid Carcinoma", "Stage II Keratinizing Squamous Cell Carcinoma of Nasopharynx", "Stage II Nasopharyngeal Keratinizing Squamous Cell Carcinoma", "Stage II Keratinizing Epidermoid Carcinoma of the Nasopharynx", "Stage II Keratinizing Squamous Cell Carcinoma of the Nasopharynx", "Stage II Nasopharyngeal Throat Keratinizing Squamous Cell Cancer", "Stage II Nasopharyngeal Keratinizing Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasopharyngeal squamous cell carcinoma stage II", "shortest_name_length": 45}
{"curie": "UMLS:C4520725", "names": ["Stage IV Soft Tissue Sarcoma", "Stage IV Adult Sarcoma of Soft Tissue", "Stage IV Adult Sarcoma of the Soft Tissue", "Stage IV Adult Soft Tissue Sarcoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Adult Soft Tissue Sarcoma AJCC v7", "shortest_name_length": 28}
{"curie": "MONDO:0012107", "names": ["neuropathy, hereditary sensory and autonomic, adult-onset, with anosmia", "NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, ADULT-ONSET, WITH ANOSMIA", "Neuropathy, Hereditary Sensory and Autonomic, Adult-Onset, with Anosmia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuropathy, hereditary sensory and autonomic, adult-onset, with anosmia", "shortest_name_length": 71}
{"curie": "UMLS:C0752287", "names": ["Intrinsic Sleep Disorder", "Sleep Disorder, Intrinsic", "Intrinsic Sleep Disorders", "Sleep Disorders, Intrinsic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sleep Disorders, Intrinsic", "shortest_name_length": 24}
{"curie": "MONDO:0009850", "names": ["Adult Periodontitis", "Adult periodontitis", "periodontitis, adult", "PERIODONTITIS, ADULT", "Periodontitis, Adult", "Chronic Periodontitis", "Adult Periodontitides", "Chronic periodontitis", "chronic periodontitis", "PERIODONTITIS, CHRONIC", "chronic pericementitis", "Periodontitis, Chronic", "Chronic pericementitis", "periodontitis, chronic", "Periodontitides, Adult", "Chronic Periodontitides", "Periodontitides, Chronic", "Adult-onset periodontitis", "Chronic periodontal disease", "periodontitis, chronic, adult", "Chronic periodontitis (disorder)", "chronic periodontitis (diagnosis)", "chronic pericementitis (diagnosis)", "Chronic periodontitis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "periodontitis, chronic, adult", "shortest_name_length": 19}
{"curie": "MONDO:0015730", "names": ["trisomy 17", "Trisomy 17", "mosaic trisomy 17", "Mosaic trisomy 17", "trisomy 17 mosaicism", "Trisomy 17 mosaicism", "chromosome 17 trisomy", "Chromosome 17 trisomy", "Mosaic trisomy type 17", "chromosome 17, trisomy", "Chromosome 17 duplication", "chromosome 17 duplication", "Mosaic trisomy 17 syndrome", "Mosaic trisomy chromosome 17", "chromosome 17, trisomy mosaicism", "trisomy 17 mosaicism (diagnosis)", "Mosaic trisomy 17 syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mosaic trisomy 17", "shortest_name_length": 10}
{"curie": "OMIM:614745", "names": [], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"]}
{"curie": "UMLS:C5206595", "names": ["Paratesticular Mesenchymal Neoplasm", "Paratesticular Soft Tissue Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paratesticular Soft Tissue Neoplasm", "shortest_name_length": 35}
{"curie": "MONDO:0006097", "names": ["ALT", "ALT/WDLPS", "Atypical Lipoma", "Atypical lipoma", "Atypical Lipomas", "Lipoma, Atypical", "Lipomas, Atypical", "lipoma-like liposarcoma", "Lipoma-like liposarcoma", "Atypical lipomatous tumor", "Atypical Lipomatous Tumor", "atypical lipomatous tumor", "Atypical lipomatous tumour", "Liposarcoma, differentiated", "Well-Differentiated Liposarcoma", "well differentiated liposarcoma", "Well Differentiated Liposarcoma", "well-differentiated liposarcoma", "Liposarcoma, well differentiated", "Atypical lipoma (morphologic abnormality)", "superficial well differentiated liposarcoma", "Atypical Lipomatous Tumor/Well-Differentiated Liposarcoma", "Atypical Lipomatous Tumor/Well Differentiated Liposarcoma", "liposarcoma, well differentiated (morphologic abnormality)", "well differentiated liposarcoma of superficial soft tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical lipomatous tumor", "shortest_name_length": 3}
{"curie": "MONDO:0007922", "names": ["LPHDST", "lymphedema with distichiasis", "LYMPHEDEMA WITH DISTICHIASIS", "Lymphedema with distichiasis", "LYMPHEDEMA-DISTICHIASIS SYNDROME", "Lymphedema distichiasis syndrome", "Lymphedema-Distichiasis Syndrome", "Distichiasis-lymphedema syndrome", "Lymphedema-distichiasis syndrome", "lymphedema-distichiasis syndrome", "Distichiasis-lymphoedema syndrome", "Distichiasis-lymphedema syndrome (disorder)", "Hereditary lymphedema-distichiasis syndrome", "hereditary lymphedema-distichiasis syndrome (subtype)", "Lymphedema-Distichiasis Syndrome with Renal Disease and Diabetes Mellitus", "lymphedema-distichiasis syndrome with renal disease and diabetes mellitus", "LYMPHEDEMA-DISTICHIASIS SYNDROME WITH RENAL DISEASE AND DIABETES MELLITUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphedema-distichiasis syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C4287999", "names": ["Vulvar SIL", "Vulvar Squamous Intraepithelial Lesion", "Vulvar Intraepithelial Neoplasia, HPV-Associated", "Vulvar Squamous Intraepithelial Lesion, HPV-Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Squamous Intraepithelial Lesion, HPV-Associated", "shortest_name_length": 10}
{"curie": "UMLS:C0376280", "names": ["Neurotic Anxiety State", "Anxiety State, Neurotic", "State, Neurotic Anxiety", "Neurotic Anxiety States", "Anxiety state, neurotic", "States, Neurotic Anxiety", "Anxiety States, Neurotic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anxiety States, Neurotic", "shortest_name_length": 22}
{"curie": "UMLS:C0346184", "names": ["Benign Ovarian Germ Cell Tumor", "benign germ cell tumor of ovary", "Benign Ovarian Germ Cell Tumors", "Benign germ cell tumor of ovary", "Benign Germ Cell Tumor of Ovary", "Benign germ cell tumour of ovary", "Ovarian Germ Cell Tumors, Benign", "Benign Ovarian Germ Cell Neoplasm", "Germ Cell Tumors, Ovarian, Benign", "Benign Germ Cell Neoplasm of Ovary", "Benign Ovarian Germ Cell Neoplasms", "Ovarian Germ Cell Neoplasms, Benign", "Benign Germ Cell Tumor of the Ovary", "Germ Cell Neoplasms, Ovarian, Benign", "Benign Germ Cell Neoplasm of the Ovary", "ovarian neoplasm benign germ cell tumor", "Benign germ cell tumor of ovary (disorder)", "benign germ cell tumor of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign germ cell tumor of ovary", "shortest_name_length": 30}
{"curie": "MONDO:0016346", "names": ["Sengers-Hamel-Otten syndrome", "Sengers Hamel Otten syndrome", "hydrocephalus obesity hypogonadism", "Hydrocephalus-obesity-hypogonadism syndrome", "hydrocephalus-obesity-hypogonadism syndrome", "Hydrocephalus with obesity and hypogonadism syndrome", "Hydrocephalus with obesity and hypogonadism syndrome (disorder)", "congenital hydrocephalus oligophrenia dwarfism centripetal obesity and hypogonadism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hydrocephalus-obesity-hypogonadism syndrome", "shortest_name_length": 28}
{"curie": "UMLS:C1735322", "names": ["Injection site pallor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site pallor", "shortest_name_length": 21}
{"curie": "UMLS:C0334572", "names": ["Fibrodentinoma", "Ameloblastic Fibroma", "Ameloblastic fibroma", "fibroma; ameloblastic", "ameloblastic; fibroma", "Ameloblastic fibroma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ameloblastic fibroma", "shortest_name_length": 14}
{"curie": "MONDO:0005582", "names": ["Binges", "bulimia", "Bulimia", "BULIMIA", "Bingeing", "Bulimias", "Bulimia NOS", "Binge eating", "Binge Eating", "binge eating", "Eating, Binge", "Binge and purge", "Binge overeating", "bulimic episodes", "Bouts of overeating", "hyperorexia nervosa", "Hyperorexia nervosa", "Binge eating disorder", "binge-eating disorder", "Binge Eating Disorder", "binge eating disorder", "Binge-Eating Disorder", "binge disorder eating", "Binge-eating disorder", "eating disorder binge", "Binge-Eating Disorders", "Episodes of overeating", "Disorder, Binge-Eating", "binge disorders eating", "Disorders, Binge-Eating", "Binge eating disorder (disorder)", "Binge eating disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "binge eating disorder", "shortest_name_length": 6}
{"curie": "MONDO:0021484", "names": ["Benign Maxillary Sinus Tumor", "benign maxillary sinus tumor", "benign maxillary antrum tumor", "benign tumor of maxillary sinus", "benign maxillary sinus neoplasm", "Benign tumor of maxillary sinus", "Benign Tumor of Maxillary Sinus", "Benign Maxillary Sinus Neoplasm", "maxillary sinus benign neoplasm", "benign tumor of maxillary antrum", "Benign tumor of maxillary antrum", "benign maxillofacial sinus tumor", "Benign tumour of maxillary sinus", "benign maxillary antrum neoplasm", "Benign tumour of maxillary antrum", "Benign neoplasm of maxillary sinus", "benign neoplasm of maxillary sinus", "Benign Neoplasm of Maxillary Sinus", "benign maxillofacial sinus neoplasm", "benign tumor of the maxillary sinus", "benign neoplasm of maxillary antrum", "Benign Tumor of the Maxillary Sinus", "benign tumor of maxillofacial sinus", "benign tumor of the maxillary antrum", "benign neoplasm of the maxillary sinus", "Benign Neoplasm of the Maxillary Sinus", "benign neoplasm of maxillofacial sinus", "benign tumor of the maxillofacial sinus", "benign neoplasm of the maxillary antrum", "benign neoplasm of the maxillofacial sinus", "Benign neoplasm of maxillary sinus (disorder)", "benign neoplasm of maxillary sinus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of maxillary sinus", "shortest_name_length": 28}
{"curie": "MONDO:0003708", "names": ["Extrahepatic Bile Duct Small Cell NEC", "extrahepatic bile duct small cell NEC", "Oat cell extrahepatic bile duct carcinoma", "Oat Cell Extrahepatic Bile Duct Carcinoma", "Extrahepatic Bile Duct Small Cell Carcinoma", "Small Cell Extrahepatic Bile Duct Carcinoma", "small cell extrahepatic bile duct carcinoma", "Oat cell carcinoma of extrahepatic bile duct", "Oat Cell Carcinoma of Extrahepatic Bile Duct", "small cell carcinoma of extrahepatic bile duct", "extrahepatic bile duct small cell adenocarcinoma", "Oat Cell Carcinoma of the Extrahepatic Bile Duct", "Oat cell carcinoma of the extrahepatic bile duct", "small cell adenocarcinoma of extrahepatic bile duct", "Small Cell Adenocarcinoma of Extrahepatic Bile Duct", "Small Cell Adenocarcinoma of the Extrahepatic Bile Duct", "small cell adenocarcinoma of the extrahepatic bile duct", "Extrahepatic Bile Duct Small Cell Neuroendocrine Carcinoma", "Small Cell Extrahepatic Bile Duct Neuroendocrine Carcinoma", "small cell carcinoma of extrahepatic bile duct (diagnosis)", "small cell extrahepatic bile duct neuroendocrine carcinoma", "extrahepatic bile duct small cell neuroendocrine carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extrahepatic bile duct small cell adenocarcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0023671", "names": ["OPDM3", "oculopharyngodistal myopathy 3", "OCULOPHARYNGODISTAL MYOPATHY 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculopharyngodistal myopathy 3", "shortest_name_length": 5}
{"curie": "MONDO:0022781", "names": ["cleft lip palate-tetraphocomelia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleft lip palate-tetraphocomelia", "shortest_name_length": 32}
{"curie": "UMLS:C1699736", "names": ["Kidney anastomotic leak", "anastomotic leak kidney", "Kidney Anastomotic Leakage", "Kidney anastomotic leak (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kidney Anastomotic Leakage", "shortest_name_length": 23}
{"curie": "UMLS:C5418862", "names": ["Acral Edema", "Edema of the palms and/or soles"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acral Edema", "shortest_name_length": 11}
{"curie": "MONDO:0016877", "names": ["partial deletion of chromosome 12q", "partial monosomy of chromosome 12q", "partial deletion of the long arm of chromosome 12", "partial monosomy of the long arm of chromosome 12", "partial deletion of the long arm of chromosome type 12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of the long arm of chromosome 12", "shortest_name_length": 34}
{"curie": "MONDO:0011625", "names": ["DFNA18", "autosomal dominant deafness 18", "Deafness, Autosomal Dominant 18", "deafness, autosomal dominant 18", "DEAFNESS, AUTOSOMAL DOMINANT 18", "DEAFNESS, AUTOSOMAL DOMINANT 18 (disorder)", "autosomal dominant nonsyndromic deafness 18", "autosomal dominant nonsyndromic hearing loss 18", "autosomal dominant nonsyndromic deafness type 18"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 18", "shortest_name_length": 6}
{"curie": "MONDO:0014196", "names": ["HRTFDS", "Hartsfield Syndrome", "HARTSFIELD SYNDROME", "HARTSFIELD syndrome", "Hartsfield syndrome", "Hartsfield Bixler Demyer syndrome", "Hartsfield-Bixler-Demyer syndrome", "Holoprosencephaly-ectrodactyly-cleft lip/palate syndrome", "holoprosencephaly-ectrodactyly-cleft lip palate syndrome", "holoprosencephaly-ectrodactyly-cleft lip/palate syndrome", "HOLOPROSENCEPHALY, ECTRODACTYLY, AND BILATERAL CLEFT LIP/PALATE", "holoprosencephaly, ectrodactyly, and bilateral cleft Lip/palate", "Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip-Palate", "Holoprosencephaly, ectrodactyly, cleft lip, cleft palate syndrome", "Holoprosencephaly, ectrodactyly, cleft lip, cleft palate syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hartsfield-Bixler-Demyer syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0004928", "names": ["lymph node disease", "disease lymph nodes", "Lymph node disorder", "diseases lymph node", "Lymph Node Disorder", "lymph node disorder", "disorders lymph node", "disease of lymph node", "Lymph nodes--Diseases", "disorder of lymph node", "Disorder of lymph node", "lymphatic glands (nodes)", "Disease of lymph node, NOS", "DISEASES OF THE LYMPH NODES", "lymph node disease or disorder", "disease or disorder of lymph node", "Disorder of lymph node (disorder)", "disorder of lymph node (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymph node disorder", "shortest_name_length": 18}
{"curie": "MONDO:0008429", "names": ["SGMRT1", "SM syndrome", "Singleton-Merten Syndrome", "Merten-Singleton syndrome", "Singleton Merten syndrome", "singleton Merten syndrome", "Singleton-Merten syndrome", "Singleton-Merten dysplasia", "Singleton-Merten syndrome (disorder)", "widened medullary cavities of bone, aortic calcification, abnormal dentition, and muscular weakness", "syndrome of widened medullary cavities of the metacarpals and phalanges, aortic calcification and abnormal dentition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Singleton-Merten dysplasia", "shortest_name_length": 6}
{"curie": "MONDO:0013505", "names": ["SPGF9", "globozoospermia", "DPY19L2 azoospermia", "Globozoospermia, total", "GLOBOZOOSPERMIA, TOTAL", "globozoospermia, total", "spermatogenic failure 9", "SPERMATOGENIC FAILURE 9", "globozoospermia, complete", "GLOBOZOOSPERMIA, COMPLETE", "spermatogenic failure type 9", "male infertility due to globozoospermia", "azoospermia caused by mutation in DPY19L2", "male infertility due to round-headed spermatozoa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 9", "shortest_name_length": 5}
{"curie": "MONDO:0015429", "names": ["CHM-hypopituitarism syndrome", "choroideremia-hypopituitarism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choroideremia-hypopituitarism syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0014874", "names": ["PCH2F", "pontocerebellar hypoplasia type 2F", "pontocerebellar hypoplasia, type 2F", "PONTOCEREBELLAR HYPOPLASIA, TYPE 2F", "pontocerebellar hypoplasia, type 2F; PCH2F", "TSEN15 non-syndromic pontocerebellar hypoplasia", "non-syndromic pontocerebellar hypoplasia caused by mutation in TSEN15"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pontocerebellar hypoplasia, type 2F", "shortest_name_length": 5}
{"curie": "MONDO:0004896", "names": ["cross-eye", "cross eye", "Esotropia", "ESOTROPIA", "Cross-Eye", "esotropia", "Cross-eye", "Cross Eye", "esotropias", "Esotropia,", "Esotropias", "Cross-Eyes", "cross eyes", "eyes cross", "crossed eye", "crossed eyes", "crossing eye", "Crossed Eyes", "esodeviation", "crossing eyes", "Esotropia, NOS", "crossings eyes", "eyes are crossed", "Convergent squint", "convergent squint", "Internal strabismus", "internal strabismus", "disorders esotropia", "Internal Strabismus", "Strabismus, Internal", "Esotropia (disorder)", "esotropia (diagnosis)", "Convergent strabismus", "Convergent Strabismus", "Unspecified esotropia", "Esotropia, unspecified", "convergent; strabismus", "Strabismus, Convergent", "strabismus; convergent", "Inward turning cross eyed", "Manifest convergent squint", "eyes are crossed (symptom)", "Constant comitant esotropia", "convergence in manifest squint", "Convergence in manifest squint", "Convergent concomitant strabismus", "strabismus; concomitant, convergent", "concomitant; strabismus, convergent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esotropia", "shortest_name_length": 9}
{"curie": "UMLS:C5420188", "names": ["Benign Laryngeal Soft Tissue Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Laryngeal Soft Tissue Neoplasm", "shortest_name_length": 37}
{"curie": "MONDO:0014243", "names": ["PWLS", "SHFYNG", "PWS-like", "MAGEL2-related PWLS", "Schaaf-Yang syndrome", "Schaaf Yang syndrome", "SCHAAF-YANG SYNDROME", "Chitayat-Hall syndrome", "CHITAYAT-HALL SYNDROME", "PRADER-WILLI-LIKE SYNDROME", "Prader-Willi-like syndrome", "PWS due to a point mutation", "Prader-Willi-like syndrome (disorder)", "MAGEL2-related Prader-Willi-like syndrome", "Prader-Willi syndrome due to point mutation", "MAGE family member L2-related Prader-Willi-like syndrome", "MAGE family member L2-related Prader-Willi-like syndrome (disorder)", "arthrogryposis, distal, with hypopituitarism, mental retardation, and facial anomalies", "Arthrogryposis, distal, with hypopituitarism, mental retardation, and facial anomalies", "ARTHROGRYPOSIS, DISTAL, WITH HYPOPITUITARISM, MENTAL RETARDATION, AND FACIAL ANOMALIES", "distal arthrogryposis with hypopituitarism, intellectual disability and facial anomalies", "arthrogryposis, distal, with hypopituitarism, intellectual disability, and facial anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Schaaf-Yang syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0010406", "names": ["MRX17", "MRX31", "X-linked mental retardation 31", "X-linked mental retardation 17", "mental retardation, X-linked 17", "MENTAL RETARDATION, X-LINKED 31", "Mental Retardation, X-Linked 17", "mental retardation, X-linked 31", "MENTAL RETARDATION, X-LINKED 17", "Mental Retardation, X-Linked 31", "Xp11.22 microduplication syndrome", "intellectual disability, X-linked 31", "intellectual disability, X-linked 17", "Xp11.22-linked intellectual disability", "CHROMOSOME Xp11.22 DUPLICATION SYNDROME", "chromosome Xp11.22 duplication syndrome", "X-linked mental retardation 31 (MRX31, XLMR31)", "X-linked mental retardation 17 (MRX17, XLMR17)", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 17"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome Xp11.22 duplication syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0029131", "names": ["PNRIID", "peripheral neuropathy, autosomal recessive, with or without impaired intellectual development", "PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peripheral neuropathy, autosomal recessive, with or without impaired intellectual development", "shortest_name_length": 6}
{"curie": "MONDO:0001084", "names": ["primary optic atrophy", "Primary optic atrophy", "Primary optic atrophy (disorder)", "primary optic atrophy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary optic atrophy", "shortest_name_length": 21}
{"curie": "UMLS:C5420390", "names": ["Non-Neoplastic Tonsillar Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Tonsillar Disorder", "shortest_name_length": 33}
{"curie": "UMLS:C5239030", "names": ["Metastatic Malignant Neoplasm in the Digestive System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Malignant Neoplasm in the Digestive System", "shortest_name_length": 53}
{"curie": "UMLS:C5420081", "names": ["Sinonasal Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor", "shortest_name_length": 66}
{"curie": "UMLS:C5418785", "names": ["Lower Alveolar Ridge Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lower Alveolar Ridge Squamous Cell Carcinoma", "shortest_name_length": 44}
{"curie": "MONDO:0015564", "names": ["GLNH", "AFLH", "ALNH", "Castleman Tumor", "castlemans tumor", "Castlemans Tumor", "Castleman Disease", "CASTLEMAN DISEASE", "Castleman's tumor", "Castleman's Tumor", "castleman disease", "Castleman disease", "castleman's tumor", "Castlemans Disease", "castlemans disease", "Tumor, Castleman's", "lymphoid hamartoma", "castleman's disease", "Disease, Castlemans", "Castleman's disease", "Castleman's Disease", "Angiolymphoid hyperplasia", "angiolymphoid hyperplasia", "Giant lymph node hyperplasia", "Giant Lymph Node Hyperplasia", "giant lymph node hyperplasia", "Lymph Node Hyperplasia, Giant", "Hyperplasia, Giant Lymph Node", "Castleman's disease (disorder)", "Angiomatous lymphoid hamartoma", "Castleman's disease (diagnosis)", "angiofollicular lymph hyperplasia", "Angiofollicular Lymph Hyperplasia", "Angiofollicular lymph hyperplasia", "Benign angiofollicular hyperplasia", "Angiofollicular Lymph Hyperplasias", "Lymph Hyperplasia, Angiofollicular", "Hyperplasia, Angiofollicular Lymph", "angiofollicular lymphoid hyperplasia", "Angiofollicular Lymphoid Hyperplasia", "Lymphoid Hyperplasia, Angiofollicular", "Angiofollicular Lymphoid Hyperplasias", "Hyperplasia, Angiofollicular Lymphoid", "Angiofollicular ganglionic hyperplasia", "Angiofollicular lymph node hyperplasia", "angiofollicular lymph node hyperplasia", "Angiofollicular Lymph Node Hyperplasia", "angiofollicular ganglionic hyperplasia", "Angiofollicular lymph node hyperplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Castleman disease", "shortest_name_length": 4}
{"curie": "MONDO:0007079", "names": ["alcoholism", "Dipsomania", "dipsomania", "ALCOHOLISM", "Alcoholism", "alcoholisms", "Alcoholism, NOS", "ETOH dependence", "Alcohol addiction", "Alcohol Addiction", "addiction alcohol", "Addiction;alcohol", "alcohol addiction", "Alcoholism;chronic", "alcohol dependence", "addiction; alcohol", "ALCOHOL DEPENDENCE", "alcoholism chronic", "Dependence;alcohol", "alcohol; addiction", "Alcohol Dependence", "Alcohol dependence", "Addiction, Alcohol", "ALCOHOLISM CHRONIC", "chronic alcoholism", "Alcohol dependency", "alcohol dependency", "Addiction, alcohol", "Chronic alcoholism", "addicted to alcohol", "disorder alcoholism", "dependence; alcohol", "alcohol dependences", "Alcoholism, chronic", "alcohol; dependence", "Dependence, Alcohol", "drunkenness; chronic", "chronic; drunkenness", "alcoholism disorders", "ALCOHOL ABUSE CHRONIC", "chronic alcohol abuse", "Chronic alcohol abuse", "Abuse;alcohol;chronic", "Alcoholism (disorder)", "Dependency on alcohol", "Alcohol abuse chronic", "alcohol abuse alcoholism", "alcoholism/alcohol abuse", "abuse alcohol alcoholism", "Persistent alcohol abuse", "Alcohol problem drinking", "dependence; ethyl alcohol", "ethyl alcohol; dependence", "alcohol dependence syndrome", "obsolete_alcohol dependence", "Alcohol dependence syndrome", "Intoxication;alcohol;chronic", "alcoholism chronic disorders", "chronic alcohol intoxication", "Alcohol dependence (disorder)", "dependence alcoholism alcohol", "Alcoholic dependence syndrome", "alcohol dependence (diagnosis)", "Chronic Alcoholic Intoxication", "Intoxication, Chronic Alcoholic", "Alcoholic Intoxication, Chronic", "Alcoholism with alcohol dependence", "Persistent alcohol abuse (disorder)", "Persistent alcohol abuse (diagnosis)", "alcohol dependence, susceptibility to", "alcohol dependence, protection against", "Alcohol abuse, continuous drinking behavior", "Alcohol abuse, continuous drinking behaviour", "Mental and behavioral disorders due to use of alcohol, dependence syndrome", "Mental and behavioural disorders due to use of alcohol, dependence syndrome", "AERODIGESTIVE TRACT CANCER, SQUAMOUS CELL, ALCOHOL-RELATED, PROTECTION AGAINST", "aerodigestive tract cancer, squamous cell, alcohol-related, protection against"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alcohol dependence", "shortest_name_length": 10}
{"curie": "UMLS:C1336301", "names": ["Stage 2 Neuroblastoma", "stage 2 neuroblastoma", "Stage II Neuroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 2 Neuroblastoma", "shortest_name_length": 21}
{"curie": "UMLS:C0494698", "names": ["odontogenesis; disorder", "disorder; odontogenesis", "tooth development disorder", "Abnormal tooth development", "disturbance; odontogenesis", "Abnormal Tooth Development", "Tooth development disorder", "Tooth Development Disorder", "Dental Developmental Disorder", "tooth; developmental disorder", "Disorder of odontogenesis NOS", "Disorder of tooth development", "dental disorders tooth development", "disease (or disorder); odontogenesis", "Disorder of tooth development (disorder)", "Disorder of tooth development (diagnosis)", "Disorder of tooth development, unspecified", "disease (or disorder); tooth, teeth, development"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dental Developmental Disorder", "shortest_name_length": 23}
{"curie": "UMLS:C3495916", "names": ["Myocardial Hypertrophy", "Myocardial hypertrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myocardial hypertrophy", "shortest_name_length": 22}
{"curie": "MONDO:0008570", "names": ["TTPP1", "CACNA1S thyrotoxic periodic paralysis", "thyrotoxic periodic paralysis, susceptibility to, 1", "THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 1", "thyrotoxic periodic paralysis, susceptibility to, type 1", "thyrotoxic periodic paralysis caused by mutation in CACNA1S"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyrotoxic periodic paralysis, susceptibility to, 1", "shortest_name_length": 5}
{"curie": "UMLS:C0001338", "names": ["Herpetic acute necrotizing encephalitis", "Herpetic Acute Necrotizing Encephalitis", "Herpetic acute necrotising encephalitis", "Acute necrotizing encephalitis, herpetic", "Acute Necrotizing Encephalitis, Herpetic", "Herpetic acute necrotizing encephalitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Herpetic Acute Necrotizing Encephalitis", "shortest_name_length": 39}
{"curie": "MONDO:0013985", "names": ["DFNB18B", "autosomal recessive deafness 18B", "DEAFNESS, AUTOSOMAL RECESSIVE 18B", "deafness, autosomal recessive 18b", "deafness, autosomal recessive 18B", "deafness, autosomal recessive type 18B", "autosomal recessive nonsyndromic deafness 18B", "OTOG autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 18B", "autosomal recessive nonsyndromic deafness type 18B", "autosomal recessive nonsyndromic deafness caused by mutation in OTOG"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 18B", "shortest_name_length": 7}
{"curie": "MONDO:0004204", "names": ["Dyskeratotic Skin Papilloma", "Dyskeratotic skin papilloma", "parakeratotic skin papilloma", "Parakeratotic Skin Papilloma", "Parakeratotic skin papilloma", "Squamous Cell Skin Papilloma", "squamous cell skin papilloma", "Skin Squamous Cell Papilloma", "hyperkeratotic skin papilloma", "Hyperkeratotic Skin Papilloma", "Dyskeratotic papilloma of skin", "Dyskeratotic Papilloma of Skin", "parakeratotic papilloma of skin", "squamous cell papilloma of skin", "Parakeratotic papilloma of skin", "Parakeratotic Papilloma of Skin", "Squamous Cell Papilloma of Skin", "zone of skin squamous papilloma", "Squamous cell papilloma of skin", "Hyperkeratotic papilloma of skin", "hyperkeratotic papilloma of skin", "Hyperkeratotic Papilloma of Skin", "Dyskeratotic papilloma of the skin", "Dyskeratotic Papilloma of the Skin", "Parakeratotic Papilloma of the Skin", "Squamous Cell Papilloma of the Skin", "parakeratotic papilloma of the skin", "squamous cell papilloma of the skin", "hyperkeratotic papilloma of the skin", "Hyperkeratotic Papilloma of the Skin", "Squamous cell papilloma of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "squamous cell skin papilloma", "shortest_name_length": 27}
{"curie": "MONDO:0007629", "names": ["fragile site 10Q23", "FRAGILE SITE 10q23", "fragile site type 10Q23"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fragile site 10Q23", "shortest_name_length": 18}
{"curie": "UMLS:C0857035", "names": ["acute anaphylaxis", "Acute anaphylaxis", "acute anaphylactic reaction", "Acute anaphylactic reaction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute anaphylactic reaction", "shortest_name_length": 17}
{"curie": "UMLS:C0275804", "names": ["Tonsillitis streptococcal", "Streptococcal tonsillitis", "tonsillitis streptococcal", "streptococcal tonsillitis", "streptoccocal; tonsillitis", "tonsillitis; streptoccocal", "Streptococcal tonsillitis (disorder)", "Streptococcal tonsillitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Streptococcal tonsillitis", "shortest_name_length": 25}
{"curie": "MONDO:0024251", "names": ["Minimata disease", "Minamata Disease", "minamata disease", "Minamata disease", "minimata disease", "Chisso-Minamata disease", "Minamata disease (disorder)", "Minamata disease (diagnosis)", "Toxic effect of alkyl mercury compound", "Toxic effect of alkyl mercury compounds"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Minamata disease", "shortest_name_length": 16}
{"curie": "MONDO:0004822", "names": ["Bronchiectasis", "bronchiectases", "BRONCHIECTASIS", "Bronchiectases", "bronchiectasis", "Bronchi dilated", "Bronchiectasis NOS", "bronchiectasis nos", "Bronchiectasis, NOS", "Bronchiectasis (disorder)", "Polynesian bronchiectasis", "bronchiectasis (diagnosis)", "Chronic dilatation of bronchus and bronchiole", "Permanent enlargement of the airways of the lungs"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bronchiectasis", "shortest_name_length": 14}
{"curie": "UMLS:C3267129", "names": ["Prerenal failure", "Prerenal insufficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prerenal failure", "shortest_name_length": 16}
{"curie": "MONDO:0022818", "names": ["congenital aneurysms of the great vessels"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital aneurysms of the great vessels", "shortest_name_length": 41}
{"curie": "MONDO:0005206", "names": ["Renal Cancer", "renal cancer", "Kidney Cancer", "Kidney cancer", "kidney cancer", "RENAL CARCINOMA", "renal carcinoma", "Renal carcinoma", "Renal Carcinoma", "kidney carcinoma", "CARCINOMA KIDNEY", "Carcinoma kidney", "KIDNEY CARCINOMA", "Kidney Carcinoma", "Kidney carcinoma", "Kidney cancer, NOS", "carcinoma of kidney", "Carcinoma of kidney", "CARCINOMA OF KIDNEY", "kidney (renal) cancer", "carcinoma of kidney (diagnosis)", "Kidney (including Renal Cell) Cancer", "kidney (including renal cell) cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal carcinoma", "shortest_name_length": 12}
{"curie": "MONDO:0700120", "names": ["BAFopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "BAFopathy", "shortest_name_length": 9}
{"curie": "MONDO:0044203", "names": ["FVH", "foveal hypoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "foveal hypoplasia", "shortest_name_length": 3}
{"curie": "UMLS:C2697638", "names": ["Hypodiploid ALL", "Hypodiploid Acute Lymphoblastic Leukemia", "Hypodiploid B-Acute Lymphoblastic Leukemia", "Hypodiploid B Acute Lymphoblastic Leukemia", "Hypodiploid B-Cell Acute Lymphoblastic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypodiploid B Acute Lymphoblastic Leukemia", "shortest_name_length": 15}
{"curie": "UMLS:C2826059", "names": ["NK-ALL/LBL", "NK Lymphoblastic Leukemia/Lymphoma", "NK-Lymphoblastic Leukemia/Lymphoma", "NK-lymphoblastic leukemia/lymphoma", "NK-lymphoblastic leukaemia/lymphoma", "Natural killer lymphoblastic leukemia", "Natural killer lymphoblastic leukaemia", "NK Cell Lymphoblastic Leukemia/Lymphoma", "Natural killer-lymphoblastic leukemia/lymphoma", "Natural killer-lymphoblastic leukaemia/lymphoma", "Precursor NK Cell Lymphoblastic Leukemia/Lymphoma", "Natural Killer Cell Lymphoblastic Leukemia/Lymphoma", "Natural killer-lymphoblastic leukemia/lymphoma (disorder)", "Precursor Natural Killer Cell Lymphoblastic Leukemia/Lymphoma", "Natural killer-lymphoblastic leukemia/lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "NK-lymphoblastic leukemia/lymphoma", "shortest_name_length": 10}
{"curie": "EFO:0009277", "names": ["supraventricular ectopy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "supraventricular ectopy", "shortest_name_length": 23}
{"curie": "MONDO:0006426", "names": ["spinal cord PNET", "Spinal Cord PNET", "Spinal Cord Embryonal Tumor, NOS", "Spinal Cord Primitive Neuroectodermal Tumor", "spinal cord primitive neuroectodermal tumor", "primitive neuroectodermal tumor of spinal cord", "Spinal Cord Primitive Neuroectodermal Neoplasm", "Primitive Neuroectodermal Tumor of Spinal Cord", "spinal cord primitive neuroectodermal neoplasm", "primitive neuroectodermal neoplasm of spinal cord", "Primitive Neuroectodermal Neoplasm of Spinal Cord", "Primitive Neuroectodermal Tumor of the Spinal Cord", "primitive neuroectodermal tumor of the spinal cord", "Spinal Cord Embryonal Tumor, Not Otherwise Specified", "primitive neuroectodermal tumor (PNET) of spinal cord", "Primitive Neuroectodermal Neoplasm of the Spinal Cord", "primitive neuroectodermal neoplasm of the spinal cord", "primitive neuroectodermal tumor (PNET) of spinal cord (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal cord primitive neuroectodermal tumor", "shortest_name_length": 16}
{"curie": "MONDO:0003437", "names": ["Occult Small Cell Lung Carcinoma", "occult small cell lung carcinoma", "lung occult small cell carcinoma", "Occult Lung Small Cell Carcinoma", "Occult Small Cell Carcinoma of Lung", "occult small cell carcinoma of lung", "Occult Small Cell Carcinoma of the Lung", "Occult small cell carcinoma of the lung", "occult small cell carcinoma of the lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "occult small cell lung carcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C0577691", "names": ["Disseminated Squamous Cell Carcinoma", "Disseminated squamous cell carcinoma", "Disseminated squamous cell carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disseminated squamous cell carcinoma", "shortest_name_length": 36}
{"curie": "MONDO:0018152", "names": ["geographic choroiditis", "Serpiginous Choroiditis", "choroiditis serpiginous", "serpiginous choroiditis", "Serpiginous choroiditis", "Choroiditis, Serpiginous", "Serpiginous Choroidopathy", "Serpiginous choroidopathy", "serpiginous choroidopathy", "peripapillary choriopathy", "Serpiginous Choroiditides", "Choroidopathy, Serpiginous", "Serpiginous Choroidopathies", "Serpiginous choroidal dystrophy", "Serpiginous choroiditis (disorder)", "geographic serpiginous choroiditis", "Serpiginous choroiditis (diagnosis)", "Geographic helicoid peripapillary choroidopathy", "geographic helicoid peripapillary choroidopathy", "geographic helicoid peripapillary choroidopathy (GHPC)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "serpiginous choroiditis", "shortest_name_length": 22}
{"curie": "MONDO:0009804", "names": ["Oi3", "OI3", "OI type 3", "OI, type 3", "OI type III", "OI, TYPE III", "progressively deforming OI", "Osteogenesis imperfecta III", "OI3 Osteogenesis imperfecta 3", "severe osteogenesis imperfecta", "osteogenesis imperfecta type 3", "Severe osteogenesis imperfecta", "Osteogenesis imperfecta type 3", "Osteogenesis imperfecta, type 3", "osteogenesis imperfecta, type 3", "Osteogenesis imperfecta type III", "osteogenesis imperfecta type III", "Osteogenesis Imperfecta Type III", "Osteogenesis imperfecta, type III", "osteogenesis imperfecta, type III", "OSTEOGENESIS IMPERFECTA, TYPE III", "Osteogenesis Imperfecta, Type III", "OI, type 3 Osteogenesis imperfecta, type 3", "Osteogenesis imperfecta type III (disorder)", "osteogenesis imperfecta type III (diagnosis)", "Progressive deforming osteogenesis imperfecta", "progressive deforming osteogenesis imperfecta", "OI, type III Osteogenesis imperfecta, type III", "progressively deforming osteogenesis imperfecta with normal sclera", "Progressively deforming osteogenesis imperfecta with normal sclerae", "osteogenesis imperfecta, progressively deforming with normal sclerae", "Osteogenesis imperfecta with progressive deformity and normal sclerae", "OSTEOGENESIS IMPERFECTA, PROGRESSIVELY DEFORMING, WITH NORMAL SCLERAE", "Osteogenesis imperfecta, progressively deforming, with normal sclerae", "osteogenesis imperfecta, progressively deforming, with normal sclerae"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteogenesis imperfecta type 3", "shortest_name_length": 3}
{"curie": "UMLS:C4744383", "names": ["Pituitary Gland Non-Hodgkin Lymphoma", "Primary Pituitary Gland Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pituitary Gland Non-Hodgkin Lymphoma", "shortest_name_length": 36}
{"curie": "MONDO:0005144", "names": ["familial amyotrophic lateral sclerosis", "hereditary amyotrophic lateral sclerosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial amyotrophic lateral sclerosis", "shortest_name_length": 38}
{"curie": "UMLS:C1333112", "names": ["Colorectal Dysplasia", "Large Intestinal Dysplasia", "Colorectal Intraepithelial Neoplasia", "Large Intestinal Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Intraepithelial Neoplasia", "shortest_name_length": 20}
{"curie": "UMLS:C3897070", "names": ["Gliomatosis Cerebri", "Childhood Gliomatosis Cerebri", "childhood gliomatosis cerebri"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Gliomatosis Cerebri", "shortest_name_length": 19}
{"curie": "UMLS:C1832034", "names": ["Subependymal Giant Cell Astrocytoma", "Childhood Subependymal Giant Cell Astrocytoma", "childhood subependymal giant cell astrocytoma", "subependymal giant cell astrocytoma, childhood", "astrocytoma, childhood subependymal giant cell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Subependymal Giant Cell Astrocytoma", "shortest_name_length": 35}
{"curie": "UMLS:C5555128", "names": ["Refractory Aggressive B-Cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Aggressive B-Cell Non-Hodgkin Lymphoma", "shortest_name_length": 49}
{"curie": "MONDO:0018224", "names": ["HVLL", "HV-Like LPD", "HV-Like Lymphoma", "hV-like lymphoma", "Hydroa vacciniforme-like lymphoma", "hydroa vacciniforme-like lymphoma", "Hydroa Vacciniforme-Like Lymphoma", "Hydroa-like cutaneous T-cell lymphoma", "hydroa-like cutaneous T-cell lymphoma", "Hydroa vacciniforme-like lymphoma (disorder)", "hydroa vacciniforme-like lymphoma (diagnosis)", "Hydroa vacciniforme-like cutaneous T-cell lymphoma", "hydroa vacciniforme-like cutaneous T-cell lymphoma", "Hydroa Vacciniforme-Like Cutaneous T-Cell Lymphoma", "angiocentric cutaneous T-cell lymphoma of childhood", "Angiocentric cutaneous T-cell lymphoma of childhood", "Hydroa Vacciniforme-Like Lymphoproliferative Disorder", "Hydroa vacciniforme-like lymphoproliferative disorder", "hydroa vacciniforme-like lymphoproliferative disorder", "Hydroa vacciniforme-like lymphoma (morphologic abnormality)", "Hydroa vacciniforme-like cutaneous T-cell lymphoma (disorder)", "Hydroa vacciniforme-like lymphoproliferative disorder (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hydroa vacciniforme-like lymphoma", "shortest_name_length": 4}
{"curie": "UMLS:C4683017", "names": ["Stage III Eyelid Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Eyelid Carcinoma AJCC v8", "shortest_name_length": 34}
{"curie": "MONDO:0012426", "names": ["IMD25", "CD3zeta deficiency", "IMMUNODEFICIENCY 25", "immunodeficiency 25", "immunodeficiency type 25", "Immunodeficiency due to Defect in CD3-Zeta", "immunodeficiency due to defect in CD3-zeta", "IMMUNODEFICIENCY DUE TO DEFECT IN CD3-ZETA", "CD247 severe combined immunodeficiency (disease)", "severe combined immunodeficiency (disease) caused by mutation in CD247"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 25", "shortest_name_length": 5}
{"curie": "UMLS:C5667328", "names": ["Diffuse Midline Glioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse Midline Glioma", "shortest_name_length": 22}
{"curie": "MONDO:0045048", "names": ["Toxemia of Pregnancy", "toxemia of pregnancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "toxemia of pregnancy", "shortest_name_length": 20}
{"curie": "UMLS:C5239284", "names": ["Locally Advanced Anal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Anal Carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0011091", "names": ["CMT2D", "Cmt2d", "CMT 2D", "Charcot-Marie-Tooth disease Type 2D", "Charcot-Marie-Tooth disease type 2D", "Charcot-Marie-Tooth Disease Type 2D", "Charcot Marie Tooth disease type 2D", "Charcot-Marie-Tooth disease, Type 2D", "Charcot-Marie-Tooth disease, type 2D", "Charcot-Marie-Tooth neuropathy type 2D", "Charcot-Marie-Tooth neuropathy, type 2D", "GARS Charcot-Marie-Tooth disease type 2", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2D", "Charcot-Marie-Tooth Neuropathy, Type 2d", "Charcot-Marie-Tooth disease, axonal, Type 2D", "Charcot-Marie-Tooth disease neuronal type 2D", "Charcot-Marie-Tooth disease, axonal, type 2D", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2D", "CHARCOT-MARIE-TOOTH DISEASE, NEURONAL, TYPE 2D", "Charcot-Marie-Tooth disease, neuronal, type 2D", "Charcot-Marie-Tooth disease, neuronal, Type 2D", "Charcot-Marie-Tooth disease Type 2D (diagnosis)", "autosomal dominant Charcot-Marie-Tooth disease type 2D", "Autosomal dominant Charcot-Marie-Tooth disease type 2D", "Charcot-Marie-Tooth disease type 2 caused by mutation in GARS", "Autosomal dominant Charcot-Marie-Tooth disease type 2D (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 2D", "shortest_name_length": 5}
{"curie": "UMLS:C0334432", "names": ["Achromic nevus", "nevus achromic", "achromic nevus", "achromic naevus", "Achromic naevus", "Hypochromic nevus", "Nonpigmented nevus", "Nonpigmented Nevus", "Hypochromic naevus", "Nevus depigmentosus", "Nonpigmented naevus", "Non-pigmented nevus", "nevus depigmentosus", "non-pigmented nevus", "Non-pigmented naevus", "naevus depigmentosus", "Naevus depigmentosus", "Achromic nevus (disorder)", "Nonpigmented nevus (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Achromic nevus", "shortest_name_length": 14}
{"curie": "MONDO:0006066", "names": ["Prostate Acinar Adenocarcinoma, Foamy Gland Variant", "acinar prostate adenocarcinoma, foamy gland variant", "Acinar Prostate Adenocarcinoma, Foamy Gland Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acinar prostate adenocarcinoma, foamy gland variant", "shortest_name_length": 51}
{"curie": "MONDO:0008534", "names": ["GET", "HBT", "Hbt", "Hereditary benign telangiectasia", "telangiectasia, hereditary benign", "TELANGIECTASIA, HEREDITARY BENIGN", "Telangiectasia, Hereditary Benign", "generalized essential telangiectasia", "Generalized essential telangiectasia", "Generalised essential telangiectasia", "TELANGIECTASIA, GENERALIZED ESSENTIAL", "Telangiectasia, Generalized Essential", "telangiectasia, generalized essential", "Hereditary benign telangiectasia (disorder)", "Generalized essential telangiectasia (disorder)", "Generalized essential telangiectasia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "generalized essential telangiectasia", "shortest_name_length": 3}
{"curie": "UMLS:C0016549", "names": ["giant cell reaction", "Giant cell reaction", "reaction foreign body", "foreign body reaction", "Foreign body reaction", "Foreign Body Reaction", "Foreign-Body Reaction", "granuloma foreign body", "Foreign Body Granuloma", "foreign body; reaction", "Reaction, Foreign-Body", "foreign body granuloma", "Foreign-Body Granuloma", "Reaction, foreign body", "Foreign body granuloma", "reaction; foreign body", "foreign body; granuloma", "Foreign body granulomas", "Granuloma, Foreign-Body", "Granuloma, Foreign Body", "granuloma; foreign body", "body foreign granulomas", "Foreign-Body Granulomas", "Granulomas, Foreign-Body", "Foreign body giant cell reaction", "foreign body giant cell reaction", "Foreign body giant cell granuloma", "Foreign body giant cell granuloma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Foreign-Body Reaction", "shortest_name_length": 19}
{"curie": "MONDO:0006875", "names": ["hypertension ocular", "Hypertension ocular", "Ocular hypertension", "HYPERTENSION OCULAR", "ocular hypertension", "Ocular Hypertension", "ocular; hypertension", "Hypertension, Ocular", "hypertension; ocular", "Ocular Hypertensions", "Hypertensions, Ocular", "Pressure Behind Eyeballs", "OH - Ocular hypertension", "OHT - Ocular hypertension", "Ocular hypertension (disorder)", "preglaucoma ocular hypertension", "preglaucoma ocular hypertension (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ocular hypertension", "shortest_name_length": 19}
{"curie": "MONDO:0100172", "names": ["mental retardation, autosomal dominant", "autosomal dominant intellectual disability", "intellectual disability, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant", "shortest_name_length": 38}
{"curie": "MONDO:0013231", "names": ["LCA14", "LEBER CONGENITAL AMAUROSIS 14", "Leber Congenital Amaurosis 14", "Leber congenital amaurosis 14", "retinitis pigmentosa, juvenile", "LRAT Leber congenital amaurosis", "Leber congenital amaurosis type 14", "retinal dystrophy, early-onset severe", "Retinitis Pigmentosa, Juvenile, Lrat-Related", "RETINITIS PIGMENTOSA, JUVENILE, LRAT-RELATED", "retinitis pigmentosa, juvenile, LRAT-related", "RETINAL DYSTROPHY, EARLY-ONSET SEVERE, LRAT-RELATED", "retinal dystrophy, early-onset Severe, LRAT-related", "Retinal Dystrophy, Early-Onset Severe, Lrat-Related", "Leber congenital amaurosis caused by mutation in LRAT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leber congenital amaurosis 14", "shortest_name_length": 5}
{"curie": "UMLS:C5399824", "names": ["Odontogenic Carcinosarcoma", "Odontogenic carcinosarcoma", "Ameloblastic carcinosarcoma", "Ameloblastic Carcinosarcoma", "Malignant Odontogenic Mixed Tumor", "Odontogenic carcinosarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Odontogenic Carcinosarcoma", "shortest_name_length": 26}
{"curie": "UMLS:C3897733", "names": ["Recurrent Oropharyngeal Lymphoepithelioma", "Recurrent Oropharyngeal Undifferentiated Carcinoma", "Recurrent Oropharyngeal Throat Undifferentiated Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Oropharyngeal Undifferentiated Carcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0010537", "names": ["BFLS", "BORJ", "MRXSBFL", "BORJESON SYNDROME", "Borjeson Syndrome", "Borjeson syndrome", "Borjeson-FORSSMAN-Lehmann syndrome", "Borjeson-Forssman-Lehmann syndrome", "BORJESON-FORSSMAN-LEHMANN SYNDROME", "Borjeson-Forssman-Lehmann Syndrome", "Borjeson-Forssman-Lehmann syndrome (disorder)", "Borjeson-Forssman-Lehmann syndrome (diagnosis)", "Borjeson-Forssman-Lehmann syndrome (BFL, BFLS)", "Mental deficiency, epilepsy and endocrine disorders", "mental deficiency, epilepsy and endocrine disorders", "mental retardation, epilepsy, and endocrine disorder", "Mental Deficiency, Epilepsy, And Endocrine Disorders", "Mental Retardation, Epilepsy, and Endocrine Disorders", "mental retardation, epilepsy, and endocrine disorders", "MENTAL RETARDATION, EPILEPSY, AND ENDOCRINE DISORDERS", "Borjeson-Forssman-Lehmann syndrome, X-linked recessive", "mental deficiency-epilepsy-endocrine disorders syndrome", "intellectual disability, epilepsy, and endocrine disorder", "intellectual disability, epilepsy, and endocrine disorders", "intellectual deficiency-epilepsy-endocrine disorders syndrome", "intellectual disability-epilepsy-endocrine disorders syndrome", "Intellectual disability-epilepsy-endocrine disorders syndrome", "syndromic X-linked mental retardation Borjeson-Forssman-Lehmann type", "Mental Retardation, X-Linked, Syndromic, Borjeson-Forssman-Lehmann Type", "mental retardation, X-linked, syndromic, Borjeson-Forssman-Lehmann type", "MENTAL RETARDATION, X-LINKED, SYNDROMIC, BORJESON-FORSSMAN-LEHMANN TYPE", "syndromic X-linked intellectual disability Borjeson-Forssman-Lehmann type", "intellectual disability, X-linked, syndromic, Borjeson-Forssman-Lehmann type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borjeson-Forssman-Lehmann syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0016763", "names": ["spondylometaphyseal dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondylometaphyseal dysplasia", "shortest_name_length": 29}
{"curie": "MONDO:0020727", "names": ["COXPD22", "combined oxidative phosphorylation deficiency 22", "combined oxidative phosphorylation deficiency type 22"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation deficiency 22", "shortest_name_length": 7}
{"curie": "MONDO:0010765", "names": ["46,XY CGD", "46, XY CGD", "swyer syndrome", "Swyer Syndrome", "Swyer syndrome", "swyers syndrome", "Syndrome, Swyer", "46,XY SEX reversal", "46,XY sex reversal", "46,xy gonadal dysgenesis", "46,XY Gonadal Dysgenesis", "46,XY gonadal dysgenesis", "46 XY gonadal dysgenesis", "sex-reversing locus on X", "Gonadal dysgenesis, male", "Gonadal Dysgenesis, 46,XY", "46, XY Gonadal Dysgenesis", "Gonadal Dysgenesis, 46, XY", "XY Pure Gonadal Dysgenesis", "46, XY Gonadal Sex Reversal", "Pure gonadal dysgenesis 46,XY", "46,XY pure gonadal dysgenesis", "Sex Reversal, Gonadal, 46, XY", "Pure Gonadal Dysgenesis 46,XY", "pure gonadal dysgenesis 46,XY", "46, XY pure gonadal dysgenesis", "Pure Gonadal Dysgenesis, 46, XY", "46,XY Complete Gonadal Dysgenesis", "46,XY complete gonadal dysgenesis", "gonadal dysgenesis, XY female type", "46, XY complete gonadal dysgenesis", "sex-reversing locus on X, formerly", "Complete Gonadal Dysgenesis, 46, XY", "Pure gonadal dysgenesis 46,XY (disorder)", "testis-determining Factor, X-chromosomal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XY complete gonadal dysgenesis", "shortest_name_length": 9}
{"curie": "UMLS:C0392160", "names": ["ATROPHY APPLICATION SITE", "Atrophy application site", "Application site atrophy", "Application site atrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Application site atrophy", "shortest_name_length": 24}
{"curie": "EFO:0009783", "names": ["carotid atherosclerosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carotid atherosclerosis", "shortest_name_length": 23}
{"curie": "MONDO:0006997", "names": ["tibial neuropathy", "Tibial Neuropathy", "Tibial neuropathy", "Neuropathy, Tibial", "Tibial Neuropathies", "Tibial Nerve Disease", "Neuropathies, Tibial", "Tibial Nerve Diseases", "Nerve Disease, Tibial", "Nerve Diseases, Tibial", "Medial popliteal neuropathy", "Posterior tibial neuropathy", "Medial Popliteal Neuropathy", "Posterior Tibial Neuropathy", "Tibial neuropathy (disorder)", "Tibial Neuropathy, Posterior", "Neuropathy, Posterior Tibial", "Popliteal Neuropathy, Medial", "Neuropathy, Medial Popliteal", "Posterior Tibial Neuropathies", "Internal Popliteal Neuropathy", "Medial Popliteal Neuropathies", "tibial neuropathy (diagnosis)", "Tibial Neuropathies, Posterior", "Neuropathies, Posterior Tibial", "Neuropathies, Medial Popliteal", "Neuropathy, Internal Popliteal", "Popliteal Neuropathies, Medial", "Popliteal Neuropathy, Internal", "Posterior Tibial Nerve Diseases", "Internal Popliteal Neuropathies", "Popliteal Neuropathies, Internal", "Neuropathies, Internal Popliteal", "tibial neuropathy (disorder) [ambiguous]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tibial neuropathy", "shortest_name_length": 17}
{"curie": "MONDO:0016452", "names": ["Idiopathic hypersomnia without long sleep time", "idiopathic hypersomnia without long sleep time", "Idiopathic hypersomnia without long sleep time (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic hypersomnia without long sleep time", "shortest_name_length": 46}
{"curie": "UMLS:C1336255", "names": ["Stage III Peripheral T-cell Lymphoma", "Peripheral T-Cell Lymphoma Stage III", "Stage III Mature T- and NK-Cell Lymphoma", "Ann Arbor Stage III Mature T- and NK-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage III Mature T- and NK-Cell Lymphoma", "shortest_name_length": 36}
{"curie": "UMLS:C0280147", "names": ["Stage II Diffuse Small Cleaved Cell Lymphoma", "stage II adult diffuse small cleaved cell lymphoma", "Adult Diffuse Small Cleaved Cell Lymphoma Stage II", "Stage II Adult Diffuse Small Cleaved Cell Lymphoma", "adult diffuse small cleaved cell lymphoma, stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Adult Diffuse Small Cleaved Cell Lymphoma", "shortest_name_length": 44}
{"curie": "UMLS:C1336299", "names": ["Stage II Mixed Cellularity Hodgkin Lymphoma", "Mixed Cellularity Hodgkin's Disease Stage II", "Stage II Mixed Cellularity Hodgkin's Disease", "Mixed Cellularity Hodgkin's Lymphoma Stage II", "Stage II Mixed Cellularity Hodgkin's Lymphoma", "Stage II Mixed Cellularity Classical Hodgkin Lymphoma", "Ann Arbor Stage II Mixed Cellularity Classic Hodgkin Lymphoma", "Ann Arbor Stage II Mixed Cellularity Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage II Mixed Cellularity Classic Hodgkin Lymphoma", "shortest_name_length": 43}
{"curie": "MONDO:0004149", "names": ["gallbladder pleomorphic giant cell adenocarcinoma", "pleomorphic giant cell adenocarcinoma of the gallbladder", "Pleomorphic Giant cell adenocarcinoma of the gallbladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gallbladder pleomorphic giant cell adenocarcinoma", "shortest_name_length": 49}
{"curie": "MONDO:0004378", "names": ["Childhood Ependymoblastoma", "childhood ependymoblastoma", "Pediatric Cerebral Ependymoblastoma", "pediatric cerebral ependymoblastoma", "Childhood Cerebral Ependymoblastoma", "childhood cerebral ependymoblastoma", "Embryonal Tumor with Multilayered Rosettes, C19MC-Altered", "Childhood Embryonal Tumor with Multilayered Rosettes, C19MC-Altered", "childhood embryonal tumor with multilayered rosettes, C19MC-altered", "childhood cerebral embryonal tumor with Multilayered Rosettes, C19MC-altered", "Childhood Cerebral Embryonal Tumor with Multilayered Rosettes, C19MC-Altered"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pediatric cerebral ependymoblastoma", "shortest_name_length": 26}
{"curie": "UMLS:C1334272", "names": ["Invasive Breast Apocrine Carcinoma", "Invasive Apocrine Breast Carcinoma", "Invasive Apocrine Carcinoma of Breast", "Infiltrating Apocrine Breast Carcinoma", "Invasive Apocrine Carcinoma of the Breast", "Infiltrating Apocrine Carcinoma of Breast", "Infiltrating Apocrine Carcinoma of the Breast", "Invasive Breast Carcinoma with Apocrine Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Invasive Breast Apocrine Carcinoma", "shortest_name_length": 34}
{"curie": "UMLS:C0151738", "names": ["Large bowel perforation", "perforated large intestine", "Perforated large intestine", "Perforation large intestine", "LARGE INTESTINE PERFORATION", "PERFORATION LARGE INTESTINE", "Large intestine perforation", "Intestinal perforation large", "INTESTINAL PERFORATION LARGE", "intestine large perforations", "perforation of large intestine", "Perforation of large intestine", "Large intestinal perforation NOS", "Perforation of large intestine (disorder)", "perforation of large intestine (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Large intestine perforation", "shortest_name_length": 23}
{"curie": "MONDO:0010259", "names": ["RP24", "RP 24", "RETINITIS PIGMENTOSA 24", "retinitis pigmentosa 24", "retinitis pigmentosa type 24"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 24", "shortest_name_length": 4}
{"curie": "UMLS:C0278685", "names": ["stage I ovary cancer", "ovary cancer, stage I", "stage I ovarian cancer", "Stage I Ovarian Cancer", "Ovarian cancer stage I", "Ovarian Cancer Stage I", "ovarian cancer, stage I", "stage I ovarian carcinoma", "Stage I Ovarian Carcinoma", "ovarian carcinoma, stage I", "AJCC Stage I Ovarian Cancer", "FIGO Stage I Ovarian Cancer", "FIGO Stage I Cancer of Ovary", "Stage I Ovarian Cancer AJCC v7", "FIGO Stage I Ovarian Carcinoma", "Stage I Ovarian Cancer AJCC v6", "FIGO Stage I Carcinoma of Ovary", "FIGO Stage I Cancer of the Ovary", "stage I ovarian epithelial cancer", "Stage I Ovarian Epithelial Cancer", "Ovarian epithelial cancer stage I", "ovarian epithelial cancer, stage I", "FIGO Stage I Carcinoma of the Ovary", "Stage I Ovarian Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Ovarian Cancer AJCC v6 and v7", "shortest_name_length": 20}
{"curie": "MONDO:0015609", "names": ["Fasps", "FASPS", "advanced sleep phase syndrome", "Familial advanced sleep-phase syndrome", "familial advanced sleep-phase syndrome", "familial advanced sleep phase syndrome", "Familial advanced sleep phase syndrome", "advanced sleep phase syndrome, familial", "Advanced Sleep-Phase Syndrome, Familial", "Familial advanced sleep phase syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "advanced sleep phase syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0011315", "names": ["OSEBOLD SKELETAL DYSPLASIA/OSTEOLYSIS SYNDROME", "Osebold Skeletal Dysplasia Osteolysis Syndrome", "Osebold skeletal dysplasia/osteolysis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Osebold skeletal dysplasia/osteolysis syndrome", "shortest_name_length": 46}
{"curie": "UMLS:C1698634", "names": ["Soft tissue necrosis upper limb", "necrosis soft tissue upper limb", "necrosis of soft tissue of upper limb", "Upper Limb Soft Tissue Necrotic Lesion", "necrosis of soft tissue of upper limb (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Upper Limb Soft Tissue Necrotic Lesion", "shortest_name_length": 31}
{"curie": "MONDO:0017774", "names": ["LDL low", "ldl low", "Low LDL", "low ldl", "Decreased LDL", "decreasing ldl", "hypobetalipoproteinemia", "Hypobetalipoproteinemia", "Hypobetalipoproteinemias", "hypo-beta-lipoproteinemia", "Hypo-beta-lipoproteinemia", "Hypo beta Lipoproteinemia", "Hypo-beta-lipoproteinaemia", "Hypo beta Lipoproteinemias", "Decreased LDLc concentration", "Familial Hypobetalipoproteinemia", "Low density lipoprotein decreased", "Hypo-beta-lipoproteinemia (disorder)", "Decreased LDL cholesterol concentration", "Low density lipoprotein cholesterol low", "Low density lipoprotein cholesterol decreased", "Low density lipoprotein levels low (serum or plasma)", "Decreased circulating low-density lipoprotein levels"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypobetalipoproteinemia", "shortest_name_length": 7}
{"curie": "MONDO:0021172", "names": ["TS2", "ATS", "LQT8 type 2", "Atypical LQT8", "Timothy syndrome type 2", "atypical Timothy syndrome", "Timothy syndrome, atypical type", "Timothy syndrome type 2 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Timothy syndrome, atypical type", "shortest_name_length": 3}
{"curie": "MONDO:0008863", "names": ["STSL", "Sitosterolemia", "sitosterolemia", "phytosterolemia", "sitosterolaemia", "Sitosterolaemia", "Phytosterolemia", "PHYTOSTEROLEMIA", "Phytosterolaemia", "Sitosterolemia (disorder)", "Plant sterol storage disease", "plant sterol storage disease", "Pseudohomozygous familial hypercholesterolemia", "Pseudohomozygous familial hypercholesterolaemia", "macrothrombocytopenia/stomatocytosis, Mediterranean", "retention of dietary cholesterol and abnormal retention of non-cholesterol sterols in the body"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sitosterolemia", "shortest_name_length": 4}
{"curie": "UMLS:C3274502", "names": ["Opiate Withdrawal Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Opiate Withdrawal Syndrome", "shortest_name_length": 26}
{"curie": "UMLS:C4725808", "names": ["Refractory Malignant Pharyngeal Neoplasm", "Refractory Malignant Pharyngeal Throat Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Malignant Pharyngeal Neoplasm", "shortest_name_length": 40}
{"curie": "MONDO:0012253", "names": ["Multiple epiphyseal dysplasia with severe proximal femoral dysplasia", "multiple epiphyseal dysplasia with severe proximal femoral dysplasia", "Multiple epiphyseal dysplasia, with severe proximal femoral dysplasia", "multiple epiphyseal dysplasia, with severe proximal femoral dysplasia", "EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH SEVERE PROXIMAL FEMORAL DYSPLASIA", "Epiphyseal Dysplasia, Multiple, with Severe Proximal Femoral Dysplasia", "epiphyseal dysplasia, multiple, with severe proximal femoral dysplasia", "Multiple epiphyseal dysplasia with severe proximal femoral dysplasia (disorder)", "multiple epiphyseal dysplasia with severe proximal femoral dysplasia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple epiphyseal dysplasia, with severe proximal femoral dysplasia", "shortest_name_length": 68}
{"curie": "MONDO:0014116", "names": ["CDCBM2", "complex cortical dysplasia with other brain malformations 2", "cortical dysplasia, complex, with other brain malformations 2", "CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 2", "KIF5C complex cortical dysplasia with other brain malformations", "complex cortical dysplasia with other brain malformations type 2", "cortical dysplasia, Complex, with Other brain malformations type 2", "complex cortical dysplasia with other brain malformations caused by mutation in KIF5C"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complex cortical dysplasia with other brain malformations 2", "shortest_name_length": 6}
{"curie": "UMLS:C0265596", "names": ["clubhand", "clubhands", "Talipomanus", "talipomanus", "Talipomanus, NOS", "Congenital clubhand", "Congenital club hand", "Clubhand (congenital)", "Talipomanus (disorder)", "talipomanus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Talipomanus", "shortest_name_length": 8}
{"curie": "MONDO:0003861", "names": ["vulvar eccrine adenocarcinoma", "Vulvar Eccrine Adenocarcinoma", "eccrine adenocarcinoma of vulva", "mammalian vulva eccrine carcinoma", "eccrine carcinoma of mammalian vulva", "eccrine adenocarcinoma of vulva (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar eccrine adenocarcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0017479", "names": ["amelia of upper limb, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amelia of upper limb, bilateral", "shortest_name_length": 31}
{"curie": "UMLS:C0280187", "names": ["Recurrent Diffuse Mixed Cell Lymphoma", "Relapsed Adult Diffuse Mixed Cell Lymphoma", "relapsed adult diffuse mixed cell lymphoma", "recurrent adult diffuse mixed cell lymphoma", "Recurrent Adult Diffuse Mixed Cell Lymphoma", "adult diffuse mixed cell lymphoma, relapsed", "adult diffuse mixed cell lymphoma, recurrent", "diffuse mixed cell lymphoma, adult, recurrent", "diffuse mixed cell lymphoma, recurrent, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Adult Diffuse Mixed Cell Lymphoma", "shortest_name_length": 37}
{"curie": "MONDO:0016587", "names": ["ARVD", "ARVC", "ARVD-C", "arrhythmogenic RVD", "Arrhythmogenic RVD", "ARVC cardiomyopathy", "Boxer cardiomyopathy", "Right Ventricular Dysplasia", "right ventricular dysplasia", "Arrythmogenic right ventricular dysplasia", "Arrhythmogenic right ventricular dysplasia", "arrhythmogenic right ventricular dysplasia", "Arrhythmogenic Right Ventricular Dysplasia", "Right Ventricular Dysplasia, Arrhythmogenic", "Ventricular Dysplasia, Right, Arrhythmogenic", "Arrhythmogenic right ventricular cardiomyopathy", "Arrhythmogenic Right Ventricular Cardiomyopathy", "arrhythmogenic right ventricular cardiomyopathy", "Arrhythmogenic right ventricular dysplasia (disorder)", "arrhythmogenic right ventricular dysplasia (diagnosis)", "Arrhythmogenic Right Ventricular Dysplasia-Cardiomyopathy", "arrhythmogenic right ventricular dysplasia/cardiomyopathy", "Arrhythmogenic Right Ventricular Cardiomyopathy-Dysplasia", "Arrhythmogenic Right Ventricular Cardiomyopathy Dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arrhythmogenic right ventricular cardiomyopathy", "shortest_name_length": 4}
{"curie": "MONDO:0035838", "names": ["idiopathic multicentric Castleman disease", "HHV-8-negative multicentric Castleman disease", "Human herpesvirus-8-negative multicentric Castleman disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic multicentric Castleman disease", "shortest_name_length": 41}
{"curie": "MONDO:0012893", "names": ["OS5", "OA hip", "hip oa", "oa hip", "OA hips", "Coxarthrosis", "Coxarthroses", "coxarthrosis", "Hip arthrosis", "osteoarthritis-5", "DJD of hip joint", "Hip Osteoarthritis", "Hip osteoarthritis", "osteoarthritis hip", "Osteoarthritis;hip", "hip osteoarthritis", "Osteoarthritis, Hip", "Coxae malum senilis", "hips osteoarthritis", "Hips osteoarthritis", "GDF5 osteoarthritis", "osteoarthritis hips", "Osteoarthritis of hip", "of hip osteoarthritis", "Osteoarthritis Of Hip", "osteoarthritis of hip", "osteoarthrosis of hip", "Osteoarthrosis of hip", "OSTEOARTHRITIS OF HIP", "Osteoarthritis Of Hips", "Coxarthrosis, unspecified", "Osteoarthritis of the Hip", "osteoarthritis of the hip", "OA - Osteoarthritis of hip", "degenerative hip joint disease", "degenerative disease hip joint", "Coxarthrosis [arthrosis of hip]", "osteoarthritis susceptibility 5", "OSTEOARTHRITIS SUSCEPTIBILITY 5", "Osteoarthritis of hip (disorder)", "osteoarthritis of hip (diagnosis)", "Degenerative joint disease of hip", "osteoarthrosis of hip (diagnosis)", "Osteoarthritis of hip, unspecified", "osteoarthritis susceptibility type 5", "osteoarthritis caused by mutation in GDF5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteoarthritis susceptibility 5", "shortest_name_length": 3}
{"curie": "MONDO:0014233", "names": ["PARK20", "Parkinson's disease 20", "SYNJ1 Parkinson disease", "early-onset Parkinson disease 20", "Parkinson disease 20, early-onset", "PARKINSON DISEASE 20, EARLY-ONSET", "early-onset Parkinson's disease 20", "early-onset Parkinson disease type 20", "Parkinson disease caused by mutation in SYNJ1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early-onset Parkinson disease 20", "shortest_name_length": 6}
{"curie": "UMLS:C0026725", "names": ["mucous polyp cervix", "cervix mucous polyps", "CERVICAL POLYP MUCOUS", "Mucus polyp of cervix", "cervix; polyp, mucous", "polyp; cervix, mucous", "Mucous Polyp of Cervix", "cervical mucous polyps", "mucous polyp of cervix", "Mucous polyp of cervix", "Mucous polyp of cervix (disorder)", "mucous polyp of cervix (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mucous polyp of cervix", "shortest_name_length": 19}
{"curie": "MONDO:0014771", "names": ["JBTS26", "JOUBERT SYNDROME 26", "Joubert syndrome 26", "Joubert syndrome type 26", "KIAA0556 Joubert syndrome", "Joubert syndrome caused by mutation in KIAA0556"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome 26", "shortest_name_length": 6}
{"curie": "MONDO:0010449", "names": ["AUTSX5", "susceptibility to X-linked autism 5", "AUTISM, SUSCEPTIBILITY TO, X-LINKED 5", "autism, susceptibility to, X-linked 5", "autism, susceptibility to, X-linked type 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autism, susceptibility to, X-linked 5", "shortest_name_length": 6}
{"curie": "UMLS:C1334442", "names": ["Lung Carcinoma Metastatic to the Liver", "Lung Carcinoma Metastatic in the Liver"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Carcinoma Metastatic in the Liver", "shortest_name_length": 38}
{"curie": "UMLS:C0855155", "names": ["Primary Mediastinal Large B-Cell Lymphoma Stage I", "Primary mediastinal large B-cell lymphoma stage I", "Stage I Primary Mediastinal Large B-Cell Lymphoma", "Stage I Mediastinal (Thymic) Large B-Cell Lymphoma", "Ann Arbor Stage I Primary Mediastinal (Thymic) Large B-Cell Lymphoma", "Large B-cell lymphoma subtype primary mediastinal (Thymic) large B-cell lymphoma stage I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary mediastinal large B-cell lymphoma stage I", "shortest_name_length": 49}
{"curie": "MONDO:0002219", "names": ["paraurethral gland tumor", "Tumor of paraurethral gland", "paraurethral gland neoplasm", "tumor of paraurethral gland", "Tumour of paraurethral gland", "neoplasm of paraurethral gland", "neoplasm of paraurethral glands", "Neoplasm of paraurethral glands", "tumor of the Paraurethral gland", "tumor of the paraurethral gland", "paraurethral gland neoplasm (disease)", "Neoplasm of paraurethral glands (disorder)", "neoplasm of paraurethral gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paraurethral gland neoplasm", "shortest_name_length": 24}
{"curie": "UMLS:C5555710", "names": ["Recurrent Malignant Scrotal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Malignant Scrotal Neoplasm", "shortest_name_length": 36}
{"curie": "UMLS:C4525864", "names": ["Stage IIIB Rectal Neuroendocrine Tumor", "Stage IIIB Rectal Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Rectal Neuroendocrine Tumor AJCC v8", "shortest_name_length": 38}
{"curie": "UMLS:C1336881", "names": ["Ureteral Transitional Cell Carcinoma with Mixed Differentiation", "Transitional Cell Carcinoma of Ureter with Mixed Differentiation", "Infiltrating Ureter Urothelial Carcinoma with Mixed Differentiation", "Transitional Cell Carcinoma of the Ureter with Mixed Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infiltrating Ureter Urothelial Carcinoma with Mixed Differentiation", "shortest_name_length": 63}
{"curie": "UMLS:C2825773", "names": ["Malignant Leiomyoblastoma", "Malignant Epithelioid Cell Type Gastrointestinal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Epithelioid Cell Type Gastrointestinal Stromal Tumor", "shortest_name_length": 25}
{"curie": "UMLS:C4552690", "names": ["IA1", "Stage IA1 Cervical Cancer", "Stage IA1 Cervical Cancer AJCC v8", "Stage IA1 Cervical Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA1 Cervical Cancer AJCC v8", "shortest_name_length": 3}
{"curie": "UMLS:C0341558", "names": ["coli e enteritis", "e. coli enteritis", "E. coli enteritis NOS", "Enteric colibacillosis", "Escherichia gastroenteritis", "intestinal infection due to e. coli", "Intestinal infection due to E. coli", "Intestinal infection caused by E. coli", "infection; Escherichia coli, intestinal", "Escherichia coli; infection, intestinal", "intestinal infection due to Escherchia coli", "Intestinal infection due to escherichia coli", "Intestinal infection due to Escherichia coli", "infectious; enteritis, due to escherichia coli", "enteritis; infectious, due to escherichia coli", "Intestinal infection due to unspecified E. coli", "Intestinal infection caused by Escherichia coli", "intestinal infections bacterial escherchia coli", "Intestinal infection due to E. coli, unspecified", "Escherichia coli gastrointestinal tract infection", "Intestinal infection due to escherichia coli [E. coli]", "Intestinal infection due to Escherichia coli (E. coli)", "intestinal infection due to Escherchia coli (diagnosis)", "Intestinal infection caused by Escherichia coli (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal infection due to E. coli", "shortest_name_length": 16}
{"curie": "EFO:0009584", "names": ["AQP4-IgG-positive neuromyelitis optica"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AQP4-IgG-positive neuromyelitis optica", "shortest_name_length": 38}
{"curie": "MONDO:0037398", "names": ["pneumonia caused by pseudomonas aeruginosa infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pneumonia caused by pseudomonas aeruginosa infection", "shortest_name_length": 52}
{"curie": "UMLS:C4725008", "names": ["Refractory Sinonasal Squamous Cell Carcinoma", "Refractory Nasal Cavity and Paranasal Sinus Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Sinonasal Squamous Cell Carcinoma", "shortest_name_length": 44}
{"curie": "MONDO:0024476", "names": ["rectal epithelial tumor", "rectum epithelial neoplasm", "rectal epithelial neoplasm", "epithelial neoplasm of rectum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epithelial neoplasm of rectum", "shortest_name_length": 23}
{"curie": "UMLS:C0238305", "names": ["Sickle Cell Nephropathy", "Sickle cell nephropathy", "sickle cell nephropathy", "NEPHROPATHY, SICKLE CELL", "Sickle cell nephropathy (disorder)", "sickle cell nephropathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sickle cell nephropathy", "shortest_name_length": 23}
{"curie": "UMLS:C0151752", "names": ["LACTATION FEMALE", "FEMALE LACTATION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FEMALE LACTATION", "shortest_name_length": 16}
{"curie": "MONDO:0022011", "names": ["BHDS", "Bobble head doll syndrome", "Bobble-head doll syndrome", "bobble head doll syndrome", "bobble-head doll syndrome", "Bobble-head doll syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bobble-head doll syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0013232", "names": ["Mseleni joint disease", "MSELENI JOINT DISEASE", "Mseleni JOINT disease", "Brachydactylous dwarfs of Mseleni", "brachydactylous dwarfs of Mseleni", "Brachydactylous dwarfism Mseleni type", "brachydactylous dwarfism Mseleni type", "brachydactylous dwarfism, Mseleni type", "Brachydactylous dwarfism, Mseleni type", "Brachydactylous dwarfism Mseleni type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactylous dwarfism, Mseleni type", "shortest_name_length": 21}
{"curie": "UMLS:C4744473", "names": ["Broad Ligament Papillary Cystadenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Broad Ligament Papillary Cystadenoma", "shortest_name_length": 36}
{"curie": "MONDO:0015985", "names": ["bone dysplasia Azouz type", "bone dysplasia, Azouz type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bone dysplasia, Azouz type", "shortest_name_length": 25}
{"curie": "MONDO:0008118", "names": ["boder syndrome", "Boder syndrome", "odontoma-dysphagia syndrome", "ODONTOMA-DYSPHAGIA SYNDROME", "Odontoma-Dysphagia Syndrome", "odontoma dysphagia syndrome", "Odontoma dysphagia syndrome", "Odontoma dysphagia syndrome (disorder)", "odontomatosis-aortae esophagus stenosis syndrome", "Odontomatosis-aortae esophagus stenosis syndrome", "Odontomatosis (multiple odontomas) with dysphagia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "odontomatosis-aortae esophagus stenosis syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0030887", "names": ["CMD2G", "dilated cardiomyopathy 2G", "cardiomyopathy, dilated, 2G", "CARDIOMYOPATHY, DILATED, 2G"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiomyopathy, dilated, 2G", "shortest_name_length": 5}
{"curie": "MONDO:0030505", "names": ["PFIC8", "CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 8", "cholestasis, progressive familial intrahepatic, 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholestasis, progressive familial intrahepatic, 8", "shortest_name_length": 5}
{"curie": "MONDO:0045001", "names": ["cardiac ventricle disease", "cardiac ventricle disorder", "disease of cardiac ventricle", "disorder of cardiac ventricle", "Disorder of cardiac ventricle", "cardiac ventricle disease or disorder", "disease or disorder of cardiac ventricle", "Disorder of cardiac ventricle (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiac ventricle disorder", "shortest_name_length": 25}
{"curie": "MONDO:0017323", "names": ["Calciopenic Rickets", "Calciopenic rickets", "Hypocalcemic rickets", "hypocalcemic rickets", "Hypocalcaemic rickets", "Calcium Deficiency Rickets", "calcium deficiency rickets", "Hypocalcemic rickets (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypocalcemic rickets", "shortest_name_length": 19}
{"curie": "UMLS:C4521866", "names": ["Stage II Ampulla of Vater Cancer", "Stage II Ampulla of Vater Cancer AJCC v8", "Stage II Ampulla of Vater Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Ampulla of Vater Cancer AJCC v8", "shortest_name_length": 32}
{"curie": "MONDO:0006102", "names": ["Basaloid Carcinoma", "basaloid carcinoma", "Basaloid carcinoma", "carcinoma basaloid", "basaloid carcinoma (diagnosis)", "Basaloid carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "basaloid carcinoma", "shortest_name_length": 18}
{"curie": "MONDO:0007471", "names": ["DHD", "DHRD", "MLVT", "Dominant drusen", "familial drusen", "dominant drusen", "Familial drusen", "MALATTIA LEVENTINESE", "Malattia leventinese", "Malattia Leventinese", "dominant radial drusen", "Dominant radial drusen", "Dominant drusen (disorder)", "Doyne's honeycomb choroiditis", "DOYNE HONEYCOMB RETINAL DYSTROPHY", "Doyne honeycomb retinal dystrophy", "DRUSEN, RADIAL, AUTOSOMAL DOMINANT", "drusen, radial, autosomal dominant", "Drusen, Radial, Autosomal Dominant", "DOYNE HONEYCOMB DEGENERATION OF RETINA", "Doyne honeycomb degeneration of retina", "Hereditary dominant drusen retinal dystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Doyne honeycomb retinal dystrophy", "shortest_name_length": 3}
{"curie": "MONDO:0017345", "names": ["EBV-associated mesenchymal tumor", "Epstein-Barr virus-associated mesenchymal tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epstein-Barr virus-associated mesenchymal tumor", "shortest_name_length": 32}
{"curie": "MONDO:0014651", "names": ["AFDCIN", "POLR1A acrofacial dysostosis", "acrofacial dysostosis Cincinnati type", "ACROFACIAL DYSOSTOSIS, CINCINNATI TYPE", "acrofacial dysostosis, Cincinnati type", "acrofacial dysostosis caused by mutation in POLR1A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acrofacial dysostosis Cincinnati type", "shortest_name_length": 6}
{"curie": "MONDO:0010275", "names": ["Lkmcd", "LKMCD", "H-SMD", "SEMDHL", "leukoencephalopathy-SEMD syndrome", "SEMD X-linked with mental deterioration", "SEMD, X-LINKED, WITH MENTAL DETERIORATION", "SEMD, X-linked, with mental deterioration", "spondyloepimetaphyseal dysplasia, Bieganski type", "Skeletal dysplasia coarse facies mental retardation", "LEUKOENCEPHALOPATHY WITH METAPHYSEAL CHONDRODYSPLASIA", "Leukoencephalopathy With Metaphyseal Chondrodysplasia", "leukoencephalopathy with metaphyseal chondrodysplasia", "hypomyelination-spondyloepimetaphyseal dysplasia syndrome", "leukoencephalopathy-metaphyseal chondrodysplasia syndrome", "[OBSOLETE] Leukoencephalopathy With Metaphyseal Chondrodysplasia", "spondyloepimetaphyseal dysplasia X-linked with mental deterioration", "Spondyloepimetaphyseal dysplasia X-linked with mental deterioration", "spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration", "SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION", "Spondyloepimetaphyseal Dysplasia, X-Linked, with Mental Deterioration", "SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH HYPOMYELINATING LEUKODYSTROPHY", "spondyloepimetaphyseal dysplasia, X-linked, with hypomyelinating leukodystrophy, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepimetaphyseal dysplasia, Bieganski type", "shortest_name_length": 5}
{"curie": "UMLS:C0270246", "names": ["Meconium Plug", "Meconium plug", "meconium plug", "plug; meconium", "meconium; plug", "meconium obstruction", "Meconium obstruction", "obstruction; meconium", "meconium; obstruction", "meconium plug syndrome", "Meconium Plug Syndrome", "Meconium plug syndrome", "meconium; plug syndrome", "plug syndrome; meconium", "syndrome; meconium plug", "meconium plug; syndrome", "Meconium plug (disorder)", "meconium plug; obstruction", "obstruction; meconium plug", "Functional Immaturity of Colon", "meconium obstruction (diagnosis)", "meconium plug syndrome (diagnosis)", "Meconium obstruction in fetus or newborn", "obstruction; bowel, newborn, due to meconium (plug)", "bowel; obstruction, newborn, due to meconium (plug)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meconium plug syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0017763", "names": ["disorder of iron metabolism and transport"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of iron metabolism and transport", "shortest_name_length": 41}
{"curie": "UMLS:C1697884", "names": ["Esophageal necrosis", "esophageal necrosis", "Oesophageal necrosis", "Esophageal Necrotic Lesion", "esophageal necrosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Necrotic Lesion", "shortest_name_length": 19}
{"curie": "MONDO:0032822", "names": ["DEE80", "EIEE80", "GPIBD20", "early infantile epileptic encephalopathy 80", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 80", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 80", "developmental and epileptic encephalopathy 80", "epileptic encephalopathy, early infantile, 80", "developmental and epileptic encephalopathy, 80", "Glycosylphosphatidylinositol Biosynthesis Defect 20", "glycosylphosphatidylinositol biosynthesis defect 20", "GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 20"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 80", "shortest_name_length": 5}
{"curie": "UMLS:C1710174", "names": ["Lung Squamous Cell Carcinoma, Clear Cell Variant", "Squamous Cell Lung Carcinoma, Clear Cell Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Squamous Cell Carcinoma, Clear Cell Variant", "shortest_name_length": 48}
{"curie": "UMLS:C1334250", "names": ["Non-Comedo DCIS of Breast", "Non-Comedo DCIS of the Breast", "Non-Comedo Breast Ductal Carcinoma in situ", "Breast Intraductal Non-Comedo Adenocarcinoma", "Intraductal Non-Comedo Breast Adenocarcinoma", "Non-Comedo Ductal Carcinoma in situ of Breast", "Non-Invasive Non-Comedo Ductal Breast Carcinoma", "Breast Ductal Carcinoma In Situ, Non-Comedo Type", "Non-Comedo Ductal Carcinoma in situ of the Breast", "Non-Invasive Non-Comedo Ductal Carcinoma of Breast", "Non-Infiltrating Non-Comedo Ductal Breast Carcinoma", "Non-Infiltrating Non-Comedo Ductal Carcinoma of Breast", "Non-Invasive Non-Comedo Ductal Carcinoma of the Breast", "Non-Infiltrating Non-Comedo Ductal Carcinoma of the Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Ductal Carcinoma In Situ, Non-Comedo Type", "shortest_name_length": 25}
{"curie": "UMLS:C1557983", "names": ["fallopian tube perforation", "Fallopian tube perforation", "Fallopian Tube Perforation", "fallopian tube perforation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fallopian tube perforation", "shortest_name_length": 26}
{"curie": "UMLS:C4521618", "names": ["Stage IIB Bone Cancer", "Stage IIB Bone Cancer AJCC v8", "Stage IIB Appendicular Skeleton, Trunk, Skull, and Facial Bones Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Bone Cancer AJCC v8", "shortest_name_length": 21}
{"curie": "MONDO:0019584", "names": ["localized lichen myxedematosus with monoclonal gammopathy or systemic symptoms"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "localized lichen myxedematosus with monoclonal gammopathy or systemic symptoms", "shortest_name_length": 78}
{"curie": "MONDO:0019092", "names": ["infant apnea", "apnea infant", "INFANT APNEA", "apnea infants", "infantile apnea", "Infantile apnea", "Infantile apnoea", "Apnea of infancy", "apnea of infancy", "Apnoea of infancy", "Apnea in full-term infants", "Apnea of infancy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile apnea", "shortest_name_length": 12}
{"curie": "MONDO:0010983", "names": ["DYT9", "DYSTONIA 9", "Dystonia 9", "dystonia 9", "dystonia type 9", "episodic choreoathetosis/spasticity", "Episodic choreoathetosis/spasticity", "Choreoathetosis-Spasticity, Episodic", "CHOREOATHETOSIS/SPASTICITY, EPISODIC", "choreoathetosis/spasticity, episodic", "Choreoathetosis, Paroxysmal, with Episodic Ataxia", "Cse choreoathetosis, paroxysmal, with episodic ataxia", "CSE CHOREOATHETOSIS, PAROXYSMAL, WITH EPISODIC ATAXIA", "CHOREOATHETOSIS, KINESIGENIC, WITH EPISODIC ATAXIA AND SPASTICITY", "Choreoathetosis, Kinesigenic, with Episodic Ataxia And Spasticity", "choreoathetosis, kinesigenic, with episodic ataxia and spasticity", "Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity", "paroxysmal dystonic choreathetosis with episodic ataxia and spasticity", "Paroxysmal dystonic choreoathetosis with episodic ataxia and spasticity", "Paroxysmal dystonic choreoathetosis with episodic ataxia and spasticity (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dystonia 9", "shortest_name_length": 4}
{"curie": "MONDO:0021427", "names": ["lip scc", "Lip SCC", "SCC of Lip", "scc of Lip", "SCC of the Lip", "scc of the Lip", "Lip Squamous Cell Carcinoma", "lip squamous cell carcinoma", "Lip squamous cell carcinoma", "Squamous cell carcinoma of lip", "Squamous Cell Carcinoma of Lip", "squamous cell carcinoma of lip", "Squamous Cell Carcinoma of the Lip", "squamous cell carcinoma of the Lip", "Squamous cell carcinoma of the lip", "SCC - Squamous cell carcinoma of lip", "Squamous cell carcinoma of lip (disorder)", "squamous cell carcinoma of lip (diagnosis)", "lip neoplasm malignant carcinoma squamous cell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "squamous cell carcinoma of lip", "shortest_name_length": 7}
{"curie": "MONDO:0008281", "names": ["POLYPS, SCATTERED, DISCRETE INTESTINAL", "polyps, scattered, discrete intestinal", "polyposis, intestinal, scattered and discrete", "POLYPOSIS, INTESTINAL, SCATTERED AND DISCRETE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyposis, intestinal, scattered and discrete", "shortest_name_length": 38}
{"curie": "MONDO:0008022", "names": ["MUSCLE CRAMPS, FAMILIAL", "Muscle Cramps, Familial", "muscle cramps, familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscle cramps, familial", "shortest_name_length": 23}
{"curie": "MONDO:0800101", "names": ["LCA9", "SHILCA", "SHILCA Syndrome", "NMNAT1-related retinopathy", "Leber congenital amaurosis 9", "Leber congenital amaurosis type 9", "NMNAT1 Leber congenital amaurosis", "amaurosis congenita of Leber, type 9", "Leber congenital amaurosis caused by mutation in NMNAT1", "spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "NMNAT1-related retinopathy", "shortest_name_length": 4}
{"curie": "UMLS:C1334184", "names": ["Infratentorial Glioblastoma", "Infratentorial Glioblastoma Multiforme"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infratentorial Glioblastoma", "shortest_name_length": 27}
{"curie": "MONDO:0024615", "names": ["T-Cell Neoplasm", "T-cell neoplasm", "T-cell and NK-cell neoplasm", "T-Cell and NK-Cell Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-cell and NK-cell neoplasm", "shortest_name_length": 15}
{"curie": "MONDO:0018007", "names": ["Mosaic genome-wide paternal UPD", "androgenetic/biparental mosaicism", "mosaic genome-wide paternal uniparental disomy", "genome-wide paternal uniparental disomy mosaicism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mosaic genome-wide paternal uniparental disomy", "shortest_name_length": 31}
{"curie": "UMLS:C0151584", "names": ["INJECTION SITE CYST", "Injection site cyst", "CYST INJECTION SITE", "Cyst injection site", "Injection site cyst (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site cyst", "shortest_name_length": 19}
{"curie": "MONDO:0005657", "names": ["aspergillose", "ASPERGILLOSIS", "Aspergilloses", "aspergillosis", "aspergilloses", "Aspergillosis", "Aspergillosis NOS", "Aspergillosis, NOS", "Aspergillus Infection", "aspergillus infection", "Aspergillus infection", "infection; Aspergillus", "Aspergillus; infection", "Infection, Aspergillus", "Aspergillus Infections", "aspergillus infections", "Aspergillus infections", "Infections, Aspergillus", "Aspergillosis (disorder)", "Aspergillus infection NOS", "aspergillosis (diagnosis)", "Aspergillosis, unspecified", "Infection due to Aspergillus", "infection due to Aspergillus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aspergillosis", "shortest_name_length": 12}
{"curie": "MONDO:0017582", "names": ["PTCA", "Pituitary Cancer", "pituitary cancer", "Pituitary Cancers", "Metastatic PitNET", "Cancer, Pituitary", "Cancers, Pituitary", "cancer of pituitary", "Pituitary Carcinoma", "Pituitary carcinoma", "Cancer of Pituitary", "carcinoma pituitary", "pituitary carcinoma", "Pituitary Carcinomas", "Carcinoma, Pituitary", "Carcinomas, Pituitary", "pituitary gland cancer", "Pituitary Gland Cancer", "carcinoma of pituitary", "Carcinoma of Pituitary", "Pituitary gland--Cancer", "cancer of the pituitary", "Cancer of the Pituitary", "Pituitary carcinoma, NOS", "pituitary adenocarcinoma", "Cancer of Pituitary Gland", "cancer of pituitary gland", "Pituitary Gland Carcinoma", "pituitary gland carcinoma", "carcinoma of the pituitary", "Carcinoma of the Pituitary", "Pituitary gland cancer, NOS", "Carcinoma of Pituitary Gland", "carcinoma of pituitary gland", "Cancer of the Pituitary Gland", "cancer of the pituitary gland", "pituitary gland adenocarcinoma", "Pituitary Gland Adenocarcinoma", "Pituitary carcinoma (disorder)", "carcinoma of the pituitary gland", "carcinoma of the Pituitary gland", "Carcinoma of the Pituitary Gland", "pituitary adenocarcinoma (disease)", "Metastatic Pituitary Gland Carcinoma", "carcinoma of pituitary gland (diagnosis)", "Metastatic Pituitary Neuroendocrine Tumor", "Pituitary carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pituitary adenocarcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0044879", "names": ["mucinous cystic neoplasm", "Pancreatic Mucinous Cystic Neoplasm", "Pancreatic mucinous cystic neoplasm", "Pancreatic mucinous-cystic neoplasm", "pancreatic mucinous-cystic neoplasm", "Pancreatic Mucinous-Cystic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic mucinous-cystic neoplasm", "shortest_name_length": 24}
{"curie": "MONDO:0009647", "names": ["MORQUIO SYNDROME C", "Morquio syndrome C", "Morquio Syndrome C", "Morquio syndrome type C", "Nonkeratan-sulfate-excreting Morquio syndrome", "Morquio Syndrome, Nonkeratosulfate-Excreting Type", "MORQUIO SYNDROME, NONKERATOSULFATE-EXCRETING TYPE", "Morquio syndrome, Nonkeratosulfate-Excreting type", "Morquio syndrome, nonkeratan-sulfate-excreting type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Morquio syndrome C", "shortest_name_length": 18}
{"curie": "UMLS:C4331231", "names": ["Recurrent Primary Malignancy", "Recurrent Primary Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Primary Malignant Neoplasm", "shortest_name_length": 28}
{"curie": "MONDO:0015723", "names": ["12p trisomy", "Trisomy 12p", "trisomy 12p", "12p+ syndrome", "Duplication 12p", "12p duplication", "trisomy type 12p", "dup(12p) syndrome", "partial trisomy 12p", "chromosome 12p trisomy", "duplication 12p syndrome", "12p duplication syndrome", "chromosome 12p duplication", "Chromosome 12, 12p trisomy", "chromosome 12p duplication syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trisomy 12p", "shortest_name_length": 11}
{"curie": "MONDO:0016577", "names": ["BASM syndrome", "biliary atresia with splenic malformation syndrome", "Biliary atresia with splenic malformation syndrome", "Biliary atresia with splenic malformation syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "biliary atresia with splenic malformation syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0013875", "names": ["MGCA6", "MEGDEL", "MEGDHEL", "SERAC1 defect", "MEGDEL syndrome", "3-MGCA-4 (formerly)", "3-MGCA type IV (formerly)", "3-methylglutaconic aciduria type 6", "SERAC1 3-methylglutaconic aciduria", "3-Methylglutaconic aciduria, type 6", "3-methylglutaconic aciduria type VI", "3-METHYLGLUTACONIC ACIDURIA, TYPE VI", "3-methylglutaconic aciduria caused by mutation in SERAC1", "3-methylglutaconic aciduria with deafness-encephalopathy-Leigh-like syndrome", "3-methylglutaconic aciduria with hearing loss-encephalopathy-Leigh-like syndrome", "3-METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME", "3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome", "3-@METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME", "3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome", "3-Methylglutaconic aciduria with dystonia-deafness, hepatopathy, encephalopathy, and Leigh-like syndrome", "3-METHYLGLUTACONIC ACIDURIA WITH DYSTONIA-DEAFNESS, HEPATOPATHY, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME", "3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0009631", "names": ["MCOP", "Mcop", "MCOP1", "isolated microphthalmia 1", "Microphthalmia, Isolated 1", "MICROPHTHALMIA, ISOLATED 1", "microphthalmia, isolated 1", "isolated microphthalmia type 1", "ANOPHTHALMIA, CLINICAL, ISOLATED", "anophthalmia, clinical, isolated", "Microphthalmos, Autosomal Recessive", "microphthalmos, autosomal recessive", "MICROPHTHALMOS, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated microphthalmia 1", "shortest_name_length": 4}
{"curie": "MONDO:0010027", "names": ["NSD", "ISSD", "Nana storage disease", "French Type Sialuria", "NANA STORAGE DISEASE", "Sialuria, French type", "SIALURIA, FRENCH TYPE", "Infantile Form Sialuria", "Infantile Form Sialurias", "Sialuria, infantile type", "sialuria, infantile form", "SIALURIA, INFANTILE FORM", "Sialuria, Infantile Form", "Sialurias, Infantile Form", "Infantile sialic acid storage disease", "Infantile Sialic Acid Storage Disease", "INFANTILE SIALIC ACID STORAGE DISEASE", "infantile sialic acid storage disease", "Infantile Sialic Acid Storage Disorder", "infantile sialic acid storage disorder", "INFANTILE SIALIC ACID STORAGE DISORDER", "N-acetylneuraminic acid storage disease", "sialic acid storage disorder, infantile", "N-Acetylneuraminic acid storage disease", "N-ACETYLNEURAMINIC ACID STORAGE DISEASE", "infantile free sialic acid storage disease", "Sialic Acid Storage Disease, Infantile Form", "infantile sialic acid storage disorder (ISSD)", "Infantile Sialic Acid Storage Disorder (ISSD)", "free sialic acid storage disease, infantile form", "Free sialic acid storage disease, infantile form", "Sialic acid storage disease, severe infantile type", "Sialic acid storage disease, severe infantile type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "free sialic acid storage disease, infantile form", "shortest_name_length": 3}
{"curie": "UMLS:C0746014", "names": ["Lumbar Spine Kyphosis", "LUMBAR SPINE KYPHOSIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lumbar Spine Kyphosis", "shortest_name_length": 21}
{"curie": "UMLS:C1096341", "names": ["Injection site pustule"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site pustule", "shortest_name_length": 22}
{"curie": "MONDO:0018364", "names": ["Ovarian carcinoma", "Carcinoma of ovary", "ovarian stromal cancer", "Ovarian stromal cancer", "cancer, ovarian stromal", "stromal cancer, ovarian", "ovarian epithelial cancer", "epithelial cancer of ovary", "malignant ovarian epithelial tumor", "Malignant Ovarian Epithelial Tumor", "ovarian malignant epithelial tumor", "ovarian epithelial tumor, malignant", "Malignant epithelial tumor of ovary", "malignant epithelial tumor of ovary", "[OBSOLETE] Ovarian epithelial cancer", "Malignant epithelial tumour of ovary", "Malignant epithelial tumor of ovary (disorder)", "malignant ovarian surface epithelial-stromal tumor", "Malignant Ovarian Surface Epithelial-Stromal Tumor", "malignant ovarian surface epithelial-stromal neoplasm", "Malignant Ovarian Surface Epithelial-Stromal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant epithelial tumor of ovary", "shortest_name_length": 17}
{"curie": "UMLS:C5556454", "names": ["Uterine Corpus Myxoid STUMP", "Uterine Corpus Myxoid Smooth Muscle Tumor of Uncertain Malignant Potential"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Corpus Myxoid Smooth Muscle Tumor of Uncertain Malignant Potential", "shortest_name_length": 27}
{"curie": "MONDO:0000337", "names": ["roseola", "ROSEOLA", "Roseola", "pseudorubella", "Sixth Disease", "sixth disease", "disease sixth", "Pseudorubella", "SIXTH DISEASE", "Sixth disease", "Disease, Sixth", "Three day fever", "three day fever", "Roseola Infantum", "Exanthem Subitum", "three-day; fever", "Roseola infantum", "roseola infantum", "exanthem subitum", "fever; three-day", "roseola Infantum", "ROSEOLA INFANTUM", "infantum roseola", "Exanthem subitum", "EXANTHEM SUBITUM", "Exanthema subitum", "infantum; roseola", "exanthema subitum", "subitum exanthema", "roseola; infantum", "Exanthema Subitum", "subitum; exanthem", "exanthema; subitum", "Sixth disease, unspecified", "roseola infantum (diagnosis)", "Exanthema subitum (disorder)", "Roseola infantum, unspecified", "Exanthema subitum, unspecified", "Exanthema subitum [sixth disease]", "Roseola rash of secondary syphilis", "disease (or disorder); sixth disease", "Exanthema subitum [sixth disease], unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exanthema subitum", "shortest_name_length": 7}
{"curie": "MONDO:0033169", "names": ["curariform drugs toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "curariform drugs toxicity", "shortest_name_length": 25}
{"curie": "MONDO:0013892", "names": ["C3G3", "CFHR5 deficiency", "CFHR5 NEPHROPATHY", "C3 GLOMERULOPATHY 3", "C3 Glomerulonephritis", "C3 glomerulonephritis", "nephropathy due to CFHR5 deficiency", "complement-mediated membranoproliferative glomerulonephritis", "Complement-Mediated Membranoproliferative Glomerulonephritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "C3 glomerulonephritis", "shortest_name_length": 4}
{"curie": "MONDO:0007095", "names": ["AMELOONYCHOHYPOHIDROTIC SYNDROME", "ameloonychohypohidrotic syndrome", "Ameloonychohypohidrotic syndrome", "amelo-onycho-hypohidrotic syndrome", "Amelo-onycho-hypohidrotic syndrome", "Ameloonychohypohidrotic syndrome (disorder)", "Ameloonychohypohidrotic ectodermal dysplasia", "hypocalcified-hypoplastic enamel, onycholysis with subungual hyperkeratosis, and hypohidrosis", "Hypocalcified-hypoplastic enamel, onycholysis with subungual hyperkeratosis, and hypohidrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ameloonychohypohidrotic syndrome", "shortest_name_length": 32}
{"curie": "MONDO:0013957", "names": ["IMD32A", "immunodeficiency 32A", "IMMUNODEFICIENCY 32A", "immunodeficiency type 32A", "MSMD due to partial IRF8 deficiency", "IRF8 DEFICIENCY, AUTOSOMAL DOMINANT", "IRF8 deficiency, autosomal dominant", "immunodeficiency 32A, Mycobacteriosis, autosomal dominant", "IMMUNODEFICIENCY 32A, MYCOBACTERIOSIS, AUTOSOMAL DOMINANT", "immunodeficiency 32A, mycobacteriosis, autosomal dominant", "MSMD due to partial interferon regulatory factor 8 deficiency", "CD11C-POSITIVE/CD1C-POSITIVE DENDRITIC CELL DEFICIENCY, AUTOSOMAL DOMINANT", "CD11c-positive/CD1c-positive Dendritic cell deficiency, autosomal dominant", "Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency", "IRF8 autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency", "Mendelian susceptibility to mycobacterial diseases due to partial interferon regulatory factor 8 deficiency", "autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency caused by mutation in IRF8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency", "shortest_name_length": 6}
{"curie": "MONDO:0011780", "names": ["SLI3", "specific language impairment 3", "SPECIFIC LANGUAGE IMPAIRMENT 3", "specific language impairment QTL, 3", "SPECIFIC LANGUAGE IMPAIRMENT QUANTITATIVE TRAIT LOCUS ON CHROMOSOME 13", "specific language impairment quantitative trait locus on chromosome 13"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "specific language impairment 3", "shortest_name_length": 4}
{"curie": "MONDO:0009406", "names": ["Cantú syndrome", "Cantu syndrome", "CANTU SYNDROME", "Cantu's syndrome", "Cantu's syndrome (disorder)", "Craniofaciocardioskeletal syndrome", "HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA", "Hypertrichotic osteochondrodysplasia", "hypertrichotic osteochondrodysplasia", "hypertrichotic osteochondrodysplasia Cantu type", "hypertrichotic osteochondrodysplasia, Cantu type", "hypertrichotic osteochondrodysplasia (Cantu syndrome)", "dwarfism-cerebral atrophy-keratosis follicularis syndrome", "Congenital hypertrichosis-coarse facial features spectrum", "Hypertrichosis-Osteochondrodysplasia-Cardiomegaly Syndrome", "Congenital hypertrichosis-acromegaloid facial features spectrum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrichotic osteochondrodysplasia Cantu type", "shortest_name_length": 14}
{"curie": "MONDO:0010595", "names": ["SCOS", "SPGFX1", "Germinal aplasia", "Azoospermia factor", "GERMINAL CELL APLASIA", "Del Castillo Syndrome", "Germinal cell absence", "Germinal Cell Aplasia", "Del Castillo syndrome", "DEL CASTILLO SYNDROME", "Sertoli-only-syndrome", "Germinal cell aplasia", "DEL CASTILLO syndrome", "Del Castillo's syndrome", "AZF - Azoospermia factor", "Germinal aplasia syndrome", "Sertoli Cell Only Syndrome", "Sertoli cell-only syndrome", "SERTOLI CELL-ONLY SYNDROME", "Sertoli Cell-Only Syndrome", "Sertoli-cell-only syndrome", "SPERMATOGENIC FAILURE, X-LINKED, 1", "Gene deletion in AZF region of Y chromosome", "Congenital absence of germinal epithelium of testes", "Congenital absence of germinal epithelium of testes (disorder)", "Congenital absence of germinal epithelium of testes (diagnosis)", "anomalies of genital organs absence of germinal epithelium of testes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sertoli cell-only syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0019668", "names": ["Pancreatic adenoma", "pancreatic adenoma", "adenoma of pancreas", "Adenoma of pancreas", "adenoma of the pancreas", "Adenoma of pancreas (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenoma of pancreas", "shortest_name_length": 18}
{"curie": "MONDO:0019436", "names": ["JPsA", "Psoriasis-related JIA", "psoriasis-related JIA", "Juvenile Oligoarthritis", "Oligoarthritis, Juvenile", "juvenile psoriatic arthritis", "Juvenile Psoriatic Arthritis", "Juvenile psoriatic arthritis", "Psoriatic Arthritis, Juvenile", "Arthritis, Juvenile Psoriatic", "Juvenile Enthesitis-Related Arthritis", "Enthesitis Related Arthritis, Juvenile", "Arthritis, Juvenile Enthesitis-Related", "Enthesitis-Related Arthritis, Juvenile", "Juvenile psoriatic arthritis (disorder)", "psoriasis-related juvenile idiopathic arthritis", "Psoriasis-related juvenile idiopathic arthritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "psoriasis-related juvenile idiopathic arthritis", "shortest_name_length": 4}
{"curie": "MONDO:0019075", "names": ["BSAS", "Bosley-Salih-Alorainy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bosley-Salih-Alorainy syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C4054369", "names": ["Parvovirus B19 Associated Nephrotic Syndrome", "Nephrotic Syndrome - Parvovirus B19 Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - Parvovirus B19 Associated", "shortest_name_length": 44}
{"curie": "MONDO:0005072", "names": ["NB", "Neuroblastoma", "neuroblastoma", "NEUROBLASTOMA", "neuroblastomas", "Neuroblastomas", "Neuroblastoma NOS", "NB - Neuroblastoma", "Neuroblastoma, NOS", "Neuroblastoma (NBL)", "Central neuroblastoma", "central neuroblastoma", "NEUROBLASTOMA, MALIGNANT", "neuroblastoma, malignant", "Neuroblastoma (disorder)", "neuroblastoma (diagnosis)", "Cancer of early nerve cells", "Neural Crest Tumor, Malignant", "neural Crest tumor, malignant", "neuroblastoma; unspecified site", "neuroblastoma (Schwannian Stroma-poor)", "Neuroblastoma (Schwannian Stroma-Poor)", "Neuroblastoma (Schwannian Stroma-poor)", "Neuroblastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuroblastoma", "shortest_name_length": 2}
{"curie": "MONDO:0013088", "names": ["FL1", "FOLLICULAR LYMPHOMA, SUSCEPTIBILITY TO, 1", "follicular lymphoma, susceptibility to, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "follicular lymphoma, susceptibility to, 1", "shortest_name_length": 3}
{"curie": "MONDO:0014459", "names": ["AOS5", "ADAMS-OLIVER SYNDROME 5", "Adams-Oliver syndrome 5", "NOTCH1 Adams-Oliver syndrome", "Notch1 Adams-Oliver syndrome", "Adams-Oliver syndrome type 5", "Adams-Oliver syndrome caused by mutation in Notch1", "Adams-Oliver syndrome caused by mutation in NOTCH1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adams-Oliver syndrome 5", "shortest_name_length": 4}
{"curie": "UMLS:C3897569", "names": ["Slipped Muscle", "Slipped extraocular muscle", "Slipped Extraocular Muscle"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Slipped extraocular muscle", "shortest_name_length": 14}
{"curie": "MONDO:0011810", "names": ["HGPPS", "Hgpps", "Horizontal gaze palsy with progressive scoliosis", "horizontal gaze palsy with progressive scoliosis", "Horizontal Gaze Palsy with Progressive Scoliosis", "gaze palsy, horizontal, with progressive scoliosis", "progressive external ophthalmoplegia and scoliosis", "Progressive external ophthalmoplegia and scoliosis", "OPHTHALMOPLEGIA, PROGRESSIVE EXTERNAL, AND SCOLIOSIS", "Ophthalmoplegia, Progressive External, and Scoliosis", "ophthalmoplegia, progressive external, and scoliosis", "HGPPS, Horizontal Gaze Palsy with Progressive Scoliosis", "Horizontal gaze palsy with progressive scoliosis (HGPPS)", "HGPPS - horizontal gaze palsy with progressive scoliosis", "Familial Horizontal Gaze Palsy with Progressive Scoliosis", "Horizontal gaze palsy with progressive scoliosis (disorder)", "gaze palsy, familial horizontal, with progressive scoliosis", "Familial Idiopathic Scoliosis Associated with Congenital Encephalopathy", "Familial infantile scoliosis associated with bilateral paralysis of conjugate gaze", "Familial Infantile Scoliosis Associated with Bilateral Paralysis of Conjugate Gaze"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "horizontal gaze palsy with progressive scoliosis", "shortest_name_length": 5}
{"curie": "UMLS:C0863185", "names": ["Ectopic chorionic gonadotropin secretion", "Ectopic Chorionic Gonadotropin Secretion", "Ectopic chorionic gonadotrophin secretion", "Ectopic Chorionic Gonadotropin Secretion Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ectopic Chorionic Gonadotropin Secretion Syndrome", "shortest_name_length": 40}
{"curie": "MONDO:0000971", "names": ["Chest Wall Lipoma", "chest wall lipoma", "Lipoma of Chest Wall", "Lipoma of chest wall", "lipoma of chest wall", "lipoma of the chest wall", "Lipoma of the Chest Wall", "Lipoma of chest wall (disorder)", "Lipoma of chest wall (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chest wall lipoma", "shortest_name_length": 17}
{"curie": "MONDO:0020959", "names": ["Filariasis ozzardi", "filariasis ozzardi", "Ozzardian filariasis", "ozzardian filariasis", "Filariasis, Ozzardian", "MANSONELLIASIS OZZARDI", "mansonella ozzardi infection", "Mansonella ozzardi infection", "Mansonella Ozzardi Infection", "Mansonella ozzardi; filariasis", "filariasis; Mansonella ozzardi", "Ozzardian filariasis (disorder)", "ozzardian filariasis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mansonella ozzardi infection", "shortest_name_length": 18}
{"curie": "UMLS:C1333636", "names": ["Foveolar Hyperplasia", "Foveolar hyperplasia", "Hyperplasia of gastric foveola", "Hyperplasia of gastric foveola (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Foveolar hyperplasia", "shortest_name_length": 20}
{"curie": "UMLS:C3640026", "names": ["Acquired Unilateral Cataract", "Cataract, Acquired, Unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired Unilateral Cataract", "shortest_name_length": 28}
{"curie": "UMLS:C4526973", "names": ["Stage IV Gastric and Omental GIST AJCC v8", "Stage IV Gastric and Omental Gastrointestinal Stromal Tumor AJCC v8", "Stage IV Gastric (Stomach) and Omental Gastrointestinal Stromal Tumor (GIST)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Gastric and Omental Gastrointestinal Stromal Tumor AJCC v8", "shortest_name_length": 41}
{"curie": "MONDO:0044321", "names": ["SHDRA", "STRUCTURAL HEART DEFECTS AND RENAL ANOMALIES SYNDROME", "structural heart defects and renal anomalies syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "structural heart defects and renal anomalies syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0018055", "names": ["Pediatric HCC", "pediatric HCC", "Childhood Hepatoma", "Pediatric Hepatoma", "pediatric hepatoma", "childhood hepatoma", "childhood-onset HCC", "Childhood-onset HCC", "hepatocellular cancer", "Hepatocellular Cancer", "childhood liver cell carcinoma", "Childhood Liver Cell Carcinoma", "pediatric liver cell carcinoma", "Pediatric Liver Cell Carcinoma", "Childhood Carcinoma of Liver Cell", "childhood carcinoma of liver cell", "Pediatric Carcinoma of Liver Cell", "pediatric carcinoma of liver cell", "Pediatric hepatocellular carcinoma", "childhood hepatocellular carcinoma", "pediatric hepatocellular carcinoma", "Pediatric Hepatocellular Carcinoma", "Childhood Hepatocellular Carcinoma", "hepatocellular carcinoma, childhood", "Paediatric hepatocellular carcinoma", "carcinoma, hepatocellular, childhood", "Pediatric carcinoma of the liver cell", "Childhood Carcinoma of the Liver Cell", "childhood carcinoma of the liver cell", "Pediatric Carcinoma of the Liver Cell", "Childhood-onset hepatocellular carcinoma", "childhood-onset hepatocellular carcinoma", "Pediatric HCC (hepatocellular carcinoma)", "Hepatocellular carcinoma, childhood onset", "Paediatric HCC (hepatocellular carcinoma)", "Pediatric hepatocellular carcinoma (disorder)", "Childhood-onset HCC (hepatocellular carcinoma)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pediatric hepatocellular carcinoma", "shortest_name_length": 13}
{"curie": "UMLS:C5206675", "names": ["Metastatic Malignant Neoplasm in the Head and Neck"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Malignant Neoplasm in the Head and Neck", "shortest_name_length": 50}
{"curie": "UMLS:C0743680", "names": ["Eye edema", "EYE EDEMA", "edema eye", "eye edema", "Eye oedema", "edema eyes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eye edema", "shortest_name_length": 9}
{"curie": "MONDO:0800084", "names": ["sclerosing bone dysplasia", "primary bone dysplasia with increased bone density", "primary osteodysplasia with increased bone density", "primary skeletal dysplasia with increased bone density"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary bone dysplasia with increased bone density", "shortest_name_length": 25}
{"curie": "UMLS:C5447546", "names": ["Refractory Ureter Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Ureter Urothelial Carcinoma", "shortest_name_length": 38}
{"curie": "UMLS:C1299260", "names": ["Metastatic Kaposi Sarcoma", "Kaposi sarcoma, metastatic", "Kaposi's sarcoma, metastatic", "Kaposi's sarcoma, metastatic (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kaposi's sarcoma, metastatic", "shortest_name_length": 25}
{"curie": "MONDO:0004329", "names": ["Pancreatic Intraductal Papillary-Mucinous Neoplasm, High Grade", "Pancreatic Intraductal Papillary-Mucinous Neoplasm, High-Grade", "pancreatic non-invasive intraductal papillary-mucinous carcinoma", "Pancreatic Non-Invasive Intraductal Papillary-Mucinous Carcinoma", "Pancreatic Intraductal Papillary-Mucinous Neoplasm with High Grade Dysplasia", "pancreatic intraductal papillary mucinous neoplasm with high grade dysplasia", "pancreatic intraductal papillary-mucinous neoplasm with high grade dysplasia", "Pancreatic Intraductal Papillary Mucinous Neoplasm with High Grade Dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic intraductal papillary-mucinous neoplasm with high grade dysplasia", "shortest_name_length": 62}
{"curie": "MONDO:0023164", "names": ["viral pericarditis", "pericarditis viral", "VIRAL PERICARDITIS", "PERICARDITIS VIRAL", "Viral pericarditis", "Viral Pericarditis", "virus; pericarditis", "pericarditis; viral", "pericarditis; virus", "viral; pericarditis", "Pericarditis viral NOS", "Viral pericarditis, NOS", "Viral pericarditis (disorder)", "viral pericarditis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "viral pericarditis", "shortest_name_length": 18}
{"curie": "MONDO:0006419", "names": ["Small Intestinal Dysplasia", "small intestinal dysplasia", "small intestinal intraepithelial neoplasia", "Small Intestinal Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small intestinal intraepithelial neoplasia", "shortest_name_length": 26}
{"curie": "UMLS:C1334320", "names": ["Kaposi Sarcoma NCI Grade 2", "Kaposi's Sarcoma NCI Grade 2", "Kaposi's Sarcoma NCI Grade II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kaposi Sarcoma NCI Grade 2", "shortest_name_length": 26}
{"curie": "MONDO:0024954", "names": ["visceral larva Migran", "Visceral Larva Migran", "larva visceral migrans", "Migran, visceral larva", "larva migrans visceral", "Visceral larva migrans", "Migran, Visceral Larva", "larva Migran, visceral", "Larva Migran, Visceral", "Visceral Larva Migrans", "visceral larva migrans", "Larva migrans, Visceral", "Visceral larval migrans", "Migrans, Visceral Larva", "larva migrans, visceral", "visceral; larva migrans", "Larva Migrans, Visceral", "migrans, visceral larva", "LARVA MIGRANS, VISCERAL", "Larva migrans visceralis", "larva migrans; visceralis", "visceral larva migrans syndrome", "Visceral larva migrans syndrome", "Visceral Larva Migrans Syndrome", "Toxocaral visceral larva migrans", "visceral larva migrans (diagnosis)", "Visceral larva migrans syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "larva migrans, visceral", "shortest_name_length": 21}
{"curie": "MONDO:0014163", "names": ["LVNC10", "CMD1MM", "cardiomyopathy, dilated, 1Mm", "CARDIOMYOPATHY, DILATED, 1MM", "LEFT VENTRICULAR NONCOMPACTION 10", "left ventricular noncompaction 10", "MYBPC3 left ventricular noncompaction", "left ventricular noncompaction type 10", "left ventricular noncompaction caused by mutation in MYBPC3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "left ventricular noncompaction 10", "shortest_name_length": 6}
{"curie": "MONDO:0032675", "names": ["CMS25", "myasthenic syndrome, congenital, 25", "myasthenic syndrome, congenital, 25, presynaptic", "MYASTHENIC SYNDROME, CONGENITAL, 25, PRESYNAPTIC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myasthenic syndrome, congenital, 25, presynaptic", "shortest_name_length": 5}
{"curie": "MONDO:0054739", "names": ["FRASRS3", "Fraser syndrome 3", "FRASER SYNDROME 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fraser syndrome 3", "shortest_name_length": 7}
{"curie": "UMLS:C5421324", "names": ["Locally Advanced Hypopharyngeal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Hypopharyngeal Carcinoma", "shortest_name_length": 41}
{"curie": "UMLS:C0280379", "names": ["nasopharynx lymphoepithelioma, stage I", "Nasopharyngeal lymphepithelioma stage I", "Nasopharyngeal lymphoepithelioma stage I", "Stage I Nasopharyngeal Lymphoepithelioma", "Stage I Lymphoepithelioma of Nasopharynx", "nasopharyngeal lymphoepithelioma, stage I", "Stage I Lymphoepithelioma of the Nasopharynx", "stage I lymphoepithelioma of the nasopharynx", "lymphoepithelioma of the nasopharynx, stage I", "Nasopharyngeal Undifferentiated Carcinoma Stage I", "Stage I Nasopharyngeal Undifferentiated Carcinoma", "Stage I Undifferentiated Nasopharyngeal Throat Cancer", "Stage I Nasopharyngeal Undifferentiated Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasopharyngeal lymphoepithelioma stage I", "shortest_name_length": 38}
{"curie": "MONDO:0006592", "names": ["parapsoriasis", "PARAPSORIASIS", "Parapsoriasis", "Parapsoriases", "parapsoriases", "Parapsoriasis, NOS", "digitate dermatosis", "Digitate Dermatoses", "Digitate Dermatosis", "Dermatoses, Digitate", "Dermatosis, Digitate", "parapsoriasis en plaque", "Parapsoriasis (disorder)", "parapsoriasis (diagnosis)", "Parapsoriasis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parapsoriasis", "shortest_name_length": 13}
{"curie": "MONDO:0030770", "names": ["CDDG2", "congenital disorder of deglycosylation 2", "CONGENITAL DISORDER OF DEGLYCOSYLATION 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital disorder of deglycosylation 2", "shortest_name_length": 5}
{"curie": "OMIM:614689", "names": ["SOLUBLE IL6R, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS", "SOLUBLE INTERLEUKIN-6 RECEPTOR, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 54}
{"curie": "MONDO:0019820", "names": ["univentricular cardiopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "univentricular cardiopathy", "shortest_name_length": 26}
{"curie": "UMLS:C1332868", "names": ["Cecum Non-Hodgkin Lymphoma", "Cecum Non-Hodgkin's Lymphoma", "Cecal Non-Hodgkin's Lymphoma", "Non-Hodgkin's Lymphoma of Cecum", "Non-Hodgkin's Lymphoma of the Cecum", "Primary Cecum Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cecum Non-Hodgkin Lymphoma", "shortest_name_length": 26}
{"curie": "MONDO:0010559", "names": ["SPG1", "Spg1", "L1 syndrome", "L1 Syndrome", "Masa Syndrome", "MASA syndrome", "MASA SYNDROME", "MASA Syndrome", "CRASH SYNDROME", "L1CAM syndrome", "CRASH Syndrome", "Crash syndrome", "CRASH syndrome", "spastic paraplegia 1", "Gareis-Mason syndrome", "GAREIS-MASON SYNDROME", "Gareis-Mason Syndrome", "Bianchine-Lewis syndrome", "MASA SYNDROME (disorder)", "adducted thumbs syndrome", "Spastic paraplegia, type 1", "Genetic Diseases, X-Linkeds", "Spastic Paraplegia, X-linked", "spastic paraplegia, X-linked", "X-linked spastic paraplegia 1", "SPASTIC PARAPLEGIA 1, X-LINKED", "spastic paraplegia 1, X-linked", "hereditary spastic paraplegia 1", "X-Linked Corpus Callosum Agenesis", "X-linked corpus callosum agenesis", "masa syndrome, X-linked recessive", "CRASH syndrome, X-linked recessive", "CLASPED THUMB AND MENTAL RETARDATION", "Clasped thumb and mental retardation", "Adducted thumb with mental retardation", "adducted thumb with mental retardation", "ADDUCTED THUMB WITH MENTAL RETARDATION", "Clasped thumb and intellectual disability", "mental retardation-clasped thumb syndrome", "clasped thumbs-mental retardation syndrome", "adducted thumbs-mental retardation syndrome", "adducted thumb with intellectual disability", "X-linked complicated spastic paraplegia type 1", "thumb congenital clasped with mental retardation", "thumb, congenital Clasped, with mental retardation", "Thumb, congenital clasped, with mental retardation", "THUMB, CONGENITAL CLASPED, WITH MENTAL RETARDATION", "congenital clasped thumbs-mental retardation syndrome", "thumb congenital clasped with intellectual disability", "thumb, congenital Clasped, with intellectual disability", "X-linked complicated hereditary spastic paraplegia type 1", "X-Linked Complicated Hereditary Spastic Paraplegia Type 1", "X-linked mental retardation-bilateral clasp thumb anomaly", "mental retardation aphasia shuffling Gait adducted thumbs (MASA)", "mental retardation, aphasia, shuffling Gait, and adducted thumbs", "Mental Retardation, Aphasia, Shuffling Gait, And Adducted Thumbs", "MENTAL RETARDATION, APHASIA, SHUFFLING GAIT, AND ADDUCTED THUMBS", "Mental retardation, Aphasia, Shuffling Gait, and Adducted Thumbs", "mental retardation-aphasia-shuffling gait-adducted thumbs syndrome", "Mental Retardation, Aphasia, Shuffling Gait, Adducted Thumbs (MASA)", "intellectual disability, aphasia, shuffling Gait, and adducted thumbs", "Mental retardation, adducted thumbs, shuffling gait, aphasia syndrome", "intellectual disability aphasia shuffling Gait adducted thumbs (MASA)", "X-Linked Hydrocephalus with Stenosis of the Aqueduct of Sylvius (Hsas)", "Intellectual disability-aphasia-shuffling gait-adducted thumbs syndrome", "intellectual disability-aphasia-shuffling gait-adducted thumbs syndrome", "mental retardation-aphasia-shuffling gait-adducted thumbs (MASA) syndrome", "Intellectual disability, aphasia, shuffling gait, adducted thumbs syndrome", "MASA (Mental Retardation, Aphasia, Shuffling Gait, Adducted Thumbs) Syndrome", "MASA (mental retardation, adducted thumbs, shuffling gait, aphasia) syndrome", "Intellectual disability, aphasia, shuffling gait, adducted thumbs syndrome (disorder)", "Corpus callosum hypoplasia-retardation-adducted thumbs-spasticity-hydrocephalus syndrome", "Hypoplasia of corpus callosum, intellectual disability, adducted thumbs, spasticity, hydrocephalus syndrome", "hypoplasia of corpus callosum and mental retardation with adducted thumbs and spasticity and hydrocephalus syndrome", "Hypoplasia of corpus callosum and mental retardation with adducted thumbs and spasticity and hydrocephalus syndrome", "Hypoplasia of corpus callosum, intellectual disability, adducted thumbs, spasticity, hydrocephalus syndrome (disorder)", "hypoplasia of corpus callosum and mental retardation with adducted thumbs and spasticity and hydrocephalus syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MASA syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0011787", "names": ["LGMD2I", "MDDGC5", "LGMDR9", "LGMD type 2I", "LGMD-FKRP related", "FKRP-related LGMD R9", "LGMD R9 FKRP-related", "LGMD due to FKRP deficiency", "limb-girdle muscular dystrophy type 2I", "muscular dystrophy limb-girdle type 2I", "Limb-girdle muscular dystrophy type 2I", "Limb girdle muscular dystrophy type 2I", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I", "muscular dystrophy, limb-girdle, type 2I", "Muscular Dystrophy, Limb-Girdle, Type 2I", "FKRP-related limb-girdle muscular dystrophy R9", "limb-girdle muscular dystrophy due to FKRP deficiency", "Limb-girdle muscular dystrophy due to FKRP deficiency", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 9", "FKRP autosomal recessive limb-girdle muscular dystrophy", "Autosomal recessive limb-girdle muscular dystrophy type 2I", "autosomal recessive limb-girdle muscular dystrophy type 2I", "Autosomal recessive limb girdle muscular dystrophy type 2I", "muscular dystrophy-dystroglycanopathy (limb-girdle) type C 5", "muscular dystrophy-dystroglycanopathy (Limb-girdle) type C, 5", "Muscular Dystrophy-Dystroglycanopathy (Limb-Girdle) Type C, 5", "muscular dystrophy-dystroglycanopathy limb-girdle FRKP-related", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5", "muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5", "muscular dystrophy-dystroglycanopathy, limb-girdle, Frkp-related", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, FRKP-RELATED", "Autosomal recessive limb girdle muscular dystrophy type 2I (disorder)", "Limb girdle muscular dystrophy due to deficiency of fukutin related protein", "autosomal recessive limb-girdle muscular dystrophy caused by mutation in FKRP"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive limb-girdle muscular dystrophy type 2I", "shortest_name_length": 6}
{"curie": "UMLS:C5205695", "names": ["Sinonasal Adenocarcinoma", "Nasal Cavity and Paranasal Sinus Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Adenocarcinoma", "shortest_name_length": 24}
{"curie": "MONDO:0030492", "names": ["SPGF59", "SPERMATOGENIC FAILURE 59", "spermatogenic failure 59"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 59", "shortest_name_length": 6}
{"curie": "MONDO:0020348", "names": ["AMSAN", "Acute motor-sensory axonal GBS", "acute motor-sensory axonal GBS", "Acute motor sensory axonal neuropathy", "Acute Motor-Sensory Axonal Neuropathy", "Acute motor-sensory axonal neuropathy", "acute motor-sensory axonal neuropathy", "Acute Motor and Sensory Axonal Neuropathy", "acute motor and sensory axonal neuropathy", "Acute motor and sensory axonal neuropathy", "Acute Motor And Sensory Axonal Neuropathy", "acute motor-sensory axonal Guillain-Barré syndrome", "Acute motor sensory axonal Guillain-Barré syndrome", "Acute motor-sensory axonal Guillain-Barré syndrome", "acute motor-sensory axonal Guillain-BarrC) syndrome", "Acute motor sensory axonal Guillain-Barré syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute motor and sensory axonal neuropathy", "shortest_name_length": 5}
{"curie": "MONDO:0007799", "names": ["HBD", "Hypophosphatemic Bone Disease", "hypophosphatemic bone disease", "HYPOPHOSPHATEMIC BONE DISEASE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypophosphatemic bone disease", "shortest_name_length": 3}
{"curie": "MONDO:0004361", "names": ["Spinal Cord Ependymoma", "spinal cord ependymoma", "Adult Spinal Ependymoma", "adult spinal cord ependymoma", "Adult Spinal Cord Ependymoma", "spinal cord ependymoma of adults", "Adult Spinal Cord Ependymoma without MYCN Amplification"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult spinal cord ependymoma", "shortest_name_length": 22}
{"curie": "MONDO:0001175", "names": ["water clefts", "Water clefts", "cataract immature", "Immature cataract", "immature cataract", "Incipient cataract", "Cataract, immature", "incipient cataract", "Incipient Cataract", "Cataract, immature NOS", "incipient senile cataract", "Incipient senile cataract", "Senile incipient cataract", "cataract; senile, incipient", "senile; cataract, incipient", "incipient; cataracta senilis", "Immature cataract (disorder)", "immature cataract (diagnosis)", "Incipient cataract (disorder)", "Incipient senile cataract (disorder)", "immature cataract (physical finding)", "incipient senile cataract (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immature cataract", "shortest_name_length": 12}
{"curie": "MONDO:0004142", "names": ["Lung Combined Large Cell Neuroendocrine Carcinoma", "lung combined large cell neuroendocrine carcinoma", "Combined Lung Large Cell Neuroendocrine Carcinoma", "Combined Large Cell Lung Neuroendocrine Carcinoma", "combined large cell lung neuroendocrine carcinoma", "Combined Large Cell Neuroendocrine Carcinoma of Lung", "combined large cell neuroendocrine carcinoma of lung", "Pulmonary Combined Large Cell Neuroendocrine Carcinoma", "pulmonary combined large cell neuroendocrine carcinoma", "pulmonary Combined large cell neuroendocrine carcinoma", "combined large cell neuroendocrine carcinoma of the lung", "Combined Large Cell Neuroendocrine Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung combined large cell neuroendocrine carcinoma", "shortest_name_length": 49}
{"curie": "MONDO:0007640", "names": ["SFD", "Sorsby fundus dystrophy", "SORSBY FUNDUS DYSTROPHY", "Sorsby's fundus dystrophy", "hemorrhagic macular dystrophy", "macular dystrophy, hemorrhagic", "MACULAR DYSTROPHY, HEMORRHAGIC", "Macular Dystrophy, Hemorrhagic", "Pseudoinflammatory macular dystrophy", "Sorsby pseudoinflammatory fundus dystrophy", "pseudoinflammatory fundus dystrophy of Sorsby", "Sorsby's pseudoinflammatory macular dystrophy", "fundus dystrophy, pseudoinflammatory, of Sorsby", "FUNDUS DYSTROPHY, PSEUDOINFLAMMATORY, OF SORSBY", "Fundus Dystrophy, Pseudoinflammatory, Of Sorsby", "Sorsby pseudoinflammatory fundus dystrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sorsby fundus dystrophy", "shortest_name_length": 3}
{"curie": "MONDO:0005963", "names": ["Sparganosis", "SPARGANOSIS", "sparganosis", "Sparganoses", "spirometrosis", "Spirometrosis", "Spirometriosis", "infection by sparganum", "Infection by Sparganum", "sparganosis (diagnosis)", "larval; Dibothriocephalus", "Dibothriocephalus; larval", "Larval diphyllobothriasis", "diphyllobothriasis; larval", "larval; diphyllobothriasis", "Larval dibothriocephaliasis", "Spirometra infectious disease", "Infection by Spirometra larvae", "Spirometra disease or disorder", "Infection by Diphyllobothrium larvae", "Infection caused by Spirometra larvae", "infestation; Diphyllobothrium, larval", "Spirometra caused disease or disorder", "Diphyllobothrium; infestation, larval", "Dibothriocephalus; infestation, larval", "infestation; Dibothriocephalus, larval", "Sparganosis - larval diphyllobothriasis", "Sparganosis [larval diphyllobothriasis]", "sparganosis [larval diphyllobothriasis]", "Sparganosis (larval diphyllobothriasis)", "Infection caused by Spirometra larvae (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sparganosis", "shortest_name_length": 11}
{"curie": "MONDO:0032904", "names": ["MECD2", "meesmann corneal dystrophy 2", "Meesmann corneal dystrophy 2", "CORNEAL DYSTROPHY, MEESMANN, 2", "corneal dystrophy, Meesmann, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal dystrophy, Meesmann, 2", "shortest_name_length": 5}
{"curie": "MONDO:0017695", "names": ["GSDIV, progressive hepatic form", "GSD type 4, progressive hepatic form", "GBE deficiency, progressive hepatic form", "glycogenosis type 4, progressive hepatic form", "glycogenosis type IV, progressive hepatic form", "glycogen storage disease type 4, progressive hepatic form", "glycogen storage disease type IV, progressive hepatic form", "GSD due to glycogen branching enzyme deficiency, progressive hepatic form", "glycogenosis due to glycogen branching enzyme deficiency, progressive hepatic form", "glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form", "shortest_name_length": 31}
{"curie": "MONDO:0017456", "names": ["mirror hand", "Central polydactyly", "central polydactyly", "mesoaxial polydactyly", "Mesoaxial polydactyly", "Insertional polydactyly", "Intercalary polydactyly", "central polydactyly of hand", "Central polydactyly of fingers", "central polydactyly of fingers", "mesoaxial polydactyly of fingers", "Mesoaxial polydactyly of fingers", "Central polydactyly of fingers (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central polydactyly of fingers", "shortest_name_length": 11}
{"curie": "UMLS:C0751112", "names": ["subclinical seizure", "Subclinical Seizure", "Seizure, Subclinical", "Subclinical Seizures", "subclinical seizures", "Seizures, Subclinical"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subclinical Seizure", "shortest_name_length": 19}
{"curie": "MONDO:0011840", "names": ["CMD1M", "dilated cardiomyopathy 1M", "Cardiomyopathy, Dilated, 1M", "CARDIOMYOPATHY, DILATED, 1M", "cardiomyopathy, dilated, 1M", "dilated cardiomyopathy type 1M", "cardiomyopathy, dilated, type 1M", "CSRP3 familial isolated dilated cardiomyopathy", "familial isolated dilated cardiomyopathy caused by mutation in CSRP3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1M", "shortest_name_length": 5}
{"curie": "MONDO:0015200", "names": ["Anisakis", "ANISAKIASIS", "Anisakiasis", "Anisakiosis", "Anisakiases", "anisakiasis", "Anisakis Infection", "Anisakis infection", "Herringworm disease", "Infection, Anisakis", "Anisakis Infections", "Infections, Anisakis", "Herring worm disease", "HERRING WORM DISEASE", "infestation; Anisakis", "Anisakis; infestation", "anisakiasis (diagnosis)", "Pseudoterranova infection", "Anisakis simplex infection", "infection by Anisakis larva", "Infection by Anisakis larva", "infections, Anisakis simplex", "Infection caused by Anisakis larva", "Infection caused by Anisakis larva (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anisakiasis", "shortest_name_length": 8}
{"curie": "MONDO:0013340", "names": ["PARK5", "UCHL1 young-onset Parkinson disease", "Parkinson disease 5, susceptibility to", "PARKINSON DISEASE 5, AUTOSOMAL DOMINANT", "susceptibility to autosomal dominant Parkinson disease 5", "young-onset Parkinson disease caused by mutation in UCHL1", "Parkinson disease 5, autosomal dominant, susceptibility to", "PARKINSON DISEASE 5, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parkinson disease 5, autosomal dominant, susceptibility to", "shortest_name_length": 5}
{"curie": "MONDO:0002173", "names": ["Neuroma", "neuroma", "NEUROMA", "Neuromas", "neuromas", "Nerve tumor", "Neuroma NOS", "nerve pinch", "Neuroma, NOS", "Nerve tumour", "Crushed nerve", "Pinched nerve", "pinched nerve", "nerve pinching", "NERVE COMPRESSION", "nerve compression", "Nerve compression", "nerve; compression", "compression; nerve", "Neuroma (disorder)", "compression of nerve", "Compression of nerve", "nerve compression injury", "Compression injury of nerve", "compression injury of nerve", "Neuroma (morphologic abnormality)", "Compression injury of nerve (disorder)", "A tumor made up of nerve cells and nerve fibers"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuroma", "shortest_name_length": 7}
{"curie": "MONDO:0700022", "names": ["chromosome 15 disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 15 disorder", "shortest_name_length": 22}
{"curie": "UMLS:C0948873", "names": ["flu symptom", "Flu symptoms", "symptoms flu", "flu symptoms"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Flu symptoms", "shortest_name_length": 11}
{"curie": "MONDO:0021229", "names": ["Ciliary body mass", "Ciliary Body Tumor", "ciliary body tumor", "Tumor of ciliary body", "tumor of ciliary body", "Ciliary Body Neoplasm", "ciliary body neoplasm", "Tumor of Ciliary Body", "Tumour of ciliary body", "Neoplasm of ciliary body", "Neoplasm of Ciliary Body", "neoplasm of ciliary body", "eye neoplasm ciliary body", "Tumor of the Ciliary Body", "tumor of the ciliary body", "Neoplasm of the Ciliary Body", "neoplasm of the ciliary body", "ciliary body neoplasm (disease)", "Neoplasm of ciliary body (disorder)", "Neoplasm of ciliary body (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ciliary body neoplasm", "shortest_name_length": 17}
{"curie": "MONDO:0006565", "names": ["juvenile dermatitis herpetiformis", "Juvenile dermatitis herpetiformis", "herpetiformis; dermatitis, juvenile", "dermatitis; herpetiformis, juvenile", "Benign chronic vesiculobullous dermatosis of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile dermatitis herpetiformis", "shortest_name_length": 33}
{"curie": "UMLS:C0280356", "names": ["Stage III Mouth Mucoepidermoid Carcinoma", "Stage III Oral Cavity Mucoepidermoid Cancer", "Stage III Mucoepidermoid Carcinoma of Mouth", "Stage III Oral Cavity Mucoepidermoid Carcinoma", "Stage III Mucoepidermoid Carcinoma of the Mouth", "oral cavity mucoepidermoid carcinoma, stage III", "Stage III Mucoepidermoid Carcinoma of Oral Cavity", "Stage III Mucoepidermoid Carcinoma of the Oral Cavity", "stage III mucoepidermoid carcinoma of the oral cavity", "Mucoepidermoid carcinoma of the oral cavity stage III", "Stage III Oral Cavity Mucoepidermoid Carcinoma AJCC v7", "Stage III Oral Cavity Mucoepidermoid Carcinoma AJCC v6", "mucoepidermoid carcinoma of the oral cavity, stage III", "Stage III Oral Cavity Mucoepidermoid Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mucoepidermoid carcinoma of the oral cavity stage III", "shortest_name_length": 40}
{"curie": "MONDO:0007935", "names": ["MDDC", "CYMD", "DCMD", "Mddc", "cystoid macular edema", "cystoid edema macular", "Cystoid Macular Edema", "Cystoid macular edema", "cystoid macular oedema", "Familial macular edema", "familial macular edema", "macular edema, cystoid", "Cystoid macular oedema", "Macular Edema, Cystoid", "MACULAR EDEMA, CYSTOID", "Edema, Cystoid Macular", "Cystoid macular dystrophy", "cystoid macular dystrophy", "Cystoid Macular Dystrophy", "CYSTOID MACULAR DYSTROPHY", "CMO - cystoid macular edema", "CME - cystoid macular edema", "CMO - cystoid macular oedema", "CME - cystoid macular oedema", "Central Retinal Edema, Cystoid", "Cystoid macular edema (disorder)", "cystoid macular edema (diagnosis)", "macular dystrophy, dominant cystoid", "MACULAR DYSTROPHY, DOMINANT CYSTOID", "Macular Dystrophy, Dominant Cystoid", "cystoid macular edema autosomal dominant", "Autosomal dominant cystoid macular edema", "autosomal dominant cystoid macular edema", "Autosomal dominant cystoid macular oedema", "Autosomal dominant cystoid macular edema (disorder)", "Autosomal dominant cystoid macular edema (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cystoid macular edema", "shortest_name_length": 4}
{"curie": "UMLS:C4727411", "names": ["Recurrent Parotid Gland Adenoid Cystic Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Parotid Gland Adenoid Cystic Carcinoma", "shortest_name_length": 48}
{"curie": "UMLS:C4054226", "names": ["Pauci-immune Glomerulonephritis - ANCA Negative", "Pauci-Immune Glomerulonephritis - ANCA Negative"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pauci-Immune Glomerulonephritis - ANCA Negative", "shortest_name_length": 47}
{"curie": "UMLS:C1263992", "names": ["Toxic methemoglobinemia with cyanosis", "Toxic Methemoglobinemia with Cyanosis", "Toxic methaemoglobinaemia with cyanosis", "Toxic methemoglobinemia with cyanosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Toxic methemoglobinemia with cyanosis", "shortest_name_length": 37}
{"curie": "UMLS:C4524960", "names": ["Small Intestinal Adenocarcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Intestinal Adenocarcinoma by AJCC v8 Stage", "shortest_name_length": 48}
{"curie": "MONDO:0010511", "names": ["CBAVDX", "X-linked congenital bilateral absence of vas deferens", "congenital bilateral absence of vas deferens, X-linked", "vas deferens, congenital bilateral aplasia of, X-linked", "VAS DEFERENS, CONGENITAL BILATERAL APLASIA OF, X-LINKED", "vas deferens, congenital bilateral aplasia of, X-linked; CBAVDX"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vas deferens, congenital bilateral aplasia of, X-linked", "shortest_name_length": 6}
{"curie": "MONDO:0001515", "names": ["corneal degeneration", "Corneal Degeneration", "Corneal degeneration", "cornea; degeneration", "degeneration; cornea", "Corneal degenerations", "corneal degenerations", "Corneal degeneration, NOS", "Corneal degeneration (disorder)", "Unspecified corneal degeneration", "corneal degeneration (diagnosis)", "Corneal degeneration, unspecified", "corneal degeneration (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal degeneration", "shortest_name_length": 20}
{"curie": "UMLS:C0235560", "names": ["Airway hemorrhage", "Airway haemorrhage", "Respiratory tract bleeding", "RESPIRATORY TRACT HEMORRHAGE", "Respiratory Tract Hemorrhage", "Respiratory tract hemorrhage", "RESPIRATORY TRACT HAEMORRHAGE", "Respiratory tract haemorrhage", "Respiratory tract hemorrhage NOS", "Respiratory tract hemorrhage, NOS", "Respiratory tract haemorrhage NOS", "Respiratory tract haemorrhage, NOS", "Respiratory tract hemorrhage (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Respiratory tract hemorrhage", "shortest_name_length": 17}
{"curie": "MONDO:0007039", "names": ["NF2", "ACN", "BANF", "Neurofibromatosis 2", "neurofibromatosis 2", "neurofibromatosis ii", "Neurofibromatosis II", "Neurofibromatosis IIs", "Neurofibromatosis type 2", "Type 2 Neurofibromatosis", "Type 2 Neurofibromatoses", "type 2 neurofibromatosis", "neurofibromatosis type 2", "Neurofibromatosis Type 2", "neurofibromatosis, type 2", "Familial acoustic neuroma", "Neurofibromatosis, type 2", "Neurofibromatosis Type II", "Central Neurofibromatosis", "NF2 (Neurofibromatosis 2)", "central neurofibromatosis", "Central Neurofibromatoses", "neurofibromatosis type II", "Type II Neurofibromatosis", "Neurofibromatoses, Type 2", "neurofibromatosis type ii", "Neurofibromatosis, Type 2", "Type II Neurofibromatoses", "Neurofibromatosis, Central", "Acoustic neurofibromatosis", "Neurofibromatoses, Type II", "Acoustic Neurofibromatosis", "NEUROFIBROMATOSIS, TYPE II", "NF2s (Neurofibromatosis 2)", "familial acoustic neuromas", "acoustic neurofibromatosis", "Neurofibromatosis, Type II", "Neurofibromatoses, Central", "neurofibromatosis, type II", "Bilateral acoustic neuromas", "Bilateral Acoustic Neurinoma", "Neuroma, Acoustic, Bilateral", "acoustic neurinoma bilateral", "bilateral acoustic neurinoma", "Acoustic Neurinoma, Bilateral", "Bilateral Acoustic Schwannoma", "Central NF2 Neurofibromatoses", "Neurinoma, Bilateral Acoustic", "Central NF2 Neurofibromatosis", "Bilateral Acoustic Neurinomas", "ACOUSTIC NEURINOMA, BILATERAL", "acoustic neurinoma, bilateral", "Acoustic Schwannoma, Bilateral", "Neurofibromatoses, Central NF2", "Bilateral Acoustic Schwannomas", "Familial vestibular schwannoma", "neurofibromatosis central type", "Neurofibromatosis, Central NF2", "acoustic schwannomas bilateral", "bilateral acoustic schwannomas", "Acoustic Neurinomas, Bilateral", "Schwannoma, Bilateral Acoustic", "Neurinomas, Bilateral Acoustic", "Bilateral vestibular schwannoma", "Acoustic Schwannomas, Bilateral", "Schwannoma, Acoustic, Bilateral", "ACOUSTIC SCHWANNOMAS, BILATERAL", "Schwannomas, Bilateral Acoustic", "NEUROFIBROMATOSIS, CENTRAL TYPE", "Neurofibromatosis, Central, NF2", "acoustic Schwannomas, bilateral", "Neurofibromatosis, central type", "neurofibromatosis, central type", "Neurofibromatosis, Central, NF 2", "Neurofibromatosis type 2 (disorder)", "Bilateral Acoustic Neurofibromatosis", "Bilateral acoustic neurofibromatosis", "BILATERAL ACOUSTIC NEUROFIBROMATOSIS", "Bilateral Acoustic Neurofibromatoses", "bilateral acoustic neurofibromatosis", "Neurofibromatosis, Bilateral Acoustic", "Acoustic Neurofibromatosis, Bilateral", "Acoustic Neurofibromatoses, Bilateral", "neurofibromatosis type II (diagnosis)", "Neurofibromatoses, Bilateral Acoustic", "Neurofibromatosis, Acoustic, Bilateral", "BANF - Bilateral acoustic neurofibromatosis", "Neurofibromatosis, type 2 [acoustic neurofibromatosis]", "Neurofibromatosis, type 2 (acoustic neurofibromatosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurofibromatosis type 2", "shortest_name_length": 3}
{"curie": "MONDO:0015923", "names": ["acquired peripheral neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired peripheral neuropathy", "shortest_name_length": 30}
{"curie": "MONDO:0020283", "names": ["uveitis", "Uveitis", "UVEITIS", "Uveitides", "Uveitis NOS", "Uveitis, NOS", "uveitis (disease)", "uvea inflammation", "Uveitis (disorder)", "uvea; inflammation", "Uveal inflammation", "uveitis (diagnosis)", "uveitis was present", "inflammation of uvea", "Intraocular inflammation", "uveitis (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uveitis", "shortest_name_length": 7}
{"curie": "MONDO:0019005", "names": ["Nephronopthisis", "nephronopthisis", "nephronophthisis", "Nephronophthisis", "medullary; cystic", "MEDULLARY CYSTIC KIDNEY", "medullary cystic kidney", "Medullary cystic kidney", "MEDULLARY CYSTIC DISEASE", "Medullary cystic disease", "medullary cystic disease", "cystic kidneys medullary", "cystic disease medullary", "kidney; cystic, medullary", "juvenile nephronophthisis", "cystic; kidney, medullary", "nephronophthisis (disease)", "Nephronophthisis (disorder)", "medullary cystic kidney disease", "Medullary cystic kidney disease", "Familial juvenile nephrophthisis", "NEPHRONOPTHISIS, FAMILIAL JUVENILE", "Familial juvenile nephronophthisis", "Medullary cystic disease (disorder)", "Medullary cystic disease of the kidney", "medullary cystic kidney disease (diagnosis)", "Autosomal recessive medullary cystic disease", "Familial juvenile medullary cystic kidney disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephronophthisis", "shortest_name_length": 15}
{"curie": "MONDO:0010465", "names": ["KABUK2", "KABUKI SYNDROME 2", "Kabuki syndrome 2", "KABUKI syndrome 2", "Kabuki syndrome type 2", "Kabuki syndrome 2, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kabuki syndrome 2", "shortest_name_length": 6}
{"curie": "MONDO:0003452", "names": ["cochlea disease", "Cochlear Disease", "cochlear disease", "Cochlear Diseases", "cochlear disorder", "Disease, Cochlear", "Diseases, Cochlear", "disease of cochlea", "disorder of cochlea", "cochlea disease or disorder", "disease or disorder of cochlea"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cochlear disorder", "shortest_name_length": 15}
{"curie": "MONDO:0016848", "names": ["JTA", "JGCA", "JPMR", "juvenile cranial arteritis", "Juvenile Temporal Arteritis", "Juvenile temporal arteritis", "juvenile temporal arteritis", "Temporal Arteritis, Juvenile", "Arteritis, Juvenile Temporal", "Juvenile Temporal Arteritides", "juvenile giant cell arteritis", "Arteritides, Juvenile Temporal", "Temporal Arteritides, Juvenile", "juvenile polymyalgia rheumatica", "Juvenile temporal arteritis (disorder)", "Non-giant cell granulomatous temporal arteritis with eosinophilia", "non-giant cell granulomatous temporal arteritis with eosinophilia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile temporal arteritis", "shortest_name_length": 3}
{"curie": "MONDO:0100504", "names": ["fungal infection of the toenail"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fungal infection of the toenail", "shortest_name_length": 31}
{"curie": "UMLS:C5420339", "names": ["Parotid Gland Nodular Fasciitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parotid Gland Nodular Fasciitis", "shortest_name_length": 31}
{"curie": "UMLS:C0276026", "names": ["Pneumonia due to H. influenzae", "Hemophilus influenza pneumonia", "Hemophilus Influenzae Pneumonia", "Hemophilus influenzae pneumonia", "PNEUMONIA, HEMOPHILUS INFLUENZA", "haemophilus influenza pneumonia", "Haemophilus influenza pneumonia", "Hemophilus influenzae; pneumonia", "haemophilus influenzae pneumonia", "Haemophilus influenzae pneumonia", "pneumonia; Hemophilus influenzae", "Haemophilus influenzae; pneumonia", "pneumonia; Haemophilus influenzae", "Pneumonia due to Hemophilus influenzae", "pneumonia due to Haemophilus influenzae", "Pneumonia due to Haemophilus influenzae", "PNEUMONIA BACTERIAL HEMOPHILUS INFLUENZA", "Haemophilus influenzae pneumonia (disorder)", "pneumonia due to Haemophilus influenzae (diagnosis)", "Pneumonia due to Hemophilus influenzae [H. influenzae]", "Pneumonia due to Hemophilus Influenzae (H. influenzae)", "Pneumonia due to Hemophilus influenzae (H. influenzae)", "Pneumonia due to Haemophilus influenzae (H. influenzae)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Haemophilus influenzae pneumonia", "shortest_name_length": 30}
{"curie": "MONDO:0007338", "names": ["Cleft velum", "cleft velum", "CLEFT SOFT PALATE", "Cleft soft palate", "soft cleft palate", "cleft soft palate", "Cleft Soft Palate", "Cleft palate (soft)", "cleft; palate, soft", "Cleft of soft palate", "Cleft muscular palate", "Cleft velum palatinum", "cleft velum palatinum", "Cleft of soft palate only", "Cleft soft palate, central", "Cleft of soft palate (disorder)", "Cleft of soft palate (diagnosis)", "cleft soft palate (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleft soft palate", "shortest_name_length": 11}
{"curie": "MONDO:0018991", "names": ["Hepatoportal sclerosis", "hepatoportal sclerosis", "obliterative portal venopathy", "Obliterative portal venopathy", "Hepatoportal sclerosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatoportal sclerosis", "shortest_name_length": 22}
{"curie": "MONDO:0011600", "names": ["CMS4A", "CMS1A1", "CMS Ia1", "Cms Ia1", "CMS1A1, FORMERLY", "Cms Ia1, formerly", "CMS Ia1, FORMERLY", "MYASTHENIA, FAMILIAL INFANTILE, 1", "Myasthenia, Familial Infantile, 1", "congenital myasthenic syndrome 4A", "congenital myasthenic syndrometype Ia1", "congenital myasthenic syndrome type 4A", "congenital myasthenic syndrome type Ia1", "Congenital Myasthenic Syndrome Type Ia1", "congenital myasthenic syndrome 4A slow-channel", "myasthenic syndrome, congenital, 4A, slow-channel", "CONGENITAL MYASTHENIC SYNDROME TYPE Ia1, FORMERLY", "MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL", "congenital myasthenic syndrome type Ia1, formerly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myasthenic syndrome 4A", "shortest_name_length": 5}
{"curie": "MONDO:0000618", "names": ["HER2- breast cancer", "HER2 negative breast cancer", "HER2-negative breast cancer", "HER2 negative breast carcinoma", "HER2-Negative Breast Carcinoma", "HER2 Negative Breast Carcinoma", "HER2/neu-negative breast cancer", "HER2 Negative Breast Adenocarcinoma", "Her2-receptor negative breast cancer", "Human epidermal growth factor 2 negative carcinoma of breast", "breast neoplasm malignant human epidermal growth factor 2 negative", "Human epidermal growth factor 2 (HER2) negative carcinoma of breast", "Human epidermal growth factor 2 negative carcinoma of breast (disorder)", "Human epidermal growth factor 2 negative carcinoma of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Her2-receptor negative breast cancer", "shortest_name_length": 19}
{"curie": "UMLS:C0877072", "names": ["Cytomegalovirus chorioretinitis", "Chorioretinitis caused by Cytomegalovirus", "Chorioretinitis caused by Cytomegalovirus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cytomegalovirus chorioretinitis", "shortest_name_length": 31}
{"curie": "UMLS:C0280372", "names": ["Stage III Oropharyngeal SCC", "Stage III SCC of Oropharynx", "Stage III SCC of the Oropharynx", "Stage III Oropharyngeal Epidermoid Carcinoma", "Stage III Epidermoid Carcinoma of Oropharynx", "oropharynx squamous cell carcinoma, stage III", "Oropharyngeal squamous cell carcinoma stage III", "Stage III Oropharyngeal Squamous Cell Carcinoma", "Stage III Squamous Cell Carcinoma of Oropharynx", "Stage III Epidermoid Carcinoma of the Oropharynx", "oropharyngeal squamous cell carcinoma, stage III", "epidermoid carcinoma of the oropharynx, stage III", "Stage III Squamous Cell Carcinoma of the Oropharynx", "stage III squamous cell carcinoma of the oropharynx", "Stage III Oropharyngeal Throat Squamous Cell Cancer", "squamous cell carcinoma of the oropharynx, stage III", "Stage III Oropharyngeal Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oropharyngeal squamous cell carcinoma stage III", "shortest_name_length": 27}
{"curie": "MONDO:0021682", "names": ["Viral Venereal Disease", "viral venereal disease", "viral venereal diseases", "Viral Venereal Diseases", "disease, viral venereal", "Disease, Viral Venereal", "venereal disease, viral", "Venereal Disease, Viral", "diseases, viral venereal", "Diseases, Viral Venereal", "venereal diseases, viral", "Venereal Diseases, Viral", "Viral Sexually Transmitted Disease", "viral sexually transmitted disease", "Sexually Transmitted Disease, Viral", "Viral Sexually Transmitted Diseases", "sexually Transmitted disease, viral", "viral sexually Transmitted diseases", "Sexually Transmitted Diseases, Viral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "viral sexually transmitted disease", "shortest_name_length": 22}
{"curie": "MONDO:0016943", "names": ["trisomy 6p", "Trisomy 6p", "6p trisomy", "6p duplication", "Duplication 6p", "partial trisomy 6p", "Chromosome 6, trisomy 6p", "chromosome 6p duplication", "partial trisomy of chromosome 6p", "partial duplication of chromosome 6p", "partial trisomy of the short arm of chromosome 6", "partial duplication of the short arm of chromosome 6", "partial duplication of the short arm of chromosome type 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of the short arm of chromosome 6", "shortest_name_length": 10}
{"curie": "MONDO:0044624", "names": ["pediatric collagenous gastritis", "childhood-onset collagenous gastritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pediatric collagenous gastritis", "shortest_name_length": 31}
{"curie": "MONDO:0002656", "names": ["CARCINOMA SKIN", "SKIN CARCINOMA", "Carcinoma skin", "Skin carcinoma", "Skin Carcinoma", "Carcinoma;skin", "skin carcinoma", "carcinomas skin", "CARCINOMA OF SKIN", "Carcinoma of Skin", "carcinoma of skin", "Skin carcinoma NOS", "carcinoma of the skin", "Carcinoma of the Skin", "zone of skin carcinoma", "nonmelanoma skin cancer", "Nonmelanoma skin cancer", "cancer nonmelanoma skin", "Non-Melanoma Skin Cancer", "non-melanoma skin cancer", "cancers nonmelanoma skin", "Non-melanoma Skin Cancer", "skin cancer, non-melanoma", "carcinoma of zone of skin", "Skin Cancer, Non-Melanoma", "Skin cancer (non-melanoma)", "non-melanoma cancer of skin", "Non-Melanoma Cancer of Skin", "carcinoma of skin (diagnosis)", "Cancer of skin (excl melanoma)", "non-melanoma cancer of the skin", "Non-Melanoma Cancer of the Skin", "Cancer of skin (excluding melanoma)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin carcinoma", "shortest_name_length": 14}
{"curie": "MONDO:0008791", "names": ["ANPH", "ANPH1", "Anencephaly", "anencephaly", "ANENCEPHALY", "Anencephalus", "anencephalus", "ANENCEPHALUS", "ANENCEPHALIA", "Anencephalia", "anencephalia", "Anencephalias", "anencephaly 1", "ANENCEPHALY 1", "brain; absent", "brain aplasia", "aplasia; brain", "absence; brain", "brain; aplasia", "agenesis; brain", "brain; agenesis", "Fetal anencephaly", "agenesis of brain", "Agenesis of brain", "Foetal anencephaly", "Anencephalic monster", "Isolated anencephaly", "Embryonic anencephaly", "Anencephalus (disorder)", "anencephaly (diagnosis)", "Brain Congenital Absence", "Congenital absence of brain", "Congenital Absence of Brain", "Absence of Brain, Congenital", "Fetal anencephaly (disorder)", "agenesis of brain (diagnosis)", "isolated anencephaly/exencephaly", "absence of a large part of the brain and the skull"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anencephaly 1", "shortest_name_length": 4}
{"curie": "MONDO:0004989", "names": ["Breast Cancer", "Breast cancer", "breast cancer", "cancer, breast", "Breast Carcinoma", "breast carcinoma", "BREAST CARCINOMA", "Carcinoma breast", "Cancer of Breast", "cancer of breast", "Breast carcinoma", "CARCINOMA BREAST", "Carcinoma, Breast", "Mammary carcinoma", "BREAST, CARCINOMA", "Mammary Carcinoma", "Breast Carcinomas", "mammary carcinoma", "breast carcinomas", "Breast cancer, NOS", "breast cancer, NOS", "Carcinomas, Breast", "CARCINOMA OF BREAST", "Carcinoma of Breast", "carcinoma of breast", "Carcinoma of breast", "Cancer of the Breast", "cancer of the breast", "Breast carcinoma NOS", "breast cancer diagnosis", "carcinoma of the breast", "Carcinoma of the Breast", "CA - Carcinoma of breast", "BREAST CANCER, CARCINOMA", "Carcinoma of breast (disorder)", "carcinoma of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast carcinoma", "shortest_name_length": 13}
{"curie": "UMLS:C3274531", "names": ["Airway Hemangioma", "Airway Infantile Hemangioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Airway Infantile Hemangioma", "shortest_name_length": 17}
{"curie": "MONDO:0010973", "names": ["DFNA5", "autosomal dominant deafness 5", "DEAFNESS, AUTOSOMAL DOMINANT 5", "Deafness, Autosomal Dominant 5", "deafness, autosomal dominant 5", "deafness, autosomal dominant type 5", "DEAFNESS, AUTOSOMAL DOMINANT 5 (disorder)", "autosomal dominant nonsyndromic deafness 5", "GSDME autosomal dominant nonsyndromic deafness", "autosomal dominant nonsyndromic hearing loss 5", "autosomal dominant nonsyndromic deafness type 5", "autosomal dominant nonsyndromic deafness caused by mutation in GSDME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 5", "shortest_name_length": 5}
{"curie": "MONDO:0008876", "names": ["BS", "BLM", "BLS", "BSyn", "Bloom", "MGRISCE1", "Bloom syndrome", "Bloom Syndrome", "bloom syndrome", "BLOOM SYNDROME", "blooms syndrome", "Bloom's Syndrome", "Bloom's syndrome", "bloom's syndrome", "Bloom's Syndromes", "BS - Bloom syndrome", "Bloom syndrome (disorder)", "Bloom's syndrome (diagnosis)", "Bloom-Torre-Machacek syndrome", "Bloom Torre Machacek Syndrome", "Bloom-Torre-Machacek Syndrome", "Congenital telangiectatic erythema", "Congenital Telangiectatic Erythema", "congenital telangiectatic erythema", "Congenital Telangiectatic Erythemas", "Telangiectatic Erythema, Congenital", "Erythema, Congenital Telangiectatic", "Congenital Telangiectatic Erythema syndrome", "Congenital Telangiectatic Erythema Syndrome", "congenital telangiectatic erythema syndrome", "Congenital telangiectatic erythema syndrome", "microcephaly, growth restriction, and increased sister chromatid exchange 1", "MICROCEPHALY, GROWTH RESTRICTION, AND INCREASED SISTER CHROMATID EXCHANGE 1", "growth deficiency, sun-sensitive, telangiectatic, hypo and hyperpigmented skin, predisposition to malignancy and chromosomal instability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bloom syndrome", "shortest_name_length": 2}
{"curie": "UMLS:C4724930", "names": ["Unresectable Skin Melanoma", "Unresectable Melanoma of Skin", "Unresectable Cutaneous Melanoma", "Unresectable Cutaneous (Skin) Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Cutaneous Melanoma", "shortest_name_length": 26}
{"curie": "MONDO:0006008", "names": ["epidemic vertigo", "Epidemic vertigo", "Vestibular Neuritis", "Vestibular neuritis", "vestibular neuritis", "Neuritis, Vestibular", "vestibular neuronitis", "Vestibular Neuritides", "Vestibular neuronitis", "Vestibular neuropathy", "Vestibular Neuronitis", "VESTIBULAR NEURONITIS", "Neuritides, Vestibular", "Neuronitis, Vestibular", "neuronitis; vestibular", "vestibular; neuronitis", "Acute epidemic vertigo", "Vestibular Neuronitides", "Neuronitides, Vestibular", "Acute Vestibular Neuritis", "Vestibular Nerve Neuritis", "Neuritis, Acute Vestibular", "Nerve Neuritis, Vestibular", "Vestibular Neuritis, Acute", "Neuritis, Vestibular Nerve", "Epidemic Neurolabyrinthitis", "Acute vestibular neuronitis", "epidemic neurolabyrinthitis", "Acute Vestibular Neuritides", "Epidemic neurolabyrinthitis", "Vestibular Nerve Neuritides", "Epidemic vertigo (disorder)", "Neurolabyrinthitis, Epidemic", "Vestibular Neuritides, Acute", "epidemic vertigo (diagnosis)", "Neuritides, Acute Vestibular", "Neuritides, Vestibular Nerve", "Nerve Neuritides, Vestibular", "Epidemic Neurolabyrinthitides", "Vestibular Nerve Inflammation", "Inflammation, Vestibular Nerve", "Vestibular Nerve Inflammations", "Nerve Inflammation, Vestibular", "Neurolabyrinthitides, Epidemic", "Nerve Inflammations, Vestibular", "Inflammations, Vestibular Nerve", "Acute peripheral vestibulopathy", "Acute Peripheral Vestibulopathy", "acute peripheral vestibulopathy", "Vestibulopathy, Acute Peripheral", "Peripheral Vestibulopathy, Acute", "VESTIBULOPATHY, ACUTE PERIPHERAL", "Acute Peripheral Vestibulopathies", "vestibular neuronitis (diagnosis)", "Vestibulopathies, Acute Peripheral", "Peripheral Vestibulopathies, Acute", "Vestibular neuronitis, unspecified ear", "Chlamydial infections epidemic vertigo", "acute peripheral vestibulopathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vestibular neuronitis", "shortest_name_length": 16}
{"curie": "UMLS:C5399819", "names": ["urinary tuberculosis", "Urinary tuberculosis", "TB - Urinary tuberculosis", "urinary tract tuberculosis", "tuberculosis urinary tract", "Tuberculosis, urinary tract", "Tuberculosis of urinary tract", "Tuberculosis of Urinary Organ", "Tuberculosis of Urinary Organs", "Tuberculosis of urinary organs", "tuberculosis of urinary organs", "Tuberculosis of urinary organs (disorder)", "tuberculosis of urinary organs (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tuberculosis of urinary organs", "shortest_name_length": 20}
{"curie": "UMLS:C3160834", "names": ["Thyroid cancer stage IV"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid cancer stage IV", "shortest_name_length": 23}
{"curie": "MONDO:0021179", "names": ["proteopathy", "Proteinopathy", "proteinopathy", "Proteinopathies", "proteopathic disease", "Proteostasis deficiency", "Protein folding disease", "Protein Folding Disease", "Proteostasis Deficiency", "disease, Protein folding", "Protein Folding Disorder", "Proteostasis dysfunction", "folding disease, Protein", "Protein Folding Diseases", "Folding Disease, Protein", "Protein folding diseases", "Proteostasis Dysfunction", "Deficiency, Proteostasis", "deficiency, Proteostasis", "Protein folding disorder", "Disease, Protein Folding", "folding diseases, Protein", "dysfunction, Proteostasis", "Proteostasis Deficiencies", "Protein Folding Disorders", "Disorder, Protein Folding", "proteostasis deficiencies", "Proteostasis dysfunctions", "Protein folding disorders", "Folding Disorder, Protein", "diseases, Protein folding", "disorder, Protein folding", "Dysfunction, Proteostasis", "folding disorder, Protein", "Proteostasis Dysfunctions", "disorders, Protein folding", "folding disorders, Protein", "Protein Misfolding Disease", "Protein Misfolding disease", "dysfunctions, Proteostasis", "deficiencies, Proteostasis", "Protein Misfolding diseases", "Misfolding Disease, Protein", "disease, Protein Misfolding", "Protein Misfolding disorder", "Protein Misfolding Diseases", "Disease, Protein Misfolding", "Protein Misfolding Disorder", "Misfolding disease, Protein", "disorder, Protein Misfolding", "Misfolding diseases, Protein", "Misfolding disorder, Protein", "Protein Misfolding disorders", "Disorder, Protein Misfolding", "Misfolding Disorder, Protein", "diseases, Protein Misfolding", "Protein Misfolding Disorders", "Misfolding disorders, Protein", "disorders, Protein Misfolding"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "proteostasis deficiencies", "shortest_name_length": 11}
{"curie": "MONDO:0017421", "names": ["terminal meromelia", "terminal limb defects", "isolated terminal limb defects", "nonsyndromic terminal limb defects", "non-syndromic terminal limb defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-syndromic terminal limb defects", "shortest_name_length": 18}
{"curie": "UMLS:C3274521", "names": ["Surfactant Protein D Deficiency", "Surfactant Apoprotein D Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Surfactant Protein D Deficiency", "shortest_name_length": 31}
{"curie": "UMLS:C0280281", "names": ["cancer of the renal pelvis and ureter, regional", "Regional Upper Urinary Tract Urothelial Carcinoma", "carcinoma of the renal pelvis and ureter, regional", "Regional Renal Pelvis and Ureter Urothelial Carcinoma", "Renal pelvis and ureter transitional cell cancer regional", "Regional Urothelial Cancer of the Renal Pelvis and Ureter", "Renal pelvis and ureteral cancer transitional cell regional", "Renal pelvis and ureteric cancer regional transitional cell", "Regional Urothelial Carcinoma of the Renal Pelvis and Ureter", "Regional Transitional Cell Cancer of Renal Pelvis and Ureter", "Regional Transitional Cell Carcinoma of Renal Pelvis and Ureter", "Transitional cell cancer of the renal pelvis and ureter regional", "regional transitional cell cancer of the renal pelvis and ureter", "Regional Transitional Cell Cancer of the Renal Pelvis and Ureter", "transitional cell cancer of the renal pelvis and ureter, regional"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Regional Urothelial Carcinoma of the Renal Pelvis and Ureter", "shortest_name_length": 47}
{"curie": "UMLS:C4524718", "names": ["Clinical Stage IVA Gastroesophageal Junction Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage IVA Gastroesophageal Junction Adenocarcinoma AJCC v8", "shortest_name_length": 67}
{"curie": "MONDO:0001882", "names": ["bacilluria", "Bacilluria", "bacteriuria", "Bacteriuria", "BACTERIURIA", "Bacteriurias", "Bacteriuria NOS", "Bacteria in urine", "High urine bacteria", "Bacteriuria (finding)", "bacteriuria (disease)", "Urine bacteria test positive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bacteriuria", "shortest_name_length": 10}
{"curie": "MONDO:0010386", "names": ["IPD2", "IMD33", "IPD2, FORMERLY", "IMMUNODEFICIENCY 33", "immunodeficiency 33", "immunodeficiency, Pure", "Immunodeficiency, pure", "immunodeficiency type 33", "NEMO deficiency syndrome", "Immunodeficiency, isolated", "immunodeficiency, isolated", "X-linked MSMD due to NEMO deficiency", "X-linked MSMD due to IKBKG deficiency", "immunodeficiency 33, X-linked recessive", "NF-kappa B essential modulator deficiency", "familial X-linked 1 atypical mycobacteriosis", "immunodeficiency 33, Mycobacteriosis, X-linked", "atypical Mycobacteriosis, familial, X-linked 1", "invasive pneumococcal disease, recurrent isolated, 2", "IKBKG invasive pneumococcal disease, recurrent isolated", "Immunodeficiency without anhidrotic ectodermal dysplasia", "immunodeficiency without anhidrotic ectodermal dysplasia", "[OBSOLETE] Atypical Mycobacteriosis, Familial, X-Linked 1", "invasive pneumococcal disease, recurrent isolated, type 2", "INVASIVE PNEUMOCOCCAL DISEASE, RECURRENT ISOLATED, 2, FORMERLY", "invasive pneumococcal disease, recurrent isolated caused by mutation in IKBKG", "X-linked mendelian susceptibility to mycobacterial diseases due to NEMO deficiency", "X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 33", "shortest_name_length": 4}
{"curie": "UMLS:C1335926", "names": ["Schistosoma Hematobium-Related Bladder Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Schistosoma Hematobium-Related Bladder Squamous Cell Carcinoma", "shortest_name_length": 62}
{"curie": "MONDO:0022471", "names": ["childhood aortic valve stenosis", "aortic valves stenosis of the child"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood aortic valve stenosis", "shortest_name_length": 31}
{"curie": "UMLS:C3899664", "names": ["Esophageal Cancer", "Childhood Esophageal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Esophageal Carcinoma", "shortest_name_length": 17}
{"curie": "UMLS:C2981393", "names": ["Stage IVC Appendix Cancer", "Stage IVC Appendix Carcinoma", "Stage IVC Appendix Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Appendix Carcinoma AJCC v7", "shortest_name_length": 25}
{"curie": "MONDO:0032941", "names": ["MYP27", "myopia 27", "MYOPIA 27", "MYOPIA 27, AUTOSOMAL DOMINANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopia 27", "shortest_name_length": 5}
{"curie": "UMLS:C3273103", "names": ["Gallbladder Cribriform Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gallbladder Cribriform Carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0021078", "names": ["Glandular papilloma", "Glandular Papilloma", "glandular papilloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glandular papilloma", "shortest_name_length": 19}
{"curie": "UMLS:C5230517", "names": ["BSNS", "Biphenotypic Sinonasal Sarcoma", "Biphenotypic sinonasal sarcoma", "Biphenotypic sinonasal sarcoma (morphologic abnormality)", "Low-Grade Sinonasal Sarcoma with Neural and Myogenic Differentiation", "Low Grade Sinonasal Sarcoma with Neural and Myogenic Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Biphenotypic sinonasal sarcoma", "shortest_name_length": 4}
{"curie": "UMLS:C4763647", "names": ["Relapsed Polymorphic Post-Transplant Lymphoproliferative Disorder", "Recurrent Polymorphic Post-Transplant Lymphoproliferative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Polymorphic Post-Transplant Lymphoproliferative Disorder", "shortest_name_length": 65}
{"curie": "MONDO:0018812", "names": ["MSH3-related AFAP", "MSH3-related attenuated FAP", "MSH3-related attenuated familial polyposis coli", "MSH3-related attenuated familial adenomatous polyposis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MSH3-related attenuated familial adenomatous polyposis", "shortest_name_length": 17}
{"curie": "UMLS:C1332353", "names": ["ASAP", "Prostatic Atypical Small Acinar Proliferation", "Atypical small acinar proliferation of prostate", "atypical small acinar proliferation of the prostate", "Atypical Small Acinar Proliferation of the Prostate Gland", "Atypical small acinar proliferation of prostate (disorder)", "Atypical small acinar proliferation of prostate (diagnosis)", "prostate gland carcinoma in situ atypical small acinar proliferation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypical Small Acinar Proliferation of the Prostate Gland", "shortest_name_length": 4}
{"curie": "MONDO:0008420", "names": ["senile wart", "Senile wart", "wart; senile", "senile; wart", "Senile warts", "senile warts", "old age; wart", "Wart(s);senile", "wart; senility", "senility; wart", "seborrheic wart", "Seborrheic wart", "senile; verruca", "verruca; senile", "seborrheic warts", "seborrhoeic wart", "seborrheic; wart", "senile keratosis", "Senile keratosis", "Seborrhoeic wart", "wart; seborrheic", "seborrhoeic warts", "Keratosis senilis", "keratosis senilis", "Seborrheic verruca", "Verruca seborrheica", "Seborrhoeic verruca", "Basal cell papilloma", "Seborrheic Keratoses", "seborrheic keratoses", "seborrheic keratosis", "Seborrheic keratosis", "seborrhea; keratosis", "Seborrheic Keratosis", "keratosis seborrheic", "Basal Cell Papilloma", "SEBORRHEIC KERATOSIS", "keratoses seborrheic", "Verruca seborrhoeica", "verruca; seborrheica", "seborrheica; verruca", "basal cell papilloma", "KERATOSIS SEBORRHEIC", "Keratosis Seborrheica", "Senile hyperkeratosis", "keratosis; seborrheic", "keratosis Seborrheica", "seborrhoeic keratosis", "KERATOSIS, SEBORRHEIC", "Keratosis seborrheica", "Keratosis, Seborrheic", "hyperkeratosis senile", "keratosis, seborrheic", "Keratoses, Seborrheic", "Seborrhoeic keratosis", "seborrheic; keratosis", "keratosis seborrheica", "Keratosis, seborrheic", "Basosquamous papilloma", "Keratosis seborrhoeica", "Seborrheic keratosis NOS", "BCP - Basal cell papilloma", "inverted follicular keratosis", "keratosis, seborrheic, somatic", "Pigmented basal cell papilloma", "Seborrheic keratosis (disorder)", "seborrheic keratosis (diagnosis)", "Senile hyperkeratosis (disorder)", "Senile hyperkeratosis (diagnosis)", "Seborrheic keratosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "seborrheic keratosis", "shortest_name_length": 11}
{"curie": "MONDO:0008173", "names": ["PC1", "pachyonychia congenita 1", "PACHYONYCHIA CONGENITA 1", "KRT16 pachyonychia congenita", "Type 1 Pachyonychia Congenita", "Pachyonychia Congenita Type 1", "pachyonychia congenita type 1", "Jadassohn-Lewandowsky Syndrome", "Pachyonychia Congenita, Type 1", "Jadassohn Lewandowsky Syndrome", "Jadassohn-Lewandowsky syndrome", "Pachyonychia Congenita Tarda, Type 1", "Jadassohn Lewandowski Syndrome (Pc 1)", "Jadassohn-Lewandowski Syndrome (Pc-1)", "Syndrome, Jadassohn-Lewandowski (Pc-1)", "JADASSOHN-LEWANDOWSKY SYNDROME, FORMERLY", "Jadassohn-Lewandowsky syndrome, formerly", "pachyonychia congenita caused by mutation in KRT16", "Pachyonychia Congenita, Jadassohn Lewandowsky Type", "Pachyonychia Congenita, Jadassohn-Lewandowsky Type", "pachyonychia congenita, Jadassohn-Lewandowsky type", "PACHYONYCHIA CONGENITA, JADASSOHN-LEWANDOWSKY TYPE, FORMERLY", "pachyonychia congenita, Jadassohn-Lewandowsky type, formerly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pachyonychia congenita 1", "shortest_name_length": 3}
{"curie": "MONDO:0005947", "names": ["Pneumorickettsiosis", "Rickettsial pneumonia", "Rickettsial Pneumonia", "rickettsial pneumonia", "Pneumonia, Rickettsial", "Rickettsial Pneumonias", "Pneumonias, Rickettsial", "Rickettsiaceae pneumonia", "Rickettsiaceae caused pneumonia", "Rickettsial pneumonia (disorder)", "bacterial pneumonia, rickettsial", "Rickettsial pneumonia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rickettsial pneumonia", "shortest_name_length": 19}
{"curie": "UMLS:C0339932", "names": ["Acute Moraxella catarrhalis bronchitis", "Acute Neisseria catarrhalis bronchitis", "bronchitis acute bacterial moraxella catarrhalis", "Acute Moraxella catarrhalis bronchitis (disorder)", "Acute Moraxella catarrhalis bronchitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Moraxella catarrhalis bronchitis", "shortest_name_length": 38}
{"curie": "MONDO:0009696", "names": ["JME", "EJM", "EJM1", "Janz syndrome", "JANZ SYNDROME", "Janz Syndrome", "janz syndrome", "Petit Mal, Impulsive", "petit mal, impulsive", "impulsive; petit mal", "PETIT MAL, IMPULSIVE", "Janz Impulsive Petit Mal", "Impulsive Petit Mal, Janz", "Petit Mal, Impulsive, Janz", "juvenile myoclonus epilepsy", "Impulsive petit mal of Janz", "Myoclonic Juvenile Epilepsy", "juvenile myoclonic epilepsy", "Juvenile myoclonus epilepsy", "Juvenile Myoclonic Epilepsy", "Juvenile myoclonic epilepsy", "epilepsy juvenile myoclonic", "Myoclonic Epilepsy, Juvenile", "Impulsive Petit Mal Epilepsy", "Juvenile Epilepsy, Myoclonic", "Epilepsy, Juvenile Myoclonic", "Impulsive petit-mal epilepsy", "epilepsy, myoclonic juvenile", "Epilepsy, Myoclonic Juvenile", "MYOCLONIC EPILEPSY, JUVENILE", "myoclonic epilepsy, juvenile", "EPILEPSY, MYOCLONIC JUVENILE", "Epilepsy, Myoclonic, Juvenile", "Adolescent Myoclonic Epilepsy", "Epilepsy, Adolescent Myoclonic", "myoclonic; epileptic, juvenile", "Myoclonic Epilepsy, Adolescent", "myoclonic epilepsy, juvenile, 1", "Myoclonic Epilepsy, Juvenile, 1", "Janz Juvenile Myoclonic Epilepsy", "JME - Juvenile myoclonic epilepsy", "JME (Juvenile Myoclonic Epilepsy)", "Myoclonic epilepsy of adolescence", "JMEs (Juvenile Myoclonic Epilepsy)", "Juvenile myoclonic epilepsy of Janz", "Juvenile Myoclonic Epilepsy of Janz", "Juvenile myoclonic epilepsy (disorder)", "juvenile myoclonic epilepsy (diagnosis)", "MYOCLONIC EPILEPSY, JUVENILE, SUSCEPTIBILITY TO, 1", "myoclonic epilepsy, juvenile, susceptibility to, 1", "generalized convulsive myoclonic seizure, juvenile"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile myoclonic epilepsy", "shortest_name_length": 3}
{"curie": "MONDO:0005854", "names": ["MCTD", "mctd", "MCTD SYNDROME", "Sharp syndrome", "sharp syndrome", "Sharp Syndrome", "Syndrome, Sharp", "Sharp's syndrome", "mix connective tissue disease", "connective mixed tissue disease", "connective disease mixed tissue", "collagen disease mixed vascular", "Mixed connective tissue disease", "Mixed Connective Tissue Disease", "mixed collagen vascular disease", "MIXED CONNECTIVE TISSUE DISEASE", "connective tissue disease mixed", "mixed connective tissue disease", "CONNECTIVE TISSUE DISEASE MIXED", "Mixed collagen vascular disease", "Connective Tissue Disease, Mixed", "disease; mixed connective tissue", "mixed, connective tissue; disorder", "Mixed collagen vascular disease, NOS", "Mixed connective tissue disease, NOS", "Connective tissue disease, mixed form", "MCTD - Mixed connective tissue disease", "connective tissue disease overlap syndrome", "Mixed collagen vascular disease (disorder)", "Connective tissue disease overlap syndrome", "mixed connective tissue disease (diagnosis)", "disease (or disorder); mixed connective tissue", "disease (or disorder); mixed, connective tissue", "Connective tissue disease overlap syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed connective tissue disease", "shortest_name_length": 4}
{"curie": "MONDO:0016818", "names": ["Mikati-Najjar-Sahli syndrome", "microcephaly-hypergonadotropic hypogonadism-short stature syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mikati-Najjar-Sahli syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0001139", "names": ["Masochism", "masochism", "Masochisms", "Masochism, NOS", "sexual masochism", "Sexual masochism", "Sexual Masochism", "Sexual Masochisms", "Masochism, Sexual", "Masochisms, Sexual", "Masochistic behavior", "Masochistic behaviour", "sexual masochism disorder", "Sexual masochism disorder", "Sexual masochism (disorder)", "Masochistic behavior (finding)", "sexual masochism disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sexual masochism disorder", "shortest_name_length": 9}
{"curie": "MONDO:0020177", "names": ["pigmented eyelid tumor", "pigmented palpebral tumor", "pigmented palpebral neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pigmented palpebral tumor", "shortest_name_length": 22}
{"curie": "MONDO:0042495", "names": ["ARTERIOSCLEROSIS RETINAL", "Arteriosclerosis retinal", "retinal arteriosclerosis", "retina; arteriosclerosis", "arteriosclerosis, retina", "Retinal arteriosclerosis", "ARTERIOSCLEROTIC RETINOPATHY", "Arteriosclerotic retinopathy", "arteriosclerotic retinopathy", "retinopathy, arteriosclerotic", "retina arteriosclerosis disorder", "arteriosclerosis disorder of retina", "Arteriosclerotic retinopathy (disorder)", "arteriosclerotic retinopathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arteriosclerotic retinopathy", "shortest_name_length": 24}
{"curie": "MONDO:0018125", "names": ["focal epilepsy-intellectual disability-dysarthria-ataxia syndrome", "focal epilepsy-intellectual disability-cerebro-cerebellar malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal epilepsy-intellectual disability-cerebro-cerebellar malformation", "shortest_name_length": 65}
{"curie": "UMLS:C4725706", "names": ["GLPD", "HHV8-positive germinotropic lymphoproliferative disorder", "HHV8-Positive Germinotropic Lymphoproliferative Disorder", "Germinotropic lymphoproliferative disorder caused by Human herpesvirus 8", "Germinotropic lymphoproliferative disorder caused by Human herpesvirus 8 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Germinotropic lymphoproliferative disorder caused by Human herpesvirus 8", "shortest_name_length": 4}
{"curie": "MONDO:0016974", "names": ["type B thymoma", "thymoma type B", "Thymoma Type B", "Thymoma type B", "plump cell thymoma", "Plump Cell Thymoma", "epithelioid thymoma", "epithelioid Thymoma", "Epithelioid Thymoma", "dendritic cell thymoma", "Dendritic cell thymoma", "Dendritic Cell Thymoma", "Thymoma type B (disorder)", "dendritic cell thymoma (disease)", "primary thymic epithelial tumor type B", "Primary thymic epithelial tumor type B", "Primary thymic epithelial neoplasm type B", "primary thymic epithelial neoplasm type B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thymoma type B", "shortest_name_length": 14}
{"curie": "MONDO:0001779", "names": ["vagina squamous papilloma", "vaginal squamous papilloma", "Vaginal Squamous Papilloma", "squamous papilloma of vagina", "Squamous Papilloma of Vagina", "Vaginal Squamous Cell Papilloma", "squamous papilloma of the vagina", "Squamous Papilloma of the Vagina"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vaginal squamous papilloma", "shortest_name_length": 25}
{"curie": "UMLS:C4520753", "names": ["Stage III Sinonasal Cancer AJCC v6 and v7", "Stage III Sinonasal Carcinoma AJCC v6 and v7", "Stage III Nasal Cavity and Paranasal Sinus Cancer", "Stage III Nasal Cavity and Paranasal Sinus Cancer AJCC v7", "Stage III Nasal Cavity and Paranasal Sinus Cancer AJCC v6", "Stage III Nasal Cavity and Paranasal Sinus Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Nasal Cavity and Paranasal Sinus Cancer AJCC v6 and v7", "shortest_name_length": 41}
{"curie": "MONDO:0007046", "names": ["hereditary papulotranslucent acrokeratoderma", "Acrokeratoderma, Hereditary Papulotranslucent", "ACROKERATODERMA, HEREDITARY PAPULOTRANSLUCENT", "acrokeratoderma, hereditary papulotranslucent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary papulotranslucent acrokeratoderma", "shortest_name_length": 44}
{"curie": "UMLS:C2986677", "names": ["stage I childhood non-Hodgkin lymphoma", "Stage I Childhood Non-Hodgkin Lymphoma", "Ann Arbor Stage I Childhood Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage I Childhood Non-Hodgkin Lymphoma", "shortest_name_length": 38}
{"curie": "MONDO:0014486", "names": ["MRD30", "autosomal dominant mental retardation 30", "mental retardation, autosomal dominant 30", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 30", "autosomal dominant intellectual disability 30", "intellectual disability, autosomal dominant 30", "mental retardation, autosomal dominant type 30", "intellectual disability, autosomal dominant type 30", "autosomal dominant intellectual developmental disorder 30", "autosomal dominant non-syndromic intellectual disability 30", "ZMYND11 intellectual disability-expressive aphasia-facial dysmorphism syndrome", "intellectual disability-expressive aphasia-facial dysmorphism syndrome caused by mutation in ZMYND11", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 30, WITH SPEECH DELAY AND BEHAVIORAL ABNORMALITIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 30", "shortest_name_length": 5}
{"curie": "MONDO:0043320", "names": ["Pseudosciatica", "wallet sciatica", "syndrome piriformis", "piriformis syndrome", "pyriformis syndrome", "Piriformis syndrome", "Piriformis Syndrome", "syndrome, Piriformis", "piriformis syndromes", "syndrome, piriformis", "Piriformis syndromes", "syndromes, Piriformis", "hip socket neuropathy", "syndromes, piriformis", "deep gluteal syndrome", "pelvic outlet syndrome", "Pelvic outlet syndrome", "piriformis muscle syndrome", "Piriformis Muscle Syndrome", "Muscle Syndrome, Piriformis", "piriformis muscle syndromes", "muscle syndrome, piriformis", "Syndrome, Piriformis Muscle", "Piriformis Muscle Syndromes", "syndrome, piriformis muscle", "Muscle Syndromes, Piriformis", "syndromes, piriformis muscle", "muscle syndromes, piriformis", "Syndromes, Piriformis Muscle", "Piriformis syndrome (disorder)", "piriformis syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "piriformis syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0021673", "names": ["post-bacterial disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "post-bacterial disorder", "shortest_name_length": 23}
{"curie": "UMLS:C1266117", "names": ["Proliferative Dermal Lesion in Congenital Nevus", "Proliferative dermal lesion in congenital nevus", "Proliferative dermal lesion in congenital naevus", "Proliferative Nodules in Congenital Melanocytic Nevus", "Proliferative dermal lesion in congenital nevus (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Proliferative dermal lesion in congenital nevus", "shortest_name_length": 47}
{"curie": "MONDO:0003510", "names": ["Testicular Cancer", "testicular cancer", "Testicular germ cell cancer", "testicular germ cell cancer", "Testicular Germ Cell Cancer", "Testicular germ cell cancer NOS", "Testicular ca. (no germ/tropho.)", "testicular ca. (no germ/tropho.)", "Malignant germ cell tumor of testis", "malignant germ cell tumor of testis", "Malignant Germ Cell Tumor of Testis", "malignant testicular germ cell tumor", "Malignant germ cell tumour of testis", "Malignant Testicular Germ Cell Tumor", "testicular malignant germ cell cancer", "malignant germ cell neoplasm of testis", "Malignant Germ Cell Neoplasm of Testis", "Malignant Testicular Germ Cell Neoplasm", "Malignant Germ Cell Tumor of the Testis", "malignant germ cell tumor of the testis", "malignant testicular germ cell neoplasm", "Testicular malignant germ cell tumor NOS", "Malignant Germ Cell Neoplasm of the Testis", "malignant germ cell neoplasm of the testis", "Malignant germ cell tumor of testis (disorder)", "testicular cancer (excluding germ cell or trophoblastic cancer)", "Testicular cancer (excluding germ cell or trophoblastic cancer)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant testicular germ cell tumor", "shortest_name_length": 17}
{"curie": "MONDO:0013043", "names": ["AHUS5", "aHUS with C3 anomaly", "D-HUS with C3 anomaly", "AHUS, SUSCEPTIBILITY TO, 5", "Ahus, susceptibility to, 5", "atypical HUS with C3 anomaly", "atypical hemolytic-uremic syndrome with C3 anomaly", "susceptibility to atypical hemolytic uremic syndrome 5", "HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 5", "hemolytic uremic syndrome, atypical, susceptibility to, 5", "hemolytic-uremic syndrome without diarrhea with C3 anomaly", "hemolytic uremic syndrome, atypical, susceptibility to, type 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical hemolytic-uremic syndrome with C3 anomaly", "shortest_name_length": 5}
{"curie": "MONDO:0000229", "names": ["Indian tick typhus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Indian tick typhus", "shortest_name_length": 18}
{"curie": "MONDO:0015535", "names": ["Diffuse xanthoma", "Xanthoma, diffuse", "Xanthoma multiplex", "Montgomery syndrome", "xanthoma disseminatum", "Xanthoma disseminatum", "Disseminated xanthoma", "Xanthoma Disseminatum", "Disseminatum, Xanthoma", "disseminatum; xanthoma", "xanthoma; disseminatum", "Xanthoma disseminatum (disorder)", "Disseminated xanthosiderohistiocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "xanthoma disseminatum", "shortest_name_length": 16}
{"curie": "MONDO:0019131", "names": ["ossification anomalies-psychomotor developmental delay syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ossification anomalies-psychomotor developmental delay syndrome", "shortest_name_length": 63}
{"curie": "UMLS:C4721452", "names": ["Intestinal T-cell lymphoma", "Intestinal T-Cell Lymphoma", "intestinal T-cell lymphoma", "Intestinal T-cell lymphomas", "Intestinal T-cell lymphoma NOS", "intestinal T-cell lymphoma (diagnosis)", "Intestinal T-cell lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal T-Cell Lymphoma", "shortest_name_length": 26}
{"curie": "UMLS:C3178892", "names": ["Pelvic Floor Disease", "Pelvic Floor Diseases", "Disease, Pelvic Floor", "Pelvic Floor Disorder", "Pelvic Floor Disorders", "Disorder, Pelvic Floor", "Diseases, Pelvic Floor", "Disorders, Pelvic Floor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pelvic Floor Disorders", "shortest_name_length": 20}
{"curie": "UMLS:C4331478", "names": ["Unresectable Thyroid Gland Cancer", "Unresectable Thyroid Gland Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Thyroid Gland Carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0011195", "names": ["USH1E", "Usher syndrome type 1E", "Usher syndrome type IE", "USHER syndrome, type IE", "Usher syndrome, type 1E", "USHER SYNDROME, TYPE IE", "Usher Syndrome, Type IE", "USHER SYNDROME, TYPE IE (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Usher syndrome type 1E", "shortest_name_length": 5}
{"curie": "UMLS:C0858516", "names": ["Subacute combined cord degeneration", "SACD (sub-acute combined degeneration of cord)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subacute combined cord degeneration", "shortest_name_length": 35}
{"curie": "MONDO:0008381", "names": ["dominant pericentral pigmentary retinopathy", "RETINOPATHY, PERICENTRAL PIGMENTARY, DOMINANT", "Retinopathy, Pericentral Pigmentary, Dominant", "retinopathy, pericentral pigmentary, dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dominant pericentral pigmentary retinopathy", "shortest_name_length": 43}
{"curie": "MONDO:0016503", "names": ["CEVD", "congenital erosive and vesicular dermatosis", "congenital erosive and vesicular dermatosis with reticulated supple scarring"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital erosive and vesicular dermatosis", "shortest_name_length": 4}
{"curie": "UMLS:C0546136", "names": ["Neurotoxicity due to methotrexate", "Neurotoxicity caused by methotrexate", "Neurotoxicity caused by methotrexate (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neurotoxicity due to methotrexate", "shortest_name_length": 33}
{"curie": "MONDO:0011943", "names": ["SLEN2", "SYSTEMIC LUPUS ERYTHEMATOSUS WITH NEPHRITIS, SUSCEPTIBILITY TO, 2", "systemic lupus erythematosus with nephritis, susceptibility to, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "systemic lupus erythematosus with nephritis, susceptibility to, 2", "shortest_name_length": 5}
{"curie": "MONDO:0013135", "names": ["Fhl5", "HLH5", "FHL5", "HPLH5", "familial hemophagocytic lymphohistiocytosis 5", "Hemophagocytic Lymphohistiocytosis, Familial, 5", "HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 5", "hemophagocytic lymphohistiocytosis, familial, 5", "STXBP2 genetic hemophagocytic lymphohistiocytosis", "familial hemophagocytic lymphohistiocytosis type 5", "hemophagocytic lymphohistiocytosis, familial, type 5", "genetic hemophagocytic lymphohistiocytosis caused by mutation in STXBP2", "hemophagocytic lymphohistiocytosis, familial, 5, with or without microvillus inclusion disease", "HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 5, WITH OR WITHOUT MICROVILLUS INCLUSION DISEASE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial hemophagocytic lymphohistiocytosis 5", "shortest_name_length": 4}
{"curie": "MONDO:0005946", "names": ["Rhinosporosis", "rhinosporidiosis", "RHINOSPORIDIOSIS", "Rhinosporidiosis", "Rhinosporidioses", "Rhinosporidiosis (disorder)", "rhinosporidiosis (diagnosis)", "Rhinosporidium seeberi Infection", "Rhinosporidium seeberi Infections", "Rhinosporidium seeberi; infection", "Infection, Rhinosporidium seeberi", "infection; Rhinosporidium seeberi", "Infection by Rhinosporidium seeberi", "infection by Rhinosporidium seeberi", "Rhinosporidium seeberi infectious disease", "Rhinosporidium seeberi disease or disorder", "Rhinosporidium seeberi caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rhinosporidiosis", "shortest_name_length": 13}
{"curie": "UMLS:C3274592", "names": ["Lipofibromatosis", "Infantile Fibromatosis, Non-Desmoid Type", "Lipofibromatosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lipofibromatosis", "shortest_name_length": 16}
{"curie": "MONDO:0000934", "names": ["larynx leiomyoma", "Larynx Leiomyoma", "leiomyoma of larynx", "Laryngeal Leiomyoma", "laryngeal leiomyoma", "Leiomyoma of Larynx", "leiomyoma of the larynx", "Leiomyoma of the Larynx"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laryngeal leiomyoma", "shortest_name_length": 16}
{"curie": "UMLS:C1706699", "names": ["Acoustic shock", "Acoustic Shock"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acoustic shock", "shortest_name_length": 14}
{"curie": "UMLS:C4744476", "names": ["Thyroid Gland Black Follicular Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Black Follicular Adenoma", "shortest_name_length": 38}
{"curie": "MONDO:0006672", "names": ["balanitis", "Balanitis", "Penisitis", "BALANITIS", "Balanitides", "Balanitis NOS", "Penis inflamed", "Penis inflammation", "inflammation penis", "Inflammation;penis", "penis inflammation", "PENIS INFLAMMATION", "PENILE INFLAMMATION", "inflammation; penis", "penile inflammation", "penis; inflammation", "Balanitis (disorder)", "balanitis (diagnosis)", "Inflammation of penis", "INFLAMMATION OF PENIS", "inflammation of penis", "glans penis inflammation", "inflammation of the penis", "inflammation of glans penis", "Inflammatory disorder of penis", "inflammatory disorders of penis", "Inflammatory disorder of penis (disorder)", "disease (or disorder); penis, inflammatory", "inflammatory disorders of penis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "balanitis", "shortest_name_length": 9}
{"curie": "UMLS:C2931853", "names": ["Speech disturbance - use of faulty phrasing and unrelated words"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Speech disturbance - use of faulty phrasing and unrelated words", "shortest_name_length": 63}
{"curie": "MONDO:0006476", "names": ["gallbladder cancer, anaplastic", "Anaplastic Gallbladder Carcinoma", "anaplastic gallbladder carcinoma", "Anaplastic Carcinoma of Gallbladder", "anaplastic carcinoma of gallbladder", "undifferentiated gallbladder cancer", "Undifferentiated Gallbladder Cancer", "gallbladder cancer, undifferentiated", "Undifferentiated Gallbladder Carcinoma", "gallbladder undifferentiated carcinoma", "Gallbladder Undifferentiated Carcinoma", "undifferentiated gallbladder carcinoma", "gall bladder undifferentiated carcinoma", "anaplastic carcinoma of the gallbladder", "Anaplastic Carcinoma of the Gallbladder", "undifferentiated carcinoma of gallbladder", "Undifferentiated Carcinoma of Gallbladder", "Undifferentiated Carcinoma of the Gallbladder", "undifferentiated carcinoma of the gallbladder", "gallbladder, undifferentiated carcinoma of the", "anaplastic carcinoma of gallbladder (diagnosis)", "undifferentiated carcinoma of gallbladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "undifferentiated gallbladder carcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0024471", "names": ["non-inflammatory vasculopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-inflammatory vasculopathy", "shortest_name_length": 29}
{"curie": "UMLS:C4049181", "names": ["Enteropathic spondylitis", "Enteropathic Spondylitis", "Enteropathic Spondyloarthritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Enteropathic spondylitis", "shortest_name_length": 24}
{"curie": "MONDO:0014427", "names": ["CORD20", "cone-rod dystrophy 20", "CONE-ROD DYSTROPHY 20", "POC1B cone-rod dystrophy", "cone-rod dystrophy type 20", "cone-rod dystrophy caused by mutation in POC1B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cone-rod dystrophy 20", "shortest_name_length": 6}
{"curie": "UMLS:C4528590", "names": ["Stage IIIB Breast Cancer", "Prognostic Stage IIIB Breast Cancer AJCC v8", "Prognostic Stage IIIB Breast Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prognostic Stage IIIB Breast Cancer AJCC v8", "shortest_name_length": 24}
{"curie": "MONDO:0019574", "names": ["Secondary intestinal lymphangiectasis", "Secondary intestinal lymphangiectasia", "secondary intestinal lymphangiectasia", "Secondary intestinal lymphangiectasis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary intestinal lymphangiectasia", "shortest_name_length": 37}
{"curie": "UMLS:C5237318", "names": ["Bone Void"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone Void", "shortest_name_length": 9}
{"curie": "MONDO:0021012", "names": ["KAZA1", "kala-Azar, susceptibility to, 1", "KALA-AZAR, SUSCEPTIBILITY TO, 1", "susceptibility to visceral leishmaniasis, 1", "leishmaniasis, visceral, susceptibility to, 1", "LEISHMANIASIS, VISCERAL, SUSCEPTIBILITY TO, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "susceptibility to visceral leishmaniasis, 1", "shortest_name_length": 5}
{"curie": "MONDO:0009693", "names": ["Kahler", "Myeloma", "myeloma", "MYELOMA", "myelomas", "myelomatosis", "Myelomatosis", "Myeloma, NOS", "Plasmocytoma", "Myelomatoses", "KAHLER DISEASE", "kahler disease", "Kahler disease", "Al amyloidosis", "Kahler Disease", "Disease, Kahler", "Kahler's disease", "Myeloma-Multiple", "kahler's disease", "MULTIPLE MYELOMA", "multiple myeloma", "Myeloma;multiple", "Multiple myeloma", "Multiple Myeloma", "Myeloma Multiple", "myeloma, multiple", "Myeloma, Multiple", "Myeloma-Multiples", "MYELOMA, MULTIPLE", "Multiple Myelomas", "multiple myelomas", "Myelomas, Multiple", "myeloma - multiple", "myelomata; multiple", "plasma cell myeloma", "Plasma-cell myeloma", "Plasma-Cell Myeloma", "PLASMA CELL MYELOMA", "Plasma Cell Myeloma", "Plasmacytic myeloma", "Plasma cell myeloma", "Plasma-cell Myeloma", "Myeloma, Plasma-Cell", "Multiple myeloma NOS", "Plasma-Cell Myelomas", "Plasma cell myelomas", "Myeloma, Plasma Cell", "myeloma, plasma cell", "plasma cell neoplasm", "Plasma Cell Myelomas", "Plasma cell neoplasm", "Cell Myeloma, Plasma", "multiple myeloma (MM)", "plasma cell neoplasms", "Myelomas, Plasma-Cell", "MYELOMATOSIS MULTIPLE", "neoplasm, plasma cell", "amyloidosis, systemic", "Cell Myelomas, Plasma", "Myelomas, Plasma Cell", "Myelomatosis multiple", "multiple myelomatosis", "medullary plasmacytoma", "Medullary plasmacytoma", "KAHLER-BOZZOLO DISEASE", "Multiple myeloma (disorder)", "Multiple myeloma (clinical)", "multiple myeloma (diagnosis)", "plasma cell myeloid neoplasm", "MULTIPLE MYELOMA MYELOMATOSIS", "Peripheral plasma cell myeloma", "myeloma, plasma cell, malignant", "MYELOMA, PLASMA CELL, MALIGNANT", "myeloid neoplasm of plasma cell", "Multiple Myeloma/Plasma Cell Myeloma", "multiple myeloma/plasma cell myeloma", "Multiple myeloma / Plasma cell neoplasm", "Plasma cell myeloma (morphologic abnormality)", "multiple myeloma and other plasma cell neoplasms", "multiple myeloma, resistance to, Somatic mutation", "multiple myeloma, susceptibility to, Somatic mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "plasma cell myeloma", "shortest_name_length": 6}
{"curie": "MONDO:0032609", "names": ["MC1DN4", "nuclear type mitochondrial complex I deficiency 4", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 4", "mitochondrial complex 1 deficiency, nuclear type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 4", "shortest_name_length": 6}
{"curie": "UMLS:C5243563", "names": ["Hormone receptor positive breast cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hormone receptor positive breast cancer", "shortest_name_length": 39}
{"curie": "UMLS:C4526716", "names": ["Stage IA3 Lung Cancer", "Stage IA3 Lung Cancer AJCC v8", "stage IA3 lung cancer AJCC v8", "stage IA3 non-small cell lung cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA3 Lung Cancer AJCC v8", "shortest_name_length": 21}
{"curie": "MONDO:0008316", "names": ["THPH3", "Acquired protein C deficiency", "acquired protein C deficiency", "Protein C deficiency, acquired", "Protein C Deficiency, Acquired", "PROTEIN C DEFICIENCY, ACQUIRED", "autosomal dominant PROC deficiency", "PROC Deficiency, Autosomal Dominant", "PROC DEFICIENCY, AUTOSOMAL DOMINANT", "Proc deficiency, autosomal dominant", "autosomal dominant protein C deficiency", "PROTEIN C DEFICIENCY, AUTOSOMAL DOMINANT", "Acquired protein C deficiency (disorder)", "Protein C Deficiency, Autosomal Dominant", "protein C deficiency, autosomal dominant", "Protein C deficiency, autosomal dominant", "acquired protein C deficiency (diagnosis)", "protein C deficiency, autosomal dominant (diagnosis)", "autosomal dominant thrombophilia due to protein C deficiency", "thrombophilia due to protein C deficiency, autosomal dominant", "thrombophilia due to PROTEIN C deficiency, autosomal dominant", "THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL DOMINANT", "thrombophilia 3 due to protein C deficiency, autosomal dominant", "Thrombophilia, Hereditary, Due To Protein C Deficiency, Autosomal Dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombophilia due to protein C deficiency, autosomal dominant", "shortest_name_length": 5}
{"curie": "MONDO:0012439", "names": ["ALGS2", "Alagille Syndrome 2", "ALAGILLE SYNDROME 2", "Alagille syndrome 2", "Alagille syndrome type 2", "Alagille syndrome due to a NOTCH2 point mutation", "Arteriohepatic dysplasia due to a NOTCH2 point mutation", "Alagille-Watson syndrome due to a NOTCH2 point mutation", "Syndromic bile duct paucity due to a NOTCH2 point mutation", "syndromic bile duct paucity due to a NOTCH2 point mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alagille syndrome due to a NOTCH2 point mutation", "shortest_name_length": 5}
{"curie": "UMLS:C3640142", "names": ["Stage II Differentiated Thyroid Gland Cancer Under 45 Years", "Stage II Differentiated Thyroid Gland Carcinoma Under 45 Years", "Stage II Differentiated Thyroid Gland Carcinoma Under 45 Years AJCC v7", "Stage II Thyroid Gland Papillary or Follicular Carcinoma Under 45 Years"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Differentiated Thyroid Gland Carcinoma Under 45 Years AJCC v7", "shortest_name_length": 59}
{"curie": "MONDO:0015372", "names": ["autosomal dominant macrothrombocytopenia", "Autosomal dominant macrothrombocytopenia", "Autosomal dominant macrothrombocytopenia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant macrothrombocytopenia", "shortest_name_length": 40}
{"curie": "MONDO:0008406", "names": ["EDMD3", "autosomal recessive Emery-Dreifuss muscular dystrophy", "Emery-Dreifuss muscular dystrophy, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive Emery-Dreifuss muscular dystrophy", "shortest_name_length": 5}
{"curie": "UMLS:C2347756", "names": ["Advanced Favorable Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Favorable Hodgkin Lymphoma", "shortest_name_length": 35}
{"curie": "UMLS:C1334824", "names": ["Multiple Lung Hamartomas", "Multiple hamartoma of lung", "Multiple pulmonary hamartomas", "Multiple Pulmonary Hamartomas", "Multiple Chondromatous Lung Hamartoma", "Multiple hamartoma of lung (disorder)", "Multiple Chondromatous Hamartoma of Lung", "Multiple Chondromatous Hamartoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Multiple hamartoma of lung", "shortest_name_length": 24}
{"curie": "MONDO:0044326", "names": ["DEDSM", "DEVELOPMENTAL DELAY AND SEIZURES WITH OR WITHOUT MOVEMENT ABNORMALITIES", "developmental delay and seizures with or without movement abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental delay and seizures with or without movement abnormalities", "shortest_name_length": 5}
{"curie": "MONDO:0005186", "names": ["addiction cocaine", "cocaine addiction", "Cocaine Addiction", "Cocaine addiction", "cocaine dependence", "dependence cocaine", "Addiction, Cocaine", "COCAINE DEPENDENCY", "Cocaine dependence", "Cocaine Dependence", "Dependence, Cocaine", "cocaine; dependence", "dependence; cocaine", "Dependences, Cocaine", "Dependence on cocaine", "Addiction;drug(s);cocaine", "Cocaine dependence (disorder)", "cocaine dependence (diagnosis)", "Cocaine dependence, unspecified", "Cocaine dependence, unspecified use", "Mental and behavioral disorders due to use of cocaine, dependence syndrome", "Mental and behavioural disorders due to use of cocaine, dependence syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cocaine dependence", "shortest_name_length": 17}
{"curie": "UMLS:C3495442", "names": ["Phantom pain", "phantom pain", "Phantom Pain", "Phantom pain (disorder)", "phantom pain (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Phantom pain", "shortest_name_length": 12}
{"curie": "MONDO:0018185", "names": ["congenital anomaly of the great veins"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital anomaly of the great veins", "shortest_name_length": 37}
{"curie": "MONDO:0002744", "names": ["Fallopian Tube Mucinous Adenocarcinoma", "fallopian tube mucinous adenocarcinoma", "mucinous adenocarcinoma of fallopian tube", "mucinous adenocarcinoma of fallopian tube (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fallopian tube mucinous adenocarcinoma", "shortest_name_length": 38}
{"curie": "UMLS:C0279085", "names": ["Immunosuppressive Treatment Related Kaposi Sarcoma", "immunosuppressive treatment related Kaposi sarcoma", "Immunosuppressive Treatment Related Kaposi's Sarcoma", "Kaposi's sarcoma, immunosuppressive treatment related", "Kaposi Sarcoma Related to Immunosuppressive Treatment", "sarcoma, immunosuppressive treatment related Kaposi's", "sarcoma, Kaposi's, immunosuppressive treatment related", "Kaposi's Sarcoma Related to Immunosuppressive Treatment", "multiple hemorrhagic sarcoma, immunosuppressive treatment related", "sarcoma, multiple hemorrhagic, immunosuppressive treatment related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kaposi Sarcoma Related to Immunosuppressive Treatment", "shortest_name_length": 50}
{"curie": "MONDO:0044701", "names": ["CONDBA", "UBTF-related disorder", "NEURODEGENERATION, CHILDHOOD-ONSET, WITH BRAIN ATROPHY", "neurodegeneration, childhood-onset, with brain atrophy", "childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder", "shortest_name_length": 6}
{"curie": "MONDO:0001602", "names": ["Labia Minora Cancer", "Labia Minora cancer", "labia minora cancer", "labia minora carcinoma", "Labia Minora Carcinoma", "labium minora carcinoma", "Carcinoma of Labia Minora", "carcinoma of labia minora", "carcinoma of labium minora", "Carcinoma of the Labia Minora", "carcinoma of the labia minora"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "labia minora carcinoma", "shortest_name_length": 19}
{"curie": "MONDO:0005514", "names": ["Nanophthalmos", "nanophthalmia", "nanophthalmos", "Nanophthalmia", "Nanophthalmia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nanophthalmia", "shortest_name_length": 13}
{"curie": "UMLS:C0376185", "names": ["Renal tubular acidosis type 4", "type iv renal tubular acidosis", "type IV renal tubular acidosis", "Type IV renal tubular acidosis", "Renal tubular acidosis type IV", "Type IV Renal Tubular Acidosis", "RENAL TUBULAR ACIDOSIS TYPE IV", "renal tubular acidosis type iv", "Acidosis, Renal Tubular Type IV", "hyporeninemic hypoaldosteronism", "Hyporeninemic hypoaldosteronism", "Hyporeninemic Hypoaldosteronism", "Renal Tubular Acidosis, Type IV", "Hyporeninaemic hypoaldosteronism", "Hypoaldosteronism, Hyporeninemic", "Hyporeninenmic Hypoaldosteronism", "Hyperkalemic renal tubular acidosis", "Hyperkalaemic renal tubular acidosis", "type IV renal tubular acidosis (diagnosis)", "Hyporeninemic hypoaldosteronism (disorder)", "hyporeninemic hypoaldosteronism (diagnosis)", "RTA Type IV - Type IV renal tubular acidosis", "Hyperkalemic renal tubular acidosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypoaldosteronism, Hyporeninemic", "shortest_name_length": 29}
{"curie": "UMLS:C1112748", "names": ["Colon Tubulovillous Adenoma", "Colonic Tubulovillous Adenoma", "Colonic tubulovillous adenoma", "Tubulovillous Adenoma of Colon", "Tubulovillous Adenoma of the Colon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colonic tubulovillous adenoma", "shortest_name_length": 27}
{"curie": "MONDO:0001200", "names": ["Secondary hypertension", "Hypertension secondary", "HYPERTENSION SECONDARY", "Hypertension;secondary", "secondary hypertension", "hypertension secondary", "Secondary Hypertension", "hypertension; secondary", "secondary; hypertension", "Secondary hypertension NOS", "Secondary hypertension, NOS", "Secondary hypertensive syndrome", "Secondary hypertension (disorder)", "Unspecified secondary hypertension", "secondary hypertension (diagnosis)", "unspecified secondary hypertension", "Secondary hypertension, unspecified", "unspecified secondary hypertension (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary hypertension", "shortest_name_length": 22}
{"curie": "UMLS:C1262195", "names": ["Echoacousia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Echoacousia", "shortest_name_length": 11}
{"curie": "MONDO:0015023", "names": ["NEM11", "nemaline myopathy 11", "NEMALINE MYOPATHY 11", "MYPN-related myopathy", "MYPN nemaline myopathy", "nemaline myopathy type 11", "NEMALINE MYOPATHY 11, AUTOSOMAL RECESSIVE", "nemaline myopathy 11, autosomal recessive", "nemaline myopathy caused by mutation in MYPN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MYPN-related myopathy", "shortest_name_length": 5}
{"curie": "UMLS:C4744399", "names": ["Recurrent Uterine Corpus Carcinosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Uterine Corpus Carcinosarcoma", "shortest_name_length": 39}
{"curie": "UMLS:C4511590", "names": ["cannabis abuse with cannabis hyperemesis syndrome", "cannabis abuse with cannabis hyperemesis syndrome (diagnosis)", "Cannabis hyperemesis syndrome co-occurrent and due to cannabis abuse", "Cannabis hyperemesis syndrome co-occurrent and due to cannabis abuse (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cannabis hyperemesis syndrome co-occurrent and due to cannabis abuse", "shortest_name_length": 49}
{"curie": "MONDO:0008866", "names": ["Nose, Median cleft of", "median fissure of Nose", "autosomal recessive bifid nose", "bifid nose, autosomal recessive", "Bifid Nose, Autosomal Recessive", "BIFID NOSE, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bifid nose, autosomal recessive", "shortest_name_length": 21}
{"curie": "UMLS:C5668301", "names": ["Thymic Adenocarcinoma, NOS", "Thymic Adenocarcinoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thymic Adenocarcinoma, Not Otherwise Specified", "shortest_name_length": 26}
{"curie": "MONDO:0030266", "names": ["IMD80", "MCM10 DEFICIENCY", "MCM10 deficiency", "immunodeficiency 80 with or without cardiomyopathy", "immunodeficiency with or without congenital cardiomyopathy", "IMMUNODEFICIENCY 80 WITH OR WITHOUT CONGENITAL CARDIOMYOPATHY", "immunodeficiency 80 with or without congenital cardiomyopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 80 with or without congenital cardiomyopathy", "shortest_name_length": 5}
{"curie": "MONDO:0018249", "names": ["finger hyperphalangy - toe anomalies - severe pectus excavatum syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "finger hyperphalangy - toe anomalies - severe pectus excavatum syndrome", "shortest_name_length": 71}
{"curie": "UMLS:C1504421", "names": ["incompatibility rh", "rh incompatibility", "Rh Incompatibility", "Incompatibility, Rh", "Rh Incompatibilities", "Incompatibility (Rh)", "incompatibilities rh", "Rhesus incompatibility", "Rhesus Incompatibility", "rh factor incompatibility", "RH FACTOR INCOMPATIBILITY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rh Incompatibility", "shortest_name_length": 18}
{"curie": "MONDO:0010507", "names": ["Dup(X)(q25)", "Xq25 microtriplication", "Xq25 duplication syndrome", "Xq25 triplication syndrome", "Xq25 Microduplication Syndrome", "Xq25 microduplication syndrome", "CHROMOSOME Xq25 DUPLICATION SYNDROME", "CHROMOSOME Xq25 TRIPLICATION SYNDROME", "Xq25 microduplication syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Xq25 microduplication syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0001297", "names": ["heart tamponade", "HEART TAMPONADE", "Rose's tamponade", "HEART, TAMPONADE", "rose's tamponade", "cardiac tamponade", "TAMPONADE CARDIAC", "CARDIAC TAMPONADE", "Cardiac Tamponade", "Tamponade cardiac", "tamponade cardiac", "Cardiac tamponade", "tamponade; cardiac", "Cardiac Tamponades", "Tamponade, Cardiac", "Tamponades, Cardiac", "Pericardial Tamponade", "pericardial tamponade", "PERICARDIAL TAMPONADE", "Pericardial tamponade", "Pericardial Tamponades", "Tamponade, Pericardial", "Tamponades, Pericardial", "Cardiac tamponade (disorder)", "cardiac tamponade (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiac tamponade", "shortest_name_length": 15}
{"curie": "UMLS:C0263292", "names": ["Sun Exposure Dermatitis", "Unspecified dermatitis due to sun", "Contact dermatitis due to solar radiation, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unspecified dermatitis due to sun", "shortest_name_length": 23}
{"curie": "MONDO:0000320", "names": ["Glandular tularemia", "glandular tularemia", "lymph node tularemia", "Glandular tularaemia", "Glandular tularemia (disorder)", "glandular tularemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glandular tularemia", "shortest_name_length": 19}
{"curie": "MONDO:0008957", "names": ["Missing cervical vertebrae", "Cervical vertebral agenesis", "Cervical vertebrae agenesis", "Agenesis of cervical vertebra", "cervical vertebrae, agenesis of", "CERVICAL VERTEBRAE, AGENESIS OF", "Cervical Vertebrae, Agenesis Of", "Congenital absence of cervical vertebra", "Agenesis of cervical vertebra (disorder)", "Congenital absence of cervical vertebra (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical vertebrae, agenesis of", "shortest_name_length": 26}
{"curie": "MONDO:0017116", "names": ["congenital communicating hydrocephalus", "congenital non-obstructive hydrocephalus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital communicating hydrocephalus", "shortest_name_length": 38}
{"curie": "UMLS:C4330674", "names": ["Metastatic Germ Cell Tumor", "Metastatic Germ Cell Neoplasm", "Metastatic Malignant Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Malignant Germ Cell Tumor", "shortest_name_length": 26}
{"curie": "UMLS:C4520964", "names": ["Pancreatic Cancer Stage I", "stage I pancreatic cancer", "Stage I Pancreatic Cancer", "Stage I Pancreatic Carcinoma", "Stage I Carcinoma of Pancreas", "Stage I Pancreatic Cancer AJCC v7", "Stage I Carcinoma of the Pancreas", "Stage I Pancreatic Cancer AJCC v6", "Stage I Pancreatic Cancer AJCC v6 and v7", "Stage I Exocrine and Endocrine Pancreatic Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Pancreatic Cancer AJCC v6 and v7", "shortest_name_length": 25}
{"curie": "UMLS:C4553570", "names": ["Stage III Penile Cancer", "Stage III Penile Cancer AJCC v8", "Stage III Penile Squamous Cell Carcinoma AJCC v8", "Stage III Squamous Cell Carcinoma of the Penis AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Penile Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "MONDO:0016121", "names": ["congenital myotonia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myotonia", "shortest_name_length": 19}
{"curie": "MONDO:0016986", "names": ["Smooth muscle nevus", "Smooth muscle naevus", "Nevus of pilar muscle", "Naevus of pilar muscle", "Congenital erector pili hamartoma", "congenital smooth muscle hamartoma", "Congenital arrector pili hamartoma", "Congenital smooth muscle hamartoma", "Congenital erector pili hamartoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital smooth muscle hamartoma", "shortest_name_length": 19}
{"curie": "MONDO:0013627", "names": ["3M3", "3M syndrome 3", "3M SYNDROME 3", "3-M syndrome 3", "CCDC8 3-M syndrome", "THREE M SYNDROME 3", "three M syndrome 3", "three M syndrome type 3", "3-M syndrome caused by mutation in CCDC8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "3M syndrome 3", "shortest_name_length": 3}
{"curie": "UMLS:C4053516", "names": ["MBT/APMT", "Borderline Ovarian Mucinous Tumor/Atypical Proliferative Ovarian Mucinous Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Ovarian Mucinous Tumor/Atypical Proliferative Ovarian Mucinous Tumor", "shortest_name_length": 8}
{"curie": "MONDO:0009378", "names": ["Hyperalaninemia", "HYPERALANINEMIA", "hyperalaninemia", "Hyperalaninaemia", "hyper-B-alaninemia", "hyperbetaalaninemia", "HYPER-BETA-ALANINEMIA", "Hyper-Beta-Alaninemia", "Hyper-beta-alaninemia", "hyper-beta-alaninemia", "Hyper-beta-alaninaemia", "Increased serum alanine", "Increased blood alanine", "hyper-B-alaninemia (diagnosis)", "Hyper-beta-alaninemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyper-beta-alaninemia", "shortest_name_length": 15}
{"curie": "MONDO:0009339", "names": ["BASD2", "CBAS2", "congenital bile acid synthesis defect 2", "BILE ACID SYNTHESIS DEFECT, CONGENITAL, 2", "Bile acid synthesis defect, congenital, 2", "bile acid synthesis defect, congenital, 2", "congenital bile acid synthesis defect type 2", "AKR1D1 congenital bile acid synthesis defect", "Congenital bile acid synthesis defect type 2", "congenital bile acid synthesis defect, type 2", "bile acid synthesis defect, congenital, type 2", "Delta-4-3-oxosteroid-5-beta-reductase deficiency", "Congenital Bile Acid Synthesis Defect Type 2 (CBAS2)", "Delta-4-3-oxosteroid-5-beta-reductase deficiency (disorder)", "Cholestasis with delta(4)-3-oxosteroid 5-beta-reductase deficiency", "CHOLESTASIS WITH DELTA(4)-3-OXOSTEROID 5-BETA-REDUCTASE DEFICIENCY", "congenital bile acid synthesis defect caused by mutation in AKR1D1", "cholestasis with delta(4)-3-oxosteroid 5-beta-reductase deficiency", "cholestasis with Delta(4)-3-oxosteroid 5-Beta-reductase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital bile acid synthesis defect 2", "shortest_name_length": 5}
{"curie": "MONDO:0007576", "names": ["ESOPHAGUS CANCER", "Esophagus Cancer", "esophagus cancer", "oesophagus cancer", "Esophagus--Cancer", "Esophageal Cancer", "Esophagus Cancers", "ESOPHAGEAL CANCER", "esophageal cancer", "Cancer, Esophagus", "Esophageal cancer", "Cancer, Esophageal", "Cancers, Esophagus", "Oesophageal cancer", "oesophageal cancer", "Esophageal Cancers", "Cancer of esophagus", "Cancer of Esophagus", "Cancers, Esophageal", "cancer of esophagus", "Cancer of oesophagus", "cancer of oesophagus", "oesophageal neoplasm", "Esophageal cancer NOS", "Oesophageal cancer NOS", "Cancer of the Esophagus", "Escc, susceptibility to", "ESCC, SUSCEPTIBILITY TO", "cancer of the esophagus", "Ca upper third esophagus", "CA - Cancer of esophagus", "Ca lower third esophagus", "Neoplasm malig;oesophagus", "Malignant Esophagus Tumor", "CA - Cancer of oesophagus", "Ca upper third oesophagus", "Ca middle third esophagus", "malignant esophagus tumor", "Ca lower third oesophagus", "Malignant Esophageal Tumor", "esophageal cancer, somatic", "malignant esophageal tumor", "Esophageal malignant tumor", "Ca middle third oesophagus", "Malignant tumor of esophagus", "malignant esophagus neoplasm", "Malignant Tumor of Esophagus", "malignant tumor of esophagus", "esophageal carcinoma, somatic", "esophageal cancer (diagnosis)", "Malignant Esophageal Neoplasm", "malignant esophageal neoplasm", "Malignant tumour of oesophagus", "Esophageal neoplasms malignant", "malignant neoplasm of esophagus", "Malignant Neoplasm of Esophagus", "Oesophageal neoplasms malignant", "Malignant neoplasm of esophagus", "Malignant neoplasm of oesophagus", "Malignant Tumor of the Esophagus", "malignant tumor of the esophagus", "malignant neoplasm of the esophagus", "Malignant neoplasm of esophagus NOS", "Malignant Neoplasm of the Esophagus", "malignant neosplasm of the esophagus", "Malignant neoplasm of oesophagus NOS", "Malignant neoplasm of esophagus, NOS", "malignant neosplasm of the oesophagus", "Malignant neoplasm of oesophagus, NOS", "Carcinoma of upper third of esophagus", "malignant tumor of abdominal esophagus", "Carcinoma of upper third of oesophagus", "Malignant tumor of esophagus (disorder)", "Malignant Lower Third of Esophagus Tumor", "Malignant Middle Third of Esophagus Tumor", "esophageal squamous cell carcinoma, somatic", "Malignant Tumor of Upper Third of Esophagus", "Malignant tumor of upper third of esophagus", "Malignant Tumor of Lower Third of Esophagus", "malignant tumor of upper third of esophagus", "malignant neoplasm of upper third esophagus", "malignant neoplasm of esophagus (diagnosis)", "Malignant neoplasm of upper third esophagus", "Malignant Lower Third of Esophagus Neoplasm", "Malignant tumor of lower third of esophagus", "malignant tumor of lower third of esophagus", "Malignant tumor of middle third of esophagus", "Malignant Lower Third of the Esophagus Tumor", "Malignant neoplasm of esophagus, unspecified", "malignant tumor of middle third of esophagus", "malignant tumor of Distal Third of esophagus", "Malignant Tumor of Distal Third of Esophagus", "malignant tumor of distal third of esophagus", "Malignant Tumor of Middle Third of Esophagus", "Malignant neoplasm of upper third oesophagus", "Malignant Middle Third of Esophagus Neoplasm", "Aerodigestive tract cancer, susceptibility to", "Malignant Middle Third of the Esophagus Tumor", "Malignant tumour of lower third of oesophagus", "AERODIGESTIVE TRACT CANCER, SUSCEPTIBILITY TO", "Malignant tumour of upper third of oesophagus", "Malignant neoplasm of oesophagus, unspecified", "malignant tumor of proximal third of esophagus", "Malignant Neoplasm of Upper Third of Esophagus", "Malignant tumour of middle third of oesophagus", "Malignant neoplasm of lower third of esophagus", "malignant tumor of Proximal Third of esophagus", "Malignant neoplasm of upper third of esophagus", "Malignant Tumor of Proximal Third of Esophagus", "Malignant Neoplasm of Lower Third of Esophagus", "malignant neoplasm of lower third of esophagus", "malignant neoplasm of upper third of esophagus", "malignant neoplasm of lower third of oesophagus", "Malignant Lower Third of the Esophagus Neoplasm", "Malignant neoplasm of upper third of oesophagus", "malignant neoplasm of distal third of esophagus", "Malignant Neoplasm of Middle Third of Esophagus", "Malignant neoplasm of middle third of esophagus", "malignant neoplasm of middle third of esophagus", "Malignant neoplasm of distal third of esophagus", "Malignant Neoplasm of Distal Third of Esophagus", "Malignant neoplasm of lower third of oesophagus", "malignant neoplasm of middle third of oesophagus", "GASTRIC CARDIA ADENOCARCINOMA, SUSCEPTIBILITY TO", "Malignant Middle Third of the Esophagus Neoplasm", "gastric cardia adenocarcinoma, susceptibility to", "Malignant neoplasm of middle third of oesophagus", "Carcinoma of upper third of esophagus (disorder)", "Malignant neoplasm of esophagus, unspecified site", "malignant neoplasm of proximal third of esophagus", "Malignant neoplasm of proximal third of esophagus", "Malignant Neoplasm of Proximal Third of Esophagus", "Carcinoma of upper third of esophagus (diagnosis)", "Malignant Tumor of the Upper Third of the Esophagus", "esophageal neoplasm malignant carcinoma upper third", "Malignant Tumor of the Lower Third of the Esophagus", "Malignant Tumor of the Middle Third of the Esophagus", "malignant tumor of the middle third of the esophagus", "malignant tumor of the middle Third of the esophagus", "Malignant Tumor of the Distal Third of the Esophagus", "esophageal squamous cell carcinoma, susceptibility to", "ESOPHAGEAL SQUAMOUS CELL CARCINOMA, SUSCEPTIBILITY TO", "Malignant tumor of upper third of esophagus (disorder)", "Malignant tumor of lower third of esophagus (disorder)", "Malignant Neoplasm of the Lower Third of the Esophagus", "Malignant Tumor of the Proximal Third of the Esophagus", "Malignant Neoplasm of the Upper Third of the Esophagus", "Malignant Neoplasm of the Middle Third of the Esophagus", "Malignant Neoplasm of the Distal Third of the Esophagus", "Malignant tumor of middle third of esophagus (disorder)", "Malignant neoplasm of other specified part of esophagus", "Malignant Neoplasm of the Proximal Third of the Esophagus", "malignant neoplasm of lower third of esophagus (diagnosis)", "malignant neoplasm of upper third of esophagus (diagnosis)", "malignant neoplasm of middle third of esophagus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophageal cancer", "shortest_name_length": 16}
{"curie": "MONDO:0008228", "names": ["Addison anemia", "Biermer anemia", "Addison Anemia", "anemia; Biermer", "Addison; anemia", "Anemia, Addison", "Biermer disease", "Biermer; anemia", "anemia; Addison", "Addisons Anemia", "ANEMIA, BIERMER", "Addison anaemia", "Biermer's anemia", "Addison's Anemia", "Addison's anemia", "Anemia, Addisons", "addison's anemia", "malignant anemia", "malignant; anemia", "Anemia pernicious", "anemia pernicious", "Biermer's anaemia", "PERNICIOUS ANEMIA", "anemia; malignant", "addisonian anemia", "Anemia, Addison's", "Pernicious Anemia", "Pernicious anemia", "ANEMIA PERNICIOUS", "Addison's anaemia", "Addisonian anemia", "pernicious anemia", "pernicious anaemia", "Anaemia;pernicious", "pernicious; anemia", "ANAEMIA PERNICIOUS", "anemia; pernicious", "Addisonian anaemia", "Anaemia pernicious", "Anemia, Pernicious", "Pernicious anaemia", "ANEMIA, PERNICIOUS", "Pernicious anemia NOS", "PA - Pernicious anemia", "ANEMIA PERNICIOUS TYPE", "Anemia pernicious type", "Addison-Biermer anemia", "Pernicious anaemia NOS", "addison-biermer anemia", "Pernicious anemia, NOS", "Addison-Biermer anaemia", "Anaemia pernicious type", "PA - Pernicious anaemia", "Pernicious anaemia, NOS", "acquired pernicious anemia", "Intrinsic Factor Deficiency", "intrinsic factor deficiency", "Addisonian pernicious anemia", "Pernicious anemia (disorder)", "ANEMIA, ADDISONIAN PERNICIOUS", "Addisonian pernicious anaemia", "pernicious anemia (diagnosis)", "juvenile onset pernicious anemia", "Megaloblastic anemia due to impaired absorption of cobalamin", "Megaloblastic anaemia due to impaired absorption of cobalamin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pernicious anemia", "shortest_name_length": 14}
{"curie": "UMLS:C0410065", "names": [], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"]}
{"curie": "UMLS:C4316837", "names": ["Clear Cell Ameloblastoma", "Clear cell odontogenic tumor", "Clear Cell Odontogenic Tumor", "Clear Cell Odontogenic Carcinoma", "Clear cell odontogenic carcinoma", "Clear cell odontogenic carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clear cell odontogenic carcinoma", "shortest_name_length": 24}
{"curie": "UMLS:C5238975", "names": ["Phyllodes Tumor of Anogenital Mammary-Like Glands", "Phyllodes Tumor of Anogenital Mammary-Type Glands"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Phyllodes Tumor of Anogenital Mammary-Type Glands", "shortest_name_length": 49}
{"curie": "MONDO:0035357", "names": ["PSVD", "portosinusoidal vascular disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "portosinusoidal vascular disease", "shortest_name_length": 4}
{"curie": "UMLS:C3900057", "names": ["Allograft Thrombosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Allograft Thrombosis", "shortest_name_length": 20}
{"curie": "MONDO:0003633", "names": ["Malignant Mesenchymoma", "malignant mesenchymoma", "Malignant mesenchymoma", "Mesenchymoma, malignant", "MESENCHYMOMA, MALIGNANT", "mesenchymoma, malignant", "Mesenchymomas malignant", "malignant mesenchymomas", "Mixed mesenchymal sarcoma", "Malignant mesenchymoma NOS", "Malignant mesenchymal tumor", "malignant mesenchymoma (diagnosis)", "Malignant mesenchymoma stage unspecified", "mesenchymoma, malignant (morphologic abnormality)", "Mesenchymoma, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant mesenchymoma", "shortest_name_length": 22}
{"curie": "UMLS:C4721432", "names": ["Stage IV Nasopharyngeal Keratinizing Epidermoid Carcinoma", "Stage IV Keratinizing Epidermoid Carcinoma of Nasopharynx", "Stage IV Nasopharyngeal Keratinizing Squamous Cell Carcinoma", "Stage IV Keratinizing Squamous Cell Carcinoma of Nasopharynx", "Stage IV Keratinizing Epidermoid Carcinoma of the Nasopharynx", "Stage IV Keratinizing Squamous Cell Carcinoma of the Nasopharynx", "Stage IV Nasopharyngeal Throat Keratinizing Squamous Cell Cancer", "Stage IV Nasopharyngeal Keratinizing Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Nasopharyngeal Keratinizing Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 57}
{"curie": "UMLS:C0585955", "names": ["dysplasia larynx", "Dysplasia of Larynx", "Laryngeal dysplasia", "laryngeal dysplasia", "Dysplasia of larynx", "Dysplasia of larynx (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dysplasia of larynx", "shortest_name_length": 16}
{"curie": "MONDO:0060782", "names": ["premalignant hematologic condition", "Premalignant Hematologic Condition", "premalignant hematological system disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "premalignant hematological system disease", "shortest_name_length": 34}
{"curie": "MONDO:0010739", "names": ["TAQ1", "TaqI polymorphism", "Taqi polymorphism", "TaqI POLYMORPHISM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Taqi polymorphism", "shortest_name_length": 4}
{"curie": "UMLS:C1710414", "names": ["MMPTC", "Mixed medullary-papillary carcinoma", "mixed medullary-papillary thyroid carcinoma", "Mixed Medullary and Papillary Thyroid Carcinoma", "mixed medullary-papillary carcinoma of thyroid gland", "Thyroid Gland Mixed Medullary and Papillary Carcinoma", "mixed medullary-papillary thyroid carcinoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Mixed Medullary and Papillary Carcinoma", "shortest_name_length": 5}
{"curie": "MONDO:0001785", "names": ["malignant secondary hypertension", "secondary hypertension malignant", "Malignant secondary hypertension", "Secondary hypertension, malignant", "Accelerated secondary hypertension", "Malignant secondary hypertension NOS", "Malignant secondary hypertension (disorder)", "malignant secondary hypertension (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant secondary hypertension", "shortest_name_length": 32}
{"curie": "MONDO:0019625", "names": ["MEMA", "FTAAD", "Familial TAAD", "familial TAAD", "Erdheim disease", "cystic medionecrosis", "Cystic medionecrosis", "annuloaortic ectasia", "Medionecrosis of aorta", "Cystic Medial Necrosis", "cystic medial necrosis", "Cystic medial necrosis", "familial aortic aneurysm", "familial aortic dissection", "necrosis; aorta, cystic, medial", "Cystic medial necrosis of aorta", "aorta; necrosis, cystic, medial", "cystic medial necrosis of aorta", "Erdheim's cystic medial necrosis", "erdheim's cystic medial necrosis", "Familiar Thoracic Aortic Aneurysm", "familial thoracic aortic aneurysm", "Medionecrosis of aorta (disorder)", "Cystic medial necrosis of the aorta", "ERDHEIM CYSTIC MEDIAL NECROSIS OF AORTA", "Erdheim Cystic medial necrosis of aorta", "Erdheim cystic medial necrosis of aorta", "Mucoid extracellular matrix accumulation", "Medionecrosis aortae idiopathica cystica", "familial thoracic aortic aneurysm and dissection", "familial thoracic aortic aneurysm and aortic dissection", "Familial thoracic aortic aneurysm and aortic dissection", "Familial TAAD (thoracic aortic aneurysm aortic dissection)", "Familial thoracic aortic aneurysm and aortic dissection (disorder)", "Familial non-syndromic thoracic aortic aneurysm and aortic dissection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial thoracic aortic aneurysm and aortic dissection", "shortest_name_length": 4}
{"curie": "MONDO:0018648", "names": ["KOT", "KCOT", "KTOC", "Keratocyst", "keratocyst", "Keratocysts", "keratocysts", "Jaw Keratocyst", "Keratocyst of jaw", "Dental lamina cyst", "Odontogenic Keratocyst", "odontogenic keratocyst", "Keratocysts of the jaw", "odontogenic Keratocyst", "Odontogenic keratocyst", "keratocysts odontogenic", "Dental lamina keratocyst", "Odontogenic keratocystoma", "odontogenic keratocystoma", "OK - Odontogenic keratocyst", "Keratocystic odontogenic tumor", "Keratocystic Odontogenic Tumor", "keratocystic odontogenic tumor", "Odontogenic keratocysts of jaws", "Keratocystic odontogenic tumour", "Dental lamina cyst of the newborn", "Odontogenic keratocyst (disorder)", "Odontogenic keratocysts of the jaw", "odontogenic keratocyst (diagnosis)", "Odontogenic keratocyst (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Keratocystic odontogenic tumor", "shortest_name_length": 3}
{"curie": "MONDO:0008239", "names": ["PGM4", "Pgm4", "MILK PGM", "milk PGM", "PHOSPHOGLUCOMUTASE 4", "phosphoglucomutase 4", "phosphoglucomutase type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phosphoglucomutase 4", "shortest_name_length": 4}
{"curie": "MONDO:0000032", "names": ["FEB", "familial febrile seizures", "febrile seizures, familial", "seizures, familial febrile", "familial febrile convulsions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "febrile seizures, familial", "shortest_name_length": 3}
{"curie": "MONDO:0800032", "names": ["MTTL1 MELAS syndrome", "MELAS syndrome caused by mutation in MTTL1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MELAS syndrome caused by mutation in MTTL1", "shortest_name_length": 20}
{"curie": "MONDO:0008696", "names": ["Acanthosis nigricans muscle cramps acral enlargement", "acanthosis nigricans muscle cramps acral enlargement", "Acanthosis Nigricans With Muscle Cramps And Acral Enlargement", "ACANTHOSIS NIGRICANS WITH MUSCLE CRAMPS AND ACRAL ENLARGEMENT", "acanthosis nigricans with muscle cramps and acral enlargement", "acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome", "familial insulin resistance with acanthosis nigricans, acral hypertrophy and muscle cramps"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome", "shortest_name_length": 52}
{"curie": "MONDO:0006131", "names": ["CLNC", "lipomatous medulloblastoma", "Cerebellar liponeurocytoma", "Cerebellar Liponeurocytoma", "cerebellar liponeurocytoma", "Lipomatous Medulloblastoma", "Lipomatous medulloblastoma", "Liponeurocytoma of cerebellum", "lipomatous medulloblastoma (formerly)", "Cerebellar Liponeurocytoma (WHO Grade 2)", "Liponeurocytoma of cerebellum (disorder)", "cerebellar liponeurocytoma (WHO grade II)", "Cerebellar Liponeurocytoma (WHO Grade II)", "Cerebellar liponeurocytoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellar liponeurocytoma", "shortest_name_length": 4}
{"curie": "MONDO:0014870", "names": ["LCCS10", "NEK9-related lethal skeletal dysplasia", "lethal congenital contracture syndrome 10", "LETHAL CONGENITAL CONTRACTURE SYNDROME 10", "lethal congenital contracture syndrome type 10", "NIMA related kinase 9 lethal skeletal dysplasia", "NIMA related kinase 9 lethal skeletal dysplasia (disorder)", "Lethal skeletal dysplasia-fetal akinesia-contractures-thoracic dysplasia-pulmonary hypoplasia syndrome", "lethal skeletal dysplasia-fetal akinesia-contractures-thoracic dysplasia-pulmonary hypoplasia syndrome", "Lethal skeletal dysplasia, fetal akinesia, contractures, thoracic dysplasia, pulmonary hypoplasia syndrome", "Lethal skeletal dysplasia, foetal akinesia, contractures, thoracic dysplasia, pulmonary hypoplasia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "NEK9-related lethal skeletal dysplasia", "shortest_name_length": 6}
{"curie": "MONDO:0020773", "names": ["CSF rhinorrhea", "CSF Rhinorrhea", "Rhinorrhea, CSF", "CSF Rhinorrheas", "CSF rhinorrhoea", "Rhinorrheas, CSF", "Cerebrospinal Rhinorrhea", "Cerebrospinal rhinorrhea", "cerebrospinal rhinorrhea", "rhinorrhea; cerebrospinal", "cerebrospinal; rhinorrhea", "Cerebrospinal rhinorrhoea", "Rhinorrhea, Cerebrospinal", "Cerebrospinal Rhinorrheas", "Rhinorrheas, Cerebrospinal", "CSF - Cerebrospinal rhinorrhea", "cerebrospinal fluid rhinorrhea", "Cerebrospinal fluid rhinorrhea", "Cerebrospinal Fluid Rhinorrhea", "csf - cerebrospinal rhinorrhea", "CSF - Cerebrospinal rhinorrhoea", "Rhinorrhea, Cerebrospinal Fluid", "Cerebrospinal fluid rhinorrhoea", "Cerebrospinal Fluid Rhinorrheas", "cerebrospinal fluid rhinorrhoea", "Rhinorrheas, Cerebrospinal Fluid", "Traumatic Cerebrospinal Fluid Rhinorrhea", "Rhinorrhea, Traumatic Cerebrospinal Fluid", "Cerebrospinal fluid rhinorrhea (disorder)", "Traumatic Rhinorrhea, Cerebrospinal Fluid", "Cerebrospinal Fluid Rhinorrhea, Traumatic", "Spontaneous Cerebrospinal Fluid Rhinorrhea", "cerebrospinal fluid rhinorrhea (diagnosis)", "Rhinorrhea, Cerebrospinal Fluid, Traumatic", "Spontaneous Rhinorrhea, Cerebrospinal Fluid", "Cerebrospinal Fluid Rhinorrhea, Spontaneous", "Rhinorrhea, Spontaneous Cerebrospinal Fluid", "Rhinorrhea, Cerebrospinal Fluid, Spontaneous", "post Traumatic Cerebrospinal Fluid Rhinorrhea", "post-Traumatic Cerebrospinal Fluid Rhinorrhea", "Cerebrospinal Fluid Rhinorrhea, post Traumatic", "post-Traumatic Rhinorrhea, Cerebrospinal Fluid", "Cerebrospinal Fluid Rhinorrhea, post-Traumatic", "post Traumatic Rhinorrhea, Cerebrospinal Fluid", "Rhinorrhea, post-Traumatic, Cerebrospinal Fluid", "Rhinorrhea, Cerebrospinal Fluid, post-Traumatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebrospinal fluid rhinorrhea", "shortest_name_length": 14}
{"curie": "MONDO:0700188", "names": ["Feline Synovial Cell Sarcoma", "feline synovial cell sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "feline synovial cell sarcoma", "shortest_name_length": 28}
{"curie": "UMLS:C4526917", "names": ["LUSC-CIS", "Squamous Cell Lung Carcinoma In Situ", "Lung Squamous Cell Carcinoma In Situ"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Squamous Cell Carcinoma In Situ", "shortest_name_length": 8}
{"curie": "MONDO:0010534", "names": ["Scax4", "SCAX4", "X-linked ataxia-dementia syndrome", "ataxia-dementia syndrome X-linked", "X-linked ataxia dementia syndrome", "X-linked spinocerebellar ataxia 4", "SPINOCEREBELLAR ATAXIA, X-LINKED 4", "Ataxia-dementia syndrome, X-linked", "ATAXIA-DEMENTIA SYNDROME, X-LINKED", "spinocerebellar ataxia, X-linked 4", "Spinocerebellar Ataxia, X-Linked 4", "ataxia-dementia syndrome, X-linked", "Spinocerebellar ataxia, X-linked, 4", "X-linked spinocerebellar ataxia type 4", "spinocerebellar ataxia X-linked type 4", "spinocerebellar ataxia, X-linked type 4", "X-linked spinocerebellar ataxia type 4 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked spinocerebellar ataxia type 4", "shortest_name_length": 5}
{"curie": "UMLS:C0424813", "names": ["edema; orbit", "orbit; edema", "Swollen orbit", "orbital edema", "swollen orbit", "Orbital edema", "Edema of orbit", "Orbital oedema", "orbital oedema", "orbital swelling", "Orbital swelling", "Orbital edema (disorder)", "orbital edema (diagnosis)", "Edema of unspecified orbit", "Orbital edema or congestion", "Orbital swelling (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Orbital edema", "shortest_name_length": 12}
{"curie": "MONDO:0014272", "names": ["PPKN", "PPK, Nagashima type", "Palmoplantar keratoderma Nagashima type", "Palmoplantar keratoderma, Nagashima type", "PALMOPLANTAR KERATODERMA, NAGASHIMA TYPE", "palmoplantar keratoderma, Nagashima type", "palmoplantar hyperkeratosis, Nagashima type", "Palmoplantar hyperkeratosis, Nagashima type", "Palmoplantar keratoderma Nagashima type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "palmoplantar keratoderma, Nagashima type", "shortest_name_length": 4}
{"curie": "MONDO:0013830", "names": ["KTCN5", "keratoconus 5", "KERATOCONUS 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratoconus 5", "shortest_name_length": 5}
{"curie": "UMLS:C1707402", "names": ["Classical Low Grade Fibromyxoid Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Classical Low Grade Fibromyxoid Sarcoma", "shortest_name_length": 39}
{"curie": "MONDO:0008464", "names": ["ECD", "SHSF1", "SHFM1", "SHFD1", "ECTRODACTYLY", "ectrodactyly", "split-hand deformity", "SPLIT-HAND DEFORMITY", "split-hand/foot deformity 1", "SPLIT-HAND/FOOT DEFORMITY 1", "Split-Hand-Foot Deformity 1", "Split hand foot deformity 1", "Split-Hand-Foot Malformation 1", "SPLIT-HAND/FOOT MALFORMATION 1", "split-hand/foot malformation 1", "Split hand foot malformation 1", "split hand-foot malformation 1", "Split-Hand/Foot Malformation 1", "split hand/foot malformation 1", "Split-Hand/Foot Malformation Type 1", "split hand-foot malformation type 1", "split-hand/foot malformation type 1", "split-hand/foot malformation 1 with or without deafness", "SPLIT-HAND/FOOT MALFORMATION 1 WITH OR WITHOUT DEAFNESS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "split hand-foot malformation 1", "shortest_name_length": 3}
{"curie": "UMLS:C0431943", "names": ["leg; deformity, congenital", "deformity; leg, congenital", "Congenital deformity of leg", "congenital deformity of lower limb", "Congenital deformity of lower limb", "Lower Limb Deformities, Congenital", "Lower Extremity Deformities, Congenital", "Congenital deformity of lower limb (disorder)", "congenital deformity of lower limb (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lower Extremity Deformities, Congenital", "shortest_name_length": 26}
{"curie": "UMLS:C1561982", "names": ["TASS", "Toxic anterior segment syndrome", "Toxic Anterior Segment Syndrome", "Toxic Anterior Segment Syndrome (TASS)", "TASS - toxic anterior segment syndrome", "Toxic anterior segment syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Toxic anterior segment syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0100474", "names": ["mild ichthyosis vulgaris"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mild ichthyosis vulgaris", "shortest_name_length": 24}
{"curie": "MONDO:0005593", "names": ["chronic periodontitis", "Chronic Periodontitis", "periodontitis, chronic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic periodontitis", "shortest_name_length": 21}
{"curie": "MONDO:0060732", "names": ["TETAMS2", "TETRAAMELIA SYNDROME 2", "tetraamelia syndrome 2", "tetraamelia with pulmonary hypoplasia", "tetra-amelia with pulmonary hypoplasia", "TETRAAMELIA SYNDROME 2 WITH PULMONARY AGENESIS", "tetraamelia syndrome 2 with pulmonary agenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tetraamelia syndrome 2", "shortest_name_length": 7}
{"curie": "MONDO:0008346", "names": ["sideroses", "Sideroses", "siderosis", "Siderosis", "brown lung", "Welders' lung", "Iron oxide lung", "brown induration", "Arc-welders' lung", "arc-welder's lung", "Welders' siderosis", "iron pneumoconiosis", "Iron pneumoconiosis", "Pulmonary siderosis", "pulmonary siderosis", "arc-welders' disease", "Arc-welders' disease", "Siderotic lung disease", "PULMONARY HEMOSIDEROSIS", "pulmonary hemosiderosis", "Steel grinders' disease", "hemosiderosis pulmonary", "Pulmonary hemosiderosis", "Arc-welders' nodulation", "Brown induration of lung", "pulmonary haemosiderosis", "Pulmonary haemosiderosis", "Pneumoconiosis siderotico", "Arc welder's lung disease", "Arc-welders' pneumoconiosis", "Pulmonary siderosis (disorder)", "lung; fibrosis, with siderosis", "fibrosis; lung, with siderosis", "pulmonary siderosis (diagnosis)", "LUNG, ESSENTIAL BROWN INDURATION", "siderosis (arc welders' disease)", "alveolar hypoventilation syndrome", "Idiopathic pulmonary hemosiderosis", "alveolar; hypoventilation syndrome", "idiopathic pulmonary hemosiderosis", "syndrome; alveolar hypoventilation", "Essential brown induration of lung", "PULMONARY HEMOSIDEROSIS IDIOPATHIC", "Idiopathic pulmonary haemosiderosis", "HEMOSIDEROSIS, PULMONARY, IDIOPATHIC", "IPH - Idiopathic pulmonary hemosiderosis", "IPH - Idiopathic pulmonary haemosiderosis", "Idiopathic pulmonary hemosiderosis (disorder)", "idiopathic pulmonary hemosiderosis (diagnosis)", "hemosiderosis, pulmonary, with deficiency of gamma-a globulin", "HEMOSIDEROSIS, PULMONARY, WITH DEFICIENCY OF GAMMA-A GLOBULIN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary hemosiderosis", "shortest_name_length": 9}
{"curie": "UMLS:C5441547", "names": ["DCIS and ILC", "DCIS and Infiltrating Lobular Carcinoma", "Non-Infiltrating Ductal Carcinoma and ILC", "Infiltrating lobular mixed with other types of carcinoma", "Ductal Carcinoma in situ and Infiltrating Lobular Carcinoma", "Ductal Breast Carcinoma In Situ and Invasive Lobular Carcinoma", "Breast Ductal Carcinoma In Situ and Invasive Lobular Carcinoma", "Non-Infiltrating Ductal Carcinoma and Infiltrating Lobular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Ductal Carcinoma In Situ and Invasive Lobular Carcinoma", "shortest_name_length": 12}
{"curie": "UMLS:C4553884", "names": ["Stage IVB Thyroid Gland Medullary Cancer", "Stage IVB Thyroid Gland Medullary Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Thyroid Gland Medullary Carcinoma AJCC v8", "shortest_name_length": 40}
{"curie": "UMLS:C5446923", "names": ["Invasive Breast Solid Papillary Carcinoma", "Breast Solid Papillary Carcinoma with Invasion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Invasive Breast Solid Papillary Carcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0100089", "names": ["GATA1-Related Cytopenia", "GATA1-Related X-Linked Cytopenia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "GATA1-Related X-Linked Cytopenia", "shortest_name_length": 23}
{"curie": "MONDO:0003887", "names": ["ovary mucinous adenofibroma", "Ovarian Mucinous Adenofibroma", "ovarian mucinous adenofibroma", "mucinous adenofibroma of ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian mucinous adenofibroma", "shortest_name_length": 27}
{"curie": "UMLS:C1304507", "names": ["Sinusoidal hemangioma", "Sinusoidal Hemangioma", "Sinusoidal haemangioma", "Sinusoidal hemangioma (disorder)", "Sinusoidal hemangioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinusoidal hemangioma", "shortest_name_length": 21}
{"curie": "UMLS:C0025570", "names": ["Epidermalisation", "Epidermalization", "Squamous Metaplasia", "metaplasia squamous", "SQUAMOUS METAPLASIA", "squamous metaplasia", "Squamous metaplasia", "Sinonasal metaplasia", "Metaplasia, squamous", "Epidermoid metaplasia", "Squamous metaplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Squamous metaplasia", "shortest_name_length": 16}
{"curie": "UMLS:C0264879", "names": ["Valvular insufficiency", "Valvular Regurgitation", "valvular insufficiency", "Valvular Insufficiency", "Heart valve incompetence", "heart valve incompetence", "heart valve insufficiency", "Heart valve regurgitation", "Heart valve insufficiency", "Heart Valve Regurgitation", "heart valve regurgitation", "heart regurgitation valve", "heart valve; insufficiency", "heart regurgitation valves", "Cardiac valve insufficiency", "heart; insufficiency, valve", "cardiac valve insufficiency", "Valvular regurgitation, NOS", "Heart valve incompetence, NOS", "Heart valve regurgitation, NOS", "Heart valve insufficiency, NOS", "Heart valve regurgitation (disorder)", "Valvular Insufficiency/ Regurgitation", "heart valve regurgitation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Heart valve regurgitation", "shortest_name_length": 22}
{"curie": "MONDO:0017416", "names": ["polio late effects", "Postpolio syndrome", "Postpolio sequelae", "POSTPOLIO SYNDROME", "postpolio syndrome", "postpolio sequelae", "post polio syndrome", "post-polio syndrome", "Post-polio Syndrome", "Post-Polio Syndrome", "Post polio syndrome", "polio post syndrome", "post-polio sequelae", "Post-Polio Syndromes", "postpoliomyelitic syndrome", "Postpolio muscular atrophy", "Postpoliomyelitis syndrome", "postpoliomyelitis syndrome", "postpoliomyelitis sequelae", "Postpoliomyelitic syndrome", "Postpoliomyelitis sequelae", "Postpoliomyelitis Syndrome", "post poliomyelitis syndrome", "post-poliomyelitic syndrome", "postpolio myelitic syndrome", "Post Poliomyelitis Syndrome", "post-polio muscular atrophy", "Post-Poliomyelitis Syndrome", "Post poliomyelitis syndrome", "post-polio syndrome (diagnosis)", "Postpoliomyelitis Muscular Atrophy", "Post Poliomyelitis Muscular Atrophy", "Muscular Atrophy, Postpoliomyelitis", "Post-Poliomyelitis Muscular Atrophy", "Muscular Atrophy, Post-Poliomyelitis", "Postpoliomyelitis Muscular Atrophies", "Post-Poliomyelitis Muscular Atrophies", "Muscular Atrophies, Postpoliomyelitis", "Post poliomyelitis syndrome (disorder)", "Muscular Atrophies, Post-Poliomyelitis", "Post-polio progressive muscular atrophy", "Progressive muscular atrophy following poliomyelitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postpoliomyelitis syndrome", "shortest_name_length": 18}
{"curie": "MONDO:0013337", "names": ["HSN1C", "HSN 1C", "HSN IC", "HSAN1C", "HSAN IC", "HSAN 1C", "NEUROPATHY, HEREDITARY SENSORY, TYPE IC", "neuropathy, hereditary sensory, type 1C", "Hereditary sensory autonomic neuropathy type IC", "hereditary sensory and autonomic neuropathy type IC", "hereditary sensory and autonomic neuropathy type 1C", "neuropathy, hereditary sensory and autonomic, type 1C", "neuropathy, hereditary sensory and autonomic, type IC", "NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC", "Hereditary sensory autonomic neuropathy type IC (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuropathy, hereditary sensory and autonomic, type 1C", "shortest_name_length": 5}
{"curie": "MONDO:0020808", "names": ["androblastoma of testis", "testicular androblastoma", "Sertoli cell tumor of testis", "Sertoli Cell Tumor of Testis", "testicular sertoli cell tumor", "Sertoli cell tumour of testis", "Testicular Sertoli Cell Tumor", "Sertoli cell testicular tumor", "Sertoli cell testicular tumour", "Sertoli cell testicular tumors", "Sertoli Cell Neoplasm of Testis", "Sertoli cell neoplasm of testis", "Testicular Sertoli Cell Neoplasm", "Sertoli Cell Tumor of the Testis", "Testicular Sertoli Cell Tumor, NOS", "androblastoma of testis (diagnosis)", "Sertoli Cell Neoplasm of the Testis", "Sertoli cell tumor of testis (disorder)", "Testicular Sertoli Cell Tumor, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular sertoli cell tumor", "shortest_name_length": 23}
{"curie": "MONDO:0000638", "names": ["benign glioma", "glioma, benign"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign glioma", "shortest_name_length": 13}
{"curie": "UMLS:C1112747", "names": ["HbSE disease", "HbS-HbE disease", "Hemoglobin SE disease", "Hemoglobin SE Disease", "Hemoglobin S/E disease", "Hemoglobin S-E disease", "Haemoglobin SE disease", "Haemoglobin S-E disease", "Haemoglobin S/E disease", "sickle cell-hemoglobin E disease", "Sickle Cell-Hemoglobin E Disease", "Sickle cell-hemoglobin E disease", "Sickle cell-haemoglobin E disease", "Double heterozygous for Hb S + Hb E", "anemia hemolytic sickle Hb-E disease", "Sickle cell-hemoglobin E disease syndrome", "Sickle cell-hemoglobin E disease (disorder)", "Sickle cell anemia with hemoglobin E disease", "sickle cell-hemoglobin E disease (diagnosis)", "Sickle cell anaemia with haemoglobin E disease", "disease (or disorder); hemoglobin or Hb, E (Hb-E) sickle-cell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemoglobin SE disease", "shortest_name_length": 12}
{"curie": "UMLS:C4726605", "names": ["Mixed Phenotype Acute Leukemia, NOS, Rare Subtypes", "Mixed Phenotype Acute Leukemia, Not Otherwise Specified, Rare Subtypes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mixed Phenotype Acute Leukemia, Not Otherwise Specified, Rare Subtypes", "shortest_name_length": 50}
{"curie": "MONDO:0003376", "names": ["mediastinal leiomyosarcoma", "Mediastinal Leiomyosarcoma", "mediastinum leiomyosarcoma", "Leiomyosarcoma of Mediastinum", "leiomyosarcoma of mediastinum", "Leiomyosarcoma of the Mediastinum", "leiomyosarcoma of the mediastinum", "leiomyosarcoma of mediastinum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mediastinum leiomyosarcoma", "shortest_name_length": 26}
{"curie": "MONDO:0007047", "names": ["ake", "TIA", "AKE", "NTIA", "PPKP3", "acrokeratoelastoidosis", "ACROKERATOELASTOIDOSIS", "Acrokerato-elastoidosis", "aganglionosis, total colonic", "Acrokeratoelastoidosis of Costa", "acrokeratoelastoidosis of Costa", "Acrokerato-elastoidosis (disorder)", "near-total intestinal aganglionosis", "rare form of Hirschsprung's disease", "Collagenous plaques of hand and feet", "collagenous plaques of hand and feet", "COLLAGENOUS PLAQUES OF HANDS AND FEET", "Collagenous Plaques Of Hands And Feet", "collagenous plaques of hands and feet", "Punctate palmoplantar keratoderma type 3", "punctate palmoplantar keratoderma type 3", "Collagenous plaques of the hands and feet", "Palmoplantar keratoderma, punctate type 3", "palmoplantar keratoderma, punctate type 3", "keratoderma, palmoplantar, punctate type 3", "punctate palmoplantar keratoderma type III", "punctate palmoplantar hyperkeratosis type 3", "PALMOPLANTAR KERATODERMA, PUNCTATE TYPE III", "Punctate palmoplantar hyperkeratosis type 3", "acrokeratoelastoidosis of Costa (diagnosis)", "palmoplantar keratoderma, punctate type III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "punctate palmoplantar keratoderma type III", "shortest_name_length": 3}
{"curie": "MONDO:0011316", "names": ["osteosclerotic chondrodysplasia, lethal, with intracellular inclusions", "OSTEOSCLEROTIC CHONDRODYSPLASIA, LETHAL, WITH INTRACELLULAR INCLUSIONS", "Osteosclerotic Chondrodysplasia, Lethal, With Intracellular Inclusions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteosclerotic chondrodysplasia, lethal, with intracellular inclusions", "shortest_name_length": 70}
{"curie": "UMLS:C3645711", "names": ["Congenital Osteopetrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Osteopetrosis", "shortest_name_length": 24}
{"curie": "UMLS:C3274498", "names": ["Lithium Induced Birth Defect", "Lithium-Induced Birth Defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lithium Induced Birth Defect", "shortest_name_length": 28}
{"curie": "MONDO:0023018", "names": ["dupont sellier chochillon syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dupont sellier chochillon syndrome", "shortest_name_length": 34}
{"curie": "MONDO:0020412", "names": ["Congenital patent ductus arteriosus aneurysm", "congenital patent ductus arteriosus aneurysm", "Congenital patent ductus arteriosus aneurysm (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital patent ductus arteriosus aneurysm", "shortest_name_length": 44}
{"curie": "MONDO:0700164", "names": ["Canine Nephroblastoma", "canine nephroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canine nephroblastoma", "shortest_name_length": 21}
{"curie": "UMLS:C1333872", "names": ["Granular Cell Odontogenic Fibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Granular Cell Odontogenic Fibroma", "shortest_name_length": 33}
{"curie": "MONDO:0002564", "names": ["jejunum tumor", "Jejunal Tumor", "jejunal tumor", "Jejunal tumor", "jejunum neoplasm", "Jejunal Neoplasm", "Tumor of jejunum", "jejunal neoplasm", "Tumor of Jejunum", "tumor of jejunum", "Jejunal Neoplasms", "Neoplasm, Jejunal", "Tumour of jejunum", "Neoplasms, Jejunal", "Neoplasm of jejunum", "Neoplasm of Jejunum", "neoplasm of jejunum", "Tumor of the Jejunum", "tumor of the jejunum", "neoplasm of the jejunum", "Neoplasm of the Jejunum", "jejunum neoplasm (disease)", "Neoplasm of jejunum (disorder)", "neoplasm of jejunum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "jejunal neoplasm", "shortest_name_length": 13}
{"curie": "MONDO:0012507", "names": ["RCD4", "CACNA2D4 cone dystrophy", "retinal cone dystrophy 4", "Retinal Cone Dystrophy 4", "RETINAL CONE DYSTROPHY 4", "retinal cone dystrophy type 4", "cone dystrophy caused by mutation in CACNA2D4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal cone dystrophy 4", "shortest_name_length": 4}
{"curie": "MONDO:0018373", "names": ["AVN", "Aseptic necrosis", "ischemic necrosis", "Avascular necrosis", "ischaemic necrosis", "avascular necrosis", "Ischemic bone necrosis", "avascular bone necrosis", "BONE NECROSIS AVASCULAR", "avascular necrosis bone", "Bone Avascular Necrosis", "Ischaemic bone necrosis", "avascular; bone necrosis", "avascular; osteonecrosis", "avascular bones necrosis", "osteonecrosis; avascular", "necrosis; bone, avascular", "avascular necrosis of bone", "Avascular necrosis of bone", "Avascular Necrosis of Bone", "Necrosis, Avascular, of Bone", "avascular necrosis (diagnosis)", "AVN - Avascular necrosis of bone", "Avascular necrosis of bone (disorder)", "Death of bone due to decreased blood supply"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "avascular necrosis", "shortest_name_length": 3}
{"curie": "MONDO:0009874", "names": ["Mendenhall Syndrome", "Mendenhall syndrome", "MENDENHALL SYNDROME", "Syndrome, Mendenhall", "Rabson-Mendenhall Syndrome", "Rabson-Mendenhall syndrome", "Rabson Mendenhall Syndrome", "Rabson Mendenhall syndrome", "RABSON-MENDENHALL SYNDROME", "Syndrome, Rabson-Mendenhall", "Pineal hyperplasia AND diabetes mellitus syndrome", "Pineal hyperplasia and diabetes mellitus syndrome", "Pineal hyperplasia AND diabetes mellitus syndrome (disorder)", "Pineal hyperplasia AND diabetes mellitus syndrome (diagnosis)", "diabetes mellitus associated with genetic syndrome pineal hyperplasia", "Pineal hyperplasia, insulin-resistant diabetes mellitus and somatic abnormalities", "PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES", "Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, And Somatic Abnormalities", "pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rabson-Mendenhall syndrome", "shortest_name_length": 19}
{"curie": "UMLS:C1519508", "names": ["Stage II Centroblastic Follicular Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Centroblastic Follicular Lymphoma", "shortest_name_length": 42}
{"curie": "UMLS:C4330509", "names": ["K ATP Channel-Associated Diabetes Mellitus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "K ATP Channel-Associated Diabetes Mellitus", "shortest_name_length": 42}
{"curie": "UMLS:C2982480", "names": ["Stage III Hypopharyngeal Carcinoma", "Stage III Hypopharyngeal Throat Cancer", "Stage III Hypopharyngeal Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Hypopharyngeal Carcinoma AJCC v7", "shortest_name_length": 34}
{"curie": "MONDO:0018555", "names": ["nIHH", "hypogonadotropism", "central hypogonadism", "Central Hypogonadism", "secondary hypogonadism", "Secondary hypogonadism", "Secondary Hypogonadism", "gonadotropic deficiency", "Gonadotrophin deficiency", "Secondary hypogonadism, NOS", "secondary testicular failure", "Hypogonadotropic Hypogonadism", "Hypogonadotropic hypogonadism", "hypogonadotropic hypogonadism", "hypogonadotrophic hypogonadism", "Hypogonadism, hypogonadotropic", "Hypogonadism, Hypogonadotropic", "hypogonadotropic; hypogonadism", "Hypogonadotrophic hypogonadism", "hypogonadism, hypogonadotropic", "isolated hypogonadotropic hypogonadism", "Isolated hypogonadotropic hypogonadism", "Gonadotropin deficiency syndrome, male", "Isolated Hypogonadotropic Hypogonadism", "Hypogonadism, Isolated Hypogonadotropic", "HYPOGONADISM, ISOLATED HYPOGONADOTROPIC", "Hypogonadotropic hypogonadism (disorder)", "secondary testicular failure (diagnosis)", "hypogonadotropic hypogonadism (diagnosis)", "low gonadotropins (secondary hypogonadism)", "Low gonadotropins (secondary hypogonadism)", "isolated congenital gonadotropin deficiency", "normosmic congenital hypogonadotropic hypogonadism", "Normosmic idiopathic hypogonadotropic hypogonadism", "congenital idiopathic hypogonadotropic hypogonadism", "hypogonadotropic hypogonadism with or without anosmia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadotropic hypogonadism", "shortest_name_length": 4}
{"curie": "MONDO:0100044", "names": ["AFFND1", "AFFN dysostosis 1", "AFFN DYSOSTOSIS 1", "Acrofrontofacionasal Dysostosis 1", "acrofrontofacionasal dysostosis 1", "ACROFRONTOFACIONASAL DYSOSTOSIS 1", "acrofrontofacionasal dysostosis type 1", "Acrofrontofacionasal dysostosis syndrome", "Polysyndactyly, postaxial, frontonasal dysostosis, and cleft lip-palate", "POLYSYNDACTYLY, POSTAXIAL, FRONTONASAL DYSOSTOSIS, AND CLEFT LIP/PALATE", "Cleft lip-palate with frontonasal dysostosis and postaxial polysyndactyly", "CLEFT LIP/PALATE WITH FRONTONASAL DYSOSTOSIS AND POSTAXIAL POLYSYNDACTYLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acrofrontofacionasal dysostosis 1", "shortest_name_length": 6}
{"curie": "MONDO:0003294", "names": ["pericardial leiomyoma", "pericardium leiomyoma", "Pericardial Leiomyoma", "leiomyoma of pericardium", "leiomyoma of Pericardium", "Leiomyoma of Pericardium", "leiomyoma of the pericardium", "Leiomyoma of the Pericardium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pericardium leiomyoma", "shortest_name_length": 21}
{"curie": "MONDO:0021323", "names": ["chest wall cancer", "cancer of chest wall", "Malignant Chest Wall Tumor", "malignant chest wall tumor", "malignant tumor of chest wall", "Malignant Chest Wall Neoplasm", "Malignant Tumor of Chest Wall", "malignant chest wall neoplasm", "Malignant Neoplasm of Chest Wall", "Malignant neoplasm of chest wall", "malignant neoplasm of chest wall", "Malignant Tumor of the Chest Wall", "malignant tumor of the chest wall", "malignant neoplasm of the chest wall", "Malignant Neoplasm of the Chest Wall", "Malignant neoplasm of chest wall NOS", "Malignant neoplasm of chest wall, NOS", "Malignant neoplasm of chest wall (disorder)", "malignant neoplasm of chest wall (diagnosis)", "malignant neoplasm of ill-defined site chest wall"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant neoplasm of chest wall", "shortest_name_length": 17}
{"curie": "MONDO:0014533", "names": ["DEE28", "EIEE28", "WOREE syndrome", "WWOX-related epileptic encephalopathy", "early infantile epileptic encephalopathy 28", "Early Infantile Epileptic Encephalopathy 28", "epileptic encephalopathy, early infantile, 28", "Developmental and Epileptic Encephalopathy 28", "developmental and epileptic encephalopathy 28", "WWOX early infantile epileptic encephalopathy", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 28", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28", "developmental and epileptic encephalopathy, 28", "epileptic encephalopathy, early infantile, type 28", "early infantile epileptic encephalopathy caused by mutation in WWOX"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 28", "shortest_name_length": 5}
{"curie": "MONDO:0014952", "names": ["NEDHELS", "DYSEIDD", "intellectual disability-epilepsy-extrapyramidal syndrome", "DYSKINESIA, SEIZURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER", "dyskinesia, seizures, and intellectual developmental disorder", "neurodevelopmental disorder with hypotonia, impaired expressive language, and with or without seizures", "NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND IMPAIRED EXPRESSIVE LANGUAGE AND WITH OR WITHOUT SEIZURES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability-epilepsy-extrapyramidal syndrome", "shortest_name_length": 7}
{"curie": "MONDO:0015504", "names": ["larynx anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "larynx anomaly", "shortest_name_length": 14}
{"curie": "UMLS:C0278568", "names": ["Skin T-Cell Lymphoma Stage II", "T-Cell Lymphoma of Skin Stage II", "stage II cutaneous T-cell lymphoma", "Cutaneous T-cell lymphoma stage II", "Cutaneous T-Cell Lymphoma Stage II", "cutaneous T-cell lymphoma, stage II", "T-Cell Lymphoma of the Skin Stage II", "stage II cutaneous T-cell non-Hodgkin lymphoma", "Stage II Cutaneous T-Cell Non-Hodgkin Lymphoma", "Stage II Cutaneous T-Cell Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous T-cell lymphoma stage II", "shortest_name_length": 29}
{"curie": "MONDO:0013911", "names": ["HH9", "NSMF hypogonadotropic hypogonadism", "hypogonadotropic hypogonadism 9 with or without anosmia", "HYPOGONADOTROPIC HYPOGONADISM 9 WITH OR WITHOUT ANOSMIA", "hypogonadotropic hypogonadism caused by mutation in NSMF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadotropic hypogonadism 9 with or without anosmia", "shortest_name_length": 3}
{"curie": "MONDO:0012583", "names": ["STHAG5", "HE-ZHAO DEFICIENCY", "he-Zhao deficiency", "He-Zhao Deficiency", "Hypodontia-Oligodontia 5", "hypodontia/oligodontia 5", "HYPODONTIA/OLIGODONTIA 5", "TOOTH AGENESIS, SELECTIVE, 5", "Tooth Agenesis, Selective, 5", "tooth agenesis, selective, 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tooth agenesis, selective, 5", "shortest_name_length": 6}
{"curie": "UMLS:C2931277", "names": ["Pena Shokeir syndrome Type 2", "Pena-Shokeir syndrome type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pena Shokeir syndrome Type 2", "shortest_name_length": 28}
{"curie": "MONDO:0007088", "names": ["AD", "AD1", "Alzheimer disease", "Alzheimer disease 1", "Alzheimer's Disease 1", "Alzheimer's disease 1", "Alzheimer disease type 1", "presenile and senile dementia", "PRESENILE AND SENILE DEMENTIA", "Alzheimer disease 1, familial", "Alzheimer disease, familial, 1", "ALZHEIMER DISEASE, FAMILIAL, 1", "Alzheimer Disease, Familial, 1", "Alzheimer's disease 1, early onset", "Alzheimer disease, susceptibility to", "Familial Alzheimer's Disease, Type 1", "Alzheimer disease, protection against", "ALZHEIMER DISEASE, PROTECTION AGAINST", "early-onset familial form of Alzheimer disease", "Early-onset familial form of Alzheimer disease", "Alzheimer disease, late-onset, susceptibility to", "Alzheimer disease, early-onset, with cerebral amyloid angiopathy", "ALZHEIMER DISEASE, EARLY-ONSET, WITH CEREBRAL AMYLOID ANGIOPATHY", "Alzheimer Disease, Early-Onset, With Cerebral Amyloid Angiopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alzheimer disease type 1", "shortest_name_length": 2}
{"curie": "UMLS:C4727415", "names": ["Recurrent Submandibular Gland Adenoid Cystic Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Submandibular Gland Adenoid Cystic Carcinoma", "shortest_name_length": 54}
{"curie": "MONDO:0016823", "names": ["MYCETOMA", "mycetoma", "Mycetoma", "mycetomas", "Mycetomata", "Madura foot", "madura foot", "Mycetoma NOS", "maduramycosis", "Mycetoma, NOS", "maduromycosis", "fungal mycetoma", "Mycetoma (disorder)", "mycetoma (diagnosis)", "Mycetoma, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mycetoma", "shortest_name_length": 8}
{"curie": "UMLS:C1332625", "names": ["Metastatic Breast Cancer in the Liver", "Breast Carcinoma Metastatic in the Liver", "Breast Carcinoma Metastatic to the Liver"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Carcinoma Metastatic in the Liver", "shortest_name_length": 37}
{"curie": "UMLS:C1336006", "names": ["Small Intestinal Non-Hodgkin Lymphoma", "Small Intestine Non-Hodgkin's Lymphoma", "Small Intestinal Non-Hodgkin's Lymphoma", "non-Hodgkin's lymphoma of small intestine", "Primary Small Intestinal Non-Hodgkin's Lymphoma", "non-Hodgkin's lymphoma of small intestine (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-Hodgkin's lymphoma of small intestine", "shortest_name_length": 37}
{"curie": "UMLS:C0752200", "names": ["Autosomal Dominant Familial Dystonia", "Familial Dystonia, Autosomal Dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Autosomal Dominant Familial Dystonia", "shortest_name_length": 36}
{"curie": "MONDO:0009418", "names": ["Hypogonadism with Low-Grade Mental Deficiency and Microcephaly", "HYPOGONADISM WITH LOW-GRADE MENTAL DEFICIENCY AND MICROCEPHALY", "hypogonadism with low-grade mental deficiency and microcephaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadism with low-grade mental deficiency and microcephaly", "shortest_name_length": 62}
{"curie": "MONDO:0035441", "names": ["CARST", "congenital autosomal recessive small-platelet thrombocytopenia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital autosomal recessive small-platelet thrombocytopenia", "shortest_name_length": 5}
{"curie": "UMLS:C1336139", "names": ["stage IB non-small cell lung cancer", "Stage IB Non-Small Cell Lung Cancer", "Stage IB Non-Oat Cell Lung Carcinoma", "Stage IB Non-Small Cell Lung Carcinoma", "Stage IB Non-Oat Cell Carcinoma of Lung", "Stage IB Non-Small Cell Carcinoma of Lung", "Stage IB Non-Oat Cell Carcinoma of the Lung", "Stage IB Non-Small Cell Carcinoma of the Lung", "Stage IB Non-Small Cell Lung Carcinoma AJCC v7", "Stage IB Lung Non-Small Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Non-Small Cell Lung Carcinoma AJCC v7", "shortest_name_length": 35}
{"curie": "UMLS:C4331315", "names": ["Stage I Lip and Oral Cavity Cancer", "Stage I Lip and Oral Cavity Cancer AJCC v8", "Stage I Lip and Oral Cavity Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Lip and Oral Cavity Cancer AJCC v8", "shortest_name_length": 34}
{"curie": "UMLS:C5208000", "names": ["New onset diabetes after transplantation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "New onset diabetes after transplantation", "shortest_name_length": 40}
{"curie": "MONDO:0012109", "names": ["Hyt4", "HYT4", "hypertension, essential, susceptibility to, 4", "HYPERTENSION, ESSENTIAL, SUSCEPTIBILITY TO, 4", "hypertension, essential, susceptibility to, type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertension, essential, susceptibility to, 4", "shortest_name_length": 4}
{"curie": "UMLS:C0740914", "names": ["dust allergy", "Dust allergy", "allergy dust", "dust; allergy", "allergy; dust", "allergies dust", "ALLERGY TO DUST", "Allergy to dust", "allergy to dust", "Allergy to dust (finding)", "allergy to dust (history)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Allergy to dust", "shortest_name_length": 12}
{"curie": "MONDO:0030037", "names": ["NEDHCAS", "GPIBD22", "GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 22", "Glycosylphosphatidylinositol Biosynthesis Defect 22", "neurodevelopmental disorder with hypotonia and cerebellar atrophy, with or without seizures", "NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND CEREBELLAR ATROPHY, WITH OR WITHOUT SEIZURES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with hypotonia and cerebellar atrophy, with or without seizures", "shortest_name_length": 7}
{"curie": "MONDO:0033493", "names": ["HGF5", "GGF5", "GINGF5", "gingival fibromatosis 5", "FIBROMATOSIS, GINGIVAL, 5", "fibromatosis, gingival, 5", "FIBROMATOSIS, GINGIVAL, HEREDITARY, 5", "fibromatosis, gingival, hereditary, 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibromatosis, gingival, 5", "shortest_name_length": 4}
{"curie": "UMLS:C2983703", "names": ["Gastric Cancer by AJCC v6 Stage", "Gastric Carcinoma by AJCC v6 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Cancer by AJCC v6 Stage", "shortest_name_length": 31}
{"curie": "UMLS:C0472381", "names": ["Posterior circulation transient ischemic attack", "Posterior Circulation Transient Ischemic Attack", "Posterior circulation transient ischaemic attack", "Transient Ischemic Attack, Posterior Circulation", "transient ischemic attack of posterior circulation", "transient ischemic attack of vertebrobasilar system", "Vertebrobasilar territory transient ischemic attack", "Vertebrobasilar territory transient ischaemic attack", "Vertebrobasilar territory transient ischemic attack (disorder)", "transient ischemic attack of posterior circulation (diagnosis)", "transient ischemic attack of vertebrobasilar system (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Posterior Circulation Transient Ischemic Attack", "shortest_name_length": 47}
{"curie": "MONDO:0034041", "names": ["congenital axonal neuropathy with encephalopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital axonal neuropathy with encephalopathy", "shortest_name_length": 48}
{"curie": "MONDO:0008000", "names": ["MA", "MGR1", "MGAU", "Mgr1", "Mgau", "migraine", "migraine, resistance to", "migraine, susceptibility to", "migraine without aura, susceptibility to", "migraine with or without aura, susceptibility to, 1", "MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1", "migraine with or without aura, susceptibility to, type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "migraine with or without aura, susceptibility to, 1", "shortest_name_length": 2}
{"curie": "MONDO:0015131", "names": ["CID", "IMMUNODEFICIENCY COMBINED", "Combined immunodeficiency", "combined immunodeficiency", "combined; immunodeficiency", "immunodeficiency; combined", "Combined immunodeficiencies", "Combined immunity deficiency", "combined immunity deficiency", "combined immunodeficiency disease", "Combined immunodeficiency disease", "Combined immunodeficiency syndrome", "combined immunodeficiency syndrome", "X-linked combined immunodeficiency", "Congenital Combined Immunodeficiency", "congenital combined immunodeficiency", "Combined immunodeficiency, unspecified", "combined T and B cell immunodeficiency", "Syndrome with combined immunodeficiency", "combined T cell and B cell immunodeficiency", "Combined immunodeficiency disease (disorder)", "combined immunodeficiency disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined immunodeficiency", "shortest_name_length": 3}
{"curie": "MONDO:0006012", "names": ["Pneumonia;viral", "Viral Pneumonia", "Pneumonia viral", "PNEUMONIA VIRAL", "pneumonia viral", "viral pneumonia", "Viral pneumonia", "pneumonia; viral", "pneumonia; virus", "virus; pneumonia", "Pneumonia, viral", "viral; pneumonia", "PNEUMONIA, VIRAL", "Viral Pneumonias", "Pneumonia, Viral", "VIRAL PNEUMONITIS", "Viral pneumonitis", "Viruses pneumonia", "viral pneumonitis", "Pneumonias, Viral", "Pneumonia viral NOS", "Viral pneumonia, NOS", "PNEUMONIA, ABACTERIAL", "Viruses caused pneumonia", "Viral pneumonia (disorder)", "viral pneumonia (diagnosis)", "Viral pneumonia, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "viral pneumonia", "shortest_name_length": 15}
{"curie": "UMLS:C4521615", "names": ["Stage IB Bone Cancer", "Stage IB Bone Cancer AJCC v8", "Stage IB Appendicular Skeleton, Trunk, Skull, and Facial Bones Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Bone Cancer AJCC v8", "shortest_name_length": 20}
{"curie": "UMLS:C5418910", "names": ["Advanced Primary Malignant Central Nervous System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Primary Malignant Central Nervous System Neoplasm", "shortest_name_length": 58}
{"curie": "UMLS:C5418954", "names": ["Metastatic Fallopian Tube Serous Adenocarcinoma", "Metastatic High-Grade Fallopian Tube Serous Adenocarcinoma", "Metastatic Fallopian Tube High-Grade Serous Adenocarcinoma", "Metastatic Fallopian Tube High Grade Serous Adenocarcinoma", "Metastatic High Grade Fallopian Tube Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Fallopian Tube High Grade Serous Adenocarcinoma", "shortest_name_length": 47}
{"curie": "MONDO:0045011", "names": ["keratinization disease", "Disorder of keratinisation", "Disorder of keratinization", "disorder of keratinization", "Disorder of keratinization (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratinization disease", "shortest_name_length": 22}
{"curie": "UMLS:C4331919", "names": ["Nutritional Vitamin D Deficiency Rickets"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nutritional Vitamin D Deficiency Rickets", "shortest_name_length": 40}
{"curie": "UMLS:C5205058", "names": ["Recurrent Non-GC/ABC DLBCL", "Recurrent Diffuse Large B-Cell Lymphoma Non-GC/ABC", "Recurrent Diffuse Large B-Cell Lymphoma Activated B-Cell Type", "Recurrent Diffuse Large B-Cell Lymphoma Non-Germinal Center/Activated B-Cell Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Diffuse Large B-Cell Lymphoma Activated B-Cell Type", "shortest_name_length": 26}
{"curie": "UMLS:C5668166", "names": ["Pleural Primary Effusion Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pleural Primary Effusion Lymphoma", "shortest_name_length": 33}
{"curie": "MONDO:0019527", "names": ["UCTD", "Undifferentiated Connective Tissue Disease", "Undifferentiated connective tissue disease", "undifferentiated connective tissue disease", "undifferentiated connective tissue syndrome", "Undifferentiated connective tissue syndrome", "Undifferentiated Connective Tissue Diseases", "Undifferentiated connective tissue disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "undifferentiated connective tissue syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0740415", "names": ["Lupus Encephalitis", "SLE encephalopathy", "ENCEPHALITIS LUPUS", "Lupus encephalitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lupus encephalitis", "shortest_name_length": 18}
{"curie": "MONDO:0037002", "names": ["benign phyllodes tumor", "Benign phyllodes tumor", "Benign Phyllodes Tumor", "Fibroadenoma phyllodes", "phyllodes tumor, benign", "fibroadenoma; phyllodes", "phyllodes; fibroadenoma", "Phyllodes tumor, benign", "Benign phyllodes tumour", "tumor; phyllodes, benign", "Phyllodes tumour, benign", "phyllodes; tumor, benign", "benign phyllodes neoplasm", "Benign Phyllodes Neoplasm", "Benign cystosarcoma phyllodes", "Benign Cystosarcoma Phyllodes", "benign cystosarcoma phyllodes", "Cystosarcoma phyllodes, benign", "Cystosarcoma phyllodes; benign", "benign; Cystosarcoma phyllodes", "Benign phyllodes tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign phyllodes tumor", "shortest_name_length": 22}
{"curie": "UMLS:C4763946", "names": ["Pedestrian Injury By Road Vehicle"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pedestrian Injury By Road Vehicle", "shortest_name_length": 33}
{"curie": "UMLS:C1511255", "names": ["Borderline Fallopian Tube Mucinous Tumor", "Borderline Fallopian Tube Mucinous Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Fallopian Tube Mucinous Tumor", "shortest_name_length": 40}
{"curie": "MONDO:0015700", "names": ["terminal complement pathway deficiency", "deficiency of complement of terminal pathway", "immunodeficiency due to C5 to C9 component complement deficiency", "immunodeficiency due to a late component of complement deficiency", "immunodeficiency due to a C5 to C9 component complement deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency due to a late component of complement deficiency", "shortest_name_length": 38}
{"curie": "MONDO:0014751", "names": ["CPRF", "cleft palate, psychomotor retardation, and distinctive Facial features", "CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES", "cleft palate, psychomotor retardation, and distinctive FACIAL features", "palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome", "palatal anomalies-multiple diastemata-facial dysmorphism-developmental delay syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0009736", "names": ["NLS1", "Neu-Laxova syndrome", "Neu-Laxova syndrome 1", "NEU-LAXOVA SYNDROME 1", "PHGDH Neu-Laxova syndrome", "Neu-Laxova syndrome type 1", "Neu-Laxova syndrome caused by mutation in PHGDH", "3-Phosphoglycerate dehydrogenase deficiency, neonatal form", "3-phosphoglycerate dehydrogenase deficiency, prenatal form", "Neu-Laxova syndrome due to 3-phosphoglycerate dehydrogenase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neu-Laxova syndrome 1", "shortest_name_length": 4}
{"curie": "UMLS:C1518710", "names": ["Ovarian Dermoid Cyst with Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Dermoid Cyst with Squamous Cell Carcinoma", "shortest_name_length": 49}
{"curie": "UMLS:C4727686", "names": ["Advanced Hypopharyngeal Squamous Cell Carcinoma", "Advanced Squamous Cell Carcinoma of the Hypopharynx", "Advanced Hypopharyngeal Throat Squamous Cell Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Hypopharyngeal Squamous Cell Carcinoma", "shortest_name_length": 47}
{"curie": "UMLS:C0542028", "names": ["Hyperplasia breast", "Breast Hyperplasia", "hyperplasia breast", "Breast hyperplasia", "breast hyperplasia", "HYPERPLASIA BREAST", "breasts hyperplasia", "hyperplasia; breast", "breast hyperplasias", "breast; hyperplasia", "Breast Proliferative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast hyperplasia", "shortest_name_length": 18}
{"curie": "MONDO:0003756", "names": ["Ovarian mucinous tumor", "Ovarian Mucinous Tumor", "ovarian mucinous tumor", "mucinous tumor of ovary", "Ovarian mucinous tumour", "Mucinous Tumor of Ovary", "mucinous tumor of Ovary", "Ovarian Mucinous Neoplasm", "ovarian mucinous neoplasm", "Mucinous Neoplasm of Ovary", "mucinous neoplasm of ovary", "Mucinous Tumor of the Ovary", "mucinous tumor of the ovary", "Mucinous neoplasm of the ovary", "mucinous neoplasm of the ovary", "Mucinous Neoplasm of the Ovary", "malignant ovarian mucinous neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian mucinous neoplasm", "shortest_name_length": 22}
{"curie": "MONDO:0011458", "names": ["LCA4", "cone-rod dystrophy", "Leber congenital amaurosis 4", "Leber Congenital Amaurosis 4", "LEBER CONGENITAL AMAUROSIS 4", "retinitis pigmentosa, juvenile", "AIPL1 Leber congenital amaurosis", "Leber congenital amaurosis type 4", "CONE-ROD DYSTROPHY, AIPL1-RELATED", "Cone-Rod Dystrophy, Aipl1-Related", "cone-rod dystrophy, Aipl1-related", "amaurosis congenita of Leber, type 4", "CONE-ROD DYSTROPHY, AIPL1-RELATED (disorder)", "Retinitis Pigmentosa, Juvenile, Aipl1-Related", "retinitis pigmentosa, juvenile, Aipl1-related", "RETINITIS PIGMENTOSA, JUVENILE, AIPL1-RELATED", "Leber congenital amaurosis caused by mutation in AIPL1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leber congenital amaurosis 4", "shortest_name_length": 4}
{"curie": "UMLS:C4330601", "names": ["MGMT-Unmethylated Glioblastoma", "Unmethylated MGMT Glioblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MGMT-Unmethylated Glioblastoma", "shortest_name_length": 30}
{"curie": "MONDO:0018496", "names": ["ARX-related encephalopathy-brain malformation spectrum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ARX-related encephalopathy-brain malformation spectrum", "shortest_name_length": 54}
{"curie": "MONDO:0014017", "names": ["IDDAM", "AUTS18", "AUTS18, FORMERLY", "susceptibility to autism 18", "autism, susceptibility to, 18", "autism, susceptibility to, type 18", "AUTISM, SUSCEPTIBILITY TO, 18, FORMERLY", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISM AND MACROCEPHALY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autism, susceptibility to, 18", "shortest_name_length": 5}
{"curie": "UMLS:C3274639", "names": ["Neonatal Opiod Withdrawal Syndrome", "Neonatal Opiate Withdrawal Syndrome", "Neonatal Opioid Withdrawal Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neonatal Opiate Withdrawal Syndrome", "shortest_name_length": 34}
{"curie": "UMLS:C5419210", "names": ["Unresectable Prostate Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Prostate Carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0019082", "names": ["PEMPHIGOID", "Pemphigoid", "pemphigoid", "Pemphigoids", "pemphigoids", "Parapemphigus", "Pemphigoid, NOS", "benign pemphigus", "Old Age pemphigus", "pemphigoid bullous", "bullous pemphigoid", "Bullous Pemphigoid", "PEMPHIGOID BULLOUS", "Bullous pemphigoid", "bullous pemphigoids", "Pemphigoid, Bullous", "bullous; pemphigoid", "PEMPHIGOID, BULLOUS", "pemphigoid; bullous", "Pemphigoid (disorder)", "pemphigoid (diagnosis)", "Bullous pemphigoid NOS", "Pemphigoid, unspecified", "BP - Bullous pemphigoid", "Bullous pemphigoid (disorder)", "bullous pemphigoid (diagnosis)", "Senile dermatitis herpetiformis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bullous pemphigoid", "shortest_name_length": 10}
{"curie": "MONDO:0003689", "names": ["familial hemolytic anemia", "Neonatal hemolytic anemia", "Neonatal hemolytic anaemia", "Hereditary Hemolytic Anemia", "anemia hemolytic congenital", "ANEMIA HEMOLYTIC HEREDITARY", "hereditary hemolytic anemia", "congenital hemolytic anemia", "Congenital Hemolytic Anemia", "Congenital hemolytic anemia", "Hereditary hemolytic anemia", "Hereditary Hemolytic Anemias", "Congenital hemolytic anaemia", "Anemia, Hereditary Hemolytic", "Congenital Hemolytic Anemias", "Hemolytic anemia, congenital", "Hemolytic Anemia, Congenital", "Hemolytic Anemia, Hereditary", "hereditary hemolytic anaemia", "congenital hemolytic anaemia", "Anemia, Congenital Hemolytic", "Congenital haemolytic anemia", "Hereditary hemolytic anemias", "Anaemia;haemolytic;hereditary", "Congenital haemolytic anaemia", "hereditary haemolytic anaemia", "Anemias, Congenital Hemolytic", "Anemia, Hemolytic, Hereditary", "Hemolytic Anemias, Hereditary", "hemolytic; anemia, hereditary", "Anemia, Hemolytic, Congenital", "Anemias, Hereditary Hemolytic", "anemia; hemolytic, hereditary", "Hereditary haemolytic anaemia", "Hemolytic Anemias, Congenital", "hereditary haemolytic anaemias", "Hereditary haemolytic anaemias", "anaemias haemolytics hereditary", "Congenital hemolytic anemia NOS", "Hereditary hemolytic anemia NOS", "Congenital hemolytic anemia, NOS", "Hereditary hemolytic anemia, NOS", "Congenital haemolytic anaemia NOS", "Hereditary haemolytic anaemia NOS", "Hereditary haemolytic anaemia, NOS", "Congenital haemolytic anaemia, NOS", "Congenital hemolytic anemia (disorder)", "Hereditary hemolytic anemia (disorder)", "hereditary hemolytic anemia (diagnosis)", "anemia; congenital, hereditary hemolytic", "Hereditary hemolytic anemia, unspecified", "congenital; anemia, hereditary hemolytic", "Hereditary haemolytic anaemia, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial hemolytic anemia", "shortest_name_length": 25}
{"curie": "MONDO:0014532", "names": ["IMMD", "isolated mitochondrial myopathy", "myopathy, isolated mitochondrial, autosomal dominant", "MYOPATHY, ISOLATED MITOCHONDRIAL, AUTOSOMAL DOMINANT", "Autosomal dominant mitochondrial myopathy with exercise intolerance", "autosomal dominant mitochondrial myopathy with exercise intolerance", "Autosomal dominant mitochondrial myopathy with exercise intolerance (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant mitochondrial myopathy with exercise intolerance", "shortest_name_length": 4}
{"curie": "MONDO:0019198", "names": ["sympathetic uveitis", "Sympathetic uveitis", "Sympathetic Uveitis", "uveitis; sympathetic", "sympathetic; uveitis", "Uveitis, Sympathetic", "Sympathetic Uveitides", "sympathetic ophthalmia", "Sympathetic Ophthalmia", "Sympathetic ophthalmia", "Uveitides, Sympathetic", "Sympathetic Ophthalmias", "Ophthalmia, Sympathetic", "ophthalmia; sympathetic", "sympathetic; ophthalmia", "Ophthalmias, Sympathetic", "Sympathetic ophthalmitis", "Sympathetic uveitis (disorder)", "sympathetic uveitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sympathetic ophthalmia", "shortest_name_length": 19}
{"curie": "MONDO:0015900", "names": ["HYPOADRENALISM", "hypoadrenalism", "HYPOALDOSTERONISM", "Hypoaldosteronism", "hypoaldosteronism", "Hypoaldosteronemia", "Hypoaldosteronaemia", "Decreased aldosterone", "Aldosterone deficiency", "Aldosterone Deficiency", "rare hypoaldosteronism", "aldosterone deficiency", "hypoaldosteronism disease", "Serum aldosterone decreased", "Decreased serum aldosterone", "Low blood aldosterone level", "Aldosterone deficiency, NOS", "Mineralocorticoid Deficiency", "hypoaldosteronism (diagnosis)", "Aldosterone deficiency syndrome", "Mineralocorticoid insufficiency", "Adrenocortical insufficiency NOS", "Decreased aldosterone production", "Aldosterone deficiency (disorder)", "Decreased circulating aldosterone level", "Unspecified adrenocortical insufficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypoaldosteronism disease", "shortest_name_length": 14}
{"curie": "MONDO:0100466", "names": ["butterfly-shaped pattern dystrophy", "butterfly-shaped pigment dystrophy", "Butterfly-shaped pigment dystrophy", "Butterfly-shaped pattern dystrophy", "butterfly-shaped pigmentary macular dystrophy", "Butterfly-shaped pigmentary macular dystrophy", "Butterfly-shaped pigmentary macular dystrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "butterfly-shaped pigment dystrophy", "shortest_name_length": 34}
{"curie": "UMLS:C5419560", "names": ["Advanced Renal Pelvis and Ureter Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Renal Pelvis and Ureter Urothelial Carcinoma", "shortest_name_length": 53}
{"curie": "UMLS:C0848309", "names": ["Perennial rhinitis", "Rhinitis;perennial", "perennial rhinitis", "Rhinitis perennial", "rhinitis perennial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rhinitis perennial", "shortest_name_length": 18}
{"curie": "UMLS:C0406537", "names": ["Morbilliform Exanthem", "Exanthem, Morbilliform", "Maculopapular Exanthem", "Morbilliform Exanthems", "Exanthem, Maculopapular", "Maculopapular Exanthems", "Exanthems, Morbilliform", "Exanthems, Maculopapular", "Morbilliform Drug Reaction", "Maculopapular Drug Eruption", "Morbilliform Drug Reactions", "Reaction, Morbilliform Drug", "Maculopapular drug eruption", "Drug Reaction, Morbilliform", "Reactions, Morbilliform Drug", "Drug Eruption, Maculopapular", "Maculopapular Drug Eruptions", "Drug Reactions, Morbilliform", "Eruption, Maculopapular Drug", "Eruptions, Maculopapular Drug", "Drug Eruptions, Maculopapular", "Maculopapular drug eruption (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Morbilliform Drug Reaction", "shortest_name_length": 21}
{"curie": "MONDO:0018171", "names": ["MOGCT", "OVARIAN GERM CELL CANCER", "ovarian germ cell cancer", "Ovarian germ cell cancer", "Ovarian Germ Cell Cancer", "OVARIAN CANCER, GERM CELL", "Ovarian germ cell cancer NOS", "ovary malignant germ cell tumor", "Malignant ovarian germ cell tumor", "malignant ovarian germ cell tumor", "malignant Ovarian germ cell tumor", "Malignant Ovarian Germ Cell Tumor", "Malignant Germ Cell Tumor of Ovary", "malignant germ cell tumor of ovary", "Malignant germ cell tumor of ovary", "Malignant germ cell tumour of ovary", "Malignant Ovarian Germ Cell Neoplasm", "malignant ovarian germ cell neoplasm", "Malignant Germ Cell Neoplasm of Ovary", "malignant germ cell neoplasm of ovary", "Ovarian germ cell neoplasms malignant", "Malignant Germ Cell Tumor of the Ovary", "malignant germ cell tumor of the ovary", "Malignant Germ Cell Neoplasm of the Ovary", "malignant germ cell neoplasm of the ovary", "ovarian neoplasm malignant germ cell tumor", "Malignant germ cell tumor of ovary (disorder)", "malignant germ cell tumor of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant germ cell tumor of ovary", "shortest_name_length": 5}
{"curie": "MONDO:0007166", "names": ["Ataxia with Fasciculations", "ATAXIA WITH FASCICULATIONS", "ataxia with fasciculations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ataxia with fasciculations", "shortest_name_length": 26}
{"curie": "UMLS:C0341221", "names": ["gastric necrosis", "Gastric necrosis", "stomach; necrosis", "necrosis; stomach", "Gastric Necrotic Lesion", "Gastric necrosis (disorder)", "gastric necrosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Necrotic Lesion", "shortest_name_length": 16}
{"curie": "MONDO:0024781", "names": ["IMD102", "SASH3 deficiency", "IMMUNODEFICIENCY 102", "immunodeficiency 102"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 102", "shortest_name_length": 6}
{"curie": "UMLS:C5206804", "names": ["Advanced Papillary Renal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Papillary Renal Cell Carcinoma", "shortest_name_length": 39}
{"curie": "UMLS:C0856526", "names": ["Fredrickson Type I Lipidemia", "Fredrickson Type I lipidemia", "Fredrickson Type I lipidaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fredrickson Type I lipidaemia", "shortest_name_length": 28}
{"curie": "UMLS:C5557173", "names": ["Stage IIB Cervical Cancer AJCC v9", "Stage IIB Cervical Carcinoma AJCC v9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Cervical Cancer AJCC v9", "shortest_name_length": 33}
{"curie": "MONDO:0021320", "names": ["mouth floor cancer", "Mouth floor cancer", "cancer of mouth floor", "Cancer of floor of mouth", "CA - Cancer of floor of mouth", "malignant floor of mouth tumor", "Malignant Floor of Mouth Tumor", "malignant mouth floor neoplasm", "FOM - Cancer of floor of mouth", "malignant neoplasm of mouth floor", "malignant floor of mouth neoplasm", "Malignant Tumor of Floor of Mouth", "Malignant Floor of Mouth Neoplasm", "Malignant tumor of floor of mouth", "malignant tumor of floor of mouth", "Malignant tumour of floor of mouth", "malignant floor of the mouth tumor", "Malignant Floor of the Mouth Tumor", "Malignant neoplasm of floor of mouth", "malignant neoplasm of floor of mouth", "Malignant Neoplasm of Floor of Mouth", "Malignant Floor of the Mouth Neoplasm", "malignant floor of the mouth neoplasm", "FOM - Malignant tumor of floor of mouth", "FOM - Malignant tumour of floor of mouth", "malignant tumor of the floor of the mouth", "Malignant neoplasm of floor of mouth, NOS", "Malignant Tumor of the Floor of the Mouth", "Malignant tumor of floor of mouth (disorder)", "malignant neoplasm of the floor of the mouth", "Malignant Neoplasm of the Floor of the Mouth", "malignant neoplasm of floor of mouth (diagnosis)", "Malignant neoplasm of floor of mouth, unspecified", "Malignant neoplasm of floor of mouth, part unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant tumor of floor of mouth", "shortest_name_length": 18}
{"curie": "MONDO:0014740", "names": ["DFNA68", "autosomal dominant deafness 68", "deafness, autosomal dominant 68", "DEAFNESS, AUTOSOMAL DOMINANT 68", "deafness, autosomal dominant type 68", "autosomal dominant nonsyndromic deafness 68", "autosomal dominant nonsyndromic hearing loss 68", "HOMER2 autosomal dominant nonsyndromic deafness", "autosomal dominant nonsyndromic deafness type 68", "autosomal dominant nonsyndromic deafness caused by mutation in HOMER2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 68", "shortest_name_length": 6}
{"curie": "UMLS:C0543822", "names": ["Atherosclerotic ischemic disease", "atherosclerosis occlusive disease", "Atherosclerotic occlusive disease", "Atherosclerotic ischaemic disease", "Atherosclerotic occlusive disease (disorder)", "atherosclerosis occlusive disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atherosclerotic occlusive disease", "shortest_name_length": 32}
{"curie": "MONDO:0002812", "names": ["inner ear infection", "inner Ear infection", "infection inner ear", "Inner Ear Infection", "ear infection inner", "Inner ear infection", "infection; inner ear", "inner ear; infection", "ear infections inner", "internal Ear infection", "Internal Ear Infection", "infectious labyrinthitis", "infectious otitis interna", "Infectious Otitis Interna"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infectious otitis interna", "shortest_name_length": 19}
{"curie": "MONDO:0004682", "names": ["retromolar area cancer", "malignant tumor of retromolar area", "Malignant tumor of retromolar area", "malignant retromolar area neoplasm", "Malignant tumour of retromolar area", "malignant neoplasm of retromolar area", "Malignant neoplasm of retromolar area", "neoplasm of retromolar area, malignant", "Malignant tumor of retromolar area (disorder)", "malignant neoplasm of retromolar area (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retromolar area cancer", "shortest_name_length": 22}
{"curie": "MONDO:0018764", "names": ["microcephalic primordial dwarfism due to RTTN deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephalic primordial dwarfism due to RTTN deficiency", "shortest_name_length": 56}
{"curie": "MONDO:0020539", "names": ["extragonadal non-dysgerminomatous germ cell tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extragonadal non-dysgerminomatous germ cell tumor", "shortest_name_length": 49}
{"curie": "MONDO:0032649", "names": ["HYPT14", "hypotrichosis 14", "HYPOTRICHOSIS 14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotrichosis 14", "shortest_name_length": 6}
{"curie": "UMLS:C1336024", "names": ["Solar Radiation-Related Skin Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Solar Radiation-Related Skin Squamous Cell Carcinoma", "shortest_name_length": 52}
{"curie": "MONDO:0005667", "names": ["Biliary dyskinesia", "BILIARY DYSKINESIA", "biliary dyskinesia", "dyskinesia biliary", "Biliary Dyskinesia", "dyskinesia; biliary", "biliary; dyskinesia", "Dyskinesia, Biliary", "biliary dyskinesias", "Biliary Dyskinesias", "Dyskinesias, Biliary", "Hyperkinetic gallbladder", "sphincter of Oddi dysfunction", "sphincter of oddi dysfunction", "Biliary dyskinesia (disorder)", "biliary dyskinesia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "biliary dyskinesia", "shortest_name_length": 18}
{"curie": "MONDO:0006493", "names": ["Warthin Tumor", "Warthin tumor", "adenolymphoma", "warthin tumor", "Adenolymphoma", "Tumor, Warthin", "Adenolymphomas", "tumor warthins", "warthin's tumor", "Warthin's Tumor", "Warthin's tumor", "tumor warthin's", "tumors warthin's", "Warthin's tumour", "warthin's tumour", "Adenolymphoma (disorder)", "Salivary Gland Warthin Tumor", "papillary cystadenoma lymphomatosum", "Papillary cystadenoma lymphomatosum", "Papillary Cystadenoma Lymphomatosum", "Cystadenoma Lymphomatosum, Papillary", "Adenolymphoma (morphologic abnormality)", "papillary cystadenoma lymphomatosum (formerly)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Warthin tumor", "shortest_name_length": 13}
{"curie": "MONDO:0005425", "names": ["podoconiosis", "soil elephantiasis", "elephantiasis from soil", "nonfilarial elephantiasis", "non-filarial elephantiasis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "podoconiosis", "shortest_name_length": 12}
{"curie": "UMLS:C5670554", "names": ["Advanced Prostate Adenocarcinoma with Neuroendocrine Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Prostate Adenocarcinoma with Neuroendocrine Differentiation", "shortest_name_length": 68}
{"curie": "MONDO:0550003", "names": ["SEC61B-related polycystic liver disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SEC61B-related polycystic liver disease", "shortest_name_length": 39}
{"curie": "MONDO:0019190", "names": ["juvenile polyposis of infancy", "infantile juvenile polyposis syndrome", "juvenile polyposis syndrome of infancy", "infantile onset juvenile polyposis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile polyposis of infancy", "shortest_name_length": 29}
{"curie": "UMLS:C4285850", "names": ["Poor quality device used"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Poor quality device used", "shortest_name_length": 24}
{"curie": "UMLS:C1514920", "names": ["Retroperitoneal EGIST", "Retroperitoneal Gastrointestinal Stromal Tumor", "Retroperitoneal Extragastrointestinal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retroperitoneal Gastrointestinal Stromal Tumor", "shortest_name_length": 21}
{"curie": "UMLS:C0392702", "names": ["abnormal involuntary movement", "Abnormal involuntary movement", "involuntary movement; abnormal", "Abnormal;movements;involuntary", "Abnormal involuntary movements", "abnormal involuntary movements", "abnormal; involuntary movement", "movement; abnormal, involuntary", "Abnormal involuntary movement (disorder)", "Unspecified abnormal involuntary movements"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abnormal involuntary movement", "shortest_name_length": 29}
{"curie": "UMLS:C4524521", "names": ["Stage I", "Stage I Head and Neck Squamous Cell Cancer", "Stage I Cutaneous Squamous Cell Carcinoma of the Head and Neck AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Cutaneous Squamous Cell Carcinoma of the Head and Neck AJCC v8", "shortest_name_length": 7}
{"curie": "UMLS:C0588233", "names": ["Sepsis due to Enterococcus", "Septicemia due to enterococcus", "Septicaemia due to enterococcus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Septicemia due to enterococcus", "shortest_name_length": 26}
{"curie": "UMLS:C1518708", "names": ["Ovarian Dermoid Cyst with Secondary Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Dermoid Cyst with Secondary Sarcoma", "shortest_name_length": 43}
{"curie": "MONDO:0006926", "names": ["Hib", "Hemophilus diseases", "Hemophilus infection", "Hemophilus Infection", "hemophilus infection", "Haemophilus Infection", "infection, Hemophilus", "Hemophilus infections", "Hemophilus Infections", "Haemophilus infection", "Infection, Hemophilus", "haemophilus infection", "infections, Hemophilus", "haemophilus infections", "Infection, Haemophilus", "HAEMOPHILUS INFECTIONS", "Haemophilus Infections", "infection, Haemophilus", "Infections, Hemophilus", "Haemophilus infections", "infections, Haemophilus", "Infections, Haemophilus", "Hemophilus infection NOS", "Haemophilus infection NOS", "Haemophilus infection, NOS", "haemophilus infectious disease", "Haemophilus infectious disease", "Haemophilus disease or disorder", "Haemophilus infection (disorder)", "haemophilus infection (diagnosis)", "Haemophilus caused disease or disorder", "primary Haemophilus infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "haemophilus infectious disease", "shortest_name_length": 3}
{"curie": "MONDO:0004710", "names": ["uterus carcinoma in situ", "stage 0 uterus carcinoma", "uterus in situ carcinoma", "Cancer in situ of uterus", "Uterine carcinoma in situ", "Carcinoma in situ of uterus", "carcinoma in situ of uterus", "Carcinoma in situ of uterus, NOS", "Carcinoma in situ of uterus (disorder)", "carcinoma in situ of uterus (diagnosis)", "Carcinoma in situ of other and unspecified parts of uterus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterus carcinoma in situ", "shortest_name_length": 24}
{"curie": "MONDO:0005491", "names": ["Chagas cardiomyopathy", "Chagas Cardiomyopathy", "Chagas' cardiomyopathy", "Cardiomyopathy, Chagas", "Chagas' Cardiomyopathy", "Cardiomyopathy, Chagas'", "Cardiovascular Trypanosomiasis", "Chagas' disease cardiomyopathy", "Trypanosomiasis, Cardiovascular", "Trypanosoma cruzi cardiomyopathy", "Cardiomyopathy in Chagas' disease", "Cardiomyopathy in Chagas' Disease", "trypanosomiasis involving the heart", "Chagas' disease with heart involvement", "Chronic Chagas' Disease Cardiomyopathy", "Trypanosoma cruzi caused cardiomyopathy", "Chagas; acute, cardiovascular (etiology)", "trypanosomiasis with cardiac involvement", "Chagas; cardiovascular involvement (etiology)", "Chagas' disease with heart involvement (disorder)", "Chagas; cardiovascular involvement (manifestation)", "trypanosomiasis with cardiac involvement (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chagas cardiomyopathy", "shortest_name_length": 21}
{"curie": "MONDO:0009099", "names": ["Schofer Beetz Bohl syndrome", "Schofer-Beetz-Bohl syndrome", "nephrogenic diabetes insipidus-intracranial calcification syndrome", "Nephrogenic diabetes insipidus and intracranial calcification syndrome", "Nephrogenic diabetes insipidus and intracranial calcification syndrome (disorder)", "diabetes insipidus nephrogenic mental retardation and intracerebral calcification", "diabetes insipidus nephrogenic intellectual disability and intracerebral calcification", "Diabetes Insipidus, Nephrogenic, with Mental Retardation and Intracerebral Calcification", "DIABETES INSIPIDUS, NEPHROGENIC, WITH MENTAL RETARDATION AND INTRACEREBRAL CALCIFICATION", "diabetes insipidus, nephrogenic, with mental retardation and intracerebral calcification", "diabetes insipidus, nephrogenic, with intellectual disability and intracerebral calcification"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrogenic diabetes insipidus-intracranial calcification syndrome", "shortest_name_length": 27}
{"curie": "MONDO:0006507", "names": ["HH", "Hemosiderosis", "Hemochromatose", "Hanot-Chauffard", "diabetes bronze", "hemochromatoses", "hemochromatosis", "Bronze diabetes", "HEMOCHROMATOSIS", "bronze diabetes", "Hemochromatosis", "Bronze Diabetes", "Hemochromatoses", "Haemochromatosis", "HAEMOCHROMATOSIS", "DIABETES, BRONZE", "Diabetes, Bronze", "Bronzed diabetes", "bronzed diabetes", "Haemochromatoses", "haemochromatosis", "bronzed; diabetes", "Bronzed Cirrhosis", "Bronzed Cirrhoses", "Hematochromatosis", "diabetes; bronzed", "Cirrhosis, Bronzed", "Cirrhoses, Bronzed", "Hemochromatosis NOS", "IRON STORAGE DISEASE", "iron storage disease", "Iron storage disease", "Hemochromatosis, NOS", "Pigmentary Cirrhoses", "Pigmentary Cirrhosis", "Iron overload disease", "Cirrhoses, Pigmentary", "Cirrhosis, Pigmentary", "Iron Storage Disorder", "Iron Overload Disease", "iron storage disorder", "iron; storage disorder", "Storage Disorder, Iron", "disorders iron storage", "Iron Storage Disorders", "Disorder, Iron Storage", "Disorders, Iron Storage", "Storage Disorders, Iron", "Primary Hemochromatosis", "Genetic Hemochromatoses", "primary hemochromatosis", "PRIMARY HEMOCHROMATOSIS", "Genetic Hemochromatosis", "Primary hemochromatosis", "Familial Hemochromatosis", "Familial Hemochromatoses", "primary haemochromatosis", "familial hemochromatosis", "Familial hemochromatosis", "Hemochromatosis, Genetic", "Primary haemochromatosis", "HEMOCHROMATOSIS, PRIMARY", "Hemochromatoses, Genetic", "Familial haemochromatosis", "Iron storage disease, NOS", "Hemochromatosis, Familial", "HEMOCHROMATOSIS, FAMILIAL", "Hemochromatoses, Familial", "familial haemochromatosis", "Hemochromatosis (disorder)", "Hereditary Hemochromatosis", "hereditary hemochromatosis", "hemochromatosis hereditary", "idiopathic hemochromatosis", "Bronze diabetes (disorder)", "Hereditary hemochromatosis", "Idiopathic hemochromatosis", "hereditary haemochromatosis", "iron accumulation disorders", "bronze diabetes (diagnosis)", "Hereditary haemochromatosis", "HEMOCHROMATOSIS, HEREDITARY", "hemochromatosis (diagnosis)", "hemochromatosis, hereditary", "HEMOCHROMATOSIS, IDIOPATHIC", "Idiopathic haemochromatosis", "Hemochromatosis, unspecified", "Rare hereditary hemochromatosis", "Troisier Hanot Chauffard Syndrome", "Troisier-Hanot-Chauffard Syndrome", "TROISIER-HANOT-CHAUFFARD SYNDROME", "Syndrome, Troisier-Hanot-Chauffard", "Troisier-Hanot-Chauffard Syndromes", "Primary hemochromatosis (disorder)", "Von Recklenhausen-Applebaum Disease", "primary hemochromatosis (diagnosis)", "Von Recklenhausen Applebaum Disease", "Syndromes, Troisier-Hanot-Chauffard", "von Recklinghausen-Appelbaum disease", "Recklenhausen-Applebaum Disease, Von", "Von Recklenhausen-Applebaum Diseases", "Disease, Von Recklenhausen-Applebaum", "von Recklinghausen-Applebaum disease", "Recklenhausen-Applebaum Diseases, Von", "Hereditary hemochromatosis (disorder)", "Diseases, Von Recklenhausen-Applebaum", "Idiopathic hemochromatosis (disorder)", "Hereditary hemochromatosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary hemochromatosis", "shortest_name_length": 2}
{"curie": "UMLS:C0231926", "names": ["Ventilatory defect", "Ventilatory defect, NOS", "Ventilatory defect (finding)", "RESP GAS EXCHANGE DISORDER NOS", "Resp gas exchange disorder NOS", "Respiratory gas exchange disorder", "Respiratory gas exchange disorder NOS", "Respiratory gas exchange disorder, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ventilatory defect", "shortest_name_length": 18}
{"curie": "UMLS:C0694571", "names": ["lymphoma extranodal", "extranodal lymphoma", "Extranodal Lymphoma", "extranodal lymphomas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extranodal Lymphoma", "shortest_name_length": 19}
{"curie": "MONDO:0014938", "names": ["AN3", "aniridia 3", "ANIRIDIA 3", "aniridia type 3", "aniridia 3; AN3", "TRIM44 isolated aniridia", "isolated aniridia caused by mutation in TRIM44"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aniridia 3", "shortest_name_length": 3}
{"curie": "MONDO:0044919", "names": ["renal pelvis cancer", "cancer of renal pelvis", "malignant renal pelvis tumor", "Malignant Renal Pelvis Tumor", "malignant tumor of renal pelvis", "Malignant Tumor of Renal Pelvis", "Malignant Renal Pelvis Neoplasm", "malignant renal pelvis neoplasm", "malignant neoplasm of renal pelvis", "Malignant Neoplasm of Renal Pelvis", "malignant tumor of the renal pelvis", "Malignant Tumor of the Renal Pelvis", "Malignant Neoplasm of the Renal Pelvis", "malignant neoplasm of the renal pelvis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant renal pelvis neoplasm", "shortest_name_length": 19}
{"curie": "UMLS:C1696082", "names": ["Peritoneal necrosis", "Peritoneal Necrotic Lesion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peritoneal Necrotic Lesion", "shortest_name_length": 19}
{"curie": "UMLS:C1332499", "names": ["Benign Extraskeletal Cartilaginous and Osseous Tumor", "Benign Extraskeletal Cartilaginous and Osseous Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Extraskeletal Cartilaginous and Osseous Neoplasm", "shortest_name_length": 52}
{"curie": "UMLS:C1515567", "names": ["Chronic Lymphoblastic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic Lymphoblastic Lymphoma", "shortest_name_length": 30}
{"curie": "UMLS:C0279589", "names": ["L1 adult ALL", "ALL, adult L1", "adult ALL, L1", "ALL, L1 adult", "L1 Acute Lymphoblastic Leukemia", "L1 adult acute lymphocytic leukemia", "L1 lymphocytic leukemia, acute adult", "L1 acute lymphocytic leukemia, adult", "acute lymphocytic leukemia, adult L1", "adult acute lymphocytic leukemia, L1", "Adult L1 Acute Lymphoblastic Leukemia", "L1 adult acute lymphoblastic leukemia", "L1 acute lymphoblastic leukemia, adult", "acute lymphoblastic leukemia, adult L1", "leukemia, adult acute lymphocytic , L1", "adult acute lymphoblastic leukemia, L1", "L1 lymphoblastic leukemia, acute adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult L1 Acute Lymphoblastic Leukemia", "shortest_name_length": 12}
{"curie": "UMLS:C1880017", "names": ["Central Nervous System Carcinoma", "Primary Central Nervous System Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Carcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C5206771", "names": ["Refractory Atypical Teratoid/Rhabdoid Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Atypical Teratoid/Rhabdoid Tumor", "shortest_name_length": 43}
{"curie": "MONDO:0017286", "names": ["TEMPI Syndrome", "TEMPI syndrome", "tempi syndrome", "telangiectasia - erythrocytosis - monoclonal gammopathy - perinephric-fluid collections - intrapulmonary shunting", "Telangiectasia-erythrocytosis-monoclonal gammopathy-perinephric-fluid collections-intrapulmonary shunting syndrome", "telangiectasia-erythrocytosis-monoclonal gammopathy-perinephric-fluid collections-intrapulmonary shunting syndrome", "Telangiectasia, erythrocytosis, monoclonal gammopathy, perinephric fluid collections and intrapulmonary shunting syndrome", "Telangiectasia, erythrocytosis, monoclonal gammopathy, perinephric fluid collections and intrapulmonary shunting syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tempi syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0700098", "names": ["neoplasm, non-human animal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplasm, non-human animal", "shortest_name_length": 26}
{"curie": "MONDO:0007143", "names": ["aortic arch anomaly with peculiar facies and mental retardation", "AORTIC ARCH ANOMALY WITH PECULIAR FACIES AND MENTAL RETARDATION", "Aortic arch anomaly with peculiar facies and mental retardation", "aortic arch anomaly - peculiar facies - intellectual disability", "aortic arch anomaly with peculiar facies and intellectual disability", "aortic arch anomaly-peculiar facies-intellectual disability syndrome", "aortic arch anomaly-facial dysmorphism-intellectual disability syndrome", "familial syndrome of right-sided aortic arch, mental deficiency, and facial dysmorphism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic arch anomaly-facial dysmorphism-intellectual disability syndrome", "shortest_name_length": 63}
{"curie": "MONDO:0009564", "names": ["MWS", "Mws", "MWKS", "Marden-Walker syndrome", "marden-walker syndrome", "marden walker syndrome", "MARDEN-WALKER syndrome", "MARDEN-WALKER SYNDROME", "Marden Walker syndrome", "Marden-Walker syndrome (MWS)", "Marden Walker syndrome (disorder)", "Generalized connective tissue syndrome", "connective tissue disorder Marden Walker type", "Connective Tissue Disorder, Marden-Walker Type", "Blepharophimosis, micrognathia, immobile facies, kyphoscoliosis, limb contractures, pigeon breast, and arachnodactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Marden-Walker syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C4552930", "names": ["Stage II Adrenal Cortex Cancer", "stage II adrenocortical cancer", "stage II adrenal cortex carcinoma", "stage II adrenocortical carcinoma", "adrenocortical carcinoma, stage II", "carcinoma, adrenocortical stage II", "Stage II Adrenal Cortex Carcinoma AJCC v8", "stage II adrenal cortex carcinoma AJCC v8", "Stage II Adrenal Cortical Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Adrenal Cortex Carcinoma AJCC v8", "shortest_name_length": 30}
{"curie": "MONDO:0001046", "names": ["Aproctia", "anus absent", "Atresia ani", "Absent anus", "absent anus", "atresia ani", "Anus absent", "anus; absent", "anus atresia", "ANAL ATRESIA", "anal atresia", "Anal atresia", "Atresia;anal", "Anal Atresia", "Atresia, Anal", "anus; atresia", "Anal Atresias", "atresia; anus", "anal stenosis", "Atresias, Anal", "imperforate anu", "Atresia of anus", "anus imperforate", "Anus imperforate", "Imperforate anus", "IMPERFORATE ANUS", "Imperforate Anus", "imperforate anus", "ANUS IMPERFORATE", "Anus, Imperforate", "anus, imperforate", "anus; imperforate", "imperforate; anus", "ANUS, IMPERFORATE", "anus imperforated", "ANAL IMPERFORATION", "the anus was absent", "Anus absent (finding)", "anorectal malformations", "Congenital anal atresia", "Anal atresia (disorder)", "the anus was imperforate", "congenital atresia of anus", "Congenital atresia of anus", "Congenital imperforate anus", "imperforate anus (diagnosis)", "absent anus (physical finding)", "imperforate anus (physical finding)", "congenital or infantile occlusion of anus", "Congenital or infantile occlusion of anus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "imperforate anus", "shortest_name_length": 8}
{"curie": "MONDO:0000090", "names": ["progressive external ophthalmoplegia with mtDNA deletions", "progressive external ophthalmoplegia with mitochondrial DNA deletions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive external ophthalmoplegia with mitochondrial DNA deletions", "shortest_name_length": 57}
{"curie": "UMLS:C0280146", "names": ["Stage II Grade 3 Follicular Lymphoma", "stage II grade 3 follicular lymphoma", "Grade III Follicular Lymphoma Stage II", "Follicular Lymphoma Grade III Stage II", "Grade III Stage II Follicular Lymphoma", "stage II follicular large cell lymphoma", "Follicular Large Cell Lymphoma Stage II", "Stage II Follicular Large Cell Lymphoma", "follicular large cell lymphoma, stage II", "Ann Arbor Stage II Grade 3 Follicular Lymphoma", "stage II grade III follicular large cell lymphoma", "Stage II Grade III Follicular Large Cell Lymphoma", "Grade III Stage II Follicular Large Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage II Grade 3 Follicular Lymphoma", "shortest_name_length": 36}
{"curie": "MONDO:0001632", "names": ["intracranial arteriosclerosis", "Intracranial Arterioscleroses", "Intracranial Arteriosclerosis", "Arteriosclerosis, Intracranial", "Arterioscleroses, Intracranial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intracranial arteriosclerosis", "shortest_name_length": 29}
{"curie": "MONDO:0006464", "names": ["Thyroid MALT Lymphoma", "thyroid MALT lymphoma", "thyroid mucosa-associated lymphoid tissue lymphoma", "Thyroid Mucosa-Associated Lymphoid Tissue Lymphoma", "Thyroid Gland Mucosa-Associated Lymphoid Tissue Lymphoma", "thyroid gland mucosa-associated lymphoid tissue lymphoma", "mucosa-associated lymphoid tissue (MALT) lymphoma of thyroid", "mucosa-associated lymphoid tissue (MALT) lymphoma of thyroid (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid gland mucosa-associated lymphoid tissue lymphoma", "shortest_name_length": 21}
{"curie": "MONDO:0018737", "names": ["CAPS", "caps", "Catastrophic APS", "catastrophic APS", "Asherson's syndrome", "Catastrophic antiphospholipid syndrome", "catastrophic antiphospholipid syndrome", "Catastrophic antiphospholipid syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "catastrophic antiphospholipid syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0019203", "names": ["AIP", "pneumonia atypical", "atypical pneumonia", "Hamman Rich Disease", "Hamman-Rich Disease", "Hamman-Rich disease", "atypical pneumonias", "Hamman-rich disease", "hamman rich syndrome", "Hamman-Rich syndrome", "hamman-rich syndrome", "Hamman-Rich Syndrome", "atypicals pneumonias", "hamman-Rich syndrome", "Hamman Rich syndrome", "Fibrosing alveolitis", "Hamman-rich syndrome", "Hamman Rich Syndrome", "Atypical bronchopneumonia", "atypical bronchopneumonia", "primary atypical pneumonia", "Primary atypical pneumonia", "Acute Interstitial Pneumonia", "Acute interstitial pneumonia", "acute interstitial pneumonia", "Pneumonia, Acute Interstitial", "Interstitial Pneumonia, Acute", "Acute Interstitial Pneumonias", "Atypical bronchopneumonia, NOS", "pneumonitis acute interstitial", "Acute interstitial pneumonitis", "Acute Interstitial Pneumonitis", "Usual interstitial pneumonitis", "acute interstitial pneumonitis", "atypical interstitial pneumonia", "Idiopathic fibrosing alveolitis", "Interstitial Pneumonitis, Acute", "idiopathic fibrosing alveolitis", "Pneumonitis, Acute Interstitial", "Primary atypical pneumonia, NOS", "Atypical interstitial pneumonia", "IDIOPATHIC FIBROSING ALVEOLITIS", "Acute Interstitial Pneumonitides", "Idiopathic interstitial pneumonia", "accelerated interstitial pneumonia", "Acute interstitial pneumonitis, NOS", "Atypical interstitial pneumonia, NOS", "UIP - Usual interstitial pneumonitis", "Diffuse idiopathic pulmonary fibrosis", "Primary atypical interstitial pneumonia", "pneumonia primary atypical interstitial", "Diffuse interstitial pulmonary fibrosis", "Acute interstitial pneumonia (disorder)", "FIBROSIS, PULMONARY, INTERSTITIAL DIFFUSE", "Acute interstitial pneumonitis (diagnosis)", "idiopathic fibrosing alveolitis (diagnosis)", "Primary atypical interstitial pneumonia, NOS", "DIPF - Diffuse interstitial pulmonary fibrosis", "idiopathic pulmonary fibrosis, acute fatal form", "Idiopathic pulmonary fibrosis, acute fatal form", "Idiopathic interstitial fibrosis of lung syndrome", "Idiopathic fibrosing alveolitis, acute fatal form", "Diffuse interstitial pulmonary fibrosis (disorder)", "Primary atypical interstitial pneumonia (disorder)", "Primary atypical interstitial pneumonia (diagnosis)", "Diffuse interstitial pulmonary fibrosis (diagnosis)", "interstitial pulmonary diseases with fibrosis diffuse"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute interstitial pneumonia", "shortest_name_length": 3}
{"curie": "MONDO:0015850", "names": ["transverse vaginal septum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transverse vaginal septum", "shortest_name_length": 25}
{"curie": "UMLS:C0879537", "names": ["irreversible toxicity", "Irreversible Toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Irreversible Toxicity", "shortest_name_length": 21}
{"curie": "MONDO:0004242", "names": ["gi bleed", "GI Bleed", "GI bleed", "gi bleeding", "GI bleeding", "GI Bleeding", "gastrostaxis", "gi hemorrhage", "GI HEMORRHAGE", "GI hemorrhage", "GI tract bleed", "GI haemorrhage", "GI HAEMORRHAGE", "GI bleeding, NOS", "GI hemorrhage, NOS", "GI haemorrhage, NOS", "gastrointestinal bleed", "Gastrointestinal bleed", "GASTROINTESTINAL BLEED", "Gastrointestinal Bleed", "Gastro intestinal bleed", "BLEEDING GASTROINTESTINAL", "GASTROINTESTINAL BLEEDING", "Bleeding;gastrointestinal", "Gastrointestinal Bleeding", "gastrointestinal bleeding", "Gastrointestinal bleeding", "Bleeding gastrointestinal", "Bleeding, Gastrointestinal", "Gastro intestinal bleeding", "gastro intestinal bleeding", "Hemorrhage gastrointestinal", "Gastrointestinal hemorrhage", "Gastrointestinal Hemorrhage", "gastrointestinal hemorrhage", "HEMORRHAGE GASTROINTESTINAL", "active peptic ulcer disease", "GASTROINTESTINAL HEMORRHAGE", "GI - Gastrointestinal bleed", "gastrointestinal haemorrhage", "Hemorrhage, Gastrointestinal", "Gastrointestinal Hemorrhages", "Gastrointestinal haemorrhage", "gastrointestinal hemorrhages", "Haemorrhage gastrointestinal", "gastrointestinal; hemorrhage", "hemorrhage; gastrointestinal", "Gastrointestinal hemorrhages", "Gastrointestinal haemorrhages", "Hemorrhage of digestive tract", "Gastro-intestinal tract bleed", "Gastrointestinal bleeding, NOS", "Haemorrhage of digestive tract", "Gastrointestinal hemorrhage NOS", "GIB - Gastrointestinal bleeding", "Gastrointestinal hemorrhage, NOS", "GASTROINTESTINAL TRACT BLEED NOS", "Gastrointestinal haemorrhage NOS", "Gastrointestinal tract bleed NOS", "GI - Gastrointestinal hemorrhage", "Gastrointestinal tract hemorrhage", "GIH - Gastrointestinal hemorrhage", "Gastrointestinal haemorrhage, NOS", "GI - Gastrointestinal haemorrhage", "hemorrhage; gastrointestinal tract", "GIH - Gastrointestinal haemorrhage", "GASTROINTESTINAL TRACT BLEED (NOS)", "gastrointestinal tract; hemorrhage", "Hemorrhage of gastrointestinal tract", "gastrointestinal bleeding (diagnosis)", "Gastrointestinal hemorrhage (disorder)", "GIT - Gastrointestinal tract hemorrhage", "GIT - Gastrointestinal tract haemorrhage", "Gastrointestinal hemorrhage, unspecified", "Gastrointestinal haemorrhage, unspecified", "Hemorrhage of gastrointestinal tract, unspecified", "Haemorrhage of gastrointestinal tract, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "active peptic ulcer disease", "shortest_name_length": 8}
{"curie": "MONDO:0009355", "names": ["Hooft disease", "HOOFT DISEASE", "Hooft syndrome", "Hooft's syndrome", "Hypolipidemia syndrome", "Hypolipidaemia syndrome", "Hooft's syndrome (disorder)", "Hypolipemia-tryptophan abnormality", "Hypolipaemia-tryptophan abnormality", "delayed physical development, erythematosquamous eruption, opaque leukonychia, intellectual disability, and low serum lipids"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hooft disease", "shortest_name_length": 13}
{"curie": "UMLS:C0347235", "names": ["Benign Supraglottic Tumor", "Benign Supraglottis Tumor", "Benign Supraglottic Neoplasm", "Benign Supraglottis Neoplasm", "Benign tumor of supraglottis", "Benign Tumor of Supraglottis", "Benign tumour of supraglottis", "Benign neoplasm of supraglottis", "Benign Neoplasm of Supraglottis", "benign neoplasm of supraglottis", "Benign Tumor of the Supraglottis", "Benign Neoplasm of the Supraglottis", "Benign neoplasm of supraglottis (disorder)", "benign neoplasm of supraglottis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign neoplasm of supraglottis", "shortest_name_length": 25}
{"curie": "UMLS:C5421298", "names": ["Nasopharyngeal Adenoid Cystic Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasopharyngeal Adenoid Cystic Carcinoma", "shortest_name_length": 39}
{"curie": "MONDO:0002887", "names": ["Bile Duct Disease", "BILE DUCT DISEASE", "bile duct disease", "Disease, Bile Duct", "Bile Duct Disorder", "bile duct disorder", "bile duct diseases", "Bile Duct Diseases", "Duct Disease, Bile", "Bile duct disorders", "Diseases, Bile Duct", "bile diseases ducts", "Duct Diseases, Bile", "bile duct disorders", "Disease of bile duct", "Bile ducts--Diseases", "biles diseases ducts", "disease of bile duct", "disorder of bile duct", "Disorder of bile duct", "bile duct disease or disorder", "Disorder of bile duct (disorder)", "disease or disorder of bile duct", "disorder of bile duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bile duct disorder", "shortest_name_length": 17}
{"curie": "MONDO:0017491", "names": ["tibial hemimelia, bilateral", "tibial longitudinal meromelia, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tibial hemimelia, bilateral", "shortest_name_length": 27}
{"curie": "UMLS:C5205961", "names": ["Seminal Vesicle Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Seminal Vesicle Squamous Cell Carcinoma", "shortest_name_length": 39}
{"curie": "MONDO:0004447", "names": ["Pituitary Stalk Meningioma", "pituitary stalk meningioma", "meningioma of pituitary stalk", "Meningioma of Pituitary Stalk", "meningioma of the pituitary stalk", "meningioma of the Pituitary Stalk", "Meningioma of the Pituitary Stalk", "pituitary stalk meningioma (disease)", "meningioma (disease) of pituitary stalk"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pituitary stalk meningioma", "shortest_name_length": 26}
{"curie": "DOID:0080623", "names": ["PBD1C", "HMLR1", "Heimler syndrome", "Heimler syndrome 1", "HEIMLER SYNDROME 1", "PEROXISOME BIOGENESIS DISORDER 1C", "peroxisomal biogenesis disorder 1C", "Deafness enamel hypoplasia nail defects", "Deafness-enamel hypoplasia-nail defects syndrome", "Deafness, enamel hypoplasia, nail defect syndrome", "Hearing loss-enamel hypoplasia-nail defects syndrome", "Deafness, enamel hypoplasia, nail defect syndrome (disorder)", "HEARING LOSS, SENSORINEURAL, WITH ENAMEL HYPOPLASIA AND NAIL DEFECTS", "Hearing Loss, Sensorineural, With Enamel Hypoplasia And Nail Defects", "Sensorineural hearing loss, enamel hypoplasia, and nail abnormalities", "Bilateral sensorineural hearing loss, enamel hypoplasia and nail defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Heimler syndrome 1", "shortest_name_length": 5}
{"curie": "UMLS:C2887097", "names": ["Sepsis due to Serratia", "Sepsis caused by Serratia", "Sepsis caused by Serratia (disorder)", "Severe sepsis with acute organ dysfunction caused by Serratia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sepsis caused by Serratia", "shortest_name_length": 22}
{"curie": "MONDO:0002756", "names": ["chest wall plasmacytoma", "plasmacytoma of chest wall", "Chest Wall Solitary Plasmacytoma", "chest wall solitary plasmacytoma", "solitary plasmacytoma of chest wall", "Solitary Plasmacytoma of Chest Wall", "Solitary Plasmacytoma of the Chest Wall", "Solitary plasmacytoma of the Chest Wall", "solitary plasmacytoma of the chest wall"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "solitary plasmacytoma of chest wall", "shortest_name_length": 23}
{"curie": "MONDO:0021024", "names": ["MALARIA, RESISTANCE TO", "malaria, resistance to", "malaria, susceptibility to", "MALARIA, SUSCEPTIBILITY TO", "malaria, protection against", "malaria, Severe, resistance to", "MALARIA, SEVERE, RESISTANCE TO", "malaria, cerebral, resistance to", "MALARIA, CEREBRAL, RESISTANCE TO", "malaria, Severe, susceptibility to", "malaria, cerebral, reduced risk of", "malaria, vivax, protection against", "MALARIA, SEVERE, SUSCEPTIBILITY TO", "malaria, cerebral, susceptibility to", "MALARIA, CEREBRAL, SUSCEPTIBILITY TO", "resistance to malaria due to G6PD deficiency", "MALARIA, CEREBRAL, SUSCEPTIBILITY TO (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malaria, susceptibility to", "shortest_name_length": 22}
{"curie": "MONDO:0018585", "names": ["pediatric AIS", "childhood AIS", "pediatric arterial ischemic stroke", "childhood arterial ischemic stroke"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pediatric arterial ischemic stroke", "shortest_name_length": 13}
{"curie": "UMLS:C2981637", "names": ["Stage IVA Hilar Cholangiocarcinoma", "Stage IVA Hilar Cholangiocarcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Hilar Cholangiocarcinoma AJCC v7", "shortest_name_length": 34}
{"curie": "UMLS:C3897082", "names": ["Stage IVA Colon Cancer", "Stage IVA Colon Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Colon Cancer AJCC v7", "shortest_name_length": 22}
{"curie": "UMLS:C4552013", "names": ["Stage IIA Cervical Cancer", "Stage IIA Cervical Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Cervical Cancer AJCC v7", "shortest_name_length": 25}
{"curie": "MONDO:0021075", "names": ["Neoplastic Polyp", "neoplastic polyp"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplastic polyp", "shortest_name_length": 16}
{"curie": "MONDO:0023098", "names": ["Char douglas Dungan syndrome", "extrasystoles short stature hyperpigmentation microcephaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extrasystoles short stature hyperpigmentation microcephaly", "shortest_name_length": 28}
{"curie": "UMLS:C4551548", "names": ["Anaplastic Astrocytoma", "Grade 3 Pediatric Astrocytoma", "Grade 3 Childhood Astrocytoma", "grade III childhood astrocytoma", "Grade III Pediatric Astrocytoma", "grade III pediatric astrocytoma", "Grade III Childhood Astrocytoma", "Anaplastic Childhood Astrocytoma", "Anaplastic Pediatric Astrocytoma", "Childhood Anaplastic Astrocytoma", "anaplastic pediatric astrocytoma", "anaplastic childhood astrocytoma", "astrocytoma, grade III childhood", "childhood anaplastic astrocytoma", "Grade 3 Pediatric Astrocytic Tumor", "Grade 3 Childhood Astrocytic Tumor", "grade III pediatric astrocytic tumor", "grade III childhood astrocytic tumor", "Grade III Childhood Astrocytic Tumor", "Grade III Pediatric Astrocytic Tumor", "Grade 3 Pediatric Astrocytic Neoplasm", "Grade 3 Childhood Astrocytic Neoplasm", "Undifferentiated Pediatric Astrocytoma", "undifferentiated pediatric astrocytoma", "Undifferentiated Childhood Astrocytoma", "undifferentiated childhood astrocytoma", "Grade III Pediatric Astrocytic Neoplasm", "Grade III Childhood Astrocytic Neoplasm", "grade III childhood astrocytic neoplasm", "grade III pediatric astrocytic neoplasm", "grade III childhood cerebral astrocytoma", "CNS tumor, childhood grade III astrocytoma", "CNS tumor, grade III childhood astrocytoma", "brain tumor, childhood grade III astrocytoma", "childhood brain tumor, grade III astrocytoma", "grade III childhood supratentorial astrocytoma", "childhood CNS tumor, childhood grade III astrocytoma", "central nervous system tumor, astrocytoma, grade III childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade III Childhood Astrocytoma", "shortest_name_length": 22}
{"curie": "MONDO:0018592", "names": ["Cutaneous PAN", "cutaneous PAN", "Nodular livedo", "Cutaneous livedo with nodules", "cutaneous polyarteritis nodosa", "Cutaneous Polyarteritis Nodosa", "cutaneous periarteritis nodosa", "Cutaneous polyarteritis nodosa", "Cutaneous periarteritis nodosa", "Cutaneous polyarteritis nodosa (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous polyarteritis nodosa", "shortest_name_length": 13}
{"curie": "MONDO:0005292", "names": ["COLITIS", "colitis", "Colitis", "Colitides", "Colitis NOS", "Colitis, NOS", "COLITIS (NOS)", "Colitis (NOS)", "Colon inflamed", "colitis (disease)", "Colitis (disorder)", "colon inflammation", "Colon inflammation", "colitis (diagnosis)", "inflammation of colon", "Inflammation of colon", "COLON NOS INFLAMMATION", "Ileocecal valve inflammation", "Ileocaecal valve inflammation", "colon (non-specific) inflammation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colitis", "shortest_name_length": 7}
{"curie": "UMLS:C0016429", "names": ["follicular ovary cyst", "ovary follicular cyst", "Cyst;follicular;ovary", "cyst follicular ovary", "Follicle Cyst of Ovary", "Graafian follicle cyst", "graafian follicle; cyst", "GRAAFIAN FOLLICLE, CYST", "ovarian follicular cyst", "OVARIAN CYST FOLLICULAR", "follicular ovarian cyst", "cyst; graafian follicle", "cysts follicular ovarian", "Follicular cyst of ovary", "cysts follicular ovaries", "follicular cyst of ovary", "Follicular Cyst of Ovary", "Cyst of graafian follicle", "Follicular cystic ovary disease", "Follicular cyst of ovary (disorder)", "follicular cyst of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Follicular cyst of ovary", "shortest_name_length": 21}
{"curie": "MONDO:0007466", "names": ["HS3", "D1Z1", "DNA, satellite, 3", "DNA, SATELLITE, III", "DNA, satellite, III", "DNA, satellite, type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DNA, satellite, 3", "shortest_name_length": 3}
{"curie": "UMLS:C4552686", "names": ["IA", "Stage IA Cervical Cancer", "Stage IA Cervical Cancer AJCC v8", "Stage IA Cervical Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Cervical Cancer AJCC v8", "shortest_name_length": 2}
{"curie": "UMLS:C0333977", "names": ["Atypical hyperplasia", "hyperplasia atypical", "atypical hyperplasia", "Atypical Hyperplasia", "Atypical hyperplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypical hyperplasia", "shortest_name_length": 20}
{"curie": "MONDO:0014004", "names": ["IBGC4", "BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 4", "basal ganglia calcification, idiopathic, 4", "basal ganglia calcification, idiopathic, type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "basal ganglia calcification, idiopathic, 4", "shortest_name_length": 5}
{"curie": "UMLS:C5237720", "names": ["Oligometastatic Gastric Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oligometastatic Gastric Adenocarcinoma", "shortest_name_length": 38}
{"curie": "UMLS:C0418370", "names": ["Assault By Firearm", "Assault by firearms", "Assault by firearms (event)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Assault by firearms", "shortest_name_length": 18}
{"curie": "MONDO:0004681", "names": ["learning disorder", "Disorder;learning", "Learning Disorder", "Learning disorder", "disorder; learning", "Learning disorders", "learning disorders", "learning; disorder", "Disorder, Learning", "Learning Disorders", "disability learning", "learning disability", "LEARNING DISABILITY", "Learning Disability", "Disorders, Learning", "Learning disability", "Learning differences", "Disability, Learning", "Learning Disabilities", "learning disabilities", "Learning disorder NOS", "Learning disabilities", "disabilities learning", "Learning disorder, NOS", "Disabilities, Learning", "Academic skill disorder", "Learning disability NOS", "academic skills disorder", "Basic learning disability", "General learning disability", "Academic skill disorder, NOS", "Developmental Academic Disorder", "developmental academic disorder", "Developmental academic disorder", "Developmental Academic Disorders", "Academic Disorder, Developmental", "Academic Disorders, Developmental", "Developmental Academic Disability", "Academic Disability, Developmental", "Disability, Developmental Academic", "Developmental Academic Disabilities", "Academic Disabilities, Developmental", "Disabilities, Developmental Academic", "Developmental academic disorder, NOS", "learning disability (physical finding)", "Scholastic Skills Development Disorders", "developmental scholastic skills disorder", "developmental disorder; scholastic skills", "scholastic skills; developmental disorder", "Developmental disorder of scholastic skill", "Developmental academic disorder (disorder)", "Developmental disorder of scholastic skills", "Developmental Disorders of Scholastic Skills", "Developmental Disabilities of Scholastic Skills", "developmental scholastic skills disorder (diagnosis)", "Developmental disorder of scholastic skills, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "learning disability", "shortest_name_length": 17}
{"curie": "MONDO:0016419", "names": ["Familial breast cancer", "familial breast cancer", "breast cancer, somatic", "breast cancer, familial", "Breast Cancer, Familial", "BREAST CANCER, FAMILIAL", "Hereditary Breast Cancer", "hereditary breast cancer", "Hereditary breast cancer", "familial cancer of breast", "familial breast carcinoma", "Familial breast carcinoma", "Familial Cancer of Breast", "Familial Breast Carcinoma", "Familial cancer of breast", "Hereditary breast carcinoma", "familial breast cancer male", "Hereditary Breast Carcinoma", "hereditary breast carcinoma", "breast cancer, familial Male", "familial breast cancer, male", "Breast Cancer, Familial Male", "BREAST CANCER, FAMILIAL MALE", "familial cancer of the breast", "Familial Cancer of the Breast", "breast cancer, lobular, somatic", "familial breast cancer (diagnosis)", "Familial cancer of breast (disorder)", "familial breast cancer, male (diagnosis)", "breast cancer susceptibility, autosomal dominant, somatic mutation", "breast cancer, invasive ductal, autosomal dominant, somatic mutation", "breast cancer, susceptibility to, autosomal dominant, somatic mutation", "breast cancer, protection against, autosomal dominant, somatic mutation", "breast cancer, male, susceptibility to, autosomal dominant, somatic mutation", "breast cancer, early-onset, susceptibility to, autosomal dominant, somatic mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary breast carcinoma", "shortest_name_length": 22}
{"curie": "MONDO:0003334", "names": ["Demyelinating neuropathy", "neuropathy demyelinating", "NEUROPATHY DEMYELINATING", "demyelinating neuropathy", "demyelinating neuropathies", "demyelinated polyneuropathy", "demyelinating polyneuropathy", "POLYNEUROPATHY DEMYELINATING", "polyneuropathy demyelinating", "Demyelinating Polyneuropathy", "Demyelinating polyneuropathy", "Demyelinating neuropathy, NOS", "demyelinating polyneuropathies", "Demyelinating polyneuropathy NOS", "Demyelinating polyneuropathy, NOS", "Demyelinating peripheral neuropathy", "peripheral demyelinating neuropathy", "Peripheral demyelinating neuropathy", "Peripheral demyelinating neuropathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "demyelinating polyneuropathy", "shortest_name_length": 24}
{"curie": "UMLS:C0752135", "names": ["Anatomical Pathological Condition", "Pathological Condition, Anatomical", "Condition, Anatomical Pathological", "Anatomical Pathological Conditions", "Pathological Conditions, Anatomical", "Conditions, Anatomical Pathological"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathological Conditions, Anatomical", "shortest_name_length": 33}
{"curie": "MONDO:0020849", "names": ["IMD57", "IMMUNODEFICIENCY 57", "immunodeficiency 57", "immunodeficiency 57 with autoinflammation", "IMMUNODEFICIENCY 57 WITH AUTOINFLAMMATION", "immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections-lymphopenia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 57", "shortest_name_length": 5}
{"curie": "MONDO:0009831", "names": ["pancreas cancer", "pancreatic tumor", "pancreas neoplasm", "pancreatic cancer", "cancer of pancreas", "Ca head of pancreas", "Ca body of pancreas", "Ca tail of pancreas", "pancreatic neoplasm", "Cancer of head of pancreas", "malignant pancreas neoplasm", "Malignant Pancreatic Neoplasm", "malignant pancreatic neoplasm", "PANCREAS HEAD CANCER MALIGNANT", "malignant neoplasm of pancreas", "Malignant Neoplasm of Pancreas", "pancreatic neoplasm malignant body", "pancreatic neoplasm malignant head", "malignant neoplasm of the pancreas", "pancreatic neoplasm malignant tail", "Malignant Neoplasm of the Pancreas", "Malignant tumor of head of pancreas", "Malignant tumor of body of pancreas", "Malignant tumor of tail of pancreas", "Malignant tumour of head of pancreas", "Malignant tumour of tail of pancreas", "Malignant tumour of body of pancreas", "Malignant neoplasm of pancreatic tail", "Malignant neoplasm of tail of pancreas", "Malignant neoplasm of head of pancreas", "Malignant neoplasm of body of pancreas", "malignant neoplasm of head of pancreas", "malignant neoplasm of tail of pancreas", "malignant neoplasm of body of pancreas", "Malignant tumor of head of pancreas (disorder)", "Malignant tumor of tail of pancreas (disorder)", "Malignant tumor of body of pancreas (disorder)", "malignant neoplasm of head of pancreas (diagnosis)", "malignant neoplasm of tail of pancreas (diagnosis)", "malignant neoplasm of body of pancreas (diagnosis)", "Malignant neoplasm of other specified sites of pancreas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant pancreatic neoplasm", "shortest_name_length": 15}
{"curie": "MONDO:0004163", "names": ["bladder urachal urothelial carcinoma", "Bladder Urachal Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder urachal urothelial carcinoma", "shortest_name_length": 36}
{"curie": "MONDO:0003596", "names": ["spindle cell liposarcoma", "Spindle cell liposarcoma", "Spindle Cell Liposarcoma", "Atypical Spindle Cell Lipoma", "Spindle cell liposarcoma (disorder)", "Spindle cell liposarcoma (diagnosis)", "Fibrosarcoma-Like Lipomatous Neoplasm", "malignant neoplasm liposarcoma spindle cell", "Atypical Spindle Cell/Pleomorphic Lipomatous Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spindle cell liposarcoma", "shortest_name_length": 24}
{"curie": "MONDO:0006144", "names": ["cervical Wilms tumor", "Cervical Wilms Tumor", "cervical Wilms' tumor", "Cervical Nephroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical Wilms tumor", "shortest_name_length": 20}
{"curie": "UMLS:C0280365", "names": ["Relapsed Mouth Verrucous Carcinoma", "Recurrent Mouth Verrucous Carcinoma", "Relapsed Verrucous Carcinoma of Mouth", "Recurrent Verrucous Carcinoma of Mouth", "Recurrent Oral Cavity Verrucous Cancer", "Relapsed Oral Cavity Verrucous Carcinoma", "Relapsed Verrucous Carcinoma of the Mouth", "Recurrent Oral Cavity Verrucous Carcinoma", "oral cavity verrucous carcinoma, recurrent", "Recurrent Verrucous Carcinoma of the Mouth", "Relapsed Verrucous Carcinoma of Oral Cavity", "Recurrent Verrucous Carcinoma of Oral Cavity", "Relapsed Verrucous Carcinoma of the Oral Cavity", "Verrucous carcinoma of the oral cavity recurrent", "recurrent verrucous carcinoma of the oral cavity", "Recurrent Verrucous Carcinoma of the Oral Cavity", "verrucous carcinoma of the oral cavity, recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Verrucous carcinoma of the oral cavity recurrent", "shortest_name_length": 34}
{"curie": "UMLS:C0279739", "names": ["Lip Basal Cell Cancer", "Lip basal cell carcinoma", "basal carcinoma cell lip", "Lip Basal Cell Carcinoma", "lip basal cell carcinoma", "basal cell carcinoma, lip", "Basal Cell Carcinoma of Lip", "Basal Cell Carcinoma of the Lip"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lip basal cell carcinoma", "shortest_name_length": 21}
{"curie": "UMLS:C5419113", "names": ["Locally Advanced Synovial Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Synovial Sarcoma", "shortest_name_length": 33}
{"curie": "UMLS:C4763801", "names": ["Refractory B-Cell Prolymphocytic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory B-Cell Prolymphocytic Leukemia", "shortest_name_length": 41}
{"curie": "MONDO:0017725", "names": ["hexosaminidase A deficiency, juvenile form", "Tay-Sachs disease, b variant, juvenile form", "GM2 gangliosidosis, B variant, juvenile form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tay-Sachs disease, b variant, juvenile form", "shortest_name_length": 42}
{"curie": "UMLS:C4525662", "names": ["Stage II Ileal Neuroendocrine Tumor", "Stage II Ileal Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Ileal Neuroendocrine Tumor AJCC v8", "shortest_name_length": 35}
{"curie": "MONDO:0025708", "names": ["MMIHS2", "megacystis-microcolon-intestinal hypoperistalsis syndrome 2", "MEGACYSTIS-MICROCOLON-INTESTINAL HYPOPERISTALSIS SYNDROME 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "megacystis-microcolon-intestinal hypoperistalsis syndrome 2", "shortest_name_length": 6}
{"curie": "UMLS:C4683783", "names": ["RISS Stage I Plasma Cell Myeloma", "Revised International Staging System Stage I Plasma Cell Myeloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "RISS Stage I Plasma Cell Myeloma", "shortest_name_length": 32}
{"curie": "UMLS:C4725805", "names": ["Refractory Malignant Neoplasm of Multiple Primary Sites"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Malignant Neoplasm of Multiple Primary Sites", "shortest_name_length": 55}
{"curie": "UMLS:C1335054", "names": ["Non-Proliferating Breast Lesion", "Non-Proliferating Lesion of Breast", "Non-Proliferating Lesion of the Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Proliferating Breast Lesion", "shortest_name_length": 31}
{"curie": "UMLS:C0877377", "names": ["Skin tear", "Skin Tear", "skin tear", "tear skin", "Skin Tears", "skin tears", "Tear of skin", "Skin tear(s)", "skin tearing", "Traumatic tear of skin", "Traumatic tear of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin tear", "shortest_name_length": 9}
{"curie": "UMLS:C4727422", "names": ["Recurrent Ovarian Transitional Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Ovarian Transitional Cell Carcinoma", "shortest_name_length": 45}
{"curie": "MONDO:0005627", "names": ["HEAD NECK CANCER", "head neck cancer", "head cancer neck", "cancer head neck", "cancers head neck", "head/neck neoplasm", "of head neck cancer", "cancer of head neck", "Head and Neck Cancer", "head and neck cancer", "Head and neck cancer", "head and neck tumours", "head and neck neoplasm", "tumor of head and neck", "cancer of the neck head", "Cancer of Head and Neck", "Cancer of head and neck", "cancer of head and neck", "Head and neck cancer, NOS", "cancer of the head and neck", "Cancer of the Head and Neck", "craniocervical region cancer", "malignant head and neck tumor", "Malignant Head and Neck Tumor", "Malignant head and neck tumors", "cancer of craniocervical region", "Malignant Tumor of Head and Neck", "Malignant tumor of head and neck", "malignant head and neck neoplasm", "malignant tumor of head and neck", "Malignant Head and Neck Neoplasm", "head and neck malignant neoplasia", "Malignant tumour of head and neck", "HEAD AND NECK CANCER, UNKNOWN SITE", "Malignant Neoplasm of Head and Neck", "Malignant tumor of head and/or neck", "malignant neoplasm of head and neck", "malignant tumor of the head and neck", "Malignant Tumor of the Head and Neck", "Malignant tumour of head and/or neck", "malignant neoplasm of head and/or neck", "malignant neoplasm of the head and neck", "Malignant Neoplasm of the Head and Neck", "malignant craniocervical region neoplasm", "malignant neoplasm of craniocervical region", "Malignant tumor of head and/or neck (disorder)", "malignant neoplasm of head and/or neck (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "head and neck cancer", "shortest_name_length": 16}
{"curie": "MONDO:0016291", "names": ["Herrmann Opitz craniosynostosis", "craniosynostosis, Herrmann-Opitz type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniosynostosis, Herrmann-Opitz type", "shortest_name_length": 31}
{"curie": "UMLS:C4553675", "names": ["Stage IIIA Uterine Corpus Cancer AJCC v8", "Stage IIIA Uterine (including Endometrial) Cancer", "Stage IIIA Uterine Corpus Carcinoma or Carcinosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Uterine Corpus Cancer AJCC v8", "shortest_name_length": 40}
{"curie": "UMLS:C4744859", "names": ["Advanced Pancreatic Islet Cell Tumor", "Advanced Pancreatic Neuroendocrine Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Pancreatic Neuroendocrine Tumor", "shortest_name_length": 36}
{"curie": "MONDO:0004584", "names": ["cryptostromosis", "Cryptostromosis", "maple bark disease", "Maple-bark disease", "Maple bark strippers lung", "Maple-bark-stripper's lung", "maple-bark-stripper's lung", "Maple-bark-strippers' lung", "Maple-bark stripper's lung", "Maple-bark strippers' lung", "maple bark stripper's lung", "Maple bark strippers' lung", "maple-bark strippers' lung", "maple bark-strippers' lung", "maple bark strippers' lung", "Maple bark-strippers' lung", "MAPLE BARK STRIPPER DISEASE", "Maple-bark strippers' disease", "maple bark stripper's disease", "maple bark-strippers' disease", "Cryptostroma corticale; alveolitis", "alveolitis; Cryptostroma corticale", "Maple-bark strippers' lung (disorder)", "Alveolitis due to Cryptostroma corticale", "alveolitis due to cryptostroma corticale", "maple bark-strippers' disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maple bark strippers' lung", "shortest_name_length": 15}
{"curie": "UMLS:C0001890", "names": ["Akinetic Petit Mal", "Petit Mal, Akinetic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Akinetic Petit Mal", "shortest_name_length": 18}
{"curie": "MONDO:0025102", "names": ["Monkey Disease", "monkey disease", "Monkey Diseases", "Disease, Monkey", "disease, monkey", "monkey diseases", "diseases, monkey", "diseases monkeys", "Diseases, Monkey"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "monkey disease", "shortest_name_length": 14}
{"curie": "UMLS:C1334994", "names": ["Non-Neoplastic Axillary Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Axillary Disorder", "shortest_name_length": 32}
{"curie": "MONDO:0008397", "names": ["ALSG", "salivary gland; absent", "absence; salivary gland", "agenesis; salivary gland", "salivary gland; agenesis", "absence of salivary gland", "Absence of salivary gland", "salivary glands, absence of", "SALIVARY GLANDS, ABSENCE OF", "Salivary Glands, Absence of", "parotid aplasia or hypoplasia", "PAROTID APLASIA OR HYPOPLASIA", "Parotid Aplasia or Hypoplasia", "salivary glands, absence of, include", "Congenital absence of salivary gland", "absence of salivary gland (diagnosis)", "Absence of salivary gland, congenital", "Aplasia of lacrimal and salivary gland", "APLASIA OF LACRIMAL AND SALIVARY GLANDS", "Aplasia of Lacrimal and Salivary Glands", "aplasia of lacrimal and salivary glands", "Aplasia of lacrimal and salivary glands", "Congenital absence of salivary gland (disorder)", "Congenital absence of lacrimal puncta and salivary glands", "congenital absence of lacrimal puncta and salivary glands", "Congenital aplasia of lacrimal gland co-occurrent with congenital aplasia of salivary gland", "Congenital aplasia of lacrimal gland co-occurrent with congenital aplasia of salivary gland (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aplasia of lacrimal and salivary glands", "shortest_name_length": 4}
{"curie": "MONDO:0005288", "names": ["Bowel polyp", "intestine polyp", "polyp intestine", "Intestinal polyp", "intestinal polyp", "INTESTINAL POLYP", "Intestinal Polyp", "intestine polyps", "Intestinal polyps", "Polyp, Intestinal", "Intestinal Polyps", "intestinal polyps", "intestines polyps", "Polyp of intestine", "Polyps, Intestinal", "Polyp(s);intestine", "polyp of intestine", "intestinal polyp(s)", "intestinal polyp (disease)", "Polyp of intestine (disorder)", "polyp of intestine (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intestinal polyp", "shortest_name_length": 11}
{"curie": "UMLS:C4721792", "names": ["Ovarian Cancer Stage IIA", "Stage IIA Ovarian Cancer", "FIGO Stage IIA Ovarian Cancer", "AJCC Stage IIA Ovarian Cancer", "FIGO Stage IIA Cancer of Ovary", "Stage IIA Ovarian Cancer AJCC v7", "FIGO Stage IIA Ovarian Carcinoma", "Stage IIA Ovarian Cancer AJCC V6", "FIGO Stage IIA Carcinoma of Ovary", "FIGO Stage IIA Cancer of the Ovary", "Stage IIA Ovarian Epithelial Cancer", "FIGO Stage IIA Carcinoma of the Ovary", "Stage IIA Ovarian Cancer AJCC V6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Ovarian Cancer AJCC V6 and v7", "shortest_name_length": 24}
{"curie": "MONDO:0003251", "names": ["Granular Cell Esophagus Tumor", "esophagus granular cell tumor", "granular cell esophagus tumor", "Granular Cell Esophageal Tumor", "esophageal granular cell tumor", "Esophageal Granular Cell Tumor", "granular cell esophageal tumor", "granular cell esophagus neoplasm", "Granular Cell Tumor of Esophagus", "Granular cell tumor of esophagus", "granular cell tumor of esophagus", "Granular Cell Esophagus Neoplasm", "Esophageal Granular Cell Neoplasm", "esophageal granular cell neoplasm", "Granular cell tumour of oesophagus", "granular cell tumour of oesophagus", "granular cell neoplasm of esophagus", "granular cell esophagus myoblastoma", "Granular Cell Neoplasm of Esophagus", "Granular Cell Esophagus Myoblastoma", "Granular cell neoplasm of esophagus", "granular cell tumor of the esophagus", "esophageal granular cell myoblastoma", "Granular cell neoplasm of oesophagus", "Esophageal Granular Cell Myoblastoma", "Granular Cell Tumor of the Esophagus", "granular cell myoblastoma of esophagus", "Granular Cell Myoblastoma of Esophagus", "granular cell neoplasm of the esophagus", "Granular Cell Neoplasm of the Esophagus", "malignant granular cell esophageal tumor", "malignant granular cell esophageal tumour", "Granular Cell Myoblastoma of the Esophagus", "granular cell myoblastoma of the esophagus", "Granular cell neoplasm of esophagus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophageal granular cell tumor", "shortest_name_length": 29}
{"curie": "MONDO:0019995", "names": ["PRTH", "Peripheral Resistance to Thyroid Hormone", "Peripheral resistance to thyroid hormone", "peripheral resistance to thyroid hormones", "Peripheral resistance to thyroid hormone (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peripheral resistance to thyroid hormones", "shortest_name_length": 4}
{"curie": "MONDO:0021635", "names": ["neurocristopathy", "disorder of neural crest development", "neural crest cell development disease", "disorder of neural crest cell development"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurocristopathy", "shortest_name_length": 16}
{"curie": "MONDO:0016570", "names": ["PULMONARY LYMPHOMA", "Pulmonary lymphoma", "pulmonary lymphoma", "lymphoma involving lung", "lymphoma primary pulmonary", "Primary pulmonary lymphoma", "primary pulmonary lymphoma", "lymphoma involving the lung", "lymphoma involving lung (diagnosis)", "Primary pulmonary lymphoma (disorder)", "Primary pulmonary lymphoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary pulmonary lymphoma", "shortest_name_length": 18}
{"curie": "MONDO:0019368", "names": ["Focal COD", "Florid COD", "Gigantiform cementoma", "Gigantiform Cementoma", "Focal Osseous Dysplasia", "Florid osseous dysplasia", "florid osseous dysplasia", "Florid Osseous Dysplasia", "Familial multiple cementoma", "Focal cemento-osseous dysplasia", "focal cemento-osseous dysplasia", "Focal Cemento-Osseous Dysplasia", "Florid Cemento-Osseous Dysplasia", "Florid cemento-osseous dysplasia", "florid cemento-osseous dysplasia", "Florid cemento-osseous dysplasia (disorder)", "Focal cemento-osseous dysplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "florid cemento-osseous dysplasia", "shortest_name_length": 9}
{"curie": "UMLS:C4553160", "names": ["Recurrent Anaplastic Oligoastrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Anaplastic Oligoastrocytoma", "shortest_name_length": 37}
{"curie": "MONDO:0012251", "names": ["EKV3", "MEDNIK", "MEDNIK syndrome", "MEDNIK SYNDROME", "Erythrokeratodermia Variabilis 3", "ERYTHROKERATODERMIA VARIABILIS 3", "erythrokeratodermia variabilis 3", "Erythrokeratodermia variabilis 3", "ERYTHROKERATODERMIA VARIABILIS 3 (disorder)", "Erythrokeratodermia variabilis Kamouraska type", "Erythrokeratodermia Variabilis, Kamouraska Type", "erythrokeratodermia variabilis, Kamouraska type", "ERYTHROKERATODERMIA VARIABILIS, KAMOURASKA TYPE", "mental retardation, enteropathy, deafness, neuropathy, ichthyosis, keratodermia", "intellectual disability, enteropathy, deafness, neuropathy, ichthyosis, keratodermia", "mental retardation, enteropathy, deafness, peripheral neuropathy, ichthyosis, and keratoderma", "MENTAL RETARDATION, ENTEROPATHY, DEAFNESS, PERIPHERAL NEUROPATHY, ICHTHYOSIS, AND KERATODERMA", "intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, and keratoderma", "Intellectual disability-enteropathy-deafness-peripheral neuropathy-ichthyosis-keratodermia syndrome", "intellectual disability-enteropathy-deafness-peripheral neuropathy-ichthyosis-keratodermia syndrome", "Intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratoderma syndrome", "intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratoderma syndrome", "Intellectual disability-enteropathy-hearing loss-peripheral neuropathy-ichthyosis-keratodermia syndrome", "MEDNIK (mental retardation, enteropathy, deafness, peripheral neuropathy, ichtyosis, keratodermia) syndrome", "IMPAIRED INTELLECTUAL DEVELOPMENT, ENTEROPATHY, DEAFNESS, PERIPHERAL NEUROPATHY, ICHTHYOSIS, AND KERATODERMA", "Intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratoderma syndrome (disorder)", "intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratoderma syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MEDNIK syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0270729", "names": ["drugs; parkinsonism", "PARKINSON DRUG INDUCED", "drug induced parkinsons", "Parkinsonism due to drug", "parkinsonism due to drug", "Drug-induced parkinsonism", "drug induced parkinsonism", "Parkinsonism due to drugs", "PARKINSONISM DRUG INDUCED", "PARKINSONISM, DRUG-INDUCED", "parkinsonism; due to drugs", "Parkinsonism caused by drug", "Parkinsonism caused by drug (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parkinsonism due to drug", "shortest_name_length": 19}
{"curie": "UMLS:C5419187", "names": ["Refractory Cutaneous Squamous Cell Carcinoma of the Head and Neck"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Cutaneous Squamous Cell Carcinoma of the Head and Neck", "shortest_name_length": 65}
{"curie": "MONDO:0018685", "names": ["Incessant infant ventricular tachycardia", "incessant infant ventricular tachycardia", "Incessant infant ventricular tachycardia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "incessant infant ventricular tachycardia", "shortest_name_length": 40}
{"curie": "MONDO:0001092", "names": ["colon leiomyoma", "Colon Leiomyoma", "Colonic leiomyoma", "colonic leiomyoma", "Colonic Leiomyoma", "Leiomyoma of Colon", "leiomyoma of colon", "leiomyoma of the colon", "Leiomyoma of the Colon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colon leiomyoma", "shortest_name_length": 15}
{"curie": "MONDO:0700137", "names": ["bovine lymphosarcoma", "Bovine Lymphosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bovine lymphosarcoma", "shortest_name_length": 20}
{"curie": "MONDO:0016087", "names": ["Copenhagen syndrome", "Progressive non-infectious anterior vertebral fusion", "progressive non-infectious anterior vertebral fusion", "Progressive non-infectious anterior vertebral fusion (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive non-infectious anterior vertebral fusion", "shortest_name_length": 19}
{"curie": "UMLS:C0269672", "names": ["Maternal obesity syndrome", "WEIGHT GAIN PREGNANCY EXCESSIVE", "pregnancy; excessive weight gain", "Excessive weight gain in pregnancy", "Excessive Weight Gain in Pregnancy", "excessive weight gain in pregnancy", "Maternal obesity without hypertension", "excessive weight gain in pregnancy (diagnosis)", "Excessive weight gain in pregnancy, unspecified trimester"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Excessive weight gain in pregnancy", "shortest_name_length": 25}
{"curie": "UMLS:C4726598", "names": ["Abdominal Rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abdominal Rhabdomyosarcoma", "shortest_name_length": 26}
{"curie": "UMLS:C5420232", "names": ["Head and Neck Langerhans Cell Histiocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Head and Neck Langerhans Cell Histiocytosis", "shortest_name_length": 43}
{"curie": "MONDO:8000014", "names": ["Hughes syndrome", "Lupus anticoagulant, familial", "LUPUS ANTICOAGULANT, FAMILIAL", "Familial antiphospholipid syndrome", "familial antiphospholipid syndrome", "ANTIPHOSPHOLIPID SYNDROME, FAMILIAL", "antiphospholipid syndrome, familial", "Antiphospholipid Syndrome, Familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial antiphospholipid syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0004846", "names": ["ABLATIO PLACENTAE", "PLACENTA ABRUPTIO", "Abruptio placenta", "ablatio placentae", "ABRUPTIO PLACENTA", "Placenta abruptio", "Abruptio Placenta", "Ablatio placentae", "threaten abortion", "placenta abruptio", "abruptio placenta", "Abruptio placentae", "placenta; abruptio", "placenta abruption", "abruptio placentae", "ABRUPTIO PLACENTAE", "Abruptio Placentae", "placentae abruptio", "placentae; ablatio", "Couvelaire placenta", "ABORTION THREATENED", "Couvelaire syndrome", "threatened abortion", "Threatened abortion", "Placental Abruption", "Abortion threatened", "Threatened Abortion", "abruption placental", "Placental abruption", "Abortion;threatened", "placental abruption", "abortion threatened", "Abortion, threatened", "threatened; abortion", "ABORTION, THREATENED", "Abruption, Placental", "placenta; detachment", "Abortion, Threatened", "abortion; threatened", "Placental Abruptions", "Threatened Abortions", "placental separation", "Placental separation", "accidental hemorrhage", "Abruptions, Placental", "Accidental hemorrhage", "Detachment of placenta", "Accidental haemorrhage", "accidental haemorrhage", "Miscarriage;threatened", "Abruptio placentae NOS", "Threatened miscarriage", "threatened miscarriage", "Threatened Miscarriage", "Miscarriage, Threatened", "miscarriage; threatened", "Threatened Miscarriages", "miscarriage threatening", "threatened; miscarriage", "Threatened abortion, NOS", "Abruptio placentae syndrome", "placental abruption (disease)", "Prematurely separated placenta", "PLACENTA, PREMATURE SEPARATION", "Threatened abortion (disorder)", "Placental abruption (disorder)", "premature; separation placenta", "Premature placental detachment", "pregnancy; threatened abortion", "placenta abruption (diagnosis)", "Premature placental separation", "Threatened abortion, antepartum", "pregnancy; abortion, threatened", "Premature separation of placenta", "premature separation of placenta", "Threatened abortion (antepartum)", "Premature Separation of Placenta", "Premature detachment of placenta", "Accidental antepartum hemorrhage", "antepartum hemorrhage accidental", "Accidental antepartum haemorrhage", "pregnancy with threatened abortion", "pregnancy; placenta, separation, premature", "pregnancy; separation, placental, premature", "Accidental antepartum hemorrhage (diagnosis)", "Premature separation of placenta, unspecified", "pregnancy with threatened abortion (diagnosis)", "Premature detachment of normally implanted placenta", "Premature separation of normally implanted placenta", "Abruptio Placentae, Premature Separation of Placenta", "Abruptio placentae, premature separation of placenta", "Premature separation of placenta [abruptio placentae]", "Threatened abortion, antepartum condition or complication", "Premature separation of placenta, unspecified as to episode of care", "Premature separation of placenta, unspecified, unspecified trimester", "Premature separation of placenta, unspecified as to episode of care or not applicable"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "placental abruption", "shortest_name_length": 17}
{"curie": "UMLS:C3887518", "names": ["Myxopapillary Ependymoma", "Adult Myxopapillary Ependymoma", "adult myxopapillary ependymoma", "myxopapillary ependymoma, adult", "adult well-differentiated ependymoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Myxopapillary Ependymoma", "shortest_name_length": 24}
{"curie": "MONDO:0018095", "names": ["Weaver-Williams syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Weaver-Williams syndrome", "shortest_name_length": 24}
{"curie": "UMLS:C2939462", "names": ["Primary amyloidosis", "Systemic light chain disease", "Immunoglobulin Deposition Disease", "Immunoglobulin deposition disease", "Monoclonal Immunoglobulin Deposition Disease", "monoclonal immunoglobulin deposition disease", "Immunoglobulin deposition disease (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immunoglobulin deposition disease", "shortest_name_length": 19}
{"curie": "MONDO:0002556", "names": ["macrocystic neurilemmoma", "Microcystic/Reticular Schwannoma", "microcystic/reticular schwannoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcystic/reticular schwannoma", "shortest_name_length": 24}
{"curie": "UMLS:C0860434", "names": ["fluid electrolyte imbalance", "electrolyte fluid imbalance", "electrolytes fluid imbalance", "electrolyte fluid imbalances", "fluid and electrolyte imbalance", "Fluid and electrolyte imbalance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fluid and electrolyte imbalance", "shortest_name_length": 27}
{"curie": "UMLS:C4763503", "names": ["Adrenal Gland Ganglioneuroblastoma, Intermixed"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adrenal Gland Ganglioneuroblastoma, Intermixed", "shortest_name_length": 46}
{"curie": "MONDO:0010377", "names": ["MYP13", "myopia 13", "Myopia 13", "MYOPIA 13", "myopia 13, X-linked", "MYOPIA 13, X-LINKED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopia 13, X-linked", "shortest_name_length": 5}
{"curie": "UMLS:C5418917", "names": ["Unresectable Primary Peritoneal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Primary Peritoneal Adenocarcinoma", "shortest_name_length": 46}
{"curie": "MONDO:0007035", "names": ["Keratosis nigricans", "keratosis nigricans", "Acanthosis Nigrican", "KERATOSIS NIGRICANS", "keratosis; nigricans", "nigricans; keratosis", "Acanthosis Nigricans", "ACANTHOSIS NIGRICANS", "Nigrican, Acanthosis", "Acanthosis nigricans", "acanthosis nigricans", "Nigricans, Acanthosis", "an - acanthosis nigricans", "AN - Acanthosis nigricans", "Darkened and thickened skin", "Acquired acanthosis nigricans", "acanthosis nigricans (disease)", "Acanthosis nigricans (disorder)", "acanthosis nigricans (diagnosis)", "Acquired acanthosis nigricans (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acanthosis nigricans", "shortest_name_length": 19}
{"curie": "UMLS:C0472387", "names": ["cerebral edema vasogenic", "Vasogenic Cerebral Edema", "vasogenic cerebral edema", "cerebral vasogenic edema", "Vasogenic cerebral edema", "Vasogenic cerebral oedema", "Edema, Vasogenic Cerebral", "Cerebral Edema, Vasogenic", "Cerebral Edemas, Vasogenic", "Vasogenic cerebral edema (disorder)", "cerebral edema vasogenic (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vasogenic Cerebral Edema", "shortest_name_length": 24}
{"curie": "MONDO:0013965", "names": ["LCCS4", "LETHAL CONGENITAL CONTRACTURE SYNDROME 4", "lethal congenital contracture syndrome 4", "MYBPC1 lethal congenital contracture syndrome", "lethal congenital contracture syndrome type 4", "lethal congenital contracture syndrome caused by mutation in MYBPC1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal congenital contracture syndrome 4", "shortest_name_length": 5}
{"curie": "MONDO:0000295", "names": ["acanthocephaliasis", "Acanthocephaliasis", "Acanthocephalan infection", "infection by Acanthocephala", "infection by acanthocephala", "Infection by Acanthocephala", "Disease due to Acanthocephala", "disease due to Acanthocephala", "DISEASES DUE TO ACANTHOCEPHALA", "infection by thorny-headed worm", "Infection by thorny-headed worm", "disease caused by Acanthocephala", "Disease caused by Acanthocephala", "Infection by Acanthocephala, NOS", "Acanthocephala infectious disease", "Acanthocephala disease or disorder", "infection by acanthocephala (diagnosis)", "Acanthocephala caused disease or disorder", "Disease caused by Acanthocephala (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acanthocephaliasis", "shortest_name_length": 18}
{"curie": "UMLS:C2985224", "names": ["Substance Intoxication Delirium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Substance Intoxication Delirium", "shortest_name_length": 31}
{"curie": "UMLS:C0155679", "names": ["acute pericarditis", "Pericarditis;acute", "Acute Pericarditis", "Acute pericarditis", "pericarditis acute", "PERICARDITIS ACUTE", "acute; pericarditis", "PERICARDITIS, ACUTE", "pericarditis; acute", "Acute pericarditis NOS", "Acute pericarditis, NOS", "Acute pericarditis (disorder)", "acute pericarditis (diagnosis)", "Acute pericarditis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute pericarditis", "shortest_name_length": 18}
{"curie": "MONDO:0005861", "names": ["MDR-TB", "MDR TB", "MDR Tuberculosis", "mdr tuberculosis", "Tuberculosis, MDR", "multidrug-resistant TB", "Multidrug-Resistant TB", "multidrug-resistant tuberculosis", "Multidrug resistant tuberculosis", "multidrug resistant tuberculosis", "Multidrug-resistant tuberculosis", "Multidrug-Resistant Tuberculosis", "Multi-Drug Resistant Tuberculosis", "multi drug resistant tuberculosis", "Tuberculosis, Multidrug Resistant", "Tuberculosis, Multidrug-Resistant", "multi-drug-resistant tuberculosis", "TUBERCULOSIS MULTI DRUG RESISTANT", "multi-drug resistant tuberculosis", "Tuberculosis, Multi Drug Resistant", "Tuberculosis, Multi-Drug Resistant", "Multidrug resistant tuberculosis (disorder)", "multi-drug-resistant tuberculosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multidrug-resistant tuberculosis", "shortest_name_length": 6}
{"curie": "UMLS:C4683588", "names": ["Lugano Classification Stage II Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage II Hodgkin Lymphoma AJCC v8", "shortest_name_length": 55}
{"curie": "UMLS:C1562435", "names": ["PSN-P", "Placental site nodule", "Placental Site Nodule", "Placental Site Nodule or Plaque", "Placental site nodule (disorder)", "Placental Site Nodule and Plaque", "Placental site nodule (diagnosis)", "Placental site nodule (morphologic abnormality)", "pregnancy complications: gestational trophoblastic lesion placental site nodule"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Placental site nodule", "shortest_name_length": 5}
{"curie": "UMLS:C0278716", "names": ["recurrent Wilms tumor", "Wilms tumor, recurrent", "recurrent Wilm's tumor", "Wilms' tumor, recurrent", "Wilm's tumor, recurrent", "recurrent nephroblastoma", "nephroblastoma, recurrent", "Relapsed Renal Adenosarcoma", "Recurrent Renal Wilms Tumor", "Relapsed Renal Wilms' Tumor", "Recurrent Kidney Wilms Tumor", "Relapsed Kidney Adenosarcoma", "Recurrent Renal Adenosarcoma", "Recurrent Renal Wilms' Tumor", "Recurrent Kidney Adenosarcoma", "Relapsed Kidney Nephroblastoma", "Recurrent Kidney Nephroblastoma", "recurrent Wilms tumor and other childhood kidney tumors", "recurrent Wilms' tumor and other childhood kidney tumors"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Kidney Wilms Tumor", "shortest_name_length": 21}
{"curie": "MONDO:0032884", "names": ["EDFAOB", "ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies", "ECTODERMAL DYSPLASIA WITH FACIAL DYSMORPHISM AND ACRAL, OCULAR, AND BRAIN ANOMALIES", "ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies", "shortest_name_length": 6}
{"curie": "UMLS:C0751585", "names": ["West Nile Fever Meningoencephalitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "West Nile Fever Meningoencephalitis", "shortest_name_length": 35}
{"curie": "MONDO:0009493", "names": ["RRNS", "richards rundle syndrome", "richards-rundle syndrome", "RICHARDS-RUNDLE SYNDROME", "RICHARDS-RUNDLE syndrome", "Richards-Rundle syndrome", "richard rundles syndrome", "Richards-Rundle syndrome (RRS)", "Richards-Rundle syndrome (disorder)", "familial ataxia-hypogonadism syndrome", "Familial ataxia-hypogonadism syndrome", "ketoaciduria-mental deficiency syndrome", "Ketoaciduria-mental deficiency syndrome", "ataxia-deafness-mental retardation syndrome", "ATAXIA-DEAFNESS-MENTAL RETARDATION SYNDROME", "ataxia-deafness-intellectual disability syndrome", "ataxia-deafness-retardation syndrome with ketoaciduria", "Ketoaciduria With Mental Deficiency And Other Features", "Ataxia-deafness-retardation syndrome with ketoaciduria", "ketoaciduria - intellectual disability - ataxia - deafness", "ketoaciduria-intellectual disability-ataxia-deafness syndrome", "Ketoaciduria-intellectual disability-ataxia-deafness syndrome", "Ketoaciduria-intellectual disability-ataxia-hearing loss syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Richards-Rundle syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C2363949", "names": ["Injection site exfoliation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site exfoliation", "shortest_name_length": 26}
{"curie": "UMLS:C0878649", "names": ["Gastric Metaplastic Polyp", "Gastric Hyperplastic Polyp", "Gastric hyperplastic polyp", "hyperplastic gastric polyp", "gastric hyperplastic polyps", "Gastric polyp, hyperplastic", "benign gastric hyperplastic polyps", "benign gastric hyperplastic polyps (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric hyperplastic polyp", "shortest_name_length": 25}
{"curie": "UMLS:C0333650", "names": ["FAT ATROPHY", "Fat Atrophy", "fat atrophy", "Fat atrophy", "Fatty atrophy", "atrophy; fatty", "fatty; atrophy", "Atrophy, fatty", "Fat atrophy NOS", "Adipositas ex vacuo", "Adipose Tissue Atrophy", "fat atrophy (diagnosis)", "Fatty atrophy (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adipose Tissue Atrophy", "shortest_name_length": 11}
{"curie": "UMLS:C1274191", "names": ["Lyell syndrome caused by drug", "Toxic epidermal necrolysis due to drug", "Toxic epidermal necrolysis caused by drug", "Toxic epidermal necrolysis caused by drug (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Toxic epidermal necrolysis due to drug", "shortest_name_length": 29}
{"curie": "MONDO:0009609", "names": ["HMAG", "cblG", "methionine synthase deficiency", "METHIONINE SYNTHASE DEFICIENCY", "methylcobalamin deficiency type cblG", "Methylcobalamin deficiency type cblG", "CBL G type Methylcobalamin deficiency", "methylcobalamin deficiency Cbl G type", "methylcobalamin deficiency, cblG type", "METHYLCOBALAMIN DEFICIENCY, cblG TYPE", "Methylcobalamin Deficiency, CblG Type", "Methylcobalamin deficiency type cbl G", "homocystinuria-megaloblastic anemia cblG type", "Methylcobalamin deficiency type cbl G (disorder)", "homocystinuria due to defect in methylation Cbl g", "Functional methionine synthase deficiency type cblG", "functional methionine synthase deficiency type cblG", "methylmalonic aciduria and homocystinuria type cblG", "homocystinuria-megaloblastic anemia, cblG complementation type", "HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, cblG COMPLEMENTATION TYPE", "homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism cblG complementation type", "homocystinuria-megaloblastic Anemia due to defect in cobalamin metabolism, cblG complementation type", "HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA DUE TO DEFECT IN COBALAMIN METABOLISM, cblG COMPLEMENTATION TYPE", "Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblG Complementation Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "methylcobalamin deficiency type cblG", "shortest_name_length": 4}
{"curie": "UMLS:C0040938", "names": ["trichophytosis", "Trichophytosis", "Trichophytoses", "Trichophytosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Trichophytosis", "shortest_name_length": 14}
{"curie": "MONDO:0015729", "names": ["Trisomy 16", "mosaic trisomy 16", "Mosaic trisomy 16", "Trisomy 16 mosaicism", "trisomy 16 mosaicism", "Chromosome 16, trisomy", "Mosaic trisomy type 16", "Mosaic trisomy 16 syndrome", "Mosaic trisomy chromosome 16", "Mosaic trisomy 16 syndrome (disorder)", "Mosaic trisomy 16 syndrome (diagnosis)", "anomaly of chromosome pair mosaic trisomy 16 syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mosaic trisomy 16", "shortest_name_length": 10}
{"curie": "MONDO:0012579", "names": ["PAP", "aPAP", "APAP", "iPAP", "PAP acquired", "Pap, acquired", "PAP, ACQUIRED", "idiopathic PAP", "Autoimmune PAP", "autoimmune PAP", "acquired pulmonary alveolar proteinosis", "pulmonary alveolar proteinosis acquired", "Pulmonary Alveolar Proteinosis, Acquired", "PULMONARY ALVEOLAR PROTEINOSIS, ACQUIRED", "pulmonary alveolar proteinosis, acquired", "pulmonary alveolar proteinosis autoimmune", "idiopathic pulmonary alveolar proteinosis", "autoimmune pulmonary alveolar proteinosis", "Autoimmune pulmonary alveolar proteinosis", "PULMONARY ALVEOLAR PROTEINOSIS, AUTOIMMUNE", "pulmonary alveolar proteinosis, autoimmune", "Pulmonary Alveolar Proteinosis, Autoimmune", "pulmonary alveolar lipoproteinosis acquired", "PULMONARY ALVEOLAR LIPOPROTEINOSIS, ACQUIRED", "Pulmonary Alveolar Lipoproteinosis, Acquired", "pulmonary alveolar lipoproteinosis, acquired", "Autoimmune pulmonary alveolar proteinosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune pulmonary alveolar proteinosis", "shortest_name_length": 3}
{"curie": "UMLS:C0267356", "names": ["Duodenal perforation", "duodenal perforation", "Perforation duodenal", "Duodenal Perforation", "duodenal perforations", "Perforation of duodenum", "Duodenal perforation (disorder)", "duodenal perforation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Duodenal perforation", "shortest_name_length": 20}
{"curie": "MONDO:0010433", "names": ["SLEB15", "systemic lupus erythematosus, susceptibility to, 15", "SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 15"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "systemic lupus erythematosus, susceptibility to, 15", "shortest_name_length": 6}
{"curie": "UMLS:C0277585", "names": ["Drug Intolerance", "drug intolerance", "Drug intolerance", "DRUG INTOLERANCE", "drugs intolerance", "Intolerance to drug", "Drug intolerance NOS", "Drug intolerance, NOS", "Intolerance to drug (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intolerance to drug", "shortest_name_length": 16}
{"curie": "MONDO:0017727", "names": ["fixed subaortic stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fixed subaortic stenosis", "shortest_name_length": 24}
{"curie": "MONDO:0013950", "names": ["PBD11B", "peroxisome biogenesis disorder 11B", "PEROXISOME BIOGENESIS DISORDER 11B", "peroxisome biogenesis disorder type 11B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder 11B", "shortest_name_length": 6}
{"curie": "MONDO:0100273", "names": ["GNPAT deficiency", "glyceronephosphate O-acyltransferase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glyceronephosphate O-acyltransferase deficiency", "shortest_name_length": 16}
{"curie": "UMLS:C0280359", "names": ["Stage IV Lip Basal Cell Cancer", "Stage IV Lip Basal Cell Carcinoma", "lip basal cell carcinoma, stage IV", "lip basal cell carcinoma, metastatic", "Stage IV Basal Cell Carcinoma of Lip", "Stage IV Basal Cell Carcinoma of the Lip", "stage IV basal cell carcinoma of the lip", "basal cell carcinoma of the lip, stage IV", "metastatic basal cell carcinoma of the lip", "basal cell carcinoma of the lip, metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Lip Basal Cell Carcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0009319", "names": ["PKAN", "NBIA1", "NBIA 1", "Hallervorden-Spatz", "Hallervorden Spatz Disease", "hallervorden spatz disease", "HALLERVORDEN-SPATZ DISEASE", "Hallervorden-Spatz Disease", "Hallervorden-Spatz disease", "hallervorden-spatz disease", "Hallervorden Spatz Syndrome", "Hallervorden-Spatz syndrome", "Hallervorden-Spatz Syndrome", "hallervorden-spatz syndrome", "Pigmentary Pallidal Atrophy", "Pigmentary pallidal atrophy", "hallervorden spatz syndrome", "Pallidal Atrophy, Pigmentary", "pigmentary pallidal degeneration", "Pigmentary pallidal degeneration", "Pigmentary Pallidal Degeneration", "Degeneration, Pigmentary Pallidal", "degeneration; pallidal pigmentary", "pallidal pigmentary; degeneration", "pigmentary; degeneration, pallidal", "Juvenile-Onset Neuroaxonal Dystrophy", "neuroaxonal dystrophy, late infantile", "Dystrophy, Juvenile-Onset Neuroaxonal", "Neuroaxonal Dystrophy, Juvenile Onset", "Neuroaxonal Dystrophy, Juvenile-Onset", "Juvenile-Onset Neuroaxonal Dystrophies", "Dystrophies, Juvenile-Onset Neuroaxonal", "Neuroaxonal Dystrophies, Juvenile-Onset", "brain Iron Accumulation type I syndrome", "Brain Iron Accumulation Type I Syndrome", "brain iron accumulation type I syndrome", "PKAN NEUROAXONAL DYSTROPHY, JUVENILE-ONSET", "PKAN Neuroaxonal Dystrophy, Juvenile-Onset", "PKAN Neuroaxonal Dystrophy, Juvenile Onset", "Pkan neuroaxonal dystrophy, juvenile-onset", "Pigmentary pallidal degeneration (disorder)", "Pantothenate kinase-associated neurodegeneration", "pantothenate kinase-associated neurodegeneration", "Neurodegeneration With Brain Iron Accumulation 1", "pigmentary; degeneration, pallidal (progressive)", "Pantothenate Kinase-Associated Neurodegeneration", "PANTOTHENATE KINASE-ASSOCIATED NEURODEGENERATION", "degeneration; pigmentary, pallidal (progressive)", "neurodegeneration with brain iron accumulation 1", "Pantothenate Kinase Associated Neurodegeneration", "NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1", "Neurodegeneration, Pantothenate Kinase-Associated", "Neurodegeneration with Brain Iron Accumulation Type 1", "neurodegeneration with brain iron accumulation type 1", "Neurodegeneration with brain iron accumulation type 1", "Pantothenate kinase-associated neurodegeneration (PKAN)", "Pantothenate kinase-associated neurodegeneration (PKAN) (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pantothenate kinase-associated neurodegeneration", "shortest_name_length": 4}
{"curie": "MONDO:0007556", "names": ["EBSMP", "EBS2F", "EBS-MP", "EBS with mottled pigmentation", "Epidermolysis bullosa simplex-MP", "Simple epidermolysis bullosa with mottled pigmentation", "Epidermolysis bullosa simplex with mottled pigmentation", "epidermolysis bullosa simplex with mottled pigmentation", "EPIDERMOLYSIS BULLOSA SIMPLEX WITH MOTTLED PIGMENTATION", "epidermolysis bullosa simplex 2F, with mottled pigmentation", "EPIDERMOLYSIS BULLOSA SIMPLEX 2F, WITH MOTTLED PIGMENTATION", "Epidermolysis bullosa simplex with mottled pigmentation (disorder)", "Speckled hyperpigmentation, palmo-plantar punctate keratoses and childhood blistering", "speckled hyperpigmentation, palmo-plantar punctate keratoses and childhood blistering", "speckled hyperpigmentation with punctate palmoplantar keratoses and childhood blistering", "SPECKLED HYPERPIGMENTATION WITH PUNCTATE PALMOPLANTAR KERATOSES AND CHILDHOOD BLISTERING", "Speckled Hyperpigmentation With Punctate Palmoplantar Keratoses And Childhood Blistering"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolysis bullosa simplex 2F, with mottled pigmentation", "shortest_name_length": 5}
{"curie": "MONDO:0010116", "names": ["Thoracomelic Dysplasia", "Thoracomelic dysplasia", "thoraco-limb dysplasia", "Thoraco-Limb Dysplasia", "THORACOMELIC DYSPLASIA", "thoracomelic dysplasia", "'THORACO-LIMB' DYSPLASIA", "'thoraco-limb' dysplasia", "Rivera-Perez-Salas syndrome", "Rivera Perez Salas syndrome", "Thoracolimb dysplasia Rivera type", "Thoracomelic dysplasia (disorder)", "thoracolimb dysplasia, Rivera type", "Thoracolimb dysplasia, Rivera type", "Thoraco limb dysplasia Rivera type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thoracomelic dysplasia", "shortest_name_length": 22}
{"curie": "MONDO:0012821", "names": ["CRCS5", "colorectal cancer, susceptibility to, 5", "COLORECTAL CANCER, SUSCEPTIBILITY TO, 5", "COLORECTAL CANCER, SUSCEPTIBILITY TO, ON CHROMOSOME 10", "colorectal cancer, susceptibility to, on chromosome 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorectal cancer, susceptibility to, 5", "shortest_name_length": 5}
{"curie": "MONDO:0015697", "names": ["Immunoglobulin Heavy Chain Deletion", "Immunoglobulin heavy chain deletion", "Immunoglobulin heavy chain deficiency", "immunoglobulin heavy chain deficiency", "Immunoglobulin heavy chain deficiency (disorder)", "Immunoglobulin heavy chain deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunoglobulin heavy chain deficiency", "shortest_name_length": 35}
{"curie": "UMLS:C0677711", "names": ["Stage II Lymphoblastic Lymphoma", "NonContiguous Adult Lymphoblastic Lymphoma Stage II", "noncontiguous adult lymphoblastic lymphoma stage II", "noncontiguous stage II adult lymphoblastic lymphoma", "Non-Contiguous Stage II Adult Lymphoblastic Lymphoma", "adult non-contiguous stage II lymphoblastic lymphoma", "Stage II Adult Non-Contiguous Lymphoblastic Lymphoma", "Stage II Non-Contiguous Adult Lymphoblastic Lymphoma", "Non-Contiguous Adult Lymphoblastic Lymphoma Stage II", "stage II adult non-contiguous lymphoblastic lymphoma", "adult non-contiguous lymphoblastic lymphoma stage II", "Adult Non-Contiguous Lymphoblastic Lymphoma Stage II", "Adult Non-Contiguous Stage II Lymphoblastic Lymphoma", "stage II non-contiguous adult lymphoblastic lymphoma", "non-contiguous stage II adult lymphoblastic lymphoma", "non-contiguous adult lymphoblastic lymphoma stage II", "Ann Arbor Stage II Non-Contiguous Adult Lymphoblastic Lymphoma", "stage II non-contiguous adult precursor lymphoblastic lymphoma", "Stage II Non-Contiguous Adult Precursor Lymphoblastic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage II Non-Contiguous Adult Lymphoblastic Lymphoma", "shortest_name_length": 31}
{"curie": "MONDO:0060624", "names": ["NDAGSCW", "NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER", "neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter", "neurodevelopmental disorder with ataxic GAIT, absent speech, and decreased cortical WHITE matter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter", "shortest_name_length": 7}
{"curie": "MONDO:0035639", "names": ["MPAL with t(9;22)(q34.1;q11.2); BCR-ABL1", "mixed phenotype acute leukemia with t(9;22)(q34.1;q11.2)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed phenotype acute leukemia with t(9;22)(q34.1;q11.2)", "shortest_name_length": 40}
{"curie": "UMLS:C3665601", "names": ["Epileptic encephalopathy, Lennox-Gastaut type", "Childhood Epileptic Encephalopathy with Diffuse Slow Spikes and Waves"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epileptic encephalopathy, Lennox-Gastaut type", "shortest_name_length": 45}
{"curie": "MONDO:0005621", "names": ["Brain Vascular trauma", "vascular brain injury", "Brain Vascular Trauma", "Brain Vascular Injury", "Vascular Brain injury", "Vascular Brain Injury", "Brain Vascular injury", "Vascular Trauma, Brain", "Vascular trauma, Brain", "Brain injury, Vascular", "Brain Injury, Vascular", "Injury, Brain Vascular", "injury, Brain Vascular", "trauma, Brain Vascular", "Cerebrovascular Trauma", "injury, Vascular Brain", "Vascular injury, Brain", "Vascular Injury, Brain", "Vascular Traumas, Brain", "Vascular Brain Injuries", "trauma, cerebrovascular", "Trauma, Cerebrovascular", "injury, Vascular, Brain", "Injury, Vascular, Brain", "injury; cerebral vessels", "Injuries, Brain Vascular", "Brain Injuries, Vascular", "cerebral vessels; injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vascular brain injury", "shortest_name_length": 21}
{"curie": "UMLS:C0855020", "names": ["Lentigo maligna recurrent", "Lentigo Maligna Recurrent", "Recurrent Lentigo Maligna Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lentigo maligna recurrent", "shortest_name_length": 25}
{"curie": "MONDO:0003614", "names": ["intravenous leiomyomatosis", "Intravenous Leiomyomatosis", "Intravenous leiomyomatosis", "Intravenous Leiomyomatosis of Uterus", "Intravenous leiomyomatosis (disorder)", "Intravascular Leiomyomatosis of Uterus", "intravenous leiomyomatosis (diagnosis)", "Intravenous Leiomyomatosis of the Uterus", "Uterine Corpus Intravenous Leiomyomatosis", "Intravascular Leiomyomatosis of the Uterus", "Intravenous leiomyomatosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intravenous leiomyomatosis", "shortest_name_length": 26}
{"curie": "MONDO:0030987", "names": ["VCTERL", "VCTERL syndrome", "VCTERL SYNDROME", "VERTEBRAL, CARDIAC, TRACHEOESOPHAGEAL, RENAL, AND LIMB DEFECTS", "vertebral, cardiac, tracheoesophageal, renal, and limb defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vertebral, cardiac, tracheoesophageal, renal, and limb defects", "shortest_name_length": 6}
{"curie": "MONDO:0017461", "names": ["Familial isolated clinodactyly of finger", "Familial isolated clinodactyly of fingers", "familial isolated clinodactyly of fingers", "Familial isolated clinodactyly of finger (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial isolated clinodactyly of fingers", "shortest_name_length": 40}
{"curie": "MONDO:0011172", "names": ["otofacioosseous-gonadal syndrome", "Otofacioosseous-Gonadal Syndrome", "OTOFACIOOSSEOUS-GONADAL SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "otofacioosseous-gonadal syndrome", "shortest_name_length": 32}
{"curie": "MONDO:0033045", "names": ["OFD16", "Ofds 16", "OFDS XVI", "orofaciodigital syndrome 16", "orofaciodigital syndrome XVI", "OROFACIODIGITAL SYNDROME XVI", "oral-Facial-digital syndrome, type 16", "ORAL-FACIAL-DIGITAL SYNDROME, TYPE XVI"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orofaciodigital syndrome 16", "shortest_name_length": 5}
{"curie": "MONDO:0018820", "names": ["MECRCN", "TANGO2 deficiency", "TANGO2-related metabolic encephalopathy-arrhythmia syndrome", "TANGO2-related metabolic encephalopathy, arrhythmia syndrome", "transport and golgi organization protein 2 (TANGO2) deficiency", "METABOLIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION", "Transport and golgi organisation 2 homolog-related metabolic encephalopathy, arrhythmia syndrome", "Transport and golgi organization 2 homolog-related metabolic encephalopathy, arrhythmia syndrome", "metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration", "Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome", "recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome", "Recurrent metabolic encephalomyopathic crises, rhabdomyolysis, cardiac arrhythmia, intellectual disability syndrome", "Recurrent metabolic encephalomyopathic crises, rhabdomyolysis, cardiac arrhythmia, intellectual disability syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0007213", "names": ["Ballard syndrome", "Brachydactyly Ballard type", "brachydactyly Ballard type", "Ballard type brachydactyly", "PITT-WILLIAMS BRACHYDACTYLY", "Brachydactyly, Ballard Type", "BRACHYDACTYLY, BALLARD TYPE", "Pitt-Williams Brachydactyly", "Ballard syndrome (disorder)", "brachydactyly, Ballard type", "Pitt-Williams brachydactyly", "Pitt Williams brachydactyly", "brachydactyly combined B and E types", "brachydactyly types B and E combined", "Brachydactyly types B and E combined", "Brachydactyly, combined B and E types", "BRACHYDACTYLY, COMBINED B AND E TYPES", "brachydactyly, combined B and E types"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ballard syndrome", "shortest_name_length": 16}
{"curie": "UMLS:C0281707", "names": ["Stage IV Large Cell Lymphoma", "Stage IV Childhood Large Cell Lymphoma", "Childhood Large Cell Lymphoma Stage IV", "Pediatric Large Cell Lymphoma Stage IV", "stage IV childhood large cell lymphoma", "Stage IV Pediatric Large Cell Lymphoma", "stage IV large cell lymphoma, childhood", "lymphoma, stage IV childhood large cell", "pediatric large cell lymphoma, stage IV", "childhood large cell lymphoma, stage IV", "metastatic childhood large cell lymphoma", "large cell lymphoma, childhood, stage IV", "Metastatic Pediatric Large Cell Lymphoma", "childhood large cell lymphoma, metastatic", "metastatic large cell lymphoma, childhood", "lymphoma, metastatic childhood large cell", "pediatric large cell lymphoma, metastatic", "large cell lymphoma, childhood, metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Childhood Large Cell Lymphoma", "shortest_name_length": 28}
{"curie": "MONDO:0011191", "names": ["HCI", "capillary infantile hemangioma", "Hemangioma, capillary infantile", "HEMANGIOMA, CAPILLARY INFANTILE", "Hemangioma, hereditary capillary", "HEMANGIOMA, HEREDITARY CAPILLARY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "capillary infantile hemangioma", "shortest_name_length": 3}
{"curie": "UMLS:C4744587", "names": ["FTC, Widely Invasive", "Thyroid Gland Follicular Carcinoma, Widely Invasive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Follicular Carcinoma, Widely Invasive", "shortest_name_length": 20}
{"curie": "UMLS:C4520893", "names": ["Stage 0 Rectosigmoid Cancer", "Stage 0 Rectosigmoid Carcinoma", "Stage 0 Rectosigmoid Cancer AJCC v7", "Stage 0 Rectosigmoid Cancer AJCC v6", "Stage 0 Rectosigmoid Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Rectosigmoid Cancer AJCC v6 and v7", "shortest_name_length": 27}
{"curie": "UMLS:C0855113", "names": ["Diffuse Large B-Cell Lymphoma Stage I", "Diffuse large b-cell lymphoma stage I", "Stage I Diffuse Large B-Cell Lymphoma", "Diffuse large B-cell lymphoma stage I", "Diffuse non-Hodgkin's lymphoma Lugano stage I", "Diffuse non-Hodgkin's lymphoma Lugano stage 1", "Ann Arbor Stage I Diffuse Large B-Cell Lymphoma", "Diffuse non-Hodgkin's lymphoma Lugano stage I (disorder)", "Diffuse non-Hodgkin's lymphoma Lugano stage I (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Diffuse Large B-Cell Lymphoma", "shortest_name_length": 37}
{"curie": "UMLS:C3272834", "names": ["Colorectal Angiosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Angiosarcoma", "shortest_name_length": 23}
{"curie": "MONDO:0019634", "names": ["Familial nasal acilia", "familial nasal acilia", "Familial nasal acilia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial nasal acilia", "shortest_name_length": 21}
{"curie": "MONDO:0013774", "names": ["TRIGNO2", "trigonocephaly 2", "TRIGONOCEPHALY 2", "trigonocephaly type 2", "CRANIOSYNOSTOSIS, METOPIC", "craniosynostosis, metopic", "FREM1 isolated trigonocephaly", "isolated trigonocephaly caused by mutation in FREM1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trigonocephaly 2", "shortest_name_length": 7}
{"curie": "MONDO:0015686", "names": ["PPC", "EOPPC", "Primary Peritoneal Cancer", "primary peritoneal cancer", "Primary peritoneal carcinoma", "Primary Peritoneal Carcinoma", "primary peritoneal carcinoma", "serous surface papillary carcinoma", "primary peritoneal serous carcinoma", "primary peritoneal carcinoma (disease)", "Extra-ovarian primary peritoneal carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary peritoneal carcinoma", "shortest_name_length": 3}
{"curie": "MONDO:0000669", "names": ["color agnosia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "color agnosia", "shortest_name_length": 13}
{"curie": "MONDO:0012242", "names": ["VVS", "Familial vasovagal syncope", "familial vasovagal syncope", "syncope, familial VASOVAGAL", "SYNCOPE, FAMILIAL VASOVAGAL", "Syncope, familial vasovagal", "syncope, familial vasovagal", "Familial neurocardiogenic syncope", "syncope familial neurocardiogenic", "familial neurocardiogenic syncope", "Syncope, familial neurocardiogenic", "syncope, familial Neurocardiogenic", "SYNCOPE, FAMILIAL NEUROCARDIOGENIC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syncope, familial vasovagal", "shortest_name_length": 3}
{"curie": "MONDO:0003159", "names": ["PURPURA VASCULAR", "Palpable Purpura", "Vascular purpura", "Purpura vascular", "Vascular Purpura", "vascular purpura", "VASCULAR PURPURA", "vascular; purpura", "purpura; vascular", "Purpura, vascular", "hemostatic disorder", "Hemostatic Disorder", "Hemostatic Disorders", "Vascular hemostatic disease", "vascular hemostatic disease", "Vascular Hemostatic Diseases", "Vascular Hemostatic Disorder", "Vascular haemostatic disease", "vascular hemostatic disorder", "Hemostatic Disorder, Vascular", "vascular hemostatic disorders", "Disorder, Vascular Hemostatic", "Vascular Hemostatic Disorders", "hemostatic disorder, vascular", "disorder, vascular hemostatic", "hemostatic disorders, vascular", "Disorders, Vascular Hemostatic", "disorders, vascular hemostatic", "Hemostatic Disorders, Vascular", "Vascular hemostatic disease, NOS", "Vascular haemostatic disease, NOS", "Vascular hemostatic disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vascular hemostatic disease", "shortest_name_length": 16}
{"curie": "UMLS:C4683571", "names": ["Lugano Classification Stage II Bulky Adult Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage II Bulky Adult Lymphoma AJCC v8", "shortest_name_length": 59}
{"curie": "MONDO:0032824", "names": ["NEDBSS", "GPIBD21", "GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 21", "glycosylphosphatidylinositol biosynthesis defect 21", "NEURODEVELOPMENTAL DISORDER WITH BRAIN ANOMALIES, SEIZURES, AND SCOLIOSIS", "Neurodevelopmental Disorder With Brain Anomalies, Seizures, and Scoliosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycosylphosphatidylinositol biosynthesis defect 21", "shortest_name_length": 6}
{"curie": "UMLS:C0265581", "names": ["Radial clubhand", "Radial hemimelia", "Radial ray agenesis", "Radial longitidinal meromelia", "Longitudinal deficiency of radius", "longitudinal reduction defect; radius", "radius; longitudinal reduction defect", "Longitudinal deficiency of radius, NOS", "longitudinal reduction defect of radius", "Longitudinal reduction defect of radius", "Longitudinal deficiency of radius (disorder)", "congenital longitudinal reduction defect radius", "Congenital longitudinal deficiency of the radius", "longitudinal reduction defect of radius (diagnosis)", "Longitudinal reduction defect of unspecified radius"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Longitudinal deficiency of radius", "shortest_name_length": 15}
{"curie": "UMLS:C4682554", "names": ["Uterine Corpus Leiomyosarcoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Corpus Leiomyosarcoma by AJCC v8 Stage", "shortest_name_length": 46}
{"curie": "UMLS:C3897734", "names": ["Recurrent Olfactory Neuroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Olfactory Neuroblastoma", "shortest_name_length": 33}
{"curie": "UMLS:C1335453", "names": ["Base of Tongue Mucoepidermoid Carcinoma", "Posterior Tongue Mucoepidermoid Carcinoma", "Mucoepidermoid Carcinoma of Base of Tongue", "Base of the Tongue Mucoepidermoid Carcinoma", "Mucoepidermoid Carcinoma of Posterior Tongue", "Mucoepidermoid Carcinoma of the Posterior Tongue", "Mucoepidermoid Carcinoma of the Base of the Tongue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Posterior Tongue Mucoepidermoid Carcinoma", "shortest_name_length": 39}
{"curie": "MONDO:0014768", "names": ["CADASIL2", "CADASIL 2", "HTRA1 CADASIL", "CADASIL type 2", "CADASIL caused by mutation in HTRA1", "autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 2", "cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2", "CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2", "shortest_name_length": 8}
{"curie": "MONDO:0017602", "names": ["ALKoma", "ALK+ ALCL", "ALCL, ALK+", "ALK+ anaplastic large cell lymphoma", "ALK-Positive Anaplastic Large Cell Lymphoma", "ALK-positive anaplastic large cell lymphoma", "lymphoma anaplastic large cell alk-positive", "Anaplastic large cell lymphoma, ALK-positive", "Anaplastic large cell lymphoma, ALK positive", "anaplastic large cell lymphoma, ALK-positive", "Anaplastic Large Cell Lymphoma, ALK-Positive", "ALK-positive anaplastic large cell lymphoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ALK-positive anaplastic large cell lymphoma", "shortest_name_length": 6}
{"curie": "UMLS:C5206840", "names": ["Unresectable Oropharyngeal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Oropharyngeal Squamous Cell Carcinoma", "shortest_name_length": 50}
{"curie": "MONDO:0020377", "names": ["early-onset partial cataract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early-onset partial cataract", "shortest_name_length": 28}
{"curie": "MONDO:0009958", "names": ["RDPA", "HMSN4", "Refsum", "HMSN 4", "HMSN IV", "HSMN IV", "HMSN IVs", "HMSN type IV", "HMSN Type IV", "disease refsum", "REFSUM DISEASE", "Refsum disease", "refsum disease", "Refsum Disease", "refsums disease", "Refsums Disease", "refsum syndrome", "disease refsums", "Refsum Syndrome", "Refsum syndrome", "Disease, Refsum", "Refsum's Disease", "Refsums Syndrome", "refsum's disease", "Syndrome, Refsum", "disease refsum's", "Refsum's disease", "Disease, Refsum's", "Refsum's Syndrome", "refsum's syndrome", "Syndrome, Refsum's", "Adult Refsum Disease", "Adult Refsum disease", "adult Refsum disease", "Refsum Disease, Adult", "Disease, Adult Refsum", "Adult Refsum Diseases", "Refsum Diseases, Adult", "Classic Refsum disease", "classic Refsum disease", "Diseases, Adult Refsum", "Classic Refsum Disease", "Refsum-Thiebaut disease", "Disease, Classic Refsum", "Refsum disease, classic", "REFSUM DISEASE, CLASSIC", "Refsum-Thiébaut disease", "Classic Refsum Diseases", "Refsum Disease, Classic", "Refsum disease, adult, 1", "Refsum Thiebaut Syndrome", "Refsum Diseases, Classic", "REFSUM DISEASE, ADULT, 1", "Refsum-Thiebaut Syndrome", "Refsum Disease, Adult, 1", "Diseases, Classic Refsum", "Refsum-Thiebaut Syndromes", "Syndrome, Refsum-Thiebaut", "Syndromes, Refsum-Thiebaut", "DOC 11 (phytanic acid type)", "Refsum's disease (diagnosis)", "Phytanic Acid Storage Disease", "Phytanic acid storage disease", "Phytanic acid excess syndrome", "PHYTANIC ACID STORAGE DISEASE", "Phytanic Acid Oxidase Deficiency", "phytanic acid oxidase deficiency", "PHYTANIC ACID OXIDASE DEFICIENCY", "adult Refsum disease due to PHYH", "hypertrophic neuropathy of Refsum", "NEUROPATHY, HYPERTROPHIC OF REFSUM", "phytanic-CoA hydroxylase deficiency", "Phytanic-CoA hydroxylase deficiency", "Heredoataxic atactica polyneuritiformis", "Heredopathia atactica polyneuritiformis", "Heredopathia Atactica Polyneuritiformis", "heredopathia atactica polyneuritiformis", "HEREDOPATHIA ATACTICA POLYNEURITIFORMIS", "Phytanic acid storage disease (disorder)", "Polyneuritiformis, Heredopathia Atactica", "hereditary motor and sensory neuropathy 4", "Hereditary Motor And Sensory Neuropathy IV", "HEREDITARY MOTOR AND SENSORY NEUROPATHY IV", "Hemeralopia Heredoataxia Polyneuritiformis", "Heredoataxia hemeralopica polyneuritiformis", "Polyneuritiformis, Hemeralopia Heredoataxia", "Heredoataxia Polyneuritiformis, Hemeralopia", "Hereditary sensory-motor neuropathy, type 4", "Heredoataxic hemeralopica polyneuritiformis", "Hereditary sensory-motor neuropathy, type IV", "hereditary sensory and motor neuropathy type 4", "Hereditary motor and sensory neuropathy type 4", "hereditary motor and sensory neuropathy type 4", "Hereditary motor and sensory neuropathy type IV", "Hereditary Motor and Sensory Neuropathy Type IV", "Hereditary Type IV Motor and Sensory Neuropathy", "Hereditary motor and sensory neuropathy, type IV", "Refsum disease with increased pipecolic acidemia", "Hereditary Motor and Sensory Neuropathy, Type IV", "Neuropathy, Hereditary Motor and Sensory, Type IV", "disorder of cornification 11 (phytanic acid type)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult Refsum disease", "shortest_name_length": 4}
{"curie": "MONDO:0003348", "names": ["Classic Leiomyosarcoma", "classic leiomyosarcoma", "Conventional Leiomyosarcoma", "conventional leiomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "conventional leiomyosarcoma", "shortest_name_length": 22}
{"curie": "MONDO:0000383", "names": ["reproductive organ benign neoplasm", "Benign Reproductive System Neoplasm", "benign reproductive system neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign reproductive system neoplasm", "shortest_name_length": 34}
{"curie": "OMIM:111750", "names": [], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"]}
{"curie": "UMLS:C5236073", "names": ["Hereditary Colon Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hereditary Colon Carcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0013769", "names": ["AVSD5", "ATRIOVENTRICULAR SEPTAL DEFECT 5", "atrioventricular septal defect 5", "GATA6 atrioventricular septal defect", "atrioventricular septal defect type 5", "atrioventricular septal defect caused by mutation in GATA6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrioventricular septal defect 5", "shortest_name_length": 5}
{"curie": "UMLS:C1333378", "names": ["CNS PNET", "CNS Embryonal Tumor", "CNS Embryonal Neoplasm", "Embryonal Tumor of CNS", "Embryonal Neoplasm of CNS", "Embryonal Tumor of the CNS", "Embryonal Neoplasm of the CNS", "Central nervous system embryonal tumor", "Central Nervous System Embryonal Tumor", "Central Nervous System Embryonal Neoplasm", "Embryonal Tumor of Central Nervous System", "Embryonal Neoplasm of Central Nervous System", "Embryonal Tumor of the Central Nervous System", "Embryonal Neoplasm of the Central Nervous System", "Central nervous system primitive neuroectodermal tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Embryonal Neoplasm", "shortest_name_length": 8}
{"curie": "UMLS:C0948037", "names": ["CMV Gastroenteritis", "CMV gastroenteritis", "Cytomegalovirus gastroenteritis", "Cytomegalovirus Gastroenteritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cytomegalovirus gastroenteritis", "shortest_name_length": 19}
{"curie": "UMLS:C0341012", "names": ["Oral Herpes", "oral herpes", "Oral herpes", "herpes oral", "Herpes, Oral", "oral herpes simplex infection", "Oral herpes simplex infection", "Oral herpes simplex infection (disorder)", "oral herpes simplex infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral herpes simplex infection", "shortest_name_length": 11}
{"curie": "MONDO:0004473", "names": ["epiglottis cancer", "Epiglottic Cancer", "Epiglottic cancer", "epiglottic cancer", "Epiglottic carcinoma", "Epiglottic Carcinoma", "epiglottic carcinoma", "cancer of epiglottis", "epiglottic throat cancer", "Epiglottic Throat Cancer", "Malignant Epiglottic Tumor", "Malignant Epiglottis Tumor", "malignant epiglottic tumor", "malignant Epiglottis tumor", "EPIGLOTTIC CANCER MALIGNANT", "Malignant Epiglottis Neoplasm", "Malignant Tumor of Epiglottis", "malignant epiglottic neoplasm", "malignant tumor of Epiglottis", "malignant Epiglottis neoplasm", "Malignant Epiglottic Neoplasm", "malignant epiglottis neoplasm", "malignant neoplasm of Epiglottis", "malignant neoplasm of epiglottis", "Malignant Neoplasm of Epiglottis", "Malignant Tumor of the Epiglottis", "malignant tumor of the Epiglottis", "Malignant Neoplasm of the Epiglottis", "Malignant neoplasm of epiglottis NOS", "malignant neoplasm of the Epiglottis", "Malignant neoplasm of epiglottis, NOS", "Malignant neoplasm of anterior epiglottis", "malignant neoplasm of anterior epiglottis", "oropharyngeal neoplasm epiglottis, malignant", "malignant neoplasm of epiglottis (diagnosis)", "malignant tumor of anterior aspect of epiglottis", "malignant neoplasm of anterior aspect of epiglottis", "Malignant neoplasm of anterior aspect of epiglottis", "Malignant neoplasm of anterior surface of epiglottis", "malignant neoplasm of anterior surface of epiglottis", "Malignant neoplasm of anterior epiglottis (disorder)", "malignant neoplasm of anterior aspect of epiglottis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epiglottis cancer", "shortest_name_length": 17}
{"curie": "MONDO:0006827", "names": ["PICA syndrome", "Wallenberg syndrome", "WALLENBERG SYNDROME", "syndrome wallenberg", "wallenberg syndrome", "Wallenberg Syndrome", "Wallenbergs Syndrome", "Syndrome, Wallenberg", "wallenbergs syndrome", "wallenberg's syndrome", "Wallenberg's syndrome", "Wallenberg's Syndrome", "LATERAL BULBAR SYNDROME", "Lateral Bulbar Syndrome", "Vertebral artery syndrome", "lateral medullary syndrome", "Lateral Medullary Syndrome", "Lateral medullary syndrome", "LATERAL MEDULLARY SYNDROME", "Lateral Medullary Syndromes", "Vieseaux-Wallenberg Syndrome", "Vieseaux Wallenberg Syndrome", "Syndromes, Lateral Medullary", "VIEUSSEUX-WALLENBERG SYNDROME", "Syndrome, Vieseaux-Wallenberg", "Dorsolateral Medullary Syndrome", "Medullary Syndrome, Dorsolateral", "LMS - Lateral medullary syndrome", "Inferior cerebellar artery syndrome", "Posterior inferior cerebellar artery syndrome", "Posterior Inferior Cerebellar Artery Syndrome", "stroke of posterior inferior cerebellar artery", "Posterior inferior cerebellar artery syndrome (disorder)", "stroke of posterior inferior cerebellar artery (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lateral medullary syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0004054", "names": ["acute canaliculitis", "Acute canaliculitis", "lacrimal canaliculitis acute", "acute lacrimal canaliculitis", "Acute lacrimal canaliculitis", "Acute canaliculitis, lacrimal", "acute canaliculitis, lacrimal", "Acute lacrimal canaliculitis (disorder)", "acute lacrimal canaliculitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute canaliculitis", "shortest_name_length": 19}
{"curie": "MONDO:0023042", "names": ["ectodermal dysplasia margarita type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia margarita type", "shortest_name_length": 35}
{"curie": "UMLS:C4289955", "names": ["Atypical Endometriosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypical Endometriosis", "shortest_name_length": 22}
{"curie": "MONDO:0013461", "names": ["inosine triphosphatase deficiency", "Inosine Triphosphatase Deficiency", "INOSINE TRIPHOSPHATASE DEFICIENCY", "ITPase - Inosine triphosphatase deficiency", "inosine triphosphate pyrophosphohydrolase deficiency", "INOSINE TRIPHOSPHATE PYROPHOSPHOHYDROLASE DEFICIENCY", "Inosine triphosphate pyrophosphohydrolase deficiency", "Inosine triphosphate pyrophosphohydrolase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inosine triphosphatase deficiency", "shortest_name_length": 33}
{"curie": "MONDO:0009172", "names": ["Enterocolitis", "enterocolitis", "ENTEROCOLITIS", "Enterocolitides", "Enterocolitis, NOS", "enterocolitis (disease)", "enterocolitis (diagnosis)", "Inflammation of small intestine and colon", "Inflammation of small intestine and colon (disorder)", "Enterocolitis, inflammation involving both small intestine and colon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "enterocolitis", "shortest_name_length": 13}
{"curie": "UMLS:C0854964", "names": ["Recurrent Penis Cancer", "recurrent penile cancer", "penis cancer, recurrent", "Recurrent Penile Cancer", "penile cancer, recurrent", "Relapsed Penile Carcinoma", "Recurrent Penis Carcinoma", "Penis carcinoma recurrent", "Recurrent Penile Carcinoma", "Relapsed Carcinoma of Penis", "Recurrent Carcinoma of Penis", "Relapsed Carcinoma of the Penis", "Recurrent Carcinoma of the Penis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Penis carcinoma recurrent", "shortest_name_length": 22}
{"curie": "MONDO:0020322", "names": ["Mixed-Cell Leukemia", "Mixed-Cell Leukemias", "Leukemia, Mixed-Cell", "Leukemia, Mixed Cell", "Leukemias, Mixed-Cell", "Hybrid Acute Leukemia", "Hybrid Acute Leukemias", "Leukemia, Hybrid Acute", "Acute Leukemia, Hybrid", "Leukemias, Hybrid Acute", "Acute Leukemias, Hybrid", "Myeloid/lymphoid leukemia", "Myeloid/lymphoid leukaemia", "Acute Biphenotypic Leukemia", "acute biphenotypic leukemia", "Biphenotypic acute leukemia", "leukemia acute biphenotypic", "Biphenotypic Acute Leukemia", "Acute biphenotypic leukemia", "Leukemia, Biphenotypic Acute", "Biphenotypic Leukemia, Acute", "Acute Biphenotypic Leukemias", "Mixed-Lineage Acute Leukemia", "Biphenotypic Acute Leukemias", "Leukemia, Acute Biphenotypic", "Acute Leukemia, Biphenotypic", "Acute mixed lineage leukemia", "B and T Cell Leukemia, Acute", "Biphenotypic acute leukaemia", "B- and T-cell mixed leukemia", "Acute biphenotypic leukaemia", "Leukemia, Biphenotypic, Acute", "Leukemias, Biphenotypic Acute", "Leukemias, Acute Biphenotypic", "Leukemia, Mixed-Lineage Acute", "Acute Leukemias, Biphenotypic", "Acute Leukemia, Mixed-Lineage", "B- and T-Cell Leukemia, Acute", "Mixed-Lineage Acute Leukemias", "Leukemia, Mixed, B and T Cell", "Biphenotypic Leukemias, Acute", "Mixed Lineage Acute Leukemias", "mixed phenotype acute leukemia", "Leukemias, Mixed-Lineage Acute", "Leukemia, Mixed, B- and T-Cell", "Acute Leukemias, Mixed-Lineage", "Acute biphenotypic leukemia (disorder)", "acute biphenotypic leukemia (diagnosis)", "Leukemia, Lymphocytic, Acute, Mixed-Cell", "Leukemia, Lymphocytic, Acute, Mixed Cell", "B and T Cell Acute Lymphoblastic Leukemia", "Lymphocytic Leukemia, Acute, B and T Cell", "B- and T-Cell Acute Lymphoblastic Leukemia", "Lymphocytic Leukemia, Acute, B- and T-Cell", "Acute biphenotypic leukemia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute biphenotypic leukemia", "shortest_name_length": 19}
{"curie": "MONDO:0002930", "names": ["renal sarcoma", "Renal Sarcoma", "Renal sarcoma", "kidney sarcoma", "Kidney Sarcoma", "Sarcoma of Kidney", "sarcoma of kidney", "Sarcoma of kidney", "sarcoma of the kidney", "Sarcoma of the Kidney", "SARCOMA, RENAL, MALIGNANT", "Sarcoma of kidney (disorder)", "sarcoma of kidney (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kidney sarcoma", "shortest_name_length": 13}
{"curie": "OMIM:612556", "names": ["ADIPQTL1", "Hypoadiponectinemia", "HYPOADIPONECTINEMIA", "Adiponectin Deficiency", "ADIPONECTIN DEFICIENCY", "ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 8}
{"curie": "MONDO:0016740", "names": ["Choriocarcinoma of CNS", "choriocarcinoma of CNS", "choriocarcinoma of the CNS", "Choriocarcinoma of the CNS", "central nervous system choriocarcinoma", "Central Nervous System Choriocarcinoma", "Choriocarcinoma of the central nervous system", "choriocarcinoma of the central nervous system", "central nervous system choriocarcinoma (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choriocarcinoma of the central nervous system", "shortest_name_length": 22}
{"curie": "UMLS:C0948474", "names": ["Mycotic allergy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mycotic allergy", "shortest_name_length": 15}
{"curie": "MONDO:0002212", "names": ["pulmonary tularemia", "Tularemia pneumonia", "Pneumonia tularemia", "pneumonic tularemia", "Pulmonary tularemia", "Pneumonic tularemia", "Pulmonary tularaemia", "PNEUMONIA, TULAREMIC", "Tularaemia pneumonia", "pneumonic tularaemia", "Pneumonia tularaemia", "Pneumonic tularaemia", "Pneumonia in tularemia", "Pneumonia in tularaemia", "Pneumonia with tularemia", "Pneumonia with tularaemia", "bronchopneumonic tularemia", "TULAREMIA, PLEUROPULMONARY", "Bronchopneumonic tularemia", "Bronchopneumonic tularaemia", "Pulmonary tularemia (disorder)", "tularemia; pneumonia (etiology)", "pneumonia; tularemia (etiology)", "pulmonary tularemia (diagnosis)", "pneumonia; tularemia (manifestation)", "tularemia; pneumonia (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pneumonic tularemia", "shortest_name_length": 19}
{"curie": "UMLS:C5419179", "names": ["COVID-19-Associated Acute Digestive System Injury", "SARS-CoV-2-Associated Acute Digestive System Injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "COVID-19-Associated Acute Digestive System Injury", "shortest_name_length": 49}
{"curie": "MONDO:0004967", "names": ["ALL", "ALL1", "FAB L2", "ALL_TYPE", "lymphoid leukemia", "lymphocytic leukaemia", "leukemia lymphoblastic", "Lymphoblastic leukemia", "Lymphoblastic Lymphoma", "lymphoblastic leukemia", "Lymphoblastic Leukemia", "acute lymphoid leukemia", "Acute Lymphoid Leukemia", "Lymphoblastic leukaemia", "L2 Lymphocytic Leukemia", "lymphoblastic leukaemia", "Acute lymphoid leukemia", "Leukemia, Lymphoblastic", "Lymphoma, Lymphoblastic", "acute leukemia lymphoid", "Lymphocytic Leukemia, L2", "Acute lymphoid leukaemia", "Lymphoid Leukemia, Acute", "acute lymphatic leukemia", "Acute lymphatic leukemia", "Leukemia, L2 Lymphocytic", "Leukemia, Acute Lymphoid", "Lymphoid leukemia, acute", "acute lymphatic leukaemia", "Acute lymphatic leukaemia", "Leukemia, Lymphoid, Acute", "Lymphoid leukaemia, acute", "acute leukemia lymphocytic", "lymphatic; leukemia, acute", "lymphocytic leukemia acute", "ACUTE LYMPHOCYTIC LEUKEMIA", "[M]Acute lymphoid leukemia", "Acute Lymphocytic Leukemia", "acute lymphocytic leukemia", "Acute lymphocytic leukemia", "leukemia; lymphatic, acute", "Acute Lymphocytic Leukemias", "acute lymphogenous leukemia", "acute lymphocytic leukaemia", "leukemia, acute lymphocytic", "acute lymphocytic leukemias", "Acute Lymphogenous Leukemia", "Acute Lymphocytic Leukaemia", "Lymphocytic Leukemia, Acute", "[M]Acute lymphoid leukaemia", "Leukemias acute lymphocytic", "Leukaemia;acute lymphocytic", "Precursor lymphoid neoplasm", "Leukemia, Acute Lymphocytic", "Acute lymphocytic leukaemia", "Lymphoblastic leukemia, NOS", "LEUKEMIA, LYMPHOCYTIC, ACUTE", "acute lymphoblastic leukemia", "Leukaemias acute lymphocytic", "LEUKEMIA LYMPHOBLASTIC ACUTE", "acute leukemia lymphoblastic", "Acute Lymphoblastic Leukemia", "leukemia acute lymphoblastic", "Acute lymphoblastic leukemia", "ACUTE LYMPHOBLASTIC LEUKEMIA", "Leukemia lymphoblastic acute", "LEUKEMIA ACUTE LYMPHOBLASTIC", "Leukemia, Lymphocytic, Acute", "Lymphoblastic Leukemia, Acute", "Leukemia, Acute Lymphoblastic", "LEUKEMIA, ACUTE LYMPHOBLASTIC", "lymphoblastic leukemia, acute", "acute lymphoblastic leukaemia", "Acute lymphoblastic leukaemia", "Leukaemia lymphoblastic acute", "acute leukaemia lymphoblastic", "acute lymphoblastic leukemias", "LEUKEMIA, LYMPHOBLASTIC, ACUTE", "Leukemia, Lymphoblastic, Acute", "leukemia - acute lymphoblastic", "L2 Acute Lymphoblastic Leukemia", "precursor Lymphoblasic leukemia", "Precursor Lymphoblasic Leukemia", "Lymphoblastic leukemia, L2 type", "ALL - acute lymphocytic leukemia", "Acute lymphoid leukemia, disease", "ALL (acute lymphocytic leukemia)", "acute lymphocytic leukemia (ALL)", "precursor lymphoblastic leukemia", "ALL - Acute Lymphocytic Leukemia", "Leukemia, Lymphocytic, Acute, L2", "Acute lymphoid leukemia, L2 type", "Precursor Lymphoblastic Leukemia", "Lymphoblastic leukaemia, L2 type", "Acute lymphoblastic leukemia NOS", "Acute lymphoblastic leukemia, NOS", "Acute lymphoid leukaemia, L2 type", "Acute lymphoid leukaemia, disease", "Lymphoblastic Leukemia, Acute, L2", "Acute lymphoblastic leukaemia NOS", "Acute lymphatic leukemia, L2 type", "Acute lymphoblastic leukemia (ALL)", "LEUKEMIA, LYMPHOBLASTIC, MALIGNANT", "Acute lymphatic leukaemia, L2 type", "Leukemia, Lymphoblastic, Acute, L2", "acute lymphoblastic leukemia (ALL)", "ALL - Acute lymphoblastic leukemia", "Acute lymphoblastic leukemia [ALL]", "Acute Lymphoblastic Leukemia (ALL)", "leukemia, lymphoblastic, malignant", "Acute lymphocytic leukemia, L2 type", "ALL - Acute lymphoblastic leukaemia", "Lymphoblastic leukemia, NOS, L2 type", "Lymphoblastic Leukemia, Acute, Adult", "Acute lymphocytic leukaemia, L2 type", "Acute lymphoblastic leukemia-lymphoma", "Precursor cell lymphoblastic leukemia", "Lymphoblastic leukaemia, NOS, L2 type", "Acute lymphoblastic leukemia/lymphoma", "acute lymphoblastic leukemia/lymphoma", "leukemia precursor cell lymphoblastic", "Acute lymphoblastic leukemia, L2 type", "Precursor Cell Lymphoblastic Leukemia", "precursor cell lymphoblastic leukemia", "Acute lymphoblastic leukaemia-lymphoma", "acute lymphoblastic leukemia (disease)", "Precursor cell lymphoblastic leukaemia", "Acute lymphoblastic leukaemia, L2 type", "acute lymphocytic leukemia (diagnosis)", "precursor lymphoblastic lymphoma/leukemia", "Precursor cell lymphoblastic leukemia, NOS", "Acute lymphoblastic leukemia, L2 type, NOS", "Acute lymphoid leukemia, disease (disorder)", "Precursor Cell Lymphoblastic Leukemia Lymphoma", "Precursor Cell Lymphoblastic Leukemia-Lymphoma", "precursor cell lymphoblastic leukemia (diagnosis)", "Acute lymphoblastic leukemia, precursor cell type", "Acute lymphoblastic leukemia, precursor-cell type", "Acute lymphoblastic leukaemia, precursor-cell type", "Precursor cell lymphoblastic leukemia, not phenotyped", "Leukemia, Lymphoblastic, Acute, Philadelphia-Positive", "Precursor cell lymphoblastic leukaemia, not phenotyped", "Precursor cell lymphoblastic leukemia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute lymphoblastic leukemia", "shortest_name_length": 3}
{"curie": "UMLS:C0751888", "names": ["Midbrain Tumor", "midbrain tumor", "Tumor, Midbrain", "midbrain tumors", "Midbrain Tumors", "Tumors, Midbrain", "Midbrain Neoplasm", "Midbrain Neoplasms", "Neoplasm, Midbrain", "Neoplasms, Midbrain", "neoplasm of midbrain", "Mesencephalic Neoplasm", "Neoplasm, Mesencephalic", "Mesencephalic Neoplasms", "Neoplasms, Mesencephalic", "neoplasm of midbrain (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mesencephalic Neoplasms", "shortest_name_length": 14}
{"curie": "UMLS:C5206672", "names": ["Myointimoma", "Penile Myointimoma", "Myointimoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myointimoma", "shortest_name_length": 11}
{"curie": "MONDO:0044913", "names": ["eye metastasis", "EYE METASTASIS", "Eye Metastasis", "Metastasis to eye", "Metastases to eye", "Metastasis to Eye", "metastasis to eye", "Metastases to Eye", "Metastasis to the Eye", "Metastases to the Eye", "Metastases to the eye", "metastasis to the eye", "Metastatic Tumor to the Eye", "Metastatic tumor to the eye", "Metastatic Neoplasm to the Eye", "Metastatic neoplasm to the eye", "eye neoplasm malignant secondary", "Secondary malignant neoplasm of eye", "Metastatic malignant neoplasm to eye", "Metastatic malignant neoplasm of eye", "Metastatic malignant neoplasm to the eye", "Metastatic Malignant Neoplasm to the Eye", "Metastatic Malignant Neoplasm in the Eye", "Secondary malignant neoplasm of eye, NOS", "metastatic malignant neoplasm in the eye", "Metastatic malignant neoplasm in the eye", "Metastatic malignant neoplasm to eye, NOS", "Metastatic malignant neoplasm to eye (disorder)", "Secondary malignant neoplasm of eye (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metastatic malignant neoplasm in the eye", "shortest_name_length": 14}
{"curie": "UMLS:C1336193", "names": ["Stage IIB Ovarian Germ Cell Tumor", "Stage IIB Ovarian Germ Cell Tumor AJCC v6", "Stage IIB Ovarian Germ Cell Tumor AJCC v7", "FIGO Stage IIB Malignant Ovarian Germ Cell Tumor", "Stage IIB Ovarian Germ Cell Tumor AJCC v6 and v7", "FIGO Stage IIB Malignant Germ Cell Tumor of Ovary", "FIGO Stage IIB Malignant Ovarian Germ Cell Neoplasm", "FIGO Stage IIB Malignant Germ Cell Neoplasm of Ovary", "FIGO Stage IIB Malignant Germ Cell Tumor of the Ovary", "FIGO Stage IIB Malignant Germ Cell Neoplasm of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Ovarian Germ Cell Tumor AJCC v6 and v7", "shortest_name_length": 33}
{"curie": "UMLS:C0752109", "names": ["Inborn Metabolic Brain Diseases", "Inborn Metabolic Brain Disorders", "Metabolic Brain Diseases, Inborn", "Metabolic Brain Syndrome, Inborn", "Inborn Metabolic Disorders, Brain", "Brain Syndrome, Metabolic, Inborn", "Brain Diseases, Metabolic, Inborn", "Metabolic Diseases, Inborn, Brain", "Inborn Errors of Metabolism, Brain", "Encephalopathies, Metabolic, Inborn"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brain Diseases, Metabolic, Inborn", "shortest_name_length": 31}
{"curie": "MONDO:0002232", "names": ["nasal cavity disease", "Nasal Cavity Disease", "nasal cavity disorder", "Nasal Cavity Disorder", "cavity diseases nasal", "cavity disorders nasal", "disease of nasal cavity", "Disorder of nasal cavity", "disorder of nasal cavity", "nasal cavity disease or disorder", "nasal cavity disease (non-specific)", "disease or disorder of nasal cavity", "Disorder of nasal cavity (disorder)", "disorder of nasal cavity (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasal cavity disorder", "shortest_name_length": 20}
{"curie": "MONDO:0012577", "names": ["ASRT4", "ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 4", "asthma-related traits, susceptibility to, 4", "ASTHMA AND ALLERGIC RHINITIS, SUSCEPTIBILITY TO", "asthma and allergic rhinitis, susceptibility to", "asthma-related traits, susceptibility to, type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "asthma-related traits, susceptibility to, 4", "shortest_name_length": 5}
{"curie": "UMLS:C5557179", "names": ["Stage IIIC2 Cervical Cancer AJCC v9", "Stage IIIC2 Cervical Carcinoma AJCC v9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC2 Cervical Cancer AJCC v9", "shortest_name_length": 35}
{"curie": "UMLS:C0019816", "names": ["HSMN VII", "HMSN VII", "HMSN Type VII", "HMSN Type VIIs", "Type VII, HMSN", "Hereditary sensory-motor neuropathy, type 7", "Hereditary sensory-motor neuropathy, type VII", "Hereditary motor and sensory neuropathy type VII", "Hereditary motor and sensory neuropathy, type VII", "Hereditary, Type VII, Motor and Sensory Neuropathy", "Hereditary motor-sensory neuropathy with retinitis pigmentosa", "Hereditary sensory-motor neuropathy with retinitis pigmentosa", "Hereditary motor and sensory neuropathy with retinitis pigmentosa", "Hereditary motor and sensory neuropathy with retinitis pigmentosa (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hereditary, Type VII, Motor and Sensory Neuropathy", "shortest_name_length": 8}
{"curie": "UMLS:C4552221", "names": ["Vascular device infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vascular device infection", "shortest_name_length": 25}
{"curie": "MONDO:0009281", "names": ["GA1", "Ga 1", "GA I", "GCDHD", "Glutaric aciduria 1", "GLUTARIC ACIDURIA I", "Glutaric Aciduria I", "Glutaric acidemia 1", "glutaric acidemia I", "Glutaric Acidemia I", "glutaric aciduria 1", "GLUTARIC ACIDEMIA I", "glutaric acidemia 1", "glutaric academia type 1", "glutaricaciduria, type I", "Glutaric acidemia type I", "glutaric acidemia type I", "Glutaric Acidemia Type I", "Glutaric aciduria type I", "Glutaric acidemia type 1", "Glutaric aciduria type 1", "glutaric aciduria type 1", "Glutaric Acidemia Type 1", "glutaric aciduria type I", "glutaric acidemia type 1", "glutaric aciduria type i", "Glutaric Aciduria, Type 1", "glutaric aciduria, type 1", "Glutaric aciduria, type 1", "glutaric acidemia, type 1", "Glutaric acidemia, type 1", "Glutaric aciduria (type I)", "Glutaric acidaemia, type 1", "Glutaric aciduria, type 1 (disorder)", "GLUTARYL-CoA DEHYDROGENASE DEFICIENCY", "glutaryl-CoA dehydrogenase deficiency", "Glutaryl-CoA dehydrogenase deficiency", "glutaryl-coA dehydrogenase deficiency", "Glutaryl-coenzyme A dehydrogenase deficiency", "glutaryl-coenzyme A dehydrogenase deficiency", "glutaryl-CoA dehydrogenase deficiency (diagnosis)", "Glutaryl-coenzyme A dehydrogenase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glutaryl-CoA dehydrogenase deficiency", "shortest_name_length": 3}
{"curie": "MONDO:0020465", "names": ["congenital eyelid retraction", "Congenital eyelid retraction", "Congenital abnormal retraction of eyelid", "Congenital abnormal retraction of eyelid (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital eyelid retraction", "shortest_name_length": 28}
{"curie": "MONDO:0012875", "names": ["IBD21", "inflammatory bowel disease 21", "Inflammatory Bowel Disease 21", "INFLAMMATORY BOWEL DISEASE 21", "inflammatory bowel disease type 21"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory bowel disease 21", "shortest_name_length": 5}
{"curie": "MONDO:0013392", "names": ["SCAR10", "ANO10 autosomal recessive cerebellar ataxia", "autosomal recessive spinocerebellar ataxia 10", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 10", "spinocerebellar ataxia, autosomal recessive 10", "adult-onset autosomal recessive cerebellar ataxia", "Adult-onset autosomal recessive cerebellar ataxia", "autosomal recessive spinocerebellar ataxia type 10", "Autosomal recessive spinocerebellar ataxia type 10", "spinocerebellar ataxia, autosomal recessive type 10", "SCAR10 - autosomal recessive spinocerebellar ataxia type 10", "Adult-onset autosomal recessive cerebellar ataxia (disorder)", "autosomal recessive cerebellar ataxia caused by mutation in ANO10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive spinocerebellar ataxia 10", "shortest_name_length": 6}
{"curie": "MONDO:0015552", "names": ["DEB-ac", "DEB, acral", "Localized DEB, acral form", "Acral dystrophic epidermolysis bullosa", "acral dystrophic epidermolysis bullosa", "Acral DEB (dystrophic epidermolysis bullosa)", "Acral dystrophic epidermolysis bullosa (disorder)", "Localized dystrophic epidermolysis bullosa, acral form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acral dystrophic epidermolysis bullosa", "shortest_name_length": 6}
{"curie": "MONDO:0011066", "names": ["CMT4B", "CMT4B1", "CMT 4B", "CMT 4B1", "CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B", "Charcot-Marie-Tooth disease, Type 4B", "Charcot-Marie-Tooth disease type 4B1", "Charcot-Marie-Tooth disease Type 4B1", "Charcot Marie Tooth disease type 4B1", "Charcot-Marie-Tooth disease, type 4B", "Charcot-Marie-Tooth disease, Type 4B1", "Charcot-Marie-Tooth disease, type 4B1", "CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B1", "Charcot-Marie-Tooth neuropathy type 4B1", "Charcot-Marie-Tooth neuropathy, type 4B1", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4B1", "MTMR2 Charcot-Marie-Tooth disease type 4", "Charcot-Marie-Tooth Neuropathy, Type 4B1", "Charcot-Marie-Tooth disease type 4B1 (disorder)", "Charcot-Marie-Tooth disease Type 4B1 (diagnosis)", "Charcot-Marie-Tooth disease type 4 caused by mutation in MTMR2", "autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin sheaths type 4B1", "Charcot-Marie-Tooth disease, autosomal recessive, with focally folded myelin sheaths, autosomal recessive, type 4B1", "CHARCOT-MARIE-TOOTH DISEASE, AUTOSOMAL RECESSIVE, WITH FOCALLY FOLDED MYELIN SHEATHS, AUTOSOMAL RECESSIVE, TYPE 4B1", "Charcot-Marie-Tooth Disease, Autosomal Recessive, With Focally Folded Myelin Sheaths, Autosomal Recessive, Type 4b1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 4B1", "shortest_name_length": 5}
{"curie": "MONDO:0024538", "names": ["PFBC", "IBGC2", "BSPDC", "Fibgc", "IBGC1", "fahr disease", "Fahr disease", "Fahr syndrome", "Fahr's disease", "fahr's disease", "fahr's syndrome", "Fahr's syndrome", "IBGC3, FORMERLY", "IBGC2, FORMERLY", "Fahr disease, familial", "Fahr's syndrome (disorder)", "Fahr's syndrome (diagnosis)", "Striopallidodentate Calcinosis", "Cerebrovascular ferrocalcinosis", "cerebrovascular ferrocalcinosis", "ferrocalcinosis, cerebrovascular", "Cerebral symmetric calcification", "FAHR DISEASE, FAMILIAL, FORMERLY", "Ferrocalcinosis, Cerebrovascular", "FERROCALCINOSIS, CEREBROVASCULAR", "Fahr disease, familial, formerly", "PRIMARY FAMILIAL BRAIN CALCIFICATION", "Primary familial brain calcification", "Idiopathic basal ganglia calcification", "Bilateral striopallidodentate calcinosis", "Bilateral Striopallidodentate Calcinosis", "idiopathic basal ganglia calcification 1", "Idiopathic Basal Ganglia Calcification 1", "Idiopathic basal ganglia calcification 1", "STRIOPALLIDODENTATE CALCINOSIS, BILATERAL", "striopallidodentate calcinosis, bilateral", "Basal ganglia calcification, idiopathic 2", "Striopallidodentate Calcinosis, Bilateral", "basal ganglia calcification, idiopathic, 1", "basal ganglia calcification, idiopathic, 2", "Basal Ganglia Calcification, Idiopathic, 2", "BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1", "basal ganglia calcification, idiopathic, 3", "Basal Ganglia Calcification, Idiopathic, 1", "BSPDC Bilateral striopallidodentate calcinosis", "basal ganglia calcification, idiopathic, type 1", "Familial idiopathic basal ganglia calcification", "BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 3, FORMERLY", "basal ganglia calcification, idiopathic, 3, formerly", "BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 2, FORMERLY", "Idiopathic nonarteriosclerotic cerebrovascular calcification", "STRIOPALLIDODENTATE CALCINOSIS, AUTOSOMAL DOMINANT, ADULT-ONSET", "Striopallidodentate calcinosis, autosomal dominant, adult onset", "Striopallidodentate Calcinosis, Autosomal Dominant, Adult-Onset", "striopallidodentate calcinosis, autosomal dominant, adult-onset", "Adult-onset idiopathic nonarteriosclerotic cerebral calcification", "cerebral calcification, nonarteriosclerotic, idiopathic, adult-onset", "Cerebral Calcification, Nonarteriosclerotic, Idiopathic, Adult-Onset", "CEREBRAL CALCIFICATION, NONARTERIOSCLEROTIC, IDIOPATHIC, ADULT-ONSET"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "basal ganglia calcification, idiopathic, 1", "shortest_name_length": 4}
{"curie": "MONDO:0022519", "names": ["autoimmune myocarditis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune myocarditis", "shortest_name_length": 22}
{"curie": "UMLS:C4763939", "names": ["Non-infective Inflammatory Bowel Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-infective Inflammatory Bowel Disease", "shortest_name_length": 40}
{"curie": "UMLS:C4524710", "names": ["Clinical Stage 0 Gastroesophageal Junction Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage 0 Gastroesophageal Junction Adenocarcinoma AJCC v8", "shortest_name_length": 65}
{"curie": "UMLS:C1621719", "names": ["Lennert", "Lennert Lymphoma", "Lennert lymphoma", "lymphoma; Lennert", "lennerts lymphoma", "Lennert; lymphoma", "Lennert's Lymphoma", "Lennert's lymphoma", "Lymphoepithelioid lymphoma", "lymphoma lymphoepithelioid", "lymphoepithelioid; lymphoma", "lymphoma; lymphoepithelioid", "Lymphoepithelioid lymphoma (clinical)", "Lymphoepithelioid lymphoma (disorder)", "Lymphoepithelioid lymphoma (diagnosis)", "Lennert Variant Peripheral T-Cell Lymphoma", "Lennert's Variant Peripheral T-Cell Lymphoma", "Lymphoepithelioid lymphoma (morphologic abnormality)", "Lymphoepithelioid Variant Peripheral T-Cell Lymphoma", "Lymphoepithelioid Cell Variant Peripheral T-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoepithelioid lymphoma", "shortest_name_length": 7}
{"curie": "UMLS:C0948587", "names": ["Malignant nipple neoplasm male", "Male Malignant Nipple Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant nipple neoplasm male", "shortest_name_length": 30}
{"curie": "MONDO:0005797", "names": ["Slim disease", "Slim Disease", "slim disease", "disease; slim", "AIDS cachexia", "HIV Wasting Disease", "HIV wasting disease", "HIV WASTING SYNDROME", "HIV syndrome wasting", "wasting HIV syndrome", "Wasting Disease, HIV", "HIV Wasting Syndrome", "HIV wasting syndrome", "wasting syndrome HIV", "AIDS Wasting Syndrome", "AIDS wasting syndrome", "wasting syndrome aids", "Wasting Syndrome, HIV", "Wasting Syndrome, AIDS", "HIV disease; failure to thrive", "HIV disease resulting in wasting syndrome", "disease (or disorder); slim disease (HIV)", "HIV disease; resulting in, wasting syndrome", "HIV disease; resulting in, failure to thrive", "Acquired immunodeficiency syndrome wasting syndrome", "Human immunodeficiency virus infection wasting syndrome", "AIDS (acquired immunodeficiency syndrome) wasting syndrome", "Wasting syndrome due to acquired immunodeficiency syndrome", "HIV - Human immunodeficiency virus infection wasting syndrome", "Wasting syndrome due to acquired immunodeficiency syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HIV wasting syndrome", "shortest_name_length": 12}
{"curie": "UMLS:C1504534", "names": ["Radiation Burn", "Radiation burn", "radiation burn(s)", "burn from radiation", "Radiation burn (disorder)", "burn from radiation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radiation burn", "shortest_name_length": 14}
{"curie": "MONDO:0005579", "names": ["EIG", "EIG1", "generalized epilepsy", "generalised epilepsy", "Generalized epilepsy", "epilepsy generalized", "Generalised epilepsy", "Generalized Epilepsy", "epilepsy; generalized", "Epilepsy, Generalized", "Generalized Epilepsies", "GENERALIZED EPILEPSIES", "generalized; epileptic", "Epilepsies, Generalized", "generalized epilepsy nos", "Generalized epilepsy, NOS", "generalized seizure disorder", "Generalized Seizure Disorder", "SEIZURE DISORDER GENERALIZED", "Seizure Disorder, Generalized", "Generalized Seizure Disorders", "Seizure Disorders, Generalized", "epilepsy; syndrome, generalized", "Generalized epilepsy (disorder)", "idiopathic generalized epilepsy", "Epilepsy, Idiopathic Generalized", "epilepsy, idiopathic generalized", "generalized epilepsy (diagnosis)", "EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 1", "EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, LOCUS ON CHROMOSOME 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, idiopathic generalized", "shortest_name_length": 3}
{"curie": "MONDO:0011429", "names": ["JIA", "jra", "JRA", "JUVAR", "juvenile ra", "Juvenile RA", "Still's disease", "JUVENILE ARTHRITIS", "Juvenile arthritis", "Juvenile Arthritis", "Oligoarticular JRA", "Arthritis;juvenile", "juvenile arthritis", "ARTHRITIS JUVENILE", "Pauciarticular JRA", "juvenile; arthritis", "Arthritis, Juvenile", "Childhood Arthritis", "arthritis; juvenile", "Childhood arthritis", "Arthritis, Childhood", "Childhood Arthritides", "Arthritides, Childhood", "juvenile chronic arthritis", "Juvenile chronic arthritis", "Juvenile Chronic Arthritis", "Chronic Arthritis, Juvenile", "Arthritis, Juvenile Chronic", "Oligoarticular Still Disease", "idiopathic juvenile arthritis", "Juvenile idiopathic arthritis", "juvenile idiopathic arthritis", "Juvenile Rheumatoid Arthritis", "JUVENILE RHEUMATOID ARTHRITIS", "ARTHRITIS RHEUMATOID JUVENILE", "Juvenile rheumatoid arthritis", "children rheumatoid arthritis", "Juvenile Idiopathic Arthritis", "juvenile rheumatoid arthritis", "Oligoarticular Still's Disease", "juvenile arthritis (diagnosis)", "juvenile chronic polyarthritis", "Rheumatoid Arthritis, Juvenile", "Arthritis, Juvenile Rheumatoid", "Arthritis, Juvenile Idiopathic", "Idiopathic Arthritis, Juvenile", "Rheumatoid arthritis, juvenile", "Juvenile arthritis, unspecified", "arthritis; rheumatoid, juvenile", "Juvenile seropositive arthritis", "juvenile; arthritis, rheumatoid", "arthritis; juvenile, rheumatoid", "ARTHRITIS, RHEUMATOID, JUVENILE", "Rheumatoid arthritis in children", "rheumatoid arthritis in children", "JCA - Juvenile chronic arthritis", "Juvenile rheumatoid arthritis NOS", "Pauciarticular juvenile arthritis", "pauciarticular juvenile arthritis", "Pauciarticular juvenile chronic RA", "Juvenile rheumatoid arthritis, NOS", "acute juvenile rheumatoid arthritis", "Acute juvenile rheumatoid arthritis", "arthritis; juvenile, pauciarticular", "JRA - Juvenile rheumatoid arthritis", "JIA - juvenile idiopathic arthritis", "juvenile; arthritis, pauciarticular", "systemic juvenile rheumatoid arthritis", "Pauciarticular onset juvenile arthritis", "rheumatoid arthritis, systemic juvenile", "Juvenile idiopathic arthritis (disorder)", "juvenile idiopathic arthritis (diagnosis)", "Unspecified juvenile rheumatoid arthritis", "monarticular juvenile rheumatoid arthritis", "monoarticular juvenile idiopathic arthritis", "Monoarticular juvenile rheumatoid arthritis", "Oligoarticular Juvenile Rheumatoid Arthritis", "Pauciarticular juvenile rheumatoid arthritis", "juvenile idiopathic arthritis, monoarticular", "pauciarticular onset juvenile chronic arthritis", "Pauciarticular onset juvenile chronic arthritis", "Acute polyarticular juvenile rheumatoid arthritis", "acute polyarticular juvenile idiopathic arthritis", "Acute polyarticular juvenile idiopathic arthritis", "Pauciarticular Juvenile Rheumatoid Arthritis (AQ)", "Polyarticular juvenile rheumatoid arthritis, acute", "Pauciarticular juvenile arthritis, site unspecified", "JCA - Pauciarticular onset juvenile chronic arthritis", "monoarticular juvenile idiopathic arthritis (diagnosis)", "rheumatoid arthritis, systemic juvenile, susceptibility to", "Acute polyarticular juvenile idiopathic arthritis (disorder)", "acute polyarticular juvenile idiopathic arthritis (diagnosis)", "Pauciarticular juvenile rheumatoid arthritis, unspecified site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile idiopathic arthritis", "shortest_name_length": 3}
{"curie": "MONDO:0024507", "names": ["AN", "AN1", "aniridia", "ANIRIDIA 1", "aniridia 1", "aniridia II", "AN2, FORMERLY", "Aniridia type 1", "aniridia II, formerly", "ANIRIDIA II, FORMERLY", "Aniridia type 1 (disorder)", "Aniridia type 1 (diagnosis)", "cataract with late-onset corneal dystrophy", "cataract, congenital, with late-onset corneal dystrophy", "CATARACT, CONGENITAL, WITH LATE-ONSET CORNEAL DYSTROPHY", "CATARACTS, CONGENITAL, WITH LATE-ONSET CORNEAL DYSTROPHY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aniridia 1", "shortest_name_length": 2}
{"curie": "UMLS:C0239211", "names": ["EAR EDEMA", "Edema auricular", "Oedema auricular"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Edema auricular", "shortest_name_length": 9}
{"curie": "UMLS:C0935805", "names": ["Stage I Merkel Cell Cancer", "Stage I Merkel Cell Carcinoma", "stage I Merkel cell carcinoma", "Merkel cell carcinoma, stage I", "Stage I Merkel Cell Carcinoma AJCC v7", "stage I neuroendocrine carcinoma of the skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Merkel Cell Carcinoma AJCC v7", "shortest_name_length": 26}
{"curie": "MONDO:0025478", "names": ["Veterinary Venereal Tumor", "veterinary venereal tumor", "tumor, veterinary venereal", "Tumor, Veterinary Venereal", "venereal tumor, veterinary", "Venereal Tumor, Veterinary", "Veterinary Venereal Tumors", "veterinary venereal tumors", "venereal tumors, veterinary", "Venereal Tumors, Veterinary", "Tumors, Veterinary Venereal", "tumors, veterinary venereal", "Transmissible Venereal Tumor", "transmissible venereal tumor", "Tumor, Transmissible Venereal", "Transmissible Venereal Tumors", "tumor, transmissible venereal", "Venereal Tumor, Transmissible", "venereal tumor, transmissible", "transmissible venereal tumors", "venereal tumors transmissible", "Venereal Tumors, Transmissible", "venereal tumors, transmissible", "tumors, transmissible venereal", "Tumors, Transmissible Venereal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "venereal tumors, veterinary", "shortest_name_length": 25}
{"curie": "MONDO:0019151", "names": ["Oligocone syndrome", "oligocone trichromacy", "Oligocone trichromacy", "Oligocone trichromacy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oligocone trichromacy", "shortest_name_length": 18}
{"curie": "UMLS:C5446517", "names": ["Unresectable Vaginal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Vaginal Carcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0044344", "names": ["Katayama", "Katamaya fever", "Katayama Fever", "Katayama fever", "YANGTZE DISEASE", "fever; Katayama", "Katayama; fever", "Katayama disease", "KATAYAMA DISEASE", "Katamaya syndrome", "Katayama syndrome", "YANGTZE RIVER DISEASE", "acute schistosomiasis", "Schistosoma; japonicum", "Asian; schistosomiasis", "Asiatic schistosomiasis", "eastern schistosomiasis", "schistosomiasis; eastern", "schistosomiasis; Asiatic", "Asiatic; schistosomiasis", "eastern; schistosomiasis", "SCHISTOSOMIASIS, EASTERN", "SCHISTOSOMIASIS JAPONICA", "Schistosomiasis japonica", "Katayama disease or fever", "Schistosomiasis japonicum", "schistosomiasis japonicum", "schistosomiasis; oriental", "oriental; schistosomiasis", "Katayama fever (diagnosis)", "Asiatic schistosomiasis NOS", "Schistosoma Japonicum Infection", "Schistosoma japonicum infection", "Schistosoma japonicum Infection", "Schistosoma japonicum Infections", "Infection, Schistosoma japonicum", "Infections, Schistosoma japonicum", "infestation; Schistosoma, japonicum", "Schistosoma; infestation, japonicum", "schistosomiasis; Schistosoma japonicum", "Schistosoma japonicum infectious disease", "Schistosoma japonicum disease or disorder", "Schistosoma japonicum infection (disorder)", "Schistosomiasis due to schistosoma japonicum", "schistosomiasis due to Schistosoma japonicum", "Schistosomiasis due to Schistosoma japonicum", "Schistosoma japonicum caused disease or disorder", "schistosomiasis due to Schistosoma japonicum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Schistosoma japonicum infectious disease", "shortest_name_length": 8}
{"curie": "UMLS:C5418760", "names": ["Appendix Mucinous Tumor", "Appendix Mucinous Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Appendix Mucinous Neoplasm", "shortest_name_length": 23}
{"curie": "MONDO:0002072", "names": ["MNTI", "Melanomeloblastoma", "Melanotic progonoma", "melanotic Progonoma", "melanoameloblastoma", "Melanotic Progonoma", "Melanoameloblastoma", "Melanoameloblastomas", "Melanotic Progonomas", "Retinal anlage tumor", "Progonoma, Melanotic", "Retinal Anlage Tumor", "Anlage Tumor, Retinal", "Progonomas, Melanotic", "Retinal anlage tumour", "Tumor, Retinal Anlage", "Retinal Anlage Tumors", "Tumors, Retinal Anlage", "Anlage Tumors, Retinal", "Retinal Anlage Neoplasm", "retinal anlage neoplasm", "Melanotic progonoma of skin", "Melanotic neuroectodermal tumor", "pigmented neuroectodermal tumor", "Melanotic Neuroectodermal Tumor", "Pigmented Neuroectodermal Tumor", "melanotic neuroectodermal tumor", "Melanotic Neuroectodermal Tumors", "Neuroectodermal Tumor, Melanotic", "melanotic neuroectodermal tumour", "Melanotic neuroectodermal tumour", "Tumor, Melanotic Neuroectodermal", "Neuroectodermal Tumors, Melanotic", "Tumors, Melanotic Neuroectodermal", "Melanotic Neuroectodermal Tumor of Infancy", "Melanotic neuroectodermal tumor of infancy", "Pigmented neuroectodermal tumor of infancy", "melanotic neuroectodermal tumor of infancy", "Melanotic neuroectodermal tumour of infancy", "Pigmented neuroectodermal tumour of infancy", "pigmented neuroectodermal tumour of infancy", "infantile melanotic neuroectodermal neoplasm", "Infantile Melanotic neuroectodermal neoplasm", "Infantile Melanotic Neuroectodermal Neoplasm", "MNTI-melanotic neuroectodermal tumour of infancy", "MNTI - melanotic neuroectodermal tumor of infancy", "MNTI - melanotic neuroectodermal tumour of infancy", "Melanotic neuroectodermal tumor of infancy (disorder)", "Pigmented neuroectodermal tumor of infancy (disorder)", "Melanotic neuroectodermal tumor (morphologic abnormality)", "melanotic neuroectodermal tumor (morphologic abnormality)", "melanotic neuroectodermal tumor of infancy (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melanotic neuroectodermal tumor", "shortest_name_length": 4}
{"curie": "MONDO:0005030", "names": ["iugr", "IUGR", "iugrs", "fetal SGA", "Fetal SGA", "Small baby", "Microsomia", "baby small", "microsomia", "babies small", "baby date small", "Microsomic baby", "Poor fetal growth", "poor fetal growth", "poor; fetal growth", "slow; fetal growth", "Poor foetal growth", "fetal; poor growth", "fetal; slow growth", "babies dates small", "Poor prenatal growth", "Small for dates baby", "Small-for-dates baby", "SMALL FOR DATES BABY", "Poor fetal growth state", "Prenatal growth failure", "Fetal growth restriction", "Fetal Growth Restriction", "prenatal growth disorder", "fetal growth restriction", "Poor foetal growth state", "Intrauterine retardation", "Fetal Growth Retardation", "Fetal growth retardation", "fetal growth retardation", "fetal Growth retardation", "Foetal growth restriction", "intrauterine; retardation", "retardation; intrauterine", "fetal; growth retardation", "Foetal growth retardation", "intrauterine growth retard", "SFD - Small-for-dates baby", "Growth intrauterine retard", "Intrauterine growth retard", "Prenatal growth deficiency", "Small-for-dates - delivered", "In utero growth retardation", "Prenatal growth retardation", "Intrauterine growth failure", "age babies gestational small", "Fetal growth retardation, NOS", "intrauterine growth retardatio", "FGR - Fetal growth retardation", "Intrauterine growth retardatio", "small for gestational age baby", "Small for gestational age baby", "Small baby for gestational age", "Slow fetal growth, unspecified", "Foetal growth retardation, NOS", "intrauterine Growth retardation", "Small-for-dates baby (disorder)", "fetus small for gestational Age", "Intrauterine Growth Retardation", "FGR - Foetal growth retardation", "intrauterine Growth restriction", "growth intrauterine retardation", "Intrauterine growth restriction", "Fetal Small for Gestational Age", "fetal small for gestational Age", "INTRAUTERINE GROWTH RETARDATION", "intrauterine growth restriction", "Intrauterine Growth Restriction", "growth intrauterine restriction", "intrauterine growth retardation", "Intrauterine growth retardation", "Fetus Small for Gestational Age", "Growth Retardation, Intrauterine", "infant small for gestational age", "Small for gestational age infant", "Infant, Small for Gestational Age", "Prenatal-onset growth retardation", "Prenatal onset growth retardation", "Growth retardation, prenatal onset", "Fetal growth retardation (disorder)", "Intrauterine growth retardation, NOS", "Intrauterine growth retardation, IUGR", "Fetal growth retardation, unspecified", "IUGR - Intrauterine growth retardation", "Foetal growth retardation, unspecified", "Intrauterine growth retardation (IUGR)", "intrauterine growth retardation (diagnosis)", "Fetal growth retardation, unspecified weight", "Fetal growth retardation, unspecified {weight}", "Fetal growth retardation, unspecified [weight]", "Foetal growth retardation, unspecified {weight}", "Fetal growth retardation, unspecified, unspecified [weight]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fetal growth restriction", "shortest_name_length": 4}
{"curie": "MONDO:0006031", "names": ["CHRONIC SINUSITIS", "chronic sinusitis", "Sinusitis;chronic", "SINUSITIS CHRONIC", "Chronic Sinusitis", "Chronic sinusitis", "sinusitis chronic", "Sinusitis, chronic", "sinusitis, chronic", "chronics sinusitis", "Sinusitis chronic NOS", "SINUS DISEASE CHRONIC", "Chronic sinus disease", "Chronic sinusitis NOS", "Chronic rhinosinusitis", "Chronic sinusitis, NOS", "chronic rhinosinusitis", "rhinosinusitis chronic", "chronic sinus infection", "sinus infection chronic", "Sinusitis (chronic) NOS", "chronic infection sinus", "chronic infections sinus", "Chronic infection of sinus", "Chronic sinusitis (disorder)", "Chronic unspecified sinusitis", "chronic sinusitis (diagnosis)", "Chronic sinusitis, unspecified", "Unspecified sinusitis (chronic)", "Chronic infection of sinus, NOS", "Chronic rhinosinusitis (disorder)", "Chronic rhinosinusitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic rhinosinusitis", "shortest_name_length": 17}
{"curie": "MONDO:0005954", "names": ["Screw Worm Myiasis", "Screw Worm Myiases", "Myiases, Screw Worm", "Myiasis, Screw Worm", "Screw Worm Infection", "infection, screw worm", "Screw Worm Infections", "screw worm infections", "Infection, Screw Worm", "infections, screw worm", "screw worm infectious disease", "Cochliomyia hominivorax infectious disease", "Cochliomyia hominivorax disease or disorder", "Cochliomyia hominivorax caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "screw worm infectious disease", "shortest_name_length": 18}
{"curie": "MONDO:0009702", "names": ["MYOPATHY DUE TO MALATE-ASPARTATE SHUTTLE DEFECT", "myopathy due to malate-aspartate shuttle defect", "Myopathy due to Malate-Aspartate Shuttle Defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy due to malate-aspartate shuttle defect", "shortest_name_length": 47}
{"curie": "MONDO:0004772", "names": ["Terrien-Viel syndrome", "glaucomatocyclitic crisis", "glaucomatocyclitic crises", "Glaucomatocyclitic crises", "Glaucomatocyclitic crisis", "Posner-Schlossman syndrome", "crisis; glaucomatocyclitic", "posner schlossman syndrome", "posner-schlossman syndrome", "glaucomatocyclitic; crisis", "Glaucomatocyclitic crisis (disorder)", "glaucomatocyclitic crises (diagnosis)", "Benign paroxysmal ocular hypertension syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glaucomatocyclitic crisis", "shortest_name_length": 21}
{"curie": "MONDO:0020296", "names": ["av fistula", "AV fistula", "AV Fistula", "AV FISTULA", "a-v fistula", "av fistulas", "a v fistula", "a v fistulas", "XXX>AV fistula", "Arteriovenous shunt", "arteriovenous shunt", "arteriovenous fistula", "Fistula;arteriovenous", "fistula arteriovenous", "FISTULA ARTERIOVENOUS", "Fistula arteriovenous", "Pathologic AV Fistula", "Arteriovenous Fistula", "Arteriovenous fistula", "arteriovenous fistulas", "arterio-venous fistula", "FISTULA, ARTERIOVENOUS", "Fistula, Arteriovenous", "Arteriovenous fistulas", "fistulas arteriovenous", "Arteriovenous Fistulas", "fistula; arteriovenous", "arteriovenous; fistula", "arteriovenous aneurysm", "Fistulas, Arteriovenous", "arteriovenous av fistula", "AV - Arteriovenous fistula", "congenital arteriovenous shunt", "Arteriovenous fistula (disorder)", "Congenital arteriovenous fistula", "Congenital Arteriovenous Fistula", "congenital arteriovenous fistula", "Pathologic Arteriovenous Fistula", "arteriovenous fistula (diagnosis)", "Arteriovenous fistula, congenital", "Congenital arteriovenous fistula, NOS", "Congenital AV - arteriovenous fistula", "Congenital arteriovenous fistula - disorder", "Congenital arteriovenous fistula (disorder)", "congenital arteriovenous fistula (diagnosis)", "Arteriovenous fistula (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital arteriovenous fistula", "shortest_name_length": 10}
{"curie": "UMLS:C3897721", "names": ["Remote Placental Infarct", "Remote Placental Infarction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Remote Placental Infarction", "shortest_name_length": 24}
{"curie": "UMLS:C0161022", "names": ["genitourinary; foreign body", "Foreign body in urogenital tract", "foreign body; genitourinary tract", "foreign body of genitourinary tract", "Foreign Body in Genitourinary Tract", "Foreign body in genitourinary tract", "Foreign body in genitourinary tract, NOS", "Foreign body in genitourinary tract (disorder)", "foreign body of genitourinary tract (diagnosis)", "Foreign body in genitourinary tract, part unspecified", "Foreign body in unspecified site in genitourinary tract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Foreign body in genitourinary tract", "shortest_name_length": 27}
{"curie": "MONDO:0007565", "names": ["CYLD", "Turban Tumor", "turban tumor", "Turban tumor", "Turban tumour", "turban; tumor", "Turban tumors", "tumors turban", "turban tumors", "tumor; turban", "cylindromas dermal", "Turban tumor syndrome", "turban tumor syndrome", "Turban Tumor Syndrome", "'TURBAN TUMOR' SYNDROME", "'turban tumor' syndrome", "Ancell-Spiegler syndrome", "Ancell-Spiegler Syndrome", "Familial cylindromatosis", "familial cylindromatosis", "Cylindromatosis, familial", "Dermal Eccrine Cylindroma", "cylindromatosis, familial", "CYLINDROMATOSIS, FAMILIAL", "Familial Trichoepithelioma", "Ancell-Spiegler cylindromas", "ANCELL-SPIEGLER CYLINDROMAS", "CYLINDROMAS, DERMAL ECCRINE", "Ancell-Spiegler Cylindromas", "Cylindromas, dermal eccrine", "Cylindromas, Dermal Eccrine", "turban tumor (physical finding)", "Turban tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial cylindromatosis", "shortest_name_length": 4}
{"curie": "MONDO:0024345", "names": ["pityriasis streptogenes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pityriasis streptogenes", "shortest_name_length": 23}
{"curie": "MONDO:0008238", "names": ["ACP3--ALPHA POLYPEPTIDE", "Acp3--Alpha polypeptide", "LYSOSOMAL ACID PHOSPHATASE", "lysosomal acid phosphatase", "phosphatase, acid, of tissues", "PHOSPHATASE, ACID, OF TISSUES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phosphatase, acid, of tissues", "shortest_name_length": 23}
{"curie": "MONDO:0014510", "names": ["PFCRD", "FAR1 deficiency", "fatty acyl-CoA reductase 1 disorder", "fatty acyl-CoA reductase 1 deficiency", "Fatty acyl-CoA reductase 1 deficiency", "rhizomelic chondrodysplasia punctata type 4", "rhizomelic chondrodysplasia punctate type 4", "Fatty acyl-coenzyme A reductase 1 deficiency", "peroxisomal fatty acyl-CoA reductase 1 disorder", "PEROXISOMAL FATTY ACYL-CoA REDUCTASE 1 DISORDER", "Peroxisomal fatty acyl-CoA reductase 1 disorder", "PFCRD - peroxisomal fatty acyl-CoA reductase 1 disorder", "Fatty acyl-coenzyme A reductase 1 deficiency (disorder)", "fatty acyl-CoA reductase 1 disorder or fatty acyl-CoA reductase 1 deficiency", "severe intellectual disability-epilepsy-cataract syndrome due to FAR1 deficiency", "severe intellectual disability-epilepsy-cataract syndrome due to peroxisomal disorder", "severe intellectual disability-epilepsy-cataract syndrome due to fatty acyl-CoA reductase 1 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fatty acyl-CoA reductase 1 deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0006998", "names": ["Tonsil Tumor", "tonsil tumor", "cancer tonsil", "Tonsil Cancer", "tonsil tumors", "Tonsil cancer", "tonsil cancer", "cancer tonsils", "Tonsil Cancers", "Cancer, Tonsil", "tonsils tumors", "Cancers, Tonsil", "Tonsillar Tumor", "Tonsil Neoplasm", "Tumor of Tonsil", "Tonsils--Cancer", "Tumor of tonsil", "Neoplasm, Tonsil", "Tonsillar Cancer", "cancer of tonsil", "Tonsil Neoplasms", "Cancer of Tonsil", "Tumour of tonsil", "Cancer of tonsil", "tonsillar cancer", "of tonsil cancer", "Neoplasms, Tonsil", "Tonsillar Cancers", "Cancer, Tonsillar", "Neoplasm of Tonsil", "Tonsillar Neoplasm", "tonsillar neoplasm", "Cancers, Tonsillar", "neoplasm of tonsil", "Tonsillar neoplasm", "Tonsillar Neoplasms", "Tumor of the Tonsil", "tonsillar neoplasms", "Neoplasm, Tonsillar", "Neoplasms, Tonsillar", "Cancer of the Tonsil", "cancer of the tonsil", "CA - Cancer of tonsil", "Malignant Tonsil Tumor", "Tonsillar neoplasm NOS", "Neoplasm of the Tonsil", "malignant tonsil tumor", "malignant tonsil neoplasm", "malignant Tonsillar tumor", "Malignant tumor of tonsil", "Malignant Tumor of Tonsil", "Malignant neoplasm tonsil", "Malignant Tonsil Neoplasm", "malignant tonsillar tumor", "malignant tumor of tonsil", "Malignant Tonsillar Tumor", "Malignant tumour of tonsil", "Malignant Tonsillar Neoplasm", "Malignant neoplasm of tonsil", "Malignant Neoplasm of Tonsil", "malignant neoplasm of tonsil", "malignant tonsillar neoplasm", "malignant tumor of the tonsil", "Malignant Tumor of the Tonsil", "neoplasm of tonsil (diagnosis)", "Malignant neoplasm of tonsil NOS", "malignant neoplasm of the tonsil", "Malignant Neoplasm of the Tonsil", "Malignant neoplasm of tonsil, NOS", "Malignant tumor of faucial tonsil", "Malignant tumor of palatine tonsil", "Malignant tumour of faucial tonsil", "Malignant tumour of palatine tonsil", "Malignant neoplasm of faucial tonsil", "Malignant tumor of tonsil (disorder)", "malignant neoplasm of faucial tonsil", "malignant neoplasm of tonsil, faucial", "malignant neoplasm of palatine tonsil", "Malignant neoplasm of palatine tonsil", "Malignant neoplasm of faucial tonsils", "Malignant neoplasm of tonsil, faucial", "Malignant neoplasm of palatine tonsils", "Malignant neoplasm of tonsil, palatine", "malignant neoplasm of tonsil (diagnosis)", "Malignant neoplasm of tonsil, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tonsil cancer", "shortest_name_length": 12}
{"curie": "MONDO:0020766", "names": ["CHN3", "hypomyelinating neuropathy, congenital, 3", "neuropathy, congenital hypomyelinating, 3", "NEUROPATHY, CONGENITAL HYPOMYELINATING, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuropathy, congenital hypomyelinating, 3", "shortest_name_length": 4}
{"curie": "MONDO:0013125", "names": ["CLAPO", "Clapo", "CLAPO Syndrome", "CLAPO syndrome", "CLAPO syndrome, somatic", "Lopez-Gutierrez Syndrome", "Lopez-Gutierrez syndrome", "LOPEZ-GUTIERREZ SYNDROME", "Capillary malformation of lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs and overgrowth syndrome", "CLAPO (capillary malformation of lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs and overgrowth) syndrome", "Capillary malformation of lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs and overgrowth syndrome (disorder)", "Capillary Malformation Of The Lower Lip, Lymphatic Malformation Of Face And Neck, Asymmetry Of Face And Limbs, And Partial-Generalized Overgrowth", "capillary malformation of the LOWER LIP, lymphatic malformation of face and neck, asymmetry of face and limbs, and partial/generalized overgrowth", "CAPILLARY MALFORMATION OF THE LOWER LIP, LYMPHATIC MALFORMATION OF FACE AND NECK, ASYMMETRY OF FACE AND LIMBS, AND PARTIAL/GENERALIZED OVERGROWTH"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CLAPO syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C5237249", "names": ["Unresectable Mucosal Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Mucosal Melanoma", "shortest_name_length": 29}
{"curie": "UMLS:C0006852", "names": ["Vaginal thrush", "vaginal thrush", "thrush vaginal", "Thrush vaginal", "Yeast vaginitis", "Candida vaginal", "Vaginal candida", "candida vaginal", "vaginal candida", "yeast vaginitis", "VAGINITIS, YEAST", "Candida of vagina", "candida vaginitis", "VAGINITIS CANDIDA", "vaginitis candida", "candidiasis vagina", "VAGINITIS, CANDIDA", "vaginal moniliasis", "MONILIASIS VAGINAL", "VAGINAL MONILIASIS", "Monilial Vaginitis", "vaginal candidosis", "Vaginal moniliasis", "VAGINITIS MONILIAL", "Moniliasis vaginal", "Vaginitis;monilial", "candidosis vaginal", "monilial vaginitis", "Vaginal candidosis", "MONILIAL VAGINITIS", "candidiasis vaginal", "vaginal candidiasis", "Vaginal candidiasis", "VAGINA, CANDIDIASIS", "VAGINAL CANDIDIASIS", "Vaginitis, Monilial", "Candidiasis of vagina", "Candida albicans vaginitis", "Monial infection of vagina", "Monilial infection of vagina", "vaginal candidiasis (diagnosis)", "Candidiasis of vagina (disorder)", "vaginitis due to Candida albicans", "vagina; candidiasis (manifestation)", "vaginitis due to Candida albicans (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Candidiasis of vagina", "shortest_name_length": 14}
{"curie": "MONDO:0000572", "names": ["recombinase activating gene 1 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "recombinase activating gene 1 deficiency", "shortest_name_length": 40}
{"curie": "MONDO:0019113", "names": ["Benign paroxysmal torticollis of infancy", "benign paroxysmal torticollis of infancy", "Benign paroxysmal torticollis of infancy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign paroxysmal torticollis of infancy", "shortest_name_length": 40}
{"curie": "UMLS:C0279069", "names": ["Recurrent LYG", "Recurrent Lymphomatoid Granulomatosis", "Relapsed Angiocentric Immunoproliferative Lesion", "Recurrent Angiocentric Immunoproliferative Lesion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Lymphomatoid Granulomatosis", "shortest_name_length": 13}
{"curie": "MONDO:0014520", "names": ["ODG4", "ovarian dysgenesis 4", "OVARIAN DYSGENESIS 4", "ovarian dysgenesis type 4", "46,XX ovarian dysgenesis-short stature syndrome", "46,XX ovarian dysgenesis, short stature syndrome", "46,XX ovarian dysgenesis, short stature syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XX ovarian dysgenesis-short stature syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C1387528", "names": ["Acute hemolytic anemia", "Acute haemolytic anaemia", "hemolytic; anemia, acute", "anemia; hemolytic, acute"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute haemolytic anaemia", "shortest_name_length": 22}
{"curie": "MONDO:0009733", "names": ["DMS", "NPHS4", "Mesangial sclerosis", "WT1 nephrotic syndrome", "nephrotic syndrome type 4", "nephrotic syndrome, type 4", "Diffuse Mesangial Sclerosis", "Diffuse mesangial sclerosis", "diffuse mesangial sclerosis", "Mesangial sclerosis, diffuse", "mesangial sclerosis, diffuse", "familial mesangial sclerosis", "Isolated diffuse mesangial sclerosis", "isolated diffuse mesangial sclerosis", "diffuse isolated mesangial sclerosis", "Diffuse isolated mesangial sclerosis", "Mesangial Sclerosis, Isolated Diffuse", "Diffuse mesangial sclerosis (disorder)", "Diffuse mesangial sclerosis glomerulopathy", "nephrotic syndrome caused by mutation in WT1", "congenital nephrotic syndrome - diffuse mesangial sclerosis", "Congenital Nephrotic Syndrome - Diffuse Mesangial Sclerosis", "Nephrotic syndrome, early onset with diffuse mesangial sclerosis", "nephrotic syndrome, early onset with diffuse mesangial sclerosis", "Nephrotic Syndrome, Early-Onset, With Diffuse Mesangial Sclerosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrotic syndrome, type 4", "shortest_name_length": 3}
{"curie": "UMLS:C4525620", "names": ["Ampulla of Vater Neuroendocrine Tumor by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ampulla of Vater Neuroendocrine Tumor by AJCC v8 Stage", "shortest_name_length": 54}
{"curie": "MONDO:0018014", "names": ["Transient neonatal MADD", "transient neonatal MADD", "transient neonatal MAD deficiency", "Transient neonatal MAD deficiency", "transient neonatal glutaric aciduria type 2", "transient neonatal glutaric acidemia type 2", "Transient neonatal glutaric acidemia type 2", "Transient neonatal glutaric aciduria type 2", "Transient neonatal glutaric acidaemia type 2", "Transient neonatal multiple acyl-CoA dehydrogenase deficiency", "transient neonatal multiple acyl-CoA dehydrogenase deficiency", "Transient neonatal multiple acyl-coenzyme A dehydrogenase deficiency", "Transient neonatal MAD (multiple acyl-coenzyme A dehydrogenase) deficiency", "Transient neonatal multiple acyl-coenzyme A dehydrogenase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transient neonatal multiple acyl-CoA dehydrogenase deficiency", "shortest_name_length": 23}
{"curie": "UMLS:C5237206", "names": ["Skin Verrucous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin Verrucous Carcinoma", "shortest_name_length": 24}
{"curie": "MONDO:0008690", "names": ["Xeroderma Pigmentosum, Autosomal Dominant, Mild", "XERODERMA PIGMENTOSUM, AUTOSOMAL DOMINANT, MILD", "xeroderma pigmentosum, autosomal dominant, mild"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "xeroderma pigmentosum, autosomal dominant, mild", "shortest_name_length": 47}
{"curie": "UMLS:C5243945", "names": ["Paradoxical psoriasis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paradoxical psoriasis", "shortest_name_length": 21}
{"curie": "UMLS:C5669725", "names": ["Extramedullary Disease in Multiple Myeloma Involving the Spleen", "Extramedullary Disease in Plasma Cell Myeloma Involving the Spleen"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extramedullary Disease in Plasma Cell Myeloma Involving the Spleen", "shortest_name_length": 63}
{"curie": "MONDO:0010844", "names": ["EDM2", "multiple epiphyseal dysplasia 2", "epiphyseal dysplasia multiple 2", "Multiple epiphyseal dysplasia, 2", "epiphyseal dysplasia, multiple, 2", "EPIPHYSEAL DYSPLASIA, MULTIPLE, 2", "Epiphyseal dysplasia, multiple, 2", "epiphyseal dysplasia, multiple, type 2", "COL9A2 multiple epiphyseal dysplasia (disease)", "multiple epiphyseal dysplasia (disease) caused by mutation in COL9A2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epiphyseal dysplasia, multiple, 2", "shortest_name_length": 4}
{"curie": "MONDO:0012817", "names": ["ES", "Ewing Tumor", "ewing tumor", "EWING TUMOR", "Ewing tumor", "Tumor, Ewing", "Ewings Tumor", "ewings tumor", "Ewing sarcoma", "ewing sarcoma", "Ewing's tumor", "EWING SARCOMA", "Ewing's Tumor", "sarcoma ewing", "Ewing Sarcoma", "ewings tumors", "ewing's tumor", "Ewings sarcoma", "Sarcoma, Ewing", "ewing's tumors", "Tumor, Ewing's", "Ewings Sarcoma", "sarcoma ewings", "SARCOMA, EWING", "ewings sarcoma", "localized PNET", "Ewing's tumour", "ewing's sarcoma", "PNET, localized", "localized pPNET", "sarcoma ewing's", "Ewing's Sarcoma", "Sarcoma, Ewings", "Ewing's sarcoma", "neuroepithelioma", "ewings's sarcoma", "Sarcoma, Ewing's", "sarcoma, Ewing's", "pPNET, localized", "Ewing's sarcoma NOS", "Localized Ewing Sarcoma", "localized Ewing sarcoma", "Ewing's tumor localized", "Localized Ewing's Tumor", "localized Ewing's tumor", "Ewing's tumour localised", "Ewing's sarcoma localized", "Ewing's sarcoma localised", "localized Ewing's sarcoma", "Localized Ewing's Sarcoma", "Ewing's Sarcoma, Localized", "Ewing's sarcoma, localized", "localized Ewing sarcoma/PNET", "neuroepithelioma, peripheral", "localized Ewing's sarcoma/PNET", "Ewing's family localized tumor", "PNET of Thoracopulmonary Region", "PNET of Thoracopulmonary region", "Ewing's sarcoma stage unspecified", "Localized Tumors of Ewing's Family", "localized peripheral neuroepithelioma", "localized tumors of the Ewing's family", "Localized tumors of the Ewing's family", "Localized Tumors of the Ewing's Family", "neuroepithelioma, localized, peripheral", "Ewing's sarcoma (morphologic abnormality)", "peripheral primitive neuroectodermal tumor", "localized peripheral neuroectodermal tumor", "peripheral neuroectodermal tumor, localized", "Ewings sarcoma-primitive neuroectodermal tumor", "localized primitive neuroectodermal tumor (PNET)", "primitive neuroectodermal tumor (PNET), localized", "localized peripheral primitive neuroectodermal tumor", "Localized Peripheral Primitive Neuroectodermal Tumor", "localized Ewing sarcoma/primitive neuroectodermal tumor", "localized Ewing's sarcoma/primitive neuroectodermal tumor", "Ewing's sarcoma/peripheral primitive neuroectodermal tumor", "localized Ewing sarcoma/peripheral primitive neuroectodermal tumor", "Localized Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor", "localized Ewing's sarcoma/peripheral primitive neuroectodermal tumor", "Localized Ewing's Sarcoma/Peripheral Primitive Neuroectodermal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ewing sarcoma", "shortest_name_length": 2}
{"curie": "UMLS:C1095924", "names": ["Fontanel Depressed", "Depressed Fontanel", "Fontanelle Depressed", "Fontanelle depressed", "depressed fontanelle", "fontanelle depressed", "depressed fontanelles"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fontanelle depressed", "shortest_name_length": 18}
{"curie": "UMLS:C0564750", "names": ["Peripheral arterial embolism", "embolism; arterial, peripheral", "Peripheral arterial embolism NOS", "Peripheral arterial embolism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peripheral arterial embolism", "shortest_name_length": 28}
{"curie": "MONDO:0004694", "names": ["Hepatopulmonary Syndrome", "hepatopulmonary syndrome", "Hepatopulmonary syndrome", "hepato pulmonary syndrome", "Hepato-Pulmonary Syndrome", "Syndrome, Hepatopulmonary", "Hepatopulmonary Syndromes", "Hepato Pulmonary Syndrome", "Syndrome, Hepato-Pulmonary", "Syndromes, Hepatopulmonary", "Hepato-Pulmonary Syndromes", "Syndromes, Hepato-Pulmonary", "Hepatopulmonary syndrome (disorder)", "hepatopulmonary syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatopulmonary syndrome", "shortest_name_length": 24}
{"curie": "UMLS:C5206582", "names": ["Advanced Colorectal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Colorectal Carcinoma", "shortest_name_length": 29}
{"curie": "UMLS:C4683497", "names": ["Refractory Lung Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Lung Carcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0003465", "names": ["fibrous synovial sarcoma", "Fibrous Synovial Sarcoma", "fibrous sarcoma of Synovium", "fibrous sarcoma of synovium", "Fibrous Sarcoma of Synovium", "fibrous sarcoma of the synovium", "Fibrous Sarcoma of the Synovium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibrous synovial sarcoma", "shortest_name_length": 24}
{"curie": "UMLS:C4055182", "names": ["Conventional Schwannoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conventional Schwannoma", "shortest_name_length": 23}
{"curie": "MONDO:0003655", "names": ["lymphoma brain", "Brain lymphoma", "brain lymphoma", "brain lymphomas", "cerebral lymphoma", "Cerebral Lymphoma", "Cerebral lymphoma", "primary brain lymphoma", "brain primary lymphoma", "brain lymphoma primary", "primary lymphoma, brain", "Primary Lymphoma, Brain", "primary cerebral lymphoma", "Primary cerebral lymphoma", "Primary Cerebral Lymphoma", "CEREBRAL LYMPHOMA PRIMARY", "PRIMARY LYMPHOMA OF BRAIN", "malignant lymphoma of brain", "primary Lymphoma of Cerebrum", "primary lymphoma of cerebrum", "Primary Lymphoma of Cerebrum", "Primary Lymphoma of the Cerebrum", "primary lymphoma of the cerebrum", "primary malignant lymphoma of brain", "Primary cerebral lymphoma (disorder)", "Primary cerebral lymphoma (diagnosis)", "malignant lymphoma of brain (diagnosis)", "malignant neoplasm lymphoma of brain primary", "primary malignant lymphoma of brain (diagnosis)", "neoplasm - brain cerebrum, malignant primary lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral lymphoma", "shortest_name_length": 14}
{"curie": "UMLS:C5205876", "names": ["CENTRAL NERVOUS SYSTEM RADIATION INJURY", "Central Nervous System Radiation Injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Radiation Injury", "shortest_name_length": 39}
{"curie": "MONDO:0016667", "names": ["Double heterozygotes sickling disorder", "sickle cell disease associated with an other hemoglobin anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sickle cell disease associated with an other hemoglobin anomaly", "shortest_name_length": 38}
{"curie": "MONDO:0004294", "names": ["gestational ovarian choriocarcinoma", "Ovarian Gestational Choriocarcinoma", "Gestational Ovarian Choriocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gestational ovarian choriocarcinoma", "shortest_name_length": 35}
{"curie": "MONDO:0011852", "names": ["NDNC8", "isolated toenail dystrophy", "toenail dystrophy, isolated", "TOENAIL DYSTROPHY, ISOLATED", "Toenail Dystrophy, Isolated", "COL7A1 inherited isolated nail anomaly", "nonsyndromic congenital nail disorder 8", "nail disorder, nonsyndromic congenital, 8", "NAIL DISORDER, NONSYNDROMIC CONGENITAL, 8", "nonsyndromic congenital nail disorder type 8", "nail disorder, nonsyndromic congenital, type 8", "inherited isolated nail anomaly caused by mutation in COL7A1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nonsyndromic congenital nail disorder 8", "shortest_name_length": 5}
{"curie": "MONDO:0010285", "names": ["MRXSAB", "Mental retardation X-linked, Abidi type", "Mental Retardation, X-Linked, Abidi Type", "ABIDI X-LINKED MENTAL RETARDATION SYNDROME", "ABIDI X-linked mental retardation syndrome", "Abidi X-linked mental retardation syndrome", "intellectual disability X-linked Abidi type", "X-linked intellectual disability, Abidi type", "ABIDI X-linked intellectual disability syndrome", "syndromic X-linked mental retardation Abidi type", "mental retardation, X-linked syndromic, Abidi type", "mental retardation, X-linked, syndromic, Abidi type", "MENTAL RETARDATION, X-LINKED, SYNDROMIC, ABIDI TYPE", "syndromic X-linked intellectual disability Abidi type", "intellectual disability, X-linked syndromic, Abidi type", "intellectual disability, X-linked, syndromic, Abidi type", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, ABIDI TYPE", "Short stature, small head circumference, sloping forehead, hearing loss, cupped ears and small testes", "short stature, small head circumference, sloping forehead, hearing loss, cupped ears and small testes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic X-linked intellectual disability Abidi type", "shortest_name_length": 6}
{"curie": "UMLS:C1334608", "names": ["Malignant Ovarian Luteinized Thecoma", "Malignant Luteinized Thecoma of Ovary", "Malignant Luteinized Thecoma of the Ovary", "Malignant Ovarian Luteinized Thecal Cell Tumor", "Malignant Luteinized Thecal Cell Tumor of Ovary", "Malignant Ovarian Luteinized Thecal Cell Neoplasm", "Malignant Luteinized Thecal Cell Neoplasm of Ovary", "Malignant Luteinized Thecal Cell Tumor of the Ovary", "Malignant Luteinized Thecal Cell Neoplasm of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Ovarian Luteinized Thecoma", "shortest_name_length": 36}
{"curie": "MONDO:0010914", "names": ["CPT 2 deficiency, hepatic", "Cpt2 deficiency, infantile", "CPT II DEFICIENCY, HEPATIC", "CPT2 DEFICIENCY, INFANTILE", "CPT II Deficiency, Hepatic", "CPT2 Deficiency, Infantile", "CPT2, severe infantile form", "CPT II deficiency, infantile", "CPTII, severe infantile form", "CPT2, hepatocardiomuscular form", "CPTII, hepatocardiomuscular form", "Carnitine Palmitoyltransferase 2 deficiency, infantile", "CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE", "CARNITINE PALMITOYLTRANSFERASE II deficiency, infantile", "Carnitine Palmitoyltransferase II Deficiency, Infantile", "Carnitine Palmitoyltransferase 2 deficiency, hepatocardiomuscular", "CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, HEPATOCARDIOMUSCULAR", "Carnitine Palmitoyltransferase II Deficiency, Hepatocardiomuscular", "carnitine palmitoyl transferase II deficiency, severe infantile form", "Carnitine palmitoyl transferase II deficiency, severe infantile form", "Carnitine palmitoyl transferase II deficiency, hepatocardiomuscular form", "Carnitine palmitoyl transferase deficiency type 2, severe infantile form", "Carnitine Palmitoyltransferase 2 deficiency with hypoketotic hypoglycemia", "Carnitine Palmitoyltransferase II Deficiency with Hypoketotic Hypoglycemia", "CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY WITH HYPOKETOTIC HYPOGLYCEMIA", "Carnitine palmitoyl transferase deficiency type 2, hepatocardiomuscular form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carnitine palmitoyl transferase II deficiency, severe infantile form", "shortest_name_length": 25}
{"curie": "MONDO:0018184", "names": ["Gastric linitis plastica", "gastric linitis plastica", "Linitis plastica of stomach", "Borrmann gastric cancer type 4", "Linitis plastica of the stomach", "linitis plastica of the stomach", "Linitis plastica of stomach (disorder)", "Linitis plastica of stomach (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric linitis plastica", "shortest_name_length": 24}
{"curie": "UMLS:C3898748", "names": ["Insufficient Milk Syndrome", "Insufficient Breast Milk Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Insufficient Breast Milk Syndrome", "shortest_name_length": 26}
{"curie": "MONDO:0009845", "names": ["Cousin syndrome", "COUSIN SYNDROME", "Cousin Syndrome", "COUSIN syndrome", "PELVISCAPULAR DYSPLASIA", "Pelviscapular dysplasia", "pelviscapular dysplasia", "Pelvic shoulder dysplasia", "Pelviscapular dysplasia syndrome", "Familial pelvis-scapular dysplasia", "familial pelvis-scapular dysplasia", "Pelviscapular dysplasia syndrome (disorder)", "craniofacial dysmorphism, hypoplasia of scapula and pelvis and short stature", "CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORT STATURE", "Craniofacial Dysmorphism, Hypoplasia of Scapula and Pelvis, and Short Stature", "craniofacial Dysmorphism, hypoplasia of scapula and pelvis, and short stature"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pelviscapular dysplasia", "shortest_name_length": 15}
{"curie": "UMLS:C0392190", "names": ["STOMATITIS RADIATION", "Stomatitis radiation", "Radiation stomatitis", "Radiation-induced mucositis", "Radiation-Induced Stomatitis", "Ulcerative mucositis due to radiation", "Mucositis following radiation therapy", "Mucositis following radiation therapy (disorder)", "Oral mucositis due to exposure to ionizing radiation", "Radiation-induced mucositis of oral mucous membranes", "Oral mucositis due to exposure to ionising radiation", "Radiation-induced mucositis of oral mucous membranes (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mucositis following radiation therapy", "shortest_name_length": 20}
{"curie": "UMLS:C2981160", "names": ["Stage 0 Esophageal Cancer", "Esophageal Cancer Stage 0 AJCC v6", "Stage 0 Esophageal Cancer AJCC v6", "Esophagus Carcinoma in situ AJCC v6", "Severe Esophageal Dysplasia AJCC v6", "Stage 0 Esophagus Carcinoma AJCC v6", "Stage 0 Esophageal Carcinoma AJCC v6", "Esophageal Carcinoma in situ AJCC v6", "Esophageal Carcinoma Stage 0 AJCC v6", "Carcinoma in situ of Esophagus AJCC v6", "Stage 0 Carcinoma of Esophagus AJCC v6", "Oesophageal Carcinoma NOS Stage 0 AJCC v6", "Stage 0 Carcinoma of the Esophagus AJCC v6", "Carcinoma in situ of the Esophagus AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Esophageal Cancer AJCC v6", "shortest_name_length": 25}
{"curie": "UMLS:C3251817", "names": ["Warty carcinoma", "Warty Carcinoma", "Condylomatous carcinoma", "Warty (condylomatous) carcinoma", "Warty (condylomatous) carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Condylomatous carcinoma", "shortest_name_length": 15}
{"curie": "UMLS:C0702120", "names": ["Spongiosis", "spongiosis", "Intraepidermal edema", "intraepidermal edema", "Edema, intraepidermal", "Intraepidermal oedema", "Spongiosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spongiosis", "shortest_name_length": 10}
{"curie": "MONDO:0011587", "names": ["CCSSO", "CTRCT25", "CATARACT 25", "cataract 25", "cataract type 25", "Early-onset sutural cataract", "central saccular cataract with sutural opacities", "CATARACT, CENTRAL SACCULAR, WITH SUTURAL OPACITIES", "Cataract, Central Saccular, With Sutural Opacities", "central pouch-like cataract with sutural opacities", "cataract, central saccular, with sutural opacities", "Early-onset cataract with Y-shaped suture opacities", "early-onset cataract with Y-shaped suture opacities", "cataract, central pouch-like, with sutural opacities", "Cataract, Central Pouch-Like, With Sutural Opacities", "CATARACT, CENTRAL POUCH-LIKE, WITH SUTURAL OPACITIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 25", "shortest_name_length": 5}
{"curie": "MONDO:0000498", "names": ["AAION", "arteritic aion", "Arteritic anterior ischemic optic neuropathy", "ischemic optic neuropathy arteritic anterior", "arteritic anterior ischemic optic neuropathy", "Arteritic anterior ischaemic optic neuropathy", "AAION - arteritic anterior ischemic optic neuropathy", "AAION - arteritic anterior ischaemic optic neuropathy", "Arteritic anterior ischemic optic neuropathy (disorder)", "Arteritic anterior ischemic optic neuropathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arteritic anterior ischemic optic neuropathy", "shortest_name_length": 5}
{"curie": "UMLS:C5238360", "names": ["Metastatic Primary Peritoneal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Primary Peritoneal Carcinoma", "shortest_name_length": 39}
{"curie": "MONDO:0004674", "names": ["chorioretinitis", "CHORIORETINITIS", "Chorioretinitis", "retinochoroiditis", "Retinochoroiditis", "Chorioretinitides", "CHORIODORETINITIS", "Chorioretinitis NOS", "Chorioretinitis, NOS", "Retinochoroiditis NOS", "chorioretinitis (disease)", "Choroiditis and retinitis", "chorioretinal inflammation", "Chorioretinitis (disorder)", "Chorioretinal inflammation", "chorioretinitis (diagnosis)", "Chorioretinitis, unspecified", "Inflammation of choroid and retina", "chorioretinitis (physical finding)", "chorioretinal inflammation (diagnosis)", "Unspecified chorioretinal inflammation", "Chorioretinal inflammation, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chorioretinitis", "shortest_name_length": 15}
{"curie": "UMLS:C0235620", "names": ["urinary tract bleeding", "Bleeding urinary tract", "BLEEDING URINARY TRACT", "URINARY TRACT BLEEDING", "bleeding urinary tract", "Urinary tract bleeding", "bleeding tract urinary", "HEMORRHAGE URINARY TRACT", "Urinary Tract Hemorrhage", "Hemorrhage urinary tract", "Haemorrhage urinary tract", "Urinary System Hemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemorrhage urinary tract", "shortest_name_length": 22}
{"curie": "UMLS:C0270897", "names": ["Erb", "Erb Palsy", "erb palsy", "ERB PALSY", "Erbs Palsy", "palsy; Erb", "Erb; palsy", "erbs palsy", "erb's palsy", "Erb's Palsy", "Erb's palsy", "Palsy, Erb's", "Erb's Palsies", "Erb Paralyses", "erb paralysis", "Erb Paralysis", "Paralysis, Erb", "paralysis; Erb", "Paralyses, Erb", "Erb; paralysis", "Palsies, Erb's", "erb's paralysis", "Erb's paralysis", "Erb-Duchenne Palsy", "Erb-Duchenne Paralyses", "Erb Duchenne paralysis", "Erb Duchenne Paralysis", "erb-duchenne paralysis", "Erb-Duchenne Paralysis", "Erb-Duchenne paralysis", "Paralysis, Erb-Duchenne", "Paralyses, Erb-Duchenne", "Erb-Duchenne paralysis (disorder)", "Erb-Duchenne paralysis (diagnosis)", "Erb Duchenne brachial plexus injury", "Erb-Duchenne brachial plexus injury", "Upper brachial plexus paralysis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Erb-Duchenne Paralysis", "shortest_name_length": 3}
{"curie": "MONDO:0013721", "names": ["C4AD", "C4A deficiency", "C4A DEFICIENCY", "C4a deficiency", "Decreased serum complement C4a", "complement component 4A deficiency", "complement component 4a deficiency", "Complement component 4A deficiency", "COMPLEMENT COMPONENT 4A DEFICIENCY", "Complement Component 4a Deficiency", "C4A classic complement early component deficiency", "Decreased circulating complement C4a concentration", "classic complement early component deficiency caused by mutation in C4A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complement component 4a deficiency", "shortest_name_length": 4}
{"curie": "UMLS:C0268386", "names": ["Rakavina type amyloidosis", "type II neuropathic amyloidosis", "Swiss type amyloid polyneuropathy", "Swiss Type Amyloid Polyneuropathy", "German type amyloid polyneuropathy", "Amyloidosis, Indiana-Maryland type", "Amyloid Polyneuropathy, Swiss Type", "Familial amyloid polyneuropathy type II", "Type II Familial Amyloid Polyneuropathy", "Familial Amyloid Polyneuropathy, Type II", "Familial amyloid polyneuropathy, type II", "Hereditary neuropathic amyloidosis, type II", "type II neuropathic amyloidosis (diagnosis)", "Indiana-Maryland type amyloid polyneuropathy", "Familial amyloid polyneuropathy, 84 Ser-for-Ile", "Familial amyloid polyneuropathy, type II (disorder)", "Familial amyloid polyneuropathy, Indiana-Swiss type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Amyloid Polyneuropathy, Swiss Type", "shortest_name_length": 25}
{"curie": "MONDO:0013581", "names": ["MRD2", "autosomal dominant mental retardation 2", "mental retardation, autosomal dominant 2", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 2", "autosomal dominant intellectual disability 2", "mental retardation, autosomal dominant type 2", "intellectual disability, autosomal dominant 2", "intellectual disability, autosomal dominant type 2", "autosomal dominant intellectual developmental disorder 2", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 2", "autosomal dominant non-syndromic intellectual disability 2", "DOCK8 autosomal dominant non-syndromic intellectual disability", "autosomal dominant non-syndromic intellectual disability caused by mutation in DOCK8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 2", "shortest_name_length": 4}
{"curie": "UMLS:C4528742", "names": ["Stage II Low-CSD Melanoma AJCC v7", "Stage II Superficial Spreading Melanoma", "Stage II Superficial Spreading Melanoma AJCC v6 and v7", "Stage II Superficial Spreading Cutaneous (Skin) Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Low-CSD Melanoma AJCC v7", "shortest_name_length": 33}
{"curie": "UMLS:C5238465", "names": ["Metastatic Midgut Neuroendocrine Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Midgut Neuroendocrine Tumor", "shortest_name_length": 38}
{"curie": "MONDO:0017355", "names": ["disorder of proline metabolism", "inborn disorder of proline metabolism", "inborn error of proline metabolic process", "inborn proline metabolic process disorder", "rare inborn error of proline metabolic process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of proline metabolism", "shortest_name_length": 30}
{"curie": "MONDO:0003543", "names": ["trigeminal disorder", "disorder trigeminal", "Trigeminal disorders", "trigeminal neuropathy", "Trigeminal Neuropathy", "neuropathy trigeminal", "Trigeminal neuropathy", "Neuropathy, Trigeminal", "Trigeminal Neuropathies", "Trigeminal Nerve Disease", "Cranial Nerve V Diseases", "Neuropathies, Trigeminal", "trigeminal nerve disease", "Trigeminal nerve disorder", "disorder trigeminal nerve", "trigeminal nerve disorder", "Trigeminal Nerve Diseases", "Trigeminal Nerve Disorder", "Trigeminal Nerve Disorders", "Trigeminal nerve disorders", "Trigeminal nerve--Diseases", "disease of trigeminal nerve", "Disorder of cranial nerve 5", "Fifth cranial nerve disorder", "Disorder of trigeminal nerve", "Fifth Cranial Nerve Diseases", "disorder of trigeminal nerve", "Disorders of the fifth nerve", "disorders of the fifth nerve", "Disorders of trigeminal nerve", "Trigeminal nerve disorder NOS", "Trigeminal nerve disorder, NOS", "trigeminal neuropathy (diagnosis)", "disorders of the vth cranial nerve", "Disorders of the Vth cranial nerve", "Disorder of the fifth cranial nerve", "disorder of the fifth cranial nerve", "trigeminal nerve disease or disorder", "Trigeminal nerve disease or syndrome", "Trigeminal nerve disorder (disorder)", "Trigeminal nerve disorder, unspecified", "Fifth cranial nerve disease or syndrome", "disease (or disorder); trigeminal nerve", "disease or disorder of trigeminal nerve", "disorder of trigeminal nerve (diagnosis)", "Disorder of the fifth cranial nerve, NOS", "Disorder of trigeminal nerve, unspecified", "Other specified trigeminal nerve disorders", "disease (or disorder); cranial nerve, fifth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trigeminal nerve disorder", "shortest_name_length": 19}
{"curie": "MONDO:0005006", "names": ["CCSK", "renal clear cell sarcoma", "Renal Clear Cell Sarcoma", "renal Clear cell sarcoma", "clear cell sarcoma kidney", "Kidney Clear Cell Sarcoma", "kidney clear cell sarcoma", "kidney; clear cell sarcoma", "sarcoma; clear cell, kidney", "clear cell sarcoma - kidney", "clear cell; sarcoma, kidney", "kidney; sarcoma, clear cell", "Clear cell sarcoma - kidney", "Clear Cell Sarcoma of Kidney", "Clear cell sarcoma of kidney", "clear cell sarcoma of kidney", "Clear cell sarcoma of the kidney", "Clear Cell Sarcoma of the Kidney", "clear cell sarcoma of the kidney", "childhood renal clear cell sarcoma", "Pediatric Renal Clear Cell Sarcoma", "pediatric renal clear cell sarcoma", "Childhood Renal Clear Cell Sarcoma", "Childhood Kidney Clear Cell Sarcoma", "CCSK - clear cell sarcoma of kidney", "childhood kidney clear cell sarcoma", "pediatric kidney clear cell sarcoma", "Pediatric Kidney Clear Cell Sarcoma", "Clear cell sarcoma of kidney (disorder)", "Clear cell sarcoma of the kidney (CCSK)", "clear cell sarcoma of kidney (diagnosis)", "Childhood Clear Cell Sarcoma of the Kidney", "childhood clear cell sarcoma of the kidney", "Clear cell sarcoma of kidney (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "clear cell sarcoma of kidney", "shortest_name_length": 4}
{"curie": "UMLS:C0854811", "names": ["Refractory Lymphocyte Depleted Hodgkin Lymphoma", "Refractory Lymphocyte Depleted Hodgkin's Disease", "Refractory Hodgkin's Disease Lymphocyte Depleted", "Refractory Lymphocyte Depleted Hodgkin's Lymphoma", "Refractory Hodgkin's Lymphoma Lymphocyte Depleted", "Hodgkin's disease lymphocyte depletion type refractory", "Refractory Hodgkin's Lymphoma Lymphocyte Depletion Type", "Refractory Lymphocyte-Depleted Classic Hodgkin Lymphoma", "Refractory Lymphocyte-Depleted Classical Hodgkin Lymphoma", "Refractory Lymphocyte Depleted Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's disease lymphocyte depletion type refractory", "shortest_name_length": 47}
{"curie": "MONDO:0001607", "names": ["hairy cell leukemia of intrapelvic site", "hairy cell leukemia of intrapelvic site (diagnosis)", "intrapelvic lymph node leukemic reticuloendotheliosis", "Leukemic reticuloendotheliosis, intrapelvic lymph nodes", "leukemic reticuloendotheliosis of intrapelvic lymph nodes", "Leukemic reticuloendotheliosis of intrapelvic lymph nodes", "Leukaemic reticuloendotheliosis of intrapelvic lymph nodes", "leukemic reticuloendotheliosis involving intrapelvic lymph nodes", "Leukemic reticuloendotheliosis involving intrapelvic lymph nodes", "Leukaemic reticuloendotheliosis involving intrapelvic lymph nodes", "Leukemic reticuloendotheliosis of intrapelvic lymph nodes (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intrapelvic lymph node leukemic reticuloendotheliosis", "shortest_name_length": 39}
{"curie": "UMLS:C0016510", "names": ["Foot Disease", "disease foot", "foot disease", "Foot Diseases", "diseases foot", "foot diseases", "Foot--Diseases", "disease of foot", "Disorder of foot", "Disorder of foot (disorder)", "Disorder of foot (diagnosis)", "disorder of lower extremity foot"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Foot Diseases", "shortest_name_length": 12}
{"curie": "MONDO:0015566", "names": ["Del(2)(q24)", "2q24 deletion", "Monosomy 2q24", "Deletion 2q24", "monosomy 2q24", "deletion 2q24", "Chromosome 2, monosomy 2q24", "2q24 microdeletion syndrome", "2q24 microdeletion syndrome (disorder)", "chromosome 2q24 microdeletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "2q24 microdeletion syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0030034", "names": ["EPM11", "EPILEPSY, PROGRESSIVE MYOCLONIC, 11", "epilepsy, progressive myoclonic, 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, progressive myoclonic, 11", "shortest_name_length": 5}
{"curie": "MONDO:0007315", "names": ["CRBM", "Crbm", "cherubism", "CHERUBISM", "Cherubism", "cherubism of jaw", "jaw; fibrous dysplasia", "dysplasia; fibrous, jaw", "fibrous; dysplasia, jaw", "jaw; dysplasia, fibrous", "Fibrous dysplasia of jaw", "fibrous dysplasia of jaw", "Fibrous dysplasia of jaws", "cherubism of jaw (diagnosis)", "dysplasia familial fibrous jaw", "Familial fibrous dysplasia of jaw", "Familial Fibrous Dysplasia of Jaw", "Fibrous dysplasia of jaw (disorder)", "fibrous dysplasia of jaw (diagnosis)", "Familial Fibrous Dysplasia of the Jaws", "familial fibrous dysplasia of the jaws", "Familial Benign Giant-Cell Tumor of the Jaw", "Familial Multilocular Cystic Disease of the Jaws", "Familial multilocular cystic disease of the jaws", "familial multilocular cystic disease of the jaws"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cherubism", "shortest_name_length": 4}
{"curie": "MONDO:0002837", "names": ["Transitional Spindle Cell Carcinoma", "transitional spindle cell carcinoma", "Sarcomatoid Transitional Cell Carcinoma", "sarcomatoid transitional cell carcinoma", "transitional cell carcinoma, sarcomatoid", "Transitional cell carcinoma, sarcomatoid", "Transitional Cell Spindle Cell Carcinoma", "transitional cell spindle cell carcinoma", "spindle cell transitional cell carcinoma", "Transitional cell carcinoma, spindle cell", "transitional cell carcinoma, spindle cell", "Transitional cell carcinoma - spindle cell", "Transitional cell carcinoma, spindle cell type", "spindle cell transitional cell carcinoma (diagnosis)", "Transitional cell carcinoma, spindle cell (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sarcomatoid transitional cell carcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C3897939", "names": ["Anti-Mullerian Hormone Deficiency", "Persistent Mullerian Duct Syndrome Type 1", "Persistent Mullerian Duct Syndrome Type I", "Persistent Müllerian Duct Syndrome Type 1", "PERSISTENT MULLERIAN DUCT SYNDROME, TYPE I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PERSISTENT MULLERIAN DUCT SYNDROME, TYPE I", "shortest_name_length": 33}
{"curie": "MONDO:0018133", "names": ["atypical Chédiak-Higashi syndrome", "Atypical Chédiak-Higashi syndrome", "atypical Chediak-Higashi syndrome", "attenuated Chediak-Higashi syndrome", "Attenuated Chédiak-Higashi syndrome", "attenuated Chédiak-Higashi syndrome", "Attenuated Chédiak-Higashi syndrome (disorder)", "attenuated Chediak-Higashi syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "attenuated Chédiak-Higashi syndrome", "shortest_name_length": 33}
{"curie": "MONDO:0020197", "names": ["EEC syndrome and related syndrome", "ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome and related disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "EEC syndrome and related syndrome", "shortest_name_length": 33}
{"curie": "UMLS:C0221165", "names": ["diplegia", "DIPLEGIA", "Diplegia", "Diplegia, NOS", "Bilateral paralysis", "Diplegia (disorder)", "Bilateral paralysis, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diplegia", "shortest_name_length": 8}
{"curie": "MONDO:0014868", "names": ["DEE38", "EIEE38", "GPIBD23", "early infantile epileptic encephalopathy 38", "ARV1 early infantile epileptic encephalopathy", "developmental and epileptic encephalopathy 38", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 38", "epileptic encephalopathy, early infantile, 38", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 38", "developmental and epileptic encephalopathy, 38", "epileptic encephalopathy, early infantile, type 38", "GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 23", "epileptic encephalopathy, early infantile, 38; EIEE38", "early infantile epileptic encephalopathy caused by mutation in ARV1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 38", "shortest_name_length": 5}
{"curie": "MONDO:0010670", "names": ["mental retardation with spastic paraplegia", "MENTAL RETARDATION WITH SPASTIC PARAPLEGIA", "Mental Retardation with Spastic Paraplegia", "intellectual disability with spastic paraplegia", "X-linked intellectual disability-spastic quadriparesis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability-spastic quadriparesis syndrome", "shortest_name_length": 42}
{"curie": "MONDO:0022978", "names": ["diaphragmatic hernia upper limb defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diaphragmatic hernia upper limb defects", "shortest_name_length": 39}
{"curie": "UMLS:C0854775", "names": ["stage IV pancreas cancer", "pancreas cancer, stage IV", "Pancreatic Cancer Stage IV", "stage IV pancreatic cancer", "pancreatic cancer, stage IV", "Pancreatic carcinoma stage IV", "Stage IV Pancreatic Carcinoma", "Stage IV Carcinoma of Pancreas", "Metastatic Pancreatic Carcinoma", "Pancreatic carcinoma metastatic", "Stage IV Carcinoma of the Pancreas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stage IV pancreatic cancer", "shortest_name_length": 24}
{"curie": "MONDO:0008938", "names": ["EOCA", "EOCARR", "Harding ataxia", "Charlevoix ataxia", "Ataxia, harding type", "ataxia, harding type", "Cerebellar ataxia early onset with retained tendon reflex", "cerebellar ataxia early onset with retained tendon reflex", "Early onset cerebellar ataxia with retained tendon reflexes", "Early-onset cerebellar ataxia with retained tendon reflexes", "early-onset cerebellar ataxia with retained tendon reflexes", "CEREBELLAR ATAXIA, EARLY-ONSET, WITH RETAINED TENDON REFLEXES", "Cerebellar Ataxia, Early-Onset, with Retained Tendon Reflexes", "cerebellar ataxia, early-onset, with retained tendon reflexes", "EOCA - Early onset cerebellar ataxia with retained tendon reflexes", "Early onset cerebellar ataxia with retained tendon reflexes (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early-onset cerebellar ataxia with retained tendon reflexes", "shortest_name_length": 4}
{"curie": "UMLS:C0751037", "names": ["Cockayne Syndrome Type 3", "Cockayne syndrome type 3", "Type C Cockayne Syndrome", "Cockayne syndrome type C", "Cockayne Syndrome Type C", "Cockayne Syndrome, Type C", "Group C Cockayne Syndrome", "Cockayne Syndrome, Group C", "Cockayne syndrome type III", "Type III Cockayne Syndrome", "Cockayne Syndrome, Type III", "Cockayne syndrome type 3 (disorder)", "Cockayne syndrome type C (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cockayne Syndrome, Type III", "shortest_name_length": 24}
{"curie": "UMLS:C4688649", "names": ["Lugano Classification Advanced Stage Adult Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Advanced Stage Adult Lymphoma AJCC v8", "shortest_name_length": 59}
{"curie": "MONDO:0013448", "names": ["GEFSP8", "GEFS+8", "GEFS+, TYPE 8", "Gefs+, type 8", "generalized epilepsy with febrile seizures plus 8", "generalised epilepsy with febrile seizures plus 8", "generalised epilepsy with febrile seizures plus type 8", "generalized epilepsy with febrile seizures plus type 8", "generalized epilepsy with febrile seizures plus, type 8", "GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "generalized epilepsy with febrile seizures plus, type 8", "shortest_name_length": 6}
{"curie": "MONDO:0044342", "names": ["Disc degeneration;thoracic", "thoracic Disc Degeneration", "Thoracic Disc Degeneration", "Thoracic disc degeneration", "thoracic disc degeneration", "Thoracic Disc Degenerative Disease", "thoracic Disc degenerative disease", "Thoracic Disc Degenerative Disorder", "thoracic disc degenerative disorder", "thoracic Disc degenerative disorder", "degeneration; intervertebral disc, thoracic", "degeneration of thoracic intervertebral disc", "Degeneration of thoracic intervertebral disc", "Degeneration of thoracic intervertebral disc (disorder)", "degeneration of thoracic intervertebral disc (diagnosis)", "thoracic region of vertebral column intervertebral disc degenerative disorder", "intervertebral disc degenerative disorder of thoracic region of vertebral column"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thoracic disc degenerative disorder", "shortest_name_length": 26}
{"curie": "MONDO:0006295", "names": ["Urologic Cancer", "Urologic Cancers", "Cancer, Urologic", "Cancers, Urologic", "Urological Cancer", "urological cancer", "Cancer, Urological", "Urological Cancers", "urological cancers", "Cancers, Urological", "renal system cancer", "cancer urinary tract", "Urinary Tract Cancer", "urinary tract cancer", "Urinary Tract Cancers", "kidney/urinary cancer", "urinary system cancer", "Cancer, Urinary Tract", "cancer system urinary", "Cancers, Urinary Tract", "cancer of renal system", "Urinary organs--Cancer", "Cancer of urinary organ", "Cancer of Urinary Tract", "Cancer of urinary organs", "Neoplasm malig;urological", "Cancer of the Urinary Tract", "Urothelial/bladder cancer, NOS", "malignant renal system neoplasm", "Malignant tumor of urinary tract", "Malignant Urinary Tract Neoplasm", "malignant urinary tract neoplasm", "Malignant urinary tract neoplasm", "Malignant Urinary System Neoplasm", "malignant neoplasm urinary system", "Malignant tumour of urinary tract", "malignant urinary system neoplasm", "malignant neoplasm of renal system", "Malignant neoplasm of urinary organ", "malignant neoplasm of urinary organs", "Malignant neoplasms of urinary tract", "Malignant urinary tract neoplasm NOS", "Urothelial tract/bladder cancer, NOS", "malignant neoplasm of urinary system", "Malignant tumor of urinary tract proper", "Malignant tumour of urinary tract proper", "Malignant neoplasm of urinary system NOS", "Malignant neoplasm of urinary system, NOS", "urinary neoplasm malignant of tract proper", "malignant neoplasm of urinary tract proper", "malignant neosplasm of the urological system", "Malignant neoplasms of urinary tract (C64-C68)", "Malignant neoplasm of urinary organ (disorder)", "malignant neoplasm of urinary system (diagnosis)", "malignant neoplasm of urinary organs (diagnosis)", "Malignant neoplasm of urinary organ, unspecified", "Malignant tumor of urinary tract proper (disorder)", "Malignant neoplasm of urinary organ, site unspecified", "malignant neoplasm of urinary tract proper (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant urinary system neoplasm", "shortest_name_length": 15}
{"curie": "MONDO:0008425", "names": ["Shprintzen omphalocele syndrome", "SHPRINTZEN OMPHALOCELE SYNDROME", "Shprintzen Goldberg omphalocele syndrome", "Shprintzen-Goldberg omphalocele syndrome", "Omphalocele syndrome Shprintzen Goldberg type", "Pharynx and larynx hypoplasia with omphalocele", "PHARYNX AND LARYNX HYPOPLASIA WITH OMPHALOCELE", "omphalocele syndrome, Shprintzen-Goldberg type", "Omphalocele syndrome, Shprintzen-Goldberg type", "pharynx and larynx hypoplasia with omphalocele", "Shprintzen Goldberg omphalocele syndrome (disorder)", "Laryngeal and pharyngeal hypoplasia with omphalocele", "laryngeal and pharyngeal hypoplasia with omphalocele", "OMPHALOCELE WITH HYPOPLASIA OF PHARYNX AND LARYNX, LEARNING DISABILITY, DYSMORPHIC FACIES, AND SCOLIOSIS", "omphalocele with hypoplasia of pharynx and larynx, learning disability, dysmorphic facies, and scoliosis", "omphalocele, laryngeal and pharyngeal hypoplasia, learning disabilities, dysmorphic facies and spinal anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "omphalocele syndrome, Shprintzen-Goldberg type", "shortest_name_length": 31}
{"curie": "UMLS:C4329628", "names": ["Central Nervous System Desmoid Fibromatosis", "Central Nervous System Desmoid-Type Fibromatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Desmoid Fibromatosis", "shortest_name_length": 43}
{"curie": "MONDO:0012631", "names": ["AD14", "ALZHEIMER DISEASE 14", "Alzheimer disease-14", "Alzheimer disease 14", "Alzheimer Disease 14", "Alzheimer's disease 14", "Alzheimer's disease type 14", "Alzheimer's disease 14, late onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alzheimer disease 14", "shortest_name_length": 4}
{"curie": "MONDO:0014236", "names": ["EDSMC2", "Ehlers-Danlos syndrome kyphoscoliotic type 2", "Ehlers-Danlos syndrome musculocontractural type 2", "Ehlers-Danlos syndrome, musculocontractural type 2", "EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2", "Ehlers-Danlos syndrome, musculocontractural type, 2", "DSE Ehlers-Danlos syndrome, musculocontractural type", "Ehlers-Danlos syndrome, musculocontractural type caused by mutation in DSE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ehlers-Danlos syndrome, musculocontractural type 2", "shortest_name_length": 6}
{"curie": "MONDO:0010551", "names": ["CMTX3", "CMT3X", "CMTX 3", "X-linked Charcot-Marie-Tooth disease type 3", "Charcot-Marie-Tooth disease X-linked, 3 (CMTX3)", "Charcot Marie Tooth disease X-linked recessive 3", "Charcot-Marie-Tooth disease X-linked recessive 3", "Charcot-Marie-Tooth disease, X-linked recessive, 3", "CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 3", "Charcot-Marie-Tooth neuropathy X-linked recessive 3", "Charcot-Marie-Tooth disease X-linked recessive type 3", "Charcot-Marie-Tooth Neuropathy, X-Linked Recessive, 3", "CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED RECESSIVE, 3", "Charcot-Marie-Tooth neuropathy, X-linked recessive, 3", "X-linked Charcot-Marie-Tooth disease type 3 (disorder)", "Charcot-Marie-Tooth disease X-linked, 3 (CMTX3) (diagnosis)", "CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 3 (disorder)", "Charcot-Marie-Tooth neuropathy, X-linked recessive, 3, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease X-linked recessive 3", "shortest_name_length": 5}
{"curie": "MONDO:0009128", "names": ["MOLLICA SYNDROME", "Mollica syndrome", "Mollica Pavone Antener syndrome", "Mollica-Pavone-Anterer syndrome", "dwarfism, mental retardation, and eye abnormality", "Dwarfism, mental retardation, and eye abnormality", "DWARFISM, MENTAL RETARDATION, AND EYE ABNORMALITY", "dwarfism, intellectual disability, and eye abnormality", "Short stature, mental retardation and ocular alterations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dwarfism, intellectual disability, and eye abnormality", "shortest_name_length": 16}
{"curie": "UMLS:C5204784", "names": ["Platinum Sensitive Ovarian Cancer", "Platinum-Sensitive Ovarian Cancer", "Platinum-Sensitive Ovarian Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Platinum-Sensitive Ovarian Carcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C0853846", "names": ["Deliberate poisoning", "Poisoning deliberate", "intentional poisoning", "Intentional poisoning", "Intentional poisoning (disorder)", "intentional poisoning (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intentional poisoning", "shortest_name_length": 20}
{"curie": "UMLS:C3888469", "names": ["Medical device site erythema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Medical device site erythema", "shortest_name_length": 28}
{"curie": "MONDO:0002802", "names": ["functional colonic disease", "Functional Colonic Disease", "colon; disease, functional", "Functional Colonic Diseases", "Colonic Disease, Functional", "Disease, Functional Colonic", "Diseases, Functional Colonic", "Colonic Diseases, Functional", "disease (or disorder); colon, functional"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "functional colonic disease", "shortest_name_length": 26}
{"curie": "MONDO:0018845", "names": ["focal myositis", "focal nodular myositis", "Focal nodular myositis", "Localized nodular myositis", "Localised nodular myositis", "Focal nodular myositis (disorder)", "inflammatory pseudotumor of skeletal muscle"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal myositis", "shortest_name_length": 14}
{"curie": "MONDO:0002034", "names": ["cecal lymphoma", "Cecum Lymphoma", "Cecal Lymphoma", "cecum lymphoma", "caecum lymphoma", "Lymphoma of Cecum", "lymphoma of cecum", "lymphoma of caecum", "lymphoma of the cecum", "Lymphoma of the Cecum", "Primary Cecum Lymphoma", "primary cecum lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cecum lymphoma", "shortest_name_length": 14}
{"curie": "MONDO:0003283", "names": ["epididymis tumor", "Epididymal Neoplasm", "tumor of epididymis", "epididymal neoplasm", "Epididymal neoplasm", "Tumor of epididymis", "epididymis neoplasm", "Tumour of epididymis", "neoplasm of epididymus", "neoplasm of epididymis", "Neoplasm of epididymis", "epididymis neoplasm (disease)", "Neoplasm of epididymis (disorder)", "neoplasm of epididymis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epididymal neoplasm", "shortest_name_length": 16}
{"curie": "UMLS:C0152233", "names": ["Fused Eyelid", "Fused eyelids", "Ankyloblepharon", "Blepharosynechia", "Ankyloblepharon totale", "Congenital ankyloblepharon", "Congenital Ankyloblepharon", "congenital ankyloblepharon", "Congenital ankyloblepharon (disorder)", "congenital ankyloblepharon (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital ankyloblepharon", "shortest_name_length": 12}
{"curie": "UMLS:C1335103", "names": ["Ocular Adnexal MALT lymphoma", "Ocular Adnexal Mucosa-Associated Lymphoid Tissue Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ocular Adnexal Mucosa-Associated Lymphoid Tissue Lymphoma", "shortest_name_length": 28}
{"curie": "UMLS:C5206801", "names": ["Locally Advanced Head and Neck Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Head and Neck Squamous Cell Carcinoma", "shortest_name_length": 54}
{"curie": "UMLS:C4526903", "names": ["Stage II Soft Tissue Sarcoma of the Trunk and Extremities", "Stage II Soft Tissue Sarcoma of the Trunk and Extremities AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Soft Tissue Sarcoma of the Trunk and Extremities AJCC v8", "shortest_name_length": 57}
{"curie": "UMLS:C5206480", "names": ["Locally Advanced Unresectable Rectal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Unresectable Rectal Adenocarcinoma", "shortest_name_length": 51}
{"curie": "MONDO:0008458", "names": ["SCA2", "ALS13", "SDSEM", "SCA 2", "OPCA2", "Wadia-Swami Syndrome", "Wadia Swami Syndrome", "Wadia-swami syndrome", "Wadia swami syndrome", "WADIA-SWAMI SYNDROME", "Swami Syndrome, Wadia", "Syndrome, Wadia-Swami", "Syndrome, Wadia Swami", "spinocerebellar ataxia 2", "SPINOCEREBELLAR ATAXIA 2", "Spinocerebellar Ataxia 2", "Spinocerebellar Ataxia-2", "Ataxia 2, Spinocerebellar", "Spinocerebellar Ataxia 2s", "Spinocerebellar Atrophy 2", "spinocerebellar atrophy 2", "Spinocerebellar Atrophy 2s", "Atrophy 2, Spinocerebellar", "Spinocerebellar Atrophy II", "SPINOCEREBELLAR ATROPHY II", "Spinocerebellar Atrophy IIs", "Atrophy 2s, Spinocerebellar", "Atrophy IIs, Spinocerebellar", "Type 2 Spinocerebellar Ataxia", "Spinocerebellar ataxia type 2", "spinocerebellar ataxia type 2", "Spinocerebellar Ataxia Type 2", "Olivopontocerebellar Atrophy 2", "olivopontocerebellar atrophy 2", "Olivopontocerebellar Atrophy 2s", "Olivopontocerebellar Atrophy II", "OLIVOPONTOCEREBELLAR ATROPHY II", "Atrophy 2, Olivopontocerebellar", "Olivopontocerebellar Atrophy IIs", "Atrophy II, Olivopontocerebellar", "Atrophy 2s, Olivopontocerebellar", "amyotrophic lateral sclerosis 13", "spinocerebellar ataxia Cuban type", "SPINOCEREBELLAR ATAXIA, CUBAN TYPE", "spinocerebellar ataxia, Cuban type", "Spinocerebellar Ataxia, Cuban Type", "amyotrophic lateral sclerosis type 13", "Spinocerebellar ataxia type 2 (disorder)", "olivopontocerebellar atrophy Holguin type", "OLIVOPONTOCEREBELLAR ATROPHY, HOLGUIN TYPE", "Olivopontocerebellar Atrophy, Holguin Type", "olivopontocerebellar atrophy, Holguin type", "Spinocerebellar Ataxia with Slow Eye Movements", "spinocerebellar ataxia with slow eye movements", "CEREBELLAR DEGENERATION WITH SLOW EYE MOVEMENTS", "cerebellar Degeneration with slow eye movements", "Cerebellar Degeneration with Slow Eye Movements", "ATXN2 autosomal dominant cerebellar ataxia type I", "AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 13", "Spinocerebellar Degeneration with Slow Eye Movements", "spinocerebellar Degeneration with slow eye movements", "amyotrophic lateral sclerosis, susceptibility to, 13", "SPINOCEREBELLAR DEGENERATION WITH SLOW EYE MOVEMENTS", "autosomal dominant cerebellar ataxia type I caused by mutation in ATXN2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia type 2", "shortest_name_length": 4}
{"curie": "MONDO:0008770", "names": ["AI1C", "amelogenesis imperfecta type IC", "amelogenesis imperfecta type 1C", "Amelogenesis Imperfecta, Type Ic", "AMELOGENESIS IMPERFECTA, TYPE IC", "amelogenesis imperfecta, type 1C", "amelogenesis imperfecta, type IC", "autosomal recessive amelogenesis imperfecta local hypoplastic type", "amelogenesis imperfecta, local hypoplastic type, autosomal recessive", "Amelogenesis Imperfecta, Local Hypoplastic Type, Autosomal Recessive", "AMELOGENESIS IMPERFECTA, LOCAL HYPOPLASTIC TYPE, AUTOSOMAL RECESSIVE", "autosomal recessive amelogenesis imperfecta hypoplastic with or without openbite malocclusion", "amelogenesis imperfecta, hypoplastic, with or without Openbite malocclusion, autosomal recessive", "Amelogenesis Imperfecta, Hypoplastic, With Or Without Openbite Malocclusion, Autosomal Recessive", "AMELOGENESIS IMPERFECTA, HYPOPLASTIC, WITH OR WITHOUT OPEN-BITE MALOCCLUSION, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amelogenesis imperfecta type 1C", "shortest_name_length": 4}
{"curie": "UMLS:C2047937", "names": ["Ill-defined disease", "Ill-defined disorder", "ill-defined condition", "Ill-defined condition", "Ill-defined disorder NOS", "ill-defined condition (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ill-defined disorder", "shortest_name_length": 19}
{"curie": "MONDO:0013090", "names": ["Del(19)(q13.11)", "monosomy 19q13.11", "Monosomy 19q13.11", "19q13.11 microdeletion syndrome", "Chromosome 19q13.11 Deletion Syndrome", "chromosome 19q13.11 deletion syndrome", "19q13.11 microdeletion syndrome (disorder)", "19q13.11 microdeletion syndrome (diagnosis)", "chromosome 19Q13.11 deletion syndrome, distal", "chromosome 19q13.11 deletion syndrome, distal", "deletion of part of chromosome 19 19q13.11 microdeletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 19q13.11 deletion syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0012607", "names": ["ASRT5", "asthma susceptibility 5", "IRAK3 inherited susceptibility to asthma", "ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 5", "asthma-related traits, susceptibility to, 5", "asthma-related traits, susceptibility to, type 5", "inherited susceptibility to asthma caused by mutation in IRAK3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "asthma-related traits, susceptibility to, 5", "shortest_name_length": 5}
{"curie": "UMLS:C4687630", "names": ["Refractory Central Nervous System Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Central Nervous System Non-Hodgkin Lymphoma", "shortest_name_length": 54}
{"curie": "MONDO:0002973", "names": ["Epithelioid Melanoma", "epithelioid melanoma", "epithelioid cell melanoma", "Epithelioid cell melanoma", "Epithelioid Cell Melanoma", "Epithelioid cell melanosarcoma", "Epithelioid Cell Malignant Melanoma", "epithelioid cell malignant melanoma", "epithelioid cell melanoma (morphologic abnormality)", "Epithelioid cell melanoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epithelioid cell melanoma", "shortest_name_length": 20}
{"curie": "UMLS:C1332168", "names": ["Colonic Adenoma with Intramucosal Adenocarcinoma", "Adenoma of Colon with Intramucosal Adenocarcinoma", "Adenoma of the Colon with Intramucosal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenoma of the Colon with Intramucosal Adenocarcinoma", "shortest_name_length": 48}
{"curie": "MONDO:0800098", "names": ["RP33", "RP 33", "retinitis pigmentosa 33", "retinitis pigmentosa type 33", "SNRNP200 retinitis pigmentosa", "SNRNP200-related dominant retinopathy", "retinitis pigmentosa caused by mutation in SNRNP200"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SNRNP200-related dominant retinopathy", "shortest_name_length": 4}
{"curie": "MONDO:0004479", "names": ["malignant pediatric germ cell tumor", "Malignant Pediatric Germ Cell Tumor", "malignant childhood germ cell tumor", "Childhood Malignant Germ Cell Tumor", "malignant pediatric germ cell neoplasm", "Malignant Pediatric Germ Cell Neoplasm", "Malignant Childhood Germ Cell Neoplasm", "malignant childhood germ cell neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant childhood germ cell neoplasm", "shortest_name_length": 35}
{"curie": "MONDO:0016089", "names": ["infantile Krabbe disease", "Krabbe disease, early-onset", "Krabbe disease, classic form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile Krabbe disease", "shortest_name_length": 24}
{"curie": "UMLS:C4745013", "names": ["Recurrent Acute Myeloid Leukemia Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Acute Myeloid Leukemia Not Otherwise Specified", "shortest_name_length": 56}
{"curie": "MONDO:0000497", "names": ["pyometra", "PYOMETRA", "Pyometra", "Pyometras", "Pyometrium", "pyometrium", "Pyometritis", "pyometritis", "Pyometra (disorder)", "pyometra (diagnosis)", "Pyometritis (diagnosis)", "myometrium inflammation", "inflammation of myometrium", "inflammatory disease of uterus pyometritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyometritis", "shortest_name_length": 8}
{"curie": "MONDO:0010879", "names": ["CODAS SYNDROME", "CODAS syndrome", "Codas Syndrome", "Cerebrooculodentoauriculoskeletal syndrome", "cerebrooculodentoauriculoskeletal syndrome", "cerebro-oculo-dento-auriculo-skeletal syndrome", "Cerebro-oculo-dento-auriculo-skeletal syndrome", "cerebro-oculo-dento-auriculo-skeletal (CODAS) syndrome", "CODAS (cerebro-oculo-dento-auriculo-skeletal) syndrome", "Cerebro-oculo-dento-auriculo-skeletal syndrome (disorder)", "cerebral, ocular, dental, auricular, and skeletal syndrome", "Cerebral, ocular, dental, auricular, and skeletal syndrome", "Cerebral, Ocular, Dental, Auricular, Skeletal Anomalies Syndrome", "cerebral, ocular, dental, auricular, and skeletal anomalies syndrome", "CEREBRAL, OCULAR, DENTAL, AURICULAR, AND SKELETAL ANOMALIES SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CODAS syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0017313", "names": ["disorder of folate metabolism and transport"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of folate metabolism and transport", "shortest_name_length": 43}
{"curie": "UMLS:C3887677", "names": ["Suppurative Granuloma", "suppurative; granuloma", "granuloma; suppurative"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Suppurative Granuloma", "shortest_name_length": 21}
{"curie": "UMLS:C0280958", "names": ["Sexual Dysfunction and Infertility", "dysfunction and infertility, sexual"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sexual Dysfunction and Infertility", "shortest_name_length": 34}
{"curie": "MONDO:0010340", "names": ["ASPGX1", "susceptibility to X-linked asperger syndrome 1", "ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1", "ASPERGER syndrome, X-linked, susceptibility to, 1", "Asperger syndrome, X-linked, susceptibility to, 1", "Asperger syndrome, X-linked, susceptibility to, type 1", "ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1 (disorder)", "Asperger syndrome susceptibility, X-linked 1, Isolated cases, X-linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Asperger syndrome, X-linked, susceptibility to, 1", "shortest_name_length": 6}
{"curie": "MONDO:0009286", "names": ["absence of gluteal muscle", "gluteal muscle, absence of", "gluteal muscles, absence of", "GLUTEAL MUSCLES, ABSENCE OF", "Congenital absence of gluteal muscles", "congenital absence of gluteal muscles"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gluteal muscles, absence of", "shortest_name_length": 25}
{"curie": "UMLS:C0751292", "names": ["Age-Related Memory Disorder", "Memory Disorder, Age-Related", "Age Related Memory Disorders", "Age-Related Memory Disorders", "Memory Disorders, Age-Related", "Memory Disorders, Age Related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Age-Related Memory Disorders", "shortest_name_length": 27}
{"curie": "MONDO:0003766", "names": ["Thalamus Tumor", "Thalamic Tumor", "thalamic cancer", "Thalamic Tumors", "Thalamus Tumors", "Thalamic Neoplasm", "thalamic neoplasm", "tumor of thalamus", "tumor of Thalamus", "Thalamus Neoplasm", "Tumor of Thalamus", "Thalamic Neoplasms", "Thalamus Neoplasms", "neoplasm of thalamus", "Neoplasm of Thalamus", "Tumor of the Thalamus", "Malignant Thalamus Tumor", "malignant thalamic tumor", "Malignant Thalamic Tumor", "malignant thalamus tumor", "Neoplasm of the Thalamus", "malignant thalamic tumors", "malignant thalamus tumors", "Malignant Thalamus Tumors", "Malignant Thalamic Tumors", "malignant thalamus neoplasm", "malignant tumor of Thalamus", "malignant thalamic neoplasm", "Malignant Thalamus Neoplasm", "Malignant Thalamic Neoplasm", "Malignant Tumor of Thalamus", "malignant tumor of thalamus", "malignant thalamus neoplasms", "Malignant Thalamus Neoplasms", "malignant thalamic neoplasms", "Malignant Thalamic Neoplasms", "Malignant neoplasm of thalamus", "Malignant Neoplasm of Thalamus", "malignant neoplasm of thalamus", "malignant tumor of the thalamus", "Malignant Tumor of the Thalamus", "neoplasm of thalamus (diagnosis)", "malignant neoplasm of the thalamus", "Malignant Neoplasm of the Thalamus", "dorsal plus ventral thalamus cancer", "cancer of dorsal plus ventral thalamus", "Malignant neoplasm of thalamus (disorder)", "malignant neoplasm of thalamus (diagnosis)", "malignant dorsal plus ventral thalamus neoplasm", "malignant neoplasm of dorsal plus ventral thalamus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thalamic cancer", "shortest_name_length": 14}
{"curie": "MONDO:0009409", "names": ["HYPERVITAMINOSIS A, SUSCEPTIBILITY TO", "hypervitaminosis a, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypervitaminosis a, susceptibility to", "shortest_name_length": 37}
{"curie": "MONDO:0020018", "names": ["cranial malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cranial malformation", "shortest_name_length": 20}
{"curie": "UMLS:C1336352", "names": ["Stage IVA Mouth Mucoepidermoid Carcinoma", "Stage IVA Mucoepidermoid Carcinoma of Mouth", "Stage IVA Oral Cavity Mucoepidermoid Cancer", "Stage IVA Oral Cavity Mucoepidermoid Carcinoma", "Stage IVA Mucoepidermoid Carcinoma of the Mouth", "Stage IVA Mucoepidermoid Carcinoma of Oral Cavity", "Stage IVA Mucoepidermoid Carcinoma of the Oral Cavity", "Stage IVA Oral Cavity Mucoepidermoid Carcinoma AJCC v6", "Stage IVA Oral Cavity Mucoepidermoid Carcinoma AJCC v7", "Stage IVA Oral Cavity Mucoepidermoid Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Oral Cavity Mucoepidermoid Carcinoma AJCC v6 and v7", "shortest_name_length": 40}
{"curie": "UMLS:C0404478", "names": ["ovarian cyst rupture", "OVARIAN CYST RUPTURE", "rupture ovarian cyst", "cyst ovarian rupture", "cyst ovarian ruptures", "cyst ovarian ruptured", "cysts ovarian rupture", "ruptured ovarian cyst", "Ovarian cyst ruptured", "Ruptured ovarian cyst", "Ruptured cyst of ovary", "cysts ovarian ruptured", "ruptured cyst of ovary", "cyst ovarian rupturing", "cysts ovarian ruptures", "Rupture of ovarian cyst", "rupture of ovarian cyst", "Ruptured ovarian cyst, NOS", "Ruptured cyst of ovary (disorder)", "ruptured cyst of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ruptured cyst of ovary", "shortest_name_length": 20}
{"curie": "UMLS:C2981632", "names": ["Stage 0 Hilar Cholangiocarcinoma", "Stage 0 Hilar Cholangiocarcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Hilar Cholangiocarcinoma AJCC v7", "shortest_name_length": 32}
{"curie": "UMLS:C3642433", "names": ["Relapsed Uterine Corpus Sarcoma", "Recurrent Uterine Corpus Sarcoma", "Relapsed Sarcoma of Uterine Corpus", "Recurrent Sarcoma of Uterine Corpus", "Relapsed Sarcoma of the Uterine Corpus", "Recurrent Sarcoma of the Uterine Corpus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Uterine Corpus Sarcoma", "shortest_name_length": 31}
{"curie": "MONDO:0004901", "names": ["Orofacial dyskinesia", "orofacial dyskinesia", "OROFACIAL DYSKINESIA", "Orofacial Dyskinesia", "orofacial; dyskinesia", "Orofacial Dyskinesias", "Dyskinesia, Orofacial", "oro-facial dyskinesia", "dyskinesia; orofacial", "Oro-facial dyskinesia", "Orofacial dyskinesias", "Oral-Facial Dyskinesia", "Oral Facial Dyskinesia", "Dyskinesias, Orofacial", "Dyskinesia, Oral-Facial", "Oral-Facial Dyskinesias", "Linguofacial Dyskinesia", "Tardive Oral Dyskinesia", "Dyskinesias, Oral-Facial", "Dyskinesia, Linguofacial", "Tardive Oral Dyskinesias", "Linguofacial Dyskinesias", "Dyskinesias, Linguofacial", "Orofacial dyskinesia (disorder)", "lingual-facial-buccal dyskinesia", "Lingual Facial Buccal Dyskinesia", "orofacial dyskinesia (diagnosis)", "Lingual-Facial-Buccal Dyskinesia", "Lingual-Facial-Buccal Dyskinesias", "Dyskinesia, Lingual-Facial-Buccal", "Dyskinesias, Lingual-Facial-Buccal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lingual-facial-buccal dyskinesia", "shortest_name_length": 20}
{"curie": "MONDO:0002236", "names": ["Eye Tumor", "Eye tumor", "eye tumor", "tumor eye", "eye tumour", "eye cancer", "cancer eye", "eye tumors", "Eye Cancer", "Eye tumour", "cancer eyes", "eye cancers", "eye tumours", "eyes tumors", "cancers eye", "Eye Cancers", "eyes cancer", "Eye--Cancer", "Cancer, Eye", "Eye--Tumors", "Eye Neoplasm", "ocular tumor", "Tumor of Eye", "Neoplasm;eye", "Cancers, Eye", "Ocular tumor", "eye neoplasm", "Tumor of eye", "of eye tumor", "Ocular Tumor", "ocular cancer", "Cancer of Eye", "Tumour of eye", "cancer of eye", "Neoplasm, Eye", "of eye cancer", "eye neoplasms", "Eye Neoplasms", "Neoplasms, Eye", "Neoplasm of eye", "Ocular Neoplasm", "Ocular neoplasm", "Neoplasm of Eye", "neoplasm of eye", "Tumor of the Eye", "Ocular neoplasms", "Neoplasm eye NOS", "Cancer of the Eye", "cancer of the eye", "Neoplasm malig;eye", "Neoplasm of the Eye", "malignant eye tumor", "neoplasm of eyeball", "Neoplasm of the eye", "Malignant Eye Tumor", "neoplasm of the eye", "eye malignant tumors", "Neoplasia of the eye", "eye cancer (diagnosis)", "neoplasm of eye proper", "Malignant Ocular Tumor", "malignant ocular tumor", "malignant tumor of eye", "Neoplasm of eye proper", "Malignant Tumor of Eye", "Malignant Eye Neoplasm", "Malignant tumor of eye", "malignant eye neoplasm", "eye neoplasm, malignant", "Eye Neoplasm, Malignant", "Malignant tumour of eye", "malignant ocular neoplasm", "Malignant neoplasm of eye", "Malignant Ocular Neoplasm", "Malignant eye cancer, NOS", "malignant neoplasm of eye", "Malignant Neoplasm of Eye", "Malignant Tumor of the Eye", "malignant tumor of the eye", "Malignant eye neoplasm NOS", "neoplasm of eye (diagnosis)", "Malignant Neoplasm of the Eye", "malignant neoplasm of the eye", "Malignant neoplasm of eye, NOS", "malignant neosplasm of the eye", "neoplasm of eyeball (diagnosis)", "eyeball of camera-type eye cancer", "Neoplasm of eye proper (disorder)", "Malignant tumor of eye (disorder)", "cancer of eyeball of camera-type eye", "malignant neoplasm of eye (diagnosis)", "Malignant neoplasm of eye, unspecified", "Malignant neoplasm of eye, part unspecified", "Malignant neoplasm of unspecified site of eye", "malignant eyeball of camera-type eye neoplasm", "malignant neoplasm of eyeball of camera-type eye", "Malignant neoplasm of other specified sites of eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ocular cancer", "shortest_name_length": 9}
{"curie": "UMLS:C0347484", "names": ["Benign Broad Ligament Neoplasm", "benign broad ligament neoplasm", "benign tumor of broad ligament", "Benign neoplasm of broad ligament", "benign neoplasm of broad ligament", "Benign neoplasm of broad ligament (disorder)", "benign neoplasm of broad ligament (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign neoplasm of broad ligament", "shortest_name_length": 30}
{"curie": "MONDO:0012980", "names": ["ECO", "ECO syndrome", "endocrine-CEREBROOSTEODYSPLASIA", "Endocrine-Cerebroosteodysplasia", "ENDOCRINE-CEREBROOSTEODYSPLASIA", "Endocrine cerebroosteodysplasia syndrome", "Endocrine-cerebro-osteodysplasia syndrome", "endocrine-cerebro-osteodysplasia syndrome", "ECO (endocrine-cerebro-osteodysplasia) syndrome", "Endocrine-cerebro-osteodysplasia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endocrine-cerebro-osteodysplasia syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C5206604", "names": ["Paratesticular Schwannoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paratesticular Schwannoma", "shortest_name_length": 25}
{"curie": "MONDO:0011723", "names": ["HMH", "HEMIFACIAL MYOHYPERPLASIA", "hemifacial myohyperplasia", "Hemifacial myohyperplasia", "Hemifacial myohyperplasia (disorder)", "Hypertrophy and asymmetry of the facial muscles", "hypertrophy and asymmetry of the facial muscles"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemifacial myohyperplasia", "shortest_name_length": 3}
{"curie": "MONDO:0042965", "names": ["azorean disease, type V", "Machado-Joseph disease type 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Machado-Joseph disease type 5", "shortest_name_length": 23}
{"curie": "UMLS:C0751019", "names": ["Carotid territory transient ischemic attack", "Carotid territory transient ischaemic attack", "Carotid Circulation Transient Ischemic Attack", "Transient Ischemic Attack, Carotid Circulation", "Anterior Circulation Transient Ischemic Attack", "Anterior circulation transient ischemic attack", "Transient Ischemic Attack, Anterior Circulation", "Anterior circulation transient ischaemic attack", "transient ischemic attack of anterior circulation", "Carotid territory transient ischemic attack (disorder)", "transient ischemic attack of anterior circulation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carotid Circulation Transient Ischemic Attack", "shortest_name_length": 43}
{"curie": "MONDO:0007204", "names": ["CLCRP1", "COLE-CARPENTER SYNDROME 1", "Cole-Carpenter syndrome 1", "COLE-CARPENTER syndrome 1", "P4HB Cole-Carpenter syndrome", "Cole-Carpenter syndrome type 1", "Cole-Carpenter syndrome caused by mutation in P4HB", "bone fragility with craniosynostosis, ocular proptosis, hydrocephalus, and distinctive Facial features", "BONE FRAGILITY WITH CRANIOSYNOSTOSIS, OCULAR PROPTOSIS, HYDROCEPHALUS, AND DISTINCTIVE FACIAL FEATURES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cole-Carpenter syndrome 1", "shortest_name_length": 6}
{"curie": "MONDO:0030042", "names": ["PROCHOB", "proteinuria, chronic benign", "PROTEINURIA, CHRONIC BENIGN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "proteinuria, chronic benign", "shortest_name_length": 7}
{"curie": "UMLS:C1516072", "names": ["Astler-Coller C2 Colorectal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Astler-Coller C2 Colorectal Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0000234", "names": ["maculatum infection", "Rickettsia parkeri spotted fever"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rickettsia parkeri spotted fever", "shortest_name_length": 19}
{"curie": "MONDO:0014652", "names": ["EVR6", "EXUDATIVE VITREORETINOPATHY 6", "exudative vitreoretinopathy 6", "exudative vitreoretinopathy type 6", "ZNF408 exudative vitreoretinopathy", "exudative vitreoretinopathy caused by mutation in ZNF408"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exudative vitreoretinopathy 6", "shortest_name_length": 4}
{"curie": "MONDO:0001539", "names": ["retina hole", "retina tear", "hole retina", "Torn retina", "tear retina", "retina tears", "RETINAL TEAR", "holes retina", "Retinal Hole", "tear; retina", "Retinal Tear", "hole retinal", "retinal tear", "retinal hole", "Retinal tear", "retina; tear", "Retinal Tears", "Retinal tears", "Tear, Retinal", "retinal break", "Retinal Break", "Hole, Retinal", "Retinal break", "retinal tears", "Retinal Holes", "retinal holes", "Retinal Breaks", "Retinal defect", "Holes, Retinal", "Break, Retinal", "Retinal Defect", "Tears, Retinal", "retinal breaks", "retinal defects", "Breaks, Retinal", "Retinal Dialyse", "Retinal dialysis", "Retinal Dialyses", "defect of retina", "retinal dialysis", "Retinal tear, NOS", "Dialyses, Retinal", "Retinal break NOS", "Retinal break, NOS", "Retinal breaks NOS", "Retinal defect, NOS", "Retinal perforation", "Retinal Perforation", "retinal perforation", "Perforation, Retinal", "Retinal Perforations", "retinal perforations", "Perforations, Retinal", "Retinal tear (disorder)", "retinal tear (diagnosis)", "Retinal defect (disorder)", "unspecified retinal defect", "Retinal dialysis (disorder)", "Retinal defect, unspecified", "defect of retina (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal perforation", "shortest_name_length": 11}
{"curie": "MONDO:0013688", "names": ["PCZH", "LWNH", "Becker Nevus", "Becker's Nevus", "Becker's nevus", "Becker's naevus", "Melanosis Neviformis", "melanosis Neviformis", "zebra-like hyperpigmentation", "zosteriform lentiginous nevus", "pigmented hairy nevus; Becker", "Becker; pigmented hairy nevus", "zosteriform hyperpigmentation", "Pigmented Hairy Nevus of Becker", "Pigmented hairy nevus of Becker", "pigmented hairy Nevus of Becker", "Pigmented hairy epidermal nevus", "Pigmented Hairy Epidermal Nevus", "pigmented hairy Epidermal Nevus", "Pigmented hairy epidermal naevus", "Pigmented hairy naevus of Becker", "linear and whorled hypermelanosis", "reticulate hyperpigmentation of Iijima", "linear and whorled nevoid hypermelanosis", "Linear and whorled nevoid hypermelanosis", "NEVOID HYPERMELANOSIS, LINEAR AND WHORLED", "Pigmented hairy epidermal nevus of Becker", "nevoid hypermelanosis, linear and whorled", "Linear and whorled naevoid hypermelanosis", "Pigmented hairy epidermal nevus (disorder)", "Linear papular ectodermal-mesodermal hamartoma", "linear papular ectodermal-mesodermal hamartoma", "Linear Papular Ectodermal-Mesodermal Hamartoma", "Linear and whorled nevoid hypermelanosis (disorder)", "Progressive cribriform and zosteriform hyperpigmentation", "Progressive Cribriform and Zosteriform Hyperpigmentation", "progressive cribriform and zosteriform hyperpigmentation", "HYPERPIGMENTATION, PROGRESSIVE CRIBRIFORM AND ZOSTERIFORM", "hyperpigmentation, progressive cribriform and zosteriform", "PCZH - progressive cribriform and zosteriform hyperpigmentation", "Progressive cribriform and zosteriform hyperpigmentation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "linear and whorled nevoid hypermelanosis", "shortest_name_length": 4}
{"curie": "MONDO:0007385", "names": ["SCAD", "idiopathic SCAD", "coronary artery dissection", "Coronary artery dissection", "artery coronary dissections", "Dissection of coronary artery", "dissection of coronary artery", "Spontaneous Coronary Artery Dissection", "coronary artery dissection, spontaneous", "Coronary Artery Dissection, Spontaneous", "CORONARY ARTERY DISSECTION, SPONTANEOUS", "Dissection of coronary artery (disorder)", "dissection of coronary artery (diagnosis)", "idiopathic spontaneous coronary artery dissection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic spontaneous coronary artery dissection", "shortest_name_length": 4}
{"curie": "MONDO:0007824", "names": ["Missing lower central incisor", "Absence of lower central incisor", "Missing mandibular central incisor", "incisors, lower central, absence of", "INCISORS, LOWER CENTRAL, ABSENCE OF", "Absence of mandibular central incisor", "Agenesis of mandibular central incisor", "Failure of development of mandibular central incisor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "incisors, lower central, absence of", "shortest_name_length": 29}
{"curie": "UMLS:C1333111", "names": ["Colorectal Inflammatory Polyp", "Large Bowel Inflammatory Polyp", "Inflammatory Polyp of Large Bowel", "Large Intestinal Inflammatory Polyp", "Inflammatory Polyp of the Large Bowel"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Inflammatory Polyp", "shortest_name_length": 29}
{"curie": "MONDO:0012639", "names": ["IDMDC", "SPG18", "spastic paraplegia 18", "hereditary spastic paraplegia 18", "hereditary spastic paraplegia type 18", "autosomal recessive spastic paraplegia 18", "SPASTIC PARAPLEGIA 18, AUTOSOMAL RECESSIVE", "Spastic Paraplegia 18, Autosomal Recessive", "spastic paraplegia 18, autosomal recessive", "Autosomal recessive spastic paraplegia type 18", "autosomal recessive spastic paraplegia type 18", "ERLIN2 autosomal recessive complex spastic paraplegia", "Autosomal recessive spastic paraplegia type 18 (disorder)", "intellectual disability, motor dysfunction and joint contractures", "intellectual disability, motor dysfunction, and Joint contractures", "Intellectual Disability, Motor Dysfunction, and Joint Contractures", "INTELLECTUAL DISABILITY, MOTOR DYSFUNCTION, AND JOINT CONTRACTURES", "autosomal recessive complex spastic paraplegia caused by mutation in ERLIN2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 18", "shortest_name_length": 5}
{"curie": "MONDO:0016993", "names": ["peeling skin syndrome type C", "generalized deciduous skin type C", "generalized peeling skin syndrome type C"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "generalized peeling skin syndrome type C", "shortest_name_length": 28}
{"curie": "UMLS:C2064425", "names": ["Extrahepatic Bile Duct Tubulopapillary Adenoma", "tubulopapillary adenoma of extrahepatic bile duct", "tubulopapillary adenoma of extrahepatic bile duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tubulopapillary adenoma of extrahepatic bile duct", "shortest_name_length": 46}
{"curie": "UMLS:C2984903", "names": ["Pericardial Adenomatoid Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pericardial Adenomatoid Tumor", "shortest_name_length": 29}
{"curie": "UMLS:C4744445", "names": ["Smoldering Waldenstrom Macroglobulinemia", "Asymptomatic Waldenstrom Macroglobulinemia", "Smoldering (Asymptomatic) Waldenstrom Macroglobulinemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Smoldering Waldenstrom Macroglobulinemia", "shortest_name_length": 40}
{"curie": "UMLS:C0278818", "names": ["recurrent adrenocortical cancer", "Recurrent Adrenal Cortex Cancer", "Relapsed Adrenocortical Carcinoma", "Relapsed Adrenal Cortex Carcinoma", "recurrent adrenal cortex carcinoma", "Recurrent Adrenocortical Carcinoma", "Recurrent Adrenal Cortex Carcinoma", "adrenocortical carcinoma, recurrent", "carcinoma, adrenocortical recurrent", "Relapsed Carcinoma of Adrenal Cortex", "Recurrent Adrenal Cortical Carcinoma", "Recurrent Carcinoma of Adrenal Cortex", "Relapsed Carcinoma of the Adrenal Cortex", "Recurrent Carcinoma of the Adrenal Cortex"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Adrenal Cortical Carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0004461", "names": ["vaginal tubular adenoma", "Vaginal Tubulovillous Adenoma", "vaginal tubulovillous adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vaginal tubulovillous adenoma", "shortest_name_length": 23}
{"curie": "UMLS:C5418595", "names": ["Refractory Cervical Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Cervical Carcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0010134", "names": ["PDS", "TDH2B", "Pendred", "GDTH IIB", "PENDRED SYNDROME", "Pendred Syndrome", "Pendred syndrome", "pendred syndrome", "pendreds syndrome", "pendred's syndrome", "Pendred's Syndrome", "Pendred's syndrome", "Deafness with goiter", "deafness with goiter", "DEAFNESS WITH GOITER", "Goitre-deafness syndrome", "Goiter-deafness syndrome", "goiter-deafness syndrome", "GOITER-DEAFNESS SYNDROME", "syndrome; goiter-deafness", "goiter-deafness; syndrome", "Thyroid Dyshormonogenesis 2B", "THYROID DYSHORMONOGENESIS 2B", "thyroid dyshormonogenesis 2B", "Goiter-hearing loss syndrome", "Pendred's syndrome (disorder)", "thyroid dyshormonogenesis, TDH2B", "Thyroid hormone organification defect II B", "Hypothyroidism with sensorineural deafness", "genetic defect in thyroid hormonogenesis 2B", "thyroid dyshormonogenesis, TDH2B (diagnosis)", "Genetic defect in thyroid hormonogenesis II B", "THYROID HORMONOGENESIS, GENETIC DEFECT IN, 2B", "Thyroid Hormonogenesis, Genetic Defect In, 2B", "thyroid hormonogenesis, genetic defect in, 2B", "congenital hypothyroidism due to dyshormonogenesis 2B", "hypothyroidism, congenital, due to dyshormonogenesis, 2B", "Hypothyroidism, Congenital, Due To Dyshormonogenesis, 2B", "HYPOTHYROIDISM, CONGENITAL, DUE TO DYSHORMONOGENESIS, 2B", "Autosomal Recessive Sensorineural Hearing Impairment and Goiter", "autosomal recessive sensorineural hearing impairment and goiter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pendred syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C5419526", "names": ["Metastatic Ovarian Undifferentiated Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Ovarian Undifferentiated Carcinoma", "shortest_name_length": 45}
{"curie": "MONDO:0019861", "names": ["thyroid hypoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid hypoplasia", "shortest_name_length": 18}
{"curie": "MONDO:0020022", "names": ["nerve; anomaly", "anomaly; nerve", "Nervous System Anomaly", "nervous system; anomaly", "anomaly; nervous system", "Anomaly, Nervous System", "Neurologic abnormalities", "Nervous System Anomalies", "Neurological abnormality", "deformity; nervous system", "nervous system; deformity", "Anomalies, Nervous System", "Nervous System Abnormality", "Congenital anomaly;nerv sys", "Nervous System Malformation", "Abnormality, Nervous System", "Nervous System Abnormalities", "Malformation, Nervous System", "Nervous System Malformations", "Malformations, Nervous System", "Nervous system--Abnormalities", "Abnormalities, Nervous System", "Brain and/or spinal cord issue", "Congenital neurologic anomalies", "Congenital anomaly neurological", "Abnormality of the nervous system", "Congenital Nervous System Disorder", "congenital nervous system disorder", "Nervous system congenital anomalies", "Congenital lesion of nervous system", "central nervous system malformation", "nervous system; disorder, congenital", "Congenital disease of nervous system", "Congenital anomaly of nervous system", "Congenital Anomalies, Nervous System", "Congenital deformity of nervous system", "Nervous System Congenital Malformations", "Nervous System Congenital Abnormalities", "congenital malformations nervous system", "Congenital anomaly NOS of nervous system", "congenital anomaly of the nervous system", "Congenital Malformations, Nervous System", "Congenital Abnormalities, Nervous System", "Congenital lesion of nervous system, NOS", "Nervous System Malformations, Congenital", "Malformations, Nervous System, Congenital", "Abnormalities, Congenital, Nervous System", "Congenital anomaly of nervous system, NOS", "Congenital disease of nervous system, NOS", "Congenital deformity NOS of nervous system", "CONGENITAL ANOMALIES OF THE NERVOUS SYSTEM", "congenital malformations of nervous system", "Congenital deformity of nervous system, NOS", "Congenital malformation of the nervous system", "Congenital malformations of the nervous system", "Congenital anomaly of nervous system (disorder)", "disease (or disorder); nervous system, congenital", "Congenital malformation of nervous system, unspecified", "congenital malformations of nervous system (diagnosis)", "Congenital malformations of the nervous system (Q00-Q07)", "CONGENITAL ANOMALIES OF THE NERVOUS SYSTEM: GENERAL TERMS", "Unspecified congenital anomaly of brain, spinal cord, and nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system malformation", "shortest_name_length": 14}
{"curie": "UMLS:C0023070", "names": ["laryngopharyngitis", "pharyngolaryngitis", "Pharyngolaryngitis", "Laryngopharyngitis", "Laryngopharyngitis NOS", "Pharyngolaryngitis (disorder)", "laryngopharyngitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pharyngolaryngitis", "shortest_name_length": 18}
{"curie": "MONDO:0006238", "names": ["GH cell adenoma", "Somatotrophinoma", "Somatotroph Adenoma", "somatotrope adenoma", "Somatotroph adenoma", "Somatotrope Adenoma", "somatotroph adenoma", "Somatotroph Adenomas", "somatotropic adenoma", "Adenoma, Somatotroph", "Adenomas, Somatotroph", "Somatotroph PitNET/Adenoma", "Somatotroph pituitary adenoma", "pituitary adenoma somatotroph", "GH Secreting Pituitary Adenoma", "Somatotroph adenoma (disorder)", "GH-Secreting Pituitary Adenoma", "Pituitary Adenoma, GH Secreting", "Pituitary Adenoma, GH-Secreting", "GH-Secreting Pituitary Adenomas", "Somatotroph adenoma (diagnosis)", "growth hormone-producing adenoma", "Pituitary Adenomas, GH-Secreting", "Acromegaly Due To Pituitary Adenoma", "Growth Hormone-Producing Pituitary Adenoma", "Pituitary Growth Hormone-Secreting Adenoma", "Pituitary Growth Hormone Secreting Adenoma", "Growth Hormone-Secreting Pituitary Adenoma", "growth hormone producing pituitary adenoma", "Growth hormone-secreting pituitary adenoma", "growth hormone secreting pituitary adenoma", "Growth Hormone Producing Pituitary Adenoma", "Somatotroph Pituitary Neuroendocrine Tumor", "Pituitary Adenoma, Growth Hormone Secreting", "Pituitary Adenoma, Growth Hormone-Secreting", "growth hormone secreting adenoma of pituitary", "growth hormone producing adenoma of pituitary", "Growth Hormone Secreting Adenoma of Pituitary", "Growth Hormone-Producing Pituitary Gland Tumor", "Growth Hormone-Producing Pituitary Gland Adenoma", "Growth Hormone Producing Pituitary Gland Adenoma", "growth hormone producing pituitary gland adenoma", "growth hormone secreting pituitary gland adenoma", "Growth Hormone Secreting Pituitary Gland Adenoma", "growth hormone-producing pituitary gland adenoma", "growth hormone secreting adenoma of the pituitary", "growth hormone producing adenoma of the pituitary", "Growth Hormone Producing adenoma of the Pituitary", "Somatotroph Pituitary Neuroendocrine Tumor/Adenoma", "Growth Hormone Producing Adenoma of Pituitary Gland", "growth hormone secreting adenoma of pituitary gland", "growth hormone producing adenoma of pituitary gland", "Growth Hormone Secreting Adenoma of Pituitary Gland", "Somatotroph pituitary adenoma (morphologic abnormality)", "growth hormone producing adenoma of the pituitary gland", "growth hormone secreting adenoma of the pituitary gland", "Growth Hormone Secreting Adenoma of the Pituitary Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "growth hormone-producing pituitary gland adenoma", "shortest_name_length": 15}
{"curie": "MONDO:0017025", "names": ["Langerhans cell histiocytosis", "Langerhans Cell Histiocytosis", "histiocytosis X specific to childhood", "childhood Langerhans cell histiocytosis", "Childhood Langerhans Cell Histiocytosis", "Langerhans cell histiocytosis specific to childhood", "Langerhans cell granulomatosis specific to childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Langerhans cell histiocytosis specific to childhood", "shortest_name_length": 29}
{"curie": "UMLS:C0477371", "names": ["Other epilepsy", "Other epilepsy NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Other epilepsy", "shortest_name_length": 14}
{"curie": "UMLS:C4763539", "names": ["Unresectable Skin Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Skin Squamous Cell Carcinoma", "shortest_name_length": 41}
{"curie": "UMLS:C4744711", "names": ["Scrotal Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Scrotal Sarcoma", "shortest_name_length": 15}
{"curie": "MONDO:0015088", "names": ["autosomal dominant pure HSP", "autosomal dominant pure SPG", "autosomal dominant uncomplicated SPG", "autosomal dominant uncomplicated HSP", "autosomal dominant pure spastic paraplegia", "autosomal dominant uncomplicated spastic paraplegia", "autosomal dominant pure hereditary spastic paraplegia", "pure hereditary spastic paraplegia, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant pure spastic paraplegia", "shortest_name_length": 27}
{"curie": "UMLS:C1333287", "names": ["Differentiated Granulocytic Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Differentiated Granulocytic Sarcoma", "shortest_name_length": 35}
{"curie": "MONDO:0020518", "names": ["Hashimoto-Pritzker disease", "Hashimoto-Pritzker syndrome", "Hashimoto-Pritzker histiocytosis", "Congenital self-healing histiocytosis", "congenital Langerhans cell histiocytosis", "Langerhans cell histiocytosis, Hashimoto-Pritzker type", "Langerhans cell histiocytosis - Hashimoto-Pritzker type", "Langerhans cell histiocytosis, Hashimoto-Pritzker type (diagnosis)", "Langerhans cell histiocytosis - Hashimoto-Pritzker type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hashimoto-Pritzker syndrome", "shortest_name_length": 26}
{"curie": "MONDO:0026731", "names": ["CHNG8", "congenital nongoitrous hypothyroidism 8", "hypothyroidism, congenital, nongoitrous, 8", "HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypothyroidism, congenital, nongoitrous, 8", "shortest_name_length": 5}
{"curie": "MONDO:0009924", "names": ["VDDI", "PDDRI", "VDDR1", "VDDR-I", "vitamin D-dependency type I", "vitamin D dependency, type 1", "1-alpha-hydroxylase deficiency", "1 Alpha-hydroxylase deficiency", "1 Alpha-hydroxylase Deficiency", "pseudovitamin D-deficient rickets", "vitamin D-dependent rickets type 1", "Vitamin D-dependent Rickets Type 1", "vitamin D dependent rickets type I", "Vitamin D-Dependent Rickets Type 1", "Pseudo Vitamin-D Deficient Rickets", "pseudo vitamin-D deficient rickets", "vitamin D-dependent rickets, type 1", "vitamin D 1 Alpha-Hydroxylase deficiency", "Vitamin D 1 Alpha-Hydroxylase Deficiency", "hypocalcemic vitamin D-dependent rickets", "Vitamin D Hydroxylation-deficient Rickets type 1a", "Vitamin D Hydroxylation-Deficient Rickets, Type 1A", "selective 1-alpha, 25-hydroxyvitamin D3 deficiency", "Selective 1-alpha, 25-hydroxyvitamin D3 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitamin D-dependent rickets, type 1", "shortest_name_length": 4}
{"curie": "MONDO:0019791", "names": ["MIRAS", "recessive mitochondrial ataxia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "recessive mitochondrial ataxia syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0043176", "names": ["PRPP synthetase deficiency", "deafness hyperuricemia neurologic ataxia", "Deafness hyperuricemia neurologic ataxia", "Deficiency of ribose-phosphate pyrophosphokinase", "Phosphoribosylpyrophosphate synthetase deficiency", "phosphoribosylpyrophosphate synthetase deficiency", "Deficiency of ribose-phosphate pyrophosphokinase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phosphoribosylpyrophosphate synthetase deficiency", "shortest_name_length": 26}
{"curie": "UMLS:C1334623", "names": ["Malignant Tumor of Superior Vena Cava", "Malignant Superior Vena Cava Neoplasm", "Malignant Neoplasm of Superior Vena Cava", "Malignant Tumor of the Superior Vena Cava", "Malignant Neoplasm of the Superior Vena Cava"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Superior Vena Cava Neoplasm", "shortest_name_length": 37}
{"curie": "MONDO:0003169", "names": ["diencephalic astrocytoma", "diencephalon astrocytoma", "Diencephalic Astrocytoma", "diencephalic astrocytomas", "Diencephalic Astrocytomas", "astrocytoma of diencephalon", "Astrocytoma of Diencephalon", "astrocytoma of Diencephalon", "Astrocytoma of the Diencephalon", "astrocytoma of the diencephalon", "diencephalon astrocytoma (excluding glioblastoma)", "astrocytoma (excluding glioblastoma) of diencephalon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diencephalic astrocytomas", "shortest_name_length": 24}
{"curie": "UMLS:C1335140", "names": ["Oropharynx Polyp", "Oropharyngeal Polyp", "Polyp of Oropharynx", "Polyp of the Oropharynx"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oropharyngeal Polyp", "shortest_name_length": 16}
{"curie": "MONDO:0019307", "names": ["GABEB", "JEB-I", "JEB1A", "JEN-nH", "JEB-nH gen", "JEB, generalized intermediate", "Adult junctional epidermolysis bullosa", "JUNCTIONAL EPIDERMOLYSIS BULLOSA INVERSA", "junctional epidermolysis bullosa, Disentis type", "Junctional epidermolysis bullosa non-Herlitz type", "junctional epidermolysis bullosa non-Herlitz type", "Adult junctional epidermolysis bullosa (disorder)", "Epidermolysis bullosa junctionalis, Disentis type", "generalized atrophic benign epidermolysis bullosa", "EPIDERMOLYSIS BULLOSA, JUNCTIONAL 1A, INTERMEDIATE", "junctional epidermolysis bullosa generalisata mitis", "Epidermolysis Bullosa, Junctional, Non-Herlitz Type", "EPIDERMOLYSIS BULLOSA JUNCTIONALIS, NON-HERLITZ TYPE", "Epidermolysis Bullosa Junctionalis, Non-Herlitz Type", "EPIDERMOLYSIS BULLOSA, JUNCTIONAL 1A, NON-HERLITZ TYPE", "junctional epidermolysis bullosa, generalized intermediate", "Junctional epidermolysis bullosa non-Herlitz type (disorder)", "generalized junctional epidermolysis bullosa non-Herlitz type", "EPIDERMOLYSIS BULLOSA, JUNCTIONAL 1A, GENERALIZED INTERMEDIATE", "generalized junctional epidermolysis bullosa, non-Herlitz type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "generalized junctional epidermolysis bullosa non-Herlitz type", "shortest_name_length": 5}
{"curie": "MONDO:0012496", "names": ["KDVS", "KdVS", "Koolen-de Vries syndrome", "Koolen-DE Vries syndrome", "Koolen-De Vries syndrome", "Koolen de Vries syndrome", "17q21.31 deletion syndrome", "microdeletion 17q21.31 syndrome", "microdeletion 17Q21.31 syndrome", "chromosome 17q21.31 deletion syndrome", "chromosome 17Q21.31 deletion syndrome", "chromosome 17q21.31 microdeletion syndrome", "KANSL1-related intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Koolen-de Vries syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0016115", "names": ["adult bulbospinal muscular atrophy", "bulbospinal muscular atrophy of adult", "bulbospinal muscular atrophy of adults", "bulbospinal muscular atrophy of adulthood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bulbospinal muscular atrophy of adulthood", "shortest_name_length": 34}
{"curie": "UMLS:C0086457", "names": ["Industrial Dermatoses", "Industrial Dermatosis", "Dermatosis, Industrial", "Dermatoses, Industrial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Industrial Dermatosis", "shortest_name_length": 21}
{"curie": "MONDO:0018107", "names": ["idiopathic recurrent and disabling cutaneous herpes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic recurrent and disabling cutaneous herpes", "shortest_name_length": 51}
{"curie": "UMLS:C4289035", "names": ["Gingival Spindle Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gingival Spindle Cell Carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0009279", "names": ["AAA", "AAAS", "3A syndrome", "4A syndrome", "2A syndrome", "Aaa Syndrome", "AAA syndrome", "Double A syndrome", "ALLGROVE SYNDROME", "TRIPLE-A SYNDROME", "triple-a syndrome", "Triple A Syndrome", "Allgrove syndrome", "Triple-A Syndrome", "triple a syndrome", "triple-A syndrome", "Triple-A syndrome", "allgrove syndrome", "triple A syndrome", "Triple A syndrome", "Allgrove Syndrome", "allgroves syndrome", "Quaternary A syndrome", "quaternary A syndrome", "Achalasia-Alacrima Syndrome", "achalasia-alacrima syndrome", "ACHALASIA-ALACRIMA SYNDROME", "achalasia alacrima syndrome", "Achalasia alacrimia syndrome", "hypoadrenalism with achalasia", "Addisonian-Achalasia Syndrome", "Hypoadrenalism with achalasia", "Achalasia-addisonian syndrome", "ADDISONIAN-ACHALASIA SYNDROME", "Addisonian achalasia syndrome", "Addisonian-achalasia syndrome", "HYPOADRENALISM WITH ACHALASIA", "Achalasia-Addisonian Syndrome", "Alacrima-Achalasia-Addisonianism", "ALACRIMA-ACHALASIA-ADDISONIANISM", "alacrima-achalasia-addisonianism", "Alacrimia-achalasia-addisonianism", "Infantile achalasia with alacrima", "Glucocorticoid deficiency and achalasia", "glucocorticoid deficiency and achalasia", "GLUCOCORTICOID DEFICIENCY AND ACHALASIA", "Glucocorticoid deficiency with achalasia", "glucocorticoid deficiency with achalasia", "Achalasia-Addisonianism-Alacrima Syndrome", "Achalasia-addisonianism-alacrima syndrome", "achalasia-addisonianism-alacrima syndrome", "ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME", "Achalasia-Addisonianism-Alacrimia syndrome", "Achalasia Addisonianism Alacrimia syndrome", "achalasia-addisonianism-alacrimia syndrome", "achalasia addisonianism alacrimia syndrome", "Adrenal insufficiency-achalasia-alacrima syndrome", "adrenal insufficiency-achalasia-alacrima syndrome", "Glucocorticoid deficiency with achalasia (disorder)", "glucocorticoid deficiency with achalasia (diagnosis)", "Alacrima-achalasia-adrenal insufficiency neurologic disorder", "ALACRIMA-ACHALASIA-ADRENAL INSUFFICIENCY NEUROLOGIC DISORDER", "Acth-Resistant Adrenal Insufficiency, Achalasia And Alacrima", "ACTH-resistant adrenal insufficiency, achalasia and alacrima", "alacrima-achalasia-adrenal insufficiency neurologic disorder", "ACTH resistant adrenal insufficiency, achalasia and alacrima", "ACTH-RESISTANT ADRENAL INSUFFICIENCY, ACHALASIA AND ALACRIMA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "triple-A syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0009589", "names": ["Reardon-Hall-Slaney syndrome", "Reardon Hall Slaney syndrome", "Mesomelic dysplasia, Reardon type", "mesomelic dysplasia, Reardon type", "MESOMELIC LIMB SHORTENING AND BOWING", "mesomelic limb shortening and bowing", "Mesomelic Limb Shortening and Bowing", "Mesomelic dysplasia, Kozlowski-Reardon type", "mesomelic dysplasia, Kozlowski-Reardon type", "mesomelic dwarfism cleft palate camptodactyly", "mesomelic dwarfism-cleft palate-camptodactyly syndrome", "Mesomelic dwarfism-cleft palate-camptodactyly syndrome", "Mesomelic dysplasia with cleft palate and camptodactyly syndrome", "Mesomelic dysplasia with cleft palate and camptodactyly syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mesomelic dwarfism-cleft palate-camptodactyly syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0035473", "names": ["WILD syndrome", "warts-immunodeficiency-lymphedema-anogenital dysplasia syndrome", "disseminated warts-impaired cell-mediated immunity-primary lymphedema-anogenital dysplasia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "warts-immunodeficiency-lymphedema-anogenital dysplasia syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0007282", "names": ["CTRCT29", "CATARACT 29", "cataract 29", "cataract type 29", "cataract 29 coralliform", "cataract 29, coralliform", "CATARACT 29, CORALLIFORM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 29", "shortest_name_length": 7}
{"curie": "UMLS:C1333852", "names": ["Grade 4 Clear Cell Renal Cell Carcinoma", "Grade 4 Conventional (Clear Cell) Renal Cell Carcinoma", "G4 Nuclei bizarre and multilobated, 20 um or greater, nucleoli prominent, chromatin clumped"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade 4 Clear Cell Renal Cell Carcinoma", "shortest_name_length": 39}
{"curie": "UMLS:C1963943", "names": ["Atherothrombosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atherothrombosis", "shortest_name_length": 16}
{"curie": "MONDO:0002279", "names": ["iron disorder", "Iron Disorder", "disorders iron", "iron metabolism disease", "IRON METABOLISM DISORDER", "metabolic disorder; iron", "iron; metabolic disorder", "Iron metabolism disorder", "Iron Metabolism Disorder", "iron metabolism disorder", "metabolism disorder, iron", "Metabolism Disorder, Iron", "disorder, iron metabolism", "Disorder, Iron Metabolism", "disorders iron metabolism", "Iron Metabolism Disorders", "metabolism disorders, iron", "Metabolism Disorders, Iron", "disorders, iron metabolism", "Disorders, Iron Metabolism", "Iron--Metabolism--Disorders", "disorder of iron metabolism", "Disorder of iron metabolism", "DISORDERS OF IRON METABOLISM", "Disorders of iron metabolism", "disorders of iron metabolism", "Disorder of iron metabolism, NOS", "iron metabolism disorder (diagnosis)", "Disorder of iron metabolism (disorder)", "Disorder of iron metabolism, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "iron metabolism disease", "shortest_name_length": 13}
{"curie": "MONDO:0007162", "names": ["ASYMMETRIC SHORT STATURE SYNDROME", "Asymmetric Short Stature Syndrome", "asymmetric short stature syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "asymmetric short stature syndrome", "shortest_name_length": 33}
{"curie": "MONDO:0018854", "names": ["acquired PF", "Acquired purpura fulminans", "acquired purpura fulminans", "Acquired purpura fulminans (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired purpura fulminans", "shortest_name_length": 11}
{"curie": "UMLS:C1334216", "names": ["Intermediate Grade Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intermediate Grade Malignant Neoplasm", "shortest_name_length": 37}
{"curie": "MONDO:0003748", "names": ["fear fly", "Aviophobia", "Aerophobia", "fear flying", "flying phobia", "phobia flying", "Flying Phobia", "Flying phobia", "Phobia, flying", "fear of flying", "Fear of flying", "Phobia of flying", "Fear (of);flying", "Flying phobia (finding)", "Fear of flying (finding)", "fear of flying (diagnosis)", "unreasonable fear of flying", "unreasonable fear of flying (symptom)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "flying phobia", "shortest_name_length": 8}
{"curie": "MONDO:0002809", "names": ["Pancreatic Cystadenoma", "Pancreatic cystadenoma", "pancreatic cystadenoma", "Cystadenoma of pancreas", "cystadenoma of pancreas", "Cystadenoma of Pancreas", "Cystadenoma of the Pancreas", "cystadenoma of the pancreas", "exocrine pancreas cystadenoma", "Cystadenoma of pancreas (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic cystadenoma", "shortest_name_length": 22}
{"curie": "MONDO:0011754", "names": ["Fhha2", "FHHA2", "hyperreninemic hypoaldosteronism, familial, 2", "Hyperreninemic Hypoaldosteronism, Familial, 2", "HYPERRENINEMIC HYPOALDOSTERONISM, FAMILIAL, 2", "familial hyperreninemic hypoaldosteronism type 2", "hyperreninemic hypoaldosteronism, familial, type 2", "aldosterone synthase deficiency unrelated to CYP11B2", "aldosterone synthase deficiency unrelated to the aldosterone synthase gene"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial hyperreninemic hypoaldosteronism type 2", "shortest_name_length": 5}
{"curie": "UMLS:C4725617", "names": ["Recurrent Endometrial Endometrioid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Endometrial Endometrioid Adenocarcinoma", "shortest_name_length": 49}
{"curie": "MONDO:0005496", "names": ["bile duct cancer", "Bile Duct Cancer", "Bile duct cancer", "bile cancer duct", "cancer bile duct", "bile duct cancers", "Bile Duct Cancers", "bile ducts cancer", "Cancer, Bile Duct", "Cancers, Bile Duct", "Bile ducts--Cancer", "Carcinoma bile duct", "CARCINOMA BILE DUCT", "BILE DUCT CARCINOMA", "Bile Duct Carcinoma", "Bile duct carcinoma", "carcinoma bile duct", "bile duct carcinoma", "Cancer of Bile Duct", "cancer of bile duct", "Bile duct cancer NOS", "carcinoma of bile duct", "CARCINOMA OF BILE DUCT", "Cancer of the Bile Duct", "cancer of the bile duct", "Bile Duct Cancer (including Cholangiocarcinoma)", "bile duct cancer (including cholangiocarcinoma)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bile duct carcinoma", "shortest_name_length": 16}
{"curie": "MONDO:0003264", "names": ["Metatypical carcinoma", "metatypical carcinoma", "basosquamous carcinoma", "CARCINOMA BASOSQUAMOUS", "Basosquamous Carcinoma", "Carcinoma basosquamous", "Basosquamous carcinoma", "Carcinoma, Basosquamous", "Basosquamous Carcinomas", "Carcinomas, Basosquamous", "basosquamous cell carcinoma", "Basisquamous cell carcinoma", "Basosquamous Cell Carcinoma", "Basi squamous cell carcinoma", "basosquamous tumor, malignant", "BASOSQUAMOUS TUMOR, MALIGNANT", "Basal squamous cell carcinoma", "basosquamous carcinoma of skin", "Basosquamous carcinoma of skin", "Carcinoma basosquamous of skin", "Metatypical basal cell carcinoma", "skin basosquamous cell carcinoma", "Skin Basosquamous Cell Carcinoma", "Mixed basal-squamous cell carcinoma", "Mixed basal - squamous cell carcinoma", "Metatypical basal cell carcinoma of skin", "Basosquamous carcinoma of skin (disorder)", "basosquamous carcinoma of skin (diagnosis)", "skin mixed basal and squamous cell carcinoma", "Skin Mixed Basal and Squamous Cell Carcinoma", "skin neoplasm malignant carcinoma basosquamous", "BCC - Metatypical basal cell carcinoma of skin", "Metatypical carcinoma (morphologic abnormality)", "metatypical carcinoma (morphologic abnormality)", "Basosquamous carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "basosquamous carcinoma", "shortest_name_length": 21}
{"curie": "MONDO:0060778", "names": ["adult Fanconi syndrome", "Adult Fanconi Syndrome", "Adult Fanconi's Syndrome", "adult Fanconi's syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult Fanconi syndrome", "shortest_name_length": 22}
{"curie": "MONDO:0002618", "names": ["malignant bone fibrous histiocytoma", "Malignant Bone Fibrous Histiocytoma", "Malignant fibrous histiocytoma of bone", "Malignant Fibrous Histiocytoma of Bone", "malignant fibrous histiocytoma of bone", "malignant fibrous histiocytoma of the bone", "malignant fibrous Histiocytoma of the bone", "Malignant Fibrous Histiocytoma of the Bone", "undifferentiated high grade pleomorphic sarcoma", "undifferentiated high-grade pleomorphic sarcoma", "Undifferentiated High-Grade Pleomorphic Sarcoma", "Undifferentiated high-grade pleomorphic sarcoma", "Undifferentiated High Grade Pleomorphic Sarcoma", "malignant fibrous histiocytoma of bone (diagnosis)", "Undifferentiated High Grade Pleomorphic Sarcoma of Bone", "undifferentiated high grade pleomorphic sarcoma of bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "undifferentiated high grade pleomorphic sarcoma of bone", "shortest_name_length": 35}
{"curie": "UMLS:C0086236", "names": ["Atonic seizure", "Atonic Epilepsy", "epilepsy atonic", "Atonic epilepsy", "Epilepsy, Atonic", "Atonic Epilepsies", "Epilepsies, Atonic", "Atonic epileptic seizure", "Atonic epilepsy (disorder)", "Atonic epilepsy (diagnosis)", "Atonic epileptic seizure (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epilepsy, Atonic", "shortest_name_length": 14}
{"curie": "MONDO:0012473", "names": ["ARPA familial", "familial ARPA", "ARPA, FAMILIAL", "ARPA, Familial", "Arpa, familial", "familial anomalous origin of right pulmonary artery", "Familial anomalous origin of right pulmonary artery", "anomalous origin of right pulmonary artery familial", "right pulmonary artery, anomalous origin of, familial", "RIGHT PULMONARY ARTERY, ANOMALOUS ORIGIN OF, FAMILIAL", "Right pulmonary artery, anomalous origin of, familial", "right pulmonary artery, anomalous origin of, with ventricular septal defect, patent Foramen ovale, and patent ductus arteriosus", "RIGHT PULMONARY ARTERY, ANOMALOUS ORIGIN OF, WITH VENTRICULAR SEPTAL DEFECT, PATENT FORAMEN OVALE, AND PATENT DUCTUS ARTERIOSUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "right pulmonary artery, anomalous origin of, familial", "shortest_name_length": 13}
{"curie": "MONDO:0015932", "names": ["isolated urogenital tract malformation of female", "nonsyndromic urogenital tract malformation of female", "non-syndromic urogenital tract malformation of female", "female organism non-syndromic urogenital tract malformation", "non-syndromic urogenital tract malformation of female organism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-syndromic urogenital tract malformation of female", "shortest_name_length": 48}
{"curie": "MONDO:0018881", "names": ["MDS", "aCML", "ACML", "MDS-U", "preleukemia", "Preleukemia", "atypical CML", "Atypical CML", "Preleukemias", "Preleukaemia", "Myelodysplasia", "MYELODYSPLASIA", "myelodysplasia", "myelodysplasias", "dysmyelopoiesis", "Dysmyelopoiesis", "Myeloid dysplasia", "Subacute myelosis", "MYELOID DYSPLASIA", "myeloid dysplasia", "subacute; myelosis", "myelosis; subacute", "Myelodysplasia NOS", "Smoldering Leukemia", "MDS, unclassifiable", "Smoldering leukemia", "smoldering leukemia", "PRELEUKEMIC SYNDROME", "Preleukemic syndrome", "syndrome; preleukemic", "Smouldering leukaemia", "preleukemic; syndrome", "Preleukaemic syndrome", "oligoblastic leukemia", "Oligoblastic Leukemia", "Myelodysplastic Neoplasm", "Myelodysplastic syndrome", "myelodysplastic syndrome", "MYELODYSPLASTIC SYNDROME", "Myelodysplastic Syndrome", "myelodysplastic neoplasm", "Dysmyelopoietic syndrome", "dysmyelopoietic syndrome", "Dysmyelopoietic Syndrome", "Subacute Myeloid Leukemia", "myelodysplastic; syndrome", "Myelodysplastic syndromes", "Subacute myeloid leukemia", "Syndrome, Dysmyelopoietic", "Syndrome, Myelodysplastic", "Myelodysplastic Syndromes", "myelodysplastic syndromes", "syndrome; myelodysplastic", "subacute myeloid leukemia", "Dysmyelopoietic Syndromes", "Syndromes, Myelodysplastic", "Subacute myeloid leukaemia", "Hypoplastic myelodysplasia", "Syndromes, Dysmyelopoietic", "myelodysplasia (diagnosis)", "Myeloid leukemia, subacute", "leukemia; myeloid, subacute", "myeloid; leukemia, subacute", "Myeloid leukaemia, subacute", "Hematopoetic Myelodysplasia", "Hematopoetic Myelodysplasias", "Myelodysplastic syndrome NOS", "Myelodysplasia, Hematopoetic", "[M]Subacute myeloid leukemia", "subacute myelogenous leukemia", "Ph1-Negative Myeloid Leukemia", "[M]Subacute myeloid leukaemia", "leukemia myelogenous subacute", "Subacute myelogenous leukemia", "Myelodysplasias, Hematopoetic", "Myelodysplastic syndrome, NOS", "Myeloid Leukemia, Ph1-Negative", "Ph1-Negative Myeloid Leukemias", "Subacute granulocytic leukemia", "Subacute myelogenous leukaemia", "MDS - Myelodysplastic syndrome", "Myeloid Leukemia, Ph1 Negative", "Leukemia, Ph1-Negative Myeloid", "Myelodysplastic syndrome (MDS)", "Subacute granulocytic leukaemia", "Leukemias, Ph1-Negative Myeloid", "Leukemia, Myeloid, Ph1-Negative", "Myeloid Leukemias, Ph1-Negative", "Leukemia, Myeloid, Ph1 Negative", "leukemia; granulocytic, subacute", "granulocytic; leukemia, subacute", "Myelodysplastic Syndrome/Neoplasm", "Ph1-Negative Myelogenous Leukemia", "defective spinal cord development", "atypical chronic myeloid leukemia", "myelodysplastic syndrome, somatic", "myelodysplastic syndrome/neoplasm", "Atypical chronic myeloid leukemia", "Atypical Chronic Myeloid Leukemia", "Atypical chronic myeloid leukaemia", "Ph1-Negative Myelogenous Leukemias", "Chronic Myeloid Leukemia, Atypical", "Myelogenous Leukemia, Ph1-Negative", "Leukemia, Ph1-Negative Myelogenous", "Myelogenous Leukemia, Ph1 Negative", "LEUKEMIA, CHRONIC MYELOID, ATYPICAL", "Myelogenous Leukemias, Ph1-Negative", "Leukemias, Ph1-Negative Myelogenous", "Leukemia, Myelogenous, Ph1 Negative", "Myelodysplastic syndrome (clinical)", "Leukemia, Myelogenous, Ph1-Negative", "Myelodysplastic syndrome (disorder)", "Subacute myeloid leukemia (disorder)", "Leukemia, Myeloid, Chronic, Atypical", "myelodysplastic syndrome (diagnosis)", "Myelodysplastic syndrome, unspecified", "Philadelphia-Negative Myeloid Leukemia", "Leukemia, Philadelphia-Negative Myeloid", "Myeloid Leukemia, Philadelphia Negative", "Myeloid Leukemia, Philadelphia-Negative", "Philadelphia-Negative Myeloid Leukemias", "Myeloid Leukemias, Philadelphia-Negative", "Leukemia, Myeloid, Philadelphia Negative", "myelodysplastic syndrome, unclassifiable", "Leukemias, Philadelphia-Negative Myeloid", "Leukemia, Myeloid, Philadelphia-Negative", "subacute myelogenous leukemia (diagnosis)", "Philadelphia-Negative Myelogenous Leukemia", "MYELODYSPLASTIC SYNDROME, SUSCEPTIBILITY TO", "myelodysplastic syndrome, susceptibility to", "Atypical chronic myeloid leukemia (disorder)", "Atypical chronic myeloid leukemia (diagnosis)", "hematopoeitic - myelodysplastic syndrome (MDS)", "Hematopoeitic - Myelodysplastic Syndrome (MDS)", "Myelodysplastic syndrome (morphologic abnormality)", "Subacute myeloid leukemia (morphologic abnormality)", "Atypical chronic myeloid leukemia, BCR/ABL-negative", "Atypical chronic myeloid leukemia, BCR/ABL negative", "Atypical chronic myeloid leukaemia, BCR/ABL negative", "atypical chronic myeloid leukemia, BCR-ABL1 negative", "Atypical Chronic Myeloid Leukemia, BCR-ABL1 Negative", "Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative", "Subacute myeloid leukemia without mention of remission", "Subacute myeloid leukaemia without mention of remission", "Subacute myeloid leukemia, without mention of remission", "Atypical chronic myeloid leukemia, BCR/ABL-negative NOS", "Subacute myeloid leukaemia, without mention of remission", "Atypical chronic myeloid leukemia, Philadelphia chromosome (Ph1) negative", "Atypical chronic myeloid leukaemia, Philadelphia chromosome (Ph1) negative", "Atypical chronic myeloid leukemia, BCR/ABL negative (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myelodysplastic syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C0155219", "names": ["Eyelid vascular disorder", "Eyelid Vascular Disorder", "Vascular anomaly of eyelid", "vascular anomalies of eyelid", "Eyelid vascular disorder NOS", "Vascular anomalies of eyelid", "eyelid disorder vascular anomaly", "Vascular anomaly of eyelid (disorder)", "Vascular anomaly of eyelid (diagnosis)", "vascular anomalies of eyelid (diagnosis)", "vascular anomalies of eyelid (physical finding)", "Vascular anomalies of unspecified eye, unspecified eyelid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vascular anomaly of eyelid", "shortest_name_length": 24}
{"curie": "UMLS:C0339174", "names": ["conjunctiva; injury", "Conjunctival injury", "Conjunctival Injury", "injury; conjunctiva", "conjunctival injury", "Injury of conjunctiva", "Conjunctival injuries", "conjunctival injury (diagnosis)", "Injury of conjunctiva (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of conjunctiva", "shortest_name_length": 19}
{"curie": "UMLS:C0271190", "names": ["Polyopia", "polyopia", "diplopia monocular", "Monocular Diplopia", "Uniocular diplopia", "monocular diplopia", "Monocular diplopia", "unilateral diplopia", "Monocular Diplopias", "Diplopia, Monocular", "Unilateral Diplopia", "Diplopia, Unilateral", "Diplopias, Monocular", "Unilateral Diplopias", "DIPLOPIA, UNILATERAL", "Diplopias, Unilateral", "double vision one eye", "double vision in one eye", "Double vision in one eye", "unilateral diplopia (symptom)", "Monocular diplopia (disorder)", "monocular diplopia (diagnosis)", "seeing double images in one eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diplopia, Unilateral", "shortest_name_length": 8}
{"curie": "MONDO:0012252", "names": ["RTPS1", "At/RT", "Atypical teratoid tumors", "Teratoid Tumor, Atypical", "TERATOID TUMOR, ATYPICAL", "teratoid tumor, atypical", "rhabdoid tumors, somatic", "SMARCB1 familial rhabdoid tumor", "malignant rhabdoid tumor, somatic", "MALIGNANT RHABDOID TUMOR, SOMATIC", "Malignant Rhabdoid Tumor, Somatic", "rhabdoid tumor predisposition syndrome 1", "RHABDOID TUMOR PREDISPOSITION SYNDROME 1", "Rhabdoid Tumor Predisposition Syndrome 1", "rhabdoid tumor predisposition syndrome type 1", "brain tumor, posterior fossa, of infancy, familial", "BRAIN TUMOR, POSTERIOR FOSSA, OF INFANCY, FAMILIAL", "Brain Tumor, Posterior Fossa, of Infancy, Familial", "RHABDOID TUMOR PREDISPOSITION SYNDROME 1 (disorder)", "familial rhabdoid tumor caused by mutation in SMARCB1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rhabdoid tumor predisposition syndrome 1", "shortest_name_length": 5}
{"curie": "UMLS:C0080107", "names": ["Respiratory Tract Fistula", "Respiratory Tract Fistulas", "Fistula, Respiratory Tract", "Respiratory System Fistula", "Fistula, Respiratory System", "Respiratory System Fistulas", "Fistulas, Respiratory Tract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Respiratory Tract Fistula", "shortest_name_length": 25}
{"curie": "MONDO:0000952", "names": ["hindlimb long bone cancer", "cancer of hindlimb long bone", "long bones of lower limb cancer", "cancer of long bone of lower limb", "malignant hindlimb long bone neoplasm", "malignant neoplasm of long bones of leg", "malignant neoplasm of hindlimb long bone", "Malignant neoplasm of long bone of lower limb", "Malignant neoplasm of long bones of lower limb", "malignant neoplasm of long bones of lower limbs", "Malignant neoplasm of long bone of lower limb, NOS", "Malignant neoplasm of long bone of lower limb (disorder)", "malignant neoplasm of long bones of lower limbs (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cancer of long bone of lower limb", "shortest_name_length": 25}
{"curie": "MONDO:0017890", "names": ["Tubulocystic renal cell cancer", "Tubulocystic Renal Cell Cancer", "tubulocystic renal cell carcinoma", "Tubulocystic Renal Cell Carcinoma", "Tubulocystic renal cell carcinoma", "Tubulocystic renal cell carcinoma (disorder)", "Tubulocystic renal cell carcinoma (diagnosis)", "Tubulocystic renal cell carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tubulocystic renal cell carcinoma", "shortest_name_length": 30}
{"curie": "UMLS:C4331311", "names": ["Stage 0 Major Salivary Gland Cancer", "Stage 0 Major Salivary Gland Cancer AJCC v8", "Stage 0 Major Salivary Gland Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Major Salivary Gland Cancer AJCC v8", "shortest_name_length": 35}
{"curie": "MONDO:0012064", "names": ["OOFD", "BMKS", "Burn McKeown syndrome", "Burn-McKeown syndrome", "Burn-Mckeown syndrome", "BURN-MCKEOWN SYNDROME", "Oculootofacial Dysplasia", "oculootofacial dysplasia", "OCULOOTOFACIAL DYSPLASIA", "choanal atresia deafness cardiac defects dysmorphism", "Choanal atresia - deafness - cardiac defects - dysmorphism syndrome", "choanal atresia-hearing loss-cardiac defects-craniofacial dysmorphism syndrome", "Choanal atresia-hearing loss-cardiac defects-craniofacial dysmorphism syndrome", "Bilateral choanal atresia, cardiac defects, deafness, and dysmorphic appearance", "bilateral choanal atresia, cardiac defects, deafness, and dysmorphic appearance", "Choanal atresia, hearing loss, cardiac defect, craniofacial dysmorphism syndrome", "Choanal atresia, hearing loss, cardiac defect, craniofacial dysmorphism syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choanal atresia-hearing loss-cardiac defects-craniofacial dysmorphism syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C1332942", "names": ["Anaplastic Large Cell Lymphoma", "Pediatric Anaplastic Large Cell Lymphoma", "Childhood Anaplastic Large Cell Lymphoma", "childhood anaplastic large cell lymphoma", "Pediatric K-1+ Anaplastic Large Cell Lymphoma", "Childhood K-1+ Anaplastic Large Cell Lymphoma", "Childhood CD30+ Anaplastic Large Cell Lymphoma", "Pediatric CD30+ Anaplastic Large Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Anaplastic Large Cell Lymphoma", "shortest_name_length": 30}
{"curie": "MONDO:0003147", "names": ["Outerspace sickness", "Outer space sickness", "space motion sickness", "Space Motion Sickness", "Motion Sickness, Space", "motion sickness, Space", "Space Adaptation Syndrome", "space adaptation syndrome", "Space adaptation syndrome", "syndrome, Space adaptation", "adaptation syndrome, Space", "Adaptation Syndrome, Space", "Syndrome, Space Adaptation", "Outer space sickness (finding)", "space adaptation syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "space motion sickness", "shortest_name_length": 19}
{"curie": "UMLS:C0850638", "names": ["infected bite", "bite infected", "Infected bite", "Infection;bite", "infected bites", "bites infected", "Infected bites", "bite infection", "bite infections", "biting infection", "biting infections"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infected bite", "shortest_name_length": 13}
{"curie": "MONDO:8000012", "names": ["IMNEPD", "IMNEPD1", "Infantile multisystem neurologic-endocrine-pancreatic disease", "infantile-onset multisystem neurologic, endocrine, and pancreatic disease", "neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset", "NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET 1", "neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 1", "shortest_name_length": 6}
{"curie": "MONDO:0024890", "names": ["Pinealoma", "pinealoma", "Pinealomas", "pineal tumor", "Pineal tumor", "Pineal Tumor", "Pineal Tumors", "pineal tumors", "Tumor, Pineal", "Pineal tumour", "Tumors, Pineal", "Pineal neoplasm", "Pineal Neoplasm", "pineocytic tumor", "Neoplasm, Pineal", "Pineocytic Tumor", "benign pinealoma", "Pineal Neoplasms", "Neoplasms, Pineal", "Pineal Gland Tumor", "pineal gland tumor", "gland pineal tumor", "gland pineal tumors", "Pineal neoplasm NOS", "Tumor, Pineal Gland", "pineal gland tumour", "pineal region tumor", "Pineocytic Neoplasm", "pineocytic neoplasm", "PINEAL GLAND, TUMOR", "Pineal Gland Tumors", "pineal body neoplasm", "Pineal gland--Tumors", "pineal region tumors", "gland pineal tumours", "Tumors, Pineal Gland", "Pinealoma (disorder)", "Tumor of Pineal Gland", "pineal gland neoplasm", "Tumor of pineal gland", "Pineal Gland Neoplasm", "pinealoma (diagnosis)", "tumor of pineal gland", "Tumour of pineal gland", "Neoplasm of Pineal Gland", "Pineal parenchymal tumor", "pineal parenchymal tumor", "Pineal Parenchymal Tumor", "Neoplasm of pineal gland", "neoplasm of pineal gland", "Tumor, Pineal Parenchymal", "tumor of the pineal gland", "Pineal parenchymal tumour", "BRAIN TUMOR, PINEAL GLAND", "Tumor of the Pineal Gland", "Pineal Parenchymal Tumors", "Tumors, Pineal Parenchymal", "pineal parenchymal neoplasm", "Pineal Parenchymal Neoplasm", "Neoplasm of the Pineal Gland", "neoplasm of the pineal gland", "benign pinealoma (diagnosis)", "pineal parenchymal cell tumor", "Pineal Parenchymal Cell Tumor", "pineal parenchymal cell neoplasm", "Pineal parenchymal cell neoplasm", "Pineal Parenchymal Cell Neoplasm", "neoplasm of endocrine gland pineal", "Neoplasm of pineal gland (disorder)", "INTRACRANIAL NEOPLASM, PINEAL GLAND", "Neoplasm of pineal gland (diagnosis)", "neoplasm uncertain behavior pinealoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pineal parenchymal cell neoplasm", "shortest_name_length": 9}
{"curie": "MONDO:0004947", "names": ["B-ALL", "b all", "c-ALL", "pre-b", "b-all", "c all", "pro b", "FAB L3", "Pre-B ALL", "Pro-B ALL", "Common ALL", "B-Cell ALL", "Pre-pre-B ALL", "Burkitt Leukemia", "burkitt leukemia", "Leukemia, Burkitt", "burkitts leukemia", "Burkitts Leukemia", "burkitt's leukemia", "Burkitt's Leukemia", "Burkitt's leukemia", "Leukemia, Burkitt's", "Burkitt's leukaemia", "leukemia Burkitt cell", "Burkitt Cell Leukemia", "Burkitt cell leukemia", "Leukemia, Burkitt Cell", "cell leukemia; Burkitt", "Burkitt cell leukaemia", "Burkitt; cell leukemia", "Common precursor B ALL", "Burkitt's Cell Leukemia", "Burkitt's cell leukemia", "L3 Lymphocytic Leukemia", "Burkitt's cell leukaemia", "L3 Lymphocytic Leukemias", "Lymphocytic Leukemia, L3", "Leukemia, L3 Lymphocytic", "Leukemia, Lymphocytic, L3", "Burkitt lymphoma/leukemia", "B-cell type acute leukemia", "L3 Acute Lymphoid Leukemia", "B-Cell Type Acute Leukemia", "B-cell type acute leukaemia", "L3 Acute Lymphocytic Leukemia", "B-Cell Lymphoblastic Leukemia", "B-Acute Lymphoblastic Leukemia", "B-cell type acute leukemia NOS", "B Acute Lymphoblastic Leukemia", "L3 Acute Lymphogenous Leukemia", "L3 Acute Lymphoblastic Leukemia", "B-cell type acute leukaemia NOS", "B-lymphoblastic leukemia/lymphoma", "B lymphoblastic leukemia/lymphoma", "B Lymphoblastic Leukemia/Lymphoma", "B-Lymphoblastic Leukemia/Lymphoma", "B-cell acute lymphocytic leukemia", "B lymphoblastic leukemia lymphoma", "Burkitt cell leukemia (diagnosis)", "Precursor B-Lymphoblastic Leukemia", "B lymphoblastic leukaemia lymphoma", "B-Cell Acute Lymphoblastic Leukemia", "Mature B-cell leukemia Burkitt-type", "B-cell acute lymphoblastic leukemia", "Mature B-cell leukemia Burkitt type", "Mature B-cell leukaemia Burkitt type", "B-Cell Precursor Type Acute Leukemia", "B-cell acute lymphoblastic leukaemia", "Mature B-cell leukaemia Burkitt-type", "B Cell Precursor Type Acute Leukemia", "Leukemia, Lymphoblastic, Burkitt-Type", "B-Cell Lymphoblastic Leukemia/Lymphoma", "precursor B-cell lymphoblastic leukemia", "precursor b-cell lymphoblastic leukemia", "Precursor B-cell lymphoblastic leukemia", "Mature B-cell leukemia Burkitt-type NOS", "Precursor B-cell lymphoblastic leukaemia", "Precursor B Lymphoblastic Leukemia/Lymphoma", "precursor B lymphoblastic lymphoma/leukemia", "Precursor B-Lymphoblastic Lymphoma/Leukemia", "precursor B-lymphoblastic lymphoma/leukemia", "precursor B lymphoblastic leukemia/lymphoma", "Precursor B-lymphoblastic lymphoma/leukemia", "Acute lymphoblastic leukemia, Burkitt's type", "Precursor B-lymphoblastic lymphoma/leukaemia", "Burkitt; acute lymphoblastic leukemia (type)", "leukemia precursor cell lymphoblastic B-cell", "Acute lymphoblastic leukaemia, Burkitt's type", "B-cell acute lymphocytic leukemia (diagnosis)", "B lymphoblastic leukemia lymphoma (diagnosis)", "B-cell acute lymphoblastic leukemia (disorder)", "Burkitt cell leukemia (morphologic abnormality)", "Acute lymphoblastic leukemia, mature B-cell type", "Acute lymphoblastic leukaemia, mature B-cell type", "precursor B-cell lymphoblastic leukemia (diagnosis)", "B lymphoblastic leukemia lymphoma (morphologic abnormality)", "malignant neoplasm primary B lymphoblastic leukemia lymphoma", "Precursor B-cell lymphoblastic leukemia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-cell acute lymphoblastic leukemia", "shortest_name_length": 5}
{"curie": "MONDO:0013200", "names": ["CMH15", "hypertrophic cardiomyopathy 15", "VCL hypertrophic cardiomyopathy", "cardiomyopathy, hypertrophic, 15", "hypertrophic cardiomyopathy type 15", "cardiomyopathy familial hypertrophic 15", "Cardiomyopathy, Familial Hypertrophic, 15", "cardiomyopathy, familial hypertrophic, 15", "CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 15", "cardiomyopathy, familial hypertrophic, type 15", "hypertrophic cardiomyopathy caused by mutation in VCL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophic cardiomyopathy 15", "shortest_name_length": 5}
{"curie": "UMLS:C0156689", "names": ["Unspecified Antepartum Hypertension", "Unspecified antepartum hypertension", "Unspecified hypertension complicating pregnancy, childbirth, or the puerperium, antepartum condition or complication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unspecified antepartum hypertension", "shortest_name_length": 35}
{"curie": "UMLS:C1997322", "names": ["Chlamydia trachomatis genital infection", "Chlamydia trachomatis infection of genital structure", "STD due to Chlamydia trachomatis of genital structure", "STD of genital structure due to Chlamydia trachomatis", "Chlamydia trachomatis infection of genital structure (disorder)", "STD of genital structure due to Chlamydia trachomatis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chlamydia trachomatis infection of genital structure", "shortest_name_length": 39}
{"curie": "MONDO:0019762", "names": ["LTEC2", "LTEC II", "laryngotracheoesophageal cleft type 2", "laryngo-tracheo-esophageal cleft type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laryngotracheoesophageal cleft type 2", "shortest_name_length": 5}
{"curie": "UMLS:C0796618", "names": ["stage IB soft tissue sarcoma", "Stage IB Soft Tissue Sarcoma", "stage IB sarcoma of soft tissue", "Stage IB Sarcoma of Soft Tissue", "stage IB adult soft tissue sarcoma", "Stage IB Sarcoma of the Soft Tissue", "stage IB sarcoma of the soft tissue", "Stage IB Soft Tissue Sarcoma AJCC v7", "stage IB soft tissue sarcoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Soft Tissue Sarcoma AJCC v7", "shortest_name_length": 28}
{"curie": "MONDO:0037858", "names": ["disorder of fat oxidation", "Disorder of fat oxidation", "fatty acid metabolism disorder", "metabolic disorder; fatty acid", "fatty acid; metabolic disorder", "Fatty Acid Metabolism Disorder", "disorder of fatty acid metabolism", "Disorder of fatty acid metabolism", "Disorders of fatty-acid metabolism", "disorders of fatty-acid metabolism", "DISORDERS OF FATTY ACID METABOLISM", "Disorder of fatty acid metabolism, NOS", "inherited fatty acid metabolism disorder", "Disorder of fatty acid metabolism (disorder)", "disorder of fatty acid metabolism (diagnosis)", "Disorder of fatty-acid metabolism, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited fatty acid metabolism disorder", "shortest_name_length": 25}
{"curie": "MONDO:0054765", "names": ["ACD", "PLCA3", "Amyloidosis cutis dyschromia", "amyloidosis cutis dyschromica", "Amyloidosis cutis dyschromica", "AMYLOIDOSIS CUTIS DYSCHROMICA", "Amyloidosis cutis dyschromia (disorder)", "Amyloidosis cutis dyschromia (diagnosis)", "AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 3", "amyloidosis, PRIMARY LOCALIZED cutaneous, 3", "amyloidosis, primary localized cutaneous, 3", "amyloidosis skin primary localized cutis dyschromia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyloidosis, primary localized cutaneous, 3", "shortest_name_length": 3}
{"curie": "MONDO:0017184", "names": ["autosomal dominant hyperinsulinism due to SUR1 deficiency", "Autosomal dominant hyperinsulinism due to SUR1 deficiency", "Autosomal dominant hyperinsulinemic hypoglycemia due to SUR1 deficiency", "autosomal dominant hyperinsulinemic hypoglycemia due to SUR1 deficiency", "Autosomal dominant hyperinsulinism due to sulfonylurea receptor 1 deficiency", "Autosomal dominant hyperinsulinism due to sulfonylurea receptor 1 deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant hyperinsulinism due to SUR1 deficiency", "shortest_name_length": 57}
{"curie": "MONDO:0002451", "names": ["prostate phyllodes tumor", "prostate phyllodes tumour", "benign prostate phyllodes tumor", "Benign Prostate Phyllodes Tumor", "prostate phyllodes tumor, benign", "benign prostate phyllodes tumour", "Benign Prostate Phyllodes Neoplasm", "Benign Phyllodes Tumor of Prostate", "benign prostate phyllodes neoplasm", "Phyllodes neoplasm of the prostate", "benign phyllodes tumor of prostate", "phyllodes neoplasm of the prostate", "benign phyllodes neoplasm of prostate", "Benign Phyllodes Neoplasm of Prostate", "Benign Phyllodes Tumor of the Prostate", "benign phyllodes tumor of the prostate", "benign phyllodes neoplasm of the prostate", "benign Phyllodes neoplasm of the prostate", "Benign Phyllodes Neoplasm of the Prostate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign prostate phyllodes tumor", "shortest_name_length": 24}
{"curie": "MONDO:0016422", "names": ["PAS3", "APS3", "APS type 3", "autoimmune polyendocrinopathy type 3", "Autoimmune polyendocrinopathy type 3", "Autoimmune polyendocrine syndrome type 3", "polyglandular autoimmune syndrome type 3", "autoimmune polyglandular syndrome type 3", "Autoimmune polyglandular syndrome type 3", "autoimmune polyendocrine syndrome type 3", "Autoimmune Polyglandular Syndrome, Type 3", "Polyglandular Autoimmune Syndrome, Type 3", "Polyglandular Type III Autoimmune Syndrome", "Polyglandular autoimmune syndrome type III", "autoimmune polyendocrine syndrome type III", "Autoimmune Polyglandular Syndrome Type III", "Autoimmune Syndrome Type III, Polyglandular", "Autoimmune polyendocrine syndrome type 3 (disorder)", "autoimmune polyendocrine syndrome type III (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune polyendocrinopathy type 3", "shortest_name_length": 4}
{"curie": "MONDO:0006615", "names": ["Sweat gland disease", "Sweat Gland Disease", "sweat gland disease", "Sweat gland disorder", "SWEAT GLAND DISORDER", "sweat gland disorder", "Disease, Sweat Gland", "Sweat Gland Diseases", "Sweat Gland Disorders", "Diseases, Sweat Gland", "sweat gland disorders", "diseases glands sweat", "sweat gland(s) disease", "disease of sweat gland", "Sweat glands--Diseases", "sweat glands disorders", "Disease;sweat gland(s)", "SWEAT GLAND ABNORMALITY", "disorder of sweat gland", "Eccrine sweat disorders", "Disease of sweat glands", "disease of sweat glands", "Disorder of sweat gland", "Sweat gland disorder NOS", "Disorder of sweat glands", "disorder of sweat glands", "Abnormalities of sweating", "Disorders of sweat glands", "DISEASES OF THE SWEAT GLANDS", "Disease of sweat glands, NOS", "Disorder of sweat glands NOS", "Disorder of sweat glands, NOS", "Abnormality of the sweat gland", "Abnormal sweat gland morphology", "sweat gland disease or disorder", "disease (or disorder); sweat gland", "disease or disorder of sweat gland", "Disorder of sweat gland (disorder)", "disorder of sweat gland (diagnosis)", "Eccrine sweat disorder, unspecified", "Unspecified disorder of sweat glands"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sweat gland disorder", "shortest_name_length": 19}
{"curie": "MONDO:0015592", "names": ["Limbic encephalitis with LGI1 antibodies", "limbic encephalitis with LGI1 antibodies", "Limbic encephalitis with leucine-rich glioma-inactivated 1 antibodies", "encephalitis limbic with leucine-rich glioma-inactivated 1 antibodies", "limbic encephalitis with leucine-rich glioma-inactivated 1 antibodies", "Limbic encephalitis with leucine-rich glioma-inactivated 1 antibodies (disorder)", "Limbic encephalitis with leucine-rich glioma-inactivated 1 antibodies (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "limbic encephalitis with LGI1 antibodies", "shortest_name_length": 40}
{"curie": "MONDO:0007077", "names": ["TADS", "Tietz syndrome", "TIETZ SYNDROME", "Tietz's syndrome", "Albinism-deafness of Tietz", "ALBINISM-DEAFNESS OF TIETZ", "albinism-deafness of Tietz", "Tietz albinism-deafness syndrome", "TIETZ ALBINISM-DEAFNESS SYNDROME", "Hypopigmentation-deafness syndrome", "Hypopigmentation-deafness of Tietz", "HYPOPIGMENTATION/DEAFNESS OF TIETZ", "hypopigmentation-deafness syndrome", "hypopigmentation/deafness of Tietz", "Generalized piebaldism and deafness", "Albinism-deafness syndrome of Tietz", "Albinism and complete nerve deafness", "Hypopigmentation-hearing loss syndrome", "Albinism-deafness syndrome of Tietz (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tietz syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0010509", "names": ["MRX104", "XLID104", "X-linked mental retardation 104", "mental retardation, X-linked 104", "MENTAL RETARDATION, X-LINKED 104", "intellectual disability, X-linked 104", "mental retardation, X-linked type 104", "intellectual disability, X-linked type 104", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 104", "intellectual developmental disorder, X-linked 104", "non-syndromic X-linked intellectual disability 104", "FRMPD4 non-syndromic X-linked intellectual disability", "non-syndromic X-linked intellectual disability caused by mutation in FRMPD4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 104", "shortest_name_length": 6}
{"curie": "MONDO:0002367", "names": ["renal cancer", "Renal Cancer", "Renal cancer", "Kidney Cancer", "Kidney cancer", "Renal Cancers", "Cancer, Renal", "renal cancers", "KIDNEY CANCER", "kidney cancer", "Cancers, Renal", "kidney cancers", "Kidney Cancers", "Cancer, Kidney", "Kidneys--Cancer", "Cancers, Kidney", "Kidney Neoplasms", "cancer of kidney", "Cancer of Kidney", "CA - Renal cancer", "renal cell cancer", "cancer of the kidney", "Cancer of the Kidney", "CA - Cancer of kidney", "Malignant Renal Tumor", "malignant renal tumor", "Neoplasm malig;kidney", "Renal malignant tumor", "malignant renal tumors", "Renal malignant tumour", "malignant kidney tumor", "Malignant Kidney Tumor", "Renal malignant neoplasm", "Malignant Renal Neoplasm", "malignant renal neoplasm", "Malignant renal neoplasm", "Malignant Kidney Neoplasm", "Malignant Tumor of Kidney", "malignant tumor of kidney", "Malignant tumor of kidney", "malignant kidney neoplasm", "kidney cancer (diagnosis)", "Renal neoplasms malignant", "Kidney (renal cell) cancer", "malignant tumour of kidney", "Malignant tumour of kidney", "Malignant Neoplasm of Kidney", "Malignant neoplasm of kidney", "malignant neoplasm of kidney", "malignant tumor of the kidney", "Malignant Tumor of the Kidney", "malignant neoplasm of the kidney", "Malignant Neoplasm of the Kidney", "Malignant neoplasm of kidney NOS", "Malignant neoplasm of kidney, NOS", "malignant neosplasm of the kidney", "Malignant tumor of kidney (disorder)", "Malignant Kidney Neoplasm Except Pelvis", "malignant neoplasm of kidney (diagnosis)", "Malignant neoplasm of kidney, excl pelvis", "Malignant Neoplasm of Kidney Except Pelvis", "malignant neoplasm of kidney except pelvis", "Malignant neoplasm of kidney, except pelvis", "Malignant neoplasm of kidney, excluding pelvis", "Malignant neoplasm of kidney, except renal pelvis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kidney cancer", "shortest_name_length": 12}
{"curie": "MONDO:0004062", "names": ["mixed cell type uveal melanoma", "mixed cell type Uveal melanoma", "intraocular mixed cell type melanoma", "Intermediate cell type uveal melanoma", "Intermediate Cell Type Uveal Melanoma", "intermediate cell type uveal melanoma", "Uveal Intermediate Cell Type Melanoma", "Intermediate Cell Type Intraocular Melanoma", "Intermediate cell type intraocular melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intermediate cell type uveal melanoma", "shortest_name_length": 30}
{"curie": "UMLS:C5557251", "names": ["Vaso-Occlusive Crisis of Hemoglobin SS Disease", "Vaso-Occlusive Crisis in Hemoglobin SS Disease", "Vaso-Occlusive Crisis of Sickle Cell-SS Disease", "Vaso-Occlusive Crisis in Sickle Cell-SS Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaso-Occlusive Crisis in Sickle Cell-SS Disease", "shortest_name_length": 46}
{"curie": "MONDO:0018697", "names": ["Del(1)(p35.2)", "monosomy 1p35.2", "deletion 1p35.2", "1p35.2 microdeletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "1p35.2 microdeletion syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0060766", "names": ["Anal Polyp", "Anal polyp", "ANAL POLYP", "anal polyp", "anal polyps", "polyp; anus", "anus; polyp", "polyp of anus", "Polyp of Anus", "Polyp of the Anus", "polyp of the anus", "Anal polyp (disorder)", "anal polyps (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anal polyp", "shortest_name_length": 10}
{"curie": "UMLS:C5238795", "names": ["Mitochondrial", "Muscular Dystrophy Secondary to Mitochondrial Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Muscular Dystrophy Secondary to Mitochondrial Disorder", "shortest_name_length": 13}
{"curie": "MONDO:0019037", "names": ["PSP", "PSP syndrome", "Richardson Syndrome", "Richardson syndrome", "Classic PSP syndrome", "Richardson's Syndrome", "Steele-Richardson-Olszewski", "SUPRANUCLEAR PALSY PROGRESSIVE", "palsy progressive supranuclear", "supranuclear progressive palsy", "progressive supranuclear palsy", "Progressive supranuclear palsy", "Progressive Supranuclear Palsy", "Palsy, Progressive Supranuclear", "supranuclear palsy, progressive", "Supranuclear Palsy, Progressive", "Progressive Supranuclear Palsies", "PALSY, SUPRANUCLEAR, PROGRESSIVE", "Heterogeneous system degeneration", "NUCHAL DYSTONIA DEMENTIA SYNDROME", "Supranuclear Palsies, Progressive", "Nuchal dystonia-dementia syndrome", "Steele-Richardson-Olszewski disease", "Steele-Richardson-Olszewski Disease", "Steele Richardson Olszewski Disease", "PSP - Progressive supranuclear palsy", "STEELE-RICHARDSON-OLSZEWSKI SYNDROME", "Steele-Richardson-Olszewski syndrome", "Richardson-Steele-Olszewski syndrome", "Steele-Richardson-Olszewski Syndrome", "PSP - progressive supranuclear palsy", "Steele Richardson Olszewski Syndrome", "Progressive supranuclear ophthalmoplegia", "progressive supranuclear ophthalmoplegia", "Progressive supranuclear palsy (disorder)", "progressive supranuclear palsy (diagnosis)", "familial progressive supranuclear palsy (type)", "Classic progressive supranuclear palsy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive supranuclear palsy", "shortest_name_length": 3}
{"curie": "MONDO:0005398", "names": ["UADT Neoplasm", "UADT Neoplasms", "Neoplasm, UADT", "Neoplasms, UADT", "Upper Aerodigestive Tract Neoplasm", "upper aerodigestive tract neoplasm", "Upper Aerodigestive Tract Neoplasms", "Neoplasms, Upper Aerodigestive Tract", "Neoplasm of upper aerodigestive tract", "Neoplasm of upper aerodigestive tract (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "upper aerodigestive tract neoplasm", "shortest_name_length": 13}
{"curie": "UMLS:C5207031", "names": ["VAHS", "IAHS", "Virus-associated hemophagocytic syndrome", "Virus-Associated Hemophagocytic Syndrome", "Hemophagocytic syndrome associated with an infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Virus-Associated Hemophagocytic Syndrome", "shortest_name_length": 4}
{"curie": "MONDO:8000005", "names": ["fungal discitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fungal discitis", "shortest_name_length": 15}
{"curie": "MONDO:0001120", "names": ["Chronic Frontal Sinusitis", "chronic frontal sinusitis", "Chronic frontal sinusitis", "frontal sinusitis, chronic", "Chronic frontal sinusitis (disorder)", "chronic frontal sinusitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic frontal sinusitis", "shortest_name_length": 25}
{"curie": "UMLS:C1456863", "names": ["Vasoconstriction", "Pathologic vasoconstriction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic vasoconstriction", "shortest_name_length": 16}
{"curie": "UMLS:C5203866", "names": ["Prostate Adenocarcinoma with Paneth Cell-Like Neuroendocrine Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Adenocarcinoma with Paneth Cell-Like Neuroendocrine Differentiation", "shortest_name_length": 76}
{"curie": "MONDO:0001805", "names": ["female breast central part cancer", "Malignant neoplasm of central part of female breast", "malignant neoplasm of central part of female breast", "malignant tumor of central portion of female breast", "malignant neoplasm of central portion of female breast", "Malignant neoplasm of central portion of female breast", "Malignant neoplasm of central portion of breast, female", "Malignant neoplasm of central part of female breast (disorder)", "malignant neoplasm of central portion of female breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "female breast central part cancer", "shortest_name_length": 33}
{"curie": "MONDO:0000437", "names": ["ataxia", "Ataxia", "rare ataxia", "ataxia syndrome", "ataxia cerebellar", "Cerebellar ataxia", "ATAXIA CEREBELLAR", "cerebellar ataxia", "CEREBELLAR ATAXIA", "Ataxia cerebellar", "Cerebellar Ataxia", "cerebellar; ataxia", "ataxia, cerebellar", "Ataxia, cerebellar", "cerebellar Ataxias", "ataxia; cerebellar", "Ataxia, Cerebellar", "cerebellar ataxias", "Cerebellar Ataxias", "Ataxias, Cerebellar", "ataxias, cerebellar", "cerebellar dysmetria", "cerebellar Dysmetrias", "Cerebellar ataxia NOS", "Spinocerebellar ataxia", "Spinocerebellar Ataxia", "Cerebellar ataxia, NOS", "spinocerebellar ataxia", "Spinocerebellar Atrophy", "Spinocerebellar atrophy", "Ataxia, Spinocerebellar", "Spinocerebellar Ataxias", "ATAXIA, SPINOCEREBELLAR", "ataxia; spinocerebellar", "spinocerebellar; ataxia", "spinocerebellar atrophy", "spinocerebellar ataxias", "Ataxias, Spinocerebellar", "Atrophy, Spinocerebellar", "Cerebellar Incoordination", "Spinocerebellar Atrophies", "Cerebellar Incoordinations", "Atrophies, Spinocerebellar", "Incoordination, Cerebellar", "Incoordinations, Cerebellar", "Spinocerebellar Degeneration", "spinocerebellar Degeneration", "Cerebellar ataxia (disorder)", "cerebellar ataxia (diagnosis)", "Spinocerebellar ataxia (disorder)", "Cerebellar ataxia (loss of muscle coordination)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellar ataxia", "shortest_name_length": 6}
{"curie": "UMLS:C1334826", "names": ["Multiple Pyogenic Granulomas", "Multiple Lobular Capillary Hemangiomas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Multiple Lobular Capillary Hemangiomas", "shortest_name_length": 28}
{"curie": "UMLS:C2348664", "names": ["testicular choriocarcinoma and yolk sac tumor", "yolk sac tumor and choriocarcinoma, testicular", "choriocarcinoma and yolk sac tumor of the testis", "testis cancer, yolk sac tumor and choriocarcinoma", "testis cancer, choriocarcinoma and yolk sac tumor", "testicle cancer, choriocarcinoma and yolk sac tumor", "Testicular Mixed Choriocarcinoma and Yolk Sac Tumor", "testicular cancer, choriocarcinoma and yolk sac tumor", "testicular cancer, yolk sac tumor and choriocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular Mixed Choriocarcinoma and Yolk Sac Tumor", "shortest_name_length": 45}
{"curie": "MONDO:0011474", "names": ["PFHB1B", "Pfhbib", "PFHBIB", "TRPM4 progressive familial heart block", "progressive familial heart block type IB", "heart block progressive familial type 1B", "progressive familial heart block type 1B", "progressive familial heart block, type IB", "progressive familial heart block, type 1B", "PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IB", "Progressive familial heart block, type IB", "Progressive Familial Heart Block, Type Ib", "Progressive familial heart block, type IB (disorder)", "progressive familial heart block caused by mutation in TRPM4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive familial heart block type IB", "shortest_name_length": 6}
{"curie": "UMLS:C4721655", "names": ["Stage III Ovarian Dysgerminoma", "Stage III Ovarian Dysgerminoma AJCC v7", "Stage III Ovarian Dysgerminoma AJCC v6", "Stage III Ovarian Dysgerminoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Ovarian Dysgerminoma AJCC v6 and v7", "shortest_name_length": 30}
{"curie": "UMLS:C0749394", "names": ["HIV-Related Thrombocytopenia", "THROMBOCYTOPENIA HIV RELATED", "AIDS-Related Thrombocytopenia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HIV-Related Thrombocytopenia", "shortest_name_length": 28}
{"curie": "MONDO:0054708", "names": ["RP80", "retinitis pigmentosa 80", "RETINITIS PIGMENTOSA 80", "RETINITIS pigmentosa 80"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 80", "shortest_name_length": 4}
{"curie": "MONDO:0700123", "names": ["SMARCC1-related BAFopathy", "SMARCC1-associated developmental dysgenesis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SMARCC1-associated developmental dysgenesis syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0020637", "names": ["Mendelian susceptibility to mycobacterial diseases due to a partial deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mendelian susceptibility to mycobacterial diseases due to a partial deficiency", "shortest_name_length": 78}
{"curie": "MONDO:0020343", "names": ["alpha-crystallinopathy", "CRYAB-related myofobrillar myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alpha-crystallinopathy", "shortest_name_length": 22}
{"curie": "UMLS:C3146263", "names": ["Stage I Prostate Cancer", "Stage I Prostate Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Prostate Cancer AJCC v7", "shortest_name_length": 23}
{"curie": "MONDO:0012653", "names": ["PHPVAD", "Persistent Hyperplastic Primary Vitreous, Autosomal Dominant", "persistent hyperplastic primary vitreous, autosomal dominant", "PERSISTENT HYPERPLASTIC PRIMARY VITREOUS, AUTOSOMAL DOMINANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "persistent hyperplastic primary vitreous, autosomal dominant", "shortest_name_length": 6}
{"curie": "MONDO:0011015", "names": ["CTAA2", "CTRCT24", "CATARACT 24", "cataract 24", "cataract type 24", "anterior polar cataract 2", "Anterior polar cataract 2", "Cataract, anterior polar 2", "anterior polar cataract 24", "CATARACT 24, ANTERIOR POLAR", "Cataract, Anterior Polar, 2", "CATARACT, ANTERIOR POLAR, 2", "cataract, anterior polar, 2", "cataract 24, anterior polar"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 24", "shortest_name_length": 5}
{"curie": "UMLS:C2111708", "names": ["Appendix Large Cell Neuroendocrine Carcinoma", "large cell neuroendocrine carcinoma of appendix", "large cell neuroendocrine carcinoma of appendix (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "large cell neuroendocrine carcinoma of appendix", "shortest_name_length": 44}
{"curie": "MONDO:0009701", "names": ["myopathy, granulovacuolar lobular, with electrical myotonia", "Myopathy, Granulovacuolar Lobular, with Electrical Myotonia", "MYOPATHY, GRANULOVACUOLAR LOBULAR, WITH ELECTRICAL MYOTONIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy, granulovacuolar lobular, with electrical myotonia", "shortest_name_length": 59}
{"curie": "MONDO:0013430", "names": ["MGORS3", "MEIER-GORLIN SYNDROME 3", "Meier-Gorlin syndrome 3", "Meier-GORLIN syndrome 3", "ORC6 Meier-Gorlin syndrome", "Meier-Gorlin syndrome type 3", "Meier-Gorlin syndrome caused by mutation in ORC6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meier-Gorlin syndrome 3", "shortest_name_length": 6}
{"curie": "MONDO:0011043", "names": ["MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE, AND PSYCHOMOTOR DELAY", "Myelodysplasia, Immunodeficiency, Facial Dysmorphism, Short Stature, and Psychomotor Delay", "myelodysplasia, immunodeficiency, facial dysmorphism, short stature, and psychomotor delay"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myelodysplasia, immunodeficiency, facial dysmorphism, short stature, and psychomotor delay", "shortest_name_length": 90}
{"curie": "MONDO:0030681", "names": ["IMD94", "immunodeficiency 94 with autoinflammation and dysmorphic facies", "IMMUNODEFICIENCY 94 WITH AUTOINFLAMMATION AND DYSMORPHIC FACIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 94 with autoinflammation and dysmorphic facies", "shortest_name_length": 5}
{"curie": "MONDO:0035295", "names": ["congenital primary megaureter, refluxing and obstructed form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital primary megaureter, refluxing and obstructed form", "shortest_name_length": 60}
{"curie": "UMLS:C1334797", "names": ["Monomorphic B-Cell PTLD", "Monomorphic B-Cell Post-Transplant Lymphoproliferative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Monomorphic B-Cell Post-Transplant Lymphoproliferative Disorder", "shortest_name_length": 23}
{"curie": "MONDO:0008352", "names": ["pupillary membrane", "membrane; pupillary", "pupillary; membrane", "pupillary membrane disorder", "Pathologic Pupillary membrane", "PUPILLARY MEMBRANE, PERSISTENCE OF", "Pupillary Membrane, Persistence Of", "pupillary membrane, persistence of", "pupillary membrane disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pupillary membrane, persistence of", "shortest_name_length": 18}
{"curie": "UMLS:C0855061", "names": ["Relapsed Liposarcoma", "Liposarcoma Recurrent", "Recurrent Liposarcoma", "Liposarcoma recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liposarcoma recurrent", "shortest_name_length": 20}
{"curie": "MONDO:0014485", "names": ["PCH1C", "pontocerebellar hypoplasia type 1C", "PONTOCEREBELLAR HYPOPLASIA, TYPE 1C", "pontocerebellar hypoplasia, type 1C", "EXOSC8 pontocerebellar hypoplasia type 1", "pontocerebellar hypoplasia type 1 caused by mutation in EXOSC8", "hypomyelination with spinal muscular atrophy and cerebellar hypoplasia", "HYPOMYELINATION WITH SPINAL MUSCULAR ATROPHY AND CEREBELLAR HYPOPLASIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pontocerebellar hypoplasia, type 1C", "shortest_name_length": 5}
{"curie": "MONDO:0019840", "names": ["acropectororenal dysplasia", "acro-pectoro-renal field defect", "brachydactyly, absent pectoral muscles and agenesis/hypoplasia of kidneys"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acropectororenal dysplasia", "shortest_name_length": 26}
{"curie": "UMLS:C0877357", "names": ["Relapsed Gallbladder Cancer", "Recurrent Gallbladder Cancer", "Gallbladder Cancer, Recurrent", "Relapsed Cancer of Gallbladder", "Recurrent Cancer of Gallbladder", "Gallbladder carcinoma recurrent", "Recurrent Gallbladder Carcinoma", "Relapsed Cancer of the Gallbladder", "Recurrent Cancer of the Gallbladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Cancer of Gallbladder", "shortest_name_length": 27}
{"curie": "UMLS:C1710064", "names": ["Severed Digit", "Severed Finger Or Toe", "Severed Digit Finger Or Toe"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Severed Finger Or Toe", "shortest_name_length": 13}
{"curie": "MONDO:0007085", "names": ["SHOKEIR SYNDROME", "Shokeir syndrome", "Alopecia, epilepsy, pyorrhea, mental subnormality", "alopecia, epilepsy, pyorrhea, mental subnormality", "alopecia-epilepsy-pyorrhea-intellectual disability syndrome", "Alopecia-epilepsy-pyorrhea-intellectual disability syndrome", "alopecia, psychomotor epilepsy, pyorrhea, and mental subnormality", "Alopecia, psychomotor epilepsy, pyorrhea, and mental subnormality", "ALOPECIA, PSYCHOMOTOR EPILEPSY, PYORRHEA, AND MENTAL SUBNORMALITY", "congenital universal alopecia, epilepsy, mental subnormality and pyorrhea", "Congenital universal alopecia, epilepsy, mental subnormality and pyorrhea", "Alopecia, psychomotor epilepsy, periodontal pyorrhea, intellectual disability syndrome", "Alopecia, psychomotor epilepsy, periodontal pyorrhoea, intellectual disability syndrome", "Alopecia, psychomotor epilepsy, periodontal pyorrhea, intellectual disability syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alopecia-epilepsy-pyorrhea-intellectual disability syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0005550", "names": ["ID", "Infection", "INFECTION", "infection", "infectious", "Infectious", "Infection, NOS", "Clinical Infection", "clinical infection", "INFECTIOUS DISEASE", "Infective disorder", "Disease;infectious", "infectious disease", "Infectious disease", "contagious disease", "Contagious disease", "Infectious Disease", "Infectious Diseases", "infectious; disease", "infectious disorder", "Infectious Disorder", "Disease, Infectious", "contagious diseases", "Infectious diseases", "infectious diseases", "Infectious Disorders", "Communicable disease", "Communicable Disease", "communicable disease", "Diseases, Infectious", "Infection Unspecified", "Disease, Communicable", "communicable diseases", "Communicable Diseases", "transmissible disease", "Unspecified Infection", "Communicable diseases", "Infectious disease NOS", "microbial colonization", "Diseases, Communicable", "Contagious disease, NOS", "Infectious disease, NOS", "Disease due to infection", "Communicable disease, NOS", "Disorder due to infection", "Transmissible disease, NOS", "RNDx infection unspecified", "Infections and infestations", "disease by infectious agent", "Infectious disease (disorder)", "infectious disease (diagnosis)", "communicable infectious disease", "disease caused by microorganism", "Infectious or communicable disease", "Infectious Diseases and Manifestations", "RNDx infection unspecified (diagnosis)", "infectious diseases and manifestations", "Contagious disease (navigational concept)", "Communicable disease (navigational concept)", "Adenovirus infection in conditions classified elsewhere and of unspecified site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infectious disease", "shortest_name_length": 2}
{"curie": "MONDO:0012788", "names": ["CHDS9", "CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 9", "coronary heart disease, susceptibility to, 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coronary heart disease, susceptibility to, 9", "shortest_name_length": 5}
{"curie": "UMLS:C4521873", "names": ["Stage IA", "Stage IA Pancreatic Cancer", "Stage IA Pancreatic Cancer AJCC v8", "Stage IA Exocrine Pancreatic Cancer AJCC v8", "Stage IA Exocrine Pancreatic Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Pancreatic Cancer AJCC v8", "shortest_name_length": 8}
{"curie": "UMLS:C4763555", "names": ["Monoclonal Gammopathy of Renal Significance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Monoclonal Gammopathy of Renal Significance", "shortest_name_length": 43}
{"curie": "MONDO:0020550", "names": ["gestational choriocarcinoma", "Gestational choriocarcinoma", "Gestational Choriocarcinoma", "Choriocarcinoma, gestational", "Gestational chorioepithelioma", "Gestational chorionepithelioma", "gestational chorionepithelioma", "molar pregnancy with choriocarcinoma", "Molar pregnancy with choriocarcinoma", "Gestational choriocarcinoma (disorder)", "Molar pregnancy with chorioepithelioma", "Molar pregnancy with chorionepithelioma", "gestational choriocarcinoma (morphologic abnormality)", "Gestational choriocarcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gestational choriocarcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0014788", "names": ["LGMD2W", "MDRCMTT", "LGMD type 2W", "LIMS2-related LGM", "Limb girdle muscular dystrophy type 2W", "Limb-girdle muscular dystrophy type 2W", "muscular dystrophy, limb-girdle, type 2W", "muscular dystrophy, limb-girdle, type 2w", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2W", "LIMS2-related limb-girdle muscular dystrophy", "LIMS2-related limb girdle muscular dystrophy", "LIMS2 autosomal recessive limb-girdle muscular dystrophy", "Autosomal recessive limb-girdle muscular dystrophy type 2W", "autosomal recessive limb-girdle muscular dystrophy type 2W", "Autosomal recessive limb girdle muscular dystrophy type 2W", "LIM zinc finger domain containing 2-related limb girdle muscular dystrophy", "autosomal recessive limb-girdle muscular dystrophy caused by mutation in LIMS2", "MUSCULAR DYSTROPHY, AUTOSOMAL RECESSIVE, WITH CARDIOMYOPATHY AND TRIANGULAR TONGUE", "muscular dystrophy, autosomal recessive, with cardiomyopathy and triangular tongue", "LIM zinc finger domain containing 2-related limb girdle muscular dystrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive limb-girdle muscular dystrophy type 2W", "shortest_name_length": 6}
{"curie": "UMLS:C2747905", "names": ["Destructive thyroiditis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Destructive thyroiditis", "shortest_name_length": 23}
{"curie": "MONDO:0018838", "names": ["agyria", "Agyria", "Agyrias", "macrogyria", "pachygyria", "Lissencephaly", "lissencephaly", "Agyria diffuse", "Lissencephalia", "Lissencephalies", "Agyria (diagnosis)", "Broad gyri of cerebrum", "large gyri of cerebrum", "lissencephaly (disease)", "Lissencephaly pachygyria", "Pachygyria/lissencephaly", "Lissencephaly (disorder)", "lissencephaly (diagnosis)", "lissencephaly spectrum disorders", "Fewer or absent grooves in brain", "congenital malformation brain agyria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lissencephaly spectrum disorders", "shortest_name_length": 6}
{"curie": "UMLS:C4527066", "names": ["stage 0 Merkel cell carcinoma", "Pathologic Stage 0 Merkel Cell Carcinoma AJCC v8", "pathologic stage 0 Merkel cell carcinoma AJCC v8", "Pathologic Stage 0 Neuroendocrine Carcinoma of the Skin AJCC v8", "pathologic stage 0 neuroendocrine carcinoma of the skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage 0 Merkel Cell Carcinoma AJCC v8", "shortest_name_length": 29}
{"curie": "UMLS:C5238464", "names": ["Midgut Neuroendocrine Tumor G2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Midgut Neuroendocrine Tumor G2", "shortest_name_length": 30}
{"curie": "MONDO:0001227", "names": ["Chronic tympanitis", "Chronic myringitis", "Myringitis;chronic", "chronic tympanitis", "chronic myringitis", "chronic; tympanitis", "myringitis; chronic", "tympanitis, chronic", "chronic; myringitis", "tympanitis; chronic", "Chronic tympanitis, NOS", "Chronic myringitis, NOS", "Chronic tympanitis (disorder)", "chronic myringitis (diagnosis)", "Chronic tympanitis (diagnosis)", "Chronic myringitis, unspecified ear", "Chronic myringitis without otitis media", "Chronic myringitis without mention of otitis media"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic tympanitis", "shortest_name_length": 18}
{"curie": "MONDO:0009859", "names": ["PHAVER syndrome", "PHAVER SYNDROME", "Powell-Chandra-Saal syndrome", "Powell Chandra Saal syndrome", "Vertebral, radial, congenital heart, and ear defects", "pterygia heart defects autosomal recessive inheritance vertebral defects Ear anomalies and radial defects", "Pterygia, heart anomaly, autosomal recessive inheritance, vertebral defect, ear anomaly, radial defect syndrome", "PHAVER (pterygia, heart anomaly, autosomal recessive inheritance, vertebral defect, ear anomaly, radial defect) syndrome", "Pterygia, heart anomaly, autosomal recessive inheritance, vertebral defect, ear anomaly, radial defect syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PHAVER syndrome", "shortest_name_length": 15}
{"curie": "UMLS:C0162387", "names": ["trochanteric fracture", "Trochanteric Fractures", "trochanteric fractures", "Fractures, Trochanteric"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Trochanteric Fractures", "shortest_name_length": 21}
{"curie": "MONDO:0022891", "names": ["craniosynostosis Maroteaux Fonfria type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniosynostosis Maroteaux Fonfria type", "shortest_name_length": 39}
{"curie": "UMLS:C1333830", "names": ["Grade 1 Cutaneous Follicular Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade 1 Cutaneous Follicular Lymphoma", "shortest_name_length": 37}
{"curie": "MONDO:0012422", "names": ["T1D19", "IDDM19", "type 1 diabetes mellitus 19", "TYPE 1 DIABETES MELLITUS 19", "insulin-dependent diabetes mellitus 19", "Insulin-Dependent Diabetes Mellitus 19", "Diabetes Mellitus, Insulin-Dependent, 19", "DIABETES MELLITUS, INSULIN-DEPENDENT, 19", "diabetes mellitus, insulin-dependent, 19", "DIABETES MELLITUS, INSULIN-DEPENDENT, 19 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type 1 diabetes mellitus 19", "shortest_name_length": 5}
{"curie": "UMLS:C1333963", "names": ["HNET", "Liver Carcinoid Tumor", "Hepatic Carcinoid Tumor", "Carcinoid Tumor of Liver", "Liver Neuroendocrine Tumor", "Carcinoid tumor of the liver", "Carcinoid Tumor of the Liver", "Hepatic Neuroendocrine Tumor", "Hepatic neuroendocrine tumor", "Carcinoid tumour of the liver", "Hepatic neuroendocrine tumour", "Primary Liver Neuroendocrine Tumor", "Primary Hepatic Neuroendocrine Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carcinoid tumor of the liver", "shortest_name_length": 4}
{"curie": "UMLS:C1336841", "names": ["Type A LyP", "lymphomatoid papulosis type a", "Type A Lymphomatoid Papulosis", "lymphomatoid papulosis, type A", "lymphomatoid papulosis, type A (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphomatoid papulosis, type A", "shortest_name_length": 10}
{"curie": "MONDO:0017398", "names": ["3MC syndrome", "oculopalatoskeletal syndrome", "craniofacial-ulnar-renal syndrome", "Craniofacial ulnar renal syndrome", "Craniofacial-ulnar-renal syndrome", "Craniofacial ulnar renal syndrome (disorder)", "Malpuech-Michels-Mingarelli-Carnevale syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "3MC syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0017614", "names": ["Young-Hughes syndrome", "Young Hughes syndrome", "X-linked intellectual disability - short stature – obesity", "mental retardation-short stature-obesity-hypogonadism syndrome", "Sex-linked mental retardation, short stature, obesity and hypogonadism", "Sex-linked intellectual disability, short stature, obesity and hypogonadism", "X-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome", "X-linked intellectual disability, hypogonadism, ichthyosis, obesity, short stature syndrome", "X-linked intellectual disability, hypogonadism, ichthyosis, obesity, short stature syndrome (disorder)", "X-linked intellectual disability, hypogonadism, ichthyosis, obesity, short stature syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome", "shortest_name_length": 21}
{"curie": "MONDO:0020087", "names": ["Genetic lipodystrophy", "genetic lipodystrophy", "genetic lipodystrophy (disease)", "Genetic lipodystrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genetic lipodystrophy", "shortest_name_length": 21}
{"curie": "MONDO:0016821", "names": ["shoulder girdle defect mental retardation familial", "shoulder girdle defect intellectual disability familial", "shoulder and girdle defects-familial intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "shoulder and girdle defects-familial intellectual disability syndrome", "shortest_name_length": 50}
{"curie": "MONDO:0017090", "names": ["Midline brain malformation", "midline cerebral malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "midline cerebral malformation", "shortest_name_length": 26}
{"curie": "UMLS:C4053943", "names": ["Testicular Hypotrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular Hypotrophy", "shortest_name_length": 21}
{"curie": "MONDO:0016431", "names": ["CMT2M", "Charcot-Marie-Tooth disease type 2M", "Charcot-Marie-Tooth disease type 2M (diagnosis)", "Autosomal dominant Charcot-Marie-Tooth disease type 2M", "autosomal dominant Charcot-Marie-Tooth disease type 2M", "Autosomal dominant Charcot-Marie-Tooth disease type 2M (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant Charcot-Marie-Tooth disease type 2M", "shortest_name_length": 5}
{"curie": "UMLS:C5239193", "names": ["Post-treatment Disease Complication", "Post-treatment disease complications"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post-treatment Disease Complication", "shortest_name_length": 35}
{"curie": "MONDO:0016150", "names": ["integrinopathy", "qualitative or quantitative defects of integrin alpha-7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of integrin alpha-7", "shortest_name_length": 14}
{"curie": "MONDO:0012842", "names": ["CMM7", "melanoma, cutaneous malignant, 7", "melanoma, cutaneous malignant, susceptibility to, 7", "MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melanoma, cutaneous malignant, susceptibility to, 7", "shortest_name_length": 4}
{"curie": "MONDO:0012962", "names": ["MVCD2", "microvascular complications of diabetes 2", "end-stage renal disease, diabetic, susceptibility to", "END-STAGE RENAL DISEASE, DIABETIC, SUSCEPTIBILITY TO", "proliferative retinopathy, diabetic, susceptibility to", "PROLIFERATIVE RETINOPATHY, DIABETIC, SUSCEPTIBILITY TO", "EPO microvascular complications of diabetes, susceptibility", "MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 2", "microvascular complications of diabetes, susceptibility to, 2", "microvascular complications of diabetes, susceptibility to, type 2", "microvascular complications of diabetes, susceptibility caused by mutation in EPO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microvascular complications of diabetes, susceptibility to, 2", "shortest_name_length": 5}
{"curie": "MONDO:0004764", "names": ["fibular collateral ligament bursitis", "Fibular collateral ligament bursitis", "bursitis of fibular collateral ligament", "bursitis of fibular collateral ligament (diagnosis)", "Inflammation of subtendinous bursa of biceps femoris inferior muscle", "Inflammation of subtendinous bursa of biceps femoris inferior muscle (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibular collateral ligament bursitis", "shortest_name_length": 36}
{"curie": "MONDO:0014601", "names": ["SCAR20", "SNX14 autosomal recessive cerebellar ataxia", "autosomal recessive spinocerebellar ataxia 20", "spinocerebellar ataxia, autosomal recessive 20", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20", "Autosomal recessive spinocerebellar ataxia type 20", "autosomal recessive spinocerebellar ataxia type 20", "spinocerebellar ataxia, autosomal recessive type 20", "SCAR20 - autosomal recessive spinocerebellar ataxia type 20", "autosomal recessive cerebellar ataxia caused by mutation in SNX14", "Intellectual disability-coarse face-macrocephaly-cerebellar hypoplasia syndrome", "intellectual disability-coarse face-macrocephaly-cerebellar hypoplasia syndrome", "intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome", "Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome", "Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome", "Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome (disorder)", "Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive spinocerebellar ataxia 20", "shortest_name_length": 6}
{"curie": "MONDO:0014790", "names": ["CDG2P", "CDGIIp", "CDG-IIp", "CDG IIp", "CDGIIdp", "TMEM199-CDG", "CDG syndrome type IIp", "congenital disorder of glycosylation type 2p", "Congenital disorder of glycosylation type 2p", "TMEM199 congenital disorder of glycosylation", "Congenital disorder of glycosylation type IIp", "congenital disorder of glycosylation type IIp", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIp", "congenital disorder of glycosylation, type IIp", "carbohydrate deficient glycoprotein syndrome type IIp", "Carbohydrate deficient glycoprotein syndrome type IIp", "CDG (congenital disorder of glycosylation) syndrome type IIp", "Transmembrane protein 199 congenital disorder of glycosylation", "Transmembrane protein 199 congenital disorder of glycosylation (disorder)", "TMEM199-CDG - transmembrane protein 199 congenital disorder of glycosylation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "TMEM199-CDG", "shortest_name_length": 5}
{"curie": "UMLS:C1336471", "names": ["Stage I Osteosarcoma", "Stage I Osteogenic Sarcoma", "Stage I Osteosarcoma AJCC v7", "Stage I Osteosarcoma  AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Osteosarcoma AJCC v7", "shortest_name_length": 20}
{"curie": "MONDO:0003088", "names": ["Intramuscular angioma", "intramuscular angioma", "Intramuscular Angioma", "Intramuscular Hemangioma", "intramuscular hemangioma", "Intramuscular hemangioma", "Hemangioma, Intramuscular", "Intramuscular Hemangiomas", "intramuscular haemangioma", "intramuscular; hemangioma", "Intramuscular haemangioma", "hemangioma; intramuscular", "Hemangiomas, Intramuscular", "intramuscular hemangioma (morphologic abnormality)", "Intramuscular hemangioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intramuscular hemangioma", "shortest_name_length": 21}
{"curie": "OMIM:616814", "names": ["PREMBL", "PREMBL1", "PREIMPLANTATION EMBRYONIC LETHALITY 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 6}
{"curie": "MONDO:0017489", "names": ["ulnar hemimelia, unilateral", "ulnar longitudinal meromelia, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ulnar hemimelia, unilateral", "shortest_name_length": 27}
{"curie": "MONDO:0005836", "names": ["Neoplasm;genital;M", "male genital cancer", "Genital cancer male", "male genital neoplasm", "Male Genital Neoplasm", "Genital Neoplasm, Male", "Neoplasm, Male Genital", "Male Genital Neoplasms", "Genital Neoplasms, Male", "Neoplasms, Male Genital", "male reproductive cancer", "Neoplasm malig;genital sys;M", "Tumor of male genital organs", "Tumour of male genital organs", "Cancer of male genital organs", "Neoplasm of male genital organ", "male reproductive organ cancer", "Male Reproductive System Tumor", "neoplasm of male genital organ", "Male reprod. system cancer, NOS", "male genital cancer (diagnosis)", "Male reproductive tract neoplasm", "Tumor of Male Reproductive System", "cancer of male reproductive organ", "tumor of male Reproductive system", "male reproductive system neoplasm", "tumor of male reproductive system", "Male reproductive system neoplasm", "Male Reproductive System Neoplasm", "neoplasm of the male genital system", "Neoplasm of Male Reproductive System", "Male reproductive tract neoplasm NOS", "Male reproductive system cancer, NOS", "Tumor of the Male Reproductive System", "malignant tumor of male genital organ", "Malignant tumor of male genital organ", "Malignant tumour of male genital organ", "malignant Male reproductive system tumor", "Neoplasm of the Male Reproductive System", "malignant male reproductive system tumor", "malignant neoplasm of male genital organ", "Malignant Male Reproductive System Tumor", "Neoplasm of male genital organ (disorder)", "malignant neoplasm of male genital organs", "malignant male reproductive organ neoplasm", "Malignant neoplasms of male genital organs", "malignant tumor of male reproductive system", "malignant tumor of Male reproductive system", "malignant Male reproductive system neoplasm", "Malignant Male Reproductive System Neoplasm", "malignant male reproductive system neoplasm", "malignant tumor of male Reproductive system", "Malignant Tumor of Male Reproductive System", "malignant neoplasm of male reproductive organ", "Malignant neoplasm of male genital organ, NOS", "malignant neosplasm of the male genital system", "malignant neoplasm of Male reproductive system", "Malignant Neoplasm of Male Reproductive System", "malignant neoplasm of male reproductive system", "Malignant Tumor of the Male Reproductive System", "malignant tumor of the Male reproductive system", "malignant tumor of the male reproductive system", "Malignant tumor of male genital organ (disorder)", "malignant neoplasm of male genital organ or tract", "malignant neoplasm of the male reproductive system", "malignant neoplasm of the Male reproductive system", "Malignant Neoplasm of the Male Reproductive System", "Malignant neoplasms of male genital organs (C60-C63)", "malignant neoplasm of male genital organs (diagnosis)", "Malignant neoplasm of male genital organ or tract NOS", "Malignant neoplasm of male genital organ, unspecified", "malignant neoplasm of male genital organ, site unspecified", "Malignant neoplasm of male genital organ, site unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "male reproductive organ cancer", "shortest_name_length": 18}
{"curie": "MONDO:0008230", "names": ["SAPX", "peroxidase, salivary", "PEROXIDASE, SALIVARY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxidase, salivary", "shortest_name_length": 4}
{"curie": "MONDO:0005913", "names": ["Pappataci", "sandfly fever", "Sandfly fever", "Sandfly Fever", "FEVER, SANDFLY", "fever; sandfly", "Sandfly Fevers", "sandfly; fever", "Pappataci fever", "Pappataci Fever", "pappataci fever", "fever; pappataci", "pappataci; fever", "FEVER, THREE-DAY", "PLEBOTOMUS FEVER", "Pappataci Fevers", "FEVER, PAPPATACI", "PHLEBOTOMUS FEVER", "Phlebotomus fever", "phlebotomus fever", "Phlebotomus Fever", "fever; phlebotomus", "Phlebotomus Fevers", "Sandfly fever, NOS", "phlebotomus; fever", "phlebotomus fever (diagnosis)", "Sandfly-borne arboviral fever", "Sandfly-borne Bunyavirus fever", "Sandfly-borne bunyavirus fever", "Sandfly-borne phleboviral disease", "Sandfly-borne phleboviral disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phlebotomus fever", "shortest_name_length": 9}
{"curie": "UMLS:C5204122", "names": ["C3 Glomerulopathy with Monoclonal Gammopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "C3 Glomerulopathy with Monoclonal Gammopathy", "shortest_name_length": 44}
{"curie": "MONDO:0007332", "names": ["SHFLD", "SHFLD1", "TH-SHFM", "SHFLD syndrome", "Cleft hand absent tibia", "cleft hand absent tibia", "cleft hand and absent tibia", "CLEFT HAND AND ABSENT TIBIA", "Cleft Hand And Absent Tibia", "aplasia of tibia with ectrodactyly", "Aplasia of tibia with ectrodactyly", "APLASIA OF TIBIA WITH ECTRODACTYLY", "Tibial aplasia-ectrodactyly syndrome", "Tibial hemimelia-ectrodactyly syndrome", "Tibial hemimelia ectrodactyly syndrome", "ectrodactyly with aplasia of long bones", "ECTRODACTYLY WITH APLASIA OF LONG BONES", "Ectrodactyly with aplasia of long bones", "Tibial aplasia and ectrodactyly syndrome", "SHFM associated with aplasia of long bones", "Tibial hemimelia with split hand/foot malformation", "Tibial aplasia with split-hand-split-foot deformity", "tibial aplasia with split-hand-split-foot deformity", "Tibial aplasia and ectrodactyly syndrome (disorder)", "tibial aplasia with split-hand/split-foot deformity", "TIBIAL APLASIA WITH SPLIT-HAND/SPLIT-FOOT DEFORMITY", "Aplasia of tibia with split-hand/split-foot deformity", "Aplasia of tibia with split hand split foot deformity", "split-hand-foot malformation with long bone deficiency", "Split hand/foot malformation with long bone deficiency", "Split hand foot malformation with long bone deficiency", "Split-hand-foot malformation with long bone deficiency", "split-hand/foot malformation with long bone deficiency", "SPLIT-HAND/FOOT MALFORMATION WITH LONG BONE DEFICIENCY", "SPLIT-HAND/FOOT MALFORMATION WITH LONG BONE DEFICIENCY 1", "split-hand/foot malformation with long bone deficiency 1", "Split-Hand-Foot Malformation With Long Bone Deficiency 1", "Split-hand/foot malformation associated with aplasia of long bones"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "split-hand/foot malformation with long bone deficiency 1", "shortest_name_length": 5}
{"curie": "UMLS:C3888703", "names": ["Medical device site discomfort"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Medical device site discomfort", "shortest_name_length": 30}
{"curie": "MONDO:0009828", "names": ["PALANT CLEFT PALATE SYNDROME", "Palant cleft palate syndrome", "palant cleft palate syndrome", "Unusual facies, cleft palate, mental retardation, and limb abnormalities", "unusual facies, cleft palate, mental retardation, and limb abnormalities", "unusual facies, cleft palate, intellectual disability, and limb abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "palant cleft palate syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0008982", "names": ["CACD", "CACD1", "choroid; dystrophy", "dystrophy; choroid", "Choroidal dystrophy", "choroidal dystrophy", "choroidal dystrophies", "areolar atrophy of the macula", "Areolar atrophy of the macula", "Choroidal dystrophy (disorder)", "choroidal dystrophy (diagnosis)", "Central areolar choroidal sclerosis", "Choroidal dystrophy central areolar", "central areolar choroidal dystrophy", "central areolar choroidal sclerosis", "choroidal dystrophy central areolar", "Central areolar choroidal dystrophy", "Choroidal Dystrophy, Central Areolar", "CHOROIDAL DYSTROPHY, CENTRAL AREOLAR", "choroidal dystrophy, central areolar, 1", "Central areolar choroidal sclerosis (disorder)", "central areolar choroidal dystrophy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central areolar choroidal dystrophy", "shortest_name_length": 4}
{"curie": "UMLS:C1333039", "names": ["CLL with IGVH SHM", "Postgerminal Center Chronic Lymphocytic Leukemia", "Chronic Lymphocytic Leukemia with Immunoglobulin Heavy Chain Variable-Region Gene Somatic Hypermutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic Lymphocytic Leukemia with Immunoglobulin Heavy Chain Variable-Region Gene Somatic Hypermutation", "shortest_name_length": 17}
{"curie": "MONDO:0041755", "names": ["twin reversal arterial perfusion syndrome", "Twin reversal arterial perfusion syndrome", "TRAP- twin reversal arterial perfusion syndrome", "Twin reversal arterial perfusion syndrome (disorder)", "twin reversal arterial perfusion syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "twin reversal arterial perfusion syndrome", "shortest_name_length": 41}
{"curie": "MONDO:0009070", "names": ["D-glycericacidemia", "D-GLYCERIC ACIDURIA", "D-Glyceric Acidemia", "D-Glyceric aciduria", "d-glyceric aciduria", "D-glyceric acidemia", "D-GLYCERIC ACIDEMIA", "D-Glyceric Aciduria", "D-glyceric aciduria", "glycerate kinase deficiency", "GLYCERATE KINASE DEFICIENCY", "Glycerate Kinase Deficiency", "D-Glycerate kinase deficiency", "D-glycerate kinase deficiency", "Deficiency of glycerate kinase", "D-Glyceric aciduria (disorder)", "deficiency of glycerate kinase", "non ketotic hyperglycinemia syndrome", "Deficiency of glycerate kinase (disorder)", "deficiency of glycerate kinase (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "D-glyceric aciduria", "shortest_name_length": 18}
{"curie": "MONDO:0000979", "names": ["azul", "AZUL", "Azul", "Lota", "Tina", "PINTA", "Pinta", "pinta", "carate", "CARATE", "Carate", "Empeines", "Pinta, NOS", "Carate, NOS", "MAL DEL PINTO", "pinta; papule", "pinta disease", "Mal del pinto", "papule; pinta", "chancre; pinta", "Pinta [carate]", "papule; carate", "Papule of pinta", "chancre; carate", "Pintid of pinta", "Pinta (disorder)", "Papule of carate", "Chancre of pinta", "Pintid of carate", "Chancre of carate", "pinta (diagnosis)", "Late pinta lesion", "Pinta, late lesion", "Pinta, unspecified", "Primary pinta lesion", "Late cutaneous pinta", "pinta; lesions, late", "lesions; pinta, late", "Pinta, mixed lesions", "Pinta, primary lesion", "late lesions of pinta", "pinta; lesions, mixed", "pinta; primary lesion", "Late lesions of pinta", "lesion; primary, pinta", "Mixed lesions of pinta", "primary; lesion, pinta", "pinta; lesion, primary", "mixed lesions of pinta", "lesions; pinta, primary", "primary; lesion, carate", "lesion; primary, carate", "pinta; lesions, primary", "Primary papule of pinta", "primary lesions of pinta", "Primary chancre of pinta", "Primary papule of carate", "Primary lesions of pinta", "Intermediate pinta lesion", "Primary chancre of carate", "Papule (primary) of pinta", "pinta; skin lesions, mixed", "Pinta, intermediate lesion", "Chancre (primary) of pinta", "pinta; lesions, skin, mixed", "Intermediate lesion of pinta", "Treponema carateum infection", "Mixed cutaneous pinta lesion", "Intermediate lesions of pinta", "intermediate lesions of pinta", "Pinta, late lesion (disorder)", "infection by Treponema carateum", "Infection by Treponema carateum", "Pinta, primary lesion (disorder)", "late lesions of pinta (diagnosis)", "mixed lesions of pinta (diagnosis)", "infection due to Treponema carateum", "primary lesions of pinta (diagnosis)", "Mixed cutaneous pinta lesion (disorder)", "Intermediate lesion of pinta (disorder)", "intermediate lesions of pinta (diagnosis)", "endemic treponematosis caused by Treponema carateum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pinta disease", "shortest_name_length": 4}
{"curie": "MONDO:0010217", "names": ["xerodermic idiocy", "Xerodermic idiocy", "DeSanctis Cacchione syndrome", "Desanctis-Cacchione Syndrome", "DeSanctis-Cacchione syndrome", "De Sanctis-Cacchione Syndrome", "de Sanctis-Cacchione syndrome", "de sanctis-cacchione syndrome", "De Sanctis-Cacchione syndrome", "DE SANCTIS-CACCHIONE SYNDROME", "Xerodermic idiocy of de Sanctis and Cacchione", "xeroderma pigmentosum with neurologic manifestation", "Xeroderma pigmentosum, mental deficiency, dwarfism, and gonadal hypoplasia", "intellectual disability, dwarfism, and gonadal hypoplasia due to xeroderma pigmentosum", "intellectual disability, dwarfism, and gonadal hypoplasia due to xeroderma pigmentosum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "de Sanctis-Cacchione syndrome", "shortest_name_length": 17}
{"curie": "UMLS:C1334714", "names": ["Metastatic Breast Carcinoid Tumor", "Metastatic Carcinoid Tumor of Breast", "Metastatic Carcinoid Tumor of the Breast", "Metastatic Breast Neuroendocrine Tumor G1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Breast Neuroendocrine Tumor G1", "shortest_name_length": 33}
{"curie": "MONDO:0016680", "names": ["high-grade astrocytoma", "high-grade astrocytic tumor", "High-Grade Astrocytic Tumor", "high grade astrocytic tumor", "High Grade Astrocytic Tumor", "High-Grade Astrocytic Neoplasm", "high-grade astrocytic neoplasm", "high grade astrocytic neoplasm", "High Grade Astrocytic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "high grade astrocytic tumor", "shortest_name_length": 22}
{"curie": "UMLS:C0038870", "names": ["Supraorbital neuralgia", "Supraorbital Neuralgia", "Neuralgia, Supraorbital", "Supraorbital Neuralgias", "Neuralgias, Supraorbital", "Supraorbital neuralgia (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neuralgia, Supraorbital", "shortest_name_length": 22}
{"curie": "UMLS:C1336265", "names": ["Stage III Mesothelioma", "stage III pleural mesothelioma", "stage III malignant mesothelioma", "stage III mesothelioma of pleura", "Stage III Mesothelioma of Pleura", "stage III mesothelioma of the pleura", "Stage III Mesothelioma of the Pleura", "stage III pleural mesothelioma AJCC v7", "Stage III Pleural Malignant Mesothelioma", "Stage III Pleural Malignant Mesothelioma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Pleural Malignant Mesothelioma AJCC v7", "shortest_name_length": 22}
{"curie": "MONDO:0009233", "names": ["Saito-Kuba-Tsuruta syndrome", "Saito Kuba Tsuruta syndrome", "Fibulo ulnar hypoplasia renal anomalies", "Fibuloulnar hypoplasia with renal abnormalities", "Fibulo-ulnar hypoplasia-renal anomalies syndrome", "Fibulo-ulnar hypoplasia and renal anomalies syndrome", "Fibuloulnar aplasia or hypoplasia with renal abnormalities", "FIBULOULNAR APLASIA OR HYPOPLASIA WITH RENAL ABNORMALITIES", "FIBULOULNAR aplasia or hypoplasia with renal abnormalities", "Fibulo-ulnar hypoplasia and renal anomalies syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fibulo-ulnar hypoplasia-renal anomalies syndrome", "shortest_name_length": 27}
{"curie": "MONDO:0013193", "names": ["TTPP2", "KCNJ18 thyrotoxic periodic paralysis", "THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 2", "thyrotoxic periodic paralysis, susceptibility to, 2", "thyrotoxic periodic paralysis, susceptibility to, type 2", "thyrotoxic periodic paralysis caused by mutation in KCNJ18"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyrotoxic periodic paralysis, susceptibility to, 2", "shortest_name_length": 5}
{"curie": "MONDO:0009761", "names": ["Hygroma", "hygroma", "Hygromas", "hygromas", "Hygroma, NOS", "HYGROMA CYSTIC", "CYSTIC HYGROMA", "cystic Hygroma", "Cystic hygroma", "Hygroma cystic", "cystic hygroma", "Cystic Hygroma", "Cystic Hygromas", "Hygroma, Cystic", "cystic hygromas", "Hygromas, Cystic", "Lymphangioma;cystic", "Cystic lymphangioma", "cystic lymphangioma", "Cystic Lymphangioma", "Cystic Lymphangiomas", "cystic lymphangiomas", "Lymphangioma, Cystic", "lymphangioma; cystic", "Cystic Hygroma Colli", "cystic; lymphangioma", "cystic hygroma, fetal", "Hygroma Colli, Cystic", "Colli, Cystic Hygroma", "Lymphangiomas, Cystic", "nuchal bleb, familial", "Cystic hygroma (disorder)", "cystic hygroma (diagnosis)", "Cystic hygroma of the neck", "macrocystic lymphatic malformation", "Cystic lymphangioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cystic hygroma", "shortest_name_length": 7}
{"curie": "MONDO:0015617", "names": ["genetic gastro-esophageal disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genetic gastro-esophageal disease", "shortest_name_length": 33}
{"curie": "MONDO:0017446", "names": ["Apodia", "apodia", "Absent foot", "Foot agenesis", "Hindpaw apodia", "agenesis; foot", "foot; agenesis", "Agenesis of foot", "Aplasia of the foot", "Agenesis of hindpaw", "congenital absence of foot", "Congenital absence of foot", "Agenesis of foot (disorder)", "Congenital absence of hindpaw", "congenital absence of foot and toe", "Congenital absence of foot (disorder)", "Congenital absence of foot and toe(s)", "congenital deformity absence foot and toe", "Transverse deficiency lower limb - ankle level", "congenital absence of foot and toe (diagnosis)", "Congenital absence of unspecified foot and toe(s)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "apodia", "shortest_name_length": 6}
{"curie": "MONDO:0044637", "names": ["IOLOD", "dyskinesia, limb and orofacial, infantile-onset", "DYSKINESIA, LIMB AND OROFACIAL, INFANTILE-ONSET", "Infantile-onset orofacial-trunk-limbs dyskinesia", "infantile-onset orofacial-trunk-limbs dyskinesia", "Infantile-onset orofacial, trunk, limbs dyskinesia", "infantile-onset generalized dyskinesia with orofacial involvement", "Infantile-onset generalized dyskinesia with orofacial involvement", "Infantile-onset generalised dyskinesia with orofacial involvement", "Infantile-onset generalized dyskinesia with orofacial involvement (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile-onset generalized dyskinesia with orofacial involvement", "shortest_name_length": 5}
{"curie": "UMLS:C0919600", "names": ["Application site hyperesthesia", "Application site hyperaesthesia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Application site hyperesthesia", "shortest_name_length": 30}
{"curie": "MONDO:0005885", "names": ["neuritis optic", "Neuritis;optic", "Neuritis optic", "Optic Neuritis", "optic neuritis", "NEURITIS OPTIC", "OPTIC NEURITIS", "Optic neuritis", "optic; neuritis", "neuritis; optic", "Neuritis, Optic", "Optic Neuritides", "Neuritides, Optic", "Optic neuritis NOS", "Optic neuritis, NOS", "ON - Optic neuritis", "Optic nerve inflamed", "n.opticus; inflammation", "Optic nerve inflammation", "optic nerve; inflammation", "Optic neuritis (disorder)", "inflammation; optic nerve", "Unspecified optic neuritis", "inflammation; nerve, optic", "optic neuritis (diagnosis)", "Optic neuritis, unspecified", "CRANIAL NERVE II OPTIC NEURITIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "optic neuritis", "shortest_name_length": 14}
{"curie": "UMLS:C0744130", "names": ["diabetic foot infection", "infection diabetic foot", "FOOT INFECTION DIABETIC", "foot diabetic infection", "Diabetic foot infection", "diabetic foot infections"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diabetic foot infection", "shortest_name_length": 23}
{"curie": "UMLS:C3160754", "names": ["Atypical femur fracture", "fracture femur atypical", "Atypical fracture of femur", "atypical fracture of femur", "Atypical fracture of femur (disorder)", "atypical fracture of femur (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypical fracture of femur", "shortest_name_length": 23}
{"curie": "MONDO:0010915", "names": ["DFNA4", "DFNA4A", "autosomal dominant deafness 4A", "deafness, autosomal dominant 4", "Deafness, Autosomal Dominant 4", "DEAFNESS, AUTOSOMAL DOMINANT 4", "DEAFNESS, AUTOSOMAL DOMINANT 4A", "deafness, autosomal dominant 4a", "deafness, autosomal dominant 4A", "deafness, autosomal dominant type 4A", "autosomal dominant nonsyndromic deafness 4A", "MYH14 autosomal dominant nonsyndromic deafness", "autosomal dominant nonsyndromic hearing loss 4A", "autosomal dominant nonsyndromic deafness type 4A", "autosomal dominant nonsyndromic deafness caused by mutation in MYH14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 4A", "shortest_name_length": 5}
{"curie": "MONDO:0016695", "names": ["OLIGODENDROGLIOMA", "Oligodendroglioma", "oligodendroglioma", "Oligodendrogliomas", "oligodendrogliomas", "Oligodendroglioma NOS", "Oligodendroglioma, NOS", "oligodendroglial tumor", "oligodendroglial neoplasm", "Oligodendroglioma (disorder)", "WHO Grade 2 Oligodendroglial Tumor", "WHO Grade II Oligodendroglial Tumor", "WHO grade II oligodendroglial tumor", "well differentiated oligodendroglioma", "Well Differentiated Oligodendroglioma", "WHO Grade 2 Oligodendroglial Neoplasm", "Well-Differentiated Oligodendroglioma", "Oligodendroglioma, Well Differentiated", "Oligodendroglioma, Well-Differentiated", "Well-Differentiated Oligodendrogliomas", "WHO grade II oligodendroglial neoplasm", "WHO Grade II Oligodendroglial Neoplasm", "Oligodendrogliomas, Well-Differentiated", "Oligodendroglioma, Not Otherwise Specified", "Well Differentiated Oligodendroglial Tumor", "well differentiated oligodendroglial tumor", "Oligodendroglioma (morphologic abnormality)", "oligodendroglioma, IDH-mutant and 1p/19q-codeleted grade 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oligodendroglioma", "shortest_name_length": 17}
{"curie": "UMLS:C5668300", "names": ["Thymic Enteric-Type Adenocarcinoma", "Thymic Intestinal-Type Adenocarcinoma", "Thymic Mucinous (Colloid) Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thymic Enteric-Type Adenocarcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0012843", "names": ["ECA5", "GABRB3 childhood absence epilepsy", "susceptibility to childhood absence epilepsy 5", "epilepsy, childhood absence, susceptibility to, 5", "EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 5", "epilepsy, childhood absence, susceptibility to, type 5", "childhood absence epilepsy caused by mutation in GABRB3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, childhood absence, susceptibility to, 5", "shortest_name_length": 4}
{"curie": "UMLS:C0149892", "names": ["parulis", "Parulis", "Gum boil", "gum boil", "boil gums", "boils gum", "Parulides", "gum abscess", "abscess gum", "ABSCESS GUM", "Gum abscess", "Abscess gum", "gum; abscess", "abscess gums", "abscess; gum", "Abscess;gums", "abscessed gums", "gingiva abscess", "gingival abscess", "GINGIVA, ABSCESS", "abscess; gingiva", "gingiva; abscess", "Gingival abscess", "Parulis (disorder)", "gingival abscess (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parulis", "shortest_name_length": 7}
{"curie": "MONDO:0017658", "names": ["hyperekplexia", "Hyperexplexia", "hyperexplexia", "Hyperekplexia", "Hyperekplexias", "startle disease", "Startle disease", "Startle syndrome", "startle syndrome", "Hyperexplexia (finding)", "Increased startle response", "Exaggerated startle response", "Exaggerated acoustic startle response"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperekplexia", "shortest_name_length": 13}
{"curie": "UMLS:C0855053", "names": ["Recurrent Extraosseous Osteosarcoma", "Relapsed Extraskeletal Osteosarcoma", "Recurrent Extraskeletal Osteosarcoma", "Extraskeletal osteosarcoma recurrent", "Extraskeletal Osteosarcoma, Recurrent", "Relapsed Extraskeletal Osteogenic Sarcoma", "Recurrent Extraskeletal Osteogenic Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extraskeletal osteosarcoma recurrent", "shortest_name_length": 35}
{"curie": "UMLS:C0751207", "names": ["Huntington Disease, Akinetic Rigid Variant", "Huntington Disease, Akinetic-Rigid Variant", "Akinetic-Rigid Variant of Huntington Disease", "Akinetic Rigid Variant of Huntington Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Akinetic-Rigid Variant of Huntington Disease", "shortest_name_length": 42}
{"curie": "UMLS:C1707443", "names": ["Colorectal Undifferentiated Carcinoma", "Undifferentiated Colorectal (Colon or Rectal) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Undifferentiated Carcinoma", "shortest_name_length": 37}
{"curie": "UMLS:C4329305", "names": ["Anemia due to Increased Destruction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anemia due to Increased Destruction", "shortest_name_length": 35}
{"curie": "MONDO:0019504", "names": ["SLK", "Theodore syndrome", "Theodores syndrome", "Theodore's syndrome", "Superior limbic keratitis", "superior limbic keratoconjunctivitis", "Superior limbic keratoconjunctivitis", "SLK - Superior limbic keratoconjunctivitis", "Theodore superior limbic keratoconjunctivitis", "Theodores superior limbic keratoconjunctivitis", "Superior limbic keratoconjunctivitis (disorder)", "Theodore's superior limbic keratoconjunctivitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "superior limbic keratoconjunctivitis", "shortest_name_length": 3}
{"curie": "UMLS:C1334715", "names": ["Metastatic Carcinoid Tumor", "Metastatic carcinoid tumor", "Metastatic carcinoid tumour", "Metastatic carcinoid tumor (disorder)", "Metastatic carcinoid tumor (diagnosis)", "neuroendocrine tumor carcinoid metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic carcinoid tumor", "shortest_name_length": 26}
{"curie": "UMLS:C4288004", "names": ["Vulvar Melanocytic Nevus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Melanocytic Nevus", "shortest_name_length": 24}
{"curie": "UMLS:C5419583", "names": ["Refractory Grade 3 Follicular Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Grade 3 Follicular Lymphoma", "shortest_name_length": 38}
{"curie": "MONDO:0017227", "names": ["AIP type 1", "Type 1 AIP", "IgG4-related pancreatitis", "IgG4 related Pancreatitis", "IgG4-related Pancreatitis", "Pancreatitis, IgG4-related", "IgG4-related Pancreatitides", "Autoimmune pancreatitis type 1", "Type 1 Autoimmune Pancreatitis", "autoimmune pancreatitis type 1", "lymphoplasmacytic sclerosing pancreatitis", "Lymphoplasmacytic sclerosing pancreatitis", "Autoimmune pancreatitis type 1 (disorder)", "Type 1 IgG4 related autoimmune pancreatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune pancreatitis type 1", "shortest_name_length": 10}
{"curie": "UMLS:C4524805", "names": ["stage IVA gastric cancer", "Stage IVA Gastric (Stomach) Cancer", "Clinical Stage IVA Gastric Cancer AJCC v8", "clinical stage IVA gastric cancer AJCC v8", "clinical stage IVA gastric carcinoma AJCC v8", "Clinical Stage IVA Gastric Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage IVA Gastric Cancer AJCC v8", "shortest_name_length": 24}
{"curie": "UMLS:C5206591", "names": ["Paratesticular Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paratesticular Squamous Cell Carcinoma", "shortest_name_length": 38}
{"curie": "MONDO:0002351", "names": ["glottis cancer", "cancer of glottis", "Ca larynx - glottis", "Neoplasm malig;glottis", "malignant glottis tumor", "Malignant Glottis Tumor", "malignant glottis neoplasm", "malignant glottal neoplasm", "Malignant Tumor of Glottis", "malignant tumor of glottis", "Malignant Glottis Neoplasm", "Malignant tumor of glottis", "Malignant tumour of glottis", "Malignant Neoplasm of Glottis", "malignant neoplasm of glottis", "Malignant neoplasm of glottis", "malignant tumor of the Glottis", "malignant tumor of the glottis", "Malignant Tumor of the Glottis", "malignant neoplasm of the glottis", "Malignant Neoplasm of the Glottis", "malignant neosplasm of the glottis", "Malignant tumor of glottis (disorder)", "malignant neoplasm of glottis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glottis cancer", "shortest_name_length": 14}
{"curie": "UMLS:C5420189", "names": ["Malignant Laryngeal Soft Tissue Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Laryngeal Soft Tissue Neoplasm", "shortest_name_length": 40}
{"curie": "MONDO:0014737", "names": ["DHS2", "xerocytosis Gardos", "XEROCYTOSIS GARDOS", "Desiccytosis Gardos", "desiccytosis Gardos", "DESICCYTOSIS GARDOS", "dehydrated hereditary stomatocytosis 2", "DEHYDRATED HEREDITARY STOMATOCYTOSIS 2", "Dehydrated hereditary stomatocytosis 2", "KCNN4 dehydrated hereditary stomatocytosis", "Dehydrated hereditary stomatocytosis type 2", "dehydrated hereditary stomatocytosis 2; DHS2", "dehydrated hereditary stomatocytosis caused by mutation in KCNN4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dehydrated hereditary stomatocytosis 2", "shortest_name_length": 4}
{"curie": "MONDO:0020523", "names": ["familial parathyroid adenoma", "PARATHYROID ADENOMA, FAMILIAL", "Parathyroid Adenoma, Familial", "hereditary parathyroid gland adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial parathyroid adenoma", "shortest_name_length": 28}
{"curie": "MONDO:0041052", "names": ["PHN", "phn", "Postzoster neuralgia", "post-zoster neuralgia", "Post-zoster neuralgia", "Postherpetic neuralgia", "neuralgia postherpetic", "postherpetic neuralgia", "NEURALGIA POSTHERPETIC", "Postherpetic Neuralgia", "Post-herpetic Neuralgia", "Neuralgia;post-herpetic", "Post-herpetic neuralgia", "POST HERPETIC NEURALGIA", "herpetic neuralgia post", "post-herpetic neuralgia", "Post-Herpetic Neuralgia", "post herpetic neuralgia", "Post herpetic neuralgia", "neuralgias postherpetic", "Neuralgia, Postherpetic", "PHN - Post-herpetic neuralgia", "PHN - post-herpetic neuralgia", "postherpetic neuralgia (etiology)", "Postherpetic neuralgia (disorder)", "postherpetic neuralgia (diagnosis)", "postherpetic; neuralgia (etiology)", "neuralgia; postherpetic (etiology)", "postherpetic neuralgia (manifestation)", "postherpetic; neuralgia (manifestation)", "neuralgia; postherpetic (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postherpetic neuralgia", "shortest_name_length": 3}
{"curie": "MONDO:0005173", "names": ["keratosis", "Keratosis", "Keratosis NOS", "solar keratosis", "Solar keratosis", "Solar Keratosis", "Senile keratoma", "keratoma; senile", "Senile Keratosis", "senile keratosis", "Senile keratosis", "senile; keratoma", "Actinic Keratoses", "ACTINIC KERATOSIS", "Actinic keratosis", "Actinic Keratosis", "KERATOSIS ACTINIC", "Actinic keratoses", "actinic keratosis", "keratosis; senile", "senile; keratosis", "Keratosis, Actinic", "Atrophic keratosis", "KERATOSIS, ACTINIC", "Keratosis, actinic", "keratosis, actinic", "keratosis actinica", "Keratoses, Actinic", "actinic; keratosis", "keratosis; actinic", "sunshine; keratosis", "keratosis; sunshine", "SK - Solar keratosis", "Solar hyperkeratosis", "SK - solar keratosis", "solar hyperkeratosis", "actinic porokeratosis", "Senile hyperkeratosis", "Senile Hyperkeratosis", "Actinic porokeratosis", "hyperkeratosis; senile", "senile; hyperkeratosis", "AK - Actinic keratosis", "SENILE SOLAR KERATOSIS", "Hyperplastic keratosis", "actinic (solar) keratosis", "actinic (Solar) Keratosis", "Actinic (Solar) Keratosis", "actinic keratosis (disease)", "Actinic keratosis (disorder)", "actinic keratosis (diagnosis)", "Keratinocytic intraepidermal neoplasia", "Actinic keratosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "actinic keratosis", "shortest_name_length": 9}
{"curie": "MONDO:0007666", "names": ["glaucoma sleep apnea", "glaucoma and sleep apnea", "Glaucoma and Sleep Apnea", "GLAUCOMA AND SLEEP APNEA", "glaucoma-sleep apnea syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glaucoma-sleep apnea syndrome", "shortest_name_length": 20}
{"curie": "UMLS:C2698294", "names": ["BCLU", "HGBL, NOS", "High-Grade B-Cell Lymphoma, NOS", "High Grade B-Cell Lymphoma, NOS", "High Grade B-Cell Lymphoma, Not Otherwise Specified", "High-Grade B-Cell Lymphoma, Not Otherwise Specified", "B-cell lymphoma unclassifiable with features intermediate between Burkitt lymphoma and diffuse large B-cell lymphoma", "B-cell lymphoma, unclassifiable, with features intermediate between diffuse large B-cell lymphoma and Burkitt lymphoma", "B-Cell Lymphoma, Unclassifiable, with Features Intermediate between Diffuse Large B-Cell Lymphoma and Burkitt Lymphoma", "B-cell lymphoma unclassifiable with features intermediate between Burkitt lymphoma and diffuse large B-cell lymphoma (diagnosis)", "B-cell lymphoma, unclassifiable, with features intermediate between diffuse large B-cell lymphoma and Burkitt lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade B-Cell Lymphoma, Not Otherwise Specified", "shortest_name_length": 4}
{"curie": "MONDO:0008183", "names": ["Anular pancreas", "anular pancreas", "Annular Pancreas", "annular pancreas", "Annular pancreas", "pancreas annular", "pancreas, annular", "PANCREAS, ANNULAR", "Pancreas, annular", "annular; pancreas", "pancreas; annular", "pancreas; annulare", "annulare; pancreas", "Annular pancreas (disorder)", "annular pancreas (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "annular pancreas", "shortest_name_length": 15}
{"curie": "MONDO:0002789", "names": ["hemangiopericytic tumor", "Hemangiopericytic Tumor", "Hemangiopericytic Neoplasm", "Hemangiopericytic neoplasm", "hemangiopericytic neoplasm", "Haemangiopericytic neoplasms", "[M]Haemangiopericytic neoplasms"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemangiopericytic tumor", "shortest_name_length": 23}
{"curie": "UMLS:C0751595", "names": ["Juvenile Pyruvate Dehydrogenase Complex Deficiency Disease", "Pyruvate Dehydrogenase Complex Deficiency Disease, Juvenile"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Juvenile Pyruvate Dehydrogenase Complex Deficiency Disease", "shortest_name_length": 58}
{"curie": "MONDO:0004987", "names": ["bladder tumor", "Bladder tumor", "Bladder Tumor", "tumor bladder", "bladder tumors", "Tumor, Bladder", "Bladder Tumors", "Bladder tumour", "Bladder cancer", "Tumors, Bladder", "Bladder--Tumors", "Bladder neoplasm", "Neoplasm bladder", "tumor of bladder", "Tumor of Bladder", "bladder neoplasm", "BLADDER NEOPLASM", "Bladder Neoplasm", "NEOPLASM BLADDER", "Neoplasm, Bladder", "Bladder neoplasms", "bladder neoplasms", "Bladder Neoplasms", "Neoplasms, Bladder", "neoplasm of bladder", "Neoplasm of Bladder", "Neoplasm of bladder", "Tumor of the Bladder", "Bladder neoplasm NOS", "tumor of the bladder", "Urinary Bladder Tumor", "urinary bladder tumor", "Urinary Bladder Tumors", "urinary bladder tumors", "neoplasm of the bladder", "Neoplasm of the Bladder", "NEOPLASM URINARY BLADDER", "Tumor of Urinary Bladder", "Neoplasm urinary bladder", "Tumor of urinary bladder", "Urinary Bladder Neoplasm", "urinary bladder neoplasm", "tumor of urinary bladder", "bladder neoplasm urinary", "Urinary Bladder Neoplasms", "urinary bladder neoplasms", "Tumour of urinary bladder", "Neoplasm, Urinary Bladder", "Neoplasm of Urinary Bladder", "NGB - New growth of bladder", "neoplasm of urinary bladder", "Tumor of the Urinary Bladder", "tumor of the urinary bladder", "Neoplasm of bladder (disorder)", "neoplasm of the urinary bladder", "Neoplasm of the Urinary Bladder", "neoplasm of bladder (diagnosis)", "urinary bladder neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urinary bladder neoplasm", "shortest_name_length": 13}
{"curie": "UMLS:C0684968", "names": ["Benign Pyriform Sinus Tumor", "Benign Pyriform Fossa Tumor", "Benign tumor of pyriform sinus", "Benign Tumor of Pyriform Sinus", "Benign Pyriform Fossa Neoplasm", "Benign Tumor of Pyriform Fossa", "Benign tumor of pyriform fossa", "Benign Pyriform Sinus Neoplasm", "Benign tumour of pyriform fossa", "Benign tumour of pyriform sinus", "Benign Neoplasm of Pyriform Sinus", "Benign neoplasm of pyriform sinus", "Benign Neoplasm of Pyriform Fossa", "Benign neoplasm of pyriform fossa", "Benign Tumor of the Pyriform Sinus", "Benign Tumor of the Pyriform Fossa", "Benign Neoplasm of the Pyriform Fossa", "Benign Neoplasm of the Pyriform Sinus", "Benign neoplasm of pyriform sinus (disorder)", "benign tumor of pyriform sinus of hypopharynx", "benign neoplasm of pyriform sinus of hypopharynx", "benign neoplasm of pyriform sinus of hypopharynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign neoplasm of pyriform sinus", "shortest_name_length": 27}
{"curie": "MONDO:0004079", "names": ["Lung Polyadenoma", "lung polyadenoma", "Bronchial Cystadenoma", "bronchial cystadenoma", "Lung Mucous Gland Adenoma", "lung mucous gland adenoma", "bronchial mucus gland adenoma", "Bronchial mucous gland adenoma", "adenoma of bronchial mucus gland", "adenoma of bronchial mucous gland", "Adenoma of bronchial mucous gland", "Adenoma of Bronchial Mucous Gland", "adenoma of the Bronchial Mucus gland", "adenoma of the bronchial mucus gland", "adenoma of the bronchial mucous gland", "Adenoma of the Bronchial Mucous Gland", "Adenoma of bronchial mucous gland (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung mucous gland adenoma", "shortest_name_length": 16}
{"curie": "MONDO:0041775", "names": ["IFIS", "Intraoperative floppy iris syndrome", "intraoperative floppy iris syndrome", "IFIS - intraoperative floppy iris syndrome", "Intraoperative floppy iris syndrome (IFIS)", "Intraoperative floppy iris syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intraoperative floppy iris syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0002586", "names": ["Thymic tumor", "thymic tumor", "Thymus Cancer", "thymic cancer", "thymus cancer", "Thymic Cancer", "cancer thymus", "Thymus cancer", "Thymus Cancers", "Thymus--Cancer", "Thymic Cancers", "Cancer, Thymus", "Cancer, Thymic", "thymic neoplasm", "Cancers, Thymic", "Cancers, Thymus", "cancer of thymus", "cancer of Thymus", "Cancer of Thymus", "of thymus cancer", "neoplasm of thymus", "Cancer of the Thymus", "cancer of the Thymus", "Malignant Thymus Tumor", "malignant Thymus tumor", "malignant Thymus neoplasm", "malignant thymus neoplasm", "Malignant Thymus Neoplasm", "malignant tumor of Thymus", "Malignant Tumor of Thymus", "Malignant tumor of thymus", "Malignant tumour of thymus", "malignant neoplasm of Thymus", "Malignant Neoplasm of Thymus", "malignant neoplasm of thymus", "Malignant neoplasm of thymus", "malignant tumor of the Thymus", "Malignant Tumor of the Thymus", "Malignant Neoplasm of the Thymus", "malignant neoplasm of the Thymus", "Malignant tumor of thymus (disorder)", "malignant neoplasm of thymus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thymus cancer", "shortest_name_length": 12}
{"curie": "MONDO:0032844", "names": ["ILFS3", "infantile liver failure syndrome 3", "INFANTILE LIVER FAILURE SYNDROME 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile liver failure syndrome 3", "shortest_name_length": 5}
{"curie": "UMLS:C5205967", "names": ["Seminal Vesicle Mammary-Type Myofibroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Seminal Vesicle Mammary-Type Myofibroblastoma", "shortest_name_length": 45}
{"curie": "MONDO:0002761", "names": ["Cervical Verrucous Carcinoma", "cervical verrucous carcinoma", "uterine cervix verrucous carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical verrucous carcinoma", "shortest_name_length": 28}
{"curie": "UMLS:C0346996", "names": ["metastasis to the cervix", "Metastasis to the Cervix", "Cancer metastatic to cervix", "Secondary cancer of the cervix", "Metastasis to the Cervix Uteri", "Metastasis to the Uterine Cervix", "cervical malignant neoplasm secondary", "secondary malignant neoplasm of cervix", "Metastatic Malignant Tumor to the Cervix", "metastasis of malignant neoplasm to cervix", "Metastatic Malignant Neoplasm to the Cervix", "Secondary malignant neoplasm of cervix uteri", "Metastatic malignant neoplasm of cervix uteri", "Metastatic malignant neoplasm to cervix uteri", "Secondary malignant neoplasm of uterine cervix", "Metastatic malignant neoplasm to uterine cervix", "Metastatic Malignant Tumor to the Uterine Cervix", "secondary malignant neoplasm of cervix (diagnosis)", "Metastatic Malignant Neoplasm in the Uterine Cervix", "Metastatic Malignant Neoplasm to the Uterine Cervix", "metastasis of malignant neoplasm to cervix (diagnosis)", "Metastatic malignant neoplasm to cervix uteri (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Malignant Neoplasm to the Cervix", "shortest_name_length": 24}
{"curie": "MONDO:0018637", "names": ["familial chylomicronemia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial chylomicronemia syndrome", "shortest_name_length": 33}
{"curie": "UMLS:C4759840", "names": ["neurosensory deafness", "Deafness neurosensory", "Deafness Neurosensory", "Deafness, neurosensory"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Deafness Neurosensory", "shortest_name_length": 21}
{"curie": "MONDO:0003681", "names": ["MYCHS", "Myxoid chondrosarcoma", "myxoid chondrosarcoma", "Myxoid Chondrosarcoma", "Myxoid chondrosarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myxoid chondrosarcoma", "shortest_name_length": 5}
{"curie": "MONDO:0011460", "names": ["ARVC6", "ARVD6", "arrhythmogenic right ventricular dysplasia 6", "ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 6", "arrhythmogenic right ventricular dysplasia type 6", "arrhythmogenic right ventricular cardiomyopathy 6", "Arrhythmogenic Right Ventricular Cardiomyopathy 6", "familial arrhythmogenic right ventricular dysplasia 6", "Arrhythmogenic Right Ventricular Dysplasia, Familial, 6", "ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 6", "arrhythmogenic right ventricular dysplasia, familial, 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arrhythmogenic right ventricular dysplasia 6", "shortest_name_length": 5}
{"curie": "MONDO:0100196", "names": ["TPM2 myopathy", "TPM2-related myopathy", "congenital myopathy related to TPM2", "autosomal dominant TPM2-related myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "TPM2-related myopathy", "shortest_name_length": 13}
{"curie": "UMLS:C4763504", "names": ["Adrenal Gland Ganglioneuroblastoma, Nodular"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adrenal Gland Ganglioneuroblastoma, Nodular", "shortest_name_length": 43}
{"curie": "UMLS:C5419402", "names": ["Intervertebral Disc Compression or Protrusion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intervertebral Disc Compression or Protrusion", "shortest_name_length": 45}
{"curie": "MONDO:0060490", "names": ["NMIHBA", "PRUNE1-related neurological syndrome", "Prune exopolyphosphatase 1-related neurological syndrome", "Prune exopolyphosphatase 1-related neurological syndrome (disorder)", "neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies", "NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies", "shortest_name_length": 6}
{"curie": "MONDO:0031481", "names": ["MEDS", "MEDS1", "microcephaly, epilepsy, and diabetes syndrome", "MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME", "MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME 1", "microcephaly, epilepsy, and diabetes syndrome 1", "primary microcephaly-epilepsy-permanent neonatal diabetes syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly, epilepsy, and diabetes syndrome 1", "shortest_name_length": 4}
{"curie": "UMLS:C1332474", "names": ["Benign Atrial Tumor", "Benign Atrial Neoplasm", "Benign Tumor of Cardiac Atrium", "Benign Tumor of Atrium of Heart", "Benign Neoplasm of Cardiac Atrium", "Benign Tumor of the Cardiac Atrium", "Benign Neoplasm of Atrium of Heart", "Benign Neoplasm of the Cardiac Atrium", "Benign Tumor of the Atrium of the Heart", "Benign Neoplasm of the Atrium of the Heart"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Atrial Neoplasm", "shortest_name_length": 19}
{"curie": "MONDO:0014574", "names": ["PLACK", "plack", "PLACK syndrome", "plack syndrome", "peeling skin-leukonychia-acral punctate keratoses-cheilitis-knuckle pads syndrome", "peeling skin-leukonuchia-acral punctate keratoses-cheilitis-knuckle pads syndrome", "Peeling skin-leukonychia-acral punctate keratoses-cheilitis-knuckle pads syndrome", "PEELING SKIN WITH LEUKONYCHIA, ACRAL PUNCTATE KERATOSES, CHEILITIS, AND KNUCKLE PADS", "peeling skin with leukonychia, acral punctate keratoses, cheilitis, and knuckle pads", "Peeling skin, leuconychia, acral punctate keratoses, cheilitis, knuckle pads syndrome", "Peeling skin, leukonychia, acral punctate keratoses, cheilitis, knuckle pads syndrome", "PLACK (peeling skin, leukonychia, acral punctate keratoses, cheilitis, knuckle pads) syndrome", "Peeling skin, leukonychia, acral punctate keratoses, cheilitis, knuckle pads syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peeling skin-leukonuchia-acral punctate keratoses-cheilitis-knuckle pads syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0235245", "names": ["psychogenic syncope", "Psychogenic syncope", "Psychogenic Syncope", "SYNCOPE, PSYCHOGENIC", "Psychogenic syncope (disorder)", "psychogenic syncope (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Psychogenic syncope", "shortest_name_length": 19}
{"curie": "MONDO:0014111", "names": ["CTRCT19", "cataract 19", "cataract type 19", "cataract 19 multiple types", "cataract 19, multiple types", "CATARACT 19, MULTIPLE TYPES", "LIM2 early-onset non-syndromic cataract", "early-onset non-syndromic cataract caused by mutation in LIM2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 19 multiple types", "shortest_name_length": 7}
{"curie": "MONDO:0004049", "names": ["shellshock", "shell shock", "Shell shock", "Shell Shock", "Shock, Shell", "war neurosis", "shell Shocks", "Shell Shocks", "shells shock", "war neuroses", "shock, shell", "neurosis, war", "neuroses, war", "Shocks, Shell", "Shocks, shell", "disorder combat", "Combat Neurosis", "combat neurosis", "combat disorder", "Combat Neuroses", "combat neuroses", "Combat neurosis", "Combat Disorder", "Neuroses, Combat", "Neurosis, Combat", "neurosis, combat", "Disorder, Combat", "combat disorders", "Combat Disorders", "neuroses, combat", "disorder, combat", "Disorders, Combat", "state; shellshock", "disorders, combat", "shellshock; state", "Shell shock (disorder)", "combat stress disorder", "shell shock (diagnosis)", "combat stress disorders", "disorder, combat stress", "stress disorder, combat", "stress disorders, combat", "disorders, combat stress"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combat disorder", "shortest_name_length": 10}
{"curie": "UMLS:C0334331", "names": ["reninoma", "Reninoma", "Reninoma syndrome", "Juxtaglomerular Tumor", "Juxtaglomerular tumor", "tumor; juxtaglomerular", "Juxtaglomerular tumour", "juxtaglomerular; tumor", "[M]Juxtaglomerular tumor", "Juxtaglomerular Neoplasm", "[M]Juxtaglomerular tumour", "Juxtaglomerular Cell Tumor", "juxta-glomerular cell tumor", "Juxtaglomerular tumor (disorder)", "juxta-glomerular cell tumor of kidney", "Juxtaglomerular tumor (morphologic abnormality)", "juxta-glomerular cell tumor of kidney (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Juxtaglomerular tumor", "shortest_name_length": 8}
{"curie": "MONDO:0012182", "names": ["SKELETAL DYSPLASIA, RHIZOMELIC, WITH RETINITIS PIGMENTOSA", "skeletal dysplasia, rhizomelic, with retinitis pigmentosa", "Skeletal Dysplasia, Rhizomelic, with Retinitis Pigmentosa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skeletal dysplasia, rhizomelic, with retinitis pigmentosa", "shortest_name_length": 57}
{"curie": "UMLS:C0085648", "names": ["ganglion", "myxoid cyst", "Synovial Cyst", "Synovial cyst", "Cyst;synovial", "synovial cyst", "ganglion cyst", "synovial; cyst", "synovial cysts", "Cyst, Synovial", "Synovial cysts", "Synovial Cysts", "cyst; synovial", "Cysts, Synovial", "Synovial cyst NOS", "Synovial cyst, NOS", "Synovial cyst (disorder)", "synovial cyst (diagnosis)", "Synovial cyst, unspecified", "Synovial cyst (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Synovial Cyst", "shortest_name_length": 8}
{"curie": "MONDO:0013379", "names": ["NS7", "NOONAN SYNDROME 7", "Noonan syndrome 7", "Noonan Syndrome 7", "BRAF Noonan syndrome", "Noonan syndrome type 7", "Noonan syndrome caused by mutation in BRAF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Noonan syndrome 7", "shortest_name_length": 3}
{"curie": "UMLS:C0749948", "names": ["URINARY STRAIN", "Urinary Straining", "Urinary straining"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urinary straining", "shortest_name_length": 14}
{"curie": "MONDO:0002836", "names": ["UCU", "Urethral Urothelial Cancer", "urethral urothelial cancer", "Urothelial carcinoma urethra", "Urethral Urothelial Carcinoma", "urethral urothelial carcinoma", "urethra transitional cell carcinoma", "Urethra Transitional Cell Carcinoma", "Transitional cell carcinoma urethra", "Urethral Transitional Cell Carcinoma", "urethral transitional cell carcinoma", "transitional cell carcinoma of urethra", "Transitional Cell Carcinoma of Urethra", "transitional cell carcinoma of the urethra", "Transitional Cell Carcinoma of the Urethra", "transitional cell carcinoma of urethra (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urethra transitional cell carcinoma", "shortest_name_length": 3}
{"curie": "MONDO:0009756", "names": ["NPD-A", "sphingomyelin lipidosis", "Sphingomyelin Lipidosis", "Sphingomyelin Lipidoses", "SPHINGOMYELIN LIPIDOSIS", "Lipidosis, Sphingomyelin", "ASMD, NEUROVISCERAL TYPE", "Lipidoses, Sphingomyelin", "niemann-pick disease type", "Niemann-Pick disease type A", "sphingomyelinase deficiency", "Sphingomyelinase Deficiency", "Type A Niemann Pick Disease", "SPHINGOMYELINASE DEFICIENCY", "niemann-pick disease type a", "Type A Niemann-Pick Disease", "Niemann-Pick Disease, Type A", "Deficiency, Sphingomyelinase", "Infantile neurovisceral ASMD", "NIEMANN-PICK DISEASE, TYPE A", "Niemann-Pick disease, type A", "Niemann Pick Disease, Type A", "Niemann-PICK disease, type A", "Niemann-Pick's Disease Type A", "Sphingomyelinase Deficiencies", "Niemann Pick's Disease Type A", "Classical Niemann-Pick Disease", "Classical Niemann Pick Disease", "Deficiencies, Sphingomyelinase", "Neuronal Cholesterol Lipidosis", "Neuronal Cholesterol Lipidoses", "Classical Niemann-Pick disease", "Lipidosis, Neuronal Cholesterol", "Cholesterol Lipidosis, Neuronal", "Cholesterol Lipidoses, Neuronal", "Niemann-Pick Disease, Classical", "Lipidoses, Neuronal Cholesterol", "Sphingomyelin Cholesterol Lipidosis", "Sphingomyelin Cholesterol Lipidoses", "Supraoptic Vertical Ophthalmoplegia", "Sphingomyelinase Deficiency Disease", "Cholesterol Lipidoses, Sphingomyelin", "Ophthalmoplegia, Supraoptic Vertical", "Supraoptic Vertical Ophthalmoplegias", "Vertical Ophthalmoplegia, Supraoptic", "Lipidosis, Sphingomyelin Cholesterol", "Sphingomyelinase Deficiency Diseases", "Cholesterol Lipidosis, Sphingomyelin", "Lipidoses, Sphingomyelin Cholesterol", "Vertical Ophthalmoplegias, Supraoptic", "Niemann-Pick disease neuropathic type", "Ophthalmoplegias, Supraoptic Vertical", "Niemann-Pick disease type A (diagnosis)", "Niemann-Pick disease, type A (disorder)", "Niemann-Pick Disease, Neuronopathic Type", "Niemann Pick Disease, Neuronopathic Type", "Niemann-Pick disease, acute neuropathic form", "Niemann Pick Disease, Acute Neurovisceral Form", "Niemann-Pick disease, acute neurovisceral form", "Niemann-Pick Disease, Acute Neuronopathic Form", "Niemann Pick Disease, Acute Neuronopathic Form", "Niemann-Pick Disease, Acute Neurovisceral Form", "ACID SPHINGOMYELINASE DEFICIENCY, NEUROVISCERAL TYPE", "Infantile neurovisceral acid sphingomyelinase deficiency", "NIEMANN-PICK DISEASE, INTERMEDIATE, PROTRACTED NEUROVISCERAL", "Niemann-Pick disease, Intermediate, protracted neurovisceral", "Niemann-Pick Disease, Intermediate, Protracted Neurovisceral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Niemann-Pick disease type A", "shortest_name_length": 5}
{"curie": "MONDO:0008111", "names": ["ODDD", "ODOD", "ODD SYNDROME", "ODD syndrome", "odd syndrome", "ODD Syndrome", "ODDD syndrome", "curtius syndrome", "Curtius' syndrome", "Curtius' syndrome I", "oculodentodigital syndrome", "Oculodentodigital syndrome", "syndrome oculodentodigital", "Oculodentodigital Syndrome", "Oculodentoosseous Dysplasia", "oculodentoosseous dysplasia", "oculodentodigital dysplasia", "Meyer-Schwickerath syndrome", "Oculodentodigital Dysplasia", "OCULODENTODIGITAL DYSPLASIA", "Oculodentoosseous dysplasia", "OCULODENTOOSSEOUS DYSPLASIA", "Oculodentodigital dysplasia", "Meyer-Schwinkerath syndrome", "Oculo-dento-digital syndrome", "oculodentodigital; dysplasia", "oculo-dento-digital syndrome", "oculo dento digital syndrome", "dysplasia; oculodentodigital", "oculo-dento-osseous dysplasia", "dysplasia oculodentodigitalis", "dento-oculo-osseous dysplasia", "oculo-dento-digital dysplasia", "Oculo-Dento-Osseous Dysplasia", "Oculo-Dento-Digital Dysplasia", "osseous-oculo-dental dysplasia", "Osseous-Oculo-Dental Dysplasia", "oculo-dento-digital (ODD) syndrome", "oculo-dento-osseous dysplasia (ODOD)", "OCULODENTODIGITAL DYSPLASIA SYNDROME", "Oculodentodigital syndrome (disorder)", "Meyer-Schwinkerath and Weyers syndrome", "oculo-dento-digital (ODD) dysplasia (ODDD)", "Ectodermal dysplasia-ocular malformation syndrome", "Ectodermal dysplasia with ocular malformations syndrome", "Ectodermal dysplasia-ocular malformation syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculodentodigital dysplasia", "shortest_name_length": 4}
{"curie": "MONDO:0016882", "names": ["partial deletion of chromosome 20", "partial monosomy of chromosome 20", "partial deletion of chromosome type 20"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of chromosome 20", "shortest_name_length": 33}
{"curie": "UMLS:C0392115", "names": ["Uninhibited Neurogenic Bladder", "Uninhibited neurogenic bladder", "Neurogenic Bladder, Uninhibited", "bladder; neurogenic, uninhibited", "Neurogenic Urinary Bladder, Uninhibited", "Uninhibited neurogenic bladder (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neurogenic Urinary Bladder, Uninhibited", "shortest_name_length": 30}
{"curie": "UMLS:C0393791", "names": ["Congenital facial nerve palsy", "Congenital Facial Nerve Palsy", "Congenital facial nerve palsy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital facial nerve palsy", "shortest_name_length": 29}
{"curie": "UMLS:C1334177", "names": ["Invasive cervical cancer", "invasive cervical cancer", "cancer cervical invasive", "Infiltrating Cervical Cancer", "Infiltrating Cervical Carcinoma", "Cancer of uterine cervix, invasive", "invasive carcinoma of uterine cervix", "Carcinoma of uterine cervix, invasive", "cervical malignant carcinoma uterine, invasive", "Carcinoma of uterine cervix, invasive (disorder)", "invasive carcinoma of uterine cervix (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infiltrating Cervical Carcinoma", "shortest_name_length": 24}
{"curie": "UMLS:C3898146", "names": ["Neonatal Spell", "Neonatal Spells"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neonatal Spell", "shortest_name_length": 14}
{"curie": "MONDO:0002036", "names": ["Penis Disease", "penis disease", "disease penis", "Disorder penis", "Penis Diseases", "PENIS DISORDER", "DISORDER PENIS", "penile disease", "diseases penis", "penis disorder", "disorder penis", "penis diseases", "Penile Disease", "Disease, Penis", "Penis disorder", "Penile Disorder", "Diseases, Penis", "penile diseases", "Penis--Diseases", "Disease, Penile", "Penis Disorders", "disorders penis", "penis disorders", "penile disorder", "Penile Diseases", "disease of penis", "Penile Disorders", "Penile disorders", "Diseases, Penile", "penile disorders", "disorder of penis", "Disorder of penis", "Disorders of penis", "Penile disorder NOS", "diseases of the penis", "Disease of penis, NOS", "DISEASES OF THE PENIS", "Disorder of penis, NOS", "penis disease or disorder", "disease or disorder of penis", "disease (or disorder); penis", "Disorder of penis (disorder)", "disorder of penis (diagnosis)", "Unspecified disorder of penis", "Disorder of penis, unspecified", "Other specified disorders of penis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "penile disorder", "shortest_name_length": 13}
{"curie": "UMLS:C0017667", "names": ["nodular glomerulosclerosis", "Nodular glomerulosclerosis", "nodular glomerulosclerosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nodular glomerulosclerosis", "shortest_name_length": 26}
{"curie": "MONDO:0005138", "names": ["lung cancer", "Lung Cancer", "cancer of lung", "Carcinoma;lung", "Carcinoma lung", "CARCINOMA LUNG", "Lung Carcinoma", "Cancer of Lung", "carcinoma lung", "lung carcinoma", "LUNG CARCINOMA", "Lung carcinoma", "carcinomas lung", "carcinoma lungs", "Lung cancer, NOS", "lung cancer, NOS", "Carcinoma of Lung", "CARCINOMA OF LUNG", "carcinoma of lung", "Carcinoma of lung", "of lung carcinoma", "Cancer of the Lung", "cancer of the lung", "pulmonary carcinoma", "Pulmonary carcinoma", "PULMONARY CARCINOMA", "carcinoma of the lung", "Carcinoma;respiratory", "Carcinoma of the Lung", "Lung Cancer (all types)", "carcinoma of lung (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung carcinoma", "shortest_name_length": 11}
{"curie": "UMLS:C3273078", "names": ["Liver Yolk Sac Tumor", "Hepatic Yolk Sac Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liver Yolk Sac Tumor", "shortest_name_length": 20}
{"curie": "MONDO:0011406", "names": ["congenital cholesteatoma", "Congenital cholesteatoma", "cholesteatoma, congenital", "Cholesteatoma, Congenital", "CHOLESTEATOMA, CONGENITAL", "Congenital cholesteatoma (disorder)", "congenital cholesteatoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholesteatoma, congenital", "shortest_name_length": 24}
{"curie": "MONDO:0016655", "names": ["Del(6)(p22)", "Monosomy 6p22", "monosomy 6p22", "6p22 microdeletion syndrome", "6p22 microdeletion syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "6p22 microdeletion syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0000407", "names": ["malignant pleural solitary fibrous tumor", "pleural solitary fibrous tumor, malignant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant pleural solitary fibrous tumor", "shortest_name_length": 40}
{"curie": "UMLS:C0039978", "names": ["disease thoracic", "Thoracic Disease", "thoracic disease", "Thoracic Disorder", "Disease, Thoracic", "thoracic disorder", "Thoracic Diseases", "thoracic diseases", "Diseases, Thoracic", "Disorder of thorax", "thoracic disorder (diagnosis)", "Disorder of thorax (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thoracic Diseases", "shortest_name_length": 16}
{"curie": "UMLS:C3203532", "names": ["Infected dermal cyst"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infected dermal cyst", "shortest_name_length": 20}
{"curie": "MONDO:0700101", "names": ["carcinoma, non-human animal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma, non-human animal", "shortest_name_length": 27}
{"curie": "MONDO:0004665", "names": ["NSHD", "NSHL", "NSCHL", "nodular sclerosis", "Hodgkin; nodular sclerosis", "Hodgkin's Nodular Sclerosis", "Hodgkin's nodular sclerosis", "Nodular sclerosis Hodgkin lymphoma", "Nodular Sclerosis Hodgkin Lymphoma", "Hodgkin disease, nodular sclerosis", "LYMPHOMA HODGKIN NODULAR SCLEROSIS", "nodular sclerosis Hodgkin lymphoma", "Nodular Sclerosis Hodgkin's Disease", "Hodgkin's disease nodular sclerosis", "nodular sclerosis Hodgkin's disease", "Hodgkin lymphoma, nodular sclerosis", "nodular sclerosis Hodgkin's lymphoma", "Nodular Sclerosis Hodgkin's Lymphoma", "Hodgkin's disease, nodular sclerosis", "Hodgkin's lymphoma, nodular sclerosis", "disease; Hodgkin's, nodular sclerosis", "Hodgkin's disease nodular sclerosis NOS", "Hodgkin disease, nodular sclerosis, NOS", "Hodgkin's disease with nodular sclerosis", "Hodgkin Lymphoma, Nodular Sclerosis, NOS", "Hodgkin's disease, nodular sclerosis NOS", "Hodgkin's disease, nodular sclerosis, NOS", "nodular sclerosis Classic Hodgkin lymphoma", "Nodular Sclerosis Classic Hodgkin Lymphoma", "nodular sclerosis classical Hodgkin lymphoma", "Nodular Sclerosis Classical Hodgkin Lymphoma", "Nodular sclerosis classical Hodgkin lymphoma", "Classical Hodgkin lymphoma, nodular sclerosis", "classical Hodgkin lymphoma, nodular sclerosis", "nodular sclerosis Hodgkin lymphoma (diagnosis)", "Hodgkin's disease, nodular sclerosis (disorder)", "Hodgkin's disease, nodular sclerosis (clinical)", "Classic Hodgkin lymphoma, nodular sclerosis type", "Classical Hodgkin lymphoma, nodular sclerosis, NOS", "Hodgkin's disease nodular sclerosis stage unspecified", "Hodgkin's disease, nodular sclerosis of unspecified site", "Hodgkin lymphoma, nodular sclerosis (morphologic abnormality)", "Hodgkin's disease, nodular sclerosis NOS (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nodular sclerosis classical Hodgkin lymphoma", "shortest_name_length": 4}
{"curie": "MONDO:0007966", "names": ["susceptibility to uveal melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "susceptibility to uveal melanoma", "shortest_name_length": 32}
{"curie": "UMLS:C0274861", "names": ["Inorganic Arsenic Poisoning", "Inorganic arsenic poisoning", "Poisoning, Inorganic Arsenic", "Inorganic Arsenic Poisonings", "Arsenic Poisoning, Inorganic", "Poisonings, Inorganic Arsenic", "Arsenic Poisonings, Inorganic", "Inorganic arsenic poisoning (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arsenic Poisoning, Inorganic", "shortest_name_length": 27}
{"curie": "MONDO:0016377", "names": ["PTHSL", "Pitt-Hopkins-like syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pitt-Hopkins-like syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C3273066", "names": ["BAF", "Biliary Adenofibroma", "Intrahepatic Bile Duct Adenofibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Biliary Adenofibroma", "shortest_name_length": 3}
{"curie": "MONDO:0015643", "names": ["PSE", "photic epilepsy", "Photic epilepsy", "photogenic epilepsy", "television epilepsy", "Television epilepsy", "Photogenic epilepsy", "Epilepsy, Photogenic", "Photosensitive epilepsy", "Photosensitive Epilepsy", "photosensitive epilepsy", "photoparoxysmal response", "Epilepsy, Photosensitive", "Photosensitive Epilepsies", "Epilepsies, Photosensitive", "Pure photosensitive epilepsy", "Photogenic epilepsy (disorder)", "Photosensitive Reflex Epilepsy", "Epilepsy, Photosensitive Reflex", "Reflex Epilepsy, Photosensitive", "Photosensitive Reflex Epilepsies", "Reflex Epilepsies, Photosensitive", "Epilepsies, Photosensitive Reflex", "Epilepsy only in relation to photic stimulation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "photosensitive epilepsy", "shortest_name_length": 3}
{"curie": "MONDO:0009057", "names": ["cyanosis and hepatic disease", "CYANOSIS AND HEPATIC DISEASE", "Cyanosis and Hepatic Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cyanosis and hepatic disease", "shortest_name_length": 28}
{"curie": "UMLS:C1511260", "names": ["Borderline Ovarian Clear Cell Cystadenofibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Ovarian Clear Cell Cystadenofibroma", "shortest_name_length": 46}
{"curie": "UMLS:C0678202", "names": ["regional enteritis", "REGIONAL ENTERITIS", "Enteritis;regional", "Regional enteritis", "Enteritis, Regional", "ENTERITIS, REGIONAL", "Regional enteritis NOS", "granulomatous enteritis", "Granulomatous enteritis", "Granulomatous Enteritis", "RE - Regional enteritis", "Enteritis, Granulomatous", "bowel; regional enteritis", "Crohn's regional enteritis", "regional enteritis (diagnosis)", "Granulomatous enteritis (disorder)", "Regional enteritis of unspecified site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Regional enteritis", "shortest_name_length": 18}
{"curie": "UMLS:C0349615", "names": ["Suprasellar Germ Cell Tumor", "germ cell tumor suprasellar", "Suprasellar germ cell tumor", "Suprasellar germ cell tumour", "Suprasellar germ cell tumor (disorder)", "Suprasellar germ cell tumor (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Suprasellar germ cell tumor", "shortest_name_length": 27}
{"curie": "UMLS:C0280305", "names": ["Upper Gum SCC", "SCC of Upper Gum", "Upper Gingival SCC", "SCC of the Upper Gum", "SCC of Upper Gingiva", "SCC of the Upper Gingiva", "Upper Gum Squamous Cell Carcinoma", "Squamous Cell Carcinoma of Upper Gum", "Upper Gingival Squamous Cell Carcinoma", "Squamous Cell Carcinoma of the Upper Gum", "Squamous Cell Carcinoma of Upper Gingiva", "Squamous Cell Carcinoma of the Upper Gingiva"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Upper Gingival Squamous Cell Carcinoma", "shortest_name_length": 13}
{"curie": "MONDO:0020717", "names": ["ADWH", "autosomal dominant woolly hair", "woolly hair, autosomal dominant", "WOOLLY HAIR, AUTOSOMAL DOMINANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant woolly hair", "shortest_name_length": 4}
{"curie": "MONDO:0004481", "names": ["Intraductal papillary-mucinous carcinoma, invasive", "pancreatic invasive intraductal papillary-mucinous carcinoma", "Pancreatic Invasive Intraductal Papillary-Mucinous Carcinoma", "Invasive intraductal papillary-mucinous carcinoma of pancreas", "invasive intraductal papillary-mucinous carcinoma of pancreas", "Malignant intraductal papillary-mucinous carcinoma of pancreas", "Invasive intraductal papillary-mucinous carcinoma of pancreas (disorder)", "invasive intraductal papillary-mucinous carcinoma of pancreas (diagnosis)", "Intraductal papillary mucinous neoplasm with an associated invasive carcinoma", "Pancreatic Intraductal Papillary-Mucinous Neoplasm with an Associated Invasive Carcinoma", "pancreatic intraductal papillary mucinous neoplasm with an associated invasive carcinoma", "Pancreatic Intraductal Papillary Mucinous Neoplasm with an Associated Invasive Carcinoma", "pancreatic intraductal papillary-mucinous neoplasm with an associated invasive carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic intraductal papillary-mucinous neoplasm with an associated invasive carcinoma", "shortest_name_length": 50}
{"curie": "MONDO:0013476", "names": ["CMH19", "hypertrophic cardiomyopathy 19", "CALR3 hypertrophic cardiomyopathy", "hypertrophic cardiomyopathy type 19", "cardiomyopathy familial hypertrophic 19", "cardiomyopathy, familial hypertrophic, 19", "cardiomyopathy, familial hypertrophic, type 19", "hypertrophic cardiomyopathy caused by mutation in CALR3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophic cardiomyopathy 19", "shortest_name_length": 5}
{"curie": "MONDO:0009299", "names": ["XXGD", "ODG1", "XX-GD", "FSH-RO", "ovarian dysgenesis", "OVARIAN DYSGENESIS 1", "XX gonadal dysgenesis", "XX GONADAL DYSGENESIS", "46 XX gonadal dysgenesis", "46,XX Ovarian Dysgenesis", "46,XX ovarian dysgenesis", "46,XX gonadal dysgenesis", "46,XX Gonadal Dysgenesis", "Gonadal Dysgenesis, 46,XX", "Gonadal Dysgenesis, 46, XX", "Gonadal Dysgenesis, XX Type", "GONADAL DYSGENESIS, XX TYPE", "XX female gonadal dysgenesis", "Pure gonadal dysgenesis 46,XX", "46,XX pure gonadal dysgenesis", "Pure Gonadal Dysgenesis, 46,XX", "Pure Gonadal Dysgenesis, 46, XX", "46,XX complete gonadal dysgenesis", "OVARIAN FAILURE, HYPERGONADOTROPIC", "Hypergonadotropic ovarian dysgenesis", "hypergonadotropic ovarian dysgenesis", "Pure gonadal dysgenesis 46,XX (disorder)", "Ovarian dysgenesis with normal chromosomes", "follicular stimulating hormone-resistant ovaries", "Follicular stimulating hormone-resistant ovaries", "OVARIAN DYSGENESIS, HYPERGONADOTROPIC, AUTOSOMAL RECESSIVE", "OVARIAN DYSGENESIS, HYPERGONADOTROPIC, WITH NORMAL KARYOTYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46 XX gonadal dysgenesis", "shortest_name_length": 4}
{"curie": "MONDO:0008092", "names": ["neutrophilia hereditary", "hereditary neutrophilia", "Hereditary neutrophilia", "Neutrophilia, Hereditary", "neutrophilia, hereditary", "NEUTROPHILIA, HEREDITARY", "Hereditary neutrophilia (disorder)", "Hereditary neutrophilia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary neutrophilia", "shortest_name_length": 23}
{"curie": "MONDO:0011985", "names": ["HIGM4", "hyper IgM syndrome 4", "Hyper-Igm Syndrome 4", "HYPER-IgM SYNDROME 4", "hyper-IgM syndrome 4", "Hyper-IgM syndrome type 4", "hyper-IgM syndrome type 4", "immunodeficiency with hyper-IgM type 4", "immunodeficiency with hyper IgM type 4", "IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 4", "Immunodeficiency With Hyper-Igm, Type 4", "immunodeficiency with hyper-IgM, type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyper-IgM syndrome type 4", "shortest_name_length": 5}
{"curie": "MONDO:0013573", "names": ["CED3", "CRANIOECTODERMAL DYSPLASIA 3", "CRANIOECTODERMAL dysplasia 3", "cranioectodermal dysplasia 3", "IFT43 cranioectodermal dysplasia", "Cranioectodermal dysplasia type 3", "cranioectodermal dysplasia caused by mutation in IFT43"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cranioectodermal dysplasia 3", "shortest_name_length": 4}
{"curie": "MONDO:0017885", "names": ["CRCC", "ChRCC", "CHRCC", "kidney chromophobe", "chromophobe carcinoma", "Chromophobe carcinoma", "Chromophobe Carcinoma", "Chromophobe adenocarcinoma", "chromophobe adenocarcinoma", "Chromophobe Adenocarcinoma", "chromophobe renal cell cancer", "Chromophobe Renal Cell Cancer", "chromophobe carcinoma of kidney", "Chromophobe Carcinoma of Kidney", "Chromophobe carcinoma of kidney", "Chromophobe Renal Cell Carcinoma", "Chromophobe cell renal carcinoma", "Chromophobe renal cell carcinoma", "chromophobe renal cell carcinoma", "RENAL CELL CARCINOMA, CHROMOPHOBE", "Chromophobe Carcinoma of the Kidney", "chromophobe carcinoma of the kidney", "chromophobe cell carcinoma of kidney", "Chromophobe Cell Carcinoma of Kidney", "chromophobe renal cell adenocarcinoma", "chromophobe type renal cell carcinoma", "Chromophobe renal cell adenocarcinoma", "Renal cell carcinoma, chromophobe cell", "Renal Cell Carcinoma, Chromophobe Type", "renal cell carcinoma, chromophobe type", "renal cell carcinoma, chromophobe cell", "Renal cell carcinoma, chromophobe type", "Chromophobe Cell Carcinoma of the Kidney", "chromophobe cell carcinoma of the kidney", "Chromophobe renal cell carcinoma (disorder)", "Chromophobe renal cell carcinoma (diagnosis)", "Chromophobe carcinoma (morphologic abnormality)", "chromophobe type renal cell carcinoma (diagnosis)", "Renal cell carcinoma, chromophobe cell (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromophobe renal cell carcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0013283", "names": ["CVID3", "common variable immunodeficiency 3", "immunodeficiency, common variable, 3", "IMMUNODEFICIENCY, COMMON VARIABLE, 3", "ANTIBODY DEFICIENCY DUE TO CD19 DEFECT", "antibody deficiency due to CD19 defect", "Antibody Deficiency due to Defect in CD19", "immunodeficiency, common variable, type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency, common variable, 3", "shortest_name_length": 5}
{"curie": "MONDO:0003607", "names": ["forelimb neuritis", "neuritis of forelimb", "neuritis of upper limb", "mononeuritis of upper limb and mononeuritis multiplex", "Mononeuritis of upper limb and mononeuritis multiplex"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuritis of upper limb", "shortest_name_length": 17}
{"curie": "MONDO:0001095", "names": ["mediastinal neuroblastoma", "mediastinum neuroblastoma", "Mediastinal Neuroblastoma", "neuroblastoma of mediastinum", "Neuroblastoma of Mediastinum", "neuroblastoma of the mediastinum", "Neuroblastoma of the Mediastinum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mediastinum neuroblastoma", "shortest_name_length": 25}
{"curie": "MONDO:0007827", "names": ["IBM", "Ibm", "sIBM", "inflammatory myopathy", "INCLUSION BODY MYOSITIS", "body inclusion myositis", "myositis inclusion body", "Inclusion Body Myositis", "inclusion body myositis", "Inclusion body myositis", "Myositis, Inclusion Body", "Inclusion Body Myositides", "bodies inclusion myositis", "Myositides, Inclusion Body", "IBM - Inclusion body myositis", "Inclusion body myositis [IBM]", "sporadic inclusion body myositis", "Sporadic inclusion body myositis", "Inclusion body myositis (disorder)", "inclusion body myositis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inclusion body myositis", "shortest_name_length": 3}
{"curie": "MONDO:0015787", "names": ["symptomatic form of hemophilia A in female carriers"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "symptomatic form of hemophilia A in female carriers", "shortest_name_length": 51}
{"curie": "UMLS:C0151241", "names": ["ATRIAL MYXOMA", "atrial myxoma", "Atrial myxoma", "Atrial Myxoma", "atrial myxomas", "Myxoma of Atrium", "Myxoma of the Atrium", "Atrial myxoma (disorder)", "Atrial myxoma (diagnosis)", "benign cardiac neoplasm atrial myxoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atrial myxoma", "shortest_name_length": 13}
{"curie": "UMLS:C0520562", "names": ["Intestinal dilatation", "INTESTINAL DILATATION", "Intestinal loop dilated", "Dilatation of intestine", "Intestinal dilatation, NOS", "Dilatation of intestine, NOS", "Dilatation of intestine (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dilatation of intestine", "shortest_name_length": 21}
{"curie": "MONDO:0017968", "names": ["46,XY ovotesticular DSD", "46,XY ovotesticular disorder of sex development", "46,XY ovotesticular disorder of sex development (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XY ovotesticular disorder of sex development", "shortest_name_length": 23}
{"curie": "MONDO:0019329", "names": ["capillary lymphangioma", "microcystic lymphangioma", "superficial lymphangioma", "capillary lymphatic malformation", "superficial lymphatic malformation", "microcystic lymphatic malformation", "cutaneous lymphangioma circumscriptum", "microcystic infiltrating lymphatic malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcystic lymphatic malformation", "shortest_name_length": 22}
{"curie": "MONDO:0012624", "names": ["MC1DN20", "ACAD9 deficiency", "ACAD9 DEFICIENCY", "ACYL-CoA DEHYDROGENASE 9 DEFICIENCY", "acyl-CoA dehydrogenase 9 deficiency", "Acyl-CoA dehydrogenase 9 deficiency", "ACAD9 (acyl-CoA dehydrogenase 9) deficiency", "Deficiency of acyl-coenzyme A dehydrogenase 9", "nuclear type mitochondrial complex I deficiency 20", "mitochondrial complex I deficiency, nuclear type 20", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20", "Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of", "mitochondrial complex I deficiency due to ACAD9 deficiency", "MITOCHONDRIAL COMPLEX I DEFICIENCY DUE TO ACAD9 DEFICIENCY", "mitochondrial complex 1 deficiency due to ACAD9 deficiency", "Mitochondrial complex I deficiency due to deficiency of acyl-coenzyme A dehydrogenase 9", "Mitochondrial complex I deficiency due to deficiency of acyl-coenzyme A dehydrogenase 9 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acyl-CoA dehydrogenase 9 deficiency", "shortest_name_length": 7}
{"curie": "MONDO:0024359", "names": ["central sleep apnea due to periodic breathing", "Central sleep apnea due to periodic breathing", "Central sleep apnoea due to periodic breathing", "Central sleep apnea due to periodic breathing (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central sleep apnea due to periodic breathing", "shortest_name_length": 45}
{"curie": "UMLS:C3275115", "names": ["No Cardiac Valve Regurgitation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "No Cardiac Valve Regurgitation", "shortest_name_length": 30}
{"curie": "UMLS:C0744869", "names": ["Metastatic liver cell carcinoma", "HEPATOCELLULAR CARCINOMA METASTATIC", "Metastatic Hepatocellular Carcinoma", "Hepatocellular carcinoma metastatic", "Metastatic hepatocellular carcinoma", "Metastatic hepatocellular carcinoma (disorder)", "Metastatic hepatocellular carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic hepatocellular carcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C4526729", "names": ["Refractory Erdheim-Chester Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Erdheim-Chester Disease", "shortest_name_length": 34}
{"curie": "UMLS:C3274455", "names": ["Acquired Rickets"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired Rickets", "shortest_name_length": 16}
{"curie": "UMLS:C1335461", "names": ["Stage I Hepatoblastoma", "Postsurgical Stage I Hepatoblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postsurgical Stage I Hepatoblastoma", "shortest_name_length": 22}
{"curie": "UMLS:C0206044", "names": ["Calicivirus Infection", "Infection, Calicivirus", "Calicivirus Infections", "Infections, Calicivirus", "Disease due to Calicivirus", "DISEASES DUE TO CALICIVIRUS", "Disease caused by Calicivirus", "Disease due to Calicivirus, NOS", "Disease caused by Calicivirus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infections, Calicivirus", "shortest_name_length": 21}
{"curie": "UMLS:C2931074", "names": ["Cone rod dystrophy amelogenesis imperfecta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cone rod dystrophy amelogenesis imperfecta", "shortest_name_length": 42}
{"curie": "UMLS:C0340670", "names": ["Radiation damage to artery", "Radiation-Induced Damage to Artery", "Radiation damage to artery (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radiation damage to artery", "shortest_name_length": 26}
{"curie": "UMLS:C5418266", "names": ["Non-Communicable Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Communicable Disorder", "shortest_name_length": 25}
{"curie": "UMLS:C5237193", "names": ["Advanced Pancreatic Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Pancreatic Carcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0012028", "names": ["AIS3", "VAMAS4", "AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 3", "autoimmune disease, susceptibility to, 3", "AUTOIMMUNE DISEASE SUSCEPTIBILITY LOCUS, CHROMOSOME 8-RELATED", "autoimmune disease susceptibility locus, chromosome 8-related", "VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 4", "vitiligo-associated multiple autoimmune disease susceptibility 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune disease, susceptibility to, 3", "shortest_name_length": 4}
{"curie": "MONDO:0033547", "names": ["LIGOWS", "Li-Ghorgani-Weisz-Hubshman syndrome", "LI-GHORBANI-WEISZ-HUBSHMAN SYNDROME", "Li-Ghorbani-Weisz-Hubshman syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Li-Ghorbani-Weisz-Hubshman syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0007571", "names": ["SFNP", "PERYTHM", "Primary Erythermalgia", "Primary erythermalgia", "primary erythermalgia", "small fiber neuropathy", "Erythermalgia, Primary", "Primary Erythermalgias", "Small Fibre Neuropathy", "ERYTHERMALGIA, PRIMARY", "Small fibre neuropathy", "erythermalgia, primary", "Small Fiber Neuropathy", "Small fiber neuropathy", "Erythromelalgia Type II", "primary erythromelalgia", "Erythermalgias, Primary", "neuropathy, small fiber", "Neuropathy, Small Fiber", "Neuropathy, Small Fibre", "Primary Erythromelalgia", "NEUROPATHY, SMALL FIBER", "Primary erythromelalgia", "ERYTHROMELALGIA, PRIMARY", "Erythromelalgia, Primary", "Small Fibre Neuropathies", "erythromelalgia, primary", "Small Fiber Neuropathies", "Familial Erythromelalgia", "Erythromelalgia, primary", "ERYTHROMELALGIA, FAMILIAL", "erythromelalgia, familial", "Neuropathies, Small Fibre", "Neuropathies, Small Fiber", "Erythromelalgia, Familial", "Mitchell disease (formerly)", "Small Nerve Fiber Neuropathy", "Small nerve fiber neuropathy", "SFNP - Small fiber neuropathy", "Small fiber neuropathy (disorder)", "Primary erythromelalgia (disorder)", "small fiber neuropathy (diagnosis)", "Painful Peripheral Neuropathy Small Nerve Fiber Neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary erythermalgia", "shortest_name_length": 4}
{"curie": "MONDO:0015152", "names": ["Limb-girdle muscular dystrophy autosomal recessive", "Autosomal recessive limb-girdle muscular dystrophy", "autosomal recessive limb-girdle muscular dystrophy", "limb-girdle muscular dystrophy, autosomal recessive", "muscular dystrophy, limb-girdle, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive limb-girdle muscular dystrophy", "shortest_name_length": 50}
{"curie": "MONDO:0017392", "names": ["PDCD", "Pre-descemet corneal dystrophy", "pre-descemet corneal dystrophy", "Pre-Descemet corneal dystrophy", "Pre-Descemet's corneal dystrophy", "corneal dystrophy Pre-Descemet's", "Pre-descemet's corneal dystrophy", "Pre-descemet's corneal dystrophy (disorder)", "Pre-Descemet's corneal dystrophy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pre-descemet corneal dystrophy", "shortest_name_length": 4}
{"curie": "UMLS:C5237209", "names": ["Hereditary Colorectal Cancer Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hereditary Colorectal Cancer Syndrome", "shortest_name_length": 37}
{"curie": "UMLS:C4527181", "names": ["Stage IIA", "Stage IIA Cutaneous (Skin) Melanoma", "Pathologic Stage IIA Cutaneous Melanoma AJCC v8", "Pathologic Stage IIA Melanoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IIA Cutaneous Melanoma AJCC v8", "shortest_name_length": 9}
{"curie": "UMLS:C1148522", "names": ["Acoustic Trauma", "Trauma;acoustic", "ACOUSTIC TRAUMA", "Acoustic trauma", "acoustic trauma", "trauma; acoustic", "acoustic; trauma", "DEAFNESS, CHRONIC ACOUSTIC TRAUMA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acoustic Trauma", "shortest_name_length": 15}
{"curie": "MONDO:0011035", "names": ["NFNS", "Noonan-Neurofibromatosis Syndrome", "NEUROFIBROMATOSIS-NOONAN SYNDROME", "Noonan-neurofibromatosis syndrome", "NOONAN-NEUROFIBROMATOSIS SYNDROME", "Neurofibromatosis Noonan syndrome", "neurofibromatosis-Noonan syndrome", "Noonan neurofibromatosis syndrome", "Neurofibromatosis-Noonan syndrome", "Neurofibromatosis with Noonan phenotype", "NEUROFIBROMATOSIS WITH NOONAN PHENOTYPE", "neurofibromatosis with Noonan phenotype", "Neurofibromatosis type 1-Noonan syndrome", "Neurofibromatosis type 1 Noonan syndrome", "NFNS - Neurofibromatosis Noonan syndrome", "neurofibromatosis type 1-Noonan syndrome", "Neurofibromatosis Noonan syndrome (disorder)", "neurofibromatosis-Noonan syndrome (NFNS, NF-NS)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurofibromatosis-Noonan syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0007949", "names": ["MRSHS", "marshall syndrome", "Marshall syndrome", "MARSHALL SYNDROME", "Marshall Syndrome", "marshalls syndrome", "Marshall's syndrome", "marshall's syndrome", "Marshall syndrome (disorder)", "deafness, myopia, cataract, saddle nose-Marshall type", "Deafness, myopia, cataract, saddle nose-Marshall type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Marshall syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C5554549", "names": ["Recurrent Cervical Adenocarcinoma, Usual-Type", "Recurrent Cervical Adenocarcinoma, Usual Type", "Recurrent Endocervical Adenocarcinoma, Usual Type", "Recurrent Endocervical Adenocarcinoma, Usual-Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Endocervical Adenocarcinoma, Usual-Type", "shortest_name_length": 45}
{"curie": "UMLS:C1335467", "names": ["Precancerous Dermatitis", "precancerous dermatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Precancerous Dermatitis", "shortest_name_length": 23}
{"curie": "UMLS:C4727152", "names": ["Refractory Hemophagocytic Lymphohistiocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Hemophagocytic Lymphohistiocytosis", "shortest_name_length": 45}
{"curie": "UMLS:C0339350", "names": ["lens; anomaly", "anomaly; lens", "Congenital lens anomaly", "Congenital Lens Disorder", "Lens disorders congenital", "Congenital anomaly of lens", "deformity; lens, congenital", "Congenital lens anomaly NOS", "lens; deformity, congenital", "Lens abnormality, congenital", "Congenital lens malformations", "congenital lens malformations", "Congenital malformation of lens", "Congenital anomaly of lens (disorder)", "Congenital lens malformation, unspecified", "congenital lens malformations (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital anomaly of lens", "shortest_name_length": 13}
{"curie": "UMLS:C4525298", "names": ["Stage I Gallbladder Cancer", "Stage I Gallbladder Cancer AJCC v8", "Stage I Gallbladder Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Gallbladder Cancer AJCC v8", "shortest_name_length": 26}
{"curie": "MONDO:0014976", "names": ["COXPD31", "combined oxidative phosphorylation deficiency 31", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 31", "MIPEP combined oxidative phosphorylation deficiency", "combined oxidative phosphorylation deficiency type 31", "combined oxidative phosphorylation deficiency caused by mutation in MIPEP", "lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome", "shortest_name_length": 7}
{"curie": "MONDO:0012486", "names": ["PREAURICULAR TAG, ISOLATED, AUTOSOMAL DOMINANT, 1", "preauricular tag, isolated, autosomal dominant, 1", "Preauricular Tag, Isolated, Autosomal Dominant, 1", "preauricular Tag, isolated, autosomal dominant, type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "preauricular tag, isolated, autosomal dominant, 1", "shortest_name_length": 49}
{"curie": "UMLS:C1333864", "names": ["Grade II PIN", "Grade II Prostatic Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade II Prostatic Intraepithelial Neoplasia", "shortest_name_length": 12}
{"curie": "MONDO:0013754", "names": ["ARCL1B", "cutis laxa type IB", "cutis laxa type IB (diagnosis)", "autosomal recessive cutis laxa type IB", "cutis laxa, autosomal recessive, type 1B", "CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB", "cutis laxa, autosomal recessive, type IB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutis laxa, autosomal recessive, type 1B", "shortest_name_length": 6}
{"curie": "UMLS:C2987139", "names": ["Pancreatic Well Differentiated Ductal Adenocarcinoma", "Pancreatic Well-Differentiated Ductal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Well Differentiated Ductal Adenocarcinoma", "shortest_name_length": 52}
{"curie": "MONDO:0008730", "names": ["Adrenal Hyperplasia V", "adrenal hyperplasia 5", "ADRENAL HYPERPLASIA V", "17a-hydroxylase deficiency", "CAH - 17-hydroxylase deficiency", "17 alpha-hydroxylase deficiency", "17 alpha-Hydroxylase deficiency", "17-ALPHA-HYDROXYLASE DEFICIENCY", "17-Alpha-Hydroxylase deficiency", "17-alpha-hydroxylase deficiency", "17,20-Lyase Deficiency, Isolated", "17,20-lyase deficiency, isolated", "17,20-LYASE DEFICIENCY, ISOLATED", "17,20-@LYASE DEFICIENCY, ISOLATED", "congenital adrenal hyperplasia type 5", "Congenital adrenal hyperplasia, type 5", "Adrenal hyperplasia, congenital, type 5", "Steroid 17 alpha-monooxygenase deficiency", "Steroid 17-alpha-monooxygenase deficiency", "Deficiency of steroid 17-alpha-hydroxylase", "CAH due to 17-alpha-hydroxylase deficiency", "17 alpha-hydroxylase deficiency (diagnosis)", "17-alpha-hydroxylase/17,20-lyase deficiency", "Deficiency of steroid 17-alpha-monooxygenase", "combined 17-hydroxylase/17,20-lyase deficiency", "Combined 17-hydroxylase/17,20-lyase deficiency", "CAH - 17-alpha-hydroxysteroid dehydrogenase deficiency", "Deficiency of steroid 17-alpha-monooxygenase (disorder)", "17-Alpha-Hydroxylase-17,20-Lyase Deficiency, Combined Partial", "Adrenogenital disorder due to 17 alpha-hydroxylase deficiency", "17-ALPHA-HYDROXYLASE/17,20-LYASE DEFICIENCY, COMBINED PARTIAL", "Adrenogenital disorder due to 17-alpha-hydroxylase deficiency", "17-Alpha-Hydroxylase/17,20-lyase deficiency, combined partial", "17-ALPHA-HYDROXYLASE/17,20-LYASE DEFICIENCY, COMBINED COMPLETE", "17-Alpha-Hydroxylase/17,20-lyase deficiency, combined complete", "17-Alpha-Hydroxylase-17,20-Lyase Deficiency, Combined Complete", "Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency", "congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency", "Adrenal hyperplasia, congenital due to 17-alpha-hydroxylase deficiency", "Adrenal Hyperplasia, Congenital, Due To 17-Alpha-Hydroxylase Deficiency", "ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 17-ALPHA-HYDROXYLASE DEFICIENCY", "adrenal hyperplasia, congenital, due to 17-ALPHA-HYDROXYLASE deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency", "shortest_name_length": 21}
{"curie": "MONDO:0100137", "names": ["STS", "Telomere Disease", "Telomere Syndrome", "telomere syndrome", "short telomere syndrome", "Telomere Biology Disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "telomere syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C4331955", "names": ["Stage IVC Major Salivary Gland Cancer", "Stage IVC Major Salivary Gland Cancer AJCC v8", "Stage IVC Major Salivary Gland Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Major Salivary Gland Cancer AJCC v8", "shortest_name_length": 37}
{"curie": "UMLS:C0028798", "names": ["Occupational Exposure", "Occupational exposure", "exposure occupational", "OCCUPATIONAL EXPOSURE", "occupational exposure", "EXPOSURE OCCUPATIONAL", "Occupational exposures", "occupational exposures", "exposures occupational", "Occupational Exposures", "Exposure, Occupational", "Exposures, Occupational"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Occupational Exposure", "shortest_name_length": 21}
{"curie": "MONDO:0000748", "names": ["Mastoiditis", "MASTOIDITIS", "mastoiditis", "Mastoiditides", "Mastoid empyema", "Mastoiditis NOS", "mastoid; empyema", "empyema; mastoid", "Mastoiditis, NOS", "Empyema of mastoid", "mastoiditis (disease)", "Mastoiditis (disorder)", "mastoiditis (diagnosis)", "Unspecified mastoiditis", "mastoid disorder empyema", "Mastoiditis, unspecified", "Empyema of mastoid (disorder)", "Empyema of mastoid (diagnosis)", "mastoid process of temporal boneitis", "Unspecified mastoiditis, unspecified ear", "mastoid process of temporal bone inflammation", "inflammation of mastoid process of temporal bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mastoiditis", "shortest_name_length": 11}
{"curie": "UMLS:C5204983", "names": ["Refractory EBV-Related Lymphoma", "Refractory EBV-Associated Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory EBV-Related Lymphoma", "shortest_name_length": 31}
{"curie": "MONDO:0007355", "names": ["COB1", "Coloboma-microphthalmos syndrome", "coloboma-microphthalmos syndrome", "coloboma cleft lip/palate-mental retardation syndrome", "coloboma-cleft lip/palate-mental retardation syndrome", "coloboma, cleft lip/palate and mental retardation syndrome", "Coloboma, cleft lip-palate and mental retardation syndrome", "Uveal coloboma-cleft lip-palate-mental retardation syndrome", "Uveal coloboma-cleft lip/palate-mental retardation syndrome", "uveal coloboma-cleft lip and palate-intellectual disability", "uveal coloboma-cleft lip/palate-mental retardation syndrome", "coloboma, cleft lip/palate and intellectual disability syndrome", "uveal coloboma-cleft lip/palate-intellectual disability syndrome", "coloboma-microphthalmos-hearing loss-hematuria-cleft lip/palate syndrome", "ocular coloboma with or without hearing impairment, cleft lip/palate, and/or mental retardation", "coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or mental retardation", "COLOBOMA, OCULAR, WITH OR WITHOUT HEARING IMPAIRMENT, CLEFT LIP/PALATE, AND/OR MENTAL RETARDATION", "coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or intellectual disability", "Coloboma-microphthalmos syndrome associated with sensorineural hearing loss, hematuria, and cleft lip-palate", "coloboma-microphthalmos syndrome associated with sensorineural hearing loss, hematuria, and cleft lip/palate", "COLOBOMA, OCULAR, WITH OR WITHOUT HEARING IMPAIRMENT, CLEFT LIP/PALATE, AND/OR IMPAIRED INTELLECTUAL DEVELOPMENT", "COLOBOMA, OCULAR, WITH OR WITHOUT HEARING IMPAIRMENT, CLEFT LIP/PALATE, AND/OR INTELLECTUAL DEVELOPMENTAL DISORDER"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uveal coloboma-cleft lip and palate-intellectual disability", "shortest_name_length": 4}
{"curie": "UMLS:C5555546", "names": ["Myxoid Glioneuronal Tumor of the Septum Pellucidum", "Myxoid Glioneuronal Tumor, PDGFRA p.K385-Mutant of the Septum Pellucidum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myxoid Glioneuronal Tumor of the Septum Pellucidum", "shortest_name_length": 50}
{"curie": "UMLS:C4331954", "names": ["Stage IV Major Salivary Gland Cancer", "Stage IV Major Salivary Gland Cancer AJCC v8", "Stage IV Major Salivary Gland Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Major Salivary Gland Cancer AJCC v8", "shortest_name_length": 36}
{"curie": "MONDO:0006804", "names": ["IBC", "mastitis Carcinomatosa", "Mastitis carcinomatosa", "Inflammatory carcinoma", "Mastitis Carcinomatosa", "mastitis carcinomatosa", "breast cancer inflammatory", "Inflammatory Breast Cancer", "breast inflammatory cancer", "inflammatory breast cancer", "inflammatory cancer breast", "Inflammatory breast cancer", "Cancer, Inflammatory Breast", "Breast Cancer, Inflammatory", "Inflammatory Breast Cancers", "breast cancer, inflammatory", "Cancers, Inflammatory Breast", "Inflammatory Breast Neoplasm", "Breast Cancers, Inflammatory", "Inflammatory breast carcinoma", "inflammatory carcinoma breast", "inflammatory breast carcinoma", "Breast carcinoma inflammatory", "Inflammatory Breast Carcinoma", "breast inflammatory carcinoma", "Neoplasm, Inflammatory Breast", "Breast Neoplasm, Inflammatory", "Inflammatory Breast Neoplasms", "Breast Inflammatory Carcinoma", "Breast Neoplasms, Inflammatory", "Carcinoma, Inflammatory Breast", "Inflammatory Breast Carcinomas", "Neoplasms, Inflammatory Breast", "Breast Carcinoma, Inflammatory", "Carcinomas, Inflammatory Breast", "Breast Carcinomas, Inflammatory", "Inflammatory Breast Cancer (IBC)", "Inflammatory Carcinoma of Breast", "inflammatory carcinoma of breast", "Inflammatory carcinoma of breast", "Inflammatory Carcinoma of the Breast", "inflammatory carcinoma of the breast", "Inflammatory carcinoma of the breast", "carcinoma of the breast, inflammatory", "Inflammatory carcinoma of breast (disorder)", "inflammatory carcinoma of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory breast carcinoma", "shortest_name_length": 3}
{"curie": "MONDO:0005033", "names": ["GN", "Gangliocytoma", "gangliocytoma", "Gangliocytomas", "ganglioneuroma", "Ganglioneuroma", "gangliocytomas", "GANGLIONEUROMA", "ganglioneuromas", "Ganglioneuromas", "GANGLIONEUROFIBROMA", "Mature Ganglioneuroma", "GANGLIONEUROMA, BENIGN", "ganglioneuroma, benign", "ganglioneuroma (disease)", "Ganglioneuroma (disorder)", "neural Crest tumor, benign", "Neural Crest Tumor, Benign", "Gangliocytoma (morphologic abnormality)", "Ganglioneuroma (morphologic abnormality)", "ganglioneuroma (Schwannian Stroma-dominant)", "Ganglioneuroma (Schwannian Stroma-Dominant)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ganglioneuroma", "shortest_name_length": 2}
{"curie": "MONDO:0009207", "names": ["factor V and factor VIII, combined deficiency of, with normal protein C and protein C inhibitor", "Factor V And Factor VIII, Combined Deficiency Of, With Normal Protein C And Protein C Inhibitor", "factor 5 and Factor VIII, combined deficiency Of, with normal Protein C and Protein C inhibitor", "FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, WITH NORMAL PROTEIN C AND PROTEIN C INHIBITOR", "factor V and Factor VIII, combined deficiency of, with normal protein c and Protein C inhibitor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "factor V and factor VIII, combined deficiency of, with normal protein C and protein C inhibitor", "shortest_name_length": 95}
{"curie": "MONDO:0004468", "names": ["Anal Canal Paget Disease", "anal canal Paget disease", "Anal Canal Paget's Disease", "anal canal Paget's disease", "Paget disease of anal canal", "Pagets disease of anal canal", "Paget's Disease of Anal Canal", "Paget's disease of anal canal", "Paget Disease of the Anal Canal", "Paget disease of the anal canal", "Paget's Disease of the Anal Canal", "Paget's disease of the anal canal", "anal canal mammary Paget's disease", "Paget disease of anal canal (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anal canal Paget disease", "shortest_name_length": 24}
{"curie": "MONDO:0004660", "names": ["stage 0 lung cancer", "Lung cancer in situ", "Lung cancer stage 0", "Stage 0 Lung Cancer", "Lung carcinoma stage 0", "Cancer in situ of lung", "stage 0 lung carcinoma", "Lung carcinoma in situ", "Cancer of lung in situ", "lung in situ carcinoma", "Stage 0 Lung Carcinoma", "lung carcinoma in situ", "Cancer of lung stage 0", "Carcinoma in situ of lung", "carcinoma in situ of lung", "Carcinoma of lung in situ", "Carcinoma of lung stage 0", "Pulmonary carcinoma stage 0", "Stage 0 Lung Cancer AJCC v6", "Bronchial Carcinoma in situ", "Pulmonary carcinoma in situ", "stage 0 lung cancer aJCC v6", "stage 0 lung cancer aJCC v7", "Stage 0 Lung Cancer AJCC v7", "bronchial carcinoma in situ", "Carcinoma in situ of lung, NOS", "stage 0 lung cancer aJCC v6 and v7", "Stage 0 Lung Cancer AJCC v6 and v7", "Carcinoma in situ of lung (disorder)", "carcinoma in situ of lung (diagnosis)", "carcinoma in situ of bronchus and lung", "Carcinoma in situ of bronchus and lung", "Lung carcinoma cell type unspecified stage 0", "Carcinoma in situ of bronchus and lung (disorder)", "carcinoma in situ of bronchus and lung (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung carcinoma in situ", "shortest_name_length": 19}
{"curie": "UMLS:C4743576", "names": ["Resectable Pleural Malignant Mesothelioma", "Resectable Malignant Pleural Mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Pleural Malignant Mesothelioma", "shortest_name_length": 41}
{"curie": "MONDO:0023246", "names": ["Linear Porokeratosis", "linear porokeratosis", "Linear porokeratosis", "Porokeratosis, Linear", "Zosteriform porokeratosis", "Porokeratosis, linear type", "Linear porokeratosis (disorder)", "Congenital facial linear porokeratosis (type)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "linear porokeratosis", "shortest_name_length": 20}
{"curie": "UMLS:C4329964", "names": ["Factor II Inactivation", "Factor II Inhibitor Present"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Factor II Inactivation", "shortest_name_length": 22}
{"curie": "UMLS:C4054380", "names": ["Infection Associated Nephrotic Syndrome", "Nephrotic Syndrome - Infection Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - Infection Associated", "shortest_name_length": 39}
{"curie": "UMLS:C2987257", "names": ["Intraepithelial Neoplasia in Barrett Esophagus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraepithelial Neoplasia in Barrett Esophagus", "shortest_name_length": 46}
{"curie": "MONDO:0004579", "names": ["retinoschisis", "Retinoschisis", "Retinoschises", "retinoschises", "Schisis of retina", "Retinoschisis NOS", "RS - Retinoschisis", "Retinoschisis, NOS", "Retinoschisis (disorder)", "Unspecified retinoschisis", "retinoschisis (diagnosis)", "Retinoschisis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinoschisis", "shortest_name_length": 13}
{"curie": "MONDO:0008691", "names": ["Hz/Hc", "PAMI syndrome", "zinc, elevated plasma", "ZINC, ELEVATED PLASMA", "ALBUMIN BINDING OF ZINC, ELEVATED", "albumin binding of zinc, elevated", "hyperzincemia, familial Dysalbuminemic", "HYPERZINCEMIA, FAMILIAL DYSALBUMINEMIC", "hyperzincemia and hypercalprotectinemia", "HYPERZINCEMIA AND HYPERCALPROTECTINEMIA", "Hyperzincemia and hypercalprotectinemia", "Hyperzincaemia and hypercalprotectinaemia", "myeloid-related proteinemia inflammatory syndrome", "Hyperzincemia and hypercalprotectinemia (disorder)", "Hyperzincemia and hypercalprotectinemia (diagnosis)", "disorders of zinc metabolism hyperzincemia and hypercalprotectinemia", "PSTPIP1-associated myeloid-related proteinemia inflammatory syndrome", "PSTPIP1-associated myeloid-related proteinaemia inflammatory syndrome", "Recurrent infection, inflammatory syndrome due to zinc metabolism disorder syndrome", "proline-serine-threonine phosphatase-interacting protein associated myeloid-related proteinemia inflammatory syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "zinc, elevated plasma", "shortest_name_length": 5}
{"curie": "MONDO:0015264", "names": ["COP", "BOOP", "boop", "idiopathic BOOP", "organizing pneumonia", "constrictive bronchiolitis", "Primary Organizing Pneumonia", "Primary Organizing Pneumonias", "Pneumonia, Primary Organizing", "Organizing Pneumonia, Primary", "Organizing Pneumonias, Primary", "Cryptogenic Organizing Pneumonia", "Cryptogenic organising pneumonia", "cryptogenic organising pneumonia", "cryptogenic organizing pneumonia", "Cryptogenic organizing pneumonia", "Pneumonia, Cryptogenic Organizing", "Cryptogenic Organizing Pneumonias", "Organizing Pneumonia, Cryptogenic", "Cryptogenic organising pneumonitis", "Cryptogenic organizing pneumonitis", "cryptogenic organizing pneumonitis", "COP - Cryptogenic organising pneumonitis", "COP - Cryptogenic organizing pneumonitis", "Cryptogenic organizing pneumonia (disorder)", "cryptogenic organizing pneumonia (diagnosis)", "bronchiolitis obliterans organized pneumonia", "Bronchiolitis obliterans organising pneumonia", "Bronchiolitis Obliterans Organizing Pneumonia", "Bronchiolitis obliterans organizing pneumonia", "bronchiolitis obliterans organising pneumonia", "bronchiolitis obliterans organizing pneumonia", "Cryptogenic organizing pneumonitis (diagnosis)", "BRONCHIOLITIS OBLITERANS WITH ORGANIZING PNEUMONIA", "Bronchiolitis obliterans with organizing pneumonia", "BOOP Bronchiolitis Obliterans Organizing Pneumonia", "Bronchiolitis obliterans with organising pneumonia", "Bronchiolitis obliterans and organising pneumonitis", "Bronchiolitis obliterans and organizing pneumonitis", "BOOP - Bronchiolitis obliterans organizing pneumonia", "BOOP - Bronchiolitis obliterans organising pneumonia", "bronchiolitis obliterans organizing pneumonia (BOOP)", "bronchiolitis obliterans organized pneumonia (diagnosis)", "idiopathic bronchiolitis obliterans organizing pneumonia", "BOOP - Bronchiolitis obliterans and organising pneumonitis", "BOOP - Bronchiolitis obliterans and organizing pneumonitis", "Bronchiolitis obliterans with usual interstitial pneumonitis", "idiopathic bronchiolitis obliterans with organizing pneumonia", "idiopathic bronchiolitis obliterans with organising pneumonia", "pneumonitis idiopathic nonspecific interstitial cryptogenic organizing"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cryptogenic organizing pneumonia", "shortest_name_length": 3}
{"curie": "MONDO:0016881", "names": ["partial monosomy of chromosome 19", "partial deletion of chromosome 19", "partial deletion of chromosome type 19"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of chromosome 19", "shortest_name_length": 33}
{"curie": "MONDO:0007006", "names": ["neuropathy ulnar", "Ulnar neuropathy", "ulnar neuropathy", "Ulnar Neuropathy", "Neuropathy;ulnar", "Neuropathy, Ulnar", "Ulnar Neuropathies", "ulnar neuropathies", "Neuropathies, Ulnar", "n.ulnaris; disorder", "Ulnar Nerve Disease", "ulnar nerve disorder", "Nerve Disease, Ulnar", "Ulnar Nerve Diseases", "Nerve Diseases, Ulnar", "nerve disorders ulnar", "ulnar nerve mononeuropathy", "Ulnar neuropathy (disorder)", "mononeuropathy of ulnar nerve", "ulnar nerve disorder (diagnosis)", "disease (or disorder); nerve, ulnar", "ulnar neuropathy (disorder) [ambiguous]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ulnar neuropathy", "shortest_name_length": 16}
{"curie": "UMLS:C4525129", "names": ["Stage IVA Colon Cancer", "Stage IVA Colon Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Colon Cancer AJCC v8", "shortest_name_length": 22}
{"curie": "MONDO:0019237", "names": ["disorder of pyridoxine metabolism", "inborn disorder of pyridoxine metabolism", "inborn pyridoxine metabolic process disorder", "inborn error of pyridoxine metabolic process", "rare inborn error of pyridoxine metabolic process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of pyridoxine metabolism", "shortest_name_length": 33}
{"curie": "UMLS:C1332507", "names": ["Extrahepatic Bile Duct Benign Granular Cell Tumor", "Benign Granular Cell Tumor of Extrahepatic Bile Ducts", "Benign Extrahepatic Bile Duct Granular Cell Myoblastoma", "Benign Granular Cell Myoblastoma of Extrahepatic Bile Duct", "Benign Granular Cell Myoblastoma of the Extrahepatic Bile Duct"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extrahepatic Bile Duct Benign Granular Cell Tumor", "shortest_name_length": 49}
{"curie": "MONDO:0007155", "names": ["Arteritis, Familial Granulomatous, with Juvenile Polyarthritis", "ARTERITIS, FAMILIAL GRANULOMATOUS, WITH JUVENILE POLYARTHRITIS", "arteritis, familial granulomatous, with juvenile polyarthritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arteritis, familial granulomatous, with juvenile polyarthritis", "shortest_name_length": 62}
{"curie": "MONDO:0012812", "names": ["DEE4", "EIEE4", "STXBP1-related encephalopathy", "STXBP1 encephalopathy with epilepsy", "STXBP1-related epileptic encephalopathy", "STXBP1-related early-onset encephalopathy", "Early Infantile Epileptic Encephalopathy 4", "early infantile epileptic encephalopathy 4", "Early infantile epileptic encephalopathy 4", "epileptic encephalopathy, early infantile, 4", "Epileptic Encephalopathy, Early Infantile, 4", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 4", "developmental and epileptic encephalopathy 4", "Developmental and Epileptic Encephalopathy 4", "developmental and epileptic encephalopathy, 4", "STXBP1 early infantile epileptic encephalopathy", "epileptic encephalopathy, early infantile, type 4", "Syntaxin binding protein 1 encephalopathy with epilepsy", "STXBP1 (syntaxin binding protein 1) epileptic encephalopathy", "Syntaxin binding protein 1 encephalopathy with epilepsy (disorder)", "early infantile epileptic encephalopathy caused by mutation in STXBP1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 4", "shortest_name_length": 4}
{"curie": "UMLS:C4082305", "names": ["deafmutism", "Deafmutism", "deaf-mutism", "Deaf-Mutism", "Deaf Mutism", "deaf mutism", "Deaf mutism", "deaf; mutism", "mutism; deaf", "Deaf mutism, NOS", "Nonspeaking deaf", "Nonspeaking deaf, NOS", "Deaf mutism (disorder)", "deaf mutism (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Deaf Mutism", "shortest_name_length": 10}
{"curie": "MONDO:0006230", "names": ["Gastric squamous cell carcinoma", "gastric squamous cell carcinoma", "Gastric Squamous Cell Carcinoma", "stomach squamous cell carcinoma", "Squamous cell carcinoma of stomach", "squamous cell carcinoma of stomach", "Squamous Cell Carcinoma of Stomach", "Squamous cell carcinoma of the stomach", "squamous cell carcinoma of the stomach", "gastric (stomach) squamous cell cancer", "Gastric (Stomach) Squamous Cell Cancer", "Squamous Cell Carcinoma of the Stomach", "Squamous cell carcinoma of stomach (disorder)", "squamous cell carcinoma of stomach (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric squamous cell carcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C0404572", "names": ["Anovulatory", "Anovulation", "anovulatory", "Anovular cycle", "Anovular cycles", "Anovulatory cycle", "anovulatory cycle", "Anovulatory Cycle", "ANOVULATORY CYCLE", "anovulatory; cycle", "anovulatory cycles", "period; anovulatory", "Anovulatory (finding)", "Anovulatory infertility", "ovulation; failure or lack of", "failure or lack of; ovulation", "Female infertility of anovulatory origin", "female infertility associated with anovulation", "Female infertility associated with anovulation", "Infertility, female, associated with anovulation", "infertility; female, associated with anovulation", "female; infertility, associated with anovulation", "Female infertility of anovulatory origin (disorder)", "Female infertility associated with anovulatory cycle", "Female infertility associated with anovulation (disorder)", "female infertility associated with anovulation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Female infertility associated with anovulation", "shortest_name_length": 11}
{"curie": "UMLS:C0751117", "names": ["Cryptogenic Tonic-Clonic Epilepsy", "Cryptogenic Tonic Clonic Epilepsy", "Tonic-Clonic Epilepsy, Cryptogenic", "Epilepsy, Cryptogenic Tonic-Clonic", "Epilepsy, Tonic-Clonic, Cryptogenic", "Cryptogenic Tonic-Clonic Epilepsies", "Epilepsies, Cryptogenic Tonic-Clonic", "Tonic-Clonic Epilepsies, Cryptogenic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cryptogenic Tonic-Clonic Epilepsy", "shortest_name_length": 33}
{"curie": "MONDO:0054866", "names": ["SADS", "sudden arrhythmic death syndrome", "sudden arrhythmia death syndrome", "Sudden arrhythmic death syndrome", "Sudden cardiac death due to cardiac arrhythmia", "sudden cardiac death due to cardiac arrhythmia", "Sudden cardiac death due to cardiac arrhythmia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sudden arrhythmia death syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0009671", "names": ["CHUDLEY SYNDROME", "Chudley syndrome", "Chudley Rozdilsky syndrome", "Chudley-Rozdilsky syndrome", "Intellectual disability-myopathy-short stature-endocrine defect syndrome", "intellectual disability-myopathy-short stature-endocrine defect syndrome", "Intellectual disability, myopathy, short stature, endocrine defect syndrome", "intellectual disability, myopathy, short stature, endocrine defect syndrome", "Intellectual disability, myopathy, short stature, endocrine defect syndrome (disorder)", "intellectual disability, myopathy, short stature, endocrine defect syndrome (diagnosis)", "multicore myopathy with mental retardation, short stature, and hypogonadotropic hypogonadism", "MULTICORE MYOPATHY WITH MENTAL RETARDATION, SHORT STATURE, AND HYPOGONADOTROPIC HYPOGONADISM", "multicore myopathy with intellectual disability, short stature, and hypogonadotropic hypogonadism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability-myopathy-short stature-endocrine defect syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0800046", "names": ["THMA", "THMA1", "Thyroid Hormone Metabolism, Abnormal", "thyroid hormone metabolism, abnormal", "thyroid hormone metabolism, abnormal 1", "THYROID HORMONE METABOLISM 1, ABNORMAL", "THYROID HORMONE METABOLISM, ABNORMAL, 1", "short stature-delayed bone age due to thyroid hormone metabolism deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid hormone metabolism, abnormal 1", "shortest_name_length": 4}
{"curie": "MONDO:0015177", "names": ["MAD", "Metaphyseal anadysplasia", "metaphyseal anadysplasia", "Regressive metaphyseal dysplasia", "regressive metaphyseal dysplasia", "Metaphyseal anadysplasia (disorder)", "Maroteaux Verloes Stanescu syndrome", "Maroteaux-Verloes-Stanescu syndrome", "Early-onset regressive form of metaphyseal dysplasia", "early-onset regressive form of metaphyseal dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metaphyseal anadysplasia", "shortest_name_length": 3}
{"curie": "MONDO:0000182", "names": ["CMS-TA", "congenital myasthenic syndrome with tubular aggregates", "myasthenic syndrome, congenital, with tubular aggregates"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myasthenic syndrome with tubular aggregates", "shortest_name_length": 6}
{"curie": "UMLS:C0334363", "names": ["Papillary Mucinous Cystadenoma", "Papillary mucinous cystadenoma", "Papillary mucinous cystadenoma NOS", "Papillary mucinous cystadenoma, NOS", "Papillary Pseudomucinous Cystadenoma", "Papillary pseudomucinous cystadenoma", "Papillary pseudomucinous cystadenoma, NOS", "papillary; cystadenoma, mucinous, unspecified site", "mucinous; cystadenoma, papillary, unspecified site", "cystadenoma; papillary, mucinous, unspecified site", "cystadenoma; mucinous, papillary, unspecified site", "cystadenoma; papillary, pseudomucinous, unspecified site", "pseudomucinous; cystadenoma, papillary, unspecified site", "cystadenoma; pseudomucinous, papillary, unspecified site", "papillary; cystadenoma, pseudomucinous, unspecified site", "Papillary mucinous cystadenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Papillary mucinous cystadenoma", "shortest_name_length": 30}
{"curie": "UMLS:C4683663", "names": ["Marginal Zone Lymphoma by Ann Arbor Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Marginal Zone Lymphoma by Ann Arbor Stage", "shortest_name_length": 41}
{"curie": "MONDO:0004030", "names": ["ureter urothelial cancer", "Ureter Urothelial Cancer", "ureter urothelial carcinoma", "Urothelial carcinoma ureter", "Ureter Urothelial Carcinoma", "Ureter transitional cell cancer", "ureteral Urothelial cell carcinoma", "Ureter Transitional Cell Carcinoma", "ureteral urothelial cell carcinoma", "ureter transitional cell carcinoma", "Transitional cell carcinoma ureter", "Ureteral Urothelial Cell Carcinoma", "Urothelial Cell Carcinoma of Ureter", "urothelial cell carcinoma of ureter", "ureteral transitional cell carcinoma", "Ureteral Transitional Cell Carcinoma", "Transitional cell carcinoma of ureter", "transitional cell carcinoma of ureter", "Transitional Cell Carcinoma of Ureter", "urothelial cell carcinoma of the ureter", "Urothelial Cell Carcinoma of the Ureter", "Transitional Cell Carcinoma of the Ureter", "transitional cell carcinoma of the ureter", "Transitional cell carcinoma of ureter (disorder)", "transitional cell carcinoma of ureter (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ureter transitional cell carcinoma", "shortest_name_length": 24}
{"curie": "MONDO:0018226", "names": ["XMESID", "Ohtahara Syndrome", "X-Linked West Syndrome", "West Syndrome, X-Linked", "WEST SYNDROME, X-LINKED", "X-linked infantile spasms", "OHTAHARA SYNDROME, X-LINKED", "X-linked infantile spasm syndrome", "Early Infantile Epileptic Encephalopathy", "Developmental and Epileptic Encephalopathy", "infantile epileptic-dyskinetic encephalopathy", "Infantile Epileptic-Dyskinetic Encephalopathy", "Infantile epileptic dyskinetic encephalopathy", "Infantile epileptic-dyskinetic encephalopathy", "INFANTILE EPILEPTIC-DYSKINETIC ENCEPHALOPATHY", "Infantile epileptic dyskinetic encephalopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile epileptic-dyskinetic encephalopathy", "shortest_name_length": 6}
{"curie": "MONDO:0002602", "names": ["中枢神経系疾患", "Choroby OUN", "CNS Disease", "cns disease", "cns disorder", "cns diseases", "CNS disorder", "CNS Diseases", "cns disorders", "CNS DISORDER (NOS)", "cerebrospinal; disorder", "central nervous disease", "encephalomyeloneuropathy", "Encephalomyeloneuropathy", "Keskushermoston sairaudet", "Ziekte, centraalzenuwstelsel-", "Encephalomyeloneuropathy, NOS", "central disease nervous system", "disease central nervous system", "Central nervous system disease", "Central Nervous System Disease", "Zentralnervensystemkrankheiten", "central nervous system disease", "central disorder nervous system", "central diseases nervous system", "central disease nervous systems", "central nervous system disorder", "Central Nervous System Disorder", "DISORDER CENTRAL NERVOUS SYSTEM", "central nervous system diseases", "CENTRAL NERVOUS SYSTEM DISORDER", "Central Nervous System Diseases", "Disorder central nervous system", "Central nervous system disorder", "Central Nervous System Disorders", "central nervous system disorders", "Sykdommer i sentralnervesystemet", "central disorders nervous system", "Centrala nervsystemets sjukdomar", "NERVOUS SYSTEM DISORDER, CENTRAL", "Nervous system disorder, central", "Central nervous system--Diseases", "nervous system; disorder, central", "disease of central nervous system", "SREDIŠNJI ŽIVČANI SUSTAV, BOLESTI", "Doenças do Sistema Nervoso Central", "disorder of central nervous system", "Disorder of Central Nervous System", "Maladie du système nerveux central", "disorders of central nervous system", "Central nervous system disorder NOS", "НЕРВНОЙ СИСТЕМЫ ЦЕНТРАЛЬНОЙ БОЛЕЗНИ", "Central nervous system (CNS) disease", "disease (or disorder); cerebrospinal", "Morphological abnormality of the CNS", "nemoci centrálního nervového systému", "Malattie del sistema nervoso centrale", "disease of the central nervous system", "Disorder of the central nervous system", "Disorder of central nervous system NOS", "Enfermedades del Sistema Nervioso Central", "Abnormality of the central nervous system", "Disease of the central nervous system, NOS", "central nervous system disease or disorder", "disease or disorder of central nervous system", "disease (or disorder); nervous system, central", "Disorder of central nervous system, unspecified", "disorders of central nervous system (diagnosis)", "Morphological central nervous system abnormality", "Disorder of the central nervous system (disorder)", "Morphological abnormality of the central nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system disorder", "shortest_name_length": 7}
{"curie": "MONDO:0000252", "names": ["Inflammatory diarrhea", "diarrhea inflammatory", "inflammatory diarrhea", "Inflammatory diarrhoea", "diarrhea; inflammatory", "inflammatory; diarrhea", "Inflammatory diarrhea (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory diarrhea", "shortest_name_length": 21}
{"curie": "MONDO:0006255", "names": ["INTS", "Intimal Sarcoma", "intimal sarcoma", "Intimal sarcoma", "Intimal sarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intimal sarcoma", "shortest_name_length": 4}
{"curie": "UMLS:C0275522", "names": ["Inapparent Infection", "subclinical infection", "Inapparent Infections", "Infection, Inapparent", "Subclinical Infection", "Subclinical infection", "infection subclinical", "Subclinical Infections", "Infection, Subclinical", "Asymptomatic Infection", "Infection, subclinical", "Asymptomatic Infections", "Infection, Asymptomatic", "Subclinical infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Asymptomatic Infections", "shortest_name_length": 20}
{"curie": "MONDO:0013139", "names": ["SCN2", "SCN 2-Autosomal Dominant", "severe congenital neutropenia 2", "Severe Congenital Neutropenia-2", "Neutropenia, Severe Congenital, Autosomal Dominant 2", "neutropenia, severe congenital 2, autosomal dominant", "NEUTROPENIA, SEVERE CONGENITAL, 2, AUTOSOMAL DOMINANT", "Neutropenia, Severe Congenital, 2, Autosomal Dominant", "neutropenia, severe congenital, 2, autosomal dominant", "GFI1 autosomal dominant severe congenital neutropenia", "Severe Congenital Neutropenia Type 2, Autosomal Dominant", "autosomal dominant severe congenital neutropenia caused by mutation in GFI1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neutropenia, severe congenital, 2, autosomal dominant", "shortest_name_length": 4}
{"curie": "MONDO:0019455", "names": ["APMF", "Acute Panmyelosis", "Acute panmyelosis", "acute panmyelosis", "Panmyelosis (acute)", "myelofibrosis acute", "acute myelofibrosis", "Acute myelofibrosis", "Acute Myelofibrosis", "[M]Acute panmyelosis", "myelofibrosis; acute", "Acute myelosclerosis", "acute myelosclerosis", "acute; myelofibrosis", "Acute Myelosclerosis", "Acute panmyelosis NOS", "Acute myelofibrosis NOS", "acute panmyelosis (diagnosis)", "Acute malignant myelofibrosis", "Acute myelofibrosis (clinical)", "Acute myelofibrosis (disorder)", "Acute myelofibrosis (diagnosis)", "Acute (Malignant) Myelofibrosis", "acute (malignant) myelofibrosis", "Acute (Malignant) Myelosclerosis", "acute (malignant) myelosclerosis", "Myeloproliferative disease, acute", "Acute panmyelosis with myelofibrosis", "acute panmyelosis with myelofibrosis", "Acute Panmyelosis with Myelofibrosis", "Acute myelodysplasia with myelofibrosis", "acute myelodysplasia with myelofibrosis", "acute panmyelosis with myelofibrosis (diagnosis)", "Acute panmyelosis with myelofibrosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute panmyelosis with myelofibrosis", "shortest_name_length": 4}
{"curie": "UMLS:C4521752", "names": ["Stage I Gastric (Stomach) Cancer", "Clinical Stage I Gastric Cancer AJCC v8", "Clinical Stage I Gastric Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage I Gastric Cancer AJCC v8", "shortest_name_length": 32}
{"curie": "MONDO:0005134", "names": ["experimental autoimmune encephalomyelitis", "Encephalomyelitis, Autoimmune, Experimental"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "experimental autoimmune encephalomyelitis", "shortest_name_length": 41}
{"curie": "UMLS:C4763795", "names": ["Refractory T-Cell Prolymphocytic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory T-Cell Prolymphocytic Leukemia", "shortest_name_length": 41}
{"curie": "UMLS:C1879899", "names": ["Breast Tubular Adenoma", "Tubular adenoma of breast", "Tubular adenoma of breast (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tubular adenoma of breast", "shortest_name_length": 22}
{"curie": "MONDO:0030062", "names": ["ARVD14", "ARVC14", "arrhythmogenic right ventricular dysplasia 14", "ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 14", "Arrhythmogenic Right Ventricular Cardiomyopathy 14", "ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 14", "arrhythmogenic right ventricular dysplasia, familial, 14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arrhythmogenic right ventricular dysplasia, familial, 14", "shortest_name_length": 6}
{"curie": "MONDO:0016859", "names": ["blepharophimosis-epicanthus inversus-ptosis due to a CNV", "blepharophimosis types 1 and 2 due to copy number variations", "blepharophimosis-epicanthus inversus-ptosis due to copy number variations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blepharophimosis-epicanthus inversus-ptosis due to copy number variations", "shortest_name_length": 56}
{"curie": "MONDO:0003220", "names": ["gallbladder cancer", "Gallbladder Cancer", "Gallbladder carcinoma", "GALLBLADDER CARCINOMA", "Cancer of Gallbladder", "cancer of gallbladder", "carcinoma gallbladder", "Carcinoma gallbladder", "Gallbladder Carcinoma", "gallbladder carcinoma", "bladder carcinoma gall", "GALL BLADDER CARCINOMA", "gall bladder carcinoma", "GALLBLADDER, CARCINOMA", "Carcinoma;gall bladder", "Carcinoma of Gallbladder", "carcinoma of gallbladder", "CARCINOMA OF GALLBLADDER", "Carcinoma of gallbladder", "Cancer of the Gallbladder", "cancer of the gallbladder", "carcinoma of gall bladder", "carcinoma of the gallbladder", "Carcinoma of the Gallbladder", "carcinoma of the gall bladder", "GALLBLADDER CANCER, CARCINOMA", "Gall bladder carcinoma (adeno)", "Carcinoma of gallbladder (disorder)", "carcinoma of gallbladder (diagnosis)", "Gall bladder carcinoma (adenocarcinoma)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gallbladder carcinoma", "shortest_name_length": 18}
{"curie": "MONDO:0010737", "names": ["SED", "SEDT", "SED Tarda", "X Linked SED", "X-Linked SED", "SED, X-Linked", "X Linked SEDT", "X-Linked SEDT", "SEDT, X-Linked", "SED TARDA, X-LINKED", "Sed tarda, X-linked", "Late Spondyloepiphyseal Dysplasia", "spondyloepiphyseal dysplasia tarda", "spondyloepiphyseal dysplasia, late", "Spondyloepiphyseal Dysplasia, Late", "SPONDYLOEPIPHYSEAL DYSPLASIA, LATE", "SPONDYLOEPIPHYSEAL DYSPLASIA TARDA", "Spondyloepiphyseal dysplasia tarda", "X-linked spondyloepiphyseal dysplasia", "Late Onset Spondyloepiphyseal Dysplasia", "Late-Onset Spondyloepiphyseal Dysplasia", "Spondyloepiphyseal Dysplasia, Late-Onset", "SEDT - Spondyloepiphyseal dysplasia tarda", "X-Linked Spondyloepiphyseal Dysplasia Tarda", "X Linked Spondyloepiphyseal Dysplasia Tarda", "X linked spondyloepiphyseal dysplasia tarda", "spondyloepiphyseal dysplasia tarda X-linked", "X-linked spondyloepiphyseal dysplasia tarda", "Spondyloepiphyseal Dysplasia Tarda, X-Linked", "SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED", "spondyloepiphyseal dysplasia tarda, X-linked", "Spondyloepiphyseal Dysplasia Tarda, X Linked", "Spondyloepiphyseal dysplasia tarda (disorder)", "spondyloepiphyseal dysplasia tarda (diagnosis)", "spondyloepiphyseal dysplasia tarda, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepiphyseal dysplasia tarda, X-linked", "shortest_name_length": 3}
{"curie": "MONDO:0004007", "names": ["DIN", "ductal intraepithelial neoplasia", "Intraductal Proliferative Lesion", "Ductal Intraepithelial Neoplasia", "intraductal proliferative lesion", "Breast Intraductal Proliferative Lesion", "Intraductal proliferative breast lesion", "breast intraductal proliferative lesion", "intraductal proliferative lesion of the breast", "mammary intraepithelial neoplasia, ductal type", "Intraductal Proliferative Lesion of the Breast", "Mammary Intraepithelial Neoplasia, Ductal Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast intraductal proliferative lesion", "shortest_name_length": 3}
{"curie": "MONDO:0800027", "names": ["FPSG", "GPSC", "HDLS", "POLD", "ALSP", "HDLS1", "Neuroaxonal Leukodystrophy", "neuroaxonal leukodystrophy", "subcortical gliosis of Neumann", "SUBCORTICAL GLIOSIS OF NEUMANN", "Subcortical gliosis of Neumann", "Subcortical Gliosis of Neumann", "familial dementia, Neumann type", "Familial dementia, Neumann type", "Dementia, Familial, Neumann Type", "DEMENTIA, FAMILIAL, NEUMANN TYPE", "dementia, familial, Neumann type", "Familial progressive subcortical gliosis", "Pigmentary Orthochromatic Leukodystrophy", "Pigmentary orthochromatic leukodystrophy", "pigmentary orthochromatic leukodystrophy", "familial progressive subcortical gliosis", "gliosis, familial progressive subcortical", "Gliosis, Familial Progressive Subcortical", "GLIOSIS, FAMILIAL PROGRESSIVE SUBCORTICAL", "Hereditary Diffuse Leukoencephalopathy with Spheroids", "Adult-Onset Leukodystrophy with Neuroaxonal Spheroids", "adult-onset leukodystrophy with neuroaxonal spheroids", "hereditary diffuse leukoencephalopathy with spheroids", "Adult-onset leucodystrophy with neuroaxonal spheroids", "Hereditary diffuse leucoencephalopathy with spheroids", "Hereditary diffuse leukoencephalopathy with spheroids", "Adult-onset leukodystrophy with neuroaxonal spheroids", "LEUKOENCEPHALOPATHY, HEREDITARY DIFFUSE, WITH SPHEROIDS", "Leukoencephalopathy, Diffuse Hereditary, With Spheroids", "leukoencephalopathy, diffuse hereditary, with spheroids", "leukoencephalopathy, hereditary diffuse, with spheroids", "leukoencephalopathy, diffuse hereditary, with spheroids 1", "LEUKOENCEPHALOPATHY, HEREDITARY DIFFUSE, WITH SPHEROIDS 1", "HDLS - hereditary diffuse leukoencephalopathy with spheroids", "hereditary diffuse leukoencephalopathy with axonal spheroids", "Hereditary diffuse leucoencephalopathy with axonal spheroids", "Hereditary diffuse leukoencephalopathy with axonal spheroids", "HDLS - hereditary diffuse leucoencephalopathy with spheroids", "Hereditary Diffuse Leukoencephalopathy with Axonal Spheroids", "Hereditary diffuse leukoencephalopathy with spheroids (disorder)", "Autosomal Dominant Leukoencephalopathy with Neuroaxonal Spheroids", "Autosomal dominant leukoencephalopathy with neuroaxonal spheroids", "autosomal dominant leukoencephalopathy with neuroaxonal spheroids", "leukoencephalopathy with neuroaxonal spheroids, autosomal dominant", "Leukoencephalopathy with Neuroaxonal Spheroids, Autosomal Dominant", "LEUKOENCEPHALOPATHY WITH NEUROAXONAL SPHEROIDS, AUTOSOMAL DOMINANT", "Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia", "Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia", "adult-onset leukoencephalopathy with axonal spheroids and pigmented glia", "leukoencephalopathy, adult-onset, with axonal spheroids and pigmented glia", "LEUKOENCEPHALOPATHY, ADULT-ONSET, WITH AXONAL SPHEROIDS AND PIGMENTED GLIA", "Hereditary diffuse leukoencephalopathy with axonal spheroids and pigmented glia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukoencephalopathy, diffuse hereditary, with spheroids 1", "shortest_name_length": 4}
{"curie": "UMLS:C4726540", "names": ["Myeloid Neoplasms with Germline Predisposition without a Preexisting Disorder or Organ Dysfunction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myeloid Neoplasms with Germline Predisposition without a Preexisting Disorder or Organ Dysfunction", "shortest_name_length": 98}
{"curie": "UMLS:C4684889", "names": ["Recurrent Alveolar Rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Alveolar Rhabdomyosarcoma", "shortest_name_length": 35}
{"curie": "UMLS:C3272655", "names": ["Urethritis Cystica and Glandularis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urethritis Cystica and Glandularis", "shortest_name_length": 34}
{"curie": "UMLS:C1710413", "names": ["Thyroid Gland Lipoadenoma", "Thyroid Gland Adenolipoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Lipoadenoma", "shortest_name_length": 25}
{"curie": "UMLS:C1514950", "names": ["Stage I High Grade Burkitt-Like Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I High Grade Burkitt-Like Lymphoma", "shortest_name_length": 40}
{"curie": "MONDO:0005271", "names": ["HYSN", "ALLERGY", "Allergy", "allergy", "Allergy.", "allergies", "Allergies", "Sensitivity", "Allergy NOS", "Allergy, NOS", "Allergic state", "Hypersensitive", "Allergy disorder", "Hypersensitivity", "HYPERSENSITIVITY", "allergic disease", "hypersensitivity", "allergic reaction", "Allergic disorder", "Allergic reaction", "Allergic Reaction", "allergic response", "allergy disorders", "ALLERGIC REACTION", "allergic disorder", "Allergic reactions", "Allergic Reactions", "Reaction, Allergic", "Allergic Disorders", "Hypersensitivities", "Allergic disorders", "allergic disorders", "reaction; allergic", "allergic reactions", "hypersensitivities", "allergic; reaction", "Allergic state, NOS", "Reactions, Allergic", "Hypersensitivity NOS", "Allergic disposition", "Allergy, unspecified", "Allergic reaction NOS", "Allergic reaction, NOS", "ALLERGIC REACTION (NOS)", "Reaction allergic (NOS)", "REACTION ALLERGIC (NOS)", "hypersensitivity symptom", "Hypersensitivity symptom", "ALLERGIC/HYPERSENSITIVITY", "hypersensitivity symptoms", "Hypersensitivity reaction", "hypersensitivity reaction", "reaction; hypersensitivity", "hypersensitivity; reaction", "hypersensitivity reactions", "Hypersensitivity reactions", "Allergic reaction (disorder)", "allergic disease or disorder", "allergic reaction (diagnosis)", "Allergy/allergic reaction nos", "Allergy/allergic reaction NOS", "Hypersensitivity reaction, NOS", "Allergic disposition (finding)", "Allergic reaction to substance", "Hypersensitivity reaction (NOS)", "HYPERSENSITIVITY REACTION (NOS)", "Reaction hypersensitivity (NOS)", "type I hypersensitivity disease", "REACTION HYPERSENSITIVITY (NOS)", "allergic hypersensitivity disease", "disorder of type I hypersensitivity", "allergic form of disease or disorder", "Hypersensitivity reaction (disorder)", "hypersensitivity reaction (diagnosis)", "Allergic reaction caused by substance", "allergic form of immune system disease", "hypersensitivity reaction type I disease", "Allergic reaction caused by substance (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "allergic disease", "shortest_name_length": 4}
{"curie": "MONDO:0016019", "names": ["RE", "CFE", "Rasmussen Syndrome", "Rasmussen syndrome", "rasmussen syndrome", "Rasmussen's Syndrome", "rasmussen's syndrome", "Rasmussen encephalitis", "rasmussen encephalitis", "Rasmussen Encephalitis", "Encephalitis, Rasmussen", "encephalitis rasmussens", "chronic focal encephalitis", "Chronic Focal Encephalitis", "Chronic focal encephalitis", "Rasmussen syndrome (disorder)", "Rasmussen syndrome (diagnosis)", "Rasmussen Subacute Encephalitis", "Rasmussen subacute encephalitis", "Subacute focal encephalitis of Rasmussen"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rasmussen subacute encephalitis", "shortest_name_length": 2}
{"curie": "MONDO:0009370", "names": ["L2HGA", "L-2-HGA", "L-2-hydroxyglutaric acidemia", "L-2-hydroxyglutaric aciduria", "L-2-HYDROXYGLUTARIC ACIDEMIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "L-2-hydroxyglutaric aciduria", "shortest_name_length": 5}
{"curie": "MONDO:0019755", "names": ["malformation syndrome", "Multiple congenital anomalies", "embryonic morphogenesis disease", "congenital malformation syndrome", "Congenital malformation syndrome", "Congenital Malformation Syndrome", "congenital malformation syndromes", "Multiple congenital malformations", "disorder of embryonic morphogenesis", "developmental defect during embryogenesis", "Congenital malformation syndrome (disorder)", "congenital malformation syndromes (diagnosis)", "rare developmental defect during embryogenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental defect during embryogenesis", "shortest_name_length": 21}
{"curie": "MONDO:0013239", "names": ["SPG41", "hereditary spastic paraplegia 41", "hereditary spastic paraplegia type 41", "autosomal dominant spastic paraplegia 41", "spastic paraplegia 41, autosomal dominant", "SPASTIC PARAPLEGIA 41, AUTOSOMAL DOMINANT", "Autosomal dominant spastic paraplegia type 41", "autosomal dominant spastic paraplegia type 41", "familial spastic paraplegia autosomal dominant type 41", "Autosomal dominant spastic paraplegia type 41 (disorder)", "Autosomal dominant spastic paraplegia type 41 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 41", "shortest_name_length": 5}
{"curie": "MONDO:0013236", "names": ["PNCA3", "Pnca3", "PALB2 familial pancreatic carcinoma", "susceptibility to pancreatic cancer 3", "pancreatic cancer, susceptibility to, 3", "PANCREATIC CANCER, SUSCEPTIBILITY TO, 3", "pancreatic cancer, susceptibility to, type 3", "familial pancreatic carcinoma caused by mutation in PALB2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic cancer, susceptibility to, 3", "shortest_name_length": 5}
{"curie": "MONDO:0014011", "names": ["ARCI10", "autosomal recessive congenital ichthyosis 10", "ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 10", "ichthyosis, congenital, autosomal recessive 10", "autosomal recessive congenital ichthyosis type 10", "ichthyosis, congenital, autosomal recessive type 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive congenital ichthyosis 10", "shortest_name_length": 6}
{"curie": "MONDO:0000045", "names": ["hypothyroidism, congenital, nongoitrous"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypothyroidism, congenital, nongoitrous", "shortest_name_length": 39}
{"curie": "MONDO:0054560", "names": ["ANXD1", "anauxetic dysplasia", "ANAUXETIC DYSPLASIA 1", "anauxetic dysplasia 1", "spondylometaepiphyseal dysplasia, Menger type", "spondyloepimetaphyseal dysplasia, anauxetic type", "spondylometaepiphyseal dysplasia, anauxetic type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anauxetic dysplasia 1", "shortest_name_length": 5}
{"curie": "UMLS:C4287594", "names": ["High Grade ESS", "YWHAE-FAM22 ESS", "Uterine Corpus High Grade ESS", "YWHAE-FAM22 Endometrial Stromal Sarcoma", "Uterine Corpus High Grade Endometrial Stromal Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Corpus High Grade Endometrial Stromal Sarcoma", "shortest_name_length": 14}
{"curie": "UMLS:C4324332", "names": ["Allergic reaction to excipient"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Allergic reaction to excipient", "shortest_name_length": 30}
{"curie": "MONDO:0012635", "names": ["CDG2H", "CDGIIH", "CDGIIh", "CDG-IIh", "CDG IIh", "CDGIIdh", "CDG IIIH", "COG8-CDG", "COG8-CDG (CDG-IIh)", "CDG syndrome type IIh", "COG8-congenital disorder of glycosylation", "COG8 congenital disorder of glycosylation", "congenital disorder of glycosylation type 2h", "Congenital disorder of glycosylation type 2h", "congenital disorder of glycosylation type IIh", "Congenital disorder of glycosylation type IIh", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIh", "congenital disorder of glycosylation, type IIh", "Congenital Disorder Of Glycosylation, Type IIH", "carbohydrate deficient glycoprotein syndrome type IIh", "Carbohydrate deficient glycoprotein syndrome type IIh", "Component of oligomeric golgi complex 8 congenital disorder of glycosylation", "COG8 (component of oligomeric golgi complex 8) congenital disorder of glycosylation", "Component of oligomeric golgi complex 8 congenital disorder of glycosylation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "COG8-congenital disorder of glycosylation", "shortest_name_length": 5}
{"curie": "MONDO:0001811", "names": ["Tetanic Cataract", "tetanic cataract", "Tetanic cataract", "Hypocalcemic cataract", "Hypocalcaemic cataract", "hypocalcaemic cataract", "Tetanic cataract (disorder)", "tetanic cataract (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tetanic cataract", "shortest_name_length": 16}
{"curie": "MONDO:0009310", "names": ["CDG2", "CGD2", "NCF2 DEFICIENCY", "deficiency of NCF2", "Ncf2, deficiency of", "p67-PHOX DEFICIENCY", "deficiency of p67-PHOX", "P67-PHOX, deficiency of", "P67-Phox, Deficiency of", "NCF2 chronic granulomatous disease", "NEUTROPHIL CYTOSOL FACTOR 2 DEFICIENCY", "Neutrophil Cytosol Factor 2, Deficiency of", "neutrophil cytosol Factor 2, deficiency of", "autosomal recessive chronic granulomatous disease 2", "chronic granulomatous disease 2, autosomal recessive", "GRANULOMATOUS DISEASE, CHRONIC, DUE TO NCF2 DEFICIENCY", "CGD, autosomal recessive cytochrome B-positive, type 2", "granulomatous disease, chronic, due to Ncf2 deficiency", "Granulomatous Disease, Chronic, due to NCF2 Deficiency", "GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, 2", "CGD, AUTOSOMAL RECESSIVE CYTOCHROME b-POSITIVE, TYPE II", "CGD, Autosomal Recessive Cytochrome B-Positive, Type II", "chronic granulomatous disease caused by mutation in NCF2", "chronic granulomatous disease due to deficiency of NCF-2", "autosomal recessive chronic granulomatous disease cytochrome b-positive type II", "granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2", "granulomatous disease, chronic, autosomal recessive, cytochrome b-POSITIVE, type II", "Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II", "GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2", "shortest_name_length": 4}
{"curie": "UMLS:C5237054", "names": ["Recurrent Endometrial Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Endometrial Squamous Cell Carcinoma", "shortest_name_length": 45}
{"curie": "UMLS:C0948599", "names": ["Candida pneumonia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Candida pneumonia", "shortest_name_length": 17}
{"curie": "UMLS:C4330470", "names": ["Iatrogenic Hypoparathyroidism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Iatrogenic Hypoparathyroidism", "shortest_name_length": 29}
{"curie": "MONDO:0017981", "names": ["syngnathia cleft palate", "syngnathia-cleft palate syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syngnathia-cleft palate syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0014622", "names": ["FNEPPK", "FNEPPK2", "focal nonepidermolytic palmoplantar keratoderma", "focal nonepidermolytic palmoplantar keratoderma 2", "PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL 2", "palmoplantar keratoderma, nonepidermolytic, focal 2", "palmoplantar keratoderma, nonepidermolytic, focal type 2", "isolated focal non-epidermolytic palmoplantar keratoderma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated focal non-epidermolytic palmoplantar keratoderma", "shortest_name_length": 6}
{"curie": "UMLS:C4721431", "names": ["Stage IV Oropharyngeal SCC", "Stage IV SCC of Oropharynx", "Stage IV SCC of the Oropharynx", "Stage IV Oropharynx Epidermoid Carcinoma", "Stage IV Epidermoid Carcinoma of Oropharynx", "Stage IV Oropharyngeal Epidermoid Carcinoma", "Stage IV Oropharynx Squamous Cell Carcinoma", "Stage IV Oropharyngeal Squamous Cell Carcinoma", "Stage IV Squamous Cell Carcinoma of Oropharynx", "Stage IV Epidermoid Carcinoma of the Oropharynx", "Stage IV Squamous Cell Carcinoma of the Oropharynx", "Stage IV Oropharyngeal Throat Squamous Cell Cancer", "Stage IV Oropharyngeal Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Oropharyngeal Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 26}
{"curie": "MONDO:0012801", "names": ["AUTS15", "autism susceptibility 15", "susceptibility to autism 15", "AUTISM, SUSCEPTIBILITY TO, 15", "autism, susceptibility to, 15", "autism, susceptibility to, type 15"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autism, susceptibility to, 15", "shortest_name_length": 6}
{"curie": "MONDO:0030514", "names": ["HLD23", "hypomyelinating leukodystrophy 23", "LEUKODYSTROPHY, HYPOMYELINATING, 23, WITH ATAXIA, DEAFNESS, LIVER DYSFUNCTION, AND DILATED CARDIOMYOPATHY", "leukodystrophy, hypomyelinating, 23, with ataxia, deafness, liver dysfunction, and dilated cardiomyopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukodystrophy, hypomyelinating, 23, with ataxia, deafness, liver dysfunction, and dilated cardiomyopathy", "shortest_name_length": 5}
{"curie": "UMLS:C0542118", "names": ["Nevus spider congenital", "Congenital Spider Nevus", "NEVUS SPIDER CONGENITAL", "Congenital Nevus Araneus", "Naevus spider congenital"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nevus spider congenital", "shortest_name_length": 23}
{"curie": "MONDO:0043230", "names": ["ciguatera", "Ciguatera", "poisoning fish", "fish poisoning", "ciguatera poison", "Ciguatera Poisoning", "CIGUATERA POISONING", "Poisoning;ciguatera", "ciguatera poisoning", "Ciguatera Poisonings", "Poisoning, Ciguatera", "poisoning, ciguatera", "ciguatera Poisonings", "Poisonings, ciguatera", "Poisonings, Ciguatera", "ciguatera fish poisoning", "Ciguatera Fish Poisoning", "Ciguatera fish poisoning", "ciguatera fish; poisoning", "Ciguatera Fish Poisonings", "poisoning, ciguatera fish", "ciguatera fish Poisonings", "poisoning; ciguatera fish", "Poisoning, Ciguatera Fish", "Poisonings, ciguatera fish", "Poisonings, Ciguatera Fish", "ciguatera fish; ichthyotoxism", "ichthyotoxism; ciguatera fish", "Ciguatoxin causing toxic effect", "ciguatoxin causing toxic effect", "ciguatera poisoning (diagnosis)", "Toxic effect of ciguatera fish poisoning", "toxic effect of ciguatera fish poisoning", "Ciguatoxin causing toxic effect (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ciguatera fish poisoning", "shortest_name_length": 9}
{"curie": "MONDO:0011663", "names": ["PLSJ", "JPLS", "Juvenile PLS", "juvenile PLS", "PLS juvenile", "Pls, juvenile", "PLS, JUVENILE", "Juvenile primary lateral sclerosis", "Juvenile Primary Lateral Sclerosis", "Primary lateral sclerosis juvenile", "juvenile primary lateral sclerosis", "primary lateral sclerosis, juvenile", "Primary Lateral Sclerosis, Juvenile", "PRIMARY LATERAL SCLEROSIS, JUVENILE", "Juvenile primary lateral sclerosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile primary lateral sclerosis", "shortest_name_length": 4}
{"curie": "UMLS:C0151490", "names": ["CNS congenital anomaly", "CNS CONGENITAL ANOMALY", "Congenital CNS anomaly NOS", "Congenital central nervous system anomaly", "Central nervous system congenital anomaly", "Congenital anomaly of central nervous system", "Congenital central nervous system anomaly NOS", "Congenital Central Nervous System Malformations", "congenital malformations nervous system central", "ANOMALY CONGENITAL CENTRAL NERVOUS SYSTEM (NOS)", "Congenital malformation of central nervous system", "congenital malformation of central nervous system", "Malformation of central nervous system, congenital", "Congenital anomaly of central nervous system (disorder)", "congenital malformation of central nervous system (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital anomaly of central nervous system", "shortest_name_length": 22}
{"curie": "MONDO:0020725", "names": ["acd", "acds", "Secondary anemia", "chronic anemia disease", "chronic disease anemia", "anemia chronic disease", "ANEMIA CHRONIC DISEASE", "anemia chronic diseases", "anemias chronic disease", "anaemia chronic disease", "Anaemia;chronic disease", "anaemia chronic diseases", "anemia of chronic illness", "Anemia Of Chronic Disease", "anemia of chronic disease", "Anemia of Chronic Illness", "Anemia in chronic illness", "Anemia of chronic disease", "ANEMIA OF CHRONIC DISEASE", "Anemia of Chronic Disease", "anaemia of chronic disease", "Anemia of systemic disease", "anemia of systemic disease", "anemia of chronic disorder", "Anemia of chronic disorder", "Anaemia of chronic disease", "Anaemia of chronic disorder", "Anemia with chronic illness", "Anaemia of systemic disease", "Anemia due to Chronic Disorder", "anemia due to chronic disorder", "anemia due to Chronic Disorder", "Anemia of chronic inflammation", "anemia of chronic inflammation", "Anemia of Chronic Inflammation", "Anemia of chronic disorder, NOS", "Anaemia of chronic inflammation", "Anaemia of chronic disorder, NOS", "Anemias due to chronic disorders", "Anaemias due to chronic disorders", "anemia of chronic disease (diagnosis)", "Anemia of chronic disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anemia due to chronic disorder", "shortest_name_length": 3}
{"curie": "MONDO:0005530", "names": ["Narcotism", "narcotism", "Opiate Addiction", "Opioid addiction", "opiate addiction", "addiction opiate", "Opioid Addiction", "opiate dependence", "Addiction, Opioid", "opioid dependence", "Addiction, Opiate", "Opioid Dependence", "OPIOID DEPENDENCE", "Opioid Addictions", "Opiate Dependence", "Opioid dependence", "Dependence, Opiate", "dependence; opiate", "dependence opiates", "Dependence, Opioid", "Opioid Dependences", "dependence narcotic", "narcotic dependence", "dependence; opioids", "opioids; dependence", "Dependence on opiates", "dependence on opiates", "opioid type dependence", "Opioid type dependence", "Opioid-Related Disorder", "Opioid Related Disorders", "Opioid-related disorders", "Opioid related disorders", "opioid-related disorders", "Opioid-Related Disorders", "Opioid type drug dependence", "Opioid dependence (disorder)", "opioid dependence (diagnosis)", "Opioid type dependence, unspecified", "opioid-related disorders (diagnosis)", "Opioid type dependence, unspecified use"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "opiate dependence", "shortest_name_length": 9}
{"curie": "UMLS:C0278573", "names": ["Mycosis fungoides stage IV", "Stage IV Mycosis Fungoides", "Mycosis Fungoides Stage IV", "Stage IV Mycosis Fungoides AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mycosis fungoides stage IV", "shortest_name_length": 26}
{"curie": "UMLS:C4525470", "names": ["Tumor Stage (Pathological)", "Pancreatic Cancer by AJCC v8 Stage", "Exocrine Pancreatic Cancer by AJCC v8 Stage", "Exocrine Pancreatic Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Cancer by AJCC v8 Stage", "shortest_name_length": 26}
{"curie": "MONDO:0008518", "names": ["WL syndrome", "synostosis multiplex", "Symphalangism syndrome", "polysynostoses syndrome", "Facio-audio-symphalangism", "Calcaneonavicular coalition", "calcaneonavicular coalition", "CALCANEONAVICULAR COALITION", "multiple synostoses syndrome", "Multiple synostoses syndrome", "Multiple synostosis syndrome", "multiple synostosis syndrome", "Symphalangism-brachydactyly syndrome", "SYNOSTOSES, TARSAL, CARPAL AND DIGITAL", "synostoses, tarsal, carpal and digital", "synostoses, tarsal, carpal, and digital", "calcaneonavicular coalition (diagnosis)", "SYNOSTOSES, TARSAL, CARPAL, AND DIGITAL", "Synostoses, tarsal, carpal, and digital", "Multiple synostosis syndrome (disorder)", "Deafness-Hermann type symphalangism syndrome", "Hearing loss-Hermann type symphalangism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "calcaneonavicular coalition", "shortest_name_length": 11}
{"curie": "MONDO:0004719", "names": ["hard palate", "hard palate cancer", "cancer of hard palate", "Malignant Hard Palate Tumor", "malignant hard palate tumor", "malignant tumor of hard palate", "Malignant tumor of hard palate", "Malignant Tumor of Hard Palate", "Malignant Hard Palate Neoplasm", "malignant hard palate neoplasm", "malignant tumour of hard palate", "Malignant tumour of hard palate", "malignant neoplasm of hard palate", "Malignant Neoplasm of Hard Palate", "Malignant neoplasm of hard palate", "malignant tumor of the hard palate", "Malignant Tumor of the Hard Palate", "Malignant Neoplasm of the Hard Palate", "malignant neoplasm of the hard palate", "Malignant tumor of hard palate (disorder)", "malignant neoplasm of hard palate (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hard palate cancer", "shortest_name_length": 11}
{"curie": "UMLS:C5555178", "names": ["Refractory Fallopian Tube Serous Adenocarcinoma", "Refractory High Grade Fallopian Tube Serous Adenocarcinoma", "Refractory Fallopian Tube High Grade Serous Adenocarcinoma", "Refractory Fallopian Tube High-Grade Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Fallopian Tube High Grade Serous Adenocarcinoma", "shortest_name_length": 47}
{"curie": "MONDO:0010450", "names": ["MRX89", "XLID89", "X-linked mental retardation 89", "MENTAL RETARDATION, X-LINKED 89", "mental retardation, X-linked 89", "Mental Retardation, X-Linked 89", "intellectual disability, X-linked 89", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 89", "non-syndromic X-linked intellectual disability 89", "mental retardation, X-linked 89, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 89", "shortest_name_length": 5}
{"curie": "MONDO:0010436", "names": ["Gdi1 Duplication Syndrome", "CHROMOSOME Xq28 DUPLICATION SYNDROME", "Chromosome Xq28 Duplication Syndrome", "chromosome Xq28 duplication syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome Xq28 duplication syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0009423", "names": ["Gullner syndrome", "GULLNER SYNDROME", "Gullner Syndrome", "Gullner's syndrome", "Familial hypokalemia", "Hypokalemia, Familial", "Familial hypokalaemia", "HYPOKALEMIA, FAMILIAL", "hypokalemia, familial", "Familial hypokalemic alkalosis, Gullner type", "Familial hypokalaemic alkalosis, Gullner type", "Familial hypokalemic alkalosis, Gullner type (disorder)", "Hypokalemic Alkalosis, Familial, with Specific Renal Tubulopathy", "hypokalemic alkalosis, familial, with specific renal tubulopathy", "HYPOKALEMIC ALKALOSIS, FAMILIAL, WITH SPECIFIC RENAL TUBULOPATHY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypokalemic alkalosis, familial, with specific renal tubulopathy", "shortest_name_length": 16}
{"curie": "MONDO:0017993", "names": ["CSVT", "cerebral sinovenous thrombosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral sinovenous thrombosis", "shortest_name_length": 4}
{"curie": "UMLS:C1511256", "names": ["Borderline Fallopian Tube Tumor", "Borderline Fallopian Tube Neoplasm", "Fallopian Tube Neoplasm of Low Malignant Potential"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Fallopian Tube Neoplasm", "shortest_name_length": 31}
{"curie": "MONDO:0010304", "names": ["Grdx1", "GRDX1", "GRDX2", "Graves disease, susceptibility to, X-linked", "Graves disease, susceptibility to, X-linked 1", "GRAVES DISEASE, SUSCEPTIBILITY TO, X-LINKED 1", "GRAVES DISEASE, SUSCEPTIBILITY TO, X-LINKED 2", "Graves disease, susceptibility to, X-linked 2", "Graves disease, susceptibility to, X-linked type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Graves disease, susceptibility to, X-linked 1", "shortest_name_length": 5}
{"curie": "MONDO:0100401", "names": ["AML, del(5q31-q32)", "AML, del(5)(q31q32)", "AML, del(5)(q31-q32)", "AML, 5q31-32 Deletion", "acute myeloid leukemia, del(5q31-q32)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, del(5q31-q32)", "shortest_name_length": 18}
{"curie": "MONDO:0020294", "names": ["atrial defect and interatrial communication", "atrial defect and interauricular communication", "rare atrial defect and interatrial communication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial defect and interatrial communication", "shortest_name_length": 43}
{"curie": "MONDO:0017251", "names": ["CPAM type 3", "CCAM type 3", "congenital cystic disease of the lung type 3", "congenital pulmonary airway malformation type 3", "congenital cystic adenomatous malformation of the lung type 3", "congenital cystic adenomatoid malformation of the lung type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital pulmonary airway malformation type 3", "shortest_name_length": 11}
{"curie": "UMLS:C5669691", "names": ["Locally Recurrent Chordoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Recurrent Chordoma", "shortest_name_length": 26}
{"curie": "MONDO:0005817", "names": ["Klver-Bucy syndrome", "Kluver Bucy syndrome", "kluver bucy syndrome", "KLüver-Bucy syndrome", "Kluver-Bucy Syndrome", "Kluver-Bucy syndrome", "Kluver Bucy Syndrome", "Klüver-Bucy syndrome", "kluver-bucy syndrome", "KLuever-Bucy syndrome", "Syndrome, Kluver-Bucy", "syndrome, Kluver-Bucy", "bilateral temporal lobe disorder", "temporal lobectomy behavior syndrome", "Temporal Lobectomy Behavior Syndrome", "Temporal lobectomy behavior syndrome", "Temporal lobectomy behaviour syndrome", "post-traumatic Kluver Bucy syndrome (type)", "post-encephalitic Kluver Bucy syndrome (type)", "Temporal lobectomy behavior syndrome (disorder)", "memory loss, extreme sexual behavior, placidity, and visual distractibility"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kluver-Bucy syndrome", "shortest_name_length": 19}
{"curie": "MONDO:0002300", "names": ["dermis tumor", "dermal tumor", "Dermal Tumor", "dermis tumour", "Tumor of dermis", "dermal neoplasm", "dermis neoplasm", "Tumor of Dermis", "Dermal Neoplasm", "tumor of dermis", "Tumour of dermis", "tumour of dermis", "neoplasm of dermis", "neoplasm of Dermis", "Neoplasm of Dermis", "tumor of the dermis", "Tumor of the Dermis", "Neoplasm of the Dermis", "neoplasm of the dermis", "Tumor of the dermis NOS", "dermis neoplasm (disease)", "Tumor of dermis (navigational concept)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermis tumor", "shortest_name_length": 12}
{"curie": "UMLS:C4727167", "names": ["Metastatic Unresectable Gastric Adenocarcinoma", "Metastatic Unresectable Gastric (Stomach) Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Unresectable Gastric Adenocarcinoma", "shortest_name_length": 46}
{"curie": "MONDO:0016122", "names": ["Episodic paralysis", "periodic paralysis", "Periodic paralysis", "periodic paralysis syndrome", "periodic paralysis (disease)", "Periodic paralysis (finding)", "periodic paralysis (finding)", "periodic paralysis syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "periodic paralysis", "shortest_name_length": 18}
{"curie": "UMLS:C0887799", "names": ["Posterior Choroidal Artery Infarction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Posterior Choroidal Artery Infarction", "shortest_name_length": 37}
{"curie": "MONDO:0012157", "names": ["FIM1", "CMS1D", "CMS4C", "Cms Id", "CMS Id", "FIM1, FORMERLY", "CMS1D, FORMERLY", "CMS Id, FORMERLY", "Cms Id, formerly", "familial infantile myasthenia 1", "myasthenia, familial infantile, 1", "congenital myasthenic syndrome 4C", "Congenital Myasthenic Syndrome-4C", "congenital myasthenic syndrome type Id", "congenital myasthenic syndrome type 4C", "myasthenic syndrome, congenital, type Id", "Myasthenic syndrome, congenital, type Id", "MYASTHENIC SYNDROME, CONGENITAL, TYPE Id", "myasthenia, familial infantile, 1, formerly", "MYASTHENIA, FAMILIAL INFANTILE, 1, FORMERLY", "congenital myasthenic syndrome associated with acetylcholine receptor deficiency", "myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency", "Myasthenic Syndrome, Congenital, Associated With Acetylcholine Receptor Deficiency", "MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY", "congenital myasthenic syndrome 4C associated with acetylcholine receptor deficiency", "myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency", "MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY", "Myasthenic Syndrome, Congenital, 4C, Associated with Acetylcholine Receptor Deficiency", "Myasthenic Syndrome, Congenital, Postsynaptic, Associated With Acetylcholine Receptor Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myasthenic syndrome 4C", "shortest_name_length": 4}
{"curie": "UMLS:C1302752", "names": ["Graze", "Abraded", "abraded", "Abrading", "ABRASION", "abrasion", "abrading", "Abrasion", "ABRASIONS", "Abrasions", "Abrasion NOS", "ABRASION NOS", "Abrasion, NOS", "Abrasion (disorder)", "Superficial abrasion", "Abrasion, unspecified", "abrasion (physical finding)", "abrasion (see also by location)", "Abrasion (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abrasion", "shortest_name_length": 5}
{"curie": "MONDO:0002651", "names": ["Anal Paget Disease", "anal Paget disease", "anus Paget disease", "anal Paget's disease", "Anal Paget's Disease", "Paget's Disease of Anus", "Paget's disease of anus", "Paget disease of the anus", "Paget; extramammary, anal", "Paget Disease of the Anus", "extramammary; Paget, anal", "Paget's disease of the anus", "Paget's Disease of the Anus", "anus mammary Paget's disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anal Paget disease", "shortest_name_length": 18}
{"curie": "UMLS:C1504532", "names": ["post-transplant diabetes mellitus", "Post transplant diabetes mellitus", "post-transplant diabetes mellitus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post transplant diabetes mellitus", "shortest_name_length": 33}
{"curie": "MONDO:0015491", "names": ["immune complex mediated vasculitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immune complex mediated vasculitis", "shortest_name_length": 34}
{"curie": "MONDO:0007450", "names": ["CDI", "AVP deficiency", "ADH deficiency", "hereditary CDI", "ADH Deficiency", "Vasopressin deficiency", "Vasopressin Deficiency", "vasopressin deficiency", "cranial diabetes insipidus", "Cranial diabetes insipidus", "central diabetes insipidus", "Central Diabetes Insipidus", "Central diabetes insipidus", "Diabetes Insipidus, Central", "pituitary diabetes insipidus", "Pituitary diabetes insipidus", "Pituitary Diabetes Insipidus", "Diabetes Insipidus, Pituitary", "neurogenic diabetes insipidus", "Neurogenic Diabetes Insipidus", "Neurogenic diabetes insipidus", "pituitary; diabetes insipidus", "Diabetes insipidus - pituitary", "Diabetes insipidus, neurogenic", "diabetes; insipidus, pituitary", "Diabetes Insipidus, Neurogenic", "antidiuretic hormone deficiency", "Antidiuretic hormone deficiency", "Antidiuretic Hormone Deficiency", "Vasopressin deficiency syndrome", "Arginine vasopressin deficiency", "Arginine Vasopressin Deficiency", "Diabetes Insipidus Cranial Type", "diabetes insipidus, cranial type", "DIABETES INSIPIDUS, CRANIAL TYPE", "Diabetes Insipidus, Cranial Type", "pituitary gland diabetes insipidus", "Primary central diabetes insipidus", "Diabetes Insipidus Primary Central", "DIABETES INSIPIDUS, PRIMARY CENTRAL", "diabetes insipidus, primary central", "Neurohypophyseal Diabetes Insipidus", "Diabetes Insipidus, Primary Central", "neurohypophyseal diabetes insipidus", "Neurohypophyseal diabetes insipidus", "X-linked central diabetes insipidus", "Diabetes Insipidus, Neurohypophyseal", "diabetes insipidus, neurohypophyseal", "DIABETES INSIPIDUS, NEUROHYPOPHYSEAL", "hereditary central diabetes insipidus", "diabetes insipidus of pituitary gland", "antidiuretic hormone defective syndrome", "Vasopressin Defective Diabetes Insipidus", "Neurohypophyseal diabetes insipidus, NOS", "vasopressin defective diabetes insipidus", "hereditary neurogenic diabetes insipidus", "Diabetes Insipidus, Neurohypophyseal Type", "X-linked neurohypophyseal diabetes insipidus", "Neurohypophyseal diabetes insipidus (disorder)", "DIABETES INSIPIDUS, NEUROHYPOPHYSEAL, X-LINKED", "Neurohypophyseal diabetes insipidus (diagnosis)", "Diabetes insipidus secondary to vasopressin deficiency", "Diabetes Insipidus Secondary To Vasopressin Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurohypophyseal diabetes insipidus", "shortest_name_length": 3}
{"curie": "MONDO:0011920", "names": ["DFNA48", "autosomal dominant deafness 48", "DEAFNESS, AUTOSOMAL DOMINANT 48", "Deafness, Autosomal Dominant 48", "deafness, autosomal dominant 48", "deafness, autosomal dominant type 48", "autosomal dominant nonsyndromic deafness 48", "MYO1A autosomal dominant nonsyndromic deafness", "autosomal dominant nonsyndromic hearing loss 48", "autosomal dominant nonsyndromic deafness type 48", "autosomal dominant nonsyndromic deafness caused by mutation in MYO1A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 48", "shortest_name_length": 6}
{"curie": "UMLS:C0340664", "names": ["Coronary artery perforation", "Coronary Artery Perforation", "Coronary artery perforation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Coronary artery perforation", "shortest_name_length": 27}
{"curie": "UMLS:C5557310", "names": ["DS Stage IA Plasma Cell Myeloma", "Durie/Salmon Stage IA Plasma Cell Myeloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DS Stage IA Plasma Cell Myeloma", "shortest_name_length": 31}
{"curie": "MONDO:0100058", "names": ["HVLI", "BRANCHED-CHAIN AMINOTRANSFERASE DEFICIENCY", "branched-chain aminotransferase deficiency", "hypervalinemia or hyperleucine-isoleucinemia", "HYPERVALINEMIA AND HYPERLEUCINE-ISOLEUCINEMIA", "hypervalinemia and hyperleucine-isoleucinemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypervalinemia and hyperleucine-isoleucinemia", "shortest_name_length": 4}
{"curie": "UMLS:C5239113", "names": ["Recurrent Follicular T-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Follicular T-Cell Lymphoma", "shortest_name_length": 36}
{"curie": "MONDO:0033856", "names": ["LAMA5-related multisystemic syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "LAMA5-related multisystemic syndrome", "shortest_name_length": 36}
{"curie": "UMLS:C3146261", "names": ["Stage II Prostate Cancer", "Stage II Prostate Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Prostate Cancer AJCC v7", "shortest_name_length": 24}
{"curie": "MONDO:0008193", "names": ["Willige-Hunt", "Pallidal atrophy", "Pallidal syndrome", "Neostriatal syndrome", "Paleostriatal syndrome", "Ramsay Hunt's syndrome 3", "Hunt's striatal syndrome (1)", "Hunt's striatal syndrome (2)", "HUNT CORPUS STRIATUM SYNDROME", "PARKINSONISM, JUVENILE, OF HUNT", "Juvenile paralysis agitans of Hunt", "Parkinson Disease, Juvenile, Of Hunt", "paralysis agitans, juvenile, of Hunt", "Paralysis Agitans, Juvenile, Of Hunt", "PARALYSIS AGITANS, JUVENILE, OF HUNT", "PARKINSON DISEASE, JUVENILE, OF HUNT", "Parkinson disease, juvenile, of Hunt", "Juvenile paralysis agitans of Hunt (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paralysis agitans, juvenile, of Hunt", "shortest_name_length": 12}
{"curie": "MONDO:0034147", "names": ["neonatal epileptic encephalopathy due to glutaminase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal epileptic encephalopathy due to glutaminase deficiency", "shortest_name_length": 63}
{"curie": "MONDO:0016525", "names": ["FH", "genetic hyperaldosteronism", "Familial Hyperaldosteronism", "familial hyperaldosteronism", "Familial hyperaldosteronism", "hereditary hyperaldosteronism", "Familial hyperaldosteronism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial hyperaldosteronism", "shortest_name_length": 2}
{"curie": "MONDO:0008762", "names": ["ATS2", "nephropathy and deafness", "Alport syndrome recessive type", "autosomal recessive Alport syndrome", "Autosomal recessive Alport syndrome", "Alport syndrome autosomal recessive", "Alport syndrome, autosomal recessive", "Alport Syndrome, Autosomal Recessive", "Alport syndrome 2, autosomal recessive", "ALPORT SYNDROME 2, AUTOSOMAL RECESSIVE", "Alport syndrome autosomal recessive (disorder)", "Alport syndrome autosomal recessive (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive Alport syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C1335699", "names": ["Recurrent Pediatric Visual Pathway Astrocytoma", "Recurrent Childhood Visual Pathway Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Visual Pathway Astrocytoma", "shortest_name_length": 46}
{"curie": "UMLS:C0563671", "names": ["injury; peritoneum", "peritoneum; injury", "Injury of peritoneum", "injury of peritoneum", "Injury to Peritoneum", "Injury of peritoneum (disorder)", "injury of peritoneum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of peritoneum", "shortest_name_length": 18}
{"curie": "UMLS:C0022822", "names": ["Gibbus", "Kyphosis", "acquired kyphosis", "Acquired kyphosis", "Acquired Kyphosis", "Acquired hunchback", "Kyphosis (acquired)", "Hunchback (acquired)", "Acquired kyphosis (disorder)", "hunchback formed after birth", "acquired kyphosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired kyphosis", "shortest_name_length": 6}
{"curie": "MONDO:0000321", "names": ["Typhoidal tularemia", "typhoidal tularemia", "Typhoidal tularaemia", "tularemia; typhoidal", "typhoidal; tularemia", "Cryptogenic tularemia", "Non-specific tularemia", "Cryptogenic tularaemia", "Non-specific tularaemia", "Typhoidal tularemia (disorder)", "typhoidal tularemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "typhoidal tularemia", "shortest_name_length": 19}
{"curie": "MONDO:0019877", "names": ["Trisomy 2qter", "trisomy 2qter", "distal trisomy 2q", "Distal trisomy 2q", "Distal duplication 2q", "distal duplication 2q", "distal trisomy type 2q", "telomeric duplication 2q", "Telomeric duplication 2q", "Distal trisomy 2q (disorder)", "Distal trisomy 2q (diagnosis)", "anomaly of chromosome pair distal trisomy 2q"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal trisomy 2q", "shortest_name_length": 13}
{"curie": "MONDO:0017844", "names": ["SS", "Sézary", "Sézary disease", "Sezary disease", "Sezary lymphoma", "SEZARY SYNDROME", "Sezary Syndrome", "sezary syndrome", "Sézary syndrome", "Sézary Syndrome", "Sezary syndrome", "Sezary Lymphoma", "Sézary lymphoma", "Sezarys Lymphoma", "Syndrome, Sezary", "Sézary's disease", "Sezary's Disease", "SC)zary syndrome", "sezary's disease", "Sezary's disease", "sezary's syndrome", "Sezary's Lymphoma", "Sezary's syndrome", "Sézary's syndrome", "Sezary's lymphoma", "Lymphoma, Sezary's", "Sezary Erythroderma", "Sézary; reticulosis", "reticulosis; Sézary", "Erythroderma, Sezary", "CTCL / Sezary syndrome", "Sezary syndrome (diagnosis)", "Sézary's disease (disorder)", "RETICULOSIS SYNDROME, SEZARY", "Sézary disease, unspecified site", "Cutaneous T-cell lymphoma/Sezary syndrome", "cutaneous T-cell lymphoma/Sezary syndrome", "Sézary's disease (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sezary syndrome", "shortest_name_length": 2}
{"curie": "MONDO:0100059", "names": ["HEUS", "benign eosinophilia", "hypereosinophilia of undetermined significance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypereosinophilia of undetermined significance", "shortest_name_length": 4}
{"curie": "MONDO:0036217", "names": ["lethal pontocerebellar hypoplasia-hypotonia-respiratory insufficiency syndrome due to a point mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal pontocerebellar hypoplasia-hypotonia-respiratory insufficiency syndrome due to a point mutation", "shortest_name_length": 102}
{"curie": "MONDO:0013325", "names": ["CDG2I", "CDGIIi", "CDG IIi", "CDGIIdi", "CDG III", "CDG-IIi", "CDG-III", "COG5-CDG", "COG5-CDG (CDG-III)", "CDG syndrome type 3", "CDG syndrome type III", "CDG syndrome type IIi", "COG5 congenital disorder of glycosylation", "COG5-congenital disorder of glycosylation", "Congenital disorder of glycosylation type 2i", "congenital disorder of glycosylation type 2i", "congenital disorder of glycosylation type IIi", "congenital disorder of glycosylation type III", "Congenital disorder of glycosylation type IIi", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi", "congenital disorder of glycosylation, type III", "carbohydrate deficient glycoprotein syndrome type III", "Carbohydrate deficient glycoprotein syndrome type IIi", "CDG2I - carbohydrate deficient glycoprotein syndrome type IIi", "Component of oligomeric golgi complex 5 congenital disorder of glycosylation", "COG5 (component of oligomeric golgi complex 5) congenital disorder of glycosylation", "Component of oligomeric golgi complex 5 congenital disorder of glycosylation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "COG5-congenital disorder of glycosylation", "shortest_name_length": 5}
{"curie": "MONDO:0400000", "names": ["SIBO", "small intestinal bacterial overgrowth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small intestinal bacterial overgrowth", "shortest_name_length": 4}
{"curie": "MONDO:0006748", "names": ["Kojevnikov epilepsy", "Kojewnikow Syndrome", "kojewnikow syndrome", "Kojewnikov Epilepsy", "Kojevnikov Epilepsy", "Kozhevnikov Syndrome", "Kojevnikov's Epilepsy", "Kojevnikov's epilepsy", "kojevnikov's epilepsy", "Kojewnikov's Epilepsy", "Kojewnikow's Syndrome", "Kojewnikov's epilepsy", "Epilepsy, Kojevnikov's", "Kojewnikoff's syndrome", "Epilepsy, Kojewnikov's", "Kozhevnikov's Syndrome", "Kojevnikov's epilepsia", "Kojevnikov's Epilepsies", "Kozhevnikov's epilepsia", "Epilepsies, Kojevnikov's", "Focal status epilepticus", "Motor simple partial status", "Epilepsia Partialis Continua", "epilepsia partialis continua", "Epilepsia partialis continua", "Epilepsia partialis continua (disorder)", "epilepsia partialis continua (diagnosis)", "Epilepsia partialis continua [Kozhevnikof]", "Epilepsia partialis continua of Kojevnikov"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsia partialis continua", "shortest_name_length": 19}
{"curie": "MONDO:0030333", "names": ["IMD84", "IMMUNODEFICIENCY 84", "immunodeficiency 84", "immunodeficiency due to IKZF3 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 84", "shortest_name_length": 5}
{"curie": "UMLS:C3489571", "names": ["Familial Extrahepatic Biliary Atresia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Familial Extrahepatic Biliary Atresia", "shortest_name_length": 37}
{"curie": "MONDO:0001342", "names": ["dysgammaglobulinemia", "Dysgammaglobulinemia", "Dysgammaglobulinemias", "Dysgammaglobulinaemia", "dysgammaglobulinemia (disease)", "dysgammaglobulinemia (finding)", "Dysgammaglobulinemia (disorder)", "dysgammaglobulinemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dysgammaglobulinemia", "shortest_name_length": 20}
{"curie": "MONDO:0017008", "names": ["partial trisomy of chromosome X", "partial duplication of chromosome X", "partial duplication of chromosome type X"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of chromosome X", "shortest_name_length": 31}
{"curie": "UMLS:C4521611", "names": ["Stage IV Pleural Malignant Mesothelioma", "Stage IV Pleural Malignant Mesothelioma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Pleural Malignant Mesothelioma AJCC v8", "shortest_name_length": 39}
{"curie": "MONDO:0700093", "names": ["balanced Robertsonian translocation Down syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "balanced Robertsonian translocation Down syndrome", "shortest_name_length": 49}
{"curie": "UMLS:C0521508", "names": ["INJECTION SITE BRUISING", "Injection site bruising", "Injection site ecchymosis", "Ecchymosis injection site", "ECCHYMOSIS INJECTION SITE", "Injection site bruising (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site bruising", "shortest_name_length": 23}
{"curie": "MONDO:0021321", "names": ["Ca extrahepatic bile ducts", "extrahepatic bile duct cancer", "Extrahepatic bile duct cancer", "bile duct cancer, extrahepatic", "cancer of extrahepatic bile duct", "malignant extrahepatic bile duct tumor", "Malignant Extrahepatic Bile Duct Tumor", "Malignant Tumor of Extrahepatic Bile Duct", "Malignant Extrahepatic Bile Duct Neoplasm", "Malignant tumor of extrahepatic bile duct", "malignant extrahepatic bile duct neoplasm", "malignant tumor of extrahepatic bile duct", "Malignant tumour of extrahepatic bile duct", "Malignant Neoplasm of Extrahepatic Bile Duct", "malignant neoplasm of extrahepatic bile duct", "Malignant neoplasm of extrahepatic bile duct", "malignant tumor of the extrahepatic bile duct", "Malignant neoplasm of extrahepatic bile ducts", "Malignant Tumor of the Extrahepatic Bile Duct", "malignant neoplasm of the extrahepatic bile duct", "Malignant Neoplasm of the Extrahepatic Bile Duct", "Malignant neoplasm of extrahepatic bile ducts, NOS", "Malignant tumor of extrahepatic bile duct (disorder)", "malignant neoplasm of extrahepatic bile duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant tumor of extrahepatic bile duct", "shortest_name_length": 26}
{"curie": "UMLS:C3272258", "names": ["Severe Cardiac Valve Stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Severe Cardiac Valve Stenosis", "shortest_name_length": 29}
{"curie": "MONDO:0100328", "names": ["microcephaly, epilepsy, and diabetes syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly, epilepsy, and diabetes syndrome", "shortest_name_length": 45}
{"curie": "UMLS:C1336911", "names": ["Endometrial Endometrioid Adenocarcinoma with Small Glands, Tubules or Cords"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endometrial Endometrioid Adenocarcinoma with Small Glands, Tubules or Cords", "shortest_name_length": 75}
{"curie": "MONDO:0016878", "names": ["partial deletion of chromosome 16", "partial monosomy of chromosome 16", "partial deletion of chromosome type 16"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of chromosome 16", "shortest_name_length": 33}
{"curie": "UMLS:C2960634", "names": ["Hepatitis B reactivation", "reactivation of hepatitis B virus", "Reactivation of hepatitis B viral hepatitis", "reactivation of hepatitis B virus (diagnosis)", "Reactivation of hepatitis B viral hepatitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reactivation of hepatitis B viral hepatitis", "shortest_name_length": 24}
{"curie": "UMLS:C0855055", "names": ["Primary Fibrosarcoma", "Localized Fibrosarcoma", "Fibrosarcoma non-metastatic", "Non-Metastatic Fibrosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fibrosarcoma non-metastatic", "shortest_name_length": 20}
{"curie": "MONDO:0013026", "names": ["SMCD", "Subepithelial Mucinous Corneal Dystrophy", "Subepithelial mucinous corneal dystrophy", "SUBEPITHELIAL MUCINOUS CORNEAL DYSTROPHY", "subepithelial mucinous corneal dystrophy", "CORNEAL DYSTROPHY, SUBEPITHELIAL MUCINOUS", "Corneal Dystrophy, Subepithelial Mucinous", "corneal dystrophy, subepithelial mucinous", "Subepithelial mucinous corneal dystrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subepithelial mucinous corneal dystrophy", "shortest_name_length": 4}
{"curie": "UMLS:C4053796", "names": ["NSAID-Induced Nephropathy", "Non-steroidal Anti-inflammatory Drug-Induced Nephropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "NSAID-Induced Nephropathy", "shortest_name_length": 25}
{"curie": "UMLS:C0855264", "names": ["Unspecified Type Delusional Disorder", "Delusional disorder, unspecified type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Delusional disorder, unspecified type", "shortest_name_length": 36}
{"curie": "MONDO:0017498", "names": ["radio-ulnar terminal transverse meromelia, unilateral", "congenital absence of both forearm and hand, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital absence of both forearm and hand, unilateral", "shortest_name_length": 53}
{"curie": "UMLS:C4553701", "names": ["Stage IVB Uterine Corpus Cancer AJCC v8", "Stage IVB Uterine (including Endometrial) Cancer", "Stage IVB Uterine Corpus Carcinoma or Carcinosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Uterine Corpus Cancer AJCC v8", "shortest_name_length": 39}
{"curie": "UMLS:C5205658", "names": ["Locally Advanced Undifferentiated Pleomorphic Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Undifferentiated Pleomorphic Sarcoma", "shortest_name_length": 53}
{"curie": "UMLS:C1860446", "names": ["Bilateral congenital vertical talus", "Congenital vertical talus, bilateral", "Congenital vertical talus deformity of both ankles and feet", "Congenital vertical talus deformity of bilateral ankles and feet", "Congenital vertical talus deformity of bilateral ankles and feet (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bilateral congenital vertical talus", "shortest_name_length": 35}
{"curie": "MONDO:0041535", "names": ["Masshoff syndrome", "Masshoff's syndrome", "Masshoff's syndrome (disorder)", "Masshoff's syndrome (diagnosis)", "lymphadenitis mesenterialis Masshoff", "mesenteric lymphadenitis due to Yersinia infection", "Yersinia pseudotuberculosis mesenteric lymphadenitis", "Yersinia pseudotuberculosis caused mesenteric lymphadenitis", "mesenteric lymphadenitis due to Yersinia pseudotuberculosis", "Mesenteric lymphadenitis due to Yersinia pseudotuberculosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mesenteric lymphadenitis due to Yersinia infection", "shortest_name_length": 17}
{"curie": "UMLS:C0280159", "names": ["Stage III Grade 3 Follicular Lymphoma", "stage III grade 3 follicular lymphoma", "Grade III Follicular Lymphoma Stage III", "Follicular Lymphoma Grade III Stage III", "stage III follicular large cell lymphoma", "Stage III Follicular Large Cell Lymphoma", "Follicular Large Cell Lymphoma Stage III", "follicular large cell lymphoma, stage III", "Ann Arbor Stage III Grade 3 Follicular Lymphoma", "Grade III Follicular Large Cell Lymphoma Stage III", "Stage III Grade III Follicular Large Cell Lymphoma", "stage III grade III follicular large cell lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage III Grade 3 Follicular Lymphoma", "shortest_name_length": 37}
{"curie": "UMLS:C1518705", "names": ["Ovarian Dermoid Cyst with Secondary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Dermoid Cyst with Secondary Carcinoma", "shortest_name_length": 45}
{"curie": "MONDO:0043836", "names": ["tb spine", "spine tb", "TB spine", "Pott Disease", "POTT DISEASE", "pott disease", "disease pott", "Potts Disease", "potts disease", "diseases pott", "Potts disease", "disease, pott", "disease potts", "Disease, Pott", "pott's disease", "Pott's disease", "disease pott's", "Pott's Disease", "disease, pott's", "diseases pott's", "Disease, Pott's", "Tuberculous spine", "spine tuberculous", "pott's paraplegia", "tuberculosis spine", "spine tuberculosis", "Spinal Tuberculoses", "SPINE, TUBERCULOSIS", "Spinal Tuberculosis", "tuberculosis spinal", "Spine--Tuberculosis", "spinal Tuberculoses", "spinal tuberculosis", "Tuberculosis, Spinal", "tuberculosis, spinal", "Tuberculoses, Spinal", "Tuberculoses, spinal", "Tuberculosis of spine", "tuberculosis of spine", "Tuberculous spondylitis", "TUBERCULOUS SPONDYLITIS", "tuberculous spondylitis", "Pott; disease (etiology)", "SPONDYLITIS, TUBERCULOUS", "spinal cord tuberculosis", "Pott's disease (diagnosis)", "Tuberculosis of spinal cord", "Pott; disease (manifestation)", "Tuberculosis of spine (Pott's)", "tuberculosis of spine (pott's)", "Tuberculosis of vertebral column", "tuberculosis of vertebral column", "tuberculosis of spine (diagnosis)", "Tuberculosis of vertebral column - Pott's", "tuberculosis of vertebral column - pott's", "Tuberculosis of vertebral column (disorder)", "Tuberculosis of vertebral column, unspecified", "spine or vertebra; disorder, tuberculous (etiology)", "spine or vertebra; disorder, tuberculous (manifestation)", "Tuberculosis of vertebral column, unspecified examination", "disease (or disorder); spine or vertebra, tuberculous (etiology)", "disease (or disorder); spine or vertebra, tuberculous (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tuberculosis, spinal", "shortest_name_length": 8}
{"curie": "UMLS:C0405479", "names": ["Nipple disorder", "nipple disorder", "disorders nipple", "disorder of nipple", "Disorder of nipple", "Disorder of nipple (disorder)", "disorder of nipple (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disorder of nipple", "shortest_name_length": 15}
{"curie": "MONDO:0000599", "names": ["writing disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "writing disorder", "shortest_name_length": 16}
{"curie": "MONDO:0009268", "names": ["GD3C", "Gaucher-like disease", "Pseudo Gaucher disease", "pseudo Gaucher disease", "Gaucher disease type 3C", "Gaucher disease, type 3C", "Gaucher's disease type 3C", "Gaucher disease Type IIIC", "Gaucher disease, type IIIC", "GAUCHER DISEASE, TYPE IIIC", "Gaucher Disease, Type Iiic", "Gaucher's disease type IIIC", "Cardiovascular Gaucher disease", "cardiovascular Gaucher disease", "Gaucher disease Type IIIC (diagnosis)", "Gaucher disease - ophthalmoplegia - cardiovascular calcification", "Gaucher disease with ophthalmoplegia and cardiovascular calcification", "Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome", "Gaucher disease with ophthalmoplegia and cardiovascular calcification (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0013482", "names": ["MKS8", "Meckel syndrome 8", "TCTN2 Meckel syndrome", "Meckel syndrome type 8", "Meckel syndrome, type 8", "MECKEL SYNDROME, TYPE 8", "Meckel-Gruber syndrome, type 8", "Meckel syndrome type 8 (diagnosis)", "Meckel syndrome caused by mutation in TCTN2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meckel syndrome, type 8", "shortest_name_length": 4}
{"curie": "UMLS:C4544822", "names": ["dMMR colorectal cancer", "MSI-H colorectal cancer", "Mismatch repair deficient colorectal cancer", "colorectal cancer microsatellite instability-high", "Microsatellite instability-high colorectal cancer", "Microsatellite instability-high colorectal cancer (disorder)", "Microsatellite instability-high colorectal cancer (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Microsatellite instability-high colorectal cancer", "shortest_name_length": 22}
{"curie": "UMLS:C0555307", "names": ["Colon injury", "Colon Injury", "injury colon", "colon injury", "colon; injury", "injury; colon", "colon injuries", "injury of colon", "Injury of colon", "COLON NOS INJURY", "injury; bowel, large", "injury of large intestine", "Injury of large intestine", "Injury of colon (disorder)", "injury of colon (diagnosis)", "Injury of large intestine (disorder)", "injury of large intestine (diagnosis)", "injury to gastrointestinal tract large intestine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of colon", "shortest_name_length": 12}
{"curie": "MONDO:0006221", "names": ["adenoma gastric", "Gastric Adenoma", "stomach adenoma", "gastric adenoma", "Gastric adenoma", "Adenoma of Stomach", "adenoma of stomach", "Adenoma of the Stomach", "benign gastric adenoma", "adenoma of the stomach", "adenoma of stomach (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric adenoma", "shortest_name_length": 15}
{"curie": "UMLS:C3272479", "names": ["Ampulla of Vater Neuroendocrine Tumor G2", "Neuroendocrine Tumor G2 of the Ampullary Region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ampulla of Vater Neuroendocrine Tumor G2", "shortest_name_length": 40}
{"curie": "UMLS:C0278512", "names": ["metastatic osteosarcoma", "Metastatic Osteosarcoma", "Osteosarcoma metastatic", "Metastatic osteosarcoma", "osteosarcoma, metastatic", "Osteosarcoma, Metastatic", "Metastatic Osteogenic Sarcoma", "metastatic osteogenic sarcoma", "Osteogenic sarcoma metastatic", "osteogenic sarcoma, metastatic", "sarcoma, metastatic osteogenic", "Metastatic osteosarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic osteosarcoma", "shortest_name_length": 23}
{"curie": "UMLS:C0854142", "names": ["aorta; thrombosis", "Aortic thrombosis", "aortic thrombosis", "thrombosis; aortic", "thrombosis of aorta", "Thrombosis of aorta", "aortic artery thrombosis", "Thrombosis of aorta (disorder)", "thrombosis of aorta (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thrombosis of aorta", "shortest_name_length": 17}
{"curie": "UMLS:C3899637", "names": ["Unfavorable Prognosis Hodgkin Lymphoma", "childhood unfavorable prognosis Hodgkin lymphoma", "Childhood Unfavorable Prognosis Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Unfavorable Prognosis Hodgkin Lymphoma", "shortest_name_length": 38}
{"curie": "MONDO:0017948", "names": ["HCHWA, Flemish type", "ABetaA21G amyloidosis", "ABetaA21G-related amyloidosis", "ABeta amyloidosis, Flemish type", "cerebral amyloid angiopathy, APP-related, Flemish variant", "hereditary cerebral hemorrhage with amyloidosis, Flemish type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ABetaA21G amyloidosis", "shortest_name_length": 19}
{"curie": "MONDO:0002666", "names": ["Signet ring cell carcinoma", "pancreas signet ring cell carcinoma", "pancreatic signet Ring cell carcinoma", "Pancreatic Signet-Ring Cell Carcinoma", "pancreatic signet ring cell carcinoma", "Pancreatic Signet Ring Cell Carcinoma", "signet Ring cell carcinoma of pancreas", "signet ring cell carcinoma of pancreas", "Signet Ring Cell Carcinoma of Pancreas", "Signet Ring cell carcinoma of pancreas", "signet Ring cell carcinoma of the pancreas", "pancreatic signet ring cell adenocarcinoma", "Signet Ring Cell Carcinoma of the Pancreas", "signet ring cell carcinoma of pancreas (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic signet ring cell adenocarcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0013364", "names": ["RSTS2", "RUBINSTEIN-TAYBI SYNDROME 2", "Rubinstein-Taybi syndrome 2", "EP300 Rubinstein-Taybi syndrome", "Rubinstein-Taybi Syndrome Type 2", "Rubinstein-Taybi syndrome type 2", "Rubinstein-Taybi syndrome caused by mutation in EP300", "Rubinstein-Taybi syndrome due to EP300 haploinsufficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rubinstein-Taybi syndrome due to EP300 haploinsufficiency", "shortest_name_length": 5}
{"curie": "MONDO:0011773", "names": ["ANXD", "ANXD1", "Anauxetic dysplasia", "anauxetic dysplasia", "ANAUXETIC DYSPLASIA", "anauxetic dysplasia 1", "anauxetic dysplasia type 1", "Spondyloepimetaphyseal dysplasia Menger type", "spondylometaepiphyseal dysplasia Menger type", "spondylometaepiphyseal dysplasia, Menger type", "Spondylometaepiphyseal dysplasia, Menger type", "SPONDYLOMETAEPIPHYSEAL DYSPLASIA, MENGER TYPE", "spondyloepimetaphyseal dysplasia, Menger type", "Spondyloepimetaphyseal dysplasia, Menger type", "spondylometaepiphyseal dysplasia anauxetic type", "spondyloepimetaphyseal dysplasia anauxetic type", "Spondyloepimetaphyseal dysplasia anauxetic type", "SPONDYLOEPIMETAPHYSEAL DYSPLASIA, ANAUXETIC TYPE", "spondyloepimetaphyseal dysplasia, anauxetic type", "spondylometaepiphyseal dysplasia, anauxetic type", "Spondylometaepiphyseal dysplasia, Anauxetic type", "SPONDYLOMETAEPIPHYSEAL DYSPLASIA, ANAUXETIC TYPE", "Spondyloepimetaphyseal dysplasia, anauxetic type", "Spondyloepimetaphyseal dysplasia anauxetic type (disorder)", "spondyloepimetaphyseal dysplasia anauxetic type (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anauxetic dysplasia", "shortest_name_length": 4}
{"curie": "MONDO:0009842", "names": ["IMD108", "immunodeficiency 108 with autoinflammation", "IMMUNODEFICIENCY 108 WITH AUTOINFLAMMATION", "Pelger-Huet-Like Anomaly and Episodic Fever with Abdominal Pain", "PELGER-HUET-LIKE ANOMALY AND EPISODIC FEVER WITH ABDOMINAL PAIN", "Pelger-Huet-like anomaly and episodic fever with abdominal pain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pelger-Huet-like anomaly and episodic fever with abdominal pain", "shortest_name_length": 6}
{"curie": "MONDO:0009934", "names": ["ACDMPV", "ACD MPV", "ACD-MPV", "Fetal circulation", "fetal circulation", "circulation; fetal", "fetal; circulation", "Persistent fetal circulation", "alveolar capillary dysplasia", "persistent fetal circulation", "Alveolar/capillary dysplasia", "Persistent Fetal Circulation", "Alveolar capillary dysplasia", "Alveolar Capillary Dysplasia", "fetal; persistent circulation", "FETAL CIRCULATION, PERSISTENT", "persistent foetal circulation", "Persistent foetal circulation", "Circulation, Persistent Fetal", "persistent; fetal circulation", "Fetal Circulation, Persistent", "circulation; fetal persistent", "fetal; circulation, persistent", "persistent; circulation, fetal", "PFC - Persistent fetal circulation", "PFC - Persistent foetal circulation", "Misalignment of the Pulmonary Vessels", "Persistent Fetal Circulation Syndrome", "persistent fetal circulation syndrome", "Persistent fetal circulation syndrome", "Persistent foetal circulation syndrome", "Persistent fetal circulation disorders", "persistent foetal circulation syndrome", "Congenital alveolar capillary dysplasia", "Persistent foetal circulation disorders", "congenital alveolar capillary dysplasia", "persistent fetal circulation (diagnosis)", "Newborn persistent pulmonary hypertension", "Persistent pulmonary hypertension of newborn", "Persistent Pulmonary Hypertension of Newborn", "persistent pulmonary hypertension of newborn", "Hypertension, Pulmonary, of Newborn, Persistent", "Persistent pulmonary hypertension of the newborn", "persistent pulmonary hypertension of the newborn", "Congenital pulmonary alveolar capillary dysplasia", "PPHN - Persistent pulmonary hypertension in newborn", "persistent pulmonary hypertension of newborn (diagnosis)", "familial persistent pulmonary hypertension of the newborn", "Familial Persistent Pulmonary Hypertension of the Newborn", "pulmonary hypertension, familial persistent of the newborn", "Pulmonary Hypertension, Familial Persistent, of the Newborn", "Persistent pulmonary hypertension of the newborn (disorder)", "Congenital pulmonary alveolar capillary dysplasia (disorder)", "Alveolar capillary dysplasia with pulmonary venous misalignment", "alveolar capillary dysplasia with pulmonary venous misalignment", "Alveolar Capillary Dysplasia With Misalignment Of Pulmonary Veins", "Alveolar capillary dysplasia with misalignment of pulmonary veins", "alveolar capillary dysplasia with misalignment of pulmonary veins", "ALVEOLAR CAPILLARY DYSPLASIA WITH MISALIGNMENT OF PULMONARY VEINS", "Alveolar capillary dysplasia with misalignment of pulmonary vessels", "alveolar capillary dysplasia with misalignment of pulmonary vessels", "Alveolar capillary dysplasia with pulmonary venous misalignment (disorder)", "congenital alveolar capillary dysplasia with misalignment of pulmonary veins", "ALVEOLAR CAPILLARY DYSPLASIA WITH MISALIGNMENT OF PULMONARY VEINS AND OTHER CONGENITAL ANOMALIES", "alveolar capillary dysplasia with misalignment of pulmonary veins and other congenital anomalies", "alveolar capillary dysplasia with misalignment of pulmonary veins and Other congenital anomalies", "Alveolar Capillary Dysplasia With Misalignment Of Pulmonary Veins And Other Congenital Anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alveolar capillary dysplasia with misalignment of pulmonary veins", "shortest_name_length": 6}
{"curie": "UMLS:C5206795", "names": ["Advanced Cholangiocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Cholangiocarcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0006812", "names": ["intracranial vasospasm", "Intracranial Vasospasm", "Intracranial Angiospasm", "Vasospasm, Intracranial", "Intracranial Vasospasms", "Intracranial Angiospasms", "Vasospasms, Intracranial", "Angiospasm, Intracranial", "Angiospasms, Intracranial", "Intracranial Vascular Spasm", "Intracranial Vascular Spasms", "Vascular Spasm, Intracranial", "Spasm, Intracranial Vascular", "Vascular Spasms, Intracranial", "Spasms, Intracranial Vascular"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intracranial vasospasm", "shortest_name_length": 22}
{"curie": "UMLS:C0280348", "names": ["Stage II Lip and Oral Cavity Squamous Cell Cancer", "Stage II Lip and Oral Cavity Squamous Cell Carcinoma", "lip and oral cavity squamous cell carcinoma, stage II", "oral cavity and lip squamous cell carcinoma, stage II", "epidermoid carcinoma of the lip and oral cavity, stage II", "stage II squamous cell carcinoma of the lip and oral cavity", "Stage II Lip and Oral Cavity Squamous Cell Carcinoma AJCC v6", "squamous cell carcinoma of the lip and oral cavity, stage II", "Stage II Lip and Oral Cavity Squamous Cell Carcinoma AJCC v7", "Stage II Lip and Oral Cavity Squamous Cell Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Lip and Oral Cavity Squamous Cell Carcinoma AJCC v6 and v7", "shortest_name_length": 49}
{"curie": "UMLS:C0149976", "names": ["Proctitis herpes", "herpes proctitis", "proctitis herpes", "PROCTITIS HERPES", "PROCTITIS, HERPES", "Herpes simplex anorectal", "herpes; proctitis (etiology)", "proctitis; herpetic (etiology)", "herpes; proctitis (manifestation)", "proctitis; herpetic (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Proctitis herpes", "shortest_name_length": 16}
{"curie": "UMLS:C0585059", "names": ["Displaced fracture", "displaced fracture", "fracture displaced", "displaced fractures", "fracture displacement", "Fracture displacement", "Fracture with displacement", "Fracture with displacement (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fracture with displacement", "shortest_name_length": 18}
{"curie": "UMLS:C3544265", "names": ["Recurrent Intrahepatic Cholangiocarcinoma", "Intrahepatic cholangiocarcinoma recurrent", "Recurrent Intrahepatic Bile Duct Cancer (Cholangiocarcinoma)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intrahepatic cholangiocarcinoma recurrent", "shortest_name_length": 41}
{"curie": "MONDO:0020728", "names": ["RHUC1", "renal hypouricemia", "RENAL HYPOURICEMIA", "Renal hypouricemia", "Hypouricemia, renal", "hypouricemia, renal", "hypouricemia, renal 1", "HYPOURICEMIA, RENAL, 1", "Hypouricemia, Renal, 1", "Dalmatian hypouricemia", "hypouricemia, renal, 1", "DALMATIAN HYPOURICEMIA", "Dalmatian hypouricaemia", "hypouricemia, renal, type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypouricemia, renal 1", "shortest_name_length": 5}
{"curie": "UMLS:C2931844", "names": ["Spinal muscular atrophy 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spinal muscular atrophy 4", "shortest_name_length": 25}
{"curie": "MONDO:0003186", "names": ["esophageal adenoid cystic cancer", "Esophageal Adenoid Cystic Cancer", "Adenoid Cystic Esophagus Carcinoma", "Esophagus Adenoid Cystic Carcinoma", "esophagus adenoid cystic carcinoma", "adenoid cystic esophagus carcinoma", "adenoid cystic carcinoma, esophagus", "Esophageal Adenoid Cystic Carcinoma", "Adenoid Cystic Carcinoma, Esophagus", "esophageal adenoid cystic carcinoma", "Adenoid Cystic Carcinoma of Esophagus", "adenoid cystic carcinoma of esophagus", "adenoid cystic carcinoma of the esophagus", "Adenoid Cystic Carcinoma of the Esophagus", "adenoid cystic carcinoma of esophagus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophageal adenoid cystic carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0022311", "names": ["cote katsantoni syndrome", "Cote Katsantoni syndrome", "ectodermal dysplasia osteosclerosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cote katsantoni syndrome", "shortest_name_length": 24}
{"curie": "MONDO:0800183", "names": ["PAX6-related ocular dysgenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PAX6-related ocular dysgenesis", "shortest_name_length": 30}
{"curie": "UMLS:C5554631", "names": ["Recurrent WHO Grade I Glioma", "Recurrent WHO Grade 1 Glioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent WHO Grade 1 Glioma", "shortest_name_length": 28}
{"curie": "MONDO:0035651", "names": ["choanal atresia-athelia-hypothyroidism-delayed puberty-short stature syndrome", "KMT2D-related choanal atresia-athelia-hypothyroidism-delayed puberty-short stature syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choanal atresia-athelia-hypothyroidism-delayed puberty-short stature syndrome", "shortest_name_length": 77}
{"curie": "UMLS:C1332234", "names": ["Alkylating Agent-Related AML and MDS", "AML and myelodysplastic syndromes related to alkylating agent", "Alkylating Agent Related Acute Myeloid Leukemia and Myelodysplastic Syndrome", "Alkylating Agent-Related Acute Myeloid Leukemia and Myelodysplastic Syndrome", "Acute myeloid leukemia and myelodysplastic syndrome related to alkylating agent", "Acute myeloid leukaemia and myelodysplastic syndrome related to alkylating agent", "Acute myeloid leukemia and myelodysplastic syndromes related to alkylating agent", "Acute myeloid leukemia and myelodysplastic syndrome related to alkylating agent (disorder)", "Acute myeloid leukemia and myelodysplastic syndrome related to alkylating agent (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute myeloid leukemia and myelodysplastic syndrome related to alkylating agent", "shortest_name_length": 36}
{"curie": "UMLS:C0279962", "names": ["Stage I Lymphoblastic Lymphoma", "Stage I Adult Lymphoblastic Lymphoma", "Adult Stage I Lymphoblastic Lymphoma", "Adult Lymphoblastic Lymphoma Stage I", "stage I adult lymphoblastic lymphoma", "adult lymphoblastic lymphoma, stage I", "Ann Arbor Stage I Adult Lymphoblastic Lymphoma", "Stage I Adult Precursor Lymphoblastic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Adult Lymphoblastic Lymphoma", "shortest_name_length": 30}
{"curie": "MONDO:0034669", "names": ["non-syndromic preaxial polydactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-syndromic preaxial polydactyly", "shortest_name_length": 34}
{"curie": "MONDO:0016475", "names": ["Beckwith-Wiedemann syndrome due to imprinting defect of 11p15", "Beckwith-Wiedemann syndrome due to imprinting defect of type 11p15"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Beckwith-Wiedemann syndrome due to imprinting defect of 11p15", "shortest_name_length": 61}
{"curie": "UMLS:C4683410", "names": ["Differentiated Thyroid Gland Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Differentiated Thyroid Gland Carcinoma by AJCC v7 Stage", "shortest_name_length": 55}
{"curie": "MONDO:0010292", "names": ["Fcms", "FCMS", "FCMSU", "URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME", "Uruguay faciocardiomusculoskeletal syndrome", "URUGUAY FACIOCARDIOMUSCULOSKELETAL syndrome", "Uruguay Faciocardiomusculoskeletal Syndrome", "Uruguay Faciocardiomusculoskeletal syndrome", "faciocardiomusculoskeletal syndrome, Uruguay type", "FACIOCARDIOMUSCULOSKELETAL SYNDROME, URUGUAY TYPE", "Faciocardiomusculoskeletal Syndrome, Uruguay Type", "uruguay faciocardiomusculoskeletal syndrome, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uruguay Faciocardiomusculoskeletal syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C2981381", "names": ["Stage IIIB Small Intestinal Cancer", "Stage IIIB Small Intestinal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Small Intestinal Cancer AJCC v7", "shortest_name_length": 34}
{"curie": "MONDO:0003795", "names": ["SCCO", "ovarian small cell NEC", "Ovarian Small Cell Cancer", "ovarian small cell cancer", "ovary small cell carcinoma", "small cell ovarian carcinoma", "Ovarian Small Cell Carcinoma", "Small cell ovarian carcinoma", "ovarian small cell carcinoma", "Small cell carcinoma of ovary", "small cell carcinoma of ovary", "small cell carcinoma of the ovary", "Small cell carcinoma of the ovary", "Small cell carcinoma of ovary (disorder)", "small cell carcinoma of ovary (diagnosis)", "ovarian small cell neuroendocrine carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian small cell carcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0008359", "names": ["radio-renal syndrome", "Radio-renal syndrome", "Radio renal syndrome", "radio renal syndrome", "RADIAL-RENAL SYNDROME", "radial-renal syndrome", "Radio-renal syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radio-renal syndrome", "shortest_name_length": 20}
{"curie": "UMLS:C3273727", "names": ["Breast Solid Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Solid Neuroendocrine Carcinoma", "shortest_name_length": 37}
{"curie": "UMLS:C5556690", "names": ["Unresectable Gastroesophageal Junction Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Gastroesophageal Junction Neuroendocrine Carcinoma", "shortest_name_length": 63}
{"curie": "MONDO:0003610", "names": ["rete ovarii cystadenoma", "Rete Ovarii Cystadenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rete ovarii cystadenoma", "shortest_name_length": 23}
{"curie": "UMLS:C0042033", "names": ["Female urogenital fistula", "Female Urogenital Fistula", "Urogenital fistula (female)", "Female Genitourinary Fistula", "Female urogenital fistula, NOS", "Female urinary-genital tract fistula", "female urinary-genital tract fistula", "Urinary-genital tract fistula, female", "Urinary-genital tract fistulae, female", "Female urinary-genital tract fistula, NOS", "fistula involving female urinary genital tract", "Female urinary-genital tract fistula (disorder)", "female urinary-genital tract fistula (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Female urinary-genital tract fistula", "shortest_name_length": 25}
{"curie": "UMLS:C0280374", "names": ["oropharynx squamous cell carcinoma, stage IV", "Oropharyngeal squamous cell carcinoma stage IV", "oropharynx squamous cell carcinoma, metastatic", "oropharyngeal squamous cell carcinoma, stage IV", "Metastatic Oropharyngeal Squamous Cell Carcinoma", "epidermoid carcinoma of the oropharynx, stage IV", "oropharyngeal squamous cell carcinoma, metastatic", "stage IV squamous cell carcinoma of the oropharynx", "epidermoid carcinoma of the oropharynx, metastatic", "squamous cell carcinoma of the oropharynx, stage IV", "Metastatic Oropharyngeal Throat Squamous Cell Cancer", "metastatic squamous cell carcinoma of the oropharynx", "Metastatic Squamous Cell Carcinoma of the Oropharynx", "squamous cell carcinoma of the oropharynx, metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Squamous Cell Carcinoma of the Oropharynx", "shortest_name_length": 44}
{"curie": "MONDO:0018047", "names": ["Familial thrombomodulin anomalies", "familial thrombomodulin anomalies", "thrombomodulin anomalies, familial", "Thrombomodulin anomalies, familial", "Familial thrombomodulin anomalies (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial thrombomodulin anomalies", "shortest_name_length": 33}
{"curie": "UMLS:C5557435", "names": ["Deafness due to Connexin 26 Gene Anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Deafness due to Connexin 26 Gene Anomaly", "shortest_name_length": 40}
{"curie": "MONDO:0013414", "names": ["RP44", "RETINITIS PIGMENTOSA 44", "retinitis pigmentosa 44", "RGR retinitis pigmentosa", "retinitis pigmentosa type 44", "retinitis pigmentosa caused by mutation in RGR"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 44", "shortest_name_length": 4}
{"curie": "UMLS:C1333937", "names": ["Hard Palate Monomorphic Adenoma", "Monomorphic Adenoma of Hard Palate", "Monomorphic Adenoma of the Hard Palate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hard Palate Monomorphic Adenoma", "shortest_name_length": 31}
{"curie": "OMIM:133600", "names": ["Heel exostosis", "Exostoses Of Heel", "EXOSTOSES OF HEEL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 14}
{"curie": "MONDO:0011956", "names": ["AUTS3", "AUTISM, SUSCEPTIBILITY TO, 3", "autism, susceptibility to, 3", "autism susceptibility 3, isolated cases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autism, susceptibility to, 3", "shortest_name_length": 5}
{"curie": "UMLS:C0877440", "names": ["Periorbital erythema", "Erythema periorbital", "Periorbital erythema (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Periorbital erythema", "shortest_name_length": 20}
{"curie": "UMLS:C5420050", "names": ["Sinonasal Synovial Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Synovial Sarcoma", "shortest_name_length": 26}
{"curie": "MONDO:0005825", "names": ["Gikiyami", "Mud fever", "mud fever", "fever; mud", "Nanukayami", "nanukayami", "mud; fever", "Swamp fever", "swamp fever", "Fever, swamp", "Weil disease", "Weil Disease", "LEPTOSPIROSIS", "harvest fever", "leptospiroses", "leptospirosis", "Leptospirosis", "Leptospiroses", "Harvest fever", "Weil's disease", "canicola fever", "Seven-day fever", "seven day fever", "seven-day fever", "Red water fever", "red water fever", "Seven day fever", "fever; seven-day", "FEVER, SEVEN DAY", "rice-field fever", "fort Bragg fever", "Queensland fever", "fort bragg fever", "Nanukayami fever", "Fort Bragg fever", "queensland fever", "seven-day; fever", "nanukayami fever", "fever; Queensland", "Stuttgart disease", "Queensland; fever", "cane-cutter fever", "Stuttgart Disease", "Leptospirosis, NOS", "Nanukayami disease", "swineherd's disease", "Cane cutter's fever", "cane cutter's fever", "Spirochetal jaundice", "hemorrhagic jaundice", "spirochetal jaundice", "Leptospira Infection", "Infection, Leptospira", "Leptospira infections", "Leptospira Infections", "spirochaetal jaundice", "Nanukayami (disorder)", "Spirochaetal jaundice", "rat catcher's yellows", "Rat Catcher's Yellows", "leptospiral; infection", "infection; leptospiral", "Infections, Leptospira", "japanese autumnal fever", "Icterohemorrhagic fever", "Japanese autumnal fever", "Leptospirosis (disorder)", "leptospirosis (diagnosis)", "swamp fever; leptospirosis", "Leptospirosis, unspecified", "swamp; fever, leptospirosis", "Infection due to Leptospira", "infection due to Leptospira", "fever; swamp, leptospirosis", "rice-field worker's disease", "Rice-field worker's disease", "Leptospira infectious disease", "Leptospira disease or disorder", "Infection due to Leptospira, NOS", "leptospirosis icterohaemorrhagica", "Leptospirosis icterohaemorrhagica", "Leptospira caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leptospirosis", "shortest_name_length": 8}
{"curie": "MONDO:0019799", "names": ["HEP", "Erythrohepatic Porphyria", "Porphyria, Erythrohepatic", "Erythrohepatic Porphyrias", "Porphyrias, Erythrohepatic", "Hepatoerythropoietic Porphyria", "Hepatoerythropoietic porphyria", "hepatoerythropoietic porphyria", "Hepatoerythropoietic Porphyrias", "Porphyria, Hepatoerythropoietic", "PORPHYRIA, HEPATOERYTHROPOIETIC", "Porphyrias, Hepatoerythropoietic", "Homozygous porphyria cutanea tarda", "Homozygous porphyria cutanea tarda (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatoerythropoietic porphyria", "shortest_name_length": 3}
{"curie": "MONDO:0043133", "names": ["microcephaly micropenis seizures", "Microcephaly micropenis seizures", "Microcephaly micropenis convulsions", "microcephaly micropenis convulsions", "Microcephaly seizures genital hypoplasia", "microcephaly seizures genital hypoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly micropenis convulsions", "shortest_name_length": 32}
{"curie": "MONDO:0032859", "names": ["SPGF40", "spermatogenic failure 40", "SPERMATOGENIC FAILURE 40"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 40", "shortest_name_length": 6}
{"curie": "MONDO:0010830", "names": ["EPMR", "CLN8", "CLN8 disease", "NORTHERN EPILEPSY", "Northern epilepsy", "Northern epilepsy syndrome", "NCL, Northern epilepsy variant", "Neuronal ceroid lipofuscinosis 8", "neuronal ceroid lipofuscinosis 8", "Ceroid lipofuscinosis, neuronal 8", "Ceroid Lipofuscinosis, Neuronal, 8", "CEROID LIPOFUSCINOSIS, NEURONAL, 8", "ceroid lipofuscinosis, neuronal, 8", "CLN8 neuronal ceroid lipofuscinosis", "neuronal ceroid lipofuscinosis type 8", "CLN8 disease, Northern epilepsy variant", "ceroid lipofuscinosis, neuronal, type 8", "Epilepsy progressive with mental retardation", "Progressive epilepsy with mental retardation", "Epilepsy, Progressive, With Mental Retardation", "EPILEPSY, PROGRESSIVE, WITH MENTAL RETARDATION", "neuronal ceroid lipofuscinosis caused by mutation in CLN8", "Neuronal ceroid lipofuscinosis, Northern epilepsy variant", "Ceroid Lipofuscinosis, Neuronal, 8, Northern Epilepsy Variant", "CEROID LIPOFUSCINOSIS, NEURONAL, 8, NORTHERN EPILEPSY VARIANT", "Progressive epilepsy-intellectual disability syndrome Finnish type", "progressive epilepsy-intellectual disability syndrome, Finnish type", "Progressive epilepsy-intellectual disability syndrome, Finnish type", "Progressive epilepsy-intellectual disability syndrome Finnish type (disorder)", "progressive epilepsy-intellectual disability syndrome, Finnish type (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuronal ceroid lipofuscinosis 8", "shortest_name_length": 4}
{"curie": "UMLS:C1301526", "names": ["CLARE", "Overwear Syndrome", "Overwear syndrome", "Immobile Lens Syndrome", "Contact lens overwear syndrome", "Contact Lens Overwear Syndrome", "Contact Lens-induced Acute Red Eye", "Contact lens overwear syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Contact lens overwear syndrome (disorder)", "shortest_name_length": 5}
{"curie": "MONDO:0004103", "names": ["Tall Cell Variant Papillary Carcinoma", "tall cell variant papillary carcinoma", "Tall Cell Variant Thyroid Gland Papillary Carcinoma", "tall cell variant thyroid gland papillary carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tall cell variant thyroid gland papillary carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0054738", "names": ["FRASRS2", "Fraser syndrome 2", "FRASER SYNDROME 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fraser syndrome 2", "shortest_name_length": 7}
{"curie": "MONDO:0016285", "names": ["cervical papillary carcinoma", "uterine cervix papillary carcinoma", "papillary carcinoma of the cervix uteri"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papillary carcinoma of the cervix uteri", "shortest_name_length": 28}
{"curie": "EFO:0009275", "names": ["premature cardiac contractions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "premature cardiac contractions", "shortest_name_length": 30}
{"curie": "UMLS:C0261486", "names": ["Accidental poisoning by lead and its compounds and fumes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Accidental poisoning by lead and its compounds and fumes", "shortest_name_length": 56}
{"curie": "UMLS:C4744307", "names": ["Extremity Sarcoma", "Sarcoma of the Extremity", "Primary Extremity Sarcoma", "Primary Sarcoma of the Extremity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sarcoma of the Extremity", "shortest_name_length": 17}
{"curie": "UMLS:C1335101", "names": ["Occupational Cancer", "Occupational Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Occupational Malignant Neoplasm", "shortest_name_length": 19}
{"curie": "UMLS:C1710055", "names": ["SERIOUS INJURY", "Serious Injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Serious Injury", "shortest_name_length": 14}
{"curie": "MONDO:0007488", "names": ["LBD", "DLB", "Lewy Body", "Lewy body", "body lewi", "lewy body", "body lewis", "bodys lewy", "lewy bodies", "Lewy Bodies", "bodies lewy", "Lewy bodies", "bodies lewi", "bodies lewis", "body disease lewy", "lewy body disease", "Lewy body disease", "Lewy Body Disease", "body disease lewi", "LEWY BODY DEMENTIA", "body diseases lewy", "Lewy body dementia", "body lewy dementia", "Lewy Body Dementia", "body dementia lewy", "body disease lewis", "body dementia lewi", "lewy body dementia", "Dementia, Lewy Body", "DEMENTIA, LEWY BODY", "bodies disease lewy", "dementia, Lewy body", "body dementia lewis", "lewy bodies dementia", "dementia lewy bodies", "bodies dementia lewy", "bodies dementias lewy", "LBD - Lewy body disease", "Dementia with lewy bodies", "Diffuse Lewy body disease", "diffuse Lewy body disease", "diffuse lewy body disease", "Diffuse Lewy Body Disease", "Senile Lewy body dementia", "Dementia with Lewy bodies", "Dementia with Lewy Bodies", "dementia with Lewy bodies", "DIFFUSE LEWY BODY DISEASE", "dementia with lewy bodies", "cortical Lewy body disease", "Cortical Lewy body disease", "Lewy Body Disease, Diffuse", "Cortical Lewy Body Disease", "Lewy Body Disease, Cortical", "Dementia of the Lewy body type", "Lewy Body Type Senile Dementia", "DLBD - Diffuse Lewy body disease", "senile dementia with Lewy bodies", "CLBD - Cortical Lewy body disease", "Diffuse Lewy body disease (disorder)", "dementia with Lewy bodies (diagnosis)", "lewy body dementia, susceptibility to", "Lewy bodies (morphologic abnormality)", "Senile dementia of the Lewy body type", "Lewy body variant of Alzheimer disease", "Lewy Body Variant of Alzheimer Disease", "LEWY BODY VARIANT OF ALZHEIMER DISEASE", "SDLT - senile dementia of Lewy body type", "Lewy body variant of Alzheimer's disease", "diffuse Lewy body disease with gaze palsy", "DIFFUSE LEWY BODY DISEASE WITH GAZE PALSY", "Diffuse Lewy Body Disease with Gaze Palsy", "senile dementia with Lewy bodies (diagnosis)", "SDLT - Senile dementia of the Lewy body type", "Senile dementia of the Lewy body type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lewy body dementia", "shortest_name_length": 3}
{"curie": "MONDO:0100386", "names": ["AML, t(v;11q23.3)", "AML, t(V;11)(v;q23)", "AML, t(11;v)(q23;v)", "AML, t(V;11)(v;q23.3)", "AML, t(11;v)(q23.3;v)", "AML, 11q23.3 Translocation", "acute myeloid leukemia, t(v;11q23.3)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, t(v;11q23.3)", "shortest_name_length": 17}
{"curie": "UMLS:C1285445", "names": ["Substance-induced sleep disorder", "Substance-Induced Sleep Disorder", "Substance-induced sleep disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Substance-induced sleep disorder", "shortest_name_length": 32}
{"curie": "MONDO:0008818", "names": ["ATS", "ATORS", "Arterial Tortuosity", "ARTERIAL TORTUOSITY", "arterial tortuosity", "ARTERIAL TORTUOSITY SYNDROME", "Arterial Tortuosity Syndrome", "Arterial tortuosity syndrome", "arterial tortuosity syndrome", "Arterial tortuosity syndrome (disorder)", "Arterial tortuosity syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arterial tortuosity syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0015962", "names": ["genetic renal tubular disease", "inherited renal tubular disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited renal tubular disease", "shortest_name_length": 29}
{"curie": "UMLS:C3661485", "names": ["17p11.2 Monosomy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "17p11.2 Monosomy", "shortest_name_length": 16}
{"curie": "MONDO:0700169", "names": ["canine cutaneous t-cell lymphoma", "Canine Cutaneous T-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canine cutaneous t-cell lymphoma", "shortest_name_length": 32}
{"curie": "UMLS:C0346997", "names": ["Metastasis to vagina", "Metastasis to Vagina", "Metastases to vagina", "Metastasis to the Vagina", "Secondary Tumor to Vagina", "Secondary tumor to vagina", "Secondary tumour to vagina", "Cancer metastatic to vagina", "Secondary Tumor to the Vagina", "Metastatic Neoplasm to the Vagina", "Vaginal neoplasm malignant stage IVB", "vaginal neoplasm malignant secondary", "Vaginal neoplasm malignant metastatic", "Malignant neoplasm of vagina stage IVB", "Secondary malignant neoplasm of vagina", "Malignant neoplasm of vagina metastatic", "Metastatic malignant neoplasm of vagina", "Metastatic malignant neoplasm to vagina", "metastasis of malignant neoplasm to vagina", "Metastatic Malignant Neoplasm to the Vagina", "Metastatic Malignant Neoplasm in the Vagina", "Secondary malignant neoplasm of vagina, NOS", "Metastatic malignant neoplasm to vagina, NOS", "Secondary malignant neoplasm of vagina (diagnosis)", "Metastatic malignant neoplasm to vagina (disorder)", "metastasis of malignant neoplasm to vagina (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to vagina", "shortest_name_length": 20}
{"curie": "UMLS:C4284040", "names": ["FIGO Stage III Ovarian Cancer", "FIGO Stage III Ovarian Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Stage III Ovarian Cancer", "shortest_name_length": 29}
{"curie": "MONDO:0100241", "names": ["inherited thrombocytopenia", "hereditary thrombocytopenia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited thrombocytopenia", "shortest_name_length": 26}
{"curie": "UMLS:C0969675", "names": ["Uniparental heterodisomy", "Uniparental Heterodisomy", "Heterodisomy, Uniparental", "Uniparental Heterodisomies", "Heterodisomies, Uniparental"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uniparental Heterodisomy", "shortest_name_length": 24}
{"curie": "MONDO:0100033", "names": ["metabolic epilepsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metabolic epilepsy", "shortest_name_length": 18}
{"curie": "MONDO:0006146", "names": ["chondroid hamartoma", "Chondroid Hamartoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chondroid hamartoma", "shortest_name_length": 19}
{"curie": "MONDO:0009346", "names": ["histidinuria", "Histidinuria", "Hyperhistidinuria", "Renal histidinuria", "Histidine transport defect", "High urine histidine levels", "Elevated histidine in urine", "Histidinuria renal tubular defect", "Histidine transport defect (disorder)", "Histidinuria due to a Renal Tubular Defect", "histidinuria-renal tubular defect syndrome", "HISTIDINURIA DUE TO A RENAL TUBULAR DEFECT", "Histidinuria-renal tubular defect syndrome", "histidinuria due to a renal tubular defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "histidinuria due to a renal tubular defect", "shortest_name_length": 12}
{"curie": "UMLS:C0233796", "names": ["Amnesia transient", "temporary amnesia", "Temporary amnesia", "transient amnesia", "Transient amnesia", "amnesia temporary", "Temporary Amnesia", "Temporary Amnesias", "Amnesia, temporary", "Transitory amnesia", "Amnesia, Temporary", "Amnesias, Temporary", "transient memory loss", "Memory loss transient", "Transient memory loss", "temporary memory loss", "Temporary memory loss", "Temporary loss of memory", "temporary loss of memory", "Loss (of);memory(temporary)", "Temporary loss of memory (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Temporary Amnesia", "shortest_name_length": 17}
{"curie": "MONDO:0019124", "names": ["MPA", "Micropolyangiitis", "Microscopic Polyangiitis", "Microscopic polyangiitis", "microscopic polyangiitis", "Microscopic Polyarteritis", "Microscopic polyarteritis", "Polyangiitis, Microscopic", "microscopic polyarteritis", "Microscopic Polyangiitides", "Polyangiitides, Microscopic", "MPA - microscopic polyangiitis", "Microscopic polyarteritis nodosa", "microscopic polyarteritis nodosa", "polyarteritis nodosa microscopic", "Microscopic polyangiitis (disorder)", "microscopic polyarteritis nodosa (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microscopic polyangiitis", "shortest_name_length": 3}
{"curie": "MONDO:0011729", "names": ["STRK1", "Strk1", "stroke, susceptibility to, 1", "STROKE, SUSCEPTIBILITY TO, 1", "stroke, susceptibility to, type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stroke, susceptibility to, 1", "shortest_name_length": 5}
{"curie": "UMLS:C4316791", "names": ["Entamoeba histolytica Infection", "Entamoeba histolytica infection", "Entamoeba histolytica Infections", "Infection, Entamoeba histolytica", "Infections, Entamoeba histolytica", "infection due to Entamoeba histolytica", "Infection due to Entamoeba histolytica", "Infection caused by Entamoeba histolytica", "Infection due to Entamoeba histolytica, SAI", "Infection caused by Entamoeba histolytica (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Entamoeba histolytica Infection", "shortest_name_length": 31}
{"curie": "MONDO:0100084", "names": ["actinopathy", "ACTA1 disease", "actin myopathy", "alpha actinopathy", "alpha-actinopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alpha-actinopathy", "shortest_name_length": 11}
{"curie": "MONDO:0016654", "names": ["R5", "Ring 5", "rose cluster 5", "ROSE Cluster 5", "chromosome 5 ring", "ring chromosome 5", "Ring chromosome 5", "Ring chromosome type 5", "Ring chromosome 5 syndrome", "Ring chromosome 5 syndrome (disorder)", "Ring chromosome 5 syndrome (diagnosis)", "anomaly of chromosome pair ring chromosome 5 syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ring chromosome 5", "shortest_name_length": 2}
{"curie": "UMLS:C0852733", "names": ["Fatal Attempt", "Fatal Suicide", "Fatal Attempts", "Suicide, Fatal", "Fatal Suicides", "Completed Suicide", "Completed suicide", "Suicide, Completed", "Completed Suicides", "Accomplished suicide", "Suicide (accomplished)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Completed Suicide", "shortest_name_length": 13}
{"curie": "UMLS:C1701938", "names": ["APAH", "Associated Pulmonary Arterial Hypertension", "Associated pulmonary arterial hypertension", "Associated with pulmonary arterial hypertension", "Associated pulmonary arterial hypertension (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Associated Pulmonary Arterial Hypertension", "shortest_name_length": 4}
{"curie": "UMLS:C1334926", "names": ["EBV positive nasopharyngeal carcinoma", "Nasopharyngeal Nonkeratinizing Carcinoma", "Nasopharyngeal Non-Keratinizing Carcinoma", "Nasopharyngeal Throat Nonkeratinizing Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasopharyngeal Nonkeratinizing Carcinoma", "shortest_name_length": 37}
{"curie": "UMLS:C1333814", "names": ["Gestational Trophoblastic Tumor by FIGO Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gestational Trophoblastic Tumor by FIGO Stage", "shortest_name_length": 45}
{"curie": "MONDO:0025425", "names": ["ICH", "hepatitis contagiosa canis", "Hepatitis contagiosa canis", "canine infectious Hepatitis", "Infectious canine hepatitis", "Canine Infectious Hepatitis", "infectious canine hepatitis", "Canine adenovirus infection", "infectious canine Hepatitis", "Infectious Canine Hepatitis", "Hepatitis, canine infectious", "Hepatitis, Infectious Canine", "infectious Hepatitis, canine", "Infectious Hepatitis, Canine", "Canine Hepatitis, Infectious", "Hepatitis, Canine Infectious", "hepatitis, infectious canine", "canine Hepatitis, infectious", "canine infectious Hepatitides", "Canine Infectious Hepatitides", "infectious canine Hepatitides", "Infectious Canine Hepatitides", "Canine Hepatitides, Infectious", "Hepatitides, Infectious Canine", "Infectious Hepatitides, Canine", "infectious Hepatitides, canine", "Hepatitides, Canine Infectious", "canine Hepatitides, infectious", "Hepatitides, infectious canine", "Hepatitides, canine infectious", "Infectious canine hepatitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatitis, infectious canine", "shortest_name_length": 3}
{"curie": "MONDO:0018705", "names": ["ANOAC", "axonal neuropathy-optic atrophy-cognitive deficit syndrome", "infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0006671", "names": ["Bacteroides Infection", "Bacteroides infection", "Bacteroides Infections", "infection, Bacteroides", "Infection, Bacteroides", "infection; Bacteroides", "Bacteroides; infection", "infections, Bacteroides", "Infections, Bacteroides", "infection due to Bacteroides", "Infection due to Bacteroides", "Bacteroides infectious disease", "infection caused by Bacteroides", "Bacteroides disease or disorder", "Infection caused by Bacteroides", "Bacterial infection with bacteroides", "Bacteroides caused disease or disorder", "Infection caused by Bacteroides (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bacteroides infectious disease", "shortest_name_length": 21}
{"curie": "UMLS:C0751847", "names": ["Middle Cerebral Artery Embolic Infarction", "Embolic Infarction, Middle Cerebral Artery"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Embolic Infarction, Middle Cerebral Artery", "shortest_name_length": 41}
{"curie": "MONDO:0016742", "names": ["CNS mixed germ cell tumor", "CNS Mixed Germ Cell Tumor", "Mixed germ cell tumor of CNS", "Mixed Germ Cell Tumor of CNS", "mixed germ cell tumor of CNS", "mixed germ cell tumor of the CNS", "Mixed Germ Cell Tumor of the CNS", "central nervous system mixed germ cell tumor", "Central Nervous System Mixed Germ Cell Tumor", "Mixed germ cell tumor of central nervous system", "mixed germ cell tumor of central nervous system", "Mixed germ cell neoplasm of central nervous system", "mixed germ cell tumor of the central nervous system", "Mixed Germ Cell Tumor of the Central Nervous System", "mixed germ cell neoplasm of the central nervous system", "Mixed Germ Cell Neoplasm of the Central Nervous System", "Mixed germ cell neoplasm of central nervous system (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed germ cell tumor of central nervous system", "shortest_name_length": 25}
{"curie": "MONDO:0032760", "names": ["DEDDFA", "DEVELOPMENTAL DELAY WITH OR WITHOUT DYSMORPHIC FACIES AND AUTISM", "developmental delay with or without dysmorphic facies and autism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental delay with or without dysmorphic facies and autism", "shortest_name_length": 6}
{"curie": "UMLS:C1260886", "names": ["Lymphoid granulomatosis of lung", "Lung Lymphomatoid Granulomatosis", "Lymphomatoid granulomatosis of lung", "Lymphoid granulomatosis of the lung", "Pulmonary Lymphomatoid Granulomatosis", "Lymphomatoid granulomatosis of the lung", "LG - Lymphomatoid granulomatosis of lung", "Lymphomatoid granulomatosis of lung (disorder)", "Lymphomatoid granulomatosis of lung (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphomatoid granulomatosis of lung", "shortest_name_length": 31}
{"curie": "UMLS:C1881279", "names": ["ISORHYTHMIC DISSOCIATION", "Isorhythmic dissociation", "isorhythmic atrioventricular dissociation", "Isorhythmic Atrioventricular Dissociation", "isorhythmic atrioventricular dissociation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Isorhythmic Atrioventricular Dissociation", "shortest_name_length": 24}
{"curie": "UMLS:C1332184", "names": ["Atypical Meningioma", "Adult Atypical Meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Atypical Meningioma", "shortest_name_length": 19}
{"curie": "UMLS:C5441655", "names": ["breast metastasis", "metastasis breast", "Breast Metastases", "Breast metastases", "metastases breast", "Breast Metastasis", "breast metastases", "Metastasis to breast", "Metastases to breast", "Metastatic Tumor to the Breast", "Metastatic Cancer to the Breast", "Metastatic Neoplasm to the Breast", "Secondary malignant deposit to breast", "Secondary malignant neoplasm of breast", "secondary malignant neoplasm of breast", "Metastatic malignant neoplasm to breast", "Metastatic malignant neoplasm of breast", "Metastatic Malignant Neoplasm to the Breast", "Metastatic Malignant Neoplasm in the Breast", "secondary malignant neoplasm of breast (diagnosis)", "Metastatic malignant neoplasm to breast (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary malignant neoplasm of breast", "shortest_name_length": 17}
{"curie": "UMLS:C1411886", "names": ["disturbance; temperature regulation", "Disturbance of Temperature Regulation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disturbance of Temperature Regulation", "shortest_name_length": 35}
{"curie": "MONDO:0018320", "names": ["primary microcephaly-mild intellectual disability-young-onset diabetes syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary microcephaly-mild intellectual disability-young-onset diabetes syndrome", "shortest_name_length": 79}
{"curie": "UMLS:C1368107", "names": ["Aplastic marrow", "Bone Marrow Aplasia", "Aplasia bone marrow", "bone marrow aplasia", "APLASIA BONE MARROW", "Bone marrow aplasia", "bone marrow; aplasia", "Aplastic bone marrow", "aplasia; bone marrow", "Bone marrow aplastic", "bone marrow aplasia (diagnosis)", "Aplastic bone marrow (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aplastic bone marrow", "shortest_name_length": 15}
{"curie": "UMLS:C1336759", "names": ["Tobacco Chewing-Related Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tobacco Chewing-Related Carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0010418", "names": ["SPG34", "X-linked spastic paraplegia 34", "Spastic Paraplegia 34, X-Linked", "spastic paraplegia 34, X-linked", "SPASTIC PARAPLEGIA 34, X-LINKED", "hereditary spastic paraplegia 34", "X-linked spastic paraplegia type 34", "hereditary spastic paraplegia type 34", "SPASTIC PARAPLEGIA 34, X-LINKED (disorder)", "X-linked spastic paraplegia type 34 (disorder)", "spastic paraplegia 34, X-linked, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 34", "shortest_name_length": 5}
{"curie": "MONDO:0015137", "names": ["periodic fever", "Periodic fever", "Periodic fevers", "fever; periodic", "fevers periodic", "periodic; fever", "Fever, periodic", "Periodic fever syndrome", "Periodic Fever Syndrome", "periodic fever syndrome", "Periodic fever syndromes", "periodic fever syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "periodic fever syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0000908", "names": ["ARVC13", "ARVD13", "arrhythmogenic right ventricular dysplasia 13", "ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 13", "arrhythmogenic right ventricular dysplasia type 13", "arrhythmogenic right ventricular cardiomyopathy 13", "familial arrhythmogenic right ventricular dysplasia 13", "CTNNA3 arrhythmogenic right ventricular cardiomyopathy", "Familial Arrhythmogenic Right Ventricular Dysplasia 13", "ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 13", "arrhythmogenic right ventricular dysplasia, familial, 13", "arrhythmogenic right ventricular dysplasia, familial, type 13", "arrhythmogenic right ventricular cardiomyopathy caused by mutation in CTNNA3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arrhythmogenic right ventricular dysplasia 13", "shortest_name_length": 6}
{"curie": "MONDO:0009139", "names": ["Ddrd", "DDRD", "Rolland-Debuqois syndrome", "Rolland-Debuqois syndrome (disorder)", "dyssegmental dwarfism Rolland-Desbuquois type", "dyssegmental dysplasia Rolland-Desbuquois type", "Dyssegmental dwarfism, Rolland-Desbuquois type", "dyssegmental dwarfism, Rolland-Desbuquois type", "DYSSEGMENTAL DWARFISM, ROLLAND-DESBUQUOIS TYPE", "Dyssegmental dysplasia, Rolland-Desbuquois type", "dyssegmental dysplasia, Rolland-Desbuquois type", "DYSSEGMENTAL DYSPLASIA, ROLLAND-DESBUQUOIS TYPE", "Dyssegmental dysplasia - Rolland-Desbuquois type", "Anisospondylic camptomicromelic dwarfism Rolland-Desbuquois type", "ANISOSPONDYLIC CAMPTOMICROMELIC DWARFISM, ROLLAND-DESBUQUOIS TYPE", "Anisospondylic Camptomicromelic dwarfism, Rolland-Desbuquois type", "Anisospondylic camptomicromelic dwarfism, Rolland-Desbuquois type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyssegmental dysplasia, Rolland-Desbuquois type", "shortest_name_length": 4}
{"curie": "MONDO:0002123", "names": ["CALCINOSIS", "Calcinoses", "Calcinosis", "calcinoses", "calcinosis", "calcification", "Calcification", "Calcifications", "calcium deposit(s)", "macrocalcification", "deposit(s), calcium", "tissue calcification", "Calcinosis (disorder)", "calcifications tissue", "pathologic calcification", "Pathologic Calcification", "Tissue calcification NOS", "heterotopic calcification", "Calcification, Pathologic", "Extraskeletal calcification", "Calcium Deposits/Calcification", "Pathologically calcified structure", "pathologically calcified structure", "Calcium buildup in soft tissues of body"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "calcinosis", "shortest_name_length": 10}
{"curie": "MONDO:0020493", "names": ["Haddad syndrome", "ondine-Hirschsprung disease", "ondine-Hirschsprung syndrome", "congenital central alveolar hypoventilation-Hirschsprung disease syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Haddad syndrome", "shortest_name_length": 15}
{"curie": "UMLS:C1336170", "names": ["Stage IIA Ovarian Germ Cell Tumor", "stage IIA ovarian germ cell tumor", "Stage IIA Ovarian Germ Cell Tumor AJCC v7", "Stage IIA Ovarian Germ Cell Tumor AJCC v6", "Stage IIA Ovarian Germ Cell Tumor AJCC v6 and v7", "FIGO Stage IIA Malignant Ovarian Germ Cell Tumor", "FIGO Stage IIA Malignant Germ Cell Tumor of Ovary", "FIGO Stage IIA Malignant Ovarian Germ Cell Neoplasm", "FIGO Stage IIA Malignant Germ Cell Neoplasm of Ovary", "FIGO Stage IIA Malignant Germ Cell Tumor of the Ovary", "FIGO Stage IIA Malignant Germ Cell Neoplasm of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Ovarian Germ Cell Tumor AJCC v6 and v7", "shortest_name_length": 33}
{"curie": "MONDO:0000245", "names": ["Tokelu", "tokelau", "Tokelau", "Malabar itch", "Malabar; itch", "tokelau tinea", "itch; Malabar", "Tinea Tokelau", "tinea imbricata", "Tinea imbricata", "tinea; imbricata", "imbricata; tinea", "Tokelau; ringworm", "ringworm; Tokelau", "Tinea imbricata (disorder)", "tinea imbricata (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tinea imbricata", "shortest_name_length": 6}
{"curie": "MONDO:0032767", "names": ["PGL6", "paragangliomas 6", "PARAGANGLIOMAS 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paragangliomas 6", "shortest_name_length": 4}
{"curie": "UMLS:C5447335", "names": ["CDH1-Associated Breast Cancer Syndrome", "CDH1-Associated Breast Carcinoma Syndrome", "Hereditary Lobular Breast Cancer Syndrome", "Hereditary Lobular Breast Carcinoma Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CDH1-Associated Breast Carcinoma Syndrome", "shortest_name_length": 38}
{"curie": "UMLS:C1880537", "names": ["Epithelial Neoplasm (Antiquated)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epithelial Neoplasm (Antiquated)", "shortest_name_length": 32}
{"curie": "MONDO:0032800", "names": ["RRS2", "ROBINOW SYNDROME, AUTOSOMAL RECESSIVE 2", "robinow syndrome, autosomal recessive 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "robinow syndrome, autosomal recessive 2", "shortest_name_length": 4}
{"curie": "MONDO:0023368", "names": ["Ho Kaufman McAlister syndrome", "Ho-Kaufman-McAlister syndrome", "Ho Kaufman Mcalister syndrome", "cleft palate, micrognathia, Wormian bones, congenital heart disease, dislocated hips, absent tibiae, bowed fibulae, preaxial polydactyly of the feet"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ho-Kaufman-McAlister syndrome", "shortest_name_length": 29}
{"curie": "UMLS:C4521627", "names": ["Stage IVA Sinonasal Cancer AJCC v8", "Stage IVA Sinonasal Carcinoma AJCC v8", "Stage IVA Nasal Cavity and Paranasal Sinus Cancer", "Stage IVA Nasal Cavity and Paranasal Sinus Cancer AJCC v8", "Stage IVA Nasal Cavity and Paranasal Sinus Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Nasal Cavity and Paranasal Sinus Cancer AJCC v8", "shortest_name_length": 34}
{"curie": "UMLS:C5204121", "names": ["PGNMID", "Proliferative Glomerulonephritis with Monoclonal IgG Deposits"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Proliferative Glomerulonephritis with Monoclonal IgG Deposits", "shortest_name_length": 6}
{"curie": "MONDO:0034989", "names": ["intellectual disability-cardiac anomalies-short stature-joint laxity syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability-cardiac anomalies-short stature-joint laxity syndrome", "shortest_name_length": 77}
{"curie": "UMLS:C2837942", "names": ["Malignant Inner Ear Neoplasm", "Malignant neoplasm of inner ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Inner Ear Neoplasm", "shortest_name_length": 28}
{"curie": "UMLS:C4725678", "names": ["BSSRCC", "Bilateral Synchronous Sporadic Renal Cell Cancer", "Bilateral Synchronous Sporadic Renal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bilateral Synchronous Sporadic Renal Cell Carcinoma", "shortest_name_length": 6}
{"curie": "MONDO:0008977", "names": ["chondrosarcoma", "Chondrosarcoma", "CHONDROSARCOMA", "chondrosarcomas", "Chondrosarcomas", "Chondrosarcoma NOS", "Fibrochondrosarcoma", "Chondrosarcoma, NOS", "Cartilaginous cancer", "Primary Chondrosarcoma", "chondrosarcoma of bone", "Chondroma sarcomatosum", "chondrosarcoma (disease)", "Chondrosarcoma (disorder)", "Chondrosarcoma morphology", "chondrosarcoma, malignant", "CHONDROSARCOMA, MALIGNANT", "chondrosarcoma (diagnosis)", "Primary Bone Chondrosarcoma", "Primary Central Chondrosarcoma", "OSTEOCHONDROSARCOMA, MALIGNANT", "Primary Chondrosarcoma of Bone", "Primary chondrosarcoma of bone", "chondrosarcoma, somatic mutation", "malignant neoplasm chondrosarcoma", "chondrosarcoma; (site unspecified)", "Primary Chondrosarcoma of the Bone", "primary chondrosarcoma of the bone", "Chondrosarcoma (morphologic abnormality)", "Primary chondrosarcoma of bone (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chondrosarcoma", "shortest_name_length": 14}
{"curie": "UMLS:C1333004", "names": ["Pediatric Supratentorial Tumor", "Childhood Supratentorial Tumor", "Childhood Supratentorial Tumors", "Childhood Supratentorial Neoplasm", "Pediatric Supratentorial Neoplasm", "Childhood Supratentorial Neoplasms"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Supratentorial Neoplasm", "shortest_name_length": 30}
{"curie": "MONDO:0030870", "names": ["POF17", "premature ovarian failure 17", "PREMATURE OVARIAN FAILURE 17", "primary ovarian insufficiency 17"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "premature ovarian failure 17", "shortest_name_length": 5}
{"curie": "MONDO:0024568", "names": ["ILFS1", "LARS infantile liver failure", "Lars infantile liver failure", "infantile liver failure syndrome 1", "INFANTILE LIVER FAILURE SYNDROME 1", "infantile liver failure syndrome type 1", "infantile liver failure caused by mutation in LARS", "infantile liver failure caused by mutation in Lars", "acute infantile liver failure - multisystemic involvement syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile liver failure syndrome 1", "shortest_name_length": 5}
{"curie": "MONDO:0054837", "names": ["MRD57", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 57", "mental retardation, autosomal dominant 57", "intellectual disability, autosomal dominant 57", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 57", "intellectual developmental disorder, autosomal dominant 57"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 57", "shortest_name_length": 5}
{"curie": "UMLS:C4682573", "names": ["Stage IIIB Uterine Corpus Endometrial Stromal Sarcoma", "Stage IIIB Uterine Corpus Endometrial Stromal Sarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Uterine Corpus Endometrial Stromal Sarcoma AJCC v8", "shortest_name_length": 53}
{"curie": "MONDO:0019333", "names": ["autosomal recessive hyperinsulinism due to SUR1 deficiency", "autosomal recessive hyperinsulinemic hypoglycemia due to SUR1 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive hyperinsulinism due to SUR1 deficiency", "shortest_name_length": 58}
{"curie": "MONDO:0018964", "names": ["Methylcobalamin deficiency", "methylcobalamin deficiency", "Functional methionine synthase deficiency", "functional methionine synthase deficiency", "Methylmalonic acidemia without homocystinuria", "homocystinuria without methylmalonic aciduria", "Homocystinuria without methylmalonic aciduria", "Methylmalonic aciduria without homocystinuria", "Homocystinuria without methylmalonic aciduria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "homocystinuria without methylmalonic aciduria", "shortest_name_length": 26}
{"curie": "UMLS:C3898662", "names": ["Premature Menarche", "Isolated Premature Menarche"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Isolated Premature Menarche", "shortest_name_length": 18}
{"curie": "MONDO:0003956", "names": ["Baastrup", "kissing spine", "Kissing spine", "kissing spines", "Baastrup syndrome", "baastrup's syndrome", "Baastrup's syndrome", "Kissing spine syndrome", "Kissing spine (disorder)", "Osteoarthrosis interspinalis", "Kissing spine, site unspecified", "Baastrup's syndrome (diagnosis)", "Overriding dorsal spinous processes", "Overriding of dorsal spinous processes", "Localised idiopathic skeletal hyperostosis", "Localized idiopathic skeletal hyperostosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Baastrup syndrome", "shortest_name_length": 8}
{"curie": "MONDO:0009501", "names": ["ERYTHROCYTE LACTATE TRANSPORTER DEFECT", "Erythrocyte Lactate Transporter Defect", "erythrocyte lactate transporter defect", "Erythrocyte lactate transporter defect", "lactate transporter defect, myopathy due to", "Lactate Transporter Defect, Myopathy due to", "LACTATE TRANSPORTER DEFECT, MYOPATHY DUE TO", "metabolic myopathy due to lactate transporter defect", "Metabolic myopathy due to lactate transporter defect", "Metabolic myopathy due to lactate transporter defect (disorder)", "Metabolic myopathy due to lactate transporter defect (diagnosis)", "myopathies in metabolic diseases due to lactate transporter defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metabolic myopathy due to lactate transporter defect", "shortest_name_length": 38}
{"curie": "UMLS:C0346086", "names": ["Skin Angioendothelioma", "Skin Hemangioendothelioma", "Angioendothelioma of Skin", "Hemangioendothelioma of Skin", "Hemangioendothelioma of skin", "Haemangioendothelioma of skin", "Angioendothelioma of the Skin", "Hemangioendothelioma of the Skin", "Hemangioendothelioma of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemangioendothelioma of skin", "shortest_name_length": 22}
{"curie": "UMLS:C4329281", "names": ["Advanced Solid Tumor", "Advanced Solid Neoplasm", "Advanced Malignant Solid Tumor", "Advanced Malignant Solid Neoplasm", "Advanced Non-Hematologic Malignancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Malignant Solid Neoplasm", "shortest_name_length": 20}
{"curie": "MONDO:0015774", "names": ["Thoraco-abdominal enteric duplication", "thoraco abdominal enteric duplication", "thoraco-abdominal enteric duplication", "Thoraco-abdominal enteric duplication (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thoraco-abdominal enteric duplication", "shortest_name_length": 37}
{"curie": "UMLS:C0149797", "names": ["umbilical granuloma", "UMBILICAL GRANULOMA", "Umbilical granuloma", "Granuloma;umbilicus", "Umbilical Granuloma", "granulomas umbilical", "granuloma; umbilicus", "umbilicus; granuloma", "granuloma of umbilical cord", "Umbilical granuloma (disorder)", "granuloma of umbilical cord (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Umbilical granuloma", "shortest_name_length": 19}
{"curie": "MONDO:0017009", "names": ["partial trisomy of chromosome Xp", "partial duplication of chromosome Xp", "partial trisomy of the short arm of chromosome X", "partial duplication of the short arm of chromosome X", "partial duplication of the short arm of chromosome type X"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of the short arm of chromosome X", "shortest_name_length": 32}
{"curie": "UMLS:C4331334", "names": ["Stage IV Nasopharyngeal Throat Cancer", "Stage IV Nasopharyngeal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Nasopharyngeal Carcinoma AJCC v8", "shortest_name_length": 37}
{"curie": "UMLS:C4289325", "names": ["FIGO Stage IC1 Ovarian Cancer", "FIGO Stage IC1 Ovarian Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Stage IC1 Ovarian Cancer", "shortest_name_length": 29}
{"curie": "UMLS:C5421316", "names": ["Recurrent Esophageal Anastomotic Stricture"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Esophageal Anastomotic Stricture", "shortest_name_length": 42}
{"curie": "MONDO:0014075", "names": ["CTRCT39", "cataract 39 multiple types", "CATARACT 39, MULTIPLE TYPES", "cataract 39, multiple types", "CRYGB early-onset non-syndromic cataract", "autosomal dominant cataract 39 multiple types", "cataract 39, multiple types, autosomal dominant", "early-onset non-syndromic cataract caused by mutation in CRYGB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 39 multiple types", "shortest_name_length": 7}
{"curie": "MONDO:0016454", "names": ["AR-CMT2B5", "SEOAN due to NEFL deficiency", "Charcot-Marie-Tooth disease type 2B5", "autosomal recessive Charcot-Marie-Tooth disease type 2B5", "severe early-onset axonal neuropathy due to NEFL deficiency", "severe early-onset axonal neuropathy due to light neurofilament subunit deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 2B5", "shortest_name_length": 9}
{"curie": "UMLS:C4725859", "names": ["Refractory Dedifferentiated Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Dedifferentiated Liposarcoma", "shortest_name_length": 39}
{"curie": "MONDO:0004656", "names": ["RUBELLA", "rubella", "Rubella", "Rubellas", "Rubella NOS", "Rubella, NOS", "german measle", "third disease", "THIRD DISEASE", "GERMAN MEASLES", "German measles", "German Measles", "german measles", "Measles, German", "Three Day Measle", "Three-Day Measles", "Rubella infection", "three-day measles", "Three Day Measles", "three-Day Measles", "Three day measles", "three day measles", "Rubella Infection", "Measle, Three Day", "Measles, Three Day", "Rubella (disorder)", "rubella (diagnosis)", "german measles rubella", "Rubella [German measles]", "rubella (German measles)", "Rubella virus infectious disease", "Rubella virus disease or disorder", "Rubella without mention of complication", "Rubella virus caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rubella", "shortest_name_length": 7}
{"curie": "UMLS:C1332851", "names": ["Heart Paraganglioma", "Cardiac Paraganglioma", "Paraganglioma of Heart", "Paraganglioma of the Heart"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiac Paraganglioma", "shortest_name_length": 19}
{"curie": "MONDO:0016747", "names": ["CNS melanoma", "CNS Melanoma", "melanoma of CNS", "Melanoma of CNS", "melanoma of the CNS", "Melanoma of the CNS", "primary CNS melanoma", "primary meningeal melanoma", "primary melanoma of the CNS", "Primary melanoma of the CNS", "malignant melanoma of meninges", "Malignant melanoma of meninges", "Central nervous system melanoma", "Central Nervous System Melanoma", "central nervous system melanoma", "melanoma of central nervous system", "Melanoma of Central Nervous System", "Melanoma of the Central Nervous System", "melanoma of the Central nervous system", "Primary Central Nervous System Melanoma", "central nervous system melanoma (disease)", "Malignant melanoma of meninges (disorder)", "melanoma (disease) of central nervous system", "Primary melanoma of the central nervous system", "primary melanoma of the central nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary melanoma of the central nervous system", "shortest_name_length": 12}
{"curie": "MONDO:0018164", "names": ["ATOS", "Arterial TOS", "arterial TOS", "arterial cervical rib syndrome", "Arterial cervical rib syndrome", "arterial hyperabduction syndrome", "Arterial hyperabduction syndrome", "arterial costoclavicular syndrome", "arterial thoracic outlet syndrome", "Arterial thoracic outlet syndrome", "Arterial costoclavicular syndrome", "Arterial Thoracic Outlet Syndrome", "arterial scalenus anticus syndrome", "Arterial scalenus anticus syndrome", "Arterial thoracic outlet syndrome (disorder)", "arterial thoracic outlet compression syndrome", "Arterial thoracic outlet compression syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arterial thoracic outlet syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C1336432", "names": ["Stage IV Ovarian Polyembryoma", "Ovarian Polyembryoma Stage IV", "Stage IV Ovarian Polyembryoma AJCC v7", "Stage IV Ovarian Polyembryoma AJCC v6", "Stage IV Ovarian Polyembryoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Ovarian Polyembryoma AJCC v6 and v7", "shortest_name_length": 29}
{"curie": "UMLS:C0279068", "names": ["Solid Tumor", "pediatric solid tumor", "Childhood Solid Tumor", "childhood solid tumor", "Pediatric Solid Tumor", "solid tumor, childhood", "Childhood Solid Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Solid Neoplasm", "shortest_name_length": 11}
{"curie": "UMLS:C0853856", "names": ["Staphylococcal abscess"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Staphylococcal abscess", "shortest_name_length": 22}
{"curie": "UMLS:C0948691", "names": ["Cerebral aspergillosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebral aspergillosis", "shortest_name_length": 22}
{"curie": "MONDO:0009900", "names": ["BONNEAU SYNDROME", "Bonneau Syndrome", "Bonneau syndrome", "polysyndactyly cardiac malformation", "Polysyndactyly with Cardiac Malformation", "POLYSYNDACTYLY WITH CARDIAC MALFORMATION", "polysyndactyly with CARDIAC malformation", "Polysyndactyly-cardiac malformation syndrome", "polysyndactyly-cardiac malformation syndrome", "Polysyndactyly and cardiac malformation syndrome", "Polysyndactyly and cardiac malformation syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polysyndactyly-cardiac malformation syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0004128", "names": ["Occult Large Cell Lung Carcinoma", "lung occult large cell carcinoma", "occult large cell lung carcinoma", "Occult Lung Large Cell Carcinoma", "occult large cell carcinoma of lung", "Occult Large Cell Carcinoma of Lung", "Occult large cell carcinoma of the lung", "Occult Large Cell Carcinoma of the Lung", "occult large cell carcinoma of the lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung occult large cell carcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C1334856", "names": ["Myxoid Rhabdomyoma", "Classic Rhabdomyoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Classic Rhabdomyoma", "shortest_name_length": 18}
{"curie": "UMLS:C0340773", "names": ["Vein rupture", "vein rupture", "ruptures vein", "rupture of vein", "Rupture of vein", "Rupture of vein (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rupture of vein", "shortest_name_length": 12}
{"curie": "MONDO:0017934", "names": ["aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome", "aphonia-deafness-retinal dystrophy-duplicated halluces-intellectual disability syndrome", "aphonia-hearing loss-retinal dystrophy-duplicated halluces-intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome", "shortest_name_length": 82}
{"curie": "UMLS:C0751498", "names": ["sigmoid colon carcinoma", "Sigmoid Colon Carcinoma", "Carcinoma of sigmoid colon", "carcinoma of sigmoid colon", "Carcinoma of sigmoid colon (disorder)", "Carcinoma of sigmoid colon (diagnosis)", "malignant large intestine neoplasm carcinoma of sigmoid colon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carcinoma of sigmoid colon", "shortest_name_length": 23}
{"curie": "MONDO:0014352", "names": ["AOMS3", "DYRK1B metabolic syndrome", "abdominal obesity-metabolic syndrome 3", "ABDOMINAL OBESITY-METABOLIC SYNDROME 3", "abdominal obesity-metabolic syndrome type 3", "metabolic syndrome caused by mutation in DYRK1B", "central obesity, type 2 diabetes, hypertension, and early-onset coronary artery disease", "CENTRAL OBESITY, TYPE 2 DIABETES, HYPERTENSION, AND EARLY-ONSET CORONARY ARTERY DISEASE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "abdominal obesity-metabolic syndrome 3", "shortest_name_length": 5}
{"curie": "UMLS:C5205938", "names": ["Prostate Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Melanoma", "shortest_name_length": 17}
{"curie": "MONDO:0018018", "names": ["SSA", "ATTRwt amyloidosis", "Old age amyloidosis", "wild-type amyloidosis", "Age related amyloidosis", "wild type ATTR amyloidosis", "ATTR amyloidosis wild type", "Wild type ATTR amyloidosis", "wild-type ATTR amyloidosis", "ATTRwt-related amyloidosis", "Senile systemic amyloidosis", "senile systemic amyloidosis", "wild type ATTR-related amyloidosis", "Wild type ATTR-related amyloidosis", "Wild type ATTR amyloidosis (disorder)", "wild-type transthyretin cardiac amyloidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "wild type ATTR amyloidosis", "shortest_name_length": 3}
{"curie": "UMLS:C1883403", "names": ["Sweat Gland Tubular Carcinoma", "Sweat Gland Tubular Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sweat Gland Tubular Carcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0017819", "names": ["atypical dentin dysplasia due to SMOC2 deficiency", "dentin dysplasia type 1 with microdontia and shape anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical dentin dysplasia due to SMOC2 deficiency", "shortest_name_length": 49}
{"curie": "MONDO:0000332", "names": ["sennetsu fever", "Sennetsu Fever", "Sennetsu fever", "sennetsu ehrlichiosis", "Sennetsu ehrlichiosis", "Sennetsu fever (disorder)", "Human Ehrlichial infection, sennetsu type", "Human Ehrlichial infection, Sennetsu type", "Neorickettsia sennetsu infectious disease", "Neorickettsia sennetsu disease or disorder", "Neorickettsia sennetsu caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sennetsu fever", "shortest_name_length": 14}
{"curie": "MONDO:0002717", "names": ["Intramedullary Spinal Teratoma", "Intramedullary Spinal teratoma", "intramedullary spinal teratoma", "spinal cord intramedullary teratoma", "intramedullary spinal cord teratoma", "Intramedullary Spinal Cord Teratoma", "intramedullary teratoma of spinal cord", "Intramedullary Teratoma of Spinal Cord", "intramedullary teratoma of the spinal cord", "Intramedullary Teratoma of the Spinal Cord"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal cord intramedullary teratoma", "shortest_name_length": 30}
{"curie": "UMLS:C4277690", "names": ["Ciliopathy", "Ciliopathies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ciliopathies", "shortest_name_length": 10}
{"curie": "MONDO:0014185", "names": ["Del(3)(q13)", "Monosomy 3q13", "Deletion 3q13", "monosomy 3q13", "3q13 microdeletion syndrome", "Chromosome 3, monosomy 3q13", "chromosome 3q13.31 deletion syndrome", "CHROMOSOME 3q13.31 DELETION SYNDROME", "3q13 microdeletion syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 3q13.31 deletion syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0100261", "names": ["PEX3 related Zellweger spectrum disorder", "peroxisome biogenesis disorder due to PEX3 defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder due to PEX3 defect", "shortest_name_length": 40}
{"curie": "MONDO:0018935", "names": ["HCL", "HCL-C", "hairy cell leukemia", "Hairy-cell leukemia", "Hairy Cell Leukemia", "HAIRY CELL LEUKEMIA", "hairy-cell leukemia", "leukemia hairy cell", "Hairy cell leukemia", "cell hairy leukemia", "LEUKEMIA HAIRY CELL", "leukemia hairy-cell", "Leukemia, hairy cell", "leukemia; hairy cell", "leukemia, hairy cell", "hairy cell leukaemia", "Hairy-cell leukaemia", "Hairy Cell Leukemias", "cells hairy leukemia", "Hairy cell leukaemia", "hairy-cell leukaemia", "leukaemia hairy cell", "Leukemia, Hairy Cell", "Leukemia, Hairy cell", "HAIRY CELL LEUKAEMIA", "Leukemias, Hairy Cell", "Leukemia - hairy cell", "hairy T cell leukemia", "Hairy cell leukemia NOS", "HCL - Hairy cell leukemia", "HCL - Hairy cell leukaemia", "Classic hairy cell leukemia", "classic hairy cell leukemia", "Hairy cell leukemia (clinical)", "Leukemic reticuloendotheliosis", "Leukemic Reticuloendothelioses", "leukemic reticuloendotheliosis", "Hairy cell leukemia (disorder)", "Leukemic Reticuloendotheliosis", "RETICULOENDOTHELIOSIS, LEUKEMIC", "leukemic; reticuloendotheliosis", "reticuloendotheliosis; leukemic", "Leukaemic reticuloendotheliosis", "Reticuloendothelioses, Leukemic", "Hairy cell leukaemia (clinical)", "Reticuloendotheliosis, Leukemic", "hairy cell leukemia (diagnosis)", "LRE - Leukemic reticuloendotheliosis", "LRE - Leukaemic reticuloendotheliosis", "Hairy cell leukemia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hairy cell leukemia", "shortest_name_length": 3}
{"curie": "UMLS:C1710482", "names": ["Trichofollicular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Trichofollicular Carcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0014924", "names": ["FFEVF2", "epilepsy, familial focal, with variable foci 2", "EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 2", "NPRL2 epilepsy, familial focal, with variable foci", "epilepsy, familial focal, with variable foci type 2", "epilepsy, familial focal, with variable foci 2; FFEVF2", "epilepsy, familial focal, with variable foci caused by mutation in NPRL2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, familial focal, with variable foci 2", "shortest_name_length": 6}
{"curie": "UMLS:C1709781", "names": ["PAL", "Pyothorax-Associated Lymphoma", "Pleural Diffuse Large B-Cell Lymphoma Associated with Chronic Inflammation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pyothorax-Associated Lymphoma", "shortest_name_length": 3}
{"curie": "MONDO:0015065", "names": ["ileal neuroendocrine tumor", "Ileal Neuroendocrine Tumor", "ileal neuroendocrine neoplasm", "ileal neuroendocrine tumor, well differentiated, low or intermediate grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ileal neuroendocrine tumor, well differentiated, low or intermediate grade", "shortest_name_length": 26}
{"curie": "MONDO:0000136", "names": ["keratosis pilaris decalvans", "Keratosis pilaris decalvans", "Keratosis pilaris decalvans (disorder)", "keratosis follicularis spinulosa decalvans", "Keratosis follicularis spinulosa decalvans", "follicularis; keratosis, spinulosa (decalvans)", "keratosis; follicularis, spinulosa (decalvans)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratosis follicularis spinulosa decalvans", "shortest_name_length": 27}
{"curie": "MONDO:0008394", "names": ["SRS", "RSS", "Russell dwarf", "Russell-Silver", "Russell nanism", "silver syndrome", "Silver syndrome", "silvers syndrome", "Russell syndrome", "russell syndrome", "Silver's syndrome", "russell's syndrome", "Russell's syndrome", "Silver-Russell Dwarfism", "Silver-Russell syndrome", "Russell-Silver dwarfism", "Silver-Russell dwarfism", "Silver Russell syndrome", "Russell Silver syndrome", "Russell-Silver Dwarfism", "Silver Russell dwarfism", "Russell-Silver syndrome", "RUSSELL-SILVER SYNDROME", "Russell-Silver Syndrome", "russell silver syndrome", "SILVER-RUSSELL DWARFISM", "Silver-Russell Syndrome", "russell-silver syndrome", "silver russell syndrome", "Silver Russell Syndrome", "Russell Silver Syndrome", "Silver Russell Dwarfism", "silver-russell syndrome", "Dwarfism, Silver Russell", "russell silvers syndrome", "Syndrome, Silver-Russell", "Dwarfism, Silver-Russell", "Syndrome, Russell Silver", "Russell-Silver syndrome (RSS)", "Silver-Russell syndrome (SRS)", "Russell-Silver syndrome (disorder)", "Russell-Silver syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Silver-Russell syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0800090", "names": ["ectrodactyly with and without other manifestations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectrodactyly with and without other manifestations", "shortest_name_length": 50}
{"curie": "MONDO:0013434", "names": ["CILD14", "primary ciliary dyskinesia 14", "Primary Ciliary Dyskinesia 14", "ciliary dyskinesia, primary, 14", "CILIARY DYSKINESIA, PRIMARY, 14", "CCDC39 primary ciliary dyskinesia", "primary ciliary dyskinesia type 14", "ciliary dyskinesia, primary, type 14", "primary ciliary dyskinesia caused by mutation in CCDC39", "primary ciliary dyskinesia 14 with or without situs inversus", "CILIARY DYSKINESIA, PRIMARY, 14, WITH OR WITHOUT SITUS INVERSUS", "ciliary dyskinesia, primary, 14, with or without situs inversus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia 14", "shortest_name_length": 6}
{"curie": "MONDO:0040698", "names": ["Subacute bursitis", "subacute bursitis", "Subacute bursitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subacute bursitis", "shortest_name_length": 17}
{"curie": "UMLS:C4764083", "names": ["Refractory Transformed B-Cell Non-Hodgkin Lymphoma", "Refractory Transformed Indolent B-Cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Transformed B-Cell Non-Hodgkin Lymphoma", "shortest_name_length": 50}
{"curie": "UMLS:C1519916", "names": ["Vaginal Basaloid Carcinoma", "Vaginal Basaloid Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Basaloid Carcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0016297", "names": ["Isolated prelingual genetic deafness", "isolated prelingual genetic deafness", "Prelingual non-syndromic genetic deafness", "prelingual non-syndromic genetic deafness", "prelingual non-syndromic genetic hearing loss", "Prelingual non-syndromic genetic deafness (disorder)", "Prelingual non-syndromic genetic deafness (diagnosis)", "sensorineural hearing loss prelingual non-syndromic genetic deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prelingual non-syndromic genetic hearing loss", "shortest_name_length": 36}
{"curie": "MONDO:0004546", "names": ["Lumbar Plexus Tumor", "lumbar plexus tumor", "Tumor of Lumbar Plexus", "lumbar plexus neoplasm", "tumor of lumbar plexus", "Lumbar Plexus Neoplasm", "tumor of Lumbar Plexus", "Lumbar Plexus Neoplasms", "lumbar plexus neoplasms", "lumbar nerve plexus tumor", "neoplasm of lumbar plexus", "Neoplasm of Lumbar Plexus", "tumor of the lumbar plexus", "Tumor of the Lumbar Plexus", "tumor of lumbar nerve plexus", "lumbar nerve plexus neoplasm", "Neoplasm of the Lumbar Plexus", "neoplasm of the lumbar plexus", "neoplasm of lumbar nerve plexus", "lumbar nerve plexus neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lumbar plexus neoplasm", "shortest_name_length": 19}
{"curie": "MONDO:0011736", "names": ["CREE MENTAL RETARDATION SYNDROME", "Cree Mental Retardation Syndrome", "Cree mental retardation syndrome", "Cree intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cree intellectual disability syndrome", "shortest_name_length": 32}
{"curie": "MONDO:0011992", "names": ["SPG25", "spastic paraplegia 25", "hereditary spastic paraplegia 25", "hereditary spastic paraplegia type 25", "autosomal recessive spastic paraplegia 25", "Spastic paraplegia 25, autosomal recessive", "SPASTIC PARAPLEGIA 25, AUTOSOMAL RECESSIVE", "spastic paraplegia 25, autosomal recessive", "Autosomal recessive spastic paraplegia type 25", "autosomal recessive spastic paraplegia type 25", "familial spastic paraplegia autosomal recessive type 25", "Autosomal recessive spastic paraplegia type 25 (disorder)", "Autosomal recessive spastic paraplegia type 25 (diagnosis)", "Disc herniation with spastic paraplegia, autosomal recessive", "DISC HERNIATION WITH SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE", "Disc Herniation With Spastic Paraplegia, Autosomal Recessive", "Autosomal recessive spastic paraplegia disc herniation syndrome", "Autosomal recessive spastic paraplegia-disc herniation syndrome", "autosomal recessive spastic paraplegia-disc herniation syndrome", "Spinal disc herniation with autosomal recessive spastic paraplegia", "spinal disc herniation with autosomal recessive spastic paraplegia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 25", "shortest_name_length": 5}
{"curie": "UMLS:C1336723", "names": ["Testicular Non-Neoplastic Disease", "Testicular Non-Neoplastic Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular Non-Neoplastic Disorder", "shortest_name_length": 33}
{"curie": "UMLS:C0154933", "names": ["synechia", "Synechia", "synechiae", "Iris synechia", "Synechiae NOS", "iris; adhesion", "Iris synechiae", "iris adhesions", "Iris adhesions", "adhesion; iris", "iris syncechiae", "adhesion of iris", "adhesions of iris", "Synechiae of iris", "Adhesions of iris", "Synechia (iris) NOS", "Synechiae of iris NOS", "Adhesions of iris, NOS", "Synechiae of iris, NOS", "Adhesions of iris (disorder)", "adhesion of iris (diagnosis)", "Unspecified adhesions of iris", "Adhesions of iris, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adhesions of iris", "shortest_name_length": 8}
{"curie": "MONDO:0016428", "names": ["multiple sclerosis variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple sclerosis variant", "shortest_name_length": 26}
{"curie": "MONDO:0006898", "names": ["periarthritis", "Periarthritis", "Periarthritides", "Periarthritis NOS", "Periarthritis, NOS", "Calcific periarthritis", "Periarthritis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "periarthritis", "shortest_name_length": 13}
{"curie": "UMLS:C0935806", "names": ["Stage II Merkel Cell Cancer", "stage II Merkel cell carcinoma", "Stage II Merkel Cell Carcinoma", "Merkel cell carcinoma, stage II", "Stage II Merkel Cell Carcinoma AJCC v7", "stage II neuroendocrine carcinoma of the skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Merkel Cell Carcinoma AJCC v7", "shortest_name_length": 27}
{"curie": "MONDO:0016722", "names": ["Pineal PNET", "pineal PNET", "pineoblastoma", "Pineoblastoma", "Pineoblastomas", "Pinealblastoma", "pinealblastoma", "Pinealoblastoma", "pinealoblastoma", "Pineal Gland PNET", "pineal gland PNET", "PNET of Pineal Gland", "PNET of pineal gland", "Pineoblastoma (disorder)", "PNET of the Pineal Gland", "PINEOBLASTOMA, MALIGNANT", "pineoblastoma, malignant", "PNET of the pineal gland", "pineoblastoma (diagnosis)", "Pineoblastoma (WHO Grade 4)", "pineoblastoma (WHO grade IV)", "Pineoblastoma (WHO Grade IV)", "pineal primitive neuroectodermal tumor", "Pineal Primitive Neuroectodermal Tumor", "Pineoblastoma (morphologic abnormality)", "pineal primitive neuroectodermal neoplasm", "Pineal Primitive Neuroectodermal Neoplasm", "pineal gland primitive neuroectodermal tumor", "pineal body neoplasm malignant pineoblastoma", "Pineal Gland Primitive Neuroectodermal Tumor", "Primitive Neuroectodermal Tumor of Pineal Gland", "pineal gland primitive neuroectodermal neoplasm", "Pineal Gland Primitive Neuroectodermal Neoplasm", "primitive neuroectodermal tumor of pineal gland", "primitive neuroectodermal neoplasm of pineal gland", "Primitive Neuroectodermal Neoplasm of Pineal Gland", "primitive neuroectodermal tumor of the pineal gland", "Primitive Neuroectodermal Tumor of the Pineal Gland", "Primitive Neuroectodermal Neoplasm of the Pineal Gland", "primitive neuroectodermal neoplasm of the pineal gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pineoblastoma", "shortest_name_length": 11}
{"curie": "MONDO:0006368", "names": ["PMT", "Phosphaturic Mesenchymal Tumor", "Phosphaturic mesenchymal tumor", "phosphaturic mesenchymal tumor", "Phosphaturic Mesenchymal Tumor, Mixed Connective Tissue Type", "phosphaturic mesenchymal tumor, mixed connective tissue type", "Phosphaturic Mesenchymal Tumor, Mixed Connective Tissue Variant", "phosphaturic mesenchymal tumor, mixed connective tissue variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phosphaturic mesenchymal tumor", "shortest_name_length": 3}
{"curie": "MONDO:0700175", "names": ["feline neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "feline neoplasm", "shortest_name_length": 15}
{"curie": "MONDO:0012237", "names": ["NEM6", "NEMALINE MYOPATHY 6", "nemaline myopathy 6", "Nemaline myopathy 6", "nemaline myopathy type 6", "KBTBD13 nemaline myopathy", "nemaline myopathy 6, autosomal dominant", "nemaline myopathy caused by mutation in KBTBD13"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nemaline myopathy 6", "shortest_name_length": 4}
{"curie": "UMLS:C0854852", "names": ["Peripheral T-cell lymphoma unspecified refractory", "Refractory Unspecified Peripheral T-Cell Lymphoma", "Refractory Peripheral T-Cell Lymphoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peripheral T-cell lymphoma unspecified refractory", "shortest_name_length": 49}
{"curie": "UMLS:C5420172", "names": ["Nasopharyngeal Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasopharyngeal Hodgkin Lymphoma", "shortest_name_length": 31}
{"curie": "UMLS:C4053999", "names": ["Spindle Cell/Sclerosing Rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spindle Cell/Sclerosing Rhabdomyosarcoma", "shortest_name_length": 40}
{"curie": "UMLS:C1334402", "names": ["Lipomatous hemangiopericytoma", "Lipomatous Hemangiopericytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lipomatous hemangiopericytoma", "shortest_name_length": 29}
{"curie": "UMLS:C1519368", "names": ["Anaplastic Large Cell Lymphoma, Giant Cell Rich Subtype"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anaplastic Large Cell Lymphoma, Giant Cell Rich Subtype", "shortest_name_length": 55}
{"curie": "MONDO:0008362", "names": ["RAGWEED SENSITIVITY", "ragweed sensitivity", "Ragweed Sensitivity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ragweed sensitivity", "shortest_name_length": 19}
{"curie": "MONDO:0017042", "names": ["Td", "TD", "thanatophoric dwarf", "Thanatophoric dwarf", "Dwarf, thanatophoric", "dwarfism thanatophoric", "Thanatophoric dwarfism", "thanatophoric dwarfism", "Thanatophoric Dwarfism", "thanatophoric dysplasia", "dwarfism; thanatophoric", "Thanatophoric Dwarfisms", "Dwarfism, Thanatophoric", "Thanatophoric dysplasia", "Thanatophoric Dysplasia", "thanatophoric; dwarfism", "Thanatophoric Dysplasias", "Dwarfisms, Thanatophoric", "Dysplasia, Thanatophoric", "Dysplasias, Thanatophoric", "Thanatophoric short stature", "Thanatophoric Short Stature", "thanatophoric short stature", "TD - Thanatophoric dwarfism", "thanatophoric dysplasia (TD)", "stature; short, thanatophoric", "short; stature, thanatophoric", "Thanatophoric dwarfism syndrome", "Thanatophoric dysplasia (disorder)", "thanatophoric short stature (diagnosis)", "thanatophoric dwarfism or short stature", "osteochondrodysplasia with defects of growth of tubular bones and spine thanatophoric short stature"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thanatophoric dysplasia", "shortest_name_length": 2}
{"curie": "MONDO:0019917", "names": ["MBCS", "UPD(20)mat", "Maternal UPD(20)", "maternal UPD(20)", "MULCHANDANI-BHOJ-CONLIN SYNDROME", "Mulchandani-Bhoj-Conlin syndrome", "MULCHANDANI-BHOJ-CONLIN syndrome", "UNIPARENTAL DISOMY, MATERNAL, CHROMOSOME 20", "uniparental disomy, maternal, chromosome 20", "maternal uniparental disomy of chromosome 20", "Maternal uniparental disomy of chromosome 20", "maternal uniparental disomy of chromosome type 20", "Maternal UPD20 (uniparental disomy of chromosome 20)", "Maternal uniparental disomy of chromosome 20 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maternal uniparental disomy of chromosome 20", "shortest_name_length": 4}
{"curie": "UMLS:C1711276", "names": ["Lung Carcinosarcoma", "Carcinosarcoma of lung", "carcinosarcoma of lung", "Pulmonary Carcinosarcoma", "Carcinosarcoma of lung (disorder)", "carcinosarcoma of lung (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinosarcoma of lung", "shortest_name_length": 19}
{"curie": "MONDO:0011453", "names": ["ulnar ray dysgenesis with postaxial polydactyly and renal cystic dysplasia", "ULNAR RAY DYSGENESIS WITH POSTAXIAL POLYDACTYLY AND RENAL CYSTIC DYSPLASIA", "Ulnar Ray Dysgenesis with Postaxial Polydactyly and Renal Cystic Dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ulnar ray dysgenesis with postaxial polydactyly and renal cystic dysplasia", "shortest_name_length": 74}
{"curie": "MONDO:0044206", "names": ["OSMED", "OSMEDB", "WZS, FORMERLY", "NANCE-INSLEY SYNDROME", "Nance-Insley syndrome", "Insley-Astley syndrome", "Nance-Sweeney chondrodysplasia", "NANCE-SWEENEY CHONDRODYSPLASIA", "Nance Sweeney chondrodysplasia", "Nance-Sweeney Chondrodysplasia", "Weissenbacher-Zweymuller syndrome", "Otospondylomegaepiphyseal dysplasia", "Oto-Spondylo-Megaepiphyseal Dysplasia", "Oto-Spondylo-Mega-Epiphyseal Dysplasia", "Weissenbacher-Zweymuller syndrome, formerly", "WEISSENBACHER-ZWEYMULLER SYNDROME, FORMERLY", "CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS", "Chondrodystrophy with Sensorineural Deafness", "chondrodystrophy with sensorineural deafness", "OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE", "otospondylomegaepiphyseal dysplasia, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "otospondylomegaepiphyseal dysplasia, autosomal recessive", "shortest_name_length": 5}
{"curie": "MONDO:0008636", "names": ["OHVIRA syndrome", "Wunderlich syndrome", "Herlyn-Werner syndrome", "Herlyn Werner syndrome", "Double uterus-hemivagina-renal agenesis syndrome", "Double uterus and obstructed hemivagina syndrome", "double uterus-hemivagina-renal agenesis syndrome", "Double uterus, hemivagina, renal agenesis syndrome", "obstructed hemivagina and ipsilateral renal anomaly", "Obstructed hemivagina and ipsilateral renal anomaly", "Obstructed hemivagina and ipsilateral renal anomaly syndrome", "Double uterus, hemivagina, renal agenesis syndrome (disorder)", "UTERUS BICORNIS BICOLLIS WITH PARTIAL VAGINAL SEPTUM AND UNILATERAL HEMATOCOLPOS WITH IPSILATERAL RENAL AGENESIS", "uterus BICORNIS BICOLLIS with partial vaginal septum and unilateral HEMATOCOLPOS with ipsilateral renal agenesis", "Uterus Bicornis Bicollis With Partial Vaginal Septum And Unilateral Hematocolpos With Ipsilateral Renal Agenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "double uterus-hemivagina-renal agenesis syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0004041", "names": ["uPA", "Bladder wart", "bladder wart", "bladder warts", "Bladder papilloma", "bladder papilloma", "BLADDER PAPILLOMA", "papilloma bladder", "bladder; papilloma", "BLADDER, PAPILLOMA", "papilloma; bladder", "Papillomata;bladder", "bladder papillomata", "Papilloma of bladder", "Urothelial papilloma", "papilloma of bladder", "Urothelial Papilloma", "urothelial papilloma", "papilloma urinary bladder", "Urinary bladder papilloma", "Urothelial papilloma, NOS", "Papilloma of urinary bladder", "bladder transitional cell papilloma", "urinary bladder Urothelial papilloma", "transitional cell papilloma of bladder", "Urothelial papilloma (morphologic abnormality)", "Transitional cell papilloma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urothelial papilloma", "shortest_name_length": 3}
{"curie": "MONDO:0005454", "names": ["lung NET", "Bronchial NET", "lung neuroendocrine tumor", "lung neuroendocrine neoplasm", "Lung Neuroendocrine Neoplasm", "Bronchial neuroendocrine tumor", "pulmonary neuroendocrine tumor", "Bronchial neuroendocrine tumour", "Neuroendocrine neoplasm of lung", "Neuroendocrine Neoplasm of Lung", "neuroendocrine neoplasm of lung", "pulmonary neuroendocrine neoplasm", "Pulmonary Neuroendocrine Neoplasm", "neuroendocrine neoplasm of the lung", "Neuroendocrine Neoplasm of the Lung", "Neuroendocrine neoplasm of lung (disorder)", "lung neuroendocrine tumor, well differentiated, low or intermediate grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung neuroendocrine neoplasm", "shortest_name_length": 8}
{"curie": "UMLS:C1720811", "names": ["Rete Testis Tumor", "Testis Tumor, Rete", "Rete Testis Tumors", "Testis Tumors, Rete", "Tumor of Rete Testis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tumor of Rete Testis", "shortest_name_length": 17}
{"curie": "UMLS:C0574912", "names": ["Calyceal diverticulum", "Calyceal Diverticulum", "Acquired calyceal diverticulum", "Acquired calyceal diverticulum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired calyceal diverticulum", "shortest_name_length": 21}
{"curie": "MONDO:0012549", "names": ["ARCA1", "SCAR8", "Arca1", "recessive ataxia of Beauce", "Recessive Ataxia of Beauce", "ATAXIA, RECESSIVE, OF BEAUCE", "Ataxia, Recessive, of Beauce", "ataxia, recessive, of Beauce", "autosomal recessive ataxia Beauce type", "autosomal recessive ataxia, Beauce type", "Autosomal recessive ataxia, Beauce type", "spinocerebellar ataxia autosomal recessive 8", "Autosomal Recessive Cerebellar Ataxia Type 1", "autosomal recessive cerebellar ataxia type 1", "autosomal recessive spinocerebellar ataxia 8", "Autosomal recessive cerebellar ataxia type 1", "Autosomal Recessive Spinocerebellar Ataxia 8", "Spinocerebellar Ataxia, Autosomal Recessive 8", "spinocerebellar ataxia, autosomal recessive 8", "ARCA1 Autosomal Recessive Cerebellar Ataxia 1", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 8", "cerebellar ataxia, autosomal recessive, type 1", "Cerebellar Ataxia, Autosomal Recessive, Type 1", "CEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE, TYPE 1", "spinocerebellar ataxia, autosomal recessive type 8", "SCAR8 Spinocerebellar Ataxia, Autosomal Recessive 8", "SYNE1-related autosomal recessive cerebellar ataxia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive ataxia, Beauce type", "shortest_name_length": 5}
{"curie": "MONDO:0010613", "names": ["GKD", "gk deficiency", "GK deficiency", "GK DEFICIENCY", "GK1 DEFICIENCY", "GK1 deficiency", "hyperglycerolemia", "Hyperglycerolemia", "HYPERGLYCEROLEMIA", "Hyperglycerolaemia", "glycerol kinase syndrome", "Glycerol Kinase Deficiency", "Familial hyperglycerolemia", "Pseudohypertriglyceridemia", "glycerol kinase deficiency", "Glycerol kinase deficiency", "familial hyperglycerolemia", "GLYCEROL KINASE DEFICIENCY", "Familial hyperglycerolaemia", "Deficiency of glycerol kinase", "deficiency of glycerol kinase", "GKD - Glycerol kinase deficiency", "inborn glycerol kinase deficiency", "Isolated glycerol kinase deficiency", "Glycerol kinase deficiency - isolated", "inborn error of glycerol kinase activity", "inborn glycerol kinase activity disorder", "Deficiency of glycerol kinase (disorder)", "deficiency of glycerol kinase (diagnosis)", "rare inborn error of glycerol kinase activity", "glycerol kinase deficiency, X-linked recessive", "X-linked congenital glycerol kinase deficiency", "glycerol kinase (GK) deficiency (GKD) syndrome", "Glycerol kinase deficiency - isolated (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn glycerol kinase deficiency", "shortest_name_length": 3}
{"curie": "MONDO:0000949", "names": ["atrophy; conjunctiva", "conjunctiva; atrophy", "degeneration; conjunctiva", "conjunctival degeneration", "conjunctiva; degeneration", "Conjunctival degeneration", "Conjunctival degeneration, NOS", "Conjunctival degeneration (disorder)", "conjunctival degeneration (diagnosis)", "Unspecified conjunctival degenerations", "Conjunctival degeneration, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "conjunctival degeneration", "shortest_name_length": 20}
{"curie": "MONDO:0006760", "names": ["HDFN", "Fetal Erythroblastoses", "Fetal Erythroblastosis", "fetal erythroblastosis", "Erythroblastosis, Fetal", "Erythroblastosis Fetali", "Erythroblastoses, Fetal", "disease fetus hemolytic", "Fetali, Erythroblastosis", "Neonatal isoerythrolysis", "Erythroblastosis Fetalis", "Erythroblastosis fetalis", "erythroblastosis fetalis", "ERYTHROBLASTOSIS FETALIS", "ERYTHROBLASTOSIS, FETALIS", "Newborn Hemolytic Disease", "disease hemolytic newborn", "hemolytic disease newborn", "Erythroblastosis foetalis", "Fetalis, Erythroblastosis", "erythroblastosis foetalis", "icterus gravis neonatorum", "haemolytic disease newborn", "disease haemolytic newborn", "Isoimmunisation of newborn", "Disease;haemolytic;newborn", "disease hemolytic newborns", "diseases hemolytic newborn", "Isoimmunization of newborn", "Newborn Hemolytic Diseases", "disease haemolytic newborns", "ERYTHROBLASTOSIS NEONATORUM", "Hemolytic disease of newborn", "Erythroblastosis fetalis NOS", "hemolytic disease of newborn", "Hemolytic Disease of Newborn", "disease hemolytic of newborn", "HEMOLYTIC DISEASE, OF NEWBORN", "Erythroblastosis fetalis, NOS", "EF - Erythroblastosis fetalis", "EF - Erythroblastosis foetalis", "Erythroblastosis foetalis, NOS", "hemolytic disease of a newborn", "EF - erythroblastosis foetalis", "Hemolytic disease of fetus NOS", "haemolytic disease of a newborn", "Erythroblastosis neonatorum NOS", "hemolytic disease of the newborn", "Hemolytic disease of newborn NOS", "Erythroblastosis neonatorum, NOS", "Hemolytic disease of the newborn", "Hemolytic Disease of the Newborn", "Haemolytic disease of the newborn", "fetus or newborn; isoimmunization", "Hemolytic disease of fetus OR newborn", "rhesus isoimmunisation of the newborn", "fetal hemolysis due to isoimmunization", "HDN - Hemolytic disease of the newborn", "Hemolytic disease of fetus and newborn", "HDN - Haemolytic disease of the newborn", "Haemolytic disease of fetus and newborn", "Haemolytic disease of foetus OR newborn", "Alloimmune hemolytic disease of newborn", "hemolytic disease of newborn (diagnosis)", "Alloimmune haemolytic disease of newborn", "Hemolytic disease of newborn, unspecified", "Hemolytic Disease of the Fetus or Newborn", "hemolytic disease of the fetus or newborn", "Hemolytic disease of fetus or newborn, NOS", "Hemolytic disease of the fetus and newborn", "Isoimmune Hemolytic Disease of the Newborn", "isoimmune hemolytic disease of the newborn", "Haemolytic disease of foetus or newborn, NOS", "Haemolytic disease due to rhesus isoimmunisation", "haemolytic disease due to rhesus isoimmunisation", "fetal or neonatal hemolysis due to isoimmunization", "fetal hemolysis due to isoimmunization (diagnosis)", "Hemolytic disease of fetus and newborn, unspecified", "Haemolytic disease of fetus and newborn, unspecified", "Hemolytic disease due to fetomaternal alloimmunization", "Hemolytic disease of fetus OR newborn due to isoimmunization", "Hemolytic disease of fetus or newborn, due to isoimmunization", "Haemolytic disease of fetus OR newborn due to isoimmunisation", "Hemolytic disease of fetus and newborn due to isoimmunization", "Haemolytic disease of fetus and newborn due to isoimmunisation", "Haemolytic disease of foetus OR newborn due to isoimmunisation", "fetal or neonatal hemolysis due to isoimmunization (diagnosis)", "Haemolytic disease of foetus or newborn, due to isoimmunisation", "Hemolytic disease of fetus or newborn due to isoimmunization, NOS", "Haemolytic disease of foetus or newborn due to isoimmunization, NOS", "Hemolytic disease of fetus OR newborn due to isoimmunization (disorder)", "Hemolytic disease of fetus or newborn due to other and unspecified isoimmunization"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fetal erythroblastosis", "shortest_name_length": 4}
{"curie": "MONDO:0015031", "names": ["extraneural perineurioma", "Soft tissue perineurioma", "soft tissue perineurioma", "Extraneural perineurioma", "Extraneural perineurioma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extraneural perineurioma", "shortest_name_length": 24}
{"curie": "UMLS:C0847403", "names": ["tenosynovitis infective", "Infective tenosynovitis", "tenosynovitis; infective", "infective; tenosynovitis", "tenosynovitis infective (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infective tenosynovitis", "shortest_name_length": 23}
{"curie": "UMLS:C1514835", "names": ["Renal Cell Carcinoma with Constitutional Chromosome 3 Translocations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal Cell Carcinoma with Constitutional Chromosome 3 Translocations", "shortest_name_length": 68}
{"curie": "MONDO:0060532", "names": ["CHDSKM", "congenital heart defects and skeletal malformations syndrome", "CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital heart defects and skeletal malformations syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0100022", "names": ["neonatal/infantile epilepsy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal/infantile epilepsy syndrome", "shortest_name_length": 36}
{"curie": "UMLS:C4521863", "names": ["Stage I Ampulla of Vater Cancer", "Stage I Ampulla of Vater Cancer AJCC v8", "Stage I Ampulla of Vater Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Ampulla of Vater Cancer AJCC v8", "shortest_name_length": 31}
{"curie": "MONDO:0001884", "names": ["abducens nerve tumor", "Abducens Nerve Tumor", "Abducens Nerve Tumors", "abducens nerve tumors", "Abducens Nerve Neoplasm", "abducens nerve neoplasm", "Tumor of Abducens Nerve", "tumor of abducens nerve", "abducens nerve neoplasms", "Abducens Nerve Neoplasms", "VIth Cranial Nerve Tumors", "VIth cranial nerve tumors", "sixth cranial nerve tumor", "Sixth Cranial Nerve Tumor", "VIth Cranial nerve tumors", "Neoplasm of abducens nerve", "sixth cranial nerve tumors", "Sixth Cranial Nerve Tumors", "Neoplasm of Abducens Nerve", "neoplasm of abducens nerve", "tumor of the abducens nerve", "Tumor of the Abducens Nerve", "VIth cranial nerve neoplasms", "Sixth Cranial Nerve Neoplasm", "sixth cranial nerve neoplasm", "VIth Cranial Nerve Neoplasms", "Tumor of Sixth Cranial Nerve", "tumor of sixth cranial nerve", "Sixth Cranial Nerve Neoplasms", "sixth cranial nerve neoplasms", "Neoplasm of the Abducens Nerve", "neoplasm of the abducens nerve", "Neoplasm of Sixth Cranial Nerve", "neoplasm of sixth cranial nerve", "Tumor of the Sixth Cranial Nerve", "tumor of the sixth cranial nerve", "abducens nerve neoplasm (disease)", "neoplasm of the sixth cranial nerve", "Neoplasm of the Sixth Cranial Nerve", "Neoplasm of abducens nerve (disorder)", "neoplasm of sixth cranial nerve (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "abducens nerve neoplasm", "shortest_name_length": 20}
{"curie": "MONDO:0015428", "names": ["Moloney syndrome", "Choroidal atrophy alopecia", "choroidal atrophy alopecia", "Choroidal atrophy-alopecia syndrome", "choroidal atrophy-alopecia syndrome", "choroidal atrophy and alopecia syndrome", "Choroidal atrophy and alopecia syndrome", "regional choroidal atrophy and alopecia", "Regional choroidal atrophy and alopecia", "Choroidal atrophy and alopecia syndrome (disorder)", "choroidal atrophy and alopecia syndrome (diagnosis)", "fine hair, absent/decreased lashes, absent/decreased eyebrows, visual loss-mild/suspected, dysplastic/thick/grooved toenails and fingernails"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choroidal atrophy-alopecia syndrome", "shortest_name_length": 16}
{"curie": "UMLS:C5206797", "names": ["Metastatic Gallbladder Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Gallbladder Carcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C0280479", "names": ["good prognosis metastatic GTT", "metastatic GTT, good prognosis", "GTT, metastatic, good prognosis", "GTT, good prognosis, metastatic", "trophoblastic tumor, metastatic, good prognosis", "low risk metastatic gestational trophoblastic tumor", "Good Prognosis Metastatic Gestational Trophoblastic Tumor", "good prognosis metastatic gestational trophoblastic tumor", "gestational trophoblastic tumor, good prognosis, metastatic", "gestational trophoblastic tumor, metastatic, good prognosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Good Prognosis Metastatic Gestational Trophoblastic Tumor", "shortest_name_length": 29}
{"curie": "MONDO:0016622", "names": ["Melhem Fahl syndrome", "Melhem-Fahl syndrome", "Melhem Fahl syndrome (disorder)", "fifteen dorsal vertebrae and rib pairs", "Fifteen dorsal vertebrae and rib pairs"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Melhem-Fahl syndrome", "shortest_name_length": 20}
{"curie": "MONDO:0013522", "names": ["DKCA3", "autosomal dominant dyskeratosis congenita 3", "DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 3", "Dyskeratosis Congenita, Autosomal Dominant 3", "dyskeratosis congenita, autosomal dominant 3", "DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 3", "dyskeratosis congenita, autosomal dominant type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyskeratosis congenita, autosomal dominant 3", "shortest_name_length": 5}
{"curie": "MONDO:0018873", "names": ["ACNES", "rectus abdominis syndrome", "intercostal nerve syndrome", "anterior cutaneous nerve entrapment syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anterior cutaneous nerve entrapment syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0000675", "names": ["analgesia", "Analgesia", "pain agnosia", "Pain Agnosia", "Agnosia for Pain", "Agnosia for pain", "Agnosia for pain (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pain agnosia", "shortest_name_length": 9}
{"curie": "UMLS:C5556544", "names": ["LGPSC", "Low-Grade Papillary Sinonasal Carcinoma", "Low Grade Papillary Sinonasal Carcinoma", "Low Grade Papillary Schneiderian Carcinoma", "Low-Grade Papillary Schneiderian Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Grade Papillary Schneiderian Carcinoma", "shortest_name_length": 5}
{"curie": "UMLS:C4763562", "names": ["Borderline Resectable Pancreatic Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Resectable Pancreatic Adenocarcinoma", "shortest_name_length": 47}
{"curie": "UMLS:C2828012", "names": ["Stage IB Merkel Cell Carcinoma", "Stage IB Merkel Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Merkel Cell Carcinoma AJCC v7", "shortest_name_length": 30}
{"curie": "MONDO:0031012", "names": ["autoimmune uveitis", "autoimmune uveitis (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune uveitis", "shortest_name_length": 18}
{"curie": "UMLS:C4761244", "names": ["Gastroesophageal burn", "Gastroesophageal Burn", "Gastrooesophageal burn"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastroesophageal burn", "shortest_name_length": 21}
{"curie": "MONDO:0035529", "names": ["OAS1 deficiency", "infantile-onset pulmonary alveolar proteinosis-hypogammaglobulinemia", "OAS1-related infantile-onset pulmonary alveolar proteinosis-hypogammaglobulinemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile-onset pulmonary alveolar proteinosis-hypogammaglobulinemia", "shortest_name_length": 15}
{"curie": "UMLS:C1268936", "names": ["D+ HUS", "Stx-HUS", "EHEC-HUS", "STEC-HUS", "Typical HUS", "Diarrhea-associated HUS", "Shiga-like toxin-associated HUS", "Classic hemolytic uremic syndrome", "Typical hemolytic uremic syndrome", "Epidemic hemolytic uremic syndrome", "Classic haemolytic uraemic syndrome", "Epidemic haemolytic uraemic syndrome", "Hemolytic uremic syndrome with diarrhea", "Diarrhea-associated Hemolytic Uremic Syndrome", "Diarrhea-associated hemolytic uremic syndrome", "Diarrhea-associated haemolytic uraemic syndrome", "Shiga toxin-associated hemolytic uremic syndrome", "Diarrhea-associated hemolytic uremic syndrome (disorder)", "Hemolytic uremic syndrome associated with Shiga toxin-producing Escherichia coli"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diarrhea-associated hemolytic uremic syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C4553576", "names": ["Stage III Thyroid Gland Follicular Cancer", "Stage III Thyroid Gland Follicular Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Thyroid Gland Follicular Carcinoma AJCC v8", "shortest_name_length": 41}
{"curie": "MONDO:0001540", "names": ["Bagassosis", "BAGASSOSIS", "bagassosis", "Bagasse disease", "bagasse workers lung", "Bagassosis (disorder)", "Bagasse workers' lung", "bagassosis (diagnosis)", "Bagasse workers' disease", "sugar cane worker pneumonitis", "bagasse disease or pneumonitis", "fibrosis; lung, with bagassosis", "lung; fibrosis, with bagassosis", "bagasse extrinsic allergic alveolitis", "extrinsic allergic alveolitis from bagasse", "pneumonitis; hypersensitivity, with bagassosis", "hypersensitivity; pneumonitis, with bagassosis", "Sugar cane workers' hypersensitivity pneumonitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bagassosis", "shortest_name_length": 10}
{"curie": "UMLS:C0264588", "names": ["spastic dysphonia", "Spastic dysphonia", "dysphonia spastic", "Spastic Dysphonia", "SPASTIC DYSPHONIAS", "spastic; dysphonia", "dysphonia; spastic", "Dystonic dysphonia", "Dysphonia, Spastic", "spasmodic dysphonia", "Spasmodic dysphonia", "dysphonia spasmodic", "Dysphonia, spasmodic", "Spastic dysphonia, NOS", "speech phonation spastic", "Spastic dysphonia (disorder)", "spastic dysphonia was observed", "spastic dysphonia (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spastic Dysphonia", "shortest_name_length": 17}
{"curie": "MONDO:0001244", "names": ["Hypovitaminosis K", "k vitamin deficiency", "Vitamin K Deficiency", "deficiency vitamin k", "VITAMIN K DEFICIENCY", "Vitamin K deficiency", "vitamin k deficiency", "vitamin K deficiency", "deficiency k vitamin", "deficiency; vitamin K", "Deficiency, Vitamin K", "vitamin k deficiencies", "Vitamin K Deficiencies", "deficiencies k vitamin", "Low levels of vitamin K", "deficiency of vitamin K", "Deficiency of vitamin K", "deficiency of vitamin k", "Deficiencies, Vitamin K", "of vitamin k deficiency", "Vitamin K deficiency disease", "disease vitamin k deficiency", "vitamin K deficiency bleeding", "Vitamin K deficiency (disorder)", "vitamin K deficiency (diagnosis)", "vitamin K deficiency hemorrhagic disease", "vitamin K deficiency coagulation disorder", "Vitamin K deficiency coagulation disorder", "Vitamin K Deficiency Coagulation Disorder", "Vitamin K deficiency coagulation disorder, NOS", "Bleeding diathesis due to vitamin K deficiency", "Vitamin K deficiency coagulation disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitamin K deficiency hemorrhagic disease", "shortest_name_length": 17}
{"curie": "MONDO:0012761", "names": ["Trisomy 3q29", "trisomy 3q29", "3q29 microduplication", "MICRODUPLICATION 3q29 SYNDROME", "Microduplication 3q29 Syndrome", "microduplication 3Q29 syndrome", "3q29 microduplication syndrome", "Chromosome 3q29 Duplication Syndrome", "Chromosome 3q29 duplication syndrome", "chromosome 3q29 DUPLICATION syndrome", "CHROMOSOME 3q29 DUPLICATION SYNDROME", "chromosome 3q29 microduplication syndrome", "Chromosome 3q29 duplication syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 3q29 microduplication syndrome", "shortest_name_length": 12}
{"curie": "UMLS:C0334356", "names": ["Borderline Papillary Cystadenoma", "Borderline Malignancy Papillary Cystadenoma", "Papillary cystadenoma, borderline malignancy", "Papillary cystadenoma - borderline malignancy", "Low Malignancy Potential Papillary Cystadenoma", "[M] Papillary cystadenoma, borderline malignancy", "borderline malignancy; papillary cystadenoma, unspecified site", "papillary; cystadenoma, borderline malignancy, unspecified site", "cystadenoma; papillary, borderline malignancy, unspecified site", "Papillary cystadenoma, borderline malignancy (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Papillary cystadenoma, borderline malignancy", "shortest_name_length": 32}
{"curie": "MONDO:0044984", "names": ["nasolacrimal duct disease", "nasolacrimal duct disorder", "disease of nasolacrimal duct", "disorder of nasolacrimal duct", "Disorder of nasolacrimal duct", "Disorder of nasolacrimal duct, NOS", "nasolacrimal duct disease or disorder", "Disorder of nasolacrimal duct (disorder)", "disease or disorder of nasolacrimal duct"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasolacrimal duct disorder", "shortest_name_length": 25}
{"curie": "MONDO:0015127", "names": ["pituitary deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pituitary deficiency", "shortest_name_length": 20}
{"curie": "MONDO:0001396", "names": ["abnormal threshold of rods", "Abnormal threshold of rods", "Delayed adaptation of rods", "Dark adaptation abnormality", "Abnormal threshold of cones", "Delayed adaptation of cones", "Abnormal dark adaptation curve", "abnormal dark adaptation curve", "Abnormal dark adaptation curve (disorder)", "abnormal dark adaptation curve (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "abnormal threshold of rods", "shortest_name_length": 26}
{"curie": "MONDO:0009481", "names": ["Jumping disease", "'jumpers' of Maine", "Jumping disease (disorder)", "Jumping Frenchmen of Maine", "JUMPING FRENCHMEN OF MAINE", "exaggerated startle reflex", "jumping Frenchmen of Maine", "Jumping disease (diagnosis)", "psychiatric disorders neurosis jumping disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jumping Frenchmen of Maine", "shortest_name_length": 15}
{"curie": "UMLS:C1336262", "names": ["Stage III Ovarian Polyembryoma", "Ovarian Polyembryoma Stage III", "Stage III Ovarian Polyembryoma AJCC v6", "Stage III Ovarian Polyembryoma AJCC v7", "Stage III Ovarian Polyembryoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Ovarian Polyembryoma AJCC v6 and v7", "shortest_name_length": 30}
{"curie": "MONDO:0005106", "names": ["Lipoma", "LIPOMA", "lipoma", "lipomas", "Lipomas", "lipomata", "Lipomata", "Lipomatas", "Fatty lump", "lipoma nos", "Lipoma NOS", "fatty tumor", "Fatty Tumor", "Lipoma, NOS", "Tumor, Fatty", "fatty tumors", "Fatty Tumors", "Tumors, Fatty", "LIPOMA, BENIGN", "lipoma, benign", "lipomatous tumor", "Lipomatous tumor", "Lipoma (clinical)", "Lipoma morphology", "Lipoma (disorder)", "lipoma (diagnosis)", "Lipomatous neoplasm", "lipomatous neoplasm", "multiple lipomatosis", "benign lipomatous tumor", "Noncancerous fatty lump", "tumor of adipose tissue", "Lipoma, unspecified site", "benign tumor of adipose tissue", "LIPOMATOSIS, FAMILIAL MULTIPLE", "benign tumor of Adipose tissue", "lipomatosis, familial multiple", "Lipoma of unspecified body site", "Lipoma morphology (morphologic abnormality)", "lipomatous neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lipoma", "shortest_name_length": 6}
{"curie": "MONDO:0000276", "names": ["Powassan encephalitis", "Powassan Encephalitis", "encephalitis; Powassan", "Powassan virus disease", "encephalitis, powassan", "Powassan; encephalitis", "Encephalitis, Powassan", "Powassan Virus Disease", "Powassan Encephalitides", "Virus Disease, Powassan", "Powassan Virus Diseases", "Disease, Powassan Virus", "Virus Diseases, Powassan", "Powassan viral encephalitis", "Powassan tick-borne encephalitis", "Powassan encephalitis (diagnosis)", "Powassan virus infectious disease", "Powassan virus disease or disorder", "Powassan encephalitis virus infection", "powassan encephalitis virus infection", "Powassan virus caused disease or disorder", "Powassan encephalitis virus infection (disorder)", "Neuroinvasive Powassan encephalitis virus infection", "Neuroinvasive Powassan encephalitis virus infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Powassan encephalitis", "shortest_name_length": 21}
{"curie": "MONDO:0002195", "names": ["vulvar squamous tumor", "Vulvar Squamous Tumor", "vulvar squamous neoplasm", "Vulvar Squamous Neoplasm", "mammalian vulva squamous cell neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar squamous neoplasm", "shortest_name_length": 21}
{"curie": "MONDO:0012780", "names": ["CELIAC11", "celiac disease, susceptibility to, 11", "CELIAC DISEASE, SUSCEPTIBILITY TO, 11", "GLUTEN-SENSITIVE ENTEROPATHY, SUSCEPTIBILITY TO, 11", "gluten-sensitive enteropathy, susceptibility to, 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "celiac disease, susceptibility to, 11", "shortest_name_length": 8}
{"curie": "UMLS:C0276496", "names": ["EOFAD", "familial alzheimer disease", "Familial Alzheimer disease", "familial Alzheimer disease", "Alzheimer disease familial", "Familial Alzheimer's disease", "familial alzheimer's disease", "Familial Alzheimer Disease (FAD)", "familial Alzheimer disease (FAD)", "Alzheimer Disease, Familial (FAD)", "Familial Alzheimer Diseases (FAD)", "familial Alzheimer disease (diagnosis)", "Early-onset autosomal dominant Alzheimer disease", "Early-onset familial autosomal dominant Alzheimer disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Familial Alzheimer Disease (FAD)", "shortest_name_length": 5}
{"curie": "MONDO:0015519", "names": ["congenital or early infantile CACH syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital or early infantile CACH syndrome", "shortest_name_length": 43}
{"curie": "UMLS:C5420230", "names": ["Moderate ARDS", "Moderate Acute Respiratory Distress Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Moderate Acute Respiratory Distress Syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0008968", "names": ["Cholestasis with Gallstone, Ataxia, and Visual Disturbance", "CHOLESTASIS WITH GALLSTONE, ATAXIA, AND VISUAL DISTURBANCE", "cholestasis with gallstone, ataxia, and visual disturbance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholestasis with gallstone, ataxia, and visual disturbance", "shortest_name_length": 58}
{"curie": "UMLS:C5206691", "names": ["Recurrent Adamantinomatous Craniopharyngioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Adamantinomatous Craniopharyngioma", "shortest_name_length": 44}
{"curie": "MONDO:0018070", "names": ["familial multiple fibrofolliculoma", "multiple fibrofolliculoma familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial multiple fibrofolliculoma", "shortest_name_length": 34}
{"curie": "MONDO:0016420", "names": ["familial flecked retinopathy", "hereditary flecked retinopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial flecked retinopathy", "shortest_name_length": 28}
{"curie": "MONDO:0032773", "names": ["URCTU", "uridine-cytidineuria", "URIDINE-CYTIDINEURIA", "Uridine-cytidineuria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uridine-cytidineuria", "shortest_name_length": 5}
{"curie": "MONDO:0004753", "names": ["Mechanical Strabismus", "mechanical strabismus", "Mechanical strabismus", "strabismus; mechanical", "Strabismus, mechanical", "Strabismus, Mechanical", "mechanical; strabismus", "Mechanical strabismus, NOS", "Mechanical strabismus (disorder)", "mechanical strabismus (diagnosis)", "Mechanical strabismus, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mechanical strabismus", "shortest_name_length": 21}
{"curie": "UMLS:C3898157", "names": ["Sinonasal Small Cell Carcinoma", "Sinonasal Small Cell Neuroendocrine Carcinoma", "Nasal Cavity and Paranasal Sinus Small Cell Carcinoma", "Nasal Cavity and Paranasal Sinus Small Cell Neuroendocrine Cancer", "Nasal Cavity and Paranasal Sinus Small Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Small Cell Neuroendocrine Carcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0013991", "names": ["LEPD", "morbid obesity", "OBESITY, MORBID", "LEPTIN DEFICIENCY", "Leptin Deficiency", "congenital leptin deficiency", "Congenital leptin deficiency", "obesity, morbid, nonsyndromic 1", "leptin deficiency or dysfunction", "LEPTIN DEFICIENCY OR DYSFUNCTION", "Congenital leptin deficiency (disorder)", "obesity, morbid, due to leptin deficiency", "Obesity due to congenital leptin deficiency", "obesity due to congenital leptin deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "obesity due to congenital leptin deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0001147", "names": ["MENINGOCELE", "meningocele", "Meningocele", "Meningoceles", "meningoceles", "Meningocele, NOS", "spinal meningocele", "Spinal meningocele", "Spinal Meningocele", "Meninges Herniation", "Meninges Herniations", "meningocele (spinal)", "Meningeal Herniation", "meningocele (disease)", "Herniation, Meningeal", "Meningeal Herniations", "Congenital meningocele", "Herniations, Meningeal", "Herniation of Meninges", "Meningocele (disorder)", "Congenital meningocele, NOS", "Congenital hydromeningocele", "Congenital spinal meningocele", "Congenital hernia of dura mater", "Congenital meningocele (disorder)", "Congenital spinal hydromeningocele", "central nervous system meningocele", "Central Nervous System Meningocele", "Congenital spinal meningocele (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "meningocele", "shortest_name_length": 11}
{"curie": "MONDO:0000446", "names": ["midface dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "midface dysplasia", "shortest_name_length": 17}
{"curie": "MONDO:0024981", "names": ["rodent disease", "Rodent Disease", "diseases rodent", "rodent diseases", "Disease, Rodent", "disease, Rodent", "Rodent Diseases", "Diseases, Rodent", "diseases, Rodent", "diseases rodents", "Rodents--Diseases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rodent disease", "shortest_name_length": 14}
{"curie": "UMLS:C4745066", "names": ["Metastatic Unresectable Basal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Unresectable Basal Cell Carcinoma", "shortest_name_length": 44}
{"curie": "MONDO:0009436", "names": ["PHLS", "Hypothalamic hamartoma", "Hypothalamic Hamartoma", "hypothalamic hamartoma", "hypothalamic hamartomas", "Hypothalamic hamartomas", "Tuber cinereum hamartoma", "Hamartoma of hypothalamus", "Hamartoma of Hypothalamus", "hamartoma of hypothalamus", "Pallister-Hall-like syndrome", "PALLISTER-HALL-LIKE SYNDROME", "hamartoma of the hypothalamus", "Hamartoma of the hypothalamus", "Hamartoma of the Hypothalamus", "Hamartoma of hypothalamus (disorder)", "hamartoma of hypothalamus (diagnosis)", "congenital hypothalamic hamartoma syndrome", "Congenital hypothalamic hamartoma syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital hypothalamic hamartoma syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0013098", "names": ["NIHL", "Noise Induced Hearing Loss", "Noise-induced hearing loss", "Noise-Induced Hearing Loss", "noise-induced hearing loss", "Noise induced hearing loss", "noise induced hearing loss", "hearing induced loss noise", "hearing loss noise induced", "Hearing Loss, Noise Induced", "Hearing Loss, Noise-Induced", "loss; hearing, noise-induced", "hearing; loss, noise-induced", "HEARING DISORDER, NOISE-INDUCED", "NIHL - Noise-induced hearing loss", "Noise-induced hearing loss (disorder)", "noise induced hearing loss (diagnosis)", "hearing loss, noise-induced, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "noise induced hearing loss", "shortest_name_length": 4}
{"curie": "UMLS:C0206740", "names": ["Gorlin Cyst", "Calcifying Odontogenic Cyst", "Calcifying odontogenic cyst", "cyst; calcifying odontogenic", "Cyst, Calcifying Odontogenic", "calcifying; odontogenic cyst", "Odontogenic Cyst, Calcifying", "Calcifying Odontogenic Cysts", "calcifying; cyst, odontogenic", "Cysts, Calcifying Odontogenic", "Odontogenic Cysts, Calcifying", "Calcifying Cystic Odontogenic Tumor", "Calcifying odontogenic cyst (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Calcifying Odontogenic Cyst", "shortest_name_length": 11}
{"curie": "MONDO:0011986", "names": ["TCP", "Tropical pancreatitis", "tropical pancreatitis", "tropical calcific pancreatitis", "Tropical Calcific Pancreatitis", "TROPICAL CALCIFIC PANCREATITIS", "Tropical calcific chronic pancreatitis", "tropical calcific chronic pancreatitis", "Tropical calcific chronic pancreatitis (disorder)", "fibrocalculous pancreatic diabetes, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tropical pancreatitis", "shortest_name_length": 3}
{"curie": "UMLS:C3203357", "names": ["TB bone", "TB of the bone", "Tuberculous bone", "Bone Tuberculosis", "Bone Tuberculoses", "tuberculosis bone", "bone tuberculosis", "Bone tuberculosis", "tuberculosis bones", "bones tuberculoses", "bones tuberculosis", "Tuberculosis, Bone", "Tuberculoses, Bone", "Bones--Tuberculosis", "tuberculosis of bone", "of tuberculosis bone", "Tuberculosis;bone(s)", "Tuberculosis of bone", "Tuberculous osteitis", "tuberculosis skeletal", "skeletal tuberculosis", "Tuberculous osteomyelitis", "Tuberculosis of bone, NOS", "Tuberculosis of bone (disorder)", "tuberculosis of bone (diagnosis)", "skeletal tuberculosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone Tuberculosis", "shortest_name_length": 7}
{"curie": "MONDO:0004863", "names": ["Purulent endophthalmitis", "purulent endophthalmitis", "endophthalmitis; purulent", "purulent; endophthalmitis", "Purulent endophthalmitis, NOS", "Purulent endophthalmitis (disorder)", "purulent endophthalmitis (diagnosis)", "Unspecified purulent endophthalmitis", "Purulent endophthalmitis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "purulent endophthalmitis", "shortest_name_length": 24}
{"curie": "MONDO:0018758", "names": ["familial patent arterial duct"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial patent arterial duct", "shortest_name_length": 29}
{"curie": "UMLS:C1516700", "names": ["Colon Cancer by Astler-Coller Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colon Cancer by Astler-Coller Stage", "shortest_name_length": 35}
{"curie": "MONDO:0003197", "names": ["Granular Cell Carcinoma", "Granular cell carcinoma", "granular cell carcinoma", "Granular Cell Carcinomas", "Carcinoma, Granular Cell", "Carcinomas, Granular Cell", "granular cell adenocarcinoma", "Granular Cell Adenocarcinoma", "Granular cell adenocarcinoma", "Granular Cell Adenocarcinomas", "Adenocarcinoma, Granular Cell", "Adenocarcinomas, Granular Cell", "granular cell carcinoma (diagnosis)", "Granular cell carcinoma (morphologic abnormality)", "granular cell carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "granular cell carcinoma", "shortest_name_length": 23}
{"curie": "MONDO:0009581", "names": ["Belgian type mental retardation syndrome", "Mental retardation syndrome Belgian type", "mental retardation syndrome, Belgian type", "Mental retardation syndrome, Belgian type", "MENTAL RETARDATION SYNDROME, BELGIAN TYPE", "Belgian type intellectual disability syndrome", "intellectual disability syndrome, Belgian type", "intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome", "Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome", "intellectual disability, craniofacial dysmorphism, hypogonadism, diabetes mellitus syndrome", "Intellectual disability, craniofacial dysmorphism, hypogonadism, diabetes mellitus syndrome", "Intellectual disability, craniofacial dysmorphism, hypogonadism, diabetes mellitus syndrome (disorder)", "intellectual disability, craniofacial dysmorphism, hypogonadism, diabetes mellitus syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome", "shortest_name_length": 40}
{"curie": "MONDO:0018013", "names": ["C3 glomerulopathy", "non-Ig-mediated MPGN", "non-immunoglobulin-mediated MPGN", "non-Ig-mediated membranoproliferative glomerulonephritis", "non-immunoglobulin-mediated membranoproliferative glomerulonephritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-immunoglobulin-mediated membranoproliferative glomerulonephritis", "shortest_name_length": 17}
{"curie": "MONDO:0010797", "names": ["Pearson syndrome", "Pearson Syndrome", "Pearson's syndrome", "Pearson syndrome (diagnosis)", "Pearson's syndrome (disorder)", "PEARSON MARROW-PANCREAS SYNDROME", "Pearson Marrow-Pancreas Syndrome", "Pearson marrow-pancreas syndrome", "Pearson's marrow-pancreas syndrome", "Pearson's marrow/pancreas syndrome", "Sideroblastic anemia with marrow cell vacuolization and exocrine pancreatic dysfunction", "SIDEROBLASTIC ANEMIA WITH MARROW CELL VACUOLIZATION AND EXOCRINE PANCREATIC DYSFUNCTION", "sideroblastic Anemia with marrow cell vacuolization and exocrine pancreatic dysfunction", "sideroblastic anemia with marrow cell vacuolization and exocrine pancreatic dysfunction (formerly)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pearson syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0005927", "names": ["Polyomavirus infection", "Polyomavirus Infection", "Polyoma virus infection", "Polyomavirus infections", "Polyomavirus Infections", "Disease due to Polyomavirus", "Disease due to Polyomaviridae", "Disease caused by Polyomavirus", "Polyomavirus infectious disease", "polyomavirus infectious disease", "Disease due to Polyomavirus, NOS", "Disease caused by Polyomaviridae", "Disease caused by Polyomavirus (disorder)", "Disease caused by Polyomaviridae (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyomavirus infectious disease", "shortest_name_length": 22}
{"curie": "MONDO:0042980", "names": ["Westphal disease", "HD- Westphal variant", "Westphal variant of Huntington's disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Westphal disease", "shortest_name_length": 16}
{"curie": "MONDO:0012314", "names": ["SQT3", "Short QT Syndrome 3", "SHORT QT SYNDROME 3", "short QT syndrome 3", "KCNJ2 short QT syndrome", "short QT syndrome type 3", "short QT syndrome caused by mutation in KCNJ2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short QT syndrome type 3", "shortest_name_length": 4}
{"curie": "UMLS:C4722276", "names": ["ASK", "Anaplastic Sarcoma of the Kidney"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anaplastic Sarcoma of the Kidney", "shortest_name_length": 3}
{"curie": "MONDO:0002868", "names": ["Biliary Cystadenocarcinoma", "biliary cystadenocarcinoma", "Biliary cystadenocarcinoma", "Bile duct cystadenocarcinoma", "Bile Duct Cystadenocarcinoma", "bile duct cystadenocarcinoma", "cystadenocarcinoma; bile duct", "bile duct; cystadenocarcinoma", "cystadenocarcinoma of bile duct", "Cystadenocarcinoma of Bile Duct", "cystadenocarcinoma of the bile duct", "Cystadenocarcinoma of the Bile Duct", "Intrahepatic bile duct cystadenocarcinoma", "cystadenocarcinoma of bile duct (diagnosis)", "Bile Duct MCN with an Associated Invasive Carcinoma", "liver neoplasm malignant bile duct cystadenocarcinoma", "Bile duct cystadenocarcinoma (morphologic abnormality)", "bile duct cystadenocarcinoma (morphologic abnormality)", "bile duct mucinous cystic neoplasm with an associated invasive carcinoma", "Bile Duct Mucinous Cystic Neoplasm with an Associated Invasive Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bile duct mucinous cystic neoplasm with an associated invasive carcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0005708", "names": ["Mountain fever", "mountain fever", "FEVER, MOUNTAIN", "mountain; fever", "fever; mountain", "colorado fever tick", "Colorado Tick Fever", "colorado tick fever", "COLORADO TICK FEVER", "mountain tick fever", "Colorado tick fever", "Mountain tick fever", "FEVER, MOUNTAIN TICK", "Tick Fever, Colorado", "fever; Colorado tick", "Tick fever, Colorado", "Colorado tick; fever", "Fever, Colorado Tick", "American mountain fever", "CTF - Colorado tick fever", "Colorado tick encephalitis", "tick-borne; fever, Colorado", "Colorado tick-borne disease", "fever; tick-borne, Colorado", "American mountain tick fever", "American; mountain tick fever", "fever; American mountain tick", "mountain tick fever; American", "Tick fever, American mountain", "Colorado tick fever (disorder)", "Colorado tick fever (diagnosis)", "American mountain tick fever (diagnosis)", "tick-borne; fever, American mountain tick", "fever; tick-borne, American mountain tick", "Colorado tick fever virus infectious disease", "Colorado tick fever virus disease or disorder", "fever; mountain, American mountain tick (virus)", "mountain; fever, American mountain tick (virus)", "Colorado tick fever virus caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorado tick fever", "shortest_name_length": 14}
{"curie": "MONDO:0006133", "names": ["cervical adenoid cystic cancer", "Cervical Adenoid Cystic Cancer", "Cervix Adenoid Cystic Carcinoma", "Cervical Adenoid Cystic Carcinoma", "Cervical adenoid cystic carcinoma", "cervical adenoid cystic carcinoma", "Adenoid Cystic Carcinoma of Cervix", "adenoid cystic carcinoma of cervix", "cervix uteri adenoid cystic carcinoma", "Cervix Uteri Adenoid Cystic Carcinoma", "Adenoid Cystic Carcinoma of the Cervix", "adenoid cystic carcinoma of the cervix", "Uterine Cervix Adenoid Cystic Carcinoma", "uterine cervix adenoid cystic carcinoma", "Adenoid Cystic Carcinoma of Cervix Uteri", "adenoid cystic carcinoma of cervix uteri", "Adenoid cystic carcinoma of cervix uteri", "Adenoid Cystic Carcinoma of Uterine Cervix", "adenoid cystic carcinoma of uterine cervix", "adenoid cystic carcinoma of the cervix uteri", "adenoid cystic carcinoma of the Cervix Uteri", "Adenoid Cystic Carcinoma of the Cervix Uteri", "Adenoid cystic carcinoma of the cervix uteri", "Adenoid Cystic Carcinoma of the Uterine Cervix", "adenoid cystic carcinoma of cervix (diagnosis)", "adenoid cystic carcinoma of the uterine cervix", "Adenoid cystic carcinoma of cervix uteri (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical adenoid cystic carcinoma", "shortest_name_length": 30}
{"curie": "UMLS:C4684948", "names": ["Skin squamous cell carcinoma recurrent", "Recurrent Skin Squamous Cell Carcinoma", "Recurrent Cutaneous Squamous Cell Carcinoma", "recurrent squamous cell carcinoma of the skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin squamous cell carcinoma recurrent", "shortest_name_length": 38}
{"curie": "MONDO:0005893", "names": ["PanNEC", "pancreatic NEC", "Pancreatic NEC", "islet cell cancer", "pancreatic NEC G3", "Islet Cell Cancer", "islet cell carcinoma", "Islet Cell Carcinoma", "Islet cell carcinoma", "Carcinoma, Islet Cell", "Islet Cell Carcinomas", "Carcinomas, Islet Cell", "Islet cell adenocarcinoma", "Malignant Islet Cell Tumor", "malignant islet cell tumor", "Malignant Islet cell tumor", "Malignant Islet cell tumour", "Islet Cell Tumor, Malignant", "pancreatic endocrine cancer", "endocrine pancreatic cancer", "endocrine pancreas carcinoma", "Endocrine pancreatic carcinoma", "Pancreatic Endocrine Carcinoma", "pancreas; islet cell carcinoma", "pancreatic endocrine carcinoma", "Carcinoma of endocrine pancreas", "carcinoma; islet cell, pancreas", "pancreas; carcinoma, islet cell", "carcinoma of endocrine pancreas", "Pancreatic islet cell carcinoma", "islet cell; carcinoma, pancreas", "Pancreatic Neuroendocrine Cancer", "islet cell carcinoma (diagnosis)", "cancer of the endocrine pancreas", "carcinoma, islet cell, malignant", "Pancreatic Neuroendocrine cancer", "islet cell carcinoma of pancreas", "CARCINOMA, ISLET CELL, MALIGNANT", "Malignant pancreatic islet neoplasm", "carcinoma of the endocrine pancreas", "pancreatic neuroendocrine carcinoma", "Pancreatic Neuroendocrine Carcinoma", "malignant pancreatic endocrine tumor", "Malignant Pancreatic Endocrine Tumor", "poorly-differentiated pancreatic NEN", "neuroendocrine carcinoma of pancreas", "poorly-differentiated NEN of pancreas", "Pancreatic endocrine tumor, malignant", "Pancreatic endocrine tumour, malignant", "carcinoma; islet cell, unspecified site", "Malignant tumor of Islets of Langerhans", "islet cell; carcinoma, unspecified site", "Malignant tumour of Islets of Langerhans", "malignant neoplasm of islets of Langerhans", "malignant neoplasm of Islets of Langerhans", "Malignant neoplasm of islets of langerhans", "Malignant neoplasm of Islets of Langerhans", "Carcinoma of endocrine pancreas (disorder)", "Malignant neoplasm of islets of Langerhans", "Carcinoma of endocrine pancreas (diagnosis)", "Pancreatic islet cell neoplasm malignant NOS", "islet cell carcinoma of pancreas (diagnosis)", "Poorly Differentiated Neuroendocrine Neoplasm", "Islet cell carcinoma (morphologic abnormality)", "High-Grade Pancreatic Neuroendocrine Carcinoma", "High Grade Pancreatic Neuroendocrine Carcinoma", "high grade pancreatic neuroendocrine carcinoma", "high-grade pancreatic neuroendocrine carcinoma", "islet cell carcinoma (morphologic abnormality)", "Malignant tumor of Islets of Langerhans (disorder)", "Poorly Differentiated Pancreatic Endocrine Carcinoma", "poorly differentiated pancreatic endocrine carcinoma", "malignant neoplasm of Islets of Langerhans (diagnosis)", "poorly-differentiated pancreatic neuroendocrine neoplasm", "poorly-differentiated neuroendocrine neoplasm of pancreas", "pancreatic neoplasm malignant carcinoma endocrine pancreas", "Malignant neoplasm of Islets of Langerhans, any part of pancreas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic endocrine carcinoma", "shortest_name_length": 6}
{"curie": "MONDO:0013262", "names": ["LVNC5", "CMD1S", "dilated cardiomyopathy-1S", "dilated cardiomyopathy 1S", "cardiomyopathy, dilated, 1S", "CARDIOMYOPATHY, DILATED, 1S", "Cardiomyopathy, Dilated, 1s", "dilated cardiomyopathy type 1S", "left ventricular noncompaction 5", "cardiomyopathy, dilated, type 1S", "LEFT VENTRICULAR NONCOMPACTION 5", "MYH7 familial isolated dilated cardiomyopathy", "familial isolated dilated cardiomyopathy caused by mutation in MYH7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1S", "shortest_name_length": 5}
{"curie": "UMLS:C5237208", "names": ["Skin Carcinosarcoma", "Skin Metaplastic Carcinoma", "Skin Sarcomatoid Squamous Cell Carcinoma", "Skin Pseudosarcomatous Squamous Cell Carcinoma", "Skin Squamous Cell Carcinoma with Sarcomatoid Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin Squamous Cell Carcinoma with Sarcomatoid Differentiation", "shortest_name_length": 19}
{"curie": "UMLS:C1610069", "names": ["Circulatory depression"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Circulatory depression", "shortest_name_length": 22}
{"curie": "MONDO:0016096", "names": ["Ovarian nondysgerm. GCT, NOS", "ovarian Nondysgerminomatous germ cell tumor", "Ovarian Nondysgerminomatous Germ Cell Tumor", "Ovarian Non-Dysgerminomatous Germ Cell Tumor", "ovarian non-dysgerminomatous germ cell tumor", "non-dysgerminomatous germ cell cancer of ovary", "Ovarian nondysgerminomatous germ cell tumor, NOS", "malignant non-dysgerminomatous germ cell tumor of ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant non-dysgerminomatous germ cell tumor of ovary", "shortest_name_length": 28}
{"curie": "UMLS:C1336860", "names": ["Undifferentiated Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Undifferentiated Malignant Neoplasm", "shortest_name_length": 35}
{"curie": "MONDO:0009441", "names": ["LI1", "ICR2", "ARCI1", "LI1, FORMERLY", "Collodion Fetus", "COLLODION FETUS", "collodion fetus", "Fetus, Collodion", "Newborn Desquamation", "ichthyosis congenita", "Ichthyosis, Lamellar", "ichthyosis lamellar 1", "Newborn Desquamations", "ichthyosis congenita 2", "Ichthyosis Congenita I", "Desquamation of Newborn", "Ichthyosis Congenita II", "Collodion Baby Syndrome", "ICHTHYOSIS CONGENITA II", "desquamation of newborn", "bathing suit ichthyosis", "DESQUAMATION OF NEWBORN", "ichthyosis, lamellar, 1", "Ichthyosis, Lamellar, 1", "Ichthyosis Congenita IIs", "Collodion Baby Syndromes", "Syndrome, Collodion Baby", "Congenita II, Ichthyosis", "Baby Syndrome, Collodion", "Congenita IIs, Ichthyosis", "Baby Syndromes, Collodion", "Syndromes, Collodion Baby", "lamellar ichthyosis, type 1", "Lamellar Ichthyosis, Type 1", "collodion baby, self-healing", "lamellar exfoliation of newborn", "ichthyosis, lamellar, 1, formerly", "ICHTHYOSIS, LAMELLAR, 1, FORMERLY", "autosomal recessive congenital ichthyosis 1", "ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 1", "ichthyosis, congenital, autosomal recessive 1", "autosomal recessive congenital ichthyosis type 1", "ichthyosis, congenital, autosomal recessive type 1", "ichthyosis, congenital, autosomal recessive 1, with bathing suit distribution", "ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 1, WITH BATHING SUIT DISTRIBUTION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive congenital ichthyosis 1", "shortest_name_length": 3}
{"curie": "UMLS:C4744721", "names": ["High Risk Chronic Myelomonocytic Leukemia", "High-Risk Chronic Myelomonocytic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Risk Chronic Myelomonocytic Leukemia", "shortest_name_length": 41}
{"curie": "MONDO:0017998", "names": ["PLAN", "PLA2G6-associated neurodegeneration", "PLA2G6 neurodegeneration with brain iron accumulation", "neurodegeneration with brain iron accumulation caused by mutation in PLA2G6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PLA2G6-associated neurodegeneration", "shortest_name_length": 4}
{"curie": "UMLS:C0018598", "names": ["Harding-Passey Melanoma", "Harding Passey Melanoma", "Melanoma, Harding Passey", "Melanoma, Harding-Passey", "Harding-Passey Malignant Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Melanoma, Harding-Passey", "shortest_name_length": 23}
{"curie": "MONDO:0019809", "names": ["Congenital aortic insufficiency", "congenital aortic insufficiency", "Congenital Aortic Insufficiency", "Congenital aortic regurgitation", "congenital aortic regurgitation", "aortic regurgitation congenital", "Aortic regurgitation, congenital", "AR - Congenital aortic regurgitation", "Congenital aortic valve incompetence", "Congenital Aortic Valve Insufficiency", "Congential aortic valve insufficiency", "Congential Aortic Valve Insufficiency", "congenital aortic valve insufficiency", "deformity; aortic valve, insufficiency", "aortic valve; deformity, insufficiency", "aortic valve; insufficiency, congenital", "Congenital insufficiency of aortic valve", "Congenital Insufficiency of Aortic Valve", "congenital insufficiency of aortic valve", "insufficiency; aorta (valve), congenital", "congenital aortic regurgitation (diagnosis)", "Congenital bicuspid aortic valve insufficiency", "Congenital insufficiency of aortic valve (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital aortic valve insufficiency", "shortest_name_length": 31}
{"curie": "UMLS:C5420076", "names": ["Sinonasal Plasmacytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Plasmacytoma", "shortest_name_length": 22}
{"curie": "UMLS:C1708181", "names": ["Gallbladder Pyloric Gland Adenoma", "Gallbladder Tubulopapillary Adenoma", "tubulopapillary adenoma of gallbladder", "tubulopapillary adenoma of gallbladder (diagnosis)", "Intracholecystic Papillary Tubular Neoplasm, Gastric Pyloric, Simple Mucinous Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tubulopapillary adenoma of gallbladder", "shortest_name_length": 33}
{"curie": "MONDO:0001173", "names": ["Acute Salpingitis", "acute salpingitis", "salpingitis acute", "Salpingitis;acute", "Acute salpingitis", "salpingitis; acute", "acute; salpingitis", "SALPINGITIS, ACUTE", "salpingitis, acute", "Salpingitis acute NOS", "Acute salpingitis (disorder)", "acute salpingitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute salpingitis", "shortest_name_length": 17}
{"curie": "UMLS:C0037358", "names": ["Modified Smallpox", "Modified smallpox", "Smallpox, modified", "Modified smallpox (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Modified smallpox", "shortest_name_length": 17}
{"curie": "MONDO:0017189", "names": ["NIPHS", "NI-PHH", "Non-insulinoma pancreatogenous hypoglycemia syndrome", "adult-onset non-insulinoma persistent hyperinsulinemic hypoglycemia", "Adult onset non-insulinoma persistent hyperinsulinemic hypoglycemia", "Adult onset non-insulinoma persistent hyperinsulinaemic hypoglycaemia", "Adult onset non-insulinoma persistent hyperinsulinemic hypoglycemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult-onset non-insulinoma persistent hyperinsulinemic hypoglycemia", "shortest_name_length": 5}
{"curie": "UMLS:C1699737", "names": ["Intraoperative respiratory injury", "Intraoperative Respiratory Injury", "intraoperative respiratory injury", "intraoperative respiratory injury (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraoperative Respiratory Injury", "shortest_name_length": 33}
{"curie": "MONDO:0100390", "names": ["AML, der12p", "AML, der(12p)", "acute myeloid leukemia, der12p"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, der12p", "shortest_name_length": 11}
{"curie": "MONDO:0012802", "names": ["OCACS", "Oculoauricular Syndrome", "OCULOAURICULAR SYNDROME", "oculoauricular syndrome", "oculoauricular syndrome, Schorderet type", "SCHORDERET-MUNIER-FRANCESCHETTI SYNDROME", "Schorderet-Munier-Franceschetti syndrome", "MICROPHTHALMIA, MICROCORNEA, ANTERIOR SEGMENT DYSGENESIS, CATARACT, OCULAR COLOBOMA, RETINAL PIGMENT EPITHELIUM ABNORMALITIES, ROD-CONE DYSTROPHY, AND ANOMALIES OF THE EXTERNAL EAR", "microphthalmia, microcornea, anterior segment dysgenesis, cataract, ocular coloboma, retinal pigment epithelium abnormalities, Rod-cone dystrophy, and anomalies of the external Ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculoauricular syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0012936", "names": ["Clls5", "CLLS5", "leukemia, chronic lymphocytic susceptibility to, 5", "leukemia, chronic lymphocytic, susceptibility to, 5", "LEUKEMIA, CHRONIC LYMPHOCYTIC, SUSCEPTIBILITY TO, 5", "leukemia, chronic lymphocytic, susceptibility to, type 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukemia, chronic lymphocytic, susceptibility to, 5", "shortest_name_length": 5}
{"curie": "MONDO:0005606", "names": ["tubular carcinoma", "Tubular carcinoma", "carcinoma tubular", "Tubular Carcinoma", "tubular carcinomas", "Carcinoma, Tubular", "Tubular Carcinomas", "Carcinomas, Tubular", "Tubular Adenocarcinoma", "Tubular adenocarcinoma", "tubular adenocarcinoma", "Adenocarcinoma, Tubular", "Tubular Adenocarcinomas", "Adenocarcinomas, Tubular", "carcinoma, tubular cell, malignant", "tubular adenocarcinoma (diagnosis)", "CARCINOMA, TUBULAR CELL, MALIGNANT", "tubular adenocarcinoma (morphologic abnormality)", "Tubular adenocarcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tubular adenocarcinoma", "shortest_name_length": 17}
{"curie": "MONDO:0034054", "names": ["LPFS3", "CD70 Deficiency", "CD70 DEFICIENCY", "CID due to CD70 deficiency", "lymphoproliferative syndrome 3", "LYMPHOPROLIFERATIVE SYNDROME 3", "Combined immunodeficiency due to CD70 deficiency", "severe combined immunodeficiency due to CD70 deficiency", "Combined immunodeficiency due to CD70 deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe combined immunodeficiency due to CD70 deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C1706726", "names": ["Adrenal Gland Adenomatoid Tumor", "Adrenal Cortex Adenomatoid Tumor", "Adrenal Cortical Adenomatoid Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adrenal Cortical Adenomatoid Tumor", "shortest_name_length": 31}
{"curie": "MONDO:0001698", "names": ["Tinea profunda", "tinea profunda", "granuloma majocchi", "majocchi granuloma", "Majocchi granuloma", "Majocchi; granuloma", "granuloma; Majocchi", "granuloma majocchi's", "Majocchi's granuloma", "majocchi's granuloma", "Trichophytic granuloma", "trichophytic granuloma", "Granuloma trichophyticum", "granuloma trichophyticum", "Tinea profunda (disorder)", "Tinea profunda (diagnosis)", "deep seated dermatophytosis", "Deep seated dermatophytosis", "dermatophytosis tinea profunda"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tinea profunda", "shortest_name_length": 14}
{"curie": "MONDO:0013681", "names": ["BASD4", "AMACR", "AMACRD", "AMACR deficiency", "AMACR DEFICIENCY", "2-methylacyl-CoA racemase deficiency", "alpha-methylacyl-CoA racemase deficiency", "Alpha-Methylacyl-CoA Racemase Deficiency", "ALPHA-METHYLACYL-CoA RACEMASE DEFICIENCY", "Alpha-methylacyl-CoA racemase deficiency", "Alpha-methyl-acyl-CoA racemase deficiency", "Congenital bile acid synthesis defect type 4", "Alpha-methylacyl-CoA racemase deficiency disorder", "Alpha-methylacyl-CoA racemase deficiency disorder (disorder)", "Liver disease-retinitis pigmentosa-polyneuropathy-epilepsy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alpha-methylacyl-CoA racemase deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0013489", "names": ["DFNB89", "autosomal recessive deafness 89", "DEAFNESS, AUTOSOMAL RECESSIVE 89", "deafness, autosomal recessive 89", "deafness, autosomal recessive type 89", "autosomal recessive nonsyndromic deafness 89", "KARS autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 89", "autosomal recessive nonsyndromic deafness type 89", "autosomal recessive nonsyndromic deafness caused by mutation in KARS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 89", "shortest_name_length": 6}
{"curie": "UMLS:C0278961", "names": ["Arrhythmia Requiring Therapy", "arrhythmias requiring therapy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arrhythmia Requiring Therapy", "shortest_name_length": 28}
{"curie": "MONDO:0001898", "names": ["choroidopathy", "Choroid disease", "Choroid Disease", "choroid disease", "choroid disorder", "Disease, Choroid", "Choroid Diseases", "Choroid Disorder", "choroid; disorder", "Diseases, Choroid", "Choroidal Disease", "Choroid--Diseases", "Disease, Choroidal", "Choroidal Diseases", "Diseases, Choroidal", "optic choroid disease", "optic choroid disorder", "disease of optic choroid", "disorder of optic choroid", "Disorder of choroid of eye", "Abnormality of the choroid", "Abnormal choroid morphology", "choroid disorder (diagnosis)", "disease (or disorder); choroid", "Unspecified disorder of choroid", "Disorder of choroid, unspecified", "optic choroid disease or disorder", "disease or disorder of optic choroid", "Disorder of choroid of eye (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "optic choroid disorder", "shortest_name_length": 13}
{"curie": "MONDO:0017078", "names": ["craniocele", "Craniocele", "Cephalocele", "cephalocele", "Cranioceles", "Bifid skull", "Cephaloceles", "Encephalocele", "CRANIOSCHISIS", "Bifid Cranium", "cranioschisis", "ENCEPHALOCELE", "encephalocele", "Cranioschises", "Cranioschisis", "Cranium, Bifid", "encephaloceles", "Bifid Craniums", "Hernia cerebri", "Encephaloceles", "cranium bifidum", "cerebral hernia", "Cranium Bifidum", "Craniums, Bifid", "Cerebral Hernia", "Cranium bifidum", "Cerebral Hernias", "Bifidum, Cranium", "Cranium Bifidums", "Hernia, Cerebral", "Hernias, Cerebral", "Bifidums, Cranium", "Encephalocele, NOS", "cephalocele (disease)", "Cranioschisis (disorder)", "Encephalocele (disorder)", "encephalocele (diagnosis)", "Encephalocele, unspecified", "Congenital cerebral hernia", "Cranial Meningoencephalocele", "Cranial Meningoencephaloceles", "Meningoencephalocele, Cranial", "Meningoencephaloceles, Cranial", "Congenital cerebral hernia (disorder)", "Congenital cerebral hernia (diagnosis)", "congenital malformation cerebral hernia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cephalocele", "shortest_name_length": 10}
{"curie": "MONDO:0021211", "names": ["BRAIN TUMOR", "Brain Tumor", "Brain tumor", "brain tumor", "brain tumour", "Brain tumour", "Brain tumors", "brain cancer", "Brain Tumors", "brain tumors", "Tumor, Brain", "Brain--Tumors", "brain tumours", "BRAIN NEOPLASM", "tumor of brain", "Brain Neoplasm", "brain neoplasm", "Tumor of Brain", "Brain neoplasm", "Brain Neoplasms", "Neoplasm, Brain", "Brain tumor NOS", "brain neoplasms", "Brain tumour NOS", "BT - Brain tumor", "Neoplasms, Brain", "Neoplasm of brain", "neoplasm of brain", "BT - Brain tumour", "Neoplasm of Brain", "Intracranial tumor", "intracranial tumor", "INTRACRANIAL TUMOR", "Brain neoplasm NOS", "Tumor of the Brain", "Intracranial Tumor", "tumor of the Brain", "Intracranial tumors", "Intracranial tumour", "intracranial tumors", "intracranial tumours", "neoplasm of the brain", "Intracranial Neoplasm", "intracranial neoplasm", "Intracranial neoplasm", "Neoplasm of the Brain", "Intracranial Neoplasms", "Neoplasm, Intracranial", "Neoplasms, Intracranial", "brain tumor (diagnosis)", "brain neoplasm (disease)", "ICT - Intracranial tumor", "ICT - Intracranial tumour", "Neoplasm of brain (disorder)", "neoplasm of head intracranial", "neoplasm of brain (diagnosis)", "Intracranial tumor (disorder)", "Intracranial neoplasm (diagnosis)", "Neoplasm of unspecified nature of brain", "Intracranial Central Nervous System Tumor", "Intracranial Central Nervous System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brain neoplasm", "shortest_name_length": 11}
{"curie": "UMLS:C4744400", "names": ["Recurrent Endometrial Mixed Cell Adenocarcinoma", "Recurrent Endometrial Mixed Epithelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Endometrial Mixed Cell Adenocarcinoma", "shortest_name_length": 47}
{"curie": "UMLS:C1336278", "names": ["Stage III Uveal Melanoma", "Stage III Melanoma of Uvea", "Stage III Melanoma of the Uvea", "Stage III Uveal Melanoma AJCC v7", "Stage III Uveal Malignant Melanoma", "Stage III Malignant Melanoma of Uvea", "Stage III Malignant Melanoma of the Uvea"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Uveal Melanoma AJCC v7", "shortest_name_length": 24}
{"curie": "MONDO:0005630", "names": ["Actinobacilloses", "Actinobacillosis", "actinobacillosis", "Actinobacillosis, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "actinobacillosis", "shortest_name_length": 16}
{"curie": "UMLS:C4048329", "names": ["Immunosuppression"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immunosuppression", "shortest_name_length": 17}
{"curie": "MONDO:0004055", "names": ["acute inflammation of lacrimal passage", "Acute inflammation of lacrimal passages", "acute inflammation of lacrimal passages", "inflammation of lacrimal passages acute", "Acute inflammation of lacrimal passages (disorder)", "acute inflammation of lacrimal passages (diagnosis)", "Acute and unspecified inflammation of lacrimal passages"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute inflammation of lacrimal passage", "shortest_name_length": 38}
{"curie": "MONDO:0019984", "names": ["renal tubular dysgenesis due to twin-twin transfusion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal tubular dysgenesis due to twin-twin transfusion", "shortest_name_length": 53}
{"curie": "MONDO:0012881", "names": ["MAFD7", "BIPOLAR AFFECTIVE DISORDER", "bipolar affective disorder", "Major Affective Disorder 7", "MAJOR AFFECTIVE DISORDER 7", "major affective disorder 7", "major affective disorder type 7", "major affective disorder-7, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "major affective disorder 7", "shortest_name_length": 5}
{"curie": "MONDO:0054677", "names": ["COXPD33", "combined oxidative phosphorylation deficiency 33", "Combined Oxidative Phosphorylation Deficiency 33", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 33"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation deficiency 33", "shortest_name_length": 7}
{"curie": "MONDO:0022898", "names": ["craniosynostosis intellectual disability heart defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniosynostosis intellectual disability heart defects", "shortest_name_length": 54}
{"curie": "UMLS:C0751415", "names": ["Atherosclerotic Parkinsonism", "Parkinsonism, Atherosclerotic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atherosclerotic Parkinsonism", "shortest_name_length": 28}
{"curie": "UMLS:C4744449", "names": ["Metastatic Malignant Neoplasm in the Thorax", "Metastatic Malignant Neoplasm in the Thoracic Cavity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Malignant Neoplasm in the Thoracic Cavity", "shortest_name_length": 43}
{"curie": "UMLS:C1333810", "names": ["Genital Human Papillomavirus Infection", "Genital Human Papilloma Virus Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Genital Human Papillomavirus Infection", "shortest_name_length": 38}
{"curie": "UMLS:C3897506", "names": ["Stage IVC Thyroid Gland Papillary Cancer", "Stage IVC Thyroid Gland Papillary Carcinoma", "Stage IVC Thyroid Gland Papillary Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Thyroid Gland Papillary Carcinoma AJCC v7", "shortest_name_length": 40}
{"curie": "UMLS:C1334006", "names": ["High Grade Breast Mucoepidermoid Carcinoma", "High Grade Mucoepidermoid Breast Carcinoma", "High-Grade Mucoepidermoid Carcinoma of Breast", "High-Grade Mucoepidermoid Carcinoma of the Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Breast Mucoepidermoid Carcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0015640", "names": ["Benign infantile seizure with mild gastroenteritis syndrome", "Benign infantile seizures associated with mild gastroenteritis", "benign infantile seizures associated with mild gastroenteritis", "Benign infantile seizure with mild gastroenteritis syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign infantile seizures associated with mild gastroenteritis", "shortest_name_length": 59}
{"curie": "UMLS:C0268733", "names": ["Acute nephritis", "acute nephritis", "Nephritis acute", "NEPHRITIS ACUTE", "nephritis; acute", "acute; nephritis", "Acute nephritis, NOS", "Acute nephritic syndrome", "acute nephritic syndrome", "NEPHRITIC SYNDROME, ACUTE", "acute; nephritic syndrome", "syndrome; nephritic, acute", "nephritic; syndrome, acute", "Acute nephritis (disorder)", "acute nephritis (diagnosis)", "Nephritis specified as acute", "acute nephritic syndrome (diagnosis)", "Acute nephritic syndrome, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute nephritis", "shortest_name_length": 15}
{"curie": "UMLS:C4086177", "names": ["Childhood Medullary Thyroid Carcinoma", "Childhood Thyroid Gland Medullary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Thyroid Gland Medullary Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0016481", "names": ["silver-Russell syndrome due to 11p15 microduplication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "silver-Russell syndrome due to 11p15 microduplication", "shortest_name_length": 53}
{"curie": "UMLS:C0277355", "names": ["fleas", "Siphonapterosis", "Flea Infestation", "flea infestation", "Flea infestation", "Flea Infestations", "Infestation, Flea", "Infestations, Flea", "Infestation by fleas", "Infestation (by);fleas", "Dermatosis due to flea", "Infestation by fleas, NOS", "Dermatosis caused by flea", "Infestation by Siphonaptera", "Infestation by Siphonaptera, NOS", "Dermatosis caused by flea (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Flea Infestation", "shortest_name_length": 5}
{"curie": "MONDO:0008606", "names": ["Say Field Coldwell syndrome", "Say-field-Coldwell syndrome", "TRIPHALANGEAL THUMBS AND DISLOCATION OF PATELLA", "Triphalangeal thumbs and dislocation of patella", "triphalangeal thumbs and dislocation of patella", "triphalangeal thumbs-dislocation of patella syndrome", "Triphalangeal thumb and dislocation of patella syndrome", "Triphalangeal thumb and dislocation of patella syndrome (disorder)", "polydactyly with triphalangeal thumbs, brachydactyly, camptodactyly, congenital dislocation of the patellas, short stature and borderline intelligence"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Say-field-Coldwell syndrome", "shortest_name_length": 27}
{"curie": "MONDO:0019490", "names": ["PFHB", "familial PCCD", "familial Lev disease", "familial Lenegre disease", "familial Lenègre disease", "familial Lev-Lenegre disease", "familial Lev-Lenègre disease", "hereditary bundle branch defect", "progressive familial heart block", "familial progressive heart block", "familial progressive cardiac conduction defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive familial heart block", "shortest_name_length": 4}
{"curie": "UMLS:C0854944", "names": ["Stage IV Ovarian Choriocarcinoma", "Stage IV Ovarian Choriocarcinoma AJCC v6", "Stage IV Ovarian Choriocarcinoma AJCC v7", "Ovarian germ cell choriocarcinoma stage IV", "Ovarian Germ Cell Choriocarcinoma Stage IV", "Stage IV Ovarian Germ Cell Choriocarcinoma", "Ovarian Germ Cell Choriocarcinoma, Stage IV"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian germ cell choriocarcinoma stage IV", "shortest_name_length": 32}
{"curie": "UMLS:C5554630", "names": ["Refractory Low Grade Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Low Grade Astrocytoma", "shortest_name_length": 32}
{"curie": "MONDO:0005535", "names": ["oral Crohn disease", "Oral Crohn's disease", "oral Crohn's disease", "Orofacial Crohn's disease", "Crohn's disease of oral soft tissues", "Orofacial Crohn's disease (diagnosis)", "Crohn's disease of oral soft tissues (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oral Crohn disease", "shortest_name_length": 18}
{"curie": "MONDO:0700057", "names": ["neurologic pain syndrome", "neurological pain disease", "neurological pain disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurological pain disorder", "shortest_name_length": 24}
{"curie": "UMLS:C1711168", "names": ["Mediastinal T Acute Lymphoblastic Leukemia", "Mediastinal T-Acute Lymphoblastic Leukemia", "Mediastinal Precursor T-Lymphoblastic Leukemia", "Mediastinal T-Cell Acute Lymphoblastic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mediastinal T Acute Lymphoblastic Leukemia", "shortest_name_length": 42}
{"curie": "MONDO:0007011", "names": ["Heerfordt", "uveoparotitis", "Uveoparotitis", "Uveoparotitides", "Uveoparotid fever", "Uveoparotid Fever", "uveoparotid fever", "fever; uveoparotid", "heerfordt syndrome", "Heerfordt Syndrome", "Fever, Uveoparotid", "Uveoparotid Fevers", "uveoparotid; fever", "Heerfordt syndrome", "febris; uveoparotid", "heerfordts syndrome", "Fevers, Uveoparotid", "uveoparotid; febris", "Syndrome, Heerfordt", "heerfordt's syndrome", "Heerfordt's syndrome", "Uveoparotid fever syndrome", "uveoparotid fever (diagnosis)", "Uveoparotid fever [Heerfordt]", "Heerfordt-Waldenstrom syndrome", "Heerfordt-Waldenström syndrome", "Heerfordt's syndrome (disorder)", "Heerfordt-Waldenstroem syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uveoparotid fever", "shortest_name_length": 9}
{"curie": "MONDO:0013706", "names": ["MRT23", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 23", "mental retardation, autosomal recessive 23", "intellectual disability, autosomal recessive 23", "autosomal recessive intellectual developmental disorder 23", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 23"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 23", "shortest_name_length": 5}
{"curie": "MONDO:0024358", "names": ["CompSAS", "mixed sleep apnea", "Mixed Sleep Apnea", "Mixed sleep apnea", "Mixed Sleep Apneas", "Sleep Apnea, Mixed", "Mixed sleep apnoea", "complex sleep apnea", "Complex sleep apnea", "Sleep Apneas, Mixed", "Complex sleep apnoea", "Mixed sleep apnea (disorder)", "Mixed Central and Obstructive Sleep Apnea", "Sleep Apnea, Mixed Central and Obstructive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complex sleep apnea", "shortest_name_length": 7}
{"curie": "UMLS:C4687710", "names": ["Refractory Medulloblastoma, SHH-Activated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Medulloblastoma, SHH-Activated", "shortest_name_length": 41}
{"curie": "MONDO:0022900", "names": ["cretinism athyreotic", "athyreotic congenital hypothyroidism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "athyreotic congenital hypothyroidism", "shortest_name_length": 20}
{"curie": "UMLS:C1142011", "names": ["Orchitis noninfective"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Orchitis noninfective", "shortest_name_length": 21}
{"curie": "UMLS:C2981391", "names": ["Stage IVA Appendix Cancer", "Stage IVA Appendix Carcinoma", "Stage IVA Appendix Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Appendix Carcinoma AJCC v7", "shortest_name_length": 25}
{"curie": "MONDO:0024503", "names": ["GEP NET", "GEP-NET", "GEP-NEN", "GEP tumors", "carcinoid tumor", "digestive system NET", "Gastrointestinal NET", "Digestive System NET", "GEP neuroendocrine tumor", "Gastroenteropancreatic NET", "carcinoid tumor of digestive system", "Digestive System Neuroendocrine Tumor", "Gastrointestinal Neuroendocrine Tumor", "digestive system neuroendocrine tumor", "gastroenteropancreatic endocrine tumor", "gastrointestinal neuroendocrine neoplasm", "Gastrointestinal Neuroendocrine Neoplasm", "Digestive System Neuroendocrine Neoplasm", "digestive system neuroendocrine neoplasm", "gastroenteropancreatic neuroendocrine tumor", "neuroendocrine neoplasm of digestive system", "Gastroenteropancreatic Neuroendocrine Tumor", "Gastroenteropancreatic neuroendocrine tumor", "Gastro-enteropancreatic neuroendocrine tumor", "gastro-enteropancreatic neuroendocrine tumor", "gastrointestinal neuroendocrine benign tumor", "Gastrointestinal System Neuroendocrine Tumor", "alimentary part of gastrointestinal system NET", "Gastroenteropancreatic neuroendocrine neoplasm", "Gastroenteropancreatic Neuroendocrine Neoplasm", "gastroenteropancreatic neuroendocrine neoplasm", "Gastrointestinal System Neuroendocrine Neoplasm", "gastrointestinal system neuroendocrine neoplasm", "Digestive System Well Differentiated Neuroendocrine Tumor", "alimentary part of gastrointestinal system neuroendocrine tumor", "alimentary part of gastrointestinal system neuroendocrine neoplasm", "neuroendocrine neoplasm of alimentary part of gastrointestinal system", "digestive system neuroendocrine tumor, well differentiated, low or intermediate grade", "alimentary part of gastrointestinal system neuroendocrine tumor, well differentiated, low or intermediate grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "digestive system neuroendocrine neoplasm", "shortest_name_length": 7}
{"curie": "UMLS:C1332967", "names": ["Childhood DLBCL", "Diffuse Large B-Cell Lymphoma", "Pediatric Diffuse Large B Cell Lymphoma", "Childhood Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Diffuse Large B-Cell Lymphoma", "shortest_name_length": 15}
{"curie": "UMLS:C0151923", "names": ["STENOSIS JEJUNUM", "Jejunal stenosis", "Jejunal Stenosis", "Stenosis jejunum", "jejunum; stenosis", "stenosis; jejunum", "STENOSIS OF JEJUNUM", "stenosis of jejunum", "Stenosis of jejunum", "Stenosis of jejunum (disorder)", "stenosis of jejunum (diagnosis)", "stenosis of small intestine jejunum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jejunal Stenosis", "shortest_name_length": 16}
{"curie": "MONDO:0043358", "names": ["engraftment syndrome", "Engraftment syndrome", "Engraftment Syndrome", "Engraftment syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "engraftment syndrome", "shortest_name_length": 20}
{"curie": "MONDO:0014024", "names": ["SPG43", "hereditary spastic paraplegia 43", "hereditary spastic paraplegia type 43", "autosomal recessive spastic paraplegia 43", "SPASTIC PARAPLEGIA 43, AUTOSOMAL RECESSIVE", "spastic paraplegia 43, autosomal recessive", "Autosomal recessive spastic paraplegia type 43", "autosomal recessive spastic paraplegia type 43", "C19orf12 autosomal recessive complex spastic paraplegia", "familial spastic paraplegia autosomal recessive type 43", "Autosomal recessive spastic paraplegia type 43 (disorder)", "Autosomal recessive spastic paraplegia type 43 (diagnosis)", "autosomal recessive complex spastic paraplegia caused by mutation in C19orf12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 43", "shortest_name_length": 5}
{"curie": "UMLS:C1334776", "names": ["Soft Tissue Tumor of Uncertain Differentiation", "Soft Tissue Neoplasm of Uncertain Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Soft Tissue Tumor of Uncertain Differentiation", "shortest_name_length": 46}
{"curie": "MONDO:0013655", "names": ["MRD8", "NDHMSD", "MRD8, FORMERLY", "autosomal dominant mental retardation 8", "mental retardation, autosomal dominant 8", "autosomal dominant intellectual disability 8", "mental retardation, autosomal dominant type 8", "intellectual disability, autosomal dominant 8", "intellectual disability, autosomal dominant type 8", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 8, FORMERLY", "mental retardation, autosomal dominant 8, formerly", "intellectual disability, autosomal dominant 8, formerly", "autosomal dominant intellectual developmental disorder 8", "autosomal dominant non-syndromic intellectual disability 8", "GRIN1 autosomal dominant non-syndromic intellectual disability", "autosomal dominant non-syndromic intellectual disability caused by mutation in GRIN1", "neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant", "NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 8", "shortest_name_length": 4}
{"curie": "MONDO:0002776", "names": ["Preauricular cyst", "preauricular cyst", "external ear disease", "external ear disorder", "External ear disorder", "External Ear Disorder", "Ear, External--Diseases", "disease of external ear", "Diseases of external ear", "Disorder of external ear", "disorder of external ear", "Disorders of external ear", "External ear disorder NOS", "preauricular cyst (disorder)", "DISORDERS OF THE EXTERNAL EAR", "Preauricular sinus or fistula", "Disorder of external ear, NOS", "preauricular sinus or fistula", "preauricular sinus and fistula", "Preauricular sinus and fistula", "external ear disease or disorder", "Diseases of external ear (H60-H62)", "Disorder of external ear (disorder)", "disease or disorder of external ear", "disease (or disorder); external, ear", "disorder of external ear (diagnosis)", "Unspecified disorder of external ear", "disease (or disorder); ear, external", "Disorder of external ear, unspecified", "preauricular sinus and fistula (disorder)", "preauricular sinus or fistula NOS (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "external ear disorder", "shortest_name_length": 17}
{"curie": "MONDO:0002931", "names": ["Conjunctivochalasis", "conjunctivochalasis", "Conjunctivochalasis (disorder)", "conjunctivochalasis (diagnosis)", "Chronic localised conjunctival chemosis", "Chronic localized conjunctival chemosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "conjunctivochalasis", "shortest_name_length": 19}
{"curie": "MONDO:0030527", "names": ["EBS2C", "EPIDERMOLYSIS BULLOSA SIMPLEX 2C, LOCALIZED", "epidermolysis bullosa simplex 2C, localized", "EPIDERMOLYSIS BULLOSA SIMPLEX 2C, WEBER-COCKAYNE TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolysis bullosa simplex 2C, localized", "shortest_name_length": 5}
{"curie": "MONDO:0006585", "names": ["lichen simplex", "Lichen simplex", "lichen; simplex", "neurodermatitis", "Neurodermatitis", "simplex; lichen", "lichens simplex", "NEURODERMATITIS", "Neurodermatitides", "Lichenified eczema", "eczema; lichenified", "lichenified; eczema", "Lichenoid dermatitis", "Local neurodermatitis", "Neurodermatitis, local", "lichen simplex chronic", "LICHEN SIMPLEX, CHRONIC", "Lichen simplex chronicus", "LICHEN SIMPLEX CHRONICUS", "lichen simplex chronicus", "chronicus lichen simplex", "Lichen Simplex Chronicus", "lichen simplex Chronicus", "Localized Neurodermatitis", "chronicus lichens simplex", "Neurodermatitis, Localized", "Neurodermatitis, localized", "DERMATITIS NEURODERMATITIS", "Localized Neurodermatitides", "neurodermatitis (diagnosis)", "Neurodermatitides, Localized", "Circumscribed neurodermatitis", "Neurodermatitis circumscripta", "Circumscribed Neurodermatitis", "neurodermatitis circumscripta", "LICHEN SIMPLEX CIRCUMSCRIPTUS", "NEURODERMATITIS, CIRCUMSCRIBED", "LSC - Lichen simplex chronicus", "Neurodermatitis, Circumscribed", "Circumscribed Neurodermatitides", "Neurodermatitides, Circumscribed", "Lichen simplex chronicus (disorder)", "lichen simplex chronicus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodermatitis", "shortest_name_length": 14}
{"curie": "UMLS:C3640035", "names": ["Lumbar Meningocele"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lumbar Meningocele", "shortest_name_length": 18}
{"curie": "MONDO:0013119", "names": ["DFNB77", "autosomal recessive deafness 77", "DEAFNESS, AUTOSOMAL RECESSIVE 77", "Deafness, Autosomal Recessive 77", "deafness, autosomal recessive 77", "deafness, autosomal recessive type 77", "DEAFNESS, AUTOSOMAL RECESSIVE 77 (disorder)", "autosomal recessive nonsyndromic deafness 77", "LOXHD1 autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 77", "autosomal recessive nonsyndromic deafness type 77", "autosomal recessive nonsyndromic deafness caused by mutation in LOXHD1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 77", "shortest_name_length": 6}
{"curie": "MONDO:0018822", "names": ["global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome", "shortest_name_length": 101}
{"curie": "UMLS:C4055188", "names": ["Congenital Neurogenic Bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Neurogenic Bladder", "shortest_name_length": 29}
{"curie": "MONDO:0022913", "names": ["cutler bass Romshe syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutler bass Romshe syndrome", "shortest_name_length": 27}
{"curie": "MONDO:0019186", "names": ["Q-fever", "Q fever", "q fever", "q-fever", "Q Fever", "fever q", "Q FEVER", "Q Fevers", "Fever, Q", "fever; Q", "Q; fever", "Fevers, Q", "Coxiellosis", "fever query", "query fever", "Query Fever", "Query fever", "Query Fevers", "Fever, Query", "BALKAN GRIPPE", "Fevers, Query", "Balkan grippe", "Abattoir fever", "nine Mile fever", "Nine Mile fever", "Nine-mile fever", "nine Mile; fever", "Balkan influenza", "FEVER, NINE MILE", "fever; nine Mile", "influenza; Balkan", "Q fever pneumonia", "Balkan; influenza", "Q fever (disorder)", "quadrilateral fever", "Quadrilateral fever", "Q-fever (diagnosis)", "quadrilateral; fever", "fever; quadrilateral", "DERRICK-BURNET DISEASE", "Coxiella burnetii fever", "Coxiella burnetii Fever", "Coxiella burnetii Fevers", "Fever, Coxiella burnetii", "Fevers, Coxiella burnetii", "Coxiella burnetii infection", "infection; Coxiella burnetii", "Coxiella burnetii; infection", "BRONCHOPNEUMONIA, HIBERNO-VERNAL", "Infection due to Coxiella burnetii", "infection due to Coxiella burnetii", "Coxiella burnetii infectious disease", "Coxiella burnetii disease or disorder", "Coxiella burnetii caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Q fever", "shortest_name_length": 7}
{"curie": "UMLS:C4683153", "names": ["Stage IIIC Posterior Uveal Melanoma AJCC v8", "Stage IIIC Choroidal and Ciliary Body Melanoma", "Stage IIIC Choroidal and Ciliary Body Melanoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Choroidal and Ciliary Body Melanoma AJCC v8", "shortest_name_length": 43}
{"curie": "UMLS:C1336180", "names": ["Stage IIB Esophagus Adenocarcinoma", "Stage IIB Esophageal Adenocarcinoma", "Stage IIB Adenocarcinoma of Esophagus", "Stage IIB Adenocarcinoma of the Esophagus", "Stage IIB Esophageal Adenocarcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Esophageal Adenocarcinoma AJCC v7", "shortest_name_length": 34}
{"curie": "MONDO:0002285", "names": ["pupil disease", "Pupil Disorder", "pupil disorder", "Pupil disorders", "Pupil Disorders", "disease of pupil", "Disorder of pupil", "disorder of pupil", "Pupillary Disorder", "Pupillary disorder", "PUPILLARY DISORDER", "pupillary disorder", "Pupillary Disorders", "Pupillary disorder NOS", "Pupillary disorder, NOS", "pupil disease or disorder", "disease or disorder of pupil", "Pupillary disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pupil disorder", "shortest_name_length": 13}
{"curie": "MONDO:0010813", "names": ["diabetes mellitus, insulin-dependent, neonatal", "PANCREATIC BETA CELL AGENESIS WITH NEONATAL DIABETES MELLITUS", "Pancreatic beta cell agenesis with neonatal diabetes mellitus", "pancreatic beta cell agenesis with neonatal diabetes mellitus", "Congenital absence of insulin-producing beta cells with diabetes mellitus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic beta cell agenesis with neonatal diabetes mellitus", "shortest_name_length": 46}
{"curie": "MONDO:0022786", "names": ["cleft palate colobomata radial synostosis deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleft palate colobomata radial synostosis deafness", "shortest_name_length": 50}
{"curie": "MONDO:0002313", "names": ["Spring ophthalmia", "spring; ophthalmia", "ophthalmia; spring", "Vernal Conjunctivitis", "vernal conjunctivitis", "Vernal conjunctivitis", "Spring conjunctivitis", "Conjunctivitis, Vernal", "CONJUNCTIVITIS, VERNAL", "Vernal Conjunctivitides", "Conjunctivitides, Vernal", "Vernal conjunctivitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vernal conjunctivitis", "shortest_name_length": 17}
{"curie": "MONDO:0014340", "names": ["ATFB15", "atrial fibrillation 15", "atrial fibrillation, familial, 15", "ATRIAL FIBRILLATION, FAMILIAL, 15", "NUP155 familial atrial fibrillation", "atrial fibrillation, familial, type 15", "familial atrial fibrillation caused by mutation in NUP155"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial fibrillation, familial, 15", "shortest_name_length": 6}
{"curie": "MONDO:0004109", "names": ["EPIGLOTTIS TUMOR", "Epiglottic tumor", "epiglottic tumor", "Epiglottis Tumor", "Epiglottis tumor", "Epiglottic Tumor", "epiglottis tumor", "tumor of epiglottis", "Tumor of Epiglottis", "epiglottic neoplasm", "epiglottis neoplasm", "Epiglottic neoplasm", "Epiglottic Neoplasm", "Epiglottis Neoplasm", "tumor of Epiglottis", "Neoplasm of epiglottis", "Neoplasm of Epiglottis", "neoplasm of Epiglottis", "neoplasm of epiglottis", "Tumor of the Epiglottis", "tumor of the Epiglottis", "Neoplasm of the Epiglottis", "neoplasm of the Epiglottis", "epiglottis neoplasm (disease)", "Neoplasm of epiglottis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epiglottis neoplasm", "shortest_name_length": 16}
{"curie": "UMLS:C1336314", "names": ["Stage II Renal Pelvis and Ureter Cancer", "Stage II Renal Pelvis and Ureter Carcinoma", "Stage II Renal Pelvis and Ureter Cancer AJCC v7", "Stage II Renal Pelvis and Ureter Carcinoma AJCC v7", "stage II transitional cell cancer of the renal pelvis and ureter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Renal Pelvis and Ureter Cancer AJCC v7", "shortest_name_length": 39}
{"curie": "UMLS:C4287893", "names": ["Gastroesophageal Junction Small Cell Carcinoma", "Gastroesophageal Junction Small Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastroesophageal Junction Small Cell Neuroendocrine Carcinoma", "shortest_name_length": 46}
{"curie": "MONDO:0034127", "names": ["iga pemphigus", "IgA pemphigus", "Immunoglobulin A pemphigus", "Immunoglobulin A pemphigus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IgA pemphigus", "shortest_name_length": 13}
{"curie": "MONDO:0015039", "names": ["lissencephaly with cerebellar hypoplasia type F", "Lissencephaly with cerebellar hypoplasia type F", "Lissencephaly co-occurrent with congenital cerebellar hypoplasia type F", "Lissencephaly co-occurrent with congenital cerebellar hypoplasia type F (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lissencephaly with cerebellar hypoplasia type F", "shortest_name_length": 47}
{"curie": "UMLS:C2986962", "names": ["Stage IIA2 Cervical Cancer", "FIGO Stage IIA2 Cervical Carcinoma", "Stage IIA2 Cervical Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA2 Cervical Cancer AJCC v7", "shortest_name_length": 26}
{"curie": "UMLS:C4521614", "names": ["Stage IA Bone Cancer", "Stage IA Bone Cancer AJCC v8", "Stage IA Appendicular Skeleton, Trunk, Skull, and Facial Bones Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Bone Cancer AJCC v8", "shortest_name_length": 20}
{"curie": "MONDO:0015349", "names": ["Progressive cavitating leukoencephalopathy", "Progressive cavitating leucoencephalopathy", "progressive cavitating leukoencephalopathy", "Progressive cavitating leukoencephalopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive cavitating leukoencephalopathy", "shortest_name_length": 42}
{"curie": "MONDO:0018097", "names": ["West", "nodding spasm", "flexion spasm", "west syndrome", "syndrome west", "West Syndrome", "Salaam attack", "West syndrome", "Syndrome, West", "Salaam Attacks", "hypsarrhythmia", "Salaam attacks", "Salaam seizure", "salaam attacks", "attack; salaam", "greeting spasms", "west's syndrome", "salaam seizures", "jackknife spasm", "spasm infantile", "Salaam Seizures", "Salaam seizures", "Epileptic spasm", "Infantile Spasm", "West's syndrome", "Attacks, Salaam", "infantile spasm", "infantile spasms", "eclampsia nutans", "spasm; lightning", "Infantile spasms", "Epileptic spasms", "lightning; spasm", "infantile; spasm", "Lightning Attack", "Infantile Spasms", "Lightning spasms", "spasm; infantile", "infantile salaam", "Seizures, Salaam", "salaam; attack(s)", "Attack, Lightning", "Spasms, Infantile", "Salaam convulsion", "Lightning Attacks", "Attacks, Lightning", "salaam convulsions", "West syndrome (WS)", "Salaam convulsions", "Seizure;infant spasms", "Krampfe salaam attacks", "Hypsarrhythmia syndrome", "West syndrome (disorder)", "Infantile spasms syndrome", "West syndrome (diagnosis)", "Blitz-Nick-salaam attacks", "X-linked infantile spasms", "Epileptic spasms (finding)", "infantile spasms (diagnosis)", "Infantile myoclonic epilepsy", "Infantile spasms - hypsarrythmia", "X-linked infantile spasm syndrome", "infantile spasms with mental retardation", "intellectual disability-hypsarrhythmia syndrome", "infantile spasms-hypsarrhythmia-mental retardation syndrome", "tonic spasms with clustering, arrest of psychomotor development and hypsarrhythmia on EEG"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "West syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0030268", "names": ["DEE6B", "developmental and epileptic encephalopathy 6B", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 6B", "developmental and epileptic encephalopathy 6B, non-Dravet"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy 6B", "shortest_name_length": 5}
{"curie": "MONDO:0025096", "names": ["Snotsiekte", "Malignant Catarrh", "malignant catarrh", "catarrh, malignant", "Catarrh, Malignant", "Malignant Catarrhs", "malignant Catarrhs", "Catarrhs, Malignant", "Catarrhs, malignant", "Malignant head catarrh", "Malignant Catarrhal Fever", "Malignant catarrhal fever", "malignant catarrhal fever", "catarrhal fever, malignant", "malignant catarrhal fevers", "Fever, Malignant Catarrhal", "Malignant Catarrhal Fevers", "Catarrhal Fever, Malignant", "fever, malignant catarrhal", "fevers, malignant catarrhal", "catarrhal fevers, malignant", "Fevers, Malignant Catarrhal", "Catarrhal Fevers, Malignant", "Malignant catarrhal fever (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant catarrh", "shortest_name_length": 10}
{"curie": "MONDO:0015161", "names": ["MCA without intellectual disability", "multiple congenital anomalies/dysmorphic syndrome without intellectual disability", "multiple congenital anomalies without intellectual disability with or without dysmorphism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple congenital anomalies/dysmorphic syndrome without intellectual disability", "shortest_name_length": 35}
{"curie": "UMLS:C0854973", "names": ["Stage II Adenosquamous Lung Cancer", "Stage II Adenosquamous Lung Carcinoma", "Adenosquamous cell lung cancer stage II", "Stage II Adenosquamous Cell Lung Carcinoma", "Stage II Lung Adenosquamous Carcinoma AJCC v7", "Stage II Adenosquamous Cell Carcinoma of Lung", "Stage II Lung Adenosquamous  Carcinoma AJCC v7", "Stage II Adenosquamous Cell Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenosquamous cell lung cancer stage II", "shortest_name_length": 34}
{"curie": "OMIM:618018", "names": ["DRUG METABOLISM, ALTERED, CYP2C8-RELATED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 40}
{"curie": "UMLS:C5555953", "names": ["Uterine Ligament Ependymoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Ligament Ependymoma", "shortest_name_length": 27}
{"curie": "MONDO:0017230", "names": ["autosomal semi-dominant severe lipodystrophic laminopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal semi-dominant severe lipodystrophic laminopathy", "shortest_name_length": 57}
{"curie": "UMLS:C2981273", "names": ["Stage IVA Thyroid Gland Medullary Cancer", "Stage IVA Thyroid Gland Medullary Carcinoma", "Stage IVA Thyroid Gland Medullary Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Thyroid Gland Medullary Carcinoma AJCC v7", "shortest_name_length": 40}
{"curie": "MONDO:0010525", "names": ["Spina Bifida, X-Linked", "spina bifida, X-linked", "SPINA BIFIDA, X-LINKED", "Anencephaly-Spina Bifida", "Neural tube defects X-linked", "neural tube defects, X-linked", "NEURAL TUBE DEFECTS, X-LINKED", "Neural Tube Defects, X-Linked", "X-linked anencephaly-spina bifida", "X-linked anencephaly/spina bifida", "Anencephaly and spina bifida X-linked", "anencephaly and spina bifida X-linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neural tube defects, X-linked", "shortest_name_length": 22}
{"curie": "MONDO:0035320", "names": ["early-onset familial hypoaldosteronism", "Severe aldosterone synthase deficiency", "Early-onset familial hyperreninemic hypoaldosteronism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early-onset familial hypoaldosteronism", "shortest_name_length": 38}
{"curie": "UMLS:C2938972", "names": ["Penile hematoma", "Penile haematoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Penile hematoma", "shortest_name_length": 15}
{"curie": "MONDO:0012630", "names": ["AD13", "Alzheimer Disease 13", "ALZHEIMER DISEASE 13", "Alzheimer disease-13", "Alzheimer disease 13", "Alzheimer's disease 13", "Alzheimer's disease type 13", "Alzheimer's disease 13, late onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alzheimer disease 13", "shortest_name_length": 4}
{"curie": "UMLS:C0267096", "names": ["esophagus injury", "esophageal injury", "Esophageal injury", "injury; esophagus", "esophagus; injury", "Oesophageal injury", "injury of esophagus", "Injury to Esophagus", "Injury of esophagus", "Injury of oesophagus", "Esophageal injury, NOS", "Oesophageal injury, NOS", "Injury of esophagus (disorder)", "injury of esophagus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal injury", "shortest_name_length": 16}
{"curie": "UMLS:C4687397", "names": ["Atypical Type A Thymoma", "Atypical Type A Thymoma Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypical Type A Thymoma", "shortest_name_length": 23}
{"curie": "UMLS:C4521042", "names": ["Down Syndrome", "Complete trisomy 21 syndrome", "Complete Trisomy 21 Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Complete Trisomy 21 Syndrome", "shortest_name_length": 13}
{"curie": "UMLS:C3854603", "names": ["NAIT", "FNAIT", "FNAITP", "Fetal and neonatal alloimmune thrombocytopenia", "Foetal and neonatal alloimmune thrombocytopenia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fetal and neonatal alloimmune thrombocytopenia", "shortest_name_length": 4}
{"curie": "MONDO:0003389", "names": ["EMYOCA", "Epithelial-Myoepithelial Carcinoma", "Epithelial-myoepithelial carcinoma", "epithelial-myoepithelial carcinoma", "[M] Epithelial-myoepithelial carcinoma", "epithelial-myoepithelial carcinoma (diagnosis)", "Epithelial-myoepithelial carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epithelial-myoepithelial carcinoma", "shortest_name_length": 6}
{"curie": "MONDO:0015554", "names": ["typical urticaria pigmentosa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "typical urticaria pigmentosa", "shortest_name_length": 28}
{"curie": "MONDO:0020983", "names": ["heart rupture", "Heart Rupture", "Rupture;heart", "Heart--Rupture", "heart; rupture", "Heart Ruptures", "Cardiac Rupture", "Cardiac rupture", "cardiac rupture", "Cardiac Ruptures", "Rupture of heart", "rupture of heart", "rupture; cardiac", "rupture myocardium", "myocardium rupture", "Rupture;myocardium", "MYOCARDIAL RUPTURE", "Myocardial rupture", "Myocardial Rupture", "myocardial rupture", "rupture of the heart", "cardiac wall rupture", "Free Wall Rupture, Heart", "Cardiac Free Wall Rupture", "Rupture of heart (disorder)", "Ventricular Free Wall Rupture", "cardiac wall rupture (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myocardial rupture", "shortest_name_length": 13}
{"curie": "MONDO:0015650", "names": ["epilepsy syndrome", "epileptic syndrome", "syndromic epilepsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy syndrome", "shortest_name_length": 17}
{"curie": "MONDO:0006247", "names": ["histiocytic and dendritic cell", "histiocytic and dendritic cell tumor", "Histiocytic and dendritic cell tumor", "histiocytic and Dendritic cell tumors", "histiocytic and dendritic cell cancer", "Histiocytic and Dendritic Cell Tumors", "histiocytic and dendritic cell neoplasm", "Histiocytic and Dendritic Cell Neoplasm", "histiocytic and Dendritic cell neoplasms", "Histiocytic and Dendritic Cell Neoplasms"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "histiocytic and dendritic cell neoplasm", "shortest_name_length": 30}
{"curie": "UMLS:C1274355", "names": ["skin strep infection", "strep skin infection", "infection skin strep", "infections skin strep", "streptococcal skin infection", "infection skin streptococcal", "infections skin streptococcal", "streptococcal infection of skin", "Streptococcal infection of skin", "Streptococcal infection of skin (disorder)", "Streptococcal infection of skin (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Streptococcal infection of skin", "shortest_name_length": 20}
{"curie": "MONDO:0021640", "names": ["grade III glioma", "Anaplastic Glioma", "anaplastic glioma", "WHO Grade 3 Glioma", "WHO grade III glioma", "WHO Grade III Glioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "grade III glioma", "shortest_name_length": 16}
{"curie": "MONDO:0800149", "names": ["immunodeficiency, common variable, due to APRIL deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency, common variable, due to APRIL deficiency", "shortest_name_length": 58}
{"curie": "MONDO:0019738", "names": ["aHUS with H factor anomaly", "D-HUS with H factor anomaly", "atypical HUS with H factor anomaly", "atypical hemolytic-uremic syndrome with H factor anomaly", "hemolytic-uremic syndrome without diarrhea with H factor anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical hemolytic-uremic syndrome with H factor anomaly", "shortest_name_length": 26}
{"curie": "MONDO:0014774", "names": ["NBLST7", "neuroblastoma, susceptibility to, 7", "NEUROBLASTOMA, SUSCEPTIBILITY TO, 7", "neuroblastoma, susceptibility to, type 7", "neuroblastoma, susceptibility to, 7; NBLST7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuroblastoma, susceptibility to, 7", "shortest_name_length": 6}
{"curie": "MONDO:0032786", "names": ["NS11", "NOONAN SYNDROME 11", "Noonan syndrome 11", "Noonan Syndrome 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Noonan syndrome 11", "shortest_name_length": 4}
{"curie": "MONDO:0021460", "names": ["salivary gland benign tumor", "Benign Salivary Gland Tumor", "benign salivary gland tumor", "benign salivary gland neoplasm", "Benign salivary gland neoplasm", "Benign tumor of salivary gland", "Benign Salivary Gland Neoplasm", "Benign Tumor of Salivary Gland", "benign tumor of salivary gland", "Salivary Gland Neoplasm, Benign", "salivary gland neoplasm, benign", "Benign tumour of salivary gland", "Benign neoplasm of salivary gland", "Benign Neoplasm of Salivary Gland", "benign neoplasm of salivary gland", "Salivary gland neoplasm benign NOS", "Benign Tumor of the Salivary Gland", "benign tumor of the salivary gland", "Benign Neoplasm of the Salivary Gland", "benign neoplasm of the salivary gland", "saliva-secreting gland benign neoplasm", "Benign tumor of salivary gland (disorder)", "benign neoplasm of salivary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of salivary gland", "shortest_name_length": 27}
{"curie": "UMLS:C2062986", "names": ["Malignant Skull Neoplasm", "malignant neoplasm of skull", "malignant neoplasm of skull (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant neoplasm of skull", "shortest_name_length": 24}
{"curie": "UMLS:C0152246", "names": ["Coredialysis", "iridodialysis", "Iridodialysis", "Iridodialysis (disorder)", "iridodialysis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Iridodialysis", "shortest_name_length": 12}
{"curie": "MONDO:0007730", "names": ["histiocytic dermatoarthritis", "Histiocytic Dermatoarthritis", "HISTIOCYTIC DERMATOARTHRITIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "histiocytic dermatoarthritis", "shortest_name_length": 28}
{"curie": "UMLS:C0854849", "names": ["Relapsed Mycosis Fungoides", "Mycosis Fungoides Relapsed", "Recurrent Mycosis Fungoides", "Mycosis Fungoides Recurrent", "Mycosis fungoides recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mycosis fungoides recurrent", "shortest_name_length": 26}
{"curie": "MONDO:0018794", "names": ["GURDP", "PLA2G4A-related platelet dysfunction", "Phospholipase A2, Group Iva, Deficiency of", "PHOSPHOLIPASE A2, GROUP IVA, DEFICIENCY OF", "PLA2G4A (phospholipase A2 group IVA) related platelet dysfunction", "GASTROINTESTINAL ULCERATION, RECURRENT, WITH DYSFUNCTIONAL PLATELETS", "platelet dysfunction due to cytosolic phospholipase-A2 alpha deficiency", "Platelet dysfunction due to cytosolic phospholipase-A2 alpha deficiency", "Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder", "cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder", "Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder", "shortest_name_length": 5}
{"curie": "MONDO:0044309", "names": ["DBA16", "Diamond-Blackfan anemia 16", "DIAMOND-BLACKFAN ANEMIA 16", "RPL27-related Diamond-Blackfan anemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diamond-Blackfan anemia 16", "shortest_name_length": 5}
{"curie": "MONDO:0000950", "names": ["eye tire", "Eye tired", "TIRED EYE", "Tired eye", "tired eye", "Eyestrain", "eyestrain", "eye tired", "eye strain", "Eye Strain", "tired eyes", "Asthenopia", "asthenopia", "ASTHENOPIA", "Tired eyes", "Eye strain", "eye strains", "fatigue eye", "eye fatigue", "eye; strain", "strain; eye", "Eye Fatigue", "Fatigue, Eye", "eyes fatigue", "eyes strained", "eye straining", "visual fatigue", "Visual Fatigue", "eyes straining", "Fatigue, Visual", "Simple eye strain", "Eye strain (finding)", "tired eyes (symptom)", "accommodative strain", "eye strain (symptom)", "Accommodative strain", "eyestrain (diagnosis)", "eye strain (asthenopia)", "Accommodative asthenopia", "asthenopia; accommodation", "ASTHENOPIA, ACCOMMODATIVE", "accommodation; asthenopia", "Accommodative asthenopia (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "asthenopia", "shortest_name_length": 8}
{"curie": "UMLS:C0877097", "names": ["Application site blister", "Application site vesicles", "Application site blister (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Application site blister", "shortest_name_length": 24}
{"curie": "UMLS:C5556740", "names": ["Vaginal Mucinous Adenocarcinoma, Intestinal-Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Mucinous Adenocarcinoma, Intestinal-Type", "shortest_name_length": 48}
{"curie": "OMIM:138900", "names": ["GOUT1", "UAQTL1", "GOUT SUSCEPTIBILITY 1", "URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 5}
{"curie": "MONDO:0004922", "names": ["Motor delay", "Clumsy child", "clumsy child", "motor skill disorder", "Motor skill disorder", "clumsy child syndrome", "Clumsy Child Syndrome", "Motor Skills Disorder", "Clumsy child syndrome", "motor skills disorder", "disorders motor skill", "Motor Skills Disorders", "child clumsy syndromes", "Clumsy child (finding)", "motor skills disorders", "developmental dyspraxia", "Developmental dyspraxia", "Developmental Dyspraxia", "Clumsiness, motor delay", "dyspraxia; developmental", "developmental; dyspraxia", "Clumsiness - motor delay", "Motor skill disorder, NOS", "Clumsiness - motor retardation", "Motor skill disorder (disorder)", "Motor skill disorder (diagnosis)", "Clumsy child syndrome (diagnosis)", "development coordination disorder", "Development Coordination Disorder", "developmental motor skills disorder", "developmental coordination disorder", "Developmental coordination disorder", "Developmental Coordination Disorder", "Clumsiness - motor delay (disorder)", "developmental disorder; coordination", "Coordination Disorder, Developmental", "Developmental Coordination Disorders", "coordination; developmental disorder", "Developmental motor skills disorders", "developmental motor function disorder", "Developmental coordination disorder NOS", "Developmental disorder of motor function", "developmental disorder clumsy child syndrome", "Developmental coordination disorder (disorder)", "developmental coordination disorder (diagnosis)", "developmental psychological disorder motor skill", "Specific developmental disorder of motor function", "developmental motor function disorder (diagnosis)", "Developmental disorder of motor function (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental coordination disorder", "shortest_name_length": 11}
{"curie": "MONDO:0025114", "names": ["Animal Protozoan Infection", "animal protozoan infection", "Animal Protozoan Infections", "Protozoan Infection, Animal", "animal protozoan infections", "Infection, Animal Protozoan", "infection, animal protozoan", "protozoan infection, animal", "protozoan infections, animal", "infections, animal protozoan", "Infections, Animal Protozoan", "Protozoan Infections, Animal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "protozoan infections, animal", "shortest_name_length": 26}
{"curie": "UMLS:C1332348", "names": ["Atypical Gastric Lymphoid Hyperplasia", "Atypical Gastric Lymphoid Hyperplasia of Stomach", "Atypical Gastric Lymphoid Hyperplasia of the Stomach"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypical Gastric Lymphoid Hyperplasia", "shortest_name_length": 37}
{"curie": "MONDO:0003508", "names": ["choriocarcinoma", "TESTIS, CHORIOCARCINOMA", "Choriocarcinoma of Testis", "choriocarcinoma of testis", "Testicular Choriocarcinoma", "testicular choriocarcinoma", "testicular Choriocarcinoma", "Testicular choriocarcinoma", "choriocarcinoma, testicular", "choriocarcinoma of the testis", "Choriocarcinoma of the Testis", "Testicular choriocarcinoma NOS", "testis cancer, choriocarcinoma", "testis choriocarcinoma (disease)", "testicle cancer, choriocarcinoma", "testicular cancer, choriocarcinoma", "choriocarcinoma of testis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choriocarcinoma of testis", "shortest_name_length": 15}
{"curie": "MONDO:0005601", "names": ["Mucinous carcinoma", "Ovarian Mucinous Carcinoma", "ovarian mucinous carcinoma", "mucinous carcinoma of ovary", "Mucinous Carcinoma of Ovary", "mucinous carcinoma of Ovary", "ovary mucinous adenocarcinoma", "ovarian mucinous adenocarcinoma", "Mucinous Carcinoma of the Ovary", "Ovarian Mucinous Adenocarcinoma", "mucinous carcinoma of the ovary", "mucinous adenocarcinoma of ovary", "Mucinous Adenocarcinoma of Ovary", "Mucinous Adenocarcinoma of the Ovary", "mucinous adenocarcinoma of the ovary", "mucinous adenocarcinoma of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian mucinous adenocarcinoma", "shortest_name_length": 18}
{"curie": "UMLS:C4721927", "names": ["Stage IIIB Uterine Sarcoma", "Stage IIIB Uterine Sarcoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Uterine Sarcoma AJCC v7", "shortest_name_length": 26}
{"curie": "UMLS:C0266770", "names": ["Placenta nappiformis", "Circumvallate placenta", "Circumvallate Placenta", "Placenta Circumvallata", "circumvallate placenta", "placenta circumvallata", "Placenta circumvallata", "Placenta, circumvallate", "placenta; circumvallata", "circumvallata; placenta", "Placenta circumvallata (disorder)", "circumvallate placenta (diagnosis)", "circumvallate placenta (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Placenta circumvallata", "shortest_name_length": 20}
{"curie": "MONDO:0022404", "names": ["retinal ciliopathy due to mutation in Usher gene"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal ciliopathy due to mutation in Usher gene", "shortest_name_length": 48}
{"curie": "MONDO:0017682", "names": ["Kozlowski-Krajewska syndrome", "Kozlowski Krajewska syndrome", "Intellectual disability-polydactyly-uncombable hair syndrome", "intellectual disability-polydactyly-uncombable hair syndrome", "Intellectual disability, polydactyly, uncombable hair syndrome", "intellectual disability, polydactyly, uncombable hair syndrome", "Intellectual disability, polydactyly, uncombable hair syndrome (disorder)", "intellectual disability, polydactyly, uncombable hair syndrome (diagnosis)", "mental retardation, postaxial polydactyly, phalangeal hypoplasia, 2-3 toe syndactyly, unusual face, uncombable hair", "intellectual disability, postaxial polydactyly, phalangeal hypoplasia, 2-3 toe syndactyly, unusual face, uncombable hair"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability-polydactyly-uncombable hair syndrome", "shortest_name_length": 28}
{"curie": "UMLS:C1334775", "names": ["Anaplastic Minor Salivary Gland Carcinoma", "Anaplastic Carcinoma of Minor Salivary Gland", "Minor Salivary Gland Undifferentiated Carcinoma", "Anaplastic Carcinoma of the Minor Salivary Gland", "Undifferentiated Carcinoma of Minor Salivary Gland", "Undifferentiated Carcinoma of the Minor Salivary Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Minor Salivary Gland Undifferentiated Carcinoma", "shortest_name_length": 41}
{"curie": "UMLS:C3897224", "names": ["Untreated Pilocytic Astrocytoma", "Untreated Childhood Pilocytic Astrocytoma", "untreated childhood pilocytic astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Untreated Childhood Pilocytic Astrocytoma", "shortest_name_length": 31}
{"curie": "UMLS:C0263367", "names": ["Koebner", "Köbner phenomenon", "Isomorphic effect", "Kobner phenomenon", "Koebner phenomenon", "koebner phenomenon", "Isomorphic response", "isomorphic response", "Köbner phenomenon (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Köbner phenomenon", "shortest_name_length": 7}
{"curie": "MONDO:0015979", "names": ["hereditary predisposition to infections", "genetic susceptibility to infections due to particular pathogens"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary predisposition to infections", "shortest_name_length": 39}
{"curie": "MONDO:0000953", "names": ["cancer of short bone of lower limb", "malignant neoplasm of short bones of leg", "malignant neoplasm of short bone of lower limb", "Malignant neoplasm of short bone of lower limb", "Malignant neoplasm of short bones of lower limb", "malignant neoplasm of short bones of lower limb", "Malignant neoplasm of short bone of lower limb, NOS", "Malignant neoplasm of short bone of lower limb (disorder)", "malignant neoplasm of short bones of lower limb (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cancer of short bone of lower limb", "shortest_name_length": 34}
{"curie": "MONDO:0001842", "names": ["Sternberg Tumor", "Sternberg tumor", "Cotyledonoid dissecting leiomyoma", "Cotyledonoid Dissecting Leiomyoma", "uterine corpus dissecting leiomyoma", "Uterine Corpus Dissecting Leiomyoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine corpus dissecting leiomyoma", "shortest_name_length": 15}
{"curie": "MONDO:0016909", "names": ["Deletion 10q", "monosomy 10q", "Monosomy 10q", "10q- syndrome", "10q- deletion", "del(10q) syndrome", "10q partial monosomy", "partial monosomy 10q", "10q deletion syndrome", "chromosome 10q monosomy", "Chromosome 10, monosomy 10q", "10q partial monosomy syndrome", "10q partial monosomy (disorder)", "chromosome 10q deletion syndrome", "Partial monosomy of chromosome 10q", "partial deletion of chromosome 10q", "Partial deletion of chromosome 10q", "partial monosomy of chromosome 10q", "Terminal deletion of chromosome 10q", "10q partial monosomy syndrome (diagnosis)", "partial deletion of the long arm of chromosome 10", "Partial monosomy of the long arm of chromosome 10", "Partial deletion of the long arm of chromosome 10", "partial monosomy of the long arm of chromosome 10", "partial monosomy of the long arm of chromosome type 10", "anomaly of chromosome pair 10q partial monosomy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial monosomy of the long arm of chromosome 10", "shortest_name_length": 12}
{"curie": "MONDO:0016511", "names": ["infectious embryofetopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infectious embryofetopathy", "shortest_name_length": 26}
{"curie": "MONDO:0006465", "names": ["THYROID CANCER HURTHLE CELL", "thyroid oncocytic carcinoma", "Thyroid Oncocytic Carcinoma", "Thyroid cancer, Hurthle cell", "HURTHLE CELL THYROID NEOPLASIA", "Thyroid Hurthle Cell Carcinoma", "oncocytic carcinoma of thyroid", "Hurthle Cell Thyroid Neoplasia", "Oncocytic Carcinoma of Thyroid", "thyroid Hurthle cell carcinoma", "THYROID CARCINOMA, HURTHLE CELL", "Cancer of thyroid, Hurthle cell", "Thyroid carcinoma, Hurthle cell", "Thyroid Gland Oncocytic Carcinoma", "Hurthle Cell Carcinoma of Thyroid", "Hurthle cell carcinoma of thyroid", "Oncocytic Carcinoma of the Thyroid", "oncocytic carcinoma of the thyroid", "Hurthle cell thyroid gland carcinoma", "thyroid gland Hurthle cell carcinoma", "Hurthle cell neoplasm of the thyroid", "Hurthle Cell Thyroid Gland Carcinoma", "Thyroid Gland Hurthle Cell Carcinoma", "Hurthle Cell Carcinoma of the Thyroid", "Huerthle cell neoplasm of the thyroid", "Hurthle cell carcinoma of the thyroid", "Hurthle Cell Carcinoma of Thyroid Gland", "Hurthle cell carcinoma of thyroid gland", "thyroid malignant carcinoma hurthle cell", "Hurthle cell carcinoma of the thyroid gland", "Hurthle Cell Carcinoma of the Thyroid Gland", "Hurthle cell carcinoma of thyroid (disorder)", "thyroid gland oncocytic follicular carcinoma", "Thyroid Gland Oncocytic Follicular Carcinoma", "Follicular thyroid cancer, Hurthle cell type", "Thyroid cancer, follicular, Hurthle cell type", "Hurthle cell carcinoma of thyroid (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid gland oncocytic follicular carcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C2987185", "names": ["Pancreatic Mucinous-Cystic Neoplasm, High-Grade", "Pancreatic Mucinous-Cystic Neoplasm, High Grade", "Mucinous cystic neoplasm with high-grade dysplasia", "Pancreatic Mucinous Cystic Neoplasm with High Grade Dysplasia", "Pancreatic Mucinous-Cystic Neoplasm with High Grade Dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Mucinous-Cystic Neoplasm, High Grade", "shortest_name_length": 47}
{"curie": "UMLS:C0877052", "names": ["Congenital choroid plexus cyst", "Congenital choroid plexus cyst (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital choroid plexus cyst", "shortest_name_length": 30}
{"curie": "MONDO:0014975", "names": ["SPG78", "hereditary spastic paraplegia 78", "ATP13A2 hereditary spastic paraplegia", "spastic paraplegia 78 autosomal recessive", "spastic paraplegia 78, autosomal recessive", "SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE", "Autosomal recessive spastic paraplegia type 78", "autosomal recessive spastic paraplegia type 78", "spastic paraplegia 78, autosomal recessive; SPG78", "SPG78 - autosomal recessive spastic paraplegia type 78", "Autosomal recessive spastic paraplegia type 78 (disorder)", "hereditary spastic paraplegia caused by mutation in ATP13A2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive spastic paraplegia type 78", "shortest_name_length": 5}
{"curie": "UMLS:C4763428", "names": ["Locally Advanced Adrenal Gland Pheochromocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Adrenal Gland Pheochromocytoma", "shortest_name_length": 47}
{"curie": "MONDO:0014155", "names": ["ATFB13", "atrial fibrillation familial 13", "ATRIAL FIBRILLATION, FAMILIAL, 13", "atrial fibrillation, familial, 13", "SCN1B familial atrial fibrillation", "atrial fibrillation, familial, type 13", "atrial fibrillation familial 13 (diagnosis)", "familial atrial fibrillation caused by mutation in SCN1B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial fibrillation, familial, 13", "shortest_name_length": 6}
{"curie": "MONDO:0019107", "names": ["RHN", "RHNR", "Rh-Mod", "RH-MOD", "Rh-Null Disease", "Rh-null disease", "Rh mod phenotype", "Rh-null syndrome", "Rh>mod< phenotype", "RH DEFICIENCY SYNDROME", "Rh Deficiency Syndrome", "Rh deficiency syndrome", "RH-null, regulator type", "Rh-Null, Regulator Type", "RH-NULL, REGULATOR TYPE", "Rh<sub>mod</sub> phenotype", "Rhesus deficiency syndrome", "Rh mod blood group phenotype", "Rh>mod< blood group phenotype", "Rh-null disease, regulator type", "RH-NULL DISEASE, REGULATOR TYPE", "Rh deficiency syndrome (disorder)", "Rh<sub>mod</sub> blood group phenotype", "Rh mod blood group phenotype (finding)", "Rh>mod< blood group phenotype (finding)", "RH-NULL HEMOLYTIC ANEMIA, REGULATOR TYPE", "Rh-null hemolytic Anemia, regulator type", "anemia, hemolytic, Rh-null, regulator type", "Rh<sub>mod</sub> blood group phenotype (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rh deficiency syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C0235168", "names": ["Nervous tremulousness", "TREMULOUSNESS NERVOUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nervous tremulousness", "shortest_name_length": 21}
{"curie": "MONDO:0044794", "names": ["mole", "Mole", "Nevus", "moles", "nevus", "Naevus", "naevus", "skin mole", "Benign Mole", "benign nevi", "benign mole", "Mole;benign", "mole (skin)", "Hairy nevus", "Melanocytoma", "NEVUS BENIGN", "benign nevus", "Mole of skin", "Hairy naevus", "benign naevus", "Naevus;benign", "Pigmented nevi", "Benign melanoma", "Pigmented Nevus", "pigmented nevus", "Pigmented nevus", "benign melanoma", "Pigmented moles", "Melanocytic nevi", "Pigmented naevus", "benign skin nevus", "Benign Skin Nevus", "Melanocytic nevus", "melanocytic nevus", "benign skin naevus", "Melanocytic naevus", "melanocytic naevus", "benign skin melanoma", "Benign nevus of skin", "Benign Nevus of Skin", "benign nevus of skin", "Pigmented nevus, NOS", "Benign naevus of skin", "benign pigmented nevus", "benign melanoma of skin", "Melanocytoma (disorder)", "Pigmented nevus of skin", "Benign Nevus of the Skin", "Pigmented naevus of skin", "benign nevus of the skin", "benign melanocytic nevus", "Benign Melanocytic Nevus", "Benign melanocytic nevus", "Benign melanocytic naevus", "Melanocytic nevus of skin", "Melanocytic naevus of skin", "Neoplasm benign;naevus;skin", "benign melanocytic skin nevus", "Benign Skin Melanocytic Nevus", "benign pigmented nevus of skin", "Benign melanocytic nevus of skin", "Benign Melanocytic Nevus of Skin", "benign melanocytic nevus of skin", "Benign melanocytic naevus of skin", "benign pigmented nevus (diagnosis)", "Melanocytic nevus of skin (disorder)", "Benign Melanocytic Nevus of the Skin", "benign melanocytic nevus of the skin", "Pigmented nevus (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign melanocytic skin nevus", "shortest_name_length": 4}
{"curie": "UMLS:C5204611", "names": ["Bladder Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder Melanoma", "shortest_name_length": 16}
{"curie": "UMLS:C1270972", "names": ["MCI", "cognitive disorder mild", "Mild cognitive disorder", "disorder; mild cognitive", "Mild Cognitive Impairment", "cognitive; disorder, mild", "mild cognitive impairment", "disorder; cognitive, mild", "Mild cognitive impairment", "Mild Cognitive Impairments", "Cognitive impairment, mild", "Impairment, Mild Cognitive", "mild; cognitive impairment", "Cognitive Impairment, Mild", "Cognitive Impairments, Mild", "Impairments, Mild Cognitive", "Cognitive impairment, mild,", "Mild cognitive disorder NOS", "Mild cognitive disorder (disorder)", "Mild cognitive disorder (diagnosis)", "mild cognitive impairment (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mild cognitive disorder", "shortest_name_length": 3}
{"curie": "UMLS:C0751669", "names": ["SCA3, Thomas type", "Machado-Joseph disease type 2", "Type II Machado-Joseph Disease", "Machado-Joseph Disease Type II", "Type II Machado Joseph Disease", "Machado Joseph Disease Type II", "Spinocerebellar ataxia, Thomas type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Machado-Joseph Disease Type II", "shortest_name_length": 17}
{"curie": "MONDO:0006927", "names": ["rickettsialpox", "Rickettsiaceae infection", "Rickettsiaceae Infection", "infection, Rickettsiaceae", "Rickettsiaceae Infections", "Infection, Rickettsiaceae", "Infections, Rickettsiaceae", "infections, Rickettsiaceae", "Rickettsiaceae infectious disease", "Rickettsiaceae disease or disorder", "Rickettsiaceae caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rickettsiaceae infectious disease", "shortest_name_length": 14}
{"curie": "MONDO:0018900", "names": ["aseptic abscesses syndrome", "aseptic systemic abscesses", "Aseptic systemic abscesses", "Aseptic abscesses syndrome", "Disseminated aseptic abscesses", "disseminated aseptic abscesses", "corticosteroid-sensitive aseptic abscesses", "Corticosteroid-sensitive aseptic abscess syndrome", "corticosteroid-sensitive aseptic abscess syndrome", "Corticosteroid sensitive aseptic abscess syndrome", "Corticosteroid sensitive aseptic abscess syndrome (disorder)", "Corticosteroid sensitive aseptic abscess syndrome (diagnosis)", "inflammatory disorder corticosteroid sensitive aseptic abscess syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corticosteroid-sensitive aseptic abscess syndrome", "shortest_name_length": 26}
{"curie": "MONDO:0014216", "names": ["CILD28", "primary ciliary dyskinesia 28", "ciliary dyskinesia, primary, 28", "CILIARY DYSKINESIA, PRIMARY, 28", "SPAG1 primary ciliary dyskinesia", "primary ciliary dyskinesia type 28", "ciliary dyskinesia, primary, type 28", "primary ciliary dyskinesia caused by mutation in SPAG1", "primary ciliary dyskinesia 28 with or without situs inversus", "ciliary dyskinesia, primary, 28, with or without situs inversus", "CILIARY DYSKINESIA, PRIMARY, 28, WITH OR WITHOUT SITUS INVERSUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia 28", "shortest_name_length": 6}
{"curie": "UMLS:C3495721", "names": ["MST", "Spitz Melanoma", "Spitzoid melanoma", "Spitzoid Melanoma", "Malignant Spitz Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spitzoid melanoma", "shortest_name_length": 3}
{"curie": "MONDO:0003898", "names": ["pediatric myxoid chondrosarcoma", "childhood myxoid chondrosarcoma", "Pediatric Myxoid Chondrosarcoma", "Childhood Myxoid Chondrosarcoma", "myxoid chondrosarcoma of childhood", "Childhood Extraskeletal Myxoid Chondrosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pediatric myxoid chondrosarcoma", "shortest_name_length": 31}
{"curie": "MONDO:0017340", "names": ["JNA", "Sinonasal Angiofibroma", "nasopharyngeal angiofibroma", "Nasopharyngeal Angiofibroma", "Nasopharyngeal angiofibroma", "Nasopharyngeal Juvenile Angiofibroma", "Juvenile angiofibroma of nasopharynx", "juvenile angiofibroma of nasopharynx", "Juvenile nasopharyngeal angiofibroma", "juvenile nasopharyngeal angiofibroma", "nasopharyngeal juvenile angiofibroma", "juvenile nasopharyngeal angiofibroma (disease)", "Juvenile angiofibroma of nasopharynx (disorder)", "juvenile angiofibroma of nasopharynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile nasopharyngeal angiofibroma", "shortest_name_length": 3}
{"curie": "UMLS:C0025205", "names": ["Experimental Melanoma", "Melanoma, Experimental", "Experimental Melanomas", "Melanomas, Experimental", "Experimental Malignant Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Melanoma, Experimental", "shortest_name_length": 21}
{"curie": "MONDO:0800075", "names": ["dysostosis with predominant vertebral with and without costal involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dysostosis with predominant vertebral with and without costal involvement", "shortest_name_length": 73}
{"curie": "UMLS:C1282522", "names": ["Gastric xanthoma", "Gastric Xanthoma", "Gastric Xanthelasma", "Gastric xanthelasma", "Xanthoma of Stomach", "Xanthoma of the Stomach", "Gastric xanthelasma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Xanthoma", "shortest_name_length": 16}
{"curie": "MONDO:0012532", "names": ["HHT4", "hereditary hemorrhagic telangiectasia type 4", "Telangiectasia, Hereditary Hemorrhagic, Type 4", "TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4", "telangiectasia, hereditary hemorrhagic, type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary hemorrhagic telangiectasia type 4", "shortest_name_length": 4}
{"curie": "MONDO:0012044", "names": ["CDL3A", "lattice corneal dystrophy type 3A", "corneal dystrophy, lattice type 3A", "lattice corneal dystrophy, type 3A", "Lattice Corneal Dystrophy, Type IIIA", "Corneal Dystrophy, Lattice Type IIIA", "lattice corneal dystrophy type III A", "CORNEAL DYSTROPHY, LATTICE TYPE IIIA", "LATTICE CORNEAL DYSTROPHY, TYPE IIIA", "corneal dystrophy, lattice type IIIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal dystrophy, lattice type 3A", "shortest_name_length": 5}
{"curie": "OMIM:618807", "names": ["LPAQTL", "Lp(A) Deficiency, Congenital", "LIPOPROTEIN(a), ELEVATED LEVEL OF", "LIPOPROTEIN(a) DEFICIENCY, CONGENITAL", "Lipoprotein(A) Deficiency, Congenital", "LIPOPROTEIN(a) QUANTITATIVE TRAIT LOCUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 6}
{"curie": "MONDO:0004493", "names": ["papillary pattern testicular yolk sac tumor", "Testicular Yolk Sac Tumor, Papillary Pattern", "testicular yolk sac tumor, papillary pattern"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular yolk sac tumor, papillary pattern", "shortest_name_length": 43}
{"curie": "UMLS:C1708718", "names": ["Unresectable Hepatocellular Cancer", "Localized Unresectable Adult Hepatocellular Carcinoma", "Localized Non-Resectable Adult Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized Unresectable Adult Hepatocellular Carcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0030508", "names": ["SPGF62", "spermatogenic failure 62", "SPERMATOGENIC FAILURE 62"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 62", "shortest_name_length": 6}
{"curie": "UMLS:C3897815", "names": ["Proximal Urethral Cancer", "Proximal Urethral Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Proximal Urethral Carcinoma", "shortest_name_length": 24}
{"curie": "UMLS:C5203917", "names": ["Ocular Graft Versus Host Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ocular Graft Versus Host Disease", "shortest_name_length": 32}
{"curie": "UMLS:C1709871", "names": ["Recurrent Extraosseous Myxoid Chondrosarcoma", "Relapsed Extraskeletal Myxoid Chondrosarcoma", "Recurrent Extraskeletal Myxoid Chondrosarcoma", "Extraskeletal Myxoid Chondrosarcoma, Recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Extraskeletal Myxoid Chondrosarcoma", "shortest_name_length": 44}
{"curie": "MONDO:0011744", "names": ["VMPI", "VMOS", "intraosseous hemangioma", "Intraosseous hemangioma", "Intraosseous haemangioma", "Hemangioma, Intraosseous", "hemangioma, intraosseous", "HEMANGIOMA, INTRAOSSEOUS", "Osseous venous malformation", "osseous venous malformation", "VASCULAR MALFORMATION OSSEOUS", "Vascular Malformation Osseous", "vascular malformation osseous", "Primary intraosseous venous malformation", "primary intraosseous venous malformation", "Vascular Malformation, Primary Intraosseous", "VASCULAR MALFORMATION, PRIMARY INTRAOSSEOUS", "vascular malformation, primary intraosseous", "Primary intraosseous venous malformation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary intraosseous venous malformation", "shortest_name_length": 4}
{"curie": "UMLS:C0525043", "names": ["Reactive attachment disorder", "reactive attachment disorder", "attachment disorder reactive", "Reactive Attachment Disorder", "attachment reactive disorder", "Attachment Disorder, Reactive", "disorder; reactive attachment", "Reactive Attachment Disorders", "attachments disorder reactive", "Disorder, Reactive Attachment", "reactive attachment disorders", "Attachment Disorders, Reactive", "Disorders, Reactive Attachment", "Reactive attachment disorder, NOS", "Reactive attachment disorder (disorder)", "reactive attachment disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reactive Attachment Disorder", "shortest_name_length": 28}
{"curie": "UMLS:C0036216", "names": ["Experimental Sarcoma", "Experimental Sarcomas", "Sarcoma, Experimental", "Sarcomas, Experimental"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sarcoma, Experimental", "shortest_name_length": 20}
{"curie": "MONDO:0004833", "names": ["Policeman Heel", "Policemans Heel", "Policeman's heel", "FASCITIS PLANTAR", "policeman's heel", "Policeman's Heel", "Fascitis plantar", "PLANTAR FASCIITIS", "Plantar fasciitis", "Fasciitis;plantar", "plantar fasciitis", "Plantar Fasciitis", "Fasciitis plantar", "Policeman's Heels", "Heel, Policeman's", "fasciitis; plantar", "Heels, Policeman's", "plantar; fasciitis", "Fasciitis, Plantar", "Plantar fasciitis (disorder)", "plantar fasciitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "plantar fasciitis", "shortest_name_length": 14}
{"curie": "UMLS:C3899981", "names": ["BCLC Stage A Hepatocellular Cancer", "BCLC Stage A Adult Hepatocellular Carcinoma", "Barcelona Clinic Liver Cancer Stage A Adult Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "BCLC Stage A Adult Hepatocellular Carcinoma", "shortest_name_length": 34}
{"curie": "UMLS:C5206639", "names": ["Warty-Basaloid PeIN", "Warty-Basaloid Penile Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Warty-Basaloid Penile Intraepithelial Neoplasia", "shortest_name_length": 19}
{"curie": "MONDO:0006374", "names": ["placenta choriocarcinoma", "Placenta Choriocarcinoma", "Placental choriocarcinoma", "Placental Choriocarcinoma", "placental choriocarcinoma", "Choriocarcinoma of placenta", "choriocarcinoma of placenta", "Choriocarcinoma of Placenta", "choriocarcinoma of the placenta", "Choriocarcinoma of the Placenta", "placenta choriocarcinoma (disease)", "Choriocarcinoma of placenta (disorder)", "choriocarcinoma of placenta (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "placental choriocarcinoma", "shortest_name_length": 24}
{"curie": "MONDO:0700153", "names": ["canine lung adenocarcinoma", "Canine Lung Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canine lung adenocarcinoma", "shortest_name_length": 26}
{"curie": "UMLS:C0233459", "names": ["disorders emotion", "Emotional disorder", "emotional disorder", "EMOTIONAL DISORDER", "disorders emotions", "disorder emotional", "emotional; disorder", "disorders emotional", "disorder; emotional", "Disorder of emotion", "Emotional disorder, NOS", "Disorder of emotion, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Emotional disorder", "shortest_name_length": 17}
{"curie": "UMLS:C0729545", "names": ["ear infection fungal", "Fungal ear infection", "fungal ear infection", "ear fungal infection", "Ear infection fungal", "ear fungal infections", "Fungal ear infection (disorder)", "fungal ear infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fungal ear infection", "shortest_name_length": 20}
{"curie": "MONDO:0011725", "names": ["HBLRCN2", "ani syndrome", "Anis syndrome", "arias syndrome", "Arias syndrome", "Lucey-Arias syndrome", "Crigler-Najjar type 2", "UGT deficiency type 2", "Crigler-Najjar syndrome type 2", "type II Crigler Najjar syndrome", "Crigler-Najjar syndrome, type 2", "Crigler Najjar syndrome, type 2", "bilirubin-UGT deficiency type 2", "Crigler-Najjar syndrome type II", "Bilirubin-UGT deficiency type 2", "Crigler-Najjar syndrome, type II", "CRIGLER-NAJJAR SYNDROME, TYPE II", "Crigler-Najjar Syndrome, Type II", "glucuronyl transferase deficiency type II", "hyperbilirubinemia, Crigler-Najjar type 2", "HYPERBILIRUBINEMIA, CRIGLER-NAJJAR TYPE II", "Crigler-Najjar syndrome, type II (disorder)", "hereditary unconjugated hyperbilirubinemia type 2", "glucuronyl transferase deficiency type II (Crigler-Najjar II)", "bilirubin uridinediphosphate glucuronosyltransferase deficiency type 2", "Bilirubin uridinediphosphate glucuronosyltransferase deficiency type 2", "glucuronyl transferase deficiency type II (Crigler-Najjar II) (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Crigler-Najjar syndrome type 2", "shortest_name_length": 7}
{"curie": "MONDO:0004344", "names": ["malignant hemangiopericytoma", "Malignant Hemangiopericytoma", "Childhood Malignant Hemangiopericytoma", "Malignant Pediatric Hemangiopericytoma", "malignant pediatric hemangiopericytoma", "pediatric malignant hemangiopericytoma", "childhood malignant hemangiopericytoma", "Malignant Childhood Hemangiopericytoma", "malignant childhood hemangiopericytoma", "malignant hemangiopericytoma, pediatric", "malignant hemangiopericytoma, childhood", "hemangiopericytoma, malignant, childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood malignant hemangiopericytoma", "shortest_name_length": 28}
{"curie": "UMLS:C4553578", "names": ["III", "Stage III Thyroid Gland Papillary Cancer", "Stage III Thyroid Gland Papillary Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Thyroid Gland Papillary Carcinoma AJCC v8", "shortest_name_length": 3}
{"curie": "MONDO:0009434", "names": ["IMD43", "B2M DEFICIENCY", "B2M deficiency", "IMMUNODEFICIENCY 43", "immunodeficiency 43", "hypercatabolic hypoproteinemia", "Hypoproteinemia, Hypercatabolic", "beta-2-microglobulin deficiency", "HYPOPROTEINEMIA, HYPERCATABOLIC", "hypoproteinemia, hypercatabolic", "BETA-2-MICROGLOBULIN DEFICIENCY", "Beta-2-microglobulin deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypoproteinemia, hypercatabolic", "shortest_name_length": 5}
{"curie": "MONDO:0018683", "names": ["Acquired ichthyosis", "ichthyosis acquired", "Ichthyosis acquired", "acquired ichthyosis", "fish-skin; acquired", "Acquired Ichthyosis", "ichthyosis acquisita", "ichthyosis; acquired", "Ichthyosis Acquisita", "acquired; ichthyosis", "Ichthyosis, acquired", "ichthyosis, acquired", "Ichthyosis acquisita", "Fish scale disease, acquired", "fish scale disease, acquired", "acquired ichthyosis (disease)", "Acquired ichthyosis (disorder)", "acquired ichthyosis (diagnosis)", "disease (or disorder); fish-skin, acquired"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired ichthyosis", "shortest_name_length": 19}
{"curie": "UMLS:C4055500", "names": ["SAF", "Acral Fibromyxoma", "Digital Fibromyxoma", "Cellular Digital Fibroma", "Superficial Acral Fibromyxoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Superficial Acral Fibromyxoma", "shortest_name_length": 3}
{"curie": "UMLS:C1336168", "names": ["Stage IIA Osteosarcoma", "Stage IIA Osteogenic Sarcoma", "Stage IIA Osteosarcoma AJCC v7", "Stage IIA Osteosarcoma  AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Osteosarcoma AJCC v7", "shortest_name_length": 22}
{"curie": "UMLS:C3853540", "names": ["Samter triad", "Samter syndrome", "Samter's syndrome", "aspirin exacerbated respiratory disease", "Aspirin exacerbated respiratory disease", "Aspirin-exacerbated respiratory disease", "AERD - aspirin exacerbated respiratory disease", "Aspirin exacerbated respiratory disease (disorder)", "aspirin exacerbated respiratory disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aspirin exacerbated respiratory disease", "shortest_name_length": 12}
{"curie": "MONDO:0002649", "names": ["Scrotal Paget Disease", "scrotum Paget disease", "PAGET DISEASE, SCROTUM", "scrotum Paget's disease", "scrotal Paget's disease", "Scrotal Paget's Disease", "Paget's Disease of Scrotum", "Paget's disease of scrotum", "Paget Disease of the Scrotum", "Paget disease of the scrotum", "Paget's disease of the scrotum", "Paget's Disease of the Scrotum", "scrotum mammary Paget's disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scrotum Paget disease", "shortest_name_length": 21}
{"curie": "MONDO:0014047", "names": ["CWS5", "COWDEN SYNDROME 5", "Cowden syndrome 5", "PIK3CA Cowden disease", "Cowden syndrome type 5", "Cowden disease caused by mutation in PIK3CA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cowden syndrome 5", "shortest_name_length": 4}
{"curie": "MONDO:0004756", "names": ["nasal cavity tumor", "Nasal Cavity Tumor", "Tumor of Nasal Cavity", "Tumor of nasal cavity", "tumor of nasal cavity", "nasal cavity neoplasm", "Nasal Cavity Neoplasm", "Tumour of nasal cavity", "neoplasm of nasal cavity", "Neoplasm of nasal cavity", "Neoplasm of Nasal Cavity", "tumor of the nasal cavity", "Tumor of the Nasal Cavity", "neoplasm of the nasal cavity", "nasal cavity benign neoplasm", "Neoplasm of the Nasal Cavity", "Benign Nasal Cavity Neoplasm", "nasal cavity neoplasm (disease)", "Neoplasm of nasal cavity (disorder)", "neoplasm of nasal cavity (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasal cavity neoplasm", "shortest_name_length": 18}
{"curie": "UMLS:C5447384", "names": ["Rectal Large Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rectal Large Cell Neuroendocrine Carcinoma", "shortest_name_length": 42}
{"curie": "UMLS:C0859253", "names": ["Microhemorrhage", "Microhaemorrhage", "Microhemorrhages"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Microhaemorrhage", "shortest_name_length": 15}
{"curie": "MONDO:0019737", "names": ["TMA", "Thrombotic microangiopathy", "Thrombotic Microangiopathy", "thrombotic microangiopathy", "microangiopathy; thrombotic", "Microangiopathy, Thrombotic", "Thrombotic Microangiopathies", "Microangiopathies, Thrombotic", "Thrombotic microangiopathy NOS", "Thrombotic microangiopathy (disorder)", "thrombotic microangiopathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombotic microangiopathy", "shortest_name_length": 3}
{"curie": "MONDO:0009502", "names": ["PDHDD", "pyruvate dehydrogenase E2 deficiency", "Pyruvate dehydrogenase E2 deficiency", "Pyruvate Dehydrogenase E2 Deficiency", "PYRUVATE DEHYDROGENASE E2 DEFICIENCY", "Pyruvate dehydrogenase complex component E2 deficiency", "pyruvate dehydrogenase complex component E2 deficiency", "dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex deficiency", "Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex deficiency", "LACTIC ACIDEMIA DUE TO DEFECT OF E2 LIPOYL TRANSACETYLASE OF THE PYRUVATE DEHYDROGENASE COMPLEX", "Lactic Acidemia due to Defect of E2 Lipoyl Transacetylase of the Pyruvate Dehydrogenase Complex", "lactic acidemia due to defect of E2 lipoyl transacetylase of the pyruvate dehydrogenase Complex", "dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex deficiency", "Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyruvate dehydrogenase E2 deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C0750942", "names": ["Auditory Inattention", "Inattention, Auditory", "Auditory Inattentions", "Inattentions, Auditory"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Auditory Inattention", "shortest_name_length": 20}
{"curie": "MONDO:0008861", "names": ["MCC1D", "MCCD type 1", "Mccd type 1", "MCC deficiency", "Bmcc deficiency", "Mcc1 deficiency", "MCC1 deficiency", "3-MCC deficiency", "MCC 1 deficiency", "3 methylcrotonylglycinuria", "3-methylcrotonylglycinuria", "3-methylcrotonylglycinuria 1", "3-methylcrotonylglycinuria I", "methylcrotonylglycinuria type I", "methylcrotonylglycinuria type 1", "3 alpha methylcrotonylglycinuria 1", "3 Alpha methylcrotonylglycinuria 1", "Methylcrotonyl-Coa carboxylase deficiency", "3-Methylcrotonyl-Coa carboxylase deficiency", "3 Methylcrotonyl-CoA carboxylase deficiency", "methylcrotonoyl-CoA carboxylase 1 deficiency", "3-methylcrotonyl CoA carboxylase 1 deficiency", "deficiency of methylcrotonoyl-Coa carboxylase", "3-METHYLCROTONYL-CoA carboxylase 1 deficiency", "3-methylcrotonyl-CoA carboxylase 1 deficiency", "3-Methylcrotonyl-CoA carboxylase 1 deficiency", "3 Methylcrotonyl-CoA carboxylase 1 deficiency", "3-Methylcrotonyl-Coa carboxylase 1 deficiency", "MCCC1 3-methylcrotonyl-CoA carboxylase deficiency", "3-Methylcrotonyl-Coenzyme A carboxylase deficiency", "3-methylcrotonyl-CoA carboxylase deficiency caused by mutation in MCCC1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "3-methylcrotonyl-CoA carboxylase 1 deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C5419799", "names": ["Colorectal Villous Adenocarcinoma", "Colorectal Adenoma-Like Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Adenoma-Like Adenocarcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C3273009", "names": ["b-HCA", "Beta-Catenin-Activated Hepatocellular Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Beta-Catenin-Activated Hepatocellular Adenoma", "shortest_name_length": 5}
{"curie": "MONDO:0012001", "names": ["Mandibulofacial Dysostosis with Ptosis, Autosomal Dominant", "mandibulofacial dysostosis with ptosis, autosomal dominant", "MANDIBULOFACIAL DYSOSTOSIS WITH PTOSIS, AUTOSOMAL DOMINANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mandibulofacial dysostosis with ptosis, autosomal dominant", "shortest_name_length": 58}
{"curie": "MONDO:0011233", "names": ["RIEG3", "Rieger anomaly", "Axenfeld anomaly", "Rieger syndrome type 3", "Axenfeld-Rieger anomaly", "Rieger Syndrome, Type 3", "Rieger syndrome, type 3", "RIEGER SYNDROME, TYPE 3", "FOXC1 Axenfeld-Rieger syndrome", "Axenfeld-Rieger syndrome Type 3", "Axenfeld-Rieger syndrome type 3", "Axenfeld-Rieger Syndrome, Type 3", "Axenfeld-Rieger syndrome, type 3", "AXENFELD-RIEGER SYNDROME, TYPE 3", "anterior chamber Cleavage syndrome", "ANTERIOR CHAMBER CLEAVAGE SYNDROME", "Anterior Chamber Cleavage Syndrome", "anterior chamber cleavage syndrome", "anterior segment mesenchymal dysgenesis", "Axenfeld-Rieger syndrome Type 3 (diagnosis)", "Axenfeld-Rieger syndrome caused by mutation in FOXC1", "Axenfeld-Rieger anomaly with Cardiac defects and/Or sensorineural hearing loss", "AXENFELD-RIEGER ANOMALY WITH CARDIAC DEFECTS AND/OR SENSORINEURAL HEARING LOSS", "Axenfeld-Rieger anomaly with or without cardiac defects and/or sensorineural hearing loss", "Axenfeld-Rieger Anomaly with or without Cardiac Defects and-or Sensorineural Hearing Loss", "Axenfeld-Rieger anomaly with or without Cardiac defects and/or sensorineural hearing loss"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Axenfeld-Rieger syndrome type 3", "shortest_name_length": 5}
{"curie": "UMLS:C4684877", "names": ["Metastatic Microsatellite Stable Colorectal Cancer", "Metastatic Microsatellite Stable Colorectal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Microsatellite Stable Colorectal Carcinoma", "shortest_name_length": 50}
{"curie": "MONDO:0001347", "names": ["FMD", "FSHD", "FSH dystrophy", "FSH Muscular Dystrophy", "Landouzy-Déjerine; atrophy", "atrophy; Landouzy-Déjerine", "Landouzy-Dejerine myopathy", "Landouzy-Dejerine Dystrophy", "Facioscapulohumeral Atrophy", "Landouzy Dejerine Dystrophy", "Landouzy-Dejerine dystrophy", "Dystrophy, Landouzy-Dejerine", "Facioscapulohumeral myopathy", "dystrophy; Landouzy-Déjerine", "facioscapulohumeral myopathy", "Atrophy, Facioscapulohumeral", "facioscapulohumeral; atrophy", "Landouzy-Déjerine; dystrophy", "atrophy; facioscapulohumeral", "Facioscapulohumeral Atrophies", "myopathy; facioscapulohumeral", "facioscapulohumeral dystrophy", "Facioscapulohumeral dystrophy", "Landouzy-Dejerine Dystrophies", "facioscapulohumeral; myopathy", "Atrophies, Facioscapulohumeral", "Dystrophies, Landouzy-Dejerine", "Facio-Scapulo-Humeral Dystrophy", "Landouzy-Dejerine muscular dystrophy", "LANDOUZY-DEJERINE MUSCULAR DYSTROPHY", "Landouzy Dejerine muscular dystrophy", "Landouzy-Déjérine muscular dystrophy", "Muscular Dystrophy, Landouzy Dejerine", "Muscular dystrophy, Landouzy-Dejerine", "muscular dystrophy, Landouzy-Dejerine", "facioscapulohumeral muscular dystrophy", "MUSCULAR DYSTROPHY FACIOSCAPULOHUMERAL", "FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY", "Facioscapulohumeral muscular dystrophy", "Facioscapulohumeral Muscular Dystrophy", "Facioscapuloperoneal Muscular Dystrophy", "Fascioscapulohumeral muscular dystrophy", "MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL", "Muscular Dystrophy, Facioscapulohumeral", "Dystrophy, Facioscapulohumeral Muscular", "Muscular dystrophy, fascioscapulohumeral", "Facioscapulohumeral Muscular Dystrophies", "dystrophy; muscular, facioscapulohumeral", "muscular; dystrophy, facioscapulohumeral", "Dystrophies, Facioscapulohumeral Muscular", "Muscular Dystrophies, Facioscapulohumeral", "dystrophy; muscular, Landouzy-Déjerine-type", "muscular; dystrophy, Landouzy-Déjerine-type", "FMD - Facioscapulohumeral muscular dystrophy", "FSH - Facioscapulohumeral muscular dystrophy", "FSHD - Facioscapulohumeral muscular dystrophy", "Facioscapulohumeral muscular dystrophy (disorder)", "facioscapulohumeral muscular dystrophy (diagnosis)", "facioscapulohumeral progressive muscular dystrophy", "Progressive muscular dystrophy, Landouzy-Dejerine type", "Facioscapulohumeral Type Progressive Muscular Dystrophy", "Progressive muscular dystrophy, facioscapulohumeral type", "Progressive Muscular Dystrophy, Facioscapulohumeral Type", "Landouzy-Déjerine; dystrophy or facioscapulohumeral atrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "facioscapulohumeral muscular dystrophy", "shortest_name_length": 3}
{"curie": "MONDO:0017128", "names": ["genetic digestive tract tumor", "inherited digestive tract tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited digestive tract tumor", "shortest_name_length": 29}
{"curie": "UMLS:C1336374", "names": ["Stage IVB Larynx Epidermoid Carcinoma", "Stage IVB Laryngeal Epidermoid Carcinoma", "Stage IVB Epidermoid Carcinoma of Larynx", "Stage IVB Larynx Squamous Cell Carcinoma", "Stage IVB Laryngeal Squamous Cell Carcinoma", "Stage IVB Squamous Cell Carcinoma of Larynx", "Stage IVB Epidermoid Carcinoma of the Larynx", "Stage IVB Laryngeal Throat Squamous Cell Cancer", "Stage IVB Squamous Cell Carcinoma of the Larynx", "Stage IVB Laryngeal Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Laryngeal Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 37}
{"curie": "UMLS:C1336072", "names": ["Splenic B Lymphoblastic Lymphoma", "Splenic B-Lymphoblastic Lymphoma", "Splenic Precursor B-Lymphoblastic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Splenic B Lymphoblastic Lymphoma", "shortest_name_length": 32}
{"curie": "MONDO:0013128", "names": ["Hnfj2", "HNFJ2", "ADTKD4", "ADTKD-REN", "FJHN type 2", "REN-associated FJHN", "Ren-Related Kidney Disease", "REN-associated kidney disease", "Familial Juvenile Hyperuricemic Nephropathy 2", "Hyperuricemia, anemia, renal failure syndrome", "Hyperuricemic Nephropathy, Familial Juvenile 2", "REN familial juvenile hyperuricemic nephropathy", "hyperuricemic nephropathy, familial juvenile, 2", "Hyperuricaemia, anaemia, renal failure syndrome", "HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 2", "familial juvenile hyperuricemic nephropathy type 2", "Familial juvenile hyperuricemic nephropathy type 2", "Familial juvenile hyperuricaemic nephropathy type 2", "hyperuricemic nephropathy, familial juvenile, type 2", "tubulointerstitial kidney disease, autosomal dominant, 4", "Hyperuricemia, anemia, renal failure syndrome (disorder)", "TUBULOINTERSTITIAL KIDNEY DISEASE, AUTOSOMAL DOMINANT, 4", "Hyperuricemia, anemia, renal failure syndrome (diagnosis)", "REN-associated familial juvenile hyperuricemic nephropathy", "Renin associated familial juvenile hyperuricemic nephropathy", "Renin associated familial juvenile hyperuricaemic nephropathy", "REN-related autosomal dominant tubulointerstitial kidney disease", "EARLY-ONSET HYPERURICEMIA, ANEMIA, AND PROGRESSIVE KIDNEY FAILURE", "Early-Onset Hyperuricemia, Anemia, And Progressive Kidney Failure", "early-onset hyperuricemia, Anemia, and progressive kidney failure", "nephropathy hereditary hyperuricemia, anemia, renal failure syndrome", "familial juvenile hyperuricemic nephropathy caused by mutation in REN", "autosomal dominant tubulointerstitial kidney disease due to mutations in REN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial juvenile hyperuricemic nephropathy type 2", "shortest_name_length": 5}
{"curie": "MONDO:0017472", "names": ["patella aplasia/hypoplasia, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "patella aplasia/hypoplasia, unilateral", "shortest_name_length": 38}
{"curie": "UMLS:C0553974", "names": ["Radiation-induced fibrous mediastinitis", "Radiation-Induced Fibrous Mediastinitis", "Radiation-induced fibrous mediastinitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radiation-induced fibrous mediastinitis", "shortest_name_length": 39}
{"curie": "UMLS:C5433293", "names": ["PASC", "Long COVID", "Long COVID-19", "Long-Haul COVID", "Long-haul COVID", "Long Haul COVID", "COVID, Long-Haul", "Long-Haul COVIDs", "Long Haul COVID-19", "Long Haul COVID 19", "Post-acute COVID-19", "Long Haul COVID-19s", "COVID-19, Long Haul", "Post-COVID Condition", "Post-COVID Conditions", "Post COVID Conditions", "Long COVID-19 Syndrome", "Post COVID-19 condition", "Post Acute COVID 19 Syndrome", "post-acute COVID-19 syndrome", "Post Acute COVID-19 Syndrome", "Post-acute COVID-19 syndrome", "Post-Acute COVID-19 Syndrome", "Post-Acute COVID-19 Syndromes", "COVID-19 Syndrome, Post-Acute", "Post-acute sequela of COVID-19", "Post-acute COVID-19 (disorder)", "Post-Acute Sequelae of COVID-19", "Post COVID-19 condition (diagnosis)", "Post Acute Sequelae of SARS CoV 2 Infection", "Post-Acute Sequelae of SARS-CoV-2 Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "post-acute COVID-19 syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0032768", "names": ["DEE76", "DECAM", "EIEE76", "Early Infantile Epileptic Encephalopathy 76", "early infantile epileptic encephalopathy 76", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 76", "developmental and epileptic encephalopathy 76", "Developmental and Epileptic Encephalopathy 76", "epileptic encephalopathy, early infantile, 76", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 76", "developmental and epileptic encephalopathy, 76", "Developmental Delay, Epileptic Encephalopathy, Cerebral Atrophy, and Abnormal Myelination", "developmental delay, epileptic endephalopathy, cerebral atrophy, and abnormal myelination", "DEVELOPMENTAL DELAY, EPILEPTIC ENCEPHALOPATHY, CEREBRAL ATROPHY, AND ABNORMAL MYELINATION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 76", "shortest_name_length": 5}
{"curie": "MONDO:0012278", "names": ["PSNP2", "SUPRANUCLEAR PALSY, PROGRESSIVE, 2", "supranuclear palsy, progressive, 2", "Supranuclear Palsy, Progressive, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "supranuclear palsy, progressive, 2", "shortest_name_length": 5}
{"curie": "UMLS:C0275808", "names": ["streptococcal arthritis", "Streptococcal arthritis", "streptoccocal; arthritis", "arthritis; streptoccocal", "Arthritis due to Streptococcus", "Streptococcal arthritis (disorder)", "streptococcal arthritis (diagnosis)", "Streptococcal arthritis or polyarthritis", "Arthritis or polyarthritis due to streptococcus", "Arthritis or Polyarthritis due to Streptococcus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Streptococcal arthritis", "shortest_name_length": 23}
{"curie": "MONDO:0018628", "names": ["HIV-related cancer", "HIV-associated cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HIV-associated cancer", "shortest_name_length": 18}
{"curie": "MONDO:0030941", "names": ["EKVP7", "erythrokeratodermia variabilis et progressiva 7", "ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythrokeratodermia variabilis et progressiva 7", "shortest_name_length": 5}
{"curie": "MONDO:0021350", "names": ["thoracic tumor", "Thoracic Tumor", "thorax neoplasm", "Tumor of Thorax", "tumor of thorax", "Tumor of thorax", "Tumour of thorax", "neoplasms thorax", "Thoracic Neoplasm", "thoracic neoplasm", "Neoplasm, Thoracic", "Neoplasm of Thorax", "Neoplasm of thorax", "neoplasm of thorax", "thoracic neoplasms", "Thoracic Neoplasms", "Neoplasms, Thoracic", "tumor of the thorax", "Tumor of the Thorax", "neoplasm of the thorax", "Neoplasm of the Thorax", "Neoplasm of thorax (disorder)", "neoplasm of thorax (diagnosis)", "thoracic segment of trunk tumor", "tumor of thoracic segment of trunk", "thoracic segment of trunk neoplasm", "neoplasm of thoracic segment of trunk", "thoracic segment of trunk neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplasm of thorax", "shortest_name_length": 14}
{"curie": "UMLS:C0263492", "names": ["Ingrown hair", "ingrown hair", "hairs ingrow", "hair ingrown", "Ingrown;hair", "hairs ingrown", "ingrown hairs", "pili incarnati", "ingrowing hair", "Ingrowing hair", "Pili incarnati", "hair; ingrowing", "pili; incarnati", "incarnati; pili", "ingrowing; hair", "hairs ingrowing", "Pili incarnati (disorder)", "pili incarnati (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pili incarnati (disorder)", "shortest_name_length": 12}
{"curie": "UMLS:C2981612", "names": ["Stage IIB Digestive System Neuroendocrine Tumor", "Stage IIB Digestive System Neuroendocrine Neoplasm", "Stage IIB Gastrointestinal Neuroendocrine Neoplasm", "Stage IIB Digestive System Neuroendocrine Tumor AJCC v7", "Stage IIB Gastrointestinal Neuroendocrine Neoplasm AJCC v7", "Stage IIB Digestive System Neuroendocrine Neoplasm AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Digestive System Neuroendocrine Tumor AJCC v7", "shortest_name_length": 47}
{"curie": "MONDO:0019497", "names": ["Isolated Deafness", "familial deafness", "nonsyndromic deafness", "Nonsyndromic Deafness", "Nonsyndromic Hearing Loss", "nonsyndromic hearing loss", "Undifferentiated Deafness", "isolated genetic deafness", "nonsyndromic genetic deafness", "non-syndromic genetic deafness", "Nonsyndromic Hearing Impairment", "nonsyndromic genetic hearing loss", "nonsyndromic hereditary hearing loss"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nonsyndromic genetic hearing loss", "shortest_name_length": 17}
{"curie": "MONDO:0014363", "names": ["DFNB101", "autosomal recessive deafness 101", "deafness, autosomal recessive 101", "DEAFNESS, AUTOSOMAL RECESSIVE 101", "deafness, autosomal recessive type 101", "autosomal recessive nonsyndromic deafness 101", "GRXCR2 autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 101", "autosomal recessive nonsyndromic deafness type 101", "autosomal recessive nonsyndromic deafness caused by mutation in GRXCR2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 101", "shortest_name_length": 7}
{"curie": "MONDO:0013054", "names": ["Microcephaly, Growth Retardation, Cataract, Hearing Loss, And Unusual Appearance", "microcephaly, growth retardation, cataract, hearing loss, and unusual appearance", "MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUAL APPEARANCE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly, growth retardation, cataract, hearing loss, and unusual appearance", "shortest_name_length": 80}
{"curie": "UMLS:C1336501", "names": ["Sternal Chondromyxoid Fibroma", "Chondromyxoid Fibroma of Sternum", "Chondromyxoid Fibroma of the Sternum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sternal Chondromyxoid Fibroma", "shortest_name_length": 29}
{"curie": "UMLS:C0278652", "names": ["Craniopharyngioma", "Pediatric Craniopharyngioma", "Childhood Craniopharyngioma", "childhood craniopharyngioma", "craniopharyngioma, childhood", "craniopharyngioma, pediatric", "Pediatric Rathke's Pouch Tumor", "Childhood Rathke's Pouch Tumor", "Childhood Tumor of Rathke's Pouch", "Pediatric Tumor of Rathke's Pouch", "Childhood Rathke's Pouch Neoplasm", "Pediatric Rathke's Pouch Neoplasm", "Pediatric Neoplasm of Rathke's Pouch", "Childhood Neoplasm of Rathke's Pouch", "Benign Pediatric Rathke's Pouch Tumor", "Benign Childhood Rathke's Pouch Tumor", "childhood CNS tumor, craniopharyngioma", "pediatric CNS tumor, craniopharyngioma", "CNS tumor, pediatric craniopharyngioma", "CNS tumor, childhood craniopharyngioma", "Benign Childhood Rathke's Pouch Neoplasm", "childhood brain tumor, craniopharyngioma", "brain tumor, childhood craniopharyngioma", "brain tumor, pediatric craniopharyngioma", "pediatric brain tumor, craniopharyngioma", "Benign Pediatric Rathke's Pouch Neoplasm", "Benign Childhood Tumor of Rathke's Pouch", "Benign Pediatric Tumor of Rathke's Pouch", "brain tumor, craniopharyngioma, childhood", "Benign Childhood Neoplasm of Rathke's Pouch", "Benign Pediatric Neoplasm of Rathke's Pouch", "central nervous system tumor, craniopharyngioma, childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Craniopharyngioma", "shortest_name_length": 17}
{"curie": "MONDO:0060592", "names": ["SWCOS", "Sweeney-Cox syndrome", "SWEENEY-COX SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sweeney-Cox syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0017705", "names": ["APVR", "TAPVR", "TAPVR1", "scimitar anomaly", "scimitar syndrome", "pulmonary venous return anomaly", "anomalous pulmonary venous return", "total anomalous pulmonary venous return", "congenital pulmonary venous return anomaly", "congenital pulmonary venous connection anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital pulmonary venous return anomaly", "shortest_name_length": 4}
{"curie": "MONDO:0013075", "names": ["IIAE2", "herpes simplex encephalitis, susceptibility to, 2", "Herpes simplex encephalitis, susceptibility to, type 2", "encephalopathy, acute, infection-induced, susceptibility to, 2", "encephalopathy, acute, infection-induced (Herpes-specific), susceptibility to, 2", "encephalopathy, acute, infection-induced (HERPES-specific), susceptibility to, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "herpes simplex encephalitis, susceptibility to, 2", "shortest_name_length": 5}
{"curie": "UMLS:C5191640", "names": ["Obesity due to leptin receptor gene deficiency", "Obesity due to leptin receptor gene deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Obesity due to leptin receptor gene deficiency", "shortest_name_length": 46}
{"curie": "MONDO:0034189", "names": ["primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome", "shortest_name_length": 100}
{"curie": "MONDO:0016550", "names": ["congenital primary megaureter, obstructed form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital primary megaureter, obstructed form", "shortest_name_length": 46}
{"curie": "MONDO:0016657", "names": ["Del(8)(p11.2)", "Monosomy 8p11.2", "monosomy 8p11.2", "8p11.2 deletion syndrome", "8p11.2 deletion syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "8p11.2 deletion syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0003012", "names": ["SRCC", "RCC w/ sarcomatoid features", "Sarcomatoid Renal Cell Cancer", "sarcomatoid renal cell cancer", "sarcomatoid renal cell carcinoma", "Sarcomatoid Renal Cell Carcinoma", "Renal cell carcinoma, sarcomatoid", "renal cell carcinoma, spindle cell", "Renal cell carcinoma, spindle cell", "sarcomatoid renal cell carcinoma (diagnosis)", "Renal cell carcinoma with sarcomatoid features", "renal cell carcinoma with sarcomatoid features", "Renal cell carcinoma, sarcomatoid (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sarcomatoid renal cell carcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0004784", "names": ["Atopic asthma", "atopic asthma", "asthma atopic", "Asthma, atopic", "asthma; atopic", "atopic; asthma", "asthma allergic", "ASTHMA ALLERGIC", "allergic asthma", "Allergic asthma", "Asthma extrinsic", "Asthma, allergic", "Extrinsic asthma", "ASTHMA EXTRINSIC", "extrinsic asthma", "asthma extrinsic", "extrinsic; asthma", "asthma; extrinsic", "Asthma, allergic NOS", "Allergic atopic asthma", "allergic form of asthma", "extrinsic allergic asthma", "allergic; extrinsic asthma", "Allergic asthma (disorder)", "asthma; allergic extrinsic", "Allergic asthma (diagnosis)", "allergic; asthma, extrinsic", "extrinsic asthma (diagnosis)", "extrinsic asthma with acute exacerbation", "extrinsic asthma with status asthmaticus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "allergic asthma", "shortest_name_length": 13}
{"curie": "UMLS:C1691779", "names": ["Sensory Hearing Loss", "Sensory hearing loss", "sensory hearing loss", "Cochlear Hearing Loss", "Cochlear hearing loss", "Inner ear hearing loss", "Hearing Loss, Cochlear", "Sensory hearing loss NOS", "HEARING DISORDER, COCHLEAR", "Sensory hearing loss (disorder)", "sensory hearing loss (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sensory hearing loss", "shortest_name_length": 20}
{"curie": "MONDO:0001595", "names": ["BHC", "Bch", "chorea", "Chorea", "CHOREA", "Choreas", "Chorea NOS", "Chorea Syndrome", "Chorea Disorder", "chorea disorder", "Chorea syndrome", "chorea was seen", "Chorea (finding)", "Disorder, Chorea", "Chorea Syndromes", "chorea disorders", "disorders chorea", "Choreic movement", "Choreic Movement", "Chorea Disorders", "Syndrome, Chorea", "Syndromes, Chorea", "Choreic movements", "Choreic Movements", "choreic movements", "hereditary chorea", "Choreatic disease", "Disorders, Chorea", "choreatic disease", "Movement, Choreic", "Movements, Choreic", "Choreatic Syndrome", "chorea (diagnosis)", "Choreatic Disorder", "Choreiform movement", "Choreatic Syndromes", "Syndrome, Choreatic", "Disorder, Choreatic", "Choreaform movement", "Choreiform Movement", "choreiform movement", "Choreatic Disorders", "Choreiform Movements", "Disorders, Choreatic", "choreiform movements", "Movement, Choreiform", "Syndromes, Choreatic", "Choreiform movements", "Movements, Choreiform", "benign familial chorea", "hereditary benign chorea", "chorea, benign hereditary", "chorea (physical finding)", "sudden, jerky involuntary movements", "Disorder presenting primarily with chorea", "Disorders presenting primarily with chorea", "sudden, jerky involuntary movements (symptom)", "hereditary progressive chorea without dementia", "Disorder presenting primarily with chorea (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choreatic disease", "shortest_name_length": 3}
{"curie": "UMLS:C0242423", "names": ["Ramsay-Hunt (etiology)", "Ramsay-Hunt (manifestation)", "Ramsay Hunt Paralysis Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ramsay Hunt Paralysis Syndrome", "shortest_name_length": 22}
{"curie": "UMLS:C4683587", "names": ["Lugano Classification Stage IE Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage IE Hodgkin Lymphoma AJCC v8", "shortest_name_length": 55}
{"curie": "UMLS:C0278840", "names": ["DHL, childhood", "childhood DL lymphoma", "pediatric DL lymphoma", "Diffuse Large Cell Lymphoma", "Pediatric Diffuse Large Cell Lymphoma", "Childhood Diffuse Large Cell Lymphoma", "childhood diffuse large cell lymphoma", "pediatric diffuse large cell lymphoma", "diffuse large cell lymphoma, childhood", "lymphoma, diffuse large cell, childhood", "large cell lymphoma, diffuse, childhood", "diffuse histiocytic lymphoma, childhood", "lymphoma, diffuse histiocytic, childhood", "histiocytic lymphoma, diffuse, childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Diffuse Large Cell Lymphoma", "shortest_name_length": 14}
{"curie": "MONDO:0002312", "names": ["Opportunistic mycosis", "opportunistic mycosis", "Opportunistic mycoses", "opportunistic mycoses", "opportunistic; mycosis", "mycosis; opportunistic", "Opportunistic mycosis, NOS", "opportunistic systemic mycoses", "Opportunistic mycosis (disorder)", "opportunistic mycoses (diagnosis)", "mycotic; infection, pathogenic to compromised host only", "infection; mycotic, pathogenic to compromised host only"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "opportunistic mycosis", "shortest_name_length": 21}
{"curie": "MONDO:0025381", "names": ["Avian Leukosis", "avian leukosis", "Avian leukosis", "Avian Leukoses", "Leukosis, Avian", "Leukoses, Avian", "leukosis, Avian", "leukoses, Avian", "Lymphoid leukosis", "lymphoid leukosis", "Avian leukosis (disorder)", "Avian leukosis-sarcoma group"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "avian leukosis", "shortest_name_length": 14}
{"curie": "MONDO:0009806", "names": ["BRKS1", "BRUCK SYNDROME 1", "Bruck syndrome 1", "KUSKOKWIM DISEASE", "Kuskokwim disease", "Kuskokwim syndrome", "FKBP10 Bruck syndrome", "Bruck syndrome type 1", "arthrogryposis-like disorder", "ARTHROGRYPOSIS-LIKE DISORDER", "Arthrogryposis-like disorder", "Arthrogryposis-like syndrome", "Arthrogryposis-like syndrome (disorder)", "Bruck syndrome caused by mutation in FKBP10", "Osteogenesis imperfecta with congenital joint contractures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bruck syndrome 1", "shortest_name_length": 5}
{"curie": "MONDO:0012144", "names": ["WS2D", "Waardenburg syndrome type 2D", "Waardenburg syndrome, type 2D", "Waardenburg Syndrome, Type 2D", "WAARDENBURG SYNDROME, TYPE 2D", "Waardenburg syndrome type IID", "Waardenburg Syndrome, Type IID", "WAARDENBURG SYNDROME, TYPE IID", "SNAI2 Waardenburg syndrome type 2", "Waardenburg syndrome type 2 caused by mutation in SNAI2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Waardenburg syndrome type 2D", "shortest_name_length": 4}
{"curie": "MONDO:0014822", "names": ["Del(15)(q14)", "Monosomy 15q14", "monosomy 15q14", "15q14 microdeletion syndrome", "chromosome 15q14 deletion syndrome", "CHROMOSOME 15q14 DELETION SYNDROME", "15q14 microdeletion syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "15q14 microdeletion syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0017684", "names": ["Disorder of beta and omega amino acid metabolism", "disorder of beta and omega amino acid metabolism", "Disorder of beta and omega amino acid metabolism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of beta and omega amino acid metabolism", "shortest_name_length": 48}
{"curie": "MONDO:0700111", "names": ["bacterial pneumonia, non-human animal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bacterial pneumonia, non-human animal", "shortest_name_length": 37}
{"curie": "UMLS:C3897042", "names": ["SSM", "Smoldering systemic mastocytosis", "Smoldering Systemic Mastocytosis", "smoldering systemic mastocytosis", "Smouldering systemic mastocytosis", "SSM - smoldering systemic mastocytosis", "SSM - smouldering systemic mastocytosis", "Smoldering systemic mastocytosis (disorder)", "Smoldering systemic mastocytosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Smoldering Systemic Mastocytosis", "shortest_name_length": 3}
{"curie": "MONDO:0014396", "names": ["CMD1NN", "dilated cardiomyopathy 1NN", "CARDIOMYOPATHY, DILATED, 1NN", "cardiomyopathy, dilated, 1NN", "dilated cardiomyopathy type 1NN", "cardiomyopathy, dilated, type 1Nn", "RAF1 familial isolated dilated cardiomyopathy", "familial isolated dilated cardiomyopathy caused by mutation in RAF1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1NN", "shortest_name_length": 6}
{"curie": "MONDO:0800105", "names": ["CATATONIA", "Catatonia", "catatonia", "catatonic", "Catatonic", "Catatonias", "Catatonia NOS", "Catatonia, NOS", "Catatonic state", "catatonic state", "catatonia was seen", "Catatonic reaction", "Catatonia (finding)", "catatonia (physical finding)", "demonstrated behavior catatonia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "catatonia", "shortest_name_length": 9}
{"curie": "UMLS:C3873497", "names": ["SARI", "Severe Acute Respiratory Infection", "Severe acute respiratory infection", "Severe acute respiratory infection (SARI)", "Severe acute respiratory infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Severe acute respiratory infection", "shortest_name_length": 4}
{"curie": "OMIM:227240", "names": ["Shep5", "SHEP5", "SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 5", "Skin-Hair-Eye Pigmentation, Variation In, 5", "Skin-Hair-Eye Pigmentation 5, Dark-Fair Skin", "SKIN/HAIR/EYE PIGMENTATION 5, DARK/FAIR SKIN", "Skin-Hair-Eye Pigmentation 5, Dark-Light Eyes", "SKIN/HAIR/EYE PIGMENTATION 5, DARK/LIGHT EYES", "SKIN/HAIR/EYE PIGMENTATION 5, BLACK/NONBLACK HAIR", "Skin-Hair-Eye Pigmentation 5, Black-Nonblack Hair", "SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 5 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 5}
{"curie": "MONDO:0016994", "names": ["MOPD 1", "MOPD types I and III", "Taybi-Linder syndrome", "Taybi Linder syndrome", "Cephaloskeletal dysplasia", "Brachymelic primordial dwarfism", "osteodysplastic primordial dwarfism type I", "Primordial microcephalic dwarfism Crachami type", "primordial microcephalic dwarfism, Crachami type", "Primordial microcephalic dwarfism, Crachami type", "low-birth-weight dwarfism with skeletal dysplasia", "microcephalic osteodysplastic primordial dwarfism type 1", "microcephalic osteodysplastic primordial dwarfism types 1 and 3", "Microcephalic osteodysplastic primordial dwarfism types I and III", "microcephalic osteodysplastic primordial dwarfism types I and III", "Microcephalic osteodysplastic primordial dwarfism Taybi Linder type", "microcephalic osteodysplastic primordial dwarfism, Taybi-Linder type", "Microcephalic osteodysplastic primordial dwarfism, Taybi-Linder type", "Microcephalic osteodysplastic primordial dwarfism types I and III (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephalic osteodysplastic primordial dwarfism types I and III", "shortest_name_length": 6}
{"curie": "MONDO:0002842", "names": ["bacterial gastritis", "Gastritis bacterial", "Bacterial Gastritis", "Bacterial gastritis", "Gastritis bacterial NOS", "Bacteria gastritis (disease)", "Gastritis caused by bacterium", "Bacteria caused gastritis (disease)", "Gastritis caused by bacterium (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bacterial gastritis", "shortest_name_length": 19}
{"curie": "MONDO:0004739", "names": ["UCD", "urea cycle defect", "Urea Cycle Disorder", "Urea cycle disorder", "urea cycle disorder", "cycle disorders urea", "Urea Cycle Disorders", "Disorder, Urea Cycle", "urea cycle disorders", "Disorders, Urea Cycle", "Disorder of urea cycle", "of urea cycle disorder", "Inborn Urea Cycle Disorder", "inborn urea cycle disorder", "Urea Cycle Disorders, Inborn", "metabolic disorder; urea cycle", "urea cycle metabolism disorder", "urea cycle; metabolic disorder", "Urea Cycle Metabolism Disorder", "Disorder of Urea Cycle Metabolism", "disorder of urea cycle metabolism", "Disorders of urea cycle metabolism", "disorder of the urea cycle metabolism", "Disorder of the urea cycle metabolism", "DISORDERS OF THE UREA CYCLE METABOLISM", "Disorder of the urea cycle metabolism, NOS", "Disorder of urea cycle metabolism, unspecified", "Disorder of the urea cycle metabolism (disorder)", "disorder of urea cycle metabolism and ammonia detoxification", "inborn disorder of urea cycle metabolism and ammonia detoxification", "disorder of metabolism of ornithine, citrulline, argininosuccinic acid, arginine and ammonia", "Disorders of metabolism of ornithine, citrulline, argininosuccinic acid, arginine and ammonia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urea cycle disorder", "shortest_name_length": 3}
{"curie": "MONDO:0013992", "names": ["LEPRD", "OBESITY, MORBID", "Leptin Receptor Deficiency", "Leptin receptor deficiency", "LEPTIN RECEPTOR DEFICIENCY", "leptin receptor deficiency", "obesity, morbid, nonsyndromic 2", "obesity due to leptin receptor gene deficiency", "obesity, morbid, due to leptin receptor deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "obesity due to leptin receptor gene deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0004603", "names": ["collagenopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "collagenopathy", "shortest_name_length": 14}
{"curie": "MONDO:0033483", "names": ["ECYT5", "familial erythrocytosis 5", "EPO familial polycythemia", "ERYTHROCYTOSIS, FAMILIAL, 5", "erythrocytosis, familial, 5", "familial polycythemia caused by mutation in EPO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythrocytosis, familial, 5", "shortest_name_length": 5}
{"curie": "MONDO:0700118", "names": ["proximal 18q-", "proximal 18q deletion", "proximal 18q deletion syndrome", "proximal chromosome 18q deletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "proximal chromosome 18q deletion syndrome", "shortest_name_length": 13}
{"curie": "UMLS:C0267209", "names": ["Gastric varices ruptured", "Gastric varices bleeding", "Bleeding gastric varices", "Gastric varices hemorrhage", "Gastric varices haemorrhage", "Bleeding of gastric varices", "gastric varices with hemorrhage", "Bleeding gastric varices (disorder)", "gastric varices with hemorrhage (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bleeding gastric varices", "shortest_name_length": 24}
{"curie": "UMLS:C0334311", "names": ["Acidophil carcinoma", "Acidophil Carcinoma", "Eosinophil Carcinoma", "Eosinophil carcinoma", "Acidophil Adenocarcinoma", "Acidophil adenocarcinoma", "Eosinophil adenocarcinoma", "Eosinophil Adenocarcinoma", "Pituitary Gland Acidophil Carcinoma", "acidophil; carcinoma, unspecified site", "carcinoma; acidophil, unspecified site", "acidophil carcinoma of pituitary gland", "Acidophil carcinoma (morphologic abnormality)", "acidophil carcinoma of pituitary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acidophil carcinoma", "shortest_name_length": 19}
{"curie": "UMLS:C0279703", "names": ["Granular Renal Cell Carcinoma", "Renal granular cell carcinoma", "kidney granular cell carcinoma", "Kidney Granular Cell Carcinoma", "Granular Cell Carcinoma of Kidney", "granular cell carcinoma of kidney", "Granular Cell Carcinoma of the Kidney", "granular cell carcinoma of the kidney", "Granular cell carcinoma of the kidney", "Renal granular cell carcinoma (disorder)", "granular cell carcinoma of kidney (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal granular cell carcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0020242", "names": ["Macular dystrophy", "Genetic Macular Dystrophy", "genetic macular dystrophy", "Hereditary macular dystrophy", "hereditary macular dystrophy", "genetic macular dystrophy (disease)", "Hereditary macular dystrophy (disorder)", "hereditary macular dystrophy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genetic macular dystrophy", "shortest_name_length": 17}
{"curie": "MONDO:0014903", "names": ["BFIC5", "BFIS5", "benign familial infantile seizures 5", "Benign Familial Infantile Seizures, 5", "seizures, benign familial infantile, 5", "SEIZURES, BENIGN FAMILIAL INFANTILE, 5", "SCN8A benign familial infantile epilepsy", "convulsions, benign familial infantile, 5", "CONVULSIONS, BENIGN FAMILIAL INFANTILE, 5", "seizures, benign familial infantile, type 5", "seizures, benign familial infantile, 5; BFIS5", "benign familial infantile epilepsy caused by mutation in SCN8A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "seizures, benign familial infantile, 5", "shortest_name_length": 5}
{"curie": "UMLS:C0751634", "names": ["Carotid Ulcer", "Ulcer, Carotid", "Carotid Ulcers", "Ulcers, Carotid", "Carotid Artery Ulcerating Plaque", "Ulcerating Plaque, Carotid Artery", "Plaque, Ulcerating, Carotid Artery"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carotid Ulcer", "shortest_name_length": 13}
{"curie": "MONDO:0020472", "names": ["Turner syndrome due to structural X chromosome anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Turner syndrome due to structural X chromosome anomalies", "shortest_name_length": 56}
{"curie": "MONDO:0010132", "names": ["TDH1", "dyshormonogenesis", "Dyshormonogenesis", "Thyroid Dyshormonogenesis", "thyroid dyshormonogenesis", "Thyroid dyshormonogenesis", "THYROID DYSHORMONOGENESIS 1", "Thyroid Dyshormonogenesis 1", "nongoitrous hyperthyrotropinemia", "Familial thyroid dyshormonogenesis", "familial thyroid dyshormonogenesis", "thyroid dyshormonogenesis (diagnosis)", "THYROID HORMONOGENESIS, GENETIC DEFECT IN, 1", "Thyroid Hormonogenesis, Genetic Defect in, 1", "Familial thyroid dyshormonogenesis (disorder)", "IODINE ACCUMULATION, TRANSPORT, OR TRAPPING DEFECT", "Iodine Accumulation, Transport, or Trapping Defect", "Hypothyroidism, Congenital, due to Dyshormonogenesis, 1", "HYPOTHYROIDISM, CONGENITAL, DUE TO DYSHORMONOGENESIS, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial thyroid dyshormonogenesis", "shortest_name_length": 4}
{"curie": "UMLS:C2985170", "names": ["Multifocal Glioblastomas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Multifocal Glioblastomas", "shortest_name_length": 24}
{"curie": "MONDO:0012676", "names": ["OPTB4", "osteopetrosis autosomal recessive 4", "autosomal recessive osteopetrosis 4", "osteopetrosis infantile malignant 2", "infantile malignant osteopetrosis 2", "Osteopetrosis, Autosomal Recessive 4", "osteopetrosis, autosomal recessive 4", "Osteopetrosis, Infantile Malignant 2", "OSTEOPETROSIS, INFANTILE MALIGNANT 2", "OSTEOPETROSIS, AUTOSOMAL RECESSIVE 4", "osteopetrosis, infantile malignant 2", "CLCN7 autosomal recessive osteopetrosis", "autosomal recessive osteopetrosis type 4", "osteopetrosis, autosomal recessive type 4", "CLCN7 autosomal recessive malignant osteopetrosis", "autosomal recessive osteopetrosis caused by mutation in CLCN7", "autosomal recessive malignant osteopetrosis caused by mutation in CLCN7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive osteopetrosis 4", "shortest_name_length": 5}
{"curie": "MONDO:0017275", "names": ["Bahemuka Brown syndrome", "Bahemuka-Brown syndrome", "spastic paraplegia facial cutaneous lesions", "Spastic paraplegia facial cutaneous lesions", "spastic paraplegia-facial-cutaneous lesions syndrome", "Spastic paraplegia-facial-cutaneous lesions syndrome", "Spastic paraplegia, facial cutaneous lesion syndrome", "Spastic paraplegia, facial cutaneous lesion syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic paraplegia-facial-cutaneous lesions syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0001915", "names": ["orbit cyst", "orbit; cyst", "cyst; orbit", "orbital cyst", "cyst orbital", "Orbital cyst", "orbital cysts", "Orbital cysts", "Cyst of orbit", "Orbital cyst, NOS", "Cyst of eye socket", "orbital cyst (diagnosis)", "Cyst of orbit (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orbital cyst", "shortest_name_length": 10}
{"curie": "UMLS:C1334425", "names": ["Low Grade Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Grade Malignant Neoplasm", "shortest_name_length": 28}
{"curie": "UMLS:C5669771", "names": ["Diffuse Low Grade Glioma, FGFR1-Mutant", "Diffuse Low-Grade Glioma, FGFR1-Mutant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse Low Grade Glioma, FGFR1-Mutant", "shortest_name_length": 38}
{"curie": "UMLS:C4285843", "names": ["Intra-abdominal fluid collection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intra-abdominal fluid collection", "shortest_name_length": 32}
{"curie": "MONDO:0007740", "names": ["WGN1", "ERVR", "WGVRP", "Wagner Disease", "Wagner disease", "wagner syndrome", "Wagner Syndrome", "Wagner syndrome", "Wagner's disease", "syndrome wagners", "WAGNER SYNDROME 1", "Wagner Syndrome 1", "Wagner syndrome 1", "Wagner syndrome type 1", "Wagner vitreoretinopathy", "WAGNER VITREORETINOPATHY", "Erosive vitreoretinopathy", "EROSIVE VITREORETINOPATHY", "Wagner disease (formerly)", "erosive vitreoretinopathy", "Wagner syndrome (disorder)", "Wagner syndrome (diagnosis)", "VCAN-related vitreoretinopathy", "Vcan-Related Vitreoretinopathy", "Wagner vitreoretinal degeneration", "Wagner vitreoretinal Degeneration", "WAGNER VITREORETINAL DEGENERATION", "Hyaloideoretinal degeneration of Wagner", "HYALOIDEORETINAL DEGENERATION OF WAGNER", "hyaloideoretinal Degeneration of Wagner", "vitreoretinal degeneration, Wagner type", "Vitreoretinal degeneration, Wagner type", "Dominant hyaloideoretinal dystrophy of Wagner", "dominant hyaloideoretinal dystrophy of Wagner"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wagner disease", "shortest_name_length": 4}
{"curie": "MONDO:0041182", "names": ["Sun allergy", "Pruritus estivalis", "Pruritus aestivalis", "polymorphic light eruption", "Polymorphic light eruption", "eruptions light polymorphic", "POLYMORPHOUS LIGHT ERUPTION", "Polymorphous light eruption", "polymorphic photodermatitis", "Polymorphic photodermatitis", "polymorphous light eruption", "Polymorphous Light Eruption", "eruptions light polymorphous", "eruption; polymorphous light", "polymorphous light; eruption", "PLE - Polymorphic light eruption", "Polymorphous light eruption, NOS", "Polymorphic light eruption (disorder)", "polymorphous light eruption (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polymorphic light eruption", "shortest_name_length": 11}
{"curie": "UMLS:C1334546", "names": ["Major Salivary Gland Acinic Cell Carcinoma", "Acinic Cell Carcinoma of Major Salivary Gland", "Major Salivary Gland Acinic Cell Adenocarcinoma", "Acinic Cell Carcinoma of the Major Salivary Gland", "Acinic Cell Adenocarcinoma of Major Salivary Gland", "Acinic Cell Adenocarcinoma of the Major Salivary Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Major Salivary Gland Acinic Cell Carcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0018173", "names": ["acute opioid poisoning"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute opioid poisoning", "shortest_name_length": 22}
{"curie": "UMLS:C5667311", "names": ["Refractory HER2-Positive Breast Carcinoma", "Refractory HER2 Positive Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory HER2-Positive Breast Carcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0014013", "names": ["RBFVD", "riboflavin deficiency", "maternal riboflavin deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maternal riboflavin deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0017538", "names": ["bifid hallux, bilateral", "bifid halluces, bilateral", "bifid great toes, bilateral", "Preaxial polydactyly of toes, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Preaxial polydactyly of toes, bilateral", "shortest_name_length": 23}
{"curie": "MONDO:0014283", "names": ["DFNA56", "autosomal dominant deafness 56", "deafness, autosomal dominant 56", "DEAFNESS, AUTOSOMAL DOMINANT 56", "deafness, autosomal dominant type 56", "autosomal dominant nonsyndromic deafness 56", "TNC autosomal dominant nonsyndromic deafness", "autosomal dominant nonsyndromic hearing loss 56", "autosomal dominant nonsyndromic deafness type 56", "autosomal dominant nonsyndromic deafness caused by mutation in TNC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 56", "shortest_name_length": 6}
{"curie": "MONDO:0004889", "names": ["helicoid choroid dystrophy", "total central choroid atrophy", "total central choroidal atrophy", "Total central choroidal atrophy", "choroidal dystrophy, serpiginous", "Central choroidal atrophy, total", "Choroidal dystrophy, serpiginous", "central gyrate choroidal dystrophy", "Central gyrate choroidal dystrophy", "total central dystrophy of choroid", "Total central dystrophy of choroid", "Choroidal dystrophy, central gyrate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "total central choroidal atrophy", "shortest_name_length": 26}
{"curie": "MONDO:0005291", "names": ["Brain Aneurysm", "aneurysm brain", "brain aneurysm", "Brain aneurysm", "aneurysm; brain", "aneurysms brain", "Aneurysm, Brain", "brain aneurysms", "brain; aneurysm", "Brain Aneurysms", "cranial aneurysm", "CRANIAL ANEURYSM", "Aneurysms, Brain", "Cerebral aneurysm", "cerebral aneurysm", "CEREBRAL ANEURYSM", "Aneurysm cerebral", "Cerebral Aneurysm", "ANEURYSM CEREBRAL", "aneurysm cerebral", "aneurysms cerebral", "Cerebral aneurysms", "cerebral aneurysms", "Aneurysm, Cerebral", "Cerebral Aneurysms", "Aneurysms, Cerebral", "Intracranial Aneurysm", "Cerebral aneurysm NOS", "INTRACRANIAL ANEURYSM", "intracranial aneurysm", "Intracranial aneurysm", "Aneurysm intracranial", "ANEURYSM INTRACRANIAL", "Intracranial aneurysms", "aneurysms intracranial", "intracranial aneurysms", "Aneurysm, Intracranial", "Intracranial Aneurysms", "Aneurysms, Intracranial", "Cerebral artery aneurysm", "cerebral artery aneurysm", "Aneurysm;artery;cerebral", "Cerebral Artery Aneurysm", "Cerebral arterial aneurysm", "Cerebral Arterial Aneurysm", "Intracranial aneurysm, NOS", "aneurysm of cerebral artery", "Aneurysm of Cerebral Artery", "Intracranial aneurysm (disorder)", "Dilatation of the cerebral artery", "Cerebral arterial aneurysm (disorder)", "aneurysm of cerebral artery (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brain aneurysm", "shortest_name_length": 14}
{"curie": "UMLS:C0558066", "names": ["Intrusive Thought", "intrusive thought", "Intrusive thoughts", "intrusive thoughts", "Intrusive thoughts (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intrusive thoughts", "shortest_name_length": 17}
{"curie": "MONDO:0009937", "names": ["PVOD", "Pulmonary venous stenosis", "Pulmonary venous occlusion", "veno occlusive disease lung", "veno-occlusive disease lung", "Pulmonary Venoocclusive Disease", "pulmonary venoocclusive disease", "Pulmonary venoocclusive disease", "Pulmonary Venoocclusive Diseases", "Pulmonary veno-occlusive disease", "pulmonary veno occlusive disease", "Venoocclusive Disease, Pulmonary", "PULMONARY VENO-OCCLUSIVE DISEASE", "Pulmonary Veno-Occlusive Disease", "pulmonary veno-occlusive disease", "Pulmonary Veno Occlusive Disease", "PULMONARY VENO OCCLUSIVE DISEASE", "Pulmonary Veno-Occlusive Diseases", "Veno-Occlusive Disease, Pulmonary", "Venoocclusive Diseases, Pulmonary", "Veno Occlusive Disease, Pulmonary", "Veno-Occlusive Diseases, Pulmonary", "Diseases, Pulmonary Veno-Occlusive", "pulmonary capillary hemangiomatosis", "obstructive disease of the pulmonary veins", "Pulmonary veno-occlusive disease (disorder)", "Pulmonary Veno-Occlusive Disease (disorder)", "pulmonary veno-occlusive disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary venoocclusive disease", "shortest_name_length": 4}
{"curie": "UMLS:C3267019", "names": ["Central nervous system bleeding", "Central nervous system hemorrhage", "Central nervous system haemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central nervous system hemorrhage", "shortest_name_length": 31}
{"curie": "UMLS:C0278607", "names": ["Leiomyosarcoma", "adult leiomyosarcoma", "Adult Leiomyosarcoma", "leiomyosarcoma, adult", "sarcoma, leiomyo-, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Leiomyosarcoma", "shortest_name_length": 14}
{"curie": "MONDO:0025699", "names": ["CSS12", "Coffin-Siris syndrome 12", "COFFIN-SIRIS SYNDROME 12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Coffin-Siris syndrome 12", "shortest_name_length": 5}
{"curie": "UMLS:C4764356", "names": ["Refractory Digestive System Neuroendocrine Neoplasm", "Refractory Gastroenteropancreatic Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Digestive System Neuroendocrine Neoplasm", "shortest_name_length": 51}
{"curie": "MONDO:0012318", "names": ["CLLS1", "Clls1", "LEUKEMIA, CHRONIC LYMPHOCYTIC, SUSCEPTIBILITY TO, 1", "leukemia, chronic lymphocytic, susceptibility to, 1", "leukemia, chronic lymphocytic, susceptibility to, type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukemia, chronic lymphocytic, susceptibility to, 1", "shortest_name_length": 5}
{"curie": "UMLS:C4331419", "names": ["Tissue Kallikrein Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tissue Kallikrein Deficiency", "shortest_name_length": 28}
{"curie": "MONDO:0012079", "names": ["ASPG2", "ASPERGER syndrome, susceptibility to, 2", "ASPERGER SYNDROME, SUSCEPTIBILITY TO, 2", "asperger syndrome, susceptibility to, 2", "Asperger syndrome susceptibility 2, Isolated cases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "asperger syndrome, susceptibility to, 2", "shortest_name_length": 5}
{"curie": "MONDO:0019739", "names": ["aHUS with anti-factor H antibodies", "D-HUS with anti-factor H antibodies", "atypical HUS with anti-factor H antibodies", "atypical hemolytic-uremic syndrome with anti-factor H antibodies", "hemolytic-uremic syndrome without diarrhea with anti-factor H antibodies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical hemolytic-uremic syndrome with anti-factor H antibodies", "shortest_name_length": 34}
{"curie": "MONDO:0008885", "names": ["ESWS", "BSG syndrome", "BSG SYNDROME", "ElSahy-Waters syndrome", "Elsahy-Waters syndrome", "ELSAHY-Waters syndrome", "ELSAHY-WATERS SYNDROME", "BRACHIOSKELETOGENITAL SYNDROME", "brachioskeletogenital syndrome", "Brachioskeletogenital syndrome", "branchioskeletogenital syndrome", "Branchioskeletogenital syndrome", "branchio-skeleto-genital syndrome", "Branchio-skeleto-genital syndrome", "hypertelorism-hypospadias syndrome", "branchio-skeleto-genital (BSG) syndrome", "Branchioskeletogenital syndrome (disorder)", "Branchioskeletogenital syndrome (diagnosis)", "hypospadias-hypertelorism-coloboma and deafness syndrome", "hypospadias, hypertelorism, upper lid coloboma, and mixed-type hearing loss", "hypospadias, hypertelorism, upper 51D coloboma, and mixed-type hearing loss", "Hypospadias, Hypertelorism, Upper Lid Coloboma, and Mixed-Type Hearing Loss", "HYPOSPADIAS, HYPERTELORISM, UPPER LID COLOBOMA, AND MIXED-TYPE HEARING LOSS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Elsahy-Waters syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0017027", "names": ["primary ILD specific to adulthood", "primary interstitial lung disease specific to adulthood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary interstitial lung disease specific to adulthood", "shortest_name_length": 33}
{"curie": "MONDO:0000263", "names": ["laryngotracheitis", "Laryngotracheitis", "Laryngotracheitis NOS", "tracheitis; laryngitis", "Laryngotracheitis, NOS", "laryngitis; tracheitis", "Acute laryngotracheitis", "acute laryngotracheitis", "chronic laryngotracheitis", "Chronic laryngotracheitis", "Tracheitis with laryngitis", "chronic; laryngotracheitis", "laryngotracheitis; chronic", "Laryngitis/tracheitis acute", "Acute laryngitis/tracheitis", "Laryngotracheitis acute NOS", "Laryngotracheitis (disorder)", "Laryngo-tracheitis acute NOS", "Laryngotracheitis chronic NOS", "laryngotracheitis (diagnosis)", "Acute laryngitis and tracheitis", "laryngitis; tracheitis, chronic", "tracheitis; laryngitis, chronic", "Tracheitis with acute laryngitis", "Acute tracheitis with laryngitis", "Chronic laryngitis with tracheitis", "Acute laryngitis and/or tracheitis", "Acute laryngotracheitis (disorder)", "Chronic tracheitis with laryngitis", "acute laryngotracheitis (diagnosis)", "Tracheitis, chronic, with laryngitis", "Chronic laryngotracheitis (disorder)", "chronic laryngotracheitis (diagnosis)", "Acute tracheitis with acute laryngitis", "Tracheitis (acute) with laryngitis (acute)", "Chronic laryngitis with chronic tracheitis", "Acute laryngitis and/or tracheitis (disorder)", "chronic; tracheitis, with laryngitis (chronic)", "chronic; laryngitis, with tracheitis (chronic)", "laryngitis; chronic, with tracheitis (chronic)", "Laryngitis, chronic, with tracheitis (chronic)", "tracheitis; chronic, with laryngitis (chronic)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laryngotracheitis", "shortest_name_length": 17}
{"curie": "MONDO:0006513", "names": ["ER- breast cancer", "estrogen-receptor negative breast cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "estrogen-receptor negative breast cancer", "shortest_name_length": 17}
{"curie": "MONDO:0008947", "names": ["PFBC", "BSPDC", "Fahr disease", "Fahr's disease", "basal ganglia calcification", "cerebrovascular ferrocalcinosis", "primary familial brain calcification", "idiopathic basal ganglia calcification", "basal ganglia calcification, idiopathic", "bilateral striopallidodentate calcinosis", "Basal ganglia degeneration with calcification", "basal ganglia degeneration with calcification", "Basal ganglia degeneration with calcification (disorder)", "basal ganglia degeneration with calcification (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bilateral striopallidodentate calcinosis", "shortest_name_length": 4}
{"curie": "UMLS:C0016662", "names": ["open fracture", "FRACTURE OPEN", "Open fracture", "Fracture-open", "Open Fracture", "Fracture, Open", "OPEN FRACTURES", "fractures open", "Fracture, open", "Open Fractures", "open fractures", "Fractures, Open", "fracture opened", "Compound Fracture", "compound fracture", "fracture compound", "Fracture;compound", "Compound fracture", "Compound Fractures", "Fracture, Compound", "Fracture, compound", "compound fractures", "Fractures, Compound", "Fracture, open, NOS", "Fracture, compound, NOS", "Open fracture (disorder)", "open fracture (diagnosis)", "Fracture of unspecified bone, open", "Fracture, open (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fractures, Open", "shortest_name_length": 13}
{"curie": "UMLS:C2346457", "names": ["II", "Multiple Myeloma Stage II", "Stage II Multiple Myeloma", "Stage II Plasma Cell Myeloma", "ISS Stage II Multiple Myeloma", "ISS Stage II Plasma Cell Myeloma", "ISS Stage II Multiple Myeloma/Plasma Cell Myeloma", "International Staging System Stage II Multiple Myeloma", "International Staging System Stage II Plasma Cell Myeloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ISS Stage II Plasma Cell Myeloma", "shortest_name_length": 2}
{"curie": "UMLS:C0236830", "names": ["Neuroleptic induced parkinsonism", "Neuroleptic-induced Parkinsonism", "Neuroleptic-induced parkinsonism", "neuroleptic-induced parkinsonism", "Parkinsonism caused by neuroleptic drug", "neuroleptic-induced parkinsonism (diagnosis)", "Parkinsonism caused by neuroleptic drug (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neuroleptic-induced parkinsonism", "shortest_name_length": 32}
{"curie": "UMLS:C5206746", "names": ["Refractory Systemic Anaplastic Large Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Systemic Anaplastic Large Cell Lymphoma", "shortest_name_length": 50}
{"curie": "UMLS:C1302539", "names": ["VAGINAL CONDYLOMA", "Vaginal Condyloma", "Vaginal Condyloma Acuminatum", "Condyloma acuminata of vagina", "Condylomata Acuminata of Vagina", "Condylomata Acuminata of the Vagina", "Condyloma acuminata of vagina (disorder)", "Condyloma acuminata of vagina (diagnosis)", "warts genital condyloma acuminata of vagina"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Condyloma acuminata of vagina", "shortest_name_length": 17}
{"curie": "MONDO:0001247", "names": ["Sociophobia", "Sociophobias", "social phobia", "phobia social", "Social Phobia", "Social phobia", "social phobias", "Social phobias", "phobias social", "Phobia, Social", "social; phobia", "Social Phobias", "phobia; social", "Social neurosis", "social; neurosis", "neurosis; social", "Social phobia, NOS", "social phobia disorder", "Social Evaluation Fear", "disorder social phobia", "Social anxiety disorder", "Social Anxiety Disorder", "Evaluation Fear, Social", "social anxiety disorder", "disorders phobia social", "anxiety disorder social", "Disorder, Social Anxiety", "anxiety disorders social", "anxiety disorder; social", "Social phobia (disorder)", "Social Anxiety Disorders", "Social Evaluation Phobia", "Anxiety Disorder, Social", "Fear of Social Evaluation", "social phobia (diagnosis)", "Social Evaluation Phobias", "Phobia, Social Evaluation", "Social phobia, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "social phobia", "shortest_name_length": 11}
{"curie": "MONDO:0011742", "names": ["HSCR7", "Hirschsprung disease, susceptibility to, 7", "HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hirschsprung disease, susceptibility to, 7", "shortest_name_length": 5}
{"curie": "MONDO:0020647", "names": ["MFRG", "microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome", "MICROCEPHALY, FACIAL DYSMORPHISM, RENAL AGENESIS, AND AMBIGUOUS GENITALIA SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C1707544", "names": ["Epithelioid fibrous histiocytoma", "Epithelioid Fibrous Histiocytoma", "Cutaneous Epithelioid Fibrous Histiocytoma", "Skin Fibrous Histiocytoma, Epithelioid Variant", "Cutaneous Fibrous Histiocytoma, Epithelioid Variant", "Epithelioid fibrous histiocytoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epithelioid fibrous histiocytoma", "shortest_name_length": 32}
{"curie": "MONDO:0000649", "names": ["sensory system cancer", "cancer of sensory system", "malignant sensory system neoplasm", "malignant neoplasm of sensory system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sensory system cancer", "shortest_name_length": 21}
{"curie": "MONDO:0009036", "names": ["Pfeiffer syndrome 2", "cardiocranial syndrome", "Cardiocranial syndrome", "Pfeiffer cardiocranial syndrome", "Pfeiffer Cardiocranial syndrome", "PFEIFFER CARDIOCRANIAL SYNDROME", "Pfeiffer Singer Zschiesche syndrome", "Pfeiffer-Singer-Zschiesche syndrome", "Cardiocranial syndrome Pfeiffer type", "Pfeiffer-type cardiocranial syndrome", "cardiocranial syndrome, Pfeiffer type", "Cardiocranial syndrome, Pfeiffer type", "Cardiocranial syndrome Pfeiffer type (disorder)", "craniosynostosis-congenital heart disease-intellectual disability syndrome", "Craniosynostosis-congenital heart disease-intellectual disability syndrome", "Craniosynostosis with congenital heart disease and intellectual disability syndrome", "Sagittal craniostenosis with congenital heart disease, mental deficiency and mandibular ankylosis", "sagittal craniostenosis with congenital heart disease, mental deficiency and mandibular ankylosis", "CRANIOSTENOSIS, SAGITTAL, WITH CONGENITAL HEART DISEASE, MENTAL DEFICIENCY, AND MANDIBULAR ANKYLOSIS", "craniostenosis, sagittal, with congenital heart disease, mental deficiency, and mandibular ankylosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiocranial syndrome, Pfeiffer type", "shortest_name_length": 19}
{"curie": "UMLS:C4289691", "names": ["Diffuse Astrocytoma, IDH-Wildtype", "Diffuse astrocytoma, IDH-wildtype", "Diffuse Astrocytoma, IDH Wild Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse Astrocytoma, IDH-Wildtype", "shortest_name_length": 33}
{"curie": "UMLS:C5670968", "names": ["ALPS-Related Lymphoma", "Autoimmune Lymphoproliferative Syndrome-Related Lymphoma", "Autoimmune Lymphoproliferative Syndrome-Associated Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Autoimmune Lymphoproliferative Syndrome-Related Lymphoma", "shortest_name_length": 21}
{"curie": "MONDO:0005436", "names": ["postoperative ventricular dysfunction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postoperative ventricular dysfunction", "shortest_name_length": 37}
{"curie": "UMLS:C0860552", "names": ["retinal pigment epitheliopathy", "Retinal pigment epitheliopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retinal pigment epitheliopathy", "shortest_name_length": 30}
{"curie": "UMLS:C0677709", "names": ["Stage II Diffuse Large Cell Lymphoma", "noncontiguous stage II adult diffuse large cell lymphoma", "stage II noncontiguous adult diffuse large cell lymphoma", "Stage II NonContiguous Adult Diffuse Large Cell Lymphoma", "NonContiguous Adult Diffuse Large Cell Lymphoma Stage II", "noncontiguous adult diffuse large cell lymphoma stage II", "Non-Contiguous Stage II Adult Diffuse Large Cell Lymphoma", "non-contiguous adult diffuse large cell lymphoma stage II", "Non-Contiguous Adult Diffuse Large Cell Lymphoma Stage II", "Stage II Non-Contiguous Adult Diffuse Large Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Non-Contiguous Adult Diffuse Large Cell Lymphoma", "shortest_name_length": 36}
{"curie": "MONDO:0015783", "names": ["Prader-Willi syndrome (Type 1)", "Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1", "shortest_name_length": 30}
{"curie": "MONDO:0011333", "names": ["LFSS", "Lfss", "M syndrome", "M Syndrome", "M SYNDROME", "LIGHT FIXATION SEIZURE SYNDROME", "Light Fixation Seizure Syndrome", "light fixation seizure syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "light fixation seizure syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0012143", "names": ["sdCHC", "SDCHCN", "ChC type 2", "hereditary cryohydrocytosis type 2", "stomatin-deficient cryohydrocytosis", "hereditary cryohydrocytosis with reduced stomatin", "Stomatin-Deficient Cryohydrocytosis with Neurologic Defects", "stomatin-deficient cryohydrocytosis with neurologic defects", "STOMATIN-DEFICIENT CRYOHYDROCYTOSIS WITH NEUROLOGIC DEFECTS", "GLUT1 DEFICIENCY SYNDROME WITH PSEUDOHYPERKALEMIA AND HEMOLYSIS", "GLUT1 deficiency syndrome with pseudohyperkalemia and hemolysis", "Cryohydrocytosis, Stomatin-Deficient, with Mental Retardation, Seizures, Cataracts, and Massive Hepatosplenomegaly", "cryohydrocytosis, stomatin-deficient, with mental retardation, seizures, cataracts, and massive hepatosplenomegaly", "CRYOHYDROCYTOSIS, STOMATIN-DEFICIENT, WITH MENTAL RETARDATION, SEIZURES, CATARACTS, AND MASSIVE HEPATOSPLENOMEGALY", "cryohydrocytosis, stomatin-deficient, with intellectual disability, seizures, cataracts, and massive hepatosplenomegaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary cryohydrocytosis with reduced stomatin", "shortest_name_length": 5}
{"curie": "MONDO:0019600", "names": ["XP", "Kaposi Disease", "KAPOSI DISEASE", "Kaposi disease", "Kaposis Disease", "Kaposi's Disease", "Kaposi Dermatosis", "Kaposi dermatosis", "xeroderma of Kaposi", "Xeroderma of Kaposi", "xeroderma pigmentosa", "xeroderma pigmentosum", "Xeroderma pigmentosum", "XERODERMA PIGMENTOSUM", "pigmentosum xeroderma", "Xeroderma Pigmentosum", "xeroderma; pigmentosum", "pigmentosum; xeroderma", "Atrophoderma Pigmentosum", "atrophoderma pigmentosum", "Atrophoderma pigmentosum", "atrophoderma; pigmentosum", "pigmentosum; atrophoderma", "pigmented epitheliomatosis", "Xeroderma pigmentosum, NOS", "Pigmented Epitheliomatosis", "XP - Xeroderma pigmentosum", "Pigmented epitheliomatosis", "epitheliomatosis; pigmented", "angioma pigmentosum atrophicum", "Angioma pigmentosum atrophicum", "Xeroderma Pigmentosum Syndrome", "Angioma Pigmentosum Atrophicum", "Xeroderma pigmentosum syndrome", "xeroderma pigmentosum syndrome", "Xeroderma pigmentosum (disorder)", "xeroderma pigmentosum (diagnosis)", "Melanosis Lenticularis Progressiva", "Melanosis lenticularis progressiva", "melanosis lenticularis progressiva", "melanosis; lenticularis progressiva", "lenticularis progressiva; melanosis", "pigmentation; congenital, xeroderma pigmentosum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "xeroderma pigmentosum", "shortest_name_length": 2}
{"curie": "MONDO:0006841", "names": ["Lymphatic Endothelioma", "Lymphangioendothelioma", "lymphangioendothelioma", "Endothelioma, Lymphatic", "Lymphatic Endotheliomas", "Lymphangioendotheliomas", "Endotheliomas, Lymphatic", "Lymphangioendothelioma, NOS", "Benign lymphangioendothelioma", "Acquired progressive lymphangioma", "Acquired Progressive Lymphangioma", "acquired progressive lymphangioma", "Acquired progressive lymphangioma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphangioendothelioma", "shortest_name_length": 22}
{"curie": "UMLS:C1512510", "names": ["Human Papillomavirus-Related Urethral Squamous Cell Carcinoma", "Human Papilloma Virus-Related Urethral Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Human Papillomavirus-Related Urethral Squamous Cell Carcinoma", "shortest_name_length": 61}
{"curie": "MONDO:0003549", "names": ["Adenosquamous Bile Duct Carcinoma", "bile duct adenosquamous carcinoma", "bile duct Adenosquamous carcinoma", "adenosquamous bile duct carcinoma", "Bile duct adenosquamous carcinoma", "Bile Duct Adenosquamous Carcinoma", "Adenosquamous Carcinoma of Bile Duct", "adenosquamous carcinoma of bile duct", "Adenosquamous Carcinoma of the Bile Duct", "adenosquamous carcinoma of the bile duct", "Extrahepatic Bile Duct Adenosquamous Carcinoma", "extrahepatic bile duct adenosquamous carcinoma", "adenosquamous carcinoma of extrahepatic bile duct", "adenosquamous carcinoma of the extrahepatic bile duct", "adenosquamous carcinoma of extrahepatic bile duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenosquamous bile duct carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0002729", "names": ["MRTK", "renal rhabdoid tumor", "Renal Rhabdoid Tumor", "renal Rhabdoid tumor", "kidney rhabdoid tumor", "Kidney Rhabdoid Tumor", "kidney rhabdoid cancer", "renal rhabdoid neoplasm", "Renal Rhabdoid Neoplasm", "Rhabdoid Tumour of Kidney", "rhabdoid tumour of kidney", "Rhabdoid Neoplasm of Kidney", "rhabdoid neoplasm of kidney", "rhabdoid tumor of the kidney", "Rhabdoid tumor (kidney) (RT)", "Rhabdoid Tumor of the Kidney", "Rhabdoid tumor of the kidney", "Rhabdoid Tumour of the Kidney", "rhabdoid tumour of the kidney", "Rhabdoid tumour of the kidney", "Rhabdoid Neoplasm of the Kidney", "rhabdoid neoplasm of the kidney", "Malignant Rhabdoid Tumor of Kidney", "Rhabdoid Tumor of the Kidney (RTK)", "rhabdoid tumor of the kidney (RTK)", "malignant rhabdoid tumor of kidney", "malignant rhabdoid tumor of the kidney", "Malignant Rhabdoid Tumor of the Kidney", "malignant rhabdoid tumor of kidney (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rhabdoid tumor of the kidney", "shortest_name_length": 4}
{"curie": "UMLS:C1336074", "names": ["Splenic T Lymphoblastic Lymphoma", "Splenic T-Lymphoblastic Lymphoma", "Splenic Precursor T-Lymphoblastic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Splenic T Lymphoblastic Lymphoma", "shortest_name_length": 32}
{"curie": "MONDO:0009887", "names": ["DIP", "RBILD", "ILD, desquamative", "ILD, DESQUAMATIVE", "Desquamative interstitial pneumonia", "desquamative interstitial pneumonia", "Desquamative Interstitial Pneumonia", "PNEUMONIA, DESQUAMATIVE INTERSTITIAL", "desquamative interstitial pneumonitis", "Desquamative interstitial pneumonitis", "INTERSTITIAL LUNG DISEASE, DESQUAMATIVE", "Interstitial Lung Disease, Desquamative", "interstitial lung disease, desquamative", "desquamative interstitial pneumonia (DIP)", "Intra-alveolar accumulation of macrophages", "DIP - Desquamative interstitial pneumonitis", "Desquamative interstitial pneumonia (disorder)", "pneumonia, desquamative interstitial, familial", "Pneumonia, Desquamative Interstitial, Familial", "PNEUMONIA, DESQUAMATIVE INTERSTITIAL, FAMILIAL", "familial desquamative interstitial pneumonitis", "desquamative interstitial pneumonia (diagnosis)", "Filling of the alveoli with alveolar macrophages", "PNEUMONITIS, DESQUAMATIVE INTERSTITIAL, FAMILIAL", "Pneumonitis, Desquamative Interstitial, Familial", "pneumonitis, desquamative interstitial, familial", "Interstitial Pneumonitis, Desquamative, Familial", "INTERSTITIAL PNEUMONITIS, DESQUAMATIVE, FAMILIAL", "interstitial pneumonitis, desquamative, familial", "desquamative interstitial pneumonitis (diagnosis)", "respiratory bronchiolitis interstitial lung disease", "Respiratory Bronchiolitis Interstitial Lung Disease", "Respiratory bronchiolitis interstitial lung disease", "Filling of the alveoli with desquamated epithelial cells", "pneumonitis idiopathic nonspecific interstitial desquamative", "respiratory bronchiolitis-associated interstitial lung disease", "respiratory bronchiolitis interstitial lung disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "desquamative interstitial pneumonia", "shortest_name_length": 3}
{"curie": "MONDO:0007044", "names": ["ADOHR", "ACRDYS1", "Acrodysostosis 1", "acrodysostosis 1", "ACRODYSOSTOSIS 1 WITH OR WITHOUT HORMONE RESISTANCE", "Acrodysostosis 1 with or without hormone resistance", "acrodysostosis 1 with or without hormone resistance", "acrodysostosis 1, with or without hormone resistance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acrodysostosis 1 with or without hormone resistance", "shortest_name_length": 5}
{"curie": "MONDO:0017511", "names": ["split hand, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "split hand, unilateral", "shortest_name_length": 22}
{"curie": "UMLS:C3899281", "names": ["Early Inflammatory Arthritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Early Inflammatory Arthritis", "shortest_name_length": 28}
{"curie": "UMLS:C3874987", "names": ["Orthotopic Ureterocele", "Orthotopic ureterocele", "Orthotopic ureterocoele", "Intravesical Ureterocele", "Orthotopic ureterocele (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Orthotopic ureterocele", "shortest_name_length": 22}
{"curie": "UMLS:C5400677", "names": ["NSAA", "Moderate Aplastic Anemia", "Non-Severe Aplastic Anemia", "Non Severe Aplastic Anemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Severe Aplastic Anemia", "shortest_name_length": 4}
{"curie": "MONDO:0009801", "names": ["osteodysplasia familial Anderson type", "Familial osteodysplasia Anderson type", "familial osteodysplasia, Anderson type", "Familial osteodysplasia, Anderson type", "osteodysplasia, familial, Anderson type", "Osteodysplasia, Familial, Anderson Type", "OSTEODYSPLASIA, FAMILIAL, ANDERSON TYPE", "Familial osteodysplasia Anderson type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial osteodysplasia, Anderson type", "shortest_name_length": 37}
{"curie": "UMLS:C3891404", "names": ["Metastatic Gastrointestinal Carcinoid Tumor", "Metastatic Gastrointestinal Neuroendocrine Tumor G1", "Metastatic Digestive System Neuroendocrine Tumor G1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Digestive System Neuroendocrine Tumor G1", "shortest_name_length": 43}
{"curie": "MONDO:0004745", "names": ["Priapism", "PRIAPISM", "priapism", "hulseyism", "Priapisms", "Mentulagra", "CHRONIC ERECTION", "chronic erection", "Pathologic erection", "Priapism (disorder)", "priapism (diagnosis)", "Priapism, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "priapism", "shortest_name_length": 8}
{"curie": "UMLS:C2826322", "names": ["RAEB-F", "RAEB with Fibrosis", "Myelodysplastic Syndrome with Excess Blasts and Fibrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myelodysplastic Syndrome with Excess Blasts and Fibrosis", "shortest_name_length": 6}
{"curie": "UMLS:C0521706", "names": ["Cataract unilateral", "unilateral cataract", "CATARACT UNILATERAL", "Unilateral cataract", "cataract unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cataract unilateral", "shortest_name_length": 19}
{"curie": "UMLS:C0849925", "names": ["Ventricular failure", "Failure;ventricular", "ventricular failure", "Ventricular failure NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ventricular failure", "shortest_name_length": 19}
{"curie": "MONDO:0005998", "names": ["itch; harvest", "harvest; itch", "Trombiculiasis", "trombiculiasis", "Trombiculiases", "Trombiculidae infectious disease", "Trombiculidae disease or disorder", "Trombiculidae caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trombiculiasis", "shortest_name_length": 13}
{"curie": "MONDO:0015268", "names": ["MSK", "sponge kidney", "Sponge kidney", "Sponge Kidney", "kidney sponge", "Kidney, Sponge", "KIDNEY, SPONGE", "Sponge Kidneys", "sponge kidneys", "Sponge kidneys", "Kidneys, Sponge", "Sponge kidney NOS", "Cacchi Ricci Disease", "Cacchi Ricci disease", "Cacchi-Ricci disease", "Cacchi-Ricci syndrome", "Disease, Cacchi Ricci", "Cacchi-Ricci Syndrome", "Ricci Disease, Cacchi", "Cacchi Ricci Syndrome", "Syndrome, Cacchi-Ricci", "Medullary sponge kidney", "kidney sponge medullary", "Medullary Sponge Kidney", "MEDULLARY SPONGE KIDNEY", "kidney medullary sponge", "medullary sponge kidney", "kidneys medullary sponge", "KIDNEY, MEDULLARY SPONGE", "Sponge Kidney, Medullary", "Medullary Sponge Kidneys", "Sponge Kidneys, Medullary", "Precalyceal Canalicular Ectasia", "Precalicial canalicular ectasia", "Precalyceal canalicular ectasia", "Ectasia, Precalyceal Canalicular", "Canalicular Ectasia, Precalyceal", "Precalyceal Canalicular Ectasias", "Ectasias, Precalyceal Canalicular", "Canalicular Ectasias, Precalyceal", "Medullary sponge kidney (disorder)", "medullary sponge kidney (diagnosis)", "cystic dilatation of renal collecting tubes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "medullary sponge kidney", "shortest_name_length": 3}
{"curie": "MONDO:0005070", "names": ["tumor", "TUMOR", "Tumor", "tumors", "Cancer", "Tumors", "tumour", "Tumour", "tumours", "NEOPLASM", "Neoplasm", "Oncology", "neoplasm", "Neoplasms", "NEOPLASMS", "neoplasms", "Neoplasia", "tumor NOS", "NEOPLASIA", "neoplasia", "Tumor, NOS", "Neoplasias", "New growth", "neoplasias", "Tumour, NOS", "neoplasm NOS", "NEOPLASM NOS", "Neoplasm NOS", "Neoplasm, NOS", "tumor disease", "Neoplasms, NOS", "NEOPLASM (NOS)", "new growth NOS", "other neoplasm", "NEOPLASMS, NOS", "Other Neoplasm", "Tumor Syndrome", "NG - New growth", "Neoplastic growth", "Neoplastic Growth", "neoplastic growth", "neoplasm (disease)", "Neoplastic disease", "Neoplastic Disease", "neoplastic disease", "neoplastic syndrome", "Neoplastic Syndrome", "Neoplastic syndrome", "cell process disease", "Abnormal tissue mass", "NG - Neoplastic growth", "Oncological abnormality", "Neoplastic disease, NOS", "Neoplastic syndrome, NOS", "Neoplastic disease (disorder)", "disease of cellular proliferation", "Neoplasm (morphologic abnormality)", "malignant, benign, and unspecified neoplasms, cysts, polyps", "neoplasm - benign, malignant, unspecified (including cysts, polyps)", "Neoplasms benign, malignant and unspecified (incl cysts and polyps)", "malignant, benign, and unspecified neoplasms, cysts, polyps (diagnosis)", "Neoplasms benign, malignant and unspecified (including cysts and polyps)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplasm", "shortest_name_length": 5}
{"curie": "MONDO:0006706", "names": ["Bifidobacteriales infection", "Bifidobacteriales Infection", "infection, Bifidobacteriales", "Bifidobacteriales Infections", "Infection, Bifidobacteriales", "infections, Bifidobacteriales", "Infections, Bifidobacteriales", "Bifidobacteriales infectious disease", "Bifidobacteriales disease or disorder", "Bifidobacteriales caused disease or disorder", "commensal Bifidobacteriales infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bifidobacteriales infectious disease", "shortest_name_length": 27}
{"curie": "MONDO:0008005", "names": ["CSCF", "Forney syndrome", "Forney-Robinson-Pascoe syndrome", "Forney Robinson Pascoe syndrome", "Cardiospondylocarpofacial Syndrome", "Cardiospondylocarpofacial syndrome", "cardiospondylocarpofacial syndrome", "CARDIOSPONDYLOCARPOFACIAL SYNDROME", "Cardiospondylocarpofacial syndrome (disorder)", "mitral regurgitation-deafness-skeletal anomalies syndrome", "Mitral regurgitation-deafness-skeletal anomalies syndrome", "Mitral regurgitation-hearing loss-skeletal anomalies syndrome", "Congenital heart disease, deafness, and skeletal malformations", "congenital heart disease, deafness, and skeletal malformations", "Mitral regurgitation with deafness and skeletal anomalies syndrome", "Mitral Regurgitation, Conductive Deafness, and Fusion of Cervical Vertebrae and of Carpal and Tarsal Bones", "mitral regurgitation, conductive deafness, and fusion of cervical vertebrae and of carpal and tarsal bones", "MITRAL REGURGITATION, CONDUCTIVE DEAFNESS, AND FUSION OF CERVICAL VERTEBRAE AND OF CARPAL AND TARSAL BONES", "[OBSOLETE] Mitral Regurgitation, Conductive Deafness, and Fusion of Cervical Vertebrae and of Carpal and Tarsal Bones"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiospondylocarpofacial syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C4527176", "names": ["Stage 0", "Stage 0 Cutaneous (Skin) Melanoma", "Pathologic Stage 0 Cutaneous Melanoma AJCC v8", "Pathologic Stage 0 Melanoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage 0 Cutaneous Melanoma AJCC v8", "shortest_name_length": 7}
{"curie": "MONDO:0011975", "names": ["KOS", "UPD(14)pat", "Kagami-Ogata syndrome", "KAGAMI-Ogata syndrome", "Kagami Ogata syndrome", "KAGAMI-OGATA SYNDROME", "Paternal uniparental disomy 14", "paternal uniparental disomy 14", "Kagami Ogata syndrome (disorder)", "Kagami Ogata syndrome (diagnosis)", "uniparental disomy, paternal, chromosome 14", "UNIPARENTAL DISOMY, PATERNAL, CHROMOSOME 14", "Uniparental disomy, paternal, chromosome 14", "paternal uniparental disomy of chromosome 14", "Paternal uniparental disomy of chromosome 14", "paternal uniparental disomy of chromosome type 14", "Uniparental disomy of paternal origin of chromosome 14", "Uniparental disomy of paternal origin of chromosome 14 (disorder)", "Multiple congenital anomalies due to 14q32.2 maternally expressed gene defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paternal uniparental disomy of chromosome 14", "shortest_name_length": 3}
{"curie": "MONDO:0014357", "names": ["VSVS", "MRD24", "IDDISBAS", "Vulto-van Silfout-de Vries syndrome", "VULTO-VAN SILFHOUT-DE VRIES SYNDROME", "autosomal dominant mental retardation 24", "mental retardation, autosomal dominant 24", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 24", "autosomal dominant intellectual disability 24", "mental retardation, autosomal dominant type 24", "intellectual disability, autosomal dominant 24", "intellectual disability, autosomal dominant type 24", "autosomal dominant non-syndromic intellectual disability 24", "DEAF1 autosomal dominant non-syndromic intellectual disability", "autosomal dominant non-syndromic intellectual disability caused by mutation in DEAF1", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH IMPAIRED EXPRESSIVE SPEECH AND BEHAVIORAL ABNORMALITIES, WITH OR WITHOUT SEIZURES", "intellectual developmental disorder with impaired expressive speech and behavioral abnormalities, with or without seizures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 24", "shortest_name_length": 4}
{"curie": "UMLS:C0010695", "names": ["CYSTOCELE", "cystocele", "Cystocele", "Cystocoele", "cystoceles", "cystocoele", "Cystocele NOS", "bladder hernia", "Cystocele, NOS", "vesical hernia", "hernia bladder", "cystocele bladder", "bladder cystocele", "Fallen Urinary Bladder", "Urinary Bladder Prolapse", "Prolapse, Urinary Bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cystocele", "shortest_name_length": 9}
{"curie": "UMLS:C1335719", "names": ["Recurrent Peripheral Primitive Neuroectodermal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Peripheral Primitive Neuroectodermal Tumor", "shortest_name_length": 52}
{"curie": "UMLS:C1333555", "names": ["FIGO Stage IIIA GTT", "FIGO Stage IIIA Gestational Trophoblastic Tumor", "FIGO Stage IIIA Gestational Trophoblastic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Stage IIIA Gestational Trophoblastic Tumor", "shortest_name_length": 19}
{"curie": "MONDO:0002628", "names": ["surface osteosarcoma", "Surface Osteosarcoma", "peripheral osteosarcoma", "Peripheral Osteosarcoma", "bone surface (peripheral) osteosarcoma", "Bone Surface (Peripheral) Osteosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peripheral osteosarcoma", "shortest_name_length": 20}
{"curie": "MONDO:0005641", "names": ["Aleutian disease", "Mink Aleutian disease", "aleutian mink disease", "Aleutian Mink Disease", "Aleutian mink disease", "Mink Disease, Aleutian", "Disease, Aleutian Mink", "Aleutian Disease of Mink", "Aleutian disease (disorder)", "Aleutian mink disease virus infectious disease", "Aleutian mink disease virus disease or disorder", "Aleutian mink disease virus caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aleutian mink disease", "shortest_name_length": 16}
{"curie": "MONDO:0008577", "names": ["toe, misshapen", "TOE, MISSHAPEN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "toe, misshapen", "shortest_name_length": 14}
{"curie": "MONDO:0032814", "names": ["PADMAL", "Dementia, Hereditary Multi-Infarct, Swedish Type", "DEMENTIA, HEREDITARY MULTI-INFARCT, SWEDISH TYPE", "Pontine autosomal dominant microangiopathy with leucoencephalopathy", "Pontine autosomal dominant microangiopathy with leukoencephalopathy", "MICROANGIOPATHY AND LEUKOENCEPHALOPATHY, PONTINE, AUTOSOMAL DOMINANT", "microangiopathy and leukoencephalopathy, pontine, autosomal dominant", "PADMAL - pontine autosomal dominant microangiopathy with leucoencephalopathy", "PADMAL - pontine autosomal dominant microangiopathy with leukoencephalopathy", "Pontine autosomal dominant microangiopathy with leukoencephalopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microangiopathy and leukoencephalopathy, pontine, autosomal dominant", "shortest_name_length": 6}
{"curie": "UMLS:C0275378", "names": ["poisons tobacco", "Tobacco poisoning", "tobacco poisoning", "Cigarette poisoning", "poisoning by tobacco", "Nicotiana tabacum poisoning", "poisoning tobacco cigarettes", "poisoning by tobacco (diagnosis)", "Nicotiana tabacum poisoning (disorder)", "poisoning tobacco cigarettes (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nicotiana tabacum poisoning", "shortest_name_length": 15}
{"curie": "MONDO:0017424", "names": ["brachydactyly", "isolated brachydactyly", "nonsyndromic brachydactyly", "non-syndromic brachydactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-syndromic brachydactyly", "shortest_name_length": 13}
{"curie": "UMLS:C5204530", "names": ["Refractory Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Adenocarcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0007950", "names": ["Mastocytosis", "MASTOCYTOSIS", "mastocytoses", "mastocytosis", "Mastocytosis NOS", "MAST cell disease", "Mast cell disease", "mast cell disease", "Mast Cell Disease", "Mast cell disorder", "mast cell disorder", "disease; mast cell", "mast cell; disease", "cell diseases mast", "cell disorders mast", "urticaria pigmentosa", "mast cell hyperplasia", "Mast cell hyperplasia", "Mast cell disorder (disorder)", "congenital cutaneous mastocytosis", "Congenital cutaneous mastocytosis", "congenital cutaneous mastocytosis (diagnosis)", "Mast cell hyperplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mastocytosis", "shortest_name_length": 12}
{"curie": "MONDO:0004322", "names": ["non-gestational ovarian choriocarcinoma", "Non-Gestational Ovarian Choriocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-gestational ovarian choriocarcinoma", "shortest_name_length": 39}
{"curie": "MONDO:0014668", "names": ["MC4DN13", "CEMCOX4", "COA6 fatal infantile encephalocardiomyopathy", "mitochondrial complex IV deficiency nuclear type 13", "MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 13", "mitochondrial complex IV deficiency, nuclear type 13", "fatal infantile encephalocardiomyopathy caused by mutation in COA6", "fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 4", "CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 4", "cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 4", "cardioencephalomyopathy, fatal infantile, due to cytochrome C oxidase deficiency type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 4", "shortest_name_length": 7}
{"curie": "UMLS:C4683154", "names": ["Stage IV Posterior Uveal Melanoma AJCC v8", "Stage IV Choroidal and Ciliary Body Melanoma", "Stage IV Choroidal and Ciliary Body Melanoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Choroidal and Ciliary Body Melanoma AJCC v8", "shortest_name_length": 41}
{"curie": "MONDO:0004005", "names": ["rete ovarii adenoma", "Rete Ovarii Adenoma", "Adenoma of rete ovarii", "ADENOMA, RETE OVARII, BENIGN", "adenoma, rete ovarii, benign", "Adenoma of rete ovarii (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rete ovarii adenoma", "shortest_name_length": 19}
{"curie": "MONDO:0013496", "names": ["IGAN2", "IgA nephropathy, susceptibility to, 2", "IgA NEPHROPATHY, SUSCEPTIBILITY TO, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IgA nephropathy, susceptibility to, 2", "shortest_name_length": 5}
{"curie": "UMLS:C2938937", "names": ["Acute Hemorrhagic Edema of Infancy", "Acute hemorrhagic edema of infancy", "Acute haemorrhagic oedema of infancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute hemorrhagic edema of infancy", "shortest_name_length": 34}
{"curie": "UMLS:C4727409", "names": ["Recurrent Submandibular Gland Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Submandibular Gland Carcinoma", "shortest_name_length": 39}
{"curie": "MONDO:0009717", "names": ["SJS", "SJS1", "Schwartz", "SJA Syndrome", "SJA SYNDROME", "burton syndrome", "Burton syndrome", "schwartz syndrome", "aberfeld syndrome", "Schwartz syndrome", "Aberfeld syndrome", "Schwartz's syndrome", "Aberfeld's syndrome", "Catel Hempel syndrome", "Catel-Hempel syndrome", "Schwartz-Jampel disease", "Schwartz-Jampel syndrome", "jampel schwartz syndrome", "Schwartz-Jampel Syndrome", "Schwartz Jampel syndrome", "schwartz-jampel syndrome", "Schwartz Jampel Syndrome", "schwartz jampel syndrome", "SCHWARTZ-JAMPEL SYNDROME", "Burton skeletal dysplasia", "Myotonic Chondrodystrophy", "Schwartz-Janipel syndrome", "burton skeletal dysplasia", "Myotonic chondrodystrophy", "myotonic chondrodystrophy", "Chondrodystrophic myotonia", "Chondrodystrophic Myotonia", "CHONDRODYSTROPHIC MYOTONIA", "Chondrodystrophy, Myotonic", "chondrodystrophic myotonia", "myotonia chondrodystrophica", "Myotonia, Chondrodystrophic", "chondrodystrophic; myotonia", "myotonia; chondrodystrophic", "Myotonia chondrodystrophica", "chondrodystrophia myotonica", "Osteochondromuscular dystrophy", "osteochondromuscular dystrophy", "Schwartz-Jampel syndrome (SJS)", "Schwartz-Jampel syndrome type 1", "Schwartz Jampel Aberfeld syndrome", "Schwartz-Jampel-Aberfeld Syndrome", "Schwartz-Jampel-Aberfeld syndrome", "SCHWARTZ-JAMPEL-ABERFELD SYNDROME", "Syndrome, Schwartz-Jampel-Aberfeld", "Schwartz-Jampel syndrome (disorder)", "Congenital myotonic chondrodystrophy", "chondrodystrophic myotonia (diagnosis)", "Schwartz-Jampel-Aberfeld (SJA) syndrome", "spondylo-epimetaphyseal dysplasia with myotonia", "Spondylo-Epimetaphyseal Dysplasia With Myotonia", "chondrodystrophic myotonia (Schwartz-Jampel syndrome)", "Congenital blepharophimosis, myopia, myopathy syndrome", "Catel-Hempel type dysostosis enchondralis metaepiphysaria", "dysostosis enchondralis metaepiphysaria, Catel-Hempel type", "Dysostosis enchondralis metaepiphysaria, Catel-Hempel type", "myotonic myopathy, dwarfism, chondrodystrophy, ocular and facial anomalies", "Myotonic myopathy, dwarfism, chondrodystrophy, ocular and facial anomalies", "myotonic myopathy dwarfism chondrodystrophy and ocular and facial abnormalities", "Myotonic Myopathy, Dwarfism, Chondrodystrophy, And Ocular And Facial Abnormalities", "myotonic myopathy, dwarfism, chondrodystrophy, and ocular and Facial abnormalities", "MYOTONIC MYOPATHY, DWARFISM, CHONDRODYSTROPHY, AND OCULAR AND FACIAL ABNORMALITIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Schwartz-Jampel syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C3898147", "names": ["Neonatal HIE", "Neonatal Hypoxic Ischemic Encephalopathy", "Hypoxic ischemic encephalopathy neonatal", "Hypoxic ischaemic encephalopathy neonatal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypoxic ischemic encephalopathy neonatal", "shortest_name_length": 12}
{"curie": "UMLS:C1112313", "names": ["Gastrointestinal mucosal disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal mucosal disorder", "shortest_name_length": 33}
{"curie": "UMLS:C5670675", "names": ["Stage II Cervical Cancer FIGO 2009", "Stage II Cervical Carcinoma FIGO 2009"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Cervical Cancer FIGO 2009", "shortest_name_length": 34}
{"curie": "MONDO:0007633", "names": ["FRIEDREICH ATAXIA, SO-CALLED, WITH OPTIC ATROPHY AND SENSORINEURAL DEAFNESS", "Friedreich Ataxia, So-Called, with Optic Atrophy and Sensorineural Deafness", "Friedreich ataxia, so-called, with optic atrophy and sensorineural deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Friedreich ataxia, so-called, with optic atrophy and sensorineural deafness", "shortest_name_length": 75}
{"curie": "MONDO:0001976", "names": ["chorea gravidarum", "Chorea gravidarum", "Chorea Gravidarum", "Chorea Gravidarums", "Gravidarum, Chorea", "Pregnancy-Induced Chorea", "Pregnancy-Induced Choreas", "Chorea, Pregnancy Induced", "Chorea, Pregnancy-Induced", "Choreas, Pregnancy-Induced", "Chorea gravidarum syndrome", "Chorea gravidarum (disorder)", "chorea gravidarum (diagnosis)", "Pregnancy-Associated Choreoathetoses", "Pregnancy-Associated Choreoathetosis", "Choreoathetoses, Pregnancy-Associated", "Choreoathetosis, Pregnancy Associated", "Choreoathetosis, Pregnancy-Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chorea gravidarum", "shortest_name_length": 17}
{"curie": "UMLS:C0919935", "names": ["Adrenal abscess", "Adrenal Gland Abscess", "Adrenal gland abscess", "Abscess of adrenal gland", "Abscess of adrenal gland (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abscess of adrenal gland", "shortest_name_length": 15}
{"curie": "MONDO:0001984", "names": ["candidiasis of skin", "Candidal perionyxis", "Candidal paronychia", "candidal paronychia", "candidal perionyxis", "paronychia candidal", "Candidosis of nail fold", "Candidiasis, paronychial", "Candidiasis of nail fold", "Candidiasis of skin and nail", "Candidiasis of skin and nails", "candidiasis of skin and nails", "Candidal paronychia (disorder)", "Candidal perionyxis (disorder)", "Candidal paronychia (diagnosis)", "candidal perionyxis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "candidal paronychia", "shortest_name_length": 19}
{"curie": "MONDO:0007125", "names": ["ANKG", "tongue-tie", "Tongue-tie", "Tongue Tie", "Tongue tie", "tie tongue", "tongue tie", "TONGUE TIE", "Tongue Ties", "tongue tied", "ties tongue", "Tongue tied", "tied tongue", "'TONGUE-TIE'", "'tongue-Tie'", "ANKYLOGLOSSIA", "Ankyloglossia", "ankyloglossia", "Ankyloglossias", "Tongue tie (disorder)", "tongue tie (diagnosis)", "FUSED TO FLOOR OF MOUTH", "FUSED to floor of mouth", "[OBSOLETE] Ankyloglossia", "Ankyloglossia congenital", "ANKYLOGLOSSIA WITH OR WITHOUT TOOTH ANOMALIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ankyloglossia", "shortest_name_length": 4}
{"curie": "UMLS:C0398563", "names": ["HK1 Deficiency", "Hexokinase Deficiency", "hexokinase deficiency", "Hexokinase deficiency", "deficiency hexokinase", "Deficiency of hexokinase", "HK - Hexokinase deficiency", "Deficiency of hexokinase type IV", "hexokinase deficiency (diagnosis)", "Erythrocyte Hexokinase Deficiency", "Deficiency of hexokinase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Deficiency of hexokinase (disorder)", "shortest_name_length": 14}
{"curie": "UMLS:C5419027", "names": ["Extrarenal Rhabdoid Tumor of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extrarenal Rhabdoid Tumor of the Ovary", "shortest_name_length": 38}
{"curie": "MONDO:0019077", "names": ["warty dyskeratoma", "Warty dyskeratoma", "Warty Dyskeratoma", "Follicular dyskeratoma", "follicular dyskeratoma", "Follicular Dyskeratoma", "Warty dyskeratoma (disorder)", "isolated follicular keratosis", "warty dyskeratoma (diagnosis)", "Isolated Follicular Keratosis", "Isolated keratosis follicularis", "Dyskeratosis follicularis, isolated", "Warty dyskeratoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "warty dyskeratoma", "shortest_name_length": 17}
{"curie": "UMLS:C0280953", "names": ["Urinary tract toxicity", "Urinary Tract Toxicity", "urinary tract toxicity", "toxicity, urinary tract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urinary tract toxicity", "shortest_name_length": 22}
{"curie": "UMLS:C2609073", "names": ["Splenic peliosis", "Peliosis of spleen", "Peliosis of spleen (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peliosis of spleen", "shortest_name_length": 16}
{"curie": "MONDO:0019488", "names": ["myoclonic status in non-progressive encephalopathies", "myoclonic epilepsy in non-progressive encephalopathies", "myoclonus epilepsy in non-progressive encephalopathies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myoclonic epilepsy in non-progressive encephalopathies", "shortest_name_length": 52}
{"curie": "MONDO:0005902", "names": ["peanut allergy", "allergy peanut", "Peanut Allergy", "Peanut allergy", "peanuts allergy", "allergy peanuts", "Allergy, Peanut", "peanut allergies", "Peanut Allergies", "allergies peanut", "Allergy to peanut", "Allergies, Peanut", "allergies peanuts", "Allergy to peanuts", "allergy to peanuts", "peanut food allergy", "food allergy peanut", "allergies food peanut", "FOOD ALLERGY TO PEANUT", "Peanut Hypersensitivity", "Hypersensitivity, Peanut", "peanut allergic reaction", "Groundnut Hypersensitivity", "Hypersensitivity, Groundnut", "Allergy to peanut (finding)", "allergy to peanuts (history)", "pigmented ciliary epithelial cell nut allergic reaction", "nut allergic reaction of pigmented ciliary epithelial cell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peanut allergic reaction", "shortest_name_length": 14}
{"curie": "UMLS:C0007621", "names": ["Oncogenesis", "tumorigenesis", "Tumorigenesis", "neoplastic transformation", "neoplastic transformations", "Tumorigenic Transformation", "Tumorigenic Transformations", "Transformation, Tumorigenic", "Transformations, Tumorigenic", "Cell Neoplastic Transformation", "neoplastic cell transformation", "Neoplastic Cell Transformation", "Neoplastic Transformation, Cell", "Cell Neoplastic Transformations", "Transformation, Neoplastic Cell", "Transformation, Cell Neoplastic", "Cell Transformation, Neoplastic", "Neoplastic Cell Transformations", "Transformations, Neoplastic Cell", "Transformations, Cell Neoplastic", "Neoplastic Transformations, Cell", "Cell Transformations, Neoplastic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplastic Cell Transformation", "shortest_name_length": 11}
{"curie": "MONDO:0008707", "names": ["ARUMS", "acrorenal mandibular syndrome", "Acrorenal-Mandibular Syndrome", "acrorenal-mandibular syndrome", "Acrorenal mandibular syndrome", "ACRORENAL-MANDIBULAR SYNDROME", "Acro-renal-mandibular syndrome", "acro-renal-mandibular syndrome", "Acrorenal-Uterine-Mandibular Syndrome", "acrorenal-uterine-mandibular syndrome", "ACRORENAL-UTERINE-MANDIBULAR SYNDROME", "Acro-renal-uterine-mandibular syndrome", "acro-renal-uterine-mandibular syndrome", "Acrorenal mandibular syndrome (disorder)", "split hand split foot mandibular hypoplasia", "Split-Hand And Split-Foot With Mandibular Hypoplasia", "Split hand/split foot-mandibular hypoplasia syndrome", "Split hand and split foot with mandibular hypoplasia", "SPLIT-HAND AND SPLIT-FOOT WITH MANDIBULAR HYPOPLASIA", "split-hand and split-foot with mandibular hypoplasia", "split hand/split foot-mandibular hypoplasia syndrome", "Split hand and split foot with mandibular hypoplasia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acro-renal-mandibular syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0001782", "names": ["Total cataract", "Mature cataract", "mature cataract", "Cataract, total", "cataract mature", "Cataract, mature", "Complete cataract", "Cataract, complete", "total senile cataract", "total or mature cataract", "Total or mature cataract", "Mature cataract (disorder)", "mature cataract (diagnosis)", "Total, mature senile cataract", "total, mature senile cataract", "total senile cataract (diagnosis)", "mature cataract (physical finding)", "Total, mature senile cataract (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mature cataract", "shortest_name_length": 14}
{"curie": "MONDO:0005467", "names": ["Work-related stress disorder", "Work-related stress disorder, NOS", "occupation-related stress disorder", "Occupation-related stress disorder", "Occupation-related stress disorder, NOS", "Occupation-related stress disorder (disorder)", "occupation-related stress disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "occupation-related stress disorder", "shortest_name_length": 28}
{"curie": "UMLS:C1735630", "names": ["Acute cholestatic hepatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute cholestatic hepatitis", "shortest_name_length": 27}
{"curie": "MONDO:0019502", "names": ["AR-NSID", "NS-ARID", "autosomal recessive mental retardation", "mental retardation, autosomal recessive", "autosomal recessive intellectual disability", "intellectual disability, autosomal recessive", "autosomal recessive non-syndromic mental retardation", "autosomal recessive intellectual developmental disorder", "autosomal recessive non-syndromic intellectual disability", "non-syndromic intellectual disability, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive non-syndromic intellectual disability", "shortest_name_length": 7}
{"curie": "MONDO:0022795", "names": ["coenzyme Q cytochrome c reductase deficiency of", "deficiency of coenzyme q cytochrome c reductase"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deficiency of coenzyme q cytochrome c reductase", "shortest_name_length": 47}
{"curie": "MONDO:0007610", "names": ["HTC3", "CGHT", "MICRODELETION 17q24.2-q24.3 SYNDROME", "Microdeletion 17q24.2-q24.3 Syndrome", "microdeletion 17Q24.2-q24.3 syndrome", "microduplication 17Q24.2-q24.3 syndrome", "MICRODUPLICATION 17q24.2-q24.3 SYNDROME", "gingival fibromatosis with hypertrichosis", "Chromosome 17q24.2-q24.3 Deletion Syndrome", "CHROMOSOME 17q24.2-q24.3 DELETION SYNDROME", "chromosome 17Q24.2-q24.3 deletion syndrome", "Fibromatosis, Gingival, with Hypertrichosis", "FIBROMATOSIS, GINGIVAL, WITH HYPERTRICHOSIS", "fibromatosis, gingival, with hypertrichosis", "extreme hirsutism with gingival fibromatosis", "CHROMOSOME 17q24.2-q24.3 DUPLICATION SYNDROME", "chromosome 17Q24.2-q24.3 Duplication syndrome", "gingival fibromatosis-hypertrichosis syndrome", "Gingival fibromatosis-hypertrichosis syndrome", "congenital generalized hypertrichosis terminalis", "Congenital generalized hypertrichosis terminalis", "Gingival fibromatosis and hypertrichosis syndrome", "Hirsutism-congenital gingival hyperplasia syndrome", "Hirsutism congenital gingival hyperplasia syndrome", "hirsutism-congenital gingival hyperplasia syndrome", "hypertrichosis with or without gingival hyperplasia", "Hypertrichosis with or without gingival hyperplasia", "hereditary gingival fibromatosis with hypertrichosis", "Gingival fibromatosis and hypertrichosis syndrome (disorder)", "hypertrichosis terminalis, generalized, with gingival hyperplasia", "hypertrichosis, congenital generalized, with gingival hyperplasia", "Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia", "HYPERTRICHOSIS, CONGENITAL GENERALIZED, WITH OR WITHOUT GINGIVAL HYPERPLASIA", "hypertrichosis terminalis, generalized, with or without gingival hyperplasia", "hypertrichosis, congenital generalized, with or without gingival hyperplasia", "HYPERTRICHOSIS TERMINALIS, GENERALIZED, WITH OR WITHOUT GINGIVAL HYPERPLASIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gingival fibromatosis-hypertrichosis syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0235333", "names": ["chemical esophagitis", "Esophagitis chemical", "Chemical Esophagitis", "ESOPHAGITIS CHEMICAL", "Chemical esophagitis", "Oesophagitis chemical", "Corrosive esophagitis", "Chemical oesophagitis", "chemical oesophagitis", "corrosive esophagitis", "OESOPHAGITIS CHEMICAL", "Corrosive oesophagitis", "Chemical esophagitis (disorder)", "chemical esophagitis (diagnosis)", "corrosive esophagitis (diagnosis)", "Esophagitis due to Corrosive Agent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chemical esophagitis", "shortest_name_length": 20}
{"curie": "MONDO:0007604", "names": ["FFS", "FHUFS", "Femoral-facial syndrome", "femoral-facial syndrome", "Femoral facial syndrome", "femoral facial syndrome", "Femoral-Facial Syndrome", "FEMORAL-FACIAL SYNDROME", "femoral dysgenesis, bilateral", "femoral hypoplasia-unusual facies syndrome", "Femoral Hypoplasia-Unusual Facies Syndrome", "Femoral hypoplasia unusual facies syndrome", "femoral hypoplasia unusual facies syndrome", "Femoral hypoplasia-unusual facies syndrome", "FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME", "Femoral dysgenesis, bilateral-Robin anomaly", "Femoral hypoplasia - unusual facies syndrome", "Femoral hypoplasia - unusual facies syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "femoral-facial syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C1699738", "names": ["intraoperative endocrine injury", "Intraoperative Endocrine Injury", "Intraoperative endocrine injury", "intraoperative endocrine injury (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraoperative Endocrine Injury", "shortest_name_length": 31}
{"curie": "UMLS:C0494165", "names": ["liver metastasis", "Liver metastases", "liver metastases", "Liver Metastases", "LIVER METASTASIS", "Liver Metastasis", "Liver metastasis", "Liver secondaries", "liver secondaries", "Hepatic metastasis", "HEPATIC METASTASES", "hepatic metastases", "Hepatic metastases", "hepatic metastasis", "metastasis to liver", "Metastasis to liver", "Metastases to liver", "metastases to liver", "Liver secondary cancer", "secondary liver cancer", "metastatic liver cancer", "Metastases to liver, NOS", "LIVER CANCER, METASTATIC", "secondary cancer of liver", "Cancer metastatic to liver", "metastatic cancer to liver", "HEPATIC NEOPLASM SECONDARY", "Cancer of liver, secondary", "cancer, metastatic to liver", "liver, metastatic cancer to", "Metastatic neoplasm of liver", "Secondary malignancy of liver", "Metastatic Tumor to the Liver", "Metastatic Neoplasm to the Liver", "secondary malignant neoplasm liver", "Secondary malignant neoplasm of liver", "Metastatic malignant neoplasm of liver", "Malignant neoplasm of liver, secondary", "Metastatic malignant neoplasm to liver", "metastasis of malignant neoplasm to liver", "Secondary malignant neoplasm of liver, NOS", "Metastatic Malignant Neoplasm in the Liver", "Metastatic Malignant Neoplasm to the Liver", "Metastatic malignant neoplasm to liver, NOS", "Metastatic malignant neoplasm to liver (disorder)", "Secondary malignant neoplasm of liver (diagnosis)", "Malignant neoplasm of liver, specified as secondary", "metastasis of malignant neoplasm to liver (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to liver", "shortest_name_length": 16}
{"curie": "MONDO:0030781", "names": ["RSDM2", "restrictive dermopathy 2", "RESTRICTIVE DERMOPATHY 2", "RESTRICTIVE DERMOPATHY 2, LETHAL", "restrictive dermopathy 2, lethal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "restrictive dermopathy 2", "shortest_name_length": 5}
{"curie": "UMLS:C0019250", "names": ["Hereditary hypofibrinogenemia", "Hereditary Factor I Deficiency", "Hereditary hypofibrinogenaemia", "Hereditary factor I deficiency disease", "Hereditary factor I deficiency disease, NOS", "Hereditary factor I deficiency disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hereditary factor I deficiency disease", "shortest_name_length": 29}
{"curie": "MONDO:0020596", "names": ["Mucin-Producing Carcinoma", "Mucin-producing carcinoma", "mucin-producing carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucin-producing carcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0800029", "names": ["uip", "IPF", "UIP", "CFA", "ILD2", "hamman rich disease", "hamman-rich disease", "Hamman-Rich disease", "Hamman-Rich Disease", "HAMMAN-RICH DISEASE", "Hamman-rich disease", "Fibrosing alveolitis", "fibrosing alveolitis", "disease hammans rich", "Alveolitis fibrosing", "ALVEOLITIS FIBROSING", "ALVEOLITIS, FIBROSING", "fibrosing; alveolitis", "alveolitis; fibrosing", "lung; fibrosis, idiopathic", "Carrington-Liebow syndrome", "fibrosis; lung, idiopathic", "INTERSTITIAL LUNG DISEASE 2", "interstitial lung disease 2", "Usual Interstitial Pneumonia", "diopathic pulmonary fibrosis", "Usual interstitial pneumonia", "usual interstitial pneumonia", "fibrosis idiopathic pulmonary", "pulmonary fibrosis idiopathic", "Idiopathic Pulmonary Fibroses", "Idiopathic Pulmonary Fibrosis", "Idiopathic pulmonary fibrosis", "idiopathic pulmonary fibrosis", "Interstitial Pneumonia, Usual", "Usual Interstitial Pneumonias", "PULMONARY FIBROSIS IDIOPATHIC", "FIBROSIS, IDIOPATHIC PULMONARY", "Usual interstitial pneumonitis", "pulmonary fibrosis, idiopathic", "Pulmonary Fibrosis, Idiopathic", "usual interstitial pneumonitis", "Pulmonary Fibroses, Idiopathic", "Usual Interstitial Pneumonitis", "PULMONARY FIBROSIS, IDIOPATHIC", "PNEUMONITIS, USUAL INTERSTITIAL", "interstitial pneumonitis, usual", "FIBROCYSTIC PULMONARY DYSPLASIA", "Pneumonitis, Usual Interstitial", "Interstitial Pneumonitis, Usual", "fibrocystic pulmonary dysplasia", "Fibrocystic Pulmonary Dysplasia", "Idiopathic fibrosing alveolitis", "INTERSTITIAL PNEUMONITIS, USUAL", "Dysplasia, Fibrocystic Pulmonary", "Cryptogenic Fibrosing Alveolitis", "Usual Interstitial Pneumonitides", "Cryptogenic fibrosing alveolitis", "cryptogenic fibrosing alveolitis", "Fibrocystic Pulmonary Dysplasias", "Pulmonary Dysplasia, Fibrocystic", "Fibrosing alveolitis (idiopathic)", "fibrosis idiopathic ipf pulmonary", "Fibrosing Alveolitis, Cryptogenic", "FIBROSING ALVEOLITIS, CRYPTOGENIC", "Pneumonitides, Usual Interstitial", "fibrosing alveolitis, cryptogenic", "Cryptogenic Fibrosing Alveolitides", "IPF - Idiopathic pulmonary fibrosis", "IPF - idiopathic pulmonary fibrosis", "Fibrosing Alveolitides, Cryptogenic", "UIP - Usual interstitial pneumonitis", "ALVEOLITIS, CHRONIC DIFFUSE FIBROSING", "Familial Idiopathic Pulmonary Fibrosis", "familial idiopathic pulmonary fibrosis", "CFA - Cryptogenic fibrosing alveolitis", "ALVEOLITIS, CHRONIC DIFFUSE SCLEROSING", "Familial idiopathic pulmonary fibrosis", "pulmonary fibrosis idiopathic familial", "Idiopathic Pulmonary Fibrosis, Familial", "idiopathic pulmonary fibrosis, familial", "diffuse interstitial pulmonary fibrosis", "IDIOPATHIC PULMONARY FIBROSIS, FAMILIAL", "usual interstitial pneumonia (diagnosis)", "Idiopathic pulmonary fibrosis (disorder)", "idiopathic pulmonary fibrosis (diagnosis)", "cryptogenic fibrosing alveolitis (diagnosis)", "Idiopathic Fibrosing Alveolitis, Chronic Form", "Idiopathic fibrosing alveolitis, chronic form", "usual interstitial pneumonia (Carrington-Liebow)", "Familial idiopathic pulmonary fibrosis (disorder)", "Familial idiopathic pulmonary fibrosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "interstitial lung disease 2", "shortest_name_length": 3}
{"curie": "MONDO:0002588", "names": ["Thymoma Type A", "thymoma type A", "type A thymoma", "Thymoma type A", "Medullary Thymoma", "medullary thymoma", "Thymoma, medullary", "thymoma, medullary", "Spindle Cell Thymoma", "spindle cell thymoma", "Thymoma type A (disorder)", "type A thymoma (diagnosis)", "Primary thymic epithelial tumor type A", "primary thymic epithelial tumor type A", "Primary thymic epithelial neoplasm type A", "primary thymic epithelial neoplasm type A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thymoma type A", "shortest_name_length": 14}
{"curie": "MONDO:0019661", "names": ["Pfeiffer syndrome type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pfeiffer syndrome type 3", "shortest_name_length": 24}
{"curie": "UMLS:C1335314", "names": ["Pancreatic Premalignant Condition", "Pancreatic Precancerous Condition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Precancerous Condition", "shortest_name_length": 33}
{"curie": "MONDO:0020246", "names": ["Vitreoretinopathy", "Vitreoretinal abnormality", "Vitreoretinal degeneration", "inherited vitreoretinopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited vitreoretinopathy", "shortest_name_length": 17}
{"curie": "MONDO:0001770", "names": ["Gastrin secretion disorder", "abnormal; gastrin secretion", "gastrin; secretion abnormal", "secretion; gastrin abnormal", "gastrin secretion abnormality", "Abnormal secretion of gastrin", "Gastrin secretion disorder NOS", "Abnormality of gastrin secretion", "Abnormality of secretion of gastrin", "Abnormality of secretion of gastrin (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastrin secretion abnormality", "shortest_name_length": 26}
{"curie": "UMLS:C5206823", "names": ["Unresectable Merkel Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Merkel Cell Carcinoma", "shortest_name_length": 34}
{"curie": "UMLS:C1332971", "names": ["Childhood Liver Neoplasm", "Childhood Hepatic Neoplasm", "Childhood Liver and Intrahepatic Bile Duct Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Liver and Intrahepatic Bile Duct Neoplasm", "shortest_name_length": 24}
{"curie": "MONDO:0014934", "names": ["SCAR24", "UBA5 autosomal dominant cerebellar ataxia", "autosomal recessive spinocerebellar ataxia 24", "spinocerebellar ataxia, autosomal recessive 24", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 24", "spinocerebellar ataxia, autosomal recessive type 24", "spinocerebellar ataxia, autosomal recessive 24; SCAR24", "autosomal dominant cerebellar ataxia caused by mutation in UBA5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia, autosomal recessive 24", "shortest_name_length": 6}
{"curie": "MONDO:0022174", "names": ["12p-", "12p del", "del(12p)", "12p monosomy", "deletion 12p", "monosomy 12p", "Deletion 12p", "Monosomy 12p", "12p deletion", "12p- syndrome", "del(12p) syndrome", "partial monosomy 12p", "deletion 12p syndrome", "12p deletion syndrome", "12p monosomy, partial", "loss of chromosome 12p", "Loss of Chromosome 12p", "Chromosome 12p deletion", "chromosome 12p monosomy", "chromosome 12p deletion", "Chromosome 12p partial deletion", "chromosome 12p deletion syndrome", "partial deletion of chromosome 12p", "Partial monosomy of chromosome 12p", "Partial deletion of chromosome 12p", "partial monosomy of chromosome 12p", "partial deletion of the short arm of chromosome 12", "Partial monosomy of the short arm of chromosome 12", "partial monosomy of the short arm of chromosome 12", "Partial deletion of the short arm of chromosome 12", "partial deletion of the short arm of chromosome type 12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 12p deletion", "shortest_name_length": 4}
{"curie": "MONDO:0017648", "names": ["chorea minor", "Chorea Minor", "acute chorea", "minor; chorea", "CHOREA, MINOR", "CHOREA, ACUTE", "chorea; minor", "dance st vitus", "Sydenham chorea", "sydenham chorea", "St. Vitus Dance", "SYDENHAM CHOREA", "Sydenham Chorea", "Sydenham; chorea", "dance st vitus's", "Sydenhams chorea", "chorea sydenhams", "Chorea, Sydenham", "sydenhams chorea", "Sydenham Choreas", "Chorea;Sydenhams", "Chorea;rheumatic", "rheumatic chorea", "St. Vitus' dance", "Rheumatic Chorea", "Rheumatic chorea", "Sydenhams Chorea", "st. vitus' dance", "St. Vitus' Dance", "chorea; Sydenham", "SYDENHAMS CHOREA", "St. Vituss Dance", "st. vitus's dance", "St. Vitus's Dance", "Chorea, Rheumatic", "rheumatic; chorea", "Choreas, Sydenham", "sydenham's chorea", "SAINT VITUS DANCE", "chorea; rheumatic", "saint vitus dance", "Rheumatic Choreas", "Sydenham's chorea", "vitus dance saint", "Sydenham's Chorea", "St. Vitus's Dances", "Chorea, Sydenham's", "Choreas, Rheumatic", "Rheumatic chorea NOS", "Rheumatic chorea (disorder)", "Sydenham's chorea (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sydenham chorea", "shortest_name_length": 12}
{"curie": "MONDO:0041879", "names": ["Staphylococcus aureus pneumonia", "staphylococcus aureus pneumonia", "Staphylococcus aureus caused pneumonia", "pneumonia due to staphylococcus aureus", "Pneumonia due to staphylococcus aureus", "Pneumonia due to Staphylococcus aureus", "Pneumonia caused by Staphylococcus aureus", "pneumonia caused by staphylococcus aureus", "Pneumonia due to Staphylococcus aureus NOS", "Pneumonia caused by Staphylococcus aureus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "staphylococcus aureus pneumonia", "shortest_name_length": 31}
{"curie": "MONDO:0018672", "names": ["IgG4-related aortitis", "IgG4-related periaortitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IgG4-related aortitis", "shortest_name_length": 21}
{"curie": "MONDO:0022656", "names": ["cardiomyopathy spherocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiomyopathy spherocytosis", "shortest_name_length": 28}
{"curie": "MONDO:0020517", "names": ["Eosinophilic Granuloma", "Eosinophilic granuloma", "granuloma eosinophilic", "EOSINOPHILIC GRANULOMA", "eosinophilic granuloma", "eosinophilic; granuloma", "granuloma; eosinophilic", "Granuloma, Eosinophilic", "Eosinophilic Granulomas", "Granulomas, Eosinophilic", "unifocal eosinophilic granuloma", "Eosinophilic granuloma (disorder)", "eosinophilic granuloma (diagnosis)", "Eosinophilic xanthomatous granuloma", "Eosinophilic Xanthomatous Granuloma", "eosinophilic xanthomatous granuloma", "Unifocal Langerhans-cell histiocytosis", "unifocal Langerhans cell histiocytosis", "Unifocal Langerhans Cell Histiocytosis", "Langerhans cell histiocytosis, unifocal", "Monostotic Langerhans cell histiocytosis", "Langerhans cell granulomatosis, unifocal", "Monostotic Langerhans Cell Histiocytosis", "Langerhans Cell Histiocytosis, Monostotic", "Mono-ostotic Langerhans cell histiocytosis", "Langerhans cell histiocytosis, mono-ostotic", "chronic unifocal Langerhans cell histiocytosis", "Chronic Unifocal Langerhans Cell Histiocytosis", "histiocytoses, unifocal eosinophilic granuloma", "Eosinophilic granuloma (morphologic abnormality)", "Langerhans cell histiocytosis, unifocal (clinical)", "chronic and localized Langerhans cell histiocytosis", "histiocytoses, unifocal eosinophilic granuloma (diagnosis)", "Monostotic Langerhans cell histiocytosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eosinophilic granuloma", "shortest_name_length": 22}
{"curie": "MONDO:0003786", "names": ["childhood choriocarcinoma of testis", "Childhood Choriocarcinoma of Testis", "pediatric choriocarcinoma of testis", "Pediatric Choriocarcinoma of Testis", "pediatric testicular Choriocarcinoma", "Pediatric Testicular Choriocarcinoma", "pediatric testicular choriocarcinoma", "childhood testicular choriocarcinoma", "Childhood Testicular Choriocarcinoma", "choriocarcinoma of testis of childhood", "childhood choriocarcinoma of the testis", "pediatric choriocarcinoma of the testis", "Childhood Choriocarcinoma of the Testis", "Pediatric Choriocarcinoma of the Testis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood testicular choriocarcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C5418921", "names": ["Advanced Glioblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Glioblastoma", "shortest_name_length": 21}
{"curie": "MONDO:0013072", "names": ["EDMD5", "autosomal dominant Emery-Dreifuss muscular dystrophy 5", "EMERY-Dreifuss muscular dystrophy 5, autosomal dominant", "EMERY-DREIFUSS MUSCULAR DYSTROPHY 5, AUTOSOMAL DOMINANT", "Emery-Dreifuss muscular dystrophy 5, autosomal dominant", "SYNE2 autosomal dominant Emery-Dreifuss muscular dystrophy", "autosomal dominant Emery-Dreifuss muscular dystrophy caused by mutation in SYNE2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Emery-Dreifuss muscular dystrophy 5, autosomal dominant", "shortest_name_length": 5}
{"curie": "MONDO:0016522", "names": ["Kousseff syndrome", "Sacral meningocele conotruncal heart defects", "sacral meningocele conotruncal heart defects", "Sacral meningocele-conotruncal heart defects syndrome", "sacral meningocele-conotruncal heart defects syndrome", "Congenital sacral meningocele with conotruncal heart defect syndrome", "Congenital sacral meningocoele with conotruncal heart defect syndrome", "Congenital sacral meningocele with conotruncal heart defect syndrome (disorder)", "sacral meningocele, conotruncal heart defects, and minor anomalies of head and neck"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kousseff syndrome", "shortest_name_length": 17}
{"curie": "UMLS:C5243641", "names": ["Immune-mediated cholangitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immune-mediated cholangitis", "shortest_name_length": 27}
{"curie": "UMLS:C4053952", "names": ["Systemic Lupus Erythematosus Nephritis Class V"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Systemic Lupus Erythematosus Nephritis Class V", "shortest_name_length": 46}
{"curie": "MONDO:0005528", "names": ["vitamin metabolic disorder", "inborn vitamin metabolic disorder", "inborn error of vitamin metabolic process", "inborn vitamin metabolic process disorder", "rare inborn error of vitamin metabolic process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn vitamin metabolic disorder", "shortest_name_length": 26}
{"curie": "UMLS:C3899844", "names": ["C4 Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "C4 Deficiency", "shortest_name_length": 13}
{"curie": "MONDO:0013730", "names": ["GVH", "gvh", "gvhd", "GvHD", "GVHD", "gvh disease", "GVH disease", "runt disease", "Runt Disease", "Runt disease", "disease, runt", "Disease, Runt", "Runting syndrome", "graft-vs-host disease", "Graft vs Host Disease", "disease graft host vs", "Graft-vs-Host Disease", "Graft-vs-Host disease", "host vs graft disease", "graft vs host disease", "graft vs. host disease", "Disease, Graft-vs-Host", "graft-VS-host diseases", "disease, graft-vs-host", "Graft-vs-Host Diseases", "Graft Vs. Host Disease", "Diseases, Graft-vs-Host", "diseases, graft-vs-host", "Graft-versus-host disease", "disease graft host versus", "graft-versus-host-disease", "graft-versus-host disease", "disease graft versus host", "Graft-Versus-Host-Disease", "graft versus host disease", "Graft-Versus-Host Disease", "Graft versus host disease", "Graft Versus Host Disease", "host versus graft disease", "GRAFT VERSUS HOST DISEASE", "homologous wasting disease", "Graft Versus Host Diseases", "Graft-Versus-Host Diseases", "disease, graft-versus-host", "Disease, Graft-Versus-Host", "Homologous Wasting Disease", "graft-versus-host diseases", "disease, homologous wasting", "Disease, Homologous Wasting", "Diseases, Graft-Versus-Host", "diseases, graft-versus-host", "Graft versus host disease, NOS", "GVHD - Graft-versus-host disease", "GVHD (graft-versus-host disease)", "Graft-versus-host disease (disorder)", "autoimmune foreign transplant disease", "graft-versus-host disease (diagnosis)", "Graft-versus-host disease, unspecified", "graft-versus-host disease, resistance to", "graft-versus-host disease, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "graft versus host disease", "shortest_name_length": 3}
{"curie": "UMLS:C0220612", "names": ["childhood NHL", "Childhood NHL", "pediatric NHL", "NHL, childhood", "Non-Hodgkin Lymphoma", "Non-Hodgkin lymphoma, child", "Childhood Non-Hodgkin Lymphoma", "Pediatric Non-Hodgkin Lymphoma", "childhood non-Hodgkin lymphoma", "Pediatric Non-Hodgkin's Lymphoma", "pediatric non-Hodgkin's lymphoma", "Childhood Non-Hodgkin's Lymphoma", "childhood non-Hodgkin's lymphoma", "non-Hodgkin's lymphoma, childhood", "lymphoma, non-Hodgkin's, childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Non-Hodgkin Lymphoma", "shortest_name_length": 13}
{"curie": "MONDO:0023019", "names": ["dwarfism bluish sclerae"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dwarfism bluish sclerae", "shortest_name_length": 23}
{"curie": "UMLS:C5420283", "names": ["Head and Neck Heterotopia-Associated Carcinoma", "Head and Neck Accessory Tissue-Associated Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Head and Neck Heterotopia-Associated Carcinoma", "shortest_name_length": 46}
{"curie": "MONDO:0003299", "names": ["Colorectal Leiomyoma", "colorectum leiomyoma", "colorectal leiomyoma", "large bowel leiomyoma", "Large Bowel Leiomyoma", "leiomyoma of large bowel", "Leiomyoma of Large Bowel", "Large Intestine Leiomyoma", "large intestine leiomyoma", "leiomyoma of large Intestine", "leiomyoma of large intestine", "leiomyoma of the large bowel", "Leiomyoma of Large Intestine", "Leiomyoma of the Large Bowel", "Leiomyoma of large intestine", "leiomyoma of the large intestine", "Leiomyoma of the Large Intestine", "Leiomyoma of large intestine (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorectal leiomyoma", "shortest_name_length": 20}
{"curie": "UMLS:C4521754", "names": ["Stage III Gastric (Stomach) Cancer", "Clinical Stage III Gastric Cancer AJCC v8", "Clinical Stage III Gastric Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage III Gastric Cancer AJCC v8", "shortest_name_length": 34}
{"curie": "UMLS:C5239046", "names": ["High Risk Acute Lymphoblastic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Risk Acute Lymphoblastic Leukemia", "shortest_name_length": 38}
{"curie": "MONDO:0009507", "names": ["Lambert syndrome", "LAMBERT SYNDROME", "branchial dysplasia clubfoot inguinal hernia and biliary atresia", "BRANCHIAL DYSPLASIA, CLUBFOOT, INGUINAL HERNIA, AND BILIARY ATRESIA", "Branchial dysplasia, clubfoot, inguinal hernia, and biliary atresia", "branchial dysplasia, clubfoot, inguinal hernia, and biliary atresia", "Branchial dysplasia-intellectual disability-inguinal hernia syndrome", "branchial dysplasia-intellectual disability-inguinal hernia syndrome", "Branchial dysplasia, intellectual disability, inguinal hernia syndrome", "branchial dysplasia, intellectual disability, inguinal hernia syndrome", "Branchial dysplasia, intellectual disability, inguinal hernia syndrome (disorder)", "branchial dysplasia, intellectual disability, inguinal hernia syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lambert syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0019627", "names": ["Isolated congenital alacrima", "isolated congenital alacrima", "nonsyndromic congenital alacrima", "Isolated congenital alacrima (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated congenital alacrima", "shortest_name_length": 28}
{"curie": "UMLS:C3282876", "names": ["Aleukemic lymphocytic leukemia", "Aleukemic Lymphocytic Leukemia", "Aleukemic Chronic Lymphocytic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aleukemic Chronic Lymphocytic Leukemia", "shortest_name_length": 30}
{"curie": "UMLS:C4525207", "names": ["IVA", "Stage IVA Hepatocellular Cancer", "Stage IVA Liver Cell Carcinoma AJCC v8", "Stage IVA Hepatocellular Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Hepatocellular Carcinoma AJCC v8", "shortest_name_length": 3}
{"curie": "MONDO:0054550", "names": ["ANFH", "ANFH1", "OSTEONECROSIS OF FEMORAL HEAD", "osteonecrosis of femoral head", "Avascular necrosis femoral head", "avascular necrosis femoral head", "avascular femoral head necrosis", "femoral head avascular necrosis", "FEMORAL HEAD NECROSIS AVASCULAR", "AVASCULAR NECROSIS FEMORAL HEAD", "Avascular Necrosis of Femur Head", "avascular femoral heads necrosis", "ISCHEMIC NECROSIS OF FEMORAL HEAD", "femoral head, aseptic necrosis of", "ischemic necrosis of femoral head", "FEMORAL HEAD, ASEPTIC NECROSIS OF", "Ischemic Necrosis Of Femoral Head", "Avascular necrosis of femoral head", "Necrosis, Avascular, of Femur Head", "Avascular Necrosis of Femoral Head", "Femoral head, avascular necrosis of", "Femoral Head, Avascular Necrosis Of", "FEMORAL HEAD, AVASCULAR NECROSIS OF", "avascular necrosis of the femoral head", "Avascular necrosis of the femoral head", "Avascular necrosis of the head of femur", "Avascular Necrosis Of Femoral Head, Primary", "AVASCULAR NECROSIS OF FEMORAL HEAD, PRIMARY, 1", "avascular necrosis of femoral head, primary, 1", "AVASCULAR NECROSIS OF THE FEMORAL HEAD, PRIMARY, 1", "Avascular necrosis of the head of femur (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "avascular necrosis of femoral head, primary, 1", "shortest_name_length": 4}
{"curie": "MONDO:0023691", "names": ["MSUD type 1A", "maple syrup urine disease type 1A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maple syrup urine disease type 1A", "shortest_name_length": 12}
{"curie": "MONDO:0035534", "names": ["DONSON-related microcephaly-short stature-limb abnormalities spectrum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DONSON-related microcephaly-short stature-limb abnormalities spectrum", "shortest_name_length": 69}
{"curie": "UMLS:C0278686", "names": ["stage II ovary cancer", "ovary cancer, stage II", "stage II ovarian cancer", "Ovarian cancer stage II", "Ovarian Cancer Stage II", "Stage II Ovarian Cancer", "ovarian cancer, stage II", "Stage II Ovarian Carcinoma", "stage II ovarian carcinoma", "ovarian carcinoma, stage II", "FIGO Stage II Ovarian Cancer", "AJCC Stage II Ovarian Cancer", "FIGO Stage II Cancer of Ovary", "Stage II Ovarian Cancer AJCC v6", "FIGO Stage II Ovarian Carcinoma", "Stage II Ovarian Cancer AJCC v7", "FIGO Stage II Carcinoma of Ovary", "FIGO Stage II Cancer of the Ovary", "Ovarian epithelial cancer stage II", "stage II ovarian epithelial cancer", "Stage II Ovarian Epithelial Cancer", "ovarian epithelial cancer, stage II", "FIGO Stage II Carcinoma of the Ovary", "Stage II Ovarian Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian epithelial cancer stage II", "shortest_name_length": 21}
{"curie": "UMLS:C1882075", "names": ["Neutrophil Actin Defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neutrophil Actin Defect", "shortest_name_length": 23}
{"curie": "MONDO:0019364", "names": ["Pseudotyphus of California", "pseudotyphus of California", "Infection caused by Rickettsia felis", "Infection caused by Rickettsia felis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudotyphus of California", "shortest_name_length": 26}
{"curie": "UMLS:C0151730", "names": ["DRUG EFFECT INCREASED", "Increased drug effect", "Drug action increased", "INCREASED DRUG EFFECT", "Drug effect increased", "Drug action increased (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drug action increased", "shortest_name_length": 21}
{"curie": "MONDO:0024335", "names": ["Neuritis retrobulbar", "RETROBULBAR NEURITIS", "retrobulbar neuritis", "neuritis retrobulbar", "NEURITIS RETROBULBAR", "Retrobulbar Neuritis", "Retrobulbar neuritis", "Neuritis, Retrobulbar", "Retro-bulbar neuritis", "Retrobulbar Neuritides", "Neuritides, Retrobulbar", "Posterior Optic Neuritis", "Retrobulbar neuritis NOS", "Optic Neuritis, Posterior", "Neuritis, Posterior Optic", "RBN - Retrobulbar neuritis", "Retrobulbar optic neuritis", "Posterior Optic Neuritides", "retrobulbar optic neuritis", "Optic neuritis retrobulbar", "optic neuritis retrobulbar", "Optic Neuritides, Posterior", "Neuritides, Posterior Optic", "optic; neuritis, retrobulbar", "neuritis; optic, retrobulbar", "Retrobulbar neuritis (disorder)", "retrobulbar neuritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retrobulbar neuritis", "shortest_name_length": 20}
{"curie": "MONDO:0004189", "names": ["esophagus tuberculosis", "esophageal tuberculosis", "Esophageal tuberculosis", "Oesophageal tuberculosis", "Tuberculosis of esophagus", "tuberculosis of esophagus", "Tuberculosis of oesophagus", "Tuberculosis of esophagus (disorder)", "tuberculosis of esophagus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophageal tuberculosis", "shortest_name_length": 22}
{"curie": "UMLS:C4526607", "names": ["Stage I Thymoma", "Stage I Thymoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Thymoma AJCC v8", "shortest_name_length": 15}
{"curie": "UMLS:C4728124", "names": ["Gastrointestinal scarring"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal scarring", "shortest_name_length": 25}
{"curie": "UMLS:C4324413", "names": ["Fetal renal impairment", "Foetal renal impairment"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fetal renal impairment", "shortest_name_length": 22}
{"curie": "UMLS:C0347869", "names": ["Akinetic seizures", "seizure; akinetic", "akinetic epilepsy", "Akinetic Epilepsy", "Seizures, akinetic", "epilepsy; akinetic", "akinetic; seizures", "Epilepsy, Akinetic", "Akinetic Epilepsies", "akinetic; epileptic", "Epilepsies, Akinetic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epilepsy, Akinetic", "shortest_name_length": 17}
{"curie": "UMLS:C0347001", "names": ["prostate metastasis", "prostate metastases", "Metastasis to Prostate", "Metastases to Prostate", "Metastases to prostate", "Metastasis to prostate", "Metastases to the Prostate", "Metastasis to the Prostate", "Metastatic tumor to prostate", "Metastatic tumour to prostate", "Cancer metastatic to prostate", "Metastatic Tumor to the Prostate", "Metastatic Neoplasm to the Prostate", "Secondary malignant neoplasm of prostate", "secondary malignant neoplasm of prostate", "Metastatic malignant neoplasm to prostate", "Metastatic malignant neoplasm of prostate", "Metastatic Malignant Neoplasm to the Prostate Gland", "Metastatic Malignant Neoplasm in the Prostate Gland", "Metastatic malignant neoplasm to prostate (disorder)", "secondary malignant neoplasm of prostate (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to prostate", "shortest_name_length": 19}
{"curie": "UMLS:C0751782", "names": ["May-White Syndrome", "May White Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "May-White Syndrome", "shortest_name_length": 18}
{"curie": "UMLS:C5243900", "names": ["Pyroglutamic acidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pyroglutamic acidosis", "shortest_name_length": 21}
{"curie": "MONDO:0100195", "names": ["X-linked intellectual disability with hypopituitarism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability with hypopituitarism", "shortest_name_length": 53}
{"curie": "UMLS:C1142347", "names": ["Esophageal adenocarcinoma stage IV", "Oesophageal adenocarcinoma stage IV", "Esophageal adenocarcinoma metastatic", "Metastatic Esophageal Adenocarcinoma", "Oesophageal adenocarcinoma metastatic", "Esophageal adenocarcinoma site unspecified stage IV", "Oesophageal adenocarcinoma site unspecified stage IV"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal adenocarcinoma stage IV", "shortest_name_length": 34}
{"curie": "MONDO:0004373", "names": ["Papillary Meningioma", "papillary meningioma", "adult papillary meningioma", "Adult Papillary Meningioma", "papillary meningioma, adult", "papillary meningioma of adults"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult papillary meningioma", "shortest_name_length": 20}
{"curie": "MONDO:0024575", "names": ["Disease;pregnancy", "pregnancy disease", "pregnancy disorder", "Pregnancy Disorder", "PREGNANCY DISORDER", "Pregnancy disorder", "disease of pregnancy", "Disorder of pregnancy", "Complicated;pregnancy", "Disorder of Pregnancy", "complicates pregnancy", "complicated pregnancy", "PREGNANCY COMPLICATED", "disorder of pregnancy", "pregnancy complication", "Pregnancy complication", "complication pregnancy", "Pregnancy Complication", "Pregnancy, complicated", "complicating pregnancy", "Pregnancy Complications", "complication, pregnancy", "complications pregnancy", "Complication, Pregnancy", "complicated pregnancies", "pregnancy complications", "pregnancy; complications", "Pregnancy--Complications", "Complications, pregnancy", "Complications, Pregnancy", "Complication of pregnancy", "Disease of pregnancy, NOS", "complications pregnancies", "complication of pregnancy", "Complicated pregnancy, NOS", "pregnant with complication", "of pregnancy complications", "complications of pregnancy", "Disorder of pregnancy, NOS", "Pregnancy, Complications of", "Complication of pregnancy NOS", "complications pregnancy related", "Disorder of pregnancy (disorder)", "Complication Related to Pregnancy", "COMPLICATIONS RELATED TO PREGNANCY", "pregnancy complications (diagnosis)", "pregnant with complication (history)", "Unspecified complication of pregnancy", "Complication related to pregnancy, NOS", "complication of pregnancy or childbirth", "disorder of pregnancy, childbirth, or puerperium", "DIAGNOSES RELATED TO PREGNANCY AND THE PERINATAL PERIOD"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pregnancy disorder", "shortest_name_length": 17}
{"curie": "UMLS:C0280179", "names": ["Stage IV Burkitt Lymphoma", "stage IV adult Burkitt lymphoma", "Stage IV Adult Burkitt Lymphoma", "Stage IV Adult Burkitt's Lymphoma", "Ann Arbor Stage IV Adult Burkitt Lymphoma", "adult small noncleaved cell lymphoma, stage IV", "metastatic adult small noncleaved cell lymphoma", "adult small noncleaved cell lymphoma, metastatic", "Stage IV Adult Diffuse Small Non-Cleaved Cell Lymphoma", "Adult Diffuse Small Non-Cleaved Cell Lymphoma Stage IV", "Metastatic Adult Diffuse Small Non-Cleaved Cell Lymphoma", "stage IV adult diffuse small noncleaved cell/Burkitt's lymphoma", "Stage IV Adult Diffuse Small Non-Cleaved Cell/Burkitt's Lymphoma", "Adult Diffuse Small Non-Cleaved Cell/Burkitt's Lymphoma Stage IV", "Metastatic Adult Diffuse Small Non-Cleaved Cell/Burkitt's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Adult Burkitt Lymphoma", "shortest_name_length": 25}
{"curie": "MONDO:0013301", "names": ["AROMATASE DEFICIENCY", "aromatase deficiency", "Aromatase Deficiency", "Aromatase deficiency", "P450-aromatase Deficiency", "P450-Aromatase Deficiency", "congenital estrogen deficiency", "Congenital estrogen deficiency", "Maternal virilization due to placental aromatase deficiency", "Maternal virilisation due to placental aromatase deficiency", "PSEUDOHERMAPHRODITISM, FEMALE, DUE TO PLACENTAL AROMATASE DEFICIENCY", "Pseudohermaphroditism, female, due to placental aromatase deficiency", "pseudohermaphroditism, female, due to placental aromatase deficiency", "Maternal virilization due to placental aromatase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aromatase deficiency", "shortest_name_length": 20}
{"curie": "MONDO:0009016", "names": ["Band Keratopathy", "Band keratopathy", "Keratopathy band", "band keratopathy", "BAND KERATOPATHY", "keratopathy; band", "band; keratopathy", "BK - Band keratopathy", "Band-shaped keratitis", "Band shaped keratopathy", "Band-shaped keratopathy", "band-shaped keratopathy", "Calcific band keratopathy", "band keratopathy (diagnosis)", "Band-shaped corneal dystrophy", "Corneal Dystrophy, Band-Shaped", "CORNEAL DYSTROPHY, BAND-SHAPED", "corneal dystrophy, band-SHAPED", "Band-shaped keratopathy (disorder)", "band keratopathy (physical finding)", "corneal degeneration band keratopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "band keratopathy", "shortest_name_length": 16}
{"curie": "MONDO:0024287", "names": ["ANOMALY VASCULAR", "Vascular anomaly", "VASCULAR ANOMALY", "Vascular anomalies", "vascular malformation", "Vascular Malformation", "Vascular malformation", "Vascular malformation, NOS", "VM - Vascular malformation", "Congenital Vascular Anomaly", "Congenital vascular anomaly", "Congenital vascular disorder", "CONGENITAL VASCULAR ANOMALIES", "Vascular anomalies, congenital", "Congenital vascular abnormality", "Congenital vascular anomaly, NOS", "Congenital vascular disease, NOS", "congenital vascular malformation", "Congenital vascular malformation", "Congenital Vascular Malformations", "congenital malformations vascular", "Vascular malformation, congenital", "Congenital vascular disorder (disorder)", "Congenital vascular disease or syndrome", "Congenital vascular disorder (diagnosis)", "Congenital vascular malformation (disorder)", "congenital anomaly of cardiovascular system vascular disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital vascular malformation", "shortest_name_length": 16}
{"curie": "MONDO:0004371", "names": ["Spinal Multifocal Clear Cell Meningioma", "spinal multifocal clear cell meningioma", "multifocal clear cell meningioma of spine", "Multifocal Clear Cell Meningioma of Spine", "Multifocal Clear cell meningioma of Spine", "Multifocal Clear Cell Meningioma of the Spine", "multifocal clear cell meningioma of the spine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal multifocal clear cell meningioma", "shortest_name_length": 39}
{"curie": "UMLS:C1710176", "names": ["Lung Squamous Cell Carcinoma, Small Cell Variant", "Squamous Cell Lung Carcinoma, Small Cell Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Squamous Cell Carcinoma, Small Cell Variant", "shortest_name_length": 48}
{"curie": "UMLS:C3495917", "names": ["Advanced breast cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced breast cancer", "shortest_name_length": 22}
{"curie": "MONDO:0054732", "names": ["SPGF28", "spermatogenic failure 28", "SPERMATOGENIC FAILURE 28"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 28", "shortest_name_length": 6}
{"curie": "UMLS:C2828150", "names": ["HPV positive oropharyngeal squamous cell carcinoma", "Oropharyngeal HPV-Positive Squamous Cell Carcinoma", "HPV-Positive Oropharyngeal Squamous Cell Carcinoma", "HPV-Associated Oropharyngeal Squamous Cell Carcinoma", "Oropharyngeal Human Papillomavirus Positive Squamous Cell Carcinoma", "Oropharyngeal Human Papillomavirus-Positive Squamous Cell Carcinoma", "Human Papillomavirus Positive Oropharyngeal Squamous Cell Carcinoma", "Human papilloma virus positive oropharyngeal squamous cell carcinoma", "Human Papilloma Virus Positive Oropharyngeal Squamous Cell Carcinoma", "Human Papilloma Virus Associated Oropharyngeal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HPV positive oropharyngeal squamous cell carcinoma", "shortest_name_length": 50}
{"curie": "UMLS:C4683590", "names": ["Lugano Classification Stage II Bulky Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage II Bulky Hodgkin Lymphoma AJCC v8", "shortest_name_length": 61}
{"curie": "MONDO:0013314", "names": ["RP56", "RETINITIS PIGMENTOSA 56", "retinitis pigmentosa 56", "maculopathy, Impg2-related", "IMPG2 retinitis pigmentosa", "retinitis pigmentosa type 56", "retinitis pigmentosa caused by mutation in IMPG2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 56", "shortest_name_length": 4}
{"curie": "UMLS:C0855202", "names": ["Stage I Subdiaphragmatic Nodular Sclerosis Hodgkin Lymphoma", "Stage I Subdiaphragmatic Nodular Sclerosis Hodgkin's Disease", "Hodgkin's disease nodular sclerosis stage I subdiaphragmatic", "Stage I Subdiaphragmatic Nodular Sclerosis Hodgkin's Lymphoma", "Stage I Nodular Sclerosis Hodgkin's Disease below the Diaphragm", "Stage I Nodular Sclerosis Hodgkin's Lymphoma below the Diaphragm", "Stage I Subdiaphragmatic Nodular Sclerosis Classical Hodgkin Lymphoma", "Ann Arbor Stage I Subdiaphragmatic Nodular Sclerosis Classic Hodgkin Lymphoma", "Ann Arbor Stage I Subdiaphragmatic Nodular Sclerosis Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's disease nodular sclerosis stage I subdiaphragmatic", "shortest_name_length": 59}
{"curie": "MONDO:0100219", "names": ["GHISID2", "growth hormone insensitivity syndrome with immune dysregulation 2", "growth hormone insensitivity with immune dysregulation 2, autosomal dominant", "GROWTH HORMONE INSENSITIVITY SYNDROME WITH IMMUNE DYSREGULATION 2, AUTOSOMAL DOMINANT", "growth hormone insensitivity syndrome with immune dysregulation 2, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "growth hormone insensitivity syndrome with immune dysregulation 2, autosomal dominant", "shortest_name_length": 7}
{"curie": "UMLS:C4329260", "names": ["Acquired Hypoparathyroidism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired Hypoparathyroidism", "shortest_name_length": 27}
{"curie": "MONDO:0030064", "names": ["EA9", "EPISODIC ATAXIA, TYPE 9", "episodic ataxia, type 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "episodic ataxia, type 9", "shortest_name_length": 3}
{"curie": "MONDO:0008527", "names": ["Tarsal bar", "tarsal bar", "TARSAL FUSION", "tarsal fusion", "Tarsal fusion", "fusion; tarsal", "tarsal; fusion", "Tarsal fusions", "Tarsal coalition", "Tarsal Coalition", "tarsal coalition", "TARSAL COALITION", "Tarsal synostosis", "Tarsal Synostosis", "Tarsal synostoses", "Tarsal coalitions", "Tarsal Synostoses", "tarsal coalitions", "Fused ankle bones", "Tarsal Coalitions", "Synostoses, Tarsal", "Tarsal bone fusion", "Synostosis, Tarsal", "Tarsal bone fusions", "Tarsal bone synostosis", "Synostosis of tarsal bones", "tarsal coalition (diagnosis)", "Tarsal coalitions (disorder)", "Synostosis involving tarsal bones"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tarsal coalition", "shortest_name_length": 10}
{"curie": "UMLS:C1336282", "names": ["Stage II Bone Sarcoma", "Stage II Sarcoma of Bone", "Stage II Sarcoma of the Bone", "Stage II Bone Sarcoma AJCC v7", "Stage II Bone Sarcoma  AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Bone Sarcoma AJCC v7", "shortest_name_length": 21}
{"curie": "MONDO:0005724", "names": ["torula", "Torula", "Torulosis", "torulosis", "TORULOSIS", "Toruloses", "CRYPTOCOCCUS", "Cryptococcoses", "cryptococcoses", "Cryptococcosis", "CRYPTOCOCCOSIS", "cryptococcosis", "Cryptococcosis, NOS", "Busse-Buschke disease", "Cryptococcus Infection", "European blastomycosis", "cryptococcal infection", "C.neoformans infection", "European Blastomycosis", "Cryptococcal infection", "C neoformans Infection", "Infection, Cryptococcus", "Cryptococcus Infections", "Busse-Buschke's disease", "cryptococcus neoformans", "C neoformans Infections", "Cryptococcus neoformans", "Infection, C neoformans", "C. neoformans Infection", "European cryptococcosis", "Busse-Buschke (etiology)", "Infection, C. neoformans", "C. neoformans Infections", "Infections, C. neoformans", "Cryptococcosis (disorder)", "cryptococcosis (diagnosis)", "Cryptococcosis, unspecified", "Torula histolytica; infection", "Infection due to Cryptococcus", "Busse-Buschke (manifestation)", "infection; Torula histolytica", "Cryptococcus neoformans infection", "cryptococcus infection neoformans", "cryptococcus neoformans infection", "Cryptococcus neoformans Infection", "Infection, Cryptococcus neoformans", "infection; Cryptococcus neoformans", "Cryptococcus neoformans; infection", "Cryptococcus neoformans Infections", "Infection by Cryptococcus neoformans", "Cryptococcus neoformans infectious disease", "Cryptococcus neoformans disease or disorder", "infection; Blastomyces, blastomycotic, European", "Cryptococcus neoformans caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cryptococcosis", "shortest_name_length": 6}
{"curie": "MONDO:0012005", "names": ["growth failure, microcephaly, mental retardation, cataracts, large joint contractures, osteoporosis, cortical dysplasia, and cerebellar atrophy", "GROWTH FAILURE, MICROCEPHALY, MENTAL RETARDATION, CATARACTS, LARGE JOINT CONTRACTURES, OSTEOPOROSIS, CORTICAL DYSPLASIA, AND CEREBELLAR ATROPHY", "Growth Failure, Microcephaly, Mental Retardation, Cataracts, Large Joint Contractures, Osteoporosis, Cortical Dysplasia, and Cerebellar Atrophy", "growth failure, microcephaly, intellectual disability, cataracts, large joint contractures, osteoporosis, cortical dysplasia, and cerebellar atrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "growth failure, microcephaly, intellectual disability, cataracts, large joint contractures, osteoporosis, cortical dysplasia, and cerebellar atrophy", "shortest_name_length": 143}
{"curie": "UMLS:C1406988", "names": ["Vital Exhaustion", "exhaustion; vital", "vital; exhaustion", "vital exhaustion; state", "state; vital exhaustion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vital Exhaustion", "shortest_name_length": 16}
{"curie": "MONDO:0010544", "names": ["CCT", "CXN", "CTRCT40", "cataract 40", "CATARACT 40", "cataract type 40", "cataract 40 X-linked", "cataract 40, X-linked", "Cataract, total congenital", "Cataract, Congenital Total", "Cataract congenital X-linked", "cataract congenital X-linked", "cataract, congenital, X-linked", "CATARACT, CONGENITAL, X-LINKED", "NHS early-onset non-syndromic cataract", "CATARACT 40 WITH OR WITHOUT MICROCORNEA", "cataract 40 with or without microcornea", "early-onset non-syndromic cataract caused by mutation in NHS", "Cataract, congenital, with microcornea or slight microphthalmia", "cataract, congenital, with microcornea or slight microphthalmia", "Cataract, total congenital with posterior sutural opacities in Heterozygotes", "CATARACT, CONGENITAL TOTAL, WITH POSTERIOR SUTURAL OPACITIES IN HETEROZYGOTES", "Cataract, Congenital Total, With Posterior Sutural Opacities In Heterozygotes", "cataract, congenital total, with posterior sutural opacities in heterozygotes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 40", "shortest_name_length": 3}
{"curie": "UMLS:C0079745", "names": ["NHL", "Grade 3", "NH lymphoma", "FL lymphoma", "Grade 3 Follicular Lymphoma", "follicular lymphoma grade 3", "grade 3 follicular lymphoma", "follicular grade 3 lymphoma", "Follicular Lymphoma Grade 3", "Lymphoma histiocytic nodular", "Nodular Histiocytic Lymphoma", "Follicular lymphoma, grade 3", "Follicular Lymphoma, Grade 3", "nodular histiocytic lymphoma", "histiocytic nodular lymphoma", "Grade III Follicular Lymphoma", "Lymphoma, Follicular, Grade 3", "grade III follicular lymphoma", "Lymphoma, Nodular Histiocytic", "Nodular Histiocytic Lymphomas", "Histiocytic Lymphoma, Nodular", "lymphoma, nodular histiocytic", "Large cell follicular lymphoma", "Lymphomas, Nodular Histiocytic", "large cell follicular lymphoma", "lymphoma; nodular, histiocytic", "Lymphoma, Histiocytic, Nodular", "nodular; lymphoma, histiocytic", "Follicular Large-Cell Lymphoma", "follicular large cell lymphoma", "Histiocytic Lymphomas, Nodular", "Follicular Large Cell Lymphoma", "lymphoma, follicular large cell", "Lymphoma, Follicular Large Cell", "Large-Cell Lymphoma, Follicular", "Follicular Large-Cell Lymphomas", "Lymphoma, Follicular Large-Cell", "Large Cell Lymphoma, Follicular", "Lymphoma, Large-Cell, Follicular", "Large-Cell Lymphomas, Follicular", "Lymphoma, Large Cell, Follicular", "Large Lymphoid Lymphoma, Nodular", "Lymphomas, Follicular Large-Cell", "Lymphoma, Large Lymphoid, Nodular", "Germinoblastic sarcoma, follicular", "Malignant lymphoma histiocytic nodular", "grade 3 follicular lymphoma (diagnosis)", "Malignant lymphoma, histiocytic, nodular", "grade III follicular large cell lymphoma", "Grade III Follicular Large Cell Lymphoma", "Malignant lymphoma - histiocytic, nodular", "follicular malignant lymphoma, large cell", "Malignant lymphoma, large cell, follicular", "Malignant lymphoma, noncleaved, follicular", "Follicular malignant lymphoma - large cell", "WHO Follicular Lymphoma Histologic Grade 3", "follicular, centroblastic malignant lymphoma", "Malignant lymphoma - non-cleaved, follicular", "malignant follicular lymphoma, centroblastic", "Malignant Lymphoma Centroblastic, Follicular", "Nodular Large Follicular Center-Cell Lymphoma", "Malignant lymphoma, centroblastic, follicular", "Nodular Large Follicular Center Cell Lymphoma", "Follicular Lymphoma, Predominantly Large Cell", "Malignant lymphoma, large cell, follicular NOS", "Malignant lymphoma, noncleaved, follicular, NOS", "Lymphoma, Nodular, Large Follicular Center Cell", "Lymphoma, Nodular, Large Follicular Center-Cell", "Malignant lymphoma, large cell, follicular, NOS", "Malignant lymphoma, centroblastic type, follicular", "Malignant lymphoma, large cleaved cell, follicular", "follicular malignant lymphoma, large cell (diagnosis)", "[M]Malignant lymphoma, centroblastic type, follicular", "Malignant lymphoma, large cell, noncleaved, follicular", "Follicular lymphoma, grade 3 (morphologic abnormality)", "malignant neoplasm nodular lymphoma follicular grade 3", "malignant follicular lymphoma, centroblastic (diagnosis)", "Malignant lymphoma, follicular, predominately large cell", "Malignant lymphoma, centroblastic type, follicular (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoma, Large-Cell, Follicular", "shortest_name_length": 3}
{"curie": "UMLS:C4324474", "names": ["Cytomegalovirus nephritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cytomegalovirus nephritis", "shortest_name_length": 25}
{"curie": "MONDO:0007761", "names": ["IV; Frederickson", "Frederickson; IV", "Type IV lipidemia", "Type IV lipidaemia", "hyperlipidemia type iv", "prebetalipoproteinemia", "pure hyperglyceridemia", "Pure hyperglyceridemia", "Type IV hyperlipidemia", "HYPERLIPIDEMIA TYPE IV", "type iv hyperlipidemia", "Pure hyperglyceridaemia", "Type IV hyperlipidaemia", "Hyperlipidemia, group B", "Hyperlipidemia, Group B", "Endogenous hyperlipemia", "hyperlipidemia; group B", "Endogenous hyperlipaemia", "Endogenous hyperlipidemia", "VLDL hyperlipoproteinemia", "hyperlipidemia endogenous", "endogenous hyperlipidemia", "Endogenous hyperlipidaemia", "endogenous hyperlipidaemia", "Hyperprebetalipoproteinemia", "hyperprebetalipoproteinemia", "HYPERPREBETALIPOPROTEINEMIA", "hyperlipoproteinemia type 4", "Type IV hyperlipoproteinemia", "endogenous hyperglyceridemia", "hyperlipoproteinemia, type 4", "Type IV Hyperlipoproteinemia", "Endogenous hyperglyceridemia", "type iv hyperlipoproteinemia", "Hyperlipoproteinemia Type IV", "HYPERLIPOPROTEINEMIA TYPE IV", "hyperlipoproteinemia type IV", "Fredrickson Type IV lipidemia", "Hyper prebeta lipoproteinemia", "hyperlipoproteinemia, type IV", "Type IV Hyperlipoproteinemias", "Familial hypertriglyceridemia", "Fredrickson Type IV Lipidemia", "familial hypertriglyceridemia", "Hyperlipoproteinemia, Type IV", "Fredrickson type IV lipidemia", "HYPERLIPOPROTEINEMIA, TYPE IV", "Fredrickson type IV Lipidemia", "Type IV, Hyperlipoproteinemia", "Familial Hypertriglyceridemia", "Type IV hyperlipoproteinaemia", "Familial hypertriglyceridaemia", "Hyperlipoproteinemias, Type IV", "Fredrickson Type IV lipidaemia", "essential hypertriglyceridemia", "Hypertriglyceridemia, Familial", "Fredrickson type IV lipidaemia", "familial hypertriglyceridaemia", "hypertriglyceridemia; essential", "Hypertriglyceridemia, essential", "Pure hyperglyceridemia (disorder)", "very-low-density-lipoprotein-type", "Fredrickson type IV hyperlipidemia", "pure hyperglyceridemia (diagnosis)", "carbohydrate inducible hyperlipemia", "carbohydrate-inducible hyperlipemia", "CARBOHYDRATE-INDUCIBLE HYPERLIPEMIA", "Carbohydrate Inducible Hyperlipemia", "Carbohydrate-Inducible Hyperlipemia", "Carbohydrate Inducible Hyperlipemias", "familial hyperprebetalipoproteinemia", "Familial Hyperlipoproteinemia Type 4", "Carbohydrate-Inducible Hyperlipemias", "Endogenous hyperlipidemia (disorder)", "Inducible Hyperlipemia, Carbohydrate", "Hyperlipemia, Carbohydrate-Inducible", "Hyperlipemia, Carbohydrate Inducible", "Familial Type IV Hyperlipoproteinemia", "familial type IV hyperlipoproteinemia", "VLDL hyperlipoproteinemia (diagnosis)", "endogenous hyperlipidemia (diagnosis)", "Hyperlipemias, Carbohydrate-Inducible", "familial hyperlipoproteinemia type IV", "Inducible Hyperlipemias, Carbohydrate", "Hyperlipemias, Carbohydrate Inducible", "Fredrickson Type IV hyperlipoproteinemia", "hyperlipoproteinemia type IV (diagnosis)", "Fredrickson type IV hyperlipoproteinemia", "Familial hypertriglyceridemia (disorder)", "Fredrickson; type IV hyperlipoproteinemia", "hyperlipoproteinemia; Fredrickson type IV", "familial hypertriglyceridemia (diagnosis)", "Carbohydrate induced hyperlipoproteinemia", "Fredrickson type IV hyperlipoproteinaemia", "essential hypertriglyceridemia (diagnosis)", "Hyperlipoproteinemia, Frederickson type IV", "Fredrickson's hyperlipoproteinemia, type IV", "Fredrickson type IV hyperlipidemia (diagnosis)", "Very-low-density-lipoid-type hyperlipoproteinemia", "Fredrickson type IV hyperlipoproteinemia (disorder)", "very-low-density-lipoprotein-type; hyperlipoproteinemia", "hyperlipoproteinemia; very-low-density-lipoprotein-type", "Very-low-density-lipoprotein-type [VLDL] hyperlipoproteinemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperlipoproteinemia type IV", "shortest_name_length": 16}
{"curie": "UMLS:C4721926", "names": ["stage IIIA uterine sarcoma", "Stage IIIA Uterine Sarcoma", "Stage IIIA Uterine Sarcoma AJCC v7", "stage IIIA uterine sarcoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Uterine Sarcoma AJCC v7", "shortest_name_length": 26}
{"curie": "UMLS:C2981389", "names": ["Stage IIIB Appendix Cancer", "Stage IIIB Appendix Carcinoma", "Stage IIIB Appendix Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Appendix Carcinoma AJCC v7", "shortest_name_length": 26}
{"curie": "MONDO:0004952", "names": ["hd", "HD", "HL", "CHL", "Hodgkin", "HODGINS", "hodgkin disease", "HODGKIN DISEASE", "Hodgkin Disease", "Hodgkin disease", "Hodgkin sarcoma", "Disease, Hodgkin", "sarcoma; Hodgkin", "HODGKINS DISEASE", "Hodgkin Lymphoma", "Hodgkins Disease", "Sarcoma;Hodgkins", "LYMPHOMA HODGKIN", "disease; Hodgkin", "Hodgkins sarcoma", "Hodgkin; sarcoma", "hodgkins disease", "Hodgkin lymphoma", "hodgkin lymphoma", "Disease;Hodgkins", "Hodgkins disease", "HODGKIN LYMPHOMA", "Hodgkin`s disease", "hodgkins lymphoma", "Hodgkin granuloma", "Disease, Hodgkins", "hodgkin lymphomas", "lymphoma; Hodgkin", "Lymphoma;Hodgkins", "Hodgkin's disease", "Hodgkin's Disease", "Hodgkin's Sarcoma", "Hodgkin Granuloma", "Hodgkin's sarcoma", "hodgkin's disease", "Hodgkins Lymphoma", "hodgkins diseases", "HODGKIN'S DISEASE", "Hodgkins lymphoma", "Hodgkin; lymphoma", "Lymphoma, Hodgkin", "Hodgkin's Lymphoma", "Hodgkin's lymphoma", "hodgkin's lymphoma", "Hodgkin; granuloma", "Hodgkins Granuloma", "Lymphoma, Hodgkins", "Granuloma, Hodgkin", "granuloma; Hodgkin", "hodgkins lymphomas", "Disease, Hodgkin's", "Granuloma, Hodgkins", "Hodgkin's Granuloma", "Hodgkin's granuloma", "Lymphoma, Hodgkin's", "hodgkin's lymphomas", "lymphoma, Hodgkin's", "Malignant Granuloma", "Hodgkin disease, NOS", "Malignant Granulomas", "Lymphogranulomatosis", "hodgkin disease (HD)", "lymphogranulomatosis", "Granuloma, Hodgkin's", "[M]Hodgkin's disease", "malignant; granuloma", "Granuloma, Malignant", "granuloma; malignant", "Hodgkin's disease NOS", "Hodgkin Lymphoma, NOS", "Hodgkin lymphoma, NOS", "Hodgkins Paragranuloma", "Hodgkin's lymphoma NOS", "Hodgkin; paragranuloma", "Hodgkin's disease, NOS", "HD - Hodgkin's disease", "paragranuloma; Hodgkin", "Hodgkin's paragranuloma", "Hodgkin's Paragranuloma", "Hodgkin lymphoma sarcoma", "HODGKINS DISEASE SYSTEMIC", "Malignant Lymphogranuloma", "Malignant lymphogranuloma", "LYMPHOMA, HODGKIN, CLASSIC", "Lymphogranuloma, malignant", "Hodgkin's disease/lymphoma", "Hodgkin paragranuloma, NOS", "Malignant Lymphogranulomas", "Hodgkin lymphoma granuloma", "Lymphogranuloma, Malignant", "hodgkin's lymphoma disease", "Lymphomas Hodgkin's disease", "Lymphogranulomas, Malignant", "Hodgkin's paragranuloma NOS", "Malignant lymphoma, Hodgkin", "Hodgkin's disease (clinical)", "Hodgkin's disease (disorder)", "Hodgkin's sarcoma (clinical)", "Hodgkin's sarcoma (disorder)", "Malignant Hodgkin's lymphoma", "Hodgkin's paragranuloma, NOS", "Hodgkin lymphoma (diagnosis)", "Hodgkin lymphoma, unspecified", "Malignant lymphoma, Hodgkin's", "Hodgkin's disease, unspecified", "Hodgkin's granuloma (clinical)", "Hodgkin's granuloma (disorder)", "Malignant lymphogranulomatosis", "Hodgkin lymphoma paragranuloma", "Lymphogranulomatosis, malignant", "lymphogranulomatosis (malignant)", "Hodgkin's paragranuloma, nodular", "Hodgkin's paragranuloma (clinical)", "Malignant lymphoma, Hodgkin's type", "Hodgkin's disease, unspecified type", "Hodgkin lymphoma sarcoma (diagnosis)", "Hodgkin lymphoma granuloma (diagnosis)", "stage I Subdiaphragmatic Hodgkin Lymphoma", "Hodgkin sarcoma (morphologic abnormality)", "stage I subdiaphragmatic Hodgkin lymphoma", "Hodgkin lymphoma (morphologic abnormality)", "Hodgkin lymphoma paragranuloma (diagnosis)", "stage II subdiaphragmatic Hodgkin lymphoma", "stage II Subdiaphragmatic Hodgkin Lymphoma", "Hodgkin granuloma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkins lymphoma", "shortest_name_length": 2}
{"curie": "MONDO:0032831", "names": ["PCH13", "pontocerebellar hypoplasia type 13", "Pontocerebellar hypoplasia type 13", "PONTOCEREBELLAR HYPOPLASIA, TYPE 13", "pontocerebellar hypoplasia, type 13"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pontocerebellar hypoplasia, type 13", "shortest_name_length": 5}
{"curie": "UMLS:C2986664", "names": ["Multicentric Breast Cancer", "multicentric breast cancer", "Multicentric Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Multicentric Breast Carcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0015593", "names": ["limbic encephalitis with nCMAgs antibodies", "limbic encephalitis with novel cell membrane antigen antibodies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "limbic encephalitis with nCMAgs antibodies", "shortest_name_length": 42}
{"curie": "UMLS:C5555720", "names": ["Ovarian Neuroectodermal-Type Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Neuroectodermal-Type Tumor", "shortest_name_length": 34}
{"curie": "MONDO:0022822", "names": ["congenital cardiovascular shunt"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital cardiovascular shunt", "shortest_name_length": 31}
{"curie": "OMIM:120050", "names": ["CB3S", "CXB3S", "COXSACKIEVIRUS B3 SUSCEPTIBILITY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 4}
{"curie": "MONDO:0020512", "names": ["T-ALL", "precursor T-cell acute lymphocytic leukemia", "precursor T-cell acute lymphoblastic leukemia", "precursor T-cell lymphoblastic leukemia-lymphoma", "precursor T-cell acute lymphocytic leukemia/lymphoma", "precursor T-cell acute lymphoblastic leukemia/lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "precursor T-cell acute lymphoblastic leukemia", "shortest_name_length": 5}
{"curie": "UMLS:C3897223", "names": ["Untreated Pilomyxoid Astrocytoma", "untreated childhood pilomyxoid astrocytoma", "Untreated Childhood Pilomyxoid Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Untreated Childhood Pilomyxoid Astrocytoma", "shortest_name_length": 32}
{"curie": "MONDO:0012494", "names": ["testicle microlithiasis", "Testicular Microlithiasis", "Testicular microlithiasis", "TESTICULAR MICROLITHIASIS", "testicular microlithiasis", "microlithiasis of testicle", "testicular microlithiasis (disease)", "Testicular microlithiasis (disorder)", "microlithiasis of testicle (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular microlithiasis", "shortest_name_length": 23}
{"curie": "MONDO:0023134", "names": ["FUMHD", "variant of Mucha-Habermann disease", "ulceronecrotic Mucha-Habermann disease", "Ulceronecrotic Mucha-Habermann disease", "Febrile ulceronecrotic Mucha-Habermann disease", "febrile ulceronecrotic Mucha-Habermann disease", "Febrile Ulceronecrotic Mucha-Habermann disease", "Febrile ulceronecrotic pityriasis lichenoides acuta", "febrile ulceronecrotic pityriasis lichenoides acuta", "Febrile ulceronecrotic pityriasis lichenoides acuta (disorder)", "A severe variant of pityriasis lichenoides et varioliformis acuta (PLEVA)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "febrile ulceronecrotic Mucha-Habermann disease", "shortest_name_length": 5}
{"curie": "MONDO:0016692", "names": ["PMA", "pilomyxoid astrocytoma", "Pilomyxoid Astrocytoma", "Pilomyxoid astrocytoma", "Pilomyxoid astrocytoma (disorder)", "Pilomyxoid astrocytoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pilomyxoid astrocytoma", "shortest_name_length": 3}
{"curie": "UMLS:C4049702", "names": ["FSGS", "FSGS (NOS)", "Focal Segmental Glomerulosclerosis (NOS)", "Focal Segmental Glomerulosclerosis, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Focal Segmental Glomerulosclerosis, Not Otherwise Specified", "shortest_name_length": 4}
{"curie": "UMLS:C0274312", "names": ["Graft complication", "Graft complications", "Complication of graft", "complications of graft", "Graft complications (disorder)", "complications of graft (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Graft complications", "shortest_name_length": 18}
{"curie": "MONDO:0100121", "names": ["SCN4A-related myopathy, autosomal recessive", "myopathy with ptosis and mild dystrophic pattern", "congenital myopathy with severe fetal hypokinesia", "congenital myopathy with \"corona\" fibers, selective muscle atrophy, and craniosynostosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SCN4A-related myopathy, autosomal recessive", "shortest_name_length": 43}
{"curie": "UMLS:C3899662", "names": ["Fibrillary Astrocytoma", "Childhood Fibrillary Astrocytoma", "childhood fibrillary astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Fibrillary Astrocytoma", "shortest_name_length": 22}
{"curie": "MONDO:0002647", "names": ["LARYNGITIS", "laryngitis", "Laryngitis", "Laryngitides", "Laryngitis NOS", "Larynx inflamed", "Laryngitis, NOS", "larynx inflammation", "Laryngitis (disorder)", "Laryngeal Inflammation", "laryngeal inflammation", "laryngeal Inflammation", "inflammation of larynx", "laryngitis (diagnosis)", "Laryngeal inflammation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laryngitis", "shortest_name_length": 10}
{"curie": "MONDO:0018502", "names": ["hereditary gastric cancer", "hereditary cancer of stomach"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary gastric cancer", "shortest_name_length": 25}
{"curie": "MONDO:0100066", "names": ["TH-deficient progressive infantile encephalopathy", "tyrosine hydroxylase-deficient progressive infantile encephalopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "TH-deficient progressive infantile encephalopathy", "shortest_name_length": 49}
{"curie": "MONDO:0021650", "names": ["body of uterus NET", "Uterine Corpus Neuroendocrine Tumor", "body of uterus neuroendocrine tumor", "uterine corpus neuroendocrine tumor", "uterine corpus neuroendocrine neoplasm", "body of uterus neuroendocrine neoplasm", "Uterine Corpus Neuroendocrine Neoplasm", "neuroendocrine neoplasm of body of uterus", "body of uterus neuroendocrine tumor, well differentiated, low or intermediate grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine corpus neuroendocrine neoplasm", "shortest_name_length": 18}
{"curie": "UMLS:C0851979", "names": ["Esophageal infection", "esophageal infection", "Esophageal Infection", "Esophagitis infection", "esophageal infections", "Esophageal infections", "Oesophageal infection", "Oesophagitis infection", "Oesophageal infections", "esophageal infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Infection", "shortest_name_length": 20}
{"curie": "MONDO:0013117", "names": ["Peoa5", "PEOA5", "autosomal dominant progressive external ophthalmoplegia 5", "PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL DOMINANT 5", "progressive external ophthalmoplegia, autosomal dominant 5", "Progressive External Ophthalmoplegia, Autosomal Dominant, 5", "RRM2B progressive external ophthalmoplegia with mitochondrial DNA deletions", "autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 5", "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5", "PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 5", "Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5", "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant type 5", "progressive external ophthalmoplegia with mitochondrial DNA deletions caused by mutation in RRM2B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5", "shortest_name_length": 5}
{"curie": "UMLS:C4724168", "names": ["Recurrent Aggressive Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Aggressive Non-Hodgkin Lymphoma", "shortest_name_length": 41}
{"curie": "UMLS:C5243761", "names": ["Polyomavirus viremia", "Polyomavirus viraemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Polyomavirus viremia", "shortest_name_length": 20}
{"curie": "MONDO:0001929", "names": ["ASCENDING CHOLANGITIS", "CHOLANGITIS ASCENDING", "ascending cholangitis", "Ascending Cholangitis", "Ascending cholangitis", "CHOLANGITIS, ASCENDING", "Ascending cholangitis (disorder)", "ascending cholangitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ascending cholangitis", "shortest_name_length": 21}
{"curie": "UMLS:C1257799", "names": ["Choledochal Cyst, Type V", "Intrahepatic Choledochal Cyst", "Choledochal Cyst, Intrahepatic", "Cyst, Intrahepatic Choledochal", "Intrahepatic Choledochal Cysts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Choledochal Cyst, Type V", "shortest_name_length": 24}
{"curie": "UMLS:C3839062", "names": ["Malignant PEComa", "PEComa, malignant", "Malignant PEComa, NOS", "Perivascular epithelioid tumor, malignant", "Malignant PEComa, Not Otherwise Specified", "Perivascular epithelioid tumour, malignant", "Perivascular epithelioid cell tumor, malignant", "Perivascular epithelioid tumor, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perivascular epithelioid tumor, malignant", "shortest_name_length": 16}
{"curie": "MONDO:0003470", "names": ["Cellular Ependymoma", "cellular ependymoma", "Cellular ependymoma", "Clear cell ependymoma", "Clear Cell Ependymoma", "Cellular ependymoma (morphologic abnormality)", "Clear cell ependymoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cellular ependymoma", "shortest_name_length": 19}
{"curie": "UMLS:C4744489", "names": ["Refractory Neurofibromatosis Type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Neurofibromatosis Type 1", "shortest_name_length": 35}
{"curie": "UMLS:C2984898", "names": ["Intraocular Schwannoma", "Benign Intraocular Schwannoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraocular Schwannoma", "shortest_name_length": 22}
{"curie": "UMLS:C0920166", "names": ["Catheter site bleeding", "Catheter site hemorrhage", "Catheter site haemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Catheter site bleeding", "shortest_name_length": 22}
{"curie": "UMLS:C0339881", "names": ["injury; larynx", "larynx; injury", "injury of larynx", "laryngeal injury", "laryngeal trauma", "Injury of larynx", "Laryngeal Injury", "Laryngeal trauma", "Laryngeal Trauma", "Laryngeal injury", "Injury of larynx (disorder)", "injury of larynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of larynx", "shortest_name_length": 14}
{"curie": "MONDO:0008203", "names": ["PASSOVOY FACTOR DEFECT", "Passovoy factor defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Passovoy factor defect", "shortest_name_length": 22}
{"curie": "UMLS:C0574019", "names": ["duodenal web", "Duodenal Web", "Duodenal web", "Duodenal diaphragm", "Duodenal web (disorder)", "duodenal web (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Duodenal web", "shortest_name_length": 12}
{"curie": "UMLS:C0151450", "names": ["Secondary Sjogren Syndrome", "Secondary Sjögren syndrome", "Secondary Sjögren Syndrome", "Secondary Sjogren's syndrome", "Secondary Sjögren's syndrome", "Sjogren's Syndrome, Secondary", "Sjogren's syndrome, secondary", "Secondary Sjögren's syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary Sjögren's syndrome", "shortest_name_length": 26}
{"curie": "UMLS:C5575231", "names": ["BFIS", "BFIE", "Benign Familial Infantile Seizures", "Benign Familial Infantile Epilepsy", "Benign Familial Infantile Convulsions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Familial Infantile Seizures", "shortest_name_length": 4}
{"curie": "UMLS:C4526968", "names": ["Stage II Gastric and Omental GIST AJCC v8", "Stage II Gastric and Omental Gastrointestinal Stromal Tumor AJCC v8", "Stage II Gastric (Stomach) and Omental Gastrointestinal Stromal Tumor (GIST)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Gastric and Omental Gastrointestinal Stromal Tumor AJCC v8", "shortest_name_length": 41}
{"curie": "MONDO:0030312", "names": ["SCAR29", "NEDHCA", "BAVAHAKA", "Barakat-Van Ham-Kaya syndrome", "BARAKAT-VAN HAM-KAYA SYNDROME", "autosomal recessive spinocerebellar ataxia 29", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 29", "spinocerebellar ataxia, autosomal recessive 29", "NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND CEREBELLAR ATAXIA", "neurodevelopmental disorder with hypotonia and cerebellar ataxia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia, autosomal recessive 29", "shortest_name_length": 6}
{"curie": "UMLS:C0280358", "names": ["Stage IV Lip and Oral Cavity Squamous Cell Cancer", "Stage IV Lip and Oral Cavity Squamous Cell Carcinoma", "lip and oral cavity squamous cell carcinoma, stage IV", "oral cavity and lip squamous cell carcinoma, stage IV", "lip and oral cavity squamous cell carcinoma, metastatic", "oral cavity and lip squamous cell carcinoma, metastatic", "epidermoid carcinoma of the lip and oral cavity, stage IV", "epidermoid carcinoma of the lip and oral cavity, metastatic", "stage IV squamous cell carcinoma of the lip and oral cavity", "squamous cell carcinoma of the lip and oral cavity, stage IV", "Stage IV Lip and Oral Cavity Squamous Cell Carcinoma AJCC v7", "Stage IV Lip and Oral Cavity Squamous Cell Carcinoma AJCC v6", "metastatic squamous cell carcinoma of the lip and oral cavity", "squamous cell carcinoma of the lip and oral cavity, metastatic", "Stage IV Lip and Oral Cavity Squamous Cell Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Lip and Oral Cavity Squamous Cell Carcinoma AJCC v6 and v7", "shortest_name_length": 49}
{"curie": "UMLS:C1571983", "names": ["Late paraphrenia", "Paraphrenia (late)", "Involutional paraphrenia", "Involutional Paraphrenia", "paraphrenia involutional", "Paraphrenia, Involutional", "Involutional Paraphrenias", "Paraphrenias, Involutional", "Involutional paraphrenia (disorder)", "Involutional paraphrenia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Involutional paraphrenia", "shortest_name_length": 16}
{"curie": "UMLS:C1736136", "names": ["Metapneumovirus infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metapneumovirus infection", "shortest_name_length": 25}
{"curie": "UMLS:C0948281", "names": ["malignant syndrome", "malignant syndrome nos", "Malignant syndrome NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant syndrome NOS", "shortest_name_length": 18}
{"curie": "UMLS:C4288142", "names": ["TERC Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "TERC Deficiency", "shortest_name_length": 15}
{"curie": "UMLS:C1336223", "names": ["Stage IIIB Liver Cancer", "Stage IIIB Liver Carcinoma", "Stage IIIB Liver Cell Carcinoma", "Stage IIIB Hepatocellular Cancer", "Stage IIIB Carcinoma of Liver Cells", "Stage IIIB Hepatocellular Carcinoma", "Stage IIIB Carcinoma of the Liver Cells", "Stage IIIB Hepatocellular Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Hepatocellular Carcinoma AJCC v7", "shortest_name_length": 23}
{"curie": "UMLS:C1336160", "names": ["Stage IIA Esophageal Squamous Cell Cancer", "Stage IIA Esophagus Squamous Cell Carcinoma", "Stage IIA Esophageal Squamous Cell Carcinoma", "Stage IIA Squamous Cell Carcinoma of Esophagus", "Stage IIA Squamous Cell Carcinoma of the Esophagus", "Stage IIA Esophageal Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Esophageal Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 41}
{"curie": "UMLS:C3164625", "names": ["Pelvic Sarcoma", "Sarcoma of pelvis", "Sarcoma of Pelvis", "Sarcoma of the Pelvis", "Sarcoma of pelvis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sarcoma of pelvis", "shortest_name_length": 14}
{"curie": "MONDO:0020438", "names": ["atrial septal aneurysm", "Atrial septal aneurysm", "Atrial septal dilatation", "aneurysm of atrial septal wall", "Atrial septal aneurysm (disorder)", "aneurysm of atrial septal wall (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial septal aneurysm", "shortest_name_length": 22}
{"curie": "UMLS:C3274558", "names": ["Great Vessel Abnormality", "Great Vessels Abnormality", "Great vessel abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Great vessel abnormalities", "shortest_name_length": 24}
{"curie": "MONDO:0011577", "names": ["MYPOP", "IBM3, FORMERLY", "congenital myopathy 6", "inclusion body myopathy 3", "proximal myopathy and ophthalmoplegia", "myopathy, proximal, and ophthalmoplegia", "MYOPATHY, proximal, and ophthalmoplegia", "MYOPATHY, PROXIMAL, WITH OPHTHALMOPLEGIA", "inclusion body myopathy 3, autosomal dominant", "Inclusion Body Myopathy 3, Autosomal Dominant", "INCLUSION BODY MYOPATHY 3, AUTOSOMAL DOMINANT", "INCLUSION BODY MYOPATHY 3, AUTOSOMAL DOMINANT, FORMERLY", "inclusion body myopathy 3, autosomal dominant, formerly", "myopathy with congenital joint contractures, ophthalmoplegia, and rimmed vacuoles", "Myopathy with Congenital Joint Contractures, Ophthalmoplegia, and Rimmed Vacuoles", "MYOPATHY WITH CONGENITAL JOINT CONTRACTURES, OPHTHALMOPLEGIA, AND RIMMED VACUOLES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy, proximal, and ophthalmoplegia", "shortest_name_length": 5}
{"curie": "MONDO:0005481", "names": ["nickel sensitivity", "Nickel sensitivity", "nickel sensitivities", "Contact dermatitis due to nickel", "contact dermatitis due to nickel", "Contact dermatitis caused by nickel", "contact dermatitis due to nickel (diagnosis)", "Contact dermatitis caused by nickel (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "contact dermatitis due to nickel", "shortest_name_length": 18}
{"curie": "MONDO:0041086", "names": ["Anxious depression", "Anxiety depression", "anxiety depression", "depression anxiety", "depression; anxiety", "anxiety; depression", "depression with anxiety", "Depression with anxiety", "anxiety with depression", "Anxiety with depression", "anxiety depression mixed", "mixed anxiety depression", "Mixed anxiety & depressive", "depression with anxiety (diagnosis)", "Mixed anxiety and depressive disorder", "mixed anxiety and depressive disorder", "disorder; mixed, anxiety and depressive", "mixed; disorder, anxiety and depressive", "Mixed anxiety and depressive disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed anxiety and depressive disorder", "shortest_name_length": 18}
{"curie": "MONDO:0032835", "names": ["SEDN", "spondyloepiphyseal dysplasia Nishimura type", "spondyloepiphyseal dysplasia, nishimura type", "SPONDYLOEPIPHYSEAL DYSPLASIA, NISHIMURA TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepiphyseal dysplasia, nishimura type", "shortest_name_length": 4}
{"curie": "UMLS:C1335098", "names": ["occult NSCLC", "NSCLC, occult", "occult non-oat cell lung cancer", "occult nonsmall-cell lung cancer", "occult nonsmall cell lung cancer", "non-oat cell lung cancer, occult", "occult non-small cell lung cancer", "Occult Non-Small Cell Lung Cancer", "lung cancer, non-oat cell, occult", "nonsmall cell lung cancer, occult", "nonsmall-cell lung cancer, occult", "lung cancer, nonsmall cell, occult", "non-small cell lung cancer, occult", "Occult Lung Non-Small Cell Carcinoma", "Occult Non-Small Cell Lung Carcinoma", "Occult Non-Small Cell Carcinoma of Lung", "occult stage non-small cell lung cancer", "Occult Non-Small Cell Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Occult Lung Non-Small Cell Carcinoma", "shortest_name_length": 12}
{"curie": "UMLS:C5206602", "names": ["Paratesticular Mammary-Type Myofibroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paratesticular Mammary-Type Myofibroblastoma", "shortest_name_length": 44}
{"curie": "MONDO:0100327", "names": ["familial hypercholanemia", "hypercholanemia, familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypercholanemia, familial", "shortest_name_length": 24}
{"curie": "MONDO:0016453", "names": ["foodborne botulism", "Foodborne botulism", "Foodborne Botulism", "Botulism, Foodborne", "Foodborne Botulisms", "Intoxication botulism", "intoxication botulism", "Botulism food poisoning", "Foodborne botulism (disorder)", "botulism due to food poisoning", "foodborne botulism (diagnosis)", "Food poisoning due to Clostridium botulinum", "food; poisoning, due to Clostridium botulinum", "poisoning; food, due to Clostridium botulinum", "Food poisoning due to Clostridium botulinum toxin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "foodborne botulism", "shortest_name_length": 18}
{"curie": "UMLS:C0677955", "names": ["Stage I Non-Hodgkin Lymphoma", "Non-Hodgkin's lymphoma stage I", "Non-Hodgkin's Lymphoma Stage I", "Stage I Non-Hodgkin's Lymphoma", "Non-Hodgkin's lymphoma NOS stage I", "Ann Arbor Stage I Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Non-Hodgkin Lymphoma", "shortest_name_length": 28}
{"curie": "UMLS:C1332280", "names": ["Grade 3 Brainstem Glioma", "Grade 3 Brain Stem Glioma", "Grade III Brainstem Glioma", "Anaplastic Brainstem Glioma", "Brainstem Glioma, Grade III", "Grade III Brain Stem Glioma", "Grade 3 Glioma of Brainstem", "Anaplastic Brain Stem Glioma", "Brain Stem Glioma, Grade III", "Grade 3 Glioma of Brain Stem", "Grade III Glioma of Brainstem", "Grade III Glioma of Brain Stem", "Anaplastic Glioma of Brainstem", "Grade 3 Glioma of the Brainstem", "Anaplastic Glioma of Brain Stem", "Grade 3 Glioma of the Brain Stem", "Undifferentiated Brainstem Glioma", "Grade III Glioma of the Brainstem", "Anaplastic Glioma of the Brainstem", "Undifferentiated Brain Stem Glioma", "Grade III Glioma of the Brain Stem", "Anaplastic Glioma of the Brain Stem", "Undifferentiated Glioma of Brainstem", "Undifferentiated Glioma of Brain Stem", "Undifferentiated Glioma of the Brainstem", "Undifferentiated Glioma of the Brain Stem"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anaplastic Brain Stem Glioma", "shortest_name_length": 24}
{"curie": "MONDO:0006833", "names": ["Lingual goitre", "Lingual goiter", "lingual goiter", "Lingual Goiter", "Goiter, Lingual", "Lingual Goiters", "Goiters, Lingual", "Lingual goiter (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lingual goiter", "shortest_name_length": 14}
{"curie": "UMLS:C0434437", "names": ["sprain joint", "joint sprain", "Joint sprain", "joint sprains", "Sprain of joint", "SPRAINS OF OTHER JOINTS", "sprain of joint ligament", "Sprain of ligament of joint", "sprain of joint ligament (diagnosis)", "Sprain of ligament of joint (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joint sprain", "shortest_name_length": 12}
{"curie": "MONDO:0014093", "names": ["RP66", "retinitis pigmentosa 66", "RETINITIS PIGMENTOSA 66", "RBP3 retinitis pigmentosa", "retinitis pigmentosa type 66", "retinitis pigmentosa caused by mutation in RBP3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 66", "shortest_name_length": 4}
{"curie": "UMLS:C0151547", "names": ["CATARACT SPECIFIED", "Cataract specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cataract specified", "shortest_name_length": 18}
{"curie": "MONDO:0005240", "names": ["Nephropathy", "nephropathy", "NEPHROPATHY", "Renal Disease", "nephropathies", "Kidney damage", "renal disease", "Nephropathies", "RENAL DISEASE", "Renal disease", "damage; renal", "Kidney disease", "KIDNEY DISEASE", "kidney; damage", "Disorder renal", "Kidney Disease", "Renal Diseases", "Renal disorder", "renal diseases", "DISORDER RENAL", "Renal Disorder", "renal disorder", "kidney disease", "renal; disease", "RENAL DISORDER", "kidney disorder", "Disease, Kidney", "Nephropathy NOS", "kidney diseases", "RENAL DISORDERS", "renal disorders", "NEPHROPATHY NOS", "Kidney Disorder", "DISORDER KIDNEY", "Kidney disorder", "Kidney Diseases", "Disorder;kidney", "Kidney diseases", "Nephropathy, NOS", "diseases kidneys", "Diseases, Kidney", "Kidney Disorders", "kidney disorders", "Renal disease NOS", "Disease of kidney", "Kidneys--Diseases", "disease of kidney", "Renal disorder NOS", "Renal disease, NOS", "RENAL DISEASE, NOS", "Disorder of kidney", "disorder of kidney", "Kidney disease, NOS", "Renal disorder, NOS", "Renal Disorder, NOS", "nephrologic disease", "nephropathy (diagnosis)", "Kidney disease (disorder)", "renal disease (diagnosis)", "renal disorder (diagnosis)", "kidney disease or disorder", "RENAL DISORDERS: NONSPECIFIC", "disease or disorder of kidney", "impaired renal function disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kidney disorder", "shortest_name_length": 11}
{"curie": "MONDO:0007427", "names": ["deafness with anhidrotic ectodermal dysplasia", "DEAFNESS WITH ANHIDROTIC ECTODERMAL DYSPLASIA", "Deafness with Anhidrotic Ectodermal Dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness with anhidrotic ectodermal dysplasia", "shortest_name_length": 45}
{"curie": "MONDO:0032854", "names": ["ZLS3", "zimmermann-laband syndrome 3", "ZIMMERMANN-LABAND SYNDROME 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "zimmermann-laband syndrome 3", "shortest_name_length": 4}
{"curie": "UMLS:C1266185", "names": ["Diffuse Retinoblastoma", "diffuse retinoblastoma", "Retinoblastoma, diffuse", "diffuse retinoblastoma (diagnosis)", "Retinoblastoma, diffuse (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retinoblastoma, diffuse", "shortest_name_length": 22}
{"curie": "UMLS:C3897512", "names": ["Stage IVB Thyroid Gland Follicular Cancer", "Stage IVB Thyroid Gland Follicular Carcinoma", "Stage IVB Thyroid Gland Follicular Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Thyroid Gland Follicular Carcinoma AJCC v7", "shortest_name_length": 41}
{"curie": "UMLS:C5204259", "names": ["Renal Leiomyoma", "Kidney Leiomyoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kidney Leiomyoma", "shortest_name_length": 15}
{"curie": "MONDO:0002152", "names": ["intermittent squint", "Intermittent squint", "Intermittent tropia", "intermittent heterotropia", "heterotropia intermittent", "Intermittent heterotropia", "Heterotropia, intermittent", "intermittent; heterotropia", "heterotropia; intermittent", "Intermittent tropia (disorder)", "Intermittent heterotropia, NOS", "intermittent heterotropia (diagnosis)", "Unspecified intermittent heterotropia", "Intermittent heterotropia, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intermittent squint", "shortest_name_length": 19}
{"curie": "MONDO:0008946", "names": ["Cerebral Angiopathy, Dysphoric", "CEREBRAL ANGIOPATHY, DYSPHORIC", "cerebral angiopathy, dysphoric"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral angiopathy, dysphoric", "shortest_name_length": 30}
{"curie": "MONDO:0012541", "names": ["LAMM syndrome", "Lamm Syndrome", "DEAFNESS WITH LAMM", "Deafness with Lamm", "deafness with Lamm", "Microdontia-type I microtia-deafness syndrome", "microdontia-type I microtia-deafness syndrome", "Microdontia-type I microtia-hearing loss syndrome", "deafness with labyrinthine aplasia, microtia, and microdontia", "Deafness with labyrinthine aplasia, microtia, and microdontia", "Hearing loss with labyrinthine aplasia, microtia, and microdontia", "Deafness with Labyrinthine Aplasia Microtia and Microdontia (LAMM)", "deafness with labyrinthine aplasia microtia and microdontia (LAMM)", "congenital deafness with inner ear agenesis microtia and microdontia", "deafness congenital with inner ear agenesis microtia and microdontia", "Congenital Deafness with Inner Ear Agenesis, Microtia, and Microdontia", "Congenital deafness with inner ear agenesis, microtia, and microdontia", "deafness, congenital with inner ear agenesis, microtia, and microdontia", "Congenital deafness with labyrinthine aplasia, microtia and microdontia", "Congenital Deafness with Labyrinthine Aplasia, Microtia, and Microdontia", "deafness, congenital, with inner EAR agenesis, microtia, and microdontia", "Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia", "DEAFNESS, CONGENITAL, WITH INNER EAR AGENESIS, MICROTIA, AND MICRODONTIA", "Deafness, Congenital, with Labyrinthine Aplasia, Microtia, and Microdontia", "deafness, congenital, with labyrinthine aplasia, microtia, and microdontia", "DEAFNESS, CONGENITAL, WITH LABYRINTHINE APLASIA, MICROTIA, AND MICRODONTIA", "Congenital deafness with labyrinthine aplasia, microtia and microdontia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness with labyrinthine aplasia, microtia, and microdontia", "shortest_name_length": 13}
{"curie": "MONDO:0008825", "names": ["Illum syndrome", "Illum Syndrome", "ILLUM syndrome", "ILLUM SYNDROME", "Illium syndrome", "arthrogryposis multiplex congenita whistling face", "Arthrogryposis multiplex congenita whistling face", "Arthrogryposis Multiplex Congenita With Whistling Face", "arthrogryposis multiplex congenita-whistling face syndrome", "Arthrogryposis multiplex congenita-whistling face syndrome", "arthrogryposis, whistling face, and developmental retardation", "ARTHROGRYPOSIS, WHISTLING FACE, AND DEVELOPMENTAL RETARDATION", "Arthrogryposis multiplex congenita and whistling face syndrome", "arthrogryposis, whistling face, and developintellectual disability", "Arthrogryposis multiplex congenita and whistling face syndrome (disorder)", "Lethal autosomal recessive arthrogryposis multiplex congenita with whistling face and calcifications of the nervous system", "lethal autosomal recessive arthrogryposis multiplex congenita with whistling face and calcifications of the nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis multiplex congenita-whistling face syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0017558", "names": ["congenital elbow dislocation, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital elbow dislocation, unilateral", "shortest_name_length": 40}
{"curie": "UMLS:C5420336", "names": ["Metastatic Pharyngeal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Pharyngeal Squamous Cell Carcinoma", "shortest_name_length": 45}
{"curie": "MONDO:0002069", "names": ["axillary tail of breast cancer", "cancer of axillary tail of breast", "female breast axillary tail cancer", "malignant axillary tail of breast neoplasm", "malignant neoplasm of axillary tail of breast", "malignant tumor of axillary tail of female breast", "malignant neoplasm of axillary tail of female breast", "Malignant neoplasm of axillary tail of female breast", "Malignant neoplasm of axillary tail of breast, female", "Malignant neoplasm of axillary tail of female breast (disorder)", "malignant neoplasm of axillary tail of female breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "female breast axillary tail cancer", "shortest_name_length": 30}
{"curie": "MONDO:0004757", "names": ["chronic ethmoiditis", "Chronic ethmoiditis", "chronic ethmoid sinusitis", "ethmoid sinusitis, chronic", "Chronic ethmoidal sinusitis", "chronic ethmoidal sinusitis", "Chronic Ethmoidal Sinusitis", "Chronic sinusitis, ethmoidal", "ethmoidal sinusitis - chronic", "Chronic ethmoidal sinusitis (disorder)", "chronic ethmoidal sinusitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic ethmoidal sinusitis", "shortest_name_length": 19}
{"curie": "UMLS:C3266262", "names": ["Multiple chronic diseases", "Multiple Chronic Illnesses", "Chronic Illnesses, Multiple", "Multiple Chronic Conditions", "Chronic Conditions, Multiple", "Multiple Chronic Health Conditions", "Multiple Chronic Medical Conditions", "Multiple chronic diseases (situation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Multiple Chronic Conditions", "shortest_name_length": 25}
{"curie": "MONDO:0003475", "names": ["papillary ependymoma", "Papillary Ependymoma", "Papillary ependymoma", "papillary; ependymoma", "Ependymoma, Papillary", "Papillary Ependymomas", "ependymoma; papillary", "Ependymomas, Papillary", "ependymoma; papillary, unspecified site", "papillary; ependymoma, unspecified site", "Papillary ependymoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papillary ependymoma", "shortest_name_length": 20}
{"curie": "UMLS:C1333264", "names": ["Dedifferentiated Dermatofibrosarcoma Protuberans"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dedifferentiated Dermatofibrosarcoma Protuberans", "shortest_name_length": 48}
{"curie": "UMLS:C2981176", "names": ["Stage I Penile Cancer", "Stage I Penis Cancer AJCC v6", "Penile Cancer Stage I AJCC v6", "Stage I Penile Cancer AJCC v6", "Stage I Penis Carcinoma AJCC v6", "Stage I Penile Carcinoma AJCC v6", "Penile Carcinoma Stage I AJCC v6", "Stage I Carcinoma of Penis AJCC v6", "Stage I Carcinoma of the Penis AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Penile Cancer AJCC v6", "shortest_name_length": 21}
{"curie": "UMLS:C2348347", "names": ["Drug/Toxin-Induced Aplastic Anemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drug/Toxin-Induced Aplastic Anemia", "shortest_name_length": 34}
{"curie": "MONDO:0013006", "names": ["IGHD1B", "IGHD 1B", "IGHD IB", "Dwarfism Of Sindh", "dwarfism of Sindh", "congenital IGHD type IB", "Congenital IGHD type IB", "congenital isolated GH deficiency type IB", "Congenital isolated GH deficiency type IB", "isolated growth hormone deficiency type IB", "Isolated growth hormone deficiency type IB", "isolated growth hormone deficiency type 1B", "isolated Growth hormone deficiency, type 1B", "Isolated Growth Hormone Deficiency, Type IB", "ISOLATED GROWTH HORMONE DEFICIENCY, TYPE IB", "isolated growth hormone deficiency, type IB", "growth hormone deficiency, isolated, type IB", "congenital isolated growth hormone deficiency type IB", "Congenital isolated growth hormone deficiency type IB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated growth hormone deficiency type IB", "shortest_name_length": 6}
{"curie": "MONDO:0019432", "names": ["rheumatoid factor-negative JIA", "polyarthritis without rheumatoid factor", "juvenile rheumatoid factor-negative polyarthritis", "rheumatoid factor-negative juvenile idiopathic arthritis", "polyarticular juvenile idiopathic arthritis, rheumatoid factor negative"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rheumatoid factor-negative juvenile idiopathic arthritis", "shortest_name_length": 30}
{"curie": "MONDO:0024466", "names": ["HCFP1", "MBS2, FORMERLY", "Mobius syndrome 2", "Moebius syndrome 2", "MOBIUS SYNDROME 2, FORMERLY", "Mobius syndrome 2, formerly", "Moebius syndrome 2, formerly", "MOEBIUS SYNDROME 2, FORMERLY", "FACIAL PARESIS, HEREDITARY CONGENITAL, 1", "facial paresis, hereditary congenital, 1", "FACIAL PARESIS, HEREDITARY, CONGENITAL HCFP1", "facial palsy, congenital, unilateral or bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "facial paresis, hereditary congenital, 1", "shortest_name_length": 5}
{"curie": "MONDO:0004198", "names": ["solid pattern testicular yolk sac tumor", "Testicular Yolk Sac Tumor, Solid Pattern", "testicular yolk sac tumor, solid pattern"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular yolk sac tumor, solid pattern", "shortest_name_length": 39}
{"curie": "MONDO:0002800", "names": ["thrombophlebitis", "Thrombophlebitis", "THROMBOPHLEBITIS", "Thrombophlebitides", "Thrombophlebitis NOS", "Thrombophlebitis, NOS", "Venous thrombophlebitis", "Thrombophlebitis (disorder)", "thrombophlebitis (diagnosis)", "Thrombophlebitis leg superficial", "THROMBOPHLEBITIS LEG SUPERFICIAL", "thrombophlebitis; leg, superficial", "Superficial thrombophlebitis of leg", "superficial thrombophlebitis of leg", "Thrombophlebitis of a superficial leg vein", "thrombophlebitis of a superficial leg vein", "LOWER EXTREMITY THROMBOPHLEBITIS SUPERFICIAL", "lower extremity; thrombophlebitis, superficial (vessels)", "Thrombophlebitis of superficial veins of lower extremity", "thrombophlebitis of superficial veins of lower extremity", "thrombophlebitis; lower extremity, superficial (vessels)", "thrombophlebitis of superficial vessels of lower extremity", "Thrombophlebitis of superficial veins of lower extremity (disorder)", "thrombophlebitis of superficial vessels of lower extremity (diagnosis)", "Phlebitis and thrombophlebitis of superficial vessels of lower extremities", "phlebitis and thrombophlebitis of superficial vessels of lower extremities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombophlebitis", "shortest_name_length": 16}
{"curie": "MONDO:0012324", "names": ["FRIAS SYNDROME", "Frias syndrome", "Del(14)(q22q23)", "monosomy 14q22q23", "Monosomy 14q22q23", "monosomy 14q22-q23", "Monosomy 14q22-q23", "14q22q23 microdeletion syndrome", "14q22-q23 microdeletion syndrome", "chromosome 14Q22 deletion syndrome", "CHROMOSOME 14q22 DELETION SYNDROME", "14q22q23 microdeletion syndrome (disorder)", "GROWTH DEFICIENCY, FACIAL ANOMALIES, AND BRACHYDACTYLY", "Growth Deficiency, Facial Anomalies, And Brachydactyly", "Growth deficiency, Facial anomalies, and brachydactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Frias syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0011671", "names": ["HDL2", "Huntington Disease-Like 2", "HUNTINGTON DISEASE-LIKE 2", "Huntington disease-like 2", "Huntington's disease-like 2", "Huntington disease-like type 2", "Huntington disease-like 2 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Huntington disease-like 2", "shortest_name_length": 4}
{"curie": "MONDO:0015466", "names": ["Currarino disease", "cranio osteoarthropathy", "cranio-osteoarthropathy", "Reginato-Schiapachasse syndrome", "Reginato Schiapachasse syndrome", "Currarino idiopathic osteoarthropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cranio-osteoarthropathy", "shortest_name_length": 17}
{"curie": "UMLS:C5206941", "names": ["Primary peritoneal carcinosarcoma", "Primary Peritoneal Carcinosarcoma", "Primary Peritoneal Malignant Mixed Mesodermal (Mullerian) Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary peritoneal carcinosarcoma", "shortest_name_length": 33}
{"curie": "UMLS:C1276146", "names": ["Skin Lymphoma", "Lymphoma cutis", "LYMPHOMA CUTIS", "Cutaneous lymphoma", "lymphoma cutaneous", "cutaneous lymphoma", "Cutaneous Lymphoma", "lymphoma; cutaneous", "cutaneous lymphomas", "cutaneous; lymphoma", "Cutaneous lymphoma, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous lymphoma", "shortest_name_length": 13}
{"curie": "UMLS:C4525739", "names": ["Stage IIIA Colorectal Neuroendocrine Tumor", "Stage IIIA Colorectal Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Colorectal Neuroendocrine Tumor AJCC v8", "shortest_name_length": 42}
{"curie": "MONDO:0004518", "names": ["anterior urethra cancer", "anterior urethral cancer", "anterior urethra malignant tumor", "Anterior Urethra Malignant Tumor", "anterior urethral malignant tumor", "Anterior Urethral Malignant Tumor", "Anterior urethral malignant tumor", "anterior urethra malignant neoplasm", "Anterior Urethra Malignant Neoplasm", "Malignant Tumor of Anterior Urethra", "malignant tumor of anterior urethra", "anterior urethral malignant neoplasm", "Anterior Urethral Malignant Neoplasm", "Malignant Neoplasm of Anterior Urethra", "malignant neoplasm of anterior urethra", "malignant tumor of the anterior urethra", "Malignant Tumor of the Anterior Urethra", "malignant neoplasm of the anterior urethra", "Malignant Neoplasm of the Anterior Urethra"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anterior urethra cancer", "shortest_name_length": 23}
{"curie": "MONDO:0004865", "names": ["blue drum syndrome", "Blue drum syndrome", "acute mucoid otitis media", "Acute mucoid otitis media", "otitis; media, mucoid, acute", "otitis; media, acute, mucoid", "Acute mucoid otitis media (disorder)", "acute mucoid otitis media (diagnosis)", "acute non-suppurative otitis media - mucoid", "Acute non-suppurative otitis media - mucoid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blue drum syndrome", "shortest_name_length": 18}
{"curie": "UMLS:C3274273", "names": ["TAPVR Type I", "Type I Total Anomalous Pulmonary Venous Return", "Type I (Supracardiac) Total Anomalous Pulmonary Venous Return", "Total Anomalous Pulmonary Venous Return, Type I (Supracardiac)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Type I Total Anomalous Pulmonary Venous Return", "shortest_name_length": 12}
{"curie": "UMLS:C1304177", "names": ["idiopathic angioedema", "Idiopathic angioedema", "Idiopathic angio-oedema", "Idiopathic angioedema (disorder)", "idiopathic angioedema (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Idiopathic angioedema", "shortest_name_length": 21}
{"curie": "UMLS:C0553558", "names": ["Jackknife Seizure", "Jackknife Seizures", "Seizure, Jackknife", "Seizures, Jackknife"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jackknife Seizures", "shortest_name_length": 17}
{"curie": "UMLS:C4764052", "names": ["Refractory WHO Grade 2 Glioma", "Refractory WHO Grade II Glioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory WHO Grade 2 Glioma", "shortest_name_length": 29}
{"curie": "MONDO:0016649", "names": ["WARBM", "micro syndrome", "Warburg micro syndrome", "Warburg-Sjo-Fledelius syndrome", "microcephaly, microcornea, congenital cataract, mental retardation, optic atrophy and hypogenitalism", "microcephaly, microcornea, congenital cataract, intellectual disability, optic atrophy and hypogenitalism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Warburg micro syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0015733", "names": ["low anorectal malformation", "Low Anorectal Malformation", "Low anorectal malformation", "Low anorectal malformation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "low anorectal malformation", "shortest_name_length": 26}
{"curie": "UMLS:C5204283", "names": ["Diffuse Large B-Cell Lymphoma in Complete Remission"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse Large B-Cell Lymphoma in Complete Remission", "shortest_name_length": 51}
{"curie": "MONDO:0021669", "names": ["Post-Infection Syndrome", "Postinfectious disorder", "Post Infection Syndrome", "Syndrome, Post-Infection", "Post-infectious disorder", "Post Infectious Disorder", "post-infectious disorder", "Post-Infection Syndromes", "Post-Infectious Disorder", "Post-Infectious Disorders", "Post Infectious Disorders", "sequela of infectious disorder", "Post-Infectious Disease Syndrome", "Post Infectious Disease Syndrome", "Syndrome, Post-Infectious Disease", "Post-Infectious Disease Syndromes", "Post-infectious disorder (disorder)", "Post Active Phase of Infection Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "post-infectious disorder", "shortest_name_length": 23}
{"curie": "MONDO:0002929", "names": ["Immature lungs", "failure; expansion", "Primary atelectasis", "atelectasis; primary", "Pulmonary immaturity", "primary; atelectasis", "pulmonary immaturity", "pulmonary; immaturity", "immaturity; pulmonary", "Pulmonary immaturity NOS", "Pulmonary immaturity, NOS", "newborn; atelectasis, primary", "Primary atelectasis of newborn", "primary atelectasis of newborn", "atelectasis; fetus or newborn, primary", "primary atelectasis of fetus or newborn", "Primary atelectasis, in perinatal period", "pulmonary immaturity of fetus or newborn", "primary atelectasis, in perinatal period", "Primary atelectasis, NOS, in perinatal period", "Primary atelectasis, in perinatal period (disorder)", "primary atelectasis of fetus or newborn (diagnosis)", "pulmonary immaturity of fetus or newborn (diagnosis)", "Primary failure to expand terminal respiratory units"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary immaturity", "shortest_name_length": 14}
{"curie": "MONDO:0018844", "names": ["urachal cyst", "urachus cyst", "Urachal cyst", "Urachal Cyst", "Urachal Cysts", "Cyst, Urachal", "URACHUS, CYST", "urachal cysts", "cyst; urachus", "urachus; cyst", "Cysts, Urachal", "allantoic cyst", "Allantoic cyst", "Cyst of urachus", "urachal cyst (disease)", "Congenital urachal cyst", "Congenital cyst of urachus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urachal cyst", "shortest_name_length": 12}
{"curie": "MONDO:0042485", "names": ["septic arthritis", "Septic Arthritis", "infective arthritis", "Infective Arthritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infective arthritis", "shortest_name_length": 16}
{"curie": "UMLS:C5418775", "names": ["Recurrent Primary Peritoneal Transitional Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Primary Peritoneal Transitional Cell Carcinoma", "shortest_name_length": 56}
{"curie": "UMLS:C0920195", "names": ["Aphakic cystoid macular edema", "Aphakic cystoid macular oedema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aphakic cystoid macular edema", "shortest_name_length": 29}
{"curie": "MONDO:0043152", "names": ["RF-ve CP", "negative rheumatoid factor polyarthritis", "Negative rheumatoid factor polyarthritis", "Rheumatoid factor-negative polyarthritis", "rheumatoid factor-negative polyarthritis", "Rheumatoid factor negative erosive chronic polyarthritis", "rheumatoid factor negative erosive chronic polyarthritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "negative rheumatoid factor polyarthritis", "shortest_name_length": 8}
{"curie": "MONDO:0014208", "names": ["CMT2R", "Charcot-Marie-Tooth disease type 2R", "Charcot-Marie-Tooth disease, type 2R", "Charcot-Marie-Tooth neuropathy type 2R", "Charcot-Marie-Tooth neuropathy, type 2R", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2R", "TRIM2 Charcot-Marie-Tooth disease type 2", "Charcot-Marie-Tooth disease, axonal, type 2R", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R", "Charcot-Marie-Tooth disease type 2R (disorder)", "Charcot-Marie-Tooth disease type 2R (diagnosis)", "autosomal recessive axonal Charcot-Marie-Tooth disease type 2R", "Charcot-Marie-Tooth disease type 2 caused by mutation in TRIM2", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2R", "Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2R"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 2R", "shortest_name_length": 5}
{"curie": "UMLS:C2983711", "names": ["Gallbladder Cancer by AJCC v6 Stage", "Gallbladder Carcinoma by AJCC v6 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gallbladder Cancer by AJCC v6 Stage", "shortest_name_length": 35}
{"curie": "MONDO:0006488", "names": ["vaginal carcinosarcoma", "Vaginal Carcinosarcoma", "vaginal malignant mixed Mullerian tumor", "Vaginal Mixed Epithelial and Mesenchymal Tumor", "vaginal mixed epithelial and mesenchymal tumor", "Vaginal Mixed Epithelial and Mesenchymal Neoplasm", "vaginal malignant mixed mesodermal (mullerian) tumor", "vaginal malignant mixed mesodermal (Mullerian) tumor", "vaginal malignant mixed mesodermal (Müllerian) tumor", "Vaginal Malignant Mixed Mesodermal (Müllerian) Tumor", "Vaginal Malignant Mixed Mesodermal (Mullerian) Tumor", "malignant vaginal mixed epithelial and mesenchymal tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vaginal carcinosarcoma", "shortest_name_length": 22}
{"curie": "MONDO:0002135", "names": ["optic neuropathy", "Optic neuropathy", "neuropathy optic", "Optic Neuropathy", "Neuropathy, Optic", "Optic Neuropathies", "optic neuropathies", "n.opticus; disorder", "Optic Nerve Disease", "optic nerve disease", "disease nerve optic", "optic nerve disorder", "Optic Nerve Diseases", "Optic nerve disorder", "Optic Nerve Disorder", "diseases nerve optic", "optic nerve diseases", "optic nerve disorders", "Optic Nerve Disorders", "disorders nerve optic", "diseases nerves optic", "Neural Optical Lesion", "Neural-Optical Lesion", "optic nerve; disorder", "Optic nerve--Diseases", "disorders nerves optic", "Neural-Optical Lesions", "Lesion, Neural-Optical", "Disorder of optic nerve", "disorder of optic nerve", "cranial nerve II disease", "Optic nerve disorder NOS", "Cranial Nerve II Diseases", "Cranial Nerve II Disorder", "disease of cranial nerve II", "Disorder of cranial nerve 2", "Disorder of the optic nerve", "Disorder of optic nerve, NOS", "disorder of the second nerve", "DISORDERS OF THE OPTIC NERVE", "disorder of cranial nerve II", "Second Cranial Nerve Diseases", "Second cranial nerve disorder", "Second Cranial Nerve Disorder", "second cranial nerve disorder", "Optic nerve disease or syndrome", "Disorder of second cranial nerve", "optic nerve disorders (diagnosis)", "Disorder of optic nerve (disorder)", "disease (or disorder); optic nerve", "disease (or disorder); nerve, optic", "cranial nerve II disease or disorder", "CRANIAL NERVE II OPTIC NERVE DISORDER", "disease or disorder of cranial nerve II", "cranial nerve; disorder, second (optic)", "Second cranial nerve disorder or syndrome", "disease (or disorder); cranial nerve, second (optic)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "optic nerve disorder", "shortest_name_length": 16}
{"curie": "MONDO:0005438", "names": ["lymph node metastasis", "Lymph Node Metastases", "Lymph Node Metastasis", "lymph node metastases", "lymph metastases node", "Lymph node metastases", "LYMPH NODE METASTASIS", "lymph metastasis nodes", "lymph metastases nodes", "Metastasis, Lymph Node", "metastasis to lymph node", "Metastasis to lymph node", "Metastasis to Lymph Node", "Metastases to Lymph Nodes", "metastases to lymph nodes", "Metastases to lymph nodes", "Secondary lymph node cancer", "cancer lymph nodes secondary", "metastatic tumor to lymph node", "Metastatic Tumor to Lymph Node", "lymph node metastatic carcinoma", "Cancer metastatic to lymph nodes", "Secondary malignancy of lymph nodes", "metastatic neoplasm to the lymph node", "Metastatic Neoplasm to the Lymph Node", "lymph node neoplasm malignant secondary", "Secondary malignant neoplasm of lymph node", "Metastatic Malignant Neoplasm in Lymph Node", "Metastatic malignant neoplasm of lymph node", "Metastatic malignant neoplasm to lymph node", "secondary malignant neoplasm of lymph nodes", "Secondary malignant neoplasm of lymph node, NOS", "metastasis of malignant neoplasm to lymph nodes", "Metastatic Malignant Neoplasm to the Lymph Nodes", "metastatic malignant neoplasm in the lymph nodes", "Metastatic malignant neoplasm to lymph node, NOS", "metastatic malignant neoplasm to the lymph nodes", "Metastatic Malignant Neoplasm in the Lymph Nodes", "Metastatic malignant neoplasm to lymph node (disorder)", "secondary malignant neoplasm of lymph nodes (diagnosis)", "Secondary and unspecified malignant neoplasm of lymph nodes", "metastasis of malignant neoplasm to lymph nodes (diagnosis)", "Secondary and unspecified malignant neoplasm of lymph nodes NOS", "Secondary and unspecified malignant neoplasm of lymph node, unspecified", "Secondary and unspecified malignant neoplasm of lymph nodes, site unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metastatic malignant neoplasm in the lymph nodes", "shortest_name_length": 21}
{"curie": "MONDO:0000721", "names": ["Xanthinuria", "XANTHINURIA", "xanthinuria", "Classic xanthinuria", "Xanthic urolithiasis", "Xanthinuria (disorder)", "Xanthine stone disease", "Hereditary xanthinuria", "xanthinuria (diagnosis)", "xanthinuria; hereditary", "Increased urinary xanthine", "Hereditary xanthinuria, NOS", "Hereditary xanthinuria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "xanthinuria", "shortest_name_length": 11}
{"curie": "MONDO:0019940", "names": ["haff", "hypertrichosis-coarse face syndrome", "acromegaloid hypertrichosis syndrome", "hypertrichosis-acromegaloid facial features syndrome", "hypertrichosis-acromegaloid facial appearance syndrome", "acromegaloid facial appearance syndrome and hypertrichosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrichosis-acromegaloid facial appearance syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C5237041", "names": ["Recurrent Endometrioid Primary Peritoneal Carcinoma", "Recurrent Primary Peritoneal Endometrioid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Primary Peritoneal Endometrioid Adenocarcinoma", "shortest_name_length": 51}
{"curie": "MONDO:0014049", "names": ["UFS2", "UROFACIAL SYNDROME 2", "urofacial syndrome 2", "LRIG2 Ochoa syndrome", "urofacial syndrome type 2", "Ochoa syndrome caused by mutation in LRIG2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urofacial syndrome 2", "shortest_name_length": 4}
{"curie": "MONDO:0003025", "names": ["conventional angiosarcoma", "Conventional Angiosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "conventional angiosarcoma", "shortest_name_length": 25}
{"curie": "MONDO:0024549", "names": ["MCOPCB1", "microphthalmia with coloboma 1", "Microphthalmia, Colobomatous, Isolated 1", "MICROPHTHALMIA, COLOBOMATOUS, ISOLATED 1", "microphthalmia, colobomatous, isolated 1", "microphthalmia, isolated, with coloboma 1", "Microphthalmia, Isolated, with Coloboma 1", "MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microphthalmia with coloboma 1", "shortest_name_length": 7}
{"curie": "MONDO:0003669", "names": ["seminoma", "SEMINOMA", "Seminoma", "Seminomas", "seminomas", "Seminoma NOS", "Seminoma, NOS", "Seminoma, Pure", "seminoma testis", "testis seminoma", "Seminoma testis", "TESTIS, SEMINOMA", "Seminoma of Testis", "seminoma of testis", "Seminoma of testis", "Malignant seminoma", "SEMINOMA OF TESTIS", "Seminoma (disorder)", "Testicular Seminoma", "testicular seminoma", "TESTICULAR SEMINOMA", "Testicular seminoma", "SEMINOMA, MALIGNANT", "seminoma, testicular", "seminoma (diagnosis)", "Seminoma of the Testis", "seminoma of the testis", "testis cancer, seminoma", "Testicular Seminoma Pure", "testicular Seminoma Pure", "testicular seminoma Pure", "testicle cancer, seminoma", "seminoma testicular cancer", "Testicular seminoma (pure)", "malignant neoplasm seminoma", "testicular cancer, seminoma", "Testicular seminoma pure NOS", "testicular seminoma (disease)", "Seminoma of testis (disorder)", "seminoma of testis (diagnosis)", "Seminomatous germ cell tumor of testis", "seminomatous germ cell tumor of testis", "testicular seminomatous germ cell tumor", "Testicular seminomatous germ cell tumor", "Malignant seminoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular seminoma", "shortest_name_length": 8}
{"curie": "MONDO:0016820", "names": ["MYMY", "MOYAMOYA", "moyamoya", "Moyamoya", "moya disease", "moyamoya disease", "disease moyamoya", "Moyamoya disease", "Moyamoya Disease", "MOYAMOYA DISEASE", "moya-moya disease", "Moyamoya Syndrome", "moyamoya; disease", "moya moya disease", "moyamoya syndrome", "disease moya moya", "Moyamoya syndrome", "Moya-Moya Disease", "Moya Moya Disease", "Disease, Moya-Moya", "Moyamoya disease, primary", "Moyamoya disease (disorder)", "Moyamoya disease, secondary", "Idiopathic Moyamoya disease", "idiopathic Moyamoya disease", "Moyamoya disease (diagnosis)", "disease (or disorder); moyamoya", "Cerebrovascular Moyamoya Disease", "CEREBROVASCULAR MOYAMOYA DISEASE", "Progressive intracranial arterial occlusion", "progressive intracranial arterial occlusion", "Spontaneous occlusion of the circle of Willis", "Progressive intracranial arterial occlusion syndrome", "Progressive intracranial arterial occlusion (disorder)", "Progressive Intracranial Occlusive Arteropathy (Moyamoya)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Moyamoya disease", "shortest_name_length": 4}
{"curie": "UMLS:C5557317", "names": ["DS Stage IIIB Plasma Cell Myeloma", "Durie/Salmon Stage IIIB Plasma Cell Myeloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DS Stage IIIB Plasma Cell Myeloma", "shortest_name_length": 33}
{"curie": "UMLS:C0043345", "names": ["Dry skin", "xeroderma", "XERODERMA", "Xeroderma", "Xerodermia", "Xerodermas", "xerodermia", "Xeroderma, NOS", "Anhydrotic skin", "Xerodermia, NOS", "Xeroderma (disorder)", "xeroderma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Xeroderma", "shortest_name_length": 8}
{"curie": "UMLS:C5555875", "names": ["Transformed B-Cell Lymphoma, Unclassifiable, with Features Intermediate between Diffuse Large B-Cell Lymphoma and Classic Hodgkin Lymphoma to Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transformed B-Cell Lymphoma, Unclassifiable, with Features Intermediate between Diffuse Large B-Cell Lymphoma and Classic Hodgkin Lymphoma to Diffuse Large B-Cell Lymphoma", "shortest_name_length": 171}
{"curie": "UMLS:C5555080", "names": ["Secondary Peripheral Chondrosarcoma, Grade 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary Peripheral Chondrosarcoma, Grade 2", "shortest_name_length": 44}
{"curie": "UMLS:C4683416", "names": ["Differentiated Thyroid Gland Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Differentiated Thyroid Gland Carcinoma by AJCC v8 Stage", "shortest_name_length": 55}
{"curie": "MONDO:0032665", "names": ["MRT68", "Mental Retardation, Autosomal Recessive 68", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 68", "autosomal recessive intellectual developmental disorder 68", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 68", "intellectual developmental disorder, autosomal recessive 68"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder, autosomal recessive 68", "shortest_name_length": 5}
{"curie": "MONDO:0001563", "names": ["auditory; nerve", "acoustic nerve disease", "acoustic nerve disorder", "Auditory nerve disorder", "Acoustic Nerve Disorder", "disorder of eighth nerve", "Auditory nerve disorders", "Disorder of eighth nerve", "auditory nerve; disorder", "Disorder of auditory nerve", "Disorder of acoustic nerve", "disorder of acoustic nerve", "Disorders of acoustic nerve", "Acoustic nerve disorder NOS", "Disorder of cranial nerve 8", "Cranial Nerve VIII Diseases", "acoustic nerve disorder NOS", "Eight cranial nerve disorder", "Cranial Nerve VIII Disorders", "Eighth Cranial Nerve Diseases", "Disorder of eighth nerve, NOS", "VIIIth cranial nerve disorders", "vestibulocochlear nerve disease", "Disorder of acoustic nerve, NOS", "DISORDERS OF THE ACOUSTIC NERVE", "n.vestibulocochlearis; disorder", "Vestibulocochlear Nerve Disease", "vestibulocochlear nerve disorder", "vestibulocochlear nerve diseases", "Vestibulocochlear Nerve Diseases", "Vestibulocochlear Nerve Disorder", "Disorder of eighth cranial nerve", "disorder; vestibulocochlear nerve", "Auditory nerve disease or syndrome", "disease of vestibulocochlear nerve", "disorder of acoustovestibular nerve", "Disorder of vestibulocochlear nerve", "Disorder of acoustovestibular nerve", "disorder of vestibulocochlear nerve", "disturbance; vestibulocochlear nerve", "Disorder of acoustic or eighth nerve", "Disorder of acoustic nerve (disorder)", "disorder of acoustic nerve (diagnosis)", "disease (or disorder); nerve, auditory", "disease (or disorder); nerve, acoustic", "disorder of the vestibulocochlear nerve", "Disorder of the vestibulocochlear nerve", "Eighth cranial nerve disease or syndrome", "cranial nerve; disorder, eighth (auditory)", "vestibulocochlear nerve disease or disorder", "Disorder of the vestibulocochlear nerve, NOS", "disease or disorder of vestibulocochlear nerve", "Acoustic nerve disorder, NOS (see also section X)", "disease (or disorder); cranial nerve, eighth (auditory)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vestibulocochlear nerve disorder", "shortest_name_length": 15}
{"curie": "MONDO:0008386", "names": ["RGS", "Rgs", "RIEG", "Rieg", "RIEG1", "Rieger syndrome type 1", "Rieger Syndrome Type 1", "Rieger Syndrome, Type 1", "RIEGER SYNDROME, TYPE 1", "Rieger syndrome, type 1", "PITX2 Axenfeld-Rieger syndrome", "Axenfeld-Rieger syndrome Type 1", "Axenfeld-Rieger syndrome type 1", "AXENFELD-RIEGER SYNDROME, TYPE 1", "Axenfeld-Rieger syndrome, type 1", "Axenfeld-Rieger Syndrome, Type 1", "Axenfeld-Rieger syndrome Type 1 (diagnosis)", "Axenfeld-Rieger syndrome caused by mutation in PITX2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Axenfeld-Rieger syndrome type 1", "shortest_name_length": 3}
{"curie": "UMLS:C1167735", "names": ["Small Intestine Cancer Stage I", "Stage I Small Intestinal Cancer", "Stage I Small Intestine Carcinoma", "Small intestine carcinoma stage I", "Stage I Small Intestinal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small intestine carcinoma stage I", "shortest_name_length": 30}
{"curie": "UMLS:C5204296", "names": ["Lymphoepithelioma-Like Carcinoma of the Penis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoepithelioma-Like Carcinoma of the Penis", "shortest_name_length": 45}
{"curie": "UMLS:C5418778", "names": ["Recurrent Fallopian Tube Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Fallopian Tube Adenocarcinoma", "shortest_name_length": 39}
{"curie": "UMLS:C0022411", "names": ["Arthrolith", "Joint body", "joint mice", "body joint", "Joint mice", "mice; joint", "Joint mouse", "body joints", "joint mouse", "bodies joints", "Joint;loose body", "Joint Loose Body", "body joints loose", "loose body; joint", "Loose Body, Joint", "joint; loose body", "Loose body, joint", "Joint Loose Bodies", "loose; bodies joint", "Loose Body in Joint", "Loose Bodies, Joint", "Loose body in joint", "loose body in joint", "bodies; loose, joint", "Free bodies in joint", "Corpora libra in joint", "Intra-articular loose body", "Melon seed bodies in joint", "loose bodies (mice) in joint", "Loose body in joint (disorder)", "Loose body in unspecified joint", "Loose body in joint, site unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joint Loose Bodies", "shortest_name_length": 10}
{"curie": "UMLS:C1168200", "names": ["Stage IVB Gallbladder Cancer", "stage IVB gallbladder cancer", "gallbladder cancer stage IVB", "gallbladder carcinoma stage IVB", "Stage IVB Gallbladder Carcinoma", "stage IVB carcinoma of gallbladder", "Gallbladder Cancer Stage IVB AJCC v7", "Stage IVB Gallbladder Cancer AJCC v7", "stage IVB gallbladder cancer AJCC v7", "stage IVB carcinoma of the gallbladder", "Gallbladder Carcinoma Stage IVB AJCC v7", "Stage IVB Gallbladder Carcinoma AJCC v7", "Stage IVB Carcinoma of Gallbladder AJCC v7", "Stage IVB Carcinoma of the Gallbladder AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Gallbladder Carcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0015292", "names": ["endotheliitis", "endothelium inflammation", "inflammation of endothelium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endotheliitis", "shortest_name_length": 13}
{"curie": "MONDO:0022572", "names": ["bilateral renal agenesis dominant type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bilateral renal agenesis dominant type", "shortest_name_length": 38}
{"curie": "UMLS:C5418305", "names": ["Left-Sided Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Left-Sided Breast Carcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0017732", "names": ["alpha-mannosidosis, infantile form", "lysosomal alpha-D-mannosidase deficiency, infantile form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alpha-mannosidosis, infantile form", "shortest_name_length": 34}
{"curie": "MONDO:0001841", "names": ["uterine corpus epithelioid leiomyoma", "Uterine Corpus Epithelioid Leiomyoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine corpus epithelioid leiomyoma", "shortest_name_length": 36}
{"curie": "MONDO:0013802", "names": ["ICRD", "Infantile cerebellar-retinal degeneration", "INFANTILE CEREBELLAR-RETINAL DEGENERATION", "infantile cerebellar retinal degeneration", "infantile cerebellar-retinal degeneration", "Infantile cerebellar and retinal degeneration", "Infantile cerebellar and retinal degeneration (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile cerebellar-retinal degeneration", "shortest_name_length": 4}
{"curie": "MONDO:0002998", "names": ["Skull Base Meningioma", "skull base meningioma", "Meningioma of Skull Base", "meningioma of skull base", "Meningioma of the Skull Base", "meningioma of the skull base", "meningioma of the Skull Base", "basicranium meningioma (disease)", "meningioma (disease) of basicranium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skull base meningioma", "shortest_name_length": 21}
{"curie": "MONDO:0016432", "names": ["heart-hand syndrome", "atriodigital dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heart-hand syndrome", "shortest_name_length": 19}
{"curie": "MONDO:0002897", "names": ["syphilis secondary", "Secondary Syphilis", "Secondary syphilis", "secondary syphilis", "SYPHILIS SECONDARY", "SECONDARY SYPHILIS", "syphilis; secondary", "Syphilis, secondary", "SYPHILIS, SECONDARY", "Secondary syphilis (disorder)", "Unspecified secondary syphilis", "secondary syphilis (diagnosis)", "secondary syphilis of viscera or bone", "Secondary syphilis of viscera or bone", "Secondary syphilis of viscera and bone", "Secondary syphilis of viscera or bone (navigational concept)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary syphilis", "shortest_name_length": 18}
{"curie": "MONDO:0032841", "names": ["USH1M", "Usher syndrome, type 1M", "USHER SYNDROME, TYPE 1M"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Usher syndrome, type 1M", "shortest_name_length": 5}
{"curie": "MONDO:0020694", "names": ["Salivary Gland Epithelial Myoepithelial Carcinoma", "Salivary Gland Epithelial-Myoepithelial Carcinoma", "salivary gland epithelial myoepithelial carcinoma", "epithelial-myoepithelial carcinoma of salivary gland", "biopsy of salivary gland: epithelial-myoepithelial carcinoma", "epithelial-myoepithelial carcinoma of salivary gland (diagnosis)", "biopsy of salivary gland: epithelial-myoepithelial carcinoma (procedure)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "salivary gland epithelial myoepithelial carcinoma", "shortest_name_length": 49}
{"curie": "UMLS:C4528583", "names": ["Stage IIB Breast Cancer", "Prognostic Stage IIB Breast Cancer AJCC v8", "Prognostic Stage IIB Breast Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prognostic Stage IIB Breast Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "MONDO:0000266", "names": ["Lung Aspergillosis", "lung aspergillosis", "Aspergilloses, Lung", "Aspergillosis, Lung", "pulmonary aspergilloma", "Pulmonary Aspergilloses", "Pulmonary aspergillosis", "pulmonary aspergillosis", "aspergillosis pulmonary", "Pulmonary Aspergillosis", "PULMONARY ASPERGILLOSIS", "Aspergillosis, Pulmonary", "Aspergillosis, pulmonary", "Bronchopulmonary Aspergillose", "Pulmonary aspergillus disease", "Bronchopulmonary Aspergillosis", "Aspergillose, Bronchopulmonary", "aspergillosis bronchopulmonary", "Bronchopulmonary aspergillosis", "Bronchopulmonary Aspergilloses", "bronchopulmonary aspergillosis", "Aspergillosis, Bronchopulmonary", "Aspergilloses, Bronchopulmonary", "Pulmonary aspergillosis (disorder)", "Pulmonary aspergillosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary aspergilloma", "shortest_name_length": 18}
{"curie": "UMLS:C0877175", "names": ["Injection site arthritis", "Injection Site Arthritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site arthritis", "shortest_name_length": 24}
{"curie": "MONDO:0025135", "names": ["avian tuberculosis", "Avian Tuberculosis", "Avian Tuberculoses", "tuberculosis avian", "Avian tuberculosis", "Tuberculosis, Avian", "Tuberculoses, Avian", "tuberculosis, avian", "Avian tuberculosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tuberculosis, avian", "shortest_name_length": 18}
{"curie": "MONDO:0100279", "names": ["PEX11B related peroxisome biogenesis disorder", "peroxisome biogenesis disorder due to PEX11B defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder due to PEX11B defect", "shortest_name_length": 45}
{"curie": "UMLS:C1334791", "names": ["CANCER DIFFERENTIATED MODERATELY", "Moderately Differentiated Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Moderately Differentiated Malignant Neoplasm", "shortest_name_length": 32}
{"curie": "MONDO:0008163", "names": ["Ofc Syndrome", "OFC syndrome", "otofaciocervical syndrome", "Fara-Chlupackova syndrome", "Otofaciocervical syndrome", "Otofaciocervical Syndrome", "Fara Chlupackova syndrome", "Otofaciocervical syndrome (disorder)", "otofaciocervical syndrome (diagnosis)", "Familial oto-facio-cervical dysmorphia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "otofaciocervical syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0019169", "names": ["PDH", "PDHC", "PDH Deficiency", "PDH deficiency", "PDH DEFICIENCY", "PDHC Deficiency", "Deficiency, PDH", "Deficiency, PDHC", "PDHC Deficiency Disease", "Ataxia with lactic acidosis", "Ataxia with lactic acidosis I", "Deficiency of alpha-carboxylase", "Pyruvate Dehydrogenase Deficiency", "Pyruvate Decarboxylase Deficiency", "Pyruvate dehydrogenase deficiency", "PYRUVATE DECARBOXYLASE DEFICIENCY", "pyruvate dehydrogenase deficiency", "pyruvate decarboxylase deficiency", "Deficiency, Pyruvate Dehydrogenase", "deficiency; pyruvate dehydrogenase", "Deficiency, Pyruvate Decarboxylase", "Deficiency of pyruvic decarboxylase", "deficiency of pyruvic dehydrogenase", "pyruvate; dehydrogenase, deficiency", "dehydrogenase; pyruvate, deficiency", "Deficiency of pyruvic dehydrogenase", "Deficiency of pyruvate decarboxylase", "Deficiency of pyruvate dehydrogenase", "PDH - Pyruvate dehydrogenase deficiency", "Deficiency of alpha-ketoacid carboxylase", "Pyruvate dehydrogenase complex deficiency", "Pyruvate Dehydrogenase Complex Deficiency", "PYRUVATE DEHYDROGENASE COMPLEX DEFICIENCY", "pyruvate dehydrogenase complex deficiency", "Deficiency of pyruvate decarboxylase (disorder)", "pyruvate dehydrogenase complex (PDHC) deficiency", "Deficiency of pyruvate dehydrogenase (cytochrome)", "Pyruvate Dehydrogenase Complex Deficiency Disease", "pyruvate dehydrogenase complex deficiency disease", "Pyruvate dehydrogenase complex deficiency (disorder)", "Ataxia, Intermittent, with Abnormal Pyruvate Metabolism", "ATAXIA, INTERMITTENT, WITH ABNORMAL PYRUVATE METABOLISM", "Intermittent Ataxia with Pyruvate Dehydrogenase Deficiency", "ATAXIA, INTERMITTENT, WITH PYRUVATE DEHYDROGENASE DEFICIENCY", "Ataxia, Intermittent, with Pyruvate Dehydrogenase, or Decarboxylase, Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyruvate dehydrogenase deficiency", "shortest_name_length": 3}
{"curie": "UMLS:C5420052", "names": ["Intermediate Sinonasal Soft Tissue Neoplasm", "Sinonasal Intermediate Soft Tissue Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intermediate Sinonasal Soft Tissue Neoplasm", "shortest_name_length": 43}
{"curie": "UMLS:C2828182", "names": ["stage I gestational trophoblastic tumor", "Stage I Gestational Trophoblastic Tumor", "stage I gestational trophoblastic tumor AJCC v7", "Stage I Gestational Trophoblastic Tumor AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Gestational Trophoblastic Tumor AJCC v7", "shortest_name_length": 39}
{"curie": "MONDO:0009108", "names": ["dibasic aminoaciduria 1", "dibasic amino aciduria I", "Dibasic Amino Aciduria I", "dibasic amino aciduria 1", "DIBASIC AMINO ACIDURIA I", "dibasic amino aciduria type 1", "hyperdibasic aminoaciduria type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperdibasic aminoaciduria type 1", "shortest_name_length": 23}
{"curie": "MONDO:0002936", "names": ["scrotum basal cell carcinoma", "Scrotal Basal Cell Carcinoma", "basal cell scrotal carcinoma", "scrotal basal cell carcinoma", "Basal cell carcinoma of scrotum", "Basal Cell Carcinoma of Scrotum", "basal cell carcinoma of scrotum", "scrotum skin basal cell carcinoma", "Basal Cell Carcinoma of the Scrotum", "basal cell carcinoma of the scrotum", "skin basal cell carcinoma of scrotum", "basal cell carcinoma of scrotum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scrotum basal cell carcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0024566", "names": ["FEB11", "familial febrile seizures 11", "febrile seizures, familial, 11", "FEBRILE SEIZURES, FAMILIAL, 11", "familial febrile convulsions 11", "CONVULSIONS, FAMILIAL FEBRILE, 11", "convulsions, familial febrile, 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "febrile seizures, familial, 11", "shortest_name_length": 5}
{"curie": "MONDO:0002808", "names": ["PSC", "pancreas serous cystadenoma", "pancreatic serous cystadenoma", "Pancreatic Serous Cystadenoma", "Pancreatic serous cystadenoma", "serous cystadenoma of pancreas", "Serous Cystadenoma of Pancreas", "Pancreatic Microcystic Adenoma", "pancreatic microcystic adenoma", "Serous cystadenoma of pancreas", "serous cystadenoma of the pancreas", "Serous Cystadenoma of the Pancreas", "Serous cystadenoma of pancreas (disorder)", "serous cystadenoma of pancreas (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic serous cystadenoma", "shortest_name_length": 3}
{"curie": "MONDO:0004502", "names": ["parapharyngeal meningioma", "Primary Parapharyngeal Meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parapharyngeal meningioma", "shortest_name_length": 25}
{"curie": "UMLS:C2242489", "names": ["Oncologic complication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oncologic complication", "shortest_name_length": 22}
{"curie": "UMLS:C4553581", "names": ["Stage III", "Stage III Uterine Corpus Cancer AJCC v8", "Stage III Uterine (including Endometrial) Cancer", "Stage III Uterine Corpus Carcinoma or Carcinosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Uterine Corpus Cancer AJCC v8", "shortest_name_length": 9}
{"curie": "MONDO:0003975", "names": ["Littre gland carcinoma", "carcinoma of Littré glands", "Carcinoma of Littré Glands", "Carcinoma of Littre Glands", "carcinoma of Littre glands", "carcinoma of LittrC) glands", "male urethral gland carcinoma", "Adenocarcinoma of Littre Glands", "carcinoma of male urethral gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Littre gland carcinoma", "shortest_name_length": 22}
{"curie": "UMLS:C1333775", "names": ["Gastric Juvenile Polyp", "Gastric Retention Polyp"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Juvenile Polyp", "shortest_name_length": 22}
{"curie": "UMLS:C0850705", "names": ["acquired toxoplasmosis", "Toxoplasmosis;acquired", "Adult Acquired Toxoplasmosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Acquired Toxoplasmosis", "shortest_name_length": 22}
{"curie": "UMLS:C1563730", "names": ["Abdominal cryptorchid", "Abdominal cryptorchidism", "Abdominal Cryptorchidism", "Cryptorchidism, Abdominal", "Retained testicle in abdomen", "Undescended testicle in abdomen", "Abdominal cryptorchidism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abdominal Cryptorchidism", "shortest_name_length": 21}
{"curie": "UMLS:C5555708", "names": ["Unresectable Castration-Resistant Prostate Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Castration-Resistant Prostate Carcinoma", "shortest_name_length": 52}
{"curie": "MONDO:0007325", "names": ["choreoathetosis, familial inverted", "CHOREOATHETOSIS, FAMILIAL INVERTED", "Choreoathetosis, Familial Inverted", "infantile choreoathetosis of Fisher", "INFANTILE CHOREOATHETOSIS OF FISHER", "Infantile Choreoathetosis of Fisher"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choreoathetosis, familial inverted", "shortest_name_length": 34}
{"curie": "MONDO:0012261", "names": ["AUTS6", "autism susceptibility 6", "autism, susceptibility to, 6", "AUTISM, SUSCEPTIBILITY TO, 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autism, susceptibility to, 6", "shortest_name_length": 5}
{"curie": "UMLS:C0863188", "names": ["stage III stomach cancer", "Stomach carcinoma stage III", "Gastric carcinoma stage III", "Stage III Carcinoma of Stomach", "Stage III Gastric Cancer AJCC v6", "Stage III Stomach Cancer AJCC v6", "Stomach Cancer Stage III AJCC v6", "Stage III Gastric (Stomach) Cancer", "Stomach Carcinoma Stage III AJCC v6", "Gastric Carcinoma Stage III AJCC v6", "Stage III Gastric Carcinoma AJCC v6", "Stage III Stomach Carcinoma AJCC v6", "Gastric Carcinoma, Stage III AJCC v6", "Stage III Carcinoma of Stomach AJCC v6", "Carcinoma of Stomach Stage III AJCC v6", "Stage III Carcinoma of the Stomach AJCC v6", "Carcinoma of the Stomach Stage III AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Carcinoma of Stomach", "shortest_name_length": 24}
{"curie": "MONDO:0009421", "names": ["hypogonadism, male", "Primary gonadal failure", "Primary male hypogonadism", "Primary Testicular Failure", "Testicular failure primary", "primary testicular failure", "Primary testicular failure", "Primary failure of the testes", "HYPOGONADISM AND TESTICULAR ATROPHY", "hypogonadism and testicular atrophy", "Hypogonadism and Testicular Atrophy", "Male Hypergonadotropic Hypogonadism", "Primary testicular failure (disorder)", "Hypergonadotropic hypogonadism (males)", "primary testicular failure (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadism, male", "shortest_name_length": 18}
{"curie": "MONDO:0006709", "names": ["Main bile duct tumor", "common bile duct tumor", "tumor of common bile duct", "common bile duct neoplasm", "Common Bile Duct Neoplasms", "Neoplasm of common bile duct", "neoplasm of common bile duct", "common bile duct neoplasm (disease)", "Neoplasm of common bile duct (disorder)", "neoplasm of common bile duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "common bile duct neoplasm", "shortest_name_length": 20}
{"curie": "MONDO:0013240", "names": ["MODY10", "maturity-onset diabetes of the young type 10", "MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 10", "maturity-onset diabetes of the young, type 10", "Maturity-onset diabetes of the young, type 10", "maturity-onset diabetes of the young - type 10", "INS maturity-onset diabetes of the young (disease)", "Maturity-onset diabetes of the young, type 10 (disorder)", "maturity-onset diabetes of the young - type 10 (diagnosis)", "maturity-onset diabetes of the young (disease) caused by mutation in INS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maturity-onset diabetes of the young type 10", "shortest_name_length": 6}
{"curie": "UMLS:C0271635", "names": ["Uncomplicated Diabetes", "Diabetes without Complications", "Diabetes without complications", "Uncomplicated Diabetes Mellitus", "DIABETES MELLITUS NOS UNCOMPLICATED", "diabetes mellitus without complication", "Diabetes mellitus without complication", "Diabetes Mellitus without Complications", "Diabetes mellitus without mention of complication", "Diabetes mellitus without complication (disorder)", "diabetes mellitus without complication (diagnosis)", "Unspecified diabetes mellitus without complication", "Unspecified diabetes mellitus without complications"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diabetes mellitus without complication", "shortest_name_length": 22}
{"curie": "MONDO:0011259", "names": ["RP22", "RP 22", "RETINITIS PIGMENTOSA 22", "retinitis pigmentosa 22", "retinitis pigmentosa type 22"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 22", "shortest_name_length": 4}
{"curie": "MONDO:0016179", "names": ["acquired amyloid peripheral neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired amyloid peripheral neuropathy", "shortest_name_length": 38}
{"curie": "MONDO:0014380", "names": ["MCSKS", "MCOPS14", "syndromic microphthalmia 14", "microphthalmia, syndromic 14", "MICROPHTHALMIA, SYNDROMIC 14", "microphthalmia, syndromic type 14", "microphthalmia-coloboma-rhizomelic skeletal dysplasia", "MICROPHTHALMIA/COLOBOMA AND SKELETAL DYSPLASIA SYNDROME", "microphthalmia/coloboma and skeletal dysplasia syndrome", "colobomatous microphthalmia-rhizomelic dysplasia syndrome", "microphthalmia or coloboma with or without rhizomelic skeletal dysplasia", "microphthalmia and coloboma, with or without rhizomelic skeletal dysplasia", "microphthalmia and/or coloboma with or without rhizomelic skeletal dysplasia", "MICROPHTHALMIA AND/OR COLOBOMA WITH OR WITHOUT RHIZOMELIC SKELETAL DYSPLASIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colobomatous microphthalmia-rhizomelic dysplasia syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C5206085", "names": ["Progressive Thyroid Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Progressive Thyroid Carcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0015348", "names": ["leukoencephalopathy with bilateral anterior temporal lobe cysts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukoencephalopathy with bilateral anterior temporal lobe cysts", "shortest_name_length": 63}
{"curie": "MONDO:0013024", "names": ["CTEPH", "Thromboembolic pulmonary hypertension", "CTEPH, DVT-NEGATIVE, SUSCEPTIBILITY TO", "Cteph, Dvt-negative, susceptibility to", "pulmonary hypertension chronic thromboembolic", "Chronic thromboembolic pulmonary hypertension", "chronic thromboembolic pulmonary hypertension", "Thromboembolic pulmonary hypertension (disorder)", "Chronic thromboembolic pulmonary hypertension (diagnosis)", "PULMONARY HYPERTENSION, CHRONIC THROMBOEMBOLIC, WITHOUT DEEP VEIN THROMBOSIS, SUSCEPTIBILITY TO", "pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic thromboembolic pulmonary hypertension", "shortest_name_length": 5}
{"curie": "UMLS:C1708961", "names": ["Mediastinal Thymoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mediastinal Thymoma", "shortest_name_length": 19}
{"curie": "MONDO:0014659", "names": ["ILFS2", "NBAS infantile liver failure", "infantile liver failure syndrome 2", "INFANTILE LIVER FAILURE SYNDROME 2", "Infantile Liver Failure Syndrome 2", "infantile liver failure syndrome type 2", "infantile liver failure caused by mutation in NBAS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile liver failure syndrome 2", "shortest_name_length": 5}
{"curie": "UMLS:C5237760", "names": ["Locally Advanced Primary Malignant Central Nervous System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Primary Malignant Central Nervous System Neoplasm", "shortest_name_length": 66}
{"curie": "MONDO:0017407", "names": ["David syndrome", "deficiency in anterior pituitary function - variable immunodeficiency syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deficiency in anterior pituitary function - variable immunodeficiency syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C0233697", "names": ["obsession", "Obsession", "Obsessions", "obsessions", "obsessional thoughts", "Obsessive rumination", "Obsessional thoughts", "obsessive ruminations", "Obsessional ruminations", "rumination; obsessional", "obsessional; rumination", "obsessions (physical finding)", "Obsessional thoughts (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Obsessions", "shortest_name_length": 9}
{"curie": "UMLS:C4683622", "names": ["Stage A Chronic Lymphocytic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage A Chronic Lymphocytic Leukemia", "shortest_name_length": 36}
{"curie": "MONDO:0026723", "names": ["MRX108", "Mental Retardation, X-Linked 108", "MENTAL RETARDATION, X-LINKED 108", "X-linked intellectual developmental disorder 108", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 108", "intellectual developmental disorder, X-linked 108", "intellectual developmental disorder, X-linked 108, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder, X-linked 108", "shortest_name_length": 6}
{"curie": "MONDO:0006873", "names": ["malnutrition", "Malnutrition", "malnourished", "Deficiency Disease", "deficiency disease", "Deficiency Diseases", "deficiency diseases", "Deficiency diseases", "Disease, Deficiency", "Diseases, Deficiency", "deficiencies disease", "nutritional deficiency disease", "Nutritional deficiency associated condition", "nutritional deficiencies associated condition", "Nutritional deficiency associated condition (disorder)", "nutritional deficiencies associated condition (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nutritional deficiency disease", "shortest_name_length": 12}
{"curie": "MONDO:0006106", "names": ["Benign Smooth Muscle Tumor", "benign smooth muscle tumor", "Benign Tumor of Smooth Muscle", "benign smooth muscle neoplasm", "benign tumor of smooth muscle", "Benign Smooth Muscle Neoplasm", "benign neoplasm of smooth muscle", "Benign Neoplasm of Smooth Muscle", "Benign Tumor of the Smooth Muscle", "benign tumor of the smooth muscle", "Benign Neoplasm of the Smooth Muscle", "benign neoplasm of the smooth muscle", "smooth muscle tissue benign neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign smooth muscle neoplasm", "shortest_name_length": 26}
{"curie": "UMLS:C1332306", "names": ["Anterior Tongue Tumor", "Anterior Tongue Neoplasm", "Tumor of Anterior Tongue", "Neoplasm of Anterior Tongue", "Tumor of the Anterior Tongue", "Neoplasm of the Anterior Tongue", "neoplasm of anterior dorsal surface of tongue", "neoplasm of anterior dorsal surface of tongue (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplasm of anterior dorsal surface of tongue", "shortest_name_length": 21}
{"curie": "UMLS:C4763798", "names": ["Refractory Monomorphic Epitheliotropic Intestinal T-cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Monomorphic Epitheliotropic Intestinal T-cell Lymphoma", "shortest_name_length": 65}
{"curie": "MONDO:0012221", "names": ["NAGA deficiency", "Galb Deficiency", "Naga Deficiency", "schindler disease", "Schindler Disease", "Schindler disease", "disease schindlers", "Alpha-Naga Deficiency", "NAGA deficiency type 1", "NAGA deficiency type 3", "Naga Deficiency, Type I", "NAGA deficiency, type 1", "NAGA DEFICIENCY, TYPE I", "NAGA deficiency, type 3", "Schindler disease type I", "Schindler disease type 1", "Schindler disease type 3", "NAGA DEFICIENCY, TYPE III", "Schindler Disease, Type I", "Schindler disease, type I", "SCHINDLER DISEASE, TYPE I", "Schindler disease, type 1", "NAGA Deficiency, Type III", "Schindler disease, type 3", "SCHINDLER DISEASE, TYPE III", "Schindler Disease, Type III", "Schindler disease, type III", "Alpha-Galactosidase B Deficiency", "neuroaxonal dystrophy, Schindler type", "Neuroaxonal dystrophy, Schindler type", "NEUROAXONAL DYSTROPHY, SCHINDLER TYPE", "Alpha-Galnac Deficiency, Schindler Type", "Neuronal Axonal Dystrophy, Schindler Type", "Alpha-N-acetylgalactosaminidase deficiency", "Alpha-N-Acetylgalactosaminidase Deficiency", "Angiokeratoma Corporis Diffusum-Glycopeptiduria", "NAGA (alpha-N-acetylgalactosaminidase) deficiency", "Alpha-N-acetylgalactosaminidase deficiency type 3", "Alpha-N-acetylgalactosaminidase deficiency type 1", "alpha-N-acetylgalactosaminidase deficiency type 1", "Alpha-N-acetylgalactosaminidase deficiency, type 3", "Alpha-N-acetylgalactosaminidase deficiency, type 1", "alpha-N-acetylgalactosaminidase deficiency, type 1", "Alpha-N-Acetylgalactosaminidase Deficiency, Type I", "ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, TYPE I", "Alpha-N-Acetylgalactosaminidase Deficiency, Type III", "ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, TYPE III", "Alpha-N-acetylgalactosaminidase deficiency (disorder)", "N-acetyl-alpha-D-galactosaminidase deficiency type III", "NAGA (alpha-N-acetylgalactosaminidase) deficiency type 1", "NAGA (alpha-N-acetylgalactosaminidase) deficiency type 3", "Alpha-N-acetylgalactosaminidase deficiency type 3 (disorder)", "Alpha-N-acetylgalactosaminidase deficiency type 1 (disorder)", "Lysosomal Glycoaminoacid Storage Disease-Angiokeratoma Corporis Diffusum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alpha-N-acetylgalactosaminidase deficiency type 1", "shortest_name_length": 15}
{"curie": "MONDO:0002133", "names": ["chronic rheumatic pericarditis", "Chronic rheumatic pericarditis", "Pericarditis;rheumatic;chronic", "rheumatic pericarditis, chronic", "Rheumatic heart disease with pericarditis", "chronic rheumatic pericarditis (diagnosis)", "Chronic rheumatic heart disease with pericarditis", "Chronic pericarditis due to rheumatic heart disease", "Chronic pericarditis due to rheumatic heart disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic rheumatic pericarditis", "shortest_name_length": 30}
{"curie": "UMLS:C4527424", "names": ["Predominantly Diffuse Follicular Lymphoma with 1p36 Deletion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Predominantly Diffuse Follicular Lymphoma with 1p36 Deletion", "shortest_name_length": 60}
{"curie": "MONDO:0005888", "names": ["ornithosis", "ORNITHOSIS", "Ornithoses", "Ornithosis", "Psittacosis", "PSITTACOSIS", "psittacosis", "Psittacoses", "parrot fever", "PARROT FEVER", "Parrot fever", "FEVER, PARROT", "PNEUMONIA, BEDSONIA", "Ornithosis (disorder)", "psittacosis (diagnosis)", "Ornithosis, unspecified", "Chlamydia psittaci infection", "Parrot fever due to Chlamydia psitacci"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ornithosis", "shortest_name_length": 10}
{"curie": "UMLS:C4330724", "names": ["Multiple Vascular Disruption Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Multiple Vascular Disruption Syndrome", "shortest_name_length": 37}
{"curie": "UMLS:C5395080", "names": ["Acute Myeloid Leukemia, CBFB-MYH11", "Acute Myeloid Leukemia, CBF-beta/MYH11", "Acute myeloid leukemia, CBF-beta/MYH11", "Acute Myeloid Leukemia with Abnormal Marrow Eosinophils", "AML with inv(16)(p13.1q22) or t(16;16)(p13.1;q22); CBFB-MYH11", "AML with inv(16)(p13q22) or t(16;16) (p13.1;q22), (CBFB/MYH11)", "AML with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)", "Acute myeloid leukemia with inv(16)(p13.1q22) or t(16;16)(p13.1;q22) CBFB-MYH11", "Acute Myeloid Leukemia with inv(16)(p13.1q22) or t(16;16)(p13.1;q22); CBFB-MYH11", "Acute myeloid leukaemia with inv(16)(p13.1q22) or t(16;16)(p13.1;q22) CBFB-MYH11", "Acute myeloid leukemia with inv(16)(p13.1q22) or t(16;16)(p13.1;q22) CBFB-MYH11 (disorder)", "Acute myeloid leukemia with inv(16)(p13.1q22) or t(16;16)(p13.1;q22) CBFB-MYH11 (diagnosis)", "Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute myeloid leukemia with inv(16)(p13.1q22) or t(16;16)(p13.1;q22) CBFB-MYH11", "shortest_name_length": 34}
{"curie": "MONDO:0020846", "names": ["MRT64", "MENTAL RETARDATION, autosomal recessive 64", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 64", "intellectual disability, autosomal recessive 64", "autosomal recessive intellectual developmental disorder 64", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 64"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 64", "shortest_name_length": 5}
{"curie": "MONDO:0004829", "names": ["ovary metastasis", "Krukenburg tumor", "Krukenberg Tumor", "krukenburg tumor", "krukenberg tumor", "Krukenberg tumor", "Krukenburg tumour", "Krukenberg tumour", "tumor; Krukenberg", "Tumor, Krukenberg", "Krukenbergs Tumor", "Krukenberg; tumor", "ovarian metastasis", "Krukenberg’s tumor", "Ovarian Metastasis", "krukenberg's tumor", "metastasis ovaries", "Krukenberg's Tumor", "Ovarian metastases", "Ovarian metastasis", "Krukenberg neoplasm", "metastasis to ovary", "Metastases to Ovary", "Metastases to ovary", "Metastasis to ovary", "Krukenberg Neoplasm", "Metastasis to Ovary", "Tumor, Krukenberg's", "Krukenberg Carcinoma", "Krukenberg carcinoma", "Carcinoma, Krukenberg", "Secondary tumor to ovary", "Secondary tumour to ovary", "Secondary cancer of ovary", "Cancer metastatic to ovary", "Krukenberg tumor (disorder)", "Metastatic Signet-Ring Cell Carcinoma", "Metastatic Signet Ring Cell Carcinoma", "secondary malignant neoplasm of ovary", "Metastatic signet ring cell carcinoma", "Secondary malignant neoplasm of ovary", "Metastatic malignant neoplasm to ovary", "Metastatic malignant neoplasm of ovary", "Metastatic Malignant Tumor to the Ovary", "metastasis of malignant neoplasm to ovary", "Metastatic Malignant Neoplasm in the Ovary", "Metastatic Malignant Neoplasm to the Ovary", "secondary malignant neoplasm genital organs ovary", "secondary malignant neoplasm of ovary (diagnosis)", "Metastatic malignant neoplasm to ovary (disorder)", "signet ring cell adenocarcinoma metastatic to ovary", "metastatic carcinoma to the ovary (Krukenberg tumor)", "metastasis of malignant neoplasm to ovary (diagnosis)", "Metastatic signet ring cell carcinoma (morphologic abnormality)", "signet ring cell adenocarcinoma metastatic to ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Krukenberg carcinoma", "shortest_name_length": 16}
{"curie": "MONDO:0007049", "names": ["ACROLEUKOPATHY, SYMMETRIC", "Acroleukopathy, Symmetric", "acroleukopathy, symmetric"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acroleukopathy, symmetric", "shortest_name_length": 25}
{"curie": "UMLS:C4763958", "names": ["Road Injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Road Injury", "shortest_name_length": 11}
{"curie": "MONDO:0024524", "names": ["DUH1", "dyschromatosis universalis hereditaria 1", "DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 1", "Dyschromatosis Universalis Hereditaria 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyschromatosis universalis hereditaria 1", "shortest_name_length": 4}
{"curie": "UMLS:C0751823", "names": ["Sagittal Sinus Septic Phlebitis", "Septic Phlebitis, Sagittal Sinus", "Phlebitis, Sagittal Sinus, Septic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Septic Phlebitis, Sagittal Sinus", "shortest_name_length": 31}
{"curie": "MONDO:0016207", "names": ["Phacogenic uveitis", "Phacotoxic uveitis", "uveitis lens-induced", "Lens-induced uveitis", "lens-induced uveitis", "Phacoantigenic uveitis", "Lens-associated uveitis", "phacoanaphylactic uveitis", "Phacoanaphylactic uveitis", "lens-induced iridocyclitis", "Lens-induced endophthalmitis", "lens-induced endophthalmitis", "Phacoallergic endophthalmitis", "Phacoantigenic endophthalmitis", "Lens-induced uveitis (disorder)", "Lens-induced uveitis (diagnosis)", "Endophthalmitis phacoanaphylactica", "Phako-anaphylactic endophthalmitis", "endophthalmitis phacoanaphylactica"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phacoanaphylactic uveitis", "shortest_name_length": 18}
{"curie": "MONDO:0600029", "names": ["Spirometric restriction", "Restrictive Lung Disease", "disease lung restrictive", "LUNG DISEASE RESTRICTIVE", "Restrictive lung disease", "restrictive lung disease", "RESTRICTIVE LUNG DISEASE", "diseases lung restrictive", "LUNG, RESTRICTIVE DISEASE", "restrictive pulmonary disease", "Restrictive lung disease, NOS", "Restrictive ventilatory defect", "Restrictive respiratory disease", "Restrictive respiratory syndrome", "Restrictive lung disease (disorder)", "restrictive lung disease (diagnosis)", "Restrictive respiratory insufficiency", "Restrictive deficit on pulmonary function tests", "Restrictive deficit on pulmonary function testing", "Stiff lung or chest wall causing decreased lung volume"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "restrictive pulmonary disease", "shortest_name_length": 23}
{"curie": "MONDO:0007270", "names": ["RCM", "Rcm", "RCM1", "restrictive cardiomyopathy 1", "familial restrictive cardiomyopathy 1", "Cardiomyopathy, Familial Restrictive, 1", "CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1", "cardiomyopathy, familial restrictive, 1", "cardiomyopathy, familial restrictive, type 1", "TNNI3 familial isolated restrictive cardiomyopathy", "familial isolated restrictive cardiomyopathy caused by mutation in TNNI3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiomyopathy, familial restrictive, 1", "shortest_name_length": 3}
{"curie": "MONDO:0012625", "names": ["RP37", "retinitis pigmentosa 37", "Retinitis Pigmentosa 37", "RETINITIS PIGMENTOSA 37", "NR2E3 retinitis pigmentosa", "retinitis pigmentosa type 37", "RETINITIS PIGMENTOSA 37 (disorder)", "retinitis pigmentosa caused by mutation in NR2E3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 37", "shortest_name_length": 4}
{"curie": "MONDO:0002190", "names": ["vulvar syringoma", "Vulvar Syringoma", "mammalian vulva syringoma", "syringoma of mammalian vulva"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar syringoma", "shortest_name_length": 16}
{"curie": "MONDO:0012726", "names": ["HANAC", "Hanac", "HANAC syndrome", "Hanac Syndrome", "Hereditary angiopathy-nephropathy-aneurysms-muscle cramps syndrome", "hereditary angiopathy-nephropathy-aneurysms-muscle cramps syndrome", "ANGIOPATHY, HEREDITARY, WITH NEPHROPATHY, ANEURYSMS, AND MUSCLE CRAMPS", "angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps", "Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps", "HANAC - hereditary angiopathy with nephropathy, aneurysms, and muscle cramps", "Hereditary Angiopathy with Nephropathy, Aneurysm, and Muscle Cramps Syndrome", "hereditary angiopathy with nephropathy, aneurysms, and muscle cramps syndrome", "Hereditary Angiopathy with Nephropathy, Aneurysms, and Muscle Cramps Syndrome", "Hereditary angiopathy with nephropathy, aneurysms, and muscle cramps syndrome", "Autosomal dominant familial hematuria, retinal arteriolar tortuosity, contractures", "Autosomal Dominant Familial Hematuria, Retinal Arteriolar Tortuosity, Contractures", "Autosomal dominant familial haematuria, retinal arteriolar tortuosity, contractures", "Hereditary angiopathy with nephropathy, aneurysms, and muscle cramps syndrome (disorder)", "autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome", "Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0005341", "names": ["BCC", "bcc", "Basiloma", "basalioma", "Basalioma", "Rodent ulcer", "Rodent Ulcer", "rodent ulcer", "Ulcer;rodent", "Rodent Ulcers", "rodent ulcers", "Ulcer, Rodent", "Ulcers, Rodent", "Basal cell nevi", "Basal Cell Tumor", "Basal cell nevus", "basal cell tumor", "Basal cell tumor", "Basal cell cancer", "basal cancer cell", "Basal Cell Cancer", "Basal cell tumour", "basal cell cancer", "RU - Rodent ulcer", "Cell Cancer, Basal", "Cancer, Basal Cell", "Basal Cell Cancers", "Basal Cell Neoplasm", "Cancers, Basal Cell", "Basal cell neoplasm", "Cell Cancers, Basal", "Basal Cell Carcinoma", "Neoplasm, Basal Cell", "BASAL CELL NEOPLASMS", "basal cell carcinoma", "BASAL CELL CARCINOMA", "CARCINOMA BASAL CELL", "Basal cell carcinoma", "Basal Cell Neoplasms", "Cell Neoplasm, Basal", "Carcinoma basal cell", "Cell Neoplasms, Basal", "basal cell carcinomas", "Carcinoma, Basal Cell", "Neoplasms, Basal Cell", "Basal Cell Carcinomas", "Basal cell carcinomas", "basal cell epithelioma", "Basal Cell Epithelioma", "Carcinomas, Basal Cell", "Skin Basal Cell Cancer", "BASAL CELL EPITHELIOMA", "skin basal cell cancer", "basal cell skin cancer", "Basal cell skin cancer", "epithelioma basal cell", "SKIN CANCER BASAL CELL", "Basal cell epithelioma", "Epithelioma basal cell", "EPITHELIOMA, BASAL CELL", "Epithelioma, Basal Cell", "skin cancer, basal cell", "Basal Cell Epitheliomas", "Basal cell carcinoma NOS", "Epitheliomas, Basal Cell", "Basal Cell Skin Carcinoma", "Basal cell carcinoma, NOS", "basal cell skin carcinoma", "skin basal cell carcinoma", "Skin Basal Cell Carcinoma", "Cancer of skin, basal cell", "BCC - Basal cell carcinoma", "malignant basal cell tumor", "carcinoma, basal cell, skin", "basal cell carcinoma of skin", "Basal cell carcinoma of skin", "Basal Cell Carcinoma of Skin", "BASAL CELL CARCINOMA OF SKIN", "malignant Basal cell neoplasm", "cancer of the skin, basal cell", "Basal Cell Carcinoma of the Skin", "Basal cell neoplasm (morphology)", "basal cell carcinoma of the skin", "carcinoma of the skin, basal cell", "SKIN CANCER, BASAL CELL CARCINOMA", "Basal cell epithelioma (diagnosis)", "BCC - Basal cell carcinoma of skin", "Skin cancers - basal cell carcinoma", "Basal cell tumor of uncertain behavior", "Basal cell carcinoma of skin (disorder)", "Basal cell tumour of uncertain behaviour", "basal cell carcinoma of skin (diagnosis)", "Basal cell neoplasm (morphologic abnormality)", "Basal cell carcinoma (morphologic abnormality)", "malignant neoplasm carcinoma epithelioma basal cell", "Basal cell tumor, uncertain whether benign or malignant", "Basal cell tumour, uncertain whether benign or malignant", "Basal cell tumor of uncertain behavior (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin basal cell carcinoma", "shortest_name_length": 3}
{"curie": "MONDO:0011718", "names": ["CILD2", "primary ciliary dyskinesia 2", "Primary ciliary dyskinesia, 2", "CILIARY DYSKINESIA, PRIMARY, 2", "ciliary dyskinesia, primary, 2", "Ciliary Dyskinesia, Primary, 2", "DNAAF3 primary ciliary dyskinesia", "primary ciliary dyskinesia type 2", "ciliary dyskinesia, primary, type 2", "primary ciliary dyskinesia caused by mutation in DNAAF3", "primary ciliary dyskinesia 2 with or without situs inversus", "CILIARY DYSKINESIA, PRIMARY, 2, WITH OR WITHOUT SITUS INVERSUS", "ciliary dyskinesia, primary, 2, with or without situs inversus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia 2", "shortest_name_length": 5}
{"curie": "UMLS:C4055196", "names": ["Congenital isolated ACTH deficiency", "Congenital Isolated ACTH Deficiency", "Congenital Isolated Adrenocorticotropic Hormone Deficiency", "Congenital isolated adrenocorticotropic hormone deficiency", "Congenital isolated ACTH (adrenocorticotropic hormone) deficiency", "Congenital isolated adrenocorticotropic hormone deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital isolated adrenocorticotropic hormone deficiency", "shortest_name_length": 35}
{"curie": "MONDO:0019534", "names": ["mixed AIHA", "Mixed AIHA", "mixed-type autoimmune hemolytic anemia", "mixed type autoimmune hemolytic anemia", "Autoimmune hemolytic anemia mixed type", "Mixed type autoimmune hemolytic anemia", "Mixed-type autoimmune hemolytic anemia", "Mixed type autoimmune hemolytic disease", "Autoimmune haemolytic anaemia mixed type", "anemia hemolytic acquired autoimmune mixed type", "Autoimmune hemolytic anemia mixed type (disorder)", "mixed type autoimmune hemolytic anemia (diagnosis)", "Mixed type, cold and warm, (primary) (secondary) (symptomatic) autoimmune hemolytic anemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed-type autoimmune hemolytic anemia", "shortest_name_length": 10}
{"curie": "MONDO:0018715", "names": ["congenital angioma", "Congenital Angioma", "congenital hemangioma", "Hemangioma congenital", "HEMANGIOMA CONGENITAL", "Congenital hemangioma", "Congenital Hemangioma", "HAEMANGIOMA CONGENITAL", "Congenital haemangioma", "Haemangioma congenital", "congenital hemangiomas", "Congenital hemangioma (disorder)", "congenital hemangioma (diagnosis)", "Congenital Non-Progressive Hemangioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital hemangioma", "shortest_name_length": 18}
{"curie": "MONDO:0042960", "names": ["Aur syndrome", "Sackey Sakati Aur syndrome", "Sackey-Sakati-Aur syndrome", "Pancytopenia multiple congenital anomalies", "pancytopenia multiple congenital anomalies", "multiple dysmorphic features and pancytopenia", "Multiple dysmorphic features and pancytopenia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sackey-Sakati-Aur syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0018456", "names": ["PCJIA", "polyarticular JIA", "Polyarticular JIA", "JUVENILE POLYARTHRITIS", "polyarthritis juvenile", "Juvenile polyarthritis", "juvenile polyarthritis", "polyarthritis; juvenile", "juvenile; polyarthritis", "Juvenile polyarticular arthritis", "juvenile polyarticular arthritis", "polyarticular juvenile idiopathic arthritis", "Polyarticular Juvenile Idiopathic Arthritis", "Polyarticular juvenile idiopathic arthritis", "juvenile idiopathic arthritis, polyarticular", "PJIA Polyarticular Juvenile Idiopathic Arthritis", "Polyarticular-Course Juvenile Idiopathic Arthritis", "Polyarticular juvenile idiopathic arthritis (disorder)", "polyarticular juvenile idiopathic arthritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyarticular juvenile idiopathic arthritis", "shortest_name_length": 5}
{"curie": "MONDO:0012015", "names": ["NYS3", "congenital nystagmus 3", "autosomal dominant congenital nystagmus 3", "NYSTAGMUS 3, congenital, autosomal dominant", "nystagmus 3, congenital, autosomal dominant", "Nystagmus 3, congenital, autosomal dominant", "NYSTAGMUS 3, CONGENITAL, AUTOSOMAL DOMINANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nystagmus 3, congenital, autosomal dominant", "shortest_name_length": 4}
{"curie": "MONDO:0002549", "names": ["Hypoglossal Schwannoma", "hypoglossal schwannoma", "hypoglossal neurilemmoma", "Hypoglossal Neurilemmoma", "hypoglossal nerve schwannoma", "Hypoglossal Nerve Schwannoma", "hypoglossal nerve neurilemmoma", "Hypoglossal Nerve Neurilemmoma", "schwannoma of hypoglossal nerve", "Schwannoma of Hypoglossal Nerve", "twelfth cranial nerve schwannoma", "Twelfth Cranial Nerve Schwannoma", "Neurilemmoma of Hypoglossal Nerve", "neurilemmoma of hypoglossal nerve", "twelfth cranial nerve neurilemmoma", "Twelfth Cranial Nerve Neurilemmoma", "schwannoma of twelfth cranial nerve", "schwannoma of the hypoglossal nerve", "Schwannoma of the Hypoglossal Nerve", "Schwannoma of Twelfth Cranial Nerve", "Neurilemmoma of the Hypoglossal Nerve", "neurilemmoma of the hypoglossal nerve", "neurilemmoma of twelfth cranial nerve", "Neurilemmoma of Twelfth Cranial Nerve", "schwannoma of the twelfth cranial nerve", "Schwannoma of the Twelfth Cranial Nerve", "Neurilemmoma of the Twelfth Cranial Nerve", "neurilemmoma of the twelfth cranial nerve"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schwannoma of twelfth cranial nerve", "shortest_name_length": 22}
{"curie": "UMLS:C0752208", "names": ["pseudodystonia", "Pseudodystonia", "Pseudodystonias", "Psychogenic Dystonia", "psychogenic dystonia", "Psychogenic dystonia", "Dystonia, Psychogenic", "Psychogenic Dystonias", "Dystonias, Psychogenic", "Psychogenic movement disorder", "Psychogenic movement disorders", "Psychogenic movement disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pseudodystonia", "shortest_name_length": 14}
{"curie": "UMLS:C1266015", "names": ["Delta Cell Carcinoma", "Malignant Somatostatinoma", "malignant somatostatinoma", "Somatostatinoma, malignant", "Somatostatin cell tumor, malignant", "Somatostatin cell tumour, malignant", "malignant somatostatinoma (diagnosis)", "Somatostatinoma, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Somatostatinoma, malignant", "shortest_name_length": 20}
{"curie": "MONDO:0012296", "names": ["Lipomyelomeningocele", "lipomyelomeningocele", "LIPOMYELOMENINGOCELE", "familial lipomyelomeningocele", "Lipomyelomeningocele (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lipomyelomeningocele", "shortest_name_length": 20}
{"curie": "UMLS:C0796619", "names": ["Stage IIA Soft Tissue Sarcoma", "stage IIA soft tissue sarcoma", "Stage IIA Sarcoma of Soft Tissue", "Stage IIA Sarcoma of the Soft Tissue", "Stage IIA Soft Tissue Sarcoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Soft Tissue Sarcoma AJCC v7", "shortest_name_length": 29}
{"curie": "MONDO:0022912", "names": ["cutis verticis gyrata mental deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutis verticis gyrata mental deficiency", "shortest_name_length": 39}
{"curie": "OMIM:111000", "names": [], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"]}
{"curie": "MONDO:0020777", "names": ["CDGF2", "CONGENITAL DISORDER OF GLYCOSYLATION WITH DEFECTIVE FUCOSYLATION 2", "congenital disorder of glycosylation with defective fucosylation 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital disorder of glycosylation with defective fucosylation 2", "shortest_name_length": 5}
{"curie": "MONDO:0017194", "names": ["Blount", "tibia vara", "Tibia vara", "Tibia varum", "Blount Disease", "Blount disease", "Blount's Disease", "blount's disease", "Blount's disease", "tibia vara Blount", "Non-rachitic bowleg", "infantile tibia vara", "Blount-Barber syndrome", "Blount; osteochondrosis", "osteochondrosis; Blount", "Erlacher-Blount syndrome", "Osteochondrosis of Blount", "Osteochondrosis Deformans Tibiae", "Osteochondrosis deformans tibiae", "Juvenile osteochondrosis of proximal tibia", "juvenile osteochondrosis of proximal tibia", "Aseptic necrosis of medial condyle of tibia", "juvenile osteochondrosis of proximal tibia (diagnosis)", "familial infantile type osteochondrosis deformans tibiae", "Osteochondrosis deformans tibiae, familial infantile type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Blount disease", "shortest_name_length": 6}
{"curie": "UMLS:C0154129", "names": ["borderline neoplasm", "Borderline Neoplasm", "borderline malignancy tumor", "Tumor, borderline malignancy", "Tumour, borderline malignancy", "Neoplasm of uncertain behavior", "neoplasm of uncertain behavior", "Neoplasm of uncertain behaviour", "Neoplasms of uncertain behavior", "NEOPLASMS OF UNCERTAIN BEHAVIOR", "Neoplasms of uncertain behaviour", "Neoplasm of Borderline Malignancy", "neoplasm of borderline malignancy", "Neoplasm of Low Malignant Potential", "neoplasm of low malignant potential", "Neoplastic disease of uncertain behavior", "neoplasm of uncertain malignant potential", "Unclassified tumor, borderline malignancy", "Neoplastic disease of uncertain behaviour", "Neoplasm of Uncertain Malignant Potential", "neoplasm of uncertain behavior (diagnosis)", "Unclassified tumour, borderline malignancy", "Neoplasms of Uncertain and Unknown Behavior", "Tumor, uncertain whether benign or malignant", "Tumour, uncertain whether benign or malignant", "uncertain whether benign or malignant neoplasm", "Neoplasm, Uncertain Whether Benign or Malignant", "Neoplasm, uncertain whether benign or malignant", "Neoplastic disease of uncertain behavior (disorder)", "Neoplasm of uncertain behavior (morphologic abnormality)", "Unclassified tumor, uncertain whether benign or malignant", "Unclassified tumour, uncertain whether benign or malignant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplasm of uncertain behavior", "shortest_name_length": 19}
{"curie": "MONDO:0001334", "names": ["eyelid; hypertrichosis", "hypertrichosis; eyelid", "hypertrichosis of eyelid", "Hypertrichosis of eyelid", "eyelid disorder hypertrichosis", "eyelid hypertrichosis (disease)", "hypertrichosis (disease) of eyelid", "Hypertrichosis of eyelid (disorder)", "hypertrichosis of eyelid (diagnosis)", "hypertrichosis of eyelid (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrichosis of eyelid", "shortest_name_length": 22}
{"curie": "UMLS:C4526514", "names": ["Rectal Carcinoma Metastatic in the Liver"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rectal Carcinoma Metastatic in the Liver", "shortest_name_length": 40}
{"curie": "MONDO:0003852", "names": ["ovarian solid teratoma", "Ovarian Solid Teratoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian solid teratoma", "shortest_name_length": 22}
{"curie": "MONDO:0006984", "names": ["subdural abscess", "Subdural Empyema", "Subdural empyema", "Subdural Abscess", "Subdural abscess", "subdural empyema", "Subdural Empyemas", "subdural; empyema", "ABSCESS, SUBDURAL", "subdural; abscess", "Empyema, subdural", "Empyema, Subdural", "empyema; subdural", "abscess; subdural", "PACHYMENINGITIS, SUBDURAL", "Subdural abscess (disorder)", "subdural empyema (diagnosis)", "EMPYEMA, SUBDURAL, INTRACRANIAL", "Empyema (collection of pus), subdural space"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subdural empyema", "shortest_name_length": 16}
{"curie": "UMLS:C0238201", "names": ["IODISM", "Iodism", "iodism", "iodine toxicity", "IODINE POISONING", "iodine poisoning", "Iodine poisoning", "toxicity from iodine", "Iodine poisoning syndrome", "iodine toxicity (diagnosis)", "Iodine poisoning (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Iodine poisoning", "shortest_name_length": 6}
{"curie": "MONDO:0010282", "names": ["MTBSX", "mycobacterium tuberculosis, susceptibility, X-linked", "mycobacterium tuberculosis, susceptibility to, X-linked", "MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, X-LINKED", "MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, X-LINKED (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mycobacterium tuberculosis, susceptibility to, X-linked", "shortest_name_length": 5}
{"curie": "MONDO:0000469", "names": ["SA node", "sinuatrial node", "sinoatrial node disease", "sinoatrial node disorder", "disease of sinoatrial node", "disorder of sinoatrial node", "sinoatrial node disease or disorder", "disease or disorder of sinoatrial node"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sinoatrial node disorder", "shortest_name_length": 7}
{"curie": "UMLS:C0275706", "names": ["kansasii; Mycobacterium", "Mycobacterium; kansasii", "Mycobacterium kansasii infection", "MYCOBACTERIUM KANSASII INFECTION", "Infection due to Mycobacterium kansasii", "Infection caused by Mycobacterium kansasii", "Infection caused by Mycobacterium kansasii (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infection due to Mycobacterium kansasii", "shortest_name_length": 23}
{"curie": "MONDO:0016152", "names": ["qualitative or quantitative defects of calpain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of calpain", "shortest_name_length": 46}
{"curie": "MONDO:0010415", "names": ["RBMX1B", "reducing body myopathy 1B", "myopathy, reducing body, X-linked, childhood-onset", "Myopathy, Reducing Body, X-Linked, Childhood-Onset", "REDUCING BODY MYOPATHY, X-LINKED 1B, WITH LATE CHILDHOOD OR ADULT ONSET", "reducing body myopathy, X-linked 1B, with late childhood or adult onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy, reducing body, X-linked, childhood-onset", "shortest_name_length": 6}
{"curie": "UMLS:C4744757", "names": ["Thyroid Gland Cavernous Hemangioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Cavernous Hemangioma", "shortest_name_length": 34}
{"curie": "UMLS:C0857495", "names": ["nose sore", "Sore nose", "sore nose", "nose sores", "noses sore"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sore nose", "shortest_name_length": 9}
{"curie": "UMLS:C1096582", "names": ["Campylobacter jejuni infection", "Campylobacter Jejuni Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Campylobacter jejuni infection", "shortest_name_length": 30}
{"curie": "UMLS:C4526714", "names": ["Stage IA1 Lung Cancer", "Stage IA1 Lung Cancer AJCC v8", "stage IA1 lung cancer AJCC v8", "stage IA1 non-small cell lung cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA1 Lung Cancer AJCC v8", "shortest_name_length": 21}
{"curie": "UMLS:C4743979", "names": ["Primary Extremity Melanoma", "Primary Melanoma of the Extremity", "Cutaneous Melanoma of the Extremity", "Primary Cutaneous Melanoma of the Extremity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous Melanoma of the Extremity", "shortest_name_length": 26}
{"curie": "MONDO:0010649", "names": ["Mgcn", "MGC1", "megalocornea", "Isolated congenital megalocornea", "isolated congenital megalocornea", "congenital anterior megalophthalmia", "Congenital anterior megalophthalmia", "Isolated congenital megalocornea (disorder)", "megalocornea 1, X-linked, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated congenital megalocornea", "shortest_name_length": 4}
{"curie": "UMLS:C1142300", "names": ["colitis clostridium", "clostridium colitis", "Clostridium colitis", "Clostridium Colitis", "Clostridial enterocolitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clostridium colitis", "shortest_name_length": 19}
{"curie": "MONDO:0009048", "names": ["CURVED NAIL OF FOURTH TOE", "curved nail of fourth toe", "CLAW-LIKE FINGERS AND TOES", "claw-like fingers and toes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "curved nail of fourth toe", "shortest_name_length": 25}
{"curie": "UMLS:C5555511", "names": ["Locally Advanced Malignant Digestive System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Malignant Digestive System Neoplasm", "shortest_name_length": 52}
{"curie": "UMLS:C1333012", "names": ["Childhood Testicular Yolk Sac Tumor", "Pediatric Testicular Yolk Sac Tumor", "Pediatric Testicular Yolk Sac Neoplasm", "Childhood Testicular Yolk Sac Neoplasm", "Pediatric Testicular Endodermal Sinus Tumor", "Childhood Testicular Endodermal Sinus Tumor", "Childhood Testicular Endodermal Sinus Neoplasm", "Pediatric Testicular Endodermal Sinus Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Testicular Yolk Sac Tumor", "shortest_name_length": 35}
{"curie": "UMLS:C5205909", "names": ["Prostate Solitary Fibrous Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Solitary Fibrous Tumor", "shortest_name_length": 31}
{"curie": "UMLS:C0013609", "names": ["Local edema", "Local oedema", "local; edema", "edema; local", "Localized Edema", "Localized edema", "localized edema", "localized; edema", "Oedema;localised", "Localized oedema", "localised oedema", "edema; localized", "Localised oedema", "Edema, localized", "Localized edema NOS", "Localized edema (finding)", "Localized edema (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized Edema", "shortest_name_length": 11}
{"curie": "UMLS:C0854570", "names": ["Pocket Erosion", "Pocket erosion", "Erosion, pocket"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pocket erosion", "shortest_name_length": 14}
{"curie": "MONDO:0012116", "names": ["SCA8", "SPINOCEREBELLAR ATAXIA 8", "Spinocerebellar ataxia 8", "spinocerebellar ataxia 8", "Spinocerebellar ataxia type 8", "spinocerebellar ataxia type 8", "SCA8 Spinocerebellar ataxia 8", "Spinocerebellar ataxia type 8 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia type 8", "shortest_name_length": 4}
{"curie": "MONDO:0015385", "names": ["external auditory canal stenosis/atresia", "external auditory canal aplasia/hypoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "external auditory canal aplasia/hypoplasia", "shortest_name_length": 40}
{"curie": "MONDO:0009809", "names": ["MONA", "mona", "NAO SYNDROME", "NAO syndrome", "Torg Syndrome", "MONA spectrum", "TORG SYNDROME", "Torg syndrome", "Torg-Winchester syndrome", "Torg-Winchester Syndrome", "Torg osteolysis syndrome", "TORG-WINCHESTER SYNDROME", "Al-Aqeel Sewairi syndrome", "AL-AQEEL SEWAIRI SYNDROME", "Al-Aqeel Sewairi Syndrome", "Hereditary Multicentric Osteolysis", "Osteolysis hereditary multicentric", "Hereditary multicentric osteolysis", "Torg-Winchester syndrome, formerly", "TORG-WINCHESTER SYNDROME, FORMERLY", "OSTEOLYSIS, HEREDITARY MULTICENTRIC", "osteolysis, hereditary multicentric", "Osteolysis, Hereditary Multicentric", "Nodulosis-Arthropathy-Osteolysis Syndrome", "nodulosis-arthropathy-osteolysis syndrome", "NODULOSIS-ARTHROPATHY-OSTEOLYSIS SYNDROME", "Nodulosis-arthropathy-osteolysis syndrome", "MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY", "multicentric osteolysis, nodulosis, and arthropathy", "Multicentric Osteolysis, Nodulosis, and Arthropathy", "multicentric osteolysis nodulosis arthropathy spectrum", "Multicentric osteolysis-nodulosis-arthropathy spectrum", "Multicentric osteolysis nodulosis arthropathy spectrum", "MONA (multicentric osteolysis nodulosis arthropathy) spectrum", "Multicentric osteolysis nodulosis arthropathy spectrum (disorder)", "multicentric osteolysis nodulosis arthropathy spectrum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multicentric osteolysis, nodulosis, and arthropathy", "shortest_name_length": 4}
{"curie": "MONDO:0000066", "names": ["mitochondrial complex deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex deficiency", "shortest_name_length": 32}
{"curie": "MONDO:0014928", "names": ["JBTS28", "JOUBERT SYNDROME 28", "Joubert syndrome 28", "MKS1 Joubert syndrome", "Joubert syndrome type 28", "Joubert syndrome caused by mutation in MKS1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome 28", "shortest_name_length": 6}
{"curie": "UMLS:C1883177", "names": ["Stromal tumor with minor sex cord elements", "Stromal Tumor with Minor Sex Cord Elements", "Ovarian Stromal Tumor with Minor Sex Cord Elements"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Stromal Tumor with Minor Sex Cord Elements", "shortest_name_length": 42}
{"curie": "UMLS:C1706855", "names": ["Atrial Perforation", "Atrial perforation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atrial perforation", "shortest_name_length": 18}
{"curie": "UMLS:C1332052", "names": ["AIDS-Related Non-Hodgkin's Lymphoma of Cervix", "AIDS-Related Non-Hodgkin Lymphoma of the Cervix", "AIDS-Related Non-Hodgkin's Lymphoma of the Cervix", "AIDS-Related Uterine Cervical Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Non-Hodgkin Lymphoma of the Cervix", "shortest_name_length": 45}
{"curie": "MONDO:0024892", "names": ["Amyloid tumor", "amyloid tumor", "amyloid tumour", "Amyloid tumour", "Amyloid neoplasm", "amyloid neoplasm", "soft tissue amyloid tumor", "Soft Tissue Amyloid Tumor", "Soft Tissue Amyloid Neoplasm", "soft tissue amyloid neoplasm", "Amyloid tumor (morphologic abnormality)", "amyloid tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "soft tissue amyloid neoplasm", "shortest_name_length": 13}
{"curie": "MONDO:0005900", "names": ["Parotitis", "parotitis", "PAROTITIS", "parotiditis", "Parotiditis", "Parotitides", "Parotiditides", "Parotitis NOS", "Parotitis, NOS", "Parotitis (disorder)", "parotitis (diagnosis)", "parotid gland inflammation", "inflammation of parotid gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parotitis", "shortest_name_length": 9}
{"curie": "UMLS:C2984085", "names": ["Esophageal Cancer by AJCC v7 Stage", "Esophageal Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Cancer by AJCC v7 Stage", "shortest_name_length": 34}
{"curie": "MONDO:0011591", "names": ["CAAR", "CTRCT26", "cataract 26 multiple types", "cataract 26, multiple types", "CATARACT 26, MULTIPLE TYPES", "cataract, autosomal recessive, early-onset, pulverulent", "CATARACT, AUTOSOMAL RECESSIVE, EARLY-ONSET, PULVERULENT", "Cataract, Autosomal Recessive, Early-Onset, Pulverulent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 26 multiple types", "shortest_name_length": 4}
{"curie": "MONDO:0021289", "names": ["stage 0 cecum carcinoma", "Stage 0 Cecum Carcinoma", "cecum carcinoma in situ", "Cecum Carcinoma In Situ", "stage 0 caecum carcinoma", "caecum carcinoma in situ", "caecum in situ carcinoma", "Carcinoma In Situ of Cecum", "Carcinoma in situ of cecum", "carcinoma in situ of cecum", "carcinoma in situ of caecum", "Carcinoma in situ of caecum", "carcinoma in situ of the cecum", "Carcinoma In Situ of the Cecum", "Cecum Carcinoma In Situ AJCC v6", "cecum carcinoma in situ aJCC v6", "Cecum Carcinoma In Situ AJCC v7", "cecum carcinoma in situ aJCC v7", "Carcinoma in situ of cecum (disorder)", "carcinoma in situ of cecum (diagnosis)", "large intestine neoplasm carcinoma in situ cecum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma in situ of cecum", "shortest_name_length": 23}
{"curie": "MONDO:0014162", "names": ["COXPD16", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 16", "combined oxidative phosphorylation deficiency 16", "combined oxidative phosphorylation defect type 16", "MRPL44 combined oxidative phosphorylation deficiency", "combined oxidative phosphorylation deficiency type 16", "infantile hypertrophic cardiomyopathy due to MRPL44 deficiency", "combined oxidative phosphorylation deficiency caused by mutation in MRPL44"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile hypertrophic cardiomyopathy due to MRPL44 deficiency", "shortest_name_length": 7}
{"curie": "MONDO:0014954", "names": ["EDSPD2", "Ehlers-Danlos syndrome periodontal type 2", "Ehlers-Danlos syndrome, periodontal type 2", "Ehlers-Danlos syndrome, periodontal type, 2", "EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ehlers-Danlos syndrome, periodontal type 2", "shortest_name_length": 6}
{"curie": "UMLS:C0235351", "names": ["TONGUE ULCER", "Ulcer;tongue", "ulcer tongue", "tongue ulcer", "ulcer; tongue", "tongue; ulcer", "tongue ulcers", "Ulcer on tongue", "ulcer on tongue", "Tongue ulceration", "tongue ulceration", "ULCERATION TONGUE", "ulceration tongue", "TONGUE ULCERATION", "Ulceration tongue", "tongue ulcerations", "Ulceration of tongue", "Ulcer of tongue, NOS", "ulceration of tongue", "Tongue ulceration, NOS", "Ulcer on tongue (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ulcer on tongue", "shortest_name_length": 12}
{"curie": "UMLS:C1332293", "names": ["Castleman Disease, Hyaline-Vascular Type", "Castleman's Disease, Hyaline-Vascular Type", "Angiofollicular Lymphoid Hyperplasia, Hyaline-Vascular Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Castleman Disease, Hyaline-Vascular Type", "shortest_name_length": 40}
{"curie": "UMLS:C4727595", "names": ["Metastatic Ureter Carcinoma", "Metastatic Carcinoma of Ureter", "Metastatic Carcinoma of the Ureter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Ureter Carcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C4764239", "names": ["Locally Advanced Salivary Gland Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Salivary Gland Carcinoma", "shortest_name_length": 41}
{"curie": "UMLS:C0155170", "names": ["Conjunctiva Cyst", "Conjunctival Cyst", "Conjunctival cyst", "conjunctival cyst", "cyst; conjunctiva", "conjunctiva; cyst", "conjunctival cysts", "Conjunctival cysts", "cyst of conjunctiva", "Cyst of conjunctiva", "Cyst of Conjunctiva", "Cyst of the Conjunctiva", "conjunctival cyst (diagnosis)", "Cyst of conjunctiva (disorder)", "cyst of conjunctiva (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conjunctival cyst", "shortest_name_length": 16}
{"curie": "UMLS:C1511254", "names": ["Borderline Fallopian Tube Endometrioid Tumor", "Borderline Fallopian Tube Endometrioid Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Fallopian Tube Endometrioid Tumor", "shortest_name_length": 44}
{"curie": "MONDO:0032906", "names": ["SPG82", "hereditary spastic paraplegia 82", "spastic paraplegia 82 autosomal recessive", "spastic paraplegia 82, autosomal recessive", "SPASTIC PARAPLEGIA 82, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic paraplegia 82, autosomal recessive", "shortest_name_length": 5}
{"curie": "MONDO:0020560", "names": ["ATRT", "AT/RT", "ATT/RHT", "CNS rhabdoid tumor", "CNS Rhabdoid Tumor", "CNS Rhabdoid Neoplasm", "rhabdoid tumor of CNS", "CNS rhabdoid neoplasm", "Rhabdoid Tumor of CNS", "rhabdoid neoplasm of CNS", "Rhabdoid Neoplasm of CNS", "Rhabdoid tumor of the CNS", "rhabdoid tumor of the CNS", "Rhabdoid Tumor of the CNS", "Rhabdoid tumour of the CNS", "Rhabdoid Neoplasm of the CNS", "rhabdoid neoplasm of the CNS", "Malignant Brain Rhabdoid Tumor", "malignant brain rhabdoid tumor", "atypical teratoid rhabdoid tumor", "Atypical teratoid rhabdoid tumor", "atypical teratoid/rhabdoid tumor", "Atypical teratoid/rhabdoid tumor", "Atypical Teratoid Rhabdoid Tumor", "Atypical Teratoid/Rhabdoid Tumor", "atypical teratoid rhabdoid tumour", "Malignant Rhabdoid Tumor of Brain", "malignant brain rhabdoid neoplasm", "Atypical teratoid/rhabdoid tumour", "Malignant Brain Rhabdoid Neoplasm", "malignant rhabdoid tumor of brain", "Malignant Rhabdoid Neoplasm of Brain", "malignant rhabdoid neoplasm of brain", "Malignant Rhabdoid Tumor of the Brain", "Central Nervous System Rhabdoid Tumor", "central nervous system rhabdoid tumor", "malignant rhabdoid tumor of the brain", "primary malignant brain rhabdoid tumor", "rhabdoid tumor predisposition syndrome", "Primary Malignant Brain Rhabdoid Tumor", "rhabdoid tumor of central nervous system", "Malignant Rhabdoid Neoplasm of the Brain", "malignant rhabdoid neoplasm of the brain", "Rhabdoid Tumor of Central Nervous System", "Central Nervous System Rhabdoid Neoplasm", "central nervous system rhabdoid neoplasm", "primary malignant rhabdoid tumor of brain", "primary malignant brain rhabdoid neoplasm", "Primary Malignant Rhabdoid Tumor of Brain", "Primary Malignant Brain Rhabdoid Neoplasm", "rhabdoid neoplasm of central nervous system", "Rhabdoid Neoplasm of Central Nervous System", "Rhabdoid Tumor of the Central Nervous System", "Primary Malignant Rhabdoid Neoplasm of Brain", "rhabdoid tumor of the central nervous system", "primary malignant rhabdoid neoplasm of brain", "Primary Malignant Rhabdoid Tumor of the Brain", "primary malignant rhabdoid tumor of the brain", "Atypical Teratoid/Rhabdoid Tumor (WHO Grade 4)", "atypical teratoid/rhabdoid tumor (WHO grade IV)", "Rhabdoid Neoplasm of the Central Nervous System", "Atypical Teratoid/Rhabdoid Tumor (WHO Grade IV)", "rhabdoid neoplasm of the central nervous system", "primary malignant rhabdoid neoplasm of the brain", "Primary Malignant Rhabdoid Neoplasm of the Brain", "Atypical teratoid/rhabdoid tumor (morphologic abnormality)", "atypical teratoid/rhabdoid tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical teratoid rhabdoid tumor", "shortest_name_length": 4}
{"curie": "MONDO:0002806", "names": ["bronchus cancer", "Bronchi--Cancer", "cancer bronchus", "Bronchus Cancer", "bronchial cancer", "Cancer of bronchus", "bronchus carcinoma", "Carcinoma;bronchus", "BRONCHIAL CARCINOMA", "bronchial carcinoma", "Bronchial carcinoma", "Bronchial Carcinoma", "Bronchial Carcinomas", "Carcinoma, Bronchial", "carcinoma of bronchus", "Carcinomas, Bronchial", "Carcinoma of bronchus", "Bronchogenic Carcinoma", "Bronchogenic carcinoma", "bronchogenic carcinoma", "Carcinoma, Bronchogenic", "Bronchiogenic Carcinoma", "bronchiogenic carcinoma", "Carcinoma bronchiogenic", "CA - Cancer of bronchus", "CARCINOMA BRONCHIOGENIC", "Bronchogenic Carcinomas", "Primary bronchial cancer", "Carcinomas, Bronchogenic", "bronchogenic lung cancer", "Bronchogenic Lung Cancer", "carcinoma of the bronchus", "CA - Carcinoma of bronchus", "malignant neoplasm bronchus", "BC - bronchogenic carcinoma", "BC - Bronchogenic carcinoma", "bronchogenic lung carcinoma", "Bronchogenic Lung Carcinoma", "LUNG, CARCINOMA, BRONCHOGENIC", "carcinoma, bronchial, malignant", "CARCINOMA, BRONCHIAL, MALIGNANT", "bronchus carcinoma cell squamous", "bronchus carcinoma squamous cell", "Carcinoma of bronchus (diagnosis)", "LUNG CANCER BRONCHOGENIC CARCINOMA", "Squamous cell carcinoma of bronchus", "squamous cell carcinoma of bronchus", "LUNG CANCER, BRONCHOGENIC CARCINOMA", "malignant neoplasm of bronchus carcinoma", "BRONCHOGENIC CARCINOMA SQUAMOUS CELL TYPE", "SCC - Squamous cell carcinoma of bronchus", "Squamous cell carcinoma of bronchus (disorder)", "Squamous cell carcinoma of bronchus (diagnosis)", "lung neoplasm malignant squamous cell carcinoma of bronchus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bronchogenic carcinoma", "shortest_name_length": 15}
{"curie": "UMLS:C0006112", "names": ["Metabolic Brain Disease", "Metabolic Brain Disorder", "Metabolic brain syndrome", "Brain Metabolic Disorder", "Metabolic Encephalopathy", "Metabolic encephalopathy", "ENCEPHALOPATHY METABOLIC", "encephalopathy metabolic", "metabolic encephalopathy", "metabolic brain diseases", "Brain Disease, Metabolic", "Metabolic Brain Syndrome", "Metabolic Brain Diseases", "Brain Metabolic Disorders", "Metabolic Brain Syndromes", "metabolic disorders brain", "Metabolic Brain Disorders", "Metabolic Disorder, Brain", "Encephalopathy, Metabolic", "Brain Disorder, Metabolic", "Brain Syndrome, Metabolic", "Brain Diseases, Metabolic", "Metabolic Disorders, Brain", "Brain Disorders, Metabolic", "Metabolic Encephalopathies", "Encephalopathies, Metabolic", "Metabolic encephalopathy NOS", "Metabolic brain syndrome, NOS", "Metabolic encephalopathy (disorder)", "metabolic encephalopathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brain Diseases, Metabolic", "shortest_name_length": 23}
{"curie": "UMLS:C0156221", "names": ["Glomerulonephritis acute", "Glomerulonephritis;acute", "acute glomerulonephritis", "Acute Glomerulonephritis", "GLOMERULONEPHRITIS ACUTE", "Acute glomerulonephritis", "glomerulonephritis acute", "glomerulonephritis; acute", "acute; glomerulonephritis", "GLOMERULONEPHRITIS, ACUTE", "Acute glomerulonephritis, NOS", "AGN - Acute glomerulonephritis", "Acute glomerulonephritis syndrome", "Acute glomerulonephritis (disorder)", "acute glomerulonephritis (diagnosis)", "Glomerulonephritis NOS, specified as acute"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute glomerulonephritis", "shortest_name_length": 24}
{"curie": "UMLS:C5670124", "names": ["Advanced Hormone Receptor-Positive Breast Carcinoma", "Advanced Hormone Receptor Positive Breast Carcinoma", "Advanced Hormone Receptor Positive Breast Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Hormone Receptor-Positive Breast Carcinoma", "shortest_name_length": 51}
{"curie": "UMLS:C5421350", "names": ["Refractory Acute Myeloid Leukemia Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Acute Myeloid Leukemia Not Otherwise Specified", "shortest_name_length": 57}
{"curie": "MONDO:0000188", "names": ["GLUT1DS", "GLUT1 deficiency syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "GLUT1 deficiency syndrome", "shortest_name_length": 7}
{"curie": "MONDO:0011158", "names": ["ALPS", "ALPS1A", "ALPS1B", "ALPS-FAS", "ALPS-FASL", "Type 1a ALPS", "Type 1b ALPS", "Canale-Smith syndrome", "autoimmune lymphoproliferative syndrome", "autoimmune lymphoproliferative syndrome type 1", "Type 1b Autoimmune Lymphoproliferative Syndrome", "Type 1a Autoimmune Lymphoproliferative Syndrome", "Autoimmune Lymphoproliferative Syndrome, Type IA", "Autoimmune Lymphoproliferative Syndrome, Type IB", "autoimmune lymphoproliferative syndrome, type 1A", "autoimmune lymphoproliferative syndrome, type IB", "autoimmune lymphoproliferative syndrome, type 1B", "AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IB", "autoimmune lymphoproliferative syndrome, type IA", "AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IA", "Autoimmune Lymphoproliferative Syndrome-FAS variant", "Autoimmune Lymphoproliferative Syndrome-FASL variant", "autoimmune lymphoproliferative syndrome, type I, autosomal dominant", "Autoimmune Lymphoproliferative Syndrome, Type I, Autosomal Recessive", "AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE I, AUTOSOMAL RECESSIVE", "autoimmune lymphoproliferative syndrome, type I, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune lymphoproliferative syndrome type 1", "shortest_name_length": 4}
{"curie": "MONDO:0001419", "names": ["Trachea Epidermoid Carcinoma", "trachea epidermoid carcinoma", "Tracheal Epidermoid carcinoma", "Tracheal Epidermoid Carcinoma", "tracheal epidermoid carcinoma", "Epidermoid Carcinoma of Trachea", "epidermoid carcinoma of trachea", "trachea squamous cell carcinoma", "Trachea Squamous Cell Carcinoma", "Tracheal Squamous Cell Carcinoma", "tracheal squamous cell carcinoma", "Squamous cell carcinoma of trachea", "squamous cell carcinoma of trachea", "Squamous Cell Carcinoma of Trachea", "epidermoid carcinoma of the trachea", "Epidermoid Carcinoma of the Trachea", "squamous cell carcinoma of the trachea", "Squamous Cell Carcinoma of the Trachea", "Squamous cell carcinoma of trachea (disorder)", "squamous cell carcinoma of trachea (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trachea squamous cell carcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0016832", "names": ["Dup7q11.23D", "distal dup(7)(q11.23)", "distal trisomy 7q11.23", "distal 7q11.23 microduplication syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal 7q11.23 microduplication syndrome", "shortest_name_length": 11}
{"curie": "UMLS:C0161820", "names": ["Urinary Complication", "Urinary complication", "urinary complication", "urinary complications", "Urinary complications", "Urinary complication, NOS", "Urinary complication (disorder)", "urinary complication (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urinary complication", "shortest_name_length": 20}
{"curie": "MONDO:0019891", "names": ["Del(22)", "22 monosomy", "Monosomy 22", "Deletion 22", "monosomy 22", "deletion 22", "monosomy type 22", "Monosomy 22 syndrome", "Monosomy 22 syndrome (disorder)", "chromosome 22 monosomy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "monosomy 22", "shortest_name_length": 7}
{"curie": "MONDO:0013381", "names": ["HSN1D", "hereditary sensory neuropathy type 1D", "hereditary sensory neuropathy type ID", "neuropathy, hereditary sensory, type 1D", "neuropathy, hereditary sensory, type ID", "NEUROPATHY, HEREDITARY SENSORY, TYPE ID"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuropathy, hereditary sensory, type 1D", "shortest_name_length": 5}
{"curie": "MONDO:0018240", "names": ["TRPV4-related bone disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "TRPV4-related bone disorder", "shortest_name_length": 27}
{"curie": "MONDO:0017592", "names": ["staphylococcal toxemia", "Staphylococcal toxemia", "Staphylococcal toxaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "staphylococcal toxemia", "shortest_name_length": 22}
{"curie": "MONDO:0004782", "names": ["DI", "diabete insipidus", "diabetes insipidus", "Diabetes Insipidus", "DIABETES INSIPIDUS", "Diabetes insipidus", "diabetes; insipidus", "Diabetes insipidus, NOS", "DI - Diabetes insipidus", "Diabetes insipidus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diabetes insipidus", "shortest_name_length": 2}
{"curie": "UMLS:C1332297", "names": ["Angiosarcoma Associated with Lymphedema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Angiosarcoma Associated with Lymphedema", "shortest_name_length": 39}
{"curie": "MONDO:0009822", "names": ["Otoonychoperoneal syndrome", "Otoonychoperoneal Syndrome", "OTOONYCHOPERONEAL SYNDROME", "otoonychoperoneal syndrome", "oto-onycho-peroneal syndrome", "Oto-onycho-peroneal syndrome", "Oto-onycho-peroneal syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "otoonychoperoneal syndrome", "shortest_name_length": 26}
{"curie": "UMLS:C0264863", "names": ["ENDOCARDITIS SUBACUTE", "subacute endocarditis", "endocarditis subacute", "Subacute endocarditis", "Endocarditis;subacute", "subacute; endocarditis", "Subacute endocarditis NOS", "Subacute endocarditis, NOS", "subacute infective endocarditis", "Subacute endocarditis (disorder)", "Subacute endocarditis (diagnosis)", "Subacute endocarditis, infective NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subacute endocarditis", "shortest_name_length": 21}
{"curie": "MONDO:0006139", "names": ["cervical metaplasia", "Cervical Metaplasia", "CERVICAL METAPLASIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical metaplasia", "shortest_name_length": 19}
{"curie": "UMLS:C1335121", "names": ["Oral Cavity Monomorphic Adenoma", "Monomorphic Adenoma of Oral Cavity", "Monomorphic Adenoma of the Oral Cavity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral Cavity Monomorphic Adenoma", "shortest_name_length": 31}
{"curie": "MONDO:0016697", "names": ["low grade ependymoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "low grade ependymoma", "shortest_name_length": 20}
{"curie": "MONDO:0004628", "names": ["Gastroduodenitis", "gastroduodenitis", "Gastritis and duodenitis", "gastritis and duodenitis", "Other specified gastritis", "Gastroduodenitis (disorder)", "gastroduodenitis (diagnosis)", "peptic ulcer gastroduodenitis", "Gastroduodenitis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastroduodenitis", "shortest_name_length": 16}
{"curie": "MONDO:0009280", "names": ["MSG poisoning", "E621 intolerance", "SIN-CIB-SYN SYNDROME", "POST-SINO-CIBAL SYNDROME", "chinese restaurant syndrome", "Chinese restaurant syndrome", "Chinese Restaurant Syndrome", "CHINESE RESTAURANT SYNDROME", "monosodium glutamate reaction", "MONOSODIUM GLUTAMATE REACTION", "Monosodium glutamate poisoning", "Monosodium glutamate intolerance", "Glutamate Monosodium Sensitivity", "monosodium glutamate sensitivity", "Reaction to monosodium glutamate", "MONOSODIUM GLUTAMATE SENSITIVITY", "poisoning by monosodium glutamate", "Intolerance to monosodium glutamate", "MSG - Monosodium glutamate intolerance", "MSG (monosodium glutamate) intolerance", "poisoning by monosodium glutamate (MSG)", "Sodium hydrogen L-glutamate intolerance", "MSG poisoning (Chinese restaurant syndrome)", "poisoning by monosodium glutamate (diagnosis)", "Intolerance to monosodium glutamate (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "monosodium glutamate sensitivity", "shortest_name_length": 13}
{"curie": "MONDO:0032634", "names": ["MC1DN31", "nuclear type mitochondrial complex I deficiency 31", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 31", "mitochondrial complex 1 deficiency, nuclear type 31"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 31", "shortest_name_length": 7}
{"curie": "MONDO:0009471", "names": ["intrinsic factor and r binder, combined congenital deficiency of", "INTRINSIC FACTOR AND R BINDER, COMBINED CONGENITAL DEFICIENCY OF", "Intrinsic Factor and R Binder, Combined Congenital Deficiency of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intrinsic factor and r binder, combined congenital deficiency of", "shortest_name_length": 64}
{"curie": "MONDO:0016242", "names": ["Hb-C disease", "Hb C disease", "Hb C-disease", "Homozygous for Hb C", "Hemoglobin C disease", "HEMOGLOBIN C DISEASE", "hemoglobin C disease", "Hemoglobin C Disease", "Hemoglobin-C Disease", "Hemoglobin-C Diseases", "Haemoglobin C disease", "C Disease, Hemoglobin", "Hemoglobin C Diseases", "Hemoglobin C-C disease", "C Diseases, Hemoglobin", "Haemoglobin C-C disease", "homozygous hemoglobin C disease", "hereditary hemoglobin C disease", "Hemoglobin C disease (disorder)", "homozygous hemoglobin C disease (diagnosis)", "hereditary hemoglobin C disease (diagnosis)", "disease (or disorder); hemoglobin or Hb, C (Hb-C)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemoglobin C disease", "shortest_name_length": 12}
{"curie": "MONDO:0009283", "names": ["GA3", "Ga 3", "GA III", "glutaric aciduria 3", "Glutaric Aciduria III", "glutaric aciduria III", "GLUTARIC ACIDURIA III", "Glutaric aciduria type 3", "Glutaric acidemia type 3", "glutaric acidemia type 3", "glutaric aciduria type 3", "glutaric acidemia type III", "glutaric aciduria type III", "Glutaryl-CoA oxidase deficiency", "glutaryl-Coa oxidase deficiency", "glutaryl-CoA oxidase deficiency", "GLUTARYL-CoA OXIDASE DEFICIENCY", "Glutaryl-CoA Oxidase Deficiency", "SUGCT glutaric aciduria (disease)", "Glutaryl-coenzyme A oxidase deficiency", "Glutaryl-coenzyme A oxidase deficiency (disorder)", "glutaric aciduria (disease) caused by mutation in SUGCT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glutaric acidemia type 3", "shortest_name_length": 3}
{"curie": "MONDO:0019103", "names": ["bes", "benign exophthalmos syndrome", "Benign exophthalmos syndrome", "Benign exophthalmos syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign exophthalmos syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C3831528", "names": ["Antepartum Obstetric Air Embolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Antepartum Obstetric Air Embolism", "shortest_name_length": 33}
{"curie": "MONDO:0002112", "names": ["Mesothelioma of Peritoneum", "mesothelioma of peritoneum", "Peritoneal Adenomatoid Tumor", "peritoneal adenomatoid tumor", "peritoneum benign mesothelioma", "Benign Peritoneal Mesothelioma", "benign peritoneal mesothelioma", "peritoneum; benign mesothelioma", "mesothelioma; benign, peritoneum", "peritoneum; mesothelioma, benign", "Benign mesothelioma of peritoneum", "benign peritoneal neoplasm - mesothelial tissue", "Benign neoplasm of mesothelial tissue of peritoneum", "benign neoplasm of mesothelial tissue of peritoneum", "Benign neoplasm of mesothelial tissue of peritoneum (disorder)", "benign neoplasm of mesothelial tissue of peritoneum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign peritoneal mesothelioma", "shortest_name_length": 26}
{"curie": "MONDO:0005898", "names": ["PARONYCHIA", "Paronychia", "paronychia", "Perionychia", "perionychia", "Paronychias", "Paronychitis", "infected nailfold", "Infected nailfold", "paronychia (disease)", "fungal nail infection", "Paronychia (disorder)", "Nail bed inflammation", "paronychia (diagnosis)", "paronychia inflammation", "Paronychia Inflammation", "onychia and paronychia of toe", "Onychia and paronychia of toe", "onychia and paronychia of finger", "Onychia and paronychia of finger"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paronychia", "shortest_name_length": 10}
{"curie": "UMLS:C3509286", "names": ["Alcoholic Cirrhosis with Ascites", "Alcoholic Liver Cirrhosis with Ascites", "Alcoholic cirrhosis of liver with ascites", "alcoholic (Laennec's) cirrhosis with ascites", "alcoholic (Laennec's) cirrhosis with ascites (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alcoholic (Laennec's) cirrhosis with ascites", "shortest_name_length": 32}
{"curie": "MONDO:0009358", "names": ["COND", "cond", "cerebroosteonephosis syndrome", "CEREBROOSTEONEPHOSIS SYNDROME", "Cerebroosteonephrosis syndrome", "HUTTERITE CEREBROOSTEONEPHRODYSPLASIA SYNDROME", "Hutterite cerebroosteonephrodysplasia syndrome", "Congenital shortness with mild spondylorhizomelic dwarfism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hutterite cerebroosteonephrodysplasia syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C2350878", "names": ["Focal Emphysema", "Focal Emphysemas", "Emphysema, Focal", "Emphysemas, Focal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Focal Emphysema", "shortest_name_length": 15}
{"curie": "UMLS:C4528627", "names": ["Primary cutaneous CD4-positive small/medium T-cell lymphoma", "Primary cutaneous CD4-positive small/medium T-cell lymphoproliferative disorder", "Primary Cutaneous CD4-Positive Small/Medium T-Cell Lymphoproliferative Disorder", "Primary cutaneous CD4 positive small/medium T-cell lymphoproliferative disorder", "Primary Cutaneous CD4-Positive Small/Medium-Sized T-Cell Lymphoproliferative Disorder", "Primary Cutaneous CD4-Positive Small/Medium-Sized  T-Cell Lymphoproliferative Disorder", "PCSM-TCL- primary cutaneous CD4 positive small/medium T-cell lymphoproliferative disorder", "Primary cutaneous CD4 positive small/medium T-cell lymphoproliferative disorder (disorder)", "Primary Cutaneous CD4-Positive Small/Medium-Sized Pleomorphic T-Cell Lymphoproliferative Disorder", "Primary cutaneous CD4-positive small/medium T-cell lymphoproliferative disorder (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary cutaneous CD4 positive small/medium T-cell lymphoproliferative disorder", "shortest_name_length": 59}
{"curie": "UMLS:C2698045", "names": ["MCV Infection", "MCPyV Infection", "Merkel cell polyomavirus infection", "Merkel Cell Polyomavirus Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Merkel cell polyomavirus infection", "shortest_name_length": 13}
{"curie": "MONDO:0010543", "names": ["MGA2", "BTHS", "MGCA2", "MGA Type 2", "TAZ defect", "MGA type 2", "Mga, type 2", "Type 2, MGA", "MGA Type 2s", "MGA type II", "MGA Type II", "MGA, TYPE II", "MGA Type IIs", "Type II, MGA", "Type 2s, MGA", "Type IIs, MGA", "BARTH syndrome", "BARTH SYNDROME", "Barth syndrome", "barth syndrome", "Barth Syndrome", "Syndrome, Barth", "barths syndrome", "Barth syndrome (diagnosis)", "3-methylglutaconicaciduria type 2", "3-Methylglutaconicaciduria Type 2", "3-Methylglutaconicaciduria type 2", "3 Methylglutaconicaciduria Type 2", "3-Methylglutaconicaciduria type II", "3-Methylglutaconic Aciduria Type 2", "3-methylglutaconicaciduria type II", "3-Methylglutaconicaciduria Type II", "3-methylglutaconic aciduria type 2", "Barth syndrome, X-linked recessive", "Type 2, 3-Methylglutaconicaciduria", "3-Methylglutaconicaciduria Type 2s", "3-Methylglutaconic aciduria type 2", "3-methylglutaconic aciduria type II", "3-Methylglutaconicaciduria Type IIs", "3-Methylglutaconic aciduria, type 2", "3-METHYLGLUTACONIC ACIDURIA, TYPE II", "3-Methylglutaconic Aciduria, Type II", "3 Methylglutaconic Aciduria, Type II", "cardioskeletal myopathy-neutropenia syndrome", "Cardioskeletal myopathy-neutropenia syndrome", "3-Methylglutaconic aciduria type 2 (disorder)", "X-linked cardioskeletal myopathy and neutropenia", "Cardioskeletal myopathy with neutropenia and abnormal mitochondria", "cardioskeletal myopathy with neutropenia and abnormal mitochondria", "CARDIOSKELETAL MYOPATHY WITH NEUTROPENIA AND ABNORMAL MITOCHONDRIA", "Cardioskeletal Myopathy with Neutropenia and Abnormal Mitochondria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Barth syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C5447325", "names": ["PIRD", "Primary Immune Regulatory Disorder", "Primary Immune Dysregulation Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Immune Regulatory Disorder", "shortest_name_length": 4}
{"curie": "MONDO:0018321", "names": ["Atypical juvenile Parkinsonism", "Atypical juvenile parkinsonism", "atypical juvenile parkinsonism", "Atypical juvenile parkinsonism (disorder)", "Atypical juvenile Parkinsonism (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical juvenile parkinsonism", "shortest_name_length": 30}
{"curie": "MONDO:0017363", "names": ["Carrington syndrome", "Carrington's disease", "Carrington's Disease", "chronic eosinophilic pneumonia", "Chronic eosinophilic pneumonia", "Carrington's pulmonary eosinophilia", "chronic eosinophilic pneumonia (CEP)", "Chronic eosinophilic pneumonia (CEP)", "idiopathic chronic eosinophilic pneumonia", "Chronic idiopathic eosinophilic pneumonia", "pneumonia eosinophilic idiopathic chronic", "chronic idiopathic eosinophilic pneumonia", "Idiopathic chronic eosinophilic pneumonia", "eosinophilic idiopathic chronic pneumopathy", "Eosinophilic idiopathic chronic pneumopathy", "Idiopathic chronic eosinophilic pneumonia (disorder)", "Idiopathic chronic eosinophilic pneumonia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic chronic eosinophilic pneumonia", "shortest_name_length": 19}
{"curie": "MONDO:0003383", "names": ["Fallopian Tube Clear Cell Carcinoma", "fallopian tube clear cell carcinoma", "clear cell carcinoma of fallopian tube", "Clear Cell Carcinoma of Fallopian Tube", "Fallopian Tube Clear Cell Adenocarcinoma", "fallopian tube clear cell adenocarcinoma", "Clear Cell Carcinoma of the Fallopian Tube", "clear cell carcinoma of the fallopian tube", "Clear cell carcinoma of the fallopian tube", "Clear Cell Adenocarcinoma of Fallopian Tube", "clear cell adenocarcinoma of fallopian tube", "clear cell adenocarcinoma of the fallopian tube", "Clear Cell Adenocarcinoma of the Fallopian Tube", "clear cell adenocarcinoma of fallopian tube (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fallopian tube clear cell adenocarcinoma", "shortest_name_length": 35}
{"curie": "MONDO:0016494", "names": ["regional variant of GBS", "regional variant of Guillain-Barre syndrome", "regional variant of Guillain-Barré syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "regional variant of Guillain-Barre syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0010487", "names": ["MRX99", "XLID99", "X-linked mental retardation 99", "mental retardation, X-linked 99", "MENTAL RETARDATION, X-LINKED 99", "mental retardation, X-linked type 99", "intellectual disability, X-linked 99", "intellectual disability, X-linked type 99", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 99", "non-syndromic X-linked intellectual disability 99", "USP9X non-syndromic X-linked intellectual disability", "intellectual developmental disorder, X-linked 99, X-linked recessive", "non-syndromic X-linked intellectual disability caused by mutation in USP9X"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 99", "shortest_name_length": 5}
{"curie": "MONDO:0032919", "names": ["MRD62", "intellectual developmental disorder 62", "INTELLECTUAL DEVELOPMENTAL DISORDER 62", "Mental Retardation, Autosomal Dominant 62", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 62", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 62"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder 62", "shortest_name_length": 5}
{"curie": "UMLS:C0861832", "names": ["Recurrent Duodenal Cancer", "Duodenal carcinoma recurrent", "Recurrent Duodenal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Duodenal carcinoma recurrent", "shortest_name_length": 25}
{"curie": "MONDO:0014741", "names": ["DESSH", "DESANTO-SHINAWI SYNDROME", "Desanto-Shinawi syndrome", "DESANTO-SHINAWI syndrome", "chromosome 10P12-p11 deletion syndrome", "CHROMOSOME 10p12-p11 DELETION SYNDROME", "DeSanto-Shinawi syndrome due to WAC point mutation", "developmental delay, behavioral abnormalities, Facial Dysmorphism, and ocular abnormalities", "DEVELOPMENTAL DELAY, BEHAVIORAL ABNORMALITIES, FACIAL DYSMORPHISM, AND OCULAR ABNORMALITIES", "facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DeSanto-Shinawi syndrome due to WAC point mutation", "shortest_name_length": 5}
{"curie": "UMLS:C0151821", "names": ["ACCIDENTAL OVERDOSE", "OVERDOSE ACCIDENTAL", "Overdose accidental", "Accidental overdose", "Accidental overdose (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Accidental overdose", "shortest_name_length": 19}
{"curie": "MONDO:0020599", "names": ["Acquired clotting factor deficiency", "acquired coagulation protein disease", "Acquired coagulation factor deficiency", "Acquired Coagulation Factor Deficiency", "acquired coagulation factor deficiency", "Acquired coagulation factor deficiency, NOS", "Acquired coagulation factor deficiency (disorder)", "acquired coagulation factor deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired coagulation factor deficiency", "shortest_name_length": 35}
{"curie": "UMLS:C5419168", "names": ["COVID-19-Associated Ataxia", "SARS-CoV-2-Associated Ataxia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "COVID-19-Associated Ataxia", "shortest_name_length": 26}
{"curie": "UMLS:C0948167", "names": ["Factor IX inhibition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Factor IX inhibition", "shortest_name_length": 20}
{"curie": "MONDO:0100223", "names": ["MC1DN", "nuclear type mitochondrial complex I deficiency", "mitochondrial complex I deficiency, nuclear type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex I deficiency, nuclear type", "shortest_name_length": 5}
{"curie": "MONDO:0004106", "names": ["macrocystic pattern testicular yolk sac tumor", "Testicular Yolk Sac Tumor, Macrocystic Pattern", "testicular yolk sac tumor, macrocystic pattern"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular yolk sac tumor, macrocystic pattern", "shortest_name_length": 45}
{"curie": "UMLS:C1334185", "names": ["Infrequent Tumor", "Infrequent Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infrequent Neoplasm", "shortest_name_length": 16}
{"curie": "MONDO:0006638", "names": ["Acute retinal necrosis", "Acute Retinal Necrosis", "Acute Retinal Necroses", "RETINAL NECROSIS ACUTE", "acute retinal necrosis", "Retinal Necroses, Acute", "Necroses, Acute Retinal", "Retinal Necrosis, Acute", "Necrosis, Acute Retinal", "ARN - Acute retinal necrosis", "acute retinal necrosis syndrome", "Retinal Necrosis Syndrome, Acute", "Acute retinal necrosis (disorder)", "acute retinal necrosis (diagnosis)", "BARN - Bilateral acute retinal necrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute retinal necrosis syndrome", "shortest_name_length": 22}
{"curie": "UMLS:C1850599", "names": ["Leigh Syndrome due to Mitochondrial Complex IV Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leigh Syndrome due to Mitochondrial Complex IV Deficiency", "shortest_name_length": 57}
{"curie": "UMLS:C1699207", "names": ["anastomotic leak urethra", "Urethral anastomotic leak", "Urethral Anastomotic Leakage", "Urethral anastomotic leak (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urethral Anastomotic Leakage", "shortest_name_length": 24}
{"curie": "UMLS:C5205123", "names": ["Unresectable NUT Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable NUT Carcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0004574", "names": ["pyridoxine Deficincy", "Pyridoxine Deficincy", "ANEMIA B6 DEFICIENCY", "Pyridoxal deficiency", "Anemia B6 deficiency", "Anaemia B6 deficiency", "vitamin b6 deficiency", "b6 deficiency vitamin", "PYRIDOXINE DEFICIENCY", "B6 vitamin deficiency", "pyridoxine deficiency", "vitamin B6 deficiency", "B6 Vitamin Deficiency", "VITAMIN B6 DEFICIENCY", "Pyridoxine deficiency", "Pyridoxine Deficiency", "Vitamin B6 deficiency", "Vitamin B6 Deficiency", "VITAMIN DEFICIENCY B6", "deficiency, pyridoxine", "B6 deficiency, vitamin", "deficiency, B6 vitamin", "vitamin deficiency, B6", "deficiency, vitamin B6", "Deficiency, Pyridoxine", "Deficiency, Vitamin B6", "Vitamin B 6 Deficiency", "B6 Deficiency, Vitamin", "deficiency; pyridoxine", "Deficiency, B6 Vitamin", "Vitamin Deficiency, B6", "pyridoxine; deficiency", "Deficiency, Vitamin B 6", "Vitamin B6 Deficiencies", "deficiency; vitamin, B6", "vitamin B6 deficiencies", "Pyridoxamine deficiency", "vitamin; deficiency, B6", "B6 Vitamin Deficiencies", "B6 vitamin deficiencies", "deficiency, vitamin B 6", "B6 Deficiencies, Vitamin", "vitamin deficiencies, B6", "Vitamin Deficiencies, B6", "pyridoxamine; deficiency", "Deficiencies, Vitamin B6", "deficiencies, B6 vitamin", "Deficiencies, B6 Vitamin", "deficiency; pyridoxamine", "B6 deficiencies, vitamin", "deficiencies, vitamin B6", "Reduced vitamin b6 levels", "PYRIDOXINE DEFICIENCY ANEMIA", "ANEMIA PYRIDOXINE DEFICIENCY", "Anemia vitamin B6 deficiency", "Pyridoxine deficiency anemia", "pyridoxine deficiency anemia", "Anemia pyridoxine deficiency", "Pyridoxine deficiency anaemia", "Vitamin B6 deficiency disease", "Anaemia vitamin B6 deficiency", "Anaemia pyridoxine deficiency", "b6 deficiency diseases vitamin", "vitamin B6 deficiency syndrome", "Vitamin B6 deficiency syndrome", "syndrome; vitamin B6 deficiency", "vitamin B6; deficiency syndrome", "Vitamin B6 deficiency (disorder)", "pyridoxine deficiency (diagnosis)", "pyridoxine (vitamin B6) deficiency", "Anemia due to vitamin B6 deficiency", "Reduced circulating vitamin B6 level", "Anaemia due to vitamin B6 deficiency", "Anemia due to vitamin B>6< deficiency", "Anaemia due to vitamin B>6< deficiency", "Anemia due to vitamin B<sub>6</sub> deficiency", "Anemia due to vitamin B6 deficiency (disorder)", "Anaemia due to vitamin B<sub>6</sub> deficiency", "Anemia due to vitamin B>6< deficiency (disorder)", "Anemia due to vitamin B<sub>6</sub> deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyridoxine deficiency anemia", "shortest_name_length": 20}
{"curie": "UMLS:C4553668", "names": ["Stage IIIB Penile Cancer", "Stage IIIB Penile Cancer AJCC v8", "Stage IIIB Penile Squamous Cell Carcinoma AJCC v8", "Stage IIIB Squamous Cell Carcinoma of the Penis AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Penile Cancer AJCC v8", "shortest_name_length": 24}
{"curie": "MONDO:0017992", "names": ["autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis", "shortest_name_length": 79}
{"curie": "MONDO:0010000", "names": ["RCDFRD", "Rod-Cone Dystrophy, Sensorineural Deafness, and Fanconi-Type Renal Dysfunction", "ROD-CONE DYSTROPHY, SENSORINEURAL DEAFNESS, AND FANCONI-TYPE RENAL DYSFUNCTION", "rod-cone dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rod-cone dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction", "shortest_name_length": 6}
{"curie": "MONDO:0002598", "names": ["germinoma", "Germinoma", "germinomas", "Germinomas", "germinoma (disease)", "germinoma (diagnosis)", "Germinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "germinoma", "shortest_name_length": 9}
{"curie": "MONDO:0017830", "names": ["severe Canavan disease", "neonatal Canavan disease", "infantile Canavan disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe Canavan disease", "shortest_name_length": 22}
{"curie": "MONDO:0012019", "names": ["SEDK", "Sedk", "spondyloepiphyseal dysplasia Kimberley type", "Spondyloepiphyseal dysplasia Kimberley type", "spondyloepiphyseal dysplasia, Kimberley type", "SPONDYLOEPIPHYSEAL DYSPLASIA, KIMBERLEY TYPE", "Spondyloepiphyseal dysplasia, Kimberley type", "Spondyloepiphyseal Dysplasia, Kimberley Type", "Spondyloepiphyseal dysplasia Kimberley type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepiphyseal dysplasia, Kimberley type", "shortest_name_length": 4}
{"curie": "UMLS:C1386135", "names": ["depression acute", "Acute depression", "depression; acute", "acute; depression", "Acute depression (disorder)", "Acute depression (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute depression", "shortest_name_length": 16}
{"curie": "UMLS:C5205969", "names": ["Seminal Vesicle Angiosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Seminal Vesicle Angiosarcoma", "shortest_name_length": 28}
{"curie": "MONDO:0019390", "names": ["RED-M", "Susac syndrome", "Susac Syndrome", "Susacs Syndrome", "SICRET syndrome", "Syndrome, Susac", "Susac's syndrome", "Susac's Syndrome", "Syndrome, Susac's", "Retinocochleocerebral Vasculopathy", "Retinocochleocerebral vasculopathy", "Vasculopathy, Retinocochleocerebral", "Retinocochleocerebral Vasculopathies", "Vasculopathies, Retinocochleocerebral", "Retinocochleocerebral vasculopathy (disorder)", "small infarctions of cochlear, retinal and encephalic tissue", "retinopathy-encephalopathy-deafness associated with microangiopathy", "SICRET (small infarction of cochlear, retinal, and encephalic tissue) syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Susac syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0012131", "names": ["MNS", "MNS SYNDROME", "ENDOCHONDRAL GIGANTISM", "NISHIMURA-SCHMIDT SYNDROME", "MORENO-NISHIMURA-SCHMIDT SYNDROME", "Metaphyseal undermodeling, spondylar dysplasia, and overgrowth", "METAPHYSEAL UNDERMODELING, SPONDYLAR DYSPLASIA, AND OVERGROWTH", "metaphyseal undermodeling, spondylar dysplasia, and overgrowth", "overgrowth-metaphyseal undermodeling-spondylar dysplasia syndrome", "Overgrowth-metaphyseal undermodeling-spondylar dysplasia syndrome", "Overgrowth, metaphyseal undermodeling, spondylar dysplasia syndrome", "Overgrowth, metaphyseal undermodelling, spondylar dysplasia syndrome", "Overgrowth, metaphyseal undermodeling, spondylar dysplasia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metaphyseal undermodeling, spondylar dysplasia, and overgrowth", "shortest_name_length": 3}
{"curie": "MONDO:0800175", "names": ["shock heart", "heart shock", "heart shocking", "Cardiogenic shock", "Shock cardiogenic", "CARDIOGENIC SHOCK", "Cardiogenic Shock", "cardiogenic shock", "shock cardiogenic", "SHOCK CARDIOGENIC", "Shock, Cardiogenic", "Shock, cardiogenic", "cardiogenic; shock", "shock; cardiogenic", "Cardiovascular shock", "Cardiac shock syndrome", "Power failure syndrome", "cardiocirculatory collapse", "Cardiogenic shock (disorder)", "cardiogenic shock (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiogenic shock", "shortest_name_length": 11}
{"curie": "UMLS:C2981237", "names": ["Stage IV Rectosigmoid Cancer", "Stage IV Rectosigmoid Cancer AJCC v6", "Stage IV Rectosigmoid Carcinoma AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Rectosigmoid Cancer AJCC v6", "shortest_name_length": 28}
{"curie": "MONDO:0019754", "names": ["MCD", "PMCD", "multicentric Castleman disease", "Multicentric Castleman Disease", "Multicentric Castleman disease", "Castleman disease, multicentric", "Multicentric Castleman's Disease", "Multicentric Castleman's disease", "multicentric Castleman's disease", "Multi-centric Castleman's Disease", "multicentric giant lymph node hyperplasia", "Multicentric Castleman disease (disorder)", "idiopathic multicentric Castleman's disease", "Plasmablastic multicentric Castleman disease", "plasmablastic multicentric Castleman disease", "HHV-8-associated multicentric Castleman disease", "multicentric angiofollicular lymphoid hyperplasia", "multicentric Angiofollicular lymphoid hyperplasia", "Multicentric Angiofollicular Lymphoid Hyperplasia", "Multicentric plasma cell variant of Castleman's disease", "multicentric plasma cell variant of Castleman's disease", "Human herpesvirus-8-associated multicentric Castleman disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multicentric Castleman disease", "shortest_name_length": 3}
{"curie": "UMLS:C0160390", "names": ["injury liver", "liver injury", "Liver injury", "LIVER INJURY", "liver; injury", "injury; liver", "injuries liver", "hepatic trauma", "Hepatic trauma", "Hepatic injury", "hepatic injury", "injury hepatic", "Injury of liver", "injury of liver", "Injury to liver", "of liver injury", "Injury to Liver", "Hepatic injury, NOS", "Injury of liver, NOS", "Injury of liver (disorder)", "injury of liver (diagnosis)", "Unspecified injury of liver", "Injury of liver, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of liver", "shortest_name_length": 12}
{"curie": "MONDO:0016196", "names": ["qualitative or quantitative defects of emerin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of emerin", "shortest_name_length": 45}
{"curie": "UMLS:C0031142", "names": ["peritoneal disease", "Peritoneal Disease", "peritoneal disorder", "peritoneum diseases", "Peritoneal disorder", "Peritoneal Disorder", "peritoneal diseases", "Peritoneal Diseases", "Peritoneal Disorders", "Peritoneum--Diseases", "disorders peritoneum", "Disease of peritoneum", "Diseases of peritoneum", "Disorder of peritoneum", "Peritoneal disorder NOS", "disorders of peritoneum", "DISEASES OF THE PERITONEUM", "Disease of peritoneum, NOS", "Disorder of peritoneum (disorder)", "disease (or disorder); peritoneum", "Unspecified disorder of peritoneum", "disorders of peritoneum (diagnosis)", "Disorder of peritoneum, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peritoneal Diseases", "shortest_name_length": 18}
{"curie": "UMLS:C1707441", "names": ["Colorectal Small Cell Carcinoma", "Colorectal Small Cell Neuroendocrine Carcinoma", "Large Intestinal Small Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Small Cell Neuroendocrine Carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0009204", "names": ["faciocardiomelic dysplasia lethal", "Lethal faciocardiomelic dysplasia", "lethal faciocardiomelic dysplasia", "FACIOCARDIOMELIC DYSPLASIA, LETHAL", "faciocardiomelic dysplasia, lethal", "Faciocardiomelic Dysplasia, Lethal", "Lethal faciocardiomelic dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal faciocardiomelic dysplasia", "shortest_name_length": 33}
{"curie": "MONDO:0006122", "names": ["CNSET", "Calcifying nested epithelial stromal tumor", "Calcifying Nested Stromal-Epithelial Tumor", "Calcifying nested epithelial stromal tumour", "Calcifying Nested Epithelial Stromal Tumor of the Liver", "Calcifying Nested Stromal Epithelial Tumor of the Liver", "Calcifying Nested Stromal-Epithelial Tumor of the Liver", "calcifying nested epithelial stromal tumor of the liver", "Calcifying Nested Epithelial-Stromal Tumor of the Liver", "Calcifying nested epithelial stromal tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "calcifying nested epithelial stromal tumor of the liver", "shortest_name_length": 5}
{"curie": "MONDO:0004990", "names": ["breast tumor luminal", "luminal breast cancer", "luminal breast carcinoma", "Luminal A Breast Carcinoma", "luminal breast carcinoma A", "breast tumor luminal A or B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast tumor luminal A or B", "shortest_name_length": 20}
{"curie": "MONDO:0100494", "names": ["autosomal dominant titinopathy", "TTN-related myopathy, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant titinopathy", "shortest_name_length": 30}
{"curie": "MONDO:0005208", "names": ["Amelanotic melanoma", "skin amelanotic melanoma", "Amelanotic Skin Melanoma", "amelanotic skin melanoma", "Amelanotic Melanoma of Skin", "amelanotic melanoma of skin", "Amelanotic Cutaneous Melanoma", "Amelanotic Melanoma of the Skin", "amelanotic melanoma of the skin", "zone of skin amelanotic melanoma", "amelanotic malignant skin melanoma", "Amelanotic Malignant Skin Melanoma", "skin amelanotic malignant melanoma", "amelanotic melanoma of zone of skin", "Amelanotic Cutaneous (Skin) Melanoma", "amelanotic cutaneous (skin) melanoma", "Amelanotic malignant melanoma of skin", "amelanotic malignant melanoma of skin", "Amelanotic Malignant Melanoma of Skin", "amelanotic melanoma of skin (diagnosis)", "amelanotic malignant melanoma (of skin)", "Amelanotic Malignant Melanoma (of Skin)", "Amelanotic Malignant Melanoma of the Skin", "amelanotic malignant melanoma of the skin", "Amelanotic malignant melanoma of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amelanotic skin melanoma", "shortest_name_length": 19}
{"curie": "MONDO:0004438", "names": ["sporadic breast cancer", "Sporadic Breast Cancer", "Sporadic Breast Carcinoma", "sporadic breast carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sporadic breast cancer", "shortest_name_length": 22}
{"curie": "UMLS:C5557177", "names": ["Stage IIIC Cervical Cancer AJCC v9", "Stage IIIC Cervical Carcinoma AJCC v9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Cervical Cancer AJCC v9", "shortest_name_length": 34}
{"curie": "MONDO:0007496", "names": ["RDP", "DYT12", "Dyt12", "DYT-ATP1A3", "dystonia-12", "Dystonia 12", "dystonia 12", "DYSTONIA 12", "dystonia type 12", "DYT12 - dystonia 12", "ATP1A3 dystonic disorder", "Rapid onset dystonia parkinsonism", "rapid-onset dystonia-parkinsonism", "Rapid-onset dystonia-parkinsonism", "Rapid-Onset Dystonia Parkinsonism", "Rapid-Onset Dystonia-Parkinsonism", "dystonia-Parkinsonism, rapid-onset", "DYSTONIA-PARKINSONISM, RAPID-ONSET", "Dystonia-Parkinsonism, Rapid-Onset", "Rapid onset dystonia parkinsonism (disorder)", "dystonic disorder caused by mutation in ATP1A3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dystonia 12", "shortest_name_length": 3}
{"curie": "MONDO:0009876", "names": ["runt", "Dwarf", "dwarf", "DWARF", "runts", "dwarfs", "Nanism", "IGHD1A", "NANISM", "nanism", "RUNTING", "IGHD IA", "IGHD 1A", "DWARFISM", "dwarfism", "Nanasoma", "Dwarfism", "Nanosoma", "Nanosomia", "True dwarf", "Pure dwarf", "Dwarf, NOS", "Normal dwarf", "Dwarfism NOS", "True dwarfism", "Pure dwarfism", "Little person", "Dwarfism, NOS", "short stature", "Short stature", "Sexual dwarfism", "congenital IGHD", "Normal dwarfism", "primordial dwarf", "Primordial dwarf", "Dwarf, ateliotic", "Physiologic dwarf", "Ateliotic dwarfism", "PRIMORDIAL DWARFISM", "Primordial dwarfism", "dwarfism primordial", "Ateleiotic dwarfism", "primordial dwarfism", "Physiologic dwarfism", "PITUITARY DWARFISM I", "Severe short stature", "Pituitary dwarfism 1", "pituitary dwarfism 1", "Pituitary Dwarfism I", "DWARFISM, ATELEIOTIC", "pituitary dwarfism I", "Extreme short stature", "Short stature, severe", "short stature disorder", "Proportionate dwarfism", "Short stature, extreme", "Short stature disorder", "Dwarfism, proportionate", "Congenital IGHD type IA", "Constitutional dwarfism", "congenital IGHD type IA", "hereditary short stature", "dwarfism; constitutional", "constitutional; dwarfism", "Sexual ateliotic dwarfism", "SEXUAL ATELEIOTIC DWARFISM", "sexual ateleiotic dwarfism", "Sexual ateleiotic dwarfism", "constitutional short stature", "Constitutional short stature", "Idiopathic pituitary dwarfism", "Primordial dwarfism (disorder)", "stature; short, constitutional", "short; stature, constitutional", "Ateleiotic dwarfism (disorder)", "Primordial dwarfism (diagnosis)", "congenital isolated GH deficiency", "Short stature disorder (disorder)", "short stature disorder (diagnosis)", "Illig-type growth hormone deficiency", "Illig-type Growth hormone deficiency", "ILLIG type growth hormone deficiency", "ILLIG-TYPE GROWTH HORMONE DEFICIENCY", "Constitutional short stature (disorder)", "constitutional short stature (diagnosis)", "congenital isolated GH deficiency type IA", "Congenital isolated GH deficiency type IA", "isolated growth hormone deficiency type IA", "isolated growth hormone deficiency type 1A", "Isolated growth hormone deficiency type IA", "isolated growth hormone deficiency, type IA", "ISOLATED GROWTH HORMONE DEFICIENCY, TYPE IA", "Isolated growth hormone deficiency, type 1b", "Isolated Growth Hormone Deficiency, Type IA", "isolated Growth hormone deficiency, type 1A", "growth hormone deficiency, isolated, type IA", "congenital isolated growth hormone deficiency", "non-acquired isolated growth hormone deficiency", "Nanism due to growth hormone isolated deficiency", "Congenital isolated growth hormone deficiency type IA", "congenital isolated growth hormone deficiency type IA", "autosomal recessive isolated growth hormone deficiency", "Growth hormone deficiency, isolated autosomal recessive", "Growth hormone deficiency, isolated, autosomal recessive", "GROWTH HORMONE DEFICIENCY, ISOLATED, AUTOSOMAL RECESSIVE", "Hypopituitary dwarfism with normal sexual characteristics"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated growth hormone deficiency type IA", "shortest_name_length": 4}
{"curie": "UMLS:C1708993", "names": ["Biphasic Thymoma", "Metaplastic Thymoma", "Metaplastic thymoma", "Thymoma with Pseudosarcomatous Stroma", "Low Grade Thymic Metaplastic Carcinoma", "Metaplastic thymoma (morphologic abnormality)", "Mixed Polygonal and Spindle Cell Type Thymoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metaplastic thymoma", "shortest_name_length": 16}
{"curie": "MONDO:0001622", "names": ["mechanical lagophthalmos", "Mechanical lagophthalmos", "Mechanical lagophthalmos (disorder)", "mechanical lagophthalmos (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mechanical lagophthalmos", "shortest_name_length": 24}
{"curie": "UMLS:C0278489", "names": ["Breast Cancer Stage IIIA", "stage IIIA breast cancer", "Stage IIIA Breast Cancer", "breast cancer, stage IIIA", "Breast Carcinoma Stage IIIA", "Stage IIIA Breast Carcinoma", "Stage IIIA Breast Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Breast Carcinoma", "shortest_name_length": 24}
{"curie": "UMLS:C1707540", "names": ["Cutaneous Adult T-Cell Leukemia/Lymphoma", "Cutaneous Adult T-Cell Lymphoma/Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous Adult T-Cell Leukemia/Lymphoma", "shortest_name_length": 40}
{"curie": "UMLS:C0033922", "names": ["psychomotor disorder", "psychomotor; disorder", "psychomotor disorders", "Psychomotor Disorders", "disorder; psychomotor", "Psychomotor disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Psychomotor Disorders", "shortest_name_length": 20}
{"curie": "UMLS:C1333429", "names": ["EBV-Related Clonal PTLD", "EBV Related Clonal PTLD", "EBV-Related Clonal Post-Transplant Lymphoproliferative Disorder", "Epstein-Barr Virus-Related Clonal Post-Transplant Lymphoproliferative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "EBV-Related Clonal Post-Transplant Lymphoproliferative Disorder", "shortest_name_length": 23}
{"curie": "UMLS:C2983137", "names": ["Colon Carcinoma Metastatic in the Lung", "Colon Carcinoma Metastatic to the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colon Carcinoma Metastatic in the Lung", "shortest_name_length": 38}
{"curie": "UMLS:C4682589", "names": ["Stage IVB Uterine Corpus Adenosarcoma", "Stage IVB Uterine Corpus Adenosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Uterine Corpus Adenosarcoma AJCC v8", "shortest_name_length": 37}
{"curie": "UMLS:C2828036", "names": ["Stage IIIC Skin Melanoma AJCC v7", "Stage IIIC Cutaneous (Skin) Melanoma", "Stage IIIC Cutaneous Melanoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Cutaneous Melanoma AJCC v7", "shortest_name_length": 32}
{"curie": "MONDO:0019216", "names": ["transport; amino-acid", "amino-acid transport disorder", "Amino acid transport disorder", "AMINO ACID TRANSPORT DISORDERS", "disorder; amino-acid transport", "Disorder of Amino Acid Transport", "Disorder of amino acid transport", "Disorders of amino-acid transport", "Amino acid transport disorder, NOS", "Disturbances of amino-acid transport", "Disorder of amino acid transport, NOS", "inborn disorder of amino acid transport", "Amino acid transport disorder (disorder)", "amino-acid transport disorder (diagnosis)", "Disorders of amino-acid transport, unspecified", "disorder of amino acid absorption and transport", "Disorder of amino acid absorption and transport", "inborn disorder of amino acid absorption and transport"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of amino acid transport", "shortest_name_length": 21}
{"curie": "UMLS:C3540662", "names": ["Hereditary Retinal Aplasia", "Heredoretinopathia Congenitalis", "Dysgenesis Neuroepithelialis Retinae", "Congenital Amaurosis of Retinal Origin", "Hereditary Epithelial Dysplasia of Retina"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Amaurosis of Retinal Origin", "shortest_name_length": 26}
{"curie": "UMLS:C4055141", "names": ["Diffuse Endocapillary Glomerulonephritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse Endocapillary Glomerulonephritis", "shortest_name_length": 40}
{"curie": "UMLS:C1335427", "names": ["Plasmablastic Lymphoma of Mucosa Site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Plasmablastic Lymphoma of Mucosa Site", "shortest_name_length": 37}
{"curie": "MONDO:0018223", "names": ["systemic EBV+ T-cell LPD of childhood", "Systemic EBV+ T-cell LPD of childhood", "systemic EBV-positive T-cell lymphoma of childhood", "Systemic EBV-Positive T-Cell Lymphoma of Childhood", "EBV-positive T-cell lymphoproliferative disorder of childhood", "systemic Epstein-Barr virus positive T-cell lymphoma of childhood", "Systemic EBV-positive T-cell lymphoproliferative disease of childhood", "Systemic EBV positive T-cell lymphoproliferative disease of childhood", "Systemic EBV-Positive T-Cell Lymphoproliferative Disease of Childhood", "systemic EBV-positive T-cell lymphoproliferative disease of childhood", "systemic EBV-positive T-cell lymphoproliferative disorder of childhood", "Systemic EBV-Positive T-Cell Lymphoproliferative Disorder of Childhood", "Systemic Epstein Barr virus positive T-cell lymphoproliferative disease of childhood", "Systemic Epstein-Barr virus positive T-cell lymphoproliferative disease of childhood", "Systemic Epstein-Barr virus-positive T-cell lymphoproliferative disease of childhood", "systemic Epstein-Barr virus-positive T-cell lymphoproliferative disease of childhood", "Systemic Epstein-Barr virus positive T-cell lymphoproliferative disease of childhood (disorder)", "Systemic Epstein Barr virus positive T-cell lymphoproliferative disease of childhood (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "systemic Epstein-Barr virus-positive T-cell lymphoproliferative disease of childhood", "shortest_name_length": 37}
{"curie": "UMLS:C4682890", "names": ["Renal Pelvis and Ureter Cancer by AJCC v8 Stage", "Renal Pelvis and Ureter Urothelial Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal Pelvis and Ureter Cancer by AJCC v8 Stage", "shortest_name_length": 47}
{"curie": "UMLS:C4744334", "names": ["Locally Advanced Unresectable Renal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Unresectable Renal Cell Carcinoma", "shortest_name_length": 50}
{"curie": "MONDO:0030625", "names": ["DSKOR", "dyskinesia with orofacial involvement, autosomal recessive", "DYSKINESIA WITH OROFACIAL INVOLVEMENT, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyskinesia with orofacial involvement, autosomal recessive", "shortest_name_length": 5}
{"curie": "MONDO:0012183", "names": ["CMM3", "melanoma, cutaneous malignant, 3", "susceptibility to cutaneous malignant melanoma 3", "melanoma, cutaneous malignant, susceptibility to, 3", "MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 3", "melanoma, cutaneous malignant, susceptibility to, type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melanoma, cutaneous malignant, susceptibility to, 3", "shortest_name_length": 4}
{"curie": "UMLS:C4763749", "names": ["Platinum-Resistant Fallopian Tube Cancer", "Platinum-Resistant Fallopian Tube Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Platinum-Resistant Fallopian Tube Carcinoma", "shortest_name_length": 40}
{"curie": "UMLS:C4054602", "names": ["Lithium - Induced Nephropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lithium - Induced Nephropathy", "shortest_name_length": 29}
{"curie": "UMLS:C1336277", "names": ["stage III urethra cancer", "Stage III Urethra Cancer", "Urethra Cancer Stage III", "urethra cancer stage III", "Stage III Urethral Cancer", "stage III urethral cancer", "Stage III Urethra Carcinoma", "stage III urethra carcinoma", "Stage III Urethral Carcinoma", "stage III urethral carcinoma", "Stage III Carcinoma of Urethra", "stage III carcinoma of urethra", "Stage III Urethral Cancer AJCC v7", "stage III urethral cancer AJCC v7", "Stage III Carcinoma of the Urethra", "stage III carcinoma of the urethra"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Urethral Cancer AJCC v7", "shortest_name_length": 24}
{"curie": "UMLS:C4521722", "names": ["Stage IVB Esophageal Adenocarcinoma", "Postneoadjuvant Therapy Stage IVB Esophageal Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postneoadjuvant Therapy Stage IVB Esophageal Adenocarcinoma AJCC v8", "shortest_name_length": 35}
{"curie": "UMLS:C1707833", "names": ["Dura Mater Nick Cut Or Tear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dura Mater Nick Cut Or Tear", "shortest_name_length": 27}
{"curie": "MONDO:0035408", "names": ["furuncular myiasis due to Cordylobia rodhaini", "furunculoid myiasis due to Cordylobia rodhaini", "furunculous myiasis due to Cordylobia rodhaini"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "furuncular myiasis due to Cordylobia rodhaini", "shortest_name_length": 45}
{"curie": "MONDO:0023212", "names": ["Garret-Tripp syndrome", "Garret Tripp syndrome", "polydactyly alopecia seborrheic dermatitis", "Mental retardation with postaxial polydactyly, congenital absence of hair, severe seborrhoeic dermatitis, and Perthes' disease of the hip", "mental retardation with postaxial polydactyly, congenital absence of hair, severe seborrhoeic dermatitis, and Perthes' disease of the hip", "intellectual disability with postaxial polydactyly, congenital absence of hair, severe seborrhoeic dermatitis, and Perthes' disease of the hip", "Intellecutal disability with postaxial polydactyly, congenital absence of hair, severe seborrhoeic dermatitis, and Perthes' disease of the hip"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Garret-Tripp syndrome", "shortest_name_length": 21}
{"curie": "UMLS:C1336129", "names": ["Stage IB2 Cervical Cancer", "Cervical Cancer Stage IB2", "AJCC Stage IB2 Cervical Cancer", "FIGO Stage IB2 Cervix Carcinoma", "Stage IB2 Cervical Cancer AJCC v7", "Stage IB2 Cervical Cancer AJCC v6", "FIGO Stage IB2 Cervical Carcinoma", "FIGO Stage IB2 Carcinoma of Cervix", "FIGO Stage IB2 Cervix Uteri Carcinoma", "FIGO Stage IB2 Carcinoma of the Cervix", "FIGO Stage IB2 Uterine Cervix Carcinoma", "FIGO Stage IB2 Carcinoma of Cervix Uteri", "Stage IB2 Cervical Cancer AJCC v6 and v7", "FIGO Stage IB2 Carcinoma of Uterine Cervix", "FIGO Stage IB2 Carcinoma of the Cervix Uteri", "FIGO Stage IB2 Carcinoma of the Uterine Cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB2 Cervical Cancer", "shortest_name_length": 25}
{"curie": "MONDO:0022855", "names": ["congenital vagal hyperreflexivity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital vagal hyperreflexivity", "shortest_name_length": 33}
{"curie": "MONDO:0017770", "names": ["Robinow-like syndrome", "Saal-Greenstein syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Robinow-like syndrome", "shortest_name_length": 21}
{"curie": "UMLS:C1274469", "names": ["onychomycosis of fingernail", "onychomycosis of fingernail (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "onychomycosis of fingernail", "shortest_name_length": 27}
{"curie": "MONDO:0001680", "names": ["vaginal mullerian papilloma", "vaginal Mullerian papilloma", "Vaginal Müllerian Papilloma", "Vaginal Mullerian Papilloma", "vaginal Müllerian papilloma", "vaginal Muellerian papilloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vaginal mullerian papilloma", "shortest_name_length": 27}
{"curie": "UMLS:C0342648", "names": ["Extraosseous Calcification", "Extraosseous calcification", "Extraskeletal calcification", "Extraskeletal calcification (diagnosis)", "degenerative disorder extraskeletal calcification"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extraskeletal calcification", "shortest_name_length": 26}
{"curie": "UMLS:C0007781", "names": ["Intracranial Embolism and Thrombosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intracranial Embolism and Thrombosis", "shortest_name_length": 36}
{"curie": "UMLS:C5206598", "names": ["Paratesticular Leiomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paratesticular Leiomyosarcoma", "shortest_name_length": 29}
{"curie": "UMLS:C5555070", "names": ["Low Grade Peripheral Chondrosarcoma", "Low-Grade Peripheral Chondrosarcoma", "Secondary Peripheral Atypical Cartilaginous Tumor/Chondrosarcoma, Grade 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary Peripheral Atypical Cartilaginous Tumor/Chondrosarcoma, Grade 1", "shortest_name_length": 35}
{"curie": "UMLS:C4687512", "names": ["Locally Advanced Angiosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Angiosarcoma", "shortest_name_length": 29}
{"curie": "UMLS:C0432222", "names": ["SPENCD", "Spondyloenchondromatosis", "Spondyloenchondrodysplasia", "Spondyloenchondromatosis (disorder)", "Spondyloenchondrodysplasia (disorder)", "Spondylometaphyseal dysplasia with enchondromatous changes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spondyloenchondrodysplasia", "shortest_name_length": 6}
{"curie": "MONDO:0800031", "names": ["central hypoventilation syndrome, congenital"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central hypoventilation syndrome, congenital", "shortest_name_length": 44}
{"curie": "MONDO:0017839", "names": ["classic 21-OHD CAH, salt wasting form", "classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, salt wasting form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, salt wasting form", "shortest_name_length": 37}
{"curie": "MONDO:0009948", "names": ["HPP", "pyropoikilocytosis", "Pyropoikilocytosis", "PYROPOIKILOCYTOSIS", "Hereditary Pyropoikilocytosis", "pyropoikilocytosis hereditary", "Hereditary pyropoikilocytosis", "hereditary pyropoikilocytosis", "pyropoikilocytosis, hereditary", "PYROPOIKILOCYTOSIS, HEREDITARY", "Pyropoikilocytosis, Hereditary", "Pyropoikilocytosis, hereditary", "HPP - Hereditary pyropoikilocytosis", "Hereditary pyropoikilocytosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyropoikilocytosis, hereditary", "shortest_name_length": 3}
{"curie": "MONDO:0020798", "names": ["FIH2", "hypoparathyroidism, familial isolated 2", "hypoparathyroidism, familial isolated, 2", "HYPOPARATHYROIDISM, FAMILIAL ISOLATED, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypoparathyroidism, familial isolated, 2", "shortest_name_length": 4}
{"curie": "MONDO:0001907", "names": ["dermatomyositis", "Dermatomyositis NOS", "Adult dermatomyositis", "adult dermatomyositis", "Adult Dermatomyositis", "dermatomyositis of adults", "Adult Type Dermatomyositis", "Adult type dermatomyositis", "adult onset dermatomyositis", "Adult onset dermatomyositis", "Dermatomyositis, adult type", "Dermatomyositis, Adult Type", "Adult onset dermatomyositis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult dermatomyositis", "shortest_name_length": 15}
{"curie": "MONDO:0012319", "names": ["BPEO", "MAFD3", "MAJOR AFFECTIVE DISORDER 3", "Major Affective Disorder 3", "MAJOR affective disorder 3", "major affective disorder 3", "bipolar affective disorder, early-onset", "BIPOLAR AFFECTIVE DISORDER, EARLY-ONSET", "major affective disorder 3, early onset", "Bipolar Affective Disorder, Early-Onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "major affective disorder 3", "shortest_name_length": 4}
{"curie": "UMLS:C4682810", "names": ["Testicular Cancer by AJCC v6 and v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular Cancer by AJCC v6 and v7 Stage", "shortest_name_length": 41}
{"curie": "MONDO:0009888", "names": ["Polycystic Kidney, Cataract, and Congenital Blindness", "POLYCYSTIC KIDNEY, CATARACT, AND CONGENITAL BLINDNESS", "polycystic kidney, cataract, and congenital blindness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polycystic kidney, cataract, and congenital blindness", "shortest_name_length": 53}
{"curie": "MONDO:0008367", "names": ["HPCHA", "Leaky Red cell syndrome", "LEAKY RED CELL SYNDROME", "leaky Red cell syndrome", "RED CELL PHOSPHOLIPID DEFECT WITH HEMOLYSIS", "red cell phospholipid defect with hemolysis", "Red cell phospholipid defect with hemolysis", "PHOSPHATIDYLCHOLINE RED CELL MEMBRANE DISORDER", "phosphatidylcholine Red cell Membrane disorder", "Phosphatidylcholine Red cell membrane disorder", "HIGH RED CELL PHOSPHATIDYLCHOLINE HEMOLYTIC ANEMIA", "High red cell phosphatidylcholine hemolytic anemia", "high Red cell phosphatidylcholine hemolytic Anemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "red cell phospholipid defect with hemolysis", "shortest_name_length": 5}
{"curie": "UMLS:C5236010", "names": ["Advanced Genitourinary System Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Genitourinary System Carcinoma", "shortest_name_length": 39}
{"curie": "MONDO:0013990", "names": ["PCH8", "Pontocerebellar hypoplasia type 8", "pontocerebellar hypoplasia type 8", "pontocerebellar hypoplasia, type 8", "PONTOCEREBELLAR HYPOPLASIA, TYPE 8", "PCH8 - pontocerebellar hypoplasia type 8", "Congenital pontocerebellar hypoplasia type 8", "CHMP1A non-syndromic pontocerebellar hypoplasia", "Pontocerebellar hypoplasia due to CHMP1A mutation", "pontocerebellar hypoplasia due to CHMP1A mutation", "Congenital pontocerebellar hypoplasia type 8 (disorder)", "non-syndromic pontocerebellar hypoplasia caused by mutation in CHMP1A", "Pontocerebellar hypoplasia due to CHMP1A (charged multivesicular body protein 1A) mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pontocerebellar hypoplasia type 8", "shortest_name_length": 4}
{"curie": "MONDO:0007112", "names": ["Interventricular septum aneurysm", "interventricular septum aneurysm", "aneurysm; interventricular septum", "interventricular septum; aneurysm", "Aneurysm Of Interventricular Septum", "ANEURYSM OF INTERVENTRICULAR SEPTUM", "aneurysm of interventricular septum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "interventricular septum aneurysm", "shortest_name_length": 32}
{"curie": "UMLS:C5439527", "names": ["MIS-A", "Multisystem Inflammatory Syndrome in Adults", "Multisystem inflammatory syndrome in adults", "MIS-A - multisystem inflammatory syndrome in adults", "Multisystem inflammatory syndrome in adults (disorder)", "Adult inflammatory multisystem syndrome temporally associated with COVID-19"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Multisystem inflammatory syndrome in adults", "shortest_name_length": 5}
{"curie": "MONDO:0002766", "names": ["larynx verrucous carcinoma", "Larynx Verrucous Carcinoma", "Verrucous carcinoma of larynx", "Laryngeal verrucous carcinoma", "Laryngeal Verrucous Carcinoma", "Verrucous Carcinoma of Larynx", "verrucous carcinoma of larynx", "laryngeal verrucous carcinoma", "verrucous carcinoma, laryngeal", "verrucous carcinoma of the larynx", "laryngeal throat verrucous cancer", "Laryngeal Throat Verrucous Cancer", "Verrucous Carcinoma of the Larynx", "verrucous carcinoma of the Larynx", "Primary verrucous carcinoma of larynx", "verrucous carcinoma of larynx (diagnosis)", "Primary verrucous carcinoma of larynx (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "larynx verrucous carcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0018461", "names": ["Angelman syndrome due to a point mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Angelman syndrome due to a point mutation", "shortest_name_length": 41}
{"curie": "UMLS:C3489732", "names": ["Familial mesangial sclerosis", "familial mesangial sclerosis", "Mesangial Sclerosis, Familial", "nephrotic syndrome congenital type 3", "Familial mesangial sclerosis (disorder)", "familial mesangial sclerosis (diagnosis)", "nephrotic syndrome congenital type 3 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Familial mesangial sclerosis", "shortest_name_length": 28}
{"curie": "UMLS:C0333536", "names": ["GANGRENE DRY", "dry gangrene", "gangrene dry", "Dry gangrene", "Gangrene, dry", "mummification", "dry gangrene (ischemic)", "dry gangrene (diagnosis)", "dry gangrene (physical finding)", "Dry gangrene (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dry gangrene", "shortest_name_length": 12}
{"curie": "MONDO:0005975", "names": ["Purulent otitis media", "OTITIS MEDIA PURULENT", "purulent otitis media", "Purulent Otitis Media", "Otitis Media, Purulent", "middle ear; suppuration", "suppuration; middle ear", "EAR SUPPURATION, MIDDLE", "otitis; media, purulent", "suppurative otitis media", "media otitis suppurative", "otitis media suppurative", "Suppurative Otitis Media", "Suppurative otitis media", "Otitis media suppurative", "Otitis Media, Suppurative", "Purulent otitis media NOS", "suppurative; otitis media", "otitis; media, suppurative", "Purulent otitis media, NOS", "Otitis media suppurative NOS", "Suppurative otitis media, NOS", "Purulent otitis media (disorder)", "Unspecified suppurative otitis media", "suppurative otitis media (diagnosis)", "Otitis media with effusion - purulent", "otitis media with effusion - purulent", "Suppurative otitis media, unspecified", "Suppurative and unspecified otitis media", "Suppurative otitis media, unspecified, unspecified ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "suppurative otitis media", "shortest_name_length": 21}
{"curie": "UMLS:C4528582", "names": ["Stage IIA Breast Cancer", "Prognostic Stage IIA Breast Cancer AJCC v8", "Prognostic Stage IIA Breast Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prognostic Stage IIA Breast Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "MONDO:0007319", "names": ["CPPDD", "CCAL2", "CPPDD2", "familial CC", "CALCIUM GOUT", "Calcium Gout", "calcium gout", "familial CPPD", "hereditary CC", "chondrocalcinosis 2", "CHONDROCALCINOSIS 2", "Chondrocalcinosis 2", "Pseudogout, familial", "calcium gout, familial", "chondrocalcinosis type 2", "calcium pyrophosphate arthropathy", "Calcium Pyrophosphate Arthropathy", "Calcium pyrophosphate arthropathy", "CALCIUM PYROPHOSPHATE ARTHROPATHY", "chondrocalcinosis familial articular", "familial articular chondrocalcinosis", "Chondrocalcinosis, Familial Articular", "chondrocalcinosis, familial articular", "CHONDROCALCINOSIS, FAMILIAL ARTICULAR", "hereditary articular chondrocalcinosis", "familial calcium pyrophosphate deposition", "hereditary calcium pyrophosphate deposition", "calcium pyrophosphate arthropathy, familial", "Calcium Pyrophosphate Dihydrate Deposition Disease", "calcium pyrophosphate dihydrate deposition disease", "Calcium pyrophosphate dihydrate deposition disease", "CALCIUM PYROPHOSPHATE DIHYDRATE DEPOSITION DISEASE", "CALCIUM PYROPHOSPHATE DIHYDRATE DEPOSITION DISEASE 2", "CPPDD Calcium Pyrophosphate Dihydrate Deposition Disease", "calcium pyrophosphate dihydrate crystal deposition disease", "familial calcium pyrophosphate dihydrate deposition disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chondrocalcinosis 2", "shortest_name_length": 5}
{"curie": "MONDO:0017860", "names": ["methanol poisoning"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "methanol poisoning", "shortest_name_length": 18}
{"curie": "MONDO:0026726", "names": ["NPHS20", "nephrotic syndrome type 20", "nephrotic syndrome, type 20", "NEPHROTIC SYNDROME, TYPE 20"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrotic syndrome, type 20", "shortest_name_length": 6}
{"curie": "MONDO:0017698", "names": ["GSDIV, congenital neuromuscular form", "GSD IV, Neuromuscular Form, Congenital", "GSD IV, NEUROMUSCULAR FORM, CONGENITAL", "GSD type 4, congenital neuromuscular form", "GBE deficiency, congenital neuromuscular form", "Glycogenosis type 4, congenital neuromuscular form", "glycogenosis type 4, congenital neuromuscular form", "Glycogenosis type IV, congenital neuromuscular form", "glycogenosis type IV, congenital neuromuscular form", "Glycogen storage disease type 4, congenital neuromuscular form", "glycogen storage disease type 4, congenital neuromuscular form", "glycogen storage disease type IV, congenital neuromuscular form", "Glycogen storage disease type IV, congenital neuromuscular form", "GSD due to glycogen branching enzyme deficiency, congenital neuromuscular form", "Glycogenosis due to glycogen branching enzyme deficiency, congenital neuromuscular form", "glycogenosis due to glycogen branching enzyme deficiency, congenital neuromuscular form", "glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form", "Glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form", "shortest_name_length": 36}
{"curie": "UMLS:C5666829", "names": ["DGONC", "Diffuse Glioneuronal Tumor with Oligodendroglioma-Like Features and Nuclear Clusters"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse Glioneuronal Tumor with Oligodendroglioma-Like Features and Nuclear Clusters", "shortest_name_length": 5}
{"curie": "UMLS:C4055503", "names": ["Acquired Cytomegaloviral Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired Cytomegaloviral Infection", "shortest_name_length": 34}
{"curie": "MONDO:0003777", "names": ["renal pelvis urothelial papilloma", "Renal Pelvis Urothelial Papilloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal pelvis urothelial papilloma", "shortest_name_length": 33}
{"curie": "UMLS:C3897225", "names": ["Untreated Oligodendroglioma", "Untreated Childhood Oligodendroglioma", "untreated childhood oligodendroglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Untreated Childhood Oligodendroglioma", "shortest_name_length": 27}
{"curie": "UMLS:C3898830", "names": ["Hypersexualism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypersexualism", "shortest_name_length": 14}
{"curie": "UMLS:C0423682", "names": ["mechanical low back pain", "Mechanical low back pain", "Mechanical Low Back Pain", "Low Back Pain, Mechanical", "mechanical lower back pain", "lower back pain mechanical", "Mechanical low back pain (finding)", "mechanical lower back pain (symptom)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Back Pain, Mechanical", "shortest_name_length": 24}
{"curie": "UMLS:C5420318", "names": ["Transfusion Dependent Beta Thalassemia", "Transfusion-dependent Beta Thalassemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transfusion Dependent Beta Thalassemia", "shortest_name_length": 38}
{"curie": "MONDO:0020757", "names": ["sporadic hemiplegic migraine", "Sporadic Hemiplegic Migraine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sporadic hemiplegic migraine", "shortest_name_length": 28}
{"curie": "MONDO:0005267", "names": ["Cardiopathy", "cardiopathy", "RNDx cardiac", "heart disease", "heart trouble", "Disease;heart", "Morbus cordis", "Heart disease", "Heart Disease", "morbus cordis", "HEART DISEASE", "Heart trouble", "cardiopathies", "HEART DISEASES", "disorder heart", "Heart Disorder", "morbus; cordis", "Heart disorder", "Heart Diseases", "disease hearts", "heart diseases", "heart disorder", "HEART DISORDER", "cordis; morbus", "cardiac disease", "disease cardiac", "Cardiac Disease", "Heart--Diseases", "Heart Disorders", "heart disorders", "disease of heart", "Cardiac disorder", "cardiac disorder", "Cardiac diseases", "Cardiopathy, NOS", "cardiac diseases", "Cardiac Diseases", "Cardiac Disorder", "disorder of heart", "Disorder of heart", "Cardiac Disorders", "cardiac disorders", "Morbus cordis NOS", "Heart disease NOS", "Cardiac disorders", "Heart disease, NOS", "Morbus cordis, NOS", "HEART DISEASE, NOS", "Cardiac disorder NOS", "Diseases of the heart", "diseases of the heart", "DISORDER CARDIAC (NOS)", "heart disease disorder", "syndrome heart disease", "Disorder cardiac (NOS)", "disease disorders heart", "diseases disorders heart", "RNDx cardiac (diagnosis)", "Heart disease (disorder)", "heart/pericardial disease", "Unspecified Heart Problem", "heart disease (diagnosis)", "heart/pericardial trouble", "heart disease or disorder", "heart/pericardial disorder", "Heart disease, unspecified", "disease or disorder of heart", "Disease or syndrome of heart", "disorder of heart/pericardium", "HEART DISEASES: GENERAL TERMS", "Diseases and Syndromes of Heart", "heart/pericardial disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heart disorder", "shortest_name_length": 11}
{"curie": "MONDO:0006929", "names": ["Proteus", "infection proteus", "Proteus infection", "Proteus Infection", "proteus infection", "Infection, Proteus", "proteus infections", "Proteus; infection", "Proteus infections", "Proteus Infections", "infection; Proteus", "infection, Proteus", "Infections, Proteus", "infections, Proteus", "Proteus infection NOS", "Proteus infectious disease", "Proteus infection (disorder)", "Proteus <enterobacteria> infectious disease", "Proteus <enterobacteria> disease or disorder", "Proteus <enterobacteria> caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Proteus infectious disease", "shortest_name_length": 7}
{"curie": "UMLS:C1336109", "names": ["Stage IA1 Cervical Cancer", "Cervical Cancer Stage IA1", "AJCC Stage IA1Cervical Cancer", "FIGO Stage IA1 Cervix Carcinoma", "Stage IA1 Cervical Cancer AJCC v6", "Stage IA1 Cervical Cancer AJCC v7", "FIGO Stage IA1 Cervical Carcinoma", "FIGO Stage IA1 Carcinoma of Cervix", "FIGO Stage IA1 Cervix Uteri Carcinoma", "FIGO Stage IA1 Carcinoma of the Cervix", "FIGO Stage IA1 Uterine Cervix Carcinoma", "Stage IA1 Cervical Cancer AJCC v6 and v7", "FIGO Stage IA1 Carcinoma of Cervix Uteri", "FIGO Stage IA1 Carcinoma of Uterine Cervix", "FIGO Stage IA1 Carcinoma of the Cervix Uteri", "FIGO Stage IA1 Carcinoma of the Uterine Cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA1 Cervical Cancer", "shortest_name_length": 25}
{"curie": "UMLS:C4086172", "names": ["Childhood Small Intestine Leiomyosarcoma", "Childhood Small Intestinal Leiomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Small Intestinal Leiomyosarcoma", "shortest_name_length": 40}
{"curie": "MONDO:0007469", "names": ["fifth toe, double nails", "double nail for fifth toe", "Double Nail for Fifth Toe", "DOUBLE NAIL FOR FIFTH TOE", "Double nails on the fifth toe"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "double nail for fifth toe", "shortest_name_length": 23}
{"curie": "MONDO:0700001", "names": ["SLS", "small lungs", "shrinking of the lung", "shrinking lung syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "shrinking lung syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0011560", "names": ["SLEB3", "SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 3", "systemic lupus erythematosus, susceptibility to, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "systemic lupus erythematosus, susceptibility to, 3", "shortest_name_length": 5}
{"curie": "UMLS:C0521621", "names": ["Solitary Multilocular Renal Cyst", "Solitary multilocular renal cyst", "Solitary Multilocular Kidney Cyst", "Acquired solitary multilocular renal cyst"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired solitary multilocular renal cyst", "shortest_name_length": 32}
{"curie": "UMLS:C1334998", "names": ["Non-Neoplastic Breast Disease", "Non-Neoplastic Breast Disorder", "Non-Neoplastic Disease of Breast", "Non-Neoplastic Disease of the Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Breast Disorder", "shortest_name_length": 29}
{"curie": "MONDO:0016505", "names": ["APAC", "Pure APAC", "aldosterone-producing adenoma", "Aldosterone-Producing Adrenal Gland Adenoma", "Aldosterone-Producing Adrenal Cortex Adenoma", "Aldosterone Producing Adrenal Cortex Adenoma", "aldosterone-producing adrenal cortex adenoma", "aldosterone producing adrenal cortex adenoma", "Aldosterone Producing Adrenal Cortical Adenoma", "aldosterone producing adrenal cortical adenoma", "Aldosterone-Producing Adrenal Cortical Adenoma", "Pure aldosterone-secreting adrenocortical carcinoma", "Pure aldosterone-producing adrenocortical carcinoma", "adrenocortical carcinoma with pure aldosterone hypersecretion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aldosterone-producing adrenal cortex adenoma", "shortest_name_length": 4}
{"curie": "UMLS:C5670029", "names": ["GI Adhesions", "Gastrointestinal Adhesion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal Adhesion", "shortest_name_length": 12}
{"curie": "MONDO:0001149", "names": ["Nanocephaly", "microcephali", "Microcephaly", "microcephaly", "MICROCEPHALY", "Micrencephaly", "microcephalic", "micrencephala", "microcephalus", "Microcephalic", "micrencephaly", "Microcephalus", "Microcephalies", "micrencephalon", "microencephaly", "microcephalies", "Microencephaly", "microcephaly (disease)", "microcephaly (diagnosis)", "microcephalus (diagnosis)", "Isolated congenital microcephaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly", "shortest_name_length": 11}
{"curie": "MONDO:0009005", "names": ["C1r/C1s Deficiency", "C1r/C1s DEFICIENCY", "C1r/C1s deficiency", "complement component C1r/C1s deficiency", "COMPLEMENT COMPONENT C1r/C1s DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complement component C1r/C1s deficiency", "shortest_name_length": 18}
{"curie": "UMLS:C4727283", "names": ["Locally Advanced Unresectable Soft Tissue Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Unresectable Soft Tissue Sarcoma", "shortest_name_length": 49}
{"curie": "MONDO:0003441", "names": ["dystonia", "Dystonia", "DYSTONIA", "Dystonias", "dystonias", "Muscle Dystonia", "dystonic disease", "Dystonia, Muscle", "Dystonic disease", "dystonic disorder", "dystonia disorder", "Dystonia Disorder", "Dystonia disorder", "Dystonic Disorder", "Dystonic movements", "Dystonia Disorders", "dystonic disorders", "Dystonic Disorders", "dystonia disorders", "dystonia was noted", "dystonic movements", "Dystonia (disorder)", "dystonia (diagnosis)", "Dystonia, unspecified", "dystonia (physical finding)", "involuntary twisting movements", "abnormal muscle twitching or contraction", "involuntary twisting movements (symptom)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dystonic disorder", "shortest_name_length": 8}
{"curie": "MONDO:0006007", "names": ["reflux; ureter", "ureter; reflux", "Ureteral reflux", "Ureteric reflux", "ureteric reflux", "Reflux;ureteric", "VESICOURETER REFLUX", "Vesicoureteric reflux", "Vesicoureteral-reflux", "Vesicoureteral reflux", "vesicoureteral reflux", "vesicoureteric reflux", "Vesicoureteric Reflux", "Vesicoureteral Reflux", "reflux vesicoureteral", "reflux vesicoureteric", "vesicoureteral; reflux", "reflux; vesicoureteral", "REFLUX, VESICOURETERAL", "vesico-ureteric reflux", "vesico ureteral reflux", "Reflux, Vesicoureteral", "Vesico-ureteral reflux", "Vesico Ureteral Reflux", "Vesico-ureteric reflux", "Vesico-Ureteral Reflux", "vesico-ureteral reflux", "Reflux, Vesico-Ureteral", "Vesicoureteral-reflux NOS", "VUR - Vesicoureteric reflux", "VUR - Vesicoureteral Reflux", "regurgitation; vesicoureteral", "vesicoureteral; regurgitation", "vesicoureteral reflux (disease)", "Vesicoureteric reflux (disorder)", "vesicoureteral reflux (diagnosis)", "Vesicoureteral-reflux, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vesicoureteral reflux", "shortest_name_length": 14}
{"curie": "MONDO:0005092", "names": ["signet ring carcinoma", "Signet ring carcinoma", "Signet Ring Cell Carcinoma", "carcinoma signet ring cell", "Signet-Ring Cell Carcinoma", "Signet-ring cell carcinoma", "signet-ring cell carcinoma", "Signet ring cell carcinoma", "signet ring cell carcinoma", "Carcinoma, Signet Ring Cell", "Signet Ring Cell Adenocarcinoma", "signet ring cell adenocarcinoma", "Signet ring cell adenocarcinoma", "adenocarcinoma cells ring signet", "signet ring cell carcinoma (diagnosis)", "signet ring carcinoma NOS (morphologic abnormality)", "Signet ring cell carcinoma (morphologic abnormality)", "signet ring cell carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "signet ring cell carcinoma", "shortest_name_length": 21}
{"curie": "MONDO:0006610", "names": ["Atrophic", "ATROPHY SKIN", "Atrophoderma", "skin atrophy", "Skin atrophy", "SKIN ATROPHY", "Skin Atrophy", "Atrophy skin", "atrophoderma", "skin; atrophy", "Atrophic skin", "atrophic skin", "atrophy; skin", "Atrophic Skin", "Dermal atrophy", "atrophy - skin", "Atrophy - skin", "Atrophy of Skin", "Atrophy of skin", "atrophy of skin", "Atrophoderma, NOS", "Skin degeneration", "Atrophy of skin, NOS", "atrophoderma (diagnosis)", "skin; disorder, atrophic", "atrophic disorder of skin", "Atrophic condition of skin", "Atrophic disorders of skin", "atrophic condition of skin", "Atrophic condition of skin, NOS", "disease (or disorder); skin, atrophic", "Atrophic condition of skin (disorder)", "atrophic disorder of skin (diagnosis)", "Atrophic disorder of skin, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin atrophy", "shortest_name_length": 8}
{"curie": "MONDO:0020658", "names": ["infiltrating ureter transitional cell carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infiltrating ureter transitional cell carcinoma", "shortest_name_length": 47}
{"curie": "MONDO:0018941", "names": ["furuncular myiasis", "Furuncular myiasis", "Furunculous myiasis", "furunculous myiasis", "furunculoid myiasis", "Furunculoid myiasis", "Furuncular myiasis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "furuncular myiasis", "shortest_name_length": 18}
{"curie": "UMLS:C5669887", "names": ["Metastatic Malignant Mesonephroma", "Metastatic Mesonephric Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Mesonephric Adenocarcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C3273142", "names": ["Extrahepatic Bile Duct MANEC", "Extrahepatic Bile Duct Mixed Adenoneuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extrahepatic Bile Duct Mixed Adenoneuroendocrine Carcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0006877", "names": ["ovaritis", "OVARITIS", "OOPHORITIS", "oophoritis", "Oophoritis", "Oophoritides", "Oophoritis, NOS", "Inflammed ovary", "inflammation ovary", "Ovary inflammation", "ovary inflammation", "ovary; inflammation", "OVARY, INFLAMMATION", "inflammation; ovary", "inflammation ovaries", "inflammation of ovary", "Inflammation of ovary", "Oophoritis (disorder)", "oophoritis (diagnosis)", "Oophoritis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oophoritis", "shortest_name_length": 8}
{"curie": "UMLS:C1518357", "names": ["Non-Hodgkin's Lymphoma, Lymphoblastic (WF)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Hodgkin's Lymphoma, Lymphoblastic (WF)", "shortest_name_length": 42}
{"curie": "MONDO:0009811", "names": ["osteoma of middle ear", "OSTEOMA OF MIDDLE EAR", "Osteoma of Middle Ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteoma of middle ear", "shortest_name_length": 21}
{"curie": "UMLS:C1879328", "names": ["totally blind", "Blind both eyes", "total blindness", "BLINDNESS TOTAL", "Blindness, total", "total vision loss", "Complete Blindness", "complete blindness", "Bilateral Blindness", "Blindness, Complete", "Bilateral blindness", "total loss of vision", "Blindness, Bilateral", "Blindness, bilateral", "Blindness, both eyes", "Blindness - both eyes", "Bilateral Blindnesses", "loss; vision, both eyes", "vision; loss, both eyes", "total vision loss binocular", "total blindness in both eyes", "total vision loss in both eyes", "total loss of vision (symptom)", "Blindness - both eyes (disorder)", "Total loss of vision in both eyes", "total loss of vision in both eyes", "Both eyes total visual impairment", "Blindness both eyes NOS (disorder)", "total visual impairment of both eyes", "total loss of vision in both eyes (symptom)", "total visual impairment of both eyes (diagnosis)", "Blindness of both eyes, impairment level not further specified", "Profound impairment, both eyes, impairment level not further specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Blindness both eyes NOS (disorder)", "shortest_name_length": 13}
{"curie": "UMLS:C0238113", "names": ["radiation esophagitis", "Radiation esophagitis", "Radiation oesophagitis", "ESOPHAGITIS, IRRADIATION", "Radiation ulcerative esophagitis", "Radiation esophagitis (disorder)", "radiation esophagitis (diagnosis)", "Radiation ulcerative oesophagitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radiation esophagitis", "shortest_name_length": 21}
{"curie": "UMLS:C3887517", "names": ["Brain Stem Gliosarcoma", "childhood brainstem gliosarcoma", "childhood brain stem gliosarcoma", "Childhood Brain Stem Gliosarcoma", "gliosarcoma, childhood brain stem"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Brain Stem Gliosarcoma", "shortest_name_length": 22}
{"curie": "MONDO:0004450", "names": ["Occlusion carotid", "Carotid occlusion", "occlusion carotid", "OCCLUSION CAROTID", "carotid occlusion", "CAROTID OCCLUSION", "a.carotis; occlusion", "carotid artery occlusion", "occlusion carotid artery", "Carotid artery occlusion", "artery carotid occlusion", "occlusion; carotid artery", "Obstructed carotid artery", "arteries carotid occlusion", "carotid artery obstruction", "Carotid artery obstruction", "artery carotid obstruction", "Occlusion of carotid artery", "carotid artery occlusion (diagnosis)", "Carotid artery obstruction (disorder)", "carotid artery obstruction (diagnosis)", "Occlusion of carotid artery (disorder)", "Occlusion and stenosis of carotid artery", "occlusion and stenosis of carotid artery", "carotid artery segment occlusion precerebral artery", "occlusion precerebral artery of carotid artery segment", "Occlusion and stenosis of carotid artery without mention of cerebral infarction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carotid artery occlusion", "shortest_name_length": 17}
{"curie": "UMLS:C4527413", "names": ["Visceral Crisis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Visceral Crisis", "shortest_name_length": 15}
{"curie": "MONDO:0000458", "names": ["Proneural Glioblastoma", "proneural glioblastoma", "glioblastoma proneural subtype"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "proneural glioblastoma", "shortest_name_length": 22}
{"curie": "MONDO:0011661", "names": ["IBD5", "inflammatory bowel disease 5", "Inflammatory Bowel Disease 5", "INFLAMMATORY BOWEL DISEASE 5", "inflammatory bowel disease type 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory bowel disease 5", "shortest_name_length": 4}
{"curie": "UMLS:C0947700", "names": ["Neonatal leukopenia", "Leukopenia neonatal", "Neonatal Leukopenia", "LEUCOPENIA NEONATAL", "Leucopenia neonatal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leukopenia neonatal", "shortest_name_length": 19}
{"curie": "UMLS:C0853334", "names": ["Thrombocytopenia aggravated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thrombocytopenia aggravated", "shortest_name_length": 27}
{"curie": "MONDO:0005046", "names": ["immune disease", "Immune Disease", "immune disorder", "Immune Diseases", "Immune disorder", "Disease, Immune", "Immune Disorder", "disorder; immune", "Immune Disorders", "immune; disorder", "immune dysfunction", "Immunity disorders", "Immune disease NOS", "Immune Dysfunction", "Immune dysfunction", "immunologic disease", "Immunologic Disease", "immunologic disorder", "immunologic diseases", "Immune disorder, NOS", "Immunologic Disorder", "Disease, Immunologic", "Immunologic diseases", "Immunologic Diseases", "immunological disease", "Immune System Disease", "Immunological Disease", "Immune disorder (NOS)", "immunologic disorders", "IMMUNE DISORDER (NOS)", "Immunologic Disorders", "immune system disease", "immunological diseases", "Immune System Diseases", "Immunological Diseases", "Immune System Disorder", "Disease, Immunological", "immune system disorder", "IMMUNE SYSTEM DISORDER", "Immune system disorder", "immune system diseases", "Disease, Immune System", "Immune System Disorders", "Immune system disorders", "Disorder, Immune System", "disease of immune system", "Disorder of immune system", "disorder of immune system", "Disorder of Immune System", "Diseases of Immune System", "Immune system disorder NOS", "Disorder of immune function", "Immune System and Disorders", "Immune system disorder (NOS)", "IMMUNE SYSTEM DISORDER (NOS)", "Disorder immune system (NOS)", "DISORDER IMMUNE SYSTEM (NOS)", "DISEASES OF THE IMMUNE SYSTEM", "Disease of immune system, NOS", "Disorder of immune system, NOS", "immune system disease or disorder", "immunologic disorders (diagnosis)", "Unspecified Immune System Problem", "disease or disorder of immune system", "Disorder of immune function (disorder)", "Disorders involving the immune mechanism", "Unspecified disorder of immune mechanism", "DISEASES OF THE IMMUNE SYSTEM: GENERAL TERMS", "Disorder of immune system (navigational concept)", "Disorder involving the immune mechanism, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immune system disorder", "shortest_name_length": 14}
{"curie": "MONDO:0018328", "names": ["HoFH", "homozygous familial hypercholesterolemia", "Homozygous familial hypercholesterolemia", "Homozygous Familial Hypercholesterolemia", "Familial homozygous hypercholesterolemia", "Homozygous familial hypercholesterolaemia", "Familial homozygous hypercholesterolaemia", "Familial hypercholesterolemia - homozygous", "Hypercholesterolemias, Homozygous Familial", "Familial hypercholesterolaemia - homozygous", "homozygous familial hypercholesterolemia (diagnosis)", "Familial hypercholesterolemia - homozygous (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "homozygous familial hypercholesterolemia", "shortest_name_length": 4}
{"curie": "MONDO:0001434", "names": ["inflammatory spondylopathy", "inflammatory spondylopathies in disease EC", "Inflammatory spondylopathies in disease EC", "inflammatory spondylopathy in disease classified elsewhere", "Inflammatory spondylopathy in disease classified elsewhere", "inflammatory spondylopathies in disease classified elsewhere", "Inflammatory spondylopathies in disease classified elsewhere", "Inflammatory spondylopathies in diseases classified elsewhere", "inflammatory spondylopathies in diseases classified elsewhere", "inflammatory spondylopathies in diseases classified elsewhere (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory spondylopathy", "shortest_name_length": 26}
{"curie": "UMLS:C4521644", "names": ["stage IVA esophageal cancer", "Stage IVA Esophageal Adenocarcinoma", "clinical stage IVA esophageal adenocarcinoma AJCC v8", "Clinical Stage IVA Esophageal Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage IVA Esophageal Adenocarcinoma AJCC v8", "shortest_name_length": 27}
{"curie": "UMLS:C4524966", "names": ["stage III small intestine cancer", "Stage III Small Intestinal Adenocarcinoma", "stage III small intestinal adenocarcinoma AJCC v8", "Stage III Small Intestinal Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Small Intestinal Adenocarcinoma AJCC v8", "shortest_name_length": 32}
{"curie": "MONDO:0014439", "names": ["BBS11", "Bardet-Biedl syndrome 11", "BARDET-BIEDL SYNDROME 11", "Bardet-Biedl Syndrome 11", "TRIM32 Bardet-Biedl syndrome", "Bardet-Biedl syndrome type 11", "Bardet-Biedl syndrome caused by mutation in TRIM32"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bardet-Biedl syndrome 11", "shortest_name_length": 5}
{"curie": "MONDO:0011785", "names": ["SPG19", "spastic paraplegia 19", "hereditary spastic paraplegia 19", "hereditary spastic paraplegia type 19", "autosomal dominant spastic paraplegia 19", "spastic paraplegia 19, autosomal dominant", "SPASTIC PARAPLEGIA 19, AUTOSOMAL DOMINANT", "Spastic paraplegia 19, autosomal dominant", "autosomal dominant spastic paraplegia type 19", "Autosomal dominant spastic paraplegia type 19", "SPASTIC PARAPLEGIA 19, AUTOSOMAL DOMINANT (disorder)", "familial spastic paraplegia autosomal dominant type 19", "Autosomal dominant spastic paraplegia type 19 (disorder)", "Autosomal dominant spastic paraplegia type 19 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 19", "shortest_name_length": 5}
{"curie": "MONDO:0007915", "names": ["SLE", "sles", "lupus", "LUPUS", "SLE NOS", "LE syndrome", "LE systemic", "le syndrome", "LE SYNDROME", "les syndrome", "excess LMW-DNA", "SYNDROME LUPUS", "Lupus syndrome", "LUPUS SYNDROME", "Syndrome lupus", "lupus syndrome", "EXCESS LMW-DNA", "syndrome lupus", "lupus syndromes", "lupus erythematosis", "LUPUS ERYTHEMATOSIS (NOS)", "system; lupus erythematosus", "SYSTEMIC LUPUS ERYTHEMATOSIS", "Systemic Lupus Erythematosus", "systemic lupus erythematosus", "Systemic lupus erythematosus", "Lupus erythematosus systemic", "Systemic lupus erythematosis", "LUPUS ERYTHEMATOSUS SYSTEMIC", "erythematosis lupus systemic", "SYSTEMIC LUPUS ERYTHEMATOSUS", "Lupus Erythematosus, Systemic", "LUPUS ERYTHEMATOSUS, SYSTEMIC", "Lupus erythematosus, Systemic", "Lupus erythematosus, systemic", "Lupus Erythematosus, systemic", "lupus erythematosus, systemic", "lupus; erythematosus, systemic", "erythematosus; lupus, systemic", "LUPUS, ERYTHEMATOSUS, SYSTEMIC", "Disseminated lupus erythematosus", "Lupus Erythematosus Disseminatus", "DISSEMINATED LUPUS ERYTHEMATOSUS", "Systemic lupus erythematosus NOS", "disseminated lupus erythematosus", "Lupus erythematosis disseminated", "LUPUS ERYTHEMATOSIS DISSEMINATED", "lupus erythematosus disseminatus", "SYSTEMIC LUPUS ERYTHEMATOSUS SYND", "LUPUS ERYTHEMATOSUS, DISSEMINATED", "Lupus erythematosus, disseminated", "Systemic lupus erythematosus synd", "Systemic lupus erythematosus (SLE)", "SLE - Systemic lupus erythematosus", "lupus nephritis, susceptibility to", "systemic lupus erythematosus (SLE)", "SLE - Lupus Erythematosus, systemic", "SLE - lupus erythematosus, systemic", "SLE - Lupus Erythematosus, Systemic", "obsolete_systemic lupus erythematosus", "systemic lupus erythematosus (disease)", "Systemic lupus erythematosus (disorder)", "systemic lupus erythematosus (diagnosis)", "Systemic lupus erythematosus, unspecified", "Syndrome disseminated lupus erythematosis", "SYNDROME DISSEMINATED LUPUS ERYTHEMATOSIS", "EXCESS LYMPHOCYTE LOW MOLECULAR WEIGHT DNA", "excess lymphocyte low molecular weight DNA", "systemic lupus erythematosus susceptibility to", "systemic lupus erythematosus, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "systemic lupus erythematosus", "shortest_name_length": 3}
{"curie": "MONDO:0017699", "names": ["GSDIV, childhood combined hepatic and myopathic form", "GSD type 4, childhood combined hepatic and myopathic form", "GBE deficiency, childhood combined hepatic and myopathic form", "glycogenosis type 4, childhood combined hepatic and myopathic form", "glycogenosis type IV, childhood combined hepatic and myopathic form", "glycogen storage disease type 4, childhood combined hepatic and myopathic form", "glycogen storage disease type IV, childhood combined hepatic and myopathic form", "GSD due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form", "glycogenosis due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form", "glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form", "shortest_name_length": 52}
{"curie": "UMLS:C4055501", "names": ["Acquired Neurogenic Bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired Neurogenic Bladder", "shortest_name_length": 27}
{"curie": "MONDO:0016868", "names": ["partial deletion of chromosome 3", "partial monosomy of chromosome 3", "partial deletion of chromosome type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of chromosome 3", "shortest_name_length": 32}
{"curie": "MONDO:0016925", "names": ["partial trisomy/tetrasomy of chromosome 5", "partial trisomy/tetrasomy of chromosome type 5", "partial duplication/triplication of chromosome 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial trisomy/tetrasomy of chromosome 5", "shortest_name_length": 41}
{"curie": "UMLS:C0369168", "names": ["Epithelial Cast Formation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epithelial Cast Formation", "shortest_name_length": 25}
{"curie": "MONDO:0019716", "names": ["overgrowth syndrome", "Overgrowth syndrome", "Overgrowth Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "overgrowth syndrome", "shortest_name_length": 19}
{"curie": "UMLS:C2828013", "names": ["Stage IIA Merkel Cell Carcinoma", "Stage IIA Merkel Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Merkel Cell Carcinoma AJCC v7", "shortest_name_length": 31}
{"curie": "MONDO:0000023", "names": ["infantile liver failure", "liver failure, infantile", "infantile liver failure syndrome", "fever-associated acute infantile liver failure syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile liver failure", "shortest_name_length": 23}
{"curie": "MONDO:0700070", "names": ["POMT1 myopathy", "POMT1-related myopathy", "myopathy caused by mutation in POMT1", "myopathy caused by variation in POMT1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy caused by variation in POMT1", "shortest_name_length": 14}
{"curie": "MONDO:0007934", "names": ["RP91", "Mcdca", "BCAMD, FORMERLY", "MCDCA, FORMERLY", "Bull's eye maculopathy", "Bull's-eye maculopathy", "Maculopathy, bull's eye", "maculopathy, bull's eye", "RETINITIS PIGMENTOSA 91", "retinitis pigmentosa 91", "Chloroquine retinopathy", "Bull's eye maculopathy (finding)", "Chloroquine retinopathy (disorder)", "macular dystrophy, concentric annular", "Macular dystrophy, concentric annular", "Benign concentric annular macular dystrophy", "benign concentric annular macular dystrophy", "macular dystrophy, benign concentric annular", "MACULAR DYSTROPHY, CONCENTRIC ANNULAR, FORMERLY", "Benign concentric annular macular dystrophy (disorder)", "MACULAR DYSTROPHY, BENIGN CONCENTRIC ANNULAR, FORMERLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign concentric annular macular dystrophy", "shortest_name_length": 4}
{"curie": "MONDO:0008337", "names": ["Pterygium", "pterygium of conjunctiva and cornea", "PTERYGIUM OF CONJUNCTIVA AND CORNEA", "Pterygium of Conjunctiva and Cornea", "Pterygium Of Conjunctiva And Cornea", "familial pterygium of the conjunctiva", "pterygium of the conjunctiva and cornea"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial pterygium of the conjunctiva", "shortest_name_length": 9}
{"curie": "UMLS:C4683691", "names": ["Angioimmunoblastic T-Cell Lymphoma by Ann Arbor Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Angioimmunoblastic T-Cell Lymphoma by Ann Arbor Stage", "shortest_name_length": 53}
{"curie": "MONDO:0013462", "names": ["fucosyltransferase 6 deficiency", "FUCOSYLTRANSFERASE 6 DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fucosyltransferase 6 deficiency", "shortest_name_length": 31}
{"curie": "MONDO:0005174", "names": ["acute hypotension", "acute hypotension (disease)", "hypotension (disease), acute"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute hypotension", "shortest_name_length": 17}
{"curie": "UMLS:C0334441", "names": ["Melanoma Arising in Giant Congenital Nevus", "Malignant melanoma in giant pigmented nevus", "Malignant melanoma in giant pigmented naevus", "Malignant melanoma in congenital melanocytic nevus", "Malignant melanoma in congenital melanocytic naevus", "Malignant melanoma in giant pigmented nevus (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant melanoma in giant pigmented nevus", "shortest_name_length": 42}
{"curie": "MONDO:0017519", "names": ["symbrachydactyly of hand and foot, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "symbrachydactyly of hand and foot, unilateral", "shortest_name_length": 45}
{"curie": "MONDO:0008063", "names": ["nasal alar collapse, bilateral", "Nasal Alar Collapse, Bilateral", "NASAL ALAR COLLAPSE, BILATERAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasal alar collapse, bilateral", "shortest_name_length": 30}
{"curie": "MONDO:0003014", "names": ["Rhinitis", "RHINITIS", "rhinitis", "Rhinitides", "runny nose", "Rhinitis NOS", "Rhinitis, NOS", "Nasal Catarrh", "Nasal Catarrhs", "Catarrh, Nasal", "Catarrhs, Nasal", "nose irritation", "NOSE IRRITATION", "Nasal irritation", "NASAL IRRITATION", "nasal irritation", "irritations nose", "NASAL INFLAMMATION", "nasal inflammation", "Irritation of nose", "Nasal inflammation", "Rhinitis (disorder)", "rhinitis (diagnosis)", "Inflammation of nasal passage", "nasal cavity mucosa inflammation", "inflammation of nasal cavity mucosa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rhinitis", "shortest_name_length": 8}
{"curie": "UMLS:C5420231", "names": ["Head and Neck Histiocytic and Dendritic Cell Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Head and Neck Histiocytic and Dendritic Cell Neoplasm", "shortest_name_length": 53}
{"curie": "UMLS:C2216700", "names": ["Stage IIIC Breast Cancer", "Stage IIIC Breast Cancer AJCC v6", "Stage IIIC Breast Carcinoma AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Breast Cancer AJCC v6", "shortest_name_length": 24}
{"curie": "MONDO:0037872", "names": ["Bordetellosis", "bordetellosis", "BORDETELLOSES", "INFECT BORDETELLA", "Bordetellosis, NOS", "Bordetella infection", "Bordetella Infection", "Bordetella infections", "infection; Bordetella", "Bordetella Infections", "Infection, Bordetella", "Infections, Bordetella", "Bordetellosis (diagnosis)", "Bordetella infectious disease", "Bordetella disease or disorder", "Bordetella caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bordetellosis", "shortest_name_length": 13}
{"curie": "MONDO:0011733", "names": ["PSMNSB", "PSMNST", "parasomnia, Sleeptalking type", "PARASOMNIA, SLEEPTALKING TYPE", "parasomnia, sleep bruxism type", "PARASOMNIA, SLEEP BRUXISM TYPE", "FACIOMANDIBULAR MYOCLONUS, NOCTURNAL", "Faciomandibular myoclonus, nocturnal", "faciomandibular myoclonus, nocturnal", "nocturnal facio-mandibular myoclonus", "Nocturnal facio-mandibular myoclonus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parasomnia, sleep bruxism type", "shortest_name_length": 6}
{"curie": "UMLS:C4682588", "names": ["Stage IVA Uterine Corpus Adenosarcoma", "Stage IVA Uterine Corpus Adenosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Uterine Corpus Adenosarcoma AJCC v8", "shortest_name_length": 37}
{"curie": "UMLS:C1336226", "names": ["Stage IIIB Lung Cancer", "Stage IIIB Lung Carcinoma", "Stage IIIB Carcinoma of Lung", "Stage IIIB Lung Cancer AJCC v7", "Stage IIIB Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Lung Cancer AJCC v7", "shortest_name_length": 22}
{"curie": "UMLS:C0677954", "names": ["Stage IV Hodgkin Lymphoma", "Hodgkin's Disease Stage IV", "Stage IV Hodgkin's Disease", "Hodgkin's disease stage IV", "Stage IV Hodgkin's Lymphoma", "Hodgkin's Lymphoma Stage IV", "Hodgkin's disease NOS stage IV", "Hodgkin's disease disseminated", "Ann Arbor Stage IV Hodgkin Lymphoma", "Hodgkin's disease, unspecified site, extranodal and solid organ sites"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Hodgkin Lymphoma", "shortest_name_length": 25}
{"curie": "MONDO:0005734", "names": ["dourine", "Dourine", "Dourines", "Mal du coït", "Mal de coit", "Mal du coit", "Covering disease", "Infection by Trypanosoma equiperdum", "Infection caused by Trypanosoma equiperdum", "Infection caused by Trypanosoma equiperdum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dourine", "shortest_name_length": 7}
{"curie": "UMLS:C1336151", "names": ["Stage IC Ovarian Germ Cell Tumor", "stage IC ovarian germ cell tumor", "Stage IC Ovarian Germ Cell Tumor AJCC v7", "Stage IC Ovarian Germ Cell Tumor AJCC v6", "Stage IC Ovarian Germ Cell Tumor AJCC v6 and v7", "FIGO Stage IC Malignant Ovarian Germ Cell Tumor", "FIGO Stage IC Malignant Germ Cell Tumor of Ovary", "FIGO Stage IC Malignant Ovarian Germ Cell Neoplasm", "FIGO Stage IC Malignant Germ Cell Neoplasm of Ovary", "FIGO Stage IC Malignant Germ Cell Tumor of the Ovary", "FIGO Stage IC Malignant Germ Cell Neoplasm of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IC Ovarian Germ Cell Tumor AJCC v6 and v7", "shortest_name_length": 32}
{"curie": "MONDO:0800120", "names": ["SJS", "Mac-Leod-Swyer-James-Syndrome", "Swyer-James-(Macleod)-Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mac-Leod-Swyer-James-Syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C0855194", "names": ["Stage I Testicular Embryonal Carcinoma", "Testicular embryonal carcinoma stage I", "Stage I Testicular Embryonal Carcinoma AJCC v6", "Stage I Testicular Embryonal Carcinoma AJCC v7", "Stage I Testicular Embryonal Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular embryonal carcinoma stage I", "shortest_name_length": 38}
{"curie": "UMLS:C1334182", "names": ["Inflammatory Malignant Fibrous Histiocytoma NCI Grade 3", "Inflammatory Malignant Fibrous Histiocytoma NCI Grade III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Inflammatory Malignant Fibrous Histiocytoma NCI Grade 3", "shortest_name_length": 55}
{"curie": "MONDO:0019417", "names": ["X-linked intellectual disability-precocious puberty-obesity syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability-precocious puberty-obesity syndrome", "shortest_name_length": 68}
{"curie": "MONDO:0011856", "names": ["SmD with bowed forearms and Facial Dysmorphism", "SMD WITH BOWED FOREARMS AND FACIAL DYSMORPHISM", "SMD With Bowed Forearms And Facial Dysmorphism", "SMD with bowed forearms and facial dysmorphism", "SmD with with bowed forearms and facial dysmorphism", "Spondylometaphyseal dysplasia with bowed forearms and facial dysmorphism", "SPONDYLOMETAPHYSEAL DYSPLASIA WITH BOWED FOREARMS AND FACIAL DYSMORPHISM", "spondylometaphyseal dysplasia with bowed forearms and facial dysmorphism", "spondylometaphyseal dysplasia-bowed forearms-facial dysmorphism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondylometaphyseal dysplasia-bowed forearms-facial dysmorphism syndrome", "shortest_name_length": 46}
{"curie": "MONDO:0015418", "names": ["lateral facial cleft", "transverse facial cleft", "Tessier number 7 facial cleft"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lateral facial cleft", "shortest_name_length": 20}
{"curie": "MONDO:0018638", "names": ["Pseudohypoaldosteronism", "pseudohypoaldosteronism", "Pseudohypoaldosteronisms", "Pseudohypoadrenocorticalism", "Pseudohypoaldosteronism, NOS", "Pseudohypoaldosteronism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudohypoaldosteronism", "shortest_name_length": 23}
{"curie": "UMLS:C4551764", "names": ["stage II cervix cancer", "Cervix Cancer Stage II", "cervix cancer, stage II", "stage II cervical cancer", "Stage II Cervical Cancer", "Cervical Cancer Stage II", "cervical cancer, stage II", "AJCC Stage II Cervical Cancer", "stage II cancer of the cervix", "cancer of the cervix, stage II", "Cervix Cancer Stage II AJCC v6", "Uterine Cervix Cancer Stage II", "FIGO Stage II Cervix Carcinoma", "stage II uterine cervix cancer", "uterine cervix cancer, stage II", "Stage II Cervical Cancer AJCC v6", "AJCC Stage II Cervical Cancer v6", "Cervical Cancer Stage II AJCC v6", "FIGO Stage II Cervical Carcinoma", "uterine cervical cancer, stage II", "FIGO Stage II Carcinoma of Cervix", "Cervical Carcinoma Stage II AJCC v6", "FIGO Stage II Cervix Uteri Carcinoma", "FIGO Stage II Carcinoma of the Cervix", "FIGO Stage II Uterine Cervix Carcinoma", "Uterine Cervix Cancer Stage II AJCC v6", "FIGO Stage II Carcinoma of Cervix Uteri", "FIGO Stage II Carcinoma of Uterine Cervix", "FIGO Stage II Carcinoma of the Cervix Uteri", "FIGO Stage II Carcinoma of the Uterine Cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Cervical Cancer AJCC v6", "shortest_name_length": 22}
{"curie": "MONDO:0020323", "names": ["PMBL", "PMLCL", "Med-DLBCL", "Thymic large B-cell lymphoma", "mediastinal large B-cell lymphoma", "Mediastinal large B-cell lymphoma", "primary mediastinal B-cell lymphoma", "large cell lymphoma of the mediastinum", "Large cell lymphoma of the mediastinum", "Primary Mediastinal Large B-Cell Lymphoma", "primary mediastinal large B-cell lymphoma", "Primary mediastinal large B-cell lymphoma", "mediastinal (thymic) large B-cell lymphoma", "Mediastinal (Thymic) Large B-Cell Lymphoma", "Primary mediastinal large B-cell lymphomas", "Mediastinal (thymic) large B-cell lymphoma", "Primary mediastinal large B-cell lymphoma NOS", "Mediastinal B-Cell Diffuse Large Cell Lymphoma", "mediastinal B-cell diffuse large cell lymphoma", "B-cell diffuse large cell lymphoma of mediastinum", "B-Cell Diffuse Large Cell Lymphoma of Mediastinum", "Primary Mediastinal (Thymic) Large B-Cell Lymphoma", "Primary mediastinal (thymic) large B-cell lymphoma", "primary mediastinal (thymic) large B-cell lymphoma", "B-cell diffuse large cell lymphoma of the mediastinum", "B-Cell Diffuse Large Cell Lymphoma of the Mediastinum", "Mediastinal diffuse large-cell lymphoma with sclerosis", "mediastinal diffuse large-cell lymphoma with sclerosis", "primary mediastinal clear cell lymphoma of B-cell type", "mediastinal diffuse large cell lymphoma with sclerosis", "Primary mediastinal clear cell lymphoma of B-cell type", "Primary Mediastinal Clear Cell Lymphoma of B-Cell Type", "Mediastinal Diffuse Large Cell Lymphoma with Sclerosis", "Mediastinal large B-cell lymphoma (morphologic abnormality)", "Primary mediastinal (thymic) large B-cell lymphoma (disorder)", "primary malignant mediastinal large B-cell lymphoma of thymus", "primary malignant mediastinal large B-cell lymphoma of thymus (diagnosis)", "Large B-cell lymphoma subtype primary mediastinal (Thymic) large B-cell lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary mediastinal large B-cell lymphoma", "shortest_name_length": 4}
{"curie": "MONDO:0009638", "names": ["mitochondrial myopathy with a defect in mitochondrial-protein transport", "Mitochondrial Myopathy with a Defect in Mitochondrial Protein Transport", "MITOCHONDRIAL MYOPATHY WITH A DEFECT IN MITOCHONDRIAL-PROTEIN TRANSPORT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial myopathy with a defect in mitochondrial-protein transport", "shortest_name_length": 71}
{"curie": "MONDO:0010391", "names": ["angioma serpiginosum, X-linked", "ANGIOMA SERPIGINOSUM, X-LINKED", "Angioma serpiginosum, X-linked", "angio serpiginosum, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angioma serpiginosum, X-linked", "shortest_name_length": 30}
{"curie": "MONDO:0035313", "names": ["IgG4-related inflammatory pseudotumor of the liver", "lymphoplasmacytic inflammatory pseudotumor of the liver"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphoplasmacytic inflammatory pseudotumor of the liver", "shortest_name_length": 50}
{"curie": "MONDO:0000904", "names": ["CDCBM", "complex cortical dysplasia with other brain malformations", "cortical dysplasia, complex, with other brain malformations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complex cortical dysplasia with other brain malformations", "shortest_name_length": 5}
{"curie": "MONDO:0019707", "names": ["primary osteolysis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary osteolysis", "shortest_name_length": 18}
{"curie": "UMLS:C1260966", "names": ["Odontogenic Fibroma", "Odontogenic fibroma", "fibroma; odontogenic", "odontogenic; fibroma", "Odontogenic fibroma, NOS", "Central Odontogenic Fibroma", "Central odontogenic fibroma", "FIBROMA, ODONTOGENIC, BENIGN", "Central odontogenic epithelial hamartoma", "Central odontogenic fibroma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central odontogenic fibroma", "shortest_name_length": 19}
{"curie": "MONDO:0010072", "names": ["autosomal recessive spondyloepiphyseal dysplasia tarda", "Spondyloepiphyseal Dysplasia Tarda, Autosomal Recessive", "spondyloepiphyseal dysplasia tarda, autosomal recessive", "SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepiphyseal dysplasia tarda, autosomal recessive", "shortest_name_length": 54}
{"curie": "MONDO:0004298", "names": ["gastropathy", "GASTROPATHY", "Gastropathy", "Stomach Disease", "stomach disease", "gastric disease", "Gastric Disease", "Stomach disease", "Gastric disease", "Gastric Diseases", "Gastric disorder", "Gastric Disorder", "stomach diseases", "stomach disorder", "gastric disorder", "Stomach Diseases", "Stomach Disorder", "Disease, Stomach", "Disease, Gastric", "Stomach--Diseases", "Gastric Disorders", "Diseases, Stomach", "Stomach Disorders", "stomach disorders", "stomach; disorder", "disorder; stomach", "Diseases, Gastric", "Gastric disorders", "Disease of stomach", "disease of stomach", "disorder of stomach", "Disorder of stomach", "gastropathy (diagnosis)", "diseases of the stomach", "DISEASES OF THE STOMACH", "Disease of stomach, NOS", "stomach disease or disorder", "disease or disorder of stomach", "Disorder of stomach (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stomach disorder", "shortest_name_length": 11}
{"curie": "UMLS:C4521623", "names": ["Stage I Sinonasal Cancer AJCC v8", "Stage I Sinonasal Carcinoma AJCC v8", "Stage I Nasal Cavity and Paranasal Sinus Cancer", "Stage I Nasal Cavity and Paranasal Sinus Cancer AJCC v8", "Stage I Nasal Cavity and Paranasal Sinus Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Nasal Cavity and Paranasal Sinus Cancer AJCC v8", "shortest_name_length": 32}
{"curie": "UMLS:C0596838", "names": ["fracture limb", "Limb fracture", "Limb Fracture", "limb fracture", "Limb fractures", "fractures limb"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Limb fracture", "shortest_name_length": 13}
{"curie": "MONDO:0003435", "names": ["Microcystic adenoma", "microcystic adenoma", "Microcystic Adenoma", "Microcystic Adenomas", "Adenoma, Microcystic", "Adenomas, Microcystic", "[M] Microcystic adenoma", "Microcystic adenoma (morphologic abnormality)", "microcystic adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcystic adenoma", "shortest_name_length": 19}
{"curie": "MONDO:0010807", "names": ["DFNB2", "NSRD2", "autosomal recessive deafness 2", "DEAFNESS, AUTOSOMAL RECESSIVE 2", "Deafness, Autosomal Recessive 2", "deafness, autosomal recessive 2", "deafness, autosomal recessive type 2", "autosomal recessive nonsyndromic deafness 2", "neurosensory nonsyndromic recessive deafness 2", "NEUROSENSORY NONSYNDROMIC RECESSIVE DEAFNESS 2", "Neurosensory Nonsyndromic Recessive Deafness 2", "autosomal recessive nonsyndromic hearing loss 2", "MYO7A autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic deafness type 2", "autosomal recessive nonsyndromic deafness caused by mutation in MYO7A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 2", "shortest_name_length": 5}
{"curie": "MONDO:0005492", "names": ["hive", "Weal", "Hive", "welt", "weal", "Welt", "Welts", "welts", "hives", "WELTS", "Hives", "HIVES", "wheal", "weals", "Wheal", "hived", "Wheals", "hiving", "wheals", "WHEALS", "Wheal(s)", "URTICARIA", "Hives NOS", "urticaria", "Urticaria", "Urtication", "urticarias", "Skin wheal", "Urticarias", "urticarial", "Nettle rash", "nettle rash", "rash nettle", "rash; nettle", "nettles rash", "nettle; rash", "Urticaria NOS", "urticaria nos", "Urticated rash", "RASH URTICARIAL", "Urticarial rash", "urticarial rash", "Cutaneous wheal", "Rash urticarial", "Wheal (disorder)", "urticaria (disease)", "Urticaria (disorder)", "Unspecified urticaria", "urticaria (diagnosis)", "Urticaria, unspecified", "nettle rash (diagnosis)", "wheal (physical finding)", "Other specified urticaria", "Urticaria (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urticaria", "shortest_name_length": 4}
{"curie": "UMLS:C5418799", "names": ["Advanced Penile Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Penile Carcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0008704", "names": ["Slsd with SCID", "SLSD WITH SCID", "SLSD with SCID", "Achondroplasia-SCID syndrome", "achondroplasia-SCID syndrome", "agammaglobulinemia and achondroplasia", "Short limb skeletal dysplasia with SCID", "short limb skeletal dysplasia with SCID", "Immunodeficiency-short limb dwarfism syndrome", "immunodeficiency-short limb dwarfism syndrome", "Immunodeficiency, short limb dwarfism syndrome", "achondroplasia and Swiss-type agammaglobulinemia", "achondroplasia and Swiss type agammaglobulinemia", "achondroplasia and severe combined immunodeficiency", "achondroplasia-Swiss type agammaglobulinemia syndrome", "Achondroplasia-Swiss type agammaglobulinemia syndrome", "Achondroplasia-Swiss type agammaglobulinaemia syndrome", "achondroplasia-severe combined immunodeficiency syndrome", "Achondroplasia-severe combined immunodeficiency syndrome", "Achondroplasia, severe combined immunodeficiency syndrome", "achondroplasia so-called and severe combined immunodeficiency", "Achondroplasia, So-Called, and Severe Combined Immunodeficiency", "achondroplasia, so-called, and severe combined immunodeficiency", "ACHONDROPLASIA, SO-CALLED, AND SEVERE COMBINED IMMUNODEFICIENCY", "SHORT-LIMB SKELETAL DYSPLASIA WITH SEVERE COMBINED IMMUNODEFICIENCY", "Short-Limb Skeletal Dysplasia with Severe Combined Immunodeficiency", "short-limb skeletal dysplasia with severe combined immunodeficiency", "Short-limb skeletal dysplasia with severe combined immunodeficiency", "Short-limb skeletal dysplasia with severe combined immunodeficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short-limb skeletal dysplasia with severe combined immunodeficiency", "shortest_name_length": 14}
{"curie": "MONDO:0001087", "names": ["Schizoptypal disorder", "Schizotypal personality", "Schizotypal personality disorder", "disorder personality schizotypal", "schizotypal personality disorder", "Schizotypal Personality Disorder", "schizotypal; personality disorder", "Disorder, Schizotypal Personality", "Schizotypal Personality Disorders", "disorders personality schizotypal", "personality disorder; schizotypal", "Personality Disorder, Schizotypal", "schizotypical personality disorder", "Disorders, Schizotypal Personality", "Personality Disorders, Schizotypal", "Schizotypal personality disorder (disorder)", "schizotypal personality disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schizotypal personality disorder", "shortest_name_length": 21}
{"curie": "MONDO:0004565", "names": ["bowel; occlusion", "occlusion; bowel", "BOWEL OBSTRUCTION", "Obstruction;bowel", "Bowel obstruction", "Obstruction bowel", "Bowel Obstruction", "OBSTRUCTION BOWEL", "bowel obstruction", "obstruction bowel", "bowel; obstruction", "bowel obstructions", "obstruction; bowel", "bowels obstruction", "Intestinal blockage", "occlusion intestinal", "occlusion; intestine", "intestinal occlusion", "intestine; occlusion", "intestine obstruction", "obstruction intestine", "intestinal obstruction", "INTESTINAL OBSTRUCTION", "OBSTRUCTION INTESTINAL", "Obstruction;intestinal", "Intestinal Obstruction", "Intestinal obstruction", "Obstruction intestinal", "INTESTINE, OBSTRUCTION", "intestines obstruction", "obstruction intestinal", "Intestinal Obstructions", "Obstruction, Intestinal", "intestinal obstructions", "Obstruction of intestine", "Intestines--Obstructions", "obstruction of intestine", "Intestinal occlusion, NOS", "Intestinal obstruction NOS", "Intestinal obstruction, NOS", "IO - Intestinal obstruction", "Occlusion of intestine or colon", "Obstruction of intestine or colon", "Intestinal obstruction (disorder)", "Intestinal obstruction (diagnosis)", "Unspecified intestinal obstruction", "Occlusion of colon or intestine NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intestinal obstruction", "shortest_name_length": 16}
{"curie": "UMLS:C4330534", "names": ["Lateral Ventricle Ependymal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lateral Ventricle Ependymal Tumor", "shortest_name_length": 33}
{"curie": "MONDO:0022587", "names": ["bone dysplasia corpus callosum agenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bone dysplasia corpus callosum agenesis", "shortest_name_length": 39}
{"curie": "UMLS:C0496870", "names": ["benign liver tumor", "benign tumor liver", "benign liver tumors", "LIVER, BENIGN TUMOR", "benign liver tumour", "benign liver tumours", "benign livers tumors", "Benign tumor of liver", "benign liver neoplasm", "benign liver neoplasms", "Benign tumour of liver", "liver neoplasm, benign", "HEPATIC NEOPLASM BENIGN", "Benign hepatic neoplasm", "Hepatic neoplasm benign", "benign neoplasm of liver", "Benign neoplasm of liver", "Benign hepatic neoplasm NOS", "Benign neoplasm of liver, NOS", "Benign neoplasm of liver (disorder)", "benign neoplasm of liver (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign neoplasm of liver", "shortest_name_length": 18}
{"curie": "MONDO:0016613", "names": ["APC-related AFAP", "APC-related attenuated FAP", "APC-related attenuated familial polyposis coli", "APC-related attenuated familial adenomatous polyposis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "APC-related attenuated familial adenomatous polyposis", "shortest_name_length": 16}
{"curie": "UMLS:C4521739", "names": ["Stage I Esophageal Squamous Cell Cancer", "Pathologic Stage I Esophageal Squamous Cell Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage I Esophageal Squamous Cell Carcinoma AJCC v8", "shortest_name_length": 39}
{"curie": "UMLS:C0949091", "names": ["Candida sepsis", "candida sepsis", "sepsis; Candida"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Candida sepsis", "shortest_name_length": 14}
{"curie": "UMLS:C4329640", "names": ["CNS Solitary Fibrous Tumor", "Central Nervous System Solitary Fibrous Tumor", "CNS Solitary Fibrous Tumor/Hemangiopericytoma", "Central Nervous System Solitary Fibrous Tumor/Hemangiopericytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Solitary Fibrous Tumor", "shortest_name_length": 26}
{"curie": "UMLS:C1515129", "names": ["T-Cell Large Granular Lymphocyte Leukemia Expressing the TCR Gamma-Delta", "T-Cell Large Granular Lymphocyte Leukemia Expressing the T-Cell Receptor Gamma-Delta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-Cell Large Granular Lymphocyte Leukemia Expressing the T-Cell Receptor Gamma-Delta", "shortest_name_length": 72}
{"curie": "MONDO:0100393", "names": ["AML, t(8;16)", "acute myeloid leukemia, t(8;16)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, t(8;16)", "shortest_name_length": 12}
{"curie": "MONDO:0033555", "names": ["IMD73C", "IMMUNODEFICIENCY 73C WITH DEFECTIVE NEUTROPHIL CHEMOTAXIS AND HYPOGAMMAGLOBULINEMIA", "immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia", "shortest_name_length": 6}
{"curie": "UMLS:C0281704", "names": ["Stage III Burkitt Lymphoma", "Stage III Childhood Burkitt Lymphoma", "Stage III Childhood Burkitt's Lymphoma", "Ann Arbor Stage III Childhood Burkitt Lymphoma", "stage III childhood small noncleaved cell lymphoma", "childhood small noncleaved cell lymphoma, stage III", "stage III small noncleaved cell lymphoma, childhood", "Childhood Small Non-Cleaved Cell Lymphoma Stage III", "pediatric small noncleaved cell lymphoma, stage III", "Pediatric Small Non-Cleaved Cell Lymphoma Stage III", "Stage III Childhood Small Non-Cleaved Cell Lymphoma", "Stage III Pediatric Small Non-Cleaved Cell Lymphoma", "small noncleaved cell lymphoma, childhood, stage III", "lymphoma, stage III childhood small noncleaved cell lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Childhood Burkitt Lymphoma", "shortest_name_length": 26}
{"curie": "MONDO:0016702", "names": ["MOA", "Oligoastrocytoma", "oligoastrocytoma", "Oligoastrocytoma, NOS", "Oligoastrocytic tumor", "glioma, mixed, benign", "GLIOMA, MIXED, BENIGN", "mixed oligoastrocytoma", "Mixed oligoastrocytoma", "Mixed Oligoastrocytoma", "Mixed oligo-astrocytoma", "Oligoastrocytoma, Mixed", "mixed oligo-astrocytoma", "Mixed Oligoastrocytomas", "Mixed Oligo-Astrocytoma", "WHO Grade 2 Mixed Glioma", "WHO grade II mixed glioma", "WHO Grade II Mixed Glioma", "Mixed oligoastrocytoma (disorder)", "oligoastrocytoma; unspecified site", "Mixed Astrocytoma-Oligodendroglioma", "mixed oligodendroglioma-astrocytoma", "Mixed Oligodendroglioma Astrocytoma", "mixed astrocytoma-oligodendroglioma", "Mixed astrocytoma-oligodendroglioma", "Mixed Oligodendroglioma-Astrocytoma", "Mixed Oligodendroglioma-Astrocytomas", "Oligodendroglioma-Astrocytoma, Mixed", "Oligodendroglioma-Astrocytomas, Mixed", "mixed astrocytic-oligodendroglial tumor", "Mixed Astrocytic-Oligodendroglial Tumor", "Oligoastrocytoma, Not Otherwise Specified", "mixed astrocytic-oligodendroglial neoplasm", "Mixed Astrocytic-Oligodendroglial Neoplasm", "Mixed oligodendroglial and astrocytic tumor", "Mixed oligoastrocytoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oligoastrocytoma", "shortest_name_length": 3}
{"curie": "MONDO:0006754", "names": ["Esophageal diverticulosis", "Diverticulosis;oesophagus", "esophageal diverticulosis", "Esophageal Diverticulosis", "Diverticulosis, Esophageal", "oesophageal diverticulosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophageal diverticulosis", "shortest_name_length": 25}
{"curie": "MONDO:0005448", "names": ["hepatitis C induced liver cirrhosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatitis C induced liver cirrhosis", "shortest_name_length": 35}
{"curie": "MONDO:0008044", "names": ["DYT11", "myoclonic dystonia", "myoclonic dystonia 11", "dystonia 11, myoclonic", "dystonia-11, myoclonic", "myoclonic dystonia type 11", "myoclonus-dystonia syndrome", "alcohol-responsive dystonia", "dystonia, alcohol-responsive", "myoclonus, hereditary essential", "SGCE myoclonus-dystonia syndrome", "myoclonus-dystonia syndrome caused by mutation in SGCE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myoclonic dystonia 11", "shortest_name_length": 5}
{"curie": "MONDO:0015407", "names": ["CAMS3", "Cerebrofacial arteriovenous metameric syndrome type 3", "cerebrofacial arteriovenous metameric syndrome type 3", "Cerebrofacial arteriovenous metameric syndrome type 3 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebrofacial arteriovenous metameric syndrome type 3", "shortest_name_length": 5}
{"curie": "MONDO:0007163", "names": ["EA2", "APCA", "CAPA", "episodic ataxia type 2", "Episodic ataxia type 2", "episodic ataxia, type 2", "EPISODIC ATAXIA, TYPE 2", "Episodic Ataxia, Type 2", "familial paroxysmal ataxia", "Familial paroxysmal ataxia", "Ataxia, Familial Paroxysmal", "ataxia, familial paroxysmal", "ATAXIA, FAMILIAL PAROXYSMAL", "Ataxia, familial, paroxysmal", "Episodic ataxia type 2 (EA2)", "ataxia, familial, paroxysmal", "episodic ataxia with nystagmus", "Episodic ataxia with nystagmus", "ATAXIA, EPISODIC, WITH NYSTAGMUS", "ataxia, episodic, with Nystagmus", "Ataxia, Episodic, With Nystagmus", "Episodic ataxia type 2 (disorder)", "CACNA1A hereditary episodic ataxia", "Nystagmus-associated episodic ataxia", "Cerebellopathy, hereditary paroxysmal", "Episodic Ataxia, Nystagmus-Associated", "CEREBELLOPATHY, HEREDITARY PAROXYSMAL", "episodic ataxia, Nystagmus-associated", "EPISODIC ATAXIA, NYSTAGMUS-ASSOCIATED", "Acetazolamide-responsive episodic ataxia syndrome", "Cerebellar ataxia, paroxysmal, Acetazolamide-responsive", "CEREBELLAR ATAXIA, PAROXYSMAL, ACETAZOLAMIDE-RESPONSIVE", "cerebellar ataxia, paroxysmal, Acetazolamide-responsive", "hereditary episodic ataxia caused by mutation in CACNA1A", "Acetazolamide-responsive hereditary paroxysmal cerebellar ataxia", "ACETAZOLAMIDE-RESPONSIVE HEREDITARY PAROXYSMAL CEREBELLAR ATAXIA", "Acetazolamide-Responsive Hereditary Paroxysmal Cerebellar Ataxia", "Acetazolamide-responsive, hereditary, paroxysmal, cerebellar ataxia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "episodic ataxia type 2", "shortest_name_length": 3}
{"curie": "UMLS:C1333834", "names": ["Grade 1 Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade 1 Malignant Neoplasm", "shortest_name_length": 26}
{"curie": "UMLS:C2242796", "names": ["Microdrepanocytosis", "microdrepanocytosis", "Hemoglobin S-F disease", "Thalassemia sickle cell", "Sickle cell thalassemia", "sickle cell thalassemia", "Sickle Cell Thalassemia", "Sickle Cell-Thalassemia", "Sickle-cell thalassemia", "Haemoglobin S-F disease", "sickle cell thalassaemia", "Thalassaemia sickle cell", "HEMOGLOBIN S-THALASSEMIA", "Sickle cell thalassaemia", "hemoglobin s thalassemia", "MICRODREPANOCYTIC DISEASE", "Microdrepanocytic disease", "Sickle-cell thalassemia NOS", "SICKLE CELL THALASSEMIA DISEASE", "Sickle cell-thalassemia disease", "Sickle cell thalassemia disease", "Sickle cell thalassaemia disease", "Sickle cell-thalassaemia disease", "Thalassemia-hemoglobin S disease", "Thalassemia-haemoglobin S disease", "Sickle cell - thalassemia disease", "Thalassemia - hemoglobin S disease", "Thalassaemia-haemoglobin S disease", "sickle-cell; disorder, thalassemia", "sickle cell thalassemia (diagnosis)", "Sickle cell-thalassemia disease (disorder)", "sickle cell abnormality microdrepanocytosis", "hemoglobin disease; sickle-cell, thalassemia", "sickle-cell; hemoglobin disease, thalassemia", "disease (or disorder); sickle-cell, thalassemia", "sickle-cell; hemoglobinopathy, with thalassemia", "hemoglobinopathy; sickle-cell, with thalassemia", "sickle cell abnormality microdrepanocytosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sickle cell-thalassemia disease", "shortest_name_length": 19}
{"curie": "UMLS:C3273141", "names": ["Extrahepatic Bile Duct NET G2", "Extrahepatic Bile Duct Neuroendocrine Tumor G2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extrahepatic Bile Duct Neuroendocrine Tumor G2", "shortest_name_length": 29}
{"curie": "MONDO:0016830", "names": ["EDMD", "Emery Dreifuss Syndrome", "Emery-Dreifuss Syndrome", "Emery-Dreifuss muscular dystrophy", "Emery-Dreifuss Muscular Dystrophy", "Emery Dreifuss Muscular Dystrophy", "Muscular Dystrophy, Emery Dreifuss", "Muscular Dystrophy, Emery-Dreifuss", "muscular; dystrophy, Emery-Dreifuss", "dystrophy; muscular, Emery-Dreifuss", "Emery-Dreifuss Type Muscular Dystrophy", "Muscular Dystrophy, Emery-Dreifuss Type", "EMD - Emery-Dreifuss muscular dystrophy", "Emery-Dreifuss muscular dystrophy (disorder)", "Emery-Dreifuss muscular dystrophy (diagnosis)", "scapuloperoneal syndrome, X-linked (formerly)", "Humeroperoneal neuromuscular disease, (formerly)", "Benign scapuloperoneal muscular dystrophy with early contractures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Emery-Dreifuss muscular dystrophy", "shortest_name_length": 4}
{"curie": "MONDO:0012329", "names": ["SHORT STATURE AND FACIOAURICULOTHORACIC MALFORMATIONS", "Short Stature And Facioauriculothoracic Malformations", "short stature and Facioauriculothoracic malformations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short stature and Facioauriculothoracic malformations", "shortest_name_length": 53}
{"curie": "MONDO:0014877", "names": ["MPD5", "MYOPATHY, DISTAL, 5", "myopathy, distal, 5", "ADSSL1 distal myopathy", "myopathy, distal, type 5", "myopathy, distal, 5; MPD5", "ADSSL1-related distal myopathy", "distal myopathy caused by mutation in ADSSL1", "Adenylosuccinate synthetase-like 1-related distal myopathy", "adenylosuccinate synthetase-like 1-related distal myopathy", "Adenylosuccinate synthetase-like 1-related distal myopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy, distal, 5", "shortest_name_length": 4}
{"curie": "UMLS:C0919569", "names": ["Airway complication of anesthesia", "Airway complications of anesthesia", "Airway complication of anaesthesia", "Airway complications of anaesthesia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Airway complication of anesthesia", "shortest_name_length": 33}
{"curie": "UMLS:C4684831", "names": ["Refractory Pancreatic Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Pancreatic Carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0030917", "names": ["MRD51", "autosomal dominant mental retardation 51", "mental retardation, autosomal dominant 51", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 51", "autosomal dominant intellectual disability 51", "intellectual disability, autosomal dominant 51", "autosomal dominant intellectual developmental disorder 51", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 51"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 51", "shortest_name_length": 5}
{"curie": "MONDO:0018999", "names": ["LCAT deficiency", "lecithin-cholesterol acyltransferase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "LCAT deficiency", "shortest_name_length": 15}
{"curie": "MONDO:0013145", "names": ["BRGDA6", "Brugada Syndrome 6", "Brugada syndrome 6", "BRUGADA SYNDROME 6", "KCNE3 Brugada syndrome", "Brugada syndrome type 6", "Brugada syndrome 6 (diagnosis)", "Brugada syndrome caused by mutation in KCNE3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brugada syndrome 6", "shortest_name_length": 6}
{"curie": "MONDO:0013397", "names": ["ACNINV2", "acne inversa, familial, 2", "PSENEN familial acne inversa", "acne inversa, familial, type 2", "familial acne inversa caused by mutation in PSENEN", "ACNE INVERSA, FAMILIAL, 2, WITH OR WITHOUT DOWLING-DEGOS DISEASE", "acne inversa, familial, 2, with or without Dowling-Degos disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acne inversa, familial, 2", "shortest_name_length": 7}
{"curie": "MONDO:0016079", "names": ["sCJD", "Sporadic CJD", "sporadic CJD", "Sporadic Creutzfeldt-Jakob disease", "Sporadic Jakob-Creutzfeldt disease", "sporadic Creutzfeldt-Jakob disease", "CREUTZFELDT-JAKOB DISEASE, SPORADIC", "Creutzfeldt-Jakob Disease, Sporadic", "Sporadic Creutzfeldt-Jakob disease (disorder)", "sporadic Creutzfeldt-Jakob disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sporadic Creutzfeldt-Jakob disease", "shortest_name_length": 4}
{"curie": "UMLS:C1336165", "names": ["Stage IIA Nasopharynx Carcinoma", "Stage IIA Carcinoma of Nasopharynx", "Stage IIA Nasopharyngeal Carcinoma", "Stage IIA Carcinoma of the Nasopharynx"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Nasopharyngeal Carcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C0038586", "names": ["AODD", "AOD use disorders", "substance use disorder", "chemical use disorders", "SUBSTANCE USE DISORDER", "Substance Use Disorder", "Substance use disorder", "disorder substance use", "Substance Use Disorders", "substance use disorders", "Disorder, Substance Use", "Alcohol or Other Drug Disorder", "substance use disorders (diagnosis)", "alcohol or other drug use disorders", "alcohol and other drug use pathology", "Alcohol or Other Drugs use disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Substance Use Disorders", "shortest_name_length": 4}
{"curie": "MONDO:0025691", "names": ["DYT30", "dystonia 30", "DYSTONIA 30"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dystonia 30", "shortest_name_length": 5}
{"curie": "UMLS:C4054046", "names": ["Secondary Central Chondrosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary Central Chondrosarcoma", "shortest_name_length": 32}
{"curie": "UMLS:C5419533", "names": ["Unresectable Distal Bile Duct Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Distal Bile Duct Adenocarcinoma", "shortest_name_length": 44}
{"curie": "UMLS:C0006262", "names": ["Bronchial fistula", "Fistula bronchial", "BRONCHIAL FISTULA", "Bronchial Fistula", "bronchial fistula", "Bronchial Fistulas", "fistula; bronchial", "bronchial; fistula", "Fistula, Bronchial", "Fistulas, Bronchial", "Bronchial fistula (disorder)", "bronchial fistula (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bronchial Fistula", "shortest_name_length": 17}
{"curie": "UMLS:C4683546", "names": ["Stage I Adrenal Gland Pheochromocytoma and Sympathetic Paraganglioma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Adrenal Gland Pheochromocytoma and Sympathetic Paraganglioma AJCC v8", "shortest_name_length": 76}
{"curie": "UMLS:C0750909", "names": ["Retrograde Memory Loss", "Memory Loss, Retrograde", "Retrograde Memory Losses", "Memory Losses, Retrograde"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retrograde Memory Loss", "shortest_name_length": 22}
{"curie": "UMLS:C0858906", "names": ["pyogenic infection", "Pyogenic Infection", "infection pyogenic", "Infection pyogenic", "infections pyogenic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infection pyogenic", "shortest_name_length": 18}
{"curie": "MONDO:0012457", "names": ["IHPS2", "Pyloric Stenosis, Infantile Hypertrophic, 2", "PYLORIC STENOSIS, INFANTILE HYPERTROPHIC, 2", "pyloric stenosis, infantile hypertrophic, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyloric stenosis, infantile hypertrophic, 2", "shortest_name_length": 5}
{"curie": "UMLS:C3899345", "names": ["distal urethral cancer", "Distal Urethral Cancer", "anterior urethral cancer", "Distal Urethra Carcinoma", "Distal Urethral Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Distal Urethral Carcinoma", "shortest_name_length": 22}
{"curie": "MONDO:0033479", "names": ["SCA44", "spinocerebellar ataxia 44", "SPINOCEREBELLAR ATAXIA 44"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia 44", "shortest_name_length": 5}
{"curie": "MONDO:0011913", "names": ["AD", "AD3", "ALZHEIMER DISEASE 3", "Alzheimer disease 3", "Alzheimer's Disease 3", "Alzheimer's disease 3", "Alzheimer disease type 3", "Alzheimer disease, type 3", "Alzheimer's disease type 3", "Alzheimer disease familial 3", "ALZHEIMER DISEASE, FAMILIAL, 3", "Alzheimer Disease, Familial, 3", "Alzheimer disease, familial, 3", "Alzheimer disease 3, early onset", "Alzheimer disease 3, early-onset", "Alzheimer Disease 3, Early-Onset", "ALZHEIMER DISEASE 3, EARLY-ONSET", "Familial Alzheimer Disease, Type 3", "familial Alzheimer disease, type 3", "Alzheimer disease, familial, type 3", "Familial Alzheimer's Disease, Type 3", "familial Alzheimer's disease, type 3", "Alzheimer disease early onset type 3", "PSEN1 early-onset autosomal dominant Alzheimer disease", "Alzheimer disease, type 3, with spastic paraparesis and apraxia", "Alzheimer disease, protection against, due to APOE3-Christchurch", "Alzheimer disease, familial, 3, with spastic paraparesis and apraxia", "ALZHEIMER DISEASE, FAMILIAL, 3, WITH SPASTIC PARAPARESIS AND APRAXIA", "Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia", "Alzheimer disease, type 3, with spastic paraparesis and unusual plaques", "early-onset autosomal dominant Alzheimer disease caused by mutation in PSEN1", "Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Unusual Plaques", "ALZHEIMER DISEASE, FAMILIAL, 3, WITH SPASTIC PARAPARESIS AND UNUSUAL PLAQUES", "Alzheimer disease, familial, 3, with spastic paraparesis and unusual plaques"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alzheimer disease 3", "shortest_name_length": 2}
{"curie": "UMLS:C1334781", "names": ["Mixed Cell Type GIST", "Mixed Cell Type Gastrointestinal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mixed Cell Type Gastrointestinal Stromal Tumor", "shortest_name_length": 20}
{"curie": "UMLS:C0278517", "names": ["Recurrent NSCLC", "recurrent NSCLC", "NSCLC, recurrent", "non-oat cell lung cancer, recurrent", "recurrent nonsmall cell lung cancer", "nonsmall cell lung cancer, recurrent", "Non Small Cell Lung Cancer Recurrent", "lung cancer, non-oat cell, recurrent", "Lung cancer non-small cell recurrent", "Recurrent Non-Small Cell Lung Cancer", "Non-small cell lung cancer recurrent", "lung cancer, nonsmall cell, recurrent", "Non Small Cell Lung Cancer, Recurrent", "non-small cell lung cancer, recurrent", "Recurrent Non-Small Cell Lung Carcinoma", "Recurrent Non-Small Cell Cancer of Lung", "Recurrent Lung Non-Small Cell Carcinoma", "Recurrent Non-Small Cell Cancer of the Lung", "recurrent/relapsed non-small cell lung cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-small cell lung cancer recurrent", "shortest_name_length": 15}
{"curie": "MONDO:0016934", "names": ["Duplication of chromosome 16", "partial trisomy of chromosome 16", "Partial trisomy of chromosome 16", "Partial duplication of chromosome 16", "partial duplication of chromosome 16", "partial duplication of chromosome type 16", "Partial trisomy of chromosome 16 (disorder)", "Partial trisomy of chromosome 16 (diagnosis)", "anomaly of chromosome pair 16 partial trisomy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of chromosome 16", "shortest_name_length": 28}
{"curie": "UMLS:C1336354", "names": ["Stage IVA Mouth Verrucous Carcinoma", "Stage IVA Oral Cavity Verrucous Cancer", "Stage IVA Verrucous Carcinoma of Mouth", "Stage IVA Oral Cavity Verrucous Carcinoma", "Stage IVA Verrucous Carcinoma of the Mouth", "Stage IVA Verrucous Carcinoma of Oral Cavity", "stage IVA verrucous carcinoma of the oral cavity", "Stage IVA Verrucous Carcinoma of the Oral Cavity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Oral Cavity Verrucous Carcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C0740281", "names": ["Allergy multiple", "ALLERGY MULTIPLE", "multiple allergies", "allergies multiple", "Multiple allergies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Multiple allergies", "shortest_name_length": 16}
{"curie": "MONDO:0033569", "names": ["COXPD49", "combined oxidative phosphorylation deficiency 49", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 49"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation deficiency 49", "shortest_name_length": 7}
{"curie": "UMLS:C0235912", "names": ["Hepatorrhagia", "Liver hemorrhage", "liver hemorrhage", "hepatic bleeding", "hemorrhage liver", "Hepatic bleeding", "hemorrhage; liver", "liver; hemorrhage", "Hepatic Hemorrhage", "hepatic hemorrhage", "HEPATIC HEMORRHAGE", "Hepatic hemorrhage", "HEPATIC HAEMORRHAGE", "Hepatic haemorrhage", "Hemorrhage of liver", "Haemorrhage of liver", "hepatic hemorrhage (diagnosis)", "Hemorrhage of liver (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemorrhage of liver", "shortest_name_length": 13}
{"curie": "MONDO:0019111", "names": ["THCYT", "thrombocythemia", "Familial thrombocytosis", "familial thrombocytosis", "Familial thrombocythemia", "familial thrombocythemia", "Familial thrombocythaemia", "hereditary thrombocytosis", "Hereditary thrombocythemia", "hereditary thrombocythemia", "Hereditary thrombocythaemia", "hereditary thrombocytosis disease", "Familial thrombocytosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial thrombocytosis", "shortest_name_length": 5}
{"curie": "UMLS:C0192389", "names": ["Esophageal dilation", "dilatation esophagus", "esophagus dilatation", "esophagus; dilatation", "Esophageal dilatation", "dilatation; esophagus", "Oesophageal dilatation", "Dilatation of esophagus", "Dilatation of oesophagus", "Dilatation of esophagus (disorder)", "dilation of esophagus due to disease", "Dilation of esophagus due to disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dilation of esophagus due to disease", "shortest_name_length": 19}
{"curie": "UMLS:C1335164", "names": ["Ovarian Leydig Cell Tumor", "Leydig Cell Tumor of Ovary", "Ovarian Leydig Cell Neoplasm", "Leydig Cell Neoplasm of Ovary", "Leydig Cell Tumor of the Ovary", "Leydig Cell Neoplasm of the Ovary", "Ovarian Leydig Cell Tumor, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Leydig Cell Tumor", "shortest_name_length": 25}
{"curie": "UMLS:C5447501", "names": ["Unresectable Glioblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Glioblastoma", "shortest_name_length": 25}
{"curie": "MONDO:0032725", "names": ["DEE74", "EIEE74", "early infantile epileptic encephalopathy 74", "developmental and epileptic encephalopathy 74", "epileptic encephalopathy, early infantile, 74", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 74", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 74", "developmental and epileptic encephalopathy, 74"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 74", "shortest_name_length": 5}
{"curie": "MONDO:0012181", "names": ["SPG27", "hereditary spastic paraplegia 27", "hereditary spastic paraplegia type 27", "autosomal recessive spastic paraplegia 27", "Spastic Paraplegia 27, Autosomal Recessive", "SPASTIC PARAPLEGIA 27, AUTOSOMAL RECESSIVE", "spastic paraplegia 27, autosomal recessive", "Autosomal recessive spastic paraplegia type 27", "autosomal recessive spastic paraplegia type 27", "familial spastic paraplegia autosomal recessive type 27", "Autosomal recessive spastic paraplegia type 27 (disorder)", "Autosomal recessive spastic paraplegia type 27 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 27", "shortest_name_length": 5}
{"curie": "MONDO:0008743", "names": ["Stimmler syndrome", "Stimmler Syndrome", "STIMMLER SYNDROME", "alaninuria, microcephaly, dwarfism, enamel hypoplasia & DM syndrome", "Alaninuria with microcephaly, dwarfism, enamel hypoplasia and diabetes mellitus", "Alaninuria with Microcephaly, Dwarfism, Enamel Hypoplasia, and Diabetes Mellitus", "ALANINURIA with microcephaly, dwarfism, enamel hypoplasia, and diabetes mellitus", "ALANINURIA WITH MICROCEPHALY, DWARFISM, ENAMEL HYPOPLASIA, AND DIABETES MELLITUS", "Alaninuria, microcephaly, dwarfism, enamel hypoplasia, diabetes mellitus syndrome", "alaninuria, microcephaly, dwarfism, enamel hypoplasia & diabetes mellitus syndrome", "Alaninuria, microcephaly, dwarfism, enamel hypoplasia, diabetes mellitus syndrome (disorder)", "alaninuria, microcephaly, dwarfism, enamel hypoplasia & diabetes mellitus syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stimmler syndrome", "shortest_name_length": 17}
{"curie": "UMLS:C0340221", "names": ["trachea obstruction", "tracheal obstruction", "trachea; obstruction", "Tracheal Obstruction", "obstruction; trachea", "Tracheal obstruction", "Obstruction of trachea", "Tracheal obstruction NOS", "Tracheal obstruction, NOS", "Obstruction of trachea, NOS", "Obstructive tracheal disease", "tracheal obstruction (diagnosis)", "Obstruction of trachea (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Obstruction of trachea", "shortest_name_length": 19}
{"curie": "MONDO:0005663", "names": ["neri-barre syndrome", "Neri-Barre syndrome", "Barre Lieou Syndrome", "Barré-Liéou syndrome", "barre lieou syndrome", "Barre-Lieou syndrome", "Barre-Lieou Syndrome", "barre-lieou syndrome", "Syndrome, Barre-Lieou", "Cervicocranial Syndrome", "Syndrome of Barre-Lieou", "cervicocranial syndrome", "Syndrome of Barre Lieou", "Cervicocranial syndrome", "syndrome; cervicocranial", "cervicocranial; syndrome", "Barre-Lieou syndrome (diagnosis)", "Cervicocranial syndrome (disorder)", "cervicocranial syndrome (diagnosis)", "posterior cervical sympathetic syndrome", "Sympathetic posterior cervical syndrome", "Posterior cervical sympathetic syndrome", "Posterior Cervical Sympathetic Syndrome", "posterior cervical sympathetic; syndrome", "syndrome; posterior cervical sympathetic", "syndrome; cervical, posterior, sympathicus", "cervical; syndrome, posterior, sympathicus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Barre-Lieou syndrome", "shortest_name_length": 19}
{"curie": "MONDO:0020804", "names": ["basal cell cancer", "Basal Cell Carcinoma", "basal cell carcinoma", "epithelioma, basal cell", "Malignant basal cell tumor", "Malignant basal cell tumour", "Malignant Basal Cell Neoplasm", "malignant basal cell neoplasm", "Malignant basal cell tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "basal cell carcinoma", "shortest_name_length": 17}
{"curie": "UMLS:C5237414", "names": ["Recurrent Metastatic Skin Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Metastatic Skin Squamous Cell Carcinoma", "shortest_name_length": 49}
{"curie": "MONDO:0011095", "names": ["LVNC6", "CMD1D", "dilated cardiomyopathy 1D", "cardiomyopathy, dilated, 1D", "CARDIOMYOPATHY, DILATED, 1D", "Cardiomyopathy, Dilated, 1D", "dilated cardiomyopathy type 1D", "left ventricular noncompaction 6", "cardiomyopathy, dilated, type 1D", "LEFT VENTRICULAR NONCOMPACTION 6", "CARDIOMYOPATHY, DILATED, 1D (disorder)", "TNNT2 familial isolated dilated cardiomyopathy", "familial isolated dilated cardiomyopathy caused by mutation in TNNT2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1D", "shortest_name_length": 5}
{"curie": "MONDO:0019114", "names": ["psychogenic dystonia", "psychogenic movement disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "psychogenic movement disorders", "shortest_name_length": 20}
{"curie": "MONDO:0003081", "names": ["thalamic disease", "Thalamic Disease", "Disease, Thalamic", "Thalamic Diseases", "thalamic disorder", "Diseases, Thalamic", "dorsal plus ventral thalamus disease", "disease of dorsal plus ventral thalamus", "disorder of dorsal plus ventral thalamus", "dorsal plus ventral thalamus disease or disorder", "disease or disorder of dorsal plus ventral thalamus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thalamic disorder", "shortest_name_length": 16}
{"curie": "MONDO:0019767", "names": ["hamel cerebro-palato-cardiac syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hamel cerebro-palato-cardiac syndrome", "shortest_name_length": 37}
{"curie": "UMLS:C0748055", "names": ["PSYCHIATRIC DECOMPENSATION", "Psychiatric decompensation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Psychiatric decompensation", "shortest_name_length": 26}
{"curie": "UMLS:C0854327", "names": ["bacillus infection", "Bacillus infection", "bacillus infections", "infection; Bacillus", "Bacillus; infection", "Bacillus infection NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bacillus infection", "shortest_name_length": 18}
{"curie": "MONDO:0018004", "names": ["non-DS-AMKL", "acute megakaryoblastic leukemia without down syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute megakaryoblastic leukemia without down syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0013133", "names": ["CMM5", "melanoma, cutaneous malignant, 5", "susceptibility to cutaneous malignant melanoma 5", "melanoma, cutaneous malignant, susceptibility to, 5", "MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 5", "melanoma, cutaneous malignant, susceptibility to, type 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melanoma, cutaneous malignant, susceptibility to, 5", "shortest_name_length": 4}
{"curie": "UMLS:C4744530", "names": ["Spindle Cell Variant Thyroid Gland Papillary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spindle Cell Variant Thyroid Gland Papillary Carcinoma", "shortest_name_length": 54}
{"curie": "UMLS:C4744759", "names": ["Thyroid Gland Leiomyoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Leiomyoma", "shortest_name_length": 23}
{"curie": "UMLS:C1383860", "names": ["heart hypertrophy", "Heart Hypertrophy", "heart; hypertrophy", "hypertrophy; heart", "Hypertrophy, Heart", "Heart--Hypertrophy", "Hypertrophic;heart", "hypertrophic heart", "cardiac hypertrophy", "CARDIAC HYPERTROPHY", "Heart Hypertrophies", "Cardiac Hypertrophy", "Cardiac hypertrophy", "hypertrophy; cardiac", "Hypertrophy, Cardiac", "cardiac; hypertrophy", "Hypertrophies, Heart", "Cardiac Hypertrophies", "Hypertrophies, Cardiac"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiac Hypertrophy", "shortest_name_length": 17}
{"curie": "MONDO:0011914", "names": ["HLTS", "HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA SYNDROME", "Hypotrichosis-Lymphedema-Telangiectasia Syndrome", "hypotrichosis-lymphedema-telangiectasia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotrichosis-lymphedema-telangiectasia syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C4744727", "names": ["Locally Advanced Unresectable Cervical Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Unresectable Cervical Carcinoma", "shortest_name_length": 48}
{"curie": "MONDO:0011777", "names": ["Ad8", "AD8", "Alzheimer disease 8", "Alzheimer Disease 8", "ALZHEIMER DISEASE 8", "Alzheimer's disease 8", "Alzheimer disease type 8", "Alzheimer's disease type 8", "Alzheimer disease, familial 8", "Alzheimer Disease, Familial, 8", "Alzheimer disease, familial, 8", "ALZHEIMER DISEASE, FAMILIAL, 8", "Alzheimer's disease 8, late onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alzheimer disease 8", "shortest_name_length": 3}
{"curie": "MONDO:0010850", "names": ["OBLFC1", "oblique facial clefting 1", "facial clefting, oblique, 1", "Tessier number 4 facial cleft", "facial clefting, oblique, type 1", "oculomaxillofacial dysplasia with oblique Facial clefts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tessier number 4 facial cleft", "shortest_name_length": 6}
{"curie": "MONDO:0005750", "names": ["Stiff sickness", "ephemeral fever", "Ephemeral Fever", "ephemeral; fever", "fever; ephemeral", "Fever, Ephemeral", "Three-Day Sickness", "Three Day Sickness", "Three-day sickness", "Sickness, Three-Day", "Bovine ephemeral fever", "Bovine epizootic fever", "Ephemeral fever of cattle", "Bovine ephemeral fever (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ephemeral fever", "shortest_name_length": 14}
{"curie": "MONDO:0005506", "names": ["malignant Eccrine tumor", "Malignant Eccrine Tumor", "malignant eccrine tumor", "malignant eccrine neoplasm", "eccrine sweat gland cancer", "Malignant Eccrine Neoplasm", "Malignant Eccrine Skin Tumor", "malignant eccrine skin tumor", "cancer of eccrine sweat gland", "malignant eccrine tumor of skin", "malignant eccrine skin neoplasm", "Malignant Eccrine Tumor of Skin", "Malignant Eccrine Skin Neoplasm", "Malignant Eccrine Neoplasm of Skin", "malignant eccrine neoplasm of skin", "Malignant Eccrine Tumor of the Skin", "malignant eccrine tumor of the skin", "malignant eccrine sweat gland neoplasm", "malignant eccrine neoplasm of the skin", "Malignant Eccrine Neoplasm of the Skin", "malignant neoplasm of eccrine sweat gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eccrine sweat gland cancer", "shortest_name_length": 23}
{"curie": "UMLS:C1336752", "names": ["Thyroid Immunoblastic Lymphoma", "Immunoblastic Lymphoma of Thyroid", "Thyroid Gland Immunoblastic Lymphoma", "Immunoblastic Lymphoma of the Thyroid", "Immunoblastic Lymphoma of Thyroid Gland", "Immunoblastic Lymphoma of the Thyroid Gland", "Primary Thyroid Gland Immunoblastic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Immunoblastic Lymphoma", "shortest_name_length": 30}
{"curie": "UMLS:C5557392", "names": ["Refractory Higher Risk Myelodysplastic Syndrome", "Refractory Higher-Risk Myelodysplastic Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Higher Risk Myelodysplastic Syndrome", "shortest_name_length": 47}
{"curie": "MONDO:0007657", "names": ["giant neutrophil leukocytes", "GIANT NEUTROPHIL LEUKOCYTES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "giant neutrophil leukocytes", "shortest_name_length": 27}
{"curie": "MONDO:0013917", "names": ["NPHP15", "nephronophthisis 15", "NEPHRONOPHTHISIS 15", "nephronophthisis type 15", "CEP164 nephronophthisis (disease)", "nephronophthisis (disease) caused by mutation in CEP164"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephronophthisis 15", "shortest_name_length": 6}
{"curie": "MONDO:0043219", "names": ["MBA", "Basilar migraine", "Basilar Migraine", "basilar migraine", "basilar migraines", "basilar; migraine", "Migraine, Basilar", "migraine; basilar", "Basilar Migraines", "brainstem migraine", "Bickerstaff migraine", "basilar-type migraine", "Basilar-type Migraine", "Basilar-Type Migraine", "Basilar Type Migraine", "Bickerstaff's migraine", "Migraine, Basilar-Type", "bickerstaff's migraine", "Basilar Artery Migraine", "basilar artery migraine", "Basilar artery migraine", "Migraine, Basilar Artery", "Vertebrobasilar migraine", "vertebrobasilar migraine", "artery basilar migraines", "basilar migraine headache", "migraines vertebrobasilar", "Basilar migraine (disorder)", "migraine with brainstem aura", "basilar artery migraine with aura", "basilar migraine headache (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "migraine with brainstem aura", "shortest_name_length": 3}
{"curie": "MONDO:0024878", "names": ["Secondary carcinoma", "SECONDARY CARCINOMA", "Secondary Carcinoma", "carcinoma secondary", "secondary carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary carcinoma", "shortest_name_length": 19}
{"curie": "UMLS:C5206661", "names": ["Penile Angiosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Penile Angiosarcoma", "shortest_name_length": 19}
{"curie": "MONDO:0009832", "names": ["PAGEN1", "pancreatic agenesis", "pancreatic agenesis 1", "pancreatic agenesis type 1", "Partial pancreatic agenesis", "partial pancreatic agenesis", "Partial agenesis of pancreas", "Congenital pancreatic agenesis", "congenital pancreatic agenesis", "Agenesis of the dorsal pancreas", "Pancreatic Agenesis, Congenital", "Partial agenesis of the pancreas", "partial agenesis of the pancreas", "Pancreatic Hypoplasia, Congenital", "Partial agenesis of pancreas (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic agenesis", "shortest_name_length": 6}
{"curie": "MONDO:0017675", "names": ["punctate PPK", "Punctate PPK", "Punctate palmoplantar keratoderma", "Punctate keratosis palmoplantaris", "punctate keratosis palmoplantaris", "punctate palmoplantar keratoderma", "Keratoderma, palmoplantar punctate", "punctate palmoplantar hyperkeratosis", "Punctate palmoplantar hyperkeratosis", "hereditary palmoplantar keratoderma punctate", "Punctate palmoplantar keratoderma (disorder)", "Punctate palmoplantar keratoderma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "punctate palmoplantar keratoderma", "shortest_name_length": 12}
{"curie": "UMLS:C5446561", "names": ["Lacrimal System Mucosa-Associated Lymphoid Tissue Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lacrimal System Mucosa-Associated Lymphoid Tissue Lymphoma", "shortest_name_length": 58}
{"curie": "UMLS:C0854503", "names": ["EBV infection reactivation", "Epstein-Barr virus infection reactivation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "EBV infection reactivation", "shortest_name_length": 26}
{"curie": "MONDO:0007673", "names": ["glucoglycinuria", "GLUCOGLYCINURIA", "Glucoglycinuria", "Glucoglycinuria (finding)", "glucoglycinuria (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Glucoglycinuria", "shortest_name_length": 15}
{"curie": "MONDO:0012916", "names": ["Del(2)(p15p16.1)", "Monosomy 2p15p16.1", "monosomy 2p15p16.1", "monosomy 2p15-p16.1", "2p15p16.1 microdeletion syndrome", "2p15-p16.1 microdeletion syndrome", "chromosome 2p16.1-p15 deletion syndrome", "Chromosome 2p16.1-P15 Deletion Syndrome", "CHROMOSOME 2p16.1-p15 DELETION SYNDROME", "2p15p16.1 microdeletion syndrome (disorder)", "chromosome 2p16.1-p15 deletion syndrome, isolated cases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 2p16.1-p15 deletion syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0015350", "names": ["dup(17)(q11.2)", "Dup(17)(q11.2)", "trisomy 17q11.2", "Trisomy 17q11.2", "Grisart-Destrée syndrome", "Grisart-Destree syndrome", "Grisart Destree syndrome", "Nf1 Microduplication Syndrome", "NF1 MICRODUPLICATION SYNDROME", "NF1 Microduplication Syndrome", "17q11.2 microduplication syndrome", "17q11.2 microduplication syndrome (disorder)", "17q11.2 microduplication syndrome (diagnosis)", "chromosome 17q11.2 duplication syndrome, 1.4-mb", "CHROMOSOME 17q11.2 DUPLICATION SYNDROME, 1.4-MB", "anomaly of chromosome pair 17 partial trisomy 17q11.2 microduplication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "17q11.2 microduplication syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C4521786", "names": ["Stage II Gastric (Stomach) Cancer", "Pathologic Stage II Gastric Cancer AJCC v8", "Pathologic Stage II Gastric Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage II Gastric Cancer AJCC v8", "shortest_name_length": 33}
{"curie": "MONDO:0004339", "names": ["Tuberculum Sellae Meningioma", "tuberculum sellae meningioma", "Tuberculum sellae meningioma", "meningioma of tuberculum sellae", "Meningioma of Tuberculum Sellae", "meningioma of the Tuberculum Sellae", "Meningioma of the Tuberculum Sellae", "meningioma of the tuberculum sellae", "tuberculum sellae sella turcica neoplasm", "sella turcica neoplasm of tuberculum sellae", "meningioma of tuberculum sellae (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tuberculum sellae meningioma", "shortest_name_length": 28}
{"curie": "UMLS:C0854981", "names": ["Stage III Large Cell Lung Cancer", "Large cell lung cancer stage III", "Stage III Large Cell Lung Carcinoma", "Stage III Large Cell Carcinoma of Lung", "Stage III Large Cell Carcinoma of the Lung", "Stage III Lung Large Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Large cell lung cancer stage III", "shortest_name_length": 32}
{"curie": "MONDO:0003604", "names": ["somatotropinoma", "Somatotropinoma", "secretory pituitary tumor", "Secretory pituitary tumor", "Secretory pituitary tumour", "Functioning pituitary tumor", "functioning pituitary tumor", "Functioning pituitary tumour", "pituitary neoplasm functioning", "functioning pituitary neoplasm", "Functioning pituitary neoplasm", "hormone producing pituitary cancer", "Pituitary tumors, Hormone Producing", "pituitary tumors, hormone producing", "Functioning Pituitary Gland Neoplasm", "functioning pituitary gland neoplasm", "hormone producing pituitary neoplasm", "Hormone secreting pituitary neoplasms", "pituitary neoplasms, hormone producing", "growth hormone producing pituitary tumor", "Functioning pituitary neoplasm (disorder)", "Functioning pituitary neoplasm (diagnosis)", "pituitary gland functioning endocrine neoplasm", "functioning endocrine neoplasm of pituitary gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "functioning pituitary gland neoplasm", "shortest_name_length": 15}
{"curie": "UMLS:C0029293", "names": ["Oroantral fistula", "OROANTRAL FISTULA", "Oroantral Fistula", "Oroantral Fistulas", "Fistula, Oroantral", "fistula; oroantral", "oroantral; fistula", "Fistulas, Oroantral", "Oroantral communication", "OAF - Oroantral fistula", "OAF - oroantral fistula", "Oro-antral communication", "Oroantral fistula (disorder)", "OAC - oroantral communication", "Established oroantral fistula", "OAC - Oroantral communication", "Oroantral fistula - established", "Oroantral communication (disorder)", "Epithelialized oroantral communication", "Epithelialised oroantral communication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oroantral Fistula", "shortest_name_length": 17}
{"curie": "UMLS:C0854727", "names": ["Intracranial tumor bleeding", "Intracranial tumour bleeding", "Intracranial Tumor Hemorrhage", "Intracranial tumor hemorrhage", "Intracranial tumour haemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intracranial tumor hemorrhage", "shortest_name_length": 27}
{"curie": "MONDO:0030994", "names": ["NEDAUS", "NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISM OR SEIZURES", "neurodevelopmental disorder with or without autism or seizures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with or without autism or seizures", "shortest_name_length": 6}
{"curie": "MONDO:0030674", "names": ["TBHS2", "TEEBI HYPERTELORISM SYNDROME 2", "Teebi hypertelorism syndrome 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Teebi hypertelorism syndrome 2", "shortest_name_length": 5}
{"curie": "MONDO:0017297", "names": ["CLIPPERS", "CLIPPERS syndrome", "Chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids", "chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids", "CLIPPERS - chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids", "Chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids", "shortest_name_length": 8}
{"curie": "UMLS:C5420238", "names": ["Refractory Acute Undifferentiated Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Acute Undifferentiated Leukemia", "shortest_name_length": 42}
{"curie": "MONDO:0014862", "names": ["CPSQ3", "SPG50", "Spastic Paraplegia 50", "ADD3 spastic quadriplegia", "spastic quadriplegic cerebral palsy 3", "Cerebral Palsy, Spastic Quadriplegic 3", "CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3", "cerebral palsy, spastic quadriplegic, 3", "cerebral palsy, spastic quadriplegic, type 3", "cerebral palsy, spastic quadriplegic, 3; CPSQ3", "spastic quadriplegia caused by mutation in ADD3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral palsy, spastic quadriplegic, 3", "shortest_name_length": 5}
{"curie": "UMLS:C5667242", "names": ["Unresectable Pleomorphic Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Pleomorphic Liposarcoma", "shortest_name_length": 36}
{"curie": "MONDO:0017502", "names": ["acheiria, unilateral", "congenital absence of hand, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acheiria, unilateral", "shortest_name_length": 20}
{"curie": "UMLS:C0751743", "names": ["CNS Metabolic Disorders, Acquired", "Metabolic Disorders, CNS, Acquired", "Metabolic Disorder, Central Nervous System, Acquired"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metabolic Disorder, Central Nervous System, Acquired", "shortest_name_length": 33}
{"curie": "MONDO:0016090", "names": ["Late onset Krabbe disease", "Adult type Krabbe disease", "Krabbe disease, late-onset", "Adult-type Krabbe's disease", "late-infantile/juvenile Krabbe disease", "Late Onset Globoid Cell Leukodystrophy", "Late-Onset Globoid Cell Leukodystrophy", "Late-infantile/juvenile Krabbe disease", "Adult-type globoid cell leukodystrophy", "Globoid cell leucodystrophy late onset", "Globoid cell leucodystrophy, late-onset", "Globoid cell leukodystrophy, late-onset", "Leukodystrophy, Globoid Cell, Late-Onset", "Globoid cell leukodystrophy, late-onset (disorder)", "Galactocerebroside beta-galactosidase deficiency - late onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "late-infantile/juvenile Krabbe disease", "shortest_name_length": 25}
{"curie": "MONDO:0000640", "names": ["CPNET", "CNS PNET", "CNS Embryonal Tumor, NOS", "Central Nervous System PNET", "central nervous system PNET", "CNS embryonal tumour, NEC/NOS", "CNS primitive neuroectodermal tumor", "CNS Primitive Neuroectodermal Tumor", "central nervous system embryonal tumor", "CNS primitive neuroectodermal neoplasm", "CNS Primitive Neuroectodermal Neoplasm", "Central Primitive Neuroectodermal Tumor", "central primitive neuroectodermal tumor", "Central primitive neuroectodermal tumor", "Central primitive neuroectodermal tumour", "central primitive neuroectodermal neoplasm", "Central Primitive Neuroectodermal Neoplasm", "Central Nervous System Embryonal Tumor, NOS", "Central primitive neuroectodermal tumor, NOS", "CNS Embryonal Tumor, Not Otherwise Specified", "central nervous system neuroectodermal tumor", "central nervous system primitive neuroectodermal tumor", "Central Nervous System Primitive Neuroectodermal Tumor", "central nervous system primitive neuroectodermal neoplasm", "Central Nervous System Primitive Neuroectodermal Neoplasm", "primitive neuroectodermal tumor of central nervous system", "Central Nervous System Embryonal Tumor, Not Otherwise Specified", "Central Nervous System Primitive Neuroectodermal Tumor (WHO Grade IV)", "central nervous system primitive neuroectodermal tumor (WHO grade IV)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system primitive neuroectodermal neoplasm", "shortest_name_length": 5}
{"curie": "UMLS:C5552811", "names": ["Infantile Myofibroma", "Infantile Hemangiopericytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infantile Myofibroma", "shortest_name_length": 20}
{"curie": "MONDO:0024349", "names": ["alba pityriasis", "Pityriasis alba", "pityriasis alba", "PITYRIASIS ALBA", "Pityriasis, alba", "pityriasis; alba", "alba; pityriasis", "Pityriasis simplex", "pityriasis simplex", "simplex; pityriasis", "pityriasis; simplex", "Pityriasis streptogenes", "Pityriasis, streptogenes", "Pityriasis alba (disorder)", "pityriasis alba (diagnosis)", "Pityriasis streptogenes (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pityriasis alba", "shortest_name_length": 15}
{"curie": "MONDO:0015059", "names": ["PPA Syndrome", "PPA Syndromes", "Syndrome, PPA", "Syndromes, PPA", "non-fluent variant PPA", "Non-fluent variant PPA", "Agramatic variant of PPA", "Progressive Nonfluent Aphasia", "Aphasia, Progressive Nonfluent", "Progressive non-fluent aphasia", "Progressive Nonfluent Aphasias", "Nonfluent Aphasia, Progressive", "progressive non-fluent aphasia", "Aphasias, Progressive Nonfluent", "Nonfluent Aphasias, Progressive", "Primary Progressive Nonfluent Aphasia", "Primary Progressive Nonfluent aphasia", "Primary progressive non fluent aphasia", "Non fluent Primary Progressive Aphasia", "non-fluent primary progressive aphasia", "Non-fluent Primary Progressive Aphasia", "Agramatic variant of primary progressive aphasia", "Primary progressive non fluent aphasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive non-fluent aphasia", "shortest_name_length": 12}
{"curie": "MONDO:0002848", "names": ["Skeletal Muscle Tumor", "skeletal muscle tumor", "Tumor of Skeletal Muscle", "Skeletal Muscle Neoplasm", "tumor of Skeletal Muscle", "tumor of skeletal muscle", "skeletal muscle neoplasm", "neoplasm of skeletal muscle", "Neoplasm of Skeletal Muscle", "Neoplasm of skeletal muscle", "skeletal muscle tissue tumor", "Tumor of the Skeletal Muscle", "tumor of the skeletal muscle", "Neoplasm of the Skeletal Muscle", "neoplasm of the skeletal muscle", "tumor of skeletal muscle tissue", "skeletal muscle tissue neoplasm", "neoplasm of skeletal muscle tissue", "Neoplasm of skeletal muscle (disorder)", "neoplasm of skeletal muscle (diagnosis)", "skeletal muscle tissue neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skeletal muscle neoplasm", "shortest_name_length": 21}
{"curie": "UMLS:C2828191", "names": ["stage IV gestational trophoblastic tumor", "Stage IV Gestational Trophoblastic Tumor", "Stage IV Gestational Trophoblastic Tumor AJCC v7", "stage IV gestational trophoblastic tumor AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Gestational Trophoblastic Tumor AJCC v7", "shortest_name_length": 40}
{"curie": "MONDO:0008641", "names": ["HVR", "CRV", "RVCL", "RVCLS", "ADRVCL", "RVCL-S", "cerebroretinal vasculopathy", "grand Kaine fulling syndrome", "grand-Kaine-fulling syndrome", "hereditary vascular retinopathy", "hereditary cerebroretinal vasculopathy", "Cerebroretinal Vasculopathy, Hereditary", "CEREBRORETINAL VASCULOPATHY, HEREDITARY", "cerebroretinal vasculopathy, hereditary", "retinal vasculopathy with cerebral leukodystrophy", "vasculopathy, retinal, with cerebral leukodystrophy", "Vasculopathy, Retinal, With Cerebral Leukodystrophy", "retinal vasculopathy and cerebral leukoencephalopathy", "Retinal vasculopathy and cerebral leukoencephalopathy", "RVCL - retinal vasculopathy cerebral leukoencephalopathy", "RVCL - retinal vasculopathy cerebral leucoencephalopathy", "VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY, FORMERLY", "autosomal dominant retinal vasculopathy with cerebral leukodystrophy", "retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations", "Retinal vasculopathy with cerebral leucoencephalopathy and systemic manifestations", "Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations", "RVCL-S - retinal vasculopathy, cerebral leukoencephalopathy, systemic manifestations", "vasculopathy, retinal, with cerebral leukoencephalopathy and systemic manifestations", "VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKOENCEPHALOPATHY AND SYSTEMIC MANIFESTATIONS", "RVCL-S - retinal vasculopathy, cerebral leucoencephalopathy, systemic manifestations", "RETINOPATHY, VASCULAR, WITH CEREBRAL AND RENAL INVOLVEMENT AND RAYNAUD AND MIGRAINE PHENOMENA", "retinopathy, vascular, with cerebral and renal involvement and Raynaud and migraine phenomena", "Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations (disorder)", "Retinopathy, Vascular, With Cerebral And Renal Involvement And Raynaud And Migraine Phenomena"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations", "shortest_name_length": 3}
{"curie": "MONDO:0007980", "names": ["Fibroblast metachromasia", "metachromasia of fibroblasts", "METACHROMASIA OF FIBROBLASTS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metachromasia of fibroblasts", "shortest_name_length": 24}
{"curie": "UMLS:C1264610", "names": ["Infective peritonitis", "Infectious peritonitis", "peritonitis infectious", "Infectious peritonitis (disorder)", "Infectious peritonitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infectious peritonitis", "shortest_name_length": 21}
{"curie": "MONDO:0035293", "names": ["SP-HUS", "S. pneumoniae-associated HUS", "streptococcus pneumoniae-associated hemolytic uremic syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "streptococcus pneumoniae-associated hemolytic uremic syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C5670670", "names": ["Stage IA1 Cervical Cancer FIGO 2009", "Stage IA1 Cervical Carcinoma FIGO 2009"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA1 Cervical Cancer FIGO 2009", "shortest_name_length": 35}
{"curie": "UMLS:C4526964", "names": ["Small Intestinal, Esophageal, Colorectal, Mesenteric, and Peritoneal GIST by AJCC v8 Stage", "Small Intestinal, Esophageal, Colorectal, Mesenteric, and Peritoneal Gastrointestinal Stromal Tumor by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Intestinal, Esophageal, Colorectal, Mesenteric, and Peritoneal Gastrointestinal Stromal Tumor by AJCC v8 Stage", "shortest_name_length": 90}
{"curie": "MONDO:0004997", "names": ["CHBL", "Codman's tumor", "Chondroblastoma", "Codman's tumour", "chondroblastoma", "Chondroblastomas", "chondroblastomas", "Chondroblastoma NOS", "Chondroblastoma, NOS", "Chondroblastoma of bone", "chondroblastoma of bone", "chondroblastoma (disease)", "Chondroblastoma morphology", "Chondromatous giant cell tumor", "Chondromatous giant cell tumour", "Chondroblastoma, Not Otherwise Specified", "Chondroblastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chondroblastoma", "shortest_name_length": 4}
{"curie": "UMLS:C0280373", "names": ["oropharynx lymphoepithelioma, stage III", "Oropharyngeal lymphepithelioma stage III", "Stage III Oropharyngeal Lymphoepithelioma", "Oropharyngeal lymphoepithelioma stage III", "oropharyngeal lymphoepithelioma, stage III", "stage III lymphoepithelioma of the oropharynx", "lymphoepithelioma of the oropharynx, stage III", "Stage III Oropharyngeal Lymphoepithelioma AJCC v7", "Stage III Oropharyngeal Undifferentiated Carcinoma", "Stage III Undifferentiated Oropharyngeal Throat Cancer", "Stage III Oropharyngeal Undifferentiated Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oropharyngeal lymphoepithelioma stage III", "shortest_name_length": 39}
{"curie": "UMLS:C3272627", "names": ["Efferent Arteriolar Hyalinosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Efferent Arteriolar Hyalinosis", "shortest_name_length": 30}
{"curie": "UMLS:C0919823", "names": ["Cytolytic hepatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cytolytic hepatitis", "shortest_name_length": 19}
{"curie": "MONDO:0003280", "names": ["swayback", "Swayback", "lordosis", "LORDOSIS", "Lordosis", "Saddle back", "saddle back", "Hollow back", "hyperlordotic", "Hyperlordosis", "Lordosis, NOS", "Hyperlordotic", "human swayback", "Enzootic Ataxia", "Enzootic ataxia", "Ataxia, Enzootic", "Enzootic Ataxias", "Swayback of sheep", "Ataxias, Enzootic", "swayback of sheep", "Prominent swayback", "accentuate lordosis", "Lordosis accentuated", "Unspecified lordosis", "lordosis (diagnosis)", "Lordosis, unspecified", "deformity; saddle back", "Lordosis deformity of spine", "Swayback of sheep (disorder)", "copper deficiency myelopathy", "Lordosis accentuated (finding)", "Lordosis deformity of spine (disorder)", "Hyperlordosis deformity of lumbar spine", "Hyperlordosis deformity of lumbar spine (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "swayback", "shortest_name_length": 8}
{"curie": "MONDO:0008930", "names": ["CELIAC1", "celiac disease, susceptibility to", "CELIAC SPRUE, SUSCEPTIBILITY TO, 1", "celiac sprue, susceptibility to, 1", "susceptibility to celiac disease 1", "CELIAC DISEASE, SUSCEPTIBILITY TO, 1", "celiac disease, susceptibility to, 1", "celiac disease, susceptibility to, type 1", "gluten-sensitive enteropathy, susceptibility to, 1", "GLUTEN-SENSITIVE ENTEROPATHY, SUSCEPTIBILITY TO, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "celiac disease, susceptibility to, 1", "shortest_name_length": 7}
{"curie": "MONDO:0003715", "names": ["urachal cancer", "Urachal cancer", "urachal carcinoma", "Urachal carcinoma", "Bladder Urachal Cancer", "bladder urachal cancer", "Bladder Urachal Carcinoma", "bladder urachal carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder urachal carcinoma", "shortest_name_length": 14}
{"curie": "UMLS:C4687712", "names": ["Progressive Ependymoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Progressive Ependymoma", "shortest_name_length": 22}
{"curie": "MONDO:0008066", "names": ["nasal hyperpigmentation, familial transverse", "NASAL HYPERPIGMENTATION, FAMILIAL TRANSVERSE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasal hyperpigmentation, familial transverse", "shortest_name_length": 44}
{"curie": "UMLS:C0156253", "names": ["Renal and perinephric abscess", "Renal and Perinephric Abscess", "Renal and perinephric abscess (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal and perinephric abscess", "shortest_name_length": 29}
{"curie": "MONDO:0013874", "names": ["GCCD4", "glucocorticoid deficiency 4", "GLUCOCORTICOID DEFICIENCY 4", "glucocorticoid deficiency type 4", "NNT familial glucocorticoid deficiency", "Familial Glucocorticoid Deficiency Type 4", "familial glucocorticoid deficiency caused by mutation in NNT", "glucocorticoid deficiency 4 with or without mineralocorticoid deficiency", "GLUCOCORTICOID DEFICIENCY 4 WITH OR WITHOUT MINERALOCORTICOID DEFICIENCY", "glucocorticoid deficiency 4, with or without mineralocorticoid deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glucocorticoid deficiency 4", "shortest_name_length": 5}
{"curie": "MONDO:0000371", "names": ["mouth carcinoma in situ", "Mouth Carcinoma in situ", "Stage 0 Mouth Carcinoma", "stage 0 mouth carcinoma", "Cancer in situ of mouth", "carcinoma in situ of mouth", "Stage 0 Carcinoma of Mouth", "stage 0 oral cavity cancer", "Carcinoma in situ of mouth", "Stage 0 Oral Cavity Cancer", "Carcinoma in situ of Mouth", "stage 0 carcinoma of mouth", "oral cavity in situ carcinoma", "stage 0 oral cavity carcinoma", "Stage 0 Oral Cavity Carcinoma", "Oral Cavity Carcinoma in situ", "oral cavity carcinoma in situ", "stage 0 carcinoma of the mouth", "Stage 0 Carcinoma of the Mouth", "Carcinoma in situ of the Mouth", "carcinoma in situ of the mouth", "Carcinoma in situ of mouth, NOS", "Carcinoma in situ of Oral Cavity", "carcinoma in situ of oral cavity", "stage 0 carcinoma of oral cavity", "Stage 0 Carcinoma of Oral Cavity", "stage 0 oral cavity cancer aJCC v6", "Stage 0 Oral Cavity Cancer AJCC v6", "Stage 0 Oral Cavity Cancer AJCC v7", "stage 0 oral cavity cancer aJCC v7", "carcinoma in situ of the oral cavity", "Carcinoma in situ of the Oral Cavity", "Stage 0 Carcinoma of the Oral Cavity", "stage 0 carcinoma of the oral cavity", "Carcinoma in situ of mouth (disorder)", "Carcinoma in situ of any part of mouth", "Stage 0 Oral Cavity Cancer AJCC v6 and v7", "stage 0 oral cavity cancer aJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oral cavity carcinoma in situ", "shortest_name_length": 23}
{"curie": "MONDO:0014602", "names": ["MRD35", "autosomal dominant mental retardation 35", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 35", "mental retardation, autosomal dominant 35", "autosomal dominant intellectual disability 35", "mental retardation, autosomal dominant type 35", "intellectual disability, autosomal dominant 35", "intellectual disability, autosomal dominant type 35", "autosomal dominant intellectual developmental disorder 35", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 35", "autosomal dominant non-syndromic intellectual disability 35", "intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome", "Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome", "Intellectual disability, macrocephaly, hypotonia, behavioral abnormalities syndrome", "Intellectual disability, macrocephaly, hypotonia, behavioural abnormalities syndrome", "Intellectual disability, macrocephaly, hypotonia, behavioral abnormalities syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0007032", "names": ["PBS", "EGBRS", "Prune belly", "prune belly", "Triad Syndrome", "Triad syndrome", "triad syndrome", "Obrinsky syndrome", "Obrinsky Syndrome", "Syndrome, Obrinsky", "Obrisnksy syndrome", "prune belly syndrome", "Prune-Belly Syndrome", "Prune Belly Syndrome", "Prune belly syndrome", "prune-belly syndrome", "belly prune syndrome", "PRUNE BELLY SYNDROME", "prune belly; syndrome", "Eagle-Barret syndrome", "Prune-Belly Syndromes", "Syndrome, Prune Belly", "eagle-Barret syndrome", "Prune Belly Syndromes", "Syndrome, Prune-Belly", "syndrome; prune belly", "Eagle-Barrett syndrome", "Eagle-Barrett Syndrome", "Syndromes, Prune Belly", "Eagle Barrett syndrome", "eagle barrett syndrome", "EAGLE-BARRETT SYNDROME", "eagle-Barrett syndrome", "Syndromes, Prune-Belly", "Eagle Barrett Syndrome", "Syndrome, Eagle-Barrett", "prune belly syndrome (PBS)", "Prune belly syndrome (disorder)", "prune belly syndrome (diagnosis)", "defective abdominal wall syndrome", "aplastic abdominal muscle syndrome", "abdominal muscle syndrome; aplasia", "aplasia; abdominal muscle syndrome", "muscle deficiency syndrome; abdomen", "abdomen; muscle deficiency syndrome", "abdominal muscle deficiency anomalad", "Abdominal muscle deficiency syndrome", "abdominal muscle deficiency syndrome", "muscle; deficiency syndrome, abdomen", "Abdominal Muscle Deficiency Syndrome", "absence of abdominal muscle syndrome", "deficiency; abdominal muscle syndrome", "syndrome; abdominal muscle deficiency", "abdominal muscle syndrome; deficiency", "abdominal musculature aplasia syndrome", "syndrome; muscle deficiency, abdominal", "syndrome of agenesis of abdominal muscles", "Syndrome of Agenesis of Abdominal Muscles", "Congenital Absence of the Abdominal Muscles", "abdominal muscles, absence of, with urinary tract Abnormality and cryptorchidism", "ABDOMINAL MUSCLES, ABSENCE OF, WITH URINARY TRACT ABNORMALITY AND CRYPTORCHIDISM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prune belly syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C3897525", "names": ["Stage IIIC Rectal Cancer", "Stage IIIC Rectal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Rectal Cancer AJCC v7", "shortest_name_length": 24}
{"curie": "UMLS:C1515865", "names": ["Prostate Acinar Adenocarcinoma, Oncocytic Variant", "Acinar Prostate Adenocarcinoma, Oncocytic Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Acinar Adenocarcinoma, Oncocytic Variant", "shortest_name_length": 49}
{"curie": "MONDO:0008585", "names": ["PEE1", "PREG1", "HELLP", "hellp syndrome", "syndrome hellp", "HELLP SYNDROME", "HELLP syndrome", "HELLP Syndrome", "Syndrome, HELLP", "toxemia of pregnancy", "PREECLAMPSIA/eclampsia 1", "HELLP syndrome (diagnosis)", "hypertension, pregnancy-induced", "hemolysis, elevated liver enzymes, lowered platelets", "Hemolysis, Elevated Liver Enzymes, Lowered Platelets", "hemolysis-elevated liver enzymes-low platelets syndrome", "Hemolysis-elevated liver enzymes-low platelets syndrome", "HEMOLYSIS, ELEVATED LIVER ENZYMES, AND LOW PLATELET COUNT", "hemolysis, elevated liver enzymes, and low platelet count", "Hemolysis-Elevated Liver Enzymes-Low Platelet Count Syndrome", "hemolysis-elevated liver enzymes-low platelet count syndrome", "Hemolysis-elevated liver enzymes-low platelet count syndrome", "Hemolysis, elevated liver enzymes, low platelets in pregnancy", "hemolysis, elevated liver enzymes, low platelets in pregnancy", "Haemolysis-elevated liver enzymes-low platelet count syndrome", "Syndrome of hemolysis, elevated liver enzymes and low platelet", "Syndrome of haemolysis, elevated liver enzymes and low platelet", "HELLP syndrome (hemolysis, elevated liver enzymes, low platelets)", "HELLP (hemolysis, elevated liver enzymes, low platelets) syndrome", "HELLP - Syndrome of hemolysis, elevated liver enzymes and low platelet", "Hemolysis-elevated liver enzymes-low platelet count syndrome (disorder)", "HELLP - Syndrome of haemolysis, elevated liver enzymes and low platelet"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HELLP syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C3160815", "names": ["Intraductal papillary mucinous neoplasm", "Intraductal papillary mucinous neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraductal papillary mucinous neoplasm", "shortest_name_length": 39}
{"curie": "MONDO:0023255", "names": ["glossopalatine ankylosis micrognathia ear anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glossopalatine ankylosis micrognathia ear anomalies", "shortest_name_length": 51}
{"curie": "MONDO:0018936", "names": ["Osteoblastoma", "osteoblastoma", "Osteoblastomas", "[M]Osteoblastoma", "Osteoblastoma NOS", "Osteoblastoma, NOS", "Benign osteoblastoma", "osteoblastoma, benign", "OSTEOBLASTOMA, BENIGN", "Giant Osteoid Osteoma", "Giant osteoid osteoma", "giant osteoid osteoma", "Osteoma, Giant Osteoid", "OSTEOID OSTEOMA, GIANT", "Osteoid Osteoma, Giant", "Giant Osteoid Osteomas", "Osteoid Osteomas, Giant", "Osteomas, Giant Osteoid", "osteoblastoma (disease)", "ossifying giant cell tumor", "Ossifying Giant Cell Tumor", "FIBROMA, OSTEOGENIC, OF BONE", "Osteoblastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteoblastoma", "shortest_name_length": 13}
{"curie": "UMLS:C1262299", "names": ["Oral wart", "oral wart", "wart oral", "oral warts", "warts oral", "Oral warts", "oral papilloma", "papilloma oral", "Oral papilloma", "Oral papillomas", "Oral wart (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral wart", "shortest_name_length": 9}
{"curie": "UMLS:C5206511", "names": ["EBV LMS", "EBV-Related Leiomyosarcoma", "EBV-Associated Leiomyosarcoma", "Epstein-Barr Virus-Related Leiomyosarcoma", "Epstein-Barr Virus-Associated Leiomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "EBV-Related Leiomyosarcoma", "shortest_name_length": 7}
{"curie": "MONDO:0032803", "names": ["IMD64", "immunodeficiency 64", "IMMUNODEFICIENCY 64"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 64", "shortest_name_length": 5}
{"curie": "UMLS:C5555131", "names": ["Metastatic Low Grade Glioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Low Grade Glioma", "shortest_name_length": 27}
{"curie": "UMLS:C1334971", "names": ["Nodular Tumor", "Nodular Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nodular Neoplasm", "shortest_name_length": 13}
{"curie": "MONDO:0001417", "names": ["trachea lymphoma", "Tracheal Lymphoma", "tracheal lymphoma", "lymphoma of trachea", "Lymphoma of Trachea", "lymphoma of the trachea", "Lymphoma of the Trachea", "primary tracheal lymphoma", "Primary Tracheal Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tracheal lymphoma", "shortest_name_length": 16}
{"curie": "MONDO:0005768", "names": ["GI tuberculosis", "Tuberculosis gastrointestinal", "gastrointestinal tuberculosis", "tuberculosis gastrointestinal", "Gastrointestinal Tuberculosis", "Tuberculosis, Gastrointestinal", "Tuberculosis gastrointestinal NOS", "tuberculosis digestive tract organs", "tuberculosis of digestive tract organs", "Tuberculosis of gastrointestinal tract", "tuberculosis of gastrointestinal tract", "gastrointestinal tuberculosis (diagnosis)", "Tuberculosis of gastrointestinal tract (disorder)", "tuberculosis of digestive tract organs (diagnosis)", "Tuberculosis of intestines, peritoneum and mesenteric glands", "tuberculosis of intestines, peritoneum and mesenteric glands", "Tuberculosis of intestines, peritoneum, and mesenteric glands", "tuberculosis of intestines, peritoneum, and mesenteric glands", "Tuberculosis of intestines, peritoneum and mesenteric glands (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastrointestinal tuberculosis", "shortest_name_length": 15}
{"curie": "UMLS:C5420186", "names": ["Laryngeal Soft Tissue Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laryngeal Soft Tissue Neoplasm", "shortest_name_length": 30}
{"curie": "MONDO:0008661", "names": ["Vitiligo", "VITILIGO", "vitiligo", "Vitiligo vulgaris", "Vitiligo (disorder)", "Hypopigmentation of skin", "Blotchy loss of skin color", "Blotchy loss of skin colour", "vitiligo (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitiligo", "shortest_name_length": 8}
{"curie": "UMLS:C1096117", "names": ["Off-Label", "Off-Label Use", "off label use", "Off label use", "Off Label Use", "Off-Label Uses", "label off uses", "Off label uses", "off label uses", "Off-Label Treatment", "Unlabeled Indication", "Indication, Unlabeled", "Off-Label Prescribing", "Unlabeled Indications", "Off Label Prescribing", "Prescribing, Off-Label", "Off-Label Prescribings", "Drug use for unapproved indication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Off-Label Treatment", "shortest_name_length": 9}
{"curie": "MONDO:0006932", "names": ["Wet Lung", "Wet lung", "wet lung", "Wet Lungs", "Lung, Wet", "wet lungs", "LUNG EDEMA", "lung edema", "Edema lung", "EDEMA LUNG", "Lung edema", "Lungs, Wet", "LUNG OEDEMA", "edema; lung", "Lung oedema", "lung oedema", "lung; edema", "LUNG, EDEMA", "Oedema lung", "PULMONARY EDEMA", "Edema pulmonary", "Pulmonary edema", "Pulmonary Edema", "pulmonary edema", "EDEMA PULMONARY", "OEDEMA PULMONARY", "Oedema pulmonary", "Pulmonary Edemas", "Edema, Pulmonary", "edema, pulmonary", "Oedema;pulmonary", "Pulmonary oedema", "PULMONARY OEDEMA", "pulmonary oedema", "Edemas, Pulmonary", "Pulmonary oedemas", "Pulmonary edema NOS", "Pulmonary oedema NOS", "Pulmonary edema, NOS", "Excess fluid in lungs", "Pulmonary oedema, NOS", "Pulmonary edema (disorder)", "pulmonary edema (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary edema", "shortest_name_length": 8}
{"curie": "MONDO:0006838", "names": ["lupus", "Lupus", "Lupus exedens", "lupus exedens", "lupus vulgaris", "Lupus vulgaris", "exedens; lupus", "LUPUS VULGARIS", "Lupus Vulgaris", "lupus; exedens", "lupus; vulgaris", "vulgaris; lupus", "lupus; tuberculous", "Lupus vulgaris NOS", "lupus tuberculosis", "LV - Lupus vulgaris", "tuberculosis; lupus", "tuberculosis luposa", "Lupus - tuberculous", "lupus exedens (diagnosis)", "Tuberculosis cutis luposa", "Lupus vulgaris (disorder)", "Tuberculosis luposa cutis", "Tuberculosis lupus exedens", "lupus vulgaris (diagnosis)", "tuberculosis; lupus exedens", "tuberculosis luposa (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lupus vulgaris", "shortest_name_length": 5}
{"curie": "UMLS:C3831527", "names": ["Antepartum Obstetric Septic Embolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Antepartum Obstetric Septic Embolism", "shortest_name_length": 36}
{"curie": "MONDO:0002692", "names": ["Sinus thrombosis", "Sinus Thromboses", "sinus thrombosis", "Sinus Thrombosis", "Thromboses, Sinus", "sinus; thrombosis", "thrombosis; sinus", "Thrombosis, Sinus", "Cranial Sinus Thrombosis", "brain; thrombosis, sinus", "Cranial Sinus Thromboses", "thrombosis; brain, sinus", "Thrombosis, Cranial Sinus", "Sinus Thromboses, Cranial", "Thromboses, Cranial Sinus", "Sinus Thrombosis, Cranial", "intracranial sinus thrombosis", "Intracranial Sinus Thrombosis", "Intracranial Sinus Thromboses", "Thrombosis, Intracranial Sinus", "Sinus Thromboses, Intracranial", "Thromboses, Intracranial Sinus", "Sinus Thrombosis, Intracranial", "Venous Sinus Thrombosis, Cranial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intracranial sinus thrombosis", "shortest_name_length": 16}
{"curie": "UMLS:C4525076", "names": ["Recurrent Histiocytic and Dendritic Cell Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Histiocytic and Dendritic Cell Neoplasm", "shortest_name_length": 49}
{"curie": "UMLS:C4553704", "names": ["Stage I Fallopian Tube Cancer", "Stage I Fallopian Tube Cancer AJCC v8", "Stage I Fallopian Tube Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Fallopian Tube Cancer AJCC v8", "shortest_name_length": 29}
{"curie": "MONDO:0002398", "names": ["mucinous adenofibroma", "Mucinous Adenofibroma", "Mucinous adenofibroma", "Mucinous adenofibroma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucinous adenofibroma", "shortest_name_length": 21}
{"curie": "MONDO:0007676", "names": ["trans-stilbene oxide glutathione transferase activity", "TRANS-STILBENE OXIDE GLUTATHIONE TRANSFERASE ACTIVITY", "GLUTATHIONE TRANSFERASE ACTIVITY TOWARD TRANS-STILBENE OXIDE", "glutathione transferase activity toward trans-stilbene oxide"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glutathione transferase activity toward trans-stilbene oxide", "shortest_name_length": 53}
{"curie": "MONDO:0004907", "names": ["Bald", "bald", "BALDNESS", "ALOPECIA", "Alopecia", "baldness", "alopecia", "Baldness", "calvities", "HAIR LOSS", "Hair Loss", "Hair loss", "Alopecias", "alopecias", "hair loss", "falls hair", "Loss, Hair", "loss; hair", "hair; loss", "Hair absent", "Hair Losses", "hair falling", "loss of hair", "Falling hair", "Losses, Hair", "Loss of hair", "loss Of hair", "Alopecia NOS", "falling hair", "hair thinning", "Hair thinning", "HAIR THINNING", "thinning hair", "Alopecia, NOS", "Thinning hair", "falling hairs", "Loss (of);hair", "alopecia areata", "Alopecia Areata", "alopecia disorders", "Hair loss disorder", "Alopecia (disorder)", "alopecia (diagnosis)", "Alopecia, unspecified", "Loss of hair (finding)", "alopecia (physical finding)", "hair thinning (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alopecia", "shortest_name_length": 4}
{"curie": "MONDO:0019385", "names": ["AE", "AIE", "SREAT", "Hashimoto encephalitis", "Encephalitis autoimmune", "Autoimmune encephalitis", "Autoimmune Encephalitis", "Hashimoto's encephalitis", "Autoimmune encephalopathy", "Hashimoto's encephalopathy", "Autoimmune encephalitis, NOS", "Encephalitis allergic (autoimmune)", "Autoimmune encephalitis (disorder)", "steroid-responsive encephalopathy associated with thyroid disease", "Steroid-responsive encephalopathy associated with autoimmune thyroiditis", "steroid-responsive encephalopathy associated with autoimmune thyroiditis", "SREAT - steroid-responsive encephalopathy associated with autoimmune thyroiditis", "Steroid-responsive encephalopathy associated with autoimmune thyroiditis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "steroid-responsive encephalopathy associated with autoimmune thyroiditis", "shortest_name_length": 2}
{"curie": "MONDO:0015141", "names": ["medullar disease", "medulla oblongata disease", "disease of medulla oblongata", "disorder of medulla oblongata", "medulla oblongata disease or disorder", "disease or disorder of medulla oblongata"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of medulla oblongata", "shortest_name_length": 16}
{"curie": "MONDO:0016663", "names": ["overlapping connective tissue disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "overlapping connective tissue disease", "shortest_name_length": 37}
{"curie": "MONDO:0005798", "names": ["HIVAN", "nephropathy HIV", "HIV NEPHROPATHY", "HIV nephropathy", "HIV Nephropathy", "AIDS Nephropathy", "AIDS NEPHROPATHY", "Nephropathy, AIDS", "AIDS Nephropathies", "Nephropathies, AIDS", "HIV Related Nephropathy", "HIV-Related Nephropathy", "AIDS-related nephropathy", "Nephropathy, HIV-Related", "Nephropathy, HIV Related", "AIDS-Related Nephropathy", "HIV-Related Nephropathies", "HIV Related Nephropathies", "HIV-associated nephropathy", "hiv-associated nephropathy", "HIV Associated Nephropathy", "Nephropathies, HIV Related", "Nephropathies, HIV-Related", "HIV-associated Nephropathy", "HIV associated nephropathy", "HIV-Associated Nephropathy", "Nephropathy, HIV Associated", "AIDS Associated Nephropathy", "nephropathy aids-associated", "AIDS-Associated Nephropathy", "AIDS-associated nephropathy", "Nephropathy, HIV-Associated", "Nephropathy, AIDS Associated", "HIV Associated Nephropathies", "Nephropathy, AIDS-Associated", "HIV-Associated Nephropathies", "Nephropathies, HIV-Associated", "AIDS Associated Nephropathies", "AIDS-Associated Nephropathies", "Nephropathies, HIV Associated", "Nephropathies, AIDS Associated", "Nephropathies, AIDS-Associated", "HIV-associated nephropathy (diagnosis)", "Human immunodeficiency virus-related nephropathy", "Human Immunodeficiency Virus Associated Nephropathy", "Human Immunodeficiency Virus-Associated Nephropathy", "Acquired immune deficiency syndrome-related nephropathy", "AIDS - Acquired immune deficiency synd-related nephropathy", "Acquired immune deficiency syndrome-related nephropathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HIV-associated nephropathy", "shortest_name_length": 5}
{"curie": "UMLS:C4526735", "names": ["Lung Small Cell Carcinoma by AJCC v7 Stage", "Small Cell Lung Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Small Cell Carcinoma by AJCC v7 Stage", "shortest_name_length": 42}
{"curie": "MONDO:0000304", "names": ["penicilliosis", "infection due to Penicillium marneffei", "Infection due to Talaromyces marneffei", "Penicillium marneffei infectious disease", "Talaromyces marneffei infectious disease", "infection caused by Talaromyces marneffei", "Infection caused by Penicillium marneffei", "Talaromyces marneffei disease or disorder", "infection caused by Penicillium marneffei", "Infection caused by Talaromyces marneffei", "Talaromyces marneffei caused disease or disorder", "Infection due to Penicillium marneffei (disorder)", "Infection caused by Talaromyces marneffei (disorder)", "Disseminated infection caused by Penicillium marneffei", "Disseminated infection caused by Talaromyces marneffei", "Disseminated infection caused by Talaromyces marneffei (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "penicilliosis", "shortest_name_length": 13}
{"curie": "MONDO:0001322", "names": ["pericardial tumor", "Pericardial tumor", "pericardium cancer", "PERICARDIAL CANCER", "cancer of pericardium", "Malignant Pericardial Tumor", "malignant pericardial tumor", "Malignant Tumor of Pericardium", "malignant pericardium neoplasm", "malignant pericardial neoplasm", "Malignant Pericardial Neoplasm", "malignant tumor of Pericardium", "Malignant pericardial neoplasm", "malignant tumor of pericardium", "Malignant Neoplasm of Pericardium", "malignant neoplasm of pericardium", "Malignant neoplasm of pericardium", "Malignant Tumor of the Pericardium", "malignant tumor of the pericardium", "malignant neoplasm of the pericardium", "Malignant Neoplasm of the Pericardium", "primary malignant pericardial neoplasm", "Primary malignant neoplasm of pericardium", "malignant pericardial neoplasm (diagnosis)", "malignant cardiac neoplasm pericardial primary", "primary malignant pericardial neoplasm (diagnosis)", "Primary malignant neoplasm of pericardium (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pericardium cancer", "shortest_name_length": 17}
{"curie": "MONDO:0019638", "names": ["renal dysplasia", "renal dysplasia (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal dysplasia", "shortest_name_length": 15}
{"curie": "MONDO:0018305", "names": ["cgd", "CGD", "Quie syndrome", "Bridges-Good syndrome", "Congenital dysphagocytosis", "congenital dysphagocytosis", "dysphagocytosis; congenital", "Chronic septic granulomatosis", "granulomatous chronic disease", "chronic septic granulomatosis", "chronic disease granulomatous", "chronic granulomatous disease", "CHRONIC GRANULOMATOUS DISEASE", "Chronic Granulomatous Disease", "Chronic granulomatous disease", "Chronic Granulomatous Diseases", "Granulomatous Disease, Chronic", "granulomatous disease, chronic", "CHRONIC GRANULOMATOUS DISEASES", "Granulomatous Diseases, Chronic", "Chronic granulomatous disease, NOS", "CGD - Chronic granulomatous disease", "congenital dysphagocytosis (diagnosis)", "Chronic granulomatous disease (disorder)", "chronic granulomatous disease (diagnosis)", "Chronic granulomatous disease (CGD) of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic granulomatous disease", "shortest_name_length": 3}
{"curie": "MONDO:0005010", "names": ["cad", "CHD", "CAD", "ashd", "ASHD", "coronary disease", "Coronary Disease", "cardiac ischemia", "Coronary disease", "CORONARY DISEASE", "Coronary atheroma", "Cardiac sclerosis", "Disease, Coronary", "Coronary Diseases", "cardiac ischaemia", "coronary diseases", "coronary disorder", "coronary atheroma", "Coronary Disorders", "Coronary sclerosis", "CORONARY SCLEROSIS", "sclerosis; cardiac", "coronary sclerosis", "Diseases, Coronary", "cardiac; sclerosis", "myocardial ischemia", "coronary; sclerosis", "sclerosis; coronary", "myocardial ischaemia", "Coronary Heart Disease", "Coronary heart disease", "coronary heart disease", "Disease coronary artery", "DISEASE CORONARY ARTERY", "ischaemic heart disease", "Coronary artery disease", "Coronary Artery Disease", "coronary artery disease", "Heart Disease, Coronary", "Coronary Heart Diseases", "arteriosclerosis; heart", "heart; arteriosclerosis", "coronary heart diseases", "Disease, Coronary Heart", "CORONARY ARTERY DISEASE", "coronary artery diseases", "Artery Disease, Coronary", "Coronary Artery Diseases", "Heart Diseases, Coronary", "DISORDER CORONARY ARTERY", "Disorder coronary artery", "Coronary Atherosclerosis", "heart; disease, coronary", "CORONARY ARTERY DISEASES", "Coronary atherosclerosis", "coronary artery disorder", "CORONARY ARTERY DISORDER", "Coronary Atheroscleroses", "Diseases, Coronary Heart", "Coronary artery disorder", "coronary atherosclerosis", "CORONARY ATHEROSCLEROSIS", "coronary arteriosclerosis", "Coronary arteriosclerosis", "CORONARY ARTERIOSCLEROSIS", "Coronary Arterioscleroses", "Coronary Arteriosclerosis", "Atheroscleroses, Coronary", "Coronary (artery) disease", "Coronary artery disorders", "Coronary artery sclerosis", "Artery Diseases, Coronary", "Atherosclerosis, Coronary", "disease of coronary artery", "arteriosclerosis; coronary", "coronary; arteriosclerosis", "Arterioscleroses, Coronary", "artery; disorder, coronary", "Arteriosclerosis, Coronary", "coronary (artery); disease", "Disorder of coronary artery", "Coronary (artery) sclerosis", "disorder of coronary artery", "chronic myocardial ischemia", "Chronic myocardial ischemia", "Coronary artery disease NOS", "CHD - Coronary heart disease", "Coronary artery disease, NOS", "Ischaemia;myocardial;chronic", "Chronic myocardial ischaemia", "CHD (coronary heart disease)", "chronic myocardial ischaemia", "Atherosclerotic heart disease", "Disease;ischaem heart;chronic", "CAD - Coronary artery disease", "Disease;atherosclerotic;heart", "CAD (coronary artery disease)", "atherosclerotic heart disease", "disorder of coronary arteries", "ATHEROSCLEROTIC HEART DISEASE", "ischemic heart disease chronic", "Coronary artery disorder (NOS)", "Chronic coronary insufficiency", "chronic coronary insufficiency", "ARTERIOSCLEROTIC HEART DISEASE", "Arteriosclerotic heart disease", "arteriosclerotic heart disease", "chronic ischemic heart disease", "CORONARY ARTERY DISORDER (NOS)", "Chronic ischemic heart disease", "atherosclerosis coronary artery", "chronic ischaemic heart disease", "coronary artery atherosclerosis", "Chronic ischaemic heart disease", "Coronary artery atherosclerosis", "Arteriosclerosis coronary artery", "ARTERIOSCLEROSIS CORONARY ARTERY", "Coronary artery arteriosclerosis", "Coronary (artery) atherosclerosis", "Atherosclerotic heart disease NOS", "Atherosclerosis of coronary artery", "atherosclerosis of coronary artery", "coronary artery disease (diagnosis)", "coronary artery disease or disorder", "arteriosclerosis; coronary (artery)", "Coronary arteriosclerosis (disorder)", "Ischemic heart disease (chronic) NOS", "coronary arteriosclerosis (diagnosis)", "Chronic myocardial ischemia (disorder)", "CORONARY ATHEROSCLEROTIC HEART DISEASE", "disease or disorder of coronary artery", "Disorder of coronary artery (disorder)", "chronic myocardial ischemia (diagnosis)", "disease (or disorder); artery, coronary", "Arteriosclerotic coronary artery disease", "disease (or disorder); coronary (artery)", "ATHEROSCLEROTIC CORONARY VASCULAR DISEASE", "Chronic ischemic heart disease (disorder)", "disorder of coronary arteries (diagnosis)", "Atherosclerosis of native coronary artery", "chronic ischemic heart disease (diagnosis)", "Ischemic heart disease or syndrome, chronic", "Chronic ischemic heart disease, unspecified", "Chronic ischaemic heart disease, unspecified", "Atherosclerosis of coronary artery (disorder)", "atherosclerosis of coronary artery (diagnosis)", "disease (or disorder); heart, artery, arterial", "disease (or disorder); arteriosclerotic, heart", "Plaque build-up in arteries supplying blood to heart", "disease (or disorder); arteriosclerotic, coronary (artery)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coronary artery disorder", "shortest_name_length": 3}
{"curie": "UMLS:C0025945", "names": ["Diabetic Microangiopathy", "Diabetic microangiopathy", "Microangiopathy, Diabetic", "Diabetic Microangiopathies", "Microangiopathies, Diabetic", "Small vessel disease of diabetes mellitus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Microangiopathy, Diabetic", "shortest_name_length": 24}
{"curie": "UMLS:C2981366", "names": ["Cancer Stage (Antiquated)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cancer Stage (Antiquated)", "shortest_name_length": 25}
{"curie": "OMIM:607174", "names": ["MENINGIOMA, FAMILIAL, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 39}
{"curie": "UMLS:C5205704", "names": ["Sinonasal Adenocarcinoma, Intestinal-Type with Colonic Pattern"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Adenocarcinoma, Intestinal-Type with Colonic Pattern", "shortest_name_length": 62}
{"curie": "MONDO:0034022", "names": ["BTHLM2", "EDSMYP", "myopathic EDS", "Bethlem myopathy 2", "BETHLEM MYOPATHY 2", "EDS, myopathic type", "EDS, MYOPATHIC TYPE", "Bethlem myopathy type 2", "COL12A1 Bethlem myopathy", "myopathic Ehlers-Danlos syndrome", "Ehlers-Danlos syndrome, myopathic type", "EHLERS-DANLOS SYNDROME, MYOPATHIC TYPE", "Bethlem myopathy caused by mutation in COL12A1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bethlem myopathy 2", "shortest_name_length": 6}
{"curie": "UMLS:C1266017", "names": ["Malignant Enteroglucagonoma", "malignant enteroglucagonoma", "malignant enteroglucagonoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant enteroglucagonoma", "shortest_name_length": 27}
{"curie": "UMLS:C5557398", "names": ["Vulvar Epithelioid Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Epithelioid Sarcoma", "shortest_name_length": 26}
{"curie": "UMLS:C0334282", "names": ["Malignant glucagonoma", "Malignant Glucagonoma", "Glucagonoma, malignant", "Malignant alpha cell tumor", "Alpha-cell tumor, malignant", "Alpha cell tumor, malignant", "Malignant alpha cell tumour", "Alpha cell tumour, malignant", "glucagon producing carcinoma", "glucagon secreting carcinoma", "carcinoma, glucagon producing", "carcinoma, glucagon secreting", "Pancreatic Alpha Cell Carcinoma", "pancreas; malignant glucagonoma", "pancreatic alpha cell carcinoma", "pancreas; glucagonoma, malignant", "malignant pancreatic glucagonoma", "Malignant Pancreatic Glucagonoma", "glucagonoma; malignant, pancreas", "malignant; glucagonoma, pancreas", "carcinoma, pancreatic alpha cell", "carcinoma, alpha cell, pancreatic", "Malignant glucagonoma of pancreas", "malignant glucagonoma of pancreas", "pancreas; alpha cell tumor, malignant", "alpha cell; tumor, malignant, pancreas", "tumor; alpha cell, malignant, pancreas", "pancreas; tumor, alpha cell, malignant", "glucagonoma; malignant, unspecified site", "malignant; glucagonoma, unspecified site", "Malignant alpha cell neoplasm of pancreas", "Malignant glucagonoma of pancreas (disorder)", "malignant glucagonoma of pancreas (diagnosis)", "tumor; alpha cell, malignant, unspecified site", "alpha cell; tumor, malignant, unspecified site", "Glucagonoma, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Glucagonoma, malignant", "shortest_name_length": 21}
{"curie": "UMLS:C0342117", "names": ["colloid nodule", "Colloid nodule", "Colloid Nodule", "colloid nodules", "Thyroid colloid nodule", "thyroid colloid nodule", "colloid thyroid nodule", "thyroid nodule colloid", "Thyroid colloid nodule (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid colloid nodule", "shortest_name_length": 14}
{"curie": "MONDO:0003390", "names": ["glycogen-rich carcinoma", "Breast Glycogen-Rich Carcinoma", "glycogen-rich carcinoma of breast", "glycogen-rich clear cell breast carcinoma", "glycogen-rich, clear cell breast carcinoma", "Glycogen-Rich, Clear Cell Breast Carcinoma", "Breast Glycogen-Rich, Clear Cell Carcinoma", "glycogen-rich carcinoma of breast (diagnosis)", "glycogen-rich carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen-rich clear cell breast carcinoma", "shortest_name_length": 23}
{"curie": "MONDO:0019730", "names": ["LCDD", "chain disease light", "Bence Jones Myeloma", "Light Chain Disease", "Light chain disease", "LIGHT CHAIN DISEASE", "Bence Jones myeloma", "light chain disease", "chain disease lights", "chains disease light", "Light Chain Gammopathy", "Light chain gammopathy", "Light chain disease, NOS", "light chain deposition disease", "Light Chain Deposition Disease", "Light-chain deposition disease", "Light chain disease (disorder)", "Light chain deposition disease", "Light chain deposition disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "light chain deposition disease", "shortest_name_length": 4}
{"curie": "MONDO:0015388", "names": ["Polyrhinia", "Polyrrhinia", "Double nose", "polyrrhinia", "Congenital duplication of nose", "Congenital duplication of nose (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyrrhinia", "shortest_name_length": 10}
{"curie": "MONDO:0010617", "names": ["Sohval Soffer syndrome", "Sohval-Soffer syndrome", "Congenital testicular deficiency", "hypogonadism, MALE, with mental retardation and skeletal anomalies", "HYPOGONADISM, MALE, WITH MENTAL RETARDATION AND SKELETAL ANOMALIES", "Hypogonadism, Male, With Mental Retardation And Skeletal Anomalies", "hypogonadism, MALE, with intellectual disability and skeletal anomalies", "male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome", "Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome", "Male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome", "male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome", "Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder)", "male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome", "shortest_name_length": 22}
{"curie": "MONDO:0009464", "names": ["INTERLEUKIN 1, DEFECTIVE T-CELL RESPONSE TO", "Interleukin 1, defective T-cell response to", "IMMUNODEFICIENCY WITH DEFECTIVE T-CELL RESPONSE TO INTERLEUKIN 1", "immunodeficiency with defective T-cell response to interleukin 1", "immunodeficiency with defective T-cell response to Interleukin type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency with defective T-cell response to interleukin 1", "shortest_name_length": 43}
{"curie": "MONDO:0015818", "names": ["aggressive primary cutaneous B-cell lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aggressive primary cutaneous B-cell lymphoma", "shortest_name_length": 44}
{"curie": "UMLS:C1332162", "names": ["Acute Thymic Involution"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Thymic Involution", "shortest_name_length": 23}
{"curie": "MONDO:0012075", "names": ["ODCRCS", "oligodontia-colorectal cancer syndrome", "OLIGODONTIA-COLORECTAL CANCER SYNDROME", "Oligodontia-Colorectal Cancer Syndrome", "Tooth Agenesis-Colorectal Cancer Syndrome", "tooth agenesis-colorectal cancer syndrome", "TOOTH AGENESIS-COLORECTAL CANCER SYNDROME", "oligodontia-cancer predisposition syndrome", "autosomal dominant ectodermal dysplasia-cancer predisposition syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oligodontia-cancer predisposition syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0004569", "names": ["brachial plexus lesion", "Lesion;brachial plexus", "BRACHIAL PLEXUS LESION", "Brachial plexus lesion", "brachial plexus lesions", "lesion; brachial plexus", "brachial plexus; lesion", "Brachial plexus lesions", "plexus brachialis; lesion", "lesion of brachial plexus", "Brachial plexus lesion, NOS", "brachial plexus neuropathy from injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachial plexus neuropathy from injury", "shortest_name_length": 22}
{"curie": "UMLS:C0596763", "names": ["Immunotoxicity", "immunotoxicity", "TOXICITY_IMMUNE", "toxic reaction in immunology"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immunotoxicity", "shortest_name_length": 14}
{"curie": "MONDO:0016244", "names": ["aHUS", "D-HUS", "Non Stx Hus", "Non-Stx-Hus", "Atypical HUS", "atypical HUS", "HUS, atypical", "Nonenteropathic HUS", "HUS, Nonenteropathic", "Nonenteropathic HUSs", "HUSs, Nonenteropathic", "Atypical hemolytic uremic syndrome", "Atypical Hemolytic-Uremic Syndrome", "Atypical Hemolytic Uremic Syndrome", "atypical hemolytic-uremic syndrome", "Atypical hemolytic-uremic syndrome", "atypical hemolytic uremic syndrome", "Hemolytic Uremic Syndrome, Atypical", "Hemolytic-Uremic Syndrome, Atypical", "Atypical Hemolytic-Uremic Syndromes", "Syndrome, Atypical Hemolytic-Uremic", "Non Shiga Like Toxin Associated HUS", "Non-Shiga-Like Toxin-Associated HUS", "Atypical haemolytic uraemic syndrome", "Hemolytic-Uremic Syndromes, Atypical", "Syndromes, Atypical Hemolytic-Uremic", "Non-Shiga-Like Toxin-Associated HUSs", "HUS, Non-Shiga-Like Toxin-Associated", "Toxin-Associated HUS, Non-Shiga-Like", "Toxin-Associated HUSs, Non-Shiga-Like", "HUSs, Non-Shiga-Like Toxin-Associated", "D-minus hemolytic uremic syndrome (D-HUS)", "aHUS - atypical hemolytic uremic syndrome", "hemolytic-uremic syndrome without diarrhea", "aHUS - atypical haemolytic uraemic syndrome", "Atypical hemolytic uremic syndrome (disorder)", "Non-diarrhea-associated Hemolytic Uremic Syndrome", "non-diarrhea-associated hemolytic uremic syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical hemolytic-uremic syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0010032", "names": ["cornea scratch", "Corneal scratch", "corneal abrasion", "Corneal Abrasion", "Corneal abrasion", "cornea; abrasion", "abrasion; cornea", "abrasion corneal", "Abrasion;corneal", "cornea scratched", "CORNEAL ABRASION", "Corneal abrasions", "abrasions corneal", "Scratch to cornea", "corneas scratched", "Scratch of cornea", "Corneal Abrasions", "Abrasion, Corneal", "abrasion of cornea", "CA - Corneal abrasion", "cornea; injury, abrasion", "injury; cornea, abrasion", "INJURY, CORNEA, ABRASION", "Corneal abrasion (disorder)", "abrasion of cornea (diagnosis)", "corneal abrasion (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Corneal Abrasions", "shortest_name_length": 14}
{"curie": "UMLS:C1882066", "names": ["Nervous System Neoplasm (Antiquated)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nervous System Neoplasm (Antiquated)", "shortest_name_length": 36}
{"curie": "MONDO:0018076", "names": ["TB", "tb", "TBC", "tbc", "Tuberculous", "tuberculous", "TUBERCULOSIS", "Tuberculoses", "tuberculosis", "Tuberculotic", "Koch Disease", "Tuberculosis", "INFECTION TBC", "Infection TBC", "Kochs disease", "Kochs Disease", "Koch's Disease", "Koch; infection", "infection; Koch", "Tuberculosis NOS", "tuberculosis (TB)", "Tuberculosis (TB)", "Tuberculosis, NOS", "TB - Tuberculosis", "TB (tuberculosis)", "Active Tuberculosis", "tuberculosis active", "Active tuberculosis", "active tuberculosis", "TUBERCULOSIS ACTIVE", "tuberculosis disease", "Tuberculosis, active", "Tuberculosis Disease", "tuberculosis; general", "INFECTION TUBERCULOSIS", "infection tuberculosis", "infection; tuberculous", "Infection tuberculosis", "Tuberculous infections", "Tuberculosis (A15-A19)", "tuberculosis infection", "Tuberculosis (disorder)", "tuberculosis; infection", "tuberculosis (diagnosis)", "Tuberculous (qualifier value)", "Active tuberculosis (disorder)", "Active tuberculosis (diagnosis)", "Mycobacterium tuberculosis infection", "Mycobacterium tuberculosis Infection", "Infection, Mycobacterium tuberculosis", "Mycobacterium tuberculosis Infections", "Infections, Mycobacterium tuberculosis", "MTB - Mycobacterium tuberculosis infection", "Infection due to Mycobacterium tuberculosis", "Infection caused by Mycobacterium tuberculosis", "Infection caused by Mycobacterium tuberculosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tuberculosis", "shortest_name_length": 2}
{"curie": "UMLS:C1168241", "names": ["Eye muscle weakness", "Eye Muscle Weakness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eye muscle weakness", "shortest_name_length": 19}
{"curie": "MONDO:0009305", "names": ["IMD59", "immunodeficiency 59", "immunodeficiency 59 and hypoglycemia", "IMMUNODEFICIENCY 59 AND HYPOGLYCEMIA", "granulocytopenia with immunoglobin abnormality", "granulocytopenia with immunoglobulin abnormality", "GRANULOCYTOPENIA WITH IMMUNOGLOBULIN ABNORMALITY", "Granulocytopenia with Immunoglobulin Abnormality"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "granulocytopenia with immunoglobulin abnormality", "shortest_name_length": 5}
{"curie": "UMLS:C5417733", "names": ["VSAA", "Very Severe Aplastic Anemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Very Severe Aplastic Anemia", "shortest_name_length": 4}
{"curie": "MONDO:0000490", "names": ["Glomeruloscleroses", "GLOMERULOSCLEROSIS", "Glomerulosclerosis", "glomerulosclerosis", "glomerular sclerosis", "Glomerular Sclerosis", "Glomerular sclerosis", "Glomerulosclerosis NOS", "Glomerulosclerosis, NOS", "Renal glomerular fibrosis", "Glomerulosclerosis (disorder)", "glomerulosclerosis (diagnosis)", "Glomerulosclerosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glomerulosclerosis", "shortest_name_length": 18}
{"curie": "MONDO:0013073", "names": ["FNEPPK", "Ppkfne", "PPKFNE", "FNEPPK1", "Focal PPK", "Familial tylosis", "Late onset tylosis (type A)", "Early onset tylosis (type B)", "Focal palmoplantar keratoderma", "Focal Palmoplantar Keratoderma", "Focal keratosis palmoplantaris", "Palmoplantar keratoderma, focal", "PALMOPLANTAR KERATODERMA, FOCAL", "Focal palmoplantar hyperkeratosis", "KRT16 nonepidermolytic palmoplantar keratoderma", "Focal Nonepidermolytic Palmoplantar Keratoderma", "focal nonepidermolytic palmoplantar keratoderma", "FOCAL NONEPIDERMOLYTIC PALMOPLANTAR KERATODERMA", "Keratoderma, Focal Nonepidermolytic Palmoplantar", "Focal non epidermolytic palmoplantar keratoderma", "KERATODERMA, FOCAL NONEPIDERMOLYTIC PALMOPLANTAR", "keratoderma, focal nonepidermolytic palmoplantar", "Focal Non-Epidermolytic Palmoplantar Keratoderma", "palmoplantar keratoderma, nonepidermolytic, focal", "Palmoplantar Keratoderma, Nonepidermolytic, Focal", "focal nonepidermolytic palmoplantar keratoderma 1", "palmoplantar keratoderma, nonepidermolytic, focal 1", "PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL 1", "palmoplantar keratoderma, nonepidermolytic, focal type 1", "Hyperkeratosis of the palms and soles and esophageal papillomas", "nonepidermolytic palmoplantar keratoderma caused by mutation in KRT16"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "palmoplantar keratoderma, nonepidermolytic, focal 1", "shortest_name_length": 6}
{"curie": "MONDO:0003940", "names": ["Kümmell disease", "Kummell disease", "Vertebral trauma", "kummell's disease", "Kummell's disease", "Kümmell; spondylitis", "spondylitis; Kümmell", "Kummell's spondylitis", "Kümmell's spondylitis", "Traumatic spondylopathy", "Spondylopathy traumatic", "traumatic spondylopathy", "Kummell-Verneuil disease", "traumatic; spondylopathy", "Kümmell-Verneuil disease", "spondylopathy; traumatic", "Posttraumatic spondylitis", "Kümmell disease (disorder)", "Kummell's disease or spondylitis", "Traumatic spondylopathy (disorder)", "traumatic spondylopathy (diagnosis)", "bony vertebral centrum osteonecrosis", "avascular necrosis of a vertebral body", "osteonecrosis of bony vertebral centrum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kummell disease", "shortest_name_length": 15}
{"curie": "MONDO:0007169", "names": ["ALP", "ATHS", "ATHEROSCLEROSIS SUSCEPTIBILITY", "atherosclerosis susceptibility", "ATHEROGENIC LIPOPROTEIN PHENOTYPE", "Atherogenic lipoprotein phenotype", "atherosclerosis, susceptibility to", "Atherogenic lipoprotein phenotype (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atherosclerosis susceptibility", "shortest_name_length": 3}
{"curie": "MONDO:0014187", "names": ["AAT8", "AORTIC ANEURYSM, FAMILIAL THORACIC 8", "aortic aneurysm, familial thoracic 8", "aortic aneurysm, familial thoracic type 8", "PRKG1 familial thoracic aortic aneurysm and aortic dissection", "familial thoracic aortic aneurysm and aortic dissection caused by mutation in PRKG1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic aneurysm, familial thoracic 8", "shortest_name_length": 4}
{"curie": "UMLS:C1332165", "names": ["Adenocarcinoma and Small Cell Lung Carcinoma", "Adenocarcinoma and Small Cell Carcinoma of Lung", "Adenocarcinoma and Small Cell Carcinoma of the Lung", "Combined Small Cell Lung Carcinoma and Lung Adenocarcinoma", "Combined Lung Small Cell Carcinoma and Lung Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Combined Lung Small Cell Carcinoma and Lung Adenocarcinoma", "shortest_name_length": 44}
{"curie": "UMLS:C0278579", "names": ["recurrent cervix cancer", "cervix cancer recurrent", "recurrent cervical cancer", "Relapsed Cervix Carcinoma", "Cervical cancer recurrent", "Recurrent Cervical Cancer", "Carcinoma cervix recurrent", "Cervix carcinoma recurrent", "cervical cancer, recurrent", "Relapsed Cervical Carcinoma", "Cervical carcinoma recurrent", "Cervical Carcinoma Recurrent", "Recurrent Cervical Carcinoma", "Relapsed Carcinoma of Cervix", "Recurrent Carcinoma of Cervix", "Cervix uteri cancer recurrent", "recurrent cancer of the cervix", "Relapsed Cervix Uteri Carcinoma", "cancer of the cervix, recurrent", "recurrent uterine cervix cancer", "Relapsed Carcinoma of the Cervix", "uterine cervix cancer, recurrent", "Recurrent Cervix Uteri Carcinoma", "recurrent carcinoma of the cervix", "Relapsed Uterine Cervix Carcinoma", "Recurrent Carcinoma of the Cervix", "Relapsed Carcinoma of Cervix Uteri", "carcinoma of the cervix, recurrent", "uterine cervical cancer, recurrent", "Recurrent Uterine Cervix Carcinoma", "Carcinoma uterine cervix recurrent", "Recurrent Carcinoma of Cervix Uteri", "Relapsed Carcinoma of Uterine Cervix", "Recurrent Carcinoma of Uterine Cervix", "Relapsed Carcinoma of the Cervix Uteri", "Recurrent Carcinoma of the Cervix Uteri", "Relapsed Carcinoma of the Uterine Cervix", "Recurrent Carcinoma of the Uterine Cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervix carcinoma recurrent", "shortest_name_length": 23}
{"curie": "UMLS:C0677861", "names": ["Bilateral Cancer", "Bilateral Malignant Tumor", "Bilateral Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bilateral Malignant Neoplasm", "shortest_name_length": 16}
{"curie": "UMLS:C5206665", "names": ["Penile Leiomyoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Penile Leiomyoma", "shortest_name_length": 16}
{"curie": "MONDO:0015427", "names": ["paroxysmal dyskinesia", "Choreoathetosis, episodic", "Paroxysmal choreoathetosis", "paroxysmal choreoathetosis", "Choreoathetosis, paroxysmal", "Choreoathetosis, intermittent", "paroxysmal dystonic choreoathetosis", "Paroxysmal choreoathetosis (disorder)", "paroxysmal choreoathetosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paroxysmal dyskinesia", "shortest_name_length": 21}
{"curie": "UMLS:C0275652", "names": ["Acute gonococcal urethritis", "Urethritis gonococcal acute", "Gonococcal urethritis acute", "urethritis gonococcus, acute", "Neisseria gonorrheae urethritis acute", "Neisseria gonorrhoeae urethritis acute", "Acute gonococcal urethritis (disorder)", "Acute gonococcal urethritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute gonococcal urethritis", "shortest_name_length": 27}
{"curie": "MONDO:0008158", "names": ["Gunal-Seber-Basaran syndrome", "Gunal Seber Basaran syndrome", "dacryocystitis osteopoikilosis", "Dacryocystitis osteopoikilosis", "Osteopoikilosis and dacryocystitis", "OSTEOPOIKILOSIS AND DACRYOCYSTITIS", "osteopoikilosis and dacryocystitis", "dacryocystitis-osteopoikilosis syndrome", "Dacryocystitis-osteopoikilosis syndrome", "Dacryocystitis and osteopoikilosis syndrome", "Dacryocystitis and osteopoikilosis syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dacryocystitis-osteopoikilosis syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0008800", "names": ["OAS", "MLA", "Waardenburg syndrome 3", "Anophthalmia-Syndactyly", "Anophthalmos-syndactyly", "anophthalmia-syndactyly", "Anophthalmia-syndactyly", "ANOPHTHALMIA-SYNDACTYLY", "anophthalmos-syndactyly", "crooked fingers syndrome", "ophthalmoacromelic syndrome", "Ophthalmoacromelic syndrome", "OPHTHALMOACROMELIC SYNDROME", "Ophthalmo-acromelic syndrome", "ophthalmo-acromelic syndrome", "syndactyly-anophthalmos syndrome", "Anophthalmos with limb anomalies", "Syndactyly-anophthalmos syndrome", "anophthalmos with limb anomalies", "anophthalmos-syndactyly syndrome", "Anophthalmia-syndactyly syndrome", "anophthalmia-syndactyly syndrome", "Waardenburg Anophthalmia Syndrome", "MICROPHTHALMIA AND LIMB ANOMALIES", "anophthalmia-Waardenburg syndrome", "Anophthalmia-Waardenburg syndrome", "anophthalmia Waardenburg syndrome", "Anophthalmia Waardenburg syndrome", "Waardenburg anophthalmia syndrome", "WAARDENBURG ANOPHTHALMIA SYNDROME", "MICROPHTHALMIA WITH LIMB ANOMALIES", "Microphthalmia With Limb Anomalies", "microphthalmia with limb anomalies", "Microphthalmia with limb anomalies", "anophthalmos-limb anomalies syndrome", "Anophthalmos-limb anomalies syndrome", "Ophthalmo-acromelic syndrome (disorder)", "Waardenburg recessive anophthalmia syndrome", "anophthalmia-hand-foot defects-mental retardation syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microphthalmia with limb anomalies", "shortest_name_length": 3}
{"curie": "MONDO:0014141", "names": ["MDDGB14", "congenital muscular dystrophy GMPPB-related", "congenital muscular dystrophy-GMPPB related", "muscular dystrophy, congenital, GMPPB-related", "MUSCULAR DYSTROPHY, CONGENITAL, GMPPB-RELATED", "muscular dystrophy-dystroglycanopathy type B14", "muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 14", "muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B14", "muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B, 14", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH IMPAIRED INTELLECTUAL DEVELOPMENT), TYPE B, 14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B14", "shortest_name_length": 7}
{"curie": "MONDO:0001936", "names": ["Brawny scleritis", "brawny scleritis", "Diffuse scleritis", "Brawny scleritis (disorder)", "brawny scleritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brawny scleritis", "shortest_name_length": 16}
{"curie": "UMLS:C5446613", "names": ["Advanced Primary Malignant Brain Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Primary Malignant Brain Neoplasm", "shortest_name_length": 41}
{"curie": "MONDO:0008328", "names": ["GLC1P", "Pseudoglaucoma", "GLAUCOMA 1, OPEN ANGLE, P", "Glaucoma 1, Open Angle, P", "glaucoma 1, open angle, P", "glaucoma 1, open angle, type P"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glaucoma 1, open angle, P", "shortest_name_length": 5}
{"curie": "UMLS:C4523983", "names": ["Foreign body in reproductive tract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Foreign body in reproductive tract", "shortest_name_length": 34}
{"curie": "UMLS:C1827129", "names": ["Allergy, Wasp", "Wasp Venom Allergy", "Wasp Sting Allergy", "Sting Allergy, Wasp", "Allergy, Wasp Sting", "Wasp Sting Allergies", "Allergy to wasp venom", "allergy to wasp venom", "Wasp Sting Hypersensitivity", "Hypersensitivity, Wasp Sting", "Sting Hypersensitivity, Wasp", "Wasp Sting Hypersensitivities", "allergy to wasp venom (history)", "Allergy to wasp venom (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wasp Sting Allergy", "shortest_name_length": 13}
{"curie": "MONDO:0015536", "names": ["Papular xanthoma", "papular xanthoma", "Papular xanthoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papular xanthoma", "shortest_name_length": 16}
{"curie": "MONDO:0005986", "names": ["Torovirus Infection", "Torovirus Infections", "Infection, Torovirus", "Infections, Torovirus", "Torovirus infectious disease", "torovirus infectious disease", "Torovirus disease or disorder", "Torovirus caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "torovirus infectious disease", "shortest_name_length": 19}
{"curie": "UMLS:C0333383", "names": ["Subacute inflammation", "Subacute Inflammation", "Inflammation, subacute", "Subacute Inflammations", "SUBACUTE INFLAMMATIONS", "Subacute inflammation, NOS", "Chronic active inflammation", "Active Chronic Inflammation", "Chronic Active Inflammation", "Active chronic inflammation", "Acute and chronic inflammation", "Acute and Chronic Inflammations", "Active chronic inflammation, NOS", "Acute and chronic inflammation, NOS", "Subacute inflammatory cell infiltrate", "Subacute inflammatory cell infiltration", "Inflammatory cell infiltration, subacute", "Subacute inflammatory cell infiltrate, NOS", "Subacute inflammatory cell infiltration, NOS", "Acute and chronic inflammation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute and chronic inflammation", "shortest_name_length": 21}
{"curie": "MONDO:0019912", "names": ["UPD(6)mat", "maternal uniparental disomy chromosome 6", "maternal uniparental disomy of chromosome 6", "Maternal uniparental disomy of chromosome 6", "maternal uniparental disomy of chromosome type 6", "Maternal uniparental disomy of chromosome 6 (disorder)", "Maternal uniparental disomy of chromosome 6 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maternal uniparental disomy of chromosome 6", "shortest_name_length": 9}
{"curie": "UMLS:C5418891", "names": ["Advanced Ovarian Endometrioid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Ovarian Endometrioid Adenocarcinoma", "shortest_name_length": 44}
{"curie": "MONDO:0032784", "names": ["NEDNEH", "NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND NONEPILEPTIC HYPERKINETIC MOVEMENTS", "neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements", "shortest_name_length": 6}
{"curie": "MONDO:0019091", "names": ["BPD", "ventilator lung; newborn", "Respiratory insufficiency", "bronchopulmonary dysplasia", "Bronchopulmonary dysplasia", "Ventilator lung in newborn", "Bronchopulmonary Dysplasia", "BRONCHOPULMONARY DYSPLASIA", "Dysplasia, Bronchopulmonary", "dysplasia; bronchopulmonary", "bronchopulmonary; dysplasia", "Neonatal chronic lung disease", "chronic lung disease of babies", "bronchopulmonary dysplasia (BPD)", "BPD - Bronchopulmonary dysplasia", "Chronic lung disease of prematurity", "neonatal chronic respiratory disease", "Perinatal bronchopulmonary dysplasia", "Bronchopulmonary dysplasia of newborn", "bronchopulmonary dysplasia of fetus or newborn", "Bronchopulmonary dysplasia of newborn (disorder)", "bronchopulmonary dysplasia of fetus or newborn (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bronchopulmonary dysplasia", "shortest_name_length": 3}
{"curie": "UMLS:C5419582", "names": ["Refractory Grade 2 Follicular Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Grade 2 Follicular Lymphoma", "shortest_name_length": 38}
{"curie": "UMLS:C5555678", "names": ["High Risk Barrett Esophagus", "High-Risk Barrett Esophagus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Risk Barrett Esophagus", "shortest_name_length": 27}
{"curie": "UMLS:C0278554", "names": ["cancer rectal recurrent", "Rectal cancer recurrent", "recurrent rectal cancer", "recurrent rectum cancer", "Recurrent Rectal Cancer", "rectal cancer, recurrent", "rectum cancer, recurrent", "Rectal Cancer, Recurrent", "Rectal carcinoma recurrent", "Recurrent Cancer of Rectum", "Carcinoma rectum recurrent", "Recurrent Rectal Carcinoma", "Carcinoma of rectum recurrent", "Recurrent Cancer of the Rectum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Rectal Cancer", "shortest_name_length": 23}
{"curie": "MONDO:0013970", "names": ["BCKDKD", "Bckdk deficiency", "BCKDK deficiency", "BCKDK DEFICIENCY", "branched-chain KETO acid dehydrogenase KINASE deficiency", "branched-chain keto acid dehydrogenase kinase deficiency", "BRANCHED-CHAIN KETO ACID DEHYDROGENASE KINASE DEFICIENCY", "autism-epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency", "autism - epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "branched-chain keto acid dehydrogenase kinase deficiency", "shortest_name_length": 6}
{"curie": "UMLS:C2931107", "names": ["Myasthenic syndrome, congenital, type IIa", "Myasthenic syndrome, congenital, postsynaptic slow-channel"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myasthenic syndrome, congenital, postsynaptic slow-channel", "shortest_name_length": 41}
{"curie": "MONDO:0021516", "names": ["Benign Glottis Tumor", "benign glottis tumor", "benign glottis neoplasm", "Benign Tumor of Glottis", "benign tumor of glottis", "Benign tumor of glottis", "Benign Glottis Neoplasm", "glottis benign neoplasm", "Benign tumour of glottis", "Benign neoplasm of glottis", "benign neoplasm of glottis", "Benign Neoplasm of Glottis", "Benign Tumor of the Glottis", "benign tumor of the glottis", "Benign Neoplasm of the Glottis", "benign neoplasm of the glottis", "Benign neoplasm of glottis (disorder)", "benign neoplasm of glottis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of glottis", "shortest_name_length": 20}
{"curie": "MONDO:0020538", "names": ["malignant ovarian dysgerminoma", "dysgerminomatous germ cell cancer of ovary", "dysgerminomatous germ cell cancer of the ovary", "malignant dysgerminomatous germ cell tumor of ovary", "malignant dysgerminomatous germ cell tumor of the ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant dysgerminomatous germ cell tumor of ovary", "shortest_name_length": 30}
{"curie": "UMLS:C5206250", "names": ["Unresectable Pancreatic Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Pancreatic Adenocarcinoma", "shortest_name_length": 38}
{"curie": "UMLS:C1332303", "names": ["Anterior Tongue Adenoid Cystic Carcinoma", "Adenoid Cystic Carcinoma of Anterior Tongue", "Adenoid Cystic Carcinoma of the Anterior Tongue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anterior Tongue Adenoid Cystic Carcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0000515", "names": ["bone chondrosarcoma", "bone tissue chondrosarcoma (disease)", "chondrosarcoma (disease) of bone tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bone chondrosarcoma", "shortest_name_length": 19}
{"curie": "UMLS:C0339823", "names": ["Nasal cyst", "nasal cyst", "cysts nasal", "cyst; antrum", "antrum; cyst", "Intranasal cyst", "Nasal Cavity Cyst", "Cyst of Nasal Cavity", "Cyst of nasal cavity", "nasal cyst (diagnosis)", "Cyst of the Nasal Cavity", "Cyst of nasal cavity (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cyst of nasal cavity", "shortest_name_length": 10}
{"curie": "MONDO:0005933", "names": ["PPB", "PPBFTDS", "Lung Blastoma", "lung blastoma", "pneumoblastoma", "Pneumoblastoma", "Blastoma of lung", "blastoma of lung", "Blastoma of Lung", "PULMONARY BLASTOMA", "pulmonary blastoma", "Pulmonary Blastoma", "Pulmonary blastoma", "Pulmonary Blastomas", "Blastoma, Pulmonary", "blastoma of the lung", "Blastomas, Pulmonary", "Blastoma of the Lung", "[M] Pulmonary blastoma", "Pleuropulmonary blastoma", "pleuropulmonary blastoma", "PLEUROPULMONARY BLASTOMA", "Pleuropulmonary Blastoma", "Pleuro-pulmonary blastoma", "Pulmonary blastoma (disorder)", "Carcinosarcoma, embryonal type", "Pulmonary Blastoma of Childhood", "Pleuropulmonary blastoma (disorder)", "PPB FAMILIAL TUMOR AND DYSPLASIA SYNDROME", "Pulmonary blastoma (morphologic abnormality)", "Pleuropulmonary blastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary blastoma", "shortest_name_length": 3}
{"curie": "MONDO:0009369", "names": ["NIHF", "non-immune HF", "Non-immune HF", "Nonimmune hydrops", "Non-immune fetal edema", "non-immune fetal edema", "Non-immune fetal hydrops", "Nonimmune Hydrops Fetali", "non-immune fetal hydrops", "Nonimmune hydrops fetalis", "Non-immune foetal hydrops", "Nonimmune Hydrops Fetalis", "Hydrops Fetalis Nonimmune", "Hydrops Fetali, Nonimmune", "Idiopathic Hydrops Fetali", "Hydrops Fetalis, Nonimmune", "Fetali, Idiopathic Hydrops", "Non-Immune Hydrops Fetalis", "HYDROPS FETALIS NON IMMUNE", "non immune hydrops fetalis", "Fetalis Nonimmune, Hydrops", "Idiopathic hydrops fetalis", "Hydrops fetalis, nonimmune", "Nonimmune, Hydrops Fetalis", "Idiopathic Hydrops Fetalis", "HYDROPS FETALIS, NONIMMUNE", "Hydrops Fetali, Idiopathic", "hydrops fetalis, nonimmune", "Non-immune hydrops fetalis", "Hydrops Fetalis Nonimmunes", "non-immune hydrops fetalis", "Idiopathic hydrops foetalis", "Nonimmunes, Hydrops Fetalis", "Hydrops Fetalis, Idiopathic", "Hydrops Fetalis, Non-Immune", "Fetalis, Idiopathic Hydrops", "Non-immune hydrops foetalis", "Fetalis Nonimmunes, Hydrops", "Hydrops fetalis, non-immune", "nonisoimmunized hydrops fetalis", "Familial Non Immune Hydrops Fetalis", "Familial Non-Immune Hydrops Fetalis", "Idiopathic hydrops fetalis (disorder)", "Non-immune hydrops fetalis (disorder)", "Hemoglobin H hydrops fetalis syndrome", "HEMOGLOBIN H HYDROPS FETALIS SYNDROME", "Hydrops fetalis not due to isoimmunization", "hydrops fetalis, Alpha-thalassemia-related", "HYDROPS FETALIS, ALPHA-THALASSEMIA-RELATED", "Hydrops fetalis not due to isoimmunisation", "Hydrops foetalis not due to isoimmunisation", "nonisoimmunized hydrops fetalis (diagnosis)", "Hydrops foetalis not due to isoimmunization"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-immune hydrops fetalis", "shortest_name_length": 4}
{"curie": "MONDO:0010998", "names": ["CDG1D", "CDGId", "CDG 1D", "CDG Id", "CDG-Id", "ALG3-CDG", "CDGS, type IV", "CDGS4, FORMERLY", "CDGS4 (formerly)", "ALG3-CDG (CDG-Id)", "CDG syndrome type Id", "CDGS, TYPE IV, FORMERLY", "CDGS, type IV, formerly", "Mannosyltransferase 6 deficiency", "mannosyltransferase 6 deficiency", "congenital disorder of glycosylation Id", "congenital disorder of glycosylation 1d", "ALG3-congenital disorder of glycosylation", "ALG3 congenital disorder of glycosylation", "Congenital disorder of glycosylation type 1D", "congenital disorder of glycosylation type Id", "Congenital Disorder of Glycosylation Type Id", "Congenital disorder of glycosylation type 1d", "congenital disorder of glycosylation type 1d", "Congenital disorder of glycosylation type Id", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id", "congenital disorder of glycosylation, type Id", "Congenital Disorder Of Glycosylation, Type ID", "carbohydrate deficient glycoprotein syndrome type Id", "Carbohydrate-deficient glycoprotein syndrome, type 4", "Carbohydrate deficient glycoprotein syndrome type Id", "carbohydrate-deficient glycoprotein syndrome, type IV", "carbohydrate-deficient glycoprotein syndrome type IV (formerly)", "carbohydrate-deficient glycoprotein syndrome, type IV, formerly", "CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME, TYPE IV, FORMERLY", "Asparagine-linked glycosylation 3 congenital disorder of glycosylation", "Asparagine-linked glycosylation 3 congenital disorder of glycosylation (disorder)", "ALG3-CDG - asparagine-linked glycosylation 3 congenital disorder of glycosylation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ALG3-congenital disorder of glycosylation", "shortest_name_length": 5}
{"curie": "MONDO:0007967", "names": ["Melanoma-Astrocytoma Syndrome", "MELANOMA-ASTROCYTOMA SYNDROME", "melanoma astrocytoma syndrome", "Melanoma-astrocytoma syndrome", "melanoma-astrocytoma syndrome", "Melanoma astrocytoma syndrome", "Melanoma and Neural System Tumor Syndrome", "melanoma and neural system tumor syndrome", "Melanoma and neural system tumor syndrome", "MELANOMA AND NEURAL SYSTEM TUMOR SYNDROME", "Melanoma and neural system tumour syndrome", "Melanoma and neural system tumor syndrome (disorder)", "Cutaneous malignant melanoma and cerebral astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melanoma and neural system tumor syndrome", "shortest_name_length": 29}
{"curie": "UMLS:C0270088", "names": ["Tentorial tear", "Tentorial Tear", "injury; birth, tentorial tear", "birth; injury, tentorial tear", "Tentorial tear as birth trauma", "Tentorial tear due to birth injury", "Tentorial tear due to birth trauma", "tentorial tear due to birth trauma", "Tentorial laceration due to birth trauma", "Tentorial tear due to birth trauma (disorder)", "tentorial tear due to birth trauma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tentorial tear due to birth trauma", "shortest_name_length": 14}
{"curie": "UMLS:C0349467", "names": ["Transient myocardial ischemia in newborn", "Transient Myocardial Ischemia of Newborn", "Transient myocardial ischemia of newborn", "Transient myocardial ischaemia of newborn", "ischemia; myocardial, transient, of newborn", "Transient myocardial ischemia of newborn (disorder)", "Transient myocardial ischemia of newborn (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transient myocardial ischemia of newborn", "shortest_name_length": 40}
{"curie": "UMLS:C0279580", "names": ["L1 pediatric ALL", "L1 childhood ALL", "ALL, L1 pediatric", "ALL, pediatric L1", "ALL, L1 childhood", "ALL, childhood L1", "pediatric ALL, L1", "childhood ALL, L1", "L1 Acute Lymphoblastic Leukemia", "L1 childhood acute lymphocytic leukemia", "L1 pediatric acute lymphocytic leukemia", "childhood acute lymphocytic leukemia, L1", "L1 lymphocytic leukemia, acute childhood", "L1 acute lymphocytic leukemia, childhood", "pediatric acute lymphocytic leukemia, L1", "acute lymphocytic leukemia, childhood L1", "Childhood L1 Acute Lymphoblastic Leukemia", "L1 childhood acute lymphoblastic leukemia", "leukemia, childhood acute lymphocytic , L1", "childhood acute lymphoblastic leukemia, L1", "acute lymphoblastic leukemia, childhood L1", "pediatric acute lymphoblastic leukemia, L1", "L1 acute lymphoblastic leukemia, childhood", "L1 lymphoblastic leukemia, acute childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood L1 Acute Lymphoblastic Leukemia", "shortest_name_length": 16}
{"curie": "UMLS:C0677952", "names": ["Stage II Hodgkin Lymphoma", "Hodgkin's Disease Stage II", "Stage II Hodgkin's Disease", "Hodgkin's disease stage II", "Stage II Hodgkin's Lymphoma", "Hodgkin's Lymphoma Stage II", "Hodgkin's disease NOS stage II", "Ann Arbor Stage II Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Hodgkin Lymphoma", "shortest_name_length": 25}
{"curie": "UMLS:C4329279", "names": ["Adipsic Diabetes Insipidus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adipsic Diabetes Insipidus", "shortest_name_length": 26}
{"curie": "UMLS:C0079747", "names": ["Low Grade Lymphoma", "Low-Grade Lymphoma", "lymphoma low grade", "low-grade lymphoma", "low grade lymphoma", "Low grade lymphoma", "grade low lymphomas", "Low-Grade Lymphomas", "Lymphoma, Low-Grade", "Lymphoma, Low Grade", "Low Grade Lymphoma (neoplasm)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Grade Lymphoma (neoplasm)", "shortest_name_length": 18}
{"curie": "UMLS:C0334036", "names": ["Apocrine Metaplasia", "apocrine metaplasia", "Apocrine metaplasia", "apocrine; metaplasia", "metaplasia; apocrine", "Metaplasia, apocrine", "Apocrine metaplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Apocrine metaplasia", "shortest_name_length": 19}
{"curie": "MONDO:0011386", "names": ["MVCD1", "NEUROPATHY, DIABETIC, SUSCEPTIBILITY TO", "neuropathy, diabetic, susceptibility to", "nephropathy, diabetic, susceptibility to", "NEPHROPATHY, DIABETIC, SUSCEPTIBILITY TO", "microvascular complications of diabetes 1", "END-STAGE RENAL DISEASE, DIABETIC, SUSCEPTIBILITY TO", "end-stage renal disease, diabetic, susceptibility to", "proliferative retinopathy, diabetic, susceptibility to", "PROLIFERATIVE RETINOPATHY, DIABETIC, SUSCEPTIBILITY TO", "NONPROLIFERATIVE RETINOPATHY, DIABETIC, SUSCEPTIBILITY TO", "nonproliferative retinopathy, diabetic, susceptibility to", "MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO", "microvascular complications of diabetes, susceptibility to", "MICROVASCULAR COMPLICATIONS OF DIABETES, PROTECTION AGAINST", "microvascular complications of diabetes, protection against", "MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 1", "microvascular complications of diabetes, susceptibility to, 1", "VEGFA microvascular complications of diabetes, susceptibility", "END-STAGE RENAL DISEASE, DIABETIC, SUSCEPTIBILITY TO (finding)", "PROLIFERATIVE RETINOPATHY, DIABETIC, SUSCEPTIBILITY TO (finding)", "microvascular complications of diabetes, susceptibility to, type 1", "NONPROLIFERATIVE RETINOPATHY, DIABETIC, SUSCEPTIBILITY TO (finding)", "MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 1(finding)", "microvascular complications of diabetes, susceptibility caused by mutation in VEGFA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microvascular complications of diabetes, susceptibility to, 1", "shortest_name_length": 5}
{"curie": "MONDO:0010279", "names": ["TOD", "ODPF", "Odpd", "ODPD", "TODPD", "ODPF SYNDROME", "ODPF syndrome", "Odpf syndrome", "terminal osseous dysplasia", "TERMINAL OSSEOUS DYSPLASIA", "terminal osseous dysplasia, X-linked dominant", "terminal osseous dysplasia and pigmentary defects", "Terminal Osseous Dysplasia and Pigmentary Defects", "TERMINAL OSSEOUS DYSPLASIA AND PIGMENTARY DEFECTS", "terminal osseous dysplasia-pigmentary defects syndrome", "digital osseous dysplasia with facial pigmentary defects and multiple frenula", "OSSEOUS DYSPLASIA, DIGITAL, WITH FACIAL PIGMENTARY DEFECTS AND MULTIPLE FRENULA", "osseous dysplasia, digital, with Facial pigmentary defects and multiple frenula", "Osseous Dysplasia, Digital, with Facial Pigmentary Defects and Multiple Frenula"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "terminal osseous dysplasia-pigmentary defects syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0012469", "names": ["MYP14", "Myopia 14", "myopia 14", "MYOPIA 14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopia 14", "shortest_name_length": 5}
{"curie": "MONDO:0008288", "names": ["BAKER CYST", "Baker Cyst", "baker cyst", "Baker Cysts", "bakers cyst", "Baker; cyst", "cyst; Baker", "Cyst;Bakers", "Cyst, Baker", "Baker's cyst", "Cysts, Baker", "baker's cyst", "BAKER'S CYST", "Baker's Cyst", "baker's cysts", "Popliteal Cyst", "Cyst;popliteal", "popliteal cyst", "POPLITEAL CYST", "Popliteal cyst", "cyst; popliteal", "Cyst, Popliteal", "popliteal cysts", "popliteal; cyst", "Popliteal Cysts", "Cysts, Popliteal", "Baker's cyst of knee", "cyst; synovial, Baker", "synovial cyst of knee", "Synovial cyst of knee", "synovial; cyst, Baker", "Popliteal synovial cyst", "knee cyst popliteal (___cm)", "synovial cyst of popliteal space", "Synovial cyst of popliteal space", "Synovial cyst of knee (disorder)", "popliteal cyst (physical finding)", "Synovial cyst of popliteal space [Baker]", "synovial cyst of popliteal space (diagnosis)", "Synovial cyst of popliteal space [Baker], unspecified knee"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "popliteal cyst", "shortest_name_length": 10}
{"curie": "UMLS:C4553875", "names": ["Stage IVB Differentiated Thyroid Gland Cancer", "Stage IVB Differentiated Thyroid Gland Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Differentiated Thyroid Gland Carcinoma AJCC v8", "shortest_name_length": 45}
{"curie": "MONDO:0002981", "names": ["PNET of bone stage unspecified", "bone peripheral neuroepithelioma", "Bone Peripheral Neuroepithelioma", "peripheral neuroepithelioma of bone", "osseous peripheral Neuroepithelioma", "Osseous Peripheral Neuroepithelioma", "osseous peripheral neuroepithelioma", "Peripheral neuroepithelioma of bone", "Peripheral Neuroepithelioma of Bone", "Peripheral neuroepithelioma of bone NOS", "Peripheral Neuroepithelioma of the Bone", "peripheral neuroepithelioma of the bone", "Peripheral Neuroectodermal Tumor of Bone", "peripheral neuroectodermal tumor of bone", "peripheral neuroectodermal tumor of the bone", "Peripheral Neuroectodermal Tumor of the Bone", "Peripheral primitive neuroectodermal bone tumor", "Peripheral primitive neuroectodermal bone tumour", "Peripheral Primitive Neuroectodermal Tumor of Bone", "peripheral primitive neuroectodermal tumor of bone", "peripheral neuroectodermal tumor of bone (diagnosis)", "bone tissue peripheral primitive neuroectodermal tumor", "peripheral primitive neuroectodermal tumor of bone tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peripheral primitive neuroectodermal tumor of bone", "shortest_name_length": 30}
{"curie": "UMLS:C5206694", "names": ["Locally Advanced Ureter Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Ureter Urothelial Carcinoma", "shortest_name_length": 44}
{"curie": "MONDO:0012118", "names": ["CDG2E", "CDGIIE", "CDGIIe", "CDG 2E", "CDG IIe", "CDG IIE", "CDG-IIe", "COG7-CDG", "COG7-CDG (CDG-IIe)", "CDG syndrome type IIe", "COG7 congenital disorder of glycosylation", "COG7-congenital disorder of glycosylation", "congenital disorder of glycosylation type 2e", "Congenital disorder of glycosylation type 2e", "Congenital disorder of glycosylation type 2E", "congenital disorder of glycosylation type IIe", "Congenital disorder of glycosylation type IIe", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe", "congenital disorder of glycosylation, type IIe", "Congenital Disorder Of Glycosylation, Type IIE", "carbohydrate deficient glycoprotein syndrome type IIe", "Carbohydrate deficient glycoprotein syndrome type IIe", "Component of oligomeric golgi complex 7 congenital disorder of glycosylation", "COG7 (component of oligomeric golgi complex 7) congenital disorder of glycosylation", "Component of oligomeric golgi complex 7 congenital disorder of glycosylation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "COG7-congenital disorder of glycosylation", "shortest_name_length": 5}
{"curie": "MONDO:0017469", "names": ["congenital elbow dislocation", "congenital radial head dislocation", "isolated congenital elbow dislocation", "isolated congenital radial head dislocation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital elbow dislocation", "shortest_name_length": 28}
{"curie": "MONDO:0600003", "names": ["bacterial hemorrhagic fever", "bacterial haemorrhagic fever", "haemorrhagic fever, bacterial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bacterial hemorrhagic fever", "shortest_name_length": 27}
{"curie": "UMLS:C1707409", "names": ["Clear Cell Variant Thyroid Gland Follicular Carcinoma", "Thyroid Gland Follicular Carcinoma, Clear Cell Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Follicular Carcinoma, Clear Cell Variant", "shortest_name_length": 53}
{"curie": "UMLS:C4744375", "names": ["Sellar Chondroid Chordoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sellar Chondroid Chordoma", "shortest_name_length": 25}
{"curie": "MONDO:0044874", "names": ["RCC", "Refractory Cytopenia of Childhood", "Refractory cytopenia of childhood", "refractory cytopenia of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "refractory cytopenia of childhood", "shortest_name_length": 3}
{"curie": "MONDO:0011747", "names": ["DYX5", "dyslexia, susceptibility to, 5", "DYSLEXIA, SUSCEPTIBILITY TO, 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyslexia, susceptibility to, 5", "shortest_name_length": 4}
{"curie": "MONDO:0003401", "names": ["Yolk Sac tumor of the CNS", "yolk Sac tumor of the CNS", "Yolk Sac tumour of the CNS", "childhood CNS yolk sac tumor", "childhood CNS endodermal sinus tumor", "central nervous system yolk Sac tumor", "central nervous system yolk sac tumor", "Central Nervous System Yolk Sac Tumor", "central nervous system endodermal sinus tumor", "central nervous system endodermal sinus tumour", "childhood central nervous system yolk Sac tumor", "pediatric central nervous system yolk Sac tumor", "Childhood Central Nervous System Yolk Sac Tumor", "pediatric central nervous system Yolk Sac tumor", "Pediatric Central Nervous System Yolk Sac Tumor", "childhood central nervous system yolk sac tumor", "paediatric central nervous system Yolk Sac tumour", "Childhood Central Nervous System Yolk Sac Neoplasm", "Pediatric Central Nervous System Yolk Sac Neoplasm", "childhood central nervous system yolk Sac neoplasm", "pediatric central nervous system yolk Sac neoplasm", "Pediatric Central Nervous System Endodermal Sinus Tumor", "Childhood Central Nervous System Endodermal Sinus Tumor", "childhood central nervous system endodermal sinus tumor", "Pediatric Central Nervous System Endodermal Sinus Neoplasm", "Childhood Central Nervous System Endodermal Sinus Neoplasm", "pediatric central nervous system endodermal sinus neoplasm", "childhood central nervous system endodermal sinus neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system endodermal sinus tumor", "shortest_name_length": 25}
{"curie": "MONDO:0017656", "names": ["motor stereotypies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "motor stereotypies", "shortest_name_length": 18}
{"curie": "MONDO:0017532", "names": ["postaxial polydactyly type A, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postaxial polydactyly type A, bilateral", "shortest_name_length": 39}
{"curie": "UMLS:C5204294", "names": ["Warty-Basaloid Carcinoma of the Penis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Warty-Basaloid Carcinoma of the Penis", "shortest_name_length": 37}
{"curie": "UMLS:C5447370", "names": ["Refractory Breast Implant-Associated Anaplastic Large Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Breast Implant-Associated Anaplastic Large Cell Lymphoma", "shortest_name_length": 67}
{"curie": "MONDO:0017721", "names": ["Sandhoff disease, infantile form", "infantile GM2 gangliosidosis 0 variant", "Hexosaminidases A and B deficiency, infantile form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sandhoff disease, infantile form", "shortest_name_length": 32}
{"curie": "MONDO:0015490", "names": ["predominantly small-vessel vasculitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "predominantly small-vessel vasculitis", "shortest_name_length": 37}
{"curie": "MONDO:0005161", "names": ["HPV", "HPV Infection", "HPV infection", "HPV Infections", "papillomavirus infection", "Papillomavirus infection", "Papillomavirus Infection", "Papilloma virus infection", "Papilloma viral infection", "Papillomavirus Infections", "Papilloma viral infections", "Papilloma viral infection NOS", "Disease due to Papillomavirus", "Human Papillomavirus Infection", "Human Papillomavirus infection", "Disease due to Papilloma virus", "Human papillomavirus infection", "HUMAN PAPILLOMA VIRUS INFECTION", "Human Papillomavirus Infections", "Human Papilloma Virus Infection", "Human papilloma Virus infection", "human papilloma virus infection", "Human papilloma virus infection", "Papillomavirus Infection, Human", "Papillomavirus Infections, Human", "human infections papilloma virus", "Disease caused by Papillomavirus", "Disease caused by Papilloma virus", "HPV (Human papillomavirus) disease", "Disease due to Papilloma virus, NOS", "Human papilloma virus infection, NOS", "HPV (Human papillomavirus) infection", "Human papillomavirus infectious disease", "Human papillomavirus disease or disorder", "Human papillomavirus infection (disorder)", "human papilloma virus infection (diagnosis)", "Disease caused by Papillomavirus (disorder)", "Human papillomavirus caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "human papilloma virus infection", "shortest_name_length": 3}
{"curie": "EFO:1001514", "names": ["endometrial endometrioid carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometrial endometrioid carcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0700121", "names": ["ACTL6A-related BAFopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ACTL6A-related BAFopathy", "shortest_name_length": 24}
{"curie": "UMLS:C0752048", "names": ["Hypocatalasia", "Hypocatalasemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypocatalasemia", "shortest_name_length": 13}
{"curie": "UMLS:C0685897", "names": ["Acephalostomia", "ACEPHALOSTOMIA", "Acephalostomia (disorder)", "Acephalostomia (diagnosis)", "congenital musculoskeletal deformity head acephalostomia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acephalostomia", "shortest_name_length": 14}
{"curie": "UMLS:C1519721", "names": ["Typical Ovarian Thecoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Typical Ovarian Thecoma", "shortest_name_length": 23}
{"curie": "UMLS:C0424566", "names": ["Hyposomnia", "hyposomnia", "Short of sleep", "short sleeping", "Hyposomnia, NOS", "getting enough sleep", "Hyposomnia (diagnosis)", "Not getting enough sleep", "sleep disorder hyposomnia", "Insufficient Sleep Syndrome", "insufficient sleep syndrome", "Insufficient sleep syndrome", "Insufficient Sleep Syndromes", "Syndrome, Insufficient Sleep", "Not getting enough sleep (disorder)", "insufficient sleep syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Not getting enough sleep", "shortest_name_length": 10}
{"curie": "UMLS:C1336508", "names": ["Storiform-Pleomorphic Malignant Fibrous Histiocytoma NCI Grade 2", "Storiform-Pleomorphic Malignant Fibrous Histiocytoma NCI Grade II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Storiform-Pleomorphic Malignant Fibrous Histiocytoma NCI Grade 2", "shortest_name_length": 64}
{"curie": "MONDO:0003688", "names": ["WDPM", "WDPMT", "Benign/Intermediate Mesothelioma", "benign/Intermediate mesothelioma", "benign intermediate mesothelioma", "well differentiated papillary mesothelioma", "Well-differentiated papillary mesothelioma", "Well Differentiated Papillary Mesothelioma", "Well Differentiated Papillary Mesothelial Tumor", "well-differentiated mesothelial papillary tumor", "Well-Differentiated Mesothelial Papillary Tumor", "Well-Differentiated Papillary Mesothelial Tumor", "well-differentiated mesothelial papillary neoplasm", "Well-Differentiated Mesothelial Papillary Neoplasm", "well-differentiated papillary tumor of mesothelium", "Well-Differentiated Papillary Tumor of Mesothelium", "Well-differentiated Papillary tumor of Mesothelium", "Well-Differentiated Papillary Neoplasm of Mesothelium", "well-differentiated papillary neoplasm of mesothelium", "Well-Differentiated Papillary Tumor of the Mesothelium", "well-differentiated papillary tumor of the mesothelium", "well-differentiated papillary neoplasm of the mesothelium", "Well-Differentiated Papillary Neoplasm of the Mesothelium", "Well-differentiated papillary mesothelioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "well differentiated papillary mesothelioma", "shortest_name_length": 4}
{"curie": "UMLS:C5555641", "names": ["Ovarian Smooth Muscle Tumor", "Ovarian Smooth Muscle Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Smooth Muscle Neoplasm", "shortest_name_length": 27}
{"curie": "MONDO:0011843", "names": ["CMH25", "CMD1N, FORMERLY", "CARDIOMYOPATHY, DILATED, 1N", "Cardiomyopathy, Dilated, 1N", "hypertrophic cardiomyopathy 25", "TCAP hypertrophic cardiomyopathy", "cardiomyopathy, hypertrophic, 25", "Tcap hypertrophic cardiomyopathy", "hypertrophic cardiomyopathy type 25", "CARDIOMYOPATHY, DILATED, 1N, FORMERLY", "cardiomyopathy familial hypertrophic 25", "cardiomyopathy, familial hypertrophic, 25", "CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 25", "cardiomyopathy, familial hypertrophic, type 25", "hypertrophic cardiomyopathy caused by mutation in TCAP"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophic cardiomyopathy 25", "shortest_name_length": 5}
{"curie": "UMLS:C0877567", "names": ["Mycobacterium fortuitum infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mycobacterium fortuitum infection", "shortest_name_length": 33}
{"curie": "MONDO:0030026", "names": ["RDLKD", "ACBD5 deficiency", "RETINAL DYSTROPHY WITH LEUKODYSTROPHY", "retinal dystrophy with leukodystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal dystrophy with leukodystrophy", "shortest_name_length": 5}
{"curie": "MONDO:0021383", "names": ["MOUTH FLOOR TUMOR", "mouth floor tumor", "Floor of Mouth Tumor", "floor of mouth tumor", "mouth floor neoplasm", "tumor of mouth floor", "tumor of floor of mouth", "Tumor of Floor of Mouth", "Tumor of floor of mouth", "neoplasm of mouth floor", "Floor of Mouth Neoplasm", "floor of mouth neoplasm", "floor of the mouth tumor", "Tumour of floor of mouth", "Floor of the Mouth Tumor", "Neoplasm of Floor of Mouth", "neoplasm of floor of mouth", "Neoplasm of floor of mouth", "Floor of the Mouth Neoplasm", "floor of the mouth neoplasm", "mouth floor neoplasm (disease)", "tumor of the floor of the mouth", "Tumor of the Floor of the Mouth", "Neoplasm of the Floor of the Mouth", "neoplasm of the floor of the mouth", "Neoplasm of floor of mouth (disorder)", "neoplasm of floor of mouth (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplasm of floor of mouth", "shortest_name_length": 17}
{"curie": "MONDO:0013941", "names": ["spondyloenchondromatosis with D-2-hydroxyglutaric aciduria", "SPONDYLOENCHONDROMATOSIS WITH D-2-HYDROXYGLUTARIC ACIDURIA", "Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria", "metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria", "METAPHYSEAL CHONDROMATOSIS WITH D-2-HYDROXYGLUTARIC ACIDURIA", "METAPHYSEAL ENCHONDRODYSPLASIA WITH 2-HYDROXYGLUTARIC ACIDURIA", "METAPHYSEAL ENCHONDROMATOSIS WITH D-2-HYDROXYGLUTARIC ACIDURIA", "metaphyseal enchondromatosis with D-2-hydroxyglutaric aciduria", "metaphyseal Enchondrodysplasia with 2-hydroxyglutaric aciduria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria", "shortest_name_length": 58}
{"curie": "MONDO:0011121", "names": ["PGL2", "Paragangliomas 2", "PARAGANGLIOMAS 2", "paragangliomas 2", "SDHAF2 paraganglioma", "paragangliomas type 2", "glomus tumors, familial, 2", "Glomus Tumors, Familial, 2", "GLOMUS TUMORS, FAMILIAL, 2", "PARAGANGLIOMAS 2 (disorder)", "paraganglioma caused by mutation in SDHAF2", "SDHAF2-related hereditary paraganglioma-pheochromocytoma syndrome (paragangliomas 2)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paragangliomas 2", "shortest_name_length": 4}
{"curie": "MONDO:0021343", "names": ["Mouth Floor Cancer", "mouth floor cancer", "mouth floor carcinoma", "Floor of Mouth Carcinoma", "floor of mouth carcinoma", "carcinoma of mouth floor", "Carcinoma of Floor of Mouth", "Carcinoma of floor of mouth", "carcinoma of floor of mouth", "Floor of the Mouth Carcinoma", "floor of the mouth carcinoma", "Carcinoma of the Floor of the Mouth", "carcinoma of the floor of the mouth", "carcinoma of floor of mouth (diagnosis)", "Malignant epithelial neoplasm of floor of mouth", "Malignant epithelial neoplasm of floor of mouth (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma of floor of mouth", "shortest_name_length": 18}
{"curie": "MONDO:0002945", "names": ["Micronodular basal cell carcinoma", "micronodular basal cell carcinoma", "Micronodular Basal Cell Carcinoma", "Basal cell carcinoma, micronodular", "Basal cell carcinoma - micronodular", "skin micronodular basal cell carcinoma", "Skin Micronodular Basal Cell Carcinoma", "Basal cell carcinoma - micronodular (disorder)", "Basal cell carcinoma - micronodular (diagnosis)", "malignant neoplasm carcinoma basal cell micronodular", "Basal cell carcinoma, micronodular (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "micronodular basal cell carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0060507", "names": ["RDMS", "retinal dystrophy with macular staphyloma", "retinal dystrophy with or without macular staphyloma", "RETINAL DYSTROPHY WITH OR WITHOUT MACULAR STAPHYLOMA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal dystrophy with or without macular staphyloma", "shortest_name_length": 4}
{"curie": "MONDO:0009975", "names": ["reticulosarcoma", "Reticulosarcoma", "Reticulosarcomas", "lymphoma large cell", "Large cell lymphoma", "LYMPHOMA LARGE CELL", "Reticulosarcoma NOS", "large cell lymphoma", "cell large lymphomas", "histiocytic lymphoma", "Reticulosarcoma, NOS", "large-cell Lymphomas", "histiocytic; lymphoma", "lymphoma; histiocytic", "reticular cell sarcoma", "Reticulum cell sarcoma", "[M]Reticulosarcoma NOS", "Reticulum Cell Sarcoma", "Reticulum-Cell Sarcoma", "RETICULUM CELL SARCOMA", "reticulum cell sarcoma", "Sarcoma, Reticulum Cell", "reticulum cell; sarcoma", "Reticulum-Cell Sarcomas", "cell reticulum sarcomas", "sarcoma; reticulum cell", "cells reticulum sarcoma", "Sarcoma, Reticulum-Cell", "Reticulum Cell Sarcomas", "reticulosarcoma; diffuse", "Reticulosarcoma, diffuse", "diffuse; reticulosarcoma", "sarcoma of reticular cell", "Reticulosarcoma (disorder)", "Reticulosarcoma morphology", "Reticulum cell sarcoma NOS", "Reticulum cell sarcoma, NOS", "reticulosarcoma (diagnosis)", "interdigitating cell sarcoma", "Reticulum cell sarcoma morphol", "large cell lymphoma (diagnosis)", "Malignant lymphoma, histiocytic", "Reticulum cell sarcoma, diffuse", "Reticulum cell sarcoma morphology", "Malignant lymphoma, large cell, NOS", "Malignant lymphoma, histiocytic, NOS", "Malignant lymphoma reticulum cell type", "Malignant lymphoma, reticulum cell type", "Reticulosarcoma morphology (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "reticulum cell sarcoma", "shortest_name_length": 15}
{"curie": "MONDO:0008699", "names": ["achalasia microcephaly", "Achalasia microcephaly", "Achalasia-microcephaly syndrome", "Achalasia microcephaly syndrome", "Achalasia-Microcephaly Syndrome", "achalasia microcephaly syndrome", "ACHALASIA-MICROCEPHALY SYNDROME", "achalasia-microcephaly syndrome", "Achalasia microcephaly syndrome (disorder)", "Achalasia microcephaly syndrome (diagnosis)", "autosomal recessive achalasia microcephaly syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "achalasia microcephaly syndrome", "shortest_name_length": 22}
{"curie": "MONDO:0014128", "names": ["CRS3", "craniosynostosis 3", "CRANIOSYNOSTOSIS 3", "TCF12 craniosynostosis", "craniosynostosis type 3", "TCF12-related craniosynostosis", "craniosynostosis caused by mutation in TCF12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "TCF12-related craniosynostosis", "shortest_name_length": 4}
{"curie": "MONDO:0017832", "names": ["M. xenopi", "Mycobacterium xenopi", "xenopi; Mycobacterium", "Mycobacterium; xenopi", "mycobacterium xenopi infection", "Infection due to Mycobacterium xenopi", "Mycobacterium xenopi infectious disease", "Mycobacterium xenopi disease or disorder", "Infection caused by Mycobacterium xenopi", "Mycobacterium xenopi caused disease or disorder", "Infection caused by Mycobacterium xenopi (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mycobacterium xenopi infection", "shortest_name_length": 9}
{"curie": "MONDO:0020431", "names": ["juxtaposition of the atrial auricles", "juxtaposition of the atrial appendages"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juxtaposition of the atrial appendages", "shortest_name_length": 36}
{"curie": "MONDO:0001103", "names": ["Giardia", "giardia", "Giardiosis", "giardiasis", "Giardiases", "Lambliasis", "Giardiasis", "lambliasis", "GIARDIASIS", "Lambliases", "LAMBLIASIS", "giardiosis", "beaver feaver", "Giardial colitis", "colitis; giardial", "giardial; colitis", "Giardia Infection", "Giardia infection", "giardia infection", "Giardial enteritis", "Giardia infections", "Giardia Infections", "giardia infections", "Infection, Giardia", "infections, Giardia", "Infections, Giardia", "Giardiasis (disorder)", "INTESTINAL GIARDIASIS", "GIARDIASIS INTESTINAL", "giardiasis (diagnosis)", "Giardiasis [lambliasis]", "Infection due to Giardia", "Giardia lamblia infection", "Giardia lamblia; infection", "infection; Giardia lamblia", "infection by Giardia lamblia", "Infection by Giardia lamblia", "infectious; enteritis, giardial", "enteritis; infectious, giardial", "Infection caused by Giardia lamblia", "Infection caused by Giardia lamblia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "giardiasis", "shortest_name_length": 7}
{"curie": "MONDO:0011175", "names": ["FRDA2", "FRIEDREICH ATAXIA 2", "Friedreich ataxia 2", "Friedreich Ataxia 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Friedreich ataxia 2", "shortest_name_length": 5}
{"curie": "MONDO:0014319", "names": ["RHDA2", "renal hypodysplasia/aplasia 2", "RENAL HYPODYSPLASIA/APLASIA 2", "FGF20 renal agenesis (disease)", "renal hypodysplasia/aplasia type 2", "renal agenesis (disease) caused by mutation in FGF20"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal hypodysplasia/aplasia 2", "shortest_name_length": 5}
{"curie": "MONDO:0000327", "names": ["Searl ulcer", "SEARL ULCER", "BURULI ULCER", "Buruli Ulcer", "Buruli ulcer", "buruli ulcer", "ulcer; Buruli", "Mossman ulcer", "Ulcer, Buruli", "Buruli; ulcer", "Daintree ulcer", "Searle's ulcer", "Searles's ulcer", "Bairnsdale ulcer", "Buruli ulcer disease", "Buruli Ulcer Disease", "Ulcer Disease, Buruli", "Buruli Ulcer Diseases", "Disease, Buruli Ulcer", "Diseases, Buruli Ulcer", "Ulcer Diseases, Buruli", "Buruli ulcer (disorder)", "Buruli ulcer (diagnosis)", "MYCOBACTERIUM ULCERANS INFECTION", "Mycobacterium ulcerans infection", "Mycobacterium ulcerans Infection", "Infection, Mycobacterium ulcerans", "Mycobacterium ulcerans Infections", "Infections, Mycobacterium ulcerans", "Infection due to Mycobacterium ulcerans", "Skin infection by Mycobacterium ulcerans", "Mycobacterium ulcerans infectious disease", "cutaneous Mycobacterium ulcerans infection", "Cutaneous mycobacterium ulcerans infection", "Mycobacterium ulcerans disease or disorder", "Mycobacterium ulcerans caused disease or disorder", "cutaneous Mycobacterium ulcerans infection (diagnosis)", "cutaneous M. ulcerans atypical mycobacterial infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Buruli ulcer disease", "shortest_name_length": 11}
{"curie": "UMLS:C2347507", "names": ["Philadelphia-Positive ALL", "Philadelphia Positive Childhood Acute Lymphoblastic Leukemia", "Philadelphia Positive Childhood Precursor Lymphoblastic Leukemia", "B Acute Lymphoblastic Leukemia with t(9;22)(q34.1;q11.2); BCR-ABL1", "Philadelphia chromosome positive childhood acute lymphoblastic leukemia", "Childhood B Acute Lymphoblastic Leukemia with t(9;22)(q34;q11.2); BCR-ABL1", "Childhood B Acute Lymphoblastic Leukemia with t(9;22)(q34.1;q11.2); BCR-ABL1", "Childhood B-Cell Acute Lymphoblastic Leukemia with t(9;22)(q34;q11.2); BCR-ABL1", "Philadelphia chromosome positive childhood precursor acute lymphoblastic leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood B Acute Lymphoblastic Leukemia with t(9;22)(q34.1;q11.2); BCR-ABL1", "shortest_name_length": 25}
{"curie": "MONDO:0030982", "names": ["SQORD", "sulfide quinone oxidoreductase deficiency", "SULFIDE:QUINONE OXIDOREDUCTASE DEFICIENCY", "sulfide:quinone oxidoreductase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sulfide quinone oxidoreductase deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0014892", "names": ["MRD44", "MEBAS", "mercer-Ba syndrome", "autosomal dominant mental retardation 44", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 44", "mental retardation, autosomal dominant 44", "autosomal dominant intellectual disability 44", "intellectual disability, autosomal dominant 44", "autosomal dominant intellectual developmental disorder 44", "autosomal dominant non-syndromic intellectual disability 44", "autosomal dominant intellectual developmental disorder 44 with microcephaly", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 44, WITH MICROCEPHALY", "intellectual developmental disorder, autosomal dominant 44, with microcephaly", "micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0032526", "names": ["SCA48", "SPINOCEREBELLAR ATAXIA 48", "cerebellar ataxia type 48", "spinocerebellar ataxia 48"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia 48", "shortest_name_length": 5}
{"curie": "MONDO:0003243", "names": ["Liver Cell Clear Cell Carcinoma", "liver cell clear cell carcinoma", "clear cell hepatocellular cancer", "Clear Cell Hepatocellular Cancer", "Hepatocellular Clear Cell Carcinoma", "Clear Cell Carcinoma of Liver Cells", "clear cell hepatocellular carcinoma", "hepatocellular clear cell carcinoma", "Clear Cell Hepatocellular Carcinoma", "clear cell carcinoma of liver cells", "Clear Cell Carcinoma of the Liver Cells", "clear cell carcinoma of the liver cells", "Clear cell carcinoma of the Liver cells", "Hepatocellular carcinoma, clear cell type", "clear cell hepatocellular carcinoma of liver", "clear cell hepatocellular carcinoma of liver (diagnosis)", "Hepatocellular carcinoma, clear cell type (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatocellular clear cell carcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C5557308", "names": ["Recurrent Metastatic Gastric Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Metastatic Gastric Carcinoma", "shortest_name_length": 38}
{"curie": "UMLS:C0919884", "names": ["Arterial restenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arterial restenosis", "shortest_name_length": 19}
{"curie": "UMLS:C0152247", "names": ["Urethral Caruncle", "urethral caruncle", "Urethral caruncle", "Caruncle urethral", "Caruncle;urethral", "caruncle; urethral", "urethral; caruncle", "caruncles urethral", "Urethral caruncle (disorder)", "urethral caruncle (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urethral caruncle", "shortest_name_length": 17}
{"curie": "MONDO:0030281", "names": ["AMC6", "ARTHROGRYPOSIS MULTIPLEX CONGENITA 6", "arthrogryposis multiplex congenita 6", "arthrogryposis multiplex congenita-6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis multiplex congenita 6", "shortest_name_length": 4}
{"curie": "MONDO:0019465", "names": ["NMZL", "Monocytoid B-cell lymphoma", "Monocytoid B-Cell Lymphoma", "monocytoid B-cell lymphoma", "monocytoid B-cell; lymphoma", "lymphoma; monocytoid B-cell", "Nodal marginal zone lymphoma", "Nodal Marginal Zone Lymphoma", "B-cell; lymphoma, monocytoid", "nodal marginal zone lymphoma", "lymphoma; B-cell, monocytoid", "Nodal marginal zone B-cell lymph.", "nodal marginal zone B-cell lymph.", "Nodal marginal zone B-cell lymphoma", "nodal marginal zone B-cell lymphoma", "Nodal Marginal Zone B-Cell Lymphoma", "Nodal marginal zone B-cell lymphomas", "Monocytoid B-cell lymphoma (disorder)", "Monocytoid B-cell lymphoma (diagnosis)", "Nodal marginal zone B-cell lymphoma NOS", "Nodal marginal zone B-cell lymphoma (disorder)", "nodal marginal zone B-cell lymphoma (diagnosis)", "Nodal marginal zone B-cell lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nodal marginal zone B-cell lymphoma", "shortest_name_length": 4}
{"curie": "MONDO:0018143", "names": ["pyruvate carboxylase deficiency type C", "pyruvate carboxylase deficiency, benign type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyruvate carboxylase deficiency, benign type", "shortest_name_length": 38}
{"curie": "UMLS:C4289821", "names": ["Cervical Adenocarcinoma Admixed with Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Adenocarcinoma Admixed with Neuroendocrine Carcinoma", "shortest_name_length": 61}
{"curie": "MONDO:0007891", "names": ["lentiginosis profusa", "LENTIGINOSIS PROFUSA", "Lentiginosis Profusa", "Lentiginosis, Diffuse", "LENTIGINOSIS, DIFFUSE", "lentiginosis, diffuse", "LENTIGINOSIS, GENERALIZED", "Lentiginosis, generalized", "Lentiginosis, Generalized", "lentiginosis, generalized", "Familial lentigines profusa", "familial lentigines profusa", "LENTIGINOSIS, INHERITED PATTERNED", "Familial generalized lentiginosis", "lentiginosis, inherited patterned", "Familial generalised lentiginosis", "Lentiginosis, Inherited Patterned", "familial generalized lentiginosis", "Familial generalized lentiginosis (disorder)", "familial multiple lentigines syndrome without systemic involvement", "Familial multiple lentigines syndrome without systemic involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial generalized lentiginosis", "shortest_name_length": 20}
{"curie": "UMLS:C1333855", "names": ["Grade 3 Colon Adenocarcinoma", "Grade III Colon Adenocarcinoma", "Poorly Differentiated Colon Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade 3 Colon Adenocarcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0018015", "names": ["Intermittent hydrarthrosis", "intermittent hydrarthrosis", "intermittent; hydrarthrosis", "hydrarthrosis; intermittent", "Intermittent joint effusion", "HYDRARTHROSIS, INTERMITTENT", "Intermittent effusion of joint", "intermittent hydrarthrosis (diagnosis)", "Intermittent effusion of joint (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intermittent hydrarthrosis", "shortest_name_length": 26}
{"curie": "UMLS:C4553572", "names": ["Stage III Prostate Cancer", "Stage III Prostate Cancer AJCC v8", "Stage III Prostate Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Prostate Cancer AJCC v8", "shortest_name_length": 25}
{"curie": "MONDO:0018247", "names": ["CADDS", "contiguous ABCD1 DXS1357E deletion syndrome", "Zellweger-like contiguous gene deletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CADDS", "shortest_name_length": 5}
{"curie": "UMLS:C0751622", "names": ["L-Tryptophan-Related Eosinophilia-Myalgia Syndrome", "Syndrome, L-Tryptophan-Related Eosinophilia-Myalgia", "Eosinophilia-Myalgia Syndrome, L-Tryptophan-Related", "L-Tryptophan-Related Eosinophilia-Myalgia Syndromes", "Eosinophilia-Myalgia Syndromes, L-Tryptophan-Related", "Syndromes, L-Tryptophan-Related Eosinophilia-Myalgia", "Syndrome, Eosinophilia-Myalgia, L-Tryptophan-Related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eosinophilia-Myalgia Syndrome, L-Tryptophan-Related", "shortest_name_length": 50}
{"curie": "UMLS:C3897750", "names": ["Recurrent Gliosarcoma", "Recurrent Childhood Gliosarcoma", "recurrent childhood gliosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Gliosarcoma", "shortest_name_length": 21}
{"curie": "UMLS:C4049507", "names": ["Relapsed Urothelial Cancer", "Recurrent Urothelial Cancer", "Relapsed Urothelial Carcinoma", "Recurrent Urothelial Carcinoma", "Urothelial carcinoma recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urothelial carcinoma recurrent", "shortest_name_length": 26}
{"curie": "UMLS:C0411065", "names": ["Brachial Plexus Palsy Related to Birth", "Brachial plexus palsy due to birth trauma", "Brachial Plexus Palsy due to Birth Trauma", "Brachial plexus palsy due to birth trauma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brachial plexus palsy due to birth trauma", "shortest_name_length": 38}
{"curie": "UMLS:C0852878", "names": ["Non-accidental injury", "non-accidental injury", "Non-accidental injury (disorder)", "Non-accidental injury (diagnosis)", "injuries / accidents non-accidental injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-accidental injury", "shortest_name_length": 21}
{"curie": "MONDO:0013649", "names": ["Hypt9", "HYPT9", "hypt9", "hypotrichosis 9", "HYPOTRICHOSIS 9", "hypotrichosis type 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotrichosis 9", "shortest_name_length": 5}
{"curie": "UMLS:C5206657", "names": ["Penile Mesenchymal Neoplasm", "Penile Soft Tissue Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Penile Soft Tissue Neoplasm", "shortest_name_length": 27}
{"curie": "MONDO:0009064", "names": ["ocular cystinosis", "Ocular cystinosis", "Adult-onset cystinosis", "adult-onset cystinosis", "non-nephropathic cystinosis", "Non-nephropathic cystinosis", "Ocular nonnephropathic cystinosis", "Cystinosis, Adult Nonnephropathic", "cystinosis, ADULT NONNEPHROPATHIC", "CYSTINOSIS, ADULT NONNEPHROPATHIC", "Cystinosis, ocular nonnephropathic", "cystinosis, benign Nonnephropathic", "CYSTINOSIS, OCULAR NONNEPHROPATHIC", "cystinosis, ocular Nonnephropathic", "Cystinosis, adult, nonnephropathic", "CYSTINOSIS, BENIGN NONNEPHROPATHIC", "Cystinosis, Benign Nonnephropathic", "Cystinosis, benign, nonnephropathic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ocular cystinosis", "shortest_name_length": 17}
{"curie": "UMLS:C4520740", "names": ["stage II salivary gland cancer", "Stage II Salivary Gland Cancer", "Stage II Salivary Gland Carcinoma", "Stage II Major Salivary Gland Cancer", "Stage II Major Salivary Gland Carcinoma", "Stage II Carcinoma of Major Salivary Gland", "Stage II Major Salivary Gland Cancer AJCC v7", "Stage II Carcinoma of the Major Salivary Gland", "Stage II Major Salivary Gland Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Major Salivary Gland Cancer AJCC v7", "shortest_name_length": 30}
{"curie": "MONDO:0012130", "names": ["MFM2", "myofibrillar myopathy 2", "alpha-B crystallinopathy", "alpha-b crystallinopathy", "Alpha-B Crystallinopathy", "ALPHA-B CRYSTALLINOPATHY", "MYOPATHY, MYOFIBRILLAR, 2", "myopathy, myofibrillar, 2", "myofibrillar myopathy type 2", "myopathy, myofibrillar, type 2", "late-onset distal crystallinopathy", "CRYAB autosomal dominant distal myopathy", "MYOPATHY, MYOFIBRILLAR, ALPHA-B CRYSTALLIN-RELATED", "Myopathy, Myofibrillar, Alpha-B Crystallin-Related", "myopathy, myofibrillar, alpha-B crystallin-related", "alpha-B crystallin-related late-onset distal myopathy", "Myopathy, Cardioskeletal, Desmin-Related, with Cataract", "autosomal dominant distal myopathy caused by mutation in CRYAB", "myopathy, desmin-related, associated with mutation in the Cryab Gene", "Myopathy, Desmin-Related, associated with Mutation in the CRYAB Gene", "MYOPATHY, DESMIN-RELATED, ASSOCIATED WITH MUTATION IN THE CRYAB GENE", "myopathy, myofibrillar, with or without cataract and/or cardiomyopathy", "MYOPATHY, MYOFIBRILLAR, WITH OR WITHOUT CATARACT AND/OR CARDIOMYOPATHY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myofibrillar myopathy 2", "shortest_name_length": 4}
{"curie": "MONDO:0021055", "names": ["fap", "APC", "FAP", "FPC", "FAP1", "classic FAP", "adenomatosis", "Adenomatosis", "polyposis coli", "Polyposis Coli", "Polyposis coli", "Coli, Polyposis", "Polyposis Colus", "Colus, Polyposis", "polyposis; colon", "Adenomatosis, NOS", "familial polyposis", "polyposis familial", "FAMILIAL POLYPOSIS", "Familial polyposis", "Multiple polyposis", "COLON NOS POLYPOSIS", "familial; polyposis", "polyposis; familial", "Adenomatous polyposis", "adenomatous polyposis", "colon; polyposis coli", "familial polyposis coli", "Familial Polyposis Coli", "Familial polyposis coli", "Myh Associated Polyposis", "Myh-Associated Polyposes", "Familial Polyposis Colus", "Coli, Familial Polyposis", "MYH-associated polyposis", "Polyposis Coli, Familial", "Myh-Associated Polyposis", "hereditary polyposis coli", "Polyposes, Myh-Associated", "Hereditary Polyposis Coli", "polyposis, MYH-associated", "Colus, Familial Polyposis", "Polyposis, Myh-Associated", "Polyposis Colus, Familial", "Familial Multiple Polyposi", "Coli, Hereditary Polyposis", "POLYP ADENOMATOUS MULTIPLE", "Adenomatous Polyposis Coli", "adenomatous polyposis coli", "Adenomatous polyposis coli", "adenomatous coli polyposis", "Hereditary Polyposis Colus", "Polyposis Coli, Hereditary", "[M]Familial polyposis coli", "Polyposis Colus, Hereditary", "Familial Multiple Polyposis", "Polyposis Coli, Adenomatous", "Familial Polyposis Syndrome", "familial polyposis syndrome", "Coli, Adenomatous Polyposis", "Multiple Adenomatous Polyps", "Polyposi, Familial Multiple", "Familial Multiple Polyposes", "Multiple adenomatous polyps", "Familial Multiple Polyposus", "Multiple Polyposi, Familial", "Colus, Hereditary Polyposis", "Adenomatous Polyposis Colus", "familial multiple polyposis", "Familial Polyposis Syndromes", "Colus, Adenomatous Polyposis", "Polyposis Colus, Adenomatous", "Polyposis, Familial Multiple", "Multiple Polyposus, Familial", "Polyposus, Familial Multiple", "Polyposis Syndrome, Familial", "Polyposes, Familial Multiple", "Multiple Polyposes, Familial", "Multiple Polyposis, Familial", "[M]Adenomatous polyposis coli", "familial intestinal polyposis", "Adenomatous colonic polyposis", "FPC - Familial polyposis coli", "Familial Adenomatous Polyposis", "Familial Adenomatous Polyposes", "MAP - MYH associated polyposis", "adenomatosis; unspecified site", "familial adenomatous polyposis", "Familial adenomatous polyposis", "Familial Polyposis of the Colon", "Adenomatous Polyposis, Familial", "FAMILIAL POLYPOSIS OF THE COLON", "Adenomatous Polyposes, Familial", "Polyposis, Familial Adenomatous", "Polyposes, Familial Adenomatous", "polyposis, familial adenomatous", "FAMILIAL ADENOMATOUS POLYPOSIS 1", "APC - adenomatous polyposis coli", "Colorectal adenomatous polyposis", "APC - Adenomatous polyposis coli", "Familial Adenomatous Polyposis 1", "APC - Adenomatous Polyposis Coli", "colorectal adenomatous polyposis", "Multiple adenomatous colon polyps", "Adenomatous Polyposis of the Colon", "ADENOMATOUS POLYPOSIS OF THE COLON", "adenomatous polyposis of the colon", "Multiple colonic adenomatous polyps", "MYH-associated polyposis (disorder)", "familial adenomatous polyposis coli", "Familial Adenomatous Polyposis Coli", "FAP (familial adenomatous polyposis)", "Adenomatous Polyposis Coli, Familial", "Familial multiple polyposis syndrome", "FAP - Familial adenomatous polyposis", "Familial Multiple Polyposis Syndrome", "GI Tract Multiple Adenomatous Polyps", "Hereditary Adenomatous Polyposis Coli", "hereditary adenomatous polyposis coli", "classic familial adenomatous polyposis", "COLON, POLYPOSIS, FAMILIAL ADENOMATOUS", "familial adenomatous polyposis syndrome", "Familial Adenomatous Polyposis Syndrome", "Familial Adenomatous Polyposis of the Colon", "familial adenomatous polyposis of the colon", "adenomatous polyposis coli of large intestine", "Familial multiple polyposis syndrome (disorder)", "Gastrointestinal Tract Multiple Adenomatous Polyps", "Adenomatous polyposis coli (morphologic abnormality)", "Multiple adenomatous polyps (morphologic abnormality)", "adenomatous polyposis coli of large intestine (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "classic familial adenomatous polyposis", "shortest_name_length": 3}
{"curie": "MONDO:0010425", "names": ["LECD", "LISCH EPITHELIAL CORNEAL DYSTROPHY", "Lisch Epithelial Corneal Dystrophy", "Lisch epithelial corneal dystrophy", "CORNEAL DYSTROPHY, LISCH EPITHELIAL", "Corneal Dystrophy, Lisch Epithelial", "band-shaped and whorled microcystic", "corneal dystrophy, Lisch epithelial", "Lisch epithelial corneal dystrophy (disorder)", "corneal dystrophy, Lisch epithelial, X-linked dominant", "band-Shaped and whorled microcystic corneal epithelial dystrophy", "Band-Shaped And Whorled Microcystic Corneal Epithelial Dystrophy", "BAND-SHAPED AND WHORLED MICROCYSTIC CORNEAL EPITHELIAL DYSTROPHY", "Band-shaped and whorled microcystic dystrophy of corneal epithelium", "band-shaped and whorled microcystic dystrophy of the corneal epithelium", "Band-shaped and whorled microcystic dystrophy of the corneal epithelium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lisch epithelial corneal dystrophy", "shortest_name_length": 4}
{"curie": "UMLS:C0031315", "names": ["Pseudomelia", "Phantom pain", "Phantom limb", "Pseudomelias", "phantom limb", "Phantom Limb", "pain phantom", "limb phantom", "phantom pain", "Phantom Limbs", "Limb, Phantom", "limbs phantom", "phantom limbs", "pains phantom", "Limbs, Phantom", "phantom limb pain", "Phantom Sensation", "Phantom Limb Pain", "limb pain phantom", "PHANTOM LIMB PAIN", "Phantom limb pain", "Phantom Sensations", "limb pains phantom", "Sensation, Phantom", "Stump Hallucination", "Stump hallucination", "Sensations, Phantom", "Phantom limb syndrome", "phantom limb syndrome", "Phantom Limb Syndrome", "phantom limb; syndrome", "syndrome; phantom limb", "Phantom limb (syndrome)", "Phantom limb (disorder)", "Phantom limb syndrome NOS", "PLS - Phantom limb syndrome", "pain; phantom limb syndrome", "phantom limb syndrome; pain", "FLS - Phantom limb syndrome", "Phantom limb syndrome with pain", "phantom limb syndrome with pain", "phantom limb syndrome (diagnosis)", "phantom limb; syndrome, with pain", "syndrome; phantom limb, with pain", "phantom limb syndrome with pain (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Phantom Limb Syndrome", "shortest_name_length": 11}
{"curie": "UMLS:C0877126", "names": ["Application site inflammation", "Application site inflammation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Application site inflammation", "shortest_name_length": 29}
{"curie": "UMLS:C0268912", "names": ["Vas Deferens Hemorrhage", "Vas deferens hemorrhage", "Vas deferens haemorrhage", "vas deferens; hemorrhage", "hemorrhage; vas deferens", "hemorrhage of vas deferens", "Hemorrhage of vas deferens", "Haemorrhage of vas deferens", "Hemorrhage of vas deferens (disorder)", "hemorrhage of vas deferens (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemorrhage of vas deferens", "shortest_name_length": 23}
{"curie": "MONDO:0005783", "names": ["HEMOPERICARDIUM", "Hemopericardium", "hemopericardium", "haemopericardium", "Haemopericardium", "Hematopericardium", "Haematopericardium", "Pericardial bleeding", "Hemorrhage pericardial", "Pericardial hemorrhage", "HEMORRHAGE PERICARDIAL", "hemorrhage; pericardium", "Pericardial haemorrhage", "pericardium; hemorrhage", "Haemorrhage pericardial", "hemopericardium (disease)", "Hemopericardium (disorder)", "hemopericardium (diagnosis)", "HEMORRHAGE INTRAPERICARDIAL", "Hemorrhage intrapericardial", "Haemorrhage intrapericardial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemopericardium", "shortest_name_length": 15}
{"curie": "UMLS:C5447549", "names": ["Refractory Giant Cell Glioblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Giant Cell Glioblastoma", "shortest_name_length": 34}
{"curie": "UMLS:C5237431", "names": ["Diffuse Large B-Cell Lymphoma with Associated Monoclonal Small B-Cell Population in Bone Marrow"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse Large B-Cell Lymphoma with Associated Monoclonal Small B-Cell Population in Bone Marrow", "shortest_name_length": 95}
{"curie": "MONDO:0016560", "names": ["ptosis-syndactyly-learning difficulties syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ptosis-syndactyly-learning difficulties syndrome", "shortest_name_length": 48}
{"curie": "MONDO:0026727", "names": ["SHUVER", "SHUKLA-VERNON SYNDROME", "Shukla-Vernon syndrome", "Shukla-Vernon syndrome, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Shukla-Vernon syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C0877306", "names": ["Iris hyperpigmentation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Iris hyperpigmentation", "shortest_name_length": 22}
{"curie": "MONDO:0017467", "names": ["Tibio-fibular fusion", "tibio-fibular synostosis", "Tibio-fibular synostosis", "Congenital tibio-fibular fusion", "Tibio-fibular synostosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tibio-fibular synostosis", "shortest_name_length": 20}
{"curie": "UMLS:C3541293", "names": ["Systemic Arterial Hypertensive Disorder", "Hypertensive Disorder, Systemic Arterial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Systemic Arterial Hypertensive Disorder", "shortest_name_length": 39}
{"curie": "MONDO:0013056", "names": ["DEE39", "EIEE39", "AGC1 DEFICIENCY", "AGC1 Deficiency", "AGC1 deficiency", "hypomyelination, global cerebral", "Hypomyelination, Global Cerebral", "HYPOMYELINATION, GLOBAL CEREBRAL", "aspartate-glutamate carrier 1 deficiency", "ASPARTATE-GLUTAMATE CARRIER 1 DEFICIENCY", "Aspartate-Glutamate Carrier 1 Deficiency", "early infantile epileptic encephalopathy 39", "epileptic encephalopathy, early infantile, 39", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 39", "developmental and epileptic encephalopathy 39", "developmental and epileptic encephalopathy, 39", "SLC25A12 early infantile epileptic encephalopathy", "mitochondrial aspartate-glutamate carrier 1 deficiency", "Mitochondrial aspartate-glutamate carrier 1 deficiency", "epileptic encephalopathy with global cerebral demyelination", "Epileptic encephalopathy with global cerebral demyelination", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 39 WITH LEUKODYSTROPHY", "Epileptic encephalopathy with global cerebral demyelination (disorder)", "early infantile epileptic encephalopathy caused by mutation in SLC25A12", "Epileptic encephalopathy with global cerebral demyelination (diagnosis)", "epilepsy generalized epileptic encephalopathy with global cerebral demyelination"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 39", "shortest_name_length": 5}
{"curie": "UMLS:C4727392", "names": ["Recurrent Salivary Duct Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Salivary Duct Carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0019405", "names": ["FOSMN syndrome", "facial onset sensory and motor neuronopathy", "Facial onset sensory and motor neuronopathy", "facial onset sensorimotor neuronopathy syndrome", "facial onset sensory and motor neuronopathy syndrome", "Facial onset sensory and motor neuronopathy syndrome", "FOSMN (facial onset sensory and motor neuronopathy) syndrome", "Facial onset sensory and motor neuronopathy syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "facial onset sensory and motor neuronopathy", "shortest_name_length": 14}
{"curie": "UMLS:C0948231", "names": ["Lip erosion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lip erosion", "shortest_name_length": 11}
{"curie": "MONDO:0007004", "names": ["Type III reaction", "Immune Complex Disease", "Immune complex disease", "immune complex disease", "Immune Complex Diseases", "Disease, Immune Complex", "immune complex diseases", "Immune complex diseases", "Diseases, Immune Complex", "type iii hypersensitivity", "type III hypersensitivity", "Type III Hypersensitivity", "hypersensitivity iii type", "Hypersensitivity, Type III", "Type III Hypersensitivities", "Hypersensitivities, Type III", "Type 3 hypersensitivity reaction", "type 3 hypersensitivity reaction", "Type 3 Hypersensitivity Reaction", "type III hypersensitivity disease", "Gell and Coombs reaction type III", "Immune complex formation syndrome", "Hypersensitivity reaction type III", "type III hypersensitivity reaction", "Type III hypersensitivity reaction", "Type III Hypersensitivity Reaction", "Type III reaction (Gell and Coombs)", "disorder of type III hypersensitivity", "hypersensitivity reaction type III disease", "type III hypersensitivity reaction disease", "Hypersensitivity reaction mediated by immune complex", "Hypersensitivity reaction mediated by immune complex (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type III hypersensitivity disease", "shortest_name_length": 17}
{"curie": "MONDO:0010091", "names": ["CISS", "CISS1", "CRISPONI SYNDROME", "Crisponi Syndrome", "Crisponi syndrome", "Sweating, cold-induced", "Sohar-Crisponi syndrome", "SOHAR-CRISPONI SYNDROME", "Sohar-Crisponi Syndrome", "Crisponi syndrome (disorder)", "Cold-induced sweating syndrome", "CNTF receptor-related disorders", "Cold-induced sweating syndrome 1", "cold-induced sweating syndrome 1", "Cold-Induced Sweating Syndrome 1", "COLD-INDUCED SWEATING SYNDROME 1", "cold-induced sweating syndrome type 1", "Cold-induced sweating syndrome (disorder)", "CRISPONI/cold-induced sweating syndrome 1", "Crisponi/Cold-Induced Sweating Syndrome-1", "Crisponi/cold-induced sweating syndrome 1", "CRISPONI/COLD-INDUCED SWEATING SYNDROME 1", "Ciliary neurotrophic factor receptor-related disorder", "MUSCLE CONTRACTIONS, TETANOFORM, WITH CHARACTERISTIC FACE, CAMPTODACTYLY, HYPERTHERMIA, AND SUDDEN DEATH", "muscle contractions, Tetanoform, with characteristic face, camptodactyly, hyperthermia, and sudden death"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cold-induced sweating syndrome 1", "shortest_name_length": 4}
{"curie": "MONDO:0001665", "names": ["Ophthalmic tularemia", "OPHTHALMIC TULAREMIA", "tularemia; ophthalmic", "ophthalmic; tularemia", "oculoglandular tularemia", "Oculoglandular tularemia", "CONJUNCTIVITIS, TULAREMIC", "Oculoglandular tularaemia", "tularemia; oculoglandular", "oculoglandular; tularemia", "Oculoglandular tularemia (disorder)", "oculoglandular tularemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculoglandular tularemia", "shortest_name_length": 20}
{"curie": "UMLS:C1708486", "names": ["Incisional Burn"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Incisional Burn", "shortest_name_length": 15}
{"curie": "MONDO:0010025", "names": ["SSOS", "Short Stature-Obesity Syndrome", "SHORT STATURE-OBESITY SYNDROME", "short stature-obesity syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short stature-obesity syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0280173", "names": ["Stage IV Diffuse Small Cleaved Cell Lymphoma", "Stage IV Adult Diffuse Small Cleaved Cell Lymphoma", "Adult Diffuse Small Cleaved Cell Lymphoma Stage IV", "stage IV adult diffuse small cleaved cell lymphoma", "adult diffuse small cleaved cell lymphoma, stage IV", "metastatic adult diffuse small cleaved cell lymphoma", "adult diffuse small cleaved cell lymphoma, metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Adult Diffuse Small Cleaved Cell Lymphoma", "shortest_name_length": 44}
{"curie": "MONDO:0003050", "names": ["LCLC", "large cell cancer lung", "large cell lung cancer", "LUNG CANCER LARGE CELL", "Large cell lung cancer", "lung cancer large cell", "Large Cell Lung Cancer", "lung cancer, large cell", "cancer cells large lung", "Lung Large Cell Carcinoma", "large cell lung carcinoma", "large cell carcinoma lung", "carcinoma cell large lung", "Large cell lung carcinoma", "lung large cell carcinoma", "Large Cell Lung Carcinoma", "Anaplastic Lung Carcinoma", "anaplastic lung carcinoma", "carcinoma cell large lungs", "anaplastic carcinoma of lung", "large cell carcinoma of lung", "Large cell carcinoma of lung", "Large Cell Carcinoma of Lung", "Large Cell Carcinoma of the Lung", "large cell carcinoma of the lung", "anaplastic large cell lung cancer", "lung cancer, anaplastic large cell", "Large cell carcinoma of lung (disorder)", "undifferentiated large cell lung cancer", "lung cancer, undifferentiated large cell", "large cell carcinoma of lung (diagnosis)", "anaplastic carcinoma of lung (diagnosis)", "large cell undifferentiated lung carcinoma", "Large Cell Undifferentiated Lung Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung large cell carcinoma", "shortest_name_length": 4}
{"curie": "UMLS:C4721412", "names": ["Malignant insulinoma", "Malignant Insulinoma", "Insulinoma, malignant", "Malignant beta cell tumor", "Malignant beta cell tumour", "Beta-cell tumor, malignant", "Beta cell tumor, malignant", "Beta cell tumour, malignant", "insulin producing carcinoma", "insulin secreting carcinoma", "Malignant Pancreatic Insulinoma", "Malignant insulinoma (disorder)", "pancreatic beta islet cell carcinoma", "Pancreatic Beta Islet Cell Carcinoma", "carcinoma, pancreatic beta islet cell", "beta islet cell carcinoma, pancreatic", "Pancreatic Insulin Producing Carcinoma", "islet cell, beta, pancreatic carcinoma", "Insulinoma, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Pancreatic Insulinoma", "shortest_name_length": 20}
{"curie": "UMLS:C2981706", "names": ["IIA", "Stage IIA Uveal Melanoma", "Stage IIA Uveal Melanoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Uveal Melanoma AJCC v7", "shortest_name_length": 3}
{"curie": "MONDO:0001768", "names": ["lacrimal passages; stenosis", "Stenosis of lacrimal passage", "stenosis of lacrimal passage", "Stenosis of lacrimal canaliculi", "stenosis of lacrimal canaliculi", "Stenosis of lacrimal canaliculus", "Stenosis of lacrimal canaliculi (disorder)", "Stenosis of unspecified lacrimal canaliculi", "stenosis of lacrimal canaliculi (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stenosis of lacrimal passage", "shortest_name_length": 27}
{"curie": "MONDO:0013263", "names": ["RP54", "retinitis pigmentosa 54", "RETINITIS PIGMENTOSA 54", "PCARE retinitis pigmentosa", "retinitis pigmentosa type 54", "retinitis pigmentosa caused by mutation in PCARE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 54", "shortest_name_length": 4}
{"curie": "UMLS:C1290384", "names": ["Structural disorder of heart", "heart disease structural disorder", "Structural disorder of heart (disorder)", "Structural disorder of heart (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Structural disorder of heart", "shortest_name_length": 28}
{"curie": "MONDO:0019466", "names": ["AIL", "LYG", "Lymphoid granulomatosis", "granulomatosis; lymphoid", "lymphoid; granulomatosis", "lymphomatoid granulomatosis", "Lymphomatoid granulomatosis", "Lymphomatoid Granulomatosis", "Lymphomatoid Granulomatoses", "LYMPHOMATOID GRANULOMATOSIS", "Granulomatosis, Lymphomatoid", "Granulomatoses, Lymphomatoid", "LG - Lymphomatoid granulomatosis", "Lymphomatoid granulomatosis (disorder)", "Angiocentric Immunoproliferative Lesion", "Angiocentric immunoproliferative lesion", "lymphomatoid granulomatosis (diagnosis)", "angiocentric immunoproliferative; lesion", "lesion; angiocentric immunoproliferative", "lymphomatoid granulomatosis (grades I and II)", "Lymphomatoid granulomatosis (morphologic abnormality)", "Angiocentric immunoproliferative lesion (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphomatoid granulomatosis", "shortest_name_length": 3}
{"curie": "MONDO:0021574", "names": ["OOMD3", "OOCYTE MATURATION DEFECT 3", "oocyte maturation defect 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oocyte maturation defect 3", "shortest_name_length": 5}
{"curie": "MONDO:0008270", "names": ["TPT", "PPD2", "TPTPS", "TPT-PS SYNDROME", "TPT-PS syndrome", "Finger-like thumb", "Digitalized thumb", "Thumbs digitalized", "Finger-like thumbs", "TRIPHALANGEAL THUMB", "Thumbs, digitalized", "Triphalangeal Thumb", "triphalangeal thumb", "Triphalangeal thumb", "TPT and PSD syndrome", "Triphalangeal thumbs", "thumbs triphalangeal", "THUMB, TRIPHALANGEAL", "Triphalangy of thumb", "triphalangeal thumbs", "Triphalangeal thumb(s)", "polydactyly, preaxial 2", "POLYDACTYLY, PREAXIAL II", "polydactyly, preaxial II", "Polydactyly, Preaxial II", "preaxial polydactyly type 2", "triphalangeal thumb, type i", "Preaxial polydactyly type 2", "Patterson Stevenson syndrome", "polydactyly, preaxial type 2", "polydactyly, preaxial type II", "Triphalangeal thumb (disorder)", "Accessory phalanx of the thumb", "polydactyly of triphalangeal thumb", "POLYDACTYLY OF TRIPHALANGEAL THUMB", "Polydactyly of triphalangeal thumb", "Polydactyly of Triphalangeal Thumb", "polydactyly of a triphalangeal thumb", "Polydactyly of a triphalangeal thumb", "Patterson-Stevenson-Fontaine Syndrome", "Patterson Stevenson Fontaine syndrome", "triphalangeal thumbs (physical finding)", "Triphalangeal Thumb with Polysyndactyly", "TRIPHALANGEAL THUMB WITH POLYSYNDACTYLY", "triphalangeal thumb with polysyndactyly", "Triphalangeal Thumb-Polydactyly Syndrome", "triphalangeal thumb-polydactyly syndrome", "TRIPHALANGEAL THUMB-POLYDACTYLY SYNDROME", "TRIPHALANGEAL THUMB-POLYSYNDACTYLY SYNDROME", "Triphalangeal thumb polysyndactyly syndrome", "triphalangeal thumb-polysyndactyly syndrome", "Triphalangeal Thumb-Polysyndactyly Syndrome", "Polydactyly of triphalangeal thumb (disorder)", "Triphalangeal thumb and polysyndactyly syndrome", "Split-Foot Deformity With Mandibulofacial Dysostosis", "Triphalangeal thumb and polysyndactyly syndrome (disorder)", "Split-foot deformity with ectrodactyly and mandibulofacial dysostosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polydactyly of a triphalangeal thumb", "shortest_name_length": 3}
{"curie": "UMLS:C4521787", "names": ["IIA", "Stage IIA Gastric (Stomach) Cancer", "Pathologic Stage IIA Gastric Cancer AJCC v8", "Pathologic Stage IIA Gastric Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IIA Gastric Cancer AJCC v8", "shortest_name_length": 3}
{"curie": "UMLS:C0426015", "names": ["uterine scar", "Uterine scar", "uterus; scar", "scar; uterus", "scars uterus", "scarred uterus", "uterus scarring", "uterus; cicatrix", "Scarring of uterus", "scarring of uterus", "uterine scar (diagnosis)", "Scarring of uterus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Scarring of uterus", "shortest_name_length": 12}
{"curie": "MONDO:0012598", "names": ["HGF4", "GGF4", "GINGF4", "gingival fibromatosis, 4", "Fibromatosis, Gingival, 4", "FIBROMATOSIS, GINGIVAL, 4", "fibromatosis, gingival, 4", "hereditary gingival fibromatosis, 4", "fibromatosis gingival, hereditary, 4", "fibromatosis, gingival, hereditary, 4", "Fibromatosis, Gingival, Hereditary, 4", "FIBROMATOSIS, GINGIVAL, HEREDITARY, 4", "FIBROMATOSIS, GINGIVAL, HEREDITARY, 4 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibromatosis, gingival, 4", "shortest_name_length": 4}
{"curie": "MONDO:0056803", "names": ["sulfur metabolism disease", "Disorder of sulfur metabolism", "disorder of sulfur metabolism", "Disorder of sulphur metabolism", "disorder of sulphur metabolism", "disorder of sulfur metabolic process", "Disorder of sulfur metabolism (disorder)", "sulfur compound metabolic process disease", "disorder of sulfur compound metabolic process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sulfur metabolism disease", "shortest_name_length": 25}
{"curie": "UMLS:C1845837", "names": ["Gata1-Related Cytopenia", "GATA 1 related cytopenia", "X linked macrothrombocytopenia", "X-Linked Macrothrombocytopenia", "Gata1-Related X-Linked Cytopenia", "GATA 1 related X linked cytopenia", "Dyserythropoietic Anemia and Thrombocytopenia", "Dyserythropoietic anemia and thrombocytopenia", "Dyserythropoietic Anemia with Thrombocytopenia", "Dyserythropoietic anaemia and thrombocytopaenia", "GATA binding protein 1 related thrombocytopenia with dyserythropoiesis", "GATA binding protein 1 related thrombocytopaenia with dyserythropoiesis", "GATA binding protein 1 related thrombocytopenia with dyserythropoiesis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dyserythropoietic Anemia with Thrombocytopenia", "shortest_name_length": 23}
{"curie": "UMLS:C4744835", "names": ["Recurrent Ovarian Low-Grade Serous Adenocarcinoma", "Recurrent Ovarian Low Grade Serous Adenocarcinoma", "Recurrent Low Grade Ovarian Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Ovarian Low Grade Serous Adenocarcinoma", "shortest_name_length": 49}
{"curie": "MONDO:0021231", "names": ["retina tumor", "Retina Tumor", "retinal tumor", "Retinal Tumor", "Tumor of Retina", "tumor of retina", "retina neoplasm", "Retina Neoplasm", "retinal neoplasm", "Retinal Neoplasm", "Neoplasm of Retina", "neoplasm of retina", "Tumor of the Retina", "tumor of the retina", "neoplasm of the retina", "Neoplasm of the Retina", "retina neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retina neoplasm", "shortest_name_length": 12}
{"curie": "MONDO:0008513", "names": ["SD2a", "SPD1", "Synpolydactyly-1", "synpolydactyly 1", "SYNPOLYDACTYLY 1", "syndactyly, type 2", "SD2, Vordingborg type", "synpolydactyly type 1", "SPD, Vordingborg type", "Synpolydactyly type 1", "synpolydactyly, Vordingborg type", "Synpolydactyly, Vordingborg type", "synpolydactyly with foot anomalies", "HOXD13 non-syndromic synpolydactyly", "non-syndromic synpolydactyly caused by mutation in HOXD13"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "synpolydactyly type 1", "shortest_name_length": 4}
{"curie": "MONDO:0002616", "names": ["mesenchymal tumor", "Mesenchymal Tumor", "Mesenchymal Neoplasm", "mesenchymal neoplasm", "mesenchymal cell tumor", "Mesenchymal Cell Tumor", "mesenchymal cell neoplasm", "Mesenchymal Cell Neoplasm", "benign miscellaneous mesenchymal tumor", "Benign Soft Tissue Tumor of Uncertain Differentiation", "Benign Soft Tissue Neoplasm of Uncertain Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mesenchymal cell neoplasm", "shortest_name_length": 17}
{"curie": "UMLS:C0032787", "names": ["post-op complication", "Complication;post-op", "complications post op", "Postoperative problem", "Postoperative complication", "Postoperative Complication", "postoperative complication", "complication postoperative", "complications postoperative", "Complication, Postoperative", "postoperative complications", "Postoperative Complications", "complications; postoperative", "postoperative; complications", "Complications, Postoperative", "Postoperative complication NOS", "Postoperative complication, NOS", "Postoperative complications NOS", "Postoperative complication (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postoperative Complications", "shortest_name_length": 20}
{"curie": "UMLS:C1608946", "names": ["Hemorrhagic arteriovenous malformation", "Haemorrhagic arteriovenous malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemorrhagic arteriovenous malformation", "shortest_name_length": 38}
{"curie": "MONDO:0000647", "names": ["benign vaginal tumor", "Benign Vaginal Tumor", "Benign vaginal tumor", "Benign vaginal tumour", "benign tumors vaginal", "Benign neoplasm vagina", "Benign tumor of vagina", "benign tumor of vagina", "Benign Tumor of Vagina", "vagina benign neoplasm", "benign vaginal neoplasm", "vaginal benign neoplasm", "Benign tumour of vagina", "Vaginal neoplasm benign", "Benign vaginal neoplasm", "Benign Vaginal Neoplasm", "VAGINAL NEOPLASM BENIGN", "Benign Vaginal Neoplasms", "Vaginal neoplasms benign", "benign vaginal neoplasms", "Benign neoplasm of vagina", "benign neoplasm of vagina", "Benign Neoplasm of Vagina", "Benign Tumor of the Vagina", "benign tumor of the vagina", "benign neoplasm of the vagina", "Benign Neoplasm of the Vagina", "Benign neoplasm of vagina, NOS", "Benign neoplasm of vagina (disorder)", "benign neoplasm of vagina (diagnosis)", "vagina female reproductive organ benign neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign vaginal neoplasm", "shortest_name_length": 20}
{"curie": "UMLS:C3711162", "names": ["Metatropic dysplasia 1", "Metatropic Dysplasia Type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metatropic Dysplasia Type 1", "shortest_name_length": 22}
{"curie": "UMLS:C1864267", "names": ["Endotoxin Hyporesponsiveness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endotoxin Hyporesponsiveness", "shortest_name_length": 28}
{"curie": "UMLS:C0159324", "names": ["MANDIBLE FRACTURE CLOSED", "Mandible closed fracture", "Closed fracture of mandible", "Closed Fracture of Mandible", "closed fracture of mandible", "Fracture of mandible, closed", "Closed fracture of lower jaw", "Fracture of lower jaw, closed", "Closed fracture of mandible, NOS", "Closed fracture of lower jaw bone", "Closed fracture of Inferior maxilla", "Closed fracture of inferior maxilla", "Fracture of mandible, closed (disorder)", "closed fracture of mandible (diagnosis)", "Closed fracture of mandible, unspecified site", "Unspecified site of mandible, closed fracture"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fracture of mandible, closed", "shortest_name_length": 24}
{"curie": "MONDO:0014744", "names": ["SCAR21", "CALFAN", "autosomal recessive spinocerebellar ataxia 21", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 21", "spinocerebellar ataxia, autosomal recessive 21", "autosomal recessive spinocerebellar ataxia type 21", "Autosomal recessive spinocerebellar ataxia type 21", "spinocerebellar ataxia, autosomal recessive type 21", "autosomal recessive spinocerebellar ataxia 21 with hepatopathy", "spinocerebellar ataxia, autosomal recessive 21, with hepatopathy", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 21, WITH HEPATOPATHY", "CHOLESTASIS, LOW GGT, ACUTE LIVER FAILURE, AND NEURODEGENERATION SYNDROME", "Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome", "acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome", "Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome", "Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0006410", "names": ["Simple", "simple endometrial hyperplasia", "Simple endometrial hyperplasia", "Simple Endometrial Hyperplasia", "Endometrial Hyperplasia, Simple", "Simple Endometrial Hyperplasias", "Hyperplasia, Simple Endometrial", "Endometrial Hyperplasias, Simple", "Hyperplasias, Simple Endometrial", "Simple endometrial hyperplasia (disorder)", "simple endometrial hyperplasia (diagnosis)", "Cystic glandular hyperplasia of endometrium", "CGH - Cystic glandular hyperplasia of endometrium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "simple endometrial hyperplasia", "shortest_name_length": 6}
{"curie": "MONDO:0016726", "names": ["neuronal tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuronal tumor", "shortest_name_length": 14}
{"curie": "MONDO:0002918", "names": ["CCM", "Clear cell meningioma", "clear cell meningioma", "Clear Cell Meningioma", "Clear Cell Meningiomas", "Meningioma, Clear Cell", "Meningiomas, Clear Cell", "clear cell meningioma (morphologic abnormality)", "Clear cell meningioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "clear cell meningioma", "shortest_name_length": 3}
{"curie": "MONDO:0001435", "names": ["bullous retinoschisis", "Bullous retinoschisis", "Bullous retinoschisis (disorder)", "bullous retinoschisis (diagnosis)", "Peripheral retinoschisis, retinal cysts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bullous retinoschisis", "shortest_name_length": 21}
{"curie": "MONDO:0005414", "names": ["TRS", "refractory schizophrenia", "treatment-refractory schizophrenia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "treatment-refractory schizophrenia", "shortest_name_length": 3}
{"curie": "MONDO:0004508", "names": ["Apical Periodontitis", "apical periodontitis", "Apical periodontitis", "periodontitis; apical", "Periodontitis, Apical", "Apical Periodontitides", "Periodontitides, Apical", "Apical periodontitis NOS", "Periapical Periodontitis", "periapical periodontitis", "Periapical periodontitis", "Apical periodontitis, NOS", "Periodontitis, Periapical", "Periapical Periodontitides", "Periodontitides, Periapical", "Apical periodontitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "periapical periodontitis", "shortest_name_length": 20}
{"curie": "MONDO:0010710", "names": ["Chitayat Meunier Hodgkinson syndrome", "Chitayat-Meunier-Hodgkinson syndrome", "Pierre Robin syndrome, faciodigital anomaly", "[OBSOLETE] Chitayat Meunier Hodgkinson syndrome", "Robin sequence with facial and digital anomalies", "Pierre Robin sequence faciodigital anomaly syndrome", "Pierre Robin syndrome-faciodigital anomaly syndrome", "Pierre Robin sequence-faciodigital anomaly syndrome", "Pierre Robin Sequence with Facial and Digital Anomalies", "PIERRE ROBIN SEQUENCE WITH FACIAL AND DIGITAL ANOMALIES", "Pierre Robin sequence with facial and digital anomalies", "Pierre Robin sequence faciodigital anomaly syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pierre Robin syndrome-faciodigital anomaly syndrome", "shortest_name_length": 36}
{"curie": "UMLS:C2242600", "names": ["Catheter site irritation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Catheter site irritation", "shortest_name_length": 24}
{"curie": "UMLS:C0032024", "names": ["PITYRIASIS", "Pityriases", "Pityriasis", "pityriasis", "Pityriasis, NOS", "Pityriasis (disorder)", "pityriasis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pityriasis", "shortest_name_length": 10}
{"curie": "MONDO:0044811", "names": ["Schwalbe disease", "Ziehen-oppenheim disease", "primary torsion dystonia", "Idiopathic Torsion Dystonia", "idiopathic torsion dystonia", "Idiopathic torsion dystonia", "dystonia musculorum deformans", "dystonia deformans progressiva"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic torsion dystonia", "shortest_name_length": 16}
{"curie": "MONDO:0010049", "names": ["spastic paresis glaucoma mental retardation", "spastic paresis glaucoma intellectual disability", "Spastic Paresis, Glaucoma, and Mental Retardation", "SPASTIC PARESIS, GLAUCOMA, AND MENTAL RETARDATION", "spastic paresis, glaucoma, and mental retardation", "spastic paresis, glaucoma, and intellectual disability", "spastic paraplegia-glaucoma-intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic paraplegia-glaucoma-intellectual disability syndrome", "shortest_name_length": 43}
{"curie": "MONDO:0700134", "names": ["Bovine Neoplasm", "bovine neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bovine neoplasm", "shortest_name_length": 15}
{"curie": "UMLS:C5420157", "names": ["Ectopic PitNET/Adenoma", "Ectopic Pituitary Gland Adenoma", "Extrasellar Pituitary Gland Adenoma", "Ectopic Pituitary Neuroendocrine Tumor", "Ectopic Pituitary Neuroendocrine Tumor/Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ectopic Pituitary Neuroendocrine Tumor", "shortest_name_length": 22}
{"curie": "UMLS:C2828010", "names": ["Stage 0 Merkel Cell Carcinoma", "Stage 0 Merkel Cell Carcinoma AJCC v7", "stage 0 Merkel cell carcinoma in situ"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Merkel Cell Carcinoma AJCC v7", "shortest_name_length": 29}
{"curie": "UMLS:C5670682", "names": ["Stage IV Cervical Cancer FIGO 2009", "Stage IV Cervical Carcinoma FIGO 2009"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Cervical Cancer FIGO 2009", "shortest_name_length": 34}
{"curie": "UMLS:C1831740", "names": ["Long-Term Effects Secondary to Cancer Therapy in Adults", "long-term effects secondary to cancer therapy in adults"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Long-Term Effects Secondary to Cancer Therapy in Adults", "shortest_name_length": 55}
{"curie": "UMLS:C4525081", "names": ["Refractory Langerhans Cell Histiocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Langerhans Cell Histiocytosis", "shortest_name_length": 40}
{"curie": "UMLS:C1883513", "names": ["Utricle-Associated Mucosal Gland Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Utricle-Associated Mucosal Gland Hyperplasia", "shortest_name_length": 44}
{"curie": "UMLS:C0334399", "names": ["Luteinised thecoma", "Luteinized thecoma", "luteinized; thecoma", "thecoma; luteinized", "Thecoma, luteinized", "Thecoma, luteinised", "Luteinized Ovarian Thecoma", "Ovarian Luteinized Thecoma", "Luteinized Thecoma of Ovary", "Luteinized Thecoma of the Ovary", "Thecoma, luteinized (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thecoma, luteinized", "shortest_name_length": 18}
{"curie": "UMLS:C2939130", "names": ["Other bacterial diseases", "OTHER BACTERIAL DISEASES", "Other bacterial infections", "Other bacterial diseases (A30-A49)", "Other bacterial infections of unspecified site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Other bacterial diseases", "shortest_name_length": 24}
{"curie": "MONDO:0016776", "names": ["FFA", "frontal fibrosing alopecia", "Frontal fibrosing alopecia", "Frontal fibrosing alopecia (disorder)", "frontal fibrosing alopecia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontal fibrosing alopecia", "shortest_name_length": 3}
{"curie": "MONDO:0005789", "names": ["HDV", "Hepatitis D", "hepatitis d", "HEPATITIS D", "hepatitis D", "Delta Hepatitis", "HEPATITIS DELTA", "hepatitis delta", "Delta infection", "Delta Infection", "Hepatitis delta", "delta hepatitis", "Infection, Delta", "Hepatitis, Delta", "hepatitis type D", "hepatitis; Delta-", "Viral hepatitis D", "Delta-; hepatitis", "Infections, Delta", "Hepatitis D virus", "Hepatitides, Delta", "hepatitis D infection", "Hepatitis D Infection", "hepatitis, delta virus", "Viral hepatitis type D", "HEPATITIS, ACUTE DELTA", "hepatitis D virus infection", "Hepatitis D virus infection", "Hepatitis delta virus hepatitis", "Viral hepatitis type D (disorder)", "hepatitis, delta virus (diagnosis)", "Hepatitis delta virus caused hepatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatitis D virus infection", "shortest_name_length": 3}
{"curie": "MONDO:0007436", "names": ["DD-I", "DTDP1", "ROOTLESS TEETH", "Rootless teeth", "rootless teeth", "Missing tooth root", "Teeth without roots", "Aplasia of tooth root", "Absence of tooth root", "Agenesis of tooth root", "Dentin dysplasia type I", "dentin dysplasia type I", "DENTIN DYSPLASIA, TYPE I", "Dentin dysplasia, type 1", "dentin dysplasia, type 1", "Dentin dysplasia, type I", "dentin dysplasia, type I", "Dentin Dysplasia, Type I", "radicular dentin dysplasia", "RADICULAR DENTIN DYSPLASIA", "Radicular dentin dysplasia", "Radicular dentine dysplasia", "[OBSOLETE] Opalescent dentin", "DENTIN DYSPLASIA, SHIELDS TYPE I", "dentin dysplasia, Shields type 1", "Tooth with dentin dysplasia type i", "Dentine dysplasia - Shield's type I", "Dentin dysplasia, type I (disorder)", "dentin dysplasia, type i, with microdontia and misshapen teeth", "dentin dysplasia, type I, with extreme microdontia and misshapen teeth", "DENTIN DYSPLASIA, TYPE I, WITH EXTREME MICRODONTIA AND MISSHAPEN TEETH"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dentin dysplasia type I", "shortest_name_length": 4}
{"curie": "MONDO:0003478", "names": ["Ependymoma", "ependymoma", "Familial ependymoma", "Childhood ependymoma", "childhood ependymoma", "pediatric ependymoma", "Pediatric Ependymoma", "Childhood Ependymoma", "Ependymoma, Familial", "ependymoma, childhood", "childhood ependymomas", "ependymoma of childhood", "Adult intracranial ependymoma", "CNS tumor, childhood ependymoma", "CNS tumor, ependymoma, childhood", "brain tumor, childhood ependymoma", "brain tumor, ependymoma, childhood", "Brain tumor, child: Ependymoma/Ependymal tumors"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood ependymoma", "shortest_name_length": 10}
{"curie": "MONDO:0010648", "names": ["MDI", "MDX", "BPAD", "MAFD2", "manic-depressive illness", "Manic-Depressive Illness", "MANIC-DEPRESSIVE ILLNESS", "major affective disorder 2", "Major Affective Disorder 2", "MAJOR AFFECTIVE DISORDER 2", "BIPOLAR AFFECTIVE DISORDER", "bipolar affective disorder", "MAJOR affective disorder 2", "MANIC-DEPRESSIVE PSYCHOSIS, X-LINKED", "Manic-Depressive Psychosis, X-Linked", "manic-depressive psychosis, X-linked", "major affective disorder 2, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "major affective disorder 2", "shortest_name_length": 3}
{"curie": "MONDO:0007170", "names": ["ATRESIA OF EXTERNAL AUDITORY CANAL AND CONDUCTIVE DEAFNESS", "Atresia of External Auditory Canal and Conduction Deafness", "atresia of external auditory canal and conductive deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atresia of external auditory canal and conductive deafness", "shortest_name_length": 58}
{"curie": "UMLS:C4552688", "names": ["Stage IA Ovarian Cancer", "Stage IA Ovarian Cancer AJCC v8", "Stage IA Ovarian Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Ovarian Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "UMLS:C4553568", "names": ["Stage III Fallopian Tube Cancer", "Stage III Fallopian Tube Cancer AJCC v8", "Stage III Fallopian Tube Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Fallopian Tube Cancer AJCC v8", "shortest_name_length": 31}
{"curie": "MONDO:0003507", "names": ["Ovarian Choriocarcinoma", "ovarian choriocarcinoma", "choriocarcinoma of ovary", "Choriocarcinoma of ovary", "choriocarcinoma, ovarian", "Choriocarcinoma of Ovary", "Choriocarcinoma of the Ovary", "choriocarcinoma of the ovary", "ovary choriocarcinoma (disease)", "Ovarian Germ Cell Choriocarcinoma", "ovarian germ cell choriocarcinoma", "Ovarian germ cell choriocarcinoma", "germ cell choriocarcinoma of ovary", "Germ Cell Choriocarcinoma of Ovary", "Choriocarcinoma of ovary (disorder)", "choriocarcinoma of ovary (diagnosis)", "Germ Cell Choriocarcinoma of the Ovary", "germ cell choriocarcinoma of the ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choriocarcinoma of ovary", "shortest_name_length": 23}
{"curie": "UMLS:C4520748", "names": ["stage I hypopharynx cancer", "Stage I Hypopharyngeal Throat Cancer", "Stage I Hypopharynx Carcinoma AJCC v6", "Stage I Hypopharyngeal Carcinoma AJCC v6", "Stage I Carcinoma of Hypopharynx AJCC v6", "Stage I Carcinoma of the Hypopharynx AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Hypopharyngeal Carcinoma AJCC v6", "shortest_name_length": 26}
{"curie": "UMLS:C5238931", "names": ["Advanced Skin Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Skin Squamous Cell Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0020685", "names": ["infratentorial ependymal tumor", "Infratentorial Ependymal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infratentorial ependymal tumor", "shortest_name_length": 30}
{"curie": "MONDO:0004737", "names": ["Homocystinuria", "homocystinuria", "CBS deficiency", "HOMOCYSTINURIA", "Homocystinuria, NOS", "homocystinuria (disease)", "Homocystinuria (disorder)", "homocystinuria (diagnosis)", "High urine homocystine levels", "cystathionine synthase deficiency", "Cystathionine synthase deficiency", "cystathionine beta synthase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "homocystinuria", "shortest_name_length": 14}
{"curie": "UMLS:C4727587", "names": ["Methylated MGMT Glioblastoma", "MGMT-Methylated Glioblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MGMT-Methylated Glioblastoma", "shortest_name_length": 28}
{"curie": "MONDO:0015274", "names": ["Beryllioses", "BERYLLIOSIS", "Berylliosis", "berylliosis", "beryllioses", "Beryllliosis", "acute berylliosis", "beryllium disease", "Beryllium disease", "beryllium poisoning", "chronic berylliosis", "Beryllium poisoning", "Beryllium granuloma", "Chronic berylliosis", "beryllium; granuloma", "BERYLLIOSIS, CHRONIC", "granuloma; beryllium", "Subacute berylliosis", "Berylliosis, chronic", "poisoning by beryllium", "reversible berylliosis", "Berylliosis (disorder)", "Chronic beryllium lung", "chronic beryllium disease", "Chronic beryllium disease", "BERYLLIUM DISEASE, CHRONIC", "Chronic beryllium poisoning", "chronic pulmonary berylliosis", "Chronic berylliosis (disorder)", "chronic beryllium lung disease", "Chronic beryllium lung disease", "chronic berylliosis (diagnosis)", "lung; fibrosis, with berylliosis", "fibrosis; lung, with berylliosis", "poisoning by beryllium (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic beryllium disease", "shortest_name_length": 11}
{"curie": "UMLS:C5420544", "names": ["Recurrent Poorly Differentiated Thyroid Gland Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Poorly Differentiated Thyroid Gland Carcinoma", "shortest_name_length": 55}
{"curie": "UMLS:C4525095", "names": ["Stage IVA Colorectal Cancer AJCC v8", "Stage IVA Colorectal Carcinoma AJCC v8", "Stage IVA Colorectal (Colon or Rectal) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Colorectal Cancer AJCC v8", "shortest_name_length": 35}
{"curie": "MONDO:0008372", "names": ["retinal aplasia", "RETINAL APLASIA", "Retinal Aplasia", "Amaurosis Congenita", "amaurosis congenita", "AMAUROSIS CONGENITA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal aplasia", "shortest_name_length": 15}
{"curie": "UMLS:C0280177", "names": ["Stage IV Immunoblastic Lymphoma", "Stage IV Adult Immunoblastic Lymphoma", "stage IV adult immunoblastic lymphoma", "Ann Arbor Stage IV Adult Immunoblastic Lymphoma", "stage IV adult immunoblastic large cell lymphoma", "Stage IV Adult Immunoblastic Large Cell Lymphoma", "Adult Immunoblastic Large Cell Lymphoma Stage IV", "adult immunoblastic large cell lymphoma stage IV", "adult immunoblastic large cell lymphoma, stage IV", "metastatic adult immunoblastic large cell lymphoma", "adult immunoblastic large cell lymphoma, metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Adult Immunoblastic Lymphoma", "shortest_name_length": 31}
{"curie": "MONDO:0004832", "names": ["esophagus leiomyoma", "Esophagus Leiomyoma", "esophageal leiomyoma", "Esophageal Leiomyoma", "ESOPHAGUS, LEIOMYOMA", "Esophageal leiomyoma", "Oesophageal leiomyoma", "leiomyoma of esophagus", "Leiomyoma of Esophagus", "Leiomyoma of esophagus", "Leiomyoma of oesophagus", "leiomyoma of the esophagus", "Leiomyoma of the Esophagus", "Leiomyoma of esophagus (disorder)", "leiomyoma of esophagus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophagus leiomyoma", "shortest_name_length": 19}
{"curie": "MONDO:0009820", "names": ["OPS", "Ops", "OPPG", "osteoporosis pseudoglioma", "osteoporosis with pseudoglioma", "Osteoporosis with pseudoglioma", "pseudoglioma with bone fragility", "Pseudoglioma with bone fragility", "Osteoporosis Pseudoglioma Syndrome", "osteoporosis pseudoglioma syndrome", "OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME", "osteoporosis-pseudoglioma syndrome", "Osteoporosis-pseudoglioma syndrome", "osteogenesis imperfecta ocular form", "osteogenesis imperfecta, ocular form", "Osteogenesis imperfecta, ocular form", "OSTEOGENESIS IMPERFECTA, OCULAR FORM", "Ocular form of osteogenesis imperfecta", "ocular form of osteogenesis imperfecta", "osteoporosis-pseudoglioma syndrome (OPS)", "Osteoporosis with pseudoglioma (disorder)", "osteoporosis with pseudoglioma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteoporosis-pseudoglioma syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0003349", "names": ["CNS leiomyosarcoma", "CNS Leiomyosarcoma", "Leiomyosarcoma of CNS", "leiomyosarcoma of CNS", "Leiomyosarcoma of the CNS", "leiomyosarcoma of the CNS", "Central Nervous System Leiomyosarcoma", "central nervous system leiomyosarcoma", "leiomyosarcoma of central nervous system", "Leiomyosarcoma of Central Nervous System", "leiomyosarcoma of the central nervous system", "Leiomyosarcoma of the Central Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system leiomyosarcoma", "shortest_name_length": 18}
{"curie": "UMLS:C3897517", "names": ["Stage IVB Colon Cancer", "Stage IVB Colon Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Colon Cancer AJCC v7", "shortest_name_length": 22}
{"curie": "MONDO:0007168", "names": ["AO3", "AOIII", "Aoiii", "atelosteogenesis type 3", "Atelosteogenesis type 3", "Atelosteogenesis Type 3", "atelosteogenesis, type 3", "Atelosteogenesis type III", "atelosteogenesis type III", "Atelosteogenesis Type Iii", "atelosteogenesis, type III", "ATELOSTEOGENESIS, TYPE III", "Atelosteogenesis type 3 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atelosteogenesis type III", "shortest_name_length": 3}
{"curie": "UMLS:C5447322", "names": ["Immunodeficiencies Affecting Cellular and Humoral Immunity/ Combined Immune Deficiency", "Immunodeficiencies Affecting Cellular and Humoral Immunity - Combined Immune Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immunodeficiencies Affecting Cellular and Humoral Immunity - Combined Immune Deficiency", "shortest_name_length": 86}
{"curie": "MONDO:0018735", "names": ["MLT", "MLT1", "IMD12", "PCASP1", "DKFZp434L132", "MALT1 wt Allele", "MALT1 wt allele", "MALT1 Protease Gene", "Caspase-Like Protein Gene", "MALT1 Paracaspase wt Allele", "cutaneovisceral angiomatosis-thrombocytopenia syndrome", "multifocal lymphangioendotheliomatosis with thrombocytopenia", "Mucosa Associated Lymphoid Tissue Lymphoma Translocation Gene 1", "multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome", "mucosa associated lymphoid tissue lymphoma translocation Gene 1 wt allele"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C4552683", "names": ["Stage I Urethral Cancer", "Stage I Urethral Cancer AJCC v8", "Stage I Urethral Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Urethral Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "MONDO:0008076", "names": ["HNA", "NAPB", "Neuralgic amyotrophy", "neuralgic amyotrophy", "Neuralgic Amyotrophy", "Amyotrophic Neuralgia", "amyotrophy; neuralgic", "Amyotrophy, Neuralgic", "amyotrophic neuralgia", "neuralgic; amyotrophy", "Neuralgic Amyotrophies", "Amyotrophic Neuralgias", "Neuralgia, Amyotrophic", "Neuralgias, Amyotrophic", "Amyotrophies, Neuralgic", "Brachial plexus neuritis", "Neuralgic shoulder amyotrophy", "Acute brachial plexus neuritis", "Neuralgic amyotrophy (disorder)", "hereditary neuralgic amyotrophy", "Hereditary Neuralgic Amyotrophy", "Neuralgic Amyotrophy, Hereditary", "neuralgic amyotrophy (diagnosis)", "Amyotrophy, Hereditary Neuralgic", "AMYOTROPHY, HEREDITARY NEURALGIC", "amyotrophy, hereditary neuralgic", "Immune brachial plexus neuropathy", "Hereditary Neuralgic Amyotrophies", "Familial Brachial Plexus Neuritis", "Amyotrophies, Hereditary Neuralgic", "Neuralgic Amyotrophies, Hereditary", "NEURITIS WITH BRACHIAL PREDILECTION", "neuritis with brachial predilection", "Neuritis With Brachial Predilection", "hereditary brachial plexus neuropathy", "Hereditary Brachial Plexus Neuropathy", "BRACHIAL PLEXUS NEUROPATHY, HEREDITARY", "brachial plexus neuropathy, hereditary", "Brachial Plexus Neuropathy, Hereditary", "Mononeuritis multiplex with brachial predilection", "Heredofamilial Neuritis with Brachial Plexus Predilection", "Amyotrophy, Hereditary Neuralgic, with Predilection for Brachial Plexus", "AMYOTROPHY, HEREDITARY NEURALGIC, WITH PREDILECTION FOR BRACHIAL PLEXUS", "amyotrophy, hereditary neuralgic, with predilection for brachial plexus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyotrophic neuralgia", "shortest_name_length": 3}
{"curie": "MONDO:0008293", "names": ["Dsap", "DSAP1", "POROK3", "porokeratosis 3, multiple types", "POROKERATOSIS 3, MULTIPLE TYPES", "Porokeratosis, disseminated superficial actinic 1", "porokeratosis, disseminated superficial actinic 1", "Porokeratosis, Disseminated Superficial Actinic, 1", "porokeratosis, disseminated superficial actinic, 1", "POROKERATOSIS, DISSEMINATED SUPERFICIAL ACTINIC, 1", "POROKERATOSIS 3, DISSEMINATED SUPERFICIAL ACTINIC TYPE", "porokeratosis 3, disseminated superficial actinic type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "porokeratosis 3, disseminated superficial actinic type", "shortest_name_length": 4}
{"curie": "UMLS:C4053762", "names": ["Congenital Renal Hypoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Renal Hypoplasia", "shortest_name_length": 27}
{"curie": "UMLS:C4520756", "names": ["Stage I Larynx Verrucous Carcinoma", "Stage I Verrucous Carcinoma of Larynx", "Stage I Laryngeal Verrucous Carcinoma", "Stage I Verrucous Carcinoma of the Larynx", "Stage I Laryngeal Throat Verrucous Cancer", "Stage I Laryngeal Verrucous Carcinoma AJCC v6", "Stage I Laryngeal Verrucous Carcinoma AJCC v7", "Stage I Laryngeal Verrucous Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Laryngeal Verrucous Carcinoma AJCC v6 and v7", "shortest_name_length": 34}
{"curie": "UMLS:C1739418", "names": ["Acute cardiac toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute cardiac toxicity", "shortest_name_length": 22}
{"curie": "MONDO:0021154", "names": ["dermis disease", "dermis disorder", "disease of dermis", "disorder of dermis", "other dermis disorder", "dermis disease or disorder", "disease or disorder of dermis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermis disorder", "shortest_name_length": 14}
{"curie": "MONDO:0025397", "names": ["Distemper", "distemper", "Distempers", "distempered", "canine distemper", "distemper, canine", "canine Distempers", "Distempers, canine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canine distemper", "shortest_name_length": 9}
{"curie": "MONDO:0008376", "names": ["Venous beading", "Retinal veins beaded", "RETINAL VENOUS BEADING", "retinal venous beading", "Retinal venous beading", "Retinal veins beaded (finding)", "retinal venous beading (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal venous beading", "shortest_name_length": 14}
{"curie": "MONDO:0001471", "names": ["HISTOPLASMA MENINGITIS", "Meningitis histoplasma", "Histoplasmosis meningitis", "histoplasmosis meningitis", "Histoplasmosis with meningitis", "histoplasmosis with meningitis", "Histoplasmosis, unspecified, meningitis", "histoplasmosis with meningitis (diagnosis)", "Histoplasma capsulatum infectious meningitis", "Histoplasma capsulatum caused infectious meningitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "histoplasmosis meningitis", "shortest_name_length": 22}
{"curie": "MONDO:0012168", "names": ["DYX8", "dyslexia, susceptibility to, 8", "DYSLEXIA, SUSCEPTIBILITY TO, 8", "dyslexia, susceptibility to, 8, multifactorial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyslexia, susceptibility to, 8", "shortest_name_length": 4}
{"curie": "UMLS:C1512694", "names": ["CELLULARITY, INCREASED", "Increased Cellularity Present"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Increased Cellularity Present", "shortest_name_length": 22}
{"curie": "MONDO:0012628", "names": ["CHDS8", "coronary heart disease, susceptibility to, 8", "CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coronary heart disease, susceptibility to, 8", "shortest_name_length": 5}
{"curie": "UMLS:C0266717", "names": ["acardius", "Acardius", "Acardiacus", "acardiac twin", "TRAP Sequence", "Acardiac Twin", "Acardiac twins", "acardiac twins", "Acardiac twins, NOS", "Acardius (disorder)", "Acardiac monster, NOS", "Acardiac Malformation", "TRAP sequence malformation", "Twin reversed arterial perfusion sequence malformation", "Twin Reversed Arterial Perfusion Sequence Malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acardius", "shortest_name_length": 8}
{"curie": "MONDO:0010569", "names": ["X-linked partial corpus callosum agenesis", "X-linked partial agenesis of corpus callosum", "X-linked complicated corpus callosum agenesis", "Corpus Callosum, Partial Agenesis of, X-Linked", "corpus callosum, partial agenesis of, X-linked", "CORPUS CALLOSUM, PARTIAL AGENESIS OF, X-LINKED", "x-linked complicated corpus callosum dysgenesis", "X-linked complicated corpus callosum dysgenesis", "corpus callosum, partial agenesis of, X-linked recessive", "X-linked complicated corpus callosum dysgenesis (disorder)", "x-linked complicated corpus callosum dysgenesis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked complicated corpus callosum dysgenesis", "shortest_name_length": 41}
{"curie": "UMLS:C1328588", "names": ["Rectal Mucositis", "Rectal mucositis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rectal Mucositis", "shortest_name_length": 16}
{"curie": "MONDO:0024879", "names": ["METASTATIC CARCINOMA", "Metastatic carcinoma", "carcinoma metastatic", "metastatic carcinoma", "Metastatic Carcinoma", "Carcinoma, metastatic", "Carcinoma, metastatic NOS", "Carcinoma, metastatic, NOS", "Carcinoma, metastatic (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metastatic carcinoma", "shortest_name_length": 20}
{"curie": "UMLS:C0854832", "names": ["Angiocentric Lymphoma Refractory", "Refractory Angiocentric Lymphoma", "Nasal T-cell lymphoma refractory", "Angiocentric lymphoma refractory", "Polymorphic reticulosis refractory", "Refractory Nasal/Nasal Type T/NK-Cell Lymphoma", "Refractory Nasal Type Extranodal NK/T-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Angiocentric lymphoma refractory", "shortest_name_length": 32}
{"curie": "MONDO:0018166", "names": ["OSMF", "Oral Submucous Fibroses", "oral submucous fibrosis", "Oral Submucous Fibrosis", "Oral submucous fibrosis", "Fibrosis, Oral Submucous", "Submucous Fibroses, Oral", "Oral submucosal fibrosis", "Fibroses, Oral Submucous", "oral submucosal fibrosis", "Submucous Fibrosis, Oral", "oral cavity submucous fibrosis", "Oral Cavity Submucous Fibrosis", "Oral cavity Submucous Fibrosis", "Oral submucosal fibrosis (disorder)", "Oral submucous fibrosis, incl of tongue", "oral submucosal fibrosis including tongue", "Oral submucous fibrosis, including of tongue", "Oral submucosal fibrosis, including of tongue", "oral submucosal fibrosis, including of tongue", "oral submucosal fibrosis including tongue (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oral submucous fibrosis", "shortest_name_length": 4}
{"curie": "MONDO:0021208", "names": ["Endocrine alopecia", "endocrine alopecia", "Alopecia, endocrine", "Endocrine alopecia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endocrine alopecia", "shortest_name_length": 18}
{"curie": "MONDO:0014917", "names": ["DEE42", "EIEE42", "early infantile epileptic encephalopathy 42", "epileptic encephalopathy, early infantile, 42", "Developmental and Epileptic Encephalopathy 42", "Epileptic Encephalopathy, Early Infantile, 42", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 42", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 42", "developmental and epileptic encephalopathy 42", "developmental and epileptic encephalopathy, 42", "CACNA1A early infantile epileptic encephalopathy", "epileptic encephalopathy, early infantile, type 42", "epileptic encephalopathy, early infantile, 42; EIEE42", "early infantile epileptic encephalopathy caused by mutation in CACNA1A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 42", "shortest_name_length": 5}
{"curie": "MONDO:0040699", "names": ["Necrotizing Scleritis", "scleritis necrotizing", "necrotizing scleritis", "Necrotising scleritis", "Necrotizing scleritis", "Scleritis, Necrotizing", "Necrotizing Scleritides", "Scleritides, Necrotizing", "Necrotizing scleritis (disorder)", "Necrotizing scleritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "necrotizing scleritis", "shortest_name_length": 21}
{"curie": "MONDO:0018058", "names": ["trachea; absent", "tracheal absence", "absence; trachea", "Tracheal Absence", "tracheal agenesis", "Tracheal agenesis", "Tracheal Agenesis", "agenesis; trachea", "trachea; agenesis", "agenesis of trachea", "Agenesis of trachea", "congenital tracheal agenesis", "Congenital tracheal agenesis", "Congenital Absence of Trachea", "congenital absence of trachea", "Congenital absence of trachea", "Agenesis of trachea (disorder)", "Absence or agenesis of trachea", "agenesis of trachea (diagnosis)", "Congenital absence of trachea (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tracheal agenesis", "shortest_name_length": 15}
{"curie": "MONDO:0700024", "names": ["chromosome 19 disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 19 disorder", "shortest_name_length": 22}
{"curie": "UMLS:C1370962", "names": ["stage C prostate cancer", "Prostate cancer stage C", "Stage C Prostate Cancer", "prostate cancer, stage C", "Stage C Prostate Carcinoma", "stage C cancer of the prostate", "cancer of the prostate, stage C", "stage C carcinoma of the prostate", "carcinoma of the prostate, stage C"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate cancer stage C", "shortest_name_length": 23}
{"curie": "UMLS:C0278870", "names": ["Recurrent Uveal Melanoma", "recurrent uveal melanoma", "melanoma, uveal recurrent", "uveal melanoma, recurrent", "Recurrent Melanoma of Uvea", "recurrent intraocular melanoma", "Recurrent Melanoma of the Uvea", "intraocular melanoma, recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Uveal Melanoma", "shortest_name_length": 24}
{"curie": "UMLS:C3665444", "names": ["Nnutrophilia", "Neutrophilia", "NEUTROPHILIA", "neutrophilia", "Neutrocytosis", "Neutrophilia, NOS", "Neutrophilia disorder", "Neutrophilia (disorder)", "neutrophilia (diagnosis)", "Neutrophilic leukocytosis", "neutrophilic leucocytosis", "neutrophilic leukocytosis", "Neutrophilia disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neutrophilia (disorder)", "shortest_name_length": 12}
{"curie": "UMLS:C3642460", "names": ["Perinatal Drug Withdrawal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perinatal Drug Withdrawal", "shortest_name_length": 25}
{"curie": "MONDO:0016359", "names": ["Scleroderma, sine", "limited systemic sclerosis", "SSC without Skin Involvement", "SSC without skin involvement", "Systemic Sclerosis sine Scleroderma", "Systemic sclerosis sine scleroderma", "systemic sclerosis sine scleroderma", "Systemic sclerosis without skin thickening", "Systemic Sclerosis without Skin Involvement", "systemic sclerosis without skin involvement", "Systemic sclerosis sine scleroderma (disorder)", "progressive systemic sclerosis sine scleroderma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "limited systemic sclerosis", "shortest_name_length": 17}
{"curie": "MONDO:0010142", "names": ["RTSH", "CHNG1", "TSH RESISTANCE", "TSH resistance", "THYROTROPIN RESISTANCE", "thyrotropin resistance", "hypothyroidism, Nonautoimmune", "Hypothyroidism, Nonautoimmune", "HYPOTHYROIDISM, NONAUTOIMMUNE", "congenital nongoitrous hypothryoidism 1", "congenital nongoitrous hypothyroidism 1", "hypothyroidism, congenital, nongoitrous, 1", "thyroid-stimulating hormone, resistance to", "THYROID-STIMULATING HORMONE, RESISTANCE TO", "Thyroid-Stimulating Hormone, Resistance To", "Hypothyroidism, Congenital, Nongoitrous, 1", "HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1", "Hypothyroidism due to TSH receptor mutation", "hypothyroidism due to TSH receptor mutations", "Hypothyroidism due to TSH receptor mutations", "hypothyroidism, congenital, nongoitrous, type 1", "hypothyroidism, congenital, due to TSH resistance", "HYPOTHYROIDISM, CONGENITAL, DUE TO TSH RESISTANCE", "Hypothyroidism, Congenital, Due To Tsh Resistance", "hypothyroidism due to unresponsiveness to thyrotropin", "HYPOTHYROIDISM DUE TO UNRESPONSIVENESS TO THYROTROPIN", "Hypothyroidism Due To Unresponsiveness To Thyrotropin", "Hypothyroidism due to TSHR (thyroid stimulating hormone receptor) mutation", "Congenital hypothyroidism due to thyroid stimulating hormone receptor mutation", "Congenital hypothyroidism due to thyroid stimulating hormone receptor mutation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypothyroidism due to TSH receptor mutations", "shortest_name_length": 4}
{"curie": "MONDO:0700081", "names": ["RDS", "NRDS", "newborn rds", "Infant ARDS", "RDS, type I", "infant ARDS", "newborns rds", "RDS - infants", "RDS of newborn", "IRDS of newborn", "RDS Of newborns", "RDS of prematurity", "Hyaline Membrane Disease", "Hyaline membrane disease", "HYALINE MEMBRANE DISEASE", "hyaline membrane disease", "Disease, Hyaline Membrane", "Hyaline Membrane Diseases", "Diseases, Hyaline Membrane", "Wet lung disease of newborn", "respiratory distress newborn", "newborn respiratory distress", "distress newborn respiratory", "distress newborns respiratory", "Neonatal Respiratory Distress", "respiratory syndrome distress", "Respiratory Distress Syndrome", "neonatal respiratory distress", "respiratory distress syndrome", "Congenital alveolar dysplasia", "distress respiratory syndrome", "distress; respiratory, newborn", "HMD - hyaline membrane disease", "HMD - Hyaline membrane disease", "distress respiratory syndromes", "RESP DISTRESS SYNDROME NEONATAL", "respiratory distress of newborn", "Respiratory distress of newborn", "Pulmonary hyaline membrane disease", "pulmonary hyaline membrane disease", "infant respiratory distress syndrome", "Infant respiratory distress syndrome", "Newborn Respiratory Distress Syndrome", "newborn respiratory distress syndrome", "SYNDROME RESPIRATORY DISTRESS NEWBORN", "Syndrome respiratory distress newborn", "RESPIRATORY DISTRESS SYNDROME NEWBORN", "Respiratory Distress Syndrome, Infant", "Distress respiratory syndrome newborn", "Respiratory distress syndrome newborn", "DISTRESS RESPIRATORY SYNDROME NEWBORN", "respiratory distress syndrome, infant", "Neonatal Respiratory Distress Syndrome", "neonatal respiratory distress syndrome", "Neonatal respiratory Distress syndrome", "Neonatal respiratory distress syndrome", "Respiratory Distress Syndrome, Newborn", "Infantile Respiratory Distress Syndrome", "Surfactant deficiency syndrome neonatal", "SURFACTANT DEFICIENCY SYNDROME NEONATAL", "RESPIRATORY DISTRESS SYNDROME, NEONATAL", "Respiratory distress syndrome in newborn", "Respiratory distress syndrome of newborn", "respiratory distress newborn (diagnosis)", "Respiratory distress syndrome in neonate", "RESPIRATORY DISTRESS SYNDROME, PERINATAL", "Idiopathic respiratory distress syndrome", "Respiratory distress syndrome (neonatal)", "respiratory distress syndrome of newborn", "Respiratory Distress Syndrome of Newborns", "respiratory distress syndrome Of newborns", "RESPIRATORY DISTRESS SYNDROME, IDIOPATHIC", "idiopathic respiratory distress of newborn", "Infant acute respiratory distress syndrome", "infant acute respiratory distress syndrome", "pulmonary hypoperfusion syndrome of newborn", "Pulmonary hypoperfusion syndrome of newborn", "Respiratory distress syndrome in the newborn", "Respiratory distress of newborn, unspecified", "Respiratory Distress Syndrome in the Newborn", "respiratory distress syndrome in the newborn", "Idiopathic respiratory distress syndrome, NOS", "Cardiorespiratory distress syndrome of newborn", "RDS, respiratory distress syndrome Of newborns", "RDS - Respiratory distress syndrome of newborn", "respiratory distress syndrome Of newborns (RDS)", "IRDS - Idiopathic respiratory distress syndrome", "syndrome Of newborns (RDS), respiratory distress", "newborns (RDS), respiratory distress syndrome Of", "respiratory distress syndrome in premature infants", "Idiopathic respiratory distress syndrome of newborn", "respiratory distress syndrome of newborn (diagnosis)", "respiratory; distress, syndrome (idiopathic) (newborn)", "distress; respiratory, syndrome (idiopathic) (newborn)", "Respiratory distress syndrome in the newborn (disorder)", "Idiopathic respiratory distress syndrome [IRDS or RDS] of newborn"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "newborn respiratory distress syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0002120", "names": ["NEC", "neuroendocrine cancer", "Neuroendocrine Cancer", "Neuroendocrine Carcinoma", "carcinoma neuroendocrine", "neuroendocrine carcinoma", "Neuroendocrine carcinoma", "carcinoma, neuroendocrine", "Neuroendocrine Carcinomas", "neuroendocrine carcinomas", "Carcinoma, Neuroendocrine", "Carcinomas, Neuroendocrine", "Neuroendocrine cancer, NOS", "Neuroendocrine carcinoma, NOS", "Neuroendocrine carcinoma (disorder)", "neuroendocrine carcinoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuroendocrine carcinoma", "shortest_name_length": 3}
{"curie": "MONDO:0010104", "names": ["Stoelinga de Koomen Davis syndrome", "Stoelinga-de Koomen-Davis syndrome", "Non erupted teeth with maxillary hypoplasia and genu valgum", "non erupted teeth with maxillary hypoplasia and genu valgum", "Teeth noneruption of with maxillary hypoplasia and genu valgum", "teeth noneruption of with maxillary hypoplasia and genu valgum", "non-eruption of teeth-maxillary hypoplasia-genu valgum syndrome", "Non-eruption of teeth-maxillary hypoplasia-genu valgum syndrome", "teeth, noneruption of, with maxillary hypoplasia and genu valgum", "Teeth, Noneruption of, With Maxillary Hypoplasia and Genu Valgum", "TEETH, NONERUPTION OF, WITH MAXILLARY HYPOPLASIA AND GENU VALGUM", "Non-eruption of teeth, maxillary hypoplasia, genu valgum syndrome", "Non-eruption of teeth, maxillary hypoplasia, genu valgum syndrome (disorder)", "Multiple non-erupting teeth, maxillo-zygomatical hypoplasia and other congenital defects", "multiple non-erupting teeth, maxillo-zygomatical hypoplasia and other congenital defects", "multiple none-erupting teeth, maxillo-zygomatical hypoplasia and other congenital defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-eruption of teeth-maxillary hypoplasia-genu valgum syndrome", "shortest_name_length": 34}
{"curie": "UMLS:C0751747", "names": ["Type III Nonketotic Hyperglycinemia", "Non-ketotic hyperglycinemia type III", "Nonketotic Hyperglycinemia, Type III", "Hyperglycinemia, Nonketotic, Type III", "Non-ketotic hyperglycinaemia type III", "Non-ketotic hyperglycinemia H protein deficiency", "Non-ketotic hyperglycinaemia H protein deficiency", "Non-ketotic hyperglycinemia H protein deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyperglycinemia, Nonketotic, Type III", "shortest_name_length": 35}
{"curie": "MONDO:0016184", "names": ["qualitative or quantitative defects of protein O-mannosyltransferase 1", "qualitative or quantitative defects of protein O-mannosyltransferase type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of protein O-mannosyltransferase 1", "shortest_name_length": 70}
{"curie": "MONDO:0008256", "names": ["PMF", "platelet membrane fluidity", "PLATELET MEMBRANE FLUIDITY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "platelet membrane fluidity", "shortest_name_length": 3}
{"curie": "UMLS:C2081572", "names": ["insertion; low", "low; insertion", "Low lying placenta", "Low-Lying Placenta", "low-lying placenta", "PLACENTA LOW LYING", "placenta low lying", "low lying placenta", "placenta; low lying", "low; lying placenta", "low-lying; placenta", "Low lying placenta (finding)", "low-lying placenta (diagnosis)", "a low-lying placenta was observed", "low-lying placenta (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low lying placenta", "shortest_name_length": 14}
{"curie": "UMLS:C0855056", "names": ["Leiomyosarcoma Metastatic", "Metastatic leiomyosarcoma", "Metastatic Leiomyosarcoma", "Leiomyosarcoma metastatic", "Metastatic leiomyosarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic leiomyosarcoma", "shortest_name_length": 25}
{"curie": "MONDO:0023054", "names": ["Klumpke", "Klumpke Palsy", "Klumpkes Palsy", "Klumpke's palsy", "Klumpke's Palsy", "klumpke's palsy", "Palsy, Klumpke's", "Klumpke paralysis", "klumpke paralysis", "Klumpke Paralysis", "klumpkes paralysis", "Klumpke; paralysis", "Paralysis, Klumpke", "paralysis; Klumpke", "klumpke's paralysis", "Klumpke's paralysis", "Dejerine-Klumpke palsy", "Dejerine Klumpke Palsy", "Dejerine-Klumpke Palsy", "Palsy, Dejerine-Klumpke", "Klumpke-Dejerine paralysis", "Klumpke Dejerine paralysis", "Klumpke-Déjerine paralysis", "klumpke-dejerine paralysis", "klumpke-dC)jerine paralysis", "Lower Brachial Plexus Palsy", "Lower brachial plexus palsy", "Klumpke-DC)jerine paralysis", "Lower brachial paralysis syndrome", "Dejerine-Klumpke palsy (diagnosis)", "Klumpke-Déjerine paralysis (disorder)", "Paralysis of the Lower Brachial Plexus", "Klumpke Dejerine brachial plexus injury", "Klumpke-Déjerine brachial plexus injury", "klumpke-dC)jerine brachial plexus injury", "Klumpke-DC)jerine brachial plexus injury", "lower brachial plexus palsy (Dejerine-Klumpke)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "klumpke's paralysis", "shortest_name_length": 7}
{"curie": "UMLS:C4721698", "names": ["Metastatic Renal Cell Cancer", "renal cell carcinoma metastatic", "metastatic renal cell carcinoma", "Metastatic Renal Cell Carcinoma", "RENAL CELL CARCINOMA METASTATIC", "Metastatic renal cell carcinoma", "Metastatic renal cell carcinoma (disorder)", "Metastatic renal cell carcinoma (diagnosis)", "renal malignant carcinoma renal cell metastatic", "Metastatic renal cell carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Renal Cell Carcinoma", "shortest_name_length": 28}
{"curie": "UMLS:C2981710", "names": ["IIIC", "Stage IIIC Uveal Melanoma", "Stage IIIC Uveal Melanoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Uveal Melanoma AJCC v7", "shortest_name_length": 4}
{"curie": "UMLS:C5555179", "names": ["Refractory Ovarian High-Grade Serous Adenocarcinoma", "Refractory Ovarian High Grade Serous Adenocarcinoma", "Refractory High Grade Ovarian Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Ovarian High Grade Serous Adenocarcinoma", "shortest_name_length": 51}
{"curie": "UMLS:C5418769", "names": ["Recurrent Platinum-Resistant Primary Peritoneal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Platinum-Resistant Primary Peritoneal Carcinoma", "shortest_name_length": 57}
{"curie": "UMLS:C5420755", "names": ["Conjunctival Spindle Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conjunctival Spindle Cell Carcinoma", "shortest_name_length": 35}
{"curie": "MONDO:0002705", "names": ["Breast Mucinous Cystadenocarcinoma", "breast mucinous cystadenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast mucinous cystadenocarcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0006891", "names": ["SEIZURE FOCAL MOTOR", "focal motor seizure", "Focal Motor Seizure", "Focal motor seizure", "motor focal epilepsy", "focal motor seizures", "FOCAL MOTOR EPILEPSY", "Focal Motor Epilepsy", "Focal motor seizures", "Focal seizure, motor", "epilepsy, focal motor", "Partial motor seizure", "motor partial seizure", "Motor Epilepsy, Focal", "Epilepsy, Focal Motor", "Partial Motor Seizure", "Partial motor attacks", "Partial seizure, motor", "Motor Seizure Disorder", "Partial motor seizures", "partial motor epilepsy", "Localized motor seizure", "Seizure Disorder, Motor", "Segmental motor seizure", "Epilepsy, Motor Partial", "Motor Seizure Disorders", "Epilepsy, motor partial", "Localised motor seizure", "epilepsy; motor partial", "Partial Epilepsy, Motor", "Focal motor seizure, NOS", "Epilepsy, Partial, Motor", "Seizure Disorders, Motor", "Localised motor seizures", "Localized motor seizures", "Epilepsy, focal motor NOS", "Motor Partial Seizure Disorder", "Focal motor seizure (disorder)", "Partial Seizure Disorder, Motor", "Seizure Disorder, Partial, Motor", "motor partial seizure (diagnosis)", "Simple partial seizures with motor signs", "Simple partial seizure with motor dysfunction", "Simple partial seizure with motor dysfunction (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial motor epilepsy", "shortest_name_length": 19}
{"curie": "MONDO:0019471", "names": ["ATLL", "atll", "t-all", "adult t cell leukemia", "Adult T-cell leukemia", "adult T cell leukemia", "t cell acute leukemia", "Adult T-Cell Leukemia", "adult T-cell lymphoma", "Adult T-cell lymphoma", "human t cell leukemia", "leukemia adult T-cell", "adult t-cell leukemia", "adult t-cell lymphoma", "adult T-cell leukemia", "human T cell leukemia", "adult T-cell; lymphoma", "adult t-cell leukemias", "adult T-cell; leukemia", "Leukemia, Adult T Cell", "adult T-cell leukaemia", "Adult T-Cell Leukemias", "leukemia; adult T-cell", "Leukemia, Adult T-Cell", "Adult T-cell leukaemia", "T Cell Leukemia, Adult", "T-Cell Leukemia, Adult", "lymphoma; adult T-cell", "lymphoma; T-cell, adult", "T-cell; lymphoma, adult", "T-Cell Leukemias, Adult", "Leukemias, Adult T-Cell", "T-cell leukemia of adults", "adult T-cell leukemia/lymphoma", "Adult T-cell leukemia/lymphoma", "adult T cell lymphoma/leukemia", "Adult T-Cell Leukemia-Lymphoma", "Adult T-Cell Leukemia/Lymphoma", "Adult T-cell leukemia-lymphoma", "Adult T Cell Lymphoma/Leukemia", "Adult T-cell lymphoma/leukemia", "Human T-Cell Leukemia-Lymphoma", "Human T Cell Leukemia Lymphoma", "Adult T-Cell Lymphoma/Leukemia", "adult T-cell lymphoma/leukemia", "Leukemia Lymphoma, Adult T Cell", "Adult T-cell leukaemia/lymphoma", "Leukemia-Lymphoma, Human T-Cell", "T-cell leukemia/lymphoma, adult", "T-Cell Leukemia-Lymphoma, Adult", "T Cell Leukemia Lymphoma, Adult", "T-Cell Leukemia-Lymphoma, Human", "leukemia/lymphoma, adult T-cell", "Human T-Cell Leukemia-Lymphomas", "Leukemia-Lymphoma, Adult T-Cell", "Adult T-cell lymphoma/leukaemia", "Adult T-Cell Leukemia-Lymphomas", "T-Cell Leukemia-Lymphomas, Adult", "Leukemia-Lymphomas, Human T-Cell", "T-Cell Leukemia-Lymphomas, Human", "Leukemia-Lymphomas, Adult T-Cell", "Adult T-cell lymphomas/leukemias", "Adult T-cell lymphomas/leukaemias", "HTLV Associated Leukemia Lymphoma", "adult T-cell leukemia (diagnosis)", "HTLV-Associated Leukemia-Lymphoma", "Leukemia-Lymphoma, HTLV-Associated", "Adult T-cell lymphoma/leukemia NOS", "HTLV-Associated Leukemia-Lymphomas", "Leukemia-Lymphomas, HTLV-Associated", "Adult T-cell lymphoma/leukaemia NOS", "Adult T-cell leukemia/lymphoma (clinical)", "Adult T-cell leukemia/lymphoma (disorder)", "Adult T-cell lymphoma/leukemia (HTLV-1 +)", "HTLV I Associated T Cell Leukemia Lymphoma", "Adult T-cell leukemia/lymphoma (diagnosis)", "Adult T-cell lymphoma/leukaemia (HTLV-1 +)", "Adult T-cell leukaemia/lymphoma (clinical)", "HTLV-I-Associated T-Cell Leukemia-Lymphoma", "T Cell Leukemia Lymphoma, HTLV I Associated", "HTLV-I-Associated T-Cell Leukemia-Lymphomas", "Leukemia-Lymphoma, HTLV-I-Associated T-Cell", "T-Cell Leukemia-Lymphoma, HTLV-I-Associated", "Leukemia-Lymphomas, HTLV-I-Associated T-Cell", "T-Cell Leukemia-Lymphomas, HTLV-I-Associated", "HTLV-1 associated adult T-cell lymphoma/leukemia", "HTLV-I associated adult T-cell leukemia/lymphoma", "HTLV-1 Associated Adult T-Cell Lymphoma/Leukemia", "HTLV-I Associated Adult T-Cell Leukemia/Lymphoma", "Adult T-cell leukemia/lymphoma (HTLV-1 positive)", "adult T-cell leukaemia/lymphoma (HTLV-1 positive)", "Adult T-cell leukaemia/lymphoma (HTLV-1 positive)", "Adult T-cell lymphoma/leukemia (HTLV-1-associated)", "Leukemia-Lymphoma, T-Cell, Acute, HTLV-I-Associated", "Leukemia Lymphoma, T Cell, Acute, HTLV I Associated", "Adult T-cell lymphoma/leukemia (HTLV-1-associated) NOS", "Human T Lymphotropic Virus Associated Leukemia Lymphoma", "Human T Lymphotropic Virus-Associated Leukemia-Lymphoma", "Adult T-cell leukemia/lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult T-cell leukemia/lymphoma", "shortest_name_length": 4}
{"curie": "MONDO:0006417", "names": ["small intestine diffuse large B-cell lymphoma", "Small Intestinal Diffuse Large B-Cell Lymphoma", "small intestinal diffuse large B-cell lymphoma", "diffuse large B-cell lymphoma of small intestine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small intestinal diffuse large B-cell lymphoma", "shortest_name_length": 45}
{"curie": "UMLS:C1096358", "names": ["Intervertebral disc compression"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intervertebral disc compression", "shortest_name_length": 31}
{"curie": "UMLS:C1167745", "names": ["Extremity necrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extremity necrosis", "shortest_name_length": 18}
{"curie": "UMLS:C4683628", "names": ["St. Jude Childhood Non-Hodgkin Lymphoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "St. Jude Childhood Non-Hodgkin Lymphoma by AJCC v8 Stage", "shortest_name_length": 56}
{"curie": "UMLS:C0311298", "names": ["Propionic acidemia, type II", "Propionic acidaemia, type II", "Propionyl-CoA carboxylase deficiency", "Propionic acidemia, type II (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Propionic acidemia, type II", "shortest_name_length": 27}
{"curie": "UMLS:C0280391", "names": ["hypopharynx squamous cell carcinoma, stage IV", "Hypopharyngeal squamous cell carcinoma stage IV", "hypopharynx squamous cell carcinoma, metastatic", "hypopharyngeal squamous cell carcinoma, stage IV", "epidermoid carcinoma of the hypopharynx, stage IV", "Metastatic Hypopharyngeal Squamous Cell Carcinoma", "hypopharyngeal squamous cell carcinoma, metastatic", "epidermoid carcinoma of the hypopharynx, metastatic", "stage IV squamous cell carcinoma of the hypopharynx", "Squamous cell carcinoma of the hypopharynx stage IV", "squamous cell carcinoma of the hypopharynx, stage IV", "Metastatic Hypopharyngeal Throat Squamous Cell Cancer", "Metastatic Squamous Cell Carcinoma of the Hypopharynx", "metastatic squamous cell carcinoma of the hypopharynx", "squamous cell carcinoma of the hypopharynx, metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Squamous cell carcinoma of the hypopharynx stage IV", "shortest_name_length": 45}
{"curie": "UMLS:C1334004", "names": ["High Grade Gastric Intraepithelial Neoplasia", "High-Grade Gastric Glandular Intraepithelial Neoplasia", "High-Grade Gastric Intraepithelial Neoplasia (Dysplasia)", "High-Grade Gastric Glandular Intraepithelial Neoplasia (Dysplasia)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Gastric Intraepithelial Neoplasia", "shortest_name_length": 44}
{"curie": "MONDO:0004965", "names": ["ACCC", "Acinar carcinoma", "acinar carcinoma", "Acinar Carcinoma", "acinic cell tumor", "Acinic Cell Tumor", "Acinar Carcinomas", "Carcinoma, Acinar", "Acinic Cell Tumors", "Carcinomas, Acinar", "Tumor, Acinic Cell", "Tumors, Acinic Cell", "Acinar adenocarcinoma", "Acinic cell carcinoma", "acinar adenocarcinoma", "Acinar Cell Carcinoma", "Acinar Adenocarcinoma", "acinic cell carcinoma", "acinar cell carcinoma", "Acinic Cell Carcinoma", "Acinar cell carcinoma", "Acinic Cell Carcinomas", "Carcinoma, Acinar Cell", "Acinar Cell Carcinomas", "Carcinoma, Acinic Cell", "Carcinomas, Acinic Cell", "Carcinomas, Acinar Cell", "carcinoma of acinar cell", "acinar cell adenocarcinoma", "Acinic cell adenocarcinoma", "Acinar Cell Adenocarcinoma", "Acinic Cell Adenocarcinoma", "acinic cell adenocarcinoma", "Acinar Cell Adenocarcinomas", "Adenocarcinoma, Acinar Cell", "Adenocarcinoma, Acinic Cell", "Acinic Cell Adenocarcinomas", "Adenocarcinomas, Acinic Cell", "Adenocarcinomas, Acinar Cell", "acinar cell carcinoma (diagnosis)", "carcinoma, acinar cell, malignant", "CARCINOMA, ACINAR CELL, MALIGNANT", "Acinar cell carcinoma (morphologic abnormality)", "acinar cell carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acinar cell carcinoma", "shortest_name_length": 4}
{"curie": "UMLS:C5555018", "names": ["AiCM", "Arrhythmia-Induced Cardiomyopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arrhythmia-Induced Cardiomyopathy", "shortest_name_length": 4}
{"curie": "MONDO:0016983", "names": ["HYPOC1", "Bartter syndrome type V", "Bartter syndrome type 5", "HYPERCALCIURIC HYPOCALCEMIA", "Bartter syndrome with hypocalcemia", "HYPOCALCEMIA, AUTOSOMAL DOMINANT 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bartter syndrome with hypocalcemia", "shortest_name_length": 6}
{"curie": "UMLS:C0342342", "names": ["Idiopathic hypoparathyroidism", "Idiopathic Hypoparathyroidism", "idiopathic hypoparathyroidism", "Hypoparathyroidism, Idiopathic", "Hypoparathyroidism, idiopathic", "idiopathic; hypoparathyroidism", "hypoparathyroidism; idiopathic", "Idiopathic hypoparathyroidism (disorder)", "idiopathic hypoparathyroidism (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Idiopathic Hypoparathyroidism", "shortest_name_length": 29}
{"curie": "MONDO:0006407", "names": ["Mesothelial sarcoma", "mesothelial sarcoma", "Fibrous mesothelioma", "fibrous mesothelioma", "sarcoma, mesothelial", "spindled mesothelioma", "mesothelioma; fibrous", "mesothelioma, fibrous", "fibrous; mesothelioma", "Spindled mesothelioma", "Sarcomatoid Mesothelioma", "Sarcomatoid mesothelioma", "sarcomatous mesothelioma", "sarcomatoid mesothelioma", "mesothelioma, sarcomatous", "Fibrous mesothelioma, NOS", "fibrous mesothelial sarcoma", "mesothelial sarcoma, fibrous", "sarcoma, mesothelial, fibrous", "malignant fibrous mesothelioma", "Malignant fibrous mesothelioma", "sarcomatous mesothelial sarcoma", "Fibrous mesothelioma, malignant", "mesothelial sarcoma, sarcomatous", "sarcoma, mesothelial, sarcomatous", "sarcomatoid mesothelioma (morphologic abnormality)", "Sarcomatoid mesothelioma (morphologic abnormality)", "malignant fibrous mesothelioma (morphologic abnormality)", "Fibrous mesothelioma, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sarcomatoid mesothelioma", "shortest_name_length": 19}
{"curie": "MONDO:0010733", "names": ["SPG2", "SPPX2", "Sppx2", "Spastic gait type 2", "spastic gait type 2", "spastic paraplegia 2", "spastic paraplegia type 2", "Spastic paraplegia type 2", "Spastic paraparesis type 2", "spastic paraparesis type 2", "X-linked spastic paraplegia 2", "spastic paraplegia 2, X-linked", "SPASTIC PARAPLEGIA 2, X-LINKED", "Spastic paraplegia 2, X-linked", "hereditary spastic paraplegia 2", "PLP1 hereditary spastic paraplegia", "X-linked spastic paraplegia type 2", "hereditary spastic paraplegia type 2", "SPASTIC PARAPLEGIA 2, X-LINKED (disorder)", "X-linked spastic paraplegia type 2 (disorder)", "spastic paraplegia 2, X-linked, X-linked recessive", "hereditary spastic paraplegia caused by mutation in PLP1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 2", "shortest_name_length": 4}
{"curie": "UMLS:C3899671", "names": ["Cerebellar Anaplastic Astrocytoma", "Childhood Cerebellar Anaplastic Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Cerebellar Anaplastic Astrocytoma", "shortest_name_length": 33}
{"curie": "MONDO:0045003", "names": ["scrotum disease", "disorder scrotum", "scrotal disorder", "scrotum disorder", "Scrotal disorder", "scrotum diseases", "disorders scrotum", "scrotum; disorder", "scrotal disorders", "Disease of scrotum", "disease of scrotum", "Disorder of scrotum", "disorder of scrotum", "Scrotal disorder NOS", "Disease of scrotum, NOS", "DISEASES OF THE SCROTUM", "Disorder of scrotum, NOS", "scrotum disease or disorder", "scrotal disorders (diagnosis)", "Disorder of scrotum (disorder)", "disease or disorder of scrotum", "disease (or disorder); scrotum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scrotal disorder", "shortest_name_length": 15}
{"curie": "UMLS:C1334604", "names": ["Malignant Major Salivary Gland Mixed Tumor", "Malignant Mixed Tumor of Major Salivary Gland", "Malignant Major Salivary Gland Mixed Neoplasm", "Malignant Mixed Neoplasm of Major Salivary Gland", "Malignant Mixed Tumor of the Major Salivary Gland", "Malignant Mixed Neoplasm of the Major Salivary Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Mixed Tumor of the Major Salivary Gland", "shortest_name_length": 42}
{"curie": "MONDO:0001478", "names": ["ANISOMETROPIA", "anisometropia", "Anisometropia", "anisometropia (disease)", "Anisometropia (disorder)", "anisometropia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anisometropia", "shortest_name_length": 13}
{"curie": "UMLS:C1883020", "names": ["Severe Combined Immunodeficiency with Absence of T and B Cells"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Severe Combined Immunodeficiency with Absence of T and B Cells", "shortest_name_length": 62}
{"curie": "UMLS:C2698836", "names": ["Pleomorphic Variant Mantle Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pleomorphic Variant Mantle Cell Lymphoma", "shortest_name_length": 40}
{"curie": "UMLS:C1112466", "names": ["Migrainous Infarction", "Migrainous infarction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Migrainous infarction", "shortest_name_length": 21}
{"curie": "UMLS:C1332298", "names": ["Angiosarcoma NCI Grade 2", "Angiosarcoma NCI Grade II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Angiosarcoma NCI Grade 2", "shortest_name_length": 24}
{"curie": "MONDO:0009919", "names": ["Pseudo-NALD", "pseudo-NALD", "ACOX1 deficiency", "Pseudoadrenoleukodystrophy", "Acyl-CoA oxidase deficiency", "Acyl-coenzyme A oxidase deficiency", "Pseudoneonatal adrenoleukodystrophy", "Peroxisomal acyl-coenzyme A oxidase", "peroxisomal acyl-coenzyme A oxidase", "PSEUDONEONATAL ADRENOLEUKODYSTROPHY", "Pseudo-neonatal adrenoleukodystrophy", "Pseudo-neonatal adrenoleucodystrophy", "pseudo-neonatal adrenoleukodystrophy", "Peroxisomal acyl-CoA oxidase deficiency", "peroxisomal acyl-CoA oxidase deficiency", "PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY", "Peroxisomal Acyl-CoA Oxidase Deficiency", "Peroxisomal ACYL-COA oxidase deficiency", "straight-chain acyl-Coa oxidase deficiency", "Straight-chain acyl-CoA oxidase deficiency", "Straight-chain ACYL-COA oxidase deficiency", "Straight-Chain Acyl-CoA Oxidase Deficiency", "STRAIGHT-CHAIN ACYL-CoA OXIDASE DEFICIENCY", "Acyl-coenzyme A oxidase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisomal acyl-CoA oxidase deficiency", "shortest_name_length": 11}
{"curie": "UMLS:C1335577", "names": ["Pure Erythroid Leukemia in Remission"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pure Erythroid Leukemia in Remission", "shortest_name_length": 36}
{"curie": "MONDO:0021804", "names": ["silicotuberculosis", "Silicotuberculosis", "Silicotuberculoses", "silicotuberculoses", "SILICOTUBERCULOSIS", "Silicotuberculosis (disorder)", "silicotuberculosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "silicotuberculosis", "shortest_name_length": 18}
{"curie": "DOID:5683", "names": ["HBOC Syndrome", "HBOC syndrome", "HBOC Syndromes", "Syndrome, HBOC", "Syndromes, HBOC", "Breast and Ovarian Cancer", "Breast and Ovarian Cancer syndrome", "Hereditary breast and ovarian cancer", "Hereditary Breast and Ovarian Cancer", "familial breast-ovarian cancer syndrome", "hereditary breast ovarian cancer syndrome", "Familial Breast and Ovarian Cancer Syndrome", "Hereditary Breast and Ovarian Cancer syndrome", "Hereditary Breast and Ovarian Cancer Syndrome", "Familial Breast/Ovarian Cancer (BRCA1, BRCA2)", "Hereditary breast and ovarian cancer syndrome", "Hereditary Breast/Ovarian Cancer (BRCA1, BRCA2)", "hereditary breast/ovarian cancer (BRCA1, BRCA2)", "familial breast-ovarian cancer syndrome (diagnosis)", "Hereditary breast and ovarian cancer syndrome (disorder)", "BRCA1/2-Associated Hereditary Breast and Ovarian Cancer Syndrome", "BRCA1- and BRCA2-associated hereditary breast and ovarian cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary breast ovarian cancer syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0010063", "names": ["corneal cerebellar syndrome", "corneal-cerebellar syndrome", "Corneal cerebellar syndrome", "Corneal-Cerebellar Syndrome", "CORNEAL-CEREBELLAR SYNDROME", "Der Kaloustian-Jarudi-Khoury syndrome", "Der Kaloustian Jarudi Khoury syndrome", "Der kaloustian Jarudi Khoury syndrome", "spinocerebellar degeneration corneal dystrophy", "spinocerebellar degeneration and corneal dystrophy", "SPINOCEREBELLAR DEGENERATION AND CORNEAL DYSTROPHY", "Spinocerebellar degeneration and corneal dystrophy", "corneal dystrophy with spinocerebellar Degeneration", "Corneal dystrophy with spinocerebellar degeneration", "CORNEAL DYSTROPHY WITH SPINOCEREBELLAR DEGENERATION", "Spinocerebellar degeneration-corneal dystrophy syndrome", "spinocerebellar degeneration-corneal dystrophy syndrome", "Spinocerebellar degeneration and corneal dystrophy syndrome", "Spinocerebellar degeneration and corneal dystrophy syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal-cerebellar syndrome", "shortest_name_length": 27}
{"curie": "UMLS:C5555102", "names": ["Penile Cutaneous Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Penile Cutaneous Melanoma", "shortest_name_length": 25}
{"curie": "UMLS:C4744358", "names": ["Locally Advanced Unresectable Pancreatic Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Unresectable Pancreatic Adenocarcinoma", "shortest_name_length": 55}
{"curie": "UMLS:C0851536", "names": ["Administration site reaction", "Administration site reactions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Administration site reaction", "shortest_name_length": 28}
{"curie": "UMLS:C4525861", "names": ["Stage IIA Rectal Neuroendocrine Tumor", "Stage IIA Rectal Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Rectal Neuroendocrine Tumor AJCC v8", "shortest_name_length": 37}
{"curie": "MONDO:0100065", "names": ["TH-deficient infantile parkinsonism and motor delay", "tyrosine hydroxylase infantile parkinsonism and motor delay"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "TH-deficient infantile parkinsonism and motor delay", "shortest_name_length": 51}
{"curie": "MONDO:0019008", "names": ["BRIC", "Bric", "Benign recurrent cholestasis", "Summerskill-Walshe-Tygstrup syndrome", "Benign familial recurrent cholestasis", "BENIGN FAMILIAL RECURRENT CHOLESTASIS", "benign familial recurrent cholestasis", "Benign recurrent intrahepatic cholestasis", "Benign Recurrent Intrahepatic Cholestasis", "benign recurrent intrahepatic cholestasis", "cholestasis, benign recurrent intrahepatic", "BRIC - Benign recurrent intrahepatic cholestasis", "benign familial recurrent cholestasis (diagnosis)", "Benign recurrent intrahepatic cholestasis (disorder)", "benign recurrent intrahepatic cholestasis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign recurrent intrahepatic cholestasis", "shortest_name_length": 4}
{"curie": "UMLS:C4744484", "names": ["FT-UMP", "Thyroid Gland Follicular Tumor of Uncertain Malignant Potential", "Thyroid Gland Follicular Neoplasm of Uncertain Malignant Potential"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Follicular Tumor of Uncertain Malignant Potential", "shortest_name_length": 6}
{"curie": "MONDO:0017754", "names": ["inborn disorder of porphyrin metabolism", "disorder of porphyrin and haem metabolism", "inherited disorder of porphyrin metabolism", "Inherited disorder of porphyrin metabolism", "inborn disorder of porphyrin and haem metabolism", "Inherited disorder of porphyrin metabolism (disorder)", "inborn error of porphyrin-containing compound metabolic process", "inborn porphyrin-containing compound metabolic process disorder", "rare inborn error of porphyrin-containing compound metabolic process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of porphyrin metabolism", "shortest_name_length": 39}
{"curie": "MONDO:0005221", "names": ["renal TCC", "Renal urothelial carcinoma", "renal pelvis urothelial cancer", "Renal Pelvis Urothelial Cancer", "Renal transitional cell carcinoma", "Urothelial cancer of renal pelvis", "Transitional renal cell carcinoma", "Renal Pelvis Urothelial Carcinoma", "renal pelvis urothelial carcinoma", "kidney renal pelvis urothelial cancer", "transitional cell carcinoma of kidney", "Transitional cell carcinoma of kidney", "renal pelvis transitional cell carcinoma", "RENAL PELVIS TRANSITIONAL CELL CARCINOMA", "Renal Pelvis Transitional Cell Carcinoma", "Urothelial cell carcinoma of renal Pelvis", "Urothelial Cell Carcinoma of Renal Pelvis", "urothelial cell carcinoma of renal pelvis", "transitional cell carcinoma of renal pelvis", "Transitional Cell Carcinoma of Renal Pelvis", "KIDNEY, PELVIS, PAPILLOMA, TRANSITIONAL CELL", "urothelial cell carcinoma of the renal pelvis", "Urothelial Cell Carcinoma of the Renal Pelvis", "transitional cell carcinoma of the renal pelvis", "Transitional Cell Carcinoma of the Renal Pelvis", "Transitional cell carcinoma of kidney (disorder)", "RENAL CANCER, PELVIS TRANSITIONAL CELL CARCINOMA", "transitional cell carcinoma of kidney (diagnosis)", "transitional cell carcinoma of renal pelvis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal pelvis urothelial carcinoma", "shortest_name_length": 9}
{"curie": "UMLS:C0022594", "names": ["Acquired keratosis", "Keratosis blennorrhagica", "keratosis blennorrhagica", "Keratosis Blennorrhagica", "keratoderma blenorrhagica", "Keratosis Blennorrhagicas", "Blennorrhagica, Keratosis", "Keratoderma blenorrhagica", "Keratoderma blenorrhagicum", "Blennorrhagicas, Keratosis", "Keratoderma blennorrhagicum", "Keratoderma Blennorrhagicum", "keratodermia blennorrhagica", "keratoderma blennorrhagicum", "Keratodermia blennorrhagica", "Reiter's disease of the skin", "Blennorrhagicum, Keratoderma", "Keratoderma Blennorrhagicums", "Blennorrhagicums, Keratoderma", "Acquired keratosis blennorrhagica", "keratosis blennorrhagica (diagnosis)", "Keratoderma blennorrhagicum (disorder)", "Hyperkeratotic skin lesions due to Reiter's disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Keratosis Blennorrhagica", "shortest_name_length": 18}
{"curie": "UMLS:C3266060", "names": ["BOC", "Botryoid Odontogenic Cyst", "Botryoid odontogenic cyst", "Botryoid odontogenic cyst (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Botryoid odontogenic cyst", "shortest_name_length": 3}
{"curie": "MONDO:0014080", "names": ["OSMD", "OSTEOSCLEROTIC METAPHYSEAL DYSPLASIA", "osteosclerotic metaphyseal dysplasia", "Osteosclerotic metaphyseal dysplasia", "Osteosclerotic metaphyseal dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteosclerotic metaphyseal dysplasia", "shortest_name_length": 4}
{"curie": "UMLS:C0553690", "names": ["rind", "RIND", "RIND syndrome", "R.I.N.D. syndrome", "REVERSIBLE ISCHEMIC NEUROLOGIC DEFICIT", "reversible ischemic neurologic deficit", "Reversible ischemic neurological defect", "Reversible ischemic neurological deficit", "Reversible ischaemic neurological defect", "reversible ischemic neurological deficit", "Reversible ischaemic neurological deficit", "RIND - Reversible ischemic neurological defect", "Reversible ischemic neurologic deficit syndrome", "RIND - Reversible ischaemic neurological defect", "Reversible ischaemic neurologic deficit syndrome", "reversible ischemic neurologic deficit (diagnosis)", "Reversible ischemic neurologic deficit (R.I.N.D.) syndrome", "reversible ischemic neurologic deficit (R.I.N.D.) syndrome", "Reversible ischemic neurologic deficit syndrome (disorder)", "Reversible ischaemic neurologic deficit (R.I.N.D.) syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reversible ischemic neurologic deficit (R.I.N.D.) syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0854448", "names": ["Bladder constriction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder constriction", "shortest_name_length": 20}
{"curie": "MONDO:0018756", "names": ["Graves orbitopathy", "thyroid eye disease", "Graves ophthalmopathy", "euthyroid Graves orbitopathy", "euthyroid Graves ophthalmopathy", "Thyroid associated ophthalmopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "euthyroid Graves orbitopathy", "shortest_name_length": 18}
{"curie": "MONDO:0010656", "names": ["MRX", "MRX1", "MRX78", "XLID1", "MRX18", "IQSEC2", "IQSEC2-related epilepsy", "X-linked mental retardation 1", "X-linked mental retardation 78", "Mental Retardation, X-Linked 1", "mental retardation, X-linked 1", "X-linked mental retardation 18", "MENTAL RETARDATION, X-LINKED 1", "Mental Retardation, X-linked 1", "mental retardation, X-linked 18", "mental retardation, X-linked 78", "MENTAL RETARDATION, X-LINKED 18", "MENTAL RETARDATION, X-LINKED 78", "Mental Retardation, X-Linked 78", "X-linked mental retardation 1/78", "X-linked intellectual disability 1", "intellectual disability, X-linked 1", "X-linked intellectual disability 78", "mental retardation, X-linked type 1", "X-linked intellectual disability 1/78", "IQSEC2-related intellectual disability", "X-linked mental retardation 1 (MRX1, XLMR1)", "X-linked non-syndromic intellectual disability", "X-linked mental retardation 18 (MRX18, XLMR18)", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 1", "non-syndromic X-linked intellectual disability 1", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 78", "intellectual developmental disorder, X-linked 1, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 1", "shortest_name_length": 3}
{"curie": "MONDO:0012826", "names": ["IS4", "SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 4", "scoliosis, isolated, susceptibility to, 4", "scoliosis, idiopathic, susceptibility to, 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scoliosis, isolated, susceptibility to, 4", "shortest_name_length": 3}
{"curie": "UMLS:C0267072", "names": ["esophageal dysphagia", "Esophageal Dysphagia", "Esophageal dysphagia", "oesophageal dysphagia", "Oesophageal dysphagia", "Dysphagia, Esophageal", "Esophageal dysphagia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Dysphagia", "shortest_name_length": 20}
{"curie": "UMLS:C0747479", "names": ["PERIDENTAL INFECTION", "infection; peridental", "periodontal infection", "Periodontal infection", "Periodontal Infection", "peridental; infection", "periodontal; infection", "infection; periodontal", "infections periodontal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Periodontal infection", "shortest_name_length": 20}
{"curie": "UMLS:C0751263", "names": ["Learning Disturbance", "LEARNING DISTURBANCE", "Learning Disturbances", "Disturbance, Learning", "Disturbances, Learning"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Learning Disturbance", "shortest_name_length": 20}
{"curie": "UMLS:C0086540", "names": ["American Leishmaniasis", "leishmaniasis; American", "Leishmaniasis, American", "American; leishmaniasis", "New World Leishmaniasis", "Leishmaniasis, New World"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leishmaniasis, New World", "shortest_name_length": 22}
{"curie": "UMLS:C5556683", "names": ["Locally Advanced Glioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Glioma", "shortest_name_length": 23}
{"curie": "UMLS:C0234547", "names": ["drug withdrawal seizure", "Drug withdrawal seizure", "Seizure, drug withdrawal", "Drug withdrawal convulsion", "Drug withdrawal convulsions", "convulsions drug withdrawal", "drug withdrawal with seizure", "drug withdrawal with seizure (diagnosis)", "unspecified substance withdrawal drug with seizure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drug withdrawal convulsions", "shortest_name_length": 23}
{"curie": "MONDO:0007783", "names": ["MHS", "MHS1", "King syndrome", "hyperpyrexia, malignant", "King Denborough syndrome", "King-Denborough syndrome", "hyperthermia of anesthesia", "King-Denborough syndrome, included", "malignant hyperthermia susceptibility 1", "RYR1 malignant hyperthermia of anesthesia", "susceptibility to malignant hyperthermia 1", "Malignant Hyperthermia, Susceptibility To, 1", "Malignant hyperthermia susceptibility type 1", "malignant hyperthermia susceptibility type 1", "malignant hyperthermia, susceptibility to, 1", "MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 1", "malignant hyperthermia, susceptibility to, type 1", "hyperpyrexia, malignant;MH KING syndrome, included", "malignant hyperthermia of anesthesia caused by mutation in RYR1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant hyperthermia, susceptibility to, 1", "shortest_name_length": 3}
{"curie": "MONDO:0001499", "names": ["retroperitoneal lymphoma", "Retroperitoneal Lymphoma", "retroperitoneal space lymphoma", "Primary Retroperitoneal Lymphoma", "primary retroperitoneal lymphoma", "lymphoma of retroperitoneal space", "Lymphoma of retroperitoneal space", "Lymphoma of retroperitoneal space (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retroperitoneal lymphoma", "shortest_name_length": 24}
{"curie": "MONDO:0007341", "names": ["CLEIDORHIZOMELIC SYNDROME", "cleidorhizomelic syndrome", "Cleidorhizomelic syndrome", "cleido rhizomelic syndrome", "Cleido rhizomelic syndrome", "Wallis Zieff Goldblatt syndrome", "Wallis-Zieff-Goldblatt syndrome", "Cleidorhizomelic syndrome (disorder)", "rhizomelic shortness with clavicular defect", "Rhizomelic shortness with clavicular defect", "brachydactyly, enlarged diaphysis, rhizomelic micromelia, short stature and abnormal clavicle"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleidorhizomelic syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0001860", "names": ["FOLATE DEFICIENCY ANEMIA", "Anemia folate deficiency", "Folate Deficiency Anemia", "Folate-deficiency anemia", "Folate deficiency anemia", "anemia folate deficiency", "ANEMIA DEFICIENCY FOLATE", "ANEMIA FOLATE DEFICIENCY", "anemia deficiency folate", "folate deficiency anemia", "folate-deficiency anemia", "Anaemia;folate deficiency", "Folate deficiency anaemia", "Folate-deficiency anaemia", "Anaemia folate deficiency", "folate deficiency anaemia", "anemia; folate deficiency", "anemia; deficiency folate", "folate; deficiency, anemia", "anemia; deficiency, folate", "deficiency; folate, anemia", "deficiency; anemia, folate", "ANEMIA OF FOLATE DEFICIENCY", "ANEMIA FOLIC ACID DEFICIENCY", "Anemia folic acid deficiency", "anemia folic acid deficiency", "folic acid deficiency anemia", "Folic acid deficiency anemia", "anemia; deficiency folic acid", "ANEMIA, FOLIC ACID DEFICIENCY", "folic acid deficiency anaemia", "anemia; folic acid deficiency", "Folic acid deficiency anaemia", "ANAEMIA FOLIC ACID DEFICIENCY", "Anaemia folic acid deficiency", "folic acid; deficiency, anemia", "deficiency; folic acid, anemia", "Folic acid deficiency anemia NOS", "Folate deficiency anemia, unspecified", "Folate-deficient megaloblastic anemia", "Folate deficiency anaemia, unspecified", "Folate-deficient megaloblastic anaemia", "folate-deficient megaloblastic anaemia", "folic acid deficiency anemia (diagnosis)", "Folate or folic acid deficiency anemia NOS", "Megaloblastic anemia due to folate deficiency", "Megaloblastic anaemia due to folate deficiency", "Megaloblastic anemia due to folic acid deficiency", "Megaloblastic anemia due to folate deficiency, NOS", "Megaloblastic anaemia due to folate deficiency, NOS", "Megaloblastic anemia due to folate deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "folic acid deficiency anemia", "shortest_name_length": 24}
{"curie": "UMLS:C3670828", "names": ["Immune-mediated arthritis", "Immune-mediated osteoarthritis", "Immune-mediated arthritis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immune-mediated arthritis", "shortest_name_length": 25}
{"curie": "UMLS:C0346179", "names": ["Hilus Cell Tumor", "Hilus cell tumor", "Hilar cell tumor", "Hilus cell tumour", "Hilar cell tumour", "tumor; hilar cell", "hilar cell; tumor", "Hilar Cell Neoplasm", "[M]Hilar cell tumor", "Hilus Cell Neoplasm", "[M]Hilar cell tumour", "Ovarian Hilar Cell Tumor", "Ovarian Hilus Cell Tumor", "Hilar Cell Tumor of Ovary", "Hilus cell tumor of ovary", "Hilus cell tumour of ovary", "Hilar Cell Tumor of the Ovary", "Hilus cell tumor of ovary (disorder)", "Hilus cell tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hilus cell tumor", "shortest_name_length": 16}
{"curie": "UMLS:C4725819", "names": ["Refractory Malignant Urinary System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Malignant Urinary System Neoplasm", "shortest_name_length": 44}
{"curie": "UMLS:C0268384", "names": ["Andrade syndrome", "Amyloidosis, type I", "ATTRV30M amyloidosis", "TTR amyloid neuropathy", "Portuguese; amyloidosis", "amyloidosis; Portuguese", "AMYLOIDOSIS, NEUROPATHIC", "Amyloid Neuropathy Type 1", "Wohlwill-Andrade Syndrome", "Wohlwill Andrade Syndrome", "ATTRV30M-related amyloidosis", "Neuropathic Amyloid Syndrome", "Neuropathic Amyloid Syndromes", "Amyloid Syndrome, Neuropathic", "Amyloid polyneuropathy type I", "Amyloid Syndromes, Neuropathic", "type I neuropathic amyloidosis", "Corino de Andrade paramyloidosis", "Wohlwill Corino Andrade Syndrome", "Wohlwill-Corino Andrade syndrome", "Wohlwill-Corino Andrade Syndrome", "Transthyretin amyloid neuropathy", "Familial amyloid neuropathy, type I", "Andrade type amyloid polyneuropathy", "Swedish type amyloid polyneuropathy", "Portuguese polyneuritic amyloidosis", "Portuguese Polyneuritic Amyloidoses", "Portuguese Polyneuritic Amyloidosis", "Transthyretin amyloid polyneuropathy", "Japanese type amyloid polyneuropathy", "Polyneuritic Amyloidosis, Portuguese", "Amyloidoses, Portuguese Polyneuritic", "Amyloidosis, Portuguese Polyneuritic", "Polyneuritic Amyloidoses, Portuguese", "Type I Familial Amyloid Polyneuropathy", "Portuguese type amyloid polyneuropathy", "Familial amyloid polyneuropathy type I", "Familial Amyloid Polyneuropathy, Type I", "Familial primary amyloidosis of Andrade", "Amyloid polyneuropathy type I (disorder)", "Familial Amyloid Neuropathy, Andrade Type", "Familial amyloid neuropathy, Andrade type", "type I neuropathic amyloidosis (diagnosis)", "Hereditary neuropathic amyloidosis, type I", "Portuguese Type Familial Amyloid Neuropathy", "Familial Portuguese Polyneuritic Amyloidosis", "Familial amyloid neuropathy, Portuguese type", "Familial Amyloid Neuropathy, Portuguese Type", "Familial amyloid polyneuropathy, 30 Met-for-Val", "Hereditary amyloid polyneuropathy Portuguese type", "Hereditary neuropathic amyloidosis, Portuguese type", "Familial amyloid polyneuropathy, Portuguese-Swedish-Japanese type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Familial Amyloid Neuropathy, Portuguese Type", "shortest_name_length": 16}
{"curie": "MONDO:0019802", "names": ["secondary short bowel syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary short bowel syndrome", "shortest_name_length": 30}
{"curie": "MONDO:0017096", "names": ["FCD type Ia", "isolated focal cortical dysplasia type Ia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated focal cortical dysplasia type Ia", "shortest_name_length": 11}
{"curie": "UMLS:C0497217", "names": ["Other eye disorders", "Other disease of eye", "Other disorders of eye", "Eye/adnexa disease other"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eye/adnexa disease other", "shortest_name_length": 19}
{"curie": "MONDO:0007713", "names": ["Facial hemispasm", "facial hemispasm", "Hemifacial spasm", "hemifacial spasm", "clonic hemifacial spasm", "focal myoclonus of face", "Focal myoclonus of face", "Clonic hemifacial spasm", "Hemifacial Spasm, Familial", "HEMIFACIAL SPASM, FAMILIAL", "hemifacial spasm, familial", "Clonic hemifacial spasm (finding)", "clonic hemifacial spasm (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "clonic hemifacial spasm", "shortest_name_length": 16}
{"curie": "MONDO:0009528", "names": ["CRD", "ANDD", "CMRD", "Anderson disease", "anderson disease", "ANDERSON DISEASE", "Anderson Disease", "disease anderson", "andersons disease", "Anderson Syndrome", "Anderson syndrome", "anderson's disease", "andersons syndrome", "Anderson's disease", "chylomicron retention disease", "Chylomicron retention disease", "CHYLOMICRON RETENTION DISEASE", "Anderson's disease (diagnosis)", "Lipid transport defect of intestine", "LIPID TRANSPORT DEFECT OF INTESTINE", "lipid Transport defect of intestine", "Chylomicron retention disease (disorder)", "chylomicron retention disease (diagnosis)", "hypobetalipoproteinemia with accumulation of apolipoprotein B-like Protein in intestinal cells", "Hypobetalipoproteinemia with Accumulation of Apolipoprotein B-Like Protein In Intestinal Cells", "hypobetalipoproteinemia with accumulation of apolipoprotein B-like protein in intestinal cells", "HYPOBETALIPOPROTEINEMIA WITH ACCUMULATION OF APOLIPOPROTEIN B-LIKE PROTEIN IN INTESTINAL CELLS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chylomicron retention disease", "shortest_name_length": 3}
{"curie": "MONDO:0019817", "names": ["congenital mitral valve insufficiency and/or stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital mitral valve insufficiency and/or stenosis", "shortest_name_length": 53}
{"curie": "MONDO:0009335", "names": ["AHUS1", "AHUS, SUSCEPTIBILITY TO, 1", "Ahus, susceptibility to, 1", "Typical hemolytic uremic syndrome", "hemolytic uremic syndrome, typical", "HEMOLYTIC UREMIC SYNDROME, TYPICAL", "hemolytic uremic syndrome, atypical, susceptibility to", "susceptibility to atypical hemolytic uremic syndrome 1", "HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1", "hemolytic uremic syndrome, atypical, susceptibility to, 1", "hemolytic uremic syndrome, atypical, susceptibility to, type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemolytic uremic syndrome, atypical, susceptibility to, 1", "shortest_name_length": 5}
{"curie": "MONDO:0009818", "names": ["OPTB3", "Mixed RTA", "mixed RTA", "Marble brain disease", "marble brain disease", "MARBLE BRAIN DISEASE", "Marble Brain Disease", "GUIBAUD-VAINSEL SYNDROME", "Guibaud Vainsel syndrome", "Guibaud-Vainsel syndrome", "Guibaud-Vainsel Syndrome", "CA2 osteopetrosis (disease)", "mixed renal tubular acidosis", "Mixed renal tubular acidosis", "Renal tubular acidosis type 3", "renal tubular acidosis type 3", "carbonic anhydrase 2 deficiency", "Carbonic anhydrase 2 deficiency", "Carbonic Anhydrase II Deficiency", "carbonic anhydrase II deficiency", "Carbonic anhydrase II deficiency", "CARBONIC ANHYDRASE II DEFICIENCY", "osteopetrosis autosomal recessive 3", "autosomal recessive osteopetrosis 3", "Autosomal Recessive Osteopetrosis 3", "OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3", "Osteopetrosis, Autosomal Recessive 3", "osteopetrosis, autosomal recessive 3", "autosomal recessive osteopetrosis type 3", "Autosomal Recessive Osteopetrosis, Type 3", "Autosomal Recessive osteopetrosis, type 3", "OSTEOPETROSIS WITH RENAL TUBULAR ACIDOSIS", "Osteopetrosis with renal tubular acidosis", "osteopetrosis, autosomal recessive type 3", "osteopetrosis with renal tubular acidosis", "Osteopetrosis with Renal Tubular Acidosis", "CA2 - Osteopetrosis with renal tubular acidosis", "osteopetrosis (disease) caused by mutation in CA2", "Osteopetrosis with renal tubular acidosis (disorder)", "autosomal recessive osteopetrosis 3 with renal tubular acidosis", "osteopetrosis, autosomal recessive 3, with renal tubular acidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive osteopetrosis 3", "shortest_name_length": 5}
{"curie": "UMLS:C3639954", "names": ["CAVD, Unbalanced", "Complete AV Canal Defect Unbalanced", "Complete unbalanced atrioventricular canal defect", "Complete Atrioventricular Canal Defect Unbalanced", "Complete Atrioventricular Canal Defect (Unbalanced)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Complete unbalanced atrioventricular canal defect", "shortest_name_length": 16}
{"curie": "MONDO:0005766", "names": ["Fungi lung disease", "Fungal Lung Disease", "fungal lung disease", "lung disease, fungal", "fungal lung diseases", "Fungal Lung Diseases", "Lung Disease, Fungal", "diseases fungal lungs", "Lung Diseases, Fungal", "Lungs--Diseases, Fungal", "Pulmonary Fungal Disease", "pulmonary fungal disease", "Fungal Disease, Pulmonary", "Fungi caused lung disease", "Pulmonary Fungal Diseases", "fungal disease, pulmonary", "pulmonary fungal diseases", "fungal diseases, pulmonary", "pulmonary fungal infection", "Pulmonary Fungal Infection", "Fungal Diseases, Pulmonary", "fungal infection, pulmonary", "Fungal Infection, Pulmonary", "Pulmonary Fungal Infections", "pulmonary fungal infections", "Fungal Infections, Pulmonary", "fungal infections, pulmonary", "fungal lung infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fungal lung infectious disease", "shortest_name_length": 18}
{"curie": "MONDO:0000677", "names": ["semantic agnosia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "semantic agnosia", "shortest_name_length": 16}
{"curie": "UMLS:C0274285", "names": ["accidental hypothermia", "Accidental hypothermia", "Accidental Hypothermia", "Hypothermia, Accidental", "Accidental Hypothermias", "Hypothermias, Accidental", "Hypothermia - accidental", "Hypothermia - accidental (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypothermia, Accidental", "shortest_name_length": 22}
{"curie": "UMLS:C0232197", "names": ["fibrillate", "Fibrillated", "Fibrillation", "FIBRILLATION", "fibrillating", "fibrillation", "Fibrillations", "fibrillations", "Fibrillation, NOS", "Heart Fibrillation", "heart fibrillation", "heart; fibrillation", "fibrillation; heart", "Cardiac fibrillation", "Fibrillation cardiac", "FIBRILLATION CARDIAC", "Fibrillation (Heart)", "cardiac fibrillation", "cardiac; fibrillation", "fibrillation; cardiac", "Fibrillation (disorder)", "FIBRILLATION CARDIAC NOS", "fibrillation (diagnosis)", "Fibrillation cardiac NOS", "Cardiac fibrillation NOS", "Cardiac fibrillation, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fibrillation", "shortest_name_length": 10}
{"curie": "MONDO:0001601", "names": ["Ovale malaria", "ovale malaria", "malaria; ovale", "Malaria, ovale", "ovale; malarial", "Plasmodium; ovale", "Ovale tertian malaria", "Plasmodium ovale malaria", "Ovale malaria (disorder)", "malaria; Plasmodium ovale", "Malariaby Plasmodium ovale", "Malaria by Plasmodium ovale", "malaria due to plasmodium ovale", "Malaria fever by Plasmodium ovale", "malaria due to plasmodium ovale (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Plasmodium ovale malaria", "shortest_name_length": 13}
{"curie": "UMLS:C5420847", "names": ["Retinal Pigment Epithelium Adenocarcinoma", "Adenocarcinoma of the Retinal Pigment Epithelium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retinal Pigment Epithelium Adenocarcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0003337", "names": ["Acute Hemorrhagic Encephalitis", "acute hemorrhagic encephalitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute hemorrhagic encephalitis", "shortest_name_length": 30}
{"curie": "MONDO:0001309", "names": ["nerve iii palsy", "III nerve palsy", "iii nerve palsy", "3rd nerve palsy", "oculomotor palsy", "third nerve palsy", "Third-Nerve Palsy", "Third Nerve Palsy", "Third nerve palsy", "IIIrd nerve palsy", "Palsy, Third-Nerve", "OCULOMOTOR PARESIS", "Oculomotor paresis", "nerve palsies third", "Third nerve paresis", "Third-Nerve Palsies", "IIIrd nerve paresis", "THIRD NERVE PARALYSIS", "Oculomotor neuropathy", "third nerve paralysis", "Third nerve paralysis", "IIIrd nerve paralysis", "Third Nerve Paralysis", "Oculomotor Neuropathy", "Third-Nerve Paralyses", "IIIrd nerve Paralysis", "IIIrd Nerve Paralysis", "Third-Nerve Paralysis", "Oculomotor Nerve Palsy", "Oculomotor nerve palsy", "Cyclic III nerve palsy", "oculomotor nerve palsy", "Paralysis, Third-Nerve", "Neuropathy, Oculomotor", "Nerve Palsy, Oculomotor", "Cranial Nerve III Palsy", "Oculomotor Neuropathies", "Palsy, Oculomotor Nerve", "Cranial nerve palsy III", "Oculomotor Nerve Disease", "Oculomotor Nerve Palsies", "Oculomotor nerve paresis", "third cranial nerve palsy", "Oculomotor Nerve Disorder", "Nerve Disease, Oculomotor", "Oculomotor Nerve Diseases", "Third Cranial Nerve Palsy", "Nerve Disorder, Oculomotor", "oculomotor nerve paralysis", "Oculomotor Nerve Disorders", "Oculomotor nerve paralysis", "n.oculomotorius; paralysis", "OCULOMOTOR NERVE PARALYSIS", "Oculomotor Nerve Paralysis", "Oculomotor Nerve Paralyses", "Cranial Nerve III Diseases", "Cranial third nerve paresis", "Paralysis, Oculomotor Nerve", "paralysis; oculomotor nerve", "CRANIAL THIRD NERVE PARESIS", "Nerve Paralysis, Oculomotor", "Palsy;III nerve (oculomotor)", "Third Cranial Nerve Diseases", "Third cranial nerve weakness", "third cranial nerve paralysis", "paralysis third cranial nerve", "cranial nerve paralysis third", "Third cranial nerve paralysis", "CRANIAL THIRD NERVE PARALYSIS", "Cranial third nerve paralysis", "Third [oculomotor] nerve palsy", "paralysis; cranial nerve, third", "Third cranial nerve paralysis, NOS", "oculomotor nerve cranial nerve palsy", "third cranial nerve palsy (diagnosis)", "Third cranial nerve weakness (disorder)", "cranial nerve palsy of oculomotor nerve"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculomotor nerve paralysis", "shortest_name_length": 15}
{"curie": "MONDO:0013401", "names": ["CPSQ4", "SPG51", "CPSQ4, FORMERLY", "hereditary spastic paraplegia 51", "AP4E1 hereditary spastic paraplegia", "hereditary spastic paraplegia type 51", "spastic quadriplegic cerebral palsy 4", "cerebral palsy, spastic quadriplegic, 4", "autosomal dominant spastic paraplegia 51", "spastic paraplegia 51, autosomal recessive", "SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE", "CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 4, FORMERLY", "cerebral palsy, spastic quadriplegic, 4, formerly", "hereditary spastic paraplegia caused by mutation in AP4E1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 51", "shortest_name_length": 5}
{"curie": "MONDO:0013230", "names": ["HWE2", "hot water epilepsy 2", "Hot Water Epilepsy, 2", "EPILEPSY, HOT WATER, 2", "epilepsy, hot water, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, hot water, 2", "shortest_name_length": 4}
{"curie": "UMLS:C5237824", "names": ["Advanced Gastric Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Gastric Adenocarcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0019898", "names": ["distal monosomy 14q", "distal deletion 14q", "telomeric deletion 14q", "distal monosomy type 14q"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal monosomy 14q", "shortest_name_length": 19}
{"curie": "UMLS:C4528548", "names": ["Breast Cancer by AJCC v8 Stage", "Breast Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Cancer by AJCC v8 Stage", "shortest_name_length": 30}
{"curie": "MONDO:0018586", "names": ["NAE", "necrolytic acral erythema", "Necrolytic acral erythema", "Necrolytic acral erythema (disorder)", "zinc-responsive necrolytic acral erythema", "Zinc-responsive necrolytic acral erythema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "zinc-responsive necrolytic acral erythema", "shortest_name_length": 3}
{"curie": "MONDO:0011864", "names": ["CVID1", "immunodeficiency, common variable", "common variable immunodeficiency 1", "IMMUNODEFICIENCY, COMMON VARIABLE, 1", "immunodeficiency, common variable, 1", "ANTIBODY DEFICIENCY DUE TO ICOS DEFECT", "antibody deficiency due to Icos defect", "immunodeficiency, common variable, type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency, common variable, 1", "shortest_name_length": 5}
{"curie": "MONDO:0018204", "names": ["Dup(20)(q11.2)", "dup(20)(q11.2)", "20q11.2 microduplication syndrome", "20q11.2 microduplication syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "20q11.2 microduplication syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C0856026", "names": ["Splenic Marginal Zone Lymphoma Stage III", "Splenic marginal zone lymphoma stage III", "Stage III Splenic Marginal Zone Lymphoma", "Stage III Splenic Marginal Zone B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Splenic marginal zone lymphoma stage III", "shortest_name_length": 40}
{"curie": "MONDO:0012500", "names": ["CHBL1", "chilblain lupus", "chilblain lupus 1", "TREX1 chilblain lupus", "chilblain lupus type 1", "chilblain lupus caused by mutation in TREX1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chilblain lupus 1", "shortest_name_length": 5}
{"curie": "UMLS:C4683605", "names": ["Lugano Classification Adult Hodgkin Lymphoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Adult Hodgkin Lymphoma by AJCC v8 Stage", "shortest_name_length": 61}
{"curie": "MONDO:0019238", "names": ["pyrimidine metabolic disorder", "disorder of pyrimidine metabolism", "inborn disorder of pyrimidine metabolism", "inborn pyrimidine nucleobase metabolic process disorder", "inborn error of pyrimidine nucleobase metabolic process", "rare inborn error of pyrimidine nucleobase metabolic process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of pyrimidine metabolism", "shortest_name_length": 29}
{"curie": "UMLS:C4743689", "names": ["Transplant-Related Squamous Cell Carcinoma", "Transplant-Associated Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transplant-Related Squamous Cell Carcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0016493", "names": ["variant of GBS", "variant of Guillain-Barre syndrome", "variant of Guillain-Barré syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "variant of Guillain-Barre syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0010269", "names": ["coat disease", "Coat Disease", "Coats disease", "COATS DISEASE", "coats disease", "Coats Disease", "coat syndrome", "Coats' disease", "Coats' Disease", "coats' disease", "Coat's disease", "Coats syndrome", "coat's disease", "coats syndrome", "Coats' syndrome", "coats's disease", "Coat's syndrome", "coat's syndrome", "exudative retinopathy", "Exudative retinopathy", "Retinal Telangiectases", "Retinal Telangiectasis", "retinal telangiectasis", "RETINAL TELANGIECTASIS", "Retinal telangiectasis", "Leber miliary aneurysm", "Telangiectasis, Retinal", "Telangiectases, Retinal", "Leber's miliary aneurysms", "Coats' disease (disorder)", "Miliary aneurysms of retina", "Coats' syndrome (diagnosis)", "Exudative retinopathy (disorder)", "congenital retinal telangiectasia", "Progressive exudative retinopathy", "Congenital retinal telangiectasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Coats disease", "shortest_name_length": 12}
{"curie": "MONDO:0006391", "names": ["pyloric gland adenoma", "Pyloric Gland Adenoma", "Gastric Pyloric Gland Adenoma", "pyloric gastric gland adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyloric gland adenoma", "shortest_name_length": 21}
{"curie": "MONDO:0010984", "names": ["USH1D", "Usher syndrome type 1D", "Usher syndrome type ID", "USHER syndrome, type ID", "Usher syndrome, type 1D", "Usher Syndrome, Type ID", "USHER SYNDROME, TYPE ID", "USH1D/F, CDH23/PCDH15, DIGENIC", "Ush1D/F, Cdh23/Pcdh15, digenic", "Usher syndrome, type 1D/F digenic", "Usher syndrome, type Id/F, Cdh23/Pcdh15, digenic", "USHER SYNDROME, TYPE ID/F, CDH23/PCDH15, DIGENIC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Usher syndrome type 1D", "shortest_name_length": 5}
{"curie": "MONDO:0011123", "names": ["T1D15", "IDDM15", "type 1 diabetes mellitus 15", "TYPE 1 DIABETES MELLITUS 15", "insulin-dependent diabetes mellitus 15", "INSULIN-DEPENDENT DIABETES MELLITUS 15", "Insulin-Dependent Diabetes Mellitus 15", "Diabetes Mellitus, Insulin-Dependent, 15", "DIABETES MELLITUS, INSULIN-DEPENDENT, 15", "diabetes mellitus, insulin-dependent, 15"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type 1 diabetes mellitus 15", "shortest_name_length": 5}
{"curie": "MONDO:0015150", "names": ["Complex HSP", "Complex SPG", "complicated HSP", "Complicated SPG", "Complicated HSP", "complicated SPG", "Complex familial spastic paraplegia", "complex hereditary spastic paraplegia", "Complex hereditary spastic paraplegia", "syndromic hereditary spastic paraplegia", "Complicated familial spastic paraplegia", "complicated familial spastic paraplegia", "complicated hereditary spastic paraplegia", "Complicated hereditary spastic paraplegia", "Complicated hereditary spastic paraplegia (disorder)", "syndrome associated with hereditary spastic paraplegia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complex hereditary spastic paraplegia", "shortest_name_length": 11}
{"curie": "UMLS:C1710632", "names": ["rupture; vessel", "vessels; rupture", "Rupture of Vessel", "Vessel perforation", "Blood Vessel Rupture", "Perforation of Vessels", "Blood Vessel Perforation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vessel perforation", "shortest_name_length": 15}
{"curie": "MONDO:0007288", "names": ["CTPA", "CTPP", "Arcc2", "CTPP1", "ARCC2", "CTRCT6", "EPHA2 cataract (disease)", "cataract 6 multiple types", "cataract 6, multiple types", "posterior polar cataract 1", "CATARACT 6, MULTIPLE TYPES", "Posterior polar cataract, 1", "CATARACT, POSTERIOR POLAR, 1", "cataract, posterior polar, 1", "Cataract, posterior polar, 1", "age related cortical cataract 2", "CATARACT, AGE-RELATED CORTICAL, 2", "cataract, age-related cortical, 2", "Cataract, Age-Related Cortical, 2", "cataract (disease) caused by mutation in EPHA2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 6 multiple types", "shortest_name_length": 4}
{"curie": "UMLS:C4727008", "names": ["Unresectable Synovial Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Synovial Sarcoma", "shortest_name_length": 29}
{"curie": "UMLS:C1334935", "names": ["Neoplasm by Special Category"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplasm by Special Category", "shortest_name_length": 28}
{"curie": "MONDO:0003037", "names": ["Hair thin", "Hair scanty", "Scanty hair", "Sparse hair", "sparse hair", "HYPOTRICHOSIS", "Hypotrichoses", "Hair thinning", "Hypotrichosis", "hypotrichosis", "Sparse, thin hair", "Hypotrichosis NOS", "Thin, sparse hair", "Hypotrichosis, NOS", "the hair was sparse", "Marked hypotrichosis", "Decreased hair growth", "Sparse hair (finding)", "Hair growth decreased", "Congenital hypotrichia", "Sparse hair since birth", "Hypotrichosis congenita", "Congenital hypotrichosis", "Hypotrichosis (disorder)", "hypotrichosis; congenital", "congenital; hypotrichosis", "Decreased hair growth on body", "sparse hair (physical finding)", "Decreased hair growth (finding)", "Hair growth function, decreased", "Congenital hypotrichia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotrichosis", "shortest_name_length": 9}
{"curie": "UMLS:C4521490", "names": ["Stage III Liver Cancer", "Stage III Adult Liver Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Adult Liver Cancer AJCC v7", "shortest_name_length": 22}
{"curie": "UMLS:C5206559", "names": ["Refractory Myelofibrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Myelofibrosis", "shortest_name_length": 24}
{"curie": "MONDO:0018504", "names": ["anaplastic gastric carcinoma", "Anaplastic Gastric Carcinoma", "anaplastic carcinoma of stomach", "Anaplastic Carcinoma of Stomach", "Gastric undifferentiated carcinoma", "Undifferentiated gastric carcinoma", "Undifferentiated Gastric Carcinoma", "undifferentiated gastric carcinoma", "Gastric Undifferentiated Carcinoma", "stomach undifferentiated carcinoma", "anaplastic carcinoma of the stomach", "Anaplastic Carcinoma of the Stomach", "undifferentiated carcinoma of stomach", "Undifferentiated Carcinoma of Stomach", "Undifferentiated carcinoma of stomach", "undifferentiated stomach adenocarcinoma", "Undifferentiated Gastric (Stomach) Cancer", "Undifferentiated Carcinoma of the Stomach", "undifferentiated carcinoma of the stomach", "undifferentiated gastric (stomach) cancer", "anaplastic carcinoma of stomach (diagnosis)", "Undifferentiated carcinoma of stomach (disorder)", "undifferentiated carcinoma of stomach (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "undifferentiated carcinoma of stomach", "shortest_name_length": 28}
{"curie": "MONDO:0014367", "names": ["AGS7", "AICARDI-GOUTIERES SYNDROME 7", "Aicardi-Goutieres Syndrome 7", "Aicardi-Goutieres syndrome 7", "IFIH1 Aicardi-Goutieres syndrome", "Aicardi-Goutieres syndrome type 7", "Aicardi-Goutieres syndrome caused by mutation in IFIH1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aicardi-Goutieres syndrome 7", "shortest_name_length": 4}
{"curie": "MONDO:0016413", "names": ["congenital hypothyroidism due to maternal intake of antithyroid drugs"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital hypothyroidism due to maternal intake of antithyroid drugs", "shortest_name_length": 69}
{"curie": "MONDO:0003171", "names": ["pineal astrocytoma", "Pineal Astrocytoma", "pineal body astrocytoma", "Pineal Astrocytic tumor", "pineal astrocytic tumor", "pineal gland astrocytoma", "Pineal Gland Astrocytoma", "Astrocytoma of Pineal Gland", "astrocytoma of pineal gland", "astrocytoma of the pineal gland", "Astrocytoma of the Pineal Gland", "pineal body astrocytoma (excluding glioblastoma)", "astrocytoma (excluding glioblastoma) of pineal body"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pineal gland astrocytoma", "shortest_name_length": 18}
{"curie": "UMLS:C2981631", "names": ["Stage IIIB Gallbladder Cancer", "Stage IIIB Gallbladder Cancer AJCC v7", "Stage IIIB Gallbladder Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Gallbladder Cancer AJCC v7", "shortest_name_length": 29}
{"curie": "MONDO:0700085", "names": ["pentasomy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pentasomy", "shortest_name_length": 9}
{"curie": "MONDO:0021260", "names": ["sensory ganglionopathy", "sensory ganglion disease", "disease of sensory ganglion", "disorder of sensory ganglion", "sensory ganglion disease or disorder", "disease or disorder of sensory ganglion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sensory ganglionopathy", "shortest_name_length": 22}
{"curie": "UMLS:C4553790", "names": ["0a", "Stage 0a Bladder Cancer", "stage 0a bladder cancer", "Stage 0a Bladder Cancer AJCC v8", "stage 0a bladder cancer AJCC v8", "stage 0a bladder carcinoma AJCC v8", "Stage 0a Bladder Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0a Bladder Cancer AJCC v8", "shortest_name_length": 2}
{"curie": "MONDO:0014235", "names": ["chromosome 22q13 duplication syndrome", "CHROMOSOME 22q13 DUPLICATION SYNDROME", "chromosome 22q13 duplication syndrome, isolated cases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 22q13 duplication syndrome", "shortest_name_length": 37}
{"curie": "MONDO:0003182", "names": ["anterior horn disorder", "anterior horn cell disease", "ventral horn of spinal cord disease", "disease of ventral horn of spinal cord", "disorder of ventral horn of spinal cord", "ventral horn of spinal cord disease or disorder", "disease or disorder of ventral horn of spinal cord"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anterior horn disorder", "shortest_name_length": 22}
{"curie": "UMLS:C2211016", "names": ["Mediastinal Follicular Dendritic Cell Sarcoma", "follicular dendritic cell sarcoma of mediastinum", "Follicular Dendritic Cell Sarcoma of the Mediastinum", "follicular dendritic cell sarcoma of mediastinum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "follicular dendritic cell sarcoma of mediastinum", "shortest_name_length": 45}
{"curie": "MONDO:0008857", "names": ["Beemer Ertbruggen syndrome", "Beemer-Ertbruggen syndrome", "BEEMER LETHAL MALFORMATION SYNDROME", "Beemer lethal malformation syndrome", "hydrocephalus, cardiac malformation, dense bones, etc", "hydrocephalus, Cardiac malformation, dense bones, etc.", "Hydrocephalus, cardiac malformation, dense bone syndrome", "Lethal hydrocephalus-cardiac malformation-dense bones syndrome", "lethal hydrocephalus-cardiac malformation-dense bones syndrome", "Hydrocephalus, cardiac malformation, dense bone syndrome (disorder)", "HYDROCEPHALUS, CARDIAC MALFORMATION, DENSE BONES, GENITAL ANOMALIES, THROMBOCYTOPENIA, AND DYSMORPHIC FACIES", "peculiar facial appearance, hydrocephalus, double-outlet right ventricle, genital anomalies and dense bones with lethal outcome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Beemer-Ertbruggen syndrome", "shortest_name_length": 26}
{"curie": "MONDO:0033043", "names": ["SPAX8", "spastic ataxia 8", "SPAX8 - spastic ataxia 8", "NKX6-2-related autosomal recessive hypomyelinating leukodystrophy", "NKX6-2-related autosomal recessive hypomyelinating leucodystrophy", "NK6 homeobox 2-related autosomal recessive hypomyelinating leukodystrophy", "NK6 homeobox 2-related autosomal recessive hypomyelinating leucodystrophy", "spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy", "SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY", "Autosomal recessive hypomyelinating leukodystrophy-progressive spastic ataxia", "Autosomal recessive hypomyelinating leukodystrophy, progressive spastic ataxia", "Autosomal recessive hypomyelinating leucodystrophy, progressive spastic ataxia", "NK6 homeobox 2-related autosomal recessive hypomyelinating leukodystrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy", "shortest_name_length": 5}
{"curie": "MONDO:0032677", "names": ["LIS9", "LISSENCEPHALY 9 WITH COMPLEX BRAINSTEM MALFORMATION", "lissencephaly 9 with complex brainstem malformation", "Posterior-predominant lissencephaly-broad flat pons and medulla-midline crossing defects syndrome", "posterior-predominant lissencephaly-broad flat pons and medulla-midline crossing defects syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lissencephaly 9 with complex brainstem malformation", "shortest_name_length": 4}
{"curie": "UMLS:C0861725", "names": ["Stage 0 Oropharynx Epidermoid Carcinoma", "Oropharynx Epidermoid Carcinoma in situ", "Oropharynx Squamous Cell Carcinoma in situ", "Stage 0 Epidermoid Carcinoma of Oropharynx", "Oropharyngeal Epidermoid Carcinoma in situ", "Stage 0 Oropharyngeal Epidermoid Carcinoma", "Stage 0 Oropharynx Squamous Cell Carcinoma", "Epidermoid Carcinoma in situ of Oropharynx", "Oropharyngeal Squamous Cell Carcinoma in situ", "Stage 0 Oropharyngeal Squamous Cell Carcinoma", "Oropharyngeal squamous cell carcinoma stage 0", "Stage 0 Squamous Cell Carcinoma of Oropharynx", "Squamous Cell Carcinoma in situ of Oropharynx", "Epidermoid Carcinoma in situ of the Oropharynx", "Stage 0 Epidermoid Carcinoma of the Oropharynx", "Stage 0 Oropharyngeal Throat Squamous Cell Cancer", "Squamous Cell Carcinoma in situ of the Oropharynx", "Stage 0 Squamous Cell Carcinoma of the Oropharynx", "Stage 0 Oropharyngeal Squamous Cell Carcinoma AJCC v6", "Stage 0 Oropharyngeal Squamous Cell Carcinoma AJCC v7", "Stage 0 Oropharyngeal Squamous Cell Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Oropharyngeal Squamous Cell Carcinoma AJCC v6 and v7", "shortest_name_length": 39}
{"curie": "UMLS:C3272651", "names": ["Tobacco Induced Hyperparakeratosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tobacco Induced Hyperparakeratosis", "shortest_name_length": 34}
{"curie": "MONDO:0005009", "names": ["chf", "ccf", "CHF", "Weak heart", "weak heart", "weak; heart", "hearts weak", "Heart Failure", "Failure;heart", "HEART FAILURE", "heart failure", "FAILURE HEART", "Failure heart", "Heart failure", "failures heart", "heart failures", "failure; heart", "Weakness;heart", "heart weakness", "Heart failures", "Cardiac failure", "failure cardiac", "cardiac failure", "heart; weakness", "Weak heart, NOS", "CARDIAC FAILURE", "Failure;cardiac", "Cardiac Failure", "Cardiac failures", "cardiac failures", "cardiac; failure", "heart weaknesses", "failure; cardiac", "congestive; heart", "Heart failure NOS", "heart; congestive", "HF - Heart failure", "Heart failure, NOS", "myocardial failure", "Cardiac failure NOS", "HEART FAILURE (NOS)", "Heart insufficiency", "insufficiency heart", "Heart failure (NOS)", "heart insufficiency", "Cardiac failure, NOS", "insufficiency; heart", "heart; insufficiency", "chronic failure heart", "insufficiency cardiac", "CARDIAC INSUFFICIENCY", "cardiac insufficiency", "Insufficiency;cardiac", "chronic heart failure", "Cardiac failure (NOS)", "Chronic heart failure", "Insufficiency cardiac", "Cardiac insufficiency", "INSUFFICIENCY CARDIAC", "cardiac; insufficiency", "insufficiency; cardiac", "Heart failure, chronic", "Cardiac function failed", "Cardiac failure chronic", "chronic cardiac failure", "cardiac failure chronic", "Myocardial failure, NOS", "CARDIAC FAILURE CHRONIC", "heart congestive failure", "congestive heart disease", "FAILURE HEART CONGESTIVE", "disease congestive heart", "congestive heart failure", "Failure heart congestive", "Congestive heart disease", "failure congestive heart", "congestive disease heart", "heart failure congestive", "Congestive heart failure", "Congestive Heart Failure", "Heart failure (disorder)", "CONGESTIVE HEART FAILURE", "congestive failure heart", "Cardiac function failure", "HEART FAILURE, CONGESTIVE", "heart failure; congestive", "Heart Failure, Congestive", "heart failure, congestive", "congestive failures heart", "congestive failure hearts", "Heart failure, congestive", "failure, congestive heart", "congestive diseases heart", "Failure;congestive cardiac", "congestive cardiac failure", "failure; heart, congestive", "Cardiac failure congestive", "Congestive cardiac failure", "cardiac congestive failure", "Heart failure, unspecified", "cardiac failure congestive", "CARDIAC FAILURE CONGESTIVE", "Cardiac Failure Congestive", "heart; disease, congestive", "cardiac failure (diagnosis)", "cardiac failure, congestive", "Cardiac failure, congestive", "Congestive heart failure NOS", "congestive heart failure chf", "CHF (congestive heart failure)", "congestive heart failure (CHF)", "CHF - Congestive heart failure", "Congestive heart failure (CHF)", "Congestive Heart Failure (CHF)", "CCF - Congestive cardiac failure", "Chronic heart failure (disorder)", "chronic cardiac failure (diagnosis)", "Congestive heart failure (disorder)", "congestive heart failure (diagnosis)", "Congestive heart failure, unspecified", "Heart Failure/Congestive Heart Failure", "HEART FAILURE AND OTHER FUNCTIONAL DISORDERS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congestive heart failure", "shortest_name_length": 3}
{"curie": "UMLS:C1405128", "names": ["pleural fistula", "Pleural Fistula", "pleura; fistula", "Pleural fistula", "fistula; pleural", "Fistula, pleural"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pleural fistula", "shortest_name_length": 15}
{"curie": "MONDO:0016851", "names": ["UPD(X)mat", "maternal uniparental disomy of chromosome X", "maternal uniparental disomy of chromosome type X"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maternal uniparental disomy of chromosome X", "shortest_name_length": 9}
{"curie": "UMLS:C0752097", "names": ["Autosomal Dominant Juvenile Parkinsonism", "Juvenile Parkinsonism, Autosomal Dominant", "Parkinsonism, Juvenile, Autosomal Dominant", "Autosomal Dominant Juvenile Parkinson Disease", "Juvenile Parkinson Disease, Autosomal Dominant", "Parkinson Disease, Autosomal Dominant. Juvenile", "Parkinson Disease, Juvenile, Autosomal Dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Autosomal Dominant Juvenile Parkinson Disease", "shortest_name_length": 40}
{"curie": "MONDO:0008223", "names": ["HKPP", "HOKPP", "HYPOPP", "HypoPP", "HYPOKPP", "Westphal disease", "Westphall disease", "Westphall Disease", "Periodic paralysis I", "periodic paralysis I", "familial periodic paralysis", "Hypokalemic periodic paralysis", "hypokalemic paralysis periodic", "periodic hypokalemic paralysis", "Hypokalemic Periodic Paralysis", "Periodic Paralysis Hypokalemic", "hypokalemic periodic paralysis", "Periodic Paralysis- Hypokalemic", "Paralysis, Hypokalemic Periodic", "hypokalaemic periodic paralysis", "periodic hypokalaemic paralysis", "PERIODIC PARALYSIS, HYPOKALEMIC", "hypokalaemic paralysis periodic", "Periodic Paralysis, Hypokalemic", "Hypokalaemic periodic paralysis", "Periodic Paralysis- Hypokalemics", "HOKPP - hypokalemic periodic paralysis", "Primary Hypokalemic Periodic Paralysis", "hypokalemic familial periodic paralysis", "HOKPP - hypokalaemic periodic paralysis", "hypokalemic periodic paralysis syndrome", "familial hypokalemic periodic paralysis", "Hypokalemic familial periodic paralysis", "Familial Hypokalemic Periodic Paralysis", "Familial hypokalemic periodic paralysis", "Hypokalemic Periodic Paralysis, Familial", "Familial hypokalaemic periodic paralysis", "Hypokalemic periodic paralysis (familial)", "Hypokalemic periodic paralysis (diagnosis)", "FAMILIAL PERIODIC PARALYSIS HYPOKALEMIC FORM", "FAMILIAL PERIODIC PARALYSIS <HYPOKALEMIC FORM>", "familial periodic paralysis (& [hypokalaemic])", "Hypokalemic periodic paralysis syndrome, primary", "Familial hypokalemic periodic paralysis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypokalemic periodic paralysis", "shortest_name_length": 4}
{"curie": "MONDO:0001579", "names": ["staphyloma; cornea", "Corneal staphyloma", "cornea; staphyloma", "corneal staphyloma", "Staphyloma of cornea", "Corneal staphyloma (disorder)", "corneal staphyloma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal staphyloma", "shortest_name_length": 18}
{"curie": "MONDO:0002796", "names": ["MMBL", "Melanotic Medulloblastoma", "Melanotic medulloblastoma", "melanotic medulloblastoma", "Medulloblastoma, melanotic", "medulloblastoma, melanotic", "melanocytic medulloblastoma", "Melanocytic Medulloblastoma", "Melanocytic Medulloblastomas", "Medulloblastoma, Melanocytic", "Medulloblastomas, Melanocytic", "Medulloblastoma with Melanotic Differentiation", "medulloblastoma with melanotic differentiation", "Medulloblastoma, melanotic (morphologic abnormality)", "medulloblastoma, melanotic (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melanotic medulloblastoma", "shortest_name_length": 4}
{"curie": "UMLS:C1335341", "names": ["Paranasal Sinus Non-Hodgkin Lymphoma", "Paranasal Sinus Non-Hodgkin's Lymphoma", "Accessory Sinus Non-Hodgkin's Lymphoma", "Non-Hodgkin's Lymphoma of Paranasal Sinus", "Non-Hodgkin's Lymphoma of Accessory Sinus", "non-Hodgkin's lymphoma of accessory sinus", "Non-Hodgkin's Lymphoma of the Paranasal Sinus", "Non-Hodgkin's Lymphoma of the Accessory Sinus", "Primary Paranasal Sinus Non-Hodgkin's Lymphoma", "non-Hodgkin's lymphoma of accessory sinus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-Hodgkin's lymphoma of accessory sinus", "shortest_name_length": 36}
{"curie": "MONDO:0005903", "names": ["Pericarditis tuberculous", "Tuberculous pericarditis", "TUBERCULOUS PERICARDITIS", "pericardial tuberculosis", "Tuberculous Pericarditis", "tuberculous pericarditis", "PERICARDITIS, TUBERCULOUS", "Pericarditis, Tuberculous", "Tuberculous Pericarditides", "Tuberculosis of pericardium", "tuberculosis of pericardium", "Pericarditides, Tuberculous", "pericardium; tuberculous (etiology)", "tuberculous pericarditis (diagnosis)", "tuberculosis; pericardium (etiology)", "Tuberculosis of pericardium (disorder)", "tuberculosis of pericardium (diagnosis)", "pericardium; tuberculous (manifestation)", "tuberculosis; pericardium (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pericardial tuberculosis", "shortest_name_length": 24}
{"curie": "MONDO:0017298", "names": ["AZOOR", "Acute local occult outer retinopathy", "acute zonal occult outer retinopathy", "Acute zonal occult outer retinopathy", "Acute annular occult outer retinopathy", "AZOOR - Acute zonal occult outer retinopathy", "AAOOR - Acute annular occult outer retinopathy", "Acute zonal occult outer retinopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute zonal occult outer retinopathy", "shortest_name_length": 5}
{"curie": "UMLS:C4521879", "names": ["Stage IV", "Stage IV Pancreatic Cancer", "Stage IV Pancreatic Cancer AJCC v8", "Stage IV Exocrine Pancreatic Cancer AJCC v8", "Stage IV Exocrine Pancreatic Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Pancreatic Cancer AJCC v8", "shortest_name_length": 8}
{"curie": "MONDO:0008502", "names": ["sulfhemoglobinemia, congenital", "Sulfhemoglobinemia, Congenital", "SULFHEMOGLOBINEMIA, CONGENITAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sulfhemoglobinemia, congenital", "shortest_name_length": 30}
{"curie": "UMLS:C3495566", "names": ["reflux nephropathy", "Reflux Nephropathy", "Reflux nephropathy", "RETROGRADE NEPHROPATHY", "Reflux nephropathy (disorder)", "vesicoureteral reflux with nephropathy", "Nephropathy associated with vesicoureteral reflux", "vesicoureteral reflux with nephropathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reflux nephropathy (disorder)", "shortest_name_length": 18}
{"curie": "MONDO:0015477", "names": ["pinnae fistula or cyst"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pinnae fistula or cyst", "shortest_name_length": 22}
{"curie": "UMLS:C4525040", "names": ["Appendix Carcinoma by AJCC v8 Stage", "Appendiceal Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Appendix Carcinoma by AJCC v8 Stage", "shortest_name_length": 35}
{"curie": "MONDO:0032601", "names": ["IBDIMDE", "INFLAMMATORY BOWEL DISEASE, IMMUNODEFICIENCY, AND ENCEPHALOPATHY", "inflammatory bowel disease, immunodeficiency, and encephalopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory bowel disease, immunodeficiency, and encephalopathy", "shortest_name_length": 7}
{"curie": "MONDO:0009890", "names": ["GIKANIS", "GILLESSEN-KAESBACH-NISHIMURA SYNDROME", "Gillessen-Kaesbach-Nishimura syndrome", "polycystic kidney disease, Potter type I, with microbrachycephaly, hypertelorism, and brachymelia", "Polycystic Kidney Disease, Potter Type I, with Microbrachycephaly, Hypertelorism, and Brachymelia", "POLYCYSTIC KIDNEY DISEASE, AUTOSOMAL RECESSIVE, WITH MICROBRACHYCEPHALY, HYPERTELORISM, AND BRACHYMELIA", "polycystic kidney disease, autosomal recessive, with microbrachycephaly, hypertelorism, and brachymelia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gillessen-Kaesbach-Nishimura syndrome", "shortest_name_length": 7}
{"curie": "MONDO:0003359", "names": ["myxoid leiomyosarcoma", "Myxoid Leiomyosarcoma", "Myxoid leiomyosarcoma", "Leiomyosarcoma, Myxoid", "Myxoid Leiomyosarcomas", "Leiomyosarcomas, Myxoid", "[M] Myxoid leiomyosarcoma", "myxoid leiomyosarcoma (diagnosis)", "Myxoid leiomyosarcoma (morphologic abnormality)", "myxoid leiomyosarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myxoid leiomyosarcoma", "shortest_name_length": 21}
{"curie": "MONDO:0035105", "names": ["diaphragmatic hernia-short bowel-asplenia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diaphragmatic hernia-short bowel-asplenia syndrome", "shortest_name_length": 50}
{"curie": "MONDO:0100476", "names": ["APLD", "APLD, susceptibility to", "APLD, SUSCEPTIBILITY TO", "barraquer-simons syndrome", "BARRAQUER-SIMONS SYNDROME", "LIPODYSTROPHY, PARTIAL, PROGRESSIVE", "lipodystrophy, partial, progressive", "LIPODYSTROPHY, CEPHALOTHORACIC TYPE", "lipodystrophy, cephalothoracic type", "lipodystrophy, partial, acquired, susceptibility", "lipodystrophy, partial, acquired, susceptibility to", "LIPODYSTROPHY, PARTIAL, ACQUIRED, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lipodystrophy, partial, acquired, susceptibility to", "shortest_name_length": 4}
{"curie": "UMLS:C5670725", "names": ["Aggressive Systemic Mastocytosis Associated with Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aggressive Systemic Mastocytosis Associated with Germ Cell Tumor", "shortest_name_length": 64}
{"curie": "UMLS:C4683634", "names": ["Nodular Sclerosis Classic Hodgkin Lymphoma by Ann Arbor Stage", "Nodular Sclerosis Classical Hodgkin Lymphoma by Ann Arbor Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nodular Sclerosis Classic Hodgkin Lymphoma by Ann Arbor Stage", "shortest_name_length": 61}
{"curie": "UMLS:C0751777", "names": ["Progressive familial myoclonic epilepsy", "progressive familial myoclonic epilepsy", "Familial Progressive Myoclonic Epilepsy", "EPILEPSY, MYOCLONIC PROGRESSIVE FAMILIAL", "myoclonic; epileptic, progressive (familial)", "progressive familial myoclonic epilepsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Familial Progressive Myoclonic Epilepsy", "shortest_name_length": 39}
{"curie": "UMLS:C0158458", "names": ["Hallux;valgus", "Hallux valgus", "hallux valgus", "valgus; hallux", "hallux; valgus", "HV - Hallux valgus", "hallux abductovalgus", "Hallux abductovalgus", "Acquired hallux valgus", "Acquired Hallux Valgus", "acquired hallux valgus", "Hallux valgus (acquired)", "Hallux valgus - acquired", "HAV - Hallux abductovalgus", "Acquired hallux valgus (disorder)", "acquired hallux valgus (diagnosis)", "Hallux valgus (acquired), unspecified foot"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired hallux valgus", "shortest_name_length": 13}
{"curie": "UMLS:C1699327", "names": ["Large intestinal anastomotic leak", "Large Intestinal Anastomotic Leakage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Large Intestinal Anastomotic Leakage", "shortest_name_length": 33}
{"curie": "MONDO:0002648", "names": ["Paget; breast", "breast; Paget", "Paget's disease", "Paget cell neoplasm", "breast Paget disease", "disease nipple paget", "breast paget disease", "Breast Paget Disease", "breast disease paget", "paget disease breast", "mammary paget disease", "PAGET DISEASE MAMMARY", "Mammary Paget Disease", "disease nipples paget", "breast diseases paget", "breast pagets disease", "breast disease pagets", "pagets disease breast", "Paget Disease, Breast", "pagets breast disease", "mammary Paget disease", "disease nipple pagets", "PAGET DISEASE, BREAST", "paget's disease breast", "Paget Disease, Mammary", "Mammary Pagets Disease", "breast diseases pagets", "Pagets Disease, Breast", "breast paget's disease", "Disease, Mammary Paget", "breast disease paget's", "paget's breast disease", "Paget disease, mammary", "Mammary Paget's Disease", "Pagets Disease, Mammary", "disease nipples paget's", "mammary Paget's disease", "paget's disease mammary", "Paget Disease of Breast", "Paget disease of breast", "breast; disorder, Paget", "mammary paget's disease", "paget disease of breast", "Mammary Paget's disease", "Paget's disease, mammary", "Paget's Disease, Mammary", "Disease, Mammary Paget's", "Paget's disease (mammary)", "paget's disease of nipple", "Paget's disease of breast", "Paget's Disease of Breast", "paget's disease of breast", "Paget disease of the breast", "Paget Disease of the Breast", "Paget's Disease of the Nipple", "Paget's Disease of the Breast", "Paget's disease of the breast", "paget's disease of the breast", "paget's disease of the nipple", "Pigmented Mammary Paget Disease", "Paget's disease of breast (diagnosis)", "Paget's Disease of the Nipple and Areola", "Paget's disease, mammary (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mammary Paget disease", "shortest_name_length": 13}
{"curie": "MONDO:0013548", "names": ["ACAT2", "ACAT2D", "ACAT2 DEFICIENCY", "Acat2 deficiency", "Acat2 Deficiency", "ACAT2 deficiency, Isolated cases", "Acetocoenzyme A acetyltransferase 2", "acetoacetyl CoA thiolase, cytosolic", "Acetyl-coa acetyltransferase 2 deficiency", "ACETYL-CoA ACETYLTRANSFERASE-2 DEFICIENCY", "Acetyl CoA acetyltransferase 2 deficiency", "ACETYL-CoA acetyltransferase-2 deficiency", "acetyl-CoA acetyltransferase-2 deficiency", "Cytosolic acetoacetyl-CoA thiolase deficiency", "Acetocoenzyme A acetyltransferase 2 deficiency", "Cytosolic acetoacetyl-coenzyme A thiolase deficiency", "Cytosolic acetoacetyl-coenzyme A thiolase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acetyl-CoA acetyltransferase-2 deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0031010", "names": ["ODCD2", "ODONTOCHONDRODYSPLASIA 2 WITH HEARING LOSS AND DIABETES", "odontochondrodysplasia 2 with hearing loss and diabetes", "ondontochondrodysplasia 2 with hearing loss and diabetes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "odontochondrodysplasia 2 with hearing loss and diabetes", "shortest_name_length": 5}
{"curie": "MONDO:0010787", "names": ["KSS", "OCS syndrome", "Kearns-Sayre", "Kearn Syndrome", "kearns syndrome", "Kearns Syndrome", "Kearns' Syndrome", "Syndrome, Kearns", "Syndrome, Kearns'", "CPEO with Myopathy", "CPEO with myopathy", "CPEO WITH MYOPATHY", "Myopathy, CPEO with", "CPEO with Myopathies", "kearn sayre syndrome", "kearn sayer syndrome", "Myopathies, CPEO with", "kearn sayers syndrome", "KEARNS-SAYRE SYNDROME", "Kearns-Sayre Syndrome", "Kearns-Sayre syndrome", "kearns-sayre syndrome", "Kearns Sayre Syndrome", "kearns-sayer syndrome", "kearns sayer syndrome", "kearns sayre syndrome", "Syndrome, Kearns Sayre", "kearns sayers syndrome", "Sayre Syndrome, Kearns", "Syndrome, Kearns-Sayre", "mitochondrial Cytopathy", "CPEO with ragged red fibers", "oculocraniosomatic syndrome", "CPEO WITH RAGGED-RED FIBERS", "CPEO with ragged-Red fibers", "Oculocraniosomatic syndrome", "KSS - Kearns-Sayre syndrome", "OCULOCRANIOSOMATIC SYNDROME", "CPEO with Ragged Red Fibers", "Oculocraniosomatic Syndrome", "Cpeo With Ragged-Red Fibers", "Syndrome, Oculocraniosomatic", "Oculocraniosomatic Syndromes", "Oculocraniosomatic dystrophy", "Ophthalmoplegia-plus syndrome", "OPHTHALMOPLEGIA-PLUS SYNDROME", "Ophthalmoplegia Plus Syndrome", "ophthalmoplegia plus syndrome", "Mitochondrial ocular myopathy", "ophthalmoplegia-plus syndrome", "Ophthalmoplegia plus syndrome", "Ophthalmoplegia-Plus Syndrome", "Ophthalmoplegia Plus Syndromes", "Ophthalmoplegia-Plus Syndromes", "Syndrome, Ophthalmoplegia-Plus", "Syndrome, Ophthalmoplegia Plus", "Syndromes, Ophthalmoplegia-Plus", "Kearns-Sayre-Shy-Daroff Syndrome", "Kearns-Sayre syndrome (disorder)", "Kearns Sayre Shy Daroff Syndrome", "Kearns-Sayre syndrome (diagnosis)", "Syndrome, Kearns-Sayre-Shy-Daroff", "Kearn Sayre Mitochondrial Cytopathy", "Kearn-Sayre Mitochondrial Cytopathy", "Kearns-Sayre Mitochondrial Cytopathy", "Mitochondrial Cytopathy, Kearn-Sayre", "Cytopathy, Kearn-Sayre Mitochondrial", "Kearns-Sayre mitochondrial cytopathy", "Kearns Sayre Mitochondrial Cytopathy", "Mitochondrial Cytopathy, Kearns-Sayre", "Cytopathy, Kearns-Sayre Mitochondrial", "Kearns-Sayre Mitochondrial Cytopathies", "Cytopathies, Kearns-Sayre Mitochondrial", "Mitochondrial Cytopathies, Kearns-Sayre", "Ophthalmoplegia plus syndrome (disorder)", "Progressive external ophthalmoplegia-plus syndrome", "CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MYOPATHY", "chronic progressive external ophthalmoplegia with myopathy", "Chronic Progressive External Ophthalmoplegia with Myopathy", "ophthalmoplegia, progressive external, with ragged-Red fibers", "OPHTHALMOPLEGIA, PROGRESSIVE EXTERNAL, WITH RAGGED-RED FIBERS", "Ophthalmoplegia, Progressive External, With Ragged-Red Fibers", "ophthalmoplegia, progressive external, with ragged red fibers", "Pigmentary degeneration of the retina plus heart block syndrome", "ophthalmoplegia, pigmentary Degeneration of retina, and cardiomyopathy", "OPHTHALMOPLEGIA, PIGMENTARY DEGENERATION OF RETINA, AND CARDIOMYOPATHY", "Ophthalmoplegia, Pigmentary Degeneration of Retina, and Cardiomyopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kearns-Sayre syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C5420300", "names": ["Unresectable Testicular Epithelioid Mesothelioma", "Unresectable Paratesticular Epithelioid Mesothelioma", "Unresectable Tunica Vaginalis Epithelioid Mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Paratesticular Epithelioid Mesothelioma", "shortest_name_length": 48}
{"curie": "MONDO:0015228", "names": ["poly-X", "penta-X", "pentasomy X", "xxxxx syndrome", "XXXXX Syndrome", "XXXXX syndrome", "Five X syndrome", "XXXXX; syndrome", "syndrome; XXXXX", "Penta X syndrome", "Penta-X syndrome", "penta-X syndrome", "penta x syndrome", "Penta X Syndrome", "Pentasomy type X", "penta X syndrome", "penta X; syndrome", "49 xxxxx syndrome", "49,XXXXX syndrome", "syndrome; penta X", "49, XXXXX syndrome", "49, XXXXX Syndrome", "quintuple-X syndrome", "Pentasomy X syndrome", "pentasomy X syndrome", "chromosome X pentasomy", "XXXXX syndrome; female", "XXXXX syndrome, female", "Penta X syndrome, female", "chromosome XXXXX syndrome", "Chromosome XXXXX syndrome", "Penta X syndrome (disorder)", "syndrome; XXXXX, female, 49,XXXXX"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pentasomy X", "shortest_name_length": 6}
{"curie": "UMLS:C3873535", "names": ["Metastatic embryonal rhabdomyosarcoma", "Metastatic Embryonal Rhabdomyosarcoma", "Metastatic embryonal rhabdomyosarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic embryonal rhabdomyosarcoma", "shortest_name_length": 37}
{"curie": "MONDO:0016693", "names": ["SEGA", "subependymal giant cell astrocytoma", "Subependymal Giant Cell Astrocytoma", "Subependymal giant cell astrocytoma", "Subependymal giant-cell astrocytoma", "Astrocytoma, Subependymal Giant Cell", "[M]Subependymal giant cell astrocytoma", "Subependymal Giant Cell Astrocytic Tumor", "subependymal giant cell astrocytic tumor", "SEGA - Subependymal giant cell astrocytoma", "Subependymal Giant Cell Astrocytic Neoplasm", "subependymal giant cell astrocytic neoplasm", "Subependymal giant cell astrocytoma (disorder)", "subependymal giant cell astrocytoma (diagnosis)", "subependymal giant cell astrocytoma (morphologic abnormality)", "Subependymal giant cell astrocytoma (morphologic abnormality)", "CNS mass lesions ventricle subependymal giant cell astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subependymal giant cell astrocytoma", "shortest_name_length": 4}
{"curie": "UMLS:C1302355", "names": ["Reactive gastropathy", "Reactive gastropathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reactive gastropathy", "shortest_name_length": 20}
{"curie": "MONDO:0017562", "names": ["congenital patella dislocation, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital patella dislocation, unilateral", "shortest_name_length": 42}
{"curie": "UMLS:C4511668", "names": ["PGD", "PCBD", "Traumatic Grief", "Pathological Grief", "prolonged grief disorder", "Prolonged grief disorder", "Prolonged Grief Disorder", "Prolonged Grief Disorders", "Grief Disorder, Prolonged", "Disorder, Prolonged Grief", "Prolonged grief disorder (finding)", "prolonged grief disorder (diagnosis)", "Persistent Complex Bereavement Disorder", "Persistent complex bereavement disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prolonged grief disorder", "shortest_name_length": 3}
{"curie": "MONDO:0100028", "names": ["immune epilepsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immune epilepsy", "shortest_name_length": 15}
{"curie": "MONDO:0010763", "names": ["SPGFY1", "hypospermatogenesis", "Y-linked spermatogenic failure 1", "type I Sertoli cell-only syndrome", "Sertoli Cell-Only Syndrome, Type I", "SPERMATOGENIC FAILURE, Y-LINKED, 1", "SERTOLI CELL-ONLY SYNDROME, TYPE I", "Sertoli cell-only syndrome, type 1", "Sertoli cell-only syndrome, type 2", "spermatogenic failure, Y-linked, 1", "Y-linked Sertoli cell-only syndrome", "SERTOLI CELL-ONLY SYNDROME, TYPE II", "Sertoli Cell-Only Syndrome, Type II", "Sertoli cell-only syndrome, Y-linked", "SERTOLI CELL-ONLY SYNDROME, Y-LINKED", "INCOMPLETE SERTOLI CELL-ONLY SYNDROME", "incomplete Sertoli cell-only syndrome", "Incomplete Sertoli Cell-Only Syndrome", "spermatogenic failure, Y-linked, type 1", "spermatogenic failure, Y-linked, 1, Y-linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure, Y-linked, 1", "shortest_name_length": 6}
{"curie": "UMLS:C2987252", "names": ["Esophageal Carcinosarcoma", "Esophageal Polypoid Carcinoma", "Esophageal Spindle Cell Cancer", "Esophageal Metaplastic Carcinoma", "Esophageal Sarcomatoid Carcinoma", "Esophageal Spindle Cell Carcinoma", "Esophageal Carcinoma with Mesenchymal Stroma", "Esophageal Pseudosarcomatous Squamous Cell Carcinoma", "Esophageal Squamous Cell Carcinoma with a Spindle-Cell Component"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Spindle Cell Carcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0004173", "names": ["Skene gland carcinoma", "Carcinoma of Skene Gland", "carcinoma of Skene gland", "Carcinoma of Skene Glands", "Carcinoma of Skene's Gland", "carcinoma of Skene's gland", "paraurethral gland carcinoma", "Adenocarcinoma of Skene Gland", "adenocarcinoma of Skene gland", "carcinoma of paraurethral gland", "paraurethral gland adenocarcinoma", "Accessory Urethral Gland Carcinoma", "carcinoma of the paraurethral gland", "Adenocarcinoma of Skene Gland Origin", "adenocarcinoma of Skene gland origin", "adenocarcinoma of skene gland origin", "Accessory Urethral Gland Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenocarcinoma of skene gland origin", "shortest_name_length": 21}
{"curie": "UMLS:C1336386", "names": ["Stage IVB Oropharynx Carcinoma", "Stage IVB Carcinoma of Oropharynx", "Stage IVB Oropharyngeal Carcinoma", "Stage IVB Oropharyngeal Throat Cancer", "Stage IVB Carcinoma of the Oropharynx", "Stage IVB Oropharyngeal Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Oropharyngeal Carcinoma AJCC v7", "shortest_name_length": 30}
{"curie": "UMLS:C4551543", "names": ["Stage I", "Stage I Cancer of Testis", "stage I testicular cancer", "Stage I Testicular Cancer", "Stage I Cancer of the Testis", "Stage I Testicular Cancer AJCC v6", "Stage I Testicular Cancer AJCC v7", "Stage I Testicular Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Testicular Cancer AJCC v6 and v7", "shortest_name_length": 7}
{"curie": "MONDO:0015071", "names": ["middle ear NET", "Middle ear neuroendocrine tumor", "middle ear neuroendocrine tumor", "middle ear neuroendocrine neoplasm", "Neuroendocrine tumor of middle ear", "neuroendocrine tumor of middle ear", "Neuroendocrine tumour of middle ear", "neuroendocrine neoplasm of middle ear", "Neuroendocrine tumor of middle ear (disorder)", "middle ear neuroendocrine tumor, well differentiated, low or intermediate grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "middle ear neuroendocrine tumor", "shortest_name_length": 14}
{"curie": "MONDO:0030679", "names": ["NS14", "NOONAN SYNDROME 14", "Noonan syndrome 14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Noonan syndrome 14", "shortest_name_length": 4}
{"curie": "MONDO:0007075", "names": ["Congenital alacrima", "Alacrimia Congenita", "alacrimia congenita", "alacrima, congenital", "Alacrima, Congenital", "ALACRIMIA CONGENITA, AUTOSOMAL DOMINANT", "alacrimia congenita, autosomal dominant", "ALACRIMA, CONGENITAL, AUTOSOMAL DOMINANT", "alacrima, congenital, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alacrima, congenital, autosomal dominant", "shortest_name_length": 19}
{"curie": "UMLS:C0278737", "names": ["Stage III Lymphoblastic Lymphoma", "NHL, lymphoblastic stage III childhood", "Pediatric Lymphoblastic Lymphoma Stage III", "stage III childhood lymphoblastic lymphoma", "stage III lymphoblastic childhood lymphoma", "Stage III Childhood Lymphoblastic Lymphoma", "Stage III Pediatric Lymphoblastic Lymphoma", "Childhood Lymphoblastic Lymphoma Stage III", "Ann Arbor Stage III Childhood Lymphoblastic Lymphoma", "Stage III Childhood Precursor Lymphoblastic Lymphoma", "childhood non-Hodgkin's lymphoma, lymphoblastic stage III", "non-Hodgkin's lymphoma, lymphoblastic stage III childhood", "lymphoblastic stage III non-Hodgkin's lymphoma, childhood", "pediatric lymphoblastic non-Hodgkin's lymphoma, stage III", "lymphoma, non-Hodgkin's, lymphoblastic stage III childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Childhood Lymphoblastic Lymphoma", "shortest_name_length": 32}
{"curie": "UMLS:C4054377", "names": ["Nephrotic Syndrome - MEFV Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - MEFV Associated", "shortest_name_length": 36}
{"curie": "MONDO:0024655", "names": ["Rheumatic pericarditis", "rheumatic pericarditis", "Pericarditis rheumatic", "pericarditis; rheumatic", "Rheumatoid pericarditis", "rheumatic; pericarditis", "PERICARDITIS RHEUMATOID", "Rheumatic pericarditis, NOS", "rheumatic fever; pericarditis", "pericarditis; rheumatic fever", "Rheumatic fever with pericarditis", "rheumatic pericarditis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rheumatic pericarditis", "shortest_name_length": 22}
{"curie": "MONDO:0002466", "names": ["eye carcinoma", "Carcinoma;eye", "carcinoma eye", "Eye Carcinoma", "Carcinoma of Eye", "Ocular carcinoma", "ocular carcinoma", "carcinoma of eye", "Ocular Carcinoma", "carcinoma of the eye", "Carcinoma of the Eye", "carcinoma of eye (diagnosis)", "eyeball of camera-type eye carcinoma", "carcinoma of eyeball of camera-type eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eye carcinoma", "shortest_name_length": 13}
{"curie": "UMLS:C0220645", "names": ["pediatric st", "pediatric STS", "childhood STS", "STS, childhood", "Soft Tissue Sarcoma", "Soft tissue sarcoma, child", "Pediatric Soft Tissue Sarcoma", "Childhood Soft Tissue Sarcoma", "pediatric soft tissue sarcoma", "childhood sarcoma soft tissue", "childhood soft tissue sarcoma", "soft tissue sarcoma, childhood", "Pediatric Sarcoma of Soft Tissue", "Childhood Sarcoma of Soft Tissue", "Childhood Sarcoma of the Soft Tissue", "Pediatric Sarcoma of the Soft Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Soft Tissue Sarcoma", "shortest_name_length": 12}
{"curie": "UMLS:C0920506", "names": ["Environmental Cancer", "Environmental Cancers", "Environment-Related Cancer", "environment related cancer", "Environmental Malignant Neoplasm", "Environment-Related Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Environment-Related Malignant Neoplasm", "shortest_name_length": 20}
{"curie": "MONDO:0007306", "names": ["KFS", "Kfs", "KFS1", "Klippel-Feil syndrome 1", "GDF6 isolated Klippel-Feil syndrome", "Klippel Feil syndrome dominant type", "Klippel-Feil syndrome, autosomal dominant", "KLIPPEL-FEIL SYNDROME, AUTOSOMAL DOMINANT", "KLIPPEL-FEIL SYNDROME 1, AUTOSOMAL DOMINANT", "Klippel-FEIL syndrome 1, autosomal dominant", "Klippel-Feil syndrome 1, autosomal dominant", "cervical vertebral fusion, autosomal dominant", "CERVICAL VERTEBRAL FUSION, AUTOSOMAL DOMINANT", "Cervical vertebral fusion, autosomal dominant", "isolated Klippel-Feil syndrome caused by mutation in GDF6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Klippel-Feil syndrome 1, autosomal dominant", "shortest_name_length": 3}
{"curie": "UMLS:C3640020", "names": ["D-Transposition of the Great Vessels with Ventricular Septal Defect", "Dextro-Transposition of the Great Vessels with Ventricular Septal Defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dextro-Transposition of the Great Vessels with Ventricular Septal Defect", "shortest_name_length": 67}
{"curie": "MONDO:0000233", "names": ["Japanese spotted fever", "Japanese Spotted Fever", "oriental spotted fever", "Spotted Fever, Japanese", "spotted fever, Japanese", "Fever, Japanese Spotted", "Japanese Spotted Fevers", "Japanese spotted fevers", "fever, Japanese spotted", "Fevers, Japanese Spotted", "fevers, Japanese spotted", "Rickettsia japonica spotted fever", "Japanese spotted fever (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Japanese spotted fever", "shortest_name_length": 22}
{"curie": "UMLS:C4288774", "names": ["Uterine Corpus Malignant PEComa", "Malignant Uterine Corpus PEComa", "Uterine Corpus Malignant Perivascular Epithelioid Cell Tumor", "Malignant Uterine Corpus Perivascular Epithelioid Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Corpus Malignant PEComa", "shortest_name_length": 31}
{"curie": "MONDO:0021067", "names": ["Thymic Germ Cell Tumor", "thymic germ cell tumor", "Mediastinal Germ Cell Tumor", "mediastinal germ cell tumor", "mediastinum germ cell tumor", "Mediastinal Germ Cell Neoplasm", "Germ Cell Tumor of Mediastinum", "germ cell tumor of mediastinum", "mediastinal germ cell neoplasm", "germ cell neoplasm of mediastinum", "Germ Cell Neoplasm of Mediastinum", "Germ Cell Tumor of the Mediastinum", "germ cell tumor of the mediastinum", "germ cell neoplasm of the mediastinum", "Germ Cell Neoplasm of the Mediastinum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mediastinal germ cell tumor", "shortest_name_length": 22}
{"curie": "MONDO:0100396", "names": ["AML, t(7;12)(q36;p13)", "AML with t(7;12)(q36;p13); MNX1-ETV6", "AML with t(7;12)(q36;p13); HLXB9-ETV6", "acute myeloid leukemia, t(7;12)(q36;p13)", "Acute Myeloid Leukemia with t(7;12)(q36;p13); MNX1-ETV6", "Acute Myeloid Leukemia with t(7;12)(q36;p13); HLXB9-ETV6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, t(7;12)(q36;p13)", "shortest_name_length": 21}
{"curie": "MONDO:0003551", "names": ["thymus adenosquamous carcinoma", "thymic adenosquamous carcinoma", "Thymus Adenosquamous Carcinoma", "Thymus adenosquamous carcinoma", "Thymic Adenosquamous Carcinoma", "Adenosquamous Carcinoma of Thymus", "adenosquamous carcinoma of Thymus", "Adenosquamous Carcinoma of the Thymus", "Adenosquamous carcinoma of the Thymus", "adenosquamous carcinoma of the Thymus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thymic adenosquamous carcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0002762", "names": ["esophageal verrucous cancer", "Esophageal Verrucous Cancer", "esophagus verrucous carcinoma", "Esophageal Verrucous Carcinoma", "oesophagus verrucous carcinoma", "esophageal verrucous carcinoma", "verrucous carcinoma of esophagus", "Verrucous Carcinoma of Esophagus", "verrucous carcinoma of oesophagus", "verrucous carcinoma of the esophagus", "Verrucous Carcinoma of the Esophagus", "verrucous carcinoma of esophagus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophagus verrucous carcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C5418784", "names": ["Upper Alveolar Ridge Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Upper Alveolar Ridge Squamous Cell Carcinoma", "shortest_name_length": 44}
{"curie": "MONDO:0021851", "names": ["Alopecia universalis onychodystrophy vitiligo", "alopecia universalis onychodystrophy vitiligo", "Alopecia universalis, onychodystrophy, and total vitiligo", "alopecia universalis, onychodystrophy, and total vitiligo"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alopecia universalis onychodystrophy vitiligo", "shortest_name_length": 45}
{"curie": "UMLS:C1698481", "names": ["Upper aerodigestive tract infection", "Upper Aerodigestive Tract Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Upper aerodigestive tract infection", "shortest_name_length": 35}
{"curie": "UMLS:C1336717", "names": ["testicular teratoma with seminoma and embryonal carcinoma", "testicular embryonal carcinoma and teratoma with seminoma", "embryonal carcinoma and teratoma with seminoma, testicular", "teratoma with seminoma and embryonal carcinoma of the testis", "testis cancer, embryonal carcinoma and teratoma with seminoma", "testis cancer, teratoma with seminoma and embryonal carcinoma", "Mixed Embryonal Carcinoma and Teratoma with Seminoma of Testis", "Testicular Mixed Embryonal Carcinoma and Teratoma with Seminoma", "testicle cancer, embryonal carcinoma and teratoma with seminoma", "testicular cancer, teratoma with seminoma and embryonal carcinoma", "testicular cancer, embryonal carcinoma and teratoma with seminoma", "Mixed Embryonal Carcinoma and Teratoma with Seminoma of the Testis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular Mixed Embryonal Carcinoma and Teratoma with Seminoma", "shortest_name_length": 57}
{"curie": "UMLS:C4520895", "names": ["Stage 0 Large Cell Lung Cancer", "Stage 0 Large Cell Carcinoma of Lung", "Stage 0 Large Cell Carcinoma of the Lung", "Stage 0 Large Cell Lung Carcinoma AJCC v6", "Stage 0 Large Cell Lung Carcinoma AJCC v7", "Stage 0 Lung Large Cell Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Lung Large Cell Carcinoma AJCC v6 and v7", "shortest_name_length": 30}
{"curie": "MONDO:0000521", "names": ["salivary carcinoma", "salivary gland cancer", "Salivary Gland Cancer", "Salivary Gland Carcinoma", "Salivary gland carcinoma", "salivary gland carcinoma", "carcinoma gland salivary", "carcinoma glands salivary", "Carcinoma of Salivary Gland", "carcinoma of salivary gland", "Carcinoma of the Salivary Gland", "carcinoma of the salivary gland", "saliva-secreting gland carcinoma", "carcinoma of saliva-secreting gland", "carcinoma of salivary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "salivary gland carcinoma", "shortest_name_length": 18}
{"curie": "MONDO:0008896", "names": ["Cumming syndrome", "CUMMING SYNDROME", "campomelia Cumming type", "Campomelia Cumming type", "CAMPOMELIA, CUMMING TYPE", "Campomelia, Cumming Type", "Campomelia, Cumming type", "campomelia, Cumming type", "Campomelia Cumming type (disorder)", "CERVICAL LYMPHOCELE WITH BOWED LONG BONES", "cervical lymphocele with bowed long bones", "Cervical lymphocele with bowed long bones", "campomelia, cervical lymphocele, polysplenia, and multicystic dysplastic kidneys"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "campomelia, Cumming type", "shortest_name_length": 16}
{"curie": "UMLS:C1335052", "names": ["Non-Neoplastic Uveal Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Uveal Disorder", "shortest_name_length": 29}
{"curie": "MONDO:0033821", "names": ["keratomycosis", "Keratomycosis", "Keratitis fungal", "Fungal Keratitis", "Fungal keratitis", "fungal keratitis", "mycotic keratitis", "keratitis mycotic", "Mycotic keratitis", "Fungal infection of cornea", "Fungal keratitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fungal keratitis", "shortest_name_length": 13}
{"curie": "UMLS:C1514517", "names": ["STUMP", "Prostate Stromal Tumor of Uncertain Malignant Potential", "Prostate Stromal Proliferation of Uncertain Malignant Potential"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Stromal Proliferation of Uncertain Malignant Potential", "shortest_name_length": 5}
{"curie": "MONDO:0003781", "names": ["chest cold", "bronchitis", "Bronchitis", "BRONCHITIS", "Bronchitides", "Bronchitis NOS", "Chest infection", "chest infection", "Bronchitis, NOS", "acute bronchitis", "acute Bronchitis", "chronic bronchitis", "bronchial infection", "Bronchial infection", "CI - chest infection", "CI - Chest infection", "bronchus inflammation", "Bronchitis (disorder)", "bronchitis (diagnosis)", "Inflammation of bronchus", "inflammation of bronchus", "recurrent wheezy bronchitis", "acute bronchitis and bronchiolitis", "Bronchitis, not specified as acute or chronic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bronchitis", "shortest_name_length": 10}
{"curie": "MONDO:0006281", "names": ["Lung Signet-Ring Cell Carcinoma", "signet ring lung adenocarcinoma", "lung signet ring cell carcinoma", "Lung Signet Ring Cell Carcinoma", "signet ring cell carcinoma of lung", "Signet ring cell carcinoma of lung", "Primary signet ring cell carcinoma of lung", "Signet ring cell carcinoma of lung (disorder)", "signet ring cell carcinoma of lung (diagnosis)", "Primary signet ring cell carcinoma of lung (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung signet ring cell carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0004400", "names": ["malignant type A thymoma", "Malignant Type A Thymoma", "Thymoma, type A, malignant", "thymoma, medullary, malignant", "Thymoma, medullary, malignant", "Spindle cell malignant thymoma", "Thymoma, spindle cell, malignant", "Thymoma, type A, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant type A thymoma", "shortest_name_length": 24}
{"curie": "MONDO:0007785", "names": ["DTTRH", "euthryroidal hyperthyroxinemia 2", "EUTHRYROIDAL HYPERTHYROXINEMIA 2", "Hyperthyroxinemia, Dysprealbuminemic", "hyperthyroxinemia, Dysprealbuminemic", "HYPERTHYROXINEMIA, DYSPREALBUMINEMIC", "DYSTRANSTHYRETINEMIC HYPERTHYROXINEMIA", "dystransthyretinemic hyperthyroxinemia", "hyperthyroxinemia, dystransthyretinemic", "HYPERTHYROXINEMIA, DYSTRANSTHYRETINEMIC", "Hyperthyroxinemia, Dystransthyretinemic", "dystransthyretinemic ethyroidal hyperthyroxinemia", "DYSTRANSTHYRETINEMIC EUTHYROIDAL HYPERTHYROXINEMIA", "Dystransthyretinemic Euthyroidal Hyperthyroxinemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperthyroxinemia, dystransthyretinemic", "shortest_name_length": 5}
{"curie": "UMLS:C0853312", "names": ["Osteoarthritis aggravated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Osteoarthritis aggravated", "shortest_name_length": 25}
{"curie": "MONDO:0015486", "names": ["KC", "Keratoconus", "keratoconus", "KERATOCONUS", "conical cornea", "Cornea conical", "Bulging cornea", "Conical cornea", "cornea; conical", "conical; cornea", "Keratoconus, NOS", "isolated keratoconus", "keratoconus (disease)", "Keratoconus (disorder)", "keratoconus (diagnosis)", "Keratoconus, unspecified", "keratoconus (physical finding)", "noninflammatory corneal thining"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratoconus", "shortest_name_length": 2}
{"curie": "MONDO:0044876", "names": ["DHS", "DRESS", "dress", "DRESS Syndrome", "DRESS syndrome", "DRESS Syndromes", "Drug Hypersensitivity Syndrome", "drug hypersensitivity syndrome", "Drug hypersensitivity syndrome", "Syndrome, Drug Hypersensitivity", "Hypersensitivity Syndrome, Drug", "Drug Hypersensitivity Syndromes", "Hypersensitivity Syndromes, Drug", "Syndromes, Drug Hypersensitivity", "Drug-induced hypersensitivity syndrome", "Anticonvulsant hypersensitivity syndrome", "Drug rash with eosinophilia and systemic symptoms", "Drug Reaction With Eosinophilia And Systemic Symptom", "Drug Reaction with Eosinophilia and Systemic Symptoms", "Drug reaction with eosinophilia and systemic symptoms", "Drug reaction with eosinophilia and Systemic symptoms", "drug rash with eosinophilia and systemic symptoms syndrome", "Drug rash with eosinophilia and systemic symptoms syndrome", "Drug Reaction with Eosinophilia and Systemic Symptoms Syndrome", "Drug reaction with eosinophilia and systemic symptoms (disorder)", "drug rash with eosinophilia and systemic symptoms syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "drug hypersensitivity syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C5420536", "names": ["Advanced Cervical Adenosquamous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Cervical Adenosquamous Carcinoma", "shortest_name_length": 41}
{"curie": "OMIM:612460", "names": ["BMIQ14", "OBESITY, SUSCEPTIBILITY TO", "BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 6}
{"curie": "UMLS:C5206833", "names": ["Parapharyngeal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parapharyngeal Neoplasm", "shortest_name_length": 23}
{"curie": "MONDO:0016717", "names": ["Choroid Plexus Tumor", "Choroid plexus tumor", "choroid plexus tumor", "Choroid Plexus Tumors", "Choroid Plexus Neoplasm", "Tumor of choroid plexus", "tumor of choroid plexus", "Tumor of Choroid Plexus", "choroid plexus neoplasm", "Tumour of choroid plexus", "Neoplasm, Choroid Plexus", "Choroid Plexus Neoplasms", "Neoplasms, Choroid Plexus", "neoplasm of choroid plexus", "Neoplasm of Choroid Plexus", "Tumor of the Choroid Plexus", "tumor of the choroid plexus", "Neoplasm of the Choroid Plexus", "neoplasm of the choroid plexus", "Tumor of choroid plexus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choroid plexus neoplasm", "shortest_name_length": 20}
{"curie": "MONDO:0017266", "names": ["KPI", "keratinopathic ichthyosis", "Keratinopathic ichthyosis", "Keratinopathic ichthyosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratinopathic ichthyosis", "shortest_name_length": 3}
{"curie": "MONDO:0025417", "names": ["fowlpox", "Fowlpox", "Birdpox", "Bird pox", "Fowl Pox", "fowl pox", "Fowl pox", "pox, Bird", "pox, fowl", "Pox, Fowl", "Variola avium", "Variola Avium", "fowl diphtheria", "Fowl Diphtheria", "diphtheria, fowl", "fowl Diphtherias", "Fowl Diphtherias", "Diphtheria, Fowl", "Diphtherias, Fowl", "Diphtherias, fowl", "Fowlpox (disorder)", "epithelioma contagiosum", "Epithelioma Contagiosum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fowlpox", "shortest_name_length": 7}
{"curie": "UMLS:C0279942", "names": ["pediatric metastatic STS", "childhood metastatic STS", "childhood STS, metastatic", "pediatric STS, metastatic", "STS, metastatic, childhood", "Metastatic Soft Tissue Sarcoma", "stage IV childhoood soft tissue sarcoma", "Metastatic Childhood Soft Tissue Sarcoma", "metastatic childhood soft tissue sarcoma", "Metastatic Pediatric Soft Tissue Sarcoma", "childhood soft tissue sarcoma, metastatic", "soft tissue sarcoma, childhood, metastatic", "Metastatic Pediatric Sarcoma of Soft Tissue", "Metastatic Childhood Sarcoma of Soft Tissue", "Metastatic Pediatric Sarcoma of the Soft Tissue", "Metastatic Childhood Sarcoma of the Soft Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Childhood Soft Tissue Sarcoma", "shortest_name_length": 24}
{"curie": "MONDO:0001469", "names": ["cascade stomach", "Cascade stomach", "Hourglass stomach", "stomach; hourglass", "Cascade stomach (disorder)", "hourglass contraction; stomach, stricture", "stomach; hourglass contraction, stricture", "Hourglass stricture or stenosis of stomach", "hourglass stricture or stenosis of stomach", "Hourglass stricture and stenosis of stomach"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cascade stomach", "shortest_name_length": 15}
{"curie": "MONDO:0017940", "names": ["CMT2 due to KIF5A mutation", "autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation", "Autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation", "Autosomal dominant Charcot-Marie-Tooth disease type 2 due to kinesin family member 5A mutation", "Autosomal dominant Charcot-Marie-Tooth disease type 2 due to kinesin family member 5A mutation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation", "shortest_name_length": 26}
{"curie": "MONDO:0023129", "names": ["Fara Chlupackova syndrome", "[OBSOLETE] Fara Chlupackova syndrome", "familial oto-facio-cervical dysmorphia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fara Chlupackova syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0011399", "names": ["A-thalassemia", "A-Thalassemia", "Thalassemia alpha", "thalassemia alpha", "Alpha-thalassemia", "Alpha thalassemia", "Alpha Thalassemia", "alpha Thalassemia", "alpha thalassemia", "alpha-Thalassemia", "ALPHA-THALASSEMIA", "Thalassemia-alpha", "alpha-thalassemia", "THALASSEMIA ALPHA", "alpha-Thalassemias", "Thalassaemia alpha", "Alpha thalassaemia", "alpha; thalassemia", "Thalassemia, Alpha", "Alpha-thalassaemia", "thalassemia; alpha", "alpha thalassemias", "alpha thalassaemia", "alpha-thalassaemia", "thalassemia, alpha-", "Hemoglobin H Disease", "Hemoglobin H disease", "thalassemias, alpha-", "Disease, Hemoglobin H", "Haemoglobin H disease", "alpha Thalassemia, NOS", "Alpha thalassemia syndrome", "Alpha thalassaemia syndrome", "Alpha thalassemia (disorder)", "alpha thalassemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alpha thalassemia", "shortest_name_length": 13}
{"curie": "MONDO:0004321", "names": ["Mixed cell adenocarcinoma", "Endometrial Mixed Carcinoma", "endometrial mixed adenocarcinoma", "Endometrial Mixed Cell Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometrial mixed adenocarcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0010823", "names": ["Rcdp3", "RCDP3", "Agps Deficiency", "AGPS DEFICIENCY", "AGPS deficiency", "AGPS rhizomelic chondrodysplasia punctata", "rhizomelic chondrodysplasia punctata type 3", "Rhizomelic chondrodysplasia punctata type 3", "RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 3", "rhizomelic chondrodysplasia punctata, type 3", "alkylglycerone-phosphate synthase deficiency", "Alkylglycerone-Phosphate Synthase Deficiency", "ALKYLGLYCERONE-PHOSPHATE SYNTHASE DEFICIENCY", "Rhizomelic chondrodysplasia punctata, type 3", "Alkyldihydroxyacetonephosphate synthase deficiency", "Alkyldihydroxyacetonephosphate Synthase Deficiency", "alkyldihydroxyacetonephosphate synthase deficiency", "ALKYLDIHYDROXYACETONEPHOSPHATE SYNTHASE DEFICIENCY", "Rhizomelic chondrodysplasia punctata type 3 (disorder)", "rhizomelic chondrodysplasia punctata type 3 (diagnosis)", "rhizomelic chondrodysplasia punctata caused by mutation in AGPS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rhizomelic chondrodysplasia punctata type 3", "shortest_name_length": 5}
{"curie": "UMLS:C4527054", "names": ["Merkel Cell Carcinoma by AJCC v7 Stage", "Neuroendocrine Carcinoma of the Skin by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Merkel Cell Carcinoma by AJCC v7 Stage", "shortest_name_length": 38}
{"curie": "MONDO:0000294", "names": ["Mesocestoidosis", "Mesocestoidiasis", "mesocestoidiasis", "infection by Mesocestoides", "Infection by Mesocestoides", "Infection by Mesocestoides, NOS", "Mesocestoides infectious disease", "infection caused by Mesocestoides", "Mesocestoides disease or disorder", "Infection caused by Mesocestoides", "Infection by Mesocestoides lineatus", "Mesocestoides caused disease or disorder", "Infection caused by Mesocestoides lineatus", "Infection caused by Mesocestoides (disorder)", "Infection caused by Mesocestoides lineatus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mesocestoidiasis", "shortest_name_length": 15}
{"curie": "UMLS:C5206410", "names": ["Advanced Soft Tissue Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Soft Tissue Sarcoma", "shortest_name_length": 28}
{"curie": "MONDO:0014229", "names": ["MCOPS12", "syndromic microphthalmia-12", "syndromic microphthalmia 12", "microphthalmia, syndromic 12", "MICROPHTHALMIA, SYNDROMIC 12", "RARB syndromic microphthalmia", "microphthalmia, syndromic type 12", "syndromic microphthalmia caused by mutation in RARB", "microphthalmia with or without pulmonary hypoplasia, diaphragmatic hernia, and/or Cardiac defects", "microphthalmia with or without pulmonary hypoplasia, diaphragmatic hernia, and/or cardiac defects", "MICROPHTHALMIA WITH OR WITHOUT PULMONARY HYPOPLASIA, DIAPHRAGMATIC HERNIA, AND/OR CARDIAC DEFECTS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microphthalmia, syndromic 12", "shortest_name_length": 7}
{"curie": "MONDO:0006155", "names": ["colon NET G1", "Colon NET G1", "Colon Carcinoid Tumor", "colon carcinoid tumor", "Colonic Carcinoid Tumor", "colonic carcinoid tumor", "Carcinoid Tumor of Colon", "carcinoid tumor of colon", "Carcinoid tumor in colon", "Carcinoid tumour in colon", "Carcinoid Tumor of the Colon", "carcinoid tumor of the colon", "Colon Neuroendocrine Tumor G1", "colon neuroendocrine tumor G1", "colon carcinoid tumor (disease)", "colon neuroendocrine neoplasm G1", "grade 1 neuroendocrine neoplasm of colon", "colon neuroendocrine tumor, well differentiated, low grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colon neuroendocrine tumor G1", "shortest_name_length": 12}
{"curie": "MONDO:0019611", "names": ["TSHoma", "TSH-oma", "thyrotropinoma", "Thyrotropinoma", "thyrotrope adenoma", "Thyrotroph Adenoma", "Thyrotroph adenoma", "Thyrotrope Adenoma", "thyrotroph adenoma", "Thyrotrophic Adenoma", "thyrotrophic adenoma", "TSH secreting adenoma", "TSH-producing adenoma", "TSH-producing Adenoma", "adenoma, TSH secreting", "Thyrotroph PitNET/Adenoma", "TSH producing pituitary tumor", "Thyrotroph adenoma (disorder)", "pituitary thyrotrophic adenoma", "Pituitary thyrotrophic adenoma", "pituitary tumor, TSH producing", "TSH Secreting Pituitary Adenoma", "TSH secreting pituitary adenoma", "TSH producing pituitary adenoma", "TSH Producing Pituitary Adenoma", "TSH-secreting pituitary adenoma", "TSH Producing Adenoma of Pituitary", "TSH secreting adenoma of pituitary", "TSH Secreting Adenoma of Pituitary", "TSH producing adenoma of pituitary", "TSH-Producing Pituitary Gland Adenoma", "TSH producing pituitary gland adenoma", "TSH-producing pituitary gland adenoma", "TSH Producing Pituitary Gland Adenoma", "TSH secreting pituitary gland adenoma", "TSH Secreting Pituitary Gland Adenoma", "TSH secreting adenoma of the pituitary", "TSH producing adenoma of the pituitary", "TSH Secreting Adenoma of the Pituitary", "TSH Producing Adenoma of the Pituitary", "Thyrotropin-secreting pituitary adenoma", "TSH producing adenoma of pituitary gland", "TSH Producing Adenoma of Pituitary Gland", "TSH secreting adenoma of pituitary gland", "TSH Secreting Adenoma of Pituitary Gland", "Thyrotroph Pituitary Neuroendocrine Tumor", "TSH Secreting Adenoma of the Pituitary Gland", "TSH Producing Adenoma of the Pituitary Gland", "TSH producing adenoma of the pituitary gland", "TSH secreting adenoma of the pituitary gland", "thyroid stimulating hormone-producing adenoma", "Thyroid Stimulating Hormone-Producing Adenoma", "thyrotropin producing pituitary gland adenoma", "Thyrotropin Producing Pituitary Gland Adenoma", "Thyrotroph Pituitary Neuroendocrine Tumor/Adenoma", "Thyroid Stimulating Hormone Producing Pituitary Adenoma", "Thyroid Stimulating Hormone Secreting Pituitary Adenoma", "Thyroid stimulating hormone-secreting pituitary adenoma", "thyroid stimulating hormone-secreting pituitary adenoma", "thyroid stimulating hormone secreting pituitary adenoma", "thyroid stimulating hormone producing pituitary adenoma", "thyroid stimulating hormone secreting adenoma of pituitary", "thyroid stimulating hormone producing adenoma of pituitary", "Thyroid Stimulating Hormone Producing Adenoma of Pituitary", "Thyroid Stimulating Hormone Secreting Adenoma of Pituitary", "Thyroid Stimulating Hormone Secreting Pituitary Gland Adenoma", "Thyroid Stimulating Hormone Producing Pituitary Gland Adenoma", "thyroid stimulating hormone producing pituitary gland adenoma", "thyroid stimulating hormone secreting pituitary gland adenoma", "thyroid stimulating hormone secreting adenoma of the pituitary", "thyroid stimulating hormone producing adenoma of the pituitary", "Thyroid Stimulating Hormone Secreting Adenoma of the Pituitary", "Thyroid Stimulating Hormone Producing Adenoma of the Pituitary", "thyroid stimulating hormone secreting adenoma of pituitary gland", "thyroid stimulating hormone producing adenoma of pituitary gland", "Thyroid Stimulating Hormone Producing Adenoma of Pituitary Gland", "Thyroid Stimulating Hormone Secreting Adenoma of Pituitary Gland", "Thyroid Stimulating Hormone Secreting Adenoma of the Pituitary Gland", "Thyroid Stimulating Hormone Producing Adenoma of the Pituitary Gland", "thyroid stimulating hormone producing adenoma of the pituitary gland", "thyroid stimulating hormone secreting adenoma of the pituitary gland", "thyroid stimulating hormone producing adenoma of pituitary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "TSH-secreting pituitary adenoma", "shortest_name_length": 6}
{"curie": "MONDO:0018891", "names": ["familial tumoral calcinosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial tumoral calcinosis", "shortest_name_length": 27}
{"curie": "MONDO:0018775", "names": ["axonal HMSN", "axonal hereditary motor and sensory neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "axonal hereditary motor and sensory neuropathy", "shortest_name_length": 11}
{"curie": "UMLS:C0021367", "names": ["Mammary Ductal Carcinoma", "Mammary Ductal Carcinomas", "Carcinoma, Mammary Ductal", "Carcinomas, Mammary Ductal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mammary Ductal Carcinoma", "shortest_name_length": 24}
{"curie": "UMLS:C4524375", "names": ["Lung Adenofibroma", "Pulmonary Adenofibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Adenofibroma", "shortest_name_length": 17}
{"curie": "MONDO:0004770", "names": ["PROPTOSIS", "Proptoses", "proptosis", "Proptosis", "Bulging eye", "Eye bulging", "bulging eye", "Bulging eyes", "Exophthalmos", "EXOPHTHALMOS", "exophthalmos", "exophthalmia", "Exophthalmia", "bulging eyes", "Proptosis, NOS", "Prominent eyes", "Protruding eyes", "Protrusio bulbi", "OCULAR PROPTOSIS", "Exophthalmos NOS", "Ocular proptosis", "Prominent globes", "eyes bulging out", "Exophthalmos, NOS", "Eyeballs bulging out", "exophthalmos (disease)", "Eye displaced forwards", "Exophthalmos (disorder)", "exophthalmos (diagnosis)", "Unspecified exophthalmos", "Exophthalmos, unspecified", "eyes bulging out (symptom)", "eyes bulging out as symptom", "proptosis (physical finding)", "Anterior bulging of the globe", "Anterior bulging of the globe of eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exophthalmos", "shortest_name_length": 9}
{"curie": "MONDO:0030938", "names": ["SPGF52", "spermatogenic failure 52", "SPERMATOGENIC FAILURE 52"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 52", "shortest_name_length": 6}
{"curie": "MONDO:0001580", "names": ["lacrimal duct cancer", "Malignant Lacrimal Duct Tumor", "malignant lacrimal duct tumor", "lacrimal drainage system cancer", "malignant tumor of lacrimal duct", "Malignant Lacrimal Duct Neoplasm", "malignant lacrimal duct neoplasm", "Malignant Tumor of Lacrimal Duct", "cancer of lacrimal drainage system", "malignant neoplasm of lacrimal duct", "Malignant Neoplasm of Lacrimal Duct", "Malignant neoplasm of lacrimal duct", "malignant tumor of the lacrimal duct", "Malignant Tumor of the Lacrimal Duct", "malignant tumor of nasolacrimal duct", "Malignant Nasolacrimal Duct Neoplasm", "malignant neoplasm of the lacrimal duct", "Malignant neoplasm of nasolacrimal duct", "Malignant Neoplasm of the Lacrimal Duct", "malignant neoplasm of nasolacrimal duct", "malignant lacrimal drainage system neoplasm", "malignant neoplasm of lacrimal drainage system", "malignant neoplasm of lacrimal duct (diagnosis)", "Malignant neoplasm of nasolacrimal duct (disorder)", "malignant neoplasm of nasolacrimal duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lacrimal duct cancer", "shortest_name_length": 20}
{"curie": "MONDO:0000009", "names": ["Thrombocytopathy", "THROMBOCYTOPATHY", "thrombocytopathy", "Platelet Disorder", "DISORDER PLATELET", "platelet disorder", "Thrombocytopathia", "Platelet disorder", "PLATELET DISORDER", "disorder platelet", "platelet disorders", "Platelet Disorders", "PLATELET DISORDERS", "Thrombocytopathies", "thrombocytopathies", "Platelet disorders", "disorders platelets", "Platelet Abnormality", "thrombocyte disorders", "Thrombocytopathy, NOS", "Thrombocyte disorders", "Platelet disorder, NOS", "blood platelet disease", "blood platelet disorder", "platelet blood disorder", "Blood Platelet Disorder", "blood disorder platelet", "blood platelet disorders", "Platelet Disorder, Blood", "Blood Platelet Disorders", "Disorder, Blood Platelet", "Blood platelet disorders", "Disorders, Blood Platelet", "Platelet Disorders, Blood", "Abnormal platelets present", "thrombocytopathy (diagnosis)", "Platelet disorder (disorder)", "platelet disorders (diagnosis)", "bleeding disorder, platelet-type", "Platelet disorder, disease or syndrome", "inherited bleeding disorder, platelet-type", "Platelet Disorders, Diseases and Syndromes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited bleeding disorder, platelet-type", "shortest_name_length": 16}
{"curie": "MONDO:0020659", "names": ["UTUC", "upper tract urothelial carcinoma", "transitional cell carcinoma of the pelvis and ureter", "transitional cell carcinoma of the upper urinary tract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "upper tract urothelial carcinoma", "shortest_name_length": 4}
{"curie": "UMLS:C1334601", "names": ["Malignant Soft Tissue Tumor of Uncertain Differentiation", "Malignant Soft Tissue Neoplasm of Uncertain Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Soft Tissue Tumor of Uncertain Differentiation", "shortest_name_length": 56}
{"curie": "OMIM:612362", "names": ["BMIQ12", "OBESITY, SUSCEPTIBILITY TO", "BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 12", "BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 12 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 6}
{"curie": "MONDO:0005923", "names": ["Pneumocystis infection", "Pneumocystis Infection", "Pneumocystis infections", "Infection, Pneumocystis", "Pneumocystis Infections", "infections, Pneumocystis", "PNEUMOCYSTIS CARINII INFECTION", "Pneumocystis carinii infection", "Pneumocystis carinii; infection", "infection; Pneumocystis carinii", "Pneumocystis infectious disease", "Pneumocystis carinii Infections", "Infection by Pneumocystis carinii"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pneumocystis infectious disease", "shortest_name_length": 22}
{"curie": "MONDO:0002580", "names": ["orbit rhabdomyosarcoma", "Orbit Rhabdomyosarcoma", "rhabdomyosarcoma of orbit", "Rhabdomyosarcoma of Orbit", "Rhabdomyosarcoma of orbit", "rhabdomyosarcoma of the orbit", "Rhabdomyosarcoma of the Orbit", "Rhabdomyosarcoma of the orbit", "orbital region rhabdomyosarcoma", "Rhabdomyosarcoma of orbit (disorder)", "rhabdomyosarcoma of orbit (diagnosis)", "orbital region rhabdomyosarcoma (disease)", "orbit neoplasm malignant rhabdomyosarcoma", "rhabdomyosarcoma (disease) of orbital region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orbit rhabdomyosarcoma", "shortest_name_length": 22}
{"curie": "MONDO:0000959", "names": ["Malignant hypertensive renal disease", "malignant hypertensive renal disease", "Hypertensive renal disease, malignant", "Malignant hypertensive renal disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant hypertensive renal disease", "shortest_name_length": 36}
{"curie": "UMLS:C0496924", "names": ["Neoplasm of uncertain behavior of testis", "neoplasm of uncertain behavior of testis", "Neoplasm of uncertain behaviour of testis", "testicular neoplasm of uncertain behavior", "Neoplasm of uncertain behavior of testis, NOS", "Neoplasm of uncertain behaviour of testis, NOS", "Neoplasm of uncertain or unknown behavior of testis", "Neoplasm of uncertain behavior of testis (disorder)", "neoplasm of uncertain behavior of testis (diagnosis)", "Neoplasm of uncertain or unknown behaviour of testis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplasm of uncertain or unknown behavior of testis", "shortest_name_length": 40}
{"curie": "MONDO:0003322", "names": ["Epithelial Predominant Wilms Tumor", "epithelial predominant Wilms tumor", "epithelial predominant Wilm's tumor", "epithelial predominant Wilms' tumor", "Wilms tumor, epithelial predominant", "epithelial predominant Wilms' tumour", "Wilm's tumor, epithelial predominant", "Wilms' tumor, epithelial predominant", "Epithelial Predominant Nephroblastoma", "epithelial predominant nephroblastoma", "Epithelial Predominant Renal Wilms Tumor", "epithelial predominant renal Wilms tumor", "epithelial Predominant renal Wilms tumor", "Epithelial Predominant Kidney Wilms Tumor", "Epithelial Predominant Renal Adenosarcoma", "epithelial predominant renal adenosarcoma", "epithelial Predominant renal Wilms tumour", "epithelial predominant renal Wilm's tumor", "Epithelial Predominant Renal Wilms' Tumor", "epithelial predominant kidney Wilms tumor", "Epithelial Predominant Renal Wilm's Tumor", "epithelial predominant renal Wilms' tumor", "epithelial predominant kidney adenosarcoma", "Epithelial Predominant Kidney Adenosarcoma", "Epithelial Predominant Kidney Nephroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epithelial predominant Wilms' tumor", "shortest_name_length": 34}
{"curie": "UMLS:C4525734", "names": ["Posterior Subcapsular Cataract Grade 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Posterior Subcapsular Cataract Grade 4", "shortest_name_length": 38}
{"curie": "UMLS:C0700226", "names": ["Battey disease", "Battey disease (disorder)", "MAC - Mycobacterium avium complex", "Pulmonary Mycobacterium avium complex infection", "Pulmonary mycobacterium intracellulare infection", "bacterial pneumonia, mycobacterial avium complex", "Pulmonary infection by Mycobacterium intracellulare", "Pulmonary Mycobacterium avium-intracellulare infection", "Pulmonary mycobacterium avium-intracellulare infection", "Pulmonary Mycobacterium avium complex infection (disorder)", "Pulmonary Mycobacterium avium complex infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pulmonary mycobacterium avium-intracellulare infection", "shortest_name_length": 14}
{"curie": "UMLS:C5555608", "names": ["Ovarian MLA", "Ovarian Mesonephric-Like Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Mesonephric-Like Adenocarcinoma", "shortest_name_length": 11}
{"curie": "MONDO:0005424", "names": ["ELEPHANTIASIS", "Elephantiases", "Elephantiasis", "elephantiasis", "elephantiases", "Elephantiasis NOS", "stage III lymphedema", "lymphostatic elephantiasis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "elephantiasis", "shortest_name_length": 13}
{"curie": "MONDO:0044323", "names": ["RMNS", "RAHMAN SYNDROME", "Rahman syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rahman syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C4522125", "names": ["Stage IV Rectosigmoid Cancer", "Stage IV Rectosigmoid Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Rectosigmoid Cancer AJCC v7", "shortest_name_length": 28}
{"curie": "UMLS:C2984096", "names": ["Lung Cancer by AJCC v7 Stage", "Lung Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Cancer by AJCC v7 Stage", "shortest_name_length": 28}
{"curie": "MONDO:0006206", "names": ["fallopian tube Ca", "Fallopian Tube Cancer", "fallopian tube cancer", "Fallopian tube carcinoma", "fallopian tube carcinoma", "cancer of fallopian tube", "Cancer of Fallopian Tube", "Fallopian Tube Carcinoma", "Carcinoma of Fallopian Tube", "carcinoma of fallopian tube", "Cancer of the Fallopian Tube", "cancer of the fallopian tube", "Carcinoma of the Fallopian Tube", "carcinoma of the fallopian tube"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fallopian tube carcinoma", "shortest_name_length": 17}
{"curie": "UMLS:C0935808", "names": ["Recurrent Merkel Cell Cancer", "Recurrent Merkel Cell Carcinoma", "recurrent Merkel cell carcinoma", "Merkel cell carcinoma, recurrent", "Recurrent Neuroendocrine Carcinoma of the Skin", "recurrent neuroendocrine carcinoma of the skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Merkel Cell Carcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0006291", "names": ["jugular body cancer", "cancer of jugular body", "malignant glomus jugulare tumor", "Malignant Glomus Jugulare Tumor", "malignant jugular body neoplasm", "Malignant Glomus Jugulare Neoplasm", "malignant glomus jugulare neoplasm", "malignant neoplasm of jugular body", "malignant tumor of glomus jugulare", "Malignant Tumor of Glomus Jugulare", "malignant neoplasm of glomus jugulare", "Malignant neoplasm of glomus jugulare", "Malignant Neoplasm of Glomus Jugulare", "malignant jugulotympanic paraganglioma", "malignant tumor of the glomus jugulare", "Malignant Jugulotympanic Paraganglioma", "Metastatic Jugulotympanic Paraganglioma", "Malignant Neoplasm of the Glomus Jugulare", "malignant neoplasm of the glomus jugulare", "glomus jugulare neoplasm malignant primary", "Primary malignant neoplasm of glomus jugulare", "malignant neoplasm of glomus jugulare (diagnosis)", "Primary malignant neoplasm of glomus jugulare (disorder)", "Primary malignant neoplasm of glomus jugulare (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant jugulotympanic paraganglioma", "shortest_name_length": 19}
{"curie": "UMLS:C0160420", "names": ["injury renal", "Renal injury", "renal injury", "KIDNEY INJURY", "injury kidney", "kidney injury", "injury; kidney", "kidney; injury", "injuries renal", "injuries kidney", "injuries kidneys", "Renal injury NOS", "Injury to kidney", "Injury to Kidney", "injury to kidney", "Injury of kidney", "Renal injury, NOS", "Injury of kidney, NOS", "kidney injury (diagnosis)", "Injury of kidney (disorder)", "Unspecified injury of kidney", "Injury of kidney, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of kidney", "shortest_name_length": 12}
{"curie": "UMLS:C5670673", "names": ["Stage IB1 Cervical Cancer FIGO 2009", "Stage IB1 Cervical Carcinoma FIGO 2009"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB1 Cervical Cancer FIGO 2009", "shortest_name_length": 35}
{"curie": "MONDO:0019870", "names": ["trisomy 1pter", "Trisomy 1pter", "Distal trisomy 1p36", "distal trisomy 1p36", "distal duplication 1p36", "Distal duplication 1p36", "distal trisomy type 1p36", "Telomeric duplication 1p36", "telomeric duplication 1p36", "Distal trisomy 1p36 syndrome", "Distal trisomy 1p36 syndrome (disorder)", "Distal trisomy 1p36 syndrome (diagnosis)", "anomaly of chromosome pair distal trisomy 1p36 syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal trisomy 1p36", "shortest_name_length": 13}
{"curie": "MONDO:0002555", "names": ["schwannoma trigeminal", "Trigeminal Schwannoma", "trigeminal schwannoma", "Trigeminal schwannoma", "Trigeminal neurilemoma", "Trigeminal Neurilemmoma", "Trigeminal neurilemmoma", "trigeminal neurilemmoma", "trigeminal nerve schwannoma", "Schwannoma of Trigeminal Nerve", "schwannoma of trigeminal nerve", "fifth cranial nerve schwannoma", "Fifth Cranial Nerve Schwannoma", "Fifth Cranial Nerve Neurilemmoma", "fifth cranial nerve neurilemmoma", "Trigeminal schwannoma (disorder)", "neurilemmoma of trigeminal nerve", "Neurilemmoma of Trigeminal Nerve", "Schwannoma of Fifth Cranial Nerve", "schwannoma of fifth cranial nerve", "Schwannoma of the Trigeminal Nerve", "schwannoma of the trigeminal nerve", "neurilemmoma of fifth cranial nerve", "Neurilemmoma of Fifth Cranial Nerve", "Neurilemmoma of the Trigeminal Nerve", "neurilemmoma of the trigeminal nerve", "schwannoma of the fifth cranial nerve", "Schwannoma of the Fifth Cranial Nerve", "neurilemmoma of the fifth cranial nerve", "Neurilemmoma of the Fifth Cranial Nerve"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trigeminal schwannoma", "shortest_name_length": 21}
{"curie": "MONDO:0011326", "names": ["CTLN2", "citrin deficiency", "citrullinemia type 2", "citrullinemia type II", "adult-onset citrullinemia type 2", "adult-onset type II citrullinemia", "adult-onset citrullinemia type II", "citrullinemia, adult-onset type II", "citrullinemia, type II, ADULT-onset", "citrullinemia, type II, adult-onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "citrullinemia, type II, adult-onset", "shortest_name_length": 5}
{"curie": "MONDO:0000930", "names": ["Nodular melanoma", "nodular melanoma", "Nodular Melanoma", "melanoma nodular", "melanomas nodular", "NM - Nodular melanoma", "nodular melanoma of skin", "Nodular melanoma of skin", "nodular malignant melanoma", "Cutaneous Nodular Melanoma", "melanoma, nodular malignant", "malignant melanoma, nodular", "NM - Nodular melanoma of skin", "nodular malignant skin melanoma", "Nodular Malignant Skin Melanoma", "nodular cutaneous (skin) melanoma", "Nodular Cutaneous (Skin) Melanoma", "Nodular Malignant Melanoma of Skin", "Nodular malignant melanoma of skin", "nodular malignant melanoma of skin", "nodular melanoma of skin (diagnosis)", "nodular malignant melanoma of the skin", "Nodular Malignant Melanoma of the Skin", "Nodular melanoma (morphologic abnormality)", "nodular melanoma (morphologic abnormality)", "Nodular malignant melanoma of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nodular malignant melanoma", "shortest_name_length": 16}
{"curie": "UMLS:C0333875", "names": ["HSIL", "hsil", "high grade sil", "High grade SIL", "high-grade squamous intraepithelial lesion", "High-Grade Squamous Intraepithelial Lesion", "High grade squamous intraepithelial lesion", "High-grade squamous intraepithelial lesion", "High Grade Squamous Intraepithelial Lesion", "High-Grade Squamous Intraepithelial Lesions", "High Grade Squamous Intraepithelial Lesions", "high-grade squamous intraepithelial neoplasia", "High Grade Squamous Intraepithelial Neoplasia", "Squamous intraepithelial neoplasia, high grade", "HSIL, High Grade Squamous Intraepithelial Lesion", "HSIL, High-Grade Squamous Intraepithelial Lesions", "HSIL, High Grade Squamous Intraepithelial Lesions", "high grade squamous intraepithelial lesion (HGSIL)", "High-grade squamous intraepithelial lesion (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High-Grade Squamous Intraepithelial Lesions", "shortest_name_length": 4}
{"curie": "MONDO:0011596", "names": ["ATOD2", "FLG atopic eczema", "atopic dermatitis 2", "dermatitis, atopic, 2", "DERMATITIS, ATOPIC, 2", "dermatitis, ATOPIC, 2", "Dermatitis, Atopic, 2", "atopic dermatitis type 2", "dermatitis, Atopic, type 2", "atopic eczema caused by mutation in FLG", "dermatitis, atopic, susceptibility to, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermatitis, atopic, 2", "shortest_name_length": 5}
{"curie": "UMLS:C2699507", "names": ["Splenic B-cell lymphoma/leukemia, unclassifiable", "Splenic B-Cell Lymphoma/Leukemia, Unclassifiable"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Splenic B-Cell Lymphoma/Leukemia, Unclassifiable", "shortest_name_length": 48}
{"curie": "MONDO:0004192", "names": ["urethral Ca", "urethra cancer", "urethral cancer", "cancer of urethra", "Neoplasm malig;urethra", "malignant urethra tumor", "Malignant Urethra Tumor", "Malignant Urethral Tumor", "malignant urethral tumor", "Malignant urethral tumor", "Malignant urethral tumour", "malignant urethra neoplasm", "Malignant Tumor of Urethra", "Malignant Urethra Neoplasm", "Malignant tumor of urethra", "malignant tumor of urethra", "malignant tumour of urethra", "malignant urethral neoplasm", "Malignant Urethral Neoplasm", "Malignant tumour of urethra", "malignant neoplasm of urethra", "Malignant Neoplasm of Urethra", "Malignant neoplasm of urethra", "malignant tumor of the urethra", "Malignant Tumor of the Urethra", "malignant neoplasm of the urethra", "Malignant Neoplasm of the Urethra", "malignant neosplasm of the urethra", "Malignant tumor of urethra (disorder)", "malignant neoplasm of urethra (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urethra cancer", "shortest_name_length": 11}
{"curie": "UMLS:C1332511", "names": ["Thymic Benign Germ Cell Tumor", "Benign Mediastinal Germ Cell Tumor", "Mediastinal Benign Germ Cell Tumor", "Benign Germ Cell Tumor of Mediastinum", "Benign Mediastinal Germ Cell Neoplasm", "Benign Germ Cell Neoplasm of Mediastinum", "Benign Germ Cell Tumor of the Mediastinum", "Benign Germ Cell Neoplasm of the Mediastinum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Mediastinal Germ Cell Tumor", "shortest_name_length": 29}
{"curie": "MONDO:0010820", "names": ["JP", "PDJ", "EPDF", "PARK2", "Parkinson Disease 2", "Parkinson disease 2", "juvenile parkinsonism", "Parkinson's disease 2", "PRKN young-onset Parkinson disease", "Parkinson disease, juvenile, type 2", "Autosomal Recessive Juvenile Parkinsonism", "Juvenile Parkinsonism, Autosomal Recessive", "Parkinsonism, Juvenile, Autosomal Recessive", "autosomal recessive juvenile Parkinson disease", "Autosomal Recessive Juvenile Parkinson Disease", "Juvenile Parkinson Disease, Autosomal Recessive", "Familial Parkinson Disease, Autosomal Recessive", "PARKINSON DISEASE, JUVENILE, AUTOSOMAL RECESSIVE", "autosomal recessive juvenile Parkinson disease 2", "Parkinson Disease, Familial, Autosomal Recessive", "Parkinson disease, juvenile, autosomal recessive", "Parkinson Disease, Juvenile, Autosomal Recessive", "Parkinson disease autosomal recessive early-onset", "PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE", "Parkinson disease 2, autosomal recessive juvenile", "Parkinson Disease 2, Autosomal Recessive Juvenile", "Parkinson disease autosomal recessive, early onset", "Parkinson disease, autosomal recessive early-onset", "autosomal recessive juvenile Parkinson's disease 2", "Parkinson Disease Autosomal Recessive, Early Onset", "Parkinsonism, early-onset, with diurnal fluctuation", "Parkinsonism, Early-Onset, With Diurnal Fluctuation", "PARKINSONISM, EARLY-ONSET, WITH DIURNAL FLUCTUATION", "Parkinsonism, Early Onset, with Diurnal Fluctuation", "Parkinsonism, early onset, with diurnal fluctuation", "Chromosome 6-Linked Autosomal Recessive Parkinsonism", "Chromosome 6 Linked Autosomal Recessive Parkinsonism", "autosomal recessive juvenile Parkinson disease type 2", "young-onset Parkinson disease caused by mutation in PRKN", "Parkinson disease, autosomal recessive early-onset (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive juvenile Parkinson disease 2", "shortest_name_length": 2}
{"curie": "MONDO:0024463", "names": ["XXGD", "ODG1", "ovarian dysgenesis 1", "XX gonadal dysgenesis", "gonadal dysgenesis, XX type", "gonadal dysgenesis, 20 type", "ovarian failure, hypergonadotropic", "ovarian dysgenesis, hypergonadotropic, autosomal recessive", "ovarian dysgenesis, hypergonadotropic, with normal karyotype"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian dysgenesis 1", "shortest_name_length": 4}
{"curie": "MONDO:0020047", "names": ["autosomal recessive syndromic cerebellar ataxia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive syndromic cerebellar ataxia", "shortest_name_length": 47}
{"curie": "UMLS:C1518697", "names": ["Ovarian Dermoid Cyst with Angiosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Dermoid Cyst with Angiosarcoma", "shortest_name_length": 38}
{"curie": "MONDO:0024249", "names": ["parapsoriasis guttata", "Guttate parapsoriasis", "Parapsoriasis guttata", "lichenoides pityriasis", "pityriasis lichenoides", "Pityriasis Lichenoides", "parapsoriasis; guttata", "guttata; parapsoriasis", "Pityriasis lichenoides", "lichenoides; pityriasis", "pityriasis; lichenoides", "Parapsoriasis en gouttes", "parapsoriasis en gouttes", "acute Pityriasis Lichenoides", "Chronic lichenoid pityriasis", "pityriasis lichenoid chronic", "Pityriasis lichenoid chronic", "Pityriasis Lichenoides, acute", "Chronic Pityriasis Lichenoides", "chronic Pityriasis Lichenoides", "Pityriasis Lichenoides chronica", "Pityriasis Lichenoides Chronica", "Pityriasis Lichenoides, chronic", "pityriasis lichenoides chronica", "Pityriasis lichenoides chronica", "Pityriasis Lichenoides, Chronic", "pityriasis; lichenoides, chronica", "Pityriasis lichenoides (disorder)", "lichenoides; pityriasis, chronica", "Parapsoriasis varioliformis chronica", "PLC - Pityriasis lichenoides chronica", "Chronic lichenoid pityriasis (disorder)", "pityriasis lichenoides chronica (diagnosis)", "Pityriasis Lichenoides et Varioliformis Acuta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pityriasis lichenoides", "shortest_name_length": 21}
{"curie": "MONDO:0037251", "names": ["Banti", "INCPH", "Banti Disease", "banti syndrome", "Banti syndrome", "banti's spleen", "BANTI SYNDROME", "Banti's spleen", "Banti Syndrome", "Banti's Disease", "bantis syndrome", "Banti's syndrome", "Banti's Syndrome", "Disease, Banti's", "Syndrome, Banti's", "Congestive splenomegaly", "congestive splenomegaly", "Cirrhosis, multilobular", "Incomplete septal fibrosis", "Incomplete septal cirrhosis", "Noncirrhotic Portal Fibroses", "Fibrocongestive splenomegaly", "Cirrhosis, incomplete septal", "fibrocongestive splenomegaly", "Noncirrhotic Portal Fibrosis", "Fibrosis, Noncirrhotic Portal", "Portal Fibrosis, Noncirrhotic", "Non cirrhotic portal fibrosis", "Obliterative portal venopathy", "SPLENOMEGALY, FIBROCONGESTIVE", "Non-cirrhotic portal fibrosis", "non-cirrhotic portal fibrosis", "Idiopathic portal hypertension", "Idiopathic Portal Hypertension", "idiopathic portal hypertension", "Hypertension, Idiopathic Portal", "Idiopathic Portal Hypertensions", "Portal Hypertension, Idiopathic", "Portal fibrosis without cirrhosis", "Intrahepatic portal vein sclerosis", "Idiopathic Congestive Splenomegaly", "Congestive splenomegaly (disorder)", "Splenomegaly, Idiopathic Congestive", "Congestive Splenomegaly, Idiopathic", "Idiopathic Congestive Splenomegalies", "non-cirrhotic portal fibrosis (diagnosis)", "Idiopathic portal hypertension (disorder)", "idiopathic portal hypertension (diagnosis)", "Idiopathic Noncirrhotic Portal Hypertension", "Idiopathic Non-Cirrhotic Portal Hypertension", "Portal fibrosis without cirrhosis (disorder)", "Idiopathic non-cirrhotic portal hypertension", "Idiopathic Non Cirrhotic Portal Hypertension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congestive splenomegaly", "shortest_name_length": 5}
{"curie": "UMLS:C0014799", "names": ["Maculopapular Erythroderma", "Maculopapular Erythrodermas", "Erythroderma, Maculopapular", "Erythrodermas, Maculopapular"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Erythroderma, Maculopapular", "shortest_name_length": 26}
{"curie": "UMLS:C2827432", "names": ["Bile Acid Synthesis Defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bile Acid Synthesis Defect", "shortest_name_length": 26}
{"curie": "UMLS:C2212011", "names": ["Steroid cell tumor, malignant", "Malignant Ovarian Steroid Cell Tumor", "malignant steroid cell tumor of ovary", "malignant steroid cell tumor of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Ovarian Steroid Cell Tumor", "shortest_name_length": 29}
{"curie": "MONDO:0022171", "names": ["sweat color", "colored sweat", "Colored sweat", "chromhidrosis", "Chromhidrosis", "Coloured sweat", "colored sweat (symptom)", "Chromhidrosis (disorder)", "chromhidrosis (diagnosis)", "secretion of colored sweat", "Secretion of colored sweat", "Secretion of coloured sweat"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromhidrosis", "shortest_name_length": 11}
{"curie": "UMLS:C0854831", "names": ["Stage IV T-Cell Lymphoma", "T-cell lymphoma stage IV", "T Cell Lymphoma Stage IV", "Stage IV T Cell Lymphoma", "T-Cell Lymphoma Stage IV", "T-cell lymphoma NOS stage IV", "Stage IV T-Cell Non-Hodgkin Lymphoma", "Stage IV T-Cell Non-Hodgkin's Lymphoma", "Ann Arbor Stage IV T-Cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-cell lymphoma stage IV", "shortest_name_length": 24}
{"curie": "MONDO:0100459", "names": ["Aspermia", "ASPERMIA", "aspermia", "azospermia", "AZOSPERMIA", "AZOOSPERMIA", "azoospermia", "Azoospermia", "Sperm absent", "Azoospermatism", "Azoospermia NOS", "Aspermia (finding)", "Spermatozoa absent", "Azoospermia disorder", "Azoospermia (finding)", "Absent sperm in semen", "azoospermia (diagnosis)", "Sperm absent - azoospermia", "Azoospermia disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "azoospermia", "shortest_name_length": 8}
{"curie": "MONDO:0033925", "names": ["pediatric-onset Graves disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pediatric-onset Graves disease", "shortest_name_length": 30}
{"curie": "UMLS:C0555278", "names": ["Cerebral metastases", "cerebral metastases", "Cerebral metastasis", "cerebral metastasis", "Secondary malignant neoplasm of cerebrum", "Metastatic malignant neoplasm to cerebrum", "Metastatic malignant neoplasm of cerebrum", "Secondary malignant neoplasm of cerebrum, NOS", "Metastatic malignant neoplasm to cerebrum, NOS", "neoplasm - brain cerebrum, malignant secondary", "Metastatic malignant neoplasm to cerebrum (disorder)", "Secondary malignant neoplasm of cerebrum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebral metastasis", "shortest_name_length": 19}
{"curie": "UMLS:C3160750", "names": ["Cerebral small vessel ischemic disease", "Cerebral small vessel ischaemic disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebral small vessel ischemic disease", "shortest_name_length": 38}
{"curie": "MONDO:0021120", "names": ["functioning tumor", "functioning endocrine neoplasm", "Functioning Endocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "functioning endocrine neoplasm", "shortest_name_length": 17}
{"curie": "UMLS:C0855214", "names": ["Testicular yolk sac tumor stage II", "Stage II Testicular Yolk Sac Tumor", "Testicular yolk sac tumour stage II", "Testicular endodermal sinus tumor stage II", "Stage II Testicular Yolk Sac Tumor AJCC v7", "Stage II Testicular Yolk Sac Tumor AJCC v6", "Testicular endodermal sinus tumour stage II", "Stage II Testicular Yolk Sac Tumor AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular yolk sac tumor stage II", "shortest_name_length": 34}
{"curie": "MONDO:0019547", "names": ["Wells", "well syndrome", "Wells syndrome", "syndrome wells", "well's syndrome", "Wells' syndrome", "wells' syndrome", "eosinophilic cellulitis", "Eosinophilic cellulitis", "cellulitis; eosinophilic", "eosinophilic; cellulitis", "Eosinophilic cellulitis [Wells]", "Eosinophilic cellulitis (disorder)", "eosinophilic cellulitis (diagnosis)", "bullous cellulitis with eosinophilia", "Bullous cellulitis with eosinophilia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wells syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0006635", "names": ["Mimae Infection", "Mimae infection", "infection, Mimae", "Mimae Infections", "Mimae infections", "Infection, Mimae", "infections, Mimae", "Infections, Mimae", "acinetobacter infection", "Acinetobacter infection", "Acinetobacter Infection", "Infection, Acinetobacter", "Acinetobacter Infections", "acinetobacter infections", "Acinetobacter infections", "infection, Acinetobacter", "Infections, Acinetobacter", "infections, Acinetobacter", "Acinetobacter infectious disease", "Acinetobacter disease or disorder", "Infection caused by Acinetobacter", "Acinetobacter caused disease or disorder", "Infection caused by Acinetobacter (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acinetobacter infectious disease", "shortest_name_length": 15}
{"curie": "UMLS:C5206666", "names": ["Penile Malignant Peripheral Nerve Sheath Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Penile Malignant Peripheral Nerve Sheath Tumor", "shortest_name_length": 46}
{"curie": "UMLS:C0276933", "names": ["Schistosoma; mattheei", "Infection by Schistosoma Mattheii", "Infection by Schistosoma mattheii", "Infection caused by Schistosoma mattheii", "schistosomiasis due to Schistosoma mattheii", "Infection caused by Schistosoma mattheii (disorder)", "schistosomiasis due to Schistosoma mattheii (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infection by Schistosoma mattheii", "shortest_name_length": 21}
{"curie": "MONDO:0009562", "names": ["MANSB", "BETA-MANNOSIDOSIS", "Beta-mannosidosis", "beta mannosidosis", "beta-Mannosidosis", "beta-mannosidosis", "beta-Mannosidoses", "Beta-Mannosidosis", "beta Mannosidosis", "mannosidosis, beta", "Beta-D-mannosidosis", "Beta-mannosidase deficiency", "beta-mannosidase deficiency", "beta Mannosidase Deficiency", "BETA-MANNOSIDASE DEFICIENCY", "beta-Mannosidase Deficiency", "Lysosomal beta A Mannosidosis", "beta-Mannosidase Deficiencies", "Beta-D-mannosidosis (disorder)", "mannosidosis, BETA A, lysosomal", "MANNOSIDOSIS, BETA A, LYSOSOMAL", "Mannosidosis, beta A, Lysosomal", "lysosomal beta-mannosidase deficiency", "LYSOSOMAL BETA-MANNOSIDASE DEFICIENCY", "Lysosomal beta Mannosidase Deficiency", "Lysosomal beta-Mannosidase Deficiency", "lysosomal Beta-mannosidase deficiency", "Lysosomal beta-Mannosidase Deficiencies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "beta-mannosidosis", "shortest_name_length": 5}
{"curie": "UMLS:C4688652", "names": ["Lung Myoepithelial Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Myoepithelial Tumor", "shortest_name_length": 24}
{"curie": "UMLS:C0877248", "names": ["AE", "AdverseEvent", "side effects", "ADVERSE EVENT", "adverse event", "ADVERSE_EVENT", "adverse_event", "Adverse event", "Adverse Event", "adverse events", "Adverse event NOS", "adverse event (AE)", "adverse experience", "Adverse Experience"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adverse event", "shortest_name_length": 2}
{"curie": "MONDO:0012227", "names": ["MYP7", "Myopia 7", "MYOPIA 7", "myopia 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopia 7", "shortest_name_length": 4}
{"curie": "UMLS:C1514836", "names": ["Renal Cell Carcinoma Associated with inv(X)(p11;q12)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal Cell Carcinoma Associated with inv(X)(p11;q12)", "shortest_name_length": 52}
{"curie": "UMLS:C5401473", "names": ["Ameloblastic fibrodentinosarcoma", "Ameloblastic Fibrodentinosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ameloblastic Fibrodentinosarcoma", "shortest_name_length": 32}
{"curie": "UMLS:C0677700", "names": ["Stage II Indolent Non-Hodgkin Lymphoma", "stage II adult indolent noncontiguous non-Hodgkin lymphoma", "adult indolent noncontiguous non-Hodgkin lymphoma stage II", "adult indolent non-contiguous non-Hodgkin lymphoma stage II", "indolent non-contiguous adult non-Hodgkin lymphoma stage II", "Stage II Non-Contiguous Adult Indolent Non-Hodgkin Lymphoma", "stage II adult indolent non-contiguous non-Hodgkin lymphoma", "indolent, noncontiguous stage II adult non-Hodgkin lymphoma", "indolent non-contiguous stage II adult non-Hodgkin lymphoma", "stage II non-contiguous adult indolent non-Hodgkin lymphoma", "adult indolent non-contiguous stage II non-Hodgkin lymphoma", "Stage II Adult Indolent NonContiguous Non-Hodgkin's Lymphoma", "Adult Indolent NonContiguous Non-Hodgkin's Lymphoma Stage II", "Adult Indolent Non-Contiguous Non-Hodgkin's Lymphoma Stage II", "Adult Indolent Non-Contiguous Stage II Non-Hodgkin's Lymphoma", "Indolent Non-Contiguous Adult Non-Hodgkin's Lymphoma Stage II", "Stage II Non-Contiguous Adult Indolent Non-Hodgkin's Lymphoma", "Indolent Non-Contiguous Stage II Adult Non-Hodgkin's Lymphoma", "Stage II Adult Indolent Non-Contiguous Non-Hodgkin's Lymphoma", "Ann Arbor Stage II Non-Contiguous Adult Indolent Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Non-Contiguous Adult Indolent Non-Hodgkin Lymphoma", "shortest_name_length": 38}
{"curie": "UMLS:C4086160", "names": ["Germinomatous Germ Cell Tumor", "Childhood Germinomatous Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Germinomatous Germ Cell Tumor", "shortest_name_length": 29}
{"curie": "MONDO:0014799", "names": ["CTRCT45", "CATARACT 45", "cataract 45", "cataract type 45", "SIPA1L3 early-onset non-syndromic cataract", "early-onset non-syndromic cataract caused by mutation in SIPA1L3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 45", "shortest_name_length": 7}
{"curie": "MONDO:0005611", "names": ["BLCA", "Transitional carcinoma", "Transitional Carcinoma", "bladder urothelial cancer", "Bladder Urothelial Cancer", "Transitional Cell Carcinoma", "transitional cell carcinoma", "Transitional cell carcinoma", "Bladder Urothelial Carcinoma", "Urothelial carcinoma bladder", "bladder urothelial carcinoma", "urothelial bladder carcinoma", "transitional cell cancer bladder", "transitional cell bladder cancer", "BLADDER CANCER TRANSITIONAL CELL", "CARCINOMA, UROTHELIAL, MALIGNANT", "bladder cancer cell transitional", "Bladder transitional cell carcinoma", "Transitional cell bladder carcinoma", "Bladder Transitional Cell Carcinoma", "bladder transitional cell carcinoma", "urinary bladder urothelial carcinoma", "Urinary Bladder Urothelial Carcinoma", "carcinoma, transitional cell, bladder", "transitional cell carcinoma of bladder", "Transitional cell carcinoma of bladder", "transitional cell carcinoma of the bladder", "Transitional cell carcinoma of the bladder", "Urinary Bladder Transitional Cell Carcinoma", "bladder cancer, transitional cell carcinoma", "Urothelial Carcinoma of the Urinary Bladder", "urinary bladder transitional cell carcinoma", "urothelial carcinoma of the urinary bladder", "TCC - Transitional cell carcinoma of bladder", "TRANSITIONAL CELL CARCINOMA OF URINARY BLADDER", "Transitional cell carcinoma of bladder (disorder)", "Transitional Cell Carcinoma of the Urinary Bladder", "transitional cell carcinoma of bladder (diagnosis)", "transitional cell carcinoma of the urinary bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder transitional cell carcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0043494", "names": ["Arteritis", "arteritis", "ARTERITIS", "Arteritides", "Arteritis NOS", "Arteritis, NOS", "artery inflammation", "Arteritis (disorder)", "arteritis (diagnosis)", "arterial Inflammation", "Arterial Inflammation", "Arteritis, unspecified", "Inflammation, arterial", "inflammation of artery", "Inflammation, Arterial", "Inflammation of artery", "INFLAMMATORY ARTERY REACTION", "Inflammatory artery reaction", "Inflammatory arterial reaction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arteritis", "shortest_name_length": 9}
{"curie": "MONDO:0000255", "names": ["subcutaneous mycosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subcutaneous mycosis", "shortest_name_length": 20}
{"curie": "MONDO:0009009", "names": ["Dysplasminogenemia", "dysplasminogenemia", "DYSPLASMINOGENEMIA", "Dysplasminogenaemia", "hypoplasminogenemia", "Hypoplasminogenemia", "Hypoplasminogenaemia", "Plasminogen deficiency", "ligneous conjunctivitis", "plasminogen deficiency type I", "plasminogen deficiency type 1", "Dysplasminogenemia (disorder)", "type 1 plasminogen deficiency", "Plasminogen deficiency type 1", "plasminogen deficiency, type 1", "PLASMINOGEN DEFICIENCY, TYPE I", "plasminogen deficiency, type I", "plasminogen deficiency, type 2", "Hypoplasminogenemia (disorder)", "Plasminogen Deficiency, Type I", "dysplasminogenemia (diagnosis)", "hypoplasminogenemia (diagnosis)", "PLASMINOGEN DEFICIENCY, TYPE II", "Congenital Plasminogen Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypoplasminogenemia", "shortest_name_length": 18}
{"curie": "MONDO:0035661", "names": ["TRAF7-associated heart defect-digital anomalies-facial dysmorphism-motor and speech delay syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "TRAF7-associated heart defect-digital anomalies-facial dysmorphism-motor and speech delay syndrome", "shortest_name_length": 98}
{"curie": "MONDO:0014194", "names": ["MC3DN6", "CYC1 mitochondrial complex III deficiency", "mitochondrial Complex 3 deficiency, nuclear type 6", "mitochondrial complex III deficiency nuclear type 6", "mitochondrial complex III deficiency, nuclear type 6", "MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6", "mitochondrial complex III deficiency caused by mutation in CYC1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex III deficiency nuclear type 6", "shortest_name_length": 6}
{"curie": "MONDO:0006783", "names": ["Hemopneumothorax", "HEMOPNEUMOTHORAX", "Pneumohemothorax", "hemopneumothorax", "pneumohemothorax", "Haemopneumothorax", "haemopneumothorax", "Pneumohaemothorax", "Hemopneumothorax (disorder)", "pneumohemothorax (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemopneumothorax", "shortest_name_length": 16}
{"curie": "UMLS:C5204290", "names": ["Pseudoglandular Carcinoma of the Penis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pseudoglandular Carcinoma of the Penis", "shortest_name_length": 38}
{"curie": "MONDO:0001091", "names": ["colon lipoma", "Colon Lipoma", "Colonic Lipoma", "colonic lipoma", "Colonic lipoma", "Lipoma of Colon", "lipoma of colon", "Lipoma of the Colon", "lipoma of the colon", "Colonic lipoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lipoma of colon", "shortest_name_length": 12}
{"curie": "MONDO:0012179", "names": ["NRCLP3", "NARCOLEPSY 3", "narcolepsy 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "narcolepsy 3", "shortest_name_length": 6}
{"curie": "MONDO:0001027", "names": ["seminal vesicle gonorrhea", "gonorrhea of seminal vesicle", "Gonorrhea of seminal vesicle", "Seminal vesiculitis gonococcal", "gonococcal seminal vesiculitis", "Gonococcal seminal vesiculitis", "gonococcal seminal vesiculitis (acute)", "Gonococcal seminal vesiculitis (disorder)", "gonococcal seminal vesiculitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gonococcal seminal vesiculitis", "shortest_name_length": 25}
{"curie": "MONDO:0015295", "names": ["intractable diarrhea-choanal atresia-eye anomalies syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intractable diarrhea-choanal atresia-eye anomalies syndrome", "shortest_name_length": 59}
{"curie": "UMLS:C4683577", "names": ["Lugano Classification Stage IE Adult Non-Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage IE Adult Non-Hodgkin Lymphoma AJCC v8", "shortest_name_length": 65}
{"curie": "MONDO:0006808", "names": ["Intracranial Arterial Disease", "intracranial arterial disease", "Intracranial Arterial Diseases", "Arterial Disease, Intracranial", "Intracranial Arterial Disorder", "Intracranial Arterial Disorders", "Arterial Diseases, Intracranial", "Arterial Disorder, Intracranial", "Arterial Disorders, Intracranial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intracranial arterial disease", "shortest_name_length": 29}
{"curie": "UMLS:C0404445", "names": ["ATROPHY OVARY", "ovary atrophy", "Atrophy ovary", "atrophy; ovary", "ovary; atrophy", "ovarian atrophy", "Ovarian atrophy", "atrophy of ovary", "Atrophy of ovary", "Acquired ovarian atrophy", "ovarian atrophy acquired", "Acquired atrophy of ovary", "acquired atrophy of ovary", "Senile involution of ovary", "Acquired atrophy of ovary, NOS", "Acquired atrophy of ovary (disorder)", "Senile involution of ovary (disorder)", "acquired atrophy of ovary (diagnosis)", "Senile involution of ovary (diagnosis)", "ovarian atrophy acquired senile involution"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired atrophy of ovary", "shortest_name_length": 13}
{"curie": "MONDO:0030926", "names": ["SPGF51", "spermatogenic failure 51", "SPERMATOGENIC FAILURE 51"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 51", "shortest_name_length": 6}
{"curie": "MONDO:0100214", "names": ["Rajab interstitial lung disease with brain calcifications"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rajab interstitial lung disease with brain calcifications", "shortest_name_length": 57}
{"curie": "MONDO:0060704", "names": ["NEDSBAS", "Elhattab-Alkuraya syndrome", "ELHATTAB-ALKURAYA SYNDROME", "neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures", "NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA AND BRAIN ABNORMALITIES WITH OR WITHOUT SEIZURES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures", "shortest_name_length": 7}
{"curie": "UMLS:C4525135", "names": ["Stage IIA Rectal Cancer", "Stage IIA Rectal Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Rectal Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "MONDO:0011298", "names": ["SCZD8", "schizophrenia 8", "SCHIZOPHRENIA 8", "SCHIZOPHRENIA 8 (disorder)", "schizophrenia 8 with or without an affective disorder", "SCHIZOPHRENIA 8 WITH OR WITHOUT AN AFFECTIVE DISORDER", "SCHIZOPHRENIA SUSCEPTIBILITY LOCUS, CHROMOSOME 18-RELATED", "schizophrenia susceptibility locus, chromosome 18-related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schizophrenia 8", "shortest_name_length": 5}
{"curie": "MONDO:0017550", "names": ["humero-radial fusion, unilateral", "humero-radial synostosis, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "humero-radial synostosis, unilateral", "shortest_name_length": 32}
{"curie": "UMLS:C5206834", "names": ["Benign Parapharyngeal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Parapharyngeal Neoplasm", "shortest_name_length": 30}
{"curie": "MONDO:0005511", "names": ["janus kinase-3 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "janus kinase-3 deficiency", "shortest_name_length": 25}
{"curie": "UMLS:C0856110", "names": ["Edema aggravated", "Oedema aggravated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Edema aggravated", "shortest_name_length": 16}
{"curie": "MONDO:0044642", "names": ["hypomyelinating leukodystrophy due to hikeshi deficiency", "c11orf73-related autosomal recessive hypomyelinating leukodystrophy", "C11ORF73-related autosomal recessive hypomyelinating leukoencephalopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "c11orf73-related autosomal recessive hypomyelinating leukodystrophy", "shortest_name_length": 56}
{"curie": "MONDO:0013657", "names": ["MRD10", "autosomal dominant mental retardation 10", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 10", "mental retardation, autosomal dominant 10", "autosomal dominant intellectual disability 10", "intellectual disability, autosomal dominant 10", "mental retardation, autosomal dominant type 10", "intellectual disability, autosomal dominant type 10", "autosomal dominant intellectual developmental disorder 10", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 10", "autosomal dominant non-syndromic intellectual disability 10", "CACNG2 autosomal dominant non-syndromic intellectual disability", "autosomal dominant non-syndromic intellectual disability caused by mutation in CACNG2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 10", "shortest_name_length": 5}
{"curie": "MONDO:0017756", "names": ["disorder of pterin metabolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of pterin metabolism", "shortest_name_length": 29}
{"curie": "MONDO:0000951", "names": ["Thymus Lymphoma", "Thymic Lymphoma", "Thymus lymphoma", "thymus lymphoma", "thymic lymphoma", "lymphoma of thymus", "lymphoma of Thymus", "Lymphoma of Thymus", "lymphoma of the Thymus", "Lymphoma of the Thymus", "primary thymic lymphoma", "Primary Thymic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thymus lymphoma", "shortest_name_length": 15}
{"curie": "MONDO:0010586", "names": ["EDS5", "EDS 5", "EDS V", "X-linked EDS", "Ehlers-Danlos syndrome type V", "Ehlers-Danlos syndrome type 5", "type V Ehlers-Danlos syndrome", "Ehlers-Danlos Syndrome, Type V", "Ehlers-Danlos syndrome, type 5", "Ehlers-Danlos syndrome, type V", "X-linked Ehlers-Danlos syndrome", "Ehlers-Danlos syndrome, X-linked", "Ehlers-Danlos syndrome, mild x-linked", "Cutis hyperelastica V, sex-linked type", "Ehlers-Danlos syndrome, type 5 (disorder)", "Ehlers-Danlos syndrome, type V (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked Ehlers-Danlos syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0013528", "names": ["MRT14", "mental retardation, autosomal recessive 14", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 14", "mental retardation, autosomal recessive type 14", "intellectual disability, autosomal recessive 14", "intellectual disability, autosomal recessive type 14", "autosomal recessive intellectual developmental disorder 14", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 14", "TECR autosomal recessive non-syndromic intellectual disability", "autosomal recessive non-syndromic intellectual disability caused by mutation in TECR"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 14", "shortest_name_length": 5}
{"curie": "MONDO:0060729", "names": ["EPP2", "PROTOPORPHYRIA, ERYTHROPOIETIC, 2", "protoporphyria, erythropoietic, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "protoporphyria, erythropoietic, 2", "shortest_name_length": 4}
{"curie": "MONDO:0017930", "names": ["mixed sclerosing bone dystrophy with extra-skeletal manifestations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed sclerosing bone dystrophy with extra-skeletal manifestations", "shortest_name_length": 66}
{"curie": "MONDO:0017853", "names": ["HP", "alveolitis", "Bagpipe lung", "Allergic alveolitis", "allergic alveolitis", "Alveolitis allergic", "Allergic Alveolitis", "alveolitis allergic", "ALVEOLITIS ALLERGIC", "PNEUMONITIS ALLERGIC", "Allergic Pneumonitis", "allergic; alveolitis", "Pneumonitis allergic", "alveolitis; allergic", "Allergic pneumonitis", "Alveolitis, allergic", "allergic pneumonitis", "Allergic alveolitis, NOS", "Allergic pneumonitis, NOS", "Hypersensitivity pneumonia", "exogen allergic alveolitis", "hypersensitivity pneumonia", "HYPERSENSITIVITY PNEUMONITIS", "Hypersensitivity Pneumonitis", "Pneumonitis hypersensitivity", "hypersensitivity pneumonitis", "allergic form of pneumonitis", "Hypersensitivity pneumonitis", "Alveolitis extrinsic allergic", "Pneumonitis, Hypersensitivity", "pneumonitis; hypersensitivity", "Extrinsic Allergic Alveolitis", "hypersensitivity; pneumonitis", "extrinsic allergic alveolitis", "PNEUMONITIS, HYPERSENSITIVITY", "Extrinsic allergic alveolitis", "Alveolitis, Extrinsic Allergic", "Hypersensitivity Pneumonitides", "Allergic Alveolitis, Extrinsic", "Extrinsic alveolitis, allergic", "alveolitis, extrinsic allergic", "ALVEOLITIS, EXTRINSIC ALLERGIC", "Hypersensitivity pneumonia, NOS", "Pneumonitides, Hypersensitivity", "Extrinsic Allergic Alveolitides", "Hypersensitivity pneumonitis NOS", "Alveolitides, Extrinsic Allergic", "Allergic Alveolitides, Extrinsic", "Allergic interstitial pneumonitis", "Hypersensitivity pneumonitis, NOS", "allergic interstitial pneumonitis", "Extrinsic allergic alveolitis, NOS", "PNEUMONITIS, ALLERGIC INTERSTITIAL", "EAA - Extrinsic allergic alveolitis", "Allergic alveolitis (extrinsic) NOS", "Allergic interstitial pneumonitis, NOS", "Extrinsic allergic alveolitis (disorder)", "hypersensitivity pneumonitis (diagnosis)", "Extrinsic allergic bronchiolo-alveolitis", "Extrinsic allergic bronchiolo-alveolitis, NOS", "Unspecified allergic alveolitis and pneumonitis", "extrinsic allergic pneumonia hypersensitivity pneumonitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypersensitivity pneumonitis", "shortest_name_length": 2}
{"curie": "UMLS:C1167677", "names": ["infrequent bowel movement", "Infrequent bowel movements", "infrequent bowel movements"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infrequent bowel movements", "shortest_name_length": 25}
{"curie": "UMLS:C4682583", "names": ["Stage III Uterine Corpus Adenosarcoma", "Stage III Uterine Corpus Adenosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Uterine Corpus Adenosarcoma AJCC v8", "shortest_name_length": 37}
{"curie": "MONDO:0032568", "names": ["IDDMSSD", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY", "intellectual developmental disorder with macrocephaly, seizures, and speech delay"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder with macrocephaly, seizures, and speech delay", "shortest_name_length": 7}
{"curie": "MONDO:0005342", "names": ["IGAN", "BERGER DISEASE", "Berger Disease", "disease berger", "berger disease", "IgA Nephropathy", "nephropathy IgA", "Bergers disease", "IGA Nephropathy", "Bergers Disease", "nephropathy iga", "bergers disease", "IGA NEPHROPATHY", "IgA nephropathy", "iga nephropathy", "Berger's Disease", "berger's disease", "nephropathy; IgA", "NEPHROPATHY, IGA", "Nephropathy, IGA", "IgA; nephropathy", "Berger's disease", "Iga Nephropathy 1", "IGA Type Nephritis", "Nephropathy 1, Iga", "NEPHRITIS, IgA TYPE", "Nephritis, IGA Type", "primary IgA nephritis", "IGA Glomerulonephritis", "IGA glomerulonephritis", "glomerulonephritis iga", "iga glomerulonephritis", "IgA glomerulonephritis", "IgAN - IgA nephropathy", "Primary IgA nephropathy", "primary IgA nephropathy", "Glomerulonephritis, IGA", "glomerulonephritis; IgA", "Focal glomerulonephritis", "Glomerulonephritis focal", "GLOMERULONEPHRITIS FOCAL", "focal glomerulonephritis", "glomerulonephritis focal", "Focal Glomerulonephritis", "Glomerulonephritides, IGA", "Mesangial IgA/IgG disease", "IgA nephropathy (diagnosis)", "Immunoglobulin A Nephropathy", "segmental glomerulonephritis", "Immunoglobulin A nephropathy", "Nephropathy, Immunoglobulin A", "IgA/IgG nephropathy of Berger", "berger's IgA or IgG nephropathy", "Berger's IgA or IgG nephropathy", "IgA deposition in the glomerulus", "primary IgA nephritis (diagnosis)", "Primary IgA nephropathy (diagnosis)", "Primary immunoglobulin A nephropathy", "Immunoglobulin A nephropathy (disorder)", "Primary immunoglobulin A nephropathy (disorder)", "IDIOPATHIC FOCAL NEPHRITIS WITH MESANGIAL DEPOSITS OF IGA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IgA glomerulonephritis", "shortest_name_length": 4}
{"curie": "UMLS:C4683472", "names": ["Thyroid Gland Medullary Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Medullary Carcinoma by AJCC v8 Stage", "shortest_name_length": 50}
{"curie": "MONDO:0013520", "names": ["DKCB3", "autosomal recessive dyskeratosis congenita 3", "DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 3", "Dyskeratosis Congenita, Autosomal Recessive 3", "dyskeratosis congenita, autosomal recessive 3", "dyskeratosis congenita, autosomal recessive type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyskeratosis congenita, autosomal recessive 3", "shortest_name_length": 5}
{"curie": "UMLS:C3272523", "names": ["Small Intestinal Follicular Lymphoma", "Primary Small Intestinal Follicular Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Intestinal Follicular Lymphoma", "shortest_name_length": 36}
{"curie": "MONDO:0018922", "names": ["CAS", "CAD", "cold antibody disease", "cold agglutinin disease", "cold agglutinin syndrome", "cold antibody hemolytic anemia", "Chronic cold agglutinin disease", "chronic cold agglutinin disease", "anemia, hemolytic, cold antibody", "Chronic cold agglutinin disease (disorder)", "disease (or disorder); cold, hemagglutinin (chronic)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cold agglutinin disease", "shortest_name_length": 3}
{"curie": "UMLS:C0281980", "names": ["Injury;skin", "Skin Injury", "injury skin", "Skin injury", "skin injury", "injury; skin", "injuries skin", "Injury of skin", "injury to skin", "Skin injury NOS", "Injury of integument", "injury of integument", "Injury of integument (disorder)", "injury of integument (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of integument", "shortest_name_length": 11}
{"curie": "UMLS:C1333982", "names": ["Hepatoblastoma with Pure Fetal Epithelial Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatoblastoma with Pure Fetal Epithelial Differentiation", "shortest_name_length": 57}
{"curie": "UMLS:C4763953", "names": ["Preterm Birth Complication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Preterm Birth Complication", "shortest_name_length": 26}
{"curie": "MONDO:0016182", "names": ["qualitative or quantitative defects of protein POMGNT1", "qualitative or quantitative defects of protein O-mannose beta1, 2N-acetylglucosaminyltransferase"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of protein O-mannose beta1, 2N-acetylglucosaminyltransferase", "shortest_name_length": 54}
{"curie": "MONDO:0017520", "names": ["symbrachydactyly of hand and foot, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "symbrachydactyly of hand and foot, bilateral", "shortest_name_length": 44}
{"curie": "MONDO:0000473", "names": ["Arteriopath", "arteriopathy", "Arteriopathy", "artery disease", "artery diseases", "artery disorder", "Arterial Disease", "arterial disease", "Arterial disease", "artery; disorder", "artery disorders", "Arterial Disorder", "Arterial disorder", "arterial diseases", "arterial disorder", "disease of artery", "Disorder of artery", "disorder of artery", "arterial disorders", "Arterial disorder NOS", "Arteriopathic disease", "Disease of artery, NOS", "Disorder of artery, NOS", "DISEASES OF THE ARTERIES", "diseases of the arteries", "vascular arterial disease", "Arterial vascular disease", "arterial vascular disease", "artery disease or disorder", "Generalised arterial disease", "Generalized arterial disease", "Disorder of artery (disorder)", "disease (or disorder); artery", "disease or disorder of artery", "disorder of artery (diagnosis)", "Disease of Arteries, Arterioles and Capillaries"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arterial disorder", "shortest_name_length": 11}
{"curie": "UMLS:C1881034", "names": ["Head and Neck Nevus", "Nevus of Head and Neck"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Head and Neck Nevus", "shortest_name_length": 19}
{"curie": "UMLS:C4521645", "names": ["stage IVB esophageal cancer", "Stage IVB Esophageal Adenocarcinoma", "Clinical Stage IVB Esophageal Adenocarcinoma AJCC v8", "clinical stage IVB esophageal adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage IVB Esophageal Adenocarcinoma AJCC v8", "shortest_name_length": 27}
{"curie": "MONDO:0012608", "names": ["DSMA4", "dSMA4", "Dsma4", "Distal spinal muscular atrophy type 4", "distal spinal muscular atrophy type 4", "spinal muscular atrophy, distal, autosomal recessive, 4", "Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4", "SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 4", "Autosomal recessive distal spinal muscular atrophy type 4", "autosomal recessive distal spinal muscular atrophy type 4", "spinal muscular atrophy, distal, autosomal recessive, type 4", "Autosomal recessive lower motor neuron disease with childhood onset", "autosomal recessive lower motor neuron disease with childhood onset", "Autosomal recessive lower motor neuron disease with childhood onset (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive lower motor neuron disease with childhood onset", "shortest_name_length": 5}
{"curie": "MONDO:0011523", "names": ["BBS6", "Bardet-Biedl syndrome 6", "Bardet-Biedl Syndrome 6", "BARDET-BIEDL SYNDROME 6", "Bardet-Biedl syndrome type 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bardet-Biedl syndrome 6", "shortest_name_length": 4}
{"curie": "UMLS:C0262417", "names": ["CHRONIC ACUTE PANCREATITIS", "acute on chronic pancreatitis", "Acute on chronic pancreatitis", "Pancreatitis acute on chronic", "PANCREATITIS ACUTE ON CHRONIC", "Acute and chronic pancreatitis", "Acute on chronic pancreatitis (disorder)", "acute on chronic pancreatitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute on chronic pancreatitis", "shortest_name_length": 26}
{"curie": "MONDO:0023206", "names": ["Functioning PNET", "functioning PNET", "syndromic pancreatic NET", "Syndromic Pancreatic NET", "Functional Pancreatic NET", "functional pancreatic NET", "Functioning Pancreatic NET", "Functioning pancreatic NET", "functioning pancreatic NET", "Functional Neuroendocrine Tumor", "Functioning Pancreatic Endocrine Tumor", "functioning pancreatic endocrine tumor", "Syndromic Pancreatic Neuroendocrine Tumor", "syndromic pancreatic neuroendocrine tumor", "Functional Pancreatic Neuroendocrine Tumor", "functional pancreatic neuroendocrine tumor", "Functioning pancreatic neuroendocrine tumor", "functioning pancreatic neuroendocrine tumor", "Functioning Pancreatic Neuroendocrine Tumor", "functioning neuroendocrine tumor of pancreas", "Functioning neuroendocrine tumor of pancreas", "functioning well-differentiated pancreatic NEN", "Functioning well-differentiated pancreatic NEN", "functioning well-differentiated NEN of pancreas", "Functioning well-differentiated NEN of pancreas", "Functioning Well Differentiated Pancreatic Endocrine Tumor", "functioning well differentiated pancreatic endocrine tumor", "functioning well differentiated pancreatic endocrine neoplasm", "Functioning Well Differentiated Pancreatic Endocrine Neoplasm", "functioning well-differentiated pancreatic neuroendocrine neoplasm", "Functioning well-differentiated pancreatic neuroendocrine neoplasm", "Functioning well-differentiated neuroendocrine neoplasm of pancreas", "functioning well-differentiated neuroendocrine neoplasm of pancreas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "functional pancreatic neuroendocrine tumor", "shortest_name_length": 16}
{"curie": "MONDO:0004879", "names": ["choroidal senile atrophy", "senile atrophy of choroid", "Senile atrophy of choroid", "Senile atrophy of choroid (disorder)", "choroidal senile atrophy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "senile atrophy of choroid", "shortest_name_length": 24}
{"curie": "UMLS:C1335024", "names": ["Non-Neoplastic Nervous System Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Nervous System Disorder", "shortest_name_length": 38}
{"curie": "UMLS:C1335937", "names": ["Secondary Cerebral Hodgkin Lymphoma", "Secondary Cerebral Hodgkin's Disease", "Secondary Cerebral Hodgkin's Lymphoma", "Metastatic Hodgkin's Lymphoma to Cerebral Hemisphere", "Metastatic Hodgkin Lymphoma to the Cerebral Hemisphere", "Metastatic Hodgkin Lymphoma in the Cerebral Hemisphere"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary Cerebral Hodgkin Lymphoma", "shortest_name_length": 35}
{"curie": "UMLS:C2721559", "names": ["Osmotic demyelination syndrome", "ODS - osmotic demyelination syndrome", "Osmotic demyelination syndrome (disorder)", "Central pontine myelinolysis and extrapontine myelinolysis", "CPM (central pontine myelinolysis) and EPM (extrapontine myelinolysis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Osmotic demyelination syndrome", "shortest_name_length": 30}
{"curie": "MONDO:0008976", "names": ["Chondroitin-6-Sulfaturia, Defective Cellular Immunity, Nephrotic Syndrome", "chondroitin-6-Sulfaturia, defective cellular immunity, nephrotic syndrome", "chondroitin-6-sulfaturia, defective cellular immunity, nephrotic syndrome", "CHONDROITIN-6-SULFATURIA, DEFECTIVE CELLULAR IMMUNITY, NEPHROTIC SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chondroitin-6-sulfaturia, defective cellular immunity, nephrotic syndrome", "shortest_name_length": 73}
{"curie": "MONDO:0015132", "names": ["immunodeficiency predominantly affecting antibody production"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency predominantly affecting antibody production", "shortest_name_length": 60}
{"curie": "UMLS:C5237197", "names": ["Unresectable Pancreatic Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Pancreatic Neuroendocrine Neoplasm", "shortest_name_length": 47}
{"curie": "UMLS:C5419757", "names": ["Unresectable Oral Cavity Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Oral Cavity Squamous Cell Carcinoma", "shortest_name_length": 48}
{"curie": "MONDO:0013308", "names": ["NSLL", "Cbl syndrome", "CBL SYNDROME", "CBL syndrome", "CBL Syndrome", "CBL-related disorder", "Noonan-like syndrome", "Cbl mutation-associated syndrome", "CBL MUTATION-ASSOCIATED SYNDROME", "CBL Mutation-Associated Syndrome", "CBL (Cbl proto-oncogene) syndrome", "Noonan syndrome-like disorder with JMML", "NOONAN SYNDROME-LIKE DISORDER WITH JUVENILE MYELOMONOCYTIC LEUKEMIA", "Noonan syndrome-like disorder with juvenile myelomonocytic leukemia", "Noonan syndrome-like disorder with juvenile myelomonocytic leukaemia", "Noonan syndrome-like disorder with juvenile myelomonocytic leukemia (disorder)", "Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia", "NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA", "Noonan Syndrome-Like Disorder with or without Juvenile Myelomonocytic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CBL-related disorder", "shortest_name_length": 4}
{"curie": "UMLS:C1558746", "names": ["Intraoperative skin injury", "Intraoperative Skin Injury", "intraoperative skin injury", "intraoperative skin injury (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraoperative skin injury", "shortest_name_length": 26}
{"curie": "MONDO:0017966", "names": ["46,XY disorder of gonadal development"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XY disorder of gonadal development", "shortest_name_length": 37}
{"curie": "UMLS:C1336473", "names": ["Ovarian Polyembryoma Stage I", "Stage I Ovarian Polyembryoma", "Stage I Ovarian Polyembryoma AJCC v7", "Stage I Ovarian Polyembryoma AJCC v6", "Stage I Ovarian Polyembryoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Ovarian Polyembryoma AJCC v6 and v7", "shortest_name_length": 28}
{"curie": "MONDO:0003712", "names": ["Angiokeratoma of Mibelli", "angiokeratoma of mibelli", "Angiokeratoma of Mibelli (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angiokeratoma of mibelli", "shortest_name_length": 24}
{"curie": "UMLS:C0162629", "names": ["Oxyurida Infection", "Oxyurida Infections", "Infection, Oxyurida", "Infections, Oxyurida"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oxyurida Infections", "shortest_name_length": 18}
{"curie": "UMLS:C1332524", "names": ["Benign Luteinized Ovarian Thecoma", "Benign Ovarian Luteinized Thecoma", "Benign Luteinized Thecoma of Ovary", "Benign Luteinized Thecoma of the Ovary", "Benign Ovarian Luteinized Thecal Cell Tumor", "Benign Luteinized Thecal Cell Tumor of Ovary", "Benign Ovarian Luteinized Thecal Cell Neoplasm", "Benign Luteinized Thecal Cell Neoplasm of Ovary", "Benign Luteinized Thecal Cell Tumor of the Ovary", "Benign Luteinized Thecal Cell Neoplasm of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Ovarian Luteinized Thecoma", "shortest_name_length": 33}
{"curie": "UMLS:C1609506", "names": ["Reaction to preservatives"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reaction to preservatives", "shortest_name_length": 25}
{"curie": "UMLS:C1335492", "names": ["Primary Systemic ALKoma", "Primary Systemic ALK-Positive ALCL", "Primary Systemic ALK-Positive Anaplastic Large Cell Lymphoma", "Primary Systemic Anaplastic Large Cell Lymphoma, ALK-Positive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Systemic Anaplastic Large Cell Lymphoma, ALK-Positive", "shortest_name_length": 23}
{"curie": "MONDO:0005191", "names": ["iv melanoma stage", "melanoma stage iv", "stage iv melanoma", "melanoma metastatic", "Metastatic Melanoma", "Melanoma metastatic", "metastatic melanoma", "Metastatic melanoma", "metastatic; melanoma", "melanoma; metastatic", "melanoma, metastatic", "Metastatic malignant melanoma", "metastatic malignant melanoma", "malignant melanoma metastatic", "Malignant melanoma, metastatic", "metastatic; melanoma, unspecified site", "melanoma; metastatic, unspecified site", "Metastatic malignant melanoma (disorder)", "metastatic malignant melanoma (diagnosis)", "Malignant melanoma, metastatic (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metastatic melanoma", "shortest_name_length": 17}
{"curie": "MONDO:0009169", "names": ["EFE", "Elastomyofibrosis", "elastomyofibrosis", "Endocardial fibroelastosis", "endocardial fibroelastosis", "Endocardial Fibroelastoses", "Endocardial Fibroelastosis", "ENDOCARDIAL FIBROELASTOSIS", "Fibroelastosis, Endocardial", "Fibroelastoses, Endocardial", "FIBROELASTOSIS, ENDOCARDIUM", "endomyocardial fibroelastosis", "Endomyocardial fibroelastosis", "Endomyocardial Fibroelastosis", "EFE - Endocardial fibroelastosis", "Endocardial fibroelastosis (disorder)", "endocardial fibroelastosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endocardial fibroelastosis", "shortest_name_length": 3}
{"curie": "MONDO:0007661", "names": ["TS", "GTS", "Tourette", "tic de Guinon", "de la Tourette", "psychogenic tics", "Tourette Disease", "Tourette disease", "Guinon's disease", "maladie des tics", "Psychogenic tics", "TOURETTE SYNDROME", "TOURETTE DISORDER", "Tourette Syndrome", "Tourette disorder", "Tourettes Disease", "syndrome tourette", "Tourette Disorder", "tourette syndrome", "SYNDROME TOURETTE", "tourette disorder", "disorder tourette", "tourettes disease", "Tourette syndrome", "tourettes disorder", "tourette's disease", "Tourette's Disease", "syndrome tourettes", "chronic motor tics", "Syndrome, Tourette", "Chronic Motor Tics", "CHRONIC MOTOR TICS", "tourettes syndrome", "Tourettes syndrome", "Tourettes Syndrome", "TOURETTES SYNDROME", "Tourettes Disorder", "syndromes tourette", "syndrome tourette's", "Tourette's disorder", "motor; tic, chronic", "chronic; tic, motor", "tourette's disorder", "tic; chronic, motor", "tourette's syndrome", "tic; motor, chronic", "syndromes tourettes", "Tourette's Disorder", "tic; de la Tourette", "Tourette's syndrome", "Tourette's Syndrome", "de la Tourette; tic", "syndrome tourettes's", "GILLES DE LA TOURETTE", "de gilles la tourette", "Gilles de la Tourette", "gilles de la tourette", "de gilles la tourettes", "motor-verbal tic disorder", "Motor-verbal tic disorder", "motor-verbal tic disorders", "Guinon's myospasia impulsiva", "gilles de la tourette syndrome", "GILLES DE LA TOURETTE SYNDROME", "Gilles de la Tourette syndrome", "Gilles de la Tourette Disorder", "SYNDROME GILLES DE LA TOURETTE", "gilles de la tourette disorder", "Syndrome Gilles de la Tourette", "Gilles de la Tourette Syndrome", "Gilles de la Tourettes syndrome", "Tourette's syndrome (diagnosis)", "Gilles de la Tourette's Disease", "Gilles De 50A Tourette syndrome", "Gilles De La Tourette's Syndrome", "gilles de la tourette's syndrome", "Gilles de la Tourette's syndrome", "Gilles de la Tourette's disorder", "tourette's syndrome gilles de la", "Chronic Motor and Vocal Tic Disorder", "tic; combined vocal and multiple motor", "combined; tic, vocal and multiple motor", "Gilles de la Tourette's syndrome (disorder)", "Combined Vocal and Multiple Motor Tic Disorder", "Combined Multiple Motor and Vocal Tic Disorder", "Combined vocal and multiple motor tic disorder", "Tic Disorder, Combined Vocal and Multiple Motor", "Multiple Motor and Vocal Tic Disorder, Combined", "Combined vocal and multiple motor tic disorder [de la Tourette]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tourette syndrome", "shortest_name_length": 2}
{"curie": "UMLS:C0948309", "names": ["pseudohyperkalemia", "Pseudohyperkalemia", "Pseudohyperkalaemia", "pseudohyperkalemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pseudohyperkalaemia", "shortest_name_length": 18}
{"curie": "UMLS:C0862039", "names": ["Stage II B-Lymphoblastic Lymphoma", "Stage II B Lymphoblastic Lymphoma", "Precursor B-Lymphoblastic Lymphoma Stage II", "Stage II Precursor B-Lymphoblastic Lymphoma", "Precursor B-lymphoblastic lymphoma stage II", "Ann Arbor Stage II B Lymphoblastic Lymphoma", "Precursor B-lymphoblastic lymphoma NOS stage II", "Precursor B-lymphoblastic lymphoma/leukemia stage II", "Precursor B-lymphoblastic lymphoma/leukaemia stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Precursor B-lymphoblastic lymphoma stage II", "shortest_name_length": 33}
{"curie": "MONDO:0045012", "names": ["steroid metabolism disease", "steroid metabolism disorder", "Disorder of steroid metabolism", "disorder of steroid metabolism", "DISORDERS OF STEROID METABOLISM", "steroid metabolic process disease", "Disorder of steroid metabolism, NOS", "disorder of steroid metabolic process", "Disorder of steroid metabolism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "steroid metabolism disease", "shortest_name_length": 26}
{"curie": "MONDO:0001725", "names": ["penile lichen Sclerosus", "Penile Lichen Sclerosus", "induratio penis plastica", "Induratio penis plastica", "lichen Sclerosus of penis", "Lichen Sclerosus of Penis", "Lichen sclerosus of penis", "Lichen Sclerosus of the Penis", "lichen Sclerosus of the penis", "balanitis obliterans xerotica", "Balanitis xerotica obliterans", "Balanitis Xerotica Obliterans", "balanitis xerotica obliterans", "xerotica obliterans; balanitis", "balanitis; xerotica obliterans", "Lichen sclerosus of glans penis", "BXO - Balanitis xerotica obliterans", "Lichen sclerosus of penis (disorder)", "Balanitis xerotica obliterans (disorder)", "balanitis xerotica obliterans (diagnosis)", "Lichen sclerosus et atrophicus of glans penis and prepuce"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "balanitis xerotica obliterans", "shortest_name_length": 23}
{"curie": "MONDO:0019435", "names": ["polyarticular JIA, RF+", "Polyarticular JIA, RF+", "polyarthritis with rheumatoid factor", "rheumatoid factor-positive polyarticular JIA", "polyarticular juvenile idiopathic arthritis, RF+", "Polyarticular Juvenile Idiopathic Arthritis, RF+", "polyarticular juvenile idiopathic arthritis RF positive", "juvenile idiopathic rheumatoid factor-positive polyarthritis", "rheumatoid factor-positive polyarticular juvenile idiopathic arthritis", "polyarticular juvenile idiopathic arthritis, rheumatoid factor positive", "Polyarticular Juvenile Idiopathic Arthritis, Rheumatoid Factor Positive", "polyarticular juvenile idiopathic arthritis, rheumatoid Factor Positive", "polyarticular juvenile idiopathic arthritis with positive rheumatoid factor", "polyarticular juvenile idiopathic arthritis with positive rheumatoid factor (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rheumatoid factor-positive polyarticular juvenile idiopathic arthritis", "shortest_name_length": 22}
{"curie": "UMLS:C2698832", "names": ["Plasmablastic Lymphoma of the Oral Cavity", "Plasmablastic Lymphoma of the Oral Mucosa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Plasmablastic Lymphoma of the Oral Mucosa", "shortest_name_length": 41}
{"curie": "MONDO:0004416", "names": ["plasmacytoid/signet ring cell bladder carcinoma", "plasmacytoid variant infiltrating bladder urothelial carcinoma", "Infiltrating Bladder Urothelial Carcinoma, Plasmacytoid Variant", "infiltrating bladder urothelial carcinoma, plasmacytoid variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "plasmacytoid variant infiltrating bladder urothelial carcinoma", "shortest_name_length": 47}
{"curie": "MONDO:0003365", "names": ["esophagus leiomyosarcoma", "Esophagus Leiomyosarcoma", "Esophageal Leiomyosarcoma", "esophageal leiomyosarcoma", "oesophagus leiomyosarcoma", "leiomyosarcoma of esophagus", "Leiomyosarcoma of esophagus", "Leiomyosarcoma of Esophagus", "leiomyosarcoma of oesophagus", "Leiomyosarcoma of oesophagus", "Leiomyosarcoma of the Esophagus", "leiomyosarcoma of the esophagus", "Leiomyosarcoma of esophagus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophagus leiomyosarcoma", "shortest_name_length": 24}
{"curie": "MONDO:0019756", "names": ["Cingulosynapsis", "Olfactory aplasia", "Lobar Holoprosencephaly", "Lobar holoprosencephaly", "lobar holoprosencephaly", "Holoprosencephaly, Lobar", "Lobar Holoprosencephalies", "Holoprosencephalies, Lobar", "Lobar holoprosencephaly (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lobar holoprosencephaly", "shortest_name_length": 15}
{"curie": "MONDO:0001848", "names": ["Morgagni cataract", "Morgagnian cataract", "cataract morgagnian", "Hypermature cataract", "cataract hypermature", "hypermature cataract", "Cataract, hypermature", "morgagnian; type cataract", "cataract; Morgagnian type", "Morgagnian cataract (disorder)", "Morgagni; type senile cataract", "Morgagnian cataract (diagnosis)", "Hypermature cataract (disorder)", "hypermature cataract (diagnosis)", "Senile cataract, morgagnian type", "senile cataract; Morgagnian type", "cataract; senile, Morgagnian type", "hypermature cataract (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Morgagni cataract", "shortest_name_length": 17}
{"curie": "UMLS:C0585954", "names": ["Vocal Cord Dysplasia", "Dysplasia of Vocal Cord", "dysplasia of vocal cord", "Dysplasia of vocal cord", "Dysplasia of vocal cord (disorder)", "dysplasia of vocal cord (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dysplasia of vocal cord", "shortest_name_length": 20}
{"curie": "MONDO:0007601", "names": ["FMF autosomal dominant", "Fmf, autosomal dominant", "FMF, AUTOSOMAL DOMINANT", "familial Mediterranean fever, AD", "FMF autosomal dominant (diagnosis)", "familial Mediterranean fever autosomal dominant", "Familial Mediterranean Fever, Autosomal Dominant", "FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL DOMINANT", "familial Mediterranean fever, autosomal dominant", "[OBSOLETE] Familial Mediterranean Fever, Autosomal Dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial Mediterranean fever, autosomal dominant", "shortest_name_length": 22}
{"curie": "UMLS:C1334413", "names": ["DIN 1C", "DCIS Grade 1", "Low-Grade DCIS", "Low Grade Ductal Breast Carcinoma In Situ", "Breast Ductal Carcinoma In Situ, Low Grade", "Ductal Intraepithelial Neoplasia, Grade 1C", "Low-Grade Ductal Carcinoma In Situ of Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Ductal Carcinoma In Situ, Low Grade", "shortest_name_length": 6}
{"curie": "MONDO:0008286", "names": ["crossed polydactyly", "Crossed polysyndactyly", "crossed polysyndactyly", "polysyndactyly, crossed", "Polysyndactyly, Crossed", "POLYSYNDACTYLY, CROSSED", "Crossed polysyndactyly (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "crossed polysyndactyly", "shortest_name_length": 19}
{"curie": "UMLS:C4288813", "names": ["Pyloric Gland Metaplasia", "Lobular Endocervical Glandular Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lobular Endocervical Glandular Hyperplasia", "shortest_name_length": 24}
{"curie": "MONDO:0001743", "names": ["paranasal sinus lymphoma", "Accessory Sinus Lymphoma", "accessory sinus lymphoma", "Paranasal Sinus Lymphoma", "lymphoma of paranasal sinus", "Lymphoma of Accessory sinus", "lymphoma of accessory sinus", "Lymphoma of Accessory Sinus", "Lymphoma of Paranasal Sinus", "lymphoma of the accessory sinus", "lymphoma of the paranasal sinus", "Lymphoma of the Accessory Sinus", "Lymphoma of the Paranasal Sinus", "primary paranasal sinus lymphoma", "Primary Paranasal Sinus Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paranasal sinus lymphoma", "shortest_name_length": 24}
{"curie": "MONDO:0015075", "names": ["THCA", "thyroid cancer", "Thyroid cancer", "Thyroid Cancer", "Thyroid Cancers", "Cancer, Thyroid", "Cancers, Thyroid", "Thyroid Carcinoma", "cancer of thyroid", "Carcinoma thyroid", "thyroid carcinoma", "THYROID CARCINOMA", "Cancer of Thyroid", "carcinoma thyroid", "Thyroid carcinoma", "CARCINOMA THYROID", "Carcinoma, Thyroid", "Thyroid Carcinomas", "Thyroid cancer, NOS", "Carcinomas, Thyroid", "Carcinoma of Thyroid", "Carcinoma of thyroid", "CARCINOMA OF THYROID", "carcinoma of thyroid", "thyroid gland cancer", "Thyroid Gland Cancer", "cancer of the thyroid", "Thyroid carcinoma NOS", "Cancer of the Thyroid", "Thyroid gland--Cancer", "thyroid gland carcinoma", "Thyroid Gland Carcinoma", "Carcinoma;thyroid gland", "carcinoma thyroid gland", "carcinoma of the thyroid", "Carcinoma of the Thyroid", "Carcinoma of Thyroid Gland", "carcinoma of thyroid gland", "thyroid cancer (diagnosis)", "head and neck cancer, Thyroid", "thyroid carcinoma (diagnosis)", "head and neck cancer, thyroid", "carcinoma of the thyroid gland", "Carcinoma of the Thyroid Gland", "Malignant epithelial neoplasm of thyroid", "Malignant epithelial neoplasm of thyroid (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid gland carcinoma", "shortest_name_length": 4}
{"curie": "UMLS:C0948352", "names": ["Injury asphyxiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury asphyxiation", "shortest_name_length": 19}
{"curie": "MONDO:0004099", "names": ["benign teratoma", "Benign Teratoma", "Benign teratoma", "TERATOMA BENIGN", "Cystic teratoma", "Teratoma benign", "Teratoma, benign", "Teratoma, Benign", "Teratoma, Cystic", "Teratoma, Mature", "Benign Teratomas", "Teratomas, Benign", "Adult cystic teratoma", "Adult Cystic Teratoma", "adult cystic teratoma", "Differentiated teratoma", "Teratoma, differentiated", "cystic teratoma of adults", "Teratoma, differentiated type", "Teratoma, benign (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult cystic teratoma", "shortest_name_length": 15}
{"curie": "UMLS:C0346348", "names": ["Malignant Orbit Hemangiopericytoma", "Malignant Orbital Hemangiopericytoma", "Malignant hemangiopericytoma of orbit", "malignant hemangiopericytoma of orbit", "Malignant Hemangiopericytoma of Orbit", "Malignant haemangiopericytoma of orbit", "Malignant Hemangiopericytoma of the Orbit", "Malignant hemangiopericytoma of orbit (disorder)", "malignant hemangiopericytoma of orbit (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant hemangiopericytoma of orbit", "shortest_name_length": 34}
{"curie": "UMLS:C0751596", "names": ["Neonatal Pyruvate Dehydrogenase Complex Deficiency Disease", "Pyruvate Dehydrogenase Complex Deficiency Disease, Neonatal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pyruvate Dehydrogenase Complex Deficiency Disease, Neonatal", "shortest_name_length": 58}
{"curie": "MONDO:0021836", "names": ["aksu von stockhausen syndrome", "Aksu von Stockhausen syndrome", "hereditary branchial arch defects", "Hereditary branchial arch defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aksu von Stockhausen syndrome", "shortest_name_length": 29}
{"curie": "UMLS:C4724833", "names": ["Recurrent Thymic Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Thymic Carcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0007795", "names": ["limb uterus syndrome", "LIMB-UTERUS SYNDROME", "Limb uterus syndrome", "Limb-Uterus Syndrome", "limb-uterus syndrome", "hypomelia mullerian duct anomalies", "Hypomelia mullerian duct anomalies", "HYPOMELIA WITH MULLERIAN DUCT ANOMALIES", "Hypomelia with Mullerian Duct Anomalies", "hypomelia with mullerian duct anomalies", "mullerian duct anomalies-limb anomalies syndrome", "Müllerian duct anomalies-limb anomalies syndrome", "Severe upper limb hypoplasia and Mullerian duct anomalies", "severe upper limb hypoplasia and Mullerian duct anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mullerian duct anomalies-limb anomalies syndrome", "shortest_name_length": 20}
{"curie": "UMLS:C1368999", "names": ["LE", "Late effect", "Aftereffect", "late effects", "Late effect of", "Late Adverse Effect", "Adverse Late Effects", "Late Adverse Reaction", "Late effect of medical intervention"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Late effect of medical intervention", "shortest_name_length": 2}
{"curie": "MONDO:0003801", "names": ["corneal intraepithelial neoplasm", "cornea intraepithelial neoplasia", "Cornea Intraepithelial Neoplasia", "Corneal intraepithelial neoplasia", "Corneal Intraepithelial Neoplasia", "corneal intraepithelial neoplasia", "Intraepithelial Neoplasia of Cornea", "intraepithelial neoplasia of cornea", "Intraepithelial Neoplasia of the Cornea", "CIN - corneal intraepithelial neoplasia", "intraepithelial neoplasia of the cornea", "Corneal Squamous Intraepithelial Neoplasia", "Corneal intraepithelial neoplasia (disorder)", "corneal intraepithelial neoplasia (diagnosis)", "cornea squamous cell intraepithelial neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal intraepithelial neoplasm", "shortest_name_length": 32}
{"curie": "UMLS:C1334783", "names": ["testicular embryonal carcinoma and yolk sac tumor with seminoma", "testicular yolk sac tumor with seminoma and embryonal carcinoma", "embryonal carcinoma and yolk sac tumor with seminoma, testicular", "yolk sac tumor with seminoma and embryonal carcinoma of the testis", "testis cancer, yolk sac tumor with seminoma and embryonal carcinoma", "testis cancer, embryonal carcinoma and yolk sac tumor with seminoma", "Mixed Embryonal Carcinoma and Yolk Sac Tumor with Seminoma of Testis", "Testicular Mixed Embryonal Carcinoma and Yolk Sac Tumor with Seminoma", "testicle cancer, yolk sac tumor with seminoma and embryonal carcinoma", "testicular cancer, yolk sac tumor with seminoma and embryonal carcinoma", "Mixed Embryonal Carcinoma and Yolk Sac Neoplasm with Seminoma of Testis", "testicular cancer, embryonal carcinoma and yolk sac tumor with seminoma", "Mixed Embryonal Carcinoma and Yolk Sac Tumor with Seminoma of the Testis", "Testicular Mixed Embryonal Carcinoma and Yolk Sac Neoplasm with Seminoma", "Mixed Embryonal Carcinoma and Yolk Sac Neoplasm with Seminoma of the Testis", "Mixed Embryonal Carcinoma and Endodermal Sinus Tumor with Seminoma of Testis", "Testicular Mixed Embryonal Carcinoma and Endodermal Sinus Tumor with Seminoma", "Mixed Embryonal Carcinoma and Endodermal Sinus Neoplasm with Seminoma of Testis", "Mixed Embryonal Carcinoma and Endodermal Sinus Tumor with Seminoma of the Testis", "Mixed Embryonal Carcinoma and Endodermal Sinus Neoplasm with Seminoma of the Testis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular Mixed Embryonal Carcinoma and Yolk Sac Tumor with Seminoma", "shortest_name_length": 63}
{"curie": "MONDO:0010864", "names": ["T1D7", "IDDM7", "type 1 diabetes mellitus 7", "TYPE 1 DIABETES MELLITUS 7", "INSULIN-DEPENDENT DIABETES MELLITUS 7", "Insulin-Dependent Diabetes Mellitus 7", "insulin-dependent diabetes mellitus 7", "DIABETES MELLITUS, INSULIN-DEPENDENT, 7", "Diabetes Mellitus, Insulin-Dependent, 7", "diabetes mellitus, insulin-dependent, 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type 1 diabetes mellitus 7", "shortest_name_length": 4}
{"curie": "UMLS:C0157461", "names": ["ARF after childbirth", "Postpartum acute renal failure", "Postpartum Acute Renal Failure", "Postpartum acute kidney failure", "acute renal failure after childbirth", "Postpartum acute renal failure (disorder)", "Acute renal failure following labor and delivery", "acute renal failure after childbirth (diagnosis)", "Acute renal failure following labour and delivery", "kidney; insufficiency, following delivery (acute)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postpartum acute renal failure", "shortest_name_length": 20}
{"curie": "UMLS:C3178803", "names": ["Social Anhedonia", "Social Anhedonias", "Anhedonia, Social", "Anhedonias, Social"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Social Anhedonia", "shortest_name_length": 16}
{"curie": "MONDO:0012719", "names": ["PSAPD", "Prosaposin Deficiency", "prosaposin deficiency", "PROSAPOSIN DEFICIENCY", "combined Sap deficiency", "COMBINED SAP DEFICIENCY", "combined SAP deficiency", "combined PSAP deficiency", "Combined Saposin Deficiency", "combined saposin deficiency", "COMBINED SAPOSIN DEFICIENCY", "Combined prosaposin deficiency", "combined prosaposin deficiency", "Encephalopathy due to prosaposin deficiency", "encephalopathy due to prosaposin deficiency", "Encephalopathy due to prosaposin deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined PSAP deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C3873567", "names": ["CIPN", "Peripheral neuropathy due to chemotherapy", "neuropathy peripheral due to chemotherapy", "Chemotherapy-Induced Peripheral Neuropathy", "Chemotherapy induced peripheral neuropathy", "CIPN - Chemotherapy-induced peripheral neuropathy", "Peripheral neuropathy due to chemotherapy (diagnosis)", "Chemotherapeutic Drug - Induced Peripheral Neuropathy", "Peripheral neuropathy due to and following chemotherapy", "Peripheral neuropathy due to and following antineoplastic therapy", "Peripheral neuropathy due to and following antineoplastic therapy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peripheral neuropathy due to and following antineoplastic therapy", "shortest_name_length": 4}
{"curie": "UMLS:C4525726", "names": ["Nuclear Cataract Grade 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nuclear Cataract Grade 4", "shortest_name_length": 24}
{"curie": "UMLS:C0677692", "names": ["Stage II Mantle Cell Lymphoma", "contiguous mantle cell lymphoma stage II", "stage II contiguous mantle cell lymphoma", "Stage II Contiguous Mantle Cell Lymphoma", "Contiguous Mantle Cell Lymphoma Stage II", "Contiguous Stage II Mantle Cell Lymphoma", "contiguous stage II mantle cell lymphoma", "Ann Arbor Stage II Contiguous Mantle Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage II Contiguous Mantle Cell Lymphoma", "shortest_name_length": 29}
{"curie": "MONDO:0013899", "names": ["WMS3", "WEILL-MARCHESANI SYNDROME 3", "Weill-Marchesani syndrome 3", "LTBP2 Weill-Marchesani syndrome", "Weill-Marchesani syndrome type 3", "Weill-Marchesani syndrome 3, recessive", "Weill-Marchesani syndrome caused by mutation in LTBP2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Weill-Marchesani syndrome 3", "shortest_name_length": 4}
{"curie": "MONDO:0016850", "names": ["atypical Norrie disease due to del(X)(p11.3)", "Atypical Norrie disease due to del(X)(p11.3)", "Atypical Norrie disease due to monosomy Xp11.3", "atypical Norrie disease due to monosomy Xp11.3", "Atypical Norrie disease due to nullisomy Xp11.3", "Atypical Norrie disease due to Xp11.3 microdeletion", "atypical Norrie disease due to Xp11.3 microdeletion", "Atypical Norrie disease due to monosomy Xp11.3 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical Norrie disease due to monosomy Xp11.3", "shortest_name_length": 44}
{"curie": "MONDO:0016630", "names": ["isolated dense-SPD", "isolated delta-SPD", "isolated dense-storage pool disease", "isolated delta-storage pool disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated delta-storage pool disease", "shortest_name_length": 18}
{"curie": "MONDO:0005365", "names": ["Surdity", "DEAFNESS", "Deafness", "deafness", "hear loss", "Hypacusis", "hard hear", "hypoacusis", "hypoacuses", "Hypoacusis", "Hypoacuses", "No hearing", "ear deafness", "Hearing loss", "Hearing Loss", "Deafness NOS", "loss hearing", "hearing loss", "hard hearing", "HEARING LOSS", "Loss, Hearing", "loss, hearing", "loss; hearing", "hearing; loss", "Deafness, NOS", "Hearing defect", "DEAFNESS (NOS)", "hearing losses", "Hearing losses", "hard of hearing", "Hearing deficit", "Hearing reduced", "Hard of hearing", "hearing; defect", "deafness degree", "Loss of hearing", "loss of hearing", "HEARING REDUCED", "defect; hearing", "reduced hearing", "hearing impaired", "HEARING IMPAIRED", "Partial deafness", "impaired hearing", "Impaired hearing", "Hearing impaired", "Hearing deficits", "HL - Hearing loss", "decreased hearing", "Hearing defect(s)", "Hearing loss, NOS", "Hearing decreased", "Decreased hearing", "Deafness, partial", "Loss (of);hearing", "HEARING DECREASED", "Hearing impairment", "HEARING IMPAIRMENT", "Hearing Impairment", "difficulty hearing", "Impairment;hearing", "hearing impairment", "Difficulty hearing", "Deafness;congenital", "hearing impairments", "Congenital deafness", "Deafness congenital", "congenital deafness", "DEAFNESS CONGENITAL", "hereditary deafness", "Hereditary deafness", "DEAFNESS, HEREDITARY", "partial hearing loss", "congenital; deafness", "Deafness, congenital", "Unspecified deafness", "deafness (diagnosis)", "deafness; congenital", "Partial Hearing Loss", "Partial hearing loss", "hearing loss disorder", "Hearing Loss, Partial", "HOH - Hard of hearing", "CONGENITAL HEARING LOSS", "Hearing loss (disorder)", "congenital hearing loss", "HI - Hearing impairment", "HEARING LOSS CONGENITAL", "Congenital hearing loss", "Congenital deafness NOS", "Hearing loss, congenital", "Unspecified hearing loss", "hearing loss (diagnosis)", "Deafness all degrees NOS", "Hearing loss, unspecified", "loss of hearing (symptom)", "Decreased hearing (finding)", "Partial deafness (disorder)", "Congenital deafness (disorder)", "congenital deafness (diagnosis)", "Congenital sensorineural deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss disorder", "shortest_name_length": 7}
{"curie": "UMLS:C5204617", "names": ["Advanced Endometrial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Endometrial Carcinoma", "shortest_name_length": 30}
{"curie": "UMLS:C0678050", "names": ["Stage I Adrenal Cortex Cancer", "stage I adrenocortical cancer", "Stage I Adrenal Cortex Carcinoma", "Stage I Adrenocortical Carcinoma", "Stage I Carcinoma of Adrenal Cortex", "Stage I Carcinoma of the Adrenal Cortex", "Stage I Adrenal Cortex Carcinoma AJCC v7", "Stage I Adrenal Cortical Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Adrenal Cortex Carcinoma AJCC v7", "shortest_name_length": 29}
{"curie": "UMLS:C5202584", "names": ["Left Ventricular Hypertrophy with Strain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Left Ventricular Hypertrophy with Strain", "shortest_name_length": 40}
{"curie": "UMLS:C0085618", "names": ["Venospasm", "VENOSPASM", "venospasm", "vein; spasm", "spasm; vein", "Venous spasm", "venous spasm", "spasms veins", "Spasm of vein", "spasms venous", "Venospasm (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Venospasm", "shortest_name_length": 9}
{"curie": "MONDO:0013107", "names": ["ATOD7", "atopic dermatitis 7", "dermatitis, ATOPIC, 7", "Dermatitis, Atopic, 7", "dermatitis, atopic, 7", "DERMATITIS, ATOPIC, 7", "atopic dermatitis type 7", "dermatitis, atopic, susceptibility to, 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermatitis, atopic, 7", "shortest_name_length": 5}
{"curie": "UMLS:C4329704", "names": ["Defective Thyroglobulin Transport"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Defective Thyroglobulin Transport", "shortest_name_length": 33}
{"curie": "UMLS:C0856049", "names": ["Peripheral embolism", "Peripheral embolism NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peripheral embolism", "shortest_name_length": 19}
{"curie": "MONDO:0015361", "names": ["AR demyelinating HMSN", "autosomal recessive hereditary demyelinating motor and sensory neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive hereditary demyelinating motor and sensory neuropathy", "shortest_name_length": 21}
{"curie": "MONDO:0002025", "names": ["disease mental", "Mental disease", "Mental Illness", "Mental illness", "MENTAL ILLNESS", "mental disease", "mental illness", "diseases mental", "Mental disorder", "mental disorder", "Mental Disorder", "disorder mental", "Illness, Mental", "mental disorders", "Mental Disorders", "MENTAL DISORDERS", "Mental disorders", "disorder; mental", "Mental Illnesses", "mental; disorder", "Mental illness NOS", "mental dysfunction", "Mental Dysfunction", "psychiatric illness", "Mental disorder NOS", "Psychiatric Illness", "Psychiatric disease", "Psychiatric Disease", "dysfunctions mental", "Psychiatric illness", "illness psychiatric", "Mental disorder, NOS", "Psychiatric disorder", "Psychiatric Diseases", "disorder psychiatric", "Psychiatric Disorder", "psychiatric disorder", "PSYCHIATRIC DISORDER", "Psychiatric Illnesses", "psychiatric disorders", "PSYCHIATRIC DISORDERS", "Psychiatric disorders", "illnesses psychiatric", "Psychiatric Disorders", "psychiatric; disorder", "disorder psychological", "Disorder;psychological", "Mental health disorder", "psychological disorder", "disorder health mental", "mental health disorder", "disorder mental health", "Psychological disorder", "Psychological Disorders", "PSYCHIATRIC NONSPECIFIC", "Psychiatric disorder NOS", "disease of mental health", "mental disorder disorder", "psychological dysfunction", "dysfunctions psychological", "Psychological disorder NOS", "Mental disorder (disorder)", "Unspecified Mental Disorder", "Unspecified mental disorder", "Psychiatric disease or syndrome", "psychiatric disorders (diagnosis)", "Unspecified mental disorder (F99)", "Emotional or mental disease or syndrome", "Mental disorder, not otherwise specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "psychiatric disorder", "shortest_name_length": 14}
{"curie": "MONDO:0011889", "names": ["Cmt2l", "CMT2I", "CMT 2I", "Charcot-Marie-Tooth disease type 2I", "Charcot Marie Tooth disease type 2I", "CHARCOT-MARIE-TOOTH DISEASE, TYPE 2I", "Charcot-Marie-Tooth disease, type 2I", "Charcot-Marie-Tooth disease, Type 2I", "Charcot-Marie-Tooth neuropathy type 2I", "Charcot-Marie-Tooth neuropathy, type 2I", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2I", "Charcot-Marie-Tooth disease, axonal, type 2I", "Charcot-Marie-Tooth disease, axonal, Type 2I", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2I", "Charcot-Marie-Tooth Neuropathy, Axonal, Type 2l", "Charcot-Marie-Tooth disease type 2I (diagnosis)", "autosomal dominant Charcot-Marie-Tooth disease type 2I", "Autosomal dominant Charcot-Marie-Tooth disease type 2I", "Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2l", "Autosomal dominant Charcot-Marie-Tooth disease type 2I (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 2I", "shortest_name_length": 5}
{"curie": "UMLS:C1336959", "names": ["Very Low Risk Gastric Gastrointestinal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Very Low Risk Gastric Gastrointestinal Stromal Tumor", "shortest_name_length": 52}
{"curie": "UMLS:C1320547", "names": ["Allergic otitis externa", "Allergic otitis externa (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Allergic otitis externa", "shortest_name_length": 23}
{"curie": "UMLS:C3160909", "names": ["Autoimmune arthritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Autoimmune arthritis", "shortest_name_length": 20}
{"curie": "MONDO:0010745", "names": ["XLTT", "GATA1-related X-linked cytopenia", "X-linked thrombocytopenia with beta-thalassemia", "X-linked thrombocytopenia with Beta-thalassemia", "X-Linked Thrombocytopenia with Beta-Thalassemia", "Thrombocytopenia with Beta-Thalassemia, X-Linked", "THROMBOCYTOPENIA WITH BETA-THALASSEMIA, X-LINKED", "thrombocytopenia with BETA-thalassemia, X-linked", "beta-thalassemia-X-linked thrombocytopenia syndrome", "Beta-thalassemia-X-linked thrombocytopenia syndrome", "Beta thalassemia X-linked thrombocytopenia syndrome", "Beta thalassaemia X-linked thrombocytopenia syndrome", "Beta thalassemia X-linked thrombocytopenia syndrome (disorder)", "thrombocytopenia with beta-thalassemia, X-linked, X-linked recessive", "thrombocytopenia, Platelet dysfunction, hemolysis, and Imbalanced globin synthesis", "THROMBOCYTOPENIA, PLATELET DYSFUNCTION, HEMOLYSIS, AND IMBALANCED GLOBIN SYNTHESIS", "Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis", "thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "beta-thalassemia-X-linked thrombocytopenia syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0394003", "names": ["Dystonic/rigid cerebral palsy", "Dystonic-Rigid Cerebral Palsy", "Cerebral Palsy, Dystonic-Rigid", "Cerebral Palsy, Dystonic Rigid", "Dystonic-Rigid Cerebral Palsies", "Cerebral Palsies, Dystonic-Rigid", "Dystonic/rigid cerebral palsy (disorder)", "Dystonic cerebral palsy with spastic features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebral Palsy, Dystonic-Rigid", "shortest_name_length": 29}
{"curie": "MONDO:0017179", "names": ["limbic encephalitis with caspr2 antibodies", "Limbic encephalitis with caspr2 antibodies", "encephalitis limbic with contactin-associated protein-like 2 antibodies", "Limbic encephalitis with contactin-associated protein-like 2 antibodies", "Limbic encephalitis with contactin-associated protein-like 2 antibodies (disorder)", "Limbic encephalitis with contactin-associated protein-like 2 antibodies (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "limbic encephalitis with caspr2 antibodies", "shortest_name_length": 42}
{"curie": "UMLS:C5420025", "names": ["Sinonasal Lymphoepithelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Lymphoepithelial Carcinoma", "shortest_name_length": 36}
{"curie": "UMLS:C4744861", "names": ["Metastatic Digestive System Neuroendocrine Neoplasm", "Metastatic Gastroenteropancreatic Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Digestive System Neuroendocrine Neoplasm", "shortest_name_length": 51}
{"curie": "UMLS:C4684878", "names": ["Advanced Microsatellite Stable Colorectal Cancer", "Advanced Microsatellite Stable Colorectal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Microsatellite Stable Colorectal Carcinoma", "shortest_name_length": 48}
{"curie": "UMLS:C3273018", "names": ["LGDN", "Low Grade Liver Dysplastic Nodule", "Low Grade Hepatic Dysplastic Nodule"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Grade Liver Dysplastic Nodule", "shortest_name_length": 4}
{"curie": "UMLS:C0339546", "names": ["pigment epithelial detachment", "detachment epithelial pigment", "Pigment epithelial detachment", "epithelial pigment detachment", "PED - Pigment epithelial detachment", "Retinal Pigment Epithelial Detachment", "Retinal pigment epithelial detachment", "RPE - Retinal pigment epithelial detachment", "RPED - Retinal pigment epithelial detachment", "Retinal pigment epithelial detachment (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retinal Pigment Epithelial Detachment", "shortest_name_length": 29}
{"curie": "MONDO:0014050", "names": ["MCOP8", "isolated microphthalmia 8", "microphthalmia, isolated 8", "MICROPHTHALMIA, ISOLATED 8", "isolated microphthalmia type 8", "ALDH1A3 isolated microphthalmia", "microphthalmia, isolated type 8", "isolated microphthalmia caused by mutation in ALDH1A3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated microphthalmia 8", "shortest_name_length": 5}
{"curie": "MONDO:0001190", "names": ["Brucella suis brucellosis", "Brucella suis infectious disease", "Brucella suis disease or disorder", "Brucella suis caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brucella suis brucellosis", "shortest_name_length": 25}
{"curie": "UMLS:C0751111", "names": ["Awakening Epilepsy", "Epilepsy, Awakening"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Awakening Epilepsy", "shortest_name_length": 18}
{"curie": "UMLS:C0280178", "names": ["Stage IV Lymphoblastic Lymphoma", "Stage IV Adult Lymphoblastic Lymphoma", "Adult Lymphoblastic Lymphoma Stage IV", "stage IV adult lymphoblastic lymphoma", "Adult Stage IV Lymphoblastic Lymphoma", "adult lymphoblastic lymphoma, stage IV", "metastatic adult lymphoblastic lymphoma", "adult lymphoblastic lymphoma, metastatic", "Stage IV Adult Precursor Lymphoblastic Lymphoma", "Ann Arbor Stage IV Adult Lymphoblastic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Adult Lymphoblastic Lymphoma", "shortest_name_length": 31}
{"curie": "UMLS:C0019319", "names": ["hernia scrotal", "Scrotal Hernia", "Scrotal hernia", "scrotal hernia", "hernia scrotum", "SCROTUM HERNIA", "scrotum hernia", "hernias scrotum", "Hernia, scrotal", "abdomen hernia scrotal", "Scrotal hernia (disorder)", "scrotal hernia (diagnosis)", "scrotal hernia (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Scrotal hernia", "shortest_name_length": 14}
{"curie": "UMLS:C5557268", "names": ["Locally Advanced HER2-Positive Breast Carcinoma", "Locally Advanced HER2 Positive Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced HER2-Positive Breast Carcinoma", "shortest_name_length": 47}
{"curie": "UMLS:C1336916", "names": ["Endometrial Endometrioid Adenocarcinoma with an Undifferentiated Carcinomatous Component"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endometrial Endometrioid Adenocarcinoma with an Undifferentiated Carcinomatous Component", "shortest_name_length": 88}
{"curie": "MONDO:0020547", "names": ["CGVHD", "Chronic", "chronic GVHD", "Chronic GVHD", "GVHD, chronic", "Chronic GVH disease", "chronic graft-versus-host disease", "Chronic graft-versus-host disease", "chronic graft versus host disease", "Chronic Graft Versus Host Disease", "Chronic graft versus host disease", "Graft versus host disease, chronic", "graft versus host disease, chronic", "Chronic graft-versus-host disease (disorder)", "chronic graft-versus-host disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic graft versus host disease", "shortest_name_length": 5}
{"curie": "UMLS:C4525299", "names": ["Stage II Gallbladder Cancer", "Stage II Gallbladder Cancer AJCC v8", "Stage II Gallbladder Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Gallbladder Cancer AJCC v8", "shortest_name_length": 27}
{"curie": "MONDO:0016442", "names": ["elastoma", "Elastoma", "Elastic nevus", "Elastic naevus", "Nevus elasticus", "nevus elasticus", "Naevus elasticus", "pseudoxanthoma elasticum", "elasticum pseudoxanthoma", "Weidman juvenile elastoma", "Nevus elasticus (disorder)", "juvenile elastoma without osteopoikilosis", "Juvenile elastoma without osteopoikilosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "elastoma", "shortest_name_length": 8}
{"curie": "MONDO:0010245", "names": ["COD2", "CORDX2", "cone dystrophy X-linked 2", "X-linked cone dystrophy 2", "CONE DYSTROPHY 2, X-LINKED", "cone dystrophy 2, X-linked", "Cone Dystrophy, X-Linked, 2", "cone-rod dystrophy X-linked 2", "X-linked cone-rod dystrophy 2", "Cone-Rod Dystrophy, X-Linked, 2", "CONE-ROD DYSTROPHY, X-LINKED, 2", "cone-rod dystrophy, X-linked, 2", "X-linked cone-rod dystrophy type 2", "cone dystrophy, progressive X-linked, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked cone-rod dystrophy 2", "shortest_name_length": 4}
{"curie": "MONDO:0020436", "names": ["sinus venosus ASD", "Sinus venosus defect", "defect; sinus venosus", "sinus venosus; defect", "ASD, sinus venosus type", "Sinus venosus defect, NOS", "atrial septal defect sinus venosus", "Sinus venosus atrial septal defect", "sinus venosus atrial septal defect", "Atrial Septal Defect Sinus Venosus", "atrial defect septal sinus venosus", "sinus venosus atrial septal defects", "atrial septal defect, sinus venosus", "atrial septal defect, sinus venosus type", "Atrial septal defect, sinus venosus type", "Sinus venosus atrial septal defect (disorder)", "sinus venosus atrial septal defect (diagnosis)", "Sinus venosus atrial septal defect, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial septal defect, sinus venosus type", "shortest_name_length": 17}
{"curie": "MONDO:0003603", "names": ["Nonsecretory pituitary tumor", "Nonsecretory pituitary tumour", "Nonfunctioning pituitary tumor", "Functionless pituitary neoplasm", "non-functioning pituitary tumor", "Nonfunctioning pituitary tumour", "non-functioning pituitary neoplasm", "non-functioning tumor of pituitary", "non-functioning pituitary gland tumor", "non-functioning neoplasm of pituitary", "non-functioning tumor of the pituitary", "nonfunctional pituitary gland neoplasm", "non-functioning tumor of pituitary gland", "non-functioning pituitary gland neoplasm", "Non-Functioning Pituitary Gland Neoplasm", "non-functioning neoplasm of the pituitary", "Functionless pituitary neoplasm (disorder)", "non-functioning neoplasm of pituitary gland", "non-functioning tumor of the pituitary gland", "non-functioning neoplasm of the pituitary gland", "pituitary gland non-functioning endocrine neoplasm", "non-functioning endocrine neoplasm of pituitary gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-functioning pituitary gland neoplasm", "shortest_name_length": 28}
{"curie": "MONDO:0014270", "names": ["CDG1W", "CDG Iw", "CDG-Iw", "CDG1WAR", "STT3A-CDG", "CDG syndrome type Iw", "congenital disorder of glycosylation Iw", "congenital disorder of glycosylation 1w", "STT3A-congenital disorder of glycosylation", "congenital disorder of glycosylation type Iw", "Congenital disorder of glycosylation type 1w", "congenital disorder of glycosylation type 1w", "Congenital disorder of glycosylation type Iw", "congenital disorder of glycosylation, type Iw", "STT3A-CDG (congenital disorder of glycosylation)", "Congenital disorder of glycosylation type 1w (disorder)", "Congenital disorder of glycosylation type 1w (diagnosis)", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw, AUTOSOMAL RECESSIVE", "congenital disorder of glycosylation, type Iw, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "STT3A-congenital disorder of glycosylation", "shortest_name_length": 5}
{"curie": "UMLS:C1336358", "names": ["Paranasal Sinus Cancer Stage IVA", "Stage IVA Paranasal Sinus Cancer", "Stage IVA Accessory Sinus Carcinoma", "Stage IVA Paranasal Sinus Carcinoma", "Stage IVA Carcinoma of Accessory Sinus", "Stage IVA Carcinoma of Paranasal Sinus", "Stage IVA Paranasal Sinus Cancer AJCC v7", "Stage IVA Carcinoma of the Accessory Sinus", "Stage IVA Carcinoma of the Paranasal Sinus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Paranasal Sinus Cancer AJCC v7", "shortest_name_length": 32}
{"curie": "UMLS:C5670419", "names": ["Locally Advanced Unresectable HER2-Positive Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Unresectable HER2-Positive Breast Carcinoma", "shortest_name_length": 60}
{"curie": "MONDO:0012775", "names": ["THC4", "Thrombocytopenia 4", "THROMBOCYTOPENIA 4", "thrombocytopenia 4", "CYCS thrombocytopenia", "thrombocytopenia type 4", "thrombocytopenia, autosomal dominant, 4", "Thrombocytopenia, Autosomal Dominant, 4", "THROMBOCYTOPENIA, AUTOSOMAL DOMINANT, 4", "thrombocytopenia caused by mutation in CYCS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombocytopenia 4", "shortest_name_length": 4}
{"curie": "MONDO:0016458", "names": ["Dup(8)(q12)", "dup(8)(q12)", "trisomy 8q12", "Trisomy 8q12", "8q12 microduplication syndrome", "8q12 microduplication syndrome (disorder)", "chromosome 8q12 microduplication syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "8q12 microduplication syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0016098", "names": ["NAM", "IMNM", "Anti-SRP myopathy", "anti-SRP myopathy", "Anti-HMG-CoA myopathy", "anti-HMG-CoA myopathy", "Autoimmune necrotizing myopathy", "autoimmune necrotizing myositis", "necrotizing autoimmune myopathy", "Autoimmune necrotising myopathy", "Autoimmune necrotizing myositis", "Immune-mediated necrotising myopathy", "immune-mediated necrotizing myopathy", "Immune mediated necrotizing myopathy", "Immune mediated necrotising myopathy", "Immune-mediated necrotizing myopathy", "Immune myopathy with myocyte necrosis", "immune myopathy with myocyte necrosis", "Autoimmune necrotizing myopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immune-mediated necrotizing myopathy", "shortest_name_length": 3}
{"curie": "UMLS:C0340630", "names": ["AORTA THORACOABDOMINAL ANEURYSM", "Thoracoabdominal aortic aneurysm", "Thoracoabdominal Aortic Aneurysm", "Aneurysm, Thoracoabdominal Aortic", "Aortic Aneurysm, Thoracoabdominal", "aorta; thoracoabdominal, aneurysm", "aneurysm; aorta, thoracoabdominal", "aorta; aneurysm, thoracoabdominal", "Thoracoabdominal Aortic Aneurysms", "thoracoabdominal; aortic, aneurysm", "aneurysm of thoracoabdominal aorta", "TAA Thoracoabdominal Aortic Aneurysm", "Thoracoabdominal aortic aneurysm (disorder)", "aneurysm of thoracoabdominal aorta (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aortic Aneurysm, Thoracoabdominal", "shortest_name_length": 31}
{"curie": "MONDO:0032739", "names": ["SPGF36", "spermatogenic failure 36", "SPERMATOGENIC FAILURE 36"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 36", "shortest_name_length": 6}
{"curie": "MONDO:0007177", "names": ["Auriculoosteodysplasia", "auriculoosteodysplasia", "AURICULOOSTEODYSPLASIA", "Auriculo-osteodysplasia", "auriculo-osteodysplasia", "Multiple osseous dysplasia, characteristic ear shape, and short stature", "multiple osseous dysplasia, characteristic ear shape, and short stature"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "auriculoosteodysplasia", "shortest_name_length": 22}
{"curie": "MONDO:0012151", "names": ["ADHD3", "ATTENTION DEFICIT-HYPERACTIVITY DISORDER, SUSCEPTIBILITY TO, 3", "attention deficit-hyperactivity disorder, susceptibility to, 3", "attention Deficit-hyperactivity disorder, susceptibility to, type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "attention deficit-hyperactivity disorder, susceptibility to, 3", "shortest_name_length": 5}
{"curie": "MONDO:0006002", "names": ["urogenital tuberculosis", "Urogenital tuberculosis", "Urogenital Tuberculoses", "Urogenital Tuberculosis", "tuberculosis urogenital", "Tuberculosis, Urogenital", "Tuberculoses, Urogenital", "tuberculosis genitourinary", "genitourinary; tuberculous", "Genitourinary tuberculosis", "genitourinary tuberculosis", "tuberculosis; genitourinary", "TB - Urogenital tuberculosis", "Tuberculosis genitourinary NOS", "genitourinary system tuberculosis", "Tuberculosis of genitourinary system", "genitourinary tuberculosis (diagnosis)", "Genitourinary tuberculosis, unspecified", "Tuberculosis of genitourinary system, NOS", "Tuberculosis of genitourinary system (disorder)", "Tuberculosis of genitourinary system, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urogenital tuberculosis", "shortest_name_length": 23}
{"curie": "UMLS:C1334985", "names": ["Non-Keratinizing Primary Intraosseous Squamous Cell Carcinoma -Solid Type", "Non-Keratinizing Primary Intraosseous Squamous Cell Carcinoma Arising de novo"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Keratinizing Primary Intraosseous Squamous Cell Carcinoma -Solid Type", "shortest_name_length": 73}
{"curie": "UMLS:C1328543", "names": ["Post procedural inflammation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post procedural inflammation", "shortest_name_length": 28}
{"curie": "UMLS:C1611157", "names": ["Hepatic infiltration eosinophilic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatic infiltration eosinophilic", "shortest_name_length": 33}
{"curie": "UMLS:C0333896", "names": ["Koilocytosis", "koilocytosis", "Koilocytosis, NOS", "Koilocytotic atypia", "Koilocytotic Atypia", "koilocytotic atypia", "Atypia, koilocytotic", "Koilocytotic atypia, NOS", "Koilocytotic atypia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Koilocytotic atypia", "shortest_name_length": 12}
{"curie": "MONDO:0011899", "names": ["NSLH", "NSLH1", "NS/LAH", "Tosti syndrome", "Mazzanti syndrome", "Noonan-Like Syndrome With Loose Anagen Hair", "Noonan-like syndrome with loose anagen hair", "Noonan syndrome-like disorder with loose anagen hair", "Noonan Syndrome-Like Disorder with Loose Anagen Hair", "Noonan syndrome-like disorder with loose anagen hair 1", "Noonan syndrome-like disorder with loose anagen hair (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Noonan syndrome-like disorder with loose anagen hair", "shortest_name_length": 4}
{"curie": "UMLS:C1141926", "names": ["sepsis abdominal", "Abdominal sepsis", "abdominal sepsis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abdominal sepsis", "shortest_name_length": 16}
{"curie": "MONDO:0030727", "names": ["DEE101", "early infantile epileptic encephalopathy 101", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 101", "developmental and epileptic encephalopathy 101"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy 101", "shortest_name_length": 6}
{"curie": "UMLS:C4763390", "names": ["PVRL DLBCL", "PVRL Diffuse Large B-Cell Lymphoma", "Primary Vitreoretinal Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Vitreoretinal Diffuse Large B-Cell Lymphoma", "shortest_name_length": 10}
{"curie": "UMLS:C0265110", "names": ["spasm; cerebral", "cerebral; spasm", "Cerebral Vasospasm", "cerebral vasospasm", "Vasospasm cerebral", "VASOSPASM CEREBRAL", "Vasospasm;cerebral", "Vasospasm, cerebral", "cerebral; vasospasm", "Cerebral Angiospasm", "Vasospasm, Cerebral", "vasospasm; cerebral", "Cerebral Vasospasms", "Angiospasm, Cerebral", "angiospasm; cerebral", "Cerebral Angiospasms", "cerebral; angiospasm", "Vasospasms, Cerebral", "Cerebrovascular spasm", "Cerebral arteriospasm", "Spasm cerebrovascular", "cerebral artery spasm", "Cerebral Artery Spasm", "cerebrovascular spasm", "Cerebrovascular Spasm", "Angiospasms, Cerebral", "Spasm;artery;cerebral", "SPASM CEREBROVASCULAR", "spasm; cerebral artery", "Artery Spasm, Cerebral", "Cerebrovascular Spasms", "Spasm, Cerebrovascular", "Spasm, Cerebral Artery", "Cerebral Artery Spasms", "Artery Spasms, Cerebral", "Spasms, Cerebrovascular", "Cerebral arterial spasm", "Spasms, Cerebral Artery", "artery; spasm, cerebral", "Spasm of cerebral artery", "Spasm of cerebral arteries", "Spasm of cerebral arteries (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebral Vasospasm", "shortest_name_length": 15}
{"curie": "MONDO:0024551", "names": ["XLP", "Xlp", "LYP", "Lyp", "IMD5", "EBVS", "XLP1", "XLPD", "XLP1/SAP", "Duncan disease", "DUNCAN DISEASE", "SAP deficiency", "Purtilo syndrome", "PURTILO SYNDROME", "IMMUNODEFICIENCY 5", "immunodeficiency 5", "Immunodeficiency 5", "SH2D1A deficiency/XLP1", "lymphoproliferative disease, X-linked", "LYMPHOPROLIFERATIVE DISEASE, X-LINKED", "X-linked lymphoproliferative disease 1", "X-linked Lymphoproliferative Syndrome 1", "EBV infection, Severe, susceptibility to", "EBV INFECTION, SEVERE, SUSCEPTIBILITY TO", "lymphoproliferative syndrome, X-linked, 1", "LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1", "SH2D1A/SLAM-associated protein deficiency", "EPSTEIN-BARR VIRUS INFECTION, FAMILIAL FATAL", "X-linked lymphoproliferative syndrome type 1", "Epstein-Barr Virus infection, familial fatal", "INFECTIOUS MONONUCLEOSIS, SEVERE, SUSCEPTIBILITY TO", "infectious mononucleosis, Severe, susceptibility to", "immunodeficiency, X-linked progressive combined variable", "IMMUNODEFICIENCY, X-LINKED PROGRESSIVE COMBINED VARIABLE", "lymphoproliferative syndrome, X-linked, 1, X-linked recessive", "X-linked lymphoproliferative disease due to SH2D1A deficiency", "X-linked lymphoproliferative disease due to SH2D1A deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked lymphoproliferative disease due to SH2D1A deficiency", "shortest_name_length": 3}
{"curie": "MONDO:0017557", "names": ["Madelung deformity, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Madelung deformity, bilateral", "shortest_name_length": 29}
{"curie": "MONDO:0021203", "names": ["SOM", "Serous otitis media", "Serous Otitis Media", "otitis media serous", "media otitis serous", "serous otitis media", "Otitis media serous", "SEROUS OTITIS MEDIA", "Otitis media;serous", "OTITIS MEDIA SEROUS", "OTITIS MEDIA, SEROUS", "Otitis media, serous", "Otitis Media, Serous", "otitis; media, serous", "secretory otitis media", "Serous otitis media NOS", "Otitis media serous NOS", "otitis media with effusion", "Serous otitis media (disorder)", "serous otitis media (diagnosis)", "serous nonsuppurative otitis media"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "serous otitis media", "shortest_name_length": 3}
{"curie": "MONDO:0007098", "names": ["HCHWA", "amyloidosis 6", "Amyloidosis VI", "amyloidosis VI", "ACys amyloidosis", "cystatin amyloidosis", "HCHWA, Icelandic type", "CST3-related amyloidosis", "cerebral amyloid angiopathy", "Hereditary Cerebral Amyloid Angiopathy", "Cerebral Amyloid Angiopathy, Hereditary", "CST3-related cerebral amyloid angiopathy", "hereditary cystatin C amyloid angiopathy", "cerebral amyloid angiopathy, CST3-related", "Hereditary cerebral angiopathic amyloidosis", "Amyloidosis, Cerebroarterial, Icelandic Type", "amyloidosis, Cerebroarterial, Icelandic type", "Autosomal dominant cerebrovascular amyloidosis", "Hereditary cerebral hemorrhage with amyloidosis", "HEREDITARY CEREBRAL HEMORRHAGE WITH AMYLOIDOSIS", "hereditary cerebral hemorrhage with amyloidosis", "Hereditary Cerebral Hemorrhage With Amyloidosis", "Hereditary cerebral haemorrhage with amyloidosis", "cerebral hemorrhage, hereditary, with amyloidosis", "CEREBRAL HEMORRHAGE, HEREDITARY, WITH AMYLOIDOSIS", "Cerebral Hemorrhage, Hereditary, With Amyloidosis", "Hereditary central nervous system amyloid angiopathy", "HCHWA - hereditary cerebral hemorrhage with amyloidosis", "HCHWA - Hereditary cerebral hemorrhage with amyloidosis", "HCHWA - Hereditary cerebral haemorrhage with amyloidosis", "HCHWA - hereditary cerebral haemorrhage with amyloidosis", "Hereditary cerebral hemorrhage with amyloidosis (disorder)", "hereditary cerebral hemorrhage with amyloidosis, Icelandic type", "Hereditary Cerebral Hemorrhage with Amyloidosis, Icelandic Variant", "Cerebral Hemorrhage, Hereditary, with Amyloidosis, Icelandic Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ACys amyloidosis", "shortest_name_length": 5}
{"curie": "UMLS:C5670693", "names": ["Central Nervous System Rosai-Dorfman Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Rosai-Dorfman Disease", "shortest_name_length": 44}
{"curie": "MONDO:0002903", "names": ["Dyslalia", "Misarticulation", "misarticulation", "Deviant phonology", "Abnormal phonology", "Phonology disorder", "disorders phonology", "Phonology Impairment", "Phonology impairment", "Articulatory apraxia", "Phonological disorder", "articulation disorder", "Phonological Disorder", "Articulation disorder", "phonological disorder", "Impairment, Phonology", "Phonology Impairments", "Articulation Disorder", "disorders phonological", "Articulatory dyspraxia", "Impairments, Phonology", "articulation disorders", "Articulation Disorders", "Articulation disorders", "Sound system impairment", "articulation impairment", "Phonological Impairment", "Articulation impairment", "Phonological impairment", "Phonological Impairments", "Disarticulation Disorder", "Impairment, Phonological", "phonological impairments", "Disorder, Disarticulation", "Impairments, Phonological", "Disarticulation Disorders", "Disorders, Disarticulation", "Speech Articulation Disorder", "Speech articulation disorder", "Speech Articulation Disorders", "articulation speech disorders", "Articulation Disorder, Speech", "Articulation Disorders, Speech", "Phonological (speech) disorder", "Phonological disorder (disorder)", "Articulatory dyspraxia (disorder)", "Articulatory dyspraxia (diagnosis)", "Developmental Articulation Disorder", "Developmental phonological disorder", "developmental articulation disorder", "Developmental articulation disorder", "Articulation Disorder, Developmental", "Developmental Articulation Disorders", "Specific speech articulation disorder", "Articulation Disorders, Developmental", "Functional speech articulation disorder", "Developmental speech articulation disorder", "Speech articulation developmental disorder", "developmental disorder - speech articulation", "developmental disorder; speech, articulation", "speech; developmental disorder, articulation", "Developmental articulation disorder (disorder)", "developmental disorder - articulatory dyspraxia", "Developmental articulation disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "articulation disorder", "shortest_name_length": 8}
{"curie": "UMLS:C0473228", "names": ["Ureteric bleeding", "Ureteric Hemorrhage", "Ureteric hemorrhage", "Ureteric haemorrhage", "Hemorrhage from ureter", "Haemorrhage from ureter", "Hemorrhage from ureter (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemorrhage from ureter", "shortest_name_length": 17}
{"curie": "UMLS:C0919644", "names": ["Blast crisis in myelogenous leukemia", "Blast crisis in myelogenous leukaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Blast crisis in myelogenous leukemia", "shortest_name_length": 36}
{"curie": "MONDO:0030705", "names": ["Trichomonal prostatitis", "Trichomonas prostatitis", "Prostatitis trichomonal", "trichomonal prostatitis", "Trichomonas Prostatitis", "Trichomonal prostatitis (disorder)", "trichomonal prostatitis (diagnosis)", "prostatitis; Trichomonas (etiology)", "Trichomonas; prostatitis (etiology)", "prostatitis; Trichomonas (manifestation)", "Trichomonas; prostatitis (manifestation)", "Trichomonas vaginalis prostatitis (disease)", "Trichomonas vaginalis caused prostatitis (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Trichomonas prostatitis", "shortest_name_length": 23}
{"curie": "MONDO:0001709", "names": ["Hypercalcemic Sarcoidosis", "hypercalcemic sarcoidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypercalcemic sarcoidosis", "shortest_name_length": 25}
{"curie": "MONDO:0017427", "names": ["congenital deformities of limbs"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital deformities of limbs", "shortest_name_length": 31}
{"curie": "UMLS:C2981615", "names": ["Stage IV Digestive System Neuroendocrine Tumor", "Stage IV Gastrointestinal Neuroendocrine Neoplasm", "Stage IV Digestive System Neuroendocrine Neoplasm", "Stage IV Digestive System Neuroendocrine Tumor AJCC v7", "Stage IV Digestive System Neuroendocrine Neoplasm AJCC v7", "Stage IV Gastrointestinal Neuroendocrine Neoplasm AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Digestive System Neuroendocrine Tumor AJCC v7", "shortest_name_length": 46}
{"curie": "MONDO:0017341", "names": ["virus associated tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "virus associated tumor", "shortest_name_length": 22}
{"curie": "MONDO:0013747", "names": ["AVSD4", "atrioventricular septal defect 4", "ATRIOVENTRICULAR SEPTAL DEFECT 4", "GATA4 atrioventricular septal defect", "atrioventricular septal defect type 4", "atrioventricular septal defect caused by mutation in GATA4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrioventricular septal defect 4", "shortest_name_length": 5}
{"curie": "MONDO:0003180", "names": ["Adenoid Cystic Skin Carcinoma", "adenoid cystic skin carcinoma", "cutaneous adenocystic carcinoma", "adenoid cystic eccrine carcinoma", "adenoid cystic carcinoma of skin", "Adenoid Cystic Carcinoma of Skin", "Adenoid cystic eccrine carcinoma", "Adenoid Cystic Cutaneous Carcinoma", "adenoid cystic cutaneous carcinoma", "adenoid cystic carcinoma of the skin", "Adenoid Cystic Carcinoma of the Skin", "skin of body adenoid cystic carcinoma", "Primary cutaneous adenocystic carcinoma", "Primary Cutaneous Adenocystic Carcinoma", "primary cutaneous adenocystic carcinoma", "adenoid cystic eccrine carcinoma of skin", "Adenoid cystic eccrine carcinoma of skin", "adenoid cystic carcinoma of skin (diagnosis)", "Adenoid cystic eccrine carcinoma of skin (disorder)", "Primary Adenoid Cystic Carcinoma (PACC) of the Skin", "Adenoid cystic eccrine carcinoma of skin (diagnosis)", "Adenoid cystic eccrine carcinoma (morphologic abnormality)", "adenoid cystic eccrine carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous adenocystic carcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0001695", "names": ["senile ectropion", "Senile ectropion", "Age-related ectropion", "involutional ectropion", "Involutional ectropion", "Senile ectropion (disorder)", "senile ectropion (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "senile ectropion", "shortest_name_length": 16}
{"curie": "MONDO:0004991", "names": ["BAC", "bac", "Alveolar carcinoma", "Alveolar Carcinoma", "alveolar carcinoma", "Carcinoma, Alveolar", "Alveolar Carcinomas", "CARCINOMA, ALVEOLAR", "Carcinomas, Alveolar", "Bronchiolar carcinoma", "Bronchiolar Carcinoma", "bronchiolar carcinoma", "Carcinoma, Bronchiolar", "Bronchiolar Carcinomas", "Alveolar Adenocarcinoma", "alveolar adenocarcinoma", "Alveolar adenocarcinoma", "alveolar cell carcinoma", "Alveolar Cell Carcinoma", "Alveolar cell carcinoma", "ALVEOLAR CELL CARCINOMA", "Carcinomas, Bronchiolar", "Carcinoma, Alveolar Cell", "Adenocarcinoma, Alveolar", "CARCINOMA, ALVEOLAR CELL", "Alveolar Adenocarcinomas", "Alveolar Cell Carcinomas", "Carcinomas, Alveolar Cell", "bronchoalveolar carcinoma", "Adenocarcinomas, Alveolar", "Bronchioalveolar carcinoma", "Bronchiolar adenocarcinoma", "bronchioalveolar carcinoma", "bronchioloalveolar carcinoma", "Bronchioloalveolar Carcinoma", "Bronchioloalveolar carcinoma", "Carcinoma, Bronchioloalveolar", "Bronchioloalveolar Carcinomas", "CARCINOMA, BRONCHIOLOALVEOLAR", "Bronchiolo-alveolar carcinoma", "Bronchiolo-Alveolar Carcinoma", "bronchiolo-alveolar carcinoma", "Carcinoma, Bronchiolo Alveolar", "Bronchiolo-Alveolar Carcinomas", "Terminal bronchiolar carcinoma", "Carcinomas, Bronchioloalveolar", "Carcinoma, Bronchiolo-Alveolar", "bronchoalveolar adenocarcinoma", "Carcinomas, Bronchiolo-Alveolar", "Bronchioalveolar lung carcinoma", "Bronchioalveolar Lung Carcinoma", "bronchioalveolar lung carcinoma", "bronchoalveolar cell lung cancer", "lung cancer, bronchoalveolar cell", "Bronchioloalveolar Adenocarcinoma", "bronchiolo-alveolar lung carcinoma", "Bronchiolo-Alveolar Adenocarcinoma", "Bronchiolo-Alveolar Lung Carcinoma", "bronchiolo-alveolar adenocarcinoma", "Bronchiolo-alveolar adenocarcinoma", "Adenocarcinoma, Bronchiolo-Alveolar", "alveolar adenocarcinoma (diagnosis)", "BRONCHIOLAR ALVEOLAR CELL CARCINOMA", "Bronchiolo-Alveolar Adenocarcinomas", "Adenocarcinoma, Bronchiolo Alveolar", "BRONCHIOLAR-ALVEOLAR CELL CARCINOMA", "Adenocarcinomas, Bronchiolo-Alveolar", "[M]Bronchiolo-alveolar adenocarcinoma", "bronchiolo-alveolar carcinoma of lung", "Bronchiolo-Alveolar Carcinoma of Lung", "Bronchioloalveolar Lung Adenocarcinoma", "bronchioloalveolar lung adenocarcinoma", "minimally invasive lung adenocarcinoma", "Minimally Invasive Lung Adenocarcinoma", "Bronchioalveolar Adenocarcinoma of Lung", "bronchioalveolar adenocarcinoma of lung", "carcinoma, bronchioloalveolar, malignant", "CARCINOMA, BRONCHIOLOALVEOLAR, MALIGNANT", "Bronchioloalveolar Adenocarcinoma of Lung", "Bronchiolo-Alveolar Carcinoma of the Lung", "bronchioloalveolar adenocarcinoma of lung", "bronchiolo-alveolar carcinoma of the lung", "bronchiolo-alveolar adenocarcinoma of lung", "Bronchiolo-alveolar adenocarcinoma of lung", "bronchioalveolar adenocarcinoma of the lung", "Bronchioalveolar Adenocarcinoma of the Lung", "bronchioloalveolar adenocarcinoma of the lung", "Bronchioloalveolar Adenocarcinoma of the Lung", "Alveolar adenocarcinoma (morphologic abnormality)", "bronchiolo-alveolar adenocarcinoma of lung (diagnosis)", "Bronchiolo-alveolar adenocarcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "minimally invasive lung adenocarcinoma", "shortest_name_length": 3}
{"curie": "MONDO:0006861", "names": ["MS", "chloroma", "CHLOROMA", "Chloroma", "Chloromas", "myelosarcoma", "Myelosarcoma", "CANCER, GREEN", "CHLOROMYELOMA", "CHLOROSARCOMA", "CHLOROLEUKEMIA", "Myeloid sarcoma", "myeloid sarcoma", "MYELOID_SARCOMA", "Myeloid Sarcoma", "sarcoma; myeloid", "Sarcoma, Myeloid", "Myeloid Sarcomas", "myeloid; sarcoma", "Sarcomas, Myeloid", "Chloroma (disorder)", "Myeloid sarcoma NOS", "chloroma (diagnosis)", "granulocytic sarcoma", "Granulocytic sarcoma", "Myeloid sarcoma, disease", "leukemia myeloid sarcoma", "Myeloid sarcoma, morphology", "SARCOMA, MYELOID, MALIGNANT", "sarcoma, myeloid, malignant", "myeloid sarcoma (diagnosis)", "Extramedullary myeloid tumor", "extramedullary myeloid tumor", "Extramedullary Myeloid tumor", "Extramedullary Myeloid Tumor", "leukemia myeloid sarcoma chloroma", "Extramedullary Myeloid Cell Tumor", "Myeloid Cell Tumor, Extramedullary", "Myeloid sarcoma, disease (disorder)", "Myeloid sarcoma, morphology (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myeloid sarcoma", "shortest_name_length": 2}
{"curie": "MONDO:0016604", "names": ["Medeira-Dennis-Donnai syndrome", "dysraphism, cleft lip/palate, limb reduction defects", "dysraphism-cleft lip/palate-limb reduction defects syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dysraphism-cleft lip/palate-limb reduction defects syndrome", "shortest_name_length": 30}
{"curie": "UMLS:C4683569", "names": ["Lugano Classification Stage II Adult Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage II Adult Lymphoma AJCC v8", "shortest_name_length": 53}
{"curie": "UMLS:C0234469", "names": ["Global Aphasia", "Global aphasia", "global aphasia", "APHASIA GLOBAL", "aphasia global", "Central aphasia", "Aphasia, Global", "Global Aphasias", "Global dysphasia", "Global Dysphasia", "Cortical aphasia", "global dysphasia", "Global Dysphasias", "Dysphasia, Global", "Pictorial aphasia", "Global aphasia (finding)", "Expressive-receptive aphasia", "Expressive and receptive aphasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aphasia, Global", "shortest_name_length": 14}
{"curie": "UMLS:C0345965", "names": ["Lung Teratoma", "teratoma of lung", "Intrapulmonary teratoma", "teratoma of lung (diagnosis)", "Intrapulmonary teratoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intrapulmonary teratoma", "shortest_name_length": 13}
{"curie": "UMLS:C2983717", "names": ["Penile Cancer by AJCC v6 Stage", "Penile Carcinoma by AJCC v6 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Penile Cancer by AJCC v6 Stage", "shortest_name_length": 30}
{"curie": "MONDO:0021945", "names": ["hear problem", "hear problems", "auditory defect", "problem hearing", "hearing problem", "Hearing problem", "Problem;hearing", "Impaired Hearing", "problem; hearing", "Hearing disorder", "hearing disorder", "auditory effects", "hearing; problem", "Hearing Disorder", "auditory disorder", "Hearing disorders", "hearing disorders", "AUDITORY DISORDER", "disorder; hearing", "Auditory disorder", "disorders hearing", "hearing; disorder", "Hearing Disorders", "auditory disorders", "Auditory Alteration", "disorder of hearing", "Auditory alteration", "Disorder of hearing", "auditory alteration", "of hearing disorder", "auditory disturbance", "Auditory dysfunction", "disturbance; hearing", "Auditory disorder NOS", "auditory disturbances", "AUDITORY DISORDER (NOS)", "Auditory disorder (NOS)", "RNDx auditory alteration", "auditory system disorder", "Hearing problem (finding)", "Disorder of auditory system", "Hearing disorder (disorder)", "Auditory dysfunction (disorder)", "Auditory system disease or syndrome", "RNDx auditory alteration (diagnosis)", "Disorder of auditory system (disorder)", "Sensory perceptual alteration: auditory"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing disorder", "shortest_name_length": 12}
{"curie": "MONDO:0008652", "names": ["CVT", "Convex Foot", "Foot, Convex", "Vertical tali", "Vertical talus", "Rigid Flatfoot", "vertical talus", "Vertical Talus", "Talus, Vertical", "Flatfoot, Rigid", "Convex Pes Valgus", "Convex pes valgus", "Rockerbottom feet", "Rocker bottom foot", "ROCKER-BOTTOM FOOT", "rocker bottom feet", "rocker bottom foot", "Rocker bottom feet", "ROCKER BOTTOM FEET", "Rocker-Bottom Foot", "rocker-bottom foot", "Pes Valgus, Convex", "Rocker Bottom Foot", "Rocker-bottom feet", "Foot, Rocker-Bottom", "'Rocker bottom' feet", "'Rocker-bottom' feet", "congenital convex foot", "Congenital convex foot", "congenital vertical talus", "Congenital Vertical Talus", "Congenital vertical talus", "VERTICAL TALUS, CONGENITAL", "vertical talus, congenital", "Vertical Talus, Congenital", "Talus, Congenital Vertical", "feet pes rocker bottom foot", "congenital convex pes valgus", "Congenital convex pes valgus", "rocker-bottom foot deformity", "pes valgus, congenital convex", "PES VALGUS, CONGENITAL CONVEX", "Congenital rocker-bottom foot", "congenital rocker-bottom foot", "Pes Valgus, Congenital Convex", "CVT - Congenital vertical talus", "CCPV - Congenital convex pes valgus", "Congenital vertical talus (disorder)", "[OBSOLETE] Vertical talus, congenital", "rocker bottom foot (physical finding)", "Charcot-Marie-Tooth disease, foot deformity of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital vertical talus", "shortest_name_length": 3}
{"curie": "UMLS:C0546126", "names": ["Acute Confusional Senile Dementia", "Senile Dementia, Acute Confusional", "Senile dementia, acute confusional"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Confusional Senile Dementia", "shortest_name_length": 33}
{"curie": "MONDO:0004381", "names": ["intraductal pancreatic papillary mucinous adenoma", "pancreatic intraductal papillary-mucinous adenoma", "Pancreatic Intraductal Papillary-Mucinous Adenoma", "Intraductal papillary mucinous adenoma of pancreas", "intraductal papillary-mucinous adenoma of pancreas", "Intraductal papillary mucinous adenoma of pancreas (disorder)", "Pancreatic Intraductal Papillary-Mucinous Neoplasm, Low Grade", "Pancreatic Intraductal Papillary-Mucinous Neoplasm, Low-Grade", "intraductal papillary-mucinous adenoma of pancreas (diagnosis)", "Pancreatic Intraductal Papillary-Mucinous Neoplasm with Low Grade Dysplasia", "pancreatic intraductal papillary-mucinous neoplasm with low grade dysplasia", "Pancreatic Intraductal Papillary Mucinous Neoplasm with Low Grade Dysplasia", "pancreatic intraductal papillary mucinous neoplasm with Low grade dysplasia", "pancreatic intraductal papillary-mucinous neoplasm with Low grade dysplasia", "Intraductal papillary mucinous neoplasm with moderate dysplasia of pancreas", "Intraductal papillary mucinous neoplasm with low grade dysplasia of pancreas", "Intraductal papillary mucinous neoplasm with intermediate dysplasia of pancreas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic intraductal papillary-mucinous neoplasm with low grade dysplasia", "shortest_name_length": 49}
{"curie": "UMLS:C3826890", "names": ["Pancreatic BD-IPMN", "Pancreatic SB-IPMN", "Side Branch Pancreatic Intraductal Papillary-Mucinous Neoplasm", "Branch Duct Pancreatic Intraductal Papillary-Mucinous Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Branch Duct Pancreatic Intraductal Papillary-Mucinous Neoplasm", "shortest_name_length": 18}
{"curie": "MONDO:0016408", "names": ["permanent congenital hypothyroidism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "permanent congenital hypothyroidism", "shortest_name_length": 35}
{"curie": "MONDO:0016468", "names": ["toxin-mediated infective botulism", "toxin-mediated infectious botulism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "toxin-mediated infectious botulism", "shortest_name_length": 33}
{"curie": "MONDO:0017270", "names": ["autosomal ichthyosis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal ichthyosis syndrome", "shortest_name_length": 29}
{"curie": "UMLS:C4727075", "names": ["Refractory Mediastinal Lymphoma", "Refractory Primary Mediastinal Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Mediastinal Lymphoma", "shortest_name_length": 31}
{"curie": "MONDO:0043131", "names": ["Michels Caskey syndrome", "michels caskey syndrome", "Mullerian aplasia with hypoplastic thumbs", "Mullerian aplasia with unilateral hypoplasia of the thumbs and skeletal spine deformities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "michels caskey syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0015509", "names": ["genetic biliary tract disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genetic biliary tract disease", "shortest_name_length": 29}
{"curie": "UMLS:C0265675", "names": ["Scoliosis", "inborn scoliosis", "Scoliosis;congenital", "Congenital scoliosis", "congenital scoliosis", "congenital; scoliosis", "scoliosis; congenital", "Scoliosis, congenital", "Congenital scoliosis NOS", "Congenital Postural Scoliosis", "Congenital postural scoliosis", "congenital; scoliosis, postural", "scoliosis; congenital, postural", "congenital scoliosis (diagnosis)", "inborn lateral curvature of the spine", "Congenital postural scoliosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital postural scoliosis", "shortest_name_length": 9}
{"curie": "UMLS:C3273254", "names": ["Arterionephrosclerosis", "Benign Nephrosclerosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arterionephrosclerosis", "shortest_name_length": 22}
{"curie": "UMLS:C0877077", "names": ["Myocardial bleeding", "Myocardial hemorrhage", "Myocardial haemorrhage", "Myocardial hemorrhage (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myocardial hemorrhage", "shortest_name_length": 19}
{"curie": "UMLS:C1963746", "names": ["Abdominal wall hematoma", "Abdominal wall haematoma", "Hematoma of abdominal wall", "Haematoma of abdominal wall", "Hematoma of abdominal wall (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hematoma of abdominal wall", "shortest_name_length": 23}
{"curie": "MONDO:0001825", "names": ["squamous papilloma", "Squamous Papilloma", "Squamous papilloma", "Keratotic Papilloma", "Keratotic papilloma", "papillomas squamous", "keratotic papilloma", "Keratotoc papilloma", "epidermoid papilloma", "Epidermoid papilloma", "Epidermoid Papilloma", "Dyskeratotic papilloma", "Squamous Cell Papilloma", "Squamous cell papilloma", "Parakeratotic papilloma", "squamous cell papilloma", "Squamous Cell Papillomas", "Papilloma, Squamous Cell", "Hyperkeratotic papilloma", "cells papilloma squamous", "Epidermoid Cell Papilloma", "Papillomas, Squamous Cell", "epidermoid cell papilloma", "Squamous cell papilloma, NOS", "papilloma, squamous cell, benign", "PAPILLOMA, SQUAMOUS CELL, BENIGN", "squamous cell papilloma (morphologic abnormality)", "Squamous cell papilloma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "squamous papilloma", "shortest_name_length": 18}
{"curie": "UMLS:C0919804", "names": ["Liver carcinoma ruptured"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liver carcinoma ruptured", "shortest_name_length": 24}
{"curie": "MONDO:0001019", "names": ["AMBLYOPIA STRABISMIC", "strabismic amblyopia", "amblyopia strabismic", "Amblyopia strabismic", "Strabismic amblyopia", "Suppression Amblyopia", "Amblyopia, strabismic", "Suppression amblyopia", "Amblyopia suppression", "suppression amblyopia", "Suppression Amblyopias", "Amblyopia, suppression", "Amblyopia, Suppression", "Amblyopias, Suppression", "Strabismic amblyopia (disorder)", "strabismic amblyopia (diagnosis)", "Stimulus Deprivation-Induced Amblyopia", "Stimulus Deprivation Induced Amblyopia", "Deprivation-Induced Amblyopia, Stimulus", "Stimulus Deprivation-Induced Amblyopias", "Amblyopia, Stimulus Deprivation-Induced", "Amblyopia, Stimulus Deprivation Induced", "Deprivation-Induced Amblyopias, Stimulus", "Amblyopias, Stimulus Deprivation-Induced"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "suppression amblyopia", "shortest_name_length": 20}
{"curie": "UMLS:C0276141", "names": ["Viral bronchitis", "BRONCHITIS VIRAL", "Bronchitis viral", "virus; bronchitis", "bronchitis; viral", "Viral bronchitis, NOS", "Viral bronchitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Viral bronchitis", "shortest_name_length": 16}
{"curie": "UMLS:C4683234", "names": ["Clinical Stage III Retinoblastoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage III Retinoblastoma AJCC v8", "shortest_name_length": 41}
{"curie": "MONDO:0013652", "names": ["NRCLP7", "NARCOLEPSY 7", "narcolepsy 7", "MOG narcolepsy", "narcolepsy type 7", "narcolepsy caused by mutation in MOG"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "narcolepsy 7", "shortest_name_length": 6}
{"curie": "MONDO:0004442", "names": ["testis polyembryoma", "polyembryoma of testis", "Polyembryoma of Testis", "Polyembryoma of testis", "testicular polyembryoma", "Testicular Polyembryoma", "polyembryoma of the testis", "Polyembryoma of the Testis", "polyembryoma of testis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testis polyembryoma", "shortest_name_length": 19}
{"curie": "MONDO:0022809", "names": ["Colver Steer Godman syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colver Steer Godman syndrome", "shortest_name_length": 28}
{"curie": "UMLS:C0393615", "names": ["Familial tremor", "tremor familial", "FAMILIAL TREMOR", "Familial Tremor", "familial tremor", "Tremor familial", "familial; tremor", "familial tremors", "tremor; familial", "Familial Tremors", "Tremor, Familial", "Tremors, Familial", "tremor; hereditary", "hereditary; tremor", "Heredofamilial tremor", "Benign familial tremor", "benign familial tremor", "benign familial tremors", "TREMOR, HEREDITARY, BENIGN", "Hereditary essential tremor", "Hereditary Essential Tremor", "benign familial tremor (diagnosis)", "Hereditary essential tremor (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Familial Tremor", "shortest_name_length": 15}
{"curie": "MONDO:0015721", "names": ["Mild hemophilia A", "mild hemophilia A", "Mild haemophilia A", "HEMOPHILIA A, MILD", "mild hemophilia type A", "6-60% of normal factor VIII", "mild factor VIII deficiency", "Mild congenital F8 deficiency", "Mild congenital factor VIII deficiency", "Mild hereditary factor VIII deficiency disease", "Mild hereditary factor VIII deficiency disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mild hemophilia A", "shortest_name_length": 17}
{"curie": "MONDO:0004032", "names": ["Ovarian Seromucinous Carcinoma", "ovarian seromucinous carcinoma", "ovarian Seromucinous carcinoma", "Ovarian mixed epithelial carcinoma", "ovarian mixed epithelial carcinoma", "Mixed Epithelial Carcinoma of Ovary", "epithelial carcinoma, ovarian mixed", "mixed epithelial carcinoma of ovary", "mixed ephithelial carcinoma, ovarian", "Mixed Epithelial Carcinoma of the Ovary", "mixed epithelial carcinoma of the ovary", "Malignant Ovarian Mixed Epithelial Tumor", "malignant ovarian mixed epithelial tumor", "Malignant Ovarian Mixed Epithelial Neoplasm", "malignant ovarian mixed epithelial neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian seromucinous carcinoma", "shortest_name_length": 30}
{"curie": "UMLS:C1336413", "names": ["Stage IV Bone Sarcoma", "Stage IV Sarcoma of Bone", "Stage IV Sarcoma of the Bone", "Stage IV Bone Sarcoma AJCC v7", "Stage IV Bone Sarcoma  AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Bone Sarcoma AJCC v7", "shortest_name_length": 21}
{"curie": "MONDO:0027694", "names": ["ALS23", "AMYOTROPHIC LATERAL SCLEROSIS 23", "amyotrophic lateral sclerosis 23", "Amyotrophic Lateral Sclerosis 23", "amyotrophic lateral sclerosis type 23"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyotrophic lateral sclerosis type 23", "shortest_name_length": 5}
{"curie": "MONDO:0007218", "names": ["BDA4", "Brachydactyly type A4", "Type A4 brachydactyly", "brachydactyly type A4", "brachydactyly, type A4", "BRACHYDACTYLY, TYPE A4", "Brachydactyly, type A4", "brachydactyly Temtamy type", "Temtamy type brachydactyly", "Brachydactyly Temtamy type", "Brachymesophalangy 2 and 5", "TEMTAMY TYPE BRACHYDACTYLY", "Brachymesophalangy II and V", "BRACHYMESOPHALANGY II AND V", "Brachymesophalangy II And V", "brachymesophalangy II and V", "Brachydactyly, Temtamy type", "brachydactyly, Temtamy type", "Brachydactyly type A4 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly type A4", "shortest_name_length": 4}
{"curie": "MONDO:0024613", "names": ["Bipolar depression", "bipolar depression", "depression bipolar", "Bipolar Depression", "Depression, Bipolar", "BIPOLAR DISEASE, DEPRESSED", "bipolar disorder depressed", "bipolar disorder depression", "depression bipolar disorder", "bipolar depression disorder", "BIPOLAR DISORDER DEPRESSION", "BIPOLAR DISORDER, DEPRESSED", "CYCLOTHYMIC DISORDER, DEPRESSED", "manic-depressive - now depressed", "Manic-depressive - now depressed", "Bipolar affective disorder, depressed", "MANIC DEPRESSIVE DISEASE DEPRESSED PHASE", "MANIC DEPRESSIVE DISEASE, DEPRESSED PHASE", "bipolar disorder affective, current episode depressed", "bipolar affective disorder, current episode depressed", "bipolar affective disorder, current episode depression", "Bipolar affective disorder, current episode depression", "bipolar affective disorder, current episode depressed (diagnosis)", "Bipolar affective disorder, current episode depression (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bipolar depression", "shortest_name_length": 18}
{"curie": "MONDO:0010699", "names": ["CMTX5", "CMT5X", "ROSENBERG-CHUTORIAN SYNDROME", "Rosenberg-Chutorian Syndrome", "Rosenberg-Chutorian syndrome", "Rosenberg Chutorian syndrome", "Optic atrophy polyneuropathy deafness", "Charcot-Marie-Tooth neuropathy X type 5", "optic atrophy, polyneuropathy, and deafness", "X-linked Charcot-Marie-Tooth disease type 5", "OPTIC ATROPHY, POLYNEUROPATHY, AND DEAFNESS", "Optic atrophy, polyneuropathy, and deafness", "Charcot-Marie-Tooth disease X-linked, 5 (CMTX5)", "Charcot-Marie-Tooth disease X-linked recessive 5", "Charcot-Marie-Tooth disease, X-linked recessive, 5", "Charcot-Marie-Tooth Disease, X-Linked Recessive, 5", "CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 5", "Charcot-Marie-Tooth neuropathy X-linked recessive 5", "Charcot-Marie-Tooth Neuropathy, X-Linked Recessive, 5", "CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED RECESSIVE, 5", "Charcot-Marie-Tooth neuropathy, X-linked recessive, 5", "Charcot-Marie-Tooth disease X-linked recessive type 5", "X-linked Charcot-Marie-Tooth disease type 5 (disorder)", "Charcot-Marie-Tooth disease, X-linked recessive, type 5", "Charcot-Marie-Tooth disease X-linked, 5 (CMTX5) (diagnosis)", "optic atrophy, sensorineural hearing loss and polyneuropathy", "Optic atrophy, sensorineural hearing loss and polyneuropathy", "Familial opticoacoustic nerve degeneration and polyneuropathy", "familial opticoacoustic nerve degeneration and polyneuropathy", "Optic atrophy, neural deafness, and distal neurogenic amyotrophy", "Charcot-Marie-Tooth disease, X-linked recessive, 5, X-linked recessive", "Optic atrophy, hearing loss, and peripheral neuropathy, autosomal recessive", "OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease X-linked recessive 5", "shortest_name_length": 5}
{"curie": "UMLS:C0206646", "names": ["Abdominal desmoid", "abdominal desmoid", "Abdominal Desmoid", "desmoid; abdominal", "abdominal; desmoid", "Mesenteric Desmoid", "Intraabdominal Desmoid", "abdominal fibromatosis", "Abdominal Fibromatosis", "fibromatosis abdominal", "Abdominal Fibromatoses", "Abdominal fibromatosis", "Mesenteric fibromatosis", "mesenteric fibromatosis", "Abdominal Desmoid Tumor", "Abdominal desmoid tumor", "Mesenteric Fibromatosis", "Fibromatoses, Abdominal", "Fibromatosis, Abdominal", "Mesenteric Desmoid Tumor", "Abdominal desmoid tumour", "abdominal; desmoid tumor", "abdominal; tumor, desmoid", "tumor; desmoid, abdominal", "desmoid; tumor, abdominal", "tumor; abdominal, desmoid", "Intraabdominal Fibromatosis", "Retroperitoneal fibromatosis", "Intraabdominal Desmoid Tumor", "retroperitoneal fibromatosis", "retroperitoneal; fibromatosis", "fibromatosis; retroperitoneal", "Peritoneal Desmoid Fibromatosis", "Abdominal fibromatosis (disorder)", "Abdominal fibromatosis (diagnosis)", "Abdominal (Mesenteric) Fibromatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fibromatosis, Abdominal", "shortest_name_length": 17}
{"curie": "UMLS:C4054403", "names": ["Nephropathy due to Cisplatin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephropathy due to Cisplatin", "shortest_name_length": 28}
{"curie": "MONDO:0003948", "names": ["Cerebral Angioma", "cerebral angioma", "Angioma of Cerebrum", "angioma of cerebrum", "cerebral hemangioma", "Cerebral Hemangioma", "Cerebral hemangioma", "cerebral hemangiomas", "Cerebral haemangioma", "Hemangioma of Cerebrum", "hemangioma of cerebrum", "hemangioma of Cerebrum", "angioma of the cerebrum", "Angioma of the Cerebrum", "telencephalon hemangioma", "Hemangioma of the Cerebrum", "hemangioma of the cerebrum", "hemangioma of telencephalon", "Cerebral Hemispheric Angioma", "cerebral hemispheric angioma", "angioma of cerebral hemispheres", "cerebral hemispheric hemangioma", "Angioma of Cerebral Hemispheres", "Cerebral Hemispheric Hemangioma", "hemangioma of cerebral hemispheres", "Hemangioma of Cerebral Hemispheres", "Angioma of the Cerebral Hemispheres", "angioma of the cerebral hemispheres", "hemangioma of the cerebral hemispheres", "Hemangioma of the Cerebral Hemispheres"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral hemangioma", "shortest_name_length": 16}
{"curie": "MONDO:0003468", "names": ["biphasic synovial sarcoma", "Biphasic Synovial Sarcoma", "synovial sarcoma, biphasic", "Synovial sarcoma, biphasic", "Synovial sarcoma - biphasic", "Biphasic Sarcoma of Synovium", "Biphasic sarcoma of Synovium", "biphasic sarcoma of synovium", "Synovial sarcoma, biphasic type", "Biphasic Sarcoma of the Synovium", "biphasic sarcoma of the synovium", "biphasic synovial sarcoma (diagnosis)", "synovial sarcoma, biphasic (morphologic abnormality)", "Synovial sarcoma, biphasic (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "biphasic synovial sarcoma", "shortest_name_length": 25}
{"curie": "UMLS:C0854860", "names": ["Stage I T Lymphoblastic Leukemia/Lymphoma", "Stage I T-Lymphoblastic Leukemia/Lymphoma", "Precursor T-lymphoblastic lymphoma/leukemia stage I", "Stage I Precursor T-Lymphoblastic Lymphoma/Leukemia", "Precursor T-Lymphoblastic Lymphoma/Leukemia Stage I", "Precursor T-lymphoblastic lymphoma/leukaemia stage I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Precursor T-lymphoblastic lymphoma/leukemia stage I", "shortest_name_length": 41}
{"curie": "UMLS:C4331401", "names": ["Temporal Lobe, Parietal Lobe, and Lateral Ventricle Ependymal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Temporal Lobe, Parietal Lobe, and Lateral Ventricle Ependymal Tumor", "shortest_name_length": 67}
{"curie": "UMLS:C0948292", "names": ["IOL dislocation", "Intraocular Lens Dislocation", "Intraocular lens dislocation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IOL dislocation", "shortest_name_length": 15}
{"curie": "UMLS:C0949072", "names": ["Extracorporeal Circuit Clot", "Clotting of extracorporeal circuit"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clotting of extracorporeal circuit", "shortest_name_length": 27}
{"curie": "MONDO:0015503", "names": ["nose and cavum anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nose and cavum anomaly", "shortest_name_length": 22}
{"curie": "MONDO:0007275", "names": ["CTS", "CTS1", "Carpal canal", "Carpal tunnel", "carpal tunnel syndrome", "SYNDROME CARPEL TUNNEL", "CARPAL TUNNEL SYNDROME", "Carpal Tunnel Syndrome", "Carpal tunnel syndrome", "CARPEL TUNNEL SYNDROME", "syndrome; carpal tunnel", "MEDIAN NERVE ENTRAPMENT", "Median nerve entrapment", "carpal tunnel; syndrome", "Carpal Tunnel Syndromes", "Syndrome, Carpal Tunnel", "median nerve entrapment", "MEDIAN NERVE COMPRESSION", "Syndromes, Carpal Tunnel", "Median nerve compression", "CTS - Carpal tunnel syndrome", "CTS - carpal tunnel syndrome", "CTS (carpal tunnel syndrome)", "carpal tunnel syndrome (CTS)", "Constrictive median neuropathy", "Distal median nerve entrapment", "carpal tunnel median neuropathy", "Distal median nerve compression", "Median Neuropathy, Carpal Tunnel", "Carpal tunnel syndrome (disorder)", "carpal tunnel syndrome (diagnosis)", "Amyotrophy, Thenar, Of Carpal Origin", "AMYOTROPHY, THENAR, OF CARPAL ORIGIN", "Entrapment Neuropathy, Carpal Tunnel", "amyotrophy, thenar, of carpal origin", "Compression Neuropathy, Carpal Tunnel", "Carpal tunnel syndrome, unspecified upper limb"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carpal tunnel syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0011892", "names": ["EIG9", "EJM6", "CACNB4 generalised epilepsy", "idiopathic generalized epilepsy 9", "generalised epilepsy caused by mutation in CACNB4", "epilepsy, juvenile myoclonic, susceptibility to, 6", "EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 6", "susceptibility to idiopathic generalized epilepsy 9", "EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 9", "epilepsy, idiopathic generalized, susceptibility to, 9", "EPILEPSY, GENERALIZED IDIOPATHIC, SUSCEPTIBILITY TO, 9", "epilepsy, idiopathic generalized, susceptibility to, type 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, idiopathic generalized, susceptibility to, 9", "shortest_name_length": 4}
{"curie": "UMLS:C1868769", "names": ["Anaphylactoid syndrome of pregnancy", "Anaphylactoid syndrome in pregnancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anaphylactoid syndrome of pregnancy", "shortest_name_length": 35}
{"curie": "UMLS:C5421281", "names": ["Digestive System Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Digestive System Sarcoma", "shortest_name_length": 24}
{"curie": "MONDO:0019256", "names": ["sterol metabolism disorder", "inborn error of sterol metabolic process", "inborn sterol metabolic process disorder", "rare inborn error of sterol metabolic process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sterol metabolism disorder", "shortest_name_length": 26}
{"curie": "MONDO:0010575", "names": ["DHS", "Deafness-hypogonadism syndrome", "DEAFNESS-HYPOGONADISM SYNDROME", "deafness hypogonadism syndrome", "deafness-hypogonadism syndrome", "Deafness-Hypogonadism Syndrome", "Deafness and hypogonadism syndrome", "Hearing loss-hypogonadism syndrome", "Deafness and hypogonadism syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness-hypogonadism syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0014156", "names": ["ATFB14", "atrial fibrillation familial 14", "atrial fibrillation, familial, 14", "ATRIAL FIBRILLATION, FAMILIAL, 14", "SCN2B familial atrial fibrillation", "atrial fibrillation, familial, type 14", "atrial fibrillation familial 14 (diagnosis)", "familial atrial fibrillation caused by mutation in SCN2B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial fibrillation, familial, 14", "shortest_name_length": 6}
{"curie": "UMLS:C0474983", "names": ["tongue hematoma", "TONGUE HEMATOMA", "Tongue hematoma", "hematoma tongue", "Tongue haematoma", "TONGUE HAEMATOMA", "Hematoma of tongue", "Haematoma of tongue", "Hematoma of tongue (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hematoma of tongue", "shortest_name_length": 15}
{"curie": "UMLS:C1334685", "names": ["Medulloblastoma with Leptomeningeal Spread"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Medulloblastoma with Leptomeningeal Spread", "shortest_name_length": 42}
{"curie": "UMLS:C3272531", "names": ["Small Intestinal NEC", "Small Intestinal Neuroendocrine Cancer", "Small Intestinal Neuroendocrine Carcinoma", "Small Intestinal High Grade Neuroendocrine Carcinoma", "Small Intestinal Poorly Differentiated Endocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Intestinal Neuroendocrine Carcinoma", "shortest_name_length": 20}
{"curie": "UMLS:C0855069", "names": ["Rhabdosarcoma recurrent", "Relapsed Rhabdomyosarcoma", "Recurrent Rhabdomyosarcoma", "Rhabdomyosarcoma Recurrent", "Rhabdomyosarcoma recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Rhabdomyosarcoma", "shortest_name_length": 23}
{"curie": "UMLS:C2984534", "names": ["Stage III Gallbladder Cancer", "Gallbladder Cancer Stage III AJCC v6", "Stage III Gallbladder Cancer AJCC v6", "Stage III Gallbladder Carcinoma AJCC v6", "Gallbladder Carcinoma Stage III AJCC v6", "Stage III Carcinoma of Gallbladder AJCC v6", "Stage III Carcinoma of the Gallbladder AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Gallbladder Cancer AJCC v6", "shortest_name_length": 28}
{"curie": "UMLS:C3888500", "names": ["Ulcerated hemangioma", "Ulcerated haemangioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ulcerated hemangioma", "shortest_name_length": 20}
{"curie": "MONDO:0010579", "names": ["CND", "Dermoids of cornea", "dermoids of cornea", "DERMOIDS OF CORNEA", "X-linked corneal dermoid", "Bilateral corneal dermoids", "bilateral corneal dermoids", "corneal dermoids and short stature", "Corneal dermoids and short stature", "X-linked corneal dermoid (disorder)", "Guízar Vázquez-Luengas-Muñoz syndrome", "Guizar-Vazquez Luengas-Munoz syndrome", "Guízar Vázquez-Luengas-muñoz syndrome", "Guízar Vázquez Luengas Muñoz syndrome", "corneal dystrophy epithelial-short stature syndrome", "Corneal dystrophy epithelial-short stature syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked corneal dermoid", "shortest_name_length": 3}
{"curie": "UMLS:C0008298", "names": ["choanal polyp", "Choanal polyp", "polyp; choanal", "choanal; polyp", "Polyp, choanal", "Nasopharynx Polyp", "antrochoanal polyp", "Antrochoanal polyp", "antrochoanal polyps", "Polyp of Nasopharynx", "Nasopharyngeal polyp", "nasopharyngeal polyp", "Nasopharyngeal Polyp", "Polyp in nasopharynx", "nasopharyngeal; polyp", "polyp; nasopharyngeal", "Polyp, nasopharyngeal", "Nasal polyp - posterior", "Choanal polyp (disorder)", "Polyp of the Nasopharynx", "Polyp in nasopharynx (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Choanal polyp", "shortest_name_length": 13}
{"curie": "UMLS:C1096063", "names": ["Refractory epilepsy", "Refractory Epilepsy", "Intractable Epilepsy", "epilepsy intractable", "intractable epilepsy", "Intractable epilepsy", "Epilepsy, refractory", "Epilepsy, Refractory", "Epilepsy, Intractable", "Refractory Epilepsies", "Intractable Epilepsies", "Epilepsies, Refractory", "Drug Resistant Epilepsy", "Epilepsies, Intractable", "Resistant Epilepsy, Drug", "Drug Refractory Epilepsy", "Epilepsy, Drug Resistant", "Drug Resistant Epilepsies", "Epilepsy, Drug Refractory", "Refractory Epilepsy, Drug", "Drug Refractory Epilepsies", "Epilepsies, Drug Resistant", "Resistant Epilepsies, Drug", "Epilepsies, Drug Refractory", "Refractory Epilepsies, Drug", "Medication Resistant Epilepsy", "Refractory epilepsy (disorder)", "Resistant Epilepsy, Medication", "Epilepsy, Medication Resistant", "Medication Resistant Epilepsies", "Resistant Epilepsies, Medication", "Epilepsies, Medication Resistant", "epilepsy intractable (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drug Resistant Epilepsy", "shortest_name_length": 19}
{"curie": "MONDO:0060491", "names": ["NEDIM", "NEURODEVELOPMENTAL DISORDER WITH INVOLUNTARY MOVEMENTS", "neurodevelopmental disorder with involuntary movements"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with involuntary movements", "shortest_name_length": 5}
{"curie": "MONDO:0002227", "names": ["ovary lymphoma", "ovarian lymphoma", "Ovarian Lymphoma", "lymphoma of ovary", "primary ovarian lymphoma", "Primary Ovarian Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian lymphoma", "shortest_name_length": 14}
{"curie": "UMLS:C1565107", "names": ["Secondary Headache Disorder", "Headache Disorder, Secondary", "Disorder, Secondary Headache", "Secondary Headache Disorders", "Headache Disorders, Secondary", "Disorders, Secondary Headache"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Headache Disorders, Secondary", "shortest_name_length": 27}
{"curie": "MONDO:0001713", "names": ["inherited aplastic anemia", "Congenital aplastic anemia", "hereditary aplastic anemia", "congenital aplastic anemia", "congenital aplastic anaemia", "Familial hypoplastic anemia", "familial hypoplastic anemia", "Congenital aplastic anaemia", "aplastic; anemia, congenital", "familial hypoplastic anaemia", "anemia; aplastic, congenital", "Familial hypoplastic anaemia", "hypoplastic anemia - familial", "Congenital hypoplastic anemia", "congenital hypoplastic anemia", "Hypoplastic anemia - familial", "Congenital Hypoplastic Anemia", "Congenital Hypoplastic Anemias", "congenital hypoplastic anaemia", "Hypoplastic Anemia, Congenital", "Hypoplastic anaemia - familial", "Constitutional aplastic anemia", "constitutional aplastic anemia", "Congenital hypoplastic anaemia", "Anemia, Congenital Hypoplastic", "Constitutional aplastic anaemia", "Anemia, Hypoplastic, Congenital", "Aplastic anemia, constitutional", "Hypoplastic Anemias, Congenital", "constitutional aplastic anaemia", "Anemias, Congenital Hypoplastic", "anemia; aplastic, constitutional", "aplastic; anemia, constitutional", "rare constitutional aplastic anemia", "Constitutional aplastic anemia, NOS", "Constitutional aplastic anaemia, NOS", "familial hypoplastic anemia (diagnosis)", "Constitutional aplastic anemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited aplastic anemia", "shortest_name_length": 25}
{"curie": "MONDO:0003315", "names": ["stage 0 uterine cancer", "uterine cancer, stage 0", "Endometrial cancer stage 0", "stage 0 endometrial cancer", "endometrial cancer, stage 0", "Endometrial carcinoma stage 0", "endometrium in situ carcinoma", "endometrial carcinoma in situ", "Cancer of endometrium stage 0", "stage 0 endometrium carcinoma", "Carcinoma endometrial stage 0", "endometrium carcinoma in situ", "stage 0 endometrial carcinoma", "endometrial carcinoma, stage 0", "Carcinoma in situ of endometrium", "carcinoma in situ of endometrium", "stage 0 cancer of the endometrium", "cancer of the endometrium, stage 0", "stage 0 carcinoma of the endometrium", "carcinoma of the endometrium, stage 0", "Carcinoma in situ of endometrium (disorder)", "carcinoma in situ of endometrium (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometrium carcinoma in situ", "shortest_name_length": 22}
{"curie": "MONDO:0013975", "names": ["ECTD7", "ectodermal dysplasia 7", "ECTODERMAL DYSPLASIA 7, HAIR/NAIL TYPE", "ectodermal dysplasia 7, hair/nail type", "KRT74 pure hair and nail ectodermal dysplasia", "pure hair and nail ectodermal dysplasia caused by mutation in KRT74"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia 7, hair/nail type", "shortest_name_length": 5}
{"curie": "MONDO:0001370", "names": ["Pericardial fluid", "pericardial fluid", "Pericardial Fluid", "Fluid around heart", "FLUID, PERICARDIAL", "fluid, pericardial", "Effusion pericardial", "Fluid in pericardium", "pericardial effusion", "Pericardial Effusion", "effusion pericardial", "Pericardial effusion", "EFFUSION PERICARDIAL", "PERICARDIAL EFFUSION", "PERICARDIAL_EFFUSION", "effusion; pericardial", "pericardium; effusion", "Effusion, Pericardial", "pericardial effusions", "Pericardial Effusions", "Pericardial effusions", "effusion; pericardium", "Effusions, Pericardial", "Pericardial effusion, NOS", "pericardial effusion (disease)", "Pericardial effusion (disorder)", "pericardial effusion (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pericardial effusion", "shortest_name_length": 17}
{"curie": "MONDO:0008536", "names": ["temperature-sensitive lethal mutation", "TEMPERATURE-SENSITIVE LETHAL MUTATION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "temperature-sensitive lethal mutation", "shortest_name_length": 37}
{"curie": "MONDO:0012940", "names": ["IBD24", "INFLAMMATORY BOWEL DISEASE 24", "Inflammatory Bowel Disease 24", "inflammatory bowel disease 24", "inflammatory bowel disease type 24"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory bowel disease 24", "shortest_name_length": 5}
{"curie": "MONDO:0018105", "names": ["WFS", "DIDMOAD", "didmoad", "DIDMOADUD", "DIDMOAD Syndrome", "didmoad syndrome", "wolfram syndrome", "Wolfram syndrome", "DIDMOAD syndrome", "Wolfram Syndrome", "Syndrome, Wolfram", "Marquardt-Loriaux syndrome", "diabetes insipidus-diabetes mellitus-optic atrophy syndrome", "Diabetes Insipidus and Mellitus with Optic Atrophy and Deafness", "Diabetes mellitus AND insipidus with optic atrophy AND deafness", "diabetes insipidus and mellitus with optic atrophy and deafness", "DIABETES INSIPIDUS AND MELLITUS WITH OPTIC ATROPHY AND DEAFNESS", "Diabetes mellitus and insipidus with optic atrophy and deafness", "diabetes mellitus and insipidus with optic atrophy and deafness", "Diabetes insipidus,diabetes mellitus, optic atrophy and deafness", "Diabetes insipidus, diabetes mellitus, optic atrophy and deafness", "Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, and Deafness", "diabetes insipidus-diabetes mellitus-optic atrophy (DIDMO) syndrome", "diabetes insipidus-diabetes mellitus-optic atrophy-deafness syndrome", "Diabetes insipidus-diabetes mellitus-optic atrophy-deafness syndrome", "Diabetes insipidus-diabetes mellitus-optic atrophy-hearing loss syndrome", "diabetes insipidus and mellitus with optic atrophy and deafness (DIDMOAD)", "Diabetes mellitus AND insipidus with optic atrophy AND deafness (disorder)", "DIDMOAD - Diabetes insipidus,diabetes mellitus, optic atrophy and deafness", "Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, and Deafness Syndrome", "DIDMOAD - Diabetes insipidus, diabetes mellitus, optic atrophy and deafness", "diabetes mellitus and insipidus with optic atrophy and deafness (diagnosis)", "diabetes insipidus, diabetes mellitus, optic atrophy, and deafness syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wolfram syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0015330", "names": ["overgrowth/obesity syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "overgrowth/obesity syndrome", "shortest_name_length": 27}
{"curie": "UMLS:C5237306", "names": ["Refractory Thyroid Gland Papillary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Thyroid Gland Papillary Carcinoma", "shortest_name_length": 44}
{"curie": "UMLS:C0751830", "names": ["Neurologic Gait Disorder", "Neurologic Gait Disorders", "Gait Disorder, Neurologic", "Gait Disorders, Neurologic", "Neurologic Gait Dysfunction", "Gait Dysfunction, Neurologic", "Neurologic Gait Dysfunctions", "Gait Dysfunctions, Neurologic", "Neurologic Ambulation Disorder", "Neurologic Locomotion Disorder", "Ambulation Disorder, Neurologic", "Neurologic Ambulation Disorders", "Locomotion Disorder, Neurologic", "Neurologic Locomotion Disorders", "Locomotion Disorders, Neurologic", "Ambulation Disorders, Neurologic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gait Disorders, Neurologic", "shortest_name_length": 24}
{"curie": "UMLS:C0034350", "names": ["Pyruvate Metabolism, Inborn Errors", "Inborn error of pyruvate metabolism", "Inborn error of pyruvate metabolism, NOS", "Inborn error of pyruvate metabolism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pyruvate Metabolism, Inborn Errors", "shortest_name_length": 34}
{"curie": "UMLS:C1515862", "names": ["Acinar Prostate Adenocarcinoma, Atrophic Variant", "Prostate Acinar Adenocarcinoma, Atrophic Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Acinar Adenocarcinoma, Atrophic Variant", "shortest_name_length": 48}
{"curie": "MONDO:0010199", "names": ["white forelock with malformations", "White forelock with malformations", "WHITE FORELOCK WITH MALFORMATIONS", "White forelock with malformations syndrome", "White forelock with malformations syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "white forelock with malformations", "shortest_name_length": 33}
{"curie": "UMLS:C2347924", "names": ["Refractory Central Nervous System Neoplasm", "Refractory Primary Central Nervous System Tumor", "Refractory Primary Central Nervous System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Primary Central Nervous System Neoplasm", "shortest_name_length": 42}
{"curie": "MONDO:0021670", "names": ["post-infectious syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "post-infectious syndrome", "shortest_name_length": 24}
{"curie": "MONDO:0020161", "names": ["congenital ectropion", "Congenital ectropion", "ectropion; congenital", "congenital; ectropion", "Congenital ectropion (disorder)", "congenital ectropion (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital ectropion", "shortest_name_length": 20}
{"curie": "UMLS:C1970270", "names": ["Choreoathetosis And Congenital Hypothyroidism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Choreoathetosis And Congenital Hypothyroidism", "shortest_name_length": 45}
{"curie": "MONDO:0100247", "names": ["multiple congenital anomalies-hypotonia-seizures syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple congenital anomalies-hypotonia-seizures syndrome", "shortest_name_length": 57}
{"curie": "MONDO:0007209", "names": ["WNS", "Toxopachyosteosis", "Weismann-Netter Syndrome", "WEISMANN-NETTER syndrome", "Weismann-Netter syndrome", "Weismann Netter syndrome", "WEISMANN-NETTER SYNDROME", "Weismann Netter Stuhl syndrome", "Weismann-Netter-Stuhl syndrome", "Weismann Netter syndrome (disorder)", "Anterior bowing of legs with dwarfism", "anterior bowing of legs with dwarfism", "bowing of legs, anterior with dwarfism", "BOWING OF LEGS, ANTERIOR, WITH DWARFISM", "bowing of legs, anterior, with dwarfism", "Bowing of legs, anterior, with dwarfism", "Toxopachyoteose diaphysaire tibio peroniere", "Toxopachyosteose Diaphysaire Tibio-Peroniere", "Toxopachyosteose diaphysaire tibio-peroniere", "TOXOPACHYOSTEOSE DIAPHYSAIRE TIBIO-PERONIERE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Weismann-Netter syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C5205066", "names": ["Refractory Non-GC/ABC DLBCL", "Refractory Diffuse Large B-Cell Lymphoma Non-GC/ABC", "Refractory Diffuse Large B-Cell Lymphoma Activated B-Cell Type", "Refractory Diffuse Large B-Cell Lymphoma Non-Germinal Center/Activated B-Cell Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Diffuse Large B-Cell Lymphoma Activated B-Cell Type", "shortest_name_length": 27}
{"curie": "MONDO:0006229", "names": ["STSC", "gastric Oat cell carcinoma", "Gastric Oat Cell Carcinoma", "stomach small cell carcinoma", "Gastric Small Cell Carcinoma", "gastric small cell carcinoma", "Oat Cell Carcinoma of Stomach", "Oat cell carcinoma of stomach", "small cell carcinoma of stomach", "Small Cell Carcinoma of Stomach", "Oat Cell Carcinoma of the Stomach", "Oat cell carcinoma of the stomach", "Small Cell Carcinoma of the Stomach", "small cell carcinoma of the stomach", "gastric small cell neuroendocrine carcinoma", "small cell carcinoma of stomach (diagnosis)", "Gastric Small Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric small cell neuroendocrine carcinoma", "shortest_name_length": 4}
{"curie": "UMLS:C0153071", "names": ["Mosquito-Borne Hemorrhagic Fever", "mosquito-borne hemorrhagic fever", "Mosquito-borne hemorrhagic fever", "Mosquito-borne haemorrhagic fever", "mosquito-borne; hemorrhagic fever", "hemorrhagic fever; mosquito-borne", "fever; mosquito-borne, hemorrhagic", "mosquito-borne hemorrhagic fever (diagnosis)", "Mosquito-borne hemorrhagic fever (navigational concept)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mosquito-borne hemorrhagic fever", "shortest_name_length": 32}
{"curie": "MONDO:0017322", "names": ["disorders of vitamin D metabolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorders of vitamin D metabolism", "shortest_name_length": 33}
{"curie": "MONDO:0015799", "names": ["Smith-McCort dwarfism", "Smith McCort dysplasia", "Smith-McCort dysplasia", "Smith-McCort Dysplasia", "SMITH-MCCORT DYSPLASIA", "Smith McCort dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Smith-McCort dysplasia", "shortest_name_length": 21}
{"curie": "MONDO:0011168", "names": ["T1D10", "IDDM10", "type 1 diabetes mellitus 10", "TYPE 1 DIABETES MELLITUS 10", "IL2RA type 1 diabetes mellitus", "Insulin-Dependent Diabetes Mellitus 10", "INSULIN-DEPENDENT DIABETES MELLITUS 10", "insulin-dependent diabetes mellitus 10", "DIABETES MELLITUS, INSULIN-DEPENDENT, 10", "Diabetes Mellitus, Insulin-Dependent, 10", "diabetes mellitus, insulin-dependent, 10", "diabetes mellitus, insulin-dependent, type 10", "type 1 diabetes mellitus caused by mutation in IL2RA", "diabetes, mellitus, insulin-dependent, susceptibility to, 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type 1 diabetes mellitus 10", "shortest_name_length": 5}
{"curie": "UMLS:C0279623", "names": ["M1", "adult acute M1 leukemia", "M1 leukemia, adult acute", "M1 Adult Acute Myeloid Leukemia", "Adult Acute Myeloblastic Leukemia", "M1 Adult Acute Myelocytic Leukemia", "M1 Adult Acute Myelogenous Leukemia", "M1 Adult Acute Myeloblastic Leukemia", "M1 Adult Acute Granulocytic Leukemia", "Adult Acute Myeloid Leukemia without Maturation", "Acute Myeloid Leukemia (AML) without Maturation", "M1 Adult Acute Myeloid Leukemia without Maturation", "Adult Acute Myelogenous Leukemia without Maturation", "Adult Acute Granulocytic Leukemia without Maturation", "Adult Acute Myeloblastic Leukemia without Maturation", "M1 Adult Acute Myelogenous Leukemia without Maturation", "M1 adult acute myeloblastic leukemia without maturation", "M1 Adult Acute Granulocytic Leukemia without Maturation", "Adult Acute Myeloblastic Leukemia without Maturation (M1)", "adult acute myeloblastic leukemia without maturation (M1)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Acute Myeloid Leukemia without Maturation", "shortest_name_length": 2}
{"curie": "MONDO:0017920", "names": ["Pfeiffer-Kapferer syndrome", "Pfeiffer Kapferer syndrome", "Short stature, mental retardation and multiple dysmorphisms", "short stature, mental retardation and multiple dysmorphisms", "short stature, intellectual disability and multiple dysmorphisms", "Deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome", "deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome", "Deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome", "deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome", "Hearing loss-genital anomalies-metacarpal and metatarsal synostosis syndrome", "Deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome (disorder)", "deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome (diagnosis)", "sensorineural deafness, hypospadias, and synostosis of metacarpals and metatarsals 4 and 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome", "shortest_name_length": 26}
{"curie": "UMLS:C0392452", "names": ["CRANIOTABES", "Craniotabes", "craniotabes", "Neonatal craniotabes", "craniotabes was seen", "neonatal; craniotabes", "craniotabes; neonatal", "Craniotabes (disorder)", "craniotabes (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Craniotabes", "shortest_name_length": 11}
{"curie": "MONDO:0001339", "names": ["pylethrombosis", "Pylethrombosis", "Thrombosis;portal", "portal thrombosis", "portal; thrombosis", "thrombosis; portal", "portal thrombosis vein", "thrombosis portal vein", "Portal vein thrombosis", "Thrombosis portal vein", "portal vein thrombosis", "Portal Vein Thrombosis", "THROMBOSIS, PORTAL VEIN", "Blood clot in portal vein", "thrombosis of portal vein", "PVT - Portal vein thrombosis", "Thrombosis of the portal vein", "portal vein thrombotic disease", "Primitive portal vein thrombosis", "Portal vein thrombosis (disorder)", "thrombotic disease of portal vein", "Deep vein thrombosis of portal vein", "Non-cirrhotic portal vein thrombosis", "thrombosis of portal vein (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "portal vein thrombosis", "shortest_name_length": 14}
{"curie": "MONDO:0016447", "names": ["white fibrous papulosis of the neck"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "white fibrous papulosis of the neck", "shortest_name_length": 35}
{"curie": "MONDO:0007858", "names": ["KPPP1", "Kppp1", "PPKP1", "PPKP1A", "Buschke-Fischer-Brauer syndrome", "Buschke Fischer Brauer syndrome", "Keratosis palmoplantaris papulosa", "KERATOSIS PALMOPLANTARIS PAPULOSA", "keratosis palmoplantaris papulosa", "AAGAB punctate palmoplantar keratoderma", "Type I punctate palmoplantar keratoderma", "punctate palmoplantar keratoderma type I", "Punctate palmoplantar keratoderma type 1", "punctate palmoplantar keratoderma type 1A", "punctate palmoplantar keratoderma type 1B", "palmoplantar keratoderma, punctate type 1", "Keratoderma, palmoplantar punctate type 1", "PALMOPLANTAR KERATODERMA, PUNCTATE TYPE I", "Keratoderma, Palmoplantar, Punctate Type I", "palmoplantar keratoderma, punctate type IA", "palmoplantar keratoderma, punctate type 1A", "PALMOPLANTAR KERATODERMA, PUNCTATE TYPE IA", "keratoderma, palmoplantar, punctate type IA", "KERATODERMA, PALMOPLANTAR, PUNCTATE TYPE IA", "hereditary palmoplantar keratoderma punctate type 1", "Punctate palmoplantar keratoderma type 1 (disorder)", "Punctate palmoplantar keratoderma type 1 (diagnosis)", "punctate palmoplantar keratoderma caused by mutation in AAGAB", "Keratodermia palmoplantaris papulosa Buschke Fischer Brauer type", "KERATODERMIA PALMOPLANTARIS PAPULOSA, BUSCHKE-FISCHER-BRAUER TYPE", "Keratodermia palmoplantaris papulosa, Buschke-Fischer-Brauer type", "keratodermia palmoplantaris papulosa, Buschke-Fischer-Brauer type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "palmoplantar keratoderma, punctate type 1A", "shortest_name_length": 5}
{"curie": "MONDO:0018665", "names": ["X-linked acrogigantism due to a point mutation", "familial infantile gigantism due to a point mutation", "X-LAG (X-linked acrogigantism) due to a point mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked acrogigantism due to a point mutation", "shortest_name_length": 46}
{"curie": "MONDO:0012955", "names": ["LNCR4", "lung cancer susceptibility 4", "LUNG CANCER SUSCEPTIBILITY 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung cancer susceptibility 4", "shortest_name_length": 5}
{"curie": "UMLS:C0857807", "names": ["accidental ingestion", "Accidental ingestion", "accidental ingestions", "accidental ingestion (history)", "Accidental ingestion of potentially harmful entity", "Accidental ingestion of potentially harmful entity (event)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Accidental ingestion", "shortest_name_length": 20}
{"curie": "MONDO:0008113", "names": ["SBRS", "BRSS", "SCHILBACH-ROTT SYNDROME", "Schilbach-Rott syndrome", "Schilbach Rott syndrome", "Schilbach-Rott Syndrome", "blepharofacioskeletal syndrome", "Blepharofacioskeletal Syndrome", "BLEPHAROFACIOSKELETAL SYNDROME", "Schilbach Rott syndrome (disorder)", "hypotelorism cleft palate hypospadias", "Cleft Palate, Hypotelorism, and Hypospadias", "cleft palate, hypotelorism, and hypospadias", "CLEFT PALATE, HYPOTELORISM, AND HYPOSPADIAS", "hypotelorism-cleft palate-hypospadias syndrome", "Hypotelorism-cleft palate-hypospadias syndrome", "Hypotelorism, cleft palate, hypospadias syndrome", "ocular hypotelorism, submucosal cleft palate, and hypospadias", "Ocular Hypotelorism, Submucosal Cleft Palate, and Hypospadias", "OCULAR HYPOTELORISM, SUBMUCOSAL CLEFT PALATE, AND HYPOSPADIAS", "Schilbach-Rott Syndrome Ocular Hypotelorism, Submucosal Cleft Palate, and Hypospadias"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Schilbach-Rott syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C1336746", "names": ["Thymus Carcinoid", "Thymic Carcinoid", "Thymus Carcinoid Tumor", "Thymic Carcinoid Tumor", "Carcinoid Tumor of Thymus", "Carcinoid Tumor of the Thymus", "Malignant carcinoid tumor of thymus", "malignant carcinoid tumor of thymus", "Malignant carcinoid tumour of thymus", "Malignant carcinoid tumor of the thymus", "Malignant carcinoid tumor of thymus (disorder)", "malignant carcinoid tumor of thymus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thymic Carcinoid Tumor", "shortest_name_length": 16}
{"curie": "MONDO:0019234", "names": ["ZSD", "PBD", "PBD-ZSS", "PBD-ZSD", "PBD, ZSS", "Zellweger Spectrum", "Zellweger spectrum", "Spectrum, Zellweger", "Zellweger leukodystrophy", "Zellweger Syndrome Spectrum", "Zellweger spectrum disorder", "cerebrohepatorenal syndrome", "Zellweger Spectrum Disorder", "Zellweger syndrome spectrum", "Zellweger spectrum disorders", "Peroxisome biogenesis disorder", "Peroxisome Biogenesis Disorder", "peroxisome biogenesis disorder", "peroxisomal biogenesis disorder", "Peroxisome biogenesis disorders", "PBD-Zellweger spectrum disorder", "peroxisomal biogenesis disorders", "disorders of peroxisome biogenesis", "Disorders of peroxisome biogenesis", "Zellweger syndrome spectrum (diagnosis)", "Peroxisome biogenesis disorder spectrum", "peroxisome biogenesis disorder spectrum", "Peroxisome biogenesis disorder (disorder)", "Peroxisome Biogenesis Disorders in the Zellweger Spectrum", "Peroxisome biogenesis disorder-Zellweger spectrum disorder", "peroxisome biogenesis disorder-Zellweger syndrome spectrum", "Peroxisome Biogenesis Disorders, Zellweger Syndrome Spectrum", "peroxisome biogenesis disorders, Zellweger syndrome spectrum", "peroxisomal biogenesis disorders, Zellweger syndrome spectrum", "PBD-ZSS - Peroxisome biogenesis disorder Zellweger syndrome spectrum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder", "shortest_name_length": 3}
{"curie": "MONDO:0030748", "names": ["JEB3A", "epidermolysis bullosa, junctional 3A, intermediate", "EPIDERMOLYSIS BULLOSA, JUNCTIONAL 3A, INTERMEDIATE", "epidermolysis bullosa, junctional 3A, non-herlitz IIA", "EPIDERMOLYSIS BULLOSA, JUNCTIONAL 3A, NON-HERLITZ TYPE", "epidermolysis bullosa, junctional 3A, generalized intermediate", "EPIDERMOLYSIS BULLOSA, JUNCTIONAL 3A, GENERALIZED INTERMEDIATE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolysis bullosa, junctional 3A, intermediate", "shortest_name_length": 5}
{"curie": "MONDO:0011629", "names": ["CDG2B", "CDG 2B", "CDGIIB", "CDGIIb", "CDG-IIb", "CDG IIB", "CDG IIb", "MOGS-CDG", "GCS1-CDG", "MOGS-CDG (CDG-IIb)", "CDG syndrome type IIb", "glucosidase 1 deficiency", "glucosidase I deficiency", "GLUCOSIDASE I DEFICIENCY", "Glucosidase I Deficiency", "Glucosidase 1 deficiency", "MOGS-congenital disorder of glycosylation", "congenital disorder of glycosylation type 2b", "Congenital disorder of glycosylation type 2b", "congenital disorder of glycosylation type IIb", "Congenital disorder of glycosylation type IIb", "Congenital Disorder Of Glycosylation, Type IIB", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIb", "congenital disorder of glycosylation, type IIb", "Carbohydrate deficient glycoprotein syndrome type IIb", "carbohydrate deficient glycoprotein syndrome type IIb", "Mannosyl-oligosaccharide glycosidase congenital disorder of glycosylation", "mannosyl-oligosaccharide glycosidase congenital disorder of glycosylation", "Mannosyl-oligosaccharide glycosidase congenital disorder of glycosylation (disorder)", "MOGS CDG - mannosyl-oligosaccharide glycosidase congenital disorder of glycosylation", "mannosyl-oligosaccharide glycosidase congenital disorder of glycosylation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MOGS-congenital disorder of glycosylation", "shortest_name_length": 5}
{"curie": "UMLS:C0333411", "names": ["Pseudocholesteatoma", "cholesterol granuloma", "Cholesterol granuloma", "Cholesterol Granuloma", "Cholesterinic granuloma", "Cholesterol granuloma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cholesterol granuloma", "shortest_name_length": 19}
{"curie": "MONDO:0035220", "names": ["PLG-related HAE with normal C1 inhibitor", "PLG-related hereditary angioedema with normal C1inh"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PLG-related hereditary angioedema with normal C1inh", "shortest_name_length": 40}
{"curie": "MONDO:0021908", "names": ["aplasia cutis congenita dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aplasia cutis congenita dominant", "shortest_name_length": 32}
{"curie": "MONDO:0011251", "names": ["facial dysmorphism, cleft palate, hearing loss, and camptodactyly", "Facial Dysmorphism, Cleft Palate, Hearing Loss, and Camptodactyly", "FACIAL DYSMORPHISM, CLEFT PALATE, HEARING LOSS, AND CAMPTODACTYLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "facial dysmorphism, cleft palate, hearing loss, and camptodactyly", "shortest_name_length": 65}
{"curie": "MONDO:0004396", "names": ["Cervical Intraspinal Meningioma", "cervical intraspinal meningioma", "Cervical Spinal Canal and Spinal Cord Meningioma", "cervical spinal canal and spinal cord meningioma", "meningioma of cervical spinal canal and spinal cord", "Meningioma of Cervical Spinal Canal and Spinal Cord", "meningioma of the cervical Spinal canal and Spinal Cord", "Meningioma of the Cervical Spinal Canal and Spinal Cord", "meningioma of the cervical spinal canal and spinal cord"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical spinal canal and spinal cord meningioma", "shortest_name_length": 31}
{"curie": "MONDO:0008651", "names": ["VERTEBRAL HYPOPLASIA WITH LUMBAR KYPHOSIS", "vertebral hypoplasia with lumbar kyphosis", "Vertebral Hypoplasia With Lumbar Kyphosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vertebral hypoplasia with lumbar kyphosis", "shortest_name_length": 41}
{"curie": "MONDO:0003109", "names": ["Foramen Magnum Meningioma", "foramen magnum meningioma", "meningioma of Foramen magnum", "Meningioma of Foramen Magnum", "meningioma of foramen magnum", "Meningioma of the Foramen Magnum", "meningioma of the Foramen magnum", "meningioma of the Foramen Magnum", "foramen magnum meningioma (disease)", "meningioma (disease) of foramen magnum", "meningioma of foramen magnum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "foramen magnum meningioma", "shortest_name_length": 25}
{"curie": "MONDO:0014309", "names": ["MOSPGF", "obesity due to CEP19 deficiency", "MORBID OBESITY AND SPERMATOGENIC FAILURE", "morbid obesity and spermatogenic failure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "obesity due to CEP19 deficiency", "shortest_name_length": 6}
{"curie": "MONDO:0011611", "names": ["short stature, mental retardation, callosal agenesis, Heminasal hypoplasia, microphthalmia, and atypical clefting", "Short Stature, Mental Retardation, Callosal Agenesis, Heminasal Hypoplasia, Microphthalmia, And Atypical Clefting", "SHORT STATURE, MENTAL RETARDATION, CALLOSAL AGENESIS, HEMINASAL HYPOPLASIA, MICROPHTHALMIA, AND ATYPICAL CLEFTING", "short stature, intellectual disability, callosal agenesis, Heminasal hypoplasia, microphthalmia, and atypical clefting", "SHORT STATURE, IMPAIRED INTELLECTUAL DEVELOPMENT, CALLOSAL AGENESIS, HEMINASAL HYPOPLASIA, MICROPHTHALMIA, AND ATYPICAL CLEFTING"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short stature, intellectual disability, callosal agenesis, Heminasal hypoplasia, microphthalmia, and atypical clefting", "shortest_name_length": 113}
{"curie": "UMLS:C0264344", "names": ["septic bronchitis", "Septic bronchitis", "septic; bronchitis", "bronchitis; septic", "Bronchitis bacterial", "BRONCHITIS BACTERIAL", "bacterial bronchitis", "Bronchitis bacterial NOS", "Septic bronchitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Septic bronchitis", "shortest_name_length": 17}
{"curie": "UMLS:C0278649", "names": ["Recurrent Rhabdomyosarcoma", "Relapsed Pediatric Rhabdomyosarcoma", "Relapsed Childhood Rhabdomyosarcoma", "Recurrent Pediatric Rhabdomyosarcoma", "recurrent childhood rhabdomyosarcoma", "Recurrent Childhood Rhabdomyosarcoma", "recurrent pediatric rhabdomyosarcoma", "rhabdomyosarcoma, recurrent childhood", "childhood rhabdomyosarcoma, recurrent", "pediatric rhabdomyosarcoma, recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Rhabdomyosarcoma", "shortest_name_length": 26}
{"curie": "UMLS:C0016124", "names": ["FINGER INJURY", "Finger injury", "finger injury", "injury finger", "Finger Injury", "Injury, Finger", "injury; finger", "finger injuries", "Finger Injuries", "Injuries, Finger", "Injury;finger(s)", "Injury of finger", "finger(s); injury", "injury of fingers", "Injury to finger NOS", "Injury of finger (disorder)", "injury of fingers (diagnosis)", "Finger Injuries and Disorders", "Other and unspecified injury to finger"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Finger Injuries", "shortest_name_length": 13}
{"curie": "MONDO:0100291", "names": ["ETP-ALL", "ETP ALL", "early T acute lymphoblastic leukemia", "Early T-Acute Lymphoblastic Leukemia", "Early T Acute Lymphoblastic Leukemia", "early T-cell precursor lymphoblastic leukemia", "Early T-Cell Precursor Lymphoblastic Leukemia", "Early T-Cell Precursor Acute Lymphoblastic Leukemia", "early T-cell precursor acute lymphoblastic leukemia", "early T cell progenitor acute lymphoblastic leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early T cell progenitor acute lymphoblastic leukemia", "shortest_name_length": 7}
{"curie": "UMLS:C2931784", "names": ["Amyloid angiopathy", "Amyloidosis - cerebral", "Senile cerebral amyloid angiopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Amyloid angiopathy", "shortest_name_length": 18}
{"curie": "UMLS:C5420759", "names": ["Conjunctival Sebaceous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conjunctival Sebaceous Carcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C1096387", "names": ["Chemical eye injury", "chemical eye injury", "chemical eye injuries", "chemicals eye injuries"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chemical eye injury", "shortest_name_length": 19}
{"curie": "MONDO:0700199", "names": ["Sheep Lung Adenocarcinoma", "sheep lung adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sheep lung adenocarcinoma", "shortest_name_length": 25}
{"curie": "UMLS:C0406766", "names": ["Palmoplantar keratoderma with leucoplakia", "Palmoplantar Keratoderma with Leukoplakia", "Palmoplantar keratoderma with leukoplakia", "Palmoplantar keratoderma with leukoplakia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Palmoplantar keratoderma with leukoplakia", "shortest_name_length": 41}
{"curie": "MONDO:0015175", "names": ["AIP", "autoimmune pancreatitis", "Autoimmune Pancreatitis", "Autoimmune pancreatitis", "Pancreatitis, Autoimmune", "Autoimmune Pancreatitides", "Autoimmune pancreatitis (disorder)", "lymphoplasmocytic sclerosing pancreatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune pancreatitis", "shortest_name_length": 3}
{"curie": "MONDO:0012832", "names": ["IBD14", "Ibd14", "INFLAMMATORY BOWEL DISEASE 14", "inflammatory bowel disease 14", "Inflammatory Bowel Disease 14", "IRF5 inflammatory bowel disease", "inflammatory bowel disease type 14", "inflammatory bowel disease caused by mutation in IRF5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory bowel disease 14", "shortest_name_length": 5}
{"curie": "MONDO:0019211", "names": ["isolated anonychia", "congenital anonychia", "isolated congenital anonychia", "nonsyndromic congenital nail disorder, 4", "autosomal recessive nonsyndromic congenital nail disorder-4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated congenital anonychia", "shortest_name_length": 18}
{"curie": "MONDO:0006758", "names": ["female genital tuberculosis", "Female Genital Tuberculoses", "Female Genital Tuberculosis", "tuberculosis female genital", "Genital Tuberculosis, Female", "Tuberculoses, Female Genital", "Tuberculosis, Female Genital", "Genital Tuberculoses, Female", "Female genital tract tuberculosis", "tuberculosis female genital organs", "Female genital tract tuberculosis NOS", "Tuberculosis of female genital organs", "tuberculosis female genital organs (diagnosis)", "Tuberculosis of female genital organs (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "female genital tuberculosis", "shortest_name_length": 27}
{"curie": "UMLS:C5420224", "names": ["Oral Cavity Myofibroblastic Sarcoma", "Oral Cavity Low Grade Myofibroblastic Sarcoma", "Oral Cavity Low-Grade Myofibroblastic Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral Cavity Low Grade Myofibroblastic Sarcoma", "shortest_name_length": 35}
{"curie": "MONDO:0013715", "names": ["ALS16", "ALS16 (diagnosis)", "amyotrophic lateral sclerosis 16", "amyotrophic lateral sclerosis ALS16", "SIGMAR1 amyotrophic lateral sclerosis", "amyotrophic lateral sclerosis type 16", "AMYOTROPHIC LATERAL SCLEROSIS 16, JUVENILE", "amyotrophic lateral sclerosis 16, juvenile", "amyotrophic lateral sclerosis caused by mutation in SIGMAR1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyotrophic lateral sclerosis type 16", "shortest_name_length": 5}
{"curie": "MONDO:0054781", "names": ["COXPD36", "combined oxidative phosphorylation deficiency 36", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 36"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation deficiency 36", "shortest_name_length": 7}
{"curie": "MONDO:0006382", "names": ["PDTC", "Insular carcinoma", "insular carcinoma", "Insular Carcinoma", "insular thyroid cancer", "poorly differentiated thyroid cancer", "poorly differentiated thyroid carcinoma", "Poorly differentiated thyroid carcinoma", "Poorly Differentiated Thyroid Carcinoma", "poorly differentiated thyroid gland cancer", "Poorly Differentiated Thyroid Gland Cancer", "Insular carcinoma (morphologic abnormality)", "thyroid gland poorly differentiated carcinoma", "Poorly Differentiated Thyroid Gland Carcinoma", "poorly differentiated thyroid gland carcinoma", "Thyroid Gland Poorly Differentiated Carcinoma", "poorly differentiated carcinoma of thyroid gland", "Poorly Differentiated Carcinoma of Thyroid Gland", "poorly differentiated carcinoma of the thyroid gland", "Poorly Differentiated Carcinoma of the Thyroid Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "poorly differentiated thyroid gland carcinoma", "shortest_name_length": 4}
{"curie": "UMLS:C5206646", "names": ["Primary Peritoneal Undifferentiated Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Peritoneal Undifferentiated Carcinoma", "shortest_name_length": 45}
{"curie": "UMLS:C5206759", "names": ["Metastatic Thyroid Gland Medullary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Thyroid Gland Medullary Carcinoma", "shortest_name_length": 44}
{"curie": "UMLS:C4525092", "names": ["Stage IIIB Colorectal Cancer AJCC v8", "Stage IIIB Colorectal Carcinoma AJCC v8", "Stage IIIB Colorectal (Colon or Rectal) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Colorectal Cancer AJCC v8", "shortest_name_length": 36}
{"curie": "MONDO:0008103", "names": ["NODULI CUTANEI, MULTIPLE, WITH URINARY TRACT ABNORMALITIES", "Noduli Cutanei, Multiple, with Urinary Tract Abnormalities", "noduli Cutanei, multiple, with urinary tract abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "noduli Cutanei, multiple, with urinary tract abnormalities", "shortest_name_length": 58}
{"curie": "UMLS:C3501249", "names": ["Nephrotic Syndrome, Congenital, With Ocular Abnormalities And Congenital Myasthenic Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome, Congenital, With Ocular Abnormalities And Congenital Myasthenic Syndrome", "shortest_name_length": 92}
{"curie": "MONDO:0008668", "names": ["VWD1", "VWD type 1", "VWD, type 1", "VWD, TYPE 1", "von Willebrand disease 1", "von Willebrand's disease 1", "von willebrand's disease 1", "von Willebrand disease type I", "von Willebrand disease type 1", "Type I von Willebrand Disease", "Von Willebrand disease type 1", "Type 1 von Willebrand Disease", "Von Willebrand disease, type 1", "von Willebrand Disease, Type 1", "von Willebrand Disease, Type I", "VON WILLEBRAND DISEASE, TYPE 1", "VON WILLEBRAND disease, type 1", "VON WILLEBRAND DISEASE, TYPE I", "von Willebrand's disease type 1", "Hereditary von Willebrand disease type 1", "von Willebrand disease type 1 (diagnosis)", "Hereditary von Willebrand disease type 1 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "von Willebrand disease 1", "shortest_name_length": 4}
{"curie": "UMLS:C4683565", "names": ["Lugano Classification Adult Lymphoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Adult Lymphoma by AJCC v8 Stage", "shortest_name_length": 53}
{"curie": "UMLS:C0263445", "names": ["Acne fulminans", "acne fulminans", "Acne fulminans (disorder)", "acne fulminans (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acne fulminans", "shortest_name_length": 14}
{"curie": "MONDO:0015806", "names": ["infant-like botulism", "Infant-like botulism", "adult intestinal botulism", "Adult Intestinal Botulism", "Adult intestinal botulism", "intestinal botulism of adults", "Adult Intestinal Toxemia Botulism", "adult intestinal toxemia botulism", "Adult intestinal toxemia botulism", "Adult intestinal colonization botulism", "adult intestinal colonization botulism", "adult intestinal toxin-mediated botulism", "Adult intestinal toxin-mediated botulism", "Adult infection of intestine caused by Clostridium botulinum", "Adult infection of intestine caused by Clostridium botulinum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult intestinal botulism", "shortest_name_length": 20}
{"curie": "UMLS:C2984118", "names": ["Laryngeal Cancer by AJCC v7 Stage", "Laryngeal Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laryngeal Cancer by AJCC v7 Stage", "shortest_name_length": 33}
{"curie": "UMLS:C0333386", "names": ["Lymphorrhage", "lymphocytic infiltrate", "Lymphocytic Infiltrate", "Lymphocytic infiltrate", "infiltrate lymphocytic", "lymphocytic infiltrates", "Lymphocytic infiltration", "Lymphocytic infiltrates NOS", "Lymphocytic infiltrate, NOS", "Chronic lymphocytic inflammation", "Chronic lymphocytic inflammation, NOS", "Lymphocytic inflammatory cell infiltrate", "Lymphocytic inflammatory cell infiltrate, NOS", "Chronic lymphocytic inflammation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic lymphocytic inflammation", "shortest_name_length": 12}
{"curie": "MONDO:0012222", "names": ["KANZAKI disease", "KANZAKI DISEASE", "Kanzaki disease", "NAGA deficiency type 2", "Naga deficiency, type 2", "Schindler disease type 2", "NAGA Deficiency, Type II", "NAGA DEFICIENCY, TYPE II", "Schindler disease, type 2", "SCHINDLER DISEASE, TYPE II", "Schindler Disease, Type II", "alpha-N-acetylgalactosaminidase deficiency type 2", "Alpha-N-acetylgalactosaminidase deficiency type 2", "Alpha-N-acetylgalactosaminidase deficiency, type 2", "ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, TYPE II", "alpha-N-Acetylgalactosaminidase Deficiency, Type II", "Adult-onset Alpha-N-acetylgalactosaminidase deficiency", "adult-onset Alpha-N-acetylgalactosaminidase deficiency", "adult-onset alpha-N-acetylgalactosaminidase deficiency", "Alpha-N-acetylgalactosaminidase deficiency adult onset", "ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, ADULT-ONSET", "Alpha-N-Acetylgalactosaminidase Deficiency, Adult-Onset", "Alpha-N-acetylgalactosaminidase deficiency, adult-onset", "NAGA (alpha-N-acetylgalactosaminidase) deficiency type 2", "Alpha-N-acetylgalactosaminidase deficiency type 2 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alpha-N-acetylgalactosaminidase deficiency type 2", "shortest_name_length": 15}
{"curie": "UMLS:C1444173", "names": ["Arthropod bite wound", "Arthropod bite wound (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arthropod bite wound", "shortest_name_length": 20}
{"curie": "MONDO:0008437", "names": ["SPG3", "FSP1", "Spg3", "SPG3A", "Spg3a", "Strümpell disease", "Strumpell Disease", "strumpell disease", "Strumpell disease", "STRUMPELL DISEASE", "strumpell's disease", "Strumpell's disease", "Spastic Paraplegia 3", "spastic paraplegia 3", "Spastic Paraplegia 3A", "Spastic Paraplegia 3a", "spastic Paraplegia 3A", "Strumpell-Lorrain disease", "Spastic Paraplegia Type 3a", "SPG3A Spastic paraplegia 3a", "familial spastic paraplegia", "spastic; paralysis, familial", "familial; paralysis, spastic", "paralysis; spastic, familial", "hereditary spastic paraplegia 3A", "Fsp1 Familial spastic paraplegia 1", "ATL1 hereditary spastic paraplegia", "Familial spastic paraplegia syndrome", "hereditary spastic paraplegia type 3A", "autosomal dominant spastic paraplegia 3", "familial spastic paraplegia (diagnosis)", "spastic paraplegia 3, autosomal dominant", "SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT", "Spastic paraplegia 3, autosomal dominant", "spastic paraplegia 3a, autosomal dominant", "autosomal dominant spastic paraplegia type 3", "Autosomal dominant spastic paraplegia type 3", "autosomal dominant familial spastic paraplegia 1", "familial spastic paraplegia, autosomal dominant, 1", "Familial spastic paraplegia, autosomal dominant, 1", "FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 1", "Autosomal dominant spastic paraplegia type 3 (disorder)", "hereditary spastic paraplegia caused by mutation in ATL1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 3A", "shortest_name_length": 4}
{"curie": "UMLS:C1333431", "names": ["EBV Related Lymphoma", "EBV-Related Lymphoma", "EBV-Associated Lymphoma", "Lymphoma, EBV-associated", "Epstein-Barr Virus-Related Lymphoma", "Epstein-Barr Virus Related Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoma, EBV-associated", "shortest_name_length": 20}
{"curie": "UMLS:C5446468", "names": ["Recurrent Anal Canal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Anal Canal Squamous Cell Carcinoma", "shortest_name_length": 44}
{"curie": "MONDO:0008614", "names": ["ST3", "TSHL", "CCTS", "cervical carcinoma", "SUPPRESSOR OF TUMORIGENICITY 3", "suppressor of tumorigenicity 3", "tumor-suppressor Gene, Hela cell type", "TUMOR-SUPPRESSOR GENE, HELA CELL TYPE", "CERVICAL CARCINOMA, TUMOR-SUPPRESSOR GENE INVOLVED IN", "cervical carcinoma, tumor-suppressor Gene involved 1N"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "suppressor of tumorigenicity 3", "shortest_name_length": 3}
{"curie": "UMLS:C4520854", "names": ["stage I colorectal cancer", "Dukes A colorectal cancer", "Colorectal Cancer, Stage I", "Dukes A Colorectal Carcinoma", "Stage I Colorectal Carcinoma", "Stage I Colorectal Cancer AJCC v6", "Stage I Colorectal Cancer AJCC v7", "Stage I Colorectal Cancer AJCC v6 and v7", "Stage I Colorectal (Colon or Rectal) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Colorectal Cancer AJCC v6 and v7", "shortest_name_length": 25}
{"curie": "UMLS:C0435492", "names": ["sacrum fracture", "Sacral fracture", "Fracture;sacrum", "Sacrum fracture", "fracture sacrum", "Fractured sacrum", "fractured sacrum", "sacrum; fracture", "fracture; sacrum", "fractures sacrum", "Fracture of sacrum", "fracture of sacrum", "Sacral Spine Fracture", "Fracture of sacrum (disorder)", "fracture of sacrum (diagnosis)", "fracture; spine or vertebra, sacral", "spine or vertebra; fracture, sacral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fracture of sacrum", "shortest_name_length": 15}
{"curie": "UMLS:C1334025", "names": ["High Risk Gastric GIST", "High Risk Gastric Gastrointestinal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Risk Gastric Gastrointestinal Stromal Tumor", "shortest_name_length": 22}
{"curie": "MONDO:0005589", "names": ["thiopurine immunosuppressant-induced pancreatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thiopurine immunosuppressant-induced pancreatitis", "shortest_name_length": 49}
{"curie": "EFO:0009759", "names": ["Chronic Obstructive Asthma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic Obstructive Asthma", "shortest_name_length": 26}
{"curie": "MONDO:0011602", "names": ["DFNB27", "autosomal recessive deafness 27", "Deafness, Autosomal Recessive 27", "deafness, autosomal recessive 27", "DEAFNESS, AUTOSOMAL RECESSIVE 27", "autosomal recessive nonsyndromic deafness 27", "autosomal recessive nonsyndromic hearing loss 27", "autosomal recessive nonsyndromic deafness type 27"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 27", "shortest_name_length": 6}
{"curie": "MONDO:0014669", "names": ["CORD21", "cone-rod dystrophy 21", "CONE-ROD DYSTROPHY 21", "DRAM2 cone-rod dystrophy", "cone-rod dystrophy type 21", "cone-rod dystrophy caused by mutation in DRAM2", "retinal dystrophy with early macular involvement", "RETINAL DYSTROPHY WITH EARLY MACULAR INVOLVEMENT", "Retinal dystrophy with early macular involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cone-rod dystrophy 21", "shortest_name_length": 6}
{"curie": "UMLS:C2717957", "names": ["Vasoplegia", "Vasoplegias"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vasoplegia", "shortest_name_length": 10}
{"curie": "MONDO:0017077", "names": ["myelocystocele", "Myelocystocele", "Myelocystocele (disorder)", "Myelocystocele (diagnosis)", "congenital spinal anomaly spina bifida myelocystocele"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myelocystocele", "shortest_name_length": 14}
{"curie": "MONDO:0021097", "names": ["breast papilloma", "Breast papilloma", "Breast Papilloma", "Papilloma of Breast", "papilloma of breast", "Papilloma of breast", "breast duct papilloma", "Intracystic Papilloma", "Intracystic papilloma", "mammary duct papilloma", "ductal breast papilloma", "Ductal Breast Papilloma", "Papilloma of the Breast", "papilloma of the breast", "Duct papilloma of breast", "duct papilloma of breast", "Duct Papilloma of Breast", "Intraductal Papilloma, NOS", "duct papilloma of the breast", "Breast Intraductal Papilloma", "Duct Papilloma of the Breast", "intraductal breast papilloma", "Breast Intracystic Papilloma", "breast intraductal papilloma", "Intraductal Breast Papilloma", "intraductal papilloma breast", "Intracystic breast papilloma", "Intracystic papillary adenoma", "breast intraductal papillomas", "Intraduct papilloma of breast", "Papilloma of breast (disorder)", "BREAST, PAPILLOMA, INTRADUCTAL", "BREAST, PAPILLOMA, INTRACYSTIC", "Intraductal Papilloma of Breast", "papilloma of breast (diagnosis)", "Intraductal papilloma of breast", "intraductal papilloma of breast", "Duct papilloma of breast (disorder)", "intraductal papilloma of the breast", "Intraductal Papilloma of the Breast", "benign intraductal papilloma of breast", "Intraductal Papilloma, Not Otherwise Specified", "benign intraductal papilloma of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intraductal breast papilloma", "shortest_name_length": 16}
{"curie": "UMLS:C0036351", "names": ["Restzustand", "Schizophrenia residual", "residual schizophrenia", "RESIDUAL SCHIZOPHRENIA", "schizophrenia residual", "Residual schizophrenia", "schizophrenia; residual", "residual; schizophrenic", "schizophrenia; Restzustand", "Restzustand; schizophrenic", "Restzustand, schizophrenic", "Residual Type Schizophrenia", "SCHIZOPHRENIA RESIDUAL TYPE", "residual schizophrenia type", "Residual schizophrenia, NOS", "schizophrenia residual type", "residual type schizophrenia", "Restzustand (schizophrenic)", "schizophrenic residual state", "Schizophrenic residual state", "Schizophrenia, residual type", "Schizophrenia (Residual Type)", "state; residual schizophrenic", "residual schizophrenic; state", "Residual schizophrenia (disorder)", "residual schizophrenia (diagnosis)", "Residual type schizophrenic disorders", "Residual schizophrenia, unspecified state", "Schizophrenic disorders, residual type, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Residual schizophrenia", "shortest_name_length": 11}
{"curie": "UMLS:C4553617", "names": ["Stage IV Vaginal Cancer", "Stage IV Vaginal Cancer AJCC v8", "Stage IV Vaginal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Vaginal Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "MONDO:0012128", "names": ["DTGA", "D-TGA", "DTGA1", "TRANSPOSITION OF THE GREAT ARTERIES, DEXTRO-LOOPED", "transposition of the great arteries, dextro-looped", "dextro-looped transposition of the great arteries 1", "transposition of the great arteries, dextro-looped 1", "Transposition of the Great Arteries, Dextro-Looped 1", "dextro-looped transposition of the great arteries type 1", "MED13L dextro-looped transposition of the great arteries", "transposition of the great arteries, dextro-looped type 1", "dextro-looped transposition of the great arteries caused by mutation in MED13L"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transposition of the great arteries, dextro-looped", "shortest_name_length": 4}
{"curie": "MONDO:0006553", "names": ["Fox", "Fordyce-Fox", "apocrine miliaria", "miliaria apocrine", "Apocrine miliaria", "Apocrine Miliaria", "MILIARIA, APOCRINE", "miliaria, apocrine", "miliaria; apocrine", "Miliaria, Apocrine", "apocrine; miliaria", "fox fordyce disease", "FOX-FORDYCE DISEASE", "fordyce disease fox", "fox-fordyce disease", "Fox-Fordyce disease", "Fox-Fordyce Disease", "Fox Fordyce Disease", "Fox Fordyce disease", "Fox-Fordyce syndrome", "Fox Fordyce Syndrome", "Fox-Fordyce Syndrome", "Disease, Fox-Fordyce", "Syndrome, Fox-Fordyce", "Apocrine miliaria (disorder)", "Fox-Fordyce disease (diagnosis)", "Chronic itching papular eruption of axillae and pubes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fox-Fordyce disease", "shortest_name_length": 3}
{"curie": "UMLS:C0034214", "names": ["Pyogenic Granuloma of Skin and Subcutaneous Tissue", "Pyogenic granuloma of skin and subcutaneous tissue", "Lobular Capillary Hemangioma of Skin and Subcutaneous Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pyogenic granuloma of skin and subcutaneous tissue", "shortest_name_length": 50}
{"curie": "MONDO:0004905", "names": ["Deficiency;disaccharidase", "disaccharidase deficiency", "Disaccharidase deficiency", "disaccharidase; deficiency", "Disaccharide malabsorption", "deficiency; disaccharidase", "disaccharide; malabsorption", "malabsorption; disaccharide", "disaccharidase deficiencies", "Disaccharide malabsorption, NOS", "Disaccharide intolerance syndrome", "Disaccharidase deficiency syndrome", "Disaccharidase deficiency (disorder)", "Intestinal disaccharidase deficiency", "intestinal disaccharidase deficiency", "Intestinal disaccharidase deficiency, NOS", "Intestinal carbohydrate dyspepsia syndrome", "Intestinal disaccharidase deficiency (disorder)", "intestinal disaccharidase deficiency (diagnosis)", "intestinal disaccharide deficiency and disaccharide malabsorption", "Intestinal Disaccharidase Deficiency and Disaccharide Malabsorption", "intestinal disaccharidase deficiency and disaccharide malabsorption", "Intestinal disaccharidase deficiencies and disaccharide malabsorption"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intestinal disaccharidase deficiency", "shortest_name_length": 25}
{"curie": "MONDO:0016045", "names": ["46,XX/46,XY chimerism", "tetragametic chimerism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tetragametic chimerism", "shortest_name_length": 21}
{"curie": "MONDO:0004398", "names": ["mediastinal schwannoma", "Mediastinal Schwannoma", "mediastinum schwannoma", "mediastinal neurilemmoma", "Mediastinal Neurilemmoma", "Schwannoma of Mediastinum", "Schwannoma of mediastinum", "schwannoma of mediastinum", "neurilemmoma of mediastinum", "Neurilemmoma of Mediastinum", "benign mediastinal schwannoma", "schwannoma of the mediastinum", "Benign Mediastinal Schwannoma", "Schwannoma of the Mediastinum", "benign mediastinal neurilemmoma", "neurilemmoma of the mediastinum", "Neurilemmoma of the Mediastinum", "Benign Mediastinal Neurilemmoma", "benign schwannoma of mediastinum", "Benign Schwannoma of Mediastinum", "benign Schwannoma of mediastinum", "Benign Neurilemmoma of Mediastinum", "benign neurilemmoma of mediastinum", "Benign Schwannoma of the Mediastinum", "benign schwannoma of the mediastinum", "Benign Neurilemmoma of the Mediastinum", "benign neurilemmoma of the mediastinum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mediastinal schwannoma", "shortest_name_length": 22}
{"curie": "UMLS:C5206842", "names": ["Unresectable Malignant Digestive System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Malignant Digestive System Neoplasm", "shortest_name_length": 48}
{"curie": "MONDO:0007694", "names": ["HNT", "hairy nose tip", "HAIRY NOSE TIP", "Hairy nose tip"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hairy nose tip", "shortest_name_length": 3}
{"curie": "UMLS:C3888845", "names": ["Gastrointestinal mucosa hyperemia", "Gastrointestinal mucosa hyperaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal mucosa hyperemia", "shortest_name_length": 33}
{"curie": "UMLS:C0235462", "names": ["attack angina", "angina attack", "ANGINA ATTACK", "Angina attack", "angina attacks", "Anginal attack", "ANGINAL ATTACK", "anginal attack", "ANGINA EPISODE", "anginal attacks"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Angina attack", "shortest_name_length": 13}
{"curie": "UMLS:C0343960", "names": ["Generalized mucormycosis", "mucormycosis; generalized", "disseminated mucormycosis", "generalized; mucormycosis", "Disseminated mucormycosis", "mucormycosis; disseminated", "disseminated; mucormycosis", "Disseminated mucormycosis (disorder)", "disseminated mucormycosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disseminated mucormycosis", "shortest_name_length": 24}
{"curie": "MONDO:0011057", "names": ["cvd", "CVA", "stroke", "cerebral infarction", "brain; lesion, vascular", "CEREBROVASCULAR DISEASE", "Cerebrovascular Disease", "Brain Vascular Disorder", "lesion; cerebrovascular", "Cerebrovascular disease", "cerebrovascular; lesion", "cerebrovascular disease", "lesion; brain, vascular", "Disease;cerebrovascular", "cerebrovascular diseases", "cerebrovascular disorder", "Cerebrovascular diseases", "Cerebrovascular Diseases", "Cerebrovascular Disorder", "CEREBROVASCULAR DISEASES", "Cerebral vascular lesion", "CEREBROVASCULAR DISORDER", "Disorder cerebrovascular", "DISORDER CEREBROVASCULAR", "Brain Vascular Disorders", "Cerebrovascular disorder", "Disease, Cerebrovascular", "Vascular Disorder, Brain", "cerebrovascular accident", "CEREBRAL VASCULAR LESION", "cerebrovascular; disorder", "cerebrovascular disorders", "Diseases, Cerebrovascular", "Cerebrovascular Disorders", "Vascular Disorders, Brain", "cerebral vascular disorder", "Cerebrovascular lesion, NOS", "Cerebral Vascular Disorders", "cerebral vascular disorders", "Cerebrovascular disorder NOS", "Cerebrovascular disease, NOS", "Intracranial vascular disease", "Cerebral circulatory disorder", "CEREBRAL VASCULAR DISTURBANCE", "Cerebral vascular disturbance", "CVD - Cerebrovascular disease", "Intracranial Vascular Disease", "Vascular Disease, Intracranial", "CEREBRAL VASCULAR LESION (NOS)", "Intracranial Vascular Diseases", "Intracranial Vascular Disorder", "CEREBROVASCULAR DISORDER (NOS)", "Vascular Disorder, Intracranial", "Intracranial Vascular Disorders", "Vascular Diseases, Intracranial", "CVA (cerebral vascular accident)", "Vascular Disorders, Intracranial", "Cerebrovascular disease (disorder)", "Cerebrovascular diseases (I60-I69)", "CEREBRAL VASCULAR DISTURBANCE (NOS)", "cerebrovascular disease (diagnosis)", "Unspecified cerebrovascular disease", "Cerebrovascular disease, unspecified", "Cerebrovascular disease or lesion NOS", "disease (or disorder); cerebrovascular"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebrovascular disorder", "shortest_name_length": 3}
{"curie": "MONDO:0001136", "names": ["chylocele", "Chylocele", "CHYLOCELE", "Scrotal chylocele", "Chylocele (disorder)", "chylocele (diagnosis)", "chylocele; tunica vaginalis", "tunica vaginalis; chylocele", "Chylocele of tunica vaginalis", "chylocele of tunica vaginalis", "Chylocoele of tunica vaginalis", "chylocele of tunica vaginalis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chylocele of tunica vaginalis", "shortest_name_length": 9}
{"curie": "MONDO:0024461", "names": ["angiomatosis", "Angiomatosis", "Angiomatoses", "angiomatoses", "Angiomatosis, NOS", "diffuse hemangioma", "Diffuse Hemangioma", "Multiple Hemangiomas", "multiple hemangiomas", "Diffuse Angiomatosis", "diffuse angiomatosis", "Vascular Proliferation", "vascular proliferation", "Vascular proliferation", "Angiomatosis (disorder)", "Proliferation, vascular", "Angiomatosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angiomatosis", "shortest_name_length": 12}
{"curie": "MONDO:0013793", "names": ["ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNEL DEFICIENCY", "encephalomyopathy, mitochondrial, due to voltage-dependent anion channel deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephalomyopathy, mitochondrial, due to voltage-dependent anion channel deficiency", "shortest_name_length": 83}
{"curie": "MONDO:0014922", "names": ["MFM7", "myofibrillar myopathy 7", "myopathy, myofibrillar, 7", "MYOPATHY, MYOFIBRILLAR, 7", "myopathy, myofibrillar, type 7", "KY myofibrillar myopathy (disease)", "myofibrillar myopathy (disease) caused by mutation in KY", "alpha-b crystalin-related fatal infantile hypertonic myofibrillar myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myofibrillar myopathy 7", "shortest_name_length": 4}
{"curie": "MONDO:0007898", "names": ["Leukocyte Nuclear Appendages, Hereditary Prevalence of", "LEUKOCYTE NUCLEAR APPENDAGES, HEREDITARY PREVALENCE OF", "leukocyte nuclear appendages, hereditary prevalence of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukocyte nuclear appendages, hereditary prevalence of", "shortest_name_length": 54}
{"curie": "UMLS:C0333867", "names": ["Moderate cytologic atypia", "Moderate Cytologic Atypia", "Moderate cytologic atypia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Moderate cytologic atypia", "shortest_name_length": 25}
{"curie": "MONDO:0024327", "names": ["Chronic uremia", "uremia; chronic", "chronic; uremia", "Chronic uraemia", "Chronic uremia NOS", "Chronic Renal Failure", "chronic renal failure", "Chronic Renal Disease", "Chronic renal disease", "chronic kidney failure", "kidney failure, chronic", "Chronic renal impairment", "RENAL INSUFFICIENCY CHRONIC", "CRF - Chronic Renal Failure", "chronic renal insufficiency", "Chronic Renal Insufficiency", "Chronic renal insufficiency", "CRF - chronic renal failure", "chronic kidney insufficiency", "Renal Insufficiency, Chronic", "Chronic Kidney Insufficiency", "Kidney Insufficiency, Chronic", "insufficiency; renal, chronic", "Chronic Renal Insufficiencies", "chronic renal failure disease", "Chronic Kidney Insufficiencies", "kidney; insufficiency, chronic", "chronic renal failure syndrome", "Renal Insufficiencies, Chronic", "Kidney Insufficiencies, Chronic", "insufficiency; renal, end stage", "Chronic renal insufficiency (disorder)", "chronic renal insufficiency (diagnosis)", "insufficiency; renal, chronic, end stage renal disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic renal failure syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0006438", "names": ["Reichel Syndrome", "Reichels Syndrome", "Reichel's syndrome", "Reichel's Syndrome", "Syndrome, Reichel's", "Synovial Chondromatosis", "synovial chondromatosis", "Synovial chondromatosis", "Synovial Chondromatoses", "Henderson-Jones Syndrome", "Chondromatoses, Synovial", "Chondromatosis, Synovial", "Henderson Jones Syndrome", "Henderson-Jones syndrome", "Syndrome, Henderson-Jones", "Synovial Chondrometaplasia", "synovial chondrometaplasia", "Chondrometaplasia, Synovial", "Synovial Chondrometaplasias", "synovial osteochondromatosis", "Chondrometaplasias, Synovial", "synovial chondromatosis of joint", "Synovial chondromatosis (disorder)", "synovial chondromatosis of joint (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "synovial chondromatosis", "shortest_name_length": 16}
{"curie": "UMLS:C2267231", "names": ["CIN", "Idiopathic agranulocytosis", "chronic idiopathic neutropenia", "Chronic Idiopathic Neutropenia", "neutropenia chronic idiopathic", "Chronic idiopathic neutropenia", "idiopathic chronic neutropenia", "Chronic idiopathic neutropaenia", "Chronic idiopathic neutropenia (disorder)", "Chronic idiopathic neutropenia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic idiopathic neutropenia", "shortest_name_length": 3}
{"curie": "MONDO:0030428", "names": ["IMD85", "immunodeficiency 85 and autoimmunity", "IMMUNODEFICIENCY 85 AND AUTOIMMUNITY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 85 and autoimmunity", "shortest_name_length": 5}
{"curie": "MONDO:0014348", "names": ["MRT42", "GPIBD9", "NEDDSBA", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 42", "mental retardation, autosomal recessive 42", "mental retardation, autosomal recessive type 42", "intellectual disability, autosomal recessive 42", "glycosylphosphatidylinositol biosynthesis defect 9", "GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 9", "intellectual disability, autosomal recessive type 42", "PGAP1 autosomal recessive non-syndromic intellectual disability", "autosomal recessive non-syndromic intellectual disability caused by mutation in PGAP1", "neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities", "NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FEATURES, SPASTICITY, AND BRAIN ABNORMALITIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 42", "shortest_name_length": 5}
{"curie": "UMLS:C5447545", "names": ["Locally Advanced Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Lymphoma", "shortest_name_length": 25}
{"curie": "MONDO:0017881", "names": ["KFD", "KFD virus", "Monkey fever", "monkey fever", "Monkey disease", "monkey disease", "Kyasanur Forest Disease", "Kyasanur Forest disease", "Kyasanur forest disease", "Kyasanur hemorrhagic fever", "KF - Kyasanur Forest disease", "KFD - Kyasanur Forest disease", "Kyasanur Forest disease (disorder)", "Kyasanur forest disease (diagnosis)", "Kyasanur Forest Disease Virus Infection", "Kyasanur forest disease virus infectious disease", "Kyasanur forest disease virus disease or disorder", "Kyasanur forest disease virus caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kyasanur forest disease", "shortest_name_length": 3}
{"curie": "MONDO:0010412", "names": ["Craniofacioskeletal Syndrome", "CRANIOFACIOSKELETAL SYNDROME", "craniofacioskeletal syndrome", "X-linked intellectual disability-craniofacioskeletal syndrome", "craniofacioskeletal syndrome, X-linked recessive, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability-craniofacioskeletal syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0044782", "names": ["esophagus ulcer", "Esophageal Ulcer", "esophageal ulcer", "Esophageal ulcer", "esophagus ulcer disease", "ulcer disease of esophagus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophageal ulcer", "shortest_name_length": 15}
{"curie": "MONDO:0100268", "names": ["PEX14 related Zellweger spectrum disorder", "peroxisome biogenesis disorder due to PEX14 defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder due to PEX14 defect", "shortest_name_length": 41}
{"curie": "MONDO:0020577", "names": ["Gonadal Germ Cell Tumor", "Gonadal germ cell tumor", "Gonadal germ cell tumors", "Childhood Gonadal Germ Cell Tumor", "pediatric gonadal germ cell tumor", "childhood gonadal germ cell tumor", "gonadal germ cell tumor of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood gonadal germ cell tumor", "shortest_name_length": 23}
{"curie": "MONDO:0020183", "names": ["neurogenic palpebral tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurogenic palpebral tumor", "shortest_name_length": 26}
{"curie": "MONDO:0012149", "names": ["ADHD1", "attention deficit-hyperactivity disorder, susceptibility to, 1", "ATTENTION DEFICIT-HYPERACTIVITY DISORDER, SUSCEPTIBILITY TO, 1", "attention deficit-hyperactivity disorder, susceptibility to, type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "attention deficit-hyperactivity disorder, susceptibility to, 1", "shortest_name_length": 5}
{"curie": "MONDO:0002235", "names": ["eyelid tumor", "Eyelid Tumor", "EYELID TUMOR", "Eyelid tumor", "eyelid tumour", "eyelid cancer", "Eyelid tumour", "eyelid tumors", "Tumor of Eyelid", "eyelid neoplasm", "Tumor of eyelid", "palpebral tumor", "tumor of eyelid", "neoplasm eyelid", "Eyelid Neoplasm", "Eyelids--Tumors", "Tumour of eyelid", "Eyelid Neoplasms", "Neoplasm, Eyelid", "eyelid neoplasms", "Neoplasms, Eyelid", "Neoplasm of eyelid", "neoplasm of eyelid", "Neoplasm of Eyelid", "Skin cancer, eyelid", "tumor of the eyelid", "Tumor of the Eyelid", "Neoplasm of the Eyelid", "eyelid benign neoplasm", "neoplasm of the eyelid", "eyelid neoplasm (disease)", "Tumor of eyelid (disorder)", "neoplasm of eyelid (diagnosis)", "neoplasm of ocular adnexa eyelid", "tumor of eyelid (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eyelid neoplasm", "shortest_name_length": 12}
{"curie": "MONDO:0010674", "names": ["MPS2", "MPS 2", "MPSII", "MPS II", "severe MPS II", "Hunter disease", "I2S deficiency", "hunter disease", "IDS DEFICIENCY", "IDS deficiency", "HUNTER SYNDROME", "hunter syndrome", "SIDS DEFICIENCY", "disease hunters", "SIDS deficiency", "Hunter Syndrome", "Hunter syndrome", "Syndrome, Hunter", "syndrome; Hunter", "hunters syndrome", "Hunters Syndrome", "Hunter; syndrome", "diseases hunters", "Hunter's Syndrome", "Hunter's syndrome", "hunter's syndrome", "Syndrome, Hunter's", "Hunter-Fraser syndrome", "Mucopolysaccharidosis 2", "MUCOPOLYSACCHARIDOSIS II", "mucopolysaccharidosis ii", "X-linked Hurler syndrome", "Hunter-McAlpine syndrome", "MPS II - Hunter syndrome", "mucopolysaccharidosis II", "Mucopolysaccharidosis II", "MPS with skin involvement", "Hunter Syndrome Gargoylism", "Gargoylism, Hunter Syndrome", "mucopolysaccharidosis type 2", "Mucopolysaccharidosis Type 2", "Mucopolysaccharidosis type 2", "Mucopolysaccharidosis, MPS-II", "mucopolysaccharidosis, type 2", "mucopolysaccharidosis type ii", "Mucopolysaccharidosis Type II", "mucopolysaccharidosis, MPS-II", "Mucopolysaccharidosis type II", "mucopolysaccharidosis type II", "mucopolysaccharidosis (MPS) II", "mucopolysaccharidosis, type II", "mucopolysaccharidosis; type II", "MUCOPOLYSACCHARIDOSIS, TYPE II", "Mucopolysaccharidosis, type II", "iduronate sulfatase deficiency", "type II; mucopolysaccharidosis", "Iduronate sulfatase deficiency", "Iduronate sulphatase deficiency", "MPS 2 - Mucopolysaccharidosis 2", "IDURONATE 2-SULFATASE DEFICIENCY", "Iduronate 2-sulfatase deficiency", "iduronate 2-sulfatase deficiency", "Iduronate 2-sulphatase deficiency", "SULFOIDURONATE SULFATASE DEFICIENCY", "Deficiency of iduronate-2-sulfatase", "sulfoiduronate sulfatase deficiency", "deficiency of iduronate-2-sulphatase", "Deficiency of iduronate-2-sulphatase", "sulfo-iduronate sulfatase deficiency", "Sulfo-iduronate sulfatase deficiency", "iduronate sulfatase (IDS) deficiency", "Sulpho-iduronate sulfatase deficiency", "mucopolysaccharide storage disease II", "Sulfoiduronidate sulfatase deficiency", "MPSII - Mucopolysaccharidosis type II", "Sulpho-iduronate sulphatase deficiency", "Mucopolysaccharidosis, type II (MPS II)", "Sulphoiduronidate sulphatase deficiency", "Mucopolysaccharidosis type II (disorder)", "sulfo-iduronate sulfatase (SIDS) deficiency", "mucopolysaccharidosis with skin involvement", "mucopolysaccharidosis II, X-linked recessive", "mucopolysaccharidosis type II: Hunter syndrome", "attenuated MPS (subtype; formerly known as mild MPS II)", "mucopolysaccharidosis type II: Hunter syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucopolysaccharidosis type 2", "shortest_name_length": 4}
{"curie": "MONDO:0008313", "names": ["PVOP1", "vaginal hernia", "hernia vaginal", "rectal prolapse", "hernias vaginal", "vagina; prolapse", "VAGINAL PROLAPSE", "Vaginal Prolapse", "prolapse vaginal", "vaginal prolapse", "Vaginal prolapse", "Prolapse vaginal", "Vaginal Prolapses", "Prolapse, Vaginal", "Prolapses, Vaginal", "Vaginal prolapse NOS", "vaginal wall prolapse", "Vaginal prolapse, NOS", "Vaginal wall prolapse", "prolapse vaginal walls", "PROLAPSE OF VAGINA AND RECTUM", "prolapse of vagina and rectum", "Vaginal wall prolapse (disorder)", "vaginal wall prolapse (diagnosis)", "pelvic organ prolapse, susceptibility to", "PELVIC ORGAN PROLAPSE, SUSCEPTIBILITY TO", "pelvic organ prolapse, susceptibility to, 1", "PELVIC ORGAN PROLAPSE, SUSCEPTIBILITY TO, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pelvic organ prolapse, susceptibility to", "shortest_name_length": 5}
{"curie": "MONDO:0012049", "names": ["OFD7", "Ofds 7", "OFDS VII", "Whelan syndrome", "Whelan Syndrome", "WHELAN SYNDROME", "orofaciodigital syndrome 7", "OROFACIODIGITAL SYNDROME VII", "orofaciodigital syndrome VII", "Orofaciodigital Syndrome VII", "digito-orofacial syndrome VII", "orofaciodigital syndrome type 7", "oral-facial-digital syndrome VII", "orofaciodigital syndrome type VII", "orofaciodigital (OFD) syndrome VII", "oral-Facial-digital syndrome, type 7", "Oral-Facial-Digital Syndrome, Type VII", "ORAL-FACIAL-DIGITAL SYNDROME, TYPE VII"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orofaciodigital syndrome VII", "shortest_name_length": 4}
{"curie": "MONDO:0020772", "names": ["JAE1", "EJA1", "juvenile absence epilepsy 1", "epilepsy, juvenile absence, susceptibility to, 1", "EPILEPSY, JUVENILE ABSENCE, SUSCEPTIBILITY TO, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, juvenile absence, susceptibility to, 1", "shortest_name_length": 4}
{"curie": "UMLS:C0031570", "names": ["School phobia", "school phobia", "phobia school", "School Phobia", "school phobias", "Scolionophobia", "Phobia, School", "School phobia (finding)", "school phobia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Phobia, School", "shortest_name_length": 13}
{"curie": "MONDO:0008296", "names": ["PCT", "PCT, type 2", "PCT, type II", "PCT, TYPE II", "Urod deficiency", "UROD DEFICIENCY", "UROD deficiency", "PCT, 'familial' type", "PCT, 'FAMILIAL' TYPE", "porphyria cutanea tarda", "Porphyria cutanea tarda type II", "porphyria, hepatoerythropoietic", "porphyria, Hepatocutaneous type", "porphyria cutanea tarda type II", "porphyria cutanea tarda, type 2", "Familial porphyria cutanea tarda", "familial porphyria cutanea tarda", "PORPHYRIA CUTANEA TARDA, TYPE II", "Porphyria cutanea tarda, familial", "Hereditary porphyria cutanea tarda", "hereditary porphyria cutanea tarda", "UROPORPHYRINOGEN DECARBOXYLASE DEFICIENCY", "uroporphyrinogen decarboxylase deficiency", "Uroporphyrinogen decarboxylase deficiency", "porphyria cutanea tarda, susceptibility to", "Familial porphyria cutanea tarda (disorder)", "Uroporphyrinogen decarboxylase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial porphyria cutanea tarda", "shortest_name_length": 3}
{"curie": "MONDO:0011746", "names": ["Symphalangism, distal, with microdontia, dental pulp stones, and narrowed zygomatic arch", "symphalangism, distal, with microdontia, dental pulp stones, and narrowed zygomatic arch", "SYMPHALANGISM, DISTAL, WITH MICRODONTIA, DENTAL PULP STONES, AND NARROWED ZYGOMATIC ARCH", "Distal symphalangism, hypoplastic carpal bones, microdontia, dental pulp stones, and narrowing of the zygomatic arch", "distal symphalangism, hypoplastic carpal bones, microdontia, dental pulp stones, and narrowing of the zygomatic arch"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "symphalangism, distal, with microdontia, dental pulp stones, and narrowed zygomatic arch", "shortest_name_length": 88}
{"curie": "UMLS:C4763846", "names": ["Metastatic Genitourinary Tumor", "Metastatic Malignant Genitourinary System Neoplasm", "Metastatic Genitourinary System Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Malignant Genitourinary System Neoplasm", "shortest_name_length": 30}
{"curie": "MONDO:0044299", "names": ["CMS22", "PREPL DEFICIENCY", "Prepl deficiency", "congenital myasthenic syndrome 22", "myasthenic syndrome, congenital, 22", "MYASTHENIC SYNDROME, CONGENITAL, 22"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myasthenic syndrome, congenital, 22", "shortest_name_length": 5}
{"curie": "MONDO:0019083", "names": ["Leigh disease with myopathy", "Leigh syndrome with cardiomyopathy", "cardiomyopathy with myopathy due to COX deficiency", "cardiomyopathy with hypotonia due to cytochrome C oxidase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leigh syndrome with cardiomyopathy", "shortest_name_length": 27}
{"curie": "UMLS:C5206592", "names": ["Epididymal Melanotic Neuroectodermal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epididymal Melanotic Neuroectodermal Tumor", "shortest_name_length": 42}
{"curie": "UMLS:C0340116", "names": ["Skin Lymphangioleiomyomatosis", "Lymphangioleiomyomatosis of skin", "Lymphangioleiomyomatosis of Skin", "Lymphangioleiomyomatosis of the Skin", "Lymphangioleiomyomatosis of skin (disorder)", "Lymphangioleiomyomatosis of skin (diagnosis)", "skin neoplasm uncertain behavior lymphangioleiomyomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphangioleiomyomatosis of skin", "shortest_name_length": 29}
{"curie": "MONDO:0700074", "names": ["GA2B", "ETFB deficiency", "glutaric acidemia 2B", "glutaric acidemia IIb", "multiple acyl-CoA dehydrogenase deficiency caused by mutation in ETFB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glutaric acidemia IIb", "shortest_name_length": 4}
{"curie": "MONDO:0021181", "names": ["Inherited Coagulation Disorder", "inherited coagulation disorder", "inherited coagulation disorders", "coagulation disorder, inherited", "hereditary coagulation disorder", "Hereditary Coagulation Disorder", "Coagulation Disorder, Inherited", "Inherited Coagulation Disorders", "Hereditary Coagulation Disorders", "Coagulation Disorders, Inherited", "Coagulation disorders congenital", "coagulation disorder, hereditary", "hereditary coagulation disorders", "Coagulation Disorder, Hereditary", "coagulation disorders, inherited", "coagulation disorders, hereditary", "rare genetic coagulation disorder", "Coagulation Disorders, Hereditary", "inherited blood coagulation disease", "hereditary blood coagulation disease", "inherited blood coagulation disorder", "inherited blood coagulation disorders", "Inherited Blood Coagulation Disorders", "hereditary blood coagulation disorders", "Blood Coagulation Disorders, Inherited", "Hereditary Blood Coagulation Disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited blood coagulation disorder", "shortest_name_length": 30}
{"curie": "UMLS:C1692321", "names": ["INFILTRATE", "Infiltration", "cellular infiltrate", "Cellular infiltrate", "Cellular Infiltrate", "Infiltration (N/F/D)", "Cellular Infiltration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cellular infiltrate", "shortest_name_length": 10}
{"curie": "MONDO:0017571", "names": ["Proteus-like syndrome", "PROTEUS-LIKE SYNDROME", "Proteus-Like Syndrome", "Proteus Like Syndrome", "Proteus like syndrome", "Cohen-Hayden syndrome", "Syndrome, Proteus-Like", "Proteus-Like Syndrome (disorder)", "Proteus like syndrome (disorder)", "Proteus like syndrome mental retardation eye defect", "Proteus like syndrome intellectual disability eye defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Proteus-like syndrome", "shortest_name_length": 21}
{"curie": "MONDO:0013576", "names": ["IGKCD", "kappa chain deficiency", "Kappa-Chain Deficiency", "Kappa-chain deficiency", "kappa-chain deficiency", "KAPPA CHAIN DEFICIENCY", "kappa light chain deficiency", "isolated IgG subclass deficiency", "Isolated IgG subclass deficiency", "Selective IgG subclass deficiency", "selective IgG subclass deficiency", "IMMUNOGLOBULIN KAPPA LIGHT CHAIN DEFICIENCY", "IMMUNOGLOBULIN kappa LIGHT chain deficiency", "Immunoglobulin kappa light chain deficiency", "IgG subclass deficiency with IgA subclass deficiency", "Recurrent infections associated with rare immunoglobulin isotypes deficiency", "recurrent infections associated with rare immunoglobulin isotypes deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "recurrent infections associated with rare immunoglobulin isotypes deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0005432", "names": ["alcohol and nicotine codependence"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alcohol and nicotine codependence", "shortest_name_length": 33}
{"curie": "MONDO:0005297", "names": ["ngu", "NGU", "NGU, NOS", "URETHRITIS", "urethritis", "Urethritis", "Urethritides", "Urethritis NOS", "Urethritis, NOS", "urethra inflammation", "urethritis (disease)", "Urethritis (disorder)", "Urethral inflammation", "Urethritis nonspecific", "Nonspecific urethritis", "urethritis (diagnosis)", "nonspecific urethritis", "NONSPECIFIC URETHRITIS", "Nonvenereal urethritis", "urethritis nonspecific", "nonspecific; urethritis", "non specific urethritis", "Urethritis, unspecified", "Urethritis non specific", "Inflammation of urethra", "Urethritis-non-specific", "inflammation of urethra", "Non-venereal urethritis", "urethritis; nonspecific", "Urethritis non-specific", "non-specific urethritis", "URETHRITIS NONGONOCOCCAL", "Nongonococcal urethritis", "nongonococcal urethritis", "NONGONOCOCCAL URETHRITIS", "non-gonococcal urethritis", "urethritis; nongonococcal", "Non-gonococcal urethritis", "Non-Gonococcal Urethritis", "Nonspecific urethritis, NOS", "NSU - Nonspecific urethritis", "Nonspecific urethritis (NSU)", "Nongonococcal urethritis, NOS", "Nonspecific genital infection", "NGU (nongonococcal urethritis)", "Non-gonococcal urethritis (NGU)", "NGU - Non-gonococcal urethritis", "non-gonococcal urethritis (NGU)", "urethritis nonspecific (diagnosis)", "Nongonococcal urethritis (disorder)", "NSGI - Nonspecific genital infection", "nongonococcal urethritis (diagnosis)", "Unspecified non-gonococcal urethritis (NGU)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urethritis", "shortest_name_length": 3}
{"curie": "MONDO:0016387", "names": ["OXPHOS disease", "OXPHOS system deficiency", "mitochondrial oxidative phosphorylation disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial oxidative phosphorylation disorder", "shortest_name_length": 14}
{"curie": "UMLS:C4528176", "names": ["High Risk Myelodysplastic Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Risk Myelodysplastic Syndrome", "shortest_name_length": 34}
{"curie": "MONDO:0014314", "names": ["SAVA", "SACRAL AGENESIS WITH VERTEBRAL ANOMALIES", "sacral agenesis with vertebral anomalies", "sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C5555954", "names": ["Broad Ligament Ependymoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Broad Ligament Ependymoma", "shortest_name_length": 25}
{"curie": "MONDO:0016502", "names": ["HPS without pulmonary fibrosis", "Hermansky-Pudlak syndrome without pulmonary fibrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hermansky-Pudlak syndrome without pulmonary fibrosis", "shortest_name_length": 30}
{"curie": "UMLS:C2981177", "names": ["Stage II Penile Cancer", "Stage II Penis Cancer AJCC v6", "Penile Cancer Stage II AJCC v6", "Stage II Penile Cancer AJCC v6", "Stage II Penis Carcinoma AJCC v6", "Stage II Penile Carcinoma AJCC v6", "Penile Carcinoma Stage II AJCC v6", "Stage II Carcinoma of Penis AJCC v6", "Stage II Carcinoma of the Penis AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Penile Cancer AJCC v6", "shortest_name_length": 22}
{"curie": "MONDO:0003460", "names": ["clear cell adenofibroma", "Clear cell adenofibroma", "Clear Cell Adenofibroma", "clear cell adenofibroma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "clear cell adenofibroma", "shortest_name_length": 23}
{"curie": "UMLS:C3146271", "names": ["Stage III Breast Cancer", "Stage III Breast Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Breast Cancer AJCC v7", "shortest_name_length": 23}
{"curie": "MONDO:0011610", "names": ["DMGDHD", "DMGDH Deficiency", "Dmgdh deficiency", "DMGDH deficiency", "DMGDH DEFICIENCY", "DMG dehydrogenase deficiency", "Dimethylglycine Dehydrogenase Deficiency", "DIMETHYLGLYCINE DEHYDROGENASE DEFICIENCY", "dimethylglycine dehydrogenase deficiency", "Dimethylglycine dehydrogenase deficiency", "Deficiency of dimethylglycine dehydrogenase", "dimethylglycine dehydrogenase activity disease", "disorder of dimethylglycine dehydrogenase activity", "Deficiency of dimethylglycine dehydrogenase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dimethylglycine dehydrogenase deficiency", "shortest_name_length": 6}
{"curie": "UMLS:C0152156", "names": ["dystocia", "obstructed labor", "Obstructed labor", "Obstructed Labor", "Labour;obstructed", "Obstructed labour", "labor, obstructed", "obstructed labour", "Labor, obstructed", "Obstructed labor NOS", "delivery; obstruction", "obstruction; delivery", "Obstructed labour NOS", "Obstructed labor, NOS", "Obstructed labour, NOS", "Obstructed labor (disorder)", "obstructed labor (diagnosis)", "Unspecified obstructed labor", "Unspecified obstructed labour", "Obstructed labor, unspecified", "Obstructed labour, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Obstructed labor", "shortest_name_length": 8}
{"curie": "MONDO:0007397", "names": ["CMD", "CMDD", "CMDJ", "craniometaphyseal dysplasia Jackson type", "Craniometaphyseal dysplasia Jackson type", "craniometaphyseal dysplasia, Jackson type", "Craniometaphyseal dysplasia dominant type", "CRANIOMETAPHYSEAL DYSPLASIA, JACKSON TYPE", "Craniometaphyseal Dysplasia, Jackson Type", "autosomal dominant craniometaphyseal dysplasia", "Craniometaphyseal dysplasia autosomal dominant", "Autosomal Dominant Craniometaphyseal Dysplasia", "Craniometaphyseal Dysplasia, Autosomal Dominant", "CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT", "craniometaphyseal dysplasia, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniometaphyseal dysplasia, autosomal dominant", "shortest_name_length": 3}
{"curie": "MONDO:0015520", "names": ["late infantile CACH syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "late infantile CACH syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0001972", "names": ["Brucella melitensis", "Caprine brucellosis", "melitensis; brucellosis", "brucellosis; melitensis", "Brucella melitensis infection", "infection; Brucella, melitensis", "Brucella; infection, melitensis", "Brucella melitensis brucellosis", "Infection due to Brucella melitensis", "infection due to Brucella melitensis", "Brucellosis due to Brucella melitensis", "Infection caused by Brucella melitensis", "infection due to Brucella melitensis (diagnosis)", "Infection caused by Brucella melitensis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brucella melitensis brucellosis", "shortest_name_length": 19}
{"curie": "MONDO:0017564", "names": ["macrodactyly of hand, unilateral", "macrodactyly of fingers, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macrodactyly of fingers, unilateral", "shortest_name_length": 32}
{"curie": "MONDO:0002583", "names": ["ovary mucinous cystadenoma", "ovarian mucinous cystadenoma", "Ovarian Mucinous Cystadenoma", "mucinous ovarian cystadenoma", "Ovarian mucinous Cystadenoma", "Mucinous cystadenoma of ovary", "Mucinous Cystadenoma of Ovary", "mucinous cystadenoma of ovary", "mucinous cystadenoma of the ovary", "Mucinous Cystadenoma of the Ovary", "benign ovarian mucinous cystadenoma", "Benign Ovarian Mucinous Cystadenoma", "benign mucinous cystadenoma of ovary", "Benign Mucinous Cystadenoma of Ovary", "Benign Mucinous Cystadenoma of the Ovary", "benign mucinous cystadenoma of the ovary", "Mucinous cystadenoma of ovary (disorder)", "mucinous cystadenoma of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucinous ovarian cystadenoma", "shortest_name_length": 26}
{"curie": "MONDO:0032588", "names": ["PVNH8", "PERIVENTRICULAR NODULAR HETEROTOPIA 8", "periventricular nodular heterotopia 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "periventricular nodular heterotopia 8", "shortest_name_length": 5}
{"curie": "UMLS:C1096708", "names": ["Venipuncture site inflammation", "Vessel puncture site inflammation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vessel puncture site inflammation", "shortest_name_length": 30}
{"curie": "UMLS:C4721793", "names": ["Ovarian Cancer Stage IIB", "Stage IIB Ovarian Cancer", "FIGO Stage IIB Ovarian Cancer", "AJCC Stage IIB Ovarian Cancer", "FIGO Stage IIB Cancer of Ovary", "Stage IIB Ovarian Cancer AJCC v7", "Stage IIB Ovarian Cancer AJCC v6", "FIGO Stage IIB Ovarian Carcinoma", "FIGO Stage IIB Carcinoma of Ovary", "FIGO Stage IIB Cancer of the Ovary", "Stage IIB Ovarian Epithelial Cancer", "FIGO Stage IIB Carcinoma of the Ovary", "Stage IIB Ovarian Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Ovarian Cancer AJCC v6 and v7", "shortest_name_length": 24}
{"curie": "MONDO:0013312", "names": ["RP55", "retinitis pigmentosa 55", "RETINITIS PIGMENTOSA 55", "ARL6 retinitis pigmentosa", "retinitis pigmentosa type 55", "retinitis pigmentosa caused by mutation in ARL6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 55", "shortest_name_length": 4}
{"curie": "MONDO:0035736", "names": ["AHB", "acquired hemophilia B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired hemophilia B", "shortest_name_length": 3}
{"curie": "MONDO:0012934", "names": ["CLLS3", "Clls3", "leukemia, chronic lymphocytic, susceptibility to, 3", "LEUKEMIA, CHRONIC LYMPHOCYTIC, SUSCEPTIBILITY TO, 3", "leukemia, chronic lymphocytic, susceptibility to, type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukemia, chronic lymphocytic, susceptibility to, 3", "shortest_name_length": 5}
{"curie": "UMLS:C1336176", "names": ["Stage IIB Bladder Cancer", "Stage IIB Urinary Bladder Cancer", "Stage IIB Urinary Bladder Carcinoma", "Jewett-Marshall Stage B2 Bladder Cancer", "Jewett-Marshall Stage B2 Bladder Carcinoma", "Jewett-Marshall Stage B2 Urinary Bladder Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Bladder Cancer", "shortest_name_length": 24}
{"curie": "MONDO:0012254", "names": ["Multiple epiphyseal dysplasia with miniepiphyses", "multiple epiphyseal dysplasia with miniepiphyses", "multiple epiphyseal dysplasia, with miniepiphyses", "Multiple epiphyseal dysplasia, with miniepiphyses", "Epiphyseal Dysplasia, Multiple, with Miniepiphyses", "EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MINIEPIPHYSES", "epiphyseal dysplasia, multiple, with miniepiphyses", "Multiple epiphyseal dysplasia with miniepiphyses (disorder)", "multiple epiphyseal dysplasia with miniepiphyses (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple epiphyseal dysplasia, with miniepiphyses", "shortest_name_length": 48}
{"curie": "MONDO:0013219", "names": ["ARHR2", "hypophosphatemic rickets, autosomal recessive, 2", "HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL RECESSIVE, 2", "Hypophosphatemic Rickets, Autosomal Recessive, 2", "ENPP1 autosomal recessive hypophosphatemic rickets", "hypophosphatemic rickets, autosomal recessive, type 2", "autosomal recessive hypophosphatemic rickets caused by mutation in ENPP1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypophosphatemic rickets, autosomal recessive, 2", "shortest_name_length": 5}
{"curie": "UMLS:C5205645", "names": ["Recurrent Anaplastic Pleomorphic Xanthoastrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Anaplastic Pleomorphic Xanthoastrocytoma", "shortest_name_length": 50}
{"curie": "UMLS:C1335712", "names": ["Relapsed Medulloblastoma", "Recurrent Medulloblastoma", "Medulloblastoma recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Medulloblastoma", "shortest_name_length": 24}
{"curie": "UMLS:C0155749", "names": ["Arterial embolus and thrombosis", "arterial embolus and thrombosis", "Arterial embolism and thrombosis", "Arterial embolic and thrombotic occlusion", "Arterial embolus and thrombosis (disorder)", "arterial embolus and thrombosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arterial embolus and thrombosis", "shortest_name_length": 31}
{"curie": "MONDO:0035345", "names": ["CBE", "KSD", "BIND", "Kernicterus spectrum disorder", "chronic bilirubin encephalopathy", "Bilirubin-induced neurological dysfunction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic bilirubin encephalopathy", "shortest_name_length": 3}
{"curie": "MONDO:0003706", "names": ["adult brainstem astrocytoma", "Adult Brainstem Astrocytoma", "Adult Brain Stem Astrocytoma", "adult brain stem astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult brainstem astrocytoma", "shortest_name_length": 27}
{"curie": "UMLS:C0919714", "names": ["Retinal vascular thrombosis", "Retinal vascular thrombosis NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retinal vascular thrombosis", "shortest_name_length": 27}
{"curie": "MONDO:0002904", "names": ["Echolalia", "echolalia", "Echologia", "ECHOLALIA", "Echo speech", "echo speech", "Echophrasia", "Echo Speech", "Speech, Echo", "Echo Reaction", "Reaction, Echo", "Reactions, Echo", "Repeated speech", "echolalia (disease)", "Echolalia (finding)", "Echoing another person's speech"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "echolalia", "shortest_name_length": 9}
{"curie": "UMLS:C5419896", "names": ["EBV-Positive Inflammatory Follicular Dendritic Cell Sarcoma", "Epstein-Barr Virus Positive Inflammatory Follicular Dendritic Cell Sarcoma", "Epstein-Barr Virus-Positive Inflammatory Follicular Dendritic Cell Sarcoma", "Inflammatory Pseudotumor-Like Follicular/Fibroblastic Dendritic Cell Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "EBV-Positive Inflammatory Follicular Dendritic Cell Sarcoma", "shortest_name_length": 59}
{"curie": "MONDO:0014090", "names": ["PAPA6", "polydactyly, postaxial, type A6", "POLYDACTYLY, POSTAXIAL, TYPE A6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polydactyly, postaxial, type A6", "shortest_name_length": 5}
{"curie": "UMLS:C1708996", "names": ["Metastatic Extraosseous Myxoid Chondrosarcoma", "Metastatic Extraskeletal Myxoid Chondrosarcoma", "Extraskeletal Myxoid Chondrosarcoma, Metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Extraskeletal Myxoid Chondrosarcoma", "shortest_name_length": 45}
{"curie": "UMLS:C0035085", "names": ["Renal Infarct", "renal infarct", "Renal infarct", "infarct renal", "Kidney Infarct", "Renal infarction", "RENAL INFARCTION", "renal infarction", "infarction kidney", "renal; infarction", "kidney infarction", "infarction; renal", "kidney; infarction", "infarction; kidney", "KIDNEY, INFARCTION", "Infarction of kidney", "Renal infarction (disorder)", "renal infarction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal infarction", "shortest_name_length": 13}
{"curie": "UMLS:C1707251", "names": ["Other cancer", "Other Cancer", "Cancer Other", "Other Malignancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cancer Other", "shortest_name_length": 12}
{"curie": "MONDO:0003219", "names": ["adenocarcinoma - GEJ", "Adenocarcinoma - GEJ", "esophagogastric adenocarcinoma", "adenocarcinoma of the EG junction", "Adenocarcinoma of the EG Junction", "adenocarcinoma of the GE junction", "Adenocarcinoma of the GE Junction", "esophagogastric junction adenocarcinoma", "gastroesophageal junction adenocarcinoma", "Gastroesophageal junction adenocarcinoma", "Gastroesophageal Junction Adenocarcinoma", "adenocarcinoma of esophagogastric junction", "adenocarcinoma of Cardioesophageal junction", "Adenocarcinoma of Cardioesophageal Junction", "adenocarcinoma of cardioesophageal junction", "Adenocarcinoma of Gastroesophageal Junction", "Adenocarcinoma of Cardioesophageal junction", "adenocarcinoma of gastroesophageal junction", "Adenocarcinoma of the Esophagogastric Junction", "adenocarcinoma of the esophagogastric junction", "Adenocarcinoma of the Cardioesophageal Junction", "Adenocarcinoma of the Gastroesophageal Junction", "Adenocarcinoma of the gastroesophageal junction", "adenocarcinoma of the cardioesophageal junction", "Adenocarcinoma of the Cardioesophageal junction", "adenocarcinoma of the gastroesophageal junction", "Adenocarcinoma of the gastrooesophageal junction", "adenocarcinoma of esophagogastric junction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastroesophageal junction adenocarcinoma", "shortest_name_length": 20}
{"curie": "MONDO:0006349", "names": ["papillary cystic tumor", "Solid and cystic tumor", "Papillary Cystic Tumor", "Papillary cystic tumor", "tumor; papillary cystic", "Papillary cystic tumour", "Solid and cystic tumour", "papillary; tumor, cystic", "papillary cystic neoplasm", "Papillary Cystic Neoplasm", "[M] Papillary cystic tumor", "[M] Papillary cystic tumour", "Solid and papillary epithelial neoplasm", "Papillary cystic tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papillary cystic neoplasm", "shortest_name_length": 22}
{"curie": "UMLS:C0038187", "names": ["starvation", "Starvation", "STARVATION", "[X]Starvation", "Starvation, NOS", "Starvation (disorder)", "starvation (diagnosis)", "Starvation due to lack of food"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Starvation", "shortest_name_length": 10}
{"curie": "UMLS:C1336085", "names": ["Nasopharynx Papilloma", "Papilloma of Nasopharynx", "Nasopharyngeal Papilloma", "Papilloma of the Nasopharynx", "Squamous Papilloma of Nasopharynx", "Nasopharyngeal Squamous Papilloma", "Squamous Papilloma of the Nasopharynx", "Nasopharyngeal Squamous Cell Papilloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasopharyngeal Squamous Cell Papilloma", "shortest_name_length": 21}
{"curie": "MONDO:0022578", "names": ["Bladder Cancer", "bladder cancer", "childhood bladder cancer", "bladder cancer childhood", "bladder cancer, childhood", "childhood bladder carcinoma", "Childhood Bladder Carcinoma", "bladder carcinoma, childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood bladder carcinoma", "shortest_name_length": 14}
{"curie": "MONDO:0009307", "names": ["granulomatous disease with defect in neutrophil chemotaxis", "Granulomatous Disease with Defect in Neutrophil Chemotaxis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "granulomatous disease with defect in neutrophil chemotaxis", "shortest_name_length": 58}
{"curie": "MONDO:0007836", "names": ["IVIC", "OORS", "IVIC SYNDROME", "IVIC syndrome", "OCULOOTORADIAL SYNDROME", "Oculootoradial syndrome", "oculootoradial syndrome", "oculo-oto-radial syndrome", "Oculo-oto-radial syndrome", "Oculootoradial syndrome (disorder)", "Instituto Venezolano de Investigaciones Cientificas syndrome", "Instituto venezolano de Investigaciones Cientificas syndrome", "IVIC (Instituto Venezolano de Investigaciones Cientificas) syndrome", "RADIAL RAY DEFECTS, HEARING IMPAIRMENT, EXTERNAL OPHTHALMOPLEGIA, AND THROMBOCYTOPENIA", "Radial ray defects, hearing impairment, external ophthalmoplegia, and thrombocytopenia", "radial ray defects, hearing impairment, external ophthalmoplegia, and thrombocytopenia", "radial Ray defects, hearing impairment, external ophthalmoplegia, and thrombocytopenia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IVIC syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C4525693", "names": ["Stage I Appendix Neuroendocrine Tumor", "Stage I Appendix Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Appendix Neuroendocrine Tumor AJCC v8", "shortest_name_length": 37}
{"curie": "MONDO:0020256", "names": ["congenital CNIV palsy", "congenital trochlear nerve palsy", "congenital superior oblique palsy", "congenital fourth cranial nerve palsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital trochlear nerve palsy", "shortest_name_length": 21}
{"curie": "MONDO:0030553", "names": ["AMD4", "ACROMESOMELIC DYSPLASIA 4", "acromesomelic dysplasia-4", "acromesomelic dysplasia 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acromesomelic dysplasia 4", "shortest_name_length": 4}
{"curie": "UMLS:C4055194", "names": ["Cytomegalovirus Associated Congenital Nephrotic Syndrome", "Congenital Nephrotic Syndrome - Cytomegalovirus Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Nephrotic Syndrome - Cytomegalovirus Associated", "shortest_name_length": 56}
{"curie": "MONDO:0016563", "names": ["PSP-CBS", "PSP-corticobasal syndrome", "progressive supranuclear palsy-corticobasal syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive supranuclear palsy-corticobasal syndrome", "shortest_name_length": 7}
{"curie": "MONDO:0014183", "names": ["MYP23", "MYOPIA 23, AUTOSOMAL RECESSIVE", "myopia 23, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopia 23, autosomal recessive", "shortest_name_length": 5}
{"curie": "UMLS:C3695318", "names": ["Hypertensive chronic kidney disease", "hypertensive chronic kidney disease", "Hypertensive chronic kidney disease NOS", "Chronic Kidney Disease due to Hypertension", "Chronic kidney disease due to hypertension", "hypertensive chronic kidney disease (diagnosis)", "Chronic kidney disease due to hypertension (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic kidney disease due to hypertension", "shortest_name_length": 35}
{"curie": "UMLS:C1707552", "names": ["Cutaneous Mature T-Cell and NK-Cell Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous Mature T-Cell and NK-Cell Neoplasm", "shortest_name_length": 44}
{"curie": "MONDO:0033546", "names": ["NERIB", "SMVTD", "Smvt Deficiency", "SMVT DEFICIENCY", "Sodium-Dependent Multivitamin Transporter Deficiency", "SODIUM-DEPENDENT MULTIVITAMIN TRANSPORTER DEFICIENCY", "NEURODEGENERATION, INFANTILE-ONSET, BIOTIN-RESPONSIVE", "neurodegeneration, infantile-onset, biotin-responsive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodegeneration, infantile-onset, biotin-responsive", "shortest_name_length": 5}
{"curie": "MONDO:0018601", "names": ["autosomal dominant myopia-midfacial retrusion-sensorineural hearing loss-rhizomelic dysplasia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant myopia-midfacial retrusion-sensorineural hearing loss-rhizomelic dysplasia syndrome", "shortest_name_length": 102}
{"curie": "MONDO:0011928", "names": ["dipygus", "Dipygus", "Caudal duplication", "caudal duplication", "Dipygus (disorder)", "Duplication, caudal", "split notochord syndrome", "Split notochord syndrome", "caudal DUPLICATION anomaly", "CAUDAL DUPLICATION ANOMALY", "Caudal Duplication Anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "caudal duplication", "shortest_name_length": 7}
{"curie": "UMLS:C5575351", "names": ["EMD", "Extramedullary Disease", "Extramedullary Disease in Multiple Myeloma", "Extramedullary Disease in Plasma Cell Myeloma", "Extramedullary Manifestation in Multiple Myeloma", "Extramedullary Manifestation in Plasma Cell Myeloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extramedullary Disease in Plasma Cell Myeloma", "shortest_name_length": 3}
{"curie": "MONDO:0004597", "names": ["lung infarct", "lung infarction", "Infarct of lung", "lung; infarction", "infarction; lung", "Pulmonary infarct", "pulmonary infarct", "INFARCT PULMONARY", "PULMONARY INFARCT", "Pulmonary Infarct", "Infarct pulmonary", "Infarct, Pulmonary", "infarcts pulmonary", "Pulmonary Infarcts", "Infarcts, Pulmonary", "pulmonary infarction", "Pulmonary infarction", "Infarction;pulmonary", "Pulmonary Infarction", "infarction pulmonary", "PULMONARY INFARCTION", "Pulmonary Infarctions", "infarction, pulmonary", "Infarction, Pulmonary", "pulmonary; infarction", "pulmonary infarctions", "infarction; pulmonary", "Infarctions, Pulmonary", "Pulmonary infarction (disorder)", "pulmonary infarction (diagnosis)", "Pulmonary embolism and infarction", "pulmonary embolism and infarction", "Pulmonary embolism with infarction", "Pulmonary Embolism with Infarction", "pulmonary embolism with pulmonary infarction", "Pulmonary embolism with pulmonary infarction", "Pulmonary embolism with pulmonary infarction (disorder)", "pulmonary embolism with pulmonary infarction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary embolism and infarction", "shortest_name_length": 12}
{"curie": "UMLS:C4315240", "names": ["AVN_JOINT", "Avascular joint necrosis", "Avascular Necrosis of the Joint"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Avascular joint necrosis", "shortest_name_length": 9}
{"curie": "UMLS:C0262428", "names": ["COLLAGEN VASCULAR DISEASE", "collagen vascular disease", "vascular disease collagen", "COLLAGEN/VASCULAR DISEASE", "collagen-vascular disease", "collagen disease vascular", "Collagen-vascular disease", "vascular collagen disease", "collagen diseases vascular", "collagen vascular diseases", "collagen (vascular) disease NOS", "Collagen (vascular) disease NOS", "collagen vascular disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Collagen-vascular disease", "shortest_name_length": 25}
{"curie": "MONDO:0024651", "names": ["Osteoporosis due to corticosteroid", "osteoporosis due to corticosteroid", "corticosteroid-induced osteoporosis", "Osteoporosis caused by corticosteroid", "osteoporosis caused by corticosteroid", "Osteoporosis caused by corticosteroid (disorder)", "Osteoporosis caused by corticosteroid (diagnosis)", "osteoporosis drug-induced caused by corticosteroid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corticosteroid-induced osteoporosis", "shortest_name_length": 34}
{"curie": "UMLS:C0278767", "names": ["stage I CLL", "CLL Stage I", "Stage I CLL", "CLL, stage I", "Stage I Chronic Lymphocytic Leukemia", "Chronic Lymphocytic Leukemia Stage I", "stage I chronic lymphocytic leukemia", "Chronic lymphocytic leukemia stage 1", "chronic lymphocytic leukemia, stage I", "leukemia, stage I chronic lymphocytic", "Chronic lymphocytic leukaemia stage 1", "lymphocytic leukemia, stage I chronic", "Stage I Chronic Lymphocytic Leukemia (CLL)", "Stage I Chronic Lymphocytic Leukemia- Modified Rai Staging System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic lymphocytic leukemia stage 1", "shortest_name_length": 11}
{"curie": "UMLS:C4054374", "names": ["Nephrotic Syndrome - NEIL1 Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - NEIL1 Associated", "shortest_name_length": 37}
{"curie": "MONDO:0006788", "names": ["hydrophthalmos", "Hydrophthalmos"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hydrophthalmos", "shortest_name_length": 14}
{"curie": "MONDO:0016175", "names": ["lax skin", "Lax skin", "loose skin", "cutis laxa", "Cutis laxa", "Cutis Laxa", "Loose skin", "skin laxity", "laxa; cutis", "Skin laxity", "elastolysis", "cutis; laxa", "Elastolysis", "looses skin", "laxity; skin", "dermatolysis", "Dermatolysis", "Hanging skin", "Dermatolyses", "Chalazoderma", "skin; laxity", "dermatomegaly", "chalazodermia", "Chalazodermia", "Dermatomegaly", "Inelastic skin", "chalastodermia", "Cutis laxa, NOS", "dermatochalazia", "dermatochalasia", "Dermatochalasia", "dermatochalasis", "Hypoelastic skin", "Cutaneous laxity", "Dermatolysis, NOS", "Primary elastolysis", "Cutis laxa (disorder)", "cutis laxa (diagnosis)", "Systemic elastorrhexis", "Generalised elastolysis", "generalized elastolysis", "Generalized elastolysis", "Loose and inelastic skin", "Generalised elastorrhexis", "Generalized elastorrhexis", "Systematised elastorrhexis", "Systematized elastorrhexis", "Cutis laxa (hyperelastica)", "Generalised dermatochalasis", "Generalized dermatochalasis", "Generalized dermatochalasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutis laxa", "shortest_name_length": 8}
{"curie": "UMLS:C4726543", "names": ["Myeloid Neoplasms with Germline Predisposition and Preexisting Platelet Disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myeloid Neoplasms with Germline Predisposition and Preexisting Platelet Disorders", "shortest_name_length": 81}
{"curie": "MONDO:0018597", "names": ["bronchitis plastic", "Plastic bronchitis", "plastic bronchitis", "croupous bronchitis", "Croupous bronchitis", "croupous; bronchitis", "fibrinous bronchitis", "Fibrinous bronchitis", "bronchitis; croupous", "Membranous bronchitis", "bronchitis; membranous", "membranous; bronchitis", "Pseudo-membranous bronchitis", "pseudo-membranous bronchitis", "Plastic bronchitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "plastic bronchitis", "shortest_name_length": 18}
{"curie": "MONDO:0022646", "names": ["cardiofacial syndrome short limbs"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiofacial syndrome short limbs", "shortest_name_length": 33}
{"curie": "MONDO:0001802", "names": ["Acute tympanitis", "acute tympanitis", "acute myringitis", "Acute myringitis", "acute; myringitis", "myringitis; acute", "acute; tympanitis", "tympanitis; acute", "Acute tympanitis NOS", "Acute myringitis, NOS", "Acute tympanitis, NOS", "Acute myringitis (disorder)", "Unspecified acute myringitis", "acute myringitis (diagnosis)", "Acute myringitis, unspecified", "Acute myringitis, unspecified ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute tympanitis", "shortest_name_length": 16}
{"curie": "MONDO:0100184", "names": ["GTP cyclohydrolase I deficiency", "GTP-cyclohydrolase I deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "GTP cyclohydrolase I deficiency", "shortest_name_length": 31}
{"curie": "MONDO:0021523", "names": ["Benign Pharynx Tumor", "benign pharynx tumor", "benign pharynx neoplasm", "Benign Pharynx Neoplasm", "Benign tumor of pharynx", "Benign Tumor of Pharynx", "pharynx benign neoplasm", "benign pharyngeal tumor", "benign tumor of pharynx", "Benign Pharyngeal Tumor", "Benign tumour of pharynx", "pharyngeal neoplasm benign", "Benign neoplasm of pharynx", "Benign Pharyngeal Neoplasm", "benign neoplasm of pharynx", "benign pharyngeal neoplasm", "Pharyngeal Neoplasm Benign", "Benign pharyngeal neoplasm", "Benign Neoplasm of Pharynx", "Pharyngeal neoplasm benign", "benign tumor of the pharynx", "Benign Tumor of the Pharynx", "Benign Neoplasm of the Pharynx", "benign neoplasm of the pharynx", "Benign neoplasm of pharynx, NOS", "Benign neoplasm of the throat NOS", "Benign neoplasm of pharynx (disorder)", "benign neoplasm of pharynx (diagnosis)", "Benign neoplasm of pharynx, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of pharynx", "shortest_name_length": 20}
{"curie": "UMLS:C0276088", "names": ["e coli sepsis", "coli e sepsis", "E COLI SEPSIS", "E. Coli septicemia", "e. coli septicemia", "e coli septicaemia", "E. coli septicemia", "E. coli septicaemia", "e. coli septicaemia", "Septicemia escherichia", "Septicaemia escherichia", "sepsis; Escherichia coli", "Escherichia coli; sepsis", "Septicemia due to E. coli", "Septicemic colibacillosis", "Septicemia due to E. Coli", "Septicaemia due to E. Coli", "Escherichia coli septicemia", "Escherichia coli septicaemia", "Septicemia due to escherichia coli", "Escherichia coli septicemia (diagnosis)", "Septicemia due to Escherichia coli [E. Coli]", "Septicemia due to Escherichia coli (E. coli)", "Septicemia due to escherichia coli [E. coli]", "Septicaemia due to Escherichia coli (E. coli)", "Septicaemia due to Escherichia coli [E. Coli]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Escherichia coli septicemia", "shortest_name_length": 13}
{"curie": "UMLS:C4525891", "names": ["Pancreatic Neuroendocrine Tumor by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Neuroendocrine Tumor by AJCC v8 Stage", "shortest_name_length": 48}
{"curie": "UMLS:C0855148", "names": ["Refractory B-Lymphoblastic Lymphoma", "Refractory B Lymphoblastic Lymphoma", "Refractory Precursor B-Lymphoblastic Lymphoma", "Precursor B-Lymphoblastic Lymphoma Refractory", "Precursor B-lymphoblastic lymphoma refractory", "Precursor B-lymphoblastic lymphoma NOS refractory"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Precursor B-lymphoblastic lymphoma refractory", "shortest_name_length": 35}
{"curie": "MONDO:0011097", "names": ["RIEG2", "Rieger syndrome 2", "Rieger syndrome type 2", "Rieger syndrome, type 2", "RIEGER SYNDROME, TYPE 2", "Rieger Syndrome, Type 2", "Rieger syndrome 2 (disorder)", "Axenfeld-Rieger syndrome type 2", "Axenfeld-Rieger syndrome Type 2", "AXENFELD-RIEGER SYNDROME, TYPE 2", "Axenfeld-Rieger syndrome, type 2", "Axenfeld-Rieger Syndrome, Type 2", "Axenfeld-Rieger syndrome Type 2 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Axenfeld-Rieger syndrome type 2", "shortest_name_length": 5}
{"curie": "UMLS:C0232483", "names": ["Reflux", "reflux", "refluxs", "refluxed", "refluxing", "Reflux, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reflux", "shortest_name_length": 6}
{"curie": "MONDO:0017281", "names": ["renal caliceal diverticuli-deafness syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal caliceal diverticuli-deafness syndrome", "shortest_name_length": 44}
{"curie": "UMLS:C1336022", "names": ["Solar Radiation-Related Cancer", "Solar Radiation-Related Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Solar Radiation-Related Malignant Neoplasm", "shortest_name_length": 30}
{"curie": "DOID:9007", "names": ["SID", "SIDS", "COT death", "Cot Death", "Cot death", "cot death", "Crib death", "Cot Deaths", "Death, Cot", "crib death", "Crib Death", "crib deaths", "Death, Crib", "cot death; death", "death; cot death", "SUDDEN INFANT DEATH", "DEATH INFANT SUDDEN", "Sudden Infant Death", "INFANT DEATH SUDDEN", "Sudden infant death", "sudden infant death", "DEATH SUDDEN INFANT", "Death infant sudden", "Infant Death, Sudden", "infant; sudden death", "Death, Sudden Infant", "sudden; death, infant", "death; sudden, infant", "Sudden death in infants", "SUDDEN INFANT DEATH SYNDROME", "Sudden infant death syndrome", "sudden infant death syndrome", "Sudden Infant Death Syndrome", "infant death syndrome; sudden", "sudden; infant death syndrome", "syndrome; sudden infant death", "sudden infant death; syndrome", "Unexpected sudden death of infant", "Death, sudden, unexpected, infant", "SIDS (sudden infant death syndrome)", "sudden infant death syndrome (SIDS)", "SIDS (Sudden infant death syndrome)", "SIDS - Sudden infant death syndrome", "sudden infant death syndrome [SIDS]", "Sudden infant death syndrome (finding)", "sudden infant death syndrome (diagnosis)", "Sudden death of nonspecific cause in infancy", "death; sudden, cause unknown, infant (cot death)", "sudden; death, cause unknown, infant (cot death)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sudden infant death syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0017544", "names": ["SD1c", "SD1, Montagu type", "syndactyly type 1c", "zygodactyly type 3", "Zygodactyly, Montagu type", "syndactyly type 1, Montagu type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "zygodactyly type 3", "shortest_name_length": 4}
{"curie": "MONDO:0005095", "names": ["Spondylitis", "Spondarthritis", "spondarthritis", "arthritis spine", "Arthritis;spine", "spine arthritis", "spondylarthrosis", "spondarthropathy", "Spinal Arthritis", "spinal arthritis", "Spondylarthritis", "arthritis spinal", "spondylarthritis", "spondyloarthritis", "Arthritis, Spinal", "Spondyloarthritis", "arthritis of spine", "Spondylarthritides", "spondylarthritides", "spondylarthropathy", "Spinal Arthritides", "Arthritis of spine", "spondyloarthropathy", "Spondyloarthropathy", "osteoarthritis spine", "spine osteoarthritis", "spinal osteoarthritis", "osteoarthritis spinal", "arthritis of the spine", "osteoarthritis of spine", "Inflammatory spondylopathy", "Spondyloarthritis syndrome", "Spondyloarthritis (disorder)", "Arthritis of spine (disorder)", "seronegative spondyloarthropathy", "Seronegative Spondyloarthropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloarthropathy", "shortest_name_length": 11}
{"curie": "MONDO:0013884", "names": ["HMN5B", "HMN VB", "DSMAVB", "HMN 5B", "DHMN5B", "DHMN VB", "dHMN 5B", "distal HMN VB", "distal spinal muscular atrophy type VB", "spinal muscular atrophy, distal, type 5B", "SPINAL MUSCULAR ATROPHY, DISTAL, TYPE VB", "REEP1 neuronopathy, distal hereditary motor", "NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VB", "distal hereditary motor neuronopathy type 5B", "neuropathy, distal hereditary motor, type 5B", "neuronopathy, distal hereditary motor, type VB", "NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VB", "neuronopathy, distal hereditary motor, type 5B", "neuronopathy, distal hereditary motor caused by mutation in REEP1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuronopathy, distal hereditary motor, type 5B", "shortest_name_length": 5}
{"curie": "MONDO:0007406", "names": ["Cryofibrinogenemia, Familial Primary", "CRYOFIBRINOGENEMIA, FAMILIAL PRIMARY", "cryofibrinogenemia, familial primary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cryofibrinogenemia, familial primary", "shortest_name_length": 36}
{"curie": "MONDO:0010440", "names": ["AUTSX4", "Xp22 monosomy", "monosomy Xp22", "Xp22- syndrome", "del(Xp22) syndrome", "partial monosomy Xp22", "deletion Xp22 syndrome", "CHROMOSOME Xp22 DELETION SYNDROME", "chromosome Xp22 deletion syndrome", "susceptibility to autism, X-linked", "X-linked susceptibility to autism-4", "susceptibility to X-linked autism 4", "AUTISM, SUSCEPTIBILITY TO, X-LINKED 4", "autism, susceptibility to, X-linked 4", "autism, susceptibility to, X-linked type 4", "autism, susceptibility to, X-linked 4, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autism, susceptibility to, X-linked 4", "shortest_name_length": 6}
{"curie": "UMLS:C5668159", "names": ["Refractory Malignant Ovarian Brenner Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Malignant Ovarian Brenner Tumor", "shortest_name_length": 42}
{"curie": "MONDO:0017067", "names": ["cervicothoracic spina bifida aperta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervicothoracic spina bifida aperta", "shortest_name_length": 35}
{"curie": "UMLS:C5551425", "names": ["Dentophobia", "Dental Fear", "Dental Fears", "Odontophobia", "Dentophobias", "Fear, Dental", "Odontophobias", "Dental phobia", "Dental Phobia", "Dental Phobias", "Phobia, Dental", "Dental phobia (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dentophobia", "shortest_name_length": 11}
{"curie": "MONDO:0016980", "names": ["ATR-X-related syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ATR-X-related syndrome", "shortest_name_length": 22}
{"curie": "UMLS:C0856203", "names": ["Cervicitis infection", "Infective cervicitis", "cervicitis infection", "cervicitis infectious", "Infectious Cervicitis", "cervicitis infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infective cervicitis", "shortest_name_length": 20}
{"curie": "MONDO:0003882", "names": ["CNS fibrosarcoma", "CNS Fibrosarcoma", "Fibrosarcoma of CNS", "fibrosarcoma of CNS", "Fibrosarcoma of the CNS", "fibrosarcoma of the CNS", "Central Nervous System Fibrosarcoma", "central nervous system fibrosarcoma", "fibrosarcoma of central nervous system", "Fibrosarcoma of Central Nervous System", "fibrosarcoma of the central nervous system", "Fibrosarcoma of the Central Nervous System", "central nervous system fibrosarcoma (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system fibrosarcoma", "shortest_name_length": 16}
{"curie": "MONDO:0009983", "names": ["RETINITIS PIGMENTOSA, DEAFNESS, MENTAL RETARDATION, AND HYPOGONADISM", "retinitis pigmentosa, deafness, mental retardation, and hypogonadism", "Retinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism", "retinitis pigmentosa, deafness, intellectual disability, and hypogonadism", "retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome", "retinitis pigmentosa-intellectual disability-deafness-hypogenitalism syndrome", "retinitis pigmentosa-intellectual disability- labyrinthine deafness-hypogenitalism syndrome", "retinitis pigmentosa-intellectual disability-sensorineural hearing loss-hypogenitalism syndrome", "INSULIN-RESISTANT DIABETES WITH ACANTHOSIS NIGRICANS, HYPOGONADISM, PIGMENTARY RETINOPATHY, DEAFNESS, AND MENTAL RETARDATION", "insulin-resistant diabetes with acanthosis nigricans, hypogonadism, pigmentary retinopathy, deafness, and mental retardation", "insulin-resistant diabetes with acanthosis nigricans, hypogonadism, pigmentary retinopathy, deafness, and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa-intellectual disability-deafness-hypogenitalism syndrome", "shortest_name_length": 68}
{"curie": "UMLS:C0886487", "names": ["Recurrent Malignant Germ Cell Tumor", "recurrent childhood germ cell tumor", "recurrent childhood malignant germ cell tumor", "Recurrent Childhood Malignant Germ Cell Tumor", "Recurrent Childhood Malignant Germ Cell Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Malignant Germ Cell Tumor", "shortest_name_length": 35}
{"curie": "UMLS:C3179396", "names": ["Glanzmann Thrombasthenia, Type A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Glanzmann Thrombasthenia, Type A", "shortest_name_length": 32}
{"curie": "UMLS:C5556449", "names": ["Endometrial Mucinous Adenocarcinoma, Intestinal-Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endometrial Mucinous Adenocarcinoma, Intestinal-Type", "shortest_name_length": 52}
{"curie": "MONDO:0012034", "names": ["LGMDD2", "LGMD1F", "LGMD type 1F", "Limb-girdle muscular dystrophy type 1F", "limb-girdle muscular dystrophy type 1F", "muscular dystrophy limb-girdle type 1F", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1F", "muscular dystrophy, limb-girdle, type 1F", "Muscular Dystrophy, Limb-Girdle, Type 1F", "TNP03-related limb-girdle muscular dystrophy D2", "muscular dystrophy, limb-girdle, autosomal dominant 2", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 2", "autosomal dominant limb-girdle muscular dystrophy type 2", "Autosomal dominant limb-girdle muscular dystrophy type 1F", "Autosomal dominant limb girdle muscular dystrophy type 1F", "autosomal dominant limb-girdle muscular dystrophy type 1F", "Autosomal dominant limb girdle muscular dystrophy type 1F (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant limb-girdle muscular dystrophy type 1F", "shortest_name_length": 6}
{"curie": "UMLS:C5237825", "names": ["Advanced Esophageal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Esophageal Adenocarcinoma", "shortest_name_length": 34}
{"curie": "UMLS:C0840927", "names": ["Asomatognosia", "Neurologic neglect", "Asomatognosia (finding)", "Neurologic neglect syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Asomatognosia", "shortest_name_length": 13}
{"curie": "UMLS:C0520745", "names": ["Splenic bleeding", "Splenic hemorrhage", "spleen; hemorrhage", "hemorrhage; spleen", "Splenic haemorrhage", "Splenic hemorrhage (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Splenic hemorrhage", "shortest_name_length": 16}
{"curie": "MONDO:0100492", "names": ["Bonnevie-Ullrich", "Status Bonnevie Ullrich", "Status Bonnevie-Ullrich", "Bonnevie-Ulrich syndrome", "Bonnevie-Ullrich Syndrome", "Bonnevie Ullrich Syndrome", "Bonnevie-Ullrich syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bonnevie-Ullrich syndrome", "shortest_name_length": 16}
{"curie": "UMLS:C5238477", "names": ["Spiradenocylindroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spiradenocylindroma", "shortest_name_length": 19}
{"curie": "UMLS:C1336208", "names": ["Stage IIIA Liver Cancer", "Stage IIIA Liver Carcinoma", "Stage IIIA Liver Cell Carcinoma", "Stage IIIA Hepatocellular Cancer", "Stage IIIA Carcinoma of Liver Cells", "Stage IIIA Hepatocellular Carcinoma", "Stage IIIA Carcinoma of the Liver Cells", "Stage IIIA Hepatocellular Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Hepatocellular Carcinoma AJCC v7", "shortest_name_length": 23}
{"curie": "MONDO:0016060", "names": ["LC", "LTEC", "Tracheal Cleft", "tracheal cleft", "laryngeal cleft", "Laryngeal Cleft", "Laryngeal cleft", "Laryngotracheal cleft", "congenital cleft larynx", "Congenital cleft larynx", "Congenital Cleft Larynx", "fissure; larynx, congenital", "larynx; fissure, congenital", "Congenital laryngeal clefts", "Congenital fissure of larynx", "laryngotracheoesophageal cleft", "Laryngotracheoesophageal Cleft", "Laryngotracheoesophageal cleft", "Larnygeotracheoesophageal cleft", "Larnygeotracheoesophageal Cleft", "Posterior laryngeal cleft (PLC)", "Laryngotracheoesophageal cleft i", "laryngo-tracheo-esophageal cleft", "Laryngo-tracheo-esophageal cleft", "Anterior submucous laryngeal cleft", "Congenital cleft larynx (disorder)", "Laryngo-tracheo-esophageal diastema", "laryngo-tracheo-esophageal diastema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laryngotracheoesophageal cleft", "shortest_name_length": 2}
{"curie": "UMLS:C5667516", "names": ["Diffusion restriction", "Diffusion Restriction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffusion Restriction", "shortest_name_length": 21}
{"curie": "UMLS:C3899652", "names": ["Mixed Glioma", "childhood mixed glioma", "Childhood Mixed Glioma", "childhood gliomas, mixed", "childhood mixed glial tumors", "childhood tumors, mixed glial", "childhood glial tumors, mixed", "Brain tumor, child: Mixed glioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Mixed Glioma", "shortest_name_length": 12}
{"curie": "UMLS:C0268167", "names": ["Enteric hyperoxaluria", "Enteric Hyperoxaluria", "enteric hyperoxaluria", "Enteric hyperoxaluria (disorder)", "enteric hyperoxaluria (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Enteric hyperoxaluria", "shortest_name_length": 21}
{"curie": "MONDO:0002977", "names": ["Neurologic Autoimmune Disease", "neurologic autoimmune disease", "Nervous System Immune Diseases", "disease, neurologic autoimmune", "neurologic autoimmune diseases", "nervous system immune diseases", "Autoimmune Disease, Neurologic", "autoimmune disease, neurologic", "Neurologic Autoimmune Diseases", "Nervous System Immune Disorders", "Immune Diseases, Nervous System", "immune diseases, nervous system", "nervous system immune disorders", "diseases, neurologic autoimmune", "autoimmune diseases, neurologic", "Autoimmune Diseases, Neurologic", "immune disorders, nervous system", "Immune Disorders, Nervous System", "nervous system autoimmune disease", "nervous system autoimmune diseases", "autoimmune nervous system disorder", "Autoimmune Nervous System Disorder", "Autoimmune Nervous System Diseases", "Nervous System Autoimmune Diseases", "autoimmune nervous system diseases", "autoimmune diseases, nervous system", "Nervous system autoimmune disorders", "Autoimmune Diseases, Nervous System", "autoimmune disorders, nervous system", "autoimmune disease of nervous system", "Autoimmune Disorders, Nervous System", "autoimmune disease of the nervous system", "Autoimmune Diseases of the Nervous System", "autoimmune disorder of the nervous system", "Autoimmune Disorders of the Nervous System", "autoimmune disorders of the nervous system", "nervous system hypersensitivity reaction type II disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune disorder of the nervous system", "shortest_name_length": 29}
{"curie": "MONDO:0015262", "names": ["brachyolmia", "Brachyolmia", "brachyrachia", "Brachyolmia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachyolmia", "shortest_name_length": 11}
{"curie": "MONDO:0015884", "names": ["AD-HED", "autosomal dominant anhidrotic ectodermal dysplasia", "autosomal dominant hypohidrotic ectodermal dysplasia", "hypohidrotic ectodermal dysplasia, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant hypohidrotic ectodermal dysplasia", "shortest_name_length": 6}
{"curie": "UMLS:C4684885", "names": ["Recurrent Primary Cutaneous Lymphoma", "Recurrent Primary Cutaneous (Skin) Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Primary Cutaneous Lymphoma", "shortest_name_length": 36}
{"curie": "UMLS:C5394780", "names": ["Anaplastic lymphoma kinase-positive non-small cell lung cancer", "Anaplastic lymphoma kinase fusion oncogene positive non-small cell lung cancer", "anaplastic lymphoma kinase fusion oncogene positive non-small cell neoplasm of lung", "ALK (anaplastic lymphoma kinase) fusion oncogene positive non-small cell lung cancer", "Anaplastic lymphoma kinase fusion oncogene positive non-small cell lung cancer (disorder)", "anaplastic lymphoma kinase fusion oncogene positive non-small cell neoplasm of lung (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anaplastic lymphoma kinase fusion oncogene positive non-small cell lung cancer", "shortest_name_length": 62}
{"curie": "MONDO:0018654", "names": ["dropped head syndrome", "isolated neck extensor myopathy", "idiopathic dropped head syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic dropped head syndrome", "shortest_name_length": 21}
{"curie": "MONDO:0011371", "names": ["Familial hydroa vacciniforme", "familial hydroa vacciniforme", "hydroa vacciniforme, familial", "HYDROA VACCINIFORME, FAMILIAL", "Hydroa vacciniforme, familial", "hereditary hydroa vacciniforme"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hydroa vacciniforme, familial", "shortest_name_length": 28}
{"curie": "UMLS:C5239285", "names": ["Locally Advanced Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Adenocarcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0018071", "names": ["Edwards", "E3 trisomy", "18 trisomy", "Trisomy 18", "E3 Trisomy", "trisomy 18", "trisomy; 18", "edward syndrome", "trisomy type 18", "Edwards Syndrome", "EDWARDS SYNDROME", "edwards syndrome", "Edwards syndrome", "Edwards' syndrome", "Edward's syndrome", "edward's syndrome", "trisomy 18 syndrome", "Trisomy 18 syndrome", "Trisomy 18 Syndrome", "trisomy E (formerly)", "Trisomy 18 Syndromes", "trisomy; syndrome, 18", "chromosome 18 trisomy", "[OBSOLETE] Trisomy 18", "syndrome; trisomy, 18", "chromosome; 18, trisomy", "trisomy 16-18 (formerly)", "chromosome 18 duplication", "Chromosome 18 duplication", "Complete Trisomy 18 Syndrome", "complete trisomy 18 syndrome", "Complete trisomy 18 syndrome", "Edwards' syndrome, unspecified", "Complete trisomy 18 syndrome (disorder)", "Chromosomal imbalance syndrome, pair 18, trisomy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trisomy 18", "shortest_name_length": 7}
{"curie": "MONDO:0600027", "names": ["congenital right-sided heart lesions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital right-sided heart lesions", "shortest_name_length": 36}
{"curie": "UMLS:C3853541", "names": ["Erosive duodenitis", "erosive duodenitis", "Erosive Duodenitis", "Duodenitis, Erosive", "erosive duodenopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Erosive Duodenitis", "shortest_name_length": 18}
{"curie": "MONDO:0022824", "names": ["congenital craniosynostosis maternal hyperthyroiditis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital craniosynostosis maternal hyperthyroiditis", "shortest_name_length": 53}
{"curie": "UMLS:C2348985", "names": ["Hodgkin Lymphoma by Clinical Course"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin Lymphoma by Clinical Course", "shortest_name_length": 35}
{"curie": "MONDO:0011462", "names": ["FRA", "fra", "papa", "PAPA", "PAPAS", "Papas", "PAPA syndrome", "PAPA SYNDROME", "papa syndrome", "Familial recurrent arthritis", "familial recurrent arthritis", "FAMILIAL RECURRENT ARTHRITIS", "Pyogenic Arthritis, Pyoderma Gangrenosum and Acne", "pyogenic arthritis, pyoderma gangrenosum and acne", "Pyogenic arthritis, pyoderma gangrenosum, and acne", "pyogenic arthritis-pyoderma gangrenosum-acne syndrome", "Pyogenic arthritis-pyoderma gangrenosum-acne syndrome", "Pyogenic arthritis, pyoderma gangrenosum, acne syndrome", "pyogenic arthritis, pyoderma gangrenosum, acne syndrome", "pyogenic STERILE arthritis, pyoderma gangrenosum, and acne", "PYOGENIC STERILE ARTHRITIS, PYODERMA GANGRENOSUM, AND ACNE", "Pyogenic Sterile Arthritis, Pyoderma Gangrenosum, and Acne", "PAPA (pyogenic arthritis, pyoderma gangrenosum, acne) syndrome", "Pyogenic arthritis, pyoderma gangrenosum, and severe cystic acne", "pyogenic arthritis, pyoderma gangrenosum, and severe cystic acne", "Pyogenic sterile arthritis pyoderma gangrenosum and acne syndrome", "Pyogenic arthritis, pyoderma gangrenosum, and acne syndrome [PAPA]", "Pyogenic arthritis, pyoderma gangrenosum, acne syndrome (disorder)", "pyogenic arthritis, pyoderma gangrenosum, acne syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyogenic arthritis-pyoderma gangrenosum-acne syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0021482", "names": ["benign middle Ear tumor", "Benign Middle Ear Tumor", "benign auditory neoplasm", "auditory neoplasm benign", "middle ear benign neoplasm", "Benign tumor of middle ear", "Benign Tumor of Middle Ear", "Benign Middle Ear Neoplasm", "Benign middle ear neoplasm", "benign middle Ear neoplasm", "benign tumor of middle Ear", "Benign tumour of middle ear", "Benign Neoplasm of Middle Ear", "Benign neoplasm of middle ear", "benign neoplasm of middle ear", "Benign Tumor of the Middle Ear", "benign tumor of the middle Ear", "benign neoplasm of the middle Ear", "Benign Neoplasm of the Middle Ear", "benign auditory neoplasm (diagnosis)", "auditory neoplasm benign of middle ear", "Benign neoplasm of middle ear (disorder)", "benign neoplasm of middle ear (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of middle ear", "shortest_name_length": 23}
{"curie": "MONDO:0001170", "names": ["Hemiplegia", "HEMIPLEGIA", "hemiplegia", "Hemiplegias", "hemiparalysis", "Hemiplegia, NOS", "hemiplegia was seen", "Infantile hemiplegia", "hemiplegia (symptom)", "Infantile Hemiplegia", "infantile hemiplegia", "hemiplegia infantile", "infantile; hemiplegia", "Hemiplegia (disorder)", "Infantile Hemiplegias", "Hemiplegia, Infantile", "hemiplegia; infantile", "Hemiplegias, Infantile", "hemiplegia (diagnosis)", "Hemiplegia, unspecified", "Infantile hemiplegia NOS", "PARALYSIS ONE SIDE OF BODY", "Paralysis one side of body", "paralysis of one side of body", "Infantile cerebral hemiplegia", "Paralysis on one side of body", "hemiplegia (physical finding)", "postnatal infantile hemiplegia", "Postnatal infantile hemiplegia", "Infantile hemiplegia (disorder)", "Postnatal infantile hemiplegia NOS", "Hemiplegia (paralysis on one side)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemiplegia", "shortest_name_length": 10}
{"curie": "MONDO:0001323", "names": ["infant gynecomastia", "Infant Gynecomastia", "Gynecomastia, Infant", "Newborn Gynecomastia", "Gynecomastia, Newborn", "neonatal gynecomastia", "Neonatal gynecomastia", "Neonatal gynaecomastia", "neonatal gynaecomastia", "congestion; breast, newborn", "NEONATAL BREAST ENGORGEMENT", "Neonatal Breast Enlargement", "breast; engorgement, newborn", "Breast Engorgement in Newborn", "Breast engorgement in newborn", "Breast engorgement of newborn", "breast engorgement in newborn", "Breast engorgement of new born", "neonatal gynecomastia (diagnosis)", "Breast engorgement in newborn (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infant gynecomastia", "shortest_name_length": 19}
{"curie": "MONDO:0003377", "names": ["Bile Duct Leiomyosarcoma", "bile duct leiomyosarcoma", "leiomyosarcoma of bile duct", "Leiomyosarcoma of Bile Duct", "Leiomyosarcoma of the Bile Duct", "leiomyosarcoma of the bile duct", "extrahepatic bile duct leiomyosarcoma", "Extrahepatic Bile Duct Leiomyosarcoma", "Leiomyosarcoma of Extrahepatic Bile Duct", "leiomyosarcoma of extrahepatic bile duct", "Leiomyosarcoma of the Extrahepatic Bile Duct", "leiomyosarcoma of the extrahepatic bile duct", "leiomyosarcoma of extrahepatic bile duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extrahepatic bile duct leiomyosarcoma", "shortest_name_length": 24}
{"curie": "MONDO:0014190", "names": ["COXPD17", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 17", "combined oxidative phosphorylation deficiency 17", "Combined oxidative phosphorylation defect type 17", "combined oxidative phosphorylation defect type 17", "ELAC2 combined oxidative phosphorylation deficiency", "combined oxidative phosphorylation deficiency type 17", "COXPD17 - combined oxidative phosphorylation defect type 17", "Combined oxidative phosphorylation defect type 17 (disorder)", "combined oxidative phosphorylation deficiency caused by mutation in ELAC2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation defect type 17", "shortest_name_length": 7}
{"curie": "MONDO:0002356", "names": ["PANCREAS DISEASE", "pancreas disease", "disease pancreas", "diseases pancrea", "Disease;pancreas", "DISORDER PANCREAS", "pancreas diseases", "Pancreas disorder", "Disorder pancreas", "pancreas disorder", "diseases pancreas", "PANCREAS DISORDER", "disorders pancreas", "Pancreatic disease", "Pancreas--Diseases", "Pancreatic Disease", "disease pancreatic", "pancreatic disease", "Disease, Pancreatic", "disease, pancreatic", "of pancreas disease", "PANCREATIC DISORDER", "Pancreatic disorder", "pancreatic disorder", "disease of pancreas", "pancreatic diseases", "Disease of pancreas", "Pancreatic Diseases", "diseases pancreatic", "Pancreatic Disorder", "pancreatic disorders", "disorders pancreatic", "Disorder of pancreas", "diseases, pancreatic", "diseases of pancreas", "Diseases, Pancreatic", "disorder of pancreas", "Diseases of pancreas", "disease of the pancreas", "Pancreatic disorder NOS", "diseases of the pancreas", "Disease of pancreas, NOS", "DISEASES OF THE PANCREAS", "Disorder of pancreas, NOS", "Abnormality of the pancreas", "pancreas disease or disorder", "Disorder of pancreas (disorder)", "disease (or disorder); pancreas", "Unspecified disease of pancreas", "disease or disorder of pancreas", "pancreatic disorders (diagnosis)", "Disease of pancreas, unspecified", "Diseases and Syndromes of Pancreas", "Other specified diseases of pancreas", "pancreatic disorders other specified diseases", "Other specified diseases of pancreas (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreas disorder", "shortest_name_length": 16}
{"curie": "UMLS:C4761609", "names": ["Locally Advanced Squamous Non-Small Cell Lung Carcinoma", "Locally Advanced Lung Non-Small Cell Squamous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Lung Non-Small Cell Squamous Carcinoma", "shortest_name_length": 55}
{"curie": "MONDO:0007094", "names": ["AI1A", "Microdontia, Generalized", "LAMB3 amelogenesis imperfecta", "Amelogenesis imperfecta type 1", "amelogenesis imperfecta type 1A", "amelogenesis imperfecta type IA", "amelogenesis imperfecta, type 1A", "AMELOGENESIS IMPERFECTA, TYPE IA", "amelogenesis imperfecta, type IA", "Hypoplastic amelogenesis imperfecta", "Amelogenesis imperfecta, hypoplastic", "Amelogenesis imperfecta - hypoplastic", "Hypoplastic type amelogenesis imperfecta", "Amelogenesis imperfecta, hypoplastic type", "local hypoplastic amelogenesis imperfecta", "amelogenesis imperfecta local hypoplastic", "Amelogenesis Imperfecta, Hypoplastic Type", "amelogenesis imperfecta hypoplastic type IA", "amelogenesis imperfecta, hypoplastic type 1A", "AMELOGENESIS IMPERFECTA, HYPOPLASTIC TYPE IA", "Amelogenesis imperfecta local hypoplastic form", "Local, hypoplastic type of amelogenesis imperfecta", "amelogenesis imperfecta caused by mutation in LAMB3", "Amelogenesis imperfecta, hypoplastic type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amelogenesis imperfecta type 1A", "shortest_name_length": 4}
{"curie": "UMLS:C4727189", "names": ["Refractory Colon Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Colon Carcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0004804", "names": ["Dacryadenitis", "Dacryoadenitis", "dacryoadenitis", "Dacryoadenitides", "Dacryoadenitis, NOS", "infection; lacrimal gland", "lacrimal gland; infection", "Dacryoadenitis (disorder)", "dacryoadenitis (diagnosis)", "Unspecified dacryoadenitis", "LACRIMAL GLAND INFLAMMATION", "lacrimal gland inflammation", "Dacryoadenitis, unspecified", "gland inflammation lacrimal", "inflammation; lacrimal gland", "lacrimal gland; inflammation", "inflammation of lacrimal gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dacryoadenitis", "shortest_name_length": 13}
{"curie": "MONDO:0016066", "names": ["cleft sternum", "Cleft sternum", "Bifid sternum", "Sternal cleft", "Sternoschisis", "sternum cleft", "sternal cleft", "Sternum bifidum", "sternum bifidum", "bifidum; sternum", "sternum; bifidum", "Bipartite sternum", "Congenital sternal cleft", "congenital sternal cleft", "Sternum bifidum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sternal cleft", "shortest_name_length": 13}
{"curie": "MONDO:0008440", "names": ["Fitzsimmons-Walson-Mellor syndrome", "Fitzsimmons Walson Mellor syndrome", "spastic paraplegia - nephritis - deafness", "Spastic paraplegia-nephritis-deafness syndrome", "spastic paraplegia-nephritis-deafness syndrome", "Spastic paraplegia, nephritis, deafness syndrome", "Spastic paraplegia-nephritis-hearing loss syndrome", "Spastic paraplegia, nephritis, deafness syndrome (disorder)", "spastic paraplegia, sensorineural deafness, mental retardation, and progressive nephropathy", "Spastic Paraplegia, Sensorineural Deafness, Mental Retardation, And Progressive Nephropathy", "SPASTIC PARAPLEGIA, SENSORINEURAL DEAFNESS, MENTAL RETARDATION, AND PROGRESSIVE NEPHROPATHY", "spastic paraplegia, sensorineural deafness, intellectual disability, and progressive nephropathy", "spastic paraplegia, bilateral sensorineural deafness, intellectual retardation, and progressive nephropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic paraplegia-nephritis-deafness syndrome", "shortest_name_length": 34}
{"curie": "MONDO:0006574", "names": ["Lipomas", "LIPOMATOSES", "Lipomatoses", "Lipomatosis", "lipomatoses", "lipomatosis", "lipoma multiple", "Lipomatosis NOS", "LIPOMA MULTIPLE", "multiple lipoma", "Madelung Disease", "lipomas multiple", "Multiple lipomas", "Madelung disease", "Lipomatosis, NOS", "Multiple lipomata", "multiple lipomata", "Madelung's Disease", "Madelung's disease", "Multiple fatty lumps", "Lipomatosis (disorder)", "lipomatosis (diagnosis)", "Launois-Bensaude syndrome", "Launois-Bensaude Syndrome", "Multiple lipomata (disorder)", "multiple lipomata (diagnosis)", "Lipomatosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lipomatosis", "shortest_name_length": 7}
{"curie": "MONDO:0005970", "names": ["Staphylococcal Pneumonia", "PNEUMONIA STAPHYLOCOCCAL", "Staphylococcus pneumonia", "Pneumonia staphylococcal", "Staphylococcal pneumonia", "staphylococcal pneumonia", "pneumonia staphylococcal", "STAPHYLOCOCCAL PNEUMONIA", "Staphylococcal Pneumonias", "Pneumonia, Staphylococcal", "staphylococcus; pneumonia", "PNEUMONIA, STAPHYLOCOCCAL", "pneumonia; staphylococcus", "Pneumonias, Staphylococcal", "Pneumonia due to staphylococcus", "Pneumonia due to Staphylococcus", "Staphylococcus caused pneumonia", "Staphylococcal pneumonia (disorder)", "staphylococcal pneumonia (diagnosis)", "Pneumonia due to Staphylococcus, unspecified", "Pneumonia due to staphylococcus, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "staphylococcal pneumonia", "shortest_name_length": 24}
{"curie": "MONDO:0007115", "names": ["Autosomal dominant angioma serpiginosum", "autosomal dominant angioma serpiginosum", "angioma serpiginosum, autosomal dominant", "Angioma serpiginosum, autosomal dominant", "ANGIOMA SERPIGINOSUM, AUTOSOMAL DOMINANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angioma serpiginosum, autosomal dominant", "shortest_name_length": 39}
{"curie": "UMLS:C1266025", "names": ["TSA", "Serrated Adenoma", "Serrated adenoma", "serrated adenoma", "adenomas serrated", "Serrated Adenoma Type II", "Traditional serrated adenoma", "Traditional Serrated Adenoma", "Mixed adenomatous and hyperplastic polyp", "Serrated adenoma (morphologic abnormality)", "Traditional serrated adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Traditional Serrated Adenoma", "shortest_name_length": 3}
{"curie": "MONDO:0017775", "names": ["Stanton", "Whitmore", "Melioidosis", "melioidosis", "MELIOIDOSIS", "Melioidoses", "PSEUDOCHOLERA", "Pseudoglanders", "pseudoglanders", "STANTON DISEASE", "WHITMORE DISEASE", "Whitmore Disease", "Whitmore disease", "stanton's disease", "Stanton's disease", "Whitmore's disease", "Melioidosis (disorder)", "melioidosis (diagnosis)", "B pseudomallei infection", "Melioidosis, unspecified", "Pseudomonas; pseudomallei", "pseudomallei; Pseudomonas", "melioidosis acute fulminating", "Nightcliff gardener's disease", "infection by Whitmore bacillus", "subacute and chronic melioidosis", "Subacute and chronic melioidosis", "Acute and fulminating melioidosis", "acute and fulminating melioidosis", "Pseudomonas pseudomallei infection", "Burkholderia pseudomallei Infection", "infection; Malleomyces pseudomallei", "Malleomyces pseudomallei; infection", "Burkholderia pseudomallei infection", "infection; Pseudomonas, pseudomallei", "Infection due to Whitmore's bacillus", "Pseudomonas; infection, pseudomallei", "Burkholderia pseudomallei Infections", "Infection, Burkholderia pseudomallei", "Infections, Burkholderia pseudomallei", "infection by Malleomyces pseudomallei", "infection by Pseudomonas pseudomallei", "infection by Burkholderia pseudomallei", "Infection due to Malleomyces pseudomallei", "melioidosis acute fulminating (diagnosis)", "Infection due to malleomyces pseudomallei", "Infection due to Pseudomonas pseudomallei", "infection by Whitmore bacillus (diagnosis)", "Infection due to Burkholderia pseudomallei", "Subacute and chronic melioidosis (disorder)", "Acute and fulminating melioidosis (disorder)", "Burkholderia pseudomallei infectious disease", "Infection due to Pseudomonas pseudomallei NOS", "Burkholderia pseudomallei disease or disorder", "melioidosis due to infection by Whitmore bacillus", "infection by Pseudomonas pseudomallei (diagnosis)", "infection by Malleomyces pseudomallei (diagnosis)", "infection by Burkholderia pseudomallei (diagnosis)", "Burkholderia pseudomallei caused disease or disorder", "melioidosis due to infection by pseudomonal pseudomallei", "melioidosis due to infection by malleomyces pseudomallei", "melioidosis due to infection by Burkholderia pseudomallei"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melioidosis", "shortest_name_length": 7}
{"curie": "UMLS:C0521622", "names": ["bilateral hydronephrosis", "Bilateral hydronephrosis", "hydronephrosis bilateral", "Hydronephrosis, bilateral", "hydronephrosis bilaterally", "hydronephrosis on both sides", "Bilateral hydronephrosis (disorder)", "hydronephrosis on both sides (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bilateral hydronephrosis", "shortest_name_length": 24}
{"curie": "UMLS:C4288232", "names": ["Sex Chromosome Differences of Sex Development"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sex Chromosome Differences of Sex Development", "shortest_name_length": 45}
{"curie": "MONDO:0010546", "names": ["central incisors, absence of", "CENTRAL INCISORS, ABSENCE OF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central incisors, absence of", "shortest_name_length": 28}
{"curie": "UMLS:C4524457", "names": ["Mucosal Melanoma of the Head and Neck by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mucosal Melanoma of the Head and Neck by AJCC v7 Stage", "shortest_name_length": 54}
{"curie": "UMLS:C4054729", "names": ["Infant ALL with MLL Rearrangement", "Infant Acute Lymphoblastic Leukemia with MLL Rearrangement", "Infant Acute Lymphoblastic Leukemia with MLL Gene Rearrangement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infant Acute Lymphoblastic Leukemia with MLL Rearrangement", "shortest_name_length": 33}
{"curie": "MONDO:0004425", "names": ["hyperthyroid", "HYPERTHYROID", "Hyperthyroid", "Hyperthyroids", "HYPERTHYROIDISM", "Hyperthyroidism", "hyperthyroidism", "Overactive thyroid", "overactive thyroid", "Overactive Thyroid", "Hyperthyroidism NOS", "hyperthyroidism nos", "Hyperthyroidism, NOS", "Primary hyperthyroidism", "Primary Hyperthyroidism", "Hyperthyroidism, Primary", "Hyperthyroidism (disorder)", "hyperthyroidism (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperthyroidism", "shortest_name_length": 12}
{"curie": "MONDO:0004732", "names": ["stage 0 kidney carcinoma", "kidney carcinoma in situ", "kidney in situ carcinoma", "Carcinoma in situ of kidney", "carcinoma in situ of kidney", "Carcinoma in situ of kidney, NOS", "Carcinoma in situ of kidney (disorder)", "carcinoma in situ of kidney (diagnosis)", "Carcinoma in situ of other and unspecified urinary organs"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kidney carcinoma in situ", "shortest_name_length": 24}
{"curie": "MONDO:0018677", "names": ["Heterotaxy", "heterotaxy", "Heterotaxis", "heterotaxia", "Heterotaxia", "Situs ambiguus", "situs ambiguus", "Situs Ambiguus", "Ambiguus, Situs", "Situs ambiguous", "situs ambiguous", "situs abnormality", "Isomerism sequence", "visceral inversion", "Laterality sequence", "Heterotaxy syndrome", "Visceral heterotaxy", "Visceral Heterotaxy", "laterality sequence", "Heterotaxy Syndrome", "heterotaxy syndrome", "visceral heterotaxy", "Heterotaxy, Visceral", "Heterotaxia Syndrome", "Heterotaxy Syndromes", "inversion of viscera", "Syndrome, Heterotaxy", "heterotaxia syndrome", "heterotaxy, visceral", "Syndromes, Heterotaxy", "Lateralization defect", "Visceral Heterotaxies", "lateralization defect", "visceral transposition", "Heterotaxies, Visceral", "partial situs inversus", "Visceral transposition", "Partial situs inversus", "Situs Ambiguus Viscerum", "situs inversus viscerum", "Ambiguus Viscerum, Situs", "Viscerum, Situs Ambiguus", "transposition of viscera", "Situs Ambiguus Viscerums", "Laterality sequence, NOS", "incomplete situs inversus", "Situs ambiguus (disorder)", "Viscerums, Situs Ambiguus", "Incomplete situs inversus", "Ambiguus Viscerums, Situs", "Laterality sequence (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "visceral heterotaxy", "shortest_name_length": 10}
{"curie": "UMLS:C0013926", "names": ["air embolus", "Air embolus", "embolus air", "gas embolism", "Embolus, air", "Gas embolism", "AIR EMBOLISM", "Air embolism", "Air Embolism", "Gas Embolism", "aeroembolism", "embolism air", "Aeroembolism", "air embolism", "AEROEMBOLISM", "Embolism, Gas", "Air Embolisms", "Gas Embolisms", "embolism; air", "gas embolisms", "Embolism, Air", "air embolisms", "Embolisms, Gas", "Embolisms, Air", "Air embolism (disorder)", "air embolism (diagnosis)", "Air embolus (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Air Embolism", "shortest_name_length": 11}
{"curie": "UMLS:C5206599", "names": ["Paratesticular Rhabdomyoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paratesticular Rhabdomyoma", "shortest_name_length": 26}
{"curie": "MONDO:0015352", "names": ["HMN2", "dSMA2", "dHMN2", "HMN II", "distal spinal muscular atrophy type 2", "distal hereditary motor neuropathy type 2", "distal hereditary motor neuropathy type II", "distal hereditary motor neuronopathy type 2", "Distal Hereditary Motor Neuropathy, Type II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal hereditary motor neuropathy type 2", "shortest_name_length": 4}
{"curie": "MONDO:0056805", "names": ["nerve benign granular cell tumor", "benign granular cell tumor of nerve", "Benign Peripheral Nerve Granular Cell Tumor", "benign peripheral nerve granular cell tumor", "Benign Peripheral Nerve Granular Cell Neoplasm", "benign peripheral nerve granular cell neoplasm", "Benign Granular Cell Tumor of Peripheral Nerve", "benign granular cell tumor of peripheral nerve", "benign granular cell neoplasm of peripheral nerve", "Benign Granular Cell Neoplasm of Peripheral Nerve", "Benign Granular Cell Tumor of the Peripheral Nerve", "benign granular cell tumor of the peripheral nerve", "benign granular cell neoplasm of the peripheral nerve", "Benign Granular Cell Neoplasm of the Peripheral Nerve"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign peripheral nerve granular cell tumor", "shortest_name_length": 32}
{"curie": "UMLS:C5205653", "names": ["Recurrent Anaplastic Ganglioglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Anaplastic Ganglioglioma", "shortest_name_length": 34}
{"curie": "UMLS:C3899979", "names": ["BCLC Stage B Hepatocellular Cancer", "BCLC Stage B Hepatocellular Carcinoma", "Barcelona Clinic Liver Cancer Stage B Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "BCLC Stage B Hepatocellular Carcinoma", "shortest_name_length": 34}
{"curie": "UMLS:C0948447", "names": ["chromosomal mutation", "Chromosomal mutation", "chromosomal mutations", "Chromosomal mutation NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chromosomal mutation", "shortest_name_length": 20}
{"curie": "MONDO:0033651", "names": ["MC4DN16", "mitochondrial complex 4 deficiency, nuclear type 16", "MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 16", "mitochondrial complex IV deficiency, nuclear type 16"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 4 deficiency, nuclear type 16", "shortest_name_length": 7}
{"curie": "MONDO:0030463", "names": ["SPGF58", "SPERMATOGENIC FAILURE 58", "spermatogenic failure 58"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 58", "shortest_name_length": 6}
{"curie": "UMLS:C1137478", "names": ["Degenerative Retinoschisis", "Degenerative Retinoschises", "Retinoschises, Degenerative", "Retinoschisis, Degenerative"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retinoschisis, Degenerative", "shortest_name_length": 26}
{"curie": "MONDO:0700152", "names": ["canine hepatocellular carcinoma", "Canine Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canine hepatocellular carcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C4522160", "names": ["Invasive mucinous adenocarcinoma", "Invasive Lung Mucinous Adenocarcinoma", "Mucinous Invasive Lung Adenocarcinoma", "Mucinous Bronchioloalveolar Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Invasive Lung Mucinous Adenocarcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C5420812", "names": ["Iris Epithelioid Cell Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Iris Epithelioid Cell Melanoma", "shortest_name_length": 30}
{"curie": "MONDO:0009266", "names": ["GD2", "Gd 2", "GD II", "Gaucher disease type 2", "Type 2 Gaucher Disease", "Gaucher Disease Type 2", "Gaucher disease, type 2", "Gaucher disease type II", "Gaucher Disease, Type 2", "Gaucher disease, type II", "GAUCHER DISEASE, TYPE II", "Gaucher Disease, Type II", "Infantile Gaucher Disease", "Infantile Gaucher disease", "Gaucher's disease type II", "Disease, Infantile Gaucher", "Gaucher's disease, type II", "Gaucher Disease, Infantile", "Infantile Gaucher's disease", "Cerebral acute Gaucher disease", "Acute cerebral Gaucher's disease", "Infantile Cerebral Gaucher Disease", "Gaucher Disease, Type 2 (disorder)", "infantile cerebral Gaucher disease", "Infantile cerebral Gaucher disease", "Acute Neuronopathic Gaucher Disease", "acute neuronopathic Gaucher disease", "Acute neuronopathic Gaucher disease", "Gaucher Disease, Infantile Cerebral", "Gaucher disease, infantile cerebral", "Gaucher disease type II (diagnosis)", "Infantile cerebral Gaucher's disease", "Gaucher Disease, Acute Neuronopathic", "Glucocerebrosidase deficiency type II", "Acute neuronopathic Gaucher's disease", "GAUCHER DISEASE, ACUTE NEURONOPATHIC TYPE", "Gaucher Disease, Acute Neuronopathic Type", "Glucosylceramidase deficiency, acute type", "Gaucher disease, acute neuronopathic type", "Gaucher's disease II, infantile form, (cerebral)", "Acute neuronopathic Gaucher's disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gaucher disease type II", "shortest_name_length": 3}
{"curie": "MONDO:0000486", "names": ["Facial dystonia", "Facial Dystonia", "Craniofacial dystonia", "craniofacial dystonia", "cranio-facial dystonia", "Abnormal facial muscle tone", "Abnormal craniofacial posture", "Distorted craniofacial posture", "Abnormal craniofacial muscle tone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniofacial dystonia", "shortest_name_length": 15}
{"curie": "MONDO:0015559", "names": ["lymphoadenopathic mastocytosis with eosinophilia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphoadenopathic mastocytosis with eosinophilia", "shortest_name_length": 48}
{"curie": "UMLS:C0334000", "names": ["Glandular Hyperplasia", "Glandular hyperplasia", "glandular hyperplasia", "Hyperplasia, glandular", "adenomatoid hyperplasia", "adenomatous hyperplasia", "Adenomatoid hyperplasia", "HYPERPLASIA ADENOMATOUS", "Adenomatous hyperplasia", "Hyperplasia, adenomatoid", "Glandular hyperplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenomatous hyperplasia", "shortest_name_length": 21}
{"curie": "UMLS:C2981674", "names": ["stage IA pancreatic cancer", "Stage IA Pancreatic Cancer", "pancreatic cancer, stage IA", "Stage IA Pancreatic Cancer AJCC v6 and v7", "Stage IA Exocrine and Endocrine Pancreatic Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Pancreatic Cancer AJCC v6 and v7", "shortest_name_length": 26}
{"curie": "MONDO:0020353", "names": ["von Hippel anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "von Hippel anomaly", "shortest_name_length": 18}
{"curie": "MONDO:0032790", "names": ["NEDCFSA", "neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities", "NEURODEVELOPMENTAL DISORDER WITH COARSE FACIES AND MILD DISTAL SKELETAL ABNORMALITIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities", "shortest_name_length": 7}
{"curie": "MONDO:0032923", "names": ["SCAR28", "autosomal recessive spinocerebellar ataxia 28", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 28", "spinocerebellar ataxia, autosomal recessive 28"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia, autosomal recessive 28", "shortest_name_length": 6}
{"curie": "UMLS:C5418297", "names": ["Locally Advanced Clear Cell Renal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Clear Cell Renal Cell Carcinoma", "shortest_name_length": 48}
{"curie": "MONDO:0013030", "names": ["CMD1BB", "dilated cardiomyopathy 1BB", "cardiomyopathy, dilated, 1BB", "Cardiomyopathy, Dilated, 1BB", "CARDIOMYOPATHY, DILATED, 1BB", "dilated cardiomyopathy type 1BB", "cardiomyopathy, dilated, type 1Bb", "DSG2 familial isolated dilated cardiomyopathy", "familial isolated dilated cardiomyopathy caused by mutation in DSG2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1BB", "shortest_name_length": 6}
{"curie": "UMLS:C3810813", "names": ["Anticonvulsant Hypersensitivity Syndrome", "Anti-Convulsant Hypersensitivity Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anticonvulsant Hypersensitivity Syndrome", "shortest_name_length": 40}
{"curie": "MONDO:0700041", "names": ["NBLST2", "susceptibility to neuroblastoma 2", "NEUROBLASTOMA, SUSCEPTIBILITY TO, 2", "neuroblastoma, susceptibility to, 2", "neuroblastoma, susceptibility to, type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuroblastoma, susceptibility to, 2", "shortest_name_length": 6}
{"curie": "MONDO:0029135", "names": ["MDDGC2", "MDDGC8", "LGMDR24", "LGMD-POMGNT2 related myopathy", "muscular dystrophy-dystroglycanopathy type C8", "autosomal recessive limb-girdle muscular dystrophy 24", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 24", "muscular dystrophy, limb-girdle, autosomal recessive 24", "muscular dystrophy-dystroglycanopathy (limb-girdle) type C, 8", "muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 8", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 8", "muscular dystrophy-dystroglycanopathy (limb-girdle), TYPE C, 8", "muscular dystrophy-dystroglycanopathy, limb-girdle, POMGNT2-related", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, POMGNT2-RELATED", "Muscular dystrophy-dystroglycanopathy, limb-girdle, POMGNT2-related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 8", "shortest_name_length": 6}
{"curie": "UMLS:C0919874", "names": ["Post procedural bleeding", "Post procedural hemorrhage", "Post Procedural Hemorrhage", "Post procedural haemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post procedural hemorrhage", "shortest_name_length": 24}
{"curie": "MONDO:0007350", "names": ["coloboma, ocular", "Uveoretinal Coloboma", "COLOBOMA, UVEORETINAL", "Coloboma, Uveoretinal", "Coloboma, uveoretinal", "coloboma, Uveoretinal", "Uveoretinal Colobomas", "Colobomas, Uveoretinal", "coloboma, ocular, autosomal dominant", "coloboma of iris, choroid, and retina"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coloboma, ocular, autosomal dominant", "shortest_name_length": 16}
{"curie": "MONDO:0016968", "names": ["trisomy 18q", "18q trisomy", "Trisomy 18q", "18q syndrome", "18q+ syndrome", "18q duplication", "Duplication 18q", "dup(18q) syndrome", "18q partial trisomy", "partial trisomy 18q", "chromosome 18q trisomy", "duplication 18q syndrome", "18q duplication syndrome", "Chromosome 18, trisomy 18q", "chromosome 18q duplication", "partial trisomy of chromosome 18q", "chromosome 18q duplication syndrome", "partial duplication of chromosome 18q", "partial trisomy of the long arm of chromosome 18", "partial duplication of the long arm of chromosome 18", "partial trisomy of the long arm of chromosome type 18"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial trisomy of the long arm of chromosome 18", "shortest_name_length": 11}
{"curie": "UMLS:C0019081", "names": ["Anorectal hemorrhage", "Anorectal haemorrhage", "rectal and anal hemorrhage", "Hemorrhage of Rectum and Anus", "Hemorrhage of anus and rectum", "Hemorrhage of rectum and anus", "Haemorrhage of rectum and anus", "Haemorrhage of anus and rectum", "rectal and anal hemorrhage (diagnosis)", "Hemorrhage of rectum and anus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemorrhage of rectum and anus", "shortest_name_length": 20}
{"curie": "UMLS:C0016325", "names": ["FLUOROSIS", "Fluorosis", "fluorosis", "Fluoride Poisoning", "Poisoning, Fluoride", "Fluoride Poisonings", "Poisonings, Fluoride", "Fluorosis (disorder)", "Fluoride intoxication", "FLUORIDE INTOXICATION", "Chronic fluoride poisoning"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fluoride Poisoning", "shortest_name_length": 9}
{"curie": "MONDO:0006964", "names": ["HYPERPARATHYROIDISM SECONDARY", "secondary hyperparathyroidism", "Secondary Hyperparathyroidism", "Secondary hyperparathyroidism", "hyperparathyroidism secondary", "Hyperparathyroidism secondary", "Secondary Hyperparathyroidisms", "Hyperparathyroidism, secondary", "secondary; hyperparathyroidism", "HYPERPARATHYROIDISM, SECONDARY", "hyperparathyroidism; secondary", "Hyperparathyroidism, Secondary", "Hyperparathyroidisms, Secondary", "Secondary hyperparathyroidism NOS", "secondary hyperparathyroidism NOS", "Secondary hyperparathyroidism, NOS", "secondary hyperparathyroidism (disease)", "Secondary hyperparathyroidism (disorder)", "secondary hyperparathyroidism (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary hyperparathyroidism", "shortest_name_length": 29}
{"curie": "MONDO:0020066", "names": ["EDS", "Danlos", "ED syndrome", "elastic skin", "skin elastic", "Ehlers-Danlos", "Danlos disease", "Cutis Elastica", "danlos disease", "cutis elastica", "Cutis elastica", "India rubber skin", "Cutis hyperplastica", "cutis hyperelastica", "Cutis hyperelastica", "CUTIS HYPERELASTICA", "hyperelastica; cutis", "cutis; hyperelastica", "Ehlers Danlos Disease", "Ehlers-Danlos Disease", "ehler danlos syndrome", "Ehler Danlos Syndrome", "Ehlers Danlos syndrome", "ehlers-danlos syndrome", "Ehlers Danlos Syndrome", "Ehlers-Danlos Syndrome", "danlos ehlers syndrome", "Disease, Ehlers-Danlos", "Danlos Disease, Ehlers", "Disease, Ehlers Danlos", "EHLERS-DANLOS SYNDROME", "ehlers danlos syndrome", "Ehlers-Danlos syndrome", "EHLERS DANLOS SYNDROME", "Ehlers-Danlos syndromes", "ehlers danlos syndromes", "Syndrome, Ehlers-Danlos", "eds ehlers danlos syndrome", "Ehlers-Danlos syndrome, NOS", "EDS - Ehlers-Danlos syndrome", "Hereditary collagen dysplasia", "Meekeren-Ehlers-Danlos syndrome", "Ehlers-Danlos syndrome (disorder)", "Dystrophia mesodermalis congenita", "Ehlers-Danlos syndrome (diagnosis)", "Cutis hyperelastica dermatorrhexis", "Ehlers-Danlos syndrome, unspecified", "Fibrodysplasia elastica generalisata", "Dermatorrhexis with dermatochalasis AND arthrochalasis", "DERMATORRHEXIS WITH DERMATOCHALASIS AND ARTHROCHALASIS", "Dermatorrhexis with dermatochalasis and arthrochalasis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ehlers-Danlos syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0011068", "names": ["T1D12", "IDDM12", "TYPE 1 DIABETES MELLITUS 12", "type 1 diabetes mellitus 12", "CTLA4 type 1 diabetes mellitus", "Insulin-Dependent Diabetes Mellitus 12", "INSULIN-DEPENDENT DIABETES MELLITUS 12", "insulin-dependent diabetes mellitus 12", "DIABETES MELLITUS, INSULIN-DEPENDENT, 12", "Diabetes Mellitus, Insulin-Dependent, 12", "diabetes mellitus, insulin-dependent, 12", "diabetes mellitus, insulin-dependent, type 12", "type 1 diabetes mellitus caused by mutation in CTLA4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type 1 diabetes mellitus 12", "shortest_name_length": 5}
{"curie": "UMLS:C3146264", "names": ["Stage IV Prostate Cancer", "Stage IV Prostate Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Prostate Cancer AJCC v7", "shortest_name_length": 24}
{"curie": "MONDO:0013580", "names": ["PDHBD", "pyruvate dehydrogenase E1-BETA deficiency", "PYRUVATE DEHYDROGENASE E1-BETA DEFICIENCY", "Pyruvate dehydrogenase E1-beta deficiency", "pyruvate dehydrogenase E1-beta deficiency", "Pyruvate Dehydrogenase E1-Beta Deficiency", "Pyruvate dehydrogenase complex E1 component subunit beta deficiency", "pyruvate dehydrogenase complex E1 component subunit beta deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyruvate dehydrogenase E1-beta deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0012650", "names": ["NHEJ1-SCID", "NHEJ1 Syndrome", "Nhej1 syndrome", "NHEJ1 SYNDROME", "Cernunnos XLFD", "NHEJ1 deficiency", "Cernunnos deficiency", "Cernunnos-XLF deficiency", "Cernunnos / XLF deficiency", "NHEJ1 (non-homologous end joining factor) syndrome", "Severe Combined Immunodeficiency due to NHEJ1 Deficiency", "Severe combined immunodeficiency due to Cernunnos protein deficiency", "Severe Combined Immunodeficiency With Sensitivity To Ionizing Radiation Due To Nhej1 Deficiency", "severe combined immunodeficiency with sensitivity to ionizing radiation due to Nhej1 deficiency", "SEVERE COMBINED IMMUNODEFICIENCY WITH SENSITIVITY TO IONIZING RADIATION DUE TO NHEJ1 DEFICIENCY", "combined immunodeficiency-microcephaly-growth retardation-sensitivity to ionizing radiation syndrome", "Combined immunodeficiency-microcephaly-growth retardation-sensitivity to ionizing radiation syndrome", "severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation", "Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation", "SEVERE COMBINED IMMUNODEFICIENCY WITH MICROCEPHALY, GROWTH RETARDATION, AND SENSITIVITY TO IONIZING RADIATION", "severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome", "Severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome", "Severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionising radiation syndrome", "Severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome (disorder)", "severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome (diagnosis)", "SCID, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-NEGATIVE, NK CELL-POSITIVE, AND SENSITIVITY TO IONIZING RADIATION DUE TO NHEJ1 DEFICIENCY", "SCID, Autosomal Recessive, T Cell-Negative, B Cell-Negative, NK Cell-Positive, and Sensitivity to Ionizing Radiation due to NHEJ1 Deficiency", "SCID, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive, and sensitivity to ionizing radiation due to Nhej1 deficiency", "SCID, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-NEGATIVE, NK CELL-POSITIVE, WITH MICROCEPHALY, GROWTH RETARDATION, AND SENSITIVITY TO IONIZING RADIATION", "SCID, Autosomal Recessive, T Cell-Negative, B Cell-Negative, NK Cell-Positive, with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation", "SCID, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive, with microcephaly, Growth retardation, and sensitivity to ionizing radiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cernunnos-XLF deficiency", "shortest_name_length": 10}
{"curie": "MONDO:0020588", "names": ["Lung PEComa", "lung PEComa", "lung pecomatous tumor", "Lung PEComatous Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung PEComa", "shortest_name_length": 11}
{"curie": "UMLS:C3897222", "names": ["Untreated Pleomorphic Xanthoastrocytoma", "untreated childhood pleomorphic xanthoastrocytoma", "Untreated Childhood Pleomorphic Xanthoastrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Untreated Childhood Pleomorphic Xanthoastrocytoma", "shortest_name_length": 39}
{"curie": "MONDO:0003845", "names": ["Pericallosal lipoma", "corpus callosum lipoma", "Corpus Callosum Lipoma", "Lipoma of Corpus Callosum", "Lipoma of corpus callosum", "lipoma of corpus callosum", "lipoma of the corpus callosum", "Lipoma of the Corpus Callosum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corpus callosum lipoma", "shortest_name_length": 19}
{"curie": "UMLS:C0555201", "names": ["esthesioneurocytoma", "Esthesioneurocytoma", "Aesthesioneurocytoma", "Olfactory neurocytoma", "Olfactory Neurocytoma", "Esthesioneurocytoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esthesioneurocytoma", "shortest_name_length": 19}
{"curie": "UMLS:C4744309", "names": ["Advanced Extremity Sarcoma", "Advanced Sarcoma of the Extremity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Sarcoma of the Extremity", "shortest_name_length": 26}
{"curie": "MONDO:0043771", "names": ["RADIODERMATITIS", "Radiodermatitis", "radiodermatitis", "Radiodermatitides", "Radiodermatitis, NOS", "Dermatitis radiation", "radiation dermatitis", "Radiation Dermatitis", "dermatitis radiation", "Radiation dermatitis", "dermatitis; radiation", "radiation; dermatitis", "DERMATITIS, RADIATION", "Dermatitis radiation NOS", "Radiation dermatitis, NOS", "radiation recall reaction", "reaction, radiation recall", "radiation recall reactions", "recall reaction, radiation", "radiation recall dermatitis", "reactions, radiation recall", "recall reactions, radiation", "Radiation-Induced Dermatitis", "radiation induced dermatitis", "radiation-induced dermatitis", "dermatitis, radiation recall", "Radiation Induced Dermatitis", "Radiodermatitis, unspecified", "Radiation-induced dermatosis", "Dermatitis, Radiation-Induced", "Dermatitis, Radiation Induced", "radiation recall Dermatitides", "dermatitis, radiation-induced", "dermatitis, radiation induced", "Dermatitides, radiation recall", "Radiation-Induced Dermatitides", "Dermatitis caused by radiation", "radiation-induced Dermatitides", "Dermatitides, radiation-induced", "Dermatitides, Radiation-Induced", "radiation dermatitis (diagnosis)", "radioactive substance; dermatitis", "dermatitis; radioactive substances", "Radiation-induced dermatosis (disorder)", "Dermatitis caused by radiation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radiodermatitis", "shortest_name_length": 15}
{"curie": "UMLS:C0860625", "names": ["Amnestic Disorder Due to a General Medical Condition", "Amnestic disorders due to a general medical condition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Amnestic disorders due to a general medical condition", "shortest_name_length": 52}
{"curie": "MONDO:0800066", "names": ["polydactyly-syndactyly-triphalangism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polydactyly-syndactyly-triphalangism", "shortest_name_length": 36}
{"curie": "MONDO:0004557", "names": ["IFS", "infantile fibrosarcoma", "Infantile Fibrosarcoma", "Infantile fibrosarcoma", "Congenital fibrosarcoma", "infantile; fibrosarcoma", "Congenital Fibrosarcoma", "fibrosarcoma; infantile", "congenital fibrosarcoma", "fibrosarcoma; congenital", "congenital; fibrosarcoma", "Infantile fibrosarcoma (disorder)", "infantile fibrosarcoma (diagnosis)", "infantile fibrosarcoma (congenital fibrosarcoma)", "infantile fibrosarcoma (morphologic abnormality)", "Infantile fibrosarcoma (congenital fibrosarcoma)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital fibrosarcoma", "shortest_name_length": 3}
{"curie": "UMLS:C5667243", "names": ["Recurrent Schwannoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Schwannoma", "shortest_name_length": 20}
{"curie": "UMLS:C4683664", "names": ["Small Lymphocytic Lymphoma by Ann Arbor Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Lymphocytic Lymphoma by Ann Arbor Stage", "shortest_name_length": 45}
{"curie": "MONDO:0034121", "names": ["PEBEL2", "CARKD deficiency", "NAD(P)HX dehydratase deficiency", "NAD(P)HX dehydratase deficiency (disorder)", "ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "NAD(P)HX dehydratase deficiency", "shortest_name_length": 6}
{"curie": "UMLS:C4329644", "names": ["Cerebellar and Fourth Ventricle Ependymal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebellar and Fourth Ventricle Ependymal Tumor", "shortest_name_length": 47}
{"curie": "UMLS:C5204284", "names": ["Diffuse Large B-Cell Lymphoma in Partial Remission"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse Large B-Cell Lymphoma in Partial Remission", "shortest_name_length": 50}
{"curie": "MONDO:0032608", "names": ["MC1DN3", "nuclear type mitochondrial complex I deficiency 3", "mitochondrial complex 1 deficiency, nuclear type 3", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 3", "shortest_name_length": 6}
{"curie": "MONDO:0035562", "names": ["acquired human prion disease", "infectious human prion disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired human prion disease", "shortest_name_length": 28}
{"curie": "MONDO:0010052", "names": ["SPGF4", "RPRGL4", "Aspermatogenesis", "aspermatogenesis", "SYCP3 azoospermia", "Spermatogenic arrest", "spermatogenesis arrest", "Spermatogenesis arrest", "SPERMATOGENESIS ARREST", "arrest; spermatogenesis", "spermatogenic failure 4", "spermatogenesis; arrest", "SPERMATOGENIC FAILURE 4", "Spermatogenic failure 4", "SPERMATOGENESIS ARRESTED", "Spermatogenesis arrested", "Arrest of spermatogenesis", "Spermatogenic arrest, NOS", "arrest of spermatogenesis", "Spermatogenesis arrest, NOS", "spermatogenic failure type 4", "PREGNANCY LOSS, RECURRENT, 4", "pregnancy loss, recurrent, 4", "Spermatogenic arrest (finding)", "AZOOSPERMIA WITH MATURATION ARREST", "azoospermia with maturation arrest", "Azoospermia With Maturation Arrest", "azoospermia caused by mutation in SYCP3", "AZOOSPERMIA DUE TO PERTURBATIONS OF MEIOSIS", "Azoospermia Due To Perturbations Of Meiosis", "azoospermia due to Perturbations of meiosis", "pregnancy loss, recurrent, susceptibility to, 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 4", "shortest_name_length": 5}
{"curie": "MONDO:0035942", "names": ["B-lymphoblastic leukemia/lymphoma with t(12;21)(p13.2;q22.1)", "B lymphoblastic leukemia lymphoma with t(12;21)(p13;q22); TEL-AML1", "B Lymphoblastic Leukemia/Lymphoma with t(12;21)(p13.2;q22.1); ETV6-RUNX1", "B-lymphoblastic leukemia/lymphoma with t(12;21)(p13.2;q22.1); ETV6-RUNX1", "B Lymphoblastic Leukemia/Lymphoma with t(12;21)(p13;q22); TEL-AML1 (ETV6-RUNX1)", "B lymphoblastic leukemia/lymphoma with t(12;21)(p13;q22); TEL-AML1 (ETV6-RUNX1)", "B lymphoblastic leukemia lymphoma with t(12;21)(p13;q22); TEL-AML1 (ETV6-RUNX1)", "B-Lymphoblastic Leukemia/Lymphoma with t(12;21)(p13;q22); TEL-AML1 (ETV6-RUNX1)", "B lymphoblastic leukaemia lymphoma with t(12;21)(p13;q22); TEL-AML1 (ETV6-RUNX1)", "B lymphoblastic leukemia lymphoma with t(12;21) (p13;q22); TEL/AML1 (ETV6-RUNX1)", "B lymphoblastic leukaemia lymphoma with t(12;21) (p13;q22); TEL/AML1 (ETV6-RUNX1)", "B lymphoblastic leukemia lymphoma with t(12;21) (p13;q22); TEL/AML1 (ETV6-RUNX1) (disorder)", "B lymphoblastic leukemia lymphoma with t(12;21) (p13;q22); TEL/AML1 (ETV6-RUNX1) (diagnosis)", "B lymphoblastic leukemia lymphoma with t(12;21)(p13;q22); TEL-AML1 (ETV6-RUNX1) (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-lymphoblastic leukemia/lymphoma with t(12;21)(p13.2;q22.1)", "shortest_name_length": 60}
{"curie": "UMLS:C1336810", "names": ["Transplant-Related Hematologic Malignancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transplant-Related Hematologic Malignancy", "shortest_name_length": 41}
{"curie": "UMLS:C0153792", "names": ["Stage III Hodgkin Lymphoma", "Hodgkin's Disease Stage III", "Stage III Hodgkin's Disease", "Hodgkin's disease stage III", "Hodgkin's Lymphoma Stage III", "Stage III Hodgkin's Lymphoma", "Hodgkin's disease NOS stage III", "Ann Arbor Stage III Hodgkin Lymphoma", "Hodgkin disease of lymph nodes of multiple sites", "Hodgkin's disease of lymph nodes of multiple sites", "Hodgkin's disease, NOS of lymph nodes of multiple sites", "Hodgkin's disease of lymph nodes of multiple sites (disorder)", "Hodgkin's disease, unspecified type, lymph nodes of multiple sites", "Hodgkin's disease, unspecified type, involving lymph nodes of multiple sites"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Hodgkin Lymphoma", "shortest_name_length": 26}
{"curie": "MONDO:0016085", "names": ["Cole Carpenter syndrome", "Cole-Carpenter Syndrome", "Cole-Carpenter syndrome", "Cole-Carpenter dysplasia", "Cole-Carpenter dysplasia (disorder)", "bone fragility-craniosynostosis-proptosis-hydrocephalus syndrome", "Bone fragility-craniosynostosis-proptosis-hydrocephalus syndrome", "Bone fragility, craniosynostosis, proptosis, hydrocephalus syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cole-Carpenter syndrome", "shortest_name_length": 23}
{"curie": "UMLS:C1096642", "names": ["plant allergy", "allergy plant", "allergy plants", "Herbal allergy", "plants allergy", "allergy; plants", "allergies plant", "plants; allergy", "allergies plants", "Allergy to plant", "Allergy to plants"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Allergy to plant", "shortest_name_length": 13}
{"curie": "MONDO:0005537", "names": ["Perianal Crohn disease", "perianal Crohn disease", "Perianal Crohn's disease", "Crohn's disease perianal", "perianal Crohn's disease", "Perianal Crohn's disease (disorder)", "Crohn's disease perianal (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "perianal Crohn disease", "shortest_name_length": 22}
{"curie": "UMLS:C0280143", "names": ["Stage II", "stage II grade 1 follicular lymphoma", "Stage II Grade 1 Follicular Lymphoma", "Grade I Follicular Lymphoma Stage II", "Stage II Grade I Follicular Lymphoma", "Ann Arbor Stage II Grade 1 Follicular Lymphoma", "Follicular Small Cleaved Cell Lymphoma Stage II", "stage II follicular small cleaved cell lymphoma", "Stage II Follicular Small Cleaved Cell Lymphoma", "follicular small cleaved cell lymphoma, stage II", "stage II grade I follicular small cleaved cell lymphoma", "Stage II Grade I Follicular Small Cleaved Cell Lymphoma", "Grade I Follicular Small Cleaved Cell Lymphoma Stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage II Grade 1 Follicular Lymphoma", "shortest_name_length": 8}
{"curie": "UMLS:C2827454", "names": ["Childhood Renal Disorder", "Pediatric Kidney Disease", "Childhood Kidney Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Kidney Disorder", "shortest_name_length": 24}
{"curie": "MONDO:0019869", "names": ["Mosaic trisomy 22", "mosaic trisomy 22", "Trisomy mosaic 22", "Trisomy 22 mosaic", "trisomy 22 mosaicism", "Trisomy 22 mosaicism", "Mosaic trisomy type 22", "Mosaic trisomy 22 syndrome", "Mosaic trisomy chromosome 22", "Chromosome 22 trisomy mosaic", "Trisomy 22 mosaicism syndrome", "trisomy 22 mosaicism (diagnosis)", "Mosaic trisomy 22 syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mosaic trisomy 22", "shortest_name_length": 17}
{"curie": "MONDO:0012419", "names": ["ARMD7", "age related macular degeneration 7", "MACULAR DEGENERATION, AGE-RELATED, 7", "macular degeneration, age-related, 7", "Macular Degeneration, Age-Related, 7", "HTRA1 age-related macular degeneration", "age related macular degeneration type 7", "macular Degeneration, age-related, type 7", "macular degeneration, age-related, neovascular type", "age-related macular degeneration caused by mutation in HTRA1", "macular Degeneration, age-related, wet type, susceptibility to", "MACULAR DEGENERATION, AGE-RELATED, WET TYPE, SUSCEPTIBILITY TO", "MACULAR DEGENERATION, AGE-RELATED, NEOVASCULAR TYPE, SUSCEPTIBILITY TO", "macular Degeneration, age-related, neovascular type, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "age related macular degeneration 7", "shortest_name_length": 5}
{"curie": "UMLS:C5420849", "names": ["Pseudoadenomatous Hyperplasia of the Ciliary Body", "Reactive Epithelial Hyperplasia of the Ciliary Body", "Pseudoadenomatous Hyperplasia of the Ciliary Body Epithelium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reactive Epithelial Hyperplasia of the Ciliary Body", "shortest_name_length": 49}
{"curie": "MONDO:0020762", "names": ["DMJDS2", "DIENCEPHALIC-MESENCEPHALIC JUNCTION DYSPLASIA SYNDROME 2", "diencephalic-mesencephalic junction dysplasia syndrome 2", "SPASTIC TETRAPARESIS, DYSTONIA, DEVELOPMENTAL DELAY, AND STRUCTURAL ABNORMALITIES OF THE BASAL GANGLIA", "spastic tetraparesis, dystonia, developmental delay, and structural abnormalities of the basal ganglia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diencephalic-mesencephalic junction dysplasia syndrome 2", "shortest_name_length": 6}
{"curie": "UMLS:C4521967", "names": ["Stage II Lung Cancer", "Stage II Lung Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Lung Cancer AJCC v7", "shortest_name_length": 20}
{"curie": "UMLS:C1879641", "names": ["Adnexal Mucinous Carcinoma", "Sweat Gland Mucinous Carcinoma", "Adnexal Mucinous Adenocarcinoma", "Primary Cutaneous Mucinous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Cutaneous Mucinous Carcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0010692", "names": ["nRNA", "NUCLEAR RIBONUCLEIC ACID", "nuclear ribonucleic acid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nuclear ribonucleic acid", "shortest_name_length": 4}
{"curie": "UMLS:C5206637", "names": ["Warty PeIN", "Warty (Bowenoid) PeIN", "Warty Penile Intraepithelial Neoplasia", "Warty (Bowenoid) Penile Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Warty (Bowenoid) Penile Intraepithelial Neoplasia", "shortest_name_length": 10}
{"curie": "MONDO:0014038", "names": ["CRCS12", "POLE colorectal cancer", "susceptibility to colorectal cancer 12", "COLORECTAL CANCER, SUSCEPTIBILITY TO, 12", "colorectal cancer, susceptibility to, 12", "colorectal cancer caused by mutation in POLE", "colorectal cancer, susceptibility to, type 12", "COLORECTAL CANCER, SUSCEPTIBILITY TO, ON CHROMOSOME 12q24", "colorectal cancer, susceptibility to, on chromosome 12Q24"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorectal cancer, susceptibility to, 12", "shortest_name_length": 6}
{"curie": "MONDO:0011341", "names": ["microcephaly, facial abnormalities, micromelia, and mental retardation", "Microcephaly, Facial Abnormalities, Micromelia, and Mental Retardation", "MICROCEPHALY, FACIAL ABNORMALITIES, MICROMELIA, AND MENTAL RETARDATION", "microcephaly, facial abnormalities, micromelia, and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly, facial abnormalities, micromelia, and intellectual disability", "shortest_name_length": 70}
{"curie": "MONDO:0018684", "names": ["neonatal cardiac dysrhythmia", "Idiopathic neonatal atrial flutter", "idiopathic neonatal atrial flutter", "Idiopathic neonatal atrial flutter (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic neonatal atrial flutter", "shortest_name_length": 28}
{"curie": "MONDO:0009694", "names": ["MPOD", "MPO Deficiency", "MPO DEFICIENCY", "MPO deficiency", "MYELOPEROXIDASE DEFICIENCY", "Myeloperoxidase Deficiency", "deficiency myeloperoxidase", "myeloperoxidase deficiency", "Myeloperoxidase deficiency", "MPO - Myeloperoxidase deficiency", "Myeloperoxidase deficiency syndrome", "Myeloperoxidase deficiency (disorder)", "Myeloperoxidase deficiency (diagnosis)", "Myeloperoxidase deficiency syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myeloperoxidase deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0008750", "names": ["Castro Gago-Pombo-Novo syndrome", "Castro Gago Pombo Novo syndrome", "albinism-microcephaly digital anomalies syndrome", "ALBINISM-MICROCEPHALY-DIGITAL ANOMALIES SYNDROME", "Microcephaly-Albinism-Digital Anomalies Syndrome", "Albinism-Microcephaly-Digital Anomalies Syndrome", "albinism-microcephaly-digital anomalies syndrome", "Microcephaly-albinism-digital anomalies syndrome", "microcephaly-albinism-digital anomalies syndrome", "Albinism-Microcephaly digital anomalies syndrome", "MICROCEPHALY-ALBINISM-DIGITAL ANOMALIES SYNDROME", "Microcephaly albinism digital anomalies syndrome", "Microcephaly with albinism and digital anomaly syndrome", "Microcephalus with albinism and digital anomaly syndrome", "Microcephalus with albinism and digital anomaly syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly-albinism-digital anomalies syndrome", "shortest_name_length": 31}
{"curie": "MONDO:0016352", "names": ["idiopathic hypercalciuria", "idiopathic inherited hypercalciuria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic inherited hypercalciuria", "shortest_name_length": 25}
{"curie": "MONDO:0033938", "names": ["Acute radiation disease", "acute radiation syndrome", "Acute radiation syndrome", "Acute Radiation Syndrome", "Acute radiation sickness", "Radiation Syndrome, Acute", "Acute Radiation Syndromes", "Radiation Syndromes, Acute", "Acute radiation disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute radiation syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0001933", "names": ["pancreatic islet disorder", "Pancreas (endocrine only)", "Endocrine Pancreas Disease", "pancreatic islet disorders", "endocrine pancreas disease", "Endocrine Pancreas Disorder", "endocrine pancreas disorder", "Disease of endocrine pancreas", "disorder of pancreatic islets", "disease of endocrine pancreas", "Disorder of pancreatic islets", "Endocrine pancreatic disorder", "disorder of endocrine pancreas", "Diseases of Endocrine Pancreas", "Disorder of endocrine pancreas", "Disease of islets of Langerhans", "disorder of islets of langerhans", "Disorder of islets of Langerhans", "Endocrine pancreatic disorder NOS", "Disorder of pancreatic islets, NOS", "Disease of endocrine pancreas, NOS", "Disorder of endocrine pancreas, NOS", "Disorder of islets of Langerhans, NOS", "endocrine pancreas disease or disorder", "disease or disorder of endocrine pancreas", "Disorder of endocrine pancreas (disorder)", "disorder of endocrine pancreas (diagnosis)", "pancreatic internal secretion disorder other", "Other disorders of pancreatic internal secretion", "Other disorders of pancreatic internal secretion (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endocrine pancreas disorder", "shortest_name_length": 25}
{"curie": "MONDO:0700055", "names": ["KAND", "KIF1A neurological disorder", "KIF1A related neurological disorder", "neurological disorder caused by mutation in KIF1A", "neurological disorder caused by variation in KIF1A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "KIF1A related neurological disorder", "shortest_name_length": 4}
{"curie": "MONDO:0007566", "names": ["MSSE", "ESS1", "ESS1, FORMERLY", "ESS1, formerly", "ESS1 (formerly)", "Ferguson-Smith tumor", "Ferguson-Smith Tumor", "Ferguson-Smith tumour", "Ferguson-Smith disease", "Familial keratoacanthoma", "Keratoacanthoma familial", "Multiple keratoacanthoma", "Hereditary keratoacanthoma", "Ferguson-Smith type epithelioma", "FERGUSON-SMITH-TYPE EPITHELIOMA", "Ferguson-Smith-type epithelioma", "Ferguson-Smith Type epithelioma", "Multiple familial keratoacanthoma", "Hereditary keratoacanthoma (disorder)", "Epithelioma, self-healing squamous, 1", "Self-healing squamous epithelioma type 1", "self-healing squamous epithelioma type 1", "multiple self-healing squamous epithelioma", "multiple self healing squamous epithelioma", "Multiple self-healing squamous epithelioma", "Multiple keratoacanthoma, Ferguson-Smith type", "multiple keratoacanthoma, Ferguson-Smith type", "multiple self-healing epithelioma of Ferguson-Smith", "Multiple Self Healing Epithelioma of Ferguson-Smith", "Multiple self-healing epithelioma of Ferguson-Smith", "multiple self healing epithelioma of Ferguson-Smith", "multiple self-healing squamous epithelioma, susceptibility to", "MULTIPLE SELF-HEALING SQUAMOUS EPITHELIOMA, SUSCEPTIBILITY TO", "Multiple self-healing epithelioma of Ferguson-Smith (disorder)", "Familial primary self-healing squamous epithelioma of the skin, Ferguson-Smith type", "familial primary self-healing squamous epithelioma of the skin, Ferguson-Smith type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple self-healing squamous epithelioma", "shortest_name_length": 4}
{"curie": "MONDO:0014081", "names": ["IMD11", "IMD11A", "CARD11 deficiency", "immunodeficiency 11", "IMMUNODEFICIENCY 11", "immunodeficiency 11A", "CARD11 IMMUNODEFICIENCY", "CARD11 immunodeficiency", "immunodeficiency type 11", "SCID due to CARD11 deficiency", "severe combined immunodeficiency due to CARD11 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe combined immunodeficiency due to CARD11 deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C3899661", "names": ["Gastric (Stomach) Cancer", "Childhood Gastric Carcinoma", "Childhood Carcinoma of the Stomach"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Gastric Carcinoma", "shortest_name_length": 24}
{"curie": "MONDO:0015988", "names": ["MCDK", "Multicystic kidney", "Multicystic Kidney", "multicystic kidney", "Multicystic kidneys", "Multicystic Kidneys", "multicystic kidneys", "Multicystic Renal Dysplasia", "Multicystic renal dysplasia", "multicystic renal dysplasia", "multicystic kidney dysplasia", "Dysplasia, Multicystic Renal", "Multicystic kidney dysplasia", "Multicystic Renal Dysplasias", "Renal Dysplasia, Multicystic", "Multicystic Kidney Dysplasia", "Dysplasia, Multicystic Kidney", "Multicystic Dysplastic Kidney", "Kidney Dysplasia, Multicystic", "Dysplasias, Multicystic Renal", "Multicystic Kidney Dysplasias", "multicystic dysplastic kidney", "Multicystic dysplastic kidney", "Renal Dysplasias, Multicystic", "Multicystic Dysplastic Kidneys", "multicystic dysplastic kidneys", "Multicystic dysplastic kidneys", "Kidney Dysplasias, Multicystic", "Dysplasias, Multicystic Kidney", "MCKD - Multicystic kidney disease", "Multicystic renal dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multicystic dysplastic kidney", "shortest_name_length": 4}
{"curie": "UMLS:C0854268", "names": ["fetal damage", "Fetal damage", "Foetal damage", "Fetal damage NOS", "Foetal damage NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fetal damage", "shortest_name_length": 12}
{"curie": "MONDO:0009734", "names": ["HHF1", "hyperinsulinism, congenital", "Nesidioblastosis of pancreas", "familial hyperinsulinemic hypoglycemia 1", "Familial Hyperinsulinemic Hypoglycemia 1", "Hyperinsulinemic hypoglycemia, familial, 1", "Hyperinsulinemic Hypoglycemia, Familial, 1", "hypoglycemia, hyperinsulinemic, of infancy", "HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 1", "hyperinsulinemic hypoglycemia, familial, 1", "ABCC8 hyperinsulinemic hypoglycemia (disease)", "hyperinsulinemic hypoglycemia, familial, type 1", "persistent hyperinsulinemic hypoglycemia of infancy", "hyperinsulinemic hypoglycemia due to SUR1 deficiency", "hyperinsulinism, familial, with pancreatic Nesidioblastosis", "Hyperinsulinemic Hypoglycemia Due to Focal Adenomatous Hyperplasia", "hyperinsulinemic hypoglycemia due to focal adenomatous hyperplasia", "HYPERINSULINEMIC HYPOGLYCEMIA DUE TO FOCAL ADENOMATOUS HYPERPLASIA", "hyperinsulinemic hypoglycemia (disease) caused by mutation in ABCC8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperinsulinemic hypoglycemia, familial, 1", "shortest_name_length": 4}
{"curie": "MONDO:0013355", "names": ["CDAN4", "CDA IV", "CDA type 4", "CDA, type 4", "CDA type IV", "CDA, TYPE IV", "CDA due to KLF1 mutation", "Congenital dyserythropoietic anemia type 4", "congenital dyserythropoietic anemia type 4", "Congenital dyserythropoietic anaemia type 4", "Congenital dyserythropoietic anemia type IV", "congenital dyserythropoietic anemia type IV", "Congenital Dyserythropoietic Anemia Type IV", "Congenital dyserythropoietic anaemia type IV", "anemia, congenital dyserythropoietic, type 4", "congenital dyserythropoietic anaemia type IV", "ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IV", "anemia, congenital dyserythropoietic, type IV", "dyserythropoietic anemia, congenital, type IV", "Congenital dyserythropoietic anemia type IV (disorder)", "Congenital dyserythropoietic anemia due to KLF1 mutation", "congenital dyserythropoietic anemia due to KLF1 mutation", "Congenital dyserythropoietic anaemia due to KLF1 mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital dyserythropoietic anemia type 4", "shortest_name_length": 5}
{"curie": "MONDO:0015569", "names": ["apertura pyriformis with holoprosencephaly", "congenital nasal pyriform aperture stenosis with holoprosencephaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital nasal pyriform aperture stenosis with holoprosencephaly", "shortest_name_length": 42}
{"curie": "UMLS:C2986670", "names": ["Stage III Liver Cancer", "stage IIIA adult primary liver cancer", "Stage IIIA Adult Liver Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Adult Liver Cancer AJCC v7", "shortest_name_length": 22}
{"curie": "DOID:0060172", "names": ["juvenile absence epilepsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile absence epilepsy", "shortest_name_length": 25}
{"curie": "UMLS:C1336909", "names": ["Endometrial Endometrioid Adenocarcinoma with Metaplastic Changes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endometrial Endometrioid Adenocarcinoma with Metaplastic Changes", "shortest_name_length": 64}
{"curie": "MONDO:0007820", "names": ["Double tooth", "Teeth, double", "'DOUBLE TOOTH'", "'Double Tooth'", "Twinning tooth", "Conjoined teeth", "Fused Mandibular Incisor", "Fused mandibular incisors", "fused mandibular incisors", "Mandibular Incisor, Fused", "Incisor, Fused Mandibular", "Fused Mandibular Incisors", "Mandibular Incisors, Fused", "Incisors, Fused Mandibular", "incisors, FUSED mandibular", "INCISORS, FUSED MANDIBULAR", "Fusion of mandibular incisor teeth", "Fusion of mandibular incisor teeth (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fused mandibular incisors", "shortest_name_length": 12}
{"curie": "MONDO:0001407", "names": ["Ca trachea", "trachea cancer", "tracheal cancer", "Tracheal cancer", "cancer tracheal", "cancer of trachea", "tracheal neoplasm", "Neoplasm malig;trachea", "CA - Cancer of trachea", "malignant trachea tumor", "Malignant Trachea Tumor", "Malignant Tracheal Tumor", "Malignant tracheal tumor", "TRACHEA CANCER MALIGNANT", "malignant tracheal tumor", "Malignant tracheal tumour", "Malignant Tumor of Trachea", "malignant tumor of trachea", "malignant trachea neoplasm", "Malignant Trachea Neoplasm", "Malignant tumor of trachea", "Malignant Tracheal Neoplasm", "tracheal cancer (diagnosis)", "Malignant tumour of trachea", "malignant tracheal neoplasm", "Malignant Neoplasm of Trachea", "malignant neoplasm of trachea", "Malignant neoplasm of trachea", "malignant tumor of the trachea", "Malignant Tumor of the Trachea", "Malignant Neoplasm of the Trachea", "malignant neoplasm of the trachea", "malignant neosplasm of the trachea", "Malignant tumor of trachea (disorder)", "malignant neoplasm of trachea (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tracheal cancer", "shortest_name_length": 10}
{"curie": "MONDO:0020743", "names": ["MPAL", "Acute mixed lineage leukemia", "Acute mixed lineage leukaemia", "mixed phenotype acute leukemia", "Mixed Phenotype Acute Leukemia", "Mixed phenotype acute leukemia", "Mixed phenotype acute leukaemia", "MPAL - mixed phenotype acute leukemia", "MPAL - mixed phenotype acute leukaemia", "Mixed phenotype acute leukemia (disorder)", "mixed phenotype acute leukemia (diagnosis)", "Mixed phenotype (biphenotypic) acute leukemia", "Mixed phenotype acute leukemia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed phenotype acute leukemia", "shortest_name_length": 4}
{"curie": "UMLS:C4288009", "names": ["Vulvar Fibrolipoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Fibrolipoma", "shortest_name_length": 18}
{"curie": "MONDO:0001671", "names": ["mucocele appendix", "appendix mucocele", "appendix; mucocele", "mucocele; appendix", "Appendiceal mucocele", "Appendicele mucocele", "Appendicele Mucocele", "Appendiceal Mucocele", "mucocele of appendix", "Mucocele of appendix", "appendiceal mucocele", "Mucocele of Appendix", "Appendicular mucocele", "Mucocoele of appendix", "Appendiceal mucocoele", "mucocele of the appendix", "Mucocele of the Appendix", "Mucocele of appendix (disorder)", "mucocele of appendix (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucocele of appendix", "shortest_name_length": 17}
{"curie": "UMLS:C4526907", "names": ["Stage IV Soft Tissue Sarcoma of the Trunk and Extremities", "Stage IV Soft Tissue Sarcoma of the Trunk and Extremities AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Soft Tissue Sarcoma of the Trunk and Extremities AJCC v8", "shortest_name_length": 57}
{"curie": "UMLS:C1512433", "names": ["High-Grade CIN", "HSIL of Cervix", "High-Grade Cervical SIL", "Cervical high grade squamous intraepithelial lesion", "High-Grade Cervical Squamous Intraepithelial Lesion", "High Grade Cervical Squamous Intraepithelial Lesion", "High Grade Cervical Squamous Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical high grade squamous intraepithelial lesion", "shortest_name_length": 14}
{"curie": "UMLS:C0334050", "names": ["adenose", "ADENOSES", "ADENOSIS", "adenosis", "Adenosis", "Adenoses", "Adenosis, NOS", "Adenosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenosis", "shortest_name_length": 7}
{"curie": "MONDO:0006500", "names": ["Angioma", "angioma", "Hemangioma", "hemangioma", "HEMANGIOMA", "hemangiomas", "Hemangiomas", "Haemangioma", "Angioma NOS", "haemangioma", "Angioma, NOS", "haemangiomas", "Hemangiomata", "Hemangioma NOS", "Benign angioma", "Benign Angioma", "benign angioma", "Hemangioma, NOS", "Strawberry mark", "Haemangioma NOS", "Haemangioma, NOS", "benign hemangioma", "Benign hemangioma", "Benign Hemangioma", "HEMANGIOMA, BENIGN", "hemangioma, benign", "Benign haemangioma", "benign hemangiomas", "Hemangioma, any site", "Hemangioma (disorder)", "Haemangioma, any site", "hemangioma (diagnosis)", "Hemangioma - morphology", "Haemangioma - morphology", "Hemangioma unspecified site", "Hemangioma, unspecified site", "Haemangioma, unspecified site", "hemangioma (physical finding)", "Hemangioma of unspecified site", "Haemangioma of unspecified site", "Benign hemangioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemangioma", "shortest_name_length": 7}
{"curie": "MONDO:0008280", "names": ["PJS", "Peutz's syndrome", "Peutz's Syndrome", "Peutz Jeghers polyp", "peutz-jegher syndrome", "peutz jegher syndrome", "Peutz-Jegher Syndrome", "Peutz-Jeghers Disease", "Perioral Lentiginoses", "Perioral Lentiginosis", "Perioral lentiginosis", "Jeghers-Peutz syndrome", "Peutz-Jeghers syndrome", "PEUTZ-JEGHERS SYNDROME", "peutz-jeghers syndrome", "lentiginosis, perioral", "Peutz-Jeghers Syndrome", "Peutz Jeghers Syndrome", "Lentiginoses, Perioral", "syndrome peutz-jeghers", "peutz jeghers syndrome", "Peutz Jeghers syndrome", "Lentiginosis, Perioral", "Jeghers-Peutz Syndrome", "peutz-jegher's syndrome", "Peutz Jeghers Polyposis", "peutz jeghers syndromes", "Peutz Jeghers polyposis", "Syndrome, Peutz-Jeghers", "Peutz-Jegher's Syndrome", "Peutz Jegher's Syndrome", "Peutz-Jeghers Polyposis", "Peutz-Jeghers polyposis", "Peutz-Jeghers' syndrome", "Polyposis, Peutz-Jeghers", "Syndrome, Peutz-Jegher's", "polyps-and-Spots syndrome", "Polyps-and-Spots Syndrome", "POLYPOSIS, INTESTINAL, II", "polyps and spots syndrome", "Polyps and Spots Syndrome", "Peutz Jeghers colon polyp", "POLYPS-AND-SPOTS SYNDROME", "Syndrome, Polyps-and-Spots", "Polyps-and-Spots Syndromes", "Colonic hamartomatous polyp", "colonic hamartomatous polyp", "gastric Peutz-Jeghers polyp", "Syndromes, Polyps-and-Spots", "PJS - Peutz-Jehgers syndrome", "PJS - Peutz-Jeghers syndrome", "Peutz-Jeghers syndrome (disorder)", "Hamartomatous Intestinal Polyposis", "hamartomatous intestinal polyposis", "Hamartomatous intestinal polyposis", "Peutz-Jeghers syndrome (diagnosis)", "Hamartomatous Intestinal Polyposes", "Peutz-Jeghers small bowel hamartoma", "periorificial lentiginosis syndrome", "polyposis, hamartomatous intestinal", "Polyposes, Hamartomatous Intestinal", "Periorificial Lentiginosis Syndrome", "Intestinal Polyposis, Hamartomatous", "Polyposis, Hamartomatous Intestinal", "Periorificial lentiginosis syndrome", "peutz-jeghers small bowel hamartoma", "Intestinal Polyposes, Hamartomatous", "Peutz-Jeghers Small Bowel Hamartoma", "POLYPOSIS, HAMARTOMATOUS INTESTINAL", "Peutz-Jeghers polyps of small bowel", "Periorificial Lentiginosis Syndromes", "Syndrome, Periorificial Lentiginosis", "Syndromes, Periorificial Lentiginosis", "Peutz-Jeghers polyp of small intestine", "Peutz-Jeghers Polyp of Small Intestine", "Peutz-Jeghers polyp of small Intestine", "Peutz-Jeghers Hamartoma of Small Bowel", "Peutz-Jeghers Small Intestine Hamartoma", "hereditary intestinal polyposis syndrome", "Peutz-Jeghers Hamartoma of the Small Bowel", "Peutz-Jeghers Polyp of the Small Intestine", "Peutz-Jeghers Harmatoma of Small Intestine", "Peutz-Jeghers Hamartoma of Small Intestine", "Peutz-Jeghers Harmatoma of the Small Intestine", "Peutz-Jeghers polyps of small bowel (disorder)", "Peutz-Jeghers Hamartoma of the Small Intestine", "INTESTINAL POLYPOSIS-CUTANEOUS PIGMENTATION SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peutz-Jeghers syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0011327", "names": ["NIID", "Niid", "neuronal intranuclear inclusion disease", "Neuronal intranuclear inclusion disease", "NEURONAL INTRANUCLEAR INCLUSION DISEASE", "Neuronal Intranuclear Inclusion Disease", "neuronal intranuclear hyaline inclusion disease", "Neuronal intranuclear inclusion disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuronal intranuclear inclusion disease", "shortest_name_length": 4}
{"curie": "UMLS:C0022865", "names": ["Labor Complication", "Labor complication", "labor complication", "complications labor", "labor complications", "Labor Complications", "Complication, Labor", "Labour complication", "Complications, Labor", "Complication of labor", "Complication of labor NOS", "Complication of labour NOS", "Obstetric Labor Complication", "Complication, Obstetric Labor", "Obstetric Labor Complications", "Labor Complication, Obstetric", "Labor Complications, Obstetric", "Complications, Obstetric Labor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Obstetric Labor Complications", "shortest_name_length": 18}
{"curie": "MONDO:0030906", "names": ["Trichomonas tenax trichomoniasis", "Trichomonas tenax infectious disease", "Trichomonas tenax disease or disorder", "Trichomonas tenax caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Trichomonas tenax infectious disease", "shortest_name_length": 32}
{"curie": "UMLS:C3273119", "names": ["Gallbladder NET G1", "Gallbladder Carcinoid Tumor", "Gallbladder Neuroendocrine Tumor G1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gallbladder Neuroendocrine Tumor G1", "shortest_name_length": 18}
{"curie": "UMLS:C0280166", "names": ["Stage III Burkitt Lymphoma", "stage III adult Burkitt lymphoma", "Stage III Adult Burkitt Lymphoma", "Stage III Adult Burkitt's Lymphoma", "Ann Arbor Stage III Adult Burkitt Lymphoma", "adult small noncleaved cell lymphoma, stage III", "Stage III Adult Diffuse Small Non-Cleaved Cell Lymphoma", "Adult Diffuse Small Non-Cleaved Cell Lymphoma Stage III", "stage III adult diffuse small noncleaved cell/Burkitt's lymphoma", "Adult Diffuse Small Non-Cleaved Cell/Burkitt's Lymphoma Stage III", "Stage III Adult Diffuse Small Non-Cleaved Cell/Burkitt's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Adult Burkitt Lymphoma", "shortest_name_length": 26}
{"curie": "MONDO:0017471", "names": ["Congenital patella dislocation", "congenital patella dislocation", "Congenital patellar dislocation", "congenital patellar dislocation", "patella; dislocation, congenital", "dislocation; patella, congenital", "Congenital dislocation of patella", "congenital dislocation of the patella", "Congenital dislocation of the patella", "Congenital dislocation of patella (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital patella dislocation", "shortest_name_length": 30}
{"curie": "MONDO:0004817", "names": ["Nonsecretory myeloma", "Non-secretory myeloma", "non-secreting myeloma", "non-secretory myeloma", "non-functioning myeloma", "Non-Secretory Multiple Myeloma", "non-secretory multiple myeloma", "Non-secretory myeloma (disorder)", "non-secretory plasma cell myeloma", "Non-secretory myeloma (diagnosis)", "Non-Secretory Plasma Cell Myeloma", "malignant neoplasm multiple myeloma non-secretory"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-secretory plasma cell myeloma", "shortest_name_length": 20}
{"curie": "MONDO:0011039", "names": ["AMVC", "VARIOLIFORM MACULAR ATROPHY OF THE SKIN", "varioliform macular atrophy of the skin", "Varioliform Macular Atrophy of the Skin", "atrophia maculosa varioliformis cutis, familial", "ATROPHIA MACULOSA VARIOLIFORMIS CUTIS, FAMILIAL", "Atrophia Maculosa Varioliformis Cutis, Familial", "atrophia MACULOSA VARIOLIFORMIS cutis, familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrophia maculosa varioliformis cutis, familial", "shortest_name_length": 4}
{"curie": "MONDO:0006428", "names": ["Diffuse large B-cell lymphoma, spleen", "splenic diffuse large B-cell lymphoma", "Splenic Diffuse Large B-Cell Lymphoma", "large B-cell diffuse lymphoma of spleen", "Primary Splenic Diffuse Large B-Cell Lymphoma", "primary splenic diffuse large B-cell lymphoma", "large B-cell diffuse lymphoma of spleen (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "splenic diffuse large B-cell lymphoma", "shortest_name_length": 37}
{"curie": "MONDO:0005978", "names": ["Theileriosis", "theileriosis", "Theileriases", "theileriasis", "Theilerioses", "Theileriasis", "Infection by Theileria", "infection by Theileria", "Infection by Theileria, NOS", "Infection caused by Theileria", "Infection caused by Theileria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "theileriasis", "shortest_name_length": 12}
{"curie": "MONDO:0002485", "names": ["breast NET", "Breast Endocrine Neoplasm", "breast endocrine neoplasm", "breast neuroendocrine tumor", "Breast Neuroendocrine Neoplasm", "breast neuroendocrine neoplasm", "neuroendocrine neoplasm of breast", "Neuroendocrine Neoplasm of Breast", "neuroendocrine tumor of the breast", "Neuroendocrine Neoplasm of the Breast", "neuroendocrine neoplasm of the breast", "breast neuroendocrine tumor, well differentiated, low or intermediate grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast neuroendocrine neoplasm", "shortest_name_length": 10}
{"curie": "MONDO:0011573", "names": ["PSORS7", "psoriasis 7", "psoriasis susceptibility 7", "psoriasis, protection against", "PSORIASIS 7, SUSCEPTIBILITY TO", "psoriasis 7, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "psoriasis 7, susceptibility to", "shortest_name_length": 6}
{"curie": "MONDO:0007549", "names": ["EBDD", "DDEB", "EBDSC", "EBDCT", "DDEB-gen", "DDEB, generalized", "Cockayne-Touraine Disease", "Cockayne Touraine Disease", "Hyperplastic epidermolysis bullosa", "Albopapuloid dominant dystrophic EB", "epidermolysis bullosa dystrophica, AD", "Cockayne Touraine epidermolysis bullos", "Cockayne Touraine epidermolysis bullosa", "Dermolytic bullous dermatosis, dominant", "DDEB, Pasini and Cockayne-Touraine types", "Dominant dystrophic epidermolysis bullosa", "dominant dystrophic epidermolysis bullosa", "Epidermolysis bullosa dystrophica dominans", "Epidermolysis Bullosa Dystrophica, Dominant", "Epidermolysis bullosa dystrophica, dominant", "Cockayne-Touraine Type Epidermolysis Bullosa", "Cockayne Touraine Type Epidermolysis Bullosa", "Epidermolysis bullosa, Cockayne-Touraine type", "Hyperplastic dystrophic epidermolysis bullosa", "Epidermolysis bullosa dystrophica, Pasini type", "epidermolysis bullosa dystrophica, Pasini type", "EPIDERMOLYSIS BULLOSA DYSTROPHICA, PASINI TYPE", "Epidermolysis bullosa dystrophica, Parsini type", "DDEB (dominant dystrophic epidermolysis bullosa)", "Dominant dystrophic epidermolysis bullosa of Pasini", "autosomal dominant dystrophic epidermolysis bullosa", "Dystrophic Epidermolysis Bullosa, Autosomal Dominant", "dystrophic epidermolysis bullosa, autosomal dominant", "Dominant dystrophic epidermolysis bullosa (disorder)", "DYSTROPHIC EPIDERMOLYSIS BULLOSA, AUTOSOMAL DOMINANT", "generalized dominant dystrophic epidermolysis bullosa", "Epidermolysis Bullosa Dystrophica, Autosomal Dominant", "epidermolysis bullosa dystrophica, autosomal dominant", "EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL DOMINANT", "ALBOPAPULOID DOMINANT DYSTROPHIC EPIDERMOLYSIS BULLOSA", "Albopapuloid dominant dystrophic epidermolysis bullosa", "dominant dystrophic epidermolysis bullosa, generalized", "Albopapuloid dystrophic epidermolysis bullosa of Pasini", "Epidermolysis Bullosa Dystrophica, Cockayne Touraine Type", "epidermolysis bullosa dystrophica, Pasini type (formerly)", "Epidermolysis Bullosa Dystrophica, Cockayne-Touraine Type", "EPIDERMOLYSIS BULLOSA DYSTROPHICA, COCKAYNE-TOURAINE TYPE", "epidermolysis bullosa dystrophica, Cockayne-Touraine type", "Epidermolysis Bullosa Dystrophica With Subcorneal Cleavage", "epidermolysis bullosa dystrophica with subcorneal cleavage", "EPIDERMOLYSIS BULLOSA DYSTROPHICA WITH SUBCORNEAL CLEAVAGE", "Dominant dystrophic epidermolysis bullosa, albopapular type", "epidermolysis bullosa dystrophica, Cockayne-Touraine type (formerly)", "Dominant dystrophic epidermolysis bullosa, albopapular type (disorder)", "autosomal dominant dystrophic epidermolysis bullosa, Pasini and Cockayne-Touraine types"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "generalized dominant dystrophic epidermolysis bullosa", "shortest_name_length": 4}
{"curie": "MONDO:0009576", "names": ["MGC1", "MGCN", "macrocornea", "Macrocornea", "Megalocornea", "megalocornea", "MEGALOCORNEA", "keratoglobus", "Keratoglobus", "Cornea enlarged", "Cornea globular", "Enlarged cornea", "MGCN - Megalocornea", "Congenital macrocornea", "megalocornea (disease)", "Congenital megalocornea", "Congenital keratoglobus", "Megalocornea (disorder)", "anterior megalophthalmos", "Anterior megalophthalmos", "keratoglobus; congenital", "congenital; keratoglobus", "Increased corneal diameter", "Corneal diameter increased", "Congenital keratoglobus (disorder)", "congenital anterior megalophthalmia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "megalocornea", "shortest_name_length": 4}
{"curie": "UMLS:C1335723", "names": ["Refractory Follicular Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Follicular Lymphoma", "shortest_name_length": 30}
{"curie": "UMLS:C1335717", "names": ["Recurrent Non-Cutaneous Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Non-Cutaneous Melanoma", "shortest_name_length": 32}
{"curie": "UMLS:C5555952", "names": ["Uterine Ligament Wolffian Tumor", "Wolffian Tumor of the Uterine Ligament"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Ligament Wolffian Tumor", "shortest_name_length": 31}
{"curie": "MONDO:0007637", "names": ["FECD1", "Fuchs' dystrophy", "Dystrophia epithelialis corneae", "COL8A2 Fuchs' endothelial dystrophy", "corneal dystrophy, Fuchs endothelial, 1", "CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 1", "Corneal Dystrophy, Fuchs Endothelial, 1", "Corneal dystrophy, Fuchs' endothelial, 1", "corneal dystrophy, Fuchs endothelial, type 1", "FECD1 Fuchs' endothelial corneal dystrophy 1", "Corneal Dystrophy, Fuchs Endothelial, Early-Onset", "CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, EARLY-ONSET", "Fuchs' endothelial corneal dystrophy, early-onset", "corneal dystrophy, Fuchs endothelial, early-onset", "Corneal dystrophy, Fuchs' endothelial, early-onset", "Fuchs' endothelial dystrophy caused by mutation in COL8A2", "Early-onset FECD Early-onset Fuchs' endothelial corneal dystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal dystrophy, Fuchs endothelial, 1", "shortest_name_length": 5}
{"curie": "MONDO:0009353", "names": ["MTHFR", "MTHFR deficiency", "MTHFR DEFICIENCY", "MTHFR DEFICIENCY, THERMOLABILE TYPE", "MTHFR deficiency, thermolabile type", "Mthfr Deficiency, Thermolabile Type", "homocystinuria due to MTHFR deficiency", "METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY", "methylenetetrahydrofolate reductase deficiency", "Methylenetetrahydrofolate reductase deficiency", "methylene tetrahydrofolate reductase deficiency", "Methylene tetrahydrofolate reductase deficiency", "Methylenetetrahydro-folate reductase deficiency", "5,10-Methylenetetrahydrofolate reductase deficiency", "5,10-Methylenetetrahydrofolate Reductase Deficiency", "5' 10' Methylenetetrahydrofolate Reductase Deficiency", "methylenetetrahydrofolate reductase deficiency (diagnosis)", "5,10-alpha-methylenetetrahydro-folate reductase deficiency", "5,10 alpha methylenetetrahydro-folate reductase deficiency", "5' 10' Methylenetetrahydrofolate Reductase Deficiency (MTHFR)", "5,10-Methylenetetrahydrofolate reductase deficiency (disorder)", "Homocystinuria due to methylene tetrahydrofolate reductase deficiency", "homocystinuria due to methylene tetrahydrofolate reductase deficiency", "Homocysteinuria due to methylenetetrahydro-folate reductase deficiency", "Homocysteinemia due to methylenetetrahydro-folate reductase deficiency", "HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATE REDUCTASE ACTIVITY", "homocystinuria due to deficiency of N(5,10)-methylenetetrahydrofolate reductase activity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "homocystinuria due to methylene tetrahydrofolate reductase deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C1699695", "names": ["Abdominal soft tissue necrosis", "necrosis soft tissue abdominal", "necrosis of abdominal soft tissue", "Abdominal Soft Tissue Necrotic Lesion", "necrosis of abdominal soft tissue (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abdominal Soft Tissue Necrotic Lesion", "shortest_name_length": 30}
{"curie": "MONDO:0013270", "names": ["FOXG1 syndrome", "FOXG1 syndrome (disorder)", "FOXG1 syndrome (diagnosis)", "Rett Syndrome, Congenital Variant", "RETT SYNDROME, CONGENITAL VARIANT", "Rett syndrome, congenital variant", "pervasive developmental disorders FOXG1 syndrome", "FOXG1-related epileptic-dyskinetic encephalopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rett syndrome, congenital variant", "shortest_name_length": 14}
{"curie": "MONDO:0002533", "names": ["Papillary Adenoma", "papillary adenoma", "Papillary adenoma", "Papillary Adenomas", "Adenoma, Papillary", "Adenomas, Papillary", "Glandular Papilloma", "glandular papilloma", "Glandular papilloma", "Papillary adenoma NOS", "Papillary adenoma, NOS", "adenoma, papillary, benign", "ADENOMA, PAPILLARY, BENIGN", "Papillary adenoma (morphologic abnormality)", "papillary adenoma NOS (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papillary adenoma", "shortest_name_length": 17}
{"curie": "MONDO:0010190", "names": ["Pch2", "PCH2", "PCH2A", "Volendam neurodegenerative disease", "VOLENDAM NEURODEGENERATIVE DISEASE", "pontocerebellar hypoplasia type 2A", "Pontocerebellar Hypoplasia Type 2A", "Volendam Neurodegenerative Disease", "pontocerebellar hypoplasia, type 2A", "PONTOCEREBELLAR HYPOPLASIA, TYPE 2A", "TSEN54 pontocerebellar hypoplasia type 2", "microcephaly pontocerebellar hypoplasia dyskinesia", "PONTOCEREBELLAR HYPOPLASIA WITH PROGRESSIVE CEREBRAL ATROPHY", "pontocerebellar hypoplasia with progressive cerebral atrophy", "Pontocerebellar Hypoplasia with Progressive Cerebral Atrophy", "pontocerebellar hypoplasia type 2 caused by mutation in TSEN54"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pontocerebellar hypoplasia type 2A", "shortest_name_length": 4}
{"curie": "UMLS:C2609093", "names": ["Metastatic Pancreatic Islet Cell Tumor", "Pancreatic neuroendocrine tumor metastatic", "Metastatic Pancreatic Neuroendocrine Tumor", "Pancreatic neuroendocrine tumour metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic neuroendocrine tumor metastatic", "shortest_name_length": 38}
{"curie": "MONDO:0009665", "names": ["BTD Deficiency", "BTD deficiency", "BTD DEFICIENCY", "Deficiency, BTD", "BTD Deficiencies", "Deficiencies, BTD", "biotin deficiency", "Biotinidase deficiency", "biotinidase deficiency", "BIOTINIDASE DEFICIENCY", "Biotinidase Deficiency", "Deficiency, Biotinidase", "Biotinidase Deficiencies", "Deficiencies, Biotinidase", "Deficiency of biotinidase", "deficiency of biotinidase", "Biotinidase deficiency (disorder)", "biotinidase deficiency (diagnosis)", "Juvenile multiple carboxylase deficiency", "late-onset multiple carboxylase deficiency", "Late Onset Multiple Carboxylase Deficiency", "Late-onset multiple carboxylase deficiency", "Late-Onset Multiple Carboxylase Deficiency", "multiple carboxylase deficiency, late-onset", "Multiple Carboxylase Deficiency, Late-Onset", "Multiple Carboxylase Deficiency, Late Onset", "MULTIPLE CARBOXYLASE DEFICIENCY, LATE-ONSET", "Carboxylase Deficiency, Multiple, Late-Onset", "Multiple carboxylase deficiency - late onset", "Deficiency, Multiple Carboxylase, Late-Onset", "Juvenile-onset multiple carboxylase deficiency", "juvenile-onset multiple carboxylase deficiency", "MULTIPLE CARBOXYLASE DEFICIENCY, JUVENILE-ONSET", "multiple carboxylase deficiency, juvenile-onset", "Multiple Carboxylase Deficiency, Juvenile-Onset", "Late Onset Biotin Responsive Multiple Carboxylase Deficiency", "Late-Onset Biotin-Responsive Multiple Carboxylase Deficiency", "late-onset biotin-responsive multiple carboxylase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "biotinidase deficiency", "shortest_name_length": 14}
{"curie": "UMLS:C0347004", "names": ["Metastasis to epididymis", "Metastatic tumor to epididymis", "Metastatic tumour to epididymis", "Metastatic Tumor to the Epididymis", "Metastatic Neoplasm to the Epididymis", "epididymis neoplasm malignant secondary", "Secondary malignant neoplasm of epididymis", "Metastatic malignant neoplasm to epididymis", "Metastatic malignant neoplasm of epididymis", "Metastatic Malignant Neoplasm to the Epididymis", "Metastatic Malignant Neoplasm in the Epididymis", "Secondary malignant neoplasm of epididymis (diagnosis)", "Metastatic malignant neoplasm to epididymis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to epididymis", "shortest_name_length": 24}
{"curie": "UMLS:C3179194", "names": ["GALNS Deficiency", "Deficiency, GALNS", "GALNS Deficiencies", "Deficiencies, GALNS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "GALNS Deficiency", "shortest_name_length": 16}
{"curie": "MONDO:0013181", "names": ["AI2A3", "Ai2a3", "WDR72 amelogenesis imperfecta", "amelogenesis imperfecta type IIA3", "amelogenesis imperfecta, type IIA3", "amelogenesis imperfecta hypomaturation type 2A3", "amelogenesis imperfecta hypomaturation type IIA3", "Amelogenesis Imperfecta, Hypomaturation Type, Iia3", "amelogenesis imperfecta, hypomaturation type, IIA3", "AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA3", "amelogenesis imperfecta caused by mutation in WDR72"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amelogenesis imperfecta hypomaturation type 2A3", "shortest_name_length": 5}
{"curie": "MONDO:0014735", "names": ["CMT2Y", "CMT2 due to VCP mutation", "Charcot-Marie-Tooth Disease Type 2Y", "Charcot-Marie-Tooth disease type 2Y", "CHARCOT-MARIE-TOOTH DISEASE, TYPE 2Y", "Charcot-Marie-Tooth disease, type 2Y", "Charcot-Marie-Tooth neuropathy type 2Y", "VCP Charcot-Marie-Tooth disease type 2", "Charcot-Marie-Tooth neuropathy, type 2Y", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2Y", "Charcot-Marie-Tooth disease, axonal, type 2Y", "Charcot-Marie-Tooth disease, axonal, type 2y", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Y", "autosomal dominant axonal Charcot-Marie-Tooth type 2Y", "autosomal dominant Charcot-Marie-Tooth disease type 2Y", "Autosomal dominant Charcot-Marie-Tooth disease type 2Y", "Charcot-Marie-Tooth disease type 2 caused by mutation in VCP", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2Y", "Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2Y", "Autosomal dominant Charcot-Marie-Tooth disease type 2Y (disorder)", "autosomal dominant Charcot-Marie-Tooth disease type 2Y (diagnosis)", "Autosomal dominant Charcot-Marie-Tooth disease type 2 due to VCP mutation", "autosomal dominant Charcot-Marie-Tooth disease type 2 due to VCP mutation", "Autosomal dominant Charcot-Marie-Tooth disease type 2 due to VCP (valosin containing protein) mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 2Y", "shortest_name_length": 5}
{"curie": "MONDO:0002166", "names": ["rectal lymphoma", "rectum lymphoma", "Rectal Lymphoma", "Lymphoma of Rectum", "Lymphoma of rectum", "lymphoma of rectum", "lymphoma of the rectum", "Lymphoma of the Rectum", "Primary Rectal Lymphoma", "primary rectal lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rectum lymphoma", "shortest_name_length": 15}
{"curie": "MONDO:0015362", "names": ["autosomal dominant dHMN", "autosomal dominant distal spinal muscular atrophy", "autosomal dominant distal hereditary motor neuropathy", "distal hereditary motor neuropathy, autosomal dominant", "autosomal dominant distal hereditary motor neuronopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant distal hereditary motor neuropathy", "shortest_name_length": 23}
{"curie": "UMLS:C4687703", "names": ["Pericardial Teratoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pericardial Teratoma", "shortest_name_length": 20}
{"curie": "UMLS:C0936261", "names": ["Brain Thrombus", "Thrombus, Brain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brain Thrombus", "shortest_name_length": 14}
{"curie": "UMLS:C4331901", "names": ["Idiopathic 46,XY Disorder of Sex Development", "Idiopathic 46,XY Differences of Sex Development"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Idiopathic 46,XY Differences of Sex Development", "shortest_name_length": 44}
{"curie": "MONDO:0009523", "names": ["Lichtenstein syndrome", "LICHTENSTEIN SYNDROME", "Lichtenstein syndrome (disorder)", "Lichtenstein syndrome (diagnosis)", "immunodeficiency disease congenital lichtenstein syndrome", "neutropenia immunoglobulin deficiency peculiar facies and bony anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lichtenstein syndrome", "shortest_name_length": 21}
{"curie": "UMLS:C0751761", "names": ["Upper Airway Resistance Sleep Apnea Syndrome", "Syndrome, Upper Airway Resistance, Sleep Apnea"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Upper Airway Resistance Sleep Apnea Syndrome", "shortest_name_length": 44}
{"curie": "UMLS:C1868752", "names": ["Procedural nausea"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Procedural nausea", "shortest_name_length": 17}
{"curie": "MONDO:0013100", "names": ["ATFB8", "ATRIAL FIBRILLATION, FAMILIAL, 8", "Atrial Fibrillation, Familial, 8", "atrial fibrillation, familial, 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial fibrillation, familial, 8", "shortest_name_length": 5}
{"curie": "MONDO:0041850", "names": ["Gram negative pneumonia", "gram negative pneumonia", "gram-negative pneumonia", "pneumonia gram negative", "Gram-negative pneumonia NOS", "Gram negative pneumonia (diagnosis)", "Pneumonia gram-negative bacterial NOS", "pneumonia due to gram-negative bacteria", "pneumonia due to gram negative bacteria", "Pneumonia due to Gram negative bacteria", "Pneumonia due to Gram-negative bacteria", "pneumonia caused by gram negative bacteria", "Pneumonia caused by Gram-negative bacteria", "Pneumonia caused by Gram negative bacteria", "pneumonia caused by gram-negative bacteria", "pneumonia due to other gram-negative bacteria", "Pneumonia due to other Gram-negative bacteria", "Pneumonia due to other gram-negative bacteria", "Pneumonia caused by Gram negative bacteria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pneumonia caused by gram negative bacteria", "shortest_name_length": 23}
{"curie": "MONDO:0016092", "names": ["serous cystadenoma of ovary in childhood", "mucinous cystadenoma of ovary in childhood", "serous or mucinous cystadenoma of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "serous or mucinous cystadenoma of childhood", "shortest_name_length": 40}
{"curie": "UMLS:C0276074", "names": ["Pseudomonal arthritis", "Arthritis due to Pseudomonas", "Arthritis caused by Pseudomonas", "Pseudomonas arthritis or polyarthritis", "Arthritis caused by Pseudomonas (disorder)", "Arthritis or polyarthritis due to Pseudomonas", "Arthritis or Polyarthritis due to Pseudomonas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arthritis due to Pseudomonas", "shortest_name_length": 21}
{"curie": "MONDO:0024553", "names": ["MLASA", "MLASA1", "MITOCHONDRIAL MYOPATHY AND SIDEROBLASTIC ANEMIA", "Mitochondrial myopathy and sideroblastic anemia", "mitochondrial myopathy and sideroblastic anemia", "Myopathy, lactic acidosis and sideroblastic anemia", "Myopathy, lactic acidosis and sideroblastic anaemia", "MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 1", "myopathy, lactic acidosis, and sideroblastic anemia 1", "Myopathy with lactic acidosis and sideroblastic anemia", "PUS1 myopathy, lactic acidosis, and sideroblastic anemia", "Mitochondrial myopathy with sideroblastic anemia syndrome", "Mitochondrial myopathy with sideroblastic anaemia syndrome", "Mitochondrial myopathy with sideroblastic anemia syndrome (disorder)", "myopathy, lactic acidosis, and sideroblastic anemia caused by mutation in PUS1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy, lactic acidosis, and sideroblastic anemia 1", "shortest_name_length": 5}
{"curie": "MONDO:0004134", "names": ["Dermal Schwannoma", "Cutaneous Schwannoma", "benign skin schwannoma", "Benign Skin Schwannoma", "Benign Skin Neurilemmoma", "Benign Dermal Schwannoma", "benign skin neurilemmoma", "benign dermal schwannoma", "Benign Schwannoma of Skin", "benign schwannoma of skin", "Benign Dermal Neurilemmoma", "benign dermal neurilemmoma", "benign neurilemmoma of skin", "Benign Neurilemmoma of Skin", "benign Schwannoma of the skin", "benign schwannoma of the skin", "Benign Schwannoma of the Skin", "benign neurilemmoma of the skin", "Benign Neurilemmoma of the Skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign dermal neurilemmoma", "shortest_name_length": 17}
{"curie": "MONDO:0019136", "names": ["zygomycosis", "Zygomycoses", "Zygomycetes", "ZYGOMYCOSIS", "zygomycoses", "Mucormycose", "Zygomycosis", "Phycomycoses", "Phycomycosis", "mucormycoses", "mucormycosis", "PHYCOMYCOSIS", "Mucormycosis", "MUCORMYCOSIS", "Mucormycoses", "phycomycosis", "Zygomycosis NOS", "Phycomycosis NOS", "Mucorales Infection", "Infection, Mucorales", "Mucorales Infections", "Zygomycosis (disorder)", "Mucormycosis (disorder)", "mucormycosis (diagnosis)", "Zygomycosis, unspecified", "phycomycosis (diagnosis)", "disseminated mucormycosis", "Mucormycosis, unspecified", "Phycomycosis or Mucormycosis", "Zygomycota infectious disease", "Zygomycosis [Phycomycosis or Mucormycosis]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Zygomycosis", "shortest_name_length": 11}
{"curie": "MONDO:0030875", "names": ["FTDALS5", "frontotemporal dementia and/or amyotrophic lateral sclerosis 5", "FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontotemporal dementia and/or amyotrophic lateral sclerosis 5", "shortest_name_length": 7}
{"curie": "UMLS:C4528621", "names": ["Stage IIIA Vulvar Cancer", "Stage IIIA Vulvar Cancer AJCC v8", "Stage IIIA Vulvar Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Vulvar Cancer AJCC v8", "shortest_name_length": 24}
{"curie": "MONDO:0019612", "names": ["Gonadotropinoma", "Gonadotrophinoma", "Gonadotrope Adenoma", "gonadotroph adenoma", "Gonadotroph adenoma", "Gonadotroph Cell Adenoma", "Gonadotroph PitNET/Adenoma", "pituitary adenoma gonadotroph", "Gonadotroph pituitary adenoma", "Gonadotroph adenoma (disorder)", "Gonadotropin-Producing Adenoma", "Gonadotroph adenoma (diagnosis)", "Functioning gonadotropic adenoma", "functioning gonadotropic adenoma", "Gonadotrophin-secreting pituitary adenoma", "functioning pituitary gonadotropic adenoma", "Functioning pituitary gonadotropic adenoma", "Gonadotroph Pituitary Neuroendocrine Tumor", "functioning eosinophilic pituitary adenoma", "Gonadotropin-Producing Pituitary Gland Adenoma", "Gonadotropin-Secreting Pituitary Gland Adenoma", "Gonadotropin Producing Pituitary Gland Adenoma", "Gonadotroph Pituitary Neuroendocrine Tumor/Adenoma", "Gonadotroph pituitary adenoma (morphologic abnormality)", "pituitary growth hormone producing (eosinophilic) adenoma", "pituitary growth hormone producing (eosinophilic) adenoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "functioning gonadotropic adenoma", "shortest_name_length": 15}
{"curie": "UMLS:C4683745", "names": ["Stage III Mycosis Fungoides and Sezary Syndrome AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Mycosis Fungoides and Sezary Syndrome AJCC v8", "shortest_name_length": 55}
{"curie": "UMLS:C4055452", "names": ["Antimicrobial - Induced Nephropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Antimicrobial - Induced Nephropathy", "shortest_name_length": 35}
{"curie": "MONDO:0044789", "names": ["digital papillary carcinoma", "Digital Papillary Carcinoma", "Digital papillary adenocarcinoma", "Digital Papillary Adenocarcinoma", "digit papillary eccrine carcinoma", "digital papillary carcinoma of skin", "digital papillary eccrine carcinoma", "Digital Papillary Eccrine Carcinoma", "Papillary Digital Eccrine Carcinoma", "papillary digital eccrine carcinoma", "papillary eccrine carcinoma of digit", "Aggressive Digital Papillary Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "digital papillary eccrine carcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0019578", "names": ["nodular lichen myxedematosus", "Nodular lichen myxedematosus", "Nodular lichen myxoedematosus", "Nodular lichen myxedematosus (disorder)", "Atypical tuberous myxedema of Jadassohn-Dosseker", "atypical tuberous myxedema of Jadassohn-Dosseker", "Atypical tuberous myxedema of Jadassohn Dosseker", "Atypical tuberous myxoedema of Jadassohn Dosseker"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nodular lichen myxedematosus", "shortest_name_length": 28}
{"curie": "MONDO:0010539", "names": ["MFD Toriello type", "Branchial arch syndrome X-linked", "X-linked branchial arch syndrome", "branchial arch syndrome X-linked", "BRANCHIAL ARCH SYNDROME, X-LINKED", "branchial arch syndrome, X-linked", "Branchial Arch Syndrome, X-Linked", "X-linked mandibulofacial dysostosis", "mandibulofacial dysostosis, X-linked", "Mandibulofacial dysostosis Toriello type", "mandibulofacial dysostosis Toriello type", "MANDIBULOFACIAL DYSOSTOSIS, TORIELLO TYPE", "mandibulofacial dysostosis, Toriello type", "Mandibulofacial Dysostosis, Toriello Type", "Mandibulofacial dysostosis, Toriello type", "X-linked mandibulofacial dysostosis (disorder)", "X-linked mandibulofacial dysostosis with limb anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked mandibulofacial dysostosis", "shortest_name_length": 17}
{"curie": "MONDO:0007375", "names": ["EBMD", "Cogan-Guerry syndrome", "COGAN CORNEAL DYSTROPHY", "Cogan corneal dystrophy", "Cogan's corneal dystrophy", "corneal dystrophy epithelial", "Epithelial corneal dystrophy", "Map-dot-fingerprint dystrophy", "Dystrophy, epithelial corneal", "microcystic corneal dystrophy", "Corneal dystrophy, Cogan type", "Map dot fingerprint dystrophy", "Corneal Dystrophy, Microcystic", "epithelial dystrophy of cornea", "CORNEAL DYSTROPHY, MICROCYSTIC", "corneal dystrophy, microcystic", "Anterior membrane corneal dystrophy", "Microcystic dystrophy of the cornea", "microcystic dystrophy of the cornea", "Basement membrane corneal dystrophy", "MDF - Map dot fingerprint dystrophy", "Anterior basement membrane dystrophy", "anterior basement membrane dystrophy", "Microscopic cystic corneal dystrophy", "Epithelial stromal corneal dystrophy", "Corneal dystrophy, microscopic cystic", "Map-dot-fingerprint corneal dystrophy", "Microcystic corneal dystrophy syndrome", "Epithelial basement membrane dystrophy", "epithelial basement membrane dystrophy", "Cogan's epithelial dystrophy of cornea", "Cogan microcystic epithelial dystrophy", "Map-dot-fingerprint dystrophy of cornea", "Epithelial corneal dystrophy (diagnosis)", "Corneal Dystrophy, Map-Dot-Fingerprint Type", "CORNEAL DYSTROPHY, MAP-DOT-FINGERPRINT TYPE", "corneal dystrophy, Map-Dot-Fingerprint type", "CORNEAL DYSTROPHY, ANTERIOR BASEMENT MEMBRANE", "corneal dystrophy, anterior basement Membrane", "Corneal dystrophy, anterior basement membrane", "EBMD - Epithelial basement membrane dystrophy", "epithelial basement membrane corneal dystrophy", "corneal dystrophy, epithelial basement MEMBRANE", "Corneal dystrophy, epithelial basement membrane", "CORNEAL DYSTROPHY, EPITHELIAL BASEMENT MEMBRANE", "epithelial dystrophy of cornea (physical finding)", "Epithelial basement membrane dystrophy (disorder)", "Corneal epithelial and basement membrane dystrophy", "Cogan's epithelial dystrophy of cornea (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epithelial basement membrane dystrophy", "shortest_name_length": 4}
{"curie": "UMLS:C4727166", "names": ["Metastatic Unresectable Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Unresectable Carcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C1328552", "names": ["Extrapulmonary pneumocystosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extrapulmonary pneumocystosis", "shortest_name_length": 29}
{"curie": "MONDO:0008330", "names": ["PSEUDOMONILETHRIX", "Pseudomonilethrix", "pseudomonilethrix", "Pseudomonilethrix (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudomonilethrix", "shortest_name_length": 17}
{"curie": "MONDO:0008026", "names": ["SMALED", "Sma-led", "SMALED1", "Kugelberg-Welander syndrome, autosomal dominant", "Kugelberg-Welander Syndrome, Autosomal Dominant", "KUGELBERG-WELANDER SYNDROME, AUTOSOMAL DOMINANT", "Spinal muscular atrophy with lower extremity predominance", "spinal muscular atrophy with lower extremity predominant 1", "spinal muscular atrophy, lower extremity-predominant 1, AD", "spinal muscular atrophy with lower extremity predominance 1", "SMALED - spinal muscular atrophy, lower extremity, dominant", "Spinal Muscular Atrophy, Juvenile, Proximal, Autosomal Dominant", "spinal muscular atrophy, juvenile, proximal, autosomal dominant", "SPINAL MUSCULAR ATROPHY, JUVENILE, PROXIMAL, AUTOSOMAL DOMINANT", "SPINAL MUSCULAR ATROPHY, CHILDHOOD, PROXIMAL, AUTOSOMAL DOMINANT", "spinal muscular atrophy, childhood, proximal, autosomal dominant", "Spinal Muscular Atrophy, Childhood, Proximal, Autosomal Dominant", "Autosomal dominant childhood-onset proximal spinal muscular atrophy", "spinal muscular atrophy, LOWER extremity-predominant, 1, autosomal dominant", "SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 1, AUTOSOMAL DOMINANT", "Autosomal dominant childhood-onset proximal spinal muscular atrophy (disorder)", "Lower extremity-predominant autosomal dominant proximal spinal muscular atrophy", "DYNC1H1-related autosomal dominant childhood-onset proximal spinal muscular atrophy", "autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures", "DYNC1H1-related lower extremity-predominant autosomal dominant proximal spinal muscular atrophy", "Lower extremity-predominant autosomal dominant proximal spinal muscular atrophy without contractures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures", "shortest_name_length": 6}
{"curie": "UMLS:C1335482", "names": ["Gastric Burkitt Lymphoma", "Gastric Burkitt's Lymphoma", "Primary Gastric Burkitt's Lymphoma", "Primary Burkitt's Lymphoma of Stomach", "Primary Burkitt's Lymphoma of the Stomach"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Burkitt Lymphoma", "shortest_name_length": 24}
{"curie": "UMLS:C0280193", "names": ["Grade Adult NonHodgkins Lymphoma", "Adult NonHodgkins Lymphoma Grade", "Grade Adult NonHodgkin's Lymphoma", "Adult NonHodgkin's Lymphoma Grade", "Grade Adult Non-Hodgkins Lymphoma", "Adult Non-Hodgkins Lymphoma Grade", "adult non-Hodgkin's lymphoma grade", "Adult Non-Hodgkin's Lymphoma Grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Non-Hodgkin's Lymphoma Grade", "shortest_name_length": 32}
{"curie": "MONDO:0009992", "names": ["rhabdomyolysis, acute recurrent", "Rhabdomyolysis, Acute Recurrent", "RHABDOMYOLYSIS, ACUTE RECURRENT", "Myoglobinuria, Familial Paroxysmal Paralytic", "MYOGLOBINURIA, FAMILIAL PAROXYSMAL PARALYTIC", "myoglobinuria, familial paroxysmal paralytic", "myoglobinuria, acute recurrent, autosomal recessive", "MYOGLOBINURIA, ACUTE RECURRENT, AUTOSOMAL RECESSIVE", "Myoglobinuria, Acute Recurrent, Autosomal Recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myoglobinuria, acute recurrent, autosomal recessive", "shortest_name_length": 31}
{"curie": "UMLS:C5239111", "names": ["Metastatic HER2 Negative Breast Carcinoma", "Metastatic HER2-Negative Breast Carcinoma", "Metastatic HER2 Negative Breast Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic HER2-Negative Breast Carcinoma", "shortest_name_length": 41}
{"curie": "UMLS:C0686601", "names": ["Erythroleukemia in remission", "erythroleukemia in remission", "Erythroleukemia in Remission", "Erythroleukaemia in remission", "erythroleukemia in remission (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythroleukemia in remission", "shortest_name_length": 28}
{"curie": "UMLS:C0752292", "names": ["Nocturnal Eating-Drinking Syndrome", "Nocturnal Eating Drinking Syndrome", "Nocturnal Eating-Drinking Syndromes", "Syndrome, Nocturnal Eating-Drinking", "Eating-Drinking Syndrome, Nocturnal", "Nocturnal eating (drinking) syndrome", "Eating-Drinking Syndromes, Nocturnal", "Syndromes, Nocturnal Eating-Drinking"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nocturnal Eating-Drinking Syndrome", "shortest_name_length": 34}
{"curie": "MONDO:0017455", "names": ["Hyperphalangy", "hyperphalangy", "Supernumerary phalanx", "supernumerary phalanx", "Supernumerary phalanges", "supernumerary phalanges", "Supernumerary phalanx (disorder)", "polydactyly supernumerary phalanx", "Supernumerary phalanx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperphalangy", "shortest_name_length": 13}
{"curie": "EFO:1002005", "names": ["lumbar disc herniation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lumbar disc herniation", "shortest_name_length": 22}
{"curie": "UMLS:C1334010", "names": ["High grade cervical glandular intraepithelial neoplasia", "High Grade Cervical Glandular Intraepithelial Neoplasia", "H-CGIN - high grade cervical glandular intraepithelial neoplasia", "High grade cervical glandular intraepithelial neoplasia (disorder)", "High grade cervical glandular intraepithelial neoplasia (diagnosis)", "cervical squamous cell intraepithelial glandular neoplasia high grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High grade cervical glandular intraepithelial neoplasia", "shortest_name_length": 55}
{"curie": "MONDO:0009681", "names": ["UCMD1", "Ullrich disease", "muscular dystrophy, Scleroatonic", "Ullrich congenital muscular dystrophy", "Ullrich congenital muscular dystrophy 1", "Ullrich Scleroatonic muscular dystrophy", "Ullrich congenital muscular dystrophy type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ullrich congenital muscular dystrophy 1", "shortest_name_length": 5}
{"curie": "MONDO:0002422", "names": ["adamantinoma", "Adamantinoma", "Adamantinomas", "long bone adamantinoma", "ADAMANTINOMA, MALIGNANT", "adamantinoma, malignant", "Adamantinoma, malignant", "Long Bones Adamantinoma", "long bones; adamantinoma", "Long Bones Adamantinomas", "adamantinoma; long bones", "Adamantinoma of long bone", "ameloblastoma; long bones", "adamantinoma of long bone", "Extragnathic adamantinoma", "long bones; ameloblastoma", "Extragnathic Adamantinoma", "ADAMANTINOMA OF LONG BONES", "adamantinoma of long bones", "Adamantinoma of long bones", "Adamantinoma of Long Bones", "[M]Adamantinoma of long bones", "malignant adamantinoma of long bone", "Adamantinoma of long bone (disorder)", "[OBSOLETE] Adamantinoma Of Long Bones", "malignant adamantinoma of long bone (diagnosis)", "bone neoplasm malignant adamantinoma of long bone", "adamantinoma of long bones (morphologic abnormality)", "Adamantinoma of long bones (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adamantinoma", "shortest_name_length": 12}
{"curie": "UMLS:C0334564", "names": ["Odontogenic fibrosarcoma", "Ameloblastic odontosarcoma", "odontosarcoma; ameloblastic", "Ameloblastic dentinosarcoma", "Ameloblastic Fibroodontosarcoma", "Ameloblastic fibrodentinosarcoma", "Ameloblastic fibro-odontosarcoma", "Ameloblastic odontosarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ameloblastic Fibroodontosarcoma", "shortest_name_length": 24}
{"curie": "MONDO:0003157", "names": ["Gorham disease", "Gorham's disease", "massive osteolysis", "phantom bone disease", "essential osteolysis", "Essential Osteolysis", "Essential Osteolyses", "Osteolysis, Essential", "Gorham-Stout Syndrome", "Osteolyses, Essential", "Gorham-Stout syndrome", "disappearing bone disease", "Disappearing Bone Disease", "Disappearing bone disease", "Disappearing bone disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disappearing bone disease", "shortest_name_length": 14}
{"curie": "MONDO:0007890", "names": ["LENTIGINOSIS, TOURAINE TYPE", "lentiginosis, Touraine type", "Lentiginosis, Touraine Type", "Lentiginosis, Centrofacial Neurodysraphic", "lentiginosis, centrofacial neurodysraphic", "LENTIGINOSIS, CENTROFACIAL NEURODYSRAPHIC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lentiginosis, centrofacial neurodysraphic", "shortest_name_length": 27}
{"curie": "UMLS:C1302690", "names": ["Retinal thickening", "Retinal thickening (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retinal thickening", "shortest_name_length": 18}
{"curie": "MONDO:0017391", "names": ["GWCD", "Grayson-Wilbrandt corneal dystrophy", "Grayson Wilbrandt corneal dystrophy", "Grayson Wilbrandt dystrophy of cornea", "Grayson Wilbrandt dystrophy of cornea (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grayson-Wilbrandt corneal dystrophy", "shortest_name_length": 4}
{"curie": "UMLS:C3897747", "names": ["Recurrent Oligodendroglioma", "recurrent childhood oligodendroglioma", "Recurrent Childhood Oligodendroglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Oligodendroglioma", "shortest_name_length": 27}
{"curie": "MONDO:0400005", "names": ["refeed syndrome", "Refeeding syndrome", "refeeding syndrome", "Refeeding Syndrome", "Syndrome, Refeeding", "Refeeding syndrome (disorder)", "refeeding syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "refeeding syndrome", "shortest_name_length": 15}
{"curie": "UMLS:C5418265", "names": ["Chronic Respiratory Disease", "Non-Neoplastic Chronic Respiratory System Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Chronic Respiratory System Disorder", "shortest_name_length": 27}
{"curie": "MONDO:0018217", "names": ["Koolen-de Vries syndrome due to a point mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Koolen-de Vries syndrome due to a point mutation", "shortest_name_length": 48}
{"curie": "MONDO:0013611", "names": ["RP62", "RETINITIS PIGMENTOSA 62", "retinitis pigmentosa 62", "MAK retinitis pigmentosa", "retinitis pigmentosa type 62", "retinitis pigmentosa caused by mutation in MAK"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 62", "shortest_name_length": 4}
{"curie": "MONDO:0018491", "names": ["3-phosphoglycerate dehydrogenase deficiency", "3-Phosphoglycerate dehydrogenase deficiency", "3-Phosphoglycerate dehydrogenase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "3-phosphoglycerate dehydrogenase deficiency", "shortest_name_length": 43}
{"curie": "MONDO:0001606", "names": ["CNS Leukemia", "CNS leukemia", "Leukemia of CNS", "leukemia of CNS", "Leukemia of the CNS", "leukemia of the CNS", "CNS leukemia (diagnosis)", "Central nervous system leukemia", "Central Nervous System Leukemia", "central nervous system leukemia", "Central nervous system leukaemia", "leukemia of central nervous system", "Leukemia of Central Nervous System", "leukemia of the central nervous system", "Leukemia of the Central Nervous System", "central nervous system leukemia (disease)", "leukemia (disease) of central nervous system", "leukemia lymphocytic acute (ALL) in relapse CNS leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system leukemia", "shortest_name_length": 12}
{"curie": "UMLS:C5204258", "names": ["Renal Ewing Sarcoma", "Kidney Ewing Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kidney Ewing Sarcoma", "shortest_name_length": 19}
{"curie": "MONDO:0004489", "names": ["Fallopian Tube Gestational Choriocarcinoma", "fallopian tube gestational choriocarcinoma", "gestational choriocarcinoma of fallopian tube", "Gestational Choriocarcinoma of Fallopian Tube", "Gestational Choriocarcinoma of the Fallopian Tube", "Gestational Choriocarcinoma of the fallopian tube", "gestational choriocarcinoma of the fallopian tube"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fallopian tube gestational choriocarcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0021129", "names": ["Nanophthalmos", "nanophthalmos", "Small eyeball", "microphthalmos", "Microphthalmia", "MICROPHTHALMOS", "MICROPHTHALMIA", "microphthalmia", "Microphthalmos", "Globe of eye small", "Microphthalmos, NOS", "Simple microphthalmos", "simple microphthalmos", "Abnormally small eyeball", "Decreased size of eyeball", "congenital microphthalmos", "Congenital microphthalmos", "Microphthalmos (disorder)", "eye findings microphthalmia", "Microphthalmos, unspecified", "microphthalmia was observed", "Abnormally small globe of eye", "Decreased size of globe of eye", "simple congenital microphthalmos", "Simple microphthalmos (disorder)", "microphthalmia (physical finding)", "congenital microphthalmos (diagnosis)", "simple congenital microphthalmos (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microphthalmia", "shortest_name_length": 13}
{"curie": "MONDO:0700167", "names": ["canine sebaceous gland epithelioma", "Canine Sebaceous Gland Epithelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canine sebaceous gland epithelioma", "shortest_name_length": 34}
{"curie": "MONDO:0002333", "names": ["spleen abscess", "Spleen abscess", "abscess spleen", "SPLEEN ABSCESS", "SPLEEN, ABSCESS", "Splenic Abscess", "spleen; abscess", "Splenic abscess", "splenic abscess", "abscesses spleen", "Abscess of spleen", "splenic abscess (disease)", "Splenic abscess (disorder)", "splenic abscess (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "splenic abscess", "shortest_name_length": 14}
{"curie": "UMLS:C4054251", "names": ["Pancreaticobiliary Malunion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreaticobiliary Malunion", "shortest_name_length": 27}
{"curie": "MONDO:0019212", "names": ["disseminated superficial actinic porokeratosis", "Disseminated superficial actinic porokeratosis", "Disseminated Superficial Actinic Porokeratosis", "Porokeratosis, Disseminated Superficial Actinic", "Porokeratosis, disseminated superficial actinic type", "disseminated superficial actinic porokeratosis (DSAP)", "DSAP - Disseminated superficial actinic porokeratosis", "Disseminated superficial actinic porokeratosis (DSAP)", "Disseminated superficial actinic porokeratosis (disorder)", "disseminated superficial actinic porokeratosis (DSAP) (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disseminated superficial actinic porokeratosis", "shortest_name_length": 46}
{"curie": "MONDO:0002255", "names": ["cervix; hypertrophy, elongation", "hypertrophy; cervix, elongation", "cervix; elongation, hypertrophic", "elongation; cervix, hypertrophic", "Hypertrophic elongation of cervix", "hypertrophic elongation of cervix", "Hypertrophic elongation of cervix uteri", "Hypertrophic elongation of cervix (disorder)", "hypertrophic elongation of cervix (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophic elongation of cervix", "shortest_name_length": 31}
{"curie": "UMLS:C5239079", "names": ["Advanced Soft Tissue Leiomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Soft Tissue Leiomyosarcoma", "shortest_name_length": 35}
{"curie": "UMLS:C1271448", "names": ["UGH syndrome", "Uveitis-glaucoma-hyphema syndrome", "Uveitis-hyphema-glaucoma syndrome", "uveitis-hyphema-glaucoma syndrome", "Uveitis-glaucoma-hyphaema syndrome", "Uveitis Glaucoma and Hyphema Syndrome", "UGH (Uveitis Glaucoma Hyphema) Syndrome", "Uveitis-hyphema-glaucoma syndrome (disorder)", "uveitis-hyphema-glaucoma syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uveitis-glaucoma-hyphema syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0007052", "names": ["PAP", "FIS", "IFS", "PITA1", "PAGH1", "pituitary adenoma 1", "SOMATOTROPHINOMA, FAMILIAL", "Somatotrophinoma, familial", "Somatotrophinoma, Familial", "pituitary adenoma predisposition", "PITUITARY ADENOMA PREDISPOSITION", "ISOLATED FAMILIAL SOMATOTROPINOMA", "isolated familial somatotropinoma", "Isolated Familial Somatotropinoma", "somatotropinoma, familial isolated", "SOMATOTROPINOMA, FAMILIAL ISOLATED", "Somatotropinoma, Familial Isolated", "pituitary adenoma 1, multiple types", "PITUITARY ADENOMA 1, MULTIPLE TYPES", "pituitary adenoma, familial isolated", "acromegaly due to pituitary adenoma 1", "ACROMEGALY DUE TO PITUITARY ADENOMA 1", "familial isolated pituitary adenoma syndrome", "growth hormone secreting pituitary adenoma 1", "PITUITARY ADENOMA 1, GROWTH HORMONE-SECRETING", "pituitary adenoma, growth hormone-secreting, 1", "pituitary adenoma, growth hormone-secreting, type 1", "pituitary adenoma predisposition, autosomal dominant, somatic mutation", "pituitary adenoma 1, multiple types, autosomal dominant, somatic mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "growth hormone secreting pituitary adenoma 1", "shortest_name_length": 3}
{"curie": "UMLS:C0751588", "names": ["Benign Supratentorial Tumor", "Benign Supratentorial Tumors", "Benign Supratentorial Neoplasm", "Benign Supratentorial Neoplasms", "Supratentorial Neoplasm, Benign", "Neoplasm, Benign Supratentorial", "Supratentorial Neoplasms, Benign", "Neoplasms, Benign Supratentorial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Supratentorial Neoplasms", "shortest_name_length": 27}
{"curie": "UMLS:C0154659", "names": ["Toxic Encephalitis", "Toxic encephalitis", "toxic encephalitis", "ENCEPHALITIS TOXIC", "Encephalitis toxic", "encephalitis; toxic", "Encephalitis, Toxic", "toxic; encephalitis", "Toxic Encephalitides", "Encephalitides, Toxic", "Toxic encephalitis, NOS", "Toxic encephalitis (disorder)", "toxic encephalitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Toxic Encephalitis", "shortest_name_length": 18}
{"curie": "UMLS:C1709775", "names": ["Pure Cutaneous Mastocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pure Cutaneous Mastocytosis", "shortest_name_length": 27}
{"curie": "MONDO:0011822", "names": ["BARTS3", "adult Bartter syndrome", "Bartter disease type 3", "Bartter syndrome type 3", "Bartter syndrome, type 3", "Bartter syndrome classic", "BARTTER SYNDROME, TYPE 3", "Classic Bartter syndrome", "classic Bartter syndrome", "Bartter syndrome type III", "BARTTER SYNDROME, CLASSIC", "Bartter syndrome, classic", "Bartter's syndrome type 3", "Bartter syndrome type 3 (disorder)", "Bartter syndrome type 3 (diagnosis)", "Bartter syndrome, type 3, with hypocalciuria", "Bartter Syndrome, Type 3, with Hypocalciuria", "BARTTER SYNDROME, TYPE 3, WITH HYPOCALCIURIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bartter disease type 3", "shortest_name_length": 6}
{"curie": "UMLS:C5670381", "names": ["COMMON CAROTID TRUNK", "Common Carotid Trunk"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Common Carotid Trunk", "shortest_name_length": 20}
{"curie": "MONDO:0014403", "names": ["GHDP", "ghrelin receptor deficiency", "Ghrelin receptor deficiency", "short stature due to GHSR deficiency", "Short stature due to GHSR deficiency", "growth hormone deficiency, isolated partial", "short stature due to growth hormone secretagogue receptor deficiency", "Short stature due to growth hormone secretagogue receptor deficiency", "Short stature due to GHSR (growth hormone secretagogue receptor) deficiency", "Short stature due to growth hormone secretagogue receptor deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short stature due to GHSR deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0001454", "names": ["Blessig cysts", "iwanoff's cysts", "Iwanoff's cysts", "blessig's cysts", "Blessig's cysts", "Microcystoid degeneration", "microcystoid retinal degeneration", "Microcystoid retinal degeneration", "Microcystoid degeneration of retina", "microcystoid peripheral retinal degeneration", "Microcystoid retinal degeneration (disorder)", "microcystoid retinal degeneration (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Blessig's cysts", "shortest_name_length": 13}
{"curie": "UMLS:C1337020", "names": ["Well Differentiated Prostate Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Well Differentiated Prostate Adenocarcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0100073", "names": ["MRSA", "methicillin-resistant staphylococcus aureus infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "methicillin-resistant staphylococcus aureus infectious disease", "shortest_name_length": 4}
{"curie": "MONDO:0021453", "names": ["benign retina tumor", "Benign Retina Tumor", "Benign retinal tumor", "Benign Retinal Tumor", "benign retinal tumor", "Benign retinal tumour", "benign tumor of retina", "benign retina neoplasm", "Benign tumor of retina", "retina benign neoplasm", "Benign Tumor of Retina", "Benign Retina Neoplasm", "benign retinal neoplasm", "Benign tumour of retina", "Benign Retinal Neoplasm", "Benign neoplasm of retina", "Benign Neoplasm of Retina", "benign neoplasm of retina", "Benign Tumor of the Retina", "benign tumor of the retina", "Benign retinal neoplasm NOS", "benign neoplasm of the retina", "Benign Neoplasm of the Retina", "Benign neoplasm of retina (disorder)", "benign neoplasm of retina (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of retina", "shortest_name_length": 19}
{"curie": "MONDO:0011605", "names": ["GBFHS", "generalized basaloid follicular hamartoma syndrome", "Generalised basaloid follicular hamartoma syndrome", "Generalized basaloid follicular hamartoma syndrome", "Generalized basaloid follicular hamartoma syndrome (disorder)", "basaloid follicular hamartoma syndrome, generalized, autosomal dominant", "BASALOID FOLLICULAR HAMARTOMA SYNDROME, GENERALIZED, AUTOSOMAL DOMINANT", "Basaloid Follicular Hamartoma Syndrome, Generalized, Autosomal Dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "generalized basaloid follicular hamartoma syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0008815", "names": ["Asauria", "ASL deficiency", "ASA deficiency", "ASL Deficiency", "ASL DEFICIENCY", "ASA Deficiency", "Deficiency, ASL", "ASAL deficiency", "Deficiency, ASA", "ASL Deficiencies", "ASA Deficiencies", "Deficiencies, ASA", "Deficiencies, ASL", "Argininosuccinicaciduria", "argininosuccinicaciduria", "Argininosuccinic Acidemia", "Argininosuccinic Aciduria", "argininosuccinic acidemia", "Argininosuccinic aciduria", "Argininosuccinicacidurias", "ARGININOSUCCINIC ACIDURIA", "argininosuccinic aciduria", "ACIDURIA, ARGININOSUCCINIC", "acidemia; argininosuccinic", "Argininosuccinate Acidemia", "arginosuccinase deficiency", "Aciduria, Argininosuccinic", "aciduria; argininosuccinic", "argininosuccinic; aciduria", "Arginosuccinase Deficiency", "argininosuccinate acidemia", "Argininosuccinic Acidurias", "argininosuccinic; acidemia", "Acidurias, Argininosuccinic", "Acidemia, Argininosuccinate", "Argininosuccinate Acidemias", "ARGININOSUCCINASE DEFICIENCY", "Acidemias, Argininosuccinate", "argininosuccinase deficiency", "Argininosuccinase deficiency", "Argininosuccinase Deficiency", "arginino succinase deficiency", "Arginino Succinase Deficiency", "Deficiency, Arginino Succinase", "Arginino Succinase Deficiencies", "Deficiencies, Arginino Succinase", "argininosuccinatelyase deficiency", "Argininosuccinatelyase deficiency", "Argininosuccinate lyase deficiency", "Argininosuccinate Lyase Deficiency", "argininosuccinate lyase deficiency", "ARGININOSUCCINATE LYASE DEFICIENCY", "Deficiency, Argininosuccinate Lyase", "Argininosuccinate Lyase Deficiencies", "Deficiencies, Argininosuccinate Lyase", "deficiency of argininosuccinate lyase", "Deficiency of argininosuccinate lyase", "argininosuccinic aciduria (diagnosis)", "Argininosuccinyl-Coa Lyase Deficiency", "argininosuccinic acid lyase deficiency", "Argininosuccinic acid lyase deficiency", "Argininosuccinic Acid Lyase Deficiency", "ARGININOSUCCINIC ACID LYASE DEFICIENCY", "Urea Cycle Disorder, Arginino Succinase Type", "urea cycle disorder, arginino succinase type", "Argininosuccinate lyase deficiency (disorder)", "Inborn Error of Urea Synthesis, Arginino Succinic Type", "inborn error of urea synthesis, arginino succinic type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "argininosuccinic aciduria", "shortest_name_length": 7}
{"curie": "UMLS:C4521749", "names": ["IVA", "Stage IVA Esophageal Squamous Cell Cancer", "Pathologic Stage IVA Esophageal Squamous Cell Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IVA Esophageal Squamous Cell Carcinoma AJCC v8", "shortest_name_length": 3}
{"curie": "MONDO:0011205", "names": ["MCKAT DEFICIENCY", "Mckat deficiency", "Medium-chain ketoacyl-CoA thiolase deficiency", "medium-chain 3-ketoacyl-coa thiolase deficiency", "Medium Chain 3-Ketoacyl-CoA Thiolase Deficiency", "medium chain 3-ketoacyl-Coa thiolase deficiency", "MEDIUM CHAIN 3-KETOACYL-CoA THIOLASE DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "medium chain 3-ketoacyl-Coa thiolase deficiency", "shortest_name_length": 16}
{"curie": "UMLS:C1336475", "names": ["Paranasal Sinus Cancer Stage I", "Stage I Paranasal Sinus Cancer", "Stage I Paranasal Sinus Carcinoma", "Stage I Accessory Sinus Carcinoma", "Stage I Carcinoma of Accessory Sinus", "Stage I Carcinoma of Paranasal Sinus", "Stage I Paranasal Sinus Cancer AJCC v7", "Stage I Paranasal Sinus Cancer AJCC v6", "Stage I Carcinoma of the Accessory Sinus", "Stage I Carcinoma of the Paranasal Sinus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Paranasal Sinus Cancer", "shortest_name_length": 30}
{"curie": "MONDO:0031007", "names": ["SHILCA", "SHILCA syndrome", "SHILCA SYNDROME", "Spondyloepiphyseal dysplasia-sensorineural hearing loss-intellectual disability-Leber congenital amaurosis syndrome", "SPONDYLOEPIPHYSEAL DYSPLASIA, SENSORINEURAL HEARING LOSS, IMPAIRED INTELLECTUAL DEVELOPMENT, AND LEBER CONGENITAL AMAUROSIS", "spondyloepiphyseal dysplasia, sensorineural hearing loss, impaired intellectual development, and leber congenital amaurosis", "spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepiphyseal dysplasia, sensorineural hearing loss, impaired intellectual development, and leber congenital amaurosis", "shortest_name_length": 6}
{"curie": "MONDO:0001845", "names": ["uterine corpus lipoleiomyoma", "Uterine Corpus Lipoleiomyoma", "Uterine Corpus Lipomatous Leiomyoma", "uterine corpus lipomatous leiomyoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine corpus lipoleiomyoma", "shortest_name_length": 28}
{"curie": "MONDO:0018263", "names": ["fetal carbamazepine syndrome", "Fetal carbamazepine syndrome", "Foetal carbamazepine syndrome", "Fetal carbamazepine syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fetal carbamazepine syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0000315", "names": ["commensal bacterial infectious disease", "opportunistic bacterial infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "commensal bacterial infectious disease", "shortest_name_length": 38}
{"curie": "UMLS:C1881083", "names": ["Hyperocclusion", "Hyperocclusion (disorder)", "Premature tooth contact upon closure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyperocclusion", "shortest_name_length": 14}
{"curie": "MONDO:0100516", "names": ["complex neurodevelopmental disorder with motor features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complex neurodevelopmental disorder with motor features", "shortest_name_length": 55}
{"curie": "UMLS:C1336345", "names": ["Stage IVA Lip Cancer", "Stage IVA Lip Carcinoma", "Stage IVA Carcinoma of Lip", "Stage IVA Lip Cancer AJCC v6", "Stage IVA Lip Cancer AJCC v7", "Stage IVA Carcinoma of the Lip", "Stage IVA Lip Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Lip Cancer AJCC v6 and v7", "shortest_name_length": 20}
{"curie": "UMLS:C4763940", "names": ["Non-ischemic Stroke"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-ischemic Stroke", "shortest_name_length": 19}
{"curie": "MONDO:0004441", "names": ["childhood ovarian embryonal carcinoma", "pediatric ovarian embryonal carcinoma", "Pediatric Ovarian Embryonal Carcinoma", "Childhood Ovarian Embryonal Carcinoma", "Childhood Embryonal Carcinoma of Ovary", "Pediatric Embryonal Carcinoma of Ovary", "childhood embryonal carcinoma of ovary", "pediatric Embryonal carcinoma of Ovary", "pediatric embryonal carcinoma of ovary", "ovarian embryonal carcinoma of childhood", "childhood embryonal carcinoma of the ovary", "Childhood Embryonal Carcinoma of the Ovary", "pediatric embryonal carcinoma of the ovary", "Pediatric Embryonal Carcinoma of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood ovarian embryonal carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0004130", "names": ["anal Basaloid carcinoma", "anus basaloid carcinoma", "anal basaloid carcinoma", "Anal Basaloid Carcinoma", "basaloid carcinoma of anus", "Basaloid Carcinoma of Anus", "Basaloid Carcinoma of the Anus", "basaloid carcinoma of the anus", "anus cancer, basaloid carcinoma", "anal cancer, basaloid carcinoma", "anus basaloid squamous cell carcinoma", "basaloid carcinoma of anus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anus basaloid carcinoma", "shortest_name_length": 23}
{"curie": "MONDO:0005254", "names": ["symptomatic heart failure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "symptomatic heart failure", "shortest_name_length": 25}
{"curie": "MONDO:0013929", "names": ["DFNB98", "autosomal recessive deafness 98", "deafness, autosomal recessive 98", "DEAFNESS, AUTOSOMAL RECESSIVE 98", "deafness, autosomal recessive type 98", "autosomal recessive nonsyndromic deafness 98", "autosomal recessive nonsyndromic hearing loss 98", "TSPEAR autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic deafness type 98", "autosomal recessive nonsyndromic deafness caused by mutation in TSPEAR"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 98", "shortest_name_length": 6}
{"curie": "MONDO:0009690", "names": ["LGM", "CMS10", "CMS1B", "CMS Ib", "Cms Ib", "LGM, FORMERLY", "CMS1B, FORMERLY", "Cms Ib, formerly", "CMS Ib, FORMERLY", "myasthenic myopathy", "Myasthenic myopathy", "myasthenic myopathy, formerly", "MYASTHENIC MYOPATHY, FORMERLY", "Myopathy in myasthenia gravis", "familial limb-girdle myasthenia", "Myasthenia, familial limb-girdle", "Congenital myasthenic syndrome ib", "myasthenia, limb-girdle, familial", "Myasthenia, Limb-Girdle, Familial", "congenital myasthenic syndrome 10", "MYASTHENIC SYNDROME, CONGENITAL, 10", "myasthenic syndrome, congenital, 10", "DOK7 congenital myasthenic syndrome", "congenital myasthenic syndrome type IB", "Congenital Myasthenic Syndrome Type Ib", "congenital myasthenic syndrome type 10", "Myopathy in myasthenia gravis (disorder)", "myasthenic syndrome, congenital, type 10", "MYASTHENIA, LIMB-GIRDLE, FAMILIAL, FORMERLY", "myasthenia, limb-girdle, familial, formerly", "congenital muscular dystrophy merosin-positive", "congenital myasthenic syndrome type IB, formerly", "CONGENITAL MYASTHENIC SYNDROME TYPE Ib, FORMERLY", "congenital myasthenic syndrome caused by mutation in DOK7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myasthenic syndrome 10", "shortest_name_length": 3}
{"curie": "MONDO:0054551", "names": ["ANFH2", "avascular necrosis of femoral head, primary, 2", "AVASCULAR NECROSIS OF FEMORAL HEAD, PRIMARY, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "avascular necrosis of femoral head, primary, 2", "shortest_name_length": 5}
{"curie": "UMLS:C0009568", "names": ["Complication of Transplant", "Transplanted Organ Complication", "Complication of Organ Transplant", "complications of organ transplant", "Complications of transplanted organ", "COMPLICATIONS OF TRANSPLANTED ORGANS", "Complication of transplanted organ, NOS", "complications of organ transplant (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Complication of transplanted organ, NOS", "shortest_name_length": 26}
{"curie": "UMLS:C5420080", "names": ["Sinonasal Olfactory Neuroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Olfactory Neuroblastoma", "shortest_name_length": 33}
{"curie": "MONDO:0032596", "names": ["CMS23", "myasthenic syndrome, congenital, 23, presynaptic", "MYASTHENIC SYNDROME, CONGENITAL, 23, PRESYNAPTIC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myasthenic syndrome, congenital, 23, presynaptic", "shortest_name_length": 5}
{"curie": "MONDO:0030055", "names": ["SORDD", "SORBITOL DEHYDROGENASE DEFICIENCY", "Sorbitol Dehydrogenase Deficiency", "SORBITOL DEHYDROGENASE DEFICIENCY WITH PERIPHERAL NEUROPATHY", "sorbitol dehydrogenase deficiency with peripheral neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sorbitol dehydrogenase deficiency with peripheral neuropathy", "shortest_name_length": 5}
{"curie": "UMLS:C1879591", "names": ["Lung adenocar. w/ bronch. feat.", "Lung adenocarcinoma with bronchioloalveolar features", "Lung Adenocarcinoma with Mixed Bronchioloalveolar and Invasive Components"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Adenocarcinoma with Mixed Bronchioloalveolar and Invasive Components", "shortest_name_length": 31}
{"curie": "MONDO:0009247", "names": ["Ffnd", "FFND", "Gollop syndrome", "Frontofacionasal Dysplasia", "Frontofacionasal dysplasia", "FRONTOFACIONASAL DYSPLASIA", "frontofacionasal dysplasia", "Frontofacionasal Dysostosis", "FRONTOFACIONASAL DYSOSTOSIS", "fronto-facio-nasal dyplasia", "Frontofacionasal dysostosis", "Fronto-facio-nasal dysplasia", "fronto-facio-nasal dysostosis", "Fronto-facio-nasal dysostosis", "Frontofacionasal dysplasia syndrome", "Frontofacionasal dysplasia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontofacionasal dysplasia", "shortest_name_length": 4}
{"curie": "MONDO:0021036", "names": ["KP", "Chicken skin", "Lichen pilaris", "Carpet tack sign", "keratosis pilaris", "Keratosis pilaris", "Keratosis Pilaris", "pilaris keratosis", "Follicular plugging", "Follicular keratosis", "Hyperkeratosis pilaris", "KP - Keratosis pilaris", "Follicular keratotic plug", "Keratosis pilaris (disorder)", "keratosis pilaris (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratosis pilaris", "shortest_name_length": 2}
{"curie": "UMLS:C4725807", "names": ["Recurrent Malignant Pharyngeal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Malignant Pharyngeal Neoplasm", "shortest_name_length": 39}
{"curie": "MONDO:0005227", "names": ["ABSCESS", "abscess", "Abscess", "abscesses", "Abscesses", "Abscess NOS", "abscess (disease)", "Abscess (disorder)", "Abscess morphology", "abscess (diagnosis)", "inflammatory disorder abscess", "Abscess (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "abscess", "shortest_name_length": 7}
{"curie": "MONDO:0015400", "names": ["frontonasal arteriovenous malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontonasal arteriovenous malformation", "shortest_name_length": 38}
{"curie": "MONDO:0003374", "names": ["Larynx Leiomyosarcoma", "larynx leiomyosarcoma", "Laryngeal Leiomyosarcoma", "laryngeal leiomyosarcoma", "leiomyosarcoma of Larynx", "leiomyosarcoma of larynx", "Leiomyosarcoma of Larynx", "leiomyosarcoma of the larynx", "Leiomyosarcoma of the Larynx"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laryngeal leiomyosarcoma", "shortest_name_length": 21}
{"curie": "UMLS:C4510691", "names": ["Pneumonia caused by Chlamydia pneumoniae", "Pneumonia caused by Chlamydia pneumoniae (disorder)", "Pneumonia caused by Chlamydia pneumoniae (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pneumonia caused by Chlamydia pneumoniae", "shortest_name_length": 40}
{"curie": "UMLS:C0278544", "names": ["Dukes B rectal cancer", "stage II rectal cancer", "Rectal cancer stage II", "rectal cancer, Dukes B", "stage II rectum cancer", "Stage II Rectal Cancer", "rectum cancer, Dukes B", "rectum cancer, stage II", "rectal cancer, stage II", "Dukes B Rectal Carcinoma", "Rectal carcinoma stage II", "Carcinoma rectum stage II", "Dukes B Carcinoma of Rectum", "Carcinoma of rectum stage II", "Stage II Rectal Cancer AJCC v6", "AJCC Stage II Rectal Cancer v6", "Rectal Cancer Stage II AJCC v6", "Dukes B Carcinoma of the Rectum", "Stage II Rectal Carcinoma AJCC v6", "Stage II Carcinoma of Rectum AJCC v6", "Stage II Carcinoma of the Rectum AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Rectal Cancer", "shortest_name_length": 21}
{"curie": "UMLS:C0406801", "names": ["Eccrine angiomatous nevus", "Eccrine Angiomatous Nevus", "Eccrine angiomatous naevus", "Eccrine Angiomatous Hamartoma", "Eccrine angiomatous hamartoma", "Angiomatous Hamartoma, Eccrine", "Eccrine angiomatous hamartoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eccrine angiomatous hamartoma", "shortest_name_length": 25}
{"curie": "MONDO:0014720", "names": ["DOA+", "optic atrophy type 8", "OPTIC ATROPHY 1 AND DEAFNESS", "Treft-Sanborn-Carey syndrome", "Optic atrophy 1 and deafness", "dominant optic atrophy plus syndrome", "autosomal dominant optic atrophy plus syndrome", "optic atrophy - deafness- polyneuropathy - myopathy", "optic atrophy-deafness-polyneuropathy-myopathy syndrome", "dominant optic atrophy, deafness, ptosis, ophthalmoplegia, dystaxia, and myopathy", "optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant optic atrophy plus syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C1332187", "names": ["Brain Glioblastoma", "Adult Brain Glioblastoma", "Adult Brain Glioblastoma Multiforme"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Brain Glioblastoma", "shortest_name_length": 18}
{"curie": "MONDO:0002038", "names": ["neck carcinoma", "Neck Carcinoma", "carcinoma of neck", "Carcinoma of Neck", "head and neck cancer", "Carcinoma of the Neck", "carcinoma of the neck", "Head and Neck Carcinoma", "head and neck carcinoma", "CARCINOMA OF HEAD AND NECK", "Carcinoma of Head and Neck", "carcinoma of head and neck", "Carcinoma of the Head and Neck", "carcinoma of the head and neck", "craniocervical region carcinoma", "carcinoma of craniocervical region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "head and neck carcinoma", "shortest_name_length": 14}
{"curie": "MONDO:0000660", "names": ["akinetopsia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "akinetopsia", "shortest_name_length": 11}
{"curie": "UMLS:C1519857", "names": ["JAZF1-SUZ12 ESS", "Uterine Corpus Low Grade ESS", "JAZF1-SUZ12 Endometrial Stromal Sarcoma", "Uterine Corpus Low Grade Endometrial Stromal Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Corpus Low Grade Endometrial Stromal Sarcoma", "shortest_name_length": 15}
{"curie": "MONDO:0004588", "names": ["nyctalopia", "Nyctalopia", "NYCTALOPIA", "BLINDNESS NIGHT", "Blindness night", "Night-blindness", "Night blindness", "blindness night", "Night Blindness", "NIGHT BLINDNESS", "Blindness;night", "night blindness", "Blindness, Night", "Poor night vision", "Vision loss night", "loss night vision", "night vision loss", "VISION LOSS NIGHT", "amblyopia; nocturnal", "nocturnal; amblyopia", "Night blindness, NOS", "Night vision difficulties", "blindness; night blindness", "Night blindness (disorder)", "difficulty seeing at night", "Difficulty seeing at night", "Unspecified night blindness", "night blindness (diagnosis)", "Night blindness, unspecified", "Difficulties with night vision", "difficulty seeing at night (symptom)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "night blindness", "shortest_name_length": 10}
{"curie": "MONDO:0016524", "names": ["congenital vascular bone syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital vascular bone syndrome", "shortest_name_length": 33}
{"curie": "MONDO:0018469", "names": ["nontuberculous mycobacterial lung disease", "non-tuberculous mycobacterial lung disease", "pulmonary non-tuberculous mycobacterial infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary non-tuberculous mycobacterial infection", "shortest_name_length": 41}
{"curie": "MONDO:0100400", "names": ["AML, t(3;12)(q23;p12.3)", "acute myeloid leukemia, t(3;12)(q23;p12.3)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, t(3;12)(q23;p12.3)", "shortest_name_length": 23}
{"curie": "MONDO:0020403", "names": ["congenital mitral valve agenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital mitral valve agenesis", "shortest_name_length": 32}
{"curie": "MONDO:0011067", "names": ["DFNB12", "autosomal recessive deafness 12", "deafness, autosomal recessive 12", "DEAFNESS, AUTOSOMAL RECESSIVE 12", "Deafness, Autosomal Recessive 12", "deafness, autosomal recessive type 12", "autosomal recessive nonsyndromic deafness 12", "deafness, autosomal recessive 12, modifier of", "autosomal recessive nonsyndromic hearing loss 12", "autosomal recessive nonsyndromic deafness type 12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 12", "shortest_name_length": 6}
{"curie": "MONDO:0018333", "names": ["MADD, mild type", "MAD deficiency, mild type", "glutaric aciduria type 2, mild type", "multiple acyl-CoA dehydrogenase deficiency, mild type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple acyl-CoA dehydrogenase deficiency, mild type", "shortest_name_length": 15}
{"curie": "MONDO:0002050", "names": ["Sad", "Low Mood", "Morosity", "Low mood", "Miserable", "miserable", "depressed", "Depressed", "DEPRESSION", "depressing", "Depression", "melancholy", "depression", "Melancholy", "melancholia", "Feeling low", "Morose mood", "Melancholic", "Depressions", "melancholic", "melancholias", "Depressivity", "Feeling down", "feeling down", "Feeling;down", "Feeling blue", "MOOD DEPRESSED", "mood depressed", "Depression NOS", "depressed mood", "Decreased Mood", "Depressed Mood", "Depressed mood", "depression nos", "Mood depression", "Depressed state", "DEPRESSED STATE", "Depression, NOS", "Mood depressions", "depression moods", "Depressive state", "depressive; state", "DEPRESSION MENTAL", "state; depressive", "Depression mental", "Mental Depression", "mental depression", "Mental depression", "Depressive illness", "depression; mental", "Depression, Mental", "depressive illness", "mental; depression", "DEPRESSION PSYCHIC", "Depression, mental", "Depressive Neurosis", "Depressive disorder", "Depressive Neuroses", "DEPRESSIVE NEUROSIS", "Depressive neurosis", "depressive disorder", "depressive neurosis", "Depressive Disorder", "Neuroses, Depressive", "Disorder, Depressive", "depression (disease)", "Depression (Emotion)", "depressive; disorder", "Neurosis, depressive", "neurosis; depressive", "Depressive state NOS", "Depressive Disorders", "depression (emotion)", "Neurosis, Depressive", "depressive; neurosis", "syndrome, depressive", "disorder; depressive", "Depressive disorders", "DEPRESSIVE DISORDERS", "monopolar depression", "monopolar; depression", "syndromes, depressive", "depression; monopolar", "Disorders, Depressive", "depression (diagnosis)", "DEPRESSIVE DISORDER NOS", "Depressive disorder NOS", "Depressed mood (finding)", "Monopolar depression NOS", "Depressive disorder, NOS", "Depression, mental function", "Depressive disorder (disorder)", "depression; behavioral disorder", "Mood disorder of depressed type", "depressed mood (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "depressive disorder", "shortest_name_length": 3}
{"curie": "MONDO:0007562", "names": ["EDMMD", "Multiple epiphyseal dysplasia Beighton type", "Multiple epiphyseal dysplasia, Beighton type", "multiple epiphyseal dysplasia, Beighton type", "multiple epiphyseal dysplasia-myopia-deafness syndrome", "Multiple epiphyseal dysplasia Beighton type (disorder)", "multiple epiphyseal dysplasia with myopia and deafness", "Multiple epiphyseal dysplasia-myopia-deafness syndrome", "epiphyseal dysplasia, multiple, with myopia and deafness", "Multiple epiphyseal dysplasia-myopia-hearing loss syndrome", "Multiple epiphyseal dysplasia with myopia and deafness syndrome", "Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness", "EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MYOPIA AND CONDUCTIVE DEAFNESS", "epiphyseal dysplasia, multiple, with myopia and conductive deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple epiphyseal dysplasia, Beighton type", "shortest_name_length": 5}
{"curie": "MONDO:0100251", "names": ["HHS", "HFTC", "PHPTC", "Morbus Teutschlaender", "MORBUS TEUTSCHLAENDER", "morbus Teutschlaender", "LIPOCALCINOGRANULOMATOSIS", "Lipocalcinogranulomatosis", "lipocalcinogranulomatosis", "hyperphosphatemia hyperostosis", "Hyperphosphatemia Hyperostosis", "familial Teutschlaender disease", "Teutschlaender Disease, Familial", "hypercalcemic tumoral calcinosis", "TEUTSCHLAENDER DISEASE, FAMILIAL", "HYPEROSTOSIS WITH HYPERPHOSPHATEMIA", "hyperostosis with hyperphosphatemia", "hyperphosphatemia tumoral calcinosis", "Hyperphosphatemia Tumoral Calcinosis", "Hyperphosphatemia Hyperostosis Syndrome", "hyperphosphatemia hyperostosis syndrome", "HYPEROSTOSIS-HYPERPHOSPHATEMIA SYNDROME", "tumoral calcinosis with hyperphosphatemia", "Calcinosis, Tumoral, With Hyperphosphatemia", "CALCINOSIS, TUMORAL, WITH HYPERPHOSPHATEMIA", "cortical hyperostosis with hyperphosphatemia", "CORTICAL HYPEROSTOSIS WITH HYPERPHOSPHATEMIA", "Primary Hyperphosphatemic Tumoral Calcinosis", "primary hyperphosphatemic tumoral calcinosis", "Hyperphosphatemic Familial Tumoral Calcinosis", "TUMORAL CALCINOSIS, PRIMARY HYPERPHOSPHATEMIC", "hyperphosphatemic familial tumoral calcinosis", "Hyperphosphatemic familial tumoral calcinosis", "Tumoral Calcinosis, Primary Hyperphosphatemic", "Tumoral Calcinosis, Hyperphosphatemic, Familial", "TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL", "Hyperphosphataemic familial tumoural calcinosis", "tumoral calcinosis, hyperphosphatemic, familial, 1", "Hyperphosphatemic familial tumoral calcinosis (disorder)", "familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome", "shortest_name_length": 3}
{"curie": "EFO:0001425", "names": ["ischemic cardiomyopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ischemic cardiomyopathy", "shortest_name_length": 23}
{"curie": "UMLS:C5204615", "names": ["Bladder PEComa", "Bladder Perivascular Epithelioid Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder PEComa", "shortest_name_length": 14}
{"curie": "UMLS:C3272465", "names": ["Ampulla of Vater Invasive Papillary Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ampulla of Vater Invasive Papillary Adenocarcinoma", "shortest_name_length": 50}
{"curie": "MONDO:0010550", "names": ["CMTX2", "CMTX 2", "X-linked Charcot-Marie-Tooth disease type 2", "Charcot-Marie-Tooth disease X-linked recessive 2", "Charcot Marie Tooth disease X-linked recessive 2", "CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 2", "Charcot-Marie-Tooth disease, X-linked recessive, 2", "Charcot-Marie-Tooth neuropathy X-linked recessive 2", "Charcot-Marie-Tooth neuropathy, X-linked recessive, 2", "CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED RECESSIVE, 2", "Charcot-Marie-Tooth disease X-linked recessive type 2", "Charcot-Marie-Tooth Neuropathy, X-Linked Recessive, 2", "X-linked Charcot-Marie-Tooth disease type 2 (disorder)", "Charcot-Marie-Tooth neuropathy, X-linked recessive, 2, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease X-linked recessive 2", "shortest_name_length": 5}
{"curie": "MONDO:0018476", "names": ["dystonia-aphonia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dystonia-aphonia syndrome", "shortest_name_length": 25}
{"curie": "UMLS:C1511605", "names": ["Cystic Change", "Cystic changes", "Cystic Changes", "CYSTIC DEGENERATION", "Cystic Structures Present"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cystic Change", "shortest_name_length": 13}
{"curie": "UMLS:C4054371", "names": ["Nephrotic Syndrome - PLCE1 Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - PLCE1 Associated", "shortest_name_length": 37}
{"curie": "UMLS:C4721428", "names": ["Recurrent Sinonasal Carcinoma", "Recurrent Nasal Cavity and Paranasal Sinus Cancer", "recurrent paranasal sinus and nasal cavity cancer", "nasal cavity and paranasal sinus cancer, recurrent", "paranasal sinus and nasal cavity cancer, recurrent", "Recurrent Nasal Cavity and Paranasal Sinus Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Sinonasal Carcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0014000", "names": ["CHTD2", "TAB2 congenital heart malformation", "congenital heart defects, nonsyndromic, 2", "CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2", "congenital heart defects, multiple types, 2", "congenital heart malformation caused by mutation in TAB2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital heart defects, multiple types, 2", "shortest_name_length": 5}
{"curie": "UMLS:C0151736", "names": ["Accident Injury", "Injury, Accident", "Accidental injury", "Accidental Injury", "accidental injury", "Accident Injuries", "ACCIDENTAL INJURY", "Injury, Accidental", "Injuries, Accident", "accidental injuries", "Accidental Injuries", "Unintentional Injury", "unintentional injury", "Injuries, Accidental", "injuries unintentional", "Accidental injury (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Accidental Injuries", "shortest_name_length": 15}
{"curie": "UMLS:C5555762", "names": ["Ovarian Fibromatosis and Massive Edema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Fibromatosis and Massive Edema", "shortest_name_length": 38}
{"curie": "MONDO:0000615", "names": ["progesterone-receptor positive breast cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progesterone-receptor positive breast cancer", "shortest_name_length": 44}
{"curie": "MONDO:0033650", "names": ["MC4DN15", "mitochondrial complex 4 deficiency, nuclear type 15", "MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 15", "mitochondrial complex IV deficiency, nuclear type 15"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 4 deficiency, nuclear type 15", "shortest_name_length": 7}
{"curie": "UMLS:C5238908", "names": ["Neonatal Complication", "Neonatal Complications"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neonatal Complication", "shortest_name_length": 21}
{"curie": "UMLS:C5419608", "names": ["Advanced Transformed Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Transformed Non-Hodgkin Lymphoma", "shortest_name_length": 41}
{"curie": "MONDO:0054602", "names": ["HGPPS2", "DEVELOPMENTAL SPLIT-BRAIN SYNDROME", "gaze palsy, familial horizontal, with progressive scoliosis, 2", "GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS 2, WITH IMPAIRED INTELLECTUAL DEVELOPMENT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gaze palsy, familial horizontal, with progressive scoliosis, 2", "shortest_name_length": 6}
{"curie": "UMLS:C0948085", "names": ["Corneal defect", "corneal defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Corneal defect", "shortest_name_length": 14}
{"curie": "UMLS:C4524806", "names": ["stage IVB gastric cancer", "Stage IVB Gastric (Stomach) Cancer", "clinical stage IVB gastric cancer AJCC v8", "Clinical Stage IVB Gastric Cancer AJCC v8", "Clinical Stage IVB Gastric Carcinoma AJCC v8", "clinical stage IVB gastric carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage IVB Gastric Cancer AJCC v8", "shortest_name_length": 24}
{"curie": "MONDO:0100329", "names": ["primary viral infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary viral infectious disease", "shortest_name_length": 32}
{"curie": "UMLS:C4725878", "names": ["Unresectable Neuroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Neuroblastoma", "shortest_name_length": 26}
{"curie": "MONDO:0005153", "names": ["Adenocarcinoma", "Endocervical Cancer", "cervix adenocarcinoma", "Cervix Adenocarcinoma", "Adenocarcinoma;cervix", "adenocarcinoma cervix", "adenocarcinomas cervix", "Endocervical Carcinoma", "Carcinoma of Endocervix", "Cervical Adenocarcinoma", "adenocarcinoma - cervix", "Adenocarcinoma - cervix", "Cervical adenocarcinoma", "cervical adenocarcinoma", "Adenocarcinoma of cervix", "adenocarcinomas cervical", "adenocarcinoma of cervix", "Adenocarcinoma of Cervix", "Cervix Uteri Adenocarcinoma", "adenocarcinoma cervix uteri", "Adenocarcinoma cervix uteri", "Endocervical Adenocarcinoma", "Carcinoma of the Endocervix", "cervix uteri adenocarcinoma", "adenocarcinoma of the cervix", "Adenocarcinoma of the cervix", "Adenocarcinoma of the Cervix", "uterine cervix adenocarcinoma", "cervix cancer, adenocarcinoma", "Uterine Cervix Adenocarcinoma", "adenocarcinoma of cervix uteri", "Adenocarcinoma of Cervix Uteri", "adenocarcinoma cervical cancer", "cervical cancer, adenocarcinoma", "Adenocarcinoma of Uterine Cervix", "adenocarcinoma of uterine cervix", "Adenocarcinoma of the Cervix Uteri", "adenocarcinoma of the cervix uteri", "Adenocarcinoma of the cervix uteri", "Adenocarcinoma of cervix (disorder)", "adenocarcinoma of cervix (diagnosis)", "adenocarcinoma of the uterine cervix", "adenocarcinoma of the uterine Cervix", "Adenocarcinoma of the Uterine Cervix", "uterine cervix cancer, adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical adenocarcinoma", "shortest_name_length": 14}
{"curie": "UMLS:C0012817", "names": ["DIVERTICULA", "Diverticula", "diverticula", "DIVERTICULUM", "Diverticulum", "diverticulum", "diverticulums", "Diverticulum NOS", "Diverticulum, NOS", "Diverticulum (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diverticulum", "shortest_name_length": 11}
{"curie": "UMLS:C4683630", "names": ["St. Jude Stage II Childhood Non-Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "St. Jude Stage II Childhood Non-Hodgkin Lymphoma AJCC v8", "shortest_name_length": 56}
{"curie": "MONDO:0006455", "names": ["Thymic Undifferentiated Carcinoma", "thymic undifferentiated carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thymic undifferentiated carcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C5447241", "names": ["Breast Schwannoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Schwannoma", "shortest_name_length": 17}
{"curie": "MONDO:0012856", "names": ["BIBARS", "BIRK-BAREL SYNDROME", "Birk-Barel Syndrome", "Birk-Barel syndrome", "Intellectual disability Birk-Barel type", "intellectual disability, Birk-Barel type", "Intellectual disability, Birk-Barel type", "intellectual disabilities Birk-Barel type", "BIRK-Barel mental retardation dysmorphism syndrome", "Birk Barel mental retardation dysmorphism syndrome", "Intellectual disability Birk-Barel type (disorder)", "Birk-Barel mental retardation dysmorphism syndrome", "BIRK-BAREL MENTAL RETARDATION DYSMORPHISM SYNDROME", "Birk-Barel Mental Retardation Dysmorphism Syndrome", "Intellectual disability Birk-Barel type (diagnosis)", "BIRK-Barel intellectual disability dysmorphism syndrome", "Birk Barel intellectual disability dysmorphism syndrome", "Mental Retardation with Hypotonia and Facial Dysmorphism", "MENTAL RETARDATION WITH HYPOTONIA AND FACIAL DYSMORPHISM", "mental retardation with hypotonia and Facial Dysmorphism", "Intellectual disability-hypotonia-facial dysmorphism syndrome", "intellectual disability-hypotonia-facial dysmorphism syndrome", "intellectual disability with hypotonia and Facial Dysmorphism", "Intellectual disability, hypotonia, facial dysmorphism syndrome", "KCNK9 (potassium two pore domain channel subfamily K member 9) imprinting syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Birk-Barel syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C2828205", "names": ["Stage IV Bone Cancer", "Stage IV Bone Cancer AJCC v7", "Stage IV Bone Cancer  AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Bone Cancer AJCC v7", "shortest_name_length": 20}
{"curie": "UMLS:C5419520", "names": ["Locally Advanced Esophageal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Esophageal Adenocarcinoma", "shortest_name_length": 42}
{"curie": "UMLS:C4763784", "names": ["Refractory Primary Effusion Lymphoma", "Refractory HHV8-Positive Primary Effusion Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Primary Effusion Lymphoma", "shortest_name_length": 36}
{"curie": "UMLS:C0004403", "names": ["abnormal; autosomes", "autosomes; abnormal", "Autosome Abnormality", "Abnormality, Autosome", "Autosome Abnormalities", "Abnormalities, Autosome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Autosome Abnormalities", "shortest_name_length": 19}
{"curie": "MONDO:0009967", "names": ["RTA, DISLOCATION TYPE", "RTA, dislocation type", "bicarbonate-wasting RTA", "Bicarbonate-wasting RTA", "renal tubular acidosis 3", "Renal Tubular Acidosis III", "RENAL TUBULAR ACIDOSIS III", "renal tubular acidosis III", "RTA, bicarbonate-wasting type", "RTA, BICARBONATE-WASTING TYPE", "renal tubular acidosis, distal, type 3", "Renal tubular acidosis, distal, type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal tubular acidosis 3", "shortest_name_length": 21}
{"curie": "MONDO:0013692", "names": ["TPDS", "TPDS1", "BAP1-TPDS", "tumor predisposition syndrome", "TUMOR PREDISPOSITION SYNDROME 1", "BAP1 Tumor Predisposition Syndrome", "BAP1 tumor predisposition syndrome", "BAP1 tumour predisposition syndrome", "BAP1-related tumor predisposition syndrome", "BAP1-related tumour predisposition syndrome", "tumor susceptibility linked to germline BAP1 mutations", "Tumor susceptibility linked to germline BAP1 mutations", "BRCA1 associated protein 1 tumor predisposition syndrome", "BRCA1 associated protein 1 tumour predisposition syndrome", "Tumor susceptibility associated with germline BAP1 mutation", "Tumour susceptibility associated with germline BAP1 mutation", "BRCA1 associated protein 1 tumor predisposition syndrome (disorder)", "BRCA1 associated protein 1 tumor predisposition syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "BAP1-related tumor predisposition syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0015548", "names": ["Huntington disease-like syndrome", "Huntington's Disease Phenocopies", "Huntington Disease-Like Syndrome", "Huntington Disease-Like Syndromes", "Huntington's Disease-Like Syndromes", "Huntington disease phenocopy syndrome", "Huntington's Disease Phenocopy Syndromes", "Huntington disease-like syndrome disorder", "Huntington disease-like syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Huntington disease-like syndrome", "shortest_name_length": 32}
{"curie": "MONDO:0011428", "names": ["EEC3", "EEC syndrome 3", "EEC SYNDROME 3", "EEC Syndrome 3", "TP63 EEC syndrome", "EEC syndrome caused by mutation in TP63", "ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3", "ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3", "ectrodactyly, ectodermal dysplasia, and cleft LIP/palate syndrome 3", "Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip-Palate Syndrome 3", "ectrodactyly, ectodermal dysplasia, and cleft Lip/palate syndrome type 3", "ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3", "shortest_name_length": 4}
{"curie": "MONDO:0020248", "names": ["Vitreoretinopathy", "Vitreoretinal abnormality", "vitreoretinal degeneration", "Vitreoretinal degeneration", "Vitreoretinal abnormalities", "degenerative vitreoretinopathy", "Vitreoretinal degeneration (disorder)", "Vitreoretinal degeneration (diagnosis)", "peripheral retinal degeneration - vitreoretinal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitreoretinal degeneration", "shortest_name_length": 17}
{"curie": "UMLS:C0281870", "names": ["Stage IIIB Hodgkin Lymphoma", "Hodgkin's Disease Stage IIIB", "Stage IIIB Hodgkin's Disease", "Hodgkin's Disease Stage IIIb", "Stage IIIB Hodgkin's Lymphoma", "Hodgkin's Lymphoma Stage IIIB", "Ann Arbor Stage IIIB Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage IIIB Hodgkin Lymphoma", "shortest_name_length": 27}
{"curie": "MONDO:0030871", "names": ["VHO", "vertebral hypersegmentation and orofacial anomalies", "VERTEBRAL HYPERSEGMENTATION AND OROFACIAL ANOMALIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vertebral hypersegmentation and orofacial anomalies", "shortest_name_length": 3}
{"curie": "UMLS:C4288378", "names": ["Postoperative Spindle Cell Nodule of the Vagina"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postoperative Spindle Cell Nodule of the Vagina", "shortest_name_length": 47}
{"curie": "MONDO:0001774", "names": ["posterior scleritis", "SCLERITIS POSTERIOR", "Posterior scleritis", "scleritis posterior", "Posterior scleritis (disorder)", "posterior scleritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "posterior scleritis", "shortest_name_length": 19}
{"curie": "MONDO:0001922", "names": ["PYOURETER", "Pyoureter", "pyoureter", "ureter abscess", "Ureter abscess", "Ureter Abscess", "Ureter abscess NOS", "Pyoureter (disorder)", "pyoureter (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyoureter", "shortest_name_length": 9}
{"curie": "MONDO:0011026", "names": ["LI2", "ICR2B", "ARCI4A", "LI2, FORMERLY", "lamellar ichthyosis 2", "Ichthyosis lamellar 2", "ichthyosis lamellar 2", "ichthyosis, lamellar, 2", "Ichthyosis congenita 2B", "ichthyosis congenita 2B", "Ichthyosis, Lamellar, 2", "Ichthyosis Congenita Iib", "ICHTHYOSIS CONGENITA IIB", "ichthyosis congenita IIB", "Type 2 lamellar ichthyosis", "Lamellar ichthyosis, type 2", "lamellar ichthyosis, type 2", "ichthyosis, lamellar, 2, formerly", "ICHTHYOSIS, LAMELLAR, 2, FORMERLY", "autosomal recessive congenital ichthyosis 4A", "ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 4A", "ichthyosis, congenital, autosomal recessive 4A", "autosomal recessive congenital ichthyosis type 4A", "ichthyosis, congenital, autosomal recessive type 4A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive congenital ichthyosis 4A", "shortest_name_length": 3}
{"curie": "MONDO:0019562", "names": ["Morphea", "morphea", "keloid; Addison", "Addison; keloid", "Addison's keloid", "localized morphea", "Localized morphea", "localised morphea", "Localised morphoea", "Morphea, localized", "localised morphoea", "morphea scleroderma", "scleroderma morphea", "Morphea scleroderma", "Morphoea scleroderma", "Localised scleroderma", "Scleroderma;localised", "localised scleroderma", "Localized scleroderma", "scleroderma localized", "Localized Scleroderma", "localized scleroderma", "Scleroderma, Localized", "scleroderma; localized", "Scleroderma, localized", "localized; scleroderma", "Sclerodermas, Localized", "Scleroderma circumscribed", "Circumscribed Scleroderma", "Circumscribed scleroderma", "circumscribed scleroderma", "SCLERODERMA CIRCUMSCRIBED", "Scleroderma, Circumscribed", "Localised dermatosclerosis", "Localized dermatosclerosis", "scleroderma; circumscribed", "circumscribed; scleroderma", "localized; dermatosclerosis", "dermatosclerosis; localized", "Dermatosclerosis, localized", "Localized morphea (disorder)", "localized scleroderma morphea", "morphea (localized scleroderma)", "Localised scleroderma [morphea]", "localized fibrosing scleroderma", "Localized scleroderma [morphea]", "Localized fibrosing scleroderma", "Scleroderma, circumscribed or localised", "Scleroderma, circumscribed or localized", "Circumscribed scleroderma, localized type", "localized scleroderma (disorder) [ambiguous]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "localized scleroderma", "shortest_name_length": 7}
{"curie": "UMLS:C5239335", "names": ["Metastatic Bladder Urachal Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Bladder Urachal Urothelial Carcinoma", "shortest_name_length": 47}
{"curie": "UMLS:C4683597", "names": ["Lugano Classification Stage IE Childhood Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage IE Childhood Hodgkin Lymphoma AJCC v8", "shortest_name_length": 65}
{"curie": "UMLS:C0579142", "names": ["opiate overdose", "OPIATE OVERDOSE", "Opiate Overdose", "Opioid Overdose", "Opiate Overdoses", "Overdose, Opioid", "Overdose, Opiate", "Opioid Overdoses", "Narcotic overdose", "Overdose of opiate", "Overdose of opiate (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Opiate Overdose", "shortest_name_length": 15}
{"curie": "UMLS:C4727073", "names": ["Recurrent Mediastinal Lymphoma", "Recurrent Primary Mediastinal Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Mediastinal Lymphoma", "shortest_name_length": 30}
{"curie": "MONDO:0016174", "names": ["paraneoplastic sensory neuronopathy", "paraneoplastic sensory ganglionopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paraneoplastic sensory ganglionopathy", "shortest_name_length": 35}
{"curie": "MONDO:0014110", "names": ["CTRCT15", "cataract 15 multiple types", "cataract 15, multiple types", "CATARACT 15, MULTIPLE TYPES", "MIP early-onset non-syndromic cataract", "early-onset non-syndromic cataract caused by mutation in MIP"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 15 multiple types", "shortest_name_length": 7}
{"curie": "UMLS:C4525664", "names": ["Stage IV Ileal Neuroendocrine Tumor", "Stage IV Ileal Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Ileal Neuroendocrine Tumor AJCC v8", "shortest_name_length": 35}
{"curie": "UMLS:C0206171", "names": ["Community Acquired Infection", "community-acquired infection", "Community-Acquired Infection", "Community acquired infection", "Community Acquired Infections", "Infection, Community Acquired", "Infection, Community-Acquired", "Community-acquired infections", "Community-Acquired Infections", "community acquired infections", "Acquired Infection, Community", "Infections, Community-Acquired", "Infections, Community Acquired", "Acquired Infections, Community"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Community-Acquired Infections", "shortest_name_length": 28}
{"curie": "UMLS:C1963828", "names": ["Uterine cervix stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine cervix stenosis", "shortest_name_length": 23}
{"curie": "MONDO:0700073", "names": ["GA2A", "ETFA deficiency", "glutaric acidemia 2A", "glutaric acidemia IIa", "multiple acyl-CoA dehydrogenase deficiency caused by mutation in ETFA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glutaric acidemia IIa", "shortest_name_length": 4}
{"curie": "MONDO:0030089", "names": ["PNDM4", "DIABETES MELLITUS, PERMANENT NEONATAL 4", "diabetes mellitus, permanent neonatal 4", "DIABETES MELLITUS, PERMANENT NEONATAL, 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diabetes mellitus, permanent neonatal 4", "shortest_name_length": 5}
{"curie": "UMLS:C3272609", "names": ["Colorectal MANEC", "Colorectal Mixed Adenoneuroendocrine Carcinoma", "Colorectal (Colon or Rectal) Mixed Adenoneuroendocrine Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Mixed Adenoneuroendocrine Carcinoma", "shortest_name_length": 16}
{"curie": "MONDO:0014829", "names": ["ICF4", "ICF syndrome 4", "IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 4", "immunodeficiency-centromeric instability-Facial anomalies syndrome 4", "immunodeficiency-centromeric instability-facial anomalies syndrome 4", "immunodeficiency-centromeric instability-FACIAL anomalies syndrome 4", "HELLS immunodeficiency-centromeric instability-facial anomalies syndrome", "immunodeficiency-centromeric instability-facial anomalies syndrome type 4", "immunodeficiency-centromeric instability-Facial anomalies syndrome type 4", "immunodeficiency-centromeric instability-facial anomalies syndrome caused by mutation in HELLS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency-centromeric instability-facial anomalies syndrome 4", "shortest_name_length": 4}
{"curie": "MONDO:0017236", "names": ["RPGN", "acute RPGN", "crescentic glomerulonephritis", "rapidly progressive glomerulitis", "Rapidly Progressive Glomerulonephritis", "Glomerulonephritis rapidly progressive", "GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE", "Rapidly progressive glomerulonephritis", "rapidly progressive glomerulonephritis", "rapidly progressive; glomerulonephritis", "Glomerulonephritis, rapidly progressive", "glomerulonephritis; rapidly progressive", "GLOMERULONEPHRITIS, RAPIDLY PROGRESSIVE", "nephropathy rapidly progressive glomerulitis", "acute rapidly progressive glomerulonephritis", "rapidly progressive acute glomerulonephritis", "rapidly progressive glomerulitis (diagnosis)", "RPGN - Rapidly progressive glomerulonephritis", "Rapidly progressive glomerulonephritis syndrome", "Rapidly progressive glomerulonephritis (disorder)", "acute rapidly progressive glomerulonephritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rapidly progressive glomerulonephritis", "shortest_name_length": 4}
{"curie": "UMLS:C0854796", "names": ["Unresectable Hepatoblastoma", "Hepatoblastoma, Nonresectable", "Hepatoblastoma non-resectable", "Non-Resectable Hepatoblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatoblastoma non-resectable", "shortest_name_length": 27}
{"curie": "MONDO:0004649", "names": ["anaerobic pneumonia", "anaerobes pneumonia", "pneumonia due to anaerobes", "Pneumonia due to anaerobes", "PNEUMONIA BACTERIAL ANAEROBIC", "Pneumonia anaerobic bacterial NOS", "pneumonia due to anaerobic bacteria", "Pneumonia due to anaerobic bacteria", "Pneumonia caused by anaerobic bacteria", "pneumonia caused by anaerobic bacteria", "pneumonia due to anaerobic bacteria (diagnosis)", "Pneumonia caused by anaerobic bacteria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anaerobic pneumonia", "shortest_name_length": 19}
{"curie": "MONDO:0020579", "names": ["Mucitis", "mucitis", "mucosity", "mucositis", "Mucositis", "MUCOSITIS", "Mucositides", "Mucitis, NOS", "Mucositis NOS", "MUCOSITIS NOS", "Mucositis, NOS", "mucosa inflammation", "Mucous inflammation", "MUCOSAL INFLAMMATION", "mucosal inflammation", "Mucosal inflammation", "mucositis (diagnosis)", "inflammation of mucosa", "Catarrhal inflammation", "Mucous inflammation, NOS", "Mucosal inflammation NOS", "Mucosal inflammation, NOS", "Catarrhal inflammation, NOS", "INFLAMMATION MUCOUS MEMBRANE", "Inflammation mucous membrane", "Mucous membrane inflammation", "MUCOUS MEMBRANE INFLAMMATION", "Mucous membrane inflammation, NOS", "Inflammatory disease of mucous membrane", "Mucous inflammation (morphologic abnormality)", "Inflammatory disease of mucous membrane (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucositis", "shortest_name_length": 7}
{"curie": "MONDO:0000200", "names": ["ZLS", "ZLS1", "laband syndrome", "LABAND SYNDROME", "Laband syndrome", "Zimmerman Laband syndrome", "Zimmermann-Laband syndrome", "zimmermann-laband syndrome", "Laband-Zimmermann syndrome", "Zimmermann-Laband Syndrome", "Zimmermann-Laband syndrome 1", "Zimmermann-Laband syndrome (ZLS)", "Zimmermann-Laband syndrome type 1", "Zimmermann-Laband syndrome (disorder)", "fibromatosis gingival, hepatosplenomegaly other anomalies", "Gingival fibromatosis-hepatosplenomegaly-other anomalies syndrome", "gingival fibromatosis-hepatosplenomegaly-other anomalies syndrome", "gingival fibromatosis, abnormal fingers, fingernails, nose and ears, and splenomegaly", "Fibromatosis, Gingival, With Abnormal Fingers, Fingernails, Nose And Ears, And Splenomegaly", "FIBROMATOSIS, GINGIVAL, WITH ABNORMAL FINGERS, FINGERNAILS, NOSE, AND EARS, AND SPLENOMEGALY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Zimmermann-Laband syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C5239043", "names": ["Very High Risk Chronic Myelogenous Leukemia, BCR-ABL1 Positive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Very High Risk Chronic Myelogenous Leukemia, BCR-ABL1 Positive", "shortest_name_length": 62}
{"curie": "MONDO:0018993", "names": ["CMT2", "Charcot-Marie-Tooth type 2", "hereditary peripheral neuropathy", "Peripheral neuropathy hereditary", "Hereditary peripheral neuropathy", "Charcot-Marie-Tooth disease type 2", "Hereditary peripheral neuropathy, NOS", "Hereditary peripheral neuropathy (disorder)", "hereditary peripheral neuropathy (diagnosis)", "hereditary motor and sensory neuropathy type 2", "hereditary motor and sensory neuropathy Okinawa type", "autosomal dominant Charcot-Marie-Tooth disease type 2", "autosomal dominant axonal Charcot-Marie-Tooth disease", "hereditary motor and sensory neuropathy Guadalajara neuronal type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 2", "shortest_name_length": 4}
{"curie": "MONDO:0017629", "names": ["sodium channelopathy-related small fiber neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sodium channelopathy-related small fiber neuropathy", "shortest_name_length": 51}
{"curie": "MONDO:0020180", "names": ["palpebral piliary tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "palpebral piliary tumor", "shortest_name_length": 23}
{"curie": "MONDO:0016752", "names": ["BPNST", "benign peripheral nerve sheath tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign peripheral nerve sheath tumor", "shortest_name_length": 5}
{"curie": "MONDO:0018875", "names": ["LFS", "Li-Fraumeni", "SBLA syndrome", "SBLA SYNDROME", "Li Fraumeni Syndrome", "Li-Fraumeni Syndrome", "li fraumeni syndrome", "Li-Fraumeni syndrome", "LI-FRAUMENI SYNDROME", "li-fraumeni syndrome", "Li Fraumeni syndrome", "Li-Fraumeni syndrome (disorder)", "Li-Fraumeni syndrome (diagnosis)", "TP53-Associated Li-Fraumeni Syndrome", "Li-Fraumeni Syndrome, TP53-Associated", "SARCOMA FAMILY SYNDROME OF LI AND FRAUMENI", "sarcoma family syndrome of Li and Fraumeni", "Li-Fraumeni Familial Cancer Susceptibility Syndrome", "Li-Fraumeni familial cancer susceptibility syndrome", "Li-Fraumeni Familiar Cancer Susceptibility Syndrome", "Li-Fraumeni Familiar cancer Susceptibility syndrome", "Li-Fraumeni familiar cancer susceptibility syndrome", "sarcoma, breast, leukaemia and adrenal gland syndrome", "SBLA syndrome (sarcoma, breast, leukemia, and adrenal gland)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Li-Fraumeni syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C0854725", "names": ["cyanopsia", "Cyanopsia", "Blue vision", "blue vision"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cyanopsia", "shortest_name_length": 9}
{"curie": "UMLS:C5420056", "names": ["Sinonasal Solitary Fibrous Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Solitary Fibrous Tumor", "shortest_name_length": 32}
{"curie": "UMLS:C1335794", "names": ["Round Cell Liposarcoma NCI Grade 3", "Round Cell Liposarcoma NCI Grade III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Round Cell Liposarcoma NCI Grade 3", "shortest_name_length": 34}
{"curie": "MONDO:0010949", "names": ["CMT2B", "HMSN2B", "CMT 2B", "HMSN IIB", "Charcot-Marie-Tooth disease type 2B", "Charcot Marie Tooth disease type 2B", "Charcot-Marie-Tooth disease Type 2B", "Charcot-Marie-Tooth disease, type 2B", "Charcot-Marie-Tooth disease, Type 2B", "Charcot-Marie-Tooth neuropathy type 2B", "Charcot-Marie-Tooth neuropathy, type 2B", "Charcot-Marie-Tooth Neuropathy, Type 2B", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2B", "RAB7A Charcot-Marie-Tooth disease type 2", "hereditary motor and sensory neuropathy 2B", "hereditary motor and sensory nueropathy IIB", "Hereditary Motor And Sensory Neuropathy IIB", "HEREDITARY MOTOR AND SENSORY NEUROPATHY IIB", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B", "Charcot-Marie-Tooth disease, axonal, type 2B", "Charcot-Marie-Tooth disease, axonal, Type 2B", "Charcot-Marie-Tooth disease, neuronal, Type 2B", "Charcot-Marie-Tooth disease, neuronal, type 2B", "Charcot-Marie-Tooth disease Type 2B (diagnosis)", "Hereditary motor and sensory neuropathy 2 B (HMSN 2 B)", "autosomal dominant Charcot-Marie-Tooth disease type 2B", "Autosomal dominant Charcot-Marie-Tooth disease type 2B", "hereditary motor and sensory neuropathy 2 B (HMSN 2 B)", "peripheral sensory neuropathy, autosomal dominant (PSN)", "Peripheral sensory neuropathy, autosomal dominant (PSN)", "CHARCOT-MARIE-TOOTH DISEASE, AUTOSOMAL DOMINANT, TYPE 2B", "Charcot-Marie-Tooth Disease, Autosomal Dominant, Type 2B", "Charcot-Marie-Tooth disease, autosomal dominant, type 2B", "Charcot-Marie-Tooth disease type 2 caused by mutation in RAB7A", "Autosomal dominant Charcot-Marie-Tooth disease type 2B (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 2B", "shortest_name_length": 5}
{"curie": "MONDO:0016880", "names": ["partial deletion of chromosome 18", "partial monosomy of chromosome 18", "partial deletion of chromosome type 18"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of chromosome 18", "shortest_name_length": 33}
{"curie": "MONDO:0014838", "names": ["CSS5", "Coffin-Siris syndrome 5", "COFFIN-SIRIS syndrome 5", "COFFIN-SIRIS SYNDROME 5", "Coffin-Siris syndrome type 5", "SMARCE1 Coffin-Siris syndrome", "Coffin-Siris syndrome caused by mutation in SMARCE1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Coffin-Siris syndrome 5", "shortest_name_length": 4}
{"curie": "UMLS:C4520916", "names": ["Stage IB Soft Tissue Sarcoma", "Stage IB Adult Sarcoma of Soft Tissue", "Stage IB Adult Sarcoma of the Soft Tissue", "Stage IB Adult Soft Tissue Sarcoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Adult Soft Tissue Sarcoma AJCC v7", "shortest_name_length": 28}
{"curie": "MONDO:0018754", "names": ["cyanide poison", "poisoning cyanide", "CYANIDE POISONING", "cyanide poisoning", "Cyanide poisoning", "poisoning by cyanide", "Toxic effect of cyanide", "Toxic effect of cyanides", "Cyanide poisoning syndrome", "Toxic effect of cyanide, NOS", "Toxic effect of cyanides NOS", "Cyanides causing toxic effect", "poisoning by cyanide (diagnosis)", "Toxic effect of cyanide (disorder)", "Cyanides and hydrocyanic acid causing toxic effect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cyanide poisoning", "shortest_name_length": 14}
{"curie": "MONDO:0700182", "names": ["Feline Erythroleukemia", "feline erythroleukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "feline erythroleukemia", "shortest_name_length": 22}
{"curie": "MONDO:0700037", "names": ["testicular fibrothecoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular fibrothecoma", "shortest_name_length": 23}
{"curie": "UMLS:C1336307", "names": ["Stage II Osteosarcoma", "Stage II Osteogenic Sarcoma", "Stage II Osteosarcoma AJCC v7", "Stage II Osteosarcoma  AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Osteosarcoma AJCC v7", "shortest_name_length": 21}
{"curie": "UMLS:C1519195", "names": ["Schistosoma Hematobium-Related Bladder Verrucous Carcinoma", "Schistosoma Hematobium-Related Bladder Verrucous Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Schistosoma Hematobium-Related Bladder Verrucous Carcinoma", "shortest_name_length": 58}
{"curie": "MONDO:0015346", "names": ["EMEA", "Jeavons syndrome", "Jeavons syndrome (disorder)", "Jeavons syndrome (diagnosis)", "epilepsy with eyelid myoclonias", "epilepsy reflex Jeavons syndrome", "Eyelid myoclonia with and without absences", "eyelid myoclonia with and without absences"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jeavons syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C1336424", "names": ["Stage IV Major Salivary Gland Cancer with Metastasis", "Stage IV Major Salivary Gland Carcinoma with Metastasis", "Stage IV Carcinoma of Major Salivary Gland with Metastasis", "Stage IV Carcinoma of the Major Salivary Gland with Metastasis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Major Salivary Gland Carcinoma with Metastasis", "shortest_name_length": 52}
{"curie": "UMLS:C1336229", "names": ["Stage IIIB Retinoblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Retinoblastoma", "shortest_name_length": 25}
{"curie": "UMLS:C0151555", "names": ["Cinchonism", "CINCHONISM", "Cinchonism, NOS", "Cinchonism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cinchonism (disorder)", "shortest_name_length": 10}
{"curie": "UMLS:C1096187", "names": ["Implant site bleeding", "Implant site hemorrhage", "Implant site haemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Implant site hemorrhage", "shortest_name_length": 21}
{"curie": "MONDO:0005918", "names": ["PLACENTA PREVIA", "Placenta Previa", "Placenta previa", "previa placenta", "placenta previa", "Placenta Praevia", "previa; placenta", "PLACENTA PRAEVIA", "placenta praevia", "placenta; previa", "Placenta praevia", "Placenta previa NOS", "Placenta previa, NOS", "PP - Placenta previa", "PP - Placenta praevia", "Placenta praevia, NOS", "Placenta previa (disorder)", "placenta previa (diagnosis)", "placenta previa was observed", "placenta previa (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "placenta praevia", "shortest_name_length": 15}
{"curie": "MONDO:0008609", "names": ["Tristichiasis", "TRISTICHIASIS", "Triple row of eyelashes", "Three rows of eyelashes", "eyelashes, three rows of", "EYELASHES, THREE ROWS OF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tristichiasis", "shortest_name_length": 13}
{"curie": "MONDO:0019104", "names": ["sandifer syndrome", "Sandifer syndrome", "Sandifer Syndrome", "sandifers syndrome", "Sandifer's syndrome", "Sandifer's Syndrome", "sandifer's syndrome", "Sandifer syndrome (disorder)", "Contortions of the neck and abnormal postures in congenital hiatus hernia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sandifer syndrome", "shortest_name_length": 17}
{"curie": "MONDO:0018370", "names": ["KLHL9-related early-onset distal myopathy", "Kelch like family member 9 related early-onset distal myopathy", "Kelch like family member 9 related early-onset distal myopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "KLHL9-related early-onset distal myopathy", "shortest_name_length": 41}
{"curie": "UMLS:C0334527", "names": ["Choriocarcinoma combined with germ cell elements", "Choriocarcinoma combined with embryonal carcinoma", "Choriocarcinoma combined with other germ cell elements", "Choriocarcinoma Combined with Other Germ Cell Elements", "choriocarcinoma combined with other germ cell elements", "choriocarcinoma combined with other germ cell elements (diagnosis)", "Choriocarcinoma combined with other germ cell elements (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Choriocarcinoma combined with other germ cell elements", "shortest_name_length": 48}
{"curie": "MONDO:0002307", "names": ["Blepharoconjunctivitis", "blepharoconjunctivitis", "BLEPHAROCONJUNCTIVITIS", "Blepharo conjunctivitis", "BLEPHARO CONJUNCTIVITIS", "Blepharoconjunctivitis, NOS", "Blepharoconjunctivitis (disorder)", "blepharoconjunctivitis (diagnosis)", "Unspecified blepharoconjunctivitis", "Blepharoconjunctivitis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blepharoconjunctivitis", "shortest_name_length": 22}
{"curie": "MONDO:0014631", "names": ["HOMGSMR", "HOMGSMR1", "hypomagnesemia, seizures, and mental retardation", "HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION 1", "hypomagnesemia, seizures, and intellectual disability", "HYPOMAGNESEMIA, SEIZURES, AND IMPAIRED INTELLECTUAL DEVELOPMENT 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypomagnesemia, seizures, and intellectual disability", "shortest_name_length": 7}
{"curie": "MONDO:0007261", "names": ["Carabelli Anomaly of Maxillary Molar Teeth", "Carabelli anomaly of maxillary molar teeth", "CARABELLI ANOMALY OF MAXILLARY MOLAR TEETH"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carabelli anomaly of maxillary molar teeth", "shortest_name_length": 42}
{"curie": "UMLS:C4054578", "names": ["Malignant Hypertensive Nephropathy", "Accelerated Hypertensive Nephropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Hypertensive Nephropathy", "shortest_name_length": 34}
{"curie": "UMLS:C0269002", "names": ["bleed penis", "bleeds penis", "bleeding penis", "penis bleeding", "PENIS BLEEDING", "Penis bleeding", "Penile bleeding", "penile bleeding", "Penile Bleeding", "penis hemorrhage", "hemorrhage; penis", "penile hemorrhage", "penis; hemorrhage", "Penile hemorrhage", "PENILE HEMORRHAGE", "PENILE HAEMORRHAGE", "Penile haemorrhage", "Hemorrhage of penis", "hemorrhage of penis", "Haemorrhage of penis", "Hemorrhage of penis (disorder)", "hemorrhage of penis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemorrhage of penis", "shortest_name_length": 11}
{"curie": "MONDO:0002624", "names": ["Bone Leiomyosarcoma", "bone leiomyosarcoma", "Leiomyosarcoma of Bone", "leiomyosarcoma of bone", "bone tissue leiomyosarcoma", "leiomyosarcoma of bone tissue", "leiomyosarcoma of bone (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bone leiomyosarcoma", "shortest_name_length": 19}
{"curie": "UMLS:C0032792", "names": ["Shock;post-op", "post-op shock", "Postoperative shock", "postoperative shock", "Postoperative Shock", "shock; postoperative", "postoperative; shock", "postoperative; collapse", "collapse; postoperative", "Postoperative shock, NOS", "Postoperative shock (disorder)", "postoperative shock (diagnosis)", "Postoperative shock, unspecified", "Shock during or resulting from a surgical procedure", "Shock, NOS, during or resulting from a surgical procedure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postoperative shock", "shortest_name_length": 13}
{"curie": "MONDO:0030374", "names": ["WHIMS2", "WHIM syndrome 2", "WHIM SYNDROME 2", "WARTS, HYPOGAMMAGLOBULINEMIA, INFECTIONS, AND MYELOKATHEXIS SYNDROME 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "WHIM syndrome 2", "shortest_name_length": 6}
{"curie": "MONDO:0037847", "names": ["spondyloarthropathy", "vertebral joint disease", "vertebral joint disorder", "disorder of joint of spine", "intervertebral joint disease", "disease of intervertebral joint", "disorder of intervertebral joint", "intervertebral joint disease or disorder", "disease or disorder of intervertebral joint"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vertebral joint disorder", "shortest_name_length": 19}
{"curie": "MONDO:0001967", "names": ["DYSGENETIC_GONAD", "Gonadal dysgenesis", "gonadal dysgenesis", "GONADAL DYSGENESIS", "Gonadal Dysgenesis", "dysgenesis; gonadal", "gonadal; dysgenesis", "Dysgenesis, Gonadal", "Gonadal dysgenesis NOS", "Pure gonadal dysgenesis", "pure gonadal dysgenesis", "Mixed gonadal dysgenesis", "gonadal; dysgenesis, pure", "dysgenesis; gonadal, pure", "gonadal dysgenesis syndrome", "Gonadal dysgenesis syndrome", "Pure gonadal dysgenesis, NOS", "Gonadal dysgenesis (disorder)", "Pure gonadal dysgenesis (disorder)", "pure gonadal dysgenesis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gonadal dysgenesis", "shortest_name_length": 16}
{"curie": "MONDO:0008598", "names": ["trichodysplasia xeroderma", "Trichodysplasia-Xeroderma", "TRICHODYSPLASIA-XERODERMA", "trichodysplasia-xeroderma", "trichodysplasia-xeroderma syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichodysplasia-xeroderma syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0014519", "names": ["Monge", "Monge disease", "Andes disease", "MONGE DISEASE", "Monges disease", "Andes; disease", "Monge's disease", "monge's disease", "Mountain sickness chronic", "Chronic mountain sickness", "chronic mountain sickness", "disease (or disorder); Andes", "Chronic mountain sickness (disorder)", "chronic mountain sickness (diagnosis)", "chronic mountain sickness, susceptibility to", "CHRONIC MOUNTAIN SICKNESS, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic mountain sickness, susceptibility to", "shortest_name_length": 5}
{"curie": "MONDO:0017081", "names": ["encephalocele parietal", "parietal encephalocele", "Parietal encephalocele", "Parietal encephalocele (disorder)", "Parietal encephalocele (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parietal encephalocele", "shortest_name_length": 22}
{"curie": "MONDO:0700112", "names": ["SIV", "HTX5", "SIV, FORMERLY", "situs inversus viscerum", "NODAL visceral heterotaxy", "SITUS INVERSUS VISCERUM, FORMERLY", "heterotaxy, visceral, 5, autosomal", "HETEROTAXY, VISCERAL, 5, AUTOSOMAL", "Heterotaxy, Visceral, 5, Autosomal", "visceral heterotaxy caused by mutation in NODAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heterotaxy, visceral, 5, autosomal", "shortest_name_length": 3}
{"curie": "MONDO:0026426", "names": ["SXI2", "X Inactivation, Familial Skewed, 2", "X-inactivation, familial skewed, 2", "X INACTIVATION, FAMILIAL SKEWED, 2", "X inactivation, familial skewed, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X inactivation, familial skewed, 2", "shortest_name_length": 4}
{"curie": "UMLS:C0863168", "names": ["Adenocarcinoma gastric recurrent", "Recurrent Gastric Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma gastric recurrent", "shortest_name_length": 32}
{"curie": "UMLS:C0280145", "names": ["intermediate-grade, stage II adult NHL", "NHL, intermediate grade, stage II adult", "adult NHL, stage II, intermediate grade", "Stage II Intermediate Grade Adult Non-Hodgkin's Lymphoma", "non-Hodgkin's lymphoma, intermediate grade, stage II adult", "lymphoma, intermediate grade, stage II adult non-Hodgkin's", "adult non-Hodgkin's lymphoma, intermediate grade, stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Intermediate Grade Adult Non-Hodgkin's Lymphoma", "shortest_name_length": 38}
{"curie": "MONDO:0054805", "names": ["MCPH22", "microcephaly 22, primary, autosomal recessive", "microcephaly 22, PRIMARY, autosomal recessive", "MICROCEPHALY 22, PRIMARY, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly 22, primary, autosomal recessive", "shortest_name_length": 6}
{"curie": "MONDO:0001016", "names": ["epididymis cancer", "Epididymal cancer", "cancer of epididymis", "malignant epididymal tumor", "malignant Epididymal tumor", "Malignant Epididymal Tumor", "malignant epididymal neoplasm", "Malignant Tumor of Epididymis", "malignant tumor of epididymis", "Malignant Epididymal Neoplasm", "malignant epididymis neoplasm", "Malignant tumor of epididymis", "Malignant tumour of epididymis", "malignant neoplasm of epididymis", "Malignant Neoplasm of Epididymis", "Malignant neoplasm of epididymis", "malignant tumor of the epididymis", "Malignant epididymal neoplasm NOS", "Malignant Tumor of the Epididymis", "Malignant Neoplasm of the Epididymis", "malignant neoplasm of the epididymis", "Malignant tumor of epididymis (disorder)", "malignant neoplasm of epididymis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epididymis cancer", "shortest_name_length": 17}
{"curie": "MONDO:0022930", "names": ["Aughton Sloan Milad syndrome", "Aughton sloan Milad syndrome", "Nasopharyngeal teratoma with Dandy Walker diaphragmatic hernia", "Dandy-Walker malformation with nasopharyngeal teratoma and diaphragmatic hernia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dandy-Walker malformation with nasopharyngeal teratoma and diaphragmatic hernia", "shortest_name_length": 28}
{"curie": "MONDO:0018553", "names": ["Urachal Diverticulum", "urachal diverticulum", "Urachal diverticulum", "Vesicourachal diverticulum", "Urachal diverticulum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urachal diverticulum", "shortest_name_length": 20}
{"curie": "UMLS:C5420196", "names": ["Refractory Mature T-Cell and NK-Cell Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Mature T-Cell and NK-Cell Neoplasm", "shortest_name_length": 45}
{"curie": "UMLS:C2347757", "names": ["Childhood Classic Hodgkin Lymphoma", "Childhood Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Classic Hodgkin Lymphoma", "shortest_name_length": 34}
{"curie": "MONDO:0010713", "names": ["PFD", "CFPD", "Properdin deficiency", "Properdin deficiency, type 1", "Properdin deficiency disease", "properdin deficiency, type 1", "Properdin Deficiency, Type I", "properdin deficiency, type 3", "properdin deficiency disease", "properdin deficiency, type 2", "PROPERDIN DEFICIENCY, TYPE I", "PROPERDIN DEFICIENCY, TYPE II", "X-linked properdin deficiency", "Properdin P factor deficiency", "properdin P Factor deficiency", "PROPERDIN P FACTOR DEFICIENCY", "Properdin Deficiency, Type II", "Properdin Deficiency, Type III", "PROPERDIN DEFICIENCY, TYPE III", "Properdin deficiency, X-linked", "PROPERDIN DEFICIENCY, X-LINKED", "properdin deficiency, X-linked", "complement Factor properdin deficiency", "complement factor properdin deficiency", "COMPLEMENT FACTOR PROPERDIN DEFICIENCY", "Properdin deficiency disease (disorder)", "properdin deficiency disease (diagnosis)", "properdin deficiency, X-linked, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "properdin deficiency, X-linked", "shortest_name_length": 3}
{"curie": "MONDO:0014085", "names": ["HYC2", "MPDZ congenital hydrocephalus", "hydrocephalus, nonsyndromic, autosomal recessive 2", "congenital hydrocephalus caused by mutation in MPDZ", "hydrocephalus, nonsyndromic, autosomal recessive type 2", "HYDROCEPHALUS, NONSYNDROMIC, AUTOSOMAL RECESSIVE 2, FORMERLY", "HYDROCEPHALUS, CONGENITAL, 2, WITH OR WITHOUT BRAIN OR EYE ANOMALIES", "hydrocephalus, congenital, 2, with or without brain or eye anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hydrocephalus, nonsyndromic, autosomal recessive 2", "shortest_name_length": 4}
{"curie": "UMLS:C0857183", "names": ["Pre-menstrual tension syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pre-menstrual tension syndrome", "shortest_name_length": 30}
{"curie": "MONDO:0030747", "names": ["JEB2B", "epidermolysis bullosa, junctional 2B, severe", "EPIDERMOLYSIS BULLOSA, JUNCTIONAL 2B, SEVERE", "epidermolysis bullosa, junctional 2B, herlitz IIA", "EPIDERMOLYSIS BULLOSA, JUNCTIONAL 2B, HERLITZ TYPE", "EPIDERMOLYSIS BULLOSA, JUNCTIONAL 2B, GENERALIZED SEVERE", "epidermolysis bullosa, junctional 2B, generalized severe"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolysis bullosa, junctional 2B, severe", "shortest_name_length": 5}
{"curie": "MONDO:0008410", "names": ["Calvé", "Scheuermann", "Calve disease", "Calve's disease", "Calve's Disease", "Calvé's disease", "Sherman's Disease", "Juvenile kyphosis", "Juvenile Kyphosis", "Juvenile Kyphoses", "Sherman's disease", "juvenile kyphosis", "Kyphosis, Juvenile", "Morbus Scheuermann", "Kyphoses, Juvenile", "scheuermann disease", "Adolescent Kyphosis", "Adolescent Kyphoses", "Scheuermann disease", "Scheuermann Disease", "SCHEUERMANN DISEASE", "Disease;Scheuermann", "Scheuermanns Disease", "SCHUERMANN'S DISEASE", "Scheuermann Kyphoses", "scheuermanns disease", "Kyphoses, Adolescent", "schuermann's disease", "Kyphosis, Adolescent", "Scheurmann's Disease", "Scheuermann Kyphosis", "scheurmann's disease", "Scheuermann kyphosis", "diseases scheuermanns", "scheuermann's disease", "Scheuermann's disease", "Scheuermanns Kyphosis", "disease scheuermann's", "Scheuermann's Disease", "Kyphosis, Scheuermann", "Kyphoses, Scheuermann", "vertebral epiphysitis", "Vertebral epiphysitis", "Scheuermann's kyphosis", "scheuermann's kyphosis", "Scheuermann's Kyphoses", "SPINAL OSTEOCHONDROSIS", "spinal Osteochondrosis", "Scheuermann's Kyphosis", "Kyphosis, Scheuermann's", "Kyphoses, Scheuermann's", "Osteochondritis of spine", "Adolescent Hyperkyphosis", "Adolescent Hyperkyphoses", "Hyperkyphosis, Adolescent", "Hyperkyphoses, Adolescent", "Kyphosis dorsalis juvenilis", "familial Scheuermann disease", "osteochondrosis; Scheuermann", "Scheuermann; osteochondrosis", "Osteochondritis of the spine", "Scheuermann juvenile kyphosis", "Scheuermann Juvenile Kyphosis", "SCHEUERMANN JUVENILE KYPHOSIS", "Scheuermann Juvenile Kyphoses", "Spine Juvenile Osteochondrosis", "Kyphoses, Scheuermann Juvenile", "Spine Juvenile Osteochondroses", "Juvenile Kyphosis, Scheuermann", "Juvenile Kyphoses, Scheuermann", "Kyphosis, Scheuermann Juvenile", "familial spinal osteochondrosis", "spine; osteochondrosis, juvenile", "Juvenile Osteochondrosis of Spine", "Juvenile osteochondrosis of spine", "juvenile osteochondrosis of spine", "vertebra; osteochondrosis, juvenile", "osteochondrosis; juvenile, vertebra", "juvenile osteochondritis of the spine", "Juvenile osteochondrosis of spine NOS", "Juvenile osteochondrosis of the spine", "Juvenile osteochondritis of the spine", "Juvenile osteochondrosis of spine, NOS", "familial Scheuermann juvenile kyphosis", "Juvenile osteochondrosis of Scheurermann", "juvenile osteochondrosis of Scheurermann", "spine or vertebra; osteochondrosis, juvenile", "osteochondrosis; spine or vertebra, juvenile", "Juvenile osteochondrosis of spine (disorder)", "juvenile osteochondrosis of spine (diagnosis)", "Juvenile osteochondrosis of vertebral epiphyses", "juvenile osteochondrosis of vertebral epiphyses", "Juvenile osteochondrosis of spine, site unspecified", "vertebra; osteochondrosis epiphyseal plates, juvenile", "epiphyseal; plates, vertebral, juvenile osteochondrosis", "juvenile osteochondrosis of vertebral epiphyses (diagnosis)", "Juvenile osteochondrosis of marginal or vertebral ephiphysis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Scheuermann disease", "shortest_name_length": 5}
{"curie": "MONDO:0007259", "names": ["craniofaciofrontodigital syndrome", "Craniofaciofrontodigital syndrome", "CRANIOFACIOFRONTODIGITAL SYNDROME", "Craniofaciofrontodigital Syndrome", "Cantu craniofaciofrontodigital syndrome", "Cantu Craniofaciofrontodigital Syndrome", "CANTU CRANIOFACIOFRONTODIGITAL SYNDROME", "Craniofaciofrontodigital syndrome (disorder)", "craniofaciofrontodigital syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniofaciofrontodigital syndrome", "shortest_name_length": 33}
{"curie": "MONDO:0003443", "names": ["Papillary Urothelial Neoplasm", "papillary urothelial neoplasm", "urinary tract inverted papilloma", "inverted papilloma of urinary tract", "Inverted papilloma of urinary tract", "urothelium papillary epithelial neoplasm", "Urinary Tract Papillary Transitional Cell Neoplasm", "urinary tract papillary transitional cell neoplasm", "Papillary Transitional Cell Neoplasm of the Urinary Tract", "urinary tract papillary transitional cell benign neoplasm", "Papillary transitional cell neoplasm of the urinary tract", "papillary transitional cell neoplasm of the urinary tract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papillary urothelial neoplasm", "shortest_name_length": 29}
{"curie": "MONDO:0016464", "names": ["insulin resistance type B", "insulin-resistance type B", "insulin resistance, type B", "Insulin resistance - type B", "insulin-resistance syndrome type B", "Insulin-resistance syndrome type B", "Insulin resistance syndrome, type B", "insulin resistance, type B (diagnosis)", "Insulin resistance - type B (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "insulin-resistance syndrome type B", "shortest_name_length": 25}
{"curie": "MONDO:0001537", "names": ["TB epididymitis", "Epididymal tuberculosis", "epididymal tuberculosis", "Tuberculous epididymitis", "Epididymitis tuberculous", "tuberculous epididymitis", "tuberculosis of epididymis", "Tuberculosis of epididymis", "epididymis; tuberculous (etiology)", "tuberculosis; epididymis (etiology)", "epididymitis; tuberculous (etiology)", "tuberculous epididymitis (diagnosis)", "Tuberculosis of epididymis (disorder)", "epididymis; tuberculous (manifestation)", "Mycobacterium tuberculosis epididymitis", "tuberculosis; epididymis (manifestation)", "epididymitis; tuberculous (manifestation)", "tuberculosis; epididymitis (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tuberculous epididymitis", "shortest_name_length": 15}
{"curie": "MONDO:0034099", "names": ["SYNGAP1-related developmental and epileptic encephalopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SYNGAP1-related developmental and epileptic encephalopathy", "shortest_name_length": 58}
{"curie": "MONDO:0018927", "names": ["SUNCT headache", "SUNCT syndrome", "SUNCT Syndrome", "Syndrome, SUNCT", "SUNCT Syndromes", "Syndromes, SUNCT", "Short-lasting unilateral neuralgiform headache attacks with conjunctival injection and tearing", "short-lasting unilateral neuralgiform headache attacks with conjunctival injection and tearing", "Short-lasting Unilateral Neuralgiform Headache with Conjunctival Injection and Tearing Syndrome", "short-lasting, unilateral, neuralgiform headache attacks with conjunctival injection and tearing", "Short-lasting unilateral neuralgiform headache attacks with conjunctival injection and tearing syndrome", "SUNCT (short-lasting unilateral neuralgiform headache attacks with conjunctival injection and tearing) syndrome", "Short-lasting unilateral neuralgiform headache attacks with conjunctival injection and tearing syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SUNCT syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0017900", "names": ["MSMD due to complete IFNgammaR2 deficiency", "MSMD due to complete interferon gamma receptor 2 deficiency", "Mendelian susceptibility to mycobacterial diseases due to complete interferon gamma receptor 2 deficiency", "IFNGR2 autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency", "autosomal recessive Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency", "autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency caused by mutation in IFNGR2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency", "shortest_name_length": 42}
{"curie": "MONDO:0007055", "names": ["ACMICD", "acromicric dysplasia", "ACROMICRIC DYSPLASIA", "Acromicric dysplasia", "Acromicric Dysplasia", "acromicric skeletal dysplasia", "Acromicric skeletal dysplasia", "Acromicric dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acromicric dysplasia", "shortest_name_length": 6}
{"curie": "MONDO:0013661", "names": ["CMAMMA", "Cmamma", "Combined malonic and methylmalonic aciduria", "combined malonic and methylmalonic acidemia", "combined malonic and methylmalonic aciduria", "Combined malonic and methylmalonic acidemia", "COMBINED MALONIC AND METHYLMALONIC ACIDURIA", "Combined Malonic and Methylmalonic Aciduria", "CMAMMA - combined malonic and methylmalonic aciduria", "Combined malonic and methylmalonic aciduria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined malonic and methylmalonic acidemia", "shortest_name_length": 6}
{"curie": "MONDO:0001298", "names": ["mr", "mrs", "Incompetence;mitral", "Mitral incompetence", "Mitral Incompetence", "mitral incompetence", "mitral insufficiency", "Mitral regurgitation", "Mitral Insufficiency", "Incompetence, Mitral", "Mitral insufficiency", "MITRAL INSUFFICIENCY", "Mitral Regurgitation", "MITRAL REGURGITATION", "mitral regurgitation", "mitral; insufficiency", "insufficiency; mitral", "Regurgitation, Mitral", "mitral regurgitations", "insufficiency, mitral", "Insufficiency, Mitral", "MI - Mitral incompetence", "Mild mitral regurgitation", "MITRAL VALVE INCOMPETENCE", "MR - Mitral regurgitation", "mitral regurgitation (MR)", "mitral valve incompetence", "Mitral Valve Incompetence", "Mitral regurgitation, NOS", "Mitral valve incompetence", "Mitral regurgitation, mild", "MITRAL VALVE, INCOMPETENCY", "MITRAL VALVE REGURGITATION", "Mitral Valve Regurgitation", "Mitral Valve Insufficiency", "mitral valve insufficiency", "mitral valve regurgitation", "Mitral valve regurgitation", "Incompetence, Mitral Valve", "Valve Incompetence, Mitral", "Mitral valve insufficiency", "MITRAL VALVE INSUFFICIENCY", "Regurgitation, Mitral Valve", "Insufficiency, Mitral Valve", "Valve Insufficiency, Mitral", "Valve Regurgitation, Mitral", "Mitral (valve) insufficiency", "Insufficiency of mitral valve", "Mitral valve incompetence, NOS", "Mitral and aortic incompetence", "congenital mitral insufficiency", "congenital insufficiency mitral", "Mitral valve regurgitation, NOS", "congenital mitral regurgitation", "Mitral valve insufficiency, NOS", "Congenital mitral regurgitation", "Congenital mitral insufficiency", "Mitral and aortic insufficiency", "Mitral and aortic regurgitation", "mitral regurgitation (diagnosis)", "Mitral regurgitation, congenital", "insufficiency; mitral, congenital", "regurgitation; mitral, congenital", "atrioventricular regurgitation left", "Congenital mitral valve incompetence", "MR - Congenital mitral regurgitation", "Mitral and aortic valve regurgitation", "Mitral valve regurgitation (disorder)", "congenital mitral valve insufficiency", "Congenital insufficiency of mitral valve", "congenital insufficiency of mitral valve", "Mitral and aortic incompetence (disorder)", "Left atrioventricular valve regurgitation", "Mitral Valve Insufficiency/ Regurgitation", "congenital mitral regurgitation (diagnosis)", "Regurgitation of left atrioventricular valve", "insufficiency of mitral valve and aortic valve", "Congenital insufficiency of mitral valve (disorder)", "Left atrioventricular valve regurgitation (diagnosis)", "Mitral valve insufficiency and aortic valve insufficiency", "insufficiency of mitral valve and aortic valve (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital mitral valve insufficiency", "shortest_name_length": 2}
{"curie": "MONDO:0033202", "names": ["DFNB109", "autosomal recessive deafness 109", "DEAFNESS, AUTOSOMAL RECESSIVE 109", "deafness, autosomal recessive 109", "hearing loss, autosomal recessive 109", "autosomal recessive nonsyndromic deafness 109"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal recessive 109", "shortest_name_length": 7}
{"curie": "MONDO:0006563", "names": ["Inverted keratosis", "Inverted folicular keratosis", "inverted folicular keratosis", "Keratosis punctata acquisita", "inverted follicular keratosis", "Inverted follicular keratosis", "Inverted Follicular Keratosis", "Inverted follicular keratosis (disorder)", "Inverted keratosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inverted follicular keratosis", "shortest_name_length": 18}
{"curie": "MONDO:0005758", "names": ["eunuchism", "Eunuchism", "eunuchoidism", "EUNUCHOIDISM", "Eunuchoidism", "Eunuchoidism NOS", "Hypogonadism male", "HYPOGONADISM MALE", "Eunuchoidism, NOS", "hypogonadism male", "male hypogonadism", "Male hypogonadism", "HYPOGONADISM, MALE", "Testicular Failure", "Testicular failure", "hypogonadism; male", "Hypogonadism, Male", "testicular failure", "failure testicular", "hypogonadism males", "Eunuchism (disorder)", "Testicular failure NOS", "Male hypogonadism, NOS", "Hypogonadism (in males)", "Testicular failure, NOS", "Testicular hypogonadism", "hypogonadism; testicular", "testicular; hypogonadism", "Eunuchoidism hypogonadism", "Primary Testicular Failure", "Eunuchoidism, hypogonadism", "Primary testicular failure", "Testicular hypogonadism NOS", "Male hypogonadism (disorder)", "Testicular hypogonadism, NOS", "hypogonadotropic eunuchoidism", "Hypogonadotropic eunuchoidism", "EUNUCHOIDISM, HYPOGONADOTROPIC", "hypogonadotropic; eunuchoidism", "testicular failure (diagnosis)", "eunuchoidism; hypogonadotropic", "Decreased function of male gonad", "Male hypergonadotropic hypogonadism", "Male Hypergonadotropic Hypogonadism", "hypergonadotropic hypogonadism (Male)", "Hypergonadotropic Hypogonadism (Male)", "Hypogonadotropic eunuchoidism syndrome", "hypogonadotropic eunuchoidism (diagnosis)", "Hypogonadotropic hypogonadism syndrome, male"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eunuchism", "shortest_name_length": 9}
{"curie": "UMLS:C0948300", "names": ["Application site scab", "Application site scabbing"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Application site scab", "shortest_name_length": 21}
{"curie": "MONDO:0015907", "names": ["epimetaphyseal skeletal dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epimetaphyseal skeletal dysplasia", "shortest_name_length": 33}
{"curie": "UMLS:C0521549", "names": ["Gastrointestinal Tract AVM/H", "Gastrointestinal Tract Arteriovenous Malformation", "Congenital arteriovenous anomaly of gastrointestinal tract", "Gastrointestinal Tract Arteriovenous Malformation/Hemangioma", "Arteriovenous malformation of the gastrointestinal tract, NOS", "Congenital arteriovenous malformation of gastrointestinal tract", "Congenital arteriovenous malformation of gastrointestinal tract (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital arteriovenous malformation of gastrointestinal tract", "shortest_name_length": 28}
{"curie": "MONDO:0020058", "names": ["Allosome anomaly", "gonosome anomaly", "Sex-chromosome anomaly", "anomalies chromosome sex", "sex chromosomes; anomaly", "Anomaly of sex chromosome", "anomaly of sex chromosome", "chromosome; abnormal, sex", "Sex Chromosome Aberration", "Chromosome Aberration, Sex", "sex chromosome abnormality", "Aberration, Sex Chromosome", "Sex Chromosome Abnormality", "Sex Chromosome Aberrations", "Sex chromosome abnormality", "Aberrations, Sex Chromosome", "Chromosome Abnormality, Sex", "Abnormality, Sex Chromosome", "Chromosome Aberrations, Sex", "Sex Chromosome Abnormalities", "sex chromosome abnormalities", "Sex chromosome abnormalities", "Sex chromosomal abnormalities", "sex chromosomal abnormalities", "Abnormalities, Sex Chromosome", "Chromosome Abnormalities, Sex", "Anomaly of sex chromosome, NOS", "Sex chromosome abnormality NOS", "abnormal; chromosome, sex chromosome", "Anomaly of sex chromosome (disorder)", "anomaly of sex chromosome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gonosome anomaly", "shortest_name_length": 16}
{"curie": "MONDO:0005490", "names": ["large artery stroke"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "large artery stroke", "shortest_name_length": 19}
{"curie": "MONDO:0013614", "names": ["HPPD", "hypertelorism, preauricular sinus, punctal pits, and deafness", "HYPERTELORISM, PREAURICULAR SINUS, PUNCTAL PITS, AND DEAFNESS", "hypertelorism-preauricular sinus-punctual pits-deafness syndrome", "Hypertelorism-preauricular sinus-punctual pits-deafness syndrome", "Hypertelorism, preauricular sinus, punctual pits, deafness syndrome", "Hypertelorism-preauricular sinus-punctual pits-hearing loss syndrome", "hypertelorism-preauricular sinus-punctual pits-hearing loss syndrome", "Hypertelorism, preauricular sinus, punctual pits, hearing loss syndrome", "HPPD (hypertelorism, preauricular sinus, punctual pits, deafness) syndrome", "Hypertelorism, preauricular sinus, punctual pits, deafness syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertelorism-preauricular sinus-punctual pits-deafness syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0852709", "names": ["Leukemic lymphoma", "Leukemic Lymphoma", "Leukaemic lymphoma", "Leukemic Phase of Lymphoma", "Leukemic Phase of Non-Hodgkin Lymphoma", "Leukemic Phase of Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leukemic Phase of Non-Hodgkin's Lymphoma", "shortest_name_length": 17}
{"curie": "UMLS:C4049615", "names": ["Megaureter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Megaureter", "shortest_name_length": 10}
{"curie": "UMLS:C0854996", "names": ["Relapsed Pharynx Cancer", "Recurrent Pharynx Cancer", "Relapsed Pharynx Carcinoma", "Relapsed Cancer of Pharynx", "Relapsed Pharyngeal Cancer", "Recurrent Cancer of Pharynx", "Pharyngeal cancer recurrent", "Recurrent Pharyngeal Cancer", "Recurrent Pharynx Carcinoma", "Pharyngeal Cancer, Recurrent", "Relapsed Carcinoma of Pharynx", "Relapsed Pharyngeal Carcinoma", "Relapsed Cancer of the Pharynx", "Recurrent Pharyngeal Carcinoma", "Recurrent Carcinoma of Pharynx", "Recurrent Cancer of the Pharynx", "Relapsed Carcinoma of the Pharynx", "Recurrent Pharyngeal Throat Cancer", "Recurrent Carcinoma of the Pharynx"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pharyngeal cancer recurrent", "shortest_name_length": 23}
{"curie": "MONDO:0009724", "names": ["NPLRD", "FSGS10", "Salcedo syndrome", "Nail patella-like renal disease", "Nail-Patella-Like Renal Disease", "nail patella like renal disease", "Nail-patella-like renal disease", "nail-patella-like renal disease", "Nail patella like renal disease", "NAIL-PATELLA-LIKE RENAL DISEASE", "focal segmental glomerulosclerosis 10", "FOCAL SEGMENTAL GLOMERULOSCLEROSIS 10", "GLOMERULOSCLEROSIS, FOCAL SEGMENTAL, 10", "Nail patella-like renal disease (disorder)", "GLOMERULAR BASEMENT MEMBRANE DISEASE, NAIL-PATELLA SYNDROME TYPE", "Glomerular basement membrane disease, nail-patella syndrome type", "glomerular basement Membrane disease, nail-patella syndrome type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nail-patella-like renal disease", "shortest_name_length": 5}
{"curie": "UMLS:C5557379", "names": ["Vulvar Kaposi Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Kaposi Sarcoma", "shortest_name_length": 21}
{"curie": "MONDO:0025510", "names": ["Pythiosis", "pythiosis", "Pythioses", "swamp cancer", "Swamp cancer", "human pythiosis", "Pythiosis Insidiosi", "Equine dermal granuloma", "Hyphomycosis destruens equi", "pythium insidiosum infection", "Pythium insidiosum Infection", "Pythium insidiosum infection", "Infection, Pythium insidiosum", "Pythium insidiosum Infections", "Infection by Pythium insidiosum", "Infection by Hyphomyces destruens"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pythiosis", "shortest_name_length": 9}
{"curie": "UMLS:C0280170", "names": ["Stage IV Grade 2 Follicular Lymphoma", "stage IV grade 2 follicular lymphoma", "Grade II Follicular Lymphoma Stage IV", "Stage IV Grade II Follicular Lymphoma", "Metastatic Grade II Follicular Lymphoma", "Stage IV Follicular Mixed Cell Lymphoma", "Follicular Mixed Cell Lymphoma Stage IV", "follicular mixed cell lymphoma, stage IV", "metastatic follicular mixed cell lymphoma", "follicular mixed cell lymphoma, metastatic", "Ann Arbor Stage IV Grade 2 Follicular Lymphoma", "Grade II Follicular Mixed Cell Lymphoma Stage IV", "stage IV grade II follicular mixed cell lymphoma", "Stage IV Grade II Follicular Mixed Cell Lymphoma", "Metastatic Grade II Follicular Mixed Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage IV Grade 2 Follicular Lymphoma", "shortest_name_length": 36}
{"curie": "MONDO:0009772", "names": ["ORC syndrome", "ORC SYNDROME", "Oculorenocerebellar syndrome", "oculorenocerebellar syndrome", "OCULORENOCEREBELLAR SYNDROME", "Hunter-Jurenka-Thompson syndrome", "Hunter Jurenka Thompson syndrome", "ORC (oculo-renal-cerebellar) syndrome", "Severe oculo-renal-cerebellar syndrome", "Severe oculo-renal-cerebellar syndrome (disorder)", "absence of the cerebellar granular layer, mental retardation, tapetoretinal degeneration and progressive glomerulopathy", "absence of the cerebellar granular layer, intellectual disability, tapetoretinal degeneration and progressive glomerulopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculorenocerebellar syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0013495", "names": ["ARCI8", "LI4, FORMERLY", "lamellar ichthyosis 4", "ichthyosis, lamellar, 4", "late-onset lamellar ichthyosis", "lamellar ichthyosis, late-onset", "LAMELLAR ICHTHYOSIS, LATE-ONSET", "ICHTHYOSIS, LAMELLAR, 4, FORMERLY", "ichthyosis, lamellar, 4, formerly", "autosomal recessive congenital ichthyosis 8", "ichthyosis, congenital, autosomal recessive 8", "ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 8", "autosomal recessive congenital ichthyosis type 8", "ichthyosis, congenital, autosomal recessive type 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive congenital ichthyosis 8", "shortest_name_length": 5}
{"curie": "UMLS:C0457532", "names": ["Granular cell ameloblastoma", "Granular Cell Ameloblastoma", "Granular cell ameloblastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Granular cell ameloblastoma", "shortest_name_length": 27}
{"curie": "MONDO:0018876", "names": ["MCL", "LCM", "DPDL lymphoma", "cell lymphoma mantle", "mantle zone lymphoma", "Mantle-Cell Lymphoma", "mantle cell lymphoma", "MANTLE CELL LYMPHOMA", "Mantle-Zone Lymphoma", "mantle-cell lymphoma", "diffuse PDL lymphoma", "Mantle Zone Lymphoma", "Mantle zone lymphoma", "Mantle Cell Lymphoma", "Mantle cell lymphoma", "Lymphoma, Mantle-Cell", "Mantle-Cell Lymphomas", "lymphoma; mantle zone", "Lymphoma, Mantle-Zone", "Mantle cell lymphomas", "Mantle-Zone Lymphomas", "mantle cell lymphomas", "Lymphoma, Mantle Cell", "mantle zone; lymphoma", "lymphoma, mantle cell", "Lymphomas, Mantle-Cell", "Lymphomas, Mantle-Zone", "Mantle cell lymphoma NOS", "Classical Mantle Cell Lymphoma", "classical mantle cell lymphoma", "Multiple Lymphomatous Polyposis", "Mantle cell lymphoma (disorder)", "Centrocytic Small-Cell Lymphoma", "Malignant lymphomatous polyposis", "Lymphoma, Centrocytic Small-Cell", "Lymphoma, Centrocytic Small Cell", "Centrocytic Small-Cell Lymphomas", "mantle cell lymphoma (diagnosis)", "Small-Cell Lymphoma, Centrocytic", "Multifocal Lymphomatous Polyposis", "Lymphomas, Centrocytic Small-Cell", "Small-Cell Lymphomas, Centrocytic", "Lymphoma, Small-Cell, Centrocytic", "Mantle cell lymphoma (morphologic abnormality)", "diffuse poorly-differentiated lymphocytic lymphoma", "Diffuse Lymphocytic Lymphoma, Poorly Differentiated", "Diffuse Lymphocytic Lymphoma, Poorly-Differentiated", "Lymphocytic Lymphoma, Diffuse, Poorly-Differentiated", "Lymphocytic lymphoma, poorly differentiated, diffuse", "Lymphocytic Lymphoma, Diffuse, Poorly Differentiated", "Lymphoma, Lymphocytic, Diffuse, Poorly-Differentiated", "lymphoma; diffuse, lymphocytic, poorly differentiated", "diffuse; lymphoma, lymphocytic, poorly differentiated", "Lymphocytic lymphosarcoma, intermediate differentiation", "Lymphoma, Lymphocytic, Diffuse, Intermediate Differentiated", "Malignant lymphoma, lymphocytic, poorly differentiated, diffuse", "Lymphocytic lymphosarcoma, intermediate differentiation, diffuse", "Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mantle cell lymphoma", "shortest_name_length": 3}
{"curie": "MONDO:0018591", "names": ["AMYLOIDOSIS VI", "Amyloidosis VI", "Amyloidosis VIs", "ACys amyloidosis", "ITM2B amyloidosis", "Cystatin amyloidosis", "HCHWA, Icelandic type", "CST3-related amyloidosis", "Iceland type amyloidosis", "ITM2B-related amyloidosis", "Icelandic type amyloidosis", "Icelandic Type Amyloidosis", "Amyloidosis, Icelandic Type", "familial cerebral amyloid angiopathy", "Hereditary cystatin C amyloid angiopathy", "Cerebral Amyloid Angiopathy, Cst3-Related", "Cerebral Amyloid Angiopathy, Cst3 Related", "ITM2B-related cerebral amyloid angiopathy", "CEREBRAL AMYLOID ANGIOPATHY, CST3-RELATED", "AMYLOIDOSIS, CEREBROARTERIAL, ICELANDIC TYPE", "Amyloidosis, Cerebroarterial, Icelandic Type", "Icelandic Type Hereditary Cerebral Amyloid Angiopathy", "Hereditary Cerebral Amyloid Angiopathy, Icelandic Type", "Hereditary cerebral amyloid angiopathy, Icelandic type", "Hereditary cerebral hemorrhage with amyloidosis, Icelandic type", "Hereditary cerebral hemorrhage with amyloidosis - Icelandic type", "Hereditary cerebral haemorrhage with amyloidosis - Icelandic type", "Hereditary cerebral amyloid angiopathy, Icelandic type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ITM2B amyloidosis", "shortest_name_length": 14}
{"curie": "MONDO:0023176", "names": ["Formalin Toxicity", "Formalin toxicity", "Formalin Intoxication", "Formalin intoxication", "formaldehyde exposure", "formaldehyde toxicity", "Formaldehyde Toxicity", "Formaldehyde Exposure", "formaldehyde poisoning", "Formaldehyde poisoning", "FORMALDEHYDE POISONING", "poisoning by formaldehyde", "Toxic effect of formaldehyde", "Toxic effect of formaldehyde NOS", "poisoning by formaldehyde (diagnosis)", "Toxic effect of formaldehyde (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "formaldehyde poisoning", "shortest_name_length": 17}
{"curie": "UMLS:C0278827", "names": ["Relapsed Bladder Cancer", "Recurrent Bladder Cancer", "Bladder cancer recurrent", "recurrent bladder cancer", "bladder cancer, recurrent", "Bladder Cancer, Recurrent", "Relapsed Cancer of Bladder", "Bladder Carcinoma Recurrent", "Bladder carcinoma recurrent", "Carcinoma bladder recurrent", "Recurrent Bladder Carcinoma", "Recurrent Cancer of Bladder", "Relapsed Cancer of the Bladder", "recurrent cancer of the bladder", "Recurrent Cancer of the Bladder", "Relapsed Urinary Bladder Cancer", "cancer of the bladder, recurrent", "Recurrent Urinary Bladder Cancer", "Relapsed Cancer of Urinary Bladder", "recurrent carcinoma of the bladder", "carcinoma of the bladder, recurrent", "Recurrent Cancer of Urinary Bladder", "Carcinoma urinary bladder recurrent", "Urinary bladder carcinoma recurrent", "Relapsed Cancer of the Urinary Bladder", "Recurrent Cancer of the Urinary Bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder cancer recurrent", "shortest_name_length": 23}
{"curie": "MONDO:0001384", "names": ["myopia", "Myopic", "Myopia", "MYOPIA", "Myopias", "near sight", "near vision", "nearsighted", "short sight", "Nearsighted", "near sighted", "Near sighted", "short sighted", "Close sighted", "Short-sighted", "short-sighted", "Nearsightedness", "disorder myopia", "obsolete_myopia", "nearsightedness", "Near sightedness", "myopia (disease)", "near-sightedness", "Near-sightedness", "near sightedness", "Myopia (disorder)", "Short sightedness", "short-sightedness", "short sightedness", "SHORT SIGHTEDNESS", "Nearsightednesses", "shortness of sight", "myopia (diagnosis)", "Shortness (of);sight"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopia", "shortest_name_length": 6}
{"curie": "MONDO:0015553", "names": ["DEB-na", "nails-only DEB", "nails-only DDEB", "Localized DEB, nails only", "Dystrophic epidermolysis bullosa nails only", "dystrophic epidermolysis bullosa, nails only", "Nails only DEB (dystrophic epidermolysis bullosa)", "dominant dystrophic epidermolysis bullosa, nails only", "Localized dystrophic epidermolysis bullosa, nails only", "Dystrophic epidermolysis bullosa nails only (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dystrophic epidermolysis bullosa, nails only", "shortest_name_length": 6}
{"curie": "UMLS:C0003044", "names": ["Bite;animal", "animal bite", "Animal bite", "ANIMAL BITE", "animal bites", "animal; bite", "Animal Bites", "bite; animal", "animals bites", "Animal bite NOS", "Bite by unspecified animal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Animal bite", "shortest_name_length": 11}
{"curie": "MONDO:0010065", "names": ["SDSEM", "spinocerebellar degeneration with slow eye movements"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar degeneration with slow eye movements", "shortest_name_length": 5}
{"curie": "MONDO:0007066", "names": ["adenosine triphosphatase deficiency anemia", "anemia due to adenosine triphosphatase deficiency", "Anemia due to adenosine triphosphatase deficiency", "adenosine triphosphatase deficiency, anemia due to", "Adenosine Triphosphatase Deficiency, Anemia Due To", "ADENOSINE TRIPHOSPHATASE DEFICIENCY, ANEMIA DUE TO", "Anaemia due to adenosine triphosphatase deficiency", "Nonspherocytic hemolytic anemia due to deficiency of adenosinetriphosphatase", "Nonspherocytic haemolytic anaemia due to deficiency of adenosinetriphosphatase", "Nonspherocytic hemolytic anemia due to deficiency of adenosinetriphosphatase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenosine triphosphatase deficiency, anemia due to", "shortest_name_length": 42}
{"curie": "UMLS:C1336755", "names": ["Thyroid Non-Hodgkin Lymphoma", "Thyroid Non-Hodgkin's Lymphoma", "Non-Hodgkin's Lymphoma of Thyroid", "Thyroid Gland Non-Hodgkin Lymphoma", "Thyroid Gland Non-Hodgkin's Lymphoma", "Non-Hodgkin's Lymphoma of the Thyroid", "Non-Hodgkin's Lymphoma of Thyroid Gland", "non-Hodgkin's lymphoma of thyroid gland", "Non-Hodgkin's Lymphoma of the Thyroid Gland", "Primary Thyroid Gland Non-Hodgkin's Lymphoma", "non-Hodgkin's lymphoma of thyroid gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Non-Hodgkin's Lymphoma", "shortest_name_length": 28}
{"curie": "MONDO:0021192", "names": ["odontogenic tumor", "Odontogenic tumor", "Odontogenic Tumor", "Odontogenic tumour", "odontogenic tumors", "tumor; odontogenic", "odontogenic tumour", "Tumor, Odontogenic", "ODONTOGENIC TUMORS", "Odontogenic Tumors", "Odontogenic tumors", "odontogenic; tumor", "Tumors, Odontogenic", "odontogenic neoplasm", "Odontogenic Neoplasm", "Odontogenic neoplasm", "odontogenic neoplasms", "Odontogenic tumor NOS", "Odontogenic tumour NOS", "Odontogenic tumor, NOS", "calcareous tooth tumor", "Odontogenic tumour, NOS", "tumor of calcareous tooth", "calcareous tooth neoplasm", "neoplasm of calcareous tooth", "Odontogenic neoplasm (morphology)", "odontogenic neoplasms (diagnosis)", "calcareous tooth neoplasm (disease)", "Odontogenic neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "odontogenic neoplasm", "shortest_name_length": 17}
{"curie": "MONDO:0008276", "names": ["jPS", "juvenile polyposis coli", "juvenile polyposis syndrome", "juvenile intestinal polyposis", "juvenile polyposis of stomach", "polyposis, juvenile intestinal", "polyposis, familial, of Entire gastrointestinal tract", "generalized juvenile polyposis/juvenile polyposis coli"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "generalized juvenile polyposis/juvenile polyposis coli", "shortest_name_length": 3}
{"curie": "MONDO:0015408", "names": ["Gla", "GLA", "diffuse lymphangioma", "Diffuse lymphangioma", "Diffuse lymphangiomatosis", "diffuse lymphangiomatosis", "disseminated lymphangioma", "Disseminated lymphangioma", "generalized lymphatic anomaly", "Generalized lymphatic anomaly", "Disseminated lymphangiomatosis", "Diffuse lymphatic malformation", "disseminated lymphangiomatosis", "diffuse lymphatic malformation", "Diffuse lymphangioma (disorder)", "Disseminated lymphatic malformation", "disseminated lymphatic malformation", "Diffuse lymphatic malformation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diffuse lymphatic malformation", "shortest_name_length": 3}
{"curie": "MONDO:0024618", "names": ["poliovirus infection", "human poliovirus infection", "Human poliovirus infection", "Enterovirus C infectious disease", "Enterovirus C disease or disorder", "infection caused by human poliovirus", "Infection caused by Human poliovirus", "Enterovirus C caused disease or disorder", "Infection caused by Human poliovirus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "poliovirus infection", "shortest_name_length": 20}
{"curie": "MONDO:0001066", "names": ["late yaws", "Late Yaws", "Yaws gumma", "Yaws ulcer", "gumma; yaws", "yaws; ulcer", "ulcer; yaws", "yaws; gumma", "ulcers; yaws", "yaws; ulcers", "Ulcers of yaws", "gummatous yaws", "ulcers of yaws", "gummata of yaws", "Gummata of yaws", "Nodular late yaws", "nodular late yaws", "ulcers due to yaws", "yaws; late nodular", "late nodular; yaws", "gummatous frambeside", "Gummatous frambeside", "gummatous; frambeside", "Gummatous framboeside", "frambeside; gummatous", "yaws gummata and ulcers", "Yaws gummata and ulcers", "Gummata and ulcers of yaws", "gummatous yaws (diagnosis)", "Nodular late yaws (disorder)", "gumma; ulcerative due to yaws", "gummata and ulcers due to yaws", "Gummata and ulcers due to yaws", "ulcers due to yaws (diagnosis)", "Yaws gummata and ulcers (disorder)", "Multiple papillomata and wet crab yaws", "Multiple papillomata due to yaws and wet crab yaws", "multiple papillomata due to yaws and wet crab yaws"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "late yaws", "shortest_name_length": 9}
{"curie": "UMLS:C2350988", "names": ["Proliferative Bronchiolitis", "Bronchiolitis, Proliferative", "Proliferative Bronchiolitides", "Bronchiolitides, Proliferative"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bronchiolitis, Proliferative", "shortest_name_length": 27}
{"curie": "MONDO:0044318", "names": ["JDVS", "IDDGIP", "IDDGIP, FORMERLY", "Jansen de Vries syndrome", "JANSEN-DE VRIES SYNDROME", "intellectual developmental disorder with gastrointestinal difficulties and high pain threshold", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD, FORMERLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder with gastrointestinal difficulties and high pain threshold", "shortest_name_length": 4}
{"curie": "UMLS:C5204068", "names": ["Locally Advanced Large Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Large Cell Neuroendocrine Carcinoma", "shortest_name_length": 52}
{"curie": "UMLS:C5206696", "names": ["Locally Advanced Bladder Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Bladder Urothelial Carcinoma", "shortest_name_length": 45}
{"curie": "UMLS:C5206186", "names": ["Esophageal Intramucosal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Intramucosal Adenocarcinoma", "shortest_name_length": 38}
{"curie": "UMLS:C5204120", "names": ["Type I Cryoglobulinemic Glomerulonephritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Type I Cryoglobulinemic Glomerulonephritis", "shortest_name_length": 42}
{"curie": "MONDO:0019072", "names": ["ricp", "RICP", "Obstetric Cholestasis", "pregnancy cholestasis", "cholestasis pregnancy", "cholestasis intrahepatic", "cholestasis of pregnancy", "Intrahepatic Cholestasis", "Intrahepatic cholestasis", "CHOLESTASIS OF PREGNANCY", "intrahepatic cholestasis", "Intrahepatic Cholestases", "Cholestasis intrahepatic", "Cholestasis of pregnancy", "CHOLESTASIS INTRAHEPATIC", "Cholestasis, Intrahepatic", "Cholestases, Intrahepatic", "Intrahepatic Biliary Stases", "Intrahepatic Biliary Stasis", "Biliary Stasis, Intrahepatic", "Biliary Stases, Intrahepatic", "Pregnancy-Related Cholestasis", "Pregnancy related cholestasis", "Pregnancy-related cholestasis", "Cholestasis, Pregnancy-Related", "recurrent jaundice of pregnancy", "Recurrent jaundice of pregnancy", "neonatal intrahepatic cholestasis", "Gravidic intrahepatic cholestasis", "Intrahepatic cholestasis (finding)", "Impaired release of bile from liver", "Cholestasis of pregnancy (disorder)", "Bile Duct Obstruction, Intrahepatic", "Intrahepatic cholestasis of pregnancy", "Intrahepatic Cholestasis of Pregnancy", "Cholestasis, intrahepatic of pregnancy", "Cholestasis, Intrahepatic, Of Pregnancy", "recurrent jaundice of pregnancy (diagnosis)", "Recurrent intrahepatic cholestasis of pregnancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intrahepatic cholestasis", "shortest_name_length": 4}
{"curie": "UMLS:C1112488", "names": ["Neonatal bradycardia", "neonatal bradycardia", "Bradycardia neonatal", "Neonatal bradycardia (disorder)", "neonatal bradycardia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neonatal bradycardia", "shortest_name_length": 20}
{"curie": "MONDO:0001874", "names": ["ototoxicity", "Ototoxicity", "OTOTOXICITY", "Ototoxicities", "Ototoxicity, NOS", "toxic labyrinthitis", "Toxic labyrinthitis", "labyrinthitis toxic", "Ototoxicity (disorder)", "Toxic labyrinthitis (disorder)", "toxic labyrinthitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "toxic labyrinthitis", "shortest_name_length": 11}
{"curie": "UMLS:C3248383", "names": ["Logorrhea", "Logomania", "POLYLOGIA", "logorrhea", "Logorrhoea", "LOGORRHOEA", "Logorrhea (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Logorrhea", "shortest_name_length": 9}
{"curie": "UMLS:C1710110", "names": ["Small Intestinal Signet Ring Cell Carcinoma", "Small Intestinal Signet-Ring Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Intestinal Signet Ring Cell Carcinoma", "shortest_name_length": 43}
{"curie": "UMLS:C0855201", "names": ["Stage II Supradiaphragmatic Mixed Cellularity Hodgkin Lymphoma", "Hodgkin's disease mixed cellularity stage II supradiaphragmatic", "Stage II Supradiaphragmatic Mixed Cellularity Hodgkin's Disease", "Stage II Supradiaphragmatic Mixed Cellularity Hodgkin's Lymphoma", "Stage II Mixed Cellularity Hodgkin's Disease above the Diaphragm", "Stage II Mixed Cellularity Hodgkin's Lymphoma above the Diaphragm", "Stage II Supradiaphragmatic Mixed Cellularity Classical Hodgkin Lymphoma", "Ann Arbor Stage II Supradiaphragmatic Mixed Cellularity Classic Hodgkin Lymphoma", "Ann Arbor Stage II Supradiaphragmatic Mixed Cellularity Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's disease mixed cellularity stage II supradiaphragmatic", "shortest_name_length": 62}
{"curie": "MONDO:0006855", "names": ["Mesenteric Vascular Occlusion", "mesenteric vascular occlusion", "Mesenteric vascular occlusion", "Vascular Occlusion, Mesenteric", "Mesenteric Vascular Occlusions", "Occlusion, Mesenteric Vascular", "Vascular Occlusions, Mesenteric", "Occlusions, Mesenteric Vascular"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mesenteric vascular occlusion", "shortest_name_length": 29}
{"curie": "MONDO:0017103", "names": ["encephaloclastic disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephaloclastic disorder", "shortest_name_length": 25}
{"curie": "MONDO:0010725", "names": ["RS", "RS1", "XJR", "XLRS", "XLRS1", "X-Linked Retinoschises", "Juvenile Retinoschises", "x-linked retinoschisis", "Juvenile retinoschisis", "x linked retinoschisis", "X-Linked Retinoschisis", "Juvenile Retinoschisis", "X Linked Retinoschisis", "retinoschisis X-linked", "X-linked retinoschisis", "juvenile retinoschisis", "Retinoschisis, Juvenile", "retinoschisis, X-linked", "Retinoschises, Juvenile", "Retinoschisis, X Linked", "Retinoschises, X-Linked", "Retinoschisis, X-Linked", "X-Linked Juvenile Retinoschises", "x-linked juvenile retinoschisis", "juvenile X-linked retinoschisis", "X Linked Juvenile Retinoschisis", "juvenile x-linked retinoschisis", "X-Linked Juvenile Retinoschisis", "X-linked juvenile retinoschisis", "Retinoschisis X-Linked Juvenile", "Juvenile X-Linked Retinoschisis", "Retinoschises, X-Linked Juvenile", "Juvenile Retinoschises, X-Linked", "Retinoschisis, X-Linked Juvenile", "Juvenile Retinoschisis, X-Linked", "Juvenile retinoschisis (disorder)", "Congenital X Linked Retinoschisis", "Congenital X-Linked Retinoschisis", "retinoschisis, X-linked recessive", "Congenital X-Linked Retinoschises", "X-linked juvenile retinoschisis 1", "Retinoschisis, Juvenile, X-Linked", "X-Linked Retinoschises, Congenital", "Retinoschisis, Congenital X-Linked", "Retinoschises, Congenital X-Linked", "X-Linked Retinoschisis, Congenital", "juvenile retinoschisis (diagnosis)", "retinoschisis 1, X-linked, juvenile", "RETINOSCHISIS 1, X-LINKED, JUVENILE", "X-linked juvenile retinoschisis type 1", "retinoschisis juvenile X chromosome-linked", "Retinoschisis, Juvenile, X Chromosome-Linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked retinoschisis", "shortest_name_length": 2}
{"curie": "MONDO:0004370", "names": ["Sphenocavernous Meningioma", "sphenocavernous meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sphenocavernous meningioma", "shortest_name_length": 26}
{"curie": "UMLS:C0280376", "names": ["Relapsed Oropharyngeal SCC", "Relapsed SCC of Oropharynx", "Recurrent Oropharyngeal SCC", "Recurrent SCC of Oropharynx", "Relapsed SCC of the Oropharynx", "Recurrent SCC of the Oropharynx", "Relapsed Oropharyngeal Epidermoid Carcinoma", "Relapsed Epidermoid Carcinoma of Oropharynx", "Recurrent Oropharyngeal Epidermoid Carcinoma", "Recurrent Epidermoid Carcinoma of Oropharynx", "oropharynx squamous cell carcinoma, recurrent", "Relapsed Oropharyngeal Squamous Cell Carcinoma", "Relapsed Squamous Cell Carcinoma of Oropharynx", "Recurrent Oropharyngeal Squamous Cell Carcinoma", "Recurrent Squamous Cell Carcinoma of Oropharynx", "Relapsed Epidermoid Carcinoma of the Oropharynx", "Oropharyngeal squamous cell carcinoma recurrent", "Recurrent Epidermoid Carcinoma of the Oropharynx", "oropharyngeal squamous cell carcinoma, recurrent", "epidermoid carcinoma of the oropharynx, recurrent", "Relapsed Squamous Cell Carcinoma of the Oropharynx", "Recurrent Squamous Cell Carcinoma of the Oropharynx", "recurrent squamous cell carcinoma of the oropharynx", "Recurrent Oropharyngeal Throat Squamous Cell Cancer", "squamous cell carcinoma of the oropharynx, recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oropharyngeal squamous cell carcinoma recurrent", "shortest_name_length": 26}
{"curie": "UMLS:C0278852", "names": ["Stage I Thyroid Follicular Cancer", "stage I follicular thyroid cancer", "thyroid cancer, stage I follicular", "follicular thyroid cancer, stage I", "Stage I Thyroid Follicular Carcinoma", "Stage I Thyroid Gland Follicular Cancer", "Stage I Follicular Carcinoma of Thyroid", "carcinoma, follicular, thyroid, stage I", "Stage I Thyroid Gland Follicular Carcinoma", "Stage I Follicular Thyroid Gland Carcinoma", "Stage I Follicular Carcinoma of the Thyroid", "follicular carcinoma of the thyroid, stage I", "Stage I Follicular Carcinoma of Thyroid Gland", "Stage I Follicular Carcinoma of the Thyroid Gland", "Stage I Thyroid Gland Follicular Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Thyroid Gland Follicular Carcinoma AJCC v7", "shortest_name_length": 33}
{"curie": "UMLS:C4527068", "names": ["Pathologic Stage II Merkel Cell Carcinoma AJCC v8", "Pathologic Stage II Neuroendocrine Carcinoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage II Merkel Cell Carcinoma AJCC v8", "shortest_name_length": 49}
{"curie": "UMLS:C0748023", "names": ["PROSTATITIS SEPTIC", "prostatitis bacterial", "Bacterial Prostatitis", "bacterial prostatitis", "PROSTATITIS BACTERIAL", "Bacterial prostatitis", "Prostatitis caused by bacteria", "Bacterial prostatitis (diagnosis)", "Prostatitis caused by bacteria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bacterial prostatitis", "shortest_name_length": 18}
{"curie": "MONDO:0010618", "names": ["HYPX", "Parathyroid absence", "Parathyroid aplasia", "Parathyroid agenesis", "parathyroid; agenesis", "X-linked hypoparathyroidism", "X-Linked Hypoparathyroidism", "agenesis; parathyroid gland", "X-linked Hypoparathyroidism", "hypoparathyroidism, X-linked", "HYPOPARATHYROIDISM, X-LINKED", "Hypoparathyroidism, X-Linked", "Agenesis of parathyroid gland", "Hypoparathyroidism - X-linked", "agenesis of parathyroid glands", "Parathyroid Glands, Agenesis Of", "PARATHYROID GLANDS, AGENESIS OF", "parathyroid glands, agenesis of", "parathyroid; absence, congenital", "Aplasia of the parathyroid glands", "Congenital absent parathyroid gland", "X-linked hypoparathyroidism (disorder)", "absence; parathyroid gland, congenital", "Congenital absence of parathyroid gland", "Congenital absence of parathyroid gland (disorder)", "familial isolated hypoparathyroidism due to agenesis of parathyroid gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial isolated hypoparathyroidism due to agenesis of parathyroid gland", "shortest_name_length": 4}
{"curie": "MONDO:0021155", "names": ["X-linked cone-rod dystrophy", "cone-rod dystrophy, X-linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked cone-rod dystrophy", "shortest_name_length": 27}
{"curie": "UMLS:C5668171", "names": ["Recurrent Diffuse Large B-Cell Lymphoma Associated with Chronic Inflammation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Diffuse Large B-Cell Lymphoma Associated with Chronic Inflammation", "shortest_name_length": 76}
{"curie": "UMLS:C3898154", "names": ["Necrotizing Enterocolitis Totalis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Necrotizing Enterocolitis Totalis", "shortest_name_length": 33}
{"curie": "MONDO:0001240", "names": ["anemia neonatal", "Neonatal Anemia", "anemia; newborn", "newborn; anemia", "Anemia neonatal", "neonatal anemia", "Neonatal anemia", "ANEMIA NEONATAL", "Neonatal anaemia", "Anaemia neonatal", "Neonatal Anemias", "Anemia, Neonatal", "neonatal anaemia", "ANAEMIA NEONATAL", "anaemia neonatal", "Anemia Neonatorum", "Anemias, Neonatal", "Neonatal anemia, NOS", "Neonatal anaemia, NOS", "Neonatal anemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal anemia", "shortest_name_length": 15}
{"curie": "MONDO:0017192", "names": ["sporadic secreting paraganglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sporadic secreting paraganglioma", "shortest_name_length": 32}
{"curie": "UMLS:C0854381", "names": ["genital bleeding", "Bleeding genital", "Genital bleeding", "bleeding genitals", "Genital hemorrhage", "genital haemorrhage", "Genital haemorrhage", "Genital hemorrhage NOS", "Genital haemorrhage NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Genital hemorrhage", "shortest_name_length": 16}
{"curie": "UMLS:C1333550", "names": ["FIGO Stage IB GTT", "FIGO Stage IB Gestational Trophoblastic Tumor", "FIGO Stage IB Gestational Trophoblastic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Stage IB Gestational Trophoblastic Tumor", "shortest_name_length": 17}
{"curie": "MONDO:0010460", "names": ["MRXS17", "MENTAL RETARDATION, X-LINKED, SYNDROMIC 17", "mental retardation, X-linked, syndromic 17", "syndromic X-linked intellectual disability 17", "intellectual disability, X-linked, syndromic 17", "syndromic X-linked intellectual disability type 17", "intellectual disability-alacrima-achalasia syndrome", "X-linked mental retardation with alacrima and achalasia", "mental retardation, X-linked, with alacrima and achalasia", "MENTAL RETARDATION, X-LINKED, WITH ALACRIMA AND ACHALASIA", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 17", "X-linked intellectual disability with alacrima and achalasia", "mental retardation, X-linked, syndromic 17, X-linked recessive", "intellectual disability, X-linked, with alacrima and achalasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic X-linked intellectual disability 17", "shortest_name_length": 6}
{"curie": "MONDO:0006653", "names": ["Anthracosilicosis", "anthracosilicosis", "Anthracosilicoses", "ANTHRACOSILICOSIS", "Anthracosilicosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anthracosilicosis", "shortest_name_length": 17}
{"curie": "MONDO:0014688", "names": ["SRTD14", "short-rib thoracic dysplasia 14 with polydactyly", "SHORT-RIB THORACIC DYSPLASIA 14 WITH POLYDACTYLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short-rib thoracic dysplasia 14 with polydactyly", "shortest_name_length": 6}
{"curie": "MONDO:0012153", "names": ["AD9", "Alzheimer Disease 9", "Alzheimer disease 9", "Alzheimer's disease 9", "Alzheimer Disease 9, Late-Onset", "Alzheimer disease 9, late-onset", "ALZHEIMER DISEASE 9, LATE-ONSET", "Alzheimer's disease 9, late onset", "Alzheimer disease 9, susceptibility to", "ALZHEIMER DISEASE 9, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alzheimer disease 9", "shortest_name_length": 3}
{"curie": "MONDO:0003885", "names": ["Colorectal Lipoma", "colorectal lipoma", "Large Bowel Lipoma", "large bowel lipoma", "Lipoma of Large Bowel", "lipoma of large bowel", "Large Intestine Lipoma", "large intestine lipoma", "lipoma of the large bowel", "Lipoma of large Intestine", "Lipoma of the Large Bowel", "Lipoma of Large Intestine", "lipoma of large intestine", "Lipoma of large intestine", "lipoma of the large intestine", "Lipoma of the Large Intestine", "Lipoma of large intestine (disorder)", "lipoma of large intestine (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorectal lipoma", "shortest_name_length": 17}
{"curie": "MONDO:0004031", "names": ["mixed ovarian carcinoma", "ovarian seromucinous carcinoma", "ovary mixed epithelial carcinoma", "mixed epithelial carcinoma of Ovary", "mixed epithelial carcinoma of ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovary mixed epithelial carcinoma", "shortest_name_length": 23}
{"curie": "MONDO:0100003", "names": ["AEACEI", "susceptibility to angioedema induced by ACE inhibitors", "angioedema induced by ACE inhibitors, susceptibility to", "ANGIOEDEMA INDUCED BY ACE INHIBITORS, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "susceptibility to angioedema induced by ACE inhibitors", "shortest_name_length": 6}
{"curie": "MONDO:0017126", "names": ["oculo-skeletal-renal syndrome", "oculo skeletal renal syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculo-skeletal-renal syndrome", "shortest_name_length": 29}
{"curie": "MONDO:0009170", "names": ["ENDOCARDIAL FIBROELASTOSIS AND COARCTATION OF ABDOMINAL AORTA", "endocardial fibroelastosis and coarctation of abdominal aorta", "Endocardial Fibroelastosis and Coarctation of Abdominal Aorta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endocardial fibroelastosis and coarctation of abdominal aorta", "shortest_name_length": 61}
{"curie": "UMLS:C0205730", "names": ["Hereditary Opalescent Dentin", "Opalescent Dentin, Hereditary", "Hereditary Opalescent Dentin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hereditary Opalescent Dentin (disorder)", "shortest_name_length": 28}
{"curie": "UMLS:C1336809", "names": ["Transplant-Related Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transplant-Related Disorder", "shortest_name_length": 27}
{"curie": "UMLS:C0475765", "names": ["Nose edema", "NOSE EDEMA", "nasal edema", "Nasal edema", "Nose oedema", "NOSE OEDEMA", "Nasal oedema", "Swollen nasal mucosa", "nasal edema was noted", "edematous nasal mucosa", "Nasal mucosal swelling", "Nasal mucosa edematous", "Nasal mucosa oedematous", "nasal mucosa hypertrophy", "NOSE MUCOUS MEMBRANE SWELLING", "Swollen nasal mucosa (finding)", "nasal edema (physical finding)", "Nasal mucosa edematous (finding)", "edematous nasal mucosa (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Swollen nasal mucosa (finding)", "shortest_name_length": 10}
{"curie": "UMLS:C0520539", "names": ["HYPERTENSIVE EPISODE", "Hypertensive episode", "hypertensive episode", "Hypertensive Episode", "Hypertensive episodes", "hypertensive episode (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypertensive episode", "shortest_name_length": 20}
{"curie": "UMLS:C0162164", "names": ["PULMONIC STENOSIS CONGENITAL", "Congenital pulmonic valve stenosis", "congenital pulmonary valve stenosis", "Congenital pulmonary valve stenosis", "Pulmonary valve stenosis congenital", "pulmonary valve; deformity, stenosis", "Congenital pulmonary valvar stenosis", "deformity; pulmonary valve, stenosis", "stenosis; pulmonary valve, congenital", "Congenital valvular pulmonic stenosis", "congenital pulmonary valvular stenosis", "Congenital stenosis of pulmonary valve", "pulmonary valve; stricture, congenital", "stricture; pulmonary valve, congenital", "Stenosis of pulmonary valve, congenital", "PV - Congenital pulmonary valve stenosis", "congenital pulmonary valve stenosis (diagnosis)", "Congenital valvular stenosis of pulmonary valve", "pulmonary; stricture pulmonary valve, congenital", "Congenital stenosis of pulmonary valve (disorder)", "Congenital valvular stenosis of pulmonary valve (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital stenosis of pulmonary valve", "shortest_name_length": 28}
{"curie": "MONDO:0019623", "names": ["HAE", "HANE", "hane", "Quincke; hereditary", "hereditary; Quincke", "angioedema hereditary", "hereditary angioedema", "Hereditary angioedema", "HEREDITARY ANGIOEDEMA", "hereditary; Bannister", "Hereditary Angioedema", "Bannister; hereditary", "Hereditary angio-edema", "hereditary; angioedema", "Angioedema, Hereditary", "angioedema, hereditary", "ANGIOEDEMA, HEREDITARY", "hereditary angio-edema", "Hereditary Angioedemas", "angio edema hereditary", "angioedema; hereditary", "C1 inhibitor deficiency", "hereditary angio-oedema", "Hereditary angio-oedema", "c1 inhibitor deficiency", "Angioedemas, Hereditary", "C1 Inhibitor Deficiency", "Hereditary Quincke's edema", "edema; Quincke, hereditary", "Quincke; edema, hereditary", "HAE - Hereditary angioedema", "Hereditary Quincke's oedema", "Familial angioneurotic edema", "familial angioneurotic edema", "HAE - Hereditary angio-edema", "HAE - Hereditary angio-oedema", "complement esterase deficiency", "hereditary angioneurotic edema", "Hereditary Angioneurotic Edema", "Hereditary angioneurotic edema", "hereditary; angioneurotic edema", "Hereditary angioneurotic oedema", "Hereditary Angioneurotic Edemas", "Angioneurotic Edema, Hereditary", "ANGIONEUROTIC EDEMA, HEREDITARY", "Edema, Hereditary Angioneurotic", "c1 esterase inhibitor deficiency", "Angioneurotic Edemas, Hereditary", "C1 esterase inhibitor deficiency", "edema; angioneurotic, hereditary", "Edemas, Hereditary Angioneurotic", "C1 Esterase Inhibitor Deficiency", "Hereditary angioedema (disorder)", "angioneurotic; edema, hereditary", "C1 ESTERASE INHIBITOR DEFICIENCY", "Hereditary angioedema (diagnosis)", "deficiency; C1 esterase inhibitor", "C-1 esterase inhibitor deficiency", "C1 esterase inhibitor; deficiency", "deficiency of C1 esterase inhibitor", "C1 inhibitor deficiency (diagnosis)", "HANE - Hereditary angioneurotic edema", "HANE - Hereditary angioneurotic oedema", "hereditary bradykinine-induced angioedema", "Hereditary bradykinine-induced angioedema", "C-1 esterase inhibitor deficiency syndrome", "Hereditary non histamine-induced angioedema", "hereditary non histamine-induced angioedema", "Hereditary angioedema C1 inhibitor deficiency", "C1 inhibitor deficiency with hereditary angioedema", "C1 inhibitor deficiency with hereditary angioedema (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary angioedema", "shortest_name_length": 3}
{"curie": "MONDO:0001475", "names": ["neutropenia", "Neutropenia", "NEUTROPENIA", "Neutropenias", "Neutropenia, NOS", "Neutropenic disorder", "neutropenic disorder", "NEUTROPHILS DECREASED", "neutropenia (diagnosis)", "Neutropenia, unspecified", "Neutropenic disorder (disorder)", "Disorder characterized by neutropenia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neutropenia", "shortest_name_length": 11}
{"curie": "UMLS:C4524634", "names": ["Esophageal Adenocarcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Adenocarcinoma by AJCC v7 Stage", "shortest_name_length": 42}
{"curie": "MONDO:0007101", "names": ["FPLCA", "amyloidosis IX", "primary localized cutaneous amyloidosis", "hereditary primary cutaneous amyloidosis", "familial primary localized cutaneous amyloidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial primary localized cutaneous amyloidosis", "shortest_name_length": 5}
{"curie": "MONDO:0008227", "names": ["PERIPHERAL DYSOSTOSIS", "dysostosis peripheral", "Peripheral dysostosis", "Peripheral Dysostosis", "peripheral dysostosis", "Peripheral dysostosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peripheral dysostosis", "shortest_name_length": 21}
{"curie": "MONDO:0015424", "names": ["Moerman-Vandenberghe-Fryns syndrome", "lethal chondrodysplasia Moerman type", "lethal chondrodysplasia, Moerman type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal chondrodysplasia, Moerman type", "shortest_name_length": 35}
{"curie": "MONDO:0800094", "names": ["dysostosis with brachydactyly with extraskeletal manifestations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dysostosis with brachydactyly with extraskeletal manifestations", "shortest_name_length": 63}
{"curie": "MONDO:0006265", "names": ["larynx small cell carcinoma", "Larynx Small Cell Carcinoma", "laryngeal small cell carcinoma", "small cell carcinoma of larynx", "Laryngeal Small Cell Carcinoma", "Small Cell Carcinoma of Larynx", "small cell carcinoma of Larynx", "small cell carcinoma of the larynx", "Small Cell Carcinoma of the Larynx", "laryngeal throat small cell cancer", "Laryngeal Throat Small Cell Cancer", "small cell carcinoma of larynx (diagnosis)", "Laryngeal Small Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laryngeal small cell carcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C5237270", "names": ["Locally Advanced Pharyngeal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Pharyngeal Carcinoma", "shortest_name_length": 37}
{"curie": "UMLS:C1504443", "names": ["Instillation site reaction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Instillation site reaction", "shortest_name_length": 26}
{"curie": "MONDO:0007539", "names": ["Neuhauser Eichner Opitz syndrome", "Neuhauser-Eichner-Opitz syndrome", "Recurrent encephalopathy of childhood", "encephalopathy recurrent of childhood", "Recurrent encephalophathy of childhood", "ENCEPHALOPATHY, RECURRENT, OF CHILDHOOD", "encephalopathy, recurrent, of childhood", "Encephalopathy, recurrent, of childhood", "Neuhauser Eichner Opitz syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephalopathy, recurrent, of childhood", "shortest_name_length": 32}
{"curie": "UMLS:C1335442", "names": ["Poorly Differentiated Fibrosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Poorly Differentiated Fibrosarcoma", "shortest_name_length": 34}
{"curie": "MONDO:0004326", "names": ["sphenoid sinus inverted papilloma", "Sphenoid Sinus Inverted Papilloma", "sphenoidal sinus inverted papilloma", "Inverted Papilloma of Sphenoid Sinus", "inverted papilloma of sphenoid sinus", "inverted papilloma of the sphenoid sinus", "Inverted Papilloma of the Sphenoid Sinus", "Inverted papilloma of the Sphenoid sinus", "Sphenoid Sinus Inverted Schneiderian Papilloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sphenoid sinus inverted papilloma", "shortest_name_length": 33}
{"curie": "UMLS:C4520902", "names": ["Stage 0 Nasopharynx Keratinizing Epidermoid Carcinoma", "Nasopharynx Keratinizing Epidermoid Carcinoma in situ", "Stage 0 Keratinizing Epidermoid Carcinoma of Nasopharynx", "Nasopharynx Keratinizing Squamous Cell Carcinoma in situ", "Stage 0 Nasopharynx Keratinizing Squamous Cell Carcinoma", "Stage 0 Nasopharyngeal Keratinizing Epidermoid Carcinoma", "Nasopharyngeal Keratinizing Epidermoid Carcinoma in situ", "Keratinizing Epidermoid Carcinoma in situ of Nasopharynx", "Stage 0 Keratinizing Squamous Cell Carcinoma of Nasopharynx", "Nasopharyngeal Keratinizing Squamous Cell Carcinoma in situ", "Keratinizing Squamous Cell Carcinoma in situ of Nasopharynx", "Stage 0 Nasopharyngeal Keratinizing Squamous Cell Carcinoma", "Stage 0 Keratinizing Epidermoid Carcinoma of the Nasopharynx", "Keratinizing Epidermoid Carcinoma in situ of the Nasopharynx", "Keratinizing Squamous Cell Carcinoma in situ of the Nasopharynx", "Stage 0 Keratinizing Squamous Cell Carcinoma of the Nasopharynx", "Stage 0 Nasopharyngeal Throat Keratinizing Squamous Cell Cancer", "Stage 0 Nasopharyngeal Keratinizing Squamous Cell Carcinoma AJCC v8", "Stage 0 Nasopharyngeal Keratinizing Squamous Cell Carcinoma AJCC v7", "Stage 0 Nasopharyngeal Keratinizing Squamous Cell Carcinoma AJCC v6", "Stage 0 Nasopharyngeal Keratinizing Squamous Cell Carcinoma AJCC v6, v7, and v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Nasopharyngeal Keratinizing Squamous Cell Carcinoma AJCC v6, v7, and v8", "shortest_name_length": 53}
{"curie": "UMLS:C0431095", "names": ["Adenocarcinoma with Metaplasia", "Adenocarcinoma with metaplasia", "adenocarcinoma with metaplasia", "adenocarcinoma with metaplasia (diagnosis)", "Adenocarcinoma with metaplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma with metaplasia", "shortest_name_length": 30}
{"curie": "MONDO:0008990", "names": ["Novak syndrome", "Congenital stridor", "congenital; stridor", "STRIDOR, CONGENITAL", "stridor, congenital", "stridor; congenital", "Stridor, Congenital", "cleft larynx, posterior", "CLEFT LARYNX, POSTERIOR", "Cleft larynx, posterior", "Laryngotracheoesophageal cleft pulmonary hypoplasia", "laryngotracheoesophageal cleft pulmonary hypoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleft larynx, posterior", "shortest_name_length": 14}
{"curie": "MONDO:0013348", "names": ["RP65", "CORD15", "CONE-ROD DYSTROPHY 15", "cone-rod dystrophy 15", "retinitis pigmentosa 65", "RETINITIS PIGMENTOSA 65", "CDHR1 cone-rod dystrophy", "cone-rod dystrophy type 15", "cone-rod dystrophy caused by mutation in CDHR1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cone-rod dystrophy 15", "shortest_name_length": 4}
{"curie": "UMLS:C0345704", "names": ["Pyriform Fossa Tumor", "Pyriform Sinus Tumor", "Tumor of pyriform fossa", "Pyriform Sinus Neoplasm", "Tumor of Pyriform Fossa", "Pyriform Fossa Neoplasm", "Tumor of Pyriform Sinus", "Tumour of pyriform fossa", "Neoplasm of Pyriform Sinus", "Neoplasm of pyriform sinus", "Neoplasm of Pyriform Fossa", "Tumor of the Pyriform Fossa", "Tumor of the Pyriform Sinus", "Neoplasm of the Pyriform Fossa", "Neoplasm of the Pyriform Sinus", "Neoplasm of pyriform sinus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplasm of pyriform sinus", "shortest_name_length": 20}
{"curie": "MONDO:0004232", "names": ["large cell keratinizing variant squamous cell breast carcinoma", "squamous cell breast carcinoma, large cell keratinizing variant", "Breast Squamous Cell Carcinoma, Large Cell Keratinizing Variant", "Squamous Cell Breast Carcinoma, Large Cell Keratinizing Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "large cell keratinizing variant squamous cell breast carcinoma", "shortest_name_length": 62}
{"curie": "NCIT:C171452", "names": ["epidemic", "Epidemic", "Epidemic Disease", "Epidemic Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epidemic Disorder", "shortest_name_length": 8}
{"curie": "MONDO:0016512", "names": ["NKS", "KMS", "KABUK1", "kabuki syndrome", "Kabuki syndrome", "Kabuki Syndrome", "KABUKI SYNDROME", "KABUKI SYNDROME 1", "Kabuki syndrome (KS)", "Kabuki Makeup Syndrome", "NIIKAWA-KUROKI SYNDROME", "Kabuki Make-up Syndrome", "niikawa-kuroki syndrome", "Kabuki Make-Up Syndrome", "Niikawa-Kuroki Syndrome", "Kabuki make-up syndrome", "Kabuki make up syndrome", "KABUKI MAKE-UP SYNDROME", "kabuki make-up syndrome", "kabuki make up syndrome", "Niikawa-Kuroki syndrome", "Kabuki syndrome (diagnosis)", "Kabuki make-up syndrome (KMS)", "Kabuki make-up syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kabuki syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0000170", "names": ["MAC", "MCOPCB1", "colobomatous microphthalmia", "microphthalmia with colobomatous cyst", "microphthalmia, isolated, with coloboma", "microphthalmia-anophthalmia-coloboma syndrome", "Microphthalmia associated with colobomatous cyst", "microphthalmia associated with colobomatous cyst", "microphthalmos bilateral, colobomatous orbital cyst", "Microphthalmos bilateral, colobomatous orbital cyst"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microphthalmia, isolated, with coloboma", "shortest_name_length": 3}
{"curie": "MONDO:0005147", "names": ["T1D", "IDD", "JOD", "T1d", "T1D1", "jodm", "iddm", "IDDM", "IDDM1", "type I diabetes", "Diabetes Type 1", "diabetes type i", "Type 1 diabetes", "Type I diabetes", "type 1 diabetes", "type i diabetes", "Type 1 Diabetes", "diabetes type 1", "Type I Diabetes", "Diabetes;Type 1", "Diabetes, Type 1", "Diabetes, type 1", "diabetes, type i", "type I; diabetes", "diabetes; type I", "Juvenile diabetes", "Juvenile Diabetes", "juvenile diabetes", "Juvenile Onset Diabetes", "Diabetes;juvenile onset", "JUVENILE-ONSET DIABETES", "Juvenile-Onset Diabetes", "Diabetes mellitus Type I", "diabetes mellitis type 1", "type 1 diabetes mellitus", "type i diabetes mellitus", "Diabetes mellitus type 1", "Type 1 diabetes mellitus", "Immune-mediated diabetes", "TYPE 1 DIABETES MELLITUS", "immune mediated diabetes", "Diabetes mellitus type I", "type I diabetes mellitus", "Type I Diabetes Mellitus", "Type I diabetes mellitus", "Diabetes, Juvenile-Onset", "diabetes mellitus type 1", "diabetes; juvenile-onset", "diabetes mellitus type i", "juvenile-onset; diabetes", "Immune Mediated Diabetes", "diabetes mellitis type I", "Type 1 Diabetes Mellitus", "Diabetes Mellitus, Type I", "Diabetes mellitus, Type 1", "DIABETES MELLITUS, TYPE 1", "DIABETES MELLITUS, TYPE I", "Diabetes mellitus, type I", "Diabetes mellitus, type 1", "Diabetes Mellitus, Type 1", "Insulin Dependent Diabetes", "TYPE 1 DIABETES MELLITUS 1", "juvenile onset of diabetes", "Diabetes insulin dependent", "Insulin dependent diabetic", "Juvenile diabetes mellitus", "juvenile diabetes mellitus", "insulin dependent diabetes", "Diabetes;insulin dependent", "Diabetes Mellitus (Type I)", "Insulin-dependent diabetes", "brittle diabetes (mellitus)", "diabetes; insulin-dependent", "insulin-dependent; diabetes", "Diabetes, Type I+A3139:G3152", "Sudden-Onset Diabetes Mellitus", "Diabetes Mellitus, Sudden-Onset", "T1DM - type 1 diabetes mellitus", "Diabetes Mellitus, Sudden Onset", "JUVENILE ONSET DIABETES MELLITUS", "juvenile-onset diabetes mellitus", "Juvenile-Onset Diabetes Mellitus", "Juvenile onset diabetes mellitus", "juvenile onset diabetes mellitus", "Diabetes mellitus juvenile onset", "Diabetes Mellitus, Juvenile Onset", "Diabetes Mellitus, Juvenile-Onset", "obsolete_type I diabetes mellitus", "juvenile onset diabetes (mellitus)", "DIABETES MELLITUS (JUVENILE ONSET)", "insulin dependent diabetes mellitus", "Insulin-Dependent Diabetes Mellitus", "Diabetes mellitus insulin-dependent", "Insulin-dependent diabetes mellitus", "Insulin dependent diabetes mellitus", "Insulin Dependent Diabetes Mellitus", "insulin-dependent diabetes mellitus", "Diabetes mellitus type 1 (disorder)", "DIABETES MELLITUS INSULIN DEPENDENT", "Diabetes Mellitus, Insulin Dependent", "DIABETES MELLITUS, INSULIN-DEPENDENT", "Diabetes mellitus, insulin-dependent", "Diabetes mellitus, growth onset type", "DIABETES MELLITUS, INSULIN DEPENDENT", "Diabetes Mellitus, Insulin-Dependent", "Type 1 diabetes mellitus (diagnosis)", "Insulin-Dependent Diabetes Mellitus 1", "Insulin Dependent Diabetes Mellitus 1", "INSULIN-DEPENDENT DIABETES MELLITUS 1", "Diabetes mellitus, juvenile onset type", "Diabetes Mellitus, Insulin-Dependent, 1", "DIABETES MELLITUS, INSULIN-DEPENDENT, 1", "IDDM - Insulin-dependent diabetes mellitus", "Insulin-dependent diabetes mellitus (type I)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type 1 diabetes mellitus", "shortest_name_length": 3}
{"curie": "MONDO:0015463", "names": ["Scott craniodigital syndrome", "Scott-Bryant-Graham syndrome", "Scott Bryant Graham syndrome", "Craniodigital syndrome with mental retardation", "craniodigital syndrome with mental retardation", "craniodigital-intellectual disability syndrome", "Craniodigital-intellectual disability syndrome", "craniodigital syndrome with intellectual disability", "SCOTT CRANIODIGITAL SYNDROME WITH MENTAL RETARDATION", "Scott craniodigital syndrome with mental retardation", "Craniodigital syndrome-mental retardation, Scott type", "craniodigital syndrome-mental retardation, Scott type", "craniodigital syndrome-intellectual disability syndrome", "Scott craniodigital syndrome with intellectual disability", "craniodigital syndrome-intellectual disability, Scott type", "craniodigital syndrome and intellectual disability syndrome", "Craniodigital syndrome and intellectual disability syndrome", "Craniodigital syndrome and intellectual disability syndrome (disorder)", "craniodigital syndrome and intellectual disability syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniodigital syndrome-intellectual disability syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0018864", "names": ["Kikuchi disease", "Kikuchi Disease", "kikuchi disease", "Kikuchis Disease", "Disease, Kikuchi", "kikuchis disease", "Kikuchi's Disease", "kikuchi's disease", "Kikuchi's disease", "Disease, Kikuchi's", "kikuchi-fujimoto disease", "Kikuchi-Fujimoto disease", "kikuchi fujimoto disease", "Kikuchi-Fujimoto Disease", "Kikuchi Fujimoto Disease", "Disease, Kikuchi-Fujimoto", "Kikuchi-Fujimotos Disease", "Kikuchi-Fujimoto's Disease", "Kikuchi Fujimoto's Disease", "Kikuchi-Fujimoto's disease", "Nosocomial Kikuchi Disease", "Nosocomial Kikuchis Disease", "Disease, Kikuchi-Fujimoto's", "nosocomial Kikuchi's disease", "Nosocomial Kikuchi's Disease", "Kikuchi's Disease, Nosocomial", "Kikuchi Necrotizing Lymphadenitis", "Kikuchi necrotizing lymphadenitis", "Necrotizing Lymphadenitis, Kikuchi", "Lymphadenitis, Kikuchi Necrotizing", "Subacute necrotizing lymphadenitis", "Subacute necrotising lymphadenitis", "Histiocytic necrotising lymphadenitis", "Histiocytic Necrotising Lymphadenitis", "histiocytic necrotising lymphadenitis", "Histiocytic Necrotizing Lymphadenitis", "histiocytic necrotizing lymphadenitis", "Histiocytic necrotizing lymphadenitis", "Necrotising Lymphadenitis, Histiocytic", "Lymphadenitis, Histiocytic Necrotising", "Necrotizing Lymphadenitis, Histiocytic", "Lymphadenitis, Histiocytic Necrotizing", "Histiocytic necrotizing lymphadenopathy", "Histiocytic Necrotising Lymphadenitides", "Histiocytic necrotising lymphadenopathy", "Necrotising Lymphadenitides, Histiocytic", "Lymphadenitides, Histiocytic Necrotising", "Histiocytic necrotizing lymphadenitis (disorder)", "histiocytic necrotizing lymphadenitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kikuchi-Fujimoto disease", "shortest_name_length": 15}
{"curie": "MONDO:0003174", "names": ["spinal astrocytoma", "Spinal astrocytoma", "Spinal Astrocytoma", "Spinal Cord Astrocytoma", "astrocytoma spinal cord", "spinal cord astrocytoma", "Astrocytoma of spinal cord", "astrocytoma of spinal cord", "Astrocytoma of Spinal Cord", "astrocytoma of the spinal cord", "Astrocytoma of the Spinal Cord", "Astrocytic tumor of spinal cord", "Astrocytic tumour of spinal cord", "Astrocytoma of spinal cord (disorder)", "spinal cord astrocytoma (excluding glioblastoma)", "astrocytoma (excluding glioblastoma) of spinal cord"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal cord astrocytoma", "shortest_name_length": 18}
{"curie": "UMLS:C2987419", "names": ["Gastric foveolar", "Foveolar-Type Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Foveolar-Type Adenoma", "shortest_name_length": 16}
{"curie": "UMLS:C5205118", "names": ["Unresectable Lung Small Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Lung Small Cell Carcinoma", "shortest_name_length": 38}
{"curie": "UMLS:C1332644", "names": ["Burkitt Lymphoma with Plasmacytoid Differentiation", "Burkitt's Lymphoma with Plasmacytoid Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Burkitt Lymphoma with Plasmacytoid Differentiation", "shortest_name_length": 50}
{"curie": "MONDO:0014029", "names": ["OI14", "OI, type 14", "OI, TYPE XIV", "osteogenesis imperfecta type 14", "TMEM38B osteogenesis imperfecta", "osteogenesis imperfecta, type 14", "osteogenesis imperfecta type XIV", "osteogenesis imperfecta, type XIV", "OSTEOGENESIS IMPERFECTA, TYPE XIV", "osteogenesis imperfecta caused by mutation in TMEM38B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteogenesis imperfecta type 14", "shortest_name_length": 4}
{"curie": "MONDO:0003181", "names": ["LUACC", "lung adenocystic carcinoma", "Lung Adenoid Cystic Cancer", "lung adenoid cystic cancer", "Lung Adenocystic Carcinoma", "lung adenoid cystic carcinoma", "Lung Adenoid Cystic Carcinoma", "adenocystic carcinoma of lung", "Adenocystic Carcinoma of Lung", "pulmonary adenocystic carcinoma", "Pulmonary Adenocystic Carcinoma", "adenoid cystic carcinoma of lung", "Adenoid cystic carcinoma of lung", "Adenoid Cystic Carcinoma of Lung", "Adenocystic Carcinoma of the Lung", "adenocystic carcinoma of the lung", "pulmonary adenoid cystic carcinoma", "Pulmonary Adenoid Cystic Carcinoma", "Adenoid Cystic Carcinoma of the Lung", "adenoid cystic carcinoma of the lung", "Primary adenoid cystic carcinoma of lung", "Adenoid cystic carcinoma of lung (disorder)", "adenoid cystic carcinoma of lung (diagnosis)", "Primary adenoid cystic carcinoma of lung (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung adenoid cystic carcinoma", "shortest_name_length": 5}
{"curie": "UMLS:C5206635", "names": ["HPV-Related PeIN", "Human Papillomavirus-Related PeIN", "Human Papillomavirus-Related Penile Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Human Papillomavirus-Related Penile Intraepithelial Neoplasia", "shortest_name_length": 16}
{"curie": "MONDO:0008984", "names": ["RUTLAND CILIARY DISORIENTATION SYNDROME", "Rutland ciliary disorientation syndrome", "Rutland Ciliary Disorientation Syndrome", "Rutland ciliary disorientation syndrome (disorder)", "CILIARY DISCOORDINATION DUE TO RANDOM CILIARY ORIENTATION", "ciliary discoordination due to random ciliary orientation", "Ciliary Discoordination Due To Random Ciliary Orientation", "ciliary discoordination, due to random ciliary orientation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ciliary discoordination due to random ciliary orientation", "shortest_name_length": 39}
{"curie": "UMLS:C0879626", "names": ["side effect", "Side Effect", "Side effects", "side effects", "adverse effect", "adverse effects", "Adverse effects", "Treatment Side Effects", "treatment side effects", "Treatment side effects", "therapy adverse effect", "treatment adverse effect", "Side Effects (Treatment)", "treatment adverse effects", "treatment harmful effects", "Adverse effect, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adverse effects", "shortest_name_length": 11}
{"curie": "UMLS:C5418955", "names": ["Unresectable Fallopian Tube Serous Adenocarcinoma", "Unresectable Fallopian Tube High Grade Serous Adenocarcinoma", "Unresectable High Grade Fallopian Tube Serous Adenocarcinoma", "Unresectable High-Grade Fallopian Tube Serous Adenocarcinoma", "Unresectable Fallopian Tube High-Grade Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Fallopian Tube High Grade Serous Adenocarcinoma", "shortest_name_length": 49}
{"curie": "UMLS:C0158687", "names": ["genital malformation", "Genital malformation", "GENITAL MALFORMATION", "genital malformations", "Genital malformation, NOS", "anomalies of genital organs", "Congenital genital malformation", "congenital genital malformations", "Congenital genital organ anomalies", "Congenital genital malformation NOS", "Congenital anomaly of genital organ", "Congenital deformity of genital organ", "Unspecified anomaly of genital organs", "Congenital anomalies of genital organs", "anomalies of genital organs (diagnosis)", "Congenital anomaly of genital organ, NOS", "Congenital malformation of genital organs", "Congenital deformity of genital organ, NOS", "Congenital malformations of genital organs", "Congenital anomaly NOS of genital organ, NEC", "Congenital deformity NOS of genital organ, NEC", "Unspecified congenital anomaly of genital organs", "Congenital malformations of genital organs (Q50-Q56)", "Congenital malformation of genital organs (disorder)", "CONGENITAL ANOMALIES OF THE MALE AND FEMALE GENITAL SYSTEMS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital malformation of genital organs", "shortest_name_length": 20}
{"curie": "MONDO:0030974", "names": ["MC2DN4", "mitochondrial complex 2 deficiency, nuclear type 4", "mitochondrial complex II deficiency, nuclear type 4", "MITOCHONDRIAL COMPLEX II DEFICIENCY, NUCLEAR TYPE 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 2 deficiency, nuclear type 4", "shortest_name_length": 6}
{"curie": "MONDO:0011897", "names": ["HLD7", "ADDH", "4H syndrome", "4H SYNDROME", "TACH syndrome", "4H LEUKODYSTROPHY 1", "dentoleukoencephalopathy", "leukodystrophy with oligodontia", "hypomyelinating leukodystrophy 7", "Leukodystrophy, Hypomyelinating, 7", "Ataxia, Delayed Dentition, and Hypomyelination", "tremor-ataxia-central hypomyelination syndrome", "ataxia, delayed dentition, and hypomyelination", "ATAXIA, DELAYED DENTITION, AND HYPOMYELINATION", "ataxia-delayed dentition-hypomyelination syndrome", "leukoencephalopathy-ataxia-hypodontia-hypomyelination syndrome", "Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome", "Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome", "Leukoencephalopathy, Hypomyelinating, with Ataxia and Delayed Dentition", "leukoencephalopathy, hypomyelinating, with ataxia and delayed dentition", "ataxia-delayed dentition-hypomyelination syndrome; odontoleukodystrophy", "LEUKOENCEPHALOPATHY, HYPOMYELINATING, WITH ATAXIA AND DELAYED DENTITION", "hypomyelinating leukodystrophy-ataxia-hypodontia-hypomyelination syndrome", "hypomyelination-cerebellar atrophy-hypoplasia of the corpus callosum syndrome", "Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome (disorder)", "Leukodystrophy, Hypomyelinating, with Hypodontia and Hypogonadotropic Hypogonadism", "LEUKODYSTROPHY, HYPOMYELINATING, WITH HYPODONTIA AND HYPOGONADOTROPIC HYPOGONADISM", "leukodystrophy, hypomyelinating, with hypodontia and hypogonadotropic hypogonadism", "hypomyelinating leukodystrophy 7 with or without oligodontia and-or hypogonadotropic hypogonadism", "leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism", "LEUKODYSTROPHY, HYPOMYELINATING, 7, WITH OR WITHOUT OLIGODONTIA AND/OR HYPOGONADOTROPIC HYPOGONADISM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukoencephalopathy-ataxia-hypodontia-hypomyelination syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0017268", "names": ["acral SHCB", "Acral SHCB", "acral self-healing collodion baby", "Acral self-healing collodion baby", "Acral self-healing collodion baby (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acral self-healing collodion baby", "shortest_name_length": 10}
{"curie": "UMLS:C0339434", "names": ["Choroidal Effusion", "Choroidal effusion", "Choroidal Effusions", "Effusion, Choroidal", "Ciliochoroidal Effusion", "Ciliochoroidal Effusions", "Effusion, Ciliochoroidal", "Choroidal effusion (disorder)", "choroidal detachment effusion", "Choroidal effusion (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Choroidal Effusions", "shortest_name_length": 18}
{"curie": "UMLS:C4553618", "names": ["Stage IVA Vaginal Cancer", "Stage IVA Vaginal Cancer AJCC v8", "Stage IVA Vaginal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Vaginal Cancer AJCC v8", "shortest_name_length": 24}
{"curie": "UMLS:C0235272", "names": ["Retinal Injury", "retinal damage", "Retinal damage", "RETINAL DAMAGE", "Retinal Damage", "Retinal damage NOS", "Retinal damage, NOS", "Retinal damage (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retinal damage", "shortest_name_length": 14}
{"curie": "MONDO:0008902", "names": ["Camptodactyly-ichthyosis syndrome", "camptodactyly ichthyosis syndrome", "Camptodactyly ichthyosis syndrome", "camptodactyly-ichthyosis syndrome", "CAMPTODACTYLY-ICHTHYOSIS SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "camptodactyly-ichthyosis syndrome", "shortest_name_length": 33}
{"curie": "MONDO:0020452", "names": ["IVC interruption", "Interrupted inferior vena cava", "Interrupted posterior vena cava", "inferior vena cava interruption", "Inferior vena cava interruption", "Inferior caval vein interruption", "Congenital atresia of inferior vena cava", "Congenital atresia of inferior vena cava (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inferior vena cava interruption", "shortest_name_length": 16}
{"curie": "UMLS:C0270217", "names": ["Inspissated Bile Syndrome", "inspissated bile syndrome", "Inspissated bile syndrome", "syndrome; inspissated bile", "inspissated bile; syndrome", "Perinatal inspissated bile syndrome", "perinatal jaundice from inspissated bile", "Perinatal Jaundice due to Inspissated Bile Syndrome", "Perinatal jaundice due to inspissated bile syndrome", "perinatal jaundice from inspissated bile (diagnosis)", "Perinatal Jaundice Related to Inspissated Bile Syndrome", "Perinatal jaundice due to inspissated bile syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perinatal jaundice due to inspissated bile syndrome", "shortest_name_length": 25}
{"curie": "UMLS:C2717899", "names": ["DVT of upper extremity", "Deep venous thrombosis arm", "Upper Extremity Deep Vein Thrombosis", "UPPER EXTREMITY THROMBOSIS DEEP VENOUS", "Deep venous thrombosis of upper extremity", "thrombosis of deep veins of upper extremity", "venous thrombosis upper extremity deep veins", "Deep venous thrombosis of upper extremity (disorder)", "thrombosis of deep veins of upper extremity (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Upper Extremity Deep Vein Thrombosis", "shortest_name_length": 22}
{"curie": "MONDO:0006637", "names": ["Tubulorrhexis", "Acute tubule necrosis", "acute tubule necrosis", "acute tubular necrosis", "acute necrosis tubular", "Acute tubular necrosis", "TUBULAR NECROSIS ACUTE", "Renal tubular necrosis", "Acute Tubular Necrosis", "ACUTE TUBULAR NECROSIS", "Lower nephron nephrosis", "Lower Nephron Nephrosis", "NEPHROSIS LOWER NEPHRON", "LOWER NEPHRON NEPHROSIS", "lower nephron nephrosis", "Lower Nephron Nephroses", "Nephrosis lower nephron", "Nephrosis, Lower Nephron", "Nephron Nephroses, Lower", "Nephroses, Lower Nephron", "Nephron Nephrosis, Lower", "Acute ischemic nephropathy", "Acute tubular necrosis, NOS", "acute renal tubular necrosis", "RENAL TUBULAR NECROSIS ACUTE", "Acute renal tubular necrosis", "ATN - acute tubular necrosis", "ATN - Acute tubular necrosis", "Renal tubular necrosis acute", "acute kidney tubular necrosis", "Acute Kidney Tubular Necrosis", "Kidney Tubular Necrosis, Acute", "Renal tubular epithelial necrosis", "Acute tubular necrosis (disorder)", "acute renal failure with tubular necrosis", "Acute renal failure with tubular necrosis", "Acute Renal Failure with Tubular Necrosis", "acute renal Failure with tubular necrosis", "insufficiency; renal, acute, with necrosis, tubular", "insufficiency; renal, with tubular necrosis (acute)", "acute renal failure with lesion of tubular necrosis", "kidney; insufficiency, acute, with necrosis, tubular", "kidney; insufficiency, with tubular necrosis (acute)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute kidney tubular necrosis", "shortest_name_length": 13}
{"curie": "UMLS:C0235915", "names": ["Pulmonary malformation", "pulmonary malformation", "malformation pulmonary", "PULMONARY MALFORMATION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pulmonary malformation", "shortest_name_length": 22}
{"curie": "MONDO:0001691", "names": ["laryngeal cartilage cancer", "cancer of laryngeal cartilage", "malignant tumor of cartilage of larynx", "malignant laryngeal cartilage neoplasm", "Malignant tumor of laryngeal cartilage", "malignant tumor of laryngeal cartilage", "Malignant tumour of laryngeal cartilage", "malignant neoplasm of laryngeal cartilage", "Malignant neoplasm of laryngeal cartilage", "malignant neoplasm of cartilage of larynx", "malignant neoplasm of laryngeal cartilages", "Malignant neoplasm of laryngeal cartilages", "Malignant tumor of laryngeal cartilage (disorder)", "malignant neoplasm of cartilage of larynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laryngeal cartilage cancer", "shortest_name_length": 26}
{"curie": "UMLS:C0595862", "names": ["vasodilation", "VASODILATION", "vasodilations", "VASODILATATION", "Vasodilatation", "vasodilatation", "Vascular dilation", "vascular dilation", "Vasodilation disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vasodilation disorder", "shortest_name_length": 12}
{"curie": "MONDO:0015607", "names": ["partial deletion of Y", "Y chromosome deletion", "Partial deletion of Y", "Y chromosome deletions", "Y-chromosome microdeletions", "Y chromosome microdeletions", "Partial chromosome Y deletion", "partial chromosome Y deletion", "partial deletion of chromosome Y", "Partial deletion of chromosome Y", "Partial chromosome Y deletion (disorder)", "partial deletion of Y chromosome short arm", "Male sterility due to chromosome Y deletion", "Male sterility due to Y-chromosome deletions", "partial deletion of the long arm of the Y chromosome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial chromosome Y deletion", "shortest_name_length": 21}
{"curie": "UMLS:C3272760", "names": ["Appendix SSA", "Appendix SSP", "Appendix SSA/P", "Appendix Sessile Serrated Polyp", "Appendix Sessile Serrated Adenoma", "Appendix Serrated Lesions and Polyps", "Appendix Sessile Serrated Adenoma/Polyp"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Appendix Serrated Lesions and Polyps", "shortest_name_length": 12}
{"curie": "MONDO:0013775", "names": ["THPH12", "THBD-related coagulopathy", "THBD-related bleeding disorder", "Thrombomodulin-related coagulopathy", "thrombomodulin-related coagulopathy", "Thrombomodulin-related bleeding disorder", "thrombomodulin-related bleeding disorder", "THROMBOPHILIA DUE TO THROMBOMODULIN DEFECT", "Thrombophilia due to Thrombomodulin Defect", "thrombophilia due to thrombomodulin defect", "thrombophilia 12 due to thrombomodulin defect", "THBD (thrombomodulin) related bleeding disorder", "Thrombomodulin-related bleeding disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombomodulin-related bleeding disorder", "shortest_name_length": 6}
{"curie": "UMLS:C4721653", "names": ["Stage I Ovarian Dysgerminoma", "Stage I Ovarian Dysgerminoma AJCC v6", "Stage I Ovarian Dysgerminoma AJCC v7", "Stage I Ovarian Dysgerminoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Ovarian Dysgerminoma AJCC v6 and v7", "shortest_name_length": 28}
{"curie": "MONDO:0010115", "names": ["THORACIC DYSPLASIA-HYDROCEPHALUS SYNDROME", "thoracic dysplasia-hydrocephalus syndrome", "thoracic dysplasia hydrocephalus syndrome", "Thoracic Dysplasia-Hydrocephalus Syndrome", "Thoracic dysplasia-hydrocephalus syndrome", "Thoracic dysplasia and hydrocephalus syndrome", "Thoracic dysplasia and hydrocephalus syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thoracic dysplasia-hydrocephalus syndrome", "shortest_name_length": 41}
{"curie": "UMLS:C4287832", "names": ["Metastatic solid tumor", "Metastatic Solid Tumor", "Metastatic Solid Neoplasm", "Metastatic Malignant Solid Tumor", "Metastatic Malignant Solid Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Malignant Solid Neoplasm", "shortest_name_length": 22}
{"curie": "UMLS:C1832733", "names": ["Rhabdomyolysis, Cerivastatin-Induced"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rhabdomyolysis, Cerivastatin-Induced", "shortest_name_length": 36}
{"curie": "UMLS:C5239070", "names": ["Advanced Fibrosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Fibrosarcoma", "shortest_name_length": 21}
{"curie": "UMLS:C2063870", "names": ["Mucinous cystic tumor with moderate dysplasia", "mucinous cystic neoplasm with moderate dysplasia", "mucinous cystic neoplasm with moderate dysplasia (diagnosis)", "Pancreatic Mucinous-Cystic Neoplasm with Intermediate Grade Dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucinous cystic neoplasm with moderate dysplasia", "shortest_name_length": 45}
{"curie": "UMLS:C4525858", "names": ["Stage IV Colon Neuroendocrine Tumor", "Stage IV Colon Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Colon Neuroendocrine Tumor AJCC v8", "shortest_name_length": 35}
{"curie": "MONDO:0030700", "names": ["autoimmune glomerulonephritis", "autoimmune glomerulonephritis (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune glomerulonephritis", "shortest_name_length": 29}
{"curie": "MONDO:0017780", "names": ["Del(20)(p13)", "monosomy 20p13", "20p13 microdeletion syndrome", "20p subtelomeric deletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "20p13 microdeletion syndrome", "shortest_name_length": 12}
{"curie": "UMLS:C1710124", "names": ["Solid Angiomyoma", "Solid Angioleiomyoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Solid Angioleiomyoma", "shortest_name_length": 16}
{"curie": "MONDO:0005632", "names": ["ACS", "CHEST SYNDROME ACUTE", "Acute chest syndrome", "Acute Chest Syndrome", "acute chest syndrome", "Syndrome, Acute Chest", "Acute Chest Syndromes", "Syndromes, Acute Chest", "Acute chest syndrome (disorder)", "acute chest syndrome in sickle cell disease", "Acute chest syndrome in sickle cell disease", "acute chest syndrome in conditions classified elsewhere", "acute chest syndrome in conditions classified elsewhere (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute chest syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C3273240", "names": ["Pseudomonas-Related Vasculitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pseudomonas-Related Vasculitis", "shortest_name_length": 30}
{"curie": "UMLS:C5205119", "names": ["Advanced Lung Small Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Lung Small Cell Carcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0011954", "names": ["CMM4", "melanoma, cutaneous malignant, 4", "MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 4", "melanoma, cutaneous malignant, susceptibility to, 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melanoma, cutaneous malignant, susceptibility to, 4", "shortest_name_length": 4}
{"curie": "MONDO:0018023", "names": ["Hb-M disease", "M hemoglobinopathy", "blue baby syndrome", "Hemoglobin M Disease", "Hemoglobin M disease", "hemoglobin M disease", "Haemoglobin M disease", "Congenital methemoglobinemia", "METHEMOGLOBINEMIA, BETA TYPE", "methemoglobinemia, beta type", "Hereditary methemoglobinuria", "hereditary methemoglobinemia", "Hereditary methaemoglobinuria", "Hereditary M hemoglobinopathy", "Methemoglobinemia, hereditary", "hereditary; methemoglobinemia", "Hemoglobin M hemoglobinopathy", "methemoglobinemia; hereditary", "Hereditary M haemoglobinopathy", "Congenital methaemoglobinaemia", "methemoglobinemia; Hb-M disease", "hereditary hemoglobin M disease", "Hb-M disease; methemoglobinemia", "Hemoglobin M disease, hereditary", "hemoglobin M disease (diagnosis)", "Methemoglobinemia, Beta-Globin Type", "methemoglobinemia, beta-globin type", "autosomal dominant methemoglobinemia", "hereditary methemoglobinemia (diagnosis)", "disease (or disorder); hemoglobin or Hb, M", "hereditary hemoglobin M disease (diagnosis)", "hereditary methemoglobinemia due to hemoglobin mutation", "Hereditary methemoglobinemia due to globin chain mutation", "Hereditary methemoglobinaemia due to globin chain mutation", "Hereditary methemoglobinemia due to globin chain mutation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemoglobin M disease", "shortest_name_length": 12}
{"curie": "MONDO:0021580", "names": ["Jaw Neoplasm", "Jaw neoplasm", "Neoplasm, Jaw", "Jaw Neoplasms", "Neoplasms, Jaw", "neoplasm of jaw", "Neoplasm of jaw", "jaw skeleton tumor", "tumor of jaw skeleton", "jaw skeleton neoplasm", "neoplasm of jaw skeleton", "Neoplasm of jaw (disorder)", "neoplasm of jaw (diagnosis)", "jaw skeleton neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplasm of jaw", "shortest_name_length": 12}
{"curie": "MONDO:0017516", "names": ["short fingers, bilateral", "brachydactyly of fingers, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly of fingers, bilateral", "shortest_name_length": 24}
{"curie": "MONDO:0012906", "names": ["CILD9", "primary ciliary dyskinesia 9", "CILIARY DYSKINESIA, PRIMARY, 9", "ciliary dyskinesia, primary, 9", "Ciliary Dyskinesia, Primary, 9", "DNAI2 primary ciliary dyskinesia", "primary ciliary dyskinesia type 9", "ciliary dyskinesia, primary, type 9", "primary ciliary dyskinesia caused by mutation in DNAI2", "primary ciliary dyskinesia 9 with or without situs inversus", "Ciliary Dyskinesia, Primary, 9, With Or Without Situs Inversus", "ciliary dyskinesia, primary, 9, with or without situs inversus", "CILIARY DYSKINESIA, PRIMARY, 9, WITH OR WITHOUT SITUS INVERSUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia 9", "shortest_name_length": 5}
{"curie": "MONDO:0009945", "names": ["Epd", "PDE", "EPD", "pyridoxine dependency", "PYRIDOXINE DEPENDENCY", "antiquitin deficiency", "Antiquitin deficiency", "Pyridoxine dependency", "Vitamin B6-dependent seizures", "Aasa Dehydrogenase Deficiency", "AASA dehydrogenase deficiency", "pyridoxine-dependent epilepsy", "Pyridoxine-Dependent Seizures", "PYRIDOXINE-DEPENDENT EPILEPSY", "Pyridoxine-dependent epilepsy", "Vitamin B6-Dependent Seizures", "vitamin B6-dependent seizures", "AASA DEHYDROGENASE DEFICIENCY", "epilepsy pyridoxine dependent", "pyridoxine dependent epilepsy", "EPILEPSY, PYRIDOXINE-DEPENDENT", "Epilepsy, Pyridoxine-Dependent", "epilepsy, pyridoxine-dependent", "Pyridoxine dependency with seizures", "pyridoxine dependency with seizures", "PYRIDOXINE DEPENDENCY WITH SEIZURES", "Pyridoxine-dependent epilepsy (disorder)", "pyridoxine dependent epilepsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyridoxine-dependent epilepsy", "shortest_name_length": 3}
{"curie": "MONDO:0018533", "names": ["undifferentiated carcinoma of liver and IBT", "undifferentiated carcinoma of liver and intrahepatic biliary tract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "undifferentiated carcinoma of liver and intrahepatic biliary tract", "shortest_name_length": 43}
{"curie": "MONDO:0016393", "names": ["Bosma-Henkin-Christiansen syndrome", "Bosma arhinia-microphthalmia syndrome", "hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome", "shortest_name_length": 34}
{"curie": "UMLS:C0596298", "names": ["cerebral occlusion", "Occlusion;cerebral", "cerebral occlusions", "cerebrovascular occlusion", "Cerebrovascular Occlusion", "occlusion; cerebrovascular", "cerebrovascular; occlusion", "Occlusion, Cerebrovascular", "Cerebrovascular Occlusions", "Occlusions, Cerebrovascular"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebrovascular Occlusion", "shortest_name_length": 18}
{"curie": "UMLS:C5419617", "names": ["Advanced Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Non-Hodgkin Lymphoma", "shortest_name_length": 29}
{"curie": "MONDO:0006726", "names": ["Diaphragm Eventration", "diaphragm eventration", "eventration diaphragm", "DIAPHRAGM, EVENTRATION", "diaphragm; eventration", "eventration of diaphragm", "Eventration of Diaphragm", "Eventration of diaphragm", "Diaphragmatic eventration", "Diaphragmatic Eventration", "diaphragmatic eventration", "Eventration, Diaphragmatic", "Eventration of the diaphragm", "diaphragmatic eventration (disease)", "Diaphragmatic eventration (disorder)", "diaphragmatic eventration (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diaphragmatic eventration", "shortest_name_length": 21}
{"curie": "UMLS:C4525437", "names": ["Stage IIIB Ampulla of Vater Cancer", "Stage IIIB Ampulla of Vater Cancer AJCC v8", "Stage IIIB Ampulla of Vater Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Ampulla of Vater Cancer AJCC v8", "shortest_name_length": 34}
{"curie": "MONDO:0014414", "names": ["ADMIO", "ADMIO1", "Infantile-Onset Multisystem Autoimmune Disease 1", "autoimmune disease, multisystem, infantile-onset", "autoimmune disease, multisystem, infantile-onset, 1", "AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1", "STAT3-related early-onset multisystem autoimmune disease", "Signal transducer and activator of transcription 3-related early-onset multisystem autoimmune disease", "Signal transducer and activator of transcription 3-related early-onset multisystem autoimmune disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "STAT3-related early-onset multisystem autoimmune disease", "shortest_name_length": 5}
{"curie": "MONDO:0043116", "names": ["Iida Kannari syndrome", "Craniosynostosis with joint contractures, ear deformity, cleft palate, scoliosis, and other features", "craniosynostosis with joint contractures, ear deformity, cleft palate, scoliosis, and other features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Iida Kannari syndrome", "shortest_name_length": 21}
{"curie": "UMLS:C1257964", "names": ["Exogenous Hyperinsulinism", "exogenous hyperinsulinism", "Hyperinsulinism, Exogenous", "exogenous hyperinsulinism (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Exogenous Hyperinsulinism", "shortest_name_length": 25}
{"curie": "UMLS:C3899385", "names": ["Dialysis Catheter Exit Site Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dialysis Catheter Exit Site Infection", "shortest_name_length": 37}
{"curie": "MONDO:0008261", "names": ["Weary-Kindler syndrome", "hereditary sclerosing poikiloderma", "Hereditary sclerosing poikiloderma", "poikiloderma, hereditary sclerosing", "Poikiloderma, Hereditary Sclerosing", "POIKILODERMA, HEREDITARY SCLEROSING", "Hereditary sclerosing poikiloderma (disorder)", "hereditary sclerosing poikiloderma (diagnosis)", "hereditary sclerosing poikiloderma, Weary type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary sclerosing poikiloderma, Weary type", "shortest_name_length": 22}
{"curie": "MONDO:0054867", "names": ["paraomphalocele", "Paraomphalocele", "Paraomphalocele, epigastric", "Paraomphalocele, hypogastric"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paraomphalocele", "shortest_name_length": 15}
{"curie": "UMLS:C2063099", "names": ["Benign Ovarian Endometrioid Tumor", "benign endometrioid tumor of ovary", "benign endometrioid tumor of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign endometrioid tumor of ovary", "shortest_name_length": 33}
{"curie": "MONDO:0020088", "names": ["FPLD", "Dunnigan Syndrome", "Koberling Dunnigan Syndrome", "Koberling-Dunnigan syndrome", "Koberling-Dunnigan Syndrome", "Kobberling-Dunnigan syndrome", "Dunnigan-Kobberling syndrome", "genetic partial lipodystrophy", "Familial Partial Lipodystrophy", "Familial partial lipodystrophy", "familial partial lipodystrophy", "Partial Lipodystrophy, Familial", "lipodystrophy, familial partial", "Lipodystrophy, Familial Partial", "Congenital Partial Lipodystrophy", "Familial Partial Lipodystrophies", "congenital partial lipodystrophy", "Dunnigan-Kobberling syndrome (diagnosis)", "Familial partial lipodystrophy (disorder)", "Familial lipodystrophy of limbs and trunk", "Familial lipodystrophy of limbs AND/OR trunk"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial partial lipodystrophy", "shortest_name_length": 4}
{"curie": "MONDO:0030893", "names": ["LEPID", "LEUKOENCEPHALOPATHY, PROGRESSIVE, INFANTILE-ONSET, WITH OR WITHOUT DEAFNESS", "leukoencephalopathy, progressive, infantile-onset, with or without deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukoencephalopathy, progressive, infantile-onset, with or without deafness", "shortest_name_length": 5}
{"curie": "MONDO:0054764", "names": ["NBIA8", "neurodegeneration with brain iron accumulation 8", "NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodegeneration with brain iron accumulation 8", "shortest_name_length": 5}
{"curie": "MONDO:0011244", "names": ["MRSHSS", "Marshall-Smith syndrome", "MARSHALL-SMITH SYNDROME", "marshall smith syndrome", "marshall-smith syndrome", "Marshall-SMITH syndrome", "Marshall-Weaver syndrome", "Marshall-Smith syndrome (MSS)", "Marshall-Smith syndrome (disorder)", "accelerated skeletal maturation, Marshall-Smith type", "Accelerated skeletal maturation-facial dysmorphism-failure to thrive syndrome", "accelerated skeletal maturation-facial dysmorphism-failure to thrive syndrome", "Accelerated skeletal maturation, facial dysmorphism, failure to thrive syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Marshall-Smith syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0011101", "names": ["IRD", "PBD1B", "Mild PBD-ZSD", "Infantile Refsum disease", "Infantile Refsum Disease", "infantile refsum disease", "infantile Refsum disease", "Refsum disease, infantile", "REFSUM DISEASE, INFANTILE", "Infantile Refsums Disease", "Disease, Infantile Refsum", "Refsum Disease, Infantile", "Refsums Disease, Infantile", "infantile refsum's disease", "Infantile Refsum's Disease", "Infantile Refsum's disease", "Refsum's Disease, Infantile", "Disease, Infantile Refsum's", "Refsum Disease, Infantile Form", "peroxisome biogenesis disorder 1B", "PEROXISOME BIOGENESIS DISORDER 1B", "Peroxisome Biogenesis Disorder 1B", "infantile Refsum disease (diagnosis)", "Infantile Refsum's disease (disorder)", "peroxisome biogenesis disorder type 1B", "infantile phytanic acid storage disease", "INFANTILE PHYTANIC ACID STORAGE DISEASE", "Infantile Phytanic Acid Storage Disease", "ADRENOLEUKODYSTROPHY, AUTOSOMAL NEONATAL", "adrenoleukodystrophy, autosomal neonatal", "peroxisome biogenesis disorder (NALD/Ird)", "PEROXISOME BIOGENESIS DISORDER (NALD/IRD)", "peroxisome biogenesis disorder 1B (NALD/IRD)", "Infantile Form of Phytanic Acid Storage Disease", "Mild peroxisome biogenesis disorder-Zellweger spectrum disorder", "peroxisome biogenesis disorder (neonatal adrenoleukodystrophy/infantile Refsum disease)", "PEROXISOME BIOGENESIS DISORDER (NEONATAL ADRENOLEUKODYSTROPHY/INFANTILE REFSUM DISEASE)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder 1B", "shortest_name_length": 3}
{"curie": "UMLS:C2828032", "names": ["Stage IIC Skin Melanoma", "Stage IIC Skin Melanoma AJCC v7", "Stage IIC Skin Melanoma AJCC v6", "Stage IIC Cutaneous (Skin) Melanoma", "Stage IIC Cutaneous Melanoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIC Cutaneous Melanoma AJCC v6 and v7", "shortest_name_length": 23}
{"curie": "MONDO:0007543", "names": ["ENO4", "enolase, sperm specific"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "enolase, sperm specific", "shortest_name_length": 4}
{"curie": "UMLS:C0018984", "names": ["Hemicrania Migraine", "Hemicrania migraine", "hemicrania; migraine", "Migraine, Hemicrania", "migraine; hemicrania", "Hemicrania Migraines", "Migraines, Hemicrania"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemicrania migraine", "shortest_name_length": 19}
{"curie": "MONDO:0017453", "names": ["fifth disease", "Fetal parvovirus syndrome", "fetal parvovirus syndrome", "Foetal parvovirus syndrome", "Parvovirus antenatal infection", "Parvovirus B19 antenatal infection", "Maternofetal infection by parvovirus", "Fetal parvovirus syndrome (disorder)", "Human parvovirus B19 infectious embryofetopathy", "mother-to-child transmission of parvovirus syndrome", "Mother-to-child transmission of parvovirus syndrome", "Human parvovirus B19 caused infectious embryofetopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fetal parvovirus syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0010428", "names": ["Dup(X)(p11.22p11.23)", "Trisomy Xp11.22p11.23", "trisomy Xp11.22-p11.23", "Trisomy Xp11.22-p11.23", "Xp11.22-p11.23 Microduplication", "Microduplication Xp11.22p11.23 syndrome", "microduplication Xp11.22-p11.23 syndrome", "Chromosome Xp11.23-P11.22 Duplication Syndrome", "CHROMOSOME Xp11.23-p11.22 DUPLICATION SYNDROME", "chromosome Xp11.23-p11.22 duplication syndrome", "Microduplication Xp11.22p11.23 syndrome (disorder)", "chromosome xp11.23-p11.22 duplication syndrome, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome Xp11.23-p11.22 duplication syndrome", "shortest_name_length": 20}
{"curie": "EFO:1002004", "names": ["drug hypersensitivity syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "drug hypersensitivity syndrome", "shortest_name_length": 30}
{"curie": "MONDO:0008156", "names": ["OPTA2", "Albers-Schönberg osteopetrosis", "Albers Schonberg osteopetrosis", "Albers-Schonberg osteopetrosis", "marble bones, autosomal dominant", "MARBLE BONES, AUTOSOMAL DOMINANT", "Marble Bones, Autosomal Dominant", "autosomal dominant osteopetrosis 2", "Osteopetrosis, Autosomal Dominant 2", "osteopetrosis, autosomal dominant 2", "OSTEOPETROSIS, AUTOSOMAL DOMINANT 2", "OSTEOSCLEROSIS FRAGILIS GENERALISATA", "osteosclerosis Fragilis generalisata", "Autosomal Dominant Osteopetrosis Type 2", "Osteopetrosis Autosomal Dominant Type 2", "Osteopetrosis autosomal dominant type 2", "Autosomal dominant osteopetrosis type 2", "autosomal dominant osteopetrosis type 2", "osteopetrosis autosomal dominant type 2", "osteopetrosis, autosomal dominant type 2", "autosomal dominant osteopetrosis type II", "osteopetrosis, autosomal dominant, type 2", "Osteopetrosis, Autosomal Dominant, Type II", "OSTEOPETROSIS, AUTOSOMAL DOMINANT, TYPE II", "autosomal dominant Albers-Schonberg disease", "Albers-Schonberg Disease, Autosomal Dominant", "Albers Schonberg Disease, Autosomal Dominant", "ALBERS-SCHONBERG DISEASE, AUTOSOMAL DOMINANT", "Albers-Schonberg disease, autosomal dominant", "Autosomal dominant osteopetrosis type 2 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant osteopetrosis 2", "shortest_name_length": 5}
{"curie": "MONDO:0060496", "names": ["CMND", "NEDHND", "MYOPATHY, CONGENITAL, WITH NEUROPATHY AND DEAFNESS", "myopathy, Congenital, with neuropathy and Deafness", "NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, NEUROPATHY, AND DEAFNESS", "neurodevelopmental disorder with hypotonia, neuropathy, and deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with hypotonia, neuropathy, and deafness", "shortest_name_length": 4}
{"curie": "UMLS:C0271387", "names": ["rebound nystagmus", "Rebound nystagmus", "Rebound Nystagmus", "Nystagmus, rebound", "Nystagmus, Rebound", "Rebound nystagmus (disorder)", "rebound nystagmus was observed", "rebound nystagmus (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rebound Nystagmus", "shortest_name_length": 17}
{"curie": "UMLS:C0262534", "names": ["labile htn", "labile hypertension", "White Coat Syndrome", "Syndrome, White Coat", "White Coat Hypertension", "White coat hypertension", "Hypertension;white coat", "white coat hypertension", "coat hypertension white", "hypertension white coat", "Hypertension, White Coat", "Isolated Clinic Hypertension", "Hypertension, Isolated Clinic", "Clinic Hypertension, Isolated", "Labile hypertension due to being in a clinical environment", "Labile hypertension due to being in a clinical environment (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "White Coat Hypertension", "shortest_name_length": 10}
{"curie": "UMLS:C1332470", "names": ["Benign Ameloblastoma", "AMELOBLASTOMA, BENIGN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Ameloblastoma", "shortest_name_length": 20}
{"curie": "MONDO:0009090", "names": ["autosomal-mitochondrial sensorineural deafness", "DEAFNESS, SENSORINEURAL, AUTOSOMAL-MITOCHONDRIAL TYPE", "Deafness, Sensorineural, Autosomal-Mitochondrial Type", "deafness, sensorineural, autosomal-mitochondrial type", "hearing loss, sensorineural, autosomal-mitochondrial type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, sensorineural, autosomal-mitochondrial type", "shortest_name_length": 46}
{"curie": "UMLS:C1707541", "names": ["Cutaneous Angioimmunoblastic T-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous Angioimmunoblastic T-Cell Lymphoma", "shortest_name_length": 44}
{"curie": "UMLS:C2984098", "names": ["Penile Cancer by AJCC v7 Stage", "Penile Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Penile Cancer by AJCC v7 Stage", "shortest_name_length": 30}
{"curie": "MONDO:0019177", "names": ["Odontoleukodystrophy", "odontoleukodystrophy", "dentoleukoencephalopathy", "Dentoleukoencephalopathy", "Leukodystrophy with oligodontia", "Leucodystrophy with oligodontia", "Odontoleukodystrophy (disorder)", "leukodystrophy with oligodontia", "Leukodystrophy, Dysmyelinating, with Oligodontia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "odontoleukodystrophy", "shortest_name_length": 20}
{"curie": "MONDO:0019723", "names": ["basement membrane disease", "disease of glomerular basement membrane"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disease of glomerular basement membrane", "shortest_name_length": 25}
{"curie": "MONDO:0018948", "names": ["MmD", "multicore", "Minicore disease", "multicore disease", "Multicore disease", "Multi-core disease", "multicore myopathy", "disease; multicore", "Multicore myopathy", "multiminicore disease", "Multiminicore disease", "Multiminicore myopathy", "congenital myopathy 1B", "Multi-minicore disease", "multiminicore myopathy", "Multi-core congenital myopathy", "disease (or disorder); multicore", "Multi-core congenital myopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiminicore myopathy", "shortest_name_length": 3}
{"curie": "MONDO:0019690", "names": ["bone filaminopathy", "filamin-related bone disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "filamin-related bone disorder", "shortest_name_length": 18}
{"curie": "MONDO:0004234", "names": ["CNKL", "CLPD-NK", "NK-LGLL", "NK-LGL leukemia", "chronic NK lymphocytosis", "Chronic NK lymphocytosis", "Chronic NK-Cell Lymphocytosis", "Chronic NK-cell lymphocytosis", "chronic NK-cell lymphocytosis", "chronic NK-LGL lymphoproliferative disorder", "Chronic NK-LGL Lymphoproliferative Disorder", "Indolent NK-Cell Lymphoproliferative Disorder", "indolent NK-cell lymphoproliferative disorder", "NK-cell large granular Lymphocyte Lymphocytosis", "NK-Cell Large Granular Lymphocyte Lymphocytosis", "NK-cell large granular lymphocyte lymphocytosis", "Chronic lymphoproliferative disorder of NK cells", "Chronic Lymphoproliferative Disorder of NK-Cells", "chronic lymphoproliferative disorder of NK cells", "Chronic lymphoproliferative disorder of NK-cells", "chronic lymphoproliferative disorder of NK-cells", "natural killer-cell large granular lymphocyte leukemia", "NK-cell lineage granular lymphocyte proliferative disorder", "chronic lymphoproliferative disorder of natural killer cells", "NK-Type Lymphoproliferative Disorder of Granular Lymphocytes", "Indolent Large Granular NK-Cell Lymphoproliferative Disorder", "Chronic lymphoproliferative disorder of natural killer cells", "NK-type lymphoproliferative disorder of granular lymphocytes", "indolent large granular NK-cell lymphoproliferative disorder", "chronic NK-large granular lymphocyte lymphoproliferative disorder", "Chronic NK-Large Granular Lymphocyte Lymphoproliferative Disorder", "Chronic lymphoproliferative disorder of natural killer cells (disorder)", "Chronic lymphoproliferative disorder of natural killer cells (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic lymphoproliferative disorder of NK-cells", "shortest_name_length": 4}
{"curie": "UMLS:C5203824", "names": ["Borderline Serous Cystadenofibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Serous Cystadenofibroma", "shortest_name_length": 34}
{"curie": "UMLS:C5447361", "names": ["Quantitative defects", "Immunodeficiency due to Quantitative Defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immunodeficiency due to Quantitative Defects", "shortest_name_length": 20}
{"curie": "UMLS:C0344487", "names": ["Lateral meningocele", "lateral meningocele", "lateral meningoceles", "Lateral meningocele (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lateral meningocele", "shortest_name_length": 19}
{"curie": "UMLS:C5239129", "names": ["Peritoneal Sarcomatoid Mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peritoneal Sarcomatoid Mesothelioma", "shortest_name_length": 35}
{"curie": "MONDO:0023155", "names": ["fibula aplasia complex brachydactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibula aplasia complex brachydactyly", "shortest_name_length": 36}
{"curie": "MONDO:0012698", "names": ["WS2E", "Waardenburg syndrome type 2E", "WAARDENBURG SYNDROME, TYPE 2E", "Waardenburg syndrome type IIE", "Waardenburg Syndrome, Type 2E", "Waardenburg syndrome, type 2E", "Waardenburg Syndrome, Type IIE", "WAARDENBURG SYNDROME, TYPE IIE", "SOX10 Waardenburg syndrome type 2", "WS2E, WITH OR WITHOUT NEUROLOGIC INVOLVEMENT", "Ws2E, with or without neurologic involvement", "WS2E with or without neurological involvement", "Waardenburg syndrome type 2 caused by mutation in SOX10", "Waardenburg syndrome type 2E with or without neurologic involvement", "Waardenburg Syndrome, Type 2E, With Or Without Neurologic Involvement", "Waardenburg syndrome, type 2E, with or without neurologic involvement", "WAARDENBURG SYNDROME, TYPE 2E, WITH OR WITHOUT NEUROLOGIC INVOLVEMENT", "hypogonadotropic hypogonadism with anosmia and deafness with or without hypopigmentation", "hypogonadotropic hypogonadism with anosmia and deafness, with or without hypopigmentation", "HYPOGONADOTROPIC HYPOGONADISM WITH ANOSMIA AND DEAFNESS, WITH OR WITHOUT HYPOPIGMENTATION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Waardenburg syndrome type 2E", "shortest_name_length": 4}
{"curie": "MONDO:0008597", "names": ["TRPS3", "TRPS 3", "Sugio-Kajii syndrome", "SUGIO-KAJII SYNDROME", "Sugio-Kajii Syndrome", "trichorhinophalangeal syndrome type 3", "trichorhinophalangeal syndrome, type 3", "trichorhinophalangeal syndrome type III", "Trichorhinophalangeal Syndrome, Type III", "TRICHORHINOPHALANGEAL SYNDROME, TYPE III", "trichorhinophalangeal syndrome, type III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichorhinophalangeal syndrome, type III", "shortest_name_length": 5}
{"curie": "UMLS:C1328395", "names": ["Vaginal contraceptive device expelled"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal contraceptive device expelled", "shortest_name_length": 37}
{"curie": "MONDO:0015909", "names": ["Anemia aplastic", "aplastic anemia", "APLASTIC ANEMIA", "Aplastic anemia", "ANEMIA APLASTIC", "Aplastic Anemia", "Anaemia aplastic", "Anemia, Aplastic", "Aplastic anaemia", "aplastic anaemia", "anemia; aplastic", "Aplastic Anaemia", "ANEMIA, APLASTIC", "Aplastic Anemias", "ANAEMIA APLASTIC", "Anaemia;aplastic", "aplastic; anemia", "erythroid aplasia", "Anaemia, Aplastic", "Erythroid aplasia", "Aplastic Anaemias", "Aplastic anemia NOS", "bone marrow aplasia", "aplastic anemia nos", "Aregenerative anemia", "Aplastic anemia, NOS", "Aplastic anaemia, NOS", "Aregenerative anaemia", "Hematopoietic aplasia", "Haematopoietic aplasia", "Non regenerative anemia", "Non regenerative anaemia", "Aplastic anemia (disorder)", "aplastic anemia (diagnosis)", "Aplastic anemia, unspecified", "Aplastic anaemia, unspecified", "Hematopoietic aplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aplastic anemia", "shortest_name_length": 15}
{"curie": "MONDO:0006590", "names": ["Palmoplantar Keratoses", "Palmoplantar Keratosis", "palmoplantar keratosis", "Keratosis, Palmoplantar", "Keratoses, Palmoplantar", "palmoplantar keratoderma", "Palmoplantar keratoderma", "Palmoplantar Keratoderma", "keratoderma palmoplantar", "Keratoderma, Palmoplantar", "palmoplantar keratodermas", "keratoderma, palmoplantar", "Palmoplantar Keratodermas", "palmo-plantar keratodermas", "Keratodermas, Palmoplantar", "Thickening of palms and soles", "Palmar and plantar keratoderma", "Keratosis palmaris et plantaris", "Keratosis Palmaris et Plantaris", "keratosis palmaris et plantaris", "et keratoderma palmaris plantaris", "Hyperkeratosis of palms and soles", "Keratoderma palmaris et plantaris", "Palmoplantar keratoderma (disorder)", "Hyperkeratosis Palmaris et Plantaris", "palmoplantar keratoderma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "palmoplantar keratosis", "shortest_name_length": 22}
{"curie": "UMLS:C4329675", "names": ["Stage III HPV-Mediated (p16-Positive) Oropharyngeal Throat Cancer", "Clinical Stage III HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage III HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8", "shortest_name_length": 65}
{"curie": "MONDO:0017426", "names": ["Extra pinky finger", "Extra pinkie finger", "Extra little finger", "Accessory little finger", "Postaxial hand polydactyly", "postaxial polydactyly hands", "Ulnar polydactyly of fingers", "postaxial polydactyly of hand", "Postaxial polydactyly of hand", "postaxial polydactyly of hands", "Postaxial polydactyly of hands", "postaxial polydactyly of fingers", "Postaxial polydactyly of fingers", "Polydactyly affecting the 5th finger", "Ulnar polydactyly of fingers (disorder)", "postaxial polydactyly hands (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postaxial polydactyly of fingers", "shortest_name_length": 18}
{"curie": "MONDO:0015579", "names": ["Bart's disease", "Alpha-thalassemia major", "Alpha thalassemia major", "alpha thalassemia major", "Alpha thalassaemia major", "Hemoglobin Barts hydrops", "Hemoglobin Bart's disease", "Hb Bart's hydrops fetalis", "Haemoglobin Barts hydrops", "Bart's disease (diagnosis)", "Haemoglobin Bart's disease", "Homozygous alpha0-thalassemia", "homozygous alpha0-thalassemia", "Hemoglobin Bart hydrops syndrome", "Haemoglobin Bart hydrops syndrome", "Hemoglobin Bart's hydrops fetalis", "Alpha-thalassemia hydrops fetalis", "Hemoglobin Bart's hydrops syndrome", "Haemoglobin Bart's hydrops syndrome", "alpha thalassemia major (diagnosis)", "Hemoglobin Bart's hydrops syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hb Bart's hydrops fetalis", "shortest_name_length": 14}
{"curie": "MONDO:0013656", "names": ["MRD9", "NESCAVS", "MRD9, FORMERLY", "NESCAV syndrome", "NESCAV SYNDROME", "autosomal dominant mental retardation 9", "mental retardation, autosomal dominant 9", "Mental Retardation, Autosomal Dominant 9", "autosomal dominant intellectual disability 9", "mental retardation, autosomal dominant type 9", "intellectual disability, autosomal dominant 9", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 9, FORMERLY", "intellectual disability, autosomal dominant type 9", "autosomal dominant non-syndromic intellectual disability 9", "KIF1A autosomal dominant non-syndromic intellectual disability", "autosomal dominant non-syndromic intellectual disability caused by mutation in KIF1A", "NEURODEGENERATION AND SPASTICITY WITH OR WITHOUT CEREBELLAR ATROPHY OR CORTICAL VISUAL IMPAIRMENT", "neurodegeneration and spasticity with or without cerebellar atrophy or cortical visual impairment"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 9", "shortest_name_length": 4}
{"curie": "UMLS:C4525343", "names": ["Hilar Cholangiocarcinoma by AJCC v8 Stage", "Perihilar Cholangiocarcinoma by AJCC v8 Stage", "Hilar Cholangiocarcinoma Tumor Stage (Pathologic)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hilar Cholangiocarcinoma by AJCC v8 Stage", "shortest_name_length": 41}
{"curie": "UMLS:C5418882", "names": ["Advanced Carcinosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Carcinosarcoma", "shortest_name_length": 23}
{"curie": "MONDO:0010077", "names": ["Smed-SL", "SMED-SL", "SMED-SL/AC", "Smed-SL/Ac", "SMED type 2", "SMED Type II", "Smed, type 2", "SMED, TYPE II", "SMED, type II", "SMED short limb-hand type", "Smed, short limb-hand type", "SMED, SHORT LIMB-HAND TYPE", "SMED, Short Limb-Hand Type", "SMED short limb-abnormal calcification type", "Smed short limb-abnormal calcification type", "SMED, SHORT LIMB-ABNORMAL CALCIFICATION TYPE", "Smed, short limb-abnormal calcification type", "SMED, Short Limb-Abnormal Calcification Type", "spondylometaepiphyseal dysplasia short limb-hand type", "spondylometaepiphyseal dysplasia, short limb-hand type", "Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type", "SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE", "spondyloepimetaphyseal dysplasia - short limb - abnormal calcification", "spondylometaepiphyseal dysplasia short limb-abnormal calcification type", "Spondylometaepiphyseal Dysplasia, Short Limb-Abnormal Calcification Type", "SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-ABNORMAL CALCIFICATION TYPE", "spondylometaepiphyseal dysplasia, short limb-abnormal calcification type", "spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome", "shortest_name_length": 7}
{"curie": "MONDO:0016333", "names": ["DCM", "Familial dilated cardiomyopathy", "familial dilated cardiomyopathy", "cardiomyopathy dilated familial", "cardiomyopathy, familial dilated", "dilated cardiomyopathy, familial", "hereditary dilated cardiomyopathy", "idiopathic dilated cardiomyopathy", "cardiomyopathy, familial dilated, 1", "Primary familial dilated cardiomyopathy", "Familial dilated cardiomyopathy (diagnosis)", "hypokinetic dilated cardiomyopathy, familial", "Primary familial dilated cardiomyopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial dilated cardiomyopathy", "shortest_name_length": 3}
{"curie": "MONDO:0011006", "names": ["SPG9A", "AD-SPG9A", "hereditary spastic paraplegia 9A", "hereditary spastic paraplegia type 9A", "Autosomal dominant spastic paraparesis", "autosomal dominant spastic paraplegia 9A", "Spastic paraplegia 9, autosomal dominant", "spastic paraplegia 9A, autosomal dominant", "SPASTIC PARAPLEGIA 9A, AUTOSOMAL DOMINANT", "Autosomal dominant spastic paraplegia type 9A", "autosomal dominant spastic paraplegia type 9A", "autosomal dominant complex spastic paraplegia type 9A", "Autosomal dominant spastic paraplegia type 9A (disorder)", "autosomal dominant spastic paraplegia type 9A (diagnosis)", "cataracts motor neuropathy-short stature-skeletal anomalies syndrome", "Cataracts motor neuropathy-short stature-skeletal anomalies syndrome", "Cataracts-motor neuropathy-short stature-skeletal anomalies syndrome", "Cataracts, motor neuropathy, short stature, skeletal anomalies syndrome", "Cataracts, motor neuronopathy, short stature and skeletal abnormalities", "Spastic paraparesis-amyopathy-cataracts-gastroesophageal reflux syndrome", "spastic paraparesis-amyopathy-cataracts-gastroesophageal reflux syndrome", "spastic paraparesis with amyopathy, cataracts and gastroesophageal reflux", "Spastic Paraparesis With Amyopathy, Cataracts, And Gastroesophageal Reflux", "spastic paraparesis with amyopathy, cataracts, and gastroesophageal reflux", "SPASTIC PARAPARESIS WITH AMYOTROPHY, CATARACTS, AND GASTROESOPHAGEAL REFLUX", "cataracts with motor neuronopathy, short stature and skeletal abnormalities", "spastic paraparesis with amyotrophy, cataracts, and gastroesophageal reflux", "cataracts with motor neuronopathy, short stature, and skeletal abnormalities", "CATARACTS WITH MOTOR NEURONOPATHY, SHORT STATURE, AND SKELETAL ABNORMALITIES", "Spastic paraparesis, amyotrophy, cataracts, gastroesophageal reflux syndrome", "Cataracts With Motor Neuronopathy, Short Stature, And Skeletal Abnormalities", "Spastic paraparesis, amyotrophy, cataracts, gastro-oesophageal reflux syndrome", "Bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 9A", "shortest_name_length": 5}
{"curie": "UMLS:C4723838", "names": ["Metastatic Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Breast Carcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0030813", "names": ["IMD101", "immunodeficiency 101 (varicella zoster virus-specific)", "IMMUNODEFICIENCY 101 (VARICELLA ZOSTER VIRUS-SPECIFIC)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 101 (varicella zoster virus-specific)", "shortest_name_length": 6}
{"curie": "MONDO:0009582", "names": ["Mietens", "Mietens syndrome", "Mietens' syndrome", "MIETENS-WEBER SYNDROME", "Mietens-Weber syndrome", "Mietens syndrome (disorder)", "Mental retardation Mietens Weber type", "intellectual disability, Mietens-Weber type", "Intellectual disability, Mietens-Weber type", "Mental retardation syndrome, Mietens Weber type", "mental retardation syndrome, Mietens-WEBER type", "mental retardation syndrome, Mietens Weber type", "MENTAL RETARDATION SYNDROME, MIETENS-WEBER TYPE", "Mental Retardation Syndrome, Mietens-Weber Type", "intellectual disability syndrome, Mietens-WEBER type", "intellectual disability syndrome, Mietens Weber type", "corneal opacity, nystagmus, flexion contracture of the elbows, growth failure, and mental retardation", "corneal opacity, nystagmus, flexion contracture of the elbows, growth failure, and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mietens syndrome", "shortest_name_length": 7}
{"curie": "MONDO:0016277", "names": ["mixed epithelial and mesenchymal cancer of cervix uteri", "cervical malignant mixed epithelial and mesenchymal tumor", "malignant mixed epithelial and mesenchymal tumor of cervix uteri"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant mixed epithelial and mesenchymal tumor of cervix uteri", "shortest_name_length": 55}
{"curie": "UMLS:C3272421", "names": ["Malignant Gastric Gastrointestinal Stromal Tumor", "Gastric Malignant Gastrointestinal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Malignant Gastrointestinal Stromal Tumor", "shortest_name_length": 48}
{"curie": "UMLS:C5206783", "names": ["Normal Karyotype Intermediate Risk Acute Myeloid Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Normal Karyotype Intermediate Risk Acute Myeloid Leukemia", "shortest_name_length": 57}
{"curie": "MONDO:0005439", "names": ["type II hyperlipidemia", "Type II Hyperlipidemia", "hyperbetalipoproteinemia", "familial hypercholesteremia", "hyperlipoproteinemia type II", "Hyperlipoproteinemia, Type II", "familial hypercholesterolemia", "Fredrickson type IIa lipidaemia", "familial hyperbetalipoproteinaemia", "Fredrickson type IIa hyperlipoproteinemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial hypercholesterolemia", "shortest_name_length": 22}
{"curie": "MONDO:0005008", "names": ["Colorectal Adenocarcinoma", "colorectum adenocarcinoma", "colorectal adenocarcinoma", "Colorectal adenocarcinoma", "adenocarcinomas colorectal", "Large Bowel Adenocarcinoma", "large bowel adenocarcinoma", "adenocarcinoma of large bowel", "Adenocarcinoma of Large Bowel", "large intestine adenocarcinoma", "Large Intestine Adenocarcinoma", "adenocarcinoma of large intestine", "Adenocarcinoma of Large Intestine", "adenocarcinoma of the large bowel", "Adenocarcinoma of large intestine", "Adenocarcinoma of the Large Bowel", "Adenocarcinoma of the Large Intestine", "adenocarcinoma of the large intestine", "Adenocarcinoma of the large intestine", "colorectal (colon or rectal) adenocarcinoma", "Colorectal (Colon or Rectal) Adenocarcinoma", "Adenocarcinoma of large intestine (disorder)", "adenocarcinoma of large intestine (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorectal adenocarcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0001528", "names": ["Ca vulva", "Vulval Ca", "Vulva Cancer", "Vulvar tumor", "cancer vulva", "vulva cancer", "Cancer, Vulva", "Vulval cancer", "vulval cancer", "vulvar cancer", "Vulvar cancer", "cancer vulvar", "VULVAR CANCER", "Vulvar Cancer", "Vulva Cancers", "Vulva--Cancer", "Vulvar Cancers", "Cancer, Vulvar", "Cancers, Vulva", "Cancer of vulva", "Cancers, Vulvar", "vulval neoplasm", "vulvar neoplasm", "of vulva cancer", "Cancer of Vulva", "cancer of vulva", "Vulvar Neoplasms", "neoplasm of vulva", "Vulval cancer NOS", "cancer of the vulva", "Cancer of the Vulva", "Malignant Vulva Tumor", "malignant vulva tumor", "Malignant Vulvar Tumor", "mammalian vulva cancer", "malignant vulvar tumor", "malignant Vulvar tumor", "malignant tumor of vulva", "Malignant tumor of vulva", "malignant vulva neoplasm", "Malignant Vulva Neoplasm", "Malignant Tumor of Vulva", "vulvar neoplasm malignant", "cancer of mammalian vulva", "Malignant Vulvar Neoplasm", "malignant vulvar neoplasm", "Malignant tumour of vulva", "Malignant neoplasm of vulva", "Malignant Neoplasm of Vulva", "malignant neoplasm of vulva", "Malignant Tumor of the Vulva", "malignant tumor of the vulva", "Malignant Neoplasm of the Vulva", "malignant neoplasm of the vulva", "Malignant neoplasm of vulva, NOS", "malignant mammalian vulva neoplasm", "Malignant tumor of vulva (disorder)", "malignant neoplasm of mammalian vulva", "malignant neoplasm of vulva unspecified", "malignant neoplasm of vulva (diagnosis)", "malignant neoplasm of vulva, unspecified", "Malignant neoplasm of vulva, unspecified", "Malignant neoplasm of vulva, unspecified site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulva cancer", "shortest_name_length": 8}
{"curie": "MONDO:0006160", "names": ["colorectal hamartoma", "Colorectal Hamartoma", "Large Intestinal Hamartoma", "large intestinal hamartoma", "colorectum hamartoma (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorectal hamartoma", "shortest_name_length": 20}
{"curie": "UMLS:C3698308", "names": ["Acquired Urinary Tract Obstruction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired Urinary Tract Obstruction", "shortest_name_length": 34}
{"curie": "MONDO:0010518", "names": ["WAS", "Imd2", "WAS1", "IMD2", "Imd 2", "Aldrich", "Wiskott-Aldrich", "Aldrich Syndrome", "Wiskott syndrome", "aldrich syndrome", "wiskott syndrome", "Aldrich syndrome", "Wiskott Syndrome", "ALDRICH SYNDROME", "Wiskott Syndromes", "Immunodeficiency 2", "immunodeficiency 2", "IMMUNODEFICIENCY 2", "Immunodeficiency 2s", "Wiskott Aldrich Syndrome", "Wiskott Aldrich syndrome", "Wiskott-Aldrich Syndrome", "WISKOTT-ALDRICH SYNDROME", "wiskott aldrich syndrome", "wiskott-aldrich syndrome", "aldrich syndrome wiskott", "Wiskott-aldrich syndrome", "Wiskott-Aldrich syndrome", "Wiskott-Aldrich syndrome 1", "WISKOTT-ALDRICH SYNDROME 1", "WAS - Wiskott-Aldrich syndrome", "eczema thromocytopenia syndrome", "familial; eczema-thrombocytopenia", "Wiskott-Aldrich syndrome (disorder)", "Wiskott-Aldrich syndrome (diagnosis)", "eczema thromocytopenia diarrhea syndrome", "thrombocytopenia; eczema, immunodeficiency", "Wiskott-Aldrich syndrome, X-linked recessive", "immunodeficiency; thrombocytopenia and eczema", "eczema thromocytopenia immunodeficiency syndrome", "IMMUNODEFICIENCY WITH ECZEMA AND THROMBOCYTOPENIA", "eczema-thrombocytopenia-immunodeficiency syndrome", "Eczema Thrombocytopenia Immunodeficiency Syndrome", "Immunodeficiency with thrombocytopenia AND eczema", "Eczema-Thrombocytopenia-Immunodeficiency Syndrome", "ECZEMA-THROMBOCYTOPENIA-IMMUNODEFICIENCY SYNDROME", "Immunodeficiency with thrombocytopenia and eczema", "eczema thrombocytopenia immunodeficiency syndrome", "Eczema-thrombocytopenia-immunodeficiency syndrome", "Eczema-Thrombocytopenia-Immunodeficiency Syndromes", "Eczema, thrombocytopenia, immunodeficiency syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wiskott-Aldrich syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0008653", "names": ["VUR", "VUR1", "Vesicoureteral reflux", "Vesicoureteral Reflux1", "Reflux1, Vesicoureteral", "Vesicoureteral Reflux1s", "Vesicoureteral Reflux 1", "vesicoureteral reflux 1", "VESICOURETERAL REFLUX 1", "Vesicoureteral Reflux Grade1", "Grade1, Vesicoureteral Reflux"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vesicoureteral reflux 1", "shortest_name_length": 3}
{"curie": "MONDO:0100024", "names": ["self-limited familial infantile epilepsy", "self-limited familial and non-familial infantile seizures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "self-limited familial infantile epilepsy", "shortest_name_length": 40}
{"curie": "MONDO:0015496", "names": ["MACROGLOSSIA", "large tongue", "Macroglossia", "Large tongue", "giant tongue", "macroglossia", "Macroglossias", "large tongues", "Tongue enlarged", "enlarged tongue", "Tongue Enlarged", "ENLARGED TONGUE", "Enlarged tongue", "Tongue hypertrophy", "tongue enlargement", "tongue hypertrophy", "Lingual hypertrophy", "tongue; hypertrophy", "tongue; enlargement", "Lingual hyperplasia", "hypertrophy; tongue", "Glossal hypertrophy", "enlargement; tongue", "hypertrophy of tongue", "Hypertrophy of tongue", "Enlargement of tongue", "Abnormally large tongue", "Increased size of tongue", "Hyperplasia of the tongue", "Hypertrophy of the tongue", "macroglossia (physical finding)", "Enlargement of tongue (disorder)", "hypertrophy of tongue (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macroglossia", "shortest_name_length": 12}
{"curie": "MONDO:0000342", "names": ["Onyong-nyong fever", "O'nyong-nyong fever", "O'nyong'nyong fever", "O'Nyong-Nyong fever", "fever; O'nyong-nyong", "O'nyong-nyong; fever", "ONN - O'nyong-nyong fever", "O'nyong-nyong fever (disorder)", "O'Nyong-Nyong fever (diagnosis)", "arthritis; O'nyong-nyong (etiology)", "O'nyong-nyong; arthritis (etiology)", "O'nyong-nyong virus infectious disease", "O'nyong-nyong virus disease or disorder", "O'nyong-nyong; arthritis (manifestation)", "arthritis; O'nyong-nyong (manifestation)", "Mosquito-borne viral fever, O'Nyong-Nyong", "O'nyong-nyong virus caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "O'nyong'nyong fever", "shortest_name_length": 18}
{"curie": "UMLS:C2721675", "names": ["Posterior Fossa Syndrome", "Posterior fossa syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Posterior fossa syndrome", "shortest_name_length": 24}
{"curie": "UMLS:C5208244", "names": ["Immune-mediated nephritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immune-mediated nephritis", "shortest_name_length": 25}
{"curie": "MONDO:0000589", "names": ["musculoskeletal system autoimmune disease", "autoimmune disease of musculoskeletal system", "autoimmune disorder of musculoskeletal system", "musculoskeletal system hypersensitivity reaction type II disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune disorder of musculoskeletal system", "shortest_name_length": 41}
{"curie": "MONDO:0017483", "names": ["humeral agenesis/hypoplasia, bilateral", "humeral intercalary meromelia, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "humeral agenesis/hypoplasia, bilateral", "shortest_name_length": 38}
{"curie": "UMLS:C0740399", "names": ["Audiovisual hallucinations", "audio visual hallucinations", "HALLUCINATION VISUAL AUDITORY", "visual auditory hallucinations", "Audio and visual hallucinations", "auditory and visual hallucinations", "Auditory and visual hallucinations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Audio and visual hallucinations", "shortest_name_length": 26}
{"curie": "MONDO:0011497", "names": ["NAIC", "North American Indian Childhood Cirrhosis", "North American Indian childhood cirrhosis", "NORTH AMERICAN INDIAN CHILDHOOD CIRRHOSIS", "NORTH American Indian childhood cirrhosis", "NAIC - North American Indian childhood cirrhosis", "Hereditary North American Indian childhood cirrhosis", "North American Indian childhood cirrhosis (disorder)", "hereditary North American Indian childhood cirrhosis", "North American Indian childhood cirrhosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary North American Indian childhood cirrhosis", "shortest_name_length": 4}
{"curie": "MONDO:0014088", "names": ["FASPS2", "advanced sleep phase syndrome 2", "CSNK1D advanced sleep phase syndrome", "advanced sleep phase syndrome type 2", "familial advanced sleep phase syndrome 2", "advanced sleep-phase syndrome, familial, 2", "ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 2", "advanced sleep phase syndrome, familial, 2", "advanced sleep phase syndrome, familial, type 2", "advanced sleep phase syndrome caused by mutation in CSNK1D"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "advanced sleep phase syndrome 2", "shortest_name_length": 6}
{"curie": "UMLS:C1711182", "names": ["Small Intestinal Adenosquamous Cancer", "Small Intestinal Adenosquamous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Intestinal Adenosquamous Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0016638", "names": ["familial hypodysfibrinogenemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial hypodysfibrinogenemia", "shortest_name_length": 30}
{"curie": "UMLS:C0341253", "names": ["Brunner gland hyperplasia", "Brunner's gland hyperplasia", "Brunner's Gland Hyperplasia", "Hyperplasia of Brunner glands of duodenum", "Hyperplasia of Brunner glands of duodenum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyperplasia of Brunner glands of duodenum", "shortest_name_length": 25}
{"curie": "UMLS:C4745261", "names": ["Invasive Follicular Variant Thyroid Gland Papillary Carcinoma", "Follicular Variant Thyroid Gland Papillary Carcinoma, Infiltrative Subtype"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Invasive Follicular Variant Thyroid Gland Papillary Carcinoma", "shortest_name_length": 61}
{"curie": "MONDO:0008187", "names": ["PAND1", "panic disorder", "panic disorder 1", "PANIC DISORDER 1", "panic disorder syndrome 1", "panic disorder with Joint laxity", "panic disorder, susceptibility to", "panic disorder with bladder conditions", "PANIC DISORDER SUSCEPTIBILITY LOCUS, CHROMOSOME 13q-RELATED", "panic disorder susceptibility locus, chromosome 13Q-related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "panic disorder 1", "shortest_name_length": 5}
{"curie": "MONDO:0017994", "names": ["severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency", "shortest_name_length": 78}
{"curie": "MONDO:0011520", "names": ["SLEB2", "susceptibility to systemic lupus erythematosus 2", "SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 2", "systemic lupus erythematosus, susceptibility to, 2", "systemic lupus erythematosus, susceptibility to, type 2", "SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 2 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "systemic lupus erythematosus, susceptibility to, 2", "shortest_name_length": 5}
{"curie": "MONDO:0001296", "names": ["Acquired night blindness", "acquired night blindness", "Night blindness, acquired", "Acquired night blindness (disorder)", "acquired night blindness (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired night blindness", "shortest_name_length": 24}
{"curie": "UMLS:C0282525", "names": ["NALD", "Intermediate PBD-ZSD", "Neonatal adrenoleucodystrophy", "Neonatal adrenoleukodystrophy", "Neonatal Adrenoleukodystrophy", "adrenoleukodystrophy neonatal", "neonatal adrenoleukodystrophy", "Adrenoleukodystrophy, Neonatal", "Neonatal Adrenoleukodystrophies", "Adrenoleukodystrophies, Neonatal", "Neonatal adrenoleukodystrophy (disorder)", "neonatal adrenoleukodystrophy (diagnosis)", "Adrenoleukodystrophy, Autosomal Neonatal Form", "Adrenoleukodystrophy, Autosomal, Neonatal Form", "Intermediate peroxisome biogenesis disorder-Zellweger spectrum disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adrenoleukodystrophy, Neonatal", "shortest_name_length": 4}
{"curie": "MONDO:0005065", "names": ["MESOTHELIOMA", "mesothelioma", "Mesothelioma", "mesotheliomas", "Mesotheliomas", "Mesothelioma, NOS", "Mesothelioma, unspecified", "mesothelioma; unspecified site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mesothelioma", "shortest_name_length": 12}
{"curie": "UMLS:C3899160", "names": ["Facial Nerve Palsy Related to Birth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Facial Nerve Palsy Related to Birth", "shortest_name_length": 35}
{"curie": "MONDO:0003530", "names": ["aggressive digital papillary adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aggressive digital papillary adenocarcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0002869", "names": ["Valvulopathy", "Valvular Disease", "Heart valve disease", "heart valve disease", "disease heart valve", "Heart Valve Disease", "valve heart disease", "Valvular abnormality", "heart valve disorder", "Heart Valve Diseases", "cardiac valvulopathy", "Heart Valve Prolapse", "heart valve prolapse", "Valve Disease, Heart", "heart valve diseases", "disease heart valves", "diseases heart valve", "Cardiac valvulopathy", "prolapse heart valve", "Heart valve disorder", "VALVULAR ABNORMALITY", "Heart Valve Disorder", "Cardiac valve disease", "Heart Valve Prolapses", "disorders heart valve", "heart valve disorders", "Heart valve disorders", "Prolapse, Heart Valve", "Valve Prolapse, Heart", "cardial valve disease", "HEART VALVE DISORDERS", "Valve Prolapses, Heart", "disease heart valvular", "VALVULAR HEART DISEASE", "cardiac valve disorder", "Valvular Heart Disease", "Cardiac valve prolapse", "Valvular abnormalities", "Heart valves--Diseases", "Prolapses, Heart Valve", "valvular heart disease", "Heart Valvular Disease", "heart valvular disease", "Valvular heart disease", "Disorder of heart valve", "Heart Disease, Valvular", "Valvular Disease, Heart", "Disease, Heart Valvular", "Heart Valvular Diseases", "Valvular Heart Diseases", "valvular heart disorder", "valvular heart diseases", "Cardiac valve disorders", "Valvular Heart Disorder", "Disorder of Heart Valve", "disorder of heart valve", "CARDIAC VALVULAR DISEASE", "cardiac valvular disease", "disease of cardial valve", "Heart valve disease, NOS", "disorder of cardial valve", "Heart valve disorder, NOS", "Valvular heart disease NOS", "Valvular heart disease, NOS", "disease (or disorder); valve", "Abnormality of the heart valves", "Heart valve disorder (disorder)", "Abnormal heart valve morphology", "cardial valve disease or disorder", "Cardiac valve prolapse (disorder)", "Cardiac valve prolapse (diagnosis)", "Valvular heart disease or syndrome", "valvular heart disease (diagnosis)", "disease or disorder of cardial valve", "Valvular Heart Diseases and Syndromes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heart valve disorder", "shortest_name_length": 12}
{"curie": "UMLS:C3163899", "names": ["Squamous cell carcinoma of nose", "Squamous cell carcinoma of nose (disorder)", "Squamous cell carcinoma of nose (diagnosis)", "malignant neoplasm carcinoma nose squamous cell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Squamous cell carcinoma of nose", "shortest_name_length": 31}
{"curie": "MONDO:0003586", "names": ["Esophagus Liposarcoma", "esophagus liposarcoma", "oesophagus liposarcoma", "Esophageal Liposarcoma", "esophageal liposarcoma", "liposarcoma of esophagus", "Liposarcoma of esophagus", "Liposarcoma of Esophagus", "Liposarcoma of oesophagus", "Liposarcoma of the Esophagus", "liposarcoma of the esophagus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophagus liposarcoma", "shortest_name_length": 21}
{"curie": "UMLS:C5419204", "names": ["Refractory Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Squamous Cell Carcinoma", "shortest_name_length": 34}
{"curie": "UMLS:C0578541", "names": ["Edema Trunk", "Edema trunk", "Oedema trunk", "Truncal edema", "Edema of trunk", "Oedema of trunk", "Edema of trunk (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Edema Trunk", "shortest_name_length": 11}
{"curie": "MONDO:0010482", "names": ["XPDS", "X-linked Parkinsonism with spasticity", "PARKINSONISM with spasticity, X-linked", "PARKINSONISM WITH SPASTICITY, X-LINKED", "X-linked parkinsonism-spasticity syndrome", "X-linked parkinsonism with spasticity syndrome", "XPDS - X-linked parkinsonism with spasticity syndrome", "X-linked parkinsonism with spasticity syndrome (disorder)", "Parkinsonism with spasticity, X-linked, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked parkinsonism-spasticity syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C4524857", "names": ["Refractory Malignant Solid Tumor", "Refractory Malignant Solid Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Malignant Solid Neoplasm", "shortest_name_length": 32}
{"curie": "UMLS:C1708788", "names": ["Lung NET G1", "Lung NET Grade 1", "Lung NET, Grade 1", "Lung Neuroendocrine Tumor G1", "Lung Typical Carcinoid Tumor", "Lung Neuroendocrine Tumor Grade 1", "Lung Neuroendocrine Tumor, Grade 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Typical Carcinoid Tumor", "shortest_name_length": 11}
{"curie": "MONDO:0019444", "names": ["trichinosis", "trichinoses", "TRICHINOSIS", "Trichinoses", "Trichinosis", "trichiniasis", "Trichiniasis", "TRICHINIASIS", "Trichinelloses", "Trichinellosis", "trichinellosis", "TRICHINELLIASIS", "Trichinelliases", "trichinelliasis", "Trichinelliasis", "Human trichinellosis", "trichinosis (diagnosis)", "infection with Trichinella", "Trichinella infectious disease", "Trichinella spiralis infection", "Trichinella disease or disorder", "Infection by larvae of Trichinella", "infection due to Trichinella species", "Trichinella caused disease or disorder", "Infection caused by larvae of Trichinella", "Infection caused by larvae of Trichinella (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichinellosis", "shortest_name_length": 11}
{"curie": "MONDO:0014524", "names": ["MRT47", "mental retardation, autosomal recessive 47", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 47", "intellectual disability, autosomal recessive 47", "mental retardation, autosomal recessive type 47", "intellectual disability, autosomal recessive type 47", "autosomal recessive intellectual developmental disorder 47", "intellectual developmental disorder, autosomal recessive 47", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 47", "FMN2 autosomal recessive non-syndromic intellectual disability", "autosomal recessive non-syndromic intellectual disability caused by mutation in FMN2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 47", "shortest_name_length": 5}
{"curie": "MONDO:0000654", "names": ["neoplasm of soft tissue", "neoplasm of soft tissues", "tumor of the soft tissue", "mesenchymal tissue neoplasm", "soft tissue benign neoplasm", "benign mesenchymal cell neoplasm", "Benign Mesenchymal Cell Neoplasm", "connective tissue benign neoplasm", "benign connective and soft tissue tumor", "Benign Connective and Soft Tissue Tumor", "Benign Tumor of the Soft Tissue and Bone", "benign tumor of the soft tissue and bone", "benign connective and soft tissue neoplasm", "Benign Connective and Soft Tissue Neoplasm", "CONNECTIVE AND SOFT TISSUE NEOPLASM, BENIGN", "benign neoplasm of the soft tissue and bone", "connective and soft tissue neoplasm, benign", "Benign Neoplasm of the Soft Tissue and Bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign connective and soft tissue neoplasm", "shortest_name_length": 23}
{"curie": "MONDO:0004528", "names": ["Palisaded Lymph Node Myofibroblastoma", "lymph node palisaded myofibroblastoma", "palisaded lymph node myofibroblastoma", "Palisaded Myofibroblastoma of Lymph Node", "palisaded myofibroblastoma of lymph node", "palisaded myofibroblastoma of the lymph node", "Palisaded Myofibroblastoma of the Lymph Node"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymph node palisaded myofibroblastoma", "shortest_name_length": 37}
{"curie": "MONDO:0024360", "names": ["central sleep apnea due to high altitude", "Central sleep apnea due to high altitude", "Central sleep apnoea due to high altitude", "central sleep apnea caused by high altitude", "Central sleep apnea caused by high altitude", "Central sleep apnoea caused by high altitude", "Central sleep apnea caused by high altitude (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central sleep apnea caused by high altitude", "shortest_name_length": 40}
{"curie": "UMLS:C5446647", "names": ["Metastatic Endometrial Clear Cell Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Endometrial Clear Cell Adenocarcinoma", "shortest_name_length": 48}
{"curie": "MONDO:0017597", "names": ["THRLBCL", "T-cell/histiocyte rich lymphoma", "T-Cell/Histiocyte Rich Lymphoma", "T-cell rich large B-cell lymphoma", "Histiocyte-rich large B-cell lymphoma", "T-Cell/Histiocyte-Rich Large B-Cell Lymphoma", "T-cell histiocyte rich large B-cell lymphoma", "T-cell/histiocyte rich large B cell lymphoma", "T-cell/histiocyte rich large B-cell lymphoma", "T-cell/histiocyte-rich large B-cell lymphoma", "T-cell hystiocyte rich large B-cell lymphoma", "T-Cell Rich/Histiocyte-Rich Large B-Cell Lymphoma", "T-cell rich/histiocyte-rich large B-cell lymphoma", "T-cell histiocyte rich large B-cell lymphoma (disorder)", "T-cell/histiocyte rich large B-cell lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-cell/histiocyte rich large B cell lymphoma", "shortest_name_length": 7}
{"curie": "MONDO:0002804", "names": ["Apocrine adenoma", "apocrine adenoma", "adenoma apocrine", "Apocrine Adenoma", "[M]Apocrine adenoma", "apocrine cystadenoma", "apocrine hidrocystoma", "Tubular Apocrine Adenoma", "tubular apocrine adenoma", "tubular Apocrine adenoma", "Tubular apocrine adenoma", "Apocrine adenoma (disorder)", "Apocrine adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "apocrine adenoma", "shortest_name_length": 16}
{"curie": "UMLS:C4521729", "names": ["Stage IVB Esophageal Squamous Cell Cancer", "Clinical Stage IVB Esophageal Squamous Cell Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage IVB Esophageal Squamous Cell Carcinoma AJCC v8", "shortest_name_length": 41}
{"curie": "UMLS:C5667138", "names": ["Recurrent Glioblastoma, IDH-Mutant", "Recurrent Astrocytoma, IDH-Mutant, Grade 4", "Recurrent Astrocytoma, IDH-Mutant, Grade IV"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Astrocytoma, IDH-Mutant, Grade 4", "shortest_name_length": 34}
{"curie": "MONDO:0009892", "names": ["ECYT2", "Chuvash polycythemia", "Chuvash erythromatosis", "Chuvash erythrocytosis", "Chuvash type polycythemia", "VHL familial polycythemia", "familial erythrocytosis 2", "POLYCYTHEMIA, CHUVASH TYPE", "Polycythemia, Chuvash Type", "polycythemia, Chuvash type", "erythrocytosis, familial, 2", "ERYTHROCYTOSIS, FAMILIAL, 2", "Erythrocytosis, Familial, 2", "polycythemia, VHL-dependent", "Polycythemia, VHL-Dependent", "POLYCYTHEMIA, VHL-DEPENDENT", "erythrocytosis, familial, type 2", "Von Hippel-Lindau-dependent polycythemia", "autosomal recessive benign erythrocytosis", "Erythrocytosis, Autosomal Recessive Benign", "erythrocytosis, autosomal recessive benign", "familial polycythemia caused by mutation in VHL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chuvash polycythemia", "shortest_name_length": 5}
{"curie": "UMLS:C0278590", "names": ["Recurrent Ewing Sarcoma", "Relapsed Ewing's Sarcoma", "Recurrent Ewing's Sarcoma", "Ewing's sarcoma recurrent", "recurrent Ewing's sarcoma", "Ewing's Sarcoma, Recurrent", "Ewing's sarcoma, recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ewing's sarcoma recurrent", "shortest_name_length": 23}
{"curie": "MONDO:0009214", "names": ["FA4", "Fad2", "FAD2", "FACD", "FANCD", "FANCD2", "Fanconi pancytopenia type 4", "Fanconi pancytopenia, type 4", "FANCONI PANCYTOPENIA, TYPE 4", "Fanconi Anemia, complementation group D", "FANCONI ANEMIA, COMPLEMENTATION GROUP D", "Fanconi anemia complementation group D2", "Fanconi anemia, complementation group D2", "FANCONI ANEMIA, COMPLEMENTATION GROUP D2", "Fanconi Anemia, Complementation Group D2", "Fanconi anemia complementation group D2 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fanconi anemia complementation group D2", "shortest_name_length": 3}
{"curie": "UMLS:C1710535", "names": ["Undifferentiated Stromal Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Undifferentiated Stromal Sarcoma", "shortest_name_length": 32}
{"curie": "MONDO:0010485", "names": ["MCOPS13", "MAINE MICROPHTHALMOS", "Maine microphthalmos", "syndromic microphthalmia 13", "microphthalmia, syndromic 13", "MICROPHTHALMIA, SYNDROMIC 13", "microphthalmia, syndromic type 13", "colobomatous microphthalmia with microcephaly, short stature, and psychomotor retardation", "COLOBOMATOUS MICROPHTHALMIA WITH MICROCEPHALY, SHORT STATURE, AND PSYCHOMOTOR RETARDATION", "X-linked colobomatous microphthalmia-microcephaly-intellectual disability-short stature syndrome", "X-linked colobomatous microphthalmia-microcephaly-short stature-psychomotor retardation syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked colobomatous microphthalmia-microcephaly-intellectual disability-short stature syndrome", "shortest_name_length": 7}
{"curie": "MONDO:0014308", "names": ["ETL6", "familial temporal lobe epilepsy 6", "epilepsy, familial temporal lobe, 6", "EPILEPSY, FAMILIAL TEMPORAL LOBE, 6", "familial temporal lobe epilepsy type 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial temporal lobe epilepsy 6", "shortest_name_length": 4}
{"curie": "MONDO:0020628", "names": ["MGRISCE2", "MICROCEPHALY, GROWTH RESTRICTION, AND INCREASED SISTER CHROMATID EXCHANGE 2", "microcephaly, growth restriction, and increased sister chromatid exchange 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly, growth restriction, and increased sister chromatid exchange 2", "shortest_name_length": 8}
{"curie": "MONDO:0030797", "names": ["RP93", "RETINITIS PIGMENTOSA 93", "retinitis pigmentosa 93"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 93", "shortest_name_length": 4}
{"curie": "MONDO:0008449", "names": ["NTD", "Open spine", "Open Spine", "Split spine", "Spine, Open", "Open Spines", "Cleft spine", "Cleft Spine", "Spina Bifida", "Spine, Cleft", "SPINA BIFIDA", "Cleft Spines", "Spina bifida", "spina bifida", "Rachischisis", "rachischisis", "Bifida, Spina", "Spina Bifidas", "Schistorrhachis", "spinal myelocele", "Spinal Dysraphia", "Spinal Myelocele", "Spinal Dysraphism", "Spina bifida, NOS", "Spinal dysrhaphia", "Dysraphia, Spinal", "spinal dysraphism", "Spinal Dysraphias", "Spinal dysraphism", "SB - Spina bifida", "Spinal Dysraphisms", "Dysraphism, Spinal", "spinal meningocele", "Spinal Meningocele", "Dysraphisms, Spinal", "spina bifida (disease)", "Posterior rachischisis", "Spinal Myelomeningocele", "spinal myelomeningocele", "SPINA BIFIDA CONGENITAL", "Spina bifida (disorder)", "spina bifida (diagnosis)", "Defective spinal closure", "Spina bifida, unspecified", "neural tube defects, susceptibility to", "Incomplete closure of the vertebral arch"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spina bifida", "shortest_name_length": 3}
{"curie": "UMLS:C0270202", "names": ["ABO isoimmunization", "ABO isoimmunisation", "ABO Isoimmunization", "Anemia due to ABO antibodies", "ABO isoimmunization of newborn", "Jaundice due to ABO antibodies", "ABO Hemolytic Disease of Newborn", "ABO hemolytic disease of newborn", "Anemia due to ABO isoimmunization", "anemia due to ABO isoimmunization", "ABO haemolytic disease of newborn", "ABO isoimmunisation of the newborn", "ABO isoimmunization of the newborn", "Jaundice due to ABO isoimmunization", "ABO hemolytic disease of the newborn", "ABO Hemolytic Disease of the Newborn", "ABO haemolytic disease of the newborn", "Erythroblastosis due to ABO antibodies", "fetal; jaundice, due to ABO antibodies", "ABO isoimmunisation of fetus and newborn", "ABO isoimmunization of fetus and newborn", "Erythroblastosis due to ABO isoimmunization", "fetal; jaundice, due to ABO isoimmunization", "Hemolytic Disease due to ABO Isoimmunization", "Hemolytic disease due to ABO isoimmunization", "anemia due to ABO isoimmunization (diagnosis)", "Haemolytic disease due to ABO isoimmunization", "newborn; jaundice, due to ABO isoimmunization", "Haemolytic disease due to ABO isoimmunisation", "Erythroblastosis fetalis due to ABO antibodies", "ABO HDN - ABO hemolytic disease of the newborn", "ABO HDN - ABO haemolytic disease of the newborn", "Hemolytic disease of fetus due to ABO antibodies", "Anemia due to ABO maternal/fetal incompatibility", "Anemia due to ABO incompatibility in the newborn", "Anaemia due to ABO incompatibility in the newborn", "Hemolytic disease of newborn due to ABO antibodies", "Jaundice due to ABO isoimmunisation of the newborn", "Jaundice due to ABO isoimmunization of the newborn", "Jaundice due to ABO maternal/fetal incompatibility", "Erythroblastosis fetalis due to ABO isoimmunisation", "Erythroblastosis fetalis due to ABO isoimmunization", "erythroblastosis fetalis due to ABO isoimmunization", "Erythroblastosis foetalis due to ABO isoimmunization", "Erythroblastosis foetalis due to ABO isoimmunisation", "Hemolytic disease of fetus due to ABO isoimmunization", "fetal or neonatal hemolysis due to ABO isoimmunization", "Hemolytic disease of newborn due to ABO incompatibility", "Hemolytic disease of newborn due to ABO isoimmunization", "Erythroblastosis due to ABO maternal/fetal incompatibility", "fetal; jaundice, due to ABO incompatibility, maternal/fetal", "Hemolytic disease of fetus OR newborn due to ABO immunization", "Hemolytic disease of fetus or newborn due to ABO immunization", "Haemolytic disease of fetus OR newborn due to ABO immunisation", "Haemolytic disease of foetus or newborn due to ABO immunization", "erythroblastosis fetalis due to ABO isoimmunization (diagnosis)", "Haemolytic disease of foetus OR newborn due to ABO immunisation", "Hemolytic disease of fetus or newborn due to ABO isoimmunization", "Erythroblastosis fetalis due to ABO maternal/fetal incompatibility", "fetal or neonatal hemolysis due to ABO isoimmunization (diagnosis)", "Hemolytic disease of fetus due to ABO maternal/fetal incompatibility", "Hemolytic disease of newborn due to ABO maternal/fetal incompatibility", "Hemolytic disease of fetus OR newborn due to ABO immunization (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemolytic disease of fetus OR newborn due to ABO immunization", "shortest_name_length": 19}
{"curie": "MONDO:0014513", "names": ["NEM10", "NEMALINE MYOPATHY 10", "nemaline myopathy 10", "congenital myopathy 10", "LMOD3 nemaline myopathy", "nemaline myopathy type 10", "nemaline myopathy caused by mutation in LMOD3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nemaline myopathy 10", "shortest_name_length": 5}
{"curie": "UMLS:C1299641", "names": ["Extravasation injury", "Extravasation injury (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extravasation injury", "shortest_name_length": 20}
{"curie": "UMLS:C0752219", "names": ["diffuse axonal injury", "axonal diffuse injury", "Diffuse axonal injury", "Diffuse Axonal Injury", "Axonal Injury, Diffuse", "Injury, Diffuse Axonal", "diffuse axonal injuries", "Diffuse Axonal Injuries", "Injuries, Diffuse Axonal", "Axonal Injuries, Diffuse", "DAI (Diffuse Axonal Injury)", "DAIs (Diffuse Axonal Injury)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse Axonal Injury", "shortest_name_length": 21}
{"curie": "MONDO:0019525", "names": ["tetra X", "48 XXXX", "Tetra X", "Tetrasomy X", "tetrasomy X", "Quadruple X", "quadruple X", "tetrasomy x", "XXXX syndrome", "xxxx syndrome", "syndrome; XXXX", "XXXX; syndrome", "Four X syndrome", "48,XXXX syndrome", "48 XXXX syndrome", "tetrasomy type X", "XXXX syndrome; female", "XXXX syndrome, female", "Tetra X syndrome, female", "Four X syndrome (disorder)", "syndrome; XXXX, female, 48,XXXX"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tetrasomy X", "shortest_name_length": 7}
{"curie": "MONDO:0012781", "names": ["CELIAC12", "CELIAC DISEASE, SUSCEPTIBILITY TO, 12", "celiac disease, susceptibility to, 12", "GLUTEN-SENSITIVE ENTEROPATHY, SUSCEPTIBILITY TO, 12", "gluten-sensitive enteropathy, susceptibility to, 12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "celiac disease, susceptibility to, 12", "shortest_name_length": 8}
{"curie": "MONDO:0007894", "names": ["Leri pleonosteosis", "LERI PLEONOSTEOSIS", "Leri's pleonosteosis", "pleonosteosis Leri type", "Leri type pleonosteosis", "CHROMOSOME 8q22.1 DUPLICATION SYNDROME", "chromosome 8q22.1 DUPLICATION syndrome", "leri pleonosteosis chromosome duplication syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leri pleonosteosis", "shortest_name_length": 18}
{"curie": "MONDO:0019680", "names": ["genochondromatosis type 2", "Genochondromatosis type 2", "Genochondromatosis type 2 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genochondromatosis type 2", "shortest_name_length": 25}
{"curie": "UMLS:C5554634", "names": ["Metastatic Lung Large Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Lung Large Cell Neuroendocrine Carcinoma", "shortest_name_length": 51}
{"curie": "MONDO:0007372", "names": ["CNA1", "CORNEA PLANA 1", "Cornea Plana 1", "cornea plana 1", "cornea plana 1, autosomal dominant", "CORNEA PLANA 1, AUTOSOMAL DOMINANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cornea plana 1, autosomal dominant", "shortest_name_length": 4}
{"curie": "MONDO:0019967", "names": ["Lunatomalacia", "Kienbock disease", "Kienbock's disease", "bilateral Kienbock's disease", "osteochondritis of the lunate bone", "Osteochondrosis of the lunate bone", "aseptic necrosis of the lunate bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kienbock disease", "shortest_name_length": 13}
{"curie": "MONDO:0011227", "names": ["SAM", "SAMS", "Sams", "SAMS syndrome", "Systolic anterior movement of mitral valve", "mitral valve prolapse systolic anterior movement", "Systolic anterior movement of mitral valve (disorder)", "Systolic anterior movement of mitral valve (diagnosis)", "Short Stature, Auditory Canal Atresia, Mandibular Hypoplasia, Skeletal Abnormalities", "SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, SKELETAL ABNORMALITIES", "short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities", "short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome", "SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, AND SKELETAL ABNORMALITIES", "short stature, auditory canal atresia, mandibular hypoplasia, and skeletal abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C2699052", "names": ["Reproductive System Stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reproductive System Stenosis", "shortest_name_length": 28}
{"curie": "MONDO:0015306", "names": ["necrobacillosis", "Necrobacillosis", "Necrobacilloses", "NECROBACILLOSIS", "Lemierre Disease", "acute sore throat", "Lemierre syndrome", "Disease, Lemierre", "Lemierres Disease", "Lemierre Syndrome", "Syndrome, Lemierre", "Lemierres Syndrome", "Lemierre's Disease", "Postanginal Sepsis", "Postanginal Sepses", "postanginal sepsis", "Lemierre's Syndrome", "Sepsis, Postanginal", "Disease, Lemierre's", "Sepses, Postanginal", "Lemierre's syndrome", "Syndrome, Lemierre's", "Necrobacillosis, NOS", "human necrobacillosis", "Fusobacterium Infection", "Fusobacterium infection", "Sphaerophorus Infection", "Infection, Sphaerophorus", "Fusobacterium Infections", "Infection, Fusobacterium", "Fusobacterium infections", "Sphaerophorus Infections", "Infections, Fusobacterium", "Infections, Sphaerophorus", "Necrobacillosis (disorder)", "Lemierre postanginal sepsis", "necrobacillosis (diagnosis)", "Lemierre syndrome (disorder)", "Septic phlebitis of internal jugular vein", "septic phlebitis of the internal jugular vein", "Septic phlebitis of the internal jugular vein", "postanginal sepsis secondary to orophyngeal infection", "Postanginal sepsis secondary to orophyngeal infection", "Postanginal sepsis secondary to oropharyngeal infection", "oropharyngeal infection leading to secondary septic thrombophlebitis of the internal jugular vein"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lemierre syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0004048", "names": ["Gastric Immature Teratoma", "immature gastric teratoma", "Immature Gastric Teratoma", "malignant gastric teratoma", "stomach malignant teratoma", "malignant teratoma of stomach", "malignant teratoma of the stomach"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immature gastric teratoma", "shortest_name_length": 25}
{"curie": "MONDO:0012760", "names": ["EIG5", "idiopathic generalized epilepsy 5", "epilepsy, idiopathic generalized, susceptibility to, 5", "EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 5", "epilepsy, idiopathic generalized, susceptibility to, locus on chromosome 10", "EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, LOCUS ON CHROMOSOME 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, idiopathic generalized, susceptibility to, 5", "shortest_name_length": 4}
{"curie": "MONDO:0009737", "names": ["GSL", "NGBE", "PPCA deficiency", "PPCA DEFICIENCY", "galactosialidosis", "Galactosialidosis", "Goldberg syndrome", "goldberg syndrome", "GALACTOSIALIDOSIS", "GOLDBERG SYNDROME", "Goldberg Syndrome", "CATHEPSIN A DEFICIENCY", "Cathepsin A Deficiency", "cathepsin A deficiency", "GSL - Galactosialidosis", "cathepsin A deficiency of", "Deficiency of Cathepsin A", "Cathepsin A, deficiency of", "Protective protein deficiency", "Lysosomal Protective Protein Deficiency", "lysosomal protective Protein deficiency", "LYSOSOMAL PROTECTIVE PROTEIN DEFICIENCY", "PROTECTIVE PROTEIN/CATHEPSIN A DEFICIENCY", "protective Protein/Cathepsin a deficiency", "Protective protein-Cathepsin A deficiency", "lysosomal protective protein deficiency of", "NEURAMINIDASE/BETA-GALACTOSIDASE EXPRESSION", "Lysosomal protective protein, deficiency of", "neuraminidase/Beta-galactosidase expression", "Combined deficiency of sialidase AND beta galactosidase", "Combined deficiency of sialidase and beta galactosidase", "Neuraminidase deficiency with beta-galactosidase deficiency", "Neuraminidase Deficiency with Beta-Galactosidase Deficiency", "NEURAMINIDASE DEFICIENCY WITH BETA-GALACTOSIDASE DEFICIENCY", "neuraminidase deficiency with beta-galactosidase deficiency", "Combined deficiency of neuroaminidase and beta galactosidase", "Combined deficiency of sialidase AND beta galactosidase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "galactosialidosis", "shortest_name_length": 3}
{"curie": "MONDO:0014900", "names": ["LGMD2Y", "MRRSDC", "LGMD type 2Y", "TOR1AIP1-related LGMD", "TOR1AIP1-Related LGMD", "muscular dystrophy, limb-girdle, type 2y", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Y", "muscular dystrophy, limb-girdle, type 2Y", "TOR1AIP1-related limb-girdle muscular dystrophy", "TOR1AIP1-Related Limb-Girdle Muscular Dystrophy", "Autosomal recessive limb girdle muscular dystrophy type 2Y", "Autosomal recessive limb-girdle muscular dystrophy type 2Y", "autosomal recessive limb-girdle muscular dystrophy type 2Y", "Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2Y", "TOR1AIP1 autosomal recessive limb-girdle muscular dystrophy", "Autosomal recessive muscular dystrophy due to LAP1B deficiency", "autosomal recessive muscular dystrophy due to LAP1B deficiency", "Autosomal recessive limb girdle muscular dystrophy type 2Y (disorder)", "MYOPATHY, AUTOSOMAL RECESSIVE, WITH RIGID SPINE AND DISTAL JOINT CONTRACTURES", "Muscular dystrophy with progressive weakness, distal contracture and rigid spine", "muscular dystrophy with progressive weakness, distal contractures and rigid spine", "Muscular dystrophy with progressive weakness, distal contractures and rigid spine", "autosomal recessive limb-girdle muscular dystrophy caused by mutation in TOR1AIP1", "Muscular Dystrophy, Autosomal Recessive, with Rigid Spine and Distal Joint Contractures", "muscular dystrophy, autosomal recessive, with rigid spine and distal joint contractures", "autosomal recessive muscular dystrophy due to Torsin-1A-interacting protein 1 deficiency", "Autosomal recessive muscular dystrophy due to Torsin-1A-interacting protein 1 deficiency", "Autosomal recessive muscular dystrophy due to LAP1B (lamin-associated protein 1B) deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive limb-girdle muscular dystrophy type 2Y", "shortest_name_length": 6}
{"curie": "MONDO:0009076", "names": ["DFNB1", "DFNB1A", "connexin 26 deafness", "GJB2-related deafness", "DEAFNESS, DIGENIC, GJB2/GJB6", "DEAFNESS, DIGENIC, GJB2/GJB3", "Deafness, Digenic, Gjb2-Gjb3", "deafness, digenic, GJB2/GJB6", "deafness, digenic, GJB2/GJB3", "Deafness, Digenic, Gjb2-Gjb6", "autosomal recessive deafness 1A", "deafness, autosomal recessive 1A", "DEAFNESS, AUTOSOMAL RECESSIVE 1A", "Deafness, Autosomal Recessive 1A", "deafness, autosomal recessive type 1A", "DEAFNESS, DIGENIC, GJB2/GJB3 (disorder)", "DEAFNESS, DIGENIC, GJB2/GJB6 (disorder)", "deafness nonsyndromic, connexin 26 linked", "DEAFNESS, AUTOSOMAL RECESSIVE 1A (disorder)", "autosomal recessive nonsyndromic deafness 1A", "autosomal recessive nonsyndromic hearing loss 1A", "autosomal recessive nonsyndromic deafness type 1A", "deafness, digenic GJB2/GJB6, Autosomal recessive, Digenic dominant", "deafness, digenic, GJB2/GJB3, Autosomal recessive, Digenic dominant", "deafness, autosomal recessive 1a, autosomal recessive, digenic dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 1A", "shortest_name_length": 5}
{"curie": "MONDO:0001809", "names": ["uterus; band", "band; uterus", "band of uterus", "Band of uterus", "Bands of uterus", "uterus adhesions", "uterus; adhesion", "adhesion; uterus", "UTERINE ADHESION", "Uterine synechiae", "Uterine adhesions", "uterine adhesions", "adhesions of uterus", "Adhesions of uterus", "intrauterine adhesion", "synechia; intrauterine", "intrauterine; synechia", "Intrauterine Synechiae", "intrauterine adhesions", "Intrauterine synechiae", "intrauterine synechiae", "Intrauterine adhesions", "adhesions intrauterine", "SYNECHIAE, INTRAUTERINE", "uterine adhesions (diagnosis)", "Adhesions of uterus (disorder)", "Intrauterine adhesions (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adhesions of uterus", "shortest_name_length": 12}
{"curie": "MONDO:0011874", "names": ["IHSC", "Ilvasc", "ILVASC", "Nisch Syndrome", "Nisch syndrome", "NISCH SYNDROME", "NISCH syndrome", "ichthyosis-sclerosing cholangitis syndrome", "ICHTHYOSIS-SCLEROSING CHOLANGITIS SYNDROME", "Ichthyosis-Sclerosing Cholangitis Syndrome", "Neonatal ichthyosis-sclerosing cholangitis syndrome", "Neonatal Ichthyosis-Sclerosing Cholangitis Syndrome", "NEONATAL ICHTHYOSIS-SCLEROSING CHOLANGITIS SYNDROME", "neonatal ichthyosis-sclerosing cholangitis syndrome", "ichthyosis-hypotrichosis-sclerosing cholangitis syndrome", "Ichthyosis-hypotrichosis-sclerosing cholangitis syndrome", "Ichthyosis, hypotrichosis, sclerosing cholangitis syndrome", "Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome", "Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis", "ICHTHYOSIS, LEUKOCYTE VACUOLES, ALOPECIA, AND SCLEROSING CHOLANGITIS", "ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis", "NISCH (neonatal ichthyosis, sclerosing cholangitis, hypotrichosis) syndrome", "Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal ichthyosis-sclerosing cholangitis syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0010383", "names": ["FXS", "FraX syndrome", "FRAXA syndrome", "fra(X) syndrome", "Fra(X) Syndrome", "mar(X) syndrome", "Marker X Syndrome", "MARKER X SYNDROME", "marker X syndrome", "Marker X syndrome", "fragile syndrome x", "Syndrome, Marker X", "Marker X Syndromes", "fragile x syndrome", "marker 10 syndrome", "fragile X syndrome", "Fragile X Syndrome", "fragile-x syndrome", "fragile-X syndrome", "FRAGILE X SYNDROME", "x fragile syndrome", "Fragile X syndrome", "Escalante syndrome", "Syndromes, Marker X", "fra(X)(28) syndrome", "fragile 10 syndrome", "fragile Xq syndrome", "fragile X; syndrome", "Fragile X Syndromes", "Syndrome, Fragile X", "syndrome; fragile X", "Martin-Bell Syndrome", "MARTIN-BELL SYNDROME", "fra(X)(q27) syndrome", "Martin-Bell syndrome", "Martin Bell Syndrome", "Syndromes, Fragile X", "martin bell syndrome", "martin-bell syndrome", "Syndrome, Martin-Bell", "Renpenning syndrome 2", "fra(X)(q27-28) syndrome", "fragile-X syndrome (FXS)", "fragile x syndrome autism", "autism fragile syndrome x", "autism-fragile X syndrome", "FRAXA - Fragile X syndrome", "Martin-Bell syndrome (MBS)", "disorder fragile x syndrome", "Fragile X syndrome (disorder)", "fragile X syndrome (diagnosis)", "Martin-Bell-Renpenning syndrome", "chromosome X fragility syndrome", "macro-orchidism-marker X syndrome", "fragile site mental retardation 1", "autism-fragile X (AFRAX) syndrome", "fragile 10 premature ovarian failure", "fragile X-mental retardation syndrome", "FRAGILE X MENTAL RETARDATION SYNDROME", "Fragile X syndrome, X-linked dominant", "Fragile X Mental Retardation Syndrome", "fragile X mental retardation syndrome", "fragile 10 mental retardation syndrome", "fragile site mental retardation 1 (FMR1)", "macro-orchidism-marker X (MOMX) syndrome", "mental retardation-macroorchidism syndrome", "fragile X intellectual disability syndrome", "fragile 10 intellectual disability syndrome", "X-Linked Mental Retardation and Macroorchidism", "X-LINKED MENTAL RETARDATION AND MACROORCHIDISM", "X-linked mental retardation and macroorchidism", "X Linked Mental Retardation and Macroorchidism", "X-linked mental deficiency-megalotestes syndrome", "X-linked mental retardation-fragile site 1 syndrome", "X-linked intellectual disability and macroorchidism", "X-linked mental retardation with fragile X syndrome", "primary ovarian insufficiency, fragile X-associated", "mental retardation, X-linked, associated with Marxq28", "Mental Retardation, X-Linked, Associated With Marxq28", "MENTAL RETARDATION, X-LINKED, ASSOCIATED WITH marXq28", "intellectual disability, X-linked, associated with Marxq28", "X-linked mental retardation-fragile site 1 syndrome (FRAXE 1)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fragile X syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0019019", "names": ["OI", "Brittle bones", "Vrolik disease", "Vrolik's disease", "Osteopsathyrosis", "Lobstein disease", "osteopsathyrosis", "OSTEOPSATHYROSIS", "fragility; ossium", "Fragilitas Ossium", "Fragilitas ossium", "ossium; fragility", "glass bone disease", "Glass bone disease", "Lobstein's syndrome", "Ossiums, Fragilitas", "brittle bone disease", "Brittle bone disease", "Brittle Bone Disease", "Brittle bone syndrome", "fragilitans; osteitis", "osteitis; fragilitans", "brittle bone syndrome", "Osteogenesis imperfecta", "osteogenesis imperfecta", "Osteogenesis Imperfecta", "OSTEOGENESIS IMPERFECTA", "Porak and Durante disease", "OI - Osteogenesis imperfecta", "Osteogenesis imperfecta, NOS", "Osteogenesis imperfecta (disorder)", "osteogenesis imperfecta (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteogenesis imperfecta", "shortest_name_length": 2}
{"curie": "MONDO:0013915", "names": ["HH13", "KISS1 hypogonadotropic hypogonadism", "hypogonadotropic hypogonadism 13 with or without anosmia", "HYPOGONADOTROPIC HYPOGONADISM 13 WITH OR WITHOUT ANOSMIA", "hypogonadotropic hypogonadism caused by mutation in KISS1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadotropic hypogonadism 13 with or without anosmia", "shortest_name_length": 4}
{"curie": "UMLS:C1334029", "names": ["Hindgut Carcinoid Tumor", "Hindgut Neuroendocrine Tumor G1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hindgut Neuroendocrine Tumor G1", "shortest_name_length": 23}
{"curie": "UMLS:C0417713", "names": ["cat bite", "Cat Bite", "Cat bite", "bite cat", "Cat Bites", "bites cat", "Cat bites", "bites cats", "Bite of cats", "Bitten by cat", "Cat bite (event)", "cat bite (diagnosis)", "injury caused by cat bite"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cat bite", "shortest_name_length": 8}
{"curie": "MONDO:0016979", "names": ["MRCS syndrome", "microcornea-rod-cone dystrophy-cataract-posterior staphyloma syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MRCS syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0012235", "names": ["SCAR7", "Spinocerebellar Ataxia Autosomal Recessive 7", "spinocerebellar ataxia autosomal recessive 7", "autosomal recessive spinocerebellar ataxia 7", "Spinocerebellar Ataxia, Autosomal Recessive 7", "spinocerebellar ataxia, autosomal recessive 7", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7", "autosomal recessive spinocerebellar ataxia type 7", "Autosomal recessive spinocerebellar ataxia type 7", "spinocerebellar ataxia, autosomal recessive type 7", "SCAR7 Spinocerebellar Ataxia Autosomal Recessive 7", "SCAR7 - autosomal recessive spinocerebellar ataxia type 7", "Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia", "childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia", "childhood onset autosomal recessive slowly progressive spinocerebellar ataxia", "Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive spinocerebellar ataxia 7", "shortest_name_length": 5}
{"curie": "UMLS:C4521608", "names": ["Stage IB Pleural Malignant Mesothelioma", "Stage IB Pleural Malignant Mesothelioma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Pleural Malignant Mesothelioma AJCC v8", "shortest_name_length": 39}
{"curie": "MONDO:0020642", "names": ["Sponge kidney", "Polycystic Kidney", "polycystic kidney", "KIDNEY POLYCYSTIC", "Polycystic kidney", "POLYCYSTIC KIDNEY", "Kidney polycystic", "polycystic; kidney", "Kidney, Polycystic", "polycystic kidneys", "KIDNEY, POLYCYSTIC", "Polycystic kidneys", "kidney; polycystic", "Polycystic Kidneys", "Kidneys, Polycystic", "Cystic kidney disease", "cyst; kidney, multiple", "kidney; cyst, multiple", "congenital cysts kidney", "polycystic renal disease", "Polycystic Renal Disease", "POLYCYSTIC RENAL DISEASE", "Congenital cyst of kidney", "polycystic kidney disease", "Polycystic Kidney Disease", "Polycystic kidney disease", "Polycystic Renal Diseases", "Renal Disease, Polycystic", "POLYCYSTIC KIDNEY DISEASE", "Fibrocystic Renal Disease", "fibrocystic renal disease", "Disease, Polycystic Renal", "Polycystic Kidney Diseases", "Diseases, Polycystic Renal", "Renal Diseases, Polycystic", "polycystic kidney diseases", "KIDNEY, POLYCYSTIC DISEASE", "Disease, Polycystic Kidney", "Kidney Disease, Polycystic", "Diseases, Polycystic Kidney", "Kidney Diseases, Polycystic", "Polycystic kidney dysplasia", "Enlarged polycystic kidneys", "congenital polycystic kidney", "polycystic kidney (diagnosis)", "Polycystic Kidney - body part", "Polycystic kidney, unspecified", "PCK - Polycystic kidney disease", "PKD - Polycystic kidney disease", "PKD - Polycystic Kidney Disease", "PKD - polycystic kidney disease", "Congenital cystic kidney disease", "cystic; renal disease, congenital", "Cystic kidney disease, unspecified", "renal; disease, cystic, congenital", "Multiple congenital cysts of kidney", "Polycystic kidney, unspecified type", "Congenital cystic disease of kidney", "Congenital polycystic kidney disease", "Polycystic kidney disease (disorder)", "Congenital cystic kidney disease (disorder)", "disease (or disorder); renal, cystic, congenital", "disease (or disorder); cystic, kidney, congenital", "disease (or disorder); kidney, cystic (congenital)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polycystic kidney disease", "shortest_name_length": 13}
{"curie": "MONDO:0020587", "names": ["factor XI deficiency", "Factor XI deficiency", "Factor XI Deficiency", "Factor XI deficiency (disorder)", "factor XI deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "factor XI deficiency", "shortest_name_length": 20}
{"curie": "MONDO:0006026", "names": ["bladder disease", "disease bladder", "Bladder Disease", "bladder diseases", "Bladder Diseases", "Bladder disorder", "bladder disorder", "Bladder Disorder", "BLADDER DISORDER", "bladder disorders", "Bladder Disorders", "Bladder--Diseases", "Disorder of bladder", "disorder of bladder", "Bladder disorder NOS", "Urinary Bladder Disease", "Disease of bladder, NOS", "diseases of the bladder", "urinary bladder disease", "DISEASES OF THE BLADDER", "Disorder of bladder, NOS", "Urinary Bladder Disorder", "urinary bladder disorder", "Urinary Bladder Diseases", "disease of urinary bladder", "Disorder of urinary bladder", "Bladder disease or syndrome", "disorder of urinary bladder", "Bladder disorder, unspecified", "disease (or disorder); bladder", "disorder of bladder (diagnosis)", "Unspecified disorder of bladder", "urinary bladder disease or disorder", "Disorder of bladder and bladder neck", "Disorder of urinary bladder (disorder)", "disease (or disorder); urinary bladder", "disease or disorder of urinary bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urinary bladder disorder", "shortest_name_length": 15}
{"curie": "MONDO:0030378", "names": ["COXPD53", "ELBRACHT-ISIKAY SYNDROME", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 53", "combined oxidative phosphorylation deficiency 53", "combined oxidative phosphorylation deficiency due to C2orf69 deficiency", "GLOBAL DEVELOPMENTAL DELAY, PROGRESSIVE MICROCEPHALY, STRUCTURAL BRAIN ABNORMALITIES, AND AUTOINFLAMMATION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation deficiency 53", "shortest_name_length": 7}
{"curie": "MONDO:0001767", "names": ["Punctal stenosis", "punctal stenosis", "Lacrimal punctum stenosis", "stenosis of lacrimal punctum", "Stenosis of lacrimal punctum", "Stenosis of the lacrimal punctum", "punctal stenosis (physical finding)", "Stenosis of lacrimal punctum (disorder)", "stenosis of lacrimal punctum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stenosis of lacrimal punctum", "shortest_name_length": 16}
{"curie": "UMLS:C4527056", "names": ["Merkel Cell Carcinoma by AJCC v8 Clinical Stage", "Neuroendocrine Carcinoma of the Skin by AJCC v8 Clinical Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Merkel Cell Carcinoma by AJCC v8 Clinical Stage", "shortest_name_length": 47}
{"curie": "MONDO:0015570", "names": ["isolated congenital auditory ossicle malformation", "congenital auditory ossicle malformation without external ear abnormality"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated congenital auditory ossicle malformation", "shortest_name_length": 49}
{"curie": "MONDO:0042956", "names": ["Saal-Bulas syndrome", "Saal Bulas syndrome", "ectrodactyly, diaphragmatic hernia, congenital heart defect, and agenesis of the corpus callosum", "Ectrodactyly, diaphragmatic hernia, congenital heart defect, and agenesis of the corpus callosum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Saal-Bulas syndrome", "shortest_name_length": 19}
{"curie": "UMLS:C1336133", "names": ["fallopian tube cancer stage IB", "stage IB fallopian tube cancer", "Fallopian Tube Cancer Stage IB", "Stage IB Fallopian Tube Cancer", "AJCC Stage IB Fallopian Tube Cancer", "AJCC stage IB fallopian tube cancer", "stage IB fallopian tube cancer AJCC v6", "stage IB fallopian tube cancer AJCC v7", "FIGO Stage IB Fallopian Tube Carcinoma", "Stage IB Fallopian Tube Cancer AJCC v7", "FIGO stage IB fallopian tube carcinoma", "Stage IB Fallopian Tube Cancer AJCC v6", "FIGO Stage IB Carcinoma of Fallopian Tube", "FIGO stage IB carcinoma of fallopian tube", "FIGO Stage IB Carcinoma of the Fallopian Tube", "FIGO stage IB carcinoma of the fallopian tube", "Stage IB Fallopian Tube Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Fallopian Tube Cancer AJCC v6 and v7", "shortest_name_length": 30}
{"curie": "MONDO:0013305", "names": ["DFNA51", "autosomal dominant deafness 51", "deafness, autosomal dominant 51", "DEAFNESS, AUTOSOMAL DOMINANT 51", "deafness, autosomal dominant type 51", "CHROMOSOME 9q21.11 DUPLICATION SYNDROME", "chromosome 9q21.11 duplication syndrome", "chromosome 9Q21.11 Duplication syndrome", "autosomal dominant nonsyndromic deafness 51", "autosomal dominant nonsyndromic hearing loss 51", "autosomal dominant nonsyndromic deafness type 51"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 51", "shortest_name_length": 6}
{"curie": "MONDO:0018428", "names": ["Del(9)(q31.1q31.3)", "monosomy 9q31.1q31.3", "9q31.1q31.3 microdeletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "9q31.1q31.3 microdeletion syndrome", "shortest_name_length": 18}
{"curie": "UMLS:C5556433", "names": ["p53-Mutant Endometrial Endometrioid Carcinoma", "p53-Mutant Endometrial Endometrioid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "p53-Mutant Endometrial Endometrioid Adenocarcinoma", "shortest_name_length": 45}
{"curie": "UMLS:C0005136", "names": ["Berry aneurysm", "BERRY ANEURYSM", "berry aneurysm", "Berry Aneurysm", "Aneurysm, Berry", "Berry Aneurysms", "berry aneurysms", "Aneurysms, Berry", "Saccular aneurysm", "Saccular Aneurysm", "Berry aneurysm disorder", "Berry aneurysm (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Berry Aneurysm", "shortest_name_length": 14}
{"curie": "UMLS:C4725602", "names": ["Refractory Chronic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Chronic Leukemia", "shortest_name_length": 27}
{"curie": "MONDO:0004647", "names": ["CIS", "Preinvasive", "Cancer in situ", "carcinoma situ", "stage 0 disease", "carcinoma in-situ", "carcinoma in situ", "Carcinoma in-situ", "in-situ carcinoma", "CARCINOMA IN SITU", "Carcinoma in situ", "in situ carcinoma", "Carcinoma in Situ", "Carcinoma In Situ", "Preinvasive Cancer", "Preinvasive Carcinoma", "Carcinoma in situ NOS", "Non-invasive carcinoma", "Carcinoma, Preinvasive", "Carcinoma in situ, NOS", "Non-invasive Carcinoma", "non-invasive carcinoma", "Carcinoma in situ tumor", "CIS - Carcinoma in situ", "Carcinoma in situ tumour", "intraepithelial carcinoma", "Intraepithelial carcinoma", "Intraepithelial Carcinoma", "Carcinoma, Intraepithelial", "Carcinoma in situ morphology", "Carcinoma in situ (disorder)", "carcinoma in situ (diagnosis)", "CARCINOMA, IN SITU, MALIGNANT", "carcinoma, in situ, malignant", "Intraepithelial carcinoma, NOS", "Carcinoma in situ, unspecified", "Carcinoma in situ, site unspecified", "Epithelial Tumor, In situ, Malignant", "epithelial tumor, in situ, malignant", "Carcinoma in situ (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "in situ carcinoma", "shortest_name_length": 3}
{"curie": "UMLS:C1960675", "names": ["Long-chain fatty acid transport deficiency", "Long-chain fatty acid transport deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Long-chain fatty acid transport deficiency", "shortest_name_length": 42}
{"curie": "UMLS:C0796563", "names": ["local cancer", "Local Cancer", "Localized Cancer", "Localized Malignancy", "Localized Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized Malignant Neoplasm", "shortest_name_length": 12}
{"curie": "MONDO:0018474", "names": ["Del(13)(q12.3)", "monosomy 13q12.3", "13q12.3 microdeletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "13q12.3 microdeletion syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C0751751", "names": ["Neonatal Citrullinemia", "neonatal citrullinemia", "Neonatal Citrullinemias", "Citrullinemia, Neonatal", "neonatal citrullinemia (diagnosis)", "Argininosuccinic Acid Synthetase Deficiency, Complete", "Deficiency, Argininosuccinic Acid Synthetase, Complete", "Complete Argininosuccinic Acid Synthetase Deficiency Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Argininosuccinic Acid Synthetase Deficiency, Complete", "shortest_name_length": 22}
{"curie": "UMLS:C3898765", "names": ["Infective Keratitis", "Infective keratitis", "Infectious Keratitis", "Infectious keratitis", "Keratitis caused by infection", "Keratitis caused by infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Keratitis caused by infection", "shortest_name_length": 19}
{"curie": "MONDO:0005433", "names": ["Alcohol withdrawal", "withdrawal alcohol", "ALCOHOL WITHDRAWAL", "alcohol withdrawal", "Alcohol Withdrawal", "alcohol withdrawals", "withdrawal; alcohol", "alcohol; withdrawal", "withdrawal state; alcohol", "alcohol; withdrawal state", "Alcohol withdrawal syndrome", "ALCOHOL WITHDRAWAL SYNDROME", "alcohol withdrawal syndrome", "alcohol syndrome withdrawal", "alcohol syndromes withdrawal", "alcohol; withdrawal syndrome", "syndrome; alcohol withdrawal", "alcohol withdrawal (diagnosis)", "Alcohol withdrawal syndrome (disorder)", "intoxication; alcohol, withdrawal state", "Alcohol withdrawal syndrome or symptoms", "Alcohol abstinence syndrome or symptoms", "alcohol; intoxication, withdrawal state", "alcohol; abstinence symptoms or syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alcohol withdrawal", "shortest_name_length": 18}
{"curie": "MONDO:0002043", "names": ["Ectropion", "Extropion", "ectropion", "extropion", "ECTROPION", "ectropions", "Ectropions", "Ectropion NOS", "Ectropion, NOS", "everted margin", "everted eyelid", "Everted margin", "Eyelid everted", "Everted eyelid", "Eyelid eversion", "Eyelid ectropion", "ectropion eyelids", "eyelid; ectropion", "Eyelid folded out", "ectropion; eyelid", "Eyelid turned out", "ectropion of eyelid", "Ectropion of eyelid", "ectropion (disease)", "Eyelashes turned out", "Eyelid turned outward", "ectropion (diagnosis)", "ectropion was observed", "Eversion of the eyelid", "Ectropion, unspecified", "ectropion (physical finding)", "Ectropion of eyelid (disorder)", "Unspecified ectropion of eyelid", "Everted margin (morphologic abnormality)", "Unspecified ectropion of unspecified eye, unspecified eyelid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectropion", "shortest_name_length": 9}
{"curie": "MONDO:0011545", "names": ["ENFL3", "nocturnal frontal lobe epilepsy 3", "epilepsy, nocturnal frontal lobe, 3", "EPILEPSY, NOCTURNAL FRONTAL LOBE, 3", "epilepsy, nocturnal frontal lobe, type 3", "Epilepsy, Nocturnal Frontal Lobe, Type 3", "autosomal dominant nocturnal frontal lobe epilepsy 3", "autosomal dominant nocturnal frontal lobe epilepsy type 3", "CHRNB2 autosomal dominant nocturnal frontal lobe epilepsy", "autosomal dominant nocturnal frontal lobe epilepsy caused by mutation in CHRNB2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nocturnal frontal lobe epilepsy 3", "shortest_name_length": 5}
{"curie": "MONDO:0002788", "names": ["PCP", "Papillary craniopharyngioma", "Papillary Craniopharyngioma", "papillary craniopharyngioma", "craniopharyngioma, papillary", "Papillary Craniopharyngiomas", "Craniopharyngioma, Papillary", "Craniopharyngioma, papillary", "Craniopharyngiomas, Papillary", "Papillary Rathke's Pouch tumor", "papillary Rathke's pouch tumor", "Papillary Rathke's Pouch Tumor", "Papillary Rathke Pouch Neoplasm", "papillary Rathke pouch neoplasm", "papillary Rathke's pouch neoplasm", "papillary tumor of Rathke's pouch", "Papillary Rathke's Pouch Neoplasm", "Papillary Tumor of Rathke's Pouch", "papillary neoplasm of Rathke's pouch", "Papillary Neoplasm of Rathke's Pouch", "papillary craniopharyngioma (morphologic abnormality)", "craniopharyngioma, papillary (morphologic abnormality)", "Craniopharyngioma, papillary (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papillary craniopharyngioma", "shortest_name_length": 3}
{"curie": "MONDO:0013558", "names": ["HPS6", "Hermansky-Pudlak syndrome 6", "HERMANSKY-PUDLAK SYNDROME 6", "Hermansky-Pudlak Syndrome 6", "HPS6 Hermansky-Pudlak syndrome", "Hermansky-Pudlak syndrome type 6", "Hermansky-Pudlak syndrome caused by mutation in HPS6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hermansky-Pudlak syndrome 6", "shortest_name_length": 4}
{"curie": "MONDO:0010200", "names": ["WD", "WND", "Wnd", "Wilson Disease", "Gowers' chorea", "WILSON DISEASE", "Wilson disease", "disease wilson", "wilson disease", "Disease;Wilsons", "wilsons disease", "diseases wilson", "Wilsons disease", "Wilsons Disease", "Pseudosclerosis", "disease wilsons", "Wilson's disease", "disease wilson's", "Wilson's Disease", "wilson's disease", "familial hepatitis", "Strümpell-Westphal", "Westphal-Strümpell", "WD - Wilson's disease", "wilsons disease liver", "Copper storage disease", "Kinnier Wilson Disease", "Kinnier-Wilson disease", "Copper Storage Disease", "Kinnier-Wilson Disease", "Storage Disease, Copper", "HEPATIC WILSONS DISEASE", "Kinnier-Wilson Diseases", "Disease, Copper Storage", "Copper Storage Diseases", "Diseases, Copper Storage", "Cerebral pseudosclerosis", "Cerebral Pseudosclerosis", "cerebral pseudosclerosis", "Diseases, Kinnier-Wilson", "Cerebral Pseudoscleroses", "Storage Diseases, Copper", "Westphal pseudosclerosis", "Pseudosclerosis, Cerebral", "Pseudoscleroses, Cerebral", "neurohepatic degeneration", "Neurohepatic Degeneration", "Neurohepatic degeneration", "Degeneration, Neurohepatic", "Neurohepatic Degenerations", "Westphal Strumpell disease", "Westphal Strumpell Syndrome", "Wilson's disease (disorder)", "Wilson; disease or syndrome", "Hepatocerebral Degeneration", "hepatocerebral degeneration", "Westphal-Strumpell syndrome", "Hepatocerebral degeneration", "Degenerations, Neurohepatic", "Westphal-Strumpell Syndrome", "Wilson's disease (diagnosis)", "Degeneration, Hepatocerebral", "Westphal-Strumpell Syndromes", "Hepatocerebral Degenerations", "hepatolenticular Degeneration", "HEPATOLENTICULAR DEGENERATION", "hepatolenticular degeneration", "Hepatolenticular Degeneration", "Degenerations, Hepatocerebral", "Hepatolenticular degeneration", "degeneration; hepatolenticular", "Hepato-lenticular degeneration", "hepato-lenticular degeneration", "hepatolenticular; degeneration", "Degeneration, Hepatolenticular", "Hepato Neurologic Wilson Disease", "Hepato-Neurologic Wilson Disease", "Wilson Disease, Hepato-Neurologic", "Hepato-Neurologic Wilson Diseases", "Wilson Diseases, Hepato-Neurologic", "Diseases, Hepato-Neurologic Wilson", "Progressive lenticular degeneration", "Progressive Lenticular Degeneration", "WESTPHAL-STRUEMPELL PSEUDOSCLEROSIS", "lenticular degeneration; progressive", "Lenticular Degeneration, Progressive", "Degeneration, Progressive Lenticular", "LENTICULAR DEGENERATION, PROGRESSIVE", "Hepatolenticular Degeneration Syndrome", "Hepatolenticular degeneration syndrome", "Westphal-Strumpell syndrome (disorder)", "Hepatolenticular Degeneration Syndromes", "Degeneration Syndrome, Hepatolenticular", "Syndrome, Hepatolenticular Degeneration", "Syndromes, Hepatolenticular Degeneration", "Pseudosclerotic type of Wilson's disease", "Degeneration Syndromes, Hepatolenticular", "Westphal-Strumpell cerebral pseudosclerosis", "Westphal-Strumpell form of Wilson's disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wilson disease", "shortest_name_length": 2}
{"curie": "UMLS:C4528756", "names": ["Stage IIIA Rectal Cancer", "Stage IIIA Rectal Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Rectal Cancer AJCC v8", "shortest_name_length": 24}
{"curie": "MONDO:0030433", "names": ["CMT2FF", "Charcot-Marie-Tooth neuropathy", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2FF", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2FF", "Charcot-Marie-Tooth disease, axonal, type 2FF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease, axonal, type 2FF", "shortest_name_length": 6}
{"curie": "UMLS:C4727683", "names": ["Advanced Oral Cavity Squamous Cell Cancer", "Advanced Oral Cavity Squamous Cell Carcinoma", "Advanced Squamous Cell Carcinoma of the Oral Cavity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Oral Cavity Squamous Cell Carcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0021148", "names": ["Gynecologic Tumor", "gynecologic tumor", "Neoplasm;genital;F", "Gynecologic Neoplasm", "gynecologic neoplasm", "Gynecologic Neoplasms", "Neoplasm, Gynecologic", "Neoplasms, Gynecologic", "Female Genital Neoplasm", "Genital Neoplasm, Female", "Female Genital Neoplasms", "Neoplasm, Female Genital", "Neoplasms, Female Genital", "Genital Neoplasms, Female", "female reproductive neoplasm", "Female reproductive neoplasm", "female neoplasm reproductive", "Tumor of female genital organs", "Tumour of female genital organs", "female reproductive organ tumor", "female reproductive system tumor", "Neoplasm of female genital organ", "Female reproductive neoplasm NOS", "Female Reproductive System Tumor", "female reproductive system cancer", "tumor of female reproductive system", "Female reproductive system neoplasm", "Tumor of Female Reproductive System", "Female Reproductive System Neoplasm", "female reproductive system neoplasm", "neoplasm of the female genital system", "neoplasm of female reproductive organ", "neoplasm of female reproductive system", "Neoplasm of Female Reproductive System", "Female reproductive tract neoplasm NOS", "Tumor of the Female Reproductive System", "tumor of the female reproductive system", "Neoplasm of the Female Reproductive System", "neoplasm of the female reproductive system", "Neoplasm of female genital organ (disorder)", "female reproductive organ neoplasm (disease)", "female reproductive system neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "female reproductive system neoplasm", "shortest_name_length": 17}
{"curie": "UMLS:C4524728", "names": ["Pathologic Stage IC Gastroesophageal Junction Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IC Gastroesophageal Junction Adenocarcinoma AJCC v8", "shortest_name_length": 68}
{"curie": "MONDO:0014460", "names": ["ECTDS", "ectodermal dysplasia-short stature syndrome", "Ectodermal dysplasia short stature syndrome", "Ectodermal dysplasia-short stature syndrome", "ECTODERMAL DYSPLASIA/SHORT STATURE SYNDROME", "ectodermal dysplasia/short stature syndrome", "short stature-nail dysplasia-marginal palmoplantar keratoderma-oral hyperpigmentation syndrome", "nail and teeth abnormalities-marginal palmoplantar keratoderma-oral hyperpigmentation syndrome", "Nail and teeth abnormalities-marginal palmoplantar keratoderma-oral hyperpigmentation syndrome", "Short stature-nail dysplasia-marginal palmoplantar keratoderma-oral hyperpigmentation syndrome", "Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome", "Short stature, nail dysplasia, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome", "Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nail and teeth abnormalities-marginal palmoplantar keratoderma-oral hyperpigmentation syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0752304", "names": ["HIE", "Anoxic encephalopathy", "hypoxic ischemic brain injury", "Hypoxic ischemic brain injury", "Hypoxic ischaemic brain injury", "Hypoxic Ischemic Encephalopathy", "hypoxic ischemic encephalopathy", "Hypoxic-ischemic encephalopathy", "Ischemic Hypoxic Encephalopathy", "Hypoxic ischemic encephalopathy", "encephalopathy hypoxic-ischemic", "encephalopathy hypoxic ischemic", "hypoxic-ischemic encephalopathy", "Ischemic-Hypoxic Encephalopathy", "Hypoxic-Ischemic Encephalopathy", "Hypoxic ischaemic encephalopathy", "Encephalopathy, Hypoxic-Ischemic", "Hypoxic-ischaemic encephalopathy", "Encephalopathy, Hypoxic Ischemic", "Encephalopathy, Ischemic-Hypoxic", "Hypoxic-Ischemic Encephalopathies", "Ischemic-Hypoxic Encephalopathies", "Encephalopathies, Ischemic-Hypoxic", "Encephalopathies, Hypoxic-Ischemic", "Hypoxic ischemic encephalopathy [HIE]", "Hypoxic-ischemic encephalopathy (HIE)", "Hypoxic-ischemic encephalopathy (disorder)", "Hypoxic ischemic encephalopathy (disorder)", "hypoxic-ischemic encephalopathy (diagnosis)", "Hypoxic-ischemic encephalopathy, unspecified", "Hypoxic ischemic encephalopathy [HIE], unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypoxic-Ischemic Encephalopathy", "shortest_name_length": 3}
{"curie": "UMLS:C5555174", "names": ["Refractory Ovarian Seromucinous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Ovarian Seromucinous Carcinoma", "shortest_name_length": 41}
{"curie": "UMLS:C0340529", "names": ["Cardiac transplant disorder", "Transplanted Heart Complication", "complications of heart transplant", "Complications of heart transplant", "Complication of Transplanted Heart", "Complication of transplanted heart", "Complications of transplanted heart", "complications of heart transplant (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Complications of transplanted heart", "shortest_name_length": 27}
{"curie": "UMLS:C5555609", "names": ["Endometrial MLA", "Uterine Corpus MLA", "Endometrial Mesonephric-Like Adenocarcinoma", "Uterine Corpus Mesonephric-Like Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endometrial Mesonephric-Like Adenocarcinoma", "shortest_name_length": 15}
{"curie": "MONDO:0008516", "names": ["SD5", "SDTY5", "Syndactyly type 5", "syndactyly type 5", "syndactyly, type 5", "SYNDACTYLY, TYPE V", "Syndactyly, type v", "syndactyly, type V", "Syndactyly type 5 (disorder)", "syndactyly type 5 (diagnosis)", "Postaxial syndactyly with metacarpal synostosis", "postaxial syndactyly with metacarpal synostosis", "syndactyly with metacarpal and metatarsal fusion", "SYNDACTYLY WITH METACARPAL AND METATARSAL FUSION", "Syndactyly with metacarpal and metatarsal fusion", "syndactyly with associated metacarpal and metatarsal fusion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndactyly type 5", "shortest_name_length": 3}
{"curie": "UMLS:C1332473", "names": ["Benign Apocrine Tumor", "Benign Apocrine Neoplasm", "Benign Apocrine Skin Tumor", "Benign Apocrine Tumor of Skin", "Benign Apocrine Skin Neoplasm", "Benign Apocrine Neoplasm of Skin", "Benign Apocrine Tumor of the Skin", "Benign Apocrine Neoplasm of the Skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Apocrine Neoplasm", "shortest_name_length": 21}
{"curie": "MONDO:0024945", "names": ["animal Hepatitis", "Animal Hepatitis", "Hepatitis, Animal", "animal Hepatitides", "Animal Hepatitides", "Hepatitides, Animal", "Hepatitides, animal", "hepatitis, non-human animal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatitis, non-human animal", "shortest_name_length": 16}
{"curie": "MONDO:0005730", "names": ["Dictyocaulosis", "Dictyocauliases", "Dictyocauliasis", "Dictyocaulus Infection", "Dictyocaulus infection", "infection, Dictyocaulus", "Infection, Dictyocaulus", "Dictyocaulus Infections", "Infections, Dictyocaulus", "infections, Dictyocaulus", "Infection by Dictyocaulus, NOS", "Dictyocaulus infectious disease", "Infection caused by Dictyocaulus", "Dictyocaulus disease or disorder", "Dictyocaulus caused disease or disorder", "Infection caused by Dictyocaulus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dictyocaulus infectious disease", "shortest_name_length": 14}
{"curie": "UMLS:C4049314", "names": ["Vascular stent stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vascular stent stenosis", "shortest_name_length": 23}
{"curie": "UMLS:C1332148", "names": ["Acute Erythroid Leukemia in Remission", "Acute erythroid leukemia, in remission"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Erythroid Leukemia in Remission", "shortest_name_length": 37}
{"curie": "UMLS:C4055470", "names": ["Anaplastic Embryonal Rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anaplastic Embryonal Rhabdomyosarcoma", "shortest_name_length": 37}
{"curie": "MONDO:0020307", "names": ["Panayiotopoulos syndrome", "Panayiotopoulos Syndrome", "Early-onset benign childhood occipital epilepsy", "early-onset benign childhood occipital epilepsy", "Benign childhood occipital epilepsy Panayiotopoulos type", "benign childhood occipital epilepsy, Panayiotopoulos type", "Benign childhood occipital epilepsy, Panayiotopoulos type", "Benign occipital epilepsy of childhood - early onset variant", "Benign occipital epilepsy of childhood - early onset variant (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign childhood occipital epilepsy, Panayiotopoulos type", "shortest_name_length": 24}
{"curie": "UMLS:C5669878", "names": ["Diffuse Midline Glioma, EGFR-Mutant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse Midline Glioma, EGFR-Mutant", "shortest_name_length": 35}
{"curie": "UMLS:C1262170", "names": ["herpes dermatitis", "Herpes dermatitis", "eczema; herpes, eczema herpeticum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Herpes dermatitis", "shortest_name_length": 17}
{"curie": "UMLS:C1335173", "names": ["Ovarian Non-Neoplastic Disease", "Ovarian Non-Neoplastic Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Non-Neoplastic Disorder", "shortest_name_length": 30}
{"curie": "MONDO:0012396", "names": ["EIHI", "HHF7", "MCT1 Hyperinsulinism", "MCT1 hyperinsulinism", "Exercise-induced hyperinsulinism", "exercise-induced hyperinsulinism", "Exercise-induced Hyperinsulinism", "familial hyperinsulinemic hypoglycemia 7", "hyperinsulinemic hypoglycemia familial 7", "hyperinsulinism due to SLC16A1 deficiency", "Hyperinsulinism due to SLC16A1 deficiency", "Hyperinsulinemic hypoglycemia, familial, 7", "hyperinsulinemic hypoglycemia, familial, 7", "HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 7", "Exercise-induced hyperinsulinism (disorder)", "monocarboxylate transporter 1 hyperinsulinism", "Monocarboxylate Transporter 1 Hyperinsulinism", "hyperinsulinemic hypoglycemia exercise-induced", "exercise induced hyperinsulinemic hypoglycemia", "Exercise-induced hyperinsulinemic hypoglycemia", "exercise-induced hyperinsulinemic hypoglycemia", "Hyperinsulinemic hypoglycemia, exercise-induced", "HYPERINSULINEMIC HYPOGLYCEMIA, EXERCISE-INDUCED", "hyperinsulinemic hypoglycemia, familial, type 7", "hyperinsulinemic hypoglycemia, exercise-induced", "Exercise-induced hyperinsulinaemic hypoglycaemia", "hyperinsulinism due to monocarboxylate transporter 1 deficiency", "Hyperinsulinism due to monocarboxylate transporter 1 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exercise-induced hyperinsulinism", "shortest_name_length": 4}
{"curie": "UMLS:C3502492", "names": ["Microcephaly with Chorioretinopathy, Autosomal Recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Microcephaly with Chorioretinopathy, Autosomal Recessive", "shortest_name_length": 56}
{"curie": "UMLS:C0948807", "names": ["Hepatic impairment", "hepatic impairment"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatic impairment", "shortest_name_length": 18}
{"curie": "UMLS:C4527330", "names": ["Recurrent Testicular Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Testicular Lymphoma", "shortest_name_length": 29}
{"curie": "UMLS:C1389062", "names": ["Cartilage atrophy", "atrophy; cartilage", "cartilage; atrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cartilage atrophy", "shortest_name_length": 17}
{"curie": "MONDO:0001061", "names": ["pylorus cancer", "cancer of pylorus", "Ca pylorus - stomach", "malignant tumor of pylorus", "malignant pylorus neoplasm", "Malignant Pylorus Neoplasm", "Malignant tumor of pylorus", "Malignant tumour of pylorus", "malignant neoplasm of pylorus", "Malignant neoplasm of pylorus", "Malignant neoplasm of prepylorus", "malignant neoplasm of Prepylorus", "Malignant neoplasm of Prepylorus", "Malignant neoplasm of Pyloric canal", "Malignant neoplasm of pyloric canal", "malignant tumor of pylorus of stomach", "Malignant tumor of pylorus (disorder)", "Malignant neoplasm of pylorus of stomach", "malignant neoplasm of pylorus of stomach", "malignant neoplasm of pylorus of stomach (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pylorus cancer", "shortest_name_length": 14}
{"curie": "UMLS:C5205659", "names": ["Locally Advanced Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Breast Carcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C0024043", "names": ["Low T3 syndrome", "Low T3 Syndrome", "Low Triiodothyronine Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low T3 Syndrome", "shortest_name_length": 15}
{"curie": "UMLS:C0349555", "names": ["VIN II", "vin ii", "VAIN 2", "VAIN II", "Grade 2 VAIN", "moderate vaginal dysplasia", "Moderate vaginal dysplasia", "moderate vaginal dysplasia (diagnosis)", "Vaginal intraepithelial neoplasia grade 2", "Vaginal Intraepithelial Neoplasia Grade 2", "Grade 2 Vaginal Intraepithelial Neoplasia", "Grade II Vaginal Intraepithelial Neoplasia", "Vaginal intraepithelial neoplasia grade II", "VAIN - Vaginal intraepithelial neoplasia 2", "vagina; intraepithelial neoplasia, grade II", "Intraepithelial Neoplasia of Vagina Grade 2", "neoplasia; intraepithelial, vagina, grade II", "Intraepithelial Neoplasia of the Vagina Grade 2", "Vaginal intraepithelial neoplasia [VAIN], grade II", "Vaginal intraepithelial neoplasia grade 2 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal intraepithelial neoplasia grade 2", "shortest_name_length": 6}
{"curie": "MONDO:0017317", "names": ["phakomatosis pigmentokeratotica", "Phacomatosis pigmentokeratotica", "Phakomatosis pigmentokeratotica", "Phakomatosis pigmentokeratotica (disorder)", "organoid nevus with sebaceous differentiation, a speckled-lentiginous nevus, and other associated anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phakomatosis pigmentokeratotica", "shortest_name_length": 31}
{"curie": "UMLS:C0280423", "names": ["Adult T-cell lymphoma/leukemia stage I", "Adult T-Cell Lymphoma/Leukemia Stage I", "Stage I Adult T-Cell Leukemia/Lymphoma", "Stage I Adult T-Cell Lymphoma/Leukemia", "stage I adult T-cell leukemia/lymphoma", "adult T-cell leukemia/lymphoma, stage I", "Adult T-cell lymphoma/leukaemia stage I", "Ann Arbor Stage I Adult T-Cell Leukemia/Lymphoma", "Stage I HTLV-1 Associated Adult T-Cell Lymphoma/Leukemia", "HTLV-1 Associated Adult T-Cell Lymphoma/Leukemia Stage I", "stage I HTLV-I associated adult T-cell leukemia/lymphoma", "HTLV-I associated adult T-cell leukemia/lymphoma, stage I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult T-cell lymphoma/leukemia stage I", "shortest_name_length": 38}
{"curie": "UMLS:C0403766", "names": ["phimosis", "Phimosis", "acquired phimosis", "Acquired Phimosis", "Acquired phimosis", "Phimosis;acquired", "Acquired phimosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired phimosis", "shortest_name_length": 8}
{"curie": "MONDO:0006409", "names": ["gastric signet Ring cell adenocarcinoma", "Signet-ring cell adenocarcinoma gastric", "Signet Ring Cell Gastric Adenocarcinoma", "signet ring cell gastric adenocarcinoma", "Signet Ring Cell Stomach Adenocarcinoma", "signet Ring cell stomach adenocarcinoma", "Gastric Signet Ring Cell Adenocarcinoma", "gastric signet ring cell adenocarcinoma", "Gastric Signet-Ring Cell Adenocarcinoma", "signet ring cell carcinoma of the stomach", "signet Ring cell adenocarcinoma of stomach", "Signet Ring Cell Adenocarcinoma of Stomach", "signet Ring cell adenocarcinoma of the stomach", "Signet Ring Cell Adenocarcinoma of the Stomach", "Signet Ring cell adenocarcinoma of the stomach", "Poorly cohesive carcinoma, including signet ring cell carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "signet ring cell gastric adenocarcinoma", "shortest_name_length": 39}
{"curie": "UMLS:C0278664", "names": ["stage IV adult soft tissue sarcoma", "Stage IV adult soft tissue sarcoma", "adult soft tissue sarcoma, stage IV", "soft tissue sarcoma, adult, stage IV", "sarcoma, adult soft tissue, stage IV", "Metastatic Adult Soft Tissue Sarcoma", "Stage IV Adult Sarcoma of Soft Tissue", "sarcoma, adult soft tissue, metastatic", "Stage IV Adult Sarcoma of the Soft Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV adult soft tissue sarcoma", "shortest_name_length": 34}
{"curie": "MONDO:0010614", "names": ["Cgh", "hCG", "CGH", "HCG", "HTC2", "Hypertrichosis universalis", "Congenital generalized hypertrichosis", "Congenital generalised hypertrichosis", "HYPERTRICHOSIS, CONGENITAL GENERALIZED", "Congenital, generalized hypertrichosis", "Congenital, generalised hypertrichosis", "hypertrichosis, congenital generalized", "Hypertrichosis, Congenital Generalized", "Macias Flores-Garcia Cruz-Rivera syndrome", "Macias-Flores Garcia-Cruz Rivera syndrome", "hypertrichosis congenital generalized X-linked", "X-linked congenital generalized hypertrichosis", "Hypertrichosis congenital generalized X-linked", "X-linked congenital generalised hypertrichosis", "Congenital generalized hypertrichosis (disorder)", "chromosome Xq27.1 Interchromosomal insertion syndrome", "CHROMOSOME Xq27.1 INTERCHROMOSOMAL INSERTION SYNDROME", "chromosome Xq27.1 interchromosomal insertion syndrome", "Congenital generalized hypertrichosis Macias-Flores type", "Congenital generalised hypertrichosis Macias-Flores type", "X-linked congenital generalized hypertrichosis (disorder)", "Congenital generalized hypertrichosis, Macias-Flores type", "congenital generalized hypertrichosis, Macias-Flores type", "hypertrichosis, congenital generalized, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked congenital generalized hypertrichosis", "shortest_name_length": 3}
{"curie": "MONDO:0017499", "names": ["radio-ulnar terminal transverse meromelia, bilateral", "congenital absence of both forearm and hand, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital absence of both forearm and hand, bilateral", "shortest_name_length": 52}
{"curie": "MONDO:0010937", "names": ["ISOPROTERENOL-MEDIATED VASODILATATION", "isoproterenol-mediated vasodilatation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isoproterenol-mediated vasodilatation", "shortest_name_length": 37}
{"curie": "MONDO:0042961", "names": ["Sacral hemangiomas multiple congenital abnormalities", "sacral hemangiomas multiple congenital abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sacral hemangiomas multiple congenital abnormalities", "shortest_name_length": 52}
{"curie": "UMLS:C4285714", "names": ["Renal graft infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal graft infection", "shortest_name_length": 21}
{"curie": "UMLS:C5235845", "names": ["Advanced Ureter Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Ureter Urothelial Carcinoma", "shortest_name_length": 36}
{"curie": "UMLS:C0281857", "names": ["Genital Fistula", "Genital Tract Fistula"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Genital Tract Fistula", "shortest_name_length": 15}
{"curie": "MONDO:0013214", "names": ["PBAM", "PBAM1", "Bile Acid Malabsorption, Primary", "BILE ACID MALABSORPTION, PRIMARY", "bile acid malabsorption, primary", "Bile acid malabsorption, primary, 1", "BILE ACID MALABSORPTION, PRIMARY, 1", "bile acid malabsorption, primary, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bile acid malabsorption, primary, 1", "shortest_name_length": 4}
{"curie": "UMLS:C1306792", "names": ["red man", "mans red", "Red man syndrome", "red man syndrome", "RED MAN SYNDROME", "Red Man Syndrome", "red mans syndrome", "Red man's syndrome", "red man's syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Red man syndrome", "shortest_name_length": 7}
{"curie": "MONDO:0013288", "names": ["AGM3", "agammaglobulinemia 3", "CD79A autosomal agammaglobulinemia", "AGAMMAGLOBULINEMIA 3, AUTOSOMAL RECESSIVE", "agammaglobulinemia 3, autosomal recessive", "autosomal agammaglobulinemia caused by mutation in CD79A", "agammaglobulinemia, autosomal recessive, due to Cd79A defect", "AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO CD79A DEFECT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "agammaglobulinemia 3, autosomal recessive", "shortest_name_length": 4}
{"curie": "MONDO:0020678", "names": ["SNHL", "Perceptive deafness", "perceptive deafness", "sensory hearing loss", "DEAFNESS, PERCEPTIVE", "Sensory hearing loss", "deafness; perception", "central hearing loss", "perception; deafness", "Deafness;sensoneural", "neurosensory deafness", "Neurosensory Deafness", "Neurosensory deafness", "Deafness Neurosensory", "Sensoryneural Deafness", "Sensorineural Deafness", "Sensorineural deafness", "Neuro sensory deafness", "DEAFNESS SENSORINEURAL", "sensorineural deafness", "inner ear hearing loss", "Deafness, Neurosensory", "Deafness Sensorineural", "sensory neuro deafness", "Perceptive hearing loss", "Deafness, sensorineural", "High frequency deafness", "Sensory-neural deafness", "Deafness, Sensoryneural", "Neurosensory Deafnesses", "sensori-neural deafness", "Sensoryneural Deafnesses", "Deafnesses, Neurosensory", "Hearing loss, perceptive", "HEARING DISORDER, NEURAL", "PD - Perceptive deafness", "Perceptive deafness, NOS", "Deafnesses, Sensoryneural", "Sensorineural deafness NOS", "Sensorineural Hearing Loss", "sensorineural hearing loss", "Sensorineural hearing loss", "HEARING LOSS SENSORINEURAL", "hearing loss sensorineural", "Perceptive hearing loss NOS", "Sensory-neural hearing loss", "high-frequency hearing loss", "High Frequency Hearing Loss", "Hearing loss, sensorineural", "Hearing Loss, Sensorineural", "hearing loss sensori neural", "Perceptive hearing loss, NOS", "sensorineural hearing losses", "SND - Sensorineural deafness", "HEARING DISORDER RETROCOCHLEAR", "Sensorineural hearing loss, NOS", "HEARING DISORDER, SENSORINEURAL", "Sensorineural deafness syndrome", "Sensorineural hearing impairment", "SNHL - Sensorineural hearing loss", "Hearing impairment, sensorineural", "sensorineural hearing loss disorder", "Perceptive hearing loss or deafness", "hearing; loss, sensorineural disorder", "Sensorineural hearing loss (disorder)", "Sensorineural Hearing Loss (disorder)", "loss; hearing, sensorineural disorder", "sensorineural hearing loss (diagnosis)", "Unspecified sensorineural hearing loss", "Sensorineural hearing loss, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sensorineural hearing loss disorder", "shortest_name_length": 4}
{"curie": "MONDO:0004431", "names": ["joint bleed", "hemarthrosis", "HEMARTHROSIS", "Hemarthroses", "Hemarthrosis", "hemarthroses", "haemarthrosis", "HAEMARTHROSIS", "Haemarthrosis", "JOINT BLEEDING", "bleeding joint", "Joint bleeding", "joint bleeding", "bleeding joints", "Joint hemorrhage", "Hemarthrosis, NOS", "hemorrhage; joint", "Joint haemorrhage", "joint; hemorrhage", "Haemarthrosis, NOS", "Bleeding into joint", "Hemarthrosis of hand", "hemarthrosis of hand", "Shoulder hemarthrosis", "Hemarthrosis, shoulder", "Shoulder haemarthrosis", "hemarthrosis was found", "Hemarthrosis of forearm", "Bleeding within a joint", "hemarthrosis of forearm", "Hemarthrosis (disorder)", "Hemarthrosis of the hand", "hemarthrosis of the hand", "hemarthrosis (diagnosis)", "Hemarthrosis of shoulder", "hemarthrosis of shoulder", "Intraarticular hemorrhage", "Haemarthrosis of shoulder", "hemarthrosis of lower leg", "Hemarthrosis of lower leg", "Hemarthrosis of upper arm", "hemarthrosis of upper arm", "Intraarticular haemorrhage", "hemarthrosis of the forearm", "hemarthrosis involving hand", "Hemarthrosis of the forearm", "Hemarthrosis involving hand", "Spontaneous joint hemorrhage", "hemarthrosis of the lower leg", "hemarthrosis of the upper arm", "Hemarthrosis of the lower leg", "Hemarthrosis of the upper arm", "Spontaneous joint haemorrhage", "Hemarthrosis, shoulder region", "Haemarthrosis, shoulder region", "Hemarthrosis of shoulder joint", "Hemarthrosis involving forearm", "Hemarthrosis, site unspecified", "hemarthrosis involving forearm", "Haemarthrosis, site unspecified", "haemarthrosis of shoulder joint", "hemarthrosis of shoulder region", "hemarthrosis (physical finding)", "Haemarthrosis of shoulder joint", "Hemarthrosis of shoulder region", "hemarthrosis involving lower leg", "Hemarthrosis involving upper arm", "Haemarthrosis of shoulder region", "hemarthrosis involving upper arm", "Hemarthrosis involving lower leg", "hemarthrosis of ankle and/or foot", "Hemarthrosis of ankle and/or foot", "hemarthrosis of the ankle and foot", "Hemarthrosis of the ankle and foot", "Haemarthrosis of the ankle and foot", "haemarthrosis of the ankle and foot", "Hemarthrosis of the shoulder region", "hemarthrosis of the shoulder region", "Hemarthrosis involving ankle and foot", "Hemarthrosis of the ankle and/or foot", "hemarthrosis of the ankle and/or foot", "hemarthrosis involving ankle and foot", "Hemarthrosis involving shoulder region", "hemarthrosis involving shoulder region", "Hemarthrosis of shoulder region (disorder)", "hemarthrosis of the pelvic region and thigh", "Hemarthrosis of the pelvic region and thigh", "hemarthrosis of shoulder region (diagnosis)", "Haemarthrosis of the pelvic region and thigh", "haemarthrosis of the pelvic region and thigh", "hemarthrosis involving pelvic region and thigh", "Hemarthrosis involving pelvic region and thigh"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemarthrosis", "shortest_name_length": 11}
{"curie": "UMLS:C1335732", "names": ["Region 17p13 Allelic Loss Associated Medulloblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Region 17p13 Allelic Loss Associated Medulloblastoma", "shortest_name_length": 52}
{"curie": "UMLS:C4525096", "names": ["Stage IVB Colorectal Cancer AJCC v8", "Stage IVB Colorectal Carcinoma AJCC v8", "Stage IVB Colorectal (Colon or Rectal) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Colorectal Cancer AJCC v8", "shortest_name_length": 35}
{"curie": "MONDO:0100505", "names": ["food dermatitis", "Food allergy dermatitis", "dermatitis due to consumed food", "Dermatitis due to ingested food", "Dermatitis caused by ingested food", "dermatitis due to food taken internally", "Dermatitis due to food taken internally", "Dermatitis due to Food taken Internally", "dermatitis due to consumed food (diagnosis)", "Dermatitis caused by ingested food (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "food dermatitis", "shortest_name_length": 15}
{"curie": "MONDO:0001608", "names": ["Vagus Nerve Tumor", "Vagus nerve tumor", "vagus nerve tumor", "Vagus Nerve Tumors", "Vagus nerve tumors", "Tumor of Vagus Nerve", "Vagus Nerve Neoplasm", "Vagus nerve neoplasm", "vagus nerve neoplasm", "tumor of Vagus nerve", "tumor of vagus nerve", "Vagus Nerve Neoplasms", "Vagus nerve neoplasms", "Neoplasm of vagus nerve", "Neoplasm of Vagus Nerve", "neoplasm of Vagus nerve", "neoplasm of vagus nerve", "tumor of the Vagus nerve", "Xth Cranial Nerve Tumors", "Tumor of the Vagus Nerve", "Xth cranial nerve tumors", "tenth cranial nerve tumor", "Tenth Cranial Nerve Tumor", "Tenth Cranial Nerve Tumors", "tenth cranial nerve tumors", "Neoplasm of the Vagus Nerve", "Xth cranial nerve neoplasms", "neoplasm of the Vagus nerve", "Xth Cranial Nerve Neoplasms", "tumor of tenth cranial nerve", "Tumor of Tenth Cranial Nerve", "tenth cranial nerve neoplasm", "Tenth Cranial Nerve Neoplasm", "Tenth Cranial Nerve Neoplasms", "tenth cranial nerve neoplasms", "vagus nerve neoplasm (disease)", "neoplasm of tenth cranial nerve", "Neoplasm of Tenth Cranial Nerve", "tumor of the tenth cranial nerve", "Tumor of the Tenth Cranial Nerve", "Neoplasm of vagus nerve (disorder)", "neoplasm of the tenth cranial nerve", "Neoplasm of the Tenth Cranial Nerve", "neoplasm of tenth cranial nerve (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vagus nerve neoplasm", "shortest_name_length": 17}
{"curie": "MONDO:0016267", "names": ["endometrial undifferentiated carcinoma", "body of uterus undifferentiated carcinoma", "undifferentiated carcinoma of the corpus uteri"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "undifferentiated carcinoma of the corpus uteri", "shortest_name_length": 38}
{"curie": "UMLS:C2751297", "names": ["STHAG6", "Tooth Agenesis, Selective, 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tooth Agenesis, Selective, 6", "shortest_name_length": 6}
{"curie": "MONDO:0001403", "names": ["labium majus cancer", "labium majora cancer", "cancer of labium majora", "Malignant Labia Majora Tumor", "malignant labia majora tumor", "malignant tumor of labia majora", "Malignant Tumor of Labia Majora", "malignant labia majora neoplasm", "Malignant Labia Majora Neoplasm", "malignant tumor of Labia Majora", "malignant labium majora neoplasm", "Malignant neoplasm of labium majus", "Malignant Neoplasm of Labia Majora", "Malignant neoplasm of labia majora", "malignant neoplasm of labia majora", "malignant neoplasm of labium majora", "Malignant Tumor of the Labia Majora", "malignant tumor of the labia majora", "Malignant Neoplasm of the Labia Majora", "malignant neoplasm of the labia majora", "Malignant neoplasm of labia majora (disorder)", "malignant neoplasm of labia majora (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "labium majus cancer", "shortest_name_length": 19}
{"curie": "MONDO:0011709", "names": ["SHFM5", "split hand-foot malformation 5", "Split-Hand/Foot Malformation 5", "Split-Hand-Foot Malformation 5", "split-hand/foot malformation 5", "SPLIT-HAND/FOOT MALFORMATION 5", "split hand-foot malformation type 5", "Split-Hand/Foot Malformation Type 5", "split-hand/foot malformation type 5", "SPLIT-HAND/FOOT MALFORMATION 5 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "split hand-foot malformation 5", "shortest_name_length": 5}
{"curie": "UMLS:C5203822", "names": ["Endometrioid Tumor, Variant with Squamous Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endometrioid Tumor, Variant with Squamous Differentiation", "shortest_name_length": 57}
{"curie": "UMLS:C4521802", "names": ["Stage II Anal Cancer", "Stage II Anal Cancer AJCC v8", "Stage II Anal Carcinoma AJCC v8", "Stage II Anal Canal and Perianal (Anal Margin) Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Anal Cancer AJCC v8", "shortest_name_length": 20}
{"curie": "UMLS:C1709873", "names": ["Relapsed Anterior Pituitary Tumor", "Recurrent Anterior Pituitary Tumor", "Relapsed Anterior Pituitary Neoplasm", "Recurrent Anterior Pituitary Neoplasm", "Recurrent Tumor of Anterior Pituitary", "Relapsed Neoplasm of Anterior Pituitary", "Relapsed Anterior Pituitary Gland Tumor", "Recurrent Anterior Pituitary Gland Tumor", "Recurrent Neoplasm of Anterior Pituitary", "Recurrent Tumor of the Anterior Pituitary", "Relapsed Tumor of Anterior Pituitary Gland", "Relapsed Anterior Pituitary Gland Neoplasm", "Recurrent Anterior Pituitary Gland Neoplasm", "Relapsed Neoplasm of the Anterior Pituitary", "Recurrent Tumor of Anterior Pituitary Gland", "Recurrent Neoplasm of the Anterior Pituitary", "Relapsed Neoplasm of Anterior Pituitary Gland", "Relapsed Tumor of the Anterior Pituitary Gland", "Recurrent Neoplasm of Anterior Pituitary Gland", "Recurrent Tumor of the Anterior Pituitary Gland", "Relapsed Neoplasm of the Anterior Pituitary Gland", "Recurrent Neoplasm of the Anterior Pituitary Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Anterior Pituitary Gland Neoplasm", "shortest_name_length": 33}
{"curie": "MONDO:0017825", "names": ["silent pituitary adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "silent pituitary adenoma", "shortest_name_length": 24}
{"curie": "MONDO:0009483", "names": ["Kapur Toriello syndrome", "Kapur-Toriello syndrome", "kapur-Toriello syndrome", "kapur Toriello syndrome", "KAPUR-TORIELLO SYNDROME", "Kapur Toriello syndrome (disorder)", "Kapur Toriello syndrome (diagnosis)", "Cleft lip palate, facial, eye, heart and intestinal anomalies", "cleft lip/palate-facial, eye, heart and intestinal anomalies syndrome", "Cleft lip/palate-facial, eye, heart and intestinal anomalies syndrome", "long columella with cleft lip/palate and eye, heart and intestinal anomalies", "Long columella with cleft lip-palate and eye, heart, and intestinal anomalies", "long columella with cleft Lip/palate and eye, heart, and intestinal anomalies", "LONG COLUMELLA WITH CLEFT LIP/PALATE AND EYE, HEART, AND INTESTINAL ANOMALIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kapur-Toriello syndrome", "shortest_name_length": 23}
{"curie": "UMLS:C4763558", "names": ["Borderline Resectable Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Resectable Malignant Neoplasm", "shortest_name_length": 40}
{"curie": "MONDO:0002164", "names": ["focal chorioretinitis", "Focal chorioretinitis", "focal; chorioretinitis", "chorioretinitis; focal", "focal retinochoroiditis", "Focal retinochoroiditis", "focal; retinochoroiditis", "retinochoroiditis; focal", "Focal chorioretinitis NOS", "Focal chorioretinitis, NOS", "Focal retinochoroiditis NOS", "Focal retinochoroiditis, NOS", "Focal chorioretinitis (disorder)", "Focal chorioretinal inflammation", "focal chorioretinitis (diagnosis)", "Focal chorioretinitis, unspecified", "Focal chorioretinitis and focal retinochoroiditis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal chorioretinitis", "shortest_name_length": 21}
{"curie": "MONDO:0009634", "names": ["Gupta Patton syndrome", "Familial microtia and meatal atresia", "familial microtia and meatal atresia", "Microtia meatal atresia deafness dominant", "microtia meatal atresia deafness dominant", "Microtia, meatal atresia and conductive deafness", "microtia, meatal atresia and conductive deafness", "Microtia with meatal atresia and conductive deafness", "MICROTIA WITH MEATAL ATRESIA AND CONDUCTIVE DEAFNESS", "microtia with meatal atresia and conductive deafness", "familial microtia with meatal atresia and conductive deafness", "Familial microtia with meatal atresia and conductive deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microtia with meatal atresia and conductive deafness", "shortest_name_length": 21}
{"curie": "UMLS:C2698750", "names": ["Pediatric follicular lymphoma", "Pediatric Follicular Lymphoma", "Childhood Follicular Lymphoma", "Paediatric follicular lymphoma", "Pediatric-type follicular lymphoma", "Pediatric-Type Follicular Lymphoma", "Paediatric-type follicular lymphoma", "Pediatric follicular lymphoma (disorder)", "Pediatric follicular lymphoma (diagnosis)", "Pediatric follicular lymphoma (morphologic abnormality)", "malignant neoplasm nodular lymphoma follicular pediatric"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pediatric follicular lymphoma", "shortest_name_length": 29}
{"curie": "MONDO:0011487", "names": ["HDL3", "Huntington disease-like 3", "HUNTINGTON DISEASE-LIKE 3", "Huntington Disease-Like 3", "Huntington disease-like type 3", "HUNTINGTON DISEASE-LIKE 3 (disorder)", "Huntington disease-like 3 (disorder)", "HUNTINGTON DISEASE-LIKE NEURODEGENERATIVE DISORDER, AUTOSOMAL RECESSIVE", "Huntington disease-like neurodegenerative disorder, autosomal recessive", "Huntington Disease-Like Neurodegenerative Disorder, Autosomal Recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Huntington disease-like 3", "shortest_name_length": 4}
{"curie": "MONDO:0011252", "names": ["SEMDSH", "SEMD Shohat type", "SEMD, Shohat type", "SEMD, SHOHAT TYPE", "SEMD, Shohat Type", "spondyloepimetaphyseal dysplasia Shohat type", "Spondyloepimetaphyseal dysplasia Shohat type", "Spondyloepimetaphyseal dysplasia, Shohat type", "spondyloepimetaphyseal dysplasia, Shohat type", "Spondyloepimetaphyseal Dysplasia, Shohat Type", "SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SHOHAT TYPE", "Spondyloepimetaphyseal dysplasia Shohat type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepimetaphyseal dysplasia, Shohat type", "shortest_name_length": 6}
{"curie": "MONDO:0021066", "names": ["renal system tumor", "urinary tract tumor", "Urinary Tract Tumor", "Urinary System Tumor", "urinary system tumor", "renal system neoplasm", "tumor of renal system", "Tumor of Urinary Tract", "tumor of urinary tract", "urinary tract neoplasm", "Urinary Tract Neoplasm", "Tumor of Urinary System", "tumor of urinary system", "Urinary System Neoplasm", "urinary system neoplasm", "neoplasm of renal system", "neoplasm of urinary tract", "Neoplasm of Urinary Tract", "Tumor of the Urinary Tract", "Neoplasm of Urinary System", "neoplasm of urinary system", "tumor of the urinary tract", "Tumor of the Urinary System", "tumor of the urinary system", "Neoplasm of the Urinary Tract", "neoplasm of the urinary tract", "Neoplasm of the Urinary System", "neoplasm of the urinary system", "renal system neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urinary system neoplasm", "shortest_name_length": 18}
{"curie": "MONDO:0009878", "names": ["CPHD2", "Hanhart dwarfism", "Hanhart Dwarfism", "HANHART DWARFISM", "panhypopituitarism", "pituitary dwarfism 3", "PITUITARY DWARFISM III", "Pituitary Dwarfism III", "Pituitary Dwarfism Type 3", "Ateliotic Dwarfism With Hypogonadism", "ateliotic dwarfism with hypogonadism", "ATELIOTIC DWARFISM WITH HYPOGONADISM", "Panhypopituitarism, autosomal recessive", "PITUITARY HORMONE DEFICIENCY, COMBINED, 2", "Pituitary Hormone Deficiency, Combined, 2", "pituitary hormone deficiency, combined, 2", "pituitary hormone deficiency, combined, type 2", "PROP1 combined pituitary hormone deficiencies, genetic form", "combined pituitary hormone deficiencies, genetic form caused by mutation in PROP1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pituitary hormone deficiency, combined, 2", "shortest_name_length": 5}
{"curie": "MONDO:0009476", "names": ["APSB", "jejunum atresia", "Jejunal Atresia", "JEJUNAL ATRESIA", "jejunal atresia", "Jejunal atresia", "atresia; jejunum", "Atresia, Jejunal", "jejunum; atresia", "atresia of jejunum", "Atresia of jejunum", "Atresia of Jejunum", "Jejunoileal atresia", "apple peel syndrome", "apple-peel syndrome", "Apple-peel syndrome", "Imperforate jejunum", "Apple peel syndrome", "APPLE PEEL SYNDROME", "imperforate; jejunum", "jejunum; imperforate", "Small Intestine Atresia", "Small intestine atresia", "small intestine atresia", "Small intestinal atresia", "small intestinal atresia", "Atresia of small intestine", "Atresia of Small Intestine", "atresia of small intestine", "Congenital Jejunal Atresia", "intestinal atresia type IIIb", "anomaly; apple peel syndrome", "Intestinal atresia type IIIb", "apple peel syndrome; anomaly", "Congenital atresia of jejunum", "Congenital Atresia of Jejunum", "apple-peel intestinal atresia", "Hereditary atresia of jejunum", "Atresia of the Small Intestine", "atresia of the small intestine", "Imperforate jejunum (disorder)", "atresia of jejunum (diagnosis)", "Apple Peel Small Bowel Syndrome", "APPLE PEEL SMALL BOWEL SYNDROME", "apple peel small bowel syndrome", "congenital small intestine atresia", "Congenital Small Intestine Atresia", "Congenital small intestinal atresia", "familial apple peel jejunal atresia", "Familial Apple Peel Jejunal Atresia", "Congenital atresia of small intestine", "atresia of small intestine (diagnosis)", "Congenital intestinal atresia syndrome", "Congenital atresia of jejunum (disorder)", "congenital atresia of the small intestine", "Congenital atresia of the small intestine", "Congenital atresia of small intestine (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atresia of small intestine", "shortest_name_length": 4}
{"curie": "UMLS:C0679381", "names": ["Pediatric Disease", "Pediatric Disorder", "disorder pediatric", "pediatric disorder", "pediatric disorders", "disorder pediatrics", "disorders pediatric", "Pediatric Disease or Disorder", "pediatric disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pediatric Disorder", "shortest_name_length": 17}
{"curie": "UMLS:C0340969", "names": ["Pyrimidine-5-nucleotidase deficiency", "Pyrimidine-5'-Nucleotidase Deficiency", "Uridine monophosphate hydrolase deficiency", "Uridine monophosphate hydrolase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uridine monophosphate hydrolase deficiency", "shortest_name_length": 36}
{"curie": "UMLS:C0281594", "names": ["HD during pregnancy", "Hodgkin lymphoma during pregnancy", "Hodgkin Lymphoma During Pregnancy", "Hodgkin's disease during pregnancy", "pregnancy, Hodgkin's disease during"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin Lymphoma During Pregnancy", "shortest_name_length": 19}
{"curie": "MONDO:0007159", "names": ["DA6", "distal arthrogryposis type 6", "Distal arthrogryposis type 6", "arthrogryposis distal type 6", "Arthrogryposis, distal, type 6", "arthrogryposis, distal, type 6", "ARTHROGRYPOSIS, DISTAL, TYPE 6", "Distal arthrogryposis type 6 (disorder)", "arthrogryposis distal type 6 (diagnosis)", "ARTHROGRYPOSIS AND SENSORINEURAL DEAFNESS", "arthrogryposis and sensorineural deafness", "Familial hand abnormality and sensori-neural deafness", "familial hand abnormality and sensori-neural deafness", "Arthrogryposis-like hand anomaly and sensorineural deafness", "arthrogryposis-like hand anomaly and sensorineural deafness", "arthrogryposis-like hand anomaly-sensorineural deafness syndrome", "Arthrogryposis-like hand anomaly-sensorineural deafness syndrome", "Arthrogryposis-like hand anomaly and sensorineural deafness syndrome", "Arthrogryposis-like hand anomaly-sensorineural hearing loss syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis-like hand anomaly-sensorineural deafness syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0017224", "names": ["Pelizaeus-Merzbacher disease in female carriers"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pelizaeus-Merzbacher disease in female carriers", "shortest_name_length": 47}
{"curie": "UMLS:C0744131", "names": ["foot infection fungal", "foot fungal infection", "fungal infection foot", "fungal foot infection", "FOOT INFECTION FUNGAL", "Fungal foot infection", "foot fungal infections", "Foot infection fungal NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fungal foot infection", "shortest_name_length": 21}
{"curie": "UMLS:C0398372", "names": ["Lymph Leakage", "Chyle Leakage", "Lymph leakage", "Escape of lymph", "Leakage of lymph", "Escape of lymph (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymph Leakage", "shortest_name_length": 13}
{"curie": "MONDO:0022612", "names": ["Brunsting-Perry syndrome", "Brunsting Perry syndrome", "Brunsting-Perry pemphigoid", "localized cicatricial pemphigoid", "Brunsting-Perry type cicatricial pemphigoid", "cicatricial pemphigoid of the Brunsting-Perry type", "Brunsting-Perry type cicatricial pemphigoid (disorder)", "Brunsting-Perry type cicatricial pemphigoid (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brunsting-Perry syndrome", "shortest_name_length": 24}
{"curie": "MONDO:0017784", "names": ["EBVaGC", "EBV-Related Gastric Carcinoma", "EBV-associated gastric carcinoma", "EBV-Associated Gastric Carcinoma", "Epstein-Barr Virus-Related Gastric Carcinoma", "Epstein-Barr virus associated gastric carcinoma", "Epstein-Barr Virus-Associated Gastric Carcinoma", "Epstein-Barr virus-associated gastric carcinoma", "Gastric carcinoma due to Epstein-Barr virus disease", "Carcinoma of stomach due to Epstein-Barr virus disease", "Carcinoma of stomach due to Epstein-Barr virus disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epstein-Barr virus-associated gastric carcinoma", "shortest_name_length": 6}
{"curie": "MONDO:0019085", "names": ["VKC", "Spring catarrh", "Vernal Keratoconjunctivitis", "vernal keratoconjunctivitis", "Vernal keratoconjunctivitis", "Keratoconjunctivitis, Vernal", "Vernal Keratoconjunctivitides", "Keratoconjunctivitides, Vernal", "Vernal keratoconjunctivitis (disorder)", "vernal keratoconjunctivitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vernal keratoconjunctivitis", "shortest_name_length": 3}
{"curie": "UMLS:C0242699", "names": ["Bone demineralization", "bone demineralization", "Bone demineralisation", "demineralization; bone", "bones demineralization", "demineralization of bone", "Pathologic Bone Demineralization", "Bone Demineralization, Pathologic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone Demineralization, Pathologic", "shortest_name_length": 21}
{"curie": "UMLS:C0236735", "names": ["Cannabis-Related Disorder", "Cannabis Related Disorder", "Cannabis related disorders", "Cannabis-related disorders", "cannabis-related disorders", "Disorder, Cannabis-Related", "cannabis-related disorders (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cannabis-Related Disorder", "shortest_name_length": 25}
{"curie": "MONDO:0045017", "names": ["cholesterol synthesis disease", "Disorder of cholesterol synthesis", "disorder of cholesterol synthesis", "cholesterol biosynthetic process disease", "disorder of cholesterol biosynthetic process", "Disorder of cholesterol synthesis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholesterol biosynthetic process disease", "shortest_name_length": 29}
{"curie": "MONDO:0001389", "names": ["a.coronaria; anomaly", "coronary artery anomaly", "Coronary artery anomaly", "anomaly coronary artery", "anomaly; coronary artery", "coronary artery; anomaly", "coronary; artery, anomaly", "anomalies artery coronary", "Coronary artery anomalies", "coronary artery abnormality", "Coronary artery abnormality", "abnormalities artery coronary", "Coronary arteries--Abnormalities", "CORONARY ARTERY ANOMALY CONGENITAL", "congenital coronary artery anomaly", "Abnormal coronary artery morphology", "coronary artery anomaly, congenital", "Coronary artery anomaly, congenital", "Congenital anomaly of coronary artery", "congenital anomaly of coronary artery", "coronary artery abnormality [ambiguous]", "Congenital coronary artery malformation", "deformity; artery, coronary, congenital", "artery; deformity, coronary, congenital", "Coronary artery congenital malformation", "Congenital anomaly of coronary artery, NOS", "Congenital coronary artery malformation NOS", "Congenital anomaly of coronary artery (disorder)", "congenital anomaly of coronary artery (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital coronary artery anomaly", "shortest_name_length": 20}
{"curie": "MONDO:0003087", "names": ["Breast Mucoepidermoid Carcinoma", "breast mucoepidermoid carcinoma", "Mucoepidermoid Breast Carcinoma", "mucoepidermoid breast carcinoma", "Mucoepidermoid Carcinoma of Breast", "mucoepidermoid carcinoma of breast", "mucoepidermoid carcinoma of the breast", "Mucoepidermoid Carcinoma of the Breast", "Mucoepidermoid carcinoma of the breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucoepidermoid breast carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0006893", "names": ["Hemorrhagic Septicemia", "hemorrhagic bacteremia", "Hemorrhagic septicemia", "haemorrhagic bacteremia", "hemorrhagic Septicaemia", "bacteremia, hemorrhagic", "Haemorrhagic Septicemia", "Hemorrhagic Septicaemia", "Septicemia, Hemorrhagic", "septicemia, hemorrhagic", "haemorrhagic septicemia", "septicemia, haemorrhagic", "Haemorrhagic Septicaemia", "Septicaemia, hemorrhagic", "bacteremia, haemorrhagic", "haemorrhagic Septicaemia", "Septicaemia, haemorrhagic", "Pasteurella hemorrhagic septicemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pasteurella hemorrhagic septicemia", "shortest_name_length": 22}
{"curie": "UMLS:C4763741", "names": ["Firearm Injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Firearm Injury", "shortest_name_length": 14}
{"curie": "UMLS:C4528553", "names": ["Stage IB Breast Cancer", "Anatomic Stage IB Breast Cancer AJCC v8", "Anatomic Stage IB Breast Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anatomic Stage IB Breast Cancer AJCC v8", "shortest_name_length": 22}
{"curie": "MONDO:0042452", "names": ["tertiary yaws", "Tertiary yaws", "yaws tertiary", "tertiary stage of yaws", "Tertiary stage of yaws", "tertiary lesion of yaws", "Tertiary lesion of yaws", "Tertiary yaws (diagnosis)", "Tertiary lesion of yaws (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tertiary lesion of yaws", "shortest_name_length": 13}
{"curie": "UMLS:C4284020", "names": ["Collapsed Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Collapsed Lung", "shortest_name_length": 14}
{"curie": "UMLS:C0478664", "names": ["adenopathy; localized", "localized; adenopathy", "LYMPHADENOPATHY REGIONAL", "Regional lymphadenopathy", "Localized Lymphadenopathy", "lymphadenopathy; localized", "localized; lymphadenopathy", "gland; hypertrophy, localized", "hypertrophy; gland, localized", "lymph nodes enlarged localized", "lymph node; enlargement, local", "Localized enlarged lymph nodes", "localized enlarged lymph nodes", "enlargement; lymph node, local", "Localised enlarged lymph nodes", "enlargement; lymph node, localized", "lymph node; enlargement, localized", "hypertrophy; lymphatic gland, localized", "lymphatic gland; hypertrophy, localized", "Localized enlarged lymph nodes (disorder)", "localized enlarged lymph nodes (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized enlarged lymph nodes", "shortest_name_length": 21}
{"curie": "MONDO:0009202", "names": ["Thakker-Donnai syndrome", "Thakker Donnai syndrome", "Thakker Donnai syndrome (disorder)", "Dysmorphism multiple structural anomalies", "Facial Dysmorphism with Multiple Malformations", "FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS", "facial dysmorphism with multiple malformations", "Dysmorphism-multiple structural anomalies syndrome", "Facial dysmorphism, multiple structural anomalies syndrome", "Dysmorphic facial features and multiple structural abnormalities", "dysmorphic facial features and multiple structural abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thakker-Donnai syndrome", "shortest_name_length": 23}
{"curie": "UMLS:C1696469", "names": ["shin splint", "Shin Splint", "Shin splints", "splints shin", "Shin Splints", "SHIN SPLINTS", "shin splints", "shin splint injury", "injury shin splints", "shin splint (diagnosis)", "Medial Tibial Stress Syndrome", "Medial tibial stress syndrome", "Medial Tibial Stress Syndromes", "Medial Tibial Stress Syndrome (MTSS)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Medial Tibial Stress Syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0014240", "names": ["PVNH6", "periventricular nodular heterotopia 6", "PERIVENTRICULAR NODULAR HETEROTOPIA 6", "periventricular nodular heterotopia type 6", "ERMARD periventricular nodular heterotopia", "periventricular nodular heterotopia caused by mutation in ERMARD"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "periventricular nodular heterotopia 6", "shortest_name_length": 5}
{"curie": "MONDO:0002443", "names": ["Bruxism", "BRUXISM", "bruxism", "Bruxomania", "grind teeth", "teeth grind", "Sleep Bruxism", "Teeth grating", "TEETH GRATING", "sleep bruxism", "grinding tooth", "Grinding;teeth", "Teeth gnashing", "Grinding tooth", "GRINDING TOOTH", "TEETH-GRINDING", "TEETH GRINDING", "grinding teeth", "tooth grinding", "Grinding teeth", "Teeth-grinding", "Bruxism, Sleep", "Sleep Bruxisms", "teeth grinding", "GNASHING TOOTH", "Teeth Grinding", "Teeth grinding", "Gnashing tooth", "Bruxisms, Sleep", "Nocturnal Bruxism", "Grinding of teeth", "bruxism (disease)", "grinding of teeth", "nocturnal bruxism", "Nocturnal Bruxisms", "Bruxism (disorder)", "Bruxism, Nocturnal", "bruxism (diagnosis)", "Bruxisms, Nocturnal", "grinding one's teeth", "grinding of the teeth", "sleep related bruxism", "Sleep related bruxism", "Sleep-Related Bruxism", "Sleep-related bruxism", "Sleep Related Bruxism", "Bruxism, Sleep-Related", "Sleep-Related Bruxisms", "teeth grinding disorder", "Teeth grinding at night", "Teeth Grinding Disorder", "Bruxisms, Sleep-Related", "Grinding teeth (finding)", "Disorder, Teeth Grinding", "Grinding Disorder, Teeth", "Bruxism - teeth grinding", "bruxism - teeth grinding", "Teeth Grinding Disorders", "grinding teeth disorders", "Teeth grinding while asleep", "Teeth grinding whilst asleep", "grinding one's teeth (symptom)", "Sleep related bruxism (disorder)", "Nocturnal Teeth Grinding Disorder", "Teeth Grinding Disorder, Nocturnal", "Sleep related bruxism (grinding teeth)", "grinding of the teeth (physical finding)", "demonstrated behavior mannerisms grinding teeth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bruxism", "shortest_name_length": 7}
{"curie": "MONDO:0011680", "names": ["ARCI3", "LI5, FORMERLY", "lamellar ichthyosis 5", "ichthyosis, lamellar, 5", "Ichthyosis, Lamellar, 5", "ICHTHYOSIS, LAMELLAR, 5", "Lamellar Ichthyosis, Type 5", "COLLODION BABY, SELF-HEALING", "collodion baby, self-healing", "ichthyosis, lamellar, 5, formerly", "ICHTHYOSIS, LAMELLAR, 5, FORMERLY", "autosomal recessive congenital ichthyosis 3", "ichthyosis, congenital, autosomal recessive 3", "ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 3", "autosomal recessive congenital ichthyosis type 3", "ichthyosis, congenital, autosomal recessive type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive congenital ichthyosis 3", "shortest_name_length": 5}
{"curie": "UMLS:C0153767", "names": ["Stage III Nodular Sclerosis Hodgkin Lymphoma", "Nodular Sclerosis Hodgkin's Disease Stage III", "Stage III Nodular Sclerosis Hodgkin's Disease", "Hodgkin's disease nodular sclerosis stage III", "Nodular Sclerosis Hodgkin's Lymphoma Stage III", "Stage III Nodular Sclerosis Hodgkin's Lymphoma", "Hodgkin lymphoma nodular sclerosis of multiple sites", "nodular sclerosis Hodgkin lymphoma of multiple sites", "Stage III Nodular Sclerosis Classical Hodgkin Lymphoma", "Ann Arbor Stage III Nodular Sclerosis Classic Hodgkin Lymphoma", "Ann Arbor Stage III Nodular Sclerosis Classical Hodgkin Lymphoma", "nodular sclerosis Hodgkin lymphoma of multiple sites (diagnosis)", "Hodgkin's disease, nodular sclerosis, lymph nodes of multiple sites", "Hodgkin disease, nodular sclerosis of lymph nodes of multiple sites", "Hodgkin's disease, nodular sclerosis of lymph nodes of multiple sites", "Hodgkin's disease, nodular sclerosis, involving lymph nodes of multiple sites", "Hodgkin's disease, nodular sclerosis of lymph nodes of multiple sites (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's disease, nodular sclerosis of lymph nodes of multiple sites", "shortest_name_length": 44}
{"curie": "MONDO:0002939", "names": ["Pigmented Basal Cell Carcinoma", "Pigmented basal cell carcinoma", "pigmented basal cell carcinoma", "Carcinoma, Basal Cell, Pigmented", "Skin Pigmented Basal Cell Carcinoma", "skin pigmented basal cell carcinoma", "Pigmented basal cell carcinoma (disorder)", "Pigmented basal cell carcinoma (diagnosis)", "skin neoplasm malignant carcinoma basal cell pigmented", "Pigmented basal cell carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin pigmented basal cell carcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0008871", "names": ["TALS", "MOPD", "Mopd", "MOPD1", "Mopd1", "MopdI", "Mopd I", "MOPD 1", "Mopd 1", "MOPD I", "Taybi-Linder Syndrome", "Taybi-Linder syndrome", "TAYBI-LINDER SYNDROME", "Taybi Linder syndrome", "dwarfism, MOPD type I", "CEPHALOSKELETAL DYSPLASIA", "Cephaloskeletal dysplasia", "cephaloskeletal dysplasia", "brachymelic primordial dwarfism", "BRACHYMELIC PRIMORDIAL DWARFISM", "Brachymelic primordial dwarfism", "dwarfism, MOPD type I (diagnosis)", "osteodysplastic primordial dwarfism type I", "Osteodysplastic Primordial Dwarfism, Type I", "OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I", "Osteodysplastic primordial dwarfism, type 1", "osteodysplastic primordial dwarfism, type 1", "low-birth-weight dwarfism with skeletal dysplasia", "LOW-BIRTH-WEIGHT DWARFISM WITH SKELETAL DYSPLASIA", "Low-birth-weight dwarfism with skeletal dysplasia", "Osteodysplastic primordial dwarfism, type 1 (disorder)", "microcephalic osteodysplastic primordial dwarfism type I", "MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I", "Microcephalic osteodysplastic primordial dwarfism, type 1", "microcephalic osteodysplastic primordial dwarfism, type 1", "Microcephalic Osteodysplastic Primordial Dwarfism, Type I", "microcephalic osteodysplastic primordial dwarfism, type I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephalic osteodysplastic primordial dwarfism type I", "shortest_name_length": 4}
{"curie": "MONDO:0010927", "names": ["OFC3", "OROFACIAL CLEFT 3", "orofacial cleft 3", "Orofacial Cleft 3", "nonsyndromic cleft lip with or without cleft palate 3", "CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 3", "cleft lip with or without cleft palate, nonsyndromic, 3", "Cleft Lip with or without Cleft Palate, Nonsyndromic, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orofacial cleft 3", "shortest_name_length": 4}
{"curie": "MONDO:0005032", "names": ["ADENOMA THYROID", "adenoma thyroid", "THYROID ADENOMA", "thyroid adenoma", "Adenoma thyroid", "Thyroid adenoma", "Thyroid Adenoma", "Adenoma;thyroid", "adenomas thyroid", "Thyroid Adenomas", "Adenoma, Thyroid", "Adenomas, Thyroid", "Adenoma of Thyroid", "adenoma follicular", "follicular adenoma", "ADENOMA FOLLICULAR", "adenoma of thyroid", "Follicular adenoma", "Follicular Adenoma", "Adenoma, Follicular", "Follicular Adenomas", "Thyroid adenoma NOS", "Adenomas, Follicular", "thyroid gland adenoma", "Thyroid Gland Adenoma", "Adenoma of the Thyroid", "adenoma of the thyroid", "Adenoma of Thyroid Gland", "thyroid follicle adenoma", "adenoma of thyroid gland", "thyroid adenoma (disease)", "follicular adenoma thyroid", "thyroid follicular adenoma", "Thyroid Follicular Adenoma", "Thyroid adenoma (disorder)", "Thyroid follicular adenoma", "follicular thyroid adenoma", "THYROID ADENOMA FOLLICULAR", "adenoma follicular thyroid", "THYROID ADENOMA, FOLLICULAR", "Adenoma of the Thyroid Gland", "adenoma of the thyroid gland", "Follicular Adenoma of Thyroid", "follicular adenoma of thyroid", "adenoma, follicular cell, benign", "ADENOMA, FOLLICULAR CELL, BENIGN", "thyroid gland follicular adenoma", "Thyroid Gland Follicular Adenoma", "Follicular Adenoma of the Thyroid", "follicular adenoma of the thyroid", "follicular adenoma of thyroid gland", "Follicular Adenoma of Thyroid Gland", "adenoma of thyroid gland (diagnosis)", "Thyroid follicular adenoma (disorder)", "Follicular Adenoma of the Thyroid Gland", "Follicular adenoma of the Thyroid gland", "follicular adenoma of the thyroid gland", "follicular adenoma (morphologic abnormality)", "Follicular adenoma (morphologic abnormality)", "follicular adenoma of thyroid gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "follicular thyroid adenoma", "shortest_name_length": 15}
{"curie": "MONDO:0009719", "names": ["intracardiac myxoma", "Intracardiac myxoma", "MYXOMA, INTRACARDIAC", "MYXOMA, intracardiac", "Myxoma, Intracardiac", "Familial atrial myxoma", "familial atrial myxoma", "atrial Myxoma, familial", "Atrial myxoma, familial", "ATRIAL MYXOMA, FAMILIAL", "Familial atrial myoxoma", "Familial atrial myxoma (disorder)", "familial atrial myxoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial atrial myxoma", "shortest_name_length": 19}
{"curie": "MONDO:0005080", "names": ["HYPERTENSION PORTAL", "Hypertension;portal", "Hypertension portal", "Portal Hypertension", "portal hypertension", "Portal hypertension", "PORTAL HYPERTENSION", "hypertension portal", "Portal Hypertensions", "Portal hypertensions", "Hypertension, Portal", "hypertension; portal", "HYPERTENSION, PORTAL", "portal; hypertension", "PHT - Portal hypertension", "Portal hypertension syndrome", "Portal hypertension (disorder)", "portal hypertension (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "portal hypertension", "shortest_name_length": 19}
{"curie": "UMLS:C5418920", "names": ["Colon Large Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colon Large Cell Neuroendocrine Carcinoma", "shortest_name_length": 41}
{"curie": "UMLS:C0334395", "names": ["Adenocarcinoma with spindle cell metaplasia", "Adenocarcinoma with Spindle Cell Metaplasia", "adenocarcinoma with spindle cell metaplasia", "adenocarcinoma with spindle cell metaplasia (diagnosis)", "Adenocarcinoma with spindle cell metaplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma with spindle cell metaplasia", "shortest_name_length": 43}
{"curie": "MONDO:0007007", "names": ["Ureaplasma Infection", "ureaplasma infection", "Ureaplasma infection", "Infection, Ureaplasma", "ureaplasma infections", "Ureaplasma urethritis", "Ureaplasma Infections", "Ureaplasma infections", "infection, Ureaplasma", "infections, Ureaplasma", "Infections, Ureaplasma", "Ureaplasma infectious disease", "Ureaplasma disease or disorder", "Ureaplasma urealyticum urethritis", "NGU due to ureaplasma urealyticum", "NGU caused by ureaplasma urealyticum", "Ureaplasma caused disease or disorder", "urethritis due to ureaplasma urealyticum", "ureaplasma urealyticum ('T mycoplasma') urethritis", "urethritis due to ureaplasma urealyticum (diagnosis)", "Nongonococcal urethritis due to Ureaplasma urealyticum", "Nongonococcal urethritis caused by Ureaplasma urealyticum", "Nongonococcal urethritis caused by Ureaplasma urealyticum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ureaplasma urethritis", "shortest_name_length": 20}
{"curie": "MONDO:0016469", "names": ["EDS, vascular-like type", "Ehlers-Danlos syndrome, vascular-like type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ehlers-Danlos syndrome, vascular-like type", "shortest_name_length": 23}
{"curie": "UMLS:C4727399", "names": ["Recurrent Pancreatic Ductal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Pancreatic Ductal Adenocarcinoma", "shortest_name_length": 42}
{"curie": "UMLS:C0281705", "names": ["Stage III Large Cell Lymphoma", "Stage III Pediatric Large Cell Lymphoma", "stage III childhood large cell lymphoma", "Childhood Large Cell Lymphoma Stage III", "Stage III Childhood Large Cell Lymphoma", "Pediatric Large Cell Lymphoma Stage III", "childhood large cell lymphoma, stage III", "stage III large cell lymphoma, childhood", "pediatric large cell lymphoma, stage III", "lymphoma, stage III childhood large cell", "large cell lymphoma, childhood, stage III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Childhood Large Cell Lymphoma", "shortest_name_length": 29}
{"curie": "UMLS:C0012736", "names": ["AORTA ANEURYSM DISSECTING", "DISSECTING AORTIC ANEURYSM", "aortic dissection aneurysm", "Dissecting aortic aneurysm", "Dissecting Aortic Aneurysm", "aneurysm aortic dissecting", "dissecting aortic aneurysm", "dissection aortic aneurysm", "Aortic aneurysm/dissection", "aortic aneurysm dissecting", "aortic aneurysm dissection", "ANEURYSM, AORTA, DISSECTING", "aneurysms aortic dissecting", "Dissecting aortic aneurysms", "dissecting aneurysm of aorta", "aneurysms aortic dissections", "Dissecting aneurysm of aorta", "Aortic aneurysm and dissection", "Aortic aneurysms and dissections", "Dissecting aortic aneurysm (any part)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dissecting aortic aneurysm", "shortest_name_length": 25}
{"curie": "UMLS:C0262929", "names": ["Cardiac Myxoma", "cardiac myxoma", "Cardiac myxoma", "cardiac myxomas", "Endocardial Myxoma", "Endocardium, Myxoma", "ENDOCARDIUM, MYXOMA", "Myxoma of Endocardium", "Myxoma of the Endocardium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myxoma of the Endocardium", "shortest_name_length": 14}
{"curie": "MONDO:0004313", "names": ["Gasserian Meningioma", "Gasserian meningioma", "gasserian ganglion meningioma", "Gasserian ganglion meningioma", "Gasserian Ganglion Meningioma", "meningioma of Gasserian ganglion", "meningioma of Gasserian Ganglion", "Meningioma of Gasserian Ganglion", "meningioma of the Gasserian ganglion", "Meningioma of the Gasserian Ganglion", "gasserian ganglion meningioma (disease)", "meningioma (disease) of gasserian ganglion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gasserian ganglion meningioma", "shortest_name_length": 20}
{"curie": "MONDO:0008773", "names": ["amino aciduria with mental deficiency, dwarfism, muscular dystrophy, osteoporosis and acidosis", "amino aciduria with mental deficiency, dwarfism, muscular dystrophy, osteoporosis, and acidosis", "AMINO ACIDURIA WITH MENTAL DEFICIENCY, DWARFISM, MUSCULAR DYSTROPHY, OSTEOPOROSIS, AND ACIDOSIS", "Amino Aciduria with Mental Deficiency, Dwarfism, Muscular Dystrophy, Osteoporosis, and Acidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amino aciduria with mental deficiency, dwarfism, muscular dystrophy, osteoporosis, and acidosis", "shortest_name_length": 94}
{"curie": "MONDO:0013588", "names": ["PRLTS3", "DFNB81, FORMERLY", "Perrault syndrome 3", "PERRAULT SYNDROME 3", "CLPP Perrault syndrome", "Perrault syndrome type 3", "deafness, autosomal recessive 81", "deafness, autosomal recessive 81, formerly", "DEAFNESS, AUTOSOMAL RECESSIVE 81, FORMERLY", "Perrault syndrome caused by mutation in CLPP"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perrault syndrome 3", "shortest_name_length": 6}
{"curie": "UMLS:C4324497", "names": ["Metastatic Colon Adenocarcinoma", "Adenocarcinoma of colon metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma of colon metastatic", "shortest_name_length": 31}
{"curie": "UMLS:C0472388", "names": ["Cytotoxic Cerebral Edema", "Cytotoxic cerebral edema", "cerebral edema cytotoxic", "Edema, Cytotoxic Cerebral", "Cytotoxic cerebral oedema", "Cerebral Edema, Cytotoxic", "Cytotoxic cerebral edema (disorder)", "cerebral edema cytotoxic (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cytotoxic Cerebral Edema", "shortest_name_length": 24}
{"curie": "MONDO:0013271", "names": ["FND3", "frontonasal dysplasia 3", "FRONTONASAL DYSPLASIA 3", "frontonasal dysplasia type 3", "ALX1-related frontonasal dysplasia", "frontonasal dysplasia - severe microphthalmia - severe facial clefting syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontonasal dysplasia - severe microphthalmia - severe facial clefting syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C2828190", "names": ["Stage IIIB Gestational Trophoblastic Tumor", "Stage IIIB Gestational Trophoblastic Tumor AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Gestational Trophoblastic Tumor AJCC v7", "shortest_name_length": 42}
{"curie": "MONDO:0100062", "names": ["OS", "DEE", "EIEE", "infantile spasm", "Ohtahara Syndrome", "Ohtahara syndrome", "EIEE with Burst-Suppression", "infantile epileptic encephalopathy", "epileptic encephalopathy, infantile", "Early Infantile Epileptic Encephalopathy", "early infantile epileptic encephalopathy", "Early infantile epileptic encephalopathy", "epileptic encephalopathy, early infantile", "developmental and epileptic encephalopathy", "Developmental and Epileptic Encephalopathy", "Early infantile epileptic encephalopathy with burst-suppression", "early infantile epileptic encephalopathy with burst-suppression", "Early Infantile Epileptic Encephalopathy with Burst-Suppression", "early infantile epileptic encephalopathy with suppression-bursts", "Early infantile epileptic encephalopathy with suppression-bursts", "Early infantile epileptic encephalopathy with suppression bursts", "Early infantile epileptic encephalopathy with suppression bursts (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy", "shortest_name_length": 2}
{"curie": "UMLS:C0265050", "names": ["v.cava; thrombosis", "VENA CAVA THROMBOSIS", "vena cava thrombosis", "Vena cava thrombosis", "cava thrombosis vena", "Vena Cava Thrombosis", "Vena caval thrombosis", "thrombosis; vena cava", "thrombosis of vena cava", "Thrombosis of vena cava", "Thrombosis of vena cava (disorder)", "thrombosis of vena cava (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thrombosis of vena cava", "shortest_name_length": 18}
{"curie": "MONDO:0018129", "names": ["Autosomal recessive cerebellar ataxia due to GBA2 deficiency", "autosomal recessive cerebellar ataxia due to GBA2 deficiency", "Autosomal recessive cerebellar ataxia with late-onset spasticity", "autosomal recessive cerebellar ataxia with late-onset spasticity", "Autosomal recessive cerebellar ataxia with late-onset spasticity (disorder)", "Autosomal recessive cerebellar ataxia due to GBA2 (glucosylceramidase beta 2) deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive cerebellar ataxia with late-onset spasticity", "shortest_name_length": 60}
{"curie": "MONDO:0008318", "names": ["Proteus syndrome", "proteus syndrome", "Proteus Syndrome", "PROTEUS SYNDROME", "proteiform syndrome", "Elephant Man Disease", "Wiedemann's syndrome", "disease elephant man", "elephant man disease", "Wiedemann syndrome 2", "Proteus syndrome (PS)", "disease elephant mans", "Elattoproteus syndrome", "ELATTOPROTEUS SYNDROME", "diseases elephant mans", "proteus syndrome, somatic", "Proteus syndrome (disorder)", "hemihypertrophy and macrocephaly", "Hemihypertrophy and macrocephaly", "Macrocephaly mesodermal hamartoma spectrum", "partial gigantism-nevi-hemihypertrophy-macrocephaly syndrome", "Partial gigantism-nevi-hemihypertrophy-macrocephaly syndrome", "Partial gigantism of hands and feet, nevi, hemihypertrophy, macrocephaly", "partial gigantism of hands and feet, nevi, hemihypertrophy, macrocephaly", "Gigantism, partial, of hands and feet, nevi, hemihypertrophy, and macrocephaly", "GIGANTISM, PARTIAL, OF HANDS AND FEET, NEVI, HEMIHYPERTROPHY, AND MACROCEPHALY", "gigantism, partial, of hands and feet, nevi, hemihypertrophy, and macrocephaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Proteus syndrome", "shortest_name_length": 16}
{"curie": "UMLS:C0030631", "names": ["Passive-aggressive personality", "Passive-Aggressive Personality", "aggressive passive personality", "Passive Aggressive Personality", "passive aggressive personality", "passive-aggressive personality", "Personality, Passive-Aggressive", "Passive-Aggressive Personalities", "Negativistic Personality Disorder", "Personalities, Passive-Aggressive", "Personality Disorder, Negativistic", "negativistic; personality disorder", "Disorder, Negativistic Personality", "personality disorder; negativistic", "Negativistic Personality Disorders", "Disorders, Negativistic Personality", "Personality Disorders, Negativistic", "Passive aggressive personality disorder", "passive aggressive personality disorder", "Passive-Aggressive Personality Disorder", "Passive Aggressive Personality Disorder", "Passive-aggressive personality disorder", "Passive-Aggressive Personality Disorders", "passive-aggressive; personality disorder", "Passive Aggressive Personality Disorders", "Personality Disorder, Passive-Aggressive", "Disorder, Passive-Aggressive Personality", "Personality Disorder, Passive Aggressive", "personality disorder; passive-aggressive", "Personality Disorders, Passive-Aggressive", "Disorders, Passive-Aggressive Personality", "Personality Disorders, Passive Aggressive", "Passive aggressive personality disorder (disorder)", "passive aggressive personality disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Passive-Aggressive Personality Disorder", "shortest_name_length": 30}
{"curie": "UMLS:C5238796", "names": ["Ox/Phos", "Muscular Dystrophy Secondary to Oxidative Phosphorylation Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Muscular Dystrophy Secondary to Oxidative Phosphorylation Disorder", "shortest_name_length": 7}
{"curie": "MONDO:0014351", "names": ["PCH9", "Pontocerebellar hypoplasia type 9", "pontocerebellar hypoplasia type 9", "PONTOCEREBELLAR HYPOPLASIA, TYPE 9", "pontocerebellar hypoplasia, type 9", "AMPD2 non-syndromic pontocerebellar hypoplasia", "non-syndromic pontocerebellar hypoplasia caused by mutation in AMPD2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pontocerebellar hypoplasia type 9", "shortest_name_length": 4}
{"curie": "MONDO:0013009", "names": ["Megarbane-Jalkh Syndrome", "Megarbane Jalkh Syndrome", "Megarbane Jalkh syndrome", "Megarbane-Jalkh syndrome", "MEGARBANE-JALKH SYNDROME", "developmental delay dysmorphic features neonatal spontaneous fractures wrinkled skin and hepatic failure", "developmental delay, dysmorphic features, neonatal spontaneous fractures, wrinkled skin, and hepatic failure", "Developmental Delay, Dysmorphic Features, Neonatal Spontaneous Fractures, Wrinkled Skin, And Hepatic Failure", "DEVELOPMENTAL DELAY, DYSMORPHIC FACIAL FEATURES, NEONATAL SPONTANEOUS FRACTURES, WRINKLED SKIN, AND HEPATIC FAILURE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Megarbane-Jalkh syndrome", "shortest_name_length": 24}
{"curie": "MONDO:0006980", "names": ["Struma Ovarii", "STRUMA OVARII", "struma ovarii", "Struma ovarii", "struma; ovarii", "Struma ovarii NOS", "Struma ovarii, NOS", "ovary tumor thyroid", "OVARY, THYROID TUMOR", "OVARIAN CANCER, STRUMA OVARII", "benign struma ovarii of ovary", "Struma ovarii (morphologic abnormality)", "struma ovarii (morphologic abnormality)", "benign struma ovarii of ovary (diagnosis)", "struma ovarii NOS (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "struma ovarii", "shortest_name_length": 13}
{"curie": "UMLS:C0853762", "names": ["Hot flushes aggravated", "Aggravation of hot flushes", "Exacerbation of hot flushes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aggravation of hot flushes", "shortest_name_length": 22}
{"curie": "UMLS:C0152008", "names": ["Vulvovaginal disease", "VULVOVAGINAL DISORDER", "Disorder vulvovaginal", "DISORDER VULVOVAGINAL", "Vulvovaginal disorder", "Vulvovaginal disease, NOS", "Vulvovaginal disorder NOS", "Vulvovaginal disorder, NOS", "Vulvovaginal disease (disorder)", "Disease or syndrome of vagina and vulva"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvovaginal disease", "shortest_name_length": 20}
{"curie": "MONDO:0043243", "names": ["leukoplakia", "Leukoplakia", "LEUKOPLAKIA", "Leucoplakia", "leucoplakia", "leukoplakias", "Leukoplakias", "leukokeratoses", "leukokeratosis", "Leukoplakia NOS", "Keratotic Plaque", "Leukoplakia, NOS", "keratotic plaque", "Leukoplakic Lesion", "leukoplakic lesion", "Leukoplakic Lesions", "leukoplakic lesions", "Lesion, Leukoplakic", "lesion, leukoplakic", "lesions, leukoplakic", "Lesions, Leukoplakic", "Leukoplakia (disorder)", "Leukoplakia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukoplakia", "shortest_name_length": 11}
{"curie": "MONDO:0002781", "names": ["IXth nerve paralysis", "Cranial nerve palsy IX", "Cranial Nerve IX Palsy", "Ninth cranial nerve palsy", "Ninth Cranial Nerve Palsy", "n.glossopharyngeus; paralysis", "Palsy of glossopharyngeal nerve", "glossopharyngeal nerve paralysis", "Glossopharyngeal Nerve Paralysis", "Glossopharyngeal nerve paralysis", "Palsy of glossopharyngeal nerve (disorder)", "glossopharyngeal nerve cranial nerve palsy", "cranial nerve palsy of glossopharyngeal nerve"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glossopharyngeal nerve paralysis", "shortest_name_length": 20}
{"curie": "UMLS:C0152973", "names": ["serratia sepsis", "Serratia sepsis", "Serratia septicemia", "Septicemia serratia", "Septicaemia serratia", "Serratia septicaemia", "Septicemia due to serratia", "Septicemia due to Serratia", "Septicaemia due to serratia", "Septicaemia due to Serratia", "Serratia septicemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Serratia sepsis", "shortest_name_length": 15}
{"curie": "UMLS:C1335028", "names": ["Non-Neoplastic Parathyroid Gland Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Parathyroid Gland Disorder", "shortest_name_length": 41}
{"curie": "MONDO:0021326", "names": ["cervical part of esophagus cancer", "cancer of cervical part of esophagus", "malignant tumor of cervical esophagus", "Malignant Neoplasm of Cervical Esophagus", "Malignant neoplasm of cervical esophagus", "malignant neoplasm of cervical esophagus", "Malignant neoplasm of cervical oesophagus", "malignant neoplasm of the cervical esophagus", "Malignant Neoplasm of the Cervical Esophagus", "Malignant tumor of cervical part of esophagus", "malignant cervical part of esophagus neoplasm", "Malignant tumour of cervical part of oesophagus", "Malignant neoplasm of cervical part of esophagus", "malignant neoplasm of cervical part of esophagus", "Malignant neoplasm of cervical part of oesophagus", "malignant neoplasm of cervical esophagus (diagnosis)", "Malignant tumor of cervical part of esophagus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant neoplasm of cervical esophagus", "shortest_name_length": 33}
{"curie": "UMLS:C0863090", "names": ["Allergic skin reaction", "skin allergic reaction", "allergic skin reaction", "allergic reaction skin", "allergic reactions skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Allergic skin reaction", "shortest_name_length": 22}
{"curie": "UMLS:C0023420", "names": ["Leukemia L1210", "Leukemia L 1210", "L1210, Leukemia", "L 1210, Leukemia", "mouse leukemia L1210"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leukemia L1210", "shortest_name_length": 14}
{"curie": "MONDO:0002978", "names": ["Orbit Alveolar Rhabdomyosarcoma", "orbit rhabdomyosarcoma alveolar", "orbit alveolar rhabdomyosarcoma", "alveolar rhabdomyosarcoma of orbit", "Alveolar Rhabdomyosarcoma of Orbit", "Alveolar Rhabdomyosarcoma of the orbit", "alveolar rhabdomyosarcoma of the orbit", "Alveolar Rhabdomyosarcoma of the Orbit", "alveolar rhabdomyosarcoma of orbit (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orbit alveolar rhabdomyosarcoma", "shortest_name_length": 31}
{"curie": "UMLS:C4525746", "names": ["Stage IIB Colon Neuroendocrine Tumor", "Stage IIB Colon Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Colon Neuroendocrine Tumor AJCC v8", "shortest_name_length": 36}
{"curie": "MONDO:0000467", "names": ["Partial AV block", "AV block, partial", "Partial heart block", "AV block, incomplete", "AV block second degree", "second degree av block", "AV BLOCK SECOND DEGREE", "second degree AV block", "av block degree second", "Second degree AV block", "2nd degree heart block", "Second Degree AV Block", "Incomplete heart block", "AV Block Second Degree", "second degree A-V block", "A-V block second degree", "Second Degree Heart Block", "HEART BLOCK SECOND DEGREE", "second degree heart block", "Second-degree heart block", "second-degree heart block", "Heart block second degree", "Second degree heart block", "HEART BLOCK AV SECOND DEGREE", "Heart block AV second degree", "Partial atrioventricular block", "Atrioventricular block, partial", "Incomplete atrioventricular block", "Atrioventricular block incomplete", "Atrioventricular block, incomplete", "Second-degree atrioventricular block", "Second Degree Atrioventricular Block", "Second degree atrioventricular block", "second-degree atrioventricular block", "Atrioventricular block second degree", "Atrioventricular Block Second Degree", "atrioventricular block second degree", "second degree atrioventricular block", "Atrioventricular Block, Second Degree", "Atrioventricular block, second degree", "atrioventricular block, second degree", "Partial atrioventricular block (disorder)", "Second degree atrioventricular heart block", "block; heart, second degree (atrioventricular)", "heart; block, second degree (atrioventricular)", "Second degree atrioventricular block (disorder)", "Incomplete atrioventricular block, second degree", "second degree atrioventricular block (diagnosis)", "Incomplete atrioventricular block, second degree NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "second-degree atrioventricular block", "shortest_name_length": 16}
{"curie": "UMLS:C4054694", "names": ["Ivory Exostosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ivory Exostosis", "shortest_name_length": 15}
{"curie": "MONDO:0001461", "names": ["body tinea", "Body tinea", "tinea body", "body ringworm", "Tinea corporis", "TINEA CORPORIS", "corporis tinea", "Tinea Corporis", "tinea corporis", "ringworm; body", "body; ringworm", "tinea; corporis", "TINEA CIRCINATA", "corporis; tinea", "Tinea circinata", "Tinea circinatus", "of body ringworm", "Ringworm of body", "herpes circinatus", "Herpes circinatus", "herpes; circinatus", "circinatus; herpes", "Ringworm of the body", "DERMATOPHYTOSIS BODY", "dermatophytosis; body", "body; dermatophytosis", "Dermatophytosis of body", "Tinea corporis (disorder)", "tinea corporis (diagnosis)", "dermatophytosis of the body", "Dermatophytosis of the body", "dermatophytosis of the trunk", "Dermatophytosis of the trunk"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tinea corporis", "shortest_name_length": 10}
{"curie": "MONDO:0001762", "names": ["dentine erosion", "Erosion, extending into dentine", "dentine tooth erosion, non-bacterial", "tooth erosion, non-bacterial of dentine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dentine erosion", "shortest_name_length": 15}
{"curie": "MONDO:0017199", "names": ["Heide syndrome", "osteoporosis-macrocephaly-blindness-joint hyperlaxity syndrome", "Osteoporosis-macrocephaly-blindness-joint hyperlaxity syndrome", "Osteoporosis and macrocephaly with blindness and joint hyperlaxity syndrome", "Osteoporosis and macrocephaly with blindness and joint hypermobility syndrome", "Osteoporosis and macrocephaly with blindness and joint hypermobility syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteoporosis-macrocephaly-blindness-joint hyperlaxity syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C4744712", "names": ["Advanced Prostate Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Prostate Carcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C4331026", "names": ["Posterior Fossa Ependymal Tumor", "Posterior Cranial Fossa Ependymal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Posterior Fossa Ependymal Tumor", "shortest_name_length": 31}
{"curie": "UMLS:C4682655", "names": ["Gestational Trophoblastic Neoplasm by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gestational Trophoblastic Neoplasm by AJCC v8 Stage", "shortest_name_length": 51}
{"curie": "MONDO:0013049", "names": ["DG1O", "CDGIo", "CDG1o", "CDG1O", "CDG-Io", "CDG Io", "MDDGC15", "DPM3-CDG", "CDG1(DPM3)", "Cdg1(Dpm3)", "DPM3-CDG (CDG-Io)", "CDG syndrome type Io", "DPM3-congenital disorder of glycosylation", "congenital disorder of glycosylation type 1o", "Congenital disorder of glycosylation type 1o", "congenital disorder of glycosylation type Io", "Congenital disorder of glycosylation type Io", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Io", "congenital disorder of glycosylation, type Io", "Congenital Disorder of Glycosylation, Type Io", "carbohydrate deficient glycoprotein syndrome type Io", "Carbohydrate deficient glycoprotein syndrome type 1o", "Carbohydrate deficient glycoprotein syndrome type Io", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 15", "Carbohydrate deficient glycoprotein syndrome type 1o (disorder)", "muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 15", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, DPM3-RELATED", "DPM3-CDG - dolichyl-phosphate mannosyltransferase 3 congenital disorder of glycosylation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DPM3-congenital disorder of glycosylation", "shortest_name_length": 4}
{"curie": "UMLS:C4682862", "names": ["Tumor Stage (Pathological)", "Renal Cell Cancer by AJCC v8 Stage", "Renal Cell Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal Cell Cancer by AJCC v8 Stage", "shortest_name_length": 26}
{"curie": "UMLS:C4521717", "names": ["Stage III Esophageal Adenocarcinoma", "Postneoadjuvant Therapy Stage III Esophageal Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postneoadjuvant Therapy Stage III Esophageal Adenocarcinoma AJCC v8", "shortest_name_length": 35}
{"curie": "MONDO:0020709", "names": ["Majocchi granuloma", "Majocchi's granuloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Majocchi granuloma", "shortest_name_length": 18}
{"curie": "MONDO:0009720", "names": ["KPTS", "KEIPERT SYNDROME", "Keipert Syndrome", "Keipert syndrome", "Nasodigitoacoustic syndrome", "Keipert syndrome (disorder)", "nasodigitoacoustic syndrome", "Keipert syndrome, X-linked recessive", "NASODIGITOACOUSTIC SYNDROME, FORMERLY", "nasodigitoacoustic syndrome, formerly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Keipert syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0017795", "names": ["aot", "adamantinoma", "Adamantinoma", "ADAMANTINOMA", "AMELOBLASTOMA", "Ameloblastoma", "ameloblastoma", "Ameloblastomas", "adamantinoma; jaw", "jaw; adamantinoma", "Ameloblastoma NOS", "Adenoameloblastoma", "Ameloblastoma, NOS", "jaw; ameloblastoma", "ameloblastoma; jaw", "Adamantinoma of jaw", "ameloblastoma of jaw", "Ameloblastoma of jaw", "EPITHELIOMA ADAMANTINUM", "adenomatoid odontogenic tumor", "Ameloblastoma of jaw (disorder)", "Ameloblastoma (morphologic abnormality)", "Adamantinoma (except of Tibia and Long bones, M-92613)", "Adamantinoma, NOS (except of Tibia and Long bones, M-92613)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ameloblastoma", "shortest_name_length": 3}
{"curie": "UMLS:C0860155", "names": ["mi non q wave", "non-q wave mi", "non q wave mi", "Non-Q wave MI", "mi non-q wave"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Q wave MI", "shortest_name_length": 13}
{"curie": "MONDO:0017808", "names": ["DPG-plus syndrome", "hypophyseal duplication", "duplication of the pituitary gland", "Duplication of the pituitary gland-plus syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "duplication of the pituitary gland", "shortest_name_length": 17}
{"curie": "MONDO:0005044", "names": ["HTN", "HBP", "htn", "hbp", "high bp", "BP raised", "Raised BP", "Rise in BP", "elevated bp", "hyperpiesis", "Hyperpiesis", "Elevated BP", "Hyperpiesia", "hyperpiesia", "HYPERTENSION", "hypertension", "Hypertension", "Increased BP", "systemic HTN", "Hypertension NOS", "Hypertension, NOS", "HT - Hypertension", "HTN - Hypertension", "BP+ - Hypertension", "BLOOD PRESSURE HIGH", "High Blood Pressure", "high blood pressure", "blood high pressure", "blood pressure rise", "Blood pressure high", "High blood pressure", "blood pressure, high", "HYPERTENSIVE DISEASE", "blood pressure; high", "Hypertensive disease", "blood pressure rises", "pressure, high blood", "Blood Pressure, High", "hypertensive disease", "high; blood pressure", "High Blood Pressures", "raised blood pressure", "vascular hypertension", "Hypertensive disorder", "Blood pressure raised", "Blood Pressures, High", "Raised blood pressure", "hypertensive disorder", "systemic hypertension", "HYPERTENSIVE DISEASES", "arterial hypertension", "Hypertensive diseases", "Hypertension arterial", "Systemic hypertension", "HYPERTENSION ARTERIAL", "Arterial hypertension", "blood pressure raising", "elevate blood pressure", "Hypertension, arterial", "Arterial pressure high", "high; arterial tension", "rise in blood pressure", "ARTERIAL PRESSURE HIGH", "blood elevate pressure", "Rise in blood pressure", "increase blood pressure", "elevated blood pressure", "Elevated blood pressure", "blood increase pressure", "blood pressure increase", "blood pressure elevated", "blood elevates pressure", "BLOOD PRESSURE ELEVATED", "Elevated Blood Pressure", "Pressure blood increased", "Blood pressure increased", "blood elevation pressure", "BP - High blood pressure", "elevation blood pressure", "blood pressure elevation", "Increased blood pressure", "increased blood pressure", "PRESSURE BLOOD INCREASED", "blood increases pressure", "Blood pressure elevation", "BLOOD PRESSURE INCREASED", "BLOOD PRESSURE ELEVATION", "blood elevations pressure", "blood pressure, increased", "increased; blood pressure", "blood pressure; increased", "Hypertensive disease, NOS", "HBP - High blood pressure", "blood increasing pressure", "increase in blood pressure", "Increase in blood pressure", "Pressure arterial increased", "High blood pressure disorder", "high blood pressure disorder", "Hypertensive vascular disease", "hypertensive vascular disease", "Systemic arterial hypertension", "Vascular Hypertensive Disorder", "arterial hypertension systemic", "systemic arterial hypertension", "vascular hypertensive disorder", "Arterial pressure NOS increased", "Vascular hypertensive disorders", "Elevated BP (excluding K86 K87)", "High Blood Pressure/ Hypertension", "systemic hypertension (diagnosis)", "Hypertension (high blood pressure)", "Hypertensive vascular degeneration", "Finding of increased blood pressure", "Hypertensive disorder, systemic arterial", "Finding of increased blood pressure (finding)", "Hypertensive cardiovascular disease or syndrome", "Hypertensive disorder, systemic arterial (disorder)", "Complications affecting other specified body systems, not elsewhere classified, hypertension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertensive disorder", "shortest_name_length": 3}
{"curie": "MONDO:0005156", "names": ["Myeloencephalitis", "Encephalomyelitis", "ENCEPHALOMYELITIS", "myeloencephalitis", "encephalomyelitis", "Myeloencephalitides", "Encephalomyelitis, NOS", "encephalitis &/or myelitis", "Encephalitis &/or myelitis", "Encephalomyelitis (disorder)", "encephalitis and/or myelitis", "encephalomyelitis (diagnosis)", "Inflammation of brain and spine", "central nervous system inflammation", "inflammation of central nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephalomyelitis", "shortest_name_length": 17}
{"curie": "MONDO:0012969", "names": ["MVCD5", "retinopathy, diabetic, susceptibility to", "microvascular complications of diabetes 5", "PON1 microvascular complications of diabetes, susceptibility", "microvascular complications of diabetes, susceptibility to, 5", "microvascular complications of diabetes, susceptibility to, type 5", "microvascular complications of diabetes, susceptibility caused by mutation in PON1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microvascular complications of diabetes, susceptibility to, 5", "shortest_name_length": 5}
{"curie": "MONDO:0019355", "names": ["AOSD", "Still; adult-onset", "adult-onset; Still", "adult still disease", "adult disease still", "STILL DISEASE ADULT", "adult disease stills", "still's adult disease", "adults disease stills", "ADULT STILL'S DISEASE", "adult Still's disease", "adult still's disease", "Adult Still's Disease", "Wissler-Fanconi syndrome", "adult-onset Still disease", "Adult-onset Still disease", "Adult onset Still disease", "Adult-Onset Still Disease", "Adult Onset Still Disease", "Adult-Onset Stills Disease", "Still Disease, Adult Onset", "adult-onset stills disease", "adult disease onset stills", "Still Disease, Adult-Onset", "adult-onset Still's disease", "Stills Disease, Adult-Onset", "Adult-Onset Still's Disease", "adult-onset still's disease", "Still's disease adult onset", "Adult Onset Still's Disease", "Adult onset Still's disease", "Adult-onset Still's disease", "adult onset still's disease", "adult onset Still's disease", "Still's Disease, Adult Onset", "Still's Disease, Adult-Onset", "Still's adult onset; disease", "disease; Still's adult onset", "AOSD (adult onset Still's disease)", "Adult onset Still's disease (disorder)", "adult onset Still's disease (diagnosis)", "Adult-onset Still's disease, site unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult-onset Still disease", "shortest_name_length": 4}
{"curie": "MONDO:0019649", "names": ["idiopathic steroid-sensitive nephrotic syndrome with focal segmental hyalinosis", "idiopathic steroid-sensitive nephrotic syndrome with focal segmental glomerulosclerosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic steroid-sensitive nephrotic syndrome with focal segmental hyalinosis", "shortest_name_length": 79}
{"curie": "MONDO:0005463", "names": ["AORTIC VALVE CALCIFIC", "Calcified aortic valve", "calcified aortic valve", "calcific aortic stenosis", "Aortic Stenosis, Calcific", "AORTIC STENOSIS, CALCIFIC", "aortic calcification valve", "aortic valve calcification", "Aortic valve calcification", "Aortic valve calcifications", "Calcification of aortic valve", "AORTIC VALVE, CALCIFICATION OF", "Aortic Valve, Calcification of", "aortic valve calcification (disease)", "calcific aortic stenosis (diagnosis)", "Aortic valve calcification (disorder)", "aortic valve calcification (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic valve calcification", "shortest_name_length": 21}
{"curie": "UMLS:C4284917", "names": ["HSDB", "Adrenal Gland Hyperplasia II", "3-Beta-Hydroxysteroid Dehydrogenase Deficiency", "Adrenal Gland Hyperplasia, Congenital, due to 3-Beta-Hydroxysteroid Dehydrogenase 2 Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adrenal Gland Hyperplasia II", "shortest_name_length": 4}
{"curie": "MONDO:0007246", "names": ["CALCIFIC AORTIC DISEASE WITH IMMUNOLOGIC ABNORMALITIES, FAMILIAL", "calcific aortic disease with immunologic abnormalities, familial", "Calcific Aortic Disease with Immunologic Abnormalities, Familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "calcific aortic disease with immunologic abnormalities, familial", "shortest_name_length": 64}
{"curie": "UMLS:C0969676", "names": ["Uniparental isodisomy", "Uniparental Isodisomy", "Uniparental Isodisomies", "Isodisomies, Uniparental"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uniparental Isodisomy", "shortest_name_length": 21}
{"curie": "MONDO:0014039", "names": ["MTDPS11", "PEO-myopathy-emaciation syndrome", "mitochondrial DNA depletion syndrome 11", "MITOCHONDRIAL DNA DEPLETION SYNDROME 11", "MGME1 mitochondrial DNA depletion syndrome", "mitochondrial DNA depletion syndrome type 11", "mtDNA maintenance syndrome due to MGME1 deficiency", "mitochondrial DNA maintenance syndrome due to MGME1 deficiency", "mitochondrial DNA depletion syndrome caused by mutation in MGME1", "progressive external ophthalmoplegia-myopathy-emaciation syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial DNA depletion syndrome 11", "shortest_name_length": 7}
{"curie": "UMLS:C0149622", "names": ["flaccid bladder", "BLADDER, FLACCID", "BLADDER, PARALYTIC", "motor paralytic bladder", "BLADDER, MOTOR PARALYTIC", "atonic neurogenic bladder", "ATONIC NEUROGENIC BLADDER", "Atonic Neurogenic Bladder", "Neurogenic Bladder, Atonic", "BLADDER, NEUROGENIC ATONIC", "Atonic bladder (neurogenic)", "Neurogenic Urinary Bladder, Atonic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neurogenic Urinary Bladder, Atonic", "shortest_name_length": 15}
{"curie": "MONDO:0009131", "names": ["FD", "DYS", "HSN 3", "HSAN3", "HSAN 3", "HSN-III", "HSAN III", "Riley-Day", "Riley- Day", "HSAN Type III", "Riley Day syndrome", "Riley-Day syndrome", "Riley-Day Syndrome", "RILEY-DAY SYNDROME", "Riley Day Syndrome", "riley-day syndrome", "riley day syndrome", "riley days syndrome", "dysautonomia familial", "Familial Dysautonomia", "familial dysautonomia", "Familial dysautonomia", "dysautonomia, familial", "Dysautonomia, Familial", "DYSAUTONOMIA, FAMILIAL", "Familial dysautonomia (disorder)", "familial dysautonomia (diagnosis)", "Familial dysautonomia [Riley-Day]", "hereditary sensory neuropathy type 3", "Hereditary Sensory Neuropathy Type 3", "familial autonomic nervous dysfunction", "familial dysautonomia (Riley-Day syndrome)", "Hereditary Sensory and Autonomic Neuropathy 3", "hereditary sensory and autonomic neuropathy 3", "Type 3 Hereditary Sensory Neuropathy, Dominant", "Neuropathy, Hereditary and Autonomic, Type III", "Hereditary sensory neuropathy, type 3, dominant", "Hereditary Sensory Neuropathy, Type 3, Dominant", "Hereditary Sensory Neuropathy, Dominant, Type 3", "Dominant Hereditary Sensory Neuropathy, Type III", "Type III Hereditary Sensory Neuropathy, Dominant", "Dominant hereditary sensory neuropathy, type III", "Hereditary Sensory Neuropathy, Dominant, Type III", "Hereditary sensory and autonomic neuropathy type 3", "hereditary sensory and autonomic neuropathy type 3", "hereditary sensory and autonomic neuropathy type III", "Hereditary-Sensory and Autonomic Neuropathy Type III", "neuropathy, hereditary sensory and autonomic, type 3", "Hereditary Sensory and Autonomic Neuropathy Type III", "Hereditary sensory and autonomic neuropathy type III", "Hereditary sensory and autonomic neuropathy, type III", "Neuropathy, Hereditary Sensory And Autonomic, Type III", "Neuropathy, Hereditary Sensory and Autonomic, Type III", "NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III", "neuropathy, hereditary sensory and autonomic, type III", "HSAN (Hereditary Sensory and Autonomic Neuropathy) Type III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Riley-Day syndrome", "shortest_name_length": 2}
{"curie": "MONDO:0007285", "names": ["CZP", "CZP1", "CAE1", "CTRCT1", "Duffy linked cataract", "CATARACT, DUFFY-LINKED", "cataract, Duffy-linked", "Cataract, Duffy-Linked", "GJA8 cataract (disease)", "cataract 1 multiple types", "CATARACT 1, MULTIPLE TYPES", "cataract 1, multiple types", "Pulverulent Zonular Cataract", "Cataract, zonular pulverulent", "zonular pulverulent cataract 1", "CATARACT 1, ZONULAR PULVERULENT", "Cataract, Zonular Pulverulent 1", "CATARACT, ZONULAR PULVERULENT, 1", "cataract, zonular pulverulent, 1", "cataract (disease) caused by mutation in GJA8", "cataract 1, multiple types, with or without microcornea", "CATARACT 1, MULTIPLE TYPES, WITH OR WITHOUT MICROCORNEA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 1 multiple types", "shortest_name_length": 3}
{"curie": "MONDO:0019457", "names": ["secondary AML", "Secondary AGL", "Secondary AML", "SECONDARY_AML", "secondary ANLL", "Therapy-Related AML and MDS", "Alkylating Agent-Related AML", "Secondary Acute Myeloid Leukemia", "secondary acute myeloid leukemia", "Therapy-Related Myeloid Neoplasm", "Secondary acute myeloid leukemia", "acute myeloid leukemia, secondary", "myeloid leukemia, secondary acute", "Secondary Acute Myelocytic Leukemia", "Secondary Acute myelocytic Leukemia", "Secondary Acute Myelogenous Leukemia", "Secondary Acute myelogenous Leukemia", "secondary acute myelogenous leukemia", "Secondary Acute Myeloblastic Leukemia", "acute myelogenous leukemia, secondary", "myelogenous leukemia, secondary acute", "Secondary Acute myeloblastic Leukemia", "Secondary Acute granulocytic Leukemia", "Secondary Acute Granulocytic Leukemia", "Secondary Acute myeloid Leukemia (AML)", "Secondary Acute Myeloid Leukemia (AML)", "secondary acute nonlymphocytic leukemia", "secondary acute non-lymphocytic leukemia", "acute nonlymphocytic leukemia, secondary", "nonlymphocytic leukemia, secondary acute", "acute non-lymphocytic leukemia, secondary", "non-lymphocytic leukemia, secondary acute", "secondary acute nonlymphoblastic leukemia", "acute nonlymphoblastic leukemia, secondary", "secondary acute non-lymphoblastic leukemia", "nonlymphoblastic leukemia, secondary acute", "acute non-lymphoblastic leukemia, secondary", "non-lymphoblastic leukemia, secondary acute", "Alkylating Agent-Related Acute Myeloid Leukemia", "Alkylating Agent Related Acute Myeloid Leukemia", "Therapy-related AML and myelodysplastic syndrome", "therapy-related AML and myelodysplastic syndrome", "Therapy-related acute myeloid leukemia, alkylating agent related", "Therapy-related acute myeloid leukaemia, alkylating agent related", "Therapy-related acute myeloid leukemia, epipodophyllotoxin-related", "Therapy-related acute myeloid leukemia and myelodysplastic syndrome", "Therapy related acute myeloid leukemia and myelodysplastic syndrome", "therapy related acute myeloid leukemia and myelodysplastic syndrome", "Therapy-related acute myeloid leukaemia, epipodophyllotoxin-related", "acute therapy related myeloid leukemia and myelodysplastic syndrome", "Therapy-Related Acute Myeloid Leukemia and Myelodysplastic Syndrome", "Therapy-related acute myeloid leukaemia and myelodysplastic syndrome", "Therapy related acute myeloid leukaemia and myelodysplastic syndrome", "Acute Myeloid Leukaemias and Myelodysplastic Syndromes, Therapy-Related", "Therapy related acute myeloid leukemia and myelodysplastic syndrome (disorder)", "Therapy related acute myeloid leukemia and myelodysplastic syndrome (diagnosis)", "Therapy-related acute myeloid leukemia and myelodysplastic syndrome (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "therapy related acute myeloid leukemia and myelodysplastic syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0015068", "names": ["Rectal NET", "NET of the rectum", "Rectal Neuroendocrine Tumor", "rectal neuroendocrine tumor", "Rectal neuroendocrine tumor", "neuroendocrine tumor of the rectum", "Neuroendocrine tumor of the rectum", "Neuroendocrine tumour of the rectum", "neuroendocrine tumor of rectum, well differentiated, low or intermediate grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuroendocrine tumor of rectum, well differentiated, low or intermediate grade", "shortest_name_length": 10}
{"curie": "MONDO:0006941", "names": ["Spirillosis", "spirillosis", "Ratbite Fever", "rat bite fever", "Fever, Ratbite", "Rat-bite fever", "rat-bite fever", "bite fever rat", "Rat Bite Fever", "fever rat-bite", "Ratbite Fevers", "Rat-Bite Fever", "Rat bite fever", "rat-bite; fever", "RAT BITE FEVERS", "Rat-bite fevers", "Haverhill Fever", "Rat-Bite Fevers", "Fevers, Ratbite", "fever; rat-bite", "Fever, Rat-Bite", "Fever, Haverhill", "Fevers, Rat-Bite", "rat-bite; disease", "Streptobacillosis", "Rat bite fever, NOS", "Spirillum minus Infection", "Rat bite fever (disorder)", "rat-bite fever (diagnosis)", "Infection, Spirillum minus", "Rat-bite fever unspecified", "Unspecified rat-bite fever", "Spirillum minus Infections", "Rat-bite fever, unspecified", "Infections, Spirillum minus", "Streptobacillus moniliformis Infection", "Streptobacillus moniliformis; infection", "infection; Streptobacillus moniliformis", "Streptobacillus moniliformis Infections", "Infection, Streptobacillus moniliformis", "Infections, Streptobacillus moniliformis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rat-bite fever", "shortest_name_length": 11}
{"curie": "MONDO:0010157", "names": ["Tryptophanuria With Dwarfism", "Tryptophanuria with dwarfism", "TRYPTOPHANURIA WITH DWARFISM", "Tryptophanuria with dwarfism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tryptophanuria with dwarfism", "shortest_name_length": 28}
{"curie": "MONDO:0022553", "names": ["BD syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "BD syndrome", "shortest_name_length": 11}
{"curie": "UMLS:C1336813", "names": ["Transplant-Related Lung Cancer", "Transplant-Related Lung Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transplant-Related Lung Carcinoma", "shortest_name_length": 30}
{"curie": "UMLS:C3272477", "names": ["Ampulla of Vater NET", "Ampulla of Vater Neuroendocrine Tumor", "Neuroendocrine Tumor of the Ampullary Region", "Ampulla of Vater Well Differentiated Endocrine Tumor", "Ampulla of Vater Well Differentiated Endocrine Tumor/Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ampulla of Vater Neuroendocrine Tumor", "shortest_name_length": 20}
{"curie": "UMLS:C0015959", "names": ["Fetal-Maternal Bleed", "FETOMATERNAL BLEEDING", "fetomaternal bleeding", "fetomaternal hemorrhage", "Fetal-maternal bleeding", "Fetomaternal Hemorrhage", "Fetomaternal hemorrhage", "fetomaternal transfusion", "Fetomaternal Hemorrhages", "Fetomaternal transfusion", "Fetomaternal Transfusion", "Fetomaternal haemorrhage", "Hemorrhage, Fetomaternal", "Foetal-maternal bleeding", "Fetal-maternal hemorrhage", "Fetal-Maternal Hemorrhage", "feto maternal transfusion", "fetomaternal; transfusion", "transfusion; fetomaternal", "fetal-maternal hemorrhage", "Hemorrhages, Fetomaternal", "fetal maternal hemorrhage", "Fetomaternal Transfusions", "Fetal maternal hemorrhage", "Transfusion, Fetomaternal", "maternofetal; transfusion", "Foetomaternal haemorrhage", "Transfusions, Fetomaternal", "Fetal maternal haemorrhage", "Fetal-maternal haemorrhage", "hemorrhage; fetal-maternal", "Feto - maternal transfusion", "Foetal-maternal haemorrhage", "Foetal maternal haemorrhage", "Fetal-maternal hemorrhage (disorder)", "fetal-maternal hemorrhage (diagnosis)", "Transplacental fetomaternal hemorrhage", "Transplacental fetomaternal haemorrhage", "Fetal hemorrhage into mother's circulation", "Fetal haemorrhage into mother's circulation", "Foetal haemorrhage into mother's circulation", "fetal; hemorrhage, into, maternal circulation", "Leakage of fetal blood into maternal circulation", "Leakage of foetal blood into maternal circulation", "Fetal blood loss from fetal hemorrhage into mother's circulation", "Fetal-maternal hemorrhage, unspecified as to episode of care in pregnancy", "Fetal-maternal hemorrhage, unspecified as to episode of care or not applicable"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fetomaternal Transfusion", "shortest_name_length": 20}
{"curie": "MONDO:0000764", "names": ["TGFBI corneal dystrophy (disease)", "epithelial-stromal TGFBI dystrophy", "corneal dystrophy (disease) caused by mutation in TGFBI"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epithelial-stromal TGFBI dystrophy", "shortest_name_length": 33}
{"curie": "MONDO:0020376", "names": ["early-onset nuclear cataract", "Cataract, Age-Related Nuclear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early-onset nuclear cataract", "shortest_name_length": 28}
{"curie": "UMLS:C0474874", "names": ["Ectopic Ureterocele", "Ectopic ureterocele", "Ectopic ureterocele (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ectopic ureterocele", "shortest_name_length": 19}
{"curie": "MONDO:0014022", "names": ["MDDGA10", "RXYLT1 muscular dystrophy-dystroglycanopathy, type A", "congenital muscular dystrophy-dystroglycanopathy type A10", "Walker-Warburg syndrome or muscle-eye-brain disease, TMEM5-related", "Walker-Warburg syndrome or muscle-eye-brain disease, Tmem5-related", "WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, TMEM5-RELATED", "muscular dystrophy-dystroglycanopathy, type A caused by mutation in RXYLT1", "congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A10", "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 10", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 10", "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10", "shortest_name_length": 7}
{"curie": "UMLS:C0851954", "names": ["Dental Surface Disorder", "Dental surface disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dental surface disorders", "shortest_name_length": 23}
{"curie": "UMLS:C0686507", "names": ["Metastatic Tumor to the Parathyroid", "Metastasis to the Parathyroid Gland", "Metastatic Neoplasm to the Parathyroid", "parathyroid neoplasm malignant secondary", "Metastatic Tumor to the Parathyroid Gland", "Metastatic Neoplasm to the Parathyroid Gland", "Secondary malignant neoplasm of parathyroid gland", "Metastatic malignant neoplasm to parathyroid gland", "Metastatic malignant neoplasm of parathyroid gland", "Metastatic Malignant Neoplasm to the Parathyroid Glands", "Metastatic Malignant Neoplasm in the Parathyroid Glands", "Secondary malignant neoplasm of parathyroid gland (diagnosis)", "Metastatic malignant neoplasm to parathyroid gland (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to parathyroid gland", "shortest_name_length": 35}
{"curie": "MONDO:0005259", "names": ["ASPG", "Asperger", "Asperger Disease", "asperger syndrome", "Asperger Disorder", "Disease, Asperger", "Asperger Diseases", "Asperger disorder", "asperger disorder", "Aspergers Disease", "Asperger Syndrome", "Asperger syndrome", "Aspergers disorder", "Asperger's Disease", "Asperger Disorders", "Aspergers syndrome", "Syndrome, Asperger", "Disorder, Asperger", "Aspergers Disorder", "Diseases, Asperger", "Aspergers Syndrome", "asperger's syndrome", "Asperger's Diseases", "asperger's disorder", "Asperger's Disorder", "Asperger's Syndrome", "Disorders, Asperger", "Asperger's syndrome", "Asperger's disorder", "Disease, Asperger's", "Diseases, Asperger's", "Syndrome, Asperger's", "Disorder, Asperger's", "Asperger syndrome (diagnosis)", "Schizoid disorder of childhood", "Asperger's disorder (disorder)", "asperger syndrome, susceptibility to", "autism spectrum disorder without disorder of intellectual development and with mild or no impairment of functional language"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Asperger syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0020475", "names": ["dermotrichic syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermotrichic syndrome", "shortest_name_length": 21}
{"curie": "UMLS:C5206451", "names": ["Stage IIIC Cervical Cancer FIGO 2018", "Stage IIIC Cervical Carcinoma FIGO 2018"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Cervical Cancer FIGO 2018", "shortest_name_length": 36}
{"curie": "MONDO:0000872", "names": ["Childhood B-ALL", "childhood B-ALL", "B Cell Childhood ALL", "B cell pediatric ALL", "B-cell childhood ALL", "B cell childhood ALL", "B-Cell Pediatric ALL", "B Cell Pediatric ALL", "B-cell pediatric ALL", "B-Cell Childhood ALL", "pediatric ALL, B cell", "childhood ALL, B-cell", "childhood ALL, B cell", "ALL, childhood B-cell", "B-cell ALL, pediatric", "ALL, pediatric B-cell", "pediatric ALL, B-cell", "B cell ALL, childhood", "B cell ALL, pediatric", "B-cell ALL, childhood", "B Acute Lymphoblastic Leukemia", "B acute lymphoblastic leukemia", "B-cell pediatric acute lymphoid leukemia", "B-Cell Pediatric Acute Lymphoid Leukemia", "childhood B acute lymphoblastic leukemia", "B-cell childhood acute lymphoid leukemia", "Childhood B Acute Lymphoblastic Leukemia", "B-Cell Childhood Acute Lymphoid Leukemia", "B cell pediatric acute lymphocytic leukemia", "B Cell Pediatric Acute Lymphocytic Leukemia", "B-cell pediatric acute lymphocytic leukemia", "B-Cell Childhood Acute Lymphocytic Leukemia", "B Cell Childhood Acute Lymphocytic Leukemia", "B-Cell Pediatric Acute Lymphocytic Leukemia", "B-cell childhood acute lymphocytic leukemia", "B cell childhood acute lymphocytic leukemia", "childhood acute lymphocytic leukemia, B-cell", "acute lymphocytic leukemia, childhood B-cell", "Childhood Precursor B-Lymphoblastic Leukemia", "B-cell acute lymphocytic leukemia, childhood", "B-cell childhood acute lymphogenous leukemia", "pediatric acute lymphocytic leukemia, B-cell", "B cell acute lymphocytic leukemia, childhood", "childhood precursor B-lymphoblastic leukemia", "B-cell pediatric acute lymphogenous leukemia", "B-Cell Pediatric Acute Lymphogenous Leukemia", "B-Cell Childhood Acute Lymphogenous Leukemia", "B-cell childhood acute lymphoblastic leukemia", "B-cell pediatric acute lymphoblastic leukemia", "childhood B-cell acute lymphoblastic leukemia", "B cell pediatric acute lymphoblastic leukemia", "B cell childhood acute lymphoblastic leukemia", "B Cell Pediatric Acute Lymphoblastic Leukemia", "B Cell Childhood Acute Lymphoblastic Leukemia", "B-Cell Pediatric Acute Lymphoblastic Leukemia", "B-Cell Childhood Acute Lymphoblastic Leukemia", "acute lymphoblastic leukemia, childhood B-cell", "childhood acute lymphoblastic leukemia, B-cell", "leukemia, childhood acute lymphocytic leukemia, B-cell", "leukemia, pediatric acute lymphocytic leukemia, B-cell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-cell childhood acute lymphoblastic leukemia", "shortest_name_length": 15}
{"curie": "MONDO:0002220", "names": ["teeth hard tissue disease", "tooth hard tissue disease", "Teeth hard tissue diseases", "teeth hard tissue diseases", "disease of hard tissues of teeth", "Diseases of hard tissues of teeth", "disorder of hard tissues of teeth", "Disorder of hard tissues of teeth", "Disease of hard tissues of teeth, NOS", "dental disorders hard tissues of teeth", "Disorder of hard tissues of teeth (disorder)", "Unspecified disease of hard tissues of teeth", "disease of hard tissues of teeth (diagnosis)", "Disease of hard tissues of teeth, unspecified", "Other specific diseases of hard tissues of teeth", "disease (or disorder); tooth, teeth, hard tissues", "Other specified diseases of hard tissues of teeth", "dental disorders hard tissues of teeth (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tooth hard tissue disease", "shortest_name_length": 25}
{"curie": "UMLS:C2242676", "names": ["Post transplant distal limb syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post transplant distal limb syndrome", "shortest_name_length": 36}
{"curie": "MONDO:0001772", "names": ["anal and rectal ulcer", "Ulcer of anus and rectum", "ulcer of anus and rectum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ulcer of anus and rectum", "shortest_name_length": 21}
{"curie": "MONDO:0009653", "names": ["ML4", "MLIV", "ML 4", "ML IV", "Sialolipidosis", "SIALOLIPIDOSIS", "sialolipidosis", "Sialolipidoses", "mucolipidosis 4", "Berman syndrome", "Mucolipidosis IV", "mucolipidosis IV", "mucolipidosis iv", "MUCOLIPIDOSIS IV", "mucolipidosis; IV", "IV; mucolipidosis", "mucolipidosis type 4", "Mucolipidosis Type IV", "Type IV Mucolipidoses", "mucolipidosis type IV", "Mucolipidosis type IV", "mucolipidosis type iv", "Type IV Mucolipidosis", "Mucolipidoses, Type IV", "Mucolipidosis, Type IV", "Ganglioside sialidase deficiency", "ganglioside sialidase deficiency", "Mucolipidosis type IV (disorder)", "mucolipidosis type iv (diagnosis)", "ganglioside neuraminidase deficiency", "Ganglioside Sialidase Deficiency Disease", "Deficiency Disease, Ganglioside Sialidase"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucolipidosis type IV", "shortest_name_length": 3}
{"curie": "MONDO:0024516", "names": ["ACNINV", "familial acne inversa", "familial hidradenitis suppurativa", "hereditary hidradenitis suppurativa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial acne inversa", "shortest_name_length": 6}
{"curie": "DOID:4586", "names": ["Familial Meningioma", "Familial meningioma", "familial meningioma", "Meningioma, familial", "Hereditary Meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial meningioma", "shortest_name_length": 19}
{"curie": "MONDO:0060763", "names": ["IDDSFTA", "BCL11B-related BAFopathy", "INTELLECTUAL developmental disorder with speech delay, DYSMORPHIC facies, and T-cell abnormalities", "intellectual developmental disorder with dysmorphic facies, speech delay, and t-cell abnormalities", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SPEECH DELAY, AND T-CELL ABNORMALITIES", "intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities", "shortest_name_length": 7}
{"curie": "UMLS:C0338342", "names": ["Recurrent Medulloblastoma", "Relapsed Pediatric Medulloblastoma", "Relapsed Childhood Medulloblastoma", "recurrent pediatric medulloblastoma", "Recurrent Childhood Medulloblastoma", "recurrent childhood medulloblastoma", "recurrent childhood cerebellar PNET", "Recurrent Pediatric Medulloblastoma", "recurrent pediatric cerebellar PNET", "childhood cerebellar PNET, recurrent", "recurrent cerebellar PNET, childhood", "pediatric cerebellar PNET, recurrent", "recurrent cerebellar PNET, pediatric", "recurrent PNET, childhood cerebellar", "recurrent medulloblastoma, childhood", "pediatric medulloblastoma, recurrent", "childhood medulloblastoma, recurrent", "recurrent PNET, pediatric cerebellar", "recurrent medulloblastoma, pediatric", "recurrent cerebellar, childhood, PNET", "PNET, pediatric cerebellar, recurrent", "PNET, childhood cerebellar, recurrent", "recurrent cerebellar, pediatric, PNET", "medulloblastoma, pediatric, recurrent", "medulloblastoma, childhood, recurrent", "PNET, cerebellar, childhood, recurrent", "PNET, cerebellar, pediatric, recurrent", "recurrent pediatric infratentorial PNET", "recurrent childhood infratentorial PNET", "recurrent PNET, childhood infratentorial", "childhood infratentorial PNET, recurrent", "recurrent infratentorial PNET, childhood", "recurrent PNET, pediatric infratentorial", "recurrent infratentorial PNET, pediatric", "pediatric infratentorial PNET, recurrent", "recurrent PNET, infratentorial, pediatric", "recurrent infratentorial, pediatric, PNET", "recurrent PNET, infratentorial, childhood", "recurrent infratentorial, childhood, PNET", "PNET, childhood infratentorial, recurrent", "PNET, pediatric infratentorial, recurrent", "PNET, infratentorial, pediatric, recurrent", "PNET, infratentorial, childhood, recurrent", "recurrent childhood cerebellar primitive neuroectodermal tumor", "recurrent pediatric cerebellar primitive neuroectodermal tumor", "recurrent primitive neuroectodermal tumor, pediatric cerebellar", "recurrent cerebellar primitive neuroectodermal tumor, pediatric", "recurrent cerebellar primitive neuroectodermal tumor, childhood", "recurrent primitive neuroectodermal tumor, childhood cerebellar", "recurrent pediatric infratentorial primitive neuroectodermal tumor", "recurrent childhood infratentorial primitive neuroectodermal tumor", "recurrent infratentorial primitive neuroectodermal tumor, pediatric", "recurrent primitive neuroectodermal tumor, childhood infratentorial", "childhood infratentorial primitive neuroectodermal tumor, recurrent", "recurrent infratentorial primitive neuroectodermal tumor, childhood", "recurrent primitive neuroectodermal tumor, pediatric infratentorial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Medulloblastoma", "shortest_name_length": 25}
{"curie": "UMLS:C0279912", "names": ["Relapsed Urethra Cancer", "Urethra cancer recurrent", "Relapsed Urethral Cancer", "Recurrent Urethra Cancer", "Recurrent Urethral Cancer", "Urethral cancer recurrent", "recurrent urethral cancer", "urethral cancer, recurrent", "Urethral Cancer, Recurrent", "Relapsed Urethra Carcinoma", "Relapsed Cancer of Urethra", "Recurrent Cancer of Urethra", "Recurrent Urethra Carcinoma", "Recurrent Urethral Carcinoma", "Relapsed Cancer of the Urethra", "Recurrent Cancer of the Urethra"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Urethral Cancer", "shortest_name_length": 23}
{"curie": "MONDO:0006826", "names": ["Kwashiokor", "Kwashiorkor", "kwashiorkor", "KWASHIORKOR", "Kwashiorkors", "Protein malnutrition", "protein malnutrition", "PROTEIN MALNUTRITION", "malnutrition; protein", "MALNUTRITION, PROTEIN", "protein; malnutrition", "Kwashiorkor (disorder)", "Deposed child syndrome", "Malignant malnutrition", "kwashiorkor (diagnosis)", "malnutrition; malignant", "malignant; malnutrition", "MALNUTRITION, MALIGNANT", "MALNUTRITION KWASHIORKOR", "NUTRITIONAL EDEMA SYNDROME", "Fatty liver of Brahmin children", "nutritional edema with dyspigmentation of skin and hair", "Nutritional edema with dyspigmentation of skin and hair", "edema; nutritional, with dyspigmentation, skin and hair", "Nutritional oedema with dyspigmentation of skin and hair", "Nutritional edema with dyspigmentation of skin AND/OR hair", "Nutritional oedema with dyspigmentation of skin and/or hair", "Nutritional oedema with dyspigmentation of skin AND/OR hair", "nutritional oedema with dyspigmentation of skin and/or hair", "malnutrition; severe, nutritional edema with dyspigmentation of skin and hair", "severe; malnutrition, nutritional edema with dyspigmentation of skin and hair", "Severe malnutrition with nutritional edema with dyspigmentation of skin and hair"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kwashiorkor", "shortest_name_length": 10}
{"curie": "UMLS:C0155883", "names": ["Chronic obstructive asthma", "Chronic Obstructive Asthma", "chronic obstructive asthma", "chronic obstructive asthma (diagnosis)", "Chronic obstructive asthma (with obstructive pulmonary disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic obstructive asthma (with obstructive pulmonary disease)", "shortest_name_length": 26}
{"curie": "UMLS:C2887084", "names": ["Sepsis due to Streptococcus pneumoniae", "Sepsis caused by Streptococcus pneumoniae", "Sepsis caused by Streptococcus pneumoniae (disorder)", "Severe sepsis with acute organ dysfunction caused by Pneumococcus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sepsis caused by Streptococcus pneumoniae", "shortest_name_length": 38}
{"curie": "UMLS:C0152967", "names": ["sepsis; anaerobic", "anaerobic; sepsis", "anaerobic septicemia", "Anaerobic septicemia", "Anaerobic septicaemia", "Septicemia due to anaerobes", "Septicaemia due to anaerobes", "anaerobic septicemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Septicaemia due to anaerobes", "shortest_name_length": 17}
{"curie": "MONDO:0021479", "names": ["oropharynx benign neoplasm", "Benign Tumor of Oropharynx", "Benign Oropharyngeal Tumor", "benign oropharyngeal tumor", "benign tumor of oropharynx", "Benign tumor of oropharynx", "Benign tumour of oropharynx", "Benign tumor of mesopharynx", "Benign tumour of mesopharynx", "benign neoplasm of oropharynx", "Benign oropharyngeal neoplasm", "Benign neoplasm of oropharynx", "Oropharyngeal Neoplasm Benign", "Oropharyngeal neoplasm benign", "Benign Oropharyngeal Neoplasm", "benign oropharyngeal neoplasm", "oropharyngeal neoplasm benign", "Benign Neoplasm of Oropharynx", "Benign Tumor of the Oropharynx", "benign tumor of the oropharynx", "benign neoplasm of the oropharynx", "Benign Neoplasm of the Oropharynx", "Benign neoplasm of oropharynx, NOS", "Benign neoplasm of oropharynx (disorder)", "benign neoplasm of oropharynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of oropharynx", "shortest_name_length": 26}
{"curie": "UMLS:C5206447", "names": ["Stage IIB Cervical Cancer FIGO 2018", "Stage IIB Cervical Carcinoma FIGO 2018"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Cervical Cancer FIGO 2018", "shortest_name_length": 35}
{"curie": "MONDO:0003117", "names": ["somatoform disorder", "Somatoform Disorder", "disorder somatoform", "Somatoform disorder", "somatoform disorders", "SOMATOFORM DISORDERS", "Somatoform disorders", "Disorder, Somatoform", "psychogenic disorder", "Somatoform Disorders", "psychogenic syndrome", "psychogenic disorders", "psychosomatic disorder", "Psychosomatic disorder", "somatoform disorder NOS", "Somatoform disorder NOS", "Somatoform disorder, NOS", "Psychogenic disorder NOS", "psychophysiologic disorder", "Medically Unexplained Syndrome", "Somatoform disorder (disorder)", "Syndrome, Medically Unexplained", "Unexplained Syndrome, Medically", "Medically Unexplained Syndromes", "somatoform disorder (diagnosis)", "Somatoform disorder, unspecified", "physiological malfunction arising from mental factor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "somatoform disorder", "shortest_name_length": 19}
{"curie": "MONDO:0100467", "names": ["PEE", "PEE1", "PREG1", "Toxemia", "TOXEMIA", "toxemia", "Toxemia NOS", "MATERNAL TOXEMIA", "maternal toxemia", "pregnancy toxemia", "toxemia pregnancy", "toxemia; maternal", "maternal; toxemia", "pregnancy toxaemia", "toxemia; pregnancy", "pregnancy toxemias", "toxaemia pregnancy", "pregnancy; toxemia", "toxemia of pregnancy", "toxemia in pregnancy", "Toxemia of Pregnancy", "Toxemia of pregnancy", "TOXEMIA OF PREGNANCY", "Toxaemia of pregnancy", "toxaemia in pregnancy", "Toxaemia (in);pregnancy", "PREECLAMPSIA/eclampsia 1", "preeclampsia/eclampsia 1", "PREECLAMPSIA/ECLAMPSIA 1", "Toxemia of pregnancy, NOS", "Toxaemia of pregnancy, NOS", "pregnancy toxemia/hypertension", "hypertension, pregnancy-induced", "Hypertensive disorder of pregnancy", "hemolysis, elevated liver enzymes, and low platelet count"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "preeclampsia/eclampsia 1", "shortest_name_length": 3}
{"curie": "MONDO:0011237", "names": ["FCHL1", "HYPLIP1", "hyplip1", "hyperlipidemia, combined, 1", "HYPERLIPIDEMIA, COMBINED, 1", "Hyperlipidemia, Combined, 1", "hyperlipidemia, combined, type 1", "HYPERLIPIDEMIA, FAMILIAL COMBINED, 1", "hyperlipidemia, familial combined, 1", "Hyperlipidemia, Familial Combined, 1", "USF1 familial combined hyperlipidemia", "hyperlipidemia, familial combined, susceptibility to", "familial combined hyperlipidemia caused by mutation in USF1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperlipidemia, combined, 1", "shortest_name_length": 5}
{"curie": "UMLS:C4520760", "names": ["Stage III Larynx Verrucous Carcinoma", "Stage III Verrucous Carcinoma of Larynx", "Stage III Laryngeal Verrucous Carcinoma", "Stage III Laryngeal Throat Verrucous Cancer", "Stage III Verrucous Carcinoma of the Larynx", "Stage III Laryngeal Verrucous Carcinoma AJCC v7", "Stage III Laryngeal Verrucous Carcinoma AJCC v6", "Stage III Laryngeal Verrucous Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Laryngeal Verrucous Carcinoma AJCC v6 and v7", "shortest_name_length": 36}
{"curie": "MONDO:0005942", "names": ["reye syndrome", "Reye syndrome", "REYE SYNDROME", "Reye Syndrome", "syndrome reye", "REYES SYNDROME", "SYNDROME REYES", "reyes syndrome", "Reye's Syndrome", "Reyes' syndrome", "reyes syndromes", "REYE'S SYNDROME", "Reye's syndrome", "reye's syndrome", "reye 's syndrome", "reyes's syndrome", "Reye-Johnson Syndrome", "Reye Johnson Syndrome", "Reye's encephalopathy", "Reye's syndrome (disorder)", "Reye's syndrome (diagnosis)", "FATTY LIVER WITH ENCEPHALOPATHY", "Fatty Liver with Encephalopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reye syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0013396", "names": ["BRMUTD", "Deletion 1p32", "Monosomy 1p32", "Del(1)(p31p32)", "Monosomy 1p31p32", "monosomy 1p31p32", "NFIA-related disorder", "Chromosome 1, monosomy 1p32", "Chromosome 1, Monosomy 1p32", "1p31p32 microdeletion syndrome", "chromosome 1p32-p31 deletion syndrome", "CHROMOSOME 1p32-p31 DELETION SYNDROME", "1p31p32 microdeletion syndrome (disorder)", "brain malformations with or without urinary tract defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 1p32-p31 deletion syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C3897752", "names": ["Recurrent Glioblastoma", "recurrent childhood glioblastoma", "Recurrent Childhood Glioblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Glioblastoma", "shortest_name_length": 22}
{"curie": "MONDO:0019930", "names": ["Leydig cell hypoplasia type I", "46,XY DSD due to complete LH resistance", "46,XY DSD due to complete LH receptor inactivation", "Leydig cell hypoplasia due to complete LH resistance", "46,XY DSD due to complete luteinizing hormone resistance", "Leydig cell hypoplasia due to complete LH receptor inactivation", "46,XY disorder of sex development due to complete LH resistance", "46,XY DSD due to complete luteinizing hormone receptor inactivation", "Leydig cell hypoplasia due to complete luteinizing hormone resistance", "46,XY disorder of sex development due to complete LH receptor inactivation", "46,XY disorder of sex development due to complete luteinizing hormone resistance", "Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation", "46,XY disorder of sex development due to complete luteinizing hormone receptor inactivation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leydig cell hypoplasia due to complete LH resistance", "shortest_name_length": 29}
{"curie": "MONDO:0012894", "names": ["OS6", "OA knee", "Gonarthrosis", "Osteoarthritis knee", "Osteoarthritis;knee", "Knee Osteoarthritis", "knee osteoarthrosis", "osteoarthritis knee", "Knee osteoarthritis", "knee osteoarthritis", "Osteoarthritis knees", "Osteoarthritis, Knee", "Osteo arthritis knees", "Knee Osteoarthritides", "osteoarthritis of knee", "OSTEOARTHRITIS OF KNEE", "osteoarthrosis of knee", "Osteoarthrosis of knee", "Osteoarthritis of knee", "Osteoarthritis of Knee", "osteoarthritis of the knee", "Osteoarthritis of the Knee", "OA - Osteoarthritis of knee", "osteoarthritis susceptibility 6", "OSTEOARTHRITIS SUSCEPTIBILITY 6", "Osteoarthritis of knee (disorder)", "osteoarthrosis of knee (diagnosis)", "osteoarthritis of knee (diagnosis)", "Degenerative joint disease of knee", "Osteoarthritis of knee, unspecified", "Knee DJD (degenerative joint disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteoarthritis susceptibility 6", "shortest_name_length": 3}
{"curie": "MONDO:0000118", "names": ["reticulate pigment disorder", "reticulate pigment disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "reticulate pigment disorder", "shortest_name_length": 27}
{"curie": "UMLS:C3805057", "names": ["Vein collapse"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vein collapse", "shortest_name_length": 13}
{"curie": "MONDO:0008402", "names": ["Say syndrome", "SAY SYNDROME", "SAY syndrome", "Say Barber Hobbs syndrome", "Say-Barber-Hobbs syndrome", "cleft palate large ears small head", "Cleft palate large ears small head", "cleft palate-large ears-small head syndrome", "Cleft palate-large ears-small head syndrome", "Cleft palate, large ears, small head syndrome", "Cleft palate, large ears, small head syndrome (disorder)", "CLEFT PALATE, MICROCEPHALY, LARGE EARS, AND SHORT STATURE", "Cleft palate, microcephaly, large ears, and short stature", "cleft palate, microcephaly, large ears, and short stature"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleft palate-large ears-small head syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0001085", "names": ["T.I.N., NOS", "INTERSTITIAL NEPHRITIS", "NEPHRITIS INTERSTITIAL", "Interstitial Nephritis", "nephritis interstitial", "Interstitial nephritis", "Nephritis interstitial", "interstitial nephritis", "Nephritis, Interstitial", "Nephritis, interstitial", "Interstitial Nephritides", "Nephritides, Interstitial", "disease tubulointerstitial", "tubulointerstitial disease", "Interstitial nephritis NOS", "Tubulointerstitial Disease", "Tubulointerstitial disease", "IN - Interstitial nephritis", "TUBULOINTERSTITIAL DISEASES", "Interstitial nephritis, NOS", "Tubulointerstitial nephritis", "tubulo-interstitial; disease", "tubulointerstitial nephritis", "Tubulointerstitial Nephritis", "Tubulo-interstitial nephritis", "Nephritis, Tubulointerstitial", "nephritis; tubulo-interstitial", "Tubulointerstitial nephropathy", "tubulointerstitial nephropathy", "Tubulointerstitial Nephritides", "tubulo-interstitial; nephritis", "Nephritides, Tubulointerstitial", "NEPHROPATHY, TUBULOINTERSTITIAL", "renal tubulo-interstitial disease", "Renal tubulo-interstitial disease", "interstitial nephritis (diagnosis)", "Renal tubulo-interstitial diseases", "Tubulointerstitial nephropathy, NOS", "Interstitial renal disease or syndrome", "Tubulointerstitial nephritis (disorder)", "Interstitial nephritis (qualifier value)", "Tubulointerstitial nephropathy (disorder)", "Interstitial Renal Diseases and Syndromes", "renal; disease, with interstitial nephritis", "Renal tubulo-interstitial diseases (N10-N16)", "renal tubulo-interstitial disease (diagnosis)", "Renal tubulo-interstitial disease, unspecified", "disease (or disorder); tubulo-interstitial (in)", "disease (or disorder); renal, with interstitial nephritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "interstitial nephritis", "shortest_name_length": 11}
{"curie": "MONDO:0004102", "names": ["columnar cell variant papillary carcinoma", "Columnar Cell Variant Papillary Carcinoma", "Papillary Thyroid Carcinoma, Columnar Variant", "columnar cell variant papillary thyroid gland carcinoma", "Columnar Cell Variant Papillary Thyroid Gland Carcinoma", "columnar cell variant thyroid gland papillary carcinoma", "Columnar Cell Variant Thyroid Gland Papillary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "columnar cell variant thyroid gland papillary carcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0010959", "names": ["VDEGS", "Van den Ende Gupta syndrome", "Van den Ende-Gupta syndrome", "van den Ende-Gupta syndrome", "Marden Walker like syndrome", "Van Den Ende-Gupta Syndrome", "VAN DEN Ende-Gupta syndrome", "VAN DEN ENDE-GUPTA SYNDROME", "Marden-Walker-like syndrome", "Van den Ende-Gupta syndrome (disorder)", "Marden-Walker-like syndrome without psychmotor retardation", "Marden-Walker-Like Syndrome Without Psychomotor Retardation", "Marden Walker like syndrome without psychomotor retardation", "Marden-Walker-like syndrome without psychomotor retardation", "MARDEN-WALKER-LIKE SYNDROME WITHOUT PSYCHOMOTOR RETARDATION", "BLEPHAROPHIMOSIS, ARACHNODACTYLY, AND CONGENITAL CONTRACTURES", "blepharophimosis, arachnodactyly, and congenital contractures", "Blepharophimosis, arachnodactyly, and congenital contractures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "van den Ende-Gupta syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0001287", "names": ["scar endometriosis", "Scar endometriosis", "endometriosis in scar", "endometriosis in scar of skin", "Endometriosis in scar of skin", "endometriosis in cutaneous scar", "Endometriosis in cutaneous scar", "endometriosis in scar (diagnosis)", "Endometriosis in scar of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometriosis in cutaneous scar", "shortest_name_length": 18}
{"curie": "UMLS:C4744380", "names": ["Malignant Skull Base Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Skull Base Neoplasm", "shortest_name_length": 29}
{"curie": "MONDO:0016928", "names": ["Duplication of chromosome 7", "partial trisomy of chromosome 7", "Partial trisomy of chromosome 7", "partial duplication of chromosome 7", "Partial duplication of chromosome 7", "partial duplication of chromosome type 7", "Partial trisomy of chromosome 7 (disorder)", "Partial trisomy of chromosome 7 (diagnosis)", "anomaly of chromosome pair 7 partial trisomy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of chromosome 7", "shortest_name_length": 27}
{"curie": "MONDO:0013101", "names": ["BCC2", "basal cell carcinoma, susceptibility to, 2", "BASAL CELL CARCINOMA, SUSCEPTIBILITY TO, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "basal cell carcinoma, susceptibility to, 2", "shortest_name_length": 4}
{"curie": "UMLS:C1332244", "names": ["Ampullary Adenoma", "Ampulla of Vater Adenoma", "Adenoma of ampulla of Vater", "Adenoma of ampulla of Vater (disorder)", "Ampulla of Vater Intestinal-Type Adenoma", "Ampulla of Vater Adenoma, Intestinal-Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenoma of ampulla of Vater", "shortest_name_length": 17}
{"curie": "MONDO:0018257", "names": ["familial syringomyelia", "hereditary syringomyelia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial syringomyelia", "shortest_name_length": 22}
{"curie": "MONDO:0016731", "names": ["DIA/DIG", "desmoplastic infantile astrocytoma/ganglioglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "desmoplastic infantile astrocytoma/ganglioglioma", "shortest_name_length": 7}
{"curie": "MONDO:0018180", "names": ["staphylococcal scarlet fever"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "staphylococcal scarlet fever", "shortest_name_length": 28}
{"curie": "UMLS:C4725869", "names": ["Unresectable Undifferentiated Pleomorphic Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Undifferentiated Pleomorphic Sarcoma", "shortest_name_length": 49}
{"curie": "MONDO:0700100", "names": ["leukemia, non-human animal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukemia, non-human animal", "shortest_name_length": 26}
{"curie": "MONDO:0016169", "names": ["CADP", "chronic acquired peripheral neuropathy", "acquired peripheral neuropathy, chronic", "chronic acquired demyelinating polyneuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic acquired demyelinating polyneuropathy", "shortest_name_length": 4}
{"curie": "UMLS:C0686763", "names": ["Bifid ossification", "Bipartite Ossification", "BIPARTITE OSSIFICATION", "Bipartite ossification", "Bipartite ossification (finding)", "Bipartite ossification (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bipartite ossification", "shortest_name_length": 18}
{"curie": "UMLS:C4288049", "names": ["Uterine Corpus Hydropic Leiomyoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Corpus Hydropic Leiomyoma", "shortest_name_length": 33}
{"curie": "MONDO:0003824", "names": ["familial renal oncocytoma", "Familial Renal Oncocytoma", "hereditary renal oncocytoma", "Hereditary Renal Oncocytoma", "Hereditary Kidney Oncocytoma", "hereditary kidney oncocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary kidney oncocytoma", "shortest_name_length": 25}
{"curie": "UMLS:C2981636", "names": ["Stage IIIB Hilar Cholangiocarcinoma", "Stage IIIB Hilar Cholangiocarcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Hilar Cholangiocarcinoma AJCC v7", "shortest_name_length": 35}
{"curie": "MONDO:0007782", "names": ["farmer syndrome", "FARMER SYNDROME", "Farmer Syndrome", "hyperthermia, cutaneous, with headaches and nausea", "Hyperthermia, Cutaneous, With Headaches And Nausea", "HYPERTHERMIA, CUTANEOUS, WITH HEADACHES AND NAUSEA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperthermia, cutaneous, with headaches and nausea", "shortest_name_length": 15}
{"curie": "MONDO:0007060", "names": ["SPGF6", "GLOBOZOOSPERMIA", "globozoospermia", "Globozoospermia", "Globozoospermias", "SPATA16 azoospermia", "Spermatozoa.round head", "Spermatozoa Round Head", "SPERMATOGENIC FAILURE 6", "spermatogenic failure 6", "round-headed spermatozoa", "ROUND-HEADED SPERMATOZOA", "Round-headed spermatozoa", "SPERMATOZOA, ROUND-HEADED", "spermatozoa, round-headed", "Globozoospermia (disorder)", "spermatogenic failure type 6", "ACROSOME MALFORMATION OF SPERMATOZOA", "acrosome malformation of spermatozoa", "azoospermia caused by mutation in SPATA16"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 6", "shortest_name_length": 5}
{"curie": "MONDO:0007901", "names": ["OCLEVS", "oculomotor-levator synkinesis", "OCULOMOTOR-LEVATOR SYNKINESIS", "Oculomotor-Levator Synkinesis", "levator-medial rectus synkinesis", "LEVATOR-MEDIAL RECTUS SYNKINESIS", "Levator-medial rectus synkinesis", "Levator-Medial Rectus Synkinesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "levator-medial rectus synkinesis", "shortest_name_length": 6}
{"curie": "MONDO:0019608", "names": ["46,XX DSD induced by maternal-derived androgen", "46,XX disorder of sex development induced by maternal-derived androgen"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XX disorder of sex development induced by maternal-derived androgen", "shortest_name_length": 46}
{"curie": "MONDO:0008212", "names": ["Dynia factor deficiency", "DYNIA FACTOR DEFICIENCY", "Dynia Factor Deficiency", "Pechet factor deficiency", "Pechet Factor Deficiency", "PECHET FACTOR DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pechet factor deficiency", "shortest_name_length": 23}
{"curie": "UMLS:C0333145", "names": ["HEMATOCYST", "Blood cyst", "Hematocyst", "cyst blood", "blood cyst", "hematocyst", "Haematocyst", "blood cysts", "Hemorrhagic Cyst", "hemorrhagic cyst", "cyst hemorrhagic", "Hemorrhagic cyst", "Cyst, hemorrhagic", "Haemorrhagic cyst", "haemorrhagic cyst", "cysts hemorrhagic", "Hemorrhagic cyst (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemorrhagic cyst", "shortest_name_length": 10}
{"curie": "UMLS:C0949177", "names": ["White spot lesion", "White Spot Lesion", "white spot; lesion", "lesion; white spot", "white; spot lesions", "spot lesions; white"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "White Spot Lesion", "shortest_name_length": 17}
{"curie": "UMLS:C4683748", "names": ["Stage IV Mycosis Fungoides and Sezary Syndrome AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Mycosis Fungoides and Sezary Syndrome AJCC v8", "shortest_name_length": 54}
{"curie": "MONDO:0024873", "names": ["clitoral cancer", "Clitoral Cancer", "Clitoral Carcinoma", "clitoris carcinoma", "clitoral carcinoma", "Clitoris Carcinoma", "carcinoma of clitoris", "Carcinoma of Clitoris", "carcinoma of the clitoris", "Carcinoma of the Clitoris"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "clitoral carcinoma", "shortest_name_length": 15}
{"curie": "UMLS:C3495829", "names": ["Chronic pigmented purpura"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic pigmented purpura", "shortest_name_length": 25}
{"curie": "MONDO:0011765", "names": ["MED5", "EDM5", "BHMED", "Polyepiphyseal dysplasia type 5", "Multiple epiphyseal dysplasia 5", "multiple epiphyseal dysplasia 5", "epiphyseal dysplasia multiple 5", "epiphyseal dysplasia, multiple, 5", "EPIPHYSEAL DYSPLASIA, MULTIPLE, 5", "Epiphyseal dysplasia, multiple, 5", "Multiple epiphyseal dysplasia type 5", "multiple epiphyseal dysplasia type 5", "epiphyseal dysplasia, multiple, type 5", "multiple epiphyseal dysplasia MATN3-related", "MULTIPLE EPIPHYSEAL DYSPLASIA, MATN3-RELATED", "multiple epiphyseal dysplasia, MATN3-related", "Multiple epiphyseal dysplasia, MATN3 related", "Multiple Epiphyseal Dysplasia, Matn3-Related", "multiple epiphyseal dysplasia, MATN3 related", "MATN3 multiple epiphyseal dysplasia (disease)", "bilateral hereditary microepiphyseal dysplasia", "Microepiphyseal Dysplasia, Bilateral Hereditary", "Multiple epiphyseal dysplasia type 5 (disorder)", "Microepiphyseal dysplasia, bilateral hereditary", "bilateral hereditary micro-epiphyseal dysplasia", "Bilateral hereditary micro-epiphyseal dysplasia", "MICROEPIPHYSEAL DYSPLASIA, BILATERAL HEREDITARY", "multiple epiphyseal dysplasia (disease) caused by mutation in MATN3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple epiphyseal dysplasia type 5", "shortest_name_length": 4}
{"curie": "UMLS:C4331317", "names": ["Stage I Nasopharyngeal Throat Cancer", "Stage I Nasopharyngeal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Nasopharyngeal Carcinoma AJCC v8", "shortest_name_length": 36}
{"curie": "MONDO:0009521", "names": ["leukemia, acute myelocytic, with polyposis coli and colon cancer", "Leukemia, Acute Myelocytic, with Polyposis Coli and Colon Cancer", "LEUKEMIA, ACUTE MYELOCYTIC, WITH POLYPOSIS COLI AND COLON CANCER"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukemia, acute myelocytic, with polyposis coli and colon cancer", "shortest_name_length": 64}
{"curie": "MONDO:0017779", "names": ["NAGA deficiency", "Schindler disease", "alpha-N-acetylgalactosaminidase deficiency", "alpha-N-acetylgalactosaminidase activity disease", "disorder of alpha-N-acetylgalactosaminidase activity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alpha-N-acetylgalactosaminidase deficiency", "shortest_name_length": 15}
{"curie": "MONDO:0016787", "names": ["ETT", "epithelioid trophoblastic tumor", "Epithelioid trophoblastic tumor", "Epithelioid Trophoblastic Tumor", "Trophoblastic tumor, epithelioid", "Epithelioid trophoblastic tumour", "Trophoblastic tumour, epithelioid", "malignant epithelioid trophoblastic tumor", "Epithelioid trophoblastic tumor (disorder)", "malignant epithelioid trophoblastic tumor (diagnosis)", "Trophoblastic tumor, epithelioid (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epithelioid trophoblastic tumor", "shortest_name_length": 3}
{"curie": "MONDO:0016558", "names": ["CMM", "mirror movement", "mirror movements", "Mirror movements", "bimanual synkinesis", "Bimanual synkinesia", "Mirror hand movements", "Hand mirror movements", "mirror movement disorder", "Mirror movements (disorder)", "congenital mirror movements", "congenital mirror movement disorder", "familial congenital mirror movements", "isolated congenital mirror movements", "hereditary congenital mirror movements", "isolated congenital controlateral synkinesia", "familial congenital controlateral synkinesia", "hereditary congenital controlateral synkinesia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial congenital mirror movements", "shortest_name_length": 3}
{"curie": "MONDO:0033638", "names": ["MC4DN8", "mitochondrial complex 4 deficiency, nuclear type 8", "MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 8", "mitochondrial complex IV deficiency, nuclear type 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 4 deficiency, nuclear type 8", "shortest_name_length": 6}
{"curie": "UMLS:C5237017", "names": ["Recurrent Diffuse Large B-Cell Lymphoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Diffuse Large B-Cell Lymphoma, Not Otherwise Specified", "shortest_name_length": 64}
{"curie": "EFO:0009761", "names": ["periprosthetic osteolysis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "periprosthetic osteolysis", "shortest_name_length": 25}
{"curie": "MONDO:0008194", "names": ["BOLK CUSP", "bolk cusp", "Bolk cusp", "Tuberculum paramolare", "tuberculum paramolare", "paramolare; tuberculum", "tuberculum; paramolare", "PARAMOLAR TUBERCLE OF BOLK", "Paramolar tubercle of bolk", "Tuberculum paramolare (disorder)", "tuberculum paramolare (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paramolar tubercle of bolk", "shortest_name_length": 9}
{"curie": "UMLS:C5419178", "names": ["COVID-19-Associated Acute Liver Injury", "SARS-CoV-2-Associated Acute Liver Injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "COVID-19-Associated Acute Liver Injury", "shortest_name_length": 38}
{"curie": "MONDO:0002113", "names": ["peritoneal carcinoma", "peritoneum carcinoma", "carcinoma of peritoneum", "Carcinoma of peritoneum", "primary peritoneal carcinoma", "Malignant epithelial neoplasm of peritoneum", "Malignant epithelial neoplasm of peritoneum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peritoneal carcinoma", "shortest_name_length": 20}
{"curie": "UMLS:C5238327", "names": ["Obesity-Related Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Obesity-Related Malignant Neoplasm", "shortest_name_length": 34}
{"curie": "MONDO:0012203", "names": ["Nonautoimmune hyperthyroidism", "nonautoimmune hyperthyroidism", "HYPERTHYROIDISM, NONAUTOIMMUNE", "Hyperthyroidism, Nonautoimmune", "hyperthyroidism, NONAUTOIMMUNE", "THYROTROPIN RECEPTOR POLYMORPHISM", "Thyroid Adenoma, Hyperfunctioning", "THYROID ADENOMA, HYPERFUNCTIONING", "familial non-immune hyperthyroidism", "THYROID CARCINOMA WITH THYROTOXICOSIS", "Thyroid Carcinoma With Thyrotoxicosis", "Congenital nonautoimmune hyperthyroidism", "Hyperthyroidism, Congenital Nonautoimmune", "hyperthyroidism, congenital Nonautoimmune", "resistance to thyroid stimulating hormone", "nonautoimmune hyperthyroidism (diagnosis)", "HYPERTHYROIDISM, CONGENITAL NONAUTOIMMUNE", "THYROID ADENOMA, HYPERFUNCTIONING, SOMATIC", "TOXIC THYROID HYPERPLASIA, AUTOSOMAL DOMINANT", "Toxic Thyroid Hyperplasia, Autosomal Dominant", "toxic thyroid hyperplasia, autosomal dominant", "THYROID CARCINOMA WITH THYROTOXICOSIS, SOMATIC", "hyperthyroidism, Nonautoimmune, autosomal dominant", "Hyperthyroidism, Nonautoimmune, Autosomal Dominant", "HYPERTHYROIDISM, NONAUTOIMMUNE, AUTOSOMAL DOMINANT", "familial hyperthyroidism due to mutations in TSH receptor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial hyperthyroidism due to mutations in TSH receptor", "shortest_name_length": 29}
{"curie": "MONDO:0009840", "names": ["Partington-Anderson Syndrome", "Partington Anderson syndrome", "Partington-Anderson syndrome", "PARTINGTON-ANDERSON SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Partington-Anderson syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0016075", "names": ["Filariases", "Filariasis", "filariases", "Filariosis", "FILARIASIS", "filariasis", "filariosis", "Filarioidea Infection", "Elephantiasis tropica", "filariasis (diagnosis)", "Infection, Filarioidea", "Filarioidea Infections", "Unspecified filariasis", "Filariasis, unspecified", "Infections, Filarioidea", "disease due to superfamily Filarioidea", "Disease due to superfamily Filarioidea", "DISEASES DUE TO SUPERFAMILY FILARIOIDEA", "Disease caused by superfamily Filarioidea", "Disease caused by superfamily Filarioidea (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "filariasis", "shortest_name_length": 10}
{"curie": "MONDO:0012637", "names": ["CDG2G", "CDGIIG", "CDGIIg", "CDG 2G", "CDG-IIg", "CDG IIg", "CDG IIG", "COG1-CDG", "COG1-CDG (CDG-IIg)", "CDG syndrome type IIg", "COG1 congenital disorder of glycosylation", "COG1-congenital disorder of glycosylation", "Congenital disorder of glycosylation type 2g", "congenital disorder of glycosylation type 2g", "Congenital disorder of glycosylation type IIg", "congenital disorder of glycosylation type IIg", "Congenital disorder of glycosylation, type 2G", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg", "congenital disorder of glycosylation, type IIg", "Congenital Disorder Of Glycosylation, Type IIG", "CDGII/COG1 CEREBROCOSTOMANDIBULAR-LIKE SYNDROME", "Cdgii/Cog1 Cerebrocostomandibular-like syndrome", "CDGII/COG1 cerebrocostomandibular-like syndrome", "Carbohydrate deficient glycoprotein syndrome type 2g", "Carbohydrate deficient glycoprotein syndrome type IIg", "carbohydrate deficient glycoprotein syndrome type IIg", "CDG2G - carbohydrate deficient glycoprotein syndrome type 2G", "Component of oligomeric golgi complex 1 congenital disorder of glycosylation", "COG1 (component of oligomeric golgi complex 1) congenital disorder of glycosylation", "Component of oligomeric golgi complex 1 congenital disorder of glycosylation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "COG1-congenital disorder of glycosylation", "shortest_name_length": 5}
{"curie": "MONDO:0004970", "names": ["ADNOS", "Adenocarcinoma", "adenocarcinoma", "ADENOCARCINOMA", "adenocarcinomas", "Adenocarcinomas", "Malignant Adenoma", "ADENOCARCINOMA NOS", "Malignant Adenomas", "Adenoma, Malignant", "Adenocarcinoma NOS", "Adenomas, Malignant", "Adenocarcinoma, NOS", "Carcinoma in adenoma", "adenocarcinoma, malignant", "ADENOCARCINOMA, MALIGNANT", "adenocarcinoma (diagnosis)", "Malignant adenomatous neoplasm", "malignant adenomatous neoplasm", "Adenocarcinoma (morphologic abnormality)", "Malignant adenomatous neoplasm (disorder)", "malignant adenomatous neoplasm (diagnosis)", "adenocarcinoma NOS (morphologic abnormality)", "adenocarcinoma, no subtype (morphologic abnormality)", "Malignant adenomatous neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenocarcinoma", "shortest_name_length": 5}
{"curie": "MONDO:0001119", "names": ["POF", "menopause early", "early menopause", "Early menopause", "Menopause praecox", "menopause praecox", "Menopause, praecox", "Premature menopause", "PREMATURE MENOPAUSE", "MENOPAUSE PREMATURE", "premature menopause", "menopause premature", "Premature;menopause", "Premature Menopause", "Menopause premature", "Climacterium praecox", "Menopause, Premature", "Menopause, premature", "premature; menopausal", "menopausal; premature", "menopause - premature", "Menopause - premature", "Premature menopause NOS", "Premature Ovarian Failure", "Premature ovarian failure", "premature ovarian failure", "Hypergonadotropic amenorrhea", "Premature menopause (finding)", "Primary ovarian insufficiency", "Premature ovarian insufficiency", "premature menopause (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "premature menopause", "shortest_name_length": 3}
{"curie": "UMLS:C0862326", "names": ["Recurrent Malignant Bladder Neoplasm", "Malignant neoplasm of bladder recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant neoplasm of bladder recurrent", "shortest_name_length": 36}
{"curie": "UMLS:C5418829", "names": ["Unresectable Thyroid Gland Anaplastic Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Thyroid Gland Anaplastic Carcinoma", "shortest_name_length": 47}
{"curie": "MONDO:0014905", "names": ["EMPF2", "Leigh-like encephalopathy-optic atrophy-peripheral neuropathy syndrome", "ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2", "encephalopathy due to defective mitochondrial and peroxisomal fission 2", "encephalopathy due to defective mitochondrial and peroxisomal fission type 2", "Leigh-like basal ganglia disease-optic atrophy-peripheral neuropathy syndrome", "MFF-related encephalopathy due to mitochondrial and peroxisomal fission defect", "MFF-associated encephalopathy due to peroxisomal and mitochondrial fission defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephalopathy due to defective mitochondrial and peroxisomal fission 2", "shortest_name_length": 5}
{"curie": "MONDO:0008189", "names": ["Erosive Adenomatosis", "erosive; adenomatosis", "florid papillomatosis", "adenomatosis; erosive", "Erosive Nipple Adenomatosis", "erosive nipple adenomatosis", "erosive adenomatosis of nipple", "Erosive adenomatosis of nipple", "papillomatosis florid of nipple", "papillomatosis, florid, of nipple", "PAPILLOMATOSIS, FLORID, OF NIPPLE", "Papillomatosis, Florid, of Nipple", "Erosive Adenomatosis of the Nipple", "erosive adenomatosis of the nipple", "Erosive adenomatosis of the nipple", "florid papillomatosis of the nipple", "Florid Papillomatosis of the Nipple", "EAN - erosive adenomatosis of nipple", "Erosive adenomatosis of nipple (disorder)", "[OBSOLETE] Papillomatosis, florid, of nipple"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papillomatosis, florid, of nipple", "shortest_name_length": 20}
{"curie": "UMLS:C5206593", "names": ["Paratesticular Wilms Tumor", "Paratesticular Nephroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paratesticular Wilms Tumor", "shortest_name_length": 26}
{"curie": "UMLS:C0752288", "names": ["Adjustment Sleep Disorder", "Sleep Disorder, Adjustment", "Adjustment Sleep Disorders", "Sleep Disorders, Adjustment"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adjustment Sleep Disorder", "shortest_name_length": 25}
{"curie": "UMLS:C3658208", "names": ["Dysbiosis", "Disbioses", "Disbiosis", "Dysbioses", "Dys-symbiosis", "Dys symbiosis", "Dys-symbioses"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dysbiosis", "shortest_name_length": 9}
{"curie": "MONDO:0016759", "names": ["PCH2", "pontocerebellar hypoplasia type 2", "Pontocerebellar Hypoplasia Type 2", "Pontocerebellar hypoplasia type 2", "PCH2 - pontocerebellar hypoplasia type 2", "Congenital pontocerebellar hypoplasia type 2", "Congenital pontocerebellar hypoplasia type 2 (disorder)", "progressive microcephaly from birth extrapyramidal dyskinesia chorea epilepsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pontocerebellar hypoplasia type 2", "shortest_name_length": 4}
{"curie": "UMLS:C4331894", "names": ["Hypothyroid Goiter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypothyroid Goiter", "shortest_name_length": 18}
{"curie": "MONDO:0011215", "names": ["GCLEB", "Habrodysplasia", "HABRODYSPLASIA", "OSTEOCRANIOSTENOSIS", "Osteocraniostenosis", "osteocraniostenosis", "Gracile bone dysplasia", "GRACILE BONE DYSPLASIA", "gracile bone dysplasia", "Osteocraniosplenic syndrome", "OSTEOCRANIOSPLENIC SYNDROME", "Osteocraniostenosis (disorder)", "skeletal dysplasia lethal with gracile bones", "skeletal dysplasia, lethal, with gracile bones", "Skeletal dysplasia, lethal, with gracile bones", "SKELETAL DYSPLASIA, LETHAL, WITH GRACILE BONES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteocraniostenosis", "shortest_name_length": 5}
{"curie": "MONDO:0029148", "names": ["SPGF34", "spermatogenic failure 34", "SPERMATOGENIC FAILURE 34"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 34", "shortest_name_length": 6}
{"curie": "UMLS:C4086168", "names": ["Childhood Ovarian Nongerminomatous Germ Cell Tumor", "Childhood Ovarian Non-Germinomatous Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Ovarian Nongerminomatous Germ Cell Tumor", "shortest_name_length": 50}
{"curie": "UMLS:C4764216", "names": ["Refractory Paraganglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Paraganglioma", "shortest_name_length": 24}
{"curie": "UMLS:C0877157", "names": ["pancreas transplant rejection", "Pancreas transplant rejection", "pancreas transplant; rejection", "rejection; transplant, pancreas", "Rejection of pancreas transplant", "rejection of transplanted pancreas", "pancreas transplant rejection (diagnosis)", "Rejection of pancreas transplant (disorder)", "rejection of transplanted pancreas (treatment)", "pancreatic transplant post-transplant dysfunction rejection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rejection of pancreas transplant", "shortest_name_length": 29}
{"curie": "MONDO:0001215", "names": ["petriellidosis", "allescheriasis", "Allescheriosis", "Allescheriasis", "Petriellidosis", "ALLESCHERIOSIS", "allescheriosis", "Pseudallescheriosis", "Allescheriosis (disorder)", "petriellidosis (diagnosis)", "allescheriasis (diagnosis)", "infection; Allescheria boydii", "Allescheria boydii; infection", "Petriellidium boydii; infection", "Allescheriosis (Petriellidosis)", "Allescheriosis [Petriellidosis]", "infection; Petriellidium boydii", "Infection by Allescheria boydii", "Infections by Allescheria boydii", "Infection by Petriellidium boydii", "Infections by Petriellidium boydii"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "allescheriosis", "shortest_name_length": 14}
{"curie": "MONDO:0007828", "names": ["MARSIS", "MARSILI syndrome", "Marsili syndrome", "MARSILI SYNDROME", "congenital analgesia", "congenital insensitivity to pain", "congenital analgesia, autosomal dominant", "Congenital Analgesia, Autosomal Dominant", "CONGENITAL ANALGESIA, AUTOSOMAL DOMINANT", "indifference to pain, congenital, autosomal dominant", "Indifference to Pain, Congenital, Autosomal Dominant", "insensitivity to pain, congenital, autosomal dominant", "INSENSITIVITY TO PAIN, CONGENITAL, AUTOSOMAL DOMINANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "indifference to pain, congenital, autosomal dominant", "shortest_name_length": 6}
{"curie": "MONDO:0015480", "names": ["Cleft upper eyelid", "Notched upper eyelid", "Upper eyelid coloboma", "Upper eyelid colobomas", "Coloboma of upper eyelid", "Superior palpebral coloboma", "superior palpebral coloboma", "coloboma of superior eyelid", "Coloboma of superior eyelid", "Coloboma of the upper eyelid", "congenital eyelid coloboma superior", "Coloboma of superior eyelid (disorder)", "Coloboma of superior eyelid (diagnosis)", "Full thickness defect of the upper eyelid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coloboma of superior eyelid", "shortest_name_length": 18}
{"curie": "UMLS:C0018779", "names": ["psychogenic deafness", "Psychogenic deafness", "Deafness, psychogenic", "Nonorganic Hearing Loss", "Functional Hearing Loss", "functional hearing loss", "Functional hearing loss", "Hearing Loss, Functional", "Hearing Loss, Nonorganic", "Non-organic hearing loss", "Psychogenic Hearing Loss", "non-organic hearing loss", "Hearing Loss, Psychogenic", "FHL - Functional hearing loss", "Psychogenic deafness (disorder)", "NOHL - Non-organic hearing loss"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hearing Loss, Functional", "shortest_name_length": 20}
{"curie": "UMLS:C1333464", "names": ["Esophagus Non-Hodgkin Lymphoma", "Esophageal Non-Hodgkin Lymphoma", "Non-Hodgkin's Esophagus Lymphoma", "Esophageal Non-Hodgkin's Lymphoma", "Non-Hodgkin's Lymphoma of Esophagus", "Non-Hodgkin's Lymphoma of the Esophagus", "Primary Esophageal Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Non-Hodgkin Lymphoma", "shortest_name_length": 30}
{"curie": "UMLS:C5208295", "names": ["SJS-TEN overlap"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SJS-TEN overlap", "shortest_name_length": 15}
{"curie": "MONDO:0021095", "names": ["Parkinsonism", "parkinsonism", "PARKINSONISM", "parkinsonisms", "Parkinsonism, NOS", "parkinsonian disease", "Parkinsonian disease", "parkinsonian syndrome", "Parkinsonian symptoms", "Parkinsonian Syndrome", "SYNDROME PARKINSONISM", "parkinsonian disorder", "PARKINSONIAN SYNDROME", "Parkinsonian Symptoms", "Parkinsonian Diseases", "parkinsonian syndromes", "Parkinsonian Syndromes", "parkinsonian disorders", "Parkinsonian Disorders", "Parkinsonism (disorder)", "Parkinsonism (diagnosis)", "Hypokinetic-rigid syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parkinsonian disorder", "shortest_name_length": 12}
{"curie": "MONDO:0009475", "names": ["IVA", "IVD deficiency", "IVD DEFICIENCY", "Isovalericacidemia", "isovaleric acidemia", "Isovaleric acidemia", "isovaleric aciduria", "ISOVALERIC ACIDEMIA", "Isovaleric Acidemia", "Isovaleric acidaemia", "isovaleric; acidemia", "acidemia; isovaleric", "Acidemia, isovaleric", "isovaleric acidemia (diagnosis)", "Isovaleryl CoA carboxylase deficiency", "isovaleryl CoA carboxylase deficiency", "Isovaleryl-CoA Dehydrogenase Deficiency", "isovaleryl coA dehydrogenase deficiency", "isovaleryl-CoA dehydrogenase deficiency", "Isovaleryl-CoA dehydrogenase deficiency", "Isovaleric acid CoA dehydrogenase deficiency", "isovaleric acid Coa dehydrogenase deficiency", "Isovaleric acid-CoA dehydrogenase deficiency", "isovaleric acid CoA dehydrogenase deficiency", "Isovaleric Acid-CoA Dehydrogenase Deficiency", "ISOVALERIC ACID CoA DEHYDROGENASE DEFICIENCY", "Isovaleryl-coenzyme A dehydrogenase deficiency", "Isovaleryl-coenzyme A dehydrogenase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isovaleric acidemia", "shortest_name_length": 3}
{"curie": "MONDO:0003950", "names": ["Nipple Cancer", "nipple cancer", "nipple carcinoma", "Nipple Carcinoma", "carcinoma of nipple"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nipple carcinoma", "shortest_name_length": 13}
{"curie": "MONDO:0018092", "names": ["Harada", "VKH disease", "VK syndrome", "vkh syndrome", "VKH syndrome", "VKH Syndrome", "Syndrome, VKH", "Vogt's disease", "harada disease", "Harada disease", "disease haradas", "Harada's disease", "harada's disease", "Harada's syndrome", "harada's syndrome", "VOGT-KOYANAGI SYNDROME", "Vogt-koyanagi syndrome", "Uveomenigitic syndrome", "Uveocutaneous syndrome", "Vogt-Koyanagi syndrome", "uveomeningoencephalitis", "Uveomeningoencephalitis", "Oculocutaneous syndrome", "Uveodermatologic syndrome", "Uveomeningoencephalitides", "UVEO-OTO-CUTANEOUS SYNDROME", "Vogt Koyanagi Harada Disease", "vogt-koyanagi-harada disease", "Vogt-Koyanagi-Harada Disease", "Harada's disease (diagnosis)", "Vogt-Koyanagi-Harada disease", "vogt-koyanagi-harada syndrome", "vogt koyanagi harada syndrome", "Vogt-Koyanagi-Harada Syndrome", "Vogt-Koyanagi-Harada syndrome", "Vogt Koyanagi Harada Syndrome", "Disease, Vogt-Koyanagi-Harada", "Uveomeningoencephalic syndrome", "Syndrome, Vogt-Koyanagi-Harada", "Syndrome, Vogt Koyanagi Harada", "uveomeningoencephalitic syndrome", "Uveomeningoencephalitic Syndrome", "Syndrome, Uveomeningoencephalitic", "Vogt-Koyanagi syndrome (diagnosis)", "VKH - Vogt-Koyanagi-Harada syndrome", "VKH Syndrome (Vogt Koyanagi Harada)", "VKH (Vogt Koyanagi Harada) Syndrome", "Syndrome, VKH (Vogt Koyanagi Harada)", "Vogt-Koyanagi-Harada disease (disorder)", "Vogt-Koyanagi-Harada syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vogt-Koyanagi-Harada disease", "shortest_name_length": 6}
{"curie": "MONDO:0012820", "names": ["CRCS3", "SMAD7 colorectal cancer", "susceptibility to colorectal cancer 3", "COLORECTAL CANCER, SUSCEPTIBILITY TO, 3", "colorectal cancer, susceptibility to, 3", "colorectal cancer, susceptibility to, type 3", "colorectal cancer caused by mutation in SMAD7", "colorectal cancer, susceptibility to, on chromosome 18", "COLORECTAL CANCER, SUSCEPTIBILITY TO, ON CHROMOSOME 18"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorectal cancer, susceptibility to, 3", "shortest_name_length": 5}
{"curie": "UMLS:C4727401", "names": ["Recurrent Thyroid Gland Papillary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Thyroid Gland Papillary Carcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0021375", "names": ["Duodenal Tumor", "duodenum tumor", "duodenal tumor", "Duodenal Neoplasm", "tumor of duodenum", "duodenal neoplasm", "duodenum neoplasm", "Tumor of Duodenum", "Neoplasm of Duodenum", "neoplasm of duodenum", "tumor of the duodenum", "Tumor of the Duodenum", "neoplasm of the duodenum", "Neoplasm of the Duodenum", "duodenum neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tumor of duodenum", "shortest_name_length": 14}
{"curie": "MONDO:0016906", "names": ["del(7q)", "deletion 7q", "7q deletion", "monosomy 7q", "7q monosomy", "partial monosomy 7q", "loss of chromosome 7q", "partial monosomy of chromosome 7q", "partial deletion of chromosome 7q", "partial monosomy of the long arm of chromosome 7", "partial deletion of the long arm of chromosome 7", "partial deletion of the long arm of chromosome type 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of the long arm of chromosome 7", "shortest_name_length": 7}
{"curie": "UMLS:C2828100", "names": ["stage IIIB vulvar cancer", "Stage IIIB Vulvar Cancer", "Stage IIIB Vulvar Carcinoma", "stage IIIB vulvar carcinoma", "Stage IIIB Vulvar Cancer AJCC v7", "stage IIIB vulvar cancer AJCC v7", "Stage IIIB Vulvar Carcinoma AJCC v7", "stage IIIB vulvar carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Vulvar Cancer AJCC v7", "shortest_name_length": 24}
{"curie": "UMLS:C4521784", "names": ["IA", "Stage IA Gastric (Stomach) Cancer", "Pathologic Stage IA Gastric Cancer AJCC v8", "Pathologic Stage IA Gastric Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IA Gastric Cancer AJCC v8", "shortest_name_length": 2}
{"curie": "MONDO:0019559", "names": ["hypertrophic or verrucous lupus erythematosus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophic or verrucous lupus erythematosus", "shortest_name_length": 45}
{"curie": "MONDO:0021443", "names": ["benign lymph node tumor", "Benign Lymph Node Tumor", "benign tumor of lymph node", "benign lymph node neoplasm", "Benign Tumor of Lymph Node", "Benign Lymph Node Neoplasm", "lymph node benign neoplasm", "Benign lymph node neoplasm", "Benign Neoplasm of Lymph Node", "benign neoplasm of lymph node", "Benign neoplasm of lymph node", "benign tumor of the lymph node", "Benign neoplasm of lymph nodes", "benign neoplasm of lymph nodes", "Benign Tumor of the Lymph Node", "Benign Lymph Node Neoplasm NOS", "Benign lymph node neoplasm NOS", "Benign Neoplasm of the Lymph Node", "benign neoplasm of the lymph node", "Benign neoplasm of lymph node, NOS", "Benign neoplasm of lymph node (disorder)", "benign neoplasm of lymph node (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of lymph node", "shortest_name_length": 23}
{"curie": "UMLS:C1333115", "names": ["Colorectal Low-Grade Dysplasia", "Large Intestinal Low Grade Dysplasia", "Colorectal Low Grade Intraepithelial Neoplasia", "Large Intestinal Low Grade Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Low Grade Intraepithelial Neoplasia", "shortest_name_length": 30}
{"curie": "MONDO:0008537", "names": ["Telecanthus", "TELECANTHUS", "telecanthus", "Dystopia canthorum", "eyelids telecanthus", "Telecanthus (finding)", "Syndromic telecanthus", "Corners of eye widely separated", "Increased intercanthal distance", "eyelids telecanthus (physical finding)", "Increased distance between medial canthi"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "telecanthus", "shortest_name_length": 11}
{"curie": "MONDO:0011664", "names": ["IMD41", "CD25 Deficiency", "CD25 DEFICIENCY", "CD25 deficiency", "IL2RA Deficiency", "IL2RA deficiency", "IL2RA DEFICIENCY", "immunodeficiency 41", "immunodeficiency due to CD25 deficiency", "Interleukin 2 Receptor, Alpha, Deficiency of", "INTERLEUKIN 2 RECEPTOR, ALPHA, DEFICIENCY OF", "Interleukin 2 receptor, alpha, deficiency of", "interleukin-2 receptor alpha chain deficiency", "Interleukin-2 receptor alpha chain deficiency", "IMMUNODEFICIENCY 41 WITH LYMPHOPROLIFERATION AND AUTOIMMUNITY", "immunodeficiency 41 with lymphoproliferation and autoimmunity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency due to CD25 deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C1720775", "names": ["tubular necrosis", "Tubular necrosis", "necrosis; tubular", "Tubular necrosis NOS", "Renal Tubule Necrosis", "KIDNEY TUBULE NECROSIS", "RENAL TUBULAR NECROSIS", "renal tubular necrosis", "Renal tubular necrosis", "Kidney tubule necrosis", "Necrosis, Renal Tubule", "Necrosis kidney tubular", "kidney tubular necrosis", "KIDNEY TUBULAR NECROSIS", "Necrosis tubular kidney", "NECROSIS KIDNEY TUBULAR", "NECROSIS TUBULAR KIDNEY", "Kidney tubular necrosis", "kidney; necrosis, tubular", "necrosis; kidney, tubular", "Renal tubular necrosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal tubular necrosis", "shortest_name_length": 16}
{"curie": "MONDO:0016226", "names": ["dysphasia", "Specific Language Disorder", "specific language disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "specific language disorder", "shortest_name_length": 9}
{"curie": "MONDO:0003024", "names": ["BA", "breast angiosarcoma", "Breast angiosarcoma", "Breast Angiosarcoma", "angiosarcoma of breast", "breast hemangiosarcoma", "Angiosarcoma of Breast", "Breast Hemangiosarcoma", "hemangiosarcoma of breast", "Hemangiosarcoma of Breast", "Angiosarcoma of the breast", "angiosarcoma of the breast", "Angiosarcoma of the Breast", "Hemangiosarcoma of the Breast", "hemangiosarcoma of the breast", "breast angiosarcoma (disease)", "angiosarcoma (disease) of breast", "angiosarcoma of breast (diagnosis)", "hemangiosarcoma of breast (diagnosis)", "breast neoplasm malignant sarcoma angiosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast angiosarcoma", "shortest_name_length": 2}
{"curie": "UMLS:C5419752", "names": ["Skin Ewing Sarcoma", "Cutaneous Ewing Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin Ewing Sarcoma", "shortest_name_length": 18}
{"curie": "MONDO:0008008", "names": ["momo syndrome", "MOMO SYNDROME", "MOMO syndrome", "Macrosomia obesity macrocephaly ocular abnormalities", "macrosomia, obesity, macrocephaly, ocular abnormalities", "macrosomia-obesity-macrocephaly-ocular abnormality syndrome", "MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES", "Macrosomia, Obesity, Macrocephaly, And Ocular Abnormalities", "macrosomia, obesity, macrocephaly, and ocular abnormalities", "Macrosomia-obesity-macrocephaly-ocular abnormalities syndrome", "macrosomia-obesity-macrocephaly-ocular abnormalities syndrome", "macrosomia-obesity-macrocephaly-ocular abnormality (MOMO) syndrome", "macrocephaly-obesity-mental disability-ocular abnormalities syndrome", "Macrocephaly-obesity-mental disability-ocular abnormalities syndrome", "Macrocephaly, obesity, mental disability, ocular abnormality syndrome", "macrocephaly, obesity, mental disability, ocular abnormality syndrome", "Macrocrania, obesity, ocular abnormalities (retinal coloboma and nystagmus)", "macrocrania, obesity, ocular abnormalities (retinal coloboma and nystagmus)", "MOMO (macrocephaly, obesity, mental disability, ocular abnormality) syndrome", "Macrocephaly, obesity, mental disability, ocular abnormality syndrome (disorder)", "macrocephaly, obesity, mental disability, ocular abnormality syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MOMO syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0001534", "names": ["eye inflam", "inflamed eye", "Inflamed;eye", "eye inflamed", "EYE INFLAMED", "Eye inflamed", "Bloodshot eye", "HYPEREMIA EYE", "hyperEMIA eye", "Hyperemia eye", "eyes inflamed", "hyperemia eye", "Hyperaemia eye", "hyperemia; eye", "HYPERAEMIA EYE", "eye; hyperemia", "Hyperemia of eye", "ocular hyperemia", "Ocular hyperemia", "OCULAR HYPEREMIA", "Ocular hyperaemia", "ocular hyperaemia", "Hyperemia of eyes", "Hyperaemia of eye", "OCULAR HYPERAEMIA", "Hyperaemia of eyes", "hyperemia of conjunctiva", "Hyperemia of eye (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ocular hyperemia", "shortest_name_length": 10}
{"curie": "MONDO:0044696", "names": ["PEBAS", "encephalopathy, progressive, early-onset, with brain atrophy and spasticity", "ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND SPASTICITY", "early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0001702", "names": ["Labia Majora Cancer", "Labia Majora cancer", "labia majora cancer", "labia majora carcinoma", "Labia Majora Carcinoma", "labium majora carcinoma", "Carcinoma of Labia Majora", "carcinoma of labia majora", "carcinoma of labium majora", "Carcinoma of the Labia Majora", "carcinoma of the labia majora"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "labia majora carcinoma", "shortest_name_length": 19}
{"curie": "UMLS:C4551535", "names": ["Stage IA Cervical Cancer", "Cervical Cancer Stage IA", "AJCC Stage IA Cervical Cancer", "FIGO Stage IA Cervix Carcinoma", "Stage IA Cervical Cancer AJCC v6", "FIGO Stage IA Cervical Carcinoma", "Stage IA Cervical Cancer AJCC v7", "FIGO Stage IA Carcinoma of Cervix", "FIGO Stage IA Cervix Uteri Carcinoma", "FIGO Stage IA Carcinoma of the Cervix", "FIGO Stage IA Uterine Cervix Carcinoma", "FIGO Stage IA Carcinoma of Cervix Uteri", "Stage IA Cervical Cancer AJCC v6 and v7", "FIGO Stage IA Carcinoma of Uterine Cervix", "FIGO Stage IA Carcinoma of the Cervix Uteri", "FIGO Stage IA Carcinoma of the Uterine Cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Cervical Cancer AJCC v6 and v7", "shortest_name_length": 24}
{"curie": "MONDO:0016496", "names": ["PCB variant of GBS", "pharyngeal-cervical-brachial weakness", "PCB variant of Guillain-Barré syndrome", "PCB variant of Guillain-BarrC) syndrome", "pharyngo-cervico-brachial variant of GBS", "pharyngo-cervico-brachial variant of Guillain-Barré syndrome", "pharyngo-cervico-brachial variant of Guillain-BarrC) syndrome", "pharyngeal-cervical-brachial variant of Guillain-Barre syndrome", "pharyngeal-cervical-brachial variant of Guillain-Barré syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pharyngeal-cervical-brachial variant of Guillain-Barre syndrome", "shortest_name_length": 18}
{"curie": "MONDO:0015620", "names": ["syndromic urogenital tract malformation", "syndrome associated with urogenital tract malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic urogenital tract malformation", "shortest_name_length": 39}
{"curie": "MONDO:0004152", "names": ["CLL/SLL with IGVH SHM", "Postgerminal Center Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma", "postgerminal center chronic lymphocytic leukemia/small lymphocytic lymphoma", "Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma with Immunoglobulin Heavy Chain Variable-Region Gene Somatic Hypermutation", "chronic lymphocytic leukemia/small lymphocytic lymphoma with immunoglobulin heavy chain variable-region gene somatic hypermutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic lymphocytic leukemia/small lymphocytic lymphoma with immunoglobulin heavy chain variable-region gene somatic hypermutation", "shortest_name_length": 21}
{"curie": "UMLS:C0740339", "names": ["throat cancer", "Throat Cancer", "Throat cancer", "THROAT CANCER", "Carcinoma;throat", "Throat Carcinoma", "throat carcinoma", "Throat cancer NOS", "carcinoma of the throat"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Throat cancer", "shortest_name_length": 13}
{"curie": "MONDO:0006625", "names": ["hypobaropathy", "Hypobaropathy", "Andes disease", "Altitude anoxia", "alpine sickness", "Alpine sickness", "ANOXIA, ALTITUDE", "ALTITUDE SICKNESS", "Mountain Sickness", "Altitude Sickness", "altitude sickness", "Mountain sickness", "mountain sickness", "Altitude sickness", "Sickness, Altitude", "Sickness, Mountain", "hypobaric sickness", "altitude effects high", "high altitude effects", "high altitude; effects", "HIGH ALTITUTE SICKNESS", "high altitute sickness", "Adverse effect;altitude", "Effects of high altitude", "effects of high altitude", "effects of; high altitude", "Anoxia due to high altitude", "Effects of high altitude, NOS", "disease (or disorder); alpine", "mountain sickness (diagnosis)", "Anoxia caused by high altitude", "Effects of high altitude (disorder)", "Illnesses due to high altitude effects", "disease (or disorder); mountain sickness", "Anoxia caused by high altitude (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "altitude sickness", "shortest_name_length": 13}
{"curie": "UMLS:C1737329", "names": ["Dysmorphia", "Dysmorphism", "Birth defect", "Dysmorphism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dysmorphism", "shortest_name_length": 10}
{"curie": "MONDO:0100086", "names": ["perinatal disease", "perinatal disorder", "perinatal condition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "perinatal disease", "shortest_name_length": 17}
{"curie": "UMLS:C2931282", "names": ["Skeletal dysplasia, San Diego type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skeletal dysplasia, San Diego type", "shortest_name_length": 34}
{"curie": "MONDO:0032828", "names": ["STAHP", "Sod1 Deficiency, Autosomal Recessive", "SOD1 DEFICIENCY, AUTOSOMAL RECESSIVE", "spastic tetraplegia and axial hypotonia, progressive", "SPASTIC TETRAPLEGIA AND AXIAL HYPOTONIA, PROGRESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic tetraplegia and axial hypotonia, progressive", "shortest_name_length": 5}
{"curie": "MONDO:0000516", "names": ["phalanx chondroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phalanx chondroma", "shortest_name_length": 17}
{"curie": "MONDO:0037938", "names": ["inborn disorder of aspartate family metabolism", "inborn error of aspartate family amino acid metabolic process", "inborn aspartate family amino acid metabolic process disorder", "rare inborn error of aspartate family amino acid metabolic process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of aspartate family metabolism", "shortest_name_length": 46}
{"curie": "MONDO:0009240", "names": ["FIGLUria", "FIGLU-Uria", "Figlu-Uria", "FIGLU-URIA", "FTCD deficiency", "Arakawa syndrome 1", "formiminoglutamicaciduria", "formiminoglutamic acidemia", "formiminoglutamic aciduria", "FORMIMINOGLUTAMIC ACIDURIA", "Formiminoglutamic aciduria", "Formiminoglutamic Aciduria", "FORMIMINOTRANSFERASE DEFICIENCY", "Formiminotransferase Deficiency", "formiminotransferase deficiency", "Formiminoglutamicaciduria (FIGLU-uria)", "Formiminoglutamicaciduria (FIGLU-Uria)", "formiminoglutamicaciduria (FIGLU-uria)", "Formiminotransferase deficiency syndrome", "formiminotransferase deficiency syndrome", "GLUTAMATE FORMIMINOTRANSFERASE DEFICIENCY", "glutamate formiminotransferase deficiency", "Deficiency of glutamate formyltransferase", "Glutamate formiminotransferase deficiency", "formiminotransferase deficiency (diagnosis)", "Deficiency of glutamate formiminotransferase", "Formiminotransferase cyclodeaminase deficiency", "formiminotransferase cyclodeaminase deficiency", "Glutamate formiminotransferase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "formiminoglutamic aciduria", "shortest_name_length": 8}
{"curie": "MONDO:0015341", "names": ["congenital panfollicular nevus", "congenital panfollicular nevus (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital panfollicular nevus", "shortest_name_length": 30}
{"curie": "UMLS:C3831089", "names": ["Class 1b Uveal Melanoma", "Uveal Class 1b Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uveal Class 1b Melanoma", "shortest_name_length": 23}
{"curie": "UMLS:C5237461", "names": ["Refractory Transformed T-cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Transformed T-cell Non-Hodgkin Lymphoma", "shortest_name_length": 50}
{"curie": "UMLS:C3896997", "names": ["Toxic Marrow Injury", "Marrow Toxic Injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Marrow Toxic Injury", "shortest_name_length": 19}
{"curie": "UMLS:C1332472", "names": ["Benign Anterior Tongue Tumor", "Benign Anterior Tongue Neoplasm", "Benign Tumor of Anterior Tongue", "Benign Neoplasm of Anterior Tongue", "Benign Tumor of the Anterior Tongue", "Benign Neoplasm of the Anterior Tongue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Anterior Tongue Neoplasm", "shortest_name_length": 28}
{"curie": "MONDO:0021147", "names": ["disorder of development or morphogenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of development or morphogenesis", "shortest_name_length": 40}
{"curie": "UMLS:C1541446", "names": ["Grade III Lymphomatoid Granulomatosis", "childhood grade III lymphomatoid granulomatosis", "Childhood Grade III Lymphomatoid Granulomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Grade III Lymphomatoid Granulomatosis", "shortest_name_length": 37}
{"curie": "UMLS:C1336397", "names": ["Stage IVC Lip Cancer", "Stage IVC Lip Carcinoma", "Stage IVC Carcinoma of Lip", "Stage IVC Lip Cancer AJCC v7", "Stage IVC Lip Cancer AJCC v6", "Stage IVC Carcinoma of the Lip", "Stage IVC Lip Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Lip Cancer AJCC v6 and v7", "shortest_name_length": 20}
{"curie": "UMLS:C1565886", "names": ["Neonatal Indirect Hyperbilirubinemia", "Hyperbilirubinemia, Neonatal Indirect", "Indirect Hyperbilirubinemia, Neonatal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Indirect Hyperbilirubinemia, Neonatal", "shortest_name_length": 36}
{"curie": "UMLS:C0855059", "names": ["Liposarcoma Metastatic", "Metastatic Liposarcoma", "Liposarcoma metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liposarcoma metastatic", "shortest_name_length": 22}
{"curie": "MONDO:0005489", "names": ["dyslexia", "Dyslexia", "dyslexia (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyslexia", "shortest_name_length": 8}
{"curie": "MONDO:0019429", "names": ["X-linked neurodegenerative syndrome Hamel type", "X-linked neurodegenerative syndrome, Hamel type", "X-linked neurodegenerative syndrome Hamel type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked neurodegenerative syndrome, Hamel type", "shortest_name_length": 46}
{"curie": "MONDO:0005509", "names": ["histiocytoma", "HISTIOCYTOMA", "Histiocytoma", "Histiocytomas", "Histiocytoma, NOS", "Histiocytoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "histiocytoma", "shortest_name_length": 12}
{"curie": "UMLS:C5556795", "names": ["Advanced Vaginal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Vaginal Squamous Cell Carcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0025445", "names": ["Wieacker-Wolff syndrome (spectrum)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wieacker-Wolff syndrome (spectrum)", "shortest_name_length": 34}
{"curie": "MONDO:0032592", "names": ["CMD2C", "Dilated Cardiomyopathy-2C", "dilated cardiomyopathy 2C", "CARDIOMYOPATHY, DILATED, 2C", "cardiomyopathy, dilated, 2c"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiomyopathy, dilated, 2c", "shortest_name_length": 5}
{"curie": "MONDO:0017295", "names": ["glycerol kinase deficiency, juvenile form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycerol kinase deficiency, juvenile form", "shortest_name_length": 41}
{"curie": "MONDO:0009118", "names": ["disseminated sclerosis with narcolepsy", "DISSEMINATED SCLEROSIS WITH NARCOLEPSY", "Disseminated Sclerosis with Narcolepsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disseminated sclerosis with narcolepsy", "shortest_name_length": 38}
{"curie": "MONDO:0004648", "names": ["vascular dementia", "Dementia vascular", "dementia vascular", "Vascular dementia", "Vascular Dementia", "Vascular Dementias", "vascular; dementia", "Dementia, Vascular", "dementia; vascular", "Dementias, Vascular", "multifocal dementia", "Vascular dementia NOS", "Vascular dementia, NOS", "Multi Infarct Dementia", "multi infarct dementia", "VAD - Vascular dementia", "Vascular dementia disorders", "Vascular dementia (disorder)", "vascular dementia (diagnosis)", "Vascular dementia, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vascular dementia", "shortest_name_length": 17}
{"curie": "UMLS:C4683652", "names": ["Graft, Prosthesis, or Flap Failure", "Failure of Graft, Prosthesis, or Flap"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Graft, Prosthesis, or Flap Failure", "shortest_name_length": 34}
{"curie": "MONDO:0012581", "names": ["OI8", "OI, type 8", "OI type VIII", "OI, TYPE VIII", "P3H1 osteogenesis imperfecta", "OI8 Osteogenesis imperfecta 8", "osteogenesis imperfecta type 8", "osteogenesis imperfecta, type 8", "osteogenesis imperfecta type VIII", "OSTEOGENESIS IMPERFECTA, TYPE VIII", "Osteogenesis imperfecta, type VIII", "osteogenesis imperfecta, type VIII", "OI, type 8 Osteogenesis imperfecta, type 8", "OI, type VIII Osteogenesis imperfecta, type VIII", "osteogenesis imperfecta caused by mutation in P3H1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteogenesis imperfecta type 8", "shortest_name_length": 3}
{"curie": "MONDO:0013367", "names": ["LQT2", "LQT2 syndrome", "LQT2/5, DIGENIC", "LQT1/2, DIGENIC", "Long QT Syndrome 2", "LONG QT SYNDROME 2", "Long Qt Syndrome 2", "long QT syndrome 2", "long QT syndrome type 2", "LQT2 syndrome (diagnosis)", "long QT syndrome 1/2, digenic", "LONG QT SYNDROME 1/2, DIGENIC", "LONG QT SYNDROME 2/5, DIGENIC", "long QT syndrome 2/5, digenic", "long QT syndrome 2/3, digenic", "long QT syndrome 2/9, digenic", "LONG QT SYNDROME 1/2, DIGENIC (disorder)", "long QT syndrome 2, acquired, susceptibility to", "Long QT syndrome, acquired, reduced susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "long QT syndrome 2", "shortest_name_length": 4}
{"curie": "MONDO:0020292", "names": ["congenital anomaly of the great arteries", "congenital aorta, aortic arch or pulmonary arteries anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital anomaly of the great arteries", "shortest_name_length": 40}
{"curie": "UMLS:C4745180", "names": ["Adrenal Gland Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adrenal Gland Lymphoma", "shortest_name_length": 22}
{"curie": "MONDO:0010417", "names": ["MICPCH", "MRXSNA", "MICPCH SYNDROME", "MICPCH Syndrome", "Micpch syndrome", "X-linked intellectual disability, Najm type", "mental retardation, X-linked, syndromic, Najm type", "MENTAL RETARDATION, X-LINKED, SYNDROMIC, NAJM TYPE", "microcephaly with pontine and cerebellar hypoplasia", "syndromic X-linked intellectual disability Najm type", "intellectual disability, X-linked, syndromic, Najm type", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, NAJM TYPE", "Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia", "MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA", "mental retardation and microcephaly with PONTINE and cerebellar hypoplasia", "mental retardation and microcephaly with pontine and cerebellar hypoplasia", "X-linked intellectual disability - microcephaly - pontocerebellar hypoplasia", "intellectual disability and microcephaly with PONTINE and cerebellar hypoplasia", "intellectual disability and microcephaly with pontine and cerebellar hypoplasia", "X-linked intellectual disability-microcephaly-pontocerebellar hypoplasia syndrome", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH MICROCEPHALY AND PONTINE AND CEREBELLAR HYPOPLASIA", "intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic X-linked intellectual disability Najm type", "shortest_name_length": 6}
{"curie": "UMLS:C4727682", "names": ["Non-Neoplastic Optic Nerve Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Optic Nerve Disorder", "shortest_name_length": 35}
{"curie": "MONDO:0011564", "names": ["CORD8", "Cone-Rod Dystrophy 8", "CONE-ROD DYSTROPHY 8", "cone-rod dystrophy 8", "cone-rod dystrophy type 8", "CONE-ROD DYSTROPHY 8 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cone-rod dystrophy 8", "shortest_name_length": 5}
{"curie": "MONDO:0024715", "names": ["benign synovioma", "Benign Synovioma", "Benign synovioma", "synovioma, benign", "Synovioma, benign", "SYNOVIOMA, BENIGN", "Benign Synovial Tumor", "benign synovial tumor", "benign synovial neoplasm", "benign synovium neoplasm", "benign tumor of synovium", "Benign Tumor of Synovium", "Benign Synovial Neoplasm", "synovium neoplasm, benign", "Benign Neoplasm of Synovium", "benign neoplasm of synovium", "Benign Tumor of the Synovium", "benign tumor of the synovium", "benign neoplasm of the synovium", "Benign Neoplasm of the Synovium", "Synovioma, benign (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign synovial neoplasm", "shortest_name_length": 16}
{"curie": "MONDO:0003393", "names": ["thymus disease", "disorder thymus", "thymus disorder", "Thymus disorder", "Thymus Disorder", "thymus diseases", "thymus disorders", "Thymus disorders", "disorders thymus", "disease of thymus", "Diseases of thymus", "disorder of thymus", "Disorder of thymus", "Thymus disorder NOS", "thymus gland disease", "THYMUS GLAND DISEASE", "thymus gland disorder", "thymus gland diseases", "disorders gland thymus", "Disease of thymus gland", "disease of thymus gland", "Disorder of thymus, NOS", "Disorder of thymus gland", "Diseases of thymus gland", "disorder of thymus gland", "thymus disease or disorder", "DISEASES OF THE THYMUS GLAND", "thymus disorders (diagnosis)", "Disease of thymus gland, NOS", "disease (or disorder); thymus", "disease or disorder of thymus", "Disease of thymus, unspecified", "Unspecified disease of thymus gland", "Disorder of thymus gland (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thymus gland disorder", "shortest_name_length": 14}
{"curie": "MONDO:0004143", "names": ["psammoma", "Psammoma", "psammomas", "psammomatous meningioma", "meningioma psammomatous", "Psammomatous meningioma", "Psammomatous Meningioma", "psammomatous; meningioma", "Psammomatous Meningiomas", "meningioma; psammomatous", "Meningioma, Psammomatous", "Meningiomas, Psammomatous", "psammomatous meningioma (morphologic abnormality)", "Psammomatous meningioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "psammomatous meningioma", "shortest_name_length": 8}
{"curie": "MONDO:0003746", "names": ["Ciliary Body Spindle Cell Melanoma", "ciliary body spindle cell melanoma", "Spindle Cell Melanoma of Ciliary Body", "spindle cell melanoma of ciliary body", "spindle cell melanoma of the Ciliary body", "spindle cell melanoma of the ciliary body", "Spindle Cell Melanoma of the Ciliary Body"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ciliary body spindle cell melanoma", "shortest_name_length": 34}
{"curie": "MONDO:0004599", "names": ["barbiturate abuse", "Barbiturate abuse", "abuse; barbiturate(s)", "barbiturate(s); abuse", "DRUG ABUSE BARBITURATE", "Barbiturate abuse (disorder)", "barbiturate abuse (diagnosis)", "Sedative, hypnotic or anxiolytic abuse, in remission", "Barbiturate and similarly acting sedative or hypnotic abuse, in remission"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "barbiturate abuse", "shortest_name_length": 17}
{"curie": "MONDO:0024474", "names": ["Epithelial Dysplasia", "epithelial dysplasia", "Epithelial dysplasia", "EPITHELIAL DYSPLASIAS", "epithelial; dysplasia", "dysplasia; epithelial", "Intraepithelial Neoplasm", "intraepithelial neoplasm", "intraepithelial neoplasms", "Neoplasm, Intraepithelial", "intraepithelial neoplasia", "Intraepithelial Neoplasms", "Epithelial dysplasia, NOS", "Intraepithelial Neoplasia", "Neoplasms, Intraepithelial", "Epithelial dysplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intraepithelial neoplasia", "shortest_name_length": 20}
{"curie": "MONDO:0008918", "names": ["CACTD", "CACT deficiency", "CACT Deficiency", "CACT DEFICIENCY", "Cact deficiency", "Carnitine-Acylcarnitine Carrier Deficiency", "Carnitine Acylcarnitine Translocase Deficiency", "carnitine-acylcarnitine translocase deficiency", "CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY", "Carnitine-acylcarnitine translocase deficiency", "Carnitine acylcarnitine translocase deficiency", "CARNITINE-acylcarnitine translocase deficiency", "Carnitine-Acylcarnitine Translocase Deficiency", "Carnitine acylcarnitine translocase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carnitine-acylcarnitine translocase deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0001917", "names": ["chronic pinna perichondritis", "chronic perichondritis of pinna", "Chronic perichondritis of pinna", "chronic perichondritis of auricle", "perichondritis of auricle, chronic", "Chronic perichondritis of pinna (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic perichondritis of pinna", "shortest_name_length": 28}
{"curie": "MONDO:0018752", "names": ["Exertional heat stroke", "heat stroke exertional", "Exertional heat stroke (disorder)", "Exertional heat stroke (diagnosis)", "exercise-induced malignant hyperthermia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exercise-induced malignant hyperthermia", "shortest_name_length": 22}
{"curie": "MONDO:0100105", "names": ["BSVD3", "BRAIN SMALL VESSEL DISEASE 3", "brain small vessel disease 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brain small vessel disease 3", "shortest_name_length": 5}
{"curie": "MONDO:0020416", "names": ["Neuhauser anomaly", "Neuhauser anomaly (disorder)", "Neuhauser anomaly (diagnosis)", "congenital anomaly of circulatory system aortic arch Neuhauser anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neuhauser anomaly", "shortest_name_length": 17}
{"curie": "UMLS:C0431098", "names": ["Malignant melanoma in melanosis", "Malignant melanoma in precancerous melais", "Malignant melanoma in precancerous melanosis", "Malignant Melanoma in Precancerous Melanosis", "Malignant Cutaneous (Skin) Melanoma in Precancerous Melanosis", "Malignant melanoma in precancerous melanosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant melanoma in precancerous melanosis", "shortest_name_length": 31}
{"curie": "MONDO:0014466", "names": ["NLS2", "Neu-Laxova syndrome 2", "NEU-LAXOVA SYNDROME 2", "NEU-Laxova syndrome 2", "PSAT1 Neu-Laxova syndrome", "Neu-Laxova syndrome type 2", "Neu-Laxova syndrome caused by mutation in PSAT1", "phosphoserine aminotransferase deficiency, prenatal form", "Neu-Laxova syndrome due to phosphoserine aminotransferase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neu-Laxova syndrome 2", "shortest_name_length": 4}
{"curie": "MONDO:0003663", "names": ["Broad Ligament Endometrioid Adenocarcinoma", "uterine ligament endometrioid adenocarcinoma", "endometrioid adenocarcinoma of uterine ligament"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine ligament endometrioid adenocarcinoma", "shortest_name_length": 42}
{"curie": "UMLS:C3711531", "names": ["Hdl Deficiency, Type 2", "Low Serum Hdl Cholesterol", "Primary hypoalphalipoproteinemia", "Primary hypoalphalipoproteinaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hdl Deficiency, Type 2", "shortest_name_length": 22}
{"curie": "UMLS:C2828183", "names": ["Stage IA Gestational Trophoblastic Tumor", "Stage IA Gestational Trophoblastic Tumor AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Gestational Trophoblastic Tumor AJCC v7", "shortest_name_length": 40}
{"curie": "MONDO:0004017", "names": ["Atypical Pineal Teratoma", "Atypical Pineal teratoma", "atypical pineal teratoma", "Pineal Area Immature Teratoma", "pineal area immature teratoma", "Pineal Region Immature Teratoma", "pineal region immature teratoma", "immature teratoma of pineal area", "Immature Teratoma of Pineal Area", "immature teratoma of pineal region", "Immature Teratoma of Pineal Region", "immature teratoma of the pineal area", "Immature Teratoma of the Pineal Area", "Immature Teratoma of the Pineal Region", "immature teratoma of the pineal region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pineal region immature teratoma", "shortest_name_length": 24}
{"curie": "MONDO:0012550", "names": ["iris pattern", "IRIS PATTERN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "iris pattern", "shortest_name_length": 12}
{"curie": "MONDO:0024473", "names": ["Astrakhan spotted fever"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Astrakhan spotted fever", "shortest_name_length": 23}
{"curie": "UMLS:C5557584", "names": ["Placental Site Nodule Occurring in the Fallopian Tube", "Placental Site Nodule and Plaque Occurring in the Fallopian Tube"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Placental Site Nodule and Plaque Occurring in the Fallopian Tube", "shortest_name_length": 53}
{"curie": "MONDO:0014305", "names": ["SPG63", "spastic paraplegia 63", "hereditary spastic paraplegia 63", "hereditary spastic paraplegia type 63", "autosomal recessive spastic paraplegia 63", "SPASTIC PARAPLEGIA 63, AUTOSOMAL RECESSIVE", "spastic paraplegia 63, autosomal recessive", "Autosomal recessive spastic paraplegia type 63", "autosomal recessive spastic paraplegia type 63", "AMPD2 autosomal recessive complex spastic paraplegia", "familial spastic paraplegia autosomal recessive type 63", "Autosomal recessive spastic paraplegia type 63 (disorder)", "Autosomal recessive spastic paraplegia type 63 (diagnosis)", "autosomal recessive complex spastic paraplegia caused by mutation in AMPD2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 63", "shortest_name_length": 5}
{"curie": "MONDO:0002790", "names": ["seminal vesicle tumor", "seminal vesicle tumour", "tumor of seminal vesicle", "Tumor of seminal vesicle", "Seminal Vesicle neoplasm", "Seminal Vesicle Neoplasm", "seminal vesicle neoplasm", "tumour of seminal vesicle", "Tumour of seminal vesicle", "neoplasm of seminal vesicle", "seminal vesicle neoplasm (disease)", "Tumor of seminal vesicle (disorder)", "neoplasm of seminal vesicle (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "seminal vesicle tumor", "shortest_name_length": 21}
{"curie": "UMLS:C5239192", "names": ["Pre-treatment Disease Complication", "Pre-Treatment Disease Complications"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pre-treatment Disease Complication", "shortest_name_length": 34}
{"curie": "MONDO:0013851", "names": ["BMFS1", "bone marrow failure syndrome 1", "BONE MARROW FAILURE SYNDROME 1", "bone marrow failure syndrome type 1", "autosomal dominant aplasia and myelodysplasia", "autosomal dominant aplastic anemia and myelodysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant aplasia and myelodysplasia", "shortest_name_length": 5}
{"curie": "MONDO:0022611", "names": ["Brunoni syndrome", "Mesomelia, radial hypoplasia bifid thumb unusual facies", "mesomelia, radial hypoplasia bifid thumb unusual facies", "Mesomelic dwarfism, skeletal abnormalities, and ectodermal dysplasia", "mesomelic dwarfism, skeletal abnormalities, and ectodermal dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brunoni syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0008726", "names": ["ABS1", "Ambiguous genitalia-disordered steroidogenesis Antley-Bixler syndrome", "Antley-Bixler syndrome with genital anomaly and disorder of steroidogenesis", "Antley-Bixler Syndrome with Genital Anomalies and Disordered Steroidogenesis", "ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS", "Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis", "shortest_name_length": 4}
{"curie": "MONDO:0010659", "names": ["FRAXE", "MRX109", "XLID109", "FRAXE syndrome", "FRAXE Syndrome", "FRAXE Syndromes", "Syndrome, FRAXE", "FRAXE (disorder)", "Syndromes, FRAXE", "Mar (X) Syndrome", "Fragile XE syndrome", "fragile XE syndrome", "fragile site, folic acid type", "FRAXE intellectual disability", "fragile site on chromosome Xq28", "MENTAL RETARDATION, X-LINKED 109", "FRAXE MENTAL RETARDATION SYNDROME", "fragile site mental retardation 2", "FRAXE mental retardation syndrome", "FRAXE intellectual disability syndrome", "Fragile X-F Mental Retardation Syndrome", "fragile site mental retardation 2 (FMR2)", "X-linked intellectual developmental disorder 109", "FRAXE intellectual disability syndrome (disorder)", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 109", "FRAXE intellectual disability syndrome (diagnosis)", "X-linked mental retardation-fragile site syndrome 2", "Intellectual disability associated with fragile site FRAXE", "intellectual disability associated with fragile site FRAXE", "X-linked mental retardation-fragile site syndrome 2 (FRAXE2)", "X-linked mental retardation associated with fragile site FRAXE", "Mental Retardation, X-Linked, Associated With Fragile Site Fraxe", "MENTAL RETARDATION, X-LINKED, ASSOCIATED WITH FRAGILE SITE FRAXE", "mental retardation, X-linked, associated with fragile site FRAXE", "X-linked intellectual disability associated with fragile site FRAXE", "intellectual disability, X-linked, associated with fragile site FRAXE", "intellectual developmental disorder, X-linked 109, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FRAXE intellectual disability", "shortest_name_length": 5}
{"curie": "UMLS:C1334583", "names": ["Malignant Extraskeletal Cartilaginous and Osseous Tumor", "Malignant Extraskeletal Cartilaginous and Osseous Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Extraskeletal Cartilaginous and Osseous Neoplasm", "shortest_name_length": 55}
{"curie": "UMLS:C1334011", "names": ["High Grade Cervical Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Cervical Intraepithelial Neoplasia", "shortest_name_length": 45}
{"curie": "UMLS:C0750166", "names": ["Venous reflux disorder", "VENOUS DISEASE PERIPHERAL", "Peripheral venous disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peripheral venous disease", "shortest_name_length": 22}
{"curie": "UMLS:C0752164", "names": ["Intracerebral Cavernous Hemangioma", "Hemangioma, Intracerebral Cavernous", "Intracerebral Cavernous Hemangiomas", "Cavernous Hemangioma, Intracerebral", "Hemangiomas, Intracerebral Cavernous", "Cavernous Hemangiomas, Intracerebral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cavernous Hemangioma, Intracerebral", "shortest_name_length": 34}
{"curie": "MONDO:0009620", "names": ["Say-Barber-Miller syndrome", "Say Barber Miller syndrome", "microcephaly hypogammaglobulinemia abnormal immunity", "Microcephaly hypogammaglobulinemia abnormal immunity", "Microcephaly-hypogammaglobulinemia-abnormal immunity syndrome", "microcephaly-hypogammaglobulinemia-abnormal immunity syndrome", "Microcephaly, hypogammaglobulinemia, abnormal immunity syndrome", "Microcephaly, hypogammaglobulinaemia, abnormal immunity syndrome", "MICROCEPHALY WITH CHEMOTACTIC DEFECT AND TRANSIENT HYPOGAMMAGLOBULINEMIA", "Microcephaly with Chemotactic Defect and Transient Hypogammaglobulinemia", "microcephaly with chemotactic defect and transient hypogammaglobulinemia", "Microcephaly, hypogammaglobulinemia, abnormal immunity syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Say-Barber-Miller syndrome", "shortest_name_length": 26}
{"curie": "UMLS:C5419427", "names": ["Unanticipated Adverse Device Effect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unanticipated Adverse Device Effect", "shortest_name_length": 35}
{"curie": "MONDO:0020541", "names": ["GTCT", "GCT of the ovary", "granulosa cell cancer", "cancer of granulosa cell", "granulosa theca cell tumor", "granulosa cell malignant tumor", "malignant granulosa cell neoplasm", "adult ovarian granulosa cell tumor", "Malignant Ovarian Granulosa Cell Tumor", "Malignant ovarian granulosa cell tumor", "ovarian granulosa cell tumor of adults", "maligant granulosa cell tumor of ovary", "malignant ovarian granulosa cell tumor", "adult granulosa cell tumor of the ovary", "Malignant Granulosa Cell Tumor of Ovary", "Malignant ovarian granulosa cell tumour", "granulosa theca cell tumor of the ovary", "Malignant granulosa cell tumor of ovary", "malignant granulosa cell tumor of ovary", "Malignant granulosa cell tumour of ovary", "malignant ovarian granulosa cell neoplasm", "Malignant Ovarian Granulosa Cell Neoplasm", "ovarian neoplasm malignant granulosa cell", "malignant granulosa cell neoplasm of ovary", "Malignant Granulosa Cell Neoplasm of Ovary", "Maligant granulosa cell tumor of the ovary", "malignant granulosa cell tumor of the ovary", "Malignant Granulosa Cell Tumor of the Ovary", "malignant granulosa cell neoplasm of the ovary", "Malignant Granulosa Cell Neoplasm of the Ovary", "malignant granulosa cell tumor of ovary (diagnosis)", "Malignant granulosa cell tumour of ovary (disorder)", "malignant granulosa cell neoplasm of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maligant granulosa cell tumor of ovary", "shortest_name_length": 4}
{"curie": "MONDO:0030916", "names": ["MRD50", "autosomal dominant mental retardation 50", "mental retardation, autosomal dominant 50", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 50", "autosomal dominant intellectual disability 50", "intellectual disability, autosomal dominant 50", "autosomal dominant intellectual developmental disorder 50", "autosomal dominant intellectual developmental disorder-50 with behavioral abnormalities", "intellectual developmental disorder, autosomal dominant 50, with behavioral abnormalities", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 50", "shortest_name_length": 5}
{"curie": "MONDO:0015608", "names": ["AML and myelodysplastic syndromes related to radiation", "acute myeloid leukemia and myelodysplastic syndromes related to radiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia and myelodysplastic syndromes related to radiation", "shortest_name_length": 54}
{"curie": "UMLS:C5447548", "names": ["Refractory Renal Pelvis Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Renal Pelvis Urothelial Carcinoma", "shortest_name_length": 44}
{"curie": "UMLS:C0853852", "names": ["Cystitis E. coli", "Cystitis escherichia", "Escherichial cystitis", "Escherichia coli cystitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cystitis escherichia", "shortest_name_length": 16}
{"curie": "MONDO:0017207", "names": ["Lymphoma by Site", "primary organ-specific lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary organ-specific lymphoma", "shortest_name_length": 16}
{"curie": "MONDO:0000550", "names": ["extra-adrenal Chromaffinoma", "Extra-Adrenal Chromaffinoma", "Extraadrenal Pheochromocytoma", "Extraadrenal pheochromocytoma", "extraadrenal pheochromocytoma", "extra-adrenal pheochromocytoma", "extra adrenal pheochromocytoma", "Extra-Adrenal Pheochromocytoma", "Pheochromocytoma, extraadrenal", "Pheochromocytoma, Extra-Adrenal", "Extra-Adrenal Pheochromocytomas", "Pheochromocytomas, extraadrenal", "Pheochromocytoma, Extra Adrenal", "Pheochromocytomas, Extra-Adrenal", "Extra-Adrenal Chromaffin Neoplasm", "extra-adrenal chromaffin neoplasm", "Extra-Adrenal Sympathetic Paraganglioma", "extra-adrenal sympathetic paraganglioma", "Extra-Adrenal Sympathetic Paraganglionic Neoplasm", "extra-adrenal sympathetic Paraganglionic neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extra-adrenal sympathetic paraganglioma", "shortest_name_length": 27}
{"curie": "UMLS:C2608080", "names": ["Renal Hypoplasia, Isolated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal Hypoplasia, Isolated", "shortest_name_length": 26}
{"curie": "MONDO:0003326", "names": ["GNB-i", "Intermixed ganglioneuroblastoma", "Ganglioneuroblastoma, Intermixed", "ganglioneuroblastoma, intermixed", "Ganglioneuroblastoma, intermixed", "intermixed schwannian stroma-rich ganglioneuroblastoma", "Ganglioneuroblastoma, Intermixed (Schwannian Stroma-Rich)", "Intermixed ganglioneuroblastoma (morphologic abnormality)", "ganglioneuroblastoma, intermixed (Schwannian Stroma-rich)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intermixed schwannian stroma-rich ganglioneuroblastoma", "shortest_name_length": 5}
{"curie": "MONDO:0005753", "names": ["epiglottitis", "Epiglottitis", "EPIGLOTTITIS", "Epiglottitides", "Supraglottitis", "supraglottitis", "Epiglottitis NOS", "Epiglottitis, NOS", "acute epiglottitis", "Epiglottitis (disorder)", "epiglottitis (diagnosis)", "mucosa of epiglottis inflammation", "inflammation of mucosa of epiglottis", "acute epiglottitis and supraglottitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epiglottitis", "shortest_name_length": 12}
{"curie": "UMLS:C1960540", "names": ["Placental Aromatase Deficiency", "Placental aromatase deficiency", "placental disorders deficiency aromatase", "Placental aromatase deficiency (disorder)", "Placental aromatase deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Placental aromatase deficiency", "shortest_name_length": 30}
{"curie": "UMLS:C0280180", "names": ["relapsed adult NHL, low grade", "low-grade, relapsed adult NHL", "adult NHL, relapsed, low grade", "recurrent adult NHL, low grade", "NHL, low grade, relapsed adult", "low-grade, recurrent adult NHL", "adult NHL, recurrent, low grade", "NHL, low grade, recurrent adult", "Recurrent Low Grade Adult Non-Hodgkin's Lymphoma", "relapsed adult non-Hodgkin's lymphoma, low grade", "low-grade, relapsed adult non-Hodgkin's lymphoma", "adult non-Hodgkin's lymphoma, low grade, relapsed", "non-Hodgkin's lymphoma, low grade, relapsed adult", "recurrent adult non-Hodgkin's lymphoma, low grade", "adult non-Hodgkin's lymphoma, low grade, recurrent", "non-Hodgkin's lymphoma, low grade, recurrent adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Low Grade Adult Non-Hodgkin's Lymphoma", "shortest_name_length": 29}
{"curie": "UMLS:C1336281", "names": ["Stage II Ampullary Carcinoma", "Stage II Ampulla of Vater Cancer", "Ampulla of Vater Cancer Stage II", "Stage II Ampulla of Vater Carcinoma", "Stage II Ampulla of Vater Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Ampulla of Vater Cancer AJCC v7", "shortest_name_length": 28}
{"curie": "UMLS:C0279838", "names": ["oropharynx cancer, recurrent", "relapsed cancer of oropharynx", "relapsed oropharynx carcinoma", "Relapsed Oropharynx Carcinoma", "Relapsed Cancer of Oropharynx", "Relapsed Oropharyngeal Cancer", "relapsed oropharyngeal cancer", "recurrent oropharyngeal cancer", "Recurrent Oropharyngeal Cancer", "recurrent oropharynx carcinoma", "Recurrent Oropharynx Carcinoma", "Recurrent Cancer of Oropharynx", "recurrent cancer of oropharynx", "Oropharyngeal cancer recurrent", "oropharyngeal cancer, recurrent", "Oropharyngeal Cancer, Recurrent", "relapsed oropharyngeal carcinoma", "Relapsed Oropharyngeal Carcinoma", "relapsed carcinoma of oropharynx", "Relapsed Carcinoma of Oropharynx", "Relapsed Cancer of the Oropharynx", "relapsed cancer of the oropharynx", "Recurrent Oropharyngeal Carcinoma", "recurrent carcinoma of oropharynx", "Recurrent Carcinoma of Oropharynx", "Recurrent Cancer of the Oropharynx", "recurrent cancer of the oropharynx", "Relapsed Carcinoma of the Oropharynx", "relapsed carcinoma of the oropharynx", "Recurrent Oropharyngeal Throat Cancer", "recurrent carcinoma of the oropharynx", "Recurrent Carcinoma of the Oropharynx"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oropharyngeal cancer recurrent", "shortest_name_length": 28}
{"curie": "MONDO:0013153", "names": ["Ibd28", "IBD28", "INFLAMMATORY BOWEL DISEASE 28", "inflammatory bowel disease 28", "Inflammatory Bowel Disease 28", "IL10RA inflammatory bowel disease", "inflammatory bowel disease type 28", "inflammatory bowel disease 28, autosomal recessive", "INFLAMMATORY BOWEL DISEASE 28, AUTOSOMAL RECESSIVE", "Inflammatory Bowel Disease 28, Autosomal Recessive", "inflammatory bowel disease caused by mutation in IL10RA", "INFLAMMATORY BOWEL DISEASE, EARLY-ONSET, AUTOSOMAL RECESSIVE", "inflammatory bowel disease, early-onset, autosomal recessive", "early onset autosomal recessive inflammatory bowel disease 28", "inflammatory bowel disease 28, early onset, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory bowel disease 28", "shortest_name_length": 5}
{"curie": "MONDO:0017518", "names": ["short toes, bilateral", "brachydactyly of toes, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly of toes, bilateral", "shortest_name_length": 21}
{"curie": "UMLS:C3272484", "names": ["Ampulla of Vater Somatostatin Producing NET", "Ampulla of Vater Somatostatin Producing Neuroendocrine Tumor", "Ampulla of Vater Somatostatin-Producing Neuroendocrine Tumor", "Somatostatin Producing Neuroendocrine Tumor of the Ampullary Region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ampulla of Vater Somatostatin-Producing Neuroendocrine Tumor", "shortest_name_length": 43}
{"curie": "UMLS:C4683426", "names": ["II 55 Years and Older", "Stage II Thyroid Gland Papillary Cancer 55 Years and Older", "Stage II Thyroid Gland Papillary Carcinoma 55 Years and Older AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Thyroid Gland Papillary Carcinoma 55 Years and Older AJCC v8", "shortest_name_length": 21}
{"curie": "MONDO:0020545", "names": ["staphylococcal TSS", "Staphylococcal TSS", "Toxic shock syndrome", "Staphylococcal scarlet fever", "STAPHYLOCOCCAL SCARLET FEVER", "Staphylococcal toxic-shock syndrome", "staphylococcal toxic-shock syndrome", "Staphylococcal toxic shock syndrome", "Staphylococcus toxic shock syndrome", "Toxic shock syndrome staphylococcal", "toxic shock syndrome staphylococcal", "Staphylococcus caused toxic shock syndrome", "Staphylococcal toxic shock syndrome (disorder)", "Staphylococcal toxic shock syndrome (diagnosis)", "STAPHYLOCOCCAL SCARLET FEVER TOXIC SHOCK SYNDROME", "STAPHYLOCOCCAL SCARLET FEVER <TOXIC SHOCK SYNDROME>"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "staphylococcal toxic-shock syndrome", "shortest_name_length": 18}
{"curie": "MONDO:0013544", "names": ["ATFB11", "atrial fibrillation familial 11", "GJA5 familial atrial fibrillation", "atrial fibrillation, familial, 11", "ATRIAL FIBRILLATION, FAMILIAL, 11", "atrial fibrillation, familial, type 11", "atrial fibrillation familial 11 (diagnosis)", "familial atrial fibrillation caused by mutation in GJA5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial fibrillation, familial, 11", "shortest_name_length": 6}
{"curie": "MONDO:0011976", "names": ["Rajab-Spranger syndrome", "Rajab Spranger syndrome", "Lipodystrophy-intellectual disability-deafness syndrome", "lipodystrophy-intellectual disability-deafness syndrome", "Lipodystrophy, intellectual disability, deafness syndrome", "lipodystrophy, intellectual disability, deafness syndrome", "Lipodystrophy-intellectual disability-hearing loss syndrome", "Lipodystrophy, intellectual disability, deafness syndrome (disorder)", "lipodystrophy, intellectual disability, deafness syndrome (diagnosis)", "LIPODYSTROPHY, GENERALIZED, WITH MENTAL RETARDATION, DEAFNESS, SHORT STATURE, AND SLENDER BONES", "Lipodystrophy, Generalized, with Mental Retardation, Deafness, Short Stature, and Slender Bones", "lipodystrophy, generalized, with mental retardation, deafness, short stature, and slender bones", "lipodystrophy, generalized, with intellectual disability, deafness, short stature, and slender bones"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lipodystrophy-intellectual disability-deafness syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0003523", "names": ["gastrinoma", "Gastrinoma", "G-cell tumor", "G-Cell Tumor", "G Cell Tumor", "G cell tumor", "Gastrin cell tumour", "gastrin cell tumour", "malignant gastrinoma", "Gastrin-Producing NET", "gastrin-producing NET", "Gastrin Secreting Tumor", "Gastrin Secreting tumor", "gastrin secreting tumor", "G-cell gastrin producing tumor", "G-Cell Gastrin Producing Tumor", "Gastrin-Producing Neuroendocrine Tumor", "gastrin-producing neuroendocrine tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastrin-producing neuroendocrine tumor", "shortest_name_length": 10}
{"curie": "MONDO:0019213", "names": ["cerebral organic aciduria", "brain inherited organic acidemia", "inherited organic acidemia of brain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral organic aciduria", "shortest_name_length": 25}
{"curie": "UMLS:C3897526", "names": ["Stage IIIC Primary Peritoneal Cancer", "Stage IIIC Primary Peritoneal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Primary Peritoneal Cancer AJCC v7", "shortest_name_length": 36}
{"curie": "MONDO:0014317", "names": ["BMFS2", "BONE MARROW FAILURE SYNDROME 2", "bone marrow failure syndrome 2", "bone marrow failure syndrome type 2", "pancytopenia-developmental delay syndrome", "Trilineage bone marrow failure-developmental delay syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancytopenia-developmental delay syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C5206722", "names": ["Advanced Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Squamous Cell Carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0035668", "names": ["isolated optic neuritis with anti-MOG antibodies", "Isolated optic neuritis with anti-myelin oligodendrocyte glycoprotein antibodies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated optic neuritis with anti-MOG antibodies", "shortest_name_length": 48}
{"curie": "MONDO:0007247", "names": ["IBGC childhood onset", "IBGC, childhood onset", "IBGC, childhood-onset", "IBGC, CHILDHOOD-ONSET", "idiopathic basal ganglia calcification childhood-onset", "Idiopathic basal ganglia calcification, childhood onset", "Basal Ganglia Calcification, Idiopathic, Childhood-Onset", "basal ganglia calcification, idiopathic, childhood-onset", "BASAL GANGLIA CALCIFICATION, IDIOPATHIC, CHILDHOOD-ONSET", "bilateral striopallidodentate calcinosis childhood-onset", "Bilateral striopallidodentate calcinosis, childhood onset", "striopallidodentate calcinosis, bilateral, childhood-onset", "Striopallidodentate Calcinosis, Bilateral, Childhood-Onset", "STRIOPALLIDODENTATE CALCINOSIS, BILATERAL, CHILDHOOD-ONSET", "cerebral calcification nonarteriosclerotic idiopathic childhood-onset", "Cerebral Calcification, Nonarteriosclerotic, Idiopathic, Childhood-Onset", "Cerebral calcification, nonarteriosclerotic, childhood onset, idiopathic", "CEREBRAL CALCIFICATION, NONARTERIOSCLEROTIC, IDIOPATHIC, CHILDHOOD-ONSET", "cerebral calcification, nonarteriosclerotic, idiopathic, childhood-onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "basal ganglia calcification, idiopathic, childhood-onset", "shortest_name_length": 20}
{"curie": "UMLS:C4743665", "names": ["Advanced Neuroendocrine Tumor", "Advanced Well Differentiated Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Neuroendocrine Tumor", "shortest_name_length": 29}
{"curie": "UMLS:C4688340", "names": ["Unresectable Malignant Solid Tumor", "Unresectable Malignant Solid Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Malignant Solid Neoplasm", "shortest_name_length": 34}
{"curie": "MONDO:0019617", "names": ["Hypopituitarism due to empty sella turcica syndrome", "hypopituitarism due to empty sella turcica syndrome", "Pituitary deficiency due to empty sella turcica syndrome", "pituitary deficiency due to empty sella turcica syndrome", "Pituitary deficiency due to empty sella turcica syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pituitary deficiency due to empty sella turcica syndrome", "shortest_name_length": 51}
{"curie": "MONDO:0021112", "names": ["Scrotal Ca", "Scrotal cancer", "scrotal cancer", "scrotum cancer", "cancer scrotum", "Cancer of scrotum", "cancer of scrotum", "CA - Cancer of scrotum", "Malignant Scrotal Tumor", "malignant scrotal tumor", "Malignant scrotal tumor", "malignant scrotum tumor", "Malignant scrotal tumour", "malignant scrotal neoplasm", "Malignant Tumor of Scrotum", "Malignant tumor of scrotum", "malignant scrotum neoplasm", "Malignant Scrotal Neoplasm", "malignant tumor of scrotum", "Malignant tumour of scrotum", "Malignant Neoplasm of Scrotum", "Malignant neoplasm of scrotum", "malignant neoplasm of scrotum", "Malignant Tumor of the Scrotum", "malignant tumor of the scrotum", "Malignant Neoplasm of the Scrotum", "malignant neoplasm of the scrotum", "Malignant tumor of scrotum (disorder)", "malignant neoplasm of scrotum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scrotum cancer", "shortest_name_length": 10}
{"curie": "MONDO:0005762", "names": ["Filovirus Infection", "Filovirus infection", "Infection, Filovirus", "Filovirus Infections", "Filoviridae Infection", "Filoviridae Infections", "Infection, Filoviridae", "Infections, Filoviridae", "DISEASES DUE TO FILOVIRUS", "Disease due to Filoviridae", "Disease due to Filovirus, NOS", "Disease caused by Filoviridae", "Filoviridae infectious disease", "Filoviridae disease or disorder", "Filoviridae caused disease or disorder", "Disease caused by Filoviridae (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Filoviridae infectious disease", "shortest_name_length": 19}
{"curie": "UMLS:C4727175", "names": ["Recurrent EBV-Positive Diffuse Large B-Cell Lymphoma, NOS", "Recurrent EBV-Positive Diffuse Large B-Cell Lymphoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent EBV-Positive Diffuse Large B-Cell Lymphoma, Not Otherwise Specified", "shortest_name_length": 57}
{"curie": "MONDO:0003070", "names": ["Axillary Adenitis", "axillary adenitis", "Axillary adenitis", "axillary; adenitis", "adenitis; axillary", "Axillary Lymphadenitis", "Axillary lymphadenitis", "axillary lymphadenitis", "axilla lymphadenitis (disease)", "lymphadenitis (disease) of axilla"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "axillary lymphadenitis", "shortest_name_length": 17}
{"curie": "UMLS:C0748052", "names": ["PSORIASIS EXFOLIATIVE", "Exfoliative psoriasis", "Erythrodermic psoriasis", "psoriasis erythrodermic", "Psoriatic erythrodermia", "erythrodermic psoriasis", "Erythrodermic psoriasis (disorder)", "Exfoliative dermatitis due to psoriasis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Erythrodermic psoriasis", "shortest_name_length": 21}
{"curie": "UMLS:C5420226", "names": ["Benign Oral Cavity Soft Tissue Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Oral Cavity Soft Tissue Neoplasm", "shortest_name_length": 39}
{"curie": "UMLS:C0041784", "names": ["forearm deformity", "forearm; deformity", "deformity; forearm", "Deformity of Forearm", "deformity of forearm", "deformity of forearm (physical finding)", "Unspecified deformity of forearm, excluding fingers"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unspecified deformity of forearm, excluding fingers", "shortest_name_length": 17}
{"curie": "MONDO:0016987", "names": ["Neuroacanthocytosis", "neuroacanthocytosis", "neuroacanthocytosis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuroacanthocytosis", "shortest_name_length": 19}
{"curie": "MONDO:0030059", "names": ["DEE87", "EIEE87", "early infantile epileptic encephalopathy 87", "developmental and epileptic encephalopathy 87", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 87", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 87", "epileptic encephalopathy, early infantile, 87", "developmental and epileptic encephalopathy, 87"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 87", "shortest_name_length": 5}
{"curie": "MONDO:0700069", "names": ["POMGNT2 myopathy", "POMGNT2-related myopathy", "myopathy caused by mutation in POMGNT2", "myopathy caused by variation in POMGNT2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy caused by variation in POMGNT2", "shortest_name_length": 16}
{"curie": "MONDO:0002068", "names": ["female breast lower-inner quadrant cancer", "malignant tumor of lower inner quadrant of female breast", "malignant neoplasm of lower-inner quadrant of female breast", "Malignant neoplasm of lower-inner quadrant of female breast", "malignant neoplasm of lower inner quadrant of female breast", "Malignant neoplasm of lower-inner quadrant of breast, female", "Malignant neoplasm of lower-inner quadrant of female breast (disorder)", "malignant neoplasm of lower inner quadrant of female breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "female breast lower-inner quadrant cancer", "shortest_name_length": 41}
{"curie": "MONDO:0017805", "names": ["intellectual disability-hypotonia-brachycephaly-pyloric stenosis-cryptorchidism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability-hypotonia-brachycephaly-pyloric stenosis-cryptorchidism syndrome", "shortest_name_length": 88}
{"curie": "MONDO:0013638", "names": ["WARBM3", "micro syndrome 3", "Micro Syndrome 3", "MICRO SYNDROME 3", "WARBURG micro syndrome 3", "Warburg micro syndrome 3", "WARBURG MICRO SYNDROME 3", "RAB18 Warburg micro syndrome", "Warburg micro syndrome type 3", "Warburg micro syndrome caused by mutation in RAB18"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Warburg micro syndrome 3", "shortest_name_length": 6}
{"curie": "UMLS:C4682555", "names": ["Stage I Uterine Corpus Leiomyosarcoma", "Stage I Uterine Corpus Leiomyosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Uterine Corpus Leiomyosarcoma AJCC v8", "shortest_name_length": 37}
{"curie": "MONDO:0019679", "names": ["Brachydactyly type A7", "brachydactyly type A7", "Brachydactyly Smorgasbord type", "brachydactyly Smorgasbord type", "Brachydactyly, Smorgasbord type", "brachydactyly, Smorgasbord type", "Brachydactyly type A7 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly type A7", "shortest_name_length": 21}
{"curie": "MONDO:0012197", "names": ["aplastic anemia", "anemia aplastic", "secondary aplastic anemia", "idiopathic aplastic anemia", "Idiopathic aplastic anemia", "Idiopathic Aplastic Anemia", "aplastic anemia idiopathic", "Idiopathic aplastic anaemia", "Aplastic anemia, idiopathic", "idiopathic aplastic aplasia", "Idiopathic Aplastic Aplasia", "anemia; aplastic, idiopathic", "anemia; idiopathic, aplastic", "Idiopathic aplastic anemia,NOS", "Idiopathic bone marrow failure", "idiopathic bone marrow failure", "APLASTIC ANEMIA, SUSCEPTIBILITY TO", "aplastic Anemia, susceptibility to", "Idiopathic aplastic anemia (disorder)", "idiopathic aplastic anemia (diagnosis)", "APLASTIC ANEMIA, SUSCEPTIBILITY TO (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic aplastic anemia", "shortest_name_length": 15}
{"curie": "UMLS:C1696371", "names": ["Tonsillitis bacterial", "bacterial tonsillitis", "Bacterial tonsillitis", "Bacterial tonsillitis (disorder)", "bacterial tonsillitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bacterial tonsillitis", "shortest_name_length": 21}
{"curie": "UMLS:C4524749", "names": ["Postneoadjuvant Therapy Stage IV Gastroesophageal Junction Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postneoadjuvant Therapy Stage IV Gastroesophageal Junction Adenocarcinoma AJCC v8", "shortest_name_length": 81}
{"curie": "MONDO:0019735", "names": ["pmr", "Senile arthritis", "ARTHRITIS, SENILE", "arthritis; senile", "senile; arthritis", "Polymyalgia Rheumatica", "Polymyalgia rheumatica", "polymyalgia rheumatica", "POLYMYALGIA RHEUMATICA", "POLYMYALGIA ARTERITICA", "arteritica; polymyalgia", "polymyalgia; arteritica", "rheumatica; polymyalgia", "polymyalgia; rheumatica", "polymyalgia rheumatica (PMR)", "PMR - Polymyalgia rheumatica", "MYALGIC SYNDROME OF THE AGED", "Forestier-Certonciny syndrome", "Forestier Certonciny Syndrome", "Forestier-Certonciny Syndrome", "Rhizomelic pseudopolyarthritis", "rhizomelic pseudopolyarthritis", "Rhizomelic Pseudopolyarthritis", "Syndrome, Forestier-Certonciny", "Polymyalgia rheumatica syndrome", "Peri-Extra-Articular Rheumatism", "Pseudopolyarthritis, Rhizomelic", "Rheumatism, Peri-Extra-Articular", "Rhizomelic Pseudopolyarthritides", "Rheumatism, Peri Extra Articular", "Polymyalgia rheumatica (disorder)", "Pseudopolyarthritides, Rhizomelic", "polymyalgia rheumatica (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polymyalgia rheumatica", "shortest_name_length": 3}
{"curie": "MONDO:0018772", "names": ["CPD4", "JBTS", "CPD IV", "syndrome joubert", "Joubert syndrome", "Joubert Syndrome", "JOUBERT SYNDROME", "joubert syndrome", "Vermian agenesis", "jouberts syndrome", "pure Joubert syndrome", "Pure Joubert syndrome", "Joubert syndrome type A", "Classic Joubert syndrome", "classic Joubert syndrome", "Cerebellar vermis aplasia", "Cerebellar vermis agenesis", "cerebellar vermis agenesis", "Joubert syndrome (disorder)", "Complete agenesis of vermis", "Joubert-Boltshauser syndrome", "JOUBERT-BOLTSHAUSER SYNDROME", "Joubert syndrome (diagnosis)", "Agenesis of cerebellar vermis", "Agenesis of Cerebellar Vermis", "Cerebello-Oculo-Renal Syndrome", "Familial Aplasia of the Vermis", "Familial aplasia of the vermis", "Cerebelloparenchymal disorder 4", "cerebelloparenchymal disorder IV", "Cerebelloparenchymal Disorder IV", "Cerebelloparenchymal disorder IV", "CEREBELLOPARENCHYMAL DISORDER IV", "Complete agenesis of vermis (disorder)", "Familial aplasia of the vermis (disorder)", "cerebelloparenchymal disorder IV (CPD IV)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0748076", "names": ["psychotic disorder due to general medical condition", "PSYCHOTIC DISORDER DUE TO GENERAL MEDICAL CONDITION", "Psychotic Disorder Due to a General Medical Condition", "Psychotic disorder due to a general medical condition", "Psychotic disorder due to a general medical condition NOS", "psychotic disorder due to general medical condition (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Psychotic disorder due to a general medical condition", "shortest_name_length": 51}
{"curie": "MONDO:0001345", "names": ["Antidepressant type abuse", "antidepressant type abuse"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "antidepressant type abuse", "shortest_name_length": 25}
{"curie": "MONDO:0001746", "names": ["optic disk drusen", "Optic Disc Drusen", "Optic Disk Drusen", "optic disc drusen", "drusen optic disc", "Optic disc drusen", "drusen optic disk", "Optic Nerve Drusen", "Optic Disk Drusens", "drusen optic nerve", "Drusen, Optic Disk", "Optic Disc Drusens", "optic nerve drusen", "drusen nerve optic", "Drusen, Optic Disc", "Optic nerve drusen", "Drusen, Optic Nerve", "Drusen of optic disc", "drusen of optic disc", "optic nerve head drusen", "Optic nerve head drusen", "Hyaline bodies of optic disc", "optic disc drusen (diagnosis)", "Drusen of optic disc (finding)", "drusen were present in the optic disc", "drusen of optic disc (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "optic disk drusen", "shortest_name_length": 17}
{"curie": "MONDO:0007369", "names": ["HCP", "CPO DEFICIENCY", "Cpx deficiency", "CPX DEFICIENCY", "coproporphyria", "CPO deficiency", "Cpo deficiency", "Cpox deficiency", "CPRO deficiency", "CPOX DEFICIENCY", "Harderoporphyria", "porphyria hepatica II", "Porphyria hepatica II", "Berger-Goldberg syndrome", "coproporphyria hereditary", "Hereditary coproporphyria", "COPROPORPHYRIA HEREDITARY", "Hereditary Coproporphyria", "hereditary coproporphyria", "Coproporphyria, Hereditary", "Coproporphyria, hereditary", "COPROPORPHYRIA, HEREDITARY", "coproporphyria, hereditary", "coproporphyria; hereditary", "HCP - Hereditary coproporphyria", "HCP (hereditary coproporphyria)", "hereditary coproporphyria (HCP)", "porphyria hepatica coproporphyria", "hereditary coproporphyria porphyria", "Hereditary coproporphyria (disorder)", "Coproporphyrinogen Oxidase Deficiency", "Coproporphyrinogen oxidase deficiency", "COPROPORPHYRINOGEN OXIDASE DEFICIENCY", "hereditary coproporphyria (diagnosis)", "coproporphyrinogen oxidase deficiency", "Deficiency, Coproporphyrinogen Oxidase", "CPO - Coproporphyrinogen oxidase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary coproporphyria", "shortest_name_length": 3}
{"curie": "UMLS:C0859290", "names": ["black spot", "blacks spot", "black spots", "black spotted", "black spotting"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "black spot", "shortest_name_length": 10}
{"curie": "MONDO:0024499", "names": ["Bone Vascular Tumor", "bone vascular tumor", "bone vascular neoplasm", "vascular bone neoplasm", "Vascular Bone Neoplasm", "vascular tumor of bone", "Bone Vascular Neoplasm", "Vascular Tumor of Bone", "osseous vascular tumor", "Osseous Vascular Tumor", "Osseous Vascular Neoplasm", "osseous vascular neoplasm", "vascular neoplasm of bone", "Vascular Neoplasm of Bone", "Vascular Tumor of the Bone", "vascular tumor of the bone", "vascular neoplasm of the bone", "Vascular Neoplasm of the Bone", "vascular neoplasm of bone (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vascular bone neoplasm", "shortest_name_length": 19}
{"curie": "MONDO:0016676", "names": ["hyperzincemia and hypercalprotectinemia", "recurrent infections-inflammatory syndrome due to zinc metabolism disorder syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "recurrent infections-inflammatory syndrome due to zinc metabolism disorder syndrome", "shortest_name_length": 39}
{"curie": "UMLS:C0264291", "names": ["Pharynx Cyst", "cyst of pharynx", "Cyst of pharynx", "Pharyngeal cyst", "Cyst of Pharynx", "Pharyngeal Cyst", "Cyst of the Pharynx", "Cyst of pharynx (disorder)", "cyst of pharynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cyst of pharynx", "shortest_name_length": 12}
{"curie": "UMLS:C4727414", "names": ["Recurrent Submandibular Gland Mucoepidermoid Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Submandibular Gland Mucoepidermoid Carcinoma", "shortest_name_length": 54}
{"curie": "UMLS:C0887800", "names": ["Psychogenic Inversion of Circadian Rhythm", "Inversion of Circadian Rhythm, Psychogenic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Psychogenic Inversion of Circadian Rhythm", "shortest_name_length": 41}
{"curie": "UMLS:C1336071", "names": ["Splenic Non-Hodgkin Lymphoma", "Splenic Non-Hodgkin's Lymphoma", "Non-Hodgkin Lymphoma of Spleen", "Non-Hodgkin's Lymphoma of Spleen", "non-Hodgkin's lymphoma of spleen", "Non-Hodgkin Lymphoma of the Spleen", "Non-Hodgkin's Lymphoma of the Spleen", "Primary Splenic Non-Hodgkin's Lymphoma", "non-Hodgkin's lymphoma of spleen (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-Hodgkin's lymphoma of spleen", "shortest_name_length": 28}
{"curie": "UMLS:C0271152", "names": ["Glaucoma fulminans", "Malignant glaucoma", "malignant; glaucoma", "glaucoma; malignant", "Glaucoma, malignant", "Ciliary block glaucoma", "Aqueous humor misdirect", "Aqueous humour misdirect", "Ciliary block glaucoma (diagnosis)", "Aqueous humor misdirect (disorder)", "glaucoma following surgery ciliary block"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant glaucoma", "shortest_name_length": 18}
{"curie": "UMLS:C0236106", "names": ["PHOTOSENSITIVITY ALLERGIC REACT", "Photosensitivity allergic reaction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Photosensitivity allergic reaction", "shortest_name_length": 31}
{"curie": "UMLS:C4526654", "names": ["stage IIIA malignant mesothelioma", "Stage IIIA Pleural Malignant Mesothelioma", "stage IIIA pleural malignant mesothelioma AJCC v8", "Stage IIIA Pleural Malignant Mesothelioma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Pleural Malignant Mesothelioma AJCC v8", "shortest_name_length": 33}
{"curie": "MONDO:0018306", "names": ["Giscelli syndrome", "Griscelli disease", "Griscelli syndrome", "Griscelli-Pruniéras syndrome", "Griscelli-Prunieras syndrome", "Chédiak-Higashi-like syndrome", "Griscelli-PruniC)ras syndrome", "Chediak-Higashi-like syndrome", "Griscelli-Pruni��ras syndrome", "ChC)diak-Higashi-like syndrome", "Ch��diak-Higashi-like syndrome", "immunodeficiency; partial albinism", "partial; albinism, immunodeficiency", "albinism; partial, immunodeficiency", "Partial albinism with immunodeficiency", "Griscelli syndrome with immunodeficiency", "hypopigmentation immunodeficiency disease", "Hypopigmentation-immunodeficiency disease", "partial albinism-immunodeficiency syndrome", "Partial albinism-immunodeficiency syndrome", "Hypopigmentation-immunodeficiency disease (disorder)", "hypopigmentation immunodeficiency disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Griscelli syndrome", "shortest_name_length": 17}
{"curie": "UMLS:C0036211", "names": ["Sarcoma 180", "sarcoma 180", "Crocker Sarcoma 180", "Sarcoma 180, Crocker"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sarcoma 180", "shortest_name_length": 11}
{"curie": "MONDO:0004233", "names": ["Pleomorphic rhabdomyosarcoma", "Pleomorphic Rhabdomyosarcoma", "Childhood Anaplastic Rhabdomyosarcoma", "childhood anaplastic Rhabdomyosarcoma", "childhood anaplastic rhabdomyosarcoma", "Childhood Pleomorphic Rhabdomyosarcoma", "pediatric pleomorphic rhabdomyosarcoma", "Pleomorphic Childhood Rhabdomyosarcoma", "pleomorphic pediatric rhabdomyosarcoma", "pleomorphic childhood rhabdomyosarcoma", "childhood pleomorphic rhabdomyosarcoma", "Pediatric Pleomorphic Rhabdomyosarcoma", "pediatric rhabdomyosarcoma, pleomorphic", "rhabdomyosarcoma, pediatric pleomorphic", "rhabdomyosarcoma, pleomorphic childhood", "rhabdomyosarcoma, childhood pleomorphic", "childhood rhabdomyosarcoma, pleomorphic", "pleomorphic rhabdomyosarcoma of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood pleomorphic rhabdomyosarcoma", "shortest_name_length": 28}
{"curie": "MONDO:0007241", "names": ["Familial isolated complete right bundle branch block", "BUNDLE BRANCH BLOCK, FAMILIAL ISOLATED COMPLETE RIGHT", "Bundle Branch Block, Familial Isolated Complete Right", "bundle branch block, familial isolated complete right", "Familial isolated complete right bundle branch block (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bundle branch block, familial isolated complete right", "shortest_name_length": 52}
{"curie": "UMLS:C1336377", "names": ["Stage IVB Liver Cancer", "Stage IVB Liver Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Liver Cancer", "shortest_name_length": 22}
{"curie": "UMLS:C1274470", "names": ["onychomycosis toenail", "onychomycosis of toenail", "onychomycosis of toenails", "Onychomycosis of toenails", "onychomycosis of toenail (diagnosis)", "Onychomycosis of toenails (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Onychomycosis of toenails", "shortest_name_length": 21}
{"curie": "MONDO:0007931", "names": ["BMD", "VMD2", "BVMD", "Best disease", "BEST1 retinopathy", "Best macular dystrophy", "vitelliform macular dystrophy 2", "macular dystrophy, vitelliform, 2", "Vitelliform Macular Dystrophy Type 2", "vitelliform macular dystrophy type 2", "vitelliform macular dystrophy, type 2", "macular dystrophy, vitelliform, type 2", "early-onset vitelliform macular dystrophy", "VITELLIFORM MACULAR DYSTROPHY, EARLY-ONSET", "Vitelliform Macular Dystrophy, Early-Onset", "Vitelliform Macular Dystrophy, Early Onset", "vitelliform macular dystrophy, early-onset", "polymorphic vitelline macular degeneration", "macular Degeneration, polymorphic vitelline", "macular degeneration, polymorphic vitelline", "juvenile-onset vitelliform macular dystrophy", "Juvenile-Onset Vitelliform Macular Dystrophy", "Juvenile Onset Vitelliform Macular Dystrophy", "vitelliform macular dystrophy, juvenile-onset", "VITELLIFORM MACULAR DYSTROPHY, JUVENILE-ONSET", "Vitelliform Macular Dystrophy, Juvenile Onset", "Vitelliform Macular Dystrophy, Juvenile-Onset", "Best Vitelliform Macular Dystrophy, Multifocal", "BEST VITELLIFORM MACULAR DYSTROPHY, MULTIFOCAL", "Best vitelliform macular dystrophy, multifocal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitelliform macular dystrophy 2", "shortest_name_length": 3}
{"curie": "UMLS:C5237422", "names": ["Refractory Renal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Renal Cell Carcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C4521811", "names": ["Stage IIC Appendix Cancer", "Stage IIC Appendix Carcinoma AJCC v8", "Stage IIC Appendiceal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIC Appendix Carcinoma AJCC v8", "shortest_name_length": 25}
{"curie": "UMLS:C5204282", "names": ["Middle", "Kidney Tumor, Middle Section"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kidney Tumor, Middle Section", "shortest_name_length": 6}
{"curie": "UMLS:C0856022", "names": ["Relapsed Splenic Marginal Zone Lymphoma", "Splenic marginal zone lymphoma recurrent", "Recurrent Splenic Marginal Zone Lymphoma", "Recurrent Splenic Marginal Zone B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Splenic marginal zone lymphoma recurrent", "shortest_name_length": 39}
{"curie": "MONDO:0008148", "names": ["OI4", "OI type 4", "OI, type 4", "OI type IV", "OI, TYPE IV", "osteogenesis imperfecta type 4", "Osteogenesis imperfecta type 4", "Osteogenesis Imperfecta Type IV", "osteogenesis imperfecta, type 4", "Osteogenesis imperfecta type IV", "osteogenesis imperfecta type IV", "Osteogenesis imperfecta, type 4", "Osteogenesis Imperfecta, Type IV", "Osteogenesis imperfecta, type IV", "OSTEOGENESIS IMPERFECTA, TYPE IV", "osteogenesis imperfecta, type IV", "common variable OI with normal sclerae", "Osteogenesis imperfecta type IV (disorder)", "[OBSOLETE] Osteogenesis imperfecta, type 4", "osteogenesis imperfecta with normal sclera", "OI, type 4 Osteogenesis imperfecta, type 4", "osteogenesis imperfecta type IV (diagnosis)", "osteogenesis imperfecta with normal sclerae", "OSTEOGENESIS IMPERFECTA WITH NORMAL SCLERAE", "OI, type IV Osteogenesis imperfecta, type IV", "Osteogenesis imperfecta with normal sclerae, dominant form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteogenesis imperfecta type 4", "shortest_name_length": 3}
{"curie": "UMLS:C2936848", "names": ["Acatalasemia Swiss Type", "Acatalasemia Swiss type", "Swiss Type, Acatalasemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acatalasemia Swiss type", "shortest_name_length": 23}
{"curie": "MONDO:0035737", "names": ["acquired factor V deficiency", "Acquired factor V deficiency", "Acquired Factor V Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired factor V deficiency", "shortest_name_length": 28}
{"curie": "MONDO:0001754", "names": ["eclampsia", "Eclampsia", "ECLAMPSIA", "Eclampsias", "Eclampsia NOS", "Eclamptic toxemia", "Eclamptic toxaemia", "toxemia; eclamptic", "eclamptic; toxemia", "Eclampsia (disorder)", "postpartum eclampsia", "Postpartum eclampsia", "ECLAMPSIA POSTPARTUM", "postpartum; eclampsia", "eclampsia (diagnosis)", "Eclampsia, postpartum", "puerperium; eclampsia", "eclampsia, postpartum", "eclampsia; postpartum", "Eclampsia in puerperium", "eclampsia in puerperium", "Toxemia with convulsions", "Toxaemia with convulsions", "Eclampsia in the puerperium", "Eclampsia in puerperium (disorder)", "Eclampsia, unspecified as to time period", "Eclampsia, postpartum condition or complication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eclampsia", "shortest_name_length": 9}
{"curie": "UMLS:C0333897", "names": ["Mild Koilocytotic Atypia", "Mild koilocytotic atypia", "Mild koilocytotic atypia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mild koilocytotic atypia", "shortest_name_length": 24}
{"curie": "UMLS:C4526752", "names": ["Recurrent Diffuse Intrinsic Pontine Glioma", "Recurrent Diffuse Intrinsic Pontine Glioma (DIPG)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Diffuse Intrinsic Pontine Glioma", "shortest_name_length": 42}
{"curie": "MONDO:0012460", "names": ["DFNB67", "autosomal recessive deafness 67", "Deafness, Autosomal Recessive 67", "deafness, autosomal recessive 67", "DEAFNESS, AUTOSOMAL RECESSIVE 67", "deafness, autosomal recessive type 67", "autosomal recessive nonsyndromic deafness 67", "autosomal recessive nonsyndromic hearing loss 67", "LHFPL5 autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic deafness type 67", "autosomal recessive nonsyndromic deafness caused by mutation in LHFPL5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 67", "shortest_name_length": 6}
{"curie": "UMLS:C0041848", "names": ["Idiopathic Neuropathy", "neuropathy; idiopathic", "Unspecified idiopathic peripheral neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unspecified idiopathic peripheral neuropathy", "shortest_name_length": 21}
{"curie": "UMLS:C1518699", "names": ["Ovarian Dermoid Cyst with Leiomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Dermoid Cyst with Leiomyosarcoma", "shortest_name_length": 40}
{"curie": "MONDO:0019866", "names": ["mosaic trisomy 5", "Mosaic trisomy 5", "trisomy 5 mosaicism", "Trisomy 5 mosaicism", "Mosaic trisomy type 5", "Uniparental disomy of 5", "Mosaic trisomy 5 syndrome", "Mosaic trisomy chromosome 5", "Mosaic trisomy of chromosome 5", "Chromosome 5, uniparental disomy", "Mosaic trisomy 5 syndrome (disorder)", "Mosaic trisomy 5 syndrome (diagnosis)", "anomaly of chromosome pair mosaic trisomy 5 syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mosaic trisomy 5", "shortest_name_length": 16}
{"curie": "MONDO:0000166", "names": ["encephalopathy, acute, infection-induced"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephalopathy, acute, infection-induced", "shortest_name_length": 40}
{"curie": "UMLS:C1140716", "names": ["Hypoxic brain injury", "hypoxic brain damage", "Hypoxic brain damage", "Hypoxic Brain Damage", "hypoxic brain injury", "Damage, Hypoxic Brain", "Brain Damage, Hypoxic", "hypoxic brain injuries", "encephalopathy hypoxic", "ENCEPHALOPATHY HYPOXIC", "Hypoxic encephalopathy", "hypoxic encephalopathy", "Hypoxic Encephalopathy", "Encephalopathy, Hypoxic", "Hypoxic Encephalopathies", "Encephalopathies, Hypoxic", "Brain damage due to hypoxia", "Brain disorder resulting from a period of impaired oxygen delivery to the brain", "Brain disorder resulting from a period of impaired oxygen delivery to the brain (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypoxic Brain Damage", "shortest_name_length": 20}
{"curie": "MONDO:0016730", "names": ["GNC", "Gangliocytoma", "gangliocytoma", "Ganglioneuroma", "gangliocytoma of central nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gangliocytoma", "shortest_name_length": 3}
{"curie": "MONDO:0006862", "names": ["pain syndrome myofascial", "Myofascial pain syndrome", "myofascial pain syndrome", "Myofascial Pain Syndrome", "MYOFASCIAL PAIN SYNDROME", "Myofascial Pain Syndromes", "myofascial pain syndromes", "Syndrome, Myofascial Pain", "Myofascial pain syndromes", "Pain Syndrome, Myofascial", "Pain Syndromes, Myofascial", "Syndromes, Myofascial Pain", "myofascial pain syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myofascial pain syndrome", "shortest_name_length": 24}
{"curie": "UMLS:C4521720", "names": ["Stage IV Esophageal Adenocarcinoma", "Postneoadjuvant Therapy Stage IV Esophageal Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postneoadjuvant Therapy Stage IV Esophageal Adenocarcinoma AJCC v8", "shortest_name_length": 34}
{"curie": "MONDO:0015494", "names": ["Pure dystonia", "isolated dystonia", "isolated dystonic disorder", "nonsyndromic dystonic disorder", "nonsyndromic dystonia (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated dystonia", "shortest_name_length": 13}
{"curie": "MONDO:0035707", "names": ["blepharophimosis-intellectual disability syndrome/genitopatellar overlap syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blepharophimosis-intellectual disability syndrome/genitopatellar overlap syndrome", "shortest_name_length": 81}
{"curie": "UMLS:C0748536", "names": ["Scleral bleeding", "Scleral hemorrhage", "scleral hemorrhage", "SCLERAL HEMORRHAGE", "Scleral haemorrhage", "hemorrhages scleral", "Hemorrhage of sclera", "Hemorrhage of sclera (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemorrhage of sclera", "shortest_name_length": 16}
{"curie": "MONDO:0032565", "names": ["EORVA", "OPHTHALMOPLEGIA, EXTERNAL, WITH RIB AND VERTEBRAL ANOMALIES", "ophthalmoplegia, external, with rib and vertebral anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ophthalmoplegia, external, with rib and vertebral anomalies", "shortest_name_length": 5}
{"curie": "MONDO:0011551", "names": ["DYT5b", "Th-Deficient Drd", "Segawa syndrome, recessive", "TYROSINE HYDROXYLASE DEFICIENCY", "Tyrosine Hydroxylase Deficiency", "Tyrosine hydroxylase deficiency", "Autosomal recessive Segawa syndrome", "autosomal recessive Segawa syndrome", "Segawa Syndrome, Autosomal Recessive", "SEGAWA SYNDROME, AUTOSOMAL RECESSIVE", "Segawa syndrome, autosomal recessive", "TH-deficient dopa-responsive dystonia", "Autosomal Recessive Infantile Parkinsonism", "PARKINSONISM, INFANTILE, AUTOSOMAL RECESSIVE", "Parkinsonism, Infantile, Autosomal Recessive", "Autosomal recessive dopa responsive dystonia", "autosomal recessive dopa-responsive dystonia", "Parkinsonism, infantile, autosomal recessive", "Autosomal recessive dopa-responsive dystonia", "dopa-responsive dystonia, autosomal recessive", "Dopa-responsive dystonia, autosomal recessive", "Dopa-Responsive Dystonia, Autosomal Recessive", "DOPA-RESPONSIVE DYSTONIA, AUTOSOMAL RECESSIVE", "DOPA responsive dystonia, autosomal recessive", "Dystonia, DOPA responsive, autosomal recessive", "dystonia, Dopa-responsive, autosomal recessive", "DYSTONIA, DOPA-RESPONSIVE, AUTOSOMAL RECESSIVE", "Dystonia, Dopa-Responsive, Autosomal Recessive", "dystonia, DOPA responsive, autosomal recessive", "Tyrosine hydroxylase-deficient dopa-responsive dystonia", "tyrosine hydroxylase-deficient dopa-responsive dystonia", "Tyrosine hydroxylase deficient dopa responsive dystonia", "Autosomal recessive dopa responsive dystonia (disorder)", "Dystonia, Dopa-Responsive, With Or Without Hyperphenylalaninemia, Autosomal Recessive", "DYSTONIA, DOPA-RESPONSIVE, WITH OR WITHOUT HYPERPHENYLALANINEMIA, AUTOSOMAL RECESSIVE", "DYSTONIA, DOPA-RESPONSIVE, WITH OR WITHOUT HYPERPHENYLALANINEMIA, AUTOSOMAL RECESSIVE (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "TH-deficient dopa-responsive dystonia", "shortest_name_length": 5}
{"curie": "MONDO:0014298", "names": ["chromosome 5q12 deletion syndrome", "PDE4D haploinsufficiency syndrome", "CHROMOSOME 5q12 DELETION SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 5q12 deletion syndrome", "shortest_name_length": 33}
{"curie": "MONDO:0018634", "names": ["amyloidosis familial", "Familial amyloidosis", "familial amyloidosis", "Familial Amyloidosis", "amyloidosis; genetic", "genetic; amyloidosis", "Familial Amyloidoses", "Amyloidoses, Familial", "familial; amyloidosis", "amyloidosis; familial", "Amyloidosis, Familial", "amyloidosis, Familial", "Hereditary Amyloidoses", "Hereditary Amyloidosis", "hereditary amyloidosis", "Hereditary amyloidosis", "amyloidosis hereditary", "Amyloidoses, Hereditary", "Amyloidosis, Hereditary", "hereditary amyloidosis (disease)", "Hereditary amyloidosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary amyloidosis", "shortest_name_length": 20}
{"curie": "OMIM:614009", "names": ["BDPLT13", "BLEEDING DISORDER, PLATELET-TYPE, 13, SUSCEPTIBILITY TO", "BLEEDING DISORDER, SUSCEPTIBILITY TO, DUE TO DEFECTIVE PLATELET THROMBOXANE A2 RECEPTOR"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 7}
{"curie": "MONDO:0001393", "names": ["peripheral focal chorioretinitis", "Peripheral focal chorioretinitis", "focal peripheral chorioretinitis", "focal peripheral chorioretinitis (diagnosis)", "Peripheral focal choroiditis AND chorioretinitis", "Peripheral focal choroiditis and chorioretinitis", "chorioretinitis focal peripheral and choroiditis", "Focal choroiditis and chorioretinitis, peripheral", "Peripheral focal choroiditis AND chorioretinitis (disorder)", "Peripheral focal choroiditis AND chorioretinitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peripheral focal chorioretinitis", "shortest_name_length": 32}
{"curie": "MONDO:0003438", "names": ["CSCLC", "combined type SCLC", "SCLC, combined type", "combined small cell lung cancer", "Combined Small Cell Lung Cancer", "combined small cell lung carcinoma", "Combined Lung Small Cell Carcinoma", "Combined Small Cell Lung Carcinoma", "combined type small cell lung cancer", "Combined Small Cell Carcinoma of Lung", "combined small cell carcinoma of lung", "small cell lung cancer, combined type", "lung cancer, combined type, small cell", "lung combined type small cell carcinoma", "Combined Type Small Cell Lung Carcinoma", "combined type small cell lung carcinoma", "small cell and large cell lung carcinoma", "Small Cell and Large Cell Lung Carcinoma", "Combined Small Cell Carcinoma of the Lung", "Combined small cell carcinoma of the lung", "combined small cell carcinoma of the lung", "combined small and large cell lung cancer", "Combined Small and Large Cell Lung Cancer", "Combined Type Small Cell Carcinoma of Lung", "combined type small cell carcinoma of lung", "small cell and large cell carcinoma of lung", "Small Cell and Large Cell Carcinoma of Lung", "combined small and large cell lung carcinoma", "Combined Small and Large Cell Lung Carcinoma", "Mixed Small Cell and Large Cell Lung Carcinoma", "mixed small cell and large cell lung carcinoma", "Combined Type Small Cell Carcinoma of the Lung", "combined type small cell carcinoma of the lung", "Small Cell and Large Cell Carcinoma of the Lung", "small cell and large cell carcinoma of the lung", "Combined Small Cell and Large Cell Lung Carcinoma", "combined small cell carcinoma of lung (diagnosis)", "Mixed Small Cell and Large Cell Carcinoma of Lung", "combined small cell and large cell lung carcinoma", "mixed small cell and large cell carcinoma of lung", "Mixed Small Cell and Large Cell Carcinoma of the Lung", "mixed small cell and large cell carcinoma of the lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined small cell lung carcinoma", "shortest_name_length": 5}
{"curie": "MONDO:0004337", "names": ["Anal Margin Paget Disease", "Anal margin Paget's disease", "perianal skin Paget disease", "Anal Margin Paget's Disease", "anal margin Paget's disease", "perianal skin Paget's disease", "Perianal Skin Paget's Disease", "Paget's disease of anal margin", "extramammary; Paget, anal, skin", "Paget; extramammary, anal, skin", "Paget Disease of the Anal Margin", "Paget disease of the anal margin", "Paget; extramammary, anal, margin", "extramammary; Paget, anal, margin", "Paget's disease of the anal margin", "Paget's Disease of the Anal Margin", "perianal skin mammary Paget's disease", "Paget's disease of anal margin (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "perianal skin Paget disease", "shortest_name_length": 25}
{"curie": "MONDO:0003608", "names": ["Optic atrophy", "Optic Atrophy", "OPTIC ATROPHY", "atrophy optic", "Atrophy optic", "optic atrophy", "Atrophy, Optic", "OA - Optic atrophy", "optic disc atrophy", "Optic disc atrophy", "n.opticus; atrophy", "Optic atrophy, NOS", "optic nerve atrophy", "Optic nerve atrophy", "OPTIC NERVE ATROPHY", "ATROPHY OPTIC NERVE", "Atrophy optic nerve", "Optic disc atrophied", "atrophy nerves optic", "atrophy; optic nerve", "atrophy of optic disc", "Atrophy of optic disc", "atrophied nerve optic", "Complete optic atrophy", "Optic atrophy (disorder)", "Optic-nerve degeneration", "optic atrophy (diagnosis)", "Unspecified optic atrophy", "Optic atrophy, unspecified", "Atrophy of whole optic disc", "complete optic nerve atrophy", "optic nerve atrophy complete", "optic disc atrophy (diagnosis)", "Atrophy of optic disc (disorder)", "Complete optic atrophy (disorder)", "CRANIAL NERVE II OPTIC NERVE ATROPHY", "complete optic nerve atrophy (diagnosis)", "atrophy of optic disc (physical finding)", "nerve; atrophy, cranial nerve, second (optic)", "atrophy; nerve, cranial nerve, second (optic)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "optic atrophy", "shortest_name_length": 13}
{"curie": "MONDO:0001196", "names": ["Coitalgia", "DYSPAREUNIA", "Dyspareunia", "Painful coitus", "Coitus painful", "Coitalgia, NOS", "Pain on coitus", "Dyspareunia NOS", "Dyspareunia, NOS", "Pain on intercourse", "Painful intercourse", "Dyspareunia (finding)", "Nonorganic dyspareunia", "functional dyspareunia", "dyspareunia; nonorganic", "Dyspareunia psychogenic", "non-organic dyspareunia", "psychologic dyspareunia", "Non-organic dyspareunia", "Dyspareunia;psychogenic", "Psychogenic dyspareunia", "psychogenic dyspareunia", "Psychologic dyspareunia", "dyspareunia, psychogenic", "Dyspareunia, psychogenic", "Pain on sexual intercourse", "nonorganic origin; dyspareunia", "Psychologic dyspareunia (disorder)", "Psychologic painful sexual act of female", "dyspareunia not due to physical condition", "dyspareunia not due to physical condition (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "psychologic dyspareunia", "shortest_name_length": 9}
{"curie": "MONDO:0032689", "names": ["RP85", "retinitis pigmentosa 85", "RETINITIS PIGMENTOSA 85"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 85", "shortest_name_length": 4}
{"curie": "UMLS:C0521570", "names": ["Retinal AVM/H", "Retinal arteriovenous anomaly", "Retinal Arteriovenous Malformation", "Retinal arteriovenous malformation", "Congenital retinal arteriovenous anastomoses", "Retinal arteriovenous malformation (disorder)", "Retinal Arteriovenous Malformation/Hemangioma", "Congenital retinal arteriovenous communication", "Congenital arteriovenous malformation of retina", "Congenital arteriovenous anastomoses of the retina", "Congenital arteriovenous communication of the retina"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retinal arteriovenous malformation", "shortest_name_length": 13}
{"curie": "UMLS:C1333179", "names": ["Skin Radiation-Related Angiosarcoma", "Cutaneous Radiation-Related Angiosarcoma", "Cutaneous Radiation-Induced Angiosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin Radiation-Related Angiosarcoma", "shortest_name_length": 35}
{"curie": "MONDO:0011187", "names": ["PAPA2", "Papa2", "postaxial polydactyly, type A2", "POSTAXIAL POLYDACTYLY, TYPE A2", "Postaxial Polydactyly, Type A2", "POLYDACTYLY, POSTAXIAL, TYPE A2", "Polydactyly, Postaxial, Type A2", "polydactyly, postaxial, type A2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polydactyly, postaxial, type A2", "shortest_name_length": 5}
{"curie": "MONDO:0009529", "names": ["DLDD", "E3 deficiency", "E3 DEFICIENCY", "Dld deficiency", "DLD deficiency", "DLD DEFICIENCY", "Diaphorase deficiency", "diaphorase; deficiency", "deficiency; diaphorase", "Deficiency of diaphorase", "NADH diaphorase deficiency", "NADH diaphorase; deficiency", "Cytochrome-b reductase deficiency", "maple syrup urine disease, type 3", "Lipoamide dehydrogenase deficiency", "Cytochrome b5 reductase deficiency", "maple syrup urine disease, type III", "Maple syrup urine disease, type III", "MAPLE SYRUP URINE DISEASE, TYPE III", "pyruvate dehydrogenase E3 deficiency", "Pyruvate dehydrogenase E3 deficiency", "Lactic acidosis due to LAD deficiency", "Deficiency of cytochrome-b5 reductase", "Dihydrolipoyl dehydrogenase deficiency", "E3-deficient maple syrup urine disease", "DPNH methemoglobin reductase deficiency", "NADH cytochrome B5 reductase deficiency", "NADH methemoglobin reductase deficiency", "NADH-methemoglobin reductase deficiency", "Deficiency of cytochrome-b>5< reductase", "NADH cytochrome b5 reductase deficiency", "NADH-CYTOCHROME b5 REDUCTASE DEFICIENCY", "Nadh-Cytochrome B5 Reductase Deficiency", "Deficiency of lipoamide reductase (NADH)", "NADH-methaemoglobin reductase deficiency", "DPNH methaemoglobin reductase deficiency", "deficiency; NADH-methemoglobin reductase", "NADH-methemoglobin reductase; deficiency", "DIHYDROLIPOAMIDE DEHYDROGENASE DEFICIENCY", "Dihydrolipoamide dehydrogenase deficiency", "dihydrolipoamide dehydrogenase deficiency", "Deficiency of dihydrolipoamide dehydrogenase", "Maple syrup urine disease with lactic acidosis", "DLD - Dihydrolipoamide dehydrogenase deficiency", "Deficiency of cytochrome-b<sub>5</sub> reductase", "Deficiency of cytochrome-b5 reductase (disorder)", "Autosomal recessive congenital methemoglobinemia", "NADH-DEPENDENT METHEMOGLOBIN REDUCTASE DEFICIENCY", "NADH-dependent methemoglobin reductase deficiency", "Congenital DPNH-methemoglobin-reductase deficiency", "Autosomal recessive congenital methaemoglobinaemia", "hereditary NADH methemoglobin reductase deficiency", "Congenital NADH-methemoglobin reductase deficiency", "Congenital NADH-methemoglobin-reductase deficiency", "Deficiency of cytochrome-b>5< reductase (disorder)", "Methemoglobinemia, Congenital, Autosomal Recessive", "METHEMOGLOBINEMIA, CONGENITAL, AUTOSOMAL RECESSIVE", "Chronic familial methemoglobin reductase deficiency", "Congenital NADH-methaemoglobin reductase deficiency", "Chronic familial methaemoglobin reductase deficiency", "Dihydrolipoamide dehydrogenase deficiency (disorder)", "LIPOAMIDE DEHYDROGENASE DEFICIENCY, LACTIC ACIDOSIS DUE TO", "lipoamide dehydrogenase deficiency, lactic acidosis due to", "Congenital infantile lactic acidosis due to LAD deficiency", "Autosomal recessive congenital methemoglobinemia (disorder)", "Deficiency of cytochrome-b<sub>5</sub> reductase (disorder)", "METHEMOGLOBINEMIA DUE TO DEFICIENCY OF METHEMOGLOBIN REDUCTASE", "Methemoglobinemia due to deficiency of methemoglobin reductase", "hereditary NADH methemoglobin reductase deficiency (diagnosis)", "Congenital methemoglobinemia due to NADH-cytochrome b5 reductase 3 deficiency", "Congenital methaemoglobinaemia due to NADH-cytochrome b5 reductase 3 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyruvate dehydrogenase E3 deficiency", "shortest_name_length": 4}
{"curie": "UMLS:C2984092", "names": ["Hepatocellular Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatocellular Carcinoma by AJCC v7 Stage", "shortest_name_length": 41}
{"curie": "MONDO:0007830", "names": ["INSENSITIVITY TO PAIN WITH HYPERPLASTIC MYELINOPATHY", "insensitivity to pain with hyperplastic Myelinopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "insensitivity to pain with hyperplastic Myelinopathy", "shortest_name_length": 52}
{"curie": "MONDO:0014210", "names": ["MRT37", "mental retardation, autosomal recessive 37", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 37", "mental retardation, autosomal recessive, 37", "intellectual disability, autosomal recessive 37", "mental retardation, autosomal recessive type 37", "intellectual disability, autosomal recessive type 37", "autosomal recessive intellectual developmental disorder 37", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 37", "intellectual disability-hypotonia-spasticity-sleep disorder syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability-hypotonia-spasticity-sleep disorder syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C1266126", "names": ["PFHT", "Plexiform fibrohistiocytic tumor", "Plexiform Fibrohistiocytic Tumor", "Plexiform fibrohistiocytic tumour", "Plexiform Fibrohistiocytic Neoplasm", "Plexiform fibrohistiocytic tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Plexiform fibrohistiocytic tumor", "shortest_name_length": 4}
{"curie": "MONDO:0035312", "names": ["fibrohistiocytic inflammatory pseudotumor of the liver"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibrohistiocytic inflammatory pseudotumor of the liver", "shortest_name_length": 54}
{"curie": "MONDO:0005373", "names": ["Meningococcal disease", "Meningococcal Disease", "meningococcal disease", "disease meningococcal", "Meningococcal Diseases", "meningococcal diseases", "Meningococcal diseases", "Meningococcal Infection", "meningococcal infection", "Infection;meningococcal", "Meningococcal infection", "meningococcal; infection", "Infection, Meningococcal", "infection; meningococcal", "Meningococcal Infections", "MENINGOCOCCAL INFECTIONS", "meningococcal infections", "Infections, Meningococcal", "Meningococcal disease NOS", "Meningococcal infection NOS", "Meningococcal infection, NOS", "Neisseria meningitidis infection", "Meningococcal infectious disease", "infections, Neisseria meningitidis", "Unspecified meningococcal infection", "meningococcal infection (diagnosis)", "Neisseria meningitidis infection NOS", "Meningococcal infection, unspecified", "Meningococcal infectious disease, NOS", "Infection due to Neisseria meningitidis", "Meningococcal infectious disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "meningococcal infection", "shortest_name_length": 21}
{"curie": "MONDO:0045068", "names": ["minor salivary gland adenoid cystic carcinoma", "Minor Salivary Gland Adenoid Cystic Carcinoma", "Adenoid Cystic Carcinoma of Minor Salivary Gland", "adenoid cystic carcinoma of minor salivary gland", "Adenoid Cystic Carcinoma of the Minor Salivary Gland", "adenoid cystic carcinoma of the minor salivary gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "minor salivary gland adenoid cystic carcinoma", "shortest_name_length": 45}
{"curie": "UMLS:C4745008", "names": ["Malignant Peritoneal and Retroperitoneal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Peritoneal and Retroperitoneal Neoplasm", "shortest_name_length": 49}
{"curie": "MONDO:0018432", "names": ["papular mucinosis", "lichenoid myxedema", "lichen myxedematosus", "lichen myxoedematosus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lichen myxedematosus", "shortest_name_length": 17}
{"curie": "UMLS:C4054916", "names": ["Functioning PitNET/Microadenoma", "Functional Pituitary Microadenoma", "Functioning Pituitary Gland Microadenoma", "Functioning Pituitary Neuroendocrine Tumor/Microadenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Functioning Pituitary Neuroendocrine Tumor/Microadenoma", "shortest_name_length": 31}
{"curie": "MONDO:0000341", "names": ["paralytic poliomyelitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paralytic poliomyelitis", "shortest_name_length": 23}
{"curie": "MONDO:0003895", "names": ["PEOS", "Surface Periosteal", "Periosteal osteosarcoma", "periosteal osteosarcoma", "Periosteal Osteosarcoma", "Periosteal osteogenic sarcoma", "periosteal osteogenic sarcoma", "Juxtacortical Chondroblastic Osteosarcoma", "juxtacortical chondroblastic osteosarcoma", "Periosteal osteosarcoma (morphologic abnormality)", "periosteal osteosarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "periosteal osteogenic sarcoma", "shortest_name_length": 4}
{"curie": "MONDO:0011505", "names": ["Fhbl2", "FHBL2", "combined familial hypolipidemia", "ANGPTL3 hypobetalipoproteinemia", "HYPOLIPIDEMIA, FAMILIAL, COMBINED", "hypolipidemia, familial, combined", "familial hypobetalipoproteinemia 2", "Hypobetalipoproteinemia, Familial, 2", "HYPOBETALIPOPROTEINEMIA, FAMILIAL, 2", "hypobetalipoproteinemia, familial, 2", "familial hypobetalipoproteinemia type 2", "hypobetalipoproteinemia, familial, type 2", "hypobetalipoproteinemia caused by mutation in ANGPTL3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial hypobetalipoproteinemia 2", "shortest_name_length": 5}
{"curie": "MONDO:0012987", "names": ["AGM6", "agammaglobulinemia 6", "CD79B autosomal agammaglobulinemia", "agammaglobulinemia 6, autosomal recessive", "AGAMMAGLOBULINEMIA 6, AUTOSOMAL RECESSIVE", "autosomal agammaglobulinemia caused by mutation in CD79B", "agammaglobulinemia, autosomal recessive, due to Cd79B defect", "AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO CD79B DEFECT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "agammaglobulinemia 6, autosomal recessive", "shortest_name_length": 4}
{"curie": "UMLS:C5234880", "names": ["GIDID", "CID-MIA", "CID with multiple intestinal atresia", "GASTROINTESTINAL DEFECTS AND IMMUNODEFICIENCY SYNDROME", "Gastrointestinal Defects And Immunodeficiency Syndrome", "Gastrointestinal Defects and Immunodeficiency Syndrome", "Multiple Intestinal Atresia With Combined Immune Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "GASTROINTESTINAL DEFECTS AND IMMUNODEFICIENCY SYNDROME", "shortest_name_length": 5}
{"curie": "MONDO:0004835", "names": ["fasciitis necrotize", "fascitis necrotizing", "Necrotizing myositis", "Necrotizing Fascitis", "necrotizing myositis", "necrotizing fascitis", "Necrotising myositis", "Fascitis, Necrotizing", "fasciitis necrotising", "necrotizing fasciitis", "Necrotizing fasciitis", "Fasciitis necrotizing", "fasciitis necrotizing", "FASCIITIS NECROTISING", "necrotising fasciitis", "Necrotizing Fasciitis", "Necrotising fasciitis", "FASCIITIS NECROTIZING", "Fasciitis necrotising", "Streptococcal gangrene", "Fasciitis, Necrotizing", "necrotizing cellulitis", "streptococcal gangrene", "Necrotising cellulitis", "FASCIITIS, NECROTIZING", "Necrotizing erysipelas", "Necrotizing cellulitis", "Necrotizing Fascitides", "Necrotizing Fasciitides", "Fascitides, Necrotizing", "Fasciitides, Necrotizing", "Necrotizing fasciitis NOS", "Necrotising fasciitis NOS", "Necrotizing fasciitis (disorder)", "GANGRENE, HEMOLYTIC STREPTOCOCCUS", "necrotizing fasciitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "necrotizing fasciitis", "shortest_name_length": 19}
{"curie": "MONDO:0018022", "names": ["Lepore-beta-thalassemia syndrome", "HbLepore-beta-thalassemia syndrome", "hemoglobin Lepore-beta-thalassemia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemoglobin Lepore-beta-thalassemia syndrome", "shortest_name_length": 32}
{"curie": "MONDO:0012918", "names": ["CILD10", "primary ciliary dyskinesia 10", "CILIARY DYSKINESIA, PRIMARY, 10", "Ciliary Dyskinesia, Primary, 10", "ciliary dyskinesia, primary, 10", "DNAAF2 primary ciliary dyskinesia", "primary ciliary dyskinesia type 10", "ciliary dyskinesia, primary, type 10", "primary ciliary dyskinesia caused by mutation in DNAAF2", "primary ciliary dyskinesia 10 with or without situs inversus", "ciliary dyskinesia, primary, 10, with or without situs inversus", "CILIARY DYSKINESIA, PRIMARY, 10, WITH OR WITHOUT SITUS INVERSUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia 10", "shortest_name_length": 6}
{"curie": "MONDO:0010060", "names": ["IOSCA", "MTDPS7", "OHAHA Syndrome", "OHAHA syndrome", "OHAHA SYNDROME", "SCA8, FORMERLY", "Ohaha syndrome", "SCA8 (formerly)", "spinocerebellar ataxia 8", "spinocerebellar ataxia 8, formerly", "SPINOCEREBELLAR ATAXIA 8, FORMERLY", "spinocerebellar ataxia 8 (formerly)", "Infantile-onset spinocerebellar ataxia", "Infantile onset spinocerebellar ataxia", "Infantile-Onset Spinocerebellar Ataxia", "infantile onset spinocerebellar ataxia", "mitochondrial DNA depletion syndrome 7", "SPINOCEREBELLAR ATAXIA, INFANTILE-ONSET", "spinocerebellar ataxia, infantile-onset", "mitochondrial DNA depletion syndrome type 7", "Infantile onset spinocerebellar ataxia (disorder)", "Spinocerebellar ataxia infantile with sensory neuropathy", "spinocerebellar ataxia infantile with sensory neuropathy", "spinocerebellar ataxia, infantile, with sensory neuropathy", "Spinocerebellar Ataxia, Infantile, with Sensory Neuropathy", "SPINOCEREBELLAR ATAXIA, INFANTILE, WITH SENSORY NEUROPATHY", "mitochondrial DNA depletion syndrome 7 (hepatocerebral type)", "MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE)", "ophthalmoplegia, hypotonia, ataxia, hypacusis, and athetosis", "Ophthalmoplegia, hypotonia, ataxia, hypacusis, and athetosis", "OPHTHALMOPLEGIA, HYPOTONIA, ATAXIA, HYPOACUSIS, AND ATHETOSIS", "ophthalmoplegia - hypotonia - ataxia - hypoacusis - athetosis", "ophthalmoplegia, hypotonia, ataxia, hypoacusis, and athetosis", "ophthalmoplegia-hypotonia-ataxia-hypoacusis-athetosis syndrome", "Ophthalmoplegia-hypotonia-ataxia-hypoacusis-athetosis syndrome", "Ophthalmoplegia, hypotonia, ataxia, hypoacusis, athetosis syndrome", "TWNK autosomal recessive degenerative and progressive cerebellar ataxia", "autosomal recessive degenerative and progressive cerebellar ataxia caused by mutation in TWNK"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial DNA depletion syndrome 7 (hepatocerebral type)", "shortest_name_length": 5}
{"curie": "MONDO:0008317", "names": ["proteolytic capacity of plasma", "PROTEOLYTIC CAPACITY OF PLASMA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "proteolytic capacity of plasma", "shortest_name_length": 30}
{"curie": "UMLS:C0338811", "names": ["latent chronic schizophrenia", "chronic latent schizophrenia", "Latent Chronic Schizophrenia", "Chronic latent schizophrenia", "Latent schizophrenia, chronic", "Latent schizophrenia, chronic state", "Chronic latent schizophrenia (disorder)", "chronic latent schizophrenia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic latent schizophrenia", "shortest_name_length": 28}
{"curie": "MONDO:0021511", "names": ["Benign Adrenal Tumor", "benign adrenal tumor", "benign adrenal neoplasm", "Benign Adrenal Neoplasm", "adrenal benign neoplasm", "Adrenal neoplasms benign", "benign adrenal gland tumor", "Benign Adrenal Gland Tumor", "Benign adrenal neoplasm NOS", "Benign tumor of adrenal gland", "Benign Adrenal Gland Neoplasm", "Benign Tumor of Adrenal Gland", "benign tumor of adrenal gland", "benign adrenal gland neoplasm", "adrenal gland benign neoplasm", "Benign tumour of adrenal gland", "benign neoplasm of adrenal gland", "Benign neoplasm of adrenal gland", "Benign Neoplasm of Adrenal Gland", "benign tumor of the adrenal gland", "Benign Tumor of the Adrenal Gland", "Benign neoplasm of suprarenal gland", "Benign Neoplasm of the Adrenal Gland", "benign neoplasm of the adrenal gland", "Benign neoplasm of adrenal gland (disorder)", "benign neoplasm of adrenal gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of adrenal gland", "shortest_name_length": 20}
{"curie": "MONDO:0006651", "names": ["iridocyclitis", "Iridocyclitis", "uveitis anterior", "Uveitis anterior", "Anterior Uveitis", "Anterior uveitis", "anterior uveitis", "Uveitis, Anterior", "Anterior Uveitides", "Acute iridocyclitis", "acute iridocyclitis", "Uveitides, Anterior", "iridocyclitis acute", "acute; iridocyclitis", "iridocyclitis; acute", "Iridocyclitis, acute", "Anterior uveitis, NOS", "Acute Anterior Uveitis", "acute anterior uveitis", "Acute anterior uveitis", "uveitis anterior acute", "ACUTE ANTERIOR UVEITIS", "Anterior uveitis, acute", "anterior uveitis (disease)", "Anterior uveitis (disorder)", "AAU - acute anterior uveitis", "Anterior uveitis (diagnosis)", "iridocyclitis acute (diagnosis)", "Acute anterior uveitis (disorder)", "Acute anterior uveitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anterior uveitis", "shortest_name_length": 13}
{"curie": "UMLS:C5243783", "names": ["Toxic cardiomyopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Toxic cardiomyopathy", "shortest_name_length": 20}
{"curie": "MONDO:0014431", "names": ["FPLD6", "LIPE-related FPLD", "familial partial lipodystrophy type 6", "LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 6", "lipodystrophy, familial partial, type 6", "LIPE-related familial partial lipodystrophy", "FPLD6 - familial partial lipodystrophy type 6", "familial partial lipodystrophy associated with LIPE mutations", "LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH LIPE MUTATIONS", "lipodystrophy, familial partial, associated with Lipe mutations", "Lipase E, hormone sensitive type-related familial partial lipodystrophy", "Lipase E, hormone sensitive type-related familial partial lipodystrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "LIPE-related familial partial lipodystrophy", "shortest_name_length": 5}
{"curie": "MONDO:0008266", "names": ["PAPA1", "Postaxial hexadactyly", "Postaxial polydactyly", "polydactyly, postaxial", "Polydactyly, Postaxial", "POLYDACTYLY, POSTAXIAL", "Polydactyly, postaxial", "postaxial polydactyly, type A", "postaxial polydactyly, type B", "POSTAXIAL POLYDACTYLY, TYPE A1", "Polydactyly, Postaxial, Type A1", "polydactyly, postaxial, type A1", "POLYDACTYLY, POSTAXIAL, TYPE A1", "polydactyly, postaxial, types A1 and B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polydactyly, postaxial, type A1", "shortest_name_length": 5}
{"curie": "MONDO:0019313", "names": ["Hereditary trophedema", "hereditary lymphedema", "lymphedema, hereditary", "lymphatic malformation", "Hereditary edema of legs", "Hereditary oedema of legs"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphatic malformation", "shortest_name_length": 21}
{"curie": "UMLS:C2987162", "names": ["Pancreatic Mixed Acinar-Ductal Neuroendocrine Carcinoma", "Mixed Acinar-Neuroendocrine-Ductal Carcinoma of the Pancreas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Mixed Acinar-Ductal Neuroendocrine Carcinoma", "shortest_name_length": 55}
{"curie": "UMLS:C1518704", "names": ["Ovarian Dermoid Cyst with Sebaceous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Dermoid Cyst with Sebaceous Carcinoma", "shortest_name_length": 45}
{"curie": "UMLS:C1336212", "names": ["Stage IIIA Ovarian Carcinoma", "FIGO Stage IIIA Ovarian Cancer", "FIGO Stage IIIA Ovarian Carcinoma", "stage IIIA ovarian epithelial cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Ovarian Carcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0015096", "names": ["familial hypofibrinogenemia", "hypofibrinogenemia, familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial hypofibrinogenemia", "shortest_name_length": 27}
{"curie": "MONDO:0013158", "names": ["MDDGA6", "congenital muscular dystrophy-dystroglycanopathy type A6", "Walker-Warburg syndrome or muscle-eye-brain disease, large-related", "Walker-Warburg syndrome or muscle-eye-brain disease, LARGE-related", "WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, LARGE-RELATED", "congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A6", "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6", "Muscular Dystrophy-Dystroglycanopathy (Congenital with Brain and Eye Anomalies) Type A, 6", "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type A, 6", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6", "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6", "shortest_name_length": 6}
{"curie": "UMLS:C5237243", "names": ["Wiesner Nevus", "Combined BAP1-Inactivated Nevus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Combined BAP1-Inactivated Nevus", "shortest_name_length": 13}
{"curie": "UMLS:C0274643", "names": ["phenobarbital toxicity", "PHENOBARBITAL TOXICITY", "Phenobarbital poisoning", "Phenobarbitone poisoning", "Poisoning by phenobarbital", "Poisoning by phenobarbitone", "toxicity from phenobarbital", "Poisoning caused by phenobarbital", "Poisoning caused by phenobarbitone", "phenobarbital toxicity (diagnosis)", "Poisoning caused by phenobarbital (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Poisoning by phenobarbital", "shortest_name_length": 22}
{"curie": "MONDO:0002570", "names": ["HPNS", "HPNSs", "High Pressure Neural Syndrome", "High Pressure Nervous Syndrome", "high pressure nervous syndrome", "High pressure neurologic syndrome", "High Pressure Neurological Syndrome", "high pressure neurological syndrome", "high pressure nervous syndrome (HPNS)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "high pressure neurological syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0014321", "names": ["POF8", "PREMATURE OVARIAN FAILURE 8", "premature ovarian failure 8", "STAG3 primary ovarian failure", "primary ovarian insufficiency 8", "premature ovarian failure type 8", "primary ovarian failure caused by mutation in STAG3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "premature ovarian failure 8", "shortest_name_length": 4}
{"curie": "UMLS:C0396053", "names": ["Singers' Node", "nodes singers", "singer's node", "Singer's node", "nodules singer", "node; singer's", "lump; singer's", "Singer's nodes", "singers' nodes", "teachers; lump", "Singers' nodes", "lump; teachers", "singer's nodes", "Singers' Nodule", "Singers nodules", "singer's nodule", "Singer's nodule", "Screamer's node", "node; vocal cord", "vocal cord; node", "nodules singer's", "vocal cord; lump", "lump; vocal cord", "vocal cord nodule", "Nodular chorditis", "Vocal fold nodule", "VOCAL CORD NODULE", "cord nodule vocal", "Vocal cord nodule", "Vocal Cord Nodule", "vocal cord nodules", "cord nodules vocal", "fold nodules vocal", "Chorditis cantorum", "singer's node; node", "vocal cords nodules", "nodules vocal cords", "cords nodules vocal", "Nodule of Vocal Cord", "Nodule(s);vocal cord", "nodules of vocal cords", "Nodules of vocal cords", "Nodule of the Vocal Cord", "Singers' nodes (disorder)", "singer's nodes (diagnosis)", "singer's nodule of vocal cords", "nodules of vocal cords (diagnosis)", "singer's nodule of vocal cords (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Singers' nodes", "shortest_name_length": 13}
{"curie": "MONDO:8000024", "names": ["ALPS3", "CVID9, FORMERLY", "IMMUNODEFICIENCY, COMMON VARIABLE, 9, FORMERLY", "autoimmune lymphoproliferative syndrome type 3", "autoimmune lymphoproliferative syndrome type III", "AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE III", "autoimmune lymphoproliferative syndrome, type III caused by mutation in PRKCD"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune lymphoproliferative syndrome, type III caused by mutation in PRKCD", "shortest_name_length": 5}
{"curie": "MONDO:0001428", "names": ["Pylorospasm", "pylorospasm", "PYLOROSPASM", "pylorospasms", "pyloric spasm", "SPASM PYLORIC", "Spasm pyloric", "pyloric spasms", "spasm; pylorus", "pylorus; spasm", "Pylorospasm (disorder)", "pylorospasm (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pylorospasm", "shortest_name_length": 11}
{"curie": "UMLS:C0020875", "names": ["Ileal Disease", "ileal disease", "Ileal Diseases", "Disease, Ileal", "ileal diseases", "Diseases, Ileal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ileal Diseases", "shortest_name_length": 13}
{"curie": "UMLS:C5669678", "names": ["Splenic Plasmacytoma", "Plasmacytoma of Spleen", "Primary Splenic Plasmacytoma", "Primary Plasmacytoma of Spleen", "Primary Extraosseous Splenic Plasmacytoma", "Primary Extraosseous Plasmacytoma of Spleen", "Primary Extramedullary Splenic Plasmacytoma", "Primary Extramedullary Plasmacytoma of Spleen"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Splenic Plasmacytoma", "shortest_name_length": 20}
{"curie": "MONDO:0008385", "names": ["Rhiny", "rhiny", "RHINY", "craniorhiny"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rhiny", "shortest_name_length": 5}
{"curie": "UMLS:C4688426", "names": ["IIIA", "Stage IIIA Bladder Cancer", "stage IIIA bladder cancer", "stage IIIA bladder cancer AJCC v8", "Stage IIIA Bladder Cancer AJCC v8", "stage IIIA bladder carcinoma AJCC v8", "Stage IIIA Bladder Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Bladder Cancer AJCC v8", "shortest_name_length": 4}
{"curie": "MONDO:0017299", "names": ["AAOR", "acute annular outer retinopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute annular outer retinopathy", "shortest_name_length": 4}
{"curie": "MONDO:0014221", "names": ["TPID", "TPI deficiency", "TP1 Deficiency", "Deficiency of triosephosphate mutase", "Triosephosphate-Isomerase Deficiency", "Triosephosphate Isomerase Deficiency", "TRIOSEPHOSPHATE ISOMERASE DEFICIENCY", "triosephosphate isomerase deficiency", "Triose phosphate-isomerase deficiency", "triose phosphate isomerase deficiency", "triose phosphate-isomerase deficiency", "Deficiency of phosphotriose isomerase", "Triose phosphate isomerase deficiency", "TPI - Thiose phosphate isomerase deficiency", "Triose phosphate isomerase deficiency (disorder)", "triose phosphate isomerase deficiency (diagnosis)", "hemolytic anemia due to triosephosphate isomerase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "triosephosphate isomerase deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0018828", "names": ["PTORCH2", "USP18 deficiency", "pseudo-TORCH syndrome 2", "PSEUDO-TORCH SYNDROME 2", "Ubiquitin specific peptidase 18 deficiency", "Ubiquitin specific peptidase 18 deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudo-TORCH syndrome 2", "shortest_name_length": 7}
{"curie": "UMLS:C4726607", "names": ["Mixed Phenotype Acute Leukemia, B/T, NOS", "Mixed Phenotype Acute Leukemia, B/T, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mixed Phenotype Acute Leukemia, B/T, Not Otherwise Specified", "shortest_name_length": 40}
{"curie": "UMLS:C4525738", "names": ["Stage IIB Colorectal Neuroendocrine Tumor", "Stage IIB Colorectal Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Colorectal Neuroendocrine Tumor AJCC v8", "shortest_name_length": 41}
{"curie": "MONDO:0006699", "names": ["Choledocholithiasis", "CHOLEDOCHOLITHIASIS", "choledocholithiasis", "cholelithiasis; common duct", "choledocholithiasis (diagnosis)", "Cholelithiasis, Common Bile Duct"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choledocholithiasis", "shortest_name_length": 19}
{"curie": "MONDO:0004820", "names": ["Peripheral Nerve Schwannoma", "peripheral nerve schwannoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peripheral nerve schwannoma", "shortest_name_length": 27}
{"curie": "MONDO:0003836", "names": ["malignant Thyrotropinoma", "Malignant Thyrotropinoma", "malignant thyrotropinoma", "Metastatic TSH-Producing PitNET", "Malignant Pituitary Thyrotropinoma", "malignant pituitary thyrotropinoma", "malignant thyrotropinoma of pituitary", "Malignant Thyrotropinoma of Pituitary", "TSH producing pituitary gland carcinoma", "malignant TSH producing pituitary tumor", "malignant TSH secreting pituitary tumor", "Malignant TSH Secreting Pituitary Tumor", "Malignant TSH Producing Pituitary Tumor", "TSH Producing Pituitary Gland Carcinoma", "TSH-producing pituitary gland carcinoma", "Malignant Pituitary Gland Thyrotropinoma", "malignant pituitary gland thyrotropinoma", "malignant thyrotropinoma of the pituitary", "Malignant Thyrotropinoma of the Pituitary", "malignant TSH producing pituitary neoplasm", "Malignant TSH Producing Tumor of Pituitary", "Malignant TSH Secreting Pituitary Neoplasm", "malignant TSH secreting tumor of pituitary", "malignant TSH producing tumor of pituitary", "Malignant TSH Secreting Tumor of Pituitary", "Malignant TSH Producing Pituitary Neoplasm", "malignant TSH secreting pituitary neoplasm", "Malignant Thyrotropinoma of Pituitary Gland", "malignant thyrotropinoma of pituitary gland", "malignant TSH producing neoplasm of pituitary", "Malignant TSH Producing Neoplasm of Pituitary", "Malignant TSH Secreting Pituitary Gland Tumor", "Malignant TSH Producing Pituitary Gland Tumor", "malignant TSH secreting neoplasm of pituitary", "malignant TSH secreting pituitary gland tumor", "Malignant TSH Secreting Neoplasm of Pituitary", "malignant TSH producing pituitary gland tumor", "Malignant TSH Secreting Tumor of the Pituitary", "Malignant TSH Producing Tumor of the Pituitary", "malignant TSH producing tumor of the pituitary", "malignant TSH secreting tumor of the pituitary", "thyrotropin producing pituitary gland carcinoma", "malignant thyrotropinoma of the pituitary gland", "Malignant Thyrotropinoma of the Pituitary Gland", "Thyrotropin Producing Pituitary Gland Carcinoma", "malignant TSH secreting pituitary gland neoplasm", "malignant TSH producing tumor of pituitary gland", "Malignant TSH Secreting Tumor of Pituitary Gland", "malignant TSH secreting tumor of pituitary gland", "Malignant TSH Producing Pituitary Gland Neoplasm", "malignant TSH producing pituitary gland neoplasm", "Malignant TSH Secreting Pituitary Gland Neoplasm", "Malignant TSH Producing Tumor of Pituitary Gland", "malignant TSH producing neoplasm of the pituitary", "Malignant TSH Producing Neoplasm of the Pituitary", "malignant TSH secreting neoplasm of the pituitary", "Malignant TSH Secreting Neoplasm of the Pituitary", "malignant TSH producing neoplasm of pituitary gland", "Malignant TSH Secreting Neoplasm of Pituitary Gland", "Malignant TSH Producing Neoplasm of Pituitary Gland", "malignant TSH secreting neoplasm of pituitary gland", "malignant TSH secreting tumor of the pituitary gland", "Metastatic Thyrotroph Pituitary Neuroendocrine Tumor", "malignant TSH producing tumor of the pituitary gland", "Malignant TSH Producing Tumor of the Pituitary Gland", "Malignant TSH Secreting Tumor of the Pituitary Gland", "Malignant Thyroid Stimulating Hormone Producing Tumor", "malignant thyroid stimulating hormone producing tumor", "malignant TSH secreting neoplasm of the pituitary gland", "malignant TSH producing neoplasm of the pituitary gland", "Malignant TSH Producing Neoplasm of the Pituitary Gland", "Malignant TSH Secreting Neoplasm of the Pituitary Gland", "Malignant Thyroid Stimulating Hormone Secreting Pituitary Tumor", "malignant thyroid stimulating hormone producing pituitary tumor", "Malignant Thyroid Stimulating Hormone Producing Pituitary Tumor", "malignant thyroid stimulating hormone secreting pituitary tumor", "malignant thyroid stimulating hormone producing tumor of pituitary", "Malignant Thyroid Stimulating Hormone Secreting Tumor of Pituitary", "Malignant Thyroid Stimulating Hormone Producing Tumor of Pituitary", "malignant thyroid stimulating hormone secreting tumor of pituitary", "Malignant Thyroid Stimulating Hormone Producing Pituitary Neoplasm", "malignant thyroid stimulating hormone producing pituitary neoplasm", "malignant thyroid stimulating hormone secreting pituitary neoplasm", "Malignant Thyroid Stimulating Hormone Secreting Pituitary Neoplasm", "malignant thyroid stimulating hormone producing pituitary gland tumor", "malignant thyroid stimulating hormone secreting neoplasm of pituitary", "Malignant Thyroid Stimulating Hormone Secreting Neoplasm of Pituitary", "Malignant Thyroid Stimulating Hormone Producing Neoplasm of Pituitary", "malignant thyroid stimulating hormone producing neoplasm of pituitary", "malignant thyroid stimulating hormone secreting pituitary gland tumor", "Malignant Thyroid Stimulating Hormone Secreting Pituitary Gland Tumor", "Malignant Thyroid Stimulating Hormone Producing Pituitary Gland Tumor", "malignant thyroid stimulating hormone secreting tumor of the pituitary", "Malignant Thyroid Stimulating Hormone Producing Tumor of the Pituitary", "Malignant Thyroid Stimulating Hormone Secreting Tumor of the Pituitary", "malignant thyroid stimulating hormone producing tumor of the pituitary", "malignant thyroid stimulating hormone secreting tumor of pituitary gland", "Malignant Thyroid Stimulating Hormone Secreting Tumor of Pituitary Gland", "Malignant Thyroid Stimulating Hormone Secreting Pituitary Gland Neoplasm", "malignant thyroid stimulating hormone producing tumor of pituitary gland", "malignant thyroid stimulating hormone producing pituitary gland neoplasm", "Malignant Thyroid Stimulating Hormone Producing Pituitary Gland Neoplasm", "malignant thyroid stimulating hormone secreting pituitary gland neoplasm", "Malignant Thyroid Stimulating Hormone Producing Tumor of Pituitary Gland", "malignant thyroid stimulating hormone secreting neoplasm of the pituitary", "Malignant Thyroid Stimulating Hormone Secreting Neoplasm of the Pituitary", "Malignant Thyroid Stimulating Hormone Producing Neoplasm of the Pituitary", "malignant thyroid stimulating hormone producing neoplasm of the pituitary", "Malignant Thyroid Stimulating Hormone Producing Neoplasm of Pituitary Gland", "malignant thyroid stimulating hormone secreting neoplasm of pituitary gland", "Malignant Thyroid Stimulating Hormone Secreting Neoplasm of Pituitary Gland", "malignant thyroid stimulating hormone producing neoplasm of pituitary gland", "Malignant Thyroid Stimulating Hormone Secreting Tumor of the Pituitary Gland", "malignant thyroid stimulating hormone producing tumor of the pituitary gland", "Malignant Thyroid Stimulating Hormone Producing Tumor of the Pituitary Gland", "malignant thyroid stimulating hormone secreting tumor of the pituitary gland", "malignant thyroid stimulating hormone secreting neoplasm of the pituitary gland", "malignant thyroid stimulating hormone producing neoplasm of the pituitary gland", "Malignant Thyroid Stimulating Hormone Producing Neoplasm of the Pituitary Gland", "Malignant Thyroid Stimulating Hormone Secreting Neoplasm of the Pituitary Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant thyroid stimulating hormone producing neoplasm of pituitary gland", "shortest_name_length": 24}
{"curie": "MONDO:0012047", "names": ["Alopecia Universalis Congenita, XY Gonadal Dysgenesis, and Laryngomalacia", "ALOPECIA UNIVERSALIS CONGENITA, XY GONADAL DYSGENESIS, AND LARYNGOMALACIA", "alopecia universalis congenita, XY gonadal dysgenesis, and laryngomalacia", "alopecia universalis congenita, 10Y gonadal dysgenesis, and laryngomalacia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alopecia universalis congenita, 10Y gonadal dysgenesis, and laryngomalacia", "shortest_name_length": 73}
{"curie": "MONDO:0007071", "names": ["Congenital Addison disease", "ADDISON DISEASE, CONGENITAL", "Addison Disease, Congenital", "Addison disease, congenital", "Congenital primary adrenocortical hypofunction", "adrenocortical hypofunction, chronic primary congenital", "ADRENOCORTICAL HYPOFUNCTION, CHRONIC PRIMARY CONGENITAL", "Adrenocortical Hypofunction, Chronic Primary Congenital", "Congenital primary adrenocortical hypofunction (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adrenocortical hypofunction, chronic primary congenital", "shortest_name_length": 26}
{"curie": "MONDO:0013076", "names": ["ADHD7", "susceptibility to attention deficit-hyperactivity disorder 7", "attention deficit-hyperactivity disorder, susceptibility to, 7", "ATTENTION DEFICIT-HYPERACTIVITY DISORDER, SUSCEPTIBILITY TO, 7", "attention Deficit-hyperactivity disorder, susceptibility to, type 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "attention deficit-hyperactivity disorder, susceptibility to, 7", "shortest_name_length": 5}
{"curie": "UMLS:C4523848", "names": ["Sprue-like enteropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sprue-like enteropathy", "shortest_name_length": 22}
{"curie": "UMLS:C4525097", "names": ["Stage IVC Colorectal Cancer AJCC v8", "Stage IVC Colorectal Carcinoma AJCC v8", "Stage IVC Colorectal (Colon or Rectal) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Colorectal Cancer AJCC v8", "shortest_name_length": 35}
{"curie": "UMLS:C4725816", "names": ["Recurrent Malignant Endocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Malignant Endocrine Neoplasm", "shortest_name_length": 38}
{"curie": "MONDO:0012353", "names": ["ECYT3", "familial erythrocytosis 3", "Erythrocytosis, Familial, 3", "erythrocytosis, familial, 3", "ERYTHROCYTOSIS, FAMILIAL, 3", "EGLN1 familial polycythemia", "erythrocytosis, familial, type 3", "familial polycythemia caused by mutation in EGLN1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythrocytosis, familial, 3", "shortest_name_length": 5}
{"curie": "MONDO:0010592", "names": ["FDH", "FODH", "Fodh", "DHOF", "Goltz Syndrome", "goltz syndrome", "GOLTZ SYNDROME", "Goltz syndrome", "Goltzs Syndrome", "Syndrome, Goltz", "Goltz's Syndrome", "Goltz's syndrome", "Syndrome, Goltz's", "GOLTZ-GORLIN SYNDROME", "Jessner-Cole syndrome", "Goltz-Gorlin syndrome", "Goltz Gorlin syndrome", "Goltz Gorlin Syndrome", "Goltz-Gorlin Syndrome", "goltz-gorlin syndrome", "goltz gorlin syndrome", "Syndrome, Goltz Gorlin", "Syndrome, Goltz-Gorlin", "Gorlin Syndrome, Goltz", "Focal dermal hypoplasia", "FOCAL DERMAL HYPOPLASIA", "focal dermal hypoplasia", "Focal Dermal Hypoplasia", "dermal focal hypoplasia", "hypoplasia; focal dermal", "Dermal Hypoplasia, Focal", "focal; dermal hypoplasia", "Hypoplasia, Focal Dermal", "Focal Dermal Hypoplasias", "Liebermann-Cole syndrome", "focal; hypoplasia, dermal", "Hypoplasias, Focal Dermal", "Dermal Hypoplasias, Focal", "FDH - Focal dermal hypoplasia", "Focal facial dermal dysplasia", "FODH - Focal dermal hypoplasia", "Focal dermal hypoplasia syndrome", "focal dermal hypoplasia syndrome", "FOCAL DERMAL HYPOPLASIA SYNDROME", "Focal dermal hypoplasia (disorder)", "Goltz-Peterson-Gorlin-Ravitz syndrome", "focal dermal hypoplasia (FDH) syndrome", "focal dermal hypoplasia, X-linked dominant", "ectodermal and mesodermal dysplasia with osseous involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal dermal hypoplasia", "shortest_name_length": 3}
{"curie": "MONDO:0003873", "names": ["ovarian surface papilloma", "Ovarian Surface Papilloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian surface papilloma", "shortest_name_length": 25}
{"curie": "UMLS:C0029232", "names": ["Organic mood syndrome", "ORGANIC MOOD DISORDER", "organic mood syndrome", "organic mood disorder", "Organic mood disorder", "mood disorder; organic", "organic; mood disorder", "disorder; organic, mood", "disorder; mood, organic", "organic; disorder, mood", "Organic mood disorder, NOS", "Organic affective disorder", "AFFECTIVE SYNDROME ORGANIC", "Organic affective syndrome", "ORGANIC AFFECTIVE SYNDROME", "Organic Affective Syndrome", "organic affective syndrome", "organic affective disorder", "organic; affective disorder", "disorder; affective, organic", "affective; disorder, organic", "organic; disorder, affective", "disorder; organic, affective", "Organic mood disorder (disorder)", "organic mood disorder (diagnosis)", "Organic mood [affective] disorders", "disorder; affective, organic (mixed)", "affective; disorder, organic (mixed)", "medical condition; causing mood disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Organic mood disorder", "shortest_name_length": 21}
{"curie": "MONDO:0000629", "names": ["cardiovascular organ benign neoplasm", "cardiovascular system benign neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiovascular organ benign neoplasm", "shortest_name_length": 36}
{"curie": "UMLS:C4744386", "names": ["Sellar Germinoma", "Germinoma of the Sellar Region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sellar Germinoma", "shortest_name_length": 16}
{"curie": "UMLS:C3897754", "names": ["Recurrent Gemistocytic Astrocytoma", "recurrent childhood gemistocytic astrocytoma", "Recurrent Childhood Gemistocytic Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Gemistocytic Astrocytoma", "shortest_name_length": 34}
{"curie": "MONDO:0020418", "names": ["Dysphagia lusoria", "dysphagia lusoria", "Dysphagia lusoria syndrome", "Dysphagia lusoria (disorder)", "dysphagia lusoria (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dysphagia lusoria", "shortest_name_length": 17}
{"curie": "UMLS:C3494988", "names": ["Malignant hydrocele", "Testicular Malignant Mesothelioma", "Paratesticular Malignant Mesothelioma", "Tunica Vaginalis Malignant Mesothelioma", "malignant mesothelioma of tunica vaginalis", "Malignant mesothelioma of the tunica vaginalis", "neoplasm of tunica vaginalis malignant mesothelioma", "malignant mesothelioma of tunica vaginalis (diagnosis)", "Malignant mesothelioma of the tunica vaginalis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant mesothelioma of the tunica vaginalis", "shortest_name_length": 19}
{"curie": "UMLS:C0853392", "names": ["Stage II Extragonadal Mixed Germ Cell Tumor", "Stage II Extragonadal Primary Mixed Germ Cell Tumor", "Stage II Extragonadal Primary Germ Cell Tumor Mixed", "Extragonadal primary germ cell tumor mixed stage II", "Extragonadal primary germ cell tumour mixed stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extragonadal primary germ cell tumor mixed stage II", "shortest_name_length": 43}
{"curie": "UMLS:C3804981", "names": ["JC virus granule cell neuronopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "JC virus granule cell neuronopathy", "shortest_name_length": 34}
{"curie": "UMLS:C5446548", "names": ["Primary Iris Lymphoma", "Primary Iris Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Iris Non-Hodgkin Lymphoma", "shortest_name_length": 21}
{"curie": "MONDO:0005131", "names": ["cervix cancer", "Cervix Cancer", "Cervical Cancer", "CERVICAL CANCER", "cervical cancer", "Carcinoma;cervix", "carcinoma cervix", "Cancer of Cervix", "Cervix carcinoma", "CERVIX CARCINOMA", "Carcinoma cervix", "CARCINOMA CERVIX", "COLLUM CARCINOMA", "cancer of cervix", "cervix carcinoma", "Cervix Carcinoma", "CERVICAL CARCINOMA", "Cervical carcinoma", "Cervical Carcinoma", "cervical carcinoma", "carcinoma cervical", "Carcinoma of cervix", "Carcinoma of Cervix", "carcinoma of cervix", "CARCINOMA OF CERVIX", "Cervix uteri cancer", "cancer of the cervix", "Cancer of the Cervix", "Cervical cancer, NOS", "cervical cancer, NOS", "Uterine Cervix Cancer", "uterine cervix cancer", "Cervical carcinoma NOS", "carcinoma cervix uteri", "Cervix Uteri Carcinoma", "cervix uteri carcinoma", "Carcinoma of the Cervix", "carcinoma of the cervix", "CARCINOMA UTERINE CERIX", "carcinoma cervix uterine", "Cancer of Uterine Cervix", "Carcinoma uterine cervix", "cancer of uterine cervix", "Uterine Cervix Carcinoma", "uterine cervix carcinoma", "UTERINE CERVIX, CARCINOMA", "Carcinoma of Cervix Uteri", "carcinoma of cervix uteri", "Cervical Cancer (all types)", "carcinoma of uterine cervix", "Carcinoma of Uterine Cervix", "Cancer of the Uterine Cervix", "CARCINOMA OF CERVIX INVASIVE", "cancer of the uterine cervix", "carcinoma of the Cervix Uteri", "carcinoma of the cervix uteri", "Carcinoma of the Cervix Uteri", "CARCINOMA OF CERVIX <INVASIVE>", "Carcinoma of cervix (disorder)", "Carcinoma of the Uterine Cervix", "carcinoma of cervix (diagnosis)", "carcinoma of the uterine cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical carcinoma", "shortest_name_length": 13}
{"curie": "UMLS:C4683594", "names": ["Lugano Classification Childhood Hodgkin Lymphoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Childhood Hodgkin Lymphoma by AJCC v8 Stage", "shortest_name_length": 65}
{"curie": "MONDO:0018763", "names": ["tubulinopathy-associated dysgyria", "brain stem asymmetry-superior cerebellar and basal ganglia dysplasia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tubulinopathy-associated dysgyria", "shortest_name_length": 33}
{"curie": "MONDO:0023521", "names": ["Judge Misch Wright syndrome", "Judge Misch wright syndrome", "Keratodermia palmoplantar periorificial", "keratodermia palmoplantar periorificial", "dry skin, photophobia hyperkeratosis, abnormal fingernails", "Dry skin, photophobia hyperkeratosis, abnormal fingernails", "palmoplantar and perioroficial keratoderma with corneal epithelial dysplasia", "Palmoplantar and perioroficial keratoderma with corneal epithelial dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Judge Misch wright syndrome", "shortest_name_length": 27}
{"curie": "MONDO:0013120", "names": ["SRXY5", "46XY sex reversal 5", "46,XY SEX REVERSAL 5", "46,XY sex reversal 5", "46,XY SEX reversal 5", "46, XY Sex Reversal 5", "46,XY Sex reversal type 5", "Sex Reversal, Xy, Cbx2-Related", "Sex reversal, XY, Cbx2-related", "sex reversal, XY, CBX2-related", "SEX REVERSAL, XY, CBX2-RELATED", "46,XY sex reversal, CBX2-related", "46,XY SEX REVERSAL, CBX2-RELATED", "46,XY Sex reversal, Cbx2-related", "disorder of Sex development, 46,XY, Cbx2-related", "46,XY gonadal dysgenesis, complete, CBX2-related", "46,XY gonadal dysgenesis, complete, Cbx2-related", "46,XY GONADAL DYSGENESIS, COMPLETE, CBX2-RELATED", "Disorder Of Sex Development, 46,Xy, Cbx2-Related", "disorder of sex development, 46,XY, CBX2-related", "46,Xy Gonadal Dysgenesis, Complete, Cbx2-Related", "DISORDER OF SEX DEVELOPMENT, 46,XY, CBX2-RELATED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XY sex reversal 5", "shortest_name_length": 5}
{"curie": "UMLS:C0854506", "names": ["Enterococcal urinary tract infection", "Urinary tract infection enterococcal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urinary tract infection enterococcal", "shortest_name_length": 36}
{"curie": "UMLS:C0748861", "names": ["SMALL CELL CARCINOMA METASTATIC", "Metastatic Small Cell Carcinoma", "Metastatic small cell carcinoma", "small cell carcinoma metastatic", "small cell metastatic carcinoma", "Small cell carcinoma metastatic", "Metastatic Small Cell Neuroendocrine Carcinoma", "Metastatic small cell carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic small cell carcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C4520726", "names": ["Stage I Childhood Hepatoma", "Stage I Pediatric Hepatoma", "Stage I Hepatocellular Cancer", "stage I childhood liver cancer", "Stage I Childhood Liver Cell Carcinoma", "Stage I Pediatric Liver Cell Carcinoma", "Stage I Pediatric Hepatocellular Carcinoma", "Stage I Childhood Hepatocellular Carcinoma AJCC v6", "Stage I Childhood Hepatocellular Carcinoma AJCC v7", "Stage I Childhood Hepatocellular Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Childhood Hepatocellular Carcinoma AJCC v6 and v7", "shortest_name_length": 26}
{"curie": "MONDO:0020147", "names": ["anophthalmia-microphthalmia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anophthalmia-microphthalmia syndrome", "shortest_name_length": 36}
{"curie": "MONDO:0013116", "names": ["MPMCD", "Mitochondrial Complex Deficiency, Combined", "MITOCHONDRIAL COMPLEX DEFICIENCY, COMBINED", "mitochondrial Complex deficiency, combined", "Myopathy With Cataract And Combined Respiratory Chain Deficiency", "myopathy with cataract and combined respiratory chain deficiency", "MYOPATHY WITH CATARACT AND COMBINED RESPIRATORY CHAIN DEFICIENCY", "myopathy with cataract and combined respiratory-chain deficiency", "myopathy, mitochondrial progressive, with congenital cataract and developmental delay", "MYOPATHY, MITOCHONDRIAL PROGRESSIVE, WITH CONGENITAL CATARACT AND DEVELOPMENTAL DELAY", "congenital cataract-progressive muscular hypotonia-deafness-developmental delay syndrome", "congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome", "myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay", "Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0032661", "names": ["NEDIDHA", "neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxia", "NEURODEVELOPMENTAL DISORDER WITH IMPAIRED INTELLECTUAL DEVELOPMENT, HYPOTONIA, AND ATAXIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxia", "shortest_name_length": 7}
{"curie": "UMLS:C0235630", "names": ["RENAL FAILURE AGGRAVATED", "Renal failure aggravated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal failure aggravated", "shortest_name_length": 24}
{"curie": "UMLS:C4054600", "names": ["Undifferentiated High Grade Pleomorphic Sarcoma of Bone", "Localized Childhood Undifferentiated High Grade Pleomorphic Sarcoma", "Localized Childhood Undifferentiated High Grade Pleomorphic Sarcoma of Bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized Childhood Undifferentiated High Grade Pleomorphic Sarcoma of Bone", "shortest_name_length": 55}
{"curie": "MONDO:0017905", "names": ["X-linked MSMD", "X-linked Mendelian susceptibility to mycobacterial disease", "X-linked mendelian susceptibility to mycobacterial disease", "X-linked Mendelian susceptibility to mycobacterial diseases", "X-linked mendelian susceptibility to mycobacterial diseases", "mendelian susceptibility to mycobacterial diseases, X-linked", "X-linked mendelian susceptibility to mycobacterial disease (disorder)", "X-linked Mendelian susceptibility to mycobacterial disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked Mendelian susceptibility to mycobacterial diseases", "shortest_name_length": 13}
{"curie": "MONDO:0012559", "names": ["Primary immunodeficiency syndrome with short stature", "primary immunodeficiency syndrome with short stature", "primary immunodeficiency syndrome due to p14 deficiency", "Primary immunodeficiency syndrome due to p14 deficiency", "Primary immunodeficiency syndrome due to LAMTOR2 deficiency", "immunodeficiency due to defect in MAPBP-interacting PROTEIN", "IMMUNODEFICIENCY DUE TO DEFECT IN MAPBP-INTERACTING PROTEIN", "primary immunodeficiency syndrome due to LAMTOR2 deficiency", "Immunodeficiency due to Defect in MAPBP-Interacting Protein", "immunodeficiency due to defect in Mapbp-interacting Protein", "Primary immunodeficiency syndrome due to p14 deficiency (disorder)", "primary immunodeficiency syndrome due to p14 deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary immunodeficiency syndrome due to p14 deficiency", "shortest_name_length": 52}
{"curie": "MONDO:0020752", "names": ["EJM1", "myoclonic epilepsy, juvenile, susceptibility to, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myoclonic epilepsy, juvenile, susceptibility to, 1", "shortest_name_length": 4}
{"curie": "UMLS:C4520752", "names": ["Stage II Sinonasal Cancer AJCC v6 and v7", "Stage II Sinonasal Carcinoma AJCC v6 and v7", "Stage II Nasal Cavity and Paranasal Sinus Cancer", "Stage II Nasal Cavity and Paranasal Sinus Cancer AJCC v6", "Stage II Nasal Cavity and Paranasal Sinus Cancer AJCC v7", "Stage II Nasal Cavity and Paranasal Sinus Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Nasal Cavity and Paranasal Sinus Cancer AJCC v6 and v7", "shortest_name_length": 40}
{"curie": "MONDO:0012246", "names": ["SCA26", "SPINOCEREBELLAR ATAXIA 26", "Spinocerebellar ataxia 26", "spinocerebellar ataxia 26", "Spinocerebellar ataxia type 26", "spinocerebellar ataxia type 26", "SCA26 Spinocerebellar ataxia 26", "Spinocerebellar ataxia type 26 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia type 26", "shortest_name_length": 5}
{"curie": "MONDO:0100297", "names": ["SSFSC", "SSFSC1", "short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies", "short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 1", "SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 1", "shortest_name_length": 5}
{"curie": "MONDO:0012810", "names": ["ANIB7", "intracranial berry aneurysm 7", "aneurysm, intracranial BERRY, 7", "aneurysm, intracranial berry, 7", "Aneurysm, Intracranial Berry, 7", "ANEURYSM, INTRACRANIAL BERRY, 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aneurysm, intracranial berry, 7", "shortest_name_length": 5}
{"curie": "MONDO:0020749", "names": ["NHD", "PLOSL", "PLOSL1", "NASU-HAKOLA DISEASE", "BRAIN-BONE-FAT DISEASE", "PRESENILE DEMENTIA WITH BONE CYSTS", "DEMENTIA, PREFRONTAL, WITH BONE CYSTS", "DEMENTIA, PROGRESSIVE, WITH LIPOMEMBRANOUS POLYCYSTIC OSTEODYSPLASIA", "polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1", "POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1", "shortest_name_length": 3}
{"curie": "MONDO:0009129", "names": ["dwarfism, proportionate with hip dislocation", "dwarfism, proportionate, with hip dislocation", "Dwarfism, Proportionate, with Hip Dislocation", "DWARFISM, PROPORTIONATE, WITH HIP DISLOCATION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dwarfism, proportionate, with hip dislocation", "shortest_name_length": 44}
{"curie": "MONDO:0100107", "names": ["non-neonatal early infantile epileptic encephalopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-neonatal early infantile epileptic encephalopathy", "shortest_name_length": 53}
{"curie": "MONDO:0003250", "names": ["Myoblastoma", "myoblastoma", "Myoblastomas", "Benign Granular Cell Tumor", "benign granular cell tumor", "granular cell tumor, benign", "GRANULAR CELL TUMOR, BENIGN", "benign granular cell neoplasm", "Benign Granular Cell Neoplasm", "benign granular cell myoblastoma", "Benign Granular Cell Myoblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign granular cell tumor", "shortest_name_length": 11}
{"curie": "MONDO:0019939", "names": ["early-onset schizophrenia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early-onset schizophrenia", "shortest_name_length": 25}
{"curie": "MONDO:0019326", "names": ["phakomatosis cesiomarmorata", "Phakomatosis cesiomarmorata", "Phakomatosis caesiomarmorata", "phakomatosis caesiomarmorata", "Phakomatosis pigmentovascularis type 5", "phakomatosis pigmentovascularis type 5", "Phakomatosis caesiomarmorata (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phakomatosis cesiomarmorata", "shortest_name_length": 27}
{"curie": "MONDO:0014739", "names": ["DFNB97", "autosomal recessive deafness 97", "DEAFNESS, AUTOSOMAL RECESSIVE 97", "deafness, autosomal recessive 97", "deafness, autosomal recessive type 97", "autosomal recessive nonsyndromic deafness 97", "MET autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 97", "autosomal recessive nonsyndromic deafness type 97", "autosomal recessive nonsyndromic deafness caused by mutation in MET"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 97", "shortest_name_length": 6}
{"curie": "MONDO:0020590", "names": ["Mycobacterium", "Mycobacteriosis", "MYCOBACTERIOSES", "mycobacteriosis", "Mycobacterium, NOS", "Mycobacteriosis NOS", "Mycobacteriosis, NOS", "Disease;mycobacterial", "mycobacterial disease", "Mycobacterial disease", "MYCOBACTERIAL DISEASE", "Mycobacterial diseases", "Mycobacterium Infection", "Mycobacterial Infection", "Mycobacterial infection", "mycobacterium infection", "mycobacterial infection", "Mycobacterium Infections", "Infection, Mycobacterium", "Mycobacterium; infection", "infections mycobacterial", "Mycobacterial infections", "infection; Mycobacterium", "Mycobacterial Infections", "Infections, Mycobacterium", "Mycobacteriosis (disorder)", "Mycobacterial infection NOS", "Infection due to mycobacteria", "mycobacterial infectious disease", "Mycobacterial infectious disease", "mycobacterial infection (diagnosis)", "Mycobacterial infection, unspecified", "Unspecified diseases due to mycobacteria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mycobacterial infectious disease", "shortest_name_length": 13}
{"curie": "MONDO:0018547", "names": ["acute tricyclic antidepressant poisoning"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute tricyclic antidepressant poisoning", "shortest_name_length": 40}
{"curie": "UMLS:C4682806", "names": ["Stage III Testicular Cancer", "Stage III Testicular Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Testicular Cancer AJCC v8", "shortest_name_length": 27}
{"curie": "MONDO:0012402", "names": ["Ods1", "ODS1", "opioid dependence, susceptibility to, 1", "OPIOID DEPENDENCE, SUSCEPTIBILITY TO, 1", "opioid dependence, susceptibility to, type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "opioid dependence, susceptibility to, 1", "shortest_name_length": 4}
{"curie": "MONDO:0013246", "names": ["FLD2", "NAFLD2", "FATTY LIVER DISEASE, SUSCEPTIBILITY TO, 2", "fatty liver disease, nonalcoholic, susceptibility to, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fatty liver disease, nonalcoholic, susceptibility to, 2", "shortest_name_length": 4}
{"curie": "MONDO:0008891", "names": ["BVVLS", "BVVLS1", "Fazio-Londe syndrome", "pontobulbar palsy with deafness", "Pontobulbar palsy with deafness", "Brown-Vialetto-van Laere syndrome", "Brown-Vialetto-Van Laere syndrome", "Riboflavin transporter deficiency", "riboflavin transporter deficiency", "Brown-Vialetto-Van Laere syndrome 1", "pontobulbar palsy and neurosensory deafness", "pontobulbar palsy with neurosensory deafness", "progressive bulbar palsy with perceptive deafness", "Progressive bulbar palsy with sensorineural deafness", "progressive bulbar palsy with sensorineural deafness", "hereditary progressive bulbar paralysis with deafness", "riboflavin transmembrane transporter activity disease", "sensorineural hearing loss-pontobulbar palsy syndrome", "disorder of riboflavin transmembrane transporter activity", "Progressive bulbar palsy with sensorineural deafness (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "riboflavin transporter deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C0155216", "names": ["EYELID BLEEDING", "Eyelid bleeding", "eyelid bleeding", "bleeding eyelids", "Eyelid hemorrhage", "eyelid hemorrhage", "Eyelid haemorrhage", "Hemorrhage of eyelid", "Haemorrhage of eyelid", "Hemorrhage of eyelid (disorder)", "eyelid hemorrhage (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemorrhage of eyelid", "shortest_name_length": 15}
{"curie": "UMLS:C0935807", "names": ["Stage III Merkel Cell Cancer", "Stage III Merkel Cell Carcinoma", "stage III Merkel cell carcinoma", "Stage III Merkel Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Merkel Cell Carcinoma AJCC v7", "shortest_name_length": 28}
{"curie": "MONDO:0018540", "names": ["PFAPA", "PFAPA syndrome", "PFAPA Syndrome", "Marshall syndrome", "Marshall Syndrome", "PFAPA syndrome (diagnosis)", "Marshall syndrome with periodic fever", "periodic fever, aphthous stomatitis, pharyngitis and adenitis", "periodic fever-aphtous stomatitis-pharyngitis-adenopathy syndrome", "Periodic fever-aphtous stomatitis-pharyngitis-adenopathy syndrome", "periodic fever, aphthous stomatitis, pharyngitis, adenitis syndrome", "Periodic Fever, Aphthous Stomatitis, Pharyngitis, Adenitis Syndrome", "Syndrome of periodic fever, aphthous stomatitis, pharyngitis, cervical adenitis", "Periodic fever and aphthous stomatitis with pharyngitis and cervical lymphadenitis syndrome", "Periodic fever and aphthous stomatitis with pharyngitis and cervical lymphadenitis syndrome (disorder)", "Periodic fever and aphthous stomatitis with pharyngitis and cervical lymphadenitis syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PFAPA syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0021745", "names": ["child abuse dwarfism", "Child abuse dwarfism", "psychosocial dwarfism", "dwarfism psychosocial", "Psychosocial dwarfism", "Emotional deprivation", "dwarfism; psychosocial", "psychosocial; dwarfism", "deprivation; emotional", "emotional; deprivation", "Kaspar Hauser syndrome", "abuse dwarfism syndrome", "Abuse dwarfism syndrome", "psychosocial short stature", "Emotional deprivation syndrome", "emotional deprivation syndrome", "Emotional deprivation syndrome (disorder)", "emotional deprivation syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "psychosocial short stature", "shortest_name_length": 20}
{"curie": "MONDO:0030346", "names": ["CILD47", "CILIARY DYSKINESIA, PRIMARY, 47, AND LISSENCEPHALY", "ciliary dyskinesia, primary, 47, and lissencephaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ciliary dyskinesia, primary, 47, and lissencephaly", "shortest_name_length": 6}
{"curie": "MONDO:0019025", "names": ["extracutaneous mastocytoma", "Extracutaneous mastocytoma", "Extracutaneous Mastocytoma", "Mastocytoma, Extracutaneous", "Extracutaneous Mastocytomas", "Mastocytomas, Extracutaneous", "Localised extracutaneous mastocytosis", "Localized extracutaneous mastocytosis", "mastocytosis - localized extracutaneous", "Localized extracutaneous mastocytosis (disorder)", "Localized extracutaneous mastocytosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extracutaneous mastocytoma", "shortest_name_length": 26}
{"curie": "UMLS:C1335035", "names": ["PTLD (Polyclonal)", "Non-Destructive PTLD", "Post-Transplant Lymphoproliferative Disorder, Early Lesion", "Non-Neoplastic Post-Transplant Lymphoproliferative Disorder", "Non-Destructive Post-Transplant Lymphoproliferative Disorder", "Post-transplant lymphoproliferative disorder (Polyclonal), NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Destructive Post-Transplant Lymphoproliferative Disorder", "shortest_name_length": 17}
{"curie": "MONDO:0012866", "names": ["FAHN", "SPG35", "hereditary spastic paraplegia 35", "FA2H hereditary spastic paraplegia", "hereditary spastic paraplegia type 35", "autosomal recessive spastic paraplegia 35", "SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE", "spastic paraplegia 35, autosomal recessive", "Autosomal recessive spastic paraplegia type 35", "autosomal recessive spastic paraplegia type 35", "fatty acid hydroxylase-associated neurodegeneration", "familial spastic paraplegia autosomal recessive type 35", "hereditary spastic paraplegia caused by mutation in FA2H", "Autosomal recessive spastic paraplegia type 35 (disorder)", "Autosomal recessive spastic paraplegia type 35 (diagnosis)", "SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE, WITH OR WITHOUT NEURODEGENERATION", "leukodystrophy, dysmyelinating and spastic paraparesis with or without dystonia", "LEUKODYSTROPHY, DYSMYELINATING, AND SPASTIC PARAPARESIS WITH OR WITHOUT DYSTONIA", "Leukodystrophy, Dysmyelinating, And Spastic Paraparesis With Or Without Dystonia", "leukodystrophy, dysmyelinating, and spastic paraparesis with or without dystonia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 35", "shortest_name_length": 4}
{"curie": "MONDO:0021627", "names": ["Capillary Angioma of Lid", "Eyelid Capillary Angioma", "capillary angioma of lid", "eyelid capillary angioma", "Capillary Hemangioma of Lid", "eyelid capillary hemangioma", "capillary angioma of eyelid", "capillary hemangioma of lid", "Capillary Angioma of Eyelid", "Eyelid Capillary Hemangioma", "capillary angioma of the lid", "Capillary Angioma of the Lid", "Capillary Hemangioma of Eyelid", "Capillary hemangioma of eyelid", "capillary hemangioma of eyelid", "Capillary haemangioma of eyelid", "Capillary Angioma of the Eyelid", "Capillary Hemangioma of the Lid", "capillary angioma of the eyelid", "capillary hemangioma of the lid", "Capillary Hemangioma of the Eyelid", "capillary hemangioma of the eyelid", "Capillary hemangioma of eyelid (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eyelid capillary hemangioma", "shortest_name_length": 24}
{"curie": "MONDO:0020792", "names": ["Dwarfism tall vertebrae", "dwarfism with tall vertebrae", "Dwarfism with Tall Vertebrae", "DWARFISM WITH TALL VERTEBRAE", "Short stature and tall vertebrae", "Dwarfism with disproportionately high vertebral bodies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dwarfism with tall vertebrae", "shortest_name_length": 23}
{"curie": "MONDO:0010922", "names": ["Satoyoshi syndrome", "SATOYOSHI SYNDROME", "Komuragaeri disease", "Komuragaeri Disease", "KOMURAGAERI DISEASE", "Satoyoshi syndrome (disorder)", "Satoyoshi syndrome (diagnosis)", "autoimmune disease satoyoshi syndrome", "muscle spasms, intermittent with alopecia, diarrhea and skeletal abnormalities", "Muscle spasms, intermittent with alopecia, diarrhea, and skeletal abnormalities", "MUSCLE SPASMS, INTERMITTENT, WITH ALOPECIA, DIARRHEA, AND SKELETAL ABNORMALITIES", "Muscle Spasms, Intermittent, With Alopecia, Diarrhea, And Skeletal Abnormalities", "muscle spasms, intermittent, with alopecia, diarrhea, and skeletal abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Satoyoshi syndrome", "shortest_name_length": 18}
{"curie": "MONDO:0032863", "names": ["SPGF41", "SPERMATOGENIC FAILURE 41", "spermatogenic failure 41"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 41", "shortest_name_length": 6}
{"curie": "MONDO:0010680", "names": ["EMD1", "EDMD1", "Emerinopathy", "Emerinopathies", "X-Linked Scapuloperoneal Syndrome", "Scapuloperoneal Syndrome, X-Linked", "Scapuloperoneal Syndrome, X Linked", "scapuloperoneal syndrome, X-linked", "Emery-Dreifuss Muscular Dystrophy 1", "Emery-Dreifuss muscular dystrophy 1", "Emery Dreifuss Muscular Dystrophy 1", "Emery Dreifuss Muscular Dystrophy, 1", "Emery-Dreifuss Muscular Dystrophy, 1", "Humeroperoneal neuromuscular disease", "humeroperoneal neuromuscular disease", "Ehlers-Danlos syndrome, classic-like, 1", "X-Linked Emery-Dreifuss Muscular Dystrophy", "X-linked Emery-Dreifuss muscular dystrophy", "X Linked Emery Dreifuss Muscular Dystrophy", "Emery-Dreifuss muscular dystrophy, X-linked", "EMERY-DREIFUSS MUSCULAR DYSTROPHY, X-LINKED", "Emery-Dreifuss Muscular Dystrophy, X-Linked", "Emery Dreifuss Muscular Dystrophy, X Linked", "X-linked Emery-Dreifuss muscular dystrophy 1", "Muscular Dystrophy, Emery-Dreifuss, X-Linked", "SCAPULOPERONEAL SYNDROME, X-LINKED, FORMERLY", "scapuloperoneal syndrome, X-linked, formerly", "Emery Dreifuss Muscular Dystrophy 1, X Linked", "EMERY-Dreifuss muscular dystrophy 1, X-linked", "Emery-Dreifuss Muscular Dystrophy 1, X-Linked", "EMERY-DREIFUSS MUSCULAR DYSTROPHY 1, X-LINKED", "Emery-Dreifuss muscular dystrophy 1, X-linked", "Humeroperoneal neuromuscular disease, formerly", "HUMEROPERONEAL NEUROMUSCULAR DISEASE, FORMERLY", "Emery-Dreifuss muscular dystrophy 1 (diagnosis)", "X-linked Emery-Dreifuss muscular dystrophy (disorder)", "Benign Scapuloperoneal Muscular Dystrophy with Early Contractures", "muscular dystrophy, tardive Emery-Dreifuss type, with contractures", "Muscular dystrophy, tardive Emery-Dreifuss type, with contractures", "muscular dystrophy, tardive, Dreifuss-Emery type, with contractures", "Muscular dystrophy, tardive, Dreifuss-Emery type, with contractures", "MUSCULAR DYSTROPHY, TARDIVE, DREIFUSS-EMERY TYPE, WITH CONTRACTURES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked Emery-Dreifuss muscular dystrophy", "shortest_name_length": 4}
{"curie": "UMLS:C0270406", "names": ["Subchronic residual schizophrenia", "subchronic residual schizophrenia", "Residual Subchronic Schizophrenia", "residual subchronic schizophrenia", "Residual schizophrenia, subchronic state", "Subchronic residual schizophrenia (disorder)", "subchronic residual schizophrenia (diagnosis)", "Schizophrenic disorders, residual type, subchronic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subchronic residual schizophrenia", "shortest_name_length": 33}
{"curie": "MONDO:0007458", "names": ["ulnar drift, hereditary", "digitotalar dysmorphism", "digitotalar dysmorphism; ulnar drift, hereditary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "digitotalar dysmorphism; ulnar drift, hereditary", "shortest_name_length": 23}
{"curie": "UMLS:C0029734", "names": ["Other scleritis", "Other scleritis and episcleritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Other scleritis and episcleritis", "shortest_name_length": 15}
{"curie": "UMLS:C0220655", "names": ["pericardial effusion malignant", "Malignant pericardial effusion", "Pericardial effusion malignant", "malignant pericardial effusion", "Malignant Pericardial Effusion", "pericardial effusion, malignant", "malignant pericardial effusion (diagnosis)", "pericardial effusion due to malignant neoplasm of pericardium", "pericardial effusion due to malignant neoplasm of pericardium (diagnosis)", "Pericardial effusion co-occurrent and due to malignant neoplasm of pericardium", "Pericardial effusion co-occurrent and due to malignant neoplasm of pericardium (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant pericardial effusion", "shortest_name_length": 30}
{"curie": "UMLS:C1333452", "names": ["Esophagus Hodgkin Lymphoma", "Esophagus Hodgkin's Disease", "Esophageal Hodgkin Lymphoma", "Esophagus Hodgkin's Lymphoma", "Esophageal Hodgkin's Disease", "Esophageal Hodgkin's Lymphoma", "Hodgkin's Disease of Esophagus", "Hodgkin's Lymphoma of Esophagus", "Hodgkin's Disease of the Esophagus", "Hodgkin's Lymphoma of the Esophagus", "Primary Esophageal Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Hodgkin Lymphoma", "shortest_name_length": 26}
{"curie": "MONDO:0017303", "names": ["qualitative or quantitative defects of tropomyosin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of tropomyosin", "shortest_name_length": 50}
{"curie": "MONDO:0011455", "names": ["Lissencephaly, Familial, with Cleft Palate and Cerebellar Hypoplasia", "LISSENCEPHALY, FAMILIAL, WITH CLEFT PALATE AND CEREBELLAR HYPOPLASIA", "lissencephaly, familial, with cleft palate and cerebellar hypoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lissencephaly, familial, with cleft palate and cerebellar hypoplasia", "shortest_name_length": 68}
{"curie": "NCIT:C34865", "names": ["Optical Illusion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Optical Illusion", "shortest_name_length": 16}
{"curie": "UMLS:C0751357", "names": ["Focal Myositis", "Focal myositis", "Myositis, Focal", "Focal Myositides", "Myositides, Focal", "Focal nodular myositis", "Focal myositis (disorder)", "Inflammatory pseudotumor of skeletal muscle"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myositis, Focal", "shortest_name_length": 14}
{"curie": "UMLS:C4687641", "names": ["Heart Yolk Sac Tumor", "Cardiac Yolk Sac Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiac Yolk Sac Tumor", "shortest_name_length": 20}
{"curie": "UMLS:C0431126", "names": ["SCN", "Solitary Circumscribed Neuroma", "Palisaded Encapsulated Neuroma", "Palisaded encapsulated neuroma", "Solitary circumscribed neuroma", "Palisaded encapsulated neuroma (disorder)", "Solitary circumscribed neuroma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Palisaded encapsulated neuroma", "shortest_name_length": 3}
{"curie": "UMLS:C4763394", "names": ["Refractory PVRL DLBCL", "Refractory Primary Vitreoretinal Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Primary Vitreoretinal Diffuse Large B-Cell Lymphoma", "shortest_name_length": 21}
{"curie": "MONDO:0004582", "names": ["Rheumatic myocarditis", "Myocarditis rheumatic", "rheumatic myocarditis", "rheumatic; myocarditis", "rheumatoid myocarditis", "Rheumatoid myocarditis", "Myocarditis, rheumatic", "myocarditis; rheumatic", "acute rheumatic carditis", "Acute Rheumatic Myocarditis", "Acute rheumatic myocarditis", "Myocarditis;rheumatic;acute", "acute rheumatic myocarditis", "myocarditis; rheumatic fever", "acute; myocarditis, rheumatic", "Rheumatic fever with myocarditis", "rheumatic fever with myocarditis", "Rheumatoid myocarditis (disorder)", "rheumatic degeneration of myocardium", "Rheumatic degeneration of myocardium", "Acute Rheumatic fever with myocarditis", "Acute rheumatic fever with myocarditis", "myocarditis; rheumatic, active or acute", "rheumatic; myocarditis, active or acute", "active rheumatic fever with myocarditis", "acute rheumatic myocarditis (diagnosis)", "Active Rheumatic fever with myocarditis", "Active rheumatic fever with myocarditis", "myocarditis; rheumatic fever, active or acute", "rheumatic fever; myocarditis, active or acute", "Acute rheumatic fever with myocarditis (disorder)", "acute rheumatic myocarditis (disorder) [ambiguous]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rheumatic myocarditis", "shortest_name_length": 21}
{"curie": "UMLS:C5204622", "names": ["Bladder Neurofibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder Neurofibroma", "shortest_name_length": 20}
{"curie": "MONDO:0003143", "names": ["angiokeratoma", "Angiokeratoma", "angiokeratomas", "Angiokeratomas", "Angiokeratoma NOS", "skin angiokeratoma", "Skin Angiokeratoma", "Skin Angiokeratoma(s)", "angiokeratoma of skin", "Angiokeratoma of Skin", "Angiokeratoma of skin", "Cutaneous Angiokeratoma", "cutaneous angiokeratoma", "Angiokeratoma of the Skin", "angiokeratoma of the skin", "Angiokeratoma of skin (disorder)", "angiokeratoma (morphologic abnormality)", "Angiokeratoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angiokeratoma", "shortest_name_length": 13}
{"curie": "MONDO:0800154", "names": ["inborn disorder of the metabolism of sulfur-containing amino acids and hydrogen sulfide"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of the metabolism of sulfur-containing amino acids and hydrogen sulfide", "shortest_name_length": 87}
{"curie": "MONDO:0700185", "names": ["Feline Melanoma", "feline melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "feline melanoma", "shortest_name_length": 15}
{"curie": "MONDO:0004697", "names": ["Esophagus Leukoplakia", "esophagus leukoplakia", "Esophageal leukoplakia", "Leukoplakia esophageal", "leukoplakia; esophagus", "esophagus; leukoplakia", "Esophageal Leukoplakia", "esophageal leukoplakia", "Leukoplakia oesophageal", "Oesophageal leukoplakia", "leukoplakia of esophagus", "Leukoplakia of Esophagus", "Leucoplakia of esophagus", "Leukoplakia of esophagus", "Leukoplakia of oesophagus", "Leucoplakia of oesophagus", "Leukoplakia of the Esophagus", "leukoplakia of the esophagus", "esophageal epidermoid metaplasia", "Esophageal epidermoid metaplasia", "esophageal leukoplakia (disease)", "Esophageal Epidermoid Metaplasia", "esophageal leukoplakia (diagnosis)", "Leukoplakia of esophagus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophageal leukoplakia", "shortest_name_length": 21}
{"curie": "MONDO:0033558", "names": ["AIIDE", "Atopic Dermatitis, Enteritis, Colitis, and Eosinophilia", "ATOPIC DERMATITIS, ENTERITIS, COLITIS, AND EOSINOPHILIA", "autoinflammation, immune dysregulation, and eosinophilia", "AUTOINFLAMMATION, IMMUNE DYSREGULATION, AND EOSINOPHILIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoinflammation, immune dysregulation, and eosinophilia", "shortest_name_length": 5}
{"curie": "UMLS:C4054279", "names": ["P2 Hydronephrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "P2 Hydronephrosis", "shortest_name_length": 17}
{"curie": "MONDO:0016542", "names": ["IL10-related early-onset IBD", "autosomal recessive early-onset IBD", "IL10-related early-onset inflammatory bowel disease", "autosomal recessive early-onset inflammatory bowel disease", "immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections syndrome", "shortest_name_length": 28}
{"curie": "UMLS:C1334626", "names": ["Malignant Sertoli Cell Tumor of Testis", "Malignant Testicular Sertoli Cell Tumor", "Malignant Sertoli Cell Neoplasm of Testis", "Malignant Sertoli Cell Tumor of the Testis", "Malignant Testicular Sertoli Cell Neoplasm", "Malignant Sertoli Cell Neoplasm of the Testis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Testicular Sertoli Cell Tumor", "shortest_name_length": 38}
{"curie": "UMLS:C2910230", "names": ["cecoureterocele", "Cecoureterocele", "Cecoureterocele (disorder)", "cecoureterocele (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cecoureterocele", "shortest_name_length": 15}
{"curie": "UMLS:C1334230", "names": ["Intestinal Metaplasia of Esophageal Mucosa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal Metaplasia of Esophageal Mucosa", "shortest_name_length": 42}
{"curie": "UMLS:C2984073", "names": ["Cervical Cancer by AJCC v7 Stage", "Cervical Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Cancer by AJCC v7 Stage", "shortest_name_length": 32}
{"curie": "UMLS:C0684833", "names": ["Metastases to chest wall", "Metastasis to the Chest Wall", "Cancer metastatic to chest wall", "Metastatic Tumor to the Chest Wall", "Metastatic Neoplasm to the Chest Wall", "Secondary malignant neoplasm of chest wall", "Metastatic malignant neoplasm to chest wall", "Metastatic malignant neoplasm of chest wall", "Secondary Malignant Tumor to the Chest Wall", "Secondary Malignant Neoplasm to the Chest Wall", "Secondary malignant neoplasm of chest wall, NOS", "Metastatic Malignant Neoplasm to the Chest Wall", "Metastatic Malignant Neoplasm in the Chest Wall", "Metastatic malignant neoplasm to chest wall, NOS", "Secondary malignant neoplasm of chest wall (diagnosis)", "Metastatic malignant neoplasm to chest wall (disorder)", "malignant neoplasm of ill-defined site chest wall secondary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to chest wall", "shortest_name_length": 24}
{"curie": "UMLS:C0345468", "names": ["organ transplant rejection", "organ rejection transplants", "transplanted organ rejection", "Transplanted organ rejection", "organs rejection transplanted", "Transplanted organ rejection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transplanted organ rejection", "shortest_name_length": 26}
{"curie": "UMLS:C0278586", "names": ["Metastatic Ewing Sarcoma", "Metastatic Ewing's Sarcoma", "Ewing's sarcoma metastatic", "metastatic Ewing's sarcoma", "Ewing's Sarcoma, Metastatic", "Ewing's sarcoma, metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Ewing's Sarcoma", "shortest_name_length": 24}
{"curie": "MONDO:0005804", "names": ["HPRL", "Prolactin excess", "HYPERPROLACTINEMIA", "Hyperprolactinemia", "hyperprolactinemia", "hyperprolactinemias", "Hyperprolactinemias", "HYPERPROLACTINAEMIA", "hyperprolactinaemia", "Hyperprolactinaemia", "Hyperprolactinemia, NOS", "Hyperprolactinaemia, NOS", "hyperprolactinemia (disease)", "Hyperprolactinemia (disorder)", "hyperprolactinemia (diagnosis)", "Prolactin Hypersecretion Syndrome", "inappropriate prolactin secretion", "prolactin hypersecretion syndrome", "inappropriate secretion prolactin", "Inappropriate Prolactin Secretion", "Inappropriate Secretion Prolactin", "prolactin secretion, inappropriate", "Prolactin Secretion, Inappropriate", "Hypersecretion Syndrome, Prolactin", "Secretion, Inappropriate Prolactin", "Syndrome, Prolactin Hypersecretion", "syndrome, prolactin hypersecretion", "prolactin, inappropriate secretion", "secretion, inappropriate prolactin", "hypersecretion syndrome, prolactin", "Prolactin, Inappropriate Secretion", "secretion prolactin, inappropriate", "Secretion Prolactin, Inappropriate", "inappropriate prolactin secretion syndrome", "Inappropriate Prolactin Secretion Syndrome", "Increased circulating prolactin concentration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperprolactinemia", "shortest_name_length": 4}
{"curie": "UMLS:C0278736", "names": ["Stage II Lymphoblastic Lymphoma", "NHL, lymphoblastic stage II childhood", "Stage II Childhood Lymphoblastic Lymphoma", "Pediatric Lymphoblastic Lymphoma Stage II", "stage II lymphoblastic childhood lymphoma", "stage II childhood lymphoblastic lymphoma", "Childhood Lymphoblastic Lymphoma Stage II", "Stage II Pediatric Lymphoblastic Lymphoma", "Ann Arbor Stage II Childhood Lymphoblastic Lymphoma", "Stage II Childhood Precursor Lymphoblastic Lymphoma", "pediatric lymphoblastic non-Hodgkin's lymphoma, stage II", "lymphoblastic stage II non-Hodgkin's lymphoma, childhood", "childhood non-Hodgkin's lymphoma, lymphoblastic stage II", "non-Hodgkin's lymphoma, lymphoblastic stage II childhood", "lymphoma, non-Hodgkin's, lymphoblastic stage II childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Childhood Lymphoblastic Lymphoma", "shortest_name_length": 31}
{"curie": "UMLS:C2981611", "names": ["Stage IIA Digestive System Neuroendocrine Tumor", "Stage IIA Digestive System Neuroendocrine Neoplasm", "Stage IIA Gastrointestinal Neuroendocrine Neoplasm", "Stage IIA Digestive System Neuroendocrine Tumor AJCC v7", "Stage IIA Digestive System Neuroendocrine Neoplasm AJCC v7", "Stage IIA Gastrointestinal Neuroendocrine Neoplasm AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Digestive System Neuroendocrine Tumor AJCC v7", "shortest_name_length": 47}
{"curie": "MONDO:0800033", "names": ["MTTQ MELAS syndrome", "MELAS syndrome caused by mutation in MTTQ"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MELAS syndrome caused by mutation in MTTQ", "shortest_name_length": 19}
{"curie": "MONDO:0007001", "names": ["Tricuspid valve prolapse", "Tricuspid Valve Prolapse", "tricuspid valve prolapse", "Tricuspid Valve Prolapses", "Valve Prolapse, Tricuspid", "Prolapse, Tricuspid Valve", "Prolapses, Tricuspid Valve", "Valve Prolapses, Tricuspid", "TVP - Tricuspid valve prolapse", "tricuspid valve prolapse (disease)", "Tricuspid valve prolapse (disorder)", "tricuspid valve prolapse (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tricuspid valve prolapse", "shortest_name_length": 24}
{"curie": "MONDO:0010206", "names": ["LAH3", "Lah3", "Hypt8", "ARWH1", "HYPT8", "HYPOTRICHOSIS 8", "hypotrichosis 8", "LPAR6 hypotrichosis", "hypotrichosis type 8", "hypotrichosis caused by mutation in LPAR6", "hypotrichosis, localized, autosomal recessive 3", "HYPOTRICHOSIS, LOCALIZED, AUTOSOMAL RECESSIVE 3", "Hypotrichosis, Localized, Autosomal Recessive, 3", "woolly hair, autosomal recessive 1, with or without hypotrichosis", "WOOLLY HAIR, AUTOSOMAL RECESSIVE 1, WITH OR WITHOUT HYPOTRICHOSIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotrichosis 8", "shortest_name_length": 4}
{"curie": "MONDO:0000502", "names": ["Villous adenoma", "ADENOMA VILLOUS", "villous adenoma", "adenoma villous", "VILLOUS ADENOMA", "Villous Adenoma", "Villous Adenomas", "Adenoma, Villous", "villous adenomas", "Villous papilloma", "Adenomas, Villous", "Villous adenoma NOS", "Villous adenoma, NOS", "GI Tract Villous Adenoma", "Gastrointestinal Tract Villous Adenoma", "Villous adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "villous adenoma", "shortest_name_length": 15}
{"curie": "MONDO:0007316", "names": ["Cm1", "CM1", "Arnold Chiari type 1", "Chiari I malformation", "CM1 with Syringomyelia", "CM1 WITH SYRINGOMYELIA", "Cm1 with syringomyelia", "Chiari Malformation Type I", "Chiari malformation type I", "Chiari type I malformation", "CHIARI MALFORMATION TYPE I", "chiari type i malformation", "Chiari malformation type 1", "type I Chiari malformation", "chiari malformation type i", "Type I Chiari malformation", "Type 1 Chiari malformation", "Chiari malformation, type I", "Chiari malformation, type 1", "Arnold-Chiari type I malformation", "Type I Arnold Chiari Malformation", "Arnold Chiari type I malformation", "Arnold-Chiari malformation type 1", "Arnold-Chiari malformation type I", "Type I Arnold-Chiari Malformation", "type I Arnold-Chiari malformation", "Arnold Chiari Malformation, Type 1", "Arnold Chiari Malformation, Type I", "Arnold-Chiari Malformation, Type 1", "Arnold-Chiari Malformation, Type I", "Chiari malformation type I (disorder)", "type I Chiari malformation (diagnosis)", "Chiari malformation type 1 with syringomyelia", "CHIARI MALFORMATION TYPE I WITH SYRINGOMYELIA", "Chiari Malformation Type I with Syringomyelia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chiari malformation type I", "shortest_name_length": 3}
{"curie": "MONDO:0004845", "names": ["Aphtha", "aphtha", "oral ulcer", "canker sore", "Canker sore", "Oral aphthae", "oral aphthae", "oral aphthous ulcer", "aphthous ulceration", "Oral aphthous ulcer", "Aphthous ulceration", "aphthous stomatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aphthous stomatitis", "shortest_name_length": 6}
{"curie": "MONDO:0021309", "names": ["endocervix cancer", "cancer of endocervix", "Cancer of endocervix", "Malignant Endocervix Tumor", "malignant endocervix tumor", "Malignant Endocervical Tumor", "malignant endocervical tumor", "malignant tumor of endocervix", "malignant endocervix neoplasm", "Malignant Endocervix Neoplasm", "Malignant Tumor of Endocervix", "Malignant Endocervical Neoplasm", "malignant endocervical neoplasm", "malignant neoplasm of endocervix", "Malignant neoplasm of endocervix", "Malignant Neoplasm of Endocervix", "malignant tumor of cervical canal", "Malignant Tumor of the Endocervix", "malignant tumor of the endocervix", "Malignant Uterine Endocervix Tumor", "malignant uterine endocervix tumor", "Malignant Neoplasm of the Endocervix", "malignant neoplasm of the endocervix", "malignant neoplasm of cervical canal", "malignant tumor of endocervical canal", "malignant uterine endocervix neoplasm", "Malignant Tumor of Uterine Endocervix", "Malignant Uterine Endocervix Neoplasm", "malignant tumor of uterine endocervix", "cervical neoplasm malignant endocervix", "Malignant neoplasm of cervical canal NOS", "malignant neoplasm of endocervical canal", "Malignant neoplasm of endocervical canal", "malignant neoplasm of uterine endocervix", "Malignant Neoplasm of Uterine Endocervix", "malignant tumor of the uterine endocervix", "Malignant Tumor of the Uterine Endocervix", "Malignant neoplasm of endocervix (disorder)", "Malignant Neoplasm of the Uterine Endocervix", "malignant neoplasm of the uterine endocervix", "malignant neoplasm of endocervix (diagnosis)", "malignant neoplasm of cervical canal (diagnosis)", "Malignant neoplasm of endocervical canal (disorder)", "malignant neoplasm of endocervical canal (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant neoplasm of endocervix", "shortest_name_length": 17}
{"curie": "MONDO:0021545", "names": ["myoblastoma", "Muscle Tumor", "muscle tumor", "myoblastomas", "muscle tumors", "muscle tumours", "Muscular tumor", "muscles tumors", "Muscle neoplasm", "Tumor of muscle", "tumor of muscle", "Tumor of Muscle", "muscle neoplasm", "Myomatous tumor", "myomatous tumor", "Muscles--Tumors", "Muscle Neoplasm", "Myomatous Tumor", "myofibroblastoma", "Tumour of muscle", "Neoplasm, Muscle", "Muscle Neoplasms", "Myomatous tumour", "myofibroblastomas", "Neoplasms, Muscle", "neoplasm of muscle", "Myomatous neoplasm", "myomatous neoplasm", "Neoplasm of muscle", "Neoplasm of Muscle", "Myomatous Neoplasm", "tumor of the muscle", "MYOMATOUS NEOPLASMS", "Tumor of the Muscle", "Myomatous Neoplasms", "Neoplasm of the Muscle", "muscle tissue neoplasm", "Muscle Tissue Neoplasm", "neoplasm of the muscle", "Muscle Tissue Neoplasms", "neoplasm, muscle tissue", "Neoplasm, Muscle Tissue", "muscle tissue neoplasms", "Neoplasms, Muscle Tissue", "Neoplasm of muscle (disorder)", "neoplasm of muscle (diagnosis)", "Soft tissue tumor of muscle differentiation", "Soft tissue tumour of muscle differentiation", "Myomatous neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myomatous neoplasm", "shortest_name_length": 11}
{"curie": "MONDO:0020705", "names": ["NTD", "spina bifida", "neural tube defects", "spina bifida, susceptibility to", "NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO", "neural tube defects, SUSCEPTIBILITY to", "neural tube defects, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neural tube defects, susceptibility to", "shortest_name_length": 3}
{"curie": "MONDO:0015677", "names": ["cardiac diverticulum", "Cardiac diverticulum", "cardiac diverticulum (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiac diverticulum", "shortest_name_length": 20}
{"curie": "MONDO:0033649", "names": ["MC4DN14", "mitochondrial complex 4 deficiency, nuclear type 14", "MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 14", "mitochondrial complex IV deficiency, nuclear type 14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 4 deficiency, nuclear type 14", "shortest_name_length": 7}
{"curie": "MONDO:0020508", "names": ["Primary syringomyelia", "primary syringomyelia", "congenital syringomyelia", "Congenital syringomyelia", "Congenital syringomyelia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary syringomyelia", "shortest_name_length": 21}
{"curie": "UMLS:C1266154", "names": ["Borderline Ovarian Mucinous Adenofibroma", "Mucinous adenofibroma of borderline malignancy", "Mucinous cystadenofibroma of borderline malignancy", "Ovarian Mucinous Adenofibroma of Borderline Malignancy", "Mucinous adenofibroma of borderline malignancy (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mucinous adenofibroma of borderline malignancy", "shortest_name_length": 40}
{"curie": "UMLS:C0085920", "names": ["Brachial Neuralgia", "brachial neuralgia", "Brachial neuralgia", "Brachial Neuralgias", "Neuralgia, Brachial", "Neuralgias, Brachial", "Brachial plexus neuralgia", "Brachial plexus neuralgia (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brachial Neuralgia", "shortest_name_length": 18}
{"curie": "UMLS:C1511286", "names": ["Breast Burkitt Lymphoma", "Breast Burkitt's Lymphoma", "Burkitt's lymphoma of breast", "Burkitt's lymphoma of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Burkitt's lymphoma of breast", "shortest_name_length": 23}
{"curie": "MONDO:0011242", "names": ["BSND", "BARTS4A", "BSND Bartter syndrome", "Bartter disease type 4A", "Bartter disease type 4a", "Bartter syndrome type 4a", "Bartter syndrome, type 4A", "Bartter Syndrome, Type 4A", "BARTTER SYNDROME, TYPE 4A", "Bartter syndrome type 4a (disorder)", "Bartter syndrome type 4a (diagnosis)", "Bartter syndrome caused by mutation in BSND", "sensorineural deafness with mild renal dysfunction", "Sensorineural Deafness With Mild Renal Dysfunction", "SENSORINEURAL DEAFNESS WITH MILD RENAL DYSFUNCTION", "neonatal Bartter syndrome with sensorineural deafness", "BARTTER SYNDROME, NEONATAL, WITH SENSORINEURAL DEAFNESS", "Bartter syndrome, neonatal, with sensorineural deafness", "Bartter syndrome, infantile, with sensorineural deafness", "BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS", "Bartter syndrome, type 4A, neonatal, with sensorineural deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bartter disease type 4A", "shortest_name_length": 4}
{"curie": "MONDO:0020391", "names": ["hemitruncus arteriosus", "pulmonary artery coming from the aorta", "abnormal origin of right or left pulmonary artery from the aorta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary artery coming from the aorta", "shortest_name_length": 22}
{"curie": "UMLS:C1270206", "names": ["Desmoplastic Mesothelioma", "Desmoplastic mesothelioma", "Desmoplastic mesothelioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Desmoplastic mesothelioma", "shortest_name_length": 25}
{"curie": "MONDO:0019318", "names": ["ILVEN", "Dermatitic epidermal nevus", "Dermatitic epidermal naevus", "linear verrucose epidermal nevus", "Inflammatory linear verrucous epidermal nevus", "Inflammatory Linear Verrucose Epidermal Nevus", "inflammatory linear verrucous epidermal nevus", "Inflammatory Linear Verrucous Epidermal Naevus", "Inflammatory linear verrucous epidermal naevus", "inflammatory linear verrucous epidermal naevus", "ILVEN - Inflammatory linear verrucous epidermal nevus", "ILVEN - Inflammatory linear verrucous epidermal naevus", "Inflammatory linear verrucous epidermal nevus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory linear verrucous epidermal nevus", "shortest_name_length": 5}
{"curie": "MONDO:0018846", "names": ["Aphalia", "Aphallia", "Aphallus", "Micropenis", "micropenis", "Absent penis", "Penis aplasia", "penis; absent", "aplasia; penis", "Penis agenesis", "penis agenesia", "penis; aplasia", "Penis agenesia", "penis agenesis", "absence; penis", "Penile agenesis", "agenesis; penis", "penis; agenesis", "penile agenesis", "Penile Agenesis", "Aplasia of penis", "Aplasia of the penis", "Agenesis of the penis", "agenesis of the penis", "Aplasia of penis (disorder)", "Congenital absence of penis", "Congenital Absence of Penis", "congenital absence of penis", "Congenital absence or aplasia of penis", "Congenital absence of penis (disorder)", "congenital absence and aplasia of penis", "Congenital absence and aplasia of penis", "congenital absence and aplasia of penis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "penile agenesis", "shortest_name_length": 7}
{"curie": "MONDO:0008716", "names": ["Metageria", "Acrogeria", "ACROGERIA", "METAGERIA", "acrogeria", "Acrometageria", "ACROMETAGERIA", "acrometageria", "Gottron syndrome", "familial acrogeria", "Gottron's syndrome", "Acrogeria (disorder)", "Metageria (disorder)", "ACROGERIA, GOTTRON TYPE", "Acrogeria, Gottron type", "Acrogeria, gottron type", "acrogeria, Gottron type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acrogeria", "shortest_name_length": 9}
{"curie": "UMLS:C0751670", "names": ["SCA3, Machado type", "Machado-Joseph disease type 3", "Type III Machado Joseph Disease", "Machado-Joseph Disease Type III", "Machado Joseph Disease Type III", "Type III Machado-Joseph Disease", "Spinocerebellar ataxia type 3, Machado type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Machado-Joseph Disease Type III", "shortest_name_length": 18}
{"curie": "MONDO:0033047", "names": ["PRLTS6", "Perrault syndrome 6", "PERRAULT SYNDROME 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perrault syndrome 6", "shortest_name_length": 6}
{"curie": "UMLS:C0339512", "names": ["bull's eye macular dystrophy", "Bull's eye macular dystrophy", "Bull's eye macular dystrophy (disorder)", "bull's eye macular dystrophy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bull's eye macular dystrophy", "shortest_name_length": 28}
{"curie": "MONDO:0020519", "names": ["Schüller-Christian", "Hand-Schüller-Christian", "Chronic histiocytosis X", "Schuller-Christian syndrome", "SCHUELLER-CHRISTIAN DISEASE", "Schüller-Christian syndrome", "schuller christian syndrome", "Langerhan's cell histiocytosis", "hand-SChüller-Christian disease", "Hand-Schüller-Christian disease", "hand-Schuller-Christian disease", "hand-schuller-christian disease", "hand schuller christian disease", "hand christian schuller disease", "Hand Schuller Christian disease", "disease hand schuller christian", "Hand-Schüller-Christian Disease", "christian disease hand schuller", "Hand-Schuller-Christian Disease", "Hand-Schuller-Christian disease", "Hand-Schueller-Christian disease", "Chronic idiopathic xanthomatosis", "christian diseases hand schuller", "hand-schueller-christian disease", "multifocal eosinophilic granuloma", "Hand-Schueller-Christian syndrome", "HAND-SCHUELLER-CHRISTIAN SYNDROME", "Generalized histiocytosis of bones", "Generalised histiocytosis of bones", "Chronic disseminated histiocytosis X", "Systemic reticuloendothelial granuloma", "Langerhans cell histiocytosis, multifocal", "Hand-Schüller-Christian disease (disorder)", "multifocal eosinophilic granuloma (diagnosis)", "classic multifocal Langerhans cell histiocytosis", "Chronic differentiated progressive histiocytosis", "chronic multifocal Langerhans cell histiocytosis", "Classic Multifocal Langerhans Cell Histiocytosis", "multifocal Unisystem Langerhans cell histiocytosis", "Multifocal Unisystem Langerhans Cell Histiocytosis", "Multifocal and unisystemic Langerhans cell histiocytosis", "Langerhans cell histiocytosis, multifocal (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hand-Schuller-Christian disease", "shortest_name_length": 18}
{"curie": "MONDO:0006304", "names": ["minor salivary gland adenocarcinoma", "Minor Salivary Gland Adenocarcinoma", "Adenocarcinoma of Minor Salivary Gland", "adenocarcinoma of minor salivary gland", "adenocarcinoma of the minor salivary gland", "Adenocarcinoma of the Minor Salivary Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "minor salivary gland adenocarcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C0008301", "names": ["choke", "choked", "CHOKING", "Choking", "choking", "Choking (finding)", "choking (symptom)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Choking", "shortest_name_length": 5}
{"curie": "UMLS:C2348726", "names": ["Pleomorphic Spindle and Giant Cell Carcinoma of Gallbladder", "Pleomorphic Spindle and Giant Cell Carcinoma of the Gallbladder", "Gallbladder Undifferentiated Carcinoma, Spindle and Giant Cell Type", "Undifferentiated Gallbladder Carcinoma, Spindle and Giant Cell Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gallbladder Undifferentiated Carcinoma, Spindle and Giant Cell Type", "shortest_name_length": 59}
{"curie": "MONDO:0018596", "names": ["systemic PAN", "systemic periarteritis nodosa", "systemic polyarteritis nodosa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "systemic polyarteritis nodosa", "shortest_name_length": 12}
{"curie": "UMLS:C3495489", "names": ["Rieger anomaly", "Rieger's anomaly", "Mesodermal iris dysgenesis", "Irido-trabecular dysgenesis", "Mesodermal dysgenesis of iris", "Imperforate pectinate glaucoma", "Rieger eye malformation sequence", "Irido-trabecular dysgenesis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rieger eye malformation sequence", "shortest_name_length": 14}
{"curie": "UMLS:C4053713", "names": ["Childhood Malignant Fibrous Histiocytoma of Bone", "Undifferentiated High Grade Pleomorphic Sarcoma of Bone", "Childhood Undifferentiated High Grade Pleomorphic Sarcoma", "Childhood Undifferentiated High Grade Pleomorphic Sarcoma of Bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Undifferentiated High Grade Pleomorphic Sarcoma of Bone", "shortest_name_length": 48}
{"curie": "MONDO:0009932", "names": ["pulmonary bullae causing pneumothorax", "PULMONARY BULLAE CAUSING PNEUMOTHORAX", "Pulmonary Bullae Causing Pneumothorax"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary bullae causing pneumothorax", "shortest_name_length": 37}
{"curie": "MONDO:0025511", "names": ["genetic neuroendocrine tumor", "inherited neuroendocrine tumor", "hereditary neuroendocrine neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited neuroendocrine tumor", "shortest_name_length": 28}
{"curie": "UMLS:C4525342", "names": ["Hilar Cholangiocarcinoma by AJCC v7 Stage", "Perihilar Cholangiocarcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hilar Cholangiocarcinoma by AJCC v7 Stage", "shortest_name_length": 41}
{"curie": "MONDO:0009703", "names": ["LSMFLAD", "lipid storage myopathy", "myopathy with abnormal lipid metabolism", "Myopathy with Abnormal Lipid Metabolism", "LIPID storage myopathy due to flavin adenine dinucleotide synthetase deficiency", "lipid storage myopathy due to flavin adenine dinucleotide synthetase deficiency", "LIPID STORAGE MYOPATHY DUE TO FLAVIN ADENINE DINUCLEOTIDE SYNTHETASE DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy with abnormal lipid metabolism", "shortest_name_length": 7}
{"curie": "UMLS:C4725599", "names": ["Distal Esophagus Squamous Cell Carcinoma", "Squamous Cell Carcinoma of the Distal Esophagus", "Squamous Cell Carcinoma of the Lower Third of the Esophagus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Distal Esophagus Squamous Cell Carcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0000926", "names": ["ACCOMMODATION ABNORMAL", "Accommodation abnormal", "DISORDER ACCOMMODATION", "Disorder accommodation", "Accommodation disorder", "ACCOMMODATION DISORDER", "Accommodation debility", "accommodation; disorder", "disorder; accommodation", "Accommodation difficulty", "Accommodation disturbance", "Disorder of accommodation", "ACCOMMODATION DISTURBANCE", "disorder of accommodation", "eye accommodation disease", "disturbance; accommodation", "Disorders of accommodation", "Abnormality of accommodation", "ABNORMALITY OF ACCOMMODATION", "Disorder of accommodation, NOS", "Pupillary accommodation disorder", "Visual accommodation disturbance of", "Disorder of accommodation (disorder)", "disorder of accommodation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eye accommodation disease", "shortest_name_length": 22}
{"curie": "UMLS:C1514816", "names": ["Refractory High Grade Burkitt-Like Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory High Grade Burkitt-Like Lymphoma", "shortest_name_length": 43}
{"curie": "MONDO:0007336", "names": ["CP", "CPI", "CLEFT PALATE", "cleft palate", "dominant cleft palate", "isolated cleft palate", "CLEFT PALATE, ISOLATED", "cleft palate, isolated", "Cleft Palate, Isolated", "Cleft palate, isolated", "nonsyndromic cleft palate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated cleft palate", "shortest_name_length": 2}
{"curie": "UMLS:C0862636", "names": ["Metastatic Prostate Adenocarcinoma", "Metastatic Prostatic Adenocarcinoma", "Adenocarcinoma of the prostate metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma of the prostate metastatic", "shortest_name_length": 34}
{"curie": "MONDO:0700090", "names": ["ETL1", "Epilepsy, Familial Temporal Lobe 1", "epilepsy, familial temporal lobe, 1", "EPILEPSY, FAMILIAL TEMPORAL LOBE, 1", "epilepsy, familial temporal lobe, type 1", "epilepsy, partial, with auditory features", "Autosomal Dominant Lateral Temporal Lobe Epilepsy", "epilepsy, lateral temporal lobe, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, familial temporal lobe, 1", "shortest_name_length": 4}
{"curie": "MONDO:0001692", "names": ["Pederasty", "pederosis", "Pedophilia", "pedophilia", "Paedophilia", "paedophilia", "Pedophilias", "Pederasties", "paedophilias", "Pedophilia, NOS", "Paedophilia, NOS", "Pedophilia (disorder)", "pedophilia (diagnosis)", "deviation; sexual, pedophilia", "sexual; deviation, pedophilia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pedophilia", "shortest_name_length": 9}
{"curie": "MONDO:0009008", "names": ["CHDTHP", "Orstavik Lindemann Solberg syndrome", "Ostravik-Lindemann-Solberg syndrome", "Ostravik lindemann solberg syndrome", "Ostravik Lindemann Solberg syndrome", "heart defect, tongue hamartoma and polysyndactyly", "Heart defect, tongue hamartoma and polysyndactyly", "Heart defect-tongue hamartoma-polysyndactyly syndrome", "heart defect-tongue hamartoma-polysyndactyly syndrome", "Heart defect, tongue hamartoma, polysyndactyly syndrome", "heart defect - tongue hamartoma - polysyndactyly syndrome", "CONGENITAL HEART DEFECTS, HAMARTOMAS OF TONGUE, AND POLYSYNDACTYLY", "Congenital heart defects, hamartomas of tongue, and polysyndactyly", "congenital heart defects, hamartomas of tongue, and polysyndactyly", "Heart defect, tongue hamartoma, polysyndactyly syndrome (disorder)", "CONGENITAL HEART DEFECTS, HAMARTOMAS OF THE TONGUE, AND POLYSYNDACTYLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heart defect - tongue hamartoma - polysyndactyly syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C1335523", "names": ["Atypical Adenomatous Prostate Hyperplasia", "Prostatic Atypical Adenomatous Hyperplasia", "Atypical Adenomatous Hyperplasia (Adenosis)", "Atypical Adenomatous Hyperplasia of Prostate", "Atypical Adenomatous Hyperplasia of the Prostate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostatic Atypical Adenomatous Hyperplasia", "shortest_name_length": 41}
{"curie": "MONDO:0012220", "names": ["GS3", "Griscelli disease type 3", "Griscelli syndrome type 3", "GRISCELLI SYNDROME, TYPE 3", "Griscelli syndrome, type 3", "Griscelli Syndrome, Type 3", "Griscelli-Pruniéras syndrome type 3", "Griscelli-Prunieras syndrome type 3", "Griscelli-Pruni��ras syndrome type 3", "Griscelli-PruniC)ras syndrome type 3", "Hypopigmentation-immunodeficiency disease type 3", "Hypopigmentation-immunodeficiency disease type 3 (disorder)", "Hypomelanosis with no immunologic or neurologic manifestations", "hypomelanosis with no immunologic or neurologic manifestations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Griscelli syndrome type 3", "shortest_name_length": 3}
{"curie": "UMLS:C0586354", "names": ["Esophageal dysplasia", "Esophageal Dysplasia", "Oesophageal dysplasia", "Esophageal dysplasia (disorder)", "Esophageal Intraepithelial Neoplasia", "Intraepithelial Neoplasia of Esophagus", "Intraepithelial Neoplasia of the Esophagus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal dysplasia", "shortest_name_length": 20}
{"curie": "UMLS:C1565951", "names": ["Sphenoid Wing Meningioma", "Sphenoid wing meningioma", "Wing Meningioma, Sphenoid", "Sphenoid Wing Meningiomas", "Meningioma, Sphenoid Wing", "Meningiomas, Sphenoid Wing", "Wing Meningiomas, Sphenoid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sphenoid Wing Meningioma", "shortest_name_length": 24}
{"curie": "UMLS:C1335496", "names": ["Primitive Neuroectodermal Tumor with Leptomeningeal Spread", "Central Nervous System Embryonal Tumor, NOS with Leptomeningeal Spread", "Central Nervous System Embryonal Tumor, Not Otherwise Specified with Leptomeningeal Spread"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Embryonal Tumor, Not Otherwise Specified with Leptomeningeal Spread", "shortest_name_length": 58}
{"curie": "MONDO:0007403", "names": ["CJD", "inherited CJD", "Inherited CJD", "Creutzfeldt-Jakob disease", "Familial Creutzfeldt-Jakob", "Familial Creutzfeldt-Jakob Disease", "Familial Creutzfeldt Jakob Disease", "familial Creutzfeldt-Jakob disease", "Familial Creutzfeldt-Jakob disease", "Creutzfeldt-Jakob disease, variant", "inherited Creutzfeldt-Jakob disease", "Creutzfeldt-Jakob disease, sporadic", "Disease, Familial Creutzfeldt-Jakob", "Creutzfeldt-Jakob disease, familial", "CREUTZFELDT-JAKOB DISEASE, FAMILIAL", "Familial Creutzfeldt-Jakob Diseases", "Creutzfeldt Jakob Disease, Familial", "Creutzfeldt-Jakob Disease, Familial", "Inherited Creutzfeldt-Jakob disease", "Creutzfeldt-Jakob Diseases, Familial", "hereditary Creutzfeldt Jacob disease", "Familial Creutzfeldt-Jakob (disorder)", "fCJD (Familial Creutzfeldt-Jakob disease)", "Creutzfeldt-Jakob Disease, Heidenhain Variant", "Creutzfeldt-Jakob disease, Heidenhain variant", "CREUTZFELDT-JAKOB DISEASE, HEIDENHAIN VARIANT", "familial Creutzfeldt-Jakob disease (diagnosis)", "Creutzfeldt-Jakob disease, variant, resistance to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited Creutzfeldt-Jakob disease", "shortest_name_length": 3}
{"curie": "UMLS:C0278566", "names": ["Skin T-Cell Lymphoma Stage I", "T-Cell Lymphoma of Skin Stage I", "Cutaneous T-Cell Lymphoma Stage I", "stage I cutaneous T-cell lymphoma", "Cutaneous T-cell lymphoma stage I", "cutaneous T-cell lymphoma, stage I", "T-Cell Lymphoma of the Skin Stage I", "Stage I Cutaneous T-Cell Non-Hodgkin Lymphoma", "stage I cutaneous T-cell non-Hodgkin lymphoma", "Stage I Cutaneous T-Cell Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous T-cell lymphoma stage I", "shortest_name_length": 28}
{"curie": "MONDO:0032600", "names": ["IDDMSF", "SNIBCPS", "SNIJDERS BLOK-CAMPEAU SYNDROME", "Snijders Blok-Campeau syndrome", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SPEECH DELAY, AND DYSMORPHIC FACIES", "intellectual developmental disorder with macrocephaly, speech delay, and dysmorphic facies", "CHD3-related developmental delay-speech delay-intellectual disability-abnormalities of vision-facial dysmorphism syndrome", "CHD3-related developmental delay, speech delay, intellectual disability, abnormalities of vision, facial dysmorphism syndrome", "Chromodomain helicase dna-binding protein 3- related developmental delay, speech delay, intellectual disability, abnormalities of vision, facial dysmorphism syndrome", "Chromodomain helicase dna-binding protein 3- related developmental delay, speech delay, intellectual disability, abnormalities of vision, facial dysmorphism syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Snijders Blok-Campeau syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0013259", "names": ["CSNBO2", "Oguchi disease 2", "Oguchi disease-2", "OGUCHI DISEASE 2", "GRK1 Oguchi disease", "Oguchi disease type 2", "Oguchi disease caused by mutation in GRK1", "congenital stationary night blindness Oguchi type 2", "NIGHT BLINDNESS, CONGENITAL STATIONARY, OGUCHI TYPE 2", "night blindness, congenital stationary, Oguchi type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oguchi disease-2", "shortest_name_length": 6}
{"curie": "MONDO:0017747", "names": ["disorder of fucoglycosan synthesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of fucoglycosan synthesis", "shortest_name_length": 34}
{"curie": "UMLS:C5238540", "names": ["Refractory High Risk Chronic Myelomonocytic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory High Risk Chronic Myelomonocytic Leukemia", "shortest_name_length": 52}
{"curie": "MONDO:0011056", "names": ["WT4", "FWT1", "Wilms tumor 4", "WILMS TUMOR 4", "Wilms Tumor 4", "Wilms tumor type 4", "Wilms tumor, type 4", "Familial Wilms Tumor 1", "familial Wilms tumor 1", "FAMILIAL WILMS TUMOR 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wilms tumor 4", "shortest_name_length": 3}
{"curie": "MONDO:0010842", "names": ["VMCM", "VMCM1", "Vmcm1", "Mucocutaneous Venous Malformations", "Mucocutaneous venous malformations", "cutaneomucosal venous malformation", "mucocutaneous venous malformations", "cutaneous and mucosal venous malformation", "Cutaneous and mucosal venous malformation", "Multiple cutaneous and mucosal venous malformation", "multiple cutaneous and mucosal venous malformations", "Multiple Cutaneous and Mucosal Venous Malformations", "VENOUS MALFORMATIONS, MULTIPLE CUTANEOUS AND MUCOSAL", "Venous Malformations, Multiple Cutaneous and Mucosal", "VENOUS malformations, multiple cutaneous and mucosal", "Multiple venous malformation of skin and mucous membrane", "Multiple venous malformation of skin and mucous membrane (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple cutaneous and mucosal venous malformations", "shortest_name_length": 4}
{"curie": "MONDO:0030835", "names": ["DIGFAN", "DEVELOPMENTAL DELAY, IMPAIRED GROWTH, DYSMORPHIC FACIES, AND AXONAL NEUROPATHY", "developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy", "shortest_name_length": 6}
{"curie": "UMLS:C0549429", "names": ["SURGICAL SITE REACTION", "Surgical site reaction", "Surgical site reaction (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Surgical site reaction", "shortest_name_length": 22}
{"curie": "MONDO:0008644", "names": ["VCFS", "22q11.2DS", "VCF syndrome", "VCF Syndrome", "VCF SYNDROME", "Syndrome, VCF", "Deletion 22q11.2", "Shprintzen Syndrome", "Shprintzen syndrome", "Sedlackova Syndrome", "Sedlackova syndrome", "shprintzen syndrome", "Syndrome, Shprintzen", "shprintzens syndrome", "Syndrome, Sedlackova", "velofacial hypoplasia", "22q11 deletion syndrome", "Shprintzen VCF syndrome", "Shprintzen VCF Syndrome", "SHPRINTZEN VCF SYNDROME", "Deletion 22q11.2 syndrome", "VELOCARDIOFACIAL SYNDROME", "deletion 22q11.2 syndrome", "Velocardiofacial syndrome", "Velocardiofacial Syndrome", "velocardiofacial syndrome", "22q11.2 Deletion Syndrome", "Deletion 22q11.2 Syndrome", "Syndrome, Velocardiofacial", "Deletion Syndrome, 22q11.2", "syndromes velocardiofacial", "Velo-cardio-facial syndrome", "Velo-Cardio-Facial Syndrome", "Velo Cardio Facial Syndrome", "velo-cardio-facial syndrome", "Syndrome, Velo-Cardio-Facial", "VCF-Velocardiofacial syndrome", "VCF-velocardiofacial syndrome", "22q11.2 deletion syndrome (VCFS)", "chromosome 22Q11.2 deletion syndrome", "Chromosome 22q11.2 deletion syndrome", "CHROMOSOME 22q11.2 DELETION SYNDROME", "velocardiofacial syndrome (VCF, VCFS)", "22q11.2 deletion syndrome (VCFS) (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "velocardiofacial syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0338763", "names": ["episodic cocaine dependence", "Cocaine dependence, episodic", "Cocaine dependence, episodic use", "Cocaine Dependence, Episodic Use", "episodic cocaine dependence (diagnosis)", "Cocaine dependence, episodic (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cocaine dependence, episodic", "shortest_name_length": 27}
{"curie": "MONDO:0013464", "names": ["EA5", "Episodic ataxia type 5", "episodic ataxia type 5", "Episodic Ataxia, Type 5", "episodic ataxia, type 5", "EPISODIC ATAXIA, TYPE 5", "CACNB4 hereditary episodic ataxia", "Episodic ataxia type 5 (disorder)", "hereditary episodic ataxia caused by mutation in CACNB4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "episodic ataxia type 5", "shortest_name_length": 3}
{"curie": "UMLS:C5239130", "names": ["Peritoneal Biphasic Mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peritoneal Biphasic Mesothelioma", "shortest_name_length": 32}
{"curie": "UMLS:C1519935", "names": ["Vaginal Undifferentiated Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Undifferentiated Sarcoma", "shortest_name_length": 32}
{"curie": "MONDO:0020782", "names": ["chronic gingivitis", "Chronic gingivitis", "Chronic Gingivitis", "GINGIVITIS CHRONIC", "chronic; gingivitis", "gingivitis; chronic", "Chronic gingivitis NOS", "Gingivitis (chronic) NOS", "Chronic gingivitis (disorder)", "chronic gingivitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic gingivitis", "shortest_name_length": 18}
{"curie": "MONDO:0008627", "names": ["Ureter Ca", "Ureter cancer", "Ureter Cancer", "ureter cancer", "cancer ureter", "Ureter Cancers", "Ureters--Cancer", "Ureteral cancer", "ureteral cancer", "Ureteral Cancer", "Ureteric cancer", "cancer of ureter", "Cancer of Ureter", "Cancer of ureter", "Cancer, Ureteral", "of ureter cancer", "Ureteral Cancers", "ureter, cancer of", "ureter, cancer OF", "Ureter, Cancer Of", "Cancers, Ureteral", "URETER, CANCER OF", "Ureteral Neoplasms", "Ureteric cancer NOS", "cancer of the ureter", "Cancer of the Ureter", "Neoplasm malig;ureter", "Malignant Ureter Tumor", "malignant ureter tumor", "Malignant Ureteral Tumor", "malignant ureteral tumor", "malignant tumor of ureter", "Malignant Ureter Neoplasm", "Malignant tumor of ureter", "Malignant Tumor of Ureter", "malignant ureter neoplasm", "Malignant tumour of ureter", "malignant tumour of ureter", "malignant ureteral neoplasm", "Malignant Ureteral Neoplasm", "malignant neoplasm of ureter", "Malignant neoplasm of ureter", "Malignant Neoplasm of Ureter", "malignant tumor of the ureter", "Malignant Tumor of the Ureter", "Malignant Neoplasm of the Ureter", "malignant neoplasm of the ureter", "malignant neosplasm of the ureter", "Malignant tumor of ureter (disorder)", "malignant neoplasm of ureter (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ureter cancer", "shortest_name_length": 9}
{"curie": "UMLS:C0861461", "names": ["Colon cancer stage 4", "Stage IV Colon Cancer", "Colon carcinoma Dukes D", "Carcinoma colon Dukes D", "Dukes D Colon Carcinoma", "Stage IV Colon Carcinoma", "Dukes D Colonic Carcinoma", "Dukes D Carcinoma of Colon", "COLON NOS CANCER METASTATIC", "carcinoma of colon, stage IV", "Carcinoma of colon, stage IV", "Stage IV Colon Cancer AJCC v6", "Colon Cancer Stage IV AJCC v6", "AJCC Stage IV Colon Cancer v6", "Colon Cancer, Stage IV AJCC v6", "Dukes D Carcinoma of the Colon", "Astler-Coller D Colon Carcinoma", "Stage IV Colon Carcinoma AJCC v6", "Stage IV Colonic Carcinoma AJCC v6", "Stage IV Carcinoma of Colon AJCC v6", "Carcinoma of colon, stage IV (finding)", "Stage IV Carcinoma of the Colon AJCC v6", "carcinoma of colon, stage IV (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Colon Carcinoma", "shortest_name_length": 20}
{"curie": "MONDO:0013641", "names": ["WARBM2", "micro syndrome 2", "Micro Syndrome 2", "MICRO SYNDROME 2", "Warburg micro syndrome 2", "WARBURG MICRO SYNDROME 2", "WARBURG micro syndrome 2", "Warburg micro syndrome type 2", "RAB3GAP2 Warburg micro syndrome", "Warburg micro syndrome caused by mutation in RAB3GAP2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Warburg micro syndrome 2", "shortest_name_length": 6}
{"curie": "MONDO:0004531", "names": ["sclerosing adenosis", "Breast Sclerosing Adenosis", "Sclerosing Breast Adenosis", "breast sclerosing adenosis", "sclerosing breast adenosis", "Sclerosing breast Adenosis", "sclerosing adenosis of breast", "Sclerosing Adenosis of Breast", "Sclerosing adenosis of breast", "sclerosing adenosis of the breast", "Sclerosing Adenosis of the Breast", "Sclerosing adenosis of breast (disorder)", "sclerosing adenosis of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sclerosing adenosis of breast", "shortest_name_length": 19}
{"curie": "MONDO:0007156", "names": ["Sacroiliitis", "sacroileitis", "sacroiliitis", "SACROILIITIS", "SACROILEITIS", "Sacroiliitides", "Sacroiliitis, NOS", "sacroiliac arthritis", "Sacroiliac arthritis", "arthritis sacroiliac", "Arthritis;sacroiliac", "SACROILIAC ARTHRITIS", "Arthritis, Sacroiliac", "ARTHRITIS, SACROILIAC", "arthritis, sacroiliac", "inflammation sacroiliac", "Sacroiliac joint active", "sacroiliac inflammation", "SACROILIAC INFLAMMATION", "sacroiliitis (diagnosis)", "Sacroiliac joint inflamed", "Sacroiliac joint arthritis", "inflammation joint sacroiliac", "sacroiliac joint inflammation", "inflammation; joint, sacroiliac", "joint; inflammation, sacroiliac", "inflammation of sacroiliac joint", "Inflammation of sacroiliac joint", "Inflammation of sacroiliac joint NOS", "Inflammation of sacroiliac joint, NOS", "Inflammation of sacroiliac joint (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthritis, sacroiliac", "shortest_name_length": 12}
{"curie": "MONDO:0044001", "names": ["Deafness;mixed", "Mixed deafness", "mixed deafness", "HEARING LOSS MIXED", "mixed hearing loss", "Mixed hearing loss", "Mixed Hearing Loss", "hearing loss, mixed", "Mixed type deafness", "Hearing loss, mixed", "loss, mixed hearing", "Hearing Loss, Mixed", "Loss, Mixed Hearing", "mixed type deafness", "Deafness, mixed type", "Losses, mixed hearing", "Losses, Mixed Hearing", "Mixed hearing impairment", "MHL - Mixed hearing loss", "Mixed hearing loss, unspecified", "Mixed Conductive and Sensorineural Deafness", "mixed conductive and sensorineural deafness", "Mixed conductive and sensorineural deafness", "Hearing Loss, Mixed Conductive Sensorineural", "hearing loss, mixed conductive sensorineural", "hearing loss, mixed conductive-sensorineural", "Hearing loss, mixed conductive-sensorineural", "deafness; mixed conductive and sensorineural", "Hearing Loss, Mixed Conductive-Sensorineural", "mixed; deafness (conductive and sensorineural)", "Mixed conductive AND sensorineural hearing loss", "Mixed Conductive and Sensorineural Hearing Loss", "Mixed conductive and sensorineural hearing loss", "mixed conductive and sensorineural hearing loss", "Hearing loss (sensorineural, mixed, and conductive)", "Mixed conductive AND sensorineural hearing loss (disorder)", "mixed conductive and sensorineural hearing loss (diagnosis)", "Mixed conductive and sensorineural hearing loss, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, mixed conductive-sensorineural", "shortest_name_length": 14}
{"curie": "MONDO:0014101", "names": ["MDDGA12", "POMK muscular dystrophy-dystroglycanopathy, type A", "congenital muscular dystrophy-dystroglycanopathy type A12", "Walker-Warburg syndrome or muscle-eye-brain disease POMK-related", "Walker-Warburg syndrome or muscle-eye-brain disease, POMK-related", "WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMK-RELATED", "muscular dystrophy-dystroglycanopathy, type A caused by mutation in POMK", "congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A12", "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12", "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12", "shortest_name_length": 7}
{"curie": "MONDO:0022509", "names": ["asternia", "absent sternum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "asternia", "shortest_name_length": 8}
{"curie": "MONDO:0010619", "names": ["HYP", "XLH", "HPDR", "XLHR", "VDRR", "Vit D resistant rickets", "X-LINKED HYPOPHOSPHATEMIA", "hypophophatemia, X-linked", "X-linked hypophosphatemia", "X-Linked Hypophosphatemia", "x-linked hypophosphatemia", "Familial hypophosphatemia", "HYPOPHOSPHATEMIA, X-LINKED", "hypophosphatemia, X-linked", "Familial hypophosphataemia", "Vitamin D-Resistant Rickets", "Vitamin D-resistant Rickets", "Hereditary hypophosphatemia", "Vitamin D-resistant rickets", "vitamin D-resistant rickets", "VITAMIN D RESISTANT RICKETS", "Rickets, vitamin D resistant", "rickets, vitamin D-resistant", "Hereditary hypophosphataemia", "Rickets, Vitamin D Resistant", "Rickets, Vitamin D-Resistant", "Rickets - vitamin D resistant", "Rickets (vitamin D resistant)", "osteomalacia vitamin D resistant", "Vitamin D-resistant osteomalacia", "vitamin D resistant osteomalacia", "vitamin D-resistant osteomalacia", "X-linked Hypophosphatemic Rickets", "X-linked hypophosphatemic rickets", "Familial hypophosphatemic rickets", "hypophosphatemic rickets, X-linked", "Familial hypophosphataemic rickets", "X-linked hypophosphataemic rickets", "Acquired Vitamin D Resistant Rickets", "Familial vitamin D-resistant rickets", "X-linked vitamin D-resistant rickets", "Acquired Vitamin D-Resistant Rickets", "Vitamin D Resistant Rickets, X Linked", "vitamin D-resistant rickets, X-linked", "Vitamin D-Resistant Rickets, X-Linked", "VITAMIN D-RESISTANT RICKETS, X-LINKED", "X-linked hypophosphatemic osteomalacia", "Familial hypophosphatemic osteomalacia", "Familial hypophosphatemic bone disease", "X-linked hypophosphataemic osteomalacia", "Hereditary 1,25(OH)2D-resistant Rickets", "Familial hypophosphataemic bone disease", "Familial hypophosphataemic osteomalacia", "X-Linked Dominant Hypophosphatemic Rickets", "X-linked Dominant Hypophosphatemic Rickets", "hypophosphatemic rickets X-linked dominant", "X-linked dominant hypophosphatemic rickets", "Hypophosphatemic Rickets, X Linked Dominant", "HYPOPHOSPHATEMIC RICKETS, X-LINKED DOMINANT", "hypophophatemic vitamin D-resistant rickets", "hypophosphatemic rickets, X-linked dominant", "Hypophosphatemic Rickets, X-Linked Dominant", "X-linked hereditary hypophosphatemic rickets", "vitamin D resistant osteomalacia (diagnosis)", "Hypophosphatemic vitamin D-resistant rickets", "Hypophosphatemic Vitamin D Resistant Rickets", "hypophosphatemic vitamin D-resistant rickets", "vitamin D resistant hypophosphatemic rickets", "Hypophosphatemic Vitamin D-resistant Rickets", "HYPOPHOSPHATEMIC VITAMIN D-RESISTANT RICKETS", "Hypophosphatemic Vitamin D-Resistant Rickets", "hypophosphatemia, vitamin D-resistant rickets", "Hypophosphatemia, Vitamin D-Resistant Rickets", "hereditary hypophosphatemic rickets, X-linked", "HPDR I - Hypophosphatemic vitamin D-resistant rickets", "HPDR I - Hypophosphataemic vitamin D-resistant rickets", "vitamin D resistant hypophosphatemic rickets (diagnosis)", "hypophosphatemic rickets, X-linked dominant, X-linked dominant", "Familial x-linked hypophosphatemic vitamin D refractory rickets", "Familial x-linked hypophosphataemic vitamin D refractory rickets", "Familial/hereditary vitamin D-resistant rickets with hypophosphatemia", "Familial x-linked hypophosphatemic vitamin D refractory rickets (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked dominant hypophosphatemic rickets", "shortest_name_length": 3}
{"curie": "UMLS:C0266645", "names": ["Situs inversus thoracis", "Situs Inversus Thoracis", "Transposition of thoracic organs", "Transposition of thoracic viscera", "Transposition of viscera, thoracic", "Situs inversus thoracis (disorder)", "Situs inversus or transversus thoracis", "Situs inversus or transversus, thoracis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Situs inversus thoracis", "shortest_name_length": 23}
{"curie": "UMLS:C5418783", "names": ["Alveolar Ridge Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alveolar Ridge Squamous Cell Carcinoma", "shortest_name_length": 38}
{"curie": "UMLS:C1336236", "names": ["Fallopian Tube Cancer Stage IIIC", "stage IIIC fallopian tube cancer", "Stage IIIC Fallopian Tube Cancer", "fallopian tube cancer stage IIIC", "AJCC stage IIIC fallopian tube cancer", "AJCC Stage IIIC Fallopian Tube Cancer", "FIGO stage IIIC fallopian tube carcinoma", "FIGO Stage IIIC Fallopian Tube Carcinoma", "Stage IIIC Fallopian Tube Cancer AJCC v7", "stage IIIC fallopian tube cancer AJCC v7", "FIGO stage IIIC carcinoma of fallopian tube", "FIGO Stage IIIC Carcinoma of Fallopian Tube", "FIGO stage IIIC carcinoma of the fallopian tube", "FIGO Stage IIIC Carcinoma of the Fallopian Tube"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Fallopian Tube Cancer AJCC v7", "shortest_name_length": 32}
{"curie": "MONDO:0011261", "names": ["SEDN", "Spondyloepiphyseal dysplasia Nishimura type", "SPONDYLOEPIPHYSEAL DYSPLASIA, NISHIMURA TYPE", "spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataract-intellectual disability syndrome", "Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome", "Spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome", "SPONDYLOEPIPHYSEAL DYSPLASIA WITH CORONAL CRANIOSYNOSTOSIS, CATARACTS, CLEFT PALATE, AND MENTAL RETARDATION", "Spondyloepiphyseal Dysplasia With Coronal Craniosynostosis, Cataracts, Cleft Palate, And Mental Retardation", "spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and mental retardation", "spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and intellectual disability", "Spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome (disorder)", "Spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and intellectual disability", "shortest_name_length": 4}
{"curie": "UMLS:C4329667", "names": ["CMML-0", "Chronic Myelomonocytic Leukemia-0"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic Myelomonocytic Leukemia-0", "shortest_name_length": 6}
{"curie": "UMLS:C0862090", "names": ["Grade II LYG", "Grade II Lymphomatoid Granulomatosis", "grade II lymphomatoid granulomatosis", "Angiocentric immunoproliferative lesion grade 2", "Angiocentric Immunoproliferative Lesion Grade II", "Grade II Angiocentric Immunoproliferative Lesion", "Grade II Angiocentric Immunoproliferative Lesions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Angiocentric immunoproliferative lesion grade 2", "shortest_name_length": 12}
{"curie": "MONDO:0018587", "names": ["non-recovering OBPI", "non-recovering OBPL", "chronic obstetric brachial plexus palsy", "chronic obstetric brachial plexus injury", "non-recovering obstetric brachial plexus lesion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-recovering obstetric brachial plexus lesion", "shortest_name_length": 19}
{"curie": "MONDO:0013704", "names": ["MRT30", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 30", "mental retardation, autosomal recessive 30", "intellectual disability, autosomal recessive 30", "autosomal recessive intellectual developmental disorder 30", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 30"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 30", "shortest_name_length": 5}
{"curie": "MONDO:0008457", "names": ["SCA6", "Spinocerebellar Ataxia 6", "SPINOCEREBELLAR ATAXIA 6", "Spinocerebellar Ataxia-6", "spinocerebellar ataxia 6", "Spinocerebellar Ataxia 6s", "Ataxia 6, Spinocerebellar", "Spinocerebellar Ataxia Type 6", "Type 6 Spinocerebellar Ataxia", "spinocerebellar ataxia type 6", "Spinocerebellar ataxia type 6", "Spinocerebellar ataxia type 6 (disorder)", "Spinocerebellar Ataxia Type 6 (disorder)", "CACNA1A autosomal dominant cerebellar ataxia type III", "autosomal dominant cerebellar ataxia type III caused by mutation in CACNA1A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia type 6", "shortest_name_length": 4}
{"curie": "MONDO:0013608", "names": ["JBTS13", "Joubert syndrome 13", "JOUBERT SYNDROME 13", "TCTN1 Joubert syndrome", "Joubert syndrome type 13", "Joubert syndrome caused by mutation in TCTN1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome 13", "shortest_name_length": 6}
{"curie": "MONDO:0010647", "names": ["SPGFX2", "TEX11 azoospermia", "X-linked spermatogenic failure 2", "SPERMATOGENIC FAILURE, X-LINKED, 2", "spermatogenic failure, X-linked, 2", "MALE INFERTILITY FROM DEFECT IN MEIOSIS", "spermatogenic failure, X-linked, type 2", "Male infertility from defect in meiosis", "azoospermia caused by mutation in TEX11", "spermatogenic failure, X-linked, 2, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure, X-linked, 2", "shortest_name_length": 6}
{"curie": "MONDO:0013986", "names": ["COXPD14", "combined oxidative phosphorylation deficiency 14", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14", "combined oxidative phosphorylation defect type 14", "Combined oxidative phosphorylation defect type 14", "FARS2 combined oxidative phosphorylation deficiency", "combined oxidative phosphorylation deficiency type 14", "COXPD14 - combined oxidative phosphorylation defect type 14", "Combined oxidative phosphorylation defect type 14 (disorder)", "combined oxidative phosphorylation deficiency caused by mutation in FARS2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation defect type 14", "shortest_name_length": 7}
{"curie": "UMLS:C0149531", "names": ["Hip Fracture", "PELVIS FRACTURE", "Fracture;pelvis", "Pelvic fracture", "PELVIC FRACTURE", "pelvic fracture", "Pelvic fractures", "pelvis; fracture", "pelvic fractures", "PELVIS, FRACTURE", "fractured pelvis", "fracture; pelvic", "Pelvic fracture(s)", "Fracture of Pelvis", "fracture of pelvis", "Fracture of pelvis", "Fractured pelvis NOS", "Fracture of pelvis NOS", "Fracture of pelvis, NOS", "pelvic fracture (diagnosis)", "Fracture of pelvis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fracture of pelvis", "shortest_name_length": 12}
{"curie": "MONDO:0054740", "names": ["BCDS1", "BCD syndrome", "elschnig syndrome", "blepharocheilodontic syndrome", "blepharocheilodontic syndrome 1", "BLEPHAROCHEILODONTIC SYNDROME 1", "CDH1 blepharo-cheilo-odontic syndrome", "clefting, ectropion, and conical teeth", "ectropion, Inferior, with cleft 51P and/Or palate", "Lagophthalmia with bilateral cleft 51P and palate", "blepharo-cheilo-odontic syndrome caused by mutation in CDH1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blepharocheilodontic syndrome 1", "shortest_name_length": 5}
{"curie": "MONDO:0017755", "names": ["bilirubin metabolism disorder", "disorder of bilirubin metabolism", "hereditary bilirubin metabolism disease", "inborn disorder of bilirubin metabolism", "disorder of bilirubin metabolism and excretion", "inborn disorder of bilirubin metabolism and excretion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of bilirubin metabolism", "shortest_name_length": 29}
{"curie": "UMLS:C0751197", "names": ["Fulminant Hepatic Failure with Cerebral Edema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fulminant Hepatic Failure with Cerebral Edema", "shortest_name_length": 45}
{"curie": "UMLS:C1883404", "names": ["Sertoli cell tumor with lipid storage", "Ovarian Sertoli Cell Tumor with Lipid Storage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Sertoli Cell Tumor with Lipid Storage", "shortest_name_length": 37}
{"curie": "MONDO:0024519", "names": ["HRA", "RHDA1", "Renal aplasia", "RENAL APLASIA", "renal aplasia", "Renal Aplasia", "RENAL AGENESIS", "renal agenesis", "renal dysplasia", "dysplasia renal", "Renal dysplasia", "renal adysplasia", "Renal Adysplasia", "Kidney dysplasia", "RENAL ADYSPLASIA", "dysplasia kidney", "kidney dysplasia", "Renal adysplasia", "Dysplastic kidney", "dysplastic kidney", "dysplasia; kidney", "kidney; dysplasia", "dysplasia kidneys", "Dysplastic kidneys", "dysplastic kidneys", "Dysplasia of kidney", "Renotubular dysgenesis", "hereditary renal aplasia", "HEREDITARY RENAL APLASIA", "Hereditary Renal Aplasia", "Renal dysplasia (disorder)", "Congenital renal dysplasia", "renal dysplasia (diagnosis)", "renal adysplasia (diagnosis)", "renal hypodysplasia/aplasia 1", "RENAL HYPODYSPLASIA/APLASIA 1", "Renal Hypodysplasia-aplasia 1", "Congenital renal dysplasia NOS", "Primitive renal tubule syndrome", "Congenital renal dysplasia, NOS", "Selig Benacerraf Greene syndrome", "renal dysplasia, megalocystis, and sirenomelia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal hypodysplasia/aplasia 1", "shortest_name_length": 3}
{"curie": "UMLS:C5418302", "names": ["Resectable Periampullary Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Periampullary Adenocarcinoma", "shortest_name_length": 39}
{"curie": "UMLS:C1332478", "names": ["Benign Heart Germ Cell Tumor", "Benign Cardiac Germ Cell Tumor", "Benign Heart Germ Cell Neoplasm", "Benign Germ Cell Tumor of Heart", "Benign Cardiac Germ Cell Neoplasm", "Benign Germ Cell Neoplasm of Heart", "Benign Germ Cell Tumor of the Heart", "Benign Germ Cell Neoplasm of the Heart"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Cardiac Germ Cell Tumor", "shortest_name_length": 28}
{"curie": "MONDO:0019338", "names": ["Sarcoid", "sarcoid", "SARCOID", "sarcoids", "Sarcoid NOS", "Sarcoidosis", "SARCOIDOSIS", "sarcoidosis", "Sarcoidoses", "Besnier-Boeck", "Boeck sarcoid", "BOECK SARCOID", "Boeck Disease", "Boeck Sarcoid", "Boeck; sarcoid", "Boecks Disease", "sarcoid; Boeck", "Boecks Sarcoid", "Boeck; disease", "Boeck's Disease", "boeck's disease", "Boeck's disease", "Boeck's Sarcoid", "Sarcoidosis NOS", "Boeck's sarcoid", "boeck's sarcoid", "Sarcoid, Boeck's", "Hutchinson-Boeck", "Sarcoidosis, NOS", "schaumann disease", "Schaumann Disease", "schaumann syndrome", "Boecks sarcoidosis", "Schaumann Syndrome", "SCHAUMANN SYNDROME", "Disease, Schaumann", "Syndrome, Schaumann", "schaumann's disease", "Boeck's sarcoidosis", "syndrome; Schaumann", "Schaumann's disease", "lymphogranulomatosis", "Schaumann's Syndrome", "Besnier Boeck Disease", "Lupus pernio, Besnier", "Besnier; lupus pernio", "Besnier Boeck disease", "Besnier-Boeck Disease", "Darier-Roussy sarcoid", "Darier-Roussy Sarcoid", "Syndrome, Schaumann's", "Schaumann's Syndromes", "Darier-Roussy; sarcoid", "Sarcoidosis (disorder)", "sarcoid; Darier-Roussy", "miliary lupoid of boeck", "lupus pernio of Besnier", "Lupus pernio of Besnier", "sarcoidosis (diagnosis)", "Miliary lupoid of Boeck", "Boeck Sarcoid, any site", "Miliary Lupoid of Boeck", "Sarcoidosis, unspecified", "HUTCHINSON-BOECK SYNDROME", "benign lymphogranulomatosis", "Benign Lymphogranulomatosis", "LYMPHOGRANULOMATOSIS, BENIGN", "lymphogranulomatosis; benign", "benign; lymphogranulomatosis", "lymphogranulomatosis (benign)", "Schaumann; disease or syndrome", "Besnier-Boeck-Schaumann disease", "BESNIER-BOECK-SCHAUMANN DISEASE", "Besnier-Boeck-Schaumann Syndrome", "Besnier Boeck Schaumann Syndrome", "Besnier-Boeck-Schaumann syndrome", "besnier-Boeck-Schaumann syndrome", "Besnier-Boeck-Schaumann's disease", "Syndrome, Besnier-Boeck-Schaumann", "Schaumann; benign lymphogranulomatosis", "benign lymphogranulomatosis (diagnosis)", "Benign Lymphogranulomatosis, Schaumann's", "Benign lymphogranulomatosis of Schaumann", "benign lymphogranulomatosis of Schaumann"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sarcoidosis", "shortest_name_length": 7}
{"curie": "MONDO:0011107", "names": ["Hjmd", "HJMD", "Hypotrichosis With Cone-Rod Dystrophy", "hypotrichosis with cone-rod dystrophy", "HYPOTRICHOSIS WITH CONE-ROD DYSTROPHY", "hypotrichosis with juvenile macular dystrophy", "Hypotrichosis with juvenile macular dystrophy", "Juvenile macular degeneration and hypotrichosis", "juvenile macular degeneration and hypotrichosis", "Hypotrichosis with juvenile macular degeneration", "hypotrichosis with juvenile macular degeneration", "Juvenile macular dystrophy and congenital hypotrichosis", "juvenile macular dystrophy and congenital hypotrichosis", "congenital hypotrichosis with juvenile macular dystrophy", "HYPOTRICHOSIS, CONGENITAL, WITH JUVENILE MACULAR DYSTROPHY", "Hypotrichosis, congenital, with juvenile macular dystrophy", "hypotrichosis, congenital, with juvenile macular dystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital hypotrichosis with juvenile macular dystrophy", "shortest_name_length": 4}
{"curie": "MONDO:0016354", "names": ["XP-CS", "XP/CS", "XP/CS complex", "Xeroderma Pigmentosum/Cockayne Syndrome", "Xeroderma Pigmentosum-Cockayne Syndrome Complex", "xeroderma pigmentosum-Cockayne syndrome complex", "Xeroderma pigmentosum-Cockayne syndrome complex", "Xeroderma pigmentosum and Cockayne syndrome complex", "Xeroderma pigmentosum and Cockayne syndrome complex (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "xeroderma pigmentosum-Cockayne syndrome complex", "shortest_name_length": 5}
{"curie": "UMLS:C4553749", "names": ["Stage IV Fallopian Tube Cancer", "Stage IV Fallopian Tube Cancer AJCC v8", "Stage IV Fallopian Tube Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Fallopian Tube Cancer AJCC v8", "shortest_name_length": 30}
{"curie": "MONDO:0010147", "names": ["TONGUE, PIGMENTED FUNGIFORM PAPILLAE OF", "tongue, pigmented fungiform papillae of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tongue, pigmented fungiform papillae of", "shortest_name_length": 39}
{"curie": "MONDO:0007768", "names": ["HPTJT", "HRPT2", "Hpt-Jt", "HPT-JT", "hyperparathyroidism-2", "Hyperparathyroidism-2", "Hyperparathyroidism 2", "hyperparathyroidism 2", "hyperparathyroidism type 2", "familial hyperparathyroidism HRPT2", "familial hyperparathyroidism - hrpt2", "hyperparathyroidism 2 with jaw tumors", "HYPERPARATHYROIDISM 2 WITH JAW TUMORS", "HYPERPARATHYROIDISM-JAW TUMOR SYNDROME", "Hyperparathyroidism Jaw Tumor Syndrome", "hyperparathyroidism-jaw tumor syndrome", "Hyperparathyroidism-jaw tumor syndrome", "Hyperparathyroidism-Jaw Tumor Syndrome", "Hyperparathyroidism-jaw tumour syndrome", "parathyroid adenoma with cystic changes", "Familial cystic parathyroid adenomatosis", "Familial Cystic Parathyroid Adenomatosis", "parathyroid adenomatosis, familial cystic", "PARATHYROID ADENOMATOSIS, FAMILIAL CYSTIC", "Parathyroid Adenomatosis, Familial Cystic", "familial hyperparathyroidism HRPT2 (diagnosis)", "Hereditary Hyperparathyroidism-Jaw Tumor Syndrome", "hereditary hyperparathyroidism-jaw tumor syndrome", "Hyperparathyroidism-jaw tumor syndrome (disorder)", "HYPERPARATHYROIDISM-JAW TUMOR SYNDROME, HEREDITARY", "Hyperparathyroidism-Jaw Tumor Syndrome, Hereditary", "hyperparathyroidism-jaw tumor syndrome, hereditary", "Familial Primary Hyperparathyroidism with Multiple Ossifying Jaw Fibromas", "Familial primary hyperparathyroidism with multiple ossifying jaw fibromas", "familial primary hyperparathyroidism with multiple ossifying jaw fibromas", "hyperparathyroidism, familial primary, with multiple ossifying jaw fibromas", "HYPERPARATHYROIDISM, FAMILIAL PRIMARY, WITH MULTIPLE OSSIFYING JAW FIBROMAS", "Hyperparathyroidism, Familial Primary, with Multiple Ossifying Jaw Fibromas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperparathyroidism 2 with jaw tumors", "shortest_name_length": 5}
{"curie": "UMLS:C5236962", "names": ["Unresectable Nasopharyngeal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Nasopharyngeal Carcinoma", "shortest_name_length": 37}
{"curie": "UMLS:C4331475", "names": ["Unresectable Leiomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Leiomyosarcoma", "shortest_name_length": 27}
{"curie": "UMLS:C1709250", "names": ["Non-Neoplastic Hepatic Disease", "Non-Neoplastic Hepatic Disorder", "Non-Neoplastic Liver and Intrahepatic Bile Duct Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Liver and Intrahepatic Bile Duct Disorder", "shortest_name_length": 30}
{"curie": "MONDO:0005857", "names": ["Morbillivirus Infection", "Infection, Morbillivirus", "Morbillivirus Infections", "Infections, Morbillivirus", "Disease due to Morbillivirus", "DISEASES DUE TO MORBILLIVIRUS", "Disease caused by Morbillivirus", "morbillivirus infectious disease", "Morbillivirus infectious disease", "Morbillivirus disease or disorder", "Disease due to Morbillivirus, NOS", "Morbillivirus caused disease or disorder", "Disease caused by Morbillivirus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "morbillivirus infectious disease", "shortest_name_length": 23}
{"curie": "MONDO:0000417", "names": ["early onset absence epilepsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early onset absence epilepsy", "shortest_name_length": 28}
{"curie": "MONDO:0009354", "names": ["HMAE", "Methylcobalamin deficiency type cblE", "methylcobalamin deficiency type cblE", "METHYLCOBALAMIN DEFICIENCY, cblE TYPE", "Methylcobalamin Deficiency, cblE Type", "Methylcobalamin Deficiency, CblE Type", "methylcobalamin deficiency, cblE type", "homocystinuria-megaloblastic anemia cblE type", "homocystinuria-megaloblastic anemia, cbl e type", "Vitamin B12-Responsive Homocystinuria, CblE Type", "VITAMIN B12-RESPONSIVE HOMOCYSTINURIA, cblE TYPE", "vitamin B12-responsive homocystinuria, cblE type", "homocystinuria due to defect in methylation Cbl e", "Functional methionine synthase deficiency type cblE", "methylmalonic aciduria and homocystinuria type cblE", "functional methionine synthase deficiency type cblE", "HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, cblE COMPLEMENTATION TYPE", "Homocystinuria-Megaloblastic Anemia, cblE Complementation Type", "homocystinuria-megaloblastic anemia, cblE complementation type", "homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism cblE complementation type", "homocystinuria-megaloblastic Anemia due to defect in cobalamin metabolism, cblE complementation type", "Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type", "HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA DUE TO DEFECT IN COBALAMIN METABOLISM, cblE COMPLEMENTATION TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "methylcobalamin deficiency type cblE", "shortest_name_length": 4}
{"curie": "MONDO:0008839", "names": ["AMC Syndrome", "AMC SYNDROME", "AMC syndrome", "ataxia-microcephaly-cataract syndrome", "ATAXIA-MICROCEPHALY-CATARACT SYNDROME", "Ataxia-Microcephaly-Cataract Syndrome", "ataxia-microcephaly-cataract (AMC) syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ataxia-microcephaly-cataract syndrome", "shortest_name_length": 12}
{"curie": "UMLS:C3273101", "names": ["Gallbladder Mucinous Cystic Neoplasm, High Grade", "Gallbladder Mucinous Cystic Neoplasm, High-Grade", "Gallbladder MCN with High Grade Intraepithelial Neoplasia", "Gallbladder Mucinous Cystic Neoplasm with High Grade Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gallbladder Mucinous Cystic Neoplasm, High Grade", "shortest_name_length": 48}
{"curie": "UMLS:C0860361", "names": ["Bone Shedding Debris", "Bone shedding debris", "Debris, bone shedding"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone shedding debris", "shortest_name_length": 20}
{"curie": "MONDO:0006430", "names": ["splenic mantle cell lymphoma", "Splenic Mantle Cell Lymphoma", "Mantle cell lymphoma, spleen", "mantle cell lymphoma of spleen", "Mantle cell lymphoma of spleen", "Mantle cell lymphoma involving spleen", "Mantle cell lymphoma of spleen (disorder)", "mantle cell lymphoma of spleen (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "splenic mantle cell lymphoma", "shortest_name_length": 28}
{"curie": "UMLS:C0742186", "names": ["Cervical root lesion", "Lesion;cervical root", "cervical root lesion", "cervical root lesions", "CERVICAL RADICULOPATHY", "Cervical Radiculopathy", "radiculopathy cervical", "cervical radiculopathy", "Cervical radiculopathy", "lesion of cervical root", "Radiculopathy, Cervical", "Cervical root neuropathy", "Cervical Radiculopathies", "Cervical root lesion, NOS", "Radiculopathies, Cervical", "neuropathy; radicular, cervical", "Cervical radiculopathy (disorder)", "cervical root lesions (diagnosis)", "cervical radiculopathy (diagnosis)", "nerve root and plexus disorder cervical root lesions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radiculopathy, Cervical", "shortest_name_length": 20}
{"curie": "MONDO:0013668", "names": ["tetrasomy 18p", "TETRASOMY 18p", "18p Tetrasomy", "18p tetrasomy", "Tetrasomy 18p", "18p isochromosome", "Isochromosome 18p", "18p Isochromosome", "tetrasomy type 18p", "tetrasomy type 18P", "partial tetrasomy 18p", "Tetrasomy 18p (disorder)", "tetrasomy chromosome 18p", "chromosome 18p tetrasomy", "ISOCHROMOSOME 18p SYNDROME", "Isochromosome 18P syndrome", "Chromosome 18, tetrasomy 18p", "chromosome 18p tetrasomy syndrome", "Tetrasomy, Short Arm of Chromosome 18"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tetrasomy 18p", "shortest_name_length": 13}
{"curie": "UMLS:C0022415", "names": ["TB of the jointe", "joint tuberculosis", "Joint tuberculosis", "Joint Tuberculosis", "Joint Tuberculoses", "Tuberculosis, Joint", "Tuberculoses, Joint", "joints tuberculosis", "Joints--Tuberculosis", "tuberculous arthritis", "of joint tuberculosis", "Tuberculosis of joint", "Tuberculous arthritis", "Tuberculosis;joint(s)", "tuberculosis of joint", "Tuberculous Arthritis", "ARTHRITIS, TUBERCULOUS", "Tuberculous rheumatism", "Tuberculous arthropathy", "tuberculosis of a joint", "Tuberculosis of joint, NOS", "Tuberculous arthritis (disorder)", "tuberculosis of joint (diagnosis)", "Arthritis caused by Mycobacterium tuberculosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joint Tuberculosis", "shortest_name_length": 16}
{"curie": "UMLS:C2861596", "names": ["AML M4 Eo with inv(16) or t(16;16)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AML M4 Eo with inv(16) or t(16;16)", "shortest_name_length": 34}
{"curie": "MONDO:0017815", "names": ["Porencephaly", "Porencephaly, NOS", "Porencephalic cyst", "Acquired porencephaly", "acquired porencephaly", "porencephaly; acquired", "Porencephaly, acquired", "acquired; porencephaly", "Acquired porencephaly (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired porencephaly", "shortest_name_length": 12}
{"curie": "MONDO:0010350", "names": ["POF2A", "Premature Ovarian Failure 2a", "PREMATURE OVARIAN FAILURE 2A", "premature ovarian failure 2A", "DIAPH2 primary ovarian failure", "primary ovarian insufficiency 2A", "premature ovarian failure type 2A", "premature ovarian failure 2A, X-linked dominant", "primary ovarian failure caused by mutation in DIAPH2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "premature ovarian failure 2A", "shortest_name_length": 5}
{"curie": "MONDO:0041825", "names": ["Gram negative meningitis", "Gram negative bacterial meningitis", "gram-negative bacterial meningitis", "Gram-negative bacterial meningitis", "bacterial; meningitis, gram-negative", "meningitis; bacterial, gram-negative", "Meningitis with gram negative bacteria", "meningitis with gram negative bacteria", "Meningitis gram-negative bacterial NOS", "Gram negative bacterial meningitis (diagnosis)", "bacterial meningitis due to gram-negative bacteria", "Bacterial meningitis due to Gram-negative bacteria", "Bacterial meningitis caused by Gram-negative bacteria", "bacterial meningitis caused by gram-negative bacteria", "Bacterial meningitis caused by Gram-negative bacteria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bacterial meningitis caused by gram-negative bacteria", "shortest_name_length": 24}
{"curie": "MONDO:0018645", "names": ["IgG4-related sclerosing cholangitis", "Immunoglobulin G4-related sclerosing cholangitis", "Immunoglobulin G4-related sclerosing cholangitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IgG4-related sclerosing cholangitis", "shortest_name_length": 35}
{"curie": "MONDO:0007442", "names": ["DGI-III", "dentinogenesis imperfecta type 3", "Dentinogenesis imperfecta type 3", "dentinogenesis imperfecta type III", "dentinogenesis imperfecta Shields type 3", "dentinogenesis imperfecta, Shields type 3", "brandywine type dentinogenesis imperfecta", "Brandywine type dentinogenesis imperfecta", "Dentinogenesis imperfecta, shields type 3", "Dentinogenesis imperfecta, Shields type 3", "BRANDYWINE TYPE DENTINOGENESIS IMPERFECTA", "DENTINOGENESIS IMPERFECTA, SHIELDS TYPE III", "dentinogenesis imperfecta, Shields type III", "Dentinogenesis Imperfecta, Shields Type III", "Brandywine type of dentinogenesis imperfecta", "Dentinogenesis imperfecta - Shield's type III", "Dentinogenesis imperfecta - Shield's type III (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dentinogenesis imperfecta type 3", "shortest_name_length": 7}
{"curie": "UMLS:C3829186", "names": ["Stage IIb", "Masaoka Stage IIb", "Masaoka-Koga Stage IIb"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Masaoka-Koga Stage IIb", "shortest_name_length": 9}
{"curie": "MONDO:0019526", "names": ["Bury", "Erythema diutinum", "Erythema elevatum diutinum", "erythema elevatum diutinum", "elevatum diutinum; erythema", "erythema; elevatum diutinum", "EED - Erythema elevatum diutinum", "Erythema elevatum diutinum (disorder)", "erythema elevatum diutinum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythema elevatum diutinum", "shortest_name_length": 4}
{"curie": "MONDO:0012724", "names": ["FCAS2", "NAPS12", "FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 2", "Familial Cold Autoinflammatory Syndrome 2", "familial cold autoinflammatory syndrome 2", "Familial cold autoinflammatory syndrome type 2", "NLRP12 familial cold autoinflammatory syndrome", "familial cold autoinflammatory syndrome type 2", "NLRP12-Associated Hereditary Periodic Fever Syndrome", "NALP12-associated hereditary periodic fever syndrome", "NALP12-Associated Hereditary Periodic Fever Syndrome", "NLRP12-associated hereditary periodic fever syndrome", "FCAS2 - familial cold autoinflammatory syndrome type 2", "familial cold autoinflammatory syndrome caused by mutation in NLRP12", "NLR family pyrin domain containing 12-associated hereditary periodic fever syndrome", "NLR family pyrin domain containing 12-associated hereditary periodic fever syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial cold autoinflammatory syndrome 2", "shortest_name_length": 5}
{"curie": "UMLS:C4726546", "names": ["Recurrent Metastatic Digestive System Carcinoma", "Recurrent Metastatic Gastrointestinal System Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Metastatic Digestive System Carcinoma", "shortest_name_length": 47}
{"curie": "UMLS:C3273136", "names": ["Intrahepatic Bile Duct IPN with an Associated Invasive Carcinoma", "Intrahepatic Bile Duct Papillary Neoplasm with an Associated Invasive Carcinoma", "Intrahepatic Bile Duct Intraductal Papillary Neoplasm with an Associated Invasive Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intrahepatic Bile Duct Intraductal Papillary Neoplasm with an Associated Invasive Carcinoma", "shortest_name_length": 64}
{"curie": "MONDO:0011181", "names": ["CFEOM2", "FEOM2 LOCUS", "Feom2 locus", "Fibrosis Of Extraocular Muscles, Congenital, 2", "FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 2", "fibrosis of extraocular muscles, congenital, 2", "congenital fibrosis of the extraocular muscles 2", "PHOX2A congenital fibrosis of extraocular muscles", "fibrosis of extraocular muscles, congenital, type 2", "FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, AUTOSOMAL RECESSIVE", "fibrosis of extraocular muscles, congenital, autosomal recessive", "Fibrosis Of Extraocular Muscles, Congenital, Autosomal Recessive", "congenital fibrosis of extraocular muscles caused by mutation in PHOX2A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibrosis of extraocular muscles, congenital, 2", "shortest_name_length": 6}
{"curie": "UMLS:C0282643", "names": ["Smith Lemli Opitz Syndrome, Type I", "Smith Lemli Opitz syndrome, type 1", "Smith-Lemli-Opitz Syndrome, Type 1", "Smith-Lemli-Opitz Syndrome, Type I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Smith-Lemli-Opitz Syndrome, Type I", "shortest_name_length": 34}
{"curie": "MONDO:0001021", "names": ["Ametropic amblyopia", "ametropic amblyopia", "Meridional amblyopia", "Refractive amblyopia", "meridional amblyopia", "refractive amblyopia", "Amblyopia, refractive", "Refractive amblyopia (disorder)", "refractive amblyopia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ametropic amblyopia", "shortest_name_length": 19}
{"curie": "MONDO:0008892", "names": ["PFIC1", "BYLER DISEASE", "Byler disease", "Byler syndrome", "FIC1 deficiency", "Byler's disease", "severe ATP8B1 deficiency", "cholestasis, fatal intrahepatic", "Cholestasis, fatal intrahepatic", "Progressive familial intrahepatic cholestasis", "progressive familial intrahepatic cholestasis", "progressive familial intrahepatic cholestasis 1", "Cholestasis, progressive familial intrahepatic 1", "cholestasis, progressive familial intrahepatic 1", "CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 1", "cholestasis, progressive familial intrahepatic, 1", "Cholestasis, Progressive Familial Intrahepatic, 1", "Progressive familial intrahepatic cholestasis type 1", "progressive familial intrahepatic cholestasis type 1", "cholestasis, progressive familial intrahepatic, type 1", "PFIC1 Progressive familial intrahepatic cholestasis type 1", "Progressive familial intrahepatic cholestasis type 1 (PFIC1)", "PFIC1 - progressive familial intrahepatic cholestasis type 1", "Progressive familial intrahepatic cholestasis type 1 (PFIC 1)", "Progressive familial intrahepatic cholestasis type 1 (disorder)", "progressive familial intrahepatic cholestasis type 1 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive familial intrahepatic cholestasis type 1", "shortest_name_length": 5}
{"curie": "UMLS:C1275323", "names": ["Skin Plasmacytoma", "Plasmacytoma of Skin", "Cutaneous Plasmacytoma", "Primary Cutaneous Plasmacytoma", "Primary cutaneous plasmacytoma", "Primary Extraosseous Skin Plasmacytoma", "Primary Extramedullary Skin Plasmacytoma", "Primary cutaneous plasmacytoma (disorder)", "Primary Extraosseous Plasmacytoma of Skin", "Primary cutaneous plasmacytoma (diagnosis)", "Primary Extraosseous Cutaneous Plasmacytoma", "Primary Extramedullary Plasmacytoma of Skin", "Primary cutaneous plasmacytic B-cell lymphoma", "Primary Extramedullary Cutaneous Plasmacytoma", "Primary cutaneous plasmacytoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary cutaneous plasmacytoma", "shortest_name_length": 17}
{"curie": "MONDO:0014326", "names": ["NEM9", "nemaline myopathy 9", "NEMALINE MYOPATHY 9", "KLHL41 nemaline myopathy", "nemaline myopathy type 9", "nemaline myopathy caused by mutation in KLHL41"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nemaline myopathy 9", "shortest_name_length": 4}
{"curie": "MONDO:0013066", "names": ["SRXY3", "46XY sex reversal 3", "46,XY Sex Reversal 3", "46,XY SEX reversal 3", "46,XY sex reversal 3", "46,XY SEX REVERSAL 3", "46,XY Sex reversal type 3", "sex reversal, XY, with or without adrenal failure", "Sex Reversal, XY, With Or Without Adrenal Failure", "DISORDER OF SEX DEVELOPMENT, 46,XY, NR5A1-RELATED", "disorder of sex development, 46,XY, NR5A1-related", "SEX REVERSAL, XY, WITH OR WITHOUT ADRENAL FAILURE", "disorder of Sex development, 46,XY, Nr5A1-related", "Sex reversal, XY, with or without adrenal failure", "46,XY sex reversal, partial or complete, NR5A1-related", "46,XY SEX REVERSAL, PARTIAL OR COMPLETE, NR5A1-RELATED", "46,XY Sex reversal, partial or complete, Nr5A1-related", "46,XY Sex Reversal, Partial or Complete, NR5A1-Related", "46,XY GONADAL DYSGENESIS, PARTIAL OR COMPLETE, WITH OR WITHOUT ADRENAL FAILURE", "46,XY Gonadal Dysgenesis, Complete or Partial, With or Without Adrenal Failure", "46,XY gonadal dysgenesis, partial or complete, with or without adrenal failure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XY sex reversal 3", "shortest_name_length": 5}
{"curie": "MONDO:0012623", "names": ["MRT4", "mental retardation, autosomal recessive 4", "Mental Retardation, Autosomal Recessive 4", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 4", "mental retardation, autosomal recessive, 4", "intellectual disability, autosomal recessive 4", "autosomal recessive intellectual developmental disorder 4", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 4", "shortest_name_length": 4}
{"curie": "MONDO:0005773", "names": ["GS", "Gerstmann", "Gerstmann tetrad", "GERSTMANN SYNDROME", "gerstmann syndrome", "Gerstmann syndrome", "Gerstmann Syndrome", "gerstmanns syndrome", "Syndrome, Gerstmann", "Gerstmann's Syndrome", "Gerstmann's syndrome", "gerstmann's syndrome", "Syndrome de Gerstmann", "ANGULAR GYRUS SYNDROME", "de Gerstmann, Syndrome", "Gerstmann, Syndrome de", "Gerstmann-Badal Syndrome", "Gerstmann Badal Syndrome", "Gerstmann Badal syndrome", "Syndrome, Gerstmann-Badal", "Aphasia-angular gyrus syndrome", "aphasia-angular gyrus syndrome", "developmental Gerstmann syndrome", "Aphasia-angular gyrus syndrome (disorder)", "Finger-Agnosia-Left-Right-Confusion-Acalculia-Agraphia", "Finger-Agnosia-Left-Right-Confusion-Acalculia-Agraphias"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gerstmann syndrome", "shortest_name_length": 2}
{"curie": "UMLS:C4683645", "names": ["Childhood Non-Hodgkin Lymphoma by Ann Arbor Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Non-Hodgkin Lymphoma by Ann Arbor Stage", "shortest_name_length": 49}
{"curie": "MONDO:0007405", "names": ["Cfd1", "CFD1", "Crouzon", "Crouzon Disease", "crouzon disease", "Crouzon disease", "Crouzon syndrome", "crouzons disease", "CROUZON SYNDROME", "Crouzon Syndrome", "crouzon syndrome", "Crouzons Disease", "crouzons syndrome", "Crouzon's Disease", "Crouzon's disease", "crouzon's disease", "Crouzon's syndrome", "crouzon's syndrome", "syndrome crouzon's", "Apert-Crouzon syndrome", "Vogt cephalosyndactyly", "Craniofacial dysostosis", "Craniofacial Dysostoses", "craniofacial dysostosis", "Craniofacial Dysostosis", "dysostosis; craniofacial", "Dysostoses, Craniofacial", "craniofacial; dysostosis", "Dysostosis, Craniofacial", "Craniofacial Dysarthroses", "Craniofacial Dysarthrosis", "craniofacial dysarthrosis", "Dysarthrosis, Craniofacial", "Dysarthroses, Craniofacial", "Crouzon syndrome (disorder)", "Crouzon's disease (diagnosis)", "Acrocephalosyndactyly, type II", "Craniofacial dysostosis type 1", "craniofacial dysostosis type 1", "Craniofacial Dysostosis Type 1", "Crouzon Craniofacial Dysostosis", "Crouzon craniofacial dysostosis", "CROUZON CRANIOFACIAL DYSOSTOSIS", "CRANIOFACIAL DYSOSTOSIS, TYPE I", "craniofacial dysostosis, type 1", "Craniofacial Dysostosis, Type I", "Craniofacial Dysostosis Syndrome", "Craniofacial dysostosis syndrome", "syndrome craniofacial dysostosis", "Craniofacial Dysostosis, Crouzon", "Craniofacial Dysostosis Syndromes", "congenital deformity of head Crouzon's disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Crouzon syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C4682804", "names": ["Stage IIA Testicular Cancer", "Stage IIA Testicular Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Testicular Cancer AJCC v8", "shortest_name_length": 27}
{"curie": "MONDO:0700091", "names": ["r", "Ring chromosome", "chromosome ring", "Ring Chromosome", "ring chromosome", "Chromosome, Ring", "Ring Chromosomes", "ring chromosomes", "Chromosomes, Ring", "ring chromosome disorder", "Ring chromosome (disorder)", "Supernumerary Circular Chromosome", "supernumerary circular chromosome", "Ring chromosome (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ring chromosome disorder", "shortest_name_length": 1}
{"curie": "MONDO:0009045", "names": ["CROME SYNDROME", "crome syndrome", "Crome syndrome", "cataract-nephropathy-encephalopathy syndrome", "Cataract-nephropathy-encephalopathy syndrome", "Congenital cataract, nephropathy, encephalopathy syndrome", "congenital cataract, nephropathy, encephalopathy syndrome", "Congenital cataract, nephropathy, encephalopathy syndrome (disorder)", "congenital cataract, nephropathy, encephalopathy syndrome (diagnosis)", "congenital cataracts, renal tubular necrosis and encephalopathy in two sisters"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract-nephropathy-encephalopathy syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0002623", "names": ["osteosarcoma", "Osteosarcoma", "childhood osteosarcoma", "pediatric osteosarcoma", "Childhood Osteosarcoma", "Pediatric Osteosarcoma", "Osteosarcoma in children", "Childhood Osteogenic Sarcoma", "childhood osteogenic sarcoma", "childhood osteosarcoma (disease)", "pediatric osteosarcoma (disease)", "osteosarcoma (disease) of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pediatric osteosarcoma", "shortest_name_length": 12}
{"curie": "MONDO:0041259", "names": ["diphtheritic myocarditis", "Diphtheritic myocarditis", "diphtheritis myocarditis", "myocarditis; diphtheria (etiology)", "diphtheria; myocarditis (etiology)", "Diphtheritic myocarditis (disorder)", "diphtheritic myocarditis (diagnosis)", "diphtheria; myocarditis (manifestation)", "Corynebacterium diphtheriae myocarditis", "myocarditis; diphtheria (manifestation)", "Corynebacterium diphtheriae caused myocarditis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diphtheritic myocarditis", "shortest_name_length": 24}
{"curie": "UMLS:C4525043", "names": ["Stage IV Appendix Cancer", "Stage IV Appendix Carcinoma AJCC v8", "Stage IV Appendiceal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Appendix Carcinoma AJCC v8", "shortest_name_length": 24}
{"curie": "MONDO:0010903", "names": ["CRSA", "craniosynostosis, Adelaide type", "Craniosynostosis, Adelaide Type", "CRANIOSYNOSTOSIS, ADELAIDE TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniosynostosis, Adelaide type", "shortest_name_length": 4}
{"curie": "UMLS:C3670617", "names": ["Immune-mediated dermatitis", "Immune mediated dermatitis", "Immune mediated dermatitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immune mediated dermatitis", "shortest_name_length": 26}
{"curie": "MONDO:0012737", "names": ["lqt10", "LQT10", "ATFB17", "lqt10 (diagnosis)", "LONG QT SYNDROME 10", "long QT syndrome 10", "Long Qt Syndrome 10", "SCN4B long QT syndrome", "long QT syndrome type 10", "atrial fibrillation, familial, 17", "ATRIAL FIBRILLATION, FAMILIAL, 17", "long QT syndrome caused by mutation in SCN4B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "long QT syndrome 10", "shortest_name_length": 5}
{"curie": "UMLS:C1412002", "names": ["pneumonia walk", "walking pneumonia", "Walking pneumonia", "pneumonia walking", "Walking Pneumonia", "PNEUMONIA ATYPICAL", "Atypical Pneumonia", "atypical pneumonia", "Atypical pneumonia", "Pneumonia;atypical", "atypical; pneumonia", "PNEUMONIA, ATYPICAL", "pneumonia; atypical", "Atypical pneumonia (disorder)", "atypical pneumonia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypical pneumonia", "shortest_name_length": 14}
{"curie": "MONDO:0009516", "names": ["absence deformity of leg-cataract syndrome", "LEG, ABSENCE DEFORMITY OF, WITH CONGENITAL CATARACT", "leg, absence deformity of, with congenital cataract", "Leg, Absence Deformity of, with Congenital Cataract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "absence deformity of leg-cataract syndrome", "shortest_name_length": 42}
{"curie": "MONDO:0003495", "names": ["ovarian squamous cell tumor", "Ovarian Squamous Cell Tumor", "ovary squamous cell neoplasm", "ovarian squamous cell neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian squamous cell neoplasm", "shortest_name_length": 27}
{"curie": "UMLS:C2981665", "names": ["Stage IB Distal Bile Duct Cancer", "Stage IB Distal Bile Duct Cancer AJCC v7", "Stage IB Extrahepatic (Distal) Bile Duct Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Distal Bile Duct Cancer AJCC v7", "shortest_name_length": 32}
{"curie": "MONDO:0016142", "names": ["Beta sarcoglycanopathy", "Beta-sarcoglycanopathy", "beta-sarcoglycanopathy", "qualitative or quantitative defects of beta-sarcoglycan"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of beta-sarcoglycan", "shortest_name_length": 22}
{"curie": "UMLS:C1707876", "names": ["Early Unfavorable Non-Hodgkin Lymphoma", "Early Unfavorable Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Early Unfavorable Non-Hodgkin Lymphoma", "shortest_name_length": 38}
{"curie": "MONDO:0011814", "names": ["SMC", "SMC1", "Smc1", "Smith-McCort dysplasia", "SMITH-McCort dysplasia 1", "Smith-McCort dysplasia 1", "SMITH-McCORT DYSPLASIA 1", "SMITH-MCCORT DYSPLASIA 1", "DYM Smith-McCort dysplasia", "Smith-McCort dysplasia type 1", "Smith-McCort dysplasia caused by mutation in DYM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Smith-McCort dysplasia 1", "shortest_name_length": 3}
{"curie": "MONDO:0011309", "names": ["Familial gestational hyperthyroidism", "familial gestational hyperthyroidism", "hyperthyroidism, familial gestational", "Hyperthyroidism, Familial Gestational", "HYPERTHYROIDISM, FAMILIAL GESTATIONAL", "Familial gestational hyperthyroidism (disorder)", "familial gestational hyperthyroidism (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial gestational hyperthyroidism", "shortest_name_length": 36}
{"curie": "MONDO:0033554", "names": ["IMD73B", "IMMUNODEFICIENCY 73B WITH DEFECTIVE NEUTROPHIL CHEMOTAXIS AND LYMPHOPENIA", "immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia", "shortest_name_length": 6}
{"curie": "UMLS:C3665893", "names": ["Herpes zoster cutaneous disseminated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Herpes zoster cutaneous disseminated", "shortest_name_length": 36}
{"curie": "MONDO:0001654", "names": ["Spermatic cord Ca", "spermatic cord Ca", "spermatic cord cancer", "cancer of spermatic cord", "Malignant Spermatic Cord Tumor", "malignant spermatic cord tumor", "SPERMATIC CORD, MALIGNANT TUMOR", "Malignant Tumor of Spermatic Cord", "malignant tumor of spermatic cord", "Malignant tumor of spermatic cord", "malignant spermatic cord neoplasm", "Malignant Spermatic Cord Neoplasm", "Malignant tumour of spermatic cord", "Malignant Neoplasm of Spermatic Cord", "Malignant neoplasm of spermatic cord", "malignant neoplasm of spermatic cord", "malignant tumor of the Spermatic Cord", "malignant tumor of the spermatic cord", "Malignant Tumor of the Spermatic Cord", "Malignant Neoplasm of the Spermatic Cord", "malignant neoplasm of the spermatic cord", "Malignant tumor of spermatic cord (disorder)", "malignant neoplasm of spermatic cord (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatic cord cancer", "shortest_name_length": 17}
{"curie": "MONDO:0021083", "names": ["FEOM1", "CFEOM1", "CFEOM3B", "Feom1 locus", "FEOM1 LOCUS", "ophthalmoplegia, congenital", "Ophthalmoplegia, Congenital", "OPHTHALMOPLEGIA, CONGENITAL", "blepharoptosis with absent eye movements", "BLEPHAROPTOSIS WITH ABSENT EYE MOVEMENTS", "Blepharoptosis with Absent Eye Movements", "Fibrosis Of Extraocular Muscles, Congenital, 1", "FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 1", "fibrosis of extraocular muscles, congenital, 1", "FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3B", "Fibrosis of Extraocular Muscles, Congenital, 3B", "fibrosis of extraocular muscles, congenital, 3B", "congenital fibrosis of the extraocular muscles 1", "KIF21A congenital fibrosis of extraocular muscles", "congenital fibrosis of extraocular muscles type 1", "congenital fibrosis of extraocular muscles caused by mutation in KIF21A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital fibrosis of extraocular muscles type 1", "shortest_name_length": 5}
{"curie": "MONDO:0009103", "names": ["DIH2", "diaphragmatic hernia 2", "Diaphragmatic Hernia 2", "DIAPHRAGMATIC HERNIA 2", "hernia, congenital diaphragmatic 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diaphragmatic hernia 2", "shortest_name_length": 4}
{"curie": "MONDO:0012406", "names": ["HRPT3", "hyperparathyroidism 3", "Hyperparathyroidism 3", "HYPERPARATHYROIDISM 3", "hyperparathyroidism, familial isolated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperparathyroidism 3", "shortest_name_length": 5}
{"curie": "MONDO:0004500", "names": ["Superior Sulcus Lung Carcinoma", "lung superior sulcus carcinoma", "superior sulcus lung carcinoma", "Superior Sulcus Carcinoma of Lung", "superior sulcus carcinoma of lung", "Superior Sulcus Carcinoma of the Lung", "superior sulcus carcinoma of the lung", "Superior Sulcus carcinoma of the lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung superior sulcus carcinoma", "shortest_name_length": 30}
{"curie": "UMLS:C1334420", "names": ["Low Grade Cervical Glandular Intraepithelial Neoplasia", "Low grade cervical glandular intraepithelial neoplasia", "L-CGIN - low grade cervical glandular intraepithelial neoplasia", "Low grade cervical glandular intraepithelial neoplasia (disorder)", "Low grade cervical glandular intraepithelial neoplasia (diagnosis)", "cervical squamous cell intraepithelial glandular neoplasia low grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low grade cervical glandular intraepithelial neoplasia", "shortest_name_length": 54}
{"curie": "UMLS:C4521806", "names": ["Stage IV Anal Cancer", "Stage IV Anal Cancer AJCC v8", "Stage IV Anal Carcinoma AJCC v8", "Stage IV Anal Canal and Perianal (Anal Margin) Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Anal Cancer AJCC v8", "shortest_name_length": 20}
{"curie": "MONDO:0014464", "names": ["DECRD", "dienoyl-CoA reductase deficiency", "DECR deficiency with hyperlysinemia", "2,4-dienoyl-CoA reductase deficiency", "2,4-DIENOYL-CoA REDUCTASE DEFICIENCY", "2,4-Dienoyl-CoA Reductase Deficiency", "2,4-Dienoyl-CoA reductase deficiency", "2,4-@DIENOYL-CoA REDUCTASE DEFICIENCY", "Deficiency of 2,4-dienoyl-CoA reductase", "2,4-alpha dienoyl-CoA reductase deficiency", "Deficiency of 2,4-dienoyl-coenzyme A reductase", "Deficiency of 2,4-dienoyl-coenzyme A reductase (disorder)", "Progressive encephalopathy with leukodystrophy due to DECR deficiency", "progressive encephalopathy with leukodystrophy due to DECR deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive encephalopathy with leukodystrophy due to DECR deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C0399496", "names": ["Orofacial Granulomatosis", "Orofacial granulomatosis", "Orofacial Granulomatoses", "Granulomatoses, Orofacial", "Granulomatosis, Orofacial", "OFG - Orofacial granulomatosis", "Orofacial granulomatosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Granulomatosis, Orofacial", "shortest_name_length": 24}
{"curie": "MONDO:0006033", "names": ["DIPG", "Pontine (DIPG)", "DIPG Brain Tumor", "DIPG Brain Tumors", "Brain Tumor, DIPG", "diffuse midline glioma", "infiltrative brainstem glioma", "Diffuse Intrinsic Pontine Glioma", "diffuse intrinsic pontine glioma", "Diffuse intrinsic pontine glioma", "DIPG, Diffuse Intrinsic Pontine Glioma", "DIPG - diffuse intrinsic pontine glioma", "Diffuse intrinsic pontine glioma (disorder)", "Diffuse intrinsic pontine glioma (diagnosis)", "Diffuse intrinsic pontine glioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diffuse intrinsic pontine glioma", "shortest_name_length": 4}
{"curie": "MONDO:0014281", "names": ["Chlc, susceptibility to", "CHLC, SUSCEPTIBILITY TO", "cholangiocarcinoma, susceptibility to", "CHOLANGIOCARCINOMA, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholangiocarcinoma, susceptibility to", "shortest_name_length": 23}
{"curie": "MONDO:0004920", "names": ["hydrocele"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hydrocele", "shortest_name_length": 9}
{"curie": "UMLS:C1336158", "names": ["Stage IIA Esophagus Adenocarcinoma", "Stage IIA Esophageal Adenocarcinoma", "Stage IIA Adenocarcinoma of Esophagus", "Stage IIA Adenocarcinoma of the Esophagus", "Stage IIA Esophageal Adenocarcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Esophageal Adenocarcinoma AJCC v7", "shortest_name_length": 34}
{"curie": "MONDO:0008506", "names": ["SYMPHALANGISM OF TOES", "symphalangism of toes", "Symphalangism of Toes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "symphalangism of toes", "shortest_name_length": 21}
{"curie": "MONDO:0018029", "names": ["factor XIII deficiency", "Factor XIII deficiency", "Factor XIII Deficiency", "factor XIII deficiency disease", "deficiency, Laki-Lorand factor", "Factor XIII deficiency disease", "congenital factor XIII deficiency", "Fibrin stabilising factor deficiency", "fibrin-stabilizing factor deficiency", "fibrin stabilizing factor deficiency", "Fibrin stabilizing factor deficiency", "Hereditary factor XIII deficiency disease", "Factor XIII deficiency disease (disorder)", "hereditary factor XIII deficiency disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital factor XIII deficiency", "shortest_name_length": 22}
{"curie": "MONDO:0019499", "names": ["monosomy X", "Monosomy X", "XO syndrome", "XO genotype", "XO Syndrome", "xo syndrome", "monosomy; X", "XO SYNDROME", "X; monosomy", "45X Syndrome", "45X syndrome", "45,X syndrome", "45, X syndrome", "Turner-Ullrich", "Karyotype 45,X", "45,X0 syndrome", "45,X0 Syndrome", "Morgagni-Turner", "Karyotype 45, X", "karyotype 45, X", "turner syndrome", "karyotype; 45,X", "TURNER SYNDROME", "Turner Syndrome", "Turner syndrome", "syndrome; Turner", "genital dwarfism", "Turners Syndrome", "Turner; syndrome", "ovarian dwarfism", "turner's syndrome", "TURNER'S SYNDROME", "DWARFISM, OVARIAN", "Turner's syndrome", "Turner's Syndrome", "Gonadal Dysgenesis", "gonadal dysgenesis", "monosomy X syndrome", "45,X/46,XX syndrome", "Turner syndrome, NOS", "Turner syndrome (TS)", "TURNER-VARNY SYNDROME", "Turner Varny syndrome", "X0 - Turner's syndrome", "chromosome XO syndrome", "TS - Turner's syndrome", "chromosome X monosomy X", "45,X Gonadal Dysgenesis", "45,X gonadal dysgenesis", "Ullrich-Turner Syndrome", "ULLRICH-TURNER SYNDROME", "Ullrich-Turner syndrome", "Ullrich Turner Syndrome", "pseudonuchal infantilism", "Turner-Albright syndrome", "Morgagni-Turner syndrome", "Syndrome, Ullrich-Turner", "45X0 - Turner's syndrome", "bonnevie-ullrich syndrome", "Bonnevie-Ullrich syndrome", "gonadal dysgenesis (45,X)", "Bonnevie-Ullrich Syndrome", "Turner syndrome (disorder)", "Turner syndrome (diagnosis)", "gonadal dysgenesis - Turner", "Gonadal dysgenesis - Turner", "gonadal dysgenesis syndrome", "primary ovarian insufficiency", "genital dwarfism, Turner type", "Schereshevkii Turner syndrome", "Ullrich-Turner syndrome (UTS)", "Shereshevskii-Turner syndrome", "Turner Syndrome (XO Syndrome)", "Turner syndrome karyotype 45,X", "gonadal dysgenesis Turner type", "ovarian short stature syndrome", "Turner's syndrome, unspecified", "Turner syndrome karyotype 45, X", "Pterygolymphangiectasia syndrome", "chromosome; anomaly, sex, Turner", "Morgagni-Turner-Albright syndrome", "Turner; sex chromosome abnormality", "Turner syndrome karyotype 45,X (diagnosis)", "anomaly; chromosomes, chromosomal, sex, Turner"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Turner syndrome", "shortest_name_length": 10}
{"curie": "MONDO:0002191", "names": ["syringoma", "Syringoma", "SYRINGOMA", "syringomas", "Syringomas", "Syringoma NOS", "Syringoma, NOS", "[M]Syringoma NOS", "benign syringoma", "Syringoma of skin", "syringoma of skin", "Eccrine Syringoma", "eccrine syringoma", "Syringoma of skin (disorder)", "syringoma of skin (diagnosis)", "Syringoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syringoma", "shortest_name_length": 9}
{"curie": "MONDO:0013042", "names": ["AHUS4", "aHUS4", "aHUS with B factor anomaly", "aHUS, susceptibility to, 4", "AHUS, SUSCEPTIBILITY TO, 4", "D-HUS with B factor anomaly", "atypical HUS with B factor anomaly", "susceptibility to atypical hemolytic uremic syndrome 4", "atypical hemolytic-uremic syndrome with B factor anomaly", "hemolytic uremic syndrome, atypical, susceptibility to, 4", "HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 4", "hemolytic uremic syndrome, atypical, susceptibility to, type 4", "hemolytic-uremic syndrome without diarrhea with B factor anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical hemolytic-uremic syndrome with B factor anomaly", "shortest_name_length": 5}
{"curie": "MONDO:0014968", "names": ["PEAMO", "ENCEPHALOPATHY, PROGRESSIVE, WITH AMYOTROPHY AND OPTIC ATROPHY", "encephalopathy, progressive, with amyotrophy and optic atrophy", "encephalopathy, progressive, with amyotrophy and optic atrophy; PEAMO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephalopathy, progressive, with amyotrophy and optic atrophy", "shortest_name_length": 5}
{"curie": "UMLS:C3897451", "names": ["Subacute Placental Infarct", "Subacute Placental Infarction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subacute Placental Infarction", "shortest_name_length": 26}
{"curie": "UMLS:C1561256", "names": ["Pelvic soft tissue necrosis", "necrosis soft tissue pelvis", "necrosis of pelvic soft tissue", "Pelvic Soft Tissue Necrotic Lesion", "necrosis of pelvic soft tissue (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pelvic soft tissue necrosis", "shortest_name_length": 27}
{"curie": "MONDO:0010307", "names": ["MRX73", "XLID73", "X-linked mental retardation 73", "mental retardation, X-linked 73", "Mental Retardation, X-Linked 73", "MENTAL RETARDATION, X-LINKED 73", "intellectual disability, X-linked 73", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 73", "non-syndromic X-linked intellectual disability 73", "mental retardation, X-linked 73, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 73", "shortest_name_length": 5}
{"curie": "MONDO:0000549", "names": ["neck neuroblastoma", "neuroblastoma of neck", "cervical neuroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical neuroblastoma", "shortest_name_length": 18}
{"curie": "MONDO:0005233", "names": ["nsclc", "NSCLC", "non-oat cell lung cancer", "Nonsmall cell lung cancer", "NONSMALL CELL LUNG CANCER", "nonsmall cell lung cancer", "Nonsmall Cell Lung Cancer", "cancer cell lung non small", "Non-Small Cell Lung Cancer", "Non-small cell lung cancer", "small non cell lung cancer", "lung cancer non-small cell", "LUNG CANCER NON SMALL CELL", "non small cell lung cancer", "lung cancer, nonsmall cell", "cancer cell lung non-small", "lung cancer non small cell", "non-small cell lung cancer", "Lung cancer, non-small cell", "cancer cells lung non small", "Non-Small-Cell Lung Carcinoma", "non-small cell lung carcinoma", "Non-Small Cell Lung Carcinoma", "lung carcinoma non small cell", "Non-small cell lung carcinoma", "lung non-small cell carcinoma", "Lung Non-Small Cell Carcinoma", "carcinoma cell lung non-small", "Non-Small Cell Cancer of Lung", "non small cell lung carcinoma", "carcinoma cell lung non small", "Non Small Cell Lung Carcinoma", "non-small cell cancer of lung", "Lung Carcinoma, Non-Small-Cell", "Non Small Cell Lung Cancer NOS", "Non-Small-Cell Lung Carcinomas", "Carcinoma, Non-Small Cell Lung", "Non-small cell lung cancer NOS", "Carcinoma, Non-Small-Cell Lung", "Carcinoma, Non Small Cell Lung", "Lung Carcinomas, Non-Small-Cell", "Carcinomas, Non-Small-Cell Lung", "Non-small cell lung cancer, NOS", "Non-Small Cell Carcinoma of Lung", "non-small cell carcinoma of lung", "Non-Small Cell Cancer of the Lung", "non-small cell cancer of the lung", "NSCLC - Non-small cell lung cancer", "NSCLC - non-small cell lung cancer", "NSCLC - Non-Small Cell Lung Cancer", "non-small cell carcinoma of the lung", "Non-Small Cell Carcinoma of the Lung", "Non-small cell lung cancer (disorder)", "non-small cell lung carcinoma (disease)", "non-small cell carcinoma of lung (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-small cell lung carcinoma", "shortest_name_length": 5}
{"curie": "UMLS:C2721740", "names": ["Ventilation perfusion mismatch"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ventilation perfusion mismatch", "shortest_name_length": 30}
{"curie": "MONDO:0023415", "names": ["Congenital candidosis", "congenital candidiasis", "Congenital candidiasis", "Congenital Candidiasis", "congenital; candidiasis", "candidiasis; congenital", "Congenital candidiasis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital candidiasis", "shortest_name_length": 21}
{"curie": "MONDO:0004364", "names": ["choroid necrotic melanoma", "necrotic choroid melanoma", "Necrotic Choroid Melanoma", "Choroid Necrotic Melanoma", "necrotic Choroid melanoma", "necrotic melanoma of choroid", "Necrotic Melanoma of Choroid", "Necrotic Melanoma of the Choroid", "necrotic melanoma of the choroid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choroid necrotic melanoma", "shortest_name_length": 25}
{"curie": "MONDO:0002424", "names": ["Rectosigmoid Cancer", "rectosigmoid cancer", "Rectosigmoid cancer", "Rectosigmoid Carcinoma", "rectosigmoid carcinoma", "Rectosigmoid cancer NOS", "rectosigmoid junction carcinoma", "rectum; carcinoma, with sigmoid", "carcinoma of rectosigmoid junction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rectosigmoid carcinoma", "shortest_name_length": 19}
{"curie": "UMLS:C1336493", "names": ["stage I urethra cancer", "urethra cancer stage I", "Urethra Cancer Stage I", "Stage I Urethra Cancer", "Stage I Urethral Cancer", "stage I urethral cancer", "Stage I Urethra Carcinoma", "stage I urethra carcinoma", "Stage I Urethral Carcinoma", "stage I urethral carcinoma", "stage I carcinoma of urethra", "Stage I Carcinoma of Urethra", "stage I urethral cancer AJCC v7", "Stage I Urethral Cancer AJCC v7", "stage I carcinoma of the urethra", "Stage I Carcinoma of the Urethra"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Urethral Cancer AJCC v7", "shortest_name_length": 22}
{"curie": "MONDO:0009626", "names": ["BLCPMG", "PTORCH1", "BLC-PMG", "PSEUDO-TORCH SYNDROME", "Pseudo-TORCH syndrome", "pseudo-TORCH syndrome", "pseudo-TORCH syndrome 1", "Baraitser-Reardon syndrome", "Baraitser Brett Piesowicz syndrome", "Baraitser-Brett-Piesowicz syndrome", "microcephaly intracranial calcification", "Microcephaly intracranial calcification", "Congenital intrauterine infection-like syndrome", "congenital intrauterine infection-like syndrome", "bilateral band-like calcification with polymicrogyria", "Bilateral band-like calcification with polymicrogyria", "Congenital intrauterine infection-like syndrome (disorder)", "BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA", "microcephaly - intracranial calcification - intellectual disability", "band-like calcification with simplified gyration and polymicrogyria", "Microcephaly-intracranial calcification-intellectual disability syndrome", "microcephaly-intracranial calcification-intellectual disability syndrome", "Microcephaly, intracranial calcification, intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudo-TORCH syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C5447324", "names": ["Predominantly Antibody Deficiencies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Predominantly Antibody Deficiencies", "shortest_name_length": 35}
{"curie": "UMLS:C0021447", "names": ["Inguinal Hernia without Mention of Obstruction or Gangrene", "Inguinal hernia, without mention of obstruction or gangrene"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Inguinal hernia, without mention of obstruction or gangrene", "shortest_name_length": 58}
{"curie": "UMLS:C1336363", "names": ["Stage IVB Bone Sarcoma", "Stage IVB Sarcoma of Bone", "Stage IVB Sarcoma of the Bone", "Stage IVB Bone Sarcoma AJCC v7", "Stage IVB Bone Sarcoma  AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Bone Sarcoma AJCC v7", "shortest_name_length": 22}
{"curie": "UMLS:C1707372", "names": ["chemotherapeutic agent toxicity", "Chemotherapeutic Agent Toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chemotherapeutic Agent Toxicity", "shortest_name_length": 31}
{"curie": "UMLS:C4330255", "names": ["HNF1A-Associated Hyperinsulinism", "Hepatocyte Nuclear Factor 1-Alpha Hyperinsulinism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatocyte Nuclear Factor 1-Alpha Hyperinsulinism", "shortest_name_length": 32}
{"curie": "MONDO:0006115", "names": ["blast phase", "Blast Phase", "Blast crisis", "phase, blast", "BLAST CRISIS", "blast crises", "Blast Crises", "Phase, Blast", "blast crisis", "Blast Phases", "blast phases", "Blast Crisis", "Crisis, Blast", "Crises, Blast", "Phases, Blast", "crisis, blast", "crises, blast", "phases, blast", "blast phase CML", "Blast Phase CML", "blastic phase CML", "blastic phase CGL", "Blast cell crisis", "Blastic Phase CML", "CGL, blastic phase", "CML, blastic phase", "Blast crisis (qualifier value)", "blast phase chronic myeloid leukemia", "Blast Phase Chronic Myeloid Leukemia", "Blastic phase chronic myeloid leukemia", "Blastic Phase Chronic Myeloid Leukemia", "blastic phase chronic myeloid leukemia", "blast phase chronic myelocytic leukemia", "Blastic phase chronic myeloid leukaemia", "Blast Phase Chronic Myelocytic Leukemia", "blast phase chronic myelogenous leukemia", "Blast Phase Chronic Myelogenous Leukemia", "blastic phase chronic myelocytic leukemia", "Blast Phase Chronic Granulocytic Leukemia", "Blastic Phase Chronic Myelocytic Leukemia", "blast phase chronic granulocytic leukemia", "myelocytic leukemia, blastic phase chronic", "chronic myelocytic leukemia, blastic phase", "Blastic Phase Chronic Myelogenous Leukemia", "blastic phase chronic myelogenous leukemia", "blastic phase chronic granulocytic leukemia", "Blastic Phase Chronic Granulocytic Leukemia", "leukemia, blastic phase chronic myelogenous", "chronic myelogenous leukemia, blastic phase", "myelogenous leukemia, blastic phase chronic", "granulocytic leukemia, blastic phase chronic", "chronic granulocytic leukemia, blastic phase", "Blast crisis stage of chronic myeloid leukemia", "Blast crisis stage of chronic myeloid leukaemia", "Blastic phase chronic myeloid leukemia (disorder)", "blastic phase chronic myeloid leukemia (diagnosis)", "blast phase chronic myelogenous leukemia, BCR-ABL1 positive", "Blast Phase Chronic Myelogenous Leukemia, BCR-ABL1 Positive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blast phase chronic myelogenous leukemia, BCR-ABL1 positive", "shortest_name_length": 11}
{"curie": "UMLS:C0334398", "names": ["Malignant thecoma", "Thecoma, malignant", "Thecoma, Malignant", "thecoma; malignant", "malignant; thecoma", "Malignant Ovarian Thecoma", "Malignant Thecoma of Ovary", "malignant thecoma of ovary", "OVARIAN CANCER, THECA CELL", "THECOMA, OVARIAN, MALIGNANT", "Malignant Thecoma of the Ovary", "Malignant Ovarian Thecal Cell Tumor", "Malignant Thecal Cell Tumor of Ovary", "Malignant Ovarian Thecal Cell Neoplasm", "malignant thecoma of ovary (diagnosis)", "Malignant Thecal Cell Neoplasm of Ovary", "Malignant Thecal Cell Tumor of the Ovary", "Malignant Thecal Cell Neoplasm of the Ovary", "Thecoma, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Ovarian Thecoma", "shortest_name_length": 17}
{"curie": "UMLS:C5206866", "names": ["Peritoneal Epithelioid Mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peritoneal Epithelioid Mesothelioma", "shortest_name_length": 35}
{"curie": "UMLS:C1709465", "names": ["APT", "Atypical Parathyroid Tumor", "Atypical Parathyroid Neoplasm", "Atypical Parathyroid Gland Tumor", "Parathyroid Gland Atypical Adenoma", "Atypical Parathyroid Gland Adenoma", "Atypical Parathyroid Gland Neoplasm", "Parathyroid Tumor of Low/Uncertain Malignant Potential", "Parathyroid Gland Tumor of Low/Uncertain Malignant Potential"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypical Parathyroid Gland Tumor", "shortest_name_length": 3}
{"curie": "MONDO:0001649", "names": ["fungal esophagitis", "Fungal Esophagitis", "Fungal esophagitis", "Fungal oesophagitis", "Fungal esophagitis (disorder)", "fungal esophagitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fungal esophagitis", "shortest_name_length": 18}
{"curie": "MONDO:0012007", "names": ["SCIMITAR ANOMALY, MULTIPLE CARDIAC MALFORMATIONS, AND CRANIOFACIAL AND CENTRAL NERVOUS SYSTEM ABNORMALITIES", "Scimitar Anomaly, Multiple Cardiac Malformations, and Craniofacial and Central Nervous System Abnormalities", "scimitar anomaly, multiple cardiac malformations, and craniofacial and central nervous system abnormalities", "ANOMALOUS PULMONARY VENOUS RETURN, MULTIPLE CARDIAC MALFORMATIONS, AND CRANIOFACIAL AND CENTRAL NERVOUS SYSTEM ABNORMALITIES", "anomalous pulmonary Venous return, multiple Cardiac malformations, and craniofacial and central nervous system abnormalities", "Anomalous Pulmonary Venous Return, Multiple Cardiac Malformations, and Craniofacial and Central Nervous System Abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scimitar anomaly, multiple cardiac malformations, and craniofacial and central nervous system abnormalities", "shortest_name_length": 107}
{"curie": "UMLS:C2826104", "names": ["Myeloid Proliferations Related to Down Syndrome", "Myeloid Proliferations Associated with Down Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myeloid Proliferations Associated with Down Syndrome", "shortest_name_length": 47}
{"curie": "MONDO:0009864", "names": ["PCKDM", "PEPCK2", "PCK2 DEFICIENCY", "PCK2 deficiency", "PEPCK2 DEFICIENCY", "PEPCK2 deficiency", "PEPCK 2 deficiency", "PEPCK deficiency, mitochondrial", "phosphoenolpyruvate carboxykinase 2 deficiency", "Phosphoenolpyruvate carboxykinase 2 deficiency", "phosphoenolpyruvate carboxykinase deficiency, mitochondrial", "Phosphoenolpyruvate Carboxykinase Deficiency, Mitochondrial", "PHOSPHOENOLPYRUVATE CARBOXYKINASE DEFICIENCY, MITOCHONDRIAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phosphoenolpyruvate carboxykinase deficiency, mitochondrial", "shortest_name_length": 5}
{"curie": "UMLS:C1112789", "names": ["rectal spasm", "Rectal spasm", "rectal spasms"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rectal spasm", "shortest_name_length": 12}
{"curie": "UMLS:C0278689", "names": ["recurrent ovary cancer", "Relapsed ovarian cancer", "ovary cancer, recurrent", "Recurrent ovarian cancer", "Recurrent Ovarian Cancer", "Ovarian cancer recurrent", "ovarian cancer recurrent", "recurrent ovarian cancer", "ovarian cancer, recurrent", "Relapsed Ovarian Carcinoma", "recurrent ovarian carcinoma", "Recurrent Ovarian Carcinoma", "Relapsed Carcinoma of Ovary", "ovarian carcinoma, recurrent", "Recurrent Carcinoma of Ovary", "Relapsed Carcinoma of the Ovary", "Recurrent Carcinoma of the Ovary", "Relapsed Ovarian Epithelial Cancer", "Relapsed Epithelial Cancer of Ovary", "Recurrent Ovarian Epithelial Cancer", "recurrent ovarian epithelial cancer", "Ovarian epithelial cancer recurrent", "Recurrent ovarian cancer (disorder)", "Recurrent Epithelial Cancer of Ovary", "Recurrent ovarian cancer (diagnosis)", "ovarian epithelial cancer, recurrent", "Relapsed Epithelial Cancer of the Ovary", "Recurrent Epithelial Cancer of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent ovarian cancer", "shortest_name_length": 22}
{"curie": "UMLS:C4687704", "names": ["Malignant Pericardial Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Pericardial Germ Cell Tumor", "shortest_name_length": 37}
{"curie": "UMLS:C1535879", "names": ["Vessel puncture site bruise"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vessel puncture site bruise", "shortest_name_length": 27}
{"curie": "MONDO:0013566", "names": ["FANCL", "FANCL Fanconi anemia", "Fanconi anemia complementation group L", "FANCONI ANEMIA, COMPLEMENTATION GROUP L", "Fanconi anemia, complementation group L", "Fanconi Anemia, Complementation Group L", "Fanconi Anemia, complementation Group 50", "Fanconi anemia caused by mutation in FANCL", "Fanconi anemia complementation group type L", "Fanconi Anemia, complementation group type 50", "Fanconi anemia complementation group L (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fanconi anemia complementation group L", "shortest_name_length": 5}
{"curie": "UMLS:C5206482", "names": ["Metastatic Appendix Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Appendix Carcinoma", "shortest_name_length": 29}
{"curie": "UMLS:C5419867", "names": ["Low Grade PanIN", "Low-Grade PanIN", "Low-Grade Pancreatic Intraepithelial Neoplasia", "Low Grade Pancreatic Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Grade Pancreatic Intraepithelial Neoplasia", "shortest_name_length": 15}
{"curie": "MONDO:0042717", "names": ["Saul-Wilkes-Stevenson syndrome", "Saul Wilkes Stevenson syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Saul-Wilkes-Stevenson syndrome", "shortest_name_length": 30}
{"curie": "MONDO:0033620", "names": ["MFM10", "MYOFIBRILLAR MYOPATHY 10", "myofibrillar myopathy 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myofibrillar myopathy 10", "shortest_name_length": 5}
{"curie": "MONDO:0044305", "names": ["ECTD13", "ectodermal dysplasia 13", "ECTODERMAL DYSPLASIA 13, HAIR/TOOTH TYPE", "ectodermal dysplasia 13, hair/tooth type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia 13, hair/tooth type", "shortest_name_length": 6}
{"curie": "UMLS:C0855089", "names": ["Recurrent B-Cell Lymphoma", "B-cell lymphoma recurrent", "B-Cell Lymphoma Recurrent", "Recurrent B-Cell Non-Hodgkin Lymphoma", "B-cell non-Hodgkin's lymphoma recurrent", "Recurrent B-Cell Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-cell lymphoma recurrent", "shortest_name_length": 25}
{"curie": "MONDO:0019977", "names": ["Caribbean parkinsonism", "Atypical parkinsonism in the Caribbean", "parkinsonism with dementia of Guadeloupe", "Parkinsonism with dementia of Guadeloupe", "Parkinsonism with dementia of Guadeloupe (diagnosis)", "Parkinsonism co-occurrent with dementia of Guadeloupe", "Parkinsonism co-occurrent with dementia of Guadeloupe (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parkinsonism with dementia of Guadeloupe", "shortest_name_length": 22}
{"curie": "MONDO:0025419", "names": ["boils", "furuncle", "Furuncles", "Furunculosis", "Furunculoses", "FURUNCULOSIS", "furunculosis", "FORUNCULOSIS", "forunculosis", "Furunculosis NOS", "furunculosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "furunculosis", "shortest_name_length": 5}
{"curie": "MONDO:0008319", "names": ["epp", "EPP", "EPP1", "Protoporphyria", "protoporphyria", "magnus syndrome", "Magnus syndrome", "Magnus' syndrome", "Heme synthase deficiency", "Haem synthase deficiency", "ferrochelatase deficiency", "Hydroa aestivale syndrome", "Ferrochelatase Deficiency", "FERROCHELATASE DEFICIENCY", "Ferrochelatase deficiency", "Heme Synthetase Deficiency", "Deficiency, Ferrochelatase", "heme synthetase deficiency", "HEME SYNTHETASE DEFICIENCY", "protoporphyria (diagnosis)", "Ferrochelatase Deficiencies", "Deficiency, Heme Synthetase", "Synthetase Deficiency, Heme", "Deficiencies, Ferrochelatase", "Heme Synthetase Deficiencies", "erythrohepatic protoporphyria", "ERYTHROHEPATIC PROTOPORPHYRIA", "Erythrohepatic Protoporphyria", "Deficiencies, Heme Synthetase", "Erythrohepatic protoporphyria", "Erythropoietic Protoporphyria", "Erythropoietic protoporphyria", "erythropoietic protoporphyria", "Synthetase Deficiencies, Heme", "protoporphyria erythropoietic", "PROTOPORPHYRIA, ERYTHROPOIETIC", "Erythropoietic Protoporphyrias", "Protoporphyria, Erythropoietic", "Protoporphyria, erythropoietic", "protoporphyria; erythropoietic", "erythropoietic; protoporphyria", "protoporphyria, erythropoietic", "Protoporphyrias, Erythropoietic", "FECH - Ferrochelatase deficiency", "PROTOPORPHYRIA, ERYTHROPOIETIC, 1", "protoporphyria, erythropoietic, 1", "EPP - Erythropoietic protoporphyria", "Ferrochelatase deficiency (disorder)", "Autosomal erythropoietic protoporphyria", "Erythropoietic protoporphyria (disorder)", "erythropoietic protoporphyria (diagnosis)", "EPP (erythropoietic protoporphyria porphyria)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "protoporphyria, erythropoietic, 1", "shortest_name_length": 3}
{"curie": "UMLS:C4528220", "names": ["Primary Cutaneous Acral CD8-Positive T-Cell Lymphoma", "Primary cutaneous acral CD8 positive T-cell lymphoma", "Primary cutaneous acral CD8 positive T-cell lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary cutaneous acral CD8 positive T-cell lymphoma", "shortest_name_length": 52}
{"curie": "UMLS:C5555071", "names": ["Peripheral Chondrosarcoma, Grade 1", "Secondary Peripheral Chondrosarcoma, Grade 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary Peripheral Chondrosarcoma, Grade 1", "shortest_name_length": 34}
{"curie": "UMLS:C1334407", "names": ["Localized Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized Carcinoma", "shortest_name_length": 19}
{"curie": "MONDO:0009682", "names": ["MUSCULAR DYSTROPHY, CONGENITAL, WITH RAPID PROGRESSION", "Muscular Dystrophy, Congenital, with Rapid Progression", "muscular dystrophy, congenital, with rapid progression"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy, congenital, with rapid progression", "shortest_name_length": 54}
{"curie": "MONDO:0043472", "names": ["Ectopic ACTH syndrome", "ECTOPIC ACTH SYNDROME", "Ectopic ACTH Syndrome", "ectopic ACTH syndrome", "ectopia; ACTH syndrome", "ACTH Syndrome, Ectopic", "ectopic; ACTH syndrome", "syndrome; ectopic ACTH", "Syndrome, Ectopic ACTH", "Ectopic ACTH secretion", "Ectopic ACTH Secretion", "ACTH syndrome; ectopia", "ectopic ACTH secretion", "ACTH; ectopic syndrome", "Ectopic ACTH Syndromes", "ectopic ACTH syndromes", "syndrome, ectopic ACTH", "syndromes, ectopic ACTH", "ACTH syndromes, ectopic", "ACTH Syndromes, Ectopic", "Syndromes, Ectopic ACTH", "Ectopic Cushing syndrome", "Ectopic ACTH secreting tumor", "Occult ectopic ACTH secretion", "Ectopic corticotropin syndrome", "Paraneoplastic Cushing syndrome", "Ectopic corticotrophin syndrome", "ectopic ACTH secretion syndrome", "Ectopic ACTH Secretion Syndrome", "Cushing's syndrome due to ectopic ACTH", "hypercortisolism due to nonpituitary tumor", "Hypercortisolism due to nonpituitary tumor", "Hypercortisolism due to nonpituitary tumour", "Ectopic adrenocorticotropic hormone secretion", "Adrenocorticotropic hormone secretion syndrome", "Cushing syndrome due to ectopic ACTH secretion", "Ectopic ACTH secretion causing Cushing's syndrome", "ectopic ACTH secretion causing Cushing's syndrome", "Cushing's syndrome due to ectopic ACTH (diagnosis)", "Hypercortisolism due to nonpituitary tumor (disorder)", "Ectopic adrenocorticotropic hormone secretion (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectopic ACTH secretion syndrome", "shortest_name_length": 21}
{"curie": "MONDO:0011598", "names": ["ATOD4", "atopic dermatitis 4", "DERMATITIS, ATOPIC, 4", "dermatitis, ATOPIC, 4", "dermatitis, atopic, 4", "Dermatitis, Atopic, 4", "atopic dermatitis type 4", "dermatitis, atopic, susceptibility to, 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermatitis, atopic, 4", "shortest_name_length": 5}
{"curie": "UMLS:C2242683", "names": ["Gastroenteritis norovirus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastroenteritis norovirus", "shortest_name_length": 25}
{"curie": "UMLS:C4683584", "names": ["Lugano Classification Hodgkin Lymphoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Hodgkin Lymphoma by AJCC v8 Stage", "shortest_name_length": 55}
{"curie": "MONDO:0007281", "names": ["PCC", "CCA3", "CACA", "CTRCT4", "Frosted cataract", "Aculeiform cataract", "Cataract, Aculeiform", "Fasciculiform cataract", "Needle-shaped cataract", "CRYGD cataract (disease)", "cataract 4 multiple types", "cataract 4, multiple types", "CATARACT 4, MULTIPLE TYPES", "cataract, crystalline aculeiform", "Cataract, Crystalline Aculeiform", "CATARACT, CRYSTALLINE ACULEIFORM", "congenital cataract cerulean type 3", "Cataract, Congenital Blue Dot Type, 3", "CATARACT, CONGENITAL, CERULEAN TYPE, 3", "cataract, congenital, cerulean type, 3", "Cataract, Congenital, Cerulean Type, 3", "CATARACT, NONNUCLEAR POLYMORPHIC CONGENITAL", "cataract, Nonnuclear polymorphic congenital", "CATARACT, PUNCTATE, PROGRESSIVE JUVENILE-ONSET", "cataract (disease) caused by mutation in CRYGD", "cataract, punctate, progressive juvenile-onset", "Cataract, Punctate, Progressive Juvenile-Onset", "cataract 4 multiple types with or without microcornea", "CATARACT 4, MULTIPLE TYPES, WITH OR WITHOUT MICROCORNEA", "cataract 4, multiple types, with or without microcornea"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 4 multiple types", "shortest_name_length": 3}
{"curie": "MONDO:0007092", "names": ["AIH2", "AI1B", "ENAM amelogenesis imperfecta", "enam amelogenesis imperfecta", "amelogenesis imperfecta type 1B", "amelogenesis imperfecta type IB", "amelogenesis imperfecta, type 1B", "AMELOGENESIS IMPERFECTA, TYPE IB", "amelogenesis imperfecta, type IB", "Amelogenesis Imperfecta, Type IB", "hereditary localized enamel hypoplasia", "ENAMEL HYPOPLASIA, HEREDITARY LOCALIZED", "enamel hypoplasia, hereditary localized", "Enamel Hypoplasia, Hereditary Localized", "amelogenesis imperfecta caused by mutation in ENAM", "amelogenesis imperfecta caused by mutation in enam", "autosomal dominant hypoplastic local amelogenesis imperfecta", "AMELOGENESIS IMPERFECTA, HYPOPLASTIC LOCAL, AUTOSOMAL DOMINANT", "Amelogenesis Imperfecta, Hypoplastic Local, Autosomal Dominant", "amelogenesis imperfecta, hypoplastic local, autosomal dominant", "Amelogenesis imperfecta - hypoplastic autosomal dominant - local", "Amelogenesis imperfecta - hypoplastic autosomal dominant - local (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amelogenesis imperfecta type 1B", "shortest_name_length": 4}
{"curie": "MONDO:0014252", "names": ["FHBL", "FHBL1", "LDLCQ4", "hypobetalipoproteinemia", "APOB hypobetalipoproteinemia", "Familial hypobetalipoproteinemia", "familial hypobetalipoproteinemia", "hypobetalipoproteinemia, familial", "Familial hypobetalipoproteinaemia", "HYPOBETALIPOPROTEINEMIA, FAMILIAL", "familial hypobetalipoproteinemia 1", "Hypobetalipoproteinemia (familial)", "Hypobetalipoproteinemia, Familial, 1", "HYPOBETALIPOPROTEINEMIA, FAMILIAL, 1", "hypobetalipoproteinemia, familial, 1", "familial hypobetalipoproteinemia type 1", "hypobetalipoproteinemia, familial, type 1", "acanthocytosis with hypobetalipoproteinemia", "Acanthocytosis With Hypobetalipoproteinemia", "ACANTHOCYTOSIS WITH HYPOBETALIPOPROTEINEMIA", "Familial hypobetalipoproteinemia (disorder)", "familial hypobetalipoproteinemia (diagnosis)", "Hypobetalipoproteinemia, Normotriglyceridemic", "HYPOBETALIPOPROTEINEMIA, NORMOTRIGLYCERIDEMIC", "hypobetalipoproteinemia, Normotriglyceridemic", "hypobetalipoproteinemia caused by mutation in APOB", "LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial hypobetalipoproteinemia 1", "shortest_name_length": 4}
{"curie": "UMLS:C0079238", "names": ["Gastroenteric fistula", "Gastrointestinal fistula", "gastrointestinal fistula", "Gastrointestinal Fistula", "Digestive System Fistula", "Digestive System Fistulas", "fistulas gastrointestinal", "Gastrointestinal fistulae", "Fistula, Digestive System", "Fistulas, Digestive System", "Fistula of digestive system", "Gastrointestinal fistula, NOS", "Gastrointestinal fistula (disorder)", "gastrointestinal fistula (diagnosis)", "Fistula of digestive system (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Digestive System Fistula", "shortest_name_length": 21}
{"curie": "MONDO:0043291", "names": ["Aschoff-Rokitansky sinus", "Rokitansky-Aschoff Sinus", "Aschoff-Rokitansky sinuses", "Rokitansky-Aschoff sinuses", "Aschoff-Rokitansky sinuses (disorder)", "intramural diverticulosis of the gallbladder", "Intramural diverticulosis of the gallbladder", "Rokitansky-Aschoff sinuses of the gallbladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rokitansky-Aschoff sinuses of the gallbladder", "shortest_name_length": 24}
{"curie": "MONDO:0015355", "names": ["dHMN7", "DHMNVPy", "distal hereditary motor neuropathy type 7", "distal hereditary motor neuronopathy type 7", "distal spinal muscular atrophy with vocal cord paralysis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal hereditary motor neuropathy type 7", "shortest_name_length": 5}
{"curie": "MONDO:0009517", "names": ["Donohue", "LEPRECHAUNISM", "Leprechaunism", "leprechaunism", "Leprechaunisms", "Donohue Syndrome", "donohue syndrome", "Donohue syndrome", "DONOHUE SYNDROME", "Syndrome, Donohue", "Donohue's syndrome", "Donahue's syndrome", "donohue's syndrome", "donahue's syndrome", "leprechaunism syndrome", "Leprechaunism syndrome", "Insulin receptor defect", "insulin receptor, defect 1N", "Insulin Receptor, Defect in", "INSULIN RECEPTOR, DEFECT IN", "Insulin receptor defect, NOS", "Leprechaunism syndrome (disorder)", "Insulin receptor defect (disorder)", "Leprechaunism syndrome (diagnosis)", "congenital malformation syndromes Leprechaunism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Donohue syndrome", "shortest_name_length": 7}
{"curie": "UMLS:C0862489", "names": ["Metastatic Endometrial Adenocarcinoma", "Endometrial adenocarcinoma metastatic", "Adenocarcinoma endometrial metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma endometrial metastatic", "shortest_name_length": 37}
{"curie": "MONDO:0100146", "names": ["ATP6AP2-related disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ATP6AP2-related disorder", "shortest_name_length": 24}
{"curie": "UMLS:C5205619", "names": ["Platinum-Sensitive Peritoneal Cancer", "Platinum-Sensitive Peritoneal Carcinoma", "Platinum-Sensitive Primary Peritoneal Cancer", "Platinum-Sensitive Primary Peritoneal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Platinum-Sensitive Primary Peritoneal Carcinoma", "shortest_name_length": 36}
{"curie": "MONDO:0005348", "names": ["Keloid", "keloid", "KELOID", "cheloid", "Cheloid", "keloids", "Keloids", "cheloids", "keloid skin", "Keloid scar", "scar keloid", "keloid scar", "keloids skin", "keloid scars", "scar; keloid", "keloid; scar", "keloids scars", "Keloid of skin", "Keloid Process", "Keloid scarring", "Cheloid of skin", "Keloid cicatrix", "keloid scarring", "Keloid scar of skin", "keloid skin disorder", "Keloid scar (disorder)", "keloid scar (diagnosis)", "Keloid (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keloid", "shortest_name_length": 6}
{"curie": "UMLS:C1274933", "names": ["Drug Induced Stevens Johnson Syndrome", "Drug-Induced Stevens Johnson Syndrome", "Drug-Induced Stevens-Johnson Syndrome", "Drug-induced Stevens-Johnson syndrome", "Drug-Induced Stevens-Johnson Syndromes", "Stevens-Johnson Syndrome, Drug-Induced", "Stevens-Johnson syndrome caused by drug", "Stevens-Johnson Syndromes, Drug-Induced", "Stevens-Johnson syndrome caused by drug (disorder)", "Stevens-Johnson syndrome caused by drug (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drug-Induced Stevens Johnson Syndrome", "shortest_name_length": 37}
{"curie": "MONDO:0000980", "names": ["aortic sclerosis", "atherosclerosis aorta", "aorta atherosclerosis", "Atherosclerosis aorta", "AORTA ATHEROSCLEROSIS", "aortic atherosclerosis", "Aortic atherosclerosis", "atherosclerosis of aorta", "Atherosclerosis of aorta", "Atherosclerosis of the aorta", "Aortic atherosclerotic lesion", "Plaque build-up in aorta artery", "Atherosclerotic changes of aorta", "aortic atherosclerosis (disease)", "Atherosclerosis of aorta (disorder)", "atherosclerosis of aorta (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic atherosclerosis", "shortest_name_length": 16}
{"curie": "UMLS:C1336134", "names": ["stage IB gastric cancer", "Gastric Cancer Stage IB", "gastric cancer stage IB", "Stage IB Gastric Cancer", "Gastric Carcinoma Stage IB", "stage IB stomach carcinoma", "Stomach Carcinoma Stage IB", "stomach carcinoma stage IB", "gastric carcinoma stage IB", "Stage IB Stomach Carcinoma", "stage IB gastric carcinoma", "Stage IB Gastric Carcinoma", "Stage IB Carcinoma of Stomach", "stage IB carcinoma of stomach", "carcinoma of stomach stage IB", "Carcinoma of Stomach Stage IB", "stage IB gastric cancer AJCC v7", "Stage IB Gastric Cancer AJCC v7", "Stage IB Gastric (Stomach) Cancer", "Carcinoma of the Stomach Stage IB", "carcinoma of the stomach stage IB", "Stage IB Carcinoma of the Stomach", "stage IB carcinoma of the stomach"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Gastric Carcinoma", "shortest_name_length": 23}
{"curie": "MONDO:0100359", "names": ["herpes simplex type 1 infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "herpes simplex type 1 infectious disease", "shortest_name_length": 40}
{"curie": "MONDO:0017160", "names": ["bv-FTD", "Frontotemporal dementia, behavioral variant", "frontotemporal dementia behavioral variant of", "Behavioral variant of frontotemporal dementia", "behavioral variant of frontotemporal dementia", "Behavioural variant of frontotemporal dementia", "Behavioral variant of frontotemporal dementia (disorder)", "Behavioral variant of frontotemporal dementia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "behavioral variant of frontotemporal dementia", "shortest_name_length": 6}
{"curie": "MONDO:0022942", "names": ["deafness mesenteric diverticula of small bowel neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness mesenteric diverticula of small bowel neuropathy", "shortest_name_length": 57}
{"curie": "UMLS:C4520718", "names": ["Stage I Rectal Cancer", "Rectal Cancer Stage I", "Dukes A Rectal Carcinoma", "Stage I Rectal Carcinoma", "AJCC Stage I Rectal Cancer", "Stage I Carcinoma of Rectum", "Dukes A Carcinoma of Rectum", "Stage I Rectal Cancer AJCC v7", "Stage I Rectal Cancer AJCC v6", "Stage I Carcinoma of the Rectum", "Dukes A Carcinoma of the Rectum", "Stage I Rectal Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Rectal Cancer AJCC v6 and v7", "shortest_name_length": 21}
{"curie": "MONDO:0000181", "names": ["microcephaly and chorioretinopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly and chorioretinopathy", "shortest_name_length": 34}
{"curie": "MONDO:0001906", "names": ["Lens in posterior chamber", "posterior dislocation of lens", "Posterior dislocation of lens", "Posterior dislocation of lens (disorder)", "posterior dislocation of lens (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "posterior dislocation of lens", "shortest_name_length": 25}
{"curie": "UMLS:C4721665", "names": ["Stage 0 Esophageal Squamous Cell Cancer", "Esophagus Squamous Cell Carcinoma in situ", "Stage 0 Esophagus Squamous Cell Carcinoma", "Esophageal Squamous Cell Carcinoma Stage 0", "Esophageal Squamous Cell Carcinoma in situ", "Stage 0 Esophageal Squamous Cell Carcinoma", "Oesophageal Squamous Cell Carcinoma Stage 0", "Stage 0 Squamous Cell Carcinoma of Esophagus", "Squamous Cell Carcinoma in situ of Esophagus", "Stage 0 Squamous Cell Carcinoma of the Esophagus", "Squamous Cell Carcinoma in situ of the Esophagus", "Stage 0 Esophageal Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Esophageal Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 39}
{"curie": "UMLS:C0265152", "names": ["PERICARDITIS UREMIC", "Pericarditis uremic", "Uremic pericarditis", "uremic pericarditis", "Uremic Pericarditis", "Uraemic pericarditis", "Pericarditis uraemic", "uremic pericarditis (diagnosis)", "Pericarditis secondary to uremia", "Pericarditis secondary to uraemia", "Pericarditis co-occurrent and due to uremia", "Pericarditis co-occurrent and due to uraemia", "Pericarditis co-occurrent and due to uremia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pericarditis secondary to uremia", "shortest_name_length": 19}
{"curie": "UMLS:C5401417", "names": ["Metastatic Anal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Anal Carcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0025003", "names": ["Goat Disease", "goat disease", "disease, goat", "Disease, Goat", "Goat Diseases", "diseases, goat", "Diseases, Goat", "caprine disease", "Caprine Disease", "Goats--Diseases", "caprine diseases", "Disease, Caprine", "Caprine Diseases", "disease, caprine", "Diseases, Caprine", "diseases, caprine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "goat disease", "shortest_name_length": 12}
{"curie": "MONDO:0000993", "names": ["PRSC", "Prostate Squamous Cell Carcinoma", "prostate squamous cell carcinoma", "squamous cell carcinoma of prostate", "Squamous Cell Carcinoma of Prostate", "Squamous cell carcinoma of prostate", "prostate gland squamous cell carcinoma", "Squamous Cell Carcinoma of the Prostate", "squamous cell carcinoma of the prostate", "squamous cell carcinoma of prostate gland", "Squamous cell carcinoma of prostate (disorder)", "squamous cell carcinoma of prostate gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate squamous cell carcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0004191", "names": ["Nephrogenic Adenoma", "nephrogenic adenoma", "Nephrogenic adenoma", "Nephrogenic Metaplasia", "Nephrogenic metaplasia", "Nephrogenic metaplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrogenic adenoma", "shortest_name_length": 19}
{"curie": "UMLS:C0270934", "names": ["toxic neuropathy", "neuropathy toxic", "Toxic neuropathy", "neuropathy; toxic", "neuropathies toxic", "Toxic polyneuropathy", "Toxic Polyneuropathy", "toxic polyneuropathy", "Polyneuropathy toxic", "Toxic neuropathy, NOS", "neuropathy peripheral toxic", "polyneuropathy; toxic agent", "toxic; agent, polyneuropathy", "Toxic polyneuropathy (disorder)", "toxic polyneuropathy (diagnosis)", "Polyneuropathy due to toxic agents", "Polyneuropathy due to toxic agents, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Toxic polyneuropathy", "shortest_name_length": 16}
{"curie": "UMLS:C4553670", "names": ["Stage IIIB Uterine Corpus Cancer AJCC v8", "Stage IIIB Uterine (including Endometrial) Cancer", "Stage IIIB Uterine Corpus Carcinoma or Carcinosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Uterine Corpus Cancer AJCC v8", "shortest_name_length": 40}
{"curie": "UMLS:C1853925", "names": ["Spondyloocular Syndrome, Autosomal Recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spondyloocular Syndrome, Autosomal Recessive", "shortest_name_length": 44}
{"curie": "MONDO:0100144", "names": ["Uner Tan Syndrome", "recessive quadrupedalism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uner Tan Syndrome", "shortest_name_length": 17}
{"curie": "MONDO:0013033", "names": ["CPSQ2", "KANK1 spastic quadriplegia", "spastic quadriplegic cerebral palsy 2", "Cerebral Palsy, Spastic Quadriplegic, 2", "CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 2", "cerebral palsy, spastic quadriplegic, 2", "cerebral palsy, spastic quadriplegic, type 2", "spastic quadriplegia caused by mutation in KANK1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral palsy, spastic quadriplegic, 2", "shortest_name_length": 5}
{"curie": "MONDO:0001736", "names": ["Neonatal infective mastitis", "neonatal infective mastitis", "mastitis; neonatal infective", "mastitis; infective, newborn", "Neonatal infective mastitis (disorder)", "neonatal infective mastitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal infective mastitis", "shortest_name_length": 27}
{"curie": "MONDO:0013386", "names": ["DFNB74", "autosomal recessive deafness 74", "DEAFNESS, AUTOSOMAL RECESSIVE 74", "deafness, autosomal recessive 74", "deafness, autosomal recessive type 74", "autosomal recessive nonsyndromic deafness 74", "MSRB3 autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 74", "autosomal recessive nonsyndromic deafness type 74", "autosomal recessive nonsyndromic deafness caused by mutation in MSRB3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 74", "shortest_name_length": 6}
{"curie": "MONDO:0016802", "names": ["mitochondrial protein import disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial protein import disorder", "shortest_name_length": 37}
{"curie": "UMLS:C4049701", "names": ["FRNS", "Frequently Relapsing Nephrotic Syndrome", "Nephrotic Syndrome - Frequently Relapsing"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - Frequently Relapsing", "shortest_name_length": 4}
{"curie": "UMLS:C3272633", "names": ["Hyaline Arteriolosclerosis", "Hyaline arteriolosclerosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyaline arteriolosclerosis", "shortest_name_length": 26}
{"curie": "MONDO:0021228", "names": ["Brainstem Tumor", "brainstem tumor", "brain stem tumor", "Brain Stem Tumor", "Brainstem Neoplasm", "tumor of brainstem", "brainstem neoplasm", "Tumor of Brainstem", "tumor of brain stem", "Tumor of Brain Stem", "brain stem neoplasm", "Brain Stem Neoplasm", "Brain stem neoplasm", "Neoplasm of Brainstem", "neoplasm of brainstem", "tumor of the brainstem", "neoplasm of brain stem", "Tumor of the Brainstem", "Neoplasm of Brain Stem", "Tumor of the Brain Stem", "tumor of the brain stem", "Neoplasm of the Brainstem", "neoplasm of the brainstem", "Neoplasm of the Brain Stem", "neoplasm of the brain stem", "brainstem neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brainstem neoplasm", "shortest_name_length": 15}
{"curie": "MONDO:0012345", "names": ["PSS2", "APSS", "Acral PSS", "acral PSS", "localized PSS", "Localized PSS", "acral deciduous skin", "Acral deciduous skin", "PEELING SKIN SYNDROME 2", "Peeling skin syndrome 2", "peeling skin syndrome 2", "Localized deciduous skin", "localized deciduous skin", "ACRAL PEELING SKIN SYNDROME", "acral peeling skin syndrome", "Acral peeling skin syndrome", "peeling skin syndrome type 2", "PEELING SKIN SYNDROME, ACRAL TYPE", "peeling skin syndrome, acral type", "Peeling skin syndrome, acral type", "Acral peeling skin syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acral peeling skin syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0021271", "names": ["colon villous adenoma", "Colon Villous Adenoma", "Colonic Villous Adenoma", "COLON, ADENOMA, VILLOUS", "Colonic villous adenoma", "colonic villous adenoma", "Villous Adenoma of Colon", "Villous adenoma of colon", "villous adenoma of colon", "COLON, ADENOMA, PAPILLARY", "Villous Adenoma of the Colon", "villous adenoma of the colon", "Villous adenoma of colon (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "villous adenoma of colon", "shortest_name_length": 21}
{"curie": "MONDO:0000963", "names": ["esophagus lipoma", "esophageal lipoma", "Esophageal Lipoma", "Lipoma of esophagus", "lipoma of esophagus", "Lipoma of Esophagus", "Lipoma of the Esophagus", "lipoma of the esophagus", "lipoma of esophagus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophageal lipoma", "shortest_name_length": 16}
{"curie": "MONDO:0001517", "names": ["dysentery", "Dysentery", "dysyntery", "DYSENTERY", "dysenteries", "Dysentery NOS", "Dysentery, NOS", "infective diarrhea", "Infective diarrhea", "Infective diarrhoea", "Diarrhea infectious", "dysenteric diarrhea", "Infectious diarrhea", "infectious diarrhea", "infectious; diarrhea", "Diarrhoea infectious", "diarrhea; infectious", "infectious diarrhoea", "Infectious diarrhoea", "Dysentery (diagnosis)", "Infectious Diarrheal Disease", "Infectious diarrheal disease", "infectious diarrheal disease", "infectious diarrheal diseases", "Infectious Diarrheal Diseases", "Diarrheal Disease, Infectious", "Infectious diarrhoeal disease", "diarrheal disease, infectious", "intestinal infections dysentery", "infectious diarrhea (diagnosis)", "Infectious diarrheal disease NOS", "Infectious diarrheal disease, NOS", "Infectious diarrhoeal disease, NOS", "Infectious diarrheal disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dysentery", "shortest_name_length": 9}
{"curie": "MONDO:0043137", "names": ["isolated microcephaly", "nonsyndromic microcephaly", "Microcephaly nonsyndromal", "Nonsyndromal microcephaly", "Nonsyndromic microcephaly", "microcephaly, non-syndromic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated microcephaly", "shortest_name_length": 21}
{"curie": "UMLS:C0161010", "names": ["foreign body throat", "pharynx foreign body", "foreign body; throat", "bodies foreign throat", "foreign body; pharynx", "foreign body in throat", "Foreign body in throat", "Pharyngeal foreign body", "pharyngeal foreign body", "foreign body in pharynx", "Foreign body in pharynx", "foreign body of pharynx", "body foreign pharyngeal", "foreign body pharyngeal", "Foreign body (in);throat", "Foreign body (in);pharynx", "Foreign body in throat NOS", "Foreign body in throat, NOS", "Pharyngeal FB - foreign body", "Foreign body in pharynx (disorder)", "foreign body of pharynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Foreign body in pharynx", "shortest_name_length": 19}
{"curie": "MONDO:0044921", "names": ["Atypical Lymphoid Hyperplasia", "atypical lymphoid hyperplasia", "Atypical lymphoid hyperplasia", "atypical lymphoproliferative disorder", "Atypical lymphoproliferative disorder", "Atypical Lymphoproliferative Disorder", "Atypical lymphoproliferative disorder, NOS", "Atypical lymphoproliferative disorder (disorder)", "Atypical lymphoid hyperplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical lymphoproliferative disorder", "shortest_name_length": 29}
{"curie": "UMLS:C4728118", "names": ["Rebound acid hypersecretion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rebound acid hypersecretion", "shortest_name_length": 27}
{"curie": "MONDO:0010974", "names": ["SRN1", "NPHS2", "NPHS2 nephrotic syndrome", "nephrotic syndrome type 2", "nephrotic syndrome, type 2", "nephrotic syndrome caused by mutation in NPHS2", "nephrotic syndrome, idiopathic, steroid-resistant", "steroid-resistant autosomal recessive nephrotic syndrome", "nephrotic syndrome, steroid-resistant, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrotic syndrome, type 2", "shortest_name_length": 4}
{"curie": "UMLS:C1504383", "names": ["Radiation skin injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radiation skin injury", "shortest_name_length": 21}
{"curie": "MONDO:0013871", "names": ["SCKL6", "Seckel syndrome 6", "SECKEL SYNDROME 6", "CEP63 Seckel syndrome", "Seckel syndrome type 6", "Seckel syndrome caused by mutation in CEP63"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Seckel syndrome 6", "shortest_name_length": 5}
{"curie": "MONDO:0002778", "names": ["Epidural Spinal Canal Meningioma", "epidural spinal canal meningioma", "Meningioma of Epidural Spinal Canal", "meningioma of epidural spinal canal", "Meningioma of the Epidural Spinal Canal", "meningioma of the epidural spinal canal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidural spinal canal meningioma", "shortest_name_length": 32}
{"curie": "UMLS:C4727169", "names": ["Metastatic Gastric Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Gastric Carcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0010695", "names": ["occipital hair, white lock of", "OCCIPITAL HAIR, WHITE LOCK OF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "occipital hair, white lock of", "shortest_name_length": 29}
{"curie": "UMLS:C0334305", "names": ["adenocarcinoma in villous adenoma", "Adenocarcinoma in villous adenoma", "Adenocarcinoma in Villous Adenoma", "Adenocarcinoma in villous adenoma (disorder)", "adenocarcinoma in villous adenoma (diagnosis)", "Adenocarcinoma in villous adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma in villous adenoma", "shortest_name_length": 33}
{"curie": "MONDO:0030703", "names": ["autoimmune vasculitis", "Autoimmune vasculitis", "Immune mediated vasculitis", "Autoimmune vasculitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune vasculitis", "shortest_name_length": 21}
{"curie": "MONDO:0006355", "names": ["parotid acinic cell carcinoma", "Parotid Acinic Cell Carcinoma", "acinic cell carcinoma of parotid", "Acinic Cell Carcinoma of Parotid", "parotid gland acinic cell carcinoma", "Parotid Gland Acinic Cell Carcinoma", "parotid gland acinar cell carcinoma", "Acinic Cell Carcinoma of the Parotid", "acinic cell carcinoma of the parotid", "Acinic Cell Carcinoma of Parotid Gland", "acinic cell carcinoma of parotid gland", "acinic cell carcinoma of the parotid gland", "Acinic Cell Carcinoma of the Parotid Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parotid gland acinic cell carcinoma", "shortest_name_length": 29}
{"curie": "UMLS:C0008629", "names": ["Chromosome Fragility", "Chromosomal Fragility", "Fragility, Chromosome", "Fragility, Chromosomal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chromosome Fragility", "shortest_name_length": 20}
{"curie": "UMLS:C4330627", "names": ["Major Salivary Gland Cancer by AJCC v8 Stage", "Major Salivary Gland Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Major Salivary Gland Cancer by AJCC v8 Stage", "shortest_name_length": 44}
{"curie": "MONDO:0001071", "names": ["mr", "Low intelligence", "Deficiency mental", "MENTAL DEFICIENCY", "Dull intelligence", "Deficiency;mental", "Mental deficiency", "DEFICIENCY MENTAL", "mental deficiency", "Mental Deficiency", "RETARDATION MENTAL", "MENTAL RETARDATION", "Mental retardation", "Deficiency, Mental", "Retardation;mental", "mental retardation", "Retardation mental", "Mental Retardation", "Mental-retardation", "mental retardations", "mental deficiencies", "Mental Deficiencies", "Retardation, Mental", "Deficiencies, Mental", "Retardation (Mental)", "Mental deficiency NOS", "poor school performance", "Intellectual limitation", "Mental retardation, NOS", "Poor school performance", "Disability;intellectual", "Intellectual Disability", "MR - Mental retardation", "Intellectual disability", "disability intellectual", "intellectual disability", "Disability, Intellectual", "Intellectual Disabilities", "disabilities intellectual", "Intellectual disabilities", "INTELLECTUAL DISABILITIES", "intellectual disabilities", "Low intelligence (finding)", "Disabilities, Intellectual", "mental retardation diagnosis", "Unspecified mental retardation", "Mental retardation, nonspecific", "Intellectual Development Disorder", "poor school performance (symptom)", "Nonprogressive mental retardation", "Intellectual development disorder", "Intellectual disability (disorder)", "Intellectual Development Disorders", "Disorder, Intellectual Development", "Development Disorder, Intellectual", "Development Disorders, Intellectual", "intellectual disabilities (history)", "Intellectual developmental disorder", "Intellectual functioning disability", "Disorders, Intellectual Development", "intellectual; developmental disorder", "developmental disorder; intellectual", "intellectual disabilities (diagnosis)", "Nonprogressive intellectual disability", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15", "Intellectual functioning disability (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability", "shortest_name_length": 2}
{"curie": "UMLS:C0162628", "names": ["viral skin disease", "Viral Skin Disease", "skin disease viral", "Disease, Viral Skin", "Skin Disease, Viral", "viral skin diseases", "Viral Skin Diseases", "Skin Diseases, Viral", "Viral skin infection", "Diseases, Viral Skin", "skin viral infection", "viral skin infection", "infections skin viral", "viral infection of skin", "Viral infection of skin", "Viral dermatological disorders", "Viral infection of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin Diseases, Viral", "shortest_name_length": 18}
{"curie": "MONDO:0015209", "names": ["isolated gastroduodenal malformation", "nonsyndromic gastroduodenal malformation", "non-syndromic gastroduodenal malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-syndromic gastroduodenal malformation", "shortest_name_length": 36}
{"curie": "MONDO:0045072", "names": ["neoplasm associated ectopic hormone secretion syndrome", "Neoplasm Associated Ectopic Hormone Secretion Syndrome", "Ectopic Hormone Secretion Syndrome Associated with Neoplasia", "ectopic hormone secretion syndrome associated with neoplasia", "Ectopic hormone secretion syndromes associated with neoplasias"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectopic hormone secretion syndrome associated with neoplasia", "shortest_name_length": 54}
{"curie": "MONDO:0012408", "names": ["MCOPCB3", "microphthalmia with coloboma 3", "microphthalmia, colobomatous, isolated 3", "MICROPHTHALMIA, COLOBOMATOUS, ISOLATED 3", "Microphthalmia, Colobomatous, Isolated 3", "MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 3", "Microphthalmia, Isolated, with Coloboma 3", "microphthalmia, isolated, with coloboma 3", "VSX2 microphthalmia, isolated, with coloboma", "microphthalmia, isolated, with coloboma type 3", "Microphthalmia, Cataracts, and Iris Abnormalities", "MICROPHTHALMIA, CATARACTS, AND IRIS ABNORMALITIES", "microphthalmia, cataracts, and iris abnormalities", "microphthalmia, isolated, with coloboma caused by mutation in VSX2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microphthalmia, isolated, with coloboma 3", "shortest_name_length": 7}
{"curie": "MONDO:0023693", "names": ["MSUD2", "MSUD type 2", "maple syrup urine disease type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maple syrup urine disease type 2", "shortest_name_length": 5}
{"curie": "UMLS:C4525102", "names": ["Colon Cancer by AJCC v8 Stage", "Colon Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colon Cancer by AJCC v8 Stage", "shortest_name_length": 29}
{"curie": "UMLS:C0038219", "names": ["Status Dysraphicus", "status dysraphicus", "Dysraphicus, Status"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Status Dysraphicus", "shortest_name_length": 18}
{"curie": "MONDO:0003572", "names": ["Schminke tumor", "Schmincke tumor", "Schmincke Tumor", "Schminke tumour", "Lymphepithelioma", "Lymphoepithelioma", "lymphoepithelioma", "lymphoepithelial carcinoma", "Lymphoepithelial carcinoma", "Lymphoepithelial Carcinoma", "Lymphoepithelial-like carcinoma", "Lymphoepithelioma-like carcinoma", "lymphoepithelioma-like carcinoma", "Lymphoepithelioma-Like Carcinoma", "Lymphoepithelial carcinoma (disorder)", "lymphoepithelial carcinoma (diagnosis)", "Nasopharyngeal type Undifferentiated carcinoma", "Nasopharyngeal Type Undifferentiated Carcinoma", "Nasopharyngeal-Type Undifferentiated Carcinoma", "nasopharyngeal type undifferentiated carcinoma", "Lymphoepithelial carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasopharyngeal type undifferentiated carcinoma", "shortest_name_length": 14}
{"curie": "MONDO:0019619", "names": ["duplication of the esophagus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "duplication of the esophagus", "shortest_name_length": 28}
{"curie": "MONDO:0007829", "names": ["ICP1", "pregnancy related cholestasis 1", "CHOLESTASIS, PREGNANCY-RELATED, 1", "cholestasis, pregnancy-related, 1", "intrahepatic cholestasis of pregnancy 1", "cholestasis, intrahepatic, of pregnancy, 1", "CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY, 1", "cholestasis, intrahepatic, of pregnancy, type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholestasis, intrahepatic, of pregnancy, 1", "shortest_name_length": 4}
{"curie": "MONDO:0020656", "names": ["HPV-related penile squamous cell carcinoma", "HPV-Related Penile Squamous Cell Carcinoma", "human papillomavirus-related penile squamous cell carcinoma", "Human Papillomavirus-Related Penile Squamous Cell Carcinoma", "Human Papilloma Virus-Related Penile Squamous Cell Carcinoma", "human papilloma virus-related penile squamous cell carcinoma", "human papilloma virus related penile squamous cell carcinoma", "Human Papilloma Virus Related Penile Squamous Cell Carcinoma", "Human Papillomavirus-Related Squamous Cell Carcinoma of the Penis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "human papillomavirus-related penile squamous cell carcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0020852", "names": ["SPGF31", "spermatogenic failure 31", "SPERMATOGENIC FAILURE 31"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 31", "shortest_name_length": 6}
{"curie": "UMLS:C4331244", "names": ["Resectable Head and Neck Squamous Cell Cancer", "Resectable Head and Neck Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Head and Neck Squamous Cell Carcinoma", "shortest_name_length": 45}
{"curie": "UMLS:C0023485", "names": ["Pre-B ALL", "Pro-B ALL", "Pre B-ALL", "Pre B ALL", "Pre-B-Cell Leukemia", "Pre B Cell Leukemia", "Leukemia, Pre B Cell", "Leukemia, Pre-B-Cell", "Pre-B-Cell Leukemias", "Leukemias, Pre-B-Cell", "Pre-B Acute Lymphoblastic Leukemia", "Precursor B Cell Lymphoblastic Lymphoma", "Precursor B-Cell Lymphoblastic Leukemia", "Precursor B-Cell Lymphoblastic Lymphoma", "Precursor B Cell Lymphoblastic Leukemia", "Precursor B-Cell Lymphoblastic Leukemia-Lymphoma", "Precursor B Cell Lymphoblastic Leukemia Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Precursor B-Cell Lymphoblastic Leukemia-Lymphoma", "shortest_name_length": 9}
{"curie": "UMLS:C0278660", "names": ["Synovial Sarcoma", "adult synovial sarcoma", "Adult Synovial Sarcoma", "synovial sarcoma, adult", "sarcoma, synovial, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Synovial Sarcoma", "shortest_name_length": 16}
{"curie": "MONDO:0008850", "names": ["Cooper Jabs syndrome", "Cooper-Jabs syndrome", "Aural Atresia, Multiple Congenital Anomalies, and Mental Retardation", "AURAL ATRESIA, MULTIPLE CONGENITAL ANOMALIES, AND MENTAL RETARDATION", "aural atresia, multiple congenital anomalies, and mental retardation", "aural atresia, multiple congenital anomalies, and intellectual disability", "aural atresia-multiple congenital anomalies-intellectual disability syndrome", "Aural atresia-multiple congenital anomalies-intellectual disability syndrome", "Aural atresia with multiple congenital anomalies and intellectual disability syndrome", "Aural atresia with multiple congenital anomalies and intellectual disability syndrome (disorder)", "Aural atresia with multiple congenital anomalies and intellectual disability syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cooper-Jabs syndrome", "shortest_name_length": 20}
{"curie": "MONDO:0019121", "names": ["pcp", "PJP", "PCP", "Pneumocystis", "PCP Pneumonia", "PCP Infection", "Pneumocystoses", "PCP Infections", "pneumocystosis", "Pneumonia, PCP", "PCP Pneumonias", "Infection, PCP", "Pneumocystosis", "Pneumonias, PCP", "P carinii Pneumonia", "P carinii Pneumonias", "Pneumonia, P carinii", "P. carinii Pneumonia", "Pneumonia, P. carinii", "P. carinii Pneumonias", "PNEUMOCYSTIS PNEUMONIA", "P. jirovecii Pneumonia", "pneumocystis pneumonia", "Pneumocystis Pneumonia", "Pneumocystis pneumonia", "Pneumonia, P. jirovecii", "PNEUMONIA, PNEUMOCYSTIS", "Pneumocystis Pneumonias", "P. jirovecii Pneumonias", "Pneumonia, Pneumocystis", "Pulmonary pneumocystosis", "Pneumocystosis pneumonia", "pneumocystosis pneumonia", "pulmonary pneumocystosis", "Pneumocystosis (disorder)", "Pneumocystosis, pulmonary", "PCP - Pneumocystis pneumonia", "Pneumocystis carinii Pneumonia", "pneumocystis carinii pneumonia", "Pneumocystis carinii pneumonia", "PNEUMOCYSTIS CARINII PNEUMONIA", "Pneumocystis Carinii Pneumonia", "Pneumonia, Pneumocystis carinii", "Pneumocystis jiroveci pneumonia", "PNEUMONIA, PNEUMOCYSTIS CARINII", "Pneumocystis jirovecii Pneumonia", "Pneumocystis jirovecii pneumonia", "Pneumonia, Pneumocystis jirovecii", "plasma cell interstitial pneumonia", "interstitial plasma cell pneumonia", "Pneumocystosis jirovecii pneumonia", "Interstitial plasma cell pneumonia", "PNEUMONIA, INTERSTITIAL PLASMA CELL", "Pneumonia, Interstitial Plasma Cell", "pneumocystis carinii pneumonia (PCP)", "PCP - Pneumocystis carinii pneumonia", "Pneumonia due to Pneumocystis carinii", "lymphoplasmacytic interstitial pneumonia", "Pneumocystis jiroveci pneumonia (diagnosis)", "Pneumocystosis jirovecii pneumonia (disorder)", "plasma cell interstitial pneumonia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pneumocystosis", "shortest_name_length": 3}
{"curie": "UMLS:C0751297", "names": ["Leptomeningeal Tumor", "Leptomeningeal disease", "Tumor of Leptomeninges", "LEPTOMENINGEAL DISEASE", "Leptomeningeal Neoplasm", "Leptomeningeal Neoplasms", "Neoplasm, Leptomeningeal", "Neoplasm of Leptomeninges", "Neoplasms, Leptomeningeal", "Tumor of the Leptomeninges", "Neoplasm of the Leptomeninges"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leptomeningeal Neoplasms", "shortest_name_length": 20}
{"curie": "UMLS:C1320835", "names": ["drug fever", "Drug Fever", "DRUG FEVER", "fever drug", "Drug fever", "drug fevers", "drugs fever", "Fever, Drug", "Drug Induced Fever", "Drug induced fever", "Drug-Induced Fever", "Drug-Induced Fevers", "Fever, Drug-Induced", "drug fever (diagnosis)", "Drug-Induced Hyperthermia", "Drug-induced hyperpyrexia", "Drug Induced Hyperthermia", "Drug-Induced Hyperthermias", "Hyperthermia, Drug-Induced", "Drug-induced hyperpyrexia (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drug Fever", "shortest_name_length": 10}
{"curie": "MONDO:0022529", "names": ["BKN", "PVAN", "BK virus nephropathy", "BK-virus nephropathy", "Polyomavirus nephropathy", "nephropathy from BK virus", "nephropathy due to BK polyomavirus", "Polyomavirus-associated nephropathy", "polyomavirus associated nephropathy", "nephropathy caused by BK polyomavirus", "Nephropathy caused by BK polyomavirus", "kidney disease caused by BK polyomavirus", "Kidney disease caused by BK polyomavirus", "nephropathy due to BK polyomavirus (diagnosis)", "Nephropathy caused by BK polyomavirus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "BK-virus nephropathy", "shortest_name_length": 3}
{"curie": "UMLS:C1336735", "names": ["t-AML", "Treatment related AML", "Treatment-Related AML", "Treatment Related AML", "Therapy-Related Acute Myeloid Leukemia", "Treatment related acute myeloid leukemia", "Treatment-related Acute Myeloid Leukemia", "Treatment Related Acute Myeloid Leukemia", "Treatment related acute myeloid leukaemia", "Treatment Related Acute Myelogenous Leukemia", "Treatment-Related Acute Myelogenous Leukemia", "High-Grade Treatment-Related Myeloid Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Treatment related acute myeloid leukaemia", "shortest_name_length": 5}
{"curie": "UMLS:C0239116", "names": ["Eye Burn", "burn cornea", "corneal burn", "cornea; burn", "Corneal burn", "CORNEAL BURN", "Corneal Burn", "burn; cornea", "burns cornea", "burns corneal", "burning cornea", "Burn of cornea", "burns of cornea", "Burn of cornea (disorder)", "burns of cornea (diagnosis)", "burns of cornea (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Corneal burn", "shortest_name_length": 8}
{"curie": "UMLS:C5420598", "names": ["Locally Advanced Rectal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Rectal Adenocarcinoma", "shortest_name_length": 38}
{"curie": "MONDO:0005258", "names": ["Kanner", "autism", "Autism", "AUTISM", "AUTISTIC", "autistic", "autistics", "Autism;child", "autism child", "child autism", "Kanner Syndrome", "atypical autism", "Autism disorder", "Autism (209850)", "childhood autism", "infantile autism", "Childhood autism", "Kanners Syndrome", "Autism infantile", "Infantile autism", "AUTISM INFANTILE", "autism infantile", "Infantile Autism", "autism childhood", "Autistic disorder", "Autism, Infantile", "Kanner's syndrome", "AUTISTIC DISORDER", "Autistic Disorder", "autistic disorder", "Kanner's Syndrome", "Disorder, Autistic", "autistic disorders", "autistic; disorder", "Autism in children", "disorder; autistic", "Disorders, Autistic", "Early infantile autism", "early infantile autism", "Autistic disorder, NOS", "Early Infantile Autism", "Autism, Early Infantile", "Autism, childhood onset", "Infantile Autism, Early", "autism spectrum disorder", "Autism Spectrum Disorder", "autistic spectrum disorder", "childhood autistic disorder", "Infantile autism (disorder)", "Autistic disorder (disorder)", "autistic disorder (diagnosis)", "Pervasive Developmental Disorders", "pervasive developmental disorders", "autistic disorder of childhood onset", "Autistic disorder of childhood onset", "infantile autistic disorder, full syndrome", "Autistic disorder of childhood onset (disorder)", "autistic disorder of childhood onset (diagnosis)", "infantile autistic disorder, full syndrome (diagnosis)", "pervasive developmental disorder - not otherwise specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autism spectrum disorder", "shortest_name_length": 6}
{"curie": "UMLS:C5420529", "names": ["Benign Inner Ear Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Inner Ear Neoplasm", "shortest_name_length": 25}
{"curie": "MONDO:0014825", "names": ["chromosome 11p13 deletion syndrome, distal", "CHROMOSOME 11p13 DELETION SYNDROME, DISTAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 11p13 deletion syndrome, distal", "shortest_name_length": 42}
{"curie": "MONDO:0005379", "names": ["neuroses", "Neuroses", "Neurosis", "neurosis", "NEUROSIS", "Neurosis NOS", "Neurosis, NOS", "PSYCHONEUROSIS", "psychoneurosis", "Psychoneurosis", "Psychoneuroses", "psychoneuroses", "neurosis; state", "neurotic; state", "state; neurotic", "state; neurosis", "Neurotic Disorder", "neurotic disorder", "Neurotic disorder", "neurotic; disorder", "Disorder, Neurotic", "Neurotic Disorders", "disorder, neurotic", "psychoneurosis NOS", "Psychoneurosis NOS", "neurotic disorders", "disorder; neurotic", "reactive depression", "Depression reactive", "Depression;reactive", "DEPRESSION REACTIVE", "neurotic depression", "Reactive depression", "REACTIVE DEPRESSION", "Depressive reaction", "Neurosis (disorder)", "disorders, neurotic", "Disorders, Neurotic", "depressive reaction", "Reactive Depression", "depressive neurosis", "reactive; depression", "Reactive Depressions", "depressive; reaction", "depression; reactive", "Depression, Reactive", "reaction; depressive", "neurosis (diagnosis)", "Depressions, Reactive", "Neurotic depressive state", "neurotic depressive state", "disorder; mental, neurotic", "mental; disorder, neurotic", "Nonpsychotic mental disorder", "Neurotic Depressive Reaction", "Unspecified neurotic disorder", "psychiatric disorders neurosis", "Neurotic disorder, unspecified", "Depressive Reaction (Neurotic)", "reactive depression (diagnosis)", "disease (or disorder); neurotic", "neurotic depression reactive type", "Reactive depression (situational)", "Nonpsychotic mental disorder, NOS", "Neurotic depression reactive type", "Reactive depression (situational) (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurotic disorder", "shortest_name_length": 8}
{"curie": "UMLS:C5420271", "names": ["Oropharyngeal Pleomorphic Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oropharyngeal Pleomorphic Adenoma", "shortest_name_length": 33}
{"curie": "MONDO:0033657", "names": ["HLD20", "hypomyelinating leukodystrophy 20", "leukodystrophy, hypomyelinating, 20", "LEUKODYSTROPHY, HYPOMYELINATING, 20"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukodystrophy, hypomyelinating, 20", "shortest_name_length": 5}
{"curie": "MONDO:0004923", "names": ["lacrimal passages; inflammation, chronic", "chronic inflammation of lacrimal passage", "Chronic inflammation of lacrimal passage", "inflammation; lacrimal passages, chronic", "inflammation of lacrimal passages chronic", "Chronic inflammation of lacrimal passages", "chronic inflammation of lacrimal passages", "Chronic inflammation of lacrimal drainage structure", "chronic inflammation of lacrimal passages (diagnosis)", "Chronic inflammation of lacrimal drainage structure (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic inflammation of lacrimal passage", "shortest_name_length": 40}
{"curie": "MONDO:0018943", "names": ["Zaspopathy (type)", "Desminopathy (type)", "Myofibrillar changes", "filaminopathy (type)", "myofibrillar myopathy", "Myofibrillar myopathy", "Myofibrillar Myopathy", "myotilinopathy (type)", "Myofibrillar Myopathies", "myofibrillar myopathies", "myofibrillar myopathy (disease)", "Myofibrillar myopathy (disorder)", "myofibrillar myopathy (diagnosis)", "Alpha Beta crystallinopathy (type)", "desmin related myopathy (former name)", "desmin storage myopathy (former name)", "Protein surplus myopathy (former name)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myofibrillar myopathy", "shortest_name_length": 17}
{"curie": "MONDO:0016356", "names": ["dSSc", "DcSSc", "dcSSc", "Diffuse Cutaneous Systemic Sclerosis", "diffuse cutaneous systemic sclerosis", "diffuse cutaneous systemic scleroderma", "progressive cutaneous systemic sclerosis", "progressive cutaneous systemic scleroderma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diffuse cutaneous systemic sclerosis", "shortest_name_length": 4}
{"curie": "MONDO:0015796", "names": ["ALI", "acute injury lung", "acute lung injury", "Acute lung injury", "Acute Lung Injury", "Lung Injury, Acute", "Acute Lung Injuries", "Lung Injuries, Acute", "ALI - Acute lung injury", "Acute lung injury (disorder)", "acute lung injury (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute lung injury", "shortest_name_length": 3}
{"curie": "MONDO:0001652", "names": ["Scrotal Melanoma", "scrotal melanoma", "scrotum melanoma", "scrotum; melanoma", "melanoma; scrotum", "Melanoma of Scrotum", "melanoma of scrotum", "Melanoma of the Scrotum", "melanoma of the scrotum", "scrotum melanoma (disease)", "melanoma (disease) of scrotum", "melanoma of scrotum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scrotum melanoma", "shortest_name_length": 16}
{"curie": "MONDO:0013373", "names": ["CMD1V", "dilated cardiomyopathy 1V", "Cardiomyopathy, Dilated, 1V", "cardiomyopathy, dilated, 1V", "CARDIOMYOPATHY, DILATED, 1V", "dilated cardiomyopathy type 1V", "cardiomyopathy, dilated, type 1V", "PSEN2 familial isolated dilated cardiomyopathy", "familial isolated dilated cardiomyopathy caused by mutation in PSEN2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1V", "shortest_name_length": 5}
{"curie": "MONDO:0012472", "names": ["AGS4", "Aicardi-Goutieres syndrome 4", "Aicardi-Goutieres Syndrome 4", "AICARDI-GOUTIERES SYNDROME 4", "Aicardi-Goutieres syndrome type 4", "RNASEH2A Aicardi-Goutieres syndrome", "RNASEH2A-related Aicardi-Goutieres syndrome", "Aicardi-Goutieres syndrome caused by mutation in RNASEH2A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aicardi-Goutieres syndrome 4", "shortest_name_length": 4}
{"curie": "UMLS:C5418792", "names": ["Advanced Oropharyngeal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Oropharyngeal Carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0013731", "names": ["EMARDD", "MEGF10 myopathy", "MEGF10-related myopathy", "congenital myopathy 10A", "congenital myopathy 10A, severe variant", "early-onset myopathy, areflexia, respiratory distress and dysphagia", "myopathy, areflexia, respiratory distress, and dysphagia, early-onset", "MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET", "Myopathy, areflexia, respiratory distress, and dysphagia, early-onset", "Early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome", "early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome", "Early-onset myopathy, areflexia, respiratory distress, dysphagia syndrome", "EMARDD (early-onset myopathy, areflexia, respiratory distress, dysphagia) syndrome", "MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET, MILD VARIANT", "myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant", "Early-onset myopathy, areflexia, respiratory distress, dysphagia syndrome (disorder)", "A congenital myopathy caused by mutations in the multiple epidermal growth factor-like domains 10 (MEGF10) gene, which causes early-onset myopathy characterized by severe weakness, scoliosis, joint contractures, areflexia, respiratory distress, and dysphagia, and a milder phenotype of minicore myopathy."], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MEGF10-related myopathy", "shortest_name_length": 6}
{"curie": "MONDO:0043183", "names": ["Podder-Tolmie syndrome", "podder-tolmie syndrome", "meningoencephalocele, arthrogryposis and hypoplastic thumbs", "Meningoencephalocele, arthrogryposis and hypoplastic thumbs"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "podder-tolmie syndrome", "shortest_name_length": 22}
{"curie": "UMLS:C1735324", "names": ["Fine Motor Delay", "Fine motor delay"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fine motor delay", "shortest_name_length": 16}
{"curie": "MONDO:0018145", "names": ["congenital retinal arteriovenous anastomoses", "congenital retinal arteriovenous communication", "congenital arteriovenous anastomoses of the retina", "congenital arteriovenous communication of the retina"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital retinal arteriovenous communication", "shortest_name_length": 44}
{"curie": "UMLS:C4683583", "names": ["Lugano Classification Stage IV Adult Non-Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage IV Adult Non-Hodgkin Lymphoma AJCC v8", "shortest_name_length": 65}
{"curie": "MONDO:0003237", "names": ["corpus uteri adenomyoma", "uterine body adenomyoma", "Uterine Body Adenomyoma", "Corpus Uteri Adenomyoma", "Uterine Corpus Adenomyoma", "body of uterus adenomyoma", "uterine corpus adenomyoma", "Adenomyoma of Corpus Uteri", "adenomyoma of Corpus Uteri", "adenomyoma of corpus uteri", "adenomyoma of uterine body", "Adenomyoma of Uterine Body", "Adenomyoma of Body of Uterus", "adenomyoma of uterine corpus", "Adenomyoma of Uterine Corpus", "adenomyoma of body of uterus", "Adenomyoma of the Corpus Uteri", "Adenomyoma of the Uterine Body", "adenomyoma of the uterine body", "adenomyoma of the corpus uteri", "Adenomyoma of the Uterine Corpus", "adenomyoma of the uterine corpus", "Adenomyoma of the Body of Uterus", "adenomyoma of the body of uterus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenomyoma of uterine corpus", "shortest_name_length": 23}
{"curie": "MONDO:0016225", "names": ["Specific Learning Disorder", "specific learning disorder", "Specific Learning Disorders", "Learning Disorder, Specific", "Disorder, Specific Learning", "specific learning difficulty", "specific learning disability", "Learning Disorders, Specific"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "specific learning disability", "shortest_name_length": 26}
{"curie": "MONDO:0043129", "names": ["Merlob Grunebaum Reisner syndrome", "merlob grunebaum reisner syndrome", "familial opposable triphalangeal thumbs associated with duplication of the big toes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "merlob grunebaum reisner syndrome", "shortest_name_length": 33}
{"curie": "MONDO:0015732", "names": ["Intermediate anorectal malformation", "intermediate anorectal malformation", "Intermediate anorectal malformation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intermediate anorectal malformation", "shortest_name_length": 35}
{"curie": "MONDO:0022932", "names": ["Davenport-Donlan syndrome", "Davenport Donlan syndrome", "dominant hearing loss, white hair, contractures, hyperkeratotic papillomata, and depressed chemotaxis", "Dominant hearing loss, white hair, contractures, hyperkeratotic papillomata, and depressed chemotaxis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Davenport-Donlan syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0009648", "names": ["Lisker Garcia Ramos syndrome", "Lisker-Garcia-Ramos syndrome", "Motor neuropathy peripheral with dysautonomia", "Hereditary dysautonomia with motor neuropathy", "motor neuropathy, peripheral, with dysautonomia", "Motor Neuropathy, Peripheral, with Dysautonomia", "MOTOR NEUROPATHY, PERIPHERAL, WITH DYSAUTONOMIA", "Peripheral motor neuropathy-dysautonomia syndrome", "peripheral motor neuropathy-dysautonomia syndrome", "Peripheral motor neuropathy dysautonomia syndrome", "Hereditary dysautonomia with motor neuropathy (disorder)", "Peripheral motor neuropathy associated with autonomic dysfunction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peripheral motor neuropathy-dysautonomia syndrome", "shortest_name_length": 28}
{"curie": "UMLS:C1704230", "names": ["Grade I Astrocytoma", "Grade I Astrocytomas", "Astrocytoma, Grade I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade I Astrocytoma", "shortest_name_length": 19}
{"curie": "MONDO:0019132", "names": ["spinal muscular atrophy-Dandy-Walker malformation-cataracts syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal muscular atrophy-Dandy-Walker malformation-cataracts syndrome", "shortest_name_length": 68}
{"curie": "UMLS:C1167750", "names": ["Hoigne's syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hoigne's syndrome", "shortest_name_length": 17}
{"curie": "UMLS:C4553575", "names": ["Stage III Renal Pelvis Cancer", "Stage III Renal Pelvis Cancer AJCC v8", "Stage III Renal Pelvis Urothelial Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Renal Pelvis Cancer AJCC v8", "shortest_name_length": 29}
{"curie": "MONDO:0011389", "names": ["DFNA16", "autosomal dominant deafness 16", "DEAFNESS, AUTOSOMAL DOMINANT 16", "deafness, autosomal dominant 16", "Deafness, Autosomal Dominant 16", "autosomal dominant nonsyndromic deafness 16", "autosomal dominant nonsyndromic hearing loss 16", "autosomal dominant nonsyndromic deafness type 16"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 16", "shortest_name_length": 6}
{"curie": "MONDO:0000137", "names": ["leukoencephalopathy, megalencephalic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukoencephalopathy, megalencephalic", "shortest_name_length": 36}
{"curie": "UMLS:C4331324", "names": ["Stage II Nasopharyngeal Throat Cancer", "Stage II Nasopharyngeal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Nasopharyngeal Carcinoma AJCC v8", "shortest_name_length": 37}
{"curie": "UMLS:C4520721", "names": ["Relapsed Skin T-Cell Lymphoma", "Recurrent Skin T-Cell Lymphoma", "Relapsed T-Cell Lymphoma of Skin", "Recurrent T-Cell Lymphoma of Skin", "Relapsed Cutaneous T-Cell Lymphoma", "Relapsed T-Cell Lymphoma of the Skin", "Recurrent T-Cell Lymphoma of the Skin", "Recurrent Cutaneous T-Cell Non-Hodgkin Lymphoma", "Recurrent Cutaneous T-Cell Non-Hodgkin's Lymphoma", "Recurrent Primary Cutaneous T-Cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Primary Cutaneous T-Cell Non-Hodgkin Lymphoma", "shortest_name_length": 29}
{"curie": "UMLS:C0334642", "names": ["Malignant lymphoma, noncleaved, NOS", "Malignant Lymphoma, Non-Cleaved, Diffuse", "Malignant lymphoma, noncleaved, diffuse, NOS", "Malignant lymphoma, large cell, noncleaved, NOS", "Diffuse malignant lymphoma - large non-cleaved cell", "diffuse malignant lymphoma - large non cleaved cell", "Malignant lymphoma, large cell, noncleaved, diffuse", "Diffuse malignant lymphoma - large non-cleaved cell (disorder)", "diffuse malignant lymphoma - large non cleaved cell (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse malignant lymphoma - large non-cleaved cell", "shortest_name_length": 35}
{"curie": "UMLS:C0158644", "names": ["lung; anomaly", "anomaly; lung", "deformity; lung", "lung; deformity", "pulmonary anomaly", "pulmonary; anomaly", "anomaly; pulmonary", "PULMONARY ANOMALY NOS", "congenital anomaly of lung", "Congenital anomaly of lung", "anomaly; lungs, congenital", "Congenital lung malformation", "congenital lung malformation", "Congenital Lung Malformation", "Anomaly of lung, unspecified", "Congenital Abnormality of Lung", "Congenital malformation of lung", "Congenital anomaly of lung, NOS", "Congenital lung malformation NOS", "CONGENITAL ANOMALIES OF THE LUNG", "Congenital malformations of lung", "Congenital lung malformation, NOS", "Congenital anomaly of lung (disorder)", "congenital anomaly of lung (diagnosis)", "Congenital anomaly of lung, unspecified", "Congenital malformation of lung, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital anomaly of lung", "shortest_name_length": 13}
{"curie": "MONDO:0015165", "names": ["AML and myelodysplastic syndromes related to topoisomerase type 2 inhibitor", "acute myeloid leukemia and myelodysplastic syndromes related to topoisomerase type 2 inhibitor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia and myelodysplastic syndromes related to topoisomerase type 2 inhibitor", "shortest_name_length": 75}
{"curie": "UMLS:C5557316", "names": ["DS Stage IIIA Plasma Cell Myeloma", "Durie/Salmon Stage IIIA Plasma Cell Myeloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DS Stage IIIA Plasma Cell Myeloma", "shortest_name_length": 33}
{"curie": "MONDO:0029142", "names": ["DFNB111", "autosomal recessive deafness 111", "DEAFNESS, AUTOSOMAL RECESSIVE 111", "deafness, autosomal recessive 111", "hearing loss, autosomal recessive 111", "autosomal recessive nonsyndromic deafness 111"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal recessive 111", "shortest_name_length": 7}
{"curie": "UMLS:C5556718", "names": ["Advanced Bronchogenic Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Bronchogenic Carcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C0745390", "names": ["Intrauterine Mass", "INTRAUTERINE MASS", "Uterine Body Mass", "Uterine Corpus Mass", "Mass of Uterine Body", "Mass of Uterine Corpus", "Mass of the Uterine Body", "Mass of the Uterine Corpus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intrauterine Mass", "shortest_name_length": 17}
{"curie": "MONDO:0100450", "names": ["VRNI", "ADNIV", "Retinitis proliferans", "retinitis proliferans", "CAPN5 vitreoretinopathy", "proliferative vitreoretinopathy", "CAPN5-related vitreoretinopathy", "neovascular inflammatory vitreoretinopathy", "vitreoretinopathy, neovascular inflammatory", "autosomal dominant neovascular inflammatory vitreoretinopathy", "Autosomal dominant neovascular inflammatory vitreoretinopathy", "VITREORETINOPATHY, NEOVASCULAR INFLAMMATORY, AUTOSOMAL DOMINANT", "vitreoretinopathy, neovascular inflammatory, autosomal dominant", "Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CAPN5-related vitreoretinopathy", "shortest_name_length": 4}
{"curie": "MONDO:0008602", "names": ["triglyceride storage disease, type 2", "Triglyceride Storage Disease, Type II", "TRIGLYCERIDE STORAGE DISEASE, TYPE II", "triglyceride storage disease, type II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "triglyceride storage disease, type 2", "shortest_name_length": 36}
{"curie": "UMLS:C0338762", "names": ["continuous cocaine dependence", "COCAINE DEPENDENCY CONTINUOUS", "Cocaine dependence, continuous", "Cocaine dependence, continuous use", "Cocaine Dependence, Continuous Use", "Cocaine dependence, continuous (disorder)", "continuous cocaine dependence (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cocaine dependence, continuous", "shortest_name_length": 29}
{"curie": "UMLS:C5206568", "names": ["Intermediate Risk Acute Myeloid Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intermediate Risk Acute Myeloid Leukemia", "shortest_name_length": 40}
{"curie": "MONDO:0020455", "names": ["congenital partial agenesis of pericardium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital partial agenesis of pericardium", "shortest_name_length": 42}
{"curie": "MONDO:0000708", "names": ["jejunoileitis", "Crohn jejunoileitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Crohn jejunoileitis", "shortest_name_length": 13}
{"curie": "UMLS:C3888672", "names": ["Infusion site discharge"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infusion site discharge", "shortest_name_length": 23}
{"curie": "UMLS:C0346975", "names": ["Metastases to rectum", "Metastasis to the Rectum", "metastatic rectal cancer", "rectal cancer metastatic", "Cancer metastatic to rectum", "Metastatic Tumor to the Rectum", "Metastatic Neoplasm to the Rectum", "rectal malignant neoplasm secondary", "Secondary malignant neoplasm of rectum", "secondary malignant neoplasm of rectum", "Metastatic malignant neoplasm of rectum", "Metastatic malignant neoplasm to rectum", "Metastatic Malignant Neoplasm in the Rectum", "Metastatic Malignant Neoplasm to the Rectum", "Metastatic malignant neoplasm to rectum (disorder)", "secondary malignant neoplasm of rectum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary malignant neoplasm of rectum", "shortest_name_length": 20}
{"curie": "MONDO:0013848", "names": ["CMD2B", "dilated cardiomyopathy 2B", "cardiomyopathy, dilated, 2B", "CARDIOMYOPATHY, DILATED, 2B", "dilated cardiomyopathy type 2B", "cardiomyopathy, dilated, type 2B", "GATAD1 familial isolated dilated cardiomyopathy", "familial isolated dilated cardiomyopathy caused by mutation in GATAD1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 2B", "shortest_name_length": 5}
{"curie": "UMLS:C0862196", "names": ["Mycosis fungoides/Sezary syndrome", "mycosis fungoides/Sezary syndrome", "fungoides mycosis sezary syndrome", "mycosis fungoides/sezary syndrome nos", "Mycosis Fungoides and Sézary Syndrome", "Mycosis fungoides/Sezary syndrome NOS", "Mycosis Fungoides and Sezary Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mycosis fungoides/Sezary syndrome", "shortest_name_length": 33}
{"curie": "UMLS:C0154583", "names": ["Prolonged depressive reaction", "Prolonged depressive adjustment reaction", "Prolonged depressive adjustment reaction (disorder)", "Adjustment reaction with prolonged depressive reaction", "Adjustment Reaction with Prolonged Depressive Reaction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prolonged depressive adjustment reaction", "shortest_name_length": 29}
{"curie": "MONDO:0021193", "names": ["neuroepithelial tumor", "Neuroepithelial Tumor", "Tumor, Neuroepithelial", "neuroepithelial tumors", "Neuroepithelial Tumors", "Tumors, Neuroepithelial", "Tumor of Neuroepithelium", "Neuroepithelial Neoplasm", "tumor of neuroepithelium", "Neuroepithelial neoplasm", "neuroepithelial neoplasm", "neuroepithelial neoplasms", "Neuroepithelial Neoplasms", "Neoplasm, Neuroepithelial", "Neoplasms, Neuroepithelial", "neoplasm of neuroepithelium", "Neoplasm of Neuroepithelium", "neuroepithelial tissue tumor", "Neuroepithelial Tissue Tumor", "Tumor of the Neuroepithelium", "tumor of the neuroepithelium", "Neuroepitheliomatous neoplasm", "primary neuroepithelial tumor", "Neuroepitheliomatous Neoplasms", "NEUROEPITHELIOMATOUS NEOPLASMS", "Tumor of Neuroepithelial Tissue", "Neoplasm of the Neuroepithelium", "tumor of neuroepithelial tissue", "Neuroepithelial Tissue Neoplasm", "neoplasm of the neuroepithelium", "neuroepithelial tissue neoplasm", "neoplasm of neuroepithelial tissue", "Neoplasm of Neuroepithelial Tissue", "Neuroepitheliomatous neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuroepithelial neoplasm", "shortest_name_length": 21}
{"curie": "MONDO:0003490", "names": ["Ampulla of Vater Squamous Cell Carcinoma", "ampulla of Vater squamous cell carcinoma", "ampulla of vater squamous cell carcinoma", "hepatopancreatic ampulla squamous cell carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ampulla of vater squamous cell carcinoma", "shortest_name_length": 40}
{"curie": "UMLS:C3854457", "names": ["Foreign body embolism", "Foreign Body Embolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Foreign body embolism", "shortest_name_length": 21}
{"curie": "UMLS:C0010074", "names": ["Coronary Vessel Anomaly", "Anomaly, Coronary Vessel", "Coronary Vessel Anomalies", "anomaly; coronary artery or vein", "Malformation of coronary vessels", "malformations of coronary vessels", "coronary artery or vein; artery, anomaly", "malformations of coronary vessels (diagnosis)", "congenital heart defect malformations coronary vessels"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Coronary Vessel Anomalies", "shortest_name_length": 23}
{"curie": "MONDO:0032913", "names": ["CHTD7", "congenital heart defects, multiple types, 7", "CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital heart defects, multiple types, 7", "shortest_name_length": 5}
{"curie": "MONDO:0030967", "names": ["DEAPLE", "deafness, congenital, and adult-onset progressive leukoencephalopathy", "DEAFNESS, CONGENITAL, AND ADULT-ONSET PROGRESSIVE LEUKOENCEPHALOPATHY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness, congenital, and adult-onset progressive leukoencephalopathy", "shortest_name_length": 6}
{"curie": "UMLS:C0334386", "names": ["Breast Paget Disease with Invasive Ductal Carcinoma", "Paget's disease and invasive ductal carcinoma of breast", "Paget disease and infiltrating duct carcinoma of breast", "Paget's Disease and Invasive Ductal Carcinoma of Breast", "Paget's disease of breast with invasive ductal carcinoma", "Paget's Disease of Breast with Invasive Ductal Carcinoma", "Paget's disease and infiltrating duct carcinoma of breast", "Paget Disease of the Breast with Invasive Ductal Carcinoma", "Paget disease of the breast with invasive ductal carcinoma", "Paget's disease and invasive ductal carcinoma of the breast", "Paget's Disease and Invasive Ductal Carcinoma of the Breast", "Paget's disease and infiltrating ductal carcinoma of breast", "Paget's Disease and Infiltrating Ductal Carcinoma of Breast", "Paget's disease of the breast with invasive ductal carcinoma", "Paget's Disease of Breast with Infiltrating Ductal Carcinoma", "Paget's Disease of the Breast with Invasive Ductal Carcinoma", "Paget's disease of breast with infiltrating ductal carcinoma", "Paget's Disease and Infiltrating Ductal Carcinoma of the Breast", "Paget's disease and infiltrating ductal carcinoma of the breast", "Paget's disease of the breast with infiltrating ductal carcinoma", "Paget's Disease of the Breast with Infiltrating Ductal Carcinoma", "Paget's disease and infiltrating duct carcinoma of breast (diagnosis)", "Paget's disease and infiltrating duct carcinoma of breast (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paget's disease and infiltrating duct carcinoma of breast", "shortest_name_length": 51}
{"curie": "MONDO:0000482", "names": ["graphospasm", "Graphospasm", "Writers' cramp", "Writers' spasm", "writer's cramp", "Writer's cramp", "writer; cramp(s)", "cramp(s); writer", "Scriveners' palsy", "Writers' paralysis", "focal hand dystonia", "organic; graphospasm", "graphospasm; organic", "Paralysis notariorum", "hand and arm dystonia", "organic writer's cramp", "Organic writers' cramp", "Organic writer's cramp", "cramp(s); writer, organic", "writer; cramp(s), organic", "Organic writer's cramp (disorder)", "organic writer's cramp (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal hand dystonia", "shortest_name_length": 11}
{"curie": "UMLS:C5555528", "names": ["Refractory Acute Bilineal Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Acute Bilineal Leukemia", "shortest_name_length": 34}
{"curie": "MONDO:0006403", "names": ["pleomorphic adenoma carcinoma", "carcinoma ex pleomorphic adenoma", "carcinoma in pleomorphic adenoma", "salivary gland carcinoma ex pleomorphic adenoma", "Salivary Gland Carcinoma ex Pleomorphic Adenoma", "carcinoma ex pleomorphic adenoma of salivary gland", "saliva-secreting gland carcinoma ex pleomorphic adenoma", "carcinoma ex pleomorphic adenoma of salivary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "salivary gland carcinoma ex pleomorphic adenoma", "shortest_name_length": 29}
{"curie": "MONDO:0018762", "names": ["congenital hypopituitarism", "congenital combined pituitary hormone deficiency", "non-acquired combined pituitary hormone deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-acquired combined pituitary hormone deficiency", "shortest_name_length": 26}
{"curie": "MONDO:0007670", "names": ["hypotrichosis lymphedema telangiectasia syndrome", "hypotrichosis-lymphedema-telangiectasia syndrome (grouping)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotrichosis-lymphedema-telangiectasia syndrome (grouping)", "shortest_name_length": 48}
{"curie": "MONDO:0001249", "names": ["Trachoma", "trachoma", "TRACHOMA", "Trachomas", "Trachoma NOS", "Trachoma, NOS", "active trachoma", "Trachoma dubium", "trachoma dubium", "trachoma; active", "dubium; trachoma", "trachoma; dubium", "active; trachoma", "trachoma; initial", "initial; trachoma", "Trachoma (disorder)", "Egyptian Ophthalmia", "trachoma (diagnosis)", "Ophthalmia, Egyptian", "active stage trachoma", "Trachoma, unspecified", "trachomatis; Chlamydia", "initial stage trachoma", "Trachoma, active stage", "Trachoma, initial stage", "Trachoma - active stage", "Active stage of trachoma", "Initial stage of trachoma", "active trachoma (diagnosis)", "Trachoma dubium - initial stage", "Trachoma, active stage (disorder)", "initial stage trachoma (diagnosis)", "Trachoma, initial stage (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trachoma", "shortest_name_length": 8}
{"curie": "UMLS:C1699655", "names": ["Ileal Fistula", "Ileal fistula", "ileum; fistula", "fistula; ileum", "small bowel fistula ileum", "Ileal fistula (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ileal Fistula", "shortest_name_length": 13}
{"curie": "MONDO:0002720", "names": ["selt", "SELLAR TUMOR", "sellar tumor", "Sellar Tumor", "Sellar Neoplasm", "sellar neoplasm", "Sella Turcica Tumor", "sella turcica tumor", "tumor of Sella Turcica", "Sella Turcica Neoplasm", "Sellar Region Neoplasm", "sella turcica neoplasm", "tumor of sella turcica", "neoplasm of sella turcica", "Neoplasm of Sella Turcica", "tumor of the sella turcica", "Tumor of the Sellar Region", "Tumor of the Sella Turcica", "neoplasm in the sella turcica", "Neoplasm of the Sella Turcica", "Neoplasm of the Sellar Region", "neoplasm of the sella turcica", "location of neoplasm of sella turcica", "location of neoplasm of sella turcica (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sella turcica neoplasm", "shortest_name_length": 4}
{"curie": "MONDO:0044699", "names": ["SIN3A-related intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SIN3A-related intellectual disability syndrome", "shortest_name_length": 46}
{"curie": "UMLS:C0041909", "names": ["bleed ugi", "ugi bleed", "UGI bleed", "bleeds ugi", "bleeding ugi", "bleed gi upper", "upper gi bleed", "bleeds gi upper", "Upper GI bleeding", "upper gi bleeding", "upper GI bleeding", "bleeding gi upper", "upper gi hemorrhage", "Upper GI hemorrhage", "Upper GI blood loss", "gi haemorrhage upper", "upper gi haemorrhage", "Upper GI haemorrhage", "upper gastrointestinal bleed", "GASTROINTESTINAL BLEED UPPER", "bleed gastrointestinal upper", "upper gastrointestinal bleeding", "UPPER GASTROINTESTINAL BLEEDING", "Upper gastrointestinal bleeding", "bleeding gastrointestinal upper", "Upper Gastrointestinal Hemorrhage", "Upper gastrointestinal hemorrhage", "Upper gastrointestinal haemorrhage", "Upper GI - gastrointestinal hemorrhage", "Upper GI - gastrointestinal haemorrhage", "upper gastrointestinal bleeding (diagnosis)", "Upper gastrointestinal hemorrhage (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Upper gastrointestinal hemorrhage", "shortest_name_length": 9}
{"curie": "MONDO:0018352", "names": ["PSCC", "PENIS CANCER SQUAMOUS CELL", "penile epidermoid carcinoma", "penile squamous cell cancer", "Penile Epidermoid Carcinoma", "Penile Squamous Cell Cancer", "epidermoid carcinoma, penile", "PENIS, CARCINOMA, EPIDERMOID", "epidermoid carcinoma of penis", "Epidermoid Carcinoma of Penis", "penis squamous cell carcinoma", "carcinoma cell penis squamous", "penile squamous cell carcinoma", "squamous cell carcinoma penile", "Penile squamous cell carcinoma", "Penile Squamous Cell Carcinoma", "squamous cell carcinoma, penile", "PENIS, CARCINOMA, SQUAMOUS CELL", "carcinoma cell of penis squamous", "penile squamous car.(epidermoid)", "penile epidermoid cell carcinoma", "Squamous Cell Carcinoma of Penis", "Squamous cell carcinoma of penis", "Penile Epidermoid Cell Carcinoma", "Penile squamous car.(epidermoid)", "squamous cell carcinoma of penis", "Epidermoid Carcinoma of the Penis", "epidermoid carcinoma of the penis", "penis cancer, epidermoid carcinoma", "epidermoid cell carcinoma of penis", "Epidermoid cell carcinoma of penis", "Epidermoid Cell Carcinoma of Penis", "Cancer of the penis, squamous cell", "penile cancer, epidermoid carcinoma", "squamous cell carcinoma of the penis", "PENILE CANCER, CARCINOMA, EPIDERMOID", "Squamous cell carcinoma of the penis", "Squamous Cell Carcinoma of the Penis", "penis cancer, squamous cell carcinoma", "Epidermoid Cell Carcinoma of the Penis", "penile cancer, squamous cell carcinoma", "epidermoid cell carcinoma of the penis", "Penile squamous carcinoma (epidermoid)", "penile squamous carcinoma (epidermoid)", "Penile Squamous Cell Carcinoma, Usual Type", "Squamous cell carcinoma of penis (disorder)", "Squamous Cell Carcinoma of Penis, Usual Type", "squamous cell carcinoma of penis (diagnosis)", "Squamous Cell Carcinoma of the Penis, Usual Type", "Squamous cell Carcinoma of the Penis, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "squamous cell carcinoma of penis", "shortest_name_length": 4}
{"curie": "UMLS:C4520774", "names": ["Stage IVB Vulvar Cancer", "Stage IVB Vulval Cancer", "Stage IVB Vulva Carcinoma", "Stage IVB Vulval Carcinoma", "Stage IVB Vulvar Carcinoma", "Stage IVB Carcinoma of Vulva", "Stage IVB Vulvar Cancer AJCC v7", "Stage IVB Vulvar Cancer AJCC v6", "Stage IVB Carcinoma of the Vulva", "Stage IVB Vulvar Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Vulvar Cancer AJCC v6 and v7", "shortest_name_length": 23}
{"curie": "MONDO:0012696", "names": ["OTSC4", "Otosclerosis 4", "otosclerosis 4", "OTOSCLEROSIS 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "otosclerosis 4", "shortest_name_length": 5}
{"curie": "UMLS:C3888639", "names": ["Application site extravasation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Application site extravasation", "shortest_name_length": 30}
{"curie": "UMLS:C0278694", "names": ["Stage 4 Neuroblastoma", "stage 4 neuroblastoma", "Stage IV Neuroblastoma", "stage iv neuroblastoma", "Metastatic neuroblastoma", "metastatic neuroblastoma", "Disseminated neuroblastoma", "Disseminated Neuroblastoma", "Metastatic neuroblastoma (disorder)", "Metastatic neuroblastoma (diagnosis)", "malignant neoplasm neuroblastoma metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disseminated neuroblastoma", "shortest_name_length": 21}
{"curie": "MONDO:0001799", "names": ["localised anterior staphyloma", "Anterior localised staphyloma", "Localized anterior staphyloma", "Anterior localized staphyloma", "localized anterior staphyloma", "Localised anterior staphyloma", "Anterior staphyloma, localized", "anterior staphyloma, localized", "Anterior staphyloma, localised", "Localized anterior staphyloma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "localized anterior staphyloma", "shortest_name_length": 29}
{"curie": "MONDO:0019010", "names": ["chi", "PHHI", "HHF1", "congenital hyperinsulinism", "hyperinsulinism congenital", "congenital isolated hyperinsulinism", "hyperinsulinemic hypoglycemia familial", "hypoglycemia hyperinsulinemic of infancy", "Familial Hyperinsulinemic Hypoglycemia-1", "persistent hyperinsulinemic hypoglycemia of infancy", "Persistent Hyperinsulinemic Hypoglycemia of Infancy", "hyperinsulinism familial with pancreatic nesidioblastosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital isolated hyperinsulinism", "shortest_name_length": 3}
{"curie": "MONDO:0014756", "names": ["ETM5", "essential tremor 5", "TENM4 essential tremor", "hereditary essential tremor 5", "essential tremor, hereditary, 5", "tremor, hereditary essential, 5", "TREMOR, HEREDITARY ESSENTIAL, 5", "tremor, hereditary essential, type 5", "tremor, hereditary essential, 5; ETM5", "essential tremor caused by mutation in TENM4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tremor, hereditary essential, 5", "shortest_name_length": 4}
{"curie": "MONDO:0012127", "names": ["LGMD2J", "LGMDR10", "LGMD type 2J", "Titin-related LGMD R10", "limb-girdle muscular dystrophy type 2J", "Limb-girdle muscular dystrophy type 2J", "Muscular Dystrophy, Limb-Girdle, Type 2J", "muscular dystrophy, limb-girdle, type 2J", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2J", "Titin-related limb-girdle muscular dystrophy R10", "Limb-girdle muscular dystrophy 2J titin gene mutation", "TTN autosomal recessive limb-girdle muscular dystrophy", "muscular dystrophy, limb-girdle, autosomal recessive 10", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 10", "autosomal recessive limb-girdle muscular dystrophy type 2J", "Autosomal recessive limb girdle muscular dystrophy type 2J", "Autosomal recessive limb-girdle muscular dystrophy type 2J", "Autosomal recessive limb girdle muscular dystrophy type 2J (disorder)", "autosomal recessive limb-girdle muscular dystrophy caused by mutation in TTN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive limb-girdle muscular dystrophy type 2J", "shortest_name_length": 6}
{"curie": "UMLS:C0751859", "names": ["Neurologic Plumbism", "Plumbism, Neurologic", "Nervous System Plumbism", "Plumbism, Nervous System", "Neurologic Lead Poisoning", "Lead Poisoning, Neurologic", "Lead Neurotoxicity Syndrome", "Poisoning, Lead, Neurologic", "Syndrome, Lead Neurotoxicity", "Neurotoxicity Syndrome, Lead", "Lead Neurotoxicity Syndromes", "Syndromes, Lead Neurotoxicity", "Neurotoxicity Syndromes, Lead", "Lead Poisoning, Nervous System", "Nervous System Poisoning, Lead", "Poisoning, Lead, Nervous System", "Lead-Induced Nervous System Diseases", "Nervous System Diseases, Lead-Induced"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lead Poisoning, Nervous System", "shortest_name_length": 19}
{"curie": "MONDO:0015898", "names": ["Wilkins disease", "adrenal virilism", "Adrenal virilism", "Androgenital syndrome", "androgenital syndrome", "Adrenogenital syndrome", "adrenogenital disorder", "Adrenogenital Syndrome", "Apert-Gallais syndrome", "adrenogenital syndrome", "ADRENOGENITAL SYNDROME", "syndrome; adrenogenital", "Adrenogenital Syndromes", "adrenogenital; syndrome", "Syndrome, Adrenogenital", "Syndromes, Adrenogenital", "Adrenal virilism syndrome", "Adrenogenital syndrome NOS", "Adrenal virilism (disorder)", "adrenal virilization syndrome", "congenital adrenal hyperplasia", "Congenital adrenogenital syndrome", "Adrenogenital syndrome congenital", "ADRENOGENITAL SYNDROME CONGENITAL", "ADRENOGENITAL SYNDROME, CONGENITAL", "Adrenogenital syndrome, congenital", "congenital; adrenogenital syndrome", "adrenogenital; syndrome, congenital", "Congenital adrenal cortical hyperplasia", "adrenal virilization syndrome (diagnosis)", "Congenital adrenal cortical hyperplasia, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adrenogenital syndrome", "shortest_name_length": 15}
{"curie": "UMLS:C1881406", "names": ["Lipase Hypersecretion Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lipase Hypersecretion Syndrome", "shortest_name_length": 30}
{"curie": "UMLS:C1334671", "names": ["Mediastinal Mixed Non-Seminomatous Germ Cell Tumor", "Mediastinal Mixed Nongerminomatous Germ Cell Tumor", "Mediastinal Mixed Non-Seminomatous Germ Cell Neoplasm", "Mixed Non-Seminomatous Germ Cell Tumor of Mediastinum", "Mixed Non-Seminomatous Germ Cell Neoplasm of Mediastinum", "Mixed Non-Seminomatous Germ Cell Tumor of the Mediastinum", "Mixed Non-Seminomatous Germ Cell Neoplasm of the Mediastinum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mediastinal Mixed Nongerminomatous Germ Cell Tumor", "shortest_name_length": 50}
{"curie": "EFO:1001489", "names": ["skin and soft tissue Staphylococcus aureus infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin and soft tissue Staphylococcus aureus infection", "shortest_name_length": 52}
{"curie": "MONDO:0018485", "names": ["GSD type 2, late-onset", "GSD type 2, late onset", "GSD type II, late-onset", "GSD type II, late onset", "Pompe disease, late-onset", "Pompe disease, late onset", "Pompe's disease late onset", "Pompe's disease adult onset", "glycogenosis type 2, late onset", "Glycogenosis type 2, late-onset", "glycogenosis type 2, late-onset", "glycogenosis type II, late onset", "Glycogenosis type II, late-onset", "glycogenosis type II, late-onset", "Glycogenosis type II, late onset", "glycogen storage disease type 2, late-onset", "glycogen storage disease type 2, late onset", "Glycogen storage disease type II late onset", "Glycogen storage disease type 2, late-onset", "glycogen storage disease type II, late-onset", "Glycogen storage disease type II, late-onset", "glycogen storage disease type II, late onset", "GSD due to acid maltase deficiency, late onset", "GSD due to acid maltase deficiency, late-onset", "Alpha-1,4-glucosidase acid deficiency, late onset", "Alpha-1,4-glucosidase acid deficiency, late-onset", "Glycogen storage disease type II late onset (disorder)", "Lysosomal alpha-1,4-glucosidase deficiency - adult onset", "glycogen storage disease due to acid maltase deficiency, late-onset", "Glycogen storage disease due to acid maltase deficiency, late-onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease due to acid maltase deficiency, late-onset", "shortest_name_length": 22}
{"curie": "UMLS:C0600176", "names": ["Argentaffinoma", "argentaffinoma", "Argentaffinomas", "Argentaffinoma, NOS", "Carcinoid tumor, argentaffin", "Carcinoid tumor - argentaffin", "Carcinoid tumour - argentaffin", "Carcinoid tumor, argentaffin NOS", "Carcinoid tumour, argentaffin NOS", "Carcinoid tumor, argentaffin, NOS", "Carcinoid tumour, argentaffin, NOS", "[M]Carcinoid tumor, argentaffin, NOS", "[M]Carcinoid tumour, argentaffin, NOS", "Carcinoid Tumor of Uncertain Malignant Potential", "Carcinoid tumor of uncertain malignant potential", "Carcinoid tumor - argentaffin (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Argentaffinoma", "shortest_name_length": 14}
{"curie": "MONDO:0022180", "names": ["trisomy 16", "mosaic trisomy 16", "chromosome 16 trisomy", "trisomy chromosome 16"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 16 trisomy", "shortest_name_length": 10}
{"curie": "MONDO:0021578", "names": ["sternal tumor", "sternum tumor", "Sternal Tumor", "sternal neoplasm", "sternum neoplasm", "tumor of sternum", "Tumor of Sternum", "Sternal Neoplasm", "neoplasm of sternum", "Neoplasm of Sternum", "Neoplasm of sternum", "Tumor of the Sternum", "tumor of the sternum", "neoplasm of the sternum", "bone neoplasm - sternum", "Neoplasm of the Sternum", "sternum neoplasm (disease)", "neoplasm of sternum (disease)", "neoplasm of sternum (disorder)", "Neoplasm of sternum (disorder)", "Neoplasm of sternum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sternal neoplasm", "shortest_name_length": 13}
{"curie": "UMLS:C3146268", "names": ["Stage I Esophageal Cancer", "Stage I Esophageal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Esophageal Cancer AJCC v7", "shortest_name_length": 25}
{"curie": "UMLS:C0278851", "names": ["Stage IV Papillary Thyroid Cancer", "stage IV papillary thyroid cancer", "thyroid cancer, stage IV papillary", "papillary thyroid cancer, stage IV", "metastatic papillary thyroid cancer", "Stage IV Thyroid Papillary Carcinoma", "papillary thyroid cancer, metastatic", "thyroid cancer, metastatic papillary", "Metastatic papillary thyroid carcinoma", "Stage IV Papillary Carcinoma of Thyroid", "Stage IV Thyroid Gland Papillary Cancer", "Stage IV Thyroid Gland Papillary Carcinoma", "Stage IV Papillary Thyroid Gland Carcinoma", "Stage IV Papillary Carcinoma of the Thyroid", "adenocarcinoma, papillary, thyroid, stage IV", "mixed adenocarcinoma of the thyroid, stage IV", "Stage IV Papillary Carcinoma of Thyroid Gland", "adenocarcinoma, papillary, thyroid, metastatic", "mixed adenocarcinoma of the thyroid, metastatic", "Stage IV Papillary Carcinoma of the Thyroid Gland", "papillary adenocarcinoma of the thyroid, stage IV", "Stage IV Thyroid Gland Papillary Carcinoma AJCC v7", "papillary adenocarcinoma of the thyroid, metastatic", "Metastatic papillary thyroid carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Thyroid Gland Papillary Carcinoma AJCC v7", "shortest_name_length": 33}
{"curie": "MONDO:0016144", "names": ["delta-sarcoglycanopathy", "qualitative or quantitative defects of delta-sarcoglycan"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of delta-sarcoglycan", "shortest_name_length": 23}
{"curie": "UMLS:C0391861", "names": ["Plasmacytic Infiltrate", "Plasmacytic infiltrate", "Plasma cell inflammation", "Plasma cell infiltration", "Plasmacytic infiltrate, NOS", "Plasma cell infiltration, NOS", "Plasma cell inflammation, NOS", "Plasma cell inflammation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Plasma cell inflammation", "shortest_name_length": 22}
{"curie": "MONDO:0035941", "names": ["B-lymphoblastic leukemia/lymphoma with t(v;11q23.3)", "B lymphoblastic leukemia/lymphoma with t(v;11q23); MLL rearranged", "B lymphoblastic leukemia lymphoma with t(v;11q23); MLL rearranged", "B-Lymphoblastic Leukemia/Lymphoma with t(v;11q23); MLL Rearranged", "B lymphoblastic leukaemia lymphoma with t(v;11q23); MLL rearranged", "B Lymphoblastic Leukemia/Lymphoma with t(v;11q23.3); MLL Rearranged", "B Lymphoblastic Leukemia/Lymphoma with t(v;11q23.3); KMT2A Rearranged", "B lymphoblastic leukemia lymphoma with t(v;11q23); MLL rearranged (disorder)", "B lymphoblastic leukemia lymphoma with t(v;11q23); MLL rearranged (diagnosis)", "B lymphoblastic leukemia lymphoma with t(v;11q23); MLL rearranged (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-lymphoblastic leukemia/lymphoma with t(v;11q23.3)", "shortest_name_length": 51}
{"curie": "MONDO:0011243", "names": ["GRNG", "Grange syndrome", "GRANGE SYNDROME", "grange syndrome", "grange occlusive arterial syndrome", "Grange Occlusive Arterial Syndrome", "Grange occlusive arterial syndrome", "GRANGE OCCLUSIVE ARTERIAL SYNDROME", "Progressive arterial occlusive disease-hypertension-heart defects-bone fragility-brachysyndactyly syndrome", "progressive arterial occlusive disease-hypertension-heart defects-bone fragility-brachysyndactyly syndrome", "Progressive arterial occlusive disease, hypertension, heart defect, bone fragility, brachysyndactyly syndrome", "Arterial Occlusive Disease, Progressive, with Hypertension, Heart Defects, Bone Fragility, and Brachysyndactyly", "ARTERIAL OCCLUSIVE DISEASE, PROGRESSIVE, WITH HYPERTENSION, HEART DEFECTS, BONE FRAGILITY, AND BRACHYSYNDACTYLY", "arterial occlusive disease, progressive, with hypertension, heart defects, bone fragility, and brachysyndactyly", "Progressive arterial occlusive disease, hypertension, heart defect, bone fragility, brachysyndactyly syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "grange syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0021023", "names": ["CAIS", "MORRIS SYNDROME", "morris syndrome", "Goldberg-Maxwell", "hairless pseudofemale", "testicle; feminization", "feminization; testicle", "testicular feminisation", "Testicular feminization", "Hairless woman syndrome", "feminization testicular", "testicular feminization", "HAIRLESS WOMEN SYNDROME", "Testicular Feminization", "Testicular feminisation", "Goldberg-Morris syndrome", "Feminization, Testicular", "Testicular Feminizations", "Feminizations, Testicular", "GOLDBERG-MAXWELL SYNDROME", "Goldberg-Maxwell Syndrome", "Goldberg-Maxwell syndrome", "androgen receptor deficiency", "Testicular feminization, NOS", "Syndrome of feminizing testes", "Syndrome of feminising testes", "Complete androgen insensitivity", "complete androgen insensitivity", "Testicular Feminization Syndrome", "ANDROGEN INSENSITIVITY, COMPLETE", "testicular feminisation syndrome", "Testicular feminization syndrome", "Testicular feminisation syndrome", "TESTICULAR FEMINIZATION SYNDROME", "testicular feminization syndrome", "feminization syndrome testicular", "Testicular Feminization Syndromes", "Feminization Syndrome, Testicular", "androgen receptor (AR) deficiency", "syndrome; testicular feminization", "testicular feminization; syndrome", "feminization syndromes testicular", "Feminization Syndrome (Testicular)", "Testicular feminization (disorder)", "Feminization Syndromes, Testicular", "complete testicular feminization s", "testicular feminization (diagnosis)", "complete feminizing testes syndrome", "complete androgen resistance syndrome", "Complete androgen resistance syndrome", "testicular feminization (TFM) syndrome", "TFM - Testicular feminization syndrome", "TFM - Testicular feminisation syndrome", "dihydrotestosterone receptor deficiency", "Complete Androgen-Insensitivity Syndrome", "Complete androgen insensitivity syndrome", "Complete Androgen Insensitivity Syndrome", "complete androgen insensitivity syndrome", "Complete Androgen-Insensitivity Syndromes", "Androgen Insensitivity Syndrome, Complete", "androgen insensitivity syndrome, complete", "Androgen-Insensitivity Syndrome, Complete", "Androgen-Insensitivity Syndromes, Complete", "dihydrotestosterone receptor (DHTR) deficiency", "complete androgen insensitivity syndrome (CAIS)", "Complete androgen insensitivity syndrome (disorder)", "complete androgen insensitivity syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complete androgen insensitivity syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0011368", "names": ["Papillary microcarcinoma", "Papillary Thyroid Microcarcinoma", "papillary thyroid Microcarcinoma", "PAPILLARY THYROID MICROCARCINOMA", "Thyroid Gland Papillary Microcarcinoma", "Papillary Thyroid Gland Microcarcinoma", "thyroid gland papillary Microcarcinoma", "papillary thyroid gland Microcarcinoma", "Papillary Microcarcinoma of the Thyroid", "papillary Microcarcinoma of the thyroid", "papillary microcarcinoma of thyroid gland", "papillary Microcarcinoma of the thyroid gland", "papillary microcarcinoma of the thyroid gland", "Papillary Microcarcinoma of the Thyroid Gland", "papillary microcarcinoma of the thyroid gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papillary thyroid Microcarcinoma", "shortest_name_length": 24}
{"curie": "UMLS:C1333293", "names": ["Diffuse Large B-Cell Lymphoma PTLD", "Diffuse Large B-Cell Lymphoma Post-Transplant Lymphoproliferative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse Large B-Cell Lymphoma Post-Transplant Lymphoproliferative Disorder", "shortest_name_length": 34}
{"curie": "UMLS:C3203457", "names": ["Procedural bleeding", "Procedural hemorrhage", "Procedural haemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Procedural hemorrhage", "shortest_name_length": 19}
{"curie": "UMLS:C4324524", "names": ["Intercepted product preparation error"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intercepted product preparation error", "shortest_name_length": 37}
{"curie": "UMLS:C4054577", "names": ["Malignant Mixed Tumor, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Mixed Tumor, Not Otherwise Specified", "shortest_name_length": 46}
{"curie": "MONDO:0023581", "names": ["Kuster syndrome", "cleft lip palate lip pits limb deficiency", "cleft lip and palate, lower lip pits, and limb deficiency defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kuster syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0003751", "names": ["Germ Cell Tumor", "germ cell tumor", "Childhood Germ Cell Tumor", "Pediatric Germ Cell Tumor", "childhood germ cell tumor", "Childhood germ cell tumor", "pediatric germ cell tumor", "childhood germ cell cancer", "pediatric germ cell cancer", "paediatric germ cell cancer", "Childhood Germ Cell Neoplasm", "Pediatric Germ Cell Neoplasm", "pediatric germ cell neoplasm", "childhood germ cell neoplasm", "paediatric germ cell neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood germ cell tumor", "shortest_name_length": 15}
{"curie": "UMLS:C5420267", "names": ["PIGA Deficiency", "PIGA GPI Anchor Protein Defect", "PIGA GPI Anchor Protein Deficiency", "Phosphatidylinositol N-Acetylglucosaminyltransferase Subunit A Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PIGA Deficiency", "shortest_name_length": 15}
{"curie": "UMLS:C0584960", "names": ["Factor V Leiden", "leiden mutation factor v", "Factor V Leiden Mutation", "factor v leiden mutation", "factor V Leiden mutation", "Factor 5 Leiden mutation", "Factor V Leiden mutation", "factor leiden mutation v", "Factor V Leiden mutation (disorder)", "factor V Leiden mutation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Factor V Leiden mutation", "shortest_name_length": 15}
{"curie": "UMLS:C3854396", "names": ["Chronic myeloid leukemia recurrent", "Chronic myeloid leukaemia recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic myeloid leukemia recurrent", "shortest_name_length": 34}
{"curie": "MONDO:0015780", "names": ["DC", "DKC", "DKCD", "MONDO:DC", "Cole syndrome", "Engman syndrome", "Zinsser syndrome", "dyskeratosis congenita", "Dyskeratosis Congenita", "Dyskeratosis congenita", "congenita dyskeratosis", "dyskeratosis congenital", "Congenital dyskeratosis", "congenital dyskeratosis", "dyskeratosis; congenital", "congenital; dyskeratosis", "DKC - Dyskeratosis congenita", "zinsser-cole-engman syndrome", "Zinsser-Cole-Engman syndrome", "Zinsser-Engman-Cole syndrome", "Zinsser-Engman-Cole Syndrome", "Zinsser Cole Engman syndrome", "Hoyeraal-Hreidarsson syndrome", "Cole-Engmann-Zinsser syndrome", "Zinsser-Cole-Engmann syndrome", "dyskeratosis congenita syndrome", "Dyskeratosis congenita syndrome", "Cole-Rauschkolb-Toomey syndrome", "dyskeratosis congenita (DC, DKC)", "Dyskeratosis congenita (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyskeratosis congenita", "shortest_name_length": 2}
{"curie": "MONDO:0008575", "names": ["Tabagism", "tabagism", "Tabaquism", "tobacco abuse", "abuse tobacco", "Tobacco abuse", "TOBACCO ABUSE", "Abuse;tobacco", "Tobacco Abuse", "tobacco; abuse", "abuse; tobacco", "RNDx tobacco abuse", "Tobacco Dependence", "Nicotine Addiction", "Addiction;nicotine", "nicotine addiction", "TOBACCO DEPENDENCE", "tobacco dependence", "Tobacco dependence", "Nicotine addiction", "addiction nicotine", "Dependence;tobacco", "dependence tobacco", "dependence nicotine", "Nicotine Dependence", "Dependence, Tobacco", "nicotine dependence", "Nicotine dependence", "dependence; tobacco", "addictions nicotine", "tobacco; dependence", "nicotine; dependence", "tobacco use disorder", "Tobacco Use Disorder", "dependence; nicotine", "Dependence, Nicotine", "Tobacco use disorder", "Tobacco-Use Disorder", "Disorder, Tobacco-Use", "Disorder, Tobacco Use", "Tobacco Use Disorders", "Dependency on nicotine", "TOBACCO ABUSE UNSPECIFIED", "tobacco abuse (diagnosis)", "Tobacco dependence syndrome", "RNDx tobacco abuse (diagnosis)", "Nicotine dependence (disorder)", "nicotine dependence (diagnosis)", "Compulsive tobacco user syndrome", "tobacco use disorder (diagnosis)", "Nicotine dependence, unspecified", "nicotine dependence tobacco product", "Tobacco dependence syndrome (disorder)", "nicotine dependence tobacco product (diagnosis)", "Mental and behavioral disorders due to use of tobacco, dependence syndrome", "Mental and behavioural disorders due to use of tobacco, dependence syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nicotine dependence", "shortest_name_length": 8}
{"curie": "MONDO:0022758", "names": ["Mosaic Monosome 22", "Mosaic monosome 22", "chromosome 22 mosaic monosomy", "Chromosome 22 mosaic monosomy", "Chromosome 22, monosome mosaic", "chromosome 22, monosome mosaic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 22, monosome mosaic", "shortest_name_length": 18}
{"curie": "MONDO:0012578", "names": ["AUTS13", "autism susceptibility 13", "AUTISM, SUSCEPTIBILITY TO, 13", "autism, susceptibility to, 13"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autism, susceptibility to, 13", "shortest_name_length": 6}
{"curie": "MONDO:0017388", "names": ["Dunbar syndrome", "celiac trunk compression syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "celiac trunk compression syndrome", "shortest_name_length": 15}
{"curie": "UMLS:C1336270", "names": ["Stage III Skin Cancer", "Skin Cancer Stage III", "Stage III Skin Carcinoma", "Skin Carcinoma Stage III", "Carcinoma of Skin Stage III", "Stage III Skin Cancer AJCC v7", "Carcinoma of the Skin Stage III", "stage III nonmelanoma skin cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Skin Cancer", "shortest_name_length": 21}
{"curie": "MONDO:0004534", "names": ["Breast Microglandular Adenosis", "breast microglandular adenosis", "Microglandular Adenosis of Breast", "microglandular adenosis of breast", "Microglandular Adenosis of the Breast", "microglandular adenosis of the breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microglandular adenosis of breast", "shortest_name_length": 30}
{"curie": "MONDO:0011519", "names": ["DFNA23", "DFNA 23", "autosomal dominant deafness 23", "deafness, autosomal dominant 23", "Deafness, Autosomal Dominant 23", "DEAFNESS, AUTOSOMAL DOMINANT 23", "deafness, autosomal dominant type 23", "autosomal dominant nonsyndromic deafness 23", "SIX1 autosomal dominant nonsyndromic deafness", "autosomal dominant nonsyndromic hearing loss 23", "autosomal dominant nonsyndromic deafness type 23", "deafness, autosomal dominant nonsyndromic sensorineural 23", "autosomal dominant nonsyndromic deafness caused by mutation in SIX1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 23", "shortest_name_length": 6}
{"curie": "MONDO:0006045", "names": ["ovary clear cell adenocarcinoma", "Ovarian Clear Cell Adenocarcinoma", "ovarian clear cell adenocarcinoma", "Ovarian clear cell adenocarcinoma", "clear cell adenocarcinoma of ovary", "Clear cell adenocarcinoma of ovary", "Clear cell adenocarcinoma of the ovary", "clear cell adenocarcinoma of the ovary", "Clear cell adenocarcinoma of ovary (disorder)", "clear cell adenocarcinoma of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian clear cell adenocarcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0017091", "names": ["Bilateral polymicrogyria", "bilateral polymicrogyria", "Bilateral polymicrogyria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bilateral polymicrogyria", "shortest_name_length": 24}
{"curie": "UMLS:C0349422", "names": ["steal syndrome", "Steal syndrome", "Steal Syndrome", "stealing syndrome", "arterial steal syndrome", "Arterial steal syndrome", "Vascular access steal syndrome", "Dialysis Access Steal Syndrome", "Vascular Access Steal Syndrome", "Arterial steal syndrome (disorder)", "arterial steal syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arterial steal syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C0859023", "names": ["Talkativeness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Talkativeness", "shortest_name_length": 13}
{"curie": "MONDO:0033561", "names": ["DEEAH", "deeah syndrome", "DEEAH SYNDROME", "Developmental Delay With Endocrine, Exocrine, Autonomic, and Hematologic Abnormalities", "DEVELOPMENTAL DELAY WITH ENDOCRINE, EXOCRINE, AUTONOMIC, AND HEMATOLOGIC ABNORMALITIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deeah syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C3827677", "names": ["Uterine Carcinosarcoma, Homologous Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Carcinosarcoma, Homologous Type", "shortest_name_length": 39}
{"curie": "MONDO:0006195", "names": ["Endometrial polyp", "polyp endometrial", "endometrium polyp", "endometrial polyp", "Polyp endometrial", "ENDOMETRIAL POLYP", "Endometrium polyp", "Endometrial Polyp", "polyp endometrium", "polyps endometrial", "endometrium polyps", "polyp; endometrial", "ENDOMETRIUM, POLYP", "endometrium; polyp", "endometrial polyps", "Endometrial adenoma", "endometrial adenoma", "polyp of endometrium", "Polyp of endometrium", "Polyp(s);endometrial", "Polyp of Endometrium", "Polyp of the Endometrium", "polyp of the endometrium", "endometrial stromal polyp", "Endometrial Stromal Polyp", "endometrial polyps (diagnosis)", "Polyp of endometrium (disorder)", "polyp, endometrial stromal, benign", "POLYP, ENDOMETRIAL STROMAL, BENIGN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometrial polyp", "shortest_name_length": 17}
{"curie": "UMLS:C1707742", "names": ["Diffuse Large B-Cell Lymphoma, Not Otherwise Specified by Gene Expression Profile"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse Large B-Cell Lymphoma, Not Otherwise Specified by Gene Expression Profile", "shortest_name_length": 81}
{"curie": "UMLS:C3273007", "names": ["Benign Liver and Intrahepatic Bile Duct Epithelial Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Liver and Intrahepatic Bile Duct Epithelial Neoplasm", "shortest_name_length": 59}
{"curie": "UMLS:C4725945", "names": ["Lynch-Like Syndrome", "Mutation-Negative Lynch Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mutation-Negative Lynch Syndrome", "shortest_name_length": 19}
{"curie": "MONDO:0019287", "names": ["Dysplasia;ectodermal", "Ectodermal Dysplasia", "dysplasia ectodermal", "Ectodermal dysplasia", "ectodermal dysplasia", "Ectodermal Dysplasias", "Dysplasia, Ectodermal", "ECTODERMAL DYSPLASIAS", "dysplasia; ectodermal", "ectodermal dysplasias", "ectodermal; dysplasia", "Dysplasias, Ectodermal", "Ectodermal dysplasia, NOS", "Congenital Ectodermal Defect", "congenital ectodermal defect", "Congenital ectodermal defect", "Defect, Congenital Ectodermal", "Ectodermal Defect, Congenital", "Congenital Ectodermal Defects", "ectodermal dysplasia syndrome", "Ectodermal dysplasia syndrome", "Ectodermal Dysplasia Syndromes", "Ectodermal Defects, Congenital", "Defects, Congenital Ectodermal", "Ectodermal dysplasia (disorder)", "congenital ectodermal dysplasia", "Congenital ectodermal dysplasia", "ectodermal dysplasia (diagnosis)", "ectodermal dysplasia (select examples)", "Congenital ectodermal defect (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia syndrome", "shortest_name_length": 20}
{"curie": "UMLS:C0855082", "names": ["Refractory Hodgkin Lymphoma", "Refractory Hodgkin lymphoma", "Refractory Hodgkin's Disease", "Refractory Hodgkin's disease", "Hodgkin's disease refractory", "Refractory Hodgkin's Lymphoma", "Refractory Hodgkin's lymphoma", "Hodgkin's disease NOS refractory", "Refractory Hodgkin lymphoma (disorder)", "Refractory Hodgkin lymphoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Hodgkin Lymphoma", "shortest_name_length": 27}
{"curie": "UMLS:C0860564", "names": ["syndrome retinoic acid", "Retinoic acid syndrome", "Retinoic Acid Syndrome", "retinoic acid syndrome", "Differentiation Syndrome", "Differentiation syndrome", "APL Differentiation Syndrome", "Retinoic acid syndrome (diagnosis)", "drug-related disorder retinoic acid syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retinoic acid syndrome", "shortest_name_length": 22}
{"curie": "MONDO:0004006", "names": ["Rete Ovarii Cystadenofibroma", "rete ovarii cystadenofibroma", "cystadenofibroma of rete ovarii"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rete ovarii cystadenofibroma", "shortest_name_length": 28}
{"curie": "MONDO:0004458", "names": ["Bladder Mixed Adenocarcinoma", "bladder mixed adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder mixed adenocarcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0002416", "names": ["Ethmoid Sinus Epidermoid Carcinoma", "ethmoid sinus epidermoid carcinoma", "Ethmoidal Sinus Epidermoid Carcinoma", "ethmoidal sinus epidermoid carcinoma", "epidermoid carcinoma of ethmoid sinus", "Epidermoid Carcinoma of Ethmoid Sinus", "Ethmoid Sinus Squamous Cell Carcinoma", "ethmoid sinus squamous cell carcinoma", "Ethmoidal Sinus Squamous Cell Carcinoma", "ethmoidal sinus squamous cell carcinoma", "Epidermoid Carcinoma of Ethmoidal Sinus", "epidermoid carcinoma of ethmoidal sinus", "squamous cell carcinoma of ethmoid sinus", "Squamous Cell Carcinoma of Ethmoid Sinus", "Epidermoid Carcinoma of the Ethmoid Sinus", "epidermoid carcinoma of the ethmoid sinus", "Squamous cell carcinoma of ethmoidal sinus", "Squamous Cell Carcinoma of Ethmoidal Sinus", "squamous cell carcinoma of ethmoidal sinus", "Epidermoid carcinoma of the ethmoidal sinus", "epidermoid carcinoma of the ethmoidal sinus", "Epidermoid Carcinoma of the Ethmoidal Sinus", "Squamous Cell Carcinoma of the Ethmoid Sinus", "squamous cell carcinoma of the ethmoid sinus", "squamous cell carcinoma of the ethmoidal sinus", "Squamous Cell Carcinoma of the Ethmoidal Sinus", "Primary squamous cell carcinoma of ethmoidal sinus", "Squamous cell carcinoma of ethmoidal sinus (disorder)", "Squamous cell carcinoma of ethmoidal sinus (diagnosis)", "Primary squamous cell carcinoma of ethmoidal sinus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ethmoid sinus squamous cell carcinoma", "shortest_name_length": 34}
{"curie": "UMLS:C2985234", "names": ["Meningeal Malignant Hemangiopericytoma", "Meningeal Anaplastic Hemangiopericytoma", "Meningeal CNS Solitary Fibrous Tumor, Grade 3", "Meningeal Anaplastic Hemangiopericytoma (WHO Grade III)", "Meningeal Solitary Fibrous Tumor/Hemangiopericytoma, Grade 3", "Meningeal Central Nervous System Solitary Fibrous Tumor, Grade 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meningeal Central Nervous System Solitary Fibrous Tumor, Grade 3", "shortest_name_length": 38}
{"curie": "MONDO:0010479", "names": ["CMTX6", "CMT6X", "X-linked Charcot-Marie-Tooth disease type 6", "Charcot-Marie-Tooth disease X-linked dominant 6", "CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 6", "Charcot-Marie-Tooth disease, X-linked dominant, 6", "Charcot-Marie-Tooth neuropathy X-linked dominant 6", "Charcot-Marie-Tooth disease X-linked dominant type 6", "Charcot-Marie-Tooth neuropathy, X-linked dominant, 6", "CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED DOMINANT, 6", "X-linked Charcot-Marie-Tooth disease type 6 (disorder)", "Charcot-Marie-Tooth disease, X-linked dominant, type 6", "Charcot-Marie-Tooth disease, X-linked dominant, 6, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease X-linked dominant 6", "shortest_name_length": 5}
{"curie": "MONDO:0018309", "names": ["HSCR", "megacolon", "Megacolon", "MEGACOLON", "Megacolons", "colectasia", "megarectum", "Macrocolon", "Colectasia", "macrocolon", "Hirschsprung", "aganglionosis", "Megacolon NOS", "Colon dilated", "Aganglionosis", "Enlarged colon", "Dilation of colon", "COLON ENLARGEMENT", "dilatation; colon", "colon; dilatation", "acquired megacolon", "Dilatation of colon", "COLON NOS DILATATION", "HIRSCHSPRUNG DISEASE", "Hirschsprung disease", "congenital megacolon", "megacolon congenital", "disease hirschsprung", "Megacolon;congenital", "MEGACOLON CONGENITAL", "Congenital Megacolon", "Hirshsprungs disease", "hirschsprung disease", "Congenital megacolon", "Hirschsprung Disease", "Megacolon congenital", "idiopathic megacolon", "aganglionic megacolon", "diseases hirschsprung", "Hirschsprungs disease", "pelvirectal achalasia", "megacolon (diagnosis)", "Disease;Hirschsprungs", "disease hirschsprungs", "megacolon; congenital", "hirschsprungs disease", "Disease, Hirschsprung", "Pelvirectal achalasia", "Aganglionic Megacolon", "Hirschsprungs Disease", "Megacolon, Congenital", "Aganglionic megacolon", "MEGACOLON, CONGENITAL", "congenital; megacolon", "Colonic aganglionosis", "macrocolon (diagnosis)", "Megacolon, Aganglionic", "hirschsprung's disease", "disease hirschsprung's", "MEGACOLON, AGANGLIONIC", "Hirschsprung's disease", "Hirschsprung megacolon", "Hirschsprung's Disease", "megacolon; Hirschsprung", "Hirschsprung; megacolon", "Disease, Hirschsprung's", "HD - Hirschsprung's disease", "total intestinal aganglionosis", "Congenital aganglionic megacolon", "Hirschsprung's disease (disorder)", "aganglionic megacolon (diagnosis)", "Congenital (aganglionic) megacolon", "Enlarged colon lacking nerve cells", "congenital intestinal aganglionosis", "Hirschsprung disease susceptibility", "Congenital Intestinal Aganglionosis", "Congenital intestinal aganglionosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hirschsprung disease", "shortest_name_length": 4}
{"curie": "MONDO:0014765", "names": ["ARWH3", "KRT25 woolly hair (disease)", "autosomal recessive woolly hair 3", "woolly hair, autosomal recessive 3", "WOOLLY HAIR, AUTOSOMAL RECESSIVE 3", "woolly hair, autosomal recessive type 3", "woolly hair (disease) caused by mutation in KRT25", "WOOLLY HAIR, AUTOSOMAL RECESSIVE 3, WITH HYPOTRICHOSIS", "woolly hair, autosomal recessive 3, with hypotrichosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "woolly hair, autosomal recessive 3", "shortest_name_length": 5}
{"curie": "MONDO:0011257", "names": ["CDG1B", "CDGIb", "CDG-Ib", "CDG Ib", "CDG 1B", "MPI-CDG", "SLSJ SYNDROME", "Slsj syndrome", "SLSJ syndrome", "MPI DEFICIENCY", "Mpi deficiency", "MPI-CDG (CDG-Ib)", "CDG syndrome type Ib", "CDG syndrome type IB", "CDG gastrointestinal type", "CDG, GASTROINTESTINAL TYPE", "CDG, gastrointestinal type", "Deficiency of phosphohexomutase", "Saguenay-Lac Saint-Jean syndrome", "Saguenay Lac Saint Jean syndrome", "SAGUENAY-LAC SAINT-JEAN SYNDROME", "Deficiency of phosphohexoisomerase", "Phosphomannose isomerase deficiency", "phosphomannose isomerase deficiency", "MANNOSEPHOSPHATE ISOMERASE DEFICIENCY", "Mannosephosphate isomerase deficiency", "Deficiency of phosphomannose isomerase", "congenital disorder of glycosylation Ib", "congenital disorder of glycosylation 1b", "MPI-congenital disorder of glycosylation", "Deficiency of mannose-6-phosphate isomerase", "Congenital disorder of glycosylation type 1B", "Congenital disorder of glycosylation type 1b", "congenital disorder of glycosylation type IB", "congenital disorder of glycosylation type 1b", "Congenital disorder of glycosylation type Ib", "congenital disorder of glycosylation, type IB", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ib", "carbohydrate deficient glycoprotein syndrome type IB", "Protein-losing enteropathy-hepatic fibrosis syndrome", "carbohydrate-deficient glycoprotein syndrome type 1B", "Carbohydrate-deficient glycoprotein syndrome type 1B", "Carbohydrate deficient glycoprotein syndrome type Ib", "PROTEIN-LOSING ENTEROPATHY-HEPATIC FIBROSIS SYNDROME", "Deficiency of mannose-6-phosphate isomerase (disorder)", "Mannosephosphate isomerase congenital disorder of glycosylation", "Mannose-6-phosphate isomerase congenital disorder of glycosylation", "MPI-CDG - mannosephosphate isomerase congenital disorder of glycosylation", "Mannosephosphate isomerase congenital disorder of glycosylation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MPI-congenital disorder of glycosylation", "shortest_name_length": 5}
{"curie": "MONDO:0033556", "names": ["MDDGB15", "congenital muscular dystrophy DPM3-related", "MUSCULAR DYSTROPHY, CONGENITAL, DPM3-RELATED", "Muscular Dystrophy, Congenital, Dpm3-Related", "muscular dystrophy-dystroglycanopathy type B15", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH IMPAIRED INTELLECTUAL DEVELOPMENT), TYPE B, 15", "muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type b, 15"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type b, 15", "shortest_name_length": 7}
{"curie": "UMLS:C4683425", "names": ["II Under Years", "Stage II Thyroid Gland Papillary Cancer Under 55 Years", "Stage II Thyroid Gland Papillary Carcinoma Under 55 Years AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Thyroid Gland Papillary Carcinoma Under 55 Years AJCC v8", "shortest_name_length": 14}
{"curie": "MONDO:0006085", "names": ["Angiolipoma", "angiolipoma", "Angiolipomas", "angiolipomas", "Angiolipoma NOS", "Angiolipoma, NOS", "ANGIOLIPOMA, BENIGN", "angiolipoma, benign", "Cutaneous angiolipomas", "Angiolipoma (disorder)", "adipose tissue angiolipoma", "angiolipoma of fatty tissue", "Angiolipoma (morphologic abnormality)", "angiolipoma of fatty tissue (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angiolipoma", "shortest_name_length": 11}
{"curie": "MONDO:0032812", "names": ["DEE78", "EIEE78", "early infantile epileptic encephalopathy 78", "developmental and epileptic encephalopathy 78", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 78", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 78", "epileptic encephalopathy, early infantile, 78", "developmental and epileptic encephalopathy, 78"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 78", "shortest_name_length": 5}
{"curie": "MONDO:0019447", "names": ["atypical lichen myxedematosus", "Atypical lichen myxedematosus", "Atypical lichen myxoedematosus", "Intermediate lichen myxedematosus", "Intermediate lichen myxoedematosus", "Atypical lichen myxedematosus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical lichen myxedematosus", "shortest_name_length": 29}
{"curie": "UMLS:C4688318", "names": ["Refractory Colorectal Cancer", "Refractory Colorectal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Colorectal Carcinoma", "shortest_name_length": 28}
{"curie": "UMLS:C0043250", "names": ["Wound", "wound", "WOUND", "WOUNDS", "wounds", "Wounds", "Wound NOS", "Wound, NOS", "Flesh wound", "Injury wounds", "injuries wound", "physical wound", "Traumatic Wound", "Wound (disorder)", "morphology wound", "Wound - morphology", "Wound (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury wounds", "shortest_name_length": 5}
{"curie": "MONDO:0011284", "names": ["ASTIGMATISM", "Astigmatism", "astigmatism", "Astigmatism, NOS", "obsolete_astigmatism", "astigmatism (disease)", "Astigmatism (disorder)", "Unspecified astigmatism", "astigmatism (diagnosis)", "Astigmatism, unspecified", "Abnormal curving of the cornea or lens of the eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "astigmatism", "shortest_name_length": 11}
{"curie": "MONDO:0016499", "names": ["Acute pandysautonomia", "acute pandysautonomia", "Acute panautonomic GBS", "acute panautonomic GBS", "Acute panautonomic neuropathy", "acute panautonomic neuropathy", "Acute panautonomic neuropathy (disorder)", "acute panautonomic Guillain-Barré syndrome", "Acute panautonomic Guillain-Barré syndrome", "acute panautonomic Guillain-BarrC) syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute pandysautonomia", "shortest_name_length": 21}
{"curie": "UMLS:C3641117", "names": ["Congenital Reproductive System Abnormality", "Congenital Abnormality of the Reproductive System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Reproductive System Abnormality", "shortest_name_length": 42}
{"curie": "MONDO:0022022", "names": ["BP", "Bowenoid papulosis", "bowenoid papulosis", "Bowenoid Papulosis", "Bowenoid papulosis (disorder)", "Bowenoid papulosis (diagnosis)", "Bowenoid papulosis (morphologic abnormality)", "human papilloma virus-associated intraepithelial neoplasia bowenoid papulosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bowenoid papulosis", "shortest_name_length": 2}
{"curie": "UMLS:C4553877", "names": ["IVB", "Stage IVB Thyroid Gland Papillary Cancer", "Stage IVB Thyroid Gland Papillary Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Thyroid Gland Papillary Carcinoma AJCC v8", "shortest_name_length": 3}
{"curie": "MONDO:0100203", "names": ["parainfluenza 1 infection", "human respirovirus 1 infectious disease", "infection due to human parainfluenza virus 1", "parainfluenza virus type 1 infectious disease", "infection caused by human parainfluenza virus 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parainfluenza virus type 1 infectious disease", "shortest_name_length": 25}
{"curie": "MONDO:0030898", "names": ["IMD76", "immunodeficiency 76", "IMMUNODEFICIENCY 76", "immunodeficiency due to FCHO1 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 76", "shortest_name_length": 5}
{"curie": "UMLS:C2986869", "names": ["Ectopic Cervical Thymoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ectopic Cervical Thymoma", "shortest_name_length": 24}
{"curie": "MONDO:0007552", "names": ["DEB-Pt", "pretibial DEB", "DEB, PRETIBIAL", "Deb, pretibial", "PRETIBIAL BLISTER", "Pretibial blistering", "Localized DEB, pretibial form", "Pretibial epidermolysis bullosa", "pretibial epidermolysis bullosa", "Epidermolysis bullosa, pretibial", "epidermolysis bullosa, pretibial", "EPIDERMOLYSIS BULLOSA, PRETIBIAL", "Pretibial dystrophic epidermolysis bullosa", "Pretibial epidermolysis bullosa (disorder)", "pretibial dystrophic epidermolysis bullosa", "Dystrophic Epidermolysis Bullosa, Pretibial", "dystrophic epidermolysis bullosa, pretibial", "DYSTROPHIC EPIDERMOLYSIS BULLOSA, PRETIBIAL", "epidermolysis bullosa dystrophica, pretibial", "Epidermolysis Bullosa Dystrophica, Pretibial", "EPIDERMOLYSIS BULLOSA DYSTROPHICA, PRETIBIAL", "Localized dystrophic epidermolysis bullosa, pretibial form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pretibial dystrophic epidermolysis bullosa", "shortest_name_length": 6}
{"curie": "MONDO:0009617", "names": ["MCPH1", "PCC SYNDROME", "PCC syndrome", "primary autosomal recessive microcephaly 1", "PREMATURE CHROMOSOME CONDENSATION SYNDROME", "premature chromosome condensation syndrome", "Premature Chromosome Condensation Syndrome", "Microcephaly, Primary Autosomal Recessive, 1", "microcephaly 1, primary, autosomal recessive", "MICROCEPHALY, PRIMARY AUTOSOMAL RECESSIVE, 1", "MICROCEPHALY 1, PRIMARY, AUTOSOMAL RECESSIVE", "MCPH1 autosomal recessive primary microcephaly", "autosomal recessive primary microcephaly caused by mutation in MCPH1", "premature chromosome condensation with microcephaly and mental retardation", "PREMATURE CHROMOSOME CONDENSATION WITH MICROCEPHALY AND MENTAL RETARDATION", "Premature Chromosome Condensation with Microcephaly and Mental Retardation", "premature chromosome condensation with microcephaly and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly 1, primary, autosomal recessive", "shortest_name_length": 5}
{"curie": "UMLS:C0856099", "names": ["Hemorrhoids aggravated", "Haemorrhoids aggravated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Haemorrhoids aggravated", "shortest_name_length": 22}
{"curie": "MONDO:0015097", "names": ["aortic valve dysplasia", "Aortic valve dysplasia", "Mucoid thickening of aortic valve", "Aortic valve dysplasia (disorder)", "Aortic valve dysplasia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic valve dysplasia", "shortest_name_length": 22}
{"curie": "MONDO:0034661", "names": ["syndromic biliary atresia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic biliary atresia", "shortest_name_length": 25}
{"curie": "MONDO:0005150", "names": ["AMD", "ARMD", "macular degeneration", "Macular Degeneration", "Age-Related Maculopathy", "Age Related Maculopathy", "age-related maculopathy", "age related maculopathy", "Maculopathy, Age-Related", "Maculopathy, Age Related", "MACULOPATHY, AGE-RELATED", "Age Related Maculopathies", "Age-Related Maculopathies", "age related Maculopathies", "Maculopathies, Age-Related", "senile macular degeneration", "Senile macular degeneration", "Macular degeneration senile", "age related macular degeneration", "MACULAR DEGENERATION AGE RELATED", "Age-related macular degeneration", "Age-Related Macular Degeneration", "macular degeneration age-related", "Age related macular degeneration", "Age Related Macular Degeneration", "age-related macular degeneration", "Macular Degeneration, Age-Related", "Macular Degeneration, Age Related", "macular degeneration, age-related", "Macular degeneration, age-related", "Age-Related Macular Degenerations", "SMD - Senile macular degeneration", "Senile macular retinal degeneration", "AMD - Age-related macular degeneration", "ARMD - Age-related macular degeneration", "ARMD (age related macular degeneration)", "AAMD - Age related macular degeneration", "age related macular degeneration (ARMD)", "Senile macular retinal degeneration, NOS", "Macular degeneration (senile), unspecified", "Age-related macular degeneration (disorder)", "Age-related macular degeneration (diagnosis)", "Senile macular degeneration of retina, unspecified", "Macular degeneration (senile) of retina, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "age-related macular degeneration", "shortest_name_length": 3}
{"curie": "UMLS:C4521057", "names": ["stage IA vulvar cancer", "Stage IA Vulvar Cancer", "Stage IA Vulvar Carcinoma", "stage IA vulvar carcinoma", "stage IA vulvar cancer AJCC v7", "Stage IA Vulvar Cancer AJCC v7", "Stage IA Vulvar Carcinoma AJCC v7", "stage IA vulvar carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Vulvar Cancer AJCC v7", "shortest_name_length": 22}
{"curie": "UMLS:C4744523", "names": ["Hypothalamic-Chiasmatic Pilomyxoid Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypothalamic-Chiasmatic Pilomyxoid Astrocytoma", "shortest_name_length": 46}
{"curie": "MONDO:0004659", "names": ["Cancer in situ of eye", "eye in situ carcinoma", "eye carcinoma in situ", "stage 0 eye carcinoma", "Carcinoma in situ of eye", "carcinoma in situ of eye", "ocular carcinoma in situ", "carcinoma in situ of eyeball", "Carcinoma in situ of eye, NOS", "Carcinoma in situ of eye (disorder)", "carcinoma in situ of eye (diagnosis)", "carcinoma in situ of eyeball (diagnosis)", "stage 0 eyeball of camera-type eye carcinoma", "eyeball of camera-type eye carcinoma in situ", "carcinoma in situ of eyeball of camera-type eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eye carcinoma in situ", "shortest_name_length": 21}
{"curie": "UMLS:C4552922", "names": ["IB", "Stage IB Cervical Cancer", "Stage IB Cervical Cancer AJCC v8", "Stage IB Cervical Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Cervical Cancer AJCC v8", "shortest_name_length": 2}
{"curie": "UMLS:C1710105", "names": ["Cavernous nevus of skin", "Cavernous naevus of skin", "Cavernous angioma of skin", "Skin Cavernous Hemangioma", "Cavernous hemangioma of skin", "Cavernous haemangioma of skin", "Cavernous hemangioma of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin Cavernous Hemangioma", "shortest_name_length": 23}
{"curie": "MONDO:0032806", "names": ["TTD7", "nonphotosensitive trichothiodystrophy 7", "TRICHOTHIODYSTROPHY 7, NONPHOTOSENSITIVE", "Trichothiodystrophy 7, Nonphotosensitive", "trichothiodystrophy 7, nonphotosensitive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichothiodystrophy 7, nonphotosensitive", "shortest_name_length": 4}
{"curie": "MONDO:0005709", "names": ["Cold", "cold", "COLD", "colds", "CORYZA", "Coryza", "head cold", "Head cold", "common cold", "Common Cold", "COMMON COLD", "Common cold", "common colds", "cold; common", "Cold, common", "common; cold", "acute coryza", "Common Colds", "Cold, Common", "Acute coryza", "Colds, Common", "Coryza, acute", "RHINITIS ACUTE", "rhinitis acute", "Cold (Disease)", "Head cold, NOS", "Coryza (acute)", "acute rhinitis", "Acute rhinitis", "Rhinitis;acute", "URI (head cold)", "rhinitis; acute", "RHINITIS, ACUTE", "rhino-sinusitis", "acute; rhinitis", "Rhinitis, acute", "Rhinitis infective", "Infective rhinitis", "rhinitis; infective", "Acute nasal catarrh", "Rhinitis, infective", "RHINITIS INFECTIOUS", "Infectious Rhinitis", "infective; rhinitis", "Common cold syndrome", "Nasal catarrh, acute", "Rhinitis (infective)", "Acute nasopharyngitis", "Non-Allergic Rhinitis", "Acute Nasopharyngitis", "Nasopharyngitis;acute", "nasal; catarrh, acute", "catarrh; nasal, acute", "acute nasopharyngitis", "Common cold (disorder)", "Nasopharyngitis, acute", "nasopharyngitis, acute", "Nasopharyngitis - acute", "common cold (diagnosis)", "nasopharyngitis - acute", "Acute infective rhinitis", "Infective nasopharyngitis", "Acute rhinitis (disorder)", "Acute nasopharyngitis, NOS", "acute rhinitis (diagnosis)", "acute viral rhinopharyngitis", "Acute viral rhinopharyngitis", "Infective nasopharyngitis NOS", "nasopharyngeal; catarrh, acute", "Infective rhinitis (diagnosis)", "Infective nasopharyngitis, NOS", "catarrh; nasopharyngeal, acute", "viral upper respiratory infection", "acute nasopharyngitis (diagnosis)", "upper respiratory infection viral", "UPPER RESPIRATORY INFECTION VIRAL", "Upper respiratory infection acute", "VIRAL UPPER RESPIRATORY INFECTION", "Acute nasopharyngitis (common cold)", "acute nasopharyngitis [common cold]", "Acute nasopharyngitis [common cold]", "viral upper respiratory infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "common cold", "shortest_name_length": 4}
{"curie": "MONDO:0020854", "names": ["LIDLS2", "LIDDLE SYNDROME 2", "Liddle syndrome 2", "SCNN1G Liddle syndrome", "Liddle syndrome caused by mutation in SCNN1G"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liddle syndrome 2", "shortest_name_length": 6}
{"curie": "UMLS:C4526915", "names": ["Lung Mucinous Adenocarcinoma In Situ"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Mucinous Adenocarcinoma In Situ", "shortest_name_length": 36}
{"curie": "MONDO:0012586", "names": ["ADCAD2", "CAD autosomal dominant 2", "LRP6 coronary artery disease", "CAD autosomal dominant 2 (diagnosis)", "coronary artery disease autosomal dominant 2", "CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT 2", "Coronary Artery Disease, Autosomal Dominant 2", "coronary artery disease, autosomal dominant 2", "coronary artery disease, autosomal dominant, 2", "coronary artery disease, autosomal dominant type 2", "coronary artery disease caused by mutation in LRP6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coronary artery disease, autosomal dominant 2", "shortest_name_length": 6}
{"curie": "MONDO:0800102", "names": ["ACHM2", "RMCH2", "achromatopsia 2", "rod monochromacy 2", "CNGA3 achromatopsia", "rod monochromatism 2", "achromatopsia type 2", "colorblindness, total", "CNGA3-related retinopathy", "achromatopsia caused by mutation in CNGA3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CNGA3-related retinopathy", "shortest_name_length": 5}
{"curie": "MONDO:0005770", "names": ["genital hsv", "Genital herpes", "GENITAL HERPES", "Genital Herpes", "genital herpes", "Herpes genital", "HERPES GENITAL", "genital; herpes", "genitals herpes", "venereal herpes", "herpes; genital", "Herpes, Genital", "Herpes Genitalis", "herpes genitalis", "HERPES GENITALIA", "Herpes genitalis", "herpes genitalia", "HERPES GENITALIS", "Virus-Genital Herpes", "virus-genital herpes", "genital herpes simplex", "simplex genital herpes", "Genital herpes simplex", "GENITAL HERPES SIMPLEX", "Genital Herpes Simplex", "Herpes Simplex, Genital", "herpes simplex genitalis", "Genital herpes, unspecified", "Genital herpes simplex, NOS", "Genital herpes simplex (disorder)", "genital herpes simplex (diagnosis)", "Herpes Simplex Virus Genital Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genital herpes", "shortest_name_length": 11}
{"curie": "MONDO:0008297", "names": ["VP", "PPOX DEFICIENCY", "PPOX deficiency", "Ppox Deficiency", "Mixed porphyria", "Deficiency, Ppox", "Ppox Deficiencies", "Porphyria Variegate", "PORPHYRIA VARIEGATA", "variegate porphyria", "Protocoproporphyria", "VARIEGATE PORPHYRIA", "Variegate Porphyria", "Variegate porphyria", "porphyria variegata", "Porphyria variegata", "Porphyria Variegata", "porphyria variegate", "porphyria variegated", "PORPHYRIA, VARIEGATE", "porphyria; variegata", "Porphyria, Variegate", "Dean-Barnes syndrome", "variegata; porphyria", "South African porphyria", "Mixed hepatic porphyria", "VP (variegate porphyria)", "South African; porphyria", "porphyria variegata (VP)", "VP - Variegate porphyria", "PORPHYRIA, MIXED HEPATIC", "porphyria; South African", "Porphyria, South African Type", "porphyria, South African type", "PORPHYRIA, SOUTH AFRICAN TYPE", "Variegate porphyria (disorder)", "Protocoproporphyria hereditaria", "South African genetic porphyria", "variegate porphyria (diagnosis)", "PORPHYRIA, SOUTH AFRICAN GENETIC", "PORPHYRIA CUTANEA TARDA HEREDITARIA", "Protoporphyrinogen oxidase deficiency", "PROTOPORPHYRINOGEN OXIDASE DEFICIENCY", "protoporphyrinogen oxidase deficiency", "Protoporphyrinogen Oxidase Deficiency", "porphyria variegata, susceptibility to", "VARIEGATE PORPHYRIA, HOMOZYGOUS VARIANT", "variegate porphyria, homozygous variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "variegate porphyria", "shortest_name_length": 2}
{"curie": "MONDO:0000624", "names": ["benign gynecologic tumor", "Benign Gynecologic Tumor", "GYNECOLOGIC TUMOR BENIGN", "benign gynecologic neoplasm", "Benign Gynecologic Neoplasm", "Benign Female Reproductive System Tumor", "benign female reproductive system tumor", "female reproductive organ benign neoplasm", "benign female reproductive system neoplasm", "Benign Female Reproductive System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign female reproductive system neoplasm", "shortest_name_length": 24}
{"curie": "MONDO:0002888", "names": ["Intraorbital Meningioma", "intraorbital meningioma", "Intraorbital Meningiomas", "Meningioma, Intraorbital", "Meningiomas, Intraorbital"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intraorbital meningioma", "shortest_name_length": 23}
{"curie": "MONDO:0008383", "names": ["ra", "RA", "Rheumatic gout", "gout rheumatic", "Atrophic arthritis", "atrophic Arthritis", "atrophic arthritis", "Rheumatoid disease", "arthritis; atrophic", "atrophic; arthritis", "ARTHRITIS, RHEUMATIC", "Arthritis, rheumatic", "Arthritis rheumatoid", "autoimmune arthritis", "ARTHRITIS RHEUMATOID", "rheumatoid arthritis", "Rheumatoid Arthritis", "RHEUMATOID ARTHRITIS", "Rheumatoid arthritis", "arthritis; rheumatoid", "ARTHRITIS, RHEUMATOID", "Arthritis, Rheumatoid", "rheumatoid; arthritis", "arthritis, rheumatoid", "Proliferative arthritis", "proliferative arthritis", "RA - Rheumatoid arthritis", "RA (rheumatoid arthritis)", "RhA - Rheumatoid arthritis", "Chronic rheumatic arthritis", "Proliferative arthritis, NOS", "rheumatoid arthritis systemic", "Systemic rheumatoid arthritis", "Rheumatoid arthritis (disorder)", "rheumatoid arthritis (diagnosis)", "Rheumatoid arthritis, unspecified", "Arthritis or polyarthritis, atrophic", "rheumatoid arthritis, progression of", "arthritis or polyarthritis, rheumatic", "Arthritis or polyarthritis, rheumatic", "rheumatoid arthritis, susceptibility to", "RHEUMATOID ARTHRITIS, SUSCEPTIBILITY TO", "Rheumatoid arthritis, unspecified, site unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rheumatoid arthritis", "shortest_name_length": 2}
{"curie": "MONDO:0054669", "names": ["PCH11", "pontocerebellar hypoplasia type 11", "Pontocerebellar hypoplasia type 11", "PONTOCEREBELLAR HYPOPLASIA, TYPE 11", "pontocerebellar hypoplasia, type 11", "Pontocerebellar hypoplasia due to TBC1D23"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pontocerebellar hypoplasia, type 11", "shortest_name_length": 5}
{"curie": "MONDO:0013716", "names": ["AAA4", "aortic aneurysm, familial abdominal, 4", "AORTIC ANEURYSM, FAMILIAL ABDOMINAL, 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic aneurysm, familial abdominal, 4", "shortest_name_length": 4}
{"curie": "UMLS:C5206374", "names": ["Advanced Pancreatic Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Pancreatic Adenocarcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0018208", "names": ["neurofibromatosis type 1 due to NF1 mutation or intragenic deletion", "Von Recklinghausen disease due to NF1 mutation or intragenic deletion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurofibromatosis type 1 due to NF1 mutation or intragenic deletion", "shortest_name_length": 67}
{"curie": "UMLS:C5206439", "names": ["Stage IB Cervical Cancer FIGO 2018", "Stage IB Cervical Carcinoma FIGO 2018"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Cervical Cancer FIGO 2018", "shortest_name_length": 34}
{"curie": "UMLS:C0854847", "names": ["Intestinal T-Cell Lymphoma Stage III", "Intestinal T-cell lymphoma stage III", "Stage III Intestinal T-Cell Lymphoma", "Stage III Enteropathy-type T-Cell Lymphoma", "Stage III Enteropathy-Associated T-Cell Lymphoma", "Ann Arbor Stage III Enteropathy-Associated T-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal T-cell lymphoma stage III", "shortest_name_length": 36}
{"curie": "MONDO:0017036", "names": ["histiocytosis X in childhood and adulthood", "Langerhans cell histiocytosis in childhood and adulthood", "Langerhans cell granulomatosis in childhood and adulthood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Langerhans cell histiocytosis in childhood and adulthood", "shortest_name_length": 42}
{"curie": "MONDO:0044619", "names": ["PTU embryopathy", "PTU embryofetopathy", "propylthiouracil embryopathy", "propylthiouracil embryofetopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "propylthiouracil embryofetopathy", "shortest_name_length": 15}
{"curie": "MONDO:0003411", "names": ["breast hemangiopericytoma", "breast spindle cell tumor", "Breast Hemangiopericytoma", "hemangiopericytoma of the breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast hemangiopericytoma", "shortest_name_length": 25}
{"curie": "UMLS:C0011304", "names": ["Myelinolysis", "myelinolysis", "DEMYELINATION", "Demyelination", "Myelinoclasis", "demyelination", "Demyelinations", "Dysmyelination", "Demyelination NOS", "Axon demyelination", "Demyelination, NOS", "Neuronal demyelination", "Demyelination (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Demyelination", "shortest_name_length": 12}
{"curie": "MONDO:0013908", "names": ["TTPP3", "THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 3", "thyrotoxic periodic paralysis, susceptibility to, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyrotoxic periodic paralysis, susceptibility to, 3", "shortest_name_length": 5}
{"curie": "UMLS:C0854792", "names": ["Resectable Bile Duct Cancer", "Bile duct cancer resectable", "Bile Duct Cancer, Resectable", "Resectable Cancer of Bile Duct", "Bile duct carcinoma resectable", "Carcinoma bile duct resectable", "Resectable Cancer of the Bile Duct", "Resectable Extrahepatic Bile Duct Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bile duct cancer resectable", "shortest_name_length": 27}
{"curie": "MONDO:0015591", "names": ["limbic encephalitis associated with antibodies to cell membrane antigens"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "limbic encephalitis associated with antibodies to cell membrane antigens", "shortest_name_length": 72}
{"curie": "MONDO:0006878", "names": ["Moraxella infection", "Moraxella infections", "infection, Moraxella", "infections, Moraxella", "Psychobacter infection", "Moraxellaceae Infection", "Psychobacter infections", "Moraxellaceae infection", "infection, Psychobacter", "infection, Moraxellaceae", "infections, Psychobacter", "Moraxellaceae Infections", "Infection, Moraxellaceae", "infections, Moraxellaceae", "Infections, Moraxellaceae", "Moraxellaceae infectious disease", "Moraxellaceae disease or disorder", "Moraxellaceae caused disease or disorder", "opportunistic Moraxellaceae infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Moraxellaceae infectious disease", "shortest_name_length": 19}
{"curie": "MONDO:0012124", "names": ["SIDDT", "sudden infant death - dysgenesis of the testes", "Sudden infant death-dysgenesis of the testes syndrome", "sudden infant death-dysgenesis of the testes syndrome", "Sudden infant death with dysgenesis of testes syndrome", "SUDDEN INFANT DEATH WITH DYSGENESIS OF THE TESTES SYNDROME", "Sudden Infant Death with Dysgenesis of the Testes Syndrome", "sudden infant death with dysgenesis of the testes syndrome", "Sudden infant death with dysgenesis of testes syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sudden infant death-dysgenesis of the testes syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0021722", "names": ["vulva pain", "pain vulva", "Vulvodynia", "Pain;vulva", "vulvodynia", "Vulvar pain", "vulvar pain", "VULVAR PAIN", "Vulval pain", "vulval pain", "burning vulva", "Vulva painful", "Pain of vulva", "Burning vulva", "vulva burning", "pain of vulva", "vulvar burning", "Vulvodynia NOS", "vulval discomfort", "vulvar discomfort", "Burning (of);vulva", "discomfort of vulva", "vulvar pain (symptom)", "Vulvodynia (disorder)", "Vulval pain (finding)", "vulvodynia (diagnosis)", "Vulvodynia, unspecified", "vulvar burning (symptom)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvodynia", "shortest_name_length": 10}
{"curie": "UMLS:C1333553", "names": ["FIGO Stage IIB GTT", "FIGO Stage IIB Gestational Trophoblastic Tumor", "FIGO Stage IIB Gestational Trophoblastic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Stage IIB Gestational Trophoblastic Tumor", "shortest_name_length": 18}
{"curie": "UMLS:C3805117", "names": ["Rebound psychosis", "Withdrawal psychosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rebound psychosis", "shortest_name_length": 17}
{"curie": "MONDO:0021248", "names": ["nervous system tumor", "Nervous System Tumor", "Nervous System Tumour", "nervous system tumour", "Tumor of Nervous System", "tumor of nervous system", "nervous system neoplasm", "Nervous System Neoplasm", "nervous system neoplasms", "Nervous System Neoplasms", "Neoplasm of Nervous System", "neoplasm of nervous system", "tumor of the nervous system", "Tumor of the Nervous System", "neoplasm of the nervous system", "Neoplasm of the Nervous System", "nervous system neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nervous system neoplasm", "shortest_name_length": 20}
{"curie": "UMLS:C5555171", "names": ["Recurrent Fallopian Tube Mucinous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Fallopian Tube Mucinous Adenocarcinoma", "shortest_name_length": 48}
{"curie": "MONDO:0007330", "names": ["Bipartite clavicle", "Clavicle pseudoarthrosis", "clavicle pseudoarthrosis", "pseudarthrosis; clavicle", "clavicle; pseudarthrosis", "pseudoarthrosis of clavicle", "Pseudoarthrosis of clavicle", "Bipartite clavicle (finding)", "Pseudoarthrosis of the clavicle", "Congenital pseudarthrosis of clavicle", "congenital pseudoarthrosis of clavicle", "Pseudoarthrosis of clavicle (disorder)", "Congenital pseudoarthrosis of clavicle", "clavicle, pseudarthrosis of, congenital", "CLAVICLE, PSEUDARTHROSIS OF, CONGENITAL", "Clavicle, Pseudarthrosis Of, Congenital", "Congenital pseudarthrosis of the clavicle", "congenital pseudarthrosis of the clavicle", "congenital pseudoarthrosis of the clavicle", "Congenital pseudoarthrosis of the clavicle", "Congenital pseudoarthrosis of clavicle (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital pseudoarthrosis of clavicle", "shortest_name_length": 18}
{"curie": "MONDO:0019545", "names": ["systemic monochloroacetate poisoning"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "systemic monochloroacetate poisoning", "shortest_name_length": 36}
{"curie": "UMLS:C0021295", "names": ["infant premature disease", "premature infant diseases", "disease infants premature", "Infant, Premature, Diseases", "Premature infants--Diseases", "disease of premature infants"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infant, Premature, Diseases", "shortest_name_length": 24}
{"curie": "UMLS:C0279587", "names": ["non-T, non-B, cALLa negative childhood ALL", "pediatric ALL, non-T, non-B, cALLA negative", "childhood ALL, non T, non B, cALLa negative", "cALLa negative, non T, non B, childhood ALL", "pediatric ALL, non T, non B, cALLA negative", "ALL, cALLa negative, non-T, non-B childhood", "cALLa negative, non-T, non-B, childhood ALL", "childhood ALL, non-T, non-B, cALLa negative", "ALL, pediatric, non-T, non-B, cALLa negative", "ALL, childhood, non-T, non-B, cALLa negative", "ALL, pediatric, non T, non B, cALLa negative", "ALL, non T, non B, cALLa negative, childhood", "ALL, non-T, non-B, cALLa negative, childhood", "ALL, childhood, non T, non B, cALLa negative", "leukemia, childhood ALL non-T, non-B, cALLa negative", "leukemia, ALL non-T, non-B, cALLa negative, childhood", "Non-T Non-B CALLA Negative Acute Lymphoblastic Leukemia", "non B, non T, cALLa negative childhood acute lymphocytic leukemia", "Non-T Non-B CALLA Negative Childhood Acute Lymphoblastic Leukemia", "non-T, non-B, cALLa negative childhood acute lymphocytic leukemia", "non T, non B, cALLa negative childhood acute lymphocytic leukemia", "non-B, non-T, cALLa negative childhood acute lymphocytic leukemia", "leukemia, childhood acute lymphocytic non-T, non-B, cALLa negative", "acute lymphocytic leukemia, childhood non-T, non-B, cALLa negative", "non-T, non-B, cALLa negative childhood acute lymphoblastic leukemia", "acute lymphoblastic leukemia, childhood non-T, non-B, cALLa negative"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-T Non-B CALLA Negative Childhood Acute Lymphoblastic Leukemia", "shortest_name_length": 42}
{"curie": "MONDO:0008284", "names": ["GAPPS", "Gastric polyposis", "POLYPOSIS, GASTRIC", "Fundic gland polyps", "Fundic Gland Polyposis", "Fundic gland polyposis", "FUNDIC GLAND POLYPOSIS", "fundic gland polyposis", "Polyposis of proximal stomach", "Proximal polyposis of the stomach", "polyposis of gastric fundus without polyposis coli", "Polyposis Of Gastric Fundus Without Polyposis Coli", "POLYPOSIS OF GASTRIC FUNDUS WITHOUT POLYPOSIS COLI", "Familial fundic gland polyposis with gastric cancer", "GASTRIC ADENOCARCINOMA AND PROXIMAL POLYPOSIS OF THE STOMACH", "Gastric adenocarcinoma and proximal polyposis of the stomach"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyposis of gastric fundus without polyposis coli", "shortest_name_length": 5}
{"curie": "MONDO:0017740", "names": ["disorder of protein N-glycosylation", "protein N-linked glycosylation disease", "disorder of protein N-linked glycosylation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of protein N-glycosylation", "shortest_name_length": 35}
{"curie": "UMLS:C5670535", "names": ["Global DNA Hypomethylation", "Global Genomic Hypomethylation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Global DNA Hypomethylation", "shortest_name_length": 26}
{"curie": "UMLS:C1336489", "names": ["Stage I Testicular Nonseminomatous Germ Cell Tumor", "Stage I Testicular Non-Seminomatous Germ Cell Tumor", "Stage I Testicular Non-Seminomatous Germ Cell Tumor AJCC v6", "Stage I Testicular Non-Seminomatous Germ Cell Tumor AJCC v7", "Stage I Testicular Non-Seminomatous Germ Cell Tumor AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Testicular Non-Seminomatous Germ Cell Tumor AJCC v6 and v7", "shortest_name_length": 50}
{"curie": "UMLS:C0152413", "names": ["RSV pneumonia", "Respiratory syncytial virus pneumonia", "Respiratory Syncytial Virus Pneumonia", "Pneumonia respiratory syncytial viral", "respiratory syncytial virus; pneumonia", "pneumonia; respiratory syncytial virus", "viral; pneumonia, respiratory syncytial", "pneumonia; viral, respiratory syncytial", "pneumonia due to respiratory syncytial virus", "Pneumonia due to respiratory syncytial virus", "Pneumonia caused by respiratory syncytial virus", "pneumonia due to respiratory syncytial virus (diagnosis)", "Pneumonia caused by respiratory syncytial virus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pneumonia due to respiratory syncytial virus", "shortest_name_length": 13}
{"curie": "MONDO:0010153", "names": ["Trichoodontoonychial dysplasia", "trichoodontoonychial dysplasia", "Trichoodontoonychial Dysplasia", "Trichoodontoonychial dysplasia (disorder)", "TRICHOODONTOONYCHIAL DYSPLASIA WITH BONE DEFICIENCY", "trichoodontoonychial dysplasia with bone deficiency", "Trichoodontoonychial dysplasia with bone deficiency in frontoparietal region", "trichoodontoonychial dysplasia with bone deficiency in frontoparietal region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichoodontoonychial dysplasia", "shortest_name_length": 30}
{"curie": "MONDO:0007173", "names": ["ASD7", "atrial septal defect 7", "atrial heart septal defect 7", "NKX2-5 atrial heart septal defect", "atrial heart septal defect type 7", "ASD with Atrioventricular Conduction Defects", "atrial heart septal defect caused by mutation in NKX2-5", "ASD with or without atrioventricular conduction defects", "ASD WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS", "atrial septal defect 7, with or without AV conduction defects", "Atrial Septal Defect with Atrioventricular Conduction Defects", "atrial septal defect-atrioventricular conduction defects syndrome", "atrial septal defect 7 with or without atrioventricular conduction defects", "ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial septal defect 7", "shortest_name_length": 4}
{"curie": "UMLS:C4525199", "names": ["Tumor Stage (Pathologic)", "Liver Cell Carcinoma by AJCC v8 Stage", "Hepatocellular Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatocellular Carcinoma by AJCC v8 Stage", "shortest_name_length": 24}
{"curie": "UMLS:C4525615", "names": ["Stage I Duodenal Neuroendocrine Tumor", "Stage I Duodenal Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Duodenal Neuroendocrine Tumor AJCC v8", "shortest_name_length": 37}
{"curie": "MONDO:0006215", "names": ["Gallbladder Adenocarcinoma", "gallbladder adenocarcinoma", "Gallbladder adenocarcinoma", "gall bladder adenocarcinoma", "adenocarcinomas gallbladder", "Adenocarcinoma of Gallbladder", "adenocarcinoma of gallbladder", "adenocarcinoma of the gallbladder", "Adenocarcinoma of the Gallbladder", "gallbladder, adenocarcinoma of the", "gallbladder cancer, adenocarcinoma", "adenocarcinoma of gallbladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gallbladder adenocarcinoma", "shortest_name_length": 26}
{"curie": "UMLS:C1516070", "names": ["Astler-Coller C1 Rectal Carcinoma", "Astler-Coller C1 Carcinoma of Rectum", "Astler-Coller C1 Carcinoma of the Rectum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Astler-Coller C1 Rectal Carcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C5204519", "names": ["Advanced Gastroesophageal Junction Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Gastroesophageal Junction Adenocarcinoma", "shortest_name_length": 49}
{"curie": "UMLS:C1334980", "names": ["Non-Hodgkin Lymphoma with Variable Clinical Course", "Non-Hodgkin's Lymphoma with Variable Clinical Course"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Hodgkin Lymphoma with Variable Clinical Course", "shortest_name_length": 50}
{"curie": "MONDO:0021064", "names": ["Glomus tumor", "jugular body tumor", "Glomus jugular tumor", "glomus jugulare tumor", "Glomus jugular tumors", "jugular paraganglioma", "Jugular Paraganglioma", "Jugular paraganglioma", "Glomus jugulare tumor", "GLOMUS JUGULARE TUMOR", "Glomus Jugulare Tumor", "Glomus jugular tumour", "tumor of jugular body", "jugular body neoplasm", "jugular paragangliomas", "Glomus jugulare tumors", "Glomus jugulare tumour", "GLOMUS JUGULARE TUMORS", "Tumor, Glomus Jugulare", "Glomus Jugulare Tumors", "glomus jugulare tumors", "Jugulare Tumor, Glomus", "tumor; glomus jugulare", "Glomus jugulare--Tumors", "Glomus jugulare tumours", "[M]Glomus jugulare tumor", "tumor of glomus jugulare", "glomus jugulare neoplasm", "Tumor of Glomus Jugulare", "Glomus Jugulare Neoplasm", "neoplasm of jugular body", "[M]Glomus jugulare tumour", "neoplasm of glomus jugulare", "Neoplasm of Glomus Jugulare", "Neoplasm of glomus jugulare", "Jugulotympanic Paraganglioma", "tumor of the glomus jugulare", "jugulotympanic paraganglioma", "Jugulotympanic paraganglioma", "Tumor of the Glomus Jugulare", "jugular body neoplasm (disease)", "Neoplasm of the Glomus Jugulare", "neoplasm of the glomus jugulare", "Paraganglioma - glomus jugulare", "Neoplasm of glomus jugulare (disorder)", "neoplasm of glomus jugulare (diagnosis)", "basicranium parasympathetic paraganglioma", "parasympathetic paraganglioma of basicranium", "Glomus jugulare tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "jugulotympanic paraganglioma", "shortest_name_length": 12}
{"curie": "MONDO:0016947", "names": ["partial trisomy of chromosome 10p", "partial duplication of chromosome 10p", "partial trisomy of the short arm of chromosome 10", "partial duplication of the short arm of chromosome 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of the short arm of chromosome 10", "shortest_name_length": 33}
{"curie": "MONDO:0014506", "names": ["HLD9", "RARS leukodystrophy", "hypomyelinating leukodystrophy 9", "leukodystrophy, hypomyelinating, 9", "LEUKODYSTROPHY, HYPOMYELINATING, 9", "hypomyelinating leukodystrophy type 9", "leukodystrophy, hypomyelinating, type 9", "leukodystrophy caused by mutation in RARS", "RARS-related autosomal recessive hypomyelinating leukodystrophy", "RARS-related autosomal recessive hypomyelinating leucodystrophy", "Arginyl-tRNA synthetase 1-related autosomal recessive hypomyelinating leukodystrophy", "Arginyl-tRNA synthetase 1-related autosomal recessive hypomyelinating leucodystrophy", "Arginyl-tRNA synthetase 1-related autosomal recessive hypomyelinating leukodystrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypomyelinating leukodystrophy 9", "shortest_name_length": 4}
{"curie": "MONDO:0021486", "names": ["benign ciliary body tumor", "Benign Ciliary Body Tumor", "Benign tumor of ciliary body", "benign ciliary body neoplasm", "benign tumor of ciliary body", "Benign Ciliary Body Neoplasm", "ciliary body benign neoplasm", "Benign Tumor of Ciliary Body", "Benign tumour of ciliary body", "benign neoplasm of ciliary body", "Benign neoplasm of ciliary body", "Benign Neoplasm of Ciliary Body", "benign tumor of the ciliary body", "Benign Tumor of the Ciliary Body", "benign neoplasm of the ciliary body", "Benign Neoplasm of the Ciliary Body", "Benign neoplasm of ciliary body (disorder)", "benign neoplasm of ciliary body (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of ciliary body", "shortest_name_length": 25}
{"curie": "MONDO:0020586", "names": ["Factor V deficiency", "factor V deficiency", "Factor V Deficiency", "FACTOR V DEFICIENCY", "Reduced factor V activity", "Factor V deficiency (disorder)", "Reduced coagulation factor V activity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "factor V deficiency", "shortest_name_length": 19}
{"curie": "UMLS:C0026683", "names": ["mucocele", "Mucocele", "MUCOCELE", "Mucocoele", "mucoceles", "Mucoceles", "mucus cyst", "Mucus Cyst", "Mucus cyst", "Mucous Cyst", "Mucous cyst", "mucous cyst", "Mucinous cyst", "mucinous cyst", "Mucous retention cyst", "mucous retention cyst", "Mucous cyst (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mucocele", "shortest_name_length": 8}
{"curie": "UMLS:C4727397", "names": ["Recurrent Ovarian Mucinous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Ovarian Mucinous Adenocarcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0008097", "names": ["SFM", "JNP", "Sfm syndrome", "SFM SYNDROME", "SFM syndrome", "organoid Nevus", "Organoid nevus", "Sebaceous mole", "Organoid Nevus", "Nevus sebaceous", "Sebaceous nevus", "nevus sebaceous", "sebaceous nevus", "NEVUS SEBACEOUS", "Organoid naevus", "Solomon syndrome", "Sebaceous naevus", "Naevus sebaceous", "Linear sebaceous nevus", "linear sebaceous nevus", "Linear nevus sebaceous", "linear nevus sebaceous", "linear sebaceous Nevus", "Linear Sebaceous Nevus", "Organoid nevus syndrome", "Nevus sebaceus syndrome", "Nevus, Linear Sebaceous", "organoid nevus syndrome", "Sebaceous Nevus, Linear", "nevus sebaceus syndrome", "nevus sebaceus linearis", "linear naevus sebaceous", "skin-eye-brain syndrome", "Linear sebaceous naevus", "Feuerstein-Mims syndrome", "Jadassohn Nevus Sebaceus", "Schimmelpenning syndrome", "Epidermal nevus syndrome", "sebaceous nevus syndrome", "epidermal nevus syndrome", "naevus sebaceus linearis", "nevus sebaceous jadassohn", "Epidermal naevus syndrome", "Jadassohn Sebaceous Nevus", "Nevus sebaceous (disorder)", "Nevus sebaceus of Jadassohn", "organoid nevus phakomatosis", "ORGANOID NEVUS PHAKOMATOSIS", "Nevus Sebaceus of Jadassohn", "sebaceous nevus (diagnosis)", "NEVUS SEBACEUS OF JADASSOHN", "nevus sebaceus of Jadassohn", "organoid Nevus phakomatosis", "Nevus Sebaceous of Jadassohn", "Jadassohn Nevus Phakomatosis", "Naevus sebaceus of Jadassohn", "JADASSOHN NEVUS PHAKOMATOSIS", "Sebaceous Nevus of Jadassohn", "sebaceous nevus of jadassohn", "Jadassohn Nevus phakomatosis", "Jadassohn nevus phakomatosis", "nevus sebaceous of Jadassohn", "nevus sebaceous of jadassohn", "Epidermal hamartoma syndrome", "Nevus sebaceous of Jadassohn", "Nevus, Sebaceous of Jadassohn", "Naevus sebaceous of Jadassohn", "Phakomatosis, Jadassohn Nevus", "Nevus Phakomatosis, Jadassohn", "epidermal nevus syndrome (ENS)", "Linear nevus sebaceus syndrome", "sebaceous nevus syndrome linear", "Linear Sebaceous Nevus Syndrome", "linear nevus sebaceous syndrome", "LINEAR SEBACEOUS NEVUS SYNDROME", "Linear sebaceous nevus sequence", "Solomon-Fretzin-Dewald syndrome", "linear sebaceous nevus syndrome", "linear sebaceous Nevus syndrome", "linear sebaceous nevus sequence", "Sebaceous Nevus Syndrome, Linear", "Linear sebaceous naevus sequence", "sebaceous Nevus syndrome, linear", "SEBACEOUS NEVUS SYNDROME, LINEAR", "linear verrucous epidermal nevus", "EPIDERMAL NEVUS SYNDROME, FORMERLY", "nevus sebaceous of Jadassohn (SNJ)", "Jadassohn nevus phakomatosis (JNP)", "Epidermal Nevus syndrome, formerly", "Epidermal nevus syndrome (disorder)", "Schimmelpeming Feurstein Mims syndrome", "nevus sebaceous of Feuerstein and Mims", "Schimmelpeming Feuerstein Mims syndrome", "Schimmelpenning Feuerstein Mims syndrome", "SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME", "Schimmelpenning-Feuerstein-Mims syndrome", "SCHIMMELPENNING-FEUERSTEIN-MIMS syndrome", "Linear sebaceous nevus sequence (disorder)", "nevus sebaceous of Jadassohn (physical finding)", "Schimmelpenning-Feuerstein-Mims syndrome, somatic mosaic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "linear nevus sebaceous syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0022790", "names": ["cleft tongue", "bifid tongue", "cleft tongue syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleft tongue", "shortest_name_length": 12}
{"curie": "MONDO:0015363", "names": ["autosomal recessive dSMA", "autosomal recessive dHMN", "autosomal recessive distal spinal muscular atrophy", "autosomal recessive distal hereditary motor neuropathy", "distal hereditary motor neuropathy, autosomal recessive", "autosomal recessive distal hereditary motor neuronopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive distal hereditary motor neuropathy", "shortest_name_length": 24}
{"curie": "UMLS:C3714513", "names": ["Unspecified Tissue Injury", "Connective and Soft Tissue Injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Connective and Soft Tissue Injury", "shortest_name_length": 25}
{"curie": "UMLS:C4725772", "names": ["Severe Mosquito Bite Allergy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Severe Mosquito Bite Allergy", "shortest_name_length": 28}
{"curie": "UMLS:C1266064", "names": ["Digital Papillary Adenoma", "Aggressive Digital Papillary Adenoma", "Aggressive digital papillary adenoma", "Aggressive digital papillary adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aggressive digital papillary adenoma", "shortest_name_length": 25}
{"curie": "UMLS:C1335162", "names": ["Ovarian Granulosa-Stromal Tumor", "Ovarian Granulosa-Stromal Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Granulosa-Stromal Cell Tumor", "shortest_name_length": 31}
{"curie": "MONDO:0013642", "names": ["HPE11", "HOLOPROSENCEPHALY 11", "holoprosencephaly 11", "CDON holoprosencephaly", "holoprosencephaly type 11", "holoprosencephaly caused by mutation in CDON"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "holoprosencephaly 11", "shortest_name_length": 5}
{"curie": "MONDO:0700065", "names": ["Trisomy", "trisomy", "Trisomies", "trisomies", "syndrome; trisomy", "Autosomal trisomy", "trisomy; syndrome", "trisomy (diagnosis)", "Autosomal duplication", "accessory; chromosome", "Chromosomal Triplication", "chromosomal triplication", "Chromosomal Triplications", "Trisomy (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trisomy", "shortest_name_length": 7}
{"curie": "MONDO:0024556", "names": ["FFEVF", "FPEVF", "FFEVF1", "epilepsy, partial, with variable foci", "EPILEPSY, PARTIAL, WITH VARIABLE FOCI", "Epilepsy, Partial, with Variable Foci", "Familial focal epilepsy with variable foci", "Familial partial epilepsy with variable foci", "EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI", "epilepsy, familial focal, with variable foci", "Familial Focal Epilepsy with Variable Foci 1", "EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 1", "epilepsy, familial focal, with variable foci 1", "FFEVF - familial focal epilepsy with variable foci", "DEPDC5 epilepsy, familial focal, with variable foci", "Familial focal epilepsy with variable foci (disorder)", "Familial focal epilepsy with variable foci (diagnosis)", "epilepsy, familial focal, with variable foci caused by mutation in DEPDC5", "epilepsy localization-related symptomatic familial focal with variable foci"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, familial focal, with variable foci 1", "shortest_name_length": 5}
{"curie": "MONDO:0033653", "names": ["MC4DN18", "mitochondrial complex 4 deficiency, nuclear type 18", "MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 18", "mitochondrial complex IV deficiency, nuclear type 18"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 4 deficiency, nuclear type 18", "shortest_name_length": 7}
{"curie": "MONDO:0004892", "names": ["ametropia", "Ametropia", "ametropias", "Ametropias", "Error refraction", "ERROR REFRACTION", "error refractive", "error refraction", "Refractive Error", "refractive error", "refraction error", "Refractive error", "REFRACTION ERROR", "REFRACTIVE ERROR", "refraction errors", "Refraction Errors", "Error, Refractive", "errors refractive", "Refractive errors", "refractive errors", "Refraction errors", "errors refraction", "Refractive Errors", "Errors, Refractive", "refractive disorder", "Refraction disorder", "refraction; anomaly", "DISORDER REFRACTION", "anomaly; refraction", "REFRACTION DISORDER", "Refractive Disorder", "Disorder refraction", "Disorder;refraction", "Refractive Disorders", "disorders refraction", "Disorder, Refractive", "refraction; disorder", "disorder; refraction", "refractive disorders", "Refractive error, NOS", "Disorders, Refractive", "Refractive errors NOS", "disorder of refraction", "Disorder of refraction", "Refraction disorder of", "REFRACTION DISORDER OF", "eye refraction disorder", "obsolete_refractive error", "Disorder of refraction, NOS", "refractive error (diagnosis)", "refractive disorders (diagnosis)", "Disorder of refraction (disorder)", "Unspecified disorder of refraction", "Disorder of refraction, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "refractive error", "shortest_name_length": 9}
{"curie": "UMLS:C1336857", "names": ["Undifferentiated Fallopian Tube Cancer", "Fallopian Tube Undifferentiated Carcinoma", "Undifferentiated Fallopian Tube Carcinoma", "Undifferentiated Carcinoma of Fallopian Tube", "undifferentiated carcinoma of fallopian tube", "Undifferentiated Carcinoma of the Fallopian Tube", "undifferentiated carcinoma of fallopian tube (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Undifferentiated Fallopian Tube Carcinoma", "shortest_name_length": 38}
{"curie": "MONDO:0014712", "names": ["SLSN9", "Senior-Loken syndrome 9", "SENIOR-LOKEN SYNDROME 9", "Senior-Loken syndrome type 9", "TRAF3IP1 Senior-Loken syndrome", "Senior-Loken syndrome 9; SLSN9", "Senior-Loken syndrome caused by mutation in TRAF3IP1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Senior-Loken syndrome 9", "shortest_name_length": 5}
{"curie": "UMLS:C1960764", "names": ["Crohn disease in remission", "Crohn's disease in remission", "Crohn's disease in remission (disorder)", "Crohn's disease in remission (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Crohn's disease in remission", "shortest_name_length": 26}
{"curie": "MONDO:0000891", "names": ["mixed fibrolamellar hepatocellular carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed fibrolamellar hepatocellular carcinoma", "shortest_name_length": 44}
{"curie": "UMLS:C0393679", "names": ["Amygdalo-hippocampal epilepsy", "Amygdalo-Hippocampal Epilepsy", "amygdalo-hippocampal epilepsy", "Amygdalo-Hippocampal Epilepsies", "Epilepsies, Amygdalo-Hippocampal", "Amygdalo-hippocampal epilepsy (disorder)", "amygdalo-hippocampal epilepsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Amygdalo-Hippocampal Epilepsy", "shortest_name_length": 29}
{"curie": "UMLS:C4526731", "names": ["Lung Non-Small Cell Cancer by AJCC v7 Stage", "Lung Non-Small Cell Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Non-Small Cell Cancer by AJCC v7 Stage", "shortest_name_length": 43}
{"curie": "MONDO:0001850", "names": ["female breast lower-outer quadrant cancer", "malignant tumor of lower outer quadrant of female breast", "malignant neoplasm of lower-outer quadrant of female breast", "Malignant neoplasm of lower-outer quadrant of female breast", "malignant neoplasm of lower outer quadrant of female breast", "Malignant neoplasm of lower-outer quadrant of breast, female", "Malignant neoplasm of lower-outer quadrant of female breast (disorder)", "malignant neoplasm of lower outer quadrant of female breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "female breast lower-outer quadrant cancer", "shortest_name_length": 41}
{"curie": "UMLS:C0586356", "names": ["Moderate Esophageal Dysplasia", "Moderate esophageal dysplasia", "Moderate oesophageal dysplasia", "Moderate esophageal dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Moderate esophageal dysplasia", "shortest_name_length": 29}
{"curie": "UMLS:C2721727", "names": ["Burkholderia cepacia complex infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Burkholderia cepacia complex infection", "shortest_name_length": 38}
{"curie": "UMLS:C5446388", "names": ["Lacrimal Gland Oncocytic Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lacrimal Gland Oncocytic Adenocarcinoma", "shortest_name_length": 39}
{"curie": "UMLS:C4525307", "names": ["Stage IVB Gallbladder Cancer", "Stage IVB Gallbladder Cancer AJCC v8", "Stage IVB Gallbladder Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Gallbladder Cancer AJCC v8", "shortest_name_length": 28}
{"curie": "UMLS:C5420281", "names": ["Nodal Merkel Cell Carcinoma", "Merkel Cell Carcinoma of Lymph Node", "Extracutaneous Merkel Cell Carcinoma", "Unknown Primary Merkel Cell Carcinoma", "Merkel Cell Carcinoma of Unknown Primary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extracutaneous Merkel Cell Carcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0016656", "names": ["Del(7)(q31)", "monosomy 7q31", "7q31 microdeletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "7q31 microdeletion syndrome", "shortest_name_length": 11}
{"curie": "UMLS:C0278495", "names": ["stage I gastric cancer", "Stomach cancer stage I", "Gastric cancer stage I", "Stage I Gastric Cancer", "gastric cancer, stage I", "stomach cancer, stage I", "Gastric malignancy stage I", "Stage I Gastric Cancer AJCC v7", "Stage I Gastric (Stomach) Cancer", "Malignant neoplasm of stomach stage I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant neoplasm of stomach stage I", "shortest_name_length": 22}
{"curie": "MONDO:0007167", "names": ["AO1", "AOI", "atelosteogenesis type I", "Atelosteogenesis Type I", "Atelosteogenesis type I", "atelosteogenesis type 1", "Atelosteogenesis Type 1", "Atelosteogenesis type 1", "Atelosteogenesis, Type I", "Atelosteogenesis, type 1", "ATELOSTEOGENESIS, TYPE I", "atelosteogenesis, type I", "atelosteogenesis, type 1", "giant cell chondrodysplasia", "GIANT CELL CHONDRODYSPLASIA", "Giant cell chondrodysplasia", "Spondylohumerofemoral hypoplasia", "SPONDYLOHUMEROFEMORAL HYPOPLASIA", "spondylohumerofemoral hypoplasia", "Spondylo-humero-femoral dysplasia", "spondylo-humero-femoral dysplasia", "Atelosteogenesis type 1 (disorder)", "Atelosteogenesis/diastrophic dysplasia group"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atelosteogenesis type I", "shortest_name_length": 3}
{"curie": "UMLS:C0277004", "names": ["Opisthorchis felineus Infection", "Opisthorchis felineus infection", "Opisthorchis felineus Infections", "Infection, Opisthorchis felineus", "Infections, Opisthorchis felineus", "Infection by Opisthorchis felineus", "Opisthorchis felineus opisthorchiasis", "Infection by Opisthorchis tenuicollis", "Infection caused by Opisthorchis felineus", "Infection by Opisthorchis felineus (disorder)", "Opisthorchiasis caused by Opisthorchis felineus", "Infection caused by Opisthorchis felineus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Opisthorchis felineus Infection", "shortest_name_length": 31}
{"curie": "UMLS:C0085511", "names": ["tooth demineralization", "Tooth demineralization", "Tooth demineralisation", "Tooth Demineralization", "Demineralization, Tooth", "Demineralization of tooth", "Demineralisation of tooth", "Hypocalcification of teeth", "Hypocalcification of tooth", "hypocalcification of teeth", "Hypomineralization of tooth", "Hypomineralisation of teeth", "Hypomineralisation of tooth", "Hypomineralization of teeth", "Demineralization of tooth (disorder)", "Hypocalcification of teeth (disorder)", "Hypomineralization of tooth (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tooth Demineralization", "shortest_name_length": 22}
{"curie": "MONDO:0010746", "names": ["Adducted thumb", "Adducted thumbs", "Inward turned thumb", "Thumb-in-palm pattern", "thumb-in-palm deformity", "Thumb in palm deformity", "Thumb-in-palm deformity", "Congenital clasped thumb", "adducted thumbs syndrome", "Adducted Thumbs Syndrome", "ADDUCTED THUMBS SYNDROME", "thumbs, congenital Clasped", "Thumbs, Congenital Clasped", "Clasped thumbs, congenital", "THUMBS, CONGENITAL CLASPED", "ADDUCTED THUMBS, CONGENITAL", "Thumb in palm deformity (disorder)", "thumb-in-palm deformity was observed", "thumb-in-palm deformity (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thumbs, congenital Clasped", "shortest_name_length": 14}
{"curie": "UMLS:C5447671", "names": ["EWSR1-SMAD3-Positive Fibroblastic Tumor", "EWSR1::SMAD3-Positive Fibroblastic Tumor", "EWSR1-SMAD3-Rearranged Fibroblastic Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "EWSR1-SMAD3-Positive Fibroblastic Tumor", "shortest_name_length": 39}
{"curie": "UMLS:C2882221", "names": ["Acute pulmonary embolism", "pulmonary embolism acute", "Acute Pulmonary Embolism", "Acute pulmonary embolism NOS", "Acute pulmonary embolism (disorder)", "Acute pulmonary embolism (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute pulmonary embolism", "shortest_name_length": 24}
{"curie": "UMLS:C4521742", "names": ["Stage II Esophageal Squamous Cell Cancer", "Pathologic Stage II Esophageal Squamous Cell Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage II Esophageal Squamous Cell Carcinoma AJCC v8", "shortest_name_length": 40}
{"curie": "MONDO:0033135", "names": ["CMT1G", "PMP2-related CMT1", "Charcot-Marie-Tooth disease type 1G", "PMP2-related Charcot-Marie-Tooth disease type 1", "PMP2-related Charcot-Marie-Tooth neuropathy type 1", "Charcot-Marie-Tooth disease, demyelinating, type 1G", "CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1G", "PMP2-related hereditary motor and sensory neuropathy type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease, demyelinating, type 1G", "shortest_name_length": 5}
{"curie": "UMLS:C0281710", "names": ["Large Cell Lymphoma", "Pediatric Large Cell Lymphoma", "childhood large cell lymphoma", "Childhood Large Cell Lymphoma", "pediatric large cell lymphoma", "lymphoma, childhood large cell", "large cell lymphoma, childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Large Cell Lymphoma", "shortest_name_length": 19}
{"curie": "UMLS:C0334445", "names": ["Type A Spindle Cell Melanoma", "melanoma; spindle cell type A", "Spindle cell melanoma, type A", "Spindle cell melanoma - type A", "spindle cell; melanoma, type A", "Spindle Cell Type A Malignant Melanoma", "Malignant Spindle Cell Type A Melanoma", "Spindle cell melanoma, type A (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spindle cell melanoma, type A", "shortest_name_length": 28}
{"curie": "UMLS:C5419086", "names": ["Advanced Pancreatobiliary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Pancreatobiliary Carcinoma", "shortest_name_length": 35}
{"curie": "MONDO:0000087", "names": ["Microgyria", "microgyria", "polymicrogyria", "Polymicrogyria", "Micropolygyria", "Micropolygyrias", "Polymicrogyrias", "More grooves in brain", "Microgyria (disorder)", "microgyria (diagnosis)", "Cerebral Polymicrogyria", "Cerebral Micropolygyria", "Cerebral Micropolygyrias", "Cerebral Polymicrogyrias", "Micropolygyria, Cerebral", "Polymicrogyria, Cerebral", "Micropolygyrias, Cerebral", "Polymicrogyrias, Cerebral", "polymicrogyria (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polymicrogyria", "shortest_name_length": 10}
{"curie": "MONDO:0021634", "names": ["epithelial skin tumor", "skin epithelium tumor", "Skin Epithelium Tumor", "Epithelial Skin Tumor", "skin epithelium neoplasm", "Epithelial Skin Neoplasm", "Skin Epithelium Neoplasm", "epithelial skin neoplasm", "Tumor of surface epithelium", "Epithelial neoplasm of skin", "Tumour of surface epithelium", "zone of skin epithelial neoplasm", "Epithelial neoplasm of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epithelial skin neoplasm", "shortest_name_length": 21}
{"curie": "MONDO:0020850", "names": ["MRT65", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 65", "mental retardation, autosomal recessive 65", "intellectual disability, autosomal recessive 65", "autosomal recessive intellectual developmental disorder 65", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 65"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 65", "shortest_name_length": 5}
{"curie": "MONDO:0017283", "names": ["Del(10)(p11.21p12.31)", "deletion 10p11.21p12.31", "monosomy 10p11.21p12.31", "10p12p11 microdeletion syndrome", "DeSanto-Shinawi Syndrome due to 10p11.21p12.31 microdeletion", "facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DeSanto-Shinawi Syndrome due to 10p11.21p12.31 microdeletion", "shortest_name_length": 21}
{"curie": "MONDO:0001050", "names": ["otitis externa malignant", "Malignant otitis externa", "externa malignant otitis", "malignant otitis externa", "OTITIS EXTERNA, MALIGNANT", "Necrotizing otitis externa", "otitis; externa, malignant", "Necrotising otitis externa", "Malignant otitis externa (disorder)", "malignant otitis externa (diagnosis)", "otitis; externa, Pseudomonas aeruginosa", "Malignant otitis externa, unspecified ear", "Otitis externa due to Pseudomonas aeruginosa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant otitis externa", "shortest_name_length": 24}
{"curie": "MONDO:0011228", "names": ["CREASES, INFRA-AURICULAR CUTANEOUS, WITH TALL STATURE AND ADVANCED BONE AGE", "creases, infra-auricular cutaneous, with tall stature and advanced bone age", "Creases, Infra-Auricular Cutaneous, with Tall Stature and Advanced Bone Age"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "creases, infra-auricular cutaneous, with tall stature and advanced bone age", "shortest_name_length": 75}
{"curie": "MONDO:0014643", "names": ["BVSYS", "Basel-Vanagait-Smirin-Yosef syndrome", "Basel-Vanagaite-Smirin-Yosef syndrome", "BASEL-Vanagaite-SMIRIN-YOSEF syndrome", "Basel Vanagaite Smirin Yosef syndrome", "BASEL-VANAGAITE-SMIRIN-YOSEF SYNDROME", "Basel Vanagaite Smirin Yosef syndrome (disorder)", "congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0017711", "names": ["pancreatic colipase deficiency", "Pancreatic colipase deficiency", "PANCREATIC COLIPASE DEFICIENCY", "Pancreatic colipase deficiency (disorder)", "pancreatic colipase deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic colipase deficiency", "shortest_name_length": 30}
{"curie": "UMLS:C0151898", "names": ["REACTION SCHIZOID", "Reaction schizoid", "SCHIZOPHRENIC REACTION", "schizophrenic reaction", "Schizophrenic reaction", "schizophrenic; reaction", "reaction; schizophrenic", "schizophrenia; reaction", "Schizophrenic reaction NOS", "Schizophrenic reaction, NOS", "Schizophrenic reaction (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Schizophrenic reaction", "shortest_name_length": 17}
{"curie": "UMLS:C1708901", "names": ["Malignant Accessory Urethral Gland Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Accessory Urethral Gland Neoplasm", "shortest_name_length": 43}
{"curie": "MONDO:0005114", "names": ["Pneumococcal Disease", "Pneumococcal disease", "Pneumococcal Diseases", "Disease, Pneumococcal", "Pneumococcal Infection", "Diseases, Pneumococcal", "Pneumococcal infection", "pneumococcal infection", "Pneumococcus; infection", "Infection, Pneumococcal", "pneumococcal infections", "PNEUMOCOCCAL INFECTIONS", "Pneumococcal Infections", "infection; pneumococcus", "infection, pneumococcal", "Infections, Pneumococcal", "infections, pneumococcal", "Pneumococcal infection NOS", "Pneumococcal infection, NOS", "Pneumococcal infectious disease", "Streptococcus pneumoniae infection", "Streptococcus pneumoniae Infection", "Infection, Streptococcus pneumoniae", "Streptococcus pneumoniae infections", "Streptococcus Pneumoniae Infections", "pneumoniae infection, Streptococcus", "infection, Streptococcus pneumoniae", "Streptococcus pneumoniae Infections", "Pneumococcal infectious disease, NOS", "pneumoniae infections, Streptococcus", "Infections, Streptococcus pneumoniae", "infections, Streptococcus pneumoniae", "Pneumococcal infectious disease (disorder)", "Streptococcus pneumoniae infectious disease", "Streptococcus pneumoniae disease or disorder", "Streptococcus pneumoniae infection (diagnosis)", "Streptococcus pneumoniae caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pneumococcal infection", "shortest_name_length": 20}
{"curie": "UMLS:C0156690", "names": ["Unspecified postpartum hypertension", "Unspecified Postpartum Hypertension", "Unspecified hypertension complicating pregnancy, childbirth, or the puerperium, postpartum condition or complication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unspecified postpartum hypertension", "shortest_name_length": 35}
{"curie": "UMLS:C2748208", "names": ["EFD", "Executive dysfunction", "Executive Dysfunction", "Executive Function Disorder", "Executive function disorder", "Executive Functioning Deficit", "Impairment of Executive Functions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Executive dysfunction", "shortest_name_length": 3}
{"curie": "MONDO:0008353", "names": ["PUPPP", "papular dermatitis pregnancy", "eruption polymorphic pregnancy", "papular dermatitis of pregnancy", "Papular dermatitis of pregnancy", "polymorphic eruption of pregnancy", "POLYMORPHIC ERUPTION OF PREGNANCY", "Polymorphic eruption of pregnancy", "PEP - Polymorphic eruption of pregnancy", "PEP - polymorphic eruption of pregnancy", "Polymorphic eruption of pregnancy (disorder)", "PRURITIC URTICARIAL PAPULES PLAQUE PREGNANCY", "Pruritic urticarial papules plaques of pregnancy", "pruritic urticarial papules plaques of pregnancy", "Pruritic Urticarial Papules And Plaques of Pregnancy", "PRURITIC URTICARIAL PAPULES AND PLAQUES OF PREGNANCY", "Pruritic urticarial papules and plaques of pregnancy", "pruritic urticarial papules and plaques of pregnancy", "PUPPP Pruritic urticarial papules plaques of pregnancy", "PUPPP - pruritic urticarial papules and plaques of pregnancy", "Pruritic urticarial papules and plaques of pregnancy (PUPPP)", "PUPPP - Pruritic urticarial papules and plaques of pregnancy", "pruritic urticarial papules and plaques of pregnancy (PUPPP)", "pruritic urticarial papules and plaques of pregnancy, familial (subtype)", "pruritic urticarial papules and plaques of pregnancy (PUPPP) (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pruritic urticarial papules and plaques of pregnancy", "shortest_name_length": 5}
{"curie": "MONDO:0020723", "names": ["VDDI", "VDD1", "PDDRI", "VDDRI", "PDDR1A", "VDDR1A", "VDDR-I", "PDDR IA", "PDDR 1A", "Pseudodeficiency rickets", "Vitamin D-dependency type I", "Vitamin D Dependency, Type 1", "vitamin D dependency, type 1", "VITAMIN D DEPENDENCY, TYPE 1", "1-alpha-hydroxylase deficiency", "1-Alpha-Hydroxylase deficiency", "1-ALPHA-HYDROXYLASE DEFICIENCY", "1-Alpha-Hydroxylase Deficiency", "Calcidiol 1-monooxygenase defect", "Pseudovitamin D-deficient rickets", "Pseudovitamin D-resistant rickets", "Pseudovitamin D deficiency rickets", "Vitamin D-dependent rickets type I", "Pseudo-vitamin D resistant rickets", "Vitamin D dependent rickets type I", "Vitamin D-Dependent Rickets Type 1", "Pseudo-vitamin-D-deficient rickets", "type I vitamin D dependent rickets", "vitamin D-dependent rickets type 1A", "vitamin D-dependent rickets, type I", "Vitamin D-dependent rickets, type 1", "VITAMIN D-DEPENDENT RICKETS, TYPE 1A", "Vitamin D-Dependent Rickets, Type 1A", "vitamin D-dependent rickets, type 1A", "Vitamin D 1 Alpha-Hydroxylase Deficiency", "Hypocalcemic vitamin D-dependent rickets", "PDDR - Pseudovitamin D deficiency rickets", "Pseudovitamin D-Deficiency Rickets, Type IA", "PSEUDOVITAMIN D-DEFICIENCY RICKETS, TYPE IA", "VDDR I - Vitamin D-dependent rickets type I", "pseudovitamin D-deficiency rickets, type 1A", "type I vitamin D dependent rickets (diagnosis)", "Vitamin D-dependent rickets, type 1 (disorder)", "25-Hydroxycholecalciferol-1-hydroxylase deficiency", "VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A", "Vitamin D Hydroxylation-Deficient Rickets, Type 1A", "25-hydroxycholecalciferol-1-Hydroxylase deficiency", "vitamin D hydroxylation-deficient rickets, type 1A", "25-HYDROXYCHOLECALCIFEROL-1-HYDROXYLASE DEFICIENCY", "25-Hydroxycholecalciferol-1-Hydroxylase Deficiency", "1-Alpha, 25-Hydroxyvitamin D3 deficiency, selective", "1-Alpha, 25-Hydroxyvitamin D3 Deficiency, Selective", "1-ALPHA, 25-HYDROXYVITAMIN D3 DEFICIENCY, SELECTIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitamin D-dependent rickets, type 1A", "shortest_name_length": 4}
{"curie": "UMLS:C1336124", "names": ["Stage IA Small Cell Lung Cancer", "Stage IA Small Cell Lung Carcinoma", "Stage IA Small Cell Carcinoma of Lung", "Stage IA Small Cell Carcinoma of the Lung", "Stage IA Lung Small Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Lung Small Cell Carcinoma AJCC v7", "shortest_name_length": 31}
{"curie": "MONDO:0010939", "names": ["LPAC", "GBD1", "GALLBLADDER DISEASE 1", "gallbladder disease 1", "gallbladder disease type 1", "ABCB4-related cholelithiasis", "cholelithiasis with ABCB4 gene mutation", "Cholelithiasis with ABCB4 gene mutation", "Low phospholipid-associated cholelithiasis", "low phospholipid associated cholelithiasis", "Low phospholipid associated cholelithiasis", "CHOLELITHIASIS, LOW PHOSPHOLIPID-ASSOCIATED", "cholelithiasis, Low phospholipid-associated", "ABCB4 gene mutation-associated cholelithiasis", "Low phospholipid associated cholelithiasis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "low phospholipid associated cholelithiasis", "shortest_name_length": 4}
{"curie": "MONDO:0013121", "names": ["GLC3C", "glaucoma 3, primary congenital, C"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glaucoma 3, primary congenital, C", "shortest_name_length": 5}
{"curie": "MONDO:0016743", "names": ["Meninges Tumor", "meninges tumor", "tumor meninges", "Meningeal tumor", "meningeal tumor", "Meningeal Tumor", "Meningeal Tumors", "Meningeal tumour", "Tumor, Meningeal", "Meninges Neoplasm", "Tumor of meninges", "tumor of meninges", "Tumor of Meninges", "meninges neoplasm", "Tumors, Meningeal", "Tumour of meninges", "Meningeal neoplasm", "Meningeal Neoplasm", "meningeal neoplasm", "Meningeal Neoplasms", "meningeal neoplasms", "Neoplasm, Meningeal", "Neoplasm of Meninges", "meningothelial tumor", "Neoplasm of meninges", "neoplasm of meninges", "Neoplasms, Meningeal", "tumor of the meninges", "Tumor of the Meninges", "Meningeal neoplasm NOS", "meningeal cluster tumor", "Meningeal-derived tumor", "Meningeal-derived tumors", "neoplasm of the meninges", "Neoplasm of the Meninges", "Meningeal-derived tumour", "Meningeal-derived tumours", "meningeal cluster neoplasm", "tumor of meningeal cluster", "neoplasm of meningeal cluster", "Meningeal neoplasm (morphology)", "Neoplasm of meninges (disorder)", "neoplasm of meninges (diagnosis)", "meningeal cluster neoplasm (disease)", "meningeal cluster rare nervous system tumor", "Meningeal neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tumor of meninges", "shortest_name_length": 14}
{"curie": "MONDO:0013178", "names": ["MDCL", "Mdcl", "L-CMD", "muscular dystrophy, congenital", "LMNA congenital muscular dystrophy", "LMNA-related congenital muscular dystrophy", "congenital muscular dystrophy LMNA-related", "Muscular Dystrophy Congenital, LMNA-Related", "muscular dystrophy Congenital, LMNA-related", "MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED", "Muscular Dystrophy, Congenital, Lmna-Related", "muscular dystrophy, congenital, LMNA-related", "congenital muscular dystrophy due to LMNA mutation", "Congenital muscular dystrophy due to LMNA mutation", "MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED (disorder)", "Congenital muscular dystrophy due to lamin A/C mutation", "congenital muscular dystrophy caused by mutation in LMNA", "Congenital muscular dystrophy due to LMNA (lamin A/C) mutation", "Congenital muscular dystrophy due to lamin A/C mutation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital muscular dystrophy due to LMNA mutation", "shortest_name_length": 4}
{"curie": "MONDO:0003301", "names": ["Dartoic myoma", "Dartoic Myoma", "dartoic myoma", "Dartoic leiomyoma", "Dartoic Leiomyoma", "dartoic leiomyoma", "dartos muscle leiomyoma", "Dartoic myoma (disorder)", "leiomyoma of dartos muscle"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dartoic leiomyoma", "shortest_name_length": 13}
{"curie": "UMLS:C1328330", "names": ["Biliary anastomosis complication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Biliary anastomosis complication", "shortest_name_length": 32}
{"curie": "MONDO:0001653", "names": ["prepuce cancer", "cancer of prepuce", "Cancer of foreskin", "PREPUCE MALIGNANT NEOPLASM", "malignant prepuce neoplasm", "Malignant tumor of prepuce", "Malignant tumour of prepuce", "malignant tumor of foreskin", "Malignant tumor of foreskin", "Malignant tumour of foreskin", "Malignant neoplasm of prepuce", "malignant neoplasm of prepuce", "malignant neoplasm of foreskin", "Malignant neoplasm of foreskin", "penile neoplasm malignant prepuce", "Malignant tumor of foreskin (disorder)", "Malignant neoplasm of prepuce (foreskin)", "malignant neoplasm of prepuce (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prepuce cancer", "shortest_name_length": 14}
{"curie": "UMLS:C0280144", "names": ["Stage II Grade 2 Follicular Lymphoma", "stage II grade 2 follicular lymphoma", "Grade II Follicular Lymphoma Stage II", "Stage II Grade II Follicular Lymphoma", "Follicular Mixed Cell Lymphoma Stage II", "Stage II Follicular Mixed Cell Lymphoma", "stage II follicular mixed cell lymphoma", "follicular mixed cell lymphoma, stage II", "Ann Arbor Stage II Grade 2 Follicular Lymphoma", "Grade II Follicular Mixed Cell Lymphoma Stage II", "stage II grade II follicular mixed cell lymphoma", "Stage II Grade II Follicular Mixed Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage II Grade 2 Follicular Lymphoma", "shortest_name_length": 36}
{"curie": "UMLS:C0023904", "names": ["Experimental Liver Neoplasm", "Liver Neoplasm, Experimental", "Experimental Liver Neoplasms", "Liver Neoplasms, Experimental", "Neoplasms, Experimental Liver"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liver Neoplasms, Experimental", "shortest_name_length": 27}
{"curie": "MONDO:0005991", "names": ["His-Werner", "Trench Fever", "FEVER, MEUSE", "TRENCH FEVER", "Trench fever", "trench fever", "trench fevers", "quintan fever", "fever; trench", "trench; fever", "Quintan fever", "fever, trench", "Fever, Trench", "FEVER, QUINTAN", "quintan; fever", "fevers, trench", "fever; quintan", "Five day fever", "five day fever", "wolhynian fever", "FEVER, FIVE-DAY", "shin bone fever", "Wolhynian fever", "Febris quintata", "tibialgic fever", "fever; wolhynian", "FEVER, SHIN BONE", "FEVER, VOLHYNIAN", "quintana; febris", "febris; quintana", "wolhynian; fever", "His-Werner disease", "HIS-WERNER DISEASE", "fever; trench fever", "trench fever; fever", "Trench fever (disorder)", "trench fever (diagnosis)", "Bartonella quintana Infection", "Bartonella quintana Infections", "Infection, Bartonella quintana", "Rochalimaea quintana infection", "Fever due to Bartonella quintana", "fever due to Bartonella quintana", "Fever due to Rochalimaea quintana", "trench fever (rickettsia quintana)", "Bartonella quintana infectious disease", "Bartonella quintana disease or disorder", "Bartonella quintana caused disease or disorder", "bartonellosis due to Bartonella quintana infection", "Bartonellosis due to Bartonella quintana infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trench fever", "shortest_name_length": 10}
{"curie": "UMLS:C0206068", "names": ["Parasystole", "parasystole", "PARASYSTOLIA", "Parasystoles", "Parasystolia", "Parasystole, NOS", "Parasystolic beat", "Parasystolic beat, NOS", "Parasystole (disorder)", "parasystole (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parasystole", "shortest_name_length": 11}
{"curie": "MONDO:0014831", "names": ["MFLS", "MARFANOID-PROGEROID SYNDROME", "Marfanoid-progeroid syndrome", "Marfan lipodystrophy syndrome", "MARFAN LIPODYSTROPHY SYNDROME", "Marfan-progeroid-lipodystrophy syndrome", "MARFAN-PROGEROID-LIPODYSTROPHY SYNDROME", "MARFANOID-PROGEROID-LIPODYSTROPHY SYNDROME", "progeroid and marfanoid aspect-lipodystrophy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progeroid and marfanoid aspect-lipodystrophy syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0000913", "names": ["HS2", "SPH2", "spherocytosis, type 2", "SPHEROCYTOSIS, TYPE 2", "hereditary spherocytosis 2", "SPHEROCYTOSIS, HEREDITARY, 2", "spherocytosis, hereditary, 2", "SPTB hereditary spherocytosis", "hereditary spherocytosis type 2", "hereditary spherocytosis caused by mutation in SPTB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spherocytosis type 2", "shortest_name_length": 3}
{"curie": "MONDO:0008875", "names": ["Frydman-Cohen-Karmon syndrome", "Frydman Cohen Karmon syndrome", "Blepharophimosis with ptosis, syndactyly, and short stature", "BLEPHAROPHIMOSIS WITH PTOSIS, SYNDACTYLY, AND SHORT STATURE", "blepharophimosis with ptosis, syndactyly, and short stature", "blepharophimosis - ptosis - esotropia - syndactyly - short stature", "Blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome", "blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome", "Blepharophimosis, ptosis, esotropia, syndactyly, short stature syndrome", "Blepharophimosis, ptosis, esotropia, syndactyly, short stature syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome", "shortest_name_length": 29}
{"curie": "MONDO:0007433", "names": ["Dementia-Parkinsonism With Non-Alzheimer Amyloid Plaques", "DEMENTIA/PARKINSONISM WITH NON-ALZHEIMER AMYLOID PLAQUES", "dementia/parkinsonism with non-Alzheimer amyloid plaques"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dementia/parkinsonism with non-Alzheimer amyloid plaques", "shortest_name_length": 56}
{"curie": "MONDO:0006890", "names": ["parathyroid adenoma", "PARATHYROID ADENOMA", "adenoma parathyroid", "Parathyroid Adenoma", "Parathyroid adenoma", "Parathyroid Adenomas", "Adenoma, Parathyroid", "adenomas parathyroid", "Parathyroid adenomas", "Adenomas, Parathyroid", "adenoma of parathyroid", "parathyroid gland adenoma", "Parathyroid Gland Adenoma", "adenoma of the parathyroid", "adenoma of parathyroid gland", "Parathyroid adenoma (disorder)", "adenoma of the Parathyroid gland", "adenoma of the parathyroid gland", "ADENOMA, PARATHYROID GLAND, BENIGN", "adenoma of parathyroid gland (diagnosis)", "primary hyperparathyroidism due to adenoma", "primary hyperparathyroidism due to adenoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parathyroid gland adenoma", "shortest_name_length": 19}
{"curie": "UMLS:C2931356", "names": ["Spastic paraplegia type 5A, recessive", "Autosomal recessive spastic paraplegia", "autosomal recessive spastic paraplegia", "familial spastic paraplegia autosomal recessive", "autosomal recessive spastic paraplegia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spastic paraplegia type 5A, recessive", "shortest_name_length": 37}
{"curie": "MONDO:0000898", "names": ["malignant hemangioma", "Malignant hemangioma", "hemangioma, malignant", "Malignant haemangioma", "Malignant hemangioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant hemangioma", "shortest_name_length": 20}
{"curie": "UMLS:C0278712", "names": ["stage II Wilms tumor", "Stage II Wilms Tumor", "Wilms tumor, stage II", "stage II Wilm's tumor", "stage II Wilms' tumor", "Wilms' tumor, stage II", "Wilm's tumor, stage II", "stage II nephroblastoma", "nephroblastoma, stage II", "Stage II Renal Wilms Tumor", "Stage II Kidney Wilms Tumor", "Stage II Renal Wilms' Tumor", "Stage II Kidney Nephroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Kidney Wilms Tumor", "shortest_name_length": 20}
{"curie": "MONDO:0001459", "names": ["radial neuropathy", "RADIAL NEUROPATHY", "Radial neuropathy", "Radial Neuropathy", "Neuropathy, Radial", "Supinator Syndrome", "Syndrome, Supinator", "Supinator Syndromes", "Radial Neuropathies", "Radial Nerve Disease", "Radial Nerve Diseases", "Radial Mononeuropathy", "Mononeuropathy, Radial", "Radial Mononeuropathies", "Radial neuropathy (disorder)", "radial nerve peripheral neuropathy", "peripheral neuropathy of radial nerve"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radial neuropathy", "shortest_name_length": 17}
{"curie": "UMLS:C4745272", "names": ["Locally Advanced Pancreatic Ductal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Pancreatic Ductal Adenocarcinoma", "shortest_name_length": 49}
{"curie": "UMLS:C1516434", "names": ["Cervical Squamous Tumor", "Cervical Squamous Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Squamous Neoplasm", "shortest_name_length": 23}
{"curie": "MONDO:0700133", "names": ["adenoma, non-human"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenoma, non-human", "shortest_name_length": 18}
{"curie": "UMLS:C1336811", "names": ["Transplant-Related Hepatocellular Cancer", "Transplant-Related Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transplant-Related Hepatocellular Carcinoma", "shortest_name_length": 40}
{"curie": "UMLS:C0276647", "names": ["Fungal Pericarditis", "Pericarditis fungal", "Fungal pericarditis", "Mycotic pericarditis", "Fungal pericarditis, NOS", "Mycotic pericarditis, NOS", "Mycotic pericarditis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mycotic pericarditis", "shortest_name_length": 19}
{"curie": "MONDO:0001995", "names": ["Sphenoid Sinus Epidermoid Carcinoma", "sphenoid sinus epidermoid carcinoma", "Sphenoidal Sinus Epidermoid Carcinoma", "sphenoidal sinus epidermoid carcinoma", "Epidermoid Carcinoma of Sphenoid Sinus", "Sphenoid Sinus Squamous Cell Carcinoma", "sphenoid sinus squamous cell carcinoma", "epidermoid carcinoma of sphenoid sinus", "Epidermoid Carcinoma of Sphenoidal Sinus", "Sphenoidal Sinus Squamous Cell Carcinoma", "sphenoidal sinus squamous cell carcinoma", "epidermoid carcinoma of sphenoidal sinus", "Squamous Cell Carcinoma of Sphenoid Sinus", "squamous cell carcinoma of sphenoid sinus", "Epidermoid Carcinoma of the Sphenoid Sinus", "epidermoid carcinoma of the sphenoid sinus", "squamous cell carcinoma of sphenoidal sinus", "Squamous cell carcinoma of sphenoidal sinus", "Squamous Cell Carcinoma of Sphenoidal Sinus", "Epidermoid carcinoma of the Sphenoidal sinus", "Epidermoid Carcinoma of the Sphenoidal Sinus", "epidermoid carcinoma of the sphenoidal sinus", "squamous cell carcinoma of the sphenoid sinus", "Squamous Cell Carcinoma of the Sphenoid Sinus", "squamous cell carcinoma of the sphenoidal sinus", "Squamous Cell Carcinoma of the Sphenoidal Sinus", "Primary squamous cell carcinoma of sphenoidal sinus", "Squamous cell carcinoma of sphenoidal sinus (disorder)", "Squamous cell carcinoma of sphenoidal sinus (diagnosis)", "Primary squamous cell carcinoma of sphenoidal sinus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sphenoid sinus squamous cell carcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C0205865", "names": ["OA", "Odontoblastoma", "Odontoameloblastoma", "odontoameloblastoma", "Ameloblastic odontoma", "Ameloblastic Odontoma", "ameloblastic; odontoma", "odontoma; ameloblastic", "Ameloblastic Fibroodontoma", "Fibroameloblastic Odontoma", "Fibroameloblastic odontoma", "odontoma; fibroameloblastic", "fibroameloblastic; odontoma", "Ameloblastic Fibro-Odontoma", "Ameloblastic Fibro-odontoma", "Ameloblastic fibro-odontoma", "Ameloblastic Fibro-odontomas", "Fibro odontoma, Ameloblastic", "fibro-odontoma; ameloblastic", "Fibro-odontoma, Ameloblastic", "Fibro-odontomas, Ameloblastic", "ODONTOMA, AMELOBLASTIC, BENIGN", "Odontoameloblastoma (morphologic abnormality)", "Ameloblastic fibro-odontoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fibro-odontoma, Ameloblastic", "shortest_name_length": 2}
{"curie": "MONDO:0012558", "names": ["Epiphyseal Dysplasia, Baumann Type", "epiphyseal dysplasia, Baumann type", "EPIPHYSEAL DYSPLASIA, BAUMANN TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epiphyseal dysplasia, Baumann type", "shortest_name_length": 34}
{"curie": "UMLS:C3888552", "names": ["Autoimmune colitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Autoimmune colitis", "shortest_name_length": 18}
{"curie": "MONDO:0012202", "names": ["Mals", "MALS", "susceptibility to mild malaria", "malaria, mild, susceptibility to", "MALARIA, MILD, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malaria, mild, susceptibility to", "shortest_name_length": 4}
{"curie": "MONDO:0003305", "names": ["cellular neurofibroma", "Cellular Neurofibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cellular neurofibroma", "shortest_name_length": 21}
{"curie": "UMLS:C1261358", "names": ["Giant Cell Sarcoma", "Giant cell sarcoma", "giant cell sarcoma", "Pleomorphic cell sarcoma", "giant cell sarcoma (diagnosis)", "Undifferentiated pleomorphic cell sarcoma", "Giant cell sarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Giant cell sarcoma", "shortest_name_length": 18}
{"curie": "MONDO:0013412", "names": ["CMH9", "hypertrophic cardiomyopathy 9", "TTN hypertrophic cardiomyopathy", "hypertrophic cardiomyopathy type 9", "Cardiomyopathy, Familial Hypertrophic, 9", "CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9", "cardiomyopathy, familial hypertrophic, 9", "cardiomyopathy, familial hypertrophic, type 9", "hypertrophic cardiomyopathy caused by mutation in TTN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophic cardiomyopathy 9", "shortest_name_length": 4}
{"curie": "MONDO:0016344", "names": ["Hydrancephaly", "hydranencephaly", "Hydranencephaly", "Hydroanencephaly", "Hydranencephalies", "hydranencephaly (disease)", "Hydranencephaly (disorder)", "hydranencephaly (diagnosis)", "Cerebral Hemispheres, Absence, Congenital", "Congenital Absence of Cerebral Hemispheres", "Congenital absence of cerebral hemispheres", "Absence of Cerebral Hemispheres, Congenital"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hydranencephaly", "shortest_name_length": 13}
{"curie": "UMLS:C1698510", "names": ["Bacterial otitis media", "bacterial otitis media", "Otitis media bacterial", "Bacterial otitis media (disorder)", "bacterial otitis media (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bacterial otitis media", "shortest_name_length": 22}
{"curie": "UMLS:C1963776", "names": ["Perihepatic Abscess", "Perihepatic abscess"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perihepatic abscess", "shortest_name_length": 19}
{"curie": "MONDO:0020780", "names": ["CRDHL2", "cone-rod dystrophy and hearing loss 2", "CONE-ROD DYSTROPHY AND HEARING LOSS 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cone-rod dystrophy and hearing loss 2", "shortest_name_length": 6}
{"curie": "MONDO:0021331", "names": ["Parotid Carcinoma", "parotid carcinoma", "carcinoma parotid", "Carcinoma;parotid", "Carcinoma of Parotid", "parotid gland cancer", "Parotid Gland Cancer", "carcinoma of parotid", "parotid gland carcinoma", "Parotid Gland Carcinoma", "carcinoma gland parotid", "carcinoma of the parotid", "Carcinoma of the Parotid", "Carcinoma of parotid gland", "carcinoma of parotid gland", "Carcinoma of Parotid Gland", "Carcinoma of the Parotid Gland", "carcinoma of the parotid gland", "malignant parotid neoplasm carcinoma", "Carcinoma of parotid gland (disorder)", "Carcinoma of parotid gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma of parotid gland", "shortest_name_length": 17}
{"curie": "MONDO:0100129", "names": ["intracranial arachoid cyst", "intracranial arachnoid cyst", "Intracranial Arachnoid Cyst", "arachnoid intracranial cyst", "Intracranial Arachnoid Cysts", "Cyst, Intracranial Arachnoid", "intracranial arachnoid cysts", "Arachnoid Cyst, Intracranial", "Cysts, Intracranial Arachnoid", "ARACHNOID CYSTS, INTRACRANIAL", "Arachnoid Cysts, Intracranial", "arachnoid cysts, intracranial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intracranial arachoid cyst", "shortest_name_length": 26}
{"curie": "MONDO:0005751", "names": ["Bornholm", "DEVIL GRIP", "devil grip", "DABNEY GRIP", "devils grip", "devil's grip", "grip; Dabney", "Devil's grip", "Dabney; grip", "Dabney's grip", "grip; devil's", "devil's; grip", "Bamble disease", "Epidemic myalgia", "BORNHOLM DISEASE", "Epidemic Myalgia", "Bornholm Disease", "epidemic myalgia", "bornholm disease", "SYLVEST SYNDROME", "Bornholm disease", "Bornholms disease", "epidemic pleurisy", "Myalgia, Epidemic", "Bornholm; disease", "MYALGIA, EPIDEMIC", "Epidemic myositis", "Disease;Bornholms", "Epidemic Myalgias", "myalgia; epidemic", "Epidemic pleurisy", "bornholms disease", "epidemic myositis", "Epidemic, myalgia", "epidemic; myalgia", "Myositis;epidemic", "epidemic, myositis", "epidemic; myositis", "Epidemic, myositis", "myositis; epidemic", "Myalgias, Epidemic", "Epidemic Pleurodynia", "epidemic pleurodynia", "Epidemic pleurodynia", "epidemic; pleurodynia", "Pleurodynia, Epidemic", "PLEURODYNIA, EPIDEMIC", "Epidemic Pleurodynias", "pleurodynia; epidemic", "Pleurodynias, Epidemic", "Epidemic benign dry pleurisy", "disease (or disorder); Bornholm", "Epidemic pleurodynia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidemic pleurodynia", "shortest_name_length": 8}
{"curie": "MONDO:0007274", "names": ["carpal bossing", "CARPAL BOSSING", "Carpal bossing", "carpal displacement", "CARPAL DISPLACEMENT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carpal displacement", "shortest_name_length": 14}
{"curie": "UMLS:C4763820", "names": ["Renal Synovial Sarcoma", "Kidney Synovial Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kidney Synovial Sarcoma", "shortest_name_length": 22}
{"curie": "UMLS:C1396651", "names": ["ankle deformity", "Ankle deformity", "ankle; deformity", "deformity; ankle", "Ankle deformities", "deformity of ankle", "deformity of ankle (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ankle deformity", "shortest_name_length": 15}
{"curie": "MONDO:0022812", "names": ["Complement receptor deficiency", "complement receptor deficiency", "Complement receptor deficiency (disorder)", "complement receptor deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complement receptor deficiency", "shortest_name_length": 30}
{"curie": "MONDO:0012794", "names": ["anes", "ANES", "ANE Syndrome", "ANE SYNDROME", "ANE syndrome", "alopecia, neurologic defects, and endocrinopathy syndrome", "Alopecia, Neurologic Defects, and Endocrinopathy Syndrome", "ALOPECIA, NEUROLOGIC DEFECTS, AND ENDOCRINOPATHY SYNDROME", "Alopecia-progressive neurological defect-endocrinopathy syndrome", "alopecia-progressive neurological defect-endocrinopathy syndrome", "alopecia, progressive neurological defect, endocrinopathy syndrome", "Alopecia, progressive neurological defect, endocrinopathy syndrome", "ANE (alopecia, progressive neurological defect, endocrinopathy) syndrome", "Alopecia, progressive neurological defect, endocrinopathy syndrome (disorder)", "alopecia, progressive neurological defect, endocrinopathy syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ANE syndrome", "shortest_name_length": 4}
{"curie": "OMIM:614122", "names": ["CHITD", "CHITOTRIOSIDASE DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 5}
{"curie": "MONDO:0042600", "names": ["Sammartino-Decreccio syndrome", "Sammartino Decreccio syndrome", "superficial annular corneal dystrophy, ichthyosis nigrans, microcephaly and mild mental subnormality"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sammartino-Decreccio syndrome", "shortest_name_length": 29}
{"curie": "UMLS:C3273096", "names": ["Gallbladder MCN", "Gallbladder Mucinous Cystic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gallbladder Mucinous Cystic Neoplasm", "shortest_name_length": 15}
{"curie": "UMLS:C4324564", "names": ["Injection site indentation", "Indentation at injection site", "Indentation at injection site (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site indentation", "shortest_name_length": 26}
{"curie": "MONDO:0004716", "names": ["Stage 0 Gastric Cancer", "stage 0 stomach cancer", "Stomach cancer stage 0", "Stomach cancer in situ", "Stage 0 Stomach Cancer", "stage 0 gastric cancer", "Gastric cancer in situ", "Gastric cancer stage 0", "gastric cancer, stage 0", "stomach cancer, stage 0", "Stomach carcinoma in situ", "gastric carcinoma stage 0", "Stage 0 Gastric Carcinoma", "stage 0 gastric carcinoma", "Gastric Carcinoma Stage 0", "stage 0 stomach carcinoma", "Gastric Carcinoma in situ", "stomach in situ carcinoma", "gastric carcinoma in situ", "Stomach carcinoma stage 0", "Gastric carcinoma stage 0", "Stomach Carcinoma in situ", "stomach carcinoma in situ", "Gastric carcinoma in situ", "Stomach Carcinoma Stage 0", "Stage 0 Stomach Carcinoma", "stomach carcinoma stage 0", "gastric carcinoma, stage 0", "Gastric Carcinoma, Stage 0", "Gastric malignancy stage 0", "Gastric malignancy in situ", "Carcinoma in situ of Stomach", "Stage 0 Carcinoma of Stomach", "carcinoma of stomach stage 0", "carcinoma in situ of stomach", "Carcinoma of Stomach Stage 0", "stage 0 carcinoma of stomach", "Carcinoma in situ of stomach", "stage 0 gastric cancer aJCC v6", "Stage 0 Gastric Cancer AJCC v6", "stage 0 gastric cancer aJCC v7", "Stage 0 Gastric Cancer AJCC v7", "Carcinoma in situ of the Stomach", "Stage 0 Carcinoma of the Stomach", "stage 0 gastric (stomach) cancer", "carcinoma of the stomach stage 0", "stage 0 carcinoma of the stomach", "Carcinoma of the Stomach Stage 0", "carcinoma in situ of the stomach", "Stage 0 Gastric (Stomach) Cancer", "Carcinoma in situ of stomach, NOS", "stage 0 gastric carcinoma in situ", "stage 0 gastric cancer aJCC v6 and v7", "Stage 0 Gastric Cancer AJCC v6 and v7", "Carcinoma in situ of stomach (disorder)", "carcinoma in situ of stomach (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stomach carcinoma in situ", "shortest_name_length": 22}
{"curie": "UMLS:C4329381", "names": ["B Acute Lymphoblastic Leukemia, BCR-ABL1-Like", "B-Cell Acute Lymphoblastic Leukemia, BCR-ABL1-Like", "B-ALL with Translocations Involving Tyrosine Kinases or Cytokine Receptors", "B Acute Lymphoblastic Leukemia with Translocations Involving Tyrosine Kinases or Cytokine Receptors"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B Acute Lymphoblastic Leukemia, BCR-ABL1-Like", "shortest_name_length": 45}
{"curie": "MONDO:0013472", "names": ["myofibrillar myopathy type 7", "fatal infantile hypertonic myofibrillar myopathy", "Fatal infantile hypertonic myofibrillar myopathy", "MFM, fatal infantile hypertonic, alpha-B crystallin-related", "Fatal infantile hypertonic myofibrillar myopathy (disorder)", "MFM, FATAL INFANTILE HYPERTONIC, ALPHA-B CRYSTALLIN-RELATED", "alpha-B crystalin-related fatal infantile hypertonic myofibrillar myopathy", "MYOPATHY, MYOFIBRILLAR, FATAL INFANTILE HYPERTONIC, ALPHA-B CRYSTALLIN-RELATED", "myopathy, myofibrillar, fatal infantile hypertonic, alpha-B crystallin-related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fatal infantile hypertonic myofibrillar myopathy", "shortest_name_length": 28}
{"curie": "MONDO:0022574", "names": ["biliary atresia intrahepatic syndromic form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "biliary atresia intrahepatic syndromic form", "shortest_name_length": 43}
{"curie": "UMLS:C1707448", "names": ["Breast Columnar Cell Lesion", "Columnar Cell Lesion of Breast", "Columnar Cell Lesion of the Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Columnar Cell Lesion", "shortest_name_length": 27}
{"curie": "MONDO:0017578", "names": ["disorder of thiamine metabolism and transport"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of thiamine metabolism and transport", "shortest_name_length": 45}
{"curie": "MONDO:0030031", "names": ["LIS10", "LISSENCEPHALY 10", "lissencephaly 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lissencephaly 10", "shortest_name_length": 5}
{"curie": "UMLS:C0280192", "names": ["Recurrent Burkitt Lymphoma", "recurrent adult Burkitt lymphoma", "Recurrent Adult Burkitt Lymphoma", "Recurrent Adult Burkitt's Lymphoma", "relapsed adult small noncleaved cell lymphoma", "adult small noncleaved cell lymphoma, relapsed", "adult small noncleaved cell lymphoma, recurrent", "small noncleaved cell lymphoma, recurrent, adult", "small noncleaved cell lymphoma, adult, recurrent", "Recurrent Adult Diffuse Small Non-Cleaved Cell Lymphoma", "Relapsed Adult Small Non-Cleaved Cell/Burkitt's Lymphoma", "Recurrent Adult Small Non-Cleaved Cell/Burkitt's Lymphoma", "recurrent adult diffuse small noncleaved cell/Burkitt's lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Adult Burkitt Lymphoma", "shortest_name_length": 26}
{"curie": "UMLS:C1955864", "names": ["Cardiac Sinus Pause", "Cardiac Sinus Pauses", "Sinus Pause, Cardiac", "Cardiac Sinus Arrest", "Sinus Arrest, Cardiac", "Sinus Pauses, Cardiac", "Cardiac Sinus Arrests", "Sinus Arrests, Cardiac"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinus Arrest, Cardiac", "shortest_name_length": 19}
{"curie": "UMLS:C0855091", "names": ["Stage I B-Cell Lymphoma", "B-cell lymphoma stage I", "Stage I B-Cell Non-Hodgkin Lymphoma", "Stage I B-Cell Non-Hodgkin's Lymphoma", "Ann Arbor Stage I B-Cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-cell lymphoma stage I", "shortest_name_length": 23}
{"curie": "UMLS:C5204551", "names": ["Peritoneal Surface Disease", "Peritoneal Surface Disease Finding"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peritoneal Surface Disease Finding", "shortest_name_length": 26}
{"curie": "UMLS:C0279270", "names": ["Lip and Oral Cavity Cancer Stage 0", "stage 0 lip and oral cavity cancer", "Stage 0 Lip and Oral Cavity Cancer", "oral cavity and lip cancer, stage 0", "lip and oral cavity cancer, stage 0", "Lip and Oral Cavity Carcinoma Stage 0", "Stage 0 Lip and Oral Cavity Carcinoma", "Stage 0 Lip and Oral Cavity Cancer AJCC v7", "Stage 0 Lip and Oral Cavity Cancer AJCC v6", "stage 0 lip and oral cavity carcinoma in situ", "Stage 0 Lip and Oral Cavity Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Lip and Oral Cavity Cancer AJCC v6 and v7", "shortest_name_length": 34}
{"curie": "UMLS:C0278545", "names": ["Dukes C rectal cancer", "Rectal cancer Dukes C", "rectum cancer, Dukes C", "rectal cancer, Dukes C", "stage III rectum cancer", "stage III rectal cancer", "Stage III Rectal Cancer", "Rectal cancer stage III", "Dukes C Rectal Carcinoma", "rectum cancer, stage III", "rectal cancer, stage III", "Rectal carcinoma stage III", "Carcinoma rectum stage III", "Dukes C Carcinoma of Rectum", "Carcinoma of rectum stage III", "Rectal Cancer Stage III AJCC v6", "AJCC Stage III Rectal Cancer v6", "Stage III Rectal Cancer AJCC v6", "Dukes C Carcinoma of the Rectum", "Stage III Rectal Carcinoma AJCC v6", "Stage III Carcinoma of Rectum AJCC v6", "Stage III Carcinoma of the Rectum AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Rectal Cancer AJCC v6", "shortest_name_length": 21}
{"curie": "MONDO:0002204", "names": ["Transient arthritis", "transient arthritis", "arthritis; transient", "transient; arthritis", "transient arthropathy", "Transient arthropathy", "Transient Arthropathy", "transient; arthropathy", "arthropathy; transient", "Transient arthritis (disorder)", "Transient arthropathy (disorder)", "transient arthropathy (diagnosis)", "Transient arthropathy, site unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transient arthritis", "shortest_name_length": 19}
{"curie": "UMLS:C0036679", "names": ["Diastasis", "diastasis", "Separation", "separation", "Separation, NOS", "Physical detachment", "Separation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diastasis", "shortest_name_length": 9}
{"curie": "MONDO:0054776", "names": ["FFEVF4", "EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 4", "epilepsy, familial focal, with variable foci 4", "epilepsy, FAMILIAL focal, with variable foci 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, familial focal, with variable foci 4", "shortest_name_length": 6}
{"curie": "MONDO:0017328", "names": ["non-CNS-localized embryonal carcinoma", "non-central nervous system-localized embryonal carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-central nervous system-localized embryonal carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0001708", "names": ["lung sarcoid", "Lung sarcoid", "lung sarcoidosis", "Lung Sarcoidosis", "sarcoidosis lung", "lung Sarcoidosis", "sarcoidosis; lung", "lung; sarcoidosis", "lungs sarcoidosis", "Sarcoidosis of lung", "sarcoidosis of lung", "sarcoidosis pulmonary", "Pulmonary Sarcoidoses", "SARCOIDOSIS PULMONARY", "Pulmonary sarcoidosis", "pulmonary sarcoidosis", "Pulmonary Sarcoidosis", "Sarcoidosis, Pulmonary", "Sarcoidosis, pulmonary", "Sarcoidoses, Pulmonary", "lung; disease, in sarcoidosis", "Pulmonary sarcoidosis (disorder)", "sarcoidosis with lung involvement", "disease (or disorder); lung, in sarcoidosis", "sarcoidosis with lung involvement (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary sarcoidosis", "shortest_name_length": 12}
{"curie": "MONDO:0012307", "names": ["familial scaphocephaly syndrome, McGillivray type", "scaphocephaly, maxillary retrusion, and mental retardation", "Scaphocephaly, Maxillary Retrusion, And Mental Retardation", "SCAPHOCEPHALY, MAXILLARY RETRUSION, AND MENTAL RETARDATION", "scaphocephaly, maxillary retrusion, and intellectual disability", "SCAPHOCEPHALY, MAXILLARY RETRUSION, AND IMPAIRED INTELLECTUAL DEVELOPMENT", "SCAPHOCEPHALY, MAXILLARY RETRUSION, AND INTELLECTUAL DEVELOPMENTAL DISORDER", "scaphocephaly-macrocephaly-maxillary retrusion-intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial scaphocephaly syndrome, McGillivray type", "shortest_name_length": 49}
{"curie": "UMLS:C0334447", "names": ["MBN", "Malignant Blue Nevus", "Malignant blue nevus", "Blue nevus, malignant", "Malignant blue naevus", "Blue naevus, malignant", "Blue nevus-like melanoma", "[M]Blue nevus, malignant", "Blue Nevus-Like Melanoma", "[M]Blue naevus, malignant", "Malignant Skin Blue Nevus", "Blue naevus-like melanoma", "Malignant Blue Nevus of Skin", "Malignant blue nevus of skin", "malignant blue nevus of skin", "Malignant blue naevus of skin", "Malignant Cutaneous Blue Nevus", "Malignant melanoma in blue nevus", "Melanoma Arising from Blue Nevus", "Melanoma arising from blue nevus", "Malignant Blue Nevus of the Skin", "Malignant melanoma in blue naevus", "Malignant blue nevus of skin (disorder)", "malignant blue nevus of skin (diagnosis)", "Blue nevus, malignant (morphologic abnormality)", "Cutaneous (Skin) Melanoma Arising from Blue Nevus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant blue nevus of skin", "shortest_name_length": 3}
{"curie": "MONDO:0003493", "names": ["Epidermoid Thymic carcinoma", "Epidermoid Thymic Carcinoma", "epidermoid thymic carcinoma", "thymic squamous cell carcinoma", "Thymus Squamous Cell Carcinoma", "Thymus squamous cell carcinoma", "Thymic Squamous Cell Carcinoma", "thymus squamous cell carcinoma", "Squamous Cell Carcinoma of Thymus", "squamous cell carcinoma of Thymus", "squamous cell carcinoma of thymus", "squamous cell carcinoma of the Thymus", "Squamous Cell Carcinoma of the Thymus", "squamous cell carcinoma of thymus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thymus squamous cell carcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0016534", "names": ["infundibulo-neurohypophysitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infundibulo-neurohypophysitis", "shortest_name_length": 29}
{"curie": "UMLS:C0012359", "names": ["Ectasia", "ectasia", "ectasias", "Dilation", "dilation", "Distention", "Distension", "DILATATION", "Dilatation", "Dilatations", "Distension, NOS", "Distention, NOS", "Dilatation, NOS", "abnormal dilation", "pathologic dilatation", "Pathologic Dilatation", "Pathologic Dilatations", "Dilatation, Pathologic", "Pathological Dilatation", "Dilatations, Pathologic", "Dilatation, Pathological", "Pathological Dilatations", "Dilatations, Pathological", "Dilatation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathological Dilatation", "shortest_name_length": 7}
{"curie": "MONDO:0001367", "names": ["chronic congestive splenomegaly", "Chronic congestive splenomegaly", "congestive splenomegaly, chronic", "SPLENOMEGALY, CONGESTIVE CHRONIC", "chronic; congestive, splenomegaly", "splenomegaly; congestive, chronic", "Chronic congestive splenomegaly (disorder)", "chronic congestive splenomegaly (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic congestive splenomegaly", "shortest_name_length": 31}
{"curie": "MONDO:0001037", "names": ["ring corneal ulcer", "Ring corneal ulcer", "Ring corneal ulcer (disorder)", "ring corneal ulcer (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ring corneal ulcer", "shortest_name_length": 18}
{"curie": "UMLS:C5204272", "names": ["Kidney Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kidney Neuroendocrine Carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0020451", "names": ["Congenital stenosis of the IVC", "congenital stenosis of the IVC", "Congenital inferior vena cava stenosis", "Congenital narrowed posterior vena cava", "Congenital stenosis of inferior vena cava", "Congenital stenosis of the inferior vena cava", "congenital stenosis of the inferior vena cava", "congenital stenosis of the inferior caval vein", "Congenital stenosis of the inferior caval vein", "Congenital stenosis of inferior vena cava (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital stenosis of the inferior vena cava", "shortest_name_length": 30}
{"curie": "MONDO:0001169", "names": ["spastic monoplegia", "Congenital monoplegia", "spastic monoplegic cerebral palsy", "infantile monoplegic cerebral palsy", "monoplegic infantile cerebral palsy", "Monoplegic infantile cerebral palsy", "Monoplegic Infantile Cerebral Palsy", "Infantile cerebral palsy, monoplegic", "Infantile Cerebral Palsy, Monoplegic", "Cerebral Palsy, Monoplegic, Infantile"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic monoplegia", "shortest_name_length": 18}
{"curie": "UMLS:C0393698", "names": ["Cryptogenic West Syndrome", "Cryptogenic West syndrome", "West Syndrome, Cryptogenic", "Syndrome, Cryptogenic West", "Cryptogenic Infantile Spasm", "Infantile Spasm, Cryptogenic", "Spasm, Cryptogenic Infantile", "Cryptogenic Infantile Spasms", "Infantile Spasms, Cryptogenic", "Spasms, Cryptogenic Infantile", "Cryptogenic West syndrome (disorder)", "Cryptogenic West syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cryptogenic Infantile Spasms", "shortest_name_length": 25}
{"curie": "UMLS:C4526902", "names": ["Stage IB Soft Tissue Sarcoma of the Trunk and Extremities", "Stage IB Soft Tissue Sarcoma of the Trunk and Extremities AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Soft Tissue Sarcoma of the Trunk and Extremities AJCC v8", "shortest_name_length": 57}
{"curie": "MONDO:0019496", "names": ["NEN", "APUDoma", "Neuroendocrine Tumor", "neuroendocrine tumor", "Neuroendocrine tumor", "Tumor, Neuroendocrine", "neuroendocrine tumour", "NEUROENDOCRINE TUMORS", "Neuroendocrine tumour", "Neuroendocrine tumors", "Neuroendocrine Tumors", "neuroendocrine tumors", "neuroendocrine tumours", "Tumors, Neuroendocrine", "Neuroendocrine Neoplasm", "neuroendocrine neoplasm", "Neuroendocrine neoplasm", "Neuroendocrine neoplasia", "Neuroendocrine tumor NOS", "neoplasms neuroendocrine", "Neuroendocrine tumor (disorder)", "neuroendocrine tumor (diagnosis)", "Neuroendocrine tumor (morphologic abnormality)", "Neuroendocrine neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuroendocrine neoplasm", "shortest_name_length": 3}
{"curie": "MONDO:0012462", "names": ["Frontotemporal pachygyria", "Pachygyria, frontotemporal", "PACHYGYRIA, FRONTOTEMPORAL", "pachygyria, frontotemporal", "autosomal recessive frontotemporal pachygyria", "Autosomal recessive frontotemporal pachygyria", "Autosomal recessive frontotemporal pachygyria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive frontotemporal pachygyria", "shortest_name_length": 25}
{"curie": "MONDO:0004122", "names": ["thymic small cell carcinoma", "Thymus small cell carcinoma", "thymus small cell carcinoma", "Thymus Small Cell Carcinoma", "Thymic Small Cell Carcinoma", "small cell carcinoma of thymus", "small cell carcinoma of Thymus", "Small Cell Carcinoma of Thymus", "small cell carcinoma of the Thymus", "Small Cell Carcinoma of the Thymus", "Thymic Small Cell Neuroendocrine Carcinoma", "thymic small cell carcinoma neuroendocrine type", "Thymic Small Cell Carcinoma Neuroendocrine Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thymus small cell carcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0005624", "names": ["Gull", "Gull disease", "gull disease", "GULL DISEASE", "Atrophic thyroiditis", "atrophic thyroiditis", "Idiopathic atrophic myxedema", "Idiopathic atrophic myxoedema", "Idiopathic atrophic hypothyroidism", "Idiopathic atrophic hypothyroidism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrophic thyroiditis", "shortest_name_length": 4}
{"curie": "UMLS:C2931254", "names": ["Alport syndrome, recessive type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alport syndrome, recessive type", "shortest_name_length": 31}
{"curie": "MONDO:0018339", "names": ["PrP systemic amyloidosis", "chronic diarrhea with HSAN", "Chronic diarrhea with HSAN", "Prion protein systemic amyloidosis", "prion protein systemic amyloidosis", "PrP (prion protein) systemic amyloidosis", "Prion protein systemic amyloidosis (disorder)", "Chronic diarrhea with hereditary sensory and autonomic neuropathy", "chronic diarrhea with hereditary sensory and autonomic neuropathy", "Chronic diarrhoea with hereditary sensory and autonomic neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PrP systemic amyloidosis", "shortest_name_length": 24}
{"curie": "UMLS:C5670584", "names": ["Childhood Spinal Ependymoma", "Childhood Spinal Cord Ependymoma", "Pediatric Spinal Cord Ependymoma", "Childhood Spinal Cord Ependymoma without MYCN Amplification"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Spinal Cord Ependymoma", "shortest_name_length": 27}
{"curie": "MONDO:0021921", "names": ["Arnold Stickler Bourne syndrome", "Arnold stickler bourne syndrome", "corneal crystals myopathy and neuropathy", "Corneal crystals myopathy and nephropathy", "corneal crystals myopathy and nephropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arnold stickler bourne syndrome", "shortest_name_length": 31}
{"curie": "UMLS:C0269815", "names": ["parturition complication", "labor delivery complications", "complications of labor delivery", "Labor and Delivery Complication", "complications of labor and delivery", "Complications of labor and delivery", "Complications of labour and delivery", "parturition complication (diagnosis)", "Complication of labor and delivery, NOS", "Complication of labour and delivery, NOS", "Complications of labor and delivery (O60-O77)", "Unspecified complication of labor and delivery", "Complication of labor and delivery, unspecified", "Complication of labour and delivery, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Complication of labor and delivery, unspecified", "shortest_name_length": 24}
{"curie": "UMLS:C2748388", "names": ["Complication associated with device", "Complications associated with device", "Complication associated with device (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Complication associated with device", "shortest_name_length": 35}
{"curie": "MONDO:0018242", "names": ["Autoimmune hypoparathyroidism", "autoimmune hypoparathyroidism", "Hypoparathyroidism, autoimmune", "autoimmune hypoparathyroidism (disease)", "Autoimmune hypoparathyroidism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune hypoparathyroidism", "shortest_name_length": 29}
{"curie": "UMLS:C0274724", "names": ["quinidine toxicity", "Quinidine poisoning", "Poisoning by quinidine", "Poisoning caused by quinidine", "quinidine toxicity (diagnosis)", "Poisoning caused by quinidine (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Poisoning by quinidine", "shortest_name_length": 18}
{"curie": "MONDO:0004564", "names": ["thyroid malformation", "Thyroid malformation", "Thyroid Malformation", "Thyroid malformation NOS", "Thyroid Gland Malformation", "thyroid gland malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid malformation", "shortest_name_length": 20}
{"curie": "MONDO:0013515", "names": ["OI6", "OI type 6", "OI type VI", "OI, Type VI", "osteogenesis imperfecta type", "OI6 Osteogenesis imperfecta 6", "osteogenesis imperfecta type 6", "Osteogenesis imperfecta, type 6", "osteogenesis imperfecta type VI", "osteogenesis imperfecta, type 6", "SERPINF1 osteogenesis imperfecta", "osteogenesis imperfecta, type VI", "OSTEOGENESIS IMPERFECTA, TYPE VI", "Osteogenesis Imperfecta, Type VI", "SERPINFI- related osteogenesis imperfecta", "OI, type 6 Osteogenesis imperfecta, type 6", "OI, type VI Osteogenesis imperfecta, type VI", "osteogenesis imperfecta caused by mutation in SERPINF1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteogenesis imperfecta type 6", "shortest_name_length": 3}
{"curie": "UMLS:C4763396", "names": ["Refractory Primary Diffuse Large B-Cell Lymphoma of the Central Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Primary Diffuse Large B-Cell Lymphoma of the Central Nervous System", "shortest_name_length": 78}
{"curie": "UMLS:C5555177", "names": ["Refractory Fallopian Tube Undifferentiated Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Fallopian Tube Undifferentiated Carcinoma", "shortest_name_length": 52}
{"curie": "MONDO:0030362", "names": ["AGS9", "AICARDI-GOUTIERES SYNDROME 9", "Aicardi-Goutieres syndrome 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aicardi-Goutieres syndrome 9", "shortest_name_length": 4}
{"curie": "MONDO:0012200", "names": ["Ppcd3", "PPCD3", "posterior polymorphous corneal dystrophy 3", "Corneal Dystrophy, Posterior Polymorphous, 3", "CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 3", "corneal dystrophy, POSTERIOR polymorphous, 3", "ZEB1 posterior polymorphous corneal dystrophy", "posterior polymorphous corneal dystrophy type 3", "corneal dystrophy, posterior polymorphous, type 3", "CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 3 (disorder)", "posterior polymorphous corneal dystrophy caused by mutation in ZEB1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "posterior polymorphous corneal dystrophy 3", "shortest_name_length": 5}
{"curie": "UMLS:C0877092", "names": ["Venipuncture site bruise"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Venipuncture site bruise", "shortest_name_length": 24}
{"curie": "MONDO:0044627", "names": ["AMNR", "acute macular neuroretinopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute macular neuroretinopathy", "shortest_name_length": 4}
{"curie": "MONDO:0004828", "names": ["Lower urinary tract calculus", "lower urinary tract calculus", "calculus; urinary tract, lower", "Calculus of lower urinary tract", "lower urinary tract urolithiasis", "urolithiasis; lower urinary tract", "urolithiasis of lower urinary tract", "Calculus of lower urinary tract, NOS", "lower urinary tract calculus (diagnosis)", "Calculus of lower urinary tract (disorder)", "Calculus of lower urinary tract, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lower urinary tract calculus", "shortest_name_length": 28}
{"curie": "UMLS:C4505163", "names": ["Food Addiction", "Food Addictions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Food Addiction", "shortest_name_length": 14}
{"curie": "MONDO:0013435", "names": ["CILD15", "Primary Ciliary Dyskinesia 15", "primary ciliary dyskinesia 15", "ciliary dyskinesia, primary, 15", "CILIARY DYSKINESIA, PRIMARY, 15", "CCDC40 primary ciliary dyskinesia", "primary ciliary dyskinesia type 15", "ciliary dyskinesia, primary, type 15", "primary ciliary dyskinesia caused by mutation in CCDC40", "primary ciliary dyskinesia 15 with or without situs inversus", "ciliary dyskinesia, primary, 15, with or without situs inversus", "CILIARY DYSKINESIA, PRIMARY, 15, WITH OR WITHOUT SITUS INVERSUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia 15", "shortest_name_length": 6}
{"curie": "MONDO:0010995", "names": ["CMT1C", "CMT 1C", "HMSNIC", "HMSN1C", "HMSN IC", "HMSN 1C", "CMT slow nerve conduction type C", "CMT, slow nerve conduction type C", "CMT, Slow Nerve Conduction Type C", "CMT, SLOW NERVE CONDUCTION TYPE C", "Charcot-Marie-Tooth disease type 1C", "Charcot Marie Tooth disease type 1C", "Charcot-Marie-Tooth disease, Type 1C", "Charcot-Marie-Tooth disease, type IC", "CHARCOT-MARIE-TOOTH DISEASE, TYPE 1C", "Charcot-Marie-Tooth disease, type 1C", "Charcot-Marie-Tooth neuropathy type 1C", "Charcot-Marie-Tooth neuropathy, type 1C", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 1C", "LITAF Charcot-Marie-Tooth disease type 1", "Charcot-Marie-Tooth disease, type IC (disorder)", "Charcot-Marie-Tooth disease type 1C (diagnosis)", "neuropathy hereditary motor and sensory type 1C", "NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE IC", "neuropathy, hereditary motor and sensory, type 1C", "Charcot-Marie-Tooth disease, demyelinating, Type 1C", "CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1C", "Charcot-Marie-Tooth disease, demyelinating, type 1C", "Charcot-Marie-Tooth disease type 1 caused by mutation in LITAF", "Charcot-Marie-Tooth Neuropathy, Type 1C Neuropathy, Hereditary Motor And Sensory, Type IC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 1C", "shortest_name_length": 5}
{"curie": "UMLS:C1332041", "names": ["AIDS-Related Cryptococcosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Cryptococcosis", "shortest_name_length": 27}
{"curie": "EFO:0008536", "names": ["anti-centromere-antibody-positive systemic scleroderma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anti-centromere-antibody-positive systemic scleroderma", "shortest_name_length": 54}
{"curie": "UMLS:C4683240", "names": ["Pathologic Stage IV Retinoblastoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IV Retinoblastoma AJCC v8", "shortest_name_length": 42}
{"curie": "UMLS:C4684823", "names": ["Lung Malignant PEComa", "Malignant Lung PEComa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Malignant PEComa", "shortest_name_length": 21}
{"curie": "UMLS:C1333274", "names": ["Dental and Periodontal Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dental and Periodontal Infection", "shortest_name_length": 32}
{"curie": "UMLS:C1334676", "names": ["Mediastinal Rhabdomyoma", "Rhabdomyoma of Mediastinum", "Rhabdomyoma of the Mediastinum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mediastinal Rhabdomyoma", "shortest_name_length": 23}
{"curie": "MONDO:0018150", "names": ["gaucher disease", "disease gaucher", "Gaucher disease", "Gaucher Disease", "GAUCHER DISEASE", "gaucher syndrome", "gauchers disease", "Gaucher syndrome", "Disease, Gaucher", "Gaucher Syndrome", "disease gauchers", "Gauchers Disease", "Gaucher's Disease", "gaucher's disease", "Gaucher's disease", "Disease, Gauchers", "Gauchers Diseases", "disease gaucher's", "Syndrome, Gaucher", "Kerasin lipoidosis", "Kerasin Lipoidosis", "sphingolipidosis 1", "Diseases, Gauchers", "Disease, Gaucher's", "kerasin lipoidosis", "Kerasin Lipoidoses", "Lipoidosis, Kerasin", "Glucocerebrosidoses", "Lipoidoses, Kerasin", "Glucocerebrosidosis", "glucocerebrosidosis", "Gaucher Splenomegaly", "Gaucher splenomegaly", "Kerasin histiocytosis", "Adult Gaucher disease", "Kerasin Histiocytosis", "cerebroside lipidosis", "kerasin histiocytosis", "Splenomegaly, Gaucher", "Kerasin Histiocytoses", "Histiocytosis, Kerasin", "Kerasin thesaurismosis", "kerasin thesaurismosis", "lipidosis; cerebroside", "Histiocytoses, Kerasin", "Kerasin thesaurismoses", "Gaucher disease type I", "Gaucher's disease, NOS", "LIPIDOSIS, CEREBROSIDE", "cerebroside; lipidosis", "thesaurismoses, Kerasin", "familial splenic anemia", "thesaurismosis, Kerasin", "splenomegaly; gaucher's", "Gaucher's disease, type I", "ANEMIA, SPLENIC, FAMILIAL", "Glucosylceramide Lipidoses", "glucosylceramide lipidosis", "Glucosylceramide Lipidosis", "Lipidosis, Glucosylceramide", "Lipidoses, Glucosylceramide", "Gaucher disease (diagnosis)", "glucosylceramidase deficiency", "Glucocerebrosidase Deficiency", "Glucocerebrosidase deficiency", "Glucosylceramidase Deficiency", "glocucerebrosidase deficiency", "Glucosylceramidase deficiency", "glucocerebrosidase deficiency", "Cerebroside lipidosis syndrome", "Glucosyl Cerebroside Lipidoses", "glucosyl cerebroside lipidosis", "acute cerebral Gaucher disease", "Glucosyl Cerebroside Lipidosis", "Glucosyl cerebroside lipidosis", "GLUCOSYL CEREBROSIDE LIPIDOSIS", "Cerebroside Lipidosis Syndrome", "cerebroside lipidosis syndrome", "Deficiency, Glucocerebrosidase", "Glucocerebrosidase Deficiencies", "Lipidosis Syndrome, Cerebroside", "Lipidosis, Glucosyl Cerebroside", "Cerebroside Lipidosis, Glucosyl", "Cerebroside Lipidosis Syndromes", "Chronic adult Gaucher's disease", "Cerebroside Lipidoses, Glucosyl", "Lipidoses, Glucosyl Cerebroside", "Syndrome, Cerebroside Lipidosis", "Lipidosis Syndromes, Cerebroside", "Deficiencies, Glucocerebrosidase", "Acid beta-glucosidase deficiency", "Acid beta-Glucosidase Deficiency", "Syndromes, Cerebroside Lipidosis", "acid beta-glucosidase deficiency", "Kerasin thesaurismosis (disorder)", "Gaucher disease type I (diagnosis)", "HISTIOCYTOSIS, LIPID, KERASIN TYPE", "lipoid histiocytosis (kerasin type)", "Lipoid Histiocytoses (Kerasin Type)", "Lipoid Histiocytosis (Kerasin Type)", "Histiocytosis, Lipoid (Kerasin Type)", "Glucocerebrosidase deficiency type I", "Histiocytoses, Lipoid (Kerasin Type)", "Glucocerebrosidase Deficiency Disease", "Deficiency Disease, Glucocerebrosidase", "Glucocerebrosidase Deficiency Diseases", "Disease, Glucocerebrosidase Deficiency", "Diseases, Glucocerebrosidase Deficiency", "Deficiency Diseases, Glucocerebrosidase", "Chronic non-neuropathic Gaucher disease", "Acid beta-Glucosidase Deficiency Disease", "Chronic non-neuropathic Gaucher's disease", "CEREBROSIDE LIPOIDOSIS GAUCHERS ADULT FORM", "Glucosylceramidase deficiency, chronic type", "CEREBROSIDE LIPOIDOSIS <GAUCHERS ADULT FORM>", "Glucosylceramide Beta-Glucosidase Deficiency", "Glucosylceramide beta-glucosidase deficiency", "glucosylceramide beta-glucosidase deficiency", "Glucosylceramide Beta-Glucosidase Deficiency Disease", "Chronic non-neuropathic Gaucher's disease (disorder)", "Glucosylceramide beta-glucosidase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gaucher disease", "shortest_name_length": 15}
{"curie": "UMLS:C4683608", "names": ["Lugano Classification Stage IE Adult Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage IE Adult Hodgkin Lymphoma AJCC v8", "shortest_name_length": 61}
{"curie": "MONDO:0004188", "names": ["Iris Spindle Cell Melanoma", "iris spindle cell melanoma", "Spindle Cell Melanoma of Iris", "spindle cell melanoma of iris", "spindle cell melanoma of the iris", "Spindle Cell Melanoma of the Iris"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "iris spindle cell melanoma", "shortest_name_length": 26}
{"curie": "MONDO:0019330", "names": ["Pili gemini", "pili gemini", "Compound hairs", "Pili multigemini", "pili multigemini", "Pili multigemini (disorder)", "Multiple hairs per follicle"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pili gemini", "shortest_name_length": 11}
{"curie": "UMLS:C5446447", "names": ["Lacrimal Drainage System Carcinoma", "Carcinoma of the Lacrimal Drainage System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lacrimal Drainage System Carcinoma", "shortest_name_length": 34}
{"curie": "UMLS:C1096036", "names": ["Infusion site warmth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infusion site warmth", "shortest_name_length": 20}
{"curie": "MONDO:0005565", "names": ["Embryoma", "blastoma", "Blastoma", "embryoma", "Blastoma, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blastoma", "shortest_name_length": 8}
{"curie": "UMLS:C0521465", "names": ["TOXICODERMA", "toxicoderma", "Toxicoderma", "toxicodermia", "Toxicodermia", "Toxicodermatosis", "Toxicoderma, NOS", "toxicodermatosis", "toxic skin eruption", "Toxic skin eruption", "eruption; skin, toxic", "Toxicodermatosis, NOS", "skin; eruption, toxic", "Toxicoderma (disorder)", "Dermatosis due to poison"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Toxicoderma", "shortest_name_length": 11}
{"curie": "MONDO:0001285", "names": ["endometriosis of pelvic peritoneum", "Endometriosis of pelvic peritoneum", "Endometriosis of pelvic peritoneum (disorder)", "endometriosis of pelvic peritoneum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometriosis of pelvic peritoneum", "shortest_name_length": 34}
{"curie": "MONDO:0003875", "names": ["pediatric central nervous system mature teratoma", "Childhood Central Nervous System Mature Teratoma", "childhood central nervous system mature teratoma", "central nervous system mature teratoma of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood central nervous system mature teratoma", "shortest_name_length": 48}
{"curie": "MONDO:0001562", "names": ["HIATAL HERNIA CONGENITAL", "Hiatus hernia congenital", "congenital hiatus hernia", "Congenital hiatal hernia", "congenital hiatal hernia", "Congenital hiatus hernia", "congenital hernia hiatal", "hernia; hiatal, congenital", "hiatal; hernia, congenital", "Congenital hiatus hernia (disorder)", "congenital hiatus hernia (diagnosis)", "displacement; cardia through esophageal hiatus", "cardia through esophageal hiatus; displacement", "Displacement of cardia through esophageal hiatus", "displacement of cardia through esophageal hiatus", "Congenital displacement of cardia through esophageal hiatus", "Congenital displacement of cardia through oesophageal hiatus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "displacement of cardia through esophageal hiatus", "shortest_name_length": 24}
{"curie": "MONDO:0000290", "names": ["Naegleria fowleri infection", "Naegleria fowleri Infection", "Infection, Naegleria fowleri", "Naegleria fowleri Infections", "infections, Naegleria fowleri", "Primary amebic meningoencephalitis", "infection due to Naegleria fowleri", "primary amebic meningoencephalitis", "Primary Amebic Meningoencephalitis", "Primary amoebic meningoencephalitis", "Amebic Meningoencephalitis, Primary", "Meningoencephalitis, Primary Amebic", "MENINGOENCEPHALITIS, PRIMARY AMEBIC", "Primary Amebic Meningoencephalitides", "Amebic Meningoencephalitides, Primary", "Naegleria fowleri Meningoencephalitis", "Infection caused by Naegleria fowleri", "Meningoencephalitides, Primary Amebic", "Meningoencephalitis, Naegleria fowleri", "Naegleria fowleri Meningoencephalitides", "Meningoencephalitides, Naegleria fowleri", "[OBSOLETE] Primary amebic meningoencephalitis", "infection due to Naegleria fowleri (diagnosis)", "Infection caused by Naegleria fowleri (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary amebic meningoencephalitis", "shortest_name_length": 27}
{"curie": "MONDO:0011730", "names": ["FMRD", "Fumaricaciduria", "fumaric aciduria", "FUMARIC ACIDURIA", "Fumaric aciduria", "Fumarase deficiency", "FUMARASE DEFICIENCY", "fumarase deficiency", "Deficiency of fumarase", "fumarate hydratase deficiency", "Fumarate Hydratase Deficiency", "Fumarase deficiency (disorder)", "Deficiency of fumarate hydratase", "Deficiency of fumarate hydratase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fumaric aciduria", "shortest_name_length": 4}
{"curie": "MONDO:0013708", "names": ["MRT25", "mental retardation, autosomal recessive 25", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 25", "intellectual disability, autosomal recessive 25", "autosomal recessive intellectual developmental disorder 25", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 25"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 25", "shortest_name_length": 5}
{"curie": "UMLS:C0018805", "names": ["Heart Injury", "Heart injury", "injury heart", "heart injury", "Injury, Heart", "heart; injury", "injury; heart", "heart injuries", "Heart Injuries", "Injuries, Heart", "Injury of heart", "Heart injury NOS", "Injury of heart, NOS", "heart injury (diagnosis)", "Injury of heart (disorder)", "Injury of heart, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Heart Injuries", "shortest_name_length": 12}
{"curie": "UMLS:C5418774", "names": ["Recurrent Fallopian Tube Transitional Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Fallopian Tube Transitional Cell Carcinoma", "shortest_name_length": 52}
{"curie": "MONDO:0022458", "names": ["annular constricting bands"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "annular constricting bands", "shortest_name_length": 26}
{"curie": "MONDO:0022815", "names": ["congenital absence of the sternocleidomastoid muscle", "Congenital absence of the sternocleidomastoid muscle"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital absence of the sternocleidomastoid muscle", "shortest_name_length": 52}
{"curie": "MONDO:0014930", "names": ["MRT56", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 56", "mental retardation, autosomal recessive 56", "intellectual disability, autosomal recessive 56", "mental retardation, autosomal recessive type 56", "intellectual disability, autosomal recessive type 56", "autosomal recessive intellectual developmental disorder 56", "intellectual developmental disorder, autosomal recessive 56", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 56", "ZC3H14 autosomal recessive non-syndromic intellectual disability", "autosomal recessive non-syndromic intellectual disability caused by mutation in ZC3H14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 56", "shortest_name_length": 5}
{"curie": "MONDO:0005691", "names": ["Cardiovirus Infection", "Cardiovirus infection", "Cardiovirus Infections", "Infection, Cardiovirus", "infection, Cardiovirus", "Infections, Cardiovirus", "infections, Cardiovirus", "Cardiovirus infectious disease", "cardiovirus infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiovirus infectious disease", "shortest_name_length": 21}
{"curie": "MONDO:0016012", "names": ["syndrome de", "de syndrome", "syndrome des", "DES syndrome", "des syndrome", "DES embryofetopathy", "Distilbene embryofetopathy", "diethylstilbestrol syndrome", "Diethylstilbestrol Syndrome", "Diethylstilbestrol syndrome", "Diethylstilboestrol syndrome", "DES (diethylstilbestrol) syndrome", "Fetal Diethylstilbestrol Syndrome", "Fetal diethylstilbestrol syndrome", "fetal diethylstilbestrol syndrome", "Foetal diethylstilbestrol syndrome", "Diethylstilbestrol embryofetopathy", "diethylstilbestrol embryofetopathy", "antenatal diethylstilbestrol exposure", "Fetal diethylstilbestrol syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diethylstilbestrol syndrome", "shortest_name_length": 11}
{"curie": "UMLS:C1333518", "names": ["Extraskeletal Osteoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extraskeletal Osteoma", "shortest_name_length": 21}
{"curie": "MONDO:0001878", "names": ["acquired gastric outlet stenosis", "Acquired gastric outlet stenosis", "Adult hypertrophic pyloric stenosis", "ADULT HYPERTROPHIC PYLORIC STENOSIS", "adult hypertrophic pyloric stenosis", "Acquired hypertrophic pyloric stenosis", "acquired hypertrophic pyloric stenosis", "Adult hypertrophic pyloric stenosis (disorder)", "adult hypertrophic pyloric stenosis (diagnosis)", "Acquired hypertrophic pyloric stenosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired hypertrophic pyloric stenosis", "shortest_name_length": 32}
{"curie": "MONDO:0022975", "names": ["diaphragmatic agenesis radial aplasia omphalocele"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diaphragmatic agenesis radial aplasia omphalocele", "shortest_name_length": 49}
{"curie": "UMLS:C1335161", "names": ["Ovarian Fibrosarcoma", "Fibrosarcoma of Ovary", "fibrosarcoma of ovary", "Fibrosarcoma of the Ovary", "fibrosarcoma of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibrosarcoma of ovary", "shortest_name_length": 20}
{"curie": "MONDO:0010683", "names": ["MTM", "MTM1", "MTMX", "CNMX", "XLCNM", "XLMTM", "myotubular myopathy 1", "MYOTUBULAR MYOPATHY 1", "Myotubular Myopathy 1", "myopathy myotubular x link", "X Linked Myotubular Myopathy", "x-linked myotubular myopathy", "X-Linked Myotubular Myopathy", "X-linked myotubular myopathy", "Myotubular Myopathy, X Linked", "MYOTUBULAR MYOPATHY, X-LINKED", "Myopathy, X-Linked Myotubular", "Myotubular Myopathy, X-Linked", "myotubular myopathy, X-linked", "X-Linked Myotubular Myopathies", "Myopathies, X-Linked Myotubular", "X Linked Centronuclear Myopathy", "Myotubular Myopathies, X-Linked", "X-linked centronuclear myopathy", "centronuclear myopathy X-linked", "X-Linked Centronuclear Myopathy", "Myopathy, X-Linked Centronuclear", "centronuclear myopathy, X-linked", "Centronuclear Myopathy, X-Linked", "MYOPATHY, CENTRONUCLEAR, X-LINKED", "myopathy, centronuclear, X-linked", "X-Linked Centronuclear Myopathies", "Centronuclear Myopathies, X-Linked", "Myopathies, X-Linked Centronuclear", "Severe x-linked myotubular myopathy", "Severe X-linked myotubular myopathy", "X-linked recessive myotubular myopathy", "X-linked recessive centronuclear myopathy", "X-linked myotubular myopathy (XLMTM, MTMX)", "Severe X-linked myotubular myopathy (disorder)", "myotubular myopathy, X-linked, X-linked recessive", "X-linked congenital recessive muscle hypotrophy with central nuclei"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked centronuclear myopathy", "shortest_name_length": 3}
{"curie": "UMLS:C2347923", "names": ["Refractory Brain Tumor", "Refractory Brain Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Brain Neoplasm", "shortest_name_length": 22}
{"curie": "UMLS:C3805232", "names": ["Post-PV MF", "Polycythemia Vera, \"Spent\" Phase", "Post-polycythemia vera myelofibrosis", "Post polycythemia vera myelofibrosis", "Post-polycythemia Vera Myelofibrosis", "Post polycythaemia vera myelofibrosis", "Post-polycythaemia vera myelofibrosis", "Spent Phase and Post-Polycythemic Myelofibrosis", "Myelofibrosis due to and following polycythemia vera", "Myelofibrosis due to and following polycythaemia vera", "Polycythemia Vera, Post-Polycythemic Myelofibrosis Phase", "Myelofibrosis due to and following polycythemia vera (disorder)", "Polycythemia Vera, Post-Polycythemic Myelofibrosis and Myeloid Metaplasia Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post-polycythemia vera myelofibrosis", "shortest_name_length": 10}
{"curie": "UMLS:C0854975", "names": ["Stage IV Adenosquamous Lung Cancer", "Stage IV Adenosquamous Lung Carcinoma", "Adenosquamous cell lung cancer stage IV", "Stage IV Adenosquamous Cell Lung Carcinoma", "Stage IV Adenosquamous Cell Carcinoma of Lung", "Stage IV Lung Adenosquamous Carcinoma AJCC v7", "Stage IV Adenosquamous Cell Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenosquamous cell lung cancer stage IV", "shortest_name_length": 34}
{"curie": "MONDO:0012317", "names": ["VSCN3", "ENTERIC NEUROPATHY, FAMILIAL", "Enteric Neuropathy, Familial", "enteric neuropathy, familial", "PSEUDOOBSTRUCTION, IDIOPATHIC INTESTINAL", "Pseudoobstruction, Idiopathic Intestinal", "pseudoobstruction, idiopathic intestinal", "autosomal dominant familial visceral neuropathy", "Visceral Neuropathy, Familial, Autosomal Dominant", "visceral neuropathy, familial, autosomal dominant", "Pseudoobstruction, Chronic Intestinal, Neuropathic", "PSEUDOOBSTRUCTION, CHRONIC INTESTINAL, NEUROPATHIC", "pseudoobstruction, chronic intestinal, neuropathic", "visceral neuropathy, familial, 3, autosomal dominant", "VISCERAL NEUROPATHY, FAMILIAL, 3, AUTOSOMAL DOMINANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "visceral neuropathy, familial, 3, autosomal dominant", "shortest_name_length": 5}
{"curie": "UMLS:C5555512", "names": ["Locally Recurrent Uterine Corpus Leiomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Recurrent Uterine Corpus Leiomyosarcoma", "shortest_name_length": 47}
{"curie": "UMLS:C0269155", "names": ["Germinal inclusion cyst", "germinal inclusion cyst", "Cyst, germinal inclusion", "cysts germinal inclusion", "Ovarian Germinal Inclusion Cyst", "Germinal Inclusion Cyst of Ovary", "Germinal inclusion cyst of ovary", "Germinal epithelial inclusion cyst", "Germinal Inclusion Cyst of the Ovary", "benign germinal inclusion cyst of ovary", "Germinal epithelial inclusion cyst of ovary", "Germinal inclusion cyst of ovary (disorder)", "benign germinal inclusion cyst of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Germinal inclusion cyst of ovary", "shortest_name_length": 23}
{"curie": "UMLS:C2721654", "names": ["AEFI", "Adverse event following immunization", "Adverse Event Following Immunization", "Adverse event following immunisation", "Adverse event following prior vaccination"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adverse event following immunization", "shortest_name_length": 4}
{"curie": "MONDO:0020741", "names": ["Epd", "EPD", "AASA dehydrogenase deficiency", "pyridoxine-dependent epilepsy", "epilepsy, pyridoxine-dependent", "pyridoxine dependency with seizures", "pyridoxine-dependent epilepsy caused by ALDH7A1 mutant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyridoxine-dependent epilepsy caused by ALDH7A1 mutant", "shortest_name_length": 3}
{"curie": "MONDO:0021379", "names": ["epicardium tumor", "Epicardial Tumor", "epicardial tumor", "epicardial neoplasm", "epicardium neoplasm", "Tumor of Epicardium", "tumor of epicardium", "Epicardial Neoplasm", "Neoplasm of epicardium", "Neoplasm of Epicardium", "neoplasm of epicardium", "Tumor of the Epicardium", "tumor of the epicardium", "Neoplasm of the Epicardium", "neoplasm of the epicardium", "epicardium neoplasm (disease)", "Neoplasm of epicardium (disorder)", "neoplasm of epicardium (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplasm of epicardium", "shortest_name_length": 16}
{"curie": "MONDO:0010890", "names": ["ACFS", "CCGE", "CCGE syndrome", "Acrocardiofacial Syndrome", "ACROCARDIOFACIAL SYNDROME", "acrocardiofacial syndrome", "Acrocardiofacial syndrome", "Acro-cardio-facial syndrome", "ACFS - acrocardiofacial syndrome", "Acrocardiofacial syndrome (disorder)", "CLEFT PALATE, CARDIAC DEFECT, GENITAL ANOMALIES, AND ECTRODACTYLY", "Cleft palate, cardiac defect, genital anomalies, and ectrodactyly", "Cleft Palate, Cardiac Defect, Genital Anomalies, and Ectrodactyly", "cleft palate, CARDIAC defect, genital anomalies, and ectrodactyly", "cleft palate, cardiac defect, genital anomalies, and ectrodactyly", "Cleft palate-cardiac defect-genital anomalies-ectrodactyly syndrome", "cleft palate-cardiac defect-genital anomalies-ectrodactyly syndrome", "CCGE - cleft palate, cardiac defect, genital anomalies, ectrodactyly syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acrocardiofacial syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C1519509", "names": ["Stage II High Grade Burkitt-Like Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II High Grade Burkitt-Like Lymphoma", "shortest_name_length": 41}
{"curie": "UMLS:C2046671", "names": ["Thyroid Gland Hodgkin Lymphoma", "Hodgkin's lymphoma of thyroid gland", "Primary Thyroid Gland Hodgkin Lymphoma", "Hodgkin's lymphoma of thyroid gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's lymphoma of thyroid gland", "shortest_name_length": 30}
{"curie": "MONDO:0003209", "names": ["Thymus adenocarcinoma", "thymus adenocarcinoma", "Thymic Adenocarcinoma", "Thymus Adenocarcinoma", "thymic adenocarcinoma", "adenocarcinoma of Thymus", "Adenocarcinoma of Thymus", "thymus gland adenocarcinoma", "adenocarcinoma of the Thymus", "Adenocarcinoma of the Thymus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thymus gland adenocarcinoma", "shortest_name_length": 21}
{"curie": "MONDO:0019677", "names": ["brachydactyly type E", "type E brachydactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly type E", "shortest_name_length": 20}
{"curie": "MONDO:0012513", "names": ["MODY7", "MODY type 7", "MODY KLF11 related", "diabetes mellitus MODY type 7", "maturity-onset diabetes of the young type 7", "type 7 maturity-onset diabetes of the young", "maturity-onset diabetes of the young, type 7", "MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 7", "Maturity-Onset Diabetes of the Young, Type 7", "Maturity-onset diabetes of the young, type 7", "maturity-onset diabetes of the young - type 7", "maturity-onset diabetes of the young, type VII", "KLF11 maturity-onset diabetes of the young (disease)", "Maturity-onset diabetes of the young, type 7 (disorder)", "MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 7 (disorder)", "maturity-onset diabetes of the young - type 7 (diagnosis)", "maturity-onset diabetes of the young (disease) caused by mutation in KLF11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maturity-onset diabetes of the young type 7", "shortest_name_length": 5}
{"curie": "MONDO:0001116", "names": ["Mesenteric adenitis", "Adenitis;mesenteric", "mesenteric adenitis", "MESENTERIC ADENITIS", "Lymphadenitis;mesenteric", "lymphadenitis mesenteric", "Mesenteric Lymphadenitis", "mesenteric lymphadenitis", "Mesenteric lymphadenitis", "lymphadenitis; mesenteric", "mesenteric; lymphadenitis", "LYMPHADENITIS, MESENTERIC", "Lymphadenitis, Mesenteric", "Mesenteric Lymphadenitides", "Lymphadenitides, Mesenteric", "Mesenteric lymphadenitis, NOS", "Nonspecific mesenteric adenitis", "mesenteric; lymph gland infection", "mesentery lymphadenitis (disease)", "Mesenteric lymphadenitis (disorder)", "mesenteric lymphadenitis (diagnosis)", "nonspecific mesenteric lymphadenitis", "lymphadenitis (disease) of mesentery", "Nonspecific mesenteric lymphadenitis", "Nonspecific mesenteric adenitis (disorder)", "nonspecific mesenteric lymphadenitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mesenteric lymphadenitis", "shortest_name_length": 19}
{"curie": "UMLS:C0948818", "names": ["Catheter site phlebitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Catheter site phlebitis", "shortest_name_length": 23}
{"curie": "UMLS:C0948425", "names": ["Large intestinal bleeding", "Large intestinal hemorrhage", "Large intestinal haemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Large intestinal hemorrhage", "shortest_name_length": 25}
{"curie": "MONDO:0021657", "names": ["stromal tumor ovary", "stromal ovarian tumor", "ovarian stromal tumor", "Ovarian stromal tumor", "ovarian stromal; tumor", "tumor; ovarian stromal", "ovarian stromal tumors", "sex cord stromal tumor", "Stromal tumor of ovary", "stromal tumor of ovary", "Ovarian stromal tumour", "Sex cord tumor of ovary", "Ovarian sex cord tumors", "Stromal tumour of ovary", "Sex cord tumour of ovary", "ovary sex cord-stromal tumor", "ovarian sex-cord stromal tumor", "Ovarian Sex Cord-Stromal Tumor", "ovarian Sex cord-stromal tumor", "Ovarian sex cord-stromal tumor", "ovarian sex cord-stromal tumor", "Sex cord-stromal tumor of ovary", "sex cord-stromal tumor of ovary", "Ovarian sex cord-stromal tumour", "Sex Cord-Stromal Tumor of Ovary", "Ovarian Sex Cord-Stromal Neoplasm", "ovarian Sex cord-stromal neoplasm", "Sex cord-stromal neoplasm of ovary", "Sex cord tumor of ovary (disorder)", "Sex Cord-Stromal Neoplasm of Ovary", "Sex cord-stromal tumor of the ovary", "Sex Cord-Stromal Tumor of the Ovary", "Sex Cord-Stromal Neoplasm of the Ovary", "Sex cord-stromal neoplasm of the ovary", "ovarian sex cord tumor with annular tubules"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian sex cord-stromal tumor", "shortest_name_length": 19}
{"curie": "UMLS:C2347629", "names": ["salivary gland poorly differentiated carcinoma", "poorly differentiated carcinoma, salivary gland", "cancer of the salivary gland, poorly differentiated", "carcinoma of the salivary gland, poorly differentiated", "Poorly Differentiated Salivary Gland Squamous Cell Cancer", "Poorly Differentiated Salivary Gland Squamous Cell Carcinoma", "Salivary Gland Poorly Differentiated Squamous Cell Carcinoma", "Poorly Differentiated Squamous Cell Carcinoma of the Salivary Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Salivary Gland Poorly Differentiated Squamous Cell Carcinoma", "shortest_name_length": 46}
{"curie": "UMLS:C0855156", "names": ["Primary mediastinal large B-cell lymphoma stage II", "Stage II Primary Mediastinal Large B-Cell Lymphoma", "Primary Mediastinal Large B-Cell Lymphoma Stage II", "Stage II Mediastinal (Thymic) Large B-Cell Lymphoma", "Ann Arbor Stage II Primary Mediastinal (Thymic) Large B-Cell Lymphoma", "Large B-cell lymphoma subtype primary mediastinal (Thymic) large B-cell lymphoma stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary mediastinal large B-cell lymphoma stage II", "shortest_name_length": 50}
{"curie": "MONDO:0021485", "names": ["Benign Iris Tumor", "benign iris tumor", "benign iris neoplasm", "Benign Tumor of Iris", "benign tumor of iris", "iris benign neoplasm", "Benign Iris Neoplasm", "Benign tumor of iris", "Benign tumour of iris", "Benign Neoplasm of Iris", "Benign neoplasm of iris", "benign neoplasm of iris", "benign tumor of the iris", "Benign Tumor of the Iris", "Benign Neoplasm of the Iris", "benign neoplasm of the iris", "Benign tumor of iris (disorder)", "benign neoplasm of iris (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of iris", "shortest_name_length": 17}
{"curie": "MONDO:0030890", "names": ["PCH17", "pontocerebellar hypoplasia, IIA 17", "PONTOCEREBELLAR HYPOPLASIA, TYPE 17"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pontocerebellar hypoplasia, IIA 17", "shortest_name_length": 5}
{"curie": "MONDO:0005759", "names": ["Fascioloidosis", "fascioloidiasis", "Fascioloidiases", "Fascioloidiasis", "Infection by Fascioloides", "Infection by Fascioloides, NOS", "Infection caused by Fascioloides", "Infection caused by Fascioloides (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fascioloidiasis", "shortest_name_length": 14}
{"curie": "MONDO:0006082", "names": ["ANSC", "anal cancer squamous cell", "anal squamous cell cancer", "Epidermoid anal carcinoma", "Epidermoid Anal Carcinoma", "Anal Squamous Cell Cancer", "ANAL CANCER SQUAMOUS CELL", "epidermoid anal carcinoma", "squamous cell anal cancer", "anal squamous cell carcinoma", "squamous cell anal carcinoma", "Anal Squamous Cell Carcinoma", "epidermoid carcinoma of anus", "anus squamous cell carcinoma", "Squamous Cell Anal Carcinoma", "Epidermoid Carcinoma of Anus", "Anal squamous cell carcinoma", "Squamous cell carcinoma - anus", "squamous cell carcinoma - anus", "Squamous Cell Carcinoma of Anus", "squamous cell carcinoma of anus", "epidermoid carcinoma of the anus", "Epidermoid Carcinoma of the Anus", "anal cancer, epidermoid carcinoma", "anus cancer, epidermoid carcinoma", "Squamous Cell Carcinoma of the Anus", "squamous cell carcinoma of the anus", "Squamous cell carcinoma of the anus", "anus cancer, squamous cell carcinoma", "anal cancer, squamous cell carcinoma", "squamous cell carcinoma of anus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anal squamous cell carcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0015595", "names": ["pale", "posttransplant acute limbic encephalitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "posttransplant acute limbic encephalitis", "shortest_name_length": 4}
{"curie": "UMLS:C3544060", "names": ["Accidental exposure to product", "Accidental exposures to product"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Accidental exposure to product", "shortest_name_length": 30}
{"curie": "MONDO:0011745", "names": ["Duodenojejunal Atresia, Volvulus, Absent Dorsal Mesentery and Absent Superior Mesenteric Artery", "Duodenojejunal atresia with volvulus, absent dorsal mesentery and absent superior mesenteric artery", "duodenojejunal atresia with volvulus, absent dorsal mesentery and absent superior mesenteric artery", "DUODENOJEJUNAL ATRESIA WITH VOLVULUS, ABSENT DORSAL MESENTERY, AND ABSENT SUPERIOR MESENTERIC ARTERY", "duodenojejunal atresia with volvulus, absent dorsal mesentery, and absent superior mesenteric artery"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "duodenojejunal atresia with volvulus, absent dorsal mesentery, and absent superior mesenteric artery", "shortest_name_length": 95}
{"curie": "UMLS:C1336114", "names": ["stage IA fallopian tube cancer", "Stage IA Fallopian Tube Cancer", "Fallopian Tube Cancer Stage IA", "fallopian tube cancer stage IA", "AJCC stage IA fallopian tube cancer", "AJCC Stage IA Fallopian Tube Cancer", "FIGO stage IA fallopian tube carcinoma", "Stage IA Fallopian Tube Cancer AJCC v6", "Stage IA Fallopian Tube Cancer AJCC v7", "stage IA fallopian tube cancer AJCC v7", "stage IA fallopian tube cancer AJCC v6", "FIGO Stage IA Fallopian Tube Carcinoma", "FIGO stage IA carcinoma of fallopian tube", "FIGO Stage IA Carcinoma of Fallopian Tube", "FIGO Stage IA Carcinoma of the Fallopian Tube", "FIGO stage IA carcinoma of the fallopian tube", "Stage IA Fallopian Tube Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Fallopian Tube Cancer AJCC v6 and v7", "shortest_name_length": 30}
{"curie": "MONDO:0010889", "names": ["ARTERIAL DISSECTION WITH LENTIGINOSIS", "Arterial Dissection with Lentiginosis", "arterial dissection with lentiginosis", "arterial dissection-lentiginosis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arterial dissection-lentiginosis syndrome", "shortest_name_length": 37}
{"curie": "UMLS:C4521785", "names": ["IB", "Stage IB Gastric (Stomach) Cancer", "Pathologic Stage IB Gastric Cancer AJCC v8", "Pathologic Stage IB Gastric Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IB Gastric Cancer AJCC v8", "shortest_name_length": 2}
{"curie": "MONDO:0016976", "names": ["well-differentiated thymic neuroendocrine carcinoma", "Well-differentiated thymic neuroendocrine carcinoma", "Well-differentiated neuroendocrine carcinoma of thymus", "Well-differentiated neuroendocrine carcinoma of thymus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "well-differentiated thymic neuroendocrine carcinoma", "shortest_name_length": 51}
{"curie": "UMLS:C5238466", "names": ["Locally Advanced Midgut Neuroendocrine Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Midgut Neuroendocrine Tumor", "shortest_name_length": 44}
{"curie": "MONDO:0014264", "names": ["OTSC10", "otosclerosis 10", "OTOSCLEROSIS 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "otosclerosis 10", "shortest_name_length": 6}
{"curie": "UMLS:C4330180", "names": ["HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma by AJCC v8 pTNM Stage", "HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma by AJCC v8 Pathologic Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma by AJCC v8 Pathologic Stage", "shortest_name_length": 73}
{"curie": "UMLS:C0744619", "names": ["HEAD NECK CANCER METASTATIC", "Metastatic Head and Neck Cancer", "Head and neck cancer metastatic", "Metastatic Head and Neck Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Head and neck cancer metastatic", "shortest_name_length": 27}
{"curie": "UMLS:C5205931", "names": ["Prostate Follicular Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Follicular Lymphoma", "shortest_name_length": 28}
{"curie": "MONDO:0005853", "names": ["mixed tumor", "mixed neoplasm", "Malignant Mixed Tumor", "Malignant mixed tumor", "malignant mixed tumor", "malignant mixed tumors", "Malignant Mixed Tumors", "mixed tumor, malignant", "Tumor, Malignant Mixed", "Malignant mixed tumour", "mixed cell type cancer", "malignant mixed cancer", "tumor, malignant mixed", "Mixed tumor, malignant", "Mixed Tumor, Malignant", "tumors, malignant mixed", "mixed tumors, malignant", "Mixed tumour, malignant", "tumor, mixed, malignant", "tumor; malignant, mixed", "Tumors, Malignant Mixed", "tumor; mixed, malignant", "TUMOR, MIXED, MALIGNANT", "Mixed Tumors, Malignant", "mixed; tumor, malignant", "Malignant Mixed Neoplasm", "malignant mixed neoplasm", "mixed neoplasm, malignant", "Mixed tumor, malignant NOS", "Mixed tumour, malignant NOS", "Mixed tumor, malignant, NOS", "Mixed tumour, malignant, NOS", "malignant mixed tumor (diagnosis)", "Malignant Salivary Gland Mixed Tumor", "Malignant mixed salivary gland tumor", "Mixed Malignant Salivary Gland Tumor", "Malignant mixed salivary gland tumour", "Cancer of salivary gland, mixed tumor", "Cancer of salivary gland, mixed tumour", "Malignant mixed tumor of salivary gland", "Mixed Malignant Salivary Gland Neoplasm", "malignant mixed tumor of salivary gland", "Malignant Salivary Gland Mixed Neoplasm", "Malignant Mixed Tumor of Salivary Gland", "Mixed Malignant Tumor of Salivary Gland", "Malignant mixed tumour of salivary gland", "Malignant Mixed Neoplasm of Salivary Gland", "Mixed Malignant Neoplasm of Salivary Gland", "Mixed tumor, salivary gland type, malignant", "Malignant Mixed Tumor of the Salivary Gland", "Mixed Malignant Tumor of the Salivary Gland", "Mixed tumour, salivary gland type, malignant", "Mixed Malignant Neoplasm of the Salivary Gland", "Malignant Salivary Gland Mixed Cell Type Tumor", "Malignant Mixed Neoplasm of the Salivary Gland", "salivary gland malignant mixed cell type tumor", "malignant mixed cell type tumor, salivary gland", "salivary gland mixed cell type tumor, malignant", "Mixed tumor, malignant (morphologic abnormality)", "mixed tumor, malignant (morphologic abnormality)", "mixed cell type tumor, salivary gland, malignant", "Malignant Salivary Gland Mixed Cell Type Neoplasm", "Malignant mixed tumor of salivary gland (disorder)", "malignant mixed tumor of salivary gland (diagnosis)", "Malignant Mixed Cell Type Neoplasm of Salivary Gland", "mixed tumor, malignant, NOS (morphologic abnormality)", "Malignant Mixed Cell Type Neoplasm of the Salivary Gland", "cancer of the salivary gland, malignant mixed cell type tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant mixed neoplasm", "shortest_name_length": 11}
{"curie": "MONDO:0000273", "names": ["Kunjin encephalitis", "Kunjin virus infectous disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kunjin virus infectous disease", "shortest_name_length": 19}
{"curie": "MONDO:0017226", "names": ["PMLD", "Pelizaeus-Merzbacher-like disease", "Pelizaeus-Merzbacher-Like disease", "Pelizaeus Merzbacher like disease", "PMLD - Pelizaeus Merzbacher like disease", "Pelizaeus Merzbacher like disease (disorder)", "Pelizaeus-Merzbacher-Like disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pelizaeus-Merzbacher-like disease", "shortest_name_length": 4}
{"curie": "MONDO:0001959", "names": ["labyrinthine bilateral reactive loss", "Bilateral loss of labyrinthine reactivity", "bilateral loss of labyrinthine reactivity", "loss of labyrinthine reactivity, bilateral", "Loss of labyrinthine reactivity, bilateral", "total bilateral loss of labyrinthine reactivity", "total loss of labyrinthine reactivity, bilateral", "total bilateral loss of labyrinthine reactivity (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "labyrinthine bilateral reactive loss", "shortest_name_length": 36}
{"curie": "UMLS:C1258223", "names": ["Flavobacteriaceae Infection", "Infection, Flavobacteriaceae", "Flavobacteriaceae Infections", "Infections, Flavobacteriaceae"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Flavobacteriaceae Infections", "shortest_name_length": 27}
{"curie": "MONDO:0009751", "names": ["atypical hereditary sensory neuropathy", "NEUROPATHY, HEREDITARY SENSORY, ATYPICAL", "Neuropathy, Hereditary Sensory, Atypical", "neuropathy, hereditary sensory, atypical"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuropathy, hereditary sensory, atypical", "shortest_name_length": 38}
{"curie": "MONDO:0003933", "names": ["chest wall bone cancer", "bone cancer of chest wall", "malignant chest wall bone tumor", "Malignant Chest Wall Bone Tumor", "Malignant Bone Tumor of Chest Wall", "malignant bone tumor of chest wall", "malignant chest wall bone neoplasm", "Malignant Chest Wall Bone Neoplasm", "Malignant Bone Neoplasm of Chest Wall", "malignant bone neoplasm of chest wall", "Malignant Bone Tumor of the Chest Wall", "malignant bone tumor of the chest wall", "malignant bone tumor of the Chest Wall", "malignant bone neoplasm of the chest wall", "Malignant Bone Neoplasm of the Chest Wall"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chest wall bone cancer", "shortest_name_length": 22}
{"curie": "MONDO:0700108", "names": ["prion disease, non-human animal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prion disease, non-human animal", "shortest_name_length": 31}
{"curie": "MONDO:0006866", "names": ["Neonatal Myasthenia Gravis", "Neonatal myasthenia gravis", "neonatal myasthenia gravis", "Myasthenia gravis neonatal", "Myasthenia Gravis, Neonatal", "Neonatal myasthenia gravis (disorder)", "neonatal myasthenia gravis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal myasthenia gravis", "shortest_name_length": 26}
{"curie": "UMLS:C1708889", "names": ["Malignant Lung and Pleural Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Lung and Pleural Neoplasm", "shortest_name_length": 35}
{"curie": "MONDO:0030375", "names": ["IMNEPD2", "NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET 2", "neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 2", "shortest_name_length": 7}
{"curie": "MONDO:0001440", "names": ["neurotrophic keratoconjunctivitis", "Neurotrophic keratoconjunctivitis", "neurotrophic; keratoconjunctivitis", "keratoconjunctivitis; neurotrophic", "Neurogenic Keratoconjunctivitis Sicca", "Neurotrophic keratoconjunctivitis (disorder)", "neurotrophic keratoconjunctivitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurotrophic keratoconjunctivitis", "shortest_name_length": 33}
{"curie": "MONDO:0002237", "names": ["carbuncle", "CARBUNCLE", "Carbuncle", "Carbuncles", "carbuncles", "nos carbuncle", "Carbuncle NOS", "Carbuncle (disorder)", "carbuncle (diagnosis)", "carbuncles (physical finding)", "Carbuncle and furuncle of face", "carbuncle and furuncle of foot", "carbuncle and furuncle of neck", "carbuncle and furuncle of hand", "carbuncle and furuncle of face", "carbuncle and furuncle of trunk", "Carbuncle and furuncle of buttock", "carbuncle and furuncle of buttock", "Carbuncle (morphologic abnormality)", "carbuncle and furuncle of gluteal region", "carbuncle and furuncle of leg except foot", "Carbuncle and furuncle of unspecified site", "Carbuncle of skin and subcutaneous tissue, NOS", "carbuncle and furuncle of upper arm and forearm", "carbuncle and furuncle of any part of face except eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carbuncle", "shortest_name_length": 9}
{"curie": "UMLS:C0333186", "names": ["RESTENOSIS", "Restenosis", "restenosis", "Restenosis, NOS", "Restenosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Restenosis", "shortest_name_length": 10}
{"curie": "MONDO:0015041", "names": ["RAEB 2", "RAEB-2", "RAEB II", "RAEB-II", "MDS-EB-2", "refractory anemia with excess blasts-2", "Refractory anemia with excess blasts-2", "Refractory anaemia with excess blasts-2", "Refractory anemia with excess blasts II", "Refractory anaemia with excess blasts II", "Refractory anemia with excess of blasts 2", "Refractory anemia with excess blasts type 2", "refractory anemia with excess blasts type 2", "Myelodysplastic Syndrome with Excess Blasts-2", "Myelodysplastic syndrome with excess blasts-2", "myelodysplastic syndrome with Excess blasts-2", "myelodysplastic syndrome with excess blasts-2", "refractory anemia with excess blasts-2 (diagnosis)", "Myelodysplastic syndrome with excess blasts-2 (disorder)", "MDS-EB-2 - myelodysplastic syndrome with excess blasts-2", "Myelodysplastic syndrome with excess blasts-2 (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myelodysplastic syndrome with excess blasts-2", "shortest_name_length": 6}
{"curie": "MONDO:0054680", "names": ["EDM7", "multiple epiphyseal dysplasia 7", "epiphyseal dysplasia, multiple, 7", "EPIPHYSEAL DYSPLASIA, MULTIPLE, 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epiphyseal dysplasia, multiple, 7", "shortest_name_length": 4}
{"curie": "UMLS:C3272478", "names": ["Ampulla of Vater NET G1", "Ampulla of Vater NET G1 (Carcinoid)", "Carcinoid Tumor of the Ampulla of Vater", "Carcinoid Tumor of the Ampullary Region", "Ampulla of Vater Neuroendocrine Tumor G1", "Neuroendocrine Tumor G1 of the Ampullary Region", "Ampulla of Vater Neuroendocrine Tumor G1 (Carcinoid)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ampulla of Vater Neuroendocrine Tumor G1", "shortest_name_length": 23}
{"curie": "UMLS:C3495947", "names": ["Atypical stress fracture"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypical stress fracture", "shortest_name_length": 24}
{"curie": "MONDO:0001711", "names": ["coma hepaticum", "Gaustad's syndrome", "Hepatoencephalopathy", "hepatic encephalopathy", "ENCEPHALOPATHY HEPATIC", "encephalopathy hepatic", "HEPATIC ENCEPHALOPATHY", "Hepatic encephalopathy", "Encephalopathy hepatic", "Hepatic Encephalopathy", "ENCEPHALOPATHY, HEPATIC", "hepatocerebral syndrome", "hepatic; encephalopathy", "encephalopathy; hepatic", "Encephalopathy, Hepatic", "encephalopathy, hepatic", "Hepatic Encephalopathies", "Encephalopathies, Hepatic", "portacaval encephalopathy", "hepatic coma/encephalopathy", "Hepatic encephalopathy, NOS", "HE - Hepatic encephalopathy", "Portosystemic Encephalopathy", "Portosystemic encephalopathy", "Transient hepatargy syndrome", "encephalopathy portosystemic", "portosystemic encephalopathy", "Hepatocerebral Encephalopathy", "Hepatocerebral encephalopathy", "Encephalopathy, Portosystemic", "portosystemic; encephalopathy", "encephalopathy; portosystemic", "Portal-Systemic Encephalopathy", "portal-systemic encephalopathy", "Portosystemic Encephalopathies", "portal systemic encephalopathy", "Portal-systemic encephalopathy", "Encephalopathy, Hepatocerebral", "Portal systemic encephalopathy", "Portal Systemic Encephalopathy", "Encephalopathies, Portosystemic", "Hepatocerebral Encephalopathies", "Hepatic encephalopathy syndrome", "Encephalopathy, Portal-Systemic", "Encephalopathy, Portal Systemic", "ENCEPHALOPATHY, PORTAL-SYSTEMIC", "Portal-Systemic Encephalopathies", "Encephalopathies, Hepatocerebral", "Hepatic encephalopathy (disorder)", "Encephalopathies, Portal-Systemic", "hepatic encephalopathy (diagnosis)", "Portal systemic encephalopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatic encephalopathy", "shortest_name_length": 14}
{"curie": "UMLS:C0280100", "names": ["tumor solid", "solid tumor", "Solid Tumor", "Solid tumor", "Solid tumour", "Solid Tumour", "solid tumors", "solid tumour", "Solid Neoplasm", "solid neoplasm", "Solid tumor, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Solid Neoplasm", "shortest_name_length": 11}
{"curie": "MONDO:0018675", "names": ["eye IgG4-related disease", "IgG4-related disease of eye", "IgG4-related ophthalmic disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IgG4-related ophthalmic disorder", "shortest_name_length": 24}
{"curie": "UMLS:C3897737", "names": ["Recurrent Sinonasal Inverted Papilloma", "Recurrent Inverted Schneiderian Papilloma", "Recurrent Sinonasal Inverted Schneiderian Papilloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Sinonasal Inverted Papilloma", "shortest_name_length": 38}
{"curie": "UMLS:C0585265", "names": ["Hypoglossal Nerve Palsy", "Hypoglossal nerve palsy", "Cranial Nerve XII Palsy", "Cranial nerve palsy XII", "Palsy, Hypoglossal Nerve", "Hypoglossal Nerve Palsies", "Palsies, Hypoglossal Nerve", "Twelfth Cranial Nerve Palsy", "Twelfth cranial nerve palsy", "Hypoglossal nerve palsy (disorder)", "CRANIAL NERVE PALSY XII HYPOGLOSSAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypoglossal Nerve Palsy", "shortest_name_length": 23}
{"curie": "UMLS:C1167685", "names": ["Infusion site bruising"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infusion site bruising", "shortest_name_length": 22}
{"curie": "MONDO:0015399", "names": ["Cosack syndrome", "Glossopalatine ankylosis", "glossopalatine ankylosis", "Glossopalatine ankylosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glossopalatine ankylosis", "shortest_name_length": 15}
{"curie": "UMLS:C5447137", "names": ["Breast Nodular Fasciitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Nodular Fasciitis", "shortest_name_length": 24}
{"curie": "MONDO:0012198", "names": ["PCWH", "WS4 plus", "PCWH syndrome", "neurologic Waardenburg-Shah syndrome", "Neurologic Waardenburg Shah syndrome", "Neurologic Waardenburg-Shah syndrome", "WAARDENBURG-SHAH SYNDROME, NEUROLOGIC VARIANT", "Waardenburg-Shah Syndrome, Neurologic Variant", "Waardenburg-Shah syndrome, neurologic variant", "Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease", "PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE", "peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease", "Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Hirschsprung disease-Waardenburg syndrome", "Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease", "peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease", "peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Hirschsprung disease-Waardenburg syndrome", "Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease", "PCWH - peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease", "Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PCWH syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0000211", "names": ["ADSD", "Striatal Degeneration, Autosomal Dominant", "striatal degeneration, autosomal dominant", "autosomal dominant striatal neurodegeneration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "striatal degeneration, autosomal dominant", "shortest_name_length": 4}
{"curie": "MONDO:0016165", "names": ["genetic hypoparathyroidism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genetic hypoparathyroidism", "shortest_name_length": 26}
{"curie": "UMLS:C0333885", "names": ["Mild urothelial cell atypia", "Mild Transitional Cell Atypia", "Mild transitional cell atypia", "Mild transitional cell atypia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mild transitional cell atypia", "shortest_name_length": 27}
{"curie": "OMIM:111620", "names": [], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"]}
{"curie": "UMLS:C3805039", "names": ["Graft versus host disease in eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Graft versus host disease in eye", "shortest_name_length": 32}
{"curie": "MONDO:0005652", "names": ["Arterivirus Infection", "Arterivirus Infections", "Infection, Arterivirus", "Infections, Arterivirus", "Arterivirus infectious disease", "Arterivirus disease or disorder", "Arterivirus caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arterivirus infectious disease", "shortest_name_length": 21}
{"curie": "EFO:0005242", "names": ["methamphetamine-induced psychosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "methamphetamine-induced psychosis", "shortest_name_length": 33}
{"curie": "UMLS:C1710417", "names": ["Thyroid Gland Signet Ring Cell Follicular Adenoma", "Thyroid Gland Signet-Ring Cell Follicular Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Signet Ring Cell Follicular Adenoma", "shortest_name_length": 49}
{"curie": "UMLS:C0876994", "names": ["cardiotoxicity", "Cardiotoxicity", "Cardiac Toxicity", "cardiac toxicity", "Cardiotoxicities", "toxicity, cardiac", "Toxicity, Cardiac", "Cardiac Toxicities", "Cardiotoxicity (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiotoxicity", "shortest_name_length": 14}
{"curie": "MONDO:0001376", "names": ["urinary bladder anterior wall cancer", "malignant tumor of anterior wall of bladder", "malignant neoplasm of anterior wall of bladder", "Malignant neoplasm of anterior wall of bladder", "Malignant neoplasm of anterior wall of urinary bladder", "malignant neoplasm of anterior wall of urinary bladder", "malignant neoplasm of anterior wall of bladder (diagnosis)", "Malignant neoplasm of anterior wall of urinary bladder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urinary bladder anterior wall cancer", "shortest_name_length": 36}
{"curie": "UMLS:C5668177", "names": ["Refractory Malignant Leptomeningeal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Malignant Leptomeningeal Neoplasm", "shortest_name_length": 44}
{"curie": "MONDO:0011141", "names": ["MEGAF", "FOLATE LEVEL IN ERYTHROCYTES", "folate level in erythrocytes", "Folate-responsive megaloblastic anemia", "megaloblastic anemia, folate-responsive", "MEGALOBLASTIC ANEMIA, FOLATE-RESPONSIVE", "Megaloblastic anemia, folate-responsive", "Folate-responsive megaloblastic anaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "megaloblastic anemia, folate-responsive", "shortest_name_length": 5}
{"curie": "EFO:0004149", "names": ["neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuropathy", "shortest_name_length": 10}
{"curie": "MONDO:0016390", "names": ["FIH", "familial hypoparathyroidism", "hypoparathyroidism, familial", "hypoparathyroidism familial isolated", "Hypoparathyroidism familial isolated", "Familial isolated hypoparathyroidism", "familial isolated hypoparathyroidism", "hypoparathyroidism, familial isolated", "Hypoparathyroidism, Familial Isolated", "Familial isolated hypoparathyroidism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial hypoparathyroidism", "shortest_name_length": 3}
{"curie": "UMLS:C0009043", "names": ["Closed Dislocation, Multiple and Ill-Defined Sites", "Closed dislocation, multiple and ill-defined sites", "Simple dislocation, multiple and ill-defined sites"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Simple dislocation, multiple and ill-defined sites", "shortest_name_length": 50}
{"curie": "MONDO:0000508", "names": ["syndromic intellectual disability", "syndrome associated with intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic intellectual disability", "shortest_name_length": 33}
{"curie": "MONDO:0016678", "names": ["maternal disease-related embryofetopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maternal disease-related embryofetopathy", "shortest_name_length": 40}
{"curie": "MONDO:0004404", "names": ["Refractory T-Lymphoblastic Leukemia/Lymphoma", "refractory T lymphoblastic leukemia/lymphoma", "Refractory T Lymphoblastic Leukemia/Lymphoma", "refractory precursor T-lymphoblastic lymphoma/leukemia", "precursor T lymphoblastic lymphoma/leukemia refractory", "precursor T-lymphoblastic lymphoma/leukemia refractory", "Precursor T Lymphoblastic Lymphoma/Leukemia Refractory", "Precursor T-lymphoblastic lymphoma/leukemia refractory", "Refractory Precursor T-Lymphoblastic Lymphoma/Leukemia", "Precursor T-lymphoblastic lymphoma/leukaemia refractory"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "refractory precursor T-lymphoblastic lymphoma/leukemia", "shortest_name_length": 44}
{"curie": "UMLS:C5446865", "names": ["Advanced Epithelioid Mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Epithelioid Mesothelioma", "shortest_name_length": 33}
{"curie": "UMLS:C0686477", "names": ["Metastasis to the Retina", "Metastatic Tumor to the Retina", "Metastatic Neoplasm to the Retina", "retinal neoplasm malignant secondary", "Secondary malignant neoplasm of retina", "Metastatic malignant neoplasm to retina", "Metastatic malignant neoplasm of retina", "Metastatic Malignant Neoplasm in the Retina", "Metastatic Malignant Neoplasm to the Retina", "Secondary malignant neoplasm of retina (diagnosis)", "Metastatic malignant neoplasm to retina (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to retina", "shortest_name_length": 24}
{"curie": "MONDO:0017321", "names": ["Pili torti onychodysplasia", "Twisted hair with nail dysplasias", "pili torti-onychodysplasia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pili torti-onychodysplasia syndrome", "shortest_name_length": 26}
{"curie": "MONDO:0010179", "names": ["Irvh", "IRVH", "Right ventricle hypoplasia", "right ventricle hypoplasia", "right ventricular hypoplasia", "Right ventricular hypoplasia", "hypoplasia of the right ventricle", "Hypoplasia of the right ventricle", "Isolated right ventricular hypoplasia", "isolated right ventricular hypoplasia", "right ventricular hypoplasia, isolated", "Right Ventricular Hypoplasia, Isolated", "RIGHT VENTRICULAR HYPOPLASIA, ISOLATED", "Isolated hypoplasia of the right ventricle", "isolated hypoplasia of the right ventricle", "Isolated right ventricular hypoplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated right ventricular hypoplasia", "shortest_name_length": 4}
{"curie": "UMLS:C4763834", "names": ["Metastatic Sarcomatoid Renal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Sarcomatoid Renal Cell Carcinoma", "shortest_name_length": 43}
{"curie": "UMLS:C5446362", "names": ["Advanced Triple-Negative Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Triple-Negative Breast Carcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0022745", "names": ["labrador lung", "Mixed dust pneumoconiosis", "mixed dust pneumoconiosis", "pneumoconiosis due to mixed dust", "pneumoconiosis due to mixed dusts", "Mixed dust pneumoconiosis (disorder)", "pneumoconiosis due to mixed dust (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed dust pneumoconiosis", "shortest_name_length": 13}
{"curie": "UMLS:C5237187", "names": ["Advanced Lung Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Lung Neuroendocrine Neoplasm", "shortest_name_length": 37}
{"curie": "UMLS:C4527148", "names": ["Recurrent Lymphocyte-Rich Classic Hodgkin Lymphoma", "Recurrent Lymphocyte-Rich Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Lymphocyte-Rich Classic Hodgkin Lymphoma", "shortest_name_length": 50}
{"curie": "MONDO:0008461", "names": ["SPLENOMEGALY SYNDROME WITH SPLENIC GERMINAL CENTER HYPOPLASIA AND REDUCED CIRCULATING T HELPER CELLS", "Splenomegaly Syndrome With Splenic Germinal Center Hypoplasia And Reduced Circulating T-Helper Cells", "splenomegaly syndrome with splenic Germinal center hypoplasia and reduced circulating T helper cells"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "splenomegaly syndrome with splenic Germinal center hypoplasia and reduced circulating T helper cells", "shortest_name_length": 100}
{"curie": "MONDO:0100010", "names": ["tendinopathy", "Tendinopathy", "Tendonopathy", "Tendinopathies", "Tendonopathies", "tendon disease", "Disorder tendon", "Tendon disorder", "DISORDER TENDON", "TENDEN DISORDER", "tendon disorder", "TENDON DISORDER", "disorders tendon", "Tendon disorders", "tendon disorders", "disease of tendon", "disorders tendons", "Disorder of tendon", "disorder of tendon", "Tendon disorder NOS", "Tendinous Disorders", "Disorder of tendon, NOS", "tendon disease or disorder", "Disorder of tendon (disorder)", "disease or disorder of tendon", "disorder of tendon (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tendinopathy", "shortest_name_length": 12}
{"curie": "UMLS:C1334634", "names": ["Mature B-Cell Lymphoma", "Mature B-Cell Lymphomas", "Mature B-Cell Non-Hodgkin Lymphoma", "Mature B-Cell Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mature B-Cell Non-Hodgkin Lymphoma", "shortest_name_length": 22}
{"curie": "UMLS:C3897121", "names": ["Recurrent Protoplasmic Astrocytoma", "recurrent childhood protoplasmic astrocytoma", "Recurrent Childhood Protoplasmic Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Protoplasmic Astrocytoma", "shortest_name_length": 34}
{"curie": "MONDO:0010872", "names": ["PDDP", "PAROTID SALIVARY GLANDS, POLYCYSTIC DYSGENETIC DISEASE OF", "parotid salivary glands, polycystic dysgenetic disease of", "parotid salivary glands, polycystic dysgenetic disease OF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parotid salivary glands, polycystic dysgenetic disease of", "shortest_name_length": 4}
{"curie": "UMLS:C1333559", "names": ["FIGO Stage II GTT", "FIGO Stage II Gestational Trophoblastic Tumor", "FIGO Stage II Gestational Trophoblastic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Stage II Gestational Trophoblastic Tumor", "shortest_name_length": 17}
{"curie": "MONDO:0000973", "names": ["external ear lipoma", "External Ear Lipoma", "external Ear lipoma", "Lipoma of External Ear", "lipoma of external ear", "lipoma of external Ear", "lipoma of the external Ear", "Lipoma of the External Ear", "Lipoma of the External ear", "lipoma of the external ear", "external auditory meatus lipoma", "External Auditory Meatus Lipoma", "Lipoma of external auditory meatus", "lipoma of external auditory meatus", "Lipoma of External Auditory Meatus", "Lipoma of the External Auditory Meatus", "lipoma of the external auditory meatus", "Lipoma of external auditory meatus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "external ear lipoma", "shortest_name_length": 19}
{"curie": "UMLS:C4682587", "names": ["Stage IV Uterine Corpus Adenosarcoma", "Stage IV Uterine Corpus Adenosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Uterine Corpus Adenosarcoma AJCC v8", "shortest_name_length": 36}
{"curie": "MONDO:0700026", "names": ["chromosome 22 disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 22 disorder", "shortest_name_length": 22}
{"curie": "MONDO:0010557", "names": ["CHM", "TCD", "Choroideremia", "CHOROIDEREMIA", "choroideremia", "Choroideraemia", "Choroideremias", "choroidal sclerosis", "Choroideremia (disorder)", "choroideremia (diagnosis)", "Tapetochoroidal dystrophy", "progressive choroidal atrophy", "progressive Choroidal Atrophy", "Progressive Choroidal Atrophy", "progressive tapetochoroidal dystrophy", "Progressive Tapetochoroidal Dystrophy", "Dystrophy, Progressive Tapetochoroidal", "TAPETOCHOROIDAL DYSTROPHY, PROGRESSIVE", "Tapetochoroidal Dystrophy, Progressive", "Tapetochoroidal dystrophy, progressive", "Progressive Tapetochoroidal Dystrophies", "Tapetochoroidal Dystrophies, Progressive", "Dystrophies, Progressive Tapetochoroidal", "Choroideremia (degeneration of the choriocapillaris and retinal pigment epithelium and finally retina)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choroideremia", "shortest_name_length": 3}
{"curie": "MONDO:0010286", "names": ["MRXSSD", "Siderius Hamel syndrome", "Siderius-Hamel syndrome", "SIDERIUS-HAMEL SYNDROME", "Siderius-Hamel Syndrome", "X-linked mental retardation Hamel type", "mental retardation X-linked Siderius type", "Mental retardation X-linked Siderius type", "Mental Retardation, X-Linked, Siderius Type", "X-linked intellectual disability Hamel type", "intellectual deficit X-linked Siderius type", "Siderius X-linked mental retardation syndrome", "SIDERIUS X-LINKED MENTAL RETARDATION SYNDROME", "intellectual disability X-linked Siderius type", "X-linked intellectual disability, Siderius type", "Siderius X-linked intellectual disability syndrome", "mental retardation syndrome, X-linked, Siderius type", "MENTAL RETARDATION, X-LINKED, SYNDROMIC, SIDERIUS TYPE", "mental retardation, X-linked, syndromic, Siderius type", "syndromic X-linked intellectual disability Siderius type", "intellectual disability syndrome, X-linked, Siderius type", "intellectual disability, X-linked, syndromic, Siderius type", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SIDERIUS TYPE", "intellectual developmental disorder, X-linked, syndromic, Siderius type, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic X-linked intellectual disability Siderius type", "shortest_name_length": 6}
{"curie": "MONDO:0013096", "names": ["GLM7", "glioma susceptibility 7", "GLIOMA SUSCEPTIBILITY 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glioma susceptibility 7", "shortest_name_length": 4}
{"curie": "UMLS:C1334225", "names": ["Intermediate Vascular Tumor", "Intermediate Vascular Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intermediate Vascular Neoplasm", "shortest_name_length": 27}
{"curie": "MONDO:0013553", "names": ["ICF2", "ICF syndrome 2", "IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 2", "immunodeficiency-centromeric instability-facial anomalies syndrome 2", "immunodeficiency-centromeric instability-Facial anomalies syndrome type 2", "immunodeficiency-centromeric instability-facial anomalies syndrome type 2", "ZBTB24 immunodeficiency-centromeric instability-facial anomalies syndrome", "immunodeficiency-centromeric instability-facial anomalies syndrome caused by mutation in ZBTB24"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency-centromeric instability-facial anomalies syndrome 2", "shortest_name_length": 4}
{"curie": "UMLS:C0278753", "names": ["recurrent mesothelial sarcoma", "mesothelial sarcoma, recurrent", "Relapsed Malignant Mesothelioma", "Mesothelioma Malignant Recurrent", "Mesothelioma malignant recurrent", "Recurrent Malignant Mesothelioma", "recurrent malignant mesothelioma", "malignant mesothelioma, recurrent", "mesothelioma, recurrent malignant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mesothelioma malignant recurrent", "shortest_name_length": 29}
{"curie": "MONDO:0006404", "names": ["Salivary Gland Large Cell Carcinoma", "large cell salivary gland carcinoma", "salivary gland large cell carcinoma", "Large Cell Salivary Gland Carcinoma", "large cell carcinoma of salivary gland", "saliva-secreting gland large cell carcinoma", "large cell carcinoma of salivary gland (diagnosis)", "large cell undifferentiated salivary gland carcinoma", "Large Cell Undifferentiated Salivary Gland Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "salivary gland large cell carcinoma", "shortest_name_length": 35}
{"curie": "MONDO:0003872", "names": ["ovarian papillary cystadenoma", "Ovarian Papillary Cystadenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian papillary cystadenoma", "shortest_name_length": 29}
{"curie": "MONDO:0001510", "names": ["lateral displacement of eye", "Lateral displacement of eye", "lateral displacement of globe", "Lateral displacement of globe", "Displacement (lateral) of globe", "Lateral displacement of eye (disorder)", "Displacement (lateral) of globe (diagnosis)", "exophthalmos displacement (lateral) of globe"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lateral displacement of eye", "shortest_name_length": 27}
{"curie": "MONDO:0008909", "names": ["CDG X", "CDG-X", "CDG-x", "congenital disorder of glycosylation type I/IIX", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE I/IIx", "Congenital Disorder Of Glycosylation, Type I-IIX", "congenital disorder of glycosylation, type i/IIx", "Carbohydrate-deficient glycoprotein syndrome type III", "CDG - Carbohydrate-deficient glycoprotein syndrome type III", "Carbohydrate-deficient glycoprotein syndrome type III (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital disorder of glycosylation, type i/IIx", "shortest_name_length": 5}
{"curie": "MONDO:0024569", "names": ["OPA8", "optic atrophy 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "optic atrophy 8", "shortest_name_length": 4}
{"curie": "MONDO:0007476", "names": ["DUPC1", "plantar fibromas", "PLANTAR FIBROMAS", "Plantar Fibromas", "Dupuytren contracture", "DUPUYTREN CONTRACTURE 1", "Dupuytren contracture 1", "Dupuytren Contracture 1", "PLANTAR FIBROMATOSIS, FAMILIAL", "familial Dupuytren contracture", "plantar fibromatosis, familial", "Plantar Fibromatosis, Familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial Dupuytren contracture", "shortest_name_length": 5}
{"curie": "MONDO:0014455", "names": ["CAGSSS", "CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURAL HEARING LOSS, AND SKELETAL DYSPLASIA", "Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome", "cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome", "cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia", "Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome", "CAGSSS - cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome", "Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0011351", "names": ["DFNB21", "autosomal recessive deafness 21", "deafness, autosomal recessive 21", "DEAFNESS, AUTOSOMAL RECESSIVE 21", "Deafness, Autosomal Recessive 21", "deafness, autosomal recessive type 21", "autosomal recessive nonsyndromic deafness 21", "tecta autosomal recessive nonsyndromic deafness", "TECTA autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 21", "autosomal recessive nonsyndromic deafness type 21", "autosomal recessive nonsyndromic deafness caused by mutation in TECTA", "autosomal recessive nonsyndromic deafness caused by mutation in tecta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 21", "shortest_name_length": 6}
{"curie": "MONDO:0020400", "names": ["congenital supravalvular mitral ring"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital supravalvular mitral ring", "shortest_name_length": 36}
{"curie": "MONDO:0013634", "names": ["HSN2C", "hereditary sensory neuropathy type 2C", "hereditary sensory neuropathy type IIC", "neuropathy, hereditary sensory, type 2C", "neuropathy, hereditary sensory, type IIC", "NEUROPATHY, HEREDITARY SENSORY, TYPE IIC", "KIF1A hereditary sensory and autonomic neuropathy type 2", "hereditary sensory and autonomic neuropathy type 2 caused by mutation in KIF1A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuropathy, hereditary sensory, type 2C", "shortest_name_length": 5}
{"curie": "UMLS:C0857112", "names": ["eye glaucoma", "glaucoma eye", "eyes glaucoma", "glaucoma both eyes", "Bilateral glaucoma", "Glaucoma both eyes", "Bilateral Glaucoma", "glaucoma in both eyes", "Glaucoma of both eyes", "Bilateral glaucoma (disorder)", "glaucoma in both eyes (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bilateral glaucoma", "shortest_name_length": 12}
{"curie": "MONDO:0002676", "names": ["Fibrosarcoma", "fibrosarcoma", "Adult Fibrosarcoma", "adult fibrosarcoma", "fibrosarcoma, adult", "sarcoma, fibro-, adult", "Fibrosarcoma - not infantile", "adult fibrosarcoma (disease)", "fibrosarcoma (disease) of adults", "Fibrosarcoma (excluding infantile fibrosarcoma)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult fibrosarcoma", "shortest_name_length": 12}
{"curie": "UMLS:C4725077", "names": ["Locally Advanced Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Melanoma", "shortest_name_length": 25}
{"curie": "UMLS:C4682565", "names": ["Stage IVB Uterine Corpus Leiomyosarcoma", "Stage IVB Uterine Corpus Leiomyosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Uterine Corpus Leiomyosarcoma AJCC v8", "shortest_name_length": 39}
{"curie": "UMLS:C1266002", "names": ["Non-small cell carcinoma", "non-small cell carcinoma", "Non-Small Cell Carcinoma", "small cell carcinoma non", "non small cell carcinoma", "Non-small cell carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-small cell carcinoma", "shortest_name_length": 24}
{"curie": "UMLS:C0339114", "names": ["rodent ulcer eyelid", "Rodent ulcer of eyelid", "Ocular Basal Cell Carcinoma", "Eyelid Basal Cell Carcinoma", "cell carcinoma basal eyelid", "basal cell carcinoma eyelid", "Basal cell carcinoma of eyelid", "basal cell carcinoma of eyelid", "skin neoplasm eyelid basal cell", "Basal cell carcinoma of eyelid (disorder)", "basal cell carcinoma of eyelid (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Basal cell carcinoma of eyelid", "shortest_name_length": 19}
{"curie": "UMLS:C4288051", "names": ["Uterine Corpus Endometrial Stromal and Related Tumors", "Uterine Corpus Endometrial Stromal and Related Neoplasms"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Corpus Endometrial Stromal and Related Neoplasms", "shortest_name_length": 53}
{"curie": "MONDO:0014450", "names": ["BNAH2", "BREAST AND/OR NIPPLES, APLASIA OR HYPOPLASIA OF, 2", "BREASTS AND/OR NIPPLES, APLASIA OR HYPOPLASIA OF, 2", "PTPRF isolated congenital breast hypoplasia/aplasia", "breasts and/or nipples, aplasia or hypoplasia of, 2", "breasts and/or nipples, aplasia or hypoplasia of, type 2", "isolated congenital breast hypoplasia/aplasia caused by mutation in PTPRF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breasts and/or nipples, aplasia or hypoplasia of, 2", "shortest_name_length": 5}
{"curie": "UMLS:C1336143", "names": ["Stage IB Retinoblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Retinoblastoma", "shortest_name_length": 23}
{"curie": "UMLS:C3272832", "names": ["Colorectal Leiomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Leiomyosarcoma", "shortest_name_length": 25}
{"curie": "MONDO:0005133", "names": ["Endo", "ENDOMETRIOSIS", "endometriosis", "endometrioses", "ENDOMETRIOSES", "Endometriosis", "Endometrioses", "Endometriosis, NOS", "Sigmoid endometriosis", "endometriosis (disease)", "Endometriosis (disorder)", "Endometriosis (clinical)", "endometriosis (diagnosis)", "Endometriosis, unspecified", "Endometriosis, site unspecified", "displacement of the endometrial tissue", "Endometriosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometriosis", "shortest_name_length": 4}
{"curie": "UMLS:C2985171", "names": ["Glioneuronal Tumor with Neuropil-Like Islands"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Glioneuronal Tumor with Neuropil-Like Islands", "shortest_name_length": 45}
{"curie": "MONDO:0001852", "names": ["Small Bowel Lymphoma", "small bowel lymphoma", "lymphoma of small bowel", "Lymphoma of small bowel", "Lymphoma of Small Bowel", "small intestine lymphoma", "Small Intestine Lymphoma", "intestine lymphoma small", "lymphoma small intestine", "small intestinal Lymphoma", "SMALL INTESTINAL LYMPHOMA", "Small Intestinal Lymphoma", "small intestinal lymphoma", "lymphoma, small intestine", "Lymphoma of Small Intestine", "lymphoma of small intestine", "lymphoma of the small bowel", "Lymphoma of small intestine", "Lymphoma of the Small Bowel", "lymphoma of the small intestine", "Lymphoma of the Small Intestine", "Primary Small Intestinal Lymphoma", "primary small intestinal lymphoma", "malignant lymphoma of small intestine", "Lymphoma of small intestine (disorder)", "malignant lymphoma of small intestine (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small intestine lymphoma", "shortest_name_length": 20}
{"curie": "UMLS:C0920211", "names": ["Paternal drugs affecting fetus", "Paternal drugs affecting foetus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paternal drugs affecting fetus", "shortest_name_length": 30}
{"curie": "MONDO:0003057", "names": ["meningioma", "Meningioma", "Childhood Meningioma", "Pediatric Meningioma", "childhood meningioma", "pediatric meningioma", "meningioma, childhood", "childhood meningioma (disease)", "pediatric meningioma (disease)", "meningioma (disease) of childhood", "Brain tumor, child: Meningioma/Meningeal tumors", "pediatric central nervous system tumor, meningioma", "childhood central nervous system tumor, meningioma", "central nervous system tumor, childhood meningioma", "central nervous system tumor, meningioma, childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pediatric meningioma", "shortest_name_length": 10}
{"curie": "UMLS:C3897527", "names": ["Stage IIIC Esophageal Cancer", "Stage IIIC Esophageal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Esophageal Cancer AJCC v7", "shortest_name_length": 28}
{"curie": "MONDO:0013531", "names": ["PSPHD", "PSPH deficiency", "Deficiency of choline phosphatase", "PHOSPHOSERINE PHOSPHATASE DEFICIENCY", "phosphoserine phosphatase deficiency", "Phosphoserine phosphatase deficiency", "3-phosphoserine phosphatase deficiency", "Deficiency of phosphoserine phosphatase", "PSPH deficiency, infantile/juvenile form", "Deficiency of phosphoserine phosphatase (disorder)", "3-phosphoserine phosphatase deficiency, infantile/juvenile form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PSPH deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C1333177", "names": ["CLD", "Lymphoproliferative Disorder of Skin", "Cutaneous Lymphoproliferative Disorder", "Lymphoproliferative Disorder of the Skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoproliferative Disorder of the Skin", "shortest_name_length": 3}
{"curie": "MONDO:0007286", "names": ["CTRCT30", "cataract 30", "CATARACT 30", "Dusty cataract", "cataract type 30", "cataract Coppock-like", "cataract 30 pulverulent", "cataract 30, pulverulent", "cataract 30, multiple types", "CATARACT 30, MULTIPLE TYPES", "Cataract, Nuclear Diffuse Nonprogressive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 30", "shortest_name_length": 7}
{"curie": "MONDO:0022986", "names": ["DIPNECH", "DIP-NECH", "diffuse idiopathic pulmonary neuroendocrine cell hyperplasia", "Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia", "Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diffuse idiopathic pulmonary neuroendocrine cell hyperplasia", "shortest_name_length": 7}
{"curie": "MONDO:0008269", "names": ["PPD1", "Extra thumb", "extra; thumb", "accessory thumb", "Fromont Anomaly", "Fromont anomaly", "FROMONT ANOMALY", "Accessory thumb", "thumb; accessory", "accessory; thumb", "thenar hypoplasia", "Thumb polydactyly", "THUMB POLYDACTYLY", "thumb polydactyly", "Accessory thumb(s)", "thumb; polydactyly", "polydactyly; thumb", "Supernumerary thumb", "Polydactyly of thumb", "thumb; supernumerary", "POLYDACTYLY, PREAXIAL", "preaxial polydactyly 1", "polydactyly preaxial 1", "POLYDACTYLY, PREAXIAL I", "polydactyly, preaxial 1", "Polydactyly, Preaxial I", "polydactyly, preaxial I", "Preaxial hand polydactyly", "preaxial polydactyly hands", "preaxial polydactyly type 1", "Preaxial polydactyly type 1", "Polydactyly preaxial type 1", "accessory thumb (diagnosis)", "polydactyly, preaxial type 1", "Preaxial polydactyly of hands", "preaxial polydactyly of hands", "Polydactyly affecting the thumb", "Polydactyly of a biphalangeal thumb", "polydactyly of a biphalangeal thumb", "congenital hand deformity accessory thumb", "preaxial polydactyly hands (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polydactyly of a biphalangeal thumb", "shortest_name_length": 4}
{"curie": "MONDO:0002010", "names": ["FGS", "FGS1", "fg syndrome", "FG syndrome", "Keller syndrome", "Opitz-Kaveggia syndrome", "mental retardation, large head, imperforate anus, congenital hypotonia, and partial agenesis of corpus callosum", "intellectual disability, large head, imperforate anus, congenital hypotonia, and partial agenesis of corpus callosum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FG syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0014992", "names": ["LIS8", "lissencephaly 8", "LISSENCEPHALY 8", "lissencephaly type 8", "lissencephaly 8; LIS8", "TMTC3 lissencephaly (disease)", "lissencephaly (disease) caused by mutation in TMTC3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lissencephaly 8", "shortest_name_length": 4}
{"curie": "MONDO:0100165", "names": ["PDMI", "PNDM1", "permanent neonatal diabetes mellitus 1", "diabetes mellitus, permanent neonatal 1", "diabetes mellitus, permanent, of infancy", "DIABETES MELLITUS, PERMANENT, OF INFANCY", "DIABETES MELLITUS, PERMANENT NEONATAL, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "permanent neonatal diabetes mellitus 1", "shortest_name_length": 4}
{"curie": "MONDO:0012863", "names": ["ADHD6", "DIGIT SPAN QUANTITATIVE TRAIT LOCUS", "digit span quantitative trait locus", "attention deficit-hyperactivity disorder, susceptibility to, 6", "ATTENTION DEFICIT-HYPERACTIVITY DISORDER, SUSCEPTIBILITY TO, 6", "attention Deficit-hyperactivity disorder, susceptibility to, type 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "attention deficit-hyperactivity disorder, susceptibility to, 6", "shortest_name_length": 5}
{"curie": "MONDO:0019013", "names": ["angioneurotic edema", "non-histaminic angioedema", "bradykinine-induced angioedema", "non histamine-induced angioedema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-histaminic angioedema", "shortest_name_length": 19}
{"curie": "MONDO:0008960", "names": ["Charcot-Marie-Tooth disease and deafness", "CHARCOT-MARIE-TOOTH DISEASE AND DEAFNESS", "DEAFNESS WITH CHARCOT-MARIE-TOOTH DISEASE", "Deafness with Charcot-Marie-Tooth Disease", "deafness with Charcot-Marie-Tooth disease", "Charcot-Marie-tooth disease-deafness-intellectual disability syndrome", "Charcot-Marie-Tooth disease-hearing loss-intellectual disability syndrome", "Neuropathy, Hereditary Motor and Sensory, with Deafness, Mental Retardation, and Absent Sensory Large Myelinated Fibers", "NEUROPATHY, HEREDITARY MOTOR AND SENSORY, WITH DEAFNESS, MENTAL RETARDATION, AND ABSENT SENSORY LARGE MYELINATED FIBERS", "neuropathy, hereditary motor and sensory, with deafness, mental retardation, and absent sensory large myelinated fibers", "hereditary motor and sensory neuropathy with deafness, intellectual disability and absent sensory large myelinated fibers", "neuropathy, hereditary motor and sensory, with deafness, intellectual disability, and absent sensory large myelinated fibers"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease-hearing loss-intellectual disability syndrome", "shortest_name_length": 40}
{"curie": "MONDO:0010948", "names": ["CCZS", "CTRCT10", "cataract 10 multiple types", "cataract 10, multiple types", "CATARACT 10, MULTIPLE TYPES", "CRYBA1 early-onset non-syndromic cataract", "congenital zonular cataract with sutural opacities", "CATARACT, CONGENITAL ZONULAR, WITH SUTURAL OPACITIES", "Cataract, Congenital Zonular, with Sutural Opacities", "cataract, congenital zonular, with sutural opacities", "early-onset non-syndromic cataract caused by mutation in CRYBA1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 10 multiple types", "shortest_name_length": 4}
{"curie": "UMLS:C4682570", "names": ["Stage II Uterine Corpus Endometrial Stromal Sarcoma", "Stage II Uterine Corpus Endometrial Stromal Sarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Uterine Corpus Endometrial Stromal Sarcoma AJCC v8", "shortest_name_length": 51}
{"curie": "UMLS:C0340161", "names": ["hemomediastinum", "Hemomediastinum", "Haemomediastinum", "Hematomediastinum", "Haematomediastinum", "mediastinal hematoma", "MEDIASTINAL HEMATOMA", "Mediastinal hematoma", "Mediastinal haematoma", "Hematomediastinum (disorder)", "mediastinal hematoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hematomediastinum", "shortest_name_length": 15}
{"curie": "MONDO:0020732", "names": ["progeria", "Progeria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progeria", "shortest_name_length": 8}
{"curie": "UMLS:C1332253", "names": ["Ampulla of Vater Tubulovillous Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ampulla of Vater Tubulovillous Adenoma", "shortest_name_length": 38}
{"curie": "MONDO:0035151", "names": ["Del(17)(q24)", "17q24.2 microdeletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "17q24.2 microdeletion syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0020830", "names": ["diaphragmitis", "Diaphragmitis", "diaphragmatitis", "Diaphragmatitis", "Diaphragmitis (disorder)", "diaphragmitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diaphragmitis", "shortest_name_length": 13}
{"curie": "MONDO:0010172", "names": ["VACTERL-H", "VACTERL-H, X-Linked", "VACTERL hydrocephaly", "Sujansky-Leonard syndrome", "VACTERL with hydrocephalus", "X-linked VACTERL-H syndrome", "VATER ASSOCIATION WITH HYDROCEPHALUS", "Vater Association With Hydrocephalus", "Vater association with hydrocephalus", "VACTERL association with hydrocephaly", "VACTERL ASSOCIATION WITH HYDROCEPHALUS", "VACTERL Association With Hydrocephalus", "VACTERL association with hydrocephalus", "VACTERL association with hydrocephaly, X-linked", "VACTERL Association With Hydrocephalus, X-Linked", "Vater association with macrocephaly and ventriculomegaly", "VATER ASSOCIATION WITH MACROCEPHALY AND VENTRICULOMEGALY", "Vater Association With Macrocephaly And Ventriculomegaly", "vertebral (V), anal (A), cardiac (C), tracheoesophageal (te), renal (R) and limb (L) anomalies and hydrocephaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "VACTERL with hydrocephalus", "shortest_name_length": 9}
{"curie": "MONDO:0021202", "names": ["allergic otitis media", "Allergic otitis media", "Otitis media, allergic", "otitis; media, allergic", "Allergic otitis media NOS", "allergic otitis media (disease)", "Allergic otitis media (disorder)", "allergic otitis media (diagnosis)", "allergic nonsuppurative otitis media", "allergic form of otitis media (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "allergic otitis media", "shortest_name_length": 21}
{"curie": "MONDO:0025138", "names": ["VES", "swine vesicular exanthema", "Swine Vesicular Exanthema", "swine vesicular Exanthemas", "Swine Vesicular Exanthemas", "vesicular exanthema of swine", "Vesicular Exanthema of Swine", "Vesicular exanthema of swine", "Vesicular exanthema of swine (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vesicular exanthema of swine", "shortest_name_length": 3}
{"curie": "MONDO:0003947", "names": ["Hyper IgM", "Hyper IgM Syndrome", "hyper igm syndrome", "hyper IgM syndrome", "Hyper IgM syndrome", "hyper-IgM syndrome", "Hyper-IgM Syndrome", "Hyper-IgM Syndromes", "Hyperimmunoglobulin M syndrome", "hyperimmunoglobulin m syndrome", "hyperimmunoglobulin M syndrome", "Hyperimmunoglobulin M Syndrome", "immunodeficiency with hyper-IgM", "Immunodeficiency with Hyper-IgM", "Hyper-IgM Immunodeficiency Syndrome", "Hyper IgM Immunodeficiency Syndrome", "Syndrome, Hyper-IgM Immunodeficiency", "Hyper-IgM Immunodeficiency Syndromes", "Immunodeficiency Syndrome, Hyper-IgM", "Immunodeficiency Syndromes, Hyper-IgM", "Syndromes, Hyper-IgM Immunodeficiency", "Immunodeficiency with Hyper-IgM Syndrome", "Immunodeficiency with Hyper IgM Syndrome", "Hyperimmunoglobulin M syndrome (disorder)", "Hyperimmunoglobulin M syndrome (diagnosis)", "Immunodeficiency with IgM hypergammaglobulinemia", "Immunodeficiency with IgM hypergammaglobulinaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyper-IgM syndrome", "shortest_name_length": 9}
{"curie": "MONDO:0008236", "names": ["PHLEBECTASIA OF LIPS", "phlebectasia of lips", "Phlebectasia Of Lips"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phlebectasia of lips", "shortest_name_length": 20}
{"curie": "MONDO:0032799", "names": ["MTDPS16", "mitochondrial DNA depletion syndrome 16", "mitochondrial DNA depletion syndrome 16 (hepatic type)", "MITOCHONDRIAL DNA DEPLETION SYNDROME 16 (HEPATIC TYPE)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial DNA depletion syndrome 16 (hepatic type)", "shortest_name_length": 7}
{"curie": "UMLS:C1518006", "names": ["Low-Grade Papillary Urothelial Carcinoma", "Bladder Non-Invasive Papillary Urothelial Carcinoma, Low Grade", "Non-Invasive Bladder Papillary Urothelial Carcinoma, Low Grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder Non-Invasive Papillary Urothelial Carcinoma, Low Grade", "shortest_name_length": 40}
{"curie": "MONDO:0044209", "names": ["complement activation, lectin pathway disease", "disorder of lectin complement activation pathway", "disorder of complement activation, lectin pathway"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of lectin complement activation pathway", "shortest_name_length": 45}
{"curie": "MONDO:0012896", "names": ["PSORS10", "psoriasis 10", "psoriasis susceptibility 10", "psoriasis 10, susceptibility to", "PSORIASIS 10, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "psoriasis 10, susceptibility to", "shortest_name_length": 7}
{"curie": "MONDO:0060489", "names": ["SRXX4", "46,XX SEX reversal 4", "46,XX SEX REVERSAL 4", "46,XX sex reversal 4", "46, XX sex reversal 4", "46,XX SEX REVERSAL, SRY-NEGATIVE", "46,XX Sex reversal, Sry-Negative"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XX sex reversal 4", "shortest_name_length": 5}
{"curie": "MONDO:0010040", "names": ["ataxia, spastic, childhood-onset, autosomal recessive, with optic atrophy and mental retardation", "ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTIC ATROPHY AND MENTAL RETARDATION", "ataxia, spastic, childhood-onset, autosomal recessive, with optic atrophy and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ataxia, spastic, childhood-onset, autosomal recessive, with optic atrophy and intellectual disability", "shortest_name_length": 96}
{"curie": "UMLS:C1708671", "names": ["Leaflet Disruption Due To Unknown Cause"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leaflet Disruption Due To Unknown Cause", "shortest_name_length": 39}
{"curie": "MONDO:0020927", "names": ["postaxial polydactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postaxial polydactyly", "shortest_name_length": 21}
{"curie": "UMLS:C1302836", "names": ["Lipomatous hamartoma", "Lipomatous Hamartoma", "Lipomatous hamartoma (disorder)", "Lipomatous hamartoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lipomatous hamartoma", "shortest_name_length": 20}
{"curie": "UMLS:C5419394", "names": ["Fetal Harm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fetal Harm", "shortest_name_length": 10}
{"curie": "MONDO:0009255", "names": ["GALK", "GALAC2", "GALK-D", "galactosemia 2", "Galactosemia 2", "GALK DEFICIENCY", "galactosemia II", "GALK Deficiency", "Galactosemia 2s", "Galk deficiency", "GALK deficiency", "Galactosemia II", "GALACTOSEMIA II", "Deficiency, GALK", "Galactosaemia II", "GALK Deficiencies", "Deficiencies, GALK", "Galactosemia Type 2", "galactosemia type 2", "Galactosemia type 2", "type ii galactosemia", "Galactosemia, type II", "Galactokinase Deficiency", "GALACTOKINASE DEFICIENCY", "galactokinase deficiency", "Galactokinase deficiency", "galactokinase; deficiency", "deficiency; galactokinase", "Deficiency, Galactokinase", "Galactokinase Deficiencies", "Deficiencies, Galactokinase", "Deficiency of galactokinase", "GALK - Galactokinase deficiency", "Galactokinase Deficiency Disease", "Galactokinase Deficiency Diseases", "Galactokinase deficiency syndrome", "Deficiency Disease, Galactokinase", "Hereditary Galactokinase Deficiency", "hereditary galactokinase deficiency", "Deficiency, Hereditary Galactokinase", "Galactokinase Deficiency, Hereditary", "Hereditary Galactokinase Deficiencies", "galactokinase deficiency galactosemia", "Galactokinase deficiency galactosemia", "Galactokinase deficiency galactosaemia", "Deficiency of galactokinase (disorder)", "Galactokinase Deficiencies, Hereditary", "Deficiencies, Hereditary Galactokinase", "Galactosemia - galactokinase deficiency", "galactokinase deficiency with cataracts", "Galactosaemia - galactokinase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "galactokinase deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0003027", "names": ["thyroid angiosarcoma", "Thyroid Angiosarcoma", "thyroid hemangiosarcoma", "angiosarcoma of thyroid", "Angiosarcoma of Thyroid", "Thyroid Hemangiosarcoma", "Thyroid Gland Angiosarcoma", "hemangiosarcoma of thyroid", "Hemangiosarcoma of Thyroid", "thyroid gland angiosarcoma", "Angiosarcoma of the Thyroid", "angiosarcoma of the thyroid", "thyroid gland hemangiosarcoma", "angiosarcoma of thyroid gland", "Thyroid Gland Hemangiosarcoma", "Angiosarcoma of Thyroid Gland", "Hemangiosarcoma of the Thyroid", "hemangiosarcoma of the thyroid", "hemangiosarcoma of the Thyroid", "hemangiosarcoma of thyroid gland", "Hemangiosarcoma of Thyroid Gland", "Angiosarcoma of the Thyroid Gland", "angiosarcoma of the thyroid gland", "MESOTHELIOMA, ATRIOCAVAL, MALIGNANT", "thyroid gland angiosarcoma (disease)", "hemangiosarcoma of the thyroid gland", "Hemangiosarcoma of the Thyroid Gland", "angiosarcoma (disease) of thyroid gland", "Thyroid Gland Malignant Hemangioendothelioma", "thyroid gland malignant hemangioendothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid gland angiosarcoma", "shortest_name_length": 20}
{"curie": "MONDO:0008007", "names": ["Tooth ankylosis", "tooth ankylosis", "Teeth Ankyloses", "Tooth Ankyloses", "Teeth Ankylosis", "Ankylosed teeth", "Tooth Ankylosis", "ankylosis; teeth", "Dental Ankyloses", "Dental ankylosis", "DENTAL ANKYLOSIS", "Ankyloses, Tooth", "Dental Ankylosis", "teeth; ankylosis", "dental ankylosis", "Ankylosis, Tooth", "Ankylosis, Dental", "Ankyloses, Dental", "ankylosis of tooth", "Ankylosis of tooth", "ankylosis of teeth", "Ankylosis of teeth", "ANKYLOSIS OF TEETH", "Ankylosis of Teeth", "molar 1 reinclusion", "molar I reinclusion", "MOLAR I REINCLUSION", "Dentoalveolar Ankyloses", "Dentoalveolar Ankylosis", "Ankylosis, Dentoalveolar", "Ankyloses, Dentoalveolar", "Ankylosis of tooth (disorder)", "ankylosis of teeth (diagnosis)", "calcareous tooth ankylosis (disease)", "ankylosis (disease) of calcareous tooth", "secondary retention of permanent molars", "permanent molars, secondary retention OF", "PERMANENT MOLARS, SECONDARY RETENTION OF", "abnormal fusion of dental cementum with alveolar bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tooth ankylosis", "shortest_name_length": 15}
{"curie": "MONDO:0013555", "names": ["HPS3", "Hermansky-Pudlak syndrome 3", "HERMANSKY-PUDLAK SYNDROME 3", "HPS3 Hermansky-Pudlak syndrome", "Hermansky-Pudlak syndrome type 3", "Hermansky-Pudlak syndrome caused by mutation in HPS3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hermansky-Pudlak syndrome 3", "shortest_name_length": 4}
{"curie": "UMLS:C3272798", "names": ["GCHP", "Colorectal GCHP", "Colorectal Goblet Cell Rich Hyperplastic Polyp"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Goblet Cell Rich Hyperplastic Polyp", "shortest_name_length": 4}
{"curie": "UMLS:C5420845", "names": ["Reactive Hyperplasia of the Retinal Pigment Epithelium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reactive Hyperplasia of the Retinal Pigment Epithelium", "shortest_name_length": 54}
{"curie": "MONDO:0003563", "names": ["Diffuse Pulmonary Fibrosis", "diffuse pulmonary fibrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diffuse pulmonary fibrosis", "shortest_name_length": 26}
{"curie": "MONDO:0003753", "names": ["Nasal Vestibule Papilloma", "nasal vestibule papilloma", "papilloma of nasal vestibule", "Papilloma of Nasal Vestibule", "Papilloma of nasal vestibule", "Viral wart of nasal vestibule", "Papilloma of the Nasal Vestibule", "papilloma of the nasal vestibule", "nasal vestibule squamous papilloma", "Nasal Vestibule Squamous Papilloma", "Squamous Papilloma of Nasal Vestibule", "squamous papilloma of nasal vestibule", "Nasal Vestibule Squamous Cell Papilloma", "Papilloma of nasal vestibule (disorder)", "squamous papilloma of the nasal Vestibule", "squamous papilloma of the nasal vestibule", "Squamous Papilloma of the Nasal Vestibule"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasal vestibule squamous papilloma", "shortest_name_length": 25}
{"curie": "MONDO:0016426", "names": ["fusariosis", "Fusarioses", "Fusariosis", "infection fusarium", "Fusarium infection", "fusarium infection", "Fusarium Infection", "fusarium; infection", "FUSARIUM INFECTIONS", "infection; fusarium", "Fusarium Infections", "Infection, Fusarium", "Infections, Fusarium", "Fusarium infection, NOS", "Fusarium infectious disease", "Fusarium disease or disorder", "Fusarium infection (disorder)", "Fusarium caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fusariosis", "shortest_name_length": 10}
{"curie": "UMLS:C0274053", "names": ["Burn of axilla", "Burn of Axilla", "burns of axilla", "Burn of axilla, NOS", "Burn of axilla (disorder)", "burns of axilla (diagnosis)", "Burn of unspecified degree of axilla"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Burn of axilla", "shortest_name_length": 14}
{"curie": "UMLS:C1335478", "names": ["Cerebral Lymphoma in Immunocompetent Host", "Primary Cerebral Lymphoma in Immunocompetent Host"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebral Lymphoma in Immunocompetent Host", "shortest_name_length": 41}
{"curie": "MONDO:0017974", "names": ["46,XY DSD induced by maternal-exposure to endocrine disruptors", "46,XY disorder of sex development induced by maternal-exposure to endocrine disruptors"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XY disorder of sex development induced by maternal-exposure to endocrine disruptors", "shortest_name_length": 62}
{"curie": "MONDO:0013501", "names": ["ALS14", "FTDALS6", "ALS14, FORMERLY", "ALS14 (diagnosis)", "amyotrophic lateral sclerosis 14", "VCP amyotrophic lateral sclerosis", "amyotrophic lateral sclerosis ALS14", "amyotrophic lateral sclerosis type 14", "amyotrophic lateral sclerosis caused by mutation in VCP", "frontotemporal dementia and/or amyotrophic lateral sclerosis-6", "FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 6", "frontotemporal dementia and/or amyotrophic lateral sclerosis 6", "amyotrophic lateral sclerosis, with or without frontotemporal dementia", "Amyotrophic Lateral Sclerosis 14, With or Without Frontotemporal Dementia", "AMYOTROPHIC LATERAL SCLEROSIS 14 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA, FORMERLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontotemporal dementia and/or amyotrophic lateral sclerosis 6", "shortest_name_length": 5}
{"curie": "MONDO:0015217", "names": ["isolated developmental defect of the eye", "nonsyndromic developmental defect of the eye", "non-syndromic developmental defect of the eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-syndromic developmental defect of the eye", "shortest_name_length": 40}
{"curie": "MONDO:0012173", "names": ["LCHADD", "LCHAD Deficiency", "LCHAD deficiency", "LCHAD DEFICIENCY", "fatty liver, acute, of pregnancy", "HELLP syndrome, maternal, of pregnancy", "trifunctional protein deficiency type 1", "Trifunctional Protein Deficiency, Type 1", "long-chain 3-OH acyl-CoA dehydrogenase deficiency", "Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency", "Long chain 3 hydroxyacyl coA dehydrogenase deficiency", "long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency", "long chain 3-hydroxyacyl-CoA dehydrogenase deficiency", "3-hydroxyacyl-CoA dehydrogenase long chain deficiency", "Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency", "LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY", "long-chain 3-hydroxy acyl CoA dehydrogenase deficiency", "Long-chain 3-hydroxy-acyl-CoA dehydrogenase deficiency", "Deficiency of long-chain 3-hydroxyacyl-CoA dehydrogenase", "Long-Chain 3-Hydroxyacyl-Coenzyme A Dehydrogenase Deficiency", "Long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency", "Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency", "long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency", "Long chain 3-hydroxyacyl CoA dehydrogenase deficiency (LCHAD)", "LCHADD - long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency", "Long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "long chain 3-hydroxyacyl-CoA dehydrogenase deficiency", "shortest_name_length": 6}
{"curie": "MONDO:0021510", "names": ["Benign Prostate Tumor", "benign prostate tumor", "Benign prostatic tumor", "Benign prostatic tumour", "benign prostate neoplasm", "Benign Tumor of Prostate", "PROSTATE NEOPLASM BENIGN", "Benign tumor of prostate", "benign tumor of prostate", "Neoplasm benign;prostate", "Benign Prostate Neoplasm", "Benign Prostatic Neoplasm", "Benign tumour of prostate", "benign prostatic neoplasm", "Prostatic neoplasms benign", "Benign neoplasm of prostate", "Benign Neoplasm of Prostate", "benign neoplasm of prostate", "Benign Tumor of the Prostate", "benign tumor of the prostate", "Benign prostatic neoplasm NOS", "prostate gland benign neoplasm", "benign tumor of prostate gland", "Benign Neoplasm of the Prostate", "benign neoplasm of the prostate", "benign neoplasm of prostate gland", "Benign neoplasm of prostate (disorder)", "benign neoplasm of prostate gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of prostate", "shortest_name_length": 21}
{"curie": "UMLS:C0271662", "names": ["GDM, class A1", "Gestational Diabetes Mellitus, A1", "Gestational diabetes mellitus class A1", "Gestational diabetes mellitus, class A1", "Gestational Diabetes, A1 White Classification", "Gestational diabetes mellitus class A1 (disorder)", "Gestational Diabetes Mellitus, A1 White Classification", "gestational diabetes mellitus, White's classification A1", "gestational diabetes mellitus, White's classification A1 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gestational diabetes mellitus class A1", "shortest_name_length": 13}
{"curie": "MONDO:0030077", "names": ["VCRL3", "CONGENITAL NAD DEFICIENCY DISORDER 3", "Congenital Nad Deficiency Disorder 3", "vertebral, cardiac, renal, and limb defects syndrome 3", "VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vertebral, cardiac, renal, and limb defects syndrome 3", "shortest_name_length": 5}
{"curie": "UMLS:C0862226", "names": ["stage IV mycosis fungoides/Sezary syndrome", "Mycosis fungoides/Sezary syndrome stage IV", "mycosis fungoides/Sezary syndrome, stage IV", "Stage IV Mycosis Fungoides and Sezary Syndrome", "Stage IV Mycosis Fungoides and Sézary Syndrome", "stage IV mycosis fungoides and the Sezary syndrome", "Stage IV Mycosis Fungoides and Sézary Syndrome AJCC v7", "Stage IV Mycosis Fungoides and Sezary Syndrome AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mycosis fungoides/Sezary syndrome stage IV", "shortest_name_length": 42}
{"curie": "MONDO:0013194", "names": ["PSEUDOPILI ANNULATI", "Pseudopili annulati"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pseudopili annulati", "shortest_name_length": 19}
{"curie": "MONDO:0013983", "names": ["HED", "EDA", "ECTD11B", "ectodermal dysplasia 11B", "ECTODERMAL DYSPLASIA, ANHIDROTIC", "ectodermal dysplasia, anhidrotic", "ECTODERMAL DYSPLASIA, HYPOHIDROTIC", "ectodermal dysplasia, hypohidrotic", "ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive", "ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive", "shortest_name_length": 3}
{"curie": "MONDO:0016834", "names": ["dup(16)(p11.2p12.2)", "Dup(16)(p11.2p12.2)", "Trisomy 16p11.2p12.2", "trisomy 16p11.2p12.2", "16p11.2 microduplication syndrome", "16p11.2p12.2 microduplication syndrome", "16p11.2-p12.2 microduplication syndrome", "16p11.2p12.2 microduplication syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "16p11.2p12.2 microduplication syndrome", "shortest_name_length": 19}
{"curie": "MONDO:0013685", "names": ["PNCA4", "BRCA1 familial pancreatic carcinoma", "susceptibility to pancreatic cancer 4", "PANCREATIC CANCER, SUSCEPTIBILITY TO, 4", "pancreatic cancer, susceptibility to, 4", "pancreatic cancer, susceptibility to, type 4", "familial pancreatic carcinoma caused by mutation in BRCA1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic cancer, susceptibility to, 4", "shortest_name_length": 5}
{"curie": "UMLS:C5401308", "names": ["Advanced Biliary Tract Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Biliary Tract Carcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C1336710", "names": ["Testicular Germ Cell Neoplasia In Situ with Extratubular Extension", "Testicular Intratubular Germ Cell Neoplasia with Extratubular Extension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular Germ Cell Neoplasia In Situ with Extratubular Extension", "shortest_name_length": 66}
{"curie": "UMLS:C5447985", "names": ["Breast Classic Lobular Carcinoma In Situ Type B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Classic Lobular Carcinoma In Situ Type B", "shortest_name_length": 47}
{"curie": "MONDO:0019017", "names": ["short fifth metacarpals-insulin resistance syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short fifth metacarpals-insulin resistance syndrome", "shortest_name_length": 51}
{"curie": "UMLS:C2981365", "names": ["Stage IIIC Gastric Cancer", "Stage IIIC Gastric Cancer AJCC v7", "Stage IIIC Gastric (Stomach) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Gastric Cancer AJCC v7", "shortest_name_length": 25}
{"curie": "MONDO:0007767", "names": ["HRPT1", "hyperparathyroidism 1", "HYPERPARATHYROIDISM 1", "Hyperparathyroidism 1", "hyperparathyroidism type 1", "parathyroid adenoma, familial", "hyperparathyroidism, familial primary", "hyperparathyroidism, familial isolated primary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperparathyroidism 1", "shortest_name_length": 5}
{"curie": "UMLS:C5419746", "names": ["Refractory Kidney Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Kidney Carcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0030929", "names": ["MCPH27", "microcephaly 27, primary, autosomal dominant", "MICROCEPHALY 27, PRIMARY, AUTOSOMAL DOMINANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly 27, primary, autosomal dominant", "shortest_name_length": 6}
{"curie": "MONDO:0002519", "names": ["Ulcer anal", "anal ulcer", "Anal ulcer", "Anal Ulcer", "ANAL ULCER", "ulcer; anus", "Anal Ulcers", "anus; ulcer", "anal ulcers", "Ulcer, Anal", "ANAL FISSURE", "Anal Fissure", "Anal erosion", "Ulcers, Anal", "anal fissure", "disease anus", "Fissure;anal", "Fissure anal", "anus disease", "Anal fissure", "anal disease", "Anus Disease", "DISORDER ANUS", "Anal Disorder", "Anus Diseases", "anal disorder", "ulcer of anus", "Anal disorder", "Anus disorder", "disorder anus", "anal fissures", "Fissure, Anal", "fissure; anus", "anus diseases", "Disorder anus", "ANUS, FISSURE", "anus disorder", "ANUS DISORDER", "Disease, Anus", "Anal fissures", "anus; fissure", "Ulcer of anus", "anus disorders", "anus; disorder", "Anus--Diseases", "fissure-in-ano", "Anal Disorders", "Diseases, Anus", "FISSURE IN ANO", "Fissure in ano", "anal disorders", "Fissure in Ano", "Fissure-in-ano", "fissure in ano", "disease of anus", "ANAL ULCERATION", "disorder of anus", "Disorder of anus", "Anal disorder NOS", "single anal ulcer", "anal ulcer single", "Ulceration of anus", "Anal mucosal ulcer", "Anal disorder, NOS", "anal ulcer (___ cm)", "solitary anal ulcer", "Solitary anal ulcer", "Disease of anus, NOS", "single ulcer of anus", "Solitary ulcer of anus", "anal ulcer (diagnosis)", "Disorder of anal region", "disorder of anal region", "Anal fissure (disorder)", "Ulcer of anus (disorder)", "anal fissure (diagnosis)", "anal fissure and fistula", "anus disease or disorder", "Anal fissure, unspecified", "nontraumatic tear of anus", "Nontraumatic tear of anus", "Tear of anus, nontraumatic", "anal ulcer single (___ cm)", "disease (or disorder); anus", "Disorder of anus (disorder)", "disease or disorder of anus", "disorder of anus (diagnosis)", "single anal ulcer (diagnosis)", "ulcer of anus (physical finding)", "Disorder of anal region (disorder)", "disorder of anal region (diagnosis)", "single ulcer of anus (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anus disorder", "shortest_name_length": 10}
{"curie": "UMLS:C0434579", "names": ["closed shoulder dislocation", "Closed Dislocation of Shoulder", "Simple dislocation of shoulder", "closed dislocation of shoulder", "Closed dislocation of shoulder", "Closed dislocation of humerus, NOS", "Closed dislocation of shoulder, NOS", "Closed traumatic shoulder dislocation", "shoulder dislocation closed traumatic", "Closed dislocation of shoulder region", "closed dislocation of shoulder (diagnosis)", "shoulder region dislocation traumatic closed", "shoulder dislocation closed traumatic (diagnosis)", "Closed dislocation of shoulder region (diagnosis)", "closed traumatic dislocation of glenohumeral joint", "Closed traumatic dislocation of glenohumeral joint", "Closed traumatic dislocation of joint of shoulder region", "Closed traumatic dislocation of glenohumeral joint (disorder)", "closed traumatic dislocation of glenohumeral joint (diagnosis)", "Closed traumatic dislocation of joint of shoulder region (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Closed traumatic dislocation of glenohumeral joint", "shortest_name_length": 27}
{"curie": "UMLS:C5418953", "names": ["Refractory Ovarian Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Ovarian Serous Adenocarcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0008689", "names": ["DHS", "DHS1", "PSHK1", "xerocytosis, hereditary", "Desiccytosis, hereditary", "PSEUDOHYPERKALEMIA EDINBURGH", "pseudohyperkalemia Edinburgh", "pseudohyperkalemia edinburgh", "dehydrated hereditary stomatocytosis", "dehydrated hereditary stomatocytosis 1", "pseudohyperkalemia familial 1, due to red cell leak", "PSEUDOHYPERKALEMIA, FAMILIAL, 1, DUE TO RED CELL LEAK", "pseudohyperkalemia, familial, 1, due to Red cell leak", "Dehydrated hereditary stomatocytosis pseudohyperkalemia and perinatal edema", "DEHYDRATED hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema", "dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema", "dehydrated hereditary stomatocytosis 1 with or without pseudohyperkalemia and/or perinatal edema", "Dehydrated hereditary stomatocytosis 1 with or without pseudohyperkalemia and/Or perinatal edema", "DEHYDRATED HEREDITARY STOMATOCYTOSIS 1 WITH OR WITHOUT PSEUDOHYPERKALEMIA AND/OR PERINATAL EDEMA", "DEHYDRATED hereditary stomatocytosis 1 with or without pseudohyperkalemia and/OR perinatal edema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema", "shortest_name_length": 3}
{"curie": "UMLS:C1516073", "names": ["Astler-Coller C2 Rectal Carcinoma", "Astler-Coller C2 Carcinoma of Rectum", "Astler-Coller C2 Carcinoma of the Rectum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Astler-Coller C2 Rectal Carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0100383", "names": ["AML, t(11;19)(q23;p13)", "acute myeloid leukemia, t(11;19)(q23;p13)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, t(11;19)(q23;p13)", "shortest_name_length": 22}
{"curie": "MONDO:0700103", "names": ["nutritional deficiency disease, non-human animal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nutritional deficiency disease, non-human animal", "shortest_name_length": 48}
{"curie": "MONDO:0004302", "names": ["Chief cell adenoma", "Chief Cell Adenoma", "chief cell adenoma", "chief cell; adenoma", "adenoma; chief cell", "parathyroid chief cell adenoma", "Parathyroid chief cell adenoma", "Parathyroid Chief Cell Adenoma", "PARATHYROID ADENOMA CHIEF CELL", "chief cell adenoma of parathyroid", "Chief Cell Adenoma of Parathyroid", "parathyroid gland chief cell adenoma", "Parathyroid Gland Chief Cell Adenoma", "chief cell adenoma of the parathyroid", "Chief Cell Adenoma of the Parathyroid", "chief cell adenoma of parathyroid gland", "Chief cell adenoma of Parathyroid gland", "Chief Cell Adenoma of Parathyroid Gland", "Chief Cell Adenoma of the Parathyroid Gland", "chief cell adenoma of the parathyroid gland", "Chief cell adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chief cell adenoma", "shortest_name_length": 18}
{"curie": "MONDO:0011850", "names": ["Mgr5", "MGR5", "migraine with or without aura, susceptibility to, 5", "MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 5", "migraine with or without aura, susceptibility to, type 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "migraine with or without aura, susceptibility to, 5", "shortest_name_length": 4}
{"curie": "MONDO:0019395", "names": ["HS", "HAS", "Hinman Syndrome", "Hinman syndrome", "Hinman-Allen syndrome", "occult neuropathic bladder", "Occult neuropathic bladder", "non-neurogenic neurogenic bladder", "Non-neurogenic neurogenic bladder", "Non-Neurogenic Neurogenic Bladder", "Nonneurogenic neurogenic bladder dysfunction", "Nonneurogenic neurogenic bladder dysfunction (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hinman syndrome", "shortest_name_length": 2}
{"curie": "MONDO:0005318", "names": ["Aphtha", "aphtha", "aphthae", "Aphthae", "Aphthosis", "Canker sore", "CANKER SORE", "canker sore", "Canker Sore", "oral aphthae", "Sore, Canker", "canker sores", "Canker Sores", "Oral aphthae", "Sores, Canker", "cankers sores", "oral; aphthae", "aphthae; oral", "ulcer; aphthae", "aphthous ulcer", "Aphthous ulcer", "Aphthous Ulcer", "APHTHOUS ULCER", "Ulcer;aphthous", "aphthae; ulcer", "Ulcer aphthous", "ulcer; aphthous", "aphthous ulcers", "Ulcer, Aphthous", "Aphthous ulcers", "Aphthous Ulcers", "aphthous; ulcer", "Ulcer, aphthous", "Ulcers, Aphthous", "CANKER SORES ORAL", "Oral aphthae, NOS", "oral canker sores", "Canker sores oral", "Oral aphthous ulcer", "aphthous stomatitis", "Aphthous Stomatitis", "stomatitis; aphthae", "Ulcer aphthous oral", "APHTHOUS STOMATITIS", "Aphthous ulceration", "Stomatitis aphthous", "oral aphthous ulcer", "aphthous ulceration", "ULCER APHTHOUS ORAL", "STOMATITIS APHHNOUS", "Aphthous stomatitis", "ORAL ULCER APHTHOUS", "STOMATITIS APHTHOUS", "aphthae; stomatitis", "Ulcers aphthous oral", "Stomatitis, Aphthous", "aphthous; stomatitis", "stomatitis; aphthous", "oral aphthous ulcers", "STOMATITIS, APHTHOUS", "aphthous ulcerations", "aphthous oral ulcers", "ULCERS APHTHOUS ORAL", "recurrent canker sore", "Aphthous Stomatitides", "recurrent mouth ulcer", "Recurrent oral aphthae", "Buccal aphthous ulcers", "Stomatitides, Aphthous", "Recurrent canker sores", "recurrent mouth ulcers", "Aphthous ulcer of mouth", "recurrent aphthous ulcer", "Recurrent aphthous ulcer", "Aphthous ulcer recurrent", "APHTHOUS ULCER RECURRENT", "Ulcerative stomatitis NOS", "Recurrent aphthous ulcers", "aphthous ulcer (diagnosis)", "Recurrent aphthous ulceration", "recurrent aphthous stomatitis", "Recurrent aphthous stomatitis", "Recurrent ulcerative stomatitis", "Aphtha (morphologic abnormality)", "Aphthous ulcer of mouth (disorder)", "Recurrent aphthous ulcer (disorder)", "RAS - Recurrent aphthous stomatitis", "recurrent aphthous ulcer (diagnosis)", "Recurrent aphthous stomatitis (disorder)", "Aphthous ulceration of skin and/or mucous membrane", "Aphthous ulceration of skin and/or mucous membrane (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canker sore", "shortest_name_length": 6}
{"curie": "UMLS:C0347023", "names": ["thyroid metastases", "metastases thyroid", "thyroid metastasis", "metastasis to thyroid", "Metastases to thyroid", "Metastasis to thyroid", "Metastasis to the Thyroid", "Cancer metastatic to thyroid", "Metastasis to the Thyroid Gland", "Metastatic Tumor to the Thyroid", "metastasis to thyroid (diagnosis)", "Metastatic Neoplasm to the Thyroid", "thyroid malignant neoplasm secondary", "Metastatic Tumor to the Thyroid Gland", "Secondary malignant neoplasm of thyroid", "Secondary Malignant Tumor to the Thyroid", "Metastatic Neoplasm to the Thyroid Gland", "Metastatic Malignant Tumor to the Thyroid", "Secondary Malignant Neoplasm to the Thyroid", "Metastatic Malignant Neoplasm to the Thyroid", "secondary malignant neoplasm of thyroid gland", "Secondary malignant neoplasm of thyroid gland", "Metastatic malignant neoplasm to thyroid gland", "Metastatic malignant neoplasm of thyroid gland", "Secondary Malignant Tumor to the Thyroid Gland", "Metastatic Malignant Tumor to the Thyroid Gland", "Secondary Malignant Neoplasm to the Thyroid Gland", "Metastatic Malignant Neoplasm to the Thyroid Gland", "Metastatic Malignant Neoplasm in the Thyroid Gland", "Metastatic malignant neoplasm to thyroid gland (disorder)", "Secondary malignant neoplasm of thyroid gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Malignant Neoplasm to the Thyroid", "shortest_name_length": 18}
{"curie": "UMLS:C2064465", "names": ["Salivary Gland Sebaceous Carcinoma", "sebaceous carcinoma of salivary gland", "Salivary Gland Sebaceous Adenocarcinoma", "sebaceous carcinoma of salivary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sebaceous carcinoma of salivary gland", "shortest_name_length": 34}
{"curie": "UMLS:C0864946", "names": ["Malignant Fundus Neoplasm", "Malignant neoplasm of fundus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Fundus Neoplasm", "shortest_name_length": 25}
{"curie": "MONDO:0007307", "names": ["HMSN1", "CMT1B", "CMT 1B", "HMSN1B", "HMSN 1B", "HMSN IB", "peroneal muscular atrophy", "Charcot Marie Tooth disease type 1B", "Charcot-Marie-Tooth disease type 1B", "Charcot-Marie-Tooth disease Type 1B", "Charcot-Marie-Tooth Disease Type 1B", "Charcot Marie Tooth Disease, Type IB", "Charcot Marie Tooth Disease, Type 1B", "Charcot-Marie-Tooth disease, type 1B", "CHARCOT-MARIE-TOOTH DISEASE, TYPE 1B", "Charcot-Marie-Tooth disease, type IB", "Charcot-Marie-Tooth Disease, Type IB", "Charcot-Marie-Tooth Disease, Type Ib", "Charcot-Marie-Tooth Disease, Type 1B", "Charcot-Marie-Tooth neuropathy type 1B", "MPZ Charcot-Marie-Tooth disease type 1", "Charcot Marie Tooth Neuropathy, Type 1B", "Charcot-Marie-Tooth neuropathy, type 1B", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 1B", "Charcot-Marie-Tooth Neuropathy, Type 1B", "hereditary motor and sensory neuropathy 1", "hereditary motor and sensory neuropathy IB", "HEREDITARY MOTOR AND SENSORY NEUROPATHY IB", "hereditary motor and sensory neuropathy 1B", "Hereditary Motor And Sensory Neuropathy IB", "Hereditary Motor and Sensory Neuropathy 1B", "Charcot-Marie-Tooth disease, type IB (disorder)", "Charcot-Marie-Tooth disease Type 1B (diagnosis)", "Charcot-Marie-Tooth Disease, Demyelinating, Type 1B", "Charcot-Marie-Tooth disease, demyelinating, type 1B", "CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B", "Charcot-Marie-Tooth disease type 1 caused by mutation in MPZ", "Charcot-Marie-Tooth disease slow nerve conduction type linked to Duffy", "Charcot-Marie-Tooth Disease, Slow Nerve Conduction Type, Linked To Duffy", "Charcot-Marie-Tooth disease, slow nerve conduction type, linked to Duffy", "CHARCOT-MARIE-TOOTH DISEASE, SLOW NERVE CONDUCTION TYPE, LINKED TO DUFFY", "autosomal dominant Charcot-Marie-Tooth disease with focally folded myelin sheaths type 1B", "CHARCOT-MARIE-TOOTH DISEASE, AUTOSOMAL DOMINANT, WITH FOCALLY FOLDED MYELIN SHEATHS, TYPE 1B", "Charcot-Marie-Tooth disease, autosomal dominant, with focally folded myelin sheaths, type 1B", "Charcot-Marie-Tooth Disease, Autosomal Dominant, with Focally Folded Myelin Sheaths, Type 1B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 1B", "shortest_name_length": 5}
{"curie": "MONDO:0017713", "names": ["disorder of fatty acid oxidation and ketogenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of fatty acid oxidation and ketogenesis", "shortest_name_length": 48}
{"curie": "MONDO:0002044", "names": ["spastic ectropion", "Spastic ectropion", "Spastic ectropion (disorder)", "spastic ectropion (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic ectropion", "shortest_name_length": 17}
{"curie": "UMLS:C4521804", "names": ["Stage IIIA Anal Cancer", "Stage IIIA Anal Cancer AJCC v8", "Stage IIIA Anal Carcinoma AJCC v8", "Stage IIIA Anal Canal and Perianal (Anal Margin) Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Anal Cancer AJCC v8", "shortest_name_length": 22}
{"curie": "UMLS:C4055374", "names": ["Bone Epithelioid Hemangioendothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone Epithelioid Hemangioendothelioma", "shortest_name_length": 37}
{"curie": "MONDO:0013675", "names": ["MMDS2", "BOLA3 deficiency", "BOLA3 (bolA family member 3) deficiency", "multiple mitochondrial dysfunctions syndrome 2", "Multiple mitochondrial dysfunctions syndrome type 2", "multiple mitochondrial dysfunctions syndrome type 2", "BOLA3 fatal multiple mitochondrial dysfunctions syndrome", "MMDS2 - multiple mitochondrial dysfunctions syndrome type 2", "Multiple mitochondrial dysfunctions syndrome type 2 (disorder)", "MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 WITH HYPERGLYCINEMIA", "multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia", "fatal multiple mitochondrial dysfunctions syndrome caused by mutation in BOLA3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple mitochondrial dysfunctions syndrome 2", "shortest_name_length": 5}
{"curie": "MONDO:0010180", "names": ["SCDO1", "Jarcho-Levin syndrome", "costovertebral dysplasia", "autosomal recessive spondylocostal dysostosis", "spondylocostal dysostosis, autosomal recessive", "Spondylocostal dysostosis, autosomal recessive", "spondylocostal dysostosis 1, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive spondylocostal dysostosis", "shortest_name_length": 5}
{"curie": "UMLS:C0848383", "names": ["ulcer eye", "Eye ulcer", "Ulcer;eye", "eye ulcer", "eye ulcers", "eyes ulcers"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eye ulcer", "shortest_name_length": 9}
{"curie": "MONDO:0002158", "names": ["Tubal cancer", "tubal cancer", "malignant tubal tumor", "cancer fallopian tube", "Malignant tubal tumor", "fallopian tube cancer", "cancer fallopian tubes", "fallopian tubes cancer", "fallopian tube neoplasm", "cancer of fallopian tube", "cancer of fallopian tubes", "Cancer of fallopian tubes", "neoplasm of fallopian tube", "tumor of the fallopian tube", "cancer of the fallopian tube", "Malignant neoplasm of oviduct", "Fallopian Tube Malignant Tumor", "Malignant Fallopian Tube Tumor", "malignant fallopian tube tumor", "fallopian tube malignant tumor", "Tumor, Fallopian Tube, Malignant", "tumor, fallopian tube, malignant", "fallopian tube malignant neoplasm", "Malignant tumor of fallopian tube", "malignant fallopian tube neoplasm", "malignant tumor of fallopian tube", "Malignant Tumor of Fallopian Tube", "Malignant Fallopian Tube Neoplasm", "Fallopian Tube Malignant Neoplasm", "malignant neoplasm of uterine tube", "malignant tumor of fallopian tubes", "malignant tumour of fallopian tube", "Malignant tumor of fallopian tubes", "Malignant neoplasm of uterine tube", "Fallopian tube neoplasms malignant", "Malignant tumour of fallopian tube", "neoplasm, fallopian tube, malignant", "Neoplasm, Fallopian Tube, Malignant", "malignant neoplasm of fallopian tube", "Malignant neoplasm of fallopian tube", "Malignant Neoplasm of Fallopian Tube", "malignant tumor of the fallopian tube", "Malignant Tumor of the Fallopian Tube", "malignant neoplasm of the fallopian tube", "Malignant Neoplasm of the Fallopian Tube", "Malignant neoplasm of fallopian tube NOS", "Malignant tumor of fallopian tube (disorder)", "malignant neoplasm of fallopian tube (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fallopian tube cancer", "shortest_name_length": 12}
{"curie": "UMLS:C2204343", "names": ["Salivary Gland Non-Hodgkin Lymphoma", "non-Hodgkin's lymphoma of salivary gland", "Primary Salivary Gland Non-Hodgkin Lymphoma", "non-Hodgkin's lymphoma of salivary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-Hodgkin's lymphoma of salivary gland", "shortest_name_length": 35}
{"curie": "UMLS:C0205204", "names": ["scab", "Scab", "crust", "scabs", "Crust", "CRUST", "crusts", "scabbed", "Scabbed", "crusting", "Scabbing", "scabbing", "scab (symptom)", "Cutaneous Crust", "Crust (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Scab", "shortest_name_length": 4}
{"curie": "MONDO:0007818", "names": ["HIES1", "AD-HIES", "HIE syndrome", "JOB syndrome", "hie syndrome", "Job Syndrome", "job syndrome", "Job syndrome", "syndrome job", "HIE Syndrome", "JOB SYNDROME", "Jobs Syndrome", "Syndrome, Job", "HIE Syndromes", "jobs syndrome", "Job Syndromes", "job's syndrome", "Job's Syndrome", "Syndromes, Job", "Job's syndrome", "STAT3 Deficiency", "Buckley syndrome", "Buckley Syndrome", "STAT3 deficiency", "Buckley Syndromes", "hyper-ige syndrome", "Quie-Hill syndrome", "Hyper IgE Syndrome", "Hyper-IgE Syndrome", "Hyper-IgE syndrome", "hyper ige syndrome", "Hyper IgE syndrome", "Buckley's syndrome", "Hyper-IgE Syndromes", "Job-Buckley Syndrome", "Job-Buckley syndrome", "job-buckley syndrome", "Job Buckley Syndrome", "Job-Buckley Syndromes", "HIES autosomal dominant", "Autosomal Dominant HIES", "autosomal dominant HIES", "Autosomal dominant HIES", "Autosomal Dominant HIESs", "HIES, AUTOSOMAL DOMINANT", "HIES, autosomal dominant", "HIES, Autosomal Dominant", "HIESs, Autosomal Dominant", "Job's syndrome (disorder)", "Job's syndrome (diagnosis)", "Hyperimmunoglobulin E syndrome", "Hyperimmunoglobulin E Syndrome", "hyperimmunoglobulin E syndrome", "hyperimmunoglobulin e syndrome", "hyperimmunoglobulin E; syndrome", "Job syndrome autosomal dominant", "syndrome; hyperimmunoglobulin E", "AD hyperimmunoglobulin E syndrome", "Hyperimmunoglobulinemia E Syndrome", "Hyperimmunoglobulinemia E Syndromes", "Hyperimmunoglobulin E [IgE] syndrome", "autosomal dominant hyper IgE syndrome", "Autosomal dominant hyper-IgE syndrome", "hyperimmunoglobulin E syndrome type 1", "autosomal dominant hyper-IgE syndrome", "Hyperimmunoglobulin E syndrome type 1", "hyper-IgE recurrent infection syndrome", "Hyper IgE Syndrome, Autosomal Dominant", "hyper-IgE syndrome, autosomal dominant", "Hyper-IgE Recurrent Infection Syndrome", "Hyper-IgE Syndrome, Autosomal Dominant", "HYPER-IgE SYNDROME, AUTOSOMAL DOMINANT", "hyper Ig E syndrome, autosomal dominant", "Recurring cold staphylococcal abscesses", "hyper IgE recurrent infection syndrome 1", "hyperimmunoglobulin E syndrome (diagnosis)", "autosomal dominant hyperimmunoglobulin E syndrome", "Autosomal dominant hyperimmunoglobulin E syndrome", "Hyperimmunoglobulin E-Recurrent Infection Syndrome", "Hyperimmunoglobulin E-recurrent infection syndrome", "Hyperimmunoglobulin E Recurrent Infection Syndrome", "hyperimmunoglobulin E-recurrent infection syndrome", "Hyperimmunoglobulin E, Recurrent Infection Syndrome", "Hyper Immunoglobulin E Syndrome, Autosomal Dominant", "Hyper-Immunoglobulin E Syndrome, Autosomal Dominant", "DERMATITIS, ATOPIC, WITH IMPAIRED NEUTROPHIL CHEMOTAXIS", "Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant", "hyper-IgE recurrent infection syndrome, autosomal dominant", "HYPER-IgE RECURRENT INFECTION SYNDROME 1, AUTOSOMAL DOMINANT", "hyper-IgE recurrent infection syndrome 1, autosomal dominant", "hyperimmunoglobulin E recurrent infection syndrome, autosomal dominant", "Immunodeficiency with Defective Leukocyte and Lymphocyte Function and with Response to Histamine-1 Antagonist", "immunodeficiency with defective leukocyte and lymphocyte function and with response to histamine-1 antagonist"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyper-IgE recurrent infection syndrome 1, autosomal dominant", "shortest_name_length": 5}
{"curie": "UMLS:C0542269", "names": ["nqmi", "nqwmi", "non q-wave myocardial infarction", "non q wave myocardial infarction", "non-q wave myocardial infarction", "infarction myocardial non q wave", "Non-Q wave myocardial infarction", "MYOCARDIAL INFARCTION NON Q WAVE", "Non-Q wave myocardial infarction NOS", "acute non-Q-wave myocardial infarction", "Non-Q wave myocardial infarction (disorder)", "acute non-Q-wave myocardial infarction (diagnosis)", "subendocardial non-Q-wave myocardial infarction acute"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Q wave myocardial infarction", "shortest_name_length": 4}
{"curie": "UMLS:C4285809", "names": ["Contraindicated product administered"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Contraindicated product administered", "shortest_name_length": 36}
{"curie": "MONDO:0014134", "names": ["PPH2", "PULMONARY HYPERTENSION, PRIMARY, 2", "pulmonary hypertension, primary, 2", "SMAD9 primary pulmonary hypertension", "pulmonary hypertension, primary, type 2", "primary pulmonary hypertension caused by mutation in SMAD9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary hypertension, primary, 2", "shortest_name_length": 4}
{"curie": "UMLS:C0029560", "names": ["Other conjunctivitis", "Other and unspecified conjunctivitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Other conjunctivitis", "shortest_name_length": 20}
{"curie": "MONDO:0015935", "names": ["extragonadal germinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extragonadal germinoma", "shortest_name_length": 22}
{"curie": "UMLS:C4683575", "names": ["Lugano Classification Limited Stage Adult Non-Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Limited Stage Adult Non-Hodgkin Lymphoma AJCC v8", "shortest_name_length": 70}
{"curie": "MONDO:0043077", "names": ["weinstein kliman scully syndrome", "Weinstein Kliman Scully syndrome", "cardiomyopathy, hypogonadism and metabolic anomalies", "Cardiomyopathy, hypogonadism and metabolic anomalies", "primary testicular insufficiency with normal virilization, blindness, deafness and metabolic abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "weinstein kliman scully syndrome", "shortest_name_length": 32}
{"curie": "MONDO:0024609", "names": ["Epithelioma of vulva", "Vulva Epidermoid Carcinoma", "vulva epidermoid carcinoma", "VULVAR CANCER SQUAMOUS CELL", "Vulvar Epidermoid carcinoma", "Vulvar Squamous Cell Cancer", "vulvar squamous cell cancer", "Vulvar Epidermoid Carcinoma", "vulvar epidermoid carcinoma", "Epidermoid Carcinoma of Vulva", "epidermoid carcinoma of vulva", "carcinoma cell squamous vulva", "vulva squamous cell carcinoma", "squamous cell carcinoma vulva", "Vulva Squamous Cell Carcinoma", "Vulval squamous cell carcinoma", "vulvar squamous cell carcinoma", "Vulvar Squamous Cell Carcinoma", "Vulvar squamous cell carcinoma", "Vulva Epidermoid Cell Carcinoma", "vulva epidermoid cell carcinoma", "Squamous cell carcinoma of vulva", "Squamous Cell Carcinoma of Vulva", "Vulvar Epidermoid Cell Carcinoma", "squamous cell carcinoma of vulva", "vulvar epidermoid cell carcinoma", "Epidermoid Carcinoma of the Vulva", "epidermoid carcinoma of the vulva", "epidermoid cell carcinoma of vulva", "Epidermoid Cell Carcinoma of Vulva", "squamous cell carcinoma of the vulva", "Squamous cell carcinoma of the vulva", "Squamous Cell Carcinoma of the Vulva", "vulva, squamous cell carcinoma of the", "CA - Squamous cell carcinoma of vulva", "epidermoid cell carcinoma of the vulva", "Epidermoid Cell Carcinoma of the Vulva", "SCC - Squamous cell carcinoma of vulva", "mammalian vulva squamous cell carcinoma", "Squamous cell carcinoma of vulva (disorder)", "squamous cell carcinoma of vulva (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar squamous cell carcinoma", "shortest_name_length": 20}
{"curie": "UMLS:C4526904", "names": ["Stage III Soft Tissue Sarcoma of the Trunk and Extremities", "Stage III Soft Tissue Sarcoma of the Trunk and Extremities AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Soft Tissue Sarcoma of the Trunk and Extremities AJCC v8", "shortest_name_length": 58}
{"curie": "UMLS:C0220643", "names": ["Malignant Sinonasal Neoplasm", "Paranasal sinus and nasal cavity malignant neoplasm", "Malignant Nasal Cavity and Paranasal Sinus Neoplasm", "Paranasal sinus and nasal cavity malignant neoplasm NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paranasal sinus and nasal cavity malignant neoplasm", "shortest_name_length": 28}
{"curie": "UMLS:C5669923", "names": ["Infant-Type Hemispheric Glioma, MET-Altered"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infant-Type Hemispheric Glioma, MET-Altered", "shortest_name_length": 43}
{"curie": "UMLS:C4330043", "names": ["Gingival SCC", "Gingival Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gingival Squamous Cell Carcinoma", "shortest_name_length": 12}
{"curie": "OMIM:300306", "names": ["BMIQ11", "OBESITY, SUSCEPTIBILITY TO", "BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 6}
{"curie": "MONDO:0006322", "names": ["non-neoplastic bile duct disorder", "Non-Neoplastic Bile Duct Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-neoplastic bile duct disorder", "shortest_name_length": 33}
{"curie": "MONDO:0004707", "names": ["AIN3", "VIN III", "AIN III", "VIN, III", "vain iii", "VAIN III", "VAIN, III", "VAIN 3 AJCC v6", "VAIN III AJCC v6", "stage 0 anus cancer", "Anal cancer stage 0", "stage 0 anal cancer", "VAIN Grade 3 AJCC v6", "anal cancer, stage 0", "anus cancer, stage 0", "stage 0 vagina cancer", "VAGINAL CANCER IN SITU", "Anal carcinoma in situ", "Vaginal cancer in situ", "vagina cancer, stage 0", "anal carcinoma in situ", "Vaginal cancer stage 0", "stage 0 vaginal cancer", "Stage 0 Vaginal Cancer", "anal carcinoma stage 0", "vaginal cancer, stage 0", "Cancer of vagina stage 0", "vagina carcinoma in situ", "dysplasia; vulva, severe", "Cancer in situ of vagina", "severe dysplasia of vulva", "Stage 0 Anal Canal Cancer", "carcinoma in situ of anus", "Carcinoma in situ of anus", "Carcinoma in situ, vagina", "Severe dysplasia of vulva", "stage 0 anal canal cancer", "carcinoma in situ of vagina", "Carcinoma in situ of vagina", "Anal Canal Carcinoma in situ", "stage 0 anal canal carcinoma", "stage 0 cancer of the vagina", "anal canal carcinoma in situ", "anal canal in situ carcinoma", "Cancer in situ of anal canal", "cancer of the vagina, stage 0", "FIGO Stage 0 Vagina Carcinoma", "Vaginal Cancer Stage 0 AJCC v6", "stage 0 anal carcinoma in situ", "Stage 0 Vaginal Cancer AJCC v6", "AJCC Stage 0 Vaginal Cancer v6", "FIGO Stage 0 Vaginal Carcinoma", "Carcinoma in situ of anal canal", "carcinoma in situ of anal canal", "stage 0 carcinoma of the vagina", "Anal Intraepithelial Neoplasia 3", "FIGO Stage 0 Carcinoma of Vagina", "Carcinoma in situ of vagina, NOS", "carcinoma of the vagina, stage 0", "Vagina Carcinoma in situ AJCC v6", "stage 0 anal canal cancer aJCC v6", "Vaginal Carcinoma in situ AJCC v6", "Carcinoma in situ of skin of anus", "Stage 0 Anal Canal Cancer AJCC v7", "carcinoma in situ of skin of anus", "Stage 0 Anal Canal Cancer AJCC v6", "stage 0 anal canal cancer aJCC v7", "Carcinoma in situ of Vagina AJCC v6", "Carcinoma in situ of anus (disorder)", "FIGO Stage 0 Carcinoma of the Vagina", "Vulvar intraepithelial neoplasia III", "Vaginal intraepithelial neoplasia III", "Stage 0 Anal Carcinoma AJCC v6 and v7", "carcinoma in situ of anus (diagnosis)", "severe dysplasia of vulva (diagnosis)", "VAGINAL INTRAEPITHELIAL NEOPLASIA III", "stage 0 anal carcinoma aJCC v6 and v7", "Carcinoma in situ of anus, unspecified", "Carcinoma in situ of vagina (disorder)", "Carcinoma in situ of the Vagina AJCC v6", "carcinoma in situ of vagina (diagnosis)", "Anal intraepithelial neoplasia grade III", "Stage 0 Anal Canal Cancer AJCC v6 and v7", "anal intraepithelial neoplasia grade III", "stage 0 anal canal cancer aJCC v6 and v7", "Vulval intraepithelial neoplasia grade 3", "Anal Squamous Intraepithelial Neoplasia 3", "Vaginal intraepithelial neoplasia grade 3", "Anal intraepithelial neoplasia, grade III", "Carcinoma in situ of anal canal (disorder)", "vulvar intraepithelial neoplasia grade III", "VAIN - Vaginal intraepithelial neoplasia 3", "Vulval intraepithelial neoplasia grade III", "carcinoma in situ of anal canal (diagnosis)", "stage 0 anal canal carcinoma aJCC v6 and v7", "Stage 0 Anal Canal Carcinoma AJCC v6 and v7", "Vaginal intraepithelial neoplasia grade III", "vulva; intraepithelial neoplasia, grade III", "Vulvar intraepithelial neoplasia, grade III", "grade III intraepithelial neoplasia of vulva", "vagina; intraepithelial neoplasia, grade III", "neoplasia; intraepithelial, vulva, grade III", "Vaginal intraepithelial neoplasia, grade III", "neoplasia; intraepithelial, vagina, grade III", "carcinoma in situ of skin of anus (diagnosis)", "VIN - Vulval intraepithelial neoplasia grade 3", "Vaginal intraepithelial neoplasia III [VAIN III]", "Vaginal Intraepithelial Neoplasia Grade 3 AJCC v6", "Grade 3 Vaginal Intraepithelial Neoplasia AJCC v6", "Vulval high grade squamous intraepithelial lesion", "Intraepithelial Neoplasia of Vagina Grade 3 AJCC v6", "Grade III Vaginal Intraepithelial Neoplasia AJCC v6", "Vulval intraepithelial neoplasia grade 3 (disorder)", "VIN III - Vulval intraepithelial neoplasia grade III", "grade III squamous intraepithelial neoplasia of vagina", "VAIN III - Vaginal intraepithelial neoplasia grade III", "Intraepithelial Neoplasia of the Vagina Grade 3 AJCC v6", "Vulval HSIL (high grade squamous intraepithelial lesion)", "grade III intraepithelial neoplasia of vulva (diagnosis)", "grade III squamous intraepithelial neoplasia of vagina (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anal canal carcinoma in situ", "shortest_name_length": 4}
{"curie": "UMLS:C1334026", "names": ["HR GIST", "High Risk GIST", "High Risk Gastrointestinal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Risk Gastrointestinal Stromal Tumor", "shortest_name_length": 7}
{"curie": "MONDO:0018349", "names": ["MAN1B1-CDG", "MAN1B1-congenital disorder of glycosylation", "Intellectual disability-truncal obesity syndrome", "intellectual disability-truncal obesity syndrome", "Congenital disorder of glycosylation type 2 due to MAN1B1 deficiency", "congenital disorder of glycosylation type 2 due to MAN1B1 deficiency", "congenital disorder of glycosylation type II due to MAN1B1 deficiency", "Congenital disorder of glycosylation type II due to MAN1B1 deficiency", "Carbohydrate deficient glycoprotein syndrome type II due to MAN1B1 deficiency", "carbohydrate deficient glycoprotein syndrome type II due to MAN1B1 deficiency", "MAN1B1-CDG - mannosidase alpha class 1B member 1 deficiency congenital disorder of glycosylation", "Carbohydrate deficient glycoprotein syndrome type 2 due to deficiency of mannosidase alpha class 1B member 1", "Carbohydrate deficient glycoprotein syndrome type 2 due to deficiency of mannosidase alpha class 1B member 1 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MAN1B1-congenital disorder of glycosylation", "shortest_name_length": 10}
{"curie": "UMLS:C0585136", "names": ["RETENION GASTRIC", "Gastric retention", "gastric retention", "Retention gastric", "Gastric retention (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric retention", "shortest_name_length": 16}
{"curie": "MONDO:0017386", "names": ["anaplastic rhabdomyosarcoma", "anaplastic Rhabdomyosarcoma", "Pleomorphic rhabdomyosarcoma", "pleomorphic rhabdomyosarcoma", "Pleomorphic Rhabdomyosarcoma", "rhabdomyosarcoma pleomorphic", "pleomorphic; rhabdomyosarcoma", "rhabdomyosarcoma; pleomorphic", "Pleomorphic rhabdomyosarcoma, NOS", "Pleomorphic rhabdomyosarcoma (disorder)", "pleomorphic rhabdomyosarcoma, adult type", "Pleomorphic rhabdomyosarcoma, adult type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pleomorphic rhabdomyosarcoma", "shortest_name_length": 27}
{"curie": "MONDO:0000256", "names": ["Systemic mycosis", "mycosis systemic", "systemic mycosis", "Disseminated mycosis", "Systemic mycosis, NOS", "fungal infection systemic", "Systemic fungal infection", "systemic fungal infection", "fungal infections systemic", "Systemic mycosis (disorder)", "Systemic mycosis (diagnosis)", "Systemic fungal infection NOS", "Systemic fungal infection, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "systemic mycosis", "shortest_name_length": 16}
{"curie": "UMLS:C0854176", "names": ["Malignant Hepatobiliary Neoplasm", "Malignant hepatobiliary neoplasm", "Malignant hepatobiliary neoplasms", "Malignant Hepato-Biliary Neoplasm", "Malignant hepatobiliary neoplasm NOS", "Malignant Liver and Biliary Neoplasm", "Malignant Liver and Biliary System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant hepatobiliary neoplasms", "shortest_name_length": 32}
{"curie": "UMLS:C0236818", "names": ["elective mutism", "Elective mutism", "Elective Mutism", "Voluntary Mutism", "Selective mutism", "mutism selective", "Selective Mutism", "selective mutism", "mutism; elective", "Mutism, Elective", "elective; mutism", "refusal to speak", "Elective Mutisms", "voluntary mutism", "Mutisms, Elective", "selective; mutism", "Voluntary Mutisms", "Mutism, Voluntary", "Mutism, Selective", "mutism; selective", "Mutisms, Voluntary", "refusal to speak (symptom)", "Elective mutism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Selective Mutism", "shortest_name_length": 15}
{"curie": "MONDO:0011546", "names": ["Htx", "HTX", "HTX2", "DTGA2", "heterotaxy, visceral, 2, autosomal", "HETEROTAXY, VISCERAL, 2, AUTOSOMAL", "transposition of the great arteries, dextro-looped 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heterotaxy, visceral, 2, autosomal", "shortest_name_length": 3}
{"curie": "MONDO:0015070", "names": ["larynx NET", "Laryngeal endocrine tumor", "Laryngeal endocrine tumour", "larynx neuroendocrine tumor", "neuroendocrine tumor of larynx", "laryngeal neuroendocrine tumor", "neuroendocrine tumor of Larynx", "Larynx Neuroendocrine Neoplasm", "larynx neuroendocrine neoplasm", "neuroendocrine tumour of Larynx", "laryngeal neuroendocrine tumour", "neuroendocrine neoplasm of larynx", "laryngeal neuroendocrine neoplasm", "Neuroendocrine Neoplasm of Larynx", "Laryngeal Neuroendocrine Neoplasm", "Neuroendocrine neoplasm of larynx", "neuroendocrine neoplasm of the larynx", "Neuroendocrine Neoplasm of the Larynx", "Neuroendocrine neoplasm of larynx (disorder)", "larynx neuroendocrine tumor, well differentiated, low or intermediate grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laryngeal neuroendocrine neoplasm", "shortest_name_length": 10}
{"curie": "MONDO:0002795", "names": ["Adult CNS PNET", "adult CNS PNET", "Adult CNS Primitive Neuroectodermal Tumor", "adult CNS primitive neuroectodermal tumor", "adult CNS primitive neuroectodermal neoplasm", "Adult CNS Primitive Neuroectodermal Neoplasm", "adult central nervous system embryonal tumor", "Adult Central Primitive Neuroectodermal Tumour", "adult central primitive neuroectodermal tumour", "Adult Central Primitive Neuroectodermal Neoplasm", "adult central primitive neuroectodermal neoplasm", "Adult Central Nervous System Embryonal Tumor, NOS", "adult central nervous system primitive neuroectodermal tumor", "Adult Central Nervous System Primitive Neuroectodermal Tumor", "adult central nervous system primitive neuroectodermal neoplasm", "Adult Central Nervous System Primitive Neuroectodermal Neoplasm", "central nervous system primitive neuroectodermal neoplasm of adults", "Adult Central Nervous System Embryonal Tumor, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult central nervous system primitive neuroectodermal neoplasm", "shortest_name_length": 14}
{"curie": "MONDO:0013557", "names": ["HPS5", "HERMANSKY-PUDLAK SYNDROME 5", "Hermansky-Pudlak syndrome 5", "HPS5 Hermansky-Pudlak syndrome", "Hermansky-Pudlak syndrome type 5", "Hermansky-Pudlak syndrome caused by mutation in HPS5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hermansky-Pudlak syndrome 5", "shortest_name_length": 4}
{"curie": "UMLS:C1336394", "names": ["Stage IVC Laryngeal Cancer", "Stage IVC Larynx Carcinoma", "stage IVC laryngeal cancer", "Laryngeal Cancer Stage IVC", "Stage IVC Laryngeal Carcinoma", "Stage IVC Carcinoma of Larynx", "Stage IVC Laryngeal Throat Cancer", "Stage IVC Carcinoma of the Larynx", "Stage IVC Laryngeal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Laryngeal Cancer AJCC v7", "shortest_name_length": 26}
{"curie": "MONDO:0017847", "names": ["AR-SPAX", "autosomal recessive spastic ataxia", "spastic ataxia, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive spastic ataxia", "shortest_name_length": 7}
{"curie": "MONDO:0021098", "names": ["Papillomatosis", "papillomatosis", "papillomatoses", "Papillomatoses", "Papillomatosis NOS", "Papillomatosis, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papillomatosis", "shortest_name_length": 14}
{"curie": "UMLS:C0278839", "names": ["Recurrent Skin Cancer", "recurrent skin cancer", "skin cancer, recurrent", "Recurrent Skin Carcinoma", "Recurrent Cancer of Skin", "Recurrent Carcinoma of Skin", "Recurrent Cancer of the Skin", "recurrent cancer of the skin", "cancer of the skin, recurrent", "Recurrent Cutaneous Carcinoma", "recurrent carcinoma of the skin", "Recurrent Carcinoma of the Skin", "carcinoma of the skin, recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Skin Carcinoma", "shortest_name_length": 21}
{"curie": "UMLS:C5446867", "names": ["Unresectable Abdominal Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Abdominal Neuroendocrine Neoplasm", "shortest_name_length": 46}
{"curie": "UMLS:C0340908", "names": ["AV Fistula Stenosis", "Arteriovenous Fistula Stenosis", "Arteriovenous fistula stenosis", "Arteriovenous fistula stenosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arteriovenous fistula stenosis", "shortest_name_length": 19}
{"curie": "MONDO:0017180", "names": ["dup(10)(q22.3q23.3)", "trisomy 10q22.3q23.3", "10q22.3q23.3 microduplication syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "10q22.3q23.3 microduplication syndrome", "shortest_name_length": 19}
{"curie": "MONDO:0017782", "names": ["developmental and speech delay due to SOX5 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and speech delay due to SOX5 deficiency", "shortest_name_length": 53}
{"curie": "UMLS:C0281642", "names": ["Pediatric Acute M0 Leukemia", "childhood acute M0 leukemia", "pediatric acute M0 leukemia", "Childhood Acute M0 Leukemia", "M0 leukemia, pediatric acute", "M0 leukemia, childhood acute", "Childhood Acute Minimally Differentiated Myeloid Leukemia", "Pediatric Acute Minimally Differentiated Myeloid Leukemia", "Childhood Acute Myeloid Leukemia Minimally Differentiated", "Acute Myeloid Leukemia (AML) with Minimal Differentiation", "M0 pediatric acute minimally differentiated myeloid leukemia", "M0 childhood acute minimally differentiated myeloid leukemia", "M0 Childhood Acute Minimally Differentiated Myeloid Leukemia", "M0 Pediatric Acute Minimally Differentiated Myeloid Leukemia", "Childhood Acute Myeloid Leukemia with Minimal Differentiation", "pediatric acute minimally differentiated myeloid leukemia (M0)", "Childhood Acute Minimally Differentiated Myeloid Leukemia (M0)", "childhood acute minimally differentiated myeloid leukemia (M0)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Acute Myeloid Leukemia with Minimal Differentiation", "shortest_name_length": 27}
{"curie": "MONDO:0003288", "names": ["bizarre leiomyoma", "Bizarre leiomyoma", "Bizarre Leiomyoma", "Atypical Leiomyoma", "atypical leiomyoma", "Atypical leiomyoma", "Symplastic leiomyoma", "symplastic leiomyoma", "pleomorphic leiomyoma", "Pleomorphic Leiomyoma", "Pleomorphic leiomyoma", "Bizarre leiomyoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bizarre leiomyoma", "shortest_name_length": 17}
{"curie": "MONDO:0003333", "names": ["Benign Struma Ovarii", "benign struma ovarii", "struma ovarii, benign"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign struma ovarii", "shortest_name_length": 20}
{"curie": "UMLS:C0920184", "names": ["Fundic gland polyp", "Fundic Gland Polyp", "fundic gland polyp", "fundic gland polyps", "Polyps, fundic gland", "Fundic gland polyp (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fundic gland polyp", "shortest_name_length": 18}
{"curie": "MONDO:0009014", "names": ["CNA2", "Cornea Plana 2", "cornea plana 2", "CORNEA PLANA 2", "KERA cornea plana", "cornea plana type 2", "CORNEA PLANA 2, AUTOSOMAL RECESSIVE", "cornea plana 2, autosomal recessive", "cornea plana caused by mutation in KERA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cornea plana 2", "shortest_name_length": 4}
{"curie": "UMLS:C3900091", "names": ["Unfavorable Prognosis Hodgkin Lymphoma", "Adult Unfavorable Prognosis Hodgkin Lymphoma", "adult unfavorable prognosis Hodgkin lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Unfavorable Prognosis Hodgkin Lymphoma", "shortest_name_length": 38}
{"curie": "UMLS:C4054391", "names": ["Nephrotic Syndrome - CUBN Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - CUBN Associated", "shortest_name_length": 36}
{"curie": "MONDO:0019437", "names": ["era", "ERA", "Juvenile ERA", "Enthesitis-Related JIA", "enthesitis-related JIA", "Enthesitis-related JIA", "juvenile spondylarthropathy", "Enthesitis related arthritis", "Enthesitis-Related Arthritis", "enthesitis-related arthritis", "juvenile enthesitis-related arthritis", "enthesitis related arthritis, juvenile", "Enthesitis-Related Juvenile Idiopathic Arthritis", "Enthesitis-related juvenile idiopathic arthritis", "enthesitis-related juvenile idiopathic arthritis", "Juvenile idiopathic arthritis, enthesitis related arthritis", "Juvenile idiopathic arthritis, enthesitis related arthritis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "enthesitis-related juvenile idiopathic arthritis", "shortest_name_length": 3}
{"curie": "UMLS:C4015932", "names": ["Carbonic Anhydrase I Deficiency", "CARBONIC ANHYDRASE I DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CARBONIC ANHYDRASE I DEFICIENCY", "shortest_name_length": 31}
{"curie": "MONDO:0018714", "names": ["pila", "PILA", "dabska tumor", "Dabska Tumor", "Dabska tumor", "Dabska tumour", "Endovascular papillary angioendothelioma", "Papillary Endovascular Angioendothelioma", "primary intralymphatic angioendothelioma", "papillary Endovascular angioendothelioma", "Primary intralymphatic angioendothelioma", "papillary intralymphatic angioendothelioma", "Papillary intralymphatic angioendothelioma", "Papillary Intralymphatic Angioendothelioma", "Papillary intralymphatic angioendomethelioma", "malignant endothelial papillary angioendothelioma", "Malignant Endothelial Papillary Angioendothelioma", "Papillary intralymphatic angioendothelioma (disorder)", "Papillary intralymphatic angioendothelioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary intralymphatic angioendothelioma", "shortest_name_length": 4}
{"curie": "UMLS:C0268769", "names": ["NEPHROPATHY GOUTY", "Gouty Nephropathy", "Gouty nephropathy", "gouty nephropathy", "Gouty renal disease", "GOUT, RENAL DISEASE", "Gouty kidney disease", "Chronic gouty nephropathy", "GOUTY NEPHROPATHY CHRONIC", "Chronic urate nephropathy", "Chronic Urate Nephropathy", "gouty nephropathy (diagnosis)", "Gouty nephropathy, unspecified", "Chronic urate nephropathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic gouty nephropathy", "shortest_name_length": 17}
{"curie": "MONDO:0015606", "names": ["Del(X)(p23)", "Xp22.3 microdeletion syndrome", "Chromosome Xp22.3 microdeletion syndrome", "Chromosome Xp22.3 microdeletion syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Xp22.3 microdeletion syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0030634", "names": ["HDLS2", "LEUKOENCEPHALOPATHY, HEREDITARY DIFFUSE, WITH SPHEROIDS 2", "leukoencephalopathy, hereditary diffuse, with spheroids 2", "leukoencephalopathy, hereditary diffuse, with spheroids, swedish IIA", "LEUKOENCEPHALOPATHY, HEREDITARY DIFFUSE, WITH SPHEROIDS, SWEDISH TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukoencephalopathy, hereditary diffuse, with spheroids 2", "shortest_name_length": 5}
{"curie": "MONDO:0003635", "names": ["sebaceous breast carcinoma", "Breast Sebaceous Carcinoma", "breast sebaceous adenocarcinoma", "sebaceous adenocarcinoma of breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sebaceous breast carcinoma", "shortest_name_length": 26}
{"curie": "UMLS:C4526724", "names": ["Stage IIIC Lung Cancer", "Stage IIIC Lung Cancer AJCC v8", "stage IIIC lung cancer AJCC v8", "stage IIIC non-small cell lung cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Lung Cancer AJCC v8", "shortest_name_length": 22}
{"curie": "MONDO:0016391", "names": ["NDM", "neonatal diabetes", "Neonatal diabetes", "neonatal; diabetes", "diabetes; neonatal", "neonatal diabetes mellitus", "Neonatal diabetes mellitus", "Neonatal Diabetes Mellitus", "congenital diabetes mellitus", "Congenital Diabetes Mellitus", "Neonatal diabetes mellitus (disorder)", "neonatal diabetes mellitus (diagnosis)", "diabetes mellitus syndrome in newborn infant", "Diabetes mellitus syndrome in newborn infant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal diabetes mellitus", "shortest_name_length": 3}
{"curie": "UMLS:C1511269", "names": ["Borderline Ovarian Serous Surface Papillary Tumor", "Borderline Ovarian Serous Surface Papillary Neoplasm", "Serous surface papillary tumor of borderline malignancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Ovarian Serous Surface Papillary Tumor", "shortest_name_length": 49}
{"curie": "MONDO:0017066", "names": ["Cervical spina bifida aperta", "cervical spina bifida aperta", "Spina bifida aperta of cervical spine", "Spina bifida aperta of cervical spine (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical spina bifida aperta", "shortest_name_length": 28}
{"curie": "UMLS:C0694575", "names": ["macular fibrosis", "fibrosis macular", "Macular fibrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Macular fibrosis", "shortest_name_length": 16}
{"curie": "MONDO:0009506", "names": ["SGD", "Specific Granule Deficiency", "specific granule deficiency", "Specific granule deficiency", "NEUTROPHIL LACTOFERRIN DEFICIENCY", "SGD - Specific granule deficiency", "Lactoferrin-Deficient Neutrophils", "LACTOFERRIN-DEFICIENT NEUTROPHILS", "Neutrophil lactoferrin deficiency", "Neutrophil Lactoferrin Deficiency", "lactoferrin-deficient neutrophils", "neutrophil lactoferrin deficiency", "Specific granule deficiency (disorder)", "neutrophil-specific granule deficiency", "Neutrophil lactoferrin deficiency (disorder)", "neutrophil lactoferrin deficiency (diagnosis)", "recurrent infection due to specific granule deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "specific granule deficiency", "shortest_name_length": 3}
{"curie": "UMLS:C5417751", "names": ["CCS/ GNET", "Gastrointestinal Clear Cell Sarcoma/Malignant Gastrointestinal Neuroectodermal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal Clear Cell Sarcoma/Malignant Gastrointestinal Neuroectodermal Tumor", "shortest_name_length": 9}
{"curie": "MONDO:0024392", "names": ["Anaerobic balanitis", "anaerobic balanitis", "Anaerobic balanitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anaerobic balanitis", "shortest_name_length": 19}
{"curie": "MONDO:0016296", "names": ["HPE", "HPEC", "HPE, FAMILIAL", "Holoprosencephaly", "holoprosencephaly", "Holoprosencephalies", "Single brain ventricle", "Holoprosencephaly (HPE)", "HPE - Holoprosencephaly", "Holoprosencephaly Sequence", "holoprosencephaly sequence", "Holoprosencephaly sequence", "holoprosencephaly (diagnosis)", "Familial alobar holoprosencephaly", "Holoprosencephaly sequence (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "holoprosencephaly", "shortest_name_length": 3}
{"curie": "MONDO:0013209", "names": ["NAFL", "NAFLD", "NAFLD1", "Nonalcoholic Fatty Liver", "nonalcoholic fatty liver", "Nonalcoholic fatty liver", "non-alcoholic fatty liver", "Fatty Liver, Nonalcoholic", "Nonalcoholic Fatty Livers", "Non-alcoholic fatty liver", "Liver, Nonalcoholic Fatty", "Livers, Nonalcoholic Fatty", "Fatty Livers, Nonalcoholic", "nonalcoholic fatty liver disease", "Nonalcoholic fatty liver disease", "NAFL - non-alcoholic fatty liver", "Nonalcoholic Fatty Liver Disease", "Non-alcoholic Fatty Liver Disease", "non-alcoholic fatty liver disease", "Non-Alcoholic Fatty Liver Disease", "Non-alcoholic fatty liver disease", "fatty liver disease, nonalcoholic", "Non alcoholic Fatty Liver Disease", "nonalcoholic fatty liver (diagnosis)", "Non-alcoholic fatty liver (disorder)", "NAFLD - Nonalcoholic Fatty Liver Disease", "Nonalcoholic fatty liver disease (NAFLD)", "NAFLD - nonalcoholic fatty liver disease", "Non-alcoholic fatty liver disease (disorder)", "liver disease, alcoholic, susceptibility to, 1", "fatty liver disease, nonalcoholic, susceptibility to, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-alcoholic fatty liver disease", "shortest_name_length": 4}
{"curie": "UMLS:C1520098", "names": ["Vulvar Superficial Angiomyxoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Superficial Angiomyxoma", "shortest_name_length": 30}
{"curie": "UMLS:C0423711", "names": ["Perineal Neuralgia", "Perineal neuralgia", "Neuralgia, Perineal", "Perineal Neuralgias", "Neuralgias, Perineal", "Perineal neuralgia (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neuralgia, Perineal", "shortest_name_length": 18}
{"curie": "MONDO:0020160", "names": ["secondary entropion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary entropion", "shortest_name_length": 19}
{"curie": "UMLS:C0279943", "names": ["pediatric STS, recurrent", "childhood STS, recurrent", "STS, childhood, recurrent", "STS, recurrent, childhood", "Recurrent Soft Tissue Sarcoma", "Relapsed Pediatric Soft Tissue Sarcoma", "Relapsed Childhood Soft Tissue Sarcoma", "recurrent childhood soft tissue sarcoma", "Recurrent Pediatric Soft Tissue Sarcoma", "Recurrent Childhood Soft Tissue Sarcoma", "pediatric soft tissue sarcoma, recurrent", "childhood soft tissue sarcoma, recurrent", "Relapsed Childhood Sarcoma of Soft Tissue", "Relapsed Pediatric Sarcoma of Soft Tissue", "Recurrent Childhood Sarcoma of Soft Tissue", "Recurrent Pediatric Sarcoma of Soft Tissue", "Relapsed Childhood Sarcoma of the Soft Tissue", "Relapsed Pediatric Sarcoma of the Soft Tissue", "Recurrent Childhood Sarcoma of the Soft Tissue", "Recurrent Pediatric Sarcoma of the Soft Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Soft Tissue Sarcoma", "shortest_name_length": 24}
{"curie": "UMLS:C2347926", "names": ["Refractory Spinal Cord Tumor", "Refractory Spinal Cord Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Spinal Cord Neoplasm", "shortest_name_length": 28}
{"curie": "UMLS:C0751718", "names": ["Late Infantile Neuroaxonal Dystrophy", "Neuroaxonal Dystrophy, Late Infantile"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Late Infantile Neuroaxonal Dystrophy", "shortest_name_length": 36}
{"curie": "MONDO:0015445", "names": ["autosomal dominant aorta coarctation", "aorta coarctation, autosomal dominant", "autosomal dominant coarctation of aorta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant coarctation of aorta", "shortest_name_length": 36}
{"curie": "UMLS:C2981384", "names": ["Stage I Appendix Cancer", "Stage I Appendix Carcinoma", "Stage I Appendix Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Appendix Carcinoma AJCC v7", "shortest_name_length": 23}
{"curie": "MONDO:0001752", "names": ["Alveoalgia", "Dry Socket", "Dry socket", "dry socket", "dry sockets", "Socket, Dry", "Dry Sockets", "Alveolalgia", "dry; socket", "socket; dry", "Alveolalgias", "Sockets, Dry", "Dry socket NOS", "jaw; alveolitis", "alveolitis; jaw", "dry tooth socket", "tooth dry socket", "dry socket tooth", "Dry tooth socket", "alveolitis of jaw", "alveolar osteitis", "Alveolar Osteitis", "Alveolar osteitis", "Alveolitis of jaw", "alveolar; osteitis", "Alveolitis of jaws", "Osteitis, Alveolar", "osteitis; alveolar", "Alveolar Osteitides", "Osteitides, Alveolar", "periostitis alveolar", "Alveolar Periostitis", "Alveolar periostitis", "alveolar periostitis", "periostitis; alveolar", "alveolar; periostitis", "Periostitis, Alveolar", "Alveolitis of jaw, NOS", "Alveolar Periostitides", "Periostitides, Alveolar", "Alveolitis sicca dolorosa", "Alveolitis Sicca Dolorosa", "alveolitis sicca dolorosa", "Alveolitis of jaw (disorder)", "dry socket alveolitis of jaw", "alveolitis of jaw (diagnosis)", "Alveolar periostitis (disorder)", "Alveolar periostitis (diagnosis)", "dry socket alveolitis of jaw (diagnosis)", "jaw skeleton extrinsic allergic alveolitis", "extrinsic allergic alveolitis of jaw skeleton"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alveolar periostitis", "shortest_name_length": 10}
{"curie": "MONDO:0001861", "names": ["malignant parietal pleura tumor", "primary malignant neoplasm of parietal pleura", "Primary malignant neoplasm of parietal pleura", "lung neoplasm malignant parietal pleura primary", "Primary malignant neoplasm of parietal pleura (disorder)", "Primary malignant neoplasm of parietal pleura (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant parietal pleura tumor", "shortest_name_length": 31}
{"curie": "UMLS:C2350344", "names": ["Chronic Lung Injury", "Lung Injury, Chronic", "Chronic Lung Injuries", "Lung Injuries, Chronic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic Lung Injury", "shortest_name_length": 19}
{"curie": "MONDO:0022769", "names": ["ciliary dyskinesia-bronchiectasis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ciliary dyskinesia-bronchiectasis", "shortest_name_length": 33}
{"curie": "UMLS:C2347749", "names": ["Grade III Meningioma", "Adult Grade 3 Meningioma", "Adult Grade III Meningioma", "adult grade III meningioma", "grade III meningioma, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Grade III Meningioma", "shortest_name_length": 20}
{"curie": "UMLS:C1710629", "names": ["Ventricular myxoma", "Ventricular Myxoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ventricular myxoma", "shortest_name_length": 18}
{"curie": "UMLS:C4726593", "names": ["Refractory Burkitt Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Burkitt Leukemia", "shortest_name_length": 27}
{"curie": "UMLS:C5420808", "names": ["Conjunctival Spitz Nevus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conjunctival Spitz Nevus", "shortest_name_length": 24}
{"curie": "MONDO:0044739", "names": ["SJS/TEN overlap syndrome", "Stevens-Johnson/TEN overlap syndrome", "Stevens-Johnson/toxic epidermal necrolysis overlap syndrome", "Stevens-Johnson syndrome/toxic epidermal necrolysis overlap syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stevens-Johnson syndrome/toxic epidermal necrolysis overlap syndrome", "shortest_name_length": 24}
{"curie": "MONDO:0016955", "names": ["Trisomy 4q", "4q trisomy", "trisomy 4q", "4q syndrome", "4q+ syndrome", "4q duplication", "Duplication 4q", "dup(4q) syndrome", "Distal 4q Trisomy", "distal 4q trisomy", "partial trisomy 4q", "chromosome 4q trisomy", "duplication 4q syndrome", "4q duplication syndrome", "Chromosome 4, trisomy 4q", "Dup(4q) Syndrome, Partial", "partial trisomy distal 4q", "dup(4q) syndrome, partial", "chromosome 4q duplication", "Partial Trisomy 4q Syndrome", "partial trisomy 4q syndrome", "Duplication 4q syndrome, partial", "Chromosome 4, Partial Trisomy 4q", "chromosome 4, partial trisomy 4q", "Duplication 4q Syndrome, Partial", "partial trisomy of chromosome 4q", "chromosome 4q duplication syndrome", "partial duplication of chromosome 4q", "partial trisomy of the long arm of chromosome 4", "partial duplication of the long arm of chromosome 4", "partial duplication of the long arm of chromosome type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of the long arm of chromosome 4", "shortest_name_length": 10}
{"curie": "UMLS:C1299683", "names": ["Zonular dehiscence", "Zonular Dehiscence", "Zonular dehiscence (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Zonular dehiscence", "shortest_name_length": 18}
{"curie": "MONDO:0003271", "names": ["hypothyroidism iodine", "Iodine hypothyroidism", "iodine hypothyroidism", "hypothyroidism acquired iodine", "Iodine hypothyroidism (disorder)", "Iodine hypothyroidism (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "iodine hypothyroidism", "shortest_name_length": 21}
{"curie": "MONDO:0009332", "names": ["Congenital hematological disorder", "congenital hematological disorder", "Congenital Hematological Disorder", "Congenital haematological disorder", "congenital hematological system disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital hematological disorder", "shortest_name_length": 33}
{"curie": "MONDO:0006038", "names": ["Indeterminate colitis", "indeterminate colitis", "colitis of indeterminate type", "Colitis of Indeterminate Type", "Indeterminate colitis (disorder)", "indeterminate colitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "indeterminate colitis", "shortest_name_length": 21}
{"curie": "MONDO:0010048", "names": ["Spastic Paraplegia With Myoclonic Epilepsy", "spastic paraplegia with myoclonic epilepsy", "SPASTIC PARAPLEGIA WITH MYOCLONIC EPILEPSY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic paraplegia with myoclonic epilepsy", "shortest_name_length": 42}
{"curie": "UMLS:C1565321", "names": ["Cholera Infantum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cholera Infantum", "shortest_name_length": 16}
{"curie": "UMLS:C0043046", "names": ["wasting disease", "Wasting Disease", "Wasting disease", "Wasting Syndrome", "wasting diseases", "Wasting syndrome", "Wasting Diseases", "wasting syndrome", "disease; wasting", "WASTING SYNDROME", "wasting; disease", "wasting; syndrome", "syndrome; wasting", "Wasting Syndromes", "WASTING GENERALIZED", "Wasting generalized", "Wasting generalised", "Wasting disease, NOS", "Wasting disease (disorder)", "disease (or disorder); wasting", "Malnutrition/starvation/cachexia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wasting Syndrome", "shortest_name_length": 15}
{"curie": "UMLS:C5204292", "names": ["Adenosquamous Carcinoma of the Penis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenosquamous Carcinoma of the Penis", "shortest_name_length": 36}
{"curie": "UMLS:C4288914", "names": ["Unidentified Immunodeficiency", "Immunodeficiency of Unknown Origin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immunodeficiency of Unknown Origin", "shortest_name_length": 29}
{"curie": "UMLS:C5668160", "names": ["Recurrent Small Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Small Cell Neuroendocrine Carcinoma", "shortest_name_length": 45}
{"curie": "MONDO:0000595", "names": ["sexual disorder", "sexual health disorder", "sexual and gender identity disorders", "Sexual and Gender Identity Disorders", "Sexual and gender identity disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sexual and gender identity disorders", "shortest_name_length": 15}
{"curie": "MONDO:0014635", "names": ["MCOPCB10", "MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 10", "microphthalmia, isolated, with coloboma 10", "RBP4 microphthalmia, isolated, with coloboma", "microphthalmia, isolated, with coloboma type 10", "microphthalmia, isolated, with coloboma caused by mutation in RBP4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microphthalmia, isolated, with coloboma 10", "shortest_name_length": 8}
{"curie": "UMLS:C1708786", "names": ["Lung Synovial Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Synovial Sarcoma", "shortest_name_length": 21}
{"curie": "UMLS:C0278802", "names": ["recurrent uterine cancer", "uterine cancer, recurrent", "Recurrent Endometrial Cancer", "Endometrial cancer recurrent", "recurrent endometrial cancer", "endometrial cancer, recurrent", "Endometrial carcinoma recurrent", "Recurrent Endometrial Carcinoma", "recurrent endometrial carcinoma", "Carcinoma endometrial recurrent", "Cancer of endometrium recurrent", "endometrial carcinoma, recurrent", "recurrent cancer of the endometrium", "cancer of the endometrium, recurrent", "recurrent carcinoma of the endometrium", "carcinoma of the endometrium, recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Endometrial Cancer", "shortest_name_length": 24}
{"curie": "UMLS:C1335967", "names": ["Simple without cytologic atypia", "Simple Endometrial Hyperplasia without Atypia", "Simple endometrial hyperplasia without atypia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Simple Endometrial Hyperplasia without Atypia", "shortest_name_length": 31}
{"curie": "MONDO:0009882", "names": ["Plasma Clot Retraction Factor, Deficiency of", "plasma clot retraction factor, deficiency of", "PLASMA CLOT RETRACTION FACTOR, DEFICIENCY OF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "plasma clot retraction factor, deficiency of", "shortest_name_length": 44}
{"curie": "MONDO:0006069", "names": ["Metastatic ACTH-Producing PitNET", "malignant pituitary Corticotropinoma", "Malignant Pituitary Corticotropinoma", "malignant Corticotropinoma of pituitary", "Malignant Corticotropinoma of Pituitary", "ACTH producing pituitary gland carcinoma", "ACTH-producing pituitary gland carcinoma", "malignant ACTH producing pituitary tumor", "ACTH Producing Pituitary Gland Carcinoma", "malignant ACTH secreting pituitary tumor", "Malignant ACTH Secreting Pituitary Tumor", "ACTH-Producing Pituitary Gland Carcinoma", "Malignant ACTH Producing Pituitary Tumor", "malignant pituitary gland Corticotropinoma", "Malignant Pituitary Gland Corticotropinoma", "Malignant ACTH Producing Tumor of Pituitary", "malignant ACTH producing tumor of pituitary", "malignant Corticotropinoma of the Pituitary", "Malignant ACTH Secreting Pituitary Neoplasm", "malignant ACTH secreting pituitary neoplasm", "Malignant ACTH Secreting Tumor of Pituitary", "malignant ACTH secreting tumor of pituitary", "malignant ACTH producing pituitary neoplasm", "Malignant ACTH Producing Pituitary Neoplasm", "Malignant Corticotropinoma of the Pituitary", "malignant Corticotropinoma of the pituitary", "malignant Corticotropinoma of pituitary gland", "Malignant Corticotropinoma of Pituitary Gland", "malignant ACTH secreting pituitary gland tumor", "Malignant ACTH Producing Pituitary Gland Tumor", "malignant ACTH producing pituitary gland tumor", "malignant ACTH secreting neoplasm of pituitary", "Malignant ACTH Secreting Pituitary Gland Tumor", "Malignant ACTH Producing Neoplasm of Pituitary", "Malignant ACTH Secreting Neoplasm of Pituitary", "malignant ACTH producing neoplasm of pituitary", "malignant ACTH secreting tumor of the pituitary", "Malignant ACTH Producing Tumor of the Pituitary", "malignant ACTH producing tumor of the pituitary", "Malignant ACTH Secreting Tumor of the Pituitary", "Malignant ACTH Secreting Tumor of Pituitary Gland", "malignant ACTH producing pituitary gland neoplasm", "malignant ACTH secreting tumor of pituitary gland", "Malignant ACTH Producing Tumor of Pituitary Gland", "malignant Corticotropinoma of the pituitary gland", "Malignant Corticotropinoma of the Pituitary Gland", "Malignant ACTH Producing Pituitary Gland Neoplasm", "malignant ACTH producing tumor of pituitary gland", "Malignant ACTH Secreting Neoplasm of the Pituitary", "malignant ACTH producing neoplasm of the pituitary", "Malignant ACTH Producing Neoplasm of the Pituitary", "malignant ACTH secreting neoplasm of the pituitary", "malignant ACTH secreting neoplasm of pituitary gland", "malignant ACTH producing neoplasm of pituitary gland", "Malignant ACTH Secreting Neoplasm of Pituitary Gland", "Malignant ACTH Producing Neoplasm of Pituitary Gland", "malignant ACTH secreting tumor of the pituitary gland", "Malignant ACTH Producing Tumor of the Pituitary Gland", "Malignant ACTH Secreting Tumor of the Pituitary Gland", "malignant ACTH producing tumor of the pituitary gland", "Metastatic Corticotroph Pituitary Neuroendocrine Tumor", "Malignant Adrenocorticotropin Producing Pituitary Tumor", "malignant adrenocorticotropin secreting pituitary tumor", "malignant adrenocorticotropin producing pituitary tumor", "Malignant Adrenocorticotropin Secreting Pituitary Tumor", "Malignant ACTH Secreting Neoplasm of the Pituitary Gland", "malignant ACTH producing neoplasm of the pituitary gland", "malignant ACTH secreting neoplasm of the pituitary gland", "Malignant ACTH Producing Neoplasm of the Pituitary Gland", "Malignant Adrenocorticotropin Producing Tumor of Pituitary", "Malignant Adrenocorticotropin Producing Pituitary Neoplasm", "malignant adrenocorticotropin producing tumor of pituitary", "Malignant Adrenocorticotropin Secreting Pituitary Neoplasm", "malignant adrenocorticotropin producing pituitary neoplasm", "malignant corticotropin secreting pituitary gland neoplasm", "malignant adrenocorticotropin secreting pituitary neoplasm", "Malignant Corticotropin Secreting Pituitary Gland Neoplasm", "malignant adrenocorticotropin producing pituitary gland tumor", "Malignant Adrenocorticotropin Secreting Pituitary Gland Tumor", "Malignant Adrenocorticotropin Producing Neoplasm of Pituitary", "Malignant Adrenocorticotropin Producing Pituitary Gland Tumor", "malignant adrenocorticotropin secreting pituitary gland tumor", "malignant adrenocorticotropin producing neoplasm of pituitary", "Malignant Adrenocorticotropin Producing Tumor of the Pituitary", "malignant adrenocorticotropin producing tumor of the pituitary", "Malignant Adrenocorticotropin Producing Tumor of Pituitary Gland", "Malignant Adrenocorticotropin Secreting Pituitary Gland Neoplasm", "malignant adrenocorticotropin producing pituitary gland neoplasm", "malignant adrenocorticotropin secreting pituitary gland neoplasm", "malignant adrenocorticotropin producing tumor of pituitary gland", "Malignant Adrenocorticotropin Producing Pituitary Gland Neoplasm", "Malignant Adrenocorticotropin Producing Neoplasm of the Pituitary", "malignant adrenocorticotropin producing neoplasm of the pituitary", "Malignant Adrenocorticotropin Producing Neoplasm of Pituitary Gland", "malignant adrenocorticotropin producing neoplasm of pituitary gland", "Malignant Adrenocorticotropin Producing Tumor of the Pituitary Gland", "malignant adrenocorticotropin producing tumor of the pituitary gland", "malignant adrenocorticotropin producing neoplasm of the pituitary gland", "Malignant Adrenocorticotropin Producing Neoplasm of the Pituitary Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ACTH-producing pituitary gland carcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C5206453", "names": ["Stage IIIC2 Cervical Cancer FIGO 2018", "Stage IIIC2 Cervical Carcinoma FIGO 2018"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC2 Cervical Cancer FIGO 2018", "shortest_name_length": 37}
{"curie": "MONDO:0012858", "names": ["HACD59", "CD59 Deficiency", "CD59 deficiency", "CD59 DEFICIENCY", "primary CD59 deficiency", "HEMOLYTIC ANEMIA, CD59-MEDIATED, WITH OR WITHOUT IMMUNE-MEDIATED POLYNEUROPATHY", "hemolytic anemia, CD59-mediated, with or without immune-mediated polyneuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary CD59 deficiency", "shortest_name_length": 6}
{"curie": "MONDO:0015798", "names": ["IMT", "Plasma Cell Granuloma", "Plasma cell granuloma", "myofibroblastic tumor", "Myofibroblastic tumor", "plasma cell granuloma", "Myofibroblastic tumour", "myofibroblastic tumors", "Plasma Cell Granulomas", "Granuloma, Plasma Cell", "myofibroblastic tumour", "Plasma cell pseudotumor", "Granulomas, Plasma Cell", "pseudotumor inflammatory", "Inflammatory pseudotumor", "inflammatory pseudotumor", "Plasma cell pseudotumour", "Inflammatory Pseudotumor", "Pseudotumor, inflammatory", "inflammatory fibrosarcoma", "Pseudotumor, Inflammatory", "Inflammatory Fibrosarcoma", "Inflammatory Pseudotumors", "inflammatory pseudotumour", "inflammatory pseudotumors", "Inflammatory pseudotumour", "Pseudotumors, Inflammatory", "Inflammatory myofibroblastic tumor", "inflammatory myofibroblastic tumor", "Inflammatory Myofibroblastic Tumor", "Inflammatory myofibroblastic tumour", "inflammatory myofibroblastic neoplasm", "Inflammatory Myofibroblastic Neoplasm", "Inflammatory myofibroblastic tumor (disorder)", "Plasma cell granuloma (morphologic abnormality)", "Myofibroblastic tumor (morphologic abnormality)", "Inflammatory pseudotumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory myofibroblastic tumor", "shortest_name_length": 3}
{"curie": "UMLS:C0856151", "names": ["Fat redistribution", "fat redistribution"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fat redistribution", "shortest_name_length": 18}
{"curie": "MONDO:0043283", "names": ["Haematite lung", "siderosilicosis", "silicosiderosis", "Silicosiderosis", "Siderosilicosis", "Iron miners lung", "iron miners lung", "iron-miner's lung", "Haematite miners' lung", "Hematite pneumoconiosis", "hematite pneumoconiosis", "Haematite pneumoconiosis", "Siderosilicosis (disorder)", "siderosilicosis (diagnosis)", "Hematite miners' lung disease", "Hematite miner's lung disease", "hematite miners' lung disease", "pneumoconiosis due to hematite", "Haematite miners' lung disease", "Haematite foundry workers' lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "silicosiderosis", "shortest_name_length": 14}
{"curie": "UMLS:C1518742", "names": ["Ovarian Stromal Hyperplasia", "Ovarian stromal hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian stromal hyperplasia", "shortest_name_length": 27}
{"curie": "UMLS:C0393688", "names": ["Opercular Epilepsy", "Opercular epilepsy", "Epilepsy, Opercular", "Opercular Epilepsies", "Opercular epilepsy (disorder)", "Opercular epilepsy (diagnosis)", "frontal lobe epilepsy opercular"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epilepsy, Opercular", "shortest_name_length": 18}
{"curie": "UMLS:C1707447", "names": ["Breast Columnar Cell Hyperplasia with Atypia", "Columnar Cell Hyperplasia of Breast with Atypia", "Columnar Cell Hyperplasia of the Breast with Atypia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Columnar Cell Hyperplasia with Atypia", "shortest_name_length": 44}
{"curie": "MONDO:0012401", "names": ["CSCD", "Witschel dystrophy", "Congenital stromal corneal dystrophy", "congenital stromal corneal dystrophy", "CONGENITAL STROMAL CORNEAL DYSTROPHY", "Congenital Stromal Corneal Dystrophy", "corneal dystrophy, congenital stromal", "Corneal Dystrophy, Congenital Stromal", "CORNEAL DYSTROPHY, CONGENITAL STROMAL", "congenital hereditary stromal dystrophy", "Congenital hereditary stromal dystrophy", "Congenital Stromal Dystrophy of the Cornea", "Dystrophia corneae parenchymatosa congenita", "Dystrophia Corneae Parenchymatosa Congenita", "Congenital stromal corneal dystrophy (disorder)", "Congenital Hereditary Stromal Dystrophy of the Cornea", "Decorin associated congenital stromal corneal dystrophy", "Decorin-Associated Congenital Stromal Corneal Dystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital stromal corneal dystrophy", "shortest_name_length": 4}
{"curie": "UMLS:C4521817", "names": ["Stage IVC Appendix Cancer", "Stage IVC Appendix Carcinoma AJCC v8", "Stage IVC Appendiceal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Appendix Carcinoma AJCC v8", "shortest_name_length": 25}
{"curie": "UMLS:C0862216", "names": ["Mycosis fungoides/Sezary syndrome stage II", "stage II mycosis fungoides/Sezary syndrome", "mycosis fungoides/Sezary syndrome, stage II", "Stage II Mycosis Fungoides and Sezary Syndrome", "Stage II Mycosis Fungoides and Sézary Syndrome", "stage II mycosis fungoides and the Sezary syndrome", "Stage II Mycosis Fungoides and Sezary Syndrome AJCC v7", "Stage II Mycosis Fungoides and Sézary Syndrome AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mycosis fungoides/Sezary syndrome stage II", "shortest_name_length": 42}
{"curie": "MONDO:0012138", "names": ["MDC1D", "MDDGB6", "congenital muscular dystrophy type 1D", "Muscular Dystrophy, Congenital, Type 1D", "muscular dystrophy, congenital, type 1D", "MUSCULAR DYSTROPHY, CONGENITAL, TYPE 1D", "congenital muscular dystrophy large-related", "congenital muscular dystrophy LARGE-related", "muscular dystrophy-dystroglycanopathy type B6", "muscular dystrophy, congenital, large-related", "MUSCULAR DYSTROPHY, CONGENITAL, LARGE-RELATED", "muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 6", "muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B, 6", "muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH IMPAIRED INTELLECTUAL DEVELOPMENT), TYPE B, 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy-dystroglycanopathy type B6", "shortest_name_length": 5}
{"curie": "MONDO:0017112", "names": ["isolated unilateral hemispheric cerebellar hypoplasia", "Isolated unilateral hemispheric cerebellar hypoplasia", "Isolated unilateral hemispheric cerebellar hypoplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated unilateral hemispheric cerebellar hypoplasia", "shortest_name_length": 53}
{"curie": "UMLS:C1336862", "names": ["Anaplastic Parotid Carcinoma", "Anaplastic Carcinoma of Parotid", "Anaplastic Parotid Gland Carcinoma", "Anaplastic Carcinoma of the Parotid", "Undifferentiated Carcinoma of Parotid", "Anaplastic Carcinoma of Parotid Gland", "Undifferentiated Parotid Gland Carcinoma", "Parotid Gland Undifferentiated Carcinoma", "Anaplastic Carcinoma of the Parotid Gland", "Undifferentiated Carcinoma of the Parotid", "Undifferentiated Carcinoma of Parotid Gland", "Undifferentiated Carcinoma of the Parotid Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parotid Gland Undifferentiated Carcinoma", "shortest_name_length": 28}
{"curie": "UMLS:C0026509", "names": ["Closed Monteggia fracture", "Closed Monteggia's fracture", "Closed Monteggia's Fracture", "closed Monteggia's fracture", "Fracture Monteggia's, closed", "Closed Monteggia's fracture (disorder)", "closed Monteggia's fracture (diagnosis)", "closed proximal fracture of ulna (Monteggia's fracture)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Closed Monteggia's fracture", "shortest_name_length": 25}
{"curie": "UMLS:C5447479", "names": ["Advanced Malignant Thoracic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Malignant Thoracic Neoplasm", "shortest_name_length": 36}
{"curie": "UMLS:C0852922", "names": ["Crohn's aggravated", "Crohns disease aggravated", "Crohn's disease aggravated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Crohn's aggravated", "shortest_name_length": 18}
{"curie": "MONDO:0024290", "names": ["enuresis", "ENURESIS", "Enuresis", "Enuresis NOS", "Enuresis, NOS", "enuresis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "enuresis", "shortest_name_length": 8}
{"curie": "MONDO:0017110", "names": ["isolated Dandy-Walker malformation with hydrocephalus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated Dandy-Walker malformation with hydrocephalus", "shortest_name_length": 53}
{"curie": "MONDO:0003462", "names": ["Papillary Adenofibroma", "papillary adenofibroma", "Papillary adenofibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papillary adenofibroma", "shortest_name_length": 22}
{"curie": "MONDO:0014054", "names": ["LPFS2", "CD27 deficiency", "CD27 DEFICIENCY", "lymphoproliferative syndrome 2", "LYMPHOPROLIFERATIVE SYNDROME 2", "CD27 lymphoproliferative syndrome", "lymphoproliferative syndrome type 2", "Combined immunodeficiency due to CD27 deficiency", "lymphoproliferative syndrome caused by mutation in CD27", "Autosomal recessive lymphoproliferative disease due to CD27 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphoproliferative syndrome 2", "shortest_name_length": 5}
{"curie": "UMLS:C0278692", "names": ["Regional Neuroblastoma", "regional neuroblastoma", "neuroblastoma, regional"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Regional Neuroblastoma", "shortest_name_length": 22}
{"curie": "MONDO:0002923", "names": ["Uterine Corpus ESS", "uterine corpus ess", "uterine corpus endometrial stromal tumor", "Uterine Corpus Endometrial Stromal Sarcoma", "uterine corpus endometrial stromal sarcoma", "body of uterus endometrial stromal sarcoma", "body of uterus endometrioid stromal sarcoma", "endometrioid stromal sarcoma of body of uterus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine corpus endometrial stromal sarcoma", "shortest_name_length": 18}
{"curie": "UMLS:C1720797", "names": ["Chronic Bacterial Prostatitis", "chronic bacterial prostatitis", "Bacterial Prostatitis, Chronic", "Chronic Bacterial Prostatitides", "Bacterial Prostatitides, Chronic", "Prostatitides, Chronic Bacterial", "chronic bacterial prostatitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic Bacterial Prostatitis", "shortest_name_length": 29}
{"curie": "MONDO:0014958", "names": ["HAYOS", "Harel-Yoon syndrome", "Harel Yoon syndrome", "HAREL-YOON SYNDROME", "Harel-Yoon syndrome; HAYOS", "Ocular anomalies-axonal neuropathy-developmental delay syndrome", "optic atrophy-peripheral neuropathy-developmental delay syndrome", "Ocular anomalies, axonal neuropathy, developmental delay syndrome", "Ocular anomalies, axonal neuropathy, developmental delay syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Harel-Yoon syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0056802", "names": ["bursopathy", "Bursa disorder", "bursa; disorder", "Bursal disorders", "Bursal Disorders", "disorder of bursa", "Disorder of bursa", "Disorder of bursa, NOS", "Unspecified bursopathy", "bursopathy (diagnosis)", "synovial bursa disorder", "Bursopathy, unspecified", "disease of synovial bursa", "disorder of synovial bursa", "Disorder of bursa (disorder)", "disease (or disorder); bursa", "synovial bursa disease or disorder", "disease or disorder of synovial bursa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "synovial bursa disorder", "shortest_name_length": 10}
{"curie": "UMLS:C1696702", "names": ["anastomotic leak pharynx", "Pharyngeal anastomotic leak", "Pharyngeal Anastomotic Leakage", "Pharyngeal anastomotic leak (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pharyngeal Anastomotic Leakage", "shortest_name_length": 24}
{"curie": "UMLS:C5420843", "names": ["Nodular and Massive Retinal Gliosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nodular and Massive Retinal Gliosis", "shortest_name_length": 35}
{"curie": "MONDO:0012129", "names": ["LACH", "leukoencephalopathy, arthritis, colitis, and hypogammaglobulinema", "LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA", "Leukoencephalopathy, Arthritis, Colitis, and Hypogammaglobulinema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukoencephalopathy, arthritis, colitis, and hypogammaglobulinema", "shortest_name_length": 4}
{"curie": "MONDO:0000302", "names": ["basidiobolomycosis", "Basidiobolomycosis", "infection; Basidiobolus", "Basidiobolus; infection", "Infection by Basidiobolus", "infection by Basidiobolus", "Basidiobolomycosis (diagnosis)", "Infection by Basidiobolus, NOS", "Basidiobolus infectious disease", "infection caused by Basidiobolus", "Infection caused by Basidiobolus", "Basidiobolus disease or disorder", "Basidiobolus caused disease or disorder", "Infection caused by Basidiobolus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "basidiobolomycosis", "shortest_name_length": 18}
{"curie": "MONDO:0009499", "names": ["KRB", "GCL", "GLD", "Krabbe", "disease krabbe", "Krabbe Disease", "Krabbe disease", "krabbe disease", "KRABBE DISEASE", "GALC DEFICIENCY", "krabbes disease", "GALC Deficiency", "diseases krabbe", "Krabbes Disease", "GALC deficiency", "disease krabbes", "krabbe's disease", "Krabbe disease 1", "Deficiency, GALC", "Krabbe's disease", "Krabbe's Disease", "GALC Deficiencies", "Deficiencies, GALC", "psychosine lipidosis", "Psychosine Lipidosis", "leukodystrophy krabbe", "Krabbe leucodystrophy", "Krabbe leukodystrophy", "Krabbe Leukodystrophy", "Krabbe disease (KD) 1", "krabbe leukodystrophy", "Krabbes Leukodystrophy", "Leukodystrophy, Krabbe", "globoid cell sclerosis", "Globoid Leukodystrophy", "Globoid leukodystrophy", "globoid leukodystrophy", "Krabbe's Leukodystrophy", "globoid body; sclerosis", "sclerosis; globoid body", "Leukodystrophy, Globoid", "krabbe's leukodystrophy", "Krabbe's leukodystrophy", "Infantile Krabbe disease", "Globoid Leukodystrophies", "Leukodystrophy, Krabbe's", "Leukodystrophies, Globoid", "Krabbe disease (diagnosis)", "Krabbe disease, early-onset", "Globoid Cell Leukodystrophy", "GLOBOID CELL LEUKODYSTROPHY", "Globoid cell leucodystrophy", "globoid cell leukodystrophy", "Globoid cell leukodystrophy", "Leukodystrophy, Globoid Cell", "Galactosylceramide lipidosis", "Leukodystrophy, globoid cell", "LEUKODYSTROPHY, GLOBOID CELL", "Cell Leukodystrophy, Globoid", "Leukodystrophy, Globoid cell", "galactosylceramide lipidosis", "Galactosylceramide Lipidosis", "Krabbe disease, classic form", "galactosylceramide deficiency", "GALACTOSYL CERAMIDE LIPIDOSIS", "Globoid Cell Leukodystrophies", "Diffuse Globoid Body Sclerosis", "BRAIN, SCLEROSIS, GLOBOID CELL", "Cell Leukodystrophies, Globoid", "diffuse globoid body sclerosis", "Leukodystrophies, Globoid Cell", "Diffuse globoid body sclerosis", "Galactocerebrosidase deficiency", "galactocerebrosidase deficiency", "globoid cell cerebral sclerosis", "Globoid Body Sclerosis, Diffuse", "galactosylsphingosine lipidosis", "Galactocerebrosidase Deficiency", "galactosylceramidase deficiency", "Galactosylsphingosine Lipidosis", "Galactosylceramidase deficiency", "GALACTOCEREBROSIDASE DEFICIENCY", "GLOBOID CELL LEUKOENCEPHALOPATHY", "globoid cell leukoencephalopathy", "Globoid Cell Leukoencephalopathy", "Deficiency, Galactocerebrosidase", "Leukoencephalopathy, Globoid Cell", "Cell Leukoencephalopathy, Globoid", "Galactocerebrosidase Deficiencies", "GCL - Globoid cell leucodystrophy", "Globoid Cell Leukoencephalopathies", "Deficiencies, Galactocerebrosidase", "Galactosylcerebrosidase Deficiency", "Cell Leukoencephalopathies, Globoid", "Leukoencephalopathies, Globoid Cell", "Classic Globoid Cell Leukodystrophy", "beta galactocerebrosidase deficiency", "Leukodystrophy, Globoid Cell, Classic", "Infantile Globoid Cell Leukodystrophy", "galactocerebrosidase (GALC) deficiency", "globoid cell leukodystrophy (GCL, GLD)", "diffuse globoid cell cerebral sclerosis", "Leukodystrophy, Globoid Cell, Infantile", "Galactosylceramidase Deficiency Disease", "Early Onset Globoid Cell Leukodystrophy", "Early-Onset Globoid Cell Leukodystrophy", "Diffuse globoid cell cerebral sclerosis", "Galactosylceramidase Deficiency Diseases", "Globoid cell leukodystrophy, early onset", "Disease, Galactosylceramidase Deficiency", "Deficiency Disease, Galactosylceramidase", "Leukodystrophy, Globoid Cell, Early-Onset", "Diseases, Galactosylceramidase Deficiency", "Deficiency Diseases, Galactosylceramidase", "Familial infantile diffuse brain sclerosis", "galactosylceramide Beta-galactosidase deficiency", "Galactosylceramide beta Galactosidase Deficiency", "Galactosylceramide beta-Galactosidase Deficiency", "Galactosylceramide beta-galactosidase deficiency", "Galactosylceramide Beta-Galactosidase Deficiency", "GALACTOSYLCERAMIDE BETA-GALACTOSIDASE DEFICIENCY", "galactosylceramide beta-galactosidase deficiency", "Galactocerebroside beta-galactosidase deficiency", "Deficiency, Galactosylceramide beta-Galactosidase", "beta-Galactosidase Deficiency, Galactosylceramide", "Galactosylceramide beta-Galactosidase Deficiencies", "Globoid cell leukodystrophy, early onset (disorder)", "beta-Galactosidase Deficiencies, Galactosylceramide", "Deficiencies, Galactosylceramide beta-Galactosidase", "Galactosylceramide beta Galactosidase Deficiency Disease", "Galactosylceramide-beta-Galactosidase Deficiency Disease", "Deficiency Disease, Galactosylceramide-beta-Galactosidase", "Disease, Galactosylceramide-beta-Galactosidase Deficiency", "Galactosylceramide-beta-Galactosidase Deficiency Diseases", "Diseases, Galactosylceramide-beta-Galactosidase Deficiency", "Deficiency Diseases, Galactosylceramide-beta-Galactosidase", "Galactosylceramide beta-galactosidase deficiency (disorder)", "Galactocerebroside beta-galactosidase deficiency - early onset", "Galactocerebroside beta-galactosidase deficiency - early onset (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Krabbe disease", "shortest_name_length": 3}
{"curie": "MONDO:8000011", "names": ["NID A", "VSCN1", "visceral neuropathy familial", "neuronal intestinal dysplasia type A", "NEURONAL INTESTINAL DYSPLASIA, TYPE A", "neuronal intestinal dysplasia, type a", "Neuronal intestinal dysplasia, type A", "Neuronal intestinal pseudoobstruction", "Argyrophil myenteric plexus deficiency of", "Argyrophil myenteric plexus, deficiency of", "ARGYROPHIL MYENTERIC PLEXUS, DEFICIENCY OF", "visceral neuropathy, familial, autosomal recessive", "Visceral Neuropathy, Familial, Autosomal Recessive", "intestinal pseudoobstruction due to neuronal disease", "INTESTINAL PSEUDOOBSTRUCTION DUE TO NEURONAL DISEASE", "Intestinal pseudoobstruction due to neuronal disease", "visceral neuropathy, familial, 1, autosomal recessive", "VISCERAL NEUROPATHY, FAMILIAL, 1, AUTOSOMAL RECESSIVE", "pseudoobstruction chronic idiopathic intestinal neuronal type", "Pseudoobstruction, chronic idiopathic intestinal, neuronal type", "pseudoobstruction, chronic idiopathic intestinal, neuronal type", "PSEUDOOBSTRUCTION, CHRONIC IDIOPATHIC INTESTINAL, NEURONAL TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "visceral neuropathy, familial, 1, autosomal recessive", "shortest_name_length": 5}
{"curie": "MONDO:0012115", "names": ["IS3", "SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3", "scoliosis, isolated, susceptibility to, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scoliosis, isolated, susceptibility to, 3", "shortest_name_length": 3}
{"curie": "UMLS:C0149866", "names": ["Chemical Conjunctivitis", "chemical conjunctivitis", "Chemical conjunctivitis", "CONJUNCTIVITIS, CHEMICAL", "Neonatal Chemical Conjunctivitis", "chemical conjunctivitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chemical conjunctivitis", "shortest_name_length": 23}
{"curie": "UMLS:C4552766", "names": ["miscarriage", "MISCARRIAGE", "Miscarriage", "miscarriages", "Miscarriages", "Miscarriage NOS", "Early fetal demise", "Spontaneous Abortion", "Spontaneous abortion", "pregnancy miscarriage", "miscarriage pregnancy", "miscarriages pregnancy", "Miscarriage (disorder)", "Miscarriage of pregnancy", "miscarriage of pregnancy", "Vaginal expulsion of fetus", "Vaginal expulsion of foetus", "Vaginal expulsion of product of conception"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Miscarriage", "shortest_name_length": 11}
{"curie": "MONDO:0010490", "names": ["CDGIy", "CDG1Y", "CDG2E", "CDG IY", "CDG 1Y", "CDG-Iy", "CDG Iy", "CDG IIe", "CDGIIde", "SSR4-CDG", "COG7-CDG", "CDG syndrome type Iy", "CDG syndrome type IIe", "congenital disorder of glycosylation 1y", "congenital disorder of glycosylation Iy", "SSR4-congenital disorder of glycosylation", "congenital disorder of glycosylation type Iy", "congenital disorder of glycosylation type 1y", "Congenital disorder of glycosylation type Iy", "Congenital disorder of glycosylation type 1y", "congenital disorder of glycosylation type IIe", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iy", "congenital disorder of glycosylation, type Iy", "carbohydrate deficient glycoprotein syndrome type Iy", "Carbohydrate deficient glycoprotein syndrome type Iy", "Carbohydrate deficient glycoprotein syndrome type IIe", "Congenital disorder of glycosylation type 1y (disorder)", "Congenital disorder of glycosylation type 1y (diagnosis)", "congenital disorder of glycosylation, type Iy, X-linked recessive", "Signal sequence receptor subunit 4 congenital disorder of glycosylation", "SSR4-CDG - signal sequence receptor subunit 4 congenital disorder of glycosylation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SSR4-congenital disorder of glycosylation", "shortest_name_length": 5}
{"curie": "UMLS:C3838808", "names": ["Chondrosarcoma, Grade 3", "Chondrosarcoma, grade 3", "Grade III Chondrosarcoma", "High Grade Chondrosarcoma", "High-Grade Chondrosarcoma", "Chondrosarcoma, grade 3 (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chondrosarcoma, grade 3", "shortest_name_length": 23}
{"curie": "MONDO:0002280", "names": ["Anemia", "ANEMIA", "anemia", "ANAEMIA", "Anemias", "anemias", "anaemia", "Anaemia", "anaemias", "Anemia NOS", "Anaemia NOS", "Anemia, NOS", "Hb decreased", "Anaemia, NOS", "Hemoglobin low", "Low hemoglobin", "low hemoglobin", "hemoglobin low", "low haemoglobin", "drop hemoglobin", "Absolute anemia", "Haemoglobin low", "hemoglobin; low", "HEMOGLOBIN DROP", "hemoglobin drop", "hemoglobins low", "haemoglobin low", "low; hemoglobin", "Absolute anaemia", "anemia (disease)", "anemia; essential", "Anemia (disorder)", "anemia (phenotype)", "anemia (diagnosis)", "Unspecified anemia", "Drop in hemoglobin", "Anemia, unspecified", "Unspecified anaemia", "Anemia; unspecified", "HEMOGLOBIN DECREASED", "Anaemia, unspecified", "decreased hemoglobin", "Decreased hemoglobin", "Hemoglobin decreased", "Hemoglobin Decreased", "Decreased haemoglobin", "HAEMOGLOBIN DECREASED", "Haemoglobin decreased", "Decrease in hemoglobin", "Hemoglobin below reference range", "Haemoglobin below reference range", "Hemoglobin below reference range (finding)", "Low number of red blood cells or hemoglobin", "Low number of red blood cells or haemoglobin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anemia", "shortest_name_length": 6}
{"curie": "UMLS:C3900099", "names": ["Mixed Glioma", "Adult Mixed Glioma", "adult mixed glioma", "mixed glioma, adult", "adult gliomas, mixed", "adult oligoastrocytoma", "adult mixed glial tumors", "adult glial tumors, mixed", "adult tumors, mixed glial", "adult anaplastic oligoastrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Mixed Glioma", "shortest_name_length": 12}
{"curie": "UMLS:C4288374", "names": ["Prevertebral Abscess"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prevertebral Abscess", "shortest_name_length": 20}
{"curie": "MONDO:0020706", "names": ["OADIP", "DIPOA", "Heberden's node", "Heberden's Node", "tuberculum arthriticum", "Tuberculum Arthriticum", "Osteoarthritis of distal interphalangeal joint", "OSTEOARTHRITIS OF DISTAL INTERPHALANGEAL JOINTS", "Osteoarthritis of the distal interphalangeal joint", "Osteoarthritis of distal interphalangeal joint (disorder)", "Degenerative joint disease of distal interphalangeal joint"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Heberden's node", "shortest_name_length": 5}
{"curie": "UMLS:C3274310", "names": ["Tracheal web", "Tracheal Web"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tracheal web", "shortest_name_length": 12}
{"curie": "MONDO:0004637", "names": ["aryepiglottic fold cancer", "cancer of aryepiglottic fold", "malignant aryepiglottic fold neoplasm", "malignant neoplasm of aryepiglottic fold", "Malignant tumor aryepiglottic fold - hypopharyngeal aspect", "malignant tumor aryepiglottic fold - hypopharyngeal aspect", "Malignant tumour aryepiglottic fold - hypopharyngeal aspect", "Malignant neoplasm of aryepiglottic fold, hypopharyngeal aspect", "Malignant neoplasm of hypopharyngeal aspect of aryepiglottic fold", "malignant neoplasm of hypopharyngeal aspect of aryepiglottic fold", "Malignant tumor aryepiglottic fold - hypopharyngeal aspect (disorder)", "malignant neoplasm of hypopharyngeal aspect of aryepiglottic fold (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aryepiglottic fold cancer", "shortest_name_length": 25}
{"curie": "MONDO:0018630", "names": ["HNPCC", "hnpcc", "Lynch syndrome", "familial nonpolyposis colon cancer", "Familial nonpolyposis colon cancer", "Colon Cancer, Familial Nonpolyposis", "Hereditary Nonpolyposis Colon Cancer", "Hereditary nonpolyposis colon cancer", "hereditary nonpolyposis colon cancer", "Hereditary Non-polyposis Colon Cancer", "hereditary non-polyposis colon cancer", "hereditary nonpolyposis-Lynch syndrome", "Familial nonpolyposis colorectal cancer", "familial nonpolyposis colorectal cancer", "Colorectal Cancer Hereditary Nonpolyposis", "hereditary nonpolyposis colorectal cancer", "Hereditary nonpolyposis colorectal cancer", "Hereditary Nonpolyposis Colorectal Cancer", "colorectal cancer, hereditary nonpolyposis", "HNPCC - hereditary nonpolyposis colon cancer", "hereditary defective mismatch repair syndrome", "Hereditary nonpolyposis colon cancer (disorder)", "Familial Nonpolyposis Colorectal Cancer Syndrome", "hereditary non-polyposis colon cancer (diagnosis)", "Hereditary nonpolyposis colorectal cancer (HNPCC)", "hereditary colorectal endometrial cancer syndrome", "Hereditary Nonpolyposis Colorectal Cancer (HNPCC)", "HNPCC - hereditary nonpolyposis colorectal cancer", "Hereditary Nonpolyposis Colorectal Cancer Syndrome", "colon cancer, hereditary non-polyposis - Lynch syndrome", "familial non-polyposis colon cancer (hMSH2, hMLH1, hPMS1, hPMS2)", "hereditary non-polyposis colon cancer (hMSH2, hMLH1, hPMS1, hPMS2)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary nonpolyposis colon cancer", "shortest_name_length": 5}
{"curie": "MONDO:0020812", "names": ["DENT PULP EXPOSURE", "EXPOSURE DENT PULP", "PULP EXPOSURE DENT", "Dental Pulp Exposure", "Pulp Exposure, Dental", "Exposure, Dental Pulp", "exposure, dental pulp", "Exposure of tooth pulp", "Exposure of tooth pulp (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exposure, dental pulp", "shortest_name_length": 18}
{"curie": "MONDO:0043953", "names": ["Burkholderia Infection", "Burkholderia infection", "infection, Burkholderia", "Burkholderia infections", "Infection, Burkholderia", "Burkholderia Infections", "Infections, Burkholderia", "infections, Burkholderia", "burkholderia infectious disease", "Burkholderia infectious disease", "Burkholderia disease or disorder", "Infection caused by Burkholderia", "infection caused by Burkholderia", "Burkholderia caused disease or disorder", "Infection caused by Burkholderia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "burkholderia infectious disease", "shortest_name_length": 22}
{"curie": "MONDO:0021902", "names": ["APW", "APSD", "AP Window", "AP window", "Aortic septal defect", "aortic septal defect", "Aortopulmonary Window", "aortopulmonary window", "Aortopulmonary window", "aorto-pulmonary window", "aorticopulmonary window", "aortic-pulmonary window", "Aorticopulmonary window", "aorticopulmonary; window", "window; aorticopulmonary", "AP - Aortopulmonary window", "Common aortopulmonary trunk", "APW - Aortopulmonary window", "aortopulmonary septal defect", "Aortopulmonary septal defect", "Aortopulmonary Septal Defect", "defect; aortopulmonary septum", "Aortopulmonary septal anomaly", "Septal Defect, Aortopulmonary", "aortopulmonary septum; defect", "Aortopulmonary Septal Defects", "Aorticopulmonary septal defect", "Aorticopulmonary Septal Defect", "aorticopulmonary septal defect", "Septal Defects, Aortopulmonary", "Aorticopulmonary Septal Defects", "Septal Defect, Aorticopulmonary", "Aortopulmonary window (disorder)", "Septal Defects, Aorticopulmonary", "aorta; septum pulmonary artery absent", "absence; septum aorta - pulmonary artery", "absence; aorta - pulmonary artery, septum", "absence; pulmonary artery - aorta, septum", "aorticopulmonary septal defect (diagnosis)", "connection; pulmonary artery - aorta, base (anomaly)", "connection; base of aorta and pulmonary artery (anomaly)", "closure; incomplete, septum, between aorta and pulmonary artery", "incomplete; closure, septum, between aorta and pulmonary artery"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortopulmonary window", "shortest_name_length": 3}
{"curie": "UMLS:C4763829", "names": ["Metastatic Plasmacytoid Urothelial Carcinoma", "Metastatic Plasmacytoid Urothelial Carcinoma of the Bladder", "Metastatic Infiltrating Bladder Urothelial Carcinoma, Plasmacytoid Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Infiltrating Bladder Urothelial Carcinoma, Plasmacytoid Variant", "shortest_name_length": 44}
{"curie": "UMLS:C0340757", "names": ["Inferior Vena Cava Stenosis", "Inferior vena cava stenosis", "Inferior vena cava stenosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Inferior vena cava stenosis", "shortest_name_length": 27}
{"curie": "MONDO:0015986", "names": ["bilateral renal aplasia", "Bilateral Renal Agenesis", "bilateral renal agenesis", "renal agenesis, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bilateral renal agenesis", "shortest_name_length": 23}
{"curie": "MONDO:0007873", "names": ["Lactic Acidosis, Chronic Adult Form", "LACTIC ACIDOSIS, CHRONIC ADULT FORM", "lactic acidosis, chronic adult form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lactic acidosis, chronic adult form", "shortest_name_length": 35}
{"curie": "MONDO:0011636", "names": ["DBA2", "DIAMOND-BLACKFAN ANEMIA 2", "Diamond-Blackfan Anemia 2", "Diamond-Blackfan anemia 2", "anemia Diamond-Blackfan 2", "Diamond-Blackfan Anemia, 2", "Anemia, Diamond-Blackfan, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diamond-Blackfan anemia 2", "shortest_name_length": 4}
{"curie": "UMLS:C0015333", "names": ["Radiation", "RADIATION EXPOSURE", "radiation exposure", "Radiation Exposure", "EXPOSURE RADIATION", "Radiation exposure", "radiation; exposure", "exposure; radiation", "Exposure, Radiation", "Exposure to radiation", "exposure to radiation", "Exposure to radiation NOS", "Exposure to radiation, NOS", "Exposure to radiation (event)", "Exposure to unspecified radiation", "Exposure to unspecified type of radiation", "[X]Exposure to unspecified type of radiation", "Exposure to unspecified type of radiation, occurrence at unspecified place", "[X]Exposure to unspecified type of radiation, occurrence at unspecified place", "Exposure to unspecified type of radiation as an external cause of morbidity and mortality"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Exposure to radiation", "shortest_name_length": 9}
{"curie": "MONDO:0100376", "names": ["AML, t(9;11)(p22;q23)", "AML, t(9;11)(p21.3;q23.3)", "acute myeloid leukemia, t(9;11)(p21.3;q23.3)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, t(9;11)(p21.3;q23.3)", "shortest_name_length": 21}
{"curie": "MONDO:0043579", "names": ["Enteritis", "enteritis", "ENTERITIS", "enteritides", "Enteritides", "Enteritis NOS", "Enteritis, NOS", "enteritis (diagnosis)", "Small intestine inflammation", "Enteritis of small intestine", "small intestine inflammation", "enteritis of small intestine", "inflammation of small intestine", "Inflammation of small intestine", "Inflammation of small intestine (disorder)", "Enteritis, inflammatory disorder of small intestine", "enteritis, inflammatory disorder of small intestine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "enteritis", "shortest_name_length": 9}
{"curie": "MONDO:0016081", "names": ["Coronaro-cardiac fistula", "coronary arterial fistulas", "coronary arterial malformations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coronary arterial fistulas", "shortest_name_length": 24}
{"curie": "MONDO:0005805", "names": ["Hypodermyiases", "Hypodermyiasis", "hypodermyiasis", "Oestridae infectious disease", "Oestridae disease or disorder", "Oestridae caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypodermyiasis", "shortest_name_length": 14}
{"curie": "UMLS:C1562722", "names": ["Acute cerebellar syndrome", "Acute cerebellar syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute cerebellar syndrome", "shortest_name_length": 25}
{"curie": "UMLS:C2861617", "names": ["acute monoblastic/monocytic leukemia in remission", "Acute monoblastic/monocytic leukemia, in remission", "Acute Monoblastic and Monocytic Leukemia in Remission", "acute monoblastic/monocytic leukemia in remission (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute monoblastic/monocytic leukemia in remission", "shortest_name_length": 49}
{"curie": "MONDO:0002298", "names": ["Skin Glomangioma", "skin glomangioma", "Glomangioma of skin", "glomangioma of skin", "Glomangioma of Skin", "Cutaneous Glomangioma", "cutaneous glomangioma", "glomangioma of the skin", "Glomangioma of the Skin", "zone of skin glomangioma", "Glomangioma of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous glomangioma", "shortest_name_length": 16}
{"curie": "MONDO:0026763", "names": ["HPE13", "holoprosencephaly 13, X-linked", "HOLOPROSENCEPHALY 13, X-LINKED", "holoprosencephaly 13, X-linked, X-linked recessive, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "holoprosencephaly 13, X-linked", "shortest_name_length": 5}
{"curie": "UMLS:C3714239", "names": ["Bmpr1a-Related Juvenile Polyposis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bmpr1a-Related Juvenile Polyposis", "shortest_name_length": 33}
{"curie": "MONDO:0020193", "names": ["lacrimal gland disease", "disease of lacrimal gland", "disorder of lacrimal gland", "secretory apparatus of the lacrimal system anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secretory apparatus of the lacrimal system anomaly", "shortest_name_length": 22}
{"curie": "MONDO:0000271", "names": ["TB salpingitis", "Tuberculous salpingitis", "Salpingeal tuberculosis", "Salpingitis tuberculous", "tuberculous salpingitis", "Fallopian tube tuberculosis", "fallopian tube tuberculosis", "Tuberculosis (TB) salpingitis", "Tuberculous salpingitis (disorder)", "tuberculous salpingitis (diagnosis)", "Mycobacterium tuberculosis salpingitis", "Tuberculous oophoritis and salpingitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tuberculous salpingitis", "shortest_name_length": 14}
{"curie": "UMLS:C4725811", "names": ["Refractory Malignant Mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Malignant Mesothelioma", "shortest_name_length": 33}
{"curie": "UMLS:C1562689", "names": ["Congenital hereditary endothelial dystrophy", "congenital hereditary endothelial dystrophy", "CHED-congenital hereditary endothelial dystrophy", "Congenital hereditary endothelial dystrophy (disorder)", "congenital hereditary endothelial dystrophy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital hereditary endothelial dystrophy", "shortest_name_length": 43}
{"curie": "MONDO:0004127", "names": ["Occult Lung Adenocarcinoma", "occult lung adenocarcinoma", "lung occult adenocarcinoma", "Occult Adenocarcinoma of Lung", "occult adenocarcinoma of lung", "occult adenocarcinoma of the lung", "Occult Adenocarcinoma of the Lung", "Occult adenocarcinoma of the lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung occult adenocarcinoma", "shortest_name_length": 26}
{"curie": "UMLS:C0854986", "names": ["Lung Adenocarcinoma Stage II", "Lung adenocarcinoma stage II", "Adenocarcinoma lung stage II", "Stage II Lung Adenocarcinoma", "Lung Adenocarcinoma, Stage II", "Stage II Adenocarcinoma of Lung", "Adenocarcinoma of lung stage II", "Adenocarcinoma of lung, stage II", "Stage II Adenocarcinoma of the Lung", "Stage II Lung Adenocarcinoma AJCC v7", "Finding of adenocarcinoma of lung, stage II", "Adenocarcinoma of lung, stage II (disorder)", "clinical finding tumor stage adenocarcinoma of lung, stage II", "Finding of adenocarcinoma of lung, stage II (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma of lung, stage II", "shortest_name_length": 28}
{"curie": "MONDO:0009925", "names": ["PXE", "pseudoxanthoma elasticum", "Pseudoxanthoma elasticum", "PSEUDOXANTHOMA ELASTICUM", "elasticum pseudoxanthoma", "Pseudoxanthoma Elasticum", "Gronblad-Strandberg syndrome", "Gronblad Strandberg Syndrome", "Gronblad-Strandberg Syndrome", "PXE, MODIFIER OF SEVERITY OF", "PXE, modifier of severity of", "Gronblad Strandberg syndrome", "GRONBLAD-STRANDBERG SYNDROME", "GROENBLAD-STRANDBERG SYNDROME", "Groenblad-Strandberg Syndrome", "Syndrome, Gronblad-Strandberg", "Groenblad-Strandberg syndrome", "ELASTOSIS DYSTROPHICA SYNDROME", "PXE - Pseudoxanthoma elasticum", "Inherited pseudoxanthoma elasticum", "Pseudoxanthoma elasticum (disorder)", "ELASTORRHEXIS, SYSTEMIC, OF TOURAINE", "pseudoxanthoma elasticum (diagnosis)", "Gronblad-Strandberg-Touraine syndrome", "AR inherited pseudoxanthoma elasticum", "Gronblad-Strandberg syndrome (disorder)", "Inherited pseudoxanthoma elasticum (disorder)", "pseudoxanthoma elasticum, modifier of severity of", "PSEUDOXANTHOMA ELASTICUM, MODIFIER OF SEVERITY OF", "autosomal recessive inherited pseudoxanthoma elasticum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive inherited pseudoxanthoma elasticum", "shortest_name_length": 3}
{"curie": "MONDO:0005060", "names": ["Liposarcoma", "LIPOSARCOMA", "lip sarcoma", "liposarcoma", "liposarcomas", "Liposarcomas", "sarcoma of lip", "Liposarcoma NOS", "Liposarcoma, NOS", "Fibroliposarcoma", "lipomatous cancer", "liposarcoma, malignant", "Liposarcoma morphology", "LIPOSARCOMA, MALIGNANT", "Liposarcoma (disorder)", "Liposarcomas malignant", "liposarcoma (diagnosis)", "Malignant lipomatous tumor", "Malignant lipomatous tumour", "malignant neoplasm lipomatous", "malignant lipomatous neoplasm", "Malignant Lipomatous Neoplasm", "Liposarcoma Not Otherwise Specified", "Malignant lipomatous tumor morphology", "Liposarcoma (morphologic abnormality)", "Malignant lipomatous tumour morphology", "malignant lipomatous neoplasm (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "liposarcoma", "shortest_name_length": 11}
{"curie": "UMLS:C4764040", "names": ["Locally Advanced Unresectable Digestive System Neuroendocrine Neoplasm", "Locally Advanced Unresectable Gastroenteropancreatic Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Unresectable Digestive System Neuroendocrine Neoplasm", "shortest_name_length": 70}
{"curie": "UMLS:C0002950", "names": ["infected aneurysm", "Infected Aneurysm", "Infected Aneurysms", "Aneurysm, Infected", "Infective aneurysm", "aneurysm; infective", "Aneurysms, Infected", "infective; aneurysm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aneurysm, Infected", "shortest_name_length": 17}
{"curie": "UMLS:C0022362", "names": ["Jaw Disease", "jaw disease", "disease jaw", "Jaw disorder", "jaw diseases", "jaw disorder", "Jaw Diseases", "Disease, Jaw", "disorders jaw", "Diseases, Jaw", "Jaws--Diseases", "Disease of jaw", "disorder of jaw", "Disorder of jaw", "Jaw disorder NOS", "Disorders of jaw", "Disease of jaw, NOS", "Diseases of the jaws", "Disorder of jaw (disorder)", "disease (or disorder); jaw", "disorder of jaw (diagnosis)", "Disease of jaws, unspecified", "Disease of mandible and maxilla", "Unspecified disease of the jaws"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jaw Diseases", "shortest_name_length": 11}
{"curie": "UMLS:C3887824", "names": ["Digestive System Dysplasia", "Gastrointestinal dysplasia", "Gastrointestinal Dysplasia", "Gastrointestinal System Dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal dysplasia", "shortest_name_length": 26}
{"curie": "MONDO:0044651", "names": ["early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome", "shortest_name_length": 93}
{"curie": "MONDO:0030058", "names": ["DFNA77", "DEAFNESS, AUTOSOMAL DOMINANT 77", "deafness, autosomal dominant 77", "hearing loss, autosomal dominant 77", "autosomal dominant nonsyndromic deafness 77"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal dominant 77", "shortest_name_length": 6}
{"curie": "UMLS:C1332961", "names": ["Childhood Cerebral Diffuse Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Cerebral Diffuse Astrocytoma", "shortest_name_length": 38}
{"curie": "MONDO:0005349", "names": ["Otosclerosis", "otosclerosis", "otoscleroses", "Otoscleroses", "OTOSCLEROSIS", "Otospongiosis", "otospongiosis", "Otospongioses", "Otosclerosis, NOS", "Other otosclerosis", "Otospongiosis, NOS", "Otosclerosis, other", "Otosclerosis syndrome", "Otospongiosis syndrome", "otosclerosis (disease)", "Otosclerosis (disorder)", "Unspecified otosclerosis", "otosclerosis (diagnosis)", "Otosclerosis, unspecified", "Other otosclerosis, unspecified ear", "Unspecified otosclerosis, unspecified ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "otosclerosis", "shortest_name_length": 12}
{"curie": "UMLS:C5204288", "names": ["Non-Human Papillomavirus-Related Squamous Cell Carcinoma of the Penis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Human Papillomavirus-Related Squamous Cell Carcinoma of the Penis", "shortest_name_length": 69}
{"curie": "MONDO:0011907", "names": ["ACFD", "ACROCAPITOFEMORAL DYSPLASIA", "Acrocapitofemoral Dysplasia", "acrocapitofemoral dysplasia", "Acrocapitofemoral dysplasia", "Acrocapitofemoral dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acrocapitofemoral dysplasia", "shortest_name_length": 4}
{"curie": "UMLS:C0687132", "names": ["drink heavy", "heavy drinking", "drinking heavy", "heavy alcohol use"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heavy drinking", "shortest_name_length": 11}
{"curie": "UMLS:C0014718", "names": ["Intertrigo candida", "Candida intertrigo", "candida intertrigo", "monilial intertrigo", "Flexural candidosis", "Candidal intertrigo", "Monilial intertrigo", "candidal intertrigo", "candidiasis; intertrigo", "intertrigo; candidiasis", "Intertriginous moniliasis", "Moniliasis intertriginous", "CANDIDIASIS INTERTRIGINOUS", "Intertriginous candidiasis", "Candida intertrigo (disorder)", "candidal intertrigo (diagnosis)", "Candida infection of flexural skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Candidal intertrigo", "shortest_name_length": 18}
{"curie": "UMLS:C5554996", "names": ["CDC73-Related Neoplastic Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CDC73-Related Neoplastic Syndrome", "shortest_name_length": 33}
{"curie": "MONDO:0016572", "names": ["central bilateral macrogyria", "Central bilateral macrogyria", "Central bilateral macrogyria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central bilateral macrogyria", "shortest_name_length": 28}
{"curie": "UMLS:C3272818", "names": ["Colorectal Sarcomatoid Carcinoma", "Colorectal Spindle Cell Carcinoma", "Colorectal (Colon or Rectal) Sarcomatoid Cancer", "Colorectal Carcinoma With Sarcomatoid Components"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Sarcomatoid Carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0043479", "names": ["Adenovirus", "adenovirus", "AdV Infection", "adenovirus infection", "Adenovirus Infection", "Adenoviral Infection", "ADENOVIRUS INFECTION", "Adenovirus infection", "Adenovirus Infections", "infection, adenovirus", "adenovirus infections", "Infection, Adenovirus", "Adenoviridae Infection", "infections, adenovirus", "Adenoviridae infection", "Infections, Adenovirus", "infection, Adenoviridae", "Adenoviridae Infections", "Infection, Adenoviridae", "infections, Adenoviridae", "Adenovirus infection NOS", "Infections, Adenoviridae", "Adenovirus infection, NOS", "disease due to adenovirus", "Disease due to Adenovirus", "DISEASES DUE TO ADENOVIRIDAE", "disease caused by adenovirus", "Disease caused by Adenovirus", "Disease due to Adenovirus, NOS", "Adenoviridae infectious disease", "adenoviridae infectious disease", "Adenoviridae disease or disorder", "Adenovirus infection, unspecified", "Disease caused by Adenovirus (disorder)", "Adenoviridae caused disease or disorder", "infection; viral, adenovirus, unspecified nature or site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenoviridae infectious disease", "shortest_name_length": 10}
{"curie": "MONDO:0019713", "names": ["non-syndromic limb hypoplasia", "isolated limb reduction defect", "nonsyndromic limb reduction defect", "non-syndromic limb reduction defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-syndromic limb reduction defect", "shortest_name_length": 29}
{"curie": "MONDO:0003907", "names": ["polyvesicular vitelline pattern ovarian yolk sac tumor", "ovarian yolk sac tumor, polyvesicular vitelline pattern", "Ovarian Yolk Sac Tumor, Polyvesicular Vitelline Pattern"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian yolk sac tumor, polyvesicular vitelline pattern", "shortest_name_length": 54}
{"curie": "MONDO:0018559", "names": ["LUTO", "Fetal lower urinary tract obstruction", "fetal lower urinary tract obstruction", "Foetal lower urinary tract obstruction", "Fetal lower urinary tract obstruction (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fetal lower urinary tract obstruction", "shortest_name_length": 4}
{"curie": "MONDO:0012612", "names": ["MRT12", "Mental Retardation, Autosomal Recessive 12", "mental retardation, autosomal recessive 12", "intellectual disability, autosomal recessive 12", "mental retardation, autosomal recessive type 12", "intellectual disability, autosomal recessive type 12", "autosomal recessive intellectual developmental disorder 12", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 12", "intellectual developmental disorder, autosomal recessive 12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 12", "shortest_name_length": 5}
{"curie": "MONDO:0032759", "names": ["IDDSSA", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH SHORT STATURE AND VARIABLE SKELETAL ANOMALIES", "intellectual developmental disorder with short stature and variable skeletal anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder with short stature and variable skeletal anomalies", "shortest_name_length": 6}
{"curie": "MONDO:0011291", "names": ["CDGIc", "CDG1C", "CDG-Ic", "CDG Ic", "CDG 1C", "ALG6-CDG", "ALG6-CDG1C", "CDGS5, FORMERLY", "CDGS5 (formerly)", "ALG6-CDG (CDG-Ic)", "CDG syndrome type Ic", "glucosyltransferase 1 deficiency", "Glucosyltransferase 1 deficiency", "congenital disorder of glycosylation Ic", "congenital disorder of glycosylation 1c", "ALG6 congenital disorder of glycosylation", "Congenital disorder of glycosylation type Ic", "Congenital disorder of glycosylation type 1C", "Congenital disorder of glycosylation type 1c", "congenital disorder of glycosylation type Ic", "congenital disorder of glycosylation type 1C", "Congenital Disorder of Glycosylation Type Ic", "ALG6-congenital disorder of glycosylation 1C", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ic", "Congenital Disorder Of Glycosylation, Type Ic", "congenital disorder of glycosylation, type Ic", "Carbohydrate deficient glycoprotein syndrome type V", "Carbohydrate-deficient glycoprotein syndrome type V", "Carbohydrate deficient glycoprotein syndrome type Ic", "Carbohydrate deficient glycoprotein syndrome type 1c", "carbohydrate-deficient glycoprotein syndrome type 1C", "carbohydrate deficient glycoprotein syndrome type Ic", "carbohydrate-deficient glycoprotein syndrome, type V", "Congenital disorder of glycosylation type 1c (disorder)", "congenital disorder of glycosylation type Ic (diagnosis)", "CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME, TYPE V, FORMERLY", "carbohydrate-deficient glycoprotein syndrome, type V, formerly", "carbohydrate-deficient glycoprotein syndrome, type V (formerly)", "congenital disorder of glycosylation caused by mutation in ALG6", "carbohydrate-deficient glycoprotein syndrome, type I, with deficient glycosylation of dolichol-linked oligosaccharide", "carbohydrate-deficient glycoprotein syndrome, type 1 with deficient glycosylation of dolichol-linked oligosaccharide (formerly)", "CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME, TYPE I, WITH DEFICIENT GLYCOSYLATION OF DOLICHOL-LINKED OLIGOSACCHARIDE, FORMERLY", "carbohydrate-deficient glycoprotein syndrome, type I, with deficient glycosylation of dolichol-linked oligosaccharide, formerly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ALG6-congenital disorder of glycosylation 1C", "shortest_name_length": 5}
{"curie": "UMLS:C1332343", "names": ["Atrial Paraganglioma", "Paraganglioma of Atrium", "Paraganglioma of the Atrium", "Paraganglioma of Cardiac Atrium", "Paraganglioma of Atrium of Heart", "Paraganglioma of the Cardiac Atrium", "Paraganglioma of the Atrium of the Heart"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atrial Paraganglioma", "shortest_name_length": 20}
{"curie": "UMLS:C0279960", "names": ["Stage I Diffuse Large Cell Lymphoma", "stage I adult diffuse large cell lymphoma", "Adult Diffuse Large Cell Lymphoma Stage I", "Stage I Adult Diffuse Large Cell Lymphoma", "adult diffuse large cell lymphoma, stage I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Adult Diffuse Large Cell Lymphoma", "shortest_name_length": 35}
{"curie": "MONDO:0015905", "names": ["complex dyslipidemia", "Complex dyslipidemia", "syndromic dyslipidemia", "rare syndromic dyslipidemia", "Complex dyslipidemia (disorder)", "syndromic inherited lipid metabolism disorder", "syndrome associated with inherited lipid metabolism disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic dyslipidemia", "shortest_name_length": 20}
{"curie": "MONDO:0024304", "names": ["common ichthyosis", "fish scale disease", "ichthyosis vulgaris", "Ichthyosis Vulgaris"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ichthyosis vulgaris", "shortest_name_length": 17}
{"curie": "UMLS:C5418671", "names": ["CONGESTION/HEMORRHAGE", "Congestion and Hemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congestion and Hemorrhage", "shortest_name_length": 21}
{"curie": "UMLS:C1332203", "names": ["Adult Intracranial Tumor", "Adult Intracranial Neoplasm", "Adult Intracranial Neoplasms"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Intracranial Neoplasm", "shortest_name_length": 24}
{"curie": "UMLS:C3274454", "names": ["Acquired Chylothorax", "Acquired chylothorax", "Acquired chylothorax (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired chylothorax", "shortest_name_length": 20}
{"curie": "MONDO:0007025", "names": ["CHANCRE", "Chancre", "chancre", "chancres", "SYPHILIS CHANCRE", "syphilis chancre", "primary syphilis", "syphilis primary", "Syphilitic chancre", "chancre syphilitic", "chancre; syphilitic", "Chancre, syphilitic", "Syphilitic chancre NOS", "Primary syphilis - chancre", "Syphilitic chancre (diagnosis)", "Chancre caused by Treponema pallidum", "Chancre caused by Treponema pallidum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chancre", "shortest_name_length": 7}
{"curie": "UMLS:C5205253", "names": ["Duodenal NET G2", "Duodenal Neuroendocrine Tumor G2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Duodenal Neuroendocrine Tumor G2", "shortest_name_length": 15}
{"curie": "MONDO:0007256", "names": ["LCC", "HCC", "LIHC", "hepatoma", "Hepatoma", "HEPATOMA", "Hepatomas", "hepatomas", "liver cancer", "Hepatoma, NOS", "hepatoblastoma", "adult hepatoma", "Carcinoma liver", "HEPATOCARCINOMA", "CARCINOMA LIVER", "Hepatocarcinoma", "liver carcinoma", "Liver carcinoma", "hepatocarcinoma", "LIVER CARCINOMA", "liver cell cancer", "hepatic carcinoma", "Hepatic Carcinoma", "Carcinoma of liver", "carcinoma of liver", "Malignant hepatoma", "Adult Liver Cancer", "CARCINOMA OF LIVER", "Adult Liver Cancers", "Liver Cancer, Adult", "Hepatoma, malignant", "Cancer, Adult Liver", "LIVER CELL CARCINOMA", "Liver Cell Carcinoma", "Cancers, Adult Liver", "Liver Cancers, Adult", "liver cell carcinoma", "Liver cell carcinoma", "Liver Cell Carcinomas", "hepatocellular cancer", "Carcinoma, Liver Cell", "Hepatocellular Cancer", "Cell Carcinoma, Liver", "Hepatic cell carcinoma", "Cell Carcinomas, Liver", "Carcinomas, Liver Cell", "cancer, hepatocellular", "Carcinoma of liver cell", "Primary hepatocarcinoma", "Primary liver carcinoma", "carcinoma; hepatic cell", "hepatic cell; carcinoma", "hepatoblastoma, somatic", "carcinoma of liver cells", "Hepatocellular carcinoma", "Hepatocellular Carcinoma", "HEPATOCELLULAR CARCINOMA", "Carcinoma hepatocellular", "hepatocellular carcinoma", "Carcinoma of Liver Cells", "hepatocellular; carcinoma", "carcinoma; hepatocellular", "Carcinoma, Hepatocellular", "Hepatocellular Carcinomas", "LIVER, CARCINOMA, PRIMARY", "LCC - Liver cell carcinoma", "Carcinomas, Hepatocellular", "Primary carcinoma of liver", "Primary malignant hepatoma", "Liver Cell Carcinoma, Adult", "carcinoma of the liver cells", "Primary liver cell carcinoma", "Carcinoma of the Liver Cells", "Hepatocellular carcinoma NOS", "hepatocellular adenocarcinoma", "Hepatocellular carcinoma, NOS", "LIVER CANCER, HEPATOCARCINOMA", "carcinoma of liver (diagnosis)", "HCC - Hepatocellular carcinoma", "hepatocellular cancer, somatic", "Liver cell carcinoma (disorder)", "Primary Carcinoma of Liver Cells", "primary carcinoma of liver cells", "Primary hepatocellular carcinoma", "hepatocellular carcinoma of liver", "hepatocellular carcinoma, somatic", "liver neoplasm malignant carcinoma", "CARCINOMA, HEPATOCELLULAR, MALIGNANT", "Primary Carcinoma of the Liver Cells", "carcinoma, hepatocellular, malignant", "primary carcinoma of the liver cells", "Primary carcinoma of liver (disorder)", "adult primary hepatocellular carcinoma", "Primary carcinoma of liver (diagnosis)", "Primary liver cell carcinoma (disorder)", "Increased hepatocellular carcinoma risk", "Carcinoma of liver, specified as primary", "Hepatoblastoma Caused By Somatic Mutation", "HEPATOBLASTOMA CAUSED BY SOMATIC MUTATION", "hepatoblastoma caused by somatic mutation", "Liver and Intrahepatic bile duct carcinoma", "Increased risk of hepatocellular carcinoma", "liver neoplasm malignant carcinoma primary", "liver and intrahepatic bile duct carcinoma", "liver cell cancer (hepatocellular carcinoma)", "Liver Cell Cancer (Hepatocellular Carcinoma)", "hepatocellular carcinoma of liver (diagnosis)", "Increased incidence of hepatocellular carcinoma", "hepatocellular carcinoma, childhood type, somatic", "Hepatocellular carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatocellular carcinoma", "shortest_name_length": 3}
{"curie": "MONDO:0008908", "names": ["CDG2A", "CDGS2", "CDG 2A", "CDGIIA", "CDGIIa", "CDG IIA", "CDG-IIa", "CDG IIa", "MGAT2-CDG", "CDGS2, FORMERLY", "ALKURAYA SYNDROME", "Alkuraya syndrome", "MGAT2-CDG (CDG-IIa)", "CDG syndrome type IIa", "MGAT2-congenital disorder of glycosylation", "Congenital disorder of glycosylation type 2a", "Congenital disorder of glycosylation type 2A", "N-acetylglucosaminyltransferase 2 deficiency", "congenital disorder of glycosylation type 2a", "Congenital disorder of glycosylation type IIa", "congenital disorder of glycosylation type IIa", "N-Acetylglucosaminyl transferase II deficiency", "congenital disorder of glycosylation, type IIa", "Congenital Disorder Of Glycosylation, Type IIA", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa", "carbohydrate-deficient glycoprotein syndrome type 2", "carbohydrate-deficient glycoprotein syndrome type II", "Carbohydrate-deficient glycoprotein syndrome type II", "Carbohydrate-deficient glycoprotein syndrome, type 2", "Carbohydrate deficient glycoprotein syndrome type 2a", "Carbohydrate deficient glycoprotein syndrome type IIa", "carbohydrate deficient glycoprotein syndrome type IIa", "carbohydrate-deficient glycoprotein syndrome, type II", "CDG - Carbohydrate-deficient glycoprotein syndrome type II", "Carbohydrate-deficient glycoprotein syndrome type II (disorder)", "Carbohydrate deficient glycoprotein syndrome type 2a (disorder)", "carbohydrate-deficient glycoprotein syndrome, type II, formerly", "CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME, TYPE II, FORMERLY", "carbohydrate-deficient glycoprotein syndrome type II (diagnosis)", "mental retardation, growth retardation, prominent columella, and open mouth", "mental retardation, Growth retardation, prominent columella, and open mouth", "MENTAL RETARDATION, GROWTH RETARDATION, PROMINENT COLUMELLA, AND OPEN MOUTH", "intellectual disability, Growth retardation, prominent columella, and open mouth", "carbohydrate-deficient glycoprotein syndrome, type II, formerly; CDGS2, formerly", "MGAT2-CDG - alpha-1,6-mannosyl-glycoprotein beta-1,2-n-acetylglucosaminyltransferase congenital disorder of glycosylation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MGAT2-congenital disorder of glycosylation", "shortest_name_length": 5}
{"curie": "MONDO:0009659", "names": ["MPS4A", "mps iv", "MPS 4A", "MPSIVA", "MPS IVA", "MPS IV A", "GALNS DEFICIENCY", "GALNS deficiency", "Morquio A Disease", "MORQUIO A DISEASE", "Morquio A disease", "Morquio syndrome A", "Disease, Morquio A", "MORQUIO SYNDROME A", "Morquio A syndrome", "Morquio Syndrome A", "Syndrome A, Morquio", "Morquio disease type A", "Morquio syndrome type A", "mucopolysaccharidosis IVA", "Mucopolysaccharidosis IV-A", "Deficiency of chondroitinase", "Mucopolysaccharidosis type 4A", "mucopolysaccharidosis type 4A", "mucopolysaccharidosis, type 4A", "Mucopolysaccharidosis type IVA", "mucopolysaccharidosis type IVA", "Mucopolysaccharidosis Type IVA", "mucopolysaccharidosis, type IVA", "Mucopolysaccharidosis Type IV A", "Mucopolysaccharidosis, MPS-IV-A", "MUCOPOLYSACCHARIDOSIS, TYPE IVA", "Mucopolysaccharidosis, type IVA", "Morquio's syndrome, classic form", "Galactose-6-sulfatase deficiency", "Galactose-6-sulphatase deficiency", "Deficiency of chondroitinsulfatase", "Morquio syndrome type A (diagnosis)", "Deficiency of chondroitinsulphatase", "MPS IV-A-Mucopolysaccharidosis IV-A", "Galactosamine-6-Sulfatase Deficiency", "galactosamine-6-sulfatase deficiency", "Galactosamine-6-sulfatase deficiency", "GALACTOSAMINE-6-SULFATASE DEFICIENCY", "Galactosamine 6 Sulfatase Deficiency", "Deficiency, Galactosamine-6-Sulfatase", "Galactosamine-6-sulphatase deficiency", "Mucopolysaccharidosis IV-A (disorder)", "Galactosamine-6-Sulfatase Deficiencies", "Deficiencies, Galactosamine-6-Sulfatase", "Deficiency of galactose-6-sulfate sulfatase", "N-acetylgalactosamine-6-sulfatase deficiency", "N-acetylgalactosamine-6-sulphatase deficiency", "Deficiency of galactose-6-sulphate sulphatase", "Deficiency of N-acetylgalactosamine-6-sulfatase", "Deficiency of N-acetylgalactosamine-6-sulphatase", "N-acetylgalactosamine-6-sulfate sulfatase deficiency", "Deficiency of N-acetylgalactosamine-6-sulfatase (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucopolysaccharidosis type 4A", "shortest_name_length": 5}
{"curie": "MONDO:0021581", "names": ["connective tissue tumor", "connective tissue tumors", "connective tissue cancer", "cancers connective tissue", "Connective Tissue Neoplasm", "connective neoplasm tissue", "Connective tissues--Tumors", "Connective tissue neoplasm", "Tumor of connective tissue", "connective tissue neoplasm", "tumor of connective tissue", "Tumour of connective tissue", "Neoplasm, Connective Tissue", "Connective Tissue Neoplasms", "neoplasm, connective tissue", "connective tissue neoplasms", "tumour of connective tissue", "Neoplasms, Connective Tissue", "neoplasm of connective tissue", "neoplasm of connective tissues", "Neoplasm of connective tissues", "Connective tissue neoplasm NOS", "Tumor of mesothelial and soft tissue", "connective tissue neoplasm (disease)", "Tumour of mesothelial and soft tissue", "mesenchymal tissue malignant neoplasm", "Neoplasm of connective tissues (disorder)", "neoplasm of connective tissue (diagnosis)", "Tumor of mesothelial and soft tissue (navigational concept)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "connective tissue neoplasm", "shortest_name_length": 23}
{"curie": "MONDO:0008445", "names": ["Mehes syndrome", "delayed speech-facial asymmetry-strabismus-ear lobe creases syndrome", "Delayed speech-facial asymmetry-strabismus-ear lobe creases syndrome", "delayed speech and facial asymmetry with strabismus and ear lobe skin crease syndrome", "Delayed speech and facial asymmetry with strabismus and ear lobe skin crease syndrome", "delayed speech development, facial asymmetry, strabismus, and transverse ear lobe creases", "Speech Development, Delayed, With Facial Asymmetry, Strabismus, And Transverse Earlobe Crease", "speech development, delayed, with facial asymmetry, strabismus, and transverse earlobe CREASE", "SPEECH DEVELOPMENT, DELAYED, WITH FACIAL ASYMMETRY, STRABISMUS, AND TRANSVERSE EARLOBE CREASE", "Delayed speech and facial asymmetry with strabismus and ear lobe skin crease syndrome (disorder)", "delayed speech and facial asymmetry with strabismus and ear lobe skin crease syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "delayed speech-facial asymmetry-strabismus-ear lobe creases syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C4764050", "names": ["Refractory Cholangiocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Cholangiocarcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0014172", "names": ["SPGF12", "NANOS1 azoospermia", "SPERMATOGENIC FAILURE 12", "spermatogenic failure 12", "spermatogenic failure type 12", "azoospermia caused by mutation in NANOS1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 12", "shortest_name_length": 6}
{"curie": "MONDO:0005858", "names": ["mucinous cystadenocarcinoma", "Mucinous cystadenocarcinoma", "Mucinous Cystadenocarcinoma", "Mucinous Cystadenocarcinomas", "Cystadenocarcinoma, Mucinous", "Pseudomucinous adenocarcinoma", "Cystadenocarcinomas, Mucinous", "Pseudomucinous Adenocarcinoma", "Mucinous cystadenocarcinoma NOS", "Mucinous cystadenocarcinoma, NOS", "Pseudomucinous cystadenocarcinoma", "Pseudomucinous Cystadenocarcinoma", "Pseudomucinous cystadenocarcinoma, NOS", "mucinous; cystadenocarcinoma, unspecified site", "cystadenocarcinoma; mucinous, unspecified site", "cystadenocarcinoma; pseudomucinous, unspecified site", "pseudomucinous; cystadenocarcinoma, unspecified site", "Mucinous cystadenocarcinoma (morphologic abnormality)", "mucinous cystadenocarcinoma (morphologic abnormality)", "mucinous cystadenocarcinoma NOS (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucinous cystadenocarcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C0853847", "names": ["Pathogen resistance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathogen resistance", "shortest_name_length": 19}
{"curie": "MONDO:0035586", "names": ["Cramp-fasciculation syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cramp-fasciculation syndrome", "shortest_name_length": 28}
{"curie": "UMLS:C0149778", "names": ["soft tissue infection", "Soft Tissue Infection", "Soft tissue infection", "infection soft tissue", "SOFT TISSUE INFECTION", "Soft tissue infections", "Soft Tissue Infections", "Infection, Soft Tissue", "soft tissue infections", "infections soft tissue", "Infections, Soft Tissue", "infections soft tissues", "Soft tissue infection NOS", "Soft tissue infection, NOS", "Soft tissue infection (disorder)", "Soft tissue infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Soft Tissue Infection", "shortest_name_length": 21}
{"curie": "UMLS:C5204618", "names": ["Bladder Malignant PEComa", "Bladder Malignant Perivascular Epithelioid Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder Malignant PEComa", "shortest_name_length": 24}
{"curie": "MONDO:0016306", "names": ["Niemann-Pick disease type C, severe perinatal form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Niemann-Pick disease type C, severe perinatal form", "shortest_name_length": 50}
{"curie": "UMLS:C1458156", "names": ["Recurrence", "recurrence", "Recurrent cancer", "Recurrent Cancer", "recurrent cancer", "Recurrent Malignant Tumor", "malignant neoplasm recurrent", "Recurrent Malignant Neoplasm", "Recurrent malignant neoplastic disease", "Recurrent malignant neoplastic disease (disorder)", "Recurrent malignant neoplastic disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Malignant Neoplasm", "shortest_name_length": 10}
{"curie": "UMLS:C0581392", "names": ["Multiple sclerosis exacerbation", "exacerbation multiple sclerosis", "multiple sclerosis exacerbation", "exacerbations multiple sclerosis", "Exacerbation of multiple sclerosis", "exacerbation of multiple sclerosis", "Multiple sclerosis (MS) exacerbation", "Exacerbation of multiple sclerosis (disorder)", "Exacerbation of multiple sclerosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Exacerbation of multiple sclerosis", "shortest_name_length": 31}
{"curie": "UMLS:C0240811", "names": ["PROSTATE INFECTION", "Prostate infection", "infection prostate", "prostate infection", "infections prostate", "infection; prostate", "Prostatic Infection", "prostate; infection", "prostatic infection", "prostatic infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostatic Infection", "shortest_name_length": 18}
{"curie": "UMLS:C3831399", "names": ["Basophilopenia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Basophilopenia", "shortest_name_length": 14}
{"curie": "UMLS:C0268221", "names": ["Fucosidosis Type 1", "Fucosidosis type I", "Fucosidosis Type I", "Fucosidosis, type I", "Type 1, Fucosidosis", "Fucosidosis Type 1s", "Type 1s, Fucosidosis", "Infantile fucosidosis", "Infantile Fucosidosis", "Fucosidosis, Infantile", "Infantile fucosidosis (disorder)", "Fucosidosis, fatal infantile type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fucosidosis Type I", "shortest_name_length": 18}
{"curie": "MONDO:0007377", "names": ["GCDI", "GCD1", "CDGG1", "classic GCD", "Classic GCD", "granular corneal dystrophy 1", "Corneal dystrophy granular type", "corneal dystrophy granular type", "Groenouw type I corneal dystrophy", "Corneal dystrophy Groenouw type I", "Groenouw corneal dystrophy type I", "granular corneal dystrophy type 1", "granular corneal dystrophy type I", "corneal dystrophy Groenouw type I", "Granular corneal dystrophy type I", "Granular corneal dystrophy type 1", "CORNEAL DYSTROPHY, GROENOUW TYPE I", "corneal dystrophy, Groenouw type 1", "Classic granular corneal dystrophy", "corneal dystrophy, Groenouw type I", "classic granular corneal dystrophy", "granular corneal dystrophy, type 1", "GRANULAR CORNEAL DYSTROPHY, TYPE I", "Granular Corneal Dystrophy, Type I", "corneal dystrophy punctate or nodular", "Corneal dystrophy punctate or nodular", "Corneal Dystrophy, Punctate or Nodular", "CORNEAL DYSTROPHY, PUNCTATE OR NODULAR", "corneal dystrophy, punctate or nodular", "Granular corneal dystrophy type I (disorder)", "Groenouw corneal dystrophy type I (disorder)", "Groenouw corneal dystrophy type I (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "granular corneal dystrophy type I", "shortest_name_length": 4}
{"curie": "MONDO:0004862", "names": ["vitreous abscess", "Vitreous abscess", "abscess; vitreous", "vitreous; abscess", "Vitreous abscess (disorder)", "vitreous abscess (diagnosis)", "vitreous abscess endophthalmitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitreous abscess", "shortest_name_length": 16}
{"curie": "MONDO:0021761", "names": ["acral dysostosis dyserythropoiesis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acral dysostosis dyserythropoiesis syndrome", "shortest_name_length": 43}
{"curie": "UMLS:C1656427", "names": ["Early-onset schizophrenia", "early onset schizophrenia", "Early onset schizophrenia", "Early onset schizophrenia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Early onset schizophrenia", "shortest_name_length": 25}
{"curie": "MONDO:0019251", "names": ["oligosaccharidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oligosaccharidosis", "shortest_name_length": 18}
{"curie": "MONDO:0019358", "names": ["Encephalopathy due to sulfite oxidase deficiency", "encephalopathy due to sulfite oxidase deficiency", "Encephalopathy due to sulphite oxidase deficiency", "Encephalopathy due to sulfite oxidase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephalopathy due to sulfite oxidase deficiency", "shortest_name_length": 48}
{"curie": "UMLS:C0155206", "names": ["Eyelid sensory disorder", "Sensory disorder of eyelid", "sensory disorders of eyelid", "Sensory disorders of eyelid", "Sensory disorder of eyelid (disorder)", "sensory disorders of eyelid (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sensory disorder of eyelid", "shortest_name_length": 23}
{"curie": "MONDO:0011421", "names": ["MC5DN1", "mitochondrial complex V deficiency", "Complex 5 mitochondrial respiratory chain deficiency", "mitochondrial Complex 5 (ATP synthase) deficiency, Atpaf2 type", "MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE", "mitochondrial complex V (ATP synthase) deficiency nuclear type 1", "mitochondrial Complex 5 (ATP synthase) deficiency, nuclear type 1", "MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1", "mitochondrial complex V (ATP synthase) deficiency, nuclear type 1", "ATPAF2 mitochondrial proton-transporting ATP synthase complex deficiency", "mitochondrial proton-transporting ATP synthase complex deficiency caused by mutation in ATPAF2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex V (ATP synthase) deficiency, nuclear type 1", "shortest_name_length": 6}
{"curie": "UMLS:C0854977", "names": ["Large cell lung cancer recurrent", "Relapsed Large Cell Lung Carcinoma", "Recurrent Lung Large Cell Carcinoma", "Recurrent Large Cell Lung Carcinoma", "Relapsed Large Cell Carcinoma of Lung", "Recurrent Large Cell Carcinoma of Lung", "Relapsed Large Cell Carcinoma of the Lung", "Recurrent Large Cell Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Large cell lung cancer recurrent", "shortest_name_length": 32}
{"curie": "MONDO:0013635", "names": ["AOS2", "ADAMS-OLIVER SYNDROME 2", "Adams-Oliver syndrome 2", "DOCK6 Adams-Oliver syndrome", "Adams-Oliver syndrome type 2", "Adams-Oliver syndrome caused by mutation in DOCK6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adams-Oliver syndrome 2", "shortest_name_length": 4}
{"curie": "UMLS:C5419397", "names": ["Hepatic or Biliary Problem", "Unspecified Hepatic or Biliary Problem"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatic or Biliary Problem", "shortest_name_length": 26}
{"curie": "UMLS:C0206369", "names": ["Splenoses", "splenosis", "Splenosis", "Splenosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Splenosis", "shortest_name_length": 9}
{"curie": "UMLS:C5206695", "names": ["Locally Advanced Renal Pelvis Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Renal Pelvis Urothelial Carcinoma", "shortest_name_length": 50}
{"curie": "MONDO:0024654", "names": ["Skull Disease", "disease skull", "skull disease", "Skull Disorder", "diseases skull", "skull disorder", "disease of skull", "Disorder of skull", "disorder of skull", "skull disease or disorder", "Disorder of skull (disorder)", "disease or disorder of skull"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skull disorder", "shortest_name_length": 13}
{"curie": "UMLS:C3899121", "names": ["Fetal SGA with Abdominal Circumference Less than Tenth Percentile", "Fetal Small for Gestational Age with Abdominal Circumference Less than Tenth Percentile", "Fetus Small for Gestational Age with Abdominal Circumference Less than Tenth Percentile"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fetus Small for Gestational Age with Abdominal Circumference Less than Tenth Percentile", "shortest_name_length": 65}
{"curie": "MONDO:0006854", "names": ["Mesenchymoma", "mesenchymoma", "Mesenchymomas", "Mesenchymoma NOS", "[M]Mesenchymomas", "Mesenchymoma, NOS", "Mesenchymoma (disorder)", "Mixed mesenchymal tumor", "Mixed mesenchymal tumour", "Mesenchymoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mesenchymoma", "shortest_name_length": 12}
{"curie": "MONDO:0024634", "names": ["large intestine disease", "diseases intestine large", "Large intestine diseases", "disease intestines large", "large intestine disorder", "diseases intestines large", "disorders intestine large", "disease of large intestine", "disorder of large intestine", "Disorder of large intestine", "large intestine disease or disorder", "Disorder of large intestine (disorder)", "disease or disorder of large intestine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "large intestine disorder", "shortest_name_length": 23}
{"curie": "MONDO:0018895", "names": ["Kelly Syndrome", "Kelly-Paterson", "Vinson-Plummer", "Plummer-Vinson", "Kellys Syndrome", "Kelly's Syndrome", "Kelly's syndrome", "Syndrome, Kelly's", "Patterson Syndrome", "Pattersons Syndrome", "Paterson’s syndrome", "Paterson's syndrome", "Patterson's Syndrome", "sideropenic dysphagia", "Syndrome, Patterson's", "Sideropenic dysphagia", "plummer vinson anemia", "DYSPHAGIA, SIDEROPENIC", "sideropenic; dysphagia", "dysphagia sideropenica", "ANEMIA, PLUMMER-VINSON", "dysphagia; sideropenic", "Kelly-Paterson syndrome", "PLUMMER VINSON SYNDROME", "plummer-vinson syndrome", "Paterson-Kelly syndrome", "plummer vinson syndrome", "Plummer-Vinson Syndrome", "Plummer-Vinson syndrome", "Plummer Vinson syndrome", "PLUMMER-VINSON SYNDROME", "paterson-kelly syndrome", "Plummer Vinson Syndrome", "Kelly-Patterson syndrome", "Patterson-Kelly Syndrome", "Syndrome, Plummer Vinson", "Syndrome, Plummer-Vinson", "Patterson Kelly Syndrome", "Syndrome, Patterson-Kelly", "Paterson-Brown-Kelly syndrome", "Brown-Kelly-Paterson syndrome", "PATERSON-BROWN-KELLY SYNDROME", "Brown-Patterson-Kelly syndrome", "Patterson-Brown-Kelly Syndrome", "Patterson Brown Kelly Syndrome", "paterson(-Brown)-Kelly syndrome", "Syndrome, Patterson-Brown-Kelly", "Plummer-Vinson syndrome (disorder)", "Plummer-Vinson syndrome (diagnosis)", "Plummer-Vinson-Patterson-Kelly syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Plummer-Vinson syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C0701826", "names": ["Perinatal death", "PERINATAL DEATH", "Perinatal Death", "perinatal death", "Perinatal Deaths", "Death, Perinatal", "deaths perinatal", "Deaths, Perinatal", "Perinatal Mortality", "Mortality;perinatal", "mortality perinatal", "Perinatal mortality", "perinatal mortality", "Perinatal death, NOS", "PND - Perinatal death", "Perinatal death (event)", "Perinatal mortality, NOS", "perinatal death (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perinatal death", "shortest_name_length": 15}
{"curie": "UMLS:C3146256", "names": ["Stage II Rectal Cancer", "Stage II Rectal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Rectal Cancer AJCC v7", "shortest_name_length": 22}
{"curie": "UMLS:C2987145", "names": ["PanIN-3", "High Grade PanIN", "High-Grade PanIN", "Pancreatic Intraepithelial Neoplasia-3", "Grade 3 Pancreatic Intraepithelial Neoplasia", "Grade III Pancreatic Intraepithelial Neoplasia", "High Grade Pancreatic Intraepithelial Neoplasia", "High-Grade Pancreatic Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Pancreatic Intraepithelial Neoplasia", "shortest_name_length": 7}
{"curie": "MONDO:0009181", "names": ["MDEBS", "EBSMD", "EBS5B", "EBS-MD", "MD-EBS", "EBS with muscular dystrophy", "Epidermolysa bullosa simplex with muscular dystrophy", "EPIDERMOLYSIS BULLOSA SIMPLEX WITH MUSCULAR DYSTROPHY", "Epidermolysis Bullosa Simplex with Muscular Dystrophy", "Epidermolysis bullosa simplex with muscular dystrophy", "epidermolysis bullosa simplex with muscular dystrophy", "EPIDERMOLYSIS BULLOSA SIMPLEX 5B, WITH MUSCULAR DYSTROPHY", "epidermolysis bullosa simplex 5B, with muscular dystrophy", "epidermolysis bullosa simplex - limb girdle muscular dystrophy", "Epidermolysa bullosa simplex and limb girdle muscular dystrophy", "Epidermolysis bullosa simplex with muscular dystrophy (disorder)", "EPIDERMOLYSIS BULLOSA SIMPLEX AND LIMB-GIRDLE MUSCULAR DYSTROPHY", "Epidermolysis Bullosa Simplex and Limb-Girdle Muscular Dystrophy", "epidermolysis bullosa simplex and limb-girdle muscular dystrophy", "limb-girdle muscular dystrophy with epidermolysis bullosa simplex", "Limb-girdle muscular dystrophy with epidermolysis bullosa simplex", "Limb girdle muscular dystrophy with epidermolysis bullosa simplex"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolysis bullosa simplex 5B, with muscular dystrophy", "shortest_name_length": 5}
{"curie": "MONDO:0001045", "names": ["Bowel atresia", "bowel; atresia", "atresia; bowel", "intestine atresia", "atresia intestine", "Intestinal atresia", "Intestinal Atresia", "intestinal atresia", "Apple Peel Syndrome", "Apple peel syndrome", "Atresia, Intestinal", "Apple Peel Syndromes", "Intestinal atresia NOS", "Atresia of the Intestine", "atresia of the intestine", "Atresia of intestine NOS", "intestinal atresia (disease)", "congenital intestinal atresia", "Apple-Peel Intestinal Atresia", "Congenital Intestinal Atresia", "Congenital intestinal atresia", "Apple Peel Intestinal Atresia", "Intestinal Atresia, Apple-Peel", "Atresia, Congenital Intestinal", "Congenital Intestinal Atresias", "Apple-Peel Intestinal Atresias", "Intestinal Atresia, Congenital", "Atresia, Apple-Peel Intestinal", "Intestinal Atresias, Congenital", "Atresias, Congenital Intestinal", "Atresias, Apple-Peel Intestinal", "Intestinal Atresias, Apple-Peel"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intestinal atresia", "shortest_name_length": 13}
{"curie": "UMLS:C5447319", "names": ["Defects of Intrinsic and Innate Immunity", "Defects in Intrinsic and Innate Immunity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Defects in Intrinsic and Innate Immunity", "shortest_name_length": 40}
{"curie": "MONDO:0014552", "names": ["MKS12", "Meckel syndrome 12", "MECKEL SYNDROME 12", "Meckel syndrome type 12", "lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome", "Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome", "Lethal foetal cerebrorenogenitourinary agenesis/hypoplasia syndrome", "Lethal fetal cerebrorenogenitourinary agenesis or hypoplasia syndrome", "Lethal fetal cerebrorenogenitourinary agenesis or hypoplasia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0034189", "names": ["pyemia", "Pyemia", "PYEMIA", "Pyemias", "Pyaemia", "pyaemia", "Pyohemia", "Pyaemias", "Pyohemias", "Pyemia (disorder)", "pyemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pyemia", "shortest_name_length": 6}
{"curie": "MONDO:0011705", "names": ["LAM", "lymphangiomyomatosis", "LYMPHANGIOMYOMATOSIS", "Pulmonary myomatosis", "Lymphangiomyomatoses", "Lymphangiomyomatosis", "lymphangio-myomatosis", "LYMPHANGIOLEIOMYOMATOSIS", "Lymphangioleiomyomatosis", "Lymphangioleiomyomatoses", "lymphangioleiomyomatosis", "lung lymphangioleiomyomatosis", "PULMONARY LYMPHANGIOMYOMATOSIS", "Pulmonary lymphangiomyomatosis", "lymphangiomyomatosis (diagnosis)", "lymphangioleiomyomatosis, somatic", "pulmonary lymphangioleiomyomatosis", "lymphangioleiomyomatosis (diagnosis)", "Lymphangiomyomatosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphangioleiomyomatosis", "shortest_name_length": 3}
{"curie": "MONDO:0021651", "names": ["SPD", "PPD4", "SDTY2", "synpolydactyly", "Synpolydactyly", "Polysyndactyly", "polysyndactyly", "Synpolydactyly 1", "Syndactyly type 2", "syndactyly type 2", "Syndactyly, type 2", "Syndactyly, Type II", "SYNDACTYLY, TYPE II", "Polysyndactyly syndrome", "Polysyndactyly (disorder)", "Polysyndactyly, unspecified", "Preaxial polydactyly type 4", "Syndactyly type 2 (disorder)", "Syndactyly of multiple digits", "Syndactyly of multiple and unspecified sites"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "synpolydactyly", "shortest_name_length": 3}
{"curie": "UMLS:C0262399", "names": ["SHOULDER BURSITIS", "Shoulder bursitis", "bursitis shoulder", "shoulder bursitis", "Bursitis;shoulder", "bursitis; shoulder", "shoulder; bursitis", "Bursitis of shoulder", "BURSITIS OF SHOULDER", "bursitis of shoulder", "Bursitis of shoulder region", "Bursitis of shoulder (disorder)", "bursitis of shoulder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "shoulder bursitis", "shortest_name_length": 17}
{"curie": "MONDO:0011930", "names": ["ADCME", "FAME2", "BAFME2", "FCMTE2", "familial adult myoclonic epilepsy 2", "Epilepsy, Familial Adult Myoclonic 2", "epilepsy, familial adult myoclonic, 2", "EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2", "epilepsy, familial ADULT myoclonic, 2", "ADRA2B epilepsy, familial adult myoclonic", "epilepsy, familial adult myoclonic, type 2", "benign adult familial myoclonic epilepsy 2", "Benign Adult Familial Myoclonic Epilepsy 2", "BENIGN ADULT FAMILIAL MYOCLONIC EPILEPSY 2", "familial cortical myoclonic tremor and epilepsy 2", "Epilepsy, Myoclonic, Benign Adult Familial, Type 2", "EPILEPSY, MYOCLONIC, BENIGN ADULT FAMILIAL, TYPE 2", "autosomal dominant cortical myoclonus and epilepsy", "CORTICAL MYOCLONUS AND EPILEPSY, AUTOSOMAL DOMINANT", "cortical myoclonus and epilepsy, autosomal dominant", "Cortical Myoclonus And Epilepsy, Autosomal Dominant", "CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 2", "cortical myoclonic tremor with epilepsy, familial, 2", "epilepsy, familial adult myoclonic caused by mutation in ADRA2B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, familial adult myoclonic, 2", "shortest_name_length": 5}
{"curie": "UMLS:C1333458", "names": ["Low Grade Esophageal Squamous Dysplasia", "Low Grade Esophageal Squamous Intraepithelial Neoplasia", "Esophageal Low Grade Squamous Intraepithelial Neoplasia", "Esophageal squamous intraepithelial neoplasia (dysplasia), low grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Grade Esophageal Squamous Intraepithelial Neoplasia", "shortest_name_length": 39}
{"curie": "UMLS:C4682694", "names": ["Stage 0a Penile Cancer", "stage 0a penile cancer", "stage 0a penile cancer AJCC v8", "Stage 0a Penile Cancer AJCC v8", "Stage 0a Penile Squamous Cell Carcinoma AJCC v8", "stage 0a penile squamous cell carcinoma AJCC v8", "Stage 0a Squamous Cell Carcinoma of the Penis AJCC v8", "stage 0a squamous cell carcinoma of the penis AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0a Penile Cancer AJCC v8", "shortest_name_length": 22}
{"curie": "UMLS:C4527010", "names": ["Stage IIIB Retroperitoneal Sarcoma", "Stage IIIB Retroperitoneal Sarcoma AJCC v8", "Stage IIIB Soft Tissue Retroperitoneal Sarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Retroperitoneal Sarcoma AJCC v8", "shortest_name_length": 34}
{"curie": "UMLS:C3897235", "names": ["Untreated Diffuse Astrocytoma", "untreated childhood diffuse astrocytoma", "Untreated Childhood Diffuse Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Untreated Childhood Diffuse Astrocytoma", "shortest_name_length": 29}
{"curie": "MONDO:0030263", "names": ["HLD21", "HYPOMYELINATING LEUKODYSTROPHY 21", "hypomyelinating leukodystrophy 21", "leukodystrophy, hypomyelinating, 21", "LEUKODYSTROPHY, HYPOMYELINATING, 21"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukodystrophy, hypomyelinating, 21", "shortest_name_length": 5}
{"curie": "MONDO:0001141", "names": ["Cholesterin granuloma", "cholesterin granuloma", "middle ear cholesterol granuloma", "Middle Ear Cholesterol Granuloma", "cholesterol granuloma of middle ear", "cholesterin granuloma of middle ear", "Cholesterol Granuloma of Middle Ear", "Cholesterin granuloma of middle ear", "Cholesterin Granuloma of Middle Ear", "Cholesterol granuloma of middle ear", "Cholesterol Granuloma of the Middle Ear", "Cholesterol granuloma of middle ear (disorder)", "cholesterol granuloma of middle ear (diagnosis)", "cholesterin granuloma of middle ear (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "middle ear cholesterol granuloma", "shortest_name_length": 21}
{"curie": "MONDO:0005260", "names": ["ASD", "AUTS1", "autism", "Autism", "childhood autism", "autism (disease)", "infantile autism", "Kanner's syndrome", "Autistic Disorder", "autistic behavior", "Autistic behavior", "autistic disorder", "Autistic behaviors", "Autistic behaviour", "Autistic behaviours", "autism, susceptiblity to", "AUTISM SPECTRUM DISORDER", "autism spectrum disorder", "Autism spectrum disorder", "Autism Spectrum Disorder", "Autism spectrum disorders", "Autism Spectrum Disorders", "Autistic spectrum disorder", "Autistic Spectrum Disorder", "Autistic Spectrum Disorders", "Disorder, Autistic Spectrum", "AUTISM, SUSCEPTIBILITY TO, 1", "Pervasive developmental disorder", "autistic disorder of childhood onset", "autism spectrum disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autism", "shortest_name_length": 3}
{"curie": "MONDO:0021777", "names": ["Acute rheumatic carditis", "acute rheumatic carditis", "Rheumatic carditis, acute", "Acute rheumatic heart disease", "rheumatic heart disease acute", "acute rheumatic heart disease", "acute Rheumatic Heart Disease", "Acute Rheumatic Heart Disease", "Rheumatic heart disease, acute", "Acute rheumatic heart disease, NOS", "Acute rheumatic fever with heart disease", "Rheumatic heart disease, active or acute", "acute rheumatic heart disease (diagnosis)", "heart; disease, rheumatic, active or acute", "Acute rheumatic heart disease, unspecified", "Acute rheumatic fever with heart involvement", "acute rheumatic fever with heart involvement", "active rheumatic fever with heart involvement", "Active rheumatic fever with heart involvement", "rheumatic fever; active with heart involvement", "active; rheumatic fever, with heart involvement", "Acute rheumatic fever with heart disease (disorder)", "Acute Rheumatic fever with unspecified type of heart involvement", "Acute rheumatic fever with unspecified type of heart involvement", "Active rheumatic fever with unspecified type of heart involvement", "Active Rheumatic fever with unspecified type of heart involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute rheumatic heart disease", "shortest_name_length": 24}
{"curie": "UMLS:C3897071", "names": ["Breast Cancer", "Childhood Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Breast Carcinoma", "shortest_name_length": 13}
{"curie": "MONDO:0021477", "names": ["Benign Sphenoid Sinus Tumor", "benign sphenoid sinus tumor", "Benign Sphenoidal Sinus Tumor", "benign sphenoidal sinus tumor", "Benign tumor of sphenoid sinus", "Benign Tumor of Sphenoid Sinus", "benign tumor of sphenoid sinus", "Benign Sphenoid Sinus Neoplasm", "benign sphenoid sinus neoplasm", "Benign tumour of sphenoid sinus", "benign sphenoidal sinus neoplasm", "Benign Tumor of Sphenoidal Sinus", "benign tumor of sphenoidal sinus", "sphenoidal sinus benign neoplasm", "Benign Sphenoidal Sinus Neoplasm", "benign neoplasm of sphenoid sinus", "Benign Neoplasm of Sphenoid Sinus", "Benign Tumor of the Sphenoid Sinus", "benign tumor of the sphenoid sinus", "Benign Neoplasm of Sphenoidal Sinus", "benign neoplasm of sphenoidal sinus", "Benign neoplasm of sphenoidal sinus", "benign tumor of the sphenoidal sinus", "Benign Tumor of the Sphenoidal Sinus", "Benign Neoplasm of the Sphenoid Sinus", "benign neoplasm of the sphenoid sinus", "Benign Neoplasm of the Sphenoidal Sinus", "benign neoplasm of the sphenoidal sinus", "benign neoplasm of sphenoid sinus (diagnosis)", "Benign neoplasm of sphenoidal sinus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of sphenoidal sinus", "shortest_name_length": 27}
{"curie": "MONDO:0020117", "names": ["alpha granule disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alpha granule disease", "shortest_name_length": 21}
{"curie": "MONDO:0010664", "names": ["SRS", "MRXSSR", "Snyder Robinson syndrome", "Snyder-Robinson Syndrome", "Snyder-Robinson syndrome", "spermine synthase deficiency", "Snyder-Robinson syndrome (SRS)", "Snyder-Robinson Mental Retardation Syndrome", "Snyder-Robinson mental retardation syndrome", "SNYDER-ROBINSON MENTAL RETARDATION SYNDROME", "X-linked intellectual disability Snyder type", "X-linked intellectual disability, Snyder type", "Snyder-Robinson intellectual disability syndrome", "X-linked mental retardation Snyder-Robinson type", "X-linked mental retardation Snyder - Robinson type", "Mental Retardation, X-Linked, Snyder-Robinson Type", "mental retardation, X-linked, Snyder-Robinson type", "Mental retardation, x-linked, Snyder-Robinson type", "Snyder-Robinson x-linked mental retardation syndrome", "X-linked intellectual disability Snyder-Robinson type", "syndromic X-linked intellectual disability Snyder type", "X-linked intellectual disability Snyder type (disorder)", "intellectual disability, X-linked, Snyder-Robinson type", "X-linked intellectual disability, Snyder type (diagnosis)", "MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE", "mental retardation, X-linked, syndromic, Snyder-Robinson type", "intellectual disability, X-linked, syndromic, Snyder-Robinson type", "X-linked mental retardation-thin habitus-osteoporosis-kyphoscoliosis syndrome", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE", "intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic X-linked intellectual disability Snyder type", "shortest_name_length": 3}
{"curie": "UMLS:C4682433", "names": ["Stage IIA Vaginal Cancer", "Stage IIA Vaginal Cancer AJCC v8", "Stage IIA Vaginal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Vaginal Cancer AJCC v8", "shortest_name_length": 24}
{"curie": "MONDO:0005219", "names": ["Bloodgood", "breast cystic", "Schimmelbusch", "cystic breast", "Cystic breast", "cystic; breast", "breast; cystic", "breasts cystic", "disease; Cooper", "Cooper; disease", "Cystic Mastitis", "MASTITIS CYSTIC", "Dysplasia;breast", "Breast Dysplasia", "breast dysplasia", "cystic; mastitis", "Breast dysplasia", "mastitis; cystic", "dysplasia mammary", "mammary dysplasia", "breast; dysplasia", "Dysplasia, Breast", "Mammary Dysplasia", "BLOODGOOD DISEASE", "cystic; mastopathy", "Breast fibrocystic", "Dysplasia, Mammary", "mastopathy; cystic", "FIBROCYSTIC BREAST", "Fibrocystic Breast", "fibrocystic breast", "dysplasia; mammary", "BREAST FIBROCYSTIC", "breast fibrocystic", "Fibrocystic breast", "breasts fibrocystic", "Fibrocystic Disease", "fibrocystic breasts", "fibrocystic disease", "Fibrocystic mastitis", "fibrocystic mastitis", "benign breast disease", "breast disease benign", "DISEASE CYSTIC BREAST", "BREAST DISEASE BENIGN", "cystic breast disease", "Disease cystic breast", "SCHIMMELBUSCH DISEASE", "Breast Cystic Disease", "Cystic Breast Disease", "BREAST DISEASE CYSTIC", "Breast cystic fibrosis", "Breast Disease, Cystic", "mastopathy fibrocystic", "Disease, Cystic Breast", "BREAST, CYSTIC DISEASE", "breast cystic fibrosis", "fibrocystic mastopathy", "Fibrocystic mastopathy", "Fibrocystic Mastopathy", "benign breast diseases", "Breast Cystic Diseases", "BREAST CYSTIC FIBROSIS", "chronic cystic mastitis", "Schimmelbusch's disease", "Mastopathy, Fibrocystic", "Chronic cystic mastitis", "Chronic Cystic Mastitis", "Cystic disease of breast", "Cystic Mastitis, Chronic", "Cystic Disease of Breast", "MASTITIS, CHRONIC CYSTIC", "cystic disease of breast", "diffuse cystic mastopathy", "breast Fibrocystic Change", "Diffuse cystic mastopathy", "Breast fibrocystic change", "BREAST FIBROCYSTIC CHANGE", "breast fibrocystic change", "Breast Fibrocystic Change", "Diffuse Cystic Mastopathy", "fibrocystic breast change", "Fibrocystic Breast Disease", "Fibrocystic breast disease", "Breast Fibrocystic Disease", "breast fibrocystic changes", "DISEASE FIBROCYSTIC BREAST", "mastopathy; diffuse cystic", "Fibrocystic breast changes", "hyperplasia; Schimmelbusch", "BREAST DISEASE FIBROCYSTIC", "fibrocystic breast disease", "diffuse; cystic mastopathy", "fibrocystic breast changes", "FIBROCYSTIC BREAST DISEASE", "Disease fibrocystic breast", "breast disease fibrocystic", "Fibrocystic disease breast", "Schimmelbusch; hyperplasia", "Breast Fibrocystic Changes", "breast fibrocystic disease", "BREAST FIBROCYSTIC DISORDER", "Breast--Fibrocystic disease", "Breast Disease, Fibrocystic", "BREAST, FIBROCYSTIC DISEASE", "breasts disease fibrocystic", "Disease, Fibrocystic Breast", "Fibrocystic disease, breast", "Breast fibrocystic disorder", "breasts changes fibrocystic", "disease; fibrocystic, breast", "Cystic Disease of the Breast", "Fibrocystic Change of Breast", "fibrocystic change of breast", "fibrocystic; disease, breast", "cystic disease of the breast", "Fibrocystic change of breast", "breast; disorder, fibrocystic", "Fibrocystic Disease of Breast", "fibrocystic changes in breast", "of fibrocystic breast disease", "Fibrocystic disease of breast", "Fibrocystic Changes of Breast", "Chronic cystic disease breast", "fibrocystic disease of breast", "FIBROCYSTIC DISEASE OF BREAST", "Gross cystic disease of breast", "fibrocystic change of the breast", "FBD (fibrocystic breast disease)", "Fibrocystic Change of the Breast", "Fibrocystic Disease of the Breast", "fibrocystic disease of the breast", "cystic; disease, breast (chronic)", "breast; disorder, cystic (chronic)", "chronic cystic mastitis (diagnosis)", "Fibrocystic breast changes (finding)", "fibrocystic disease of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast fibrocystic disease", "shortest_name_length": 9}
{"curie": "MONDO:0016953", "names": ["Trisomy 2q", "trisomy 2q", "2q trisomy", "2q+ syndrome", "2q duplication", "Duplication 2q", "dup(2q) syndrome", "partial trisomy 2q", "duplication 2q syndrome", "2q duplication syndrome", "Chromosome 2, trisomy 2q", "chromosome 2q duplication", "chromosome 2q trisomy syndrome", "partial trisomy of chromosome 2q", "chromosome 2q duplication syndrome", "partial duplication of chromosome 2q", "partial trisomy of the long arm of chromosome 2", "partial duplication of the long arm of chromosome 2", "partial duplication of the long arm of chromosome type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of the long arm of chromosome 2", "shortest_name_length": 10}
{"curie": "UMLS:C0032966", "names": ["Neoplastic Pregnancy Complication", "Neoplastic Pregnancy Complications", "Complication, Neoplastic Pregnancy", "Pregnancy Complication, Neoplastic", "Pregnancy Complications, Neoplastic", "Complications, Neoplastic Pregnancy", "Pregnancy, Neoplastic Complications", "Pregnancies, Neoplastic Complications"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pregnancy Complications, Neoplastic", "shortest_name_length": 33}
{"curie": "UMLS:C0686617", "names": ["Metastasis to thymus", "Metastasis to the Thymus", "Metastatic Tumor to the Thymus", "Metastatic Neoplasm to the Thymus", "thymus neoplasm malignant secondary", "Secondary malignant tumor of thymus", "Secondary malignant tumour of thymus", "Secondary malignant neoplasm of thymus", "Secondary Malignant Tumor to the Thymus", "Metastatic malignant neoplasm to thymus", "Metastatic malignant neoplasm of thymus", "Metastatic Malignant Tumor to the Thymus", "Secondary Malignant Neoplasm to the Thymus", "Metastatic Malignant Neoplasm to the Thymus", "Metastatic Malignant Neoplasm in the Thymus", "Metastatic malignant neoplasm to thymus (disorder)", "Secondary malignant neoplasm of thymus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to thymus", "shortest_name_length": 20}
{"curie": "MONDO:0016796", "names": ["mtDNA depletion syndrome, encephalomyopathic form", "mitochondrial DNA depletion syndrome, encephalomyopathic form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial DNA depletion syndrome, encephalomyopathic form", "shortest_name_length": 49}
{"curie": "MONDO:0008221", "names": ["Iminodipeptiduria", "Peptidase deficiency", "PROLIDASE DEFICIENCY", "prolidase deficiency", "Prolidase Deficiency", "peptidase deficiency", "Prolidase deficiency", "Deficiency, Prolidase", "hyperimidodipeptiduria", "Hyperimidodipeptiduria", "Prolidase Deficiencies", "Deficiencies, Prolidase", "Deficiency of prolidase", "Hyperimidodipeptidurias", "imidodipeptidase deficiency", "Imidodipeptidase Deficiency", "Imidodipeptidase deficiency", "Deficiency, Imidodipeptidase", "Imidodipeptidase Deficiencies", "Deficiency of imidodipeptidase", "Proline dipeptidase deficiency", "Deficiencies, Imidodipeptidase", "Deficiency of proline dipeptidase", "Deficiency of prolidase (disorder)", "Deficiency of imidodipeptidase (disorder)", "Deficiency of proline dipeptidase (disorder)", "Prolidase deficiency with hyperimidodipeptiduria", "Hyperimidodipeptiduria due to proline dipeptidase deficiency", "Hyperimidodipeptiduria due to proline dipeptidase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prolidase deficiency", "shortest_name_length": 17}
{"curie": "UMLS:C4553870", "names": ["IVB", "stage IVB bladder cancer", "Stage IVB Bladder Cancer", "Stage IVB Bladder Cancer AJCC v8", "stage IVB bladder cancer AJCC v8", "Stage IVB Bladder Carcinoma AJCC v8", "stage IVB bladder carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Bladder Cancer AJCC v8", "shortest_name_length": 3}
{"curie": "MONDO:0006000", "names": ["tb peritonitis", "peritonitis tb", "peritonitis, tb", "peritoneum tuberculosis", "PERITONITIS TUBERCULOUS", "tuberculous peritonitis", "peritonitis tuberculous", "peritoneal tuberculosis", "tuberculosis peritoneal", "Peritoneal tuberculosis", "TUBERCULOUS PERITONITIS", "Tuberculous peritonitis", "Peritonitis, Tuberculous", "Tuberculosis, Peritoneal", "Peritonitis - tuberculous", "tuberculosis of peritoneum", "Tuberculosis of peritoneum", "Tuberculosis (TB) peritonitis", "Tuberculous peritonitis (disorder)", "peritoneum; tuberculous (etiology)", "peritonitis; tuberculous (etiology)", "tuberculosis; peritoneum (etiology)", "tuberculous peritonitis (diagnosis)", "Mycobacterium tuberculosis peritonitis", "tuberculosis of peritoneum (diagnosis)", "peritoneum; tuberculous (manifestation)", "tuberculosis; peritoneum (manifestation)", "peritonitis; tuberculous (manifestation)", "Mycobacterium tuberculosis caused peritonitis", "peritoneum; tuberculous peritonitis (etiology)", "peritoneum; tuberculous peritonitis (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tuberculous peritonitis", "shortest_name_length": 14}
{"curie": "UMLS:C4727357", "names": ["Recurrent Acinic Cell Breast Carcinoma", "Recurrent Breast Acinic Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Breast Acinic Cell Carcinoma", "shortest_name_length": 38}
{"curie": "UMLS:C2983718", "names": ["Prostate Cancer by AJCC v6 Stage", "Prostate Carcinoma by AJCC v6 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Cancer by AJCC v6 Stage", "shortest_name_length": 32}
{"curie": "MONDO:0022060", "names": ["calloso-genital dysplasia", "Calloso-genital dysplasia", "Primary amenorrhoea with coloboma and total agenesis of the corpus callosum", "primary amenorrhoea with coloboma and total agenesis of the corpus callosum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "calloso-genital dysplasia", "shortest_name_length": 25}
{"curie": "UMLS:C0333894", "names": ["Post-Radiation Cytologic Changes with Dysplasia", "Post-radiation cytologic changes with dysplasia", "Post-radiation cytologic changes with dysplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post-radiation cytologic changes with dysplasia", "shortest_name_length": 47}
{"curie": "MONDO:0030920", "names": ["MRD54", "autosomal dominant mental retardation 54", "mental retardation, autosomal dominant 54", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 54", "autosomal dominant intellectual disability 54", "intellectual disability, autosomal dominant 54", "autosomal dominant intellectual developmental disorder 54", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 54"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 54", "shortest_name_length": 5}
{"curie": "MONDO:0017108", "names": ["isolated total cerebellar vermis agenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated total cerebellar vermis agenesis", "shortest_name_length": 41}
{"curie": "MONDO:0007363", "names": ["DA9", "CCA", "CCA syndrome", "Beals syndrome", "Beals Syndrome", "BEALS SYNDROME", "Beal's syndrome", "Beals-Hecht syndrome", "distal arthrogryposis type 9", "Distal arthrogryposis type 9", "arthrogryposis distal type 9", "ARTHROGRYPOSIS, DISTAL, TYPE 9", "Arthrogryposis, Distal, Type 9", "arthrogryposis, distal, type 9", "Congenital Contractural Arachnodactyly", "Congenital contractural arachnodactyly", "congenital contractural arachnodactyly", "arachnodactyly, contractural Beals type", "CONTRACTURAL ARACHNODACTYLY, CONGENITAL", "Arachnodactyly, contractural Beals type", "contractural arachnodactyly, congenital", "Contractural Arachnodactyly, Congenital", "arthrogryposis distal type 9 (diagnosis)", "contractures, multiple with arachnodactyly", "Contractures, multiple with arachnodactyly", "CCA - Congenital contractural arachnodactyly", "Congenital contractural arachnodactyly (disorder)", "Ear anomalies-contractures-dysplasia of bone with kyphoscoliosis", "ear anomalies-contractures-dysplasia of bone with kyphoscoliosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital contractural arachnodactyly", "shortest_name_length": 3}
{"curie": "MONDO:0000631", "names": ["benign tumor bone", "Benign Bone Tumor", "BONE TUMOR BENIGN", "Bone tumor benign", "Benign bone tumor", "benign bone tumor", "benign bone tumors", "Benign bone tumour", "Bone tumour benign", "benign bone tumours", "benign osseous tumor", "benign tumor of bone", "Benign Osseous Tumor", "bone benign neoplasm", "benign bone neoplasm", "Benign bone neoplasm", "Benign Tumor of Bone", "Benign Bone Neoplasm", "benign osseous neoplasm", "benign neoplasm of bone", "Neoplasm benign;bone(s)", "Benign Osseous Neoplasm", "Benign Neoplasm of Bone", "Benign neoplasm of bone", "Benign Tumor of the Bone", "benign tumor of the bone", "Benign bone neoplasm NOS", "bone neoplasm, benign, NOS", "bone tissue benign neoplasm", "benign neoplasm of the bone", "Benign Neoplasm of the Bone", "Benign neoplasm of bone, NOS", "benign neoplasm of the bone(s)", "Benign neoplasm of bone (disorder)", "benign neoplasm of bone (diagnosis)", "Benign osseous and chondromatous tumor", "Benign osseous and chondromatous tumour", "Benign tumor of bone and articular cartilage", "Benign tumour of bone and articular cartilage", "Benign neoplasm of bone and articular cartilage", "Benign neoplasm of bone and articular cartilage, NOS", "Benign neoplasm of bone and articular cartilage, unspecified", "Benign neoplasm of bone and articular cartilage, site unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bone benign neoplasm", "shortest_name_length": 17}
{"curie": "UMLS:C5206377", "names": ["Refractory Rectal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Rectal Adenocarcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C0011052", "names": ["Prelingual Deafness", "Deafness, Prelingual"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prelingual Deafness", "shortest_name_length": 19}
{"curie": "MONDO:0009321", "names": ["Kleiner-Holmes syndrome", "Kleiner Holmes syndrome", "Hallux varus and preaxial polysyndactyly", "HALLUX VARUS AND PREAXIAL POLYSYNDACTYLY", "hallux varus and preaxial polysyndactyly", "hallux varus-preaxial polysyndactyly syndrome", "Hallux varus-preaxial polysyndactyly syndrome", "Hallux varus, preaxial polysyndactyly syndrome", "Hallux varus, preaxial polysyndactyly syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hallux varus-preaxial polysyndactyly syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0012596", "names": ["PSATD", "PSAT Deficiency", "PSAT deficiency", "PSAT DEFICIENCY", "PSAT deficiency, infantile/juvenile form", "Phosphoserine aminotransferase deficiency", "phosphoserine aminotransferase deficiency", "PHOSPHOSERINE AMINOTRANSFERASE DEFICIENCY", "Phosphoserine Aminotransferase Deficiency", "Deficiency of phosphoserine aminotransferase", "Deficiency of phosphoserine aminotransferase (disorder)", "Phosphoserine aminotransferase deficiency, infantile/juvenile form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PSAT deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C4763762", "names": ["Metastatic Adenoid Cystic Cancer", "Adenoid cystic carcinoma metastatic", "Metastatic Adenoid Cystic Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenoid cystic carcinoma metastatic", "shortest_name_length": 32}
{"curie": "UMLS:C5238836", "names": ["Pathologic Murmur", "Pathologic murmur"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Murmur", "shortest_name_length": 17}
{"curie": "MONDO:0003897", "names": ["Epithelioid Breast Hemangioma", "Breast Epithelioid Hemangioma", "breast epithelioid hemangioma", "epithelioid breast hemangioma", "Breast Histiocytoid Hemangioma", "histiocytoid breast hemangioma", "breast histiocytoid hemangioma", "breast Histiocytoid hemangioma", "Histiocytoid Breast Hemangioma", "Epithelioid Hemangioma of Breast", "epithelioid hemangioma of breast", "Histiocytoid Hemangioma of Breast", "histiocytoid hemangioma of breast", "Epithelioid Hemangioma of the Breast", "epithelioid hemangioma of the breast", "histiocytoid hemangioma of the breast", "Histiocytoid Hemangioma of the Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast epithelioid hemangioma", "shortest_name_length": 29}
{"curie": "MONDO:0000474", "names": ["pericardial disease", "Disease;pericardium", "PERICARDIAL DISEASE", "Pericardial disease", "pericardium disease", "diseases pericardium", "pericardial diseases", "PERICARDIAL DISEASES", "pericardium disorder", "Pericardial disorder", "Pericardial Disorders", "Pericardial disorders", "disease of pericardium", "Pericardial disease NOS", "Disorder of pericardium", "disorder of pericardium", "Pericardial disorder, NOS", "Disease of pericardium, NOS", "pericardium disease or disorder", "pericardial disease (diagnosis)", "Pericardial disease or syndrome", "Disorder of pericardium (disorder)", "disease or disorder of pericardium", "Pericardial Diseases and Syndromes", "Unspecified disease of pericardium", "Disease of pericardium, unspecified", "disorder of pericardium (diagnosis)", "PERICARDIAL DISEASES: GENERAL CONDITIONS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pericardium disorder", "shortest_name_length": 19}
{"curie": "MONDO:0012716", "names": ["Sed-BDS", "SED-BDS", "Tatoo dysplasia", "TATOO DYSPLASIA", "Tattoo Dysplasia", "tattoo dysplasia", "Tattoo dysplasia", "FANTASY ISLAND SYNDROME", "fantasy Island syndrome", "Fantasy Island Syndrome", "Fantasy Island syndrome", "Spondyloepiphyseal dysplasia Cantu type", "SED-brachydactyly and distinctive speech", "spondyloepiphyseal dysplasia, Cantu type", "SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH", "Spondyloepiphyseal Dysplasia-Brachydactyly and Distinctive Speech", "spondyloepiphyseal dysplasia-brachydactyly and distinctive speech", "spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome", "Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome", "Spondyloepiphyseal dysplasia and brachydactyly with speech disorder syndrome", "Spondyloepiphyseal dysplasia and brachydactyly with speech disorder syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepiphyseal dysplasia, Cantu type", "shortest_name_length": 7}
{"curie": "MONDO:0013766", "names": ["FACU", "plaid", "FCAS3", "PLAID", "FAMILIAL ATYPICAL COLD URTICARIA", "Familial atypical cold urticaria", "familial atypical cold urticaria", "FACU - familial atypical cold urticaria", "FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 3", "familial cold autoinflammatory syndrome 3", "PLCG2 familial cold autoinflammatory syndrome", "familial cold autoinflammatory syndrome type 3", "Familial cold urticaria with common variable immunodeficiency", "familial cold urticaria with common variable immunodeficiency", "PLCG2-associated antibody deficiency and immune dysregulation", "ANTIBODY DEFICIENCY AND IMMUNE DYSREGULATION, PLCG2-ASSOCIATED", "antibody deficiency and immune dysregulation, PLCG2-associated", "familial cold autoinflammatory syndrome caused by mutation in PLCG2", "Phospholipase C gamma 2 associated antibody deficiency and immune dysregulation", "PLCG2 (phospholipase C gamma 2) associated antibody deficiency and immune dysregulation", "Phospholipase C gamma 2 associated antibody deficiency and immune dysregulation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial cold autoinflammatory syndrome 3", "shortest_name_length": 4}
{"curie": "MONDO:0037735", "names": ["sebaceous gland cancer", "cancer of sebaceous gland", "malignant sebaceous tumor", "Malignant Sebaceous Tumor", "malignant sebaceous neoplasm", "Malignant Sebaceous Neoplasm", "malignant sebaceous gland tumor", "Malignant Sebaceous Gland Tumor", "Malignant Tumor of Sebaceous Gland", "malignant sebaceous gland neoplasm", "malignant tumor of sebaceous gland", "Malignant Sebaceous Gland Neoplasm", "Malignant Neoplasm of Sebaceous Gland", "malignant neoplasm of sebaceous gland", "Malignant neoplasm of sebaceous gland", "malignant neoplasm of sebaceous glands", "malignant tumor of the sebaceous gland", "Malignant Tumor of the Sebaceous Gland", "Malignant Neoplasm of the Sebaceous Gland", "malignant neoplasm of the sebaceous gland", "malignant neoplasm of sebaceous gland (diagnosis)", "neoplasm of integumentary system sebaceous gland malignant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sebaceous gland cancer", "shortest_name_length": 22}
{"curie": "UMLS:C4552684", "names": ["Stage I", "Stage I Uterine Corpus Cancer AJCC v8", "Stage I Uterine (including Endometrial) Cancer", "Stage I Uterine Corpus Carcinoma or Carcinosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Uterine Corpus Cancer AJCC v8", "shortest_name_length": 7}
{"curie": "UMLS:C4054914", "names": ["Fusion-Negative Alveolar Rhabdomyosarcoma", "Fusion Gene Negative Alveolar Rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fusion-Negative Alveolar Rhabdomyosarcoma", "shortest_name_length": 41}
{"curie": "UMLS:C0234462", "names": ["Ageusic Aphasia", "Ageusic aphasia", "Ageusic Aphasias", "Aphasia, Ageusic", "Aphasia, ageusic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aphasia, Ageusic", "shortest_name_length": 15}
{"curie": "MONDO:0005002", "names": ["COPD", "cold", "COAD", "coad", "COLD", "copd", "COPD NOS", "chronic airway disease", "Chronic airway disease", "chronic airways disease", "Chronic airways disease", "Obstructive Lung Disease", "COPD, SEVERE EARLY-ONSET", "COPD, Severe Early-Onset", "Chronic airflow limitation", "chronic airflow limitation", "chronic obstr lung disease", "Chronic airway obstruction", "Chronic obstr lung disease", "Hyperactive airway disease", "HYPERACTIVE AIRWAY DISEASE", "AIRWAY OBSTRUCTION CHRONIC", "Chronic airflow obstruction", "Chronic Airflow Obstruction", "Chronic obstr pulmon disease", "obstruction; airway, chronic", "Airflow Obstruction, Chronic", "chronic obstr pulmon disease", "Chronic Airflow Obstructions", "airway; obstruction, chronic", "Airflow Obstructions, Chronic", "Chronic obstr airways disease", "Chronic pulmonary obstruction", "chronic obstr airways disease", "Chronic obstructive lung disease", "chronic obstructive lung disease", "Chronic Obstructive Lung Disease", "CAL - Chronic airflow limitation", "CHRONIC OBSTRUCT AIRWAYS DISEASE", "Chronic obstruct airways disease", "CHRONIC OBSTRUCTIVE LUNG DISEASE", "CAFL - Chronic airflow limitation", "obstructive lung disease, chronic", "CAO - Chronic airflow obstruction", "Chronic Obstructive Airway Disease", "Chronic obstructive airway disease", "chronic obstructive airway disease", "lung; obstruction, disease, chronic", "obstruction; lung, disease, chronic", "Chronic Obstructive Airways Disease", "chronic obstructive airways disease", "disease (COPD), chronic obstructive", "Chronic obstructive airways disease", "Chronic obstructive lung disease NOS", "lung; disease, obstructive (chronic)", "Chronic Obstructive Pulmonary Disease", "CHRONIC OBSTRUCTIVE PULMONARY DISEASE", "Chronic obstructive pulmonary disease", "Chronic obstructive lung disease, NOS", "chronic obstructive pulmonary disease", "Obstructive airways disease (chronic)", "Chronic obstructive bronchopneumopathy", "PULMONARY DISEASE, CHRONIC OBSTRUCTIVE", "Chronic Obstructive Pulmonary Diseases", "Chronic obstructive airway disease NOS", "Pulmonary Disease, Chronic Obstructive", "cold (chronic obstructive lung disease)", "COLD - Chronic obstructive lung disease", "Chronic irreversible airway obstruction", "COLD (chronic obstructive lung disease)", "Chronic obstructive pulmonary disease NOS", "COAD - Chronic obstructive airways disease", "Chronic obstructive lung disease (disorder)", "COPD, chronic obstructive pulmonary disease", "chronic obstructive pulmonary disease (COPD)", "COPD - Chronic obstructive pulmonary disease", "Chronic obstructive pulmonary disease (COPD)", "Chronic Obstructive Pulmonary Disease (COPD)", "pulmonary disease (COPD), chronic obstructive", "obstructive pulmonary disease (COPD), chronic", "chronic obstructive pulmonary disease, (COPD)", "respiratory tract; disorder, chronic, obstructive", "chronic obstructive pulmonary disease (diagnosis)", "respiratory tract; disorder, obstructive, chronic", "Chronic obstructive pulmonary disease, unspecified", "Chronic airway obstruction; not otherwise specified", "Pulmonary Disease, Chronic Obstructive, Severe Early-Onset", "PULMONARY DISEASE, CHRONIC OBSTRUCTIVE, SEVERE EARLY-ONSET", "disease (or disorder); respiratory tract, obstructive, chronic", "disease (or disorder); respiratory tract, chronic, obstructive", "PULMONARY DISEASE, CHRONIC OBSTRUCTIVE, RATE OF DECLINE OF LUNG FUNCTION IN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic obstructive pulmonary disease", "shortest_name_length": 4}
{"curie": "MONDO:0017744", "names": ["disorder of O-xylosyl/N-acetylgalactosaminylglycan synthesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of O-xylosyl/N-acetylgalactosaminylglycan synthesis", "shortest_name_length": 60}
{"curie": "MONDO:0004578", "names": ["Flat retinoschisis", "flat retinoschisis", "Flat retinoschisis (disorder)", "flat retinoschisis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "flat retinoschisis", "shortest_name_length": 18}
{"curie": "MONDO:0015036", "names": ["Lissencephaly with cerebellar hypoplasia type C", "lissencephaly with cerebellar hypoplasia type C", "Lissencephaly co-occurrent with congenital cerebellar hypoplasia type C", "Lissencephaly co-occurrent with congenital cerebellar hypoplasia type C (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lissencephaly with cerebellar hypoplasia type C", "shortest_name_length": 47}
{"curie": "UMLS:C4526905", "names": ["Stage IIIA Soft Tissue Sarcoma of the Trunk and Extremities", "Stage IIIA Soft Tissue Sarcoma of the Trunk and Extremities AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Soft Tissue Sarcoma of the Trunk and Extremities AJCC v8", "shortest_name_length": 59}
{"curie": "MONDO:0005821", "names": ["Juvenile syphilis", "juvenile syphilis", "Juvenile neurosyphilis", "juvenile neurosyphilis", "Neurosyphilis, Juvenile", "juvenile; neurosyphilis", "neurosyphilis; juvenile", "late congenital syphilis", "Late congenital syphilis", "Juvenile neurosyphilis NOS", "SYPHILIS, CONGENITAL, LATE", "Late congenital neurosyphilis", "Juvenile neurosyphilis, unspecified", "late congenital syphilis (diagnosis)", "late symptomatic congenital syphilis", "Late congenital syphilis, unspecified", "Late congenital neurosyphilis (disorder)", "Other symptomatic late congenital syphilis", "Late congenital syphilis (2 years OR more)", "late congenital syphilis (2 years or more)", "Other late congenital syphilis, symptomatic", "Late congenital syphilis, NOS (2 years or more)", "late symptomatic congenital syphilis (diagnosis)", "Late congenital syphilis (2 years OR more) (disorder)", "Late congenital neurosyphilis [juvenile neurosyphilis]", "Congenital syphilis NOS, two years or more after birth", "Congenital syphilis NOS two years or more after birth.", "Late congenital syphilis, symptomatic (2 years OR more)", "Late congenital syphilis, symptomatic (2 years or more)", "late congenital syphilis, symptomatic (2 years or more)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "late congenital syphilis", "shortest_name_length": 17}
{"curie": "MONDO:0016362", "names": ["AAPC", "AFAP", "HFAS", "attenuated FAP", "Attenuated FAP", "mild form of FAP", "Hereditary Flat Adenoma Syndrome", "hereditary flat adenoma syndrome", "Attenuated familial polyposis coli", "attenuated familial polyposis coli", "attenuated adenomatous polyposis coli", "Attenuated Adenomatous Polyposis Coli", "ADENOMATOUS POLYPOSIS COLI, ATTENUATED", "Attenuated Familial Adenomatous Polyposis", "attenuated familial adenomatous polyposis", "Attenuated familial adenomatous polyposis", "Familial Adenomatous Polyposis, Attenuated", "FAMILIAL ADENOMATOUS POLYPOSIS, ATTENUATED", "Attenuated familial adenomatous polyposis (disorder)", "FAMILIAL ADENOMATOUS POLYPOSIS, ATTENUATED (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "attenuated familial adenomatous polyposis", "shortest_name_length": 4}
{"curie": "UMLS:C0434133", "names": ["bladder perforation", "Bladder perforation", "Bladder Perforation", "Perforation of bladder", "perforation of bladder", "Perforation of bladder (disorder)", "perforation of bladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perforation of bladder", "shortest_name_length": 19}
{"curie": "MONDO:0004044", "names": ["Ureter Urothelial Papilloma", "ureter urothelial papilloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ureter urothelial papilloma", "shortest_name_length": 27}
{"curie": "MONDO:0016681", "names": ["Gliosarcoma", "gliosarcoma", "Gliosarcomas", "Sarcomatous Glioma", "Glioma, Sarcomatous", "Sarcomatous Gliomas", "Gliomas, Sarcomatous", "sarcomatous glioblastoma", "gliosarcoma; unspecified site", "Gliosarcoma (morphologic abnormality)", "Glioblastoma with Sarcomatous Component", "Glioblastoma with sarcomatous component", "glioblastoma with sarcomatous component", "Glioblastoma with a Sarcomatous Component", "glioblastoma with a sarcomatous component"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gliosarcoma", "shortest_name_length": 11}
{"curie": "UMLS:C4682563", "names": ["Stage IV Uterine Corpus Leiomyosarcoma", "Stage IV Uterine Corpus Leiomyosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Uterine Corpus Leiomyosarcoma AJCC v8", "shortest_name_length": 38}
{"curie": "UMLS:C1710668", "names": ["Pancreatic NET G2", "Pancreatic Neuroendocrine Tumor G2", "Well Differentiated Pancreatic Endocrine Carcinoma", "Well Differentiated Pancreatic Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Neuroendocrine Tumor G2", "shortest_name_length": 17}
{"curie": "UMLS:C0434514", "names": ["dislocated spine", "Spine dislocation", "dislocation spine", "spine dislocation", "Dislocated vertebra", "vertebra dislocation", "dislocation; vertebra", "Dislocation of vertebra", "dislocation of vertebra", "Dislocation of joint of spine", "dislocation of vertebra (diagnosis)", "Dislocation of joint of spine (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dislocation of joint of spine", "shortest_name_length": 16}
{"curie": "UMLS:C4763546", "names": ["Unresectable Basal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Basal Cell Carcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C3273094", "names": ["Gallbladder Papillary Neoplasm with Intermediate Grade Intraepithelial Neoplasia", "Intracystic papillary neoplasm with intermediate grade intraepithelial neoplasia", "Gallbladder Intracholecystic Papillary (Tubular) Neoplasm with Intermediate Grade Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gallbladder Intracholecystic Papillary (Tubular) Neoplasm with Intermediate Grade Intraepithelial Neoplasia", "shortest_name_length": 80}
{"curie": "MONDO:0001883", "names": ["Blue Toe Syndrome", "blue toe syndrome", "Blue toe syndrome", "Syndrome, Blue Toe"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blue toe syndrome", "shortest_name_length": 17}
{"curie": "UMLS:C4744857", "names": ["Advanced Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Neuroendocrine Neoplasm", "shortest_name_length": 32}
{"curie": "UMLS:C5556721", "names": ["Advanced HER2-Positive Breast Carcinoma", "Advanced HER2 Positive Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced HER2-Positive Breast Carcinoma", "shortest_name_length": 39}
{"curie": "UMLS:C0333877", "names": ["Mild columnar cell atypia", "Mild Columnar Cell Atypia", "Mild columnar cell atypia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mild columnar cell atypia", "shortest_name_length": 25}
{"curie": "MONDO:0012232", "names": ["STUT2", "Stuttering, Familial Persistent 2", "STUTTERING, FAMILIAL PERSISTENT, 2", "stuttering, familial persistent, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stuttering, familial persistent, 2", "shortest_name_length": 5}
{"curie": "MONDO:0005416", "names": ["Knee osteoarthritis", "osteoarthritis, knee", "Osteoarthritis, Knee"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteoarthritis, knee", "shortest_name_length": 19}
{"curie": "UMLS:C4727741", "names": ["Refractory Female Reproductive System Cancer", "Refractory Female Reproductive System Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Female Reproductive System Carcinoma", "shortest_name_length": 44}
{"curie": "UMLS:C5420647", "names": ["Unresectable Vulvar Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Vulvar Squamous Cell Carcinoma", "shortest_name_length": 43}
{"curie": "UMLS:C1512746", "names": ["Infiltrating Bladder Urothelial Carcinoma with Giant Cells"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infiltrating Bladder Urothelial Carcinoma with Giant Cells", "shortest_name_length": 58}
{"curie": "UMLS:C0273163", "names": ["pancreas injury", "injury; pancreas", "pancreas; injury", "Pancreatic Trauma", "Pancreatic trauma", "pancreatic injury", "Pancreatic Injury", "Pancreatic injury", "injuries pancreas", "trauma pancreatic", "pancreatic trauma", "injury of pancreas", "Injury of pancreas", "Injury of pancreas, NOS", "Injury of pancreas (disorder)", "injury of pancreas (diagnosis)", "injury to gastrointestinal tract pancreas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of pancreas", "shortest_name_length": 15}
{"curie": "UMLS:C2750414", "names": ["Cap Myopathy, Tpm3-Related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cap Myopathy, Tpm3-Related", "shortest_name_length": 26}
{"curie": "UMLS:C1336258", "names": ["Stage III Nodular Lymphocyte Predominant Hodgkin Lymphoma", "Stage III Nodular Lymphocyte Predominant Hodgkin's Disease", "Stage III Nodular Lymphocyte Predominant Hodgkin's Lymphoma", "Ann Arbor Stage III Nodular Lymphocyte Predominant Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage III Nodular Lymphocyte Predominant Hodgkin Lymphoma", "shortest_name_length": 57}
{"curie": "UMLS:C4744369", "names": ["Sellar Meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sellar Meningioma", "shortest_name_length": 17}
{"curie": "MONDO:0023021", "names": ["dwarfism lethal type advanced bone age"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dwarfism lethal type advanced bone age", "shortest_name_length": 38}
{"curie": "MONDO:0040675", "names": ["myofibroblastoma", "Myofibroblastoma", "Myofibroblastomas", "Myofibroblastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myofibroblastoma", "shortest_name_length": 16}
{"curie": "MONDO:0002604", "names": ["Pericytic tumor", "Pericytic Tumor", "Pericytic neoplasm", "pericytic neoplasm", "Pericytic Neoplasm", "perivascular tumor", "Perivascular Tumor", "perivascular neoplasm", "Perivascular Neoplasm", "Malignant Pericytic Tumor", "Malignant Perivascular Tumor", "Malignant Pericytic Neoplasm", "malignant perivascular cancer", "Malignant Perivascular Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pericytic neoplasm", "shortest_name_length": 15}
{"curie": "UMLS:C4721658", "names": ["Stage II Ovarian Teratoma", "Stage II Ovarian Teratoma AJCC v7", "Stage II Ovarian Teratoma AJCC v6", "Stage II Ovarian Germ Cell Teratoma", "Ovarian Germ Cell Teratoma Stage II", "Ovarian Germ Cell Teratoma, Stage II", "Stage II Ovarian Teratoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Ovarian Teratoma AJCC v6 and v7", "shortest_name_length": 25}
{"curie": "MONDO:0010214", "names": ["XPV", "Xeroderma pigmentosum variant", "xeroderma pigmentosum variant", "Xeroderma Pigmentosum Variant Type", "xeroderma pigmentosum variant type", "Xeroderma pigmentosum, variant type", "XERODERMA PIGMENTOSUM, VARIANT TYPE", "xeroderma pigmentosum, variant type", "photosensitivity with defective DNA synthesis", "Photosensitivity with defective DNA synthesis", "PHOTOSENSITIVITY WITH DEFECTIVE DNA SYNTHESIS", "XERODERMA PIGMENTOSUM WITH NORMAL DNA REPAIR RATES", "xeroderma pigmentosum with normal DNA repair rates", "Xeroderma pigmentosum with normal DNA repair rates"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "xeroderma pigmentosum variant type", "shortest_name_length": 3}
{"curie": "MONDO:0005201", "names": ["Cardiomyopathy;restrictive", "Restrictive Cardiomyopathy", "restrictive cardiomyopathy", "Restrictive cardiomyopathy", "cardiomyopathy restrictive", "Cardiomyopathy, restrictive", "Constrictive cardiomyopathy", "restrictive; cardiomyopathy", "cardiomyopathy; restrictive", "CARDIOMYOPATHY, RESTRICTIVE", "constrictive cardiomyopathy", "Cardiomyopathy, Restrictive", "cardiomyopathy, constrictive", "Restrictive Cardiomyopathies", "Cardiomyopathy, constrictive", "Cardiomyopathies, Restrictive", "Constrictive cardiomyopathy NOS", "RCM - Restrictive cardiomyopathy", "primary restrictive cardiomyopathy", "Primary restrictive cardiomyopathy", "Familial Restrictive Cardiomyopathy", "Familial restrictive cardiomyopathy", "familial restrictive cardiomyopathy", "Restrictive cardiomyopathy (disorder)", "restrictive cardiomyopathy (diagnosis)", "constrictive cardiomyopathy (diagnosis)", "Primary restrictive cardiomyopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "restrictive cardiomyopathy", "shortest_name_length": 26}
{"curie": "MONDO:0007727", "names": ["FHF", "FPF", "TRAPS", "TRAPS syndrome", "familial Hibernian fever", "Hibernian Familial Fever", "FAMILIAL HIBERNIAN FEVER", "Familial Hibernian Fever", "Familial Hibernian fever", "HIBERNIAN FEVER, FAMILIAL", "Hibernian fever, familial", "TNF receptor-associated periodic syndrome", "TNF RECEPTOR-ASSOCIATED PERIODIC SYNDROME", "Familial autosomal dominant periodic fever", "Autosomal Dominant Familial Periodic Fever", "autosomal dominant familial periodic fever", "TNF Receptor 1-Associated Periodic Syndrome", "TNF receptor 1-associated periodic syndrome", "periodic FEVER, familial, autosomal dominant", "Periodic fever, familial, autosomal dominant", "PERIODIC FEVER, FAMILIAL, AUTOSOMAL DOMINANT", "TNF receptor-associated periodic fever syndrome", "TNF Receptor-associated Periodic Syndrome (TRAPS)", "TNF receptor-associated periodic fever syndrome (TRAPS)", "TRAPS - TNF receptor-associated periodic fever syndrome", "tumor necrosis factor receptor-associated periodic syndrome", "Tumor necrosis factor receptor-associated periodic syndrome", "TUMOR NECROSIS FACTOR RECEPTOR-ASSOCIATED PERIODIC SYNDROME", "Tumour necrosis factor receptor-associated periodic syndrome", "tumor necrosis factor receptor 1 associated periodic syndrome", "tumor necrosis factor receptor 1-associated periodic syndrome", "Tumor Necrosis Factor Receptor 1-Associated Periodic Syndrome", "Tumor necrosis factor receptor 1 associated periodic syndrome", "Tumor necrosis factor receptor-associated periodic fever syndrome", "Tumour necrosis factor receptor-associated periodic fever syndrome", "Tumor necrosis factor (TNF) receptor-associated periodic fever syndrome", "tumor necrosis factor receptor-associated periodic syndrome (diagnosis)", "Tumour necrosis factor (TNF) receptor-associated periodic fever syndrome", "Tumor necrosis factor receptor-associated periodic fever syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant familial periodic fever", "shortest_name_length": 3}
{"curie": "UMLS:C0423772", "names": ["Sinus;skin", "skin sinus", "Skin sinus", "Skin Sinus", "Skin fistula", "skin fistula", "SKIN FISTULA", "Skin Fistula", "Skin Fistulas", "Fistula, Skin", "skin; fistula", "fistula; skin", "Fistulas, Skin", "Dermal Fistula", "Dermal fistula", "Fistula of Skin", "Fistula of skin", "External Fistula", "External fistula", "external fistula", "fistula external", "External Fistulas", "fistula cutaneous", "cutaneous fistula", "Cutaneous fistula", "Fistula, External", "Cutaneous Fistula", "fistula; cutaneous", "Fistulas, External", "cutaneous; fistula", "Fistula, Cutaneous", "Cutaneous Fistulas", "Fistulas, Cutaneous", "Fistula of skin NOS", "sinus tract of skin", "Fistula of skin, NOS", "Skin sinus (disorder)", "Draining tract of skin", "Dermal Fistula or Sinus", "Fistula of skin (disorder)", "sinus tract of skin (diagnosis)", "External fistula (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous Fistula", "shortest_name_length": 10}
{"curie": "UMLS:C1510428", "names": ["Brain Abscess", "Abscess;cerebral", "cerebral abscess", "Cerebral Abscess", "Cerebral abscess", "cerebral; abscess", "ABSCESS, CEREBRAL", "Abscess, cerebral", "abscess; cerebral", "Abscess, Cerebral", "Cerebral Abscesses", "Abscesses, Cerebral", "Cerebral abscess (disorder)", "Parenchymal intracranial abscess"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebral abscess", "shortest_name_length": 13}
{"curie": "MONDO:0018347", "names": ["IQSEC2-related syndromic intellectual disability", "severe intellectual disability-progressive postnatal microcephaly-midline stereotypic hand movements syndrome", "severe intellectual disability-progressive postnatal microcephaly- midline stereotypic hand movements syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe intellectual disability-progressive postnatal microcephaly- midline stereotypic hand movements syndrome", "shortest_name_length": 48}
{"curie": "MONDO:0003966", "names": ["Testicular Monophasic Choriocarcinoma", "testicular monophasic choriocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular monophasic choriocarcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0012321", "names": ["AD10", "Ad10", "Alzheimer disease 10", "Alzheimer Disease 10", "Alzheimer disease-10", "ALZHEIMER DISEASE 10", "Alzheimer's disease 10", "Alzheimer disease type 10", "Alzheimer's disease type 10", "Alzheimer disease familial 10", "Alzheimer disease, familial, 10", "Alzheimer Disease, Familial, 10", "ALZHEIMER DISEASE, FAMILIAL, 10", "Alzheimer's disease 10, early onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alzheimer disease 10", "shortest_name_length": 4}
{"curie": "UMLS:C1709661", "names": ["Primary FSGS", "Primary Focal Segmental Glomerulosclerosis", "Idiopathic Focal Segmental Glomerulosclerosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Focal Segmental Glomerulosclerosis", "shortest_name_length": 12}
{"curie": "MONDO:0018760", "names": ["DeSanto-Shinawi syndrome", "Chromosome 10p12-p11 deletion syndrome", "WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome", "Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation", "Facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DeSanto-Shinawi syndrome", "shortest_name_length": 24}
{"curie": "UMLS:C1519915", "names": ["Vaginal Adenosquamous Cancer", "Vaginal Adenosquamous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Adenosquamous Carcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0010991", "names": ["laterality defects dominant", "Laterality Defects, Autosomal Dominant", "laterality defects, autosomal dominant", "LATERALITY DEFECTS, AUTOSOMAL DOMINANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laterality defects, autosomal dominant", "shortest_name_length": 27}
{"curie": "UMLS:C0280354", "names": ["Stage III Lip Basal Cell Cancer", "Stage III Lip Basal Cell Carcinoma", "lip basal cell carcinoma, stage III", "Stage III Basal Cell Carcinoma of Lip", "Stage III Basal Cell Carcinoma of the Lip", "stage III basal cell carcinoma of the lip", "basal cell carcinoma of the lip, stage III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Lip Basal Cell Carcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C5419211", "names": ["Unresectable Lung Non-Small Cell Squamous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Lung Non-Small Cell Squamous Carcinoma", "shortest_name_length": 51}
{"curie": "MONDO:0017955", "names": ["granulomatous autoinflammatory syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "granulomatous autoinflammatory syndrome", "shortest_name_length": 39}
{"curie": "MONDO:0043233", "names": ["Erythroderm", "erythroderma", "Eryhtroderma", "ERYTHRODERMA", "Erythroderma", "Erythrodermas", "erythrodermas", "Pityriasis rubra", "pityriasis rubra", "Pityriasis Hebra", "Erythroderma NOS", "Erythrodermatitis", "pityriasis; Hebra", "Hebra; pityriasis", "Hebra's pityriasis", "Papuloerythroderma", "Erythematous eczema", "WILSON-BROCQ DISEASE", "Erythrodermic eczema", "Dermatitis Exfoliativa", "Dermatitis Exfoliative", "exfoliative dermatitis", "Exfoliative Dermatitis", "Exfoliative dermatitis", "dermatitis exfoliative", "DERMATITIS EXFOLIATIVE", "EXFOLIATIVE DERMATITIS", "Dermatitis exfoliative", "dermatitis exfoliativa", "Wilson-Brocq's disease", "Exfoliative dermititis", "Dermatitis, Exfoliative", "exfoliative; dermatitis", "Erythroderma (disorder)", "DERMATITIS, EXFOLIATIVE", "dermatitis; exfoliative", "dermatosis; exfoliativa", "exfoliativa; dermatosis", "Exfoliative, Dermatitis", "Dermatitis Exfoliatives", "exfoliative Dermatitides", "Exfoliative Dermatitides", "Exfoliatives, Dermatitis", "Generalised erythroderma", "ERYTHRODERMA EXFOLIATIVE", "Pityriasis rubra (Hebra)", "erythroderma (diagnosis)", "Generalized erythroderma", "exfoliative erythroderma", "Dermatitides, exfoliative", "Generalised erythrodermia", "Erythroderma, generalized", "Generalized erythrodermia", "ERYTHRODERMA, EXFOLIATIVE", "Pityriasis rubra of Hebra", "Exfoliative dermatitis NOS", "Dermatitis exfoliative NOS", "Erythrodermic eczema (disorder)", "Dermatitis exfoliative generalized", "Generalised exfoliative dermatitis", "Dermatitis Exfoliative Generalized", "Dermatitis exfoliative generalised", "Dermatitis Exfoliative Generalised", "Generalized exfoliative dermatitis", "Exfoliative Generalized, Dermatitis", "Dermatitis Exfoliative Generaliseds", "Pityriasis rubra (Hebra) (disorder)", "Exfoliative Generalised, Dermatitis", "Generalised, Dermatitis Exfoliative", "Exfoliative dermatitis, generalized", "DERMATITIS, EXFOLIATIVE, GENERALIZED", "Red scaly skin caused by inflammatory skin disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exfoliative dermatitis", "shortest_name_length": 11}
{"curie": "MONDO:0019832", "names": ["acquired hypopituitarism", "acquired pituitary hormone deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired pituitary hormone deficiency", "shortest_name_length": 24}
{"curie": "MONDO:0006687", "names": ["BMS", "Orodynia", "stomatodynia", "Stomatodynia", "Stomatopyrosis", "stomatopyrosis", "Oral Dysesthesia", "oral dysesthesia", "Oral dysesthesia", "dysesthesia oral", "Oral dysaesthesia", "oral dysaesthesia", "burning mouth syndrome", "Burning Mouth Syndrome", "Burning mouth syndrome", "Burning Mouth Syndromes", "Syndrome, Burning Mouth", "Mouth Syndrome, Burning", "Mouth Syndromes, Burning", "Syndromes, Burning Mouth", "oral dysesthesia (symptom)", "BMS - Burning mouth syndrome", "BMS - burning mouth syndrome", "Burning mouth syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "burning mouth syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0017799", "names": ["meig syndrome", "Meig Syndrome", "Meigs Syndrome", "Meigs syndrome", "MEIGS SYNDROME", "meigs syndrome", "Meig's Syndrome", "Meigs' Syndrome", "meigs' syndrome", "Meig's syndrome", "Meigs' syndrome", "meig's syndrome", "Meigs-Coss syndrome", "Meigs-Cass syndrome", "Demons-Meigs syndrome", "demons-meigs syndrome", "Meigs' syndrome (disorder)", "Meigs' syndrome (diagnosis)", "Ovarian-ascites-pleural effusion syndrome", "OVARIAN-ASCITES-PLEURAL-EFFUSION SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meigs syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0010853", "names": ["H. pylori infection, susceptibility to", "HELICOBACTER PYLORI INFECTION, SUSCEPTIBILITY TO", "Helicobacter pylori infection, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Helicobacter pylori infection, susceptibility to", "shortest_name_length": 38}
{"curie": "MONDO:0015557", "names": ["Smouldering systemic mastocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Smouldering systemic mastocytosis", "shortest_name_length": 33}
{"curie": "MONDO:0002267", "names": ["obstructed airway", "airway obstructed", "obstruction airway", "Airway obstruction", "airway obstruction", "AIRWAY OBSTRUCTION", "Airway Obstruction", "Embarrassed airway", "airways obstruction", "obstruction; airway", "AIRWAYS OBSTRUCTION", "Obstruction, Airway", "Airway Obstructions", "airway; obstruction", "airway obstructions", "Airways obstruction", "Obstructions, Airway", "Pulmonary obstruction", "Airway obstruction NOS", "Respiratory obstruction", "Airway obstruction, NOS", "respiratory obstruction", "Obstructive Lung Disease", "Obstructive lung disease", "obstruction; respiratory", "obstruction lung disease", "Lung disease obstructive", "DISEASE OBSTRUCTIVE LUNG", "LUNG DISEASE OBSTRUCTIVE", "Disease obstructive lung", "obstructive lung disease", "disease lung obstruction", "disease lung obstructive", "respiratory; obstruction", "OBSTRUCTION LUNG DISEASE", "Obstruction lung disease", "Lung Disease, Obstructive", "obstructive lung diseases", "diseases lung obstruction", "Obstructive Lung Diseases", "Lung Diseases, Obstructive", "AIRWAY DISEASE OBSTRUCTIVE", "Obstructive airway disease", "airway obstructive disease", "obstructive airway disease", "airways disease obstructive", "airway disorder obstructive", "Lungs--Diseases, Obstructive", "Obstructive airways disorder", "obstructive airways disorder", "Obstructive pulmonary disease", "Obstructive Pulmonary Disease", "respiratory airway obstruction", "Pulmonary Disease, Obstructive", "Obstructive Pulmonary Diseases", "Pulmonary Diseases, Obstructive", "Obstructive airways disorder NOS", "Respiratory obstruction (disorder)", "airway obstructed (physical finding)", "obstructive lung disease (generalized)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "obstructive lung disease", "shortest_name_length": 17}
{"curie": "UMLS:C4724169", "names": ["Recurrent Visual Pathway Glioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Visual Pathway Glioma", "shortest_name_length": 31}
{"curie": "MONDO:0100116", "names": ["MERS", "camel flu", "Middle East respiratory syndrome", "Middle East Respiratory Syndrome", "Middle East Respiratory Syndrome (MERS)", "MERS - Middle East respiratory syndrome", "MERS (Middle East Respiratory Syndrome)", "Middle East respiratory syndrome (disorder)", "Middle East Respiratory Syndrome (MERS) (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Middle East respiratory syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0877305", "names": ["Postoperative wound complication", "Postoperative wound complication NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postoperative wound complication", "shortest_name_length": 32}
{"curie": "MONDO:0008290", "names": ["POROK1", "porokeratosis of Mibelli", "porokeratosis 1, MIBELLI type", "porokeratosis 1, Mibelli type", "porokeratosis 1, multiple types"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "porokeratosis 1, Mibelli type", "shortest_name_length": 6}
{"curie": "UMLS:C0278513", "names": ["stage IIIB breast cancer", "Stage IIIB Breast Cancer", "Breast Cancer Stage IIIB", "breast cancer, stage IIIB", "Stage IIIB Breast Carcinoma", "Breast Carcinoma Stage IIIB", "Stage IIIB Breast Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Breast Carcinoma", "shortest_name_length": 24}
{"curie": "UMLS:C4683659", "names": ["Burkitt Lymphoma by Ann Arbor Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Burkitt Lymphoma by Ann Arbor Stage", "shortest_name_length": 35}
{"curie": "UMLS:C1739399", "names": ["Visceral congestion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Visceral congestion", "shortest_name_length": 19}
{"curie": "UMLS:C3899506", "names": ["Congenital Cystic Hygroma", "Cervicofacial Lymphatic Malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Cystic Hygroma", "shortest_name_length": 25}
{"curie": "UMLS:C4683636", "names": ["Adult Hodgkin Lymphoma by Ann Arbor Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Hodgkin Lymphoma by Ann Arbor Stage", "shortest_name_length": 41}
{"curie": "MONDO:0009999", "names": ["RRS", "RRS1", "Covesdem syndrome", "COVESDEM syndrome", "Covesdem syndrome, formerly", "COVESDEM SYNDROME, FORMERLY", "autosomal recessive Robinow syndrome", "Autosomal recessive Robinow syndrome", "Robinow syndrome, autosomal recessive", "ROBINOW SYNDROME, AUTOSOMAL RECESSIVE 1", "Autosomal recessive Robinow syndrome (disorder)", "costovertebral segmentation defect with mesomelia", "Costovertebral segmentation defect-mesomelia syndrome", "costovertebral segmentation defect-mesomelia syndrome", "COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY", "costovertebral segmentation defect with mesomelia, formerly", "ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY", "Robinow syndrome, autosomal recessive, with Brachy-syn-polydactyly", "ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OF PHALANGES AND METACARPALS/METATARSALS", "Robinow syndrome, autosomal recessive, with aplasia/hypoplasia of phalanges and metacarpals/metatarsals"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive Robinow syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C2986963", "names": ["Stage IIIC1 Uterine Corpus Cancer", "Stage IIIC1 Uterine Corpus Cancer AJCC v7", "Stage IIIC1 Uterine (including Endometrial) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC1 Uterine Corpus Cancer AJCC v7", "shortest_name_length": 33}
{"curie": "UMLS:C0233472", "names": ["Labile affect", "affect labile", "Affect Labile", "Labile Affect", "labile affect", "AFFECT LABILE", "Affect lability", "Labile affect (finding)", "labile affect (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Labile affect", "shortest_name_length": 13}
{"curie": "MONDO:0019375", "names": ["MPPH syndrome", "megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome", "megalencephaly, polymicrogyria, and hydrocephalus (MPPH) syndrome", "Megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome", "MPPH (megalencephaly, polymicrogyria, polydactyly, hydrocephalus) syndrome", "megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome", "Megalencephaly, polymicrogyria, postaxial polydactyly, hydrocephalus syndrome", "Megalencephaly, polymicrogyria, postaxial polydactyly, hydrocephalus syndrome (disorder)", "megalencephaly and perisylvian polymicrogyria with postaxial polydactyly and hydrocephalus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome", "shortest_name_length": 13}
{"curie": "UMLS:C0220605", "names": ["Adult NHL", "adult NHL", "NHL, adult", "Non-Hodgkin Lymphoma", "adult non-Hodgkin lymphoma", "Adult Non-Hodgkin Lymphoma", "Non-Hodgkin lymphoma, adult", "Adult Non-Hodgkin's Lymphoma", "adult non-Hodgkin's lymphoma", "non-Hodgkin's lymphoma, adult", "lymphoma, non-Hodgkin's, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Non-Hodgkin Lymphoma", "shortest_name_length": 9}
{"curie": "MONDO:0001798", "names": ["Hypermobility Syndrome", "Hypermobility syndrome", "hypermobility syndrome", "hypermobility syndromes", "syndrome; hypermobility", "hypermobility; syndrome", "Benign joint hypermobility", "benign joint hypermobility", "benign hypermobility joint", "Familial ligamentous laxity", "Joint hypermobility syndrome", "familial; ligamentous laxity", "Hypermobility syndrome (disorder)", "hypermobility syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypermobility syndrome", "shortest_name_length": 22}
{"curie": "UMLS:C0573196", "names": ["cocaine overdose", "overdose cocaine", "of cocaine overdose", "overdose of cocaine", "Overdose of cocaine", "Overdose of cocaine (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Overdose of cocaine", "shortest_name_length": 16}
{"curie": "MONDO:0021002", "names": ["Syndactyly", "syndactyly", "SYNDACTYLY", "syndactylia", "Syndactylia", "symphalangy", "Syndactylus", "Symphalangy", "Syndactylism", "syndactylies", "Syndactylias", "syndactylism", "Syndactylies", "Symphalangism", "Webbed digits", "symphalangism", "Symphalangy NOS", "Webbing of digits", "webbing of digits", "syndactyly (disease)", "Syndactyly (disorder)", "syndactyly (diagnosis)", "Webbed fingers or toes", "Syndactyly, unspecified", "Symphalangism (disorder)", "Congenital webbing of digits", "chromosome 2q35 duplication syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndactyly", "shortest_name_length": 10}
{"curie": "MONDO:0012551", "names": ["AA2", "Alopecia Areata 2", "ALOPECIA AREATA 2", "alopecia areata 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alopecia areata 2", "shortest_name_length": 3}
{"curie": "MONDO:0006397", "names": ["tRCC", "TFE3-Rearranged renal cell carcinoma", "TFE3-Rearranged Renal Cell Carcinoma", "Xp11 Translocation Renal Cell Carcinoma", "translocation-associated renal cell carcinoma", "Xp11.2 translocation-related renal cell carcinoma", "Xp11.2 Translocation-Related Renal Cell Carcinoma", "Renal Cell Cancer Associated with Xp11.2 Translocations/TFE3 Gene Fusions", "renal cell cancer associated with Xp11.2 translocations/TFE3 Gene fusions", "Renal Cell Carcinoma Associated with Xp11.2 Translocations/TFE3 Gene Fusions", "renal cell carcinoma associated with Xp11.2 translocations/TFE3 gene fusions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal cell carcinoma associated with Xp11.2 translocations/TFE3 gene fusions", "shortest_name_length": 4}
{"curie": "MONDO:0005677", "names": ["Rickettsia conorii infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rickettsia conorii infectious disease", "shortest_name_length": 37}
{"curie": "UMLS:C4521867", "names": ["Stage IIA Ampulla of Vater Cancer", "Stage IIA Ampulla of Vater Cancer AJCC v8", "Stage IIA Ampulla of Vater Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Ampulla of Vater Cancer AJCC v8", "shortest_name_length": 33}
{"curie": "MONDO:0016222", "names": ["SCh", "SCH", "Spindle Cell Hemangioma", "spindle-cell hemangioma", "spindle cell hemangioma", "Spindle cell hemangioma", "Spindle cell haemangioma", "spindle -cell hemangioma", "Spindle -Cell Hemangioma", "adult spindle cell hemangioma", "Spindle cell angioendothelioma", "Spindle cell hemangioendothelioma", "spindle cell hemangioendothelioma", "Spindle Cell Hemangioendothelioma", "Spindle cell haemangioendothelioma", "Spindle cell hemangioma (disorder)", "Spindle cell hemangioendothelioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spindle cell hemangioma", "shortest_name_length": 3}
{"curie": "MONDO:0023084", "names": ["epiphyseal dysplasia dysmorphism camptodactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epiphyseal dysplasia dysmorphism camptodactyly", "shortest_name_length": 46}
{"curie": "MONDO:0010567", "names": ["cone dystrophy X-linked with tapetal-like sheen", "Cone dystrophy, x-linked, with tapetal-like sheen", "cone dystrophy, X-linked, with tapetal-like sheen", "CONE DYSTROPHY, X-LINKED, WITH TAPETAL-LIKE SHEEN", "X-linked recessive cone dystrophy with tapetal-like sheen"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cone dystrophy, X-linked, with tapetal-like sheen", "shortest_name_length": 47}
{"curie": "MONDO:0032930", "names": ["IDPOGSA", "intellectual developmental disorder with poor growth and with or without seizures or ataxia", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH POOR GROWTH AND WITH OR WITHOUT SEIZURES OR ATAXIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder with poor growth and with or without seizures or ataxia", "shortest_name_length": 7}
{"curie": "UMLS:C0005942", "names": ["Endocrine Bone Disease", "Disease, Endocrine Bone", "Bone Disease, Endocrine", "Endocrine Bone Diseases", "Diseases, Endocrine Bone", "Bone Diseases, Endocrine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone Diseases, Endocrine", "shortest_name_length": 22}
{"curie": "UMLS:C5669821", "names": ["Recurrent Vaginal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Vaginal Squamous Cell Carcinoma", "shortest_name_length": 41}
{"curie": "UMLS:C0267187", "names": ["gastric intestinal metaplasia", "Intestinal gastric metaplasia", "Gastric intestinal metaplasia", "Gastric Intestinal Metaplasia", "Gastric intestinal metaplasia NOS", "intestinal metaplasia of gastric mucosa", "Intestinal metaplasia of gastric mucosa", "Intestinal Metaplasia of Gastric Mucosa", "Gastric intestinal metaplasia, unspecified", "Intestinal metaplasia of the gastric mucosa", "Intestinal metaplasia of gastric mucosa (disorder)", "intestinal metaplasia of gastric mucosa (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal metaplasia of gastric mucosa", "shortest_name_length": 29}
{"curie": "UMLS:C1301356", "names": ["RCMD-RS", "RCMD RS", "MDS-RS-MLD", "Refractory Cytopenia with Multilineage Dysplasia and Ring Sideroblasts", "Refractory cytopenia with multilineage dysplasia and ring sideroblasts", "Refractory cytopenia with multilineage dysplasia and ringed sideroblasts", "refractory cytopenia with multilineage dysplasia and ringed sideroblasts", "Refractory Cytopenia with Multilineage Dysplasia and Ringed Sideroblasts", "Refractory cytopaenia with multilineage dysplasia and ringed sideroblasts", "Myelodysplastic syndrome with ring sideroblasts and multilineage dysplasia", "Myelodysplastic Syndrome with Ring Sideroblasts and Multilineage Dysplasia", "refractory cytopenia with multilineage dysplasia and ringed sideroblasts (diagnosis)", "Myelodysplastic syndrome with ring sideroblasts and multilineage dysplasia (disorder)", "Myelodysplastic syndrome with ring sideroblasts and multilineage dysplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myelodysplastic syndrome with ring sideroblasts and multilineage dysplasia", "shortest_name_length": 7}
{"curie": "MONDO:0000148", "names": ["pulmonary fibrosis and/or bone marrow failure, telomere-related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary fibrosis and/or bone marrow failure, telomere-related", "shortest_name_length": 63}
{"curie": "MONDO:0007526", "names": ["PDS", "EDSSPD1", "B4GALT7-CDG", "XGPT deficiency", "EDS, progeroid type", "dermatan sulfate proteoglycan", "Pds, defective biosynthesis of", "galactosyltransferase I deficiency", "galactosyltransferase 1 deficiency", "Ehlers-Danlos syndrome progeroid type", "Ehlers-Danlos syndrome, progeroid type", "Ehlers-Danlos syndrome, progeroid form", "EHLERS-DANLOS SYNDROME, PROGEROID FORM", "EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 2", "spondylodysplastic Ehlers-Danlos syndrome", "Ehlers-Danlos syndrome, spondylodysplastic type", "Ehlers-Danlos syndrome, progeroid type (former)", "Ehlers-Danlos syndrome spondylodysplastic type 2", "defective biosynthesis of proteodermatan sulfate", "Ehlers-Danlos syndrome progeroid type (disorder)", "proteodermatan sulfate, defective biosynthesis of", "Ehlers-Danlos syndrome, spondylodysplastic type, 1", "xylosylprotein 4-beta-galactosyltransferase deficiency", "Ehlers-Danlos syndrome with short stature and limb anomalies", "B4GALT7-related spondylodysplastic EDS (Ehlers-Danlos syndrome)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ehlers-Danlos syndrome, spondylodysplastic type", "shortest_name_length": 3}
{"curie": "MONDO:0013014", "names": ["SEMDAG", "SEMD, AGGRECAN TYPE", "SEMD, Aggrecan Type", "SEMD, aggrecan type", "Spondyloepimetaphyseal dysplasia aggrecan type", "spondyloepimetaphyseal dysplasia, aggrecan type", "Spondyloepimetaphyseal Dysplasia, Aggrecan Type", "Spondyloepimetaphyseal dysplasia, aggrecan type", "SPONDYLOEPIMETAPHYSEAL DYSPLASIA, AGGRECAN TYPE", "Spondyloepimetaphyseal dysplasia aggrecan type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepimetaphyseal dysplasia, aggrecan type", "shortest_name_length": 6}
{"curie": "MONDO:0005794", "names": ["infection herpes", "herpes infection", "HERPES INFECTION", "Herpes infection", "Herpes infections", "herpes infections", "herpes virus disease", "disease herpes virus", "herpesvirus infection", "Herpesvirus Infection", "diseases herpes virus", "Herpesvirus infection", "Herpes infection, NOS", "Herpesviridae disease", "Herpesvirus infections", "infection, Herpesvirus", "Herpes virus infection", "herpes virus infection", "viral infection herpes", "Herpesvirus Infections", "Infection, Herpesvirus", "herpes viral infection", "herpesviridae infection", "Herpesviridae Infection", "Infections, Herpesvirus", "Herpes viral infections", "infections, Herpesvirus", "Herpesviridae infection", "infection, Herpesviridae", "Herpesviridae infections", "Infection, Herpesviridae", "Herpesviridae Infections", "Infections, Herpesviridae", "infections, Herpesviridae", "Herpesvirus infection, NOS", "Herpes viral infection NOS", "DISEASES DUE TO HERPESVIRIDAE", "Herpesvirus infection (disorder)", "Herpesviridae infectious disease", "Herpesviridae disease or disorder", "Herpesviridae caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Herpesviridae infectious disease", "shortest_name_length": 16}
{"curie": "MONDO:0007945", "names": ["PHOSPHODIESTER GLYCOSIDE DEFICIENCY", "phosphodiester glycoside deficiency", "Phosphodiester Glycoside Deficiency", "MANNOSE 6-PHOSPHATE RECEPTOR RECOGNITION DEFECT, LEBANESE TYPE", "Mannose 6-Phosphate Receptor Recognition Defect, Lebanese Type", "mannose 6-phosphate receptor recognition defect, Lebanese type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mannose 6-phosphate receptor recognition defect, Lebanese type", "shortest_name_length": 35}
{"curie": "MONDO:0030118", "names": ["SRS4", "SILVER-RUSSELL SYNDROME 4", "silver-russell syndrome 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "silver-russell syndrome 4", "shortest_name_length": 4}
{"curie": "MONDO:0007723", "names": ["MGC", "HSCR", "HSCR1", "HIRSCHSPRUNG DISEASE", "Hirschsprung disease", "aganglionic megacolon", "AGANGLIONIC MEGACOLON", "Hirschsprung disease 1", "megacolon, aganglionic", "MEGACOLON, AGANGLIONIC", "RET Hirschsprung disease", "Hirschsprung disease type 1", "HIRSCHSPRUNG DISEASE, PROTECTION AGAINST", "susceptibility to Hirschsprung disease 1", "Hirschsprung disease, protection against", "Hirschsprung disease, susceptibility to, 1", "HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1", "Hirschsprung disease caused by mutation in RET", "Hirschsprung disease, susceptibility to, type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hirschsprung disease, susceptibility to, 1", "shortest_name_length": 3}
{"curie": "MONDO:0009497", "names": ["Vitsala", "kifafa seizure disorder", "Kifafa seizure disorder", "KIFAFA SEIZURE DISORDER", "Complex familial seizure disorder", "parkinsonian features and neurologic abnormalities, mental retardation and transient psychotic episodes", "parkinsonian features and neurologic abnormalities, intellectual disability and transient psychotic episodes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kifafa seizure disorder", "shortest_name_length": 7}
{"curie": "MONDO:0002631", "names": ["COS", "Central", "central osteosarcoma", "Central Osteosarcoma", "Central osteosarcoma", "Medullary osteosarcoma", "Medullary Osteosarcoma", "medullary osteosarcoma", "anaplastic osteosarcoma", "Anaplastic osteosarcoma", "osteosarcoma, anaplastic", "conventional osteosarcoma", "Conventional Osteosarcoma", "Intracortical osteosarcoma", "intracortical osteosarcoma", "Intracortical Osteosarcoma", "anaplastic osteogenic sarcoma", "undifferentiated osteosarcoma", "sarcoma, osteogenic anaplastic", "osteogenic sarcoma, anaplastic", "osteosarcoma, undifferentiated", "intracortical osteogenic sarcoma", "Intracortical Osteogenic Sarcoma", "undifferentiated sarcoma of bone", "Conventional Central Osteosarcoma", "conventional central osteosarcoma", "Conventional central osteosarcoma", "undifferentiated osteogenic sarcoma", "sarcoma, osteogenic undifferentiated", "osteogenic sarcoma, undifferentiated", "undifferentiated sarcoma of bone (diagnosis)", "Central osteosarcoma (morphologic abnormality)", "intracortical osteosarcoma (morphologic abnormality)", "Intracortical osteosarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "conventional osteosarcoma", "shortest_name_length": 3}
{"curie": "UMLS:C0235573", "names": ["hemoglobinemia", "Hemoglobinemia", "HEMOGLOBINEMIA", "HAEMOGLOBINAEMIA", "Haemoglobinaemia", "Hemoglobinemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemoglobinemia", "shortest_name_length": 14}
{"curie": "MONDO:0040732", "names": ["Infection due to Pseudomonas aeruginosa", "infection due to Pseudomonas aeruginosa", "Pseudomonas aeruginosa infectious disease", "Infection caused by Pseudomonas aeruginosa", "infection caused by Pseudomonas aeruginosa", "Infection caused by Pseudomonas aeruginosa (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pseudomonas aeruginosa infectious disease", "shortest_name_length": 39}
{"curie": "UMLS:C0855109", "names": ["Burkitt's tumor stage IV", "Burkitt's tumour stage IV", "Stage IV Burkitt Lymphoma", "Burkitt's Lymphoma Stage IV", "Stage IV Burkitt's Lymphoma", "Burkitt's lymphoma stage IV", "Ann Arbor Stage IV Burkitt Lymphoma", "Burkitt's tumor or lymphoma stage IV", "Burkitt's tumour or lymphoma stage IV"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Burkitt Lymphoma", "shortest_name_length": 24}
{"curie": "MONDO:0017418", "names": ["CIF", "chronic intestinal failure", "Chronic intestinal failure", "Chronic failure of small intestine", "Type III chronic intestinal failure", "Chronic failure of small intestine (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic intestinal failure", "shortest_name_length": 3}
{"curie": "UMLS:C0151971", "names": ["ulcer; bowel", "bowel; ulcer", "bowel; erosion", "erosion; bowel", "intestine ulcer", "ulcer intestine", "intestinal ulcer", "Intestinal Ulcer", "intestine ulcers", "ULCER INTESTINAL", "INTESTINAL ULCER", "Intestinal ulcer", "Ulcer intestinal", "ulcer; intestine", "intestinal ulcers", "intestinal; ulcer", "Ulcer of intestine", "Intestine ulceration", "Intestinal ulceration", "INTESTINAL ULCERATION", "ulceration of intestine", "Ulceration of intestine", "Intestinal ulceration NOS", "Primary ulcer of intestine", "Ulceration of intestine, NOS", "Primary ulcer of intestine, NOS", "Ulceration of intestine (disorder)", "ulceration of intestine (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ulceration of intestine", "shortest_name_length": 12}
{"curie": "UMLS:C0278762", "names": ["DHL, adult", "adult DL lymphoma", "DL lymphoma, adult", "Diffuse Large Cell Lymphoma", "Adult Diffuse Large Cell Lymphoma", "Diffuse Large Cell Adult Lymphoma", "adult diffuse large cell lymphoma", "diffuse large cell lymphoma, adult", "Adult Diffuse Histiocytic Lymphoma", "Diffuse Histiocytic Adult Lymphoma", "large cell lymphoma, diffuse, adult", "lymphoma, diffuse large cell, adult", "diffuse histiocytic lymphoma, adult", "lymphoma, diffuse histiocytic, adult", "histiocytic lymphoma, diffuse, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Diffuse Large Cell Lymphoma", "shortest_name_length": 10}
{"curie": "UMLS:C4331427", "names": ["Transient Primary Hypothyroidism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transient Primary Hypothyroidism", "shortest_name_length": 32}
{"curie": "MONDO:0014710", "names": ["IMD42", "IMMUNODEFICIENCY 42", "immunodeficiency 42", "immunodeficiency type 42", "autosomal recessive primary immunodeficiency due to RORC mutation", "Autosomal recessive primary immunodeficiency due to RORC mutation", "Autosomal recessive MSMD due to complete RORgamma receptor defiency", "autosomal recessive MSMD due to complete RORgamma receptor defiency", "RORC autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency", "Autosomal recessive mendelian susceptibility to mycobacterial disease due to complete RORgamma receptor mutation", "Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency", "autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency", "Autosomal recessive MSMD (mendelian susceptibility to mycobacterial disease) due to complete RORgamma receptor mutation", "autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency caused by mutation in RORC", "Autosomal recessive mendelian susceptibility to mycobacterial disease due to complete RAR related orphan receptor C receptor mutation", "Autosomal recessive mendelian susceptibility to mycobacterial disease due to complete RAR related orphan receptor C receptor mutation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0001988", "names": ["External resorption of tooth", "Resorption of teeth (external)", "external pathological resorption", "Pathological resorption, external", "External resorption of root of tooth", "External resorption of tooth (disorder)", "pathological resorption of external root", "Pathological tooth resorption - external", "Pathological resorption of tooth external", "external pathological resorption (diagnosis)", "pathological resorption of external root (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "external pathological resorption", "shortest_name_length": 28}
{"curie": "MONDO:0044343", "names": ["Cervical disc degeneration", "degeneration cervical disc", "cervical disc degeneration", "Disc degeneration;cervical", "cervical Disc Degeneration", "Cervical Disc Degeneration", "Cervical Disc Degenerative Disease", "cervical Disc degenerative disease", "cervical disc degenerative disorder", "cervical Disc degenerative disorder", "Cervical Disc Degenerative Disorder", "cervical disc degeneration (diagnosis)", "degeneration; intervertebral disc, cervical", "intervertebral disc degeneration - cervical", "Degeneration of cervical intervertebral disc", "degeneration of cervical intervertebral disc", "Degeneration of cervical intervertebral disc (disorder)", "cervical region of vertebral column intervertebral disc degenerative disorder", "intervertebral disc degenerative disorder of cervical region of vertebral column"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical disc degenerative disorder", "shortest_name_length": 26}
{"curie": "MONDO:0044912", "names": ["spinal cord metastases", "SPINAL CORD METASTASIS", "cord metastasis spinal", "spinal cord metastasis", "Metastasis to Spinal Cord", "metastasis to spinal cord", "Metastases to spinal cord", "Metastasis to spinal cord", "Metastatic tumor to the spinal cord", "Metastatic Tumor to the Spinal Cord", "Metastatic neoplasm to the spinal cord", "Metastatic Neoplasm to the Spinal Cord", "neoplasm - spinal cord malignant secondary", "Secondary malignant neoplasm of spinal cord", "Metastatic malignant neoplasm of spinal cord", "Secondary Malignant Tumor to the Spinal Cord", "Metastatic malignant neoplasm to spinal cord", "Secondary malignant tumor to the spinal cord", "Secondary malignant neoplasm to the spinal cord", "Secondary Malignant Neoplasm to the Spinal Cord", "Metastatic Malignant Neoplasm in the Spinal Cord", "Metastatic Malignant Neoplasm to the Spinal Cord", "Metastatic malignant neoplasm to the spinal cord", "metastatic malignant neoplasm in the spinal cord", "Metastatic malignant neoplasm in the spinal cord", "Metastatic malignant neoplasm to spinal cord (disorder)", "Secondary malignant neoplasm of spinal cord (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metastatic malignant neoplasm in the spinal cord", "shortest_name_length": 22}
{"curie": "MONDO:0020857", "names": ["ODG7", "ovarian dysgenesis 7", "OVARIAN DYSGENESIS 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian dysgenesis 7", "shortest_name_length": 4}
{"curie": "UMLS:C5205621", "names": ["Chronic Cutaneous GvHD", "Chronic Cutaneous Graft Versus Host Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic Cutaneous Graft Versus Host Disease", "shortest_name_length": 22}
{"curie": "UMLS:C5420821", "names": ["Refractory Vulvar Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Vulvar Carcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0015345", "names": ["POMA", "Perioral myoclonia with absences", "perioral myoclonia with absences", "POMA - perioral myoclonia with absences", "Perioral myoclonia with absences (disorder)", "Perioral myoclonia with absences (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "perioral myoclonia with absences", "shortest_name_length": 4}
{"curie": "UMLS:C0003257", "names": ["antibody deficiency syndrome", "Antibody Deficiency Syndrome", "syndrome; antibody deficiency", "antibody deficiency; syndrome", "Deficiency Syndrome, Antibody", "Antibody Deficiency Syndromes", "Syndrome, Antibody Deficiency", "Syndromes, Antibody Deficiency", "Deficiency Syndromes, Antibody"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Antibody Deficiency Syndrome", "shortest_name_length": 28}
{"curie": "UMLS:C2930830", "names": ["Kidney disorder involving deposition of calcium and oxalate or phosphate in the renal tubules"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kidney disorder involving deposition of calcium and oxalate or phosphate in the renal tubules", "shortest_name_length": 93}
{"curie": "EFO:1002009", "names": ["macular telangiectasia type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macular telangiectasia type 2", "shortest_name_length": 29}
{"curie": "MONDO:0017620", "names": ["CSID without starch intolerance", "disaccharide intolerance without starch intolerance", "congenital sucrose intolerance without starch intolerance", "congenital sucrase-isomaltase deficiency without starch intolerance", "congenital sucrase-isomaltose malabsorption without starch intolerance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital sucrase-isomaltase deficiency without starch intolerance", "shortest_name_length": 31}
{"curie": "UMLS:C1142028", "names": ["Peripheral nerve palsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peripheral nerve palsy", "shortest_name_length": 22}
{"curie": "MONDO:0004015", "names": ["pineal area teratoma", "Pineal Area Teratoma", "pineal region teratoma", "Pineal Region Teratoma", "Teratoma of Pineal Area", "teratoma of Pineal Area", "teratoma of pineal area", "teratoma of pineal region", "Teratoma of Pineal Region", "teratoma of the pineal area", "Teratoma of the Pineal Area", "teratoma of the pineal region", "Teratoma of the Pineal Region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pineal region teratoma", "shortest_name_length": 20}
{"curie": "MONDO:0008254", "names": ["platelet disorder, undefined", "PLATELET DISORDER, UNDEFINED", "Platelet Disorder, Undefined"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "platelet disorder, undefined", "shortest_name_length": 28}
{"curie": "UMLS:C4521880", "names": ["stage IA pleural mesothelioma", "stage IA malignant mesothelioma", "stage IA pleural mesothelioma AJCC v7", "Stage IA Pleural Malignant Mesothelioma", "Stage IA Pleural Malignant Mesothelioma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Pleural Malignant Mesothelioma AJCC v7", "shortest_name_length": 29}
{"curie": "MONDO:0003969", "names": ["amphetamine abuse", "Amphetamine-related disorder", "Disorder, Amphetamine-Related", "Amphetamine Related Disorders", "Amphetamine-Related Disorders", "amphetamine-related disorders", "Disorders, Amphetamine-Related", "Amphetamine-related disorder, NOS", "Amphetamine induced mental disorder", "amphetamine-related disorders (diagnosis)", "Amphetamine-induced organic mental disorder", "Amphetamine-induced organic mental disorder, NOS", "Amphetamine or related acting sympathomimetic abuse", "Organic mental disorder caused by amphetamine and/or amfetamine derivative", "Organic mental disorder caused by amphetamine and/or amfetamine derivative (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amphetamine abuse", "shortest_name_length": 17}
{"curie": "MONDO:0014700", "names": ["AUKS", "AU-KLINE SYNDROME", "Au Kline syndrome", "Au-Kline syndrome", "AU-Kline syndrome", "Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome", "Neurodevelopmental disorder, craniofacial dysmorphism, cardiac defect, skeletal anomalies syndrome", "Neurodevelopmental disorder, craniofacial dysmorphism, cardiac defect, skeletal anomalies syndrome (disorder)", "neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome due to a point mutation", "Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome due to a point mutation", "shortest_name_length": 4}
{"curie": "MONDO:0040923", "names": ["late latent syphilis", "SYPHILIS LATENT LATE", "Late latent syphilis", "Late Latent Syphilis", "latent late syphilis", "Late syphilis, latent", "syphilis; late, latent", "Late latent syphilis (disorder)", "latent late syphilis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "late latent syphilis", "shortest_name_length": 20}
{"curie": "UMLS:C4521731", "names": ["Stage II Esophageal Squamous Cell Cancer", "Postneoadjuvant Therapy Stage II Esophageal Squamous Cell Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postneoadjuvant Therapy Stage II Esophageal Squamous Cell Carcinoma AJCC v8", "shortest_name_length": 40}
{"curie": "MONDO:0010300", "names": ["MRX53", "XLID53", "X-linked mental retardation 53", "Mental Retardation, X-Linked 53", "mental retardation, X-linked 53", "MENTAL RETARDATION, X-LINKED 53", "intellectual disability, X-linked 53", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 53", "non-syndromic X-linked intellectual disability 53", "mental retardation, X-linked 53, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 53", "shortest_name_length": 5}
{"curie": "MONDO:0000494", "names": ["renal fibrosis", "Renal fibrosis", "Kidney fibrosis", "fibrosis kidney", "FIBROSIS KIDNEY", "kidney fibrosis", "Fibrosis kidney", "KIDNEY FIBROSIS", "fibrosis kidneys", "fibrosis; kidney", "kidney; fibrosis", "Renal fibrosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal fibrosis", "shortest_name_length": 14}
{"curie": "UMLS:C4764039", "names": ["Advanced Digestive System Neuroendocrine Neoplasm", "Advanced Gastroenteropancreatic Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Digestive System Neuroendocrine Neoplasm", "shortest_name_length": 49}
{"curie": "MONDO:0009655", "names": ["MPS3A", "MPS 3A", "mp iii", "MPSIIIA", "MPS 3 A", "mps iii", "MPS IIIA", "MPS III A", "MPS III-A", "Sanfilippo A", "Sanfilippo A syndrome", "Sanfilippo Syndrome A", "Sanfilippo syndrome A", "SANFILIPPO SYNDROME A", "Sanfilippo syndrome a", "Sulfamidase Deficiency", "sulfamidase deficiency", "SULFAMIDASE DEFICIENCY", "Deficiency, Sulfamidase", "Sulfamidase Deficiencies", "Deficiencies, Sulfamidase", "sanfilippo syndrome type a", "Sanfilippo syndrome type A", "type A Sanfilippo syndrome", "Sanfilippo syndrome, type A", "Mucopolysaccharidosis III-A", "mucopolysaccharidosis III-A", "Mucopolysaccharidosis type 3A", "mucopolysaccharidosis type 3A", "Mucopolysaccharidosis Type 3 A", "heparan sulfamidase deficiency", "Heparan sulfamidase deficiency", "Heparan-N-sulfatase deficiency", "mucopolysaccharidosis, type 3A", "mucopoly-saccharidosis type 3A", "Mucopolysaccharidosis Type IIIA", "Heparan-N-sulphatase deficiency", "heparane sulfamidase deficiency", "mucopolysaccharidosis type IIIA", "Mucopolysaccharidosis type IIIA", "Heparan sulphamidase deficiency", "mucopolysaccharidosis type III-A", "Mucopolysaccharidosis Type IIIAs", "mucopolysaccharidosis, type IIIA", "Mucopolysaccharidosis, type IIIA", "MUCOPOLYSACCHARIDOSIS, TYPE IIIA", "Mucopolysaccharidosis, MPS-III-A", "Heparan sulfate sulfatase deficiency", "Heparan Sulfate Sulfatase Deficiency", "heparan sulfate sulfatase deficiency", "HEPARAN SULFATE SULFATASE DEFICIENCY", "Mucopolysaccharidosis III-A (disorder)", "Heparan sulphate sulphatase deficiency", "MPS III-A - Mucopolysaccharidosis III-A", "MPSIIIA - Mucopolysaccharidosis type IIIA", "N-sulfoglucosamine sulfohydrolase deficiency", "mucopolysaccharidosis type III-A (diagnosis)", "N-sulphoglucosamine sulphohydrolase deficiency", "mucopolysaccharidosis type IIIA (Sanfilippo A)", "Mucopolysaccharidosis Type 3 A Sanfilippo Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucopolysaccharidosis type 3A", "shortest_name_length": 5}
{"curie": "MONDO:0007123", "names": ["AFA", "Ankyloblepharon", "ankyloblepharon", "Eyelid synechiae", "Adhesion of eyelids", "Eyelids stuck together", "Ankyloblepharon (disorder)", "Ankyloblepharon filiforme adnatum", "ankyloblepharon filiforme adnatum", "ankyloblepharon (physical finding)", "ankyloblepharon filiforme congenitum", "Ankyloblepharon filiforme congenitum", "Isolated ankyloblepharon filiforme adnatum", "Ankyloblepharon filiforme adnatum (disorder)", "ankyloblepharon filiforme adnatum cleft palate", "Ankyloblepharon filiforme adnatum cleft palate", "Ankyloblepharon filiforme adnatum and cleft palate", "ANKYLOBLEPHARON FILIFORME ADNATUM AND CLEFT PALATE", "Ankyloblepharon Filiforme Adnatum and Cleft Palate", "ankyloblepharon filiforme adnatum and cleft palate", "Ankyloblepharon filiforme adnatum-cleft palate syndrome", "ankyloblepharon filiforme adnatum-cleft palate syndrome", "Ankyloblepharon filiforme adnatum with cleft palate syndrome", "Ankyloblepharon filiforme adnatum with cleft palate syndrome (disorder)", "Congenital filiform fusion of the eyelids with cleft palate and-or cleft lip", "congenital filiform fusion of the eyelids with cleft palate and/or cleft lip"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ankyloblepharon filiforme adnatum-cleft palate syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0018472", "names": ["TCMGLY", "long eyelashes", "Familial isolated trichomegaly", "familial isolated trichomegaly", "Familial isolated trichomegaly (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial isolated trichomegaly", "shortest_name_length": 6}
{"curie": "UMLS:C0264309", "names": ["vocal cord disease", "vocal cord disorder", "Vocal Cord Disorder", "Vocal cord disorder", "cord disorders vocal", "Disorder of vocal cord", "Vocal cord disorder NOS", "Disease of vocal cords, NOS", "vocal cord disorder (diagnosis)", "Disorder of vocal cord (disorder)", "Disease or syndrome of vocal cords"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disorder of vocal cord", "shortest_name_length": 18}
{"curie": "OMIM:617970", "names": ["RHNA", "RH-NULL, AMORPH TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 4}
{"curie": "UMLS:C5420824", "names": ["Refractory Acute Monoblastic and Monocytic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Acute Monoblastic and Monocytic Leukemia", "shortest_name_length": 51}
{"curie": "MONDO:0019610", "names": ["ZES", "Gastrinoma", "gastrinoma", "Z-E SYNDROME", "syndrome z-e", "z-e syndrome", "Z E syndrome", "Z-E syndrome", "Zollinger-Ellison", "Ellison-Zollinger", "gastrinoma syndrome", "syndrome gastrinoma", "Gastrinoma syndrome", "zollinger-ellison syndrome", "SYNDROME ZOLLINGER ELLISON", "ellison syndrome zollinger", "Zollinger-Ellison Syndrome", "ZOLLINGER ELLISON SYNDROME", "Zollinger-Ellison syndrome", "zollinger ellison syndrome", "Zollinger Ellison Syndrome", "Syndrome Zollinger Ellison", "syndrome zollinger-ellison", "Zollinger Ellison syndrome", "ZOLLINGER-ELLISON SYNDROME", "syndrome zollinger ellison", "Excessive gastrin secretion", "syndrome zollinger ellisons", "Syndrome, Zollinger-Ellison", "ZE - Zollinger-Ellison syndrome", "Zollinger-Ellison syndrome (disease)", "Zollinger-Ellison syndrome (disorder)", "pancreatic ulcerogenic tumor syndrome", "PANCREATIC ULCEROGENIC TUMOR SYNDROME", "ulcerogenic tumor of the pancreas syndrome", "peptic ulcer due to Zollinger Ellison syndrome", "peptic ulcer due to Zollinger Ellison syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Zollinger-Ellison syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0017530", "names": ["polysyndactyly, bilateral", "preaxial polydactyly type 4, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polysyndactyly, bilateral", "shortest_name_length": 25}
{"curie": "OMIM:606771", "names": ["CAQ14", "ADIPQTL3", "ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 3", "CIRCULATING ADIPONECTIN QUANTITATIVE TRAIT LOCUS ON CHROMOSOME 14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 5}
{"curie": "MONDO:0011461", "names": ["FEB3A", "GEFSP2", "GEFS+2", "GEFS, Type 2", "Gefs+, type 2", "GEFS+, TYPE 2", "febrile seizures, familial, 3A", "Seizures, Familial Febrile, 3a", "FEBRILE SEIZURES, FAMILIAL, 3A", "Febrile Seizures, Familial, 3A", "SCN1A febrile seizures, familial", "Febrile Convulsions, Familial, 3a", "Convulsions, Familial Febrile, 3a", "generalized epilepsy with febrile seizures plus 2", "generalised epilepsy with febrile seizures plus 2", "generalised epilepsy with febrile seizures plus type 2", "generalized epilepsy with febrile seizures plus type 2", "febrile seizures, familial caused by mutation in SCN1A", "Generalized Epilepsy With Febrile Seizures Plus, Type 2", "generalized epilepsy with febrile seizures plus, type 2", "GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "generalized epilepsy with febrile seizures plus, type 2", "shortest_name_length": 5}
{"curie": "MONDO:0008772", "names": ["Ai2a1", "AI2A1", "KLK4 amelogenesis imperfecta", "amelogenesis imperfecta type 2A1", "amelogenesis imperfecta type IIA1", "amelogenesis imperfecta, type IIA1", "amelogenesis imperfecta, hypomaturation type, IIA1", "Amelogenesis Imperfecta, Hypomaturation Type, Iia1", "amelogenesis imperfecta caused by mutation in KLK4", "AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA1", "amelogenesis imperfecta pigmented hypomaturation type", "Amelogenesis imperfecta pigmented hypomaturation type", "Amelogenesis imperfecta, pigmented hypomaturation type", "amelogenesis imperfecta pigmented hypomaturation type 1", "amelogenesis imperfecta, pigmented hypomaturation type, 1", "Amelogenesis Imperfecta, Pigmented Hypomaturation Type, 1", "AMELOGENESIS IMPERFECTA, PIGMENTED HYPOMATURATION TYPE, 1", "Amelogenesis imperfecta, pigmented hypomaturation type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amelogenesis imperfecta type 2A1", "shortest_name_length": 5}
{"curie": "MONDO:0042974", "names": ["PIV3", "human parainfluenza virus type 3", "Infection due to Parainfluenza virus 3", "infection due to parainfluenza virus 3", "human respirovirus 3 infectious disease", "human respirovirus 3 disease or disorder", "infection caused by parainfluenza virus 3", "Infection caused by Parainfluenza virus 3", "Infection due to Human parainfluenza virus 3", "infection due to human parainfluenza virus 3", "parainfluenza virus type 3 infectious disease", "infection caused by human parainfluenza virus 3", "human respirovirus 3 caused disease or disorder", "Infection caused by Human parainfluenza virus 3", "Infection caused by Human parainfluenza virus 3 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parainfluenza virus type 3 infectious disease", "shortest_name_length": 4}
{"curie": "MONDO:0011694", "names": ["SCA15", "SCAR16", "SCA15/16", "SCA16, FORMERLY", "SCA16 (formerly)", "Spinocerebellar Ataxia 15", "spinocerebellar ataxia 16", "spinocerebellar ataxia 15", "SPINOCEREBELLAR ATAXIA 15", "spinocerebellar ataxia type 16", "spinocerebellar ataxia type 15", "Spinocerebellar Ataxia Type 16", "SCA15 Spinocerebellar Ataxia 15", "spinocerebellar ataxia type 15/16", "Spinocerebellar ataxia type 15/16", "spinocerebellar ataxia 16, formerly", "SPINOCEREBELLAR ATAXIA 16, FORMERLY", "spinocerebellar ataxia 16 (formerly)", "Spinocerebellar ataxia type 15/16 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia type 15/16", "shortest_name_length": 5}
{"curie": "MONDO:0006807", "names": ["perforated bowel", "PEFORATION BOWEL", "bowel perforated", "Perforated bowel", "BOWEL PERFORATION", "Bowel Perforation", "bowel perforation", "bowels perforated", "Bowel perforation", "Perforation bowel", "bowel; perforation", "perforation; bowel", "bowel perforations", "intestine perforation", "Intestinal perforation", "intestinal perforation", "INTESTINE, PERFORATION", "Perforation intestinal", "INTESTINAL PERFORATION", "perforation intestinal", "intestines perforation", "PERFORATION INTESTINAL", "Intestinal Perforation", "Intestinal Perforations", "Perforation, Intestinal", "intestinal perforations", "Perforation of intestine", "Perforation of Intestine", "Perforations, Intestinal", "perforation of intestine", "Intestinal perforation NOS", "Perforation of intestine, NOS", "intestinal perforation (diagnosis)", "Perforation of intestine (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intestinal perforation", "shortest_name_length": 16}
{"curie": "UMLS:C4528751", "names": ["Leukemic Nonnodal Mantle Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leukemic Nonnodal Mantle Cell Lymphoma", "shortest_name_length": 38}
{"curie": "MONDO:0014979", "names": ["NEIMY", "MYOCLONUS, INTRACTABLE, NEONATAL", "myoclonus, intractable, neonatal", "myoclonus, intractable, neonatal; NEIMY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myoclonus, intractable, neonatal", "shortest_name_length": 5}
{"curie": "MONDO:0017700", "names": ["GSDIV, childhood neuromuscular form", "GSD IV, NEUROMUSCULAR FORM, CHILDHOOD", "GSD IV, Neuromuscular Form, Childhood", "GSD type 4, childhood neuromuscular form", "GBE deficiency, childhood neuromuscular form", "glycogenosis type 4, childhood neuromuscular form", "Glycogenosis type 4, childhood neuromuscular form", "glycogenosis type IV, childhood neuromuscular form", "Glycogenosis type IV, childhood neuromuscular form", "Glycogen storage disease type 4, childhood neuromuscular form", "glycogen storage disease type 4, childhood neuromuscular form", "Glycogen storage disease type IV, childhood neuromuscular form", "glycogen storage disease type IV, childhood neuromuscular form", "GSD due to glycogen branching enzyme deficiency, childhood neuromuscular form", "glycogenosis due to glycogen branching enzyme deficiency, childhood neuromuscular form", "Glycogenosis due to glycogen branching enzyme deficiency, childhood neuromuscular form", "glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form", "Glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form", "shortest_name_length": 35}
{"curie": "UMLS:C4683615", "names": ["Childhood Lymphoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Lymphoma by AJCC v8 Stage", "shortest_name_length": 35}
{"curie": "MONDO:0013765", "names": ["CHDS6", "MMP3 coronary artery disease", "susceptibility to coronary heart disease 6", "coronary heart disease, susceptibility to, 6", "CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 6", "coronary heart disease, susceptibility to, type 6", "coronary artery disease caused by mutation in MMP3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coronary heart disease, susceptibility to, 6", "shortest_name_length": 5}
{"curie": "MONDO:0004273", "names": ["Breast Apocrine Adenoma", "breast apocrine adenoma", "apocrine; adenoma, breast", "apocrine adenoma of breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast apocrine adenoma", "shortest_name_length": 23}
{"curie": "MONDO:0010454", "names": ["MRX88", "XLID88", "X-linked mental retardation 88", "MENTAL RETARDATION, X-LINKED 88", "mental retardation, X-linked 88", "intellectual disability, X-linked 88", "intellectual disability, XMEN-linked 88", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 88", "non-syndromic X-linked intellectual disability 88"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 88", "shortest_name_length": 5}
{"curie": "UMLS:C4764394", "names": ["Transformed Small Lymphocytic Lymphoma to Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transformed Small Lymphocytic Lymphoma to Diffuse Large B-Cell Lymphoma", "shortest_name_length": 71}
{"curie": "MONDO:0005303", "names": ["Drug Addiction", "Drug addiction", "drug addiction", "DRUG ADDICTION", "addiction drug", "Addiction, Drug", "DRUG DEPENDENCE", "Drug dependency", "drug dependency", "Drug Dependency", "drugs addiction", "dependence drug", "Drug Dependence", "addictions drug", "dependency drug", "drug dependence", "Drug dependence", "Dependence, Drug", "drugs dependence", "drug; dependence", "addictions drugs", "dependence; drug", "dependency drugs", "dependence; drugs", "drugs; dependence", "Dependency (Drug)", "Addiction;drug(s)", "Drug addiction NOS", "addiction to drugs", "ADDICTION ANY DRUG", "Addiction to drugs", "chemical addiction", "Dependence;drug(s)", "Dependence syndrome", "Drug dependence NOS", "chemical dependence", "Chemical dependency", "Chemical Dependence", "Drug dependence, NOS", "Dependent drug abuse", "Drug abuse, dependent", "Dependence drug (NOS)", "DEPENDENCE DRUG (NOS)", "dependence; substance", "Abuse;drug(s);dependent", "Drug addiction syndrome", "Drug dependence syndrome", "drug abuse and dependency", "Drug Dependence Syndromes", "drug dependence (diagnosis)", "Unspecified drug dependence", "Drug dependence, unspecified", "substance abuse drug dependent", "Dependent drug abuse (disorder)", "Other specified drug dependence", "Dependent drug abuse (diagnosis)", "Psychoactive substance dependence", "Psychoactive substance dependence, NOS", "Psychoactive substance dependence (disorder)", "Other specified drug dependence, unspecified", "Other specified drug dependence, unspecified use"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "drug dependence", "shortest_name_length": 14}
{"curie": "UMLS:C1334979", "names": ["Non-Hodgkin Lymphoma by Clinical Course", "Non-Hodgkin's Lymphoma by Clinical Course"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Hodgkin Lymphoma by Clinical Course", "shortest_name_length": 39}
{"curie": "UMLS:C2609259", "names": ["SPD", "Symphysis pubis dysfunction", "Symphysis Pubis Dysfunction", "Pubis Dysfunction, Symphysis", "Dysfunction, Symphysis Pubis", "Symphysis Pubis Dysfunctions", "Pubis Dysfunctions, Symphysis", "Dysfunctions, Symphysis Pubis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Symphysis Pubis Dysfunction", "shortest_name_length": 3}
{"curie": "UMLS:C0001364", "names": ["acute atrophy yellow", "Acute yellow atrophy", "Acute Yellow Atrophy", "acute yellow atrophy", "Atrophy, acute yellow", "Yellow Atrophy, Acute", "Acute hepatic necrosis", "acute hepatic necrosis", "Acute Yellow Atrophies", "hepatic necrosis acute", "Acute necrosis of liver", "acute necrosis of liver", "LIVER, MASSIVE NECROSIS", "massive hepatic necrosis", "Massive hepatic necrosis", "Massive Hepatic Necrosis", "Hepatic Necrosis, Massive", "Massive necrosis of liver", "HEPATIC NECROSIS, MASSIVE", "Acute yellow liver atrophy", "ATROPHY ACUTE YELLOW LIVER", "LIVER, ACUTE YELLOW ATROPHY", "Acute Yellow Atrophy of Liver", "Acute yellow atrophy of liver", "acute hepatic necrosis (diagnosis)", "Acute necrosis of liver (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Massive Hepatic Necrosis", "shortest_name_length": 20}
{"curie": "UMLS:C0475533", "names": ["anemia; nucleotide metabolic disorder", "anemia; disorder nucleotide metabolism", "anemia; nucleotide metabolism disorder", "metabolic disorder; nucleotide with anemia", "disorder; nucleotide metabolism with anemia", "anemia due to disorders nucleotide metabolism", "Anemia due to Disorder of Nucleotide Metabolism", "Anemia due to disorders of nucleotide metabolism", "Anaemia due to disorders of nucleotide metabolism", "anemia due to disorders nucleotide metabolism (diagnosis)", "Anemia due to disorders of nucleotide metabolism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anemia due to disorders of nucleotide metabolism", "shortest_name_length": 37}
{"curie": "UMLS:C0948168", "names": ["bone marrow toxicity", "Bone marrow toxicity", "bone marrow toxicities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone marrow toxicity", "shortest_name_length": 20}
{"curie": "UMLS:C5419902", "names": ["Gallbladder Soft Tissue Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gallbladder Soft Tissue Neoplasm", "shortest_name_length": 32}
{"curie": "MONDO:0005790", "names": ["HAV", "hep a", "hepatitis", "Hep A, NOS", "Hepatitis A", "HEPATITIS A", "a hepatitis", "hepatitis A", "hepatitis a", "hepatitis viral", "hepatitis type A", "Viral hepatitis A", "Acute Hepatitis A", "viral hepatitis A", "hepatitis, A virus", "epidemic; hepatitis", "hepatitis; epidemic", "Hepatitis infectious", "Hepatitis;infectious", "infectious hepatitis", "HEPATITIS INFECTIOUS", "Infectious Hepatitis", "Infectious hepatitis", "Hepatitis A infection", "Hepatitis, Infectious", "hepatitis A infection", "infectious; hepatitis", "HEPATITIS, INFECTIOUS", "Hepatitis A Infection", "hepatitis; infectious", "Infectious Hepatitides", "infectious hepatitis a", "viral hepatitis, type A", "Viral hepatitis, type A", "Hepatitides, Infectious", "Hepatitis infectious NOS", "hepatitis; virus, type, A", "IH - Infectious hepatitis", "virus; hepatitis, type, A", "Infectious Viral Hepatitis", "hepatitis A viral infection", "hepatitis A virus infection", "hepatitis A infection (diagnosis)", "infectious hepatitis (hepatitis A)", "Viral hepatitis, type A (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatitis A virus infection", "shortest_name_length": 3}
{"curie": "MONDO:0005099", "names": ["Subarachnoid bleeding", "subarachnoid hemorrhage", "HEMORRHAGE SUBARACHNOID", "Subarachnoid Hemorrhage", "Subarachnoid hemorrhage", "hemorrhage subarachnoid", "Hemorrhage subarachnoid", "SUBARACHNOID HEMORRHAGE", "subarachnoid haemorrhage", "Hemorrhage, Subarachnoid", "Subarachnoid haemorrhage", "SUBARACHNOID HAEMORRHAGE", "Haemorrhage;subarachnoid", "Haemorrhage subarachnoid", "Subarachnoid Hemorrhages", "hemorrhage; subarachnoid", "subarachnoid hemorrhages", "Hemorrhages, Subarachnoid", "Subarachnoid hemorrhage NOS", "Subarachnoid haemorrhage NOS", "SAH (Subarachnoid Hemorrhage)", "SAH - Subarachnoid hemorrhage", "SAHs (Subarachnoid Hemorrhage)", "SAH - Subarachnoid haemorrhage", "meningeal subarachnoid hemorrhage", "subarachnoid hemorrhage (disease)", "subarachnoid hemorrhage (diagnosis)", "Subarachnoid hemorrhage, unspecified", "Subarachnoid intracranial hemorrhage", "Subarachnoid haemorrhage, unspecified", "Subarachnoid intracranial haemorrhage", "meningeal subarachnoid hemorrhage (diagnosis)", "Subarachnoid intracranial hemorrhage (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subarachnoid hemorrhage", "shortest_name_length": 21}
{"curie": "MONDO:0009489", "names": ["PPKNR", "PPK, Gamborg-Nielsen type", "palmoplantar keratoderma, Norrbotten recessive type", "PALMOPLANTAR KERATODERMA, NORRBOTTEN RECESSIVE TYPE", "Keratoderma, Palmoplantar, Norrbotten Recessive Type", "Hereditary palmoplantar keratoderma Gamborg Nielsen type", "Hereditary palmoplantar keratoderma, Gamborg-Nielsen type", "hereditary palmoplantar keratoderma, Gamborg-Nielsen type", "hereditary palmoplantar hyperkeratosis, Gamborg-Nielsen type", "Hereditary palmoplantar hyperkeratosis, Gamborg-Nielsen type", "Hereditary palmoplantar keratoderma Gamborg Nielsen type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary palmoplantar keratoderma, Gamborg-Nielsen type", "shortest_name_length": 5}
{"curie": "MONDO:0013102", "names": ["BCC3", "basal cell carcinoma, susceptibility to, 3", "BASAL CELL CARCINOMA, SUSCEPTIBILITY TO, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "basal cell carcinoma, susceptibility to, 3", "shortest_name_length": 4}
{"curie": "UMLS:C0018571", "names": ["wound; hand", "Hand injury", "HAND INJURY", "hand injury", "hand; wound", "Hand Injury", "Injury;hand", "hand; injury", "injury; hand", "Injury, Hand", "wound of hand", "Hand Injuries", "hand injuries", "Injuries, Hand", "injury of hand", "Injury of hand", "Injury to hand NOS", "Injury of hand (disorder)", "injury of hand (diagnosis)", "wound of hand (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hand Injuries", "shortest_name_length": 11}
{"curie": "MONDO:0100491", "names": ["GPP", "Von Zumbusch", "generalized pustular psoriasis", "generalized psoriasis pustular", "Generalized pustular psoriasis", "psoriasis generalized pustular", "Generalised pustular psoriasis", "Pustular psoriasis, generalized", "Acute generalised pustular psoriasis", "Acute generalized pustular psoriasis", "Generalized pustular psoriasis (disorder)", "generalized pustular psoriasis (diagnosis)", "Generalized pustular psoriasis of von Zumbush", "Pustular psoriasis, generalized, von Zumbusch", "Generalized pustular psoriasis of von Zumbusch", "Generalised pustular psoriasis of von Zumbusch"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "generalized pustular psoriasis", "shortest_name_length": 3}
{"curie": "MONDO:0017111", "names": ["isolated Dandy-Walker malformation without hydrocephalus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated Dandy-Walker malformation without hydrocephalus", "shortest_name_length": 56}
{"curie": "MONDO:0003085", "names": ["keratitis", "Keratitis", "KERATITIS", "Keratitides", "Keratitis NOS", "Keratitis, NOS", "Cornea inflamed", "Keratitis;measles", "Corneal keratitis", "cornea inflammation", "cornea; inflammation", "CORNEAL INFLAMMATION", "corneal inflammation", "Corneal inflammation", "INFLAMMATION CORNEAL", "inflammation; cornea", "Keratitis (disorder)", "Inflammation corneal", "keratitis (diagnosis)", "Unspecified keratitis", "Inflammation of cornea", "Keratitis, unspecified", "inflammation of cornea", "keratitis (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratitis", "shortest_name_length": 9}
{"curie": "MONDO:0014803", "names": ["SPAHGC", "spasticity-ataxia-gait anomalies syndrome", "Spasticity-ataxia-gait anomalies syndrome", "Spasticity, ataxia, gait anomalies syndrome", "childhood-onset spasticity with hyperglycinemia", "Childhood-onset spasticity with hyperglycinemia", "Childhood-onset spasticity with hyperglycinaemia", "spasticity, childhood-onset, with hyperglycinemia", "SPASTICITY, CHILDHOOD-ONSET, WITH HYPERGLYCINEMIA", "Childhood-onset spasticity with hyperglycinemia (disorder)", "childhood-onset spasticity with variant non-ketotic hyperglycinemia", "Childhood-onset spasticity with variant non-ketotic hyperglycinemia", "Childhood-onset spasticity with variant non-ketotic hyperglycinaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spasticity-ataxia-gait anomalies syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C2981663", "names": ["Stage 0 Distal Bile Duct Cancer", "stage 0 distal bile duct cancer", "Stage 0 Distal Bile Duct Cancer AJCC v7", "stage 0 distal extrahepatic bile duct cancer", "Stage 0 Extrahepatic (Distal) Bile Duct Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Distal Bile Duct Cancer AJCC v7", "shortest_name_length": 31}
{"curie": "UMLS:C0232591", "names": ["Vagotonia", "vagotonia", "Gastric hypertonus", "Gastric tone increased", "Increased gastric tonus", "Stomach tonus increased", "Gastric tonus, increased", "Increased gastric tonus (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Increased gastric tonus", "shortest_name_length": 9}
{"curie": "UMLS:C1266024", "names": ["Flat Adenoma", "Flat adenoma", "GI Tract Flat Adenoma", "Gastrointestinal Tract Flat Adenoma", "Flat adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Flat adenoma", "shortest_name_length": 12}
{"curie": "MONDO:0009978", "names": ["MacKay Shek Carr syndrome", "Mackay Shek Carr syndrome", "Mackay-Shek-Carr syndrome", "Retinal degeneration, nanophthalmos, glaucoma", "retinal degeneration, nanophthalmos, glaucoma", "Retinal degeneration-nanophthalmos-glaucoma syndrome", "retinal degeneration-nanophthalmos-glaucoma syndrome", "Retinal degeneration, nanophthalmos, glaucoma syndrome", "Retinal degeneration, nanophthalmos, glaucoma syndrome (disorder)", "retinal degeneration with nanophthalmos, cystic macular degeneration, and angle closure glaucoma", "RETINAL DEGENERATION WITH NANOPHTHALMOS, CYSTIC MACULAR DEGENERATION, AND ANGLE CLOSURE GLAUCOMA", "Retinal Degeneration with Nanophthalmos, Cystic Macular Degeneration, and Angle Closure Glaucoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal degeneration-nanophthalmos-glaucoma syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0035764", "names": ["Secondary SRNS", "Secondary steroid-resistant nephrotic syndrome", "Idiopathic SSNS with secondary steroid resistance", "idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance", "shortest_name_length": 14}
{"curie": "MONDO:0000744", "names": ["Lung Abscess", "LUNG ABSCESS", "Abscess;lung", "lung abscess", "Lung abscess", "abscess lung", "abscess lungs", "Abscess, Lung", "lung; abscess", "abscess; lung", "LUNG, ABSCESS", "Lungs--Abscess", "lung abscesses", "abscesses lung", "Lung Abscesses", "Abscesses, Lung", "Abscess of lung", "of lung abscess", "abscess of lung", "Lung abscess NOS", "pulmonary abscess", "PULMONARY ABSCESS", "Pulmonary Abscess", "abscess pulmonary", "Pulmonary abscess", "Abscess, Pulmonary", "pulmonary abscesses", "Abscess of lung NOS", "Pulmonary Abscesses", "Abscesses, Pulmonary", "lung abscess (disease)", "lung abscess (diagnosis)", "Abscess of lung (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung abscess", "shortest_name_length": 12}
{"curie": "UMLS:C0233681", "names": ["Grandiosity", "grandiosity", "DELUSION GRANDEUR", "grandiose delusion", "Grandiose delusion", "Grandiose delusions", "grandiose delusions", "delusions grandiose", "delusion of grandeur", "Self esteem inflated", "Inflated self-esteem", "Delusion of grandeur", "inflated self-esteem", "Delusions Of Grandeur", "delusions of grandeur", "Delusions of grandeur", "Inflated self-opinion", "Grandiose delusions (finding)", "inflated self-esteem (symptom)", "Inflated self-opinion (finding)", "grandiose delusions (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grandiose delusions", "shortest_name_length": 11}
{"curie": "UMLS:C5205607", "names": ["Advanced Paraganglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Paraganglioma", "shortest_name_length": 22}
{"curie": "UMLS:C0158698", "names": ["URINARY TRACT ANOMALY", "anomaly; urinary tract", "urinary tract; anomaly", "deformity; urinary tract", "urinary tract; deformity", "Urinary tract malformation", "URINARY TRACT MALFORMATION", "Congenital Urinary Anomaly", "urinary tract malformation", "Urinary tract malformation NOS", "Congenital anomaly urinary tract", "Congenital anomalies urinary tract", "Congenital Anomaly of Urinary Tract", "Urinary system congenital anomalies", "Congenital urinary tract anomaly NOS", "Congenital Urinary System Abnormality", "Unspecified anomaly of urinary system", "congenital anomalies of urinary system", "Congenital anomalies of urinary system", "Congenital anomaly of the urinary tract", "Congenital anomaly NOS of urinary system", "Congenital anomaly of the urinary system", "Congenital anomaly of urinary tract, NOS", "Congenital abnormality of urinary system", "Congenital deformity of the urinary tract", "Congenital deformity NOS of urinary system", "congenital anomaly of urinary tract proper", "CONGENITAL ANOMALIES OF THE URINARY SYSTEM", "Congenital deformity of urinary tract, NOS", "Congenital Abnormality of the Urinary System", "Congenital malformation of the urinary system", "Congenital anomaly of the urinary system, NOS", "Congenital anomaly of the urinary tract proper", "Congenital malformations of the urinary system", "Unspecified congenital anomaly of urinary system", "congenital anomalies of urinary system (diagnosis)", "congenital anomaly of urinary tract proper (diagnosis)", "Congenital malformation of urinary system, unspecified", "Congenital malformation of the urinary system (disorder)", "Congenital malformations of the urinary system (Q60-Q64)", "Congenital anomaly of the urinary tract proper (disorder)", "CONGENITAL ANOMALIES OF THE URINARY SYSTEM: GENERAL TERMS", "Congenital anomaly NOS of urinary system any part, except urachus", "Congenital deformity NOS of urinary system any part, except urachus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital anomaly of the urinary tract proper", "shortest_name_length": 21}
{"curie": "MONDO:0002525", "names": ["fat disorder", "FAT DISORDER", "dyslipidemia", "disorders fat", "Lipid disorder", "lipid disorder", "disorders fats", "disorders lipid", "lipid disorders", "Lipid Disorders", "disorders lipids", "Disease;lipid metabolism", "lipid metabolism disease", "lipid; metabolic disorder", "lipid metabolism disorder", "Disorder;lipid metabolism", "Lipid Metabolism Disorder", "disorder lipid metabolism", "metabolic disorder; lipid", "Lipid metabolism disorder", "lipid metabolism disorders", "disorder; lipid metabolism", "Metabolism Disorder, Lipid", "lipoid metabolism disorder", "Lipid Metabolism Disorders", "Lipid metabolism disorders", "Disease of lipid metabolism", "Metabolism Disorders, Lipid", "Disorder of Lipid Metabolism", "Disorder of lipid metabolism", "disorder of lipid metabolism", "Lipid metabolism disorder NOS", "Disorders of lipid metabolism", "Lipids--Metabolism--Disorders", "disorders of lipid metabolism", "LIPID METABOLISM DISORDER NOS", "fatty acid metabolism disorder", "Lipid Metabolism, Inborn Error", "Disorders of lipoid metabolism", "Lipid Metabolism, Inborn Errors", "Inborn error of lipid metabolism", "Inborn errors of lipid metabolism", "inherited lipid metabolism disorder", "lipoid metabolism disorder (diagnosis)", "Disorder of lipid metabolism (disorder)", "Unspecified disorder of lipoid metabolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited lipid metabolism disorder", "shortest_name_length": 12}
{"curie": "MONDO:0002093", "names": ["acanthoma", "Acanthoma", "Acanthomas", "acanthoma (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acanthoma", "shortest_name_length": 9}
{"curie": "UMLS:C0948692", "names": ["necrotizing colitis", "Necrotizing colitis", "Necrotising colitis", "necrotising colitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Necrotizing colitis", "shortest_name_length": 19}
{"curie": "UMLS:C0578736", "names": ["Groin lymphadenopathy", "inguinal lymphadenopathy", "Lymphadenopathy inguinal", "INGUINAL LYMPHADENOPATHY", "Inguinal lymphadenopathy", "enlarged inguinal lymph node", "inguinal lymph nodes enlarged", "Inguinal lymph nodes enlarged", "INGUINAL LYMPH NODE ENLARGEMENT", "inguinal lymph node enlargement", "Enlargement of inguinal lymph node", "Inguinal lymphadenopathy (disorder)", "enlarged inguinal lymph node (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Inguinal lymphadenopathy", "shortest_name_length": 21}
{"curie": "UMLS:C0861216", "names": ["Stage I Centroblastic Lymphoma", "Centroblastic lymphoma stage I", "Ann Arbor Stage I Centroblastic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Centroblastic lymphoma stage I", "shortest_name_length": 30}
{"curie": "MONDO:0007764", "names": ["VBCH2", "Worth disease", "Worth syndrome", "Worth's syndrome", "Endosteal hyperostosis", "hyperostosis, endosteal", "Worth disease (disorder)", "Van Buchem disease type 2", "Van Buchem disease, type 2", "autosomal dominant osteosclerosis", "Autosomal dominant osteosclerosis", "Endosteal hyperostosis Worth type", "OSTEOSCLEROSIS, AUTOSOMAL DOMINANT", "Osteosclerosis, Autosomal Dominant", "Endosteal hyperostosis, Worth type", "osteosclerosis, autosomal dominant", "endosteal hyperostosis, Worth type", "autosomal dominant endosteal hyperostosis", "Endosteal Hyperostosis, Autosomal Dominant", "ENDOSTEAL HYPEROSTOSIS, AUTOSOMAL DOMINANT", "endosteal hyperostosis, autosomal dominant", "Benign hyperostosis corticalis generalisata", "Autosomal dominant osteosclerosis, Worth type", "autosomal dominant osteosclerosis, Worth type", "Ostéosclérose autosomique dominante type Worth", "osteosclerosis, autosomal dominant, Worth type", "Hyperostosis corticalis generalisata congenita", "osteosclerosis of the skull and enlarged mandible", "Osteosclerosis, autosomal dominant Worth type with torus palatinus", "benign form of Worth hyperostosis corticalis generalisata with torus platinus", "hyperostosis corticalis generalisata, benign form of Worth with torus palatinus", "hyperostosis corticalis generalisata, benign form of Worth, with torus palatinus", "Hyperostosis Corticalis Generalisata, Benign Form Of Worth, With Torus Palatinus", "HYPEROSTOSIS CORTICALIS GENERALISATA, BENIGN FORM OF WORTH, WITH TORUS PALATINUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant osteosclerosis, Worth type", "shortest_name_length": 5}
{"curie": "MONDO:0008504", "names": ["SVAS", "Supra-aortic stenosis", "supravalvar aortic stenosis", "Supravalvar Aortic Stenosis", "Supravalvar aortic stenosis", "aortic stenosis supravalvar", "Aortic Supravalvular Stenosis", "SUPRAVALVULAR AORTIC STENOSIS", "Supravalvular aortic stenosis", "Supravalvular Aortic Stenosis", "supravalvular aortic stenosis", "aortic supravalvular stenosis", "Aortic Supravalvular Stenoses", "Stenosis, Supravalvular Aortic", "Supravalvular Stenoses, Aortic", "Supravalvular Stenosis, Aortic", "Stenoses, Aortic Supravalvular", "supra-valvular aortic stenosis", "Aortic Stenosis, Supravalvular", "Supra-valvular aortic stenosis", "aortic stenosis supra valvular", "Stenosis, Aortic Supravalvular", "Supravalvular aorta constricted", "SVAS - Supravalvar aortic stenosis", "Supravalvar aortic stenosis (disorder)", "supravalvular aortic stenosis (disease)", "Supravalvar aortic stenosis (diagnosis)", "Supravalvar aortic stenosis, eisenberg type", "supravalvar aortic stenosis, Eisenberg type", "SUPRAVALVAR AORTIC STENOSIS, EISENBERG TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "supravalvular aortic stenosis", "shortest_name_length": 4}
{"curie": "MONDO:0003638", "names": ["lung meningioma", "Lung Meningioma", "Meningioma of Lung", "meningioma of lung", "pulmonary meningioma", "Pulmonary Meningioma", "meningioma of the lung", "Meningioma of the Lung", "lung primary meningioma", "Primary Lung Meningioma", "lung meningioma (disease)", "Primary Meningioma of Lung", "meningioma (disease) of lung", "Primary Pulmonary Meningioma", "primary pulmonary meningioma", "Primary Meningioma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung meningioma", "shortest_name_length": 15}
{"curie": "MONDO:0014302", "names": ["SPG62", "hereditary spastic paraplegia 62", "hereditary spastic paraplegia type 62", "autosomal recessive spastic paraplegia 62", "SPASTIC PARAPLEGIA 62, AUTOSOMAL RECESSIVE", "spastic paraplegia 62, autosomal recessive", "Autosomal recessive spastic paraplegia type 62", "autosomal recessive spastic paraplegia type 62", "ERLIN1 autosomal recessive pure spastic paraplegia", "familial spastic paraplegia autosomal recessive type 62", "Autosomal recessive spastic paraplegia type 62 (disorder)", "Autosomal recessive spastic paraplegia type 62 (diagnosis)", "autosomal recessive pure spastic paraplegia caused by mutation in ERLIN1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 62", "shortest_name_length": 5}
{"curie": "MONDO:0002670", "names": ["ampullary adenocarcinoma", "Ampullary Adenocarcinoma", "Ampulla of Vater Adenocarcinoma", "ampulla of Vater adenocarcinoma", "ampulla of vater adenocarcinoma", "adenocarcinoma of ampulla of vater", "Adenocarcinoma of ampulla of Vater", "Adenocarcinoma of Ampulla of Vater", "adenocarcinoma of ampulla of Vater", "hepatopancreatic ampulla adenocarcinoma", "Invasive Adenocarcinoma of the Ampullary Region", "invasive adenocarcinoma of the ampullary region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ampulla of vater adenocarcinoma", "shortest_name_length": 24}
{"curie": "UMLS:C4525140", "names": ["Stage IIIC Rectal Cancer", "stage IIIC rectal cancer", "Stage IIIC Rectal Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Rectal Cancer AJCC v8", "shortest_name_length": 24}
{"curie": "UMLS:C2827412", "names": ["Distant Intracranial Metastasis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Distant Intracranial Metastasis", "shortest_name_length": 31}
{"curie": "MONDO:0001938", "names": ["vulva dystrophy", "dystrophy vulva", "dystrophy; vulva", "vulvar dystrophy", "dystrophy vulvar", "vulva; dystrophy", "Vulvar Dystrophy", "dystrophy of vulva", "dystrophies vulvar", "Dystrophy of vulva", "Dystrophy of vulva (disorder)", "dystrophy of vulva (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar dystrophy", "shortest_name_length": 15}
{"curie": "MONDO:0012394", "names": ["SYNS2", "multiple synostoses syndrome 2", "Multiple synostoses syndrome 2", "MULTIPLE SYNOSTOSES SYNDROME 2", "GDF5 multiple synostoses syndrome", "multiple synostoses syndrome type 2", "multiple synostoses syndrome caused by mutation in GDF5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple synostoses syndrome 2", "shortest_name_length": 5}
{"curie": "MONDO:0017949", "names": ["HCHWA, Arctic type", "ABetaE22G amyloidosis", "ABeta amyloidosis, Arctic type", "cerebral amyloid angiopathy, APP-related, Arctic variant", "hereditary cerebral hemorrhage with amyloidosis, Arctic type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ABeta amyloidosis, Arctic type", "shortest_name_length": 18}
{"curie": "UMLS:C4764279", "names": ["Unresectable Ureter Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Ureter Urothelial Carcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0013163", "names": ["NPHPL1", "NPHP-XPNPEP3", "XPNPEP3 nephronophthisis (disease)", "NEPHRONOPHTHISIS-LIKE NEPHROPATHY 1", "nephronophthisis-like nephropathy 1", "nephronophthisis-like nephropathy type 1", "nephronophthisis (disease) caused by mutation in XPNPEP3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephronophthisis-like nephropathy 1", "shortest_name_length": 6}
{"curie": "MONDO:0018337", "names": ["severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency", "shortest_name_length": 68}
{"curie": "MONDO:0010020", "names": ["CGL2", "Seip syndrome", "Seip Syndrome", "SEIP SYNDROME", "Syndrome, Seip", "Brunzell Syndrome", "Syndrome, Brunzell", "Berardinelli Syndrome", "Berardinelli syndrome", "BERARDINELLI SYNDROME", "Syndrome, Berardinelli", "Berardinelli-Seip syndrome", "Brunzell syndrome BSCL2-related", "BSCL2-related Brunzell syndrome", "Congenital Lipoatrophic Diabete", "BSCL2-Related Brunzell Syndrome", "Brunzell Syndrome, BSCL2 Related", "Congenital Lipoatrophic Diabetes", "Brunzell syndrome, BSCL2-related", "Brunzell Syndrome, BSCL2-Related", "Lipoatrophic Diabete, Congenital", "Syndrome, BSCL2-Related Brunzell", "BRUNZELL SYNDROME, BSCL2-RELATED", "Diabete, Congenital Lipoatrophic", "congenital lipoatrophic diabetes", "Diabetes, Congenital Lipoatrophic", "Lipoatrophic Diabetes, Congenital", "LIPOATROPHIC DIABETES, CONGENITAL", "lipoatrophic diabetes, congenital", "Congenital Generalized Lipodystrophy Type 2", "congenital generalized lipodystrophy type 2", "lipodystrophy, congenital generalized, type 2", "Lipodystrophy, Congenital Generalized, Type 2", "LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2", "Total Lipodystrophy and Acromegaloid Gigantism", "total lipodystrophy and acromegaloid gigantism", "lipodystrophy, total, and acromegaloid gigantism", "Lipodystrophy, Total, And Acromegaloid Gigantism", "LIPODYSTROPHY, TOTAL, AND ACROMEGALOID GIGANTISM", "Berardinelli-Seip Congenital Lipodystrophy Type 2", "Berardinelli Seip Congenital Lipodystrophy Type 2", "Berardinelli-Seip congenital lipodystrophy type 2", "Berardinelli Seip congenital lipodystrophy type 2", "Berardinelli-Seip Congenital Lipodystrophy, Type 2", "BERARDINELLI-SEIP CONGENITAL LIPODYSTROPHY, TYPE 2", "Berardinelli Seip Congenital Lipodystrophy, Type 2", "Berardinelli-Seip congenital lipodystrophy, type 2", "LIPODYSTROPHY, BERARDINELLI-SEIP CONGENITAL, TYPE 2", "lipodystrophy, Berardinelli-Seip congenital, type 2", "Lipodystrophy, Berardinelli-Seip Congenital, Type 2", "BSCL2 congenital generalized lipodystrophy (disease)", "congenital generalized lipodystrophy (disease) caused by mutation in BSCL2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital generalized lipodystrophy type 2", "shortest_name_length": 4}
{"curie": "MONDO:0006829", "names": ["LEUKEMOID REACTION", "Leukemoid reaction", "REACTION LEUKEMOID", "leukemoid reaction", "Reaction leukemoid", "Leukemoid Reaction", "Leukaemoid reaction", "LEUKAEMOID REACTION", "leukemoid reactions", "leukemoid; reaction", "Leukemoid Reactions", "Reaction, Leukemoid", "reaction; leukemoid", "Leukemoid reactions", "Reactions, Leukemoid", "Leukemoid reaction NOS", "Leukemoid reaction, NOS", "Leukemoid reaction (disorder)", "leukemoid reaction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukemoid reaction", "shortest_name_length": 18}
{"curie": "MONDO:0023657", "names": ["MRD65", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 65", "mental retardation, autosomal dominant 65", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 65", "intellectual developmental disorder, autosomal dominant 65"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder, autosomal dominant 65", "shortest_name_length": 5}
{"curie": "MONDO:0003202", "names": ["basophil carcinoma", "Basophil carcinoma", "Basophil Carcinoma", "Basophilic Carcinoma", "basophilic carcinoma", "Basophil Adenocarcinoma", "Basophil adenocarcinoma", "basophil adenocarcinoma", "Basophilic Adenocarcinoma", "basophilic adenocarcinoma", "Mucoid cell adenocarcinoma", "pituitary gland basophil carcinoma", "Pituitary Gland Basophil Carcinoma", "pituitary gland basophilic carcinoma", "basophil carcinoma of pituitary gland", "Basophil carcinoma (morphologic abnormality)", "basophil carcinoma (morphologic abnormality)", "basophil carcinoma of pituitary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pituitary gland basophilic carcinoma", "shortest_name_length": 18}
{"curie": "MONDO:0010280", "names": ["PTOSX", "PTOS2", "Ptos2", "ptosis, X-linked", "PTOSIS, X-LINKED", "Ptosis, X-Linked", "Ptosis, Hereditary Congenital 2", "ptosis, hereditary congenital 2", "PTOSIS, HEREDITARY CONGENITAL 2", "ptosis, hereditary congenital type 2", "ptosis, hereditary congenital 2, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ptosis, hereditary congenital 2", "shortest_name_length": 5}
{"curie": "MONDO:0009566", "names": ["Marfanoid mental retardation syndrome autosomal", "MARFANOID mental retardation syndrome, autosomal", "Marfanoid Mental Retardation Syndrome, Autosomal", "MARFANOID MENTAL RETARDATION SYNDROME, AUTOSOMAL", "Marfanoid intellectual disability syndrome autosomal", "MARFANOID intellectual disability syndrome, autosomal", "marfanoid habitus-autosomal recessive intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "marfanoid habitus-autosomal recessive intellectual disability syndrome", "shortest_name_length": 47}
{"curie": "MONDO:0005917", "names": ["Placenta Disease", "placenta disease", "placental disease", "disease, placenta", "placenta disorder", "Disease, Placenta", "Placenta Disorder", "placenta diseases", "Placental Disease", "Placenta Diseases", "Placental Diseases", "Placenta--Diseases", "placenta; disorder", "disease, placental", "disorder, placenta", "placental diseases", "diseases, placenta", "DISORDER PLACENTAL", "Diseases, Placenta", "placental disorder", "Disease, Placental", "Disorder, Placenta", "placenta disorders", "Placenta Disorders", "PLACENTAL DISORDER", "Disorder placental", "Placental Disorder", "Placental disorder", "disease of placenta", "Disorders, Placenta", "disorders, placenta", "diseases, placental", "Placental disorders", "placental disorders", "Diseases, Placental", "Disorder of placenta", "disorder of placenta", "Placental disorder NOS", "placenta disease or disorder", "pregnancy; disease, placenta", "pregnancy; placenta, disease", "Unspecified placental disorder", "disease or disorder of placenta", "Disorder of placenta (disorder)", "Placental disorder, unspecified", "disease (or disorder); placenta", "placental disorders (diagnosis)", "Non-Neoplastic Placenta Disorder", "Placental Non-Neoplastic Disease", "Placental Non-Neoplastic Disorder", "Disorder of placenta and placental transfusion", "Unspecified placental disorder, unspecified trimester"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "placenta disorder", "shortest_name_length": 16}
{"curie": "UMLS:C5418885", "names": ["Metastatic Uterine Corpus Carcinosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Uterine Corpus Carcinosarcoma", "shortest_name_length": 40}
{"curie": "MONDO:0009308", "names": ["CGD4", "Cyba deficiency", "CYBA DEFICIENCY", "CYBA deficiency", "CYBA Deficiency", "autosomal recessive cytochrome b-negative CGD", "CGD, AUTOSOMAL RECESSIVE CYTOCHROME b-NEGATIVE", "CGD, autosomal recessive cytochrome B-negative", "autosomal recessive chronic granulomatous disease 4", "chronic granulomatous disease 4, autosomal recessive", "GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, 4", "chronic granulomatous disease due to deficiency of CYBA", "CGD DUE TO DEFICIENCY OF THE ALPHA SUBUNIT OF CYTOCHROME b", "CGD due to deficiency of the alpha subunit of cytochrome b", "CGD due to deficiency of the Alpha Subunit of cytochrome B", "autosomal recessive chronic granulomatous disease cytochrome b-negative", "Chronic Granulomatous Disease, Autosomal Recessive Cytochrome B-Negative", "granulomatous disease, chronic, autosomal recessive, cytochrome b-negative", "Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative", "GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE", "Chronic Granulomatous Disease due to Deficiency of the Alpha Subunit of Cytochrome B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "granulomatous disease, chronic, autosomal recessive, cytochrome b-negative", "shortest_name_length": 4}
{"curie": "MONDO:0010963", "names": ["DFNA6", "DFNA14", "DFNA38", "autosomal dominant deafness 6", "autosomal dominant deafness 14", "Deafness, Autosomal Dominant 6", "DEAFNESS, AUTOSOMAL DOMINANT 6", "deafness, autosomal dominant 6", "autosomal dominant deafness 38", "deafness, autosomal dominant 14", "DEAFNESS, AUTOSOMAL DOMINANT 14", "DEAFNESS, AUTOSOMAL DOMINANT 38", "Deafness, Autosomal Dominant 38", "deafness, autosomal dominant 38", "Deafness, Autosomal Dominant 14", "deafness, autosomal dominant type 6", "deafness, autosomal dominant 6/14/38", "autosomal dominant nonsyndromic deafness 6", "WFS1 autosomal dominant nonsyndromic deafness", "autosomal dominant nonsyndromic hearing loss 6", "autosomal dominant nonsyndromic deafness type 6", "autosomal dominant nonsyndromic deafness caused by mutation in WFS1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 6", "shortest_name_length": 5}
{"curie": "MONDO:0006702", "names": ["CIDP", "cidp", "chronic relapsing polyneuropathy", "Chronic Inflammatory Polyradiculopathy", "Polyradiculopathy, Chronic Inflammatory", "Inflammatory Polyradiculopathy, Chronic", "Chronic Inflammatory Polyradiculopathies", "Inflammatory Polyradiculopathies, Chronic", "Polyradiculopathies, Chronic Inflammatory", "Chronic Inflammatory Polyradiculoneuropathy", "Inflammatory Polyradiculoneuropathy, Chronic", "Polyradiculoneuropathy, Chronic Inflammatory", "Chronic Inflammatory Polyradiculoneuropathies", "Polyradiculoneuropathies, Chronic Inflammatory", "Inflammatory Polyradiculoneuropathies, Chronic", "Chronic inflammatory demyelinating polyneuritis", "Chronic Inflammatory Demyelinating Polyneuritis", "Chronic inflammatory demyelinating polyneuropathy", "Chronic Inflammatory Demyelinating Polyneuropathy", "chronic inflammatory demyelinating polyneuropathy", "Polyneuropathy, Inflammatory Demyelinating, Chronic", "POLYNEUROPATHY, INFLAMMATORY DEMYELINATING, CHRONIC", "CIDP - Chronic inflammatory demyelinating polyneuropathy", "Chronic inflammatory demyelinating polyradiculoneuropathy", "CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY", "chronic inflammatory demyelinating polyradiculoneuropathy", "Chronic Inflammatory Demyelinating Polyradiculoneuropathy", "Polyradiculoneuropathy, Chronic Inflammatory Demyelinating", "chronic inflammatory demyelinating polyneuropathy (diagnosis)", "CIDP - Chronic inflammatory demyelinating polyradiculoneuropathy", "chronic inflammatory demyelinating polyradiculoneuropathy (CIDP)", "Chronic inflammatory demyelinating polyradiculoneuropathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic inflammatory demyelinating polyradiculoneuropathy", "shortest_name_length": 4}
{"curie": "MONDO:0005990", "names": ["tracheitis", "Tracheitis", "TRACHEITIS", "Tracheitides", "Tracheitis NOS", "Tracheitis, NOS", "acute tracheitis", "Acute tracheitis", "Tracheitis;acute", "Inflamed trachea", "TRACHEITIS ACUTE", "TRACHEITIS, ACUTE", "Chronic tracheitis", "Tracheitis;chronic", "chronic tracheitis", "chronic; tracheitis", "tracheitis; chronic", "Acute tracheitis, NOS", "Tracheitis (disorder)", "tracheal Inflammation", "Tracheal Inflammation", "Tracheal inflammation", "tracheitis (diagnosis)", "Tracheitis (acute) NOS", "Acute tracheitis (disorder)", "tracheal mucosa inflammation", "acute tracheitis (diagnosis)", "Chronic tracheitis (disorder)", "chronic tracheitis (diagnosis)", "inflammation of tracheal mucosa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tracheitis", "shortest_name_length": 10}
{"curie": "MONDO:0006210", "names": ["FLC", "FHCC", "FL-HCC", "Fibrolamellar Cancer", "fibrolamellar cancer", "fibrolamellar carcinoma", "Fibrolamellar Carcinoma", "Fibrolamellar hepatocarcinoma", "fibrolamellar hepatocarcinoma", "Oncocytic Hepatocellular tumor", "oncocytic hepatocellular tumor", "Oncocytic Hepatocellular Tumor", "fibrolamellar oncocytic hepatoma", "eosinophilic glassy cell hepatoma", "liver cell fibrolamellar carcinoma", "Liver Cell Fibrolamellar Carcinoma", "Fibrolamellar hepatocellular carcinoma", "fibrolamellar carcinoma of liver cells", "fibrolamellar hepatocellular carcinoma", "Hepatocellular Fibrolamellar Carcinoma", "Fibrolamellar Hepatocellular Carcinoma", "Fibrolamellar Carcinoma of Liver Cells", "hepatocellular fibrolamellar carcinoma", "hepatocellular carcinoma, fibrolamellar", "Hepatocellular carcinoma, fibrolamellar", "fibrolamellar; hepatocellular carcinoma", "carcinoma; hepatocellular, fibrolamellar", "hepatocellular; carcinoma, fibrolamellar", "Fibrolamellar Carcinoma of the Liver Cells", "fibrolamellar carcinoma of the liver cells", "fibrolamellar hepatocellular carcinoma of liver", "Hepatocellular carcinoma (fibrolamellar variant)", "hepatocellular carcinoma (fibrolamellar variant)", "fibrolamellar variant of hepatocellular carcinoma", "Fibrolamellar hepatocellular carcinoma (disorder)", "Fibrolamellar variant of hepatocellular carcinoma", "hepatocellular carcinoma with increased stromal fibrosis", "fibrolamellar hepatocellular carcinoma of liver (diagnosis)", "polygonal cell hepatocellular carcinoma with fibrous stroma", "eosinophilic hepatocellular carcinoma with lamellar fibrosis", "polygonal cell type hepatocellular carcinoma with fibrous Stroma", "Polygonal Cell Type Hepatocellular Carcinoma with Fibrous Stroma", "Hepatocellular carcinoma, fibrolamellar (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibrolamellar hepatocellular carcinoma", "shortest_name_length": 3}
{"curie": "MONDO:0044311", "names": ["BTDD", "MCINS", "MACINNES SYNDROME", "Macinnes syndrome", "BRACHYCEPHALY, TRICHOMEGALY, AND DEVELOPMENTAL DELAY", "brachycephaly, trichomegaly, and developmental delay"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachycephaly, trichomegaly, and developmental delay", "shortest_name_length": 4}
{"curie": "UMLS:C0852875", "names": ["eye allergy", "Eye allergy", "allergy eye", "allergy eyes", "allergies eye", "allergies eyes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eye allergy", "shortest_name_length": 11}
{"curie": "UMLS:C5205709", "names": ["Sinonasal Adenocarcinoma, Intestinal-Type with Mucinous Pattern"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Adenocarcinoma, Intestinal-Type with Mucinous Pattern", "shortest_name_length": 63}
{"curie": "UMLS:C4744564", "names": ["Metastatic Colorectal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Colorectal Carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0018556", "names": ["LEMS", "Myasthenic syndrome", "myasthenic syndrome", "myasthenic syndromes", "Eaton Lambert Syndrome", "Lambert Eaton Syndrome", "Eaton Lambert syndrome", "lambert eaton syndrome", "eaton-lambert syndrome", "Lambert-Eaton Syndrome", "Eaton-Lambert Syndrome", "Lambert-Eaton syndrome", "Eaton-Lambert syndrome", "LAMBERT EATON SYNDROME", "lambert-eaton syndrome", "eaton lambert syndrome", "Lambert Eaton syndrome", "EATON-LAMBERT SYNDROME", "Syndrome, Eaton-Lambert", "Syndrome, Lambert-Eaton", "Lambert-Eaton (etiology)", "Eaton-Lambert (etiology)", "Lambert-Eaton syndrome NOS", "EATON-LAMBERT-ROOKE SYNDROME", "Eaton-Lambert (manifestation)", "Lambert-Eaton (manifestation)", "Lambert-Eaton Myasthenic Syndrome", "Eaton-Lambert syndrome (disorder)", "Lambert-Eaton myasthenic syndrome", "Lambert Eaton myasthenic syndrome", "Lambert Eaton Myasthenic Syndrome", "Eaton-Lambert Myasthenic Syndrome", "Eaton Lambert Myasthenic Syndrome", "Eaton Lambert myasthenic syndrome", "Myasthenic Syndrome, Eaton-Lambert", "Myasthenic Syndrome, Lambert-Eaton", "Lambert-Eaton syndrome (diagnosis)", "Syndrome, Eaton-Lambert Myasthenic", "Myasthenic Syndrome, Lambert Eaton", "Syndrome, Lambert-Eaton Myasthenic", "myasthenic syndrome of Lambert Eaton", "myasthenic syndrome of Lambert-Eaton", "LEMS - Lambert-Eaton myasthenic syndrome", "Lambert-Eaton Myopathic-Myasthenic Syndrome", "Lambert-Eaton Myasthenic-Myopathic Syndrome", "Eaton-Lambert Myasthenic-Myopathic Syndrome", "Eaton-Lambert Myopathic-Myasthenic Syndrome", "Lambert-Eaton Myasthenic-Myopathic Syndromes", "Eaton-Lambert Myopathic-Myasthenic Syndromes", "Lambert-Eaton Myopathic-Myasthenic Syndromes", "Myasthenic Myopathic Syndrome of Eaton Lambert", "Myasthenic-Myopathic Syndrome of Eaton-Lambert", "myasthenic-myopathic syndrome of Lambert-Eaton", "Myasthenic-Myopathic Syndrome of Lambert-Eaton", "Myasthenic Myopathic Syndrome of Lambert Eaton", "Myopathic-Myasthenic Syndrome of Lambert-Eaton", "Myopathic-Myasthenic Syndrome of Eaton-Lambert", "Myopathic Myasthenic Syndrome of Eaton Lambert"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lambert-Eaton myasthenic syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0009558", "names": ["TCS3", "TREACHER COLLINS SYNDROME 3", "Treacher Collins syndrome 3", "TREACHER COLLINS syndrome 3", "Treacher Collins syndrome type 3", "POLR1C Treacher-Collins syndrome", "Treacher-Collins syndrome caused by mutation in POLR1C", "mandibulofacial dysostosis, Treacher Collins type, autosomal recessive", "MANDIBULOFACIAL DYSOSTOSIS, TREACHER COLLINS TYPE, AUTOSOMAL RECESSIVE", "Mandibulofacial dysostosis, Treacher Collins type, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Treacher Collins syndrome 3", "shortest_name_length": 4}
{"curie": "MONDO:0043251", "names": ["odontoma", "Odontoma", "Odontomas", "odontomas", "Odontoma NOS", "Odontoma, NOS", "fibroodontoma", "Fibroodontoma", "fibro-odontoma", "Fibro-Odontoma", "fibroodontomas", "Fibroodontomas", "fibro odontoma", "Fibro Odontoma", "Benign odontoma", "Fibro-Odontomas", "fibro-odontomas", "ODONTOMA, BENIGN", "odontoma, benign", "compound odontoma", "compound odontomas", "odontoma, compound", "odontomas, compound", "odontoma (diagnosis)", "ameloblastic fibro-odontoma", "fibro-odontoma, ameloblastic", "ameloblastic fibro-odontomas", "fibro odontoma, ameloblastic", "fibro-odontomas, ameloblastic", "Benign odontoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "odontoma", "shortest_name_length": 8}
{"curie": "MONDO:0019643", "names": ["TPHA", "Transient pseudohypoaldosteronism", "transient pseudohypoaldosteronism", "Secondary pseudohypoaldosteronism", "Transient pseudohypoaldosteronism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transient pseudohypoaldosteronism", "shortest_name_length": 4}
{"curie": "MONDO:0022606", "names": ["branchial arch disease", "pharyngeal system development disease", "disease of pharyngeal system development", "disorder of pharyngeal system development"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "branchial arch disease", "shortest_name_length": 22}
{"curie": "MONDO:0100249", "names": ["SRXX", "XX sex reversal", "XX Sex Reversal", "Sex Reversal, XX", "XX Male Syndrome", "Reversal, XX Sex", "XX male syndrome", "XX Sex Reversals", "Syndrome, XX Male", "Reversals, XX Sex", "XX Male Syndromes", "Sex Reversals, XX", "XX, male syndrome", "Syndromes, XX Male", "46,XX sex reversal", "46,XX testicular DSD", "46,XX Testicular DSD", "46, XX Testicular DSD", "XX Male, Sry-positive", "De la Chapelle syndrome", "46,XX gonadal dysgenesis", "46, XX gonadal sex reversal", "46,XX testicular disorder of sex development", "46,XX testicular disorders of Sex development", "46,XX Testicular Disorders of Sex Development", "46, XX Testicular Disorder of Sex Development", "46, XX Testicular Disorders of Sex Development", "46,XX Testicular Differences of Sex Development", "46,XX testicular differences of sex development", "46,XX testicular disorder of sex development (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XX testicular disorder of sex development", "shortest_name_length": 4}
{"curie": "UMLS:C2825129", "names": ["APL with t(11;17)(q23;q21); PLZF-RARA", "APL with t(11;17)(q23;q21); ZBTB16-RARA", "Acute Myeloid Leukemia with t(11;17)(q23;q21)", "Acute Promyelocytic Leukemia with t(11;17)(q23;q21); PLZF-RARA", "Acute Promyelocytic Leukemia with t(11;17)(q23;q21); ZBTB16-RARA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Myeloid Leukemia with t(11;17)(q23;q21)", "shortest_name_length": 37}
{"curie": "MONDO:0008245", "names": ["Telfer Sugar Jaeger syndrome", "telfer Sugar Jaeger syndrome", "Telfer-Sugar-Jaeger syndrome", "telfer-Sugar-Jaeger syndrome", "piebald trait neurologic defects", "Piebald trait neurologic defects", "PIEBALD TRAIT WITH NEUROLOGIC DEFECTS", "piebald trait with neurologic defects", "piebald trait-neurologic defects syndrome", "Piebald trait-neurologic defects syndrome", "Piebald trait with neurologic defects syndrome", "Piebald trait with neurologic defects syndrome (disorder)", "White forelock and leukoderma with neurological impairment", "Piebald trait with neurologic defects syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "piebald trait-neurologic defects syndrome", "shortest_name_length": 28}
{"curie": "UMLS:C2938864", "names": ["Drug administered in wrong device"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drug administered in wrong device", "shortest_name_length": 33}
{"curie": "MONDO:0019360", "names": ["RICKETTSIALPOX", "rickettsialpox", "Rickettsialpox", "pox rickettsial", "rickettsial pox", "Kew Garden fever", "Kew Garden; fever", "fever; Kew Garden", "Rickettsia; smallpox", "Vesicular rickettsiosis", "vesicular rickettsiosis", "rickettsiosis; vesicular", "vesicular; rickettsiosis", "Kew Gardens spotted fever", "Kew Garden; spotted fever", "Rickettsialpox (disorder)", "spotted fever; Kew Garden", "rickettsialpox (diagnosis)", "Rickettsia akari infection", "Rickettsia akari Infection", "Rickettsia; akari, smallpox", "Rickettsia akari Infections", "Infection, Rickettsia akari", "Infections, Rickettsia akari", "Rickettsia akari spotted fever", "smallpox; due to Rickettsia akari", "Rickettsialpox due to Rickettsia akari"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rickettsialpox", "shortest_name_length": 14}
{"curie": "MONDO:0008972", "names": ["Pbd9", "PBD9", "Rcdp1", "RCDP1", "peroxisome biogenesis disorder 9", "PEROXISOME BIOGENESIS DISORDER 9", "Peroxisome Biogenesis Disorder 9", "CHONDRODYSTROPHIA CALCIFICANS PUNCTATA", "chondrodystrophia calcificans punctata", "Chondrodystrophia calcificans punctata", "PEX7 rhizomelic chondrodysplasia punctata", "chondrodysplasia punctata, rhizomelic form", "Rhizomelic chondrodysplasia punctata type 1", "rhizomelic chondrodysplasia punctata type 1", "rhizomelic chondrodysplasia punctata, type 1", "RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1", "Rhizomelic chondrodysplasia punctata, type 1", "Rhizomelic chondrodysplasia punctata type 1 (disorder)", "rhizomelic chondrodysplasia punctata type 1 (diagnosis)", "rhizomelic chondrodysplasia punctata caused by mutation in PEX7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rhizomelic chondrodysplasia punctata type 1", "shortest_name_length": 4}
{"curie": "UMLS:C4505291", "names": ["Xp21 Contiguous Gene Deletion Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Xp21 Contiguous Gene Deletion Syndrome", "shortest_name_length": 38}
{"curie": "MONDO:0014531", "names": ["ALS22", "ALS 22", "amyotrophic lateral sclerosis 22", "TUBA4A amyotrophic lateral sclerosis", "amyotrophic lateral sclerosis type 22", "amyotrophic lateral sclerosis caused by mutation in TUBA4A", "AMYOTROPHIC LATERAL SCLEROSIS 22 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA", "amyotrohpic lateral sclerosis 22 with or without frontotemporal dementia", "amyotrophic lateral sclerosis 22 with or without frontotemporal dementia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyotrophic lateral sclerosis type 22", "shortest_name_length": 5}
{"curie": "MONDO:0009611", "names": ["MGA4", "MGCA4", "MGA Type IV", "MGA type IV", "Mga, type 4", "MGA, TYPE IV", "3-methylglutaconic aciduria type 4", "3-Methylglutaconic aciduria type 4", "3-Methylglutaconic aciduria, type 4", "3-Methylglutaconic Aciduria Type IV", "3-methylglutaconic aciduria type IV", "3 methylglutaconic aciduria type IV", "3-METHYLGLUTACONIC ACIDURIA, TYPE IV", "3-METHYLGLUTACONIC aciduria, type IV", "Not otherwise specified 3-MGA-Uria type", "3 alpha methylglutaconic aciduria type IV", "3-Methylglutaconic aciduria type 4 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "3-methylglutaconic aciduria type 4", "shortest_name_length": 4}
{"curie": "MONDO:0003134", "names": ["Glomerulonephritis proliferative", "proliferative glomerulonephritis", "Proliferative glomerulonephritis", "GLOMERULONEPHRITIS PROLIFERATIVE", "Proliferative Glomerulonephritis", "Glomerulonephritis, proliferative", "Proliferative glomerulonephritis NOS", "Proliferative glomerulonephritis (disorder)", "proliferative glomerulonephritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "proliferative glomerulonephritis", "shortest_name_length": 32}
{"curie": "MONDO:0013053", "names": ["Hadziselimovic syndrome", "HADZISELIMOVIC SYNDROME", "Hadziselimovic Syndrome", "Microcephaly-Faciocardioskeletal Syndrome", "microcephaly-faciocardioskeletal syndrome", "MICROCEPHALY-FACIOCARDIOSKELETAL SYNDROME", "Microcephaly-faciocardioskeletal syndrome", "Microcephaly faciocardioskeletal syndrome", "Microcephaly-facio-cardio-skeletal syndrome, Hadziselimovic type", "Microcephalus facio-cardio-skeletal syndrome Hadziselimovic type", "microcephaly-facio-cardio-skeletal syndrome, Hadziselimovic type", "Microcephalus facio-cardio-skeletal syndrome Hadziselimovic type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly-facio-cardio-skeletal syndrome, Hadziselimovic type", "shortest_name_length": 23}
{"curie": "MONDO:0013258", "names": ["AUTS16", "autism susceptibility 16", "susceptibility to autism 16", "AUTISM, SUSCEPTIBILITY TO, 16", "autism, susceptibility to, 16", "autism with or without seizures", "AUTISM WITH OR WITHOUT SEIZURES", "autism, susceptibility to, type 16"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autism, susceptibility to, 16", "shortest_name_length": 6}
{"curie": "MONDO:0016552", "names": ["congenital primary megaureter, nonrefluxing and unobstructed form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital primary megaureter, nonrefluxing and unobstructed form", "shortest_name_length": 65}
{"curie": "MONDO:0005728", "names": ["diaphragm disease", "diaphragm diseases", "diaphragm disorder", "disorder diaphragm", "diaphragm; disorder", "diaphragm disorders", "Disease of diaphragm", "disease of diaphragm", "Diaphragmatic disease", "disorder of diaphragm", "diaphragmatic disease", "Disorder of diaphragm", "Disorders of diaphragm", "diaphragmatic disorder", "Diaphragmatic disorder", "Diaphragmatic disorders", "DISEASES OF THE DIAPHRAGM", "diseases of the diaphragm", "Disease of diaphragm, NOS", "Diaphragmatic disorder NOS", "diaphragm disease or disorder", "disease or disorder of diaphragm", "Disorder of diaphragm (disorder)", "disease (or disorder); diaphragm", "Diaphragmatic disorders (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diaphragm disorder", "shortest_name_length": 17}
{"curie": "MONDO:0006730", "names": ["Drug Psychoses", "Psychosis;drug", "Drug psychosis", "psychosis drug", "drug psychosis", "Toxic Psychoses", "drugs psychosis", "Psychosis, drug", "Psychoses, Drug", "Toxic psychoses", "Psychoses, Toxic", "drug induced psychosis", "Drug-induced psychosis", "drug-induced psychosis", "psychosis drug-induced", "Drug induced psychosis", "Substance Induced Psychoses", "Substance-Induced Psychoses", "Psychoses, Substance Induced", "Psychoses, Substance-Induced", "Drug-induced psychotic disorder", "drug-induced psychotic disorder", "Drug-induced psychotic disorders", "Psychotic disorder caused by drug", "Drug-induced psychosis (diagnosis)", "Psychotic disorder caused by drug (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "drug psychosis", "shortest_name_length": 14}
{"curie": "UMLS:C0341339", "names": ["radiation colitis", "Radiation colitis", "Radiation Colitis", "colitis; radiation", "radiation; colitis", "Colitis due to radiation", "colitis due to radiation", "Radiation induced colitis", "Colitis caused by radiation", "radiation colitis (diagnosis)", "Colitis caused by radiation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colitis due to radiation", "shortest_name_length": 17}
{"curie": "MONDO:0005554", "names": ["RHEUMATIC", "Rheumatism", "Rheumatics", "RHEUMATISM", "rheumatism", "rheumatics", "enthesopathy", "enthesopathies", "Rheumatism, NOS", "Collagen Disease", "Collagen disease", "collagen disease", "Disease;collagen", "COLLAGEN DISEASE", "COLLAGEN DISORDER", "collagen disorder", "rheumatic disease", "collagen diseases", "Disease, Collagen", "Collagen diseases", "Collagen disorder", "Collagen Diseases", "Rheumatic Disease", "COLLAGEN DISORDERS", "Disease, Rheumatic", "Diseases, Collagen", "rheumatic diseases", "Rheumatic Diseases", "rheumatic disorder", "disease, rheumatic", "collagen disorders", "diseases, rheumatic", "Diseases, Rheumatic", "Collagen disease NOS", "Collagen disease, NOS", "Collagen disorder NOS", "Rheumatologic Disease", "RHEUMATOLOGIC PROBLEM", "Rheumatism (disorder)", "rheumatologic disorder", "Rheumatologic Disorder", "rheumatism (diagnosis)", "Collagen disorder, NOS", "Disorder collagen (NOS)", "COLLAGEN DISORDER (NOS)", "Inflammatory Rheumatism", "Rheumatism, unspecified", "inflammatory rheumatism", "Locomotor pain disorder", "DISORDER COLLAGEN (NOS)", "Collagen Vascular Disease", "collagen vascular disease", "connective tissue disease", "Connective Tissue Disease", "Collagen disease (disorder)", "Musculoskeletal pain disorder", "Musculoskeletal Pain Disorder", "musculoskeletal pain disorder", "rheumatologic disorder (diagnosis)", "Diffuse disease of connective tissue", "Diffuse diseases of connective tissue", "Rheumatism, unspecified, site unspecified", "Diffuse disease of connective tissue, NOS", "Unspecified diffuse connective tissue disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rheumatic disorder", "shortest_name_length": 9}
{"curie": "MONDO:0002629", "names": ["OSRC", "bone cancer", "osteosarcoma", "bone sarcoma", "Osteosarcoma", "OSTEOSARCOMA", "Osteosarcomas", "bone sarcomas", "osteosarcomas", "osteoid sarcoma", "Bone cell cancer", "Osteosarcoma NOS", "bone osteosarcoma", "Osteosarcoma, NOS", "Bone Osteosarcoma", "SARCOMA OSTEOGENIC", "osteogenic sarcoma", "OSTEOGENIC SARCOMA", "Sarcoma osteogenic", "Osteogenic sarcoma", "Osteosarcoma Tumor", "Osteogenic Sarcoma", "sarcoma, osteogenic", "[M]Osteosarcoma NOS", "Osteogenic Sarcomas", "Osteosarcoma Tumors", "Tumor, Osteosarcoma", "Sarcoma, Osteogenic", "osteochondrosarcoma", "Osteochondrosarcoma", "Osteoblastic sarcoma", "Tumors, Osteosarcoma", "Osteosarcoma of Bone", "Osteosarcoma of bone", "Sarcomas, Osteogenic", "osteosarcoma of bone", "osteosarcoma, somatic", "Osteogenic sarcoma, NOS", "OSTEOSARCOMA, MALIGNANT", "Osteoblastic osteosarcoma", "primary osteosarcoma of bone", "primary Osteosarcoma of bone", "osteosarcoma, somatic mutation", "BONE CANCER, OSTEOGENIC SARCOMA", "Osteosarcoma of bone (disorder)", "osteosarcoma of bone (diagnosis)", "Osteosarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bone osteosarcoma", "shortest_name_length": 4}
{"curie": "MONDO:0014801", "names": ["EVPLS", "EVEN-plus syndrome", "even-plus syndrome", "EVEN-PLUS SYNDROME", "Epiphysial-vertebral-ear dysplasia-nose-plus associated findings syndrome", "epiphysial-vertebral-ear dysplasia-nose-plus associated findings syndrome", "epiphyseal and vertebral dysplasia, microtia, and flat Nose, plus associated malformations", "EPIPHYSEAL AND VERTEBRAL DYSPLASIA, MICROTIA, AND FLAT NOSE, PLUS ASSOCIATED MALFORMATIONS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "even-plus syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0029133", "names": ["LGMD1I", "LGMDD4", "LGMD type D4", "Limb-girdle muscular dystrophy type D4", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1I", "muscular dystrophy, limb-girdle, type 1I", "Calpain-3-related limb-girdle muscular dystrophy D4", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 4", "muscular dystrophy, limb-girdle, autosomal dominant 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy, limb-girdle, autosomal dominant 4", "shortest_name_length": 6}
{"curie": "MONDO:0001694", "names": ["Diffuse interstitial keratitis", "diffuse interstitial keratitis", "Diffuse interstitial keratitis (disorder)", "diffuse interstitial keratitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diffuse interstitial keratitis", "shortest_name_length": 30}
{"curie": "UMLS:C4684949", "names": ["NF Type 1 with Inoperable, Progressive, Symptomatic Plexiform Neurofibromas", "Neurofibromatosis Type 1 with Inoperable, Progressive, Symptomatic Plexiform Neurofibromas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neurofibromatosis Type 1 with Inoperable, Progressive, Symptomatic Plexiform Neurofibromas", "shortest_name_length": 75}
{"curie": "MONDO:0012933", "names": ["HBOC2", "BROVCA2", "breast-ovarian cancer, familial, 2", "BREAST CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2", "breast cancer, familial, susceptibility to, 2", "OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2", "ovarian cancer, familial, susceptibility to, 2", "BRCA2 hereditary breast ovarian cancer syndrome", "susceptibility to familial breast-ovarian cancer 2", "breast-ovarian cancer, familial, susceptibility to, 2", "BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2", "breast-ovarian cancer, familial, susceptibility to, type 2", "hereditary breast ovarian cancer syndrome caused by mutation in BRCA2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast-ovarian cancer, familial, susceptibility to, 2", "shortest_name_length": 5}
{"curie": "MONDO:0012813", "names": ["RP29", "RP 29", "RETINITIS PIGMENTOSA 29", "Retinitis Pigmentosa 29", "retinitis pigmentosa 29", "retinitis pigmentosa type 29", "RETINITIS PIGMENTOSA 29 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 29", "shortest_name_length": 4}
{"curie": "MONDO:0024245", "names": ["Carcinoma Simplex", "carcinoma simplex", "Carcinoma simplex", "hidradenocarcinoma", "anaplastic syringoma", "Anaplastic syringoma", "malignant hidradenoma", "malignant acrospiroma", "Malignant acrospiroma", "Ductal Eccrine Carcinoma", "ductal eccrine carcinoma", "eccrine ductal carcinoma", "Eccrine ductal carcinoma", "ductal eccrine adenocarcinoma", "carcinoma simplex (diagnosis)", "Ductal Eccrine Adenocarcinoma", "Malignant eccrine acrospiroma", "Eccrine ductal carcinoma of skin", "eccrine ductal carcinoma of skin", "sweat gland carcinoma of the hand", "primary mucoepidermoid cutaneous carcinoma", "Carcinoma simplex (morphologic abnormality)", "Eccrine ductal carcinoma of skin (disorder)", "Eccrine ductal carcinoma of skin (diagnosis)", "Eccrine ductal carcinoma (morphologic abnormality)", "eccrine ductal carcinoma (morphologic abnormality)", "skin neoplasm malignant adnexa with eccrine differentiation ductal carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ductal eccrine adenocarcinoma", "shortest_name_length": 17}
{"curie": "UMLS:C3272534", "names": ["Small Intestinal NET G2", "Small Intestinal Neuroendocrine Tumor G2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Intestinal Neuroendocrine Tumor G2", "shortest_name_length": 23}
{"curie": "UMLS:C4744761", "names": ["Thyroid Gland Solitary Fibrous Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Solitary Fibrous Tumor", "shortest_name_length": 36}
{"curie": "MONDO:0007152", "names": ["ARVC1", "ARVD1", "Uhl anomaly", "cardiomyopathy, right ventricular dilated", "Cardiomyopathy, Right Ventricular Dilated", "CARDIOMYOPATHY, RIGHT VENTRICULAR DILATED", "arrhythmogenic right ventricular dysplasia 1", "arrhythmogenic right ventricular cardiomyopathy 1", "arrhythmogenic right ventricular dysplasia type 1", "ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 1", "Arrhythmogenic Right Ventricular Cardiomyopathy 1", "TGFB3 arrhythmogenic right ventricular cardiomyopathy", "familial arrhythmogenic right ventricular dysplasia 1", "ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 1", "arrhythmogenic right ventricular dysplasia, familial, 1", "Arrhythmogenic Right Ventricular Dysplasia, Familial, 1", "arrhythmogenic right ventricular dysplasia, familial, type 1", "ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 1 (disorder)", "arrhythmogenic right ventricular cardiomyopathy caused by mutation in TGFB3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arrhythmogenic right ventricular dysplasia 1", "shortest_name_length": 5}
{"curie": "UMLS:C1328375", "names": ["Application site discomfort"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Application site discomfort", "shortest_name_length": 27}
{"curie": "UMLS:C1521844", "names": ["DHL", "diffuse histiocytic lymphoma (DHL)", "DHL (diffuse histiocytic lymphoma)", "Malignant Lymphoma, Histiocytic, Diffuse", "Malignant lymphoma, histiocytic, diffuse", "diffuse histiocytic malignant lymphoma (DHL)", "diffuse histiocytic malignant lymphoma (DHL) (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Lymphoma, Histiocytic, Diffuse", "shortest_name_length": 3}
{"curie": "UMLS:C0796620", "names": ["stage IIB soft tissue sarcoma", "Stage IIB Soft Tissue Sarcoma", "Stage IIB Sarcoma of Soft Tissue", "Stage IIB Sarcoma of the Soft Tissue", "Stage IIB Soft Tissue Sarcoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Soft Tissue Sarcoma AJCC v7", "shortest_name_length": 29}
{"curie": "MONDO:0042970", "names": ["glutamate decarboxylase deficiency", "disorder of glutamate decarboxylase", "deficiency of glutamate decarboxylase", "Deficiency of glutamate decarboxylase", "glutamate decarboxylase activity disease", "disorder of glutamate decarboxylase activity", "Deficiency of glutamate decarboxylase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of glutamate decarboxylase", "shortest_name_length": 34}
{"curie": "UMLS:C1096049", "names": ["Infusion site swelling", "Infusion site swelling (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infusion site swelling", "shortest_name_length": 22}
{"curie": "UMLS:C2348737", "names": ["Mixed", "Gastric Mixed Adenocarcinoma", "mixed adenocarcinoma of the stomach", "stomach, mixed adenocarcinoma of the", "gastric cancer, mixed adenocarcinoma", "stomach cancer, mixed adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Mixed Adenocarcinoma", "shortest_name_length": 5}
{"curie": "UMLS:C3805116", "names": ["Benign ethnic neutropenia", "Constitutional neutropenia", "Benign ethnic neutropenia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign ethnic neutropenia", "shortest_name_length": 25}
{"curie": "UMLS:C0340016", "names": ["Traumatic chylothorax", "Traumatic Chylothorax", "Traumatic chylothorax (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Traumatic chylothorax", "shortest_name_length": 21}
{"curie": "MONDO:0004751", "names": ["Orbital disease", "disease orbital", "orbital disease", "Orbital Disease", "Disease, Orbital", "orbital disorder", "Orbital Diseases", "Diseases, Orbital", "Disorder of orbit", "disorder of orbit", "Disorders of orbit", "disorders of orbit", "Orbital disorder NOS", "Disorders of the orbit", "DISORDERS OF THE ORBIT", "Disorder of orbit, NOS", "Disorder of orbit proper", "disease (or disorder); orbit", "Unspecified disorder of orbit", "Disorder of orbit, unspecified", "disorders of orbit (diagnosis)", "Disorder of orbit proper (disorder)", "disease of orbital part of eye adnexa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disease of orbital part of eye adnexa", "shortest_name_length": 15}
{"curie": "MONDO:0031002", "names": ["BARMACS", "BARALLE-MACKEN SYNDROME", "Baralle-Macken syndrome", "neurodevelopmental disorder with cataracts and variable microcephaly", "NEURODEVELOPMENTAL DISORDER WITH CATARACTS AND VARIABLE MICROCEPHALY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Baralle-Macken syndrome", "shortest_name_length": 7}
{"curie": "MONDO:0002526", "names": ["unilateral segmental cavernous hemangioma", "Unilateral segmental cavernous hemangioma", "Unilateral segmental cavernous haemangioma", "dermal unilateral segmental cavernous angioma", "Unilateral Segmental Cavernous hemangioma of the skin", "unilateral segmental cavernous hemangioma of the skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermal unilateral segmental cavernous angioma", "shortest_name_length": 41}
{"curie": "MONDO:0003366", "names": ["HYDRARTHROSIS", "Hydrarthrosis", "hydrarthrosis", "Hydrarthroses", "joint effusion", "Joint effusion", "effusion joint", "Joint Effusion", "JOINT EFFUSION", "effusion joints", "effusions joint", "synovial effusion", "SYNOVIAL EFFUSION", "Joint(s) Effusion", "effusion synovial", "effusion of joint", "Effusion;joint(s)", "Effusion of joint", "Hydrarthrosis, NOS", "Effusion into joint", "Joint fluid increased", "Effusion of joint, NOS", "hydrarthrosis (diagnosis)", "Effusion of joint (disorder)", "Effusion of joint, site unspecified", "Effusion of joint, other specified sites"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hydrarthrosis", "shortest_name_length": 13}
{"curie": "MONDO:0008029", "names": ["BTHLM1", "LGMDD5", "Bethlem myopathy", "BETHLEM MYOPATHY", "BETHLEM MYOPATHY 1", "Bethlem Myopathy 1", "Bethlem myopathy 1", "Bethlem myopathy type 1", "Bethlem myopathy (disorder)", "Benign autosomal dominant myopathy", "benign autosomal dominant myopathy", "Benign Congenital Muscular Dystrophy", "benign congenital muscular dystrophy", "MUSCULAR DYSTROPHY, BENIGN CONGENITAL", "Muscular dystrophy, benign congenital", "Benign Congenital Myopathy with Contractures", "Myopathy, benign congenital, with contractures", "MYOPATHY, BENIGN CONGENITAL, WITH CONTRACTURES", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bethlem myopathy", "shortest_name_length": 6}
{"curie": "UMLS:C0729233", "names": ["Thoracic", "aorta dissection thoracic", "Thoracic Aorta Dissection", "Dissection, Thoracic Aorta", "Thoracic aortic dissection", "Aorta Dissection, Thoracic", "Thoracic Aorta Dissections", "Thoracic Aortic Dissection", "Thoracic Aortic Dissections", "Aortic Dissection, Thoracic", "Dissection, Thoracic Aortic", "Dissection of thoracic aorta", "dissection of thoracic aorta", "Dissection of aorta, thoracic", "AORTA THORACIC ANEURYSM DISSECTING", "Dissecting Thoracic Aortic Aneurysm", "Dissecting aortic aneurysm, thoracic", "aorta thoracic; aneurysm, dissecting", "aneurysm; thoracic aorta, dissecting", "Dissection of thoracic aorta (disorder)", "dissection of thoracic aorta (diagnosis)", "Dissection of thoracic aorta, unspecified", "Dissecting aneurysm of the thoracic aorta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dissecting aneurysm of the thoracic aorta", "shortest_name_length": 8}
{"curie": "MONDO:0016120", "names": ["Myotonic disorder", "Myotonic Disorder", "myotonic myopathy", "myotonic disorder", "myotonic syndrome", "Myotonic Myopathy", "Myotonic Disorders", "Disorder, Myotonic", "myotonic disorders", "Myopathy, Myotonic", "myotonic; disorder", "Myotonic disorders", "Disorders, Myotonic", "Myotonic Myopathies", "Myopathies, Myotonic", "Myotonic disorder (disorder)", "Myotonic disease or syndrome", "Myotonic Diseases and Syndromes", "disease (or disorder); myotonic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myotonic syndrome", "shortest_name_length": 17}
{"curie": "MONDO:0013837", "names": ["COQ10D2", "primary coenzyme Q10 deficiency 2", "coenzyme Q10 deficiency, primary, 2", "COENZYME Q10 DEFICIENCY, PRIMARY, 2", "coenzyme Q10 deficiency, primary, type 2", "deafness-encephaloneuropathy-obesity-valvulopathy syndrome", "hearing loss-encephaloneuropathy-obesity-valvulopathy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness-encephaloneuropathy-obesity-valvulopathy syndrome", "shortest_name_length": 7}
{"curie": "MONDO:0018827", "names": ["familial chilblain lupus", "hereditary chilblain lupus", "hereditary Chilblain lupus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial chilblain lupus", "shortest_name_length": 24}
{"curie": "MONDO:0008676", "names": ["WSN1", "WHITE SPONGE NEVUS 1", "white sponge nevus 1", "WHITE sponge NEVUS 1", "White sponge Nevus type 1", "White sponge Nevus of Cannon", "leukokeratosis, hereditary mucosal", "KRT4 hereditary mucosal leukokeratosis", "hereditary mucosal leukokeratosis caused by mutation in KRT4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "white sponge nevus 1", "shortest_name_length": 4}
{"curie": "UMLS:C4520903", "names": ["Stage 0 Lung Adenocarcinoma", "Lung Adenocarcinoma in situ", "Adenocarcinoma in situ of Lung", "Adenocarcinoma in situ of the Lung", "Stage 0 Lung Adenocarcinoma AJCC v6", "Stage 0 Lung Adenocarcinoma AJCC v7", "Stage 0 Lung Adenocarcinoma AJCC v6 and v7", "Lung Adenocarcinoma, Stage 0 AJCC v6 and v7", "Stage 0 Adenocarcinoma of Lung AJCC v6 and v7", "Stage 0 Adenocarcinoma of the Lung AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Lung Adenocarcinoma AJCC v6 and v7", "shortest_name_length": 27}
{"curie": "MONDO:0019751", "names": ["Autoinflammatory disease", "autoinflammatory disease", "Autoinflammatory Syndrome", "autoinflammatory syndrome", "Autoinflammatory syndrome", "Autoinflammatory diseases", "Autoinflammatory syndromes", "Autoinflammatory disease (disorder)", "autoinflammatory disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoinflammatory syndrome", "shortest_name_length": 24}
{"curie": "UMLS:C4721791", "names": ["Stage IC Ovarian Cancer", "Ovarian Cancer Stage IC", "AJCC Stage IC Ovarian Cancer", "FIGO Stage IC Ovarian Cancer", "FIGO Stage IC Cancer of Ovary", "FIGO Stage IC Ovarian Carcinoma", "Stage IC Ovarian Cancer AJCC v7", "Stage IC Ovarian Cancer AJCC v6", "FIGO Stage IC Carcinoma of Ovary", "FIGO Stage IC Cancer of the Ovary", "Stage IC Ovarian Epithelial Cancer", "FIGO Stage IC Carcinoma of the Ovary", "Stage IC Ovarian Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IC Ovarian Cancer AJCC v6 and v7", "shortest_name_length": 23}
{"curie": "UMLS:C1335001", "names": ["Non-Neoplastic Chest Wall Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Chest Wall Disorder", "shortest_name_length": 34}
{"curie": "MONDO:0001735", "names": ["Sinus disease", "sinus disorder", "Sinus disorder", "disorders sinus", "Sinus disorder NOS", "Disorder of nasal sinus", "paranasal sinus disease", "Paranasal Sinus Disease", "disorder of nasal sinus", "paranasal sinus disorder", "Disease, Paranasal Sinus", "diseases paranasal sinus", "Sinus Disease, Paranasal", "paranasal sinus diseases", "Paranasal Sinus Diseases", "Paranasal Sinus Disorder", "Sinus Diseases, Paranasal", "disorder of nasal sinuses", "Diseases, Paranasal Sinus", "Disease of accessory sinus", "disease of paranasal sinus", "Paranasal sinuses--Diseases", "disorder of paranasal sinus", "Disease of nasal sinus, NOS", "DISEASES OF THE NASAL SINUSES", "Disorder of paranasal sinuses", "Disease of accessory sinus, NOS", "Disorder of nasal sinus (disorder)", "paranasal sinus disease or disorder", "disorder of nasal sinuses (diagnosis)", "disease or disorder of paranasal sinus", "Disease or syndrome of the paranasal sinuses", "DISEASES OF THE NASAL SINUSES: GENERAL TERMS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paranasal sinus disorder", "shortest_name_length": 13}
{"curie": "MONDO:0008350", "names": ["PULMONIC STENOSIS AND DEAFNESS", "pulmonic stenosis and deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonic stenosis and deafness", "shortest_name_length": 30}
{"curie": "MONDO:0006061", "names": ["cervical artery dissection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical artery dissection", "shortest_name_length": 26}
{"curie": "UMLS:C0238141", "names": ["Gum Carcinoma", "Carcinoma of Gum", "gingival carcinoma", "Gingival Carcinoma", "GINGIVA, CARCINOMA", "carcinoma of gingiva", "Carcinoma of Gingiva", "Carcinoma of the Gum", "Carcinoma of the Gingiva", "GINGIVAL CANCER, CARCINOMA", "carcinoma of gingiva (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma of gingiva", "shortest_name_length": 13}
{"curie": "MONDO:0017139", "names": ["Oroacral syndrome", "oromandibular-limb hypogenesis syndrome", "oro-mandibular-limb hypogenesis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oromandibular-limb hypogenesis syndrome", "shortest_name_length": 17}
{"curie": "MONDO:0005906", "names": ["QUINSY", "quinsy", "Quinsy", "quinsies", "angina tonsillary", "QUINSY SORE THROAT", "tonsillaris angina", "Angina tonsillaris", "Peritonsillar Abscess", "Abscess;peritonsillar", "Peritonsillar abscess", "Abscess peritonsillar", "PERITONSILLAR ABSCESS", "peritonsillar abscess", "abscess; peritonsillar", "peritonsillar; abscess", "Abscess, Peritonsillar", "ABSCESS, PERITONSILLAR", "Peritonsillar Abscesses", "Abscesses, Peritonsillar", "Peritonsillar abscess NOS", "quinsy peritonsillar abscess", "tonsils peritonsillar abscess", "Peritonsillar abscess (disorder)", "peritonsillar abscess (diagnosis)", "quinsy peritonsillar abscess (diagnosis)", "peritonsillar abscess (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peritonsillar abscess", "shortest_name_length": 6}
{"curie": "MONDO:0054748", "names": ["FANCS", "Fanconi anemia, complementation GROUP S", "FANCONI ANEMIA, COMPLEMENTATION GROUP S", "Fanconi anemia, complementation group S"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fanconi anemia, complementation group S", "shortest_name_length": 5}
{"curie": "MONDO:0013323", "names": ["CED2", "CRANIOECTODERMAL dysplasia 2", "CRANIOECTODERMAL DYSPLASIA 2", "cranioectodermal dysplasia 2", "WDR35 cranioectodermal dysplasia", "Cranioectodermal dysplasia type 2", "cranioectodermal dysplasia caused by mutation in WDR35"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cranioectodermal dysplasia 2", "shortest_name_length": 4}
{"curie": "MONDO:0012778", "names": ["CELIAC9", "CELIAC DISEASE, SUSCEPTIBILITY TO, 9", "celiac disease, susceptibility to, 9", "gluten-sensitive enteropathy, susceptibility to, 9", "GLUTEN-SENSITIVE ENTEROPATHY, SUSCEPTIBILITY TO, 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "celiac disease, susceptibility to, 9", "shortest_name_length": 7}
{"curie": "MONDO:0044781", "names": ["SSNS", "Steroid Sensitive Nephrotic Syndrome", "nephrotic syndrome steroid-sensitive", "Steroid-sensitive nephrotic syndrome", "Steroid-Sensitive Nephrotic Syndrome", "steroid-sensitive nephrotic syndrome", "Steroid-responsive nephrotic syndrome", "Steroid-Sensitive Nephrotic Syndromes", "Syndrome, Steroid-Sensitive Nephrotic", "steroid-responsive nephrotic syndrome", "Nephrotic Syndrome, Steroid-Sensitive", "Steroid-Responsive Nephrotic Syndrome", "SSNS - Steroid-sensitive nephrotic syndrome", "Idiopathic steroid-sensitive nephrotic syndrome", "Steroid-sensitive nephrotic syndrome (disorder)", "Steroid-sensitive nephrotic syndrome (diagnosis)", "Steroid sensitive nephrotic syndrome of childhood", "Nephrotic Syndrome of Childhood - Steroid Sensitive", "nephrotic syndrome of childhood - steroid sensitive", "Steroid sensitive nephrotic syndrome of childhood (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrotic syndrome of childhood - steroid sensitive", "shortest_name_length": 4}
{"curie": "MONDO:0016304", "names": ["PKAN, classic form", "NBIA1, classic form", "classic pantothenate kinase-associated neurodegeneration", "neurodegeneration with brain iron accumulation type 1, classic form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "classic pantothenate kinase-associated neurodegeneration", "shortest_name_length": 18}
{"curie": "UMLS:C0003534", "names": ["Aphakia", "aphakia", "APHAKIA", "Aphakias", "Aphakic Eye", "lens; absent", "Eye, Aphakic", "Aphakic Eyes", "absence; lens", "Absence of lens", "Aphakia (disorder)", "aphakia (diagnosis)", "aphakia was observed", "aphakia (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aphakia", "shortest_name_length": 7}
{"curie": "MONDO:0021180", "names": ["acquired xanthinuria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired xanthinuria", "shortest_name_length": 20}
{"curie": "UMLS:C0085628", "names": ["stupor", "STUPOR", "obtund", "Stupor", "obtunded", "Stuporous", "Obtundation", "OBTUNDATION", "obtundation", "Stupor (finding)", "Obtundation mental", "stupor was observed", "Mental status, stupor", "stupor (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stupor", "shortest_name_length": 6}
{"curie": "MONDO:0021285", "names": ["Stage 0is Urethral Cancer", "urethra in situ carcinoma", "urethra carcinoma in situ", "stage 0is urethral cancer", "stage 0 urethra carcinoma", "Urethra Carcinoma in situ", "urethral carcinoma in situ", "Urethral Carcinoma in situ", "stage 0is urethra carcinoma", "Stage 0is Urethra Carcinoma", "carcinoma in situ of urethra", "stage 0is urethral carcinoma", "Stage 0is Urethral Carcinoma", "Carcinoma in situ of Urethra", "Carcinoma in situ of urethra", "Stage 0is Carcinoma of Urethra", "stage 0is carcinoma of urethra", "Carcinoma in situ of the Urethra", "carcinoma in situ of the urethra", "stage 0is urethral cancer aJCC v7", "Stage 0is Urethral Cancer AJCC v7", "Stage 0is Carcinoma of the Urethra", "CIS - Carcinoma in situ of urethra", "stage 0is carcinoma of the urethra", "Carcinoma in situ of urethra (disorder)", "carcinoma in situ of urethra (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma in situ of urethra", "shortest_name_length": 25}
{"curie": "UMLS:C3830466", "names": ["Disseminated Oka VZV Infection", "Disseminated Oka Varicella Zoster Virus Infection", "Disseminated varicella zoster vaccine virus infection", "Disseminated Varicella Zoster Vaccine Virus Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disseminated varicella zoster vaccine virus infection", "shortest_name_length": 30}
{"curie": "UMLS:C1335050", "names": ["Non-Neoplastic Urethra Disease", "Non-Neoplastic Urethra Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Urethra Disorder", "shortest_name_length": 30}
{"curie": "MONDO:0006328", "names": ["Odontogenic cyst", "Odontogenic Cyst", "odontogenic cyst", "Cyst, Odontogenic", "odontogenic cysts", "odontogenic; cyst", "Odontogenic Cysts", "Cyst, odontogenic", "cyst; odontogenic", "Odontogenic cysts", "Cysts, Odontogenic", "Odontogenic cyst, NOS", "Odontogenic cyst (disorder)", "Developmental odontogenic cyst", "Developmental odontogenic cyst, NOS", "Odontogenic cyst (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "odontogenic cyst", "shortest_name_length": 16}
{"curie": "MONDO:0018360", "names": ["neonatal SLE", "neonatal lupus", "Neonatal lupus", "congenital lupus", "Neonatal lupus syndrome", "neonatal lupus syndrome", "Neonatal lupus erythematosus", "Neonatal Lupus Erythematosus", "neonatal lupus erythematosus", "lupus erythematosus neonatal", "congenital lupus erythematosus", "Neonatal Systemic lupus erythematosus", "neonatal systemic lupus erythematosus", "Neonatal lupus erythematosus (disorder)", "neonatal lupus erythematosus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal lupus erythematosus", "shortest_name_length": 12}
{"curie": "MONDO:0010608", "names": ["Hhhh Syndrome", "HHHH SYNDROME", "Hhhh syndrome", "hereditary Hemihypotrophy hemiparesis hemiathetosis syndrome", "Hereditary Hemihypotrophy Hemiparesis Hemiathetosis Syndrome", "HEREDITARY HEMIHYPOTROPHY HEMIPARESIS HEMIATHETOSIS SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hhhh syndrome", "shortest_name_length": 13}
{"curie": "UMLS:C5239506", "names": ["Locally Advanced Merkel Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Merkel Cell Carcinoma", "shortest_name_length": 38}
{"curie": "UMLS:C1511321", "names": ["Breast Myoid Hamartoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Myoid Hamartoma", "shortest_name_length": 22}
{"curie": "MONDO:0005281", "names": ["Cholecystosis", "BILIARY DISEASE", "biliary disease", "disease biliary", "biliary diseases", "DISEASE GALLBLADDER", "Gallbladder Disease", "Disease gallbladder", "Gallbladder disease", "GALLBLADDER DISEASE", "gallbladder disease", "Gallbladder Disorder", "gallbladder disorder", "Gallbladder disorder", "gallbladder diseases", "Gallbladder Diseases", "Disease, Gallbladder", "Gall Bladder Disease", "gall bladder disease", "Bladder Disease, Gall", "Gallbladder--Diseases", "GALL BLADDER DISORDER", "Gall bladder disorder", "Disease, Gall Bladder", "Gallbladder disorders", "Gall Bladder Diseases", "gall bladder diseases", "gall bladder disorder", "Gall Bladder Disorder", "Diseases, Gallbladder", "gallbladder disorders", "Diseases, Gall Bladder", "Disease of gallbladder", "Bladder Diseases, Gall", "disease of gall bladder", "Gallbladder disease NOS", "Disorder of gallbladder", "Gallbladder disorder NOS", "disorder of gall bladder", "Gallbladder disorder, NOS", "Disease of gallbladder, NOS", "gallbladder disease (diagnosis)", "gall bladder disease or disorder", "disease (or disorder); gallbladder", "Disorder of gallbladder (disorder)", "disease or disorder of gall bladder", "Unspecified disorder of gallbladder", "Disease of gallbladder, unspecified", "Diseases and Syndromes of Gallbladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gallbladder disorder", "shortest_name_length": 13}
{"curie": "MONDO:0006022", "names": ["acidosis", "acidoses", "ACIDOSIS", "Acidosis", "Acidoses", "Acidosis NOS", "Acidosis, NOS", "acidosis disorder", "Acidosis (disorder)", "acidosis (diagnosis)", "Acidosis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acidosis disorder", "shortest_name_length": 8}
{"curie": "UMLS:C4288409", "names": ["Perforin Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perforin Deficiency", "shortest_name_length": 19}
{"curie": "UMLS:C1560030", "names": ["Deep Connective Tissue Fibrosis", "Fibrosis deep connective tissue", "fibrosis of deep connective tissue", "fibrosis of deep connective tissue (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fibrosis deep connective tissue", "shortest_name_length": 31}
{"curie": "MONDO:0012481", "names": ["MKD", "MVA", "MEVA", "HIDS", "Mevalonicaciduria", "MEVALONIC ACIDURIA", "Mevalonic Aciduria", "Mevalonicacidurias", "mevalonic aciduria", "Mevalonic aciduria", "Aciduria, Mevalonic", "Mevalonate kinase deficiency", "Mevalonate Kinase Deficiency", "Mevalonic aciduria (disorder)", "Kinase Deficiency, Mevalonate", "Mevalonate Kinase Deficiencies", "Kinase Deficiencies, Mevalonate", "Deficiency of mevalonate kinase", "complete mevalonate kinase deficiency", "Complete mevalonate kinase deficiency", "Deficiency of mevalonate kinase (disorder)", "hyperimmunoglobulin D with periodic fever syndrome", "Hyperimmunoglobulin D with Periodic Fever Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mevalonic aciduria", "shortest_name_length": 3}
{"curie": "UMLS:C1334594", "names": ["Malignant Intracranial Neoplasm by Morphology"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Intracranial Neoplasm by Morphology", "shortest_name_length": 45}
{"curie": "UMLS:C1332229", "names": ["Alcohol-Related Laryngeal Carcinoma", "Alcohol-Related Laryngeal Throat Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alcohol-Related Laryngeal Carcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C1142567", "names": ["Joint abscess", "joint; abscess", "abscess; joint"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joint abscess", "shortest_name_length": 13}
{"curie": "MONDO:0010790", "names": ["merrf", "MERRF", "MERRF syndrome", "merrf syndrome", "MERRF SYNDROME", "MERRF Syndrome", "Syndrome, MERRF", "Fukuhara Disease", "Fukuhara syndrome", "Fukuhara Syndrome", "Syndrome, Fukuhara", "epilepsy fiber myoclonic ragged red", "epilepsy fibers myoclonus ragged red", "epilepsy fibres myoclonic ragged red", "epilepsy fibers myoclonic ragged red", "Myoclonic epilepsy - ragged red fibers", "myoclonic epilepsy - ragged red fibers", "Myoclonic epilepsy - ragged red fibres", "Myoclonic epilepsy and ragged-red fibers", "Myoclonus epilepsy AND ragged red fibers", "Myoclonic epilepsy and ragged-red fibres", "Myoclonus epilepsy and ragged red fibers", "Myoclonic Epilepsy and Ragged Red Fibers", "myoclonus epilepsy and ragged red fibers", "myoclonic epilepsy with ragged red fibers", "Myoclonic Epilepsy with Ragged Red Fibers", "Myoclonic epilepsy with ragged red fibers", "Myoclonic Epilepsy with Ragged-Red Fibers", "Myoclonic epilepsy with ragged red fibres", "Myoencephalopathy Ragged-Red Fiber Disease", "myoencephalopathy ragged-red fiber disease", "Myoencephalopathy Ragged Red Fiber Disease", "MERRF - Myoclonic epilepsy - ragged red fibers", "Myoclonus with Epilepsy with Ragged Red Fibers", "MERRF - Myoclonic epilepsy - ragged red fibres", "MERFF - myoclonic epilepsy with ragged red fibres", "MERFF - myoclonic epilepsy with ragged red fibers", "Myoclonus with epilepsy and with Ragged Red Fibers", "myoclonus with epilepsy and with ragged Red fibers", "MYOCLONIC EPILEPSY ASSOCIATED WITH RAGGED-RED FIBERS", "Myoclonus epilepsy associated with ragged-red fibres", "Myoclonic epilepsy with ragged red fibers (disorder)", "myoclonus epilepsy associated with ragged-red fibres", "Myoclonic Epilepsy Associated with Ragged-Red Fibers", "myoclonic epilepsy associated with ragged-RED fibers", "myoclonic epilepsy associated with ragged red fibers", "Myoclonic Epilepsy Associated with Ragged Red Fibers", "Myoclonic epilepsy associated with ragged-red fibers", "myoclonic epilepsy and ragged red fibers (MERRF) syndrome", "Myoclonus with Epilepsy and with Ragged Red Fibers (MERRF syndrome)", "myoclonus with epilepsy and with ragged Red fibers (MERRF syndrome)", "myoclonic epilepsy and ragged red fibers (MERRF) syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MERRF syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0017640", "names": ["Cyanide-induced parkinsonism", "cyanide-induced parkinsonism", "Parkinsonism caused by cyanide", "Cyanide-induced parkinsonism-dystonia", "Parkinsonism caused by cyanide (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cyanide-induced parkinsonism", "shortest_name_length": 28}
{"curie": "MONDO:0016588", "names": ["Feer", "Swift", "acrodynia", "ACRODYNIA", "Acrodynia", "erythredema", "DISEASE PINK", "Feer disease", "Pink Disease", "pink disease", "Feer Disease", "Disease pink", "Pink disease", "feer disease", "swift disease", "pink; disease", "disease; pink", "Swift disease", "Feers Disease", "disease pinks", "Swift Disease", "Swifts Disease", "Feer's disease", "swifts disease", "feer's disease", "Feer's Disease", "Swift's Disease", "swift's disease", "Selter's disease", "Swift-Feer disease", "Acrodynic Erythema", "Erythema, Acrodynic", "infantile acrodynia", "Bilderbeck's disease", "Acrodynia due to mercury", "erythroedema polyneuritis", "erythredema; polyneuritic", "polyneuropathy erythredema", "Erythredema polyneuropathy", "Acrodynia caused by mercury", "Erythroedema polyneuropathy", "infantile mercury poisoning", "infantile mercury intoxication", "Chronic Childhood Mercurialism", "Mercurialism, Chronic Childhood", "Childhood Mercurialism, Chronic", "Chronic Childhood Mercurialisms", "Childhood Mercurialisms, Chronic", "Acrodynia due to mercury poisoning", "Acrodynia caused by mercury poisoning", "Acrodynia due to mercury poisoning (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile mercury poisoning", "shortest_name_length": 4}
{"curie": "UMLS:C3203690", "names": ["Oligocholia", "Deficiency of bile secretion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Deficiency of bile secretion", "shortest_name_length": 11}
{"curie": "MONDO:0025713", "names": ["HAE7", "angioedema, hereditary, 7", "ANGIOEDEMA, HEREDITARY, 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angioedema, hereditary, 7", "shortest_name_length": 4}
{"curie": "UMLS:C1336924", "names": ["AIDS-Related Cervical Kaposi Sarcoma", "AIDS-Related Cervical Kaposi's Sarcoma", "AIDS-Related Kaposi's Sarcoma of Cervix", "AIDS-Related Kaposi's Sarcoma of the Cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Cervical Kaposi Sarcoma", "shortest_name_length": 36}
{"curie": "MONDO:0021455", "names": ["Benign Neck Tumor", "benign tumor neck", "neck benign tumor", "benign neck tumor", "benign neck tumors", "Benign tumor of neck", "Benign Tumor of Neck", "neck benign neoplasm", "Benign Neck Neoplasm", "benign tumor of neck", "benign neck neoplasm", "Benign tumour of neck", "Benign Neoplasm of Neck", "benign neoplasm of neck", "Benign neoplasm of neck", "Benign Tumor of the Neck", "benign tumor of the neck", "Benign Neoplasm of the Neck", "benign neoplasm of the neck", "Benign neoplasm of neck, NOS", "Benign neoplasm of neck (disorder)", "benign neoplasm of neck (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of neck", "shortest_name_length": 17}
{"curie": "MONDO:0010943", "names": ["SCZD4", "SCHIZOPHRENIA 4", "schizophrenia 4", "schizophrenia type 4", "schizophrenia, susceptibility to, 4", "SCHIZOPHRENIA SUSCEPTIBILITY LOCUS, CHROMOSOME 22q11-RELATED", "schizophrenia susceptibility locus, chromosome 22Q11-related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schizophrenia 4", "shortest_name_length": 5}
{"curie": "UMLS:C0021280", "names": ["infant nutrition disorder", "Infant Nutrition Disorder", "Infant Nutrition Disorders", "Nutrition Disorder, Infant", "Nutrition Disorders, Infant", "Nutrition disorders in infants"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infant Nutrition Disorders", "shortest_name_length": 25}
{"curie": "MONDO:0016495", "names": ["functional variant of GBS", "functional variant of Guillain-Barre syndrome", "functional variant of Guillain-Barré syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "functional variant of Guillain-Barre syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0014497", "names": ["PEPNS", "polyendocrine-polyneuropathy syndrome", "POLYENDOCRINE-POLYNEUROPATHY SYNDROME", "Polyendocrine-polyneuropathy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyendocrine-polyneuropathy syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0333291", "names": ["ulcer bleed", "bleed ulcer", "bleeds ulcers", "Ulcer bleeding", "Bleeding ulcer", "bleeding ulcer", "ulcer bleeding", "ulcer; bleeding", "bleeding ulcers", "Ulcer hemorrhage", "ulcer; hemorrhage", "Hemorrhagic ulcer", "Ulcer haemorrhage", "hemorrhage; ulcer", "Haemorrhagic ulcer", "Ulcer hemorrhage NOS", "Ulcer haemorrhage NOS", "Bleeding ulcer (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bleeding ulcer", "shortest_name_length": 11}
{"curie": "MONDO:0010690", "names": ["NBM1", "NBMI", "CSNB1A", "nyctalopia", "Hemeralopia-myopia", "HEMERALOPIA-MYOPIA", "hemeralopia-myopia", "Myopia-night blindness", "complete CSNB X-linked", "myopia-night blindness", "MYOPIA-NIGHT BLINDNESS", "CSNB, complete, X-linked", "CSNB, COMPLETE, X-LINKED", "CSNB, Complete, X-Linked", "congenital stationary night blindness 1A", "NYX congenital stationary night blindness", "congenital stationary night blindness type 1A", "NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A", "Night Blindness, Congenital Stationary, Type 1A", "congenital stationary night blindness - type 1a", "night blindness, congenital stationary, type 1A", "congenital stationary night blindness 1A X-linked", "congenital stationary night blindness with myopia", "NYX-related congenital stationary night blindness", "NIGHT BLINDNESS, CONGENITAL STATIONARY, WITH MYOPIA", "Night blindness, congenital stationary, with myopia", "night blindness, congenital stationary, with myopia", "congenital stationary night blindness - type 1a (diagnosis)", "congenital stationary night blindness caused by mutation in NYX", "night blindness, congenital stationary (complete), 1A, X-linked, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital stationary night blindness 1A", "shortest_name_length": 4}
{"curie": "MONDO:0014984", "names": ["LICS", "lung disease, immunodeficiency, and chromosome breakage syndrome", "LUNG DISEASE, IMMUNODEFICIENCY, AND CHROMOSOME BREAKAGE SYNDROME", "lung disease, immunodeficiency, and chromosome breakage syndrome;"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung disease, immunodeficiency, and chromosome breakage syndrome;", "shortest_name_length": 4}
{"curie": "UMLS:C2981344", "names": ["Stage I Lung Cancer", "Stage I Lung Cancer AJCC v6", "Stage I Lung Carcinoma AJCC v6", "Stage I Carcinoma of Lung AJCC v6", "Stage I Carcinoma of the Lung AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Lung Cancer AJCC v6", "shortest_name_length": 19}
{"curie": "UMLS:C1708193", "names": ["Gastric Diverticulitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Diverticulitis", "shortest_name_length": 22}
{"curie": "UMLS:C3640961", "names": ["Stage 2A Neuroblastoma", "Stage IIA Neuroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 2A Neuroblastoma", "shortest_name_length": 22}
{"curie": "MONDO:0100382", "names": ["DEK-NUP214", "AML, t(6;9)(p23;q34)", "AML, t(6;9)(p22;q34)", "AML, t(6;9)(p23;q34.1)", "AML, t(6;9)(p22.3;q34.1)", "Acute Myeloid Leukemia with t(6;9)", "AML with t(6;9)(p23;q34);DEK-NUP214", "AML with t(6;9)(p23;q34); DEK-NUP214", "AML with t(6;9)(p23;q34.1);DEK-NUP214", "acute myeloid leukemia, t(6;9)(p23;q34.1)", "acute myeloid leukemia with t(6;9)(p23;q34)", "acute myeloid leukemia with t(6;9) (p23;q34.1)", "Acute myeloid leukemia with t(6;9)(p23;q34); DEK-NUP214", "Acute Myeloid Leukemia with t(6;9)(p23;q34); DEK-NUP214", "Acute myeloid leukaemia with t(6;9)(p23;q34); DEK-NUP214", "Acute Myeloid Leukemia with t(6;9) (p23;q34.1); DEK-NUP214", "Acute myeloid leukemia with t(6;9)(p23;q34); DEK-NUP214 (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, t(6;9)(p23;q34.1)", "shortest_name_length": 10}
{"curie": "UMLS:C5203858", "names": ["Usual Prostate Adenocarcinoma with Neuroendocrine Cells", "Usual Prostate Adenocarcinoma with Neuroendocrine Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Usual Prostate Adenocarcinoma with Neuroendocrine Differentiation", "shortest_name_length": 55}
{"curie": "MONDO:0014296", "names": ["WARBM4", "Micro Syndrome 4", "micro syndrome 4", "WARBURG MICRO SYNDROME 4", "Warburg micro syndrome 4", "WARBURG micro syndrome 4", "Warburg micro syndrome type 4", "TBC1D20 Warburg micro syndrome", "Warburg micro syndrome caused by mutation in TBC1D20"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Warburg micro syndrome 4", "shortest_name_length": 6}
{"curie": "UMLS:C0022744", "names": ["Knee injury", "injury knee", "knee injury", "Injury;knee", "KNEE INJURY", "Knee Injury", "injury knees", "Injury, Knee", "injury; knee", "knee; injury", "knee injuries", "injuries knee", "Knee Injuries", "Injuries, Knee", "injuries knees", "Injury of knee", "injury of knee", "Injury of knee (disorder)", "injury of knee (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Knee Injuries", "shortest_name_length": 11}
{"curie": "MONDO:0011375", "names": ["Brittle Bone Disorder", "brittle bone disorder", "BRITTLE BONE DISORDER"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brittle bone disorder", "shortest_name_length": 21}
{"curie": "MONDO:0011741", "names": ["HSCR6", "Hirschsprung disease, susceptibility to, 6", "HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hirschsprung disease, susceptibility to, 6", "shortest_name_length": 5}
{"curie": "MONDO:0011525", "names": ["CNC2", "Carney complex type 2", "Carney Complex, Type 2", "CARNEY COMPLEX, TYPE 2", "Carney complex, type 2", "Carney complex, type II", "Carney Complex, Type II", "CARNEY MYXOMA-ENDOCRINE COMPLEX, TYPE 2", "Carney Myxoma-endocrine Complex, type 2", "Carney Myxoma-Endocrine Complex, Type II", "Carney Myxoma Endocrine Complex, Type II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carney complex type 2", "shortest_name_length": 4}
{"curie": "MONDO:0009573", "names": ["Megaepiphyseal dwarfism", "MEGAEPIPHYSEAL DWARFISM", "megaepiphyseal dwarfism", "Mega-epiphyseal dwarfism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "megaepiphyseal dwarfism", "shortest_name_length": 23}
{"curie": "UMLS:C0268064", "names": ["Transfusion Hemosiderosis", "Transfusion hemosiderosis", "hemosiderosis; transfusion", "transfusion; hemosiderosis", "Transfusion haemosiderosis", "Transfusion Hemochromatosis", "Transfusion induced iron overload", "Transfusion hemosiderosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transfusion hemosiderosis", "shortest_name_length": 25}
{"curie": "MONDO:0700023", "names": ["chromosome 16 disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 16 disorder", "shortest_name_length": 22}
{"curie": "UMLS:C0521509", "names": ["Injection site induration", "Injection site induration (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site induration", "shortest_name_length": 25}
{"curie": "MONDO:0008731", "names": ["familial adrenal hypoplasia, miniature type", "familial adrenal hypoplasia with absent pituitary LH", "familial adrenal hypoplasia with absent pituitary luteinizing hormone", "ADRENAL HYPOPLASIA, CONGENITAL, WITH ABSENT PITUITARY LUTEINIZING HORMONE", "Adrenal Hypoplasia, Congenital, With Absent Pituitary Luteinizing Hormone", "adrenal hypoplasia, congenital, with absent pituitary luteinizing hormone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial adrenal hypoplasia with absent pituitary luteinizing hormone", "shortest_name_length": 43}
{"curie": "UMLS:C5418958", "names": ["Unresectable Primary Peritoneal Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Primary Peritoneal Serous Adenocarcinoma", "shortest_name_length": 53}
{"curie": "UMLS:C5204991", "names": ["Carcinoma Arising in Bladder Diverticulum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carcinoma Arising in Bladder Diverticulum", "shortest_name_length": 41}
{"curie": "MONDO:0011452", "names": ["AH", "Lah2", "LAH2", "HYPT7", "Hypt7", "ARWH2", "WH/HT", "Wh/Ht", "HYPOTRICHOSIS 7", "hypotrichosis 7", "LIPH hypotrichosis", "hypotrichosis type 7", "Total Hypotrichosis, Mari type", "total Mari type hypotrichosis,", "total hypotrichosis, Mari type", "hypotrichosis, total, Mari type", "HYPOTRICHOSIS, TOTAL, MARI TYPE", "Hypotrichosis, Total, Mari Type", "HYPOTRICHOSIS, AUTOSOMAL RECESSIVE", "Hypotrichosis, Autosomal Recessive", "hypotrichosis, autosomal recessive", "hypotrichosis caused by mutation in LIPH", "Mari type Alopecia universalis congenita", "Mari type alopecia universalis congenita", "Alopecia Universalis Congenita, Mari type", "alopecia universalis congenita, Mari type", "hypotrichosis, localized, autosomal recessive 2", "HYPOTRICHOSIS, LOCALIZED, AUTOSOMAL RECESSIVE 2", "Hypotrichosis, Localized, Autosomal Recessive, 2", "woolly hair, autosomal recessive 2 with or without hypotrichosis", "woolly hair, autosomal recessive 2, with or without hypotrichosis", "WOOLLY HAIR, AUTOSOMAL RECESSIVE 2, WITH OR WITHOUT HYPOTRICHOSIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotrichosis 7", "shortest_name_length": 2}
{"curie": "MONDO:0017627", "names": ["congenital hereditary facial palsy with variable deafness", "Congenital hereditary facial palsy with variable deafness", "Congenital hereditary facial palsy with variable hearing loss", "congenital hereditary facial palsy with variable hearing loss", "Congenital hereditary facial paralysis with variable deafness", "congenital hereditary facial paralysis with variable deafness", "Congenital hereditary facial paralysis-variable deafness syndrome", "congenital hereditary facial paralysis-variable deafness syndrome", "Congenital hereditary facial paralysis-variable hearing loss syndrome", "congenital hereditary facial paralysis-variable hearing loss syndrome", "Congenital hereditary facial paralysis with variable hearing loss syndrome", "Congenital hereditary facial paralysis with variable hearing loss syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital hereditary facial paralysis-variable hearing loss syndrome", "shortest_name_length": 57}
{"curie": "MONDO:0001242", "names": ["DIC in newborn", "Newborn defibrination syndrome", "Defibrination syndrome of newborn", "Newborn disseminated intravascular coagulation", "Neonatal Disseminated Intravascular Coagulation", "neonatal disseminated intravascular coagulation", "Disseminated Intravascular Coagulation in Newborn", "Disseminated intravascular coagulation in newborn", "Disseminated intravascular coagulation of newborn", "disseminated intravascular coagulation in newborn", "neonatal disseminated intravascular coagulation (diagnosis)", "Disseminated intravascular coagulation of fetus and newborn", "Disseminated intravascular coagulation in newborn (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disseminated intravascular coagulation in newborn", "shortest_name_length": 14}
{"curie": "UMLS:C5420297", "names": ["Testicular Sarcomatoid Mesothelioma", "Paratesticular Sarcomatoid Mesothelioma", "Tunica Vaginalis Sarcomatoid Mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paratesticular Sarcomatoid Mesothelioma", "shortest_name_length": 35}
{"curie": "MONDO:0016950", "names": ["partial trisomy of chromosome 17p", "partial duplication of chromosome 17p", "partial trisomy of the short arm of chromosome 17", "partial duplication of the short arm of chromosome 17", "partial duplication of the short arm of chromosome type 17"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of the short arm of chromosome 17", "shortest_name_length": 33}
{"curie": "UMLS:C4553846", "names": ["IV", "Stage IV Thyroid Gland Papillary Cancer", "Stage IV Thyroid Gland Papillary Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Thyroid Gland Papillary Carcinoma AJCC v8", "shortest_name_length": 2}
{"curie": "MONDO:0010900", "names": ["Woods Leversha Rogers syndrome", "intrauterine growth retardation with increased mitomycin c sensitivity", "Intrauterine Growth Retardation with Increased Mitomycin C Sensitivity", "INTRAUTERINE GROWTH RETARDATION WITH INCREASED MITOMYCIN C SENSITIVITY", "Severe intrauterine growth retardation with increased mitomycin C sensitivity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intrauterine growth retardation with increased mitomycin c sensitivity", "shortest_name_length": 30}
{"curie": "UMLS:C1266098", "names": ["Branchial Anlage Mixed Tumor", "Ectopic Hamartomatous Thymoma", "Ectopic hamartomatous thymoma", "Ectopic hamartomatous thymoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ectopic hamartomatous thymoma", "shortest_name_length": 28}
{"curie": "MONDO:0003641", "names": ["CNS Hematopoietic Tumor", "CNS hematopoietic tumor", "CNS hematopoietic neoplasm", "CNS Hematopoietic Neoplasm", "Hematopoietic Neoplasm of CNS", "hematopoietic neoplasm of CNS", "Hematopoietic Neoplasm of the CNS", "hematopoietic neoplasm of the CNS", "central nervous system hematologic cancer", "central nervous system hematopoietic tumor", "Lymphomas and Hemopoietic Neoplasms of CNS", "Central Nervous System Hematopoietic Tumor", "lymphomas and hemopoietic neoplasms of CNS", "Central Nervous System Hematopoietic Neoplasm", "central nervous system hematopoietic neoplasm", "hematopoietic tumor of central nervous system", "Hematopoietic Tumor of Central Nervous System", "central nervous system hematopoietic neoplasms", "Central Nervous System Hematopoietic Neoplasms", "lymphomas and hemopoietic neoplasms of the CNS", "Lymphomas and Hemopoietic Neoplasms of the CNS", "Hematopoietic Neoplasm of Central Nervous System", "hematopoietic neoplasm of central nervous system", "Hematopoietic Tumor of the Central Nervous System", "hematopoietic tumor of the central nervous system", "Hematopoietic Neoplasm of the Central Nervous System", "hematopoietic neoplasm of the central nervous system", "central nervous system hematopoietic and lymphoid system neoplasm", "hematopoietic and lymphoid system neoplasm of central nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system hematopoietic neoplasm", "shortest_name_length": 23}
{"curie": "MONDO:0008069", "names": ["Leigh syndrome, adult", "LEIGH SYNDROME, ADULT", "Leigh Syndrome, Adult", "necrotizing encephalomyelopathy, subacute, of Leigh, adult", "NECROTIZING ENCEPHALOMYELOPATHY, SUBACUTE, OF LEIGH, ADULT", "Necrotizing Encephalomyelopathy, Subacute, of Leigh, Adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "necrotizing encephalomyelopathy, subacute, of Leigh, adult", "shortest_name_length": 21}
{"curie": "MONDO:0000565", "names": ["Endocarditis infective", "endocarditis infective", "Infective endocarditis", "infective endocarditis", "Infective Endocarditis", "Bacterial endocarditis", "Endocarditis, Infective", "endocarditis, infective", "Infectious endocarditis", "Infective Endocarditides", "Endocarditides, Infective", "IE - Infective endocarditis", "Infective endocarditis (disorder)", "infective endocarditis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infective endocarditis", "shortest_name_length": 22}
{"curie": "UMLS:C0751182", "names": ["Occipital Trauma", "Occipital Traumas", "Trauma, Occipital", "Traumas, Occipital", "Occipital Region Trauma", "Occipital Region Traumas", "Trauma, Occipital Region", "Region Trauma, Occipital", "Region Traumas, Occipital", "Traumas, Occipital Region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Occipital Region Trauma", "shortest_name_length": 16}
{"curie": "UMLS:C1333606", "names": ["Femoropopliteal Occlusive Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Femoropopliteal Occlusive Disease", "shortest_name_length": 33}
{"curie": "MONDO:0009953", "names": ["RHS", "LAD2", "CDG2C", "lad-II", "CDG 2C", "CDGIIc", "LAD-II", "CDG IIc", "CDG-IIc", "SLC35C1-CDG", "lad-type II", "LAD-Type II", "SLC35C1-CDG (CDG-IIc)", "sialyl-Lewis X defect", "Sialyl-Lewis X Defect", "CDG syndrome type IIc", "Sialyl-Lewis X defect", "Rambam-Hasharon syndrome", "Rambam-Hasharon Syndrome", "RAMBAM-HASHARON SYNDROME", "Rambam Hasharon syndrome", "leukocyte adhesion deficiency 2", "leukocyte adhesion defect - type II", "Leukocyte Adhesion Deficiency Type 2", "leukocyte adhesion deficiency type 2", "Leukocyte adhesion deficiency type II", "Leukocyte adhesion deficiency, type 2", "leukocyte adhesion deficiency, type 2", "leukocyte adhesion deficiency type II", "leukocyte adhesion deficiency, type II", "Leucocyte adhesion deficiency - type 2", "Leukocyte adhesion deficiency - type 2", "LEUKOCYTE ADHESION DEFICIENCY, TYPE II", "Leukocyte Adhesion Deficiency, Type II", "LAD - Leukocyte adhesion deficiency type 2", "LAD - Leucocyte adhesion deficiency type 2", "Congenital disorder of glycosylation type IIc", "Congenital disorder of glycosylation, type 2C", "congenital disorder of glycosylation type IIC", "congenital disorder of glycosylation type IIc", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc", "Congenital Disorder Of Glycosylation, Type IIC", "congenital disorder of glycosylation, type IIc", "leukocyte adhesion defect - type II (diagnosis)", "Leucocyte adhesion molecule deficiency - type 2", "Leukocyte adhesion molecule deficiency - type 2", "Leukocyte adhesion deficiency - type 2 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukocyte adhesion deficiency type II", "shortest_name_length": 3}
{"curie": "MONDO:0012528", "names": ["HH4", "KAL4", "Kallman syndrome 4", "Kallmann syndrome 4", "Kallmann Syndrome 4", "PROK2 hypogonadotropic hypogonadism", "HYPOGONADOTROPIC HYPOGONADISM 4 WITH OR WITHOUT ANOSMIA", "hypogonadotropic hypogonadism 4 with or without anosmia", "hypogonadotropic hypogonadism caused by mutation in PROK2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadotropic hypogonadism 4 with or without anosmia", "shortest_name_length": 3}
{"curie": "UMLS:C4725598", "names": ["Gastric Cardia Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Cardia Squamous Cell Carcinoma", "shortest_name_length": 38}
{"curie": "UMLS:C0278880", "names": ["stage I melanoma", "melanoma, stage I", "stage I cutaneous melanoma", "melanoma, cutaneous stage I", "cutaneous melanoma, stage I", "Stage I Melanoma of Skin AJCC v6", "Stage I Cutaneous (Skin) Melanoma", "Stage I Cutaneous Melanoma AJCC v6", "Stage I Melanoma of the Skin AJCC v6", "Stage I Malignant Skin Melanoma AJCC v6", "Stage I Malignant Melanoma of Skin AJCC v6", "Stage I Malignant Cutaneous Melanoma AJCC v6", "Malignant Melanoma (of Skin), Stage I AJCC v6", "Stage I Malignant Melanoma of the Skin AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Cutaneous Melanoma AJCC v6", "shortest_name_length": 16}
{"curie": "MONDO:0009570", "names": ["McDonough syndrome", "MCDONOUGH SYNDROME", "McDonough syndrome (disorder)", "McDonough syndrome (diagnosis)", "Mental retardation, peculiar facies, kyphoscoliosis, diastasis recti, cryptorchidism, and congenital heart defect", "mental retardation, peculiar facies, kyphoscoliosis, diastasis recti, cryptorchidism, and congenital heart defect", "intellectual disability, peculiar facies, kyphoscoliosis, diastasis recti, cryptorchidism, and congenital heart defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "McDonough syndrome", "shortest_name_length": 18}
{"curie": "MONDO:0054842", "names": ["PKD6", "DNAJB11 polycystic kidney disease", "polycystic kidney disease caused by mutation in DNAJB11", "POLYCYSTIC KIDNEY DISEASE 6 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE", "polycystic kidney disease 6 with or without polycystic liver disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polycystic kidney disease 6 with or without polycystic liver disease", "shortest_name_length": 4}
{"curie": "MONDO:0004933", "names": ["HLHS", "hypoplasia left heart", "HYPOPLASTIC LEFT HEART", "hypoplastic left heart", "left hypoplastic heart", "left heart hypoplastic", "heart hypoplastic left", "Hypoplastic left heart", "Hypoplasia of left heart", "Underdeveloped left heart", "Rudimentary left ventricle", "Left ventricular hypoplasia", "Left Heart Hypoplasia Syndrome", "Hypoplastic left heart syndrome", "Hypoplastic Left Heart Syndrome", "Heart left ventricle hypoplasia", "left heart syndrome; hypoplasia", "hypoplasia; left heart syndrome", "hypoplastic left heart syndrome", "heart hypoplastic left syndrome", "HYPOPLASTIC LEFT HEART SYNDROME", "Left Heart Syndrome, Hypoplastic", "hypoplastic left-heart; syndrome", "syndrome; hypoplastic left-heart", "syndrome; heart, hypoplastic left", "HLH - Hypoplastic left heart syndrome", "Left ventricular hypoplasia (disorder)", "HLHS - Hypoplastic left heart syndrome", "heart; hypoplasia, left heart syndrome", "hypoplasia; heart, left heart syndrome", "heart; hypoplasia, left heart (syndrome)", "hypoplasia; heart, left heart (syndrome)", "Hypoplastic left heart syndrome (disorder)", "hypoplastic left heart syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypoplastic left heart syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0002747", "names": ["uterine mucinous carcinoma", "Endometrial Mucinous Adenocarcinoma", "endometrium mucinous adenocarcinoma", "endometrial mucinous adenocarcinoma", "uterine Corpus mucinous adenocarcinoma", "Uterine Corpus Mucinous Adenocarcinoma", "uterine corpus mucinous adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometrial mucinous adenocarcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0014273", "names": ["MRT40", "NEDFCF", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 40", "mental retardation, autosomal recessive 40", "intellectual disability, autosomal recessive 40", "mental retardation, autosomal recessive type 40", "intellectual disability, autosomal recessive type 40", "autosomal recessive intellectual developmental disorder 40", "intellectual developmental disorder, autosomal recessive 40", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 40", "microcephaly-thin corpus callosum-intellectual disability syndrome", "NEURODEVELOPMENTAL DISORDER WITH FEEDING DIFFICULTIES, THIN CORPUS CALLOSUM, AND FOOT DEFORMITY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly-thin corpus callosum-intellectual disability syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0016080", "names": ["congenital bronchobiliary fistula", "Congenital bronchobiliary fistula", "Congenital bronchobiliary fistula (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital bronchobiliary fistula", "shortest_name_length": 33}
{"curie": "MONDO:0016034", "names": ["Tessier cleft number 1,2", "cleft lip with or without cleft palate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleft lip with or without cleft palate", "shortest_name_length": 24}
{"curie": "MONDO:0019913", "names": ["UPD(7)mat", "silver-Russell syndrome due to maternal uniparental disomy of chromosome 7", "Silver-Russell syndrome due to maternal uniparental disomy of chromosome type 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "silver-Russell syndrome due to maternal uniparental disomy of chromosome 7", "shortest_name_length": 9}
{"curie": "MONDO:0001263", "names": ["ocular histoplasmosis", "Retinitis histoplasma", "retinitis histoplasmosis", "histoplasmosis retinitis", "Histoplasmosis retinitis", "Histoplasmosis with retinitis", "histoplasmosis with retinitis", "Histoplasma capsulatum retinitis", "ocular histoplasmosis (diagnosis)", "Histoplasmosis, unspecified, retinitis", "Histoplasma capsulatum caused retinitis", "Histoplasmosis with retinitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "histoplasmosis retinitis", "shortest_name_length": 21}
{"curie": "MONDO:0003687", "names": ["endocardium cancer", "cancer of endocardium", "malignant Endocardial tumor", "Malignant Endocardial Tumor", "malignant endocardial tumor", "malignant endocardial neoplasm", "Malignant Endocardial Neoplasm", "Malignant Tumor of Endocardium", "malignant endocardium neoplasm", "malignant tumor of endocardium", "Malignant tumor of endocardium", "Malignant tumour of endocardium", "Malignant Neoplasm of Endocardium", "Malignant neoplasm of endocardium", "malignant neoplasm of endocardium", "malignant tumor of the endocardium", "Malignant Tumor of the Endocardium", "Malignant Neoplasm of the Endocardium", "malignant neoplasm of the endocardium", "Malignant tumor of endocardium (disorder)", "malignant neoplasm of endocardium (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endocardium cancer", "shortest_name_length": 18}
{"curie": "MONDO:0017829", "names": ["AD pRTA", "autosomal dominant proximal renal tubular acidosis", "proximal renal tubular acidosis, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant proximal renal tubular acidosis", "shortest_name_length": 7}
{"curie": "MONDO:0016781", "names": ["maternal del(14)(q32.2)", "maternal monosomy 14q32.2", "maternal 14q32.2 microdeletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maternal 14q32.2 microdeletion syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0100194", "names": ["pregnancy associated osteoporosis", "pregnancy and lactation-associated osteoporosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pregnancy associated osteoporosis", "shortest_name_length": 33}
{"curie": "MONDO:0007131", "names": ["Anonychia with flexural pigmentation", "ANONYCHIA WITH FLEXURAL PIGMENTATION", "anonychia with flexural pigmentation", "Anonychia with Flexural Pigmentation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anonychia with flexural pigmentation", "shortest_name_length": 36}
{"curie": "MONDO:0014193", "names": ["CILD23", "primary ciliary dyskinesia 23", "CILIARY DYSKINESIA, PRIMARY, 23", "ciliary dyskinesia, primary, 23", "ARMC4 primary ciliary dyskinesia", "primary ciliary dyskinesia type 23", "ciliary dyskinesia, primary, type 23", "primary ciliary dyskinesia caused by mutation in ARMC4", "primary ciliary dyskinesia 23 with or without situs inversus", "ciliary dyskinesia, primary, 23, with or without situs inversus", "CILIARY DYSKINESIA, PRIMARY, 23, WITH OR WITHOUT SITUS INVERSUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia 23", "shortest_name_length": 6}
{"curie": "UMLS:C2242494", "names": ["Hemorrhagic erosive gastritis", "Haemorrhagic erosive gastritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemorrhagic erosive gastritis", "shortest_name_length": 29}
{"curie": "UMLS:C5204619", "names": ["Bladder Solitary Fibrous Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder Solitary Fibrous Tumor", "shortest_name_length": 30}
{"curie": "MONDO:0022293", "names": ["Penis vascular disorder", "Penile Vascular Disorder", "penile vascular disorder", "Penile vascular disorder", "Vascular disorder of penis", "vascular disorder of penis", "Vascular disorders of penis", "Vascular disorder of penis (disorder)", "vascular disorder of penis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vascular disorder of penis", "shortest_name_length": 23}
{"curie": "UMLS:C3887519", "names": ["childhood cerebral neuroblastoma", "Childhood Cerebral Neuroblastoma", "pediatric cerebral neuroblastoma", "cerebral neuroblastoma, pediatric", "cerebral neuroblastoma, childhood", "neuroblastoma, childhood cerebral", "neuroblastoma, pediatric cerebral", "neuroblastoma, cerebral, childhood", "neuroblastoma, cerebral, pediatric", "Central Nervous System Neuroblastoma", "Childhood Central Nervous System Neuroblastoma", "childhood central nervous system neuroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Central Nervous System Neuroblastoma", "shortest_name_length": 32}
{"curie": "MONDO:0009599", "names": ["metaphyseal dysostosis mental retardation conductive deafness", "metaphyseal dysostosis intellectual disability conductive deafness", "Metaphyseal Dysostosis, Mental Retardation, and Conductive Deafness", "metaphyseal dysostosis, mental retardation, and conductive deafness", "METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS", "metaphyseal dysostosis, conductive hearing loss and mental retardation", "metaphyseal dysostosis, intellectual disability, and conductive deafness", "metaphyseal dysostosis, conductive hearing loss and intellectual disability", "metaphyseal dysostosis-intellectual disability-conductive deafness syndrome", "METAPHYSEAL DYSOSTOSIS, IMPAIRED INTELLECTUAL DEVELOPMENT, AND CONDUCTIVE DEAFNESS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metaphyseal dysostosis-intellectual disability-conductive deafness syndrome", "shortest_name_length": 61}
{"curie": "UMLS:C1333603", "names": ["Female Non-Neoplastic Reproductive System Disease", "Female Non-Neoplastic Reproductive System Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Female Non-Neoplastic Reproductive System Disorder", "shortest_name_length": 49}
{"curie": "MONDO:0032721", "names": ["SEDKF", "SED with elevated blood lysosomal enzymes", "Sed With Elevated Blood Lysosomal Enzymes", "SED WITH ELEVATED BLOOD LYSOSOMAL ENZYMES", "spondyloepiphyseal dysplasia Kondo-Fu type", "SPONDYLOEPIPHYSEAL DYSPLASIA, KONDO-FU TYPE", "spondyloepiphyseal dysplasia, kondo-fu type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepiphyseal dysplasia, kondo-fu type", "shortest_name_length": 5}
{"curie": "MONDO:0018811", "names": ["congenital portosystemic shunt", "congenital portosystemic venous fistula"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital portosystemic shunt", "shortest_name_length": 30}
{"curie": "UMLS:C5555294", "names": ["Current_CMV_infection", "Current CMV Infection", "Current HCMV Infection", "Current Cytomegalovirus Infection", "Current Cytomegaloviral Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Current Cytomegalovirus Infection", "shortest_name_length": 21}
{"curie": "MONDO:0008426", "names": ["SGS", "Montefiore syndrome", "Shprintzen-Goldberg Syndrome", "Shprintzen-Goldberg syndrome", "Shprintzen Golberg craniosynostosis", "MARFANOID CRANIOSYNOSTOSIS SYNDROME", "Marfanoid-Craniosynostosis Syndrome", "marfanoid craniosynostosis syndrome", "Marfanoid craniosynostosis syndrome", "Marfanoid-craniosynostosis syndrome", "Shprintzen-Goldberg marfanoid syndrome", "Shprintzen Golberg craniosynostosis syndrome", "Shprintzen Goldberg craniosynostosis syndrome", "SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME", "Shprintzen-Goldberg craniosynostosis syndrome", "Shprintzen-Goldberg Craniosynostosis Syndrome", "Marfanoid disorder with craniosynostosis type 1", "Craniosynostosis and Marfanoid disorder, type 1", "Marfanoid disorder with craniosynostosis, type 1", "MARFANOID DISORDER WITH CRANIOSYNOSTOSIS, TYPE I", "Marfanoid Disorder With Craniosynostosis, Type I", "Shprintzen Goldberg craniosynostosis syndrome (disorder)", "Shprintzen Goldberg craniosynostosis syndrome (diagnosis)", "craniosynostosis-arachnodactyly-abdominal hernia syndrome", "Craniosynostosis with arachnodactyly and abdominal hernias", "CRANIOSYNOSTOSIS WITH ARACHNODACTYLY AND ABDOMINAL HERNIAS", "craniosynostosis with arachnodactyly and abdominal hernias", "congenital malformation syndromes Shprintzen Goldberg craniosynostosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Shprintzen-Goldberg syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0009081", "names": ["deafness, congenital, with total albinism", "DEAFNESS, CONGENITAL, WITH TOTAL ALBINISM", "Deafness, Congenital, with Total Albinism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness, congenital, with total albinism", "shortest_name_length": 41}
{"curie": "MONDO:0018759", "names": ["childhood-onset progressive contractures-limb-girdle weakness-muscle dystrophy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood-onset progressive contractures-limb-girdle weakness-muscle dystrophy syndrome", "shortest_name_length": 87}
{"curie": "MONDO:0020383", "names": ["fundus pulverulentus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fundus pulverulentus", "shortest_name_length": 20}
{"curie": "UMLS:C5421330", "names": ["Chronic Intestinal Cryptosporidiosis", "Cryptosporidiosis, Chronic Intestinal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic Intestinal Cryptosporidiosis", "shortest_name_length": 36}
{"curie": "MONDO:0008255", "names": ["PLATELET FACTOR 3 DEFICIENCY", "Platelet Factor 3 Deficiency", "platelet factor 3 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "platelet factor 3 deficiency", "shortest_name_length": 28}
{"curie": "UMLS:C5204116", "names": ["AHL Amyloidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AHL Amyloidosis", "shortest_name_length": 15}
{"curie": "UMLS:C4682567", "names": ["Stage I Uterine Corpus Endometrial Stromal Sarcoma", "Stage I Uterine Corpus Endometrial Stromal Sarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Uterine Corpus Endometrial Stromal Sarcoma AJCC v8", "shortest_name_length": 50}
{"curie": "MONDO:0007441", "names": ["DI-2", "DGI1", "DGI-2", "DGI-II", "CAPDEPONT TEETH", "Capdepont teeth", "OPALESCENT DENTIN", "opalescent dentin", "DENTINOGENESIS IMPERFECTA 1", "dentinogenesis imperfecta 1", "Hereditary opalescent dentine", "Dentinogenesis imperfecta type 2", "dentinogenesis imperfecta type 1", "dentinogenesis imperfecta type 2", "Dentinogenesis Imperfecta, Shields Type 2", "dentinogenesis imperfecta, Shields type 2", "Dentinogenesis imperfecta, Shields type 2", "Dentinogenesis Imperfecta, Shields Type II", "dentinogenesis imperfecta, Shields type II", "DENTINOGENESIS IMPERFECTA, SHIELDS TYPE II", "Dentinogenesis imperfecta - Shield's type II", "OPALESCENT TEETH WITHOUT OSTEOGENESIS IMPERFECTA", "Opalescent Teeth without Osteogenesis Imperfecta", "opalescent teeth without osteogenesis imperfecta", "Dentinogenesis imperfecta - Shield's type II (disorder)", "DENTINOGENESIS IMPERFECTA WITHOUT OSTEOGENESIS IMPERFECTA", "Dentinogenesis imperfecta without osteogenesis imperfecta", "Dentinogenesis Imperfecta without Osteogenesis Imperfecta", "dentinogenesis imperfecta without osteogenesis imperfecta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dentinogenesis imperfecta type 2", "shortest_name_length": 4}
{"curie": "MONDO:0012303", "names": ["Mgr8", "MGR8", "migraine, susceptibility to, 8", "migraine with or without aura, susceptibility to, 8", "MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 8", "migraine with or without aura, susceptibility to, type 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "migraine with or without aura, susceptibility to, 8", "shortest_name_length": 4}
{"curie": "MONDO:0010187", "names": ["MCFD3", "Vkcfd", "VKCFD", "VKCFD1", "FMFD 3", "FMFD III", "vitamin K-dependent coagulation defect", "VITAMIN K-DEPENDENT COAGULATION DEFECT", "Vitamin K-Dependent Coagulation Defect", "multiple coagulation Factor deficiency 3", "Multiple Coagulation Factor Deficiency III", "MULTIPLE COAGULATION FACTOR DEFICIENCY III", "glutamic acid, deficient gamma-carboxylation of", "GLUTAMIC ACID, DEFICIENT GAMMA-CARBOXYLATION OF", "Glutamic Acid, Deficient Gamma-Carboxylation Of", "familial multiple coagulation Factor deficiency 3", "factors II, VII, IX, and X, combined deficiency of", "Factors II, VII, IX, And X, Combined Deficiency Of", "FACTORS II, VII, IX, AND X, COMBINED DEFICIENCY OF", "FAMILIAL MULTIPLE COAGULATION FACTOR DEFICIENCY III", "Familial Multiple Coagulation Factor Deficiency III", "Hereditary combined deficiency of factors II, VII, IX and X", "hereditary combined deficiency of factors II, VII, IX and X", "combined deficiency of vitamin K-dependent clotting factors 1", "VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1", "vitamin K-dependent clotting factors, combined deficiency of, 1", "Vitamin K-Dependent Clotting Factors, Combined Deficiency Of, 1", "vitamin K-dependent clotting factors, combined deficiency of, type 1", "hereditary combined deficiency of vitamin K-dependent clotting factors", "Hereditary combined deficiency of vitamin K-dependent clotting factors", "GGCX congenital vitamin K-dependent coagulation factors combined deficiency", "Hereditary combined deficiency of vitamin K-dependent clotting factors (disorder)", "congenital vitamin K-dependent coagulation factors combined deficiency caused by mutation in GGCX"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitamin K-dependent clotting factors, combined deficiency of, type 1", "shortest_name_length": 5}
{"curie": "MONDO:0004505", "names": ["Breast Central Papilloma", "Central Breast Papilloma", "central breast papilloma", "large duct breast papilloma", "Large Duct Breast Papilloma", "solitary intraductal breast papilloma", "Solitary Intraductal Breast Papilloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central breast papilloma", "shortest_name_length": 24}
{"curie": "MONDO:0004980", "names": ["ECZEMA", "Eczema", "eczema", "Eczemas", "eczemas", "allergic", "Eczema NOS", "eczema nos", "Eczema, NOS", "atopic eczema", "eczematous rash", "Eczematous rash", "Localised eczema", "Localized eczema", "Atopic dermatitis", "atopic dermatitis", "Atopic Dermatitis", "Eczema (disorder)", "Besnier's prurigo", "eczema (diagnosis)", "allergic dermatitis", "eczematous dermatitis", "DERMATITIS ECZEMATOID", "ECZEMATOUS DERMATITIS", "eczematoid dermatitis", "Eczematous Dermatitis", "Eczematoid dermatitis", "Dermatitis eczematoid", "Eczematous dermatitis", "Dermatitis, Eczematous", "Atopic neurodermatitis", "dermatitis; eczematous", "Dermatitis, eczematous", "eczematous; dermatitis", "ECZEMATOUS SKIN LESIONS", "Eczematous Dermatitides", "Dermatitides, Eczematous", "Eczematous dermatitis, NOS", "allergic form of dermatitis", "eczematoid dermatitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atopic eczema", "shortest_name_length": 6}
{"curie": "UMLS:C1708257", "names": ["Great Vessel Perforation", "Perforation of great vessels"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perforation of great vessels", "shortest_name_length": 24}
{"curie": "UMLS:C4552186", "names": ["Gastrointestinal vascular malformation hemorrhagic", "Gastrointestinal vascular malformation haemorrhagic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal vascular malformation hemorrhagic", "shortest_name_length": 50}
{"curie": "MONDO:0013180", "names": ["ASRT8", "Rhinoconjunctivitis, susceptibility to", "RHINOCONJUNCTIVITIS, SUSCEPTIBILITY TO", "asthma-RELATED traits, susceptibility to, 8", "ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 8", "asthma-related traits, susceptibility to, 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "asthma-related traits, susceptibility to, 8", "shortest_name_length": 5}
{"curie": "UMLS:C0948011", "names": ["Uterine cervix bleeding", "Cervix hemorrhage uterine", "Cervix haemorrhage uterine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervix hemorrhage uterine", "shortest_name_length": 23}
{"curie": "UMLS:C1332442", "names": ["BRCA1 Syndrome", "Early Onset Breast Ovarian Cancer Syndrome", "BRCA1-Associated Hereditary Breast and Ovarian Cancer Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "BRCA1-Associated Hereditary Breast and Ovarian Cancer Syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0019377", "names": ["Mycoplasma encephalitis", "Mycoplasma pneumoniae infectious encephalitis", "Mycoplasma pneumoniae caused infectious encephalitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mycoplasma encephalitis", "shortest_name_length": 23}
{"curie": "UMLS:C1112440", "names": ["Cardiac valve vegetation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiac valve vegetation", "shortest_name_length": 24}
{"curie": "UMLS:C1336050", "names": ["Spinal Degenerative Disease", "Spinal Degenerative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spinal Degenerative Disorder", "shortest_name_length": 27}
{"curie": "MONDO:0009592", "names": ["Bellini syndrome", "wedge-shaped epiphyses of knees", "Wedge-shaped epiphyses of knees", "wedge-Shaped epiphyses of knees", "METAPHYSEAL ACROSCYPHODYSPLASIA", "metaphyseal acroscyphodysplasia", "WEDGE-SHAPED EPIPHYSES OF KNEES", "Metaphyseal acroscyphodysplasia", "Bellini Chiumello Rimoldi syndrome", "cupped metaphyses and cone-Shaped epiphyses of knees with brachydactyly", "CUPPED METAPHYSES AND CONE-SHAPED EPIPHYSES OF KNEES WITH BRACHYDACTYLY", "wedge-shaped epiphyses of the knees with mental retardation and short stature", "intellectual disability-short stature-wedge-shaped epiphyses of knees syndrome", "Intellectual disability-short stature-wedge-shaped epiphyses of knees syndrome", "wedge-shaped epiphyses of the knees with intellectual disability and short stature"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metaphyseal acroscyphodysplasia", "shortest_name_length": 16}
{"curie": "UMLS:C0851980", "names": ["Peritoneal infection", "Peritoneal Infection", "peritoneal infection", "infection; peritoneal", "peritoneal infections", "peritoneal; infection", "Peritoneal infections", "peritoneal infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peritoneal Infection", "shortest_name_length": 20}
{"curie": "UMLS:C3273123", "names": ["Gallbladder Goblet Cell Carcinoid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gallbladder Goblet Cell Carcinoid", "shortest_name_length": 33}
{"curie": "MONDO:0003717", "names": ["Renal Pelvis Papillary Tumor", "renal pelvis papillary tumor", "Papillary Tumor of Renal Pelvis", "Papillary tumor of renal pelvis", "papillary tumor of renal pelvis", "Papillary tumour of renal pelvis", "Papillary Neoplasm of Renal Pelvis", "Papillary neoplasm of renal Pelvis", "papillary neoplasm of renal pelvis", "papillary tumor of the renal pelvis", "Papillary Tumor of the Renal Pelvis", "papillary neoplasm of the renal pelvis", "Papillary Neoplasm of the Renal Pelvis", "Renal Pelvis Papillary Urothelial Neoplasm", "renal pelvis papillary urothelial neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal pelvis papillary tumor", "shortest_name_length": 28}
{"curie": "MONDO:0021540", "names": ["lung hamartoma", "hamartoma lung", "Lung Hamartoma", "LUNG, HAMARTOMA", "Hamartoma of lung", "Hamartoma of Lung", "hamartoma of lung", "Pulmonary hamartoma", "pulmonary hamartoma", "Pulmonary Hamartoma", "hamartoma of the lung", "Hamartoma of the Lung", "lung chondroid hamartoma", "Lung Chondroid Hamartoma", "lung hamartoma (disease)", "Hamartoma of lung (disorder)", "hamartoma of lung (diagnosis)", "Pulmonary hamartoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hamartoma of lung", "shortest_name_length": 14}
{"curie": "MONDO:8000001", "names": ["staphylococcus discitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "staphylococcus discitis", "shortest_name_length": 23}
{"curie": "UMLS:C4727106", "names": ["Breast Carcinoma Metastatic in Lymph Node", "Metastatic Breast Cancer in the Lymph Nodes", "Breast Carcinoma Metastatic in the Lymph Nodes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Carcinoma Metastatic in the Lymph Nodes", "shortest_name_length": 41}
{"curie": "MONDO:0017196", "names": ["Al Gazali-Nair syndrome", "Al Gazali Nair syndrome", "Al Gazali Sabrinathan Nair syndrome", "osteogenesis imperfecta retinopathy seizures intellectual deficit", "osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome", "Osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome", "Osteogenesis imperfecta, retinopathy, seizures, intellectual disability syndrome", "Osteogenesis imperfecta, retinopathy, seizures, intellectual disability syndrome (disorder)", "Osteogenesis imperfecta, retinopathy, seizures, intellectual disability syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0004449", "names": ["Intraductal Breast Myoepitheliosis", "intraductal breast myoepitheliosis", "Breast Intraductal Myoepitheliosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intraductal breast myoepitheliosis", "shortest_name_length": 34}
{"curie": "UMLS:C1321482", "names": ["Behçet disease affecting oral mucosa", "Behçet's disease affecting oral mucosa", "Oral ulceration due to Behçet's disease", "Behçet's disease affecting oral mucosa (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Behçet's disease affecting oral mucosa", "shortest_name_length": 36}
{"curie": "MONDO:0002004", "names": ["atheroembolism of kidney", "kidney cholesterol embolism", "cholesterol embolism of kidney"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atheroembolism of kidney", "shortest_name_length": 24}
{"curie": "UMLS:C0919883", "names": ["Puncture site bleeding", "Puncture site hemorrhage", "Puncture site haemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Puncture site hemorrhage", "shortest_name_length": 22}
{"curie": "MONDO:0014522", "names": ["RDOB", "retinal dystrophy and obesity", "RETINAL DYSTROPHY AND OBESITY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal dystrophy and obesity", "shortest_name_length": 4}
{"curie": "UMLS:C1332049", "names": ["AIDS-Related Malignant Anal Tumor", "AIDS-Related Malignant Anal Neoplasm", "AIDS-Related Malignant Tumor of Anus", "AIDS-Related Malignant Neoplasm of Anus", "AIDS-Related Malignant Tumor of the Anus", "AIDS-Related Malignant Neoplasm of the Anus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Malignant Anal Neoplasm", "shortest_name_length": 33}
{"curie": "UMLS:C0016509", "names": ["Foot Dermatosis", "Foot Dermatoses", "Dermatosis, Foot", "Dermatoses, Foot"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Foot Dermatoses", "shortest_name_length": 15}
{"curie": "MONDO:0011089", "names": ["PDV", "PSVS", "patent ductus venosus", "Patent Ductus Venosus", "Patent ductus venosus", "PATENT DUCTUS VENOSUS", "Patent ductus venosus (disorder)", "Congenital portosystemic venous shunt", "Portosystemic Venous Shunt, Congenital", "portosystemic Venous shunt, congenital", "PORTOSYSTEMIC VENOUS SHUNT, CONGENITAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "patent ductus venosus", "shortest_name_length": 3}
{"curie": "UMLS:C4521968", "names": ["Stage III Lung Cancer", "Stage III Lung Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Lung Cancer AJCC v7", "shortest_name_length": 21}
{"curie": "MONDO:0032591", "names": ["HRPTTN", "Transient neonatal hyperparathyroidism", "Transient Neonatal Hyperparathyroidism", "hyperparathyroidism, transient neonatal", "HYPERPARATHYROIDISM, TRANSIENT NEONATAL", "Transient neonatal hyperparathyroidism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperparathyroidism, transient neonatal", "shortest_name_length": 6}
{"curie": "UMLS:C1708666", "names": ["Leaflet Disruption"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leaflet Disruption", "shortest_name_length": 18}
{"curie": "UMLS:C0278751", "names": ["localized mesothelial sarcoma", "mesothelial sarcoma, localized", "Mesothelioma malignant localized", "Localized Malignant Mesothelioma", "localized malignant mesothelioma", "Mesothelioma malignant localised", "malignant mesothelioma, localized", "mesothelioma, malignant, localized"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mesothelioma malignant localised", "shortest_name_length": 29}
{"curie": "UMLS:C3641710", "names": ["ENSAT Stage II Adrenal Cortex Cancer", "ENSAT Stage II Adrenal Cortex Carcinoma", "ENSAT Stage II Adrenal Cortical Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ENSAT Stage II Adrenal Cortical Carcinoma", "shortest_name_length": 36}
{"curie": "MONDO:0015067", "names": ["colonic NET", "NET of the colon", "carcinoid tumor of colon", "Colon Neuroendocrine Tumor", "colon neuroendocrine tumor", "neuroendocrine neoplasm of the colon", "neuroendocrine tumor of the colon, well differentiated, low or intermediate grade tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuroendocrine tumor of the colon, well differentiated, low or intermediate grade tumor", "shortest_name_length": 11}
{"curie": "MONDO:0024296", "names": ["Vascular Tumor", "vascular tumor", "Vascular Tumors", "vascular tumors", "tumors, vascular", "Tumors, Vascular", "Vascular Neoplasm", "vascular neoplasm", "Vascular Neoplasms", "vascular neoplasms", "Neoplasms, Vascular", "neoplasms, vascular", "Vascular tumor, NOS", "vascular system tumor", "vascular tissue tumor", "Vascular Tissue Tumor", "vascular system neoplasm", "tumor of vascular tissue", "vascular tissue neoplasm", "Vascular Tissue Neoplasm", "Tumor of Vascular Tissue", "tumor of vascular system", "Neoplasm of Vascular Tissue", "neoplasm of vascular tissue", "neoplasm of vascular system", "vascular system neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vascular neoplasm", "shortest_name_length": 14}
{"curie": "MONDO:0004956", "names": ["metastatic prostate cancer", "cancer metastatic prostate", "Prostate Cancer Metastatic", "Prostate cancer metastatic", "Metastatic Prostate Cancer", "PROSTATE CANCER METASTATIC", "Metastatic prostate cancer", "prostate cancer metastatic", "cancer metastatic prostatic", "metastatic prostatic cancer", "Prostatic cancer metastatic", "prostate carcinoma metastatic", "Prostate Carcinoma Metastatic", "Metastatic Prostate Carcinoma", "metastatic prostate carcinoma", "Carcinoma of the prostate metastatic", "Cancer of the prostate with metastasis", "Metastasis from malignant tumor of prostate", "Metastasis from malignant tumour of prostate", "metastasis from malignant neoplasm of prostate", "Metastasis from malignant tumor of prostate (disorder)", "metastasis from malignant neoplasm of prostate (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metastatic prostate carcinoma", "shortest_name_length": 26}
{"curie": "UMLS:C0023429", "names": ["Leukemia P388", "P388, Leukemia", "P388D(1) Leukemia", "mouse leukemia P388"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leukemia P388", "shortest_name_length": 13}
{"curie": "MONDO:0004494", "names": ["hepatoid pattern testicular yolk sac tumor", "testicular yolk sac tumor, hepatoid pattern", "Testicular Yolk Sac Tumor, Hepatoid Pattern"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular yolk sac tumor, hepatoid pattern", "shortest_name_length": 42}
{"curie": "MONDO:0012359", "names": ["CID due to partial RAG1 deficiency", "CID with expansion of gamma delta T cells", "combined immunodeficiency due to partial RAG1 deficiency", "Combined immunodeficiency due to partial RAG1 deficiency", "Combined immunodeficiency with expansion of gamma delta T cell", "Combined immunodeficiency with expansion of gamma delta T cells", "combined immunodeficiency with expansion of gamma delta T cells", "Combined immunodeficiency due to partial recombination-activating gene 1 deficiency", "Combined immunodeficiency due to partial recombination-activating gene 1 deficiency (disorder)", "Combined immunodeficiency due to partial recombination-activating gene 1 deficiency (diagnosis)", "Alpha-Beta T-Cell Lymphopenia with Gamma-Delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity", "alpha/beta T-cell lymphopenia with gamma/DELTA T-cell expansion, severe CYTOMEGALOVIRUS infection, and autoimmunity", "ALPHA/BETA T-CELL LYMPHOPENIA WITH GAMMA/DELTA T-CELL EXPANSION, SEVERE CYTOMEGALOVIRUS INFECTION, AND AUTOIMMUNITY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined immunodeficiency due to partial RAG1 deficiency", "shortest_name_length": 34}
{"curie": "MONDO:0001838", "names": ["Gonococcal prostatitis", "gonococcal prostatitis", "Acute gonococcal prostatitis", "acute gonococcal prostatitis", "gonococcal prostatitis, acute", "Gonococcal prostatitis (acute)", "gonococcal prostatitis (acute)", "Acute gonococcal prostatitis (disorder)", "acute gonococcal prostatitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute gonococcal prostatitis", "shortest_name_length": 22}
{"curie": "MONDO:0009946", "names": ["P5N DEFICIENCY", "P5N deficiency", "UMPH1 DEFICIENCY", "Umph1 deficiency", "UMPH1 Deficiency", "UMPH1 deficiency", "Hemolytic Anemia due to P5N Deficiency", "hemolytic Anemia due to P5N deficiency", "HEMOLYTIC ANEMIA DUE TO P5N DEFICIENCY", "hemolytic Anemia due to Umph1 deficiency", "HEMOLYTIC ANEMIA DUE TO UMPH1 DEFICIENCY", "Hemolytic Anemia due to UMPH1 Deficiency", "anemia, hemolytic, due to UMPH1 deficiency", "Uridine 5'-monophosphate hydrolase deficiency", "uridine 5'-monophosphate hydrolase deficiency", "hemolytic anemia due to pyrimidine 5' nucleotidase deficiency", "Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency", "pyrimidine 5-prime Nucleotidase deficiency, hemolytic Anemia due to", "PYRIMIDINE 5-PRIME NUCLEOTIDASE DEFICIENCY, HEMOLYTIC ANEMIA DUE TO", "Pyrimidine 5-Prime Nucleotidase Deficiency, Hemolytic Anemia due to", "Hemolytic Anemia due to Uridine 5-Prime Monophosphate Hydrolase Deficiency", "URIDINE 5-PRIME MONOPHOSPHATE HYDROLASE DEFICIENCY, HEMOLYTIC ANEMIA DUE TO", "uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to", "Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemolytic anemia due to pyrimidine 5' nucleotidase deficiency", "shortest_name_length": 14}
{"curie": "MONDO:0033618", "names": ["VIBOS", "Vissers-Bodmer syndrome", "VISSERS-BODMER SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vissers-Bodmer syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C4683557", "names": ["Non-Hodgkin Lymphoma by Ann Arbor Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Hodgkin Lymphoma by Ann Arbor Stage", "shortest_name_length": 39}
{"curie": "UMLS:C0341010", "names": ["Angina bullosa hemorrhagica", "Angina bullosa haemorrhagica", "Traumatic oral hemorrhagic bulla", "Traumatic oral haemorrhagic bulla", "Traumatic oral hemorrhagic bulla (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Traumatic oral hemorrhagic bulla", "shortest_name_length": 27}
{"curie": "MONDO:0008983", "names": ["CHROMOSOMAL INSTABILITY WITH TISSUE-SPECIFIC RADIOSENSITIVITY", "chromosomal instability with tissue-specific radiosensitivity", "Chromosomal Instability with Tissue-Specific Radiosensitivity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosomal instability with tissue-specific radiosensitivity", "shortest_name_length": 61}
{"curie": "UMLS:C0849835", "names": ["lip bleed", "Lip bleeding", "bleeding lip", "lip bleeding", "bleeding lips", "Bleeding lips", "Bleeding;lips", "lips bleeding", "Lip hemorrhage", "Lip haemorrhage", "Hemorrhage lips", "Haemorrhage lips", "bleeding from the lips", "lip bleeding (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lip hemorrhage", "shortest_name_length": 9}
{"curie": "UMLS:C1512860", "names": ["Sertoli-Leydig cell tumor of intermediate differentiation", "Moderately Differentiated Ovarian Sertoli-Leydig Cell Tumor", "Intermediate Differentiated Ovarian Sertoli-Leydig Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Moderately Differentiated Ovarian Sertoli-Leydig Cell Tumor", "shortest_name_length": 57}
{"curie": "UMLS:C0235820", "names": ["Dummy foal syndrome", "neonatal encephalopathy", "ENCEPHALOPATHY NEONATAL", "encephalopathy neonatal", "Encephalopathy neonatal", "Neonatal encephalopathy", "Neonatal Encephalopathy", "Neonatal encephalopathy (disorder)", "Neonatal encephalopathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neonatal encephalopathy", "shortest_name_length": 19}
{"curie": "UMLS:C1333144", "names": ["Congenital Disorder of Natural Immunity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Disorder of Natural Immunity", "shortest_name_length": 39}
{"curie": "UMLS:C5419973", "names": ["Digestive System Lipoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Digestive System Lipoma", "shortest_name_length": 23}
{"curie": "MONDO:0001583", "names": ["diabetic polyneuropathy", "diabetes polyneuropathy", "polyneuropathy diabetes", "Diabetic polyneuropathy", "Diabetic Polyneuropathy", "Polyneuropathy, Diabetic", "diabetics polyneuropathy", "Diabetic Polyneuropathies", "polyneuropathy in diabetes", "Polyneuropathy in diabetes", "Polyneuropathies, Diabetic", "Diabetic polyneuropathy, NOS", "NEUROPATHY DIABETIC POLYNEUROPATHY", "diabetic polyneuropathy (diagnosis)", "Diabetes mellitus with polyneuropathy", "diabetes mellitus with polyneuropathy", "diabetes with diabetic polyneuropathy", "Polyneuropathy due to diabetes mellitus", "polyneuropathy; diabetes (manifestation)", "diabetes; polyneuropathy (manifestation)", "diabetes with diabetic polyneuropathy (diagnosis)", "Polyneuropathy due to diabetes mellitus (disorder)", "diabetes; neuropathy, polyneuropathy (manifestation)", "neuropathy; diabetes, polyneuropathy (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diabetic polyneuropathy", "shortest_name_length": 23}
{"curie": "MONDO:0700030", "names": ["complete trisomy 21", "standard trisomy 21"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complete trisomy 21", "shortest_name_length": 19}
{"curie": "MONDO:0032664", "names": ["CILD40", "primary ciliary dyskinesia 40", "ciliary dyskinesia, primary, 40", "CILIARY DYSKINESIA, PRIMARY, 40", "primary ciliary dyskinesia 40 with or without situs inversus", "CILIARY DYSKINESIA, PRIMARY, 40, WITH OR WITHOUT SITUS INVERSUS", "Ciliary Dyskinesia, Primary, 40, With or Without Situs Inversus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ciliary dyskinesia, primary, 40", "shortest_name_length": 6}
{"curie": "UMLS:C1370868", "names": ["Refractory CML", "Refractory CGL", "Refractory Chronic Myeloid Leukemia", "Refractory Chronic Myelocytic Leukemia", "Refractory Chronic Myelogenous Leukemia", "Refractory Chronic Granulocytic Leukemia", "Refractory Chronic Myelogenous Leukemia (CML)", "recurrent chronic myelogenous leukemia, BCR-ABL1-positive", "Refractory Chronic Myelogenous Leukemia, BCR-ABL1 Positive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Chronic Myelogenous Leukemia, BCR-ABL1 Positive", "shortest_name_length": 14}
{"curie": "MONDO:0020450", "names": ["azygos continuation of the IVC", "azygos continuation of the inferior vena cava", "azygos continuation of the inferior caval vein"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "azygos continuation of the inferior vena cava", "shortest_name_length": 30}
{"curie": "MONDO:0004517", "names": ["ureter tuberculosis", "Tuberculosis ureter", "tuberculosis of ureter", "Tuberculosis of ureter", "TB - Tuberculosis of ureter", "Tuberculosis of ureter (disorder)", "tuberculosis of ureter (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ureter tuberculosis", "shortest_name_length": 19}
{"curie": "UMLS:C4725793", "names": ["Metastatic Bladder Urothelial Cancer", "Metastatic Bladder Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Bladder Urothelial Carcinoma", "shortest_name_length": 36}
{"curie": "MONDO:0060690", "names": ["phenytoin toxicity", "PHENYTOIN TOXICITY", "fetal hydantoin syndrome", "ARENE OXIDE DETOXIFICATION DEFECT", "arene oxide detoxification defect", "Arene Oxide Detoxification Defect", "diphenylhydantoin, defect in hydroxylation of", "DIPHENYLHYDANTOIN, DEFECT IN HYDROXYLATION OF", "Diphenylhydantoin, Defect in Hydroxylation of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phenytoin toxicity", "shortest_name_length": 18}
{"curie": "MONDO:0018779", "names": ["hypercontractile muscle stiffness syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypercontractile muscle stiffness syndrome", "shortest_name_length": 42}
{"curie": "UMLS:C0002889", "names": ["Microangiopathic Anemia", "Anemia, Microangiopathic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anemia, Microangiopathic", "shortest_name_length": 23}
{"curie": "UMLS:C1335401", "names": ["Philadelphia Chromosome Negative BCR-ABL1 Negative Chronic Myelogenous Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Philadelphia Chromosome Negative BCR-ABL1 Negative Chronic Myelogenous Leukemia", "shortest_name_length": 79}
{"curie": "MONDO:0005736", "names": ["eee", "EEE", "eastern equine encephalitis", "Eastern Equine Encephalitis", "Encephalitis eastern equine", "Eastern equine encephalitis", "Encephalitis, Eastern equine", "eastern equine; encephalitis", "ENCEPHALITIS, EASTERN EQUINE", "Equine Encephalitis, Eastern", "Encephalitis, Eastern Equine", "encephalitis; eastern equine", "encephalitis; equine, eastern", "equine; encephalitis, eastern", "Eastern Equine Encephalitides", "Encephalitides, Eastern Equine", "Equine Encephalitides, Eastern", "Eastern Equine Encephalomyelitis", "Eastern equine encephalomyelitis", "EASTERN EQUINE ENCEPHALOMYELITIS", "EEE - Eastern equine encephalitis", "Encephalomyelitis, Eastern Equine", "Eastern Equine Encephalitis (EEE)", "Equine Encephalomyelitis, Eastern", "Equine encephalitis, Eastern (EEE)", "Eastern Equine Encephalomyelitides", "Equine Encephalomyelitides, Eastern", "Encephalomyelitides, Eastern Equine", "Eastern equine encephalitis (diagnosis)", "Eastern equine encephalitis virus infection", "Eastern Equine Encephalomyelitis Virus Infection", "Eastern equine encephalitis virus infection (disorder)", "Eastern equine encephalitis virus neuroinvasive disease", "Neuroinvasive Eastern equine encephalitis virus disease", "Neuroinvasive Eastern equine encephalitis virus infection", "Neuroinvasive Eastern equine encephalitis virus infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eastern equine encephalitis", "shortest_name_length": 3}
{"curie": "MONDO:0001630", "names": ["retinal artery branch occlusion", "branch retinal artery occlusion", "Branch Retinal Artery Occlusion", "Branch retinal artery occlusion", "Retinal artery branch occlusion", "arterial retinal branch occlusion", "Arterial retinal branch occlusion", "retinal arterial branch occlusion", "Retinal arterial branch occlusion", "Retinal Arterial Branch Occlusion", "occlusion of retinal arterial branch", "BRAO - Branch retinal artery occlusion", "Arterial retinal branch occlusion (disorder)", "occlusion; artery, retina (partial) (branch)", "artery; occlusion, retina (partial) (branch)", "occlusion of retinal arterial branch (diagnosis)", "retinal artery branch occlusion (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "branch retinal artery occlusion", "shortest_name_length": 31}
{"curie": "MONDO:0001105", "names": ["HYPERTENSION RENAL", "renal hypertension", "RENAL HYPERTENSION", "Hypertension renal", "hypertension renal", "Renal Hypertension", "Renal hypertension", "Renal Hypertensions", "Hypertension, renal", "Hypertension, Renal", "renal; hypertension", "Renal hypertensions", "hypertension; renal", "Hypertensions, Renal", "Renal hypertension NOS", "Hypertension;cardiorenal", "cardiorenal; hypertension", "renovascular hypertension", "Renal hypertension (disorder)", "hypertension secondary to renal disorders", "secondary hypertension to renal disorders", "hypertension secondary to renal disorders (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal hypertension", "shortest_name_length": 18}
{"curie": "MONDO:0016535", "names": ["HED", "EDA", "CST syndrome", "anhidrotic ectodermal dysplasia", "ectodermal dysplasia anhidrotic", "hypohidrotic ectodermal dysplasia", "anhidrotic ectodermal dysplasia 3", "anhidrotic ectodermal dysplasia 1", "Anhidrotic Ectodermal Dysplasia 1", "ectodermal dysplasia 1, Anhydrotic", "ectodermal dysplasia, hypohidrotic", "hypohidrotic X-linked ectodermal dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypohidrotic ectodermal dysplasia", "shortest_name_length": 3}
{"curie": "MONDO:0004153", "names": ["Embryonal Carcinoma of Childhood CNS", "embryonal carcinoma of pediatric CNS", "Embryonal carcinoma of pediatric CNS", "Embryonal Carcinoma of Pediatric CNS", "embryonal carcinoma of childhood CNS", "Embryonal carcinoma of paediatric CNS", "pediatric CNS embryonal cell carcinoma", "childhood CNS embryonal cell carcinoma", "Childhood CNS Embryonal Cell Carcinoma", "Pediatric CNS Embryonal Cell Carcinoma", "paediatric CNS embryonal cell carcinoma", "Embryonal Carcinoma of the Pediatric CNS", "Embryonal Carcinoma of the Childhood CNS", "embryonal carcinoma of the pediatric CNS", "embryonal carcinoma of the childhood CNS", "pediatric central nervous system embryonal carcinoma", "Pediatric Central Nervous System Embryonal Carcinoma", "Childhood Central Nervous System Embryonal Carcinoma", "childhood central nervous system embryonal carcinoma", "Embryonal Carcinoma of Pediatric Central Nervous System", "embryonal carcinoma of pediatric central nervous system", "embryonal carcinoma of childhood central nervous system", "Embryonal Carcinoma of Childhood Central Nervous System", "embryonal carcinoma of the childhood central nervous system", "Embryonal Carcinoma of the Pediatric Central Nervous System", "Embryonal Carcinoma of the Childhood Central Nervous System", "embryonal carcinoma of the pediatric central nervous system", "childhood embryonal carcinoma of the central nervous system", "pediatric embryonal carcinoma of the central nervous system", "embryonal carcinoma of the central nervous system of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood central nervous system embryonal carcinoma", "shortest_name_length": 36}
{"curie": "UMLS:C4086152", "names": ["Astrocytoma", "childhood astrocytoma", "Childhood Astrocytoma", "astrocytoma, childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Astrocytoma", "shortest_name_length": 11}
{"curie": "UMLS:C0038157", "names": ["staphylococcal enterocolitis", "STAPHYLOCOCCAL ENTEROCOLITIS", "Staphylococcal enterocolitis", "Staphylococcus aureus gastroenteritis", "Staphylococcus aureus Gastroenteritis", "Staphylococcal enterocolitis (disorder)", "staphylococcal enterocolitis (diagnosis)", "Intestinal infection due to staphylococcus", "gastroenteritis due to Staphylococcus aureus", "Staphylococcus aureus gastroenteritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Staphylococcal enterocolitis", "shortest_name_length": 28}
{"curie": "MONDO:0004819", "names": ["indolent myeloma", "Indolent myeloma", "indolent multiple myeloma", "Indolent Multiple Myeloma", "Indolent multiple myeloma", "Indolent Plasma Cell Myeloma", "indolent plasma cell myeloma", "Indolent multiple myeloma (disorder)", "indolent multiple myeloma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "indolent plasma cell myeloma", "shortest_name_length": 16}
{"curie": "MONDO:0013256", "names": ["WITKOS", "Del(15)(q24)", "Monosomy 15q24", "monosomy 15q24", "15q24 deletion", "15q24 Deletion", "15q24 microdeletion", "15q24 Microdeletion", "Witteveen-Kolk syndrome", "Witteveen Kolk syndrome", "WITTEVEEN-KOLK SYNDROME", "15q24 Microdeletion Syndrome", "15q24 microdeletion syndrome", "WITKOS - Witteveen Kolk syndrome", "Microdeletion of chromosome 15q24", "Witteveen Kolk syndrome (disorder)", "CHROMOSOME 15q24 DELETION SYNDROME", "chromosome 15q24 deletion syndrome", "CHROMOSOME 15q24 DUPLICATION SYNDROME", "chromosome 15Q24 Duplication syndrome", "15q24 recurrent microdeletion syndrome", "Interstitial deletion of chromosome 15q24", "Interstitial Deletion of Chromosome 15q24", "Microdeletion of chromosome 15q24 (disorder)", "SIN3A-related intellectual disability syndrome", "SIN3A (Switch-insensitive 3 transcription regulator family member A)-related intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 15q24 deletion syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0002707", "names": ["Mucinous Breast Cancer", "mucinous breast cancer", "Colloid Breast Carcinoma", "colloid breast carcinoma", "breast mucinous carcinoma", "mucinous breast carcinoma", "Mucinous Breast Carcinoma", "Mucinous breast carcinoma", "Breast Mucinous Carcinoma", "colloid carcinoma of breast", "Colloid Carcinoma of Breast", "mucinous carcinoma of breast", "Mucinous Carcinoma of Breast", "Mucinous carcinoma of breast", "Colloid Carcinoma of the Breast", "ductal colloid breast carcinoma", "colloid carcinoma of the breast", "colloid ductal breast carcinoma", "ductal mucinous breast carcinoma", "Mucinous Carcinoma of the Breast", "mucinous carcinoma of the breast", "Mucinous ductal breast carcinoma", "mucinous ductal breast carcinoma", "invasive colloid breast carcinoma", "Invasive Colloid Breast Carcinoma", "Invasive mucinous breast carcinoma", "invasive mucinous breast carcinoma", "Invasive Mucinous Breast Carcinoma", "Infiltrating Colloid Breast Carcinoma", "infiltrating colloid breast carcinoma", "Infiltrating Mucinous Breast Carcinoma", "infiltrating mucinous breast carcinoma", "Mucinous carcinoma of breast (disorder)", "Mucinous carcinoma of breast (diagnosis)", "breast invasive mixed mucinous carcinoma", "breast neoplasm malignant carcinoma mucinous"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast mucinous carcinoma", "shortest_name_length": 22}
{"curie": "MONDO:0018774", "names": ["EKC syndrome", "erythrokeratodermia-cardiomyopathy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythrokeratodermia-cardiomyopathy syndrome", "shortest_name_length": 12}
{"curie": "UMLS:C4277533", "names": ["Blood Vessel Dissection", "Dissection, Blood Vessel"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dissection, Blood Vessel", "shortest_name_length": 23}
{"curie": "MONDO:0024919", "names": ["Dog Disease", "dog disease", "disease dog", "Disease, Dog", "Dog Diseases", "disease, Dog", "diseases dog", "disease dogs", "dog diseases", "diseases, Dog", "diseases dogs", "Diseases, Dog", "disease canine", "canine disease", "Canine Disease", "Dogs--Diseases", "canine diseases", "disease, canine", "Canine Diseases", "Disease, Canine", "diseases, canine", "canines diseases", "Diseases, Canine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dog disease", "shortest_name_length": 11}
{"curie": "MONDO:0003010", "names": ["MCRCC", "Renal Cystadenocarcinoma", "renal cystadenocarcinoma", "Cystadenocarcinoma of kidney", "cystadenocarcinoma of kidney", "Multilocular clear cell carcinoma", "multilocular clear cell carcinoma", "Multilocular Cystic Renal Cell Cancer", "multilocular cystic renal cell cancer", "multilocular clear cell adenocarcinoma", "Multilocular clear cell adenocarcinoma", "Cystadenocarcinoma of kidney (disorder)", "Multilocular cystic renal cell carcinoma", "multilocular cystic renal cell carcinoma", "cystadenocarcinoma of kidney (diagnosis)", "multilocular clear cell renal cell carcinoma", "Multilocular Clear Cell Renal Cell Carcinoma", "Multilocular clear cell renal cell carcinoma", "Multilocular cystic renal cell adenocarcinoma", "multilocular cystic renal cell adenocarcinoma", "multilocular clear cell renal cell adenocarcinoma", "Multilocular clear cell renal cell adenocarcinoma", "multilocular cystic renal neoplasm of low malignant potential", "Multilocular cystic renal neoplasm of low malignant potential", "Multilocular Cystic Renal Neoplasm of Low Malignant Potential", "multilocular cystic clear cell renal cell neoplasm of low malignant potential"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multilocular clear cell renal cell carcinoma", "shortest_name_length": 5}
{"curie": "MONDO:0008121", "names": ["ONYCHOGRYPOSIS, PEDAL, WITH KERATOSIS PLANTARIS AND COARSE HAIR", "onychogryposis, pedal, with keratosis plantaris and coarse hair", "Onychogryposis, Pedal, with Keratosis Plantaris and Coarse Hair"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "onychogryposis, pedal, with keratosis plantaris and coarse hair", "shortest_name_length": 63}
{"curie": "UMLS:C5447502", "names": ["Advanced Intrahepatic Cholangiocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Intrahepatic Cholangiocarcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0012964", "names": ["monosomy 15q26", "Monosomy 15q26", "DRAYER SYNDROME", "Drayer syndrome", "Drayer Syndrome", "Distal monosomy 15q", "distal monosomy 15q", "15q26 deletion syndrome", "distal monosomy type 15q", "Distal 15q deletion syndrome", "Distal monosomy 15q syndrome", "distal 15q deletion syndrome", "Telomeric 15q deletion syndrome", "telomeric 15q deletion syndrome", "Chromosome 15q26-Qter Deletion Syndrome", "Distal monosomy 15q syndrome (disorder)", "chromosome 15q26-qter deletion syndrome", "CHROMOSOME 15q26-qter DELETION SYNDROME", "Distal monosomy 15q syndrome (diagnosis)", "chromosome 15q26-qter deletion syndrome, isolated cases", "deletion of part of chromosome 15 distal monosomy 15q syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 15q26-qter deletion syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C2826176", "names": ["AML with Gene Mutations", "Acute Myeloid Leukemia with Gene Mutations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Myeloid Leukemia with Gene Mutations", "shortest_name_length": 23}
{"curie": "UMLS:C1518225", "names": ["Malignant Non-Hodgkin Lymphoma, Cleaved Cell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Non-Hodgkin Lymphoma, Cleaved Cell", "shortest_name_length": 44}
{"curie": "MONDO:0011895", "names": ["HES", "hypereosinophilic syndrome idiopathic", "Idiopathic Hypereosinophilic Syndrome", "Idiopathic hypereosinophilic syndrome", "idiopathic hypereosinophilic syndrome", "Hypereosinophilic Syndrome, Idiopathic", "HYPEREOSINOPHILIC SYNDROME, IDIOPATHIC", "hypereosinophilic syndrome, idiopathic", "Idiopathic Hypereosinophilic Syndromes", "Syndrome, Idiopathic Hypereosinophilic", "Syndromes, Idiopathic Hypereosinophilic", "Hypereosinophilic Syndromes, Idiopathic", "Idiopathic hypereosinophilic syndrome (HES)", "Idiopathic hypereosinophilic syndrome (disorder)", "Idiopathic hypereosinophilic syndrome (diagnosis)", "Idiopathic hypereosinophilic syndrome (morphologic abnormality)", "hypereosinophilic syndrome, idiopathic, resistant to imatinib, isolated cases, somatic mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic hypereosinophilic syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0002397", "names": ["Liver Sarcoma", "liver sarcoma", "hepatic sarcoma", "Hepatic sarcoma", "Hepatic Sarcoma", "Sarcoma of Liver", "Sarcoma of liver", "sarcoma of liver", "sarcoma of the liver", "Sarcoma of the Liver", "Sarcoma of liver (disorder)", "sarcoma of liver (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "liver sarcoma", "shortest_name_length": 13}
{"curie": "UMLS:C0036986", "names": ["shock traumatic", "Traumatic shock", "Traumatic Shock", "traumatic shock", "shock; traumatic", "Shock, Traumatic", "traumatic; shock", "Traumatic shock, NOS", "Shock following injury", "traumatic shock disorder", "Traumatic shock (disorder)", "Shock following injury, NOS", "traumatic shock (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Shock, Traumatic", "shortest_name_length": 15}
{"curie": "MONDO:0009923", "names": ["ppsh", "PPSH", "Micropenis", "MICROPENIS", "micropenis", "Small penis", "Short penis", "micropenis (diagnosis)", "5a-reductase deficiency", "5-alpha-reductase deficiency", "5 alpha-reductase deficiency", "5 alpha deficiency reductase", "5-alpha reductase deficiency", "5-Alpha-Reductase Deficiency", "5-alpha-reductase; deficiency", "deficiency; 5-alpha-reductase", "micropenis (physical finding)", "Steroid 5a-reductase deficiency", "Steroid 5-alpha-reductase deficiency", "steroid 5-alpha-reductase deficiency", "5 Alpha steroid reductase 2 deficiency", "5 Alpha Steroid Reductase 2 Deficiency", "Steroid 5-alpha-reductase 2 deficiency", "pseudovaginal perineoscrotal hypospadias", "PSEUDOVAGINAL PERINEOSCROTAL HYPOSPADIAS", "Pseudovaginal Perineoscrotal Hypospadias", "Pseudovaginal perineoscrotal hypospadias", "5 alpha-reductase deficiency (diagnosis)", "46,XY DSD due to 5-alpha-reductase 2 deficiency", "PPSH - Pseudovaginal perineoscrotal hypospadias", "Familial incomplete male pseudohermaphroditism type 2", "3-Oxo-5 Alpha-Steroid Delta 4-Dehydrogenase Deficiency", "Familial Incomplete Male Pseudohermaphroditism, Type 2", "3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency", "FAMILIAL INCOMPLETE MALE PSEUDOHERMAPHRODITISM, TYPE 2", "3-oxo-5 Alpha-steroid Delta 4-dehydrogenase deficiency", "familial incomplete Male pseudohermaphroditism, type 2", "Familial incomplete male pseudohermaphroditism, type 2", "Male pseudohermaphroditism due to 5-alpha-reductase deficiency", "Male pseudohermaphroditism due to 5-Alpha-reductase deficiency", "Male Pseudohermaphroditism due to 5-Alpha-Reductase Deficiency", "MALE PSEUDOHERMAPHRODITISM DUE TO 5-ALPHA-REDUCTASE DEFICIENCY", "Male pseudohermaphroditism due to 5-alpha-reductase 2 deficiency", "3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency (disorder)", "46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency", "Male pseudohermaphroditism due to 5-alpha-reductase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0002041", "names": ["Mycosis", "Mycoses", "mycoses", "MYCOSES", "mycosis", "Mycosis, NOS", "Fungal Disease", "Fungus Disease", "fungal disease", "fungus disease", "Fungal Diseases", "fungus; disease", "Fungi infection", "Disease, Fungus", "Mycotic disease", "fungal diseases", "Disease, Fungal", "Fungus Diseases", "disease; fungus", "Infection;fungus", "Fungal (Mycotic)", "Diseases, Fungus", "FUNGAL INFECTION", "Infection fungal", "FUNGUS INFECTION", "Diseases, Fungal", "Fungal Infection", "INFECTION FUNGAL", "Fungal infection", "Fungus Infection", "Fungus infection", "fungal infection", "fungus infection", "Infection, Fungal", "infections, Fungi", "Mycoses (B35-B49)", "INFECTION MYCOTIC", "infection; fungus", "fungus; infection", "Infection mycotic", "Infection, Fungus", "fungal infections", "Fungal Infections", "fungus infections", "Fungus Infections", "mycotic; disorder", "mycotic infection", "Fungal infections", "infection, fungal", "infection; mycotic", "Mycosis (disorder)", "Infections, Fungus", "mycotic; infection", "Infections, Fungal", "Unspecified mycosis", "mycosis (diagnosis)", "Fungal infection NOS", "Fungus infection, NOS", "Fungal infection, NOS", "MYCOSES: GENERAL TERMS", "Fungi infectious disease", "diseases caused by fungi", "Diseases Caused by Fungi", "Disease caused by fungus", "Fungi disease or disorder", "fungal infectious disease", "Fungal infectious disease", "Fungal Infectious Disease", "Infection fungal (mycotic)", "Fungal infectious disorders", "fungal infection (diagnosis)", "Disease caused by fungus, NOS", "Fungal infectious disease, NOS", "disease (or disorder); mycotic", "Fungi caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fungal infectious disease", "shortest_name_length": 7}
{"curie": "OMIM:110500", "names": [], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"]}
{"curie": "UMLS:C3897736", "names": ["Recurrent Malignant Extragonadal Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Malignant Extragonadal Germ Cell Tumor", "shortest_name_length": 48}
{"curie": "UMLS:C0278506", "names": ["Stage III NSCLC", "stage III NSCLC", "NSCLC, stage III", "stage III nonsmall cell lung cancer", "non-oat cell lung cancer, stage III", "nonsmall cell lung cancer, stage III", "Lung cancer non-small cell stage III", "Non-small cell lung cancer stage III", "stage III non-small cell lung cancer", "Stage III Non-Small Cell Lung Cancer", "lung cancer, non-oat cell, stage III", "non-small cell lung cancer, stage III", "Stage III Non-Oat Cell Lung Carcinoma", "lung cancer, nonsmall cell, stage III", "lung cancer, non-small cell, stage III", "Stage III Non-Small Cell Lung Carcinoma", "Stage III Non-Oat Cell Carcinoma of Lung", "Stage III Non-Small Cell Carcinoma of Lung", "Stage III Non-Oat Cell Carcinoma of the Lung", "Stage III Non-Small Cell Lung Cancer AJCC v7", "Stage III Lung Non-Small Cell Cancer AJCC v7", "Stage III Non-Small Cell Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-small cell lung cancer stage III", "shortest_name_length": 15}
{"curie": "UMLS:C0856011", "names": ["Extranodal Marginal Zone B-Cell Lymphoma (MALT Type) Refractory", "Extranodal marginal zone B-cell lymphoma (MALT type) refractory", "Refractory Extranodal Marginal Zone B-Cell Lymphoma (MALT Type)", "Refractory Extranodal Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue", "Refractory Extranodal Marginal Zone B-Cell Lymphoma of Mucosa-Associated Lymphoid Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extranodal marginal zone B-cell lymphoma (MALT type) refractory", "shortest_name_length": 63}
{"curie": "UMLS:C5205873", "names": ["CUTANEOUS RADIATION INJURY", "Cutaneous Radiation Injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous Radiation Injury", "shortest_name_length": 26}
{"curie": "MONDO:0016913", "names": ["deletion 15q", "15q monosomy", "monosomy 15q", "15q deletion", "partial monosomy 15q", "chromosome 15q deletion", "Chromosome 15q, partial deletion", "partial deletion of chromosome 15q", "Partial monosomy of chromosome 15q", "partial monosomy of chromosome 15q", "Partial deletion of chromosome 15q", "Partial deletion of long arm of chromosome 15", "partial monosomy of the long arm of chromosome 15", "partial deletion of the long arm of chromosome 15", "Partial monosomy of the long arm of chromosome 15", "Partial deletion of the long arm of chromosome 15", "partial deletion of the long arm of chromosome type 15", "Partial deletion of long arm of chromosome 15 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of the long arm of chromosome 15", "shortest_name_length": 12}
{"curie": "MONDO:0021952", "names": ["APD", "Progesterone dermatitis", "progesterone dermatitis", "autoimmune progesterone urticaria", "Autoimmune progesterone urticaria", "Autoimmune progesterone dermatitis", "autoimmune progesterone dermatitis", "autoimmune progesterone dermatitis/urticaria", "Autoimmune progesterone dermatitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune progesterone dermatitis", "shortest_name_length": 3}
{"curie": "MONDO:0024913", "names": ["disease cattle", "bovine disease", "Cattle Disease", "cattle disease", "Bovine Disease", "Cattle Diseases", "Bovine Diseases", "cattle diseases", "disease, bovine", "diseases bovine", "Disease, Cattle", "bovine diseases", "disease, cattle", "Disease, Bovine", "Diseases, Bovine", "diseases, bovine", "Diseases, Cattle", "Cattle--Diseases", "diseases, cattle"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cattle disease", "shortest_name_length": 14}
{"curie": "MONDO:0006569", "names": ["Leg Dermatosis", "Leg Dermatoses", "leg dermatosis", "Dermatoses, Leg", "Dermatosis, Leg"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leg dermatosis", "shortest_name_length": 14}
{"curie": "MONDO:0015356", "names": ["familial tumor syndrome", "Familial Tumor Syndrome", "Hereditary Tumor Syndrome", "inherited cancer syndrome", "hereditary tumor syndrome", "Hereditary Cancer Syndrome", "hereditary cancer syndrome", "Cancer Syndrome, Hereditary", "hereditary cancer syndromes", "syndrome, hereditary cancer", "Syndrome, Hereditary Cancer", "Hereditary Cancer Syndromes", "cancer syndrome, hereditary", "Syndromes, Hereditary Cancer", "familial neoplastic syndrome", "syndromes, hereditary cancer", "cancer syndromes, hereditary", "Germline Neoplastic Syndrome", "Familial Neoplastic Syndrome", "Cancer Syndromes, Hereditary", "hereditary neoplastic syndrome", "Hereditary Neoplastic Syndrome", "Hereditary neoplastic syndrome", "Syndrome, Hereditary Neoplastic", "neoplastic syndrome, hereditary", "Neoplastic Syndrome, Hereditary", "syndrome, hereditary neoplastic", "hereditary neoplastic syndromes", "Hereditary Neoplastic Syndromes", "syndromes, hereditary neoplastic", "Syndromes, Hereditary Neoplastic", "Neoplastic Syndromes, Hereditary", "inherited cancer-predisposing syndrome", "Hereditary cancer-predisposing syndrome", "hereditary cancer-predisposing syndrome", "Hereditary cancer-predisposing syndrome (disorder)", "hereditary cancer-predisposing syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary neoplastic syndrome", "shortest_name_length": 23}
{"curie": "UMLS:C1334316", "names": ["Kadish Stage B Olfactory Neuroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kadish Stage B Olfactory Neuroblastoma", "shortest_name_length": 38}
{"curie": "UMLS:C0853336", "names": ["cornea; infiltrate", "Corneal Infiltrate", "corneal infiltrate", "infiltrate; cornea", "Corneal Infiltrates", "Corneal infiltrates", "corneal infiltrates", "Corneal Infiltration", "Infiltrate of cornea", "Infiltrate of cornea (disorder)", "corneal infiltrate (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infiltrate of cornea", "shortest_name_length": 18}
{"curie": "MONDO:0010643", "names": ["LEUKEMIA ACUTE", "leukemia acute", "Blast leukemia", "ACUTE LEUKEMIA", "Leukemia acute", "Acute leukemia", "Acute Leukemia", "acute leukemia", "Leukaemia acute", "acute leukemias", "acute leukaemia", "acute; leukemia", "LEUKAEMIA ACUTE", "Acute leukaemia", "Acute leukemias", "leukemia, acute", "leukemia; acute", "Blastic leukemia", "acute leukaemias", "blastic; leukemia", "leukemia; blastic", "Stem cell Leukemia", "LEUKEMIA STEM CELL", "Stem cell leukemia", "stem cell leukemia", "Acute blood cancer", "Leukemia stem cell", "Acute leukemia NOS", "LEUKEMIA, EMBRYONAL", "Acute leukaemia NOS", "Leukaemia stem cell", "Stem cell leukaemia", "LEUKEMIA, STEM CELL", "stem cell; leukemia", "stem cell leukaemia", "Blast cell leukemia", "Acute leukemia, NOS", "acute leukemia, NOS", "leukemia; stem cell", "Acute leukaemia, NOS", "LEUKEMIA, BLAST CELL", "Blast cell leukaemia", "Acute leukemia, disease", "stem cell acute leukemia", "acute leukemia (disease)", "Acute leukaemia, disease", "Leukemia undifferentiated", "leukemia, acute, X-linked", "LEUKEMIA, ACUTE, X-LINKED", "Undifferentiated leukemia", "Leukemia, Acute, X-Linked", "Leukaemia undifferentiated", "Undifferentiated leukaemia", "acute leukemia (diagnosis)", "undifferentiated; leukemia", "leukemia; undifferentiated", "stem cell leukemia (disease)", "LEUKEMIA, UNDIFFERENTIATED CELL", "Acute leukemia, disease (disorder)", "acute leukemia not otherwise specified", "Acute leukemia of unspecified cell type", "Acute leukemia (morphologic abnormality)", "Acute leukaemia of unspecified cell type", "Leukemia of unspecified cell type, acute", "Leukaemia of unspecified cell type, acute", "Acute leukemia, morphology, including blast cell OR undifferentiated leukemia", "Acute leukaemia, morphology, including blast cell OR undifferentiated leukaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute leukemia", "shortest_name_length": 14}
{"curie": "MONDO:0007625", "names": ["Oral mucosa epithelial hyperplasia", "Focal epithelial hyperplasia of oral mucosa", "FOCAL EPITHELIAL HYPERPLASIA OF THE ORAL MUCOSA", "Focal Epithelial Hyperplasia of the Oral Mucosa", "focal epithelial hyperplasia of the oral mucosa", "Focal epithelial hyperplasia of the lining of mouth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal epithelial hyperplasia of the oral mucosa", "shortest_name_length": 34}
{"curie": "MONDO:0020133", "names": ["posterior fossa malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "posterior fossa malformation", "shortest_name_length": 28}
{"curie": "MONDO:0016114", "names": ["childhood bulbospinal muscular atrophy", "pediatric bulbospinal muscular atrophy", "bulbospinal muscular atrophy of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bulbospinal muscular atrophy of childhood", "shortest_name_length": 38}
{"curie": "MONDO:0016217", "names": ["MdD", "MDD", "MdDS", "Mal de débarquement", "mal de Debarquement", "Mal de Debarquement", "Mal de debarquement", "disembarkment syndrome", "Disembarkment syndrome", "Sickness of disembarkment", "sickness of disembarkment", "Mal de debarquement syndrome", "Mal de Debarquement (diagnosis)", "Mal de debarquement syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mal de Debarquement", "shortest_name_length": 3}
{"curie": "MONDO:0015601", "names": ["VEODS", "MRXSVEOD", "VAN ESCH-O'DRISCOLL SYNDROME", "Van Esch-O'Driscoll syndrome", "X-linked intellectual disability Van Esch type", "X-linked intellectual disability, van Esch type", "X-linked intellectual disability, Van Esch type", "Van Esch-O'Driscoll syndrome, X-linked recessive", "X-linked intellectual disability Van Esch type (disorder)", "X-linked intellectual disability Van Esch type (diagnosis)", "X-linked syndromic mental retardation Van Esch-O'Driscoll type", "mental retardation, X-Linked, syndromic, Van Esch-O'Driscoll type", "MENTAL RETARDATION, X-LINKED, SYNDROMIC, VAN ESCH-O'DRISCOLL TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability, van Esch type", "shortest_name_length": 5}
{"curie": "MONDO:0004245", "names": ["ependymal glioma", "brain ependymoma", "ependymal tumors", "BRAIN, EPENDYMOMA", "GLIOMA, EPENDYMAL", "ependymoma of brain", "Ependymoma of brain", "Brain Ependymal Tumor", "ependymal brain tumor", "brain ependymal tumor", "ependymoma brain tumor", "BRAIN TUMOR, EPENDYMOMA", "Ependymal Tumor of Brain", "ependymal tumor of brain", "Ependymal tumor of brain", "Ependymal tumour of brain", "Ependymoma of brain (disorder)", "ependymoma of brain (diagnosis)", "INTRACRANIAL NEOPLASM, EPENDYMOMA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ependymal tumor of brain", "shortest_name_length": 16}
{"curie": "UMLS:C0272053", "names": ["Anemia due to enzyme deficiency", "Anaemia due to enzyme deficiency", "ANEMIAS DUE TO ENZYME DEFICIENCIES", "Anemia due to enzyme deficiency, NOS", "Anaemia due to enzyme deficiency, NOS", "Anemia due to enzyme deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anemia due to enzyme deficiency", "shortest_name_length": 31}
{"curie": "MONDO:0014277", "names": ["DDH2", "developmental dysplasia of the hip 2", "DEVELOPMENTAL DYSPLASIA OF THE HIP 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental dysplasia of the hip 2", "shortest_name_length": 4}
{"curie": "UMLS:C0235013", "names": ["hypervigilence", "Hyperalertness", "HYPERALERTNESS", "Hypervigilance", "hypervigilance", "hyper alertness", "Increased state of alertness", "hypervigilance (physical finding)", "behavior demonstrated hypervigilance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypervigilance", "shortest_name_length": 14}
{"curie": "MONDO:0006626", "names": ["NEUROPATHY DIABETIC", "Neuropathy;diabetic", "diabetic neuropathy", "DIABETIC NEUROPATHY", "Diabetic Neuropathy", "Diabetic neuropathy", "Neuropathy, Diabetic", "Neuropathy, diabetic", "NEUROPATHY, DIABETIC", "diabetic neuropathies", "Diabetic neuropathies", "Diabetic Neuropathies", "diabetic nerve damage", "Neuropathies, Diabetic", "Diabetes mellitus with neuropathy", "Neuropathy due to diabetes mellitus", "neuropathy; diabetes (manifestation)", "Diabetes with neurological manifestations", "Neuropathy due to diabetes mellitus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diabetic neuropathy", "shortest_name_length": 19}
{"curie": "MONDO:0005886", "names": ["THRUSH", "Thrush", "thrush", "Thrush NOS", "Oral muguet", "Thrush oral", "ORAL THRUSH", "Oral thrush", "oral thrush", "Thrush;oral", "Oral candida", "Thrush, oral", "thrush, oral", "oral moniliasis", "Oral Moniliases", "Moniliasis oral", "Oral candidosis", "ORAL MONILIASIS", "Oral Moniliasis", "Oral moniliasis", "MONILIASIS ORAL", "Moniliases, Oral", "Candidiasis;oral", "Oral Candidiasis", "Moniliasis, Oral", "oral candidiasis", "ORAL CANDIDIASIS", "Oral Candidiases", "Oral candidiasis", "Candida of mouth", "mouth candidiasis", "Candidiasis, oral", "CANDIDIASIS, ORAL", "thrush (disorder)", "Candidiases, Oral", "Candidiasis, Oral", "mycotic stomatitis", "STOMATITIS CANDIDA", "mouth; candidiasis", "Candida stomatitis", "Mycotic stomatitis", "candidiasis; mouth", "monilia; stomatitis", "Stomatitis monilial", "stomatitis; mycotic", "Candidosis of mouth", "mycotic; stomatitis", "stomatitis; mycosis", "Moniliasis of mouth", "STOMATITIS MONILIAL", "candidiasis; thrush", "stomatitis; monilia", "Candidal stomatitis", "mycosis; stomatitis", "Candidiasis of mouth", "stomatitis; candidal", "candidiasis of mouth", "candida; thrush, oral", "sprue; candidal, oral", "candidiasis oral thrush", "MOUTH CANDIDA INFECTION", "candidiasis; stomatitis", "Candida infection of mouth", "oral candidiasis (diagnosis)", "Candidiasis of mouth (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oral candidiasis", "shortest_name_length": 6}
{"curie": "UMLS:C1707829", "names": ["Squamoid Ductal Eccrine Carcinoma", "Squamoid Eccrine Ductal Carcinoma", "Ductal Eccrine Carcinoma with Squamous Metaplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Squamoid Eccrine Ductal Carcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C0268877", "names": ["URETHRA CYST", "urethra cyst", "cyst urethra", "Urethra Cyst", "urethral cyst", "cysts urethra", "cyst; urethra", "urethra; cyst", "Urethral cyst", "Urethral Cyst", "cysts urethral", "Cyst of urethra", "Cyst of Urethra", "Cyst of the Urethra", "URETHRAL GLAND, CYST", "urethral cyst (diagnosis)", "Cyst of urethra (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urethral cyst", "shortest_name_length": 12}
{"curie": "MONDO:0001429", "names": ["transient arthropathy", "Transient Arthropathy", "transient arthropathy involving hand", "Transient arthropathy involving hand", "Transient arthropathy, shoulder region", "Transient arthropathy involving forearm", "transient arthropathy involving forearm", "Transient arthropathy of shoulder region", "transient arthropathy involving upper arm", "Transient arthropathy involving upper arm", "Transient arthropathy involving lower leg", "transient arthropathy involving lower leg", "Transient arthropathy of the shoulder region", "Transient arthropathy involving multiple sites", "transient arthropathy involving multiple sites", "transient arthropathy involving shoulder region", "Transient arthropathy involving shoulder region", "Transient arthropathy of shoulder region (disorder)", "transient arthropathy involving pelvic region and thigh", "Transient arthropathy involving pelvic region and thigh"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transient arthropathy", "shortest_name_length": 21}
{"curie": "UMLS:C4524965", "names": ["stage IIB small intestine cancer", "Stage IIB Small Intestinal Adenocarcinoma", "Stage IIB Small Intestinal Adenocarcinoma AJCC v8", "stage IIB small intestinal adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Small Intestinal Adenocarcinoma AJCC v8", "shortest_name_length": 32}
{"curie": "UMLS:C5419068", "names": ["Locally Advanced Oral Cavity Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Oral Cavity Carcinoma", "shortest_name_length": 38}
{"curie": "UMLS:C0238425", "names": ["SICKLE CELL CRISIS", "sickle cell crisis", "Sickle cell crisis", "sickle-cell crisis", "cell crisis sickle", "crisis; sickle-cell", "sickle-cell; crisis", "cells crisis sickle", "Sickle-cell crisis NOS", "sickle cell anemia crisis", "anemia cell crisis sickle", "Hb-SS disease with crisis", "crisis disease hb-s mention", "sickle cell anemia with crisis", "Sickle cell anemia with crisis", "sickle cell crisis (diagnosis)", "Sickle-cell anemia with crisis", "Sickle-cell disease with crisis", "Sickle-cell anaemia with crisis", "Sickle cell anaemia with crisis", "sickle-cell; anemia, with crisis", "anemia; sickle-cell, with crisis", "Hemoglobin S disease with crisis", "Hemoglobin SS disease with crisis", "Haemoglobin S disease with crisis", "sickle-cell; disorder, with crisis", "Haemoglobin SS disease with crisis", "anemia hemolytic sickle cell crisis", "Hb-S disease with mention of crisis", "sickle cell Hb-SS disease with crisis", "Hb-SS disease with crisis, unspecified", "Hb-SS disease with (painful) crisis NOS", "sickle cell anemia with crisis (diagnosis)", "Hemoglobin SS disease with crisis (disorder)", "sickle cell-hemoglobin SS disease with crisis", "disease (or disorder); sickle-cell, with crisis", "sickle cell Hb-SS disease with crisis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemoglobin SS disease with crisis", "shortest_name_length": 18}
{"curie": "MONDO:0005287", "names": ["disorder developmental", "Developmental Disorder", "developmental disorder", "Developmental disorder", "developmental disorders", "DEVELOPMENTAL DISORDERS", "developmental disability", "Developmental Disability", "Developmental disability", "Disability, Developmental", "Developmental disabilities", "Developmental disorder NOS", "Developmental Disabilities", "Child Development Disorder", "developmental disabilities", "child development disorder", "Development Disorder, Child", "Disabilities, Developmental", "Child Development Disorders", "Developmental disorder, NOS", "child development disorders", "Development Disorders, Child", "child; developmental disorder", "developmental disorder; child", "developmental delay disorders", "child developmental disabilities", "Developmental disorder (disorder)", "Developmental disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental disability", "shortest_name_length": 22}
{"curie": "MONDO:0003503", "names": ["fallopian tube squamous cell cancer", "Fallopian Tube Squamous Cell Cancer", "fallopian tube squamous cell carcinoma", "Fallopian Tube Squamous Cell Carcinoma", "Squamous Cell Carcinoma of Fallopian Tube", "squamous cell carcinoma of fallopian tube", "Squamous Cell Carcinoma of the Fallopian Tube", "squamous cell carcinoma of the fallopian tube", "squamous cell carcinoma of fallopian tube (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fallopian tube squamous cell carcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C0017332", "names": ["GENERALIZED NONCONVULSIVE SEIZURE", "generalized nonconvulsive seizure", "Generalised nonconvulsive epilepsy", "Generalized nonconvulsive epilepsy", "Generalized Nonconvulsive Epilepsy", "Generalized non-convulsive epilepsy", "Nonconvulsive Epilepsy, Generalized", "epilepsy generalized non-convulsive", "Generalised non-convulsive epilepsy", "Epilepsy, Generalized Nonconvulsive", "epilepsy; generalized, nonconvulsive", "generalized; epileptic, nonconvulsive", "Generalized nonconvulsive epilepsy, NOS", "SEIZURE DISORDER GENERALIZED NONCONVULSIVE", "Generalized Nonconvulsive Seizure Disorder", "Nonconvulsive Generalized Seizure Disorder", "Seizure Disorder, Generalized Nonconvulsive", "Seizure Disorder, Nonconvulsive Generalized", "Generalized Seizure Disorder, Nonconvulsive", "Nonconvulsive Seizure Disorder, Generalized", "generalized nonconvulsive seizure (diagnosis)", "Generalized non-convulsive epilepsy (disorder)", "Generalized non-convulsive epilepsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Generalized Nonconvulsive Seizure Disorder", "shortest_name_length": 33}
{"curie": "MONDO:0017792", "names": ["Dup(7)(p22.1)", "dup(7)(p22.1)", "trisomy 7p22.1", "Trisomy 7p22.1", "7p22.1 microduplication syndrome", "7p22.1 microduplication syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "7p22.1 microduplication syndrome", "shortest_name_length": 13}
{"curie": "UMLS:C5420862", "names": ["Unresectable Thyroid Gland Oncocytic Carcinoma", "Unresectable Thyroid Gland Hurthle Cell Carcinoma", "Unresectable Thyroid Gland Oncocytic (Hurthle Cell) Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Thyroid Gland Oncocytic Carcinoma", "shortest_name_length": 46}
{"curie": "MONDO:0013508", "names": ["MYP19", "MYOPIA 19, AUTOSOMAL DOMINANT", "myopia 19, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopia 19, autosomal dominant", "shortest_name_length": 5}
{"curie": "UMLS:C5447597", "names": ["Refractory Penile Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Penile Carcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0016842", "names": ["Paternal del(20)(q13.2q13.3)", "paternal del(20)(q13.2q13.3)", "paternal monosomy 20q13.2q13.3", "Paternal monosomy 20q13.2q13.3", "paternal monosomy 20q13.2-q13.3", "paternal 20q13.2q13.3 microdeletion syndrome", "Paternal 20q13.2q13.3 microdeletion syndrome", "paternal 20q13.2-q13.3 microdeletion syndrome", "Paternal 20q13.2q13.3 microdeletion syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paternal 20q13.2q13.3 microdeletion syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0013863", "names": ["CVID8", "LRBA Deficiency", "CID due to LRBA deficiency", "common variable immunodeficiency 8", "combined immunodeficiency due to LRBA deficiency", "Combined immunodeficiency due to LRBA deficiency", "immunodeficiency, common variable, 8, with autoimmunity", "IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY", "Immunodeficiency, Common Variable, 8, with Autoimmunity", "common variable immunodeficiency-8 (CVID8) with autoimmunity", "Combined immunodeficiency due to lipopolysaccharide-responsive beige-like anchor protein deficiency", "Combined immunodeficiency due to lipopolysaccharide-responsive beige-like anchor protein deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined immunodeficiency due to LRBA deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0044334", "names": ["Soft Tissue and Bone Tumor", "soft tissue and bone tumor", "Soft Tissue and Bone Neoplasm", "tumor of soft tissue and bone", "Tumor of Soft Tissue and Bone", "soft tissue and bone neoplasm", "Skeletal and Soft Tissue Tumor", "skeletal and soft tissue tumor", "neoplasm of soft tissue and bone", "Connective and Soft Tissue Tumor", "connective and soft tissue tumor", "Neoplasm of Soft Tissue and Bone", "Tumor of Skeletal and Soft Tissue", "tumor of soft tissue and skeleton", "skeletal and soft tissue neoplasm", "Skeletal and Soft Tissue Neoplasm", "Tumor of Soft Tissue and Skeleton", "tumor of skeletal and soft tissue", "Connective and Soft Tissue Neoplasm", "connective and soft tissue neoplasm", "Neoplasm of Skeletal and Soft Tissue", "neoplasm of skeletal and soft tissue", "neoplasm of soft tissue and skeleton", "Neoplasm of Soft Tissue and Skeleton", "Connective and Soft Tissue Neoplasms", "Neoplasms, Connective and Soft Tissue", "musculoskeletal and soft tissue tumor", "Musculoskeletal and Soft Tissue Tumor", "musculoskeletal and soft tissue neoplasm", "Musculoskeletal and Soft Tissue Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "connective and soft tissue neoplasm", "shortest_name_length": 26}
{"curie": "UMLS:C4764032", "names": ["Recurrent B-Cell Prolymphocytic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent B-Cell Prolymphocytic Leukemia", "shortest_name_length": 40}
{"curie": "MONDO:0009993", "names": ["ERMS", "RMS1", "RMSE1", "RMSCR", "Rhabdomyosarcoma 1", "RHABDOMYOSARCOMA 1", "rhabdomyosarcoma 1", "rhabdomyosarcoma, somatic", "Embryonal Rhabdomyosarcoma", "embryonal rhabdomyosarcoma", "rhabdomyosarcoma embryonal", "Embryonal rhabdomyosarcoma", "rhabdomyosarcoma; embryonal", "embryonal; rhabdomyosarcoma", "Rhabdomyosarcoma, Embryonal", "Embryonal Rhabdomyosarcomas", "Rhabdomyosarcomas, Embryonal", "Rhabdomyosarcoma embryonal 1", "RHABDOMYOSARCOMA, EMBRYONAL, 1", "Rhabdomyosarcoma, Embryonal, 1", "rhabdomyosarcoma, embryonal, 1", "Rhabdomyosarcoma Chromosomal Region", "rhabdomyosarcoma, embryonal, type 1", "rhabdomyosarcoma chromosomal region", "RHABDOMYOSARCOMA CHROMOSOMAL REGION", "embryonal rhabdomyosarcoma (disease)", "Embryonal rhabdomyosarcoma (disorder)", "embryonal rhabdomyosarcoma (diagnosis)", "botryoid rhabdomyosarcoma (type of ERMS)", "spindle cell rhabdomyosarcomas (type of ERMS)", "Embryonal rhabdomyosarcoma (morphologic abnormality)", "malignant neoplasm myosarcoma rhabdomyosarcoma embryonal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "embryonal rhabdomyosarcoma", "shortest_name_length": 4}
{"curie": "MONDO:0014598", "names": ["DEE31", "EIEE31", "DEE31A", "early infantile epileptic encephalopathy 31", "Early Infantile Epileptic Encephalopathy 31", "developmental and epileptic encephalopathy 31", "Developmental and Epileptic Encephalopathy 31", "DNM1 early infantile epileptic encephalopathy", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 31", "epileptic encephalopathy, early infantile, 31", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 31", "developmental and epileptic encephalopathy, 31", "developmental and epileptic encephalopathy 31A", "epileptic encephalopathy, early infantile, type 31", "early infantile epileptic encephalopathy caused by mutation in DNM1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 31", "shortest_name_length": 5}
{"curie": "UMLS:C1504507", "names": ["Bronchial Stricture", "Bronchial stricture", "bronchus; stricture", "stricture; bronchus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bronchial Stricture", "shortest_name_length": 19}
{"curie": "MONDO:0000519", "names": ["corpus callosum oligodendroglioma", "oligodendroglioma of corpus callosum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corpus callosum oligodendroglioma", "shortest_name_length": 33}
{"curie": "MONDO:0017588", "names": ["nail tumor", "tumor of nail", "nail neoplasm", "rare nail tumor", "neoplasm of nail", "nail neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nail tumor", "shortest_name_length": 10}
{"curie": "UMLS:C1334012", "names": ["High Grade Conjunctival Intraepithelial Neoplasia", "High Grade Conjunctival Squamous Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Conjunctival Squamous Intraepithelial Neoplasia", "shortest_name_length": 49}
{"curie": "MONDO:0014413", "names": ["OFD14", "orofaciodigital syndrome 14", "OROFACIODIGITAL SYNDROME XIV", "orofaciodigital syndrome XIV", "C2CD3 orofaciodigital syndrome", "Orofaciodigital syndrome type 14", "orofaciodigital syndrome type 14", "Oro-facial digital syndrome type 14", "oral-facial-digital syndrome type 14", "Oral-facial-digital syndrome type 14", "Oro-facial digital syndrome type 14 (disorder)", "oral-facial-digital syndrome type 14 (diagnosis)", "orofaciodigital syndrome caused by mutation in C2CD3", "microcephaly-cerebral malformation-orofaciodigital syndrome", "Microcephaly-cerebral malformation-orofaciodigital syndrome", "Microcephaly, cerebral malformation, orofaciodigital syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orofaciodigital syndrome type 14", "shortest_name_length": 5}
{"curie": "MONDO:0016532", "names": ["LGS", "Lennox-Gastaut", "Lennox syndrome", "Gastaut syndrome", "gastaut syndrome", "Lennox-Gastat syndrome", "Lennox Gastaut syndrome", "lennox gastaut syndrome", "Lennox-Gastaut Syndrome", "lennox-gastaut syndrome", "Lennox-Gastaut syndrome", "LENNOX-GASTAUT SYNDROME", "lennox gestaut syndrome", "Lennox Gastaut Syndrome", "Lennox-Gestaut syndrome", "lennox-gestaut syndrome", "Lennox Gastaut Syndromes", "encephalopathy of childhood", "Lennox-Gastaut syndrome (disorder)", "Lennox-Gastaut syndrome (diagnosis)", "MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY", "macrocephaly and epileptic encephalopathy", "epileptic encephalopathy Lennox-Gastaut type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lennox-Gastaut syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0004160", "names": ["Female Stress Incontinence", "female incontinence stress", "female stress incontinence", "Female stress incontinence", "stress incontinence female", "Stress incontinence, female", "Stress incontinence - female", "stress incontinence - female", "Female urinary stress incontinence", "female urinary stress incontinence", "female stress incontinence (diagnosis)", "Female urinary stress incontinence (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "female stress incontinence", "shortest_name_length": 26}
{"curie": "MONDO:0017384", "names": ["AGEP", "agep", "Toxic pustuloderma", "toxic pustuloderma", "Pustular drug eruption", "pustular drug eruption", "Acute generalised exanthematous pustulosis", "acute generalized exanthematous pustulosis", "Acute Generalized Exanthematous Pustulosis", "Acute generalized exanthematous pustulosis", "Acute Generalised Exanthematous Pustulosis", "Pustulosis, Exanthematous, Acute Generalized", "AGEP - acute generalized exanthematous pustulosis", "AGEP - acute generalised exanthematous pustulosis", "Acute generalized exanthematous pustulosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute generalized exanthematous pustulosis", "shortest_name_length": 4}
{"curie": "MONDO:0032915", "names": ["LQT16", "CPVT6", "long QT syndrome 16", "LONG QT SYNDROME 16", "VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC 6", "Ventricular Tachycardia, Catecholaminergic Polymorphic 6", "VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "long QT syndrome 16", "shortest_name_length": 5}
{"curie": "MONDO:0017563", "names": ["congenital patella dislocation, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital patella dislocation, bilateral", "shortest_name_length": 41}
{"curie": "MONDO:0014808", "names": ["CSD", "DIAR8", "SLC9A3 secretory diarrhea", "DIARRHEA, CONGENITAL SODIUM", "diarrhea, congenital sodium", "congenital secretory sodium diarrhea 8", "DIARRHEA 8, SECRETORY SODIUM, CONGENITAL", "diarrhea 8, secretory sodium, congenital", "congenital secretory sodium diarrhea type 8", "secretory diarrhea caused by mutation in SLC9A3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital secretory sodium diarrhea 8", "shortest_name_length": 3}
{"curie": "UMLS:C2986691", "names": ["IBMFS", "CBMFS", "Inherited BMF Syndrome", "Inherited BMF Syndromes", "BMF Syndrome, Inherited", "Inherited Bone Marrow Failure Syndrome", "inherited bone marrow failure syndrome", "Inherited bone marrow failure syndrome", "Congenital Bone Marrow Failure Syndrome", "Inherited Bone Marrow Failure Syndromes", "Congenital Bone Marrow Failure Syndromes", "Bone Marrow Failure Syndromes, Inherited", "Bone Marrow Failure Syndromes, Congenital"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Bone Marrow Failure Syndromes", "shortest_name_length": 5}
{"curie": "UMLS:C4521629", "names": ["Stage IVC Sinonasal Cancer AJCC v8", "Stage IVC Sinonasal Carcinoma AJCC v8", "Stage IVC Nasal Cavity and Paranasal Sinus Cancer", "Stage IVC Nasal Cavity and Paranasal Sinus Cancer AJCC v8", "Stage IVC Nasal Cavity and Paranasal Sinus Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Nasal Cavity and Paranasal Sinus Cancer AJCC v8", "shortest_name_length": 34}
{"curie": "UMLS:C1707435", "names": ["Colon TSA", "Colon Serrated Adenoma", "Colon Serrated Adenoma Type II", "Colon Traditional Serrated Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colon Traditional Serrated Adenoma", "shortest_name_length": 9}
{"curie": "MONDO:0008715", "names": ["AFFN dysostosis", "Affn dysostosis 1", "Acrofrontofacionasal dysostosis", "acrofrontofacionasal dysostosis", "Richieri Costa Colletto syndrome", "Richieri-Costa-Colletto syndrome", "acrofrontofacionasal dysostosis 1", "acro fronto facio nasal dysostosis", "Acro fronto facio nasal dysostosis", "Acro-fronto-facio-nasal dysostosis", "acrofrontofacionasal dysostosis type 1", "Acrofrontofacionasal dysostosis syndrome", "acrofrontofacionasal dysostosis syndrome", "Acrofrontofacionasal dysostosis (disorder)", "polysyndactyly, postaxial, frontonasal dysostosis and cleft lip/palate", "polysyndactyly, postaxial, frontonasal dysostosis, and cleft Lip/palate", "cleft Lip/palate with frontonasal dysostosis and postaxial polysyndactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acrofrontofacionasal dysostosis", "shortest_name_length": 15}
{"curie": "MONDO:0003420", "names": ["Bile Duct MCN", "Bile duct cystadenoma", "Bile Duct Cystadenoma", "bile duct cystadenoma", "bile duct; cystadenoma", "cystadenoma; bile duct", "cystadenoma of bile duct", "Cystadenoma of Bile Duct", "cystadenoma of the bile duct", "Cystadenoma of the bile duct", "Cystadenoma of the Bile Duct", "bile duct mucinous cystic neoplasm", "Bile Duct Mucinous Cystic Neoplasm", "bile duct cystadenoma (morphologic abnormality)", "Bile duct cystadenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bile duct cystadenoma", "shortest_name_length": 13}
{"curie": "MONDO:0016911", "names": ["del(13q)", "monosomy 13q", "13q monosomy", "13q deletion", "deletion 13q", "loss of chromosome 13q", "13q- syndrome, partial", "chromosome 13q deletion", "Deletion 13q syndrome, partial", "partial deletion of chromosome 13q", "partial monosomy of chromosome 13q", "partial monosomy of the long arm of chromosome 13", "partial deletion of the long arm of chromosome 13", "partial deletion of the long arm of chromosome type 13"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of the long arm of chromosome 13", "shortest_name_length": 8}
{"curie": "MONDO:0010256", "names": ["MRX21", "MRX34", "XLID21", "X-linked mental retardation 34", "X-linked mental retardation 21", "mental retardation, X-linked 21", "Mental Retardation, X-Linked 21", "Mental Retardation, X-Linked 34", "MENTAL RETARDATION, X-LINKED 34", "mental retardation, X-linked 34", "MENTAL RETARDATION, X-LINKED 21", "Mental retardation, X-linked, 21", "X-linked mental retardation 21/34", "intellectual disability, X-linked 21", "mental retardation, X-linked type 21", "intellectual disability, X-linked 34", "intellectual disability, X-linked type 21", "X-linked mental retardation 21 (MRX21, XLMR21)", "X-linked mental retardation 34 (MRX34. XLMR34)", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 34", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 21", "non-syndromic X-linked intellectual disability 21", "IL1RAPL1 non-syndromic X-linked intellectual disability", "intellectual developmental disorder, X-linked 21, X-linked recessive", "non-syndromic X-linked intellectual disability caused by mutation in IL1RAPL1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 21", "shortest_name_length": 5}
{"curie": "MONDO:0008391", "names": ["ROBINOW-SORAUF SYNDROME", "Robinow-Sorauf Syndrome", "Robinow-Sorauf syndrome", "Robinow Sorauf syndrome", "Craniosynostosis-bifid hallux syndrome", "CRANIOSYNOSTOSIS-BIFID HALLUX SYNDROME", "craniosynostosis-bifid hallux syndrome", "acrocephalosyndactyly, Robinow-Sorauf type", "ACROCEPHALOSYNDACTYLY, ROBINOW-SORAUF TYPE", "Acrocephalosyndactyly, Robinow-Sorauf type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Robinow-Sorauf syndrome", "shortest_name_length": 23}
{"curie": "UMLS:C1332068", "names": ["AJCC G3 Sarcoma", "AJCC Grade 3 Sarcoma", "AJCC Grade III Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AJCC Grade 3 Sarcoma", "shortest_name_length": 15}
{"curie": "MONDO:0008838", "names": ["ADR SYNDROME", "Adr syndrome", "Reardon Baraitser syndrome", "Reardon-Baraitser syndrome", "Reardon Wilson Cavanagh syndrome", "ATAXIA-DEAFNESS-RETARDATION SYNDROME", "ataxia-deafness-retardation syndrome", "Ataxia-deafness-retardation syndrome", "ataxia-deafness-retardation (ADR) syndrome", "Ataxia, hearing loss, and mental retardation", "ataxia, hearing loss, and mental retardation", "Ataxia-deafness-intellectual disability syndrome", "ataxia, hearing loss, and intellectual disability", "familial ataxia, deafness, and developmental delay", "Familial ataxia, deafness, and developmental delay", "ataxia - deafness - intellectual disability syndrome", "ataxia-hearing loss-intellectual disability syndrome", "Ataxia-hearing loss-intellectual disability syndrome", "Ataxia with deafness and intellectual disability syndrome", "Ataxia with deafness and intellectual disability syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ataxia - deafness - intellectual disability syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0002354", "names": ["laryngeal tumor", "larynx neoplasm", "neoplasm of larynx", "benign larynx tumor", "Benign Larynx Tumor", "Benign tumor of larynx", "benign larynx neoplasm", "benign laryngeal tumor", "Benign Tumor of Larynx", "Neoplasm benign;larynx", "benign tumor of larynx", "Benign Laryngeal Tumor", "larynx benign neoplasm", "Benign Larynx Neoplasm", "Larynx neoplasm benign", "LARYNX NEOPLASM BENIGN", "Benign tumour of larynx", "Benign Neoplasm of Larynx", "Benign Laryngeal Neoplasm", "benign laryngeal neoplasm", "benign neoplasm of larynx", "Benign laryngeal neoplasm", "Benign neoplasm of larynx", "laryngeal benign neoplasm", "laryngeal neoplasm, benign", "Benign Tumor of the Larynx", "benign tumor of the larynx", "Laryngeal Neoplasm, Benign", "Benign Neoplasm of the Larynx", "Laryngeal neoplasm benign NOS", "benign neoplasm of the larynx", "Benign neoplasm of larynx, NOS", "Benign neoplasm of larynx (disorder)", "benign neoplasm of larynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign laryngeal neoplasm", "shortest_name_length": 15}
{"curie": "UMLS:C0349204", "names": ["psychosis", "nos psychosis", "Psychosis NOS", "psychosis nos", "Nonorganic psychosis", "nonorganic psychosis", "Non-organic psychosis", "Non-organic psychoses", "psychosis; nonorganic", "non-organic psychosis", "nonorganic origin; psychosis", "non-organic psychotic condition", "Unspecified nonorganic psychosis", "Non-organic psychosis (disorder)", "non-organic psychotic condition (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nonorganic psychosis", "shortest_name_length": 9}
{"curie": "MONDO:0009968", "names": ["DRTA2", "AR dRTA wth deafness", "AR dRTA with hearing loss", "renal tubular acidosis type 1b", "RTA WITH PROGRESSIVE NERVE DEAFNESS", "RTA with progressive nerve deafness", "renal tubular acidosis with deafness", "Renal tubular acidosis with deafness", "renal tubular acidosis progressive nerve deafness", "renal tubular acidosis with progressive nerve deafness", "Renal tubular acidosis with progressive nerve deafness", "Renal Tubular Acidosis with Progressive Nerve Deafness", "RENAL TUBULAR ACIDOSIS WITH PROGRESSIVE NERVE DEAFNESS", "distal renal tubular acidosis with sensorineural deafness", "autosomal recessive distal renal tubular acidosis with deafness", "Autosomal recessive distal renal tubular acidosis with deafness", "renal tubular acidosis, distal, with progressive nerve deafness", "Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness", "Renal tubular acidosis with progressive nerve deafness (disorder)", "renal tubular acidosis with progressive nerve deafness (diagnosis)", "autosomal recessive distal renal tubular acidosis with hearing loss", "distal renal tubular acidosis with sensorineural deafness (diagnosis)", "Distal renal tubular acidosis co-occurrent with sensorineural deafness", "distal renal tubular acidosis co-occurrent with sensorineural deafness", "AR dRTA (autosomal recessive distal renal tubular acidosis) with deafness", "distal renal tubular acidosis 2 with progressive sensorineural hearing loss", "RENAL TUBULAR ACIDOSIS, AUTOSOMAL RECESSIVE, WITH PROGRESSIVE NERVE DEAFNESS", "Renal Tubular Acidosis, Autosomal Recessive, with Progressive Nerve Deafness", "renal tubular acidosis, autosomal recessive, with progressive nerve deafness", "renal tubular acidosis, distal, 2, with progressive sensorineural hearing loss", "RENAL TUBULAR ACIDOSIS, DISTAL, 2, WITH PROGRESSIVE SENSORINEURAL HEARING LOSS", "Distal renal tubular acidosis co-occurrent with sensorineural deafness (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal tubular acidosis, distal, 2, with progressive sensorineural hearing loss", "shortest_name_length": 5}
{"curie": "UMLS:C0152517", "names": ["Viral diarrhea", "viral diarrhea", "Viral vomiting", "diarrhea; viral", "viral; diarrhea", "Viral diarrhoea", "viral diarrhoea", "Diarrhoea;viral", "VIRAL GASTROENTERITIS", "Viral Gastroenteritis", "gastroenteritis viral", "Viral gastroenteritis", "GASTROENTERITIS VIRAL", "Gastroenteritis;viral", "Gastroenteritis viral", "viral gastroenteritis", "GASTROENTERITIS, VIRAL", "gastroenteritis; viral", "viral; gastroenteritis", "Viral gastroenteritis NOS", "Gastroenteritis viral NOS", "Viral gastroenteritis (disorder)", "Enteritis due to specified virus", "enteritis due to specified virus", "viral gastroenteritis (diagnosis)", "enteritis due to specified virus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Viral gastroenteritis", "shortest_name_length": 14}
{"curie": "UMLS:C1832055", "names": ["Hepatic Complication", "hepatic complications"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatic Complication", "shortest_name_length": 20}
{"curie": "UMLS:C2242704", "names": ["Chronic myeloid leukemia transformation", "Chronic myeloid leukaemia transformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic myeloid leukemia transformation", "shortest_name_length": 39}
{"curie": "MONDO:0014639", "names": ["ETL7", "familial temporal lobe epilepsy 7", "epilepsy, familial temporal lobe, 7", "EPILEPSY, FAMILIAL TEMPORAL LOBE, 7", "familial temporal lobe epilepsy type 7", "epilepsy, familial temporal lobe, type 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial temporal lobe epilepsy 7", "shortest_name_length": 4}
{"curie": "MONDO:0017787", "names": ["Leiner disease", "erythroderma desquamativum", "erythroderma desquamativa of Leiner", "Erythroderma desquamativa of Leiner", "erythroderma desquamativum of infancy", "Erythroderma Desquamativum of Infancy", "Leiner-Moussous Desquamative Erythroderma", "Leiner-Moussous desquamative erythroderma", "Generalized erythroderma, diarrhea, and failure to thrive", "generalized erythroderma, diarrhea, and failure to thrive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythroderma desquamativum", "shortest_name_length": 14}
{"curie": "MONDO:0008185", "names": ["HP", "Hp", "HPC", "PCTT", "pancreatitis, chronic", "PANCREATITIS, CHRONIC", "Familial Pancreatitis", "familial pancreatitis", "Calcific pancreatitis", "Pancreatitis, Calcific", "pancreatitis, calcific", "PANCREATITIS, CALCIFIC", "Hereditary Pancreatitis", "hereditary pancreatitis", "Hereditary pancreatitis", "pancreatitis, hereditary", "Pancreatitis, Hereditary", "PANCREATITIS, HEREDITARY", "Familial chronic pancreatitis", "hereditary chronic pancreatitis", "Hereditary Chronic Pancreatitis", "Hereditary chronic pancreatitis", "Hereditary pancreatitis syndrome", "pancreatitis, calcific, included", "Hereditary pancreatitis (disorder)", "Familial chronic pancreatitis (disorder)", "PANCREATITIS, CHRONIC, SUSCEPTIBILITY TO", "pancreatitis, chronic, susceptibility to", "PANCREATITIS, CHRONIC, PROTECTION AGAINST", "pancreatitis, chronic, protection against", "autosomal dominant hereditary pancreatitis", "hereditary chronic pancreatitis (diagnosis)", "pancreatitis, chronic, protection against, included", "Familial pancreatitis with increased cancer syndrome", "pancreatitis, chronic pancreatitis, chronic, susceptibility to, included"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary chronic pancreatitis", "shortest_name_length": 2}
{"curie": "UMLS:C5206510", "names": ["EBV-Related Sarcoma", "EBV-Associated Sarcoma", "Epstein-Barr Virus-Related Sarcoma", "Epstein-Barr Virus-Associated Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "EBV-Related Sarcoma", "shortest_name_length": 19}
{"curie": "UMLS:C5237219", "names": ["Unresectable Triple-Negative Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Triple-Negative Breast Carcinoma", "shortest_name_length": 45}
{"curie": "UMLS:C0751324", "names": ["Multiple Sclerosis, Acute Fulminating"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Multiple Sclerosis, Acute Fulminating", "shortest_name_length": 37}
{"curie": "MONDO:0012722", "names": ["Dauwerse Peters Syndrome", "Dauwerse-Peters syndrome", "DAUWERSE-PETERS SYNDROME", "short stature, facial dysmorphism, severe brachydactyly and syndactyly", "SHORT STATURE, FACIAL DYSMORPHISM, SEVERE BRACHYDACTYLY, AND SYNDACTYLY", "Short Stature, Facial Dysmorphism, Severe Brachydactyly, and Syndactyly", "short stature, Facial Dysmorphism, Severe brachydactyly, and syndactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dauwerse-Peters syndrome", "shortest_name_length": 24}
{"curie": "MONDO:0005780", "names": ["HPS", "Hanta virus", "Hantavirus disease", "Hantavirus Infection", "hantavirus infection", "Hantavirus infection", "HANTAVIRUS INFECTION", "hantavirus infections", "Hantaan virus disease", "infections hantavirus", "Hantavirus Infections", "Hantavirus infections", "infections, Hantavirus", "Infections, Hantavirus", "disease due to hantavirus", "Orthohantavirus Infection", "Disease due to Hantavirus", "Disease due to Hantanvirus", "Orthohantavirus Infections", "Infections, Orthohantavirus", "Disease due to Hantaanvirus", "DISEASES DUE TO HANTANVIRUS", "disease caused by hantavirus", "Disease caused by Hantavirus", "Hantavirus infectious disease", "Disease caused by Hantanvirus", "hantavirus infectious disease", "Hantavirus disease or disorder", "Disease caused by Hantaanvirus", "Hantavirus disease (diagnosis)", "Disease due to Hantanvirus, NOS", "Disease due to Hataanvirus, NOS", "Disease due to Hantaanvirus, NOS", "Hantavirus caused disease or disorder", "Disease caused by Hantavirus (disorder)", "Disease caused by Hantanvirus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hantavirus infectious disease", "shortest_name_length": 3}
{"curie": "MONDO:0009084", "names": ["Jackson-Barr syndrome", "Jackson Barr syndrome", "deafness conductive ptosis skeletal anomalies", "Deafness conductive ptosis skeletal anomalies", "conductive deafness-ptosis-skeletal anomalies syndrome", "Conductive deafness-ptosis-skeletal anomalies syndrome", "DEAFNESS, CONDUCTIVE, WITH PTOSIS AND SKELETAL ANOMALIES", "Deafness, Conductive, with Ptosis and Skeletal Anomalies", "Conductive deafness, ptosis, skeletal anomalies syndrome", "deafness, conductive, with ptosis and skeletal anomalies", "Conductive hearing loss-ptosis-skeletal anomalies syndrome", "Conductive deafness, ptosis, skeletal anomalies syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "conductive deafness-ptosis-skeletal anomalies syndrome", "shortest_name_length": 21}
{"curie": "UMLS:C0158281", "names": ["Cervicobrachial syndrome", "CERVICOBRACHIAL SYNDROME", "cervicobrachial syndrome", "cervicobrachial; syndrome", "syndrome; cervicobrachial", "Diffuse cervicobrachial syndrome", "diffuse cervicobrachial syndrome", "Cervicobrachial syndrome (diffuse)", "Diffuse cervicobrachial syndrome (disorder)", "diffuse cervicobrachial syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervicobrachial syndrome", "shortest_name_length": 24}
{"curie": "UMLS:C0862490", "names": ["Metastatic Endometrioid Carcinoma", "Endometrioid adenocarcinoma metastatic", "Metastatic Endometrioid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endometrioid adenocarcinoma metastatic", "shortest_name_length": 33}
{"curie": "UMLS:C3495847", "names": ["IRIS associated TB", "Immune reconstitution inflammatory syndrome associated tuberculosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immune reconstitution inflammatory syndrome associated tuberculosis", "shortest_name_length": 18}
{"curie": "MONDO:0019953", "names": ["mega-cisterna magna"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mega-cisterna magna", "shortest_name_length": 19}
{"curie": "MONDO:0100424", "names": ["AML, NRAS gene mutation", "AML, N-RAS Gene Mutation", "acute myeloid leukemia, NRAS gene mutation", "AML, Neuroblastoma RAS Viral Oncogene Homolog Gene Mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, NRAS gene mutation", "shortest_name_length": 23}
{"curie": "UMLS:C0038941", "names": ["Incision infection", "INCISIONAL INFECTION", "incisional infection", "Incisional infection", "incisional infections", "Surgical Site Infection", "post-op wound infection", "Infected surgical wound", "Infection;wound;post-op", "Surgical site infection", "Infection, Surgical Site", "Surgical Site Infections", "surgical wound infection", "infection surgical wound", "Surgical wound infection", "infected surgical wounds", "Surgical Wound Infection", "Infection, Surgical Wound", "Wound, surgical, infected", "Infections, Surgical Site", "Surgical wound infections", "infection surgical wounds", "Wound Infection, Surgical", "Surgical Wound Infections", "surgical wound infections", "infection; wound, surgical", "wound; infection, surgical", "infections surgical wounds", "Wound Infections, Surgical", "Infections, Surgical Wound", "operation wound; infection", "infection; operation wound", "Postoperative wound infection", "Postoperative Wound Infection", "postoperative wound infection", "POST-OPERATIVE WOUND INFECTION", "infection; postoperative wound", "Wound Infection, Postoperative", "postoperative wound infections", "Post Operative Wound Infection", "Infection, Postoperative Wound", "postoperative wound; infection", "wound infection; postoperative", "Postoperative Wound Infections", "postoperative; wound infection", "Wound Infections, Postoperative", "Infections, Postoperative Wound", "Surgical site infection (disorder)", "Post procedural site wound infection", "Postoperative wound infection (disorder)", "postoperative wound infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Surgical Wound Infection", "shortest_name_length": 18}
{"curie": "MONDO:0011238", "names": ["brachytelephalangic chondrodysplasia punctata", "chondrodysplasia punctata, brachytelephalangic, autosomal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chondrodysplasia punctata, brachytelephalangic, autosomal", "shortest_name_length": 45}
{"curie": "MONDO:0017696", "names": ["GSDIV, non progressive hepatic form", "GSD type 4, non progressive hepatic form", "GBE deficiency, non progressive hepatic form", "glycogenosis type 4, non progressive hepatic form", "glycogenosis type IV, non progressive hepatic form", "glycogen storage disease type 4, non progressive hepatic form", "glycogen storage disease type IV, non progressive hepatic form", "GSD due to glycogen branching enzyme deficiency, non progressive hepatic form", "glycogenosis due to glycogen branching enzyme deficiency, non progressive hepatic form", "glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form", "shortest_name_length": 35}
{"curie": "MONDO:0044067", "names": ["Invasive Candidiases", "Invasive Candidiasis", "Invasive candidiasis", "invasive candidiasis", "invasive candidiases", "candidiasis, invasive", "Candidiasis, Invasive", "Candidiases, Invasive", "candidiases, invasive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "candidiasis, invasive", "shortest_name_length": 20}
{"curie": "MONDO:0100296", "names": ["PPKM1", "OLMS1", "Olmsted syndrome", "Olmsted syndrome 1", "OLMSTED SYNDROME 1", "autosomal dominant Olmsted syndrome", "palmoplantar keratoderma, mutilating, with periorificial keratotic plaques 1", "PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTIC PLAQUES 1", "autosomal dominant mutilating palmoplantar keratoderma with periorificial keratotic plaques"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Olmsted syndrome 1", "shortest_name_length": 5}
{"curie": "UMLS:C0393560", "names": ["vascular dementia acute onset", "Acute Onset Vascular Dementia", "acute onset vascular dementia", "Vascular Dementia, Acute Onset", "dementia; vascular, acute onset", "vascular; dementia, acute onset", "Vascular dementia of acute onset", "acute onset vascular dementia (diagnosis)", "Vascular dementia of acute onset (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vascular Dementia, Acute Onset", "shortest_name_length": 29}
{"curie": "MONDO:0012074", "names": ["MADB", "mandibuloacral dysplasia type B lipodystrophy", "MANDIBULOACRAL dysplasia with type B lipodystrophy", "Mandibuloacral dysplasia with type B lipodystrophy", "mandibuloacral dysplasia with type B lipodystrophy", "MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY", "LIPODYSTROPHY, TYPE B, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA", "Lipodystrophy, type B, associated with mandibuloacral dysplasia", "lipodystrophy, type B, associated with Mandibuloacral dysplasia", "Mandibuloacral dysostosis co-occurrent with type B lipodystrophy", "Mandibuloacral dysostosis co-occurrent with type B lipodystrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mandibuloacral dysplasia with type B lipodystrophy", "shortest_name_length": 4}
{"curie": "MONDO:0020775", "names": ["Cdgf", "CDGF", "CDGF1", "congenital disorder of glycosylation with defective fucosylation 1", "CONGENITAL DISORDER OF GLYCOSYLATION WITH DEFECTIVE FUCOSYLATION 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital disorder of glycosylation with defective fucosylation 1", "shortest_name_length": 4}
{"curie": "MONDO:0024550", "names": ["FMD", "Fmd", "FMD1", "FRONTOMETAPHYSEAL DYSPLASIA 1", "frontometaphyseal dysplasia 1", "FRONTOMETAPHYSEAL dysplasia 1", "FLNA frontometaphyseal dysplasia", "frontometaphyseal dysplasia 1, X-linked recessive", "frontometaphyseal dysplasia caused by mutation in FLNA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontometaphyseal dysplasia 1", "shortest_name_length": 3}
{"curie": "MONDO:0011589", "names": ["MCOPCB2", "microphthalmia with coloboma 2", "MICROPHTHALMIA, COLOBOMATOUS, ISOLATED 2", "Microphthalmia, Colobomatous, Isolated 2", "microphthalmia, colobomatous, isolated 2", "MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 2", "Microphthalmia, Isolated, with Coloboma 2", "microphthalmia, isolated, with coloboma 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microphthalmia with coloboma 2", "shortest_name_length": 7}
{"curie": "UMLS:C5206605", "names": ["Paratesticular Hemangioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paratesticular Hemangioma", "shortest_name_length": 25}
{"curie": "MONDO:0011397", "names": ["ADCADN", "ADCA-DN", "ADCA-DN syndrome", "autosomal dominant cerebellar ataxia, deafness and narcolepsy", "Autosomal dominant cerebellar ataxia, deafness, and narcolepsy", "autosomal dominant cerebellar ataxia, deafness, and narcolepsy", "CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT", "cerebellar ataxia, deafness, and narcolepsy, autosomal dominant", "autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome", "autosomal dominant cerebellar ataxia, deafness, and narcolepsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant cerebellar ataxia, deafness and narcolepsy", "shortest_name_length": 6}
{"curie": "MONDO:0012117", "names": ["CDGIl", "CDG1L", "CDG 1L", "CDG-IL", "CDG IL", "CDG Il", "ALG9-CDG", "ALG9-CDG (CDG-IL)", "CDG syndrome type IL", "mannosyltransferase 7-9 deficiency", "Mannosyltransferase 7-9 deficiency", "congenital disorder of glycosylation Il", "congenital disorder of glycosylation 1l", "ALG9 congenital disorder of glycosylation", "ALG9-congenital disorder of glycosylation", "congenital disorder of glycosylation type 1L", "Congenital disorder of glycosylation type 1L", "Congenital disorder of glycosylation type IL", "congenital disorder of glycosylation type IL", "Congenital Disorder of Glycosylation, Type IL", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Il", "congenital disorder of glycosylation, type IL", "Carbohydrate deficient glycoprotein syndrome type IL", "carbohydrate deficient glycoprotein syndrome type 1L", "carbohydrate deficient glycoprotein syndrome type IL", "Asparagine-linked glycosylation 9 congenital disorder of glycosylation", "ALG9-CDG - asparagine-linked glycosylation 9 congenital disorder of glycosylation", "Asparagine-linked glycosylation 9 congenital disorder of glycosylation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ALG9-congenital disorder of glycosylation", "shortest_name_length": 5}
{"curie": "MONDO:0003210", "names": ["iCC", "ICC", "iCCA", "ICCA", "IHCH", "peripheral cholangiocarcinoma", "peripheral Cholangiocarcinoma", "Intrahepatic cholangiocarcinoma", "Intrahepatic Cholangiocarcinoma", "intrahepatic cholangiocarcinoma", "Intrahepatic bile duct carcinoma", "intrahepatic bile duct carcinoma", "Intrahepatic Cholangiocarcinomas", "Cholangiocarcinoma, Intrahepatic", "Intrahepatic Bile Duct Carcinoma", "Cholangiocarcinomas, Intrahepatic", "Intrahepatic Carcinoma of Bile Duct", "intrahepatic carcinoma of bile duct", "carcinoma of intrahepatic bile duct", "Intrahepatic Carcinoma of the Bile Duct", "intrahepatic carcinoma of the bile duct", "intrahepatic Cholangiocellular carcinoma", "Intrahepatic Cholangiocellular Carcinoma", "Intrahepatic bile duct carcinoma (disorder)", "cholangiocarcinoma, intrahepatic, malignant", "CHOLANGIOCARCINOMA, INTRAHEPATIC, MALIGNANT", "cholangiocarcinoma of intrahepatic bile duct", "carcinoma of intrahepatic bile duct (diagnosis)", "Cholangiocarcinoma of intrahepatic biliary tract", "Intrahepatic Bile Duct Cancer (Cholangiocarcinoma)", "intrahepatic cholangiocarcinoma (bile duct cancer)", "intrahepatic bile duct cancer (cholangiocarcinoma)", "cholangiocarcinoma of intrahepatic bile duct (diagnosis)", "Cholangiocarcinoma of intrahepatic biliary tract (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intrahepatic cholangiocarcinoma", "shortest_name_length": 3}
{"curie": "MONDO:0004966", "names": ["gastritis", "Gastritis", "GASTRITIS", "Gastritides", "Gastritis NOS", "Gastritis, NOS", "Gastric catarrh", "Stomach inflamed", "Erosive Gastritis", "erosive gastritis", "Erosive gastritis", "Gastritis erosive", "gastritis erosive", "GASTRITIS EROSIVE", "Erosive gastropathy", "erosive gastropathy", "Catarrhal gastritis", "gastritis (disease)", "Gastric inflammation", "gastric inflammation", "STOMACH INFLAMMATION", "Gastritis (disorder)", "Stomach inflammation", "Inflammation;stomach", "stomach inflammation", "Inflammation stomach", "GASTRIC INFLAMMATION", "INFLAMMATION STOMACH", "Hemorrhagic gastritis", "acute gastric erosion", "Erosion;gastric;acute", "gastritis (diagnosis)", "gastritis hemorrhagic", "hemorrhagic gastritis", "Acute gastric erosions", "acute gastric erosions", "Haemorrhagic gastritis", "haemorrhagic gastritis", "Gastritis, unspecified", "acute erosive gastritis", "Acute erosive gastritis", "inflammation of stomach", "Acute erosion of stomach", "erosion (acute) of stomach", "Acute hemorrhagic gastritis", "acute hemorrhagic gastritis", "inflammation of the stomach", "Acute haemorrhagic gastritis", "Erosive gastritis (disorder)", "Acute gastric mucosal erosion", "Erosive gastritis (diagnosis)", "acute gastric mucosal erosion", "Erosive gastropathy (disorder)", "Acute gastric mucosal erosion, NOS", "Acute erosive gastritis (disorder)", "acute erosive gastritis (diagnosis)", "Idiopathic erosive/hemorrhagic gastritis", "Acute gastric mucosal erosion (disorder)", "Idiopathic erosive/haemorrhagic gastritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastritis", "shortest_name_length": 9}
{"curie": "MONDO:0020427", "names": ["Laubry-Pezzi syndrome", "Laubry Pezzi syndrome", "VSD with aortic insufficiency", "Laubry Pezzi syndrome (disorder)", "Laubry-Pezzi syndrome (diagnosis)", "ventricular septal defect Laubry-Pezzi syndrome", "Ventricular septal defect with aortic insufficiency", "ventricular septal defect with aortic insufficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laubry-Pezzi syndrome", "shortest_name_length": 21}
{"curie": "MONDO:0010037", "names": ["sodium pump sites, number of", "sodium-potassium-ATPase activity of red cell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sodium-potassium-ATPase activity of red cell", "shortest_name_length": 28}
{"curie": "UMLS:C4527055", "names": ["Merkel Cell Carcinoma by AJCC v8 Stage", "Neuroendocrine Carcinoma of the Skin by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Merkel Cell Carcinoma by AJCC v8 Stage", "shortest_name_length": 38}
{"curie": "UMLS:C0014558", "names": ["FIT UNCINATE", "Fit uncinate", "uncinate fit", "Uncinate fits", "uncinate fits", "UNCINATE FITS", "Uncinate Epilepsy", "uncinate epilepsy", "epilepsy; uncinate", "Epilepsy, Uncinate", "Uncinate Epilepsies", "uncinate; epileptic", "Epilepsies, Uncinate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uncinate Epilepsy", "shortest_name_length": 12}
{"curie": "MONDO:0030483", "names": ["IMD88", "IMMUNODEFICIENCY 88", "immunodeficiency 88", "IMMUNODEFICIENCY 88, MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE", "Mendelian susceptibility to mycobacterial diseases due to TBX21 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 88", "shortest_name_length": 5}
{"curie": "MONDO:0015714", "names": ["secondary central precocious puberty"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary central precocious puberty", "shortest_name_length": 36}
{"curie": "UMLS:C5205701", "names": ["Head and Neck Large Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Head and Neck Large Cell Neuroendocrine Carcinoma", "shortest_name_length": 49}
{"curie": "UMLS:C4521715", "names": ["Stage I Esophageal Adenocarcinoma", "Postneoadjuvant Therapy Stage I Esophageal Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postneoadjuvant Therapy Stage I Esophageal Adenocarcinoma AJCC v8", "shortest_name_length": 33}
{"curie": "UMLS:C0020903", "names": ["illusion", "ILLUSION", "Illusion", "illusions", "Illusions", "Illusion, NOS", "Illusions (finding)", "illusion perception", "Illusions (Perception)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Illusions", "shortest_name_length": 8}
{"curie": "UMLS:C5556809", "names": ["Refractory Primary Systemic Anaplastic Large Cell Lymphoma, ALK-Positive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Primary Systemic Anaplastic Large Cell Lymphoma, ALK-Positive", "shortest_name_length": 72}
{"curie": "MONDO:0007762", "names": ["HLP type 5", "Type V lipidemia", "Type V Lipidemia", "Type V lipidaemia", "hyperlipemia mixed", "Mixed hyperlipemia", "mixed hyperlipemia", "Mixed Hyperlipemia", "Hyperlipemia, Mixed", "hyperlipemia, mixed", "HYPERLIPEMIA, MIXED", "Mixed Hyperlipemias", "major hyperlipidemia", "Hyperlipemias, Mixed", "Type V hyperlipidemia", "hyperlipidemia type V", "Type V Hyperlipidemia", "Hyperlipidemia, Type V", "hyperlipidemia, type 5", "Type V hyperlipidaemia", "Type V Hyperlipidemias", "HYPERLIPIDEMIA, TYPE V", "Hyperlipidemias, Type V", "familial APOA5 deficiency", "type V hyperlipoproteinemia", "HYPERLIPOPROTEINEMIA TYPE V", "Type V hyperlipoproteinemia", "Fredrickson type V lipaemia", "Hyperlipoproteinemia Type V", "Hyperlipoproteinemia Type 5", "hyperlipoproteinemia type V", "Type V Hyperlipoproteinemia", "hyperlipoproteinemia type 5", "Fredrickson Type V Lipidemia", "Hyperlipoproteinemia Type 5s", "hyperlipoproteinemia, type V", "hyperlipoproteinemia, type 5", "HYPERLIPOPROTEINEMIA, TYPE V", "Type V Hyperlipoproteinemias", "Type V hyperlipoproteinaemia", "Hyperlipoproteinemia, Type V", "Fredrickson Type V lipidemia", "Hyperlipoproteinemias, Type V", "Fredrickson Type V lipidaemia", "Hyperchylomicronemia Late Onset", "Late-Onset Hyperchylomicronemia", "hyperchylomicronemia late onset", "Hyperchylomicronemia, Late Onset", "hyperchylomicronemia, late-onset", "HYPERCHYLOMICRONEMIA, LATE-ONSET", "Hyperchylomicronemia Late Onsets", "Late-Onset Hyperchylomicronemias", "Hyperchylomicronemia, Late-Onset", "Fredrickson type V hyperlipidemia", "Hyperchylomicronemias, Late-Onset", "Familial type V hyperlipoproteinemia", "familial hyperlipoproteinemia type V", "Familial type 5 hyperlipoproteinemia", "familial type 5 hyperlipoproteinemia", "familial apolipoprotein A5 deficiency", "Familial type 5 hyperlipoproteinaemia", "familial apolipoprotein a5 deficiency", "Familial type V hyperlipoproteinaemia", "familial apolipoprotein A-V deficiency", "Fredrickson type V hyperlipoproteinemia", "hyperlipoproteinemia type V (diagnosis)", "Fredrickson; type V hyperlipoproteinemia", "Fredrickson type V hyperlipoproteinaemia", "hyperlipoproteinemia; Fredrickson type V", "Hyperlipoproteinemia, Frederickson type V", "Fredrickson type V hyperlipidemia (diagnosis)", "Familial type 5 hyperlipoproteinemia (disorder)", "HYPERPREBETALIPOPROTEINEMIA WITH CHYLOMICRONEMIA", "hyperlipemia combined fat and carbohydrate-induced", "Hyperlipemia, Combined Fat And Carbohydrate Induced", "Hyperlipemia, Combined Fat And Carbohydrate-Induced", "hyperlipemia, combined fat and carbohydrate-induced", "HYPERLIPEMIA, COMBINED FAT AND CARBOHYDRATE-INDUCED", "Hyperchylomicronemia With Hyperprebetalipoproteinemia, Familial", "hyperchylomicronemia with Hyperprebetalipoproteinemia, familial", "HYPERCHYLOMICRONEMIA WITH HYPERPREBETALIPOPROTEINEMIA, FAMILIAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperlipoproteinemia type V", "shortest_name_length": 10}
{"curie": "UMLS:C4744984", "names": ["Advanced Gastric Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Gastric Neuroendocrine Carcinoma", "shortest_name_length": 41}
{"curie": "UMLS:C5206802", "names": ["Locally Advanced Gastroesophageal Junction Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Gastroesophageal Junction Adenocarcinoma", "shortest_name_length": 57}
{"curie": "UMLS:C0267821", "names": ["Liver congestion", "HEPATIC CONGESTION", "hepatic congestion", "Hepatic congestion", "Hepatic congestion (disorder)", "hepatic congestion (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatic congestion", "shortest_name_length": 16}
{"curie": "UMLS:C3897519", "names": ["Stage IVA Thyroid Gland Follicular Cancer", "Stage IVA Thyroid Gland Follicular Carcinoma", "Stage IVA Thyroid Gland Follicular Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Thyroid Gland Follicular Carcinoma AJCC v7", "shortest_name_length": 41}
{"curie": "UMLS:C4721924", "names": ["stage IB uterine sarcoma", "Stage IB Uterine Sarcoma", "Stage IB Uterine Sarcoma AJCC v7", "stage IB uterine sarcoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Uterine Sarcoma AJCC v7", "shortest_name_length": 24}
{"curie": "MONDO:0006908", "names": ["Pituitary apoplexy", "Pituitary Apoplexy", "pituitary apoplexy", "Apoplexy, Pituitary", "pituitary gland apoplexy", "Pituitary Gland Apoplexy", "Pituitary tumor apoplexy", "Pituitary apoplexy (disorder)", "pituitary apoplexy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pituitary apoplexy", "shortest_name_length": 18}
{"curie": "UMLS:C4525084", "names": ["Colorectal Cancer by AJCC v8 Stage", "Colorectal Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Cancer by AJCC v8 Stage", "shortest_name_length": 34}
{"curie": "UMLS:C4521816", "names": ["Stage IVB Appendix Cancer", "Stage IVB Appendix Carcinoma AJCC v8", "Stage IVB Appendiceal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Appendix Carcinoma AJCC v8", "shortest_name_length": 25}
{"curie": "MONDO:0018629", "names": ["Stiff leg syndrome", "focal stiff limb syndrome", "focal stiff-person syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal stiff limb syndrome", "shortest_name_length": 18}
{"curie": "UMLS:C0311242", "names": ["cyst; gingiva", "Gingival cyst", "gingiva; cyst", "Gingival Cyst", "cyst gingival", "gingival cyst", "Gingival cysts", "gingival cysts", "Gingival odontogenic cyst", "gingival cyst (diagnosis)", "Cyst, gingival odontogenic", "Gingival odontogenic cyst (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gingival odontogenic cyst", "shortest_name_length": 13}
{"curie": "UMLS:C1396635", "names": ["Endometrial Metaplasia", "Endometrial metaplasia", "metaplasia; endometrial", "endometrium; metaplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endometrial metaplasia", "shortest_name_length": 22}
{"curie": "MONDO:0043775", "names": ["diaphragm paralysis", "Paralyzed diaphragm", "Paralysed diaphragm", "diaphragm; paralysis", "paralysis; diaphragm", "RESPIRATORY PARALYSIS", "respiratory paralysis", "Respiratory Paralysis", "Respiratory paralysis", "paralysis of diaphragm", "Paralysis, Respiratory", "paralysis, respiratory", "paralysis; respiratory", "Paralysis of diaphragm", "Diaphragmatic Paralysis", "diaphragmatic paralysis", "Diaphragmatic paralysis", "DIAPHRAGMATIC PARALYSIS", "paralysis, diaphragmatic", "Paralysis, Diaphragmatic", "Respiratory Muscle Paralysis", "respiratory muscle paralysis", "Muscle Paralyses, Respiratory", "Muscle Paralysis, Respiratory", "Paralysis, Respiratory Muscle", "muscle paralyses, respiratory", "paralysis, respiratory muscle", "muscle paralysis, respiratory", "Paralysis of diaphragm (disorder)", "diaphragmatic paralysis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "respiratory paralysis", "shortest_name_length": 19}
{"curie": "MONDO:0019449", "names": ["lissencephaly type 3-familial fetal akinesia sequence syndrome", "Lissencephaly type 3-familial fetal akinesia sequence syndrome", "Lissencephaly type 3 familial fetal akinesia sequence syndrome", "Lissencephaly type 3 familial foetal akinesia sequence syndrome", "Lissencephaly type 3 familial fetal akinesia sequence syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lissencephaly type 3-familial fetal akinesia sequence syndrome", "shortest_name_length": 62}
{"curie": "UMLS:C1522058", "names": ["coagulation necrosis", "Coagulation necrosis", "Coagulative necrosis", "coagulative necrosis", "Coagulative Necrosis", "Necrosis, coagulative", "Coagulative necrosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Coagulative necrosis", "shortest_name_length": 20}
{"curie": "MONDO:0005628", "names": ["Ca breast - male", "Male Breast Tumor", "Male breast cancer", "breast cancer male", "Tumor, Male Breast", "Carcinoma;breast;M", "Breast Tumor, Male", "Breast cancer male", "Male Breast Cancer", "Male Breast Tumors", "cancer male breast", "male breast cancer", "Breast Tumors, Male", "Tumors, Male Breast", "breast cancer, male", "Cancer, Male Breast", "breast cancer males", "Breast Cancer, Male", "Breast cancer, male", "BREAST NEOPLASM MALE", "Male Breast Neoplasm", "breast cancer in men", "Breast neoplasm male", "Tumors, Breast, Male", "of male breast cancer", "Breast Neoplasm, Male", "Male breast carcinoma", "Neoplasm, Male Breast", "male breast carcinoma", "breast carcinoma male", "Cancer of male breast", "Male Breast Neoplasms", "Male Breast Carcinoma", "Breast cancer male NOS", "Neoplasms, Male Breast", "Breast Neoplasms, Male", "Breast Carcinoma, Male", "Carcinoma, Male Breast", "neoplasm of male breast", "Neoplasms, Breast, Male", "carcinoma of the breast", "BREAST, MALE, CARCINOMA", "Neoplasm malig;breast:M", "Neoplasm of male breast", "carcinoma of Male breast", "carcinoma of male breast", "Carcinoma of Male Breast", "Breast neoplasm NOS male", "Carcinoma of male breast", "breast cancer carcinoma male", "Carcinoma of the Male Breast", "carcinoma of the Male breast", "Malignant breast neoplasm male", "malignant tumor of male breast", "Breast neoplasm malignant male", "BREAST NEOPLASM MALIGNANT MALE", "malignant male breast neoplasm", "BREAST, MALE, CANCER, CARCINOMA", "Malignant neoplasm of male breast", "malignant neoplasm of male breast", "Neoplasm of male breast (disorder)", "Carcinoma of male breast (disorder)", "Carcinoma of male breast (diagnosis)", "malignant neosplasm of the male breast", "Malignant neoplasm of male breast, NOS", "breast neoplasm malignant male carcinoma", "Malignant neoplasm of male breast (disorder)", "malignant neoplasm of male breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "male breast carcinoma", "shortest_name_length": 16}
{"curie": "MONDO:0001353", "names": ["Bordetella parapertussis infection", "infection; Bordetella parapertussis", "Whooping cough due to B. parapertussis", "Bordetella parapertussis whooping cough", "infection due to Bordetella parapertussis", "Infection due to Bordetella parapertussis", "Bordetella parapertussis infectious disease", "Bordetella parapertussis disease or disorder", "Infection caused by Bordetella parapertussis", "infection caused by Bordetella parapertussis", "Whooping cough due to bordetella parapertussis", "Whooping cough due to Bordetella parapertussis", "Bordetella parapertussis caused disease or disorder", "Infection due to Bordetella parapertussis (disorder)", "Infection due to Bordetella parapertussis (diagnosis)", "parapertussis; Bordetella parapertussis, whooping cough", "Infection caused by Bordetella parapertussis (disorder)", "Whooping cough due to bordetella parapertussis [B. parapertussis]", "Whooping cough due to bordetella parapertussis (B. parapertussis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bordetella parapertussis infectious disease", "shortest_name_length": 34}
{"curie": "UMLS:C2981402", "names": ["Stage IIIB Colorectal Cancer", "Stage IIIB Colorectal Cancer AJCC v7", "Stage IIIB Colorectal (Colon or Rectal) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Colorectal Cancer AJCC v7", "shortest_name_length": 28}
{"curie": "MONDO:0002833", "names": ["fallopian tube transitional cell cancer", "Fallopian Tube Transitional Cell Cancer", "fallopian tube transitional cell carcinoma", "Fallopian Tube Transitional Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fallopian tube transitional cell carcinoma", "shortest_name_length": 39}
{"curie": "MONDO:0002048", "names": ["immune thrombocytopenia", "Immune thrombocytopenia", "Immune Thrombocytopenia", "Auto-immune thrombocytopenia", "auto-immune thrombocytopenia", "ITP - immune thrombocytopenia", "Immune-mediated thrombocytopenia", "Immune thrombocytopenia (disorder)", "Thrombocytopenia due to immune destruction", "thrombocytopenia due to immune destruction", "Thrombocytopenia Due to Immune Destruction", "Thrombocytopenia due to immune destruction, NOS", "Thrombocytopenia due to platelet alloimmunization", "thrombocytopenia due to platelet alloimmunization", "Thrombocytopenia (due to): platelet alloimmunization", "Thrombocytopenia due to enhanced destruction, immune", "thrombocytopenia due to platelet alloimmunization (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombocytopenia due to immune destruction", "shortest_name_length": 23}
{"curie": "MONDO:0032764", "names": ["3KS", "3K Syndrome", "3K SYNDROME", "Khan-Khan-Katsanis syndrome", "KHAN-KHAN-KATSANIS SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Khan-Khan-Katsanis syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0010832", "names": ["BBS3", "BARDET-BIEDL SYNDROME 3", "Bardet-Biedl syndrome 3", "Bardet-Biedl syndrome type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bardet-Biedl syndrome 3", "shortest_name_length": 4}
{"curie": "UMLS:C2168282", "names": ["Bladder Leiomyosarcoma", "leiomyosarcoma of bladder", "leiomyosarcoma of bladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leiomyosarcoma of bladder", "shortest_name_length": 22}
{"curie": "UMLS:C0270149", "names": ["perinatal respiratory distress", "Perinatal Respiratory Distress", "Perinatal respiratory distress, NOS", "perinatal respiratory distress (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "perinatal respiratory distress", "shortest_name_length": 30}
{"curie": "OMIM:270350", "names": ["ANOSMIA FOR BUTYL MERCAPTAN", "SKUNK N-BUTYL MERCAPTAN, INABILITY TO SMELL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 27}
{"curie": "UMLS:C3160830", "names": ["Prostatic dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostatic dysplasia", "shortest_name_length": 19}
{"curie": "MONDO:0013623", "names": ["BDPLT11", "GP 6 deficiency", "GP VI deficiency", "GP VI DEFICIENCY", "glycoprotein 6 deficiency", "Glycoprotein VI deficiency", "glycoprotein VI deficiency", "GLYCOPROTEIN VI DEFICIENCY", "platelet-type bleeding disorder-11", "platelet-type bleeding disorder 11", "Bleeding disorder platelet-type 11", "bleeding disorder, platelet-type, 11", "BLEEDING DISORDER, PLATELET-TYPE, 11", "GP6 inherited bleeding disorder, platelet-type", "Bleeding disorder due to glycoprotein VI deficiency", "Bleeding diathesis due to glycoprotein VI deficiency", "bleeding diathesis due to glycoprotein VI deficiency", "Bleeding disorder due to glycoprotein VI deficiency (disorder)", "Bleeding disorder due to glycoprotein VI deficiency (diagnosis)", "inherited bleeding disorder, platelet-type caused by mutation in GP6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "platelet-type bleeding disorder 11", "shortest_name_length": 7}
{"curie": "UMLS:C0393561", "names": ["Subcortical vascular dementia", "Subcortical Vascular Dementia", "Subcortical Vascular Dementias", "Dementia, Subcortical Vascular", "Vascular Dementia, Subcortical", "vascular dementia, subcortical", "dementia; vascular, subcortical", "Vascular Dementias, Subcortical", "Dementias, Subcortical Vascular", "vascular; dementia, subcortical", "Subcortical vascular dementia (disorder)", "Subcortical vascular dementia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subcortical Vascular Dementia", "shortest_name_length": 29}
{"curie": "MONDO:0007279", "names": ["CCA1", "CTRCT7", "cataract 7", "cataract type 7", "Cerulean type cataract 7", "cerulean type cataract 7", "cataract 7, cerulean type", "congenital Cerulean type cataract 1", "congenital cerulean type cataract 1", "cataract, congenital, cerulean type, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 7", "shortest_name_length": 4}
{"curie": "UMLS:C1518702", "names": ["Ovarian Dermoid Cyst with Prolactin Secreting Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Dermoid Cyst with Prolactin Secreting Adenoma", "shortest_name_length": 53}
{"curie": "MONDO:0015347", "names": ["MR", "MRH", "Nicolau-Balus syndrome", "LIPOID DERMATOARTHRITIS", "Lipoid dermatoarthritis", "lipoid dermatoarthritis", "HISTIOCYTOMA, GIANT CELL", "Lipoid dermato-arthritis", "Giant cell histiocytomatosis", "giant cell histiocytomatosis", "Lipoid dermatoarthritis (disorder)", "RETICULOHISTIOCYTOMA, MULTICENTRIC", "Multicentric reticulohistiocytosis", "multicentric reticulohistiocytosis", "Multicentric Reticulohistiocytosis", "lipoid dermatoarthritis (diagnosis)", "lipoid metabolism disorder lipoid dermatoarthritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multicentric reticulohistiocytosis", "shortest_name_length": 2}
{"curie": "UMLS:C0333880", "names": ["Glandular cell atypia", "Glandular Cell Atypia", "Glandular cell atypia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Glandular cell atypia", "shortest_name_length": 21}
{"curie": "MONDO:0030307", "names": ["SPGF55", "spermatogenic failure 55", "SPERMATOGENIC FAILURE 55"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 55", "shortest_name_length": 6}
{"curie": "UMLS:C1335359", "names": ["Parotid Kaposi's Sarcoma", "Kaposi's Sarcoma of Parotid", "Parotid Gland Kaposi Sarcoma", "Parotid Gland Kaposi's Sarcoma", "Kaposi's Sarcoma of the Parotid", "Kaposi's Sarcoma of Parotid Gland", "Kaposi's Sarcoma of the Parotid Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parotid Gland Kaposi Sarcoma", "shortest_name_length": 24}
{"curie": "UMLS:C0016427", "names": ["follicle cyst", "cyst follicle", "Follicle cyst", "FOLLICULAR CYST", "Follicular Cyst", "follicular cyst", "Follicular cyst", "Follicular Cysts", "follicular; cyst", "cyst; follicular", "Cyst, Follicular", "follicular cysts", "Cyst, follicular", "Cysts, Follicular", "Follicular cyst, NOS", "Hair follicular cyst", "Cyst of hair follicle", "Cyst of hair follicle (finding)", "Follicular cyst (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Follicular cyst", "shortest_name_length": 13}
{"curie": "MONDO:0007420", "names": ["DDOD", "Ddod syndrome", "DDOD Syndrome", "DDOD syndrome", "DDOD SYNDROME", "Robinson Miller Bensimon syndrome", "Robinson-Miller-Bensimon syndrome", "deafness and onychodystrophy, dominant form", "DDOD (dominant deafness onychodystrophy) syndrome", "autosomal dominant deafness-onychodystrophy syndrome", "Autosomal dominant deafness-onychodystrophy syndrome", "Autosomal Dominant Deafness-onychodystrophy Syndrome", "deafness-onychodystrophy syndrome, autosomal dominant", "autosomal dominant deafness - onychodystrophy syndrome", "Autosomal dominant hearing loss-onychodystrophy syndrome", "Autosomal dominant hearing loss, onychodystrophy syndrome", "Autosomal dominant deafness with onychodystrophy syndrome", "Autosomal Dominant Congenital Deafness with Onychodystrophy", "autosomal dominant congenital deafness with onychodystrophy", "Deafness, Congenital, and Onychodystrophy, Autosomal Dominant", "deafness, congenital, and onychodystrophy, autosomal dominant", "deafness, congenital, with onychodystrophy, autosomal dominant", "DEAFNESS, CONGENITAL, WITH ONYCHODYSTROPHY, AUTOSOMAL DOMINANT", "Autosomal dominant deafness with onychodystrophy syndrome (disorder)", "familial ectodermal dysplasia with sensori-neural deafness and other anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant deafness - onychodystrophy syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0012250", "names": ["CMT4H", "Charcot-Marie-Tooth disease type 4H", "Charcot-Marie-Tooth disease type 4h", "Charcot-Marie-Tooth disease, type 4H", "CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H", "Charcot-Marie-Tooth Disease, Type 4H", "Charcot-Marie-Tooth neuropathy type 4H", "Charcot-Marie-Tooth Neuropathy, Type 4H", "FGD4 Charcot-Marie-Tooth disease type 4", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4H", "Charcot-Marie-Tooth neuropathy, type 4H", "Charcot-Marie-Tooth disease type 4H (disorder)", "Charcot-Marie-Tooth disease type 4h (diagnosis)", "autosomal recessive Charcot-Marie-Tooth disease type 4H", "CHARCOT-MARIE-TOOTH DISEASE, AUTOSOMAL RECESSIVE, TYPE 4H", "Charcot-Marie-Tooth Disease, Autosomal Recessive, Type 4H", "Charcot-Marie-Tooth disease, autosomal recessive, type 4H", "Charcot-Marie-Tooth disease type 4 caused by mutation in FGD4", "autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4H", "Charcot-Marie-Tooth Disease, Demyelinating, Autosomal Recessive, Type 4H", "CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, AUTOSOMAL RECESSIVE, TYPE 4H", "Charcot-Marie-Tooth disease, demyelinating, autosomal recessive, type 4H"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 4H", "shortest_name_length": 5}
{"curie": "UMLS:C0751340", "names": ["myasthenia ocular", "Ocular myasthenia", "ocular myasthenia", "gravis myasthenia ocular", "ocular myasthenia gravis", "Ocular Myasthenia Gravis", "Myasthenia Gravis, Ocular", "Ocular myasthenia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myasthenia Gravis, Ocular", "shortest_name_length": 17}
{"curie": "UMLS:C2749515", "names": ["Collapsing glomerulopathy", "Collapsing Glomerulopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Collapsing glomerulopathy", "shortest_name_length": 25}
{"curie": "UMLS:C0333442", "names": ["Hydropic Change", "hydropic change", "Hydropic change", "changes hydropic", "Molar degeneration", "molar degeneration", "Hydropic degeneration", "hydropic degeneration", "Degeneration, hydropic", "Colliquative degeneration", "Hydatidiform degeneration", "Liquefactive degeneration", "Degeneration, liquefactive", "Hydropic degeneration (diagnosis)", "Hydropic degeneration (morphologic abnormality)", "pregnancy abnormal product of conception hydropic degeneration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hydropic degeneration", "shortest_name_length": 15}
{"curie": "UMLS:C5236089", "names": ["Advanced Malignant PEComa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Malignant PEComa", "shortest_name_length": 25}
{"curie": "MONDO:0700139", "names": ["Canine Neoplasm", "canine neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canine neoplasm", "shortest_name_length": 15}
{"curie": "MONDO:0004020", "names": ["Mediastinal Grey Zone Lymphoma", "mediastinal Gray zone lymphoma", "mediastinal gray zone lymphoma", "Mediastinal Gray Zone Lymphoma", "mediastinal B-cell lymphoma, unclassifiable, with features Intermediate between diffuse large B-cell lymphoma and Classic Hodgkin lymphoma", "Mediastinal B-Cell Lymphoma, Unclassifiable, with Features Intermediate between Diffuse Large B-Cell Lymphoma and Classic Hodgkin Lymphoma", "mediastinal B-cell lymphoma, unclassifiable, with features Intermediate between diffuse large B-cell lymphoma and classical Hodgkin lymphoma", "Mediastinal B-Cell Lymphoma, Unclassifiable, with Features Intermediate between Diffuse Large B-Cell Lymphoma and Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mediastinal gray zone lymphoma", "shortest_name_length": 30}
{"curie": "MONDO:0000986", "names": ["pleurisy", "PLEURISY", "Pleurisy", "pleuritis", "Pleuritis", "PLEURITIS", "pleurisies", "Pleurisies", "Pleuritides", "Pleurisy NOS", "Pleurisy, NOS", "Pleuritis, NOS", "Pleurisy (excl TB)", "Pleurisy (disorder)", "pleura inflammation", "pleurisy (diagnosis)", "inflammation of pleura", "Inflammation of pleura", "Pleurisy (excluding TB)", "Inflammation of tissues lining lungs and chest", "Other specified forms of pleural effusion, except tuberculous"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pleurisy", "shortest_name_length": 8}
{"curie": "MONDO:0001547", "names": ["Atrophic nonflaccid tympanic membrane", "atrophic nonflaccid tympanic membrane", "Atrophic nonflaccid tympanic membrane (disorder)", "atrophic nonflaccid tympanic membrane (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrophic nonflaccid tympanic membrane", "shortest_name_length": 37}
{"curie": "UMLS:C5419180", "names": ["COVID-19-Associated Acute Kidney Injury", "SARS-CoV-2-Associated Acute Kidney Injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "COVID-19-Associated Acute Kidney Injury", "shortest_name_length": 39}
{"curie": "UMLS:C1141940", "names": ["rejection; transplant, bowel", "Intestine transplant rejection", "intestine transplant; rejection", "Rejection of intestine transplant", "Rejection of intestine transplant (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rejection of intestine transplant", "shortest_name_length": 28}
{"curie": "MONDO:0020316", "names": ["CBFB-MYH11", "acute myelomonocytic leukemia", "AML with inv(16)(p13.1q22) or t(16;16)(p13.1;q22)", "AML with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)", "acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)", "shortest_name_length": 10}
{"curie": "UMLS:C2984113", "names": ["Hypopharyngeal Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypopharyngeal Carcinoma by AJCC v7 Stage", "shortest_name_length": 41}
{"curie": "UMLS:C1697750", "names": ["Spermatic cord stenosis", "Spermatic Cord Stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spermatic cord stenosis", "shortest_name_length": 23}
{"curie": "MONDO:0019792", "names": ["ADCA1", "ADCAI", "cerebellar plus syndrome", "autosomal dominant cerebellar ataxia type 1", "autosomal dominant cerebellar ataxia type I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant cerebellar ataxia type I", "shortest_name_length": 5}
{"curie": "UMLS:C4725708", "names": ["Body Cavity PEL", "Body Cavity Primary Effusion Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Body Cavity Primary Effusion Lymphoma", "shortest_name_length": 15}
{"curie": "MONDO:0100345", "names": ["Alactasia", "Hypolactasia", "Milk intolerance", "milk intolerance", "Milk Intolerance", "MILK INTOLERANCE", "milk; intolerance", "intolerance; milk", "Lactose intolerance", "Intolerance to milk", "LACTOSE INTOLERANCE", "lactase persistence", "Intolerance;lactose", "lactose intolerance", "INTOLERANCE LACTOSE", "Lactose Intolerance", "Intolerance, Lactose", "intolerance; lactose", "lactose; intolerance", "Lactose Malabsorption", "Cows milk enteropathy", "Lactose malabsorption", "MILK SUGAR INTOLERANCE", "cow's milk enteropathy", "Intolerance to lactose", "Malabsorption, Lactose", "lactose; malabsorption", "malabsorption; lactose", "Milk Sugar Intolerance", "Dairy Product Intolerance", "Dairy product intolerance", "LM - lactose malabsorption", "milk; intolerance, lactose", "LM - Lactose malabsorption", "intolerance; milk, lactose", "Intolerance to milk (finding)", "lactose intolerance (disease)", "Lactose intolerance, unspecified", "Intolerance to lactose (finding)", "Intolerance or malabsorption of lactose"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lactose intolerance", "shortest_name_length": 9}
{"curie": "UMLS:C5555721", "names": ["Ovarian Mixed Germ Cell-Sex Cord-Stromal Tumor, Unclassified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Mixed Germ Cell-Sex Cord-Stromal Tumor, Unclassified", "shortest_name_length": 60}
{"curie": "MONDO:0016187", "names": ["qualitative or quantitative defects of desmin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of desmin", "shortest_name_length": 45}
{"curie": "MONDO:0004089", "names": ["BPSCC", "penis basaloid carcinoma", "Basaloid Carcinoma of Penis", "basaloid carcinoma of penis", "basaloid carcinoma of the penis", "Basaloid Carcinoma of the Penis", "penis basaloid squamous cell carcinoma", "basaloid carcinoma of penis (diagnosis)", "basaloid penile squamous cell carcinoma", "Basaloid Penile Squamous Cell Carcinoma", "Basaloid Squamous Cell Carcinoma of Penis", "basaloid squamous cell carcinoma of penis", "basaloid squamous cell carcinoma of the penis", "Basaloid Squamous Cell Carcinoma of the Penis", "Squamous Cell Carcinoma of Penis, Basaloid Type", "squamous cell carcinoma of penis, basaloid type", "squamous cell carcinoma of penis, Basaloid type", "squamous cell carcinoma of the penis, basaloid type", "Squamous Cell Carcinoma of the Penis, Basaloid Type", "basaloid squamous cell carcinoma of penis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "basaloid carcinoma of the penis", "shortest_name_length": 5}
{"curie": "UMLS:C1334661", "names": ["Mediastinal Lipoma", "mediastinal lipoma", "lipoma of mediastinum", "Lipoma of Mediastinum", "Lipoma of the Mediastinum", "lipoma of mediastinum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lipoma of mediastinum", "shortest_name_length": 18}
{"curie": "MONDO:0015776", "names": ["CDPR", "RCDP", "rhizomelic dwarfism", "Rhizomelic Dwarfism", "rhizomelic chondrodysplasia punctata", "Rhizomelic Chondrodysplasia Punctata", "Rhizomelic chondrodysplasia punctata", "Rhizomelic chrondrodysplasia punctata", "Punctata, Rhizomelic Chondrodysplasia", "Rhizomelic Chondrodysplasia Punctatas", "Chondrodysplasia Punctata, Rhizomelic", "Chondrodysplasia Punctatas, Rhizomelic", "Punctatas, Rhizomelic Chondrodysplasia", "Chondrodysplasia punctata, rhizomelic type", "CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC FORM", "chondrodysplasia punctata, rhizomelic form", "Chondrodysplasia Punctata, Rhizomelic Form", "RCDP - Rhizomelic chondrodysplasia punctata", "rhizomelic chondrodysplasia punctata syndrome", "Rhizomelic Chondrodysplasia Punctata Syndrome", "Rhizomelic chondrodysplasia punctata syndrome", "rhizomelic chondrodysplasia punctata (diagnosis)", "Chondrodysplasia punctata, autosomal recessive type", "Rhizomelic chondrodysplasia punctata syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rhizomelic chondrodysplasia punctata", "shortest_name_length": 4}
{"curie": "UMLS:C4727144", "names": ["Refractory Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor", "shortest_name_length": 67}
{"curie": "UMLS:C3805278", "names": ["Extrahepatic Cholangiocarcinoma", "Extrahepatic cholangiocarcinoma", "Extrahepatic Cholangiocarcinomas", "Cholangiocarcinoma, Extrahepatic", "Cholangiocarcinomas, Extrahepatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extrahepatic Cholangiocarcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0043218", "names": ["Neurovascular Disorder", "neurovascular disorder", "vasculature nervous system disorder", "disease of nervous system vasculature", "nervous system disorder of vasculature"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurovascular disorder", "shortest_name_length": 22}
{"curie": "UMLS:C1333117", "names": ["Colorectal Tubular Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Tubular Adenoma", "shortest_name_length": 26}
{"curie": "MONDO:0005213", "names": ["uterus carcinoma", "uterine carcinoma", "Carcinoma of uterus", "carcinoma of uterus", "Malignant epithelial neoplasm of uterus", "Malignant epithelial neoplasm of uterus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine carcinoma", "shortest_name_length": 16}
{"curie": "MONDO:0013272", "names": ["Del(14)(q11.2)", "Monosomy 14q11.2", "monosomy 14q11.2", "ZAHIR-FRIEDMAN SYNDROME", "14q11.2 microdeletion syndrome", "chromosome 14q11-q22 deletion syndrome", "CHROMOSOME 14q11-q22 DELETION SYNDROME", "14q11.2 microdeletion syndrome (disorder)", "chromosome 14q11-q22 deletion syndrome, isolated cases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 14q11-q22 deletion syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0004435", "names": ["liver fibrosarcoma", "Liver Fibrosarcoma", "Hepatic Fibrosarcoma", "hepatic fibrosarcoma", "fibrosarcoma of liver", "Fibrosarcoma of Liver", "Fibrosarcoma of the Liver", "fibrosarcoma of the liver", "liver fibrosarcoma (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "liver fibrosarcoma", "shortest_name_length": 18}
{"curie": "UMLS:C3899120", "names": ["Fetal SGA with Abnormal Doppler", "Fetal SGA with Abnormal Dopplers", "Fetus Small for Gestational Age with Abnormal Doppler", "Fetal Small for Gestational Age with Abnormal Doppler", "Fetal Small for Gestational Age with Abnormal Dopplers"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fetus Small for Gestational Age with Abnormal Doppler", "shortest_name_length": 31}
{"curie": "MONDO:0005167", "names": ["fibroma", "FIBROMA", "Fibroma", "fibromas", "Fibromas", "Fibroma NOS", "Fibroma, NOS", "Fibroma durum", "FIBROMA, BENIGN", "fibroma, benign", "Fibroma (disorder)", "fibrous tissue tumor", "Tumor of fibrous tissue NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibroma", "shortest_name_length": 7}
{"curie": "UMLS:C1708044", "names": ["Fetal Brain Injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fetal Brain Injury", "shortest_name_length": 18}
{"curie": "MONDO:0013572", "names": ["KPLBS", "KEPPEN-Lubinsky syndrome", "KEPPEN-LUBINSKY SYNDROME", "Keppen Lubinsky syndrome", "Keppen-Lubinsky syndrome", "Keppen Lubinsky syndrome (disorder)", "Generalized lipodystrophy-progeroid features-severe intellectual disability syndrome", "generalized lipodystrophy-progeroid features-severe intellectual disability syndrome", "Generalised lipodystrophy, progeroid features, severe intellectual disability syndrome", "Generalized lipodystrophy, progeroid features, severe intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Keppen-Lubinsky syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C1708549", "names": ["Intimal dissection", "Intimal Dissection Of Blood Vessel"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intimal dissection", "shortest_name_length": 18}
{"curie": "MONDO:0002937", "names": ["Rodent Ulcer", "Rodent ulcer", "nodular basal cell carcinoma", "Nodular Basal Cell Carcinoma", "Basal cell carcinoma, nodular", "basal cell carcinoma, nodular", "Skin Nodular Basal Cell Carcinoma", "Nodular Basal Cell Carcinoma of Skin", "Nodular basal cell carcinoma of skin", "nodular basal cell carcinoma of skin", "Nodulo-ulcerative basal cell carcinoma", "Nodulo-Ulcerative Basal Cell Carcinoma", "Skin Nodular Solid Basal Cell Carcinoma", "Nodular Basal Cell Carcinoma of the Skin", "circumscribed solid basal cell carcinoma", "Circumscribed solid basal cell carcinoma", "skin solid (nodular) basal cell carcinoma", "skin solid (nodular) Basal cell carcinoma", "skin nodulo-ulcerative basal cell carcinoma", "Skin Nodulo-Ulcerative Basal Cell Carcinoma", "Nodular basal cell carcinoma of skin (disorder)", "nodular basal cell carcinoma of skin (diagnosis)", "Nodulo-ulcerative basal cell carcinoma (disorder)", "Nodulo-ulcerative basal cell carcinoma (diagnosis)", "Circumscribed solid basal cell carcinoma (disorder)", "Circumscribed solid basal cell carcinoma (diagnosis)", "basal cell carcinoma, nodular (morphologic abnormality)", "skin neoplasm malignant carcinoma basal cell nodulo-ulcerative", "skin neoplasm malignant carcinoma basal cell circumscribed solid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nodular basal cell carcinoma", "shortest_name_length": 12}
{"curie": "MONDO:0035370", "names": ["ALPI-related inflammatory bowel disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ALPI-related inflammatory bowel disease", "shortest_name_length": 39}
{"curie": "UMLS:C0474441", "names": ["Microcystic Edema", "Fine corneal edema", "corneal edema fine", "Fine corneal oedema", "Microcytic Corneal Edema", "Microcystic Corneal Edema", "Corneal microcystic edema", "Microcystic corneal edema", "Microcystic corneal oedema", "Corneal microcystic oedema", "Fine corneal edema (disorder)", "Fine corneal edema (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fine corneal edema", "shortest_name_length": 17}
{"curie": "MONDO:0012046", "names": ["Congenital Corneal Opacities, Cornea Guttata, and Corectopia", "CONGENITAL CORNEAL OPACITIES, CORNEA GUTTATA, AND CORECTOPIA", "congenital corneal opacities, cornea guttata, and corectopia", "Corneal Opacities, Congenital, with Cornea Guttata and Corectopia", "corneal opacities, congenital, with cornea guttata and corectopia", "CORNEAL OPACITIES, CONGENITAL, WITH CORNEA GUTTATA AND CORECTOPIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital corneal opacities, cornea guttata, and corectopia", "shortest_name_length": 60}
{"curie": "MONDO:0011469", "names": ["CAMT", "thrombocytopenia congenital amegakaryocytic", "Congenital Amegakaryocytic Thrombocytopenia", "congenital amegakaryocytic thrombocytopenia", "Congenital amegakaryocytic thrombocytopenia", "Amegakaryocytic Thrombocytopenia, Congenital", "thrombocytopenia, congenital amegakaryocytic", "AMEGAKARYOCYTIC THROMBOCYTOPENIA, CONGENITAL", "amegakaryocytic thrombocytopenia, congenital", "congenital amegakaryocytic thrombocytopenic purpura", "Congenital amegakaryocytic thrombocytopenia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital amegakaryocytic thrombocytopenia", "shortest_name_length": 4}
{"curie": "UMLS:C0078922", "names": ["Tyrosinase-Positive Albinism", "Albinism, tyrosinase positive", "Albinism, Tyrosinase Positive", "Albinism, Tyrosinase-Positive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Albinism, Tyrosinase-Positive", "shortest_name_length": 28}
{"curie": "MONDO:0060577", "names": ["NEDMAS", "neurodevelopmental disorder with microcephaly, ataxia, and seizures", "NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ATAXIA, AND SEIZURES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with microcephaly, ataxia, and seizures", "shortest_name_length": 6}
{"curie": "MONDO:0013549", "names": ["NACED", "NAA DEFICIENCY", "naa deficiency", "hypoacetylaspartia", "HYPOACETYLASPARTIA", "N-acetylaspartate deficiency", "N-ACETYLASPARTATE DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "N-acetylaspartate deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C3203466", "names": ["Acute enterocolitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute enterocolitis", "shortest_name_length": 19}
{"curie": "MONDO:0033537", "names": ["COXPD47", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 47", "combined oxidative phosphorylation deficiency 47"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation deficiency 47", "shortest_name_length": 7}
{"curie": "UMLS:C4744471", "names": ["Hereditary Malignant Urinary System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hereditary Malignant Urinary System Neoplasm", "shortest_name_length": 44}
{"curie": "UMLS:C5238743", "names": ["Hypotension due to cardiac dysfunction", "Hypotension due to Cardiac Dysfunction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypotension due to Cardiac Dysfunction", "shortest_name_length": 38}
{"curie": "UMLS:C0278677", "names": ["Renal cancer stage III", "stage III kidney cancer", "Hypernephroma stage III", "Kidney cancer stage III", "stage III hypernephroma", "kidney cancer, stage III", "hypernephroma, stage III", "Renal carcinoma stage III", "Kidney carcinoma stage III", "Carcinoma kidney stage III", "Stage III renal cell cancer", "stage III renal cell cancer", "Stage III Renal Cell Cancer", "renal cell cancer, stage III", "stage III renal cell carcinoma", "Renal cell carcinoma stage III", "renal cell carcinoma, stage III", "Stage III Renal Cell Cancer AJCC v6", "Renal Cell Cancer Stage III AJCC v6", "Stage III Renal Cell Carcinoma AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III renal cell cancer", "shortest_name_length": 22}
{"curie": "UMLS:C0263264", "names": ["Dermatitis due to acids", "Dermatitis due to Acids", "Contact dermatitis due to acid", "contact dermatitis due to acids", "Contact dermatitis due to acids", "Contact dermatitis caused by acid", "contact dermatitis due to acids (diagnosis)", "Contact dermatitis caused by acid (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Contact dermatitis due to acid", "shortest_name_length": 23}
{"curie": "UMLS:C0238792", "names": ["bone lesion", "Bone lesion", "Lesion;bone", "Bone Lesion", "BONE LESION", "lesion bone", "bone; lesion", "lesion; bone", "bone lesions", "Lesion of bone", "Bone lesion NOS", "Skeletal Lesion", "lesion on the bone", "Lesion of bone (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone lesion", "shortest_name_length": 11}
{"curie": "MONDO:0013267", "names": ["BMIQ16", "BMIQ19", "Distal del(16)(p11.2)", "distal del(16)(p11.2)", "body mass index QTL16", "Distal monosomy 16p11.2", "distal monosomy 16p11.2", "Susceptibility to obesity", "OBESITY, SUSCEPTIBILITY TO", "obesity, susceptibility to", "chromosome 16p11.2 deletion syndrome", "Distal 16p11.2 microdeletion syndrome", "distal 16p11.2 microdeletion syndrome", "chromosome 16p11.2 deletion syndrome, 220kb", "BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 16", "body Mass index quantitative trait locus 16", "BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 19", "chromosome 16p11.2 deletion syndrome, 220-KB", "CHROMOSOME 16p11.2 DELETION SYNDROME, 220-KB", "Distal 16p11.2 microdeletion syndrome (disorder)", "chromosome 16p11.2 deletion syndrome, type 220kb"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal 16p11.2 microdeletion syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C5418902", "names": ["Metastatic Platinum-Resistant Malignant Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Platinum-Resistant Malignant Germ Cell Tumor", "shortest_name_length": 55}
{"curie": "MONDO:0018001", "names": ["inverse Klippel-Trenaunay syndrome", "inverse Klippel-Trénaunay syndrome", "cutaneous hemangioma with muscle or bone atrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inverse Klippel-Trenaunay syndrome", "shortest_name_length": 34}
{"curie": "MONDO:0017215", "names": ["calciphylaxes", "Calciphylaxis", "Calciphylaxes", "calciphylaxis", "Calciphylaxis (disorder)", "Idiopathic Calciphylaxis", "idiopathic calciphylaxis", "Calciphylaxis, Idiopathic", "calciphylaxis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "calciphylaxis", "shortest_name_length": 13}
{"curie": "UMLS:C0854972", "names": ["Stage I Adenosquamous Lung Cancer", "Stage I Adenosquamous Lung Carcinoma", "Adenosquamous cell lung cancer stage I", "Stage I Adenosquamous Cell Lung Carcinoma", "Stage I Adenosquamous Cell Carcinoma of Lung", "Stage I Lung Adenosquamous Carcinoma AJCC v7", "Stage I Adenosquamous Cell Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenosquamous cell lung cancer stage I", "shortest_name_length": 33}
{"curie": "UMLS:C1881058", "names": ["Hodgkin's Disease, Lymphocyte Depletion, Diffuse Fibrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's Disease, Lymphocyte Depletion, Diffuse Fibrosis", "shortest_name_length": 57}
{"curie": "UMLS:C4525732", "names": ["Posterior Subcapsular Cataract Grade 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Posterior Subcapsular Cataract Grade 2", "shortest_name_length": 38}
{"curie": "UMLS:C0399472", "names": ["Ulcerated oral leucoplakia", "Ulcerated Oral Leukoplakia", "Ulcerated oral leukoplakia", "Ulcerated oral leukoplakia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ulcerated oral leukoplakia", "shortest_name_length": 26}
{"curie": "UMLS:C2981694", "names": ["stage IB eyelid carcinoma", "Stage IB Eyelid Carcinoma", "Stage IB Eyelid Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Eyelid Carcinoma AJCC v7", "shortest_name_length": 25}
{"curie": "UMLS:C0340754", "names": ["SUBCLAVIAN VEIN STENOSIS", "Subclavian Vein Stenosis", "Subclavian vein stenosis", "Subclavian vein stenosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subclavian vein stenosis", "shortest_name_length": 24}
{"curie": "MONDO:0032684", "names": ["IMAGEI", "IMAGEI SYNDROME", "Imagei Syndrome", "IMAGE-I syndrome", "intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency", "INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIA CONGENITA, GENITAL ANOMALIES, AND IMMUNODEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency", "shortest_name_length": 6}
{"curie": "UMLS:C0338338", "names": ["Recurrent Cerebellar Astrocytoma", "Relapsed Childhood Cerebellar Astrocytoma", "Relapsed Pediatric Cerebellar Astrocytoma", "Recurrent Childhood Cerebellar Astrocytoma", "recurrent pediatric cerebellar astrocytoma", "recurrent childhood cerebellar astrocytoma", "Recurrent Pediatric Cerebellar Astrocytoma", "childhood cerebellar astrocytoma, recurrent", "pediatric cerebellar astrocytoma, recurrent", "Relapsed Pediatric Astrocytoma of Cerebellum", "cerebellar astrocytoma, pediatric, recurrent", "cerebellar astrocytoma, childhood, recurrent", "Relapsed Childhood Astrocytoma of Cerebellum", "Recurrent Childhood Astrocytoma of Cerebellum", "Recurrent Pediatric Astrocytoma of Cerebellum", "Relapsed Childhood Astrocytoma of the Cerebellum", "Relapsed Pediatric Astrocytoma of the Cerebellum", "Recurrent Childhood Astrocytoma of the Cerebellum", "Recurrent Pediatric Astrocytoma of the Cerebellum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Cerebellar Astrocytoma", "shortest_name_length": 32}
{"curie": "MONDO:0100093", "names": ["FCM", "MYOCL1", "myoclonus, familial, 1", "myoclonus, familial cortical"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myoclonus, familial, 1", "shortest_name_length": 3}
{"curie": "UMLS:C4745064", "names": ["Recurrent Biliary Tract Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Biliary Tract Carcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C5420195", "names": ["Recurrent Mature T-Cell and NK-Cell Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Mature T-Cell and NK-Cell Neoplasm", "shortest_name_length": 44}
{"curie": "MONDO:0016008", "names": ["FHS", "Meadow", "Meadow syndrome", "Dilantin syndrome", "dilantin syndrome", "Meadow's syndrome", "Hydantoin syndrome", "hydantoin syndrome", "Dilantin Embryopathy", "Dilantin embryopathy", "phenytoin embryopathy", "Phenytoin Embryopathy", "fetal dilantin syndrome", "fetal Dilantin syndrome", "fetal hydantoin syndrome", "Fetal Hydantoin Syndrome", "Fetal hydantoin syndrome", "fetal phenytoin syndrome", "Fetal phenytoin syndrome", "FETAL HYDANTOIN SYNDROME", "Foetal hydantoin syndrome", "fetus; hydantoin syndrome", "hydantoin; fetal syndrome", "phenytoin embryofetopathy", "hydantoin syndrome; fetus", "Phenytoin embryofetopathy", "Foetal phenytoin syndrome", "fetal; hydantoin syndrome", "syndrome; fetal, hydantoin", "syndrome; hydantoin, fetal", "Fetal dihydantoin syndrome", "hydantoin; syndrome, fetal", "fetal dihydantoin syndrome", "congenital hydantoin syndrome", "fetal hydantoin syndrome (FHS)", "Fetal hydantoin syndrome (disorder)", "fetal hydantoin syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fetal hydantoin syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0008883", "names": ["Brachydactyly, Type A2, With Microcephaly", "brachydactyly, type A2, with microcephaly", "BRACHYDACTYLY, TYPE A2, WITH MICROCEPHALY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly, type A2, with microcephaly", "shortest_name_length": 41}
{"curie": "MONDO:0018955", "names": ["RRP", "AORRP (type)", "JORRP (type)", "respiratory papillomatosis", "Respiratory papillomatosis", "juvenile laryngeal papilloma", "Juvenile laryngeal papilloma", "Laryngeal papilloma, recurrent", "laryngeal papilloma, recurrent", "Recurrent Respiratory Papillomatosis", "recurrent respiratory papillomatosis", "Recurrent respiratory papillomatosis", "respiratory papillomatosis, recurrent", "Recurrent respiratory papillomatosis (disorder)", "Recurrent respiratory papillomatosis (diagnosis)", "Juvenile-onset recurrent respiratory papillomatosis", "adult-onset recurrent respiratory papillomatosis (type)", "juvenile-onset recurrent respiratory papillomatosis (type)", "benign neoplasm respiratory system recurrent papillomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "recurrent respiratory papillomatosis", "shortest_name_length": 3}
{"curie": "MONDO:0016308", "names": ["Niemann-Pick disease type C, late infantile neurologic onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Niemann-Pick disease type C, late infantile neurologic onset", "shortest_name_length": 60}
{"curie": "MONDO:0006887", "names": ["parametritis", "PARAMETRITIS", "Parametritis", "Parametritides", "Parametritis, NOS", "Pelvic cellulitis", "Pelvic Cellulitis", "pelvic cellulitis", "Cellulitis, Pelvic", "Pelvic Cellulitides", "Cellulitides, Pelvic", "Parametritis (disorder)", "parametrium inflammation", "parametritis (diagnosis)", "inflammation of parametrium", "pelvic cellulitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parametritis", "shortest_name_length": 12}
{"curie": "UMLS:C5238539", "names": ["Recurrent High Risk Chronic Myelomonocytic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent High Risk Chronic Myelomonocytic Leukemia", "shortest_name_length": 51}
{"curie": "MONDO:0003184", "names": ["trachea cancer", "Trachea Cancer", "tracheal cancer", "Trachea--Cancer", "Tracheal cancer", "Pancoast's tumor", "Cancer of Trachea", "cancer of trachea", "Trachea Carcinoma", "Carcinoma;trachea", "trachea carcinoma", "carcinoma trachea", "tracheal carcinoma", "Tracheal Carcinoma", "carcinoma of trachea", "Carcinoma of Trachea", "Cancer of the Trachea", "cancer of the trachea", "carcinoma of the trachea", "Carcinoma of the Trachea", "carcinoma of trachea (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trachea carcinoma", "shortest_name_length": 14}
{"curie": "MONDO:0004816", "names": ["refractory plasma cell neoplasm", "Refractory Plasma Cell Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "refractory plasma cell neoplasm", "shortest_name_length": 31}
{"curie": "MONDO:0800086", "names": ["primary osteodysplasia with multiple joint dislocations", "primary bone dysplasia with multiple joint dislocations", "primary skeletal dysplasia with multiple joint dislocations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary bone dysplasia with multiple joint dislocations", "shortest_name_length": 55}
{"curie": "MONDO:0016379", "names": ["erosive pustular dermatosis of the scalp", "Erosive pustular dermatosis of the scalp", "Erosive pustular dermatosis of the scalp (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erosive pustular dermatosis of the scalp", "shortest_name_length": 40}
{"curie": "MONDO:0006608", "names": ["SEBORRHEA", "Seborrhea", "seborrhea", "seborrhoea", "cradle Cap", "Cradle Cap", "Seborrhoea", "SEBORRHOEA", "Seborrhea NOS", "Seborrhea, NOS", "Seborrhoea, NOS", "skin seborrheic", "Skin seborrheic", "SKIN SEBORRHEIC", "Skin seborrhoeic", "SKIN SEBORRHOEIC", "Eczema seborrheic", "Seborrheic Eczema", "seborrhea; eczema", "seborrheic eczema", "Seborrheic eczema", "ECZEMA, SEBORRHEIC", "seborrhoeic eczema", "Eczema;seborrhoeic", "eczema; seborrheic", "Eczema seborrhoeic", "seborrheic; eczema", "Seborrhoeic eczema", "Seborrheic diathesis", "seborrhea; dermatitis", "SEBORRHEIC DERMATITIS", "DERMATITIS SEBORRHEIC", "seborrhea (diagnosis)", "Seborrheic Dermatitis", "Dermatitis seborrheic", "seborrheic dermatitis", "Seborrheic dermatitis", "dermatitis; seborrhea", "dermatitis seborrheica", "Dermatitis, Seborrheic", "DERMATITIS SEBORRHOEIC", "Dermatitis seborrhoeic", "Dermatitis Seborrheica", "seborrhoeic dermatitis", "Dermatitis;seborrhoeic", "DERMATITIS, SEBORRHEIC", "Seborrhoeic dermatitis", "Seborrheic Dermatitides", "Dysseborrheic dermatitis", "Dermatitides, Seborrheic", "Seborrheic dermatitis NOS", "SBD - Seborrheic dermatitis", "SBD - Seborrhoeic dermatitis", "seborrheic dermatitis (disease)", "Seborrheic dermatitis (disorder)", "seborrheic dermatitis (diagnosis)", "Seborheic dermatitis, unspecified", "Seborrheic dermatitis, unspecified", "Seborrhoeic dermatitis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "seborrheic dermatitis", "shortest_name_length": 9}
{"curie": "MONDO:0007005", "names": ["ulcerative rectosigmoiditis", "Ulcerative rectosigmoiditis", "ulcerative; rectosigmoiditis", "Ulcerative proctosigmoiditis", "rectosigmoiditis; ulcerative", "ulcerative proctosigmoiditis", "ulcerative; proctosigmoiditis", "proctosigmoiditis; ulcerative", "Chronic ulcerative rectosigmoiditis", "Chronic ulcerative proctosigmoiditis", "Ulcerative (chronic) rectosigmoiditis", "Ulcerative (chronic) proctosigmoiditis", "ulcerative rectosigmoiditis (diagnosis)", "ulcerative proctosigmoiditis (diagnosis)", "Ulcerative (chronic) rectosigmoiditis NOS", "Chronic ulcerative rectosigmoiditis (disorder)", "Ulcerative colitis confined to rectum and sigmoid colon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ulcerative proctosigmoiditis", "shortest_name_length": 27}
{"curie": "MONDO:0023655", "names": ["IMD14B", "immunodeficiency 14b, autosomal recessive", "IMMUNODEFICIENCY 14B, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 14b, autosomal recessive", "shortest_name_length": 6}
{"curie": "MONDO:0017891", "names": ["inherited renal cancer-predisposing syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited renal cancer-predisposing syndrome", "shortest_name_length": 44}
{"curie": "UMLS:C4054210", "names": ["Penile chordee", "Penile Chordee"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Penile chordee", "shortest_name_length": 14}
{"curie": "UMLS:C0750905", "names": ["Inherited Errors of Amino Acid Metabolism", "Amino Acid Metabolism, Inherited Disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Amino Acid Metabolism, Inherited Disorders", "shortest_name_length": 41}
{"curie": "UMLS:C4724830", "names": ["Unresectable Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Carcinoma", "shortest_name_length": 22}
{"curie": "MONDO:0009896", "names": ["Infantile polymyoclonus", "polymyoclonus, infantile", "Polymyoclonus, infantile", "POLYMYOCLONUS, INFANTILE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polymyoclonus, infantile", "shortest_name_length": 23}
{"curie": "MONDO:0003785", "names": ["wbc low", "low wbc", "WBC DEC", "WBC LOW", "low wbcs", "leukopenia", "LEUKOPENIA", "Leucopenia", "leucopenia", "Leukopenia", "LEUCOPENIA", "Leukopenias", "wbc decreas", "NEUTROPENIA", "WBC decreased", "WBC DECREASED", "decreased wbc", "Leukocytopenia", "Leukopenia NOS", "leukocytopenia", "Leucocytopenia", "decreasing wbc", "Leucopenia, NOS", "Leukocytopenias", "Leukopenia, NOS", "decreased leukocytes", "LEUKOCYTES DECREASED", "leukocytes decreased", "Leukocytes decreased", "WBC numbers decreased", "Leukopenia (disorder)", "leukopenia (diagnosis)", "Leukocyte count decreased", "Low white blood cell count", "Decreased white cell count", "White blood cell count low", "White blood cell decreased", "low white blood cell count", "Leukocytopenia, unspecified", "white blood cells decreased", "WHITE BLOOD CELLS DECREASED", "decreased white blood cells", "WHITE BLOOD CELL COUNT DECREASED", "Decreased blood leukocyte number", "decreased white blood cell count", "Decreased blood leucocyte number", "Decreased white blood cell count", "White blood cell count decreased", "White blood cell numbers decreased", "white blood cells decreased (lab test)", "Blood leucocyte number below reference range", "Blood leukocyte number below reference range", "Blood leukocyte number below reference range (finding)", "hematology nonspecific abnormal findings white blood cells decreased"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukopenia", "shortest_name_length": 7}
{"curie": "MONDO:0009891", "names": ["PV", "PRV", "p.vera", "p vera", "erythremia", "Erythremia", "ERYTHREMIA", "Erythremias", "erythraemia", "Erythraemia", "Vaquez-Osler", "Osler-Vaquez", "Vaquez disease", "erythrocythemia", "osler's disease", "Vaquez's disease", "vaquez's disease", "Polycythemia Vera", "Polycythemia vera", "polycythemia vera", "Heilmeyer-Schöner", "POLYCYTHEMIA VERA", "polycythaemia vera", "vera; polycythemia", "Polycythaemia vera", "chronic erythremia", "Chronic erythremia", "polycythemia; vera", "chronic; erythremia", "erythremia; chronic", "Chronic erythraemia", "OSLER-VAQUEZ DISEASE", "Osler-Vaquez disease", "Primary polycythemia", "VAQUEZ-OSLER DISEASE", "Osler Vaquez Disease", "primary polycythemia", "Osler-Vaquez Disease", "Primary Polycythemia", "Osler-Vaquez syndrome", "Polycythemia, Primary", "Primary polycythaemia", "Primary Polycythemias", "Disease, Osler-Vaquez", "[M]Chronic erythremia", "POLYCYTHEMIA, PRIMARY", "polycythemia ruba vera", "Polycythemia Ruba Vera", "[M]Chronic erythraemia", "Polycythemias, Primary", "Polycythemia rubra vera", "Polycythemia Rubra Vera", "Ruba Vera, Polycythemia", "Polycythemia Ruba Veras", "POLYCYTHEMIA RUBRA VERA", "polycythemia rubra vera", "Vera, Polycythemia Ruba", "polycythaemia rubra vera", "Polycythemia Rubra Veras", "polycythemia; rubra vera", "Vera, Polycythemia Rubra", "Ruba Veras, Polycythemia", "Veras, Polycythemia Ruba", "Polycythaemia rubra vera", "Heilmeyer-Schoner disease", "Veras, Polycythemia Rubra", "proliferative polycythemia", "polycythemia vera, somatic", "Proliferative polycythemia", "splenomegalic polycythemia", "acquired polycythemia vera", "proliferative polycythaemia", "Proliferative polycythaemia", "Chronic erythremic myelosis", "leukemia chronic erythremia", "POLYCYTHEMIA, SPLENOMEGALIC", "Polycythemia vera (disorder)", "Polycythemia vera (clinical)", "Polycythaemia vera (clinical)", "PRV - Polycythemia rubra vera", "polycythemia vera (diagnosis)", "chronic erythremia (diagnosis)", "rubra; polycythemia rubra vera", "PRV - Polycythaemia rubra vera", "acquired primary erythrocytosis", "Acquired primary erythrocytosis", "Primary proliferative polycythemia", "Primary proliferative polycythaemia", "PPP - Primary proliferative polycythemia", "PPP - Primary proliferative polycythaemia", "Polycythemia vera (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired polycythemia vera", "shortest_name_length": 2}
{"curie": "UMLS:C1096656", "names": ["Cardiac Granuloma", "Cardiac granuloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiac granuloma", "shortest_name_length": 17}
{"curie": "MONDO:0004867", "names": ["upper respiratory disease", "Upper respiratory disease", "diseases respiratory upper", "Upper respiratory disease, NOS", "upper respiratory tract disease", "upper respiratory tract disorder", "upper respiratory tract disorders", "disease of upper respiratory tract", "Disease of upper respiratory tract", "disorder of upper respiratory tract", "Disorder of upper respiratory system", "Disease of upper respiratory tract, NOS", "Disease of upper respiratory system, NOS", "upper respiratory tract disease or disorder", "upper respiratory tract disorders (diagnosis)", "disease or disorder of upper respiratory tract", "Disease of upper respiratory tract, unspecified", "disease (or disorder); respiratory tract, upper", "Disorder of upper respiratory system (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "upper respiratory tract disorder", "shortest_name_length": 25}
{"curie": "UMLS:C5555069", "names": ["Central Chondrosarcoma, Grade 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Chondrosarcoma, Grade 1", "shortest_name_length": 31}
{"curie": "MONDO:0033549", "names": ["OPA12", "OPTIC ATROPHY 12", "optic atrophy 12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "optic atrophy 12", "shortest_name_length": 5}
{"curie": "MONDO:0034991", "names": ["intrauterine growth restriction-congenital multiple café-au-lait macules-increased sister chromatid exchange syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intrauterine growth restriction-congenital multiple café-au-lait macules-increased sister chromatid exchange syndrome", "shortest_name_length": 117}
{"curie": "MONDO:0010385", "names": ["XLP2", "XLP2/XIAP", "XIAP deficiency", "XIAP Deficiency", "Xiap deficiency", "XIAP DEFICIENCY", "XIAP Deficiency/XLPs", "XIAP deficiency/XLPs", "XIAP deficiency syndrome", "X-linked lymphoproliferative syndrome 2", "X-linked Lymphoproliferative Syndrome 2", "lymphoproliferative syndrome, X-linked, 2", "LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 2", "Lymphoproliferative Syndrome, X-Linked, 2", "X-linked lymphoproliferative syndrome type 2", "lymphoproliferative syndrome, X-linked, type 2", "XIAP-related lymphoproliferative disease, X-linked", "X-linked lymphoproliferative disease due to XIAP deficiency", "lymphoproliferative syndrome, X-linked, 2, X-linked recessive", "X-linked lymphoproliferative disease due to XIAP deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked lymphoproliferative disease due to XIAP deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0008961", "names": ["CMT4A", "Charcot Marie Tooth disease type 4A", "Charcot-Marie-Tooth disease Type 4A", "Charcot-Marie-Tooth disease type 4A", "Charcot-Marie-Tooth disease, type 4A", "CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A", "Charcot-Marie-Tooth disease, Type 4A", "Charcot-Marie-Tooth neuropathy type 4A", "Charcot-Marie-Tooth neuropathy, type 4A", "Charcot-Marie-Tooth Neuropathy, Type 4a", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4A", "GDAP1 Charcot-Marie-Tooth disease type 4", "Charcot-Marie-Tooth disease type 4A (disorder)", "Charcot-Marie-Tooth disease Type 4A (diagnosis)", "Charcot-Marie-Tooth disease type 4 caused by mutation in GDAP1", "Charcot-Marie-Tooth disease, demyelinating, autosomal recessive", "autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4A", "CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, AUTOSOMAL RECESSIVE, TYPE 4A", "Charcot-Marie-Tooth disease, demyelinating, autosomal recessive, type 4A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 4A", "shortest_name_length": 5}
{"curie": "MONDO:0003932", "names": ["Visual Pathway Glioma", "visual pathway glioma", "pediatric optic tract glioma", "childhood optic tract glioma", "Childhood Optic Nerve Glioma", "pediatric optic nerve glioma", "childhood optic nerve glioma", "glioma, pediatric optic nerve", "optic tract glioma, childhood", "optic nerve glioma, childhood", "glioma, pediatric optic tract", "glioma, childhood optic nerve", "glioma, childhood optic tract", "optic tract glioma, pediatric", "optic nerve glioma, pediatric", "Optic Nerve Glioma, Childhood", "Glioma, Optic Nerve, Childhood", "pediatric visual pathway glioma", "Pediatric Visual Pathway Glioma", "childhood visual pathway glioma", "optic nerve glioma of childhood", "Childhood Visual Pathway Glioma", "glioma pediatric visual pathway", "glioma, pediatric visual pathway", "glioma, childhood visual pathway", "visual pathway glioma, pediatric", "visual pathway glioma, childhood", "Glioma of Pediatric Visual Pathway", "glioma of pediatric visual pathway", "glioma of childhood visual pathway", "Glioma of Childhood Visual Pathway", "CNS tumor, childhood optic tract gloma", "glioma of the childhood visual pathway", "glioma of the pediatric visual pathway", "Glioma of the Childhood Visual Pathway", "Glioma of the Pediatric Visual Pathway", "childhood CNS tumor, optic tract glioma", "CNS tumor, pediatric optic tract glioma", "pediatric CNS tumor, optic nerve glioma", "childhood CNS tumor, optic nerve glioma", "CNS tumor, childhood optic tract glioma", "CNS tumor, pediatric optic nerve glioma", "CNS tumor, childhood optic nerve glioma", "pediatric CNS tumor, optic tract glioma", "brain tumor, pediatric optic nerve glioma", "brain tumor, childhood optic nerve glioma", "Brain tumor, child: Visual pathway glioma", "pediatric brain tumor, optic nerve glioma", "pediatric brain tumor, optic tract glioma", "childhood brain tumor, optic tract glioma", "brain tumor, pediatric optic tract glioma", "brain tumor, childhood optic tract glioma", "childhood brain tumor, optic nerve glioma", "brain tumor, optic tract glioma, childhood", "brain tumor, optic nerve glioma, childhood", "childhood visual pathway and hypothalamic glioma", "visual pathway and hypothalamic glioma, childhood", "central nervous system tumor, optic tract glioma, childhood", "central nervous system tumor, optic nerve glioma, childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood optic nerve glioma", "shortest_name_length": 21}
{"curie": "MONDO:0022650", "names": ["cardiomyopathy diabetes deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiomyopathy diabetes deafness", "shortest_name_length": 32}
{"curie": "UMLS:C0334390", "names": ["Acinar cell tumor", "acinar cell tumor", "acinic cell tumor", "Acinic cell tumor", "Acinar Cell Tumor", "Acinic cell tumour", "Acinar cell tumour", "acinic cell; tumor", "tumor; acinic cell", "Acinar Cell Neoplasm", "Acinar cell neoplasm", "ACINAR CELL NEOPLASMS", "Acinar Cell Neoplasms", "Acinar cell neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acinar cell tumor", "shortest_name_length": 17}
{"curie": "MONDO:0002703", "names": ["Appendix Colloid Cystadenocarcinoma", "appendix colloid cystadenocarcinoma", "Mucinous cystadenocarcinoma appendix", "Appendix Mucinous Cystadenocarcinoma", "appendix mucinous cystadenocarcinoma", "Appendix Colloidal Cystadenocarcinoma", "appendix colloidal cystadenocarcinoma", "Appendiceal Colloid Cystadenocarcinoma", "Colloid Cystadenocarcinoma of Appendix", "appendiceal colloid cystadenocarcinoma", "colloid cystadenocarcinoma of appendix", "Appendiceal Mucinous Cystadenocarcinoma", "appendiceal mucinous cystadenocarcinoma", "mucinous cystadenocarcinoma of appendix", "Mucinous Cystadenocarcinoma of Appendix", "Appendiceal Colloidal Cystadenocarcinoma", "colloidal cystadenocarcinoma of appendix", "appendiceal colloidal cystadenocarcinoma", "Colloidal Cystadenocarcinoma of Appendix", "Colloid Cystadenocarcinoma of the Appendix", "colloid cystadenocarcinoma of the appendix", "mucinous cystadenocarcinoma of the appendix", "Mucinous Cystadenocarcinoma of the Appendix", "colloidal cystadenocarcinoma of the appendix", "Colloidal cystadenocarcinoma of the appendix", "Colloidal Cystadenocarcinoma of the Appendix", "vermiform appendix mucinous cystadenocarcinoma", "mucinous cystadenocarcinoma of appendix (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "appendix mucinous cystadenocarcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C3272852", "names": ["Anal NET G1", "Anal Canal NET G1", "Anal Carcinoid Tumor", "Anal Canal Carcinoid Tumor", "Anal Neuroendocrine Tumor G1", "Anal Canal NET G1 (Carcinoid)", "Carcinoid Tumor of the Anal Canal", "Anal Canal Neuroendocrine Tumor G1", "Anal Neuroendocrine Tumor G1 (Carcinoid)", "Anal Canal Neuroendocrine Tumor G1 (Carcinoid)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anal Canal Neuroendocrine Tumor G1", "shortest_name_length": 11}
{"curie": "MONDO:0014607", "names": ["DEE32", "EIEE32", "early infantile epileptic encephalopathy 32", "Early Infantile Epileptic Encephalopathy 32", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 32", "Developmental and Epileptic Encephalopathy 32", "epileptic encephalopathy, early infantile, 32", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 32", "developmental and epileptic encephalopathy 32", "KCNA2 early infantile epileptic encephalopathy", "developmental and epileptic encephalopathy, 32", "epileptic encephalopathy, early infantile, type 32", "early infantile epileptic encephalopathy caused by mutation in KCNA2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 32", "shortest_name_length": 5}
{"curie": "MONDO:0002301", "names": ["frontal sinus epidermoid carcinoma", "Frontal Sinus Epidermoid Carcinoma", "frontal sinus squamous cell carcinoma", "epidermoid carcinoma of frontal sinus", "Frontal Sinus Squamous Cell Carcinoma", "Epidermoid Carcinoma of Frontal Sinus", "Squamous Cell Carcinoma of Frontal Sinus", "Squamous cell carcinoma of frontal sinus", "squamous cell carcinoma of frontal sinus", "Epidermoid Carcinoma of the Frontal Sinus", "epidermoid carcinoma of the frontal sinus", "Epidermoid carcinoma of the Frontal sinus", "squamous cell carcinoma of the frontal sinus", "Squamous Cell Carcinoma of the Frontal Sinus", "Primary squamous cell carcinoma of frontal sinus", "Squamous cell carcinoma of frontal sinus (disorder)", "Squamous cell carcinoma of frontal sinus (diagnosis)", "Primary squamous cell carcinoma of frontal sinus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontal sinus squamous cell carcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0014347", "names": ["SSMCF", "short stature with microcephaly and distinctive facies", "SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short stature with microcephaly and distinctive facies", "shortest_name_length": 5}
{"curie": "MONDO:0014757", "names": ["TKS", "TAKENOUCHI-Kosaki syndrome", "Takenouchi-Kosaki syndrome", "TAKENOUCHI-KOSAKI SYNDROME", "Takenouchi Kosaki syndrome", "macrothrombocytopenia and mental retardation syndrome", "MACROTHROMBOCYTOPENIA AND MENTAL RETARDATION SYNDROME", "macrothrombocytopenia and intellectual disability syndrome", "Macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome", "macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome", "Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome", "Macrothrombocytopenia, lymphoedema, developmental delay, facial dysmorphism, camptodactyly syndrome", "Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C1336856", "names": ["Anaplastic Extrahepatic Bile Duct Carcinoma", "anaplastic carcinoma of extrahepatic bile duct", "Anaplastic Carcinoma of Extrahepatic Bile Duct", "Undifferentiated Extrahepatic Bile Duct Carcinoma", "Extrahepatic Bile Duct Undifferentiated Carcinoma", "Anaplastic Carcinoma of the Extrahepatic Bile Duct", "undifferentiated carcinoma of extrahepatic bile duct", "Undifferentiated Carcinoma of Extrahepatic Bile Duct", "Undifferentiated Carcinoma of the Extrahepatic Bile Duct", "anaplastic carcinoma of extrahepatic bile duct (diagnosis)", "undifferentiated carcinoma of extrahepatic bile duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anaplastic carcinoma of extrahepatic bile duct", "shortest_name_length": 43}
{"curie": "MONDO:0018997", "names": ["Noonan", "noonan syndrome", "Noonan Syndrome", "Noonan syndrome", "NOONAN SYNDROME", "noonans syndrome", "Noonan's Syndrome", "noonan's syndrome", "Noonan's syndrome", "Turner-like syndrome", "Turner-Like Syndrome", "male turner syndrome", "Turner Like Syndrome", "Noonan-Ehmke syndrome", "Noonan Ehmke Syndrome", "Noonan-Ehmke Syndrome", "PSEUDO-TURNER SYNDROME", "males syndrome turners", "Ullrich-Noonan Syndrome", "Ullrich-Noonan syndrome", "Ullrich Noonan Syndrome", "familial Turner syndrome", "Familial Turner Syndrome", "familial syndrome turners", "Turner Syndrome, Familial", "Noonan's syndrome (disorder)", "Noonan's syndrome (diagnosis)", "Pseudo-Ullrich-Turner Syndrome", "Pseudo Ullrich Turner Syndrome", "pseudo-Ullrich-Turner syndrome", "Turner phenotype, karyotype normal", "Turner's Phenotype, Karyotype Normal", "Turner's phenotype, karyotype normal", "Turner phenotype with normal karyotype", "TURNER PHENOTYPE WITH NORMAL KARYOTYPE", "Turner Phenotype with Normal Karyotype", "Turner syndrome in female with X chromosome", "Turner's phenotype, karyotype normal (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Noonan syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C2981693", "names": ["Stage IA Eyelid Carcinoma", "Stage IA Eyelid Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Eyelid Carcinoma AJCC v7", "shortest_name_length": 25}
{"curie": "UMLS:C0860029", "names": ["Vaginal Yeast Infection", "yeast vaginal infection", "Vaginal yeast infection", "infection vaginal yeast", "yeast infection vaginal", "vaginal yeast infection", "infections vaginal yeast", "Vaginal Yeast Infections", "Infection, Vaginal Yeast", "Yeast Infection, Vaginal", "Infections, Vaginal Yeast", "Yeast Infections, Vaginal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Yeast Infections", "shortest_name_length": 23}
{"curie": "UMLS:C1266012", "names": ["Micropapillary urothelial carcinoma", "Micropapillary Transitional Cell Carcinoma", "micropapillary transitional cell carcinoma", "Micropapillary transitional cell carcinoma", "Transitional cell carcinoma, micropapillary", "Micropapillary urothelial carcinoma (disorder)", "micropapillary transitional cell carcinoma (diagnosis)", "Micropapillary urothelial carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Micropapillary urothelial carcinoma", "shortest_name_length": 35}
{"curie": "MONDO:0000426", "names": ["AD - Autosomal dominant", "autosomal dominant disease", "disease, autosomal dominant", "Hereditary disorder, dominant", "Dominant hereditary disorder, NOS", "autosomal dominant inherited disorder", "Autosomal dominant hereditary disorder", "autosomal dominant hereditary disorder", "autosomal dominant disease or disorder", "disease or disorder, autosomal dominant", "inherited genetic conditions autosomal dominant", "Autosomal dominant hereditary disorder (disorder)", "Autosomal dominant hereditary disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant disease", "shortest_name_length": 23}
{"curie": "MONDO:0010392", "names": ["PGK deficiency", "PGK Deficiency", "PGK1 deficiency", "Pgk1 deficiency", "PGK1 DEFICIENCY", "PGK1 Deficiency", "PGK1 glycogen storage disease", "Phosphoglycerate Kinase Deficiency", "Phosphoglycerate kinase deficiency", "Phosphoglycerate Kinase 1 Deficiency", "PHOSPHOGLYCERATE KINASE 1 DEFICIENCY", "PHOSPHOGLYCERATE KINASE 1 deficiency", "phosphoglycerate kinase 1 deficiency", "GSD due to phosphoglycerate kinase 1 deficiency", "glycogen storage disease caused by mutation in PGK1", "glycogenosis due to phosphoglycerate kinase 1 deficiency", "phosphoglycerate kinase 1 deficiency, X-linked recessive", "glycogen storage disease due to phosphoglycerate kinase 1 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease due to phosphoglycerate kinase 1 deficiency", "shortest_name_length": 14}
{"curie": "UMLS:C1737224", "names": ["Post procedural swelling"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post procedural swelling", "shortest_name_length": 24}
{"curie": "MONDO:0014738", "names": ["DCUA", "DFNA69", "autosomal dominant deafness 69", "deafness, autosomal dominant 69", "DEAFNESS, AUTOSOMAL DOMINANT 69", "autosomal dominant nonsyndromic deafness 69", "unilateral or asymmetric congenital deafness", "deafness, congenital, unilateral or asymmetric", "DEAFNESS, CONGENITAL, UNILATERAL OR ASYMMETRIC", "KITLG autosomal dominant nonsyndromic deafness", "autosomal dominant nonsyndromic hearing loss 69", "autosomal dominant nonsyndromic deafness type 69", "deafness, autosomal dominant 69, unilateral or asymmetric", "autosomal dominant nonsyndromic deafness caused by mutation in KITLG"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 69", "shortest_name_length": 4}
{"curie": "MONDO:0007760", "names": ["Hyperlipoproteinemia, Type II, and Deafness", "hyperlipoproteinemia, type II, and deafness", "HYPERLIPOPROTEINEMIA, TYPE II, AND DEAFNESS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperlipoproteinemia, type II, and deafness", "shortest_name_length": 43}
{"curie": "MONDO:0035664", "names": ["NMOSD with anti-MOG antibodies", "neuromyelitis optica spectrum disorder with anti-MOG antibodies", "Neuromyelitis optica spectrum disorder with anti-myelin oligodendrocyte glycoprotein antibodies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuromyelitis optica spectrum disorder with anti-MOG antibodies", "shortest_name_length": 30}
{"curie": "MONDO:0035162", "names": ["PROS", "PIK3CA-related overgrowth syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PIK3CA-related overgrowth syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C5556666", "names": ["NHPVA Cervical Adenocarcinoma", "HPV-Independent Cervical Adenocarcinoma", "Human Papillomavirus-Independent Cervical Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Human Papillomavirus-Independent Cervical Adenocarcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0000254", "names": ["cutaneous mycosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous mycosis", "shortest_name_length": 17}
{"curie": "MONDO:0015864", "names": ["Mixed germ cell tumor", "mixed germ cell tumor", "Mixed Germ Cell Tumor", "mixed germ cell cancer", "mixed germ cell tumour", "mixed; germ cell tumor", "Mixed germ cell tumour", "germ cell; tumor, mixed", "tumor; germ cell, mixed", "Mixed Germ Cell Neoplasm", "mixed germ cell neoplasm", "Combined Germ Cell Tumor", "combined germ cell tumor", "[M] Mixed germ cell tumor", "[M] Mixed germ cell tumour", "mixed teratoma and seminoma", "Mixed teratoma and seminoma", "combined germ cell neoplasm", "Combined Germ Cell Neoplasm", "Mixed Teratoma and Seminoma", "Mixed germ cell tumor (disorder)", "mixed germ cell tumor (diagnosis)", "Mixed germ cell tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed germ cell tumor", "shortest_name_length": 21}
{"curie": "UMLS:C0751061", "names": ["Child Craniopharyngioma", "Craniopharyngioma, Child", "Child Craniopharyngiomas", "Craniopharyngiomas, Child"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Craniopharyngioma, Child", "shortest_name_length": 23}
{"curie": "UMLS:C0544617", "names": ["Vasogenic Shock", "neurogenic shock", "Neurogenic Shock", "Neurogenic shock", "shock neurogenic", "Shock, neurogenic", "Neurogenic shock (disorder)", "Neurogenic shock (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neurogenic shock (disorder)", "shortest_name_length": 15}
{"curie": "MONDO:0035670", "names": ["acute disseminated encephalomyelitis without anti-MOG antibodies", "Acute disseminated encephalomyelitis without anti-myelin oligodendrocyte glycoprotein antibodies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute disseminated encephalomyelitis without anti-MOG antibodies", "shortest_name_length": 64}
{"curie": "MONDO:0003881", "names": ["vulvar apocrine adenocarcinoma", "Vulvar Apocrine Adenocarcinoma", "apocrine adenocarcinoma of vulva", "mammalian vulva apocrine adenocarcinoma", "apocrine adenocarcinoma of mammalian vulva", "apocrine adenocarcinoma of vulva (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar apocrine adenocarcinoma", "shortest_name_length": 30}
{"curie": "UMLS:C4527007", "names": ["Stage II Retroperitoneal Sarcoma", "Stage II Retroperitoneal Sarcoma AJCC v8", "Stage II Soft Tissue Retroperitoneal Sarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Retroperitoneal Sarcoma AJCC v8", "shortest_name_length": 32}
{"curie": "UMLS:C2347751", "names": ["Grade I Meningioma", "Adult Grade 1 Meningioma", "adult grade I meningioma", "Adult Grade I Meningioma", "grade I meningioma, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Grade I Meningioma", "shortest_name_length": 18}
{"curie": "UMLS:C1335049", "names": ["Non-Neoplastic Ureter Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Ureter Disorder", "shortest_name_length": 30}
{"curie": "MONDO:0032871", "names": ["HLD19", "hypomyelinating leukodystrophy 19", "LEUKODYSTROPHY, HYPOMYELINATING, 19, TRANSIENT INFANTILE", "leukodystrophy, hypomyelinating, 19, transient infantile"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukodystrophy, hypomyelinating, 19, transient infantile", "shortest_name_length": 5}
{"curie": "MONDO:0023194", "names": ["De Smet-Fabry-Fryns syndrome", "Symbrachydactyly of hands and feet", "Frints De Smet Fabry Fryns syndrome", "frints de Smet Fabry Fryns syndrome", "Symbrachydactyly of the hand and foot"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frints de Smet Fabry Fryns syndrome", "shortest_name_length": 28}
{"curie": "UMLS:C0013504", "names": ["hydatidosis hepatic", "Hepatic Hydatidosis", "hepatic hydatidosis", "Hydatidosis, Hepatic", "Hepatic Hydatid Cyst", "Hydatid Cyst, Hepatic", "Hepatic Hydatid Cysts", "Cyst, Hepatic Hydatid", "echinococcus of liver", "Hepatic Echinococcosis", "hepatic echinococcosis", "Cysts, Hepatic Hydatid", "Hydatid Cysts, Hepatic", "echinococcosis hepatic", "Hepatic echinococciasis", "Echinococcosis of liver", "Echinococcosis, Hepatic", "Echinococcosis of liver, NOS", "ECHINOCOCCAL CYST <S> OF LIVER", "Hepatic Alveolar Echinococcosis", "Alveolar Echinococcosis, Hepatic", "Echinococcosis, Hepatic Alveolar", "echinococcus of liver (diagnosis)", "Echinococcosis of liver (disorder)", "Echinococcosis, unspecified, of liver"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Echinococcosis, Hepatic", "shortest_name_length": 19}
{"curie": "MONDO:0001753", "names": ["Infertility of uterine origin", "female infertility of uterine origin", "Female infertility of uterine origin", "Infertility, female, of uterine origin", "infertility, female, of uterine origin", "Female infertility of uterine origin, NOS", "Female infertility of uterine origin (disorder)", "female infertility of uterine origin (diagnosis)", "infertility; female, associated with disorder or anomaly, uterus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "female infertility of uterine origin", "shortest_name_length": 29}
{"curie": "MONDO:0017290", "names": ["familial intrahepatic cholestasis", "hereditary intrahepatic cholestasis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial intrahepatic cholestasis", "shortest_name_length": 33}
{"curie": "MONDO:0043207", "names": ["EUOS", "Urethral obstruction sequence", "urethral obstruction sequence", "Early urethral obstruction sequence", "early urethral obstruction sequence", "Early urethral obstruction sequence (disorder)", "renal dysplasia or hydronephrosis, oligohydramnios and subsequent lung hypoplasia due to urethral obstruction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urethral obstruction sequence", "shortest_name_length": 4}
{"curie": "MONDO:0004252", "names": ["Small Intestinal L-Cell Glucagon-Like Peptide-Producing NET", "small intestinal L-cell glucagon-like peptide-producing NET", "small intestinal L-cell glucagon-like peptide producing tumor", "small intestine L-cell glucagon-like peptide-producing neuroendocrine tumor", "Small Intestinal L-Cell Glucagon-Like Peptide-Producing Neuroendocrine Tumor", "small intestinal L-cell glucagon-like peptide-producing neuroendocrine tumor", "Small Intestinal L-Cell, Glucagon-Like Peptide-Producing Neuroendocrine Tumor", "small intestinal L-cell, glucagon-like peptide-producing neuroendocrine tumor", "L-cell glucagon-like peptide-producing neuroendocrine tumor of small intestine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small intestinal L-cell glucagon-like peptide producing tumor", "shortest_name_length": 59}
{"curie": "UMLS:C0275959", "names": ["Acute tuberculosis", "tuberculosis acute", "Acute tuberculosis (disorder)", "Acute tuberculosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute tuberculosis", "shortest_name_length": 18}
{"curie": "UMLS:C0861625", "names": ["Tongue Adenoid Cystic Carcinoma", "adenoid cystic carcinoma of tongue", "Adenoid cystic carcinoma of the tongue", "adenoid cystic carcinoma of tongue (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenoid cystic carcinoma of the tongue", "shortest_name_length": 31}
{"curie": "UMLS:C5555544", "names": ["Untreated Diffuse Large B-Cell Lymphoma Activated B-Cell Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Untreated Diffuse Large B-Cell Lymphoma Activated B-Cell Type", "shortest_name_length": 61}
{"curie": "MONDO:0017906", "names": ["amyloidosis cutis dyschromia", "amyloidosis cutis dyschromica", "Amyloidosis cutis dyschromica", "primary localized cutaneous amyloidosis 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyloidosis cutis dyschromia", "shortest_name_length": 28}
{"curie": "MONDO:0002363", "names": ["papilloma", "PAPILLOMA", "Papilloma", "Papillomas", "papillomas", "papillomata", "Papillomata", "Papilloma NOS", "papillomatosis", "Papilloma, NOS", "PAPILLOMA, BENIGN", "papilloma, benign", "Papilloma (disorder)", "non cancerous skin tumor", "papilloma (physical finding)", "papillomatosis NOS (morphologic abnormality)", "papilloma (except papilloma of bladder M-81201) (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papilloma", "shortest_name_length": 9}
{"curie": "UMLS:C5556685", "names": ["Cervical Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Germ Cell Tumor", "shortest_name_length": 24}
{"curie": "UMLS:C0877401", "names": ["Sensorimotor disorder", "Sensorimotor disorder NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sensorimotor disorder", "shortest_name_length": 21}
{"curie": "MONDO:0100312", "names": ["vestibular ataxia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vestibular ataxia", "shortest_name_length": 17}
{"curie": "MONDO:0013609", "names": ["MKS10", "JBTS34", "meckel syndrome 10", "JOUBERT SYNDROME 34", "Joubert syndrome 34", "B9D2 Meckel syndrome", "Meckel syndrome type 10", "Meckel syndrome, type 10", "MECKEL SYNDROME, TYPE 10", "Meckel syndrome type 10 (diagnosis)", "Meckel syndrome caused by mutation in B9D2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meckel syndrome, type 10", "shortest_name_length": 5}
{"curie": "MONDO:0022775", "names": ["cleft lip and palate malrotation cardiopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleft lip and palate malrotation cardiopathy", "shortest_name_length": 44}
{"curie": "UMLS:C5417718", "names": ["SH-HCC", "Steatohepatitic Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Steatohepatitic Hepatocellular Carcinoma", "shortest_name_length": 6}
{"curie": "UMLS:C1334588", "names": ["Malignant Hemangiopericytoma NCI Grade 2", "Malignant Hemangiopericytoma NCI Grade II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Hemangiopericytoma NCI Grade 2", "shortest_name_length": 40}
{"curie": "OMIM:613566", "names": ["HBFQTL6", "FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 6", "HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN, KLF1-RELATED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 7}
{"curie": "MONDO:0003734", "names": ["Adult Central Nervous System Immature Teratoma", "adult central nervous system immature teratoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult central nervous system immature teratoma", "shortest_name_length": 46}
{"curie": "UMLS:C5206775", "names": ["Refractory Kidney Medullary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Kidney Medullary Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0001314", "names": ["cpdd", "CPDD", "PSEUDOGOUT", "pseudogout", "Pseudogout", "pseudo-gout", "pseudo gout", "Pseudo-gout", "Pseudogout, NOS", "Chondrocalcinoses", "CHONDROCALCINOSIS", "Chondrocalcinosis", "chondrocalcinosis", "CPPD (pseudo-gout)", "PSEUDOGOUT SYNDROME", "ARTHRITIS PSEUDOGOUT", "Chondrocalcinosis NOS", "pseudogout (diagnosis)", "Calcium deposits in joints", "Articular chondrocalcinosis", "CHONDROCALCINOSIS, ARTICULAR", "CHONDROCALCINOSIS FAMILIARIS", "Chondrocalcinosis (disorder)", "chondrocalcinosis articularis", "Chondrocalcinosis articularis", "chondrocalcinosis (diagnosis)", "Chondrocalcinosis pyrophosphate", "CPPD CRYSTAL DEPOSITION DISEASE", "Chondrocalcinosis, cause unspecified", "Familial articular chondrocalcinosis", "Calcium pyrophosphate deposition disease", "Calcium Pyrophosphate Deposition Disease", "calcium pyrophosphate deposition disease", "Chondrocalcinosis due to pyrophosphate crystals", "chondrocalcinosis due to pyrophosphate crystals", "CPPD - Calcium pyrophosphate deposition disease", "CPDD - Calcium pyrophosphate deposition disease", "Calcium pyrophosphate arthritis and periarthritis", "Calcium pyrophosphate deposition disease (disorder)", "chondrocalcinosis due to dicalcium phosphate crystals", "Chondrocalcinosis due to dicalcium phosphate crystals", "Chondrocalcinosis due to pyrophosphate crystals (disorder)", "calcium pyrophosphate dihydrate crystal deposition disease", "chondrocalcinosis due to pyrophosphate crystals (diagnosis)", "Chondrocalcinosis due to dicalcium phosphate crystals (disorder)", "chondrocalcinosis due to dicalcium phosphate crystals (diagnosis)", "Chondrocalcinosis, due to pyrophosphate crystals, site unspecified", "Chondrocalcinosis due to dicalcium phosphate crystals with other crystals", "Chondrocalcinosis, due to pyrophosphate crystals, involving unspecified site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chondrocalcinosis", "shortest_name_length": 4}
{"curie": "MONDO:0018613", "names": ["AH amyloidosis", "AH Amyloidosis", "heavy chain amyloidosis", "Heavy chain amyloidosis", "AH amyloidosis (disorder)", "Ig heavy-chain–associated amyloidosis", "immunoglobulin heavy chain amyloidosis", "Amyloidosis derived from immunoglobulin heavy chain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AH amyloidosis", "shortest_name_length": 14}
{"curie": "UMLS:C4289814", "names": ["Cervical Malignant Peripheral Nerve Sheath Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Malignant Peripheral Nerve Sheath Tumor", "shortest_name_length": 48}
{"curie": "MONDO:0002771", "names": ["IPF", "LUNG FIBROSIS", "FIBROSIS LUNG", "fibrosis lung", "Lung fibrosis", "lung fibrosis", "Fibrosis lung", "fibrosis lungs", "cirrhosis lung", "fibrosis; lung", "lung; fibrosis", "lung cirrhosis", "Pneumosclerosis", "Fibrosis of lung", "fibrosis of lung", "Cirrhosis of lung", "Pulmonary fibrosis", "Pulmonary Fibrosis", "FIBROSIS PULMONARY", "PULMONARY FIBROSIS", "pulmonary fibroses", "Fibrosis;pulmonary", "pulmonary fibrosis", "fibrosis pulmonary", "Fibrosis pulmonary", "Pulmonary Fibroses", "fibrosis; pulmonary", "pulmonary; fibrosis", "Fibrosis, Pulmonary", "Fibroses, Pulmonary", "Fibrosis of lung, NOS", "Cirrhosis of lung, NOS", "Fibrosis of lung (disorder)", "pulmonary fibrosis (diagnosis)", "Pulmonary Interstitial Fibrosis", "pulmonary interstitial fibrosis", "Pulmonary interstitial fibrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary fibrosis", "shortest_name_length": 3}
{"curie": "MONDO:0018944", "names": ["GTT", "GTN", "Relapsed GTT", "Recurrent GTT", "recurrent GTT", "GTT, recurrent", "molar pregnancy", "hydatidiform mole", "trophoblastic tumor GTT", "Gestational trophoblastic tumor", "gestational trophoblastic tumor", "Gestational Trophoblastic Tumor", "trophoblastic tumor, gestational", "Gestational trophoblastic tumour", "Persistent trophoblastic disease", "gestational trophoblastic disease", "Gestational trophoblastic neoplasm", "gestational trophoblastic neoplasm", "Gestational Trophoblastic Neoplasm", "gestational trophoblastic neoplasia", "Gestational Trophoblastic Neoplasia", "Gestational trophoblastic tumor NOS", "Gestational Trophoblastic Neoplasms", "Trophoblastic Neoplasm, Gestational", "Neoplasm, Gestational Trophoblastic", "Gestational trophoblastic neoplasia", "Neoplasms, Gestational Trophoblastic", "Trophoblastic Neoplasia, Gestational", "Neoplasia, Gestational Trophoblastic", "Gestational trophoblastic tumour NOS", "Trophoblastic Neoplasms, Gestational", "Relapsed Gestational Trophoblastic Tumor", "Recurrent Gestational Trophoblastic Tumor", "recurrent gestational trophoblastic tumor", "gestational trophoblastic tumor, recurrent", "Relapsed Gestational Trophoblastic Disease", "Recurrent Gestational Trophoblastic Disease", "Relapsed Gestational Trophoblastic Neoplasm", "Persistent gestational trophoblastic disease", "Recurrent Gestational Trophoblastic Neoplasm", "Gestational trophoblastic neoplasia (disorder)", "Gestational trophoblastic neoplasia (diagnosis)", "pregnancy trophoblastic disease gestational neoplasia", "Gestational trophoblastic neoplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gestational trophoblastic neoplasm", "shortest_name_length": 3}
{"curie": "UMLS:C0041665", "names": ["Undersocialized Conduct Disorder, Aggressive Type", "Undersocialized conduct disorder, aggressive type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Undersocialized conduct disorder, aggressive type", "shortest_name_length": 49}
{"curie": "MONDO:0011758", "names": ["MPS1H", "MPSIH", "MPS1-H", "MPS I H", "gargoylism", "Hurler disease", "Hurler syndrome", "Hurler Syndrome", "dysostosis multiplex", "mucopolysaccharidosis Ih", "mucopolysaccharidosis IH", "Hurler-Pfaundler syndrome", "Hurler disease MPS type 1H", "Dysostosis multiplex syndrome", "Mucopolysaccharidosis Type IH", "mucopolysaccharidosis type IH", "mucopolysaccharidosis type 1H", "L-iduronidase deficiency, Hurler type", "Mucopolysaccharidosis type I severe form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hurler syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0018703", "names": ["SGF", "isolated splenogonadal fusion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated splenogonadal fusion", "shortest_name_length": 3}
{"curie": "MONDO:0010475", "names": ["CHTE", "IGSF1 deficiency syndrome", "hypothyroidism Central and testicular enlargement", "central hypothyroidism and testicular enlargement", "Hypothyroidism Central and Testicular Enlargement", "hypothyroidism, central, and testicular enlargement", "HYPOTHYROIDISM, CENTRAL, WITH TESTICULAR ENLARGEMENT", "Immunoglobulin superfamily member 1 deficiency syndrome", "Immunoglobulin Superfamily Member 1 Deficiency Syndrome", "hypothyroidism, central, and testicular enlargement, X-linked recessive", "X-linked central congenital hypothyroidism with late-onset macroorchidism", "X-linked central congenital hypothyroidism with late-onset testicular enlargement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked central congenital hypothyroidism with late-onset testicular enlargement", "shortest_name_length": 4}
{"curie": "EFO:0004795", "names": ["skin sensitivity to sun"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin sensitivity to sun", "shortest_name_length": 23}
{"curie": "MONDO:0005883", "names": ["HZO", "zoster ophthalmic", "Ophthalmic zoster", "ophthalmic zoster", "Zoster ophthalmicus", "zoster ophthalmicus", "ocular herpes zoster", "Ocular herpes zoster", "Ocular Herpes Zoster", "Herpes Zoster, Ocular", "Zoster ocular disease", "Herpes zoster ophthalmic", "ophthalmic herpes zoster", "herpes zoster ophthalmic", "Ophthalmic herpes zoster", "ophthalmicus herpes zoster", "Herpes Zoster Ophthalmicus", "herpes zoster ophthalmicus", "Herpes zoster ophthalmicus", "HERPES ZOSTER OPHTHALMICUS", "herpes zoster, ophthalmicus", "zoster; herpes, eye (etiology)", "herpes; zoster, eye (etiology)", "Herpes zoster ophthalmicus (HZO)", "herpes; eye (h.zoster) (etiology)", "Ophthalmic herpes zoster infection", "Zoster ocular disease, unspecified", "herpes; zoster, eye (manifestation)", "zoster; herpes, eye (manifestation)", "Herpes zoster ophthalmicus (disorder)", "Herpes zoster with ophthalmic complication", "herpes; ophthalmicus (h.zoster) (etiology)", "Herpes zoster with ophthalmic complications", "herpes zoster with ophthalmic complications", "Herpes zoster with ophthalmic complication (disorder)", "herpes zoster with ophthalmic complications (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ophthalmic herpes zoster", "shortest_name_length": 3}
{"curie": "MONDO:0006467", "names": ["Thyroid Gland Squamous Cell Carcinoma", "thyroid gland squamous cell carcinoma", "squamous cell thyroid gland carcinoma", "squamous cell carcinoma of thyroid gland", "squamous cell carcinoma of the thyroid gland", "squamous cell carcinoma of the thyroid gland (diagnosis)", "Thyroid Gland Anaplastic Carcinoma, Squamous Cell Carcinoma Pattern"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid gland squamous cell carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0012304", "names": ["PPR2", "photoparoxysmal response 2", "PHOTOPAROXYSMAL RESPONSE 2", "photoparoxysmal response with or without idiopathic generalized epilepsy", "PHOTOPAROXYSMAL RESPONSE WITH OR WITHOUT IDIOPATHIC GENERALIZED EPILEPSY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "photoparoxysmal response 2", "shortest_name_length": 4}
{"curie": "MONDO:0005036", "names": ["STAD", "Adenocarcinoma", "Gastric adenocarcinoma", "Gastric Adenocarcinoma", "adenocarcinoma stomach", "ADENOCARCINOMA GASTRIC", "gastric adenocarcinoma", "Stomach Adenocarcinoma", "stomach adenocarcinoma", "Adenocarcinoma gastric", "adenocarcinomas gastric", "adenocarcinoma - stomach", "Adenocarcinoma - stomach", "adenocarcinoma of stomach", "Adenocarcinoma of Stomach", "Adenocarcinoma of stomach", "Gastric Adenocarcinoma, NOS", "GASTRIC CANCER ADENOCARCINOMA", "adenocarcinoma of the stomach", "Adenocarcinoma of the stomach", "Adenocarcinoma of the Stomach", "stomach cancer, adenocarcinoma", "stomach, adenocarcinoma of the", "gastric cancer, adenocarcinoma", "Gastric (Stomach) Adenocarcinoma", "gastric (stomach) adenocarcinoma", "Cancer of stomach, adenocarcinoma", "Adenocarcinoma of stomach (disorder)", "adenocarcinoma of stomach (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric adenocarcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0007027", "names": ["NASH", "Fatty Liver Disease", "Nonalcoholic steatohepatitis", "nonalcoholic Steatohepatitis", "Nonalcoholic Steatohepatitis", "nonalcoholic steatohepatitis", "non-alcoholic steatohepatitis", "Non-alcoholic steatohepatitis", "Steatohepatitis, Nonalcoholic", "Steatohepatitis, non-alcoholic", "Nonalcoholic Steatohepatitides", "Steatohepatitides, Nonalcoholic", "NASH - Nonalcoholic Steatohepatitis", "nash - nonalcoholic Steatohepatitis", "Nonalcoholic Steatohepatitis (NASH)", "NASH - Nonalcoholic steatohepatitis", "Nonalcoholic steatohepatitis (NASH)", "Nonalcoholic steatohepatitis (disorder)", "nonalcoholic steatohepatitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-alcoholic steatohepatitis", "shortest_name_length": 4}
{"curie": "MONDO:0008292", "names": ["PPPP", "PPKP2", "type 2 punctate PPK", "punctate palmoplantar keratoderma type 2", "Punctate palmoplantar keratoderma type 2", "keratoderma palmoplantar, punctate type 2", "punctate palmoplantar keratoderma type II", "PALMOPLANTAR KERATODERMA, PUNCTATE TYPE II", "palmoplantar keratoderma, punctate type II", "Keratoderma, Palmoplantar, Punctate Type Ii", "KERATODERMA, PALMOPLANTAR, PUNCTATE TYPE II", "Punctate palmoplantar hyperkeratosis type 2", "punctate palmoplantar hyperkeratosis type 2", "POROKERATOSIS PUNCTATA PALMARIS ET PLANTARIS", "porokeratosis punctata palmaris Et plantaris", "Porokeratosis punctata palmaris et plantaris", "hereditary palmoplantar keratoderma punctate type 2", "Punctate palmoplantar keratoderma type 2 (disorder)", "Punctate palmoplantar keratoderma type 2 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "punctate palmoplantar keratoderma type 2", "shortest_name_length": 4}
{"curie": "MONDO:0020944", "names": ["oculomycosis", "Oculomycosis", "Oculomycoses", "Ocular Mycosis", "Ocular mycosis", "Ocular Mycoses", "ocular mycosis", "Mycosis, Ocular", "Mycoses, Ocular", "EYE INFECT FUNGAL", "FUNGAL EYE INFECT", "Ocular mycosis, NOS", "Eye fungal infection", "Eye infection fungal", "Fungal eye infection", "Fungal Eye Infection", "fungal eye infection", "OCULAR INFECT FUNGAL", "fungal infection eye", "MYCOTIC INFECT OCULAR", "Eye Infection, Fungal", "Fungal eye infections", "Fungal Eye Infections", "Infection, Fungal Eye", "fungal eye infections", "Eye Infections, Fungal", "Infections, Fungal Eye", "Fungal infection of eye", "fungal infection of eye", "Fungal Ocular Infection", "Eye infection fungal NOS", "Infection, Fungal Ocular", "Ocular Mycotic Infection", "Ocular Infection, Fungal", "Fungal Ocular Infections", "Infections, Fungal Ocular", "Ocular Infections, Fungal", "Infection, Ocular Mycotic", "Mycotic Infection, Ocular", "Ocular Mycotic Infections", "Infections, Ocular Mycotic", "Mycotic Infections, Ocular", "Fungal ophthalmic infection", "Fungal infection of eye, NOS", "Fungal infection of eye (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fungal infection of eye", "shortest_name_length": 12}
{"curie": "MONDO:0003246", "names": ["Sclerosing hepatic carcinoma", "sclerosing hepatic carcinoma", "Sclerosing Hepatic Carcinoma", "scirrhous hepatocellular cancer", "Scirrhous Hepatocellular Cancer", "scirrhous hepatocellular carcinoma", "Scirrhous Hepatocellular Carcinoma", "Sclerosing Hepatocellular carcinoma", "Sclerosing Hepatocellular Carcinoma", "sclerosing hepatocellular carcinoma", "Hepatocellular carcinoma, scirrhous", "Hepatocellular carcinoma, scirrhous (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sclerosing hepatic carcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0015364", "names": ["CIP", "hsan", "HSAN", "Neurogenic Acroosteolyses", "Neurogenic Acroosteolysis", "Acroosteolysis, Neurogenic", "Acroosteolyses, Neurogenic", "Hereditary sensory neuropathy", "Congenital Pain Insensitivity", "Sensory neuropathy hereditary", "congenital pain insensitivity", "Hereditary Sensory Neuropathy", "Congenital Sensory Neuropathy", "hereditary sensory neuropathy", "Sensory Neuropathy, Congenital", "Sensory Neuropathy, Hereditary", "familial dysautonomia, type II", "Neuropathy, Congenital Sensory", "Neuropathy, Hereditary Sensory", "hereditary sensory neuropathies", "Congenital Sensory Neuropathies", "neuropathy; hereditary, sensory", "NEUROPATHY, CONGENITAL, SENSORY", "Hereditary Sensory Neuropathies", "sensory; neuropathic, hereditary", "congenital insensitivity to pain", "hereditary; neuropathic, sensory", "Sensory Neuropathies, Congenital", "Sensory Neuropathies, Hereditary", "Neuropathies, Hereditary Sensory", "Congenital Insensitivity to Pain", "Neuropathies, Congenital Sensory", "Hereditary sensory neuropathy, NOS", "Posterior sensory radicular neuropathy", "hereditary sensory autonomic neuropathy", "Hereditary sensory neuropathy (disorder)", "hereditary sensory peripheral neuropathy", "hereditary sensory neuropathy (diagnosis)", "hereditary sensory and autonomic neuropathy", "Hereditary sensory and autonomic neuropathy", "Hereditary Sensory and Autonomic Neuropathies", "Neuropathies, Hereditary Sensory and Autonomic", "HSAN (Hereditary Sensory Autonomic Neuropathy)", "Sensory and Autonomic Neuropathies, Hereditary", "HSANs (Hereditary Sensory Autonomic Neuropathy)", "hereditary sensory and autonomic neuropathy (HSAN)", "HSAN - Hereditary sensory and autonomic neuropathy", "indifference to pain, Congenital, autosomal recessive", "Indifference to Pain, Congenital, Autosomal Recessive", "Hereditary sensory and autonomic neuropathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary sensory and autonomic neuropathy", "shortest_name_length": 3}
{"curie": "MONDO:0011407", "names": ["HCFP2", "MBS3, FORMERLY", "Mobius syndrome 3", "Moebius syndrome 3", "Mobius syndrome 3, formerly", "MOBIUS SYNDROME 3, FORMERLY", "MOEBIUS SYNDROME 3, FORMERLY", "Moebius syndrome 3, formerly", "Facial paresis, hereditary, congenital", "FACIAL PARESIS, HEREDITARY CONGENITAL, 2", "facial paresis, hereditary congenital, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "facial paresis, hereditary congenital, 2", "shortest_name_length": 5}
{"curie": "MONDO:0043224", "names": ["lacunar dementia", "dementia, lacunar", "lacunar Dementias", "Dementias, lacunar", "Binswanger disease", "multifocal dementia", "Binswanger's disease", "Multiinfarct Dementia", "multiinfarct dementia", "dementia multiinfarct", "Multiinfarct dementia", "DEMENTIA MULTI INFARCT", "multi-infarct dementia", "dementia multi-infarct", "Multi-infarct dementia", "Dementia multi-infarct", "Dementia Multi-Infarct", "Multi-Infarct Dementia", "Multi Infarct Dementia", "Dementia Multi Infarct", "Dementia, Multiinfarct", "Multi infarct dementia", "multi infarct dementia", "Multiinfarct Dementias", "dementia multi infarct", "dementia infarct multi", "dementia, Multiinfarct", "Dementias, Multiinfarct", "dementia, multi infarct", "multi-infarct Dementias", "Dementia, Multi-Infarct", "dementia multi-infarcts", "Multi-Infarct Dementias", "dementia; multi-infarct", "DEMENTIA, MULTI-INFARCT", "Dementia Multi-Infarcts", "Dementia, Multi Infarct", "multi-infarct, dementia", "Multi-Infarct, Dementia", "multi-infarct; dementia", "Atherosclerotic dementia", "Multi-Infarcts, Dementia", "ATHEROSCLEROTIC DEMENTIA", "Dementias, Multi-Infarct", "multi-infarcts, dementia", "Dementia (Multi Infarct)", "Dementias, multi-infarct", "Arteriosclerotic dementia", "ARTERIOSCLEROTIC DEMENTIA", "Arteriosclerotic Dementia", "arteriosclerotic dementia", "dementia; arteriosclerotic", "Dementia, Arteriosclerotic", "Psychosis;arteriosclerotic", "arteriosclerotic psychosis", "Arteriosclerotic Dementias", "Multi-infarct dementia, NOS", "psychosis; arteriosclerotic", "Dementias, Arteriosclerotic", "MID - multi-infarct dementia", "MID - Multi-infarct dementia", "Arteriosclerotic dementia NOS", "vascular dementia multi-infarct", "dementia multi-infarct psychosis", "dementia; vascular, multi-infarct", "vascular; dementia, multi-infarct", "Multi-infarct dementia (disorder)", "Multi-infarct dementia (diagnosis)", "Multi-infarct dementia or psychosis", "multi-infarct dementia or psychosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multi-infarct dementia", "shortest_name_length": 16}
{"curie": "UMLS:C1336138", "names": ["Stage IB Lung Cancer", "Stage IB Lung Carcinoma", "Stage IB Carcinoma of Lung", "Stage IB Lung Cancer AJCC v7", "Stage IB Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Lung Cancer AJCC v7", "shortest_name_length": 20}
{"curie": "UMLS:C5667312", "names": ["Metastatic Squamous Cell Carcinoma of the Penis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Squamous Cell Carcinoma of the Penis", "shortest_name_length": 47}
{"curie": "MONDO:0030259", "names": ["PCH15", "pontocerebellar hypoplasia type 15", "pontocerebellar hypoplasia, type 15", "PONTOCEREBELLAR HYPOPLASIA, TYPE 15"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pontocerebellar hypoplasia, type 15", "shortest_name_length": 5}
{"curie": "MONDO:0009115", "names": ["CLD", "Alactasia syndrome", "Congenital alactasia", "congenital alactasia", "Alactasia, Congenital", "ALACTASIA, CONGENITAL", "Alactasia, congenital", "alactasia; congenital", "Lactase deficiency disease", "disaccharide intolerance 2", "Disaccharide intolerance II", "Disaccharide Intolerance II", "disaccharide intolerance II", "DISACCHARIDE INTOLERANCE II", "Congenital lactase deficiency", "Congenital alactasia syndrome", "congenital alactasia syndrome", "congenital lactase deficiency", "Congenital lactose intolerance", "lactase deficiency, congenital", "congenital lactose intolerance", "Lactase Deficiency, Congenital", "LACTASE DEFICIENCY, CONGENITAL", "deficiency; lactase, congenital", "lactase; deficiency, congenital", "Congenital lactose malabsorption", "congenital lactose malabsorption", "lactase deficiency syndrome primary", "primary lactase deficiency syndrome", "CLD - Congenital lactase deficiency", "lactase deficiency syndrome congenital", "Congenital lactase deficiency (disorder)", "primary lactase deficiency syndrome (diagnosis)", "lactase deficiency syndrome congenital (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital lactase deficiency", "shortest_name_length": 3}
{"curie": "UMLS:C4553882", "names": ["Stage IVC Thyroid Gland Anaplastic Carcinoma AJCC v8", "Undifferentiated (Anaplastic) Stage IVC Thyroid Gland Cancer", "Stage IVC Thyroid Gland Undifferentiated (Anaplastic) Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Thyroid Gland Undifferentiated (Anaplastic) Carcinoma AJCC v8", "shortest_name_length": 52}
{"curie": "MONDO:0000375", "names": ["bronchus carcinoma in situ", "bronchus in situ carcinoma", "stage 0 bronchus carcinoma", "Bronchial carcinoma stage 0", "Bronchial carcinoma in situ", "Carcinoma in situ of bronchus", "carcinoma in situ of bronchus", "Carcinoma in situ of bronchus, NOS", "Severe epithelial dysplasia of bronchus", "Carcinoma in situ of bronchus (disorder)", "carcinoma in situ of bronchus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bronchus carcinoma in situ", "shortest_name_length": 26}
{"curie": "MONDO:0016283", "names": ["CELI", "Cervical Leiomyosarcoma", "Cervical leiomyosarcoma", "cervical leiomyosarcoma", "uterine cervix leiomyosarcoma", "Leiomyosarcoma of cervix uteri", "leiomyosarcoma of uterine cervix", "Leiomyosarcoma of the cervix uteri", "leiomyosarcoma of the cervix uteri", "Leiomyosarcoma of cervix uteri (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leiomyosarcoma of the cervix uteri", "shortest_name_length": 4}
{"curie": "UMLS:C5557252", "names": ["Vaso-Occlusive Crisis in Hemoglobin SC Disease", "Vaso-Occlusive Crisis of Hemoglobin SC Disease", "Vaso-Occlusive Crisis in Sickle Cell-Hemoglobin C Disease", "Vaso-Occlusive Crisis of Sickle Cell-Hemoglobin C Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaso-Occlusive Crisis in Sickle Cell-Hemoglobin C Disease", "shortest_name_length": 46}
{"curie": "UMLS:C4087225", "names": ["irAE", "Immune Related Side Effect", "Immune-Related Adverse Event", "Immune-Mediated Adverse Event", "Immune-mediated adverse reaction", "Immune-Mediated Adverse Reaction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immune-mediated adverse reaction", "shortest_name_length": 4}
{"curie": "MONDO:0009140", "names": ["DDSH", "Dyssegmental dwarfism", "Dyssegmental dysplasia", "Lethal Kniest-like syndrome", "Silverman-Handmaker syndrome", "Lethal Kniest-like syndrome (disorder)", "Anisospondylic camptomicromelic dwarfism", "dyssegmental dwarfism Silverman-Handmaker type", "Dyssegmental Dwarfism, Silverman-Handmaker Type", "dyssegmental dysplasia Silverman-Handmaker type", "Silverman-Handmaker type dyssegmental dysplasia", "dyssegmental dwarfism, Silverman-Handmaker type", "Dyssegmental dysplasia Silverman Handmaker type", "DYSSEGMENTAL DWARFISM, SILVERMAN-HANDMAKER TYPE", "Dyssegmental Dysplasia, Silverman-Handmaker Type", "DYSSEGMENTAL DYSPLASIA, SILVERMAN-HANDMAKER TYPE", "dyssegmental dysplasia, Silverman-Handmaker type", "Dyssegmental dysplasia, Silverman-Handmaker type", "Dyssegmental dysplasia - Silverman Handmaker type", "Dyssegmental dysplasia Silverman Handmaker type (disorder)", "dyssegmental dysplasia Silverman-Handmaker type (diagnosis)", "Anisospondylic camptomicromelic dwarfism Silverman-Handmaker type", "Anisospondylic Camptomicromelic dwarfism, Silverman-Handmaker type", "ANISOSPONDYLIC CAMPTOMICROMELIC DWARFISM, SILVERMAN-HANDMAKER TYPE", "Anisospondylic Camptomicromelic Dwarfism, Silverman-Handmaker Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Silverman-Handmaker type dyssegmental dysplasia", "shortest_name_length": 4}
{"curie": "MONDO:0020331", "names": ["ism", "ISM", "Indolent Systemic Mastocytoses", "Indolent systemic mastocytosis", "Indolent Systemic Mastocytosis", "indolent systemic mastocytosis", "Systemic Mastocytosis, Indolent", "Mastocytoses, Indolent Systemic", "Systemic Mastocytoses, Indolent", "Mastocytosis, Indolent Systemic", "Indolent systemic mastocytosis (disorder)", "Indolent systemic mastocytosis (diagnosis)", "Indolent systemic mastocytosis (morphologic abnormality)", "indolent systemic mastocytosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "indolent systemic mastocytosis", "shortest_name_length": 3}
{"curie": "MONDO:0013750", "names": ["ASD8", "ATRIAL SEPTAL DEFECT 8", "atrial septal defect 8", "atrial septal defect type 8", "atrial heart septal defect 8", "atrial septal defect 8 - ASD8", "CITED2 atrial heart septal defect", "atrial heart septal defect type 8", "atrial septal defect 8 - ASD8 (diagnosis)", "atrial heart septal defect caused by mutation in CITED2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial septal defect 8", "shortest_name_length": 4}
{"curie": "MONDO:0004702", "names": ["Cervix Leukoplakia", "cervix leukoplakia", "leukoplakia; cervix", "cervix; leukoplakia", "Cervical leukoplakia", "Cervical Leukoplakia", "Leukoplakia;cervical", "leukoplakia cervical", "cervical leukoplakia", "CERVICAL LEUKOPLAKIA", "Leukoplakia of Cervix", "leukoplakia of cervix", "Leukoplakia of cervix", "Leucoplakia of cervix", "cervix uteri leukoplakia", "Cervix Uteri Leukoplakia", "leukoplakia of the cervix", "Leukoplakia of the Cervix", "Uterine Cervix Leukoplakia", "uterine cervix leukoplakia", "leukoplakia of cervix uteri", "Leukoplakia of Cervix Uteri", "Leukoplakia of cervix uteri", "leukoplakia of cervix (uteri)", "Leukoplakia of Uterine Cervix", "leukoplakia of uterine cervix", "Leukoplakia of cervix (uteri)", "Leukoplakia of the Cervix Uteri", "leukoplakia of the cervix uteri", "Leukoplakia of cervix (disorder)", "leukoplakia of the uterine cervix", "Leukoplakia of the uterine Cervix", "leukoplakia of cervix (diagnosis)", "Leukoplakia of the Uterine Cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine cervix leukoplakia", "shortest_name_length": 18}
{"curie": "MONDO:0003089", "names": ["bile duct mucoepidermoid carcinoma", "Bile Duct Mucoepidermoid Carcinoma", "mucoepidermoidcarcinoma of bile duct", "Mucoepidermoid Carcinoma of Bile Duct", "mucoepidermoid carcinoma of bile duct", "Mucoepidermoid carcinoma of the bile duct", "mucoepidermoid carcinoma of the bile duct", "Mucoepidermoid Carcinoma of the Bile Duct", "Extrahepatic Bile Duct Mucoepidermoid Carcinoma", "extrahepatic bile duct mucoepidermoid carcinoma", "mucoepidermoid carcinoma of the extrahepatic bile duct"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extrahepatic bile duct mucoepidermoid carcinoma", "shortest_name_length": 34}
{"curie": "UMLS:C5235844", "names": ["Advanced Bladder Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Bladder Urothelial Carcinoma", "shortest_name_length": 37}
{"curie": "UMLS:C1333800", "names": ["Gastrointestinal Non-Hodgkin Lymphoma", "Digestive System Non-Hodgkin Lymphoma", "Gastrointestinal Non-Hodgkin's Lymphoma", "Primary Digestive System Non-Hodgkin Lymphoma", "Primary Gastrointestinal Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Digestive System Non-Hodgkin Lymphoma", "shortest_name_length": 37}
{"curie": "UMLS:C2939094", "names": ["Skin sensitization", "Skin sensitisation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin sensitization", "shortest_name_length": 18}
{"curie": "MONDO:0000330", "names": ["Shop typhus", "shop typhus", "urban typhus", "toulon typhus", "murine typhus", "endemic typhus", "Endemic Typhus", "Rat-Flea Typhus", "rat-flea typhus", "fleaborne typhus", "endemic typhus fever", "Endemic Typhus Fever", "Urban Typhus of Malaya", "urban typhus of Malaya", "cat flea rickettsiosis", "endemic flea-borne typhus", "Endemic Flea-Borne Typhus", "Typhus, Endemic Flea-Borne", "Rickettsia felis spotted fever"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endemic typhus", "shortest_name_length": 11}
{"curie": "MONDO:0002175", "names": ["degeneration of macula or posterior pole", "degeneration; eye, macula, posterior pole", "Degeneration of macula and posterior pole", "degeneration of macula and posterior pole", "Degeneration of macula and posterior pole of retina", "degeneration of macula and posterior pole of retina", "degeneration of macula and posterior pole (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "degeneration of macula and posterior pole", "shortest_name_length": 40}
{"curie": "MONDO:0013740", "names": ["RHFCA", "lethal occipital encephalocele-skeletal dysplasia syndrome", "RADIOHUMERAL FUSIONS WITH OTHER SKELETAL AND CRANIOFACIAL ANOMALIES", "radiohumeral fusions with other skeletal and craniofacial anomalies", "craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal occipital encephalocele-skeletal dysplasia syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0007933", "names": ["VMD1", "vitelliform macular dystrophy 1", "macular dystrophy, vitelliform, 1", "MACULAR DYSTROPHY, VITELLIFORM, 1", "MACULAR DYSTROPHY, ATYPICAL VITELLIFORM", "vitelliform macular dystrophy, atypical", "macular dystrophy, atypical vitelliform", "Vitelliform macular dystrophy, atypical", "Macular dystrophy, atypical vitelliform"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitelliform macular dystrophy 1", "shortest_name_length": 4}
{"curie": "MONDO:0014103", "names": ["HH18", "IL17RD hypogonadotropic hypogonadism", "HYPOGONADOTROPIC HYPOGONADISM 18 WITH OR WITHOUT ANOSMIA", "hypogonadotropic hypogonadism 18 with or without anosmia", "hypogonadotropic hypogonadism caused by mutation in IL17RD", "hypogonadotropic hypogonadism 18 with or without anosmia, Autosomal recessive, Autosomal dominant, Digenic dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadotropic hypogonadism 18 with or without anosmia", "shortest_name_length": 4}
{"curie": "MONDO:0004851", "names": ["toxic myocarditis", "Toxic myocarditis", "myocarditis; toxic", "toxic; myocarditis", "Toxic myocarditis (disorder)", "toxic myocarditis (diagnosis)", "Acute toxic disorder of myocardium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "toxic myocarditis", "shortest_name_length": 17}
{"curie": "UMLS:C3203695", "names": ["Noninfectious peritonitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Noninfectious peritonitis", "shortest_name_length": 25}
{"curie": "UMLS:C4525260", "names": ["stage IA intrahepatic bile duct cancer", "Stage IA Intrahepatic Bile Duct Cancer", "stage IA intrahepatic bile duct cancer AJCC v8", "Stage IA Intrahepatic Bile Duct Cancer AJCC v8", "stage IA intrahepatic bile duct carcinoma AJCC v8", "Stage IA Intrahepatic Bile Duct Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Intrahepatic Bile Duct Cancer AJCC v8", "shortest_name_length": 38}
{"curie": "UMLS:C0342782", "names": ["mtDNA depletion syndrome", "dna mitochondrial depletion", "Mitochondrial DNA depletion", "mitochondrial dna depletion", "Mitochondrial DNA depletions", "Depletion of mitochondrial DNA", "Mitochondrial DNA depletion syndrome", "Mitochondrial DNA Depletion Syndromes", "Depletion of mitochondrial deoxyribonucleic acid", "Depletion of mitochondrial deoxyribonucleic acid (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Depletion of mitochondrial DNA", "shortest_name_length": 24}
{"curie": "MONDO:0009712", "names": ["minicore disease", "Minicore Disease", "Minicore disease", "Minicore myopathy", "Minicore Myopathy", "disease; minicore", "MINICORE MYOPATHY", "Multicore Disease", "minicore myopathy", "multicore myopathy", "Multicore Myopathy", "MULTICORE MYOPATHY", "Multiminicore Disease", "Multi-Minicore Disease", "Multiminicore Myopathy", "MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA", "Minicore Myopathy with External Ophthalmoplegia", "minicore myopathy with external ophthalmoplegia", "multicore myopathy with external ophthalmoplegia", "Multicore Myopathy With External Ophthalmoplegia", "Multiminicore Disease With External Ophthalmoplegia", "multiminicore disease with external ophthalmoplegia", "MULTIMINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA", "minicore myopathy, antenatal onset, with arthrogryposis", "MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA (disorder)", "congenital multicore myopathy with external ophthalmoplegia", "Congenital multicore myopathy with external ophthalmoplegia", "multiminicore myopathy multicore myopathy with external ophthalmoplegia", "MULTIMINICORE MYOPATHY MULTICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital multicore myopathy with external ophthalmoplegia", "shortest_name_length": 16}
{"curie": "MONDO:0003846", "names": ["Viral Esophagitis", "viral esophagitis", "Viral esophagitis", "Viral oesophagitis", "Viral esophagitis (disorder)", "Viruses esophagitis (disease)", "Viruses caused esophagitis (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "viral esophagitis", "shortest_name_length": 17}
{"curie": "MONDO:0014514", "names": ["AAT9", "AORTIC ANEURYSM, FAMILIAL THORACIC 9", "aortic aneurysm, familial thoracic 9", "aortic aneurysm, familial thoracic type 9", "AORTIC ANEURYSM, THORACIC, WITH OR WITHOUT AORTIC DISSECTION", "aortic aneurysm, thoracic, with or without aortic dissection", "MFAP5 familial thoracic aortic aneurysm and aortic dissection", "familial thoracic aortic aneurysm and aortic dissection caused by mutation in MFAP5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic aneurysm, familial thoracic 9", "shortest_name_length": 4}
{"curie": "UMLS:C1707439", "names": ["Colorectal Mucinous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Mucinous Adenocarcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0100016", "names": ["DYT-KMT2B", "early-onset generalized dystonia", "early-onset generalized isolated dystonia", "early-onset, generalized dystonia with mild syndromic features", "A generalized isolated dystonia characterized by early-onset, which may be clinically indistinguishable from DYT-TOR1A and may be the most common cause of early-onset generalized dystonia, at least outside the Askenazi Jewish population."], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early-onset generalized dystonia", "shortest_name_length": 9}
{"curie": "MONDO:0005837", "names": ["mandible tumor", "MANDIBLE TUMOR", "mandible cancer", "mandibular tumor", "MANDIBULAR TUMOR", "tumor of mandible", "mandibular cancer", "tumor of lower jaw", "Cancer of mandible", "cancer of mandible", "Mandibular Neoplasm", "mandibular neoplasm", "Neoplasm of mandible", "Mandibular Neoplasms", "neoplasm of mandible", "Neoplasm, Mandibular", "Neoplasms, Mandibular", "malignant mandible neoplasm", "Malignant neoplasm of mandible", "malignant neoplasm of mandible", "Neoplasm of mandible (disorder)", "neoplasm of mandible (diagnosis)", "malignant neoplasm of lower jaw bone", "Malignant neoplasm of lower jaw bone", "malignant neoplasm of lower Jaw bone", "Malignant Neoplasm of Lower Jaw Bone", "malignant neoplasm of inferior maxilla", "Malignant neoplasm of inferior maxilla", "Malignant neoplasm of mandible (disorder)", "malignant neoplasm of mandible (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mandibular cancer", "shortest_name_length": 14}
{"curie": "MONDO:0043346", "names": ["PTGC", "Progressive Transformation of Germinal Centers", "progressive transformation of Germinal centers", "progressive transformation of germinal centers"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive transformation of germinal centers", "shortest_name_length": 4}
{"curie": "MONDO:0012686", "names": ["BPAD", "MAFD6", "BIPOLAR AFFECTIVE DISORDER", "MAJOR affective disorder 6", "bipolar affective disorder", "Major Affective Disorder 6", "MAJOR AFFECTIVE DISORDER 6", "major affective disorder 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "major affective disorder 6", "shortest_name_length": 4}
{"curie": "UMLS:C1384426", "names": ["TONGUE LEUKOPLAKIA HAIRY", "Hairy leucoplakia of tongue", "Hairy leukoplakia of tongue", "Hairy Leukoplakia of Tongue", "Hairy leukoplakia of tongue (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hairy leukoplakia of tongue", "shortest_name_length": 24}
{"curie": "MONDO:0007507", "names": ["BASAN SYNDROME", "Baird syndrome", "Basan syndrome", "BASAN syndrome", "Basan syndrome (disorder)", "absence of fingerprints congenital milia", "absence of dermatoglyphics congenital milia", "Ectodermal dysplasia absent dermatoglyphics", "absence of fingerprints-congenital milia syndrome", "absence of dermatoglyphics-congenital milia syndrome", "ECTODERMAL DYSPLASIA, ABSENT DERMATOGLYPHIC PATTERN, CHANGES IN NAILS, AND SIMIAN CREASE", "ectodermal dysplasia, absent dermatoglyphic pattern, changes in nails, and Simian Crease", "ADERMATOGLYPHIA WITH CONGENITAL FACIAL MILIA AND ACRAL BLISTERS, DIGITAL CONTRACTURES, AND NAIL ABNORMALITIES", "adermatoglyphia with congenital facial milia and acral blisters, digital contractures, and nail abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "absence of fingerprints-congenital milia syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C0280312", "names": ["Floor of Mouth Adenoid Cystic Carcinoma", "adenoid cystic carcinoma of floor of mouth", "Adenoid Cystic Carcinoma of Floor of Mouth", "Adenoid Cystic Carcinoma of the Floor of Mouth", "adenoid cystic carcinoma of floor of mouth (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenoid cystic carcinoma of floor of mouth", "shortest_name_length": 39}
{"curie": "MONDO:0010468", "names": ["ANIB5", "intracranial berry aneurysm 5", "aneurysm, intracranial berry, 5", "Aneurysm, Intracranial Berry, 5", "aneurysm, intracranial BERRY, 5", "ANEURYSM, INTRACRANIAL BERRY, 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aneurysm, intracranial berry, 5", "shortest_name_length": 5}
{"curie": "MONDO:0000128", "names": ["GAN", "Giant Axonal Neuropathy", "giant axonal neuropathy", "Giant axonal neuropathy", "Neuropathy, Giant Axonal", "Axonal Neuropathy, Giant", "Giant Axonal Neuropathy (GAN)", "Neuropathy, Giant Axonal (GAN)", "Axonal Neuropathy, Giant (GAN)", "Giant axonal neuropathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "giant axonal neuropathy", "shortest_name_length": 3}
{"curie": "UMLS:C0278879", "names": ["DUL, childhood", "Burkitt Lymphoma", "pediatric SNC lymphoma", "childhood SNC lymphoma", "SNC lymphoma, childhood", "pediatric Burkitt lymphoma", "childhood Burkitt lymphoma", "Childhood Burkitt Lymphoma", "Pediatric Burkitt's Lymphoma", "Childhood Burkitt's Lymphoma", "childhood small noncleaved cell lymphoma", "pediatric small non-cleaved cell lymphoma", "childhood small non-cleaved cell lymphoma", "Pediatric Small Non-Cleaved Cell Lymphoma", "small noncleaved cell lymphoma, childhood", "Childhood Small Non-Cleaved Cell Lymphoma", "small non-cleaved cell lymphoma, childhood", "lymphoma, small noncleaved cell, childhood", "lymphoma, small non-cleaved cell, childhood", "diffuse undifferentiated lymphoma, childhood", "lymphoma, diffuse undifferentiated, childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Burkitt Lymphoma", "shortest_name_length": 14}
{"curie": "UMLS:C4763796", "names": ["Recurrent Aggressive NK-Cell Leukemia", "Recurrent Aggressive NK-Cell Leukemia/Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Aggressive NK-Cell Leukemia", "shortest_name_length": 37}
{"curie": "MONDO:0012374", "names": ["Brachyphalangy, polydactyly and absent tibiae", "brachyphalangy, polydactyly and absent tibiae", "brachyphalangy, polydactyly, and tibial aplasia/hypoplasia", "BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA", "Brachyphalangy, polydactyly, and tibial aplasia-hypoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachyphalangy, polydactyly, and tibial aplasia/hypoplasia", "shortest_name_length": 45}
{"curie": "UMLS:C5556458", "names": ["Uterine Corpus cPNET", "Uterine Corpus Central Primitive Neuroectodermal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Corpus Central Primitive Neuroectodermal Tumor", "shortest_name_length": 20}
{"curie": "MONDO:0007181", "names": ["axial osteomalacia", "AXIAL OSTEOMALACIA", "Axial osteomalacia", "atypical osteomalacia involving the axial skeleton", "Atypical osteomalacia involving the axial skeleton"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "axial osteomalacia", "shortest_name_length": 18}
{"curie": "UMLS:C0280114", "names": ["stage I adult NHL", "NHL, stage I adult", "Stage I Non-Hodgkin Lymphoma", "stage I adult non-Hodgkin lymphoma", "Stage I Adult Non-Hodgkin Lymphoma", "Stage I Adult Non-Hodgkin's Lymphoma", "adult non-Hodgkin's lymphoma, stage I", "non-Hodgkin's lymphoma, stage I adult", "lymphoma, stage I, adult non-Hodgkin's", "Ann Arbor Stage I Adult Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Adult Non-Hodgkin Lymphoma", "shortest_name_length": 17}
{"curie": "MONDO:0022470", "names": ["aortic dissection lentiginosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic dissection lentiginosis", "shortest_name_length": 30}
{"curie": "UMLS:C2063878", "names": ["ACINAR-ISLET CELL TUMOR, MALIGNANT", "Mucinous Carcinoid Tumor of the Pancreas", "mixed acinar-endocrine carcinoma of pancreas", "Mixed Carcinoid-Adenocarcinoma of the Pancreas", "Mixed Acinar-Endocrine Carcinoma of the Pancreas", "Pancreatic Mixed Acinar-Neuroendocrine Carcinoma", "Mixed Acinar-Neuroendocrine Carcinoma of the Pancreas", "mixed acinar-endocrine carcinoma of pancreas (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed acinar-endocrine carcinoma of pancreas", "shortest_name_length": 34}
{"curie": "MONDO:0005914", "names": ["Picornavirus infection", "Picornavirus Infection", "Picornavirus infections", "Infection, Picornavirus", "Picornavirus Infections", "Infections, Picornavirus", "Picornaviridae Infection", "Picornaviridae infection", "Picornaviridae Infections", "Infection, Picornaviridae", "Infections, Picornaviridae", "infections, Picornaviridae", "Disease due to Picornaviridae", "DISEASES DUE TO PICORNAVIRIDAE", "Disease caused by Picornaviridae", "Picornaviridae infectious disease", "Disease caused by Picornaviridae (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Picornaviridae infectious disease", "shortest_name_length": 22}
{"curie": "UMLS:C5552772", "names": ["STIL", "Serous Tubal Intraepithelial Lesion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Serous Tubal Intraepithelial Lesion", "shortest_name_length": 4}
{"curie": "UMLS:C0267760", "names": ["mesentery; abscess", "Mesenteric abscess", "Mesenteric Abscess", "mesenteric abscess", "Mesenteric abscess (disorder)", "mesenteric abscess (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mesenteric abscess", "shortest_name_length": 18}
{"curie": "UMLS:C0855038", "names": ["Relapsed Alveolar Soft Part Sarcoma", "Alveolar Soft Part Sarcoma Recurrent", "Recurrent Alveolar Soft Part Sarcoma", "Alveolar soft part sarcoma recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alveolar soft part sarcoma recurrent", "shortest_name_length": 35}
{"curie": "MONDO:0012053", "names": ["ANIB2", "intracranial berry aneurysm 2", "Aneurysm, intracranial berry, 2", "ANEURYSM, INTRACRANIAL BERRY, 2", "aneurysm, intracranial berry, 2", "aneurysm, intracranial BERRY, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aneurysm, intracranial berry, 2", "shortest_name_length": 5}
{"curie": "UMLS:C5669689", "names": ["Metastatic Extrahepatic Bile Duct Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Extrahepatic Bile Duct Carcinoma", "shortest_name_length": 43}
{"curie": "UMLS:C0561644", "names": ["Cat bite wound", "Cat bite - wound", "Cat bite - wound (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cat bite - wound", "shortest_name_length": 14}
{"curie": "UMLS:C0280955", "names": ["perioperative/postoperative complications", "Perioperative/Postoperative Complications", "complications, perioperative/postoperative", "complications, postoperative/perioperative"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perioperative/Postoperative Complications", "shortest_name_length": 41}
{"curie": "MONDO:0002328", "names": ["brain hemangioma", "hemangioma of brain", "Intracranial Angioma", "intracranial angioma", "Intracranial hemangioma", "Intracranial Hemangioma", "intracranial hemangioma", "Intracranial haemangioma", "angioma of intracranial structure", "Angioma of intracranial Structure", "Angioma of Intracranial Structure", "intracranial structure hemangioma", "intracranial hemangioma (diagnosis)", "Hemangioma, intracranial structures", "Haemangioma, intracranial structures", "Hemangioma of intracranial structure", "Hemangioma of Intracranial Structure", "hemangioma of intracranial structure", "Haemangioma of intracranial structure", "Angioma of the Intracranial Structure", "hemangioma of intracranial structures", "Hemangioma of intracranial structures", "angioma of the intracranial structure", "Haemangioma of intracranial structures", "hemangioma of the intracranial structure", "Hemangioma of the Intracranial Structure", "Hemangioma of intracranial structure (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intracranial hemangioma", "shortest_name_length": 16}
{"curie": "MONDO:0017765", "names": ["disorder of magnesium transport", "inborn magnesium ion transport disorder", "inborn error of magnesium ion transport", "rare inborn error of magnesium ion transport"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of magnesium transport", "shortest_name_length": 31}
{"curie": "MONDO:0012215", "names": ["MFM3", "LGMD1", "LGMD1A", "LGMD 1A", "MYOTILINOPATHY", "Myotilinopathy", "myotilinopathy", "LGMD1, FORMERLY", "LGMD1A, FORMERLY", "Distal myotilinopathy", "distal myotilinopathy", "spheroid body myopathy", "myofibrillar myopathy 3", "myopathy, myofibrillar, 3", "MYOPATHY, MYOFIBRILLAR, 3", "myofibrillar myopathy type 3", "myopathy, myofibrillar, type 3", "Distal myotilinopathy (disorder)", "Distal myotilinopathy (diagnosis)", "proximal muscular dystrophy type 1A", "Muscular dystrophy, proximal, type 1A", "muscular dystrophy, proximal, type 1A", "muscular dystrophy limb-girdle type 1A", "limb-girdle muscular dystrophy type 1A", "MYOT autosomal dominant distal myopathy", "Muscular Dystrophy, Limb-Girdle, Type1A", "Muscular dystrophy, limb-girdle, type 1A", "muscular dystrophy, limb-girdle, type 1A", "MYOPATHY, MYOFIBRILLAR, MYOTILIN-RELATED", "Myopathy, Myofibrillar, Myotilin-Related", "myopathy, myofibrillar, myotilin-related", "myofibrillar myopathy distal myotilinopathy", "Qualitative or quantitative defects of myotilin", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1, FORMERLY", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1A, FORMERLY", "Limb-girdle muscular dystrophy 1A myotilin myopathy", "MYOT autosomal dominant limb-girdle muscular dystrophy", "Autosomal dominant limb girdle muscular dystrophy type 1A", "Limb-girdle muscular dystrophy due to myotilin deficiency", "autosomal dominant limb-girdle muscular dystrophy type 1A", "Limb girdle muscular dystrophy due to myotilin deficiency", "Autosomal dominant limb-girdle muscular dystrophy type 1A", "limb-girdle muscular dystrophy due to myotilin deficiency", "autosomal dominant distal myopathy caused by mutation in MYOT", "Autosomal dominant limb girdle muscular dystrophy type 1A (disorder)", "autosomal dominant limb-girdle muscular dystrophy caused by mutation in MYOT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myofibrillar myopathy 3", "shortest_name_length": 4}
{"curie": "MONDO:0006257", "names": ["jejunal NET G1", "Jejunal NET G1", "jejunum NET G1", "Jejunal Carcinoid Tumor", "jejunum carcinoid tumor", "jejunal carcinoid tumor", "Carcinoid Tumor of Jejunum", "carcinoid tumor of jejunum", "carcinoid tumor of the jejunum", "Carcinoid Tumor of the Jejunum", "Jejunal Neuroendocrine Tumor G1", "jejunal neuroendocrine tumor G1", "jejunum carcinoid tumor (disease)", "jejunum neuroendocrine neoplasm G1", "grade 1 neuroendocrine neoplasm of jejunum", "jejunum neuroendocrine tumor, well differentiated, low grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "jejunal neuroendocrine tumor G1", "shortest_name_length": 14}
{"curie": "MONDO:0014929", "names": ["RP76", "RETINITIS PIGMENTOSA 76", "retinitis pigmentosa 76", "POMGNT1 retinitis pigmentosa", "retinitis pigmentosa type 76", "retinitis pigmentosa 76; RP76", "retinitis pigmentosa caused by mutation in POMGNT1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 76", "shortest_name_length": 4}
{"curie": "UMLS:C5555674", "names": ["Advanced Digestive System Carcinoid Tumor", "Advanced Digestive System Neuroendocrine Tumor G1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Digestive System Neuroendocrine Tumor G1", "shortest_name_length": 41}
{"curie": "MONDO:0003068", "names": ["Postauricular lymphadenitis", "postauricular lymphadenitis", "Postauricular Lymphadenitis", "mastoid lymph node lymphadenitis (disease)", "lymphadenitis (disease) of mastoid lymph node"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postauricular lymphadenitis", "shortest_name_length": 27}
{"curie": "MONDO:0015404", "names": ["rich", "RICH", "rapidly involuting congenital hemangioma", "Rapidly involuting congenital hemangioma", "Rapidly Involuting Congenital Hemangioma", "Rapidly involuting congenital haemangioma", "RICH - rapidly involuting congenital hemangioma", "RICH - rapidly involuting congenital haemangioma", "Rapidly involuting congenital hemangioma (disorder)", "Rapidly involuting congenital hemangioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rapidly involuting congenital hemangioma", "shortest_name_length": 4}
{"curie": "MONDO:0014421", "names": ["GCCR", "Gcr deficiency", "Grl deficiency", "GCR Deficiency", "GRL DEFICIENCY", "GCR DEFICIENCY", "Gccr deficiency", "GCCR Deficiency", "GCCR DEFICIENCY", "Chrousos Syndrome", "glucocorticoid resistance", "Glucocorticoid Resistance", "glucocorticoid receptor deficiency", "Glucocorticoid Receptor Deficiency", "GLUCOCORTICOID RECEPTOR DEFICIENCY", "Generalized Glucocorticoid Resistance", "GLUCOCORTICOID RESISTANCE, GENERALIZED", "glucocorticoid resistance, generalized", "CORTISOL RESISTANCE FROM GLUCOCORTICOID RECEPTOR DEFECT", "Cortisol Resistance from Glucocorticoid Receptor Defect", "cortisol resistance from glucocorticoid receptor defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glucocorticoid resistance", "shortest_name_length": 4}
{"curie": "UMLS:C2347540", "names": ["adult acute myeloid leukemia with t(8;21)(q22;q22)", "adult acute myeloid leukemia with AML1/ETO translocation", "Adult Acute Myeloid Leukemia with t(8;21)(q22;q22); RUNX1-RUNX1T1", "Adult Acute Myeloid Leukemia with t(8;21)(q22;q22)(AML1(CBFa)/ETO)", "Acute Myeloid Leukemia (AML) with t(8;21); (q22; q22.1); RUNX1-RUNX1T1", "Adult Acute Myeloid Leukemia with t(8;21); (q22; q22.1); RUNX1-RUNX1T1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Acute Myeloid Leukemia with t(8;21); (q22; q22.1); RUNX1-RUNX1T1", "shortest_name_length": 50}
{"curie": "MONDO:0800039", "names": ["MTND5 MELAS syndrome", "MELAS syndrome caused by mutation in MTND5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MELAS syndrome caused by mutation in MTND5", "shortest_name_length": 20}
{"curie": "UMLS:C1332498", "names": ["Benign Extrahepatic Bile Duct Non-Epithelial Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Extrahepatic Bile Duct Non-Epithelial Neoplasm", "shortest_name_length": 53}
{"curie": "MONDO:0005619", "names": ["Typhoid", "typhoid", "Typhoids", "ileotyphus", "Typhoid fever", "TYPHOID FEVER", "Enteric Fever", "typhoid fever", "enteric fever", "Typhoid Fever", "Enteric fever", "Enteric Fevers", "Fever, Enteric", "FEVER, ENTERIC", "Typhoid Fevers", "Fever, Typhoid", "Fevers, Typhoid", "Fevers, Enteric", "Abdominal Typhus", "Typhoid any site", "Typhoid infection", "Typhus, Abdominal", "TYPHUS ABDOMINALIS", "typhoid; infection", "infection; typhoid", "Typhoid fever any site", "typhoidal salmonellosis", "Typhoidal salmonellosis", "Typhoid fever (disorder)", "typhoid fever (diagnosis)", "Salmonella; typhoid fever", "Typhoid infection any site", "Typhoid fever, unspecified", "Salmonella typhi infection", "Salmonella typhi Infection", "Infection, Salmonella typhi", "Salmonella typhi Infections", "infection; Salmonella, typhi", "Infections, Salmonella typhi", "Salmonella; infection, typhi", "Infection by Salmonella typhi", "Infection by Salmonella Typhi"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "typhoid fever", "shortest_name_length": 7}
{"curie": "UMLS:C0521597", "names": ["Ileal hemorrhage", "Hemorrhage ileum", "Ileal Hemorrhage", "HEMORRHAGE ILEUM", "Haemorrhage ileum", "Ileal haemorrhage", "Hemorrhage of ileum", "HEMORRHAGE OF ILEUM", "Haemorrhage of ileum", "Ileal hemorrhage (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ileal hemorrhage", "shortest_name_length": 16}
{"curie": "UMLS:C4744836", "names": ["Recurrent Low Grade Fallopian Tube Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Low Grade Fallopian Tube Serous Adenocarcinoma", "shortest_name_length": 56}
{"curie": "MONDO:0008965", "names": ["HHS", "CHARGE Syndrome", "CHARGE syndrome", "CHARGE SYNDROME", "CHARGE Syndromes", "CHARGE association", "CHARGE Association", "charge association", "CHARGE Associations", "Hall Hittner Syndrome", "Hall-Hittner syndrome", "Hall-Hittner Syndrome", "HALL-HITTNER SYNDROME", "Hall Hittner syndrome", "Familial CHARGE Syndrome", "Familial CHARGE Syndromes", "CHARGE Syndrome, Familial", "CHARGE Syndromes, Familial", "CHARGE syndrome (diagnosis)", "Coloboma, Heart Anomaly, Choanal Atresia, Retardation, Genital and Ear Anomalies", "coloboma, heart anomaly, choanal atresia, retardation, genital and ear anomalies", "CHARGE (coloboma, heart anomaly, choanal atresia, retardation, genital and ear anomalies) syndrome", "CHARGE Association--Coloboma, Heart Anomaly, Choanal Atresia, Retardation, Genital and Ear Anomalies", "Charge association--coloboma, heart anomaly, choanal atresia, retardation, genital and Ear anomalies", "CHARGE ASSOCIATION--COLOBOMA, HEART ANOMALY, CHOANAL ATRESIA, RETARDATION, GENITAL AND EAR ANOMALIES", "Coloboma, congenital heart disease, choanal atresia, growth retardation, genital hypoplasia, ear and hearing anomaly syndrome", "coloboma-heart defects-atresia choanae-retardation of growth and development-genitourinary problems-ear abnormalities syndrome", "Coloboma-heart defects-atresia choanae-retardation of growth and development-genitourinary problems-ear abnormalities syndrome", "Coloboma, heart defects, choanal atresia, retardation of growth and development, genitourinary problems, ear abnormalities syndrome", "coloboma, heart defects, choanal atresia, retardation of Growth and development, genital abnormalities, and Ear anomalies association", "Coloboma, Heart Defects, Choanal Atresia, Retardation of Growth and Development, Genital Abnormalities, and Ear Anomalies Association", "Coloboma, heart malformation, choanal atresia, retardation of growth and development, genital abnormalities, and ear malformations association", "Coloboma, heart defects, choanal atresia, retardation of growth and development, genitourinary problems, ear abnormalities syndrome (disorder)", "coloboma, heart malformation, choanal atresia, retardation of Growth and development, genital abnormalities, and Ear malformations (CHARGE) association", "Coloboma, Heart Malformation, Choanal Atresia, Retardation of Growth and Development, Genital Abnormalities, and Ear Malformations (CHARGE) Association"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CHARGE syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C4528561", "names": ["Stage IV Breast Cancer", "Anatomic Stage IV Breast Cancer AJCC v8", "Anatomic Stage IV Breast Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anatomic Stage IV Breast Cancer AJCC v8", "shortest_name_length": 22}
{"curie": "UMLS:C5239033", "names": ["Thoracic Spine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thoracic Spine Neoplasm", "shortest_name_length": 23}
{"curie": "UMLS:C0452132", "names": ["Congenital Malformation Syndrome due to Known Exogenous Cause", "Congenital malformation syndromes due to known exogenous causes", "congenital malformation syndromes due to known exogenous causes", "Congenital Malformation Syndrome Related to Known Exogenous Cause", "congenital malformation syndromes due to known exogenous causes (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital malformation syndromes due to known exogenous causes", "shortest_name_length": 61}
{"curie": "UMLS:C0686586", "names": ["Acute Leukemia in Remission", "Acute leukemia in remission", "acute leukemia in remission", "Acute leukaemia in remission", "Acute Leukemia (in Remission)", "Acute leukemia (in remission)", "Acute leukemia NOS (in remission)", "Acute leukemia, NOS, in remission", "Acute leukaemia, NOS, in remission", "Acute leukaemia NOS (in remission)", "Acute leukemia in remission (disorder)", "acute leukemia in remission (diagnosis)", "Acute leukemia of unspecified cell type in remission", "Acute leukemia of unspecified cell type, in remission", "Acute leukaemia of unspecified cell type in remission", "Acute leukaemia of unspecified cell type, in remission"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute leukemia in remission", "shortest_name_length": 27}
{"curie": "MONDO:0026404", "names": ["SXI1", "X-inactivation, familial skewed", "X inactivation, familial skewed, 1", "X Inactivation, Familial Skewed, 1", "X-inactivation, familial skewed, 1", "X INACTIVATION, FAMILIAL SKEWED, 1", "X INACTIVATION, FAMILIAL SKEWED, 1 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X inactivation, familial skewed, 1", "shortest_name_length": 4}
{"curie": "UMLS:C2987469", "names": ["psychotic disorder due to substance", "Substance-induced psychotic disorder", "Substance-Induced Psychotic Disorder", "Substance induced psychotic disorder", "Psychotic disorder caused by substance", "psychotic disorder due to substance (diagnosis)", "Psychotic disorder caused by substance (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Substance induced psychotic disorder", "shortest_name_length": 35}
{"curie": "UMLS:C4744841", "names": ["SDH-RCC", "SDH Deficient Renal Cell Carcinoma", "SDH-Deficient Renal Cell Carcinoma", "Succinate Dehydrogenase Renal Cell Carcinoma", "Succinate Dehydrogenase-Deficient Renal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Succinate Dehydrogenase-Deficient Renal Cell Carcinoma", "shortest_name_length": 7}
{"curie": "UMLS:C1262013", "names": ["Recall phenomenon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recall phenomenon", "shortest_name_length": 17}
{"curie": "UMLS:C0854942", "names": ["Stage II Ovarian Choriocarcinoma", "Stage II Ovarian Choriocarcinoma AJCC v6", "Stage II Ovarian Choriocarcinoma AJCC v7", "Ovarian germ cell choriocarcinoma stage II", "Ovarian Germ Cell Choriocarcinoma Stage II", "Stage II Ovarian Germ Cell Choriocarcinoma", "Ovarian Germ Cell Choriocarcinoma, Stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian germ cell choriocarcinoma stage II", "shortest_name_length": 32}
{"curie": "MONDO:0009239", "names": ["HH24", "Isolated FSH deficiency", "isolated FSH deficiency", "FSHB hypogonadotropic hypogonadism", "isolated follicle-stimulating hormone deficiency", "hypogonadotropic hypogonadism 24 without anosmia", "isolated follicle stimulating hormone deficiency", "HYPOGONADOTROPIC HYPOGONADISM 24 WITHOUT ANOSMIA", "Isolated Follicle Stimulating Hormone Deficiency", "Isolated follicle stimulating hormone deficiency", "FOLLICLE-STIMULATING HORMONE DEFICIENCY, ISOLATED", "Follicle-stimulating hormone deficiency, isolated", "follicle-stimulating hormone deficiency, isolated", "Isolated FSH (follicle stimulating hormone) deficiency", "Isolated follicle-stimulating hormone (FSH) deficiency", "isolated follicle-stimulating hormone (FSH) deficiency", "hypogonadotropic hypogonadism caused by mutation in FSHB", "HYPOGONADOTROPIC HYPOGONADISM 24 WITH OR WITHOUT ANOSMIA", "Isolated follicle stimulating hormone deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadotropic hypogonadism 24 without anosmia", "shortest_name_length": 4}
{"curie": "MONDO:0021385", "names": ["extrahepatic bile duct tumor", "Extrahepatic Bile Duct Tumor", "Tumor of extrahepatic bile duct", "Tumor of Extrahepatic Bile Duct", "extrahepatic bile duct neoplasm", "tumor of extrahepatic bile duct", "Extrahepatic Bile Duct Neoplasm", "Tumour of extrahepatic bile duct", "neoplasm of extrahepatic bile duct", "Neoplasm of Extrahepatic Bile Duct", "Neoplasm of extrahepatic bile ducts", "Tumor of the Extrahepatic Bile Duct", "tumor of the extrahepatic bile duct", "neoplasm of the extrahepatic bile duct", "Neoplasm of the Extrahepatic Bile Duct", "extrahepatic bile duct neoplasm (disease)", "Neoplasm of extrahepatic bile ducts (disorder)", "neoplasm of extrahepatic bile duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extrahepatic bile duct neoplasm", "shortest_name_length": 28}
{"curie": "UMLS:C1456853", "names": ["Skin Vascular Tumor", "Vascular Skin Tumor", "Vascular Tumor of Skin", "Vascular Skin Neoplasm", "Vascular tumor of skin", "Skin Vascular Neoplasm", "Vascular tumour of skin", "Cutaneous Vascular Tumor", "Cutaneous vascular tumor", "Vascular Neoplasm of Skin", "Cutaneous vascular tumour", "Vascular neoplasm of skin", "Vascular Tumor of the Skin", "Blood Vessel Tumor of Skin", "Cutaneous Vascular Neoplasm", "Vascular Neoplasm of the Skin", "Blood Vessel Tumor of the Skin", "neoplasm - blood vessels of skin", "Vascular neoplasm of skin (disorder)", "Vascular neoplasm of skin (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vascular neoplasm of skin", "shortest_name_length": 19}
{"curie": "MONDO:0009311", "names": ["GROUPED PIGMENTATION OF THE RETINA", "grouped pigmentation of the macula", "grouped pigmentation of the retina", "GROUPED PIGMENTATION OF THE MACULA", "Grouped Pigmentation of the Macula", "Grouped Pigmentation of Retinal Pigment Epithelium", "GROUPED PIGMENTATION OF RETINAL PIGMENT EPITHELIUM", "grouped pigmentation of retinal pigment epithelium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "grouped pigmentation of the retina", "shortest_name_length": 34}
{"curie": "MONDO:0043247", "names": ["Mallory-Weiss", "esophagus tear", "ESOPHAGUS TEAR", "esophagus tears", "esophagus tearing", "mallory-weiss tear", "MALLORY WEISS TEAR", "Mallory Weiss tear", "mallory weiss tear", "Mallory-Weiss tear", "MALLORY-WEISS TEAR", "Mallory Weiss Tear", "Mallory-Weiss Tear", "mallory weiss tears", "mallory tears weiss", "mallory weiss tearing", "MALLORY WEISS SYNDROME", "Mallory-Weiss Syndrome", "Mallory Weiss syndrome", "mallory weiss syndrome", "Mallory-Weiss syndrome", "mallory-weiss syndrome", "Mallory Weiss Syndrome", "MALLORY-WEISS SYNDROME", "syndrome, Mallory-Weiss", "Syndrome, Mallory-Weiss", "Mallory-Weiss Laceration", "Mallory Weiss Laceration", "Mallory Weiss laceration", "Mallory-Weiss laceration", "laceration, Mallory-Weiss", "Laceration, Mallory-Weiss", "GASTROESOPHAGEAL MUCOSAL TEAR", "Mallory-Weiss tear (disorder)", "Mallory-Weiss tear (diagnosis)", "Mallory-Weiss syndrome (disorder)", "Mallory Weiss syndrome (diagnosis)", "Gastroesophageal laceration syndrome", "Gastro-esophageal laceration syndrome", "gastroesophageal laceration-hemorrhage", "Gastroesophageal Laceration-Hemorrhage", "gastroesophageal laceration hemorrhage", "Gastroesophageal Laceration Hemorrhage", "gastroesophageal laceration-hemorrhages", "laceration-hemorrhage, gastroesophageal", "Laceration-Hemorrhage, Gastroesophageal", "Gastroesophageal Laceration-Hemorrhages", "Laceration-Hemorrhages, Gastroesophageal", "laceration-hemorrhages, gastroesophageal", "Mucosal Lacerations-Gastroesophageal Junction", "mucosal Lacerations gastroesophageal junction", "Mucosal Lacerations Gastroesophageal Junction", "mucosal Lacerations-gastroesophageal junction", "junction, mucosal Lacerations-gastroesophageal", "Lacerations-Gastroesophageal Junction, Mucosal", "Lacerations-gastroesophageal junction, mucosal", "Junction, Mucosal Lacerations-Gastroesophageal", "Mucosal Lacerations-Gastroesophageal Junctions", "mucosal Lacerations-gastroesophageal junctions", "Junctions, Mucosal Lacerations-Gastroesophageal", "junctions, mucosal Lacerations-gastroesophageal", "Lacerations-Gastroesophageal Junctions, Mucosal", "Lacerations-gastroesophageal junctions, mucosal", "Gastroesophageal laceration-hemorrhage syndrome", "gastroesophageal laceration-hemorrhage syndrome", "mucosal lacerations - gastroesophageal junction", "Gastrooesophageal laceration-hemorrhage syndrome", "gastro-esophageal laceration-hemorrhage syndrome", "Gastroesophageal laceration-haemorrhage syndrome", "gastroesophageal; laceration-hemorrhage syndrome", "Gastro-esophageal laceration-hemorrhage syndrome", "syndrome; gastroesophageal laceration-hemorrhage", "Gastrooesophageal laceration-haemorrhage syndrome", "Gastro-oesophageal laceration-haemorrhage syndrome", "GASTROESOPHAGEAL MUCOSAL LACERATION-HEMORRHAGE SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mallory-Weiss syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0004748", "names": ["lip disease", "Lip Disease", "Lip Disorder", "lip; disease", "Disease, Lip", "Lip Diseases", "Lip disorder", "lip disorder", "lips disease", "lip diseases", "disorder lips", "Diseases, Lip", "disorders lip", "lips diseases", "Disease of lip", "disease of lip", "disorders lips", "disorder of lip", "disease of lips", "Disorder of lip", "diseases of lips", "Diseases of lips", "Lip disorder NOS", "Disease of lips, NOS", "diseases of the lips", "DISEASES OF THE LIPS", "lip disease or disorder", "disease (or disorder); lip", "disease or disorder of lip", "Disorder of lip (disorder)", "disorder of lip (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lip disorder", "shortest_name_length": 11}
{"curie": "MONDO:0014346", "names": ["WSN2", "WHITE sponge NEVUS 2", "WHITE SPONGE NEVUS 2", "white sponge nevus 2", "White sponge Nevus type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "white sponge nevus 2", "shortest_name_length": 4}
{"curie": "MONDO:0030914", "names": ["MRD49", "CLABARS", "MRD49, FORMERLY", "Baraitser syndrome", "Baraitser Syndrome", "BARAITSER SYNDROME", "Clark-Baraitser syndrome", "CLARK-BARAITSER SYNDROME", "autosomal dominant mental retardation 49", "mental retardation, autosomal dominant 49", "autosomal dominant intellectual disability 49", "intellectual disability, autosomal dominant 49", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 49, FORMERLY", "mental retardation, tall stature, obesity, macrocephaly and typical facial features", "intellectual disability, tall stature, obesity, macrocephaly and typical facial features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clark-Baraitser syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0003564", "names": ["pulmonary fibrosis localized", "Localised pulmonary fibrosis", "Localized Pulmonary Fibrosis", "Localized pulmonary fibrosis", "localized pulmonary fibrosis", "Localized pulmonary fibrosis (disorder)", "Localized pulmonary fibrosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "localized pulmonary fibrosis", "shortest_name_length": 28}
{"curie": "MONDO:0006840", "names": ["lymphectasia", "Lymphadenovarix", "Lymphangiectasia", "Lymphangiectases", "LYMPHANGIECTASIS", "Lymphangiectasis", "lymphangiectasis", "lymphangiectasia", "lymphangiectasias", "Lymphangiectasis, NOS", "Lymphangiectasia, NOS", "Lymphangiectasia (disorder)", "Lymphangiectasia (diagnosis)", "Lymphangiectasis (morphologic abnormality)", "disorder of lymphatic vessel lymphangiectasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphangiectasis", "shortest_name_length": 12}
{"curie": "MONDO:0008781", "names": ["ALS-dementia complex", "ALS-DEMENTIA COMPLEX", "ALS-dementia Complex", "ALS-Dementia Complex", "juvenile amyotrophic lateral sclerosis with dementia", "AMYOTROPHIC LATERAL SCLEROSIS, JUVENILE, WITH DEMENTIA", "amyotrophic lateral sclerosis, juvenile, with dementia", "Amyotrophic Lateral Sclerosis, Juvenile, with Dementia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile amyotrophic lateral sclerosis with dementia", "shortest_name_length": 20}
{"curie": "UMLS:C5237253", "names": ["Neoantigen-Positive Malignant Solid Tumor", "Neoantigen-Positive Malignant Solid Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoantigen-Positive Malignant Solid Neoplasm", "shortest_name_length": 41}
{"curie": "MONDO:0000751", "names": ["POLYP CERVIX", "Cervix Polyp", "Cervix Tumor", "cervix polyp", "polyp cervix", "cervix tumor", "cervix polyps", "tumor; cervix", "cervix tumors", "polyp; cervix", "cervix; polyp", "Cervical tumor", "cervical polyp", "CERVICAL POLYP", "Cervical Tumor", "Cervical Polyp", "polyp cervical", "Cervical polyp", "Polyp of Cervix", "CERVIX NEOPLASM", "Cervix Neoplasm", "cervical polyps", "Neoplasm cervix", "NEOPLASM CERVIX", "Cervical tumour", "Cervix neoplasm", "polyp of cervix", "tumor of cervix", "cervix neoplasm", "Tumor of cervix", "Tumor of Cervix", "Polyp of cervix", "Tumour of cervix", "Cervix neoplasms", "Cervix Neoplasms", "Neoplasm, Cervix", "cervix neoplasms", "cervical neoplasm", "Neoplasms, Cervix", "Polyp(s);cervical", "Cervical Neoplasm", "Cervical neoplasm", "neoplasm of cervix", "Cervix Uteri Polyp", "Cervical Neoplasms", "cervix uteri polyp", "Cervix Uteri Tumor", "Neoplasm of Cervix", "Tumor of the Cervix", "polyp of the cervix", "Polyp of the Cervix", "Polyp NOS of cervix", "Neoplasms, Cervical", "Uterine Cervix Tumor", "uterine cervix polyp", "Uterine Cervix Polyp", "Polyp of cervix, NOS", "polyp; uterus, cervix", "Cervical neoplasm NOS", "Polyp of cervix uteri", "Tumor of Cervix Uteri", "Polyp of Cervix Uteri", "Cervix Uteri Neoplasm", "uterus; polyp, cervix", "polyp of cervix uteri", "CERVICAL UTERINE POLYP", "Neoplasm of the Cervix", "Cervical uterine polyp", "NEOPLASM UTERINE CERVIX", "Tumor of Uterine Cervix", "polyp of uterine cervix", "Uterine Cervix Neoplasm", "Polyp of Uterine Cervix", "Neoplasm uterine cervix", "Neoplasm of Cervix Uteri", "cervix adenomatous polyp", "Cervix Adenomatous Polyp", "cervical polyp (disease)", "Cervix adenomatous polyp", "polyp of the cervix uteri", "Tumor of the Cervix Uteri", "Polyp of the Cervix Uteri", "Uterine Cervical Neoplasm", "Neoplasm, Uterine Cervical", "Cervical adenomatous polyp", "Neoplasm of Uterine Cervix", "Cervical Neoplasm, Uterine", "Uterine Cervical Neoplasms", "Polyp of cervix (disorder)", "Neoplasm of uterine cervix", "Polyp of cervix adenomatous", "adenomatous polyp of cervix", "Adenomatous Polyp of Cervix", "Adenomatous polyp of cervix", "polyp of the uterine cervix", "Tumor of the Uterine Cervix", "cervical polyps (diagnosis)", "Polyp of the Uterine Cervix", "Neoplasm of the Cervix Uteri", "neoplasm of cervix (diagnosis)", "cervix uteri adenomatous polyp", "Cervix Uteri Adenomatous Polyp", "Neoplasm of the Uterine Cervix", "Adenomatous Polyp of the Cervix", "Other benign neoplasm of uterus", "adenomatous polyp of the cervix", "Uterine Cervix Adenomatous Polyp", "Adenomatous polyp - cervix uteri", "Other benign neoplasms of uterus", "uterine cervix adenomatous polyp", "Adenomatous polyp of cervix uteri", "adenomatous polyp of uterine cervix", "Adenomatous Polyp of Uterine Cervix", "Neoplasm of uterine cervix (disorder)", "Adenomatous Polyp of the Uterine Cervix", "adenomatous polyp of the uterine cervix", "Adenomatous polyp of cervix uteri (disorder)", "Other benign neoplasm of uterus, unspecified", "Other benign neoplasms of uterus, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical polyp", "shortest_name_length": 12}
{"curie": "UMLS:C5237919", "names": ["Non-Neoplastic Musculoskeletal Disorder", "Non-Neoplastic Musculoskeletal System Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Musculoskeletal Disorder", "shortest_name_length": 39}
{"curie": "MONDO:0002523", "names": ["mucinoses", "mucinosis", "Mucinosis", "Mucinoses", "Mucinosis, NOS", "cutaneous mucinosis", "Cutaneous mucinosis", "Mucinosis affecting skin", "mucinosis affecting the skin", "Mucinosis affecting skin (disorder)", "Mucinosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous mucinosis", "shortest_name_length": 9}
{"curie": "UMLS:C1708958", "names": ["Mediastinal T-Lymphoblastic Lymphoma", "Mediastinal T Lymphoblastic Lymphoma", "Mediastinal Precursor T-Lymphoblastic Lymphoma", "Primary Mediastinal Precursor T-Lymphoblastic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mediastinal T Lymphoblastic Lymphoma", "shortest_name_length": 36}
{"curie": "UMLS:C4552014", "names": ["Stage IIA", "Stage IIA Cancer of Testis", "stage IIA cancer of testis", "Stage IIA Testicular Cancer", "stage IIA testicular cancer", "stage IIA cancer of the testis", "Stage IIA Cancer of the Testis", "Stage IIA Testicular Cancer AJCC v6", "stage IIA testicular cancer AJCC v6", "stage IIA testicular cancer AJCC v7", "Stage IIA Testicular Cancer AJCC v7", "Stage IIA Testicular Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Testicular Cancer AJCC v6 and v7", "shortest_name_length": 9}
{"curie": "MONDO:0020490", "names": ["Mosaic trisomy 9", "mosaic trisomy 9", "Trisomy 9 mosaic", "trisomy 9 mosaicism", "Trisomy 9 mosaicism", "Mosaic trisomy type 9", "Mosaic trisomy 9 syndrome", "Mosaic trisomy chromosome 9", "Chromosome 9, trisomy mosaic", "trisomy 9 mosaicism (diagnosis)", "Mosaic trisomy 9 syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mosaic trisomy 9", "shortest_name_length": 16}
{"curie": "UMLS:C0474834", "names": ["Benign Brenner Tumor", "Benign Brenner tumor", "Brenner Tumor, Benign", "Benign Brenner tumour", "Benign Ovarian Brenner Tumor", "benign Brenner tumor of ovary", "Benign Brenner Tumor of Ovary", "Benign Ovarian Brenner Neoplasm", "Benign Brenner Neoplasm of Ovary", "Benign Brenner Tumor of the Ovary", "Benign Brenner Neoplasm of the Ovary", "Benign Ovarian Transitional Cell Tumor", "benign Brenner tumor of ovary (diagnosis)", "Benign Ovarian Transitional Cell Neoplasm", "Benign Brenner tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Brenner Tumor", "shortest_name_length": 20}
{"curie": "UMLS:C0740345", "names": ["Germ cell tumor", "Germ Cell Cancer", "germ cell cancer", "Germ cell cancer", "germ cell cancers", "Germ Cell Cancers", "Cancer, Germ Cell", "cancer cells germ", "Cancers, Germ Cell", "Germ cell cancer NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Germ Cell Cancer", "shortest_name_length": 15}
{"curie": "MONDO:0043529", "names": ["Carcinoid heart disease", "carcinoid heart disease", "Carcinoid Heart Disease", "Carcinoid Heart Diseases", "carcinoid heart diseases", "Heart Disease, Carcinoid", "heart disease, carcinoid", "heart diseases, carcinoid", "Heart Diseases, Carcinoid", "Carcinoid heart disease (disorder)", "heart disease secondary to carcinoid tumor", "heart disease secondary to carcinoid tumor (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoid heart disease", "shortest_name_length": 23}
{"curie": "MONDO:0021345", "names": ["Pharynx Cancer", "pharyngeal cancer", "Cancer of Pharynx", "Pharyngeal cancer", "Pharyngeal Cancer", "pharynx carcinoma", "Pharynx Carcinoma", "PHARYNX, CARCINOMA", "Carcinoma of Pharynx", "PHARYNGEAL CARCINOMA", "pharyngeal carcinoma", "Carcinoma of pharynx", "Pharyngeal carcinoma", "carcinoma of pharynx", "Pharyngeal Carcinoma", "cancer of the pharynx", "Cancer of the Pharynx", "Carcinoma of the Pharynx", "pharyngeal throat cancer", "carcinoma of the pharynx", "Pharyngeal Throat Cancer", "pharyngeal carcinoma cancer", "PHARYNGEAL CANCER, CARCINOMA", "carcinoma of pharynx (diagnosis)", "Malignant epithelial neoplasm of pharynx", "Malignant epithelial neoplasm of pharynx (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma of pharynx", "shortest_name_length": 14}
{"curie": "MONDO:0033631", "names": ["COXPD51", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 51", "combined oxidative phosphorylation deficiency 51"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation deficiency 51", "shortest_name_length": 7}
{"curie": "MONDO:0001391", "names": ["I leprosy", "leprosy; I", "I; leprosy", "Type I leprosy", "Group I leprosy", "indeterminate leprosy", "Indeterminate leprosy", "leprosy; indeterminate", "indeterminate; leprosy", "LEPROSY, INDETERMINATE", "uncharacteristic leprosy", "Uncharacteristic leprosy", "indeterminate leprosy [group I]", "Indeterminate leprosy [group I]", "Indeterminate leprosy (group i)", "Indeterminate leprosy (disorder)", "indeterminate leprosy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "indeterminate leprosy", "shortest_name_length": 9}
{"curie": "MONDO:0033968", "names": ["immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections-lymphopenia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections-lymphopenia syndrome", "shortest_name_length": 99}
{"curie": "MONDO:0008738", "names": ["Total Intestinal Aganglionosis", "total intestinal aganglionosis", "Total intestinal aganglionosis", "AGANGLIONOSIS, TOTAL INTESTINAL", "aganglionosis, total intestinal", "Aganglionosis, total intestinal", "Congenital aganglionic megacolon", "Near-total intestinal aganglionosis", "Total intestinal aganglionosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aganglionosis, total intestinal", "shortest_name_length": 30}
{"curie": "MONDO:0008335", "names": ["Haspeslagh syndrome", "HASPESLAGH SYNDROME", "Haspeslagh Fryns Muelenaere syndrome", "Haspeslagh-Fryns-Muelenaere syndrome", "pterygia mental retardation facial dysmorphism", "pterygia intellectual disability facial dysmorphism", "short stature-craniofacial anomalies-genital hypoplasia syndrome", "Short stature-craniofacial anomalies-genital hypoplasia syndrome", "pterygia, mental retardation and distinctive craniofacial features", "Pterygia, Mental Retardation, And Distinctive Craniofacial Features", "PTERYGIA, MENTAL RETARDATION, AND DISTINCTIVE CRANIOFACIAL FEATURES", "pterygia, mental retardation, and distinctive craniofacial features", "Distinctive craniofacial features with Pterygia and mental retardation", "pterygia, intellectual disability and distinctive craniofacial features", "pterygia, intellectual disability, and distinctive craniofacial features", "Short stature with craniofacial anomalies and genital hypoplasia syndrome", "Mental retardation with pterygia, shortness and distinct facial appearance", "PTERYGIA, IMPAIRED INTELLECTUAL DEVELOPMENT, AND DISTINCTIVE CRANIOFACIAL FEATURES", "Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short stature-craniofacial anomalies-genital hypoplasia syndrome", "shortest_name_length": 19}
{"curie": "MONDO:0018910", "names": ["OCA", "WS2-OA", "Total albinism", "Albinismus totalis", "Albinismus universalis", "Oculocutaneous Albinism", "Oculocutaneous albinism", "oculocutaneous albinism", "albinism oculocutaneous", "Albinism, Oculocutaneous", "albinism, oculocutaneous", "ALBINISM, OCULOCUTANEOUS", "Complete perfect albinism", "Complete universal albinism", "Oculocutaneous albinism, NOS", "OCA - Oculocutaneous albinism", "Albinism, total, oculocutaneous", "Oculocutaneous albinism (disorder)", "oculocutaneous albinism (diagnosis)", "nonsyndromic oculocutaneous albinism", "Oculocutaneous albinism, unspecified", "non-syndromic oculocutaneous albinism", "digenic Waardenburg syndrome/albinism", "ocular albinism with sensorineural deafness", "digenic Waardenburg syndrome/ocular albinism", "autosomal recessive Waardenburg syndrome type 2 with ocular albinism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculocutaneous albinism", "shortest_name_length": 3}
{"curie": "UMLS:C4524750", "names": ["Postneoadjuvant Therapy Stage IVA Gastroesophageal Junction Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postneoadjuvant Therapy Stage IVA Gastroesophageal Junction Adenocarcinoma AJCC v8", "shortest_name_length": 82}
{"curie": "MONDO:0009954", "names": ["Ramon Syndrome", "Ramon syndrome", "RAMON SYNDROME", "gingival fibromatosis combined with cherubism", "Gingival fibromatosis combined with cherubism", "Cherubism-gingival fibromatosis-intellectual disability syndrome", "cherubism-gingival fibromatosis-intellectual disability syndrome", "cherubism-gingival fibromatosis-epilepsy-mental deficiency syndrome", "gingival fibromatosis-hypertrichosis-cherubism-mental retardation-epilepsy syndrome", "cherubism, gingival fibromatosis, epilepsy, mental deficiency, hypertrichosis, and stunted Growth", "CHERUBISM, GINGIVAL FIBROMATOSIS, EPILEPSY, MENTAL DEFICIENCY, HYPERTRICHOSIS, AND STUNTED GROWTH"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ramon syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0024504", "names": ["serotonin-producing PNET", "pancreatic carcinoid tumor", "Pancreatic Carcinoid Tumor", "Carcinoid Tumor of Pancreas", "carcinoid tumor of pancreas", "Carcinoid Neoplasm of Pancreas", "carcinoid neoplasm of pancreas", "Carcinoid Tumor of the Pancreas", "carcinoid tumor of the pancreas", "Carcinoid Neoplasm of the Pancreas", "serotonin-producing pancreatic NET", "carcinoid neoplasm of the pancreas", "pancreatic serotonin producing tumor", "Pancreatic Serotonin Producing Tumor", "Serotonin-Producing Tumor of Pancreas", "serotonin-producing tumor of pancreas", "Pancreatic Serotonin Producing Neoplasm", "pancreatic serotonin producing neoplasm", "Serotonin-Producing Tumor of the Pancreas", "serotonin-producing tumor of the pancreas", "EC Cell, Serotonin Producing Pancreatic NET", "EC cell, serotonin producing pancreatic NET", "Serotonin-Producing Pancreatic Neuroendocrine Tumor", "Pancreatic Serotonin-Producing Neuroendocrine Tumor", "serotonin-producing pancreatic neuroendocrine tumor", "serotonin-producing neuroendocrine tumor of pancreas", "EC Cell, Serotonin Producing Pancreatic Neuroendocrine Tumor", "EC cell, serotonin producing pancreatic neuroendocrine tumor", "enterochromaffin cell serotonin-producing pancreatic neuroendocrine tumor", "Enterochromaffin Cell Serotonin-Producing Pancreatic Neuroendocrine Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "enterochromaffin cell serotonin-producing pancreatic neuroendocrine tumor", "shortest_name_length": 24}
{"curie": "MONDO:0000781", "names": ["cherry allergy", "Prunus avium fruit allergy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cherry allergy", "shortest_name_length": 14}
{"curie": "MONDO:0002262", "names": ["capillary lymphangioma", "cutaneous lymphangioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "capillary lymphangioma", "shortest_name_length": 22}
{"curie": "MONDO:0019128", "names": ["Müllerian aplasia", "mullerian aplasia", "Mullerian aplasia", "Muellerian aplasia", "Müllerian duct failure", "Mullerian duct failure", "Aplasia of Müllerian ducts", "Mullerian aplasia (disorder)", "aplasia of the Mullerian ducts", "Aplasia of the Müllerian ducts", "aplasia of the Müllerian ducts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mullerian aplasia", "shortest_name_length": 17}
{"curie": "MONDO:0004754", "names": ["RECTAL PROLAPSE", "Prolapse;rectal", "rectum prolapse", "rectal prolapse", "prolapse rectum", "Rectal Prolapse", "prolapse rectal", "Rectal prolapse", "Rectal prolapsed", "Rectal Prolapses", "Rectum--Prolapse", "Prolapse, Rectal", "prolapse; rectum", "rectum; prolapse", "RECTUM, PROLAPSE", "Prolapses, Rectal", "Procidentia, rectum", "procidentia, rectum", "RP - Rectal prolapse", "Procidentia of rectum", "Rectal mucosa prolapse", "rectal prolapse (disease)", "Prolapse of rectal mucosa", "Rectal prolapse (disorder)", "rectal prolapse (diagnosis)", "rectal prolapse was observed", "Rectum protrudes through anus", "rectal prolapse (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rectal prolapse", "shortest_name_length": 15}
{"curie": "MONDO:0020154", "names": ["microblepharon-ablephara syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microblepharon-ablephara syndrome", "shortest_name_length": 33}
{"curie": "UMLS:C0155947", "names": ["Dentofacial anomaly", "dentofacial anomaly", "anomaly; dentofacial", "dentofacial; anomaly", "Dentofacial anomaly NOS", "dentofacial anomaly (diagnosis)", "Dentofacial anomaly, unspecified", "Unspecified dentofacial anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dentofacial anomaly", "shortest_name_length": 19}
{"curie": "MONDO:0008054", "names": ["JDM", "JPM", "myositis", "Juvenile DM", "juvenile DM", "myoseptumitis", "Juvenile Myositis", "juvenile myositis", "Myositis, Juvenile", "myoseptum inflammation", "juvenile dermatomyositis", "Juvenile Dermatomyositis", "Juvenile dermatomyositis", "inflammation of myoseptum", "childhood Dermatomyositis", "dermatomyositis; juvenile", "Dermatomyositis, Juvenile", "Childhood dermatomyositis", "childhood dermatomyositis", "Childhood Dermatomyositis", "juvenile; dermatomyositis", "childhood type dermatomyositis", "Childhood type dermatomyositis", "Childhood Type Dermatomyositis", "Dermatomyositis, childhood type", "Dermatomyositis, Childhood Type", "juvenile dermatomyositis (type IV)", "juvenile dermatomyositis (diagnosis)", "Childhood type dermatomyositis (disorder)", "myopathy, familial idiopathic inflammatory"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile dermatomyositis", "shortest_name_length": 3}
{"curie": "MONDO:0017882", "names": ["fever; Omsk", "Omsk; fever", "Omsk Hemorrhagic Fever", "Omsk hemorrhagic fever", "omsk hemorrhagic fever", "Fever, Omsk Hemorrhagic", "hemorrhagic fever; Omsk", "Hemorrhagic Fever, Omsk", "Omsk; hemorrhagic fever", "Omsk haemorrhagic fever", "Hemorrhagic fever, Omsk", "omsk haemorrhagic fever", "OHF - Omsk hemorrhagic fever", "OHF - Omsk haemorrhagic fever", "Omsk hemorrhagic fever (disorder)", "Omsk hemorrhagic fever (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Omsk hemorrhagic fever", "shortest_name_length": 11}
{"curie": "UMLS:C1511323", "names": ["Breast Soft Tissue Tumor", "Breast Soft Tissue Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Soft Tissue Neoplasm", "shortest_name_length": 24}
{"curie": "UMLS:C0686083", "names": ["Small Intestine Cancer Stage 0", "Stage 0 Small Intestinal Cancer", "Cancer in situ of small intestine", "Small intestine carcinoma stage 0", "Small Intestine Carcinoma in situ", "Stage 0 Small Intestine Carcinoma", "carcinoma in situ of small intestine", "Carcinoma in situ of small intestine", "Stage 0 Small Intestinal Cancer AJCC v7", "Carcinoma in situ of small intestine NOS", "Carcinoma in situ of small intestine, NOS", "Carcinoma in situ of small intestine (disorder)", "carcinoma in situ of small intestine (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carcinoma in situ of small intestine", "shortest_name_length": 30}
{"curie": "MONDO:0017574", "names": ["cipo", "CIPO", "chronic intestinal pseudoobstruction", "Chronic intestinal pseudoobstruction", "Intestinal pseudoobstruction, chronic", "chronic intestinal pseudo-obstruction", "Chronic intestinal pseudo-obstruction", "CHRONIC INTESTINAL PSEUDO-OBSTRUCTION", "intestinal pseudo-obstruction, chronic", "Chronic intestinal pseudo-obstruction (disorder)", "chronic intestinal pseudo-obstruction (diagnosis)", "Chronic idiopathic intestinal pseudo-obstruction syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic intestinal pseudoobstruction", "shortest_name_length": 4}
{"curie": "MONDO:0012679", "names": ["OPTB6", "intermediate osteopetrosis", "PLEKHM1 osteopetrosis (disease)", "osteopetrosis autosomal recessive 6", "autosomal recessive osteopetrosis 6", "osteopetrosis, autosomal recessive 6", "Osteopetrosis, Autosomal Recessive 6", "OSTEOPETROSIS, AUTOSOMAL RECESSIVE 6", "autosomal recessive osteopetrosis type 6", "osteopetrosis, autosomal recessive type 6", "autosomal recessive intermediate osteopetrosis", "autosomal recessive osteopetrosis intermediate form", "osteopetrosis autosomal recessive intermediate form", "osteopetrosis (disease) caused by mutation in PLEKHM1", "OSTEOPETROSIS, AUTOSOMAL RECESSIVE, INTERMEDIATE FORM", "osteopetrosis, autosomal recessive, Intermediate form", "Osteopetrosis, Autosomal Recessive, Intermediate Form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive osteopetrosis 6", "shortest_name_length": 5}
{"curie": "MONDO:0011922", "names": ["NI-CINA", "adult idiopathic neutropenia", "Neutropenia, Nonimmune Chronic Idiopathic, Adult", "Nonimmune Chronic Idiopathic Neutropenia of Adults", "nonimmune chronic idiopathic neutropenia of adults", "NONIMMUNE CHRONIC IDIOPATHIC NEUTROPENIA OF ADULTS", "neutropenia, nonimmune chronic idiopathic, of adults", "NEUTROPENIA, NONIMMUNE CHRONIC IDIOPATHIC, OF ADULTS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nonimmune chronic idiopathic neutropenia of adults", "shortest_name_length": 7}
{"curie": "UMLS:C0745178", "names": ["Hypotensive Shock", "HYPOTENSIVE SHOCK"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypotensive Shock", "shortest_name_length": 17}
{"curie": "MONDO:0013134", "names": ["Glc1o", "GLC1O", "NTF4 open-angle glaucoma", "glaucoma 1, open angle, O", "Glaucoma 1, Open Angle, O", "GLAUCOMA 1, OPEN ANGLE, O", "glaucoma 1, open angle, 1O", "Primary Open Angle Glaucoma-1O", "glaucoma 1, open angle, type O", "open-angle glaucoma caused by mutation in NTF4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glaucoma 1, open angle, O", "shortest_name_length": 5}
{"curie": "MONDO:0017182", "names": ["FHI", "HHI", "PHHI", "nesidioblastosis", "Nesidioblastosis", "PHHI Hypoglycemia", "Hypoglycemia, PHHI", "PHHI Hypoglycemias", "Hypoglycemias, PHHI", "Familial hyperinsulinism", "neonatal hyperinsulinism", "Familial Hyperinsulinism", "Neonatal Hyperinsulinism", "familial hyperinsulinism", "Hyperinsulinism, Neonatal", "HYPERINSULINISM, NEONATAL", "Familial Hyperinsulinisms", "HYPERINSULINISM, FAMILIAL", "Neonatal Hyperinsulinisms", "Hyperinsulinism, Familial", "Hyperinsulinisms, Familial", "Hyperinsulinisms, Neonatal", "congenital hyperinsulinism", "Congenital hyperinsulinism", "Congenital Hyperinsulinism", "Hyperinsulinism, Congenital", "Hyperinsulinemia of Infancy", "Congenital Hyperinsulinisms", "HYPERINSULINISM, CONGENITAL", "hyperinsulinemia of infancy", "Hyperinsulinisms, Congenital", "Hyperinsulinemic Hypoglycemia", "hyperinsulinemic hypoglycemia", "Congenital isolated hyperinsulinism", "hereditary hyperinsulinism (disease)", "Infancy Hyperinsulinemia Hypoglycemia", "familial hyperinsulinemic hypoglycemia", "Infancy Hyperinsulinemia Hypoglycemias", "Familial hyperinsulinemic hypoglycemia", "Persistent Hyperinsulinemic Hypoglycemia", "Hyperinsulinemia Hypoglycemia of Infancy", "Familial Hyperinsulinemic Hypoglycemia-1", "Persistent Hyperinsulinemic Hypoglycemias", "HYPERINSULINEMIC HYPOGLYCEMIA, PERSISTENT", "Hyperinsulinemic Hypoglycemia, Persistent", "Hypoglycemia, Persistent Hyperinsulinemic", "Hypoglycemias, Persistent Hyperinsulinemic", "Hypoglycemia, Hyperinsulinemic, of Infancy", "Hyperinsulinemic Hypoglycemias, Persistent", "HYPOGLYCEMIA, HYPERINSULINEMIC, OF INFANCY", "PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY", "Persistent Hyperinsulinemia Hypoglycemia of Infancy", "Persistent Hyperinsulinemic Hypoglycemia of Infancy", "Persistent hyperinsulinemic hypoglycemia of infancy", "Persistent hyperinsulinaemic hypoglycaemia of infancy", "Persistent hyperinsulinemic hypoglycemia of infancy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial hyperinsulinism", "shortest_name_length": 3}
{"curie": "UMLS:C5239027", "names": ["Gastrointestinal Carcinomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal Carcinomatosis", "shortest_name_length": 31}
{"curie": "MONDO:0010243", "names": ["Woods-Black-Norbury Syndrome", "WOODS-BLACK-NORBURY SYNDROME", "Woods Black Norbury syndrome", "Woods-Black-Norbury syndrome", "Neonatal death immune deficiency", "neonatal death immune deficiency", "X-linked immunoneurologic disorder", "IMMUNONEUROLOGIC DISORDER, X-LINKED", "immunoneurologic disorder, X-linked", "Immunoneurologic Disorder, X-Linked", "X-linked immunoneurological disorder", "X-linked immunoneurologic disorder (disorder)", "X-linked immunoneurologic disorder (diagnosis)", "Woods-Black-Norbury syndrome, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked immunoneurologic disorder", "shortest_name_length": 28}
{"curie": "MONDO:0100228", "names": ["LAMA2-related muscular dystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "LAMA2-related muscular dystrophy", "shortest_name_length": 32}
{"curie": "MONDO:0023660", "names": ["HAE6", "ANGIOEDEMA, HEREDITARY, 6", "angioedema, hereditary, 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angioedema, hereditary, 6", "shortest_name_length": 4}
{"curie": "MONDO:0010621", "names": ["child nevus", "CHILD nevus", "Child syndrome", "CHILD Syndrome", "CHILD SYNDROME", "child syndrome", "CHILD syndrome", "syndrome child", "child syndromes", "Child syndrome (disorder)", "ichthyosis, child syndrome", "CHILD syndrome, X-linked dominant", "congenital hemidysplasia with ichthyosiform nevus and limb defects", "Congenital hemidysplasia with ichthyosiform nevus and limbs defects", "congenital hemidysplasia with ichthyosiform nevus and limbs defects", "congenital hemidysplasia with ichthyosiform erythroderma and limb defects", "CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS", "Congenital hemidysplasia with ichthyosiform erythroderma and limb defects", "Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects", "Ichthyosiform Erythroderma, Unilateral, with Ipsilateral Malformations, Especially Absence Deformity Of Limbs", "ichthyosiform erythroderma, unilateral, with ipsilateral malformations, especially absence deformity of limbs", "ICHTHYOSIFORM ERYTHRODERMA, UNILATERAL, WITH IPSILATERAL MALFORMATIONS, ESPECIALLY ABSENCE DEFORMITY OF LIMBS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CHILD syndrome", "shortest_name_length": 11}
{"curie": "UMLS:C1336882", "names": ["Ureteral Transitional Cell Carcinoma with Squamous Differentiation", "Transitional Cell Carcinoma of Ureter with Squamous Differentiation", "Infiltrating Ureter Urothelial Carcinoma with Squamous Differentiation", "Transitional Cell Carcinoma of the Ureter with Squamous Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infiltrating Ureter Urothelial Carcinoma with Squamous Differentiation", "shortest_name_length": 66}
{"curie": "MONDO:0004540", "names": ["Epithelioid MPNST", "epithelioid MPNST", "malignant epithelioid nerve sheath tumor", "Epithelioid malignant nerve sheath tumor", "Epithelioid malignant nerve sheath tumour", "Epithelioid malignant nerve sheath tumor (disorder)", "malignant peripheral nerve sheath tumor epithelioid", "Malignant Epithelioid Peripheral Nerve Sheath Tumor", "Epithelioid Malignant Peripheral Nerve Sheath Tumor", "malignant epithelioid peripheral nerve sheath tumor", "epithelioid malignant peripheral nerve sheath tumor", "Epithelioid malignant peripheral nerve sheath tumor", "Malignant peripheral nerve sheath tumor, epithelioid", "malignant epithelioid nerve sheath tumor (diagnosis)", "Epithelioid malignant peripheral nerve sheath tumour", "Malignant peripheral nerve sheath tumour, epithelioid", "malignant epithelioid tumor of peripheral nerve sheath", "Malignant Epithelioid Tumor of Peripheral Nerve Sheath", "malignant epithelioid peripheral nerve sheath neoplasm", "Malignant Epithelioid Peripheral Nerve Sheath Neoplasm", "Malignant Epithelioid Neoplasm of Peripheral Nerve Sheath", "malignant epithelioid neoplasm of peripheral nerve sheath", "malignant epithelioid tumor of the peripheral nerve sheath", "Malignant Epithelioid Tumor of the Peripheral Nerve Sheath", "malignant epithelioid neoplasm of the peripheral nerve sheath", "malignant epithelioid neoplasm of the peripheral nerve Sheath", "Malignant Epithelioid Neoplasm of the Peripheral Nerve Sheath", "Epithelioid malignant nerve sheath tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epithelioid malignant peripheral nerve sheath tumor", "shortest_name_length": 17}
{"curie": "MONDO:0010437", "names": ["COXPD6", "encephalomyopathy, mitochondrial, X-linked", "ENCEPHALOMYOPATHY, MITOCHONDRIAL, X-LINKED", "Mitochondrial encephalomyopathy due to COXPD6", "mitochondrial encephalomyopathy due to COXPD6", "severe X-linked mitochondrial encephalomyopathy", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6", "Severe X-linked mitochondrial encephalomyopathy", "combined oxidative phosphorylation deficiency 6", "combined oxidative phosphorylation deficiency type 6", "Mitochondrial encephalomyopathy due to COXPD6 deficiency", "Severe X-linked mitochondrial encephalomyopathy (disorder)", "combined oxidative phosphorylation deficiency 6, X-linked recessive", "mitochondrial encephalomyopathy due to combined oxidative phosphorylation defect 6", "Mitochondrial encephalomyopathy due to combined oxidative phosphorylation defect 6", "Mitochondrial encephalomyopathy due to combined oxidative phosphorylation deficiency 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe X-linked mitochondrial encephalomyopathy", "shortest_name_length": 6}
{"curie": "MONDO:0018245", "names": ["Del(2)(p21) without cystinuria", "2p21 microdeletion syndrome without cystinuria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "2p21 microdeletion syndrome without cystinuria", "shortest_name_length": 30}
{"curie": "MONDO:0007938", "names": ["SRXY4", "46,XY sex reversal 4", "46,XY SEX REVERSAL 4", "46,XY Sex Reversal 4", "46,XY SEX reversal 4", "46,XY Sex reversal type 4", "46XY sex reversal 4, Isolated cases", "chromosome 9p24.3 deletion syndrome", "CHROMOSOME 9p24.3 DELETION SYNDROME", "Chromosome 9p24.3 Deletion Syndrome", "chromosome 9P24.3 deletion syndrome", "46,XY gonadal dysgenesis, partial or complete, with 9p24.3 deletion", "46,XY GONADAL DYSGENESIS, PARTIAL OR COMPLETE, WITH 9p24.3 DELETION", "46,XY gonadal dysgenesis, partial or complete, with 9P24.3 deletion", "46,Xy Gonadal Dysgenesis, Complete Or Partial, With 9p24.3 Deletion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XY sex reversal 4", "shortest_name_length": 5}
{"curie": "UMLS:C1697984", "names": ["Urostomy obstruction", "Urostomy Obstruction", "Urostomy obstruction (diagnosis)", "postprocedural complications urostomy obstruction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urostomy Obstruction", "shortest_name_length": 20}
{"curie": "MONDO:0012068", "names": ["Brachial Palsy, Familial Congenital", "brachial palsy, familial congenital", "BRACHIAL PALSY, FAMILIAL CONGENITAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachial palsy, familial congenital", "shortest_name_length": 35}
{"curie": "MONDO:0014336", "names": ["MRD23", "autosomal dominant mental retardation 23", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 23", "mental retardation, autosomal dominant 23", "autosomal dominant intellectual disability 23", "intellectual disability, autosomal dominant 23", "mental retardation, autosomal dominant type 23", "intellectual disability, autosomal dominant type 23", "autosomal dominant intellectual developmental disorder 23", "intellectual developmental disorder, autosomal dominant 23", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 23", "autosomal dominant non-syndromic intellectual disability 23", "intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency", "shortest_name_length": 5}
{"curie": "MONDO:0001055", "names": ["web eye", "Web eye", "conjunctival pterygium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "conjunctival pterygium", "shortest_name_length": 7}
{"curie": "MONDO:0009854", "names": ["peroneus tertius muscle, absence of", "PERONEUS TERTIUS MUSCLE, ABSENCE OF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroneus tertius muscle, absence of", "shortest_name_length": 35}
{"curie": "UMLS:C1541270", "names": ["Stage IV Marginal Zone Lymphoma", "stage IV marginal zone lymphoma", "Marginal zone lymphoma stage IV", "stage IV marginal zone B-cell lymphoma", "Stage IV Marginal Zone B-Cell Lymphoma", "Ann Arbor Stage IV Marginal Zone Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Marginal zone lymphoma stage IV", "shortest_name_length": 31}
{"curie": "MONDO:0022555", "names": ["Beardwell syndrome", "familial ankylosing vertebral hyperostosis with tylosis", "Familial ankylosing vertebral hyperostosis with tylosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Beardwell syndrome", "shortest_name_length": 18}
{"curie": "UMLS:C1515295", "names": ["Testicular Seminoma with Syncytiotrophoblastic Cells"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular Seminoma with Syncytiotrophoblastic Cells", "shortest_name_length": 52}
{"curie": "UMLS:C0495025", "names": ["Biomechanical Lesion", "biomechanical; lesion", "Biomechanical lesions", "lesion; biomechanical", "Unspecified biomechanical lesion", "Biomechanical lesion, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Biomechanical lesion, unspecified", "shortest_name_length": 20}
{"curie": "MONDO:0006555", "names": ["Granulomatous Dermatitis", "granulomatous dermatitis", "DERMATITIS GRANULOMATOUS", "Granulomatous dermatitis", "Granulomatous dermatitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "granulomatous dermatitis", "shortest_name_length": 24}
{"curie": "MONDO:0010869", "names": ["Motor Neuron Disease with Dementia and Ophthalmoplegia", "MOTOR NEURON DISEASE WITH DEMENTIA AND OPHTHALMOPLEGIA", "motor neuron disease with dementia and ophthalmoplegia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "motor neuron disease with dementia and ophthalmoplegia", "shortest_name_length": 54}
{"curie": "UMLS:C1334417", "names": ["Low Grade Mucoepidermoid Breast Carcinoma", "Low Grade Breast Mucoepidermoid Carcinoma", "Low-Grade Mucoepidermoid Carcinoma of Breast", "Low-Grade Mucoepidermoid Carcinoma of the Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Grade Breast Mucoepidermoid Carcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0002850", "names": ["CNS Rhabdomyosarcoma", "CNS rhabdomyosarcoma", "rhabdomyosarcoma of CNS", "Rhabdomyosarcoma of CNS", "Rhabdomyosarcoma of the CNS", "rhabdomyosarcoma of the CNS", "central nervous system rhabdomyosarcoma", "Central Nervous System Rhabdomyosarcoma", "rhabdomyosarcoma of central nervous system", "Rhabdomyosarcoma of Central Nervous System", "Rhabdomyosarcoma of the Central Nervous System", "rhabdomyosarcoma of the central nervous system", "central nervous system rhabdomyosarcoma (disease)", "rhabdomyosarcoma (disease) of central nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system rhabdomyosarcoma", "shortest_name_length": 20}
{"curie": "UMLS:C0855242", "names": ["Disturbance in sexual arousal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disturbance in sexual arousal", "shortest_name_length": 29}
{"curie": "MONDO:0003494", "names": ["Ovarian Squamous Cell Cancer", "ovarian squamous cell cancer", "ovary squamous cell carcinoma", "ovarian squamous cell neoplasm", "Ovarian Squamous Cell Carcinoma", "ovarian squamous cell carcinoma", "squamous cell carcinoma of ovary", "squamous cell carcinoma of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian squamous cell carcinoma", "shortest_name_length": 28}
{"curie": "UMLS:C4527335", "names": ["Refractory Intravascular B-Cell Lymphoma", "Refractory Intravascular Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Intravascular Large B-Cell Lymphoma", "shortest_name_length": 40}
{"curie": "MONDO:0100447", "names": ["ACHM7", "achromatopsia 7", "ATF6 retinopathy", "ATF6 achromatopsia", "achromatopsia type 7", "ATF6-related retinopathy", "achromatopsia caused by mutation in ATF6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ATF6-related retinopathy", "shortest_name_length": 5}
{"curie": "MONDO:0023106", "names": ["osteorhabdotosis", "Fairbank disease", "Voorhoeve syndrome", "Voorhoeve dyschondroplasia", "dysplasia epiphysealis multiplex", "Dysplasia epiphysealis multiplex", "Epiphyseal dysplasia Fairbank type", "epiphyseal dysplasia Fairbank type", "epiphyseal dysplasia, ribbing type", "Epiphyseal Dysplasia, Fairbank Type", "EPIPHYSEAL DYSPLASIA, FAIRBANK TYPE", "epiphyseal dysplasia, Fairbank type", "Fairbank multiple epiphyseal dysplasia", "hyperostosis generalisata with striations", "osteopathia striata with cranial sclerosis", "cranial sclerosis with striated bone disease", "cranial sclerosis-osteopathia striata macrocephaly syndrome", "osteopathia striata-deafness-cranial osteopetrosis syndrome", "osteopathia striata-macrocephaly-cranial sclerosis syndrome", "megalencephaly-cranial sclerosis-osteopathia striata syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fairbank disease", "shortest_name_length": 16}
{"curie": "MONDO:0004208", "names": ["superior vena cava leiomyosarcoma", "anterior vena cava leiomyosarcoma", "Superior Vena Cava Leiomyosarcoma", "leiomyosarcoma of anterior vena cava", "Leiomyosarcoma of Superior Vena Cava", "leiomyosarcoma of Superior vena cava", "leiomyosarcoma of the Superior vena cava", "leiomyosarcoma of the Superior Vena Cava", "Leiomyosarcoma of the Superior Vena Cava"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "superior vena cava leiomyosarcoma", "shortest_name_length": 33}
{"curie": "MONDO:0001990", "names": ["heart MPNST", "Heart MPNST", "Cardiac MPNST", "MPNST of heart", "MPNST of Heart", "MPNST of the Heart", "MPNST of the heart", "Malignant Heart Schwannoma", "malignant heart schwannoma", "malignant heart neurilemmoma", "Malignant Heart Neurilemmoma", "Malignant Cardiac Schwannoma", "malignant Cardiac schwannoma", "CARDIAC SCHWANNOMA, MALIGNANT", "Malignant Schwannoma of Heart", "malignant schwannoma of heart", "CARDIAC schwannoma, malignant", "malignant Cardiac neurilemmoma", "Malignant Cardiac Neurilemmoma", "malignant neurilemmoma of heart", "Malignant Neurilemmoma of Heart", "Malignant Schwannoma of the Heart", "malignant schwannoma of the heart", "Malignant Neurilemmoma of the Heart", "malignant neurilemmoma of the heart", "Heart Malignant Peripheral Nerve Sheath Tumor", "heart malignant peripheral nerve sheath tumor", "Malignant Heart Peripheral Nerve Sheath Tumor", "malignant heart peripheral nerve sheath tumor", "Cardiac malignant peripheral nerve sheath tumor", "Cardiac Malignant Peripheral Nerve Sheath Tumor", "malignant Cardiac peripheral nerve sheath tumor", "Malignant Cardiac Peripheral Nerve Sheath Tumor", "Malignant Heart Peripheral Nerve Sheath Neoplasm", "malignant peripheral nerve sheath tumor of heart", "Malignant Peripheral Nerve Sheath Tumor of Heart", "malignant heart peripheral nerve sheath neoplasm", "malignant cardiac peripheral nerve sheath neoplasm", "malignant Cardiac peripheral nerve sheath neoplasm", "Malignant Cardiac Peripheral Nerve Sheath Neoplasm", "Malignant Peripheral Nerve Sheath Neoplasm of Heart", "malignant peripheral nerve sheath neoplasm of heart", "Malignant Peripheral Nerve Sheath Tumor of the Heart", "malignant peripheral nerve sheath tumor of the heart", "Malignant Peripheral Nerve Sheath Neoplasm of the Heart", "malignant peripheral nerve sheath neoplasm of the heart"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant cardiac peripheral nerve sheath neoplasm", "shortest_name_length": 11}
{"curie": "UMLS:C0398609", "names": ["AHB", "Acquired hemophilia B", "Acquired F9 deficiency", "Hemophilia B, acquired", "Acquired Factor IX Deficiency", "Acquired factor IX deficiency", "Acquired factor IX deficiency disease", "Acquired factor IX deficiency disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired factor IX deficiency disease", "shortest_name_length": 3}
{"curie": "UMLS:C4521812", "names": ["Stage IIIA Appendix Cancer", "Stage IIIA Appendix Carcinoma AJCC v8", "Stage IIIA Appendiceal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Appendix Carcinoma AJCC v8", "shortest_name_length": 26}
{"curie": "UMLS:C5420761", "names": ["Conjunctival Pseudoglandular Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conjunctival Pseudoglandular Hyperplasia", "shortest_name_length": 40}
{"curie": "UMLS:C4725876", "names": ["Resectable Neuroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Neuroblastoma", "shortest_name_length": 24}
{"curie": "MONDO:0009695", "names": ["MYELOPROLIFERATIVE DISEASE, AUTOSOMAL RECESSIVE", "Myeloproliferative Disease, Autosomal Recessive", "myeloproliferative disease, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myeloproliferative disease, autosomal recessive", "shortest_name_length": 47}
{"curie": "UMLS:C0333879", "names": ["Severe Columnar Cell Atypia", "Severe columnar cell atypia", "Severe columnar cell atypia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Severe columnar cell atypia", "shortest_name_length": 27}
{"curie": "UMLS:C3831088", "names": ["Class 1 Uveal Melanoma", "Uveal Class 1 Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uveal Class 1 Melanoma", "shortest_name_length": 22}
{"curie": "MONDO:0010538", "names": ["Mononen type brachydactyly", "brachydactyly Mononen type", "brachydactyly, Mononen type", "BRACHYDACTYLY, MONONEN TYPE", "Mononen-Karnes-Senac syndrome", "Mononen Karnes Senac syndrome", "skeletal dysplasia brachydactyly", "short and abducted thumbs and great toes", "thumbs and great toes short and abducted", "Skeletal dysplasia-brachydactyly syndrome", "thumbs and great toes, short and abducted", "skeletal dysplasia brachydactyly syndrome", "Skeletal dysplasia brachydactyly syndrome", "skeletal dysplasia-brachydactyly syndrome", "THUMBS AND GREAT TOES, SHORT AND ABDUCTED", "x-linked skeletal dysplasia brachydactyly syndrome", "Skeletal dysplasia brachydactyly syndrome (disorder)", "skeletal dysplasia brachydactyly syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mononen-Karnes-Senac syndrome", "shortest_name_length": 26}
{"curie": "MONDO:0014082", "names": ["IMD56", "IMMUNODEFICIENCY 56", "immunodeficiency 56", "IL21R immunodeficiency", "IL21R IMMUNODEFICIENCY", "combined immunodeficiency due to IL21R deficiency", "cryptosporidiosis-chronic cholangitis-liver disease syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cryptosporidiosis-chronic cholangitis-liver disease syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0000499", "names": ["AION", "NAION", "non-arteritic aion", "Nonarteritic Anterior Ischemic Optic Neuropathy", "Nonarteritic anterior ischemic optic neuropathy", "nonarteritic anterior ischemic optic neuropathy", "non-arteritic anterior ischemic optic neuropathy", "Nonarteritic anterior ischaemic optic neuropathy", "nonarteritic anterior ischaemic optic neuropathy", "non-arteritic anterior ischaemic optic neuropathy", "Nonarteritic anterior ischemic optic neuropathy (NAION)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-arteritic anterior ischemic optic neuropathy", "shortest_name_length": 4}
{"curie": "MONDO:0014099", "names": ["NPHS8", "nephrotic syndrome type 8", "ARHGDIA nephrotic syndrome", "NEPHROTIC SYNDROME, TYPE 8", "nephrotic syndrome, type 8", "nephrotic syndrome caused by mutation in ARHGDIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrotic syndrome, type 8", "shortest_name_length": 5}
{"curie": "MONDO:0001025", "names": ["seminal vesicle chronic gonorrhea", "Gonorrhea of seminal vesicle, chronic", "Chronic gonococcal seminal vesiculitis", "chronic gonococcal seminal vesiculitis", "Gonococcal seminal vesiculitis, chronic", "gonococcal seminal vesiculitis, chronic", "Chronic gonococcal seminal vesiculitis (disorder)", "chronic gonococcal seminal vesiculitis (diagnosis)", "Gonococcal seminal vesiculitis specified as chronic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "seminal vesicle chronic gonorrhea", "shortest_name_length": 33}
{"curie": "MONDO:0006874", "names": ["Cholestatic icterus", "Mechanical jaundice", "Mechanical Jaundice", "cholestatic icterus", "JAUNDICE CHOLESTATIC", "Jaundice cholestatic", "jaundice obstructive", "Obstructive Jaundice", "Jaundice;obstructive", "Cholestatic jaundice", "Cholestatic Jaundice", "obstructive jaundice", "cholestatic jaundice", "CHOLESTATIC JAUNDICE", "JAUNDICE OBSTRUCTIVE", "Obstructive jaundice", "Jaundice, Mechanical", "jaundice cholestatic", "obstructive; jaundice", "jaundice; obstructive", "Jaundice, Cholestatic", "Jaundice, Obstructive", "JAUNDICE, CHOLESTATIC", "Jaundice, obstructive", "JAUNDICE, OBSTRUCTIVE", "regurgitation; jaundice", "jaundice; regurgitation", "JAUNDICE, REGURGITATION", "Cholestatic jaundice, NOS", "cholestatic jaundice syndrome", "Cholestatic jaundice syndrome", "Obstructive hyperbilirubinemia", "obstructive hyperbilirubinemia", "Obstructive hyperbilirubinaemia", "Cholestatic jaundice syndrome, NOS", "Cholestatic jaundice syndrome (disorder)", "Obstructive hyperbilirubinemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "obstructive jaundice", "shortest_name_length": 19}
{"curie": "MONDO:0020690", "names": ["glioblastoma", "Glioblastoma", "adult glioblastoma", "Adult Glioblastoma", "grade IV adult astrocytoma", "astrocytoma, grade IV adult", "adult glioblastoma multiforme", "glioblastoma multiforme adult", "Adult Glioblastoma Multiforme", "glioblastoma multiforme, adult", "grade IV adult astrocytic tumor", "Brain tumor, adult: Glioblastoma", "grade IV adult astrocytic neoplasm", "CNS tumor, adult grade IV astrocytoma", "CNS tumor, grade IV adult astrocytoma", "brain tumor, adult grade IV astrocytoma", "CNS tumor, adult glioblastoma multiforme", "adult CNS tumor, glioblastoma multiforme", "brain tumor, adult glioblastoma multiforme", "adult brain tumor, glioblastoma multiforme", "central nervous system tumor, astrocytoma, grade IV adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult glioblastoma", "shortest_name_length": 12}
{"curie": "MONDO:0013162", "names": ["MDDGC2", "LGMD2N", "LGMDR14", "LGMD type 2N", "LGMD-POMT2 related", "POMT2-related LGMD R14", "limb-girdle muscular dystrophy type 2N", "Limb-girdle muscular dystrophy type 2N", "muscular dystrophy, limb-girdle, type 2N", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2N", "POMT2-related limb-girdle muscular dystrophy R14", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 14", "POMT2 autosomal recessive limb-girdle muscular dystrophy", "Autosomal recessive limb girdle muscular dystrophy type 2N", "Autosomal recessive limb-girdle muscular dystrophy type 2N", "autosomal recessive limb-girdle muscular dystrophy type 2N", "muscular dystrophy-dystroglycanopathy (limb-girdle) type C 2", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 2", "muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 2", "muscular dystrophy-dystroglycanopathy limb-girdle POMT2-related", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, POMT2-RELATED", "muscular dystrophy-dystroglycanopathy, limb-girdle, Pomt2-related", "Autosomal recessive limb girdle muscular dystrophy type 2N (disorder)", "autosomal recessive limb-girdle muscular dystrophy caused by mutation in POMT2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive limb-girdle muscular dystrophy type 2N", "shortest_name_length": 6}
{"curie": "UMLS:C0948198", "names": ["Acholia", "acholia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acholia", "shortest_name_length": 7}
{"curie": "MONDO:0007765", "names": ["HCIN", "hyperostosis cranalis interna", "Hyperostosis cranialis interna", "HYPEROSTOSIS CRANIALIS INTERNA", "hyperostosis cranialis interna", "Hyperostosis Cranialis Interna", "Overgrowth of the inside of the skull", "Thick inner surface of the skull bones", "hyperostosis cranialis interna (disease)", "Hyperostosis cranialis interna (disorder)", "Thick internal surface of the cranial bones", "Overgrowth of the inner surface of the skull bones", "Enlargement of the inner surface of the skull bones", "Excessive growth of inner surface of the skull bones", "Hyperostosis of the internal surface of the cranial bone", "Hypertrophy of the internal surface of the cranial bones", "Hyperostosis of the internal surface of the cranial bones", "Increased ossification of the internal surface of the cranial bones"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperostosis cranialis interna", "shortest_name_length": 4}
{"curie": "MONDO:0016529", "names": ["double urethra", "Double urethra", "urethra; double", "double; urethra", "urethra duplication", "urethral duplication", "Duplication of urethra", "duplication of urethra", "Double urethra (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "duplication of urethra", "shortest_name_length": 14}
{"curie": "MONDO:0017856", "names": ["X-linked spasticity-intellectual disability-epilepsy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked spasticity-intellectual disability-epilepsy syndrome", "shortest_name_length": 61}
{"curie": "MONDO:0036025", "names": ["toxicity to dolutegravir"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "toxicity to dolutegravir", "shortest_name_length": 24}
{"curie": "UMLS:C5447393", "names": ["Locally Advanced Lung Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Lung Neuroendocrine Neoplasm", "shortest_name_length": 45}
{"curie": "MONDO:0006027", "names": ["breast synovial sarcoma", "breast synovial sarcoma (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast synovial sarcoma", "shortest_name_length": 23}
{"curie": "MONDO:0032907", "names": ["LMPHM8", "LYMPHATIC MALFORMATION 8", "lymphatic malformation 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphatic malformation 8", "shortest_name_length": 6}
{"curie": "UMLS:C4683567", "names": ["Lugano Classification Stage I Adult Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage I Adult Lymphoma AJCC v8", "shortest_name_length": 52}
{"curie": "MONDO:0033682", "names": ["skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome", "shortest_name_length": 71}
{"curie": "MONDO:0021943", "names": ["tuberculoma", "Tuberculoma", "tuberculomas", "Tuberculomas", "Tuberculoma, NOS", "Tuberculoma (disorder)", "tuberculoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tuberculoma", "shortest_name_length": 11}
{"curie": "MONDO:0018716", "names": ["PICH", "Partially Involuting Congenital Hemangioma", "partially involuting congenital hemangioma", "Partially involuting congenital hemangioma", "Partially involuting congenital haemangioma", "Partially involuting congenital hemangioma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partially involuting congenital hemangioma", "shortest_name_length": 4}
{"curie": "UMLS:C0740406", "names": ["Irreducible hernia", "hernia; irreducible", "HERNIA INCARCERATED", "hernias irreducible", "Incarcerated hernia", "hernia incarcerated", "irreducible; hernia", "Hernia incarcerated", "incarcerated hernia", "hernia; incarcerated", "incarcerated; hernia", "hernias incarcerated", "Incarcerated hernia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Incarcerated hernia", "shortest_name_length": 18}
{"curie": "UMLS:C2367455", "names": ["Relapsed Acute Megakaryoblastic Leukemia", "Recurrent Acute Megakaryoblastic Leukemia", "acute megakaryoblastic leukemia in relapse", "Acute megakaryoblastic leukemia, in relapse", "acute megakaryoblastic leukemia in relapse (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute megakaryoblastic leukemia in relapse", "shortest_name_length": 40}
{"curie": "UMLS:C0270191", "names": ["Neonatal intraventricular bleeding", "Intraventricular hemorrhage neonatal", "neonatal intraventricular hemorrhage", "Neonatal intraventricular hemorrhage", "Perinatal Intraventricular Hemorrhage", "Neonatal intraventricular haemorrhage", "Perinatal intraventricular hemorrhage", "HEMORRHAGE, INTRAVENTRICULAR, NEWBORN", "Intraventricular haemorrhage neonatal", "Perinatal intraventricular haemorrhage", "hemorrhage; intraventricular, fetus or newborn", "Intraventricular hemorrhage of fetus or newborn", "neonatal intraventricular hemorrhage (diagnosis)", "Perinatal intraventricular hemorrhage (disorder)", "Intraventricular hemorrhage from any perinatal cause", "Intraventricular haemorrhage from any perinatal cause"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perinatal intraventricular hemorrhage", "shortest_name_length": 34}
{"curie": "UMLS:C3160769", "names": ["Major bleed"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Major bleed", "shortest_name_length": 11}
{"curie": "UMLS:C0877584", "names": ["Tumor bleeding", "Tumour bleeding", "Tumor hemorrhage", "Tumour haemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tumour haemorrhage", "shortest_name_length": 14}
{"curie": "UMLS:C0333994", "names": ["Ductal Hyperplasia", "Intraductal hyperplasia", "intraductal hyperplasia", "Intraductal Hyperplasia", "Hyperplasia, intraductal", "Intraductal hyperplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraductal Hyperplasia", "shortest_name_length": 18}
{"curie": "MONDO:0016249", "names": ["hereditary site-specific ovarian cancer syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary site-specific ovarian cancer syndrome", "shortest_name_length": 48}
{"curie": "UMLS:C3163625", "names": ["bleeding during pregnancy", "Vaginal Bleeding during Pregnancy", "vaginal bleeding during pregnancy", "Vaginal bleeding during pregnancy", "bleeding during pregnancy (symptom)", "Bleeding from female genital tract during pregnancy", "Bleeding from female genital tract co-occurrent with pregnancy", "Bleeding from female genital tract co-occurrent with pregnancy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vaginal bleeding during pregnancy", "shortest_name_length": 25}
{"curie": "MONDO:0020583", "names": ["chromosome 17 disorder", "chromosome 17 abnormality"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 17 disorder", "shortest_name_length": 22}
{"curie": "MONDO:0001331", "names": ["Conjunctival deposit", "CONJUNCTIVAL DEPOSIT", "conjunctival deposit", "conjunctiva; deposit", "conjunctival deposits", "Conjunctival deposits", "deposition; conjunctiva", "Conjunctival deposit, NOS", "Conjunctival deposit (disorder)", "conjunctival deposits (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "conjunctival deposit", "shortest_name_length": 20}
{"curie": "MONDO:0021367", "names": ["CML AGGRESSIVE", "CML ACCELERATED", "Aggressive-Phase CML", "Accelerated Phase CML", "accelerated phase CGL", "accelerated phase CML", "CML, accelerated phase", "CGL, accelerated phase", "accelerated phase myeloid leukemia", "Leukemia, Myeloid, Aggressive-Phase", "leukemia, myeloid, accelerated-phase", "Leukemia, Myeloid, Accelerated-Phase", "Leukemia, Myeloid, Accelerated Phase", "Leukemia, Myelogenous, Aggressive-Phase", "Leukemia, Myelogenous, Aggressive Phase", "Aggressive-Phase Chronic Myeloid Leukemia", "Accelerated Phase Chronic Myeloid Leukemia", "Accelerated phase chronic myeloid leukemia", "Accelerated phase chronic myeloid leukaemia", "Myeloid Leukemia, Chronic, Aggressive Phase", "Myeloid Leukemia, Chronic, Aggressive-Phase", "Myeloid Leukemia, Chronic, Accelerated-Phase", "Aggressive-Phase Chronic Myelocytic Leukemia", "chronic myeloid leukemia - accelerated phase", "Myeloid Leukemia, Chronic, Accelerated Phase", "Aggressive-Phase Chronic Myelogenous Leukemia", "Accelerated Phase Chronic Myelocytic Leukemia", "Accelerated Phase Chronic Myelogenous Leukemia", "myelocytic leukemia, accelerated phase chronic", "accelerated phase chronic myelogenous leukemia", "chronic myelocytic leukemia, accelerated phase", "accelerated adult chronic myelogenous leukemia", "chronic myelogenous leukemia, accelerated phase", "Accelerated Phase Chronic Granulocytic Leukemia", "myelogenous leukemia, accelerated phase chronic", "Myelogenous Leukemia, Chronic, Aggressive Phase", "Myelogenous Leukemia, Chronic, Aggressive-Phase", "leukemia, accelerated phase chronic myelogenous", "chronic granulocytic leukemia, accelerated phase", "granulocytic leukemia, accelerated phase chronic", "leukemia myelogenous chronic - accelerated phase", "Accelerated phase chronic myeloid leukemia (disorder)", "chronic myeloid leukemia - accelerated phase (diagnosis)", "Accelerated Phase Chronic Myelogenous Leukemia, BCR-ABL1 Positive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukemia, myeloid, accelerated-phase", "shortest_name_length": 14}
{"curie": "MONDO:0017174", "names": ["SCA3, Joseph type", "Azorean disease, type I", "azorean disease, type i", "Machado-Joseph disease type 1", "Azorean disease, type I (disorder)", "spinocerebellar ataxia type 3, Joseph type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Machado-Joseph disease type 1", "shortest_name_length": 17}
{"curie": "UMLS:C0018962", "names": ["hemosalpinx", "hematosalpinx", "HEMATOSALPINX", "Hematosalpinx", "Haematosalpinx", "Hematosalpinx (disorder)", "hematosalpinx (diagnosis)", "Bleeding into fallopian tube"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hematosalpinx", "shortest_name_length": 11}
{"curie": "UMLS:C4745016", "names": ["Recurrent Acute Myeloid Leukemia with t (9;11) (p21.3; q23.3); MLLT3-MLL", "Relapsed Acute Myeloid Leukemia with t (9;11) (p21.3; q23.3); MLLT3-KMT2A", "Recurrent Acute Myeloid Leukemia with t (9;11) (p22.3; q23.3); MLLT3-KMT2A", "Recurrent Acute Myeloid Leukemia with t (9;11) (p21.3; q23.3); MLLT3-KMT2A", "Recurrent Acute Myeloid Leukemia with t (9;11) (p21.3; q23.3); MLLT3 (AF9)-KMT2A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Acute Myeloid Leukemia with t (9;11) (p21.3; q23.3); MLLT3-MLL", "shortest_name_length": 72}
{"curie": "MONDO:0004969", "names": ["acute quadriplegic myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute quadriplegic myopathy", "shortest_name_length": 27}
{"curie": "MONDO:0016198", "names": ["qualitative or quantitative defects of plectin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of plectin", "shortest_name_length": 46}
{"curie": "MONDO:0022645", "names": ["cardioencephalomyopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardioencephalomyopathy", "shortest_name_length": 23}
{"curie": "MONDO:0001941", "names": ["blind", "Blind", "Blindness", "BLINDNESS", "blindness", "Cannot see", "VISION LOSS", "vision loss", "blind vision", "Unable to see", "Blindness NOS", "Blindness, NOS", "Loss of vision", "Legal blindness", "legal blindness", "BLINDNESS LEGAL", "Legal Blindness", "Visual loss, NOS", "Blindness, Legal", "Blindness, legal", "visual impairment", "vision impairment", "Total vision loss", "UTS - Unable to see", "low vision blindness", "blindness (disorder)", "blindness low vision", "Blindness and low vision", "Legal blindness (disorder)", "blindness or low vision (non-specific)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blindness (disorder)", "shortest_name_length": 5}
{"curie": "MONDO:0023015", "names": ["duodenal atresia tetralogy of fallot"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "duodenal atresia tetralogy of fallot", "shortest_name_length": 36}
{"curie": "UMLS:C0162385", "names": ["Pertrochanteric fracture", "fracture intertrochanteric", "Intertrochanteric fracture", "intertrochanteric fracture", "TROCHANTERIC FEMUR FRACTURE", "intertrochanteric fractures", "Intertrochanteric Fractures", "Fractures, Intertrochanteric", "trochanteric fracture of femur", "femur fracture intertrochanteric", "FEMUR INTERTROCHANTERIC FRACTURE", "fracture; femur, pertrochanteric", "Intertrochanteric Femur Fracture", "femur; fracture, pertrochanteric", "Pertrochanteric fracture of femur", "femur fractures intertrochanteric", "femur; fracture, intertrochanteric", "Intertrochanteric femoral fracture", "intertrochanteric fracture of femur", "Pertrochanteric fracture (disorder)", "intertrochanteric; femoral fracture", "Intertrochanteric fracture of femur", "Intertrochanteric fracture (disorder)", "fracture of neck of femur trochanteric", "Trochanteric fracture of neck of femur", "Extracapsular fracture of neck of femur", "Pertrochanteric fracture of neck of femur", "trochanteric fracture of femur (diagnosis)", "fracture of neck of femur intertrochanteric", "Pertrochanteric fracture of femur (diagnosis)", "intertrochanteric fracture of femur (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intertrochanteric Fractures", "shortest_name_length": 24}
{"curie": "MONDO:0100035", "names": ["structural epilepsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "structural epilepsy", "shortest_name_length": 19}
{"curie": "MONDO:0020070", "names": ["neonatal epilepsy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal epilepsy syndrome", "shortest_name_length": 26}
{"curie": "UMLS:C1266034", "names": ["Bronchiolo-alveolar carcinoma, Clara cell", "Non-Mucinous Bronchioloalveolar Carcinoma", "Bronchiolo-alveolar carcinoma, non-mucinous", "Non-Mucinous Bronchoalveolar Lung Carcinoma", "Non-Mucinous Bronchioloalveolar Lung Carcinoma", "Bronchiolo-alveolar carcinoma, type II pneumocyte", "Minimally Invasive Lung Non-Mucinous Adenocarcinoma", "Non-Mucinous Minimally Invasive Lung Adenocarcinoma", "Bronchiolo-alveolar carcinoma, non-mucinous (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bronchiolo-alveolar carcinoma, non-mucinous", "shortest_name_length": 41}
{"curie": "MONDO:0013321", "names": ["FWS", "FORSYTHE-WAKELING SYNDROME", "FORSYTHE-WAKELING syndrome", "forsythe-wakeling syndrome", "microcephaly and Growth retardation with childhood-onset nephrotic syndrome and thrombocytopenia", "MICROCEPHALY AND GROWTH RETARDATION WITH CHILDHOOD-ONSET NEPHROTIC SYNDROME AND THROMBOCYTOPENIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "forsythe-wakeling syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C4724097", "names": ["Grade 3 Ovarian Teratoma", "Malignant Ovarian Teratoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Ovarian Teratoma", "shortest_name_length": 24}
{"curie": "UMLS:C4721779", "names": ["stage IV ovary cancer", "ovary cancer, stage IV", "Ovarian cancer stage IV", "ovarian cancer stage iv", "stage iv ovarian cancer", "stage IV ovarian cancer", "metastatic ovary cancer", "cancer iv ovarian stage", "ovarian cancer, stage IV", "ovary cancer, metastatic", "metastatic ovarian cancer", "Ovarian cancer metastatic", "ovarian cancer, metastatic", "Ovarian epithelial cancer stage IV", "stage IV ovarian epithelial cancer", "ovarian epithelial cancer, stage IV", "metastatic ovarian epithelial cancer", "Ovarian epithelial cancer metastatic", "ovarian epithelial cancer, metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian cancer stage IV", "shortest_name_length": 21}
{"curie": "UMLS:C4528588", "names": ["Stage III Breast Cancer", "Prognostic Stage III Breast Cancer AJCC v8", "Prognostic Stage III Breast Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prognostic Stage III Breast Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "UMLS:C2987256", "names": ["Poorly Differentiated Esophageal Squamous Cell Cancer", "Esophageal Poorly Differentiated Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Poorly Differentiated Squamous Cell Carcinoma", "shortest_name_length": 53}
{"curie": "UMLS:C1335705", "names": ["Recurrent Male Reproductive System Cancer", "Recurrent Male Reproductive System Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Male Reproductive System Carcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0017598", "names": ["C-ALCL", "primary C-ALCL", "Primary C-ALCL", "ALCL, cutaneous", "Primary Cutaneous CD30+ ALCL", "primary cutaneous CD30+ ALCL", "Regressive atypical histiocytosis", "regressive atypical histiocytosis", "Primary cutaneous CD30+ large T-cell lymphoma", "Primary Anaplastic Large Cell Lymphoma of Skin", "primary anaplastic large cell lymphoma of skin", "Primary cutaneous anaplastic large cell lymphoma", "primary cutaneous anaplastic large cell lymphoma", "Primary Cutaneous Anaplastic Large Cell Lymphoma", "Lymphoma, Primary Cutaneous Anaplastic Large Cell", "Primary Anaplastic Large Cell Lymphoma of the Skin", "primary anaplastic large cell lymphoma of the skin", "Cutaneous T-cell lymphoma, large cell, CD30-positive", "Primary cutaneous CD30-positive large T-cell lymphoma", "Primary Cutaneous CD30-positive Large T-Cell Lymphoma", "Primary Cutaneous CD30 positive Large T Cell Lymphoma", "anaplastic large-cell lymphoma, primary cutaneous type", "Primary Cutaneous CD30+ Anaplastic Large Cell Lymphoma", "Anaplastic large-cell lymphoma, primary cutaneous type", "primary cutaneous CD30+ anaplastic large cell lymphoma", "pcALCL - primary cutaneous anaplastic large cell lymphoma", "Primary cutaneous anaplastic large cell lymphoma (disorder)", "Primary cutaneous CD30 antigen positive large T-cell lymphoma", "Primary Cutaneous CD30 Positive Anaplastic Large Cell Lymphoma", "primary cutaneous CD30 Positive anaplastic large cell lymphoma", "Primary cutaneous anaplastic large T-cell lymphoma, CD30-positive", "Anaplastic large cell lymphoma, T/Null cell, primary cutaneous type", "Primary cutaneous CD30 antigen positive large T-cell lymphoma (disorder)", "Primary cutaneous anaplastic large T-cell lymphoma, CD30-positive (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary cutaneous anaplastic large cell lymphoma", "shortest_name_length": 6}
{"curie": "MONDO:0019614", "names": ["pituitary deficiency due to Rathke's cleft cysts", "pituitary deficiency due to Rathke's pouch cysts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pituitary deficiency due to Rathke's pouch cysts", "shortest_name_length": 48}
{"curie": "UMLS:C0346990", "names": ["Carcinomatosis peritonei", "Abdominal Carcinomatosis", "Peritoneal carcinomatosis", "Peritoneal Carcinomatosis", "Peritoneal Carcinomatoses", "peritoneal carcinomatosis", "peritoneum; carcinomatosis", "Carcinomatosis, Peritoneal", "carcinomatosis; peritoneum", "Carcinomatosis of peritoneum", "Peritoneal Surface Malignancy", "Malignancy, Peritoneal Surface", "Surface Malignancy, Peritoneal", "Peritoneal Surface Malignancies", "Carcinomatosis of the Peritoneum", "Carcinomatosis of peritoneal cavity", "Carcinomatosis of peritoneum (disorder)", "Carcinomatosis of peritoneal cavity (disorder)", "Carcinomatosis of peritoneal cavity (diagnosis)", "peritoneal neoplasm malignant secondary carcinomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carcinomatosis of peritoneal cavity", "shortest_name_length": 24}
{"curie": "UMLS:C0156216", "names": ["Gallbladder fistula", "gallbladder fistula", "Gallbladder Fistula", "gallbladder; fistula", "fistula; gallbladder", "fistula of gallbladder", "Fistula of gallbladder", "Fistula of gallbladder, NOS", "gallbladder fistula (diagnosis)", "Fistula of gallbladder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fistula of gallbladder", "shortest_name_length": 19}
{"curie": "UMLS:C1112525", "names": ["Gastrointestinal ulcer bleeding", "Gastrointestinal ulcer hemorrhage", "Gastrointestinal ulcer haemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal ulcer hemorrhage", "shortest_name_length": 31}
{"curie": "EFO:1002029", "names": ["chronic rhinosinusitis with nasal polyps"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic rhinosinusitis with nasal polyps", "shortest_name_length": 40}
{"curie": "MONDO:0006835", "names": ["MCNS", "NIL DISEASE", "Nil disease", "nil disease", "Nil Disease", "disease nils", "Lipid nephrosis", "nephrosis lipoid", "Lipoid Nephrosis", "Lipoid nephrosis", "Lipoid Nephroses", "lipoid nephrosis", "NEPHROSIS, LIPOID", "Nephrosis, lipoid", "lipoid; nephrosis", "Nephroses, Lipoid", "Nephrosis, Lipoid", "nephrosis; lipoid", "Nil change disease", "FOOT PROCESS DISEASE", "Foot-process disease", "Foot process disease", "Minimal Change Disease", "Minimal change disease", "minimal change disease", "MINIMAL CHANGE DISEASE", "change disease minimal", "Minimal Change Diseases", "Disease, Minimal Change", "change diseases minimal", "Epithelial-cell disease", "Diseases, Minimal Change", "Change Diseases, Minimal", "minimal change nephropathy", "Minimal change nephropathy", "Minimal Change Nephropathy", "MINIMAL CHANGE NEPHROPATHY", "Nephropathy, Minimal Change", "MCD - Minimal change disease", "Minimal Change Nephropathies", "idiopathic nephrotic syndrome", "Minimal Change Glomerulopathy", "minimal change glomerulopathy", "Idiopathic nephrotic syndrome", "Nephropathies, Minimal Change", "MINIMAL CHANGE GLOMERULOPATHY", "Glomerulopathy, Minimal Change", "Glomerulopathies, Minimal Change", "MCN - Minimal change nephropathy", "minimal change glomerulonephritis", "minimal change nephrotic syndrome", "Minimal change glomerular disease", "Light negative glomerulonephritis", "change glomerulonephritis minimal", "Minimal change nephrotic syndrome", "Minimal Change Glomerulonephritis", "Glomerulonephritis minimal lesion", "Minimal change disease (disorder)", "Minimal Change Nephrotic Syndrome", "glomerulonephritis minimal change", "Minimal change glomerulonephritis", "changes glomerulonephritis minimal", "Nephrotic Syndrome, Minimal Change", "MCGN - Minimal change glomerulonephritis", "MCNS - Minimal change nephrotic syndrome", "Minimal lesion glomerulonephritis syndrome", "Idiopathic Minimal Change Nephrotic Syndrome", "idiopathic minimal change nephrotic syndrome", "Minimal change glomerulonephritis (diagnosis)", "Nephrotic syndrome with lesion of minimal change glomerulitis", "Nephrotic Syndrome with Lesion of Minimal Change Glomerulonephritis", "Nephrotic syndrome with lesion of minimal change nephrotic syndrome", "Nephrotic syndrome with lesion of minimal change glomerular disease", "Nephrotic syndrome with lesion of minimal change glomerulonephritis", "nephrotic syndrome with lesion of minimal change nephrotic syndrome", "nephrotic syndrome with lesion of minimal change glomerulonephritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lipoid nephrosis", "shortest_name_length": 4}
{"curie": "UMLS:C3888478", "names": ["Medical device site swelling"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Medical device site swelling", "shortest_name_length": 28}
{"curie": "MONDO:0000736", "names": ["DUH", "Freckle", "freckle", "ephelis", "Ephelis", "melanism", "FRECKLES", "Freckles", "Melanism", "freckles", "melanose", "ephelides", "melanosis", "Freckling", "Sun spots", "Melanosis", "MELANOSIS", "EPHELIDES", "Melanoses", "Ephelides", "freckle(s)", "Melanosis, NOS", "Macula solaris", "Focal melanosis", "Melanotic macule", "melanotic macule", "Ephelis (disorder)", "Melanosis (disorder)", "ephelides (diagnosis)", "dyschromatosis universalis", "Dyschromatosis universalis", "Melanosis (morphologic abnormality)", "Dyschromatosis universalis (disorder)", "Dyschromatosis Universalis Hereditaria", "Dyschromatosis universalis hereditaria", "dyschromatosis universalis hereditaria", "Focal melanosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyschromatosis universalis hereditaria", "shortest_name_length": 3}
{"curie": "MONDO:0008474", "names": ["autosomal dominant spondyloepiphyseal dysplasia tarda", "SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL DOMINANT", "Spondyloepiphyseal Dysplasia Tarda, Autosomal Dominant", "spondyloepiphyseal dysplasia tarda, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepiphyseal dysplasia tarda, autosomal dominant", "shortest_name_length": 53}
{"curie": "UMLS:C3898126", "names": ["Non-Neoplastic Muscle Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Muscle Disorder", "shortest_name_length": 30}
{"curie": "MONDO:0007985", "names": ["metatarsus varus, type 1", "metatarsus varus, type I", "Metatarsus Varus, Type I", "METATARSUS VARUS, TYPE I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metatarsus varus, type 1", "shortest_name_length": 24}
{"curie": "MONDO:0021533", "names": ["intestine NET G1", "Intestinal NET G1", "intestinal NET G1", "Intestine Carcinoid Tumor", "carcinoid intestine tumor", "intestine carcinoid tumor", "Intestinal Carcinoid Tumor", "intestinal carcinoid tumor", "carcinoid intestines tumors", "carcinoid tumor of intestine", "Carcinoid tumor of intestine", "Carcinoid Tumor of Intestine", "CARCINOID TUMORS, INTESTINAL", "Carcinoid Tumors, Intestinal", "Carcinoid tumour of intestine", "carcinoid tumor of the intestine", "Carcinoid Tumor of the Intestine", "intestinal neuroendocrine tumor G1", "Intestinal Neuroendocrine Tumor G1", "intestine carcinoid tumor (disease)", "intestine neuroendocrine neoplasm G1", "Carcinoid tumor of intestine (disorder)", "Carcinoid tumor of intestine (diagnosis)", "grade 1 neuroendocrine neoplasm of intestine", "neoplasm of gastrointestinal tract carcinoid tumor intestine", "intestine neuroendocrine tumor, well differentiated, low grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intestinal neuroendocrine tumor G1", "shortest_name_length": 16}
{"curie": "UMLS:C3854116", "names": ["Lipodystrophy due to Human immunodeficiency virus infection and antiretroviral therapy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lipodystrophy due to Human immunodeficiency virus infection and antiretroviral therapy", "shortest_name_length": 86}
{"curie": "UMLS:C3899638", "names": ["Undifferentiated Pleomorphic Sarcoma", "Childhood Malignant Fibrous Histiocytoma", "Childhood Unclassified Pleomorphic Sarcoma", "Childhood Undifferentiated Pleomorphic Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Undifferentiated Pleomorphic Sarcoma", "shortest_name_length": 36}
{"curie": "MONDO:0009192", "names": ["WRS", "Iddm-Med syndrome", "MED-IDDM syndrome", "Med-Iddm syndrome", "MED-IDDM SYNDROME", "IDDM-MED SYNDROME", "IDDM-MED syndrome", "WOLCOTT-RALLISON SYNDROME", "Wolcott-Rallison syndrome", "Wolcott Rallison syndrome", "Wolcott-Rallison Syndrome", "Wolcott-Rallison dysplasia", "Wolcott-Rallison dysplasia (disorder)", "spondylo-epiphyseal dysplasia-diabetes mellitus syndrome", "early-onset diabetes mellitus-epiphyseal dysplasia syndrome", "early-onset diabetes mellitus with multiple epiphyseal dysplasia", "Early-onset diabetes mellitus with multiple epiphyseal dysplasia", "epiphyseal dysplasia multiple with early-onset diabetes mellitus", "Epiphyseal dysplasia, multiple, with early-onset diabetes mellitus", "epiphyseal dysplasia, multiple, with early-onset diabetes mellitus", "Epiphyseal dysplasia, multiple, with early onset diabetes mellitus", "EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS", "multiple epiphyseal dysplasia-early onset diabetes mellitus syndrome", "infancy-onset diabetes mellitus-multiple epiphyseal dysplasia syndrome", "multiple epiphyseal dysplasia-early onset diabetes mellitus (MED-IDDM) syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wolcott-Rallison syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C4763424", "names": ["Recurrent Paraganglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Paraganglioma", "shortest_name_length": 23}
{"curie": "UMLS:C0409651", "names": ["Seropositive RA", "rheumatoid arthritis RF positive", "rheumatoid/seropositive arthritis", "Seropositive Rheumatoid Arthritis", "rheumatoid arthritis seropositive", "Seropositive rheumatoid arthritis", "arthritis rheumatoid seropositive", "Rheumatoid/seropositive arthritis", "arthritis; rheumatoid, seropositive", "rheumatoid; arthritis, seropositive", "Rheumatoid arthritis/allied condition", "rheumatoid arthritis RF positive (diagnosis)", "Seropositive rheumatoid arthritis (disorder)", "unspecified seropositive rheumatoid arthritis", "Seropositive rheumatoid arthritis (diagnosis)", "Seropositive rheumatoid arthritis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Seropositive rheumatoid arthritis", "shortest_name_length": 15}
{"curie": "UMLS:C4087141", "names": ["Metastatic Skin Squamous Cell Carcinoma", "Skin squamous cell carcinoma metastatic", "Metastatic Cutaneous Squamous Cell Carcinoma", "metastatic squamous cell carcinoma of the skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin squamous cell carcinoma metastatic", "shortest_name_length": 39}
{"curie": "UMLS:C0242013", "names": ["NEURITIS SCIATIC", "Neuritis sciatic", "Sciatic Neuritis", "neuritis sciatic", "sciatic neuritis", "NEURITIS, SCIATIC", "Neuritis, Sciatic", "Sciatic Neuritides", "Neuritides, Sciatic", "sciatic neuritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sciatic Neuritis", "shortest_name_length": 16}
{"curie": "MONDO:0010630", "names": ["imprinting gene related to retinoblastoma", "IMPRINTING GENE RELATED TO RETINOBLASTOMA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "imprinting gene related to retinoblastoma", "shortest_name_length": 41}
{"curie": "MONDO:0005538", "names": ["rectitis", "Proctitis", "PROCTITIS", "proctitis", "Proctitides", "Proctitis NOS", "Proctitis, NOS", "Rectum inflamed", "anus inflammation", "rectal inflammation", "RECTAL INFLAMMATION", "ulcerative proctitis", "Proctitis (disorder)", "inflammation of anus", "proctitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "proctitis", "shortest_name_length": 8}
{"curie": "MONDO:0018165", "names": ["VTOS", "Venous TOS", "Paget-Schrotter disease", "Paget Schrotter disease", "Venous cervical rib syndrome", "Venous hyperabduction syndrome", "venous thoracic outlet syndrome", "Venous costoclavicular syndrome", "Venous thoracic outlet syndrome", "Venous Thoracic Outlet Syndrome", "Venous scalenus anticus syndrome", "Effort subclavian vein thrombosis", "effort subclavian vein thrombosis", "Venous thoracic outlet syndrome (disorder)", "Venous thoracic outlet compression syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "venous thoracic outlet syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0586355", "names": ["Mild esophageal dysplasia", "Mild oesophageal dysplasia", "Esophageal Low Grade Dysplasia", "Mild esophageal dysplasia (disorder)", "Esophageal Low Grade Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mild esophageal dysplasia", "shortest_name_length": 25}
{"curie": "MONDO:0010075", "names": ["SEMDJL", "SEMDJL1", "SEMD-JL", "Spondyloepimetaphyseal dysplasia with joint laxity", "spondyloepimetaphyseal dysplasia with joint laxity type 1", "Spondyloepimetaphyseal dysplasia with joint laxity type 1", "SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1", "B3GALT6 spondyloepimetaphyseal dysplasia with joint laxity", "Spondyloepimetaphyseal dysplasia with joint laxity, Beighton type", "spondyloepimetaphyseal dysplasia with joint laxity caused by mutation in B3GALT6", "spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures", "SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES", "spondyloepimetaphyseal dysplasia with JOINT laxity, type 1, with or without fractures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures", "shortest_name_length": 6}
{"curie": "UMLS:C0280303", "names": ["Lower Gum SCC", "SCC of Lower Gum", "Lower Gingival SCC", "SCC of Lower Gingiva", "SCC of the Lower Gum", "SCC of the Lower Gingiva", "Lower Gum Squamous Cell Carcinoma", "Squamous Cell Carcinoma of Lower Gum", "Lower Gingival Squamous Cell Carcinoma", "Squamous Cell Carcinoma of the Lower Gum", "Squamous Cell Carcinoma of Lower Gingiva", "Squamous Cell Carcinoma of the Lower Gingiva"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lower Gingival Squamous Cell Carcinoma", "shortest_name_length": 13}
{"curie": "UMLS:C0279956", "names": ["Stage I Grade 3 Follicular Lymphoma", "stage I grade 3 follicular lymphoma", "Grade III Follicular Lymphoma Stage I", "Follicular Lymphoma Grade III Stage I", "Stage I Grade III Follicular Lymphoma", "Follicular Large Cell Lymphoma Stage I", "Stage I Follicular Large Cell Lymphoma", "stage I follicular large cell lymphoma", "follicular large cell lymphoma, stage I", "Ann Arbor Stage I Grade 3 Follicular Lymphoma", "Stage I Grade III Follicular Large Cell Lymphoma", "stage I grade III follicular large cell lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage I Grade 3 Follicular Lymphoma", "shortest_name_length": 35}
{"curie": "MONDO:0003725", "names": ["adenosis", "adenosis breast", "breast adenosis", "Breast Adenosis", "adenosis - breast", "Adenosis - breast", "adenosis of breast", "Adenosis of Breast", "breast fibroadenosis", "FIBROADENOSIS BREAST", "Breast fibroadenosis", "Fibroadenosis breast", "BREAST FIBROADENOSIS", "fibroadenosis; breast", "adenofibrosis; breast", "Adenosis of the Breast", "adenosis of the breast", "Adenosis of the breast", "Fibroadenosis - breast", "fibroadenosis of breast", "microglandular adenosis", "Fibroadenosis of breast", "Microglandular Adenoses", "Microglandular Adenosis", "Adenofibrosis of breast", "Adenosis, Microglandular", "Adenoses, Microglandular", "Fibroadenosis of breast NOS", "Fibroadenosis of breast, NOS", "Fibroadenosis of breast (disorder)", "fibroadenosis of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast adenosis", "shortest_name_length": 8}
{"curie": "MONDO:0016305", "names": ["PKAN, atypical form", "NBIA1, atypical form", "atypical pantothenate kinase-associated neurodegeneration", "neurodegeneration with brain iron accumulation type 1, atypical form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical pantothenate kinase-associated neurodegeneration", "shortest_name_length": 19}
{"curie": "MONDO:0700192", "names": ["chicken hepatoma", "Chicken Hepatoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chicken hepatoma", "shortest_name_length": 16}
{"curie": "MONDO:0007339", "names": ["BCDS", "BCDS1", "BCD SYNDROME", "BCD syndrome", "Elsching syndrome", "Elschnig syndrome", "ELSCHNIG SYNDROME", "BLEPHAROCHEILODONTIC SYNDROME", "blepharocheilodontic syndrome", "Blepharocheilodontic syndrome", "blepharo-cheilo-dontic syndrome", "blepharocheilodontic syndrome 1", "Blepharo-cheilo-dontic syndrome", "Blepharo-cheilo-odontic syndrome", "blepharo-cheilo-odontic syndrome", "CLEFTING, ECTROPION, AND CONICAL TEETH", "clefting, ectropion, and conical teeth", "Clefting, ectropion, and conical teeth", "Blepharocheilodontic syndrome (disorder)", "Clefting-ectropion-conical teeth syndrome", "clefting-ectropion-conical teeth syndrome", "ectropion inferior cleft lip and or palate", "Lagophthalmia-cleft lip and palate syndrome", "Clefting, ectropion, conical teeth syndrome", "lagophthalmia-cleft lip and palate syndrome", "ECTROPION, INFERIOR, WITH CLEFT LIP AND/OR PALATE", "Lagophthalmia with bilateral cleft lip and palate", "ectropion, inferior, with cleft lip and/or palate", "LAGOPHTHALMIA WITH BILATERAL CLEFT LIP AND PALATE", "lagophthalmia with bilateral cleft lip and palate", "ectropion inferior-cleft lip and/or palate syndrome", "Ectropion inferior-cleft lip and/or palate syndrome", "ectropion inferior-cleft lip and or palate syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blepharocheilodontic syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C5555540", "names": ["Recurrent Atypical Meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Atypical Meningioma", "shortest_name_length": 29}
{"curie": "MONDO:0013940", "names": ["CILD18", "primary ciliary dyskinesia 18", "ciliary dyskinesia, primary, 18", "CILIARY DYSKINESIA, PRIMARY, 18", "DNAAF5 primary ciliary dyskinesia", "primary ciliary dyskinesia type 18", "ciliary dyskinesia, primary, type 18", "primary ciliary dyskinesia caused by mutation in DNAAF5", "primary ciliary dyskinesia 18 with or without situs inversus", "CILIARY DYSKINESIA, PRIMARY, 18, WITH OR WITHOUT SITUS INVERSUS", "ciliary dyskinesia, primary, 18, with or without situs inversus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia 18", "shortest_name_length": 6}
{"curie": "MONDO:0008489", "names": ["sternum, premature obliteration of sutures of", "STERNUM, PREMATURE OBLITERATION OF SUTURES OF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sternum, premature obliteration of sutures of", "shortest_name_length": 45}
{"curie": "MONDO:0100412", "names": ["AML, moCEBPA", "AML, CEBPA Monoallelic Mutation", "AML, CEBP Monoallelic Gene Mutation", "AML, monoallelic CEBPA gene mutation", "AML, CEBPA Monoallelic Gene Mutation", "AML, C/EBPalpha Monoallelic Gene Mutation", "AML, C/EBP-Alpha Monoallelic Gene Mutation", "acute myeloid leukemia, monoallelic CEBPA gene mutation", "AML, CCAAT Enhancer Binding Protein Alpha Monoallelic Gene Mutation", "AML, CCAAT/Enhancer Binding Protein Alpha Monoallelic Gene Mutation", "AML, CCAAT/Enhancer Binding Protein, Alpha Monoallelic Gene Mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, monoallelic CEBPA gene mutation", "shortest_name_length": 12}
{"curie": "MONDO:0016065", "names": ["Mathieu-De Broca-Bony syndrome", "Mathieu De Broca Bony syndrome", "cleft palate short stature vertebral anomalies", "Cleft palate-short stature-vertebral anomalies syndrome", "cleft palate-short stature-vertebral anomalies syndrome", "Cleft palate with short stature and vertebral anomaly syndrome", "cleft palate with short stature and vertebral anomaly syndrome", "Cleft palate with short stature and vertebral anomaly syndrome (disorder)", "cleft palate with short stature and vertebral anomaly syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleft palate-short stature-vertebral anomalies syndrome", "shortest_name_length": 30}
{"curie": "UMLS:C1883353", "names": ["Tobacco Toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tobacco Toxicity", "shortest_name_length": 16}
{"curie": "UMLS:C5555869", "names": ["Intermediate EBS with cardiomyopathy", "Intermediate epidermolysis bullosa simplex with cardiomyopathy", "Intermediate Epidermolysis Bullosa Simplex with Cardiomyopathy", "Intermediate epidermolysis bullosa simplex with cardiomyopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intermediate epidermolysis bullosa simplex with cardiomyopathy", "shortest_name_length": 36}
{"curie": "MONDO:0012428", "names": ["KYPSC1", "kyphoscoliosis 1", "Kyphoscoliosis 1", "KYPHOSCOLIOSIS 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kyphoscoliosis 1", "shortest_name_length": 6}
{"curie": "UMLS:C1334222", "names": ["IR GIST", "Intermediate Risk GIST", "Intermediate Risk Gastrointestinal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intermediate Risk Gastrointestinal Stromal Tumor", "shortest_name_length": 7}
{"curie": "UMLS:C5236092", "names": ["Infiltrating Urothelial Carcinoma, Sarcomatoid Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infiltrating Urothelial Carcinoma, Sarcomatoid Variant", "shortest_name_length": 54}
{"curie": "MONDO:0011762", "names": ["DFNB22", "autosomal recessive deafness 22", "DEAFNESS, AUTOSOMAL RECESSIVE 22", "deafness, autosomal recessive 22", "Deafness, Autosomal Recessive 22", "deafness, autosomal recessive type 22", "autosomal recessive nonsyndromic deafness 22", "OTOA autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 22", "autosomal recessive nonsyndromic deafness type 22", "autosomal recessive nonsyndromic deafness caused by mutation in OTOA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 22", "shortest_name_length": 6}
{"curie": "UMLS:C1332906", "names": ["Cerebral Glioblastoma", "Cerebral Glioblastoma Multiforme", "Hemispheric Glioblastoma Multiforme", "Cerebral Hemisphere Glioblastoma Multiforme", "Glioblastoma Multiforme of Cerebral Hemisphere", "Glioblastoma Multiforme of the Cerebral Hemisphere"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebral Glioblastoma", "shortest_name_length": 21}
{"curie": "MONDO:0025353", "names": ["DEE90", "developmental and epileptic encephalopathy 90", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 90", "developmental and epileptic encephalopathy, 90", "developmental and epileptic encephalopathy 90, X-linked recessive, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 90", "shortest_name_length": 5}
{"curie": "UMLS:C3640031", "names": ["Congenital Phrenic Nerve Palsy", "Phrenic Nerve Palsy, Congenital"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Phrenic Nerve Palsy", "shortest_name_length": 30}
{"curie": "UMLS:C1533659", "names": ["Retinal Detachment and Defect", "Retinal detachments and defects", "retinal detachments and defects", "retinal detachments and defects (diagnosis)", "Retinal detachments and defects, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retinal detachments and defects, unspecified", "shortest_name_length": 29}
{"curie": "UMLS:C0433054", "names": ["BITE WOUND HUMAN", "Human bite - wound", "Human bite - wound (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Human bite - wound", "shortest_name_length": 16}
{"curie": "MONDO:0012259", "names": ["Paraphyseal cyst", "paraphyseal cyst", "Neuroepithelial cyst", "neuroepithelial cyst", "colloid cyst third ventricle", "Third ventricle colloid cyst", "Third Ventricle Colloid Cyst", "Colloid cyst of third ventricle", "Colloid Cyst of Third Ventricle", "colloid cyst of third ventricle", "Colloid cysts of third ventricle", "colloid cysts of third ventricle", "COLLOID CYSTS OF THIRD VENTRICLE", "Third Ventricle Paraphyseal Cyst", "Paraphyseal Cyst of Third Ventricle", "Colloid Cyst of the Third Ventricle", "Third Ventricle Neuroepithelial Cyst", "Paraphyseal Cyst of the Third Ventricle", "Neuroepithelial Cyst of Third Ventricle", "Neuroepithelial cysts of third ventricle", "NEUROEPITHELIAL CYSTS OF THIRD VENTRICLE", "neuroepithelial cysts of third ventricle", "Colloid cyst of third ventricle (disorder)", "Neuroepithelial Cyst of the Third Ventricle", "colloid cyst of third ventricle (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colloid cysts of third ventricle", "shortest_name_length": 16}
{"curie": "UMLS:C1332966", "names": ["desmoplastic small round cell tumor", "Desmoplastic Small Round Cell Tumor", "childhood desmoplastic small round cell tumor", "pediatric desmoplastic small round cell tumor", "Pediatric Desmoplastic Small Round Cell Tumor", "Childhood Desmoplastic Small Round Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Desmoplastic Small Round Cell Tumor", "shortest_name_length": 35}
{"curie": "MONDO:0030335", "names": ["MVID2", "DIAR12", "microvillus inclusion disease 2", "MICROVILLUS INCLUSION DISEASE 2", "diarrhea 12, with microvillus atrophy", "DIARRHEA 12, WITH MICROVILLUS ATROPHY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diarrhea 12, with microvillus atrophy", "shortest_name_length": 5}
{"curie": "UMLS:C0151882", "names": ["Rash purpuric", "RASH PURPITIC", "PURPURIC RASH", "RASH PURPURIC", "purpuric rash", "Purpuric rash", "Purpuric rashes", "Purpuric rash (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Purpuric rash", "shortest_name_length": 13}
{"curie": "UMLS:C4511594", "names": ["cannabis dependence with cannabis hyperemesis syndrome", "cannabis dependence with cannabis hyperemesis syndrome (diagnosis)", "Cannabis hyperemesis syndrome co-occurrent and due to cannabis dependence", "Cannabis hyperemesis syndrome co-occurrent and due to cannabis dependence (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cannabis hyperemesis syndrome co-occurrent and due to cannabis dependence", "shortest_name_length": 54}
{"curie": "UMLS:C0149674", "names": ["elbow injury", "injury elbow", "Elbow Injury", "ELBOW INJURY", "Elbow injury", "elbow; injury", "Injury, Elbow", "injury; elbow", "elbow injuries", "Elbow Injuries", "injury of elbow", "Injury of elbow", "disorders elbow injuries", "Injury of elbow (disorder)", "injury of elbow (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Elbow Injuries", "shortest_name_length": 12}
{"curie": "UMLS:C4525263", "names": ["Stage III Intrahepatic Bile Duct Cancer", "Stage III Intrahepatic Bile Duct Cancer AJCC v8", "Stage III Intrahepatic Bile Duct Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Intrahepatic Bile Duct Cancer AJCC v8", "shortest_name_length": 39}
{"curie": "MONDO:0032620", "names": ["MC1DN15", "nuclear type mitochondrial complex I deficiency 15", "mitochondrial complex 1 deficiency, nuclear type 15", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 15"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 15", "shortest_name_length": 7}
{"curie": "MONDO:0025453", "names": ["Maedi", "Maedi-Visna", "maedi-visna", "maedi visna", "Zwoegersiekte", "ovine progressive pneumonia", "Ovine progressive pneumonia", "progressive pneumonia sheep", "Progressive pneumonia of sheep", "Chronic viral encephalomyelitis of sheep", "Progressive pneumonia of sheep (disorder)", "Progressive Interstitial Pneumonia of Sheep", "progressive interstitial pneumonia of sheep", "pneumonia, progressive interstitial, of sheep", "Pneumonia, Progressive Interstitial, of Sheep"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pneumonia, progressive interstitial, of sheep", "shortest_name_length": 5}
{"curie": "UMLS:C0343869", "names": ["anal thrush", "Anal thrush", "Anus candida", "anal candida", "ANAL CANDIDA", "candida anus", "Anal candida", "Anal candidosis", "Anal candidiasis", "candidiasis anal", "Anal candidiasis (disorder)", "Anal candidiasis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anal candidiasis", "shortest_name_length": 11}
{"curie": "MONDO:0001966", "names": ["chronic closed-angle glaucoma", "chronic narrow angle glaucoma", "Chronic narrow angle glaucoma", "Chronic closed-angle glaucoma", "Chronic angle-closure glaucoma", "chronic angle-closure glaucoma", "angle-closure glaucoma, chronic", "anatomical narrow angle glaucoma", "glaucoma; chronic, angle-closure", "Anatomical narrow angle glaucoma", "chronic; glaucoma, angle-closure", "CNAG - Chronic narrow angle glaucoma", "Anatomical narrow angle glaucoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic closed-angle glaucoma", "shortest_name_length": 29}
{"curie": "UMLS:C5419177", "names": ["COVID-19-Associated Acute Intestinal Injury", "SARS-CoV-2-Associated Acute Intestinal Injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "COVID-19-Associated Acute Intestinal Injury", "shortest_name_length": 43}
{"curie": "UMLS:C1563697", "names": ["Chromosome Instability Syndrome", "Syndrome, Chromosome Instability", "Chromosome Instability Syndromes", "Syndromes, Chromosome Instability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chromosome Instability Syndromes", "shortest_name_length": 31}
{"curie": "UMLS:C1444565", "names": ["Cardiopulmonary failure", "CARDIORESPIRATORY FAILURE", "Cardiorespiratory failure", "cardiorespiratory failure", "Cardio-respiratory failure", "Cardiorespiratory failure (disorder)", "cardiorespiratory failure (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiorespiratory failure", "shortest_name_length": 23}
{"curie": "MONDO:0044715", "names": ["metopic ridging-ptosis-facial dysmorphism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metopic ridging-ptosis-facial dysmorphism syndrome", "shortest_name_length": 50}
{"curie": "UMLS:C5238521", "names": ["Advanced Fallopian Tube Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Fallopian Tube Carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0012685", "names": ["MAFD5", "MAJOR AFFECTIVE DISORDER 5", "Major Affective Disorder 5", "MAJOR affective disorder 5", "bipolar affective disorder", "major affective disorder 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "major affective disorder 5", "shortest_name_length": 5}
{"curie": "MONDO:0032780", "names": ["HIDEA", "HYPOTONIA, HYPOVENTILATION, IMPAIRED INTELLECTUAL DEVELOPMENT, DYSAUTONOMIA, EPILEPSY, AND EYE ABNORMALITIES", "hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities", "HYPOTONIA, HYPERVENTILATION, IMPAIRED INTELLECTUAL DEVELOPMENT, DYSAUTONOMIA, EPILEPSY, AND EYE ABNORMALITIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities", "shortest_name_length": 5}
{"curie": "UMLS:C5419167", "names": ["COVID-19-Associated Acute Hemorrhagic Necrotizing Encephalitis", "SARS-CoV-2-Associated Acute Hemorrhagic Necrotizing Encephalitis", "COVID-19-Associated Acute Hemorrhagic Necrotizing Encephalopathy", "SARS-CoV-2-Associated Acute Hemorrhagic Necrotizing Encephalopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "COVID-19-Associated Acute Hemorrhagic Necrotizing Encephalitis", "shortest_name_length": 62}
{"curie": "UMLS:C5418298", "names": ["Skin Soft Tissue Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin Soft Tissue Neoplasm", "shortest_name_length": 25}
{"curie": "MONDO:0030018", "names": ["AIEFL", "CRIA SYNDROME", "CRIA syndrome", "Cria Syndrome", "autoinflammation with episodic fever and lymphadenopathy", "AUTOINFLAMMATION WITH EPISODIC FEVER AND LYMPHADENOPATHY", "Cleavage-resistant RIPK1-induced autoinflammatory syndrome", "CLEAVAGE-RESISTANT RIPK1-INDUCED AUTOINFLAMMATORY SYNDROME", "Cleavage-Resistant Ripk1-Induced Autoinflammatory Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoinflammation with episodic fever and lymphadenopathy", "shortest_name_length": 5}
{"curie": "MONDO:0018926", "names": ["TSE", "human prion disease", "transmissible spongiform encephalopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "human prion disease", "shortest_name_length": 3}
{"curie": "MONDO:0017238", "names": ["hemoglobinopathy Toms River", "transient neonatal cyanosis and anemia due to Toms River Hemoglobin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemoglobinopathy Toms River", "shortest_name_length": 27}
{"curie": "MONDO:0010873", "names": ["BH", "band heterotopia", "Band Heterotopia of Brain", "band heterotopia of brain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "band heterotopia of brain", "shortest_name_length": 2}
{"curie": "UMLS:C1333150", "names": ["Connective and Soft Tissue Disease", "Connective and Soft Tissue Diseases", "Connective and Soft Tissue Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Connective and Soft Tissue Disorder", "shortest_name_length": 34}
{"curie": "MONDO:0021065", "names": ["pleura tumor", "tumor pleura", "pleural tumor", "Pleural Tumor", "pleura tumors", "Tumor of pleura", "pleura neoplasm", "Tumor of Pleura", "tumor of pleura", "Tumour of pleura", "pleural neoplasm", "Pleural neoplasm", "Pleural Neoplasm", "Pleural Neoplasms", "Pleural neoplasms", "Neoplasm, Pleural", "Neoplasm of pleura", "neoplasm of pleura", "Neoplasm of Pleura", "Neoplasms, Pleural", "Tumor of the Pleura", "tumor of the pleura", "Pleural neoplasm NOS", "pleural cavity tumor", "neoplasm of the pleura", "Neoplasm of the Pleura", "pleura neoplasm (disease)", "neoplasm of pleural cavity", "Neoplasm of pleura (disorder)", "neoplasm of pleura (diagnosis)", "pleural cavity neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pleural neoplasm", "shortest_name_length": 12}
{"curie": "MONDO:0030910", "names": ["MRD45", "autosomal dominant mental retardation 45", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 45", "mental retardation, autosomal dominant 45", "autosomal dominant intellectual disability 45", "intellectual disability, autosomal dominant 45", "autosomal dominant intellectual developmental disorder 45", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 45"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 45", "shortest_name_length": 5}
{"curie": "MONDO:0010167", "names": ["UROCD", "Urocanic aciduria", "urocanic aciduria", "UROCANASE DEFICIENCY", "urocanase deficiency", "Urocanase deficiency", "urocanic aciduria (disease)", "urocanate hydratase deficiency", "Urocanate hydratase deficiency", "High urine urocanic acid levels", "high urine urocanic acid levels", "Urocanate hydratase deficiency (disorder)", "encephalopathy due to urocanase deficiency", "Encephalopathy due to urocanase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urocanic aciduria", "shortest_name_length": 5}
{"curie": "MONDO:0000770", "names": ["Allergy, Seafood", "Shellfish Allergy", "allergy shellfish", "Shellfish allergy", "shellfish allergy", "Allergy, Shellfish", "Shellfish Allergies", "allergies shellfish", "Allergy to shellfish", "Allergies, Shellfish", "FOOD ALLERGY TO SHELLFISH", "Shellfish Hypersensitivity", "Hypersensitivity, Shellfish", "Shellfish Hypersensitivities", "Hypersensitivities, Shellfish", "Allergy to shellfish (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "shellfish allergy", "shortest_name_length": 16}
{"curie": "MONDO:0011116", "names": ["LACHT", "Manouvrier syndrome", "Mardini Nyhan syndrome", "Mardini-Nyhan syndrome", "MARDINI-NYHAN ASSOCIATION", "Mardini-Nyhan association", "Lung agenesis heart defect thumb anomalies", "lung agenesis heart defect thumb anomalies", "pulmonary aplasia and triphalangia of the thumb", "Pulmonary aplasia and triphalangia of the thumb", "Lung agenesis-heart defect-thumb anomalies syndrome", "lung agenesis-heart defect-thumb anomalies syndrome", "Lung agenesis with heart defect and thumb anomaly syndrome", "Lung agenesis with heart defect and thumb anomaly syndrome (disorder)", "LUNG AGENESIS, CONGENITAL HEART DEFECTS, AND THUMB ANOMALIES SYNDROME", "lung agenesis, congenital heart defects, and thumb anomalies syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung agenesis-heart defect-thumb anomalies syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0002480", "names": ["Endometrioid tumor", "endometrioid tumor", "Endometrioid Tumor", "Endometrioid tumour", "endometrioid neoplasm", "Endometrioid Neoplasm", "female reproductive endometrioid tumor", "female reproductive endometrioid cancer", "female reproductive endometrioid neoplasm", "endometrioid tumor (morphologic abnormality)", "Endometrioid tumor (morphologic abnormality)", "endometrioid tumor of female reproductive system", "endometrioid neoplasm of female reproductive system", "endometrioid tumor of the female reproductive system", "endometrioid neoplasm of the female reproductive system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometrioid tumor", "shortest_name_length": 18}
{"curie": "OMIM:611664", "names": ["SHEP7", "Shep7", "Skin/Hair/Eye Pigmentation, Variation In, 7", "Skin-Hair-Eye Pigmentation, Variation In, 7", "SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 7", "SKIN/HAIR/EYE PIGMENTATION 7, DARK/LIGHT SKIN", "Skin-Hair-Eye Pigmentation 7, Dark-Light Skin", "SKIN/HAIR/EYE PIGMENTATION 7, BLOND/BROWN HAIR", "Skin-Hair-Eye Pigmentation 7, Blond-Brown Hair"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 5}
{"curie": "MONDO:0015148", "names": ["LIS3", "lissencephaly 3", "lissencephaly type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lissencephaly type 3", "shortest_name_length": 4}
{"curie": "UMLS:C3899731", "names": ["Calcineurin Nephrotoxicity", "Calcineurin Inhibitor Nephrotoxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Calcineurin Nephrotoxicity", "shortest_name_length": 26}
{"curie": "UMLS:C0278711", "names": ["stage I Wilms tumor", "Stage I Wilms Tumor", "stage I Wilm's tumor", "Wilms tumor, stage I", "stage I Wilms' tumor", "Wilm's tumor, stage I", "Wilms' tumor, stage I", "stage I nephroblastoma", "nephroblastoma, stage I", "Stage I Renal Wilms Tumor", "Stage I Kidney Wilms Tumor", "Stage I Renal Wilms' Tumor", "Stage I Kidney Nephroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Kidney Wilms Tumor", "shortest_name_length": 19}
{"curie": "MONDO:0000608", "names": ["FJHN", "Juvenile gout", "juvenile gout", "Familial juvenile gout", "Familial gout nephropathy", "Precocious adolescent gout", "juvenile gouty nephropathy", "gouty nephropathy, familial", "familial nephropathy with gout", "nephropathy, familial, with gout", "Familial gout with renal failure", "tubulointerstitial kidney disease", "Familial juvenile gout (disorder)", "familial juvenile gouty nephropathy", "Familial juvenile gouty nephropathy", "gouty nephropathy, familial juvenile", "Familial juvenile hyperuricemia nephropathy", "familial juvenile hyperuricemic nephropathy", "Familial juvenile hyperuricaemia nephropathy", "familial nephropathy associated with hyperuricemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial juvenile hyperuricemic nephropathy", "shortest_name_length": 4}
{"curie": "MONDO:0006701", "names": ["Chromophobe adenoma", "Chromophobe Adenoma", "chromophobe adenoma", "adenoma chromophobe", "Chromophobe Adenomas", "Adenoma, Chromophobe", "Adenomas, Chromophobe", "Pituitary Chromophobe Adenoma", "adenoma chromophobe pituitary", "pituitary chromophobe adenoma", "chromophobe adenoma, pituitary", "adenoma, chromophobe, pituitary", "pituitary gland chromophobe adenoma", "Pituitary Gland Chromophobe Adenoma", "chromophobe adenoma of pituitary gland", "Chromophobe Adenoma of Pituitary Gland", "Chromophobe Adenoma of the Pituitary Gland", "chromophobe adenoma of the pituitary gland", "Chromophobe adenoma of the Pituitary gland", "Chromophobe adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromophobe adenoma", "shortest_name_length": 19}
{"curie": "UMLS:C4744801", "names": ["Thyroid Gland Histiocytic and Dendritic Cell Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Histiocytic and Dendritic Cell Neoplasm", "shortest_name_length": 53}
{"curie": "MONDO:0019983", "names": ["multilocular renal cyst", "Multilocular renal cyst", "multiloculated renal cyst", "Multiloculated renal cyst", "Multilocular cyst of the kidney", "multilocular cyst of the kidney", "Solitary multilocular renal cyst", "Solitary multilocular renal cyst (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiloculated renal cyst", "shortest_name_length": 23}
{"curie": "MONDO:0013080", "names": ["PBC3", "Biliary Cirrhosis, Primary, 3", "BILIARY CIRRHOSIS, PRIMARY, 3", "primary biliary cholangitis 3", "biliary cirrhosis, primary, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary biliary cholangitis 3", "shortest_name_length": 4}
{"curie": "MONDO:0018954", "names": ["Loeys-Dietz syndrome", "Loeys-Dietz Syndrome", "Loeys Dietz Syndrome", "Syndrome, Loeys-Dietz", "Loeys-Dietz syndrome (disorder)", "Loeys-Dietz syndrome (diagnosis)", "aortic aneurysm syndrome, Loeys-Dietz type", "Aortic aneurysm syndrome due to TGF-beta receptors anomalies", "aortic aneurysm syndrome due to TGF-beta receptors anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Loeys-Dietz syndrome", "shortest_name_length": 20}
{"curie": "MONDO:0007478", "names": ["KCS2", "Kenny syndrome", "Kenny-Caffey Syndrome Type 2", "Kenny-Caffey syndrome type 2", "Kenny-Caffey syndrome, type 2", "autosomal dominant Kenny-Caffey syndrome", "Kenny-Caffey syndrome, autosomal dominant", "dwarfism, cortical thickening of tubular bones and transient hypocalcemia", "dwarfism, cortical thickening of tubular bones, and transient hypocalcemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant Kenny-Caffey syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0012455", "names": ["9q-syndrome", "9Q- syndrome", "Kleefstra syndrome", "Kleefstra syndrome 1", "9q34 deletion syndrome", "9q34.3 microdeletion syndrome", "chromosome 9q deletion syndrome", "9Q subtelomeric deletion syndrome", "9q subtelomeric deletion syndrome", "chromosome 9Q34.3 deletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kleefstra syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0003612", "names": ["uterine ligament cancer", "cancer of uterine ligament", "tumor of the uterine Ligament", "uterine ligament neoplasm malignant", "malignant uterine ligament neoplasm", "Malignant Uterine Ligament Neoplasm", "malignant neoplasm of uterine ligament", "Malignant neoplasm of uterine ligament NOS", "malignant neoplasm of uterine ligament (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine ligament cancer", "shortest_name_length": 23}
{"curie": "UMLS:C4329972", "names": ["Factor XII Inactivation", "Factor XII Inhibitor Present"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Factor XII Inactivation", "shortest_name_length": 23}
{"curie": "UMLS:C1532533", "names": ["endophthalmitis fungal", "Fungal Endophthalmitis", "Fungal endophthalmitis", "Mycotic endophthalmitis", "Fungal endophthalmitis (disorder)", "Fungal endophthalmitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fungal endophthalmitis", "shortest_name_length": 22}
{"curie": "UMLS:C0037284", "names": ["skin lesion", "lesion skin", "Skin Lesion", "Skin lesion", "SKIN LESION", "lesions skin", "lesion; skin", "skin lesions", "skin; lesion", "Skin lesions", "skin lesions:", "skin lesion(s):", "Skin lesion NOS", "Skin lesion, NOS", "disorder lesions skin", "skin lesions (symptom)", "disorders lesions skin", "Skin lesion (disorder)", "skin lesions (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin lesion", "shortest_name_length": 11}
{"curie": "MONDO:0008991", "names": ["CLH SYNDROME", "Clh syndrome", "Verloove Vanhorick Brubakk syndrome", "Verloove Vanhorick-Brubakk syndrome", "Verloove-Vanhorick Brubakk syndrome", "Cleft-Limb-Heart Malformation Syndrome", "cleft-limb-heart malformation syndrome", "cleft limb heart malformation syndrome", "CLEFT-LIMB-HEART MALFORMATION SYNDROME", "Cleft Limb Heart Malformation Syndrome", "Verloove Vanhorick Brubakk syndrome (disorder)", "cleft-limb-heart malformation syndrome syndrome", "cleft lip-limb and heart malformations syndrome", "Cleft lip-limb and heart malformations syndrome", "Cleft lip, limb and heart malformation syndrome", "Verloove Vanhorick Brubakk syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Verloove Vanhorick-Brubakk syndrome", "shortest_name_length": 12}
{"curie": "UMLS:C0153871", "names": ["Plasmacytic Leukemia in Remission", "leukemia plasma cell in remission", "Plasma cell leukemia in remission", "plasma cell leukemia in remission", "Plasma Cell Leukemia in Remission", "Plasma cell leukemia, in remission", "Plasma cell leukaemia in remission", "Leukemia Plasmacytic (in Remission)", "Plasma cell leukaemia, in remission", "Leukemia plasmacytic (in remission)", "Plasmacytic Leukemia (in Remission)", "Leukaemia plasmacytic (in remission)", "Leukemia plasmacytic NOS (in remission)", "Leukaemia plasmacytic NOS (in remission)", "Plasma cell leukemia in remission (disorder)", "plasma cell leukemia in remission (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Plasma cell leukemia in remission", "shortest_name_length": 33}
{"curie": "UMLS:C2674009", "names": ["Microcornea, Rod-Cone Dystrophy, Cataract, And Posterior Staphyloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Microcornea, Rod-Cone Dystrophy, Cataract, And Posterior Staphyloma", "shortest_name_length": 67}
{"curie": "UMLS:C4525206", "names": ["Stage IV Hepatocellular Cancer", "Stage IV Liver Cell Carcinoma AJCC v8", "Stage IV Hepatocellular Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Hepatocellular Carcinoma AJCC v8", "shortest_name_length": 30}
{"curie": "UMLS:C0854574", "names": ["Twiddlers Syndrome", "Twiddler's syndrome", "Twiddler's Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Twiddler's syndrome", "shortest_name_length": 18}
{"curie": "UMLS:C1708750", "names": ["Low Grade Lung Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Grade Lung Neuroendocrine Neoplasm", "shortest_name_length": 38}
{"curie": "MONDO:0005829", "names": ["Louping Ill", "louping ill", "Louping ill", "Ill, Louping", "Louping ill (disorder)", "Ovine encephalomyelitis", "Louping ill encephalitis", "louping ill viral encephalitis", "encephalitis due to louping ill virus", "encephalitis due to louping ill virus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "louping ill", "shortest_name_length": 11}
{"curie": "UMLS:C4521718", "names": ["Stage IIIA Esophageal Adenocarcinoma", "Postneoadjuvant Therapy Stage IIIA Esophageal Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postneoadjuvant Therapy Stage IIIA Esophageal Adenocarcinoma AJCC v8", "shortest_name_length": 36}
{"curie": "MONDO:0003381", "names": ["Pituitary", "Dyspituitarism", "dyspituitarism", "Pituitary Disease", "disease pituitary", "pituitary disease", "PITUITARY DISEASE", "Pituitary disease", "pituitary disorder", "Pituitary Disorder", "Pituitary Diseases", "Pituitary disorder", "Disease, Pituitary", "pituitary diseases", "disorder pituitary", "Pituitary Disorders", "pituitary; disorder", "disorder; pituitary", "Pituitary disorders", "Diseases, Pituitary", "pituitary disorders", "Dyspituitarism, NOS", "Disorder, Pituitary", "disorders pituitary", "Hypophysis Disorders", "Disorders, Pituitary", "Hypophyseal Disorder", "Disorder, Hypophyseal", "Hypophyseal Disorders", "Disorder of pituitary", "Disorders, Hypophyseal", "Pituitary disorder NOS", "pituitary gland disease", "Pituitary Gland Disease", "Disease, Pituitary Gland", "Pituitary Gland Diseases", "pituitary gland disorder", "Pituitary Gland Disorder", "pituitary gland diseases", "Pituitary gland--Diseases", "Diseases, Pituitary Gland", "disorders gland pituitary", "disease of pituitary gland", "disorder of pituitary gland", "Disorder of pituitary gland", "GENERAL PITUITARY DISORDERS", "Disease of pituitary gland, NOS", "DISEASES OF THE PITUITARY GLAND", "Disorder of pituitary gland, NOS", "disease (or disorder); pituitary", "Abnormality of the pituitary gland", "pituitary gland disease or disorder", "Abnormality of the anterior pituitary", "Disorder of pituitary gland (disorder)", "disease or disorder of pituitary gland", "disorder of pituitary gland (diagnosis)", "Disorder of pituitary gland, unspecified", "Other and unspecified anterior pituitary hyperfunction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pituitary gland disorder", "shortest_name_length": 9}
{"curie": "MONDO:0005543", "names": ["cah", "CAH", "Type 1 AIH", "AIH type 1", "type 1 AIH", "chronic active hepatitis", "HEPATITIS CHRONIC ACTIVE", "Hepatitis chronic active", "hepatitis chronic active", "Chronic Active Hepatitis", "active chronic hepatitis", "Chronic active hepatitis", "Active chronic hepatitis", "Hepatitis, Chronic Active", "HEPATITIS, CHRONIC ACTIVE", "Hepatitis, chronic active", "chronic; hepatitis, active", "hepatitis; chronic, active", "autoimmune hepatitis type 1", "Autoimmune hepatitis type 1", "Type 1 Autoimmune Hepatitis", "Chronic aggressive hepatitis", "Autoimmune Hepatitis, Type 1", "HEPATITIS CHRONIC AGGRESSIVE", "Aggressive chronic hepatitis", "CAH - Chronic active hepatitis", "chronic active hepatitis (cah)", "CAH - Chronic aggressive hepatitis", "Chronic active hepatitis (disorder)", "chronic active hepatitis (diagnosis)", "Autoimmune hepatitis type 1 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune hepatitis type 1", "shortest_name_length": 3}
{"curie": "MONDO:0002569", "names": ["Dilated stomach", "dilated stomach", "dilation stomach", "gastric dilation", "stomach dilation", "Gastric Dilation", "dilation gastric", "Stomach Dilation", "STOMACH DISTENDED", "Dilation, Gastric", "Dilation, Stomach", "stomach distended", "Distended stomach", "distended stomach", "stomach dilatation", "Dilatation stomach", "dilatation stomach", "Gastric dilatation", "GASTRIC DILATATION", "DILATATION STOMACH", "gastric dilatation", "Gastric Dilatation", "STOMACH DILATATION", "Stomach dilatation", "Stomach Dilatation", "Dilatation, Gastric", "Dilatation, Stomach", "dilatation; stomach", "stomach; dilatation", "DILATION OF STOMACH", "Dilatation of stomach"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric dilatation", "shortest_name_length": 15}
{"curie": "UMLS:C0334598", "names": ["spongioneuroblastoma", "Spongioneuroblastoma", "spongioneuroblastoma (diagnosis)", "Spongioneuroblastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spongioneuroblastoma", "shortest_name_length": 20}
{"curie": "MONDO:0004286", "names": ["IPMN", "pancreatic IPMN", "Pancreatic IPMN", "IPMN, Pancreatic", "Pancreatic IPMNs", "IPMN of the pancreas", "Pancreatic Intraductal Neoplasms", "Intraductal papillary-mucinous adenoma", "intraductal papillary mucinous neoplasm", "Benign intra-ductal papillary mucinous neoplasm", "pancreatic intraductal papillary-mucinous tumor", "Pancreatic Intraductal Papillary-Mucinous Tumor", "Pancreatic Intraductal Papillary-Mucinous Neoplasm", "Pancreatic Intraductal Papillary Mucinous Neoplasm", "pancreatic intraductal papillary-mucinous neoplasm", "Intraductal papillary mucinous neoplasm of pancreas", "Intraductal Papillary-Mucinous Neoplasm, Pancreatic", "Intraductal Papillary Mucinous Neoplasm, Pancreatic", "intraductal papillary mucinous neoplasm of the pancreas", "Intraductal Papillary Mucinous Neoplasms of the Pancreas", "Intraductal papillary mucinous tumor with moderate dysplasia", "Intraductal papillary mucinous tumour with moderate dysplasia", "Intraductal papillary mucinous tumor with low grade dysplasia", "Intraductal papillary mucinous tumour with low grade dysplasia", "Intraductal papillary mucinous neoplasm of pancreas (disorder)", "Intraductal papillary mucinous neoplasm with moderate dysplasia", "Intraductal papillary mucinous tumor with intermediate dysplasia", "Intraductal papillary-mucinous adenoma (morphologic abnormality)", "Intraductal papillary mucinous neoplasm with low grade dysplasia", "Intraductal papillary mucinous tumour with intermediate dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic intraductal papillary-mucinous neoplasm", "shortest_name_length": 4}
{"curie": "UMLS:C2986702", "names": ["Stage IV Ovarian Low Malignant Potential Tumor", "stage IV ovarian low malignant potential tumor", "stage IV ovarian tumors of low malignant potential", "ovarian tumors of low malignant potential, stage IV", "stage IV borderline ovarian surface epithelial-stromal tumor", "Stage IV Borderline Ovarian Surface Epithelial-Stromal Tumor", "borderline ovarian surface epithelial-stromal tumor, stage IV"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Borderline Ovarian Surface Epithelial-Stromal Tumor", "shortest_name_length": 46}
{"curie": "MONDO:0010881", "names": ["Del(8)q(13)", "Monosomy 8q13", "monosomy 8q13", "Mesomelia synostoses", "mesomelia synostoses", "Verloes-David syndrome", "Verloes David syndrome", "8q13 microdeletion syndrome", "Mesomelia-synostoses syndrome", "mesomelia-synostoses syndrome", "MESOMELIA-SYNOSTOSES SYNDROME", "MESOMELIC DYSPLASIA, SYNDROMIC", "mesomelic dysplasia, syndromic", "CHROMOSOME 8q13 DELETION SYNDROME", "chromosome 8Q13 deletion syndrome", "8q13 microdeletion syndrome (disorder)", "Mesomelia synostoses syndrome Verloes David Pfeiffer type", "Mesomelia-synostoses syndrome, Verloes-David-Pfeiffer type", "mesomelia-synostoses syndrome, Verloes-David-Pfeiffer type", "Mesomelic dysplasia with acral synostoses Verloes David Pfeiffer type", "mesomelic dysplasia with acral synostoses, Verloes-David-Pfeiffer type", "Mesomelic dysplasia with acral synostoses, Verloes-David-Pfeiffer type", "MESOMELIC DYSPLASIA WITH ACRAL SYNOSTOSES, VERLOES-DAVID-PFEIFFER TYPE", "dominant mesomelic shortness of stature with acral synostoses, umbilical anomalies, and soft palate agenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mesomelia-synostoses syndrome", "shortest_name_length": 11}
{"curie": "UMLS:C1336330", "names": ["Stage II Uveal Melanoma", "Stage II Melanoma of Uvea", "Stage II Melanoma of the Uvea", "Stage II Uveal Melanoma AJCC v7", "Stage II Uveal Malignant Melanoma", "Stage II Malignant Melanoma of Uvea", "Stage II Malignant Melanoma of the Uvea"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Uveal Melanoma AJCC v7", "shortest_name_length": 23}
{"curie": "UMLS:C5237188", "names": ["Metastatic Pancreatic Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Pancreatic Neuroendocrine Neoplasm", "shortest_name_length": 45}
{"curie": "UMLS:C0343594", "names": ["Rodent-Borne Hemorrhagic Fever", "Rodent-borne hemorrhagic fever", "Rodent-borne haemorrhagic fever", "Rodent-borne hemorrhagic fever (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rodent-borne hemorrhagic fever", "shortest_name_length": 30}
{"curie": "MONDO:0023272", "names": ["goniodysgenesis intellectual disability short stature"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "goniodysgenesis intellectual disability short stature", "shortest_name_length": 53}
{"curie": "MONDO:0012721", "names": ["EPM3", "CLN14", "EPM 3", "PME type 3", "CLN14 disease", "progressive myoclonus epilepsy 3", "progressive myoclonic epilepsy 3", "neuronal ceroid lipofuscinosis 14", "Epilepsy, Progressive Myoclonic 3", "EPILEPSY, PROGRESSIVE MYOCLONIC 3", "CEROID LIPOFUSCINOSIS, NEURONAL, 14", "ceroid lipofuscinosis, neuronal, 14", "KCTD7 progressive myoclonic epilepsy", "epilepsy progressive myoclonic type 3", "progressive myoclonus epilepsy type 3", "Progressive myoclonus epilepsy type 3", "Progressive myoclonic epilepsy type 3", "progressive myoclonic epilepsy type 3", "progressive familial myoclonic epilepsy type 3", "Progressive myoclonic epilepsy type 3 (disorder)", "PME type 3 - progressive myoclonic epilepsy type 3", "Progressive myoclonic epilepsy due to KCTD7 deficiency", "progressive myoclonic epilepsy due to KCTD7 deficiency", "progressive myoclonic epilepsy caused by mutation in KCTD7", "progressive familial myoclonic epilepsy type 3 (diagnosis)", "epilepsy, progressive myoclonic 3, with or without intracellular inclusions", "epilepsy, progressive myoclonic, 3, with or without intracellular inclusions", "EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive myoclonic epilepsy type 3", "shortest_name_length": 4}
{"curie": "UMLS:C5667306", "names": ["Metastatic Appendix Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Appendix Adenocarcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0010748", "names": ["Tkc", "TKC", "TKCR", "Tkcr syndrome", "TKCR SYNDROME", "Goeminne syndrome", "GOEMINNE SYNDROME", "Goeminne TKCR syndrome", "Torticollis keloids cryptorchidism renal dysplasia", "torticollis keloids cryptorchidism renal dysplasia", "Torticollis, Keloids, Cryptorchidism, and Renal Dysplasia", "torticollis, keloids, cryptorchidism, and renal dysplasia", "TORTICOLLIS, KELOIDS, CRYPTORCHIDISM, AND RENAL DYSPLASIA", "torticollis-keloids-cryptorchidism-renal dysplasia syndrome", "TORTICOLLIS, KELOIDS, CRYPTORCHIDISM, AND RENAL DYSPLASIA (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "torticollis-keloids-cryptorchidism-renal dysplasia syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0022462", "names": ["anophthalmia esophageal atresia cryptorchidism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anophthalmia esophageal atresia cryptorchidism", "shortest_name_length": 46}
{"curie": "UMLS:C0599547", "names": ["radiation induced mosaicism", "Radiation-Induced Mosaicism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radiation-Induced Mosaicism", "shortest_name_length": 27}
{"curie": "MONDO:0012527", "names": ["Cpp4", "CPP4", "CTPP4", "CTRCT11", "posterior polar cataract 4", "cataract 11 multiple types", "CATARACT 11, MULTIPLE TYPES", "Posterior polar cataract, 4", "cataract 11, multiple types", "Cataract, posterior polar, 4", "cataract, posterior polar, 4", "CATARACT, POSTERIOR POLAR, 4", "PITX3 early-onset non-syndromic cataract", "cataract 11, syndromic, autosomal recessive", "early-onset non-syndromic cataract caused by mutation in PITX3", "cataract 11 with microphthalmia and neurodevelopmental abnormalities", "CATARACT 11 WITH MICROPHTHALMIA AND NEURODEVELOPMENTAL ABNORMALITIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 11 multiple types", "shortest_name_length": 4}
{"curie": "MONDO:0000374", "names": ["bile duct in situ carcinoma", "stage 0 bile duct carcinoma", "bile duct carcinoma in situ", "carcinoma in situ of bile duct"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bile duct carcinoma in situ", "shortest_name_length": 27}
{"curie": "MONDO:0030049", "names": ["SRXX5", "46,XX SEX REVERSAL 5", "46,xx sex reversal 5", "46,XX sex reversal 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,xx sex reversal 5", "shortest_name_length": 5}
{"curie": "MONDO:0016383", "names": ["diabete insipidus nephrogenic", "Diabetes insipidus nephrogenic", "Nephrogenic Diabetes Insipidus", "DIABETES INSIPIDUS NEPHROGENIC", "Nephrogenic diabetes insipidus", "nephrogenic diabetes insipidus", "diabetes insipidus nephrogenic", "nephrogenic; diabetes insipidus", "DIABETES INSIPIDUS, NEPHROGENIC", "Diabetes Insipidus, Nephrogenic", "diabetes; insipidus, nephrogenic", "ADH resistant diabetes insipidus", "Nephrogenic diabetes insipidus, NOS", "NDI - Nephrogenic diabetes insipidus", "diabetes insipidus nephrogenic type 1", "diabetes insipidus nephrogenic X-linked", "vasopressin-resistant diabetes insipidus", "Nephrogenic diabetes insipidus (disorder)", "nephrogenic diabetes insipidus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrogenic diabetes insipidus", "shortest_name_length": 29}
{"curie": "UMLS:C5420053", "names": ["Sinonasal Desmoid Fibromatosis", "Sinonasal Desmoid-Type Fibromatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Desmoid Fibromatosis", "shortest_name_length": 30}
{"curie": "UMLS:C3640021", "names": ["Bilateral Anophthalmos", "Bilateral anophthalmos", "Anophthalmos, Bilateral", "Anophthalmos of both eyes", "Bilateral anophthalmos of eyes", "Anophthalmos of bilateral eyes", "Anophthalmos of bilateral eyes (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bilateral anophthalmos of eyes", "shortest_name_length": 22}
{"curie": "MONDO:0011362", "names": ["MPRM", "MFM9", "HMERF", "ADMERF", "HIBM-ERF", "HMERF-ERF", "MFM-titinopathy", "Edstrom Myopathy", "EDSTROM MYOPATHY", "Edström myopathy", "Edstrom myopathy", "Edström Myopathy", "myofibrillar myopathy 9", "Myofibrillar myopathy-titinopathy", "Hereditary Myopathy with Early Respiratory Failure", "HEREDITARY MYOPATHY WITH EARLY RESPIRATORY FAILURE", "hereditary myopathy with early respiratory failure", "Hereditary myopathy with early respiratory failure", "myofibrillar myopathy with early respiratory failure", "Myofibrillar myopathy with early respiratory failure", "myofibrillar myopathy 9 with early respiratory failure", "distal myopathy with early respiratory muscle involvement", "myopathy, myofibrillar, 9, with early respiratory failure", "MYOPATHY, MYOFIBRILLAR, 9, WITH EARLY RESPIRATORY FAILURE", "HMERF - hereditary myopathy with early respiratory failure", "hereditary proximal myopathy with early respiratory failure", "Hereditary proximal myopathy with early respiratory failure", "proximal myopathy with early respiratory muscle involvement", "MYOPATHY, PROXIMAL, WITH EARLY RESPIRATORY MUSCLE INVOLVEMENT", "Myopathy, Proximal, with Early Respiratory Muscle Involvement", "Hereditary myopathy with early respiratory failure (disorder)", "myopathy, proximal, with early respiratory muscle involvement", "hereditary inclusion body myopathy with early respiratory failure", "autosomal dominant distal myopathy with early respiratory failure", "Hereditary inclusion body myopathy with early respiratory failure", "myopathy, distal, with early respiratory failure, autosomal dominant", "Myopathy, Distal, With Early Respiratory Failure, Autosomal Dominant", "MPRM - myopathy, proximal, with early respiratory muscle involvement", "MYOPATHY, DISTAL, WITH EARLY RESPIRATORY FAILURE, AUTOSOMAL DOMINANT", "distal myopathy with early respiratory muscle involvement (diagnosis)", "[OBSOLETE] Myopathy, Distal, With Early Respiratory Failure, Autosomal Dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy, myofibrillar, 9, with early respiratory failure", "shortest_name_length": 4}
{"curie": "UMLS:C5669863", "names": ["Locally Advanced Paranasal Sinus Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Paranasal Sinus Squamous Cell Carcinoma", "shortest_name_length": 56}
{"curie": "UMLS:C1710250", "names": ["Superior and Inferior Paraaortic Paraganglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Superior and Inferior Paraaortic Paraganglioma", "shortest_name_length": 46}
{"curie": "UMLS:C0751194", "names": ["Spinal Subdural Hematoma", "Spinal subdural hematoma", "Hematoma, Spinal Subdural", "Spinal subdural haematoma", "Subdural Hematoma, Spinal", "Spinal Subdural Hematomas", "Hematoma, Subdural, Spinal", "Subdural Hematomas, Spinal", "Hematomas, Spinal Subdural", "Spinal subdural hematoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hematoma, Subdural, Spinal", "shortest_name_length": 24}
{"curie": "UMLS:C4763852", "names": ["Acute Hepatitis E", "Acute Hepatitis E Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Hepatitis E Infection", "shortest_name_length": 17}
{"curie": "UMLS:C0856171", "names": ["Coronary artery disease aggravated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Coronary artery disease aggravated", "shortest_name_length": 34}
{"curie": "UMLS:C1333451", "names": ["High-Grade Esophageal Squamous Dysplasia", "High Grade Esophageal Squamous Intraepithelial Neoplasia", "High-Grade Esophageal Squamous Intraepithelial Neoplasia", "Esophageal High-Grade Squamous Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Esophageal Squamous Intraepithelial Neoplasia", "shortest_name_length": 40}
{"curie": "MONDO:0006466", "names": ["SETTLE", "settle", "settles", "settle tumor", "SETTLE tumor", "SETTLE tumour", "Spindle epithelial tumor with thymus-like element", "spindle epithelial tumor with thymus-like element", "Spindle Epithelial Tumor with Thymus-Like Elements", "Spindle epithelial tumour with thymus-like element", "Spindle epithelial tumor with thymus-like differentiation", "Spindle epithelial tumour with thymus-like differentiation", "spindle epithelial tumor with thymus-like element (diagnosis)", "spindle epithelial tumor with thymus-like differentiation tumor", "Thyroid Gland Spindle Epithelial Tumor with Thymus-Like Elements", "Thyroid Gland Spindle Cell Tumor with Thymus-Like Differentiation", "thyroid gland spindle cell tumor with thymus-like differentiation", "spindle epithelial tumour with thymus-like differentiation tumour", "Spindle epithelial tumor with thymus-like element (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid gland spindle cell tumor with thymus-like differentiation", "shortest_name_length": 6}
{"curie": "UMLS:C5556692", "names": ["Adult Myofibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Myofibroma", "shortest_name_length": 16}
{"curie": "MONDO:0006744", "names": ["cochlear hydrops", "Cochlear hydrops", "HYDROPS, COCHLEAR", "labyrinthine hydrops", "Labyrinthine hydrops", "Endolymphatic Hydrops", "Endolymphatic hydrops", "HYDROPS, LABYRINTHINE", "endolymphatic hydrops", "HYDROPS, ENDOLYMPHATIC", "Hydrops, Endolymphatic", "endolymphatic; hydrops", "hydrops; endolymphatic", "Cochlear hydrops (disorder)", "cochlear hydrops (diagnosis)", "Endolymphatic hydrops syndrome", "Labyrinthine hydrops (disorder)", "Endolymphatic hydrops (disorder)", "labyrinthine hydrops (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endolymphatic hydrops", "shortest_name_length": 16}
{"curie": "MONDO:0002304", "names": ["Protein S Deficiency", "protein s deficiency", "s protein deficiency", "deficiency protein s", "Protein S deficiency", "protein S deficiency", "Deficiency, Protein S", "Protein S Deficiencies", "protein s deficiencies", "Deficiencies, Protein S", "Reduced protein S activity", "Protein S Deficiency Disease", "Protein S deficiency disease", "protein S deficiency (diagnosis)", "Protein S deficiency disease (disorder)", "Hereditary Thrombophilia Due To Protein S Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "protein S deficiency", "shortest_name_length": 20}
{"curie": "MONDO:0015126", "names": ["polyendocrinopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyendocrinopathy", "shortest_name_length": 18}
{"curie": "MONDO:0010503", "names": ["BARTS5", "Bartter disease type 5", "MAGED2 Bartter syndrome", "Bartter syndrome caused by mutation in MAGED2", "Bartter syndrome, type 5, antenatal, transient", "BARTTER SYNDROME, TYPE 5, ANTENATAL, TRANSIENT", "Bartter syndrome, type 5, antenatal, transient, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bartter disease type 5", "shortest_name_length": 6}
{"curie": "UMLS:C1335710", "names": ["Relapsed MPNST", "Recurrent MPNST", "Relapsed Malignant Peripheral Nerve Sheath Tumor", "Recurrent Malignant Peripheral Nerve Sheath Tumor", "Relapsed Malignant Peripheral Nerve Sheath Neoplasm", "Recurrent Malignant Peripheral Nerve Sheath Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Malignant Peripheral Nerve Sheath Tumor", "shortest_name_length": 14}
{"curie": "MONDO:0001412", "names": ["Conjunctival concretion", "conjunctival concretion", "concretion; conjunctiva", "conjunctiva; concretion", "Conjunctival concretions", "conjunctival concretions", "Conjunctival concretion, NOS", "Conjunctival concretion (disorder)", "conjunctival concretions (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "conjunctival concretion", "shortest_name_length": 23}
{"curie": "MONDO:0021366", "names": ["middle ear tumor", "ear middle tumor", "Middle ear tumor", "middle Ear tumor", "Middle Ear Tumor", "Middle ear tumour", "ear middle tumors", "ear middle tumour", "Tumor of middle ear", "middle Ear neoplasm", "Middle Ear Neoplasm", "Middle ear neoplasm", "middle ear neoplasm", "Tumor of Middle Ear", "tumor of middle ear", "tumor of middle Ear", "Tumour of middle ear", "Neoplasm of Middle Ear", "neoplasm of middle ear", "Neoplasm of middle ear", "tumor of the middle Ear", "Tumor of the Middle Ear", "Neoplasm of the middle ear", "neoplasm of the middle Ear", "Neoplasm of the Middle Ear", "Neoplasia of the middle ear", "middle ear neoplasm (disease)", "auditory neoplasm of middle ear", "Neoplasm of middle ear (disorder)", "neoplasm of middle ear (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplasm of middle ear", "shortest_name_length": 16}
{"curie": "MONDO:0018981", "names": ["BINS", "benign idiopathic neonatal seizures", "benign nonfamilial neonatal seizures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign idiopathic neonatal seizures", "shortest_name_length": 4}
{"curie": "UMLS:C3897648", "names": ["Secondary Central Nervous System Non-Hodgkin Lymphoma", "secondary central nervous system non-Hodgkin lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary Central Nervous System Non-Hodgkin Lymphoma", "shortest_name_length": 53}
{"curie": "MONDO:0001073", "names": ["idiopathic progressive polyneuropathy", "POLYNEUROPATHY IDIOPATHIC PROGRESSIVE", "Polyneuropathy idiopathic progressive", "Idiopathic progressive polyneuropathy", "polyneuropathy; idiopathic progressive", "idiopathic progressive; polyneuropathy", "Idiopathic progressive polyneuropathy (disorder)", "idiopathic progressive polyneuropathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic progressive polyneuropathy", "shortest_name_length": 37}
{"curie": "MONDO:0060456", "names": ["CEREBRAL SCLEROSIS, DIFFUSE, SCHOLZ TYPE", "Cerebral Sclerosis, Diffuse, Scholz Type", "cerebral sclerosis, diffuse, scholz type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral sclerosis, diffuse, scholz type", "shortest_name_length": 40}
{"curie": "UMLS:C5444799", "names": ["Cutaneous AVM/H", "Cirsoid Aneurysm", "Acral Arteriovenous Tumor", "Cutaneous Arteriovenous Malformation", "Cutaneous Arteriovenous Malformation/Hemangioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous Arteriovenous Malformation/Hemangioma", "shortest_name_length": 15}
{"curie": "UMLS:C1336396", "names": ["Stage IVC Larynx Verrucous Carcinoma", "Stage IVC Laryngeal Verrucous Carcinoma", "Stage IVC Verrucous Carcinoma of Larynx", "Stage IVC Verrucous Carcinoma of the Larynx", "Stage IVC Laryngeal Throat Verrucous Cancer", "Stage IVC Laryngeal Verrucous Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Laryngeal Verrucous Carcinoma AJCC v7", "shortest_name_length": 36}
{"curie": "MONDO:0017893", "names": ["familial AML", "Familial AML", "inherited AML", "Inherited AML", "Pure familial AML", "inherited acute myeloid leukemia", "Inherited acute myeloid leukemia", "Inherited acute myeloid leukaemia", "hereditary acute myeloid leukemia", "Pure familial acute myeloid leukemia", "Pure familial acute myeloid leukaemia", "Inherited acute myeloid leukemia (disorder)", "Inherited acute myeloid leukemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited acute myeloid leukemia", "shortest_name_length": 12}
{"curie": "UMLS:C4521805", "names": ["Stage IIIB Anal Cancer", "Stage IIIB Anal Cancer AJCC v8", "Stage IIIB Anal Carcinoma AJCC v8", "Stage IIIB Anal Canal and Perianal (Anal Margin) Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Anal Cancer AJCC v8", "shortest_name_length": 22}
{"curie": "UMLS:C4330048", "names": ["GCK-Associated Hyperinsulinism", "Glucokinase-Associated Hyperinsulinism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Glucokinase-Associated Hyperinsulinism", "shortest_name_length": 30}
{"curie": "MONDO:0010343", "names": ["ASPGX2", "Asperger syndrome susceptibility, X-linked 2", "susceptibility to X-linked asperger syndrome 2", "Asperger syndrome, X-linked, susceptibility to, 2", "ASPERGER syndrome, X-linked, susceptibility to, 2", "Asperger syndrome, X-linked, susceptibility to, type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Asperger syndrome, X-linked, susceptibility to, 2", "shortest_name_length": 6}
{"curie": "MONDO:0007192", "names": ["AABT", "taurine renal reabsorption", "TAURINE RENAL REABSORPTION", "BETA-amino acids, renal TRANSPORT OF", "beta-amino acids, renal transport of", "BETA-AMINO ACIDS, RENAL TRANSPORT OF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "beta-amino acids, renal transport of", "shortest_name_length": 4}
{"curie": "MONDO:0018782", "names": ["type 1 interferonopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type 1 interferonopathy", "shortest_name_length": 23}
{"curie": "MONDO:0006450", "names": ["TMN", "therapy-related AML and MDS", "Therapy-Related AML and MDS", "Therapy related myeloid neoplasm", "Therapy-Related Myeloid Neoplasm", "therapy-related myeloid neoplasm", "Therapy-related Myeloid Neoplasms", "therapy-related myeloid neoplasms", "Therapy-Related Acute Myeloid Leukemia and Myelodysplastic Syndrome", "therapy-related acute myeloid leukemia and myelodysplastic syndrome", "Acute Myeloid Leukaemias and Myelodysplastic Syndromes, Therapy-Related", "acute myeloid Leukaemias and myelodysplastic syndromes, therapy-related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "therapy-related myeloid neoplasm", "shortest_name_length": 3}
{"curie": "UMLS:C0270328", "names": ["Daytime wetting", "Daytime Wetting", "Diurnal enuresis", "Diurnal Enuresis", "enuresis diurnal", "Daytime enuresis", "Wetting, Daytime", "Enuresis, Diurnal", "Daytime enuresis (finding)", "Daytime Urinary Incontinence", "daytime urinary incontinence", "Diurnal enuresis (diagnosis)", "Incontinence, Daytime Urinary", "Urinary Incontinence, Daytime", "unable to restrain urination during day", "unable to restrain urination during day (symptom)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diurnal Enuresis", "shortest_name_length": 15}
{"curie": "MONDO:0013952", "names": ["CGK", "PBD13A", "peroxisome biogenesis disorder 13A", "peroxisome biogenesis disorder 13A (Zellweger)", "PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER)", "PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP K", "peroxisome biogenesis disorder, complementation group K", "Peroxisome Biogenesis Disorder, Complementation Group K"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder 13A (Zellweger)", "shortest_name_length": 3}
{"curie": "UMLS:C0334600", "names": ["Differentiated Retinoblastoma", "differentiated retinoblastoma", "retinoblastoma; differentiated", "Retinoblastoma, differentiated", "differentiated; retinoblastoma", "Retinoblastoma - differentiated", "differentiated retinoblastoma (diagnosis)", "Retinoblastoma, differentiated (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retinoblastoma, differentiated", "shortest_name_length": 29}
{"curie": "MONDO:0016797", "names": ["multiple mtDNA deletion syndrome", "multiple mitochondrial DNA deletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple mitochondrial DNA deletion syndrome", "shortest_name_length": 32}
{"curie": "UMLS:C4761514", "names": ["Recurrent Giant Cell Glioblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Giant Cell Glioblastoma", "shortest_name_length": 33}
{"curie": "MONDO:0002254", "names": ["syndrome", "Syndrome", "Syndromes", "syndromes", "Syndrome, NOS", "symptom cluster", "Symptom Cluster", "Cluster, Symptom", "cluster, symptom", "symptom clusters", "Symptom Clusters", "clusters, symptom", "syndromic disease", "Clusters, Symptom", "syndromic disease or disorder", "syndrome associated with disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic disease", "shortest_name_length": 8}
{"curie": "MONDO:0001954", "names": ["Trousseau's syndrome", "Thrombophlebitis migrans", "Thrombophlebitis Migrans", "thrombophlebitis migrans", "thrombophlebitis; migrans", "migrans; thrombophlebitis", "Migratory thrombophlebitis", "migrating thrombophlebitis", "migratory thrombophlebitis", "THROMBOPHLEBITIS MIGRATORY", "Thrombophlebitis, migrating", "THROMBOPHLEBITIS, MIGRATORY", "Trousseau's syndrome (diagnosis)", "Thrombophlebitis migrans (disorder)", "thrombophlebitis migrans (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombophlebitis migrans", "shortest_name_length": 20}
{"curie": "UMLS:C4054726", "names": ["Infant Leukemia", "Leukemia in Infancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infant Leukemia", "shortest_name_length": 15}
{"curie": "UMLS:C1333594", "names": ["Fallopian Tube Non-Neoplastic Disease", "Fallopian Tube Non-Neoplastic Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fallopian Tube Non-Neoplastic Disorder", "shortest_name_length": 37}
{"curie": "UMLS:C4524713", "names": ["Clinical Stage II Gastroesophageal Junction Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage II Gastroesophageal Junction Adenocarcinoma AJCC v8", "shortest_name_length": 66}
{"curie": "MONDO:0020317", "names": ["AML with 11q23 abnormalities", "AML with t(9;11)(p22;q33);MLLT3-MLL", "AML with t(9;11)(p22;q23); MLLT3-MLL", "AML with t(9;11)(p21.3;q23.3); KMT2A-MLLT3", "acute myeloid leukemia with MLL abnormalities", "acute myeloid leukemia with 11q23 abnormalities", "acute myeloid leukemia with 11q23 (MLL) abnormalities", "acute myeloid leukemia with t(9:11)(p22;q23);MLLT3-MLL", "Acute Myeloid Leukemia with t(9;11)(p22;q23); MLLT3-MLL", "acute myeloid leukemia with t(9;11)(p22;q23); MLLT3-MLL", "Acute myeloid leukemia with t(9;11)(p22;q23); MLLT3-MLL", "Acute myeloid leukemia with t(9:11)(p22;q23); MLLT3-MLL", "Acute myeloid leukaemia with t(9:11)(p22;q23); MLLT3-MLL", "Acute myeloid leukaemia with t(9;11)(p22;q23); MLLT3-MLL", "Acute Myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3-MLL", "acute myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3-KMT2A", "Acute Myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3-KMT2A", "acute myeloid leukemia with t(9;11)(p22.3;q23.3); MLLT3-KMT2A", "Acute Myeloid Leukemia with t(9;11)(p22.3;q23.3); MLLT3-KMT2A", "acute myeloid leukemia with t(9:11)(p22;q23);MLLT3-MLL (diagnosis)", "Acute myeloid leukemia with t(9:11)(p22;q23); MLLT3-MLL (disorder)", "Acute Myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3 (AF9)-KMT2A", "Acute myeloid leukemia with t(9;11)(p22;q23); MLLT3-MLL (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia with 11q23 abnormalities", "shortest_name_length": 28}
{"curie": "MONDO:0002209", "names": ["HEELSPUR", "heelspur", "HEEL SPUR", "heel spur", "Heel Spur", "heelspurs", "Heel Spurs", "heel spurs", "Spur, Heel", "Spurs, Heel", "calcaneal spur", "calcaneus spur", "Calcaneal Spur", "CALCANEUS SPUR", "Calcaneal spur", "spur; calcaneal", "calcaneal spurs", "calcaneus spurs", "Spur, Calcaneal", "Calcaneal Spurs", "calcaneal; spur", "Spurs, Calcaneal", "calcaneal spurring", "calcaneus exostosis", "Calcaneal spur (finding)", "calcaneal spur (diagnosis)", "Calcaneal spur, unspecified foot"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heel spur", "shortest_name_length": 8}
{"curie": "MONDO:0020714", "names": ["MEOAL", "mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy", "MITOCHONDRIAL MYOPATHY, EPISODIC, WITH OR WITHOUT OPTIC ATROPHY AND REVERSIBLE LEUKOENCEPHALOPATHY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy", "shortest_name_length": 5}
{"curie": "UMLS:C2987188", "names": ["Pancreatic Intraductal Neoplasm", "Pancreatic Intraductal Neoplasms", "Neoplasm, Pancreatic Intraductal", "Intraductal Neoplasm, Pancreatic", "Intraductal Neoplasms, Pancreatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Intraductal Neoplasms", "shortest_name_length": 31}
{"curie": "MONDO:0032805", "names": ["HOD", "hypopigmentation, organomegaly, and delayed myelination and development", "HYPOPIGMENTATION, ORGANOMEGALY, AND DELAYED MYELINATION AND DEVELOPMENT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypopigmentation, organomegaly, and delayed myelination and development", "shortest_name_length": 3}
{"curie": "MONDO:0017476", "names": ["upper limb hypertrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "upper limb hypertrophy", "shortest_name_length": 22}
{"curie": "MONDO:0003292", "names": ["Anal Leiomyoma", "anal leiomyoma", "anus leiomyoma", "leiomyoma of anus", "Leiomyoma of Anus", "Leiomyoma of the Anus", "leiomyoma of the anus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anus leiomyoma", "shortest_name_length": 14}
{"curie": "MONDO:0008244", "names": ["PBT", "piebaldism", "Piebaldism", "PIEBALDISM", "piebald trait", "PIEBALD TRAIT", "Piebald Trait", "partial albinism", "Partial Albinism", "Partial albinism", "Albinism, Partial", "Cutaneous Albinism", "Cutaneous albinism", "Albinism, Cutaneous", "Piebaldism (disorder)", "Partial albinism (disorder)", "Albinism, partial, cutaneous", "Congenital partial leucoderma", "Partial absent skin pigmentation", "Congenital partial albinism on face, trunk, or limbs", "Congenital partial albinism (leukoderma) on face, trunk, or limbs"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "piebaldism", "shortest_name_length": 3}
{"curie": "UMLS:C0234527", "names": ["motor apraxia", "Apractognosia", "Motor apraxia", "Motor Apraxia", "Motor Apraxias", "motor apraxias", "Apraxia, Motor", "Apraxias, Motor", "Cortical apraxia", "Innervation apraxia", "constructional apraxia", "Constructional apraxia", "Motor apraxia (finding)", "motor apraxia was noted", "Constructional dyspraxia", "constructional dyspraxia", "Constructional apraxia (finding)", "motor apraxia (physical finding)", "constructional apraxia was noted", "constructional apraxia (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Apraxia, Motor", "shortest_name_length": 13}
{"curie": "MONDO:0004799", "names": ["Palpebral ulcer", "ulcerative blepharitis", "Ulcerative blepharitis", "BLEPHARITIS, ULCERATIVE", "Ulcerative blepharitis (disorder)", "ulcerative blepharitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ulcerative blepharitis", "shortest_name_length": 15}
{"curie": "UMLS:C0033943", "names": ["Traumatic Psychoses", "Traumatic Psychosis", "Traumatic psychoses", "Psychoses, Traumatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Psychoses, Traumatic", "shortest_name_length": 19}
{"curie": "MONDO:0004551", "names": ["Meckel diverticulitis", "Meckel Diverticulitis", "Diverticulitis Meckel's", "Meckel's diverticulitis", "Meckel's Diverticulitis", "Meckel's diverticulum inflammation", "Meckel's diverticulitis (disorder)", "Meckel's diverticulitis (diagnosis)", "inflammation of Meckel's diverticulum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meckel diverticulitis", "shortest_name_length": 21}
{"curie": "MONDO:0011807", "names": ["SLEH1", "systemic lupus erythematosus with hemolytic anemia", "systemic lupus erythematosus, hemolytic Anemia-related", "SYSTEMIC LUPUS ERYTHEMATOSUS, HEMOLYTIC ANEMIA-RELATED", "systemic lupus erythematosus with hemolytic anemia, susceptibility to, 1", "SYSTEMIC LUPUS ERYTHEMATOSUS WITH HEMOLYTIC ANEMIA, SUSCEPTIBILITY TO, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "systemic lupus erythematosus with hemolytic anemia, susceptibility to, 1", "shortest_name_length": 5}
{"curie": "UMLS:C5207986", "names": ["Immune-mediated myocarditis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immune-mediated myocarditis", "shortest_name_length": 27}
{"curie": "MONDO:0004428", "names": ["alveoli adenoma", "Alveolar adenoma", "alveolar adenoma", "Alveolar Adenoma", "adenoma; alveolar", "alveolar; adenoma", "Adenoma of Alveoli", "adenoma of alveoli", "Adenoma of the Alveoli", "adenoma of the alveoli", "ADENOMA, BRONCHIOLOALVEOLAR, BENIGN", "adenoma, bronchioloalveolar, benign", "alveolar adenoma (morphologic abnormality)", "Alveolar adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alveoli adenoma", "shortest_name_length": 15}
{"curie": "UMLS:C5554988", "names": ["Unresectable Myxofibrosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Myxofibrosarcoma", "shortest_name_length": 29}
{"curie": "MONDO:0014819", "names": ["DRS3", "DVL3 Robinow syndrome", "autosomal dominant Robinow syndrome 3", "Robinow syndrome, autosomal dominant 3", "ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3", "autosomal dominant Robinow syndrome type 3", "Robinow syndrome, autosomal dominant type 3", "Robinow syndrome caused by mutation in DVL3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant Robinow syndrome 3", "shortest_name_length": 4}
{"curie": "MONDO:0007900", "names": ["NDNC3", "PORCELAIN NAILS", "porcelain nails", "leukonychia Striatus", "Leukonychia punctata", "LEUKONYCHIA STRIATUS", "LEUKONYCHIA PUNCTATA", "Leuconychia punctata", "leukonychia punctata", "leukonychia punctata was seen", "Leukonychia punctata (disorder)", "Gorlin Bushkell Jensen syndrome", "leukonychia totalis and/or partialis", "LEUKONYCHIA TOTALIS AND/OR PARTIALIS", "PLCD1 inherited isolated nail anomaly", "nonsyndromic congenital nail disorder 3", "leukonychia punctata (physical finding)", "NAIL DISORDER, NONSYNDROMIC CONGENITAL, 3", "nail disorder, nonsyndromic congenital, 3", "nonsyndromic congenital nail disorder type 3", "nail disorder, nonsyndromic congenital, type 3", "nails discoloration white (leukonychia) punctata", "nail disorder, nonsyndromic congenital, 3, (leukonychia)", "leukonychia totalis multiple sebaceous cysts renal calculi", "inherited isolated nail anomaly caused by mutation in PLCD1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nonsyndromic congenital nail disorder 3", "shortest_name_length": 5}
{"curie": "MONDO:0010367", "names": ["ISS", "SHOX-related short stature", "idiopathic familial short stature", "short stature, idiopathic familial", "short stature, idiopathic, X-linked", "SHORT STATURE, IDIOPATHIC, X-LINKED", "Short Stature, Idiopathic, X-Linked", "Short stature homeobox related short stature", "SHOX (short stature homeobox) related short stature", "Short stature homeobox related short stature (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SHOX-related short stature", "shortest_name_length": 3}
{"curie": "MONDO:0010825", "names": ["Houlston-Ironton-Temple syndrome", "atrioventricular defect-blepharophimosis-radial and anal defect syndrome", "ATRIOVENTRICULAR SEPTAL DEFECT WITH BLEPHAROPHIMOSIS AND ANAL AND RADIAL DEFECTS", "atrioventricular septal defect with blepharophimosis and anal and radial defects", "Atrioventricular Septal Defect with Blepharophimosis and Anal and Radial Defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrioventricular defect-blepharophimosis-radial and anal defect syndrome", "shortest_name_length": 32}
{"curie": "MONDO:0010424", "names": ["SMDP4", "Csf2Ra deficiency", "CSF2RA DEFICIENCY", "CSF2RA Deficiency", "PAP due to CSF2RA Deficiency", "Pap due to Csf2Ra deficiency", "PAP DUE TO CSF2RA DEFICIENCY", "pulmonary alveolar proteinosis, congenital, 4", "Pulmonary Alveolar Proteinosis, Congenital, 4", "PULMONARY ALVEOLAR PROTEINOSIS, CONGENITAL, 4", "SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 4", "surfactant metabolism dysfunction, pulmonary, 4", "Surfactant Metabolism Dysfunction, Pulmonary, 4", "surfactant metabolism dysfunction, pulmonary, type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "surfactant metabolism dysfunction, pulmonary, 4", "shortest_name_length": 5}
{"curie": "UMLS:C0855178", "names": ["Stage III Bladder Adenocarcinoma", "Bladder adenocarcinoma stage III", "Stage III Bladder Adenocarcinoma AJCC v7", "Stage III Bladder Adenocarcinoma AJCC v6", "Stage III Bladder Adenocarcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder adenocarcinoma stage III", "shortest_name_length": 32}
{"curie": "UMLS:C0276340", "names": ["Respiratory syncytial virus bronchiolitis", "bronchiolitis; respiratory syncytial virus", "respiratory syncytial virus; bronchiolitis", "Respiratory syncytial virus bronchiolitis (disorder)", "bronchiolitis infectious respiratory syncytial virus", "Respiratory syncytial virus bronchiolitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Respiratory syncytial virus bronchiolitis", "shortest_name_length": 41}
{"curie": "MONDO:0017812", "names": ["segmental progressive overgrowth syndrome with fibroadipose hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "segmental progressive overgrowth syndrome with fibroadipose hyperplasia", "shortest_name_length": 71}
{"curie": "MONDO:0013336", "names": ["Del(19)(p13.13)", "monosomy 19p13.13", "Monosomy 19p13.13", "19p13.13 microdeletion syndrome", "Chromosome 19p13.13 deletion syndrome", "chromosome 19p13.13 deletion syndrome", "CHROMOSOME 19p13.13 DELETION SYNDROME", "CHROMOSOME 19p13.13 DUPLICATION SYNDROME", "chromosome 19P13.13 Duplication syndrome", "19p13.13 microdeletion syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 19p13.13 deletion syndrome", "shortest_name_length": 15}
{"curie": "UMLS:C3887590", "names": ["ureter stenosis", "stenosis ureters", "stricture ureter", "URETER STRICTURE", "ureter stricture", "ureter; stricture", "ureteric stenosis", "ureter; narrowing", "ureteral stenosis", "stricture; ureter", "URETER, STRICTURE", "strictures ureter", "narrowing; ureter", "ureteral stricture", "Ureteral stricture", "stricture ureteral", "Ureteral Stricture", "stricture of ureter", "Stricture of ureter", "strictures ureteral", "Stricture of ureter (disorder)", "stricture of ureter (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stricture of ureter", "shortest_name_length": 15}
{"curie": "MONDO:0005527", "names": ["neurotoxicity", "NEUROTOXICITY", "Neurotoxicity", "Neurotoxicosis", "Neurotoxicity NOS", "NEUROTIC TOXICITY", "Neurotoxic effect", "effects neurotoxic", "Neurotoxin Disease", "Neurotoxicity, NOS", "Neurotoxin Disorder", "Neurotoxin Diseases", "Neurotoxic Disorder", "Neurotoxin Disorders", "encephalopathy toxic", "Neurotoxic Disorders", "Toxic encephalopathy", "Toxic Encephalopathy", "ENCEPHALOPATHY TOXIC", "Encephalopathy toxic", "toxic encephalopathy", "Encephalopathy, Toxic", "ENCEPHALOPATHY, TOXIC", "toxic; encephalopathy", "encephalopathy; toxic", "Toxic Encephalopathies", "Neurotoxicity syndrome", "Neurotoxicity Syndrome", "neurotoxicity syndrome", "Encephalopathies, Toxic", "Neurotoxicity Syndromes", "Syndrome, Neurotoxicity", "neurotoxicity syndromes", "Nervous System Poisoning", "Syndromes, Neurotoxicity", "Neurotoxicity (disorder)", "Poisoning of nerve tissue", "Nervous System Poisonings", "Poisoning, Nervous System", "Poisonings, Nervous System", "Toxic induced encephalopathy", "toxic induced encephalopathy", "Toxic encephalopathy (disorder)", "toxic encephalopathy (diagnosis)", "Toxic disease or syndrome of nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "toxic encephalopathy", "shortest_name_length": 13}
{"curie": "UMLS:C3272799", "names": ["MP/HP", "Colorectal MP/HP", "Colorectal Mucin Poor Hyperplastic Polyp"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Mucin Poor Hyperplastic Polyp", "shortest_name_length": 5}
{"curie": "UMLS:C4526900", "names": ["Stage I Soft Tissue Sarcoma of the Trunk and Extremities", "Stage I Soft Tissue Sarcoma of the Trunk and Extremities AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Soft Tissue Sarcoma of the Trunk and Extremities AJCC v8", "shortest_name_length": 56}
{"curie": "UMLS:C3272856", "names": ["Anal MANEC", "Anal Canal MANEC", "Anal Mixed Adenoneuroendocrine Carcinoma", "Anal Canal Mixed Adenoneuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anal Canal Mixed Adenoneuroendocrine Carcinoma", "shortest_name_length": 10}
{"curie": "MONDO:0012595", "names": ["LPRS4", "LTA leprosy", "susceptibility to leprosy 4", "leprosy, susceptibility to, 4", "LEPROSY, SUSCEPTIBILITY TO, 4", "leprosy caused by mutation in LTA", "leprosy, susceptibility to, type 4", "LEPROSY, EARLY-ONSET, SUSCEPTIBILITY TO", "leprosy, early-onset, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leprosy, susceptibility to, 4", "shortest_name_length": 5}
{"curie": "UMLS:C5556716", "names": ["Advanced Vaginal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Vaginal Adenocarcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C5205939", "names": ["Prostate Paraganglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Paraganglioma", "shortest_name_length": 22}
{"curie": "UMLS:C5421209", "names": ["Recurrent Transformed Marginal Zone Lymphoma to Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Transformed Marginal Zone Lymphoma to Diffuse Large B-Cell Lymphoma", "shortest_name_length": 77}
{"curie": "MONDO:0003732", "names": ["adult central nervous system mature teratoma", "Adult Central Nervous System Mature Teratoma", "central nervous system mature teratoma of adults"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult central nervous system mature teratoma", "shortest_name_length": 44}
{"curie": "UMLS:C4687706", "names": ["Benign Pericardial Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Pericardial Germ Cell Tumor", "shortest_name_length": 34}
{"curie": "MONDO:0033258", "names": ["DFNA71", "deafness, autosomal dominant 71", "DEAFNESS, AUTOSOMAL DOMINANT 71", "hearing loss, autosomal dominant 71", "autosomal dominant nonsyndromic deafness 71"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal dominant 71", "shortest_name_length": 6}
{"curie": "MONDO:0018569", "names": ["X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome", "shortest_name_length": 76}
{"curie": "MONDO:0007779", "names": ["ADOS", "GBBB2", "G syndrome", "BBB syndrome", "GBBB syndrome", "Opitz Bbbg syndrome", "Opitz-Frias syndrome", "Opitz-G syndrome, type 2", "Opitz GBBB syndrome, type 2", "Opitz GBBB syndrome, type II", "hypospadias-dysphagia syndrome", "telecanthus-hypospadias syndrome", "autosomal dominant Opitz syndrome", "hypertelorism-hypospadias syndrome", "autosomal dominant Opitz BBB/G syndrome", "autosomal dominant Opitz G/BBB syndrome", "Opitz GBBB syndrome, autosomal dominant", "Opitz G/BBB syndrome, autosomal dominant", "telecanthus with associated abnormalities", "Opitz oculogenitolaryngeal syndrome, type 2", "chromosome 22Q11.2 deletion syndrome, Opitz phenotype", "hypertelorism with esophageal Abnormality and hypospadias"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant Opitz G/BBB syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0012697", "names": ["OTSC7", "OTOSCLEROSIS 7", "Otosclerosis 7", "otosclerosis 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "otosclerosis 7", "shortest_name_length": 5}
{"curie": "MONDO:0043195", "names": ["Rubinstein Taybi like syndrome", "Broad terminal phalanges of the thumbs and great toes, antimongoloid slant of the palpebral fissures, and characteristic beaked noses"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rubinstein Taybi like syndrome", "shortest_name_length": 30}
{"curie": "MONDO:0013021", "names": ["DIRA", "OMPP", "Interleukin-1 receptor antagonist deficiency", "INTERLEUKIN 1 RECEPTOR ANTAGONIST DEFICIENCY", "Interleukin 1 receptor antagonist deficiency", "Deficiency of interleukin-1 receptor antagonist", "deficiency of interleukin-1 receptor antagonist", "Deficiency Of Interleukin 1 Receptor Antagonist", "Deficiency of interleukin(IL)-1 receptor antagonist", "deficiency of the Interleukin-1 receptor antagonist", "Deficiency of the interleukin-1 receptor antagonist", "Deficiency of the Interleukin-1 Receptor Antagonist", "Deficiency of interleukin 1 receptor antagonist [DIRA]", "Deficiency of interleukin-1 receptor antagonist (DIRA)", "Sterile multifocal osteomyelitis with periostitis and pustulosis", "sterile multifocal osteomyelitis with periostitis and pustulosis", "OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS", "osteomyelitis, STERILE multifocal, with periostitis and pustulosis", "Osteomyelitis, sterile multifocal, with periostitis and pustulosis", "OMPP - sterile osteomyelitis, multifocal with periostitis and pustulosis", "Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder)", "Autoinflammatory disease due to interleukin-1 receptor antagonist deficiency", "Autoinflammatory Disease due to Interleukin-1 Receptor Antagonist Deficiency", "autoinflammatory disease due to interleukin-1 receptor antagonist deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sterile multifocal osteomyelitis with periostitis and pustulosis", "shortest_name_length": 4}
{"curie": "MONDO:0006679", "names": ["Bladder obstruction", "bladder obstruction", "Bladder Obstruction", "obstruction bladder", "Bladder Neck Obstruction", "BLADDER NECK OBSTRUCTION", "Obstruction;bladder neck", "bladder neck obstruction", "Bladder neck obstruction", "Bladder-neck obstruction", "bladder-neck obstruction", "bladder-neck; obstruction", "obstruction; bladder-neck", "Bladder Outlet Obstruction", "bladder outlet obstruction", "Bladder outlet obstruction", "Urinary Outlet Obstruction", "Urinary bladder obstruction", "OBSTRUCTION URINARY BLADDER", "BLADDER URINARY OBSTRUCTION", "URINARY BLADDER OBSTRUCTION", "Obstruction urinary bladder", "Obstruction of bladder outlet", "Bladder neck obstruction, NOS", "BNO - Bladder neck obstruction", "BLADDER NECK URINARY OBSTRUCTION", "Urinary Bladder Neck Obstruction", "urinary bladder neck obstruction", "Vesicourethral orifice obstruction", "obstruction; vesicourethral orifice", "vesicourethral orifice; obstruction", "Bladder neck obstruction (disorder)", "bladder neck obstruction (diagnosis)", "Bladder outlet obstruction (disorder)", "bladder outlet obstruction (diagnosis)", "Vesicourethral orifice obstruction, NOS", "Obstruction of bladder neck or vesicourethral orifice", "obstruction of bladder neck or vesicourethral orifice"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder neck obstruction", "shortest_name_length": 19}
{"curie": "UMLS:C1334014", "names": ["High grade flat intraepithelial neoplasia", "Glandular intraepithelial neoplasia grade III", "Grade III Glandular Intraepithelial Neoplasia", "High Grade Glandular Intraepithelial Neoplasia", "High grade glandular intraepithelial neoplasia", "Glandular intraepithelial neoplasia, grade III", "Glandular intraepithelial neoplasia, high grade", "High grade glandular intraepithelial neoplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High grade glandular intraepithelial neoplasia", "shortest_name_length": 41}
{"curie": "MONDO:0013842", "names": ["CORTRD2", "cortisone reductase deficiency 2", "CORTISONE REDUCTASE DEFICIENCY 2", "cortisone reductase deficiency type 2", "Cortisone Reductase Deficiency Type 2", "HSD11B1 cortisone reductase deficiency", "Hyperandrogenism due to cortisone reductase deficiency", "11-beta-hydroxysteroid dehydrogenase deficiency type 1", "11-beta-hydroxysteroid dehydrogenase type 1 deficiency", "11-Beta-Hydroxysteroid Dehydrogenase Type 1 Deficiency", "cortisone reductase deficiency caused by mutation in HSD11B1", "Hyperandrogenism due to cortisone reductase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cortisone reductase deficiency 2", "shortest_name_length": 7}
{"curie": "MONDO:0011536", "names": ["OPA4", "Optic Atrophy 4", "optic atrophy 4", "OPTIC ATROPHY 4", "OPTIC ATROPHY 4 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "optic atrophy 4", "shortest_name_length": 4}
{"curie": "UMLS:C2349148", "names": ["Adrenal Cortex Low-Grade Carcinoma", "Adrenal Cortex Low Grade Carcinoma", "Adrenal Cortical Low-Grade Carcinoma", "Adrenal Cortical Low Grade Carcinoma", "Well Differentiated Adrenal Cortex Cancer", "Well Differentiated Adrenal Cortex Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adrenal Cortical Low Grade Carcinoma", "shortest_name_length": 34}
{"curie": "UMLS:C4520992", "names": ["Stage IVB Lip Cancer", "Stage IVB Lip Carcinoma", "Stage IVB Carcinoma of Lip", "Stage IVB Lip Cancer AJCC v7", "Stage IVB Lip Cancer AJCC v6", "Stage IVB Carcinoma of the Lip", "Stage IVB Lip Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Lip Cancer AJCC v6 and v7", "shortest_name_length": 20}
{"curie": "MONDO:0014550", "names": ["LQT15", "long QT syndrome 15", "LONG QT SYNDROME 15", "CALM2 long QT syndrome", "long QT syndrome type 15", "long QT syndrome caused by mutation in CALM2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "long QT syndrome 15", "shortest_name_length": 5}
{"curie": "UMLS:C4054365", "names": ["Simian Virus 40 Associated Nephrotic Syndrome", "Nephrotic Syndrome - Simian Virus 40 Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - Simian Virus 40 Associated", "shortest_name_length": 45}
{"curie": "MONDO:0042968", "names": ["partial duplication of chromosome 12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of chromosome 12", "shortest_name_length": 36}
{"curie": "MONDO:0007134", "names": ["ODP", "Cooks syndrome", "COOKS SYNDROME", "Cooks syndrome (disorder)", "Anonychia and absence-hypoplasia of distal phalanges", "anonychia and absence/hypoplasia of distal phalanges", "ANONYCHIA-ONYCHODYSTROPHY WITH HYPOPLASIA OR ABSENCE OF DISTAL PHALANGES", "anonychia-onychodystrophy with hypoplasia or absence of distal phalanges", "Anonychia-onychodystrophy with hypoplasia or absence of distal phalanges", "Anonychia-onychodystrophy with hypoplasia or absence of distal phalanges syndrome", "anonychia-onychodystrophy with hypoplasia or absence of distal phalanges syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cooks syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C4763648", "names": ["Refractory Polymorphic Post-Transplant Lymphoproliferative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Polymorphic Post-Transplant Lymphoproliferative Disorder", "shortest_name_length": 67}
{"curie": "MONDO:0007791", "names": ["FBH1", "Fhh1", "HHC1", "FHH type 1", "hypercalcemia, familial benign", "familial benign hypercalcemia 1", "hypocalciuric hypercalcemia type I", "hpocalciuric hypercalcemia, type I", "familial benign hypercalcemia type 1", "Acquired hypocalciuric hypercalcemia", "Hypocalciuric Hypercalcemia, Acquired", "Acquired hypocalciuric hypercalcaemia", "HYPOCALCIURIC HYPERCALCEMIA, ACQUIRED", "hypercalcemia, familial benign type 1", "hypocalciuric hypercalcemia, acquired", "familial hypocalciuric hypercalcemia 1", "CASR familial hypocalciuric hypercalcemia", "familial hypocalciuric hypercalcemia type 1", "familial hypocalciuric hypercalcemia type I", "Hypocalciuric hypercalcemia, familial, type 1", "hypocalciuric hypercalcemia, familial, type 1", "hypocalciuric hypercalcemia, familial, type I", "Acquired hypocalciuric hypercalcemia (disorder)", "familial hypocalciuric hypercalcemia caused by mutation in CASR"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial hypocalciuric hypercalcemia 1", "shortest_name_length": 4}
{"curie": "UMLS:C0221065", "names": ["DANA SYNDROME", "LICHTHEIM SYNDROME", "Lichtheim's disease", "PUTNAM-DANA SYNDROME", "Putnam-Dana syndrome", "Dana-Putnam syndrome", "combined system disease", "COMBINED SYSTEM DISEASE", "Combined systems disease", "Posterolateral sclerosis", "combined systems disease", "POSTEROLATERAL SCLEROSIS", "subacute combined degeneration", "SUBACUTE COMBINED DEGENERATION", "Subacute combined degeneration", "combined degeneration subacute", "Subacute Combined Degeneration", "Neuropathy vitamin B12 deficiency", "Vitamin B12 deficiency neuropathy", "Neuropathy, vitamin B12 deficiency", "Vitamin B>12< deficiency neuropathy", "SACD - Subacute combined degeneration", "Subacute Combined Neuropathy Degeneration", "Neuropathy, Subacute Combined Degeneration", "SPINAL CORD, SUBACUTE COMBINED DEGENERATION", "Vitamin B<sub>12</sub> deficiency neuropathy", "Vitamin B12 deficiency disease of spinal cord", "Neuromyelopathy due to vitamin B12 deficiency", "subacute combined degeneration of spinal cord", "Subacute combined degeneration of spinal cord", "Vitamin B12 deficiency nervous system syndrome", "Vitamin B>12< deficiency disease of spinal cord", "Subacute combined degeneration of spinal cord, NOS", "Subacute combined degeneration of spinal cord syndrome", "Vitamin B<sub>12</sub> deficiency disease of spinal cord", "Subacute combined degeneration of spinal cord (disorder)", "subacute combined degeneration of spinal cord (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subacute Combined Degeneration", "shortest_name_length": 13}
{"curie": "MONDO:0012789", "names": ["DYT16", "DYT-PRKRA", "Dystonia 16", "DYSTONIA 16", "dystonia 16", "dystonia type 16", "Dystonia 16 (disorder)", "DYSTONIA 16 (disorder)", "PRKRA dystonic disorder", "Early-onset dystonia parkinsonism", "early-onset dystonia parkinsonism", "Young-onset dystonia-(parkinsonism)", "dystonic disorder caused by mutation in PRKRA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dystonia 16", "shortest_name_length": 5}
{"curie": "MONDO:0015632", "names": ["FASTKD2-related infantile mitochondrial encephalomyopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FASTKD2-related infantile mitochondrial encephalomyopathy", "shortest_name_length": 57}
{"curie": "MONDO:0002956", "names": ["Cystic basal cell carcinoma", "Cystic Basal Cell Carcinoma", "cystic basal cell carcinoma", "skin cystic basal cell carcinoma", "Skin Cystic Basal Cell Carcinoma", "Cystic basal cell carcinoma (disorder)", "Cystic basal cell carcinoma (diagnosis)", "skin neoplasm malignant carcinoma basal cell cystic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin cystic basal cell carcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C1167724", "names": ["Hepatic cancer stage IV"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatic cancer stage IV", "shortest_name_length": 23}
{"curie": "UMLS:C4725812", "names": ["Recurrent Malignant Soft Tissue Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Malignant Soft Tissue Neoplasm", "shortest_name_length": 40}
{"curie": "UMLS:C0854121", "names": ["Gastrointestinal motility disorder", "Gastrointestinal motility disorder NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal motility disorder", "shortest_name_length": 34}
{"curie": "MONDO:0015990", "names": ["focal, segmental or multifocal dystonia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal, segmental or multifocal dystonia", "shortest_name_length": 39}
{"curie": "UMLS:C5237456", "names": ["Advanced Undifferentiated Pleomorphic Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Undifferentiated Pleomorphic Sarcoma", "shortest_name_length": 45}
{"curie": "MONDO:0014632", "names": ["HLD10", "PYCR2 leukodystrophy", "hypomyelinating leukodystrophy 10", "LEUKODYSTROPHY, HYPOMYELINATING, 10", "leukodystrophy, hypomyelinating, 10", "hypomyelinating leukodystrophy type 10", "leukodystrophy, hypomyelinating, type 10", "leukodystrophy caused by mutation in PYCR2", "PYCR2-related microcephaly-progressive leukoencephalopathy", "PYCR2-related microcephaly, progressive leucoencephalopathy", "PYCR2-related microcephaly, progressive leukoencephalopathy", "Pyrroline-5-carboxylate reductase 2 related microcephaly, progressive leucoencephalopathy", "Pyrroline-5-carboxylate reductase 2 related microcephaly, progressive leukoencephalopathy", "Pyrroline-5-carboxylate reductase 2 related microcephaly, progressive leukoencephalopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypomyelinating leukodystrophy 10", "shortest_name_length": 5}
{"curie": "UMLS:C0334042", "names": ["Chondroid metaplasia", "Cartilaginous Metaplasia", "Cartilaginous metaplasia", "CARTILAGINOUS METAPLASIAS", "Metaplasia, cartilaginous", "Cartilaginous Metaplasias", "Cartilaginous metaplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cartilaginous metaplasia", "shortest_name_length": 20}
{"curie": "MONDO:0014678", "names": ["MRD39", "CHROMOSOME 2p25.3 DELETION SYNDROME", "chromosome 2P25.3 deletion syndrome", "chromosome 2P25.3 Duplication syndrome", "CHROMOSOME 2p25.3 DUPLICATION SYNDROME", "autosomal dominant mental retardation 39", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 39", "mental retardation, autosomal dominant 39", "Mental Retardation, Autosomal Dominant 39", "autosomal dominant intellectual disability 39", "intellectual disability, autosomal dominant 39", "mental retardation, autosomal dominant type 39", "intellectual disability, autosomal dominant type 39", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 39, AND OBESITY", "autosomal dominant intellectual developmental disorder 39", "intellectual developmental disorder, autosomal dominant 39", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 39", "autosomal dominant non-syndromic intellectual disability 39", "MYT1L autosomal dominant non-syndromic intellectual disability", "autosomal dominant non-syndromic intellectual disability caused by mutation in MYT1L"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 39", "shortest_name_length": 5}
{"curie": "UMLS:C4289295", "names": ["Fallopian Tube Lymphoma", "Primary Fallopian Tube Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fallopian Tube Lymphoma", "shortest_name_length": 23}
{"curie": "MONDO:0001523", "names": ["Eye luxation", "Luxation of eye", "luxation of eye", "eye; dislocation", "dislocation; eye", "Luxation of globe", "luxation of globe", "Luxation of eye (disorder)", "luxation of globe (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "luxation of globe", "shortest_name_length": 12}
{"curie": "UMLS:C1709552", "names": ["PitNET/Microadenoma", "Pituitary Gland Microadenoma", "Pituitary Neuroendocrine Tumor/Microadenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pituitary Neuroendocrine Tumor/Microadenoma", "shortest_name_length": 19}
{"curie": "MONDO:0015103", "names": ["PVA/ADA, Fallot type", "APV/ADA, Fallot type", "absence of pulmonary valve-Fallot tetralogy-absence of ductus arteriosus syndrome", "pulmonary valve agenesis-tetralogy of fallot-absence of ductus arteriosus syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary valve agenesis-tetralogy of fallot-absence of ductus arteriosus syndrome", "shortest_name_length": 20}
{"curie": "UMLS:C4744460", "names": ["Unresectable Digestive System Neuroendocrine Carcinoma", "Unresectable Gastrointestinal System Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Digestive System Neuroendocrine Carcinoma", "shortest_name_length": 54}
{"curie": "MONDO:0019422", "names": ["X-linked intellectual disability Stevenson type", "X-linked intellectual disability, Stevenson type", "X-linked intellectual disability Stevenson type (disorder)", "X-linked intellectual disability Stevenson type (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability, Stevenson type", "shortest_name_length": 47}
{"curie": "MONDO:0007128", "names": ["erythema annular", "annular erythema", "Annular Erythema", "Annular erythema", "ANNULAR ERYTHEMA", "Erythema annulare", "annulare erythema", "Figurate erythema", "erythema annulare", "ERYTHEMA ANNULARE", "annulare; erythema", "erythema; annulare", "Annular erythema (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "annular erythema", "shortest_name_length": 16}
{"curie": "MONDO:0024321", "names": ["GPIBD", "disorder of GPI anchor biosynthesis", "GPI anchor biosynthetic process disease", "disorder of GPI anchor biosynthetic process", "glycosylphosphatidylinositol biosynthesis defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of GPI anchor biosynthesis", "shortest_name_length": 5}
{"curie": "UMLS:C4524635", "names": ["Esophageal Adenocarcinoma by AJCC v8 pTNM Stage", "Esophageal Adenocarcinoma Tumor Stage Pathologic", "Esophageal Adenocarcinoma by AJCC v8 Pathologic Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Adenocarcinoma by AJCC v8 Pathologic Stage", "shortest_name_length": 47}
{"curie": "MONDO:0002736", "names": ["ampulla of vater mucinous adenocarcinoma", "ampulla of Vater mucinous adenocarcinoma", "Ampulla of Vater Mucinous Adenocarcinoma", "hepatopancreatic ampulla mucinous adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ampulla of vater mucinous adenocarcinoma", "shortest_name_length": 40}
{"curie": "UMLS:C1336285", "names": ["stage II extragonadal seminoma", "Stage II Extragonadal Seminoma", "Stage II Extragonadal Primary Seminoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Extragonadal Seminoma", "shortest_name_length": 30}
{"curie": "MONDO:0020238", "names": ["genetic vitreoretinal disease", "genetic vitreous-retinal disease", "inherited vitreous-retinal disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited vitreous-retinal disease", "shortest_name_length": 29}
{"curie": "MONDO:0003368", "names": ["prostate leiomyosarcoma", "Prostate Leiomyosarcoma", "Leiomyosarcoma of Prostate", "leiomyosarcoma of prostate", "prostate gland leiomyosarcoma", "leiomyosarcoma of the prostate", "Leiomyosarcoma of the Prostate", "leiomyosarcoma of prostate gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate leiomyosarcoma", "shortest_name_length": 23}
{"curie": "UMLS:C4727193", "names": ["Refractory Small Intestinal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Small Intestinal Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0015775", "names": ["non-rhizomelic chondrodysplasia punctata"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-rhizomelic chondrodysplasia punctata", "shortest_name_length": 40}
{"curie": "UMLS:C1960448", "names": ["Hyperammonemic encephalopathy", "Hyperammonaemic encephalopathy", "toxic encephalopathy hyperammonemic", "Hyperammonemic encephalopathy (disorder)", "Hyperammonemic encephalopathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyperammonemic encephalopathy", "shortest_name_length": 29}
{"curie": "MONDO:0026721", "names": ["MC1DN30", "nuclear type mitochondrial complex I deficiency 30", "mitochondrial complex 1 deficiency, nuclear type 30", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 30"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 30", "shortest_name_length": 7}
{"curie": "UMLS:C0585012", "names": ["Gastric stenosis", "Gastric Stenosis", "gastric stenosis", "stomach stenosis", "Stomach stricture", "stomach; stenosis", "stenosis; stomach", "Gastric stricture", "gastric stricture", "stomach strictures", "stricture; stomach", "stomach; stricture", "gastric strictures", "stenosis of stomach", "Stenosis of stomach", "Gastric stenosis NOS", "gastric stenosis (diagnosis)", "Stenosis of stomach (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Stenosis", "shortest_name_length": 16}
{"curie": "UMLS:C4524716", "names": ["Clinical Stage III Gastroesophageal Junction Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage III Gastroesophageal Junction Adenocarcinoma AJCC v8", "shortest_name_length": 67}
{"curie": "MONDO:0018078", "names": ["soft part sarcoma", "Soft tissue sarcoma", "soft tissue sarcoma", "Soft Tissue Sarcoma", "sarcoma soft tissue", "sarcoma; soft tissue", "soft tissue; sarcoma", "Soft tissue sarcomas", "sarcomas soft tissue", "Sarcoma, Soft Tissue", "soft tissue sarcomas", "Sarcoma of soft tissue", "Sarcoma of Soft Tissue", "sarcoma of soft tissue", "Connective Tissue Sarcoma", "connective tissue sarcoma", "Sarcoma of the Soft Tissue", "sarcoma of the soft tissue", "malignant mesenchymal tumor", "malignant soft tissue tumor", "malignant soft tissue tumors", "Non-Rhabdo. soft tissue sarcoma", "non-Rhabdo. soft tissue sarcoma", "Sarcoma of soft tissue (disorder)", "sarcoma of soft tissue (diagnosis)", "Non-rhabdomyosarcoma soft-tissue sarcoma", "Non-Rhabdomyosarcoma soft tissue sarcoma, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "soft tissue sarcoma", "shortest_name_length": 17}
{"curie": "MONDO:0011154", "names": ["PAFD", "AFD- Palagonia type", "Palagonia form of AFD", "acrofacial dysostosis Palagonia type", "Acrofacial dysostosis Palagonia type", "acrofacial dysostosis, Patagonia type", "acrofacial dysostosis, Palagonia type", "ACROFACIAL DYSOSTOSIS, PALAGONIA TYPE", "Acrofacial dysostosis, Palagonia type", "Palagonia type of acrofacial dysostosis", "Acrofacial dysostosis Palagonia type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acrofacial dysostosis, Palagonia type", "shortest_name_length": 4}
{"curie": "MONDO:0010188", "names": ["VED", "AVED", "FRIEDREICH-LIKE ATAXIA", "Friedreich-like ataxia", "Friedreich-Like Ataxia", "Isolated vitamin E deficiency", "isolated vitamin E deficiency", "Ataxia with vitamin E deficiency", "ATAXIA WITH VITAMIN E DEFICIENCY", "ataxia with vitamin E deficiency", "Familial isolated vitamin E deficiency", "familial isolated vitamin E deficiency", "Familial Isolated Vitamin E Deficiency", "VITAMIN E DEFICIENCY, FAMILIAL ISOLATED", "Ataxia with Isolated Vitamin E Deficiency", "ataxia with isolated vitamin E deficiency", "familial isolated deficiency of vitamin E", "Ataxia with isolated vitamin E deficiency", "Familial isolated deficiency of vitamin E", "Vitamin E, Familial Isolated Deficiency of", "vitamin E, familial isolated deficiency OF", "Ataxia with vitamin E deficiency (disorder)", "familial isolated deficiency of vitamin type E", "Friedreich-like ataxia with selective vitamin E deficiency", "ATAXIA, FRIEDREICH-LIKE, WITH SELECTIVE VITAMIN E DEFICIENCY", "ataxia, Friedreich-like, with selective vitamin E deficiency", "Ataxia, Friedreich-Like, with Selective Vitamin E Deficiency", "Friedreich Ataxia Phenotype with Selective Vitamin E Deficiency", "Friedreich ataxia phenotype with selective vitamin E deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial isolated deficiency of vitamin E", "shortest_name_length": 3}
{"curie": "UMLS:C4553746", "names": ["Stage IIIC Primary Peritoneal Cancer", "Stage IIIC Primary Peritoneal Cancer AJCC v8", "Stage IIIC Primary Peritoneal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Primary Peritoneal Cancer AJCC v8", "shortest_name_length": 36}
{"curie": "UMLS:C5667137", "names": ["Cervical Cancer by FIGO Stage 2009", "Cervical Carcinoma by FIGO Stage 2009"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Cancer by FIGO Stage 2009", "shortest_name_length": 34}
{"curie": "UMLS:C0521496", "names": ["Application site infection", "application site disorder infection", "Application site infection (disorder)", "Application site infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Application site infection", "shortest_name_length": 26}
{"curie": "MONDO:0700154", "names": ["canine rhabdomyosarcoma", "Canine Rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canine rhabdomyosarcoma", "shortest_name_length": 23}
{"curie": "MONDO:0018938", "names": ["MPS4", "MPSIV", "Morquio", "Morquio disease", "Morquio Disease", "morquio disease", "Disease, Morquio", "Morquios Disease", "Morquio Syndrome", "morquio syndrome", "MORQUIO SYNDROME", "Morquio syndrome", "Morquio's Disease", "Morquio A disease", "morquios syndrome", "morquio's disease", "Syndrome, Morquio", "KERATANSULFATURIA", "Morquios Syndrome", "keratansulfaturia", "Morquio Syndromes", "Syndromes, Morquio", "Morquio's syndrome", "Keratan sulfaturia", "Morquio's Syndrome", "Morquio syndrome A", "morquio's syndrome", "syndrome morquio's", "Disease, Morquio's", "Syndrome, Morquio's", "Keratan sulphaturia", "Morquio disease, NOS", "chondroosteodystrophy", "Osteochondrodystrophy", "osteochondrodysplasia", "Morquio syndrome, NOS", "osteochondrodystrophy", "Chondro-osteodystrophy", "chondro-osteodystrophy", "Chondrodystrophia tarda", "Mucopolysaccharidosis 4", "chondrodystrophia tarda", "Morquio-Suarez syndrome", "Morquio-Ullrich disease", "mucopolysaccharidosis IV", "MUCOPOLYSACCHARIDOSIS IV", "MORQUIO-ULLRICH SYNDROME", "KS mucopolysaccharidosis", "eccentrochondrodysplasia", "Mucopolysaccharidosis IV", "atypical chondrodystrophy", "Atypical chondrodystrophy", "familial osseous dystrophy", "Morquio-Brailsford disease", "Familial osseous dystrophy", "MORQUIO-BRAILSFORD SYNDROME", "MPS IV - Morquio syndrome B", "Morquio syndrome or disease", "Morquio syndrome (disorder)", "hereditary chondrodysplasia", "MPS IV - Morquio syndrome A", "Brailsford-Morquio syndrome", "mucopolysaccharidosis type 4", "Mucopolysaccharidosis type 4", "mucopolysaccharidosis type IV", "Mucopolysaccharidosis, MPS-IV", "Mucopolysaccharidosis type IV", "spondylo-epiphyseal dysplasia", "mucopolysaccharidosis, MPS-IV", "eccentroosteochondrodysplasia", "Mucopolysaccharidosis Type IV", "Eccentroosteochondrodysplasia", "type IV; mucopolysaccharidosis", "Type IV, Mucopolysaccharidosis", "eccentro-osteochondrodysplasia", "Eccentroosteochondrodysplasias", "Eccentro-Osteochondrodysplasia", "mucopolysaccharidosis type IVB", "Eccentro Osteochondrodysplasia", "Brailsford syndrome or disease", "Familial osteochondrodystrophy", "Mucopolysaccharidosis, type IV", "Mucopolysaccharidosis Type IVs", "IV, Mucopolysaccharidosis Type", "mucopolysaccharidosis type IVA", "osteochondrodystrophy; familial", "familial; osteochondrodystrophy", "IVs, Mucopolysaccharidosis Type", "mucopolysaccharidosis, MPS-IV-A", "Type IVs, Mucopolysaccharidosis", "Eccentro-Osteochondrodysplasias", "Osteochondrodystrophia deformans", "osteochondrodystrophia deformans", "hereditary osteochondrodystrophy", "Hereditary enchondral dysostosis", "osteochondrodystrophy (diagnosis)", "chondrodystrophia congenita tarda", "Morquio-Ullrich syndrome or disease", "deficiency of chondroitinsulphatase", "galactosamine-6-sulfatase deficiency", "mucopolysaccharide storage disease IV", "mucopolysaccharidosis (MPS) IV (A, B)", "Morquio-Brailsford syndrome or disease", "Mucopolysaccharidosis, type IV (MPS IV)", "dysostosis enchondralis metaepiphysaria", "mucopolysaccharidosis type IV (diagnosis)", "hereditary polytopic enchondral dysostosis", "OSTEOCHONDRODYSTROPHY DEFORMANS, HEREDITARY", "deficiency of N-acetylgalactosamine-6-sulphatase"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucopolysaccharidosis type 4", "shortest_name_length": 4}
{"curie": "MONDO:0011210", "names": ["MITOCHONDRIAL INTERMEMBRANE SPACE PROTEIN TIM12, YEAST, HOMOLOG OF", "mitochondrial intermembrane space protein Tim12, yeast, homolog of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial intermembrane space protein Tim12, yeast, homolog of", "shortest_name_length": 66}
{"curie": "MONDO:0021508", "names": ["benign epicardial tumor", "Benign Epicardial Tumor", "Benign Tumor of Epicardium", "benign epicardial neoplasm", "Benign Epicardial Neoplasm", "epicardium benign neoplasm", "benign tumor of epicardium", "Benign neoplasm of epicardium", "Benign Neoplasm of Epicardium", "benign neoplasm of epicardium", "benign tumor of the epicardium", "Benign Tumor of the Epicardium", "benign neoplasm of the epicardium", "Benign Neoplasm of the Epicardium", "Benign neoplasm of epicardium (disorder)", "benign neoplasm of epicardium (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of epicardium", "shortest_name_length": 23}
{"curie": "MONDO:0008808", "names": ["Bronspiegel Zelnick syndrome", "Bronspiegel-Zelnick syndrome", "autosomal recessive aplasia cutis", "ACC with intestinal lymphangiectasia", "ACC WITH INTESTINAL LYMPHANGIECTASIA", "Aplasia cutis congenita intestinal lymphangiectasia", "aplasia cutis congenita intestinal lymphangiectasia", "APLASIA CUTIS CONGENITA WITH INTESTINAL LYMPHANGIECTASIA", "Aplasia Cutis Congenita With Intestinal Lymphangiectasia", "aplasia cutis congenita with intestinal lymphangiectasia", "Aplasia cutis congenita-intestinal lymphangiectasia syndrome", "aplasia cutis congenita-intestinal lymphangiectasia syndrome", "Aplasia cutis congenita with intestinal lymphangiectasia syndrome", "Aplasia cutis congenita with intestinal lymphangiectasia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aplasia cutis congenita-intestinal lymphangiectasia syndrome", "shortest_name_length": 28}
{"curie": "UMLS:C0751760", "names": ["Shift Work Sleep Disorder", "disorder shift sleep work", "Shift-Work Sleep Disorder", "shift work sleep disorder", "Shift-Work Sleep Disorders", "Sleep Disorder, Shift-Work", "Sleep Disorder, Shift Work", "Sleep Disorders, Shift-Work", "organic circadian rhythm sleep disorder shift work type", "organic circadian rhythm sleep disorder, shift work type", "organic circadian rhythm sleep disorder, shift work type (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Shift-Work Sleep Disorder", "shortest_name_length": 25}
{"curie": "MONDO:0007683", "names": ["Grant syndrome", "GRANT SYNDROME", "Grant syndrome (disorder)", "persistent wormian bones, blue sclerae, mandibular hypoplasia, shallow glenoid fossae and campomelia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grant syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0012963", "names": ["MVCD3", "NEPHROPATHY, DIABETIC, SUSCEPTIBILITY TO", "nephropathy, diabetic, susceptibility to", "microvascular complications of diabetes 3", "end-stage renal disease, diabetic, susceptibility to", "END-STAGE RENAL DISEASE, DIABETIC, SUSCEPTIBILITY TO", "ACE microvascular complications of diabetes, susceptibility", "microvascular complications of diabetes, susceptibility to, 3", "MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 3", "microvascular complications of diabetes, susceptibility to, type 3", "microvascular complications of diabetes, susceptibility caused by mutation in ACE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microvascular complications of diabetes, susceptibility to, 3", "shortest_name_length": 5}
{"curie": "MONDO:0004263", "names": ["Pediatric Infratentorial Ependymoblastoma", "childhood infratentorial ependymoblastoma", "Childhood Infratentorial Ependymoblastoma", "pediatric infratentorial ependymoblastoma", "childhood infratentorial embryonal tumor with Multilayered Rosettes, C19MC-altered", "Childhood Infratentorial Embryonal Tumor with Multilayered Rosettes, C19MC-Altered", "childhood infratentorial embryonal tumor with multilayered rosettes, C19MC-altered"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pediatric infratentorial ependymoblastoma", "shortest_name_length": 41}
{"curie": "UMLS:C3828476", "names": ["Primary hypoparathyroidism", "Primary Hypoparathyroidism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary hypoparathyroidism", "shortest_name_length": 26}
{"curie": "MONDO:0015401", "names": ["maxillary arteriovenous malformation", "Maxillary arteriovenous malformation", "Arteriovenous malformation of maxilla", "arteriovenous malformation of maxilla", "Arteriovenous malformation of maxilla (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maxillary arteriovenous malformation", "shortest_name_length": 36}
{"curie": "UMLS:C0233754", "names": ["derealisation", "Derealization", "derealization", "Derealisation", "Feeling unreal", "FEELING UNREAL", "Derealizations", "feelings unreality", "feeling of unreality", "Feeling of unreality", "Derealization (finding)", "feel that surroundings are unreal", "feel that surroundings are unreal (symptom)", "feel that surroundings are unreal (derealization)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Derealization", "shortest_name_length": 13}
{"curie": "MONDO:0003747", "names": ["telangiectatic glomangioma", "Telangiectatic Glomangioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "telangiectatic glomangioma", "shortest_name_length": 26}
{"curie": "UMLS:C0699728", "names": ["Chronic Progressive Chorea", "Chronic progressive chorea", "Chorea, Chronic Progressive", "Progressive Chorea, Chronic", "Chronic Progressive Choreas", "Progressive Choreas, Chronic", "Choreas, Chronic Progressive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic progressive chorea", "shortest_name_length": 26}
{"curie": "UMLS:C0027661", "names": ["hormone related neoplasm", "Hormone-Dependent Neoplasm", "Hormone-Dependent Neoplasms", "Neoplasm, Hormone-Dependent", "Hormone Dependent Neoplasms", "Neoplasms, Hormone-Dependent", "Neoplasms, Hormone Dependent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplasms, Hormone-Dependent", "shortest_name_length": 24}
{"curie": "MONDO:0015508", "names": ["genetic parenchymatous liver disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genetic parenchymatous liver disease", "shortest_name_length": 36}
{"curie": "UMLS:C0406486", "names": ["Ocular rosacea", "rosacea ocular", "Ocular Rosacea", "ocular rosacea", "Rosacea, Ocular", "Ocular rosacea (disorder)", "ocular rosacea (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ocular Rosacea", "shortest_name_length": 14}
{"curie": "MONDO:0023203", "names": ["Fuchs gyrate atrophy", "Fuchs atrophia gyrata chorioideae et retinae", "Fuchs gyrate atrophy of the choroid and retina"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fuchs atrophia gyrata chorioideae et retinae", "shortest_name_length": 20}
{"curie": "MONDO:0008404", "names": ["SENS", "Sen Syndrome", "SEN SYNDROME", "Sen syndrome", "Finlay-Marks Syndrome", "Finlay Marks syndrome", "FINLAY-MARKS SYNDROME", "Finlay-Marks syndrome", "Scalp-Ear-Nipple Syndrome", "scalp-EAR-nipple syndrome", "scalp-ear-nipple syndrome", "Scalp ear nipple syndrome", "SCALP-EAR-NIPPLE SYNDROME", "scalp ear nipple syndrome", "Scalp-ear-nipple syndrome", "Scalp, ear, nipple syndrome", "Scalp, ear, nipple syndrome (disorder)", "hereditary syndrome of lumpy scalp, odd ears and rudimentary nipples", "Hereditary syndrome of lumpy scalp, odd ears and rudimentary nipples"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scalp-ear-nipple syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C1336253", "names": ["Stage III Lip Cancer", "Stage III Cancer of Lip", "Stage III Lip Carcinoma", "Stage III Carcinoma of Lip", "Stage III Cancer of the Lip", "Stage III Lip Cancer AJCC v7", "Stage III Lip Cancer AJCC v6", "Stage III Carcinoma of the Lip", "Stage III Lip Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Lip Cancer AJCC v6 and v7", "shortest_name_length": 20}
{"curie": "UMLS:C0041636", "names": ["Umbilical Hernia without Mention of Obstruction or Gangrene", "Umbilical hernia without mention of obstruction or gangrene"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Umbilical hernia without mention of obstruction or gangrene", "shortest_name_length": 59}
{"curie": "UMLS:C0862211", "names": ["Mycosis fungoides/Sezary syndrome stage I", "stage I mycosis fungoides/Sezary syndrome", "mycosis fungoides/Sezary syndrome, stage I", "Stage I Mycosis Fungoides and Sezary Syndrome", "Stage I Mycosis Fungoides and Sézary Syndrome", "stage I mycosis fungoides and the Sezary syndrome", "Stage I Mycosis Fungoides and Sezary Syndrome AJCC v7", "Stage I Mycosis Fungoides and Sézary Syndrome AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mycosis fungoides/Sezary syndrome stage I", "shortest_name_length": 41}
{"curie": "MONDO:0012941", "names": ["IBD25", "inflammatory bowel disease 25", "IL10RB inflammatory bowel disease", "inflammatory bowel disease type 25", "INFLAMMATORY BOWEL DISEASE 25, AUTOSOMAL RECESSIVE", "inflammatory bowel disease 25, autosomal recessive", "Inflammatory Bowel Disease 25, Autosomal Recessive", "inflammatory bowel disease caused by mutation in IL10RB", "INFLAMMATORY BOWEL DISEASE, EARLY-ONSET, AUTOSOMAL RECESSIVE", "inflammatory bowel disease, early-onset, autosomal recessive", "early onset autosomal recessive inflammatory bowel disease 25", "inflammatory bowel disease 25, early onset, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory bowel disease 25", "shortest_name_length": 5}
{"curie": "UMLS:C3899663", "names": ["Favorable Prognosis Hodgkin Lymphoma", "Childhood Favorable Prognosis Hodgkin Lymphoma", "childhood favorable prognosis Hodgkin lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Favorable Prognosis Hodgkin Lymphoma", "shortest_name_length": 36}
{"curie": "UMLS:C1336425", "names": ["Stage IV Major Salivary Gland Cancer without Metastasis", "Stage IV Major Salivary Gland Carcinoma without Metastasis", "Stage IV Carcinoma of Major Salivary Gland without Metastasis", "Stage IV Carcinoma of the Major Salivary Gland without Metastasis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Major Salivary Gland Carcinoma without Metastasis", "shortest_name_length": 55}
{"curie": "MONDO:0013883", "names": ["CMS13", "CMSTA2", "congenital myasthenic syndrome 13", "myasthenic syndrome, congenital, 13", "MYASTHENIC SYNDROME, CONGENITAL, 13", "congenital myasthenic syndrome type 13", "myasthenic syndrome, congenital, type 13", "congenital myasthenic syndrome with tubular aggregates 2", "congenital myasthenic syndrome 13 with tubular aggregates", "MYASTHENIC SYNDROME, CONGENITAL, WITH TUBULAR AGGREGATES 2", "myasthenic syndrome, congenital, with tubular aggregates 2", "myasthenic syndrome, congenital, 13, with tubular aggregates", "DPAGT1 congenital myasthenic syndromes with glycosylation defect", "congenital myasthenic syndromes with glycosylation defect caused by mutation in DPAGT1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myasthenic syndrome 13", "shortest_name_length": 5}
{"curie": "MONDO:0003647", "names": ["atrophic flaccid tympanic membrane", "Atrophic flaccid tympanic membrane", "Atrophic flaccid tympanic membrane (disorder)", "atrophic flaccid tympanic membrane (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrophic flaccid tympanic membrane", "shortest_name_length": 34}
{"curie": "MONDO:0003145", "names": ["pnet", "PNET", "PNETs", "neuroepithelioma", "Neuroepithelioma", "supratentorial PNET", "Supratentorial PNET", "Neuroepithelioma NOS", "Neuroepithelioma, NOS", "Neuroectodermal Tumor", "CNS/supratentorial PNET", "CNS/Supratentorial PNET", "Neuroectodermal Neoplasm", "neuroepithelioma (diagnosis)", "Primitive neuroectodermal tumor", "primitive neuroectodermal tumor", "Primitive Neuroectodermal Tumor", "Primitive Neuroepithelial Tumor", "Neuroectodermal Tumor, Primitive", "Primitive Neuroepithelial Tumors", "Primitive neuroectodermal tumour", "Neuroepithelial Tumor, Primitive", "Primitive Neuroectodermal Tumors", "primitive neuroectodermal tumors", "neuroectodermal primitive tumors", "Tumor, Primitive Neuroectodermal", "Tumor, Primitive Neuroepithelial", "primitive neuroectodermal tumour", "supratent. primitive neuro. tumor", "Neuroepithelial Tumors, Primitive", "Tumors, Primitive Neuroepithelial", "Supratent. primitive neuro. tumor", "Neuroectodermal Tumors, Primitive", "Tumors, Primitive Neuroectodermal", "Primitive Neuroectodermal Neoplasm", "Primitive Neuroepithelial Neoplasm", "Neoplasm, Primitive Neuroepithelial", "[M] Primitive neuroectodermal tumor", "Supratentorial Embryonal Tumor, NOS", "Neuroepithelial Neoplasm, Primitive", "Primitive Neuroepithelial Neoplasms", "Neoplasms, Primitive Neuroepithelial", "[M] Primitive neuroectodermal tumour", "Neuroepithelial Neoplasms, Primitive", "primitive neuroectodermal tumor (PNET)", "PNET - Primitive neuroectodermal tumor", "PNET - Primitive neuroectodermal tumour", "Neuroepithelioma (morphologic abnormality)", "Primitive neuroectodermal tumor (disorder)", "primitive neuroectodermal tumor (diagnosis)", "supratentorial primitive neuroectodermal tumor", "Supratentorial Primitive Neuroectodermal Tumor", "neuroendocrine tumor primitive neuroectodermal", "Supratentorial primitive neuroectodermal tumor", "Supratentorial primitive neuroectodermal tumour", "primitive; neuroectodermal tumor, unspecified site", "neuroectodermal; tumor, primitive, unspecified site", "tumor; neuroectodermal, primitive, unspecified site", "Supratentorial Embryonal Tumor, Not Otherwise Specified", "Supratentorial primitive neuroectodermal tumor (disorder)", "Primitive neuroectodermal tumor (morphologic abnormality)", "Supratentorial primitive neuroectodermal tumor (diagnosis)", "neuroendocrine tumor primitive neuroectodermal supratentorial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "supratentorial primitive neuroectodermal tumor", "shortest_name_length": 4}
{"curie": "OMIM:200300", "names": ["ACETOPHENETIDIN SENSITIVITY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 27}
{"curie": "MONDO:0001666", "names": ["Bruch's membrane inherited retinal dystrophy", "inherited retinal dystrophy of Bruch's membrane", "Dystrophies primarily involving Bruch's membrane", "retinal dystrophies primarily involving Bruch membrane", "retinal dystrophies primarily involving Bruch's membrane", "Retinal dystrophies primarily involving Bruch's membrane"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal dystrophies primarily involving Bruch's membrane", "shortest_name_length": 44}
{"curie": "MONDO:0014940", "names": ["NADGP", "neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset", "NEURODEGENERATION WITH ATAXIA, DYSTONIA, AND GAZE PALSY, CHILDHOOD-ONSET", "neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset; NADGP"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset", "shortest_name_length": 5}
{"curie": "MONDO:0015438", "names": ["R22", "Ring 22", "r(22) syndrome", "chromosome 22 ring", "Chromosome 22 ring", "ring chromosome 22", "Ring chromosome 22", "Ring 22, Chromosome", "Ring chromosome type 22", "Ring Chromosome 22 Syndrome", "Ring chromosome 22 syndrome", "Ring chromosome 22 syndrome (disorder)", "Ring chromosome 22 syndrome (diagnosis)", "anomaly of chromosome pair ring 22 syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ring chromosome 22", "shortest_name_length": 3}
{"curie": "MONDO:0005588", "names": ["chemotherapy-induced oral mucositis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chemotherapy-induced oral mucositis", "shortest_name_length": 35}
{"curie": "UMLS:C5556907", "names": ["Parotid Gland Mantle Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parotid Gland Mantle Cell Lymphoma", "shortest_name_length": 34}
{"curie": "MONDO:0032707", "names": ["TPFS", "TURNPENNY-FRY SYNDROME", "turnpenny-fry syndrome", "NEUROCARDIOSKELETAL SYNDROME", "Neurocardioskeletal Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "turnpenny-fry syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0007850", "names": ["autosomal dominant KID syndrome", "KID syndrome, autosomal dominant", "keratitis-ichthyosis -deafness syndrome", "autosomal dominant keratitis-ichthyosis-deafness syndrome", "keratitis-ichthyosis-deafness syndrome, autosomal dominant", "autosomal dominant keratitis-ichthyosis-hearing loss syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant keratitis-ichthyosis-hearing loss syndrome", "shortest_name_length": 31}
{"curie": "MONDO:0009155", "names": ["EEMS", "EEM syndrome", "EEM Syndrome", "EEM SYNDROME", "Ectodermal Dysplasia-Ectrodactyly-Macular Dystrophy", "ectodermal dysplasia, ectrodactyly, and macular dystrophy", "Ectodermal dysplasia, ectrodactyly, and macular dystrophy", "ectodermal dysplasia-ectrodactyly-macular dystrophy syndrome", "Ectodermal dysplasia-ectrodactyly-macular dystrophy syndrome", "ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome", "ECTODERMAL DYSPLASIA, ECTRODACTYLY, AND MACULAR DYSTROPHY SYNDROME", "EEM (ectodermal dysplasia, ectrodactyly, macular dystrophy) syndrome", "Ectodermal dysplasia with ectrodactyly and macular dystrophy syndrome", "Ectodermal dysplasia with ectrodactyly and macular dystrophy syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "EEM syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C4525302", "names": ["Gallbladder cancer", "stage III gallbladder cancer", "Stage III Gallbladder Cancer", "stage III gallbladder cancer AJCC v8", "Stage III Gallbladder Cancer AJCC v8", "stage III gallbladder carcinoma AJCC v8", "Stage III Gallbladder Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Gallbladder Cancer AJCC v8", "shortest_name_length": 18}
{"curie": "MONDO:0015770", "names": ["Congenital hypogonadotropic hypogonadism", "congenital hypogonadotropic hypogonadism", "Congenital Hypogonadotropic Hypogonadism", "Congenital hypogonadotropic hypogonadism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital hypogonadotropic hypogonadism", "shortest_name_length": 40}
{"curie": "MONDO:0700106", "names": ["immune system disorder, non-human animal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immune system disorder, non-human animal", "shortest_name_length": 40}
{"curie": "MONDO:0013862", "names": ["CVID7", "common variable immunodeficiency 7", "immunodeficiency, common variable, 7", "IMMUNODEFICIENCY, COMMON VARIABLE, 7", "immunodeficiency, common variable, type 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency, common variable, 7", "shortest_name_length": 5}
{"curie": "MONDO:0002136", "names": ["eyelid eczema", "Eyelid eczema", "eczema eyelid", "Eczema eyelids", "eczema; eyelid", "eczema eyelids", "eyelid; eczema", "Eczema of eyelid", "eczematous dermatitis of eyelid", "Eczematous dermatitis of eyelid", "Eczematous dermatitis of eyelid (disorder)", "eczematous dermatitis of eyelid (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eczematous dermatitis of eyelid", "shortest_name_length": 13}
{"curie": "UMLS:C4528624", "names": ["Stage IVA Vulvar Cancer", "Stage IVA Vulvar Cancer AJCC v8", "Stage IVA Vulvar Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Vulvar Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "UMLS:C1518064", "names": ["Lymphocyte Predominant Type Hodgkin's Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphocyte Predominant Type Hodgkin's Disease", "shortest_name_length": 45}
{"curie": "UMLS:C0855070", "names": ["Synovial sarcoma metastatic", "Synovial Sarcoma Metastatic", "Metastatic Synovial Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Synovial sarcoma metastatic", "shortest_name_length": 27}
{"curie": "MONDO:0003869", "names": ["Brain Stem Glioma", "brain stem glioma", "pediatric brainstem glioma", "Childhood Brainstem Glioma", "childhood brainstem glioma", "Pediatric Brainstem Glioma", "glioma, childhood brainstem", "Pediatric Brain Stem Glioma", "pediatric brain stem glioma", "childhood brain stem glioma", "brainstem glioma, pediatric", "brainstem glioma, childhood", "Childhood Brain Stem Glioma", "glioma, pediatric brainstem", "glioma, childhood brain stem", "brain stem glioma, pediatric", "brain stem glioma, childhood", "glioma, pediatric brain stem", "childhood glioma of brainstem", "Pediatric Glioma of Brainstem", "Childhood Glioma of Brainstem", "pediatric glioma of brainstem", "brain stem glioma of childhood", "Childhood Glioma of Brain Stem", "childhood glioma of brain stem", "pediatric glioma of brain stem", "Pediatric Glioma of Brain Stem", "gliosarcoma, childhood brainstem", "pediatric glioma of the Brainstem", "Childhood Glioma of the Brainstem", "pediatric glioma of the brainstem", "Pediatric Glioma of the Brainstem", "childhood glioma of the brainstem", "pediatric glioma of the brain stem", "Pediatric Glioma of the Brain Stem", "childhood glioma of the brain stem", "Childhood Glioma of the Brain Stem", "childhood CNS tumor, brainstem glioma", "CNS tumor, pediatric brainstem glioma", "Brain tumor, child: Brain stem glioma", "pediatric CNS tumor, brainstem glioma", "CNS tumor, childhood brainstem glioma", "CNS tumor, brainstem glioma, childhood", "CNS tumor, childhood brain stem glioma", "pediatric brain tumor, brainstem glioma", "CNS tumor, brain stem glioma, childhood", "childhood brain tumor, brainstem glioma", "brain tumor, childhood, brainstem glioma", "childhood brain tumor, brain stem glioma", "brain tumor, pediatric, brainstem glioma", "brain tumor, brainstem glioma, childhood", "brain tumor, brain stem glioma, childhood", "central nervous system tumor, brainstem glioma, childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood brain stem glioma", "shortest_name_length": 17}
{"curie": "MONDO:0006243", "names": ["hepatoid carcinoma", "Hepatoid Carcinoma", "Hepatoid carcinoma", "Hepatoid adenocarcinoma", "Hepatoid Adenocarcinoma", "hepatoid adenocarcinoma", "Hepatoid adenocarcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatoid adenocarcinoma", "shortest_name_length": 18}
{"curie": "MONDO:0012445", "names": ["DFNB59", "autosomal recessive deafness 59", "DEAFNESS, AUTOSOMAL RECESSIVE 59", "deafness, autosomal recessive 59", "Deafness, Autosomal Recessive 59", "deafness, autosomal recessive type 59", "autosomal recessive nonsyndromic deafness 59", "PJVK autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 59", "autosomal recessive nonsyndromic deafness type 59", "autosomal recessive nonsyndromic deafness caused by mutation in PJVK"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 59", "shortest_name_length": 6}
{"curie": "MONDO:0006778", "names": ["HALO NEVI", "Halo Nevi", "halo nevi", "Halo Nevus", "Halo nevus", "halos nevi", "Nevi, Halo", "nevus halo", "halo nevus", "Nevus, Halo", "Halo naevus", "halo naevus", "naevus halo", "Naevus;halo", "Sutton Nevus", "[M]Halo nevus", "[M]Halo naevus", "Sutton's nevus", "Sutton's naevus", "Regressing nevus", "Regressing Nevus", "Regressing naevus", "Perinevoid Vitiligo", "Halo nevus (disorder)", "Perinevoid Leukoderma", "Leukoderma Acquisitum Centrifugum", "Halo nevus (morphologic abnormality)", "LEUKODERMA ACQUISITUM CENTRIFUGUM OF SUTTON", "leukoderma acquisitum Centrifugum of Sutton", "Leukoderma Acquisitum Centrifugum of Sutton"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "halo nevus", "shortest_name_length": 9}
{"curie": "UMLS:C4683592", "names": ["Lugano Classification Stage III Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage III Hodgkin Lymphoma AJCC v8", "shortest_name_length": 56}
{"curie": "MONDO:0019758", "names": ["MIH", "MIHV", "MIHF", "MIH type HPE", "Syntelencephaly", "middle interhemispheric fusion variant", "middle interhemispheric variant of holoprosencephaly", "midline interhemispheric variant of holoprosencephaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "midline interhemispheric variant of holoprosencephaly", "shortest_name_length": 3}
{"curie": "MONDO:0001831", "names": ["irregular astigmatism", "Irregular astigmatism", "Astigmatism, irregular", "Irregular astigmatism (disorder)", "irregular astigmatism (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "irregular astigmatism", "shortest_name_length": 21}
{"curie": "MONDO:0016932", "names": ["Duplication of chromosome 11", "Partial trisomy of chromosome 11", "partial trisomy of chromosome 11", "partial duplication of chromosome 11", "Partial duplication of chromosome 11", "partial duplication of chromosome type 11", "Partial trisomy of chromosome 11 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of chromosome 11", "shortest_name_length": 28}
{"curie": "MONDO:0018918", "names": ["carcinoma of gallbladder and EBT", "carcinoma of gallbladder and extrahepatic biliary tract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma of gallbladder and extrahepatic biliary tract", "shortest_name_length": 32}
{"curie": "UMLS:C1336805", "names": ["Transitional Cell Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transitional Cell Intraepithelial Neoplasia", "shortest_name_length": 43}
{"curie": "UMLS:C0751868", "names": ["Alcohol Withdrawal Induced Major Motor Seizure", "Alcohol Withdrawal-Induced Major Motor Seizure", "Major Motor Seizure, Alcohol Withdrawal-Induced"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alcohol Withdrawal-Induced Major Motor Seizure", "shortest_name_length": 46}
{"curie": "MONDO:0008617", "names": ["IBD11", "Inflammatory Bowel Disease 11", "inflammatory bowel disease 11", "INFLAMMATORY BOWEL DISEASE 11", "inflammatory bowel disease type 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory bowel disease 11", "shortest_name_length": 5}
{"curie": "UMLS:C0877117", "names": ["GASTRITIS CMV", "CMV Gastritis", "CMV-Related Gastritis", "Cytomegaloviral gastritis", "Cytomegalovirus gastritis", "Cytomegalovirus Gastritis", "Cytomegaloviral Gastritis", "Cytomegalovirus-Related Gastritis", "Cytomegaloviral gastritis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cytomegaloviral gastritis", "shortest_name_length": 13}
{"curie": "UMLS:C3272829", "names": ["Colorectal Mantle Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Mantle Cell Lymphoma", "shortest_name_length": 31}
{"curie": "UMLS:C1336918", "names": ["Uterine Corpus Non-Neoplastic Disease", "Uterine Corpus Non-Neoplastic Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Corpus Non-Neoplastic Disorder", "shortest_name_length": 37}
{"curie": "UMLS:C1336973", "names": ["Optic Tract Neoplasm", "neoplasm of optic tract", "neoplasm of optic tract (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplasm of optic tract", "shortest_name_length": 20}
{"curie": "MONDO:0013821", "names": ["CSS4", "MRD16", "COFFIN-SIRIS SYNDROME 4", "COFFIN-SIRIS syndrome 4", "Coffin-Siris syndrome 4", "SMARCA4-related BAFopathy", "SMARCA4 Coffin-Siris syndrome", "autosomal dominant mental retardation 16", "mental retardation, autosomal dominant 16", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 16", "autosomal dominant intellectual disability 16", "intellectual disability, autosomal dominant 16", "mental retardation, autosomal dominant type 16", "intellectual disability, autosomal dominant type 16", "Coffin-Siris syndrome caused by mutation in SMARCA4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 16", "shortest_name_length": 4}
{"curie": "UMLS:C3897510", "names": ["Stage IVC Lip and Oral Cavity Squamous Cell Cancer", "Stage IVC Lip and Oral Cavity Squamous Cell Carcinoma AJCC v6", "Stage IVC Lip and Oral Cavity Squamous Cell Carcinoma AJCC v7", "Stage IVC Lip and Oral Cavity Squamous Cell Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Lip and Oral Cavity Squamous Cell Carcinoma AJCC v6 and v7", "shortest_name_length": 50}
{"curie": "UMLS:C3494424", "names": ["Maxillary Retrusion", "Maxillary Retrusions", "Retrusion, Maxillary", "Retrusions, Maxillary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Maxillary Retrusion", "shortest_name_length": 19}
{"curie": "MONDO:0800030", "names": ["FIPA", "MINAT", "CID-MIA/early-onset IBD", "intestinal atresia, multiple", "familial intestinal polyatresia syndrome", "combined immunodeficiency-enteropathy spectrum", "gastrointestinal defects and immunodeficiency syndrome 1", "multiple intestinal atresia and/or inflammatory bowel disease with or without immunodeficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastrointestinal defects and immunodeficiency syndrome 1", "shortest_name_length": 4}
{"curie": "MONDO:0001869", "names": ["paraurethral gland cancer", "cancer of paraurethral gland", "malignant tumor of paraurethral gland", "malignant paraurethral gland neoplasm", "Malignant tumor of paraurethral gland", "Malignant tumour of paraurethral gland", "malignant neoplasm of paraurethral gland", "Malignant neoplasm of paraurethral gland", "malignant tumor of the paraurethral gland", "malignant tumor of the Paraurethral gland", "Malignant neoplasm of paraurethral glands", "Malignant tumor of paraurethral gland (disorder)", "malignant neoplasm of paraurethral gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paraurethral gland cancer", "shortest_name_length": 25}
{"curie": "MONDO:0010602", "names": ["HEMA", "hem A", "Hemophilia", "Haemophilia", "Hemophilia A", "hemophilia a", "HEMOPHILIA A", "hemophilia A", "Hemophilia As", "A; hemophilia", "hemophilia; A", "haemophilia a", "Subhemophilia", "Haemophilia A", "Hemophilia NOS", "AHG DEFICIENCY", "AHG deficiency", "hemophilia type a", "Hemophilia A, NOS", "hemophilia type A", "classic hemophilia", "Classic Hemophilia", "Haemophilia A, NOS", "Hemophilia, Classic", "HEMOPHILIA, CLASSIC", "hemophilia, classic", "factor 8 deficiency", "Classic Hemophilias", "Hemophilias, Classic", "Hemophilia, familial", "classic hemophilia A", "classical hemophilia", "Classical hemophilia", "hemophilia; classical", "Hemophilia, classical", "Classical haemophilia", "classical; hemophilia", "Hemophilia, hereditary", "Factor VIII Deficiency", "factor VIII deficiency", "AHG deficiency disease", "factor viii hemophilia", "autosomal hemophilia a", "Factor VIII deficiency", "AUTOSOMAL HEMOPHILIA A", "autosomal hemophilia A", "FACTOR VIII DEFICIENCY", "factor viii deficiency", "Deficiency, Factor VIII", "Congenital Hemophilia A", "Hemophilia A, Congenital", "Congenital F8 deficiency", "hemophilia A (diagnosis)", "hemophilia A, congenital", "Congenital Hemophilia As", "Hemophilia As, Congenital", "Hemophilia A (Factor VIII)", "Haemophilia A (Factor VIII)", "Congenital FVIII deficiency", "Reduced factor VIII activity", "Factor 8 Deficiency, Congenital", "FACTOR VIII DISORDER CONGENITAL", "congenital factor viii disorder", "congenital factor VIII disorder", "Congenital factor VIII disorder", "autosomal Factor VIII deficiency", "hemophilia a, X-linked recessive", "Functional factor VIII deficiency", "Sex-linked factor VIII deficiency", "Factor VIII deficiency (disorder)", "Congenital Factor VIII deficiency", "hereditary factor VIII deficiency", "hereditary Factor VIII deficiency", "Congenital factor VIII deficiency", "Hereditary Factor VIII Deficiency", "Hereditary factor VIII deficiency", "Antihemophilic globulin deficiency", "ANTIHEMOPHILIC FACTOR A DEFICIENCY", "ANTIHEMOPHILIC GLOBULIN DEFICIENCY", "Factor VIII Deficiency, Congenital", "factor VIII deficiency (hemophilia)", "anti-hemophilic globulin; deficiency", "deficiency; anti-hemophilic globulin", "hereditary factor VIII deficiency disease", "Congenital factor VIII deficiency disease", "Hereditary factor VIII deficiency disease", "Hereditary Factor VIII Deficiency Disease", "hereditary Factor VIII deficiency disease", "Sex-linked factor VIII deficiency disease", "Hereditary factor VIII deficiency disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemophilia A", "shortest_name_length": 4}
{"curie": "MONDO:0000378", "names": ["Sertoli cell carcinoma", "malignant androblastoma", "Malignant Androblastoma", "malignant Androblastoma", "Malignant androblastoma", "Androblastoma, malignant", "Malignant arrhenoblastoma", "Arrhenoblastoma, malignant", "Malignant Sertoli Cell Tumor", "malignant Sertoli cell tumor", "Sertoli cell tumor, malignant", "SERTOLI CELL TUMOR, MALIGNANT", "malignant androblastoma (diagnosis)", "Androblastoma, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant Sertoli cell tumor", "shortest_name_length": 22}
{"curie": "MONDO:0100057", "names": ["food-dependent exercise-induced anaphylaxis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "food-dependent exercise-induced anaphylaxis", "shortest_name_length": 43}
{"curie": "MONDO:0002039", "names": ["cognitive disease", "cognitive deficit", "COGNITIVE DEFICIT", "disease cognitive", "cognitive deficits", "cognitive diseases", "cognition disorder", "disorder attention", "Cognitive disorder", "Cognitive Disorder", "Attention disorder", "Cognitive Deficits", "cognitive disorder", "attention disorder", "Disorder, Cognition", "attention disorders", "cognitive disorders", "Cognition Disorders", "Cognition disorders", "cognitive; disorder", "Cognitive disorders", "cognition disorders", "Disorders, Cognition", "organic mental disease", "cognitive disorder nos", "Cognitive disorder NOS", "ORGANIC MENTAL DISEASE", "organic mental disorder", "Organic Mental Disorder", "MENTAL DISORDER ORGANIC", "Organic Mental disorder", "disorder mental organic", "Neurocognitive Disorder", "Neurocognitive disorder", "Organic mental disorder", "neurocognitive disorder", "ORGANIC MENTAL DISORDERS", "Neurocognitive Disorders", "Organic Mental Disorders", "Disorder, Neurocognitive", "Mental Disorder, Organic", "Neurocognitive disorders", "organic mental disorders", "Mental Disorders, Organic", "Disorders, Organic Mental", "Disorders, Neurocognitive", "Organic mental disorder NOS", "Organic mental disorder, NOS", "Cognitive disorder (disorder)", "cognitive and memory disorder", "cognitive disorder (diagnosis)", "Cognitive disorder due to disorder", "Organic mental disorder (disorder)", "Neurocognitive disorder (disorder)", "neurocognitive disorder (diagnosis)", "organic mental disorder of unknown etiology", "ORGANIC MENTAL DISORDERS OF UNKNOWN ETIOLOGY", "PROBLEMS WITH COGNITIVE/INTELLECTUAL FUNCTION", "Delirium, Dementia, Amnestic, Cognitive Disorders", "organic mental disorder of unknown etiology (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cognitive disorder", "shortest_name_length": 17}
{"curie": "MONDO:0013091", "names": ["GSD9C", "GSD IXC", "GSD IXc", "GSD type 9C", "GSD type IXc", "glycogenosis type 9C", "glycogenosis type IXc", "Glycogen Storage Disease IXC", "glycogen storage disease IXc", "GLYCOGEN STORAGE DISEASE IXc", "PHKG2 glycogen storage disease", "glycogen storage disease type 9C", "glycogen storage disease type IXc", "PHKG2-related glycogen storage disease type IX", "glycogen storage disease caused by mutation in PHKG2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease IXc", "shortest_name_length": 5}
{"curie": "MONDO:0019561", "names": ["Lupus Profundus", "profundus lupus", "lupus profundus", "panniculitis lupus", "Lupus Panniculitis", "Lupus panniculitis", "lupus panniculitis", "Panniculitis, Lupus", "lupus; panniculitis", "panniculitis; lupus", "Lupus Panniculitides", "Panniculitides, Lupus", "lupus erythematosus profundus", "Lupus Erythematosus Profundus", "Lupus panniculitis (disorder)", "Lupus erythematosus profundus", "lupus panniculitis (diagnosis)", "Lupus erythematosus, profundus", "Lupus Erythematosus Panniculitis", "Lupus erythematosus panniculitis", "lupus erythematosus panniculitis", "Panniculitis, Lupus Erythematosus", "Lupus Erythematosus Panniculitides", "Panniculitides, Lupus Erythematosus", "Lupus erythematosus profundus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lupus erythematosus panniculitis", "shortest_name_length": 15}
{"curie": "MONDO:0013358", "names": ["SCKL4", "Seckel syndrome 4", "SECKEL SYNDROME 4", "CENPJ Seckel syndrome", "Seckel syndrome type 4", "Seckel syndrome caused by mutation in CENPJ"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Seckel syndrome 4", "shortest_name_length": 5}
{"curie": "MONDO:0012284", "names": ["NEDE", "Nede", "NEPHROPATHY, PROGRESSIVE, WITH DEAFNESS", "nephropathy, progressive, with deafness", "Nephropathy, Progressive, with Deafness", "Alport/focal segmental glomerulosclerosis-like syndrome", "ALPORT/FOCAL SEGMENTAL GLOMERULOSCLEROSIS-LIKE SYNDROME", "Alport Focal Segmental Glomerulosclerosis-Like Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephropathy, progressive, with deafness", "shortest_name_length": 4}
{"curie": "MONDO:0003268", "names": ["mixed glioma", "Mixed Glioma", "Mixed glioma", "Glioma, Mixed", "mixed gliomas", "glioma, mixed", "Mixed Gliomas", "Gliomas, Mixed", "mixed glial tumor", "glial mixed tumor", "Mixed Glial Tumor", "Mixed Glial Neoplasm", "mixed glial neoplasm", "mixed neuroglial tumor", "mixed Neuroglial tumor", "Mixed Neuroglial Tumor", "Mixed glioma (disorder)", "GLIOMA, MIXED, MALIGNANT", "glioma, mixed, malignant", "mixed glioma (diagnosis)", "mixed neuroglial neoplasm", "Mixed Neuroglial Neoplasm", "Mixed glioma (morphologic abnormality)", "mixed glioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed glioma", "shortest_name_length": 12}
{"curie": "MONDO:0019119", "names": ["muscular channelopathy", "muscle tissue channelopathy", "channelopathy of muscle tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular channelopathy", "shortest_name_length": 22}
{"curie": "MONDO:0021020", "names": ["UGT deficiency type 1", "Crigler-Najjar syndrome type 1", "Crigler-Najjar syndrome, type 1", "Crigler-Najjar syndrome, type I", "bilirubin-UGT deficiency type 1", "Crigler Najjar syndrome, type 1", "hyperbilirubinemia, Crigler-Najjar type 1", "hereditary unconjugated hyperbilirubinemia type 1", "bilirubin uridinediphosphate glucuronosyltransferase deficiency type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Crigler-Najjar syndrome type 1", "shortest_name_length": 21}
{"curie": "UMLS:C3272280", "names": ["Idiopathic Primary Ventricular Tachycardia/Ventricular Flutter", "IDIOPATHIC PRIMARY VENTRICULAR TACHYCARDIA/VENTRICULAR FLUTTER", "Idiopathic Primary Ventricular Tachycardia/Ventricular Flutter by EKG Finding", "Idiopathic Primary Ventricular Tachycardia/Ventricular Flutter by ECG Finding"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Idiopathic Primary Ventricular Tachycardia/Ventricular Flutter by ECG Finding", "shortest_name_length": 62}
{"curie": "MONDO:0014902", "names": ["NPCA3", "MST1R nasopharyngeal carcinoma", "susceptibility to nasopharyngeal carcinoma 3", "nasopharyngeal carcinoma, susceptibility to, 3", "NASOPHARYNGEAL CARCINOMA, SUSCEPTIBILITY TO, 3", "nasopharyngeal carcinoma, susceptibility to, type 3", "nasopharyngeal carcinoma caused by mutation in MST1R", "nasopharyngeal carcinoma, susceptibility to, 3; NPCA3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasopharyngeal carcinoma, susceptibility to, 3", "shortest_name_length": 5}
{"curie": "UMLS:C1336094", "names": ["Stage 0 Renal Pelvis Cancer", "Stage 0 Carcinoma of Renal Pelvis", "Stage 0 Renal Pelvis Cancer AJCC v7", "Stage 0 Carcinoma of the Renal Pelvis", "Stage 0 Renal Pelvis Urothelial Carcinoma", "Stage 0 Renal Pelvis Urothelial Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Renal Pelvis Cancer AJCC v7", "shortest_name_length": 27}
{"curie": "MONDO:0020405", "names": ["straddling and/or overriding mitral valve"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "straddling and/or overriding mitral valve", "shortest_name_length": 41}
{"curie": "UMLS:C4055191", "names": ["Rubivirus Associated Congenital Nephrotic Syndrome", "Congenital Nephrotic Syndrome - Rubivirus Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Nephrotic Syndrome - Rubivirus Associated", "shortest_name_length": 50}
{"curie": "MONDO:0010443", "names": ["X-linked atrophic macular degeneration", "macular degeneration, X-linked atrophic", "MACULAR DEGENERATION, ATROPHIC, X-LINKED", "macular degeneration, X-linked atrophic, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macular degeneration, X-linked atrophic", "shortest_name_length": 38}
{"curie": "UMLS:C0344720", "names": ["Left atrium dilated", "Dilated left atrium", "Left atrial dilatation", "Left atrial dilatation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Left atrial dilatation", "shortest_name_length": 19}
{"curie": "MONDO:0004455", "names": ["Classic Mesoblastic Nephroma", "Classic Congenital Mesoblastic Nephroma", "classic congenital mesoblastic nephroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "classic congenital mesoblastic nephroma", "shortest_name_length": 28}
{"curie": "UMLS:C1335463", "names": ["Pre-Malignant Skin Epithelial Lesion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pre-Malignant Skin Epithelial Lesion", "shortest_name_length": 36}
{"curie": "UMLS:C1336426", "names": ["Peripheral T-Cell Lymphoma Stage IV", "Stage IV Peripheral T-cell Lymphoma", "Stage IV Mature T- and NK-Cell Lymphoma", "Ann Arbor Stage IV Mature T- and NK-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage IV Mature T- and NK-Cell Lymphoma", "shortest_name_length": 35}
{"curie": "UMLS:C0494710", "names": ["Cyst;oral", "cyst oral", "oral cyst", "MOUTH CYST", "Velar cyst", "mouth cyst", "Mouth cyst", "cysts oral", "Mouth Cyst", "cyst mouth", "mouth; cyst", "cysts mouth", "cyst; mouth", "Cyst of Mouth", "Oral Cavity Cyst", "cyst; oral cavity", "Cyst of the Mouth", "oral cavity; cyst", "Cyst of Oral Cavity", "mouth cyst (diagnosis)", "Cyst of the Oral Cavity", "Cyst of oral region, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mouth cyst", "shortest_name_length": 9}
{"curie": "MONDO:0024632", "names": ["Defective phagocytic cell opsonization", "defective phagocytic cell opsonization", "Defective phagocytic cell opsonisation", "Defective phagocytic cell opsonization (disorder)", "defective phagocytic cell opsonization (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "defective phagocytic cell opsonization", "shortest_name_length": 38}
{"curie": "MONDO:0006723", "names": ["denture sore mouth", "Denture stomatitis", "denture stomatitis", "Denture sore mouth", "Denture Stomatitis", "Stomatitis, Denture", "Denture Stomatitides", "Stomatitides, Denture", "DS - Denture stomatitis", "sore mouth due to dentures", "Denture stomatitis (disorder)", "sore mouth due to dentures (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "denture stomatitis", "shortest_name_length": 18}
{"curie": "UMLS:C1167779", "names": ["Neutropenic infection", "neutropenic infection", "infection neutropenic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neutropenic infection", "shortest_name_length": 21}
{"curie": "UMLS:C5420299", "names": ["Unresectable Testicular Mesothelioma", "Unresectable Tunica Vaginalis Mesothelioma", "Unresectable Paratesticular Malignant Mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Paratesticular Malignant Mesothelioma", "shortest_name_length": 36}
{"curie": "UMLS:C0862641", "names": ["Stage II Prostate Adenocarcinoma", "Adenocarcinoma of the prostate stage II", "Stage II Prostate Adenocarcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma of the prostate stage II", "shortest_name_length": 32}
{"curie": "UMLS:C0403654", "names": ["bladder outflow obstruction", "Bladder outflow obstruction", "BOO - Bladder outflow obstruction", "Bladder outflow obstruction (disorder)", "bladder outflow obstruction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder outflow obstruction", "shortest_name_length": 27}
{"curie": "MONDO:0005767", "names": ["myonecrosis", "gas gangrene", "GANGRENE GAS", "gangrene gas", "Gas Gangrene", "Gas gangrene", "GANGRENE, GAS", "gangrene; gas", "Gangrene, gas", "Gas Gangrenes", "gas; gangrene", "Gangrene, Gas", "Gangrenes, Gas", "malignant edema", "Malignant edema", "Malignant oedema", "Gas gangrene, NOS", "gangrene due to gas", "Clostridial myositis", "clostridial myositis", "gangrene; gas gangrene", "gas bacillus infection", "Gas bacillus infection", "Gas gangrene (disorder)", "Clostridial myonecrosis", "clostridial myonecrosis", "Clostridium; gas-forming", "gas gangrene (diagnosis)", "myonecrosis; Clostridium", "malignant edema (diagnosis)", "Gas gangrene due to Clostridia", "clostridial myositis (diagnosis)", "Progressive emphysematous necrosis", "Gas bacillus infection or gangrene", "clostridial myonecrosis (diagnosis)", "Gas gangrene due to Clostridia, NOS", "CLOSTRIDIAL MYONECROSIS GAS GANGRENE", "CLOSTRIDIAL MYONECROSIS <GAS GANGRENE>", "Clostridial myositis as a result of gas gangrene"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gas gangrene", "shortest_name_length": 11}
{"curie": "MONDO:0011798", "names": ["HARP SYNDROME", "Harp Syndrome", "harp syndrome", "Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration", "hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration", "HYPOPREBETALIPOPROTEINEMIA, ACANTHOCYTOSIS, RETINITIS PIGMENTOSA, AND PALLIDAL DEGENERATION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration", "shortest_name_length": 13}
{"curie": "MONDO:0021377", "names": ["Hypertrophic Lichen Planus", "lichen planus hypertrophic", "hypertrophic lichen planus", "Hypertrophic lichen planus", "Lichen planus, hypertrophic", "lichen planus hypertrophicus", "lichen; planus, hypertrophic", "Lichen planus hypertrophicus", "Hypertrophic lichen planus (disorder)", "hypertrophic lichen planus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophic lichen planus", "shortest_name_length": 26}
{"curie": "MONDO:0005440", "names": ["Embryonal carcinoma", "embryonal carcinoma", "Embryonal Carcinoma", "Carcinoma, Embryonal", "Embryonal Carcinomas", "Carcinomas, Embryonal", "Embryonal carcinoma NOS", "Embryonal adenocarcinoma", "Embryonal carcinoma, NOS", "Embryonal carcinoma (disorder)", "Carcinoma, Embryonal, Malignant", "embryonal carcinoma (diagnosis)", "CARCINOMA, EMBRYONAL, MALIGNANT", "carcinoma, embryonal, malignant", "Extragonadal Embryonal Carcinoma", "primary extragonadal embryonal carcinoma", "Extragonadal Primary Embryonal Carcinoma", "Extragonadal primary embryonal carcinoma", "Primary Extragonadal Embryonal Carcinoma", "Embryonal carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "embryonal carcinoma", "shortest_name_length": 19}
{"curie": "MONDO:0016729", "names": ["Glioneuronal tumor", "Glioneuronal tumour", "mixed neuronal-glial tumor", "Glioneuronal and Neuronal Tumors", "Neuronal and Glio-Neuronal Tumor", "neuronal and Glio-neuronal tumor", "neuronal and Glio-neuronal neoplasm", "Neuronal and Glio-Neuronal Neoplasm", "neuronal and mixed neuronal-glial tumor", "Neuronal and mixed neuronal-glial tumor", "Neuronal and Mixed Neuronal-Glial Tumor", "Neuronal and mixed neuronal-glial tumour", "neuronal and mixed neuronal-glial tumors", "Neuronal and Mixed Neuronal-Glial Tumors", "Neuronal/glioneuronal neoplasm of the CNS", "Neuronal/glioneuronal neoplasm of the central nervous system", "Neuronal and mixed neuronal-glial tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed neuronal-glial tumor", "shortest_name_length": 18}
{"curie": "UMLS:C1335180", "names": ["Ovarian Soft Tissue Tumor", "Soft Tissue Tumor of Ovary", "Ovarian Soft Tissue Neoplasm", "Soft Tissue Neoplasm of Ovary", "Soft Tissue Tumor of the Ovary", "Soft Tissue Neoplasm of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Soft Tissue Neoplasm", "shortest_name_length": 25}
{"curie": "MONDO:0022949", "names": ["defective apolipoprotein b-100"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "defective apolipoprotein b-100", "shortest_name_length": 30}
{"curie": "MONDO:0004883", "names": ["hereditary choroidal atrophy", "Hereditary choroidal atrophy", "Hereditary choroidal dystrophy", "hereditary choroidal dystrophy", "Hereditary choroidal dystrophies", "choroid; degeneration, hereditary", "degeneration; choroid, hereditary", "Hereditary choroidal dystrophy, NOS", "Hereditary choroidal dystrophy (disorder)", "hereditary choroidal dystrophy (diagnosis)", "Hereditary choroidal dystrophy, unspecified", "Hereditary choroidal dystrophy or atrophy, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary choroidal atrophy", "shortest_name_length": 28}
{"curie": "UMLS:C1516068", "names": ["Astler-Coller C1 Colon Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Astler-Coller C1 Colon Carcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C4744525", "names": ["Third Ventricle Germinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Third Ventricle Germinoma", "shortest_name_length": 25}
{"curie": "MONDO:0002401", "names": ["Malignant Tenosynovial Giant Cell Tumor", "malignant tenosynovial giant cell tumor", "Malignant tenosynovial giant cell tumor", "Malignant Tendon Sheath Giant Cell Tumor", "Malignant tenosynovial giant cell tumour", "malignant tendon sheath giant cell tumor", "tenosynovial giant cell tumor, malignant", "Malignant Giant Cell Tumor of Tendon Sheath", "malignant tendon sheath giant cell neoplasm", "Malignant Tendon Sheath Giant Cell Neoplasm", "malignant giant cell tumor of tendon sheath", "Giant cell tumor of tendon sheath, malignant", "giant cell tumour of tendon sheath, malignant", "Giant cell tumour of tendon sheath, malignant", "Malignant Giant Cell Neoplasm of Tendon Sheath", "malignant giant cell neoplasm of tendon sheath", "Malignant Giant Cell Tumor of the Tendon Sheath", "malignant giant cell tumor of the tendon sheath", "malignant giant cell neoplasm of the tendon sheath", "Malignant Giant Cell Neoplasm of the Tendon Sheath", "malignant Giant cell neoplasm of the Tendon Sheath", "Malignant tenosynovial giant cell tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant tenosynovial giant cell tumor", "shortest_name_length": 39}
{"curie": "MONDO:0008698", "names": ["achalasia", "ACHALASIA", "Achalasia", "cardiospasm", "Achalasia NOS", "Achalasia, NOS", "achalasia of cardia", "Achalasia (finding)", "achalasia (disease)", "esophageal achalasia", "achalasia of esophagus", "hypertensive lower esophageal sphincter", "Hypertensive lower esophageal sphincter", "Hypertensive lower oesophageal sphincter", "Hypertensive lower esophageal sphincter (disorder)", "Lack of reflex relaxation of lower oesophageal sphincter", "lack of reflex relaxation of lower oesophageal sphincter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "achalasia", "shortest_name_length": 9}
{"curie": "MONDO:0017894", "names": ["AML with mutated CEBPA", "AML with Mutated CEBPA", "AML with CEBPA somatic mutations", "acute myeloid Leukemia with mutated CEBPA", "Acute myeloid leukemia with mutated CEBPA", "acute myeloid leukemia with mutated CEBPA", "Acute Myeloid Leukemia with Mutated CEBPA", "Acute Myeloid Leukemia with CEBPA Mutation", "Acute myeloid leukemia with CEBPA somatic mutations", "acute myeloid leukemia with CEBPA somatic mutations", "Acute myeloid leukaemia with CEBPA somatic mutations", "Acute Myeloid Leukemia with Non-Germline Mutated CEBPA", "Non-Familial Acute Myeloid Leukemia with Mutated CEBPA", "non-familial acute myeloid leukemia with mutated CEBPA", "acute myeloid Leukemia with non-germline mutated CEBPA", "leukemia AML with CCAAT/enhancer binding protein alpha somatic mutation", "Acute myeloid leukemia with mutation of CCAAT enhancer binding protein alpha gene", "Acute myeloid leukemia with CCAAT/enhancer binding protein alpha somatic mutation", "Acute myeloid leukaemia with mutation of CCAAT enhancer binding protein alpha gene", "Acute myeloid leukaemia with CCAAT/enhancer binding protein alpha somatic mutation", "Acute myeloid leukemia with mutation of CEBPA (CCAAT enhancer binding protein alpha) gene", "Acute myeloid leukaemia with mutation of CEBPA (CCAAT enhancer binding protein alpha) gene", "Acute myeloid leukemia with CCAAT/enhancer binding protein alpha somatic mutation (disorder)", "Acute myeloid leukemia with CCAAT/enhancer binding protein alpha somatic mutation (diagnosis)", "Acute myeloid leukemia with mutation of CCAAT enhancer binding protein alpha gene (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia with CEBPA somatic mutations", "shortest_name_length": 22}
{"curie": "MONDO:0016073", "names": ["syndromic microphthalmia", "microphthalmia, syndromic", "syndrome associated with microphthalmia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic microphthalmia", "shortest_name_length": 24}
{"curie": "UMLS:C1609516", "names": ["Necrotizing retinitis", "Necrotising retinitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Necrotizing retinitis", "shortest_name_length": 21}
{"curie": "UMLS:C4054398", "names": ["Nephrotic Syndrome - ARHGAP24 Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - ARHGAP24 Associated", "shortest_name_length": 40}
{"curie": "MONDO:0010904", "names": ["SETTING-SUN PHENOMENON, FAMILIAL BENIGN", "Setting-Sun Phenomenon, Familial Benign", "setting-Sun phenomenon, familial benign"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "setting-Sun phenomenon, familial benign", "shortest_name_length": 39}
{"curie": "UMLS:C5417734", "names": ["MBBC", "Mandibular Buccal Bifurcation Cyst"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mandibular Buccal Bifurcation Cyst", "shortest_name_length": 4}
{"curie": "MONDO:0035014", "names": ["primary orthostatic disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary orthostatic disorder", "shortest_name_length": 28}
{"curie": "UMLS:C1335966", "names": ["Simple Endometrial Hyperplasia with Atypia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Simple Endometrial Hyperplasia with Atypia", "shortest_name_length": 42}
{"curie": "UMLS:C1883019", "names": ["Severe Combined Immunodeficiency with Absence of T, Normal B Cells"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Severe Combined Immunodeficiency with Absence of T, Normal B Cells", "shortest_name_length": 66}
{"curie": "MONDO:0014202", "names": ["CILD24", "primary ciliary dyskinesia 24", "CILIARY DYSKINESIA, PRIMARY, 24", "ciliary dyskinesia, primary, 24", "RSPH1 primary ciliary dyskinesia", "primary ciliary dyskinesia type 24", "ciliary dyskinesia, primary, type 24", "primary ciliary dyskinesia 24 without situs inversus", "primary ciliary dyskinesia caused by mutation in RSPH1", "ciliary dyskinesia, primary, 24, without situs inversus", "CILIARY DYSKINESIA, PRIMARY, 24, WITHOUT SITUS INVERSUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia 24", "shortest_name_length": 6}
{"curie": "UMLS:C0332691", "names": ["Scald", "scald", "scalds", "scalded", "scalding", "Burn/scald", "scald burn", "burn scald", "burns scald", "burn scalds", "scalded skin", "burns scalds", "injury scald", "burn scalded", "Burns/scalds", "Scald of skin", "scalding burn", "burns scalding", "Scalding injury", "Scald of skin (disorder)", "scalding burn (diagnosis)", "Scalding injury (morphologic abnormality)", "Injury by scald, undetermined whether accidentally or purposely inflicted"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Scalding injury", "shortest_name_length": 5}
{"curie": "UMLS:C2981707", "names": ["IIB", "Stage IIB Uveal Melanoma", "Stage IIB Uveal Melanoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Uveal Melanoma AJCC v7", "shortest_name_length": 3}
{"curie": "MONDO:0005871", "names": ["roundworm", "Roundworm", "nematodiasis", "Nematodiasis", "nematode infection", "Nematode Infection", "Nematode infection", "Infection, Nematode", "roundworm infection", "Nematode infections", "nematode; infection", "Nematode Infections", "infections nematode", "Roundworm infection", "nematode infections", "infection; nematode", "Round worm infection", "roundworm; infection", "Infections, Nematode", "infestation; nematode", "nematode; infestation", "Nematode infection, NOS", "disease due to nematoda", "Disease due to Nematoda", "Roundworm infection NOS", "Roundworm infection, NOS", "DISEASES DUE TO NEMATODA", "Nematoda infectious disease", "Nematoda disease or disorder", "Nematode infection (disorder)", "nematode infection (diagnosis)", "Nematoda caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nematoda infectious disease", "shortest_name_length": 9}
{"curie": "MONDO:0022602", "names": ["brachydactyly small stature face anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly small stature face anomalies", "shortest_name_length": 42}
{"curie": "MONDO:0006994", "names": ["tarsal tunnel syndrome", "syndrome tarsal tunnel", "Tarsal tunnel syndrome", "Tarsal Tunnel Syndrome", "TARSAL TUNNEL SYNDROME", "tarsal tunnel; syndrome", "Syndrome, Tarsal Tunnel", "Tarsal Tunnel Syndromes", "Tunnel Syndrome, Tarsal", "syndrome; tarsal tunnel", "Syndromes, Tarsal Tunnel", "Tunnel Syndromes, Tarsal", "TTS - Tarsal tunnel syndrome", "Tarsal Tunnel Tibial Neuropathy", "Posterior Tibial Nerve Neuralgia", "Tibial Neuropathy, Tarsal Tunnel", "posterior tibial nerve neuralgia", "Tarsal tunnel syndrome (disorder)", "tarsal tunnel syndrome (diagnosis)", "Tarsal Tunnel Entrapment Neuropathy", "Entrapment Neuropathy, Tarsal Tunnel", "Tarsal tunnel syndrome (ankle condition)", "Tarsal tunnel syndrome, unspecified lower limb", "entrapment; neuropathic, nerve, posterior tibial", "compression; posterior tibial nerve (in tarsal tunnel)", "neuropathy of the posterior tibial nerve and its branches"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tarsal tunnel syndrome", "shortest_name_length": 22}
{"curie": "MONDO:0001950", "names": ["corneal ectasia", "Corneal ectasia", "ectasia; cornea", "ectasia corneal", "cornea; ectasia", "Ectasia of cornea", "Corneal ectasia (disorder)", "corneal ectasia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal ectasia", "shortest_name_length": 15}
{"curie": "MONDO:0004533", "names": ["Perineural Angioma", "perineural angioma", "perineural hemangioma", "Perineural Hemangioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "perineural angioma", "shortest_name_length": 18}
{"curie": "MONDO:0007118", "names": ["ANHD", "ITPR2 anhidrosis", "Dann-Epstein-Sohar syndrome", "DANN-EPSTEIN-SOHAR SYNDROME", "anhidrosis caused by mutation in ITPR2", "isolated anhidrosis with normal sweat glands", "anhidrosis, isolated, with normal sweat glands", "ANHIDROSIS, ISOLATED, WITH NORMAL SWEAT GLANDS", "Isolated generalised anhidrosis with normal sweat glands", "isolated generalized anhidrosis with normal sweat glands", "Isolated generalized anhidrosis with normal sweat glands", "Isolated generalized anhidrosis with normal sweat glands (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated anhidrosis with normal sweat glands", "shortest_name_length": 4}
{"curie": "UMLS:C1334275", "names": ["Invasive Breast Cribriform Carcinoma", "Invasive Cribriform Breast Carcinoma", "Invasive Cribriform Carcinoma of Breast", "Infiltrating Cribriform Breast Carcinoma", "Invasive Breast Cribriform Adenocarcinoma", "Infiltrating Cribriform Carcinoma of Breast", "Invasive Cribriform Carcinoma of the Breast", "Invasive Cribriform Ductal Carcinoma of Breast", "Infiltrating Cribriform Carcinoma of the Breast", "Infiltrating Cribriform Ductal Carcinoma of Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Invasive Breast Cribriform Carcinoma", "shortest_name_length": 36}
{"curie": "UMLS:C0340288", "names": ["Stable Angina", "STABLE ANGINA", "Stable angina", "stable angina", "ANGINA STABLE", "angina stable", "Stable Anginas", "Angina, Stable", "Anginas, Stable", "chronic stable angina", "angina chronic stable", "Stable Angina Pectori", "stable chronic angina", "Chronic Stable Angina", "Angina, Chronic Stable", "Angina Pectori, Stable", "Stable angina pectoris", "Pectori, Stable Angina", "Chronic Stable Anginas", "Stable Angina, Chronic", "Stable Angina Pectoris", "Stable Anginas, Chronic", "Angina Pectoris, Stable", "Anginas, Chronic Stable", "Pectoris, Stable Angina", "Stable angina (disorder)", "stable angina (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stable angina", "shortest_name_length": 13}
{"curie": "UMLS:C0263443", "names": ["Acne pustular", "pustular acne", "acne pustular", "ACNE PUSTULAR", "Pustular acne", "Acne pustulosa", "acne; pustular", "pustular; acne", "Acne, pustular", "Pustular acne (disorder)", "pustular acne (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pustular acne", "shortest_name_length": 13}
{"curie": "MONDO:0018856", "names": ["amyloid lichen", "lichen amyloidosus", "lichen amyloidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lichen amyloidosis", "shortest_name_length": 14}
{"curie": "MONDO:0015967", "names": ["MODY", "Monogenic diabetes", "monogenic diabetes", "Monogenic Diabetes", "rare genetic diabetes mellitus", "Maturity Onset Diabetes of the Young"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "monogenic diabetes", "shortest_name_length": 4}
{"curie": "UMLS:C0017418", "names": ["Genital chancre", "Syphilis genital", "Genital syphilis", "syphilis; genital", "genital; syphilitic", "primary genital syphilis", "Primary genital syphilis", "syphilis primary genital", "syphilis; primary, genital", "Genital syphilis (primary)", "primary; syphilitic, genital", "Primary genital syphilis (disorder)", "primary genital syphilis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary genital syphilis", "shortest_name_length": 15}
{"curie": "UMLS:C4553785", "names": ["Stage 0is Renal Pelvis Cancer", "Stage 0is Renal Pelvis Cancer AJCC v8", "Stage 0is Renal Pelvis Urothelial Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0is Renal Pelvis Cancer AJCC v8", "shortest_name_length": 29}
{"curie": "UMLS:C2981409", "names": ["Stage IA Gastric Gastrointestinal Stromal Tumor", "Stage IA Gastric Gastrointestinal Stromal Tumor AJCC v7", "Stage IA Gastric (Stomach) Gastrointestinal Stromal Tumor (GIST)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Gastric Gastrointestinal Stromal Tumor", "shortest_name_length": 47}
{"curie": "UMLS:C4744989", "names": ["Advanced Small Intestinal Small Cell Carcinoma", "Advanced Small Intestinal Small Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Small Intestinal Small Cell Neuroendocrine Carcinoma", "shortest_name_length": 46}
{"curie": "MONDO:0100050", "names": ["Usher syndrome, type 1D/F", "USH1D/F, CDH23/PCDH15, digenic", "Usher syndrome, type 1D/F, CDH23/PCDH15, digenic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Usher syndrome, type 1D/F", "shortest_name_length": 25}
{"curie": "MONDO:0003192", "names": ["rete ovarii tumor", "tumor of rete ovarii", "rete ovarii neoplasm", "Rete Ovarii Neoplasm", "neoplasm of rete ovarii", "rete ovarii benign neoplasm", "rete ovarii neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rete ovarii neoplasm", "shortest_name_length": 17}
{"curie": "MONDO:0007932", "names": ["ARMD2", "Armd2", "Maculopathy, Age-Related, 2", "MACULOPATHY, AGE-RELATED, 2", "maculopathy, age-related, 2", "Macular Degeneration, Senile", "macular Degeneration, Senile", "MACULAR DEGENERATION, SENILE", "age related macular degeneration 2", "Macular Degeneration, Age-Related, 2", "MACULAR DEGENERATION, AGE-RELATED, 2", "macular degeneration, age-related, 2", "age related macular degeneration type 2", "macular Degeneration, age-related, type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "age related macular degeneration 2", "shortest_name_length": 5}
{"curie": "MONDO:0014888", "names": ["MIRAGE", "mirage", "MIRAGE syndrome", "mirage syndrome", "MIRAGE Syndrome", "MIRAGE SYNDROME", "Myelodysplasia-infection-restriction of growth-adrenal hypoplasia-genital anomalies-enteropathy syndrome", "myelodysplasia-infection-restriction of growth-adrenal hypoplasia-genital anomalies-enteropathy syndrome", "Myelodysplasia, Infection, Restriction of Growth, Adrenal Hypoplasia, Genital Phenotypes, and Enteropathy", "Myelodysplasia-infection-restriction of growth-adrenal hypoplasia-genital phenotypes-enteropathy syndrome", "myelodysplasia, infection, restriction of Growth, adrenal Hypoplasia, genital phenotypes, and enteropathy", "myelodysplasia-infection-restriction of growth-adrenal hypoplasia-genital phenotypes-enteropathy syndrome", "MYELODYSPLASIA, INFECTION, RESTRICTION OF GROWTH, ADRENAL HYPOPLASIA, GENITAL PHENOTYPES, AND ENTEROPATHY", "Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome", "Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital phenotypes, enteropathy syndrome", "MIRAGE (myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy) syndrome", "Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MIRAGE syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C1518728", "names": ["Ovarian Retiform Sertoli-Leydig Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Retiform Sertoli-Leydig Cell Tumor", "shortest_name_length": 42}
{"curie": "MONDO:0012935", "names": ["CLLS4", "Clls4", "leukemia, chronic lymphocytic susceptibility to, 4", "leukemia, chronic lymphocytic, susceptibility to, 4", "LEUKEMIA, CHRONIC LYMPHOCYTIC, SUSCEPTIBILITY TO, 4", "leukemia, chronic lymphocytic, susceptibility to, type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukemia, chronic lymphocytic, susceptibility to, 4", "shortest_name_length": 5}
{"curie": "MONDO:0016054", "names": ["brain malformation", "cerebral malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral malformation", "shortest_name_length": 18}
{"curie": "MONDO:0000075", "names": ["neuronopathy, distal hereditary motor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuronopathy, distal hereditary motor", "shortest_name_length": 37}
{"curie": "UMLS:C4725862", "names": ["Unresectable Dedifferentiated Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Dedifferentiated Liposarcoma", "shortest_name_length": 41}
{"curie": "UMLS:C2751780", "names": ["Retinitis Pigmentosa, Juvenile, SPATA7-Related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retinitis Pigmentosa, Juvenile, SPATA7-Related", "shortest_name_length": 46}
{"curie": "MONDO:0005792", "names": ["herpes stomatitis", "Herpes stomatitis", "STOMATITIS HERPES", "stomatitis; herpes", "herpes; stomatitis", "ORAL HERPES SIMPLEX", "herpes oral simplex", "oral herpes simplex", "oral Herpes simplex", "Herpetic stomatitis", "Herpetic Stomatitis", "herpes simplex oral", "Herpes simplex oral", "herpetic stomatitis", "Oral Herpes Simplex", "Herpes Simplex, Oral", "simplex, oral Herpes", "Herpes simplex, oral", "Stomatitis, Herpetic", "Simplex, Oral Herpes", "Herpes simplex;mouth", "herpetic Stomatitides", "Herpetic Stomatitides", "Stomatitides, Herpetic", "Stomatitides, herpetic", "Simplexvirus stomatitis", "stomatitis; herpesviral", "GINGIVOSTOMATITIS HERPES", "gingivostomatitis; herpes", "herpes; gingivostomatitis", "herpetic Gingivostomatitis", "Herpetic Gingivostomatitis", "HERPETIC GINGIVOSTOMATITIS", "herpetic gingivostomatitis", "Herpetic gingivostomatitis", "Gingivostomatitis, Herpetic", "Gingivostomatitis, herpetic", "herpes simplex in the mouth", "herpetic Gingivostomatitides", "Herpetic Gingivostomatitides", "Gingivostomatitides, herpetic", "Gingivostomatitides, Herpetic", "Simplexvirus caused stomatitis", "Herpes simplex gingivostomatitis", "Primary herpetic gingivostomatitis", "Herpetic gingivostomatitis (disorder)", "herpes simplex virus gingivostomatitis", "Herpes simplex virus gingivostomatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "herpes simplex virus gingivostomatitis", "shortest_name_length": 17}
{"curie": "UMLS:C0854920", "names": ["Relapsed Ureter Cancer", "Ureter cancer recurrent", "recurrent ureter cancer", "Recurrent Ureter Cancer", "Relapsed Ureteral Cancer", "Ureteric cancer recurrent", "Relapsed Cancer of Ureter", "Recurrent Ureter Carcinoma", "Ureteric Cancer, Recurrent", "Relapsed Cancer of the Ureter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Ureter Carcinoma", "shortest_name_length": 22}
{"curie": "MONDO:0001177", "names": ["Anorectal Stenoses", "ANORECTAL STENOSIS", "Anorectal stenosis", "Anorectal Stenosis", "Stenosis, Anorectal", "anorectal stricture", "Anorectal stricture", "ANORECTAL STRICTURE", "Stenoses, Anorectal", "anus; stenosis, and rectum", "anal; stenosis, and rectum", "Stricture of the anorectum", "stenosis of anus and rectum", "Stenosis of rectum and anus", "Stenosis of anus and rectum", "stenosis of rectum and anus", "Anorectal stricture (disorder)", "anorectal stricture (diagnosis)", "Stenosis of rectum and anus (disorder)", "stenosis of anus and rectum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anorectal stricture", "shortest_name_length": 18}
{"curie": "MONDO:0017092", "names": ["Unilateral polymicrogyria", "unilateral polymicrogyria", "Unilateral polymicrogyria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "unilateral polymicrogyria", "shortest_name_length": 25}
{"curie": "MONDO:0010971", "names": ["INFUNDIBULOPELVIC DYSGENESIS", "infundibulopelvic dysgenesis", "Infundibulopelvic dysgenesis", "Infundibulopelvic stenosis multicystic kidney syndrome", "infundibulopelvic stenosis-multicystic kidney syndrome", "Infundibulopelvic stenosis multicystic kidney syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infundibulopelvic stenosis-multicystic kidney syndrome", "shortest_name_length": 28}
{"curie": "UMLS:C5237753", "names": ["Non-Recurrent Lung Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Recurrent Lung Carcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0009766", "names": ["Oculocerebral hypopigmentation syndrome of Preus", "Oculocerebral Hypopigmentation Syndrome of Preus", "OCULOCEREBRAL HYPOPIGMENTATION SYNDROME OF PREUS", "oculocerebral hypopigmentation syndrome of Preus", "oculocerebral hypopigmentation syndrome type Preus", "Oculocerebral hypopigmentation syndrome type Preus", "Oculocerebral hypopigmentation syndrome, Preus type", "Oculocerebral hypopigmentation syndrome of Preus type", "Oculocerebral hypopigmentation syndrome of Preus type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculocerebral hypopigmentation syndrome of Preus", "shortest_name_length": 48}
{"curie": "MONDO:0011851", "names": ["MGR6", "FHM4", "MIGRAINE, FAMILIAL HEMIPLEGIC, 4", "Migraine, Familial Hemiplegic, 4", "migraine, familial hemiplegic, 4", "MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 6", "migraine with or without aura, susceptibility to, 6", "migraine with or without aura, susceptibility to, type 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "migraine with or without aura, susceptibility to, 6", "shortest_name_length": 4}
{"curie": "MONDO:0000972", "names": ["Gallbladder Lipoma", "gallbladder lipoma", "gall bladder lipoma", "lipoma of gallbladder", "Lipoma of Gallbladder", "lipoma of gall bladder", "Lipoma of the gallbladder", "lipoma of the gallbladder", "Lipoma of the Gallbladder", "benign lipoma of gallbladder", "benign lipoma of gallbladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gallbladder lipoma", "shortest_name_length": 18}
{"curie": "UMLS:C0477432", "names": ["Posttraumatic hydrocephalus", "post-traumatic hydrocephalus", "Post-Traumatic Hydrocephalus", "hydrocephalus post-traumatic", "Post Traumatic Hydrocephalus", "Post-traumatic hydrocephalus", "post-traumatic; hydrocephalus", "Hydrocephalus, Post-Traumatic", "hydrocephalus; post-traumatic", "Hydrocephalus following traumatic injury", "post-traumatic hydrocephalus (diagnosis)", "Post-traumatic hydrocephalus, unspecified", "Hydrocephalus following traumatic injury (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post-Traumatic Hydrocephalus", "shortest_name_length": 27}
{"curie": "MONDO:0006222", "names": ["Gastric Choriocarcinoma", "gastric choriocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric choriocarcinoma", "shortest_name_length": 23}
{"curie": "UMLS:C0854193", "names": ["Cognitive deterioration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cognitive deterioration", "shortest_name_length": 23}
{"curie": "MONDO:0014384", "names": ["hypt12", "HYPT12", "Hypt12", "hypotrichosis 12", "HYPOTRICHOSIS 12", "RPL21 hypotrichosis", "hypotrichosis type 12", "hypotrichosis caused by mutation in RPL21"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotrichosis 12", "shortest_name_length": 6}
{"curie": "UMLS:C0751780", "names": ["Biotin-Responsive Encephalopathy", "Biotin Responsive Encephalopathy", "Encephalopathy, Biotin-Responsive", "Biotin-Responsive Encephalopathies", "Encephalopathies, Biotin-Responsive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Biotin-Responsive Encephalopathy", "shortest_name_length": 32}
{"curie": "UMLS:C0752351", "names": ["Embryo Loss"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Embryo Loss", "shortest_name_length": 11}
{"curie": "MONDO:0015698", "names": ["THI", "Newborn gammaglobulin deficiency", "Immunoglobulin maturational delay", "Transient hypogammaglobulinemia of young", "transient hypogammaglobulinemia of infancy", "hypogammaglobulinemia transient of infancy", "Transient hypogammaglobulinemia of infancy", "Transient Hypogammaglobulinemia of Infancy", "Transient hypogammaglobulinaemia of infancy", "THI - Transient hypogammaglobulinemia of infancy", "THI - Transient hypogammaglobulinaemia of infancy", "Transient hypogammaglobulinemia of infancy (disorder)", "transient hypogammaglobulinemia of infancy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transient hypogammaglobulinemia of infancy", "shortest_name_length": 3}
{"curie": "UMLS:C0855114", "names": ["Stage II Diffuse Large B-Cell Lymphoma", "Diffuse Large B-Cell Lymphoma Stage II", "Diffuse large B-cell lymphoma stage II", "Ann Arbor Stage II Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Diffuse Large B-Cell Lymphoma", "shortest_name_length": 38}
{"curie": "UMLS:C4683784", "names": ["RISS Stage II Plasma Cell Myeloma", "Revised International Staging System Stage II Plasma Cell Myeloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "RISS Stage II Plasma Cell Myeloma", "shortest_name_length": 33}
{"curie": "MONDO:0000344", "names": ["Ross river fever", "Ross River fever", "Ross River virus disease", "Ross River virus infectious disease", "Ross River virus disease or disorder", "Ross River virus caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ross river fever", "shortest_name_length": 16}
{"curie": "UMLS:C0686651", "names": ["lymph node neoplasm malignant secondary mediastinal", "Secondary malignant neoplasm of mediastinal lymph nodes", "Metastatic malignant neoplasm to mediastinal lymph nodes", "Metastatic malignant neoplasm of mediastinal lymph nodes", "metastasis of malignant neoplasm to mediastinal lymph nodes", "Metastatic Malignant Neoplasm in the Mediastinal Lymph Nodes", "malignant neoplasm metastasis to the mediastinal lymph nodes", "Metastatic malignant neoplasm to mediastinal lymph nodes (disorder)", "Secondary malignant neoplasm of mediastinal lymph nodes (diagnosis)", "metastasis of malignant neoplasm to mediastinal lymph nodes (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to mediastinal lymph nodes", "shortest_name_length": 51}
{"curie": "UMLS:C0206676", "names": ["Pulmonary adenomatosis", "Pulmonary Adenomatosis", "Pulmonary Adenomatoses", "pulmonary; adenomatosis", "Adenomatoses, Pulmonary", "Adenomatosis, Pulmonary", "adenomatosis; pulmonary", "Pulmonary adenomatosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenomatosis, Pulmonary", "shortest_name_length": 22}
{"curie": "MONDO:0009056", "names": ["CVG/MR", "cutis verticis gyrata and mental retardation", "CUTIS VERTICIS GYRATA AND MENTAL RETARDATION", "cutis verticis gyrata and intellectual disability", "cutis verticis gyrata-intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutis verticis gyrata and intellectual disability", "shortest_name_length": 6}
{"curie": "MONDO:0015311", "names": ["autism with port-wine stain", "autism-facial port-wine stain syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autism-facial port-wine stain syndrome", "shortest_name_length": 27}
{"curie": "UMLS:C4553751", "names": ["Stage IV Primary Peritoneal Cancer", "Stage IV Primary Peritoneal Cancer AJCC v8", "Stage IV Primary Peritoneal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Primary Peritoneal Cancer AJCC v8", "shortest_name_length": 34}
{"curie": "UMLS:C0235487", "names": ["EMBOLISM LIMB", "Embolism limb"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Embolism limb", "shortest_name_length": 13}
{"curie": "MONDO:0011199", "names": ["Nephropathy, Progressive Tubulointerstitial, with Cholestatic Liver Disease", "NEPHROPATHY, PROGRESSIVE TUBULOINTERSTITIAL, WITH CHOLESTATIC LIVER DISEASE", "nephropathy, progressive tubulointerstitial, with cholestatic liver disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephropathy, progressive tubulointerstitial, with cholestatic liver disease", "shortest_name_length": 75}
{"curie": "UMLS:C2931223", "names": ["Thiopurines, poor metabolism of", "6 alpha mercaptopurine sensitivity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "6 alpha mercaptopurine sensitivity", "shortest_name_length": 31}
{"curie": "UMLS:C3272766", "names": ["High Grade Appendix Mucinous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Appendix Mucinous Adenocarcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0022337", "names": ["AIDS dysmorphic syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS dysmorphic syndrome", "shortest_name_length": 24}
{"curie": "MONDO:0008291", "names": ["PPPD", "PPPD1", "POROK2", "Type 2 Punctate PPK", "Porokeratosis of Mantoux", "Palmoplantar Porokeratosis", "Porokeratosis, Palmoplantar", "Keratoderma Palmoplantar, Punctate Type 2", "Palmar, plantar and disseminated porokeratosis", "palmar, plantar and disseminated porokeratosis", "porokeratosis palmaris Et plantaris disseminata", "Porokeratosis plantaris palmaris et disseminata", "Porokeratosis Palmaris et Plantaris Disseminata", "porokeratosis palmaris et plantaris disseminata", "POROKERATOSIS PALMARIS ET PLANTARIS DISSEMINATA", "Porokeratosis Plantaris Palmaris et Disseminata", "porokeratosis plantaris palmaris et disseminata", "POROKERATOSIS PLANTARIS PALMARIS ET DISSEMINATA", "POROKERATOSIS, PALMAR, PLANTAR, AND DISSEMINATED", "porokeratosis, palmar, plantar, and disseminated", "Porokeratosis Plantaris, Palmaris, Et Disseminata", "porokeratosis 2, palmar, plantar, and disseminated", "Porokeratosis, Palmar, Plantar, And Disseminated 1", "POROKERATOSIS, PALMAR, PLANTAR, AND DISSEMINATED, 1", "porokeratosis, palmar, plantar, and disseminated, 1", "POROKERATOSIS 2, PALMAR, PLANTAR, AND DISSEMINATED TYPE", "porokeratosis 2, palmar, plantar, and disseminated type", "Porokeratosis plantaris palmaris et disseminata (disorder)", "porokeratosis palmaris et plantaris disseminata (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "porokeratosis plantaris palmaris et disseminata", "shortest_name_length": 4}
{"curie": "UMLS:C0473508", "names": ["Late Postpartum Hemorrhage", "Delayed Postpartum Hemorrhage", "Delayed postpartum hemorrhage", "Hemorrhage, Delayed Postpartum", "postpartum; delayed hemorrhage", "Delayed postpartum haemorrhage", "Postpartum Hemorrhage, Delayed", "delayed; hemorrhage postpartum", "hemorrhage; delayed postpartum", "Secondary Postpartum Hemorrhage", "Secondary postpartum hemorrhage", "Secondary postpartum haemorrhage", "Postpartum hemorrhage (secondary)", "Postpartum haemorrhage (secondary)", "delayed / secondary postpartum hemorrhage", "postpartum hemorrhage delayed or secondary", "Delayed or secondary postpartum hemorrhage", "delayed or secondary postpartum hemorrhage", "Delayed and secondary postpartum hemorrhage", "Delayed or secondary postpartum haemorrhage", "hemorrhage; postpartum, delayed or secondary", "Delayed and secondary postpartum haemorrhage", "postpartum; hemorrhage, delayed or secondary", "Delayed AND/OR secondary postpartum hemorrhage", "Postpartum hemorrhage, delayed AND/OR secondary", "Delayed AND/OR secondary postpartum haemorrhage", "Postpartum haemorrhage, delayed AND/OR secondary", "delayed or secondary postpartum hemorrhage (diagnosis)", "Hemorrhage after the first 24 hours following delivery", "Delayed and secondary postpartum hemorrhage, postpartum", "Postpartum hemorrhage specified as delayed or secondary", "Postpartum haemorrhage specified as delayed or secondary", "Delayed AND/OR secondary postpartum hemorrhage (disorder)", "Hemorrhage after first 24 hours following delivery of placenta", "Haemorrhage after first 24 hours following delivery of placenta", "Delayed and secondary postpartum hemorrhage, unspecified as to episode of care", "Delayed and secondary postpartum hemorrhage, postpartum condition or complication", "Delayed and secondary postpartum hemorrhage, unspecified as to episode of care or not applicable"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Delayed Postpartum Hemorrhage", "shortest_name_length": 26}
{"curie": "UMLS:C4086169", "names": ["Childhood Pineal Parenchymal Tumor of Intermediate Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Pineal Parenchymal Tumor of Intermediate Differentiation", "shortest_name_length": 66}
{"curie": "MONDO:0015727", "names": ["Mosaic trisomy 15", "mosaic trisomy 15", "Trisomy 15 mosaicism", "trisomy 15 mosaicism", "Mosaic trisomy type 15", "Uniparental disomy of 15", "Mosaic trisomy 15 syndrome", "Mosaic trisomy chromosome 15", "Chromosome 15, trisomy mosaicism", "chromosome 15, trisomy mosaicism", "Mosaic trisomy 15 syndrome (disorder)", "Mosaic trisomy 15 syndrome (diagnosis)", "anomaly of chromosome pair mosaic trisomy 15 syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mosaic trisomy 15", "shortest_name_length": 17}
{"curie": "MONDO:0017683", "names": ["methylcobalamin deficiency type cblDv1", "functional methionine synthase deficiency type cblDv1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "methylcobalamin deficiency type cblDv1", "shortest_name_length": 38}
{"curie": "MONDO:0010094", "names": ["SCT", "SCT Syndrome", "Synspondylism", "Synspondylism congenital", "Congenital Synspondylism", "Congenital synspondylism", "congenital synspondylism", "SYNSPONDYLISM, CONGENITAL", "Synspondylism, congenital", "spondylocarpotarsal syndrome", "Spondylocarpotarsal Syndrome", "SPONDYLOCARPOTARSAL SYNDROME", "spondylocarpotarsal synostosis", "Spondylocarpotarsal synostosis", "vertebral fusion with carpal coalition", "VERTEBRAL FUSION WITH CARPAL COALITION", "Vertebral fusion with carpal coalition", "spondylocarpotarsal synostosis syndrome", "Spondylocarpotarsal synostosis syndrome", "SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME", "Spondylocarpotarsal synostosis syndrome (disorder)", "Congenital Scoliosis with Unilateral Unsegmented Bar", "Congenital scoliosis with unilateral unsegmented bar", "congenital scoliosis with unilateral unsegmented bar", "scoliosis, congenital with unilateral unsegmented bar", "SCOLIOSIS, CONGENITAL, WITH UNILATERAL UNSEGMENTED BAR", "scoliosis, congenital, with unilateral unsegmented Bar", "Scoliosis, congenital, with unilateral unsegmented bar"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondylocarpotarsal synostosis syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0032639", "names": ["DFNB112", "autosomal recessive deafness 112", "deafness, autosomal recessive 112", "DEAFNESS, AUTOSOMAL RECESSIVE 112", "hearing loss, autosomal recessive 112", "autosomal recessive nonsyndromic deafness 112"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal recessive 112", "shortest_name_length": 7}
{"curie": "MONDO:0014707", "names": ["dup(14)q(32)", "trisomy 14q32", "14q32 duplication syndrome", "chromosome 14q32 DUPLICATION syndrome, 700-KB", "myeloproliferative neoplasms, familial, susceptibility to", "predisposition to adult-onset myeloproliferative neoplasm due to 14q32 duplication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "14q32 duplication syndrome", "shortest_name_length": 12}
{"curie": "UMLS:C1335677", "names": ["Rectal Adenoma with Severe Dysplasia", "Rectal Adenoma with Marked Dysplasia", "Adenoma of Rectum with Marked Dysplasia", "Adenoma of the Rectum with Marked Dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rectal Adenoma with Severe Dysplasia", "shortest_name_length": 36}
{"curie": "MONDO:0023178", "names": ["fragile X syndrome type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fragile X syndrome type 1", "shortest_name_length": 25}
{"curie": "MONDO:0020750", "names": ["PLOSL2", "polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2", "POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2", "shortest_name_length": 6}
{"curie": "MONDO:0000461", "names": ["B7 deficiency", "Biotin deficiency", "deficiency biotin", "biotin deficiency", "biotin; deficiency", "Disorder of biotin", "deficiency; biotin", "Deficiency of biotin", "vitamine B7 deficiency", "Biotin deficiency disease", "biotin deficiency disease", "Biotin deficiency (disorder)", "biotin deficiency (diagnosis)", "nutritional biotin deficiency", "deficiency; vitamin, H (biotin)", "vitamin; deficiency, H (biotin)", "Deficiency of biotin (disorder)", "Biotin deficiency disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nutritional biotin deficiency", "shortest_name_length": 13}
{"curie": "UMLS:C4727149", "names": ["Relapsed Severe Aplastic Anemia", "Recurrent Severe Aplastic Anemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Severe Aplastic Anemia", "shortest_name_length": 31}
{"curie": "MONDO:0000307", "names": ["Ichthyosporea infectious disease", "Ichthyosporea disease or disorder", "Ichthyosporea caused disease or disorder", "parasitic Ichthyosporea infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parasitic Ichthyosporea infectious disease", "shortest_name_length": 32}
{"curie": "MONDO:0003874", "names": ["ovary papillary carcinoma", "Serous Surface Papillary Carcinoma of Ovary", "serous Surface Papillary carcinoma of Ovary", "serous surface papillary carcinoma of ovary", "Serous Surface Papillary Carcinoma of the Ovary", "serous surface papillary carcinoma of the ovary", "Ovarian Serous Surface Papillary Adenocarcinoma", "ovarian serous surface papillary adenocarcinoma", "serous surface papillary carcinoma of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian serous surface papillary adenocarcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0009802", "names": ["Danks Mayne Kozlowski precocious osteodysplasty", "osteodysplasty precocious of Danks Mayne and Kozlowski", "OSTEODYSPLASTY, PRECOCIOUS, OF DANKS, MAYNE, AND KOZLOWSKI", "osteodysplasty, precocious, of Danks, Mayne, and Kozlowski", "Osteodysplasty, Precocious, Of Danks, Mayne, And Kozlowski"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteodysplasty, precocious, of Danks, Mayne, and Kozlowski", "shortest_name_length": 47}
{"curie": "UMLS:C1336729", "names": ["Testicular Teratoma with Somatic-Type Malignancy", "Testicular Teratoma with Non-Germ Cell Malignancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular Teratoma with Somatic-Type Malignancy", "shortest_name_length": 48}
{"curie": "MONDO:0012978", "names": ["CILD11", "primary ciliary dyskinesia 11", "CILIARY DYSKINESIA, PRIMARY, 11", "ciliary dyskinesia, primary, 11", "Ciliary Dyskinesia, Primary, 11", "RSPH4A primary ciliary dyskinesia", "primary ciliary dyskinesia type 11", "ciliary dyskinesia, primary, type 11", "primary ciliary dyskinesia 11 without situs inversus", "primary ciliary dyskinesia caused by mutation in RSPH4A", "ciliary dyskinesia, primary, 11, without situs inversus", "CILIARY DYSKINESIA, PRIMARY, 11, WITHOUT SITUS INVERSUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia 11", "shortest_name_length": 6}
{"curie": "MONDO:0018000", "names": ["thrombocythemia with distal limb defects", "familial thrombocytosis with transverse limb defect", "hereditary thrombocytosis with transverse limb defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary thrombocytosis with transverse limb defect", "shortest_name_length": 40}
{"curie": "MONDO:0012260", "names": ["CATCN1", "CTRCT35", "CATARACT 35", "cataract 35", "cataract type 35", "cataract 35, congenital nuclear", "autosomal recessive congenital nuclear cataract 1", "CATARACT, CONGENITAL NUCLEAR, AUTOSOMAL RECESSIVE 1", "Cataract, Congenital Nuclear, Autosomal Recessive 1", "cataract, congenital nuclear, autosomal recessive 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 35", "shortest_name_length": 6}
{"curie": "MONDO:0700183", "names": ["feline reticulum cell sarcoma", "Feline Reticulum Cell Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "feline reticulum cell sarcoma", "shortest_name_length": 29}
{"curie": "UMLS:C0238158", "names": ["TRANSFUSION SIDEROSIS", "HEMOSIDEROSIS, EXOGENOUS", "secondary hemochromatosis", "Secondary hemochromatosis", "Secondary Hemochromatosis", "HEMOCHROMATOSIS, EXOGENOUS", "HEMOCHROMATOSIS, SECONDARY", "Secondary haemochromatosis", "Secondary hemochromatosis, NOS", "Secondary hemochromatosis (disorder)", "secondary hemochromatosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary hemochromatosis", "shortest_name_length": 21}
{"curie": "UMLS:C0162279", "names": ["detachment; choroid", "choroid; detachment", "DETACHMENT CHORIDAL", "Detachment choroidal", "CHOROIDAL DETACHMENT", "choroidal detachment", "Choroidal Detachment", "Choroidal detachment", "Choroidal Detachments", "Ciliochoroidal Detachment", "Choroidal detachment, NOS", "Ciliochoroidal Detachments", "Choroidal detachment (disorder)", "choroidal detachment (diagnosis)", "Unspecified choroidal detachment", "Choroidal detachment, unspecified", "choroidal detachment (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Choroidal Detachment", "shortest_name_length": 19}
{"curie": "MONDO:0009554", "names": ["3MC3", "3MC SYNDROME 3", "3MC syndrome 3", "Malpuech syndrome", "3Mc syndrome type 3", "3MC syndrome type 3", "COLEC10 3MC syndrome", "Malpuech facial clefting syndrome", "Malpuech Facial clefting syndrome", "Facial clefting syndrome, Gypsy type", "facial clefting syndrome, Gypsy type", "FACIAL CLEFTING SYNDROME, GYPSY TYPE", "3MC syndrome caused by mutation in COLEC10", "Malpuech Facial clefting syndrome, formerly", "MALPUECH FACIAL CLEFTING SYNDROME, FORMERLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "3MC syndrome 3", "shortest_name_length": 4}
{"curie": "UMLS:C0236003", "names": ["mucosal swelling", "MUCOSAL SWELLING", "Mucosal swelling", "Mucosal swelling NOS", "mucous membrane swelling", "Mucous membrane swelling", "Mucous membrane swelling (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mucous membrane swelling", "shortest_name_length": 16}
{"curie": "UMLS:C2986684", "names": ["Stage II AIDS-Related Lymphoma", "stage II AIDS-related lymphoma", "Ann Arbor Stage II AIDS-Related Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage II AIDS-Related Lymphoma", "shortest_name_length": 30}
{"curie": "MONDO:0021750", "names": ["Pyonephrosis", "pyonephrosis", "Pyonephrosis NOS", "Infected Hydronephrosis", "Pyonephrosis (disorder)", "Hydronephrosis, Infected", "pyonephrosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyonephrosis", "shortest_name_length": 12}
{"curie": "UMLS:C1335153", "names": ["Ovarian Carcinoid Tumor", "Carcinoid Tumor of Ovary", "Carcinoid tumor of the ovary", "Carcinoid Tumor of the Ovary", "Carcinoid tumour of the ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Carcinoid Tumor", "shortest_name_length": 23}
{"curie": "UMLS:C2827494", "names": ["Beta-Methylcrotonylglycinuria", "Beta-methylcrotonyglycinuria (Types I or II)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Beta-Methylcrotonylglycinuria", "shortest_name_length": 29}
{"curie": "MONDO:0002971", "names": ["amelanotic melanoma", "Amelanotic Melanoma", "Amelanotic melanoma", "Melanoma, Amelanotic", "amelanotic melanomas", "Amelanotic Melanomas", "melanomas, amelanotic", "Melanomas, Amelanotic", "melanoma, amelanotic, malignant", "MELANOMA, AMELANOTIC, MALIGNANT", "amelanotic melanoma (morphologic abnormality)", "Amelanotic melanoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amelanotic melanoma", "shortest_name_length": 19}
{"curie": "UMLS:C0750151", "names": ["Sickle Cell Crisis", "VASO OCCLUSIVE CRISIS", "Vaso-occlusive crisis", "Vaso-Occlusive Crisis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaso-Occlusive Crisis", "shortest_name_length": 18}
{"curie": "MONDO:0004156", "names": ["pancreatic colloid Cystadencarcinoma", "Pancreatic Colloid Cystadencarcinoma", "Colloid Cystadencarcinoma of Pancreas", "colloid Cystadencarcinoma of pancreas", "pancreatic colloid cystadenocarcinoma", "Pancreatic mucinous cystadenocarcinoma", "mucinous Cystadencarcinoma of pancreas", "pancreatic mucinous cystadenocarcinoma", "pancreatic colloidal Cystadencarcinoma", "Mucinous Cystadencarcinoma of Pancreas", "Pancreatic Mucinous Cystadenocarcinoma", "Pancreatic Colloidal Cystadencarcinoma", "Mucinous cystadenocarcinoma of pancreas", "colloidal Cystadencarcinoma of pancreas", "Colloidal Cystadencarcinoma of Pancreas", "mucinous cystadenocarcinoma of pancreas", "Colloid Cystadencarcinoma of the Pancreas", "colloid Cystadencarcinoma of the pancreas", "mucinous Cystadencarcinoma of the pancreas", "Mucinous Cystadencarcinoma of the Pancreas", "Mucinous cystadenocarcinoma of the pancreas", "Colloidal Cystadencarcinoma of the Pancreas", "colloidal Cystadencarcinoma of the pancreas", "Mucinous cystadenocarcinoma of pancreas (disorder)", "mucinous cystadenocarcinoma of pancreas (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic mucinous cystadenocarcinoma", "shortest_name_length": 36}
{"curie": "UMLS:C0005658", "names": ["bite", "BITE", "Bite", "Bites", "bites", "biting", "Biting", "Bite NOS", "Bite, NOS", "bite wound", "Bite wound", "bite injury", "Bite Injury", "bite wounds", "Bite - wound", "bite - wound", "Bite - wound (disorder)", "bite (see also by location)", "Bite (morphologic abnormality)", "bite injury (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bite injury", "shortest_name_length": 4}
{"curie": "MONDO:0020363", "names": ["honey-droplet corneal dystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "honey-droplet corneal dystrophy", "shortest_name_length": 31}
{"curie": "MONDO:0007467", "names": ["REPETITIVE SEQUENCE DNA", "repetitive sequence DNA", "DNA, LOW-REPETITIVE SEQUENCES OF", "DNA, low-repetitive sequences of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DNA, low-repetitive sequences of", "shortest_name_length": 23}
{"curie": "EFO:0009704", "names": ["radiation-induced brain injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radiation-induced brain injury", "shortest_name_length": 30}
{"curie": "MONDO:0018680", "names": ["Spiegler-Fendt", "Lymphocytoma cutis", "LYMPHOCYTOMA CUTIS", "lymphocytoma cutis", "Lymphocytoma Cutis", "Skin pseudolymphoma", "SPIEGLER-FENDT SARCOID", "Spiegler-Fendt sarcoid", "pseudolymphoma cutaneous", "Cutaneous pseudolymphoma", "cutaneous pseudolymphoma", "Cutaneous Pseudolymphoma", "Benign lymphocytoma cutis", "pseudolymphoma of Spiegler", "Pseudolymphoma of Spiegler", "lymphadenosis Benigna cutis", "Lymphadenosis Benigna Cutis", "Cutaneous lymphoid hyperplasia", "cutaneous lymphoid hyperplasia", "Pseudolymphoma of Spiegler-Fendt", "Cutaneous pseudolymphoma (disorder)", "Cutaneous pseudolymphoma (diagnosis)", "Benign cutaneous lymphoid hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous pseudolymphoma", "shortest_name_length": 14}
{"curie": "UMLS:C1706835", "names": ["Tubular carcinoid", "Appendix Tubular Carcinoid", "Appendix Tubular Carcinoid Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Appendix Tubular Carcinoid", "shortest_name_length": 17}
{"curie": "MONDO:0017123", "names": ["ARCS", "ARC SYNDROME", "ARC syndrome", "Arthrogryposis-renal dysfunction-cholestasis", "arthrogryposis-renal dysfunction-cholestasis", "arthrogryposis - renal dysfunction - cholestasis", "ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS", "arthrogryposis, renal dysfunction, and cholestasis", "arthrogryposis renal dysfunction cholestasis syndrome", "Arthrogryposis-renal dysfunction-cholestasis syndrome", "arthrogryposis-renal dysfunction-cholestasis syndrome", "Arthrogryposis renal dysfunction cholestasis syndrome", "ARC (arthrogryposis, renal dysfunction, cholestasis) syndrome", "Arthrogryposis with renal dysfunction and cholestasis syndrome", "arthrogryposis, renal dysfunction and cholestasis (ARC) syndrome", "Arthrogryposis, renal dysfunction and cholestasis (ARC) syndrome", "arthrogryposis multiplex congenita, renal dysfunction, and cholestasis", "Arthrogryposis with renal dysfunction and cholestasis syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis-renal dysfunction-cholestasis syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0010952", "names": ["HHCS", "HRFTC", "Bonneau-Beaumont Syndrome", "Bonneau-Beaumont syndrome", "hyperferritinemia-cataract syndrome", "hyperferritinemia cataract syndrome", "cataract-hyperferritinemia syndrome", "Hyperferritinemia-Cataract Syndrome", "Hyperferritinemia cataract syndrome", "HYPERFERRITINEMIA-CATARACT SYNDROME", "Dominant hyperferritinemia and cataract", "hyperferritinemia with or without cataract", "HYPERFERRITINEMIA WITH OR WITHOUT CATARACT", "hereditary hyperferritinemia cataract syndrome", "hereditary hyperferritinemia-cataract syndrome", "Hyperferritinemia cataract syndrome (disorder)", "Hereditary hyperferritinemia-cataract syndrome", "hereditary hyperferritinemia with congenital cataracts", "Hereditary hyperferritinemia with congenital cataracts", "Hereditary Hyperferritinemia with Congenital Cataracts", "Hyperferritinemia, hereditary, with congenital cataracts", "hyperferritinemia, hereditary, with congenital cataracts", "HYPERFERRITINEMIA, HEREDITARY, WITH CONGENITAL CATARACTS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary hyperferritinemia with congenital cataracts", "shortest_name_length": 4}
{"curie": "MONDO:0010955", "names": ["Ectodermal dysplasia mental retardation syndactyly", "ectodermal dysplasia mental retardation syndactyly", "ectodermal dysplasia intellectual disability syndactyly", "Ectodermal dysplasia with mental retardation and syndactyly", "ectodermal dysplasia with mental retardation and syndactyly", "ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY", "ectodermal dysplasia with intellectual disability and syndactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia with intellectual disability and syndactyly", "shortest_name_length": 50}
{"curie": "UMLS:C4525862", "names": ["Stage IIB Rectal Neuroendocrine Tumor", "Stage IIB Rectal Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Rectal Neuroendocrine Tumor AJCC v8", "shortest_name_length": 37}
{"curie": "MONDO:0018454", "names": ["genetic dysostosis", "dysostosis of genetic origin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dysostosis of genetic origin", "shortest_name_length": 18}
{"curie": "MONDO:0018385", "names": ["genetic osteochondrosis", "osteochondrosis of genetic origin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteochondrosis of genetic origin", "shortest_name_length": 23}
{"curie": "MONDO:0001129", "names": ["Nasal Cavity Olfactory Neuroblastoma", "nasal cavity olfactory neuroblastoma", "olfactory neuroblastoma of nasal cavity", "Olfactory Neuroblastoma of Nasal Cavity", "Olfactory neuroblastoma of the nasal cavity", "olfactory neuroblastoma of the nasal cavity", "Olfactory Neuroblastoma of the Nasal Cavity", "olfactory neuroblastoma of nasal cavity (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasal cavity olfactory neuroblastoma", "shortest_name_length": 36}
{"curie": "UMLS:C0333895", "names": ["Suspect cell present", "Atypia suspicious for malignancy", "Atypia Suspicious for Malignancy", "Atypia, suspicious for malignancy", "Atypia suspicious for malignancy (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypia suspicious for malignancy", "shortest_name_length": 20}
{"curie": "MONDO:0044682", "names": ["MYBPC1-related autosomal recessive non-lethal AMC syndrome", "MYBPC1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MYBPC1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome", "shortest_name_length": 58}
{"curie": "MONDO:0005399", "names": ["Venous thromboembolism", "venous thromboembolism", "VENOUS THROMBOEMBOLISM", "Venous Thromboembolism", "Thromboembolism, Venous"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "venous thromboembolism", "shortest_name_length": 22}
{"curie": "MONDO:0020354", "names": ["Fundus coloboma", "fundus coloboma", "retinal coloboma", "Choroid coloboma", "coloboma; fundus", "fundus; coloboma", "CHOROID COLOBOMA", "Coloboma, choroid", "choroidal coloboma", "Coloboma of retina", "Choroidal coloboma", "Coloboma of fundus", "Coloboma, choroidal", "Coloboma of choroid", "Chorioretinal coloboma", "Coloboma of the fundus", "Chorioretinal colobomas", "Coloboma, chorioretinal", "retinochoroidal coloboma", "Choroidoretinal coloboma", "Retinochoroidal coloboma", "Coloboma, retinochoroidal", "Fundus coloboma (disorder)", "fundus coloboma (diagnosis)", "Congenital coloboma of retina", "Coloboma of choroid (disorder)", "coloboma of choroid and retina", "Birth defect that causes a hole in the innermost layer at the back of the eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coloboma of choroid and retina", "shortest_name_length": 15}
{"curie": "MONDO:0042975", "names": ["Recessive pseudoachondroplasia", "recessive pseudoachondroplasia", "pseudoachondroplastic dysplasia 2", "Pseudoachondroplastic dysplasia 2", "Spondyloepiphyseal dysplasia pseudoachondroplastic 2", "spondyloepiphyseal dysplasia pseudoachondroplastic 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudoachondroplastic dysplasia 2", "shortest_name_length": 30}
{"curie": "MONDO:0008802", "names": ["antithrombin, familial hemorrhagic diathesis due to", "Antithrombin, Familial Hemorrhagic Diathesis due to", "ANTITHROMBIN, FAMILIAL HEMORRHAGIC DIATHESIS DUE TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "antithrombin, familial hemorrhagic diathesis due to", "shortest_name_length": 51}
{"curie": "UMLS:C4683016", "names": ["Stage IIB Eyelid Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Eyelid Carcinoma AJCC v8", "shortest_name_length": 34}
{"curie": "MONDO:0001999", "names": ["primary pulmonary hypertension", "pulmonary hypertension, primary", "Idiopathic pulmonary arterial hypertension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary pulmonary hypertension", "shortest_name_length": 30}
{"curie": "MONDO:0001183", "names": ["Contact lens corneal edema", "contact lens corneal edema", "Contact lens corneal oedema", "Corneal edema due to contact lens", "contact lens-induced corneal edema", "Corneal oedema due to contact lens", "Corneal edema caused by contact lens", "Corneal oedema caused by contact lens", "Contact lens-induced central corneal edema", "Contact lens-induced central corneal oedema", "Corneal edema due to wearing of contact lenses", "contact lens-induced corneal edema (diagnosis)", "Corneal oedema due to wearing of contact lenses", "Corneal edema caused by wearing of contact lenses", "Corneal oedema caused by wearing of contact lenses", "Corneal edema caused by wearing of contact lenses (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "contact lens corneal edema", "shortest_name_length": 26}
{"curie": "MONDO:0004852", "names": ["Gonococcal keratitis", "gonococcal keratitis", "Keratitis blennorrhagica", "Gonococcal keratitis (disorder)", "gonococcal keratitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gonococcal keratitis", "shortest_name_length": 20}
{"curie": "MONDO:0800118", "names": ["visceral botryomycosis", "pulmonary botromycosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "visceral botryomycosis", "shortest_name_length": 22}
{"curie": "UMLS:C0347176", "names": ["Stage 0 Fallopian Tube Cancer", "Tubal Intraepithelial Carcinoma", "Fallopian Tube Carcinoma in Situ", "Carcinoma in situ of fallopian tube", "carcinoma in situ of fallopian tube", "Stage 0 Fallopian Tube Cancer AJCC v7", "Carcinoma in situ of fallopian tube (disorder)", "carcinoma in situ of fallopian tube (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carcinoma in situ of fallopian tube", "shortest_name_length": 29}
{"curie": "UMLS:C5237460", "names": ["Recurrent Transformed T-cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Transformed T-cell Non-Hodgkin Lymphoma", "shortest_name_length": 49}
{"curie": "MONDO:0037807", "names": ["glycerol metabolism disease", "disorders glycerol metabolism", "Disorder of glycerol metabolism", "disorder of glycerol metabolism", "glycerol metabolic process disease", "disorder of glycerol metabolic process", "Disorder of glycerol metabolism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycerol metabolism disease", "shortest_name_length": 27}
{"curie": "MONDO:0002110", "names": ["Adrenal Rest Tumor", "Adrenal rest tumor", "adrenal rest tumor", "Rest Tumor, Adrenal", "Adrenal rest tumour", "Adrenal Rest Tumors", "Tumor, Adrenal Rest", "adrenal rest tumour", "Rest Tumors, Adrenal", "Tumors, Adrenal Rest", "adrenal rest neoplasm", "Adrenal Rest Neoplasm", "Adrenal Rest neoplasm", "adrenal benign rest tumor", "Adrenal Cortical Rest Tumor", "adrenal benign rest tumor (diagnosis)", "Adrenal rest tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adrenal rest tumor", "shortest_name_length": 18}
{"curie": "UMLS:C0205651", "names": ["Trabecular Adenoma", "Trabecular adenoma", "Trabecular Adenomas", "Adenoma, Trabecular", "Adenomas, Trabecular", "Trabecular adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenoma, Trabecular", "shortest_name_length": 18}
{"curie": "MONDO:0011354", "names": ["SITUS INVERSUS TOTALIS WITH CYSTIC DYSPLASIA OF KIDNEYS AND PANCREAS", "situs inversus totalis with cystic dysplasia of kidneys and pancreas", "Situs inversus totalis with cystic dysplasia of kidneys and pancreas", "situs inversus, cystic dysplastic kidney and pancreas, bowed lower limbs,severe intrauterine growth retardation, and oligohydramnios"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "situs inversus totalis with cystic dysplasia of kidneys and pancreas", "shortest_name_length": 68}
{"curie": "UMLS:C3839868", "names": ["CN-AML", "Normal karyotype acute myeloid leukemia", "Normal Karyotype Acute Myeloid Leukemia", "Acute myeloid leukemia with normal karyotype", "Cytogenetically Normal Acute Myeloid Leukemia", "Cytogenetically normal acute myeloid leukemia", "Cytogenetically normal acute myeloid leukaemia", "Acute myeloid leukemia with normal karyotype (disorder)", "Acute myeloid leukemia with normal karyotype (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cytogenetically normal acute myeloid leukemia", "shortest_name_length": 6}
{"curie": "UMLS:C1446220", "names": ["Basal ganglion stroke", "Basal ganglion infarct", "Basal ganglia infarction", "Infarction of basal ganglia", "cerebral infarction basal ganglia", "Infarction of basal ganglia (disorder)", "Infarction of basal ganglia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infarction of basal ganglia", "shortest_name_length": 21}
{"curie": "MONDO:0017352", "names": ["metabolic disorder; glutamine", "glutamine; metabolic disorder", "disorder of glutamine metabolism", "Disorder of glutamine metabolism", "Disturbance of glutamine metabolism", "Disorder of glutamine metabolism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of glutamine metabolism", "shortest_name_length": 29}
{"curie": "UMLS:C1515128", "names": ["T-Cell Large Granular Lymphocyte Leukemia, Common Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-Cell Large Granular Lymphocyte Leukemia, Common Variant", "shortest_name_length": 57}
{"curie": "MONDO:0003150", "names": ["Disease;genital;M", "Male Genital Disease", "genital disease male", "male genital disease", "Genital Disease, Male", "male genital diseases", "Genital disorder male", "Male Genital Diseases", "Disease, Male Genital", "male genital disorder", "diseases genital male", "male genital disorders", "Diseases, Male Genital", "Genital Diseases, Male", "Male Genital Disorders", "disorders genitals male", "male reproductive disease", "Genital disorder male NOS", "Male genital organ disease", "male reproductive disorder", "diseases genital male organ", "disorders male reproductive", "male reproductive disorders", "Male genital tract disorder", "REPRODUCTIVE DISORDERS, MALE", "genital organs; disorder, male", "Disorder of male genital organ", "DISEASES OF MALE GENITAL ORGANS", "Diseases of male genital organs", "disorder of male genital organs", "Male reproductive system disease", "male reproductive system disease", "Male Reproductive System Disease", "male reproductive system disorder", "Male Reproductive System Disorder", "Male reproductive system disorder", "Disease of male genital organs, NOS", "DISEASES OF THE MALE GENITAL ORGANS", "disease of male reproductive system", "disorder of male reproductive system", "Disorder of Male Reproductive System", "disorder of Male reproductive system", "Disorder of male reproductive system", "Disorder of male genital organ (disorder)", "disease (or disorder); genital organ, male", "Unspecified disorder of male genital organs", "disorder of male genital organs (diagnosis)", "male reproductive system disease or disorder", "Disorder of male genital organs, unspecified", "Disorder of male reproductive system (disorder)", "disease or disorder of male reproductive system", "DISEASES OF THE MALE GENITAL ORGANS: GENERAL TERMS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "male reproductive system disorder", "shortest_name_length": 17}
{"curie": "MONDO:0030487", "names": ["SMDP", "SPONDYLOMETAPHYSEAL DYSPLASIA, PAGNAMENTA TYPE", "spondylometaphyseal dysplasia, pagnamenta type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondylometaphyseal dysplasia, pagnamenta type", "shortest_name_length": 4}
{"curie": "MONDO:0012573", "names": ["VUR2", "Vesicoureteral Reflux 2", "vesicoureteral reflux 2", "VESICOURETERAL REFLUX 2", "vesicoureteral reflux type 2", "ROBO2 vesicoureteral reflux (disease)", "vesicoureteral reflux (disease) caused by mutation in ROBO2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vesicoureteral reflux 2", "shortest_name_length": 4}
{"curie": "MONDO:0008093", "names": ["Epidermal nevi", "Epidermal nevus", "nevus epidermal", "epidermal nevus", "Epidermal Nevus", "Nevus sebaceous", "Epidermal naevus", "Epithelial nevus", "Nevus, Epidermal", "Epidermal Naevus", "NEVUS, EPIDERMAL", "nevus, epidermal", "epidermal naevus", "Epithelial naevus", "Nevus, woolly hair", "Epidermal nevus, NOS", "Epidermal naevus, NOS", "Epithelial nevus, NOS", "Epithelial naevus, NOS", "epidermal nevus, somatic", "nevus, epidermal, somatic", "Epidermal nevus (disorder)", "epidermal nevus (diagnosis)", "nonepidermolytic keratinocytic nevus", "NEVUS, KERATINOCYTIC, NONEPIDERMOLYTIC", "Nevus, Keratinocytic, nonepidermolytic", "Nevus, Keratinocytic, Nonepidermolytic", "Epidermal nevus (morphologic abnormality)", "nevus sebaceous or woolly hair nevus, somatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nevus, epidermal", "shortest_name_length": 14}
{"curie": "MONDO:0013963", "names": ["DFNB93", "autosomal recessive deafness 93", "DEAFNESS, AUTOSOMAL RECESSIVE 93", "deafness, autosomal recessive 93", "deafness, autosomal recessive type 93", "autosomal recessive nonsyndromic deafness 93", "CABP2 autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 93", "autosomal recessive nonsyndromic deafness type 93", "autosomal recessive nonsyndromic deafness caused by mutation in CABP2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 93", "shortest_name_length": 6}
{"curie": "UMLS:C0001263", "names": ["actinomycosis abdominal", "Abdominal Actinomycosis", "Abdominal actinomycosis", "abdominal actinomycosis", "actinomycosis; abdominal", "Actinomycosis, abdominal", "abdominal; actinomycosis", "actinomycosis; gastrointestinal", "gastrointestinal; actinomycosis", "Abdominal actinomycotic infection", "Actinomycotic abdominal infection", "Abdominal actinomycosis (disorder)", "abdominal actinomycosis (diagnosis)", "Ray fungus disease of the intestines"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abdominal actinomycosis", "shortest_name_length": 23}
{"curie": "MONDO:0016949", "names": ["trisomy 16p", "16p trisomy", "16p+ syndrome", "Duplication 16p", "16p duplication", "dup(16p) syndrome", "partial trisomy 16p", "chromosome 16p trisomy", "16p duplication syndrome", "duplication 16p syndrome", "chromosome 16p duplication", "partial trisomy of chromosome 16p", "chromosome 16p duplication syndrome", "partial duplication of chromosome 16p", "partial trisomy of the short arm of chromosome 16", "partial duplication of the short arm of chromosome 16", "partial duplication of the short arm of chromosome type 16"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of the short arm of chromosome 16", "shortest_name_length": 11}
{"curie": "UMLS:C1370446", "names": ["Recurrent Multiple Myeloma", "Plasma cell myeloma relapse", "Relapsed Plasma Cell Myeloma", "Recurrent Plasma Cell Myeloma", "Plasma cell myeloma recurrent", "Recurrent Multiple Myeloma/Plasma Cell Myeloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Plasma cell myeloma recurrent", "shortest_name_length": 26}
{"curie": "MONDO:0003144", "names": ["MDEP", "Diktyoma", "Medulloepithelioma", "medulloepithelioma", "Diktyoma, malignant", "medulloepitheliomas", "Medulloepitheliomas", "Medulloepithelioma NOS", "Medulloepithelioma, NOS", "malignant medulloepithelioma", "Medulloepithelioma (disorder)", "malignant medulloepithelioma (diagnosis)", "central nervous system medulloepithelioma", "Central Nervous System Medulloepithelioma", "Medulloepithelioma Not Otherwise Specified", "Medulloepithelioma, Central Nervous System", "medulloepithelioma, central nervous system", "Medulloepithelioma, central nervous system", "Medulloepithelioma (morphologic abnormality)", "Medulloepithelioma of central nervous system", "Medulloepithelioma of the central nervous system", "medulloepithelioma NOS (morphologic abnormality)", "medulloepithelioma of the central nervous system", "Medulloepithelioma of central nervous system (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "medulloepithelioma", "shortest_name_length": 4}
{"curie": "UMLS:C0205734", "names": ["autoimmune diabetes", "Autoimmune Diabetes", "diabetes autoimmune", "Diabetes, Autoimmune"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diabetes, Autoimmune", "shortest_name_length": 19}
{"curie": "UMLS:C4683158", "names": ["Tumor Stage (Pathologic)", "Uveal Melanoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uveal Melanoma by AJCC v7 Stage", "shortest_name_length": 24}
{"curie": "MONDO:0011117", "names": ["Cysts of Iris Pigment Epithelium", "CYSTS OF IRIS PIGMENT EPITHELIUM", "cysts of iris pigment epithelium", "iris pigment epithelium anomalies", "Iris Pigment Epithelium Anomalies", "IRIS PIGMENT EPITHELIUM ANOMALIES", "Ruffles and Cysts of Iris Pigment Epithelium", "ruffles and cysts of iris pigment epithelium", "RUFFLES AND CYSTS OF IRIS PIGMENT EPITHELIUM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "iris pigment epithelium anomalies", "shortest_name_length": 32}
{"curie": "UMLS:C0013608", "names": ["edema; heart", "heart; edema", "Cardiac Edema", "Cardiac edema", "edema cardiac", "cardiac edema", "Cardiac Edemas", "Edema, Cardiac", "edema; cardiac", "cardiac; edema", "Cardiac oedema", "Edemas, Cardiac", "cardiac; hydrops", "hydrops; cardiac", "Cardiac induced edema", "edema; cardiovascular", "cardiovascular; edema", "Cardiac induced oedema", "Cardiac edema (disorder)", "Edema due to cardiac disease", "Oedema due to cardiac disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Edema, Cardiac", "shortest_name_length": 12}
{"curie": "UMLS:C5418768", "names": ["Recurrent Platinum-Resistant Fallopian Tube Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Platinum-Resistant Fallopian Tube Carcinoma", "shortest_name_length": 53}
{"curie": "UMLS:C0349489", "names": ["fetal hypoxia", "Fetal hypoxia", "Fetal Hypoxia", "fetus hypoxia", "Hypoxia, Fetal", "Foetal hypoxia", "Hypoxia in Utero", "In Utero Hypoxia", "Fetal hypoxia (disorder)", "fetal hypoxia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fetal Hypoxia", "shortest_name_length": 13}
{"curie": "MONDO:0018262", "names": ["FACS", "Fetal AEDS", "fetal AEDS", "fetal anticonvulsant syndrome", "Fetal anticonvulsant syndrome", "Foetal anticonvulsant syndrome", "fetal antiepileptic drug syndrome", "Fetal antiepileptic drug syndrome", "Fetus affected by placental transfer of anticonvulsant", "Foetus affected by placental transfer of anticonvulsant", "Fetus affected by placental transfer of anticonvulsant (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fetal anticonvulsant syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C2981714", "names": ["stage IA mycosis fungoides/Sezary syndrome", "Stage IA Mycosis Fungoides and Sézary Syndrome", "Stage IA Mycosis Fungoides and Sezary Syndrome", "Stage IA Mycosis Fungoides and Sezary Syndrome AJCC v7", "stage IA mycosis fungoides and Sezary syndrome AJCC v7", "Stage IA Mycosis Fungoides and Sézary Syndrome AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Mycosis Fungoides and Sezary Syndrome AJCC v7", "shortest_name_length": 42}
{"curie": "UMLS:C5419083", "names": ["Metastatic Ampulla of Vater Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Ampulla of Vater Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0012529", "names": ["DBA3", "Diamond-Blackfan Anemia 3", "DIAMOND-BLACKFAN ANEMIA 3", "Diamond-Blackfan anemia 3", "anemia Diamond-Blackfan 3", "Diamond-blackfan anemia 3", "Anemia, Diamond-Blackfan, 3", "RPS24 Diamond-Blackfan anemia", "Diamond-Blackfan Anemia type 3", "RPS24-related Diamond-Blackfan anemia", "Diamond-Blackfan anemia caused by mutation in RPS24"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diamond-Blackfan anemia 3", "shortest_name_length": 4}
{"curie": "MONDO:0008039", "names": ["ham", "HAM", "TSP", "ham/TSP", "HAM/TSP", "jamaican syndrome", "Jamaican syndrome", "jamaican neuropathy", "Jamaican neuropathy", "Tropical spastic paresis", "Tropical spastic paralysis", "HTLV-associated myelopathy", "tropical spastic paralysis", "Tropical Spastic Paraplegia", "tropical spastic paraplegia", "Tropical spastic paraplegia", "Tropical Spastic Parapareses", "Tropical Spastic Paraparesis", "HTLV-I-associated myelopathy", "tropical spastic paraparesis", "Htlv-1-Associated Myelopathy", "HTLV I Associated Myelopathy", "htlv i associated myelopathy", "HTLV 1-associated myelopathy", "Paraplegia, Tropical Spastic", "Tropical spastic paraparesis", "paraplegia; tropical spastic", "HTLV-I-Associated Myelopathy", "Spastic Paraplegia, Tropical", "Tropical Spastic Paraplegias", "spastic; paraplegia, tropical", "paraplegia; spastic, tropical", "Spastic Paraparesis, Tropical", "Paraplegias, Tropical Spastic", "Myelopathy, Htlv-1-Associated", "Spastic Parapareses, Tropical", "MYELOPATHY, HTLV-1-ASSOCIATED", "Parapareses, Tropical Spastic", "Paraparesis, Tropical Spastic", "myelopathy, HTLV-1-associated", "Myelopathy, HTLV-I-Associated", "Myelopathy, Htlv 1 Associated", "Spastic Paraplegias, Tropical", "tropical; paraplegia, spastic", "HTLV-I-Associated Myelopathies", "HTLV I Associated Myelopathies", "Htlv-1-Associated Myelopathies", "Myelopathies, Htlv-1-Associated", "Myelopathies, HTLV I Associated", "Myelopathies, HTLV-I-Associated", "tropical spastic paraparesis (TSP)", "TSP - Tropical spastic paraparesis", "HAM - HTLV 1-associated myelopathy", "Jamaican (tropical) myeloneuropathy", "tropical spastic paraparesis (formerly)", "tropical spastic paraplegia (diagnosis)", "Human T-cell leukemia virus type I myelopathy", "Human T-cell leukaemia virus type I myelopathy", "FAMILIAL SPASTIC PARAPARESIS, HTLV-1-ASSOCIATED", "Familial Spastic Paraparesis, Htlv-1-Associated", "Familial Spastic Paraparesis, Htlv 1 Associated", "familial spastic paraparesis, HTLV-1-associated", "Myelopathy caused by Human T-lymphotropic virus 1", "Human T-cell lymphotropic virus 1-associated myelopathy", "Human T-Lymphotropic Virus Type 1 Associated Myelopathy", "Human T Lymphotropic Virus Type 1 Associated Myelopathy", "Myelopathy, Human T-Lymphotropic Virus Type 1 Associated", "Myelopathy, Human T Lymphotropic Virus Type 1 Associated", "HTLV-1-associated myelopathy/tropical spastic paraparesis", "HTLV-I-Associated Myelopathy-Tropical Spastic Paraparesis", "HTLV-1 Associated Myelopathy/Tropical Spastic Paraparesis", "HTLV-1 associated myelopathy/tropical spastic paraparesis", "HTLV I Associated Myelopathy Tropical Spastic Paraparesis", "Myelopathy caused by Human T-lymphotropic virus 1 (disorder)", "Human T-lymphotropic virus type-1-associated myelopathy/tropical spastic paraparesis", "Human T-lymphotropic virus type I-associated myelopathy/tropical spastic paraparesis", "Human T-cell leukemia virus type 1 associated myelopathy/tropical spastic paraparesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tropical spastic paraparesis", "shortest_name_length": 3}
{"curie": "MONDO:0014786", "names": ["IGAN3", "SPRY2 IgA glomerulonephritis", "susceptibility to IgA nephropathy 3", "IgA NEPHROPATHY, SUSCEPTIBILITY TO, 3", "IgA nephropathy, susceptibility to, 3", "IgA nephropathy, susceptibility to, type 3", "IgA nephropathy, susceptibility to, 3; IGAN3", "IgA glomerulonephritis caused by mutation in SPRY2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IgA nephropathy, susceptibility to, 3", "shortest_name_length": 5}
{"curie": "UMLS:C5419074", "names": ["Recurrent Ocular Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Ocular Melanoma", "shortest_name_length": 25}
{"curie": "MONDO:0007936", "names": ["macular dystrophy, fenestrated sheen type", "Macular Dystrophy, Fenestrated Sheen Type", "MACULAR DYSTROPHY, FENESTRATED SHEEN TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macular dystrophy, fenestrated sheen type", "shortest_name_length": 41}
{"curie": "MONDO:0016750", "names": ["Halal syndrome", "Microcephaly cleft palate syndrome", "microcephaly-cleft palate syndrome", "Microcephalus cleft palate syndrome", "Microcephaly cleft palate autosomal dominant", "microcephaly cleft palate autosomal dominant", "Microcephalus cleft palate syndrome (disorder)", "microcephaly-cleft palate-abnormal retinal pigmentation syndrome", "Microcephaly-cleft palate-abnormal retinal pigmentation syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly-cleft palate syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0020653", "names": ["vagina adenocarcinoma", "Vagina Adenocarcinoma", "Vaginal adenocarcinoma", "Vaginal Adenocarcinoma", "vaginal adenocarcinoma", "adenocarcinoma of vagina", "Adenocarcinoma of Vagina", "Adenocarcinoma of the Vagina", "adenocarcinoma of the vagina", "vagina cancer, adenocarcinoma", "vaginal cancer, adenocarcinoma", "adenocarcinoma of vagina (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vaginal adenocarcinoma", "shortest_name_length": 21}
{"curie": "MONDO:0021547", "names": ["AI3B", "amelogenesis imperfecta type 3B", "amelogenesis imperfecta, type 3B", "AMELOGENESIS IMPERFECTA, TYPE IIIB", "amelogenesis imperfecta, type IIIB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amelogenesis imperfecta type 3B", "shortest_name_length": 4}
{"curie": "UMLS:C5421211", "names": ["Locally Advanced Lung Adenosquamous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Lung Adenosquamous Carcinoma", "shortest_name_length": 45}
{"curie": "UMLS:C1112364", "names": ["Human polyomavirus infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Human polyomavirus infection", "shortest_name_length": 28}
{"curie": "UMLS:C1335441", "names": ["Poorly Differentiated Angiosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Poorly Differentiated Angiosarcoma", "shortest_name_length": 34}
{"curie": "MONDO:0013624", "names": ["CDG2U", "RAFQS", "MRT15", "RAFIQ SYNDROME", "Rafiq syndrome", "MRT15, FORMERLY", "mental retardation, autosomal recessive 15", "intellectual disability, autosomal recessive 15", "mental retardation, autosomal recessive type 15", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15, FORMERLY", "MAN1B1 autosomal recessive non-syndromic intellectual disability", "autosomal recessive non-syndromic intellectual disability caused by mutation in MAN1B1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rafiq syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0003289", "names": ["Deep Leiomyoma", "deep leiomyoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deep leiomyoma", "shortest_name_length": 14}
{"curie": "MONDO:0007668", "names": ["GLOBULIN ANOMALY INVOLVING BETA (2A)-GLOBULIN", "globulin anomaly involving beta (2A)-globulin", "Globulin Anomaly involving Beta (2A)-Globulin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "globulin anomaly involving beta (2A)-globulin", "shortest_name_length": 45}
{"curie": "MONDO:0022981", "names": ["die Smulders droog van dijk syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "die Smulders droog van dijk syndrome", "shortest_name_length": 36}
{"curie": "MONDO:0009926", "names": ["EVMPS", "Escobar syndrome", "Escobar Syndrome", "pterygium syndrome", "pterygium universale", "pterygium Universale", "pterygium colli syndrome", "multiple pterygium syndrome", "multiple pterygium syndrome Escobar type", "multiple pterygium syndrome nonlethal type", "multiple pterygium syndrome, Nonlethal type", "Escobar variant multiple pterygium syndrome", "multiple pterygium syndrome, ESCOBAR variant", "autosomal recessive multiple pterygium syndrome", "multiple pterygium syndrome, autosomal recessive", "autosomal recessive non-lethal multiple pterygium syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive multiple pterygium syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C2347914", "names": ["Recurrent Spinal Cord Tumor", "recurrent childhood spinal cord tumor", "Recurrent Childhood Spinal Cord Tumor", "recurrent childhood spinal cord neoplasm", "Recurrent Childhood Spinal Cord Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Spinal Cord Neoplasm", "shortest_name_length": 27}
{"curie": "MONDO:0032657", "names": ["DEE69", "EIEE69", "early infantile epileptic encephalopathy 69", "developmental and epileptic encephalopathy 69", "epileptic encephalopathy, early infantile, 69", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 69", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 69", "developmental and epileptic encephalopathy, 69"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 69", "shortest_name_length": 5}
{"curie": "MONDO:0006421", "names": ["Small Intestinal Tubular Adenoma", "small intestinal tubular adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small intestinal tubular adenoma", "shortest_name_length": 32}
{"curie": "MONDO:0011062", "names": ["Aprosencephaly cerebellar dysgenesis", "aprosencephaly cerebellar dysgenesis", "Aprosencephaly and Cerebellar Dysgenesis", "APROSENCEPHALY AND CEREBELLAR DYSGENESIS", "aprosencephaly and cerebellar dysgenesis", "Aprosencephaly cerebellar dysgenesis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aprosencephaly cerebellar dysgenesis", "shortest_name_length": 36}
{"curie": "MONDO:0013427", "names": ["IMD31B", "STAT1 deficiency", "IMMUNODEFICIENCY 31B", "immunodeficiency 31B", "immunodeficiency type 31B", "autosomal recessive STAT1 deficiency", "STAT1 DEFICIENCY, AUTOSOMAL RECESSIVE", "Stat1 deficiency, autosomal recessive", "susceptibility to viral and mycobacterial infections", "predisposition to severe viral infection due to STAT1 deficiency", "susceptibility to viral and mycobacterial infections due to STAT1 deficiency", "autosomal recessive immunodeficiency 31B, mycobacterial and viral infections", "immunodeficiency 31B, mycobacterial and viral infections, autosomal recessive", "IMMUNODEFICIENCY 31B, MYCOBACTERIAL AND VIRAL INFECTIONS, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 31B", "shortest_name_length": 6}
{"curie": "MONDO:0000147", "names": ["polyposi", "Polyposis", "polyposis", "POLYPOSIS", "Polyposis, NOS", "Multiple Polyps", "multiple polyps", "Multiple polyps", "Multiple polyps (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyposis", "shortest_name_length": 8}
{"curie": "UMLS:C5419976", "names": ["Digestive System Kaposi Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Digestive System Kaposi Sarcoma", "shortest_name_length": 31}
{"curie": "MONDO:0045050", "names": ["NS", "Cataract nuclear", "nuclear cataract", "Nuclear cataract", "cataract nuclear", "Nuclear Cataract", "nuclear sclerosis", "Nuclear sclerosis", "sclerosis nuclear", "cataracts nuclear", "Cataract, nuclear", "lenticular sclerosis", "Nuclear cataract, NOS", "NS - Nuclear sclerosis", "Nuclear nonsenile cataract", "Nuclear Sclerotic Cataract", "nuclear sclerotic cataract", "Nuclear sclerotic cataract", "Cataract, nuclear sclerotic", "Nuclear cataract (disorder)", "Nuclear non-senile cataract", "nuclear cataract (diagnosis)", "Yellowish cloudy centre of lens", "Yellowish cloudy center of lens", "lens nucleus cataract (disease)", "cataract (disease) of lens nucleus", "nuclear cataract (physical finding)", "Nuclear sclerotic cataract (disorder)", "nuclear sclerotic cataract (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nuclear cataract", "shortest_name_length": 2}
{"curie": "MONDO:0018532", "names": ["adenocarcinoma of liver and IBT", "adenocarcinoma of the liver and IBT", "adenocarcinoma of liver and intrahepatic biliary tract", "adenocarcinoma of the liver and intrahepatic biliary tract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenocarcinoma of liver and intrahepatic biliary tract", "shortest_name_length": 31}
{"curie": "UMLS:C0280156", "names": ["Stage III", "stage III grade 1 follicular lymphoma", "Stage III Grade 1 Follicular Lymphoma", "Stage III Grade I Follicular Lymphoma", "Grade I Follicular Lymphoma Stage III", "Ann Arbor Stage III Grade 1 Follicular Lymphoma", "Stage III Follicular Small Cleaved Cell Lymphoma", "Follicular Small Cleaved Cell Lymphoma Stage III", "stage III follicular small cleaved cell lymphoma", "follicular small cleaved cell lymphoma, stage III", "stage III grade I follicular small cleaved cell lymphoma", "Grade I Follicular Small Cleaved Cell Lymphoma Stage III", "Stage III Grade I Follicular Small Cleaved Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage III Grade 1 Follicular Lymphoma", "shortest_name_length": 9}
{"curie": "MONDO:0023016", "names": ["duplication of leg mirror foot"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "duplication of leg mirror foot", "shortest_name_length": 30}
{"curie": "MONDO:0033371", "names": ["DEE62", "EIEE62", "early infantile epileptic encephalopathy 62", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 62", "epileptic encephalopathy, early infantile, 62", "developmental and epileptic encephalopathy 62", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 62", "developmental and epileptic encephalopathy, 62"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 62", "shortest_name_length": 5}
{"curie": "MONDO:0002090", "names": ["Eccrine tumor", "eccrine tumor", "Eccrine Tumor", "Eccrine Neoplasm", "eccrine neoplasm", "Eccrine Skin Tumor", "eccrine skin tumor", "eccrine skin neoplasm", "Eccrine Skin Neoplasm", "eccrine tumor of skin", "Eccrine Tumor of Skin", "eccrine neoplasm of skin", "Eccrine Neoplasm of Skin", "Eccrine Tumor of the Skin", "eccrine sweat gland tumor", "eccrine tumor of the skin", "eccrine neoplasm of the skin", "eccrine sweat gland neoplasm", "Eccrine Neoplasm of the Skin", "tumor of eccrine sweat gland", "neoplasm of eccrine sweat gland", "eccrine sweat gland neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eccrine sweat gland neoplasm", "shortest_name_length": 13}
{"curie": "MONDO:0014420", "names": ["ACLSD", "ALS Deficiency", "Acid-Labile Subunit Deficiency", "Acid-labile subunit deficiency", "acid-labile SUBUNIT deficiency", "ACID-LABILE SUBUNIT DEFICIENCY", "acid-labile subunit, deficiency of", "Decreased levels of acid labile subunit", "Short stature due to primary acid-labile subunit deficiency", "short stature due to primary acid-labile subunit deficiency", "Short stature due to primary acid labile subunit deficiency", "Short stature due to primary acid labile subunit deficiency (disorder)", "Reduced insulin like growth factor binding protein acid labile subunit level", "Reduced insulin like growth factor binding protein acid labile subunit concentration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short stature due to primary acid-labile subunit deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C0686328", "names": ["Carcinoma insitu;breast;M", "Male Breast Carcinoma In Situ", "Carcinoma in situ of male breast", "Carcinoma in situ of male breast, NOS", "carcinoma in situ of the breast (male)", "Carcinoma in situ of male breast (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carcinoma in situ of male breast", "shortest_name_length": 25}
{"curie": "MONDO:0016786", "names": ["PHM", "Partial mole", "partial Mole", "Partial Mole", "Partial Hydatid Mole", "partial hydatid Mole", "Partial Molar Pregnancy", "incomplete hydatid Mole", "Incomplete Hydatid Mole", "Partial molar pregnancy", "partial molar pregnancy", "Partial hydatidiform mole", "partial hydatidiform mole", "Partial Hydatidiform Mole", "incomplete molar pregnancy", "Partial Hydatidiform Moles", "Incomplete molar pregnancy", "Hydatidiform Mole, Partial", "hydatidiform mole; partial", "Incomplete Molar Pregnancy", "partial; hydatidiform mole", "Mole, Partial Hydatidiform", "mole; hydatidiform, partial", "Hydatidiform Moles, Partial", "Moles, Partial Hydatidiform", "Incomplete Hydatidiform Mole", "incomplete hydatidiform mole", "Incomplete hydatidiform mole", "mole; hydatidiform, incomplete", "PHM - Partial hydatidiform mole", "Incomplete hydatidiform mole (disorder)", "Incomplete and partial hydatidiform mole", "Partial hydatidiform mole (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial hydatidiform mole", "shortest_name_length": 3}
{"curie": "MONDO:0019123", "names": ["CSWS", "CSWSS syndrome", "continuous spikes and waves during sleep", "Continuous spike and waves during slow sleep", "continuous spikes and waves during slow-wave sleep", "Electrical status epilepticus during slow-wave sleep", "epileptic encephalopathy with continuous spike-and-wave during slow sleep"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "continuous spikes and waves during sleep", "shortest_name_length": 4}
{"curie": "MONDO:0014180", "names": ["EBS3", "EBSB2", "EBS-AR BP230", "DST-related epidermolysis bullosa simplex", "epidermolysis bullosa simplex, autosomal recessive 2", "epidermolysis bullosa simplex due to BP230 deficiency", "epidermolysis bullosa simplex, autosomal recessive type 2", "EPIDERMOLYSIS BULLOSA SIMPLEX 3, LOCALIZED OR GENERALIZED INTERMEDIATE, WITH BP230", "EPIDERMOLYSIS BULLOSA SIMPLEX 3, LOCALIZED OR GENERALIZED INTERMEDIATE, WITH BP230 DEFICIENCY", "epidermolysis bullosa simplex 3, localized or generalized intermediate, with bp230 deficiency", "epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0000524", "names": ["mixed extragonadal germ cell cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed extragonadal germ cell cancer", "shortest_name_length": 35}
{"curie": "UMLS:C1333272", "names": ["Demyelinating Encephalopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Demyelinating Encephalopathy", "shortest_name_length": 28}
{"curie": "MONDO:0013167", "names": ["PARK16", "Parkinson disease 16", "parkinson disease 16", "PARKINSON DISEASE 16", "Parkinson Disease 16"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parkinson disease 16", "shortest_name_length": 6}
{"curie": "MONDO:0044885", "names": ["Tonsil Lipoma", "tonsil lipoma", "lipoma of tonsil", "Tonsillar Lipoma", "tonsillar lipoma", "Lipoma of Tonsil", "Lipoma of the Tonsil", "lipoma of the tonsil"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tonsillar lipoma", "shortest_name_length": 13}
{"curie": "UMLS:C5447540", "names": ["Myxoid Pleomorphic Liposarcoma", "Pleomorphic Myxoid Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myxoid Pleomorphic Liposarcoma", "shortest_name_length": 30}
{"curie": "UMLS:C0152159", "names": ["Uterine hypotonus", "Latent Phase Arrest", "Primary uterine inertia", "primary uterine inertia", "Uterine inertia, primary", "uterus; inertia, primary", "hypotonic uterine inertia", "Hypotonic uterine inertia", "Primary dysfunctional labor", "Primary dysfunctional labour", "hypotonic uterine dysfunction", "Hypotonic uterine dysfunction", "Prolonged Latent Phase of Labor", "prolonged latent phase of labor", "Primary inadequate contractions", "Prolonged latent phase of labor", "Prolonged latent phase of labour", "Hypotonic uterine dysfunction NOS", "Primary hypotonic uterine inertia", "Primary uterine inertia (disorder)", "primary uterine inertia (diagnosis)", "Arrest of Labor in the Latent Phase", "Hypotonic uterine inertia (disorder)", "primary hypotonic uterine dysfunction", "hypotonic uterine inertia (diagnosis)", "Primary hypotonic uterine dysfunction", "inertia; uterus, during labor, primary", "Hypotonic uterine dysfunction, primary", "Prolonged latent phase of labor (disorder)", "prolonged latent phase of labor (diagnosis)", "Primary hypotonic uterine dysfunction (disorder)", "primary hypotonic uterine dysfunction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypotonic uterine inertia", "shortest_name_length": 17}
{"curie": "UMLS:C0475734", "names": ["Perinatal intracranial hemorrhage", "Perinatal Intracranial Hemorrhage", "Perinatal intracranial haemorrhage", "Perinatal intracranial hemorrhage (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perinatal intracranial hemorrhage", "shortest_name_length": 33}
{"curie": "MONDO:0022755", "names": ["Mosaic monosomy 18", "monosomy 18 mosaicism", "Monosomy 18 mosaicism", "Mosaic monosomy chromosome 18", "chromosome 18 mosaic monosomy", "Chromosome 18 mosaic monosomy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 18 mosaic monosomy", "shortest_name_length": 18}
{"curie": "MONDO:0023059", "names": ["Elliott ludman Teebi syndrome", "Elliott Ludman Teebi syndrome", "multiple congenital anomalies, severe psychomotor retardation and symmetrical circumferential skin creases of arms and legs"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Elliott ludman Teebi syndrome", "shortest_name_length": 29}
{"curie": "MONDO:0001728", "names": ["active vestibular Meniere disease", "Vestibular active Mnire's disease", "Active vestibular Ménière disease", "vestibular active Mnire's disease", "Active vestibular Meniere's disease", "active vestibular Meniere's disease", "Vestibular active Meniere's disease", "Active vestibular Ménière's disease", "active Meniere's disease, vestibular", "Active Ménière's disease, vestibular", "Active Meniere's disease, vestibular", "Active vestibular Ménière's disease (disorder)", "active vestibular Meniere's disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "active vestibular Meniere disease", "shortest_name_length": 33}
{"curie": "MONDO:0007650", "names": ["MALT", "maltoma", "Maltoma", "MALToma", "BALToma", "maltomas", "Immunocytoma", "BALT lymphoma", "MALT Lymphoma", "MALT LYMPHOMA", "MALT lymphoma", "malt lymphoma", "BALT Lymphoma", "MALT-lymphoma", "MALT Lymphomas", "Lymphoma, MALT", "Lymphomas, MALT", "Lung MALT Lymphoma", "marginal zone lymphoma", "Marginal zone lymphoma", "Bronchial MALT Lymphoma", "Pulmonary MALT Lymphoma", "lymphoma, MALT, somatic", "Primary gastric lymphoma", "gastric lymphoma, primary", "MALT lymphoma of the dura", "Gastric Lymphoma, Primary", "GASTRIC LYMPHOMA, PRIMARY", "Mucosa-associated lymphoma", "nodal marginal zone lymphoma", "Nodal marginal zone lymphoma", "marginal zone b cell lymphoma", "Marginal Zone B Cell Lymphoma", "marginal zone b-cell lymphoma", "Marginal Zone B-Cell Lymphoma", "Lymphoma, B-Cell, Marginal Zone", "Familial primary gastric lymphoma", "familial primary gastric lymphoma", "lymphoid tissue, mucosa-associated", "Mucosa-associated lymphoma (disorder)", "Mucosa-associated lymphoma (diagnosis)", "Extranodal marginal zone B-cell lymphoma", "LYMPHOMA, MUCOSA-ASSOCIATED LYMPHOID TYPE", "lymphoma, mucosa-associated lymphoid type", "Mucosa-associated lymphoid tissue lymphoma", "mucosa-associated lymphoid tissue lymphoma", "Mucosa-Associated Lymphoid Tissue Lymphoma", "Mucosa Associated Lymphoid Tissue Lymphoma", "Mucosa-associated lymphatic tissue lymphoma", "mucosa-associated lymphatic tissue lymphoma", "Lymphoma, Mucosa-Associated Lymphoid Tissue", "Lymphoma, Mucosa Associated Lymphoid Tissue", "Mucosal-associated lymphoid tissue lymphoma", "Bronchus-associated lymphoid tissue lymphoma", "Bronchus-Associated Lymphoid Tissue Lymphoma", "Bronchial-associated lymphoid tissue lymphoma", "lymphoma of mucosa-associated lymphoid tissue", "Lymphoma of Mucosa Associated Lymphoid Tissue", "Lymphoma of Mucosa-Associated Lymphoid Tissue", "Lung Mucosa-Associated Lymphoid Tissue Lymphoma", "mucosa associated lymphoid tissue (MALT) lymphoma", "Pulmonary Mucosa-Associated Lymphoid Tissue Lymphoma", "Bronchial Mucosa-Associated Lymphoid Tissue Lymphoma", "marginal zone B-cell lymphoma of reticuloendothelial system", "extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue", "Extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue", "Extranodal Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue", "marginal zone B-cell lymphoma of reticuloendothelial system (diagnosis)", "Lung Extranodal Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue", "extranodal marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue", "Extranodal Marginal Zone B-Cell Lymphoma of Mucosa-Associated Lymphoid Tissue", "Extranodal marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue", "extranodal marginal zone B-cell lymphoma of mucosa associated lymphoid tissue", "Pulmonary Extranodal Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue", "extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue (MALT lymphoma)", "Extranodal marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue (disorder)", "extranodal marginal zone B-cell lymphoma of mucosa associated lymphoid tissue (diagnosis)", "Extranodal marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue (MALT-lymphoma)", "Extranodal marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue [MALT-lymphoma]", "Extranodal marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MALT lymphoma", "shortest_name_length": 4}
{"curie": "UMLS:C2242642", "names": ["Engraft failure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Engraft failure", "shortest_name_length": 15}
{"curie": "UMLS:C1336347", "names": ["Stage IVA Salivary Gland Cancer", "Stage IVA Major Salivary Gland Cancer", "Stage IVA Major Salivary Gland Carcinoma", "Stage IVA Major Salivary Gland Cancer AJCC v7", "Stage IVA Major Salivary Gland Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Major Salivary Gland Cancer AJCC v7", "shortest_name_length": 31}
{"curie": "MONDO:0018974", "names": ["Paraneoplastic pemphigus", "paraneoplastic pemphigus", "pemphigus paraneoplastic", "paraneoplastic pemphigus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paraneoplastic pemphigus", "shortest_name_length": 24}
{"curie": "MONDO:0008355", "names": ["IHPS1", "Infantile Pyloric Stenoses", "Infantile Pyloric Stenosis", "pyloric stenosis, infantile", "Stenosis, Infantile Pyloric", "Pyloric Stenosis, Infantile", "Infantile Hypertrophic Pyloric Stenosis", "pyloric stenosis, infantile hypertrophic", "Pyloric Stenosis, Infantile Hypertrophic", "Pyloric Stenosis, Infantile Hypertrophic 1", "PYLORIC STENOSIS, INFANTILE HYPERTROPHIC, 1", "pyloric stenosis, infantile hypertrophic, 1", "IHPS1 Infantile Hypertrophic Pyloric Stenosis 1", "pyloric stenosis, infantile hypertrophic 1, multifactorial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyloric stenosis, infantile hypertrophic, 1", "shortest_name_length": 5}
{"curie": "MONDO:0015369", "names": ["JSRD", "Joubert syndrome and related disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome and related disorders", "shortest_name_length": 4}
{"curie": "UMLS:C4553666", "names": ["Stage IIIB Fallopian Tube Cancer", "Stage IIIB Fallopian Tube Cancer AJCC v8", "Stage IIIB Fallopian Tube Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Fallopian Tube Cancer AJCC v8", "shortest_name_length": 32}
{"curie": "UMLS:C1881254", "names": ["Inverted papilloma", "Inverted Squamous Cell Papilloma", "Squamous cell papilloma, inverted", "Inverted papilloma, squamous cell", "Squamous cell papilloma, inverted (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Inverted Squamous Cell Papilloma", "shortest_name_length": 18}
{"curie": "EFO:0005039", "names": ["hippocampal atrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hippocampal atrophy", "shortest_name_length": 19}
{"curie": "UMLS:C1519663", "names": ["Ovarian Sertoli Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Sertoli Cell Tumor", "shortest_name_length": 26}
{"curie": "MONDO:0004392", "names": ["intracranial chondrosarcoma", "Brain Extraskeletal Myxoid Chondrosarcoma", "Intracranial Extraskeletal Myxoid Chondrosarcoma", "intracranial extraskeletal myxoid chondrosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intracranial extraskeletal myxoid chondrosarcoma", "shortest_name_length": 27}
{"curie": "UMLS:C3897968", "names": ["Penetrating Open Globe Injury", "Penetrating open globe injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Penetrating open globe injury", "shortest_name_length": 29}
{"curie": "MONDO:0014198", "names": ["MTDPS13", "FBXL4 deficiency", "mitochondrial DNA depletion syndrome 13", "Mitochondrial DNA Depletion Syndrome 13", "FBXL4 mitochondrial DNA depletion syndrome", "mitochondrial DNA depletion syndrome type 13", "BXL4-related early-onset mitochondrial encephalopathy", "FBXL4-related early onset mitochondrial encephalopathy", "encephalomyopathic mitochondrial DNA depletion syndrome-13", "Mitochondrial DNA depletion syndrome 13 encephalomyopathic type", "mitochondrial DNA depletion syndrome caused by mutation in FBXL4", "mitochondrial DNA depletion syndrome 13, encephalomyopathic type", "MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)", "mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)", "FBXL4-related encephalomyopathic mitochondrial DNA depletion syndrome", "mtDNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies", "FBXL4 (F-box and leucine rich repeat protein 4) related early onset mitochondrial encephalopathy", "mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies", "F-box and leucine rich repeat protein 4 related mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form", "F-box and leucine rich repeat protein 4 related mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial DNA depletion syndrome 13", "shortest_name_length": 7}
{"curie": "MONDO:0016378", "names": ["hyperthermia induced defects", "Hyperthermia-induced defect, NOS", "Birth defect due to maternal hyperthermia", "Maternal hyperthermia induced birth defect", "Maternal hyperthermia-induced birth defects", "maternal hyperthermia induced birth defects", "Birth defect due to maternal hyperthermia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maternal hyperthermia induced birth defects", "shortest_name_length": 28}
{"curie": "MONDO:0700129", "names": ["mosaic translocation Down syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mosaic translocation Down syndrome", "shortest_name_length": 34}
{"curie": "MONDO:0019450", "names": ["LCH", "lissencephaly with cerebellar hypoplasia", "Lissencephaly with cerebellar hypoplasia", "Lissencephaly co-occurrent with congenital cerebellar hypoplasia", "Lissencephaly co-occurrent with congenital cerebellar hypoplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lissencephaly with cerebellar hypoplasia", "shortest_name_length": 3}
{"curie": "MONDO:0054733", "names": ["SPGF29", "spermatogenic failure 29", "SPERMATOGENIC FAILURE 29"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 29", "shortest_name_length": 6}
{"curie": "UMLS:C0334061", "names": ["Dyskeratosis", "dyskeratosis", "Dyskeratosis, NOS", "Dyskeratosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dyskeratosis", "shortest_name_length": 12}
{"curie": "MONDO:0012614", "names": ["MRT6", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 6", "Mental Retardation, Autosomal Recessive 6", "mental retardation, autosomal recessive 6", "mental retardation, autosomal recessive type 6", "intellectual disability, autosomal recessive 6", "intellectual disability, autosomal recessive type 6", "autosomal recessive intellectual developmental disorder 6", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 6", "intellectual developmental disorder, autosomal recessive 6", "GRIK2 autosomal recessive non-syndromic intellectual disability", "autosomal recessive non-syndromic intellectual disability caused by mutation in GRIK2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 6", "shortest_name_length": 4}
{"curie": "MONDO:0014186", "names": ["RP82", "ARL2BP retinitis pigmentosa", "retinitis pigmentosa caused by mutation in ARL2BP", "retinitis pigmentosa with or without situs inversus", "RETINITIS PIGMENTOSA 82 WITH OR WITHOUT SITUS INVERSUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa with or without situs inversus", "shortest_name_length": 4}
{"curie": "UMLS:C4726553", "names": ["Myeloid Neoplasms with Germline GATA2 Mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myeloid Neoplasms with Germline GATA2 Mutation", "shortest_name_length": 46}
{"curie": "MONDO:0008275", "names": ["FEO", "EOF", "HEPOD", "MCCABE DISEASE", "Mccabe disease", "McCabe disease", "familial expansile osteolysis", "Familial expansile osteolysis", "FAMILIAL EXPANSILE OSTEOLYSIS", "osteolysis, familial expansile", "Osteolysis, familial expansile", "EXPANSILE OSTEOLYSIS, FAMILIAL", "Expansile osteolysis, familial", "expansile osteolysis, familial", "Familial expansile osteolysis (disorder)", "osteolysis idiopathic familial expansile", "Familial expansile osteolysis (diagnosis)", "hereditary expansile polyostotic osteolytic dysplasia", "Hereditary expansile polyostotic osteolytic dysplasia", "Polyostotic osteolytic dysplasia, hereditary expansile", "polyostotic osteolytic dysplasia, hereditary expansile", "POLYOSTOTIC OSTEOLYTIC DYSPLASIA, HEREDITARY EXPANSILE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial expansile osteolysis", "shortest_name_length": 3}
{"curie": "MONDO:0013493", "names": ["ACACAD", "ACC deficiency", "ACC1 DEFICIENCY", "Acc1 deficiency", "Acaca deficiency", "ACACA Deficiency", "ACACA DEFICIENCY", "ACETYL-CoA carboxylase deficiency", "Acetyl-Coa Carboxylase Deficiency", "ACETYL-CoA CARBOXYLASE DEFICIENCY", "acetyl-coa carboxylase deficiency", "Acetyl-CoA carboxylase deficiency", "Acetyl-CoA: carboxylase deficiency", "Deficiency of acetyl-CoA carboxylase", "Deficiency of acetyl-coenzyme A carboxylase", "Deficiency of acetyl-coenzyme A carboxylase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acetyl-coa carboxylase deficiency", "shortest_name_length": 6}
{"curie": "MONDO:0011024", "names": ["DH", "Duhring's disease", "Brocq-Duhring disease", "Duhring Brocq disease", "Dermatitis herpetiformis, familial", "DERMATITIS HERPETIFORMIS, FAMILIAL", "dermatitis herpetiformis, familial", "hereditary dermatitis herpetiformis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermatitis herpetiformis, familial", "shortest_name_length": 2}
{"curie": "MONDO:0007345", "names": ["coarctation", "Coarctation", "Aorta Coarctation", "coarctation aorta", "Aorta coarctation", "aorta coarctation", "Coarctation;aorta", "AORTA COARCTATION", "AORTIC COARCTATION", "Aorta Coarctations", "Aortic coarctation", "aortic coarctation", "AORTA, COARCTATION", "coarctation aortic", "Narrowing of aorta", "Aortic Coarctation", "Coarctation, Aortic", "Aortic Coarctations", "Coarctation of aorta", "coarctation of aorta", "Coarctation of Aorta", "Coarctations, Aortic", "COARCTATION OF AORTA", "aorta coarctation of", "Narrowing of the aorta", "COARCTATION OF THE AORTA", "coarctation of the aorta", "Coarctation of the aorta", "Coarctation of the Aorta", "Coarctation of aorta (disorder)", "coarctation of aorta (diagnosis)", "Coarctation of aorta (preductal) (postductal)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aorta coarctation", "shortest_name_length": 11}
{"curie": "MONDO:0008365", "names": ["Rec8 syndrome", "REC8 SYNDROME", "8 rec syndrome", "Rec(8) syndrome", "Rec(8) Syndrome", "rec(8) syndrome", "Recombinant 8 Syndrome", "8 recombinant syndrome", "recombinant 8 syndrome", "Recombinant 8 syndrome", "SAN LUIS VALLEY SYNDROME", "San Luis Valley syndrome", "Duplication 8q/deletion 8p", "Recombinant chromosome 8 syndrome", "chromosome 8 recombinant syndrome", "RECOMBINANT chromosome 8 syndrome", "RECOMBINANT CHROMOSOME 8 SYNDROME", "recombinant chromosome 8 syndrome", "Recombinant chromosome 8 syndrome (disorder)", "San Luis Valley recombinant chromosome 8 syndrome", "CHROMOSOME 8q22.1-qter DUPLICATION AND 8pter-p23.1 DELETION", "chromosome 8Q22.1-qter Duplication and 8Pter-p23.1 deletion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "recombinant 8 syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0044346", "names": ["echinococcus granulosus", "Echinococcus; granulosus", "granulosus; Echinococcus", "Unilocular hydatid disease", "unilocular hydatid disease", "Echinococcus granulosus infection", "echinococcus granulosus infection", "echinococcus granulosus (diagnosis)", "echinococcus granulosus infectious disease", "Echinococcus granulosus infectious disease", "Echinococcus granulosus disease or disorder", "Echinococcus granulosus infection (disorder)", "Tapeworm infection by Echinococcus granulosus", "Echinococcus granulosus infection, unspecified", "Echinococcus granulosus caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "echinococcus granulosus infectious disease", "shortest_name_length": 23}
{"curie": "MONDO:0003466", "names": ["Spindle Cell Synovial Sarcoma", "synovial spindle cell sarcoma", "spindle cell synovial sarcoma", "Synovial sarcoma, spindle cell", "Synovial sarcoma - spindle cell", "Synovial sarcoma, spindle cell type", "synovial sarcoma, monophasic fibrous", "Synovial sarcoma, monophasic fibrous", "spindle cell synovial sarcoma (diagnosis)", "Synovial Sarcoma with Spindle Cell Components", "Synovial sarcoma with spindle cell Components", "synovial sarcoma with spindle cell components", "Synovial sarcoma, spindle cell (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spindle cell synovial sarcoma", "shortest_name_length": 29}
{"curie": "UMLS:C5236042", "names": ["Abdominal Neoplasm, Excluding Pancreas Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abdominal Neoplasm, Excluding Pancreas Neoplasm", "shortest_name_length": 47}
{"curie": "MONDO:0012861", "names": ["Pof6", "POF6", "Premature Ovarian Failure 6", "PREMATURE OVARIAN FAILURE 6", "premature ovarian failure 6", "FIGLA primary ovarian failure", "primary ovarian insufficiency 6", "premature ovarian failure type 6", "primary ovarian failure caused by mutation in FIGLA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "premature ovarian failure 6", "shortest_name_length": 4}
{"curie": "UMLS:C4727087", "names": ["Metastatic Lung Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Lung Carcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0002132", "names": ["skull cancer", "cancer of skull", "malignant skull neoplasm", "malignant neoplasm of skull"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skull cancer", "shortest_name_length": 12}
{"curie": "MONDO:0006077", "names": ["adrenal medulla hyperplasia", "Adrenal Medullary Hyperplasia", "adrenal medullary hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adrenal medullary hyperplasia", "shortest_name_length": 27}
{"curie": "UMLS:C1868703", "names": ["Tracheitis", "Bacterial Tracheitis", "Bacterial tracheitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bacterial tracheitis", "shortest_name_length": 10}
{"curie": "UMLS:C1335433", "names": ["Pleural Carcinomatosis", "Carcinomatosis of the Pleura"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pleural Carcinomatosis", "shortest_name_length": 22}
{"curie": "MONDO:0014159", "names": ["SCAR14", "SPARCA", "SPARCA1", "SPTBN2 autosomal recessive cerebellar ataxia", "autosomal recessive spinocerebellar ataxia 14", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 14", "spinocerebellar ataxia, autosomal recessive 14", "Autosomal recessive spinocerebellar ataxia type 14", "autosomal recessive spinocerebellar ataxia type 14", "spinocerebellar ataxia, autosomal recessive type 14", "Spectrin-associated autosomal recessive cerebellar ataxia", "spectrin-associated autosomal recessive cerebellar ataxia", "cerebellar ataxia, autosomal recessive, spectrin-associated, 1", "CEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE, SPECTRIN-ASSOCIATED, 1", "autosomal recessive cerebellar ataxia-cognitive defect syndrome", "Spectrin-associated autosomal recessive cerebellar ataxia type 1", "spectrin-associated autosomal recessive cerebellar ataxia type 1", "Autosomal recessive cerebellar ataxia, cognitive defect syndrome", "Infantile-onset spinocerebellar ataxia-psychomotor delay syndrome", "infantile-onset spinocerebellar ataxia-psychomotor delay syndrome", "autosomal recessive cerebellar ataxia caused by mutation in SPTBN2", "Ataxie spinocérébelleuse à début infantile avec retard psychomoteur", "Spectrin-associated autosomal recessive cerebellar ataxia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive spinocerebellar ataxia 14", "shortest_name_length": 6}
{"curie": "MONDO:0008094", "names": ["CMC", "Stork bite", "stork bite", "bites stork", "Unna's nevus", "Unna's naevus", "Nevus simplex", "nevus flammeus", "Flammeus Nevus", "Portwine Nevus", "Nevus flammeus", "Portwine nevus", "portwine stain", "flammeus nevus", "Portwine stain", "Naevus simplex", "Nevus Flammeus", "portwine stains", "port wine Nevus", "Port wine stain", "naevus flammeus", "Port Wine Nevus", "port wine; spot", "Port Wine Stain", "spot; port wine", "nevus; portwine", "port-wine stain", "Naevus flammeus", "port wine nevus", "Port-wine stain", "port stain wine", "stain, portwine", "flammeus; nevus", "Port-Wine Stain", "nevus; flammeus", "port wine stain", "Port-wine nevus", "PORT-WINE STAIN", "Portwine naevus", "Port wine nevus", "PORT WINE STAIN", "Port-Wine Stains", "port stains wine", "Stain, Port-Wine", "Port wine naevus", "Port-wine naevus", "Stains, Port-Wine", "Salmon patch nevus", "Salmon patch Nevus", "Salmon Patch Nevus", "port-wine birthmark", "Port Wine Birthmark", "Salmon patch naevus", "port wine birthmark", "Hemangioma flammeus", "Port-wine birthmark", "PWS - Port-wine stain", "Port wine stain of skin", "Port-wine stain of skin", "port-wine stain of skin", "capillary malformations", "Port-Wine Stain of Skin", "Port Wine Stain of Skin", "port wine stain of skin", "port wine type hemangioma", "congenital nevus flammeus", "Port Wine Type Hemangioma", "nevus flammeus (diagnosis)", "port wine nevus (diagnosis)", "Port Wine Stain of the Skin", "port wine stain of the skin", "Port-wine stain of skin, NOS", "Salmon patch nevus (disorder)", "Familial multiple nevi flammei", "familial multiple nevi flammei", "NEVI FLAMMEI, FAMILIAL MULTIPLE", "Familial multiple naevi flammei", "Nevi flammei, familial multiple", "nevi flammei, familial multiple", "nevus flammeus (port wine nevus)", "port-wine stain familial multiple", "Port-wine stain familial multiple", "congenital capillary malformations", "Familial multiple port-wine stains", "Port-wine stain of skin (disorder)", "familial multiple port-wine stains", "capillary malformations, congenital", "Familial multiple nevi flammei (disorder)", "nevus flammeus (port wine nevus) (physical finding)", "capillary malformations, congenital, 1, somatic, mosaic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial multiple nevi flammei", "shortest_name_length": 3}
{"curie": "UMLS:C0000786", "names": ["Miscarriage", "miscarriage", "Miscarriage, NOS", "Spontaneous abortion", "Spontaneous Abortion", "ABORTION SPONTANEOUS", "Abortion;spontaneous", "abortion spontaneous", "SPONTANEOUS ABORTION", "Abortion spontaneous", "spontaneous abortion", "spontaneous; abortion", "Abortion, spontaneous", "spontaneous abortions", "Spontaneous Abortions", "ABORTION, SPONTANEOUS", "Abortions spontaneous", "abortions spontaneous", "abortion; spontaneous", "Abortion, Spontaneous", "Abortions.spontaneous", "Abortions, Spontaneous", "Abortion (Spontaneous)", "Abortion spontaneous NOS", "Spontaneous abortion NOS", "Spontaneous abortion, NOS", "Vaginal expulsion of fetus", "Spontaneous abortion, fetus", "abortion; spontaneous, fetus", "spontaneous; abortion, fetus", "spontaneous abortion (diagnosis)", "Vaginal expulsion of product of conception"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spontaneous abortion", "shortest_name_length": 11}
{"curie": "UMLS:C0855008", "names": ["PNET of bone metastatic", "Metastatic Peripheral Neuroepithelioma of Bone", "Peripheral neuroepithelioma of bone metastatic", "Metastatic Peripheral Primitive Neuroectodermal Tumor of Bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peripheral neuroepithelioma of bone metastatic", "shortest_name_length": 23}
{"curie": "MONDO:0029143", "names": ["IDDHDF", "chromosome 14q32 deletion syndrome", "CHROMOSOME 14q32 DELETION SYNDROME", "INTELLECTUAL DEVELOPMENTAL disorder WITH HYPERTELORISM AND DISTINCTIVE FACIES", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPERTELORISM AND DISTINCTIVE FACIES", "intellectual developmental disorder with hypertelorism and distinctive facies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder with hypertelorism and distinctive facies", "shortest_name_length": 6}
{"curie": "MONDO:0019288", "names": ["Dyschromia", "skin pigment", "pigment skin", "pigments skin", "Skin pigmented", "pigmented skin", "Other dyschromia", "Pigmen Disorders", "pigment disorder", "pigment disorders", "Pigment alteration", "Pigment Alterations", "pigmentation disease", "pigmentation disorder", "Pigmentation Disorder", "Pigmentation disorder", "pigmentation; disorder", "Disorder, Pigmentation", "disorders pigmentation", "pigmentation disorders", "Pigmentation Disorders", "disorder; pigmentation", "Pigmentation disorders", "Pigment alteration, NOS", "Disorders, Pigmentation", "Disorder of pigmentation", "Pigmentation disorder NOS", "skin pigmentation disorder", "Skin Pigmentation Disorder", "Skin pigmentation disorder", "disorder pigmentation skin", "Skin Pigmentation Disorders", "skin pigmentation disorders", "SKIN PIGMENTATION DISORDERS", "disorders pigmentation skin", "Disorder of skin pigmentation", "Skin pigmentation disorder, NOS", "pigmentation anomaly of the skin", "zone of skin pigmentation disease", "pigmentation disorder (diagnosis)", "Disorder of pigmentation (disorder)", "Anomalous pigmentation of skin, NOS", "pigmentation disease of zone of skin", "Disorder of pigmentation, unspecified", "Disorder of skin pigmentation (disorder)", "Pigment alteration (morphologic abnormality)", "Miscellaneous disorders of skin pigmentation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin pigmentation disorder", "shortest_name_length": 10}
{"curie": "UMLS:C3272619", "names": ["Chronic Acalculous Cholecystitis", "Chronic acalculous cholecystitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic acalculous cholecystitis", "shortest_name_length": 32}
{"curie": "MONDO:0008124", "names": ["paraomphalocele", "OMPHALOCELE, AUTOSOMAL", "omphalocele, autosomal", "chromosome 1P31 Duplication syndrome", "CHROMOSOME 1p31 DUPLICATION SYNDROME", "type - hypogastric - defect in the caudal fold", "type - epigastric - defect in the cephalic fold", "omphalocele due to duplication of 1p31.3, isolated cases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "omphalocele, autosomal", "shortest_name_length": 15}
{"curie": "MONDO:0022832", "names": ["congenital heart disease radio ulnar synostosis intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital heart disease radio ulnar synostosis intellectual disability", "shortest_name_length": 71}
{"curie": "MONDO:0020765", "names": ["CHN2", "neuropathy, congenital hypomyelinating, 2", "hypomyelinating neuropathy, congenital, 2", "NEUROPATHY, CONGENITAL HYPOMYELINATING, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuropathy, congenital hypomyelinating, 2", "shortest_name_length": 4}
{"curie": "MONDO:0007416", "names": ["AAN", "BEN", "DEFN", "Balkan; nephritis", "nephritis; Balkan", "Balkan Nephropathy", "Balkan nephropathy", "Nephropathy, Balkan", "Balkan; nephropathy", "endemic nephropathy", "Endemic Nephropathy", "nephropathy; Balkan", "NEPHROPATHIA EPIDEMICA", "nephropathia epidemica", "Balkan nephritis syndrome", "Balkan Endemic Nephropathy", "Balkan endemic nephropathy", "BALKAN ENDEMIC NEPHROPATHY", "Nephropathy, Balkan Endemic", "Endemic Nephropathy, Balkan", "Balkan nephropathy (disorder)", "aristolochic acid nephropathy", "Aristolochic acid nephropathy", "Aristolochic Acid Nephropathy", "Balkan nephropathy (diagnosis)", "Chinese herb endemic nephropathy", "Chinese Herb Endemic Nephropathy", "DANUBIAN ENDEMIC FAMILIAL NEPHROPATHY", "Danubian endemic familial nephropathy", "Danubian Endemic Familial Nephropathy", "Aristolochic acid nephropathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Balkan nephropathy", "shortest_name_length": 3}
{"curie": "UMLS:C4054043", "names": ["Secondary Peripheral Chondrosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary Peripheral Chondrosarcoma", "shortest_name_length": 35}
{"curie": "MONDO:0005246", "names": ["osteomyelitis", "OSTEOMYELITIS", "Osteomyelitis", "bone infection", "Bone Infection", "BONE INFECTION", "Bone infection", "infection; bone", "bones infection", "Osteomyelitides", "bone infections", "Bone Infections", "bone; infection", "bones infections", "Osteomyelitis NOS", "Infection in bone", "Infection of bone", "Infection;bone(s)", "Osteomyelitis, NOS", "Bone infection NOS", "OM - Osteomyelitis", "OSTM - Osteomyelitis", "chronic osteomyelitis", "Chronic osteomyelitis", "OSTEOMYELITIS CHRONIC", "Osteomyelitis;chronic", "osteomyelitis chronic", "Chronic Osteomyelitis", "Infection of bone NOS", "Osteomyelitis chronic", "chronic; osteomyelitis", "osteomyelitis; chronic", "osteomyelitis (disease)", "Osteomyelitis (disorder)", "Osteomyelitis chronic NOS", "osteomyelitis (diagnosis)", "unspecified osteomyelitis", "Unspecified osteomyelitis", "Chronic osteomyelitis, NOS", "Osteomyelitis, unspecified", "bone infection (diagnosis)", "Infection of bone (disorder)", "Pyogenic inflammation of bone", "Unspecified infection of bone", "Chronic osteomyelitis (disorder)", "chronic osteomyelitis (diagnosis)", "Pyogenic inflammation of bone, NOS", "Chronic osteomyelitis, site unspecified", "Unspecified osteomyelitis, site unspecified", "Unspecified infection of bone, site unspecified", "a bacterial infection of the bone or bone marrow", "Chronic osteomyelitis with or without periostitis", "Chronic or old osteomyelitis with or without mention of periostitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteomyelitis", "shortest_name_length": 13}
{"curie": "MONDO:0012018", "names": ["MSMA", "congenital myopathy 7A", "Myosin storage myopathy", "Myopathy, Myosin Storage", "Myosin storage myopathy (disorder)", "MYOPATHY, MYOSIN STORAGE (disorder)", "myopathy with lysis of type I myofibrils", "Autosomal dominant hyaline body myopathy", "autosomal dominant hyaline body myopathy", "myopathy with lysis of type 1 myofibrils", "MYOPATHY WITH LYSIS OF TYPE I MYOFIBRILS", "Myopathy, Hyaline Body, Autosomal Dominant", "MYOPATHY, HYALINE BODY, AUTOSOMAL DOMINANT", "myopathy, hyaline body, autosomal dominant", "MYOPATHY, MYOSIN STORAGE, AUTOSOMAL DOMINANT", "myopathy, myosin storage, autosomal dominant", "Myopathy, myosin storage, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy, myosin storage, autosomal dominant", "shortest_name_length": 4}
{"curie": "MONDO:0016351", "names": ["anti-HLA hyperimmunization"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anti-HLA hyperimmunization", "shortest_name_length": 26}
{"curie": "UMLS:C1134517", "names": ["NETK", "neuroepithelial tumor of the kidney", "Neuroepithelial Tumor of the Kidney", "Malignant Neuroepithelial Tumor of the Kidney", "peripheral primitive neuroectodermal tumor of the kidney", "Peripheral Primitive Neuroectodermal Tumor of the Kidney"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peripheral Primitive Neuroectodermal Tumor of the Kidney", "shortest_name_length": 4}
{"curie": "UMLS:C5555188", "names": ["Refractory Primary Peritoneal High Grade Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Primary Peritoneal High Grade Serous Adenocarcinoma", "shortest_name_length": 62}
{"curie": "MONDO:0045071", "names": ["mycosis fungoides variant", "Mycosis Fungoides Variant", "Mycosis fungoides and variants"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mycosis fungoides variant", "shortest_name_length": 25}
{"curie": "MONDO:0024677", "names": ["insuloma", "Insuloma", "INSULOMA", "Insulomas", "INSULINOMA", "Insulinoma", "insulinoma", "Insulinomas", "insulinomas", "Insulinoma NOS", "Insulinoma, NOS", "beta-Cell Tumor", "beta-cell tumor", "beta cell tumor", "Beta Cell Tumor", "beta Cell Tumor", "Tumor, beta-Cell", "tumor, beta-cell", "beta-Cell Tumors", "beta-cell tumors", "beta-cell adenoma", "Beta cell adenoma", "[M]Insulinoma NOS", "beta-Cell Adenoma", "tumors, beta-cell", "Beta-cell adenoma", "Tumors, beta-Cell", "islet cell adenoma", "Adenoma, beta-Cell", "adenoma, beta cell", "Beta Cell Neoplasm", "Adenoma, beta Cell", "beta-cell adenomas", "Islet cell adenoma", "adenoma, beta-cell", "beta-Cell Adenomas", "Adenomas, beta-Cell", "Insulinoma syndrome", "adenomas, beta-cell", "pancreas; insulinoma", "insulinoma; pancreas", "pancreatic insulinoma", "Pancreatic Insulinoma", "islet cell insulinoma", "Insulinoma (disorder)", "Pancreatic insulinoma", "pancreas; beta-cell tumor", "pancreas; tumor, beta-cell", "beta-cell; tumor, pancreas", "tumor; beta-cell, pancreas", "Pancreatic Beta Cell Tumor", "Beta Cell Tumor of Pancreas", "pancreas; adenoma, beta-cell", "beta-cell; adenoma, pancreas", "insulinoma; unspecified site", "adenoma; beta-cell, pancreas", "Beta Cell Neoplasm of Pancreas", "Beta Cell Tumor of the Pancreas", "Pancreatic Insulin Producing NET", "Pancreatic Insulin Producing Tumor", "beta-cell; tumor, unspecified site", "Beta Cell Neoplasm of the Pancreas", "tumor; beta-cell, unspecified site", "Insulin-Producing Islet Cell Tumor", "Insulin-Producing Islet Cell Neoplasm", "Pancreatic Insulin Producing Neoplasm", "insulinoma tumor suppressor GENE locus", "Insulin-Producing tumor of Islet cells", "Insulin-Producing Tumor of Islet Cells", "Insulin-Producing Neoplasm of Islet Cells", "Insulin-Producing Tumor of the Islet Cells", "PANCREAS, ISLET-CELL TUMOR, INSULIN-PRODUCING", "Insulin-Producing Neoplasm of the Islet Cells", "Pancreatic Insulin-Producing Neuroendocrine Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic insulinoma", "shortest_name_length": 8}
{"curie": "UMLS:C2984068", "names": ["Bladder Cancer by AJCC v7 Stage", "Bladder Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder Cancer by AJCC v7 Stage", "shortest_name_length": 31}
{"curie": "UMLS:C0333990", "names": ["Basal Cell Hyperplasia", "Basal cell hyperplasia", "basal cell hyperplasia", "Hyperplasia, basal cell", "Reserve cell hyperplasia", "Basal cell hyperplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Basal cell hyperplasia", "shortest_name_length": 22}
{"curie": "UMLS:C4683602", "names": ["Lugano Classification Stage III Childhood Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage III Childhood Hodgkin Lymphoma AJCC v8", "shortest_name_length": 66}
{"curie": "MONDO:0001786", "names": ["uterus; inflammation", "inflammation; uterus", "uterine inflammatory disease", "Uterine inflammatory disease", "inflammatory disease of uterus", "uterus; disorder, inflammatory", "inflammatory disease of the uterus", "Inflammatory disease of the uterus", "uterine disorders inflammatory disease", "Inflammatory disease of the uterus, NOS", "Unspecified inflammatory disease of uterus", "inflammatory disease of uterus (diagnosis)", "Inflammatory disease of uterus, unspecified", "Inflammatory disease of the uterus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine inflammatory disease", "shortest_name_length": 20}
{"curie": "UMLS:C0278882", "names": ["stage iii melanoma", "stage III melanoma", "melanoma stage iii", "melanoma, stage III", "stage III cutaneous melanoma", "cutaneous melanoma, stage III", "melanoma, cutaneous stage III", "Stage III Skin Melanoma AJCC v6", "Stage III Melanoma of Skin AJCC v6", "Stage III Cutaneous (Skin) Melanoma", "malignant melanoma of skin stage III", "Stage III Cutaneous Melanoma AJCC v6", "Stage III Melanoma of the Skin AJCC v6", "Stage III Malignant Skin Melanoma AJCC v6", "Stage III Malignant Melanoma of Skin AJCC v6", "Stage III Malignant Cutaneous Melanoma AJCC v6", "Malignant Melanoma (of Skin), Stage III AJCC v6", "Stage III Malignant Melanoma of the Skin AJCC v6", "malignant melanoma of skin stage III (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Cutaneous Melanoma AJCC v6", "shortest_name_length": 18}
{"curie": "UMLS:C5555194", "names": ["Platinum-Refractory Fallopian Tube Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Platinum-Refractory Fallopian Tube Carcinoma", "shortest_name_length": 44}
{"curie": "MONDO:0011325", "names": ["FANCF", "Fanconi anemia complementation group F", "Fanconi anemia, complementation group F", "Fanconi Anemia, Complementation Group F", "FANCONI ANEMIA, COMPLEMENTATION GROUP F", "Fanconi anemia complementation group type F", "Fanconi Anemia, complementation group type F", "Fanconi anemia complementation group F (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fanconi anemia complementation group F", "shortest_name_length": 5}
{"curie": "UMLS:C1334224", "names": ["Intermediate Soft Tissue Tumor", "Intermediate Soft Tissue Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intermediate Soft Tissue Neoplasm", "shortest_name_length": 30}
{"curie": "UMLS:C4725630", "names": ["Recurrent Monomorphic Epitheliotropic Intestinal T-cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Monomorphic Epitheliotropic Intestinal T-cell Lymphoma", "shortest_name_length": 64}
{"curie": "MONDO:0014376", "names": ["CSS9", "MRD27", "IDDMOH", "COFFIN-SIRIS SYNDROME 9", "Coffin-Siris syndrome 9", "autosomal dominant mental retardation 27", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 27", "mental retardation, autosomal dominant 27", "autosomal dominant intellectual disability 27", "intellectual disability, autosomal dominant 27", "mental retardation, autosomal dominant type 27", "intellectual disability, autosomal dominant type 27", "autosomal dominant non-syndromic intellectual disability 27", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH MICROCEPHALY AND WITH OR WITHOUT OCULAR MALFORMATIONS OR HYPOGONADOTROPIC HYPOGONADISM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 27", "shortest_name_length": 4}
{"curie": "UMLS:C3839433", "names": ["Nerve Sheath Tumor, NOS", "Hybrid Nerve Sheath Tumor", "Hybrid nerve sheath tumor", "Hybrid nerve sheath tumour", "Hybrid Nerve Sheath Neoplasm", "Hybrid Neurofibroma-Schwannoma", "Hybrid Schwannoma-Perineurioma", "Hybrid Neurofibroma-Perineurioma", "Nerve Sheath Tumor, Not Otherwise Specified", "Hybrid nerve sheath tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hybrid nerve sheath tumor", "shortest_name_length": 23}
{"curie": "UMLS:C5202818", "names": ["Non-Malignant Neoplasm", "Non-malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Malignant Neoplasm", "shortest_name_length": 22}
{"curie": "MONDO:0001143", "names": ["Paralytic squint", "paralytic squint", "Paralytic strabismus", "paralytic strabismus", "Neurogenic strabismus", "strabismus; paralytic", "Strabismus, paralytic", "paralytic; strabismus", "incomitant dissociation", "Incomitant dissociation", "Paralytic strabismus, NOS", "Paralytic strabismus (disorder)", "paralytic strabismus (diagnosis)", "Unspecified paralytic strabismus", "Paralytic strabismus, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paralytic strabismus", "shortest_name_length": 16}
{"curie": "MONDO:0021085", "names": ["gastric mass", "Gastric mass", "Gastric Tumor", "Gastric tumor", "tumor gastric", "Stomach Tumor", "gastric tumor", "GASTRIC TUMOR", "stomach tumor", "Stomach tumor", "gastric tumors", "stomach tumour", "stomach tumors", "Stomach tumour", "stomach tumours", "Stomach--Tumors", "Tumor of stomach", "stomach neoplasm", "neoplasm gastric", "tumor of stomach", "of stomach tumor", "gastric neoplasm", "Stomach Neoplasm", "Gastric Neoplasm", "Gastric neoplasm", "Tumor of Stomach", "Stomach Neoplasms", "Neoplasm, Gastric", "Neoplasm, Stomach", "gastric neoplasms", "stomach neoplasms", "Tumour of stomach", "Gastric Neoplasms", "Neoplasms, Gastric", "Neoplasms, Stomach", "Neoplasm of stomach", "neoplasm of stomach", "Neoplasm of Stomach", "Tumor of the Stomach", "tumor of the stomach", "Gastric neoplasm NOS", "cancer stomach tumors", "stomach tumor or cancer", "Neoplasm of the Stomach", "neoplasm of the stomach", "Neoplasm of the stomach", "Neoplasia of the stomach", "stomach neoplasm (disease)", "Neoplasm of stomach (disorder)", "neoplasm of stomach (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric neoplasm", "shortest_name_length": 12}
{"curie": "MONDO:0003893", "names": ["rete testis adenoma", "Rete Testis Adenoma", "ADENOMA, RETE TESTIS, BENIGN", "adenoma, rete testis, benign"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rete testis adenoma", "shortest_name_length": 19}
{"curie": "MONDO:0054849", "names": ["IBD29", "INFLAMMATORY BOWEL DISEASE 29", "inflammatory bowel disease 29"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory bowel disease 29", "shortest_name_length": 5}
{"curie": "MONDO:0012480", "names": ["Tndm2", "TNDM2", "diabetes mellitus, transient neonatal 2", "Diabetes mellitus, transient neonatal 2", "diabetes mellitus, transient neonatal, 2", "DIABETES MELLITUS, TRANSIENT NEONATAL, 2", "Diabetes Mellitus, Transient Neonatal, 2", "diabetes mellitus, transient neonatal, type 2", "Diabetes mellitus, transient neonatal 2 (disorder)", "DIABETES MELLITUS, TRANSIENT NEONATAL, 2 (disorder)", "ABCC8 transient neonatal diabetes mellitus (disease)", "transient neonatal diabetes mellitus (disease) caused by mutation in ABCC8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diabetes mellitus, transient neonatal, 2", "shortest_name_length": 5}
{"curie": "UMLS:C0855153", "names": ["relapsed primary mediastinal large B-cell lymphoma", "Relapsed Primary Mediastinal Large B-Cell Lymphoma", "Primary mediastinal large B-cell lymphoma recurrent", "Recurrent Primary Mediastinal Large B-Cell Lymphoma", "recurrent primary mediastinal large B-cell lymphoma", "Recurrent Mediastinal (Thymic) Large B-Cell Lymphoma", "recurrent mediastinal (thymic) large B-cell lymphoma", "Relapsed Primary Mediastinal (Thymic) Large B-Cell Lymphoma", "Recurrent Primary Mediastinal (Thymic) Large B-Cell Lymphoma", "Large B-cell lymphoma subtype primary mediastinal (Thymic) large B-cell lymphoma recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary mediastinal large B-cell lymphoma recurrent", "shortest_name_length": 50}
{"curie": "MONDO:0013663", "names": ["PAFAD", "Platelet-activating factor acetylhydrolase deficiency", "platelet-activating factor acetylhydrolase deficiency", "PLATELET-ACTIVATING FACTOR ACETYLHYDROLASE DEFICIENCY", "Platelet-Activating Factor Acetylhydrolase Deficiency", "platelet-activating factor acetylhydrolase deficiency (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "platelet-activating factor acetylhydrolase deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0023023", "names": ["Neonatal dacryocystitis", "neonatal dacryocystitis", "Neonatal Dacryocystitis", "neonatal; dacryocystitis", "dacryocystitis; neonatal", "Neonatal dacryocystitis, NOS", "Neonatal dacryocystitis (disorder)", "neonatal dacryocystitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal dacryocystitis", "shortest_name_length": 23}
{"curie": "MONDO:0033654", "names": ["MC4DN19", "mitochondrial complex 4 deficiency, nuclear type 19", "MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 19", "mitochondrial complex IV deficiency, nuclear type 19"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 4 deficiency, nuclear type 19", "shortest_name_length": 7}
{"curie": "MONDO:0100212", "names": ["IFAP syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IFAP syndrome", "shortest_name_length": 13}
{"curie": "UMLS:C1336327", "names": ["Stage II Thyroid Medullary Carcinoma", "Stage II Medullary Carcinoma of Thyroid", "Stage II Thyroid Gland Medullary Cancer", "Stage II Thyroid Gland Medullary Carcinoma", "Stage II Medullary Thyroid Gland Carcinoma", "Stage II Medullary Carcinoma of the Thyroid", "Stage II Medullary Carcinoma of Thyroid Gland", "Stage II Medullary Carcinoma of the Thyroid Gland", "Stage II Thyroid Gland Medullary Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Thyroid Gland Medullary Carcinoma AJCC v7", "shortest_name_length": 36}
{"curie": "MONDO:0013838", "names": ["COQ10D3", "PDSS2 coenzyme Q10 deficiency", "primary coenzyme Q10 deficiency 3", "coenzyme Q10 deficiency, primary, 3", "COENZYME Q10 DEFICIENCY, PRIMARY, 3", "coenzyme Q10 deficiency, primary, type 3", "coenzyme Q10 deficiency caused by mutation in PDSS2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coenzyme Q10 deficiency, primary, 3", "shortest_name_length": 7}
{"curie": "UMLS:C0275904", "names": ["cns tuberculosis", "CNS tuberculosis", "CNS TUBERCULOSIS", "Central Nervous System Tuberculosis", "central nervous system tuberculosis", "Tuberculosis, Central Nervous System", "Tuberculosis of central nervous system", "Tuberculosis of central nervous system NOS", "Tuberculosis of central nervous system, NOS", "central nervous system tuberculosis (diagnosis)", "Tuberculosis of central nervous system (disorder)", "Unspecified tuberculosis of central nervous system", "Unspecified tuberculosis of central nervous system, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tuberculosis, Central Nervous System", "shortest_name_length": 16}
{"curie": "MONDO:0022691", "names": ["Cerebelloolivary atrophy", "cerebello-olivary atrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebello-olivary atrophy", "shortest_name_length": 24}
{"curie": "MONDO:0004110", "names": ["Relapsed Hairy Cell Leukemia", "Hairy cell leukemia recurrent", "recurrent hairy cell leukemia", "Recurrent Hairy Cell Leukemia", "hairy cell leukemia, recurrent", "hairy cell leukemia in relapse", "refractory hairy cell leukemia", "Hairy cell leukaemia recurrent", "Refractory Hairy Cell Leukemia", "Hairy Cell Leukemia, Refractory", "hairy cell leukemia, refractory", "Hairy cell leukemia, in relapse", "leukemia, hairy cell, recurrent", "leukemia, hairy cell, refractory", "hairy cell leukemia in relapse (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "refractory hairy cell leukemia", "shortest_name_length": 28}
{"curie": "MONDO:0003399", "names": ["pineal body yolk sac tumor", "pineal region yolk sac tumor", "Pineal Region Yolk Sac Tumor", "pineal endodermal sinus tumor", "Pineal Endodermal Sinus Tumor", "yolk Sac tumor of pineal region", "pineal region yolk Sac neoplasm", "Yolk Sac Tumor of Pineal Region", "Pineal Region Yolk Sac neoplasm", "Pineal Region Yolk Sac Neoplasm", "Pineal Endodermal Sinus Neoplasm", "pineal endodermal sinus neoplasm", "Yolk Sac Tumor of the Pineal Region", "yolk Sac tumor of the pineal region", "pineal region endodermal sinus tumor", "Pineal Region Endodermal Sinus Tumor", "Pineal Region Endodermal Sinus Neoplasm", "Endodermal Sinus Tumor of Pineal Region", "pineal region endodermal sinus neoplasm", "endodermal sinus tumor of pineal region", "Endodermal Sinus Tumor of the Pineal Region", "endodermal sinus tumor of the pineal region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pineal region yolk sac tumor", "shortest_name_length": 26}
{"curie": "MONDO:0009727", "names": ["AO2", "DLCD", "AOII", "McAlister Dysplasia", "atelosteogenesis II", "Atelosteogenesis type 2", "atelosteogenesis type 2", "Atelosteogenesis, Type 2", "De La Chapelle Dysplasia", "De la Chapelle dysplasia", "atelosteogenesis, type 2", "Atelosteogenesis type II", "DE LA CHAPELLE DYSPLASIA", "atelosteogenesis type II", "Atelosteogenesis, Type II", "atelosteogenesis, type II", "De 50A Chapelle dysplasia", "ATELOSTEOGENESIS, TYPE II", "neonatal osseous dysplasia 1", "Neonatal Osseous Dysplasia I", "NEONATAL OSSEOUS DYSPLASIA I", "Neonatal osseous dysplasia 1", "neonatal osseous dysplasia type 1", "Neonatal osseous dysplasia type 1", "Atelosteogenesis type 2 (disorder)", "Atelosteogenesis de la Chapelle type", "Atelosteogenesis De La Chapelle Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atelosteogenesis type II", "shortest_name_length": 3}
{"curie": "MONDO:0012779", "names": ["CELIAC10", "CELIAC DISEASE, SUSCEPTIBILITY TO, 10", "celiac disease, susceptibility to, 10", "gluten-sensitive enteropathy, susceptibility to, 10", "GLUTEN-SENSITIVE ENTEROPATHY, SUSCEPTIBILITY TO, 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "celiac disease, susceptibility to, 10", "shortest_name_length": 8}
{"curie": "UMLS:C0013222", "names": ["Drug Use Disorder", "Drug use disorder", "Drug Use Disorders", "Disorder, Drug Use", "drug use disorders", "drug use disorders (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drug Use Disorders", "shortest_name_length": 17}
{"curie": "UMLS:C0276587", "names": ["AIDS with nutritional deficiency", "AIDS associated disorder - nutritional deficiency", "Nutritional deficiency with acquired immunodeficiency syndrome", "Nutritional deficiency with AIDS (acquired immunodeficiency syndrome)", "Nutritional deficiency with acquired immunodeficiency syndrome (disorder)", "Nutritional deficiency associated with acquired immunodeficiency syndrome", "Nutritional deficiency associated with acquired immunodeficiency syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nutritional deficiency with AIDS (acquired immunodeficiency syndrome)", "shortest_name_length": 32}
{"curie": "UMLS:C5418300", "names": ["Recurrent Anal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Anal Squamous Cell Carcinoma", "shortest_name_length": 38}
{"curie": "UMLS:C5420067", "names": ["Metastatic Intracranial Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Intracranial Malignant Neoplasm", "shortest_name_length": 42}
{"curie": "UMLS:C0860433", "names": ["Irreversible renal failure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Irreversible renal failure", "shortest_name_length": 26}
{"curie": "UMLS:C5205248", "names": ["Jejunal NET G2", "Jejunal Neuroendocrine Tumor G2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jejunal Neuroendocrine Tumor G2", "shortest_name_length": 14}
{"curie": "UMLS:C0855079", "names": ["Refractory Mixed Cellularity Hodgkin Lymphoma", "Hodgkin's disease mixed cellularity refractory", "Refractory Mixed Cellularity Hodgkin's Lymphoma", "Refractory Mixed Cellularity Classic Hodgkin Lymphoma", "Refractory Mixed Cellularity Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's disease mixed cellularity refractory", "shortest_name_length": 45}
{"curie": "MONDO:0011292", "names": ["ATOD", "ATOD1", "Baby eczema", "Canine atopy", "Eczema;atopic", "atopic eczema", "Atopic eczema", "Eczema atopic", "Atopic Eczema", "ECZEMA ATOPIC", "eczema; atopic", "Eczema, Atopic", "Eczema, atopic", "atopic; eczema", "eczema, atopic", "ECZEMA, ATOPIC", "allergic eczema", "Eczema allergic", "Allergic eczema", "allergy; eczema", "ECZEMA ALLERGIC", "eczema; allergy", "allergic; eczema", "eczema; allergic", "Eczema, allergic", "endogenous eczema", "DERMATITIS ATOPIC", "Atopic dermatitis", "atopic dermatitis", "Atopic Dermatitis", "Dermatitis;atopic", "Endogenous eczema", "Dermatitis atopic", "ATOPIC DERMATITIS", "besnier's prurigo", "Dermatitis, Atopic", "Dermatitis, atopic", "dermatitis, atopic", "DERMATITIS, ATOPIC", "Dermatitis;allergic", "Atopic Dermatitides", "allergy; dermatitis", "Allergic dermatitis", "Dermatitis allergic", "dermatitis; allergy", "allergic dermatitis", "DERMATITIS ALLERGIC", "dermatitis; allergic", "allergic; dermatitis", "Dermatitides, Atopic", "Dermatitis, Atopic, 1", "Constitutional eczema", "constitutional eczema", "DERMATITIS, ATOPIC, 1", "AD - Atopic dermatitis", "Atopic neurodermatitis", "constitutional; eczema", "atopic neurodermatitis", "Atopic Neurodermatitis", "Atopic dermatitis, NOS", "neurodermatitis atopic", "ECZEMA, CONSTITUTIONAL", "eczema; constitutional", "neurodermatitis; atopic", "Neurodermatitis, atopic", "Neurodermatitis, Atopic", "atopic; neurodermatitis", "Atopic Neurodermatitides", "Neurodermatitides, Atopic", "Atopic dermatitis, chronic", "atopic eczematous dermatitis", "Atopic dermatitis (disorder)", "Disseminated neurodermatitis", "Disseminated Neurodermatitis", "disseminated; neurodermatitis", "Neurodermatitis, Disseminated", "NEURODERMATITIS, DISSEMINATED", "neurodermatitis; disseminated", "Atopic dermatitis, unspecified", "Disseminated Neurodermatitides", "Allergic dermatitis (disorder)", "Neurodermatitides, Disseminated", "Atopic neurodermatitis (disorder)", "atopic neurodermatitis (diagnosis)", "atopic eczematous dermatitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermatitis, atopic", "shortest_name_length": 4}
{"curie": "MONDO:0019517", "names": ["WS2", "WS 2", "WS type 2", "Waardenburg syndrome type 2", "Waardenburg Syndrome Type 2", "Waardenburg syndrome type II", "Waardenburg Syndrome Type II", "WS type 2 Waardenburg syndrome type 2", "Waardenburg syndrome type 2 (disorder)", "Waardenburg syndrome type II (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Waardenburg syndrome type 2", "shortest_name_length": 3}
{"curie": "UMLS:C1335506", "names": ["Prostate Carcinoma Metastatic in the Lung", "Prostate Carcinoma Metastatic to the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Carcinoma Metastatic in the Lung", "shortest_name_length": 41}
{"curie": "MONDO:0004563", "names": ["Physiological Polycythemia", "Physiological polycythemia", "physiological polycythemia", "Physiological polycythaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "physiological polycythemia", "shortest_name_length": 26}
{"curie": "UMLS:C0031051", "names": ["pericementitis", "Pericementitis", "Pericementitides"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pericementitis", "shortest_name_length": 14}
{"curie": "MONDO:0004775", "names": ["iridocyclitis lens-induced", "lens-induced iridocyclitis", "Lens-induced iridocyclitis", "iridocyclitis; lens-induced", "Lens-induced iridocyclitis (disorder)", "Lens-induced iridocyclitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lens-induced iridocyclitis", "shortest_name_length": 26}
{"curie": "MONDO:0008450", "names": ["SPINAL ARACHNOIDITIS", "Spinal arachnoiditis", "spinal arachnoiditis", "Spinal Arachnoiditis", "arachnoiditis, spinal", "Arachnoiditis (spinal) NOS", "Familial spinal arachnoiditis", "Spinal arachnoiditis (disorder)", "Spinal tuberculous arachnoiditis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal arachnoiditis", "shortest_name_length": 20}
{"curie": "UMLS:C1710115", "names": ["Small Intestinal Villous Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Intestinal Villous Adenoma", "shortest_name_length": 32}
{"curie": "UMLS:C4527326", "names": ["Recurrent Extranodal Diffuse Large B-cell Lymphoma", "Recurrent Extranodal Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Extranodal Diffuse Large B-cell Lymphoma", "shortest_name_length": 50}
{"curie": "MONDO:0054780", "names": ["EL3", "elliptocytosis-3", "ELLIPTOCYTOSIS 3", "Elliptocytosis 3", "elliptocytosis 3", "anemia, neonatal hemolytic, fatal or near-fatal", "anemia, perinatal hemolytic, fatal or near-fatal", "ANEMIA, PERINATAL HEMOLYTIC, FATAL OR NEAR-FATAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "elliptocytosis 3", "shortest_name_length": 3}
{"curie": "MONDO:0060783", "names": ["classic CAH", "classic congenital adrenal hyperplasia", "Classic Congenital Adrenal Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "classic congenital adrenal hyperplasia", "shortest_name_length": 11}
{"curie": "MONDO:0003163", "names": ["cauda equina intradural extramedullary astrocytoma", "intradural extramedullary Cauda equina astrocytoma", "Intradural Extramedullary Cauda Equina Astrocytoma", "Intradural Extramedullary Astrocytoma of Cauda Equina", "intradural extramedullary astrocytoma of Cauda equina", "Intradural Extramedullary Astrocytoma of the Cauda Equina", "intradural extramedullary astrocytoma of the Cauda equina", "intradural extramedullary astrocytic tumor of the Cauda equina", "Intradural Extramedullary Astrocytic tumor of the Cauda Equina"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cauda equina intradural extramedullary astrocytoma", "shortest_name_length": 50}
{"curie": "UMLS:C0577598", "names": ["arm swell", "arm swollen", "Swollen;arm", "Swollen arm", "swollen arm", "Swelling arm", "arm swelling", "swelling arm", "arms swollen", "arms swelling", "arm; swelling", "arm swellings", "swelling; arm", "Swelling of arm", "swelling of arm", "Forelimb swelling", "upper arm swelling", "Swelling of upper arm", "swelling of upper arm", "Swelling of upper limb", "UPPER EXTREMITY SWELLING", "upper extremity swelling", "extremities swelling upper", "Swelling of upper extremities", "Swelling of upper arm (finding)", "Swelling of upper limb (finding)", "swelling of upper arm (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Swelling of arm", "shortest_name_length": 9}
{"curie": "UMLS:C2711180", "names": ["Influenza due to Influenza A virus", "Influenza caused by Influenza A virus", "Influenza caused by Influenza A virus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Influenza due to Influenza A virus", "shortest_name_length": 34}
{"curie": "MONDO:0012763", "names": ["EIG6", "ECA6", "CACNA1H childhood absence epilepsy", "susceptibility to childhood absence epilepsy 6", "epilepsy, childhood absence, susceptibility to, 6", "EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 6", "epilepsy, idiopathic generalized, susceptibility to, 6", "EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 6", "epilepsy, childhood absence, susceptibility to, type 6", "childhood absence epilepsy caused by mutation in CACNA1H"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, childhood absence, susceptibility to, 6", "shortest_name_length": 4}
{"curie": "MONDO:0007289", "names": ["CTRCT13", "cataract 13 with adult i phenotype", "cataract 13 with adult I phenotype", "CATARACT 13 WITH ADULT i PHENOTYPE", "cataract 13 with ADULT I phenotype"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 13 with adult I phenotype", "shortest_name_length": 7}
{"curie": "MONDO:0015538", "names": ["IDCT", "indeterminate cell histiocytosis", "Indeterminate cell histiocytosis", "Indeterminate Cell Histiocytosis", "Indeterminate Dendritic Cell Tumor", "indeterminate dendritic cell tumor", "Indeterminate dendritic cell tumor", "indeterminate Dendritic cell tumor", "Indeterminate dendritic cell tumour", "Indeterminate dendritic cell neoplasm", "Indeterminate dendritic cell neoplasm (disorder)", "Indeterminate dendritic cell neoplasm (diagnosis)", "Indeterminate dendritic cell tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "indeterminate dendritic cell tumor", "shortest_name_length": 4}
{"curie": "UMLS:C1963757", "names": ["Dopamine dysregulation syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dopamine dysregulation syndrome", "shortest_name_length": 31}
{"curie": "MONDO:0008747", "names": ["ROCA", "OCA3", "Xanthism", "XANTHISM", "Rufous OCA", "Albinism 3", "rufous OCA", "albinism 3", "Albinism III", "ALBINISM III", "Rufous albinism", "Red-skin albinism", "Rufous albinism (disorder)", "Red oculocutaneous albinism", "TYRP1 oculocutaneous albinism", "rufous oculocutaneous albinism", "oculocutaneous albinism type 3", "Oculocutaneous albinism type 3", "Rufous oculocutaneous albinism", "Rufous Oculocutaneous Albinism", "RUFOUS OCULOCUTANEOUS ALBINISM", "oculocutaneous albinism, type 3", "albinism, oculocutaneous, type 3", "Albinism, oculocutaneous, type 3", "xanthous oculocutaneous albinism", "oculocutaneous albinism type III", "Xanthous oculocutaneous albinism", "Oculocutaneous Albinism, Type III", "OCULOCUTANEOUS ALBINISM, TYPE III", "Albinism, Oculocutaneous, Type III", "albinism, oculocutaneous, type III", "ALBINISM, OCULOCUTANEOUS, TYPE III", "[OBSOLETE] Oculocutaneous albinism type 3", "oculocutaneous albinism type 3 (diagnosis)", "oculocutaneous albinism caused by mutation in TYRP1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculocutaneous albinism type 3", "shortest_name_length": 4}
{"curie": "UMLS:C1515296", "names": ["Testicular Sertoli Cell Tumor, Lipid Rich Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular Sertoli Cell Tumor, Lipid Rich Variant", "shortest_name_length": 49}
{"curie": "MONDO:0015174", "names": ["autoimmune enteropathy type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune enteropathy type 3", "shortest_name_length": 29}
{"curie": "UMLS:C5238498", "names": ["Signet-Ring Cell/Histiocytoid Carcinoma", "Signet Ring Cell/Histiocytoid Carcinoma", "Signet=Ring Cell/Histiocytoid Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Signet Ring Cell/Histiocytoid Carcinoma", "shortest_name_length": 39}
{"curie": "MONDO:0014885", "names": ["HPS10", "HERMANSKY-PUDLAK SYNDROME 10", "Hermansky-Pudlak syndrome 10", "AP3D1 Hermansky-Pudlak syndrome", "Hermansky-Pudlak syndrome type 10", "Hermansky-Pudlak syndrome 10; HPS10", "Hermansky-Pudlak syndrome caused by mutation in AP3D1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hermansky-Pudlak syndrome 10", "shortest_name_length": 5}
{"curie": "UMLS:C3272616", "names": ["Intestinal NET G2", "Intestinal Neuroendocrine Tumor G2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal Neuroendocrine Tumor G2", "shortest_name_length": 17}
{"curie": "UMLS:C0151609", "names": ["EDEMA SCROTUM", "scrotal edema", "scrotum edema", "Edema scrotum", "EDEMA SCROTAL", "Scrotum Edema", "Scrotal edema", "SCROTAL EDEMA", "SCROTUM EDEMA", "Edema scrotal", "OEDEMA SCROTUM", "Oedema scrotum", "edema; scrotum", "Scrotal oedema", "scrotum; edema", "Oedema scrotal", "Edema of scrotum", "Oedema of scrotum", "Edema of scrotum (disorder)", "scrotal edema (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Edema of scrotum", "shortest_name_length": 13}
{"curie": "MONDO:0018563", "names": ["agenesis; toe", "adactyly of foot", "Congenital absence of toe", "congenital absence of toe", "congenital absence of toes", "absence; toe(s), congenital", "toe (toes); absence, congenital", "TOE DEFORMITY CONGENITAL ABSENCE", "Congenital absence of toe (disorder)", "congenital absence of toe (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adactyly of foot", "shortest_name_length": 13}
{"curie": "UMLS:C2212604", "names": ["Bladder Alveolar Rhabdomyosarcoma", "alveolar rhabdomyosarcoma of bladder", "alveolar rhabdomyosarcoma of bladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alveolar rhabdomyosarcoma of bladder", "shortest_name_length": 33}
{"curie": "MONDO:0003912", "names": ["Ciliary body melanoma", "ciliary body melanoma", "Ciliary Body Melanoma", "melanoma of ciliary body", "Melanoma of Ciliary Body", "Melanoma of the Ciliary Body", "melanoma of the ciliary body", "melanoma of the Ciliary body", "malignant ciliary body melanoma", "ciliary body melanoma (disease)", "ciliary body malignant melanoma", "Ciliary Body Malignant Melanoma", "Malignant melanoma of ciliary body", "melanoma (disease) of ciliary body", "malignant melanoma of ciliary body", "Malignant Melanoma of Ciliary Body", "Malignant Melanoma of the Ciliary Body", "malignant melanoma of the ciliary body", "eye neoplasm malignant melanoma ciliary body", "Malignant melanoma of ciliary body (disorder)", "eye neoplasm malignant melanoma ciliary body (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant ciliary body melanoma", "shortest_name_length": 21}
{"curie": "UMLS:C3502495", "names": ["PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND SEX REVERSAL", "Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and Sex Reversal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and Sex Reversal", "shortest_name_length": 81}
{"curie": "MONDO:0001476", "names": ["COI", "coloboma", "COLOBOMA", "Coloboma", "colobomas", "Colobomas", "colobomata", "Colobomata", "coloboma eye", "Coloboma NOS", "Eye coloboma", "Notched pupil", "Coloboma of eye", "Ocular Coloboma", "coloboma of eye", "ocular coloboma", "Ocular coloboma", "Ocular Colobomas", "Coloboma, Ocular", "Ocular colobomas", "COLOBOMA, OCULAR", "Colobomas, Ocular", "coloboma of macula", "coloboma of the eye", "Coloboma of the Eye", "congenital coloboma", "Coloboma of eye, NOS", "Ocular coloboma, NOS", "congenital ocular coloboma", "Congenital ocular coloboma", "coloboma (physical finding)", "congenital coloboma (diagnosis)", "Congenital ocular coloboma, NOS", "Coloboma of iris, choroid and retina", "COLOBOMA, OCULAR, AUTOSOMAL DOMINANT", "Coloboma of iris, retina, and choroid", "COLOBOMA OF IRIS, CHOROID, AND RETINA", "Coloboma of iris, choroid, and retina", "Coloboma Of Iris, Choroid, And Retina", "Congenital ocular coloboma (disorder)", "Congenital ocular coloboma (diagnosis)", "COI - Coloboma of iris, choroid and retina", "congenital anomalies of eye ocular coloboma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coloboma", "shortest_name_length": 3}
{"curie": "UMLS:C2367273", "names": ["Methicillin-Sensitive Staphylococcus aureus Infection", "Methicillin-sensitive Staphylococcus aureus infection", "methicillin-susceptible Staphylococcus aureus infection", "methicillin susceptible Staphylococcus aureus infection", "Infection by methicillin sensitive Staphylococcus aureus", "Infection by methicillin susceptible Staphylococcus aureus", "Infection caused by methicillin sensitive Staphylococcus aureus", "Infection caused by methicillin susceptible Staphylococcus aureus", "methicillin-susceptible Staphylococcus aureus infection (diagnosis)", "Infection caused by methicillin susceptible Staphylococcus aureus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infection by methicillin sensitive Staphylococcus aureus", "shortest_name_length": 53}
{"curie": "MONDO:0015837", "names": ["Unicervical bicornuate uterus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unicervical bicornuate uterus", "shortest_name_length": 29}
{"curie": "MONDO:0018906", "names": ["Brill-Symmers", "Nodular lymphoma", "nodular lymphoma", "Nodular Lymphoma", "lymphoma; nodular", "Nodular Lymphomas", "nodular; lymphoma", "Lymphoma, Nodular", "Lymphomas, Nodular", "Follicular Lymphoma", "follicular lymphoma", "Follicular lymphoma", "lymphoma follicular", "lymphoma, follicular", "lymphoma; follicular", "Follicular lymphomas", "Follicular Lymphomas", "follicular lymphomas", "Lymphoma, Follicular", "nodular lymphosarcoma", "Brill-Symmers disease", "Brill-Symmers Disease", "Nodular lymphosarcoma", "Brill Symmers Disease", "Lymphomas, Follicular", "Brill-Symmers' disease", "Disease, Brill-Symmers", "lymphosarcoma follicular", "Follicular lymphosarcoma", "Brill - Symmers' disease", "Follicle Center Lymphoma", "follicle center lymphoma", "giant follicular lymphoma", "lymphosarcoma; follicular", "Giant follicular lymphoma", "Giant Follicular Lymphoma", "follicular; lymphosarcoma", "Lymphoma, Giant Follicular", "nodular malignant lymphoma", "Giant Follicular Lymphomas", "Nodular malignant lymphoma", "Follicular Lymphoma, Giant", "Malignant lymphoma, nodular", "Nodular lymphoma (disorder)", "Follicular Lymphomas, Giant", "Lymphomas, Giant Follicular", "follicular; germinoblastoma", "Germinoblastoma, follicular", "germinoblastoma; follicular", "LEUKEMIA/LYMPHOMA, B-CELL, 2", "Nodular lymphocytic lymphoma", "Nodular (follicular) lymphoma", "Lymphocytic lymphoma, nodular", "nodular; lymphoma, lymphocytic", "lymphoma; nodular, lymphocytic", "giant follicular lymphosarcoma", "lymphocytic; lymphoma, nodular", "Giant follicular lymphosarcoma", "lymphoma; lymphocytic, nodular", "Malignant lymphoma, follicular", "lymphoma, follicular, malignant", "Follicular Non-Hodgkin Lymphoma", "follicular lymphoma (diagnosis)", "LYMPHOMA, FOLLICULAR, MALIGNANT", "follicular centre cell lymphoma", "follicular non-Hodgkin lymphoma", "Follicular Centre Cell Lymphoma", "Follicular non-Hodgkin lymphoma", "lymphoma, follicular centre cell", "Nodular and Follicular Lymphomas", "Malignant lymphoma, nodular, NOS", "Lymphoma, Follicular Centre Cell", "Follicular lymphoma, unspecified", "nodular lymphosarcoma (diagnosis)", "Follicular Non-Hodgkin's Lymphoma", "Follicular non-Hodgkin's lymphoma", "follicular non-Hodgkin's lymphoma", "Malignant lymphoma, follicular NOS", "Malignant lymphoma, follicle center", "Malignant lymphoma, follicular, NOS", "Malignant lymphoma, follicle centre", "Follicular low grade B-cell lymphoma", "nodular malignant lymphoma (diagnosis)", "Malignant lymphoma, lymphocytic, nodular", "giant follicular lymphosarcoma (diagnosis)", "Follicular [nodular] non-Hodgkin's lymphoma", "Follicular non-Hodgkin's lymphoma (disorder)", "Malignant lymphoma, lymphocytic, nodular, NOS", "Follicular lymphoma (morphologic abnormality)", "Follicular non-Hodgkin's lymphoma, unspecified", "malignant neoplasm nodular lymphoma follicular", "Malignant lymphoma, follicle centre, follicular", "Malignant lymphoma, follicle center, follicular", "Follicular low grade B-cell lymphoma (disorder)", "Follicular low grade B-cell lymphoma (diagnosis)", "Malignant lymphoma, centroblastic-centrocytic, follicular", "follicular malignant lymphoma - centroblastic-centrocytic", "[M]Malignant lymphoma, centroblastic-centrocytic, follicular", "malignant neoplasm lymphoma follicular - centroblastic-centrocytic", "Malignant lymphoma, centroblastic-centrocytic, follicular (disorder)", "follicular malignant lymphoma - centroblastic-centrocytic (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "follicular lymphoma", "shortest_name_length": 13}
{"curie": "MONDO:0016727", "names": ["EVN", "extraventricular neurocytoma", "Extraventricular Neurocytoma", "Extraventricular neurocytoma", "Extraventricular neurocytoma (disorder)", "Extraventricular Neurocytoma (WHO Grade 2)", "extraventricular neurocytoma (WHO grade II)", "Extraventricular Neurocytoma (WHO Grade II)", "Extraventricular neurocytoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extraventricular neurocytoma", "shortest_name_length": 3}
{"curie": "MONDO:0012083", "names": ["DFNA28", "autosomal dominant deafness 28", "Deafness, Autosomal Dominant 28", "deafness, autosomal dominant 28", "DEAFNESS, AUTOSOMAL DOMINANT 28", "deafness, autosomal dominant type 28", "autosomal dominant nonsyndromic deafness 28", "GRHL2 autosomal dominant nonsyndromic deafness", "autosomal dominant nonsyndromic hearing loss 28", "autosomal dominant nonsyndromic deafness type 28", "autosomal dominant nonsyndromic deafness caused by mutation in GRHL2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 28", "shortest_name_length": 6}
{"curie": "UMLS:C0340214", "names": ["Tracheal Fistula", "fistula; trachea", "Tracheal fistula", "trachea; fistula", "tracheal fistula", "fistulas tracheal", "Tracheal fistula (disorder)", "tracheal fistula (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tracheal fistula", "shortest_name_length": 16}
{"curie": "UMLS:C0021568", "names": ["Bug bites", "Insect bite/sting", "stings bites insect", "insect stings bites", "insect bites stings", "bites insect stings", "Insect Bites and Stings"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Insect Bites and Stings", "shortest_name_length": 9}
{"curie": "UMLS:C0272334", "names": ["Hereditary Factor XII Deficiency", "Hereditary Hageman Factor Deficiency", "Hereditary factor XII deficiency disease", "Hereditary Factor XII Deficiency Disease", "Hereditary Hageman factor deficiency disease", "Hereditary factor XII deficiency disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hereditary factor XII deficiency disease", "shortest_name_length": 32}
{"curie": "MONDO:0011781", "names": ["CPD2", "HDL4", "SCA17", "OPCA5", "SCA 17", "OPCA V", "SPINOCEREBELLAR ATAXIA 17", "Huntington disease-like 4", "Huntington Disease-Like 4", "Spinocerebellar Ataxia 17", "HUNTINGTON DISEASE-LIKE 4", "spinocerebellar ataxia 17", "Cpd, Late-Onset Recessive Type", "Spinocerebellar Ataxia Type 17", "CPD, late-onset recessive type", "OLIVOPONTOCEREBELLAR ATROPHY V", "olivopontocerebellar atrophy 5", "HDL4 Huntington Disease-Like 4", "Olivopontocerebellar Atrophy V", "spinocerebellar ataxia type 17", "olivopontocerebellar atrophy V", "Spinocerebellar ataxia type 17", "SCA17 Spinocerebellar Ataxia 17", "Cerebelloparenchymal Disorder II", "cerebelloparenchymal disorder II", "CEREBELLOPARENCHYMAL DISORDER II", "olivopontocerebellar atrophy type 5", "Spinocerebellar ataxia type 17 (disorder)", "OPCA with dementia and extrapyramidal signs", "OPCA with Dementia and Extrapyramidal Signs"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia type 17", "shortest_name_length": 4}
{"curie": "MONDO:0005615", "names": ["plasmocytoma", "Plasmocytoma", "plasmacytoma", "Plasmacytoma", "PLASMACYTOMA", "plasmocytomas", "Plasmocytomas", "plasmacytomas", "Plasmacytomas", "solitary myeloma", "Solitary myeloma", "Plasmacytoma NOS", "Plasma Cell Tumor", "myeloma; solitary", "myeloma, solitary", "bone plasmacytoma", "solitary; myeloma", "Plasmacytoma, NOS", "Plasma cell tumor", "Myeloma, solitary", "plasma cell tumor", "Monostotic myeloma", "Plasma cell tumour", "myeloma - solitary", "plasma cell tumors", "Tumor, Plasma Cell", "tumor; plasma cell", "plasma cell; tumor", "PLASMA CELL TUMORS", "Plasma Cell Tumors", "Myeloma - solitary", "Tumors, Plasma Cell", "myeloma; monostotic", "monostotic; myeloma", "solitary plasmacytoma", "Solitary Plasmacytoma", "Solitary plasmacytoma", "plasma cell neoplasms", "plasmacytomas solitary", "Plasmacytoma of animal", "malignant plasmacytoma", "anaplastic plasmacytoma", "Plasmacytoma (disorder)", "Plasmacytoma - disorder", "Solitary plasmacytoma NOS", "myeloma; monostotic, plasma cell", "monostotic; myeloma, plasma cell", "Plasmacytoma of animal (disorder)", "malignant plasmacytoma (diagnosis)", "Plasmacytoma (morphologic abnormality)", "anaplastic skeletal plasmacytoma (type)", "extramedullary anaplastic plasmacytoma (type)", "anaplastic solitary extramedullary plasmacytoma of the cecum (type)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "plasmacytoma", "shortest_name_length": 12}
{"curie": "MONDO:0015020", "names": ["MRT59", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 59", "mental retardation, autosomal recessive 59", "mental retardation, autosomal recessive type 59", "intellectual disability, autosomal recessive 59", "intellectual disability, autosomal recessive type 59", "autosomal recessive intellectual developmental disorder 59", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 59", "IMPA1 autosomal recessive non-syndromic intellectual disability", "autosomal recessive non-syndromic intellectual disability caused by mutation in IMPA1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 59", "shortest_name_length": 5}
{"curie": "MONDO:0024973", "names": ["ABPE", "Fog fever", "Fog Fever", "Fever, Fog", "fever, Fog", "bovine pulmonary adenomatosis", "bovine pulmonary Adenomatoses", "pulmonary Adenomatoses, bovine", "adenomatosis, bovine pulmonary", "pulmonary adenomatosis, bovine", "Adenomatoses, bovine pulmonary", "adenomatosis, pulmonary, bovine", "emphysema, acute bovine pulmonary", "Emphysema, Acute Bovine Pulmonary", "Bovine atypical interstitial pneumonia", "Atypical Interstitial Pneumonia of Cattle", "atypical interstitial pneumonia of cattle", "Atypical interstitial pneumonia in cattle", "Atypical interstitial pneumonia of cattle", "Acute bovine pulmonary emphysema and edema", "Acute bovine pulmonary emphysema AND edema", "Acute bovine pulmonary emphysema AND oedema", "Acute bovine pulmonary emphysema and oedema", "pneumonia, atypical interstitial, of cattle", "Pneumonia, Atypical Interstitial, of Cattle", "Atypical interstitial pneumonia of cattle (disorder)", "Acute bovine pulmonary emphysema AND edema (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pneumonia, atypical interstitial, of cattle", "shortest_name_length": 4}
{"curie": "UMLS:C5446864", "names": ["Locally Advanced Pleural Malignant Mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Pleural Malignant Mesothelioma", "shortest_name_length": 47}
{"curie": "UMLS:C0266752", "names": ["twin placenta", "placenta twin", "Twin placenta", "Placenta, twin", "placenta twins", "Placenta duplex", "Placenta Duplex", "duplex; placenta", "placenta; duplex", "Bilobate placenta", "bilobate placenta", "Bilobate Placenta", "Bipartite placenta", "Twin placenta, NOS", "Placenta, bilobate", "Placenta Bipartita", "Bipartite Placenta", "Placenta bipartita", "placenta; bipartita", "bipartita; placenta", "Twin placenta (disorder)", "Bilobate placenta (disorder)", "Bilobate Chorionic Surface Shape"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bilobate placenta", "shortest_name_length": 13}
{"curie": "UMLS:C4527071", "names": ["Pathologic Stage III Merkel Cell Carcinoma AJCC v8", "Pathologic Stage III Neuroendocrine Carcinoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage III Merkel Cell Carcinoma AJCC v8", "shortest_name_length": 50}
{"curie": "MONDO:0013870", "names": ["CDG2K", "CDGIIk", "CDG-IIk", "CDG IIk", "CDGIIdk", "TMEM165-CDG", "CDG syndrome type IIk", "TMEM165-CDG (CDG-IIk)", "TMEM165-congenital disorder of glycosylation", "Congenital disorder of glycosylation type 2k", "congenital disorder of glycosylation type 2k", "congenital disorder of glycosylation type IIk", "Congenital disorder of glycosylation type IIk", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIk", "congenital disorder of glycosylation, type IIk", "Carbohydrate deficient glycoprotein syndrome type 2k", "Carbohydrate deficient glycoprotein syndrome type IIk", "carbohydrate deficient glycoprotein syndrome type IIk", "Transmembrane protein 165 congenital disorder of glycosylation", "Carbohydrate deficient glycoprotein syndrome type 2k (disorder)", "TMEM165-CDG - transmembrane protein 165 congenital disorder of glycosylation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "TMEM165-congenital disorder of glycosylation", "shortest_name_length": 5}
{"curie": "MONDO:0012192", "names": ["paca", "PACA", "Pancreatic and Cerebellar Agenesis", "pancreatic and cerebellar agenesis", "PANCREATIC AND CEREBELLAR AGENESIS", "Pancreatic and cerebellar agenesis", "Diabetes Mellitus, Permanent Neonatal, with Cerebellar Agenesis", "diabetes mellitus, permanent neonatal, with cerebellar agenesis", "DIABETES MELLITUS, PERMANENT NEONATAL, WITH CEREBELLAR AGENESIS", "permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome", "Permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0012450", "names": ["SCA28", "SPINOCEREBELLAR ATAXIA 28", "spinocerebellar ataxia 28", "Spinocerebellar ataxia 28", "spinocerebellar ataxia type 28", "Spinocerebellar ataxia type 28", "SCA28 Spinocerebellar ataxia 28", "Spinocerebellar ataxia type 28 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia type 28", "shortest_name_length": 5}
{"curie": "MONDO:0010047", "names": ["SPG5A", "Spastic Paraplegia 5A", "spastic paraplegia 5A", "spastic paraplegia type 5A", "hereditary spastic paraplegia 5A", "spastic paraplegia type 5B, recessive", "Spastic paraplegia type 5B, recessive", "hereditary spastic paraplegia type 5A", "autosomal recessive spastic paraplegia", "autosomal recessive spastic paraplegia 5A", "spastic paraplegia 5A, autosomal recessive", "Spastic Paraplegia 5a, Autosomal Recessive", "SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE", "autosomal recessive spastic paraplegia type 5A", "Autosomal recessive spastic paraplegia type 5A", "SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE (disorder)", "familial spastic paraplegia autosomal recessive type 5a", "Autosomal recessive spastic paraplegia type 5A (disorder)", "Autosomal recessive spastic paraplegia type 5A (diagnosis)", "CYP7B1 pure or complex autosomal recessive spastic paraplegia", "pure or complex autosomal recessive spastic paraplegia caused by mutation in CYP7B1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 5A", "shortest_name_length": 5}
{"curie": "MONDO:0700165", "names": ["canine thyroid gland medullary carcinoma", "Canine Thyroid Gland Medullary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canine thyroid gland medullary carcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0020528", "names": ["ACTH-dependent CS", "overproduction of ACTH", "Overproduction of ACTH", "pituitary Cushing disease", "pituitary Cushing syndrome", "pituitary Cushing diseases", "Pituitary ACTH Hypersecretion", "ACTH hypersecretion, pituitary", "ACTH-dependent Cushing syndrome", "ACTH-dependent Cushing's syndrome", "pituitary-dependent Cushing disease", "pituitary-dependent Cushing's disease", "Corticotropin-dependent Cushing syndrome", "corticotropin-dependent Cushing syndrome", "adrenocorticotropic hormone, inappropriate secretion", "adrenocorticotropic hormone-dependent Cushing syndrome", "Adrenocorticotropic hormone-dependent Cushing syndrome", "adrenocorticotropic hormone-dependent Cushing's syndrome", "Cushing's syndrome adrenocorticotropic hormone-dependent", "Adrenocorticotropic hormone (ACTH)-dependent Cushing syndrome", "Adrenocorticotropic hormone (ACTH)-dependent Cushing's syndrome", "Adrenocorticotropic hormone-dependent Cushing syndrome (disorder)", "adrenocorticotropic hormone-dependent Cushing's syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ACTH-dependent Cushing syndrome", "shortest_name_length": 17}
{"curie": "UMLS:C3273139", "names": ["Extrahepatic Bile Duct NET", "Extrahepatic Bile Duct Neuroendocrine Tumor", "Extrahepatic Bile Duct Well Differentiated Endocrine Tumor", "Extrahepatic Bile Duct Well Differentiated Endocrine Tumor/Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extrahepatic Bile Duct Neuroendocrine Tumor", "shortest_name_length": 26}
{"curie": "UMLS:C2217036", "names": ["Stage IIB Colon Cancer", "Stage IIB Colon Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Colon Cancer AJCC v7", "shortest_name_length": 22}
{"curie": "UMLS:C4521870", "names": ["Stage IV Ampulla of Vater Cancer", "Stage IV Ampulla of Vater Cancer AJCC v8", "Stage IV Ampulla of Vater Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Ampulla of Vater Cancer AJCC v8", "shortest_name_length": 32}
{"curie": "MONDO:0012211", "names": ["CDGIf", "CDG1F", "CDG-If", "CDG If", "CDG 1F", "MPDU1-CDG", "MPDU1-CDG (CDG-If)", "CDG syndrome type If", "Mannose-P-dolichol utilisation defect 1", "congenital disorder of glycosylation 1f", "Mannose-P-dolichol utilization defect 1", "congenital disorder of glycosylation If", "MPDU1-congenital disorder of glycosylation", "congenital disorder of glycosylation type If", "congenital disorder of glycosylation type 1f", "Congenital Disorder of Glycosylation Type If", "Congenital disorder of glycosylation type 1F", "Congenital disorder of glycosylation type If", "Congenital disorder of glycosylation type 1f", "congenital disorder of glycosylation, type If", "Congenital Disorder of Glycosylation, Type IF", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE If", "carbohydrate-deficient glycoprotein syndrome type 1F", "Carbohydrate deficient glycoprotein syndrome type If", "carbohydrate deficient glycoprotein syndrome type If", "Congenital disorder of glycosylation type 1f (disorder)", "congenital disorder of glycosylation type If (diagnosis)", "MPDU1-CDG - mannose-P-dolichol utilization defect 1 - congenital disorder of glycosylation", "MPDU1-CDG - mannose-P-dolichol utilisation defect 1 - congenital disorder of glycosylation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MPDU1-congenital disorder of glycosylation", "shortest_name_length": 5}
{"curie": "UMLS:C0596263", "names": ["Oncogenesis", "Oncogeneses", "Tumorigeneses", "Tumorigenesis", "carcinogenesis", "Carcinogeneses", "Carcinogenesis", "Cancer Induction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carcinogenesis", "shortest_name_length": 11}
{"curie": "UMLS:C0270730", "names": ["MPTP Poisoning", "Poisoning, MPTP", "MPTP-induced parkinsonism", "MPTP Induced Parkinsonism", "MPTP-Induced Parkinsonism", "Parkinsonism, MPTP-Induced", "MPTP Neurotoxicity Syndrome", "Neurotoxicity Syndrome, MPTP", "MPTP Neurotoxicity Syndromes", "Neurotoxicity Syndromes, MPTP", "Methylphenyltetrahydropyridine-induced parkinsonism", "Poisoning, 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine", "MPTP - Methylphenyltetrahydropyridine-induced parkinsonism", "1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced parkinsonism", "1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced parkinsonism", "1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced parkinsonism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MPTP Poisoning", "shortest_name_length": 14}
{"curie": "UMLS:C0861556", "names": ["Relapsed Mouth Epidermoid Carcinoma", "Recurrent Mouth Epidermoid Carcinoma", "Relapsed Mouth Squamous Cell Carcinoma", "Relapsed Epidermoid Carcinoma of Mouth", "Recurrent Epidermoid Carcinoma of Mouth", "Recurrent Mouth Squamous Cell Carcinoma", "Relapsed Oral Cavity Epidermoid Carcinoma", "Relapsed Squamous Cell Carcinoma of Mouth", "Recurrent Oral Cavity Epidermoid Carcinoma", "Recurrent Squamous Cell Carcinoma of Mouth", "Relapsed Epidermoid Carcinoma of the Mouth", "Recurrent Epidermoid Carcinoma of the Mouth", "Relapsed Oral Cavity Squamous Cell Carcinoma", "Relapsed Epidermoid Carcinoma of Oral Cavity", "Recurrent Epidermoid Carcinoma of Oral Cavity", "Recurrent Oral Cavity Squamous Cell Carcinoma", "Relapsed Squamous Cell Carcinoma of the Mouth", "Recurrent Squamous Cell Carcinoma of the Mouth", "Relapsed Squamous Cell Carcinoma of Oral Cavity", "Relapsed Epidermoid Carcinoma of the Oral Cavity", "Recurrent Squamous Cell Carcinoma of Oral Cavity", "Recurrent Epidermoid Carcinoma of the Oral Cavity", "Relapsed Squamous Cell Carcinoma of the Oral Cavity", "Squamous cell carcinoma of the oral cavity recurrent", "Recurrent Squamous Cell Carcinoma of the Oral Cavity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Squamous cell carcinoma of the oral cavity recurrent", "shortest_name_length": 35}
{"curie": "MONDO:0009051", "names": ["cutaneous photosensitivity and colitis, lethal", "Cutaneous photosensitivity and colitis, lethal", "CUTANEOUS PHOTOSENSITIVITY AND COLITIS, LETHAL", "cutaneous photosensitivity-lethal colitis syndrome", "early cutaneous photosensitivity and severe colitis", "Early cutaneous photosensitivity and severe colitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous photosensitivity-lethal colitis syndrome", "shortest_name_length": 46}
{"curie": "UMLS:C0151795", "names": ["Injection site erosion", "INJECTION SITE NECROSIS", "NECROSIS INJECTION SITE", "Necrosis injection site", "Injection site necrosis", "injection site disorder necrosis", "Injection site necrosis (disorder)", "Injection site necrosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site necrosis", "shortest_name_length": 22}
{"curie": "MONDO:0020172", "names": ["skin of eyelid tumor", "tumor of skin of eyelid", "skin of eyelid neoplasm", "palpebral epidermal tumor", "neoplasm of skin of eyelid", "Neoplasm of skin of eyelid", "skin of eyelid neoplasm (disease)", "Neoplasm of skin of eyelid (disorder)", "neoplasm of skin of eyelid (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "palpebral epidermal tumor", "shortest_name_length": 20}
{"curie": "UMLS:C1449646", "names": ["Primary Peritonitis", "Primary peritonitis", "Peritonitis, Primary", "Primary peritonitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Peritonitis", "shortest_name_length": 19}
{"curie": "MONDO:0024711", "names": ["Malignant MEST", "malignant MEST", "Kidney Malignant Mixed Epithelial and Stromal Tumor", "Malignant Kidney Mixed Epithelial and Stromal Tumor", "Malignant Mixed Epithelial Stromal Tumor of the Kidney", "malignant mixed epithelial stromal tumor of the kidney", "mixed epithelial stromal tumor of the kidney, malignant", "Malignant Mixed Epithelial and Stromal Tumor of the Kidney"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant mixed epithelial stromal tumor of the kidney", "shortest_name_length": 14}
{"curie": "UMLS:C1333446", "names": ["Esophageal GIST", "Esophageal Gastrointestinal Stromal Tumor", "Esophageal Gastrointestinal Stromal Tumor (GIST)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Gastrointestinal Stromal Tumor", "shortest_name_length": 15}
{"curie": "MONDO:0001618", "names": ["Phallitis", "Balanoposthitis", "BALANOPOSTHITIS", "balanoposthitis", "Penis and sheath inflamed", "Balanoposthitis (disorder)", "Penis and prepuce inflamed", "balanoposthitis (diagnosis)", "Inflammation of penis and sheath", "Inflammation of penis and prepuce"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "balanoposthitis", "shortest_name_length": 9}
{"curie": "MONDO:0700019", "names": ["chromosome 12 disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 12 disorder", "shortest_name_length": 22}
{"curie": "MONDO:0021156", "names": ["Pituitary", "pituitary", "Hypophysis", "hypophysis", "Hypophysitis", "hypophysitis", "hypophysitides", "Hypophysitides", "Pituitary gland", "pituitary gland", "Pituitary Gland", "PITUITARY GLAND", "GLAND, PITUITARY", "gland, pituitary", "Hypophysis Cerebri", "hypophysis cerebri", "Hypophysitis (disorder)", "Nervous System, Pituitary", "nervous system, pituitary", "pituitary gland inflammation", "inflammation of pituitary gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypophysitis", "shortest_name_length": 9}
{"curie": "UMLS:C0852359", "names": ["Skin Ischemic Condition", "Skin ischemic conditions", "Skin ischaemic conditions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin ischaemic conditions", "shortest_name_length": 23}
{"curie": "UMLS:C0234474", "names": ["Graphomotor aphasia", "Graphomotor Aphasia", "Aphasia, graphomotor", "Aphasia, Graphomotor", "Graphomotor Aphasias", "Graphomotor aphasia (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aphasia, Graphomotor", "shortest_name_length": 19}
{"curie": "UMLS:C0280115", "names": ["stage II adult NHL", "NHL, stage II adult", "Stage II Non-Hodgkin Lymphoma", "Stage II Adult Non-Hodgkin Lymphoma", "stage II adult non-Hodgkin lymphoma", "Adult Non-Hodgkin's Lymphoma Stage II", "Stage II Adult Non-Hodgkin's Lymphoma", "non-Hodgkin's lymphoma, stage II adult", "adult non-Hodgkin's lymphoma, stage II", "lymphoma, stage II, adult non-Hodgkin's", "Ann Arbor Stage II Adult Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Adult Non-Hodgkin Lymphoma", "shortest_name_length": 18}
{"curie": "MONDO:0018209", "names": ["AxD type I", "Alexander disease type I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alexander disease type I", "shortest_name_length": 10}
{"curie": "UMLS:C1096660", "names": ["Ehlers-Danlos syndrome type IX"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ehlers-Danlos syndrome type IX", "shortest_name_length": 30}
{"curie": "UMLS:C0280158", "names": ["intermediate-grade, stage III adult NHL", "NHL, intermediate grade, stage III adult", "adult NHL, stage III, intermediate grade", "Stage III Intermediate Grade Adult Non-Hodgkin's Lymphoma", "adult non-Hodgkin's lymphoma, intermediate grade, stage III", "non-Hodgkin's lymphoma, intermediate grade, stage III adult", "lymphoma, intermediate grade, stage III adult non-Hodgkin's"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Intermediate Grade Adult Non-Hodgkin's Lymphoma", "shortest_name_length": 39}
{"curie": "MONDO:0003505", "names": ["femur cancer", "femoral cancer", "cancer of femur", "Femoral Neoplasm", "femoral neoplasm", "neoplasm of femur", "Neoplasm, Femoral", "Femoral Neoplasms", "Neoplasm of femur", "Neoplasms, Femoral", "cancer of the femur", "bone neoplasm of femur", "malignant femur neoplasm", "malignant neoplasm of femur", "Neoplasm of femur (disorder)", "neoplasm of femur (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "femoral cancer", "shortest_name_length": 12}
{"curie": "MONDO:0006745", "names": ["ess", "ESS", "Stromal sarcoma", "sarcoma stromal", "stromal sarcoma", "sarcoma endometrium", "Endometrial sarcoma", "endometrial sarcoma", "sarcoma; endometrial", "sarcoma, endometrial", "endometrium; sarcoma", "Stromal sarcoma, NOS", "ENDOMETRIUM, SARCOMA", "Sarcoma of endometrium", "Endometrial sarcoma, NOS", "Endometrial Stromal Sarcoma", "endometrial stromal sarcoma", "Endometrial stromal sarcoma", "stromal sarcoma, endometrial", "Sarcoma, Endometrial Stromal", "Endometrioid Stromal Sarcoma", "endometrial stromal sarcomas", "Endometrial Stromal Sarcomas", "Stromal Sarcoma, Endometrial", "endometrioid stromal sarcoma", "Sarcomas, Endometrial Stromal", "Stromal Sarcomas, Endometrial", "sarcomas, endometrial stromal", "stromal sarcomas, endometrial", "Undifferentiated uterine sarcoma", "Undifferentiated Uterine Sarcoma", "Sarcoma of endometrium (disorder)", "Sarcoma of endometrium (diagnosis)", "Stromal sarcoma of the corpus uteri", "stromal sarcoma of the corpus uteri", "UTERINE ENDOMETRIAL CANCER, SARCOMA", "Undifferentiated endometrial sarcoma", "undifferentiated endometrial sarcoma", "Endometrial stromal sarcoma (disorder)", "High grade endometrial stromal sarcoma", "Uterine Corpus Undifferentiated Sarcoma", "Endometrial stromal sarcoma, high grade", "STROMAL SARCOMA, ENDOMETRIAL, MALIGNANT", "stromal sarcoma, endometrial, malignant", "endometrial stromal sarcoma, high grade", "Endometrioid stromal sarcoma, high grade", "High grade endometrial stromal sarcoma (disorder)", "Uterine Corpus Undifferentiated Endometrial Sarcoma", "Endometrial stromal sarcoma (morphologic abnormality)", "Endometrial stromal sarcoma, high grade (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometrioid stromal sarcoma", "shortest_name_length": 3}
{"curie": "UMLS:C5420237", "names": ["Advanced GIST", "Advanced Gastrointestinal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Gastrointestinal Stromal Tumor", "shortest_name_length": 13}
{"curie": "MONDO:0043275", "names": ["TORCH syndrome", "TORCH Syndrome", "torch syndrome", "TORCH infection", "TORCH Infection", "TORCH SYNDROME CONGENITAL", "TORCH syndrome (diagnosis)", "Toxoplasma, rubella, cytomegalovirus AND herpes simplex mixed infection", "Toxoplasma, rubella, cytomegalovirus and herpes simplex mixed infection", "toxoplasmosis, other infections, rubella, cytomegalovirus, and herpes simplex virus syndrome", "Toxoplasmosis, other infections, rubella, cytomegalovirus, and herpes simplex virus syndrome", "toxoplasmosis, other infections, rubella, cytomegalovirus, and herpes simplex virus (torch) syndrome", "Toxoplasmosis, other infections, rubella, cytomegalovirus, and herpes simplex virus (TORCH) syndrome", "toxoplasmosis, Other infections, Rubella, Cytomegalovirus, and Herpes simplex Virus (TORCH) syndrome", "Toxoplasmosis, Other Infections, Rubella, Cytomegalovirus, and Herpes Simplex Virus (TORCH) Syndrome", "Toxoplasmosis, other infections, rubella, cytomegalovirus, and herpes simplex virus syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "TORCH syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0024182", "names": ["dry beriberi", "endemic neuritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dry beriberi", "shortest_name_length": 12}
{"curie": "MONDO:0021495", "names": ["benign sublingual gland tumor", "Benign Sublingual Gland Tumor", "benign sublingual gland neoplasm", "Benign Sublingual Gland Neoplasm", "sublingual gland benign neoplasm", "Benign tumor of sublingual gland", "Benign Tumor of Sublingual Gland", "benign tumor of sublingual gland", "Benign tumour of sublingual gland", "Benign Neoplasm of Sublingual Gland", "Benign neoplasm of sublingual gland", "benign neoplasm of sublingual gland", "benign tumor of the sublingual gland", "Benign Tumor of the Sublingual Gland", "benign neoplasm of the sublingual gland", "Benign Neoplasm of the Sublingual Gland", "Benign neoplasm of sublingual gland (disorder)", "benign neoplasm of sublingual gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of sublingual gland", "shortest_name_length": 29}
{"curie": "UMLS:C0278700", "names": ["Recurrent Liver Cancer", "Relapsed Pediatric Liver Cancer", "Relapsed Childhood Liver Cancer", "recurrent pediatric liver cancer", "recurrent childhood liver cancer", "Recurrent Pediatric Liver Cancer", "Recurrent Childhood Liver Cancer", "childhood liver cancer, recurrent", "pediatric liver cancer, recurrent", "Relapsed Childhood Cancer of Liver", "liver cancer, childhood, recurrent", "liver cancer, pediatric, recurrent", "Relapsed Pediatric Cancer of Liver", "Recurrent Pediatric Cancer of Liver", "Recurrent Childhood Cancer of Liver", "Relapsed Pediatric Cancer of the Liver", "Relapsed Childhood Cancer of the Liver", "Recurrent Childhood Cancer of the Liver", "Recurrent Pediatric Cancer of the Liver", "Recurrent Childhood Malignant Liver Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Liver Cancer", "shortest_name_length": 22}
{"curie": "UMLS:C4721578", "names": ["Stage IV Esophageal Cancer", "Stage IV Esophageal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Esophageal Cancer AJCC v7", "shortest_name_length": 26}
{"curie": "UMLS:C0854239", "names": ["Diverticulitis intestinal hemorrhagic", "Diverticulitis intestinal haemorrhagic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diverticulitis intestinal hemorrhagic", "shortest_name_length": 37}
{"curie": "UMLS:C5239038", "names": ["Myelodysplastic Syndrome, Unclassifiable, With 1 Percent Blasts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myelodysplastic Syndrome, Unclassifiable, With 1 Percent Blasts", "shortest_name_length": 63}
{"curie": "UMLS:C1261256", "names": ["Mycoplasma hominis pelvic inflammatory disease", "Pelvic inflammatory disease due to Mycoplasma hominis", "Pelvic inflammatory disease caused by Mycoplasma hominis", "Pelvic inflammatory disease due to Mycoplasma hominis (diagnosis)", "Pelvic inflammatory disease caused by Mycoplasma hominis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pelvic inflammatory disease due to Mycoplasma hominis", "shortest_name_length": 46}
{"curie": "UMLS:C1333063", "names": ["Classical Burkitt Lymphoma", "Classical Burkitt's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Classical Burkitt Lymphoma", "shortest_name_length": 26}
{"curie": "UMLS:C1336401", "names": ["Stage IVC Mouth Adenoid Cystic Carcinoma", "Stage IVC Adenoid Cystic Carcinoma of Mouth", "Stage IVC Oral Cavity Adenoid Cystic Cancer", "Stage IVC Oral Cavity Adenoid Cystic Carcinoma", "Stage IVC Adenoid Cystic Carcinoma of the Mouth", "Stage IVC Adenoid Cystic Carcinoma of Oral Cavity", "Stage IVC Adenoid Cystic Carcinoma of the Oral Cavity", "Stage IVC Oral Cavity Adenoid Cystic Carcinoma AJCC v7", "Stage IVC Oral Cavity Adenoid Cystic Carcinoma AJCC v6", "Stage IVC Oral Cavity Adenoid Cystic Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Oral Cavity Adenoid Cystic Carcinoma AJCC v6 and v7", "shortest_name_length": 40}
{"curie": "UMLS:C0393953", "names": ["Anterior Cerebral Circulation Infarction", "Anterior cerebral circulation infarction", "cerebral infarction anterior circulation", "Infarction, Anterior Cerebral Circulation", "Anterior cerebral circulation infarction (disorder)", "Anterior cerebral circulation infarction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anterior Cerebral Circulation Infarction", "shortest_name_length": 40}
{"curie": "UMLS:C4520975", "names": ["Pancreatic Cancer Stage IV", "Stage IV Pancreatic Cancer", "stage IV pancreatic cancer", "Stage IV Pancreatic Carcinoma", "Stage IV Carcinoma of Pancreas", "Stage IV Carcinoma of the Pancreas", "Stage IV Pancreatic Cancer AJCC v7", "Stage IV Pancreatic Cancer AJCC v6", "Stage IV Pancreatic Cancer AJCC v6 and v7", "Stage IV Exocrine and Endocrine Pancreatic Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Pancreatic Cancer AJCC v6 and v7", "shortest_name_length": 26}
{"curie": "UMLS:C0855193", "names": ["Testicular choriocarcinoma stage I", "Stage I Testicular Choriocarcinoma", "Stage I Testicular Choriocarcinoma AJCC v6", "Stage I Testicular Choriocarcinoma AJCC v7", "Stage I Testicular Choriocarcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular choriocarcinoma stage I", "shortest_name_length": 34}
{"curie": "UMLS:C1882198", "names": ["ORTI", "Ossifying renal tumor", "Ossifying Renal Tumor of Infancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ossifying Renal Tumor of Infancy", "shortest_name_length": 4}
{"curie": "UMLS:C4521881", "names": ["stage IB pleural mesothelioma", "stage IB malignant mesothelioma", "stage IB pleural mesothelioma AJCC v7", "Stage IB Pleural Malignant Mesothelioma", "Stage IB Pleural Malignant Mesothelioma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Pleural Malignant Mesothelioma AJCC v7", "shortest_name_length": 29}
{"curie": "UMLS:C1334228", "names": ["Intestinal GVHD", "Intestinal Graft Versus Host Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal Graft Versus Host Disease", "shortest_name_length": 15}
{"curie": "MONDO:0010102", "names": ["Taurodontia absent teeth sparse hair", "Taurodontia, Absent Teeth, And Sparse Hair", "TAURODONTIA, ABSENT TEETH, AND SPARSE HAIR", "taurodontia, absent teeth, and sparse hair", "taurodontia-absent teeth-sparse hair syndrome", "taurodontia, absent teeth, sparse hair syndrome", "teeth, congenital absence of, with taurodontia and sparse hair", "Teeth, congenital absence of, with taurodontia and sparse hair", "TEETH, CONGENITAL ABSENCE OF, WITH TAURODONTIA AND SPARSE HAIR"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "taurodontia-absent teeth-sparse hair syndrome", "shortest_name_length": 36}
{"curie": "MONDO:0014960", "names": ["PEBEL", "PEBEL1", "NAD(P)HX epimerase deficiency", "NAD(P)HX epimerase deficiency (disorder)", "Apolipoprotein A-I binding protein deficiency", "encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy", "ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY", "ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY, 1", "encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy; PEBEL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy", "shortest_name_length": 5}
{"curie": "MONDO:0010681", "names": ["myelolymphatic insufficiency", "Myelolymphatic insufficiency", "MYELOLYMPHATIC INSUFFICIENCY", "PELGER-LIKE ANOMALY WITH LEUKOPENIA AND SUSCEPTIBILITY TO INFECTIONS", "Pelger-like anomaly with leukopenia and susceptibility to infections"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myelolymphatic insufficiency", "shortest_name_length": 28}
{"curie": "MONDO:0000110", "names": ["bifid nose", "Bifid nose", "Cleft nose", "bifid; nose", "nose; bifid", "Bifid nasal bridge", "Cleft nasal bridge", "Nose, median cleft of", "Bifid nose (disorder)", "NOSE, MEDIAN CLEFT OF", "Median fissure of nose", "MEDIAN FISSURE OF NOSE", "Indented bridge of nose", "Indentation or clefting of the nose"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bifid nose", "shortest_name_length": 10}
{"curie": "UMLS:C5206854", "names": ["Metastatic Paranasal Sinus Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Paranasal Sinus Squamous Cell Carcinoma", "shortest_name_length": 50}
{"curie": "MONDO:0008070", "names": ["NEM3", "Nemaline Myopathy 3", "nemaline myopathy 3", "congenital myopathy 2A", "ACTA1 nemaline myopathy", "nemaline myopathy type 3", "Intranuclear Rod Myopathy", "Intranuclear Nemaline Rod Myopathy", "myopathy, actin, congenital, with cores", "Myopathy, Actin, Congenital, With Cores", "MYOPATHY, ACTIN, CONGENITAL, WITH CORES", "nemaline myopathy 3, with intranuclear rods", "NEMALINE MYOPATHY 3, WITH INTRANUCLEAR RODS", "Nemaline Myopathy 3, With Intranuclear Rods", "nemaline myopathy caused by mutation in ACTA1", "Nemaline Myopathy with Exclusively Intranuclear Rods", "nemaline myopathy 3, autosomal dominant or recessive", "MYOPATHY, ACTIN, CONGENITAL, WITH EXCESS OF THIN MYOFILAMENTS", "myopathy, actin, congenital, with Excess of thin myofilaments", "Myopathy, Actin, Congenital, with Excess of Thin Myofilaments"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nemaline myopathy 3", "shortest_name_length": 4}
{"curie": "UMLS:C1442835", "names": ["Solar rash", "Solar dermatitis", "solar dermatitis", "solar; dermatitis", "dermatitis; solar", "Dermatitis solaris", "dermatitis due to solar radiation", "dermatitis due to solar radiation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Solar dermatitis", "shortest_name_length": 10}
{"curie": "UMLS:C0542165", "names": ["Pseudoparkinsonism", "PSEUDOPARKINSONISM", "pseudoparkinsonism", "pseudoparkinsonism (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pseudoparkinsonism", "shortest_name_length": 18}
{"curie": "MONDO:0001853", "names": ["Contact blepharoconjunctivitis", "contact blepharoconjunctivitis", "Contact blepharoconjunctivitis (disorder)", "contact blepharoconjunctivitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "contact blepharoconjunctivitis", "shortest_name_length": 30}
{"curie": "MONDO:0020121", "names": ["MD", "Myodystrophy", "myodystrophy", "Myodystrophies", "Myodystrophica", "Myodystrophicas", "muscular dystrophy", "Dystrophy;muscular", "MUSCULAR DYSTROPHY", "Muscular Dystrophy", "Muscular dystrophy", "Dystrophy, Muscular", "muscular; dystrophy", "dystrophy; muscular", "muscular dystrophies", "Muscular Dystrophies", "Dystrophy (Muscular)", "Dystrophies, Muscular", "Muscular dystrophy NOS", "Muscular dystrophy, NOS", "MD - Muscular dystrophy", "Muscular dystrophy syndrome", "Muscular dystrophy (disorder)", "progressive muscular dystrophy", "Progressive muscular dystrophy", "PMD - Progressive muscular dystrophy", "Dystrophic muscle disease or syndrome", "Muscle biopsy shows dystrophic changes", "Dystrophic Muscle Diseases and Syndromes", "Hereditary progressive muscular dystrophy", "Congenital progressive muscular dystrophy", "hereditary progressive muscular dystrophy", "progressive muscular dystrophy (diagnosis)", "Progressive muscular dystrophy, hereditary", "muscular; dystrophy, hereditary (progressive)", "muscular; dystrophy, progressive (hereditary)", "dystrophy; muscular, progressive (hereditary)", "dystrophy; muscular, hereditary (progressive)", "Hereditary progressive muscular dystrophy, NOS", "Hereditary progressive muscular dystrophy (disorder)", "hereditary progressive muscular dystrophy (diagnosis)", "muscular; dystrophy, congenital (hereditary) (progressive)", "dystrophy; muscular, congenital (hereditary) (progressive)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy", "shortest_name_length": 2}
{"curie": "MONDO:0016295", "names": ["NCL", "ceroid lipofuscinosis", "ceroid-lipofuscinosis", "ceroid lipofuscinoses", "Ceroid Storage Disease", "Storage Disease, Ceroid", "Disease, Ceroid Storage", "Cerebral lipofuscinosis", "Ceroid Storage Diseases", "Cerebromacular dystrophy", "Lipofuscin Storage Disease", "Storage Disease, Lipofuscin", "Lipofuscin Storage Diseases", "Cerebromacular degeneration", "Disease, Lipofuscin Storage", "Neuronal Ceroid Lipofuscinosis", "Neuronal Ceroid Lipofuscinoses", "neuronal ceroid lipofuscinosis", "Neuronal Ceroid-Lipofuscinosis", "ceroid lipofuscinoses neuronal", "Neuronal ceroid-lipofuscinosis", "neuronal ceroid lipofuscinoses", "neuronal ceroid-lipofuscinosis", "Neuronal Ceroid-Lipofuscinoses", "Neuronal ceroid lipofuscinosis", "Lipofuscinosis, Neuronal Ceroid", "Ceroid Lipofuscinosis, Neuronal", "Ceroid-Lipofuscinosis, Neuronal", "hereditary ceroid lipofuscinosis", "Neuronal ceroid lipofuscinosis NOS", "Cerebroretinal degeneration disease", "neuronal ceroid lipofuscinosis (CLN)", "Neuronal ceroid lipofuscinosis (disorder)", "neuronal ceroid lipofuscinosis (diagnosis)", "Pigmentary retinal lipoid neuronal heredodegeneration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuronal ceroid lipofuscinosis", "shortest_name_length": 3}
{"curie": "UMLS:C4520734", "names": ["Stage 0 Sinonasal Cancer AJCC v6, v7, and v8", "Stage 0 Nasal Cavity and Paranasal Sinus Cancer", "Stage 0 Sinonasal Carcinoma AJCC v6, v7, and v8", "Stage 0 Nasal Cavity and Paranasal Sinus Cancer AJCC v7", "Stage 0 Nasal Cavity and Paranasal Sinus Cancer AJCC v6", "Stage 0 Nasal Cavity and Paranasal Sinus Cancer AJCC v8", "stage 0 nasal cavity and ethmoid sinus carcinoma in situ", "Stage 0 Nasal Cavity and Paranasal Sinus Carcinoma AJCC v8", "Stage 0 Nasal Cavity and Paranasal Sinus Cancer AJCC v6, v7, and v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Sinonasal Cancer AJCC v6, v7, and v8", "shortest_name_length": 44}
{"curie": "UMLS:C0438413", "names": ["Malignant neoplasm of aortic body and other paraganglia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant neoplasm of aortic body and other paraganglia", "shortest_name_length": 55}
{"curie": "MONDO:0009676", "names": ["LGMD3", "LGMDR2", "LGMD2B", "LGMD type 2B", "LGMD R2 dysferlin-related", "Dysferlin-related LGMD R2", "LGMD due to dysferlin deficiency", "limb-girdle muscular dystrophy type 3", "Limb girdle muscular dystrophy type 2B", "Limb-girdle muscular dystrophy type 2B", "Limb-Girdle Muscular Dystrophy Type 2B", "limb-girdle muscular dystrophy type 2B", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 3", "muscular dystrophy, limb-girdle, type 3", "limb-girdle muscular dystrophy, type 2B", "Muscular dystrophy, limb-girdle, type 3", "Limb-girdle muscular dystrophy, type 2B", "muscular dystrophy, limb-girdle, type 2B", "Muscular Dystrophy, Limb-Girdle, Type 2B", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B", "Dysferlin-related limb-girdle muscular dystrophy R2", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 2", "muscular dystrophy, limb-girdle, autosomal recessive 2", "DYSF autosomal recessive limb-girdle muscular dystrophy", "autosomal recessive limb-girdle muscular dystrophy type 2B", "Autosomal recessive limb girdle muscular dystrophy type 2B", "limb-girdle muscular dystrophy due to dysferlin deficiency", "Autosomal recessive limb-girdle muscular dystrophy type 2B", "Limb girdle muscular dystrophy due to dysferlin deficiency", "Limb-girdle muscular dystrophy due to dysferlin deficiency", "Autosomal recessive limb girdle muscular dystrophy type 2B (disorder)", "autosomal recessive limb-girdle muscular dystrophy caused by mutation in DYSF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive limb-girdle muscular dystrophy type 2B", "shortest_name_length": 5}
{"curie": "UMLS:C0031557", "names": ["PHLEGMON", "Phlegmon", "phlegmon", "Phlegmonous cellulitis", "Phlegmon (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Phlegmon", "shortest_name_length": 8}
{"curie": "UMLS:C2981405", "names": ["Stage IVB Colorectal Cancer", "Stage IVB Colorectal Cancer AJCC v7", "Stage IVB Colorectal (Colon or Rectal) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Colorectal Cancer AJCC v7", "shortest_name_length": 27}
{"curie": "MONDO:0016386", "names": ["Chang Davidson Carlson syndrome", "Chang-Davidson-Carlson syndrome", "Hypogonadotropic hypogonadism-retinitis pigmentosa syndrome", "hypogonadotropic hypogonadism-retinitis pigmentosa syndrome", "Hypogonadotropic hypogonadism retinitis pigmentosa syndrome", "Hypogonadotropic hypogonadism retinitis pigmentosa syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadotropic hypogonadism-retinitis pigmentosa syndrome", "shortest_name_length": 31}
{"curie": "UMLS:C4727168", "names": ["Advanced Unresectable Gastric Adenocarcinoma", "Unresectable Advanced Gastric (Stomach) Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Unresectable Gastric Adenocarcinoma", "shortest_name_length": 44}
{"curie": "MONDO:0013018", "names": ["KFSD", "autosomal dominant keratosis follicularis spinulosa decalvans", "Keratosis Follicularis Spinulosa Decalvans, Autosomal Dominant", "keratosis follicularis SPINULOSA decalvans, autosomal dominant", "keratosis follicularis spinulosa decalvans, autosomal dominant", "KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT", "KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratosis follicularis spinulosa decalvans, autosomal dominant", "shortest_name_length": 4}
{"curie": "MONDO:0010451", "names": ["MRX41", "MRX48", "XLID41", "X-linked mental retardation 48", "X-linked mental retardation 41", "MENTAL RETARDATION, X-LINKED 48", "MENTAL RETARDATION, X-LINKED 41", "mental retardation, X-linked 48", "mental retardation, X-linked 41", "intellectual disability, X-linked 41", "intellectual disability, X-linked 48", "mental retardation, X-linked type 41", "intellectual disability, X-linked type 41", "X-linked mental retardation 41 (MRX41, XLMR41)", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 41", "non-syndromic X-linked intellectual disability 41", "GDI1 non-syndromic X-linked intellectual disability", "intellectual developmental disorder, X-linked 41, X-linked dominant", "non-syndromic X-linked intellectual disability caused by mutation in GDI1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 41", "shortest_name_length": 5}
{"curie": "MONDO:0013237", "names": ["MNMN", "MONONEUROPATHY OF THE MEDIAN NERVE, MILD", "mononeuropathy of the median nerve, mild", "CARPAL TUNNEL SYNDROME, SUSCEPTIBILITY TO", "carpal tunnel syndrome, susceptibility to", "susceptibility to mononeuropathy of the median nerve, mild"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "susceptibility to mononeuropathy of the median nerve, mild", "shortest_name_length": 4}
{"curie": "MONDO:0017265", "names": ["ARCI", "lamellar ichthyosis", "autosomal recessive inherited ichthyosis", "inherited ichthyosis, autosomal recessive", "autosomal recessive congenital ichthyosis", "ichthyosis, congenital, autosomal recessive", "non bullous congenital ichthyosiform erythroderma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive congenital ichthyosis", "shortest_name_length": 4}
{"curie": "MONDO:0014061", "names": ["STLS", "STEEL SYNDROME", "steel syndrome", "Steel syndrome", "DISLOCATED HIPS AND RADIAL HEADS, CARPAL COALITION, SCOLIOSIS, AND SHORT STATURE", "dislocated hips and radial heads, carpal coalition, scoliosis, and short stature", "bilateral hip and radial head dislocations-short stature-scoliosis-carpal coalitions-pes cavus-facial dysmorphism syndrome", "Bilateral hip and radial head dislocations-short stature-scoliosis-carpal coalitions-pes cavus-facial dysmorphism syndrome", "Bilateral hip and radial head dislocations, short stature, scoliosis, carpal coalition, pes cavus, facial dysmorphism syndrome", "Bilateral hip and radial head dislocations, short stature, scoliosis, carpal coalition, pes cavus, facial dysmorphism syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Steel syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0014846", "names": ["SCAR23", "autosomal recessive spinocerebellar ataxia 23", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 23", "spinocerebellar ataxia, autosomal recessive 23", "Spinocerebellar ataxia autosomal recessive type 23", "spinocerebellar ataxia autosomal recessive type 23", "spinocerebellar ataxia, autosomal recessive type 23", "SCAR23 - spinocerebellar ataxia autosomal recessive type 23", "autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to TUD deficiency", "Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to TUD deficiency", "Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency", "autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome due to TUD deficiency", "Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency (disorder)", "Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome due to TUD deficiency", "shortest_name_length": 6}
{"curie": "MONDO:0015902", "names": ["major hypertriglyceridemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "major hypertriglyceridemia", "shortest_name_length": 26}
{"curie": "MONDO:0006091", "names": ["Appendix NET G1", "appendix NET G1", "carcinoid appendix", "appendix carcinoid", "appendix; carcinoid", "appendix carcinoids", "carcinoid; appendix", "Carcinoid of appendix", "carcinoid of appendix", "Carcinoid, of appendix", "carcinoid tumor appendix", "appendix carcinoid tumor", "Appendix Carcinoid Tumor", "Appendix carcinoid tumor", "vermiform appendix NET G1", "Appendix carcinoid tumour", "appendix carcinoid tumors", "Carcinoid tumor of appendix", "carcinoid tumor of appendix", "Appendix NET G1 (Carcinoid)", "Carcinoid, NOS, of appendix", "appendix NET G1 (carcinoid)", "Carcinoid Tumor of Appendix", "Appendiceal Carcinoid Tumor", "appendiceal carcinoid tumor", "Carcinoid tumor, argentaffin", "Carcinoid tumor, of appendix", "Carcinoid tumour of appendix", "Carcinoid tumour, of appendix", "Carcinoid tumour, argentaffin", "carcinoid tumor of the appendix", "Carcinoid Tumor of the Appendix", "Carcinoid tumor of the appendix", "Appendix Neuroendocrine Tumor G1", "appendix neuroendocrine tumor G1", "Carcinoid tumour of the appendix", "Carcinoid tumor NOS, of appendix", "Carcinoid tumour NOS, of appendix", "Carcinoid tumor, NOS, of appendix", "Carcinoid tumour, NOS, of appendix", "vermiform appendix carcinoid tumor", "appendix carcinoid endocrine tumour", "Carcinoid tumor of appendix (disorder)", "vermiform appendix carcinoid tumor (disease)", "Appendix Neuroendocrine Tumor G1 (Carcinoid)", "appendix neuroendocrine tumor G1 (carcinoid)", "vermiform appendix neuroendocrine neoplasm G1", "Carcinoid tumor of uncertain malignant potential", "Carcinoid tumour of uncertain malignant potential", "grade 1 neuroendocrine neoplasm of vermiform appendix", "vermiform appendix neuroendocrine tumor, well differentiated, low grade", "Carcinoid tumor of uncertain malignant potential (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "appendix neuroendocrine tumor G1", "shortest_name_length": 15}
{"curie": "UMLS:C0009354", "names": ["Closed Colles' Fracture", "Closed Colles' fracture", "Fracture, closed, Colles'", "Fracture, closed, colles'", "closed Colles' fracture of wrist", "Closed Colles' fracture (disorder)", "closed Colles' fracture of wrist (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Closed Colles' fracture", "shortest_name_length": 23}
{"curie": "UMLS:C1336084", "names": ["bronchial dysplasia", "Lung Squamous Dysplasia", "squamous lung dysplasia", "Squamous Lung Dysplasia", "Bronchial Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Squamous Lung Dysplasia", "shortest_name_length": 19}
{"curie": "MONDO:0100437", "names": ["RP3", "COD1", "CORDX1", "RPGR retinopathy", "retinitis pigmentosa 3", "retinitis pigmentosa 15", "RPGR-related retinopathy", "cone dystrophy X-linked 1", "X-linked cone dystrophy 1", "RPGR retinitis pigmentosa", "cone dystrophy 1, X-linked", "retinitis pigmentosa type 3", "X-linked cone-rod dystrophy 1", "cone-rod dystrophy X-linked 1", "cone-rod dystrophy, X-linked, 1", "cone-rod degeneration, X-linked", "X-linked cone-rod dystrophy type 1", "cone-rod dystrophy, X-linked, type 1", "macular degeneration, X-linked atrophic", "retinitis pigmentosa caused by mutation in RPGR", "retinal ciliopathy due to mutation in the RPGR gene", "choroidoretinal degeneration with retinal reflex in heterozygous women"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "RPGR-related retinopathy", "shortest_name_length": 3}
{"curie": "MONDO:0012833", "names": ["CAN", "can", "chronic allograft nephropathy", "Chronic Allograft Nephropathy", "Chronic allograft nephropathy", "Chronic transplant nephropathy", "CROUZONODERMOSKELETAL SYNDROME", "Crouzonodermoskeletal Syndrome", "Crouzonodermoskeletal syndrome", "Crouzon-dermoskeletal syndrome", "Chronic kidney allograft nephropathy", "Chronic Kidney Allograft Nephropathy", "Chronic rejection of renal transplant", "Crouzon Syndrome With Acanthosis Nigricans", "Crouzon syndrome with acanthosis nigricans", "CROUZON SYNDROME WITH ACANTHOSIS NIGRICANS", "Crouzon syndrome-acanthosis nigricans syndrome", "complication renal transplant rejection chronic", "Chronic rejection of renal transplant (disorder)", "Chronic rejection of renal transplant (diagnosis)", "CROUZON SYNDROME WITH ACANTHOSIS NIGRICANS (disorder)", "Crouzon syndrome with acanthosis nigricans (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Crouzon syndrome-acanthosis nigricans syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0023221", "names": ["Gaucher ichthyosis restrictive dermopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gaucher ichthyosis restrictive dermopathy", "shortest_name_length": 41}
{"curie": "UMLS:C4683431", "names": ["Stage II Thyroid Gland Follicular Cancer 55 Years and Older", "Stage II Thyroid Gland Follicular Carcinoma 55 Years and Older AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Thyroid Gland Follicular Carcinoma 55 Years and Older AJCC v8", "shortest_name_length": 59}
{"curie": "NCIT:C27268", "names": ["Lymphoma by Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoma by Stage", "shortest_name_length": 17}
{"curie": "UMLS:C5670551", "names": ["Metastatic Primary Peritoneal High-Grade Serous Adenocarcinoma", "Metastatic Primary Peritoneal High Grade Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Primary Peritoneal High Grade Serous Adenocarcinoma", "shortest_name_length": 62}
{"curie": "MONDO:0023137", "names": ["feigenbaum Bergeron syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "feigenbaum Bergeron syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0015525", "names": ["Congenital pseudarthrosis", "congenital pseudoarthrosis", "Congenital pseudoarthrosis", "congenital pseudarthrosis of the limbs", "congenital pseudoarthrosis of the limbs", "Congenital pseudoarthrosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital pseudoarthrosis of the limbs", "shortest_name_length": 25}
{"curie": "MONDO:0024557", "names": ["Atld", "ATLD", "ATLD1", "Ataxia-Telangiectasia-Like Disorder", "Ataxia Telangiectasia Like Disorder", "ataxia-telangiectasia-like disorder", "Ataxia-telangiectasia-like disorder", "ATAXIA-TELANGIECTASIA-LIKE DISORDER", "Ataxia-Telangiectasia-Like Disorder 1", "ataxia-telangiectasia-like disorder 1", "ATAXIA-TELANGIECTASIA-LIKE DISORDER 1", "Ataxia-Telangiectasisa-Like Disorder 1", "MRE11 ataxia-telangiectasia-like disorder", "MRE11 ataxia - telangiectasia-like disorder", "Ataxia-telangiectasia-like disorder (disorder)", "ataxia-telangiectasia-like disorder (diagnosis)", "ataxia-telangiectasia-like disorder caused by mutation in MRE11", "ataxia - telangiectasia-like disorder caused by mutation in MRE11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ataxia-telangiectasia-like disorder 1", "shortest_name_length": 4}
{"curie": "UMLS:C1335257", "names": ["Stage 3 Hepatoblastoma", "PRETEXT Stage 3 Hepatoblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PRETEXT Stage 3 Hepatoblastoma", "shortest_name_length": 22}
{"curie": "MONDO:0009387", "names": ["HDLCQ11", "Bürger-Grütz", "LPL deficiency", "LPL DEFICIENCY", "lipd deficiency", "LIPD Deficiency", "LIPD DEFICIENCY", "Deficiency, LIPD", "LIPD Deficiencies", "Deficiencies, LIPD", "lipase D deficiency", "LIPASE D DEFICIENCY", "Lipase D Deficiency", "Hyperchylomicronemia", "Deficiency, Lipase D", "hyperchylomicronemia", "Burger-Grutz Syndrome", "Lipase D Deficiencies", "Hyperchylomicronaemia", "burger-grutz syndrome", "Burger-Grutz syndrome", "Burger Grutz syndrome", "Burger Grutz Syndrome", "Burger-Grutz Syndromes", "Syndrome, Burger-Grutz", "Deficiencies, Lipase D", "Familial LPL Deficiency", "BUERGER-GRUETZ SYNDROME", "Hyperlipidemia, Group D", "hyperlipidemia; group D", "HYPERLIPEMIA, RETENTION", "familial LPL deficiency", "Hyperlipidemia, group D", "Mixed hyperglyceridemia", "Syndromes, Burger-Grutz", "mixed hyperglyceridemia", "Familial LPL deficiency", "hyperglyceridemia; mixed", "Familial Chylomicronemia", "LPL Deficiency, Familial", "Deficiency, Familial LPL", "mixed; hyperglyceridemia", "Familial Chylomicronemias", "Chylomicronemia, Familial", "CHYLOMICRONEMIA, FAMILIAL", "chylomicronemia, familial", "Familial LPL Deficiencies", "Chylomicronemias, Familial", "Deficiencies, Familial LPL", "LPL Deficiencies, Familial", "type I hyperlipoproteinemia", "Type I hyperlipoproteinemia", "HYPERLIPOPROTEINEMIA TYPE I", "Fredrickson type I lipaemia", "Hyperlipoproteinemia Type I", "Type I Hyperlipoproteinemia", "hyperlipoproteinemia type I", "type i hyperlipoproteinemia", "hyperlipoproteinemia type i", "Hyperlipoproteinemia Type Ia", "Hyperlipoproteinemia, Type I", "Hyperlipoproteinemia Type Is", "Type I hyperlipoproteinaemia", "Primary hyperchylomicronemia", "Hyperlipoproteinemia, type I", "hyperlipoproteinemia, type I", "Type Ia Hyperlipoproteinemia", "Type I Hyperlipoproteinemias", "HYPERLIPOPROTEINEMIA, TYPE I", "Hyperlipoproteinemia Type 1A", "hyperlipoproteinemia, type 1", "Hyperlipoproteinemias, Type I", "LIPOPROTEIN LIPASE DEFICIENCY", "Hyperlipoproteinemia Type Ias", "lipoprotein lipase deficiency", "FAMILIAL HYPERCHYLOMICRONEMIA", "Lipoprotein-lipase deficiency", "HYPERLIPOPROTEINEMIA, TYPE IA", "Familial hyperchylomicronemia", "Familial Hyperchylomicronemia", "hyperlipoproteinemia, type 1A", "Type Ia Hyperlipoproteinemias", "Lipoprotein Lipase Deficiency", "Primary hyperchylomicronaemia", "Hyperlipoproteinemia, Type Ia", "familial hyperchylomicronemia", "Hyperlipoproteinaemia, type I", "Deficiency, Lipoprotein Lipase", "Hyperlipoproteinemias, Type Ia", "Hyperchylomicronemia, Familial", "hyperchylomicronemia, familial", "Familial hyperchylomicronaemia", "HYPERCHYLOMICRONEMIA, FAMILIAL", "Hepatosplenomegalic lipoidosis", "Familial Hyperchylomicronemias", "Endogenous hypertriglyceridemia", "Hyperchylomicronemias, Familial", "ENDOGENOUS HYPERTRIGLYCERIDEMIA", "Familial Essential Hyperlipemia", "Essential Familial Hyperlipemia", "endogenous hypertriglyceridemia", "Lipoprotein Lipase Deficiencies", "Lipase Deficiencies, Lipoprotein", "Hyperlipemia, Essential Familial", "HYPERLIPEMIA, ESSENTIAL FAMILIAL", "hyperlipemia, essential familial", "Endogenous hypertriglyceridaemia", "Deficiencies, Lipoprotein Lipase", "endogenous hypertriglyceridaemia", "familial chylomiconemia syndrome", "Familial Hyperlipemia, Essential", "hyperchylomicronemia (diagnosis)", "Essential Familial Hyperlipemias", "Hyperlipemias, Essential Familial", "Familial Hyperlipemias, Essential", "familial chylomicronemia syndrome", "Fredrickson type I hyperlipidemia", "HYPERLIPEMIA, IDIOPATHIC FAMILIAL", "Hypercholesterinemic xanthomatosis", "hypercholesterinaemic xanthomatosis", "Hypercholesterinaemic xanthomatosis", "Familial type I hyperlipoproteinemia", "Familial Hyperlipoproteinemia Type 1", "familial hyperlipoproteinemia type I", "Familial hyperlipoproteinemia, type I", "Familial type I hyperlipoproteinaemia", "Familial lipoprotein lipase deficiency", "Familial hyperlipoproteinaemia, type I", "Familial Lipoprotein Lipase Deficiency", "familial lipoprotein lipase deficiency", "hyperlipoproteinemia type I (diagnosis)", "Fredrickson type I hyperlipoproteinemia", "Fredrickson type 1 hyperlipoproteinemia", "Lipoprotein Lipase Deficiency, Familial", "lipoprotein lipase deficiency, familial", "Fredrickson type 1 hyperlipoproteinaemia", "hyperlipoproteinemia; Fredrickson type I", "Fredrickson type I hyperlipoproteinaemia", "Fredrickson; type I hyperlipoproteinemia", "Familial hyperchylomicronemia (disorder)", "Familial fat-induced hypertriglyceridemia", "familial fat-induced hypertriglyceridemia", "Hyperlipoproteinemia, Frederickson type I", "Familial fat-induced hypertriglyceridaemia", "Hyperlipemia, Idiopathic, Burger-Grutz Type", "hyperlipemia, idiopathic, Burger-Grutz type", "HYPERLIPEMIA, IDIOPATHIC, BURGER-GRUTZ TYPE", "Fredrickson type I or V hyperlipoproteinemia", "Fredrickson type I hyperlipidemia (diagnosis)", "Fredrickson's hyperlipoproteinemia, type I or V", "Familial lipoprotein lipase deficiency (disorder)", "high density lipoprotein cholesterol level QTL 11", "familial lipoprotein lipase deficiency (diagnosis)", "Familial lipoprotein lipase deficiency with type I phenotype", "familial lipoprotein lipase deficiency with type I phenotype", "familial lipoprotein lipase deficiency (disorder) [ambiguous]", "HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 11", "Familial lipoprotein lipase deficiency with type I phenotype (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial lipoprotein lipase deficiency", "shortest_name_length": 7}
{"curie": "MONDO:0009285", "names": ["GTG deficiency", "Glutathionuria", "GTG DEFICIENCY", "GGT deficiency", "GGT DEFICIENCY", "glutathionuria", "GLUTATHIONURIA", "GGT1 deficiency", "Glutathioninuria", "glutathioninuria", "GAMMA-GLUTAMYLTRANSFERASE DEFICIENCY", "gamma-Glutamyltransferase deficiency", "gamma-glutamyltransferase deficiency", "Gamma-glutamyltransferase deficiency", "gamma-glutamyl transferase deficiency", "Gamma-glutamyl transferase deficiency", "GAMMA-GLUTAMYLTRANSPEPTIDASE DEFICIENCY", "gamma-glutamyltranspeptidase deficiency", "Gamma-glutamyltranspeptidase deficiency", "Gamma-glutamyl transpeptidase deficiency", "gamma-glutamyl transpeptidase deficiency", "gamma-Glutamyl transpeptidase deficiency", "inborn error of glutathione hydrolase activity", "inborn glutathione hydrolase activity disorder", "rare inborn error of glutathione hydrolase activity", "Gamma-glutamyl transpeptidase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gamma-glutamyl transpeptidase deficiency", "shortest_name_length": 14}
{"curie": "MONDO:0004812", "names": ["Acute dacryoadenitis", "acute dacryoadenitis", "dacryoadenitis, acute", "DACRYOADENITIS, ACUTE", "Acute dacryoadenitis (disorder)", "acute dacryoadenitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute dacryoadenitis", "shortest_name_length": 20}
{"curie": "MONDO:0013578", "names": ["MRD7", "DYRK1A syndrome", "autosomal dominant mental retardation 7", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 7", "mental retardation, autosomal dominant 7", "Mental Retardation, Autosomal Dominant 7", "autosomal dominant intellectual disability 7", "mental retardation, autosomal dominant type 7", "intellectual disability, autosomal dominant 7", "DYRK1A-related intellectual disability syndrome", "intellectual disability, autosomal dominant type 7", "autosomal dominant intellectual developmental disorder 7", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7", "autosomal dominant non-syndromic intellectual disability 7", "Dual specificity tyrosine phosphorylation regulated kinase 1A-related intellectual disability syndrome", "DYRK1A (dual specificity tyrosine phosphorylation regulated kinase 1A)-related intellectual disability syndrome", "Dual specificity tyrosine phosphorylation regulated kinase 1A-related intellectual disability syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DYRK1A-related intellectual disability syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0007067", "names": ["pyruvate kinase hyperactivity", "Pyruvate Kinase Hyperactivity", "PYRUVATE KINASE HYPERACTIVITY", "Pyruvate kinase hyperactivity", "Adenosine Triphosphate, Elevated, Of Erythrocytes", "ADENOSINE TRIPHOSPHATE, ELEVATED, OF ERYTHROCYTES", "adenosine triphosphate, elevated, of erythrocytes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyruvate kinase hyperactivity", "shortest_name_length": 29}
{"curie": "MONDO:0021105", "names": ["FLD1", "NAFLD1", "FATTY LIVER DISEASE, SUSCEPTIBILITY TO, 1", "liver disease, alcoholic, susceptibility to, 1", "LIVER DISEASE, ALCOHOLIC, SUSCEPTIBILITY TO, 1", "FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 1", "fatty liver disease, nonalcoholic, susceptibility to, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "NAFLD1", "shortest_name_length": 4}
{"curie": "MONDO:0018202", "names": ["gonadal germ cell tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gonadal germ cell tumor", "shortest_name_length": 23}
{"curie": "MONDO:0003917", "names": ["PCL", "Heart Lymphoma", "heart lymphoma", "Cardiac Lymphoma", "Cardiac lymphoma", "Lymphoma of heart", "Lymphoma of Heart", "lymphoma of heart", "lymphoma of the heart", "Lymphoma of the Heart", "Primary Heart Lymphoma", "Primary heart lymphoma", "primary Cardiac lymphoma", "Primary Cardiac Lymphoma", "Lymphoma of heart (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heart lymphoma", "shortest_name_length": 3}
{"curie": "MONDO:0001132", "names": ["Sadism", "sadism", "Sadisms", "Sadism, NOS", "Sexual sadism", "Sexual Sadism", "sexual sadism", "Sadism, Sexual", "Sexual Sadisms", "Sadisms, Sexual", "Sadism (finding)", "Sadistic torture", "sadistic behavior", "Sadistic behavior", "sadistic behaviour", "Sadistic behaviour", "Sexual sadism disorder", "sexual sadism disorder", "Sexual sadism (disorder)", "Sadistic torture (finding)", "sadistic behavior (symptom)", "sexual sadism disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sexual sadism disorder", "shortest_name_length": 6}
{"curie": "MONDO:0019879", "names": ["trisomy 4qter", "Trisomy 4qter", "distal trisomy 4q", "Distal trisomy 4q", "Distal duplication 4q", "distal duplication 4q", "distal trisomy type 4q", "Telomeric duplication 4q", "telomeric duplication 4q", "Distal trisomy 4q (disorder)", "Distal trisomy 4q (diagnosis)", "anomaly of chromosome pair distal trisomy 4q"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal trisomy 4q", "shortest_name_length": 13}
{"curie": "MONDO:0024608", "names": ["DIENTAMEBIASIS", "Dientamebiasis", "Dientamoebiases", "dientamoebiasis", "Dientamoebiasis", "Trichomoniasis intestinal", "Intestinal trichomoniasis", "intestinal trichomoniasis", "trichomoniasis; intestinal", "Trichomoniasis, intestinal", "intestinal; trichomoniasis", "Trichomonas hominis infection", "Dientamoeba infectious disease", "Dientamoeba disease or disorder", "Intestinal infection by Trichomonas", "Intestinal trichomoniasis (disorder)", "intestinal trichomoniasis (diagnosis)", "Dientamoeba caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dientamoebiasis", "shortest_name_length": 14}
{"curie": "MONDO:0012352", "names": ["vasculitis, lymphocytic, cutaneous small vessel", "VASCULITIS, LYMPHOCYTIC, CUTANEOUS SMALL VESSEL", "Vasculitis, Lymphocytic, Cutaneous Small Vessel"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vasculitis, lymphocytic, cutaneous small vessel", "shortest_name_length": 47}
{"curie": "OMIM:111380", "names": [], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"]}
{"curie": "MONDO:0013319", "names": ["CHROMOSOME 4q32.1-q32.2 TRIPLICATION SYNDROME", "chromosome 4Q32.1-q32.2 triplication syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 4Q32.1-q32.2 triplication syndrome", "shortest_name_length": 45}
{"curie": "MONDO:0008579", "names": ["TOES, RELATIVE LENGTH OF FIRST AND SECOND", "toes, relative length of first and second"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "toes, relative length of first and second", "shortest_name_length": 41}
{"curie": "MONDO:0004902", "names": ["keratitis interstitial", "Keratitis interstitial", "Interstitial keratitis", "interstitial keratitis", "KERATITIS INTERSTITIAL", "interstitial; keratitis", "keratitis; interstitial", "IK - Interstitial keratitis", "Interstitial keratitis, NOS", "Interstitial keratitis (disorder)", "Unspecified interstitial keratitis", "interstitial keratitis (diagnosis)", "Interstitial keratitis, unspecified", "interstitial keratitis was observed", "interstitial keratitis (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "interstitial keratitis", "shortest_name_length": 22}
{"curie": "MONDO:0033671", "names": ["SPGF45", "SPERMATOGENIC FAILURE 45", "spermatogenic failure 45"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 45", "shortest_name_length": 6}
{"curie": "UMLS:C5237728", "names": ["Recurrent Myeloproliferative Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Myeloproliferative Neoplasm", "shortest_name_length": 37}
{"curie": "UMLS:C0280364", "names": ["Recurrent Lip Basal Cell Cancer", "Relapsed Lip Basal Cell Carcinoma", "Recurrent Lip Basal Cell Carcinoma", "lip basal cell carcinoma, recurrent", "Relapsed Basal Cell Carcinoma of Lip", "Recurrent Basal Cell Carcinoma of Lip", "Relapsed Basal Cell Carcinoma of the Lip", "Recurrent Basal Cell Carcinoma of the Lip", "recurrent basal cell carcinoma of the lip", "basal cell carcinoma of the lip, recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Lip Basal Cell Carcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C4520991", "names": ["Stage II Liver Cell Cancer", "Liver Cell Cancer Stage II", "Stage II Liver Cell Carcinoma", "Stage II Hepatocellular Cancer", "Hepatocullular Cancer Stage II", "Stage II Hepatocellular Carcinoma AJCC v6", "Stage II Hepatocellular Carcinoma AJCC v7", "Stage II Hepatocellular Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Hepatocellular Carcinoma AJCC v6 and v7", "shortest_name_length": 26}
{"curie": "UMLS:C0525046", "names": ["Schizophrenia and Disorders with Psychotic Features", "Schizophrenia Spectrum and Other Psychotic Disorders", "Schizophrenia spectrum and other psychotic disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Schizophrenia Spectrum and Other Psychotic Disorders", "shortest_name_length": 51}
{"curie": "UMLS:C4683576", "names": ["Lugano Classification Stage I Adult Non-Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage I Adult Non-Hodgkin Lymphoma AJCC v8", "shortest_name_length": 64}
{"curie": "MONDO:0016608", "names": ["Large head", "Large skull", "Megacephaly", "Macrocrania", "Macrocephaly", "MACROCEPHALY", "macrocephaly", "Macrocephalus", "macrocephalus", "Megacephalies", "megalocephaly", "Macrencephaly", "Megalocephaly", "macrencephaly", "Macrocephalies", "Macroencephaly", "macroencephaly", "megalencephaly", "Enlarged brain", "Megalencephaly", "Megalocephalies", "Megalencephalies", "Macrocephaly NOS", "Skull enlargement", "Large head (disorder)", "Isolated macrencephaly", "Isolated megalencephaly", "megalencephaly (disease)", "macrocephaly (diagnosis)", "Macroencephaly (disorder)", "macroencephaly (diagnosis)", "megalencephaly (diagnosis)", "congenital deformity of head macrocephaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "megalencephaly", "shortest_name_length": 10}
{"curie": "MONDO:0001836", "names": ["amenia", "amenorrhea", "Amenorrhea", "AMENORRHEA", "Amenorrhoea", "amenorrhoea", "AMENORRHOEA", "Amenorrhea NOS", "Menses lack of", "lack of menses", "MENSES LACK OF", "Amenorrhea, NOS", "Amenorrhoea NOS", "Amenorrhoea, NOS", "cessation of menses", "CESSATION OF MENSES", "menstruation absence", "Amenorrhea (finding)", "amenorrhea (disease)", "absence; menstruation", "amenorrhea (diagnosis)", "absence of menstruation", "Absence of menstruation", "Amenorrhea, unspecified", "Amenorrhoea, unspecified", "Absence of menstruation, NOS", "Abnormal absence of menstruation", "menstrual periods stopped for over 6 months", "menstrual periods stopped for over 6 months (symptom)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amenorrhea", "shortest_name_length": 6}
{"curie": "MONDO:0021068", "names": ["ovary tumor", "ovary cancer", "ovary tumors", "ovary; tumor", "ovary tumour", "Ovarian tumor", "ovarian tumor", "Ovarian Tumor", "Ovarian tumour", "Ovarian Tumors", "Ovarian cancer", "ovarian tumors", "Tumor of ovary", "ovarian tumour", "ovary neoplasm", "Ovary Neoplasm", "Tumor of Ovary", "ovarian cancer", "tumor of ovary", "Ovary Neoplasms", "Tumour of ovary", "Ovaries--Tumors", "Neoplasm, Ovary", "ovarian tumours", "ovary neoplasms", "ovarian neoplasm", "Ovarian Neoplasm", "Neoplasms, Ovary", "Ovarian neoplasm", "ovarian neoplasms", "neoplasm of ovary", "OVARIAN NEOPLASIA", "Neoplasm of Ovary", "Neoplasm of ovary", "ovarian neoplasia", "Neoplasm, Ovarian", "Ovarian Neoplasms", "Ovarian neoplasia", "tumor of the ovary", "Tumor of the Ovary", "Neoplasms, Ovarian", "Ovarian neoplasm NOS", "Neoplasm of the ovary", "neoplasm of the ovary", "Neoplasm of the Ovary", "Neoplasm of the ovaries", "ovary neoplasm (disease)", "Neoplasm of ovary (disorder)", "neoplasm of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian neoplasm", "shortest_name_length": 11}
{"curie": "MONDO:0002260", "names": ["Hidradenitis", "Hydradenitis", "hidradenitis", "HIDRADENITIS", "hydradenitis", "Hidrosadenitis", "hidrosadenitis", "Hidradenitides", "Hydradenitides", "Hidrosadenitides", "apocrine sweat gland", "Apocrine Sweat Gland", "Hidradenitis (disorder)", "Sweat gland inflammation", "apocrine sweat gland inflammation", "inflammation of apocrine sweat gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hidradenitis", "shortest_name_length": 12}
{"curie": "MONDO:0017315", "names": ["Al Gazali-Aziz-Salem syndrome", "Al Gazali Aziz Salem syndrome", "short stature, webbed neck, heart disease", "short stature-webbed neck-heart disease syndrome", "Short stature-webbed neck-heart disease syndrome", "short stature with webbed neck and congenital heart disease syndrome", "Short stature with webbed neck and congenital heart disease syndrome", "Short stature with webbed neck and congenital heart disease syndrome (disorder)", "short stature with webbed neck and congenital heart disease syndrome (diagnosis)", "short stature, intellectual disability, facial dysmorphism, short webbed neck, skin changes and congenital heart disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short stature-webbed neck-heart disease syndrome", "shortest_name_length": 29}
{"curie": "UMLS:C3899282", "names": ["Early Disseminated Lyme Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Early Disseminated Lyme Disease", "shortest_name_length": 31}
{"curie": "MONDO:0007383", "names": ["CDO SYNDROME", "Cdo syndrome", "CDO syndrome", "Corneodermatoosseous syndrome", "CORNEODERMATOOSSEOUS SYNDROME", "CORNEODERMATOOSSEOUS syndrome", "Stern-Lubinsky-Durrie syndrome", "Stern Lubinsky Durrie syndrome", "Corneo-dermato-osseous syndrome", "corneo-dermato-osseous syndrome", "Stern Lubinsky Durrie syndrome (disorder)", "corneal dystrophy epithelial and short stature", "Corneal dystrophy epithelial and short stature", "Corneal dystrophy, epithelial, with skin and skeletal changes", "corneal dystrophy, epithelial, with skin and skeletal changes", "CORNEAL DYSTROPHY, EPITHELIAL, WITH SKIN AND SKELETAL CHANGES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stern-Lubinsky-Durrie syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0100096", "names": ["β-CoV", "β-CoVs", "COVID19", "beta-CoV", "COVID 19", "COVID-19", "2019-nCoV", "beta-CoVs", "SARS-CoV-2", "β-coronavirus", "betacoronavirus", "SARS2 Infection", "SARS-2 Infection", "HCoV-19 Infection", "SARS-CoV2 Disease", "2019-nCoV Disease", "COVID19 (disease)", "2019 nCoV Disease", "2019-nCoV Diseases", "SARS-coronavirus 2", "COVID-19 infection", "COVID-19 Infection", "Disease, 2019-nCoV", "SARS-CoV-2 Disease", "SARS-CoV2 Infection", "2019-nCoV Infection", "2019-nCoV infection", "2019 nCoV Infection", "SARS CoV 2 Infection", "2019-nCoV Infections", "SARS-CoV-2 infection", "SARS-CoV-2 Infection", "Infection, 2019-nCoV", "Infection, SARS-CoV-2", "SARS-CoV-2 Infections", "coronavirus 2019-nCoV", "COVID-19 Virus Disease", "Coronavirus Disease 19", "2019 novel coronavirus", "COVID 19 Virus Disease", "Coronavirus Disease-19", "COVID-19 Virus Diseases", "Disease, COVID-19 Virus", "Virus Disease, COVID-19", "COVID-19 Virus Infection", "Coronavirus disease 2019", "COVID 19 Virus Infection", "Coronavirus Disease 2019", "coronavirus disease 2019", "COVID-19 Virus Infections", "Infection, COVID-19 Virus", "Disease 2019, Coronavirus", "Virus Infection, COVID-19", "Wuhan coronavirus infection", "Disease caused by 2019-nCoV", "SARS Coronavirus 2 Infection", "Disease caused by SARS-CoV-2", "COVID-19 infection (diagnosis)", "2019 Novel Coronavirus Disease", "coronavirus 2019-nCoV infection", "2019 Novel Coronavirus Infection", "Human Coronavirus 2019 Infection", "2019 novel coronavirus infection", "2019 Novel Coronavirus (2019-nCoV)", "COVID-19 (Coronavirus Disease 2019)", "Disease caused by 2019 novel coronavirus", "Wuhan seafood market pneumonia virus infection", "severe acute respiratory syndrome coronavirus 2", "Severe Acute Respiratory Syndrome Coronavirus 2 Infection", "Disease caused by severe acute respiratory syndrome coronavirus 2", "severe acute respiratory syndrome coronavirus 2 infectious disease", "Disease caused by severe acute respiratory syndrome coronavirus 2 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "COVID-19", "shortest_name_length": 5}
{"curie": "MONDO:0009219", "names": ["Congenital fascial dystrophy", "congenital fascial dystrophy", "Fascial Dystrophy, Congenital", "fascial dystrophy, congenital", "FASCIAL DYSTROPHY, CONGENITAL", "congenital fascial dystrophy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fascial dystrophy, congenital", "shortest_name_length": 28}
{"curie": "UMLS:C4552208", "names": ["Trichoblastic Carcinoma", "Trichoblastic carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Trichoblastic carcinoma", "shortest_name_length": 23}
{"curie": "MONDO:0019312", "names": ["HPS", "h s p", "h p s", "H.P.S.", "Hermansky-Pudlak", "Hermansky-Pudlak Syndrome", "Hermansky Pudlak Syndrome", "hermanski-pudlak syndrome", "Hermanski-Pudlak Syndrome", "hermansky pudlak syndrome", "Hermanski Pudlak Syndrome", "Hermansky-Pudlak syndrome", "hermansky-pudlak syndrome", "Hermansky Pudlak syndrome", "Alpha storage pool disease", "HPS (Hermansky Pudlak syndrome)", "Albinism with hemorrhagic diathesis", "Albinism with haemorrhagic diathesis", "Hermansky-Pudlak syndrome (disorder)", "Hermansky-Pudlak syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hermansky-Pudlak syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C5670392", "names": ["Articulated Supernumerary Rib", "SUPERNUMERARY RIB, ARTICULATED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Articulated Supernumerary Rib", "shortest_name_length": 29}
{"curie": "MONDO:0012326", "names": ["DFNB42", "autosomal recessive deafness 42", "DEAFNESS, AUTOSOMAL RECESSIVE 42", "deafness, autosomal recessive 42", "Deafness, Autosomal Recessive 42", "deafness, autosomal recessive type 42", "DEAFNESS, AUTOSOMAL RECESSIVE 42 (disorder)", "autosomal recessive nonsyndromic deafness 42", "ILDR1 autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 42", "autosomal recessive nonsyndromic deafness type 42", "autosomal recessive nonsyndromic deafness caused by mutation in ILDR1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 42", "shortest_name_length": 6}
{"curie": "MONDO:0016048", "names": ["Isolated autosomal dominant hypomagnesemia Glaudemans type", "Isolated autosomal dominant hypomagnesemia, Glaudemans type", "isolated autosomal dominant hypomagnesemia, Glaudemans type", "Isolated autosomal dominant hypomagnesaemia Glaudemans type", "Isolated autosomal dominant hypomagnesemia Glaudemans type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated autosomal dominant hypomagnesemia, Glaudemans type", "shortest_name_length": 58}
{"curie": "UMLS:C1335505", "names": ["PROSTATE CANCER METASTATIC BONE", "Prostate Carcinoma Metastatic in the Bone", "Prostate Carcinoma Metastatic to the Bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Carcinoma Metastatic in the Bone", "shortest_name_length": 31}
{"curie": "UMLS:C4087241", "names": ["Frustration tolerance decreased"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Frustration tolerance decreased", "shortest_name_length": 31}
{"curie": "UMLS:C0026865", "names": ["Mycetism", "MYCETISMUS", "mycetismus", "poisoning mushroom", "mushroom poisoning", "MUSHROOM POISONING", "Mushroom poisoning", "Mushroom Poisoning", "Mushroom Poisonings", "TOADSTOOL, TOXICITY", "Poisoning, Mushroom", "poisoning; mushrooms", "Poisonings, Mushroom", "mushrooms; poisoning", "Mushroom intoxication", "toxicity to mushrooms", "food toxicity to mushrooms", "Mushroom poisoning syndrome", "Mushrooms causing toxic effect", "toxicity to mushrooms (diagnosis)", "Toxic effect from eating mushrooms", "Toxic effect of ingested mushrooms", "Toxic effect of ingested mushrooms NOS", "Toxic effect of mushrooms eaten as food", "Toxic effect from eating mushrooms (disorder)", "poisoning; food, noxious or naturally toxic, mushrooms", "food; poisoning, noxious or naturally toxic, mushrooms"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mushroom Poisoning", "shortest_name_length": 8}
{"curie": "UMLS:C0151449", "names": ["primary Sjogren syndrome", "Primary Sjögren Syndrome", "Primary Sjogren Syndrome", "Primary Sjögren syndrome", "primary sjogren's syndrome", "Primary Sjogren's syndrome", "Primary Sjögren's syndrome", "Sjogren's syndrome, primary", "Sjogren's Syndrome, Primary", "Primary Sjögren-Gougerot syndrome", "primary Sjogren syndrome (diagnosis)", "Primary Sjögren's syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Sjögren's syndrome", "shortest_name_length": 24}
{"curie": "MONDO:0018687", "names": ["PMA", "Cruveilhier", "Duchenne-Aran", "Duchenne-Aran; atrophy", "atrophy; Duchenne-Aran", "Progressive muscular atrophy", "progressive muscular atrophy", "Progressive Muscular Atrophy", "Muscular Atrophy, Progressive", "Atrophy, Progressive Muscular", "muscle; atrophy, Duchenne-Aran", "Progressive Muscular Atrophies", "atrophy; muscle, Duchenne-Aran", "Duchenne-Aran muscular atrophy", "Atrophies, Progressive Muscular", "Muscular Atrophies, Progressive", "Pure progressive muscular atrophy", "pure progressive muscular atrophy", "PMA - Progressive muscular atrophy", "progressive spinal muscular atrophy", "Progressive muscular atrophy (disorder)", "Progressive Myelopathic Muscular Atrophy", "progressive muscular atrophy (diagnosis)", "Myelopathic Muscular Atrophy, Progressive", "Duchenne-Aran muscular atrophy (diagnosis)", "progressive muscular atrophy (Duchenne-Aran)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive muscular atrophy", "shortest_name_length": 3}
{"curie": "UMLS:C4526726", "names": ["Stage IVA Lung Cancer", "Stage IVA Lung Cancer AJCC v8", "stage IVA lung cancer AJCC v8", "stage IVA non-small cell lung cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Lung Cancer AJCC v8", "shortest_name_length": 21}
{"curie": "MONDO:0002907", "names": ["Cerebral Thrombosis", "cerebral thrombosis", "Thrombosis cerebral", "CEREBRAL THROMBOSIS", "thrombosis cerebral", "THROMBOSIS CEREBRAL", "Cerebral Thromboses", "Cerebral thrombosis", "cerebral; thrombosis", "Thromboses, Cerebral", "THROMBOSIS, CEREBRAL", "Thrombosis, Cerebral", "thrombosis; cerebral", "Intracranial Thrombus", "Thrombus, Intracranial", "Intracranial Thrombosis", "Intracranial Thromboses", "intracranial thrombosis", "Cerebral thrombosis NOS", "Intracranial thrombosis", "thrombosis; intracranial", "intracranial; thrombosis", "Thromboses, Intracranial", "CT - Cerebral thrombosis", "Thrombosis, Intracranial", "cerebral artery thrombosis", "Thrombosis;artery;cerebral", "Cerebral artery thrombosis", "thrombosis; cerebral artery", "THROMBOSIS CEREBRAL ARTERIAL", "cerebral arterial thrombosis", "CEREBRAL ARTERIAL THROMBOSIS", "Thrombosis cerebral arterial", "Cerebral arterial thrombosis", "thrombosis of cerebral artery", "Thrombosis of cerebral arteries", "cerebral artery thrombosis (diagnosis)", "Cerebral arterial thrombosis (disorder)", "Cerebral thrombosis (vessel unspecified)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intracranial thrombosis", "shortest_name_length": 19}
{"curie": "MONDO:0013285", "names": ["CVID5", "common variable immunodeficiency 5", "immunodeficiency, common variable, 5", "IMMUNODEFICIENCY, COMMON VARIABLE, 5", "MS4A1 common variable immunodeficiency", "ANTIBODY DEFICIENCY DUE TO CD20 DEFECT", "antibody deficiency due to CD20 defect", "immunodeficiency, common variable, type 5", "common variable immunodeficiency caused by mutation in MS4A1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency, common variable, 5", "shortest_name_length": 5}
{"curie": "MONDO:0024612", "names": ["Manic Disorder", "MANIC DISORDER", "manic disorder", "manic disorders", "Manic Disorders", "disorder; manic", "manic; disorder", "monopolar mania", "Disorder, Manic", "bipolar disorder manic", "BIPOLAR DISEASE, MANIC", "BIPOLAR DISORDER, MANIC", "Manic bipolar I disorder", "CYCLOTHYMIC DISORDER, MANIC", "manic-depressive - now manic", "Manic-depressive - now manic", "bipolar disorder manic phase", "Manic bipolar I disorder, NOS", "bipolar depression manic phase", "manic bipolar affective disorder", "Manic Bipolar Affective Disorder", "Bipolar affective disorder, manic", "BIPOLAR DISORDER MANIC UNSPECIFIED", "Manic bipolar I disorder (disorder)", "MANIC DEPRESSIVE DISEASE MANIC PHASE", "MANIC DEPRESSIVE DISEASE, MANIC PHASE", "Bipolar I disorder, most recent episode manic", "bipolar I disorder, most recent episode, manic", "disorder; bipolar, I, most recent episode, manic", "Bipolar affective disorder, current episode manic", "bipolar disorder affective, current episode manic", "bipolar affective disorder, current episode manic", "disorder; bipolar, affective, current episode, manic", "Bipolar affective disorder, manic, unspecified degree", "Bipolar I disorder, most recent episode manic (disorder)", "bipolar I disorder, most recent episode, manic (diagnosis)", "Bipolar affective disorder, current episode manic (disorder)", "Bipolar affective disorder, current episode manic (diagnosis)", "Bipolar I disorder, Current or most recent episode manic, Unspecified", "Bipolar I disorder, most recent episode (or current) manic, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "manic bipolar affective disorder", "shortest_name_length": 14}
{"curie": "UMLS:C1142159", "names": ["Intentional misuse"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intentional misuse", "shortest_name_length": 18}
{"curie": "UMLS:C2347613", "names": ["Atypical Teratoid/Rhabdoid Tumor", "childhood atypical teratoid/rhabdoid tumor", "Childhood Atypical Teratoid/Rhabdoid Tumor", "childhood rhabdoid tumor of the central nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Atypical Teratoid/Rhabdoid Tumor", "shortest_name_length": 32}
{"curie": "MONDO:0014197", "names": ["IMD12", "immunodeficiency 12", "IMMUNODEFICIENCY 12", "immunodeficiency type 12", "combined immunodeficiency due to MALT1 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined immunodeficiency due to MALT1 deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0007623", "names": ["FLUSHING OF EARS AND SOMNOLENCE", "flushing of ears and somnolence"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "flushing of ears and somnolence", "shortest_name_length": 31}
{"curie": "MONDO:0016894", "names": ["partial monosomy of chromosome 16p", "partial deletion of chromosome 16p", "partial deletion of the short arm of chromosome 16", "partial monosomy of the short arm of chromosome 16", "partial deletion of the short arm of chromosome type 16"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of the short arm of chromosome 16", "shortest_name_length": 34}
{"curie": "MONDO:0019272", "names": ["Hereditary PPK", "hereditary PPK", "hereditary palmoplantar keratosis", "Hereditary keratosis palmoplantaris", "hereditary palmoplantar keratoderma", "hereditary keratosis palmoplantaris", "Hereditary palmoplantar keratoderma", "Hereditary palmoplantar hyperkeratosis", "hereditary palmoplantar hyperkeratosis", "Hereditary palmoplantar keratoderma (disorder)", "hereditary palmoplantar keratoderma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary palmoplantar keratoderma", "shortest_name_length": 14}
{"curie": "MONDO:0010791", "names": ["Myoglobinuria, episodic", "myoglobinuria recurrent", "Recurrent myoglobinuria", "Myoglobinuria, recurrent", "Myoglobinuria, Recurrent", "myoglobinuria, recurrent", "MYOGLOBINURIA, RECURRENT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myoglobinuria, recurrent", "shortest_name_length": 23}
{"curie": "UMLS:C0027046", "names": ["heart; degeneration", "degeneration; heart", "Degeneration of heart", "Myocardial Degeneration", "Degeneration myocardial", "DEGENERATION MYOCARDIAL", "myocardial degeneration", "Myocardial degeneration", "degeneration; myocardial", "myocardium; degeneration", "Mural degeneration of heart", "muscle; degeneration, heart", "degeneration; muscle, heart", "Muscular degeneration of heart", "Myocardial degeneration (disorder)", "myocardial degeneration (diagnosis)", "Mural degeneration of heart or myocardium", "Muscular degeneration of heart or myocardium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myocardial degeneration", "shortest_name_length": 19}
{"curie": "UMLS:C0948353", "names": ["Markedly reduced dietary intake"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Markedly reduced dietary intake", "shortest_name_length": 31}
{"curie": "MONDO:0013051", "names": ["ARCL2B", "cutis laxa type IIB", "ARCL2, progeroid type", "cutis laxa type IIB (diagnosis)", "Cutis Laxa With Progeroid Features", "CUTIS LAXA WITH PROGEROID FEATURES", "cutis laxa with progeroid features", "autosomal recessive cutis laxa type 2B", "Autosomal recessive cutis laxa type 2B", "autosomal recessive cutis laxa type IIB", "cutis laxa, autosomal recessive type 2B", "cutis laxa, autosomal recessive, type 2B", "cutis laxa, autosomal recessive, type IIB", "CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIB", "Cutis Laxa, Autosomal Recessive, Type IIB", "PYCR1 autosomal recessive cutis laxa type 2", "ARCL2B - autosomal recessive cutis laxa type 2B", "Autosomal recessive cutis laxa type 2B (disorder)", "Autosomal recessive cutis laxa type 2 progeroid type", "autosomal recessive cutis laxa type 2, progeroid type", "Autosomal recessive cutis laxa type 2, progeroid type", "autosomal recessive cutis laxa type 2 caused by mutation in PYCR1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive cutis laxa type 2B", "shortest_name_length": 6}
{"curie": "MONDO:0014046", "names": ["CWS4", "Cowden syndrome 4", "COWDEN SYNDROME 4", "KLLN Cowden disease", "Cowden syndrome type 4", "Cowden disease caused by mutation in KLLN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cowden syndrome 4", "shortest_name_length": 4}
{"curie": "UMLS:C0276919", "names": ["Roundworm infection", "Intestinal Nematode Infection", "intestinal nematode infection", "Intestinal nematode infection", "Intestinal roundworm infection", "Intestinal nematode infection, NOS", "Intestinal nematode infection (disorder)", "intestinal nematode infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal nematode infection", "shortest_name_length": 19}
{"curie": "UMLS:C4683614", "names": ["Lugano Classification Stage IV Adult Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage IV Adult Hodgkin Lymphoma AJCC v8", "shortest_name_length": 61}
{"curie": "UMLS:C4330510", "names": ["KATP-Associated Hyperinsulinism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "KATP-Associated Hyperinsulinism", "shortest_name_length": 31}
{"curie": "UMLS:C1336171", "names": ["Stage IIA Retinoblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Retinoblastoma", "shortest_name_length": 24}
{"curie": "MONDO:0000514", "names": ["bone squamous cell carcinoma", "bone tissue squamous cell carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bone squamous cell carcinoma", "shortest_name_length": 28}
{"curie": "UMLS:C4726631", "names": ["Refractory Head and Neck Cancer", "Refractory Malignant Head and Neck Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Malignant Head and Neck Neoplasm", "shortest_name_length": 31}
{"curie": "MONDO:0003754", "names": ["Hemicord syndrome", "HEMICORD SYNDROME", "Hemicord Syndrome", "Syndrome, Hemicord", "Hemicord Syndromes", "Syndromes, Hemicord", "Brown-Sequard Disease", "brown-sequard disease", "Brown Sequard Disease", "Brown-Squard syndrome", "brown sequard syndrome", "brown-sequard syndrome", "Brown-Sequard syndrome", "BROWN-SEQUARD SYNDROME", "Brown-Séquard syndrome", "Brown-Sequards Disease", "BROWN SEQUARD SYNDROME", "Brown-Sequard Syndrome", "Brown Sequard Syndrome", "Brown Sequard's Disease", "Hemiparaplegic Syndrome", "HEMIPARAPLEGIC SYNDROME", "Hemiparaplegic syndrome", "Brown-Sequard's Disease", "brown-sequards syndrome", "Syndrome, Brown-Sequard", "Brown-Sequards Syndrome", "brown sequards syndrome", "brown-sequard's syndrome", "Hemispinal cord syndrome", "browns disease sequard's", "Syndrome, Hemiparaplegic", "Hemispinal Cord Syndrome", "Brown Sequard's Syndrome", "Hemiparaplegic Syndromes", "Brown-Sequard's Syndrome", "Syndrome, Brown-Sequard's", "Syndromes, Hemiparaplegic", "Hemispinal Cord Syndromes", "Syndrome, Hemispinal Cord", "Syndromes, Hemispinal Cord", "Brown-Séquard syndrome (disorder)", "Brown-Sequard syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brown-Sequard syndrome", "shortest_name_length": 17}
{"curie": "UMLS:C0279096", "names": ["pediatric AML in remission", "Pediatric AML in Remission", "Childhood AML in Remission", "childhood AML in remission", "childhood ANLL in remission", "AML, childhood in remission", "pediatric ANLL in remission", "AML, pediatric in remission", "ANLL, childhood in remission", "ANLL, pediatric in remission", "Acute Myeloid Leukemia (AML) in Remission", "remission, childhood myeloid acute leukemia", "childhood acute myeloid leukemia in remission", "Pediatric Acute Myeloid Leukemia in Remission", "pediatric acute myeloid leukemia in remission", "Childhood Acute Myeloid Leukemia in Remission", "childhood leukemia, acute myeloid in remission", "acute myeloid leukemia in remission, childhood", "pediatric leukemia, acute myeloid in remission", "nonlymphocytic leukemia in remission, childhood", "Pediatric Acute Myelocytic Leukemia in Remission", "Childhood Acute Myelocytic Leukemia in Remission", "Childhood Acute Myelogenous Leukemia in Remission", "Pediatric Acute Myelogenous Leukemia in Remission", "remission, childhood nonlymphocytic acute leukemia", "Childhood Acute Granulocytic Leukemia in Remission", "Pediatric Acute Granulocytic Leukemia in Remission", "Pediatric Acute Myeloblastic Leukemia in Remission", "Childhood Acute Myeloblastic Leukemia in Remission", "pediatric acute nonlymphocytic leukemia in remission", "childhood acute nonlymphocytic leukemia in remission", "acute nonlymphocytic leukemia in remission, childhood", "childhood leukemia, acute nonlymphocytic in remission", "pediatric leukemia, acute nonlymphocytic in remission"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Acute Myeloid Leukemia in Remission", "shortest_name_length": 26}
{"curie": "UMLS:C0586370", "names": ["Rectal dysplasia", "Rectal Dysplasia", "Dysplasia of Rectum", "Dysplasia of rectum", "Dysplasia of the Rectum", "Dysplasia of rectum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dysplasia of rectum", "shortest_name_length": 16}
{"curie": "MONDO:0000456", "names": ["CDS", "CCDS", "creatine deficiency syndrome", "cerebral creatine deficiency syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral creatine deficiency syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0024308", "names": ["PXE", "pseudoxanthoma elasticum", "pseudoxanthoma elasticum (inherited or acquired)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudoxanthoma elasticum (inherited or acquired)", "shortest_name_length": 3}
{"curie": "MONDO:0018269", "names": ["white platelet syndrome", "White platelet syndrome", "White platelet syndrome (disorder)", "platelet granule deficiency disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "white platelet syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0020646", "names": ["OAL", "Ocular Adnexal Lymphoma", "ocular adnexal lymphoma", "Primary Ocular Adnexal Lymphoma", "ocular adnexa non-Hodgkin lymphoma", "Ocular Adnexal Non-Hodgkin Lymphoma", "non-Hodgkin lymphoma of ocular adnexa", "Primary Ocular Adnexal Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ocular adnexal lymphoma", "shortest_name_length": 3}
{"curie": "MONDO:0035689", "names": ["syndrome of reduced sensitivity to thyroid hormone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndrome of reduced sensitivity to thyroid hormone", "shortest_name_length": 50}
{"curie": "MONDO:0005361", "names": ["EE", "EoE", "Eosinophilic Esophagitis", "Eosinophilic esophagitis", "eosinophilic esophagitis", "Esophagitis, Eosinophilic", "eosinophilic oesophagitis", "ESOPHAGITIS, EOSINOPHILIC", "Eosinophilic Oesophagitis", "Eosinophilic oesophagitis", "Esophagitis, eosinophilic", "Eosinophilic Esophagitides", "Esophagitides, Eosinophilic", "Eosinophilic Chronic Esophagitis", "Chronic Esophagitis, Eosinophilic", "Esophagitis, Eosinophilic Chronic", "Eosinophilic Chronic Esophagitides", "Esophagitides, Eosinophilic Chronic", "Eosinophilic esophagitis (disorder)", "Chronic Esophagitides, Eosinophilic", "eosinophilic esophagitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eosinophilic esophagitis", "shortest_name_length": 2}
{"curie": "UMLS:C5418809", "names": ["Advanced Endometrial Adenocarcinoma", "Advanced Endometrial Adenocarcinoma, NOS", "Advanced Endometrial Adenocarcinoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Endometrial Adenocarcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C1335714", "names": ["Recurrent Neck Squamous Cell CUP", "Recurrent Neck Squamous Cell Carcinoma of Unknown Primary", "Relapsed Metastatic Epidermoid Carcinoma to the Neck with Occult Primary", "Recurrent Metastatic Epidermoid Carcinoma to the Neck with Occult Primary", "Recurrent Metastatic Squamous Cell Cancer to the Neck with Occult Primary", "Relapsed Metastatic Squamous Cell Carcinoma to the Neck with Occult Primary", "Recurrent Metastatic Squamous Cell Carcinoma in the Neck with Occult Primary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Neck Squamous Cell Carcinoma of Unknown Primary", "shortest_name_length": 32}
{"curie": "UMLS:C5446559", "names": ["Lacrimal System Lymphoma", "Primary Lacrimal System Lymphoma", "Lacrimal System Non-Hodgkin Lymphoma", "Primary Lacrimal System Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lacrimal System Non-Hodgkin Lymphoma", "shortest_name_length": 24}
{"curie": "MONDO:0011124", "names": ["SEMDAD", "spondyloepimetaphyseal dysplasia with abnormal dentition", "Spondyloepimetaphyseal Dysplasia With Abnormal Dentition", "SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH ABNORMAL DENTITION", "spondyloepimetaphyseal dysplasia-abnormal dentition syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepimetaphyseal dysplasia-abnormal dentition syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0013737", "names": ["SPG46", "hereditary spastic paraplegia 46", "hereditary spastic paraplegia type 46", "autosomal recessive spastic paraplegia 46", "SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE", "spastic paraplegia 46, autosomal recessive", "Autosomal recessive spastic paraplegia type 46", "autosomal recessive spastic paraplegia type 46", "GBA2 autosomal recessive complex spastic paraplegia", "familial spastic paraplegia autosomal recessive type 46", "Autosomal recessive spastic paraplegia type 46 (disorder)", "Autosomal recessive spastic paraplegia type 46 (diagnosis)", "autosomal recessive complex spastic paraplegia caused by mutation in GBA2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 46", "shortest_name_length": 5}
{"curie": "UMLS:C4725024", "names": ["Advanced Leukemia", "Refractory Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Leukemia", "shortest_name_length": 17}
{"curie": "UMLS:C1394320", "names": ["Endometrial cyst", "Endometrial Cyst", "cyst; endometrial", "endometrium; cyst", "Cyst of endometrium", "Cyst of endometrium (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cyst of endometrium", "shortest_name_length": 16}
{"curie": "MONDO:0009505", "names": ["DLACD", "GOUT5", "UAQTL7", "D-LACTIC ACIDURIA", "GOUT, SUSCEPTIBILITY TO, 5", "D-LACTIC ACIDURIA AND GOUT", "D-LACTIC ACIDURIA WITH GOUT", "lactic aciduria due to D-lactic acid", "Lactic Aciduria due to D-Lactic Acid", "D-lactic aciduria with susceptibility to gout", "URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lactic aciduria due to D-lactic acid", "shortest_name_length": 5}
{"curie": "MONDO:0001495", "names": ["hematocele", "Hematocele", "Haematocele", "Hematoceles", "Haematocoele", "haematocoele", "male hematocele", "Male hematocele", "hematocele; male", "Male haematocele", "Hematocele NOS, male", "Male hematocele (disorder)", "Effusion of blood into cavity", "Hematocele (morphologic abnormality)", "Hematocele of tunica vaginalis testis", "hematocele of tunica vaginalis testis", "Haematocele of tunica vaginalis testis", "Haematocoele of tunica vaginalis testis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hematocele of tunica vaginalis testis", "shortest_name_length": 10}
{"curie": "UMLS:C4054724", "names": ["Infiltrating Intramuscular Lipoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infiltrating Intramuscular Lipoma", "shortest_name_length": 33}
{"curie": "MONDO:0019835", "names": ["primary hypophysitis", "Primary hypophysitis", "Lymphoid Hypophysitis", "Hypophysitis, Lymphoid", "autoimmune hypophysitis", "Lymphoid Hypophysitides", "Autoimmune hypophysitis", "Autoimmune Hypophysitis", "lymphocytic hypophysitis", "Lymphocytic Hypophysitis", "Hypophysitides, Lymphoid", "Hypophysitis, Autoimmune", "Autoimmune Hypophysitides", "Hypophysitis, Lymphocytic", "Lymphocytic Hypophysitides", "Hypophysitides, Autoimmune", "Hypophysitides, Lymphocytic", "Autoimmune hypophysitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary hypophysitis", "shortest_name_length": 20}
{"curie": "MONDO:0010106", "names": ["testes, rudimentary", "TESTES, RUDIMENTARY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testes, rudimentary", "shortest_name_length": 19}
{"curie": "MONDO:0021452", "names": ["benign cornea tumor", "Benign Cornea Tumor", "benign corneal tumor", "Benign Corneal Tumor", "benign cornea neoplasm", "Benign tumor of cornea", "cornea benign neoplasm", "Benign Cornea Neoplasm", "Benign Tumor of Cornea", "benign tumor of cornea", "benign corneal neoplasm", "Benign tumour of cornea", "Benign Corneal Neoplasm", "benign neoplasm of cornea", "Benign Neoplasm of Cornea", "Benign neoplasm of cornea", "benign tumor of the cornea", "Benign Tumor of the Cornea", "benign neoplasm of the cornea", "Benign Neoplasm of the Cornea", "Benign neoplasm of cornea (disorder)", "benign neoplasm of cornea (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of cornea", "shortest_name_length": 19}
{"curie": "UMLS:C4687546", "names": ["Metastatic Urogenital Carcinoma", "Metastatic Genitourinary Cancer", "Metastatic Genitourinary Carcinoma", "Metastatic Genitourinary System Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Genitourinary System Carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0018581", "names": ["PER", "perm", "PERM", "Progressive Encephalomyelitis with Rigidity", "PROGRESSIVE ENCEPHALOMYELITIS WITH RIGIDITY", "Progressive encephalomyelitis with rigidity and myoclonus", "progressive encephalomyelitis with rigidity and myoclonus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive encephalomyelitis with rigidity and myoclonus", "shortest_name_length": 3}
{"curie": "MONDO:0006642", "names": ["dts", "DTS", "DTs", "DELERIUM TREMENS", "delirium tremens", "Delirium tremens", "delirium Tremens", "delerium tremens", "DELIRIUM TREMENS", "Delirium Tremens", "tremens; delirium", "alcohol; delirium", "delirium; alcohol", "deliriums tremens", "delirium; tremens", "ALCOHOLIC DELIRIUM", "Alcoholic delirium", "DELIRIUM, ALCOHOLIC", "DTs - delirium tremens", "Delirium tremens;alcoholic", "alcohol withdrawal delirium", "Alcohol withdrawal delirium", "Alcohol Withdrawal Delirium", "Delirium, Alcohol Withdrawal", "delirium, alcohol withdrawal", "alcohol; delirium, withdrawal", "alcohol withdrawal hallucinosis", "hallucinosis, alcohol withdrawal", "alcohol withdrawal with delirium", "alcohol; withdrawal, with delirium", "withdrawal; alcohol, with delirium", "ALCOHOL WITHDRAWAL DELIRIUM TREMENS", "delirium; alcohol, due to withdrawal", "Alcohol withdrawal delirium (disorder)", "alcohol; withdrawal state with delirium", "alcohol withdrawal delirium (diagnosis)", "withdrawal state; alcohol, with delirium", "alcohol withdrawal-induced delirium Tremens", "Alcohol Withdrawal-Induced Delirium Tremens", "syndrome; alcohol withdrawal, with delirium", "Alcohol Withdrawal Induced Delirium Tremens", "alcohol; withdrawal syndrome, with delirium", "alcohol withdrawal induced delirium Tremens", "Delirium Tremens, Alcohol Withdrawal Induced", "delirium Tremens, alcohol withdrawal induced", "alcohol withdrawal associated autonomic hyperactivity", "intoxication; alcohol, withdrawal state, with delirium", "alcohol; intoxication, withdrawal state, with delirium", "autonomic hyperactivity, alcohol withdrawal associated", "Mental and behavioral disorders due to use of alcohol, withdrawal state with delirium", "Mental and behavioural disorders due to use of alcohol, withdrawal state with delirium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alcohol withdrawal delirium", "shortest_name_length": 3}
{"curie": "MONDO:0100284", "names": ["X-linked intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability", "shortest_name_length": 32}
{"curie": "MONDO:0019468", "names": ["TPLL", "T-PLL", "T-Cell CLL", "T Cell CLL", "T cell CLL", "T-cell CLL", "CLL, T-Cell", "CLL, T-cell", "chronic T-cell leukemia", "Chronic T-Cell Leukemia", "T-Cell Leukemia, Chronic", "Leukemias chronic T-cell", "Leukemia, T-Cell, Chronic", "Leukaemias chronic T-cell", "T prolymphocytic leukemia", "leukemia, T-cell, chronic", "T Prolymphocytic Leukemia", "Leukemia, T Cell, Chronic", "T-Cell Prolymphocytic Leukemia", "T-cell prolymphocytic leukemia", "T Cell Prolymphocytic Leukemia", "T cell prolymphocytic leukemia", "T-Lymphocytic Leukemia, Chronic", "T-cell prolymphocytic leukaemia", "Leukemia, T-Cell Prolymphocytic", "Prolymphocytic Leukemia, T-Cell", "T-Cell Prolymphocytic Leukemias", "Leukemia, Prolymphocytic, T-Cell", "Leukemias, T-Cell Prolymphocytic", "Prolymphocytic Leukemias, T-Cell", "T cell chronic lymphocytic leukemia", "T-Cell Chronic Lymphocytic Leukemia", "Chronic T-Cell Lymphocytic Leukemia", "T Cell Chronic Lymphocytic Leukemia", "chronic T-cell lymphocytic leukemia", "T-cell chronic lymphocytic leukemia", "Prolymphocytic leukemia, T-cell type", "T-cell chronic lymphocytic leukaemia", "Lymphocytic Leukemia, T-Cell, Chronic", "Lymphocytic Leukemia, T Cell, Chronic", "Prolymphocytic leukaemia, T-cell type", "Leukemia, Lymphocytic, Chronic, T-Cell", "Prolymphocytic leukemia of T-cell type", "Leukemia, Lymphocytic, Chronic, T Cell", "T-cell prolymphocytic leukemia (disorder)", "T-cell prolymphocytic leukemia (diagnosis)", "TCLL - T-cell chronic lymphocytic leukemia", "Prolymphocytic leukemia of T-cell type NOS", "TCLL - T-cell chronic lymphocytic leukaemia", "T-cell chronic lymphocytic leukemia (disorder)", "chronic T-cell lymphocytic leukemia (diagnosis)", "Prolymphocytic leukemia, T-cell type (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-cell prolymphocytic leukemia", "shortest_name_length": 4}
{"curie": "UMLS:C5446518", "names": ["Recurrent Acral Lentiginous Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Acral Lentiginous Melanoma", "shortest_name_length": 36}
{"curie": "UMLS:C0281328", "names": ["Subependymoma", "Adult Subependymoma", "adult subependymoma", "subependymoma, adult", "Adult Subependymal Astrocytoma", "adult subependymal astrocytoma", "Astrocytoma, Adult Subependymal", "Subependymal Astrocytoma, Adult", "Adult Subependymal Astrocytomas", "Subependymal Astrocytomas, Adult", "Astrocytomas, Adult Subependymal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Subependymoma", "shortest_name_length": 13}
{"curie": "UMLS:C1518726", "names": ["Ovarian Mucinous Cystic Tumor Associated with Pseudomyxoma Peritonei"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Mucinous Cystic Tumor Associated with Pseudomyxoma Peritonei", "shortest_name_length": 68}
{"curie": "UMLS:C4055127", "names": ["Dislodged Catheter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dislodged Catheter", "shortest_name_length": 18}
{"curie": "MONDO:0003714", "names": ["bladder urachal squamous cell carcinoma", "Bladder Urachal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder urachal squamous cell carcinoma", "shortest_name_length": 39}
{"curie": "UMLS:C0346091", "names": ["Cockade Nevus", "Cockade nevus", "Cockade naevus", "Cockade nevus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cockade nevus", "shortest_name_length": 13}
{"curie": "UMLS:C5556835", "names": ["Hybrid Salivary Gland Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hybrid Salivary Gland Carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0003542", "names": ["Denticle", "Denticles", "denticles", "Pulp stone", "Pulpoliths", "Pulp Stone", "pulp stone", "Stone, Pulp", "Pulp stones", "PULP STONES", "pulp stones", "Pulp Stones", "Stones, Pulp", "True denticles", "Pulp denticles", "False denticles", "True pulp stones", "False pulp stones", "Dental pulp stone", "Dental Pulp Stone", "dental pulp stones", "pulp calcification", "Stone, Dental Pulp", "Dental Pulp Stones", "Pulp calcification", "Pulp Stone, Dental", "calcification pulp", "Dental pulp stones", "Pulp calcifications", "Stones, Dental Pulp", "calcification; pulp", "Pulp Stones, Dental", "pulp calcifications", "pulp; calcification", "Denticles (disorder)", "denticles (diagnosis)", "pulpal calcifications", "Pulpal calcifications", "pulpal; calcification", "calcification; pulpal", "Pulp stone (disorder)", "Dental Pulp Calcification", "dental pulp calcification", "Dental Pulp Calcifications", "Calcification, Dental Pulp", "Pulp Calcification, Dental", "Calcifications, Dental Pulp", "Pulp Calcifications, Dental"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dental pulp calcification", "shortest_name_length": 8}
{"curie": "MONDO:0007808", "names": ["IHCM", "ichthyosis hystrix of Curth-Macklin", "Ichthyosis hystrix of Curth-Macklin", "Curth-Macklin type ichthyosis hystrix", "Ichthyosis Hystrix, Curth-Macklin Type", "Ichthyosis hystrix, Curth-Macklin type", "ichthyosis histrix, curth-macklin type", "ICHTHYOSIS HYSTRIX, CURTH-MACKLIN TYPE", "Ichthyosis hystrix, Curth Macklin type", "ichthyosis HYSTRIX, Curth-Macklin type", "ichthyosis hystrix, Curth Macklin type", "ichthyosis hystrix, Curth-Macklin type", "Ichthyosis hystrix of Curth-Macklin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ichthyosis hystrix of Curth-Macklin", "shortest_name_length": 4}
{"curie": "UMLS:C4054537", "names": ["PLA2R Induced Membranous Nephropathy", "Membranous Nephropathy - PLA2R Induced", "Phospholipase 2 Receptor Membranous Nephropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Membranous Nephropathy - PLA2R Induced", "shortest_name_length": 36}
{"curie": "MONDO:0009309", "names": ["CGD1", "CDG1", "SOC2 DEFICIENCY", "NCF1 DEFICIENCY", "deficiency of NCF1", "deficiency of SOC2", "Soc2, deficiency of", "p47-PHOX DEFICIENCY", "Ncf1, deficiency of", "deficiency of p47-PHOX", "P47-Phox, Deficiency of", "p47-PHOX, deficiency of", "NCF1 chronic granulomatous disease", "NEUTROPHIL CYTOSOL FACTOR 1 DEFICIENCY", "SOLUBLE OXIDASE COMPONENT II DEFICIENCY", "deficiency of neutrophil cytosol factor 1", "neutrophil cytosol Factor 1, deficiency of", "deficiency of soluble oxidase component II", "Neutrophil Cytosol Factor 1, Deficiency of", "Soluble Oxidase Component II, Deficiency of", "soluble oxidase component II, deficiency of", "autosomal recessive chronic granulomatous disease 1", "chronic granulomatous disease 1, autosomal recessive", "CGD, autosomal recessive cytochrome B-positive, type 1", "Granulomatous Disease, Chronic, due to NCF1 Deficiency", "GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, 1", "GRANULOMATOUS DISEASE, CHRONIC, DUE TO NCF1 DEFICIENCY", "granulomatous disease, chronic, due to Ncf1 deficiency", "CGD, Autosomal Recessive Cytochrome B-Positive, Type I", "CGD, AUTOSOMAL RECESSIVE CYTOCHROME b-POSITIVE, TYPE I", "chronic granulomatous disease due to deficiency of NCF-1", "Chronic Granulomatous Disease due to Deficiency of NCF-1", "chronic granulomatous disease caused by mutation in NCF1", "autosomal recessive chronic granulomatous disease cytochrome b-positive type I", "Autosomal Recessive Cytochrome B-Positive Chronic Granulomatous Disease Type I", "granulomatous disease, chronic, autosomal recessive, cytochrome b-POSITIVE, type I", "granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 1", "Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I", "GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 1", "shortest_name_length": 4}
{"curie": "MONDO:0100069", "names": ["HIIMS", "hearing impairment and infertile male syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing impairment and infertile male syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0856139", "names": ["Aggravated Granuloma Annulare", "Granuloma annulare aggravated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Granuloma annulare aggravated", "shortest_name_length": 29}
{"curie": "UMLS:C1335347", "names": ["Parasite-Related Cancer", "Parasite-Related Malignancy", "Parasite-Related Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parasite-Related Malignant Neoplasm", "shortest_name_length": 23}
{"curie": "MONDO:0025598", "names": ["chlamydia pneumonia", "Chlamydia pneumonia", "chlamydial pneumonia", "Chlamydial pneumonia", "Chlamydia; pneumonia", "Pneumonia chlamydial", "Chlamydial Pneumonia", "pneumonia chlamydial", "Pneumonia, Chlamydial", "pneumonia; chlamydial", "Chlamydial Pneumonias", "Pneumonias, Chlamydial", "Chlamydophila Pneumonia", "Pneumonia, Chlamydophila", "Chlamydophila Pneumonias", "Pneumonias, Chlamydophila", "Chlamydia caused pneumonia", "Pneumonia due to chlamydia", "pneumonia caused by chlamydia", "bacterial pneumonia Chlamydial", "Chlamydia pneumoniae pneumonia", "Chlamydial pneumonia (diagnosis)", "Pneumonia caused by Chlamydiaceae", "Pneumonia caused by Chlamydiaceae (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pneumonia caused by chlamydia", "shortest_name_length": 19}
{"curie": "MONDO:0019982", "names": ["MRD", "PUJO", "bilateral MCDK", "Pelvi-ureteric junction obstruction", "bilateral multicystic renal dysplasia", "bilateral multicystic dysplastic kidney"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bilateral multicystic dysplastic kidney", "shortest_name_length": 3}
{"curie": "MONDO:0017929", "names": ["congenital achiasma", "Congenital achiasma", "Congenital absence of optic chiasma", "Congenital absence of optic chiasma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital achiasma", "shortest_name_length": 19}
{"curie": "MONDO:0010270", "names": ["MRXS7", "Mrxs7", "mental retardation X-linked syndromic 7", "Mental retardation X-linked syndromic 7", "mental retardation, X-linked syndromic 7", "MENTAL RETARDATION, X-LINKED, SYNDROMIC 7", "mental retardation, X-linked, syndromic 7", "Mental Retardation, X-Linked, Syndromic 7", "Ahmad X-linked mental retardation syndrome", "AHMAD X-LINKED MENTAL RETARDATION SYNDROME", "Ahmad X-linked Mental retardation syndrome", "X-linked intellectual disability Ahmad type", "Syndromic X-linked intellectual disability 7", "intellectual disability X-linked syndromic 7", "X-linked intellectual disability, Ahmad type", "syndromic X-linked intellectual disability 7", "intellectual disability, X-linked syndromic 7", "intellectual disability, X-linked, syndromic 7", "Ahmad X-linked intellectual disability syndrome", "syndromic X-linked intellectual disability type 7", "x-linked intellectual disability syndromic type 7", "Syndromic X-linked intellectual disability type 7", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 7", "Syndromic X-linked intellectual disability type 7 (disorder)", "Syndromic X-linked intellectual disability type 7 (diagnosis)", "mental retardation, obesity, hypogonadism, and tapering fingers", "intellectual disability, obesity, hypogonadism, and tapering fingers"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic X-linked intellectual disability 7", "shortest_name_length": 5}
{"curie": "MONDO:0019219", "names": ["disorder of neurotransmitter metabolism and transport", "inborn disorder of neurotransmitter metabolism and transport"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of neurotransmitter metabolism and transport", "shortest_name_length": 53}
{"curie": "MONDO:0019906", "names": ["r11", "RC11", "Ring 11", "r(11) syndrome", "chromosome 11 ring", "ring chromosome 11", "Ring chromosome 11", "Ring chromosome type 11", "Ring chromosome 11 syndrome", "Ring chromosome 11 syndrome (disorder)", "Ring chromosome 11 syndrome (diagnosis)", "anomaly of chromosome pair ring chromosome 11 syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ring chromosome 11", "shortest_name_length": 3}
{"curie": "UMLS:C3495814", "names": ["Fulminant type 1 diabetes mellitus", "Fulminant type I diabetes mellitus", "Fulminant type 1 diabetes mellitus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fulminant type 1 diabetes mellitus", "shortest_name_length": 34}
{"curie": "UMLS:C1140710", "names": ["Cerebral cavernous hemangioma", "Cerebral Cavernous Hemangioma", "Cerebral Cavernous Hemangiomas", "Cerebral cavernous haemangioma", "Cavernous Hemangioma, Cerebral", "Hemangioma, Cerebral Cavernous", "Cavernous Hemangiomas, Cerebral", "Hemangiomas, Cerebral Cavernous"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebral Cavernous Hemangioma", "shortest_name_length": 29}
{"curie": "UMLS:C2733483", "names": ["STARI", "Masters Disease", "Masters disease", "Southern Tick-Associated Rash Illness", "Southern tick-associated rash illness", "STARI Southern tick-associated rash illness", "STARI - Southern tick-associated rash illness", "Southern tick-associated rash illness (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Southern tick-associated rash illness", "shortest_name_length": 5}
{"curie": "MONDO:0032826", "names": ["NPHS21", "nephrotic syndrome type 21", "NEPHROTIC SYNDROME, TYPE 21", "nephrotic syndrome, type 21"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrotic syndrome, type 21", "shortest_name_length": 6}
{"curie": "UMLS:C0035354", "names": ["Axon Reaction", "axon reaction", "Axon Reactions", "Reaction, Axon", "Axonal Reaction", "Reactions, Axon", "Reaction, Axonal", "Axonal Reactions", "Reactions, Axonal", "Nissl degeneration", "Nissl Degeneration", "Degeneration, Nissl", "Retrograde Degeneration", "Retrograde Degenerations", "Degeneration, Retrograde", "Degenerations, Retrograde", "Nissl degeneration (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retrograde Degeneration", "shortest_name_length": 13}
{"curie": "MONDO:0025483", "names": ["mammary tumor", "mammary tumors", "Mammary Neoplasm", "mammary neoplasm", "Neoplasm, Mammary", "neoplasm, mammary", "mammary neoplasms", "Mammary Neoplasms", "Neoplasms, Mammary", "neoplasms, mammary", "animal mammary neoplasm", "Animal Mammary Neoplasm", "Neoplasm, Animal Mammary", "neoplasm, animal mammary", "Mammary Neoplasm, Animal", "Animal Mammary Neoplasms", "animal mammary neoplasms", "animal mammary carcinoma", "mammary neoplasm, animal", "animal mammary carcinomas", "Mammary Neoplasms, Animal", "mammary carcinoma, animal", "Neoplasms, Animal Mammary", "mammary neoplasms, animal", "carcinoma, animal mammary", "neoplasms, animal mammary", "mammary carcinomas, animal", "carcinomas, animal mammary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mammary neoplasms, animal", "shortest_name_length": 13}
{"curie": "MONDO:0004050", "names": ["TEOS", "Malignant Bone Aneurysm", "malignant bone aneurysm", "Telangiectatic Osteosarcoma", "Telangiectatic osteosarcoma", "telangiectatic osteosarcoma", "osteosarcoma; telangiectatic", "telangiectatic; osteosarcoma", "osteosarcoma, telangiectatic", "Telangiectatic Osteogenic Sarcoma", "telangiectatic osteogenic sarcoma", "sarcoma, osteogenic telangiectatic", "osteogenic sarcoma, telangiectatic", "Telangiectatic osteosarcoma (morphologic abnormality)", "telangiectatic osteosarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "telangiectatic osteogenic sarcoma", "shortest_name_length": 4}
{"curie": "MONDO:0018676", "names": ["EAF", "eosinophilic angiocentric fibrosis", "Sinonasal eosinophilic angiocentric fibrosis", "IgG4-related eosinophilic angiocentric fibrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eosinophilic angiocentric fibrosis", "shortest_name_length": 3}
{"curie": "MONDO:0014021", "names": ["FEPS1", "familial episodic pain syndrome 1", "episodic pain syndrome, familial, 1", "EPISODIC PAIN SYNDROME, FAMILIAL, 1", "episodic pain syndrome, familial, type 1", "familial episodic pain syndrome with predominantly upper body involvement", "Familial episodic pain syndrome with predominantly upper body involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial episodic pain syndrome with predominantly upper body involvement", "shortest_name_length": 5}
{"curie": "UMLS:C0003960", "names": ["aschoff body", "Aschoff Body", "Aschoff body", "Aschoff nodule", "aschoff bodies", "Aschoff Bodies", "Bodies, Aschoff", "Aschoff; bodies", "bodies; Aschoff", "Rheumatic nodule", "Aschoff's bodies", "Rheumatic Nodule", "aschoffs nodules", "rheumatic nodule", "Rheumatic Nodules", "Nodule, Rheumatic", "rheumatic nodules", "Nodules, Rheumatic", "Rheumatic nodule (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aschoff Bodies", "shortest_name_length": 12}
{"curie": "MONDO:0037745", "names": ["myxofibroma", "fibromyxoma", "Fibromyxoma", "Myxofibroma", "Fibromyxomas", "Myxofibromas", "Myxoid fibroma", "Myxofibroma, NOS", "Fibromyxoid Tumor", "fibromyxoid tumor", "fibromyxoma, benign", "FIBROMYXOMA, BENIGN", "Fibromyxoid Neoplasm", "fibromyxoid neoplasm", "Fibromyxoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibromyxoid tumor", "shortest_name_length": 11}
{"curie": "UMLS:C4331341", "names": ["Stage IVB Hypopharyngeal Throat Cancer", "Stage IVB Hypopharyngeal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Hypopharyngeal Carcinoma AJCC v8", "shortest_name_length": 38}
{"curie": "MONDO:0030831", "names": ["gastrointestinal defect and immunodeficiency syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastrointestinal defect and immunodeficiency syndrome", "shortest_name_length": 53}
{"curie": "MONDO:0017689", "names": ["Fructose disorder, NOS", "fructose; metabolic disorder", "metabolic disorder; fructose", "Fructose metabolism disorder", "Disorder of fructose metabolism", "disorder of fructose metabolism", "Disorders of fructose metabolism", "Fructose metabolism disorder (disorder)", "Fructose metabolism disorder (diagnosis)", "Disorder of fructose metabolism, unspecified", "carbohydrate transport and metabolism disorder fructose"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of fructose metabolism", "shortest_name_length": 22}
{"curie": "UMLS:C0853348", "names": ["Arthropod bite", "arthropod bite", "arthropod bites", "arthropod; bite", "bite; arthropod"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arthropod bite", "shortest_name_length": 14}
{"curie": "MONDO:0005880", "names": ["Esophagostomosis", "esophagostomiasis", "Oesophagostomosis", "Esophagostomiasis", "oesophagostomiasis", "Oesophagostomiases", "Oesophagostomiasis", "Nodular worm disease", "infection by Oesophagostomum", "Infection by Oesophagostomum", "Oesophagostomum infectious disease", "Oesophagostomum disease or disorder", "Infection by Oesophagostomum (disorder)", "Infection by Oesophagostomum (diagnosis)", "Oesophagostomum caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oesophagostomiasis", "shortest_name_length": 16}
{"curie": "MONDO:0001797", "names": ["Chancroid", "CHANCROID", "chancroid", "Chancroids", "ulcus molle", "Ulcus molle", "molle; ulcer", "Soft chancre", "ulcer; molle", "soft chancre", "CHANCRE, SOFT", "virulent; bubo", "bubo; virulent", "Simple chancre", "chancroid; bubo", "Ducrey's disease", "Bacillus; Ducrey", "Chancroidal bubo", "Ducrey's chancre", "Bubo chancroidal", "bubo; chancroidal", "Ulcus molle, skin", "chancroidal; bubo", "bubo; soft chancre", "Hemophilus ducreyi", "Ulcus molle, cutis", "Haemophilus ducreyi", "Chancroid (disorder)", "Soft sore - chancroid", "chancroid (diagnosis)", "Soft chancre - chancroid", "bubo; Hemophilus ducreyi", "bubo; Haemophilus ducreyi", "Hemophilus ducreyi infection", "Hemophilus ducreyi chancroid", "Ducrey's simple soft chancre", "Haemophilus ducreyi chancroid", "Haemophilus ducreyi infection", "Bubo due to Hemophilus ducreyi", "Bubo due to Haemophilus ducreyi", "sexually transmitted disease chancroid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chancroid", "shortest_name_length": 9}
{"curie": "MONDO:0100102", "names": ["FADS2", "FETAL AKINESIA DEFORMATION SEQUENCE 2", "fetal akinesia deformation sequence 2", "fetal akinesia deformation sequence syndrome 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fetal akinesia deformation sequence 2", "shortest_name_length": 5}
{"curie": "UMLS:C0751001", "names": ["basilar artery aneurysm", "aneurysm artery basilar", "Basilar Artery Aneurysm", "Basilar artery aneurysm", "Artery Aneurysm, Basilar", "Aneurysm, Basilar Artery", "Basilar Artery Aneurysms", "Aneurysms, Basilar Artery", "Artery Aneurysms, Basilar", "Aneurysm of basilar artery", "aneurysm of basilar artery", "Aneurysm of basilar artery (disorder)", "aneurysm of basilar artery (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aneurysm, Basilar Artery", "shortest_name_length": 23}
{"curie": "UMLS:C4054400", "names": ["Nephrotic Syndrome - ADCK4 Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - ADCK4 Associated", "shortest_name_length": 37}
{"curie": "MONDO:0014366", "names": ["SPGF14", "ZMYND15 azoospermia", "SPERMATOGENIC FAILURE 14", "spermatogenic failure 14", "spermatogenic failure type 14", "azoospermia caused by mutation in ZMYND15"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 14", "shortest_name_length": 6}
{"curie": "MONDO:0043330", "names": ["Mirizzi Syndrome", "Mirizzi syndrome", "mirizzi syndrome", "Syndrome, Mirizzi", "syndrome, Mirizzi", "Mirizzis syndrome", "Mirizzis Syndrome", "Mirizzi's Syndrome", "mirizzi's syndrome", "Mirizzi's syndrome", "Syndrome, Mirizzi's", "syndrome, Mirizzi's", "Mirizzi syndrome (diagnosis)", "Mirizzi's syndrome (disorder)", "hepatic duct dystonia syndrome", "Hepatic duct dystonia syndrome", "Extrinsic biliary compression syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mirizzi syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0008755", "names": ["Moynahan syndrome", "Moynahan's syndrome", "Moynahan alopecia syndrome", "MOYNAHAN ALOPECIA SYNDROME", "Moynahan's syndrome (diagnosis)", "alopecia-epilepsy-oligophrenia syndrome", "Progressive cardiomyopathic lentiginosis", "Alopecia epilepsy oligophrenia syndrome of Moynahan", "alopecia-epilepsy-oligophrenia syndrome of Moynahan", "alopecia epilepsy oligophrenia syndrome of Moynahan", "ALOPECIA-EPILEPSY-OLIGOPHRENIA SYNDROME OF MOYNAHAN", "Alopecia-Epilepsy-Oligophrenia Syndrome Of Moynahan", "alopecia-mental retardation-epilepsy-microcephaly syndrome", "microcephaly-sparse hair-mental retardation-seizures syndrome", "alopecia-epilepsy-intellectual disability syndrome, Moynahan type", "Alopecia-epilepsy-intellectual disability syndrome, Moynahan type", "Alopecia, epilepsy, intellectual disability syndrome Moynahan type", "Alopecia, epilepsy, intellectual disability syndrome Moynahan type (disorder)", "familial congenital alopecia-epilepsy-mental retardation-unusual EEG syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Moynahan syndrome", "shortest_name_length": 17}
{"curie": "MONDO:0007679", "names": ["GMS syndrome", "GMS SYNDROME", "GMS Syndrome", "Goniodysgenesis with mental deficiency and short stature", "Goniodysgenesis-Mental Retardation-Short Stature Syndrome", "GONIODYSGENESIS--MENTAL RETARDATION--SHORT STATURE SYNDROME", "Goniodysgenesis--mental retardation--short stature syndrome", "Goniodysgenesis-intellectual disability-short stature syndrome", "Goniodysgenesis--intellectual disability--short stature syndrome", "Goniodysgenesis with intellectual disability and short stature syndrome", "Goniodysgenesis with intellectual disability and short stature syndrome (disorder)", "Goniodysgenesis with intellectual disability and short stature syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "GMS syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0013648", "names": ["MUH", "Fph", "FPH", "FPHH", "FPH1", "FPH2, FORMERLY", "universal melanosis", "Universal melanosis", "melanosis diffusa congenita", "Melanosis diffusa congenita", "MELANOSIS UNIVERSALIS HEREDITARIA", "Melanosis universalis hereditaria", "melanosis universalis hereditaria", "Melanosis Universalis Hereditaria", "Familial progressive hyperpigmentation", "familial progressive hyperpigmentation", "HYPERPIGMENTATION, FAMILIAL PROGRESSIVE", "Hyperpigmentation, Familial Progressive", "HYPERPIGMENTATION, FAMILIAL PROGRESSIVE, 1", "hyperpigmentation, familial progressive, 1", "Familial progressive hyperpigmentation (disorder)", "HYPERPIGMENTATION, FAMILIAL PROGRESSIVE, 2, FORMERLY", "HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial progressive hyperpigmentation", "shortest_name_length": 3}
{"curie": "MONDO:0000598", "names": ["Alogia", "alogia", "Anepia", "Anepias", "Aphasia", "Alogias", "aphasia", "APHASIA", "APHASIAS", "Logagnosia", "Logamnesia", "Logamnesias", "Logasthenia", "Logagnosias", "Logasthenias", "Losing words", "Aphasia, NOS", "Word Deafness", "Loss of words", "Deafness, Word", "Aphasia syndrome", "Aphasia (finding)", "Aphasia Syndromes", "Aphasic disturbance", "Aphasic disturbance, NOS", "Difficulty finding words", "inability to understand or express language", "Loss of power of expression or comprehension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aphasia", "shortest_name_length": 6}
{"curie": "UMLS:C2062969", "names": ["mediastinal hemangioma", "Mediastinal Hemangioma", "hemangioma of mediastinum", "hemangioma of mediastinum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemangioma of mediastinum", "shortest_name_length": 22}
{"curie": "MONDO:0000955", "names": ["ileum cancer", "ileal neoplasm", "cancer of ileum", "Malignant tumor of ileum", "malignant ileal neoplasm", "malignant tumor of ileum", "malignant ileum neoplasm", "Malignant ileal neoplasm", "Malignant tumour of ileum", "malignant neoplasm of ileum", "Malignant neoplasm of ileum", "Malignant ileal neoplasm NOS", "Malignant neoplasm of ileum NOS", "Malignant tumor of ileum (disorder)", "malignant neoplasm of ileum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ileum cancer", "shortest_name_length": 12}
{"curie": "MONDO:0007064", "names": ["ADA", "SCID1", "ADA-SCID", "ADA deficiency", "ada deficiency", "ADA Deficiency", "ADA deficiency NOS", "Bubble boy disease", "Partial ADA Deficiency", "PARTIAL ADA DEFICIENCY", "partial ADA deficiency", "ADA deficiency with SCID", "SCID DUE TO ADA DEFICIENCY", "SCID due to ADA deficiency", "SCID Due to ADA Deficiency", "Swiss type agammaglobulinemia", "Swiss-type agammaglobulinemia", "Adenosine Deaminase Deficiency", "adenosine deaminase deficiency", "Swiss type; agammaglobulinemia", "Agammaglobulinemia, Swiss type", "AGAMMAGLOBULINEMIA, SWISS TYPE", "Adenosine deaminase deficiency", "agammaglobulinemia; Swiss type", "Agammaglobulinemia - Swiss type", "deficiency; adenosine deaminase", "adenosine deaminase; deficiency", "Agammaglobulinaemia - Swiss type", "Deficiency of adenosine deaminase", "Adenosine aminohydrolase deficiency", "Adenosine deaminase [ADA] deficiency", "SCID due to ADA deficiency, late-onset", "SCID due to absent lymphoid stem cells", "Partial adenosine deaminase deficiency", "SCID DUE TO ADA DEFICIENCY, LATE-ONSET", "SCID Due to ADA Deficiency, Late-Onset", "SCID DUE TO ADA DEFICIENCY, EARLY-ONSET", "SCID due to ADA deficiency, early-onset", "adenosine deaminase deficiency, partial", "Adenosine Deaminase Deficiency, Partial", "ADENOSINE DEAMINASE DEFICIENCY, PARTIAL", "SCID Due to ADA Deficiency, Early-Onset", "Adenosine deaminase deficiency (disorder)", "SCID Due to ADA Deficiency, Delayed Onset", "ADA - Adenosine aminohydrolase deficiency", "SCID DUE TO ADA DEFICIENCY, DELAYED ONSET", "SCID due to ADA deficiency, delayed onset", "Swiss-type agammaglobulinemia (diagnosis)", "adenosine deaminase deficiency (diagnosis)", "SCID due to adenosine deaminase deficiency", "Adenosine deaminase deficiency, unspecified", "Delayed-Late-Onset Adenosine Deaminase Deficiency", "Adenosine Deaminase Severe Combined Immunodeficiency", "Adenosine Deaminase Severe Combined Immune Deficiency", "Severe combined immunodeficiency, alymphocytotic type", "severe combined immunodeficiency due to ADA deficiency", "adenosine deaminase deficient severe combined immunodeficiency", "Adenosine Deaminase Deficient Severe Combined Immunodeficiency", "severe combined immunodeficiency due to absent lymphoid stem cells", "Severe combined immunodeficiency due to absent lymphoid stem cells", "severe combined immunodeficiency due to adenosine deaminase deficiency", "Adenosine deaminase-deficient severe combined immunodeficiency disease", "Severe combined immunodeficiency due to adenosine deaminase deficiency", "Severe combined immunodeficiency (SCID) due to absent lymphoid stem cells", "Adenosine deaminase [ADA] deficiency with severe combined immunodeficiency", "Severe combined immunodeficiency due to absent lymphoid stem cells (disorder)", "severe combined immunodeficiency due to absent lymphoid stem cells (diagnosis)", "adenosine deaminase deficiency, partial, Autosomal recessive, Somatic mosaicism", "severe combined immunodeficiency due to ADA deficiency, Autosomal recessive, Somatic mosaicism", "SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY", "Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due To Adenosine Deaminase Deficiency", "severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency", "shortest_name_length": 3}
{"curie": "MONDO:0001313", "names": ["Acute allergic serous otitis media", "acute allergic serous otitis media", "Acute allergic serous otitis media (disorder)", "acute allergic serous otitis media (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute allergic serous otitis media", "shortest_name_length": 34}
{"curie": "UMLS:C0027854", "names": ["neural manifestation", "Neurologic Manifestation", "neurologic manifestation", "Manifestation, Neurologic", "Neurologic Manifestations", "neurologic manifestations", "Manifestations, Neurologic", "neurological manifestation", "Neurological Manifestation", "neurological manifestations", "Neurological Manifestations", "manifestations neurological", "Manifestation, Neurological", "Manifestations, Neurological", "Neurologic Signs and Symptoms", "Neurologic manifestations of general diseases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neurologic Manifestations", "shortest_name_length": 20}
{"curie": "MONDO:0011387", "names": ["PSORS4", "psoriasis 4", "psoriasis susceptibility 4", "psoriasis 4, susceptibility to", "PSORIASIS 4, SUSCEPTIBILITY TO", "PSORIASIS SUSCEPTIBILITY 4 (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "psoriasis 4, susceptibility to", "shortest_name_length": 6}
{"curie": "UMLS:C5556771", "names": ["Recurrent T-Cell Large Granular Lymphocyte Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent T-Cell Large Granular Lymphocyte Leukemia", "shortest_name_length": 51}
{"curie": "UMLS:C1335996", "names": ["Small Intestinal GIST", "Small Intestine Digestive Stromal Tumor", "Digestive Stromal Tumor of Small Intestine", "Small Intestine Digestive Stromal Neoplasm", "Digestive Stromal Neoplasm of Small Intestine", "Digestive Stromal Tumor of the Small Intestine", "Small Intestinal Gastrointestinal Stromal Tumor", "Gastrointestinal Stromal Tumor of Small Intestine", "Digestive Stromal Neoplasm of the Small Intestine", "Small Intestine Gastrointestinal Stromal Neoplasm", "Gastrointestinal stromal tumor of small intestine", "Gastrointestinal stromal tumour of small intestine", "Gastrointestinal Stromal Neoplasm of Small Intestine", "Gastrointestinal Stromal Tumor of the Small Intestine", "Small Intestinal Gastrointestinal Stromal Tumor (GIST)", "Gastrointestinal Stromal Neoplasm of the Small Intestine", "Gastrointestinal stromal tumor of small intestine (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal stromal tumor of small intestine", "shortest_name_length": 21}
{"curie": "UMLS:C1261566", "names": ["larynx; absent", "agenesis; larynx", "larynx; agenesis", "Agenesis of larynx", "Laryngeal Agenesis", "agenesis of larynx", "Agenesis of Larynx", "Congenital laryngeal atresia", "absence; larynx (congenital)", "Congenital absence of larynx", "Agenesis of larynx (disorder)", "Absence or agenesis of larynx", "agenesis of larynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Agenesis of larynx", "shortest_name_length": 14}
{"curie": "MONDO:0023575", "names": ["Krauss Herman Holmes syndrome", "Telecanthus-hypertelorism-strabismus-pes cavus syndrome", "Telecanthus, hypertelorism, strabismus, pes cavus syndrome", "telecanthus, hypertelorism, strabismus, and pes cavus syndrome", "Telecanthus, hypertelorism, strabismus, and pes cavus syndrome", "Telecanthus, hypertelorism, strabismus, pes cavus syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Krauss Herman Holmes syndrome", "shortest_name_length": 29}
{"curie": "MONDO:0010856", "names": ["PKDTS", "TSC2/PKD1 contiguous gene syndrome", "TSC2-PKD1 Contiguous Gene Deletion Syndrome", "CHROMOSOME 16p13.3 DELETION SYNDROME, DISTAL", "chromosome 16P13.3 deletion syndrome, distal", "polycystic kidneys, severe infantile with tuberous sclerosis", "Polycystic kidneys, severe infantile with tuberous sclerosis", "Polycystic Kidney Disease, Infantile Severe, With Tuberous Sclerosis", "polycystic kidney disease, infantile severe, with tuberous sclerosis", "Polycystic Kidney Disease, Infantile Severe, with Tuberous Sclerosis", "POLYCYSTIC KIDNEY DISEASE, INFANTILE SEVERE, WITH TUBEROUS SCLEROSIS", "tuberous sclerosis/polycystic kidney disease contiguous gene syndrome", "Tuberous sclerosis-polycystic kidney disease contiguous gene syndrome", "TUBEROUS SCLEROSIS/POLYCYSTIC KIDNEY DISEASE CONTIGUOUS GENE SYNDROME", "tuberous sclerosis polycystic kidney disease contiguous gene syndrome", "Tuberous sclerosis/polycystic kidney disease contiguous gene syndrome", "Tuberous sclerosis, polycystic kidney disease contiguous gene syndrome", "autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis", "Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis", "Autosomal Dominant Polycystic Kidney Disease Type 1 with Tuberous Sclerosis", "Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis", "shortest_name_length": 5}
{"curie": "MONDO:0013201", "names": ["WS4B", "EDN3 Waardenburg syndrome", "Waardenburg syndrome type 4B", "WAARDENBURG SYNDROME, TYPE 4B", "Waardenburg syndrome, type 4B", "Waardenburg Syndrome, Type 4b", "Waardenburg syndrome type IVB", "Waardenburg Syndrome, Type Ivb", "WAARDENBURG SYNDROME, TYPE IVB", "Waardenburg syndrome caused by mutation in EDN3", "Waardenburg syndrome with Hirschsprung disease type 4B", "WAARDENBURG SYNDROME, TYPE 4B, WITH HIRSCHSPRUNG DISEASE", "Waardenburg Syndrome, Type 4b, With Hirschsprung Disease", "Waardenburg syndrome, type 4B, with Hirschsprung disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Waardenburg syndrome type 4B", "shortest_name_length": 4}
{"curie": "UMLS:C1335122", "names": ["Mouth Mucosal Melanoma", "Mucosal Melanoma of Mouth", "Oral Cavity Mucosal Melanoma", "Mucosal Melanoma of the Mouth", "Mucosal Melanoma of Oral Cavity", "Mucosal Melanoma of the Oral Cavity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral Cavity Mucosal Melanoma", "shortest_name_length": 22}
{"curie": "UMLS:C1698677", "names": ["Intraoperative urinary injury", "intraoperative urinary injury", "Intraoperative Urinary System Injury", "intraoperative urinary injury (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraoperative Urinary System Injury", "shortest_name_length": 29}
{"curie": "MONDO:0005591", "names": ["pit and fissure surface dental caries"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pit and fissure surface dental caries", "shortest_name_length": 37}
{"curie": "UMLS:C4288935", "names": ["Hypomorphic Rag1 deficiency", "Hypomorphic RAG1 Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypomorphic RAG1 Deficiency", "shortest_name_length": 27}
{"curie": "UMLS:C1880779", "names": ["First trimester bleeding", "first trimester bleeding", "First Trimester Bleeding", "first trimester bleeding (symptom)", "First trimester bleeding (disorder)", "bleeding during the first trimester of pregnancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "First trimester bleeding", "shortest_name_length": 24}
{"curie": "MONDO:0012552", "names": ["MEN4", "MEN 4", "Multiple endocrine neoplasia type 4", "Multiple Endocrine Neoplasia Type 4", "multiple endocrine neoplasia type 4", "CDKN1B multiple endocrine neoplasia", "multiple endocrine neoplasia, type 4", "Type IV multiple endocrine neoplasia", "MULTIPLE ENDOCRINE NEOPLASIA, TYPE IV", "Multiple Endocrine Neoplasia, Type IV", "multiple endocrine neoplasia, type IV", "MEN (multiple endocrine neoplasia) 4 syndrome", "Multiple endocrine neoplasia type 4 (disorder)", "multiple endocrine neoplasia, type IV (diagnosis)", "Multiple Endocrine Neoplasia Type 1-Like Syndrome", "multiple endocrine neoplasia caused by mutation in CDKN1B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple endocrine neoplasia type 4", "shortest_name_length": 4}
{"curie": "UMLS:C4526734", "names": ["Lung Squamous Cell Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Squamous Cell Carcinoma by AJCC v7 Stage", "shortest_name_length": 45}
{"curie": "UMLS:C3888706", "names": ["Medical device site erosion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Medical device site erosion", "shortest_name_length": 27}
{"curie": "MONDO:0015030", "names": ["sclerosing perineurioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sclerosing perineurioma", "shortest_name_length": 23}
{"curie": "UMLS:C0852628", "names": ["Arterial embolism limb", "artery; embolism, limb", "Embolism arterial (limb)", "embolism; arterial, limb", "Arterial embolism (limbs)", "embolism; arterial, limb, arterial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arterial embolism (limbs)", "shortest_name_length": 22}
{"curie": "UMLS:C4763864", "names": ["Chronic Kidney Disease due to Diabetes Mellitus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic Kidney Disease due to Diabetes Mellitus", "shortest_name_length": 47}
{"curie": "UMLS:C2987415", "names": ["Gastric Adenoma, Gastric-Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Adenoma, Gastric-Type", "shortest_name_length": 29}
{"curie": "MONDO:0002218", "names": ["temporal lobe cancer", "tumor of Temporal Lobe", "temporal lobe neoplasm", "cancer of temporal lobe", "neoplasm of temporal lobe", "malignant temporal lobe neoplasm", "malignant neoplasm of temporal lobe", "Malignant neoplasm of temporal lobe", "Malignant neoplasm of temporal lobe (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "temporal lobe cancer", "shortest_name_length": 20}
{"curie": "MONDO:0016160", "names": ["X-linked intellectual disability-epilepsy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability-epilepsy syndrome", "shortest_name_length": 50}
{"curie": "UMLS:C0041648", "names": ["uncinariasis", "Uncinariasis", "UNCINARIASIS", "Uncinariosis", "Infection by Uncinaria", "Infection by Uncinaria, NOS", "Infection caused by Uncinaria", "Hookworm infection by Uncinaria", "Infection caused by Uncinaria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infection by Uncinaria", "shortest_name_length": 12}
{"curie": "MONDO:0017147", "names": ["PAH", "PHT", "IPAH", "Primary pulmonary hypertension", "Primary Pulmonary Hypertension", "Hypertension, Primary Pulmonary", "Pulmonary Hypertension, Primary", "PULMONARY ARTERIAL HYPERTENSION", "Idiopathic Pulmonary Hypertension", "Pulmonary Hypertension, Idiopathic", "Hypertension, Idiopathic Pulmonary", "Primary pulmonary arterial hypertension", "primary pulmonary arterial hypertension", "Idiopathic pulmonary arterial hypertension", "idiopathic pulmonary arterial hypertension", "Idiopathic Pulmonary Arterial Hypertension", "Idiopathic pulmonary arterial hypertension (disorder)", "idiopathic pulmonary arterial hypertension (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic pulmonary arterial hypertension", "shortest_name_length": 3}
{"curie": "MONDO:0012584", "names": ["SLEB9", "CR2 systemic lupus erythematosus (disease)", "susceptibility to systemic lupus erythematosus 9", "SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 9", "systemic lupus erythematosus, susceptibility to, 9", "systemic lupus erythematosus, susceptibility to, type 9", "systemic lupus erythematosus (disease) caused by mutation in CR2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "systemic lupus erythematosus, susceptibility to, 9", "shortest_name_length": 5}
{"curie": "OMIM:612271", "names": ["SHEP11", "MELANESIAN BLOND HAIR", "SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 11", "Skin-Hair-Eye Pigmentation, Variation In, 11", "SKIN/HAIR/EYE PIGMENTATION 11, BLUE/NONBLUE EYES", "Skin-Hair-Eye Pigmentation 11, Blue-Nonblue Eyes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 6}
{"curie": "MONDO:0002553", "names": ["angle tumor", "Angle Tumor", "Tumor, Angle", "Angle Tumors", "Tumors, Angle", "C-P Angle Tumor", "C-P angle tumor", "tumor of C-P angle", "Tumor of C-P Angle", "C-P Angle Neoplasm", "C-P angle neoplasm", "neoplasm of C-P angle", "Neoplasm of C-P Angle", "Tumor of the C-P Angle", "tumor of the C-P angle", "neoplasm of the C-P angle", "Neoplasm of the C-P Angle", "Cerebellopontine angle tumor", "Cerebellopontine Angle Tumor", "cerebellopontine angle tumor", "Angle Tumor, Cerebellopontine", "Cerebellopontine angle tumour", "Cerebellopontine Angle Tumors", "cerebellopontine angle tumour", "cerebellopontine angle tumors", "Tumor, Cerebellopontine Angle", "angle cerebellopontine tumors", "Angle Tumors, Cerebellopontine", "cerebellar Pontine angle tumor", "Cerebellar Pontine Angle Tumor", "Tumors, Cerebellopontine Angle", "Tumor of Cerebellopontine Angle", "cerebellopontine angle neoplasm", "Cerebellopontine Angle Neoplasm", "tumor of cerebellopontine angle", "tumor of cerebellar Pontine angle", "cerebellar Pontine angle neoplasm", "Cerebellar Pontine Angle Neoplasm", "Tumor of Cerebellar Pontine Angle", "Neoplasm of Cerebellopontine Angle", "neoplasm of cerebellopontine angle", "Tumor of the Cerebellopontine Angle", "tumor of the cerebellopontine angle", "neoplasm of cerebellar Pontine angle", "Neoplasm of Cerebellar Pontine Angle", "Tumor of the Cerebellar Pontine Angle", "tumor of the cerebellar Pontine angle", "Neoplasm of the Cerebellopontine Angle", "neoplasm of the Cerebellopontine Angle", "neoplasm of the cerebellopontine angle", "Cerebellopontine angle tumor (disorder)", "neoplasm of the cerebellar Pontine angle", "Neoplasm of the Cerebellar Pontine Angle", "cerebellopontine angle neoplasm (disease)", "neoplasm of cerebellopontine angle (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellopontine angle tumor", "shortest_name_length": 11}
{"curie": "UMLS:C3899504", "names": ["Congenital Hypergonadotropic Hypogonadism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Hypergonadotropic Hypogonadism", "shortest_name_length": 41}
{"curie": "UMLS:C0861157", "names": ["Decreased night vision", "Decrease in night vision"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Decreased night vision", "shortest_name_length": 22}
{"curie": "UMLS:C4054397", "names": ["Nephrotic Syndrome - ARHGDIA Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - ARHGDIA Associated", "shortest_name_length": 39}
{"curie": "MONDO:0018481", "names": ["undifferentiated esophageal cancer", "Undifferentiated Esophageal Cancer", "esophagus undifferentiated carcinoma", "Esophageal Undifferentiated Carcinoma", "esophageal undifferentiated carcinoma", "Undifferentiated esophageal carcinoma", "undifferentiated esophageal carcinoma", "Undifferentiated oesophageal carcinoma", "undifferentiated carcinoma of esophagus", "Undifferentiated carcinoma of esophagus", "Undifferentiated carcinoma of oesophagus", "Undifferentiated carcinoma of esophagus (disorder)", "undifferentiated carcinoma of esophagus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "undifferentiated carcinoma of esophagus", "shortest_name_length": 34}
{"curie": "MONDO:0037255", "names": ["serous ovarian tumor", "Ovarian Serous Tumor", "ovarian serous tumor", "serous tumor of ovary", "Serous Tumor of Ovary", "Ovarian Serous Neoplasm", "ovarian serous neoplasm", "serous neoplasm of ovary", "Serous Neoplasm of Ovary", "serous tumor of the ovary", "Serous Tumor of the Ovary", "serous neoplasm of the ovary", "Serous Neoplasm of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian serous tumor", "shortest_name_length": 20}
{"curie": "MONDO:0007407", "names": ["MC", "Meltzer Syndrome", "MELTZER SYNDROME", "Meltzer syndrome", "mixed cryoglobulinemia", "Mixed cryoglobulinemia", "Primary cryoglobulinemia", "primary cryoglobulinemia", "Primary cryoglobulinaemia", "Cryoglobulinemia, primary", "Essential cryoglobulinemia", "essential cryoglobulinemia", "Cryoglobulinemic vasculitis", "cryoglobulinemic vasculitis", "vasculitis; cryoglobulinemic", "Cryoglobulinaemic vasculitis", "cryoglobulinemic; vasculitis", "familial mixed cryoglobulinemia", "cryoglobulinemia, familial mixed", "Essential mixed cryoglobulinemia", "Cryoglobulinemia, Familial Mixed", "mixed essential cryoglobulinemia", "cryoglobulinemia essential mixed", "CRYOGLOBULINEMIA, FAMILIAL MIXED", "essential mixed cryoglobulinemia", "Essential mixed cryoglobulinaemia", "Primary cryoglobulinemia (disorder)", "Essential cryoglobulinemic vasculitis", "Cryoglobulinemic vasculitis (disorder)", "Essential cryoglobulinaemic vasculitis", "cryoglobulinemic vasculitis (diagnosis)", "Essential mixed cryoglobulinemia (disorder)", "mixed essential cryoglobulinemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cryoglobulinemic vasculitis", "shortest_name_length": 2}
{"curie": "MONDO:0010841", "names": ["WS2B", "Waardenburg syndrome type 2B", "WAARDENBURG SYNDROME, TYPE 2B", "Waardenburg Syndrome, Type 2B", "Waardenburg syndrome, type 2B", "Waardenburg syndrome type IIB", "Waardenburg Syndrome, Type IIB", "WAARDENBURG SYNDROME, TYPE IIB", "WAARDENBURG SYNDROME, TYPE 2B (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Waardenburg syndrome type 2B", "shortest_name_length": 4}
{"curie": "MONDO:0005912", "names": ["PCP Abuse", "pcp abuse", "abuse pcp", "PCP abuse", "Abuse, PCP", "PCP; abuse", "abuse; PCP", "PCP ADDICTION", "DRUG ABUSE PCP", "Angel Dust Abuse", "Abuse, Angel Dust", "phencyclidine abuse", "Phencyclidine Abuse", "Phencyclidine abuse", "abuse; phencyclidine", "Abuse, Phencyclidine", "phencyclidine; abuse", "Phencyclidine Abuses", "DRUG ABUSE ANGEL DUST", "Phencyclidine (PCP) abuse", "Phencyclidine abuse (disorder)", "phencyclidine abuse (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phencyclidine abuse", "shortest_name_length": 9}
{"curie": "MONDO:0014003", "names": ["DEE15", "EIEE15", "early infantile epileptic encephalopathy 15", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 15", "developmental and epileptic encephalopathy 15", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 15", "epileptic encephalopathy, early infantile, 15", "developmental and epileptic encephalopathy, 15", "epileptic encephalopathy, early infantile, type 15"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 15", "shortest_name_length": 5}
{"curie": "MONDO:0100483", "names": ["TDR-TB", "totally drug-resistant tuberculosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "totally drug-resistant tuberculosis", "shortest_name_length": 6}
{"curie": "MONDO:0007744", "names": ["HALP1", "HDLCQ10", "Hdlcq10", "CETP deficiency", "CEPT deficiency", "CETP DEFICIENCY", "hyperalphalipoproteinemia", "hyperalphalipoproteinemia 1", "HYPERALPHALIPOPROTEINEMIA 1", "hyperalphalipoproteinemia type 1", "Familial hyperalphalipoproteinemia", "familial hyperalphalipoproteinemia", "Familial hyperalphalipoproteinaemia", "Cholesterol-ester transfer protein deficiency", "cholesterol-ester transfer protein deficiency", "CHOLESTEROL ESTER TRANSFER PROTEIN DEFICIENCY", "cholesterol ester transfer Protein deficiency", "Familial hyperalphalipoproteinemia (disorder)", "high density lipoprotein cholesterol level QTL 10", "high density lipoprotein cholesterol level quantitative trait locus 10", "HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholesterol-ester transfer protein deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C1335113", "names": ["Liver Fluke-Related Cholangiocarcinoma", "Opisthorchis Viverrini-Related Cholangiocarcinoma", "Opisthorchis Viverrini-Related Cholangiocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Opisthorchis Viverrini-Related Cholangiocarcinoma", "shortest_name_length": 38}
{"curie": "UMLS:C1336335", "names": ["Stage IVA Esophagus Adenocarcinoma", "Stage IVA Esophageal Adenocarcinoma", "Stage IVA Adenocarcinoma of Esophagus", "Stage IVA Adenocarcinoma of the Esophagus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Esophageal Adenocarcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0007041", "names": ["ACS1", "ACS 2", "ACS 1", "ACS I", "Apert", "ACS II", "Apert syndrome", "apert syndrome", "APERT SYNDROME", "Apert Syndrome", "Syndrome, Apert", "apert's syndrome", "Apert's syndrome", "VOGT CEPHALODACTYLY", "Vogt Cephalodactyly", "acrocephalosyndactyly", "Apert-Crouzon Disease", "Apert Crouzon Disease", "apert-Crouzon disease", "APERT-CROUZON DISEASE", "Acrocephalosyndactyly", "ACROCEPHALOSYNDACTYLY", "Syndactylic Oxycephaly", "Acrocephalosyndactylia", "Disease, Apert-Crouzon", "acrocephalosyndactylia", "syndactylic oxycephaly", "Acrocephalosyndactylias", "Acroencephalosyndactyly", "Syndactylic Oxycephalies", "acrocephalopolysyndactyly", "acrocephalosyndactyly type 1", "Acrocephalosyndactyly type I", "Type I Acrocephalosyndactyly", "type I Acrocephalosyndactyly", "Acrocephalosyndactyly type 1", "acrocephalosyndactyly type I", "Acrocephalosyndactyly Type I", "Acrocephalosyndactyly, Type 1", "acrocephalosyndactyly, type 2", "Acrocephalosyndactyly (Apert)", "Acrocephalosyndactyly [Apert]", "Type II Acrocephalosyndactyly", "Kurczynski Casperson Syndrome", "Acrocephalosyndactyly, type I", "acrocephalosyndactyly, type 1", "ACROCEPHALOSYNDACTYLY, TYPE I", "acrocephalo-syndactyly type 1", "Acrocephalosyndactyly, Type I", "Acrocephalosyndactyly, Type II", "Syndrome, Kurczynski Casperson", "Type I Acrocephalosyndactylies", "ACROCEPHALOSYNDACTYLY, TYPE II", "Acrocephalosyndactylies, Type 1", "Type II Acrocephalosyndactylies", "Acrocephalosyndactylies, Type I", "Acrocephalosyndactylies, Type II", "Acrocephalosyndactyly (disorder)", "acrocephalosyndactyly (diagnosis)", "Acrocephalosyndactyly syndrome, type I", "Acrocephalosyndactyly type I (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "apert syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0023002", "names": ["double discordia", "corrected transposition", "atrio-ventricular and ventriculo-arterial double Discordia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "double discordia", "shortest_name_length": 16}
{"curie": "UMLS:C0814154", "names": ["ARND", "FAE (Fetal Alcohol Effects)", "FAEs (Fetal Alcohol Effects)", "alcohol-related neurodevelopmental disorder", "Alcohol Related Neurodevelopmental Disorder", "Growth Retardation, Facial Abnormalities, and Central Nervous System Dysfunction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alcohol Related Neurodevelopmental Disorder", "shortest_name_length": 4}
{"curie": "MONDO:0004309", "names": ["Sarcomatosis", "sarcomatosis", "Sarcomatosis NOS", "Sarcomatosis, NOS", "Sarcomatosis (morphologic abnormality)", "sarcomatosis (morphologic abnormality)", "sarcomatosis NOS (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sarcomatosis", "shortest_name_length": 12}
{"curie": "UMLS:C1167686", "names": ["Nail toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nail toxicity", "shortest_name_length": 13}
{"curie": "MONDO:0020795", "names": ["SRS5", "SILVER-RUSSELL SYNDROME 5", "Silver-Russell syndrome 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Silver-Russell syndrome 5", "shortest_name_length": 4}
{"curie": "UMLS:C0521495", "names": ["Application site rash", "Administration site rash", "APPLICATION SITE DERMATITIS", "Application site dermatitis", "Application site rash (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Application site rash", "shortest_name_length": 21}
{"curie": "MONDO:0009024", "names": ["cortical blindness, retardation, and postaxial polydactyly", "Cortical Blindness, Retardation, and Postaxial Polydactyly", "CORTICAL BLINDNESS, RETARDATION, AND POSTAXIAL POLYDACTYLY", "cortical blindness-intellectual disability-polydactyly syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cortical blindness-intellectual disability-polydactyly syndrome", "shortest_name_length": 58}
{"curie": "MONDO:0013478", "names": ["FPLD4", "PLIN1-related FPLD", "FPLD due to PLIN1 mutations", "familial partial lipodystrophy type 4", "lipodystrophy, familial partial, type 4", "LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 4", "PLIN1-related familial partial lipodystrophy", "FPLD4 - familial partial lipodystrophy type 4", "Perilipin 1 related familial partial lipodystrophy", "Perilipin 1 related familial partial lipodystrophy (disorder)", "familial partial lipodystrophy associated with PLIN1 mutations", "lipodystrophy, familial partial, associated with Plin1 mutations", "LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PLIN1 MUTATIONS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PLIN1-related familial partial lipodystrophy", "shortest_name_length": 5}
{"curie": "UMLS:C1167765", "names": ["Wound infection staphylococcal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wound infection staphylococcal", "shortest_name_length": 30}
{"curie": "MONDO:0002619", "names": ["Bone Fibrosarcoma", "bone fibrosarcoma", "Fibrosarcoma of Bone", "fibrosarcoma of bone", "Fibrosarcoma of bone", "malignant histiocytosis", "malignant fibroxanthoma", "Fibrosarcoma of the Bone", "fibrosarcoma of the bone", "Fibrosarcoma of bone (disorder)", "fibrosarcoma of bone (diagnosis)", "bone tissue fibrosarcoma (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bone fibrosarcoma", "shortest_name_length": 17}
{"curie": "MONDO:0005334", "names": ["familial nephritis", "Familial nephritis", "Familial Nephritis", "Nephritis, Familial", "nephritis, familial", "hereditary nephritis", "Hereditary Nephritis", "Hereditary nephritis", "NEPHRITIS, HEREDITARY", "Nephritis, Hereditary", "Chronic hereditary nephritis", "Hereditary nephritis syndrome", "Hereditary glomerulonephritis", "hemorrhagic familial nephritis", "Hereditary nephritis (disorder)", "hereditary nephritis (diagnosis)", "GN - Hereditary glomerulonephritis", "Hereditary Interstitial Pyelonephritis", "Pyelonephritis, Hereditary Interstitial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary nephritis", "shortest_name_length": 18}
{"curie": "MONDO:0013011", "names": ["ASD5", "atrial septal defect 5", "ATRIAL SEPTAL DEFECT 5", "Atrial Septal Defect 5", "atrial septal defect type 5", "atrial heart septal defect 5", "atrial septal defect 5 - ASD5", "ACTC1 atrial heart septal defect", "atrial heart septal defect type 5", "atrial septal defect 5 - ASD5 (diagnosis)", "atrial heart septal defect caused by mutation in ACTC1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial septal defect 5", "shortest_name_length": 4}
{"curie": "MONDO:0008998", "names": ["Cockayne syndrome type C", "Cockayne syndrome type 3", "Cockayne syndrome type III", "Cockayne syndrome, type III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cockayne syndrome type 3", "shortest_name_length": 24}
{"curie": "MONDO:0003624", "names": ["acinar cell breast carcinoma", "acinic cell breast carcinoma", "Acinic Cell Breast Carcinoma", "Breast Acinic Cell Carcinoma", "breast carcinoma of acinar cell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acinic cell breast carcinoma", "shortest_name_length": 28}
{"curie": "UMLS:C1708648", "names": ["Laryngeal Acantholytic Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laryngeal Acantholytic Squamous Cell Carcinoma", "shortest_name_length": 46}
{"curie": "UMLS:C0751181", "names": ["Forehead Trauma", "forehead trauma", "injury; forehead", "Forehead Traumas", "Trauma, Forehead", "forehead; injury", "forehead injuries", "Traumas, Forehead", "Injury of forehead", "of forehead injury", "Frontal Region Trauma", "Trauma, Frontal Region", "facial injury forehead", "Region Trauma, Frontal", "Frontal Region Traumas", "injury; frontal region", "Region Traumas, Frontal", "Traumas, Frontal Region", "Injury of forehead (disorder)", "Injury of forehead (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Frontal Region Trauma", "shortest_name_length": 15}
{"curie": "MONDO:0008104", "names": ["NS1", "Noonan syndrome", "Noonan Syndrome 1", "NOONAN SYNDROME 1", "Noonan syndrome 1", "Male Turner syndrome", "MALE TURNER SYNDROME", "Male Turner Syndrome", "male turner syndrome", "male Turner syndrome", "male turners syndrome", "Turner Syndrome, Male", "Male Turner's Syndrome", "Noonan syndrome type 1", "males syndrome turners", "males syndrome turner's", "Turner's Syndrome, Male", "pterygium colli syndrome", "TURNER SYNDROME IN MALES", "Male Turner-like syndrome", "Female Pseudo Turner Syndrome", "Female Pseudo-Turner Syndrome", "female pseudo-Turner syndrome", "FEMALE PSEUDO-TURNER SYNDROME", "Pseudo-Turner Syndrome, Female", "Turner phenotype with normal karyotype"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Noonan syndrome 1", "shortest_name_length": 3}
{"curie": "MONDO:0017269", "names": ["X-linked ichthyosis syndrome", "X-linked inherited ichthyosis syndromic form", "inherited ichthyosis syndromic form, X-linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked ichthyosis syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0030911", "names": ["MRD46", "autosomal dominant mental retardation 46", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 46", "mental retardation, autosomal dominant 46", "autosomal dominant intellectual disability 46", "intellectual disability, autosomal dominant 46", "autosomal dominant intellectual developmental disorder 46", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 46"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 46", "shortest_name_length": 5}
{"curie": "UMLS:C1883030", "names": ["Signet Ring Melanoma", "Signet-Ring Melanoma", "Signet-Ring Skin Melanoma", "Signet Ring Skin Melanoma", "Signet Ring Cutaneous (Skin) Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Signet Ring Melanoma", "shortest_name_length": 20}
{"curie": "MONDO:0007210", "names": ["Brachmann-de Lange-like facial changes with microcephaly, metatarsus adductus, and developmental delay", "BRACHMANN-DE LANGE-LIKE FACIAL CHANGES WITH MICROCEPHALY, METATARSUS ADDUCTUS, AND DEVELOPMENTAL DELAY", "Brachmann-De Lange-Like Facial Changes With Microcephaly, Metatarsus Adductus, And Developmental Delay"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brachmann-de Lange-like facial changes with microcephaly, metatarsus adductus, and developmental delay", "shortest_name_length": 102}
{"curie": "MONDO:0002483", "names": ["Breast Myoepithelial Tumor", "breast myoepithelial tumor", "breast myoepithelial neoplasm", "Breast Myoepithelial Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast myoepithelial tumor", "shortest_name_length": 26}
{"curie": "MONDO:0003461", "names": ["fallopian tube adenofibroma", "Fallopian Tube Adenofibroma", "Fallopian Tube Serous Adenofibroma", "fallopian tube serous adenofibroma", "serous adenofibroma of fallopian tube"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fallopian tube serous adenofibroma", "shortest_name_length": 27}
{"curie": "MONDO:0013669", "names": ["BROVCA4", "RAD51D hereditary breast ovarian cancer syndrome", "susceptibility to familial breast-ovarian cancer 4", "BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 4", "breast-ovarian cancer, familial, susceptibility to, 4", "breast-ovarian cancer, familial, susceptibility to, type 4", "hereditary breast ovarian cancer syndrome caused by mutation in RAD51D"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast-ovarian cancer, familial, susceptibility to, 4", "shortest_name_length": 7}
{"curie": "MONDO:0021476", "names": ["benign tongue tumor", "Benign Tongue Tumor", "benign tongue tumors", "Benign Tongue Neoplasm", "benign tongue neoplasm", "tongue benign neoplasm", "Benign tongue neoplasm", "Benign tumor of tongue", "Tongue neoplasm benign", "benign neoplasm tongue", "benign tumor of tongue", "Benign Tumor of Tongue", "tongue neoplasm, benign", "Benign tumour of tongue", "Tongue Neoplasm, Benign", "benign neoplasm of tongue", "Benign neoplasm of tongue", "Benign Neoplasm of Tongue", "Benign Tumor of the Tongue", "benign tumor of the tongue", "Benign Neoplasm of the Tongue", "benign neoplasm of the tongue", "Benign neoplasm of tongue, NOS", "Benign neoplasm of tongue (disorder)", "benign neoplasm of tongue (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of tongue", "shortest_name_length": 19}
{"curie": "MONDO:0011076", "names": ["DRM", "IBM1", "MFM1", "desminopathy", "Desminopathy", "IBM1, FORMERLY", "ARVC7, FORMERLY", "CDCD3, FORMERLY", "ARVD7, FORMERLY", "LGMD2R, FORMERLY", "CMD1F and LGMD1D", "desminopathy, primary", "DESMINOPATHY, PRIMARY", "Desminopathy, Primary", "desmin-related myopathy", "myofibrillar myopathy 1", "Desmin-Related Myopathy", "DESMIN-RELATED MYOPATHY", "Myopathy, Desmin-Related", "myopathy, myofibrillar, 1", "MYOPATHY, MYOFIBRILLAR, 1", "CMD1F AND LGMD1D, FORMERLY", "CMD1F and LGMD1D, formerly", "myofibrillar myopathy type 1", "myopathy, myofibrillar, type 1", "DES myofibrillar myopathy (disease)", "Desmin-related myofibrillar myopathy", "desmin-related myofibrillar myopathy", "Myopathy, Myofibrillar, Desmin-Related", "MYOPATHY, MYOFIBRILLAR, DESMIN-RELATED", "myopathy, myofibrillar, desmin-related", "muscular dystrophy, limb-girdle type 2R", "inclusion body myopathy 1, autosomal dominant", "Desmin-related myofibrillar myopathy (disorder)", "arrhythmogenic right ventricular cardiomyopathy 7", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2R, FORMERLY", "muscular dystrophy, limb-girdle type 2R (diagnosis)", "progressive muscular dystrophy - limb girdle - type 2r", "DES autosomal recessive limb-girdle muscular dystrophy", "arrhythmogenic right ventricular dysplasia, familial, 7", "inclusion body myopathy 1, autosomal dominant, formerly", "INCLUSION BODY MYOPATHY 1, AUTOSOMAL DOMINANT, FORMERLY", "Mfm, Desmin-Related Myofibrillar Myopathy, Desmin-Related", "myofibrillar myopathy (disease) caused by mutation in DES", "autosomal recessive limb-girdle muscular dystrophy type 2R", "ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 7, FORMERLY", "arrhythmogenic right ventricular cardiomyopathy 7, formerly", "ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 7, FORMERLY", "arrhythmogenic right ventricular dysplasia, familial, 7, formerly", "CARDIOMYOPATHY, DILATED, WITH CONDUCTION DEFECT AND MUSCULAR DYSTROPHY", "cardiomyopathy, dilated, with conduction defect and muscular dystrophy", "cardiomyopathy, dilated, 1F and limb-girdle muscular dystrophy type 1D", "MYOFIBRILLAR MYOPATHY WITH ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY", "myofibrillar myopathy with arrhythmogenic right ventricular cardiomyopathy", "autosomal recessive limb-girdle muscular dystrophy caused by mutation in DES", "desmin-related myopathy with arrhythmogenic right ventricular cardiomyopathy", "DESMIN-RELATED MYOPATHY WITH ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY", "cardiomyopathy, dilated, 1F and limb-girdle muscular dystrophy type 1D, formerly", "CARDIOMYOPATHY, DILATED, 1F AND LIMB-GIRDLE MUSCULAR DYSTROPHY TYPE 1D, FORMERLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myofibrillar myopathy 1", "shortest_name_length": 3}
{"curie": "MONDO:0003762", "names": ["leptomeninx cancer", "cancer of leptomeninx", "leptomeningeal cancer", "malignant leptomeningeal tumor", "Malignant Leptomeningeal Tumor", "malignant leptomeninx neoplasm", "malignant leptomeningeal tumour", "malignant tumor of Leptomeninges", "malignant tumor of leptomeninges", "Malignant Tumor of Leptomeninges", "malignant tumour of Leptomeninges", "Malignant Leptomeningeal Neoplasm", "malignant neoplasm of leptomeninx", "malignant leptomeningeal neoplasm", "Malignant Neoplasm of Leptomeninges", "malignant neoplasm of leptomeninges", "Malignant Tumor of the Leptomeninges", "malignant tumor of the leptomeninges", "malignant neoplasm of the leptomeninges", "Malignant Neoplasm of the Leptomeninges"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant leptomeningeal tumor", "shortest_name_length": 18}
{"curie": "MONDO:0013424", "names": ["del(3p25)", "Monosomy 3p", "3p deletion", "monosomy 3p", "3p syndrome", "3p monosomy", "Deletion 3p", "deletion 3p", "3p- syndrome", "3p- SYNDROME", "deletion 3p25", "Monosomy 3pter", "monosomy 3pter", "del(3p) syndrome", "Del(3p) syndrome", "distal monosomy 3p", "Distal 3p deletion", "distal 3p deletion", "Distal monosomy 3p", "partial monosomy 3p", "3p deletion syndrome", "deletion 3p syndrome", "telomeric monosomy 3p", "Telomeric monosomy 3p", "chromosome 3p monosomy", "chromosome 3p deletion", "chromosome 3p- syndrome", "distal monosomy type 3p", "Chromosome 3, deletion 3p", "Chromosome 3, monosomy 3p", "chromosome 3, monosomy 3p25", "Distal monosomy 3p syndrome", "3p partial monosomy syndrome", "Chromosome 3p deletion syndrome", "chromosome 3p deletion syndrome", "Distal monosomy 3p syndrome (disorder)", "chromosome 3pter-p25 deletion syndrome", "chromosome 3pter-P25 deletion syndrome", "CHROMOSOME 3pter-p25 DELETION SYNDROME", "Distal monosomy 3p syndrome (diagnosis)", "3p partial monosomy syndrome (disorder)", "3p partial monosomy syndrome (diagnosis)", "deletion of part of chromosome distal monosomy 3p"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "3p- syndrome", "shortest_name_length": 9}
{"curie": "MONDO:0014026", "names": ["CSNB1F", "congenital stationary night blindness 1F", "LRIT3 congenital stationary night blindness", "congenital stationary night blindness type 1F", "night blindness, congenital stationary, type 1F", "NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1F", "congenital stationary night blindness - type 1f", "congenital stationary night blindness - type 1f (diagnosis)", "congenital stationary night blindness 1F autosomal recessive", "congenital stationary night blindness caused by mutation in LRIT3", "night blindness, congenital stationary (complete), 1F, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital stationary night blindness 1F", "shortest_name_length": 6}
{"curie": "UMLS:C4524741", "names": ["Pathologic Stage IVA Gastroesophageal Junction Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IVA Gastroesophageal Junction Adenocarcinoma AJCC v8", "shortest_name_length": 69}
{"curie": "MONDO:0003632", "names": ["Endocervicitis", "endocervicitis", "ENDOCERVICITIS", "endotrachelitis", "Endocervicitis, NOS", "endocervix inflammation", "Endocervicitis (disorder)", "inflammation of endocervix", "endocervicitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endocervicitis", "shortest_name_length": 14}
{"curie": "MONDO:0017168", "names": ["benign epithelial tumor of salivary glands"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign epithelial tumor of salivary glands", "shortest_name_length": 42}
{"curie": "UMLS:C4086163", "names": ["Childhood Mature Teratoma", "Childhood Mature Cystic Teratoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Mature Teratoma", "shortest_name_length": 25}
{"curie": "UMLS:C1334589", "names": ["Malignant Hemangiopericytoma NCI Grade 3", "Malignant Hemangiopericytoma NCI Grade III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Hemangiopericytoma NCI Grade 3", "shortest_name_length": 40}
{"curie": "MONDO:0015842", "names": ["bicornis uterus", "uterus bicornis", "Uterus bicornis", "uterus bicornate", "Bicornate uterus", "bicornate uterus", "uterus; bicornis", "bicornuate uterus", "UTERUS BICORNUATE", "bircornate uterus", "uterus bicornuate", "Bicornuate uterus", "Bicornuate Uterus", "heart shape uterus", "heart shaped uterus", "Heart shaped uterus", "uterus heart-shaped", "Heart-shaped uterus", "heart-shaped uterus", "Uterus heart-shaped", "Uterus heart shaped", "bicornis; bicornate uterus", "Bicornuate uterus (disorder)", "Uterus, bicornuate vetularum", "Uterus heart-shaped (finding)", "bicornuate uterus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bicornuate uterus", "shortest_name_length": 15}
{"curie": "MONDO:0100258", "names": ["PHYH deficiency", "phytanoyl-CoA hydroxylase deficiency", "PHYH related disorder of peroxisomal alpha oxidation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phytanoyl-CoA hydroxylase deficiency", "shortest_name_length": 15}
{"curie": "UMLS:C2987174", "names": ["VHL-Associated Pancreatic Serous Adenoma", "Von Hippel-Lindau Syndrome-Associated Pancreatic Serous Adenoma", "Von Hippel Lindau Syndrome-Associated Pancreatic Serous Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Von Hippel Lindau Syndrome-Associated Pancreatic Serous Adenoma", "shortest_name_length": 40}
{"curie": "MONDO:0003800", "names": ["Conventional Malignant Hemangiopericytoma", "conventional malignant hemangiopericytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "conventional malignant hemangiopericytoma", "shortest_name_length": 41}
{"curie": "MONDO:0014389", "names": ["PBMEI", "PGBM1", "polyglucosan body myopathy type 1", "Polyglucosan body myopathy type 1", "PGBM1 - polyglucosan body myopathy type 1", "Polyglucosan body myopathy type 1 (disorder)", "POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY", "polyglucosan body myopathy 1 with or without immunodeficiency", "polyglucosan body myopathy, early-onset, with or without immunodeficiency", "POLYGLUCOSAN BODY MYOPATHY, EARLY-ONSET, WITH OR WITHOUT IMMUNODEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyglucosan body myopathy 1 with or without immunodeficiency", "shortest_name_length": 5}
{"curie": "UMLS:C1370963", "names": ["Prostate cancer stage B", "Stage B Prostate Cancer", "stage B prostate cancer", "Stage B Prostatic Cancer", "prostate cancer, stage B", "Stage B Prostate Carcinoma", "Stage B Prostatic Carcinoma", "stage B cancer of the prostate", "cancer of the prostate, stage B", "stage B carcinoma of the prostate", "carcinoma of the prostate, stage B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate cancer stage B", "shortest_name_length": 23}
{"curie": "UMLS:C0155919", "names": ["lung; edema, acute", "edema; lung, acute", "Acute edema of lung", "Acute oedema of lung", "pulmonary acute edema", "PULMONARY EDEMA ACUTE", "Acute pulmonary edema", "acute edema pulmonary", "Acute Pulmonary Edema", "acute pulmonary edema", "acute pulmonary oedema", "Acute pulmonary oedema", "Oedema;pulmonary;acute", "Pulmonary edema - acute", "Pulmonary oedema - acute", "Acute edema of lung, NOS", "Acute oedema of lung, NOS", "Acute pulmonary edema NOS", "Acute pulmonary edema, NOS", "Acute pulmonary oedema, NOS", "Acute pulmonary edema syndrome", "Acute pulmonary edema (disorder)", "Acute edema of lung, unspecified", "acute pulmonary edema (diagnosis)", "Acute oedema of lung, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute pulmonary edema", "shortest_name_length": 18}
{"curie": "MONDO:0044793", "names": ["spitz nevi", "Spitz nevus", "Spitz Nevus", "spitz nevus", "spitz naevus", "juvenile nevus", "Juvenile nevus", "Juvenile Nevus", "Spindle cell nevus, NOS", "benign juvenile melanoma", "Benign Juvenile Melanoma", "Epithelioid and spindle cell nevus", "spindle and/ or epithelioid cell Nevus", "Spindle and/ or Epithelioid Cell Nevus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spitz nevus", "shortest_name_length": 10}
{"curie": "UMLS:C0342102", "names": ["Nipple deformity", "nipple deformity", "Nipple Deformity", "nipple; deformity", "deformity; nipple", "deformities nipple", "Nipple deformity (disorder)", "nipple deformity (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nipple Deformity", "shortest_name_length": 16}
{"curie": "UMLS:C3273133", "names": ["Bile Duct BilIN", "Intraductal BilIN", "Bile Duct Biliary Intraepithelial Neoplasia", "Intraductal Biliary Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bile Duct Biliary Intraepithelial Neoplasia", "shortest_name_length": 15}
{"curie": "MONDO:0004726", "names": ["liver inflammatory pseudotumor", "Liver Inflammatory Pseudotumor", "Inflammatory Pseudotumor of Liver", "inflammatory pseudotumor of liver", "Inflammatory pseudotumor of liver", "Inflammatory pseudotumour of liver", "Inflammatory Pseudotumor of the Liver", "Inflammatory pseudotumor of the liver", "inflammatory pseudotumor of the liver", "liver inflammatory myofibroblastic tumor", "Liver Inflammatory Myofibroblastic Tumor", "hepatic inflammatory myofibroblastic tumor", "Hepatic Inflammatory Myofibroblastic Tumor", "Inflammatory pseudotumor of liver (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "liver inflammatory myofibroblastic tumor", "shortest_name_length": 30}
{"curie": "MONDO:0030801", "names": ["M7MLS2", "monosomy 7 myelodysplasia and leukemia syndrome 2", "MONOSOMY 7 MYELODYSPLASIA AND LEUKEMIA SYNDROME 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "monosomy 7 myelodysplasia and leukemia syndrome 2", "shortest_name_length": 6}
{"curie": "UMLS:C0877046", "names": ["infection tooth", "Tooth Infection", "tooth infection", "Infection;tooth", "Tooth infection", "dental infection", "infection; tooth", "tooth; infection", "DENTAL INFECTION", "Dental Infection", "infections tooth", "infection dental", "Dental infection", "dental infections", "infection of tooth", "Infection of tooth", "Odontogenic infection", "Infection of tooth (disorder)", "infection of tooth (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tooth Infection", "shortest_name_length": 15}
{"curie": "MONDO:0007072", "names": ["ADULT syndrome", "ADULT SYNDROME", "Propping Zerres syndrome", "Pigment anomaly ectrodactyly hypodontia", "acrodermatounguallacrimaltooth syndrome", "Acro-dermato-ungual-lacrimal-tooth syndrome", "acro-dermato-ungual-lacrimal-Tooth syndrome", "acro-dermato-ungual-lacrimal-tooth syndrome", "ACRO-DERMATO-UNGUAL-LACRIMAL-TOOTH SYNDROME", "acro dermato ungual lacrimal tooth syndrome", "Pigment anomaly-ectrodactyly-hypodontia syndrome", "pigment anomaly-ectrodactyly-hypodontia syndrome", "ADULT (acro-dermato-ungual-lacrimal-tooth) syndrome", "Acro-dermato-ungual-lacrimal-tooth syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ADULT syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0007194", "names": ["AOVD1", "familial BAV", "aortic valve disease 1", "aortic valve disease type 1", "bicuspid aortic valve disease", "Familial bicuspid aortic valve", "familial bicuspid aortic valve"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial bicuspid aortic valve", "shortest_name_length": 5}
{"curie": "MONDO:0007000", "names": ["bejel", "Bejels", "Treponema pallidum", "treponemal disease", "Treponemal disease", "Treponema infection", "Treponema infections", "Treponemal infection", "Treponemal Infection", "treponemal infection", "Infection, Treponemal", "treponemal infections", "Treponemal Infections", "infection, Treponemal", "Infections, Treponemal", "infections, Treponemal", "Treponema infectious disease", "Treponema disease or disorder", "Treponema caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Treponema infectious disease", "shortest_name_length": 5}
{"curie": "MONDO:0014446", "names": ["BBS18", "BARDET-BIEDL SYNDROME 18", "Bardet-Biedl syndrome 18", "BBIP1 Bardet-Biedl syndrome", "Bardet-Biedl syndrome type 18", "Bardet-Biedl syndrome caused by mutation in BBIP1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bardet-Biedl syndrome 18", "shortest_name_length": 5}
{"curie": "MONDO:0007395", "names": ["CDHS", "Sommer-Young-Wee-Frye syndrome", "Sommer Young Wee Frye syndrome", "Craniofacial-Deafness-Hand Syndrome", "Craniofacial-deafness-hand syndrome", "craniofacial-deafness-hand syndrome", "CRANIOFACIAL-DEAFNESS-HAND SYNDROME", "craniofacial deafness hand syndrome", "Craniofacial deafness hand syndrome", "Craniofacial-hearing loss-hand syndrome", "Craniofacial deafness hand syndrome (disorder)", "features of flat facial profile, hypertelorism, hypoplastic nose with slitlike nares, and a sensorineural hearing loss"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniofacial-deafness-hand syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0015254", "names": ["Bilharzia", "bilharzia", "bilharzias", "Snail Fever", "snail fever", "Bilharziases", "bilharziasis", "blood flukes", "Bilharziasis", "BILHARZIASIS", "Katayama Fever", "Schistosomosis", "Fever, Katayama", "schistosomiasis", "Schistosomiases", "Schistosomiasis", "Blood flukes NOS", "Blood flukes, NOS", "Hemic distomiasis", "Haemic distomiasis", "Schistoma Infection", "fluke disease; blood", "Schistoma Infections", "blood; fluke disease", "Infection, Schistoma", "Blood fluke infection", "Infections, Schistoma", "Liver Fluke Infestation", "Infection by Schistosoma", "Unspecified schistosomiasis", "schistosomiasis (diagnosis)", "Schistosomiasis, unspecified", "Infection by Schistosoma, NOS", "Schistosomiasis [bilharziasis]", "Schistosomiasis (bilharziasis)", "Schistosomiasis - bilharziasis", "Disease due to Schistosomatidae", "Infection caused by Schistosoma", "Other specified schistosomiasis", "DISEASES DUE TO SCHISTOSOMATIDAE", "Disease caused by Schistosomatidae", "Infection caused by Schistosoma (disorder)", "Disease caused by Schistosomatidae (disorder)", "liver; disease, in schistosomiasis (bilharziasis) (etiology)", "liver; disease, in schistosomiasis (bilharziasis) (manifestation)", "disease (or disorder); liver, in schistosomiasis (bilharziasis) (etiology)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schistosomiasis", "shortest_name_length": 9}
{"curie": "UMLS:C4525614", "names": ["Duodenal Neuroendocrine Tumor by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Duodenal Neuroendocrine Tumor by AJCC v8 Stage", "shortest_name_length": 46}
{"curie": "UMLS:C4764084", "names": ["Recurrent Richter Syndrome", "Recurrent Transformed Chronic Lymphocytic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Transformed Chronic Lymphocytic Leukemia", "shortest_name_length": 26}
{"curie": "MONDO:0016897", "names": ["partial deletion of chromosome 19p", "partial monosomy of chromosome 19p", "partial deletion of the short arm of chromosome 19", "partial monosomy of the short arm of chromosome 19", "partial deletion of the short arm of chromosome type 19"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of the short arm of chromosome 19", "shortest_name_length": 34}
{"curie": "MONDO:0023662", "names": ["LMPHM10", "lymphatic malformation 10", "LYMPHATIC MALFORMATION 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphatic malformation 10", "shortest_name_length": 7}
{"curie": "MONDO:0033203", "names": ["SPLIS", "NPHS14", "nephrotic syndrome 14", "nephrotic syndrome type 14", "nephrotic syndrome, type 14", "NEPHROTIC SYNDROME, TYPE 14", "SPHINGOSINE PHOSPHATE LYASE INSUFFICIENCY SYNDROME", "familial steroid-resistant nephrotic syndrome with adrenal insufficiency", "primary adrenal insufficiency-steroid-resistant nephrotic syndrome due to SGPL1 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrotic syndrome 14", "shortest_name_length": 5}
{"curie": "MONDO:0012645", "names": ["GLC1N", "JOAG1N", "glaucoma 1, open angle, N", "Glaucoma 1, Open Angle, N", "GLAUCOMA 1, OPEN ANGLE, N", "GLAUCOMA 1, OPEN ANGLE, N (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glaucoma 1, open angle, N", "shortest_name_length": 5}
{"curie": "UMLS:C0854812", "names": ["Stage IV Lymphocyte Depleted Hodgkin Lymphoma", "Stage IV Hodgkin's Disease Lymphocyte Depleted", "Stage IV Lymphocyte Depleted Hodgkin's Lymphoma", "Hodgkin's disease lymphocyte depletion type stage IV", "Stage IV Hodgkin's Disease Lymphocyte Depletion Type", "Stage IV Hodgkin's Lymphoma Lymphocyte Depletion Type", "Stage IV Lymphocyte-Depleted Classical Hodgkin Lymphoma", "Stage IV Lymphocyte Depleted Classical Hodgkin Lymphoma", "Ann Arbor Stage IV Lymphocyte-Depleted Classic Hodgkin Lymphoma", "Ann Arbor Stage IV Lymphocyte-Depleted Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's disease lymphocyte depletion type stage IV", "shortest_name_length": 45}
{"curie": "UMLS:C1332595", "names": ["Borderline Ovarian Endometrioid Cystadenofibroma", "Borderline Malignancy Ovarian Endometrioid Cystadenofibroma", "Low Malignant Potential Ovarian Endometrioid Cystadenofibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Ovarian Endometrioid Cystadenofibroma", "shortest_name_length": 48}
{"curie": "MONDO:0008553", "names": ["BDPLT17", "platelet-type bleeding disorder 17", "Bleeding Disorder, Platelet-Type 17", "bleeding disorder, platelet-type 17", "bleeding disorder, platelet-type, 17", "BLEEDING DISORDER, PLATELET-TYPE, 17", "hereditary thrombasthenia-thrombocytopenia", "THROMBASTHENIA-THROMBOCYTOPENIA, HEREDITARY", "thrombasthenia-thrombocytopenia, hereditary", "Thrombasthenia-Thrombocytopenia, Hereditary", "GFI1B inherited bleeding disorder, platelet-type", "inherited bleeding disorder, platelet-type caused by mutation in GFI1B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "platelet-type bleeding disorder 17", "shortest_name_length": 7}
{"curie": "UMLS:C4727458", "names": ["Metastatic FLC", "Metastatic Fibrolamellar Carcinoma", "Metastatic Fibrolamellar Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Fibrolamellar Carcinoma", "shortest_name_length": 14}
{"curie": "MONDO:0008844", "names": ["Athrombia, essential", "Athrombia, Essential", "ATHROMBIA, ESSENTIAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Athrombia, essential", "shortest_name_length": 20}
{"curie": "UMLS:C5206835", "names": ["Malignant Parapharyngeal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Parapharyngeal Neoplasm", "shortest_name_length": 33}
{"curie": "UMLS:C0856023", "names": ["Splenic marginal zone lymphoma refractory", "Refractory Splenic Marginal Zone Lymphoma", "Refractory Splenic Marginal Zone B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Splenic marginal zone lymphoma refractory", "shortest_name_length": 41}
{"curie": "UMLS:C1332484", "names": ["Benign Pediatric Cerebral Tumor", "Benign Childhood Cerebral Tumor", "Benign Pediatric Cerebral Neoplasm", "Benign Childhood Tumor of Cerebrum", "Benign Pediatric Tumor of Cerebrum", "Benign Childhood Cerebral Neoplasm", "Childhood Benign Cerebral Neoplasms", "Benign Childhood Neoplasm of Cerebrum", "Benign Pediatric Neoplasm of Cerebrum", "Benign Childhood Tumor of the Cerebrum", "Benign Pediatric Tumor of the Cerebrum", "Benign Childhood Neoplasm of the Cerebrum", "Benign Pediatric Neoplasm of the Cerebrum", "Benign Pediatric Cerebral Hemispheric Tumor", "Benign Childhood Cerebral Hemispheric Tumor", "Benign Childhood Cerebral Hemispheric Neoplasm", "Benign Childhood Tumor of Cerebral Hemispheres", "Benign Pediatric Tumor of Cerebral Hemispheres", "Benign Pediatric Cerebral Hemispheric Neoplasm", "Benign Pediatric Neoplasm of Cerebral Hemispheres", "Benign Childhood Neoplasm of Cerebral Hemispheres", "Benign Pediatric Tumor of the Cerebral Hemispheres", "Benign Childhood Tumor of the Cerebral Hemispheres", "Benign Pediatric Neoplasm of the Cerebral Hemispheres", "Benign Childhood Neoplasm of the Cerebral Hemispheres"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Childhood Cerebral Neoplasm", "shortest_name_length": 31}
{"curie": "MONDO:0054852", "names": ["PSS6", "PEELING SKIN SYNDROME 6", "peeling skin syndrome 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peeling skin syndrome 6", "shortest_name_length": 4}
{"curie": "MONDO:0011880", "names": ["Fcnc", "FCNC", "CANDF3", "CANDN1", "Candidiasis, Familial, 3", "CANDIDIASIS, FAMILIAL, 3", "candidiasis, familial, 3", "CANDIDIASIS, FAMILIAL CHRONIC NAIL, WITH ICAM1 DEFICIENCY", "candidiasis, familial chronic nail, with Icam1 deficiency", "Candidiasis, Familial Chronic Nail, With ICAM1 Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "candidiasis, familial, 3", "shortest_name_length": 4}
{"curie": "UMLS:C0175166", "names": ["Skin and Connective Tissue Diseases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin and Connective Tissue Diseases", "shortest_name_length": 35}
{"curie": "MONDO:0100253", "names": ["RBS", "SC Phocomelia Syndrome", "pseudothalidomide syndrome", "Pseudothalidomide Syndrome", "Roberts-SC Phocomelia Syndrome", "Roberts-SC phocomelia syndrome", "Phocomelia-Pseudothalidomide Syndrome", "phocomelia-pseudothalidomide syndrome", "Hypomelia Hypotrichosis Facial Hemangioma Syndrome", "long bone deficiencies associated with cleft lip-palate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Roberts-SC phocomelia syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0015998", "names": ["IEL", "lens; ectopia", "ectopia; lens", "Lens luxation", "lens luxation", "lens luxations", "Ectopia Lentis", "Ectopia lentis", "dislocated lens", "Lentis, Ectopia", "Dislocated lens", "Lens Dislocation", "lens dislocation", "dislocation lens", "LENS DISLOCATION", "luxation of lens", "Lens dislocation", "DISLOCATION, LENS", "dislocation; lens", "lens dislocations", "Lens Dislocations", "Dislocated lenses", "lens; dislocation", "Dislocation, Lens", "Dislocations, Lens", "dislocation of lens", "Dislocation of lens", "Luxation of lens, NOS", "Congenital ectopic lens", "isolated ectopia lentis", "congenital ectopic lens", "ectopia lentis syndrome", "Congenital Ectopic Lens", "familial ectopia lentis", "Familial ectopia lentis", "Ectopia Lentis, Familial", "Dislocation of lens, NOS", "congenital displaced lens", "Congenital displaced lens", "Congenitally displaced lens", "Abnormality of lens position", "Crystalline Lens Dislocation", "dislocation; lens, congenital", "lens; dislocation, congenital", "Congenital dislocation of lens", "isolated lens position anomaly", "Congenital subluxation of lens", "Unspecified dislocation of lens", "dislocation of lens (diagnosis)", "nonsyndromic lens position anomaly", "Congenital ectopic lens (disorder)", "congenital ectopic lens (diagnosis)", "congenital displaced lens (diagnosis)", "dislocation of lens (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated ectopia lentis", "shortest_name_length": 3}
{"curie": "MONDO:0010087", "names": ["SUGARMAN BRACHYDACTYLY", "Sugarman brachydactyly", "Sugarman Hager Kulik syndrome", "Sugarman-Hager-Kulik syndrome", "Sugarman brachydactyly (disorder)", "BRACHYDACTYLY WITH MAJOR PROXIMAL PHALANGEAL SHORTENING", "Brachydactyly with major proximal phalangeal shortening", "brachydactyly with Major proximal phalangeal shortening", "brachydactyly with major proximal phalangeal shortening", "brachydactyly of the hands and feet with duplication of the first toes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sugarman brachydactyly", "shortest_name_length": 22}
{"curie": "MONDO:0007528", "names": ["EDS, unspecified type", "EDS, UNSPECIFIED TYPE", "Ehlers-Danlos Syndrome, Friedman-Harrod Type", "EHLERS-DANLOS SYNDROME, FRIEDMAN-HARROD TYPE", "Ehlers-Danlos syndrome, Friedman-Harrod type", "Ehlers-Danlos Syndrome, Autosomal Dominant, Type Unspecified", "Ehlers-Danlos syndrome, autosomal dominant, type unspecified", "EHLERS-DANLOS SYNDROME, AUTOSOMAL DOMINANT, TYPE UNSPECIFIED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ehlers-Danlos syndrome, autosomal dominant, type unspecified", "shortest_name_length": 21}
{"curie": "MONDO:0017181", "names": ["hypnic headache", "Hypnic headache", "Hypnic Headache", "Headache, Hypnic", "Alarm Clock Headache", "Alarm clock headache", "Alarm Clock Headaches", "Clock Headache, Alarm", "Headache, Alarm Clock", "Clock Headaches, Alarm", "Headaches, Alarm Clock", "Hypnic Headache Syndrome", "Hypnic Headache Syndromes", "Headache Syndrome, Hypnic", "Primary Headache Disorder", "hypnic headache (disease)", "Disorder, Primary Headache", "Headache Syndromes, Hypnic", "Headache Disorder, Primary", "Primary Headache Disorders", "Hypnic headache (disorder)", "Disorders, Primary Headache", "Headache Disorders, Primary", "hypnic headache (diagnosis)", "Hypnic headache (associated with sleep)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypnic headache", "shortest_name_length": 15}
{"curie": "MONDO:0044079", "names": ["Renocardiac Syndrome", "Cardiorenal Syndrome", "cardiorenal syndrome", "Cardiorenal syndrome", "Renocardiac syndrome", "Renocardiac syndromes", "Reno-Cardiac Syndrome", "cardio-renal syndrome", "syndrome, cardiorenal", "Cardio-Renal Syndrome", "Cardiorenal Syndromes", "Reno-Cardiac syndrome", "Reno Cardiac Syndrome", "Syndrome, Cardiorenal", "Renocardiac Syndromes", "cardio renal syndrome", "Syndrome, Renocardiac", "cardiorenal syndromes", "syndrome, Renocardiac", "Cardio Renal Syndrome", "Reno Cardiac syndrome", "syndromes, Renocardiac", "Cardio-Renal Syndromes", "Reno-Cardiac Syndromes", "syndromes, cardiorenal", "Syndrome, Reno-Cardiac", "Syndromes, Cardiorenal", "cardio-renal syndromes", "syndrome, cardio-renal", "syndrome, Reno-Cardiac", "Syndrome, Cardio-Renal", "Reno-Cardiac syndromes", "Syndromes, Renocardiac", "syndromes, cardio-renal", "Syndromes, Cardio-Renal", "Syndromes, Reno-Cardiac", "syndromes, Reno-Cardiac", "Cardiorenal syndrome (disorder)", "cardiorenal syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardio-renal syndrome", "shortest_name_length": 20}
{"curie": "UMLS:C3899346", "names": ["Disseminated Listeriosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disseminated Listeriosis", "shortest_name_length": 24}
{"curie": "MONDO:0014618", "names": ["RP71", "RETINITIS PIGMENTOSA 71", "retinitis pigmentosa 71", "IFT172 retinitis pigmentosa", "retinitis pigmentosa type 71", "retinitis pigmentosa caused by mutation in IFT172"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 71", "shortest_name_length": 4}
{"curie": "MONDO:0013776", "names": ["SPAX5", "spastic ataxia 5", "spastic ataxia type 5", "spastic ataxia 5, autosomal recessive", "SPASTIC ATAXIA 5, AUTOSOMAL RECESSIVE", "AFG3L2 autosomal recessive spastic ataxia", "autosomal recessive spastic ataxia type 5", "Autosomal recessive spastic ataxia type 5", "AFG3L2-related spastic ataxia-neuropathy syndrome", "autosomal recessive spastic ataxia caused by mutation in AFG3L2", "early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome", "Early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome", "early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome", "Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome", "AFG3L2-related spastic ataxia-myoclonic epilepsy-neuropathy syndrome", "AFG3L2-related spastic ataxia, myoclonic epilepsy, neuropathy syndrome", "Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder)", "early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (diagnosis)", "AFG3L2 (AFG3 like matrix AAA peptidase subunit 2) related spastic ataxia, myoclonic epilepsy, neuropathy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic ataxia 5", "shortest_name_length": 5}
{"curie": "MONDO:0023868", "names": ["melanoma associated retinopathy", "Melanoma-Associated Retinopathy", "Melanoma-associated retinopathy", "Melanoma Associated Retinopathy", "Melanoma associated retinopathy", "Retinopathy, Melanoma-Associated", "Melanoma-Associated Retinopathies", "Retinopathies, Melanoma-Associated", "Melanoma-associated retinopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melanoma associated retinopathy", "shortest_name_length": 31}
{"curie": "MONDO:0000389", "names": ["atelosteogenesis", "Atelosteogenesis", "Giant cell chondrodysplasia", "Atelosteogenesis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atelosteogenesis", "shortest_name_length": 16}
{"curie": "MONDO:0003906", "names": ["hepatoid pattern ovarian yolk sac tumor", "ovarian yolk Sac tumor, hepatoid pattern", "ovarian yolk sac tumor, hepatoid pattern", "Ovarian Yolk Sac Tumor, Hepatoid Pattern"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian yolk sac tumor, hepatoid pattern", "shortest_name_length": 39}
{"curie": "MONDO:0004452", "names": ["childhood CNS germinoma", "childhood intracranial germinoma", "Central nervous system germinoma", "Central Nervous System Germinoma", "Childhood Central Nervous System Germinoma", "childhood central nervous system germinoma", "pediatric central nervous system germinoma", "central nervous system germinoma of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood central nervous system germinoma", "shortest_name_length": 23}
{"curie": "MONDO:0020285", "names": ["transposition of the great arteries and conotruncal cardiac anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transposition of the great arteries and conotruncal cardiac anomaly", "shortest_name_length": 67}
{"curie": "MONDO:0021081", "names": ["NMDARE", "Anti-NMDAR Encephalitis", "Anti NMDAR Encephalitis", "Encephalitis, Anti-NMDAR", "Anti-NMDAR Encephalitides", "Encephalitides, Anti-NMDAR", "NMDA receptor encephalitis", "Anti NMDA Receptor Encephalitis", "Anti-NMDA receptor encephalitis", "anti-NMDA receptor encephalitis", "Anti-NMDA Receptor Encephalitis", "Encephalitis, Anti-NMDA Receptor", "Receptor Encephalitis, Anti-NMDA", "Anti-NMDA Receptor Encephalitides", "Receptor Encephalitides, Anti-NMDA", "Encephalitides, Anti-NMDA Receptor", "N-methyl-D-aspartate receptor encephalitis", "Anti N Methyl D Aspartate Receptor Encephalitis", "Anti-N-Methyl-D-Aspartate Receptor Encephalitis", "Encephalitis, Anti-N-Methyl-D-Aspartate Receptor", "Anti-N-Methyl-D-Aspartate Receptor Encephalitides", "limbic encephalitis with NMDA receptor antibodies", "Limbic encephalitis with NMDA receptor antibodies", "Encephalitides, Anti-N-Methyl-D-Aspartate Receptor", "Anti-NMDA (N-methyl D-Aspartate) receptor encephalitis", "Limbic encephalitis with N-methyl-D-aspartate receptor antibodies", "limbic encephalitis with N-methyl-D-aspartate receptor antibodies", "Autoimmune encephalitis caused by N-methyl-D-aspartate receptor antibody", "Autoimmune encephalitis caused by N-methyl D-aspartate receptor antibody", "Limbic encephalitis with N-methyl-D-aspartate receptor antibodies (disorder)", "Autoimmune encephalitis caused by N-methyl-D-aspartate receptor antibody (disorder)", "Autoimmune encephalitis caused by N-methyl D-aspartate receptor antibody (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anti-NMDA receptor encephalitis", "shortest_name_length": 6}
{"curie": "UMLS:C1298681", "names": ["Oxalosis", "oxalosis", "Oxalosis (disorder)", "oxalosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oxalosis", "shortest_name_length": 8}
{"curie": "MONDO:0003423", "names": ["middle ear adenoma", "Middle Ear Adenoma", "Adenoma of Middle Ear", "adenoma of middle ear", "Adenoma of middle ear", "adenoma of the middle ear", "Adenoma of the Middle Ear", "Adenoma of middle ear (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "middle ear adenoma", "shortest_name_length": 18}
{"curie": "MONDO:0001317", "names": ["Phlyctenulosis", "phlyctenulosis", "Strumous ophthalmia", "strumous ophthalmia", "phlyctenular keratitis", "Phlyctenular keratitis", "Phlyctenular ophthalmia", "phlyctenular keratoconjunctivitis", "Phlyctenular keratoconjunctivitis", "phlyctenular; keratoconjunctivitis", "keratoconjunctivitis; phlyctenular", "Phlyctenular keratoconjunctivitis (disorder)", "phlyctenular keratoconjunctivitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phlyctenulosis", "shortest_name_length": 14}
{"curie": "UMLS:C1536081", "names": ["Vascular stent thrombosis", "Vascular scaffold thrombosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vascular stent thrombosis", "shortest_name_length": 25}
{"curie": "UMLS:C4524897", "names": ["stage IIB anal cancer", "Stage IIB Anal Cancer", "stage IIB anal cancer AJCC v8", "Stage IIB Anal Cancer AJCC v8", "stage IIB anal carcinoma AJCC v8", "Stage IIB Anal Carcinoma AJCC v8", "Stage IIB Anal Canal and Perianal (Anal Margin) Carcinoma AJCC v8", "stage IIB anal canal and perianal (anal margin) carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Anal Cancer AJCC v8", "shortest_name_length": 21}
{"curie": "UMLS:C0423778", "names": ["scabs skin", "Skin Eschar", "Skin eschar", "skin eschar", "scabbed skin", "scabbing skin", "Skin eschar (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin eschar", "shortest_name_length": 10}
{"curie": "UMLS:C4744717", "names": ["Locally Advanced Unresectable Prostate Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Unresectable Prostate Adenocarcinoma", "shortest_name_length": 53}
{"curie": "UMLS:C0346993", "names": ["breast neoplasm malignant female secondary", "Secondary malignant neoplasm of female breast", "Metastatic malignant neoplasm of female breast", "Metastatic malignant neoplasm to female breast", "Secondary malignant neoplasm of female breast, NOS", "Metastatic malignant neoplasm to female breast, NOS", "Metastatic malignant neoplasm to female breast (disorder)", "Secondary malignant neoplasm of female breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary malignant neoplasm of female breast", "shortest_name_length": 42}
{"curie": "MONDO:0000942", "names": ["cornea", "cornea disease", "disease cornea", "cornea diseases", "cornea disorder", "Corneal Disease", "corneal disease", "cornea; disorder", "Disease, Corneal", "DISORDER CORNEAL", "Corneal disorder", "Corneal Disorder", "Disorder corneal", "cornea disorders", "diseases corneal", "corneal disorder", "Corneal Diseases", "Cornea--Diseases", "corneal diseases", "Corneal Disorders", "Diseases, Corneal", "disease of cornea", "corneal disorders", "DISEASE OF CORNEA", "CORNEAL DISORDERS", "disorder of cornea", "Disorder of cornea", "Corneal disorder NOS", "diseases of the cornea", "CORNEAL DISORDER (NOS)", "DISEASES OF THE CORNEA", "Disease of cornea, NOS", "Disorder of cornea, NOS", "cornea disease or disorder", "Unspecified corneal disorder", "corneal disorder (diagnosis)", "disease or disorder of cornea", "Disorder of cornea (disorder)", "disease (or disorder); cornea", "Unspecified disorder of cornea", "Disorder of cornea, unspecified", "DISEASES OF THE CORNEA AND CONJUNCTIVA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal disorder", "shortest_name_length": 6}
{"curie": "UMLS:C0086404", "names": ["Experimental Hepatoma", "Experimental Hepatomas", "Hepatoma, Experimental", "Hepatomas, Experimental"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Experimental Hepatoma", "shortest_name_length": 21}
{"curie": "UMLS:C3827194", "names": ["Glioblastoma by Gene Expression Profile"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Glioblastoma by Gene Expression Profile", "shortest_name_length": 39}
{"curie": "MONDO:0013226", "names": ["ROCHIS", "ROIFMAN-CHITAYAT SYNDROME", "Roifman-Chitayat Syndrome", "ROIFMAN-Chitayat syndrome", "Roifman-Chitayat syndrome", "Roifman Chitayat syndrome", "Roifman-Chitayat syndrome, digenic", "combined immunodeficiency with faciooculoskeletal anomalies", "Combined immunodeficiency with faciooculoskeletal anomalies", "Combined immunodeficiency with faciooculoskeletal anomalies syndrome", "Combined immunodeficiency with faciooculoskeletal anomalies syndrome (disorder)", "combined immunodeficiency, Facial Dysmorphism, optic nerve atrophy, skeletal anomalies, and developmental delay", "Combined Immunodeficiency, Facial Dysmorphism, Optic Nerve Atrophy, Skeletal Anomalies, And Developmental Delay", "COMBINED IMMUNODEFICIENCY, FACIAL DYSMORPHISM, OPTIC NERVE ATROPHY, SKELETAL ANOMALIES, AND DEVELOPMENTAL DELAY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined immunodeficiency with faciooculoskeletal anomalies", "shortest_name_length": 6}
{"curie": "UMLS:C1697538", "names": ["Infusion site hemorrhage", "Infusion site haemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infusion site hemorrhage", "shortest_name_length": 24}
{"curie": "MONDO:0007219", "names": ["BDA6", "Brachydactyly type A6", "brachydactyly type A6", "Brachydactyly, Type A6", "BRACHYDACTYLY, TYPE A6", "brachydactyly, type A6", "OSEBOLD-Remondini syndrome", "Osebold-Remondini syndrome", "OSEBOLD-REMONDINI SYNDROME", "Osebold Remondini syndrome", "Brachydactyly type A6 (disorder)", "BRACHYMESOPHALANGY WITH MESOMELIC SHORT LIMBS AND CARPAL AND TARSAL OSSEOUS ABNORMALITIES", "Brachymesophalangy with mesomelic short limbs and carpal and tarsal osseous abnormalities", "brachymesophalangy with mesomelic short limbs and carpal and tarsal osseous abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Osebold-Remondini syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0410256", "names": ["Muscle injury", "muscle injury", "muscle; injury", "injury; muscle", "muscle injuries", "Muscular injury", "muscular injury", "Muscle injuries", "injury of muscle", "Injury of muscle", "Muscle injury NOS", "Muscle injury, NOS", "Injury of muscle, NOS", "Injury of muscle (disorder)", "injury of muscle (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscle injury", "shortest_name_length": 13}
{"curie": "UMLS:C0235222", "names": ["dia htn", "diastolic htn", "dia hypertension", "Hypertension diastolic", "DIASTOLIC HYPERTENSION", "diastolic hypertension", "HYPERTENSION DIASTOLIC", "Diastolic Hypertension", "hypertension diastolic", "Diastolic hypertension", "Hypertension, diastolic", "Diastolic hypertension, NOS", "Diastolic hypertension (disorder)", "BLOOD PRESSURE INCREASE DIASTOLIC", "diastolic hypertension (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diastolic hypertension", "shortest_name_length": 7}
{"curie": "UMLS:C3266735", "names": ["Hemodialysis Catheter Infection", "Infection of hemodialysis catheter", "Infection of hemodialysis catheter (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infection of hemodialysis catheter", "shortest_name_length": 31}
{"curie": "MONDO:0010211", "names": ["XPC", "XP3", "XP-C", "XPCC", "XP group C", "XP, GROUP C", "XP, Group C", "xeroderma pigmentosum 3", "xeroderma pigmentosum III", "Xeroderma Pigmentosum III", "XERODERMA PIGMENTOSUM III", "Xeroderma Pigmentosum Group C", "Xeroderma pigmentosum group C", "xeroderma pigmentosum group C", "xeroderma pigmentosum, type 3", "xeroderma pigmentosum, group C", "Xeroderma pigmentosum, group C", "xeroderma pigmentosum group type C", "Xeroderma pigmentosum, group C (disorder)", "xeroderma pigmentosum, complementation group C", "XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C", "Xeroderma Pigmentosum, Complementation Group C", "xeroderma pigmentosum, complementation group type C"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "xeroderma pigmentosum group C", "shortest_name_length": 3}
{"curie": "MONDO:0008242", "names": ["Herrmann syndrome", "HERRMANN SYNDROME", "Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction", "photomyoclonus, diabetes mellitus, deafness, nephropathy, and cerebral dysfunction", "PHOTOMYOCLONUS, DIABETES MELLITUS, DEAFNESS, NEPHROPATHY, AND CEREBRAL DYSFUNCTION", "Photomyoclonus, Diabetes Mellitus, Deafness, Nephropathy, And Cerebral Dysfunction", "Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction (disorder)", "hereditary photomyoclonus associated with diabetes mellitus, deafness, nephropathy, and cerebral dysfunction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "photomyoclonus, diabetes mellitus, deafness, nephropathy, and cerebral dysfunction", "shortest_name_length": 17}
{"curie": "MONDO:0030720", "names": ["Trichomonal leukorrhea", "trichomonal leukorrhea", "Trichomonal leukorrhoea", "Vulvovaginitis trichomonal", "trichomonas vulvovaginitis", "trichomonal vulvovaginitis", "Trichomonal vulvovaginitis", "leukorrhea vaginalis - trichomonal", "Leukorrhea vaginalis - trichomonal", "Leukorrhoea vaginalis - trichomonal", "Trichomonas vaginalis vulvovaginitis", "Trichomonal vulvovaginitis (disorder)", "trichomonal vulvovaginitis (diagnosis)", "Trichomonas vaginalis caused vulvovaginitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichomonal vulvovaginitis", "shortest_name_length": 22}
{"curie": "UMLS:C0752180", "names": ["bacterial CNS infection", "Central Nervous System Bacterial Infections", "Bacterial Infections, Central Nervous System", "Bacterial infection of central nervous system", "Infections, Bacterial, Central Nervous System", "Bacterial infection of central nervous system (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Bacterial Infections", "shortest_name_length": 23}
{"curie": "UMLS:C0848648", "names": ["Fungal rash", "Rash;fungal", "fungal rash", "Fungal rash NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fungal rash", "shortest_name_length": 11}
{"curie": "UMLS:C0521158", "names": ["Recurrent", "recurrence", "Recurrence", "Recurrent Tumor", "recurrent tumor", "Recurrent tumor", "Recurrent tumour", "recurrence tumor", "tumor recurrence", "recurrences tumor", "Recurrent neoplasm", "Recurrent Neoplasm", "neoplasm recurrence", "Neoplasm Recurrence", "Recurrence of tumor", "Neoplasm recurrence", "Recurrence of tumour", "Neoplasm recurrence NOS", "NEOPLASM RECURRENCE NOS", "Recurrent neoplasm (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent tumor", "shortest_name_length": 9}
{"curie": "MONDO:0001472", "names": ["TLYM", "Lymphoma of Testis", "lymphoma of testis", "testicular lymphoma", "Testicular Lymphoma", "Lymphoma of the Testis", "lymphoma of the testis", "primary testicular lymphoma", "Primary Testicular Lymphoma", "malignant lymphoma of testis", "Malignant lymphoma of testis", "Malignant lymphoma of testis (disorder)", "malignant lymphoma of testis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular lymphoma", "shortest_name_length": 4}
{"curie": "MONDO:0002594", "names": ["Mpox", "mpox", "monkeypox", "Monkeypox", "monkey pox", "Monkey Pox", "Monkey pox", "Monkeypox disease", "Monkeypox (disorder)", "monkeypox (diagnosis)", "Monkeypox virus infection", "infections, Monkeypox virus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "monkeypox", "shortest_name_length": 4}
{"curie": "UMLS:C0542237", "names": ["Thrombophlebitis injection site", "Injection site thrombophlebitis", "THROMBOPHLEBITIS INJECTION SITE", "Injection Site Thrombophlebitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site thrombophlebitis", "shortest_name_length": 31}
{"curie": "UMLS:C0334418", "names": ["Malignant nonchromaffin paraganglioma", "Malignant extra-adrenal paraganglioma", "malignant extra-adrenal paraganglioma", "Malignant Extra-Adrenal Paraganglioma", "Metastatic Extra-Adrenal Paraganglioma", "Nonchromaffin paraganglioma, malignant", "Malignant non-chromaffin paraganglioma", "Extra-adrenal paraganglioma, malignant", "malignant extra-adrenal paraganglioma (diagnosis)", "Extra-adrenal paraganglioma, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extra-adrenal paraganglioma, malignant", "shortest_name_length": 37}
{"curie": "UMLS:C1710400", "names": ["Thymic Lipofibroadenoma", "Thymus Lipofibroadenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thymus Lipofibroadenoma", "shortest_name_length": 23}
{"curie": "MONDO:0000969", "names": ["pleura lipoma", "pleural lipoma", "Pleural lipoma", "Pleural Lipoma", "Lipoma of pleura", "lipoma of pleura", "Lipoma of Pleura", "Lipoma of the Pleura", "lipoma of the pleura", "Lipoma of pleura (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pleural lipoma", "shortest_name_length": 13}
{"curie": "MONDO:0004994", "names": ["CARDIOMYOPATHY", "Myocardiopathy", "cardiomyopathy", "myocardiopathy", "Cardiomyopathy", "Cardiomyopathy,", "CARDIOMYOPATHIES", "Cardiomyopathies", "cardiomyopathies", "Myocardiopathies", "Myocardiodystrophy", "Cardiomyopathy NOS", "myocardial disease", "Myocardial Disease", "Myocardial disease", "myocardial diseases", "Myocardiopathy, NOS", "Myocardial Diseases", "myocardium; disease", "myocardium disorder", "Cardiomyopathy, NOS", "Disease, Myocardial", "heart muscle disease", "Diseases, Myocardial", "Myocardium--Diseases", "heart muscle disorder", "disorder of myocardium", "Disorder of myocardium", "Myocardial disease, NOS", "Cardiomyopathy;secondary", "Disorder of heart muscle", "CARDIOMYOPATHY SECONDARY", "cardiomyopathy secondary", "secondary cardiomyopathy", "Secondary Cardiomyopathy", "Secondary cardiomyopathy", "Cardiomyopathy secondary", "Cardiomyopathy, Secondary", "cardiomyopathy; secondary", "Cardiomyopathy (disorder)", "secondary; cardiomyopathy", "Secondary Cardiomyopathies", "cardiomyopathy (diagnosis)", "cardiomyopathies secondary", "Cardiomyopathies, Secondary", "Disease of the heart muscle", "Cardiomyopathy, unspecified", "Secondary Myocardial Disease", "Cardiomyopathy secondary NOS", "Myocardial disease (disorder)", "Secondary cardiomyopathy, NOS", "Myocardial Disease, Secondary", "Disease, Secondary Myocardial", "Secondary Myocardial Diseases", "Myocardial Diseases, Secondary", "Diseases, Secondary Myocardial", "secondary cardiomyopathy (diagnosis)", "Secondary cardiomyopathy, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiomyopathy", "shortest_name_length": 14}
{"curie": "UMLS:C0919659", "names": ["oropharyngeal thrush", "candidiasis oropharyngeal", "Oropharyngeal Candidiasis", "Oropharyngeal candidiasis", "oropharyngeal candidiasis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oropharyngeal candidiasis", "shortest_name_length": 20}
{"curie": "UMLS:C0863183", "names": ["Recurrent Larynx Cancer", "larynx cancer, recurrent", "Relapsed Larynx Carcinoma", "recurrent laryngeal cancer", "Larynx carcinoma recurrent", "Recurrent Larynx Carcinoma", "Recurrent Laryngeal Cancer", "Carcinoma larynx recurrent", "laryngeal cancer, recurrent", "Relapsed Laryngeal Carcinoma", "Relapsed Carcinoma of Larynx", "Recurrent Carcinoma of Larynx", "Recurrent Laryngeal Carcinoma", "Carcinoma of larynx recurrent", "Relapsed Carcinoma of the Larynx", "Recurrent Carcinoma of the Larynx", "Recurrent Laryngeal Throat Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carcinoma larynx recurrent", "shortest_name_length": 23}
{"curie": "UMLS:C5237056", "names": ["Recurrent Moderate-Severe Chronic Graft Versus Host Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Moderate-Severe Chronic Graft Versus Host Disease", "shortest_name_length": 59}
{"curie": "MONDO:0009728", "names": ["Nph1", "NPH1", "NPHP1", "nephronophthisis 1", "NEPHRONOPHTHISIS 1", "Nephronophthisis 1", "Type 1 nephronophthisis", "nephronophthisis type 1", "Juvenile Nephronophthisis", "juvenile nephronophthisis", "Juvenile nephronophthisis", "juvenile nephronophthisis 1", "nephronophthisis 1, juvenile", "NPHP1 nephronophthisis (disease)", "familial juvenile nephronophthisis", "Familial juvenile nephronophthisis", "Familial Juvenile Nephronophthisis", "Nephronophthisis, familial juvenile", "nephronophthisis, familial juvenile", "NEPHRONOPHTHISIS, FAMILIAL JUVENILE", "Juvenile nephronophthisis (disorder)", "Familial juvenile medullary cystic kidney disease", "nephronophthisis (disease) caused by mutation in NPHP1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephronophthisis 1", "shortest_name_length": 4}
{"curie": "MONDO:0008342", "names": ["Pubic Bone Dysplasia", "PUBIC BONE DYSPLASIA", "pubic bone dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pubic bone dysplasia", "shortest_name_length": 20}
{"curie": "MONDO:0007135", "names": ["NDNC6", "anonychia, partial", "ANONYCHIA, PARTIAL", "onychodystrophy-anonychia", "absent nails and dystrophic nails", "nonsyndromic congenital nail disorder 6", "ANONYCHIA/HYPONYCHIA AND ONYCHODYSTROPHY", "anonychia/hyponychia and onychodystrophy", "nail disorder, nonsyndromic congenital, 6", "NAIL DISORDER, NONSYNDROMIC CONGENITAL, 6", "nonsyndromic congenital nail disorder type 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nonsyndromic congenital nail disorder 6", "shortest_name_length": 5}
{"curie": "UMLS:C5447837", "names": ["Bladder Flat Urothelial Carcinoma", "Bladder Sessile Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder Flat Urothelial Carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0003809", "names": ["mediastinum spindle cell tumor", "mediastinum hemangiopericytoma", "malignant mediastinum hemangiopericytoma", "Malignant Mediastinal Hemangiopericytoma", "malignant mediastinal hemangiopericytoma", "Malignant Hemangiopericytoma of Mediastinum", "malignant hemangiopericytoma of mediastinum", "malignant hemangiopericytoma of the mediastinum", "Malignant Hemangiopericytoma of the Mediastinum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant mediastinum hemangiopericytoma", "shortest_name_length": 30}
{"curie": "MONDO:0008119", "names": ["CPD1", "SCA1", "Sca1", "OPCA4", "OPCA1", "SCA1s", "OPCA I", "OPCA 1", "OPCA 4", "OPCA IV", "Menzel type OPCA", "MENZEL TYPE OPCA", "Menzel Type OPCA", "OPCA, Menzel Type", "SPINOCEREBELLAR ATAXIA 1", "Schut Haymaker Type OPCA", "Spinocerebellar Ataxia 1", "SCHUT-HAYMAKER TYPE OPCA", "Spinocerebellar Ataxia-1", "spinocerebellar ataxia 1", "Schut-Haymaker Type OPCA", "Schut-haymaker type OPCA", "SPINOCEREBELLAR ATROPHY I", "Ataxia 1, Spinocerebellar", "OPCA, Schut-Haymaker Type", "Spinocerebellar Ataxia 1s", "Spinocerebellar Atrophy I", "spinocerebellar atrophy 1", "Spinocerebellar Atrophy Is", "Atrophy I, Spinocerebellar", "Spinocerebellar Ataxia Type 1", "Spinocerebellar ataxia type 1", "Type 1 Spinocerebellar Ataxia", "spinocerebellar ataxia type 1", "OLIVOPONTOCEREBELLAR ATROPHY I", "olivopontocerebellar atrophy 1", "olivopontocerebellar atrophy 4", "Olivopontocerebellar Atrophy I", "Cerebelloparenchymal Disorder I", "OLIVOPONTOCEREBELLAR ATROPHY IV", "cerebelloparenchymal disorder 1", "CEREBELLOPARENCHYMAL DISORDER I", "Atrophy I, Olivopontocerebellar", "Olivopontocerebellar Atrophy Is", "Olivopontocerebellar Atrophy IV", "Olivopontocerebellar Atrophy IVs", "Atrophy IV, Olivopontocerebellar", "Cerebelloparenchymal Disorder Is", "Atrophy IVs, Olivopontocerebellar", "Spinocerebellar ataxia type 1 (disorder)", "ATXN1 autosomal dominant cerebellar ataxia type I", "autosomal dominant cerebellar ataxia type I caused by mutation in ATXN1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia type 1", "shortest_name_length": 4}
{"curie": "UMLS:C1512431", "names": ["High Grade B-Cell Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade B-Cell Non-Hodgkin's Lymphoma", "shortest_name_length": 40}
{"curie": "MONDO:0006214", "names": ["FVPTC", "Papillary carcinoma, follicular variant", "Papillary Thyroid Carcinoma, Follicular Variant", "Follicular Variant Thyroid Gland Papillary Carcinoma", "follicular variant thyroid gland papillary carcinoma", "follicular variant papillary carcinoma of thyroid gland", "follicular variant papillary carcinoma of the thyroid gland", "follicular variant papillary carcinoma of the thyroid gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "follicular variant thyroid gland papillary carcinoma", "shortest_name_length": 5}
{"curie": "MONDO:0026724", "names": ["MRXSPM", "Paganini-Miozzo syndrome", "PAGANINI-MIOZZO SYNDROME", "Paganini-Miozzo syndrome, X-linked recessive", "MENTAL RETARDATION, X-LINKED, SYNDROMIC, PAGANINI-MIOZZO TYPE", "mental retardation, X-Linked, syndromic, Paganini-Miozzo type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paganini-Miozzo syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C1395365", "names": ["Dialysis Catheter Embolism", "embolism; dialysis catheter", "dialysis catheter; embolism", "embolism; catheter, dialysis catheter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dialysis Catheter Embolism", "shortest_name_length": 26}
{"curie": "UMLS:C5556339", "names": ["Recurrent Multinodular and Vacuolated Neuronal Tumor", "Recurrent Multinodular and Vacuolating Neuronal Tumor", "Recurrent Multinodular and Vacuolated Tumor of the Cerebrum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Multinodular and Vacuolated Neuronal Tumor", "shortest_name_length": 52}
{"curie": "UMLS:C5418815", "names": ["Refractory Malignant Mastocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Malignant Mastocytosis", "shortest_name_length": 33}
{"curie": "MONDO:0012440", "names": ["Mgr10", "MGR10", "migraine with pulsation", "MIGRAINE WITH PULSATION", "migraine with or without aura, susceptibility to, 10", "MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 10", "migraine with or without aura, susceptibility to, type 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "migraine with or without aura, susceptibility to, 10", "shortest_name_length": 5}
{"curie": "MONDO:0022610", "names": ["bronchiectasis oligospermia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bronchiectasis oligospermia", "shortest_name_length": 27}
{"curie": "MONDO:0010795", "names": ["Oncocytoma", "oncocytoma", "Oncocytic Tumor", "oncocytic tumor", "oncocytic neoplasm", "oncocytoma, benign", "ONCOCYTOMA, BENIGN", "Oncocytic Neoplasm", "Papillary Thyroid Carcinoma, Oncocytic Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oncocytic neoplasm", "shortest_name_length": 10}
{"curie": "MONDO:0100490", "names": ["BNAH1", "Amazia", "amazia", "AMAZIA", "athelia", "ATHELIA", "AMASTIA", "Amastia", "amastia", "absent; nipple in amastia", "Isolated congenital amastia", "amastia; with absent nipple", "Congenital absent breast or nipple", "Isolated congenital breast hypoplasia/aplasia", "Congenital absence of breast with absent nipple", "absence; breast(s), congenital, with absent nipple", "breast(s); absence, congenital, with absent nipple", "breasts and/or nipples, aplasia or hypoplasia of, 1", "BREASTS AND/OR NIPPLES, APLASIA OR HYPOPLASIA OF, 1", "Congenital absence of breast with absent nipple (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breasts and/or nipples, aplasia or hypoplasia of, 1", "shortest_name_length": 5}
{"curie": "UMLS:C1334605", "names": ["Malignant Minor Salivary Gland Mixed Tumor", "Malignant Minor Salivary Gland Mixed Neoplasm", "Malignant Mixed Tumor of Minor Salivary Gland", "Malignant Mixed Neoplasm of Minor Salivary Gland", "Malignant Mixed Tumor of the Minor Salivary Gland", "Malignant Mixed Neoplasm of the Minor Salivary Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Mixed Tumor of the Minor Salivary Gland", "shortest_name_length": 42}
{"curie": "MONDO:0015978", "names": ["neutrophilopathy", "neutrophil disease", "neutrophil disorder", "disorders neutrophil", "Neutrophilic disorder", "neutrophils disorders", "neutrophilic disorder", "disorders neutrophilic", "Disorder of neutrophils", "disorder of neutrophils", "DISORDERS OF NEUTROPHILS", "functional neutrophil defect", "Disorder of neutrophils (disorder)", "disorder of neutrophils (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "functional neutrophil defect", "shortest_name_length": 16}
{"curie": "MONDO:0014847", "names": ["SPGF15", "SYCE1 azoospermia", "SPERMATOGENIC FAILURE 15", "spermatogenic failure 15", "spermatogenic failure type 15", "spermatogenic failure 15; SPGF15", "azoospermia caused by mutation in SYCE1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 15", "shortest_name_length": 6}
{"curie": "MONDO:0005023", "names": ["dci", "dcis", "DCIS", "DCIS, NOS", "DCIS of the breast", "carcinoma intraductal", "intraductal carcinoma", "carcinoma ductal situ", "ductal carcinoma situ", "Intraductal carcinoma", "Intraductal Carcinoma", "Intraductal Carcinomas", "Carcinoma, Intraductal", "Carcinomas, Intraductal", "carcinoma ductal in situ", "ductal in situ carcinoma", "ductal carcinoma in situ", "Ductal carcinoma in situ", "Ductal Carcinoma In Situ", "in situ ductal carcinoma", "intraductal breast cancer", "breast cancer intraductal", "Intraductal carcinoma, NOS", "Intraduct carcinoma in-situ", "Intraductal Breast Carcinoma", "breast carcinoma ductal situ", "intraductal breast carcinoma", "intraductal carcinoma breast", "Intraductal carcinoma in situ", "breast; intraductal carcinoma", "Intraduct carcinoma of breast", "intraductal; carcinoma, breast", "breast; carcinoma, intraductal", "mammary duct carcinoma in situ", "mammary duct in situ carcinoma", "carcinoma; intraductal, breast", "stage 0 mammary duct carcinoma", "Intraductal Carcinoma of Breast", "Ductal Carcinoma In Situ (DCIS)", "ductal carcinoma in situ (DCIS)", "in situ ductal breast carcinoma", "ductal breast carcinoma in situ", "Intraductal carcinoma of breast", "DCIS - ductal carcinoma in situ", "intraductal carcinoma of breast", "Ductal Breast Carcinoma In Situ", "Breast Ductal Carcinoma In Situ", "breast ductal carcinoma in situ", "carcinoma in situ of mammary duct", "Carcinoma in situ of breast ductal", "ductal carcinoma in situ of breast", "Ductal intraepithelial neoplasia 3", "Ductal Carcinoma In Situ of Breast", "Ductal Carcinoma in situ of Breast", "Intraductal Carcinoma of the Breast", "ductal cancer in situ of the breast", "intraductal carcinoma of the breast", "Breast Ductal Carcinoma In Situ, NOS", "non-invasive ductal breast carcinoma", "Non-Invasive Ductal Breast Carcinoma", "breast; intraductal carcinoma in situ", "Intraductal carcinoma noninfiltrating", "Noninfiltrating Intraductal Carcinoma", "Non-infiltrating intraductal carcinoma", "non-infiltrating intraductal carcinoma", "intraductal; carcinoma in situ, breast", "Carcinoma, Noninfiltrating Intraductal", "Intraductal Carcinoma, Noninfiltrating", "carcinoma in situ; intraductal, breast", "Ductal Carcinoma In Situ of the Breast", "breast malignant carcinoma intraductal", "Non-Infiltrating Intraductal Carcinoma", "ductal carcinoma in situ of the breast", "Noninfiltrating Intraductal Carcinomas", "breast; carcinoma in situ, intraductal", "non-invasive ductal carcinoma of breast", "Intraductal carcinoma in situ of breast", "Intraductal Carcinomas, Noninfiltrating", "Non-Invasive Ductal Carcinoma of Breast", "Intraductal carcinoma, non-infiltrating", "Carcinoma, Intraductal, Noninfiltrating", "Carcinomas, Noninfiltrating Intraductal", "carcinoma; intraductal, unspecified site", "Non-Infiltrating Ductal Breast Carcinoma", "intraductal; carcinoma, unspecified site", "non-infiltrating ductal breast carcinoma", "Non-Invasive Ductal Breast Adenocarcinoma", "non-invasive ductal breast adenocarcinoma", "Intraductal carcinoma, noninfiltrating NOS", "DIN 3 - ductal intraepithelial neoplasia 3", "Intraductal carcinoma, noninfiltrating, NOS", "Non-Infiltrating Ductal Carcinoma of Breast", "non-invasive ductal carcinoma of the breast", "Non-infiltrating intraductal adenocarcinoma", "Non-Infiltrating Intraductal Adenocarcinoma", "non-infiltrating ductal carcinoma of breast", "Intraductal carcinoma of breast (diagnosis)", "Non-Invasive Ductal Carcinoma of the Breast", "non-infiltrating intraductal adenocarcinoma", "Intraductal adenocarcinoma, non-infiltrating", "non-invasive ductal adenocarcinoma of breast", "Non-Invasive Ductal Adenocarcinoma of Breast", "non-infiltrating ductal breast adenocarcinoma", "Non-Infiltrating Ductal Breast Adenocarcinoma", "breast neoplasm carcinoma in situ intraductal", "Non-Invasive Intraductal Breast Adenocarcinoma", "non-invasive intraductal breast adenocarcinoma", "non-infiltrating ductal carcinoma of the breast", "Breast cancer - ductal carcinoma in situ (DCIS)", "Non-Infiltrating Ductal Carcinoma of the Breast", "Intraductal adenocarcinoma, noninfiltrating, NOS", "Non-Invasive Ductal Adenocarcinoma of the Breast", "non-invasive ductal adenocarcinoma of the breast", "Non-Infiltrating Ductal Adenocarcinoma of Breast", "intraductal; carcinoma in situ, unspecified site", "carcinoma in situ; intraductal, unspecified site", "non-infiltrating ductal adenocarcinoma of breast", "Non-Invasive Intraductal Adenocarcinoma of Breast", "non-invasive intraductal adenocarcinoma of breast", "Non-Infiltrating Intraductal Breast Adenocarcinoma", "Intraductal carcinoma in situ of breast (disorder)", "non-infiltrating intraductal breast adenocarcinoma", "Intraductal carcinoma in situ of breast (diagnosis)", "non-infiltrating ductal adenocarcinoma of the breast", "adenocarcinoma; intraductal, noninfiltrating, breast", "Non-Infiltrating Ductal Adenocarcinoma of the Breast", "non-invasive intraductal adenocarcinoma of the breast", "non-infiltrating intraductal adenocarcinoma of breast", "Non-Invasive Intraductal Adenocarcinoma of the Breast", "Non-Infiltrating Intraductal Adenocarcinoma of Breast", "Breast Ductal Carcinoma In Situ, Not Otherwise Specified", "Non-Infiltrating Intraductal Adenocarcinoma of the Breast", "non-infiltrating intraductal adenocarcinoma of the breast", "Non-infiltrating intraductal carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ductal breast carcinoma in situ", "shortest_name_length": 3}
{"curie": "UMLS:C3272425", "names": ["Gastric Schwannoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Schwannoma", "shortest_name_length": 18}
{"curie": "MONDO:0042724", "names": ["Volcke Soekarman syndrome", "macrocephaly, intellectual disability, short stature, spastic paraplegia and cns malformations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macrocephaly, intellectual disability, short stature, spastic paraplegia and cns malformations", "shortest_name_length": 25}
{"curie": "UMLS:C5670672", "names": ["Stage IB Cervical Cancer FIGO 2009", "Stage IB Cervical Carcinoma FIGO 2009"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Cervical Cancer FIGO 2009", "shortest_name_length": 34}
{"curie": "UMLS:C1096280", "names": ["Aqueous fibrin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aqueous fibrin", "shortest_name_length": 14}
{"curie": "MONDO:0008314", "names": ["Pronation-Supination Of The Forearm, Impairment Of", "PRONATION-SUPINATION OF THE FOREARM, IMPAIRMENT OF", "pronation-supination of the forearm, impairment of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pronation-supination of the forearm, impairment of", "shortest_name_length": 50}
{"curie": "UMLS:C0854382", "names": ["Libido disorder", "Libido disorder NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Libido disorder", "shortest_name_length": 15}
{"curie": "MONDO:0100045", "names": ["EV1", "epidermodysplasia verruciformis 1", "EPIDERMODYSPLASIA VERRUCIFORMIS, SUSCEPTIBILITY TO, 1", "epidermodysplasia verruciformis, susceptibility to, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermodysplasia verruciformis, susceptibility to, 1", "shortest_name_length": 3}
{"curie": "UMLS:C5205726", "names": ["Prostate Intraductal Carcinoma", "Intraductal Prostate Carcinoma", "Intraductal carcinoma of prostate", "Intraductal Prostate Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraductal Prostate Carcinoma", "shortest_name_length": 30}
{"curie": "UMLS:C0206762", "names": ["LIMB MALFORMATION", "Limb malformation", "limb malformation", "limb malformations", "Limb malformations", "limbs malformation", "Limb malformation NOS", "LIMB ANOMALY CONGENITAL", "Congenital Limb Deformity", "Deformity, Congenital Limb", "Limb Deformity, Congenital", "Congenital anomaly of limb", "Congenital limb anomaly NOS", "Congenital Limb Deformities", "Congenital deformity of limb", "Deformities, Congenital Limb", "Limb Deformities, Congenital", "Congenital limb malformation", "CONGENITAL ABNORMALITY OF LIMB", "congenital malformation of limb", "Congenital deformities of limbs", "Congenital anomaly of limb, NOS", "Congenital limb malformation NOS", "Congenital deformity of limb, NOS", "CONGENITAL ANOMALIES OF THE LIMBS", "Congenital anomaly of limb(s) NOS", "Congenital abnormality of the limb", "Congenital anomaly of limb (disorder)", "Unspecified anomaly of unspecified limb", "Congenital anomaly NOS of unspecified limb", "congenital malformation of limb (diagnosis)", "Congenital deformity NOS of unspecified limb", "Unspecified congenital malformation of limb(s)", "Unspecified congenital anomaly of unspecified limb"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Limb Deformities, Congenital", "shortest_name_length": 17}
{"curie": "UMLS:C3542021", "names": ["Duchenne Becker Muscular Dystrophy", "Duchenne-Becker Muscular Dystrophy", "Muscular Dystrophy, Duchenne-Becker", "Duchenne and Becker muscular dystrophy", "Duchenne and Becker Muscular Dystrophy", "Muscular Dystrophy, Duchenne and Becker Types", "Severe dystrophinopathy, Duchenne and Becker type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Duchenne and Becker Muscular Dystrophy", "shortest_name_length": 34}
{"curie": "UMLS:C1519369", "names": ["Anaplastic Large Cell Lymphoma, Sarcomatoid Subtype"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anaplastic Large Cell Lymphoma, Sarcomatoid Subtype", "shortest_name_length": 51}
{"curie": "UMLS:C0262385", "names": ["Autonomic imbalance", "autonomic imbalance", "imbalance; autonomic", "autonomic; imbalance", "Autonomic instability", "AUTONOMIC INSTABILITY", "autonomic instability", "Autonomic nervous system imbalance", "IMBALANCE AUTONOMIC NERVOUS SYSTEM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Autonomic nervous system imbalance", "shortest_name_length": 19}
{"curie": "UMLS:C0038992", "names": ["Miliary fever", "fever sweating", "Sweating fever", "Sweating Fever", "sweating fever", "Sweating disease", "disease sweating", "diseases sweating", "Sweating fever (finding)", "sweating fever (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sweating fever", "shortest_name_length": 13}
{"curie": "UMLS:C1697918", "names": ["Metastatic Breast Adenocarcinoma", "Breast adenocarcinoma metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast adenocarcinoma metastatic", "shortest_name_length": 32}
{"curie": "UMLS:C5555129", "names": ["Refractory Aggressive T-Cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Aggressive T-Cell Non-Hodgkin Lymphoma", "shortest_name_length": 49}
{"curie": "MONDO:0030997", "names": ["MC1DN37", "mitochondrial complex I deficiency, nuclear type 37", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 37", "mitochondrial complex 1 deficiency, nuclear type 37"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 37", "shortest_name_length": 7}
{"curie": "UMLS:C5446663", "names": ["Metastatic Malignant Glomus Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Malignant Glomus Tumor", "shortest_name_length": 33}
{"curie": "MONDO:0002108", "names": ["thyroid ca", "Thyroid Ca", "THYROID CANCER", "thyroid cancer", "Thyroid cancer", "thyroid cancers", "thyroid neoplasm", "Cancer of thyroid", "Thyroid gland cancer", "thyroid gland cancer", "cancer of the thyroid", "thyroid gland neoplasm", "Thyroid gland neoplasm", "Malignant Thyroid Tumor", "cancer of thyroid gland", "malignant thyroid tumor", "neoplasm of thyroid gland", "Malignant neoplasm thyroid", "Thyroid neoplasm malignant", "THYROID NEOPLASM MALIGNANT", "malignant thyroid neoplasm", "Malignant Thyroid Neoplasm", "Malignant Tumor of Thyroid", "malignant tumor of thyroid", "Thyroid neoplasms malignant", "Neoplasm malig;thyroid gland", "malignant thyroid gland tumor", "Malignant Neoplasm of Thyroid", "Malignant neoplasm of thyroid", "malignant neoplasm of thyroid", "Malignant Thyroid Gland Tumor", "malignant tumor of the thyroid", "Malignant Tumor of the Thyroid", "malignant thyroid gland neoplasm", "Malignant Thyroid Gland Neoplasm", "malignant tumor of thyroid gland", "Malignant Tumor of Thyroid Gland", "Malignant tumor of thyroid gland", "malignant neoplasm of the thyroid", "Malignant Neoplasm of the Thyroid", "malignant tumour of thyroid gland", "Malignant tumour of thyroid gland", "Malignant neoplasm of thyroid gland", "malignant neoplasm of thyroid gland", "Malignant Neoplasm of Thyroid Gland", "malignant tumor of the thyroid gland", "Malignant Tumor of the Thyroid Gland", "Malignant Neoplasm of the Thyroid Gland", "malignant neoplasm of the thyroid gland", "malignant neosplasm of the thyroid gland", "Malignant tumor of thyroid gland (disorder)", "malignant neoplasm of thyroid gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid cancer", "shortest_name_length": 10}
{"curie": "UMLS:C0854844", "names": ["Intestinal T-Cell Lymphoma Refractory", "Intestinal T-cell lymphoma refractory", "Refractory Intestinal T-Cell Lymphoma", "Refractory Enteropathy-Associated T-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal T-cell lymphoma refractory", "shortest_name_length": 37}
{"curie": "UMLS:C4054539", "names": ["Malignancy Associate Membranous Nephropathy", "Membranous Nephropathy - Malignancy Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Membranous Nephropathy - Malignancy Associated", "shortest_name_length": 43}
{"curie": "UMLS:C0741292", "names": ["atrial flutter paroxysmal", "paroxysmal atrial flutter", "ATRIAL FLUTTER PAROXYSMAL", "Paroxysmal atrial flutter", "Flutter;atrial;paroxysmal", "Atrial flutter, paroxysmal", "Paroxysmal atrial flutter (disorder)", "Paroxysmal atrial flutter (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paroxysmal atrial flutter", "shortest_name_length": 25}
{"curie": "UMLS:C2981417", "names": ["Stage IIIA Small Intestinal Gastrointestinal Stromal Tumor", "Stage IIIA Small Intestinal Gastrointestinal Stromal Tumor (GIST)", "Stage IIIA Small Intestinal Gastrointestinal Stromal Tumor AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Small Intestinal Gastrointestinal Stromal Tumor", "shortest_name_length": 58}
{"curie": "UMLS:C4727090", "names": ["Locally Advanced Lung Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Lung Carcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C3203553", "names": ["Maternal preconception exposure", "Maternal exposure before pregnancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Maternal exposure before pregnancy", "shortest_name_length": 31}
{"curie": "MONDO:0002405", "names": ["Liver Vascular Disorder", "liver vascular disorder", "hepatic vascular disease", "Hepatic Vascular Disorder", "Hepatic vascular disorder", "hepatic vascular disorder", "Hepatic vascular disorders", "vascular disorder of liver", "Vascular disorder of liver", "Vascular disorder of liver (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatic vascular disorder", "shortest_name_length": 23}
{"curie": "UMLS:C1511311", "names": ["Breast Follicular Lymphoma", "follicular malignant lymphoma of breast", "follicular malignant lymphoma of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "follicular malignant lymphoma of breast", "shortest_name_length": 26}
{"curie": "UMLS:C5420439", "names": ["Maxillofacial Osteoid Osteoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Maxillofacial Osteoid Osteoma", "shortest_name_length": 29}
{"curie": "MONDO:0800034", "names": ["MTTH MELAS syndrome", "MELAS syndrome caused by mutation in MTTH"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MELAS syndrome caused by mutation in MTTH", "shortest_name_length": 19}
{"curie": "UMLS:C0473218", "names": ["Ischemic glomerulopathy", "glomerulopathy ischemic", "Ischemic Glomerulopathy", "Ischaemic glomerulopathy", "diffuse glomerulosclerosis", "Diffuse glomerulosclerosis", "Glomerulopathy due to ischemia", "Glomerulopathy due to ischaemia", "Ischemic glomerulopathy (diagnosis)", "Glomerulopathy due to ischemia (disorder)", "Diffuse glomerulosclerosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse glomerulosclerosis", "shortest_name_length": 23}
{"curie": "MONDO:0011372", "names": ["microcephaly with simplified gyral pattern", "Microcephaly with simplified gyral pattern", "Microcephaly with Simplified Gyral Pattern", "MICROCEPHALY WITH SIMPLIFIED GYRAL PATTERN", "Microcephaly with simplified gyral pattern (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly with simplified gyral pattern", "shortest_name_length": 42}
{"curie": "UMLS:C5238347", "names": ["BRCA-Mutated Breast Carcinoma", "BRCA-Associated Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "BRCA-Associated Breast Carcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0024412", "names": ["Peptostreptococcus infection", "Peptostreptococcus infectious disease", "Peptostreptococcus disease or disorder", "Peptostreptococcus infection (disorder)", "Peptostreptococcus caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peptostreptococcus infectious disease", "shortest_name_length": 28}
{"curie": "MONDO:0021856", "names": ["Alsing syndrome", "atypical macular coloboma, familial juvenile nephronophthisis and skeletal abnormality"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alsing syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0013343", "names": ["C1QD", "C1Q DEFICIENCY", "C1q Deficiency", "C1q deficiency", "C1Q deficiency", "C1q DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "C1Q deficiency", "shortest_name_length": 4}
{"curie": "UMLS:C2931329", "names": ["Microdeletion 22 q11", "Chromosome 22, microdeletion 22 q11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chromosome 22, microdeletion 22 q11", "shortest_name_length": 20}
{"curie": "MONDO:0001284", "names": ["endometriosis; bowel", "bowel; endometriosis", "endometriosis intestine", "intestinal endometriosis", "endometriosis intestines", "endometriosis of intestine", "Endometriosis of intestine", "Endometriosis of intestine, NOS", "intestine endometriosis (disease)", "endometriosis (disease) of intestine", "Endometriosis of intestine (disorder)", "endometriosis of intestine (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometriosis of intestine", "shortest_name_length": 20}
{"curie": "UMLS:C0521647", "names": ["Neonatal apneic attack", "Neonatal Apneic Attack", "Neonatal apnoeic attack", "Neonatal apneic attack (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neonatal apneic attack", "shortest_name_length": 22}
{"curie": "UMLS:C4683560", "names": ["Mycosis Fungoides by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mycosis Fungoides by AJCC v7 Stage", "shortest_name_length": 34}
{"curie": "MONDO:0024661", "names": ["Tubulovillous adenoma", "Tubulovillous Adenoma", "tubulovillous adenoma", "ADENOMA TUBULOVILLOUS", "Villoglandular adenoma", "adenomas tubulovillous", "Papillotubular adenoma", "Tubulo-papillary adenoma", "Tubulovillous adenoma NOS", "Tubulovillous adenoma, NOS", "GI Tract Tubulovillous Adenoma", "Gastrointestinal Tract Tubulovillous Adenoma", "Tubulovillous adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tubulovillous adenoma", "shortest_name_length": 21}
{"curie": "MONDO:0011918", "names": ["angst", "Angst", "Anxious", "anxiety", "Anxiety", "ANXIETY", "anxious", "anxieties", "anxiousness", "Anxiousness", "RNDx anxiety", "Feel anxious", "harm avoidance", "Feeling;anxious", "Feeling anxious", "feeling anxious", "Anxiety disease", "anxiety reaction", "REACTION ANXIETY", "Anxious behavior", "Anxiety reaction", "ANXIETY REACTION", "Reaction anxiety", "Anxiety Reaction", "Anxiety (finding)", "unfocused anxiety", "anxious; sensation", "RNDx anxiety (diagnosis)", "anxiety-related personality traits", "Excessive, persistent worry and fear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anxiety", "shortest_name_length": 5}
{"curie": "MONDO:0008567", "names": ["NMTC1", "papillary carcinoma of thyroid", "thyroid cancer, nonmedullary, 1", "THYROID CANCER, NONMEDULLARY, 1", "Familial Nonmedullary Thyroid Cancer", "thyroid cancer, nonmedullary, type 1", "nonmedullary thyroid carcinoma, papillary", "FAMILIAL NONMEDULLARY THYROID CANCER, PAPILLARY", "familial nonmedullary thyroid cancer, papillary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid cancer, nonmedullary, 1", "shortest_name_length": 5}
{"curie": "MONDO:0014500", "names": ["CCDD", "atrial conduction disease", "CARDIAC conduction disease with or without dilated cardiomyopathy", "CARDIAC CONDUCTION DISEASE WITH OR WITHOUT DILATED CARDIOMYOPATHY", "familial atrial tachyarrhythmia-infra-Hisian cardiac conduction disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial conduction disease", "shortest_name_length": 4}
{"curie": "UMLS:C5418967", "names": ["Parietal Lobe Anaplastic Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parietal Lobe Anaplastic Astrocytoma", "shortest_name_length": 36}
{"curie": "MONDO:0022831", "names": ["congenital heart disease ptosis hypodontia craniostosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital heart disease ptosis hypodontia craniostosis", "shortest_name_length": 55}
{"curie": "MONDO:0009455", "names": ["IMMUNODEFICIENCY, PARTIAL COMBINED, WITH ABSENCE OF HLA DETERMINANTS AND BETA-2-MICROGLOBULIN FROM LYMPHOCYTES", "Immunodeficiency, Partial Combined, with Absence of HLA Determinants and Beta-2-Microglobulin from Lymphocytes", "immunodeficiency, partial combined, with absence of HLA Determinants and beta-2-microglobulin from lymphocytes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency, partial combined, with absence of HLA Determinants and beta-2-microglobulin from lymphocytes", "shortest_name_length": 110}
{"curie": "UMLS:C5239295", "names": ["Locally Advanced Renal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Renal Cell Carcinoma", "shortest_name_length": 37}
{"curie": "UMLS:C0343970", "names": ["Hepatic schistosomal granuloma", "Hepatic Schistosomal Granuloma", "Hepatic schistosomal granuloma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatic schistosomal granuloma", "shortest_name_length": 30}
{"curie": "UMLS:C3641147", "names": ["Fetal Neurodevelopmental Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fetal Neurodevelopmental Disorder", "shortest_name_length": 33}
{"curie": "MONDO:0006506", "names": ["HNSHA", "Hereditary nonspherocytic hemolytic anemia", "congenital nonspherocytic hemolytic anemia", "hereditary nonspherocytic hemolytic anemia", "Congenital nonspherocytic hemolytic anemia", "Congenital Nonspherocytic Hemolytic Anemia", "congenital nonspherocytic hemolytic anaemia", "Hemolytic Anemia, Congenital Nonspherocytic", "hereditary nonspherocytic hemolytic anaemia", "Anemia, Congenital Nonspherocytic Hemolytic", "Congenital non-spherocytic hemolytic anemia", "Anemia, Hemolytic Congenital, Nonspherocytic", "Hereditary nonspherocytic haemolytic anaemia", "Congenital nonspherocytic haemolytic anaemia", "Anemia, Hemolytic, Congenital Nonspherocytic", "Hereditary nonspherocytic hemolytic anemia, NOS", "Congenital nonspherocytic hemolytic anemia, NOS", "Hereditary nonspherocytic haemolytic anaemia, NOS", "Congenital nonspherocytic haemolytic anaemia, NOS", "Hereditary nonspherocytic hemolytic anemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital nonspherocytic hemolytic anemia", "shortest_name_length": 5}
{"curie": "MONDO:0005944", "names": ["Rhabdovirus infection", "Rhabdoviridae infection", "Rhabdoviridae Infection", "Rhabdoviridae Infections", "infection, Rhabdoviridae", "Infection, Rhabdoviridae", "infections, Rhabdoviridae", "Infections, Rhabdoviridae", "Rhabdovirus infection, NOS", "Disease due to Rhabdoviridae", "DISEASES DUE TO RHABDOVIRIDAE", "Disease caused by Rhabdoviridae", "Rhabdoviridae infectious disease", "Disease due to Rhabdoviridae, NOS", "Disease caused by Rhabdoviridae (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rhabdoviridae infectious disease", "shortest_name_length": 21}
{"curie": "UMLS:C4687714", "names": ["Steroid Refractory GVHD", "Steroid Refractory cGVHD", "Steroid Refractory Graft Versus Host Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Steroid Refractory Graft Versus Host Disease", "shortest_name_length": 23}
{"curie": "UMLS:C0393699", "names": ["Symptomatic West syndrome", "Symptomatic West Syndrome", "Syndrome, Symptomatic West", "West Syndrome, Symptomatic", "Symptomatic Infantile Spasm", "Spasm, Symptomatic Infantile", "Symptomatic Infantile Spasms", "Infantile Spasm, Symptomatic", "Infantile Spasms, Symptomatic", "Spasms, Symptomatic Infantile", "Symptomatic West syndrome (disorder)", "Symptomatic West syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Symptomatic Infantile Spasms", "shortest_name_length": 25}
{"curie": "UMLS:C3839955", "names": ["Malignant Ossifying Fibromyxoid Tumor", "Ossifying fibromyxoid tumor, malignant", "Ossifying fibromyxoid tumour, malignant", "Ossifying fibromyxoid tumor, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ossifying fibromyxoid tumor, malignant", "shortest_name_length": 37}
{"curie": "MONDO:0030048", "names": ["HARPO", "Harderoporphyria", "HARDEROPORPHYRIA", "harderoporphyria", "Homozygous hereditary coproporphyria", "Homozygous hereditary coproporphyria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "harderoporphyria", "shortest_name_length": 5}
{"curie": "MONDO:0002087", "names": ["cancer peritoneal", "peritoneum cancer", "cancer peritoneum", "Peritoneal Cancer", "peritoneal cancer", "Peritoneal cancer", "Peritoneum--Cancer", "peritoneal neoplasm", "Cancer of Peritoneum", "cancer of peritoneum", "Cancer of peritoneum", "Peritoneal Cavity Cancer", "Cancer of the Peritoneum", "peritoneal cavity cancer", "cancer of the peritoneum", "CA - Cancer of peritoneum", "malignant peritoneal neoplasm", "Malignant peritoneal neoplasm", "Malignant tumor of peritoneum", "Malignant Peritoneal Neoplasm", "malignant peritoneum neoplasm", "malignant tumor of peritoneum", "Malignant tumour of peritoneum", "Primary peritoneal cavity cancer", "malignant neoplasm of peritoneum", "primary peritoneal cavity cancer", "Malignant peritoneal neoplasm NOS", "Malignant tumor of peritoneum (disorder)", "Malignant neoplasm of the peritoneum, NOS", "malignant neoplasm of peritoneum (diagnosis)", "Malignant neoplasm of peritoneum, unspecified", "peritoneal neoplasm malignant of specified parts", "Malignant neoplasm of specified parts of peritoneum", "malignant neoplasm of specified parts of peritoneum", "malignant neoplasm of specified parts of peritoneum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peritoneum cancer", "shortest_name_length": 17}
{"curie": "MONDO:0017350", "names": ["metabolic disorder; tryptophan", "tryptophan; metabolic disorder", "Tryptophan Metabolism Alterations", "Disorder of tryptophan metabolism", "disorder of tryptophan metabolism", "Disorders of tryptophan metabolism", "DISORDERS OF TRYPTOPHAN METABOLISM", "Disorder of tryptophan metabolism, NOS", "inborn disorder of tryptophan metabolism", "Disorder of tryptophan metabolism (disorder)", "inborn error of tryptophan metabolic process", "inborn tryptophan metabolic process disorder", "rare inborn error of tryptophan metabolic process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of tryptophan metabolism", "shortest_name_length": 30}
{"curie": "UMLS:C1275325", "names": ["primary cutaneous diffuse large B-cell lymphoma", "Primary Cutaneous Diffuse Large B-Cell Lymphoma", "Primary cutaneous diffuse large cell B-cell lymphoma", "primary cutaneous diffuse large B-cell lymphoma (diagnosis)", "Primary cutaneous diffuse large cell B-cell lymphoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary cutaneous diffuse large cell B-cell lymphoma", "shortest_name_length": 47}
{"curie": "MONDO:0014591", "names": ["DRS2", "autosomal dominant Robinow syndrome 2", "ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2", "Robinow syndrome, autosomal dominant 2", "DVL1 autosomal dominant Robinow syndrome", "autosomal dominant Robinow syndrome type 2", "Robinow syndrome, autosomal dominant type 2", "autosomal dominant Robinow syndrome caused by mutation in DVL1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant Robinow syndrome 2", "shortest_name_length": 4}
{"curie": "UMLS:C4053528", "names": ["CRINET", "Cribriform Neuroepithelial Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cribriform Neuroepithelial Tumor", "shortest_name_length": 6}
{"curie": "UMLS:C0280350", "names": ["Stage II Mouth Verrucous Carcinoma", "Stage II Verrucous Carcinoma of Mouth", "Stage II Oral Cavity Verrucous Cancer", "Stage II Oral Cavity Verrucous Carcinoma", "oral cavity verrucous carcinoma, stage II", "Stage II Verrucous Carcinoma of the Mouth", "Stage II Verrucous Carcinoma of Oral Cavity", "Verrucous carcinoma of the oral cavity stage II", "stage II verrucous carcinoma of the oral cavity", "Stage II Verrucous Carcinoma of the Oral Cavity", "verrucous carcinoma of the oral cavity, stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Verrucous carcinoma of the oral cavity stage II", "shortest_name_length": 34}
{"curie": "UMLS:C5670579", "names": ["Refractory Transformed Indolent B-Cell Non-Hodgkin Lymphoma to Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Transformed Indolent B-Cell Non-Hodgkin Lymphoma to Diffuse Large B-Cell Lymphoma", "shortest_name_length": 92}
{"curie": "MONDO:0009069", "names": ["LSFC", "MC4DN5", "SLSJ-COX deficiency", "French Canadian Leigh disease", "Leigh syndrome French-Canadian type", "French Canadian type Leigh syndrome", "French Canadian type COX deficiency", "Leigh syndrome, French-Canadian type", "LEIGH SYNDROME, FRENCH CANADIAN TYPE", "Cox deficiency, French Canadian type", "Cox Deficiency, French-Canadian Type", "COX DEFICIENCY, FRENCH CANADIAN TYPE", "COX deficiency, French-Canadian type", "Leigh syndrome, French Canadian type", "Leigh Syndrome, French-Canadian Type", "Leigh syndrome , French Canadian type", "Saguenay Lac saint Jean type COX deficiency", "Saguenay Lac saint Jean type Leigh syndrome", "Cox deficiency, Saguenay Lac saint Jean type", "LEIGH SYNDROME, SAGUENAY-LAC-SAINT-JEAN TYPE", "COX DEFICIENCY, SAGUENAY-LAC-SAINT-JEAN TYPE", "Leigh syndrome, Saguenay-Lac-Saint-Jean type", "Leigh Syndrome, Saguenay-Lac Saint-Jean Type", "Leigh syndrome, Saguenay Lac saint Jean type", "Cox deficiency, Saguenay-Lac-Saint-Jean type", "Cox Deficiency, Saguenay-Lac Saint-Jean Type", "MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 5", "French Canadian type cytochrome c oxidase deficiency", "Cytochrome C oxidase deficiency French-Canadian type", "Cytochrome c oxidase deficiency, French Canadian type", "Cytochrome C oxidase deficiency, French-Canadian type", "cytochrome C oxidase deficiency, French-Canadian type", "cytochrome C oxidase deficiency, French Canadian type", "Cytochrome C Oxidase Deficiency, French-Canadian Type", "CYTOCHROME c OXIDASE DEFICIENCY, FRENCH CANADIAN TYPE", "Congenital lactic acidosis Saguenay-Lac-Saint-Jean type", "Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type", "congenital lactic acidosis, Saguenay-Lac-Saint-Jean type", "Cytochrome oxidase deficiency Saguenay-Lac-Saint-Jean type", "Cytochrome oxidase deficiency, Saguenay-Lac-Saint-Jean type", "cytochrome oxidase deficiency, Saguenay-Lac-Saint-Jean type", "Congenital lactic acidosis Saguenay-Lac-Saint-Jean type (disorder)", "mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital lactic acidosis, Saguenay-Lac-Saint-Jean type", "shortest_name_length": 4}
{"curie": "UMLS:C1336705", "names": ["Carcinoid Tumor of Testis", "Testicular Carcinoid Tumor", "Carcinoid Tumor of the Testis", "Testicular Neuroendocrine Tumor G1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular Neuroendocrine Tumor G1", "shortest_name_length": 25}
{"curie": "UMLS:C0302858", "names": ["protein-losing gastroenteropathy", "protein losing gastroenteropathy", "Protein-losing gastroenteropathy", "gastroenteropathy, protein losing", "GASTROENTEROPATHY, PROTEIN-LOSING"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Protein-losing gastroenteropathy", "shortest_name_length": 32}
{"curie": "MONDO:0011727", "names": ["AN", "anon", "ANON", "ANON1", "ANOREXIA NERVOSA, SUSCEPTIBILITY TO", "anorexia nervosa, susceptibility to", "ANOREXIA NERVOSA, SUSCEPTIBILITY TO, 1", "anorexia nervosa, susceptibility to, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anorexia nervosa, susceptibility to, 1", "shortest_name_length": 2}
{"curie": "MONDO:0011280", "names": ["SCZD6", "SCHIZOPHRENIA 6", "schizophrenia 6", "schizophrenia susceptibility locus, chromosome 8P-related", "SCHIZOPHRENIA SUSCEPTIBILITY LOCUS, CHROMOSOME 8p-RELATED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schizophrenia 6", "shortest_name_length": 5}
{"curie": "MONDO:0004538", "names": ["cervical adenocarcinoma, endocervical type", "Mucinous adenocarcinoma, endocervical type", "endocervical type cervical mucinous adenocarcinoma", "Cervical Mucinous Adenocarcinoma, Endocervical-Type", "cervical mucinous adenocarcinoma, endocervical type", "Cervical Mucinous Adenocarcinoma, Endocervical Type", "Mucinous adenocarcinoma, endocervical type (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endocervical type cervical mucinous adenocarcinoma", "shortest_name_length": 42}
{"curie": "UMLS:C4055487", "names": ["Adult Extracardiac Rhabdomyoma", "Adult Extracardiac Rhabdomyomatous Hamartoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Extracardiac Rhabdomyoma", "shortest_name_length": 30}
{"curie": "MONDO:0016003", "names": ["Erlichiosis", "erlichiosis", "EHRLICHIOSES", "Ehrlichiosis", "ehrlichioses", "Ehrlichioses", "EHRLICHIOSIS", "ehrlichiosis", "Ehrlichiosis, NOS", "Human ehrlichiosis", "human ehrlichiosis", "Human Ehrlichioses", "Human Ehrlichiosis", "Ehrlichia Infection", "Ehrlichia Infections", "ehrlichiosis (diagnosis)", "Ehrlichiosis, unspecified", "Human ehrlichiosis (disorder)", "tick-borne rickettsiosis ehrlichiosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ehrlichiosis", "shortest_name_length": 11}
{"curie": "UMLS:C1336179", "names": ["Stage IIB Endometrial Cancer AJCC v6", "Stage IIB Uterine Corpus Cancer AJCC v6", "Stage IIB Uterine (including Endometrial) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Uterine Corpus Cancer AJCC v6", "shortest_name_length": 36}
{"curie": "MONDO:0006314", "names": ["NOSE POLYP", "nose polyp", "NOSE, POLYP", "nasal polyp", "polyp nasal", "nose; polyp", "Nasal Polyp", "NASAL POLYP", "nose polyps", "polyp; nose", "Nasal polyp", "Polyp, Nasal", "Nasal polyps", "Nasal Polyps", "nasal polyps", "POLYPS NASAL", "Polyps nasal", "polyps nasal", "nasals polyps", "Polyps, Nasal", "Polyposis nasi", "Polyps of nose", "Polyp(s);nasal", "NASAL POLYPOSIS", "Nasal polyposis", "Nasal polyp NOS", "nasal polyposis", "polyposis nasal", "Nasal polyp, NOS", "nasal cavity polyp", "Nasal Cavity Polyp", "nasal cavity polyps", "polyp; nasal cavity", "nasal cavity; polyp", "cavity nasal polyps", "polyp of nasal cavity", "Polyp of nasal cavity", "Polyp of Nasal Cavity", "Nasal polyp - anterior", "Unspecified nasal polyp", "Polyp in anterior nares", "nasal polyps (diagnosis)", "Nasal polyp, unspecified", "polyp of the nasal cavity", "Polyp of the Nasal Cavity", "Polyp of nasal cavity, NOS", "nasal cavity polyps (diagnosis)", "Polyp of nasal cavity (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasal cavity polyp", "shortest_name_length": 10}
{"curie": "MONDO:0009206", "names": ["MCFD1", "FMFD1", "FMFD 1", "F5F8D1", "FMFD I", "FMFD syndrome, type I", "Factor V AND factor VIII deficiency", "Factor V and factor VIII deficiency", "combined factor V and VIII deficiency", "multiple coagulation Factor deficiency 1", "Multiple Coagulation Factor Deficiency I", "MULTIPLE COAGULATION FACTOR DEFICIENCY I", "Familial Multiple Coagulation Factor Deficiency I", "familial multiple coagulation Factor deficiency 1", "FAMILIAL MULTIPLE COAGULATION FACTOR DEFICIENCY I", "FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 1", "factor V and factor VIII, combined deficiency of, 1", "factor 5 and Factor VIII, combined deficiency of, 1", "Familial multiple factor deficiency syndrome, type I", "LMAN1 combined deficiency of factor V and factor VIII", "factor V and factor VIII, combined deficiency of, type 1", "Familial multiple factor deficiency syndrome, type I (disorder)", "combined deficiency of factor V and factor VIII caused by mutation in LMAN1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "factor V and factor VIII, combined deficiency of, type 1", "shortest_name_length": 5}
{"curie": "MONDO:0020371", "names": ["Essential iris atrophy", "essential iris atrophy", "Progressive iris atrophy", "progressive iris atrophy", "Essential iris atrophy (disorder)", "essential iris atrophy (diagnosis)", "progressive iris atrophy (diagnosis)", "Essential or progressive iris atrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "essential iris atrophy", "shortest_name_length": 22}
{"curie": "UMLS:C5206779", "names": ["Refractory Rhabdoid Tumor of the Kidney"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Rhabdoid Tumor of the Kidney", "shortest_name_length": 39}
{"curie": "MONDO:0032908", "names": ["MCTT", "CEBALID", "CEBALID SYNDROME", "CEBALID syndrome", "MN1 C-TERMINAL TRUNCATION SYNDROME", "MN1 C-terminal truncation syndrome", "CRANIOFACIAL DEFECTS, DYSMORPHIC EARS, STRUCTURAL BRAIN ABNORMALITIES, EXPRESSIVE LANGUAGE DELAY, AND IMPAIRED INTELLECTUAL DEVELOPMENT", "Craniofacial Defects, Dysmorphic Ears, Structural Brain Abnormalities, Expressive Language Delay, and Impaired Intellectual Development"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CEBALID syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0020529", "names": ["Hypersomnia with Periodic Respiration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypersomnia with Periodic Respiration", "shortest_name_length": 37}
{"curie": "MONDO:0020423", "names": ["coronary ostial stenosis or atresia", "stenosis or atresia of the coronary ostium", "stenosis or atrophy of the coronary ostium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stenosis or atrophy of the coronary ostium", "shortest_name_length": 35}
{"curie": "MONDO:0009742", "names": ["ELEJALDE disease", "Elejalde Disease", "Elejalde disease", "neuroectodermal melanolysosomal disease", "Melanolysosomal neurocutaneous syndrome", "Neuroectodermal melanolysosomal disease", "Neuro-ectodermal melanolysosomal syndrome", "Neuroectodermal melanolysosomal disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuroectodermal melanolysosomal disease", "shortest_name_length": 16}
{"curie": "UMLS:C0151836", "names": ["Paranoid reaction", "REACTION PARANOID", "paranoid reaction", "PARANOID REACTION", "Reaction paranoid", "reaction; paranoid", "paranoid; reaction", "Persecutory delusion", "persecution delusion", "persecutory delusions", "Persecutory delusions", "Paranoid reaction NOS", "Delusion of persecution", "delusions of persecution", "Delusion of persecution (finding)", "persecutory delusions (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paranoid reaction", "shortest_name_length": 17}
{"curie": "UMLS:C4744690", "names": ["Recurrent Adenovirus Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Adenovirus Infection", "shortest_name_length": 30}
{"curie": "UMLS:C0751174", "names": ["Juvenile Glycogen Storage Disease Type II", "Glycogen Storage Disease Type II, Juvenile"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Glycogen Storage Disease Type II, Juvenile", "shortest_name_length": 41}
{"curie": "UMLS:C0234972", "names": ["Disorder convulsive", "Convulsive disorder", "DISORDER CONVULSIVE", "Convulsion disorder", "CONVULSIVE DISORDER", "Convulsive Disorder", "CONVULSION DISORDER", "convulsive disorder", "convulsive disorders", "Convulsive disorder NOS", "convulsive disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Convulsive disorder", "shortest_name_length": 19}
{"curie": "UMLS:C0029925", "names": ["OVARIAN CARCINOMA", "Ovarian carcinoma", "Ovarian Carcinoma", "carcinoma of ovary", "CARCINOMA OF OVARY", "carcinoma of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Carcinoma", "shortest_name_length": 17}
{"curie": "UMLS:C1333556", "names": ["FIGO Stage IIIB GTT", "FIGO Stage IIIB Gestational Trophoblastic Tumor", "FIGO Stage IIIB Gestational Trophoblastic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Stage IIIB Gestational Trophoblastic Tumor", "shortest_name_length": 19}
{"curie": "MONDO:0011877", "names": ["OPTA1", "LRP5 osteopetrosis (disease)", "autosomal dominant osteopetrosis 1", "osteopetrosis, autosomal dominant 1", "OSTEOPETROSIS, AUTOSOMAL DOMINANT 1", "Osteopetrosis, Autosomal Dominant 1", "osteopetrosis autosomal dominant type 1", "Autosomal dominant osteopetrosis type 1", "Osteopetrosis autosomal dominant type 1", "autosomal dominant osteopetrosis type 1", "osteopetrosis, autosomal dominant type 1", "Osteopetrosis, Autosomal Dominant, Type I", "osteopetrosis, autosomal dominant, type 1", "OSTEOPETROSIS, AUTOSOMAL DOMINANT, TYPE I", "osteopetrosis (disease) caused by mutation in LRP5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant osteopetrosis 1", "shortest_name_length": 5}
{"curie": "UMLS:C5668153", "names": ["Lung Hyalinizing Clear Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Hyalinizing Clear Cell Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0001855", "names": ["Rubeotic iris", "rubeosis iridis", "Rubeosis iridis", "New vessels in iris", "NVI - New vessels iris", "Iris neovascularization", "Iris neovascularisation", "iris neovascularization", "neovascularization; iris", "iris; neovascularization", "Rubeosis iridis (disorder)", "rubeosis iridis (diagnosis)", "Neovascularization of the iris", "New blood vessel formation in iris"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rubeosis iridis", "shortest_name_length": 13}
{"curie": "MONDO:0019484", "names": ["hypothalamic hamartomas with gelastic seizures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypothalamic hamartomas with gelastic seizures", "shortest_name_length": 46}
{"curie": "UMLS:C1334924", "names": ["Sinonasal Disorder", "Nasal Cavity and Paranasal Sinus Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Disorder", "shortest_name_length": 18}
{"curie": "UMLS:C1336198", "names": ["Fallopian Tube Cancer Stage IIC", "Stage IIC Fallopian Tube Cancer", "AJCC Stage IIC Fallopian Tube Cancer", "FIGO Stage IIC Fallopian Tube Carcinoma", "Stage IIC Fallopian Tube Cancer AJCC v6", "Stage IIC Fallopian Tube Cancer AJCC v7", "FIGO Stage IIC Carcinoma of Fallopian Tube", "Stage IIC Fallopian Tube Cancer AJCC v6 and v7", "FIGO Stage IIC Carcinoma of the Fallopian Tube"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIC Fallopian Tube Cancer AJCC v6 and v7", "shortest_name_length": 31}
{"curie": "MONDO:0003740", "names": ["AIDS Phobia", "AIDS phobia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS phobia", "shortest_name_length": 11}
{"curie": "MONDO:0010399", "names": ["Complex GKD", "Del(X)(p21)", "monosomy Xp21", "Xp21- syndrome", "del(Xp21) syndrome", "partial monosomy Xp21", "deletion Xp21 syndrome", "Xp21 deletion syndrome", "chromosome Xp21 monosomy", "Xp21 microdeletion syndrome", "CHROMOSOME Xp21 DELETION SYNDROME", "chromosome Xp21 deletion syndrome", "COMPLEX GLYCEROL KINASE DEFICIENCY", "Complex Glycerol Kinase Deficiency", "complex glycerol kinase deficiency", "Complex glycerol kinase deficiency", "Complex Glycerol kinase deficiency", "Xp21 contiguous gene deletion syndrome", "Glycerol kinase deficiency-contiguous gene syndrome", "Glycerol kinase deficiency - contiguous gene syndrome", "Glycerol kinase deficiency - contiguous gene syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome Xp21 deletion syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0009660", "names": ["MPS4B", "MPS 4B", "MPSIVB", "MPS IVB", "MPS IV B", "Morquio-B Disease", "Morquio B Disease", "MORQUIO SYNDROME B", "Morquio Syndrome B", "Morquio B syndrome", "Morquio syndrome B", "Disease, Morquio-B", "Morquio B Syndrome", "Syndrome, Morquio B", "Morquio-like syndrome", "Morquio disease type B", "Morquio syndrome type B", "Morquio's Disease Type B", "Morquio Syndrome, Type B", "Mucopolysaccharidosis 4B", "Mucopolysaccharidosis 4Bs", "Mucopolysaccharidosis IV-B", "mucopolysaccharidosis type 4B", "Mucopolysaccharidosis type 4B", "mucopolysaccharidosis type IVB", "Mucopolysaccharidosis Type IVB", "Mucopolysaccharidosis type IVB", "mucopolysaccharidosis, type 4B", "Beta-D-galactosidase deficiency", "Mucopolysaccharidosis Type IVBs", "Mucopolysaccharidosis, MPS-IV-B", "beta-D-galactosidase deficiency", "mucopolysaccharidosis, type IVB", "Mucopolysaccharidosis Type IV B", "MUCOPOLYSACCHARIDOSIS, TYPE IVB", "Mucopolysaccharidosis, type IVB", "Morquio syndrome type B (diagnosis)", "MPS IV-B - Mucopolysaccharidosis IV-B", "mucopolysaccharidosis type IVB (Morquio)", "Mucopolysaccharidosis type IVB (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucopolysaccharidosis type 4B", "shortest_name_length": 5}
{"curie": "MONDO:0000050", "names": ["IGHD", "ICGHD", "GH Deficiency", "GH deficiency", "congenital IGHD", "pituitary dwarfism", "Somatotropin Deficiency", "Somatotropin deficiency", "Growth hormone deficiency", "growth hormone deficiency", "Growth Hormone Deficiency", "Isolated somatotropin deficiency", "congenital isolated GH deficiency", "Isolated growth hormone deficiency", "isolated growth hormone deficiency", "growth hormone deficiency (diagnosis)", "Isolated growth hormone insufficiency", "IGHD - Isolated growth hormone deficiency", "familial isolated growth hormone deficiency", "Isolated somatotropin deficiency (disorder)", "isolated congenital growth hormone deficiency", "congenital isolated growth hormone deficiency", "non-acquired isolated growth hormone deficiency", "Decreased response to growth hormone stimulation test"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated congenital growth hormone deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0008014", "names": ["nondisjunction", "NONDISJUNCTION", "mixoploidy, familial", "MIXOPLOIDY, FAMILIAL", "MOSAICISM, CHROMOSOMAL", "mosaicism, chromosomal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nondisjunction", "shortest_name_length": 14}
{"curie": "MONDO:0012993", "names": ["DUH2", "dyschromatosis universalis hereditaria 2", "DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 2", "Dyschromatosis Universalis Hereditaria 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyschromatosis universalis hereditaria 2", "shortest_name_length": 4}
{"curie": "MONDO:0005859", "names": ["uta", "Uta", "Breda", "Espundia", "ESPUNDIA", "espundia", "Chiclero ulcer", "CHICLERO ULCER", "sore; chiclero", "chiclero; sore", "L.braziliensis", "ulcer; chiclero", "chiclero; ulcer", "Chiclero's ulcer", "mucosal leishmaniasis", "Mucosal leishmaniasis", "chiclero ulcer or sore", "Neotropical leishmaniasis", "Leishmania mexicana complex", "mucocutaneous Leishmaniasis", "Mucocutaneous Leishmaniases", "Mucocutaneous Leishmaniasis", "Mucocutaneous leishmaniasis", "mucocutaneous leishmaniasis", "leishmaniasis; mucocutaneous", "Leishmaniasis, mucocutaneous", "Leishmaniases, Mucocutaneous", "Leishmaniasis, Mucocutaneous", "mucocutaneous; leishmaniasis", "Andean cutaneous leishmaniasis", "infection; Leishmania, mexicana", "Leishmania; infection, mexicana", "Leishmania braziliensis complex", "Infection by Leishmania mexicana", "American cutaneous leishmaniasis", "American Cutaneous Leishmaniasis", "Leishmania braziliensis infection", "Cutaneous leishmaniasis, American", "LEISHMANIASIS, AMERICAN CUTANEOUS", "cutaneous leishmaniasis, American", "Cutaneous, american leishmaniasis", "New World cutaneous leishmaniasis", "Leishmaniasis tegumentaria diffusa", "American; leishmaniasis, cutaneous", "leishmaniasis; American, cutaneous", "Leishmaniasis, cutaneous, American", "Leishmania; infection, braziliensis", "infection; Leishmania, braziliensis", "tegumentaria diffusa; leishmaniasis", "leishmaniasis; tegumentaria diffusa", "American mucocutaneous leishmaniasis", "Infection by Leishmania braziliensis", "Mucocutaneous leishmaniasis, American", "mucocutaneous leishmaniasis, American", "Leishmaniasis, mucocutaneous, American", "Infection caused by Leishmania mexicana", "Mucocutaneous leishmaniasis, (American)", "mucocutaneous leishmaniasis (diagnosis)", "Leishmania mexicana complex - infection", "mucocutaneous leishmaniasis, (American)", "Andean cutaneous leishmaniasis (diagnosis)", "Infection caused by Leishmania braziliensis", "American cutaneous leishmaniasis (diagnosis)", "Mucocutaneous infection caused by Leishmania", "American mucocutaneous leishmaniasis (disorder)", "Infection caused by Leishmania mexicana (disorder)", "Infection caused by Leishmania braziliensis (disorder)", "Mucocutaneous infection caused by Leishmania (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucocutaneous leishmaniasis", "shortest_name_length": 3}
{"curie": "UMLS:C2826320", "names": ["RN", "Refractory neutropenia", "neutropenia refractory", "Refractory Neutropenia", "Refractory neutropaenia", "Refractory neutropenia (disorder)", "Refractory neutropenia (diagnosis)", "Refractory neutropenia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Neutropenia", "shortest_name_length": 2}
{"curie": "MONDO:0015342", "names": ["Myelitis, Transverse", "acute myelitis transverse", "MYELITIS TRANSVERSE ACUTE", "acute transverse myelitis", "Acute Transverse Myelitis", "Acute transverse myelitis", "Myelitis, Acute Transverse", "Transverse Myelitis, Acute", "Acute (transverse) myelitis", "Acute transverse myelitis NOS", "Acute (transverse) myelitis NOS", "acute transverse myelitis of CNS", "Acute transverse myelitis (disorder)", "acute transverse myelitis of central nervous system", "acute transverse myelitis of central nervous system (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute transverse myelitis", "shortest_name_length": 20}
{"curie": "UMLS:C0015263", "names": ["Exercise Induced Bronchospasm", "Exercise-induced bronchospasm", "Exercise induced bronchospasm", "exercise induced bronchospasm", "Exercise-Induced Bronchospasm", "exercise-induced bronchospasm", "Bronchospasm, Exercise Induced", "Exercise-Induced Bronchospasms", "Bronchospasm, Exercise-Induced", "Exercise induced bronchospasm (disorder)", "exercise-induced bronchospasm (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bronchospasm, Exercise-Induced", "shortest_name_length": 29}
{"curie": "MONDO:0004629", "names": ["Subacute Delirium", "subacute delirium", "Subacute delirium", "Subacute Deliriums", "Delirium, Subacute", "Deliriums, Subacute", "Subacute confusional state", "Subacute delirium (disorder)", "delirium confusional state subacute", "Subacute confusional state (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subacute delirium", "shortest_name_length": 17}
{"curie": "MONDO:0023152", "names": ["Nucleus pulposus embolism", "fibrocartilaginous embolism", "Fibrocartilaginous embolism", "Embolism, fibrocartilaginous", "embolism, fibrocartilaginous"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibrocartilaginous embolism", "shortest_name_length": 25}
{"curie": "MONDO:0032933", "names": ["chromosome 1p36.33 duplication syndrome, atad3 gene cluster, autosomal dominant", "CHROMOSOME 1p36.33 DUPLICATION SYNDROME, ATAD3 GENE CLUSTER, AUTOSOMAL DOMINANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 1p36.33 duplication syndrome, atad3 gene cluster, autosomal dominant", "shortest_name_length": 79}
{"curie": "UMLS:C0080233", "names": ["loss teeth", "loss tooth", "TOOTH LOSS", "lost tooth", "Tooth Loss", "tooth loss", "Tooth lost", "teeth loss", "Tooth loss", "DENTAL LOSS", "loss dental", "Loss, Tooth", "Missing teeth", "Teeth missing", "loss of teeth", "missing teeth", "Loss of teeth", "tooth shedding", "Tooth loss, NOS", "Acquired edentia", "Shedding of tooth", "Loss of teeth, NOS", "Tooth loss (finding)", "tooth loss (symptom)", "Loss of teeth - acquired", "Loss of teeth (disorder)", "absence; teeth, acquired", "Missing tooth - acquired", "teeth; absence, acquired", "acquired absence of teeth", "Acquired absence of teeth", "Absence of tooth - acquired", "Acquired absence of teeth, NOS", "acquired absence of teeth (diagnosis)", "Acquired absence of teeth, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tooth Loss", "shortest_name_length": 10}
{"curie": "UMLS:C5235949", "names": ["Locally Advanced Alveolar Soft Part Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Alveolar Soft Part Sarcoma", "shortest_name_length": 43}
{"curie": "MONDO:0019095", "names": ["Pest", "pest", "Plague", "plague", "plagues", "Plague, NOS", "black death", "Yersiniosis", "Plague (disorder)", "Unspecified plague", "pestilential fever", "Pestilential fever", "plague (diagnosis)", "Plague, unspecified", "Yersinia pestis plague", "Yersinia pestis disease", "Yersinia pestis infection", "Yersinia pestis Infection", "infection; Yersinia pestis", "Yersinia pestis; infection", "Infection by Yersinia pestis", "infection by Yersinia pestis", "Pasteurella; infection, pestis", "infection; Pasteurella, pestis", "infection due to Yersinia pestis", "Yersinia pestis plague (diagnosis)", "Yersinia pestis infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "plague", "shortest_name_length": 4}
{"curie": "MONDO:0011637", "names": ["Sener syndrome", "SENER SYNDROME", "Frontonasal dysplasia and dilated virchow-robin spaces", "FRONTONASAL DYSPLASIA AND DILATED VIRCHOW-ROBIN SPACES", "frontonasal dysplasia and dilated Virchow-Robin spaces", "polycystic brain (cerebrum polycystica vera) associated with ectodermal dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sener syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0100294", "names": ["MC2D", "MC2DN1", "SDH Deficiency", "SDHx Deficiency", "Complex II deficiency", "Deficiency of Complex II", "Deficiency of fumarate reductase", "Respiratory Complex II Deficiency", "Respiratory complex II deficiency", "Deficiency of fumaric hydrogenase", "SUCCINATE DEHYDROGENASE DEFICIENCY", "Succinate CoQ Reductase Deficiency", "succinate CoQ reductase deficiency", "succinate dehydrogenase deficiency", "SUCCINATE CoQ REDUCTASE DEFICIENCY", "Succinate Dehydrogenase Deficiency", "mitochondrial complex 2 deficiency", "Succinate-CoQ Reductase Deficiency", "mitochondrial complex II deficiency", "Mitochondrial Complex II Deficiency", "Mitochondrial complex II deficiency", "Deficiency of succinic dehydrogenase", "Deficiency of succinate dehydrogenase", "Succinate-Coenzyme Q Reductase Deficiency", "Succinate-coenzyme Q reductase deficiency", "isolated succinate-CoQ reductase deficiency", "Decreased activity of mitochondrial complex II", "Deficiency of succinate dehydrogenase (disorder)", "isolated succinate-coenzyme Q reductase deficiency", "isolated succinate-ubiquinone reductase deficiency", "MITOCHONDRIAL COMPLEX II DEFICIENCY, NUCLEAR TYPE 1", "mitochondrial complex II deficiency, nuclear type 1", "complex 2 mitochondrial respiratory chain deficiency", "Succinate-coenzyme Q reductase deficiency (disorder)", "mitochondrial respiratory chain complex II deficiency", "isolated mitochondrial respiratory chain complex II deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex II deficiency, nuclear type 1", "shortest_name_length": 4}
{"curie": "MONDO:0012298", "names": ["GERSHONI-BARUCH SYNDROME", "Gershoni Baruch syndrome", "Gershoni-Baruch syndrome", "Gershoni-Baruch Syndrome", "Omphalocele, Diaphragmatic Hernia, And Radial Ray Defects", "omphalocele, diaphragmatic hernia, and radial ray defects", "OMPHALOCELE, DIAPHRAGMATIC HERNIA, AND RADIAL RAY DEFECTS", "Omphalocele-diaphragmatic hernia-cardiovascular anomalies-radial ray defect syndrome", "Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome", "Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "omphalocele, diaphragmatic hernia, and radial ray defects", "shortest_name_length": 24}
{"curie": "UMLS:C5420767", "names": ["Conjunctival Junctional Nevus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conjunctival Junctional Nevus", "shortest_name_length": 29}
{"curie": "MONDO:0002645", "names": ["Cerebritis", "CEREBRITIS", "cerebritis", "cerebral hemisphere inflammation", "inflammation of cerebral hemisphere"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebritis", "shortest_name_length": 10}
{"curie": "UMLS:C3697776", "names": ["PVL", "Papillary Leukoplakia", "Verrucous Oral Leukoplakia", "Proliferative verrucous leukoplakia", "Proliferative Verrucous Leukoplakia", "Proliferative verrucous oral leukoplakia", "Proliferative verrucous oral leukoplakia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Proliferative verrucous oral leukoplakia", "shortest_name_length": 3}
{"curie": "MONDO:0017073", "names": ["cervical spina bifida cystica"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical spina bifida cystica", "shortest_name_length": 29}
{"curie": "UMLS:C1333988", "names": ["Familial Male Breast Carcinoma", "Hereditary Male Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hereditary Male Breast Carcinoma", "shortest_name_length": 30}
{"curie": "UMLS:C0393691", "names": ["Occipital lobe epilepsy", "occipital lobe epilepsy", "Occipital Lobe Epilepsy", "Lobe Epilepsy, Occipital", "Occipital Lobe Epilepsies", "Epilepsies, Occipital Lobe", "Occipital lobe epilepsy (disorder)", "occipital lobe epilepsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Occipital Lobe Epilepsy", "shortest_name_length": 23}
{"curie": "MONDO:0800037", "names": ["MTTS1 MELAS syndrome", "MELAS syndrome caused by mutation in MTTS1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MELAS syndrome caused by mutation in MTTS1", "shortest_name_length": 20}
{"curie": "MONDO:0031115", "names": ["dyskinesia with orofacial involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyskinesia with orofacial involvement", "shortest_name_length": 37}
{"curie": "MONDO:0024573", "names": ["CMH", "Familial Ventricular Hypertrophy", "Ventricular Hypertrophy, Familial", "Hypertrophy, Familial Ventricular", "Hereditary Ventricular Hypertrophy", "Familial Ventricular Hypertrophies", "Ventricular Hypertrophy, Hereditary", "Hypertrophy, Hereditary Ventricular", "VENTRICULAR HYPERTROPHY, HEREDITARY", "Ventricular Hypertrophies, Familial", "Hereditary Ventricular Hypertrophies", "Hypertrophic Familial Cardiomyopathy", "hypertrophic familial cardiomyopathy", "Familial Hypertrophic Cardiomyopathy", "familial hypertrophic cardiomyopathy", "Cardiomyopathy, Familial Hypertrophic", "Ventricular Hypertrophies, Hereditary", "Hypertrophies, Hereditary Ventricular", "cardiomyopathy, familial hypertrophic", "CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC", "Hypertrophic Cardiomyopathy, Familial", "Familial Hypertrophic Cardiomyopathies", "Cardiomyopathy, Hypertrophic, Familial", "hereditary hypertrophic cardiomyopathy", "Cardiomyopathies, Familial Hypertrophic", "Asymmetric Septal Hypertrophy, Familial", "Hypertrophic Cardiomyopathies, Familial", "Primary familial hypertrophic cardiomyopathy", "Hypertrophic cardiomyopathy with genetic marker", "familial hypertrophic cardiomyopathy (diagnosis)", "Primary familial hypertrophic cardiomyopathy (disorder)", "Hypertrophic cardiomyopathy with genetic marker (disorder)", "familila or idiopathic hypertrophic obstructive cardiomyopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial hypertrophic cardiomyopathy", "shortest_name_length": 3}
{"curie": "MONDO:0020594", "names": ["vi nerve palsy", "ABDUCENS PALSY", "nerve vi palsy", "Abducens Palsy", "VI Nerve Palsy", "VI nerve palsy", "Abducens palsy", "Palsy, VI Nerve", "Palsy, Abducens", "6th Nerve Palsy", "6th nerve palsy", "Palsy, 6th Nerve", "VIth nerve palsy", "Abducens Palsies", "Sixth nerve palsy", "Palsies, VI Nerve", "Palsies, Abducens", "Sixth Nerve Palsy", "6th Nerve Palsies", "sixth nerve palsy", "Palsy, Sixth Nerve", "Palsies, 6th Nerve", "abducen nerve palsy", "Sixth Nerve Palsies", "VIth nerve disorder", "VIth Nerve Disorder", "Lateral Rectus Palsy", "Abducens Nerve Palsy", "Abducens nerve palsy", "Palsies, Sixth Nerve", "Lateral rectus palsy", "lateral rectus palsy", "VIth Nerve Paralysis", "abducens nerve palsy", "VIth nerve paralysis", "Sixth Nerve Paralysis", "Palsy, Lateral Rectus", "sixth nerve paralysis", "Sixth nerve paralysis", "Palsy, Abducens Nerve", "Abducens nerve disease", "abducens nerve paresis", "Cranial Nerve VI Palsy", "Lateral Rectus Palsies", "Abducens Nerve Disease", "Cranial nerve VI palsy", "abducens nerve disease", "Abducens Nerve Palsies", "Abducens nerve paresis", "abducens nerve disorder", "disorder abducens nerve", "Abducens nerve weakness", "Abducens nerve disorder", "Palsies, Abducens Nerve", "Abducens Nerve Diseases", "abducen nerve paralysis", "Abducens Nerve Disorder", "Palsies, Lateral Rectus", "Abducens Nerve Paralysis", "Abducens nerve paralysis", "Abducent nerve paralysis", "ABDUCENS NERVE PARALYSIS", "Sixth Cranial Nerve Palsy", "paralysis; abducent nerve", "Sixth cranial nerve palsy", "cranial nerve palsy sixth", "sixth cranial nerve palsy", "disease of abducens nerve", "Cranial Nerve VI Diseases", "[OBSOLETE] Abducens Palsy", "disorder of abducens nerve", "Disorder of abducens nerve", "Disorder of abducent nerve", "Abducens nerve disease, NOS", "VIth Cranial Nerve Diseases", "Disorder of cranial nerve 6", "Sixth cranial nerve disease", "Sixth cranial nerve disorder", "Sixth [abducent] nerve palsy", "Abducens (sixth) nerve palsy", "Sixth cranial nerve weakness", "Abducens nerve disorder, NOS", "Sixth Cranial Nerve Diseases", "Sixth or abducens nerve palsy", "Sixth cranial nerve paralysis", "Sixth Cranial Nerve Disorders", "sixth nerve palsy (diagnosis)", "LATERAL RECTUS MUSCLE PARALYSIS", "paralysis; cranial nerve, sixth", "Abducens nerve palsy (disorder)", "Sixth cranial nerve disease, NOS", "Sixth cranial nerve disorder, NOS", "abducens nerve disease or disorder", "Abducens nerve weakness (disorder)", "Abducens nerve disease or syndrome", "Abducens nerve disorder (disorder)", "disease or disorder of abducens nerve", "disease (or disorder); abducent nerve", "disorder of abducens nerve (diagnosis)", "Sixth cranial nerve disease or syndrome", "Lateral rectus muscle denervation paresis", "Lateral rectus muscle innervation disorder", "disease (or disorder); cranial nerve, sixth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "abducens nerve disorder", "shortest_name_length": 14}
{"curie": "UMLS:C5204620", "names": ["Bladder Hemangioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder Hemangioma", "shortest_name_length": 18}
{"curie": "UMLS:C4521821", "names": ["IIIA", "Stage IIIA Hilar Cholangiocarcinoma", "Stage IIIA Hilar Cholangiocarcinoma AJCC v8", "Stage IIIA Perihilar Cholangiocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Hilar Cholangiocarcinoma AJCC v8", "shortest_name_length": 4}
{"curie": "MONDO:0006896", "names": ["REFLUX ESOPHAGITIS", "Reflux esophagitis", "esophagitis peptic", "peptic esophagitis", "reflux esophagitis", "esophagitis reflux", "Reflux Esophagitis", "Peptic Esophagitis", "ESOPHAGITIS REFLUX", "Peptic esophagitis", "Peptic oesophagitis", "Esophagitis, Peptic", "Reflux oesophagitis", "ESOPHAGITIS, REFLUX", "peptic oesophagitis", "reflux oesophagitis", "esophagitis; reflux", "Esophagitis, Reflux", "reflux; esophagitis", "Peptic Esophagitides", "Reflux Esophagitides", "peptic reflux disease", "Esophagitides, Peptic", "Esophagitides, Reflux", "esophagitis refluxing", "Peptic reflux disease", "Peptic reflux esophagitis", "Peptic reflux oesophagitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peptic esophagitis", "shortest_name_length": 18}
{"curie": "UMLS:C4331346", "names": ["Stage IVC Hypopharyngeal Throat Cancer", "Stage IVC Hypopharyngeal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Hypopharyngeal Carcinoma AJCC v8", "shortest_name_length": 38}
{"curie": "MONDO:0015281", "names": ["Sinus Pause", "sinus pause", "SINUS PAUSE", "Sinus pause", "Sinus Arrest", "sinus; pause", "Arrest sinus", "ARREST SINUS", "Sinus arrest", "pauses sinus", "pause; sinus", "sinus arrest", "SINUS ARREST", "Silent atrium", "ARREST ATRIAL", "Arrest atrial", "sinus; arrest", "arrest; sinus", "Atrial arrest", "Atrial standstill", "Atrial Standstill", "atrial standstill", "SINUS ARREST/PAUSE", "Sinus arrest/pause", "Sinus Arrest/Pause", "Sinus pause or arrest", "Sinus arrest (disorder)", "Atrial arrest (disorder)", "Sinus Arrest by EKG Finding", "Sinus Arrest by ECG Finding", "Atrial standstill (disorder)", "atrial cardiomyopathy with heart block", "Atrial cardiomyopathy with heart block"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial standstill", "shortest_name_length": 11}
{"curie": "MONDO:0006126", "names": ["Cecum NET G1", "cecum NET G1", "caecum NET G1", "cecum carcinoid tumor", "Cecal carcinoid tumor", "cecal carcinoid tumor", "Cecum Carcinoid Tumor", "Cecal Carcinoid Tumor", "caecum carcinoid tumor", "caecal carcinoid tumor", "Caecum Carcinoid Tumor", "Caecal Carcinoid Tumor", "Caecal carcinoid tumour", "carcinoid tumor of cecum", "Carcinoid Tumor of Cecum", "Carcinoid tumor of the cecum", "Carcinoid Tumor of the Cecum", "carcinoid tumor of the cecum", "Cecum Neuroendocrine Tumor G1", "cecum neuroendocrine tumor G1", "Carcinoid tumour of the caecum", "caecum carcinoid tumor (disease)", "caecum neuroendocrine neoplasm G1", "grade 1 neuroendocrine neoplasm of caecum", "caecum neuroendocrine tumor, well differentiated, low grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cecum neuroendocrine tumor G1", "shortest_name_length": 12}
{"curie": "MONDO:0007693", "names": ["Hairy elbow", "hairy elbows", "Hairy elbows", "HAIRY ELBOWS", "Pilosity of elbow", "Hairy elbow syndrome", "Elbow hypertrichosis", "HYPERTRICHOSIS CUBITI", "hypertrichosis cubiti", "hairy elbows syndrome", "Hairy elbows syndrome", "Hypertrichosis cubiti", "Hypertrichosis cubiti (disorder)", "MacDermot-Patton-Williams syndrome", "MacDermot Patton Williams syndrome", "hypertrichosis cubiti-short stature syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrichosis cubiti-short stature syndrome", "shortest_name_length": 11}
{"curie": "UMLS:C0265103", "names": ["artery narrowed vertebral", "Vertebral Artery Stenosis", "vertebral artery stenosis", "artery stenosis vertebral", "Vertebral Artery Stenoses", "Vertebral artery stenosis", "Stenosis, Vertebral Artery", "Vertebral artery narrowing", "Artery Stenosis, Vertebral", "Stenoses, Vertebral Artery", "Artery Stenoses, Vertebral", "vertebral artery narrowing", "narrowing; vertebral artery", "stricture; vertebral artery", "Vertebral artery stenosis (disorder)", "vertebral artery stenosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vertebral Artery Stenosis", "shortest_name_length": 25}
{"curie": "MONDO:0012606", "names": ["MTBS2", "MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, 2", "mycobacterium tuberculosis, susceptibility to, 2", "Mycobacterium tuberculosis, susceptibility to, type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mycobacterium tuberculosis, susceptibility to, 2", "shortest_name_length": 5}
{"curie": "UMLS:C0743525", "names": ["Enterobacter sepsis", "ENTEROBACTER SEPSIS", "Enterobacter septicemia", "Enterobacter septicaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Enterobacter sepsis", "shortest_name_length": 19}
{"curie": "UMLS:C5448070", "names": ["Variant AIH", "Variant Autoimmune Hepatitis", "Autoimmune Hepatitis, Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Variant Autoimmune Hepatitis", "shortest_name_length": 11}
{"curie": "UMLS:C0863100", "names": ["tightness jaw", "jaw tightness", "tightness in jaw", "Tightness in jaw"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tightness in jaw", "shortest_name_length": 13}
{"curie": "MONDO:0008626", "names": ["Ureter, Bifid Or Double", "ureter, bifid or double", "URETER, BIFID OR DOUBLE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ureter, bifid or double", "shortest_name_length": 23}
{"curie": "UMLS:C4329645", "names": ["Cerebellar and Ventricular Ependymal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebellar and Ventricular Ependymal Tumor", "shortest_name_length": 42}
{"curie": "UMLS:C5207094", "names": ["Sinonasal Adenocarcinoma, Intestinal-Type with Papillary Pattern"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Adenocarcinoma, Intestinal-Type with Papillary Pattern", "shortest_name_length": 64}
{"curie": "MONDO:0025028", "names": ["vesicular stomatitis", "stomatitis vesicular", "Vesicular Stomatitis", "Vesicular stomatitis", "stomatitis, vesicular", "vesicular; stomatitis", "Stomatitis, Vesicular", "stomatitis; vesicular", "Vesicular Stomatitides", "vesicular Stomatitides", "Stomatitides, vesicular", "Stomatitides, Vesicular", "Vesicular stomatitis NOS", "Vesicular stomatitis, NOS", "Vesicular stomatitis (disorder)", "vesicular stomatitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vesicular stomatitis", "shortest_name_length": 20}
{"curie": "MONDO:0016438", "names": ["Elastotic striae", "linear focal elastosis", "linear focal dermal elastosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "linear focal dermal elastosis", "shortest_name_length": 16}
{"curie": "MONDO:0003952", "names": ["adult CNS choriocarcinoma", "Adult CNS Choriocarcinoma", "Choriocarcinoma of Adult CNS", "choriocarcinoma of adult CNS", "choriocarcinoma of the adult CNS", "Choriocarcinoma of the Adult CNS", "central nervous system choriocarcinoma", "Central Nervous System Choriocarcinoma", "Adult Central Nervous System Choriocarcinoma", "adult central nervous system choriocarcinoma", "Choriocarcinoma of Adult Central Nervous System", "choriocarcinoma of adult central nervous system", "Choriocarcinoma of the adult central nervous system", "choriocarcinoma of the adult central nervous system", "Choriocarcinoma of the Adult Central Nervous System", "adult choriocarcinoma of the central nervous system", "choriocarcinoma of the central nervous system of adults"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult central nervous system choriocarcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0005375", "names": ["nasopharynx tumor", "Nasopharynx--Tumors", "Tumor of Nasopharynx", "NASOPHARYNGEAL TUMOR", "Tumor of nasopharynx", "nasopharynx neoplasm", "nasopharyngeal tumor", "Nasopharynx Neoplasm", "Nasopharyngeal tumor", "tumor of nasopharynx", "Nasopharyngeal Tumor", "Neoplasm, Nasopharynx", "nasopharyngeal tumors", "Nasopharynx Neoplasms", "Tumour of nasopharynx", "Nasopharyngeal tumour", "Neoplasms, Nasopharynx", "Neoplasm of nasopharynx", "Nasopharyngeal neoplasm", "neoplasm of nasopharynx", "nasopharyngeal neoplasm", "Nasopharyngeal Neoplasm", "Neoplasm of Nasopharynx", "Nasopharyngeal Neoplasms", "Tumor of postnasal space", "nasopharyngeal neoplasms", "tumor of the nasopharynx", "Neoplasm, Nasopharyngeal", "Tumor of the Nasopharynx", "Tumor of the nasopharynx", "Tumour of postnasal space", "Tumour of the nasopharynx", "Neoplasms, Nasopharyngeal", "Neoplasm of the nasopharynx", "Neoplasm of the Nasopharynx", "neoplasm of the nasopharynx", "Neoplasia of the nasopharynx", "nasopharynx neoplasm (disease)", "Neoplasm of nasopharynx (disorder)", "neoplasm of nasopharynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasopharyngeal neoplasm", "shortest_name_length": 17}
{"curie": "MONDO:0002162", "names": ["Fallopian Tube Adenosarcoma", "fallopian tube adenosarcoma", "adenosarcoma of fallopian tube", "fallopian tube Müllerian adenosarcoma", "Fallopian Tube Mullerian Adenosarcoma", "fallopian tube mullerian adenosarcoma", "fallopian tube Mullerian adenosarcoma", "Fallopian Tube Müllerian Adenosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fallopian tube adenosarcoma", "shortest_name_length": 27}
{"curie": "UMLS:C0586557", "names": ["Work accident", "accidents work", "accidents works", "Accident at work", "accident at work", "Accident at work, NOS", "Accident while engaged in work-related activity", "Accident whilst engaged in work-related activity", "ACCIDENTS WHILE ENGAGED IN WORK-RELATED ACTIVITIES", "Accident while engaged in work-related activity, NOS", "Accident while engaged in work-related activity (event)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Accident while engaged in work-related activity", "shortest_name_length": 13}
{"curie": "MONDO:0044207", "names": ["SGD1", "specific granule deficiency", "SPECIFIC GRANULE DEFICIENCY 1", "specific granule deficiency 1", "CEBPE specific granule deficiency", "lactoferrin-deficient neutrophils", "neutrophil lactoferrin deficiency", "specific granule deficiency caused by mutation in CEBPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "specific granule deficiency 1", "shortest_name_length": 4}
{"curie": "UMLS:C0347536", "names": ["Superficial Head Injury", "SUPERFICIAL HEAD TRAUMA", "HEAD INJURY SUPERFICIAL", "superficial injury head", "Head Injury, Superficial", "Injury, Superficial Head", "Superficial Head Injuries", "Superficial injury of head", "Head Injuries, Superficial", "Injuries, Superficial Head", "Superficial injury of head (disorder)", "Superficial injury of head (diagnosis)", "Superficial injury of head, part unspecified", "Superficial injury of unspecified part of head", "Superficial injury of head, part unspecified, unspecified", "Unspecified superficial injury of unspecified part of head"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Head Injury, Superficial", "shortest_name_length": 23}
{"curie": "UMLS:C1697454", "names": ["Pelvic fluid collection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pelvic fluid collection", "shortest_name_length": 23}
{"curie": "MONDO:0004554", "names": ["pediatric renal Angiomyolipoma", "pediatric renal angiomyolipoma", "Pediatric Renal Angiomyolipoma", "childhood renal angiomyolipoma", "Childhood Renal Angiomyolipoma", "Childhood Kidney Angiomyolipoma", "childhood kidney angiomyolipoma", "pediatric kidney angiomyolipoma", "Pediatric Kidney Angiomyolipoma", "kidney angiomyolipoma of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood kidney angiomyolipoma", "shortest_name_length": 30}
{"curie": "MONDO:0009135", "names": ["CDA Ia", "CDAN1A", "CDA, TYPE Ia", "congenital dyserythropoietic anemia type Ia", "anemia, congenital dyserythropoietic, type 1", "ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ia", "dyserythropoietic Anemia, congenital, type Ia", "DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE Ia", "anemia, congenital dyserythropoietic, type 1a", "anemia, congenital dyserythropoietic, type Ia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anemia, congenital dyserythropoietic, type 1a", "shortest_name_length": 6}
{"curie": "MONDO:0011100", "names": ["microcephaly, retinitis pigmentosa, and sutural cataract", "Microcephaly, Retinitis Pigmentosa, and Sutural Cataract", "MICROCEPHALY, RETINITIS PIGMENTOSA, AND SUTURAL CATARACT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly, retinitis pigmentosa, and sutural cataract", "shortest_name_length": 56}
{"curie": "MONDO:0011070", "names": ["VMLDS1", "Van Maldergem syndrome", "van Maldergem syndrome 1", "Van Maldergem syndrome 1", "VAN MALDERGEM SYNDROME 1", "VAN Maldergem syndrome 1", "Van Maldergem Syndrome 1", "DCHS1 van Maldergem syndrome", "Van Maldergem syndrome type 1", "CEREBROFACIOARTICULAR SYNDROME", "cerebrofacioarticular syndrome", "Cerebrofacioarticular syndrome", "Cerebro-facio-articular syndrome", "Van Maldergem Wetzburger Verloes syndrome", "Cerebrofacioarticular syndrome (disorder)", "cerebrofacioarticular syndrome (diagnosis)", "Cerebro-facio-articular syndrome of Van Maldergem", "van Maldergem syndrome caused by mutation in DCHS1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "van Maldergem syndrome 1", "shortest_name_length": 6}
{"curie": "MONDO:0007398", "names": ["CRANIORHINY", "craniorhiny", "Craniorhiny", "Craniorhiny (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniorhiny", "shortest_name_length": 11}
{"curie": "UMLS:C0012254", "names": ["digitalis toxicity", "Digitalis toxicity", "Digitalis Toxicity", "DIGITALIS TOXICITY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Digitalis toxicity", "shortest_name_length": 18}
{"curie": "MONDO:0012957", "names": ["MS3", "multiple sclerosis, susceptibility to, 3", "MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple sclerosis, susceptibility to, 3", "shortest_name_length": 3}
{"curie": "MONDO:0002386", "names": ["MEST", "Benign MEST", "benign MEST", "adult mesoblastic nephroma", "Renal Epithelial Stromal Tumor", "Kidney Mixed Epithelial and Stromal Tumor", "Mixed epithelial and stromal tumor of kidney", "Mixed Epithelial Stromal Tumor of the Kidney", "mixed epithelial stromal tumor of the kidney", "mixed epithelial and stromal tumour of kidney", "Mixed epithelial and stromal tumour of kidney", "Benign Kidney Mixed Epithelial and Stromal Tumor", "Benign mixed epithelial and stromal tumor of kidney", "Benign Mixed Epithelial Stromal Tumor of the Kidney", "Benign mixed epithelial and stromal tumour of kidney", "Benign mixed epithelial and stromal tumor of kidney (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed epithelial stromal tumor of the kidney", "shortest_name_length": 4}
{"curie": "UMLS:C5557150", "names": ["Stage IA Cervical Cancer AJCC v9", "Stage IA Cervical Carcinoma AJCC v9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Cervical Cancer AJCC v9", "shortest_name_length": 32}
{"curie": "MONDO:0007411", "names": ["ADCL1", "cutis laxa, autosomal dominant", "autosomal dominant cutis laxa-1", "autosomal dominant cutis laxa 1", "CUTIS LAXA, AUTOSOMAL DOMINANT 1", "cutis laxa, autosomal dominant 1", "ELN autosomal dominant cutis laxa", "cutis laxa autosomal dominant adcl1", "cutis laxa, autosomal dominant type 1", "autosomal dominant cutis laxa-1 (diagnosis)", "autosomal dominant cutis laxa caused by mutation in ELN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutis laxa, autosomal dominant 1", "shortest_name_length": 5}
{"curie": "UMLS:C2986867", "names": ["Thymus Solitary Fibrous Tumor", "Thymic Solitary Fibrous Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thymus Solitary Fibrous Tumor", "shortest_name_length": 29}
{"curie": "UMLS:C3160770", "names": ["Minor bleed"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Minor bleed", "shortest_name_length": 11}
{"curie": "UMLS:C2103465", "names": ["posterior fossa tumor", "fossa posterior tumor", "fossa posterior tumors", "posterior fossa tumors", "Posterior Fossa Neoplasm", "Posterior Cranial Fossa Tumor", "Posterior Cranial Fossa Neoplasm", "neoplasm of posterior cranial fossa", "neoplasm of posterior cranial fossa (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Posterior Fossa Neoplasm", "shortest_name_length": 21}
{"curie": "MONDO:0020175", "names": ["skin of eyelid cancer", "Malignant Eyelid Tumor", "eyelid malignant tumor", "eyelid malignant tumors", "cancer of skin of eyelid", "malignant tumor of eyelid", "Malignant tumor of eyelid", "Malignant Tumor of Eyelid", "Malignant Eyelid Neoplasm", "Malignant tumour of eyelid", "malignant neoplasm of eyelid", "Malignant Neoplasm of Eyelid", "Malignant neoplasm of eyelid", "Malignant Tumor of the Eyelid", "skin neoplasm eyelid malignant", "Malignant Neoplasm of the Eyelid", "malignant skin of eyelid neoplasm", "malignant neoplasm of skin of eyelid", "Malignant neoplasm of skin of eyelid", "malignant tumor of palpebral epidermis", "Malignant neoplasm of eyelid (disorder)", "malignant neoplasm of eyelid (diagnosis)", "neoplasm of ocular adnexa eyelid malignant", "Malignant neoplasm of skin of eyelid (disorder)", "malignant neoplasm of skin of eyelid (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant tumor of palpebral epidermis", "shortest_name_length": 21}
{"curie": "UMLS:C2987406", "names": ["Gastric Intramucosal Carcinoma", "Gastric Intramucosal Adenocarcinoma", "Gastric Intramucosal Invasive Neoplasia", "Gastric Intramucosal Invasive Neoplasia/ Intramucosal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Intramucosal Adenocarcinoma", "shortest_name_length": 30}
{"curie": "UMLS:C5419164", "names": ["COVID-19-Associated Acute Respiratory Distress Syndrome", "SARS-CoV-2-Associated Acute Respiratory Distress Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "COVID-19-Associated Acute Respiratory Distress Syndrome", "shortest_name_length": 55}
{"curie": "MONDO:0002674", "names": ["Stricture or kinking of ureter", "stricture or kinking of ureter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stricture or kinking of ureter", "shortest_name_length": 30}
{"curie": "MONDO:0014857", "names": ["NEDBEH", "rere-related neurodevelopmental syndrome", "neurodevelopmental disorder with or without anomalies of the brain, eye, or heart", "NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART", "neurodevelopmental disorder with or without anomalies of the brain, eye, or heart; NEDBEH"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with or without anomalies of the brain, eye, or heart", "shortest_name_length": 6}
{"curie": "UMLS:C5206653", "names": ["Localized Head and Neck Carcinoma", "Non-Metastatic Head and Neck Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized Head and Neck Carcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C4087290", "names": ["Obsessive-compulsive symptom"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Obsessive-compulsive symptom", "shortest_name_length": 28}
{"curie": "MONDO:0022098", "names": ["Catamenial pneumothorax", "catamenial pneumothorax", "pneumothorax catamenial", "premenstrual pneumothorax", "Premenstrual pneumothorax", "Catamenial pneumothorax (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "catamenial pneumothorax", "shortest_name_length": 23}
{"curie": "MONDO:0017714", "names": ["Acyl-CoA dehydrogenase deficiency", "acyl-CoA dehydrogenase deficiency", "Deficiency of acyl-CoA dehydrogenase", "Acyl-CoA dehydrogenase deficiency, NOS", "Acyl-coenzyme A dehydrogenase deficiency", "acyl-CoA dehydrogenase deficiency (diagnosis)", "Acyl-coenzyme A dehydrogenase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acyl-CoA dehydrogenase deficiency", "shortest_name_length": 33}
{"curie": "UMLS:C5555067", "names": ["Secondary Central Atypical Cartilaginous Tumor/Chondrosarcoma, Grade 1", "Secondary Conventional Central Atypical Cartilaginous Tumor/Chondrosarcoma, Grade 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary Central Atypical Cartilaginous Tumor/Chondrosarcoma, Grade 1", "shortest_name_length": 70}
{"curie": "MONDO:0001185", "names": ["Amnesia neurosis", "psychogenic amnesia", "Psychogenic amnesia", "dissociative amnesia", "amnesia dissociative", "Dissociative amnesia", "Dissociative Amnesia", "dissociative; amnesia", "Amnesia, Dissociative", "amnesia; dissociative", "Dissociative Amnesias", "Amnesias, Dissociative", "Psychogenic amnesia (disorder)", "dissociative amnesia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dissociative amnesia", "shortest_name_length": 16}
{"curie": "MONDO:0007751", "names": ["FHCL2", "FCHL2", "IIb en III; Frederickson", "Frederickson; IIb en III", "Familial defective apoB100", "Hyperapobetalipoproteinemia", "Hyperapobetalipoproteinaemia", "HYPERLIPOPROTEINEMIA TYPE IIB", "Type IIb hyperlipoproteinemia", "Hyperlipoproteinemia Type IIb", "Hyperlipoproteinemia Type IIbs", "Type IIb hyperlipoproteinaemia", "Familial Hypercholesterolemia 2", "hypercholesterolemia, familial, 2", "Hypercholesterolemia, Familial, 2", "HYPERCHOLESTEROLEMIA, FAMILIAL, 2", "Familial hyperlipoproteinemia type IIb", "Familial Combined Hyperlipoproteinemia", "Autosomal Dominant Hypercholesterolemia", "Combined Hyperlipoproteinemia, Familial", "Familial hyperlipoproteinaemia type IIb", "Familial defective apolipoprotein B-100", "FCHL - Familial combined hyperlipidemia", "Familial Combined Hyperlipoproteinemias", "familial defective apolipoprotein B-100", "Hyperlipoproteinemia, Familial Combined", "APOLIPOPROTEIN B-100, FAMILIAL DEFECTIVE", "Apolipoprotein B-100, Familial Defective", "FCHL - Familial combined hyperlipidaemia", "Apolipoprotein B 100, Familial Defective", "apolipoprotein B-100, familial defective", "Combined Hyperlipoproteinemias, Familial", "Hyperlipoproteinemias, Familial Combined", "Fredrickson type IIb hyperlipoproteinemia", "Fredrickson Type IIb hyperlipoproteinemia", "Fredrickson type IIb hyperlipoproteinaemia", "Fredrickson; type IIb hyperlipoproteinemia", "Fredrickson Type IIb hyperlipoproteinaemia", "hyperlipoproteinemia; Fredrickson type IIb", "Hyperlipoproteinemia, Frederickson type IIb", "FDB - Familial defective apolipoprotein B-100", "APOLIPOPROTEIN B-100, FAMILIAL LIGAND-DEFECTIVE", "apolipoprotein B-100, familial ligand-defective", "Apolipoprotein B 100, Familial Ligand Defective", "Apolipoprotein B-100, Familial Ligand-Defective", "HYPERCHOLESTEROLEMIA, AUTOSOMAL DOMINANT, TYPE B", "Hypercholesterolemia, Autosomal Dominant, Type B", "prebetalipoproteinemia; hyperbetalipoproteinemia", "Fredrickson Type IIb or III hyperlipoproteinemia", "hypercholesterolemia, autosomal dominant, type B", "Familial defective apolipoprotein B-100 (disorder)", "familial defective apolipoprotein B-100 (diagnosis)", "Fredrickson's hyperlipoproteinemia, type IIb or III", "Hyperbetalipoproteinemia with prebetalipoproteinemia", "hyperbetalipoproteinemia; with prebetalipoproteinemia", "HYPERCHOLESTEROLEMIA, FAMILIAL, DUE TO LIGAND-DEFECTIVE APOLIPOPROTEIN B", "Hypercholesterolemia, familial, due to ligand-defective apolipoprotein B", "hypercholesterolemia, familial, due to ligand-defective apolipoprotein B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypercholesterolemia, autosomal dominant, type B", "shortest_name_length": 5}
{"curie": "MONDO:0021499", "names": ["Benign Cerebellar Tumor", "benign cerebellar tumor", "cerebellum benign neoplasm", "benign tumor of cerebellum", "Benign Tumor of Cerebellum", "benign cerebellar neoplasm", "Benign Cerebellar Neoplasm", "Benign Cerebellar Neoplasms", "Cerebellar Neoplasm, Benign", "benign cerebellar neoplasms", "Neoplasm, Benign Cerebellar", "Cerebellar Neoplasms, Benign", "cerebellar neoplasms, benign", "neoplasms, cerebellar, benign", "benign neoplasm of cerebellum", "Neoplasms, Cerebellar, Benign", "Neoplasms, Benign, Cerebellar", "neoplasms, benign, cerebellar", "Benign Neoplasm of Cerebellum", "Benign neoplasm of cerebellum", "Benign Tumor of the Cerebellum", "benign tumor of the cerebellum", "Benign Neoplasm of the Cerebellum", "benign neoplasm of the cerebellum", "Benign neoplasm of cerebellum, NOS", "Benign neoplasm of cerebellum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of cerebellum", "shortest_name_length": 23}
{"curie": "UMLS:C1333141", "names": ["Conditioned Insomnia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conditioned Insomnia", "shortest_name_length": 20}
{"curie": "MONDO:0007305", "names": ["cervical vertebral dysplasia", "Cervical vertebral dysplasia", "Cervical Vertebral Dysplasia", "CERVICAL VERTEBRAL DYSPLASIA", "cervical vertebral dysplasia (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical vertebral dysplasia", "shortest_name_length": 28}
{"curie": "MONDO:0700193", "names": ["Chicken Monocytic Leukemia", "chicken monocytic leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chicken monocytic leukemia", "shortest_name_length": 26}
{"curie": "UMLS:C5446379", "names": ["Non-Neoplastic Lacrimal System Disorder", "Non-Neoplastic Lacrimal Apparatus Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Lacrimal System Disorder", "shortest_name_length": 39}
{"curie": "UMLS:C0270942", "names": ["Myasthenic crisis", "Myasthenia gravis crisis", "Myasthenia gravis in crisis", "Myasthenic crisis (disorder)", "myasthenia gravis with acute exacerbation", "Myasthenia gravis with (acute) exacerbation", "myasthenia gravis with acute exacerbation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myasthenic crisis", "shortest_name_length": 17}
{"curie": "UMLS:C2931319", "names": ["Systemic necrotizing angitis", "Systemic necrotizing angiitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Systemic necrotizing angiitis", "shortest_name_length": 28}
{"curie": "MONDO:0030318", "names": ["SCAR30", "autosomal recessive spinocerebellar ataxia 30", "spinocerebellar ataxia, autosomal recessive 30", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 30"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia, autosomal recessive 30", "shortest_name_length": 6}
{"curie": "MONDO:0018788", "names": ["COL4A1 or COL4A2-related cerebral angiopathy", "COL4A1 or COL4A2-related cerebral small vessel disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "COL4A1 or COL4A2-related cerebral small vessel disease", "shortest_name_length": 44}
{"curie": "MONDO:0006362", "names": ["peritoneal mesothelioma", "mesothelioma peritoneum", "Peritoneal mesothelioma", "peritoneum mesothelioma", "Peritoneal Mesothelioma", "mesothelioma; peritoneum", "peritoneum; mesothelioma", "Mesothelioma of Peritoneum", "mesothelioma of peritoneum", "Mesothelioma of peritoneum", "mesothelioma of the peritoneum", "Mesothelioma of the Peritoneum", "Malignant Peritoneal Mesothelioma", "Peritoneal Malignant Mesothelioma", "Peritoneal mesothelioma malignant", "Malignant peritoneal mesothelioma", "peritoneal mesothelioma (disease)", "malignant mesothelioma of peritoneum", "Malignant Mesothelioma of Peritoneum", "Malignant mesothelioma of peritoneum", "Cancer of the peritoneum, mesothelioma", "Malignant Mesothelioma of the Peritoneum", "Primary malignant peritoneal mesothelioma", "Diffuse malignant peritoneal mesothelioma", "Malignant mesothelioma of peritoneum (disorder)", "malignant mesothelioma of peritoneum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peritoneal mesothelioma", "shortest_name_length": 23}
{"curie": "MONDO:0020158", "names": ["eyelids malposition disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eyelids malposition disorder", "shortest_name_length": 28}
{"curie": "MONDO:0009627", "names": ["GAMOS", "CAMOS", "Galloway syndrome", "GALLOWAY SYNDROME", "galloway syndrome", "Galloway-Mowat Syndrome", "galloway mowat syndrome", "Galloway Mowat syndrome", "Galloway-Mowat syndrome", "galloway-mowat syndrome", "Nephrosis-Microcephaly Syndrome", "Microcephaly nephrosis syndrome", "NEPHROSIS-MICROCEPHALY SYNDROME", "nephrosis-microcephaly syndrome", "microcephaly nephrosis syndrome", "Galloway Mowat syndrome (disorder)", "Galloway Mowat syndrome (diagnosis)", "nephrosis-neural dysmigration syndrome", "nephrosis neuronal dysmigration syndrome", "Nephrosis-Neuronal Dysmigration Syndrome", "Nephrosis-neuronal dysmigration syndrome", "NEPHROSIS-NEURONAL DYSMIGRATION SYNDROME", "Nephrosis neuronal dysmigration syndrome", "nephrosis-neuronal dysmigration syndrome", "Nephrosis, neuronal dysmigration syndrome", "spinocerebellar ataxia, autosomal recessive 5", "Microcephaly-hiatus hernia-nephrotic syndrome", "nephrosis-microcephaly-hiatus hernia syndrome", "microcephaly-hiatus hernia-nephrotic syndrome", "hiatus hernia-microcephaly-nephrosis syndrome", "Microcephaly, hiatus hernia, nephrotic syndrome", "congenital malformation syndromes Galloway Mowat", "Microcephaly, hiatal hernia and nephrotic syndrome", "microcephaly, hiatal hernia and nephrotic syndrome", "Microcephaly, Hiatus Hernia, And Nephrotic Syndrome", "microcephaly, hiatal hernia, and nephrotic syndrome", "hiatal hernia-microcephaly-nephrosis, Galloway type", "MICROCEPHALY, HIATAL HERNIA, AND NEPHROTIC SYNDROME", "spinocerebellar ataxia, autosomal recessive 5, formerly", "congenital microcephaly-hiatus hernia-nephrotic syndrome", "microcephaly-infantile spasms-psychomotor retardation-nephrotic syndrome", "cerebellar ataxia with mental retardation, optic atrophy, and skin abnormalities", "CEREBELLAR ATAXIA WITH MENTAL RETARDATION, OPTIC ATROPHY, AND SKIN ABNORMALITIES", "cerebellar ataxia with intellectual disability, optic atrophy, and skin abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Galloway-Mowat syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C2985218", "names": ["Substance-Induced Anxiety Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Substance-Induced Anxiety Disorder", "shortest_name_length": 34}
{"curie": "MONDO:0004713", "names": ["lower gum cancer", "gingiva of lower jaw cancer", "Malignant tumor of lower gum", "malignant tumor of lower gum", "malignant lower gum neoplasm", "malignant tumour of lower gum", "Malignant tumour of lower gum", "cancer of gingiva of lower jaw", "malignant neoplasm of lower gum", "Malignant neoplasm of lower gum", "malignant tumor of lower gingiva", "Malignant tumor of lower gingiva", "Malignant tumour of lower gingiva", "malignant gingiva of lower jaw neoplasm", "malignant neoplasm of gingiva of lower jaw", "Malignant tumor of lower gingiva (disorder)", "malignant neoplasm of lower gum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lower gum cancer", "shortest_name_length": 16}
{"curie": "MONDO:0015033", "names": ["HCHWAD", "HCHWA-D", "HCHWA, Dutch type", "ABetaE22Q amyloidosis", "Dutch type amyloidosis", "ABeta amyloidosis, Dutch type", "ABeta amyloidosis, dutch type", "Dutch Type Hereditary Cerebral Amyloid Angiopathy", "Hereditary cerebral amyloid angiopathy, Dutch type", "Hereditary Cerebral Amyloid Angiopathy, Dutch Type", "CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, DUTCH VARIANT", "cerebral amyloid angiopathy, APP-related, Dutch variant", "Cerebral Amyloid Angiopathy, App-Related, Dutch Variant", "hereditary cerebral hemorrhage with amyloidosis, Dutch type", "Hereditary cerebral hemorrhage with amyloidosis, Dutch type", "Cerebral hemorrhage with amyloidosis, hereditary, Dutch type", "Hereditary cerebral hemorrhage with amyloidosis - Dutch type", "Hereditary cerebral amyloid angiopathy, Dutch type (disorder)", "Hereditary cerebral haemorrhage with amyloidosis - Dutch type", "AMYLOIDOSIS, HEREDITARY, WITH CEREBRAL HEMORRHAGE, DUTCH VARIANT", "Amyloidosis, Hereditary, With Cerebral Hemorrhage, Dutch Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ABeta amyloidosis, dutch type", "shortest_name_length": 6}
{"curie": "MONDO:0600016", "names": ["AcDys", "acinar dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acinar dysplasia", "shortest_name_length": 5}
{"curie": "UMLS:C0262497", "names": ["GLOBAL AMNESIA", "global amnesia", "Global amnesia", "Global Amnesia", "amnesia global", "Global Amnesias", "Amnesia, Global", "Amnesias, Global"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Global Amnesia", "shortest_name_length": 14}
{"curie": "UMLS:C5446662", "names": ["Unresectable Malignant Glomus Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Malignant Glomus Tumor", "shortest_name_length": 35}
{"curie": "MONDO:0013552", "names": ["SPG52", "CPSQ6", "CPSQ6, FORMERLY", "hereditary spastic paraplegia 52", "AP4S1 hereditary spastic paraplegia", "hereditary spastic paraplegia type 52", "spastic quadriplegic cerebral palsy 6", "cerebral palsy, spastic quadriplegic, 6", "autosomal recessive spastic paraplegia 52", "SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE", "spastic paraplegia 52, autosomal recessive", "cerebral palsy, spastic quadriplegic, 6, formerly", "CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 6, FORMERLY", "hereditary spastic paraplegia caused by mutation in AP4S1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 52", "shortest_name_length": 5}
{"curie": "MONDO:0002650", "names": ["Scrotal Cancer", "scrotal cancer", "scrotum carcinoma", "Scrotal Carcinoma", "cancer of scrotum", "scrotal carcinoma", "Cancer of Scrotum", "carcinoma of scrotum", "Carcinoma of Scrotum", "Cancer of the Scrotum", "cancer of the scrotum", "carcinoma of the scrotum", "Carcinoma of the Scrotum", "carcinoma of scrotum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scrotal carcinoma", "shortest_name_length": 14}
{"curie": "UMLS:C1336298", "names": ["Peripheral T-Cell Lymphoma Stage II", "Stage II Peripheral T-cell Lymphoma", "Stage II Mature T- and NK-Cell Lymphoma", "Ann Arbor Stage II Mature T- and NK-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage II Mature T- and NK-Cell Lymphoma", "shortest_name_length": 35}
{"curie": "MONDO:0018809", "names": ["idiopathic peliosis hepatis", "idiopathic peliosis hepatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic peliosis hepatis", "shortest_name_length": 27}
{"curie": "MONDO:0000705", "names": ["C. diff Colitis", "C. diff colitis", "C. diff infection", "Janbon's syndrome", "C.difficile colitis", "c.difficile colitis", "c difficile colitis", "Pseudomembranous Colitis", "colitis pseudomembranous", "Colitis pseudomembranous", "Pseudomembranous colitis", "PSEUDOMEMBRANOUS COLITIS", "Antibiotic enterocolitis", "pseudomembranous colitis", "COLITIS PSEUDOMEMBRANOUS", "Clostridium enterocolitis", "Pseudomembraneous colitis", "antibiotics enterocolitis", "Colitis, Pseudomembranous", "Clostridium Enterocolitis", "antibiotic-induced colitis", "ENTERITIS PSEUDOMEMBRANOUS", "Antibiotic-induced colitis", "Enteritis pseudomembranous", "Pseudomembranous Enteritis", "Enteritis, Pseudomembranous", "clostridia difficile colitis", "COLITIS CLOSTRIDIA DIFFICILE", "Clostridioides enterocolitis", "Clostridium Difficile Colitis", "Antibiotic Associated Colitis", "antibiotic-associated colitis", "clostridium difficile colitis", "Antibiotic-Associated Colitis", "Clostridium difficile colitis", "CLOSTRIDIUM DIFFICILE COLITIS", "antibiotic associated colitis", "Antibiotic-associated colitis", "Antibiotic associated colitis", "Clostridium difficile Colitis", "Colitis;psuedomemb;C.difficile", "enterocolitis pseudomembranous", "Colitis, Antibiotic-Associated", "Pseudomembranous enterocolitis", "PSEUDOMEMBRANOUS ENTEROCOLITIS", "ENTEROCOLITIS PSEUDOMEMBRANOUS", "antibiotics associated colitis", "Pseudomembramous enterocolitis", "Enterocolitis pseudomembranous", "PMC - Pseudomembranous colitis", "pseudomembranous enterocolitis", "Pseudomembranous Enterocolitis", "Clostridium difficile infection", "Enterocolitis, Pseudomembranous", "Antibiotic enterocolitis syndrome", "clostridium difficile enterocolitis", "Antibiotic enterocolitis (disorder)", "pseudomembranous colitis (diagnosis)", "enterocolitis; Clostridium difficile", "Clostridium; difficile, enterocolitis", "ENTEROCOLITIS, PSEUDOMEMBRANOUS, ACUTE", "Clostridium difficile colitis (disorder)", "Clostridium difficile colitis (diagnosis)", "antibiotic associated colitis (diagnosis)", "Clostridioides difficile colitis (disease)", "Clostridioides difficile caused colitis (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clostridium difficile colitis", "shortest_name_length": 15}
{"curie": "MONDO:0021210", "names": ["trachea tumor", "Trachea Tumor", "Tracheal Tumor", "tracheal tumor", "trachea neoplasm", "Trachea Neoplasm", "Tumor of trachea", "Tumor of Trachea", "tumor of trachea", "Tumour of trachea", "Tracheal neoplasm", "Tracheal Neoplasm", "tracheal neoplasm", "Neoplasm, Tracheal", "Tracheal Neoplasms", "neoplasm of trachea", "Neoplasm of Trachea", "Neoplasms, Tracheal", "Neoplasm of trachea", "Tumor of the Trachea", "tumor of the trachea", "Tracheal neoplasm NOS", "Neoplasm of the trachea", "neoplasm of the trachea", "Neoplasm of the Trachea", "trachea neoplasm (disease)", "Neoplasm of trachea (disorder)", "neoplasm of trachea (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trachea neoplasm", "shortest_name_length": 13}
{"curie": "UMLS:C0340278", "names": ["atrial hypertrophy", "Atrial hypertrophy", "Atrial hypertrophy (disorder)", "atrial hypertrophy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atrial hypertrophy", "shortest_name_length": 18}
{"curie": "MONDO:0008339", "names": ["Webbed elbow", "Elbow webbing", "Pterygium cubitale", "Antecubital pterygium", "pterygium antecubital", "antecubital pterygium", "Pterygium, Antecubital", "PTERYGIUM, ANTECUBITAL", "pterygium, antecubital", "antecubital pterygium syndrome", "Antecubital pterygium syndrome", "Antecubital pterygium syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "antecubital pterygium syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0032627", "names": ["MC1DN23", "nuclear type mitochondrial complex I deficiency 23", "mitochondrial complex 1 deficiency, nuclear type 23", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 23"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 23", "shortest_name_length": 7}
{"curie": "MONDO:0015450", "names": ["triatrial heart", "COR TRIATRIATUM", "Cor Triatriatum", "Triatrial Heart", "Cor triatriatum", "Triatrial heart", "cor triatriatum", "Accessory atrium", "triatriatum; cor", "Heart, Triatrial", "Triatrial Hearts", "cor; triatriatum", "Hearts, Triatrial", "Subdivided Left Atrium", "Subdivided Left Atriums", "Atrium, Subdivided Left", "Left Atrium, Subdivided", "Left Atriums, Subdivided", "Atriums, Subdivided Left", "Cor Triatriatum Sinistrum", "Cor triatriatum (disorder)", "cor triatriatum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "triatrial heart", "shortest_name_length": 15}
{"curie": "MONDO:0011212", "names": ["sensorineural hearing loss, retinal pigment epithelium lesions, discolored teeth", "Sensorineural Hearing Loss, Retinal Pigment Epithelium Lesions, Discolored Teeth", "SENSORINEURAL HEARING LOSS, RETINAL PIGMENT EPITHELIUM LESIONS, DISCOLORED TEETH"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sensorineural hearing loss, retinal pigment epithelium lesions, discolored teeth", "shortest_name_length": 80}
{"curie": "UMLS:C0854791", "names": ["Bile duct cancer recurrent", "Carcinoma bile duct recurrent", "Bile duct carcinoma recurrent", "Recurrent Bile Duct Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bile duct cancer recurrent", "shortest_name_length": 26}
{"curie": "MONDO:0010434", "names": ["SS", "Synovioma", "synovioma", "Synoviomas", "Synovioma NOS", "Synovioma, NOS", "Synovial sarcoma", "synovial sarcoma", "[M]Synovioma NOS", "Synovial Sarcoma", "sarcoma synovial", "Synovialosarcoma", "SARCOMA, SYNOVIAL", "sarcoma, synovial", "Sarcoma, Synovial", "Synovial Sarcomas", "synovioma of joint", "Sarcomas, Synovial", "Malignant synovioma", "Synovioma, malignant", "Synovial sarcoma NOS", "Synovial sarcoma, NOS", "Synovial Sarcoma, NOS", "Synovial cell sarcoma", "[M]Synovial sarcoma NOS", "synovial sarcoma (disease)", "Synovial sarcoma (disorder)", "sarcoma, synovial, malignant", "synovial sarcoma (diagnosis)", "SARCOMA, SYNOVIAL, MALIGNANT", "synovioma of joint (diagnosis)", "synovial sarcoma of soft tissue", "Synovial Sarcoma, Not Otherwise Specified", "Synovial sarcoma (morphologic abnormality)", "synovial sarcoma of soft tissue (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "synovial sarcoma", "shortest_name_length": 2}
{"curie": "UMLS:C1334579", "names": ["Malignant Esophageal Neoplasm by Topographic Region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Esophageal Neoplasm by Topographic Region", "shortest_name_length": 51}
{"curie": "MONDO:0012652", "names": ["LGMD2L", "LGMDR12", "LGMD type 2L", "Anoctamin-5-related LGMD R12", "limb-girdle muscular dystrophy type 2L", "Limb-girdle muscular dystrophy type 2L", "muscular dystrophy, limb-girdle type 2L", "Muscular Dystrophy, Limb-Girdle, Type 2L", "muscular dystrophy, limb-girdle, type 2L", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L (disorder)", "muscular dystrophy, limb-girdle type 2L (diagnosis)", "Anoctamin-5-related limb-girdle muscular dystrophy R12", "ANO5 autosomal recessive limb-girdle muscular dystrophy", "muscular dystrophy, limb-girdle, autosomal recessive 12", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 12", "autosomal recessive limb-girdle muscular dystrophy type 2L", "Autosomal recessive limb-girdle muscular dystrophy type 2L", "autosomal recessive limb-girdle muscular dystrophy caused by mutation in ANO5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive limb-girdle muscular dystrophy type 2L", "shortest_name_length": 6}
{"curie": "MONDO:0004318", "names": ["Ovarian Small Cell NEC", "Ovarian Small Cell Neuroendocrine Carcinoma", "pulmonary type ovarian small cell carcinoma", "ovarian small cell carcinoma, pulmonary type", "Ovarian Small Cell Carcinoma, Pulmonary-Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary type ovarian small cell carcinoma", "shortest_name_length": 22}
{"curie": "UMLS:C0279655", "names": ["gallbladder adenoacanthoma", "adenoacanthoma of the gallbladder", "gallbladder cancer, adenoacanthoma", "gallbladder adenocarcinoma with squamous metaplasia", "Gallbladder Adenocarcinoma with Squamous Metaplasia", "Adenocarcinoma of Gallbladder with Squamous Metaplasia", "adenocarcinoma of gallbladder with squamous metaplasia", "adenocarcinoma with squamous metaplasia of the gallbladder", "Adenocarcinoma of the Gallbladder with Squamous Metaplasia", "gallbladder cancer, adenocarcinoma with squamous metaplasia", "gallbladder cancer with squamous metaplasia and adenocarcinoma", "adenocarcinoma of gallbladder with squamous metaplasia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenocarcinoma of gallbladder with squamous metaplasia", "shortest_name_length": 26}
{"curie": "UMLS:C5230988", "names": ["PNNGCT", "Non-Neural Granular Cell Tumor", "Dermal Non-Neural Granular Cell Tumor", "Primitive Polypoid Granular Cell Tumor", "Primitive non-neural granular cell tumor", "Primitive Non-Neural Granular Cell Tumor", "Primitive non-neural granular cell tumour", "Primitive non-neural granular cell tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primitive non-neural granular cell tumor", "shortest_name_length": 6}
{"curie": "MONDO:0018363", "names": ["FFDD", "focal facial dermal dysplasia", "[OBSOLETE] Focal facial dermal dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal facial dermal dysplasia", "shortest_name_length": 4}
{"curie": "MONDO:0002332", "names": ["Splenopathy", "splenopathy", "Dyssplenism", "disease spleen", "Spleen disease", "spleen disease", "Disease;spleen", "spleen diseases", "disease splenic", "Spleen Diseases", "Spleen Disorder", "DISORDER SPLEEN", "Splenic Disease", "spleen; disease", "Disorder spleen", "spleen disorder", "Splenic disease", "disorder spleen", "splenic disease", "Spleen disorder", "SPLEEN DISORDER", "Splenic Diseaess", "Disease, Splenic", "Splenic disorder", "Splenic Diseases", "Spleen Disorders", "spleen disorders", "Splenic Disorder", "Spleen--Diseases", "splenic diseases", "disorders spleen", "Spleen disorders", "splenic disorder", "Splenic diseases", "of spleen disease", "disease of spleen", "Diseases, Splenic", "splenic disorders", "disorder of spleen", "Diseases of spleen", "diseases of spleen", "Disorder of spleen", "Spleen disorder NOS", "Splenic disorder, NOS", "spleen; hyperfunction", "Splenic syndrome, NOS", "diseases of the spleen", "Disease of spleen, NOS", "DISEASES OF THE SPLEEN", "spleen disease or disorder", "Splenic disease or syndrome", "splenic disorders (diagnosis)", "Disorder of spleen (disorder)", "disease or disorder of spleen", "disease (or disorder); spleen", "Splenic Diseases and Syndromes", "Disease of spleen, unspecified", "PANHEMATOPENIA, SPLENIC PRIMARY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "splenic disorder", "shortest_name_length": 11}
{"curie": "MONDO:0003763", "names": ["Psychic shock", "psychic; shock", "Shock, psychic", "shock; psychic", "acute stress disorder", "Acute stress disorder", "Gross stress reaction", "Acute Stress Disorder", "acute stress reaction", "Acute crisis reaction", "Acute stress reaction", "crisis; acute reaction", "acute; stress reaction", "GROSS STRESS REACTIONS", "stress reaction; acute", "disorder; acute stress", "acute reaction; crisis", "Stress Disorder, Acute", "acute; stress disorder", "acute disorders stress", "Acute Stress Disorders", "Stress Disorders, Acute", "Acute reaction to stress", "acute reaction to stress", "traumatic stress disorder", "Gross stress reaction, NOS", "Reaction after;acute stress", "gross stress reaction (acute)", "Other acute reactions to stress", "acute traumatic stress disorder", "Acute stress disorder (disorder)", "acute stress disorder (diagnosis)", "Stress Disorders, Traumatic, Acute", "Trauma and Stress Related Disorders", "acute reaction to stress (diagnosis)", "trauma and stressor-related disorder", "Unspecified acute reaction to stress", "Acute reaction to stress, unspecified", "Trauma and Stressor Related Disorders", "Trauma- and stressor-related disorders", "Trauma and stressor-related disorder, NOS", "trauma and stressor-related disorder (diagnosis)", "other psychiatric disorders trauma and stressor-related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute stress disorder", "shortest_name_length": 13}
{"curie": "MONDO:0006137", "names": ["CIN 2/3", "cervical intraepithelial neoplasia grade 2/3", "Cervical Intraepithelial Neoplasia Grade 2/3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical intraepithelial neoplasia grade 2/3", "shortest_name_length": 7}
{"curie": "MONDO:0030684", "names": ["HH27", "hypogonadotropic hypogonadism 27 without anosmia", "HYPOGONADOTROPIC HYPOGONADISM 27 WITHOUT ANOSMIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadotropic hypogonadism 27 without anosmia", "shortest_name_length": 4}
{"curie": "MONDO:0012825", "names": ["EMC", "Chondroid sarcoma", "Myxoid Chondrosarcoma", "Myxoid chondrosarcoma", "Extraosseous Chondrosarcoma", "extraosseous chondrosarcoma", "extraskeletal chondrosarcoma", "Extraskeletal chondrosarcoma", "Extraskeletal Chondrosarcoma", "Extraskeletal chondrosarcomas", "Extraskeletal chondrosarcoma NOS", "myxoid extraosseous chondrosarcoma", "Myxoid Extraosseous Chondrosarcoma", "Myxoid extraosseous chondrosarcoma", "extraskeletal myxoid chondrosarcoma", "myxoid extraskeletal chondrosarcoma", "Extraskeletal myxoid chondrosarcoma", "Extraskeletal Myxoid Chondrosarcoma", "Myxoid Extraskeletal Chondrosarcoma", "CHONDROSARCOMA, EXTRASKELETAL MYXOID", "Chondrosarcoma, Extraskeletal Myxoid", "chondrosarcoma, extraskeletal myxoid", "Extraskeletal myxoid chondrosarcoma (disorder)", "Extraskeletal chondrosarcoma stage unspecified", "Extraskeletal myxoid chondrosarcoma (diagnosis)", "malignant neoplasm chondrosarcoma extraskeletal myxoid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extraskeletal myxoid chondrosarcoma", "shortest_name_length": 3}
{"curie": "UMLS:C1708783", "names": ["Lung Soft Tissue Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Soft Tissue Neoplasm", "shortest_name_length": 25}
{"curie": "UMLS:C1879351", "names": ["Jejunal obstruction", "Jejunum obstruction", "Jejunal Obstruction", "jejunum; obstruction", "obstruction; jejunum", "Jejunal obstruction (diagnosis)", "obstruction of small intestine jejunum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jejunum obstruction", "shortest_name_length": 19}
{"curie": "MONDO:0016105", "names": ["acquired skeletal muscle disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired skeletal muscle disease", "shortest_name_length": 32}
{"curie": "MONDO:0009715", "names": ["Becker Disease", "Becker disease", "BECKER DISEASE", "Disease, Becker", "generalized myotonia", "MYOTONIA, GENERALIZED", "myotonia, generalized", "Becker myotonia congenita", "Becker Generalized Myotonia", "Myotonia, Becker Generalized", "Generalized Myotonia, Becker", "myotonia congenita, recessive", "Myotonia, Generalized, Becker", "generalized myotonia was seen", "Generalized Myotonia of Becker", "Becker; recessive myotonia congenita", "Recessive form of myotonia congenita", "recessive myotonia congenita; Becker", "recessive form of congenital myotonia", "autosomal recessive myotonia congenita", "myotonia congenita, autosomal recessive", "generalized myotonia (physical finding)", "Myotonia Congenita, Autosomal Recessive", "MYOTONIA CONGENITA, AUTOSOMAL RECESSIVE", "Recessive myotonia congenita [Becker disease]", "Myotonia congenita - autosomal recessive form", "Congenital myotonia, autosomal recessive form", "recessive form of congenital myotonia (diagnosis)", "Congenital myotonia, autosomal recessive form (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myotonia congenita, autosomal recessive", "shortest_name_length": 14}
{"curie": "UMLS:C4086159", "names": ["Childhood GIST", "Gastrointestinal Stromal Tumor (GIST)", "Childhood Gastrointestinal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Gastrointestinal Stromal Tumor", "shortest_name_length": 14}
{"curie": "UMLS:C0234306", "names": ["Secondary bitter taste disorder", "Taste disorder, secondary, bitter", "Taste Disorder, Secondary, Bitter", "Secondary bitter taste disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Taste Disorder, Secondary, Bitter", "shortest_name_length": 31}
{"curie": "MONDO:0007525", "names": ["AEDS", "EDS7A", "EDS 7B", "EDS 7A", "EDS VII", "EDSARTH1", "EDS VIIA", "EDS7A (formerly)", "arthrochalasia EDS", "Ehlers-Danlos syndrome type 7", "EDS VII, Mutant Procollagen Type", "EDS VII, mutant procollagen type", "EDS VII, MUTANT PROCOLLAGEN TYPE", "Ehlers-Danlos Syndrome, Type VII", "Ehlers-Danlos syndrome, type VII", "ARTHROCHALASIS MULTIPLEX CONGENITA", "arthrochalasis multiplex congenita", "Arthrochalasis Multiplex Congenita", "arthrochalasia Ehlers-Danlos syndrome", "Ehlers-Danlos syndrome type 7A (formerly)", "Ehlers-Danlos syndrome, arthrochalasia type", "Ehlers-Danlos syndrome, arthrochalasis type", "Ehlers-Danlos Syndrome, Arthrochalasia Type", "Ehlers-Danlos syndrome arthrochalasia type 1", "Ehlers-Danlos syndrome, arthrochalasia type, 1", "EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 1", "Ehlers-Danlos syndrome, mutant procollagen type 7", "Ehlers-Danlos syndrome, autosomal dominant type 7", "Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant", "Ehlers-Danlos syndrome, type VII, autosomal dominant", "EHLERS-DANLOS SYNDROME, TYPE VIIA, AUTOSOMAL DOMINANT", "Ehlers-Danlos syndrome, type VIIA, autosomal dominant", "Ehlers-Danlos syndrome, procollagen proteinase resistant", "Ehlers-Danlos syndrome, procollagen proteinase resistant (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ehlers-Danlos syndrome, arthrochalasis type", "shortest_name_length": 4}
{"curie": "UMLS:C4764006", "names": ["MEST Family", "Kidney Mixed Epithelial and Stromal Tumor Family"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kidney Mixed Epithelial and Stromal Tumor Family", "shortest_name_length": 11}
{"curie": "MONDO:0021294", "names": ["Carcinoma in situ of cardia", "gastric cardia carcinoma in situ", "Gastric Cardia Carcinoma In Situ", "stage 0 gastric cardia carcinoma", "Stage 0 Gastric Cardia Carcinoma", "carcinoma in situ of gastric cardia", "cardia of stomach carcinoma in situ", "Carcinoma in situ of gastric cardia", "stage 0 cardia of stomach carcinoma", "cardia of stomach in situ carcinoma", "Cancer in situ of cardia of stomach", "Carcinoma in situ of Gastric Cardia", "Carcinoma in situ of cardia of stomach", "Carcinoma in situ of Cardia of Stomach", "carcinoma in situ of cardia of stomach", "carcinoma in situ of the gastric cardia", "Carcinoma in situ of the Gastric Cardia", "carcinoma in situ of the cardia of the stomach", "Carcinoma in situ of the Cardia of the Stomach", "Gastric Cardia Carcinoma In Situ AJCC v6 and v7", "gastric cardia carcinoma in situ aJCC v6 and v7", "Carcinoma in situ of cardia of stomach (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma in situ of gastric cardia", "shortest_name_length": 27}
{"curie": "MONDO:0044764", "names": ["benign choroid plexus tumor", "Benign Choroid Plexus Tumor", "benign choroid plexus tumors", "Benign Choroid Plexus Tumors", "benign tumor of choroid plexus", "Benign Choroid Plexus Neoplasm", "benign choroid plexus neoplasm", "Benign Tumor of Choroid Plexus", "Benign tumor of choroid plexus", "Benign tumour of choroid plexus", "benign choroid plexus neoplasms", "Benign Choroid Plexus Neoplasms", "benign neoplasm of choroid plexus", "Benign Neoplasm of Choroid Plexus", "benign tumor of the choroid plexus", "Benign Tumor of the Choroid Plexus", "benign neoplasm of the choroid plexus", "Benign Neoplasm of the Choroid Plexus", "Benign tumor of choroid plexus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign choroid plexus neoplasm", "shortest_name_length": 27}
{"curie": "MONDO:0011093", "names": ["MPS9", "MPS 9", "MPSIX", "MPS IX", "Hyaluronidase Deficiency", "hyaluronidase deficiency", "Hyaluronidase deficiency", "mucopolysaccharidosis IX", "HYALURONIDASE DEFICIENCY", "Deficiency of hyaluronidase", "mucopolysaccharidosis type 9", "Mucopolysaccharidosis type 9", "Mucopolysaccharidosis type IX", "Mucopolysaccharidosis Type IX", "mucopolysaccharidosis, type 9", "mucopolysaccharidosis type IX", "mucopolysaccharidosis, type IX", "MUCOPOLYSACCHARIDOSIS, TYPE IX", "Deficiency of hyaluronoglucosaminidase", "Deficiency of hyaluronoglucosaminidase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucopolysaccharidosis type 9", "shortest_name_length": 4}
{"curie": "MONDO:0013062", "names": ["LQT12", "LQT12 (diagnosis)", "Long Qt Syndrome 12", "long QT syndrome 12", "LONG QT SYNDROME 12", "SNTA1 long QT syndrome", "long QT syndrome type 12", "long QT syndrome caused by mutation in SNTA1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "long QT syndrome 12", "shortest_name_length": 5}
{"curie": "MONDO:0044800", "names": ["desmoplastic spitz nevus", "Desmoplastic spitz Nevus", "Desmoplastic Spitz nevus", "Desmoplastic Spitz Nevus", "Desmoplastic Spitz naevus", "Desmoplastic spindle and epithelioid cell nevus", "Desmoplastic spindle and epithelioid cell naevus", "Desmoplastic spindle and epithelioid cell melanocytic nevus of skin", "Desmoplastic spindle and epithelioid cell melanocytic naevus of skin", "Desmoplastic spindle and epithelioid cell melanocytic nevus of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "desmoplastic spitz nevus", "shortest_name_length": 24}
{"curie": "UMLS:C0232191", "names": ["reflex bradycardia", "Reflex bradycardia", "Reflex Bradycardia", "Reflex bradycardia (finding)", "reflex bradycardia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reflex bradycardia", "shortest_name_length": 18}
{"curie": "UMLS:C2348518", "names": ["Favorable Non-Hodgkin Lymphoma", "Favorable Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Favorable Non-Hodgkin Lymphoma", "shortest_name_length": 30}
{"curie": "UMLS:C4682575", "names": ["Stage IV Uterine Corpus Endometrial Stromal Sarcoma", "Stage IV Uterine Corpus Endometrial Stromal Sarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Uterine Corpus Endometrial Stromal Sarcoma AJCC v8", "shortest_name_length": 51}
{"curie": "MONDO:0014914", "names": ["DILOS", "DIAS-LOGAN SYNDROME", "Dias-Logan syndrome", "BCL11A-related BAFopathy", "Dias-Logan syndrome; DILOS", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN", "intellectual developmental disorder with persistence of fetal Hemoglobin", "intellectual developmental disorder with persistence of fetal HEMOGLOBIN", "Hereditary persistence of fetal hemoglobin-intellectual disability syndrome", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN", "intellectual developmental disorder with hereditary persistence of fetal Hemoglobin", "BCL11A-related intellectual developmental disorder with persistence of fetal hemoglobin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dias-Logan syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0032645", "names": ["THNS", "TRICHOHEPATONEURODEVELOPMENTAL SYNDROME", "trichohepatoneurodevelopmental syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichohepatoneurodevelopmental syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0001078", "names": ["Tropical Sprue", "sprue tropical", "Tropical sprue", "TROPICAL SPRUE", "tropical sprue", "tropical; sprue", "SPRUE, TROPICAL", "Sprue, Tropical", "sprue - tropical", "Sprue - tropical", "tropical diarrhea", "diarrhea tropical", "diarrhea; tropical", "DIARRHEA, TROPICAL", "tropical; diarrhea", "TS - Tropical sprue", "tropical steatorrhea", "tropical enteropathy", "Tropical enteropathy", "Tropical steatorrhea", "Tropical steatorrhoea", "steatorrhea; tropical", "tropical; steatorrhea", "Tropical sprue (disorder)", "tropical sprue (diagnosis)", "Tropical malabsorption syndrome", "Post-Infective Tropical Malabsorption", "post-infective tropical malabsorption", "idiopathic tropical malabsorption syndrome", "Idiopathic Tropical Malabsorption Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tropical sprue", "shortest_name_length": 14}
{"curie": "MONDO:0016264", "names": ["AIH", "Autoimmune Hepatitis", "hepatitis autoimmune", "Hepatitis autoimmune", "HEPATITIS AUTOIMMUNE", "autoimmune hepatitis", "Autoimmune hepatitis", "Hepatitis, Autoimmune", "hepatitis; autoimmune", "autoimmune; hepatitis", "HEPATITIS, AUTOIMMUNE", "Autoimmune Hepatitides", "Hepatitides, Autoimmune", "autoimmune liver disease", "chronic autoimmune hepatitis", "Chronic autoimmune hepatitis", "autoimmune chronic hepatitis", "Autoimmune Chronic Hepatitis", "Chronic Hepatitis, Autoimmune", "Hepatitis, Autoimmune Chronic", "autoimmune disorder hepatitis", "Autoimmune Chronic Hepatitides", "Hepatitides, Autoimmune Chronic", "Autoimmune hepatitis (disorder)", "Chronic Hepatitides, Autoimmune", "autoimmune hepatitis (diagnosis)", "hepatitis chronic active autoimmune", "autoimmune chronic active hepatitis", "chronic active autoimmune hepatitis", "Autoimmune chronic active hepatitis", "Chronic autoimmune hepatitis (disorder)", "chronic active autoimmune hepatitis (diagnosis)", "autoimmune hepatitis with centrilobular necrosis", "Autoimmune Hepatitis with Centrilobular Necrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune hepatitis", "shortest_name_length": 3}
{"curie": "UMLS:C0037054", "names": ["Hb-S trait", "Hb-S; trait", "trait; Hb-S", "hemoglobin; S", "S; hemoglobin", "Drepanocytosis", "drepanocytosis", "Sickle-cell trait", "trait sickle cell", "Sickle Cell Trait", "sickle cell trait", "Sickle cell trait", "Heterozygous Hb-S", "sickle-cell trait", "cell sickle trait", "SICKLE CELL TRAIT", "Sickle Cell Traits", "Cell Trait, Sickle", "trait; sickle-cell", "sickle-cell; trait", "Hemoglobin S trait", "Trait, Sickle Cell", "cells sickle trait", "sickle cell traits", "hemoglobin S trait", "Traits, Sickle Cell", "hemoglobin AS trait", "Cell Traits, Sickle", "Haemoglobin S trait", "Sickle cells present", "Heterozygous for Hb S", "sickle and cell trait", "Hemoglobin S-A disease", "AS - Sickle cell trait", "hemoglobin; AS genotype", "Hemoglobin A-S genotype", "AS genotype; hemoglobin", "hemoglobin; trait, Hb-S", "Hemoglobin S-A disorder", "Haemoglobin A-S genotype", "Haemoglobin S-A disorder", "hemoglobinopathy trait S", "hemoglobinopathy trait AS", "Heterozygous hemoglobin S", "Sickle cell trait syndrome", "Heterozygous haemoglobin S", "sickle-cell; disorder, trait", "Sickle cell trait (disorder)", "RBC's - sickle cells present", "sickle cell trait (diagnosis)", "anemia hemolytic sickle cell trait", "sickle-cell; disorder, heterozygous", "hemoglobinopathy trait S (diagnosis)", "hemoglobinopathy trait AS (diagnosis)", "hemoglobin disease; sickle-cell, trait", "sickle-cell; hemoglobin disease, trait", "disease (or disorder); sickle-cell, trait", "hemoglobin disease; sickle-cell, heterozygous", "sickle-cell; hemoglobin disease, heterozygous", "disease (or disorder); sickle-cell, heterozygous"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sickle Cell Trait", "shortest_name_length": 10}
{"curie": "MONDO:0035411", "names": ["isolated congenital hypoglossia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated congenital hypoglossia", "shortest_name_length": 31}
{"curie": "UMLS:C1336944", "names": ["Vagina Verrucous Carcinoma", "Vaginal Verrucous Carcinoma", "Verrucous Carcinoma of Vagina", "verrucous carcinoma of vagina", "Verrucous Carcinoma of the Vagina", "Vagina Verrucous Squamous Cell Carcinoma", "verrucous carcinoma of vagina (diagnosis)", "Vaginal Verrucous Squamous Cell Carcinoma", "Verrucous Squamous Cell Carcinoma of Vagina", "Verrucous Squamous Cell Carcinoma of the Vagina"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "verrucous carcinoma of vagina", "shortest_name_length": 26}
{"curie": "MONDO:0003960", "names": ["LCNEC of the lung", "LCNEC of the Lung", "Lung Large Cell Neuroendocrine Carcinoma", "lung large cell neuroendocrine carcinoma", "Large Cell Lung Neuroendocrine Carcinoma", "large cell lung neuroendocrine carcinoma", "Large Cell Neuroendocrine Carcinoma of Lung", "large cell neuroendocrine carcinoma of lung", "pulmonary large cell neuroendocrine carcinoma", "Pulmonary Large Cell Neuroendocrine Carcinoma", "Large Cell Neuroendocrine Carcinoma of the Lung", "large cell neuroendocrine carcinoma of the lung", "large cell neuroendocrine carcinoma of lung (diagnosis)", "large cell lung carcinoma with neuroendocrine differentiation", "Large Cell Lung Carcinoma with Neuroendocrine Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary large cell neuroendocrine carcinoma", "shortest_name_length": 17}
{"curie": "MONDO:0044655", "names": ["C12ORF65-related COXPD", "c12orf65-related combined oxidative phosphorylation defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "c12orf65-related combined oxidative phosphorylation defect", "shortest_name_length": 22}
{"curie": "MONDO:0001230", "names": ["acute orbital inflammation", "orbit; inflammation, acute", "Acute orbital inflammation", "inflammation; orbit, acute", "Acute inflammation of orbit", "acute inflammation of orbit", "Acute inflammation of orbit, NOS", "Acute inflammation of orbit (disorder)", "Unspecified acute inflammation of orbit", "acute inflammation of orbit (diagnosis)", "Acute inflammation of orbit, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute orbital inflammation", "shortest_name_length": 26}
{"curie": "UMLS:C0861214", "names": ["Centroblastic lymphoma refractory", "Refractory Centroblastic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Centroblastic lymphoma refractory", "shortest_name_length": 33}
{"curie": "UMLS:C5239032", "names": ["Locally Advanced Myxofibrosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Myxofibrosarcoma", "shortest_name_length": 33}
{"curie": "UMLS:C5446545", "names": ["Primary Choroidal Lymphoma", "Primary Choroidal Non-Hodgkin Lymphoma", "Choroidal Reactive Lymphoid Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Choroidal Non-Hodgkin Lymphoma", "shortest_name_length": 26}
{"curie": "MONDO:0015025", "names": ["DEE51", "EIEE51", "early infantile epileptic encephalopathy 51", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 51", "MDH2 early infantile epileptic encephalopathy", "epileptic encephalopathy, early infantile, 51", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 51", "developmental and epileptic encephalopathy 51", "developmental and epileptic encephalopathy, 51", "epileptic encephalopathy, early infantile, type 51", "epileptic encephalopathy, early infantile, 51; EIEE51", "early infantile epileptic encephalopathy caused by mutation in MDH2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 51", "shortest_name_length": 5}
{"curie": "MONDO:0008687", "names": ["Woronets trait", "WORONETS TRAIT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Woronets trait", "shortest_name_length": 14}
{"curie": "UMLS:C5670580", "names": ["Refractory Fungal Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Fungal Infection", "shortest_name_length": 27}
{"curie": "MONDO:0013284", "names": ["CVID4", "common variable immunodeficiency 4", "IMMUNODEFICIENCY, COMMON VARIABLE, 4", "immunodeficiency, common variable, 4", "antibody deficiency due to Baffr defect", "ANTIBODY DEFICIENCY DUE TO BAFFR DEFECT", "immunodeficiency, common variable, type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency, common variable, 4", "shortest_name_length": 5}
{"curie": "MONDO:0011996", "names": ["cml", "CGL", "CML", "Myelosis", "Ph1-positive CML", "Chronic myelosis", "myelosis; chronic", "chronic; myelosis", "Chronic Myeloid Leukemia", "chronic myeloid leukemia", "Chronic myeloid leukemia", "Myeloid leukemia, chronic", "myeloid leukemia, chronic", "chronic myeloid leukemias", "LEUKEMIA, CHRONIC MYELOID", "chronic myeloid leukaemia", "Leukemia, Chronic Myeloid", "Leukaemia;chronic myeloid", "leukemia, chronic myeloid", "Chronic Myeloid Leukemias", "Chronic myeloid leukaemia", "Myeloid Leukemia, chronic", "Leukemias chronic myeloid", "Myeloid Leukemia, Chronic", "LEUKEMIA, MYELOID, CHRONIC", "Leukemias, Chronic Myeloid", "Leukaemias chronic myeloid", "Leukemia, Myeloid, Chronic", "leukemia; myeloid, chronic", "Myeloid leukaemia, chronic", "Myeloid Leukemias, Chronic", "myeloid; leukemia, chronic", "Chronic Myelocytic Leukemia", "LEUKEMIA CHRONIC MYELOCYTIC", "CHRONIC MYELOCYTIC LEUKEMIA", "LEUKEMIA MYELOCYTIC CHRONIC", "chronic myelocytic leukemia", "Leukemia myelocytic chronic", "Chronic myelocytic leukemia", "Chronic Myelocytic Leukemias", "Leukemia, Chronic Myelocytic", "chronic myelogenous leukemia", "Myelocytic Leukemia, Chronic", "Chronic Myelogenous Leukemia", "Chronic myelogenous leukemia", "LEUKEMIA CHRONIC MYELOGENOUS", "Leukaemia myelocytic chronic", "myelocytic leukemia, chronic", "Chronic myelocytic leukaemia", "Leukemia, Chronic Myelogenous", "leukemia; myelocytic, chronic", "LEUKEMIA, MYELOCYTIC, CHRONIC", "chronic myelogenous leukaemia", "Ph1-Positive Myeloid Leukemia", "leukemia, chronic myelogenous", "Myelocytic Leukemias, Chronic", "Leukemias, Chronic Myelocytic", "chronic granulocytic leukemia", "Chronic granulocytic leukemia", "CML - Philadelphia chromosome", "myelocytic; leukemia, chronic", "Chronic Granulocytic Leukemia", "CHRONIC GRANULOCYTIC LEUKEMIA", "myelogenous leukemia, chronic", "Chronic Myelogenous Leukemias", "chronic myelogenous leukemias", "Myelogenous Leukemia, Chronic", "Leukemia, Myelocytic, Chronic", "LEUKEMIA, CHRONIC MYELOGENOUS", "Chronic myelogenous leukaemia", "Leukemias, Chronic Myelogenous", "Myelogenous Leukemias, Chronic", "Chronic Granulocytic Leukemias", "chronic granulocytic leukaemia", "Chronic granulocytic leukaemia", "Myeloid Leukemia, Ph1 Positive", "LEUKEMIA, MYELOGENOUS, CHRONIC", "Ph1-Positive Myeloid Leukemias", "granulocytic leukemia, chronic", "Leukemia, Chronic Granulocytic", "Leukemia, Ph1-Positive Myeloid", "Leukemia, Myelogenous, Chronic", "Myeloid Leukemia, Ph1-Positive", "CML - Chronic myeloid leukemia", "Granulocytic Leukemia, Chronic", "Leukemia, Myeloid, Ph1 Positive", "leukemia; granulocytic, chronic", "Granulocytic Leukemias, Chronic", "CML - Chronic myeloid leukaemia", "Leukemias, Chronic Granulocytic", "Myeloid Leukemias, Ph1-Positive", "Leukemias, Ph1-Positive Myeloid", "granulocytic; leukemia, chronic", "LEUKEMIA, GRANULOCYTIC, CHRONIC", "Leukemia, Granulocytic, Chronic", "Leukemia, Myeloid, Ph1-Positive", "Chronic myeloid leukemia, disease", "Ph1-Positive Myelogenous Leukemia", "Chronic Myelogenous Leukemia (CML)", "CML - Chronic Myelogenous Leukemia", "Chronic myeloid leukaemia, disease", "Leukemia, myelomonocytic (Naegeli)", "Myelogenous Leukemia, Ph1-Positive", "CML - chronic Myelogenous Leukemia", "Leukemia, Ph1-Positive Myelogenous", "Ph1-Positive Myelogenous Leukemias", "CML (chronic myelogenous leukemia)", "chronic myelogenous leukemia (CML)", "Myelogenous Leukemia, Ph1 Positive", "Chronic myelogenous leukemia (CML)", "CML - chronic myelogenous leukemia", "Leukemia, Myelogenous, Ph1-Positive", "CGL - Chronic granulocytic leukemia", "Myelogenous Leukemias, Ph1-Positive", "Leukemia, Myelogenous, Ph1 Positive", "Leukemias, Ph1-Positive Myelogenous", "leukemia, chronic myeloid, atypical", "Philadelphia Chromosome Positive CML", "CGL - Chronic granulocytic leukaemia", "Philadelphia chromosome-positive CML", "CML, Philadelphia chromosome-positive", "CGL, Philadelphia chromosome-positive", "Chronic granulocytic leukemia, BCR/ABL", "Philadelphia-Positive Myeloid Leukemia", "Chronic granulocytic leukaemia, BCR/ABL", "Leukemia, Philadelphia-Positive Myeloid", "Myeloid Leukemia, Philadelphia-Positive", "Myeloid Leukemia, Philadelphia Positive", "Philadelphia-Positive Myeloid Leukemias", "Myeloid Leukemias, Philadelphia-Positive", "chronic myelogenous leukemia (diagnosis)", "Leukemia, Myeloid, Philadelphia-Positive", "Leukemias, Philadelphia-Positive Myeloid", "Leukemia, Myeloid, Philadelphia Positive", "Ph1-positive chronic myelogenous leukemia", "Ph1-positive chronic granulocytic leukemia", "Ph1 Positive Chronic Granulocytic Leukemia", "Ph' Positive Chronic Granulocytic Leukemia", "Chronic myeloid leukemia, disease (disorder)", "chronic myelogenous leukemia BCR/ABL positive", "BCR-ABL Positive chronic myelogenous leukemia", "BCR-ABL Positive Chronic Myelogenous Leukemia", "Chronic myelogenous leukemia, BCR/ABL positive", "Chronic myelogenous leukemia, t(9;22)(q34;q11)", "Chronic myelogenous leukemia, BCR-ABL positive", "chronic myelogenous leukemia - BCR/ABL positive", "Chronic myelogenous leukemia, t(9;22) (q34;q11)", "Chronic Myelogenous Leukemia, BCR-ABL1 Positive", "Chronic myelogenous leukaemia, t(9;22)(q34;q11)", "Chronic myelogenous leukaemia, BCR/ABL positive", "chronic myelogenous leukemia, BCR-ABL1 Positive", "chronic myelogenous leukemia, BCR-ABL1 positive", "Chronic granulocytic leukemia, t(9;22)(q34;q11)", "Chronic granulocytic leukaemia, t(9;22)(q34;q11)", "Ph1 chromosome-positive chronic myeloid leukemia", "Ph' Chromosome Positive Chronic Myeloid Leukemia", "Ph1 Chromosome Positive Chronic Myeloid Leukemia", "Leukemia, Myelogenous, Chronic, BCR-ABL Positive", "Hematopoeitic - Chronic Myelocytic Leukemia (CML)", "hematopoeitic - chronic myelocytic leukemia (CML)", "Chronic myeloid leukemia (morphologic abnormality)", "Ph1 Chromosome Positive Chronic Myelocytic Leukemia", "Ph1 chromosome-positive chronic myelocytic leukemia", "Ph' Chromosome Positive Chronic Myelocytic Leukemia", "Ph1 Chromosome Positive Chronic Myelogenous Leukemia", "Ph1 chromosome-positive chronic myelogenous leukemia", "Ph' Chromosome Positive Chronic Myelogenous Leukemia", "Philadelphia Chromosome Positive Chronic Myeloid Leukemia", "Philadelphia chromosome-positive chronic myeloid leukemia", "chronic myelogenous leukemia - BCR/ABL positive (diagnosis)", "chronic myeloid leukemia t(9;22) (q34;q11), BCR/ABL positive", "Philadelphia chromosome-positive chronic myelocytic leukemia", "Philadelphia Chromosome Positive Chronic Myelocytic Leukemia", "Chronic Myeloid Leukemia t(9;22) (q34;q11), BCR/ABL Positive", "Philadelphia chromosome positive chronic myelogenous leukemia", "Philadelphia Chromosome Positive Chronic Myelogenous Leukemia", "chronic myelocytic leukemia, Philadelphia chromosome-positive", "Chronic myelogenous leukemia, Philadelphia chromosome positive", "chronic myelogenous leukemia, Philadelphia chromosome-positive", "myelocytic leukemia, chronic, Philadelphia chromosome-positive", "Philadelphia chromosome positive chronic myelogenous leukaemia", "Philadelphia Chromosome Positive Chronic Granulocytic Leukemia", "Philadelphia chromosome positive chronic granulocytic leukemia", "chronic granulocytic leukemia, Philadelphia chromosome-positive", "myelogenous leukemia, chronic, Philadelphia chromosome-positive", "granulocytic leukemia, chronic, Philadelphia chromosome-positive", "LEUKEMIA, PHILADELPHIA CHROMOSOME-POSITIVE, RESISTANT TO IMATANIB", "Chronic myelogenous leukemia, Philadelphia chromosome (Ph1) positive", "leukemia, chronic myeloid, Philadelphia chromosome positive, somatic", "Chronic myelogenous leukaemia, Philadelphia chromosome (Ph1) positive", "Chronic granulocytic leukemia, Philadelphia chromosome (Ph1) positive", "Chronic myelogenous leukemia, Philadelphia chromosome (Ph 1) positive", "Chronic granulocytic leukaemia, Philadelphia chromosome (Ph1) positive", "Chronic myelogenous leukemia, BCR/ABL positive (morphologic abnormality)", "Philadelphia chromosome positive chronic myelogenous leukemia (disorder)", "Philadelphia chromosome positive chronic myelogenous leukemia (diagnosis)", "Philadelphia Chromosome Positive, BCR-ABL1 Positive Chronic Myelogenous Leukemia", "leukemia, Philadelphia chromosome-positive, resistant to imatinib, Somatic mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic myelogenous leukemia, BCR-ABL1 positive", "shortest_name_length": 3}
{"curie": "MONDO:0010326", "names": ["MRX46", "XLID46", "X-linked mental retardation 46", "Mental Retardation, X-Linked 46", "MENTAL RETARDATION, X-LINKED 46", "mental retardation, X-linked 46", "intellectual disability, X-linked 46", "mental retardation, X-linked type 46", "intellectual disability, X-linked type 46", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 46", "non-syndromic X-linked intellectual disability 46", "mental retardation, X-linked 46, X-linked recessive", "ARHGEF6 non-syndromic X-linked intellectual disability", "non-syndromic X-linked intellectual disability caused by mutation in ARHGEF6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 46", "shortest_name_length": 5}
{"curie": "UMLS:C1096045", "names": ["Human immunodeficiency virus transmission"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Human immunodeficiency virus transmission", "shortest_name_length": 41}
{"curie": "MONDO:0017431", "names": ["limb overgrowth", "non-syndromic limb overgrowth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-syndromic limb overgrowth", "shortest_name_length": 15}
{"curie": "UMLS:C5418816", "names": ["Recurrent Malignant Mastocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Malignant Mastocytosis", "shortest_name_length": 32}
{"curie": "UMLS:C5669729", "names": ["Recurrent Hormone Receptor Positive Breast Carcinoma", "Recurrent Hormone Receptor-Positive Breast Carcinoma", "Recurrent Hormone Receptor Positive Breast Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Hormone Receptor-Positive Breast Carcinoma", "shortest_name_length": 52}
{"curie": "UMLS:C0271819", "names": ["Hurthle cell metaplasia of thyroid", "Hurthle cell metaplasia of thyroid gland", "Hurthle Cell Metaplasia of Thyroid Gland", "Hurthle cell metaplasia of thyroid gland (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hurthle cell metaplasia of thyroid gland", "shortest_name_length": 34}
{"curie": "UMLS:C0349749", "names": ["Lacrimal Duct Neoplasm", "Lacrimal duct neoplasm", "Neoplasm of lacrimal duct", "Nasolacrimal Duct Neoplasm", "Neoplasm of nasolacrimal duct", "eye neoplasm nasolacrimal duct", "Tumor of lacrimal drainage structure", "Tumour of lacrimal drainage structure", "Neoplasm of nasolacrimal duct (disorder)", "Neoplasm of nasolacrimal duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplasm of lacrimal duct", "shortest_name_length": 22}
{"curie": "UMLS:C4525616", "names": ["Stage II Duodenal Neuroendocrine Tumor", "Stage II Duodenal Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Duodenal Neuroendocrine Tumor AJCC v8", "shortest_name_length": 38}
{"curie": "UMLS:C1706831", "names": ["Appendix MANEC", "Appendix Mixed Endocrine-Exocrine Neoplasm", "Appendix Mixed Adenoneuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Appendix Mixed Adenoneuroendocrine Carcinoma", "shortest_name_length": 14}
{"curie": "MONDO:0024652", "names": ["Cyst of mesenteric remnant", "cyst of mesenteric remnant", "embryonal; cyst fallopian tube", "cyst; embryonal, fallopian tube", "embryonic cyst of fallopian tube", "Embryonic cyst of fallopian tube", "Congenital cyst of fallopian tube", "Embryonic cyst of fallopian tube (disorder)", "embryonic cyst of fallopian tube (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "embryonic cyst of fallopian tube", "shortest_name_length": 26}
{"curie": "UMLS:C1336454", "names": ["stage I extragonadal seminoma", "Stage I Extragonadal Seminoma", "Stage I Extragonadal Primary Seminoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Extragonadal Seminoma", "shortest_name_length": 29}
{"curie": "UMLS:C5239115", "names": ["Advanced HER2-Negative Breast Carcinoma", "Advanced HER2 Negative Breast Carcinoma", "Advanced HER2 Negative Breast Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced HER2-Negative Breast Carcinoma", "shortest_name_length": 39}
{"curie": "UMLS:C1334415", "names": ["Low Grade Gastric Intraepithelial Neoplasia", "Gastric Mild Intraepithelial Neoplasia (Dysplasia)", "Low-Grade Gastric Glandular Intraepithelial Neoplasia", "Low Grade Gastric Intraepithelial Neoplasia (Dysplasia)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Grade Gastric Intraepithelial Neoplasia", "shortest_name_length": 43}
{"curie": "MONDO:0007111", "names": ["ANIB1", "intracranial berry aneurysm 1", "aneurysm, intracranial berry, 1", "ANEURYSM, INTRACRANIAL BERRY, 1", "Aneurysm, Intracranial Berry, 1", "aneurysm, intracranial berry type 1", "Aneurysmal Subarachnoid Hemorrhage, Familial", "ANEURYSMAL SUBARACHNOID HEMORRHAGE, FAMILIAL", "aneurysmal subarachnoid hemorrhage, familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aneurysm, intracranial berry type 1", "shortest_name_length": 5}
{"curie": "MONDO:0013545", "names": ["ATFB12", "atrial fibrillation familial 12", "ATRIAL FIBRILLATION, FAMILIAL, 12", "atrial fibrillation, familial, 12", "ABCC9 familial atrial fibrillation", "atrial fibrillation, familial, type 12", "atrial fibrillation familial 12 (diagnosis)", "familial atrial fibrillation caused by mutation in ABCC9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial fibrillation, familial, 12", "shortest_name_length": 6}
{"curie": "EFO:1001253", "names": ["maculopapular eruption"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maculopapular eruption", "shortest_name_length": 22}
{"curie": "MONDO:0014102", "names": ["HH17", "SPRY4 hypogonadotropic hypogonadism", "hypogonadotropic hypogonadism 17 with or without anosmia", "HYPOGONADOTROPIC HYPOGONADISM 17 WITH OR WITHOUT ANOSMIA", "hypogonadotropic hypogonadism caused by mutation in SPRY4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadotropic hypogonadism 17 with or without anosmia", "shortest_name_length": 4}
{"curie": "UMLS:C5555773", "names": ["Peritoneal Endometrioid Stromal Sarcoma", "Peritoneal Low Grade Endometrioid Stromal Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peritoneal Low Grade Endometrioid Stromal Sarcoma", "shortest_name_length": 39}
{"curie": "MONDO:0100489", "names": ["GRD", "GRD1", "GRAVES DISEASE, SUSCEPTIBILITY TO, 1", "Graves disease, susceptibility to, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Graves disease, susceptibility to, 1", "shortest_name_length": 3}
{"curie": "MONDO:0021130", "names": ["disorder of sphingolipid biosynthesis", "inborn sphingolipid biosynthetic process disorder", "inborn error of sphingolipid biosynthetic process", "rare inborn error of sphingolipid biosynthetic process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of sphingolipid biosynthesis", "shortest_name_length": 37}
{"curie": "MONDO:0016302", "names": ["isolated congenitally uncorrected transposition of the great vessels", "isolated congenitally uncorrected transposition of the great arteries"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated congenitally uncorrected transposition of the great arteries", "shortest_name_length": 68}
{"curie": "MONDO:0005204", "names": ["primary antiphospholipid syndrome", "Primary antiphospholipid syndrome", "antiphospholipid antibody syndrome primary", "Primary antiphospholipid syndrome (disorder)", "Primary antiphospholipid syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary antiphospholipid syndrome", "shortest_name_length": 33}
{"curie": "MONDO:0018686", "names": ["Acquired CJD", "acquired CJD", "sporadic CJD", "acquired Creutzfeldt Jacob disease", "acquired Creutzfeldt-Jakob disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired Creutzfeldt-Jakob disease", "shortest_name_length": 12}
{"curie": "UMLS:C5237207", "names": ["Skin Squamous Cell Carcinoma with Osteoclast-Like Giant Cells"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin Squamous Cell Carcinoma with Osteoclast-Like Giant Cells", "shortest_name_length": 61}
{"curie": "MONDO:0014144", "names": ["LGMD2S", "LGMDR18", "LGMD type 2S", "TRAPPC11-related LGMD R18", "Limb-girdle muscular dystrophy type 2S", "limb-girdle muscular dystrophy type 2S", "muscular dystrophy, limb-girdle type 2S", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S", "muscular dystrophy, limb-girdle, type 2S", "TRAPPC11-related limb-girdle muscular dystrophy R18", "muscular dystrophy, limb-girdle type 2S (diagnosis)", "progressive muscular dystrophy - limb girdle - type 2s", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 18", "muscular dystrophy, limb-girdle, autosomal recessive 18", "Autosomal recessive limb girdle muscular dystrophy type 2S", "autosomal recessive limb-girdle muscular dystrophy type 2S", "Autosomal recessive limb-girdle muscular dystrophy type 2S", "TRAPPC11 autosomal recessive limb-girdle muscular dystrophy", "autosomal recessive limb-girdle muscular dystrophy type R18", "Autosomal recessive limb girdle muscular dystrophy type 2S (disorder)", "autosomal recessive limb-girdle muscular dystrophy caused by mutation in TRAPPC11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive limb-girdle muscular dystrophy type R18", "shortest_name_length": 6}
{"curie": "UMLS:C1536561", "names": ["Ancient schwannoma", "Ancient Schwannoma", "Ancient neurilemoma", "Ancient neurilemmoma", "Ancient Neurilemmoma", "Degenerated schwannoma", "Degenerated Schwannoma", "Degenerated Neurilemmoma", "Ancient schwannoma (disorder)", "Ancient schwannoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Degenerated Schwannoma", "shortest_name_length": 18}
{"curie": "MONDO:0017430", "names": ["congenital joint dislocations", "non-syndromic congenital joint dislocations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-syndromic congenital joint dislocations", "shortest_name_length": 29}
{"curie": "MONDO:0008433", "names": ["sclc", "SCLC", "SCCL", "SCLC1", "Small Cell NEC", "oat cell cancer", "Small Cell Cancer", "Oat cell carcinoma", "oat cell carcinoma", "Oat Cell Carcinoma", "Carcinoma, Oat Cell", "Oat Cell Carcinomas", "small cell carcinoma", "Small Cell Carcinoma", "SMALL CELL CARCINOMA", "Round cell carcinoma", "Small cell carcinoma", "cancer cell lung oat", "lung cancer oat cell", "Carcinomas, Oat Cell", "oat cell lung cancer", "Oat cell lung cancer", "Oat Cell Lung Cancer", "Small Cell Carcinomas", "Carcinoma, Small Cell", "Small cell lung cancer", "Small Cell Lung Cancer", "LUNG CANCER SMALL CELL", "Reserve cell carcinoma", "Carcinomas, Small Cell", "cancer cell lung small", "small cell lung cancer", "Lung cancer, small cell", "lung oat cell carcinoma", "oat cell lung carcinoma", "Oat Cell Lung Carcinoma", "lung cancer, small cell", "Lung Oat Cell Carcinoma", "Small cell carcinoma NOS", "LUNG CARCINOMA, OAT CELL", "Small cell lung carcinoma", "lung small cell carcinoma", "Small Cell Lung Carcinoma", "small-cell cancer of lung", "small cell lung carcinoma", "Small cell carcinoma, NOS", "Lung Small Cell Carcinoma", "oat cell carcinoma of lung", "Carcinoma, Small Cell Lung", "Oat cell carcinoma of lung", "OAT CELL CARCINOMA OF LUNG", "Oat Cell Carcinoma of Lung", "SCC - Small cell carcinoma", "LUNG CARCINOMA, SMALL CELL", "Oat cell carcinoma syndrome", "Small cell carcinoma of lung", "small cell carcinoma of lung", "SMALL CELL CARCINOMA OF LUNG", "Small Cell Carcinoma of Lung", "Small Cell Cancer Of The Lung", "small cell cancer of the lung", "SMALL CELL CANCER OF THE LUNG", "SCLC - Small cell lung cancer", "small cell lung cancer (SCLC)", "oat cell carcinoma of the lung", "Oat Cell Carcinoma of the Lung", "Small cell carcinoma (disorder)", "small cell carcinoma of the lung", "Small Cell Carcinoma of the Lung", "small cell carcinoma (diagnosis)", "Small cell carcinoma of the lung", "lung malignant carcinoma oat cell", "LUNG CANCER, SMALL CELL CARCINOMA", "Small cell lung cancer progression", "Small Cell Neuroendocrine Carcinoma", "Small cell neuroendocrine carcinoma", "Oat cell carcinoma of lung (disorder)", "small cell cancer of the lung, somatic", "Small cell carcinoma of lung (disorder)", "PULMONARY SMALL CELL CARCINOMA OAT CELL", "Small cell lung cancer stage unspecified", "poorly differentiated endocrine neoplasm", "small cell carcinoma of lung (diagnosis)", "Lung Small Cell Neuroendocrine Carcinoma", "lung small cell neuroendocrine carcinoma", "PULMONARY SMALL CELL CARCINOMA <OAT CELL>", "small cell neuroendocrine carcinoma of lung", "Small Cell Neuroendocrine Carcinoma of Lung", "Oat cell carcinoma (morphologic abnormality)", "oat cell carcinoma (morphologic abnormality)", "lung malignant carcinoma oat cell (diagnosis)", "Small cell carcinoma (morphologic abnormality)", "Small Cell Neuroendocrine Carcinoma of the Lung", "small cell neuroendocrine carcinoma of the lung", "Small cell neuroendocrine carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small cell lung carcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0015449", "names": ["crisscross heart", "Crisscross Heart", "Crisscross heart", "Criss cross Heart", "criss cross heart", "Criss-cross Heart", "Criss-cross heart", "Heart, Crisscross", "criss-cross heart", "Crisscross Hearts", "Hearts, Crisscross", "Criss-cross Hearts", "Heart, Criss-cross", "Hearts, Criss-cross", "superoinferior ventricles", "Superoinferior ventricles", "Criss-cross heart (disorder)", "twisted atrioventricular connections", "Twisted atrioventricular connections", "criss-cross atrioventricular relationship", "Criss-cross atrioventricular relationships", "criss-cross atrioventricular relationships", "criss-cross atrioventricular relationship (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "criss-cross heart", "shortest_name_length": 16}
{"curie": "UMLS:C4524724", "names": ["Pathologic Stage 0 Gastroesophageal Junction Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage 0 Gastroesophageal Junction Adenocarcinoma AJCC v8", "shortest_name_length": 67}
{"curie": "MONDO:0002114", "names": ["pancreas lymphoma", "pancreatic lymphoma", "Pancreatic Lymphoma", "Lymphoma of Pancreas", "lymphoma of pancreas", "Lymphoma of pancreas", "Lymphoma of the Pancreas", "lymphoma of the pancreas", "malignant lymphoma of pancreatic lymph nodes", "malignant lymphoma of pancreatic lymph nodes (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreas lymphoma", "shortest_name_length": 17}
{"curie": "UMLS:C1881059", "names": ["Hodgkin's Disease, Lymphocyte Depletion, Reticular"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's Disease, Lymphocyte Depletion, Reticular", "shortest_name_length": 50}
{"curie": "MONDO:8000023", "names": ["ALPS-U", "Type 3 ALPS", "type 3 autoimmune lymphoproliferative syndrome", "Type 3 Autoimmune Lymphoproliferative Syndrome", "Autoimmune Lymphoproliferative Syndrome-Undetermined variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type 3 autoimmune lymphoproliferative syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0700144", "names": ["Canine Leukemia", "canine leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canine leukemia", "shortest_name_length": 15}
{"curie": "UMLS:C1332890", "names": ["CNS Paraganglioma", "Paraganglioma of CNS", "Paraganglioma of the CNS", "Central Nervous System Paraganglioma", "Paraganglioma of Central Nervous System", "Paraganglioma of the Central Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Paraganglioma", "shortest_name_length": 17}
{"curie": "UMLS:C1333275", "names": ["Skin Fibroma", "Skin fibromas", "Dermal Fibroma", "Fibroma of Skin", "Fibroma of the Skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dermal Fibroma", "shortest_name_length": 12}
{"curie": "MONDO:0015587", "names": ["rolandic epilepsy-speech dyspraxia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rolandic epilepsy-speech dyspraxia syndrome", "shortest_name_length": 43}
{"curie": "UMLS:C4763550", "names": ["Advanced Extracranial Malignant Solid Tumor", "Advanced Extracranial Malignant Solid Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Extracranial Malignant Solid Neoplasm", "shortest_name_length": 43}
{"curie": "MONDO:0004261", "names": ["periductal breast myoepitheliosis", "Breast Periductal Myoepitheliosis", "Periductal Breast Myoepitheliosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "periductal breast myoepitheliosis", "shortest_name_length": 33}
{"curie": "MONDO:0008401", "names": ["Psa", "PSA", "SGPA", "Sgpa", "tumor mix", "tumour mix", "mixed tumor", "Mixed tumor", "Mixed tumour", "mixed tumors", "Mixed tumor, NOS", "Mixed tumour, NOS", "Chondroid Syringoma", "Pleomorphic Adenoma", "Pleomorphic adenoma", "chondroid syringoma", "pleomorphic adenoma", "adenoma pleomorphic", "Chondroid syringoma", "pleomorphic adenomas", "chondroid; syringoma", "Adenoma, Pleomorphic", "tumor, mixed, benign", "Chondroid Syringomas", "Pleomorphic Adenomas", "TUMOR, MIXED, BENIGN", "Syringoma, Chondroid", "syringoma; chondroid", "Syringomas, Chondroid", "Adenomas, Pleomorphic", "Mixed Salivary Gland Tumor", "Mixed salivary gland tumor", "Mixed salivary gland tumour", "Salivary Gland Tumor, Mixed", "Benign Mixed Salivary Tumor", "Mixed Tumor of Salivary Gland", "Benign Mixed Salivary Neoplasm", "Mixed tumor, salivary gland type", "Mixed Tumor of the Salivary Gland", "Mixed tumour, salivary gland type", "mixed tumor of the Salivary gland", "Benign Mixed Salivary Gland Tumor", "mixed tumor of the salivary gland", "Pleomorphic salivary gland adenoma", "pleomorphic salivary gland adenoma", "Salivary Gland Pleomorphic Adenoma", "SALIVARY GLAND ADENOMA, PLEOMORPHIC", "salivary gland adenoma, pleomorphic", "Salivary Gland Adenoma, Pleomorphic", "Benign Mixed Salivary Gland Neoplasm", "Pleomorphic adenoma of salivary gland", "Mixed tumor, salivary gland type, NOS", "pleomorphic adenoma of salivary gland", "Mixed tumour, salivary gland type, NOS", "adenomas, salivary gland pleomorphic, somatic", "pleomorphic adenoma (morphologic abnormality)", "Pleomorphic adenoma (morphologic abnormality)", "Pleomorphic adenoma of salivary gland (disorder)", "pleomorphic adenoma of salivary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pleomorphic adenoma", "shortest_name_length": 3}
{"curie": "MONDO:0000079", "names": ["hypophosphatemic nephrolithiasis/osteoporosis", "nephrolithiasis/osteoporosis, hypophosphatemic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrolithiasis/osteoporosis, hypophosphatemic", "shortest_name_length": 45}
{"curie": "UMLS:C1444066", "names": ["Encapsulated tumor", "Encapsulated tumour", "Encapsulated Neoplasm", "Tumor contained within organ capsule", "Tumour contained within organ capsule", "Tumor contained within organ capsule (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tumor contained within organ capsule", "shortest_name_length": 18}
{"curie": "UMLS:C4287828", "names": ["Ovarian Cancer by AJCC v6 and v7 Stage", "Ovarian Carcinoma by AJCC v6 and v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Cancer by AJCC v6 and v7 Stage", "shortest_name_length": 38}
{"curie": "MONDO:0005665", "names": ["Bell palsy", "Bell Palsy", "bell palsy", "Bells Palsy", "Palsy;Bells", "Bell; palsy", "bells palsy", "palsy bells", "palsy; Bell", "Palsy, Bell", "Palsy Bells", "PALSY BELLS", "Bells palsy", "BELL'S PALSY", "facial palsy", "Facial Palsy", "Bell's Palsy", "Bell Palsies", "bell's palsy", "Bell's palsy", "Facial palsy", "Palsies, Bell", "Palsy, Bell's", "bells's palsy", "Bell's Palsies", "Bell; paralysis", "paralysis; Bell", "Palsies, Bell's", "BELL'S PARALYSIS", "Facial Paralysis", "facial nerve palsy", "Facial nerve palsy", "Facial Nerve Palsy", "palsy of facial nerve", "Bell's (facial) palsy", "Facial Nerve Paralysis", "Facial nerve paralysis", "facial nerve paralysis", "Cranial nerve VII palsy", "Cranial nerve palsy VII", "Bell's palsy (disorder)", "Cranial Nerve VII Palsy", "paralysis; Bell's palsy", "Bell's palsy; paralysis", "nerve paralysis, Facial", "Bell's palsy (diagnosis)", "paralysis Of Facial nerve", "VII th cranial nerve palsy", "Idiopathic Facial Paralyses", "IDIOPATHIC FACIAL PARALYSIS", "Seventh cranial nerve palsy", "Idiopathic Facial Paralysis", "Paralysis, Idiopathic Facial", "Facial paralysis/Bells palsy", "Facial Paralyses, Idiopathic", "Facial Paralysis, Idiopathic", "Paralyses, Idiopathic Facial", "facial paralysis bell's palsy", "bell's palsy facial paralysis", "Facial paralysis/bell's palsy", "Idiopathic Acute Facial Neuropathy", "Acute Idiopathic Facial Neuropathy", "Facial Neuropathy, Idiopathic Acute", "Idiopathic acute facial nerve palsy", "Acute Inflammatory Facial Neuropathy", "Facial palsy, unilateral or bilateral", "Inflammatory Facial Neuropathy, Acute", "Facial Neuropathy, Inflammatory, Acute", "Facial muscle weakness of muscles innervated by CN VII"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bell's palsy", "shortest_name_length": 10}
{"curie": "UMLS:C5420533", "names": ["Unresectable Cervical Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Cervical Adenocarcinoma", "shortest_name_length": 36}
{"curie": "MONDO:0006001", "names": ["endemic; hematuria", "HEMATURIA, ENDEMIC", "hematuria; endemic", "Bilharzial cystitis", "Bilharzia infection", "bladder schistosomiasis", "Schistosomiasis bladder", "Urinary Schistosomiases", "Vesical schistosomiasis", "Schistosoma; hematobium", "bladder Schistosomiasis", "Bladder Schistosomiasis", "vesical schistosomiasis", "urinary schistosomiasis", "schistosomiasis urinary", "Urinary schistosomiasis", "Schistosoma haematobium", "Bladder schistosomiasis", "Urinary Schistosomiasis", "Schistosoma; haematobium", "Schistosomiasis, Urinary", "Schistosomiases, Urinary", "Urogenital Schistosomiases", "cystitis with bilharziasis", "Schistosomiasis haematobia", "schistosomiasis of bladder", "schistosomiasis haematobia", "Urogenital Schistosomiasis", "Schistosomiasis of bladder", "Cystitis with bilharziasis", "SCHISTOSOMIASIS HAEMATOBIA", "Vesical schistosomiasis NOS", "Schistosomiases, Urogenital", "Schistosomiasis haematobium", "Schistosomiasis, Urogenital", "urinary bladder schistosomiasis", "Schistosoma Hematobium Infection", "Schistosoma hematobium infection", "Schistosoma haematobia Infection", "Schistosoma haematobia Infections", "Schistosoma haematobium infection", "Infection, Schistosoma haematobia", "Urinary schistosomiasis (disorder)", "Infections, Schistosoma haematobia", "bladder; schistosomiasis (etiology)", "Urinary schistosomiasis (diagnosis)", "schistosomiasis; bladder (etiology)", "Cystitis with bilharziasis (disorder)", "cystitis with bilharziasis (diagnosis)", "schistosomiasis; Schistosoma hematobium", "schistosomiasis; bladder (manifestation)", "schistosomiasis; Schistosoma haematobium", "bladder; schistosomiasis (manifestation)", "Schistosoma hematobium infectious disease", "Schistosoma haematobium infection (disorder)", "Schistosomiasis due to schistosoma hematobium", "schistosomiasis due to Schistosoma haematobium", "Schistosomiasis due to schistosoma haematobium", "Schistosoma haematobium (& vesical schistosomiasis)", "bladder; disorder, in schistosomiasis (bilharziasis) (etiology)", "bladder; disorder, in schistosomiasis (bilharziasis) (manifestation)", "Schistosomiasis due to Schistosoma hematobium [urinary schistosomiasis]", "Schistosomiasis due to Schistosoma haematobium [urinary schistosomiasis]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urinary schistosomiasis", "shortest_name_length": 18}
{"curie": "MONDO:0004703", "names": ["Bladder Flat CIS", "bladder flat CIS", "Bladder Ca in situ", "bladder Ca in situ", "flat CIS of the bladder", "Flat CIS of the Bladder", "urinary bladder flat CIS", "stage 0is bladder cancer", "Stage 0is Bladder Cancer", "Urinary Bladder Flat CIS", "bladder carcinoma in situ", "stage 0is bladder carcinoma", "Stage 0is Bladder Carcinoma", "carcinoma in situ of bladder", "Carcinoma in situ of bladder", "stage 0is carcinoma of bladder", "Bladder Flat Carcinoma in Situ", "Stage 0is Carcinoma of Bladder", "bladder flat carcinoma in situ", "flat CIS of the urinary bladder", "Flat CIS of the urinary bladder", "Flat CIS of the Urinary Bladder", "Carcinoma in situ of bladder NOS", "Carcinoma in situ of the bladder", "Cancer in situ of urinary bladder", "urinary bladder carcinoma in situ", "urinary bladder in situ carcinoma", "stage 0 urinary bladder carcinoma", "Carcinoma in situ of bladder, NOS", "cancer in situ of urinary bladder", "Stage 0is Carcinoma of the Bladder", "CIS - Carcinoma in situ of bladder", "stage 0is carcinoma of the bladder", "stage 0is bladder urothelial cancer", "Stage 0is Urinary Bladder Carcinoma", "stage 0is urinary bladder carcinoma", "Stage 0is Bladder Urothelial Cancer", "carcinoma in situ of urinary bladder", "Carcinoma in situ of Urinary Bladder", "flat carcinoma in situ of the bladder", "Flat Carcinoma in Situ of the Bladder", "stage 0is carcinoma of urinary bladder", "stage 0is bladder urothelial carcinoma", "Stage 0is Carcinoma of Urinary Bladder", "urinary bladder flat carcinoma in situ", "Stage 0is Bladder Urothelial Carcinoma", "Urinary Bladder Flat Carcinoma in Situ", "Carcinoma in situ of bladder (disorder)", "carcinoma in situ of bladder (diagnosis)", "carcinoma in situ of the urinary bladder", "Carcinoma in situ of the Urinary Bladder", "stage 0is carcinoma of the urinary bladder", "Stage 0is Carcinoma of the Urinary Bladder", "high grade bladder Intraurothelial neoplasia", "High Grade Bladder Intraurothelial Neoplasia", "Flat Carcinoma in Situ of the Urinary Bladder", "flat carcinoma in situ of the urinary bladder", "stage 0is bladder urothelial carcinoma aJCC v6", "stage 0is bladder urothelial carcinoma aJCC v7", "Stage 0is Bladder Urothelial Carcinoma AJCC v7", "Stage 0is Bladder Urothelial Carcinoma AJCC v6", "Stage 0is Bladder Urothelial Carcinoma AJCC v6 and v7", "stage 0is bladder urothelial carcinoma aJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder carcinoma in situ", "shortest_name_length": 16}
{"curie": "UMLS:C0861819", "names": ["Small intestine adenocarcinoma metastatic", "Metastatic Small Intestinal Adenocarcinoma", "Small intestine adenocarcinoma metastatic NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small intestine adenocarcinoma metastatic", "shortest_name_length": 41}
{"curie": "UMLS:C3272816", "names": ["Colon Micropapillary Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colon Micropapillary Adenocarcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C0339730", "names": ["Acquired Blindness", "Blindness, Acquired"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Blindness, Acquired", "shortest_name_length": 18}
{"curie": "UMLS:C0035238", "names": ["anomaly; respiratory system", "respiratory system; anomaly", "RESPIRATORY TRACT MALFORMATION", "Respiratory congenital anomaly", "Respiratory tract malformation", "Congenital anomaly;respiratory", "Respiratory System Abnormality", "Congenital anomaly respiratory", "RESPIRATORY CONGENITAL ANOMALY", "Abnormality, Respiratory System", "System Abnormality, Respiratory", "Respiratory System Abnormalities", "Anomaly of respiratory system NOS", "System Abnormalities, Respiratory", "Abnormalities, Respiratory System", "Respiratory tract malformation NOS", "Congenital anomal respiratory system", "ANOMALY CONGENITAL RESPIRATORY (NOS)", "Congenital Respiratory System Disorder", "Respiratory system congenital anomalies", "Congenital Anomaly of Respiratory System", "congenital anomaly of respiratory system", "Congenital respiratory tract malformation", "Unspecified anomaly of respiratory system", "Congenital anomalies of respiratory system", "Anomalies of respiratory system, congenital", "Congenital anomaly of respiratory system NOS", "congenital anomaly of the respiratory system", "Congenital abnormality of respiratory system", "Congenital anomaly of the respiratory system", "Congenital respiratory tract malformation NOS", "Congenital anomaly of respiratory system, NOS", "CONGENITAL ANOMALIES OF THE RESPIRATORY SYSTEM", "Congenital respiratory tract malformation, NOS", "Congenital Abnormality of the Respiratory System", "Congenital malformation of the respiratory system", "Congenital malformations of the respiratory system", "Unspecified congenital anomaly of respiratory system", "congenital anomaly of respiratory system (diagnosis)", "Congenital malformation of respiratory system, unspecified", "Congenital malformations of the respiratory system (Q30-Q34)", "Congenital malformation of the respiratory system (disorder)", "CONGENITAL ANOMALIES OF THE RESPIRATORY SYSTEM: GENERAL TERMS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital abnormality of respiratory system", "shortest_name_length": 27}
{"curie": "UMLS:C0748214", "names": ["Pyriform Fossa Epidermoid Carcinoma", "PYRIFORM SINUS CANCER SQUAMOUS CELL", "Pyriform Sinus Epidermoid Carcinoma", "Epidermoid Carcinoma of Pyriform Sinus", "Pyriform Fossa Squamous Cell Carcinoma", "Epidermoid Carcinoma of Pyriform Fossa", "Pyriform Sinus Squamous Cell Carcinoma", "Squamous Cell Carcinoma of Pyriform Sinus", "Squamous Cell Carcinoma of Pyriform Fossa", "Squamous cell carcinoma of piriform sinus", "Epidermoid Carcinoma of the Pyriform Fossa", "Epidermoid Carcinoma of the Pyriform Sinus", "Squamous Cell Carcinoma of the Pyriform Fossa", "Squamous Cell Carcinoma of the Pyriform Sinus", "Squamous cell carcinoma of piriform sinus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Squamous cell carcinoma of piriform sinus", "shortest_name_length": 35}
{"curie": "MONDO:0008663", "names": ["SVD", "Snowflake retinal degeneration", "SNOWFLAKE VITREORETINAL DEGENERATION", "snowflake vitreoretinal degeneration", "Snowflake vitreoretinal degeneration", "Vitreoretinal degeneration, Snowflake type", "VITREORETINAL DEGENERATION, SNOWFLAKE TYPE", "vitreoretinal degeneration, snowflake type", "snowflake degeneration in hereditary vitreoretinal degeneration", "Snowflake degeneration in hereditary vitreoretinal degeneration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "snowflake vitreoretinal degeneration", "shortest_name_length": 3}
{"curie": "MONDO:0017084", "names": ["leptomyelolipoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leptomyelolipoma", "shortest_name_length": 16}
{"curie": "MONDO:0020429", "names": ["Divided right atrium", "divided right atrium", "Cor triatriatum dexter", "cor triatriatum dexter", "Cor triatriatum dextrum", "cor triatriatum dextrum", "Divided right atrium (disorder)", "cor triatriatum dexter (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cor triatriatum dexter", "shortest_name_length": 20}
{"curie": "MONDO:0004064", "names": ["Iris melanoma", "iris melanoma", "melanoma iris", "Iris Melanoma", "iris; melanoma", "melanoma, iris", "melanoma; iris", "iris melanomas", "melanoma of iris", "Melanoma of Iris", "melanoma of the iris", "Melanoma of the Iris", "melanoma of the Iris", "Iris Malignant Melanoma", "anterior uveal melanoma", "iris malignant melanoma", "iris melanoma (disease)", "malignant iris melanoma", "uveal melanoma, anterior", "melanoma, anterior uveal", "iris intraocular melanoma", "melanoma, uveal, anterior", "malignant melanoma of iris", "intraocular melanoma, iris", "Malignant Melanoma of Iris", "melanoma (disease) of iris", "Malignant melanoma of iris", "melanoma, intraocular, iris", "malignant melanoma of the iris", "Malignant Melanoma of the Iris", "melanoma of iris (physical finding)", "Malignant melanoma of iris (disorder)", "malignant melanoma of iris (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "iris melanoma", "shortest_name_length": 13}
{"curie": "MONDO:0001849", "names": ["Chronic orbital inflammation", "chronic orbital inflammation", "Chronic inflammation of orbit", "chronic inflammation of orbit", "Chronic inflammation of orbit, NOS", "Chronic inflammatory disorders of orbit", "Chronic inflammation of orbit (disorder)", "chronic inflammation of orbit (diagnosis)", "Chronic inflammation of orbit, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic orbital inflammation", "shortest_name_length": 28}
{"curie": "MONDO:0016549", "names": ["primary megaureter, adult-onset form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary megaureter, adult-onset form", "shortest_name_length": 36}
{"curie": "UMLS:C5574736", "names": ["BOS", "Obstructive CLAD", "Obstructive CLADs", "CLAD, Obstructive", "Chronic Graft-Versus-Host Disease", "Bronchiolitis obliterans syndrome", "Chronic Graft Versus Host Disease", "Bronchiolitis Obliterans Syndrome", "Graft-Versus-Host Disease, Chronic", "Bronchiolitis Obliterans Syndromes", "Chronic Graft-Versus-Host Diseases", "Syndrome, Bronchiolitis Obliterans", "Disease, Chronic Graft-Versus-Host", "Graft-Versus-Host Diseases, Chronic", "BOS Bronchiolitis Obliterans Syndrome", "Obstructive Chronic Lung Allograft Dysfunction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bronchiolitis Obliterans Syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0014647", "names": ["CDG1Z", "DEE50", "EIEE50", "CDG-Iz", "CAD-CDG", "CDG1Z, FORMERLY", "CDG syndrome type Iz", "early infantile epileptic encephalopathy 50", "congenital disorder of glycosylation type 1z", "Congenital disorder of glycosylation type 1z", "developmental and epileptic encephalopathy 50", "epileptic encephalopathy, early infantile, 50", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 50", "congenital disorder of glycosylation, type Iz", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 50", "developmental and epileptic encephalopathy, 50", "carbohydrate deficient glycoprotein syndrome type Iz", "Carbohydrate deficient glycoprotein syndrome type Iz", "congenital disorder of glycosylation, type Iz, formerly", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iz, FORMERLY", "Carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase congenital disorder of glycosylation", "CAD-CDG - carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase congenital disorder of glycosylation", "Carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase congenital disorder of glycosylation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 50", "shortest_name_length": 5}
{"curie": "MONDO:0020349", "names": ["AMAN", "acute pure motor GBS", "Acute pure motor GBS", "Acute Motor Axonal Neuropathy", "Acute motor axonal neuropathy", "acute motor axonal neuropathy", "acute pure motor Guillain-Barré syndrome", "Acute pure motor Guillain-Barré syndrome", "acute pure motor Guillain-Barre syndrome", "Acute motor axonal neuropathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute motor axonal neuropathy", "shortest_name_length": 4}
{"curie": "UMLS:C4329674", "names": ["Stage II HPV-Mediated (p16-Positive) Oropharyngeal Throat Cancer", "Clinical Stage II HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage II HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8", "shortest_name_length": 64}
{"curie": "UMLS:C4526593", "names": ["Stage IVB Thymus Epithelial Neoplasm", "Stage IVB Thymic Epithelial Neoplasm AJCC v8", "Stage IVB Thymus Epithelial Neoplasm AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Thymic Epithelial Neoplasm AJCC v8", "shortest_name_length": 36}
{"curie": "MONDO:0018860", "names": ["Basel-Vanagaite-Sirota syndrome", "microlissencephaly-micromelia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microlissencephaly-micromelia syndrome", "shortest_name_length": 31}
{"curie": "MONDO:0018114", "names": ["isolated brachycephaly", "non-syndromic bicoronal synostosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated brachycephaly", "shortest_name_length": 22}
{"curie": "UMLS:C4683231", "names": ["Retinoblastoma by AJCC v8 Clinical Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retinoblastoma by AJCC v8 Clinical Stage", "shortest_name_length": 40}
{"curie": "MONDO:0037792", "names": ["Disorder;carbohydrate metabol", "carbohydrate metabolism disease", "metabolic disorder; carbohydrate", "Carbohydrate metabolism disorder", "carbohydrate; metabolic disorder", "carbohydrate metabolism disorder", "Carbohydrate Metabolism Disorder", "carbohydrate disorders metabolism", "Carbohydrate Metabolism Disorders", "disorder; carbohydrate metabolism", "Disease of carbohydrate metabolism", "DISORDER OF CARBOHYDRATE METABOLISM", "disorder of carbohydrate metabolism", "Disorder of carbohydrate metabolism", "Diseases of Carbohydrate Metabolism", "disorders of carbohydrate metabolism", "DISORDERS OF CARBOHYDRATE METABOLISM", "Carbohydrates--Metabolism--Disorders", "carbohydrate metabolic process disease", "Disorder of carbohydrate metabolism, NOS", "disorder of carbohydrate metabolic process", "carbohydrate metabolism disorder (diagnosis)", "Disorder of carbohydrate metabolism (disorder)", "Disorder of carbohydrate metabolism, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carbohydrate metabolism disease", "shortest_name_length": 29}
{"curie": "MONDO:0042972", "names": ["MENINGOCOCCEMIA", "Meningococcemia", "meningococcemia", "Meningococcaemia", "meningococcaemia", "meningococcal sepsis", "Sepsis meningococcal", "Meningococcal sepsis", "meningococcal; sepsis", "sepsis; meningococcal", "Septicemia meningococcal", "Meningococcal septicemia", "meningococcal septicemia", "Septicaemia meningococcal", "Meningococcal septicaemia", "meningococcal septicaemia", "Meningococcemia (finding)", "Meningococcemia, unspecified", "Meningococcaemia, unspecified", "meningococcal septicemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "meningococcemia", "shortest_name_length": 15}
{"curie": "MONDO:0009619", "names": ["MIMIS", "Microcephaly-micromelia syndrome", "microcephaly-micromelia syndrome", "Microcephaly-Micromelia Syndrome", "MICROCEPHALY-MICROMELIA SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly-micromelia syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C4744716", "names": ["Locally Advanced Unresectable Prostate Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Unresectable Prostate Carcinoma", "shortest_name_length": 48}
{"curie": "UMLS:C0302148", "names": ["clot", "Clot", "Clots", "clots", "Thrombi", "thrombus", "THROMBUS", "Thrombus", "BLOOD CLOT", "blood clot", "Blood Clot", "Blood clot", "Thrombosis", "CLOT BLOOD", "Clot blood", "blood clots", "Blood Clots", "Blood coagulum", "blood clotting", "Blood clot, NOS", "blooding clotting", "Blood coagulum, NOS", "Thrombosis/Thrombus", "Blood clot (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Blood Clot", "shortest_name_length": 4}
{"curie": "UMLS:C1142175", "names": ["Shunt thrombosis", "Shunt Thrombosis", "Vascular Shunt Thrombosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Shunt thrombosis", "shortest_name_length": 16}
{"curie": "MONDO:0025089", "names": ["IBR", "Rednose", "infectious bovine rhinotracheitis", "Infectious Bovine Rhinotracheitis", "Infectious bovine rhinotracheitis", "Rhinotracheitis, Infectious Bovine", "Rhinotracheitis, infectious bovine", "bovine Rhinotracheitis, infectious", "Bovine Rhinotracheitis, Infectious", "Infectious Bovine Rhinotracheitides", "infectious bovine Rhinotracheitides", "bovine Rhinotracheitides, infectious", "Bovine Rhinotracheitides, Infectious", "Rhinotracheitides, infectious bovine", "Rhinotracheitides, Infectious Bovine", "Infectious bovine rhinotracheitis (disorder)", "respiratory tract infection of cattle caused by bovine herpesvirus 1 (BHV-1)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infectious bovine rhinotracheitis", "shortest_name_length": 3}
{"curie": "MONDO:0017676", "names": ["marginal papular palmoplantar keratoderma", "marginal papular palmoplantar hyperkeratosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "marginal papular palmoplantar keratoderma", "shortest_name_length": 41}
{"curie": "UMLS:C4528209", "names": ["Nodal PTCL with TFH Phenotype", "Nodal PTCL with T Follicular Helper Phenotype", "Nodal Peripheral T-Cell Lymphoma with TFH Phenotype", "Nodal peripheral T-cell lymphoma with T follicular helper phenotype", "Nodal Peripheral T-Cell Lymphoma with T Follicular Helper Phenotype", "Nodal peripheral T-cell lymphoma with TFH (T follicular helper) phenotype", "Nodal peripheral T-cell lymphoma with T follicular helper phenotype (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nodal peripheral T-cell lymphoma with T follicular helper phenotype", "shortest_name_length": 29}
{"curie": "UMLS:C0729535", "names": ["viral ear infection", "Ear infection viral", "Viral ear infection", "ear viral infection", "ear infection viral", "ears infection viral", "ear infections viral", "Ear infection viral NOS", "Viral ear infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Viral ear infection", "shortest_name_length": 19}
{"curie": "MONDO:0017409", "names": ["CMV CONGENITAL", "cmv congenital", "congenital cmv", "Antenatal CMV infection", "CMV antenatal infection", "antenatal CMV infection", "Congenital CMV Infection", "congenital cmv infection", "Congenital CMV infection", "CMV Infection, Congenital", "Infection, Congenital CMV", "Congenital CMV Infections", "cytomegalovirus congenital", "congenital cytomegalovirus", "Fetal cytomegalovirus syndrome", "fetal cytomegalovirus syndrome", "Foetal cytomegalovirus syndrome", "Neonatal cytomegaloviral disease", "congenital; cytomegaloviral disease", "Antenatal cytomegalovirus infection", "cytomegaloviral disease; congenital", "antenatal cytomegalovirus infection", "congenital Cytomegaloviral infection", "Congenital Cytomegaloviral Infection", "Congenital cytomegalovirus infection", "Cytomegalovirus infection congenital", "congenital cytomegalovirus infection", "Congenital Cytomegalovirus Infection", "Cytomegalovirus congenital infection", "Infection, Congenital Cytomegalovirus", "Congenital Cytomegalovirus Infections", "Cytomegalovirus Infection, Congenital", "infection; congenital, cytomegaloviral", "congenital; infection, cytomegaloviral", "Fetal cytomegalovirus syndrome (disorder)", "Congenital cytomegalovirus infection (disorder)", "congenital cytomegalovirus infection (diagnosis)", "Mother-to-child transmission of cytomegalovirus syndrome", "mother-to-child transmission of cytomegalovirus syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fetal cytomegalovirus syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0014430", "names": ["MRT45", "mental retardation, autosomal recessive 45", "intellectual disability, autosomal recessive 45", "mental retardation, autosomal recessive type 45", "intellectual disability, autosomal recessive type 45", "autosomal recessive intellectual developmental disorder 45", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 45", "FBXO31 autosomal recessive non-syndromic intellectual disability", "autosomal recessive non-syndromic intellectual disability caused by mutation in FBXO31"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 45", "shortest_name_length": 5}
{"curie": "MONDO:0032868", "names": ["LSKB", "LESSEL-KUBISCH SYNDROME", "lessel-kubisch syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lessel-kubisch syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0033541", "names": ["IMD69", "immunodeficiency 69", "IMMUNODEFICIENCY 69", "immunodeficiency 69, mycobacteriosis", "Ifng Deficiency, Autosomal Recessive", "IFNG DEFICIENCY, AUTOSOMAL RECESSIVE", "Immunodeficiency 69, Mycobacteriosis, Autosomal Recessive", "IMMUNODEFICIENCY 69, MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 69", "shortest_name_length": 5}
{"curie": "UMLS:C5420221", "names": ["Oral Multifocal Epithelial Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral Multifocal Epithelial Hyperplasia", "shortest_name_length": 38}
{"curie": "MONDO:0004093", "names": ["esophageal basaloid cancer", "esophageal basaloid carcinoma", "Esophageal Basaloid Carcinoma", "Basaloid Squamous Carcinoma of Esophagus", "Basaloid squamous carcinoma of esophagus", "basaloid squamous carcinoma of esophagus", "esophageal basaloid squamous cell carcinoma", "Esophageal Basaloid Squamous Cell Carcinoma", "Basaloid Squamous Carcinoma of the Esophagus", "basaloid squamous carcinoma of the esophagus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophageal basaloid carcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0019924", "names": ["UPD(20)pat", "paternal UPD20", "Paternal UPD(20)", "paternal UPD(20)", "paternal uniparental disomy of chromosome 20", "Paternal uniparental disomy of chromosome 20", "paternal uniparental disomy of chromosome type 20", "Paternal UPD20 (uniparental disomy of chromosome 20)", "Paternal uniparental disomy of chromosome 20 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paternal uniparental disomy of chromosome 20", "shortest_name_length": 10}
{"curie": "UMLS:C4329261", "names": ["Acquired Ovarian Failure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired Ovarian Failure", "shortest_name_length": 24}
{"curie": "UMLS:C4521820", "names": ["II", "Stage II Hilar Cholangiocarcinoma", "Stage II Hilar Cholangiocarcinoma AJCC v8", "Stage II Perihilar Cholangiocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Hilar Cholangiocarcinoma AJCC v8", "shortest_name_length": 2}
{"curie": "UMLS:C0334433", "names": ["Junction Nevus", "Junction nevus", "junction nevus", "Junction naevus", "Junctional nevus", "Junctional Nevus", "junctional nevus", "Junctional naevus", "junctional naevus", "Naevus;junctional", "Intraepidermal nevus", "Intraepidermal Nevus", "Junctional nevus NOS", "Junctional naevus NOS", "Junctional Skin Nevus", "Junctional nevus, NOS", "Intraepidermal naevus", "Junctional naevus, NOS", "Junctional Melanocytoma", "Junctional melanocytoma", "Junctional Nevus of Skin", "Junctional melanocytic nevus", "junctional melanocytic nevus", "Intraepidermal Nevus of Skin", "Junctional Nevus of the Skin", "Junctional Melanocytic Nevus", "Junctional melanocytic naevus", "Intra-epidermal nevus of skin", "Intra-epidermal naevus of skin", "Intraepidermal Nevus of the Skin", "Junctional melanocytic nevus of skin", "Junctional melanocytic naevus of skin", "Junctional nevus (morphologic abnormality)", "Junctional melanocytic nevus of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Junctional melanocytic nevus of skin", "shortest_name_length": 14}
{"curie": "MONDO:0009768", "names": ["ODOD recessive", "ODOD, autosomal recessive", "ODOD, AUTOSOMAL RECESSIVE", "ODDD, AUTOSOMAL RECESSIVE", "ODDD, autosomal recessive", "oculodentoosseous dysplasia recessive", "autosomal recessive oculodentodigital dysplasia", "OCULODENTOOSSEOUS DYSPLASIA, AUTOSOMAL RECESSIVE", "oculodentodigital dysplasia, autosomal recessive", "Oculodentoosseous Dysplasia, Autosomal Recessive", "Oculodentodigital Dysplasia, Autosomal Recessive", "oculodentoosseous dysplasia, autosomal recessive", "OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculodentodigital dysplasia, autosomal recessive", "shortest_name_length": 14}
{"curie": "MONDO:0021251", "names": ["Endometrium Tumor", "endometrial tumor", "endometrium tumor", "Endometrial Tumor", "Endometrium Neoplasm", "endometrial neoplasm", "Tumor of Endometrium", "endometrium neoplasm", "Endometrial neoplasm", "Neoplasm endometrium", "tumor of endometrium", "Endometrial Neoplasm", "NEOPLASM ENDOMETRIUM", "ENDOMETRIAL NEOPLASIA", "Neoplasm, Endometrial", "Endometrial neoplasia", "Endometrial Neoplasms", "endometrial neoplasms", "Neoplasms, Endometrial", "Neoplasm of Endometrium", "Neoplasm of endometrium", "neoplasm of endometrium", "tumor of the endometrium", "Tumor of the Endometrium", "Endometrial neoplasm NOS", "Neoplasm of the Endometrium", "neoplasm of the endometrium", "endometrium neoplasm (disease)", "Neoplasm of endometrium (disorder)", "neoplasm of endometrium (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometrium neoplasm", "shortest_name_length": 17}
{"curie": "UMLS:C4055185", "names": ["Continent Epispadias"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Continent Epispadias", "shortest_name_length": 20}
{"curie": "MONDO:0016044", "names": ["FLP", "Oral cleft", "Oral clefting", "Orofacial cleft", "cleft lip palate", "cleft lip/palate", "Cleft;palate/lip", "palate cleft lip", "Cleft lip/palate", "cleft palate lip", "lip cleft palate", "Cleft of the mouth", "cheilopalatoschisis", "Cheilopalatoschisis", "cleft lip and palate", "Cleft lip and palate", "Lip and palate cleft", "Palate and lip cleft", "PALATE AND LIP CLEFT", "CLEFT LIP AND PALATE", "LIP AND PALATE CLEFT", "Cleft palate and lip", "Cleft Lip and Palate", "with cleft lip palate", "Cleft lip, cleft palate", "Cleft palate and cleft lip", "Cleft lip and cleft palate", "cleft palate with cleft lip", "Cleft palate with cleft lip", "alveolar cleft lip and palate", "cleft; lip, with cleft palate", "Alveolar cleft lip and palate", "cleft; palate, with cleft lip", "Cleft palate with cleft lip NOS", "Cleft palate with cleft lip, NOS", "Cleft lip-alveolus-palate syndrome", "cleft lip-alveolus-palate syndrome", "Cleft lip and cleft palate (Q35-Q37)", "Cleft lip and cleft palate disorders", "Cleft palate with cleft lip (disorder)", "cleft palate with cleft lip (diagnosis)", "Cleft palate with cleft lip, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleft lip/palate", "shortest_name_length": 3}
{"curie": "UMLS:C1167717", "names": ["Hepatic cancer stage I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatic cancer stage I", "shortest_name_length": 22}
{"curie": "MONDO:0005989", "names": ["Toxoplasmosis", "toxoplasmosis", "TOXOPLASMOSIS", "toxoplasmoses", "Toxoplasmosis NOS", "Toxoplasmosis (disorder)", "toxoplasmosis (diagnosis)", "disseminated toxoplasmosis", "Toxoplasmosis, unspecified", "Toxoplasma gondii infection", "Toxoplasma gondii Infection", "infection; Toxoplasma gondii", "Toxoplasma gondii; infection", "Infection, Toxoplasma gondii", "Infection by Toxoplasma gondii", "infection due to Toxoplasma gondii", "disease (or disorder); toxoplasmosis", "Toxoplasma gondii infectious disease", "Toxoplasma gondii disease or disorder", "Toxoplasma gondii caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "toxoplasmosis", "shortest_name_length": 13}
{"curie": "MONDO:0011201", "names": ["ETM2", "essential tremor 2", "hereditary essential tremor 2", "tremor hereditary essential, 2", "Tremor hereditary essential, 2", "essential tremor, hereditary, 2", "Tremor, Hereditary Essential, 2", "TREMOR, HEREDITARY ESSENTIAL, 2", "tremor, hereditary essential, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tremor, hereditary essential, 2", "shortest_name_length": 4}
{"curie": "UMLS:C5552969", "names": ["Reactogenicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reactogenicity", "shortest_name_length": 14}
{"curie": "MONDO:0007831", "names": ["INSECT STINGS, HYPERSENSITIVITY TO", "insect Stings, hypersensitivity to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "insect Stings, hypersensitivity to", "shortest_name_length": 34}
{"curie": "MONDO:0020724", "names": ["CCM", "CAM", "CCM1", "Familial Cavernous Angioma", "Brain Cavernous Hemangioma", "Angioma, Familial Cavernous", "Cavernous Angioma, Familial", "Brain Cavernous Hemangiomas", "Familial Cavernous Angiomas", "cavernous angioma, familial", "CAVERNOUS ANGIOMA, FAMILIAL", "Angiomas, Familial Cavernous", "Cavernous Angiomas, Familial", "cavernous hemangioma of brain", "Cavernous Hemangioma of Brain", "Cavernous hemangioma of brain", "Cavernous haemangioma of brain", "Cerebral cavernous malformation", "Familial Cavernous Malformation", "Cerebral Cavernous Malformation", "Cerebral Capillary Malformation", "CEREBRAL CAVERNOUS MALFORMATIONS", "Capillary Malformation, Cerebral", "Malformation, Cerebral Capillary", "Cavernous Malformation, Cerebral", "Malformation, Familial Cavernous", "cerebral capillary malformations", "Malformation, Cerebral Cavernous", "cerebral cavernous malformations", "Cavernous Malformation, Familial", "Cerebral Cavernous Malformations", "Cerebral Capillary Malformations", "Cerebral cavernous malformations", "Familial Cavernous Malformations", "CEREBRAL CAPILLARY MALFORMATIONS", "Capillary Malformations, Cerebral", "Cavernous Malformations, Familial", "Cavernous Malformations, Cerebral", "Malformations, Cerebral Cavernous", "cerebral cavernous malformation 1", "Malformations, Cerebral Capillary", "Malformations, Familial Cavernous", "Cerebral Cavernous Malformations 1", "cerebral cavernous malformations-1", "CEREBRAL CAVERNOUS MALFORMATIONS 1", "cerebral cavernous malformations 1", "Cavernous Angiomatous Malformation", "Malformation, Cavernous Angiomatous", "Cavernous Angiomatous Malformations", "CAVERNOUS ANGIOMATOUS MALFORMATIONS", "cavernous angiomatous malformations", "Angiomatous Malformation, Cavernous", "Malformations, Cavernous Angiomatous", "Angiomatous Malformations, Cavernous", "Cavernous hemangioma of brain (disorder)", "CAVERNOUS MALFORMATIONS OF CNS AND RETINA", "Cavernous Malformations of CNS and Retina", "cavernous hemangioma of brain (diagnosis)", "cavernous malformations of CNS and retina", "familial cerebral cavernous malformation 1", "HYPERKERATOTIC CUTANEOUS CAPILLARY-VENOUS MALFORMATIONS ASSOCIATED WITH CEREBRAL CAPILLARY MALFORMATIONS", "hyperkeratotic cutaneous capillary-Venous malformations associated with cerebral capillary malformations", "Hyperkeratotic Cutaneous Capillary-Venous Malformations Associated With Cerebral Capillary Malformations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral cavernous malformation 1", "shortest_name_length": 3}
{"curie": "MONDO:0013659", "names": ["MICCAP", "MIC-CM syndrome", "MIC-CAP syndrome", "MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME", "Microcephaly-capillary malformation syndrome", "microcephaly-capillary malformation syndrome", "microcephaly-cutaneous capillary malformation syndrome", "Microcephaly-cutaneous capillary malformation syndrome", "Microcephaly-capillary malformation syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly-capillary malformation syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C1096444", "names": ["Altered visual depth perception"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Altered visual depth perception", "shortest_name_length": 31}
{"curie": "MONDO:0006654", "names": ["Melanedema", "Black Lung", "black lung", "Lung, Black", "melanoedema", "anthracosis", "Anthracosis", "lung; black", "Melanoedema", "Black Lungs", "Anthracoses", "black lungs", "ANTHRACOSIS", "black; lung", "collier lung", "Lungs, Black", "Miners' lung", "miner's; lung", "Colliers' lung", "Miners' asthma", "Miner's asthma", "Lung melanosis", "Pneumomelanosis", "Coal Miner Lung", "coal lung miners", "Coal Miners Lung", "coalworker's lung", "Coal miners' lung", "Coalworker's lung", "Coal Miner's Lung", "Coal workers' lung", "coal workers' lung", "Black Lung Disease", "Miner's Lung, Coal", "Coal Miner's Lungs", "Black lung disease", "Coal worker's lung", "black lung disease", "Coal pneumoconiosis", "Black Lung Diseases", "coal lungs worker's", "Miner's Lungs, Coal", "pneumoconiosis coal", "PULMONARY ANTHRACOSIS", "Colliers' anthracosis", "pneumoconiosis; miner's", "miner's; pneumoconiosis", "coal dust pneumoconiosis", "Coalworker Pneumoconiosis", "coalworker; pneumoconiosis", "pneumoconiosis; coalworker", "coal miners pneumoconiosis", "Coal Worker Pneumoconiosis", "Coalworkers Pneumoconiosis", "Coalworker's pneumoconiosis", "Pneumoconiosis, Coal Worker", "coal miners' pneumoconiosis", "Coal miner's pneumoconiosis", "coalworker's pneumoconiosis", "Coal Workers Pneumoconiosis", "Coalworker's Pneumoconioses", "Coal Miner's Pneumoconiosis", "coal miner's pneumoconiosis", "Coal miners' pneumoconiosis", "Coalworker's Pneumoconiosis", "coal pneumoconiosis workers", "Pneumoconioses, Coalworker's", "coal workers' pneumoconiosis", "Coal Worker's Pneumoconiosis", "Pneumoconiosis, Coalworker's", "Coal workers' pneumoconiosis", "Coal Worker's Pneumoconioses", "coal pneumoconiosis workers'", "Pneumoconiosis, Coal Workers", "pneumoconiosis from coal dust", "Pneumoconioses, Coal Worker's", "Pneumoconiosis, Coal Worker's", "lung; fibrosis, with anthracosis", "CWP - Coalworkers pneumoconiosis", "fibrosis; lung, with anthracosis", "fibrosis; lung, with anthracosilicosis", "lung; fibrosis, with anthracosilicosis", "Coal workers' pneumoconiosis (disorder)", "coal workers' pneumoconiosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anthracosis", "shortest_name_length": 10}
{"curie": "UMLS:C4329676", "names": ["Stage IV HPV-Mediated (p16-Positive) Oropharyngeal Throat Cancer", "Clinical Stage IV HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage IV HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8", "shortest_name_length": 64}
{"curie": "MONDO:0001631", "names": ["PICA syndrome", "Vertebral artery syndrome", "vertebral artery syndrome", "Vertebral Artery Syndrome", "Vertebral Artery Ischemia", "syndrome; vertebral artery", "Ischemia, Vertebral Artery", "Artery Ischemia, Vertebral", "Vertebral Artery Ischemias", "Ischemias, Vertebral Artery", "Artery Ischemias, Vertebral", "a.vertebralis; insufficiency", "vertebral artery insufficiency", "Vertebral Artery Insufficiency", "Artery Insufficiency, Vertebral", "Insufficiency, Vertebral Artery", "insufficiency; vertebral artery", "Vertebral Artery Insufficiencies", "Insufficiencies, Vertebral Artery", "Artery Insufficiencies, Vertebral", "Vertebral artery syndrome (disorder)", "vertebral artery compression syndrome", "Vertebral artery compression syndrome", "Vertebral artery compression syndromes", "vertebral artery compression syndrome (diagnosis)", "Vertebral artery compression syndromes, site unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vertebral artery insufficiency", "shortest_name_length": 13}
{"curie": "UMLS:C0019054", "names": ["Hemolysis", "HEMOLYSIS", "hemolysis", "HAEMOLYSIS", "Haemolysis", "Haemolyses", "Hemolysis NOS", "Haemolysis NOS", "Hemolysis (disorder)", "hemolysis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemolysis (disorder)", "shortest_name_length": 9}
{"curie": "UMLS:C3889290", "names": ["GRADE 3", "West Haven Hepatic Encephalopathy Grade 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "West Haven Hepatic Encephalopathy Grade 3", "shortest_name_length": 7}
{"curie": "MONDO:0008454", "names": ["Intradural spinal arachnoid cyst", "spinal intradural arachnoid cysts", "Spinal intradural arachnoid cysts", "SPINAL INTRADURAL ARACHNOID CYSTS", "arachnoid cysts, spinal intradural", "Arachnoid cysts, spinal intradural", "Intradural spinal arachnoid cyst (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal intradural arachnoid cysts", "shortest_name_length": 32}
{"curie": "UMLS:C5555195", "names": ["Platinum-Refractory Ovarian Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Platinum-Refractory Ovarian Carcinoma", "shortest_name_length": 37}
{"curie": "UMLS:C5235856", "names": ["Metastatic Digestive System Mixed Adenoneuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Digestive System Mixed Adenoneuroendocrine Carcinoma", "shortest_name_length": 63}
{"curie": "MONDO:0013143", "names": ["THPH11", "thrombophilia due to HRG deficiency", "thrombophilia 11 due to HRG deficiency", "hereditary thrombophilia due to congenital HRG deficiency", "thrombophilia due to elevated histidine-rich glycoprotein", "Thrombophilia Due To Elevated Histidine-Rich Glycoprotein", "THROMBOPHILIA DUE TO ELEVATED HISTIDINE-RICH GLYCOPROTEIN", "Thrombophilia Due To Histidine-Rich Glycoprotein Deficiency", "THROMBOPHILIA DUE TO HISTIDINE-RICH GLYCOPROTEIN DEFICIENCY", "thrombophilia due to histidine-rich glycoprotein deficiency", "hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency", "shortest_name_length": 6}
{"curie": "MONDO:0011446", "names": ["MYOCLONIC EPILEPSY, CONGENITAL DEAFNESS, MACULAR DYSTROPHY, AND PSYCHIATRIC DISORDERS", "Myoclonic Epilepsy, Congenital Deafness, Macular Dystrophy, and Psychiatric Disorders", "myoclonic epilepsy, congenital deafness, macular dystrophy, and psychiatric disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myoclonic epilepsy, congenital deafness, macular dystrophy, and psychiatric disorders", "shortest_name_length": 85}
{"curie": "MONDO:0006481", "names": ["ureter cancer", "Ureter Cancer", "Ureter Carcinoma", "Carcinoma;ureter", "ureter carcinoma", "URETER, CARCINOMA", "Ureteral Carcinoma", "ureteral carcinoma", "Carcinoma of Ureter", "Carcinoma of ureter", "carcinoma of ureter", "carcinoma of the ureter", "Carcinoma of the Ureter", "URETERAL CANCER, CARCINOMA", "carcinoma of ureter (diagnosis)", "Malignant epithelial neoplasm of ureter", "Malignant epithelial neoplasm of ureter (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ureter carcinoma", "shortest_name_length": 13}
{"curie": "MONDO:0001336", "names": ["hyperlipemia", "hyperlipidaemia", "familial hyperlipemia", "familial hyperlipidemia", "familial hyperlipoproteinemia", "hereditary hyperlipidemia (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial hyperlipidemia", "shortest_name_length": 12}
{"curie": "UMLS:C4727065", "names": ["Refractory Hepatosplenic T-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Hepatosplenic T-Cell Lymphoma", "shortest_name_length": 40}
{"curie": "MONDO:0005725", "names": ["cyclosporosis", "Cyclosporosis", "cyclosporiasis", "Cyclosporiases", "Cyclosporiasis", "Cyclospora infection", "Cyclosporiasis (disorder)", "cyclosporiasis (diagnosis)", "Cyclospora infectious disease", "Cyclospora disease or disorder", "Cyclospora caused disease or disorder", "Cyclospora cayetanensis infectious disease", "Cyclospora cayetanensis disease or disorder", "cyclosporiasis caused by cyclospora cayetanensis", "Cyclospora cayetanensis caused disease or disorder", "Intestinal infection caused by cyclospora cayetanensis", "intestinal infection caused by Cyclospora cayetanensis", "infection of intestine caused by Cyclospora cayetanensis", "Infection of intestine caused by cyclospora cayetanensis", "Intestinal infection caused by cyclospora cayetanensis (diagnosis)", "Infection of intestine caused by cyclospora cayetanensis (disorder)", "gastrointestinal infections cyclosporiasis caused by cyclospora cayetanensis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cyclosporiasis", "shortest_name_length": 13}
{"curie": "UMLS:C2938941", "names": ["Infective pulmonary exacerbation of cystic fibrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infective pulmonary exacerbation of cystic fibrosis", "shortest_name_length": 51}
{"curie": "MONDO:0003408", "names": ["Ovarian Primitive Germ Cell Tumor", "ovarian primitive germ cell tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian primitive germ cell tumor", "shortest_name_length": 33}
{"curie": "MONDO:0014174", "names": ["RHPD2", "renal-hepatic-pancreatic dysplasia 2", "RENAL-HEPATIC-PANCREATIC DYSPLASIA 2", "NEK8 renal-hepatic-pancreatic dysplasia", "renal-hepatic-pancreatic dysplasia type 2", "renal-hepatic-pancreatic dysplasia caused by mutation in NEK8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal-hepatic-pancreatic dysplasia 2", "shortest_name_length": 5}
{"curie": "MONDO:0012052", "names": ["CDG1K", "CDGIk", "CDG Ik", "CDG 1K", "CDG-Ik", "ALG1-CDG", "ALG1-CDG (CDG-Ik)", "CDG syndrome type Ik", "mannosyltransferase 1 deficiency", "Mannosyltransferase 1 deficiency", "congenital disorder of glycosylation 1k", "congenital disorder of glycosylation Ik", "ALG1-congenital disorder of glycosylation", "ALG1 congenital disorder of glycosylation", "Congenital disorder of glycosylation type Ik", "congenital disorder of glycosylation type Ik", "Congenital disorder of glycosylation type 1k", "Congenital disorder of glycosylation type 1K", "congenital disorder of glycosylation type 1k", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ik", "Congenital Disorder Of Glycosylation, Type IK", "congenital disorder of glycosylation, type Ik", "carbohydrate deficient glycoprotein syndrome type Ik", "Carbohydrate deficient glycoprotein syndrome type Ik", "Asparagine-linked glycosylation 1 congenital disorder of glycosylation", "ALG1-CDG - asparagine-linked glycosylation 1 congenital disorder of glycosylation", "Asparagine-linked glycosylation 1 congenital disorder of glycosylation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ALG1-congenital disorder of glycosylation", "shortest_name_length": 5}
{"curie": "MONDO:0014078", "names": ["BDPLT15", "platelet-type bleeding disorder 15", "bleeding disorder, platelet-type, 15", "BLEEDING DISORDER, PLATELET-TYPE, 15", "ACTN1 inherited bleeding disorder, platelet-type", "autosomal dominant macrothrombocytopenia ACTN1-related", "macrothrombocytopenia, autosomal dominant, ACTN1-related", "MACROTHROMBOCYTOPENIA, AUTOSOMAL DOMINANT, ACTN1-RELATED", "inherited bleeding disorder, platelet-type caused by mutation in ACTN1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "platelet-type bleeding disorder 15", "shortest_name_length": 7}
{"curie": "MONDO:0000957", "names": ["Lacrimal sac granuloma", "granuloma; lacrimal sac", "lacrimal sac; granuloma", "lacrimal passage granuloma", "Lacrimal passage granuloma", "Granuloma of lacrimal passages", "granuloma of lacrimal passages", "Lacrimal sac granuloma (disorder)", "lacrimal passage granuloma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lacrimal passage granuloma", "shortest_name_length": 22}
{"curie": "MONDO:0016515", "names": ["Kallmann syndrome-heart disease syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kallmann syndrome-heart disease syndrome", "shortest_name_length": 40}
{"curie": "MONDO:0008811", "names": ["XK SYNDROME", "Xk syndrome", "XK syndrome", "Atelencephaly", "atelencephaly", "XK aprosencephaly", "XK-aprosencephaly", "Garcia Lurie syndrome", "GARCIA-LURIE SYNDROME", "Garcia-Lurie syndrome", "APROSENCEPHALY SYNDROME", "aprosencephaly syndrome", "Aprosencephaly syndrome", "Atelencephaly (disorder)", "atelencephaly (diagnosis)", "XK aprosencephaly syndrome", "XK-aprosencephaly syndrome", "Atelencephalic microcephaly", "atelencephalic microcephaly syndrome", "Aprosencephaly-atelencephaly syndrome", "XK aprosencephaly syndrome (disorder)", "aprosencephaly-atelencephaly syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "XK aprosencephaly", "shortest_name_length": 11}
{"curie": "MONDO:0000733", "names": ["Flat cornea", "flat cornea", "cornea plana", "Cornea plana", "plana; cornea", "cornea; plana", "flattened cornea", "Cornea flattened", "cornea flattening", "Cornea plana (disorder)", "Congenital cornea plana"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cornea plana", "shortest_name_length": 11}
{"curie": "UMLS:C1512907", "names": ["Intestinal Metaplasia of Bladder Urothelium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal Metaplasia of Bladder Urothelium", "shortest_name_length": 43}
{"curie": "UMLS:C5419785", "names": ["Rectal Conventional Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rectal Conventional Adenoma", "shortest_name_length": 27}
{"curie": "UMLS:C5237719", "names": ["Oligometastatic Esophageal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oligometastatic Esophageal Adenocarcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0005324", "names": ["hayfever", "HAYFEVER", "Hayfever", "Hay Fever", "Hay fever", "HAY FEVER", "fever hay", "hay fever", "Pollenosis", "pollinosis", "Pollinoses", "pollenosis", "Pollinosis", "Fever, Hay", "pollen allergy", "allergy pollen", "Pollen allergy", "Pollen Allergy", "pollen; allergy", "Allergy, Pollen", "allergy; pollen", "ALLERGY SEASONAL", "seasonal allergy", "allergies pollen", "Seasonal allergy", "Pollen Allergies", "ALLERGY TO POLLEN", "Allergy to pollen", "allergy to pollen", "Allergies, Pollen", "allergy to pollens", "SEASONAL ALLERGIES", "seasonal allergies", "Seasonal Allergies", "allergic to pollens", "Spasmodic rhinorrhea", "spasmodic rhinorrhea", "Spasmodic rhinorrhoea", "hay fever (diagnosis)", "rhinorrhea; spasmodic", "spasmodic; rhinorrhea", "RHINITIS ALLERGIC SEASONAL", "SEASONAL ALLERGIC REACTION", "Seasonal Allergic Rhinitis", "seasonal allergic rhinitis", "Seasonal allergy (finding)", "Seasonal allergic rhinitis", "allergy to pollen (history)", "Allergic Rhinitis, Seasonal", "Allergy to pollen (finding)", "Rhinitis, Seasonal Allergic", "Rhinitis, Allergic, Seasonal", "Seasonal Allergic Rhinitides", "rhinitis; allergic, seasonal", "Rhinitides, Seasonal Allergic", "Allergic Rhinitides, Seasonal", "Allergic rhinitis due to pollen", "allergic rhinitis due to pollen", "spasmodic rhinorrhea (diagnosis)", "Allergic rhinitis due to pollens", "allergic; rhinitis, due to pollen", "rhinitis; allergic, due to pollen", "Allergic rhinitis caused by pollen", "Allergic rhinitis caused by pollens", "Seasonal allergic rhinitis (disorder)", "rhinitis; allergic, seasonal, due to pollen", "allergic; rhinitis, seasonal, due to pollen", "allergic rhinitis due to pollen (diagnosis)", "Allergic rhinitis caused by pollen (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "seasonal allergic rhinitis", "shortest_name_length": 8}
{"curie": "UMLS:C0684830", "names": ["Axillary metastases", "Axillary Metastases", "Axillary Metastasis", "Secondary malignant neoplasm of axilla", "Metastatic malignant neoplasm of axilla", "Metastatic malignant neoplasm to axilla", "Metastatic Malignant Tumor to the Axilla", "Metastatic Malignant Neoplasm to the Axilla", "Secondary malignant neoplasm of axilla, NOS", "Metastatic Malignant Neoplasm in the Axilla", "Metastatic malignant neoplasm to axilla, NOS", "Secondary malignant neoplasm of axilla (diagnosis)", "Metastatic malignant neoplasm to axilla (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to axilla", "shortest_name_length": 19}
{"curie": "MONDO:0011075", "names": ["RP18", "RP 18", "retinitis pigmentosa 18", "Retinitis Pigmentosa 18", "RETINITIS PIGMENTOSA 18", "PRPF3 retinitis pigmentosa", "retinitis pigmentosa type 18", "retinitis pigmentosa caused by mutation in PRPF3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 18", "shortest_name_length": 4}
{"curie": "MONDO:0004148", "names": ["gallbladder papillary carcinoma", "gall bladder papillary carcinoma", "Papillary Carcinoma of Gallbladder", "papillary carcinoma of gallbladder", "Gallbladder papillary adenocarcinoma", "Papillary carcinoma of the gallbladder", "Papillary Carcinoma of the Gallbladder", "papillary carcinoma of the gallbladder", "papillary adenocarcinoma of gallbladder", "papillary carcinoma of gallbladder (diagnosis)", "papillary adenocarcinoma of gallbladder (diagnosis)", "Gallbladder ICPN with an Associated Invasive Carcinoma", "Gallbladder Papillary Neoplasm with an Associated Invasive Cancer", "gallbladder papillary neoplasm with an associated invasive cancer", "intracystic papillary neoplasm with an associated invasive carcinoma", "Intracystic Papillary Neoplasm with an Associated Invasive Carcinoma", "Gallbladder Papillary Neoplasm with an Associated Invasive Carcinoma", "gallbladder papillary neoplasm with an associated invasive carcinoma", "Gallbladder Intracholecystic Papillary Neoplasm with an Associated Invasive Carcinoma", "Gallbladder Intracystic/Intaductal Papillary Neoplasm with an Associated Invasive Carcinoma", "Gallbladder Intracholecystic Papillary (Tubular) Neoplasm with an Associated Invasive Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gallbladder papillary neoplasm with an associated invasive carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0010298", "names": ["LNS", "Lesch-Nyhan", "nyhan syndrome", "NYHAN SYNDROME", "nyhans syndrome", "HPRT DEFICIENCY", "HPRT deficiency", "Hprt1 deficiency", "HPRT1 deficiency", "HPRT1 DEFICIENCY", "HGPRT Deficiency", "HGPRT deficiency", "HG-PRT deficiency", "Deficiency, HGPRT", "HGPRT Deficiencies", "Lesch-Nyhan disease", "Lesch Nyhan Disease", "Lesch Nyhan disease", "lesch nyhan disease", "Deficiencies, HGPRT", "lesch-nyhan disease", "Lesch-Nyhan Disease", "lesch-nyhan syndrome", "Lesch-Nyhan syndrome", "lesch nyhan syndrome", "LESCH NYHAN SYNDROME", "Lesch Nyhan Syndrome", "Lesch Nyhan syndrome", "Lesch-Nyhan Syndrome", "LESCH-NYHAN SYNDROME", "Total HPRT Deficiency", "X-linked hyperuricemia", "Total HGPRT deficiency", "Lesch - Nyhan syndrome", "Deficiency, Total HPRT", "X-Linked Hyperuricemia", "X Linked Hyperuricemia", "HPRT Deficiency, Total", "X-linked hyperuricaemia", "X-Linked Hyperuricemias", "Total HPRT Deficiencies", "Hyperuricemia, X-Linked", "Deficiencies, Total HPRT", "Hyperuricemias, X-Linked", "HPRT deficiency grade IV", "HPRT Deficiencies, Total", "HPRT complete deficiency", "Complete HPRT Deficiency", "HEREDITARY HYPERURICEMIA", "HPRT Deficiency, Complete", "HPRT DEFICIENCY, COMPLETE", "Complete HGPRT deficiency", "HPRT deficiency, complete", "Deficiency, Complete HPRT", "Lesch-Nyhan syndrome (LNS)", "HG-PRT deficiency syndrome", "Complete HPRT Deficiencies", "HPRT Deficiencies, Complete", "Deficiencies, Complete HPRT", "X Linked Primary Hyperuricemia", "X-Linked Primary Hyperuricemia", "primary hyperuricemia syndrome", "X-linked primary hyperuricemia", "Primary Hyperuricemia Syndrome", "X-Linked Primary Hyperuricemias", "Syndrome, Primary Hyperuricemia", "Primary Hyperuricemia Syndromes", "Juvenile Hyperuricemia Syndrome", "Hyperuricemia Syndrome, Primary", "juvenile hyperuricemia syndrome", "Lesch-Nyhan syndrome (disorder)", "Primary Hyperuricemia, X-Linked", "Hyperuricemia, X-Linked Primary", "Syndromes, Primary Hyperuricemia", "Syndrome, Juvenile Hyperuricemia", "Hyperuricemia Syndrome, Juvenile", "Primary Hyperuricemias, X-Linked", "Hyperuricemias, X-Linked Primary", "Lesch-Nyhan syndrome (diagnosis)", "Juvenile Hyperuricemia Syndromes", "Hyperuricemia Syndromes, Primary", "Complete HGPRT Deficiency Disease", "Hyperuricemia Syndromes, Juvenile", "Syndromes, Juvenile Hyperuricemia", "HGPRT Deficiency Disease, Complete", "Deficiency Disease, Complete HGPRT", "Deficiency of IMP pyrophosphorylase", "HPRT deficiency, neurologic variant", "deficiency of IMP pyrophosphorylase", "HPRT DEFICIENCY, NEUROLOGIC VARIANT", "HPRT Deficiency, Neurologic Variant", "X-linked uric aciduria enzyme defect", "Lesch-Nyhan syndrome (HGPRT deficiency)", "Lesch-Nyhan Syndrome, Neurologic Variant", "Lesch-Nyhan syndrome, neurologic variant", "Choreoathetosis Self-Mutilation Syndrome", "Choreoathetosis self-mutilation syndrome", "Lesch-Nyhan syndrome, X-linked recessive", "LESCH-NYHAN SYNDROME, NEUROLOGIC VARIANT", "Choreoathetosis Self Mutilation Syndrome", "Choreoathetosis Self-Mutilation Syndromes", "Syndrome, Choreoathetosis Self-Mutilation", "Self-Mutilation Syndrome, Choreoathetosis", "Syndromes, Choreoathetosis Self-Mutilation", "Self-Mutilation Syndromes, Choreoathetosis", "Guanine Phosphoribosyltransferase Deficiency", "X-linked hyperuricemia (disorder) [ambiguous]", "Phosphoribosyltransferase Deficiency, Guanine", "Guanine Phosphoribosyltransferase Deficiencies", "Phosphoribosyltransferase Deficiencies, Guanine", "Deficiency of Guanine Phosphoribosyltransferase", "Deficiency of guanine phosphoribosyltransferase", "hypoxanthine phosphoribosyltransferse deficiency", "Hypoxanthine Phosphoribosyltransferase Deficiency", "Deficiency, Hypoxanthine Phosphoribosyltransferase", "Phosphoribosyltransferase Deficiency, Hypoxanthine", "Hypoxanthine Phosphoribosyltransferase Deficiencies", "Deficiency of Hypoxanthine Phosphoribosyltransferase", "Deficiencies, Hypoxanthine Phosphoribosyltransferase", "Phosphoribosyltransferase Deficiencies, Hypoxanthine", "Deficiency of hypoxanthine phosphoribosyltransferase", "Choreoathetosis Self-Mutilation Hyperuricemia Syndrome", "Choreoathetosis Self Mutilation Hyperuricemia Syndrome", "hypoxanthine phosphoribosyltransferse (HPRT) deficiency", "HYPERURICEMIA, CHOREOATHETOSIS, SELF-MUTILATION SYNDROME", "Hypoxanthine-guanine phosphoribosyltransferase deficiency", "Hypoxanthine-guanine-phosphoribosyltransferase deficiency", "hypoxanthine guanine phosphoribosyltransferase deficiency", "hypoxanthine-guanine phosphoribosyltransferase deficiency", "Hypoxanthine Guanine Phosphoribosyltransferase Deficiency", "Hypoxanthine-guanine phosphoribosyl transferase deficiency", "Hypoxanthine-Phosphoribosyl-Transferase Deficiency Disease", "Hypoxanthine Phosphoribosyl Transferase Deficiency Disease", "Hypoxanthine-guanine phosphoribosyltransferase 1 deficiency", "Juvenile Gout, Choreoathetosis, Mental Retardation Syndrome", "JUVENILE GOUT, CHOREOATHETOSIS, MENTAL RETARDATION SYNDROME", "Deficiency Disease, Hypoxanthine-Phosphoribosyl-Transferase", "HYPOXANTHINE GUANINE PHOSPHORIBOSYLTRANSFERASE 1 DEFICIENCY", "hypoxanthine guanine phosphoribosyltransferase 1 deficiency", "Hypoxanthine Guanine Phosphoribosyltransferase 1 Deficiency", "Deficiency Disease, Hypoxanthine Phosphoribosyl Transferase", "Hypoxanthine-Phosphoribosyl-Transferase Deficiency Diseases", "deficiency; hypoxanthine(-guanine)-phosphoribosyltransferase", "Deficiency of hypoxanthine-guanine phosphoribosyltransferase", "hypoxanthine(-guanine)-phosphoribosyltransferase; deficiency", "hypoxanthine guanine phospho-ribosyltransferase 1 deficiency", "Deficiency Diseases, Hypoxanthine-Phosphoribosyl-Transferase", "Hypoxanthine-guanine phosphoribosyltransferase deficiency, NOS", "Deficiency of hypoxanthine phosphoribosyltransferase (disorder)", "Total Hypoxanthine-Guanine Phosphoribosyl Transferase Deficiency", "Total hypoxanthine-guanine phosphoribosyl transferase deficiency", "Total Hypoxanthine Guanine Phosphoribosyl Transferase Deficiency", "HPRT - Hypoxanthine-guanine phosphoribosyltransferase deficiency", "hypoxanthine-guanine phosphoribosyltransferase (HGPRT) deficiency", "Complete Hypoxanthine-Guanine Phosphoribosyltransferase Deficiency", "Complete Hypoxanthine Guanine Phosphoribosyltransferase Deficiency", "Hypoxanthine guanine phosphoribosyltransferase complete deficiency", "Complete hypoxanthine-guanine phosphoribosyltransferase deficiency", "Hypoxanthine-guanine-phosphoribosyltransferase deficiency syndrome", "complete hypoxanthine-guanine phosphoribosyltransferase deficiency", "hypoxanthine guanine phosphoribosyltransferase complete deficiency", "hypoxanthine guanine phosphoribosyltransferase deficiency, grade IV", "Hypoxanthine guanine phosphoribosyltransferase deficiency, grade IV", "hypoxanthine-guanine-phosphoribosyltransferase deficiency (& [Lesch - Nyhan syndrome])"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lesch-Nyhan syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0011544", "names": ["PGL3", "PARAGANGLIOMAS 3", "paragangliomas 3", "Paragangliomas 3", "SDHC paraganglioma", "paragangliomas type 3", "glomus tumors, familial, 3", "GLOMUS TUMORS, FAMILIAL, 3", "Glomus Tumors, Familial, 3", "paraganglioma caused by mutation in SDHC", "SDHC-related hereditary paraganglioma-pheochromocytoma syndrome (paragangliomas 3)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paragangliomas 3", "shortest_name_length": 4}
{"curie": "MONDO:0012768", "names": ["HPC11", "PROSTATE CANCER, HEREDITARY, 11", "prostate cancer, hereditary, 11", "Prostate Cancer, Hereditary, 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate cancer, hereditary, 11", "shortest_name_length": 5}
{"curie": "MONDO:0021764", "names": ["acrofacial dysostosis Preis type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acrofacial dysostosis Preis type", "shortest_name_length": 32}
{"curie": "UMLS:C5418961", "names": ["HPV-Related Mucosal Head and Neck Squamous Cell Carcinoma", "HPV-Associated Mucosal Head and Neck Squamous Cell Carcinoma", "Human Papillomavirus-Related Mucosal Head and Neck Squamous Cell Carcinoma", "Human Papillomavirus-Associated Mucosal Head and Neck Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Human Papillomavirus-Related Mucosal Head and Neck Squamous Cell Carcinoma", "shortest_name_length": 57}
{"curie": "MONDO:0004684", "names": ["Plantar fibroma", "Lederhose disease", "Ledderhose Disease", "Ledderhose disease", "plantar fibromatosis", "Ledderhose's Disease", "ledderhose's disease", "fibromatosis plantar", "Plantar Fibromatosis", "Ledderhose's disease", "Plantar fibromatosis", "plantar; fibromatosis", "fibromatosis; plantar", "Fibromatosis, Plantar", "Dupuytren disease of foot", "plantar fascial fibromatosis", "Plantar fascial fibromatosis", "[OBSOLETE] Ledderhose disease", "Dupuytren's contracture of foot", "Plantar fascial fibromatosis (disorder)", "plantar fascial fibromatosis (diagnosis)", "plantar part of pes superficial Fibromatosis", "plantar part of pes superficial fibromatosis", "superficial fibromatosis of plantar part of pes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "plantar fibromatosis", "shortest_name_length": 15}
{"curie": "UMLS:C4763793", "names": ["Recurrent NK-Cell Lymphoma, Unclassifiable"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent NK-Cell Lymphoma, Unclassifiable", "shortest_name_length": 42}
{"curie": "UMLS:C0852624", "names": ["Extranodal marginal zone B-cell lymphoma (MALT type)", "Extranodal marginal zone B-cell lymphoma (MALT type) NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extranodal marginal zone B-cell lymphoma (MALT type)", "shortest_name_length": 52}
{"curie": "MONDO:0012248", "names": ["MDDGC1", "LGMD2K", "LGMDR11", "LGMD type 2K", "LGMD-POMT1 related", "POMT1-related LGMD R11", "limb-girdle muscular dystrophy type 2K", "Limb-girdle muscular dystrophy type 2K", "muscular dystrophy limb-girdle type 2K", "Muscular Dystrophy, Limb-Girdle, Type 2K", "muscular dystrophy, limb-girdle, type 2K", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K", "POMT1-related limb-girdle muscular dystrophy R11", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 11", "limb-girdle muscular dystrophy - intellectual disability", "POMT1 autosomal recessive limb-girdle muscular dystrophy", "Autosomal recessive limb girdle muscular dystrophy type 2K", "autosomal recessive limb-girdle muscular dystrophy type 2K", "Autosomal recessive limb-girdle muscular dystrophy type 2K", "muscular dystrophy-dystroglycanopathy (limb-girdle) type C 1", "muscular dystrophy-dystroglycanopathy (Limb-girdle) type C, 1", "Muscular Dystrophy-Dystroglycanopathy (Limb-Girdle) Type C, 1", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1", "Muscular Dystrophy-Dystroglycanopathy (Limb-Girdle), Type C, 1", "muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 1", "Limb-girdle muscular dystrophy-intellectual disability syndrome", "limb-girdle muscular dystrophy-intellectual disability syndrome", "Limb girdle muscular dystrophy with intellectual disability syndrome", "Autosomal recessive limb girdle muscular dystrophy type 2K (disorder)", "Muscular Dystrophy, Limb-Girdle, Autosomal Recessive, With Mental Retardation", "autosomal recessive limb-girdle muscular dystrophy caused by mutation in POMT1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive limb-girdle muscular dystrophy type 2K", "shortest_name_length": 6}
{"curie": "UMLS:C0031085", "names": ["Parodontal abscess", "ABSCESS PARADONTAL", "Paradontal abscess", "Peridental abscess", "ABSCESS PERIODONTAL", "PERIODONTAL ABSCESS", "peridental; abscess", "periodontal abscess", "abscess; peridental", "Periodontal Abscess", "paradontal; abscess", "Periodontal abscess", "Abscess periodontal", "periodontal; abscess", "Abscess, Periodontal", "abscess; periodontal", "Periodontal Abscesses", "Abscesses, Periodontal", "Lateral alveolar abscess", "Parietal abscess of tooth", "Lateral periodontal abscess", "Periodontal abscess (disorder)", "periodontal abscess (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Periodontal Abscess", "shortest_name_length": 18}
{"curie": "UMLS:C5670995", "names": ["Granular Cell Glioblastoma", "Granular Cell Astrocytoma/Glioblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Granular Cell Glioblastoma", "shortest_name_length": 26}
{"curie": "MONDO:0017070", "names": ["total spina bifida cystica"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "total spina bifida cystica", "shortest_name_length": 26}
{"curie": "MONDO:0011047", "names": ["Chitty Hall Baraitser syndrome", "Chitty-Hall-Baraitser syndrome", "chitty-Hall-Baraitser syndrome", "deafness, epiphyseal dysplasia, short stature", "Deafness-epiphyseal dysplasia-short stature syndrome", "deafness-epiphyseal dysplasia-short stature syndrome", "Hearing loss-epiphyseal dysplasia-short stature syndrome", "Deafness with epiphyseal dysplasia and short stature syndrome", "Deafness with epiphyseal dysplasia and short stature syndrome (disorder)", "Deafness, femoral epiphyseal dysplasia, short stature and developmental delay", "deafness, femoral epiphyseal dysplasia, short stature and developmental delay", "Growth retardation, deafness, femoral epiphyseal dysplasia, and lacrimal duct obstruction", "growth retardation, deafness, femoral epiphyseal dysplasia, and lacrimal duct obstruction", "GROWTH RETARDATION, DEAFNESS, FEMORAL EPIPHYSEAL DYSPLASIA, AND LACRIMAL DUCT OBSTRUCTION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness-epiphyseal dysplasia-short stature syndrome", "shortest_name_length": 30}
{"curie": "UMLS:C0333629", "names": ["Hemosiderin Deposition", "Hemosiderin deposition", "hemosiderin deposition", "Haemosiderin deposition", "Hemosiderin pigmentation", "hemosiderin pigmentation", "Pigmentation, hemosiderin", "Hemosiderin Pigmentations", "Haemosiderin pigmentation", "Hemosiderin deposition, NOS", "Hemosiderin pigmentation, NOS", "Hemosiderin pigmentation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemosiderin pigmentation", "shortest_name_length": 22}
{"curie": "MONDO:0013296", "names": ["SCLL", "8p11 Stem Cell Syndrome", "8p11 stem cell syndrome", "Stem cell leukemia/lymphoma", "STEM CELL LEUKEMIA/LYMPHOMA", "stem cell leukemia/lymphoma", "8p11 Myeloproliferative Syndrome", "8p11 myeloproliferative syndrome", "8p11 stem cell lymphoma/leukemia syndrome", "8p11 Stem Cell Leukemia/Lymphoma Syndrome", "8p11 stem cell leukemia/lymphoma syndrome", "8p11 Stem Cell Lymphoma/Leukemia Syndrome", "chromosome 8p11 myeloproliferative syndrome", "CHROMOSOME 8p11 MYELOPROLIFERATIVE SYNDROME", "Myeloid/Lymphoid Neoplasms with FGFR1 Rearrangement", "myeloid/lymphoid neoplasms with FGFR1 rearrangement", "Myeloid and lymphoid neoplasm with FGFR1 abnormality", "myeloid neoplasm associated with FGFR1 rearrangement", "myeloid and lymphoid neoplasms with FGFR1 rearrangement", "Myeloid and Lymphoid Neoplasms with FGFR1 Rearrangement", "Myeloid and lymphoid neoplasms with FGFR1 abnormalities", "Myeloid/lymphoid neoplasm associated with FGFR1 rearrangement", "myeloid/lymphoid neoplasm associated with FGFR1 rearrangement", "myeloid & lymphoid neoplasm w/ fibroblast growth factor receptor 1 abnormality", "Myeloid and lymphoid neoplasm with fibroblast growth factor receptor 1 abnormality", "Myeloid and lymphoid neoplasm with fibroblast growth factor receptor 1 abnormality (disorder)", "Myeloid and lymphoid neoplasm with fibroblast growth factor receptor 1 abnormality (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myeloid neoplasm associated with FGFR1 rearrangement", "shortest_name_length": 4}
{"curie": "MONDO:0014760", "names": ["IMD46", "IMMUNODEFICIENCY 46", "immunodeficiency 46", "immunodeficiency type 46", "CID due to TFRC deficiency", "TFRC-related combined immunodeficiency", "Combined immunodeficiency due to TFRC deficiency", "combined immunodeficiency due to TFRC deficiency", "TFRC (transferrin receptor) related combined immunodeficiency", "Combined immunodeficiency due to transferrin receptor deficiency", "Combined immunodeficiency due to transferrin receptor deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "TFRC-related combined immunodeficiency", "shortest_name_length": 5}
{"curie": "UMLS:C5420441", "names": ["Maxillofacial Desmoplastic Fibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Maxillofacial Desmoplastic Fibroma", "shortest_name_length": 34}
{"curie": "MONDO:0007151", "names": ["Arms, Malformation of", "ARMS, MALFORMATION OF", "arms, malformation of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arms, malformation of", "shortest_name_length": 21}
{"curie": "UMLS:C0038824", "names": ["injury; cornea, superficial", "cornea; injury, superficial", "injury; superficial, cornea", "Superficial injury of cornea", "Superficial Injury of Cornea", "Superficial injury of cornea (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Superficial injury of cornea", "shortest_name_length": 27}
{"curie": "MONDO:0002625", "names": ["bone Ewing sarcoma", "bone Ewing's sarcoma", "Bone Ewing's Sarcoma", "Ewing's tumor of bone", "Ewing Sarcoma of Bone", "osseous Ewing's tumor", "Osseous Ewing sarcoma", "Osseous Ewing's Tumor", "Ewing sarcoma of bone", "skeletal Ewing's tumor", "Skeletal Ewing sarcoma", "Skeletal Ewing's Tumor", "Ewing's Sarcoma of Bone", "Osseous Ewing's Sarcoma", "Ewing's sarcoma of bone", "osseous Ewing's sarcoma", "Skeletal Ewing's Sarcoma", "Ewing's sarcoma, osseous", "skeletal Ewing's sarcoma", "Ewing's Sarcoma, Osseous", "bone tissue Ewing sarcoma", "Localized Bone Ewing Sarcoma", "bone localized Ewing sarcoma", "Localized Bone Ewing's Sarcoma", "bone localized Ewing's sarcoma", "Localized Ewing's Sarcoma of Bone", "Localized Osseous Ewing's Sarcoma", "localized Skeletal Ewing's sarcoma", "localized skeletal Ewing's sarcoma", "Ewing's sarcoma of bone (disorder)", "Localized Skeletal Ewing's Sarcoma", "Ewing's sarcoma of bone (diagnosis)", "Localized Ewing's Sarcoma of the Bone", "Ewing's sarcoma/bone peripheral primitive neuroectodermal tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ewing sarcoma of bone", "shortest_name_length": 18}
{"curie": "UMLS:C0855235", "names": ["Feelings of worthlessness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Feelings of worthlessness", "shortest_name_length": 25}
{"curie": "MONDO:0012195", "names": ["DA4", "DAIID", "arthrogryposis distal type 4", "Distal arthrogryposis type 4", "distal arthrogryposis type 4", "ARTHROGRYPOSIS, DISTAL, TYPE 4", "distal arthrogryposis type IID", "Distal arthrogryposis type IID", "arthrogryposis, distal, type 4", "Arthrogryposis, Distal, Type 4", "arthrogryposis, distal, type 2D", "Arthrogryposis, Distal, Type Iid", "ARTHROGRYPOSIS, DISTAL, TYPE IID", "arthrogryposis with Severe scoliosis", "Arthrogryposis with severe scoliosis", "ARTHROGRYPOSIS WITH SEVERE SCOLIOSIS", "Arthrogryposis With Severe Scoliosis", "Distal arthrogryposis type 4 (disorder)", "arthrogryposis distal type 4 (diagnosis)", "Arthrogryposis-severe scoliosis syndrome", "arthrogryposis-severe scoliosis syndrome", "ARTHROGRYPOSIS, DISTAL, TYPE 4 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis-severe scoliosis syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0013218", "names": ["EVR5", "exudative vitreoretinopathy 5", "EXUDATIVE VITREORETINOPATHY 5", "Exudative Vitreoretinopathy 5", "exudative vitreoretinopathy type 5", "TSPAN12 exudative vitreoretinopathy", "exudative vitreoretinopathy caused by mutation in TSPAN12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exudative vitreoretinopathy 5", "shortest_name_length": 4}
{"curie": "UMLS:C3203555", "names": ["Maternal exposure during pregnancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Maternal exposure during pregnancy", "shortest_name_length": 34}
{"curie": "MONDO:0011775", "names": ["NPC", "Npca", "NPCA1", "nasopharyngeal cancer", "nasopharyngeal carcinoma", "nasopharyngeal carcinoma 1", "TP53 nasopharyngeal carcinoma", "nasopharyngeal carcinoma, somatic", "nasopharyngeal carcinoma, susceptibility to, 1", "NASOPHARYNGEAL CARCINOMA, SUSCEPTIBILITY TO, 1", "nasopharyngeal carcinoma caused by mutation in TP53"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasopharyngeal carcinoma, susceptibility to, 1", "shortest_name_length": 3}
{"curie": "UMLS:C4553788", "names": ["Stage IV Renal Pelvis Cancer", "Stage IV Renal Pelvis Cancer AJCC v8", "Stage IV Renal Pelvis Urothelial Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Renal Pelvis Cancer AJCC v8", "shortest_name_length": 28}
{"curie": "EFO:0000625", "names": ["nevus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nevus", "shortest_name_length": 5}
{"curie": "UMLS:C4288593", "names": ["Nodular Fasciitis-like Stroma Variant Thyroid Gland Papillary Cancer", "Nodular Fasciitis-Like Stroma Variant Thyroid Gland Papillary Carcinoma", "Thyroid Gland Papillary Carcinoma with Fibromatosis/Fasciitis-Like Stroma", "Thyroid Gland Papillary Carcinoma with Fibromatosis/Fasciitis-Like/Desmoid-Type Stroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Papillary Carcinoma with Fibromatosis/Fasciitis-Like/Desmoid-Type Stroma", "shortest_name_length": 68}
{"curie": "MONDO:0001592", "names": ["Genital prolapse", "prolapse genital", "genital prolapse", "prolapse; genital", "genital; prolapse", "Genital prolapse NOS", "Genital prolapse, NOS", "Female pelvic organ prolapse", "genital prolapse (diagnosis)", "prolapse of female genital organ", "Other specified genital prolapse", "Prolapse of female genital organs", "PROLAPSE OF THE FEMALE GENITAL ORGANS", "Prolapse of female genital organs, NOS", "Prolapse of female genital organs (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prolapse of female genital organ", "shortest_name_length": 16}
{"curie": "MONDO:0007605", "names": ["FIBRINOLYTIC DEFECT", "Fibrinolytic Defect", "fibrinolytic defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibrinolytic defect", "shortest_name_length": 19}
{"curie": "UMLS:C1332288", "names": ["Grade III Secondary Supratentorial Astrocytoma", "Secondary Supratentorial Anaplastic Astrocytoma", "Anaplastic Secondary Supratentorial Astrocytoma", "Grade 3 Secondary Supratentorial Astrocytic Tumor", "Grade III Secondary Supratentorial Astrocytic Tumor", "Grade 3 Secondary Supratentorial Astrocytic Neoplasm", "Undifferentiated Secondary Supratentorial Astrocytoma", "Grade III Secondary Supratentorial Astrocytic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary Supratentorial Anaplastic Astrocytoma", "shortest_name_length": 46}
{"curie": "UMLS:C3273080", "names": ["Non-Neoplastic Hepatobiliary Disorder", "Non-Neoplastic Liver and Biliary Disorder", "Non-Neoplastic Liver and Biliary System Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Hepatobiliary Disorder", "shortest_name_length": 37}
{"curie": "MONDO:0016607", "names": ["HPPA", "HPPO", "mild hypophosphatasia", "Adult Rathbun disease", "Adult hypophosphatasia", "adult hypophosphatasia", "Odontohypophosphatasia", "ODONTOHYPOPHOSPHATASIA", "Hypophosphatasia, Mild", "odontohypophosphatasia", "HYPOPHOSPHATASIA, MILD", "Hypophosphatasia, Adult", "HYPOPHOSPHATASIA, ADULT", "Hypophosphatasia, adult type", "Adult phosphoethanolaminuria", "Odontohypophosphatasia (disorder)", "Adult hypophosphatasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "odontohypophosphatasia", "shortest_name_length": 4}
{"curie": "MONDO:0100036", "names": ["variable age onset epilepsy", "variable age at onset electroclinical syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "variable age onset epilepsy", "shortest_name_length": 27}
{"curie": "UMLS:C5446668", "names": ["Refractory Adenoid Cystic Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Adenoid Cystic Carcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C1708502", "names": ["Induced Cataract", "Induced cataract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Induced cataract", "shortest_name_length": 16}
{"curie": "MONDO:0019639", "names": ["Megacalycosis", "Megacalycosis (disorder)", "congenital megacalycosis", "Dilatation of calyx without dilatation of pelvis and ureter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital megacalycosis", "shortest_name_length": 13}
{"curie": "UMLS:C0854707", "names": ["ASK", "arsenical keratoses", "Arsenical Keratosis", "Arsenical keratosis", "arsenical; keratosis", "keratosis; arsenical", "Arsenical keratosis (disorder)", "arsenical keratoses (diagnosis)", "Arsenical keratosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arsenical keratosis", "shortest_name_length": 3}
{"curie": "UMLS:C4526711", "names": ["Occult Lung Cancer", "Occult Lung Cancer AJCC v8", "Occult Lung Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Occult Lung Cancer AJCC v8", "shortest_name_length": 18}
{"curie": "MONDO:0002320", "names": ["congenital neurologic anomaly", "Congenital Nervous System Disorder", "congenital nervous system disorder", "congenital nervous system abnormality", "Other nervous system congenital anomalies", "congenital abnormality of the nervous system", "Other congenital anomalies of nervous system", "Congenital Abnormality of the Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital nervous system disorder", "shortest_name_length": 29}
{"curie": "UMLS:C4289321", "names": ["FIGO Stage IC3 Ovarian Cancer", "FIGO Stage IC3 Ovarian Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Stage IC3 Ovarian Cancer", "shortest_name_length": 29}
{"curie": "MONDO:0000483", "names": ["oculogyric crisis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculogyric crisis", "shortest_name_length": 17}
{"curie": "UMLS:C0333262", "names": ["vesicle", "Vesicle", "VESICLE", "VESICLES", "Vesicles", "vesicles", "Vesicle formation", "Vesicle (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vesicle (morphologic abnormality)", "shortest_name_length": 7}
{"curie": "UMLS:C5420145", "names": ["Refractory Non-Cutaneous Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Non-Cutaneous Melanoma", "shortest_name_length": 33}
{"curie": "MONDO:0021284", "names": ["ureter cancer stage 0is", "stage 0is ureter cancer", "Ureter Cancer Stage 0is", "Stage 0is Ureter Cancer", "Ureter Carcinoma in situ", "ureter carcinoma in situ", "stage 0 ureter carcinoma", "ureter in situ carcinoma", "stage 0is ureter carcinoma", "ureteral carcinoma in situ", "Stage 0is Ureter Carcinoma", "Ureteral Carcinoma in situ", "Carcinoma in situ of ureter", "carcinoma in situ of ureter", "Carcinoma in situ of Ureter", "Stage 0is Ureteral Carcinoma", "stage 0is ureteral carcinoma", "Stage 0is Carcinoma of Ureter", "stage 0is carcinoma of ureter", "carcinoma in situ of the ureter", "stage 0is ureter cancer aJCC v7", "Carcinoma in situ of the Ureter", "Stage 0is Ureter Cancer AJCC v7", "stage 0is carcinoma of the ureter", "Stage 0is Carcinoma of the Ureter", "CIS - Carcinoma in situ of ureter", "stage 0is ureter urothelial cancer", "Stage 0is Ureter Urothelial Carcinoma", "stage 0is ureter urothelial carcinoma", "Carcinoma in situ of ureter (disorder)", "carcinoma in situ of ureter (diagnosis)", "Stage 0is Ureter Urothelial Carcinoma AJCC v7", "stage 0is ureter urothelial carcinoma aJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma in situ of ureter", "shortest_name_length": 23}
{"curie": "UMLS:C0277120", "names": ["infection by Ancylostoma ceylanicum", "Ancylostomiasis due to Ancylostoma ceylonicum", "Ancylostomiasis due to Ancylostoma Ceylanicum", "Ancylostomiasis due to ancylostoma ceylanicum", "infection by Ancylostoma ceylanicum (diagnosis)", "Ancylostomiasis caused by Ancylostoma ceylonicum", "Ancylostomiasis due to Ancylostoma ceylonicum (disorder)", "Ancylostomiasis caused by Ancylostoma ceylonicum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ancylostomiasis due to Ancylostoma ceylonicum (disorder)", "shortest_name_length": 35}
{"curie": "MONDO:0014223", "names": ["ALS19", "ALS19 (diagnosis)", "AMYOTROPHIC LATERAL SCLEROSIS 19", "amyotrophic lateral sclerosis 19", "amyotrophic lateral sclerosis ALS19", "ERBB4 amyotrophic lateral sclerosis", "amyotrophic lateral sclerosis type 19", "amyotrophic lateral sclerosis caused by mutation in ERBB4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyotrophic lateral sclerosis type 19", "shortest_name_length": 5}
{"curie": "MONDO:0010782", "names": ["MLASA3", "myopathy, lactic acidosis, and sideroblastic anemia 3", "MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 3", "myopathy, lactic acidosis, and sideroblastic anemia type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy, lactic acidosis, and sideroblastic anemia 3", "shortest_name_length": 6}
{"curie": "MONDO:0032633", "names": ["MC1DN29", "nuclear type mitochondrial complex I deficiency 29", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 29", "mitochondrial complex 1 deficiency, nuclear type 29"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 29", "shortest_name_length": 7}
{"curie": "MONDO:0019858", "names": ["idiopathic congenital hypothyroidism", "Idiopathic congenital hypothyroidism", "Idiopathic congenital hypothyroidism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic congenital hypothyroidism", "shortest_name_length": 36}
{"curie": "UMLS:C4683609", "names": ["Lugano Classification Stage II Adult Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage II Adult Hodgkin Lymphoma AJCC v8", "shortest_name_length": 61}
{"curie": "MONDO:0022740", "names": ["Christian Johnson angenieta syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Christian Johnson angenieta syndrome", "shortest_name_length": 36}
{"curie": "MONDO:0018050", "names": ["SHFLD", "TH-SHFM", "SHFLD syndrome", "aplasia of tibia with ectrodactyly", "tibial aplasia-ectrodactyly syndrome", "tibial hemimelia-ectrodactyly syndrome", "ectrodactyly with aplasia of long bones", "SHFM associated with aplasia of long bones", "tibial hemimelia with split hand/foot malformation", "tibial aplasia with split-hand/split-foot deformity", "aplasia of tibia with split-hand/split-foot deformity", "split-hand/foot malformation with long bone deficiency", "split hand/foot malformation with long bone deficiency", "split-hand/foot malformation associated with aplasia of long bones"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tibial aplasia-ectrodactyly syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0018346", "names": ["FCCS", "NEDEPH", "Ferro-cerebro-cutaneous syndrome", "ferro-cerebro-cutaneous syndrome", "FERRO-CEREBRO-CUTANEOUS SYNDROME", "Ferro-cerebro-cutaneous syndrome (disorder)", "cerebro-cutaneous syndrome with iron overload", "Cerebro-cutaneous syndrome with iron overload", "NEURODEVELOPMENTAL DISORDER WITH EPILEPSY AND HEMOCHROMATOSIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ferro-cerebro-cutaneous syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0002265", "names": ["Stimming", "Stereotypy", "stereotypy", "stereotypes", "Stereotyped", "Stereotypies", "stereotypies", "Stereotypes NOS", "Motor stereotypy", "Motor Stereotypy", "Motor stereotypies", "repetitive behavior", "Stereotyped movement", "Stereotyped routines", "stereotyped movement", "Stereotypic behavior", "stereotyped behavior", "Stereotyped Behavior", "Stereotyped behavior", "Stereotyped response", "Repetitive movements", "Behavior, Stereotyped", "Stereotypic behaviour", "Stereotyped behaviors", "disorder; stereotyped", "Stereotypic behaviors", "Stereotyped behaviour", "Stereotyped movements", "stereotyped; disorder", "Stereotyped Behaviors", "movements stereotyped", "Stereotyped behaviours", "Stereotypical behavior", "stereotypies; disorder", "Stereotypic behaviours", "Behaviors, Stereotyped", "Stereotypical behaviors", "stereotypy habit disorder", "Stereotypy habit disorder", "Stereotypy/habit disorder", "Stereotypical motor behavior", "Stereotypic Movement Disorder", "stereotypic movement disorder", "stereotyped movement disorder", "Stereotypic movement disorder", "Stereotyped movement disorder", "Stereotypical motor behaviors", "Movement Disorder, Stereotypic", "Stereotypical motor behaviours", "Stereotyped routines (finding)", "Abnormal repetitive mannerisms", "Stereotypic Movement Disorders", "Stereotyped movement disorders", "stereotyped; movement disorders", "Repetitive stereotyped movement", "movement; disorder, stereotyped", "Stereotyped, repetitive behavior", "stereotyped repetitive movements", "Stereotyped repetitive movements", "Stereotyped, repetitive behaviour", "Stereotypy habit disorder (disorder)", "Repetitive or self-injurious behavior", "Repetitive or self-injurious behaviour", "Voluntary repetitive stereotyped movement", "Repetitive behaviour Stereotypic behavior", "stereotypic movement disorder (diagnosis)", "stereotyped repetitive movements NOS (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stereotypic movement disorder", "shortest_name_length": 8}
{"curie": "MONDO:0032943", "names": ["NSDVS2", "NEDMACE", "nabais sa-de vries syndrome, type 2", "NABAIS SA-DE VRIES SYNDROME, TYPE 2", "NEURODEVELOPMENTAL DISORDER WITH RELATIVE MACROCEPHALY AND WITH OR WITHOUT CARDIAC OR ENDOCRINE ANOMALIES", "neurodevelopmental disorder with relative macrocephaly and with or without cardiac or endocrine anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with relative macrocephaly and with or without cardiac or endocrine anomalies", "shortest_name_length": 6}
{"curie": "MONDO:0011815", "names": ["HYT3", "Hyt3", "hypertension, essential, susceptibility to, 3", "HYPERTENSION, ESSENTIAL, SUSCEPTIBILITY TO, 3", "hypertension, essential, susceptibility to, type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertension, essential, susceptibility to, 3", "shortest_name_length": 4}
{"curie": "UMLS:C1335756", "names": ["Reproductive Endocrine Neoplasm", "Reproductive System Endocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reproductive Endocrine Neoplasm", "shortest_name_length": 31}
{"curie": "UMLS:C1334451", "names": ["Lung Myolipoma", "Myolipoma of Lung", "Pulmonary Myolipoma", "Myolipoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Myolipoma", "shortest_name_length": 14}
{"curie": "MONDO:0020443", "names": ["absence of innominate vein", "absence of brachiocephalic vein"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "absence of innominate vein", "shortest_name_length": 26}
{"curie": "UMLS:C4552682", "names": ["stage I ureter cancer", "Stage I Ureter Cancer", "Stage I Ureter Cancer AJCC v8", "stage I ureter cancer AJCC v8", "Stage I Ureter Urothelial Carcinoma AJCC v8", "stage I ureter urothelial carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Ureter Cancer AJCC v8", "shortest_name_length": 21}
{"curie": "UMLS:C5204698", "names": ["Unresectable Gastric Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Gastric Carcinoma", "shortest_name_length": 30}
{"curie": "UMLS:C5205937", "names": ["Double Negative Prostate Cancer", "Double-Negative Prostate Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Double-Negative Prostate Carcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C3854430", "names": ["Graft versus host disease in GI tract", "Graft versus host disease in gastrointestinal tract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Graft versus host disease in gastrointestinal tract", "shortest_name_length": 37}
{"curie": "UMLS:C1336462", "names": ["Stage I Liver Cancer", "Stage I Liver Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Liver Carcinoma", "shortest_name_length": 20}
{"curie": "MONDO:0008444", "names": ["SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND DEMENTIA", "spastic paraplegia, optic atrophy, and dementia", "Spastic Paraplegia, Optic Atrophy, And Dementia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic paraplegia, optic atrophy, and dementia", "shortest_name_length": 47}
{"curie": "MONDO:0000840", "names": ["DON", "Dysbaric osteonecrosis", "dysbaric osteonecrosis", "caisson disease of bone", "Caisson disease of bone", "Dysbaric osteonecrosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dysbaric osteonecrosis", "shortest_name_length": 3}
{"curie": "MONDO:0004795", "names": ["SWIMMER EAR", "swimmer ear", "Infective OE", "swimmers ear", "ear swimmers", "Swimmers ear", "swimmer's Ear", "ears swimmers", "swimmer's ear", "Swimmer's Ear", "ear swimmer's", "Swimmer's ear", "Otitis externa", "Otitis Externa", "externa otitis", "otitis externa", "OTITIS EXTERNA", "Otitis external", "externa; otitis", "external otitis", "External Otitis", "Externa, Otitis", "otitis external", "otitis; externa", "Otitis, External", "External Otitides", "Otitis externa NOS", "Otitides, External", "outer Ear infection", "Outer Ear Infection", "OE - Otitis externa", "Otitis externa, NOS", "external Ear infection", "External Ear Infection", "Infective otitis externa", "infective otitis externa", "infectious otitis externa", "external ear inflammation", "Infectious Otitis Externa", "Inflammation of ear canal", "infective; otitis externa", "External Ear Inflammation", "External ear inflammation", "Otitis externa (disorder)", "Inflammation, External Ear", "External Ear Inflammations", "Unspecified otitis externa", "otitis; externa, infective", "Ear Inflammation, External", "otitis externa (diagnosis)", "inflammation; ear, external", "Otitis externa, unspecified", "ear; inflammation, external", "Infective otitis externa NOS", "Infective otitis externa, NOS", "Infective otitis externa (disorder)", "infective otitis externa (diagnosis)", "inflammation; external auditory canal", "external auditory canal; inflammation", "Infective otitis externa, unspecified", "Inflammation of External Auditory Canal", "Inflammation of the External Auditory Canal", "Unspecified otitis externa, unspecified ear", "external ear inflammation (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "otitis externa", "shortest_name_length": 11}
{"curie": "UMLS:C4331408", "names": ["Thoracic and Lumbosacral Spinal Cord Ependymal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thoracic and Lumbosacral Spinal Cord Ependymal Tumor", "shortest_name_length": 52}
{"curie": "MONDO:0019098", "names": ["purpura; hemorrhage", "hemorrhage; purpura", "PURPURA HEMORRHAGICA", "Purpura Hemorrhagica", "hemorrhagica purpura", "Purpura hemorrhagica", "hemorrhagic; purpura", "purpura; hemorrhagic", "purpura haemorrhagica", "Purpura haemorrhagica", "Hemorrhagica, Purpura", "Immune thrombocytopenia", "Idiopathic thrombocytopenia", "Autoimmune thrombocytopenia", "idiopathic thrombocytopenia", "autoimmune thrombocytopenia", "Thrombocytopenia, autoimmune", "idiopathic; thrombocytopenia", "thrombocytopenia; idiopathic", "Immune-mediated thrombocytopenia", "THROMBOCYTOPENIC PURPURA CHRONIC", "thrombocytopenic purpura chronic", "Chronic thrombocytopenic purpura", "Idiopathic thrombocytopenic purpura", "ITP Immune-mediated thrombocytopenia", "Chronic thrombocytopenic purpura, NOS", "Primary ITP (immune thrombocytopenia)", "Autoimmune thrombocytopenia (disorder)", "Chronic idiopathic thrombocytopenic purpura", "chronic idiopathic thrombocytopenic purpura", "Idiopathic thrombocytopenic purpura, chronic", "Chronic idiopathic thrombocytopenic purpura, NOS", "Chronic idiopathic thrombocytopenic purpura (disorder)", "chronic idiopathic thrombocytopenic purpura (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune thrombocytopenia", "shortest_name_length": 19}
{"curie": "MONDO:0001011", "names": ["Breast cyst", "BREAST CYST", "breast cyst", "Breast Cyst", "Cyst breast", "cyst; breast", "Cyst, Breast", "breast; cyst", "breast cysts", "Breast Cysts", "Cyst;breast;F", "Cysts, Breast", "cyst of breast", "Cyst of Breast", "Cyst of breast", "cysts on breast", "Breast atheroma", "Cyst of the breast", "cyst of the breast", "Cyst of the Breast", "Cyst of breast, NOS", "breast cyst (diagnosis)", "Breast atheromatous cyst", "Cyst of breast (disorder)", "cysts on breast (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast cyst", "shortest_name_length": 11}
{"curie": "UMLS:C1335450", "names": ["Posterior Pharyngeal Wall Carcinoma", "Posterior Pharyngeal Wall Throat Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Posterior Pharyngeal Wall Carcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C3272411", "names": ["Gastric MANEC", "Gastric Mixed Adenoneuroendocrine Carcinoma", "Gastric (Stomach) Mixed Adenoneuroendocrine Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Mixed Adenoneuroendocrine Carcinoma", "shortest_name_length": 13}
{"curie": "MONDO:0021282", "names": ["testis malignant teratoma", "immature teratoma of testis", "Immature Teratoma of Testis", "malignant teratoma of testis", "Malignant Teratoma of Testis", "testicular immature teratoma", "Malignant teratoma of testis", "Immature Testicular Teratoma", "Testicular Immature Teratoma", "immature testicular teratoma", "testicular malignant teratoma", "malignant testicular teratoma", "Testicular malignant teratoma", "Malignant Testicular Teratoma", "Testicular Malignant Teratoma", "immature teratoma of the testis", "Immature Teratoma of the Testis", "Malignant Teratoma of the Testis", "malignant teratoma of the testis", "Malignant teratoma of testis (disorder)", "malignant teratoma of testis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant teratoma of testis", "shortest_name_length": 25}
{"curie": "UMLS:C1336427", "names": ["Stage IV Nasal Cavity Cancer", "Stage IV Nasal Cavity Carcinoma", "Stage IV Carcinoma of Nasal Cavity", "Stage IV Carcinoma of the Nasal Cavity", "Stage IV Nasal Cavity Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Nasal Cavity Cancer", "shortest_name_length": 28}
{"curie": "UMLS:C4552284", "names": ["Gallbladder hypofunction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gallbladder hypofunction", "shortest_name_length": 24}
{"curie": "MONDO:0016961", "names": ["partial trisomy of chromosome 10q", "partial duplication of chromosome 10q", "partial trisomy of the long arm of chromosome 10", "partial duplication of the long arm of chromosome 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of the long arm of chromosome 10", "shortest_name_length": 33}
{"curie": "UMLS:C1332503", "names": ["Gastric Myoblastoma", "Myoblastoma of Stomach", "Myoblastoma of the Stomach", "Benign Gastric Granular Cell Tumor", "Benign Granular Cell Stomach Tumor", "benign gastric granular cell neoplasm", "Benign Gastric Granular Cell Neoplasm", "Benign Granular Cell Stomach Neoplasm", "Benign Granular Cell Tumor of Stomach", "benign granular cell neoplasm of stomach", "Benign Granular Cell Neoplasm of Stomach", "Benign Granular Cell Tumor of the Stomach", "Benign Granular Cell Neoplasm of the Stomach", "benign granular cell neoplasm of stomach (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Gastric Granular Cell Tumor", "shortest_name_length": 19}
{"curie": "UMLS:C5206681", "names": ["Unresectable Colorectal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Colorectal Carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0009190", "names": ["Epiphyseal Dysplasia of Femoral Head, Myopia, and Deafness", "EPIPHYSEAL DYSPLASIA OF FEMORAL HEAD, MYOPIA, AND DEAFNESS", "epiphyseal dysplasia of femoral head, myopia, and deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epiphyseal dysplasia of femoral head, myopia, and deafness", "shortest_name_length": 58}
{"curie": "MONDO:0011703", "names": ["spongiform encephalopathy with neuropsychiatric features", "SPONGIFORM ENCEPHALOPATHY WITH NEUROPSYCHIATRIC FEATURES", "Spongiform Encephalopathy with Neuropsychiatric Features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spongiform encephalopathy with neuropsychiatric features", "shortest_name_length": 56}
{"curie": "MONDO:0004150", "names": ["giant fibroadenoma", "Giant Fibroadenoma", "Giant fibroadenoma", "[M] Giant fibroadenoma", "giant breast fibroadenoma", "breast giant fibroadenoma", "Breast Giant Fibroadenoma", "Giant Breast Fibroadenoma", "Giant Fibroadenoma of Breast", "Giant fibroadenoma of breast", "Serocystic disease of Brodie", "giant fibroadenoma of breast", "giant fibroadenoma of the breast", "Giant adenofibroma of the breast", "Giant Fibroadenoma of the Breast", "Giant intracanalicular fibroadenoma", "Giant fibroadenoma of breast (disorder)", "Giant fibroadenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast giant fibroadenoma", "shortest_name_length": 18}
{"curie": "MONDO:0007644", "names": ["IGAD1", "IgAD1", "IgA, selective deficiency of", "Iga, selective deficiency of", "Immunoglobulin A Deficiency 1", "IMMUNOGLOBULIN A deficiency 1", "IMMUNOGLOBULIN A DEFICIENCY 1", "Immunoglobulin a deficiency 1", "Immunoglobulin A, selective deficiency of", "gamma-A-globulin, selective deficiency of", "Immunoglobulin a, selective deficiency of", "Gamma-a-globulin, selective deficiency of", "GAMMA-A-GLOBULIN, SELECTIVE DEFICIENCY OF", "immunoglobulin A deficiency, autosomal recessive, autosomal dominant, isolated cases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IgAD1", "shortest_name_length": 5}
{"curie": "UMLS:C4520747", "names": ["stage IV lip and oral cavity cancer", "Lip and Oral Cavity Cancer Stage IV", "Stage IV Lip and Oral Cavity Cancer", "Stage IV Lip and Oral Cavity Cancer v7", "Stage IV Lip and Oral Cavity Carcinoma", "Stage IV Lip and Oral Cavity Cancer v6", "Lip and Oral Cavity Carcinoma Stage IV", "Stage IV Lip and Oral Cavity Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Lip and Oral Cavity Cancer AJCC v6 and v7", "shortest_name_length": 35}
{"curie": "MONDO:0000704", "names": ["Lymphocytic Colitis", "colitis lymphocytic", "lymphocytic colitis", "Lymphocytic colitis", "Colitis, Lymphocytic", "Lymphocytic colitis (disorder)", "Lymphocytic-plasmacytic colitis", "lymphocytic colitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphocytic colitis", "shortest_name_length": 19}
{"curie": "UMLS:C0280781", "names": ["Pilocytic Astrocytoma", "adult pilocytic astrocytoma", "Adult Pilocytic Astrocytoma", "pilocytic astrocytoma, adult", "astrocytoma, adult noninfiltrating", "noninfiltrating astrocytoma, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Pilocytic Astrocytoma", "shortest_name_length": 21}
{"curie": "UMLS:C0152254", "names": ["steatosis", "Steatosis", "Fatty Change", "FATTY CHANGE", "fatty change", "Fatty change", "changes fatty", "Fatty changes", "fatty degeneration", "Fatty degeneration", "Fatty metamorphosis", "Degeneration, fatty", "Lipoid degeneration", "fatty metamorphosis", "Steatosis (disorder)", "Fatty degeneration (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fatty degeneration", "shortest_name_length": 9}
{"curie": "MONDO:0014755", "names": ["CSCSC2", "congenital symmetric circumferential skin creases 2", "symmetric circumferential skin creases, congenital, 2", "SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2", "skin creases, congenital symmetric circumferential, 2", "skin creases, congenital symmetric circumferential, type 2", "MAPRE2 multiple benign circumferential skin creases on limbs", "skin creases, congenital symmetric circumferential, 2; CSCSC2", "multiple benign circumferential skin creases on limbs caused by mutation in MAPRE2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin creases, congenital symmetric circumferential, 2", "shortest_name_length": 6}
{"curie": "UMLS:C1708774", "names": ["Lung Mixed Squamous and Glandular Papilloma", "Mixed squamous cell and glandular papilloma", "Lung Mixed Squamous Cell and Glandular Papilloma", "Bronchial Mixed Squamous Cell and Glandular Papilloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Mixed Squamous Cell and Glandular Papilloma", "shortest_name_length": 43}
{"curie": "MONDO:0003066", "names": ["submandibular adenitis", "Submandibular adenitis", "submandibular lymphadenitis", "Lymphadenitis submandibular", "Submandibular Lymphadenitis", "SUBMANDIBULAR LYMPHADENITIS", "Submandibular lymphadenitis", "lymphadenitis submandibular", "adenitis; submandibular gland", "Submandibular lymphadenitis (disorder)", "Submandibular lymphadenitis (diagnosis)", "submandibular gland lymphadenitis (disease)", "lymphadenitis (disease) of submandibular gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "submandibular adenitis", "shortest_name_length": 22}
{"curie": "UMLS:C1333033", "names": ["Chronic Allograft Arteriopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic Allograft Arteriopathy", "shortest_name_length": 30}
{"curie": "UMLS:C0243038", "names": ["Lewis Lung Carcinoma", "Lung Carcinoma, Lewis", "Carcinoma, Lewis Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carcinoma, Lewis Lung", "shortest_name_length": 20}
{"curie": "MONDO:0014237", "names": ["DFNB76", "autosomal recessive deafness 76", "deafness, autosomal recessive 76", "DEAFNESS, AUTOSOMAL RECESSIVE 76", "deafness, autosomal recessive type 76", "autosomal recessive nonsyndromic deafness 76", "SYNE4 autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 76", "autosomal recessive nonsyndromic deafness type 76", "autosomal recessive nonsyndromic deafness caused by mutation in SYNE4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 76", "shortest_name_length": 6}
{"curie": "MONDO:0016361", "names": ["isolated inherited macrothrombocytopenia", "isolated hereditary macrothrombocytopenia", "isolated inherited giant platelet disorder", "isolated hereditary giant platelet disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated hereditary giant platelet disorder", "shortest_name_length": 40}
{"curie": "MONDO:0022991", "names": ["Mosaic triploidy", "diploid-triploid mosaicism", "Diploid-Triploid Mosaicism", "diploid/triploid mosaicism", "diploid/triploid mixoploidy", "triploidy, diploidy, mixoploidy syndrome", "Triploidy, diploidy, mixoploidy syndrome", "Triploidy, diploidy, mixoploidy syndrome (disorder)", "triploidy, diploidy, mixoploidy syndrome (diagnosis)", "Growth retardation, truncal obesity, facial asymmetry, hypotonia, small phallus, malformed low-set ears and micrognathia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diploid-triploid mosaicism", "shortest_name_length": 16}
{"curie": "MONDO:0019140", "names": ["Akee poisoning", "ackee poisoning", "Ackee poisoning", "Jamaican vomiting sickness", "Jamaican vomiting syndrome", "acute ackee fruit intoxication", "Acute ackee fruit intoxication", "Acute intoxication by Blighia sapida", "acute intoxication by Blighia sapida", "Jamaican vomiting sickness (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute ackee fruit intoxication", "shortest_name_length": 14}
{"curie": "MONDO:0018244", "names": ["obesity due to SIM1 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "obesity due to SIM1 deficiency", "shortest_name_length": 30}
{"curie": "UMLS:C0278791", "names": ["refractory CLL", "Refractory CLL", "CLL, refractory", "Refractory Chronic Lymphoid Leukemia", "Chronic Lymphocytic Leukemia Refractory", "Refractory Chronic Lymphocytic Leukemia", "Chronic lymphocytic leukemia refractory", "refractory chronic lymphocytic leukemia", "Refractory Chronic Lymphogenous Leukemia", "chronic lymphocytic leukemia, refractory", "leukemia, refractory chronic lymphocytic", "Chronic lymphocytic leukaemia refractory", "lymphocytic leukemia, refractory chronic", "Refractory Chronic Lymphocytic Leukemia (CLL)", "Refractory B-Cell Chronic Lymphocytic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic lymphocytic leukemia refractory", "shortest_name_length": 14}
{"curie": "MONDO:0013444", "names": ["NPHP9", "NEPHRONOPHTHISIS 9", "nephronophthisis 9", "nephronophthisis type 9", "NEK8 nephronophthisis (disease)", "nephronophthisis (disease) caused by mutation in NEK8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephronophthisis 9", "shortest_name_length": 5}
{"curie": "MONDO:0016394", "names": ["ABSN", "sporadic IBSN", "acute bilateral striatal necrosis", "sporadic infantile striatonigral necrosis", "sporadic infantile striatonigral degeneration", "sporadic infantile bilateral striatal necrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sporadic infantile bilateral striatal necrosis", "shortest_name_length": 4}
{"curie": "UMLS:C1711169", "names": ["Appendix TSA", "Appendix Serrated Adenoma", "Appendix Serrated Adenoma Type II", "Appendix Traditional Serrated Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Appendix Traditional Serrated Adenoma", "shortest_name_length": 12}
{"curie": "MONDO:0023419", "names": ["prolinemia", "Prolinemia", "Hyperprolinemia", "hyperprolinemia", "hyperprolinaemia", "Hyperprolinaemia", "Hyperprolinemia, NOS", "hyperprolinemia type 1", "Hyperprolinemia (disorder)", "proline oxidase deficiency", "hyperprolinemia (diagnosis)", "proline hydrogenase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperprolinemia", "shortest_name_length": 10}
{"curie": "MONDO:0012702", "names": ["AIS5", "CELIAC6", "CELIAC DISEASE, SUSCEPTIBILITY TO, 6", "celiac disease, susceptibility to, 6", "autoimmune disease, susceptibility to, 5", "AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 5", "GLUTEN-SENSITIVE ENTEROPATHY, SUSCEPTIBILITY TO, 6", "gluten-sensitive enteropathy, susceptibility to, 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "celiac disease, susceptibility to, 6", "shortest_name_length": 4}
{"curie": "MONDO:0006845", "names": ["male genital tuberculosis", "Male Genital Tuberculoses", "Male Genital Tuberculosis", "Male genital Tuberculoses", "Tuberculosis, Male Genital", "genital tuberculosis, Male", "genital Tuberculoses, Male", "Tuberculoses, Male genital", "Genital Tuberculosis, Male", "Tuberculoses, Male Genital", "Genital Tuberculoses, Male", "GENITALIA, MALE, TUBERCULOSIS", "Male genital tract tuberculosis", "tuberculosis male genital organs", "Tuberculosis of male genital organs", "Male genital tract tuberculosis NOS", "male reproductive system tuberculosis", "tuberculosis male genital organs (diagnosis)", "Tuberculosis of male genital organs (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "male genital tuberculosis", "shortest_name_length": 25}
{"curie": "UMLS:C0855203", "names": ["Testicular germ cell tumor mixed stage I", "Stage I Testicular Mixed Germ Cell Tumor", "Testicular germ cell tumour mixed stage I", "Stage I Testicular Mixed Germ Cell Tumor AJCC v6", "Stage I Testicular Mixed Germ Cell Tumor AJCC v7", "Stage I Testicular Mixed Germ Cell Tumor AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular germ cell tumor mixed stage I", "shortest_name_length": 40}
{"curie": "MONDO:0015083", "names": ["nuclear oculomotor paralysis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nuclear oculomotor paralysis", "shortest_name_length": 28}
{"curie": "MONDO:0008403", "names": ["scalp defects postaxial polydactyly", "Scalp defects postaxial polydactyly", "SCALP DEFECTS AND POSTAXIAL POLYDACTYLY", "Scalp Defects And Postaxial Polydactyly", "scalp defects and postaxial polydactyly", "scalp defects-postaxial polydactyly syndrome", "Congenital scalp defects associated with postaxial polydactyly", "congenital scalp defects associated with postaxial polydactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scalp defects-postaxial polydactyly syndrome", "shortest_name_length": 35}
{"curie": "MONDO:0012371", "names": ["NS3", "Noonan Syndrome 3", "Noonan syndrome 3", "NOONAN SYNDROME 3", "KRAS Noonan syndrome", "Noonan syndrome type 3", "KRAS gene related Noonan syndrome", "Noonan syndrome caused by mutation in KRAS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Noonan syndrome 3", "shortest_name_length": 3}
{"curie": "MONDO:0014294", "names": ["Del(15)(q11.2)", "monosomy 15q11.2", "15q11.2 microdeletion", "Microdeletion 15q11.2", "chromosome 15q11.2 deletion", "15q11.2 microdeletion syndrome", "chromosome 15q11.2 microdeletion", "CHROMOSOME 15q11.2 DELETION SYNDROME", "Chromosome 15q11.2 deletion syndrome", "chromosome 15q11.2 deletion syndrome", "15q11.2 BP1-BP2 microdeletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 15q11.2 deletion syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0009154", "names": ["CHNG5", "congenital nongoitrous hypothyroidism 5", "congenital nongoitrous hypothryoidism 5", "hypothyroidism, congenital nongoitrous, 5", "hypothyroidism, congenital, nongoitrous, 5", "HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 5", "Hypothyroidism, Congenital, Nongoitrous, 5", "NKX2-5 hypothyroidism, congenital, nongoitrous", "hypothyroidism, congenital, nongoitrous, type 5", "hypothyroidism, congenital, nongoitrous caused by mutation in NKX2-5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypothyroidism, congenital, nongoitrous, 5", "shortest_name_length": 5}
{"curie": "UMLS:C3897060", "names": ["Contrasexual Sexual Development"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Contrasexual Sexual Development", "shortest_name_length": 31}
{"curie": "MONDO:0006346", "names": ["PAAC", "Pancreatic acinar cell cancer", "Pancreatic Acinar Cell Cancer", "Pancreatic acinar cell carcinoma", "pancreatic acinar cell carcinoma", "Pancreatic Acinar Cell Carcinoma", "Acinar Cell Carcinoma of Pancreas", "Acinar cell carcinoma of pancreas", "acinar cell carcinoma of pancreas", "pancreas acinar cell adenocarcinoma", "carcinoma of pancreatic acinar cell", "Pancreas Acinar Cell Adenocarcinoma", "Acinar Cell Carcinoma of the Pancreas", "acinar cell carcinoma of the pancreas", "pancreatic acinar cell adenocarcinoma", "Pancreatic Acinar Cell Adenocarcinoma", "Acinar Cell Adenocarcinoma of Pancreas", "acinar cell adenocarcinoma of pancreas", "adenocarcinoma, acinar cell, pancreatic", "Acinar Cell Adenocarcinoma of the Pancreas", "acinar cell adenocarcinoma of the pancreas", "pancreas cancer, acinar cell adenocarcinoma", "Acinar cell carcinoma of pancreas (disorder)", "pancreatic cancer, acinar cell adenocarcinoma", "acinar cell carcinoma of pancreas (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic acinar cell carcinoma", "shortest_name_length": 4}
{"curie": "UMLS:C0238408", "names": ["RECTUS SHEATH HEMATOMA", "Rectus sheath hematoma", "Rectus Sheath Hematoma", "rectus sheath hematoma", "rectus sheath haematoma", "Rectus sheath haematoma", "hematoma of rectus sheath", "Hematoma of rectus sheath", "Haematoma of rectus sheath", "Hematoma of rectus sheath (disorder)", "hematoma of rectus sheath (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hematoma of rectus sheath", "shortest_name_length": 22}
{"curie": "MONDO:0015234", "names": ["Kosztolanyi syndrome", "Arachnodactyly, abnormal ossification and mental retardation", "arachnodactyly, abnormal ossification and mental retardation", "arachnodactyly, abnormal ossification and intellectual disability", "arachnodactyly-abnormal ossification-intellectual disability syndrome", "Arachnodactyly-abnormal ossification-intellectual disability syndrome", "arachnodactyly with abnormal ossification and intellectual disability syndrome", "Arachnodactyly with abnormal ossification and intellectual disability syndrome", "Arachnodactyly with abnormal ossification and intellectual disability syndrome (disorder)", "arachnodactyly with abnormal ossification and intellectual disability syndrome (diagnosis)", "Syndrome of arachnodactyly, disturbance of cranial ossification, protruding eyes, feeding difficulties, and mental retardation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arachnodactyly-abnormal ossification-intellectual disability syndrome", "shortest_name_length": 20}
{"curie": "MONDO:0008907", "names": ["CDGIa", "CDG1A", "CDG-Ia", "CDG 1A", "CDG-IA", "CDG Ia", "Pmm2-CDG", "PMM2-CDG", "PMM2 deficiency", "JAEKEN SYNDROME", "Jaeken syndrome", "PMM2-CDG (CDG-Ia)", "CDG syndrome type Ia", "phosphomannomutase 2 deficiency", "Phosphomannomutase 2 deficiency", "PHOSPHOMANNOMUTASE 2 DEFICIENCY", "carbohydrate deficient glycoprotein 1", "congenital disorder of glycosylation 1a", "congenital disorder of glycosylation Ia", "PMM2-congenital disorder of glycosylation", "congenital disorder of glycosylation type Ia", "Congenital disorder of glycosylation type 1a", "Congenital disorder of glycosylation type 1A", "congenital disorder of glycosylation type 1a", "Congenital Disorder of Glycosylation Type Ia", "Congenital disorder of glycosylation type Ia", "Congenital Disorder of Glycosylation, Type Ia", "congenital disorder of glycosylation, type Ia", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia", "Carbohydrate-deficient glycoprotein syndrome type I", "Carbohydrate-Deficient Glycoprotein Syndrome Type Ia", "Carbohydrate deficient glycoprotein syndrome type Ia", "carbohydrate-deficient glycoprotein syndrome type 1A", "Carbohydrate-deficient glycoprotein syndrome type 1A", "carbohydrate deficient glycoprotein syndrome type Ia", "carbohydrate-deficient glycoprotein syndrome, type Ia", "Congenital disorder of glycosylation type Ia (disorder)", "CDG - Carbohydrate-deficient glycoprotein syndrome type I", "carbohydrate deficient glycoprotein (CDG) syndrome (CDGS) 1", "Carbohydrate-deficient glycoprotein syndrome type I (disorder)", "CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME, TYPE Ia, FORMERLY", "carbohydrate-deficient glycoprotein syndrome type 1A (formerly)", "carbohydrate-deficient glycoprotein syndrome, type Ia, formerly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PMM2-congenital disorder of glycosylation", "shortest_name_length": 5}
{"curie": "UMLS:C3897542", "names": ["Stage I Anaplastic Large Cell Lymphoma", "stage I childhood anaplastic large cell lymphoma", "Stage I Childhood Anaplastic Large Cell Lymphoma", "Ann Arbor Stage I Childhood Anaplastic Large Cell Lymphoma", "Ann Arbor Stage I Noncutaneous Childhood Anaplastic Large Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Childhood Anaplastic Large Cell Lymphoma", "shortest_name_length": 38}
{"curie": "UMLS:C1332613", "names": ["Breast Adenoacanthoma", "Adenoacanthoma of Breast", "Adenoacanthoma of the Breast", "breast adenocarcinoma with squamous metaplasia", "Breast Adenocarcinoma with Squamous Metaplasia", "Adenocarcinoma of Breast with Squamous Metaplasia", "adenocarcinoma of breast with squamous metaplasia", "Adenocarcinoma of the Breast with Squamous Metaplasia", "adenocarcinoma of breast with squamous metaplasia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenocarcinoma of breast with squamous metaplasia", "shortest_name_length": 21}
{"curie": "MONDO:0009849", "names": ["HIDS", "hyper-IgD syndrome", "Hyper IgD Syndrome", "Hyper-IgD Syndrome", "HYPER-IgD SYNDROME", "Hyper IgD syndrome", "Hyper-IgD syndrome", "hyper IgD syndrome", "Hyper-IgD Syndromes", "Hyper IgD Syndromes", "Syndrome, Hyper-IgD", "Hyperimmunoglobulinemia D", "periodic fever Dutch type", "periodic fever, Dutch type", "PERIODIC FEVER, DUTCH TYPE", "Periodic Fever, Dutch Type", "Periodic fever - Dutch type", "hyperimmunoglobulinemia D syndrome", "Hyperimmunoglobulinemia D syndrome", "partial mevalonate kinase deficiency", "Partial mevalonate kinase deficiency", "Hyperimmunoglobulin D with periodic fever", "Hyperimmunoglobinemia D with recurrent fever", "hyperimmunoglobinemia D with recurrent fever", "Hyperimmunoglobulinemia D with periodic fever", "hyperimmunoglobulinemia D with periodic fever", "Hyperimmunoglobulin D with periodic fever (finding)", "HYPERIMMUNOGLOBULINEMIA D AND PERIODIC FEVER SYNDROME", "hyperimmunoglobulinemia D and periodic fever syndrome", "Hyperimmunoglobulinemia D And Periodic Fever Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperimmunoglobulinemia D with periodic fever", "shortest_name_length": 4}
{"curie": "MONDO:0100147", "names": ["SAS", "SATB2-associated syndrome", "SATB2 associated disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SATB2 associated disorder", "shortest_name_length": 3}
{"curie": "UMLS:C3146266", "names": ["Stage III Esophageal Cancer", "Stage III Esophageal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Esophageal Cancer AJCC v7", "shortest_name_length": 27}
{"curie": "MONDO:0005185", "names": ["JRA", "chronic childhood arthritis", "Juvenile rheumatoid arthritis", "Juvenile Rheumatoid Arthritis", "Juvenile Rheumatoid Arthritis (AQ)", "Juvenile rheumatoid arthritis (AQ)", "Chronic arthritis of juvenile onset", "Chronic arthritis of juvenile onset (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic childhood arthritis", "shortest_name_length": 3}
{"curie": "UMLS:C0948102", "names": ["Sialadenoma", "salivary gland adenoma", "Salivary Gland Adenoma", "adenoma salivary gland", "Salivary gland adenoma", "adenoma glands salivary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Salivary gland adenoma", "shortest_name_length": 11}
{"curie": "UMLS:C0600178", "names": ["External Carotid Artery Diseases", "Arterial Diseases, External Carotid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "External Carotid Artery Diseases", "shortest_name_length": 32}
{"curie": "MONDO:0006092", "names": ["Appendix Villous Adenoma", "appendix villous adenoma", "Villous Adenoma of Appendix", "villous adenoma of appendix", "villous adenoma of the appendix", "Villous Adenoma of the Appendix", "vermiform appendix villous adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "appendix villous adenoma", "shortest_name_length": 24}
{"curie": "UMLS:C5419814", "names": ["Liver Small Cell Carcinoma", "Hepatic Small Cell Carcinoma", "Liver Small Cell Neuroendocrine Carcinoma", "Hepatic Small Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liver Small Cell Neuroendocrine Carcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0019998", "names": ["gastroduodenal malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastroduodenal malformation", "shortest_name_length": 27}
{"curie": "MONDO:0007568", "names": ["AAT4", "FAA4", "aortic aneurysm, familial thoracic 4", "AORTIC ANEURYSM, FAMILIAL THORACIC 4", "Aortic aneurysm, familial thoracic 4", "aortic aneurysm, familial thoracic type 4", "MYH11 familial thoracic aortic aneurysm and aortic dissection", "Aortic aneurysm-aortic dissection and patent ductus arteriosus", "aortic aneurysm/aortic dissection and patent ductus arteriosus", "AORTIC ANEURYSM/AORTIC DISSECTION AND PATENT DUCTUS ARTERIOSUS", "familial thoracic aortic aneurysm and aortic dissection caused by mutation in MYH11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic aneurysm, familial thoracic 4", "shortest_name_length": 4}
{"curie": "MONDO:0100132", "names": ["intrahepatic bile duct adenosquamous carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intrahepatic bile duct adenosquamous carcinoma", "shortest_name_length": 46}
{"curie": "MONDO:0023161", "names": ["Viral myocarditis", "viral myocarditis", "Viral Myocarditis", "myocarditis viral", "myocarditis; viral", "viral; myocarditis", "Viral perimyocarditis", "Myocarditis viral NOS", "Viral myocarditis, NOS", "Viral myocarditis (disorder)", "Viral myocarditis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "viral myocarditis", "shortest_name_length": 17}
{"curie": "MONDO:0012674", "names": ["ARMD10", "age related macular degeneration 10", "TLR4 age-related macular degeneration", "Macular Degeneration, Age-Related, 10", "MACULAR DEGENERATION, AGE-RELATED, 10", "macular degeneration, age-related, 10", "age related macular degeneration type 10", "macular Degeneration, age-related, type 10", "age-related macular degeneration caused by mutation in TLR4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "age related macular degeneration 10", "shortest_name_length": 6}
{"curie": "MONDO:0008623", "names": ["UNDRITZ ANOMALY", "Undritz anomaly", "Undritz Anomaly", "Hypersegmentation of Nuclei of Polymorphonuclear Leukocytes", "hypersegmentation of nuclei of polymorphonuclear leukocytes", "HYPERSEGMENTATION OF NUCLEI OF POLYMORPHONUCLEAR LEUKOCYTES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Undritz anomaly", "shortest_name_length": 15}
{"curie": "MONDO:0019727", "names": ["MC type III", "mixed cryoglobulinemia type III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed cryoglobulinemia type III", "shortest_name_length": 11}
{"curie": "MONDO:0004046", "names": ["Brain meningioma", "Brain Meningioma", "pediatric brain meningioma", "brain pediatric meningioma", "childhood brain meningioma", "Childhood Brain Meningioma", "pediatric meningioma of brain", "childhood meningioma of brain", "pediatric meningioma of the brain", "Childhood Intracranial Meningioma", "childhood meningioma of the brain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood brain meningioma", "shortest_name_length": 16}
{"curie": "UMLS:C1332044", "names": ["AIDS-Related Herpes Zoster"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Herpes Zoster", "shortest_name_length": 26}
{"curie": "UMLS:C5204261", "names": ["Peripheral Lung", "Peripheral Lung Parenchyma Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peripheral Lung Parenchyma Tumor", "shortest_name_length": 15}
{"curie": "MONDO:0014990", "names": ["UHS3", "UNCOMBABLE HAIR SYNDROME 3", "uncombable hair syndrome 3", "TCHH uncombable hair syndrome", "uncombable hair syndrome type 3", "uncombable hair syndrome 3; UHS3", "uncombable hair syndrome caused by mutation in TCHH"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uncombable hair syndrome 3", "shortest_name_length": 4}
{"curie": "UMLS:C0740386", "names": ["Anterior communicating artery aneurysm", "Anterior Communicating Artery Aneurysm", "anterior communicating artery aneurysm", "Aneurysm, Anterior Communicating Artery", "Aneurysm of anterior communicating artery", "aneurysm of anterior communicating artery", "Aneurysm of anterior communicating artery (disorder)", "aneurysm of anterior communicating artery (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aneurysm, Anterior Communicating Artery", "shortest_name_length": 38}
{"curie": "UMLS:C5556290", "names": ["Microsatellite Stable Ovarian Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Microsatellite Stable Ovarian Carcinoma", "shortest_name_length": 39}
{"curie": "MONDO:0005265", "names": ["IBD", "Chronic enteritis", "Chronic enteropathy", "IRRITABLE BOWEL DISEASE", "Autoimmune Bowel Disorder", "autoimmune bowel disorder", "Inflammatory Bowel Disease", "INFLAMMATORY BOWEL DISEASE", "inflammatory bowel disease", "Inflammatory bowel disease", "disease inflammatory bowel", "bowel disease inflammatory", "Disease;inflammatory bowel", "bowel diseases inflammatory", "Inflammatory bowel diseases", "Inflammatory Bowel Diseases", "inflammatory bowel diseases", "Bowel Diseases, Inflammatory", "Inflammatory bowel disease NOS", "Inflammation of large intestine", "Inflammatory bowel disease, NOS", "BOWEL INFLAMMATORY BOWEL DISEASE", "IBD - Inflammatory bowel disease", "IBD - inflammatory bowel disease", "Inflammation of the large intestine", "Inflammatory bowel disease (disorder)", "inflammatory bowel disease (diagnosis)", "Inflammation of large intestine (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory bowel disease", "shortest_name_length": 3}
{"curie": "MONDO:0015665", "names": ["Scleromyxedema", "scleromyxedema", "Scleromyxoedema", "scleromyxoedema", "Papular mucinosis", "papular mucinosis", "Papular Mucinosis", "mucinosis, papular", "Mucinosis, Papular", "Lichenoid myxedema", "Lichenoid myxoedema", "Lichen Myxedematosus", "Lichen myxedematosus", "lichen myxedematosus", "myxedematosus, lichen", "Lichen myxoedematosus", "Arndt-Gottron disease", "myxedematosus; lichen", "Myxedematosus, Lichen", "lichen; myxedematosus", "Arndt-Gottron syndrome", "Scleromyxedema (disorder)", "scleromyxedema (diagnosis)", "Localized lichen myxedematosus", "Lichen myxedematosus (disorder)", "generalized papular and sclerodermoid", "generalized lichenoid papular eruption", "Generalised lichenoid papular eruption", "Generalized lichenoid papular eruption", "Generalized papular and sclerodermoid lichen myxedematosus", "generalized papular and sclerodermoid lichen myxedematosus", "Generalised papular and sclerodermoid lichen myxoedematosus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scleromyxedema", "shortest_name_length": 14}
{"curie": "MONDO:0010669", "names": ["MF4", "Syndactyly type 8", "syndactyly type 8", "metacarpal 4-5 fusion", "4-5 metacarpal fusion", "Metacarpal 4 5 Fusion", "METACARPAL 4-5 FUSION", "metacarpals 4 and 5 fusion", "Syndactyly of fingers type 8", "Fusion of metacarpal 4 and 5", "Fusion of metacarpals 4 and 5", "fusion of metacarpals 4 and 5", "FGF16 non-syndromic syndactyly", "Syndactyly of fingers type 8 (disorder)", "metacarpal 4-5 fusion, X-linked recessive", "non-syndromic syndactyly caused by mutation in FGF16"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndactyly type 8", "shortest_name_length": 3}
{"curie": "MONDO:0002045", "names": ["Hydrocephaly communicative", "HYDROCEPHALY COMMUNICATIVE", "Communicating hydrocephalus", "communicating hydrocephalus", "Communicating Hydrocephalus", "HYDROCEPHALUS COMMUNICATING", "hydrocephalus; communicating", "Hydrocephalus, Communicating", "HYDROCEPHALUS, COMMUNICATING", "communicating; hydrocephalus", "Hydrocephalus, communicating", "non-obstructive hydrocephalus", "Non-Obstructive Hydrocephalus", "Communicating hydrocephalus (disorder)", "increased pressure communicating hydrocephalus", "increased pressure communicating hydrocephalus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "communicating hydrocephalus", "shortest_name_length": 26}
{"curie": "UMLS:C4553619", "names": ["Stage IVB Vaginal Cancer", "Stage IVB Vaginal Cancer AJCC v8", "Stage IVB Vaginal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Vaginal Cancer AJCC v8", "shortest_name_length": 24}
{"curie": "UMLS:C1332501", "names": ["Benign Fibrous Tumor", "Benign Fibrogenic Tumor", "Benign Fibrous Neoplasm", "Benign Fibrocytic Tumor", "Benign Fibroblastic Tumor", "Benign Fibrocytic Neoplasm", "Benign Fibrogenic Neoplasm", "Benign Fibroblastic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Fibroblastic Neoplasm", "shortest_name_length": 20}
{"curie": "UMLS:C0278850", "names": ["Stage II Papillary Thyroid Cancer", "stage II papillary thyroid cancer", "thyroid cancer, stage II papillary", "papillary thyroid cancer, stage II", "Stage II Thyroid Papillary Carcinoma", "Stage II Thyroid Gland Papillary Cancer", "Stage II Papillary Carcinoma of Thyroid", "Stage II Thyroid Gland Papillary Carcinoma", "Stage II Papillary Thyroid Gland Carcinoma", "Stage II Papillary Carcinoma of the Thyroid", "adenocarcinoma, papillary, thyroid, stage II", "Stage II Papillary Carcinoma of Thyroid Gland", "mixed adenocarcinoma of the thyroid, stage II", "Stage II Papillary Carcinoma of the Thyroid Gland", "papillary adenocarcinoma of the thyroid, stage II", "Stage II Thyroid Gland Papillary Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Thyroid Gland Papillary Carcinoma AJCC v7", "shortest_name_length": 33}
{"curie": "UMLS:C4684886", "names": ["Refractory Primary Cutaneous Lymphoma", "Refractory Primary Cutaneous (Skin) Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Primary Cutaneous Lymphoma", "shortest_name_length": 37}
{"curie": "MONDO:0002516", "names": ["GI tumor", "GI cancer", "gi cancer", "cancer gi", "GI CANCER", "cancers gi", "digestive cancer", "cancer digestive", "digestive cancers", "cancers digestive", "Neoplasm;digestive", "digestive neoplasm", "GI NEOPLASM MALIGNANT", "GI neoplasm malignant", "GASTROINTESTINAL CANCER", "digestive system cancer", "Gastrointestinal Cancer", "gastrointestinal cancer", "cancer gastrointestinal", "Cancer, Gastrointestinal", "Gastrointestinal Cancers", "gastrointestinal cancers", "digestive system neoplasm", "Digestive System Neoplasm", "Cancers, Gastrointestinal", "Malignant GI tract tumors", "Malignant GI tract tumours", "Digestive System Neoplasms", "Neoplasm, Digestive System", "cancer of digestive system", "Neoplasm of digestive tract", "Neoplasms, Digestive System", "Neoplasm of digestive system", "neoplasm of digestive system", "Gastrointestinal cancer, NOS", "gastrointestinal tract cancer", "Gastrointestinal Tract Cancer", "Gastrointestinal System Cancer", "malignant neoplasm of GI tract", "cancers gastrointestinal tract", "Gastrointestinal Tract Cancers", "gastrointestinal system cancer", "Gastrointestinal system--Cancer", "neoplasm of the digestive system", "Cancer of Gastrointestinal Tract", "Gastrointestinal tract cancer NOS", "gastrointestinal cancer (diagnosis)", "malignant gastrointestinal neoplasm", "Gastrointestinal neoplasm malignant", "Malignant Digestive System Neoplasm", "malignant digestive system neoplasm", "Malignant Gastrointestinal Neoplasm", "Cancer of the Gastrointestinal Tract", "Neoplasm of digestive tract (disorder)", "malignant neoplasm of digestive system", "Neoplasm of digestive system (disorder)", "Malignant gastrointestinal tract tumors", "Malignant gastrointestinal tract tumours", "neoplasm of digestive system (diagnosis)", "malignant tumor of gastrointestinal tract", "Malignant Gastrointestinal System Neoplasm", "malignant gastrointestinal system neoplasm", "malignant neoplasm of gastrointestinal tract", "Malignant neoplasm of gastrointestinal tract", "Malignant neoplasm of gastrointestinal tract NOS", "Malignant neoplasm of gastrointestinal tract, NOS", "Neoplasm of unspecified nature of digestive system", "Malignant neoplasm of gastrointestinal tract (disorder)", "malignant neoplasm of gastrointestinal tract (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "digestive system cancer", "shortest_name_length": 8}
{"curie": "UMLS:C5447477", "names": ["Advanced Malignant Genitourinary System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Malignant Genitourinary System Neoplasm", "shortest_name_length": 48}
{"curie": "UMLS:C5420433", "names": ["Benign Maxillofacial Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Maxillofacial Neoplasm", "shortest_name_length": 29}
{"curie": "MONDO:0019666", "names": ["BCYM4", "SEMD, Pakistani Type", "SEMD, PAKISTANI TYPE", "SEMD, Pakistani type", "spondylodysplasia and premature pubarche", "Spondylodysplasia And Premature Pubarche", "SPONDYLODYSPLASIA AND PREMATURE PUBARCHE", "Spondyloepimetaphyseal dysplasia PAPSS2 type", "spondyloepimetaphyseal dysplasia, PAPSS2 type", "Spondyloepimetaphyseal dysplasia, PAPSS2 type", "Spondyloepimetaphyseal dysplasia Pakistani type", "spondyloepimetaphyseal dysplasia Pakistani type", "Spondyloepimetaphyseal dysplasia, Pakistani type", "Spondyloepimetaphyseal Dysplasia, Pakistani Type", "spondyloepimetaphyseal dysplasia, Pakistani type", "SPONDYLOEPIMETAPHYSEAL DYSPLASIA, PAKISTANI TYPE", "brachyolmia 4 with mild epiphyseal and metaphyseal changes", "BRACHYOLMIA TYPE 4 WITH MILD EPIPHYSEAL AND METAPHYSEAL CHANGES", "brachyolmia type 4 with mild epiphyseal and metaphyseal changes", "Spondyloepimetaphyseal dysplasia 3-prime-phosphoadenosine 5-prime-phosphosulfate synthase 2 type", "Spondyloepimetaphyseal dysplasia PAPSS2 (3-prime-phosphoadenosine 5-prime-phosphosulfate synthase 2) type", "Spondyloepimetaphyseal dysplasia 3-prime-phosphoadenosine 5-prime-phosphosulfate synthase 2 type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepimetaphyseal dysplasia, PAPSS2 type", "shortest_name_length": 5}
{"curie": "MONDO:0004230", "names": ["adenomatoid tumor", "Adenomatoid tumor", "Adenomatoid Tumor", "Adenomatoid Tumors", "adenomatoid tumour", "adenomatoid tumors", "Tumor, Adenomatoid", "Adenomatoid tumour", "Benign Mesothelioma", "Tumors, Adenomatoid", "benign mesothelioma", "Benign mesothelioma", "Mesothelioma, Benign", "Mesothelioma, benign", "MESOTHELIOMA, BENIGN", "mesothelioma, benign", "Mesotheliomas benign", "Adenomatoid tumor NOS", "Adenomatoid tumour NOS", "Adenomatoid tumor, NOS", "Benign mesothelioma NOS", "Adenomatoid tumour, NOS", "Benign Mesothelial Tumor", "benign mesothelial tumor", "adenomatoid tumor, benign", "Adenomatoid Tumor, Benign", "benign mesothelial neoplasm", "Benign Mesothelial Neoplasm", "benign tumor of mesothelium", "Benign Tumor of Mesothelium", "benign neoplasm of mesothelium", "Benign Neoplasm of Mesothelium", "benign tumor of the mesothelium", "Benign Tumor of the Mesothelium", "Benign Neoplasm of the Mesothelium", "benign neoplasm of the mesothelium", "benign localised epithelial Mesothelioma", "benign localized epithelial Mesothelioma", "Benign Localized Epithelial Mesothelioma", "benign localized epithelial mesothelioma", "Adenomatoid tumor (morphologic abnormality)", "adenomatoid tumor (morphologic abnormality)", "Mesothelioma, benign (morphologic abnormality)", "adenomatoid tumor NOS (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenomatoid tumor", "shortest_name_length": 17}
{"curie": "MONDO:0016219", "names": ["Guizar Vasquez Sanchez Manzano syndrome", "Guízar Vázquez-Sánchez-Manzano syndrome", "dysmorphism-pectus carinatum-joint laxity syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dysmorphism-pectus carinatum-joint laxity syndrome", "shortest_name_length": 39}
{"curie": "MONDO:0000888", "names": ["mucositis", "Mucositis", "GI mucositis", "Gastrointestinal Mucositis", "Gastrointestinal mucositis", "gastrointestinal mucositis", "gastrointestinal system mucosaitis", "mucositis of gastrointestinal system", "Gastrointestinal mucositis (disorder)", "gastrointestinal system mucosa inflammation", "inflammation of gastrointestinal system mucosa", "mucositis of gastrointestinal system (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastrointestinal mucositis", "shortest_name_length": 9}
{"curie": "MONDO:0021220", "names": ["Eye Tumor", "eye tumor", "eye neoplasm", "Tumor of Eye", "Eye Neoplasm", "tumor of eye", "ocular tumor", "Ocular Tumor", "Ocular Neoplasm", "ocular neoplasm", "Neoplasm of Eye", "neoplasm of eye", "Tumor of the Eye", "tumor of the eye", "Neoplasm of the Eye", "neoplasm of the eye", "eye neoplasm (disease)", "eyeball of camera-type eye tumor", "eyeball of camera-type eye neoplasm", "tumor of eyeball of camera-type eye", "neoplasm of eyeball of camera-type eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eye neoplasm", "shortest_name_length": 9}
{"curie": "MONDO:0000209", "names": ["SMABF", "spinal muscular atrophy with congenital bone fractures", "prenatal-onset spinal muscular atrophy with congenital bone fractures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prenatal-onset spinal muscular atrophy with congenital bone fractures", "shortest_name_length": 5}
{"curie": "UMLS:C4744395", "names": ["Sellar Mixed Germ Cell Tumor", "Mixed Germ Cell Tumor of the Sellar Region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sellar Mixed Germ Cell Tumor", "shortest_name_length": 28}
{"curie": "OMIM:613418", "names": ["BMND15", "OSTEOPOROSIS, SUSCEPTIBILITY TO", "METAPHYSEAL FRACTURE, SUSCEPTIBILITY TO", "COMPRESSION FRACTURE, SUSCEPTIBILITY TO", "BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 15"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 6}
{"curie": "MONDO:0014946", "names": ["SIHIWES", "SIFRIM-HITZ-WEISS SYNDROME", "Sifrim-Hitz-Weiss syndrome", "Sifrim-Hitz-Weiss syndrome; SIHIWES", "SIFRIM-HITZ-WEISS MULTIPLE CONGENITAL ANOMALIES-MENTAL RETARDATION SYNDROME", "Sifrim-Hitz-Weiss multiple congenital anomalies-mental retardation syndrome", "Sifrim-Hitz-Weiss multiple congenital anomalies-intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sifrim-Hitz-Weiss syndrome", "shortest_name_length": 7}
{"curie": "MONDO:0100112", "names": ["ACBD5 deficiency", "acyl-CoA binding domain containing protein 5 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acyl-CoA binding domain containing protein 5 deficiency", "shortest_name_length": 16}
{"curie": "MONDO:0017320", "names": ["PEPCK deficiency", "Phosphopyruvate carboxylase deficiency", "Phosphoenolpyruvate carboxylase deficiency", "Phosphenolpyruvate carboxykinase deficiency", "Phosphoenolpyruvate carboxykinase deficiency", "Phosphoenolpyruvate Carboxykinase Deficiency", "phosphenolpyruvate carboxykinase; deficiency", "deficiency; phosphenolpyruvate carboxykinase", "phosphoenolpyruvate carboxykinase deficiency", "deficiency; phosphoenolpyruvate carboxykinase", "phosphoenolpyruvate carboxykinase; deficiency", "Deficiency of phosphoenolpyruvate carboxykinase", "phosphoenolpyruvate carboxykinase (GTP) deficiency", "Phosphoenolpyruvate carboxykinase (GTP) deficiency", "Phosphoenolpyruvate Carboxykinase (GTP) Deficiency", "PEPCK - Phosphenolpyruvate carboxykinase deficiency", "PEPCK - Phosphoenolpyruvate carboxykinase deficiency", "Phosphoenolpyruvate carboxykinase-1 (PCK1) deficiency", "Phosphoenolpyruvate carboxykinase deficiency (disorder)", "Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phosphoenolpyruvate carboxykinase deficiency", "shortest_name_length": 16}
{"curie": "MONDO:0020788", "names": ["HOMGSMR2", "HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION 2", "hypomagnesemia, seizures, and intellectual disability 2", "HYPOMAGNESEMIA, SEIZURES, AND IMPAIRED INTELLECTUAL DEVELOPMENT 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypomagnesemia, seizures, and intellectual disability 2", "shortest_name_length": 8}
{"curie": "MONDO:0012006", "names": ["Craniosynostosis with Ocular Abnormalities and Hallucal Defects", "CRANIOSYNOSTOSIS WITH OCULAR ABNORMALITIES AND HALLUCAL DEFECTS", "craniosynostosis with ocular abnormalities and hallucal defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniosynostosis with ocular abnormalities and hallucal defects", "shortest_name_length": 63}
{"curie": "MONDO:0012602", "names": ["DFNB24", "autosomal recessive deafness 24", "deafness, autosomal recessive 24", "DEAFNESS, AUTOSOMAL RECESSIVE 24", "Deafness, Autosomal Recessive, 24", "DEAFNESS, AUTOSOMAL RECESSIVE, 24", "deafness, autosomal recessive type 24", "autosomal recessive nonsyndromic deafness 24", "RDX autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 24", "autosomal recessive nonsyndromic deafness type 24", "autosomal recessive nonsyndromic deafness caused by mutation in RDX"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 24", "shortest_name_length": 6}
{"curie": "MONDO:0004490", "names": ["body of uterus gestational choriocarcinoma", "gestational uterine corpus choriocarcinoma", "gestational choriocarcinoma of body of uterus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gestational uterine corpus choriocarcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0004545", "names": ["Adult MPNST", "adult MPNST", "adult neurofibrosarcoma", "neurofibrosarcoma, adult", "neurogenic sarcoma, adult", "adult malignant schwannoma", "sarcoma, neurogenic, adult", "Adult Malignant Schwannoma", "malignant neurolemma, adult", "malignant schwannoma, adult", "sarcoma, neurofibro-, adult", "Adult Malignant Neurilemmoma", "schwannoma, malignant, adult", "adult malignant neurilemmoma", "neurolemma, malignant, adult", "Malignant Peripheral Nerve Sheath Tumor", "malignant peripheral nerve sheath tumor", "Adult Malignant Peripheral Nerve Sheath Tumor", "adult malignant peripheral nerve sheath tumor", "Adult Malignant Peripheral Nerve Sheath Neoplasm", "adult malignant tumor of peripheral nerve sheath", "adult malignant peripheral nerve sheath neoplasm", "Adult Malignant Tumor of Peripheral Nerve Sheath", "Adult Malignant Neoplasm of Peripheral Nerve Sheath", "adult malignant neoplasm of peripheral nerve sheath", "Adult Malignant Tumor of the Peripheral Nerve Sheath", "adult malignant tumor of the peripheral nerve sheath", "Adult Malignant Neoplasm of the Peripheral Nerve Sheath", "adult malignant neoplasm of the peripheral nerve sheath"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult malignant schwannoma", "shortest_name_length": 11}
{"curie": "UMLS:C1519218", "names": ["Secondary Prostate Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary Prostate Urothelial Carcinoma", "shortest_name_length": 39}
{"curie": "UMLS:C4524964", "names": ["stage IIA small intestine cancer", "Stage IIA Small Intestinal Adenocarcinoma", "stage IIA small intestinal adenocarcinoma AJCC v8", "Stage IIA Small Intestinal Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Small Intestinal Adenocarcinoma AJCC v8", "shortest_name_length": 32}
{"curie": "MONDO:0012188", "names": ["CLN9", "CLN 9", "CLN9 disease", "neuronal ceroid lipofuscinosis 9", "Ceroid lipofuscinosis, neuronal 9", "ceroid lipofuscinosis, neuronal, 9", "CEROID LIPOFUSCINOSIS, NEURONAL, 9", "Ceroid Lipofuscinosis, Neuronal, 9", "neuronal ceroid lipofuscinosis type 9", "CEROID LIPOFUSCINOSIS, NEURONAL, 9 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuronal ceroid lipofuscinosis 9", "shortest_name_length": 4}
{"curie": "UMLS:C5418992", "names": ["Unresectable Primary Central Chondrosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Primary Central Chondrosarcoma", "shortest_name_length": 43}
{"curie": "MONDO:0006995", "names": ["Tethered Cord", "tethered cord", "spinal dysraphism", "Spinal dysraphism", "Spinal cord syndrome", "spinal cord syndrome", "Spinal Cord Syndrome", "cord spinal syndrome", "cord spinal syndromes", "Spinal Cord Myelodysplasia", "spinal cord; myelodysplasia", "Myelodysplasia, Spinal Cord", "myelodysplasia; spinal cord", "Spinal Cord Myelodysplasias", "Myelodysplasias, Spinal Cord", "Tethered Spinal Cord Syndrome", "tethered spinal cord syndrome", "Myelodysplasia of spinal cord", "spinal cord syndrome (diagnosis)", "Myelodysplasia of the spinal cord", "Myelodysplasia of spinal cord (disorder)", "Structural developmental anomalies of neurenteric canal", "Structural developmental anomalies of neurenteric canal (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tethered spinal cord syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0019407", "names": ["SWILS", "Saul-Wilson syndrome", "SAUL-WILSON SYNDROME", "MICROCEPHALIC OSTEODYSPLASTIC DYSPLASIA", "microcephalic osteodysplastic dysplasia", "microcephalic osteodysplastic dysplasia, Saul-Wilson type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephalic osteodysplastic dysplasia, Saul-Wilson type", "shortest_name_length": 5}
{"curie": "MONDO:0100220", "names": ["RILDBC2", "RAJAB INTERSTITIAL LUNG DISEASE WITH BRAIN CALCIFICATIONS 2", "Rajab interstitial lung disease with brain calcifications 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rajab interstitial lung disease with brain calcifications 2", "shortest_name_length": 7}
{"curie": "MONDO:0014195", "names": ["MMCAT", "MMCAT syndrome", "microcornea-myopic chorioretinal atrophy", "microcornea, myopic chorioretinal atrophy, and telecanthus", "MICROCORNEA, MYOPIC CHORIORETINAL ATROPHY, AND TELECANTHUS", "microcornea-myopic chorioretinal atrophy-telecanthus syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcornea-myopic chorioretinal atrophy", "shortest_name_length": 5}
{"curie": "UMLS:C4683499", "names": ["Refractory Extensive Stage Small Cell Lung Carcinoma", "Refractory Extensive Stage Lung Small Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Extensive Stage Lung Small Cell Carcinoma", "shortest_name_length": 52}
{"curie": "MONDO:0033665", "names": ["DFNA78", "deafness, autosomal dominant 78", "DEAFNESS, AUTOSOMAL DOMINANT 78", "hearing loss, autosomal dominant 78", "autosomal dominant nonsyndromic deafness 78"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal dominant 78", "shortest_name_length": 6}
{"curie": "MONDO:0020698", "names": ["inborn error of biotin metabolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn error of biotin metabolism", "shortest_name_length": 33}
{"curie": "MONDO:0009457", "names": ["IMMUNOGLOBULIN D LEVEL IN PLASMA, LOW", "immunoglobulin d level in plasma, low", "IMMUNOGLOBULIN D level in plasma, LOW"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunoglobulin d level in plasma, low", "shortest_name_length": 37}
{"curie": "MONDO:0015029", "names": ["reticular perineurioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "reticular perineurioma", "shortest_name_length": 22}
{"curie": "MONDO:0012267", "names": ["HPE8", "Holoprosencephaly 8", "HOLOPROSENCEPHALY 8", "holoprosencephaly 8", "holoprosencephaly type 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "holoprosencephaly 8", "shortest_name_length": 4}
{"curie": "MONDO:0012159", "names": ["LNCR1", "lung cancer susceptibility", "lung cancer susceptibility 1", "LUNG CANCER SUSCEPTIBILITY 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung cancer susceptibility 1", "shortest_name_length": 5}
{"curie": "MONDO:0000298", "names": ["Dioctophymosis", "dioctophymosis", "dioctophymiasis", "Dioctophymiasis", "Dioctophymiases", "giant kidney worm disease", "Giant kidney worm disease", "Giant Kidney Worm Infection", "Dioctophyma renale infection", "Dioctophyma renale Infection", "dioctophyma renale infection", "Dioctophyme renale Infection", "Dioctophyme renale infection", "Infection, Dioctophyma renale", "Dioctophyme renale Infections", "Infection, Dioctophyme renale", "Dioctophyma renale Infections", "Dioctophyma renale; infection", "Infections, Dioctophyma renale", "Dioctophyma renale; infestation", "infestation; Dioctophyma renale", "Dioctophyme renale infectious disease", "Dioctophyme renale disease or disorder", "Dioctophyme renale infection (disorder)", "Dioctophyme renale caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dioctophymiasis", "shortest_name_length": 14}
{"curie": "MONDO:0030473", "names": ["DEE99", "early infantile epileptic encephalopathy 99", "developmental and epileptic encephalopathy 99", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 99"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy 99", "shortest_name_length": 5}
{"curie": "MONDO:0016195", "names": ["qualitative or quantitative defects of beta-myosin heavy chain (MYH7)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of beta-myosin heavy chain (MYH7)", "shortest_name_length": 69}
{"curie": "MONDO:0009963", "names": ["RL SYNDROME", "RL syndrome", "Ulbright-Hodes syndrome", "Ulbright Hodes syndrome", "renal dysplasia limb defects syndrome", "renal dysplasia-limb defects syndrome", "Renal Dysplasia-Limb Defects Syndrome", "Renal dysplasia-limb defects syndrome", "RENAL DYSPLASIA-LIMB DEFECTS SYNDROME", "Renal dysplasia - limb defects syndrome", "Renal dysplasia with limb defect syndrome", "Renal dysplasia, mesomelia, and radiohumeral fusion", "renal dysplasia, mesomelia, and radiohumeral fusion", "Renal dysplasia with limb defect syndrome (disorder)", "Renal dysplasia-mesomelia-radiohumeral fusion syndrome", "renal dysplasia-mesomelia-radiohumeral fusion syndrome", "Renal dysplasia, mesomelia, radiohumeral fusion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ulbright-Hodes syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0005025", "names": ["ENDOCARDITIS", "endocarditis", "Endocarditis", "Endocarditides", "ENDOCARDITIDES", "Endocarditis NOS", "Endocarditis, NOS", "Acute Endocarditis", "acute endocarditis", "endocarditis acute", "Endocarditis;acute", "Acute endocarditis", "acute; endocarditis", "Acute endocarditis NOS", "endocarditis (disease)", "Acute endocarditis, NOS", "Endocarditis (disorder)", "endocardium inflammation", "endocarditis (diagnosis)", "inflammation of endocardium", "Acute endocarditis (disorder)", "acute endocarditis (diagnosis)", "inflammation of the heart valve", "Acute endocarditis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endocarditis", "shortest_name_length": 12}
{"curie": "UMLS:C1336149", "names": ["Fallopian Tube Cancer Stage IC", "stage IC fallopian tube cancer", "fallopian tube cancer stage IC", "Stage IC Fallopian Tube Cancer", "AJCC Stage IC Fallopian Tube Cancer", "AJCC stage IC fallopian tube cancer", "Stage IC Fallopian Tube Cancer AJCC v7", "FIGO Stage IC Fallopian Tube Carcinoma", "FIGO stage IC fallopian tube carcinoma", "stage IC fallopian tube cancer AJCC v7", "stage IC fallopian tube cancer AJCC v6", "Stage IC Fallopian Tube Cancer AJCC v6", "FIGO Stage IC Carcinoma of Fallopian Tube", "FIGO stage IC carcinoma of fallopian fube", "FIGO Stage IC Carcinoma of the Fallopian Tube", "FIGO stage IC carcinoma of the fallopian tube", "Stage IC Fallopian Tube Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IC Fallopian Tube Cancer AJCC v6 and v7", "shortest_name_length": 30}
{"curie": "MONDO:0021355", "names": ["Esophagus Tumor", "esophageal mass", "Esophageal mass", "esophagus tumor", "esophagus tumors", "ESOPHAGEAL TUMOR", "Esophageal tumor", "esophageal tumor", "Esophageal Tumor", "esophageal masses", "esophageal tumors", "esophageal cancer", "Esophageal Tumors", "Esophageal tumour", "Esophagus--Tumors", "Tumor of esophagus", "Esophagus Neoplasm", "tumor of esophagus", "Tumor of Esophagus", "esophagus neoplasm", "Esophageal Neoplasm", "Esophagus Neoplasms", "Esophageal neoplasm", "esophageal neoplasm", "Neoplasm, Esophagus", "Esophageal Neoplasms", "Oesophageal neoplasm", "esophageal neoplasms", "Neoplasm, Esophageal", "Tumour of oesophagus", "Neoplasms, Esophagus", "Neoplasms, Esophageal", "Neoplasm of esophagus", "Neoplasm of Esophagus", "neoplasm of esophagus", "Neoplasm of oesophagus", "tumor of the esophagus", "Tumor of the Esophagus", "Esophageal neoplasm NOS", "Oesophageal neoplasm NOS", "Neoplasm of the Esophagus", "neoplasm of the esophagus", "esophageal tumor or cancer", "esophagus neoplasm (disease)", "Neoplasm of esophagus (disorder)", "neoplasm of esophagus (diagnosis)", "esophageal neoplasms, benign and malignant", "Esophageal Neoplasms, Benign and Malignant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplasm of esophagus", "shortest_name_length": 15}
{"curie": "MONDO:0014795", "names": ["RREI", "exercise intolerance, riboflavin-responsive", "EXERCISE INTOLERANCE, RIBOFLAVIN-RESPONSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exercise intolerance, riboflavin-responsive", "shortest_name_length": 4}
{"curie": "UMLS:C0852976", "names": ["Retro-Orbital Tumor", "Retro-Orbital Neoplasm", "Retro-orbital neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retro-orbital neoplasm", "shortest_name_length": 19}
{"curie": "MONDO:0001700", "names": ["IGS", "RH-MGA1", "MEGALOBLASTIC", "megaloblastic", "MGA1 Norwegian type", "MEGALOBLASTIC ANEMIA", "Anemia megaloblastic", "Megaloblastic Anemia", "Megaloblastic anemia", "ANEMIA MEGALOBLASTIC", "anemia megaloblastic", "megaloblastic anemia", "megaloblastic anemias", "Anaemia megaloblastic", "anemia; megaloblastic", "Megaloblastic Anemias", "Megaloblastic anaemia", "ANAEMIA MEGALOBLASTIC", "Anemia, Megaloblastic", "megaloblastic; anemia", "Anaemia;megaloblastic", "megaloblastic anaemia", "Anemias, Megaloblastic", "Megaloblastic anemia NOS", "Megaloblastic anaemia NOS", "Megaloblastic anemia, NOS", "Megaloblastic anaemia, NOS", "Imerslund-Grasbeck syndrome", "Grasbeck-Imerslund syndrome", "megaloblastic anemia (disease)", "Megaloblastic anemia (disorder)", "megaloblastic anemia (diagnosis)", "recessive hereditary megaloblastic anemia 1", "recessive hereditary megaloblastic anaemia 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "megaloblastic anemia", "shortest_name_length": 3}
{"curie": "MONDO:0005561", "names": ["aorta disease", "Aorta Disease", "aorta disorder", "aortic disease", "aorta diseases", "Aortic Disease", "Aortic disorder", "Aortic Diseases", "aortic disorder", "Disease, Aortic", "Aorta--Diseases", "aortic diseases", "disease of aorta", "Diseases, Aortic", "aortic disorders", "disorder of aorta", "Disorder of aorta", "Disease of the aorta", "disorder of the aorta", "diseases of the aorta", "DISEASES OF THE AORTA", "Disorder of aorta, NOS", "Disease of the aorta, NOS", "aorta disease or disorder", "Disorder of aorta (disorder)", "disease or disorder of aorta", "disorder of aorta (diagnosis)", "vascular system disorders disorder of aorta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic disorder", "shortest_name_length": 13}
{"curie": "UMLS:C4331921", "names": ["Obesity-Associated Insulin Resistance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Obesity-Associated Insulin Resistance", "shortest_name_length": 37}
{"curie": "UMLS:C4525089", "names": ["Stage IIC Colorectal Cancer AJCC v8", "Stage IIC Colorectal Carcinoma AJCC v8", "Stage IIC Colorectal (Colon or Rectal) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIC Colorectal Cancer AJCC v8", "shortest_name_length": 35}
{"curie": "UMLS:C0161558", "names": ["BARBITURATE", "barbiturate", "barbiturate toxicity", "Barbiturate Poisoning", "barbiturate poisoning", "Barbiturate poisoning", "Poisoning by barbiturate", "BARBITURATE INTOXICATION", "barbiturate intoxication", "Barbiturate intoxication", "Barbiturate Intoxication", "Poisoning by barbiturates", "Poisoning by barbiturate, NOS", "Poisoning by barbiturates NOS", "Barbiturate intoxication (NOS)", "BARBITURATE INTOXICATION (NOS)", "Poisoning caused by barbiturate", "barbiturate toxicity (diagnosis)", "Poisoning caused by barbiturate (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Poisoning by barbiturate", "shortest_name_length": 11}
{"curie": "MONDO:0005345", "names": ["HYPOSPADIA", "hypospadia", "Hypospadia", "hypospadias", "Hypospadias", "HYPOSPADIAS", "Hypospadia;M", "Hypospadias,", "penis hypospadias", "familial hypospadias", "hypospadias familial", "hypospadias (disease)", "congenital hypospadia", "Hypospadias (disorder)", "Hypospadia;congenital;M", "Hypospadias, unspecified", "hypospadias (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypospadias", "shortest_name_length": 10}
{"curie": "MONDO:0030961", "names": ["PPKM2", "OLMS2", "OLMSTED SYNDROME 2", "Olmsted syndrome 2", "palmoplantar keratoderma, mutilating, with periorificial keratotic plaques 2", "PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTIC PLAQUES 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Olmsted syndrome 2", "shortest_name_length": 5}
{"curie": "MONDO:0004469", "names": ["pseudovascular skin squamous cell carcinoma", "Pseudovascular Skin Squamous Cell Carcinoma", "skin pseudovascular squamous cell carcinoma", "Skin Pseudovascular Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudovascular skin squamous cell carcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0021541", "names": ["Retina Angioma", "retina angioma", "Retinal angioma", "Retinal Angioma", "retinal angioma", "retina hemangioma", "Retinal angiomata", "Retina Hemangioma", "angioma of retina", "Retinal Hemangioma", "retinal hemangioma", "Retinal hemangioma", "Retinal haemangioma", "hemangioma of retina", "Hemangioma of retina", "angioma of the retina", "Haemangioma of retina", "hemangioma of the retina", "Hemangioma of retina (disorder)", "hemangioma of retina (diagnosis)", "angioma of retina (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemangioma of retina", "shortest_name_length": 14}
{"curie": "UMLS:C5205930", "names": ["Prostate Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Diffuse Large B-Cell Lymphoma", "shortest_name_length": 38}
{"curie": "MONDO:0018521", "names": ["pancreas squamous cell carcinoma", "Pancreatic squamous cell carcinoma", "Pancreatic Squamous Cell Carcinoma", "pancreatic squamous cell carcinoma", "squamous cell carcinoma of pancreas", "Squamous cell carcinoma of pancreas", "Squamous cell carcinoma of the pancreas", "squamous cell carcinoma of the pancreas", "squamous cell carcinoma of pancreas (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "squamous cell carcinoma of pancreas", "shortest_name_length": 32}
{"curie": "UMLS:C0151785", "names": ["mucosa disease", "membrane mucous", "Mucosal disease", "MUCOUS MEMBRANE", "mucosal disease", "Mucosal disorder", "diseases mucosal", "Disease of mucosa", "Mucosal disease, NOS", "Disease of mucosa, NOS", "Mucous membrane disorder", "MUCOUS MEMBRANE DISORDER", "disorders membrane mucous", "Disease of mucous membrane", "Disorder of mucous membrane", "Mucous membrane disorder NOS", "Mucous membrane disorder, NOS", "MUCOUS MEMBRANE DISORDER (NOS)", "Membrane mucous disorder (NOS)", "MEMBRANE MUCOUS DISORDER (NOS)", "Disease of mucous membrane, NOS", "DISEASES OF THE MUCOUS MEMBRANES", "Disorder of mucous membrane (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disease of mucous membrane", "shortest_name_length": 14}
{"curie": "MONDO:0000726", "names": ["scoliosis idiopathic", "Idiopathic scoliosis", "idiopathic scoliosis", "Scoliosis, idiopathic", "idiopathic; scoliosis", "scoliosis; idiopathic", "Idiopathic scoliosis (disorder)", "idiopathic scoliosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic scoliosis", "shortest_name_length": 20}
{"curie": "UMLS:C3888734", "names": ["Medical device site pain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Medical device site pain", "shortest_name_length": 24}
{"curie": "MONDO:0043465", "names": ["achylia", "ACHLORHYDRIA", "Achlorhydria", "achlorhydria", "hypochlorhydria", "achylia gastrica", "Achylia Gastrica", "Achylia gastrica", "ACHYLIA GASTRICA", "Gastric anacidity", "gastric anacidity", "Anacidity, gastric", "gastric achlorhydria", "Achlorhydria, gastric", "absent gastric acidity", "Absent gastric acidity", "Achlorhydria (disorder)", "Gastric acidity, absent", "achlorhydria (diagnosis)", "Achylia gastrica (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "achlorhydria", "shortest_name_length": 7}
{"curie": "MONDO:0008100", "names": ["invert nipple", "invert nipples", "Indrawn nipple", "inverted nipple", "Inverted nipple", "nipple inverted", "NIPPLE INVERTED", "INVERTED NIPPLE", "nipple inversion", "NIPPLES INVERTED", "Inverted nipples", "inverted nipples", "nipples inverted", "inversion; nipple", "nipple; inversion", "Invaginated nipples", "inversion of nipple", "Inversion of nipple", "Mammillae Invertitae", "MAMMILLAE INVERTITAE", "inversion of nipple (symptom)", "Inversion of nipple (disorder)", "breast appearance nipple inversion", "inversion of nipple (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nipples inverted", "shortest_name_length": 13}
{"curie": "UMLS:C4543165", "names": ["Acute myeloid leukemia with FTL3 mutation", "Acute myeloid leukaemia with FTL3 mutation", "Acute myeloid leukemia with FMS-like tyrosine kinase-3 mutation", "Acute myeloid leukaemia with FMS-like tyrosine kinase-3 mutation", "Acute myeloid leukemia with FMS-like tyrosine kinase-3 mutation (disorder)", "Acute myeloid leukemia with FMS-like tyrosine kinase-3 mutation (diagnosis)", "Acute myeloid leukemia with FMS-like tyrosine kinase-3 mutation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute myeloid leukemia with FMS-like tyrosine kinase-3 mutation", "shortest_name_length": 41}
{"curie": "MONDO:0001337", "names": ["seborrheic keratosis inflamed", "inflamed seborrheic keratosis", "Inflamed seborrheic keratosis", "Inflamed seborrhoeic keratosis", "Inflamed seborrheic keratosis (disorder)", "inflamed seborrheic keratosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflamed seborrheic keratosis", "shortest_name_length": 29}
{"curie": "UMLS:C2987497", "names": ["Stage IV Bladder Cancer", "Stage IV Bladder Carcinoma", "Stage IV Bladder Cancer AJCC v7", "Stage IV Bladder Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Bladder Cancer AJCC v7", "shortest_name_length": 23}
{"curie": "MONDO:0700161", "names": ["Canine Gastrointestinal Stromal Tumor", "canine gastrointestinal stromal tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canine gastrointestinal stromal tumor", "shortest_name_length": 37}
{"curie": "MONDO:0019952", "names": ["myopathy congenital", "congenital myopathy", "Batten Turner congenital myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myopathy", "shortest_name_length": 19}
{"curie": "UMLS:C1266088", "names": ["Carcinoma with neuroendocrine differentiation", "Adenocarcinoma with Neuroendocrine Differentiation", "adenocarcinoma with neuroendocrine differentiation", "Adenocarcinoma with neuroendocrine differentiation", "adenocarcinoma with neuroendocrine differentiation (diagnosis)", "Adenocarcinoma with neuroendocrine differentiation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma with neuroendocrine differentiation", "shortest_name_length": 45}
{"curie": "MONDO:0013582", "names": ["MVA2", "Mosaic Variegated Aneuploidy Syndrome 2", "MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2", "MOSAIC variegated aneuploidy syndrome 2", "mosaic variegated aneuploidy syndrome 2", "CEP57 mosaic variegated aneuploidy syndrome", "mosaic variegated aneuploidy syndrome type 2", "Mosaic variegated aneuploidy syndrome type 2", "mosaic variegated aneuploidy syndrome caused by mutation in CEP57"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mosaic variegated aneuploidy syndrome 2", "shortest_name_length": 4}
{"curie": "UMLS:C0751864", "names": ["MPTP Induced Degeneration of the Striatum", "MPTP-Induced Degeneration of the Striatum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MPTP-Induced Degeneration of the Striatum", "shortest_name_length": 41}
{"curie": "MONDO:0002492", "names": ["arf", "ARF", "AKI", "Acute Renal Injury", "kidney injury acute", "Acute Kidney Injury", "RENAL FAILURE ACUTE", "Renal Injury, Acute", "ACUTE RENAL FAILURE", "acute renal failure", "Acute Renal Failure", "Failure;renal;acute", "Renal failure acute", "Acute kidney injury", "acute kidney injury", "Acute renal failure", "renal failure acute", "acute failure renal", "failure acute renal", "KIDNEY FAILURE ACUTE", "Failure kidney acute", "Acute Kidney Failure", "acute failure kidney", "RENAL FAILURE, ACUTE", "acute kidney failure", "Kidney failure acute", "Acute kidney failure", "FAILURE KIDNEY ACUTE", "Kidney Injury, Acute", "acute renal shutdown", "acute renal failures", "Acute Renal Injuries", "kidney failure acute", "Renal Failure, Acute", "Acute Renal Failures", "ACUTE KIDNEY FAILURE", "Renal shutdown acute", "RENAL SHUTDOWN ACUTE", "Renal Injuries, Acute", "Acute Kidney Injuries", "Kidney Failure, Acute", "Renal Failures, Acute", "kidney failure, acute", "Acute Kidney Failures", "KIDNEY, FAILURE, ACUTE", "Acute injury of kidney", "Kidney Failures, Acute", "Kidney Injuries, Acute", "ARF (acute renal failure)", "acute renal insufficiency", "AKI - acute kidney injury", "ARF - Acute renal failure", "Renal insufficiency, acute", "syndrome acute renal failure", "Acute renal failure syndrome", "acute renal failure (diagnosis)", "Acute kidney injury (diagnosis)", "Acute renal failure, unspecified", "Acute renal failure syndrome, NOS", "Acute injury of kidney (disorder)", "Acute kidney failure, unspecified", "Acute and unspecified renal failure", "Acute renal failure syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute kidney failure", "shortest_name_length": 3}
{"curie": "UMLS:C1335042", "names": ["Non-Neoplastic Skin Disorder", "Non-Neoplastic Cutaneous Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Skin Disorder", "shortest_name_length": 28}
{"curie": "UMLS:C1518745", "names": ["Ovarian Trabecular Carcinoid Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Trabecular Carcinoid Tumor", "shortest_name_length": 34}
{"curie": "MONDO:0043110", "names": ["jones hersh yusk syndrome", "Jones Hersh Yusk syndrome", "Aplasia cutis cleft palate epidermolysis", "aplasia cutis cleft palate epidermolysis", "ptosis, ectropion, thin skin, beaked nose", "Ptosis, ectropion, thin skin, beaked nose", "aplasia cutis congenita, cleft palate, epidermolysis bullosa, and ectrodactyly", "Aplasia cutis congenita, cleft palate, epidermolysis bullosa, and ectrodactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "jones hersh yusk syndrome", "shortest_name_length": 25}
{"curie": "UMLS:C1332497", "names": ["Benign Extrahepatic Bile Duct Soft Tissue Tumor", "Benign Soft Tissue Tumor of Extrahepatic Bile Duct", "Benign Extrahepatic Bile Duct Soft Tissue Neoplasm", "Benign Soft Tissue Neoplasm of Extrahepatic Bile Duct", "Benign Soft Tissue Tumor of the Extrahepatic Bile Duct", "Benign Soft Tissue Neoplasm of the Extrahepatic Bile Duct"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Extrahepatic Bile Duct Soft Tissue Neoplasm", "shortest_name_length": 47}
{"curie": "MONDO:0019692", "names": ["multiple epiphyseal dysplasia and pseudoachondroplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple epiphyseal dysplasia and pseudoachondroplasia", "shortest_name_length": 54}
{"curie": "UMLS:C5420148", "names": ["Refractory Lung Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Lung Squamous Cell Carcinoma", "shortest_name_length": 39}
{"curie": "UMLS:C3274485", "names": ["Congenital Vena Cava Abnormality", "Congenital Abnormality of Vena Cava"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Vena Cava Abnormality", "shortest_name_length": 32}
{"curie": "MONDO:0022535", "names": ["carotodynia", "carotidynia", "CAROTODYNIA", "Carotodynia", "Carotidynia", "Carotidynia (disorder)", "CAROTID ARTERY TENDERNESS", "Autonomic facial cephalgia", "autonomic facial cephalgia", "tenderness of carotid artery", "Autonomic facial cephalgia (disorder)", "tenderness of carotid artery (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autonomic facial cephalgia", "shortest_name_length": 11}
{"curie": "MONDO:0005098", "names": ["CVA", "STROKE", "stroke", "Stroke", "strokes", "CVA NOS", "Strokes", "Apoplexy", "CVA, NOS", "APOPLEXY", "apoplexy", "Stroke NOS", "Stroke/CVA", "Stroke, NOS", "Brain Attack", "Brain attack", "Apoplexy, NOS", "stroke syndrome", "stroke disorder", "Stroke Syndrome", "stroke cerebral", "Cerebral Stroke", "cerebral stroke", "Stroke, Cerebral", "apoplexy; stroke", "Cerebral Strokes", "syndrome, stroke", "Stroke (Cerebrum)", "Strokes, Cerebral", "cerebral; apoplexy", "cerebral; accident", "stroke; apoplectic", "APOPLEXY, CEREBRAL", "accident; cerebral", "apoplexy; cerebral", "Cerebral Infarction", "UNDETERMINED STROKE", "cerebral infarction", "undetermined stroke", "Stroke, neurological", "cerebrovascular stroke", "Cerebral apoplexy, NOS", "Cerebrovascular Stroke", "Brain Vascular Accident", "vascular brain accident", "Stroke, cerebrovascular", "Cerebrovascular Strokes", "Stroke, Cerebrovascular", "Cerebrovascular Apoplexy", "Brain Vascular Accidents", "Cerebrovascular Accident", "Cerebrovascular accident", "cerebrovascular accident", "CEREBROVASCULAR ACCIDENT", "ACCIDENT CEREBROVASCULAR", "Accident cerebrovascular", "Vascular Accident, Brain", "Cerebral vascular events", "Strokes, Cerebrovascular", "Apoplexy, Cerebrovascular", "cerebrovascular accidents", "Vascular Accidents, Brain", "accident; cerebrovascular", "Cerebrovascular Accidents", "cerebrovascular; accident", "Cerebrovascular accidents", "Cerebral vascular accident", "vascular cerebral accident", "CEREBRAL VASCULAR ACCIDENT", "cerebral vascular accident", "Cerebrovascular accident NOS", "CVA, cerebrovascular accident", "Cerebrovascular accident, NOS", "CVA - Cerebrovascular accident", "CVA (Cerebrovascular Accident)", "cerebrovascular accident, (CVA)", "CVAs (Cerebrovascular Accident)", "Stroke/cerebrovascular accident", "CVA (cerebral vascular accident)", "Cerebrovascular accident (disorder)", "Stroke, not specified as hemorrhage or infarction", "Stroke, not specified as haemorrhage or infarction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stroke disorder", "shortest_name_length": 3}
{"curie": "UMLS:C2828188", "names": ["Stage III Gestational Trophoblastic Tumor", "stage III gestational trophoblastic tumor", "stage III gestational trophoblastic tumor AJCC v7", "Stage III Gestational Trophoblastic Tumor AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Gestational Trophoblastic Tumor AJCC v7", "shortest_name_length": 41}
{"curie": "UMLS:C0432485", "names": ["Transplant disorder", "Transplant Complication", "complications transplant", "Complication of transplant", "complication of transplant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Complication of transplant", "shortest_name_length": 19}
{"curie": "MONDO:0017601", "names": ["DLBCL with chronic inflammation", "diffuse large B-cell lymphoma with chronic inflammation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diffuse large B-cell lymphoma with chronic inflammation", "shortest_name_length": 31}
{"curie": "MONDO:0009784", "names": ["OPHTHALMOPLEGIC NEUROMUSCULAR DISORDER WITH ABNORMAL MITOCHONDRIA", "Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria", "ophthalmoplegic neuromuscular disorder with abnormal mitochondria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ophthalmoplegic neuromuscular disorder with abnormal mitochondria", "shortest_name_length": 65}
{"curie": "UMLS:C3854374", "names": ["Transplantation associated food allergy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transplantation associated food allergy", "shortest_name_length": 39}
{"curie": "UMLS:C2242583", "names": ["Acute liver injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute liver injury", "shortest_name_length": 18}
{"curie": "MONDO:0009795", "names": ["OFD9", "Ofds 9", "OFDS IX", "OFD syndrome 9", "orofaciodigital syndrome 9", "Orofaciodigital syndrome 9", "orofaciodigital syndrome IX", "OROFACIODIGITAL SYNDROME IX", "Orofaciodigital syndrome IX", "digito-orofacial syndrome IX", "Oral-facial-digital syndrome 9", "oral facial digital syndrome 9", "orofaciodigital syndrome type 9", "oral-facial-digital syndrome IX", "Orofaciodigital syndrome type 9", "Orofaciodigital Syndrome, Type 9", "orofaciodigital syndrome type IX", "orofaciodigital (OFD) syndrome IX", "Oro-facial digital syndrome type 9", "oral-facial-digital syndrome type 9", "Oral-facial-digital syndrome type 9", "oral facial digital syndrome type 9", "oral-Facial-digital syndrome, type 9", "ORAL-FACIAL-DIGITAL SYNDROME, TYPE IX", "Oral Facial Digital Syndrome, Type IX", "Oro-facial digital syndrome type 9 (disorder)", "oral-facial-digital syndrome type 9 (diagnosis)", "Orofaciodigital syndrome with retinal abnormality", "OROFACIODIGITAL SYNDROME WITH RETINAL ABNORMALITIES", "Orofaciodigital syndrome with retinal abnormalities", "orofaciodigital syndrome with retinal abnormalities", "ORAL-FACIAL-DIGITAL SYNDROME WITH RETINAL ABNORMALITIES", "Oral-facial-digital syndrome with retinal abnormalities", "oral-Facial-digital syndrome with retinal abnormalities", "oral-facial-digital syndrome with retinal abnormalities", "oral-facial-digital (OFD) syndrome with retinal abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orofaciodigital syndrome IX", "shortest_name_length": 4}
{"curie": "MONDO:0017449", "names": ["split hand", "split hand (disease)", "ectrodactyly of hand"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "split hand", "shortest_name_length": 10}
{"curie": "MONDO:0002242", "names": ["clotting factor deficiency", "Deficiency;clotting factor", "coagulation protein disease", "clotting factor; deficiency", "Coagulation factor disorder", "deficiency; clotting factor", "Coagulation factor decreased", "clotting deficiencies factor", "COAGULATION FACTOR DECREASED", "Coagulation Protein Disorder", "Decreased coagulation factors", "Coagulation Proteins Disorder", "Protein Disorder, Coagulation", "Disorder, Coagulation Protein", "Coagulation factor deficiency", "Coagulation factors decreased", "Coagulation Factor Deficiency", "coagulation factor deficiency", "Coagulation Protein Disorders", "coagulation deficiency factors", "Disorders, Coagulation Protein", "Proteins Disorder, Coagulation", "Disorder, Coagulation Proteins", "Coagulation Proteins Disorders", "Protein Disorders, Coagulation", "Coagulation factor deficiencies", "Disorders, Coagulation Proteins", "Proteins Disorders, Coagulation", "Coagulation factor disorder, NOS", "Deficiency of coagulation factors", "Deficiency, coagulation factor NOS", "Blood Coagulation Factor Deficiencies", "congenital clotting factor deficiency", "coagulation factor deficiency syndrome", "Coagulation factor deficiency syndrome", "Coagulation Factor Deficiency Syndrome", "COAGULATION FACTOR DEFICIENCY SYNDROMES", "Blood clotting factor deficiency disorder", "Coagulation factor deficiency syndrome, NOS", "Blood clotting factor deficiency disorder, NOS", "congenital clotting factor deficiency (diagnosis)", "Coagulation factor deficiency syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coagulation protein disease", "shortest_name_length": 26}
{"curie": "UMLS:C0032300", "names": ["Lobar Pneumonia", "Pneumonia lobar", "PNEUMONIA LOBAR", "Pneumonia;lobar", "lobar pneumonia", "Lobar pneumonia", "lobar; pneumonia", "PNEUMONIA, LOBAR", "Pneumonia, lobar", "Pneumonia, Lobar", "pneumonia; lobar", "Lobar Pneumonias", "Pneumonias, Lobar", "Lobar pneumonia NOS", "pneumonia pneumococcal", "pneumococcal pneumonia", "Lobar pneumonia (disorder)", "lobar pneumonia (diagnosis)", "Lobar pneumonia, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lobar Pneumonia", "shortest_name_length": 15}
{"curie": "UMLS:C0740343", "names": ["Mononeuropathy multiplex", "mononeuropathy multiplex", "Mononeuropathy Multiplex", "Mononeuropathy Multiplex Syndrome", "Mononeuropathy multiplex syndrome", "Mononeuropathy Multiplex Syndromes", "Syndrome, Mononeuropathy Multiplex", "Syndromes, Mononeuropathy Multiplex"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mononeuropathy Multiplex", "shortest_name_length": 24}
{"curie": "MONDO:0009778", "names": ["OPCA II, Fickler-Winkler Type", "OPCA II, FICKLER-WINKLER TYPE", "OPCA II, Fickler-Winkler type", "CEREBELLAR ATAXIA AND ALBINISM", "Olivopontocerebellar Atrophy II, Autosomal Recessive", "OLIVOPONTOCEREBELLAR ATAXIA II, FICKLER-WINKLER TYPE", "olivopontocerebellar atrophy II, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "olivopontocerebellar atrophy II, autosomal recessive", "shortest_name_length": 29}
{"curie": "MONDO:0005919", "names": ["insufficiency placental", "placental insufficiency", "Placental Insufficiency", "Placental insufficiency", "insufficiency; placental", "insufficiency, placental", "placental; insufficiency", "Insufficiency, Placental", "Placental insufficiency syndrome", "placental; insufficiency syndrome", "placental disorders insufficiency", "Placental insufficiency (disorder)", "insufficiency; placental, syndrome", "Chronic fetal deprivation syndrome", "placental insufficiency (diagnosis)", "Uteroplacental vascular insufficiency", "uteroplacental vascular insufficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "placental insufficiency", "shortest_name_length": 23}
{"curie": "MONDO:0011156", "names": ["PFIC2", "BSEP deficiency", "severe ABCB11 deficiency", "BSEP (bile salt export pump) deficiency", "progressive familial intrahepatic cholestasis 2", "Progressive familial intrahepatic cholestasis 2", "Cholestasis, progressive familial intrahepatic 2", "cholestasis, progressive familial intrahepatic 2", "CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 2", "cholestasis, progressive familial intrahepatic, 2", "Cholestasis, Progressive Familial Intrahepatic, 2", "Progressive familial intrahepatic cholestasis type 2", "ABCB11 progressive familial intrahepatic cholestasis", "progressive familial intrahepatic cholestasis type 2", "cholestasis, progressive familial intrahepatic, type 2", "PFIC2 Progressive familial intrahepatic cholestasis type 2", "PFIC2 - progressive familial intrahepatic cholestasis type 2", "Progressive familial intrahepatic cholestasis type 2 (disorder)", "progressive familial intrahepatic cholestasis type 2 (diagnosis)", "progressive familial intrahepatic cholestasis caused by mutation in ABCB11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive familial intrahepatic cholestasis type 2", "shortest_name_length": 5}
{"curie": "UMLS:C0278471", "names": ["stage II adult HD", "adult HD, stage II", "HD, adult, stage II", "HD, stage II, adult", "Stage II Hodgkin Lymphoma", "Stage II Adult Hodgkin Lymphoma", "stage II adult Hodgkin lymphoma", "Adult Hodgkin's Disease Stage II", "Stage II Adult Hodgkin's Disease", "stage II adult Hodgkin's disease", "adult Hodgkin's disease, stage II", "Adult Hodgkin's Lymphoma Stage II", "Stage II Adult Hodgkin's Lymphoma", "lymphoma, stage II adult Hodgkin's", "Hodgkin's disease, stage II, adult", "Hodgkin's lymphoma, stage II, adult", "Ann Arbor Stage II Adult Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Adult Hodgkin Lymphoma", "shortest_name_length": 17}
{"curie": "MONDO:0000479", "names": ["segmental dystonia", "Segmental dystonia", "Segmental dystonia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "segmental dystonia", "shortest_name_length": 18}
{"curie": "UMLS:C4331270", "names": ["Salt-wasting 21-OHD", "Salt-Wasting 21-Hydroxylase Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Salt-Wasting 21-Hydroxylase Deficiency", "shortest_name_length": 19}
{"curie": "MONDO:0013600", "names": ["DSPD", "DSPS", "insomnia", "INSOMNIA", "Insomnia", "Insomnias", "Insomnia NOS", "Insomnia, NOS", "Sleeplessness", "sleeplessness", "SLEEPLESSNESS", "Fragmented sleep", "Insomnia Disorder", "insomnia disorder", "Insomnia disorder", "Insomnia Disorders", "insomnia (disease)", "insomnia (symptom)", "Insomnia (disorder)", "Insomnia, unspecified", "sleep disorder insomnia", "SLEEP DISORDER INSOMNIA", "insomnia disorder (diagnosis)", "Disturbances of sleep/insomnia", "Difficulty staying or falling asleep", "Sleep Initiation and Maintenance Disorders", "disorders of initiating or maintaining sleep", "disorder of initiating and maintaining sleep", "Disorders of Initiating and Maintaining Sleep", "Disorders of initiating and maintaining sleep", "delayed sleep phase syndrome, susceptibility to", "delayed sleep phase disorder, susceptibility to", "sleep disorder; initiating or maintaining sleep", "initiating or maintaining sleep; sleep disorder", "DIMS (Disorders of Initiating and Maintaining Sleep)", "Disorders of initiating and maintaining sleep (disorder)", "disorder of initiating and maintaining sleep (diagnosis)", "Disorders of initiating and maintaining sleep [insomnias]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "insomnia", "shortest_name_length": 4}
{"curie": "UMLS:C1334170", "names": ["indolent lymphoma", "NHL, indolent, NOS", "Indolent Non-Hodgkin Lymphoma", "Indolent non-Hodgkin lymphoma", "Indolent Non-Hodgkin's Lymphoma", "Non-Hodgkin lymphoma, indolent, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Indolent Non-Hodgkin Lymphoma", "shortest_name_length": 17}
{"curie": "MONDO:0005972", "names": ["Lobar pneumonia", "Pneumonia pneumococcal", "Pneumococcal pneumonia", "pneumococcal pneumonia", "PNEUMOCOCCAL PNEUMONIA", "Pneumococcal Pneumonia", "PNEUMONIA PNEUMOCOCCAL", "pneumonia streptococcal", "streptococcal pneumonia", "Pneumonia streptococcal", "Streptococcal pneumonia", "Streptococcus pneumonia", "Pneumonia, Pneumococcal", "pneumonia; pneumococcus", "pneumococcus; pneumonia", "PNEUMONIA, PNEUMOCOCCAL", "Streptococcal Pneumonia", "Pneumococcal Pneumonias", "Pneumonias, Pneumococcal", "streptoccocal; pneumonia", "PNEUMONIA, STREPTOCOCCAL", "pneumonia; streptoccocal", "streptococcal; pneumoniae", "pneumoniae; streptoccocal", "Pneumonia due to Streptococcus", "pneumonia due to streptococcus", "pneumonia caused by streptococcus", "Pneumonia caused by Streptococcus", "Pneumococcal pneumonia (disorder)", "Streptococcus pneumoniae pneumonia", "PNEUMONIA, HEMOLYTIC STREPTOCOCCAL", "pneumococcal pneumonia (diagnosis)", "pneumonia; Streptococcus pneumoniae", "streptococcal pneumonia (diagnosis)", "Streptococcus; pneumoniae, pneumonia", "pneumonia due to Streptococcus pneumoniae", "Pneumonia due to Streptococcus pneumoniae", "Streptococcus pneumoniae caused pneumonia", "Pneumonia due to unspecified Streptococcus", "Pneumonia due to Streptococcus, unspecified", "Pneumonia caused by Streptococcus (disorder)", "streptoccocal; pneumonia, Streptococcus pneumoniae", "Pneumococcal pneumonia [Streptococcus pneumoniae pneumonia]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "streptococcal pneumonia", "shortest_name_length": 15}
{"curie": "UMLS:C4724451", "names": ["Recurrent T Acute Lymphoblastic Leukemia", "Recurrent T-Acute Lymphoblastic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent T Acute Lymphoblastic Leukemia", "shortest_name_length": 40}
{"curie": "MONDO:0002966", "names": ["spleen prolymphocytic leukemia", "prolymphocytic leukemia of spleen", "splenic manifestation of prolymphocytic leukemia", "Splenic Manifestation of Prolymphocytic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "splenic manifestation of prolymphocytic leukemia", "shortest_name_length": 30}
{"curie": "UMLS:C0347003", "names": ["Metastasis to testis", "Metastases to testicle", "Metastatic tumor to testis", "Metastatic tumour to testis", "Metastatic Tumor to the Testis", "Metastatic Neoplasm to the Testis", "Secondary malignant neoplasm of testis", "Metastatic malignant neoplasm to testis", "Metastatic malignant neoplasm of testis", "Metastatic Malignant Neoplasm to the Testis", "Secondary malignant neoplasm of testis, NOS", "Metastatic Malignant Neoplasm in the Testis", "Metastatic malignant neoplasm to testis, NOS", "Metastatic malignant neoplasm to testis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to testis", "shortest_name_length": 20}
{"curie": "UMLS:C5206697", "names": ["Locally Advanced Urethral Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Urethral Urothelial Carcinoma", "shortest_name_length": 46}
{"curie": "UMLS:C3714208", "names": ["Blepharophimosis, Ptosis, and Epicanthus Inversus Type II", "BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS, TYPE II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Blepharophimosis, Ptosis, and Epicanthus Inversus Type II", "shortest_name_length": 57}
{"curie": "MONDO:0005041", "names": ["Glaucoma", "GLAUCOMA", "glaucoma", "glaucomas", "GLAUCOMAS", "Glaucomas", "Glaucoma NOS", "Glaucoma, NOS", "obsolete_glaucoma", "Glaucoma syndrome", "Glaucoma (H40-H42)", "glaucoma (disease)", "Glaucoma (disorder)", "Unspecified glaucoma", "glaucoma (diagnosis)", "Glaucoma, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glaucoma", "shortest_name_length": 8}
{"curie": "MONDO:0014718", "names": ["DEE34", "EIEE34", "early infantile epileptic encephalopathy 34", "epileptic encephalopathy, early infantile, 34", "developmental and epileptic encephalopathy 34", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 34", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 34", "developmental and epileptic encephalopathy, 34", "SLC12A5 early infantile epileptic encephalopathy", "epileptic encephalopathy, early infantile, type 34", "epileptic encephalopathy, early infantile, 34; EIEE34", "early infantile epileptic encephalopathy caused by mutation in SLC12A5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 34", "shortest_name_length": 5}
{"curie": "UMLS:C0040072", "names": ["Thymic Cyst", "thymic cyst", "thymus cyst", "Thymic cyst", "cyst; thymus", "cysts thymus", "thymus; cyst", "Thymic Cysts", "Cyst, Thymic", "THYMUS, CYST", "Cysts, Thymic", "Cyst of thymus", "Cyst of thymus gland", "Cyst of thymus gland (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thymic Cyst", "shortest_name_length": 11}
{"curie": "UMLS:C0392618", "names": ["Infection;post-op", "post-op infection", "infection post op", "infections post op", "Postoperative Infection", "Postoperative infection", "infection postoperative", "postoperative infection", "infections postoperative", "Postoperative infection NOS", "Postoperative infection (disorder)", "postoperative infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postoperative infection", "shortest_name_length": 17}
{"curie": "UMLS:C0392322", "names": ["Atypical schizophrenia", "atypical schizophrenia", "atypical; schizophrenic", "Atypical Schizophrenias", "Schizophrenia, atypical", "schizophrenia; atypical", "schizophrenia undifferentiated", "Undifferentiated Schizophrenia", "Undifferentiated schizophrenia", "undifferentiated schizophrenia", "undifferentiated; schizophrenic", "schizophrenia; undifferentiated", "Undifferentiated schizophrenia NOS", "Undifferentiated schizophrenia, NOS", "Undifferentiated Type Schizophrenia", "SCHIZOPHRENIA UNDIFFERENTIATED TYPE", "Schizophrenia, undifferentiated type", "Undifferentiated schizophrenia (disorder)", "undifferentiated schizophrenia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Undifferentiated schizophrenia", "shortest_name_length": 22}
{"curie": "MONDO:0018175", "names": ["F5F8D", "FV and FVIII combined deficiency", "Factor V and factor VIII combined deficiency", "combined deficiency of factor V and factor VIII", "familial multiple coagulation factor deficiency", "Combined Deficiency of Factor V and Factor VIII", "Combined deficiency of factor V and factor VIII", "Familial multiple coagulation factor deficiency", "FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF", "Factor V And Factor VIII, Combined Deficiency Of", "combined deficiency of factor V and factor type VIII", "Combined deficiency of factor V and factor VIII (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined deficiency of factor V and factor VIII", "shortest_name_length": 5}
{"curie": "UMLS:C0033119", "names": ["prick", "Prick", "pricks", "Puncture", "Punctured", "punctures", "PUNCTURES", "Puncture, NOS", "wound puncture", "puncture wound", "Puncture Wound", "PUNCTURE WOUND", "Puncture wound", "Wound, puncture", "puncture wounds", "Puncture wound - injury", "puncture wound (diagnosis)", "puncture wound (physical finding)", "Puncture (morphologic abnormality)", "Puncture wound - injury (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Puncture wound", "shortest_name_length": 5}
{"curie": "MONDO:0008919", "names": ["cud", "CUD", "SCD", "CDSP", "SPCD", "Carnitine deficiency", "Carnitine Deficiency", "carnitine uptake defect", "Carnitine uptake defect", "CARNITINE UPTAKE DEFECT", "Carnitine Uptake Deficiency", "Carnitine uptake deficiency", "Primary carnitine deficiency", "Primary Carnitine Deficiency", "Carnitine transporter defect", "primary carnitine deficiency", "systemic Carnitine deficiency", "SYSTEMIC CARNITINE DEFICIENCY", "Carnitine deficiency, primary", "CARNITINE DEFICIENCY, PRIMARY", "systemic carnitine deficiency", "Systemic carnitine deficiency", "Carnitine transporter deficiency", "carnitine transporter deficiency", "Renal Carnitine Transport Defect", "Carnitine Transporter Deficiency", "Renal carnitine transport defect", "renal carnitine transport defect", "Systemic primary carnitine deficiency", "systemic primary carnitine deficiency", "Systemic Primary Carnitine Deficiency", "Carnitine deficiency, systemic primary", "CARNITINE DEFICIENCY, SYSTEMIC PRIMARY", "CARNITINE deficiency, systemic primary", "primary carnitine deficiency (diagnosis)", "Renal carnitine transport defect (disorder)", "systemic primary carnitine deficiency disease", "Carnitine plasma-membrane transporter deficiency", "deficiency of plasma-membrane carnitine transporter", "Deficiency of plasma-membrane carnitine transporter", "Carnitine transporter, plasma-membrane, deficiency of", "CARNITINE TRANSPORTER, PLASMA-MEMBRANE, DEFICIENCY OF", "Carnitine transporter, plasma-Membrane, deficiency of", "Carnitine uptake deficiency/carnitine transport defect", "Carnitine deficiency, systemic, due to defect in renal reabsorption of carnitine", "CARNITINE DEFICIENCY, SYSTEMIC, DUE TO DEFECT IN RENAL REABSORPTION OF CARNITINE", "Carnitine deficiency, systemic, due to defect in renal reabsorption of Carnitine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "systemic primary carnitine deficiency disease", "shortest_name_length": 3}
{"curie": "UMLS:C4331225", "names": ["Recurrent Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma", "shortest_name_length": 65}
{"curie": "MONDO:0035540", "names": ["pheochromocytoma-paraganglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pheochromocytoma-paraganglioma", "shortest_name_length": 30}
{"curie": "MONDO:0012977", "names": ["DFNB1B", "autosomal recessive deafness 1B", "deafness, autosomal recessive 1b", "deafness, autosomal recessive 1B", "Deafness, Autosomal Recessive 1b", "DEAFNESS, AUTOSOMAL RECESSIVE 1B", "Autosomal recessive deafness type 1B", "deafness, autosomal recessive type 1B", "autosomal recessive nonsyndromic deafness 1B", "GJB6 autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 1B", "autosomal recessive nonsyndromic deafness type 1B", "autosomal recessive nonsyndromic deafness caused by mutation in GJB6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 1B", "shortest_name_length": 6}
{"curie": "MONDO:0012040", "names": ["IBD9", "inflammatory bowel disease 9", "Inflammatory Bowel Disease 9", "INFLAMMATORY BOWEL DISEASE 9", "inflammatory bowel disease type 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory bowel disease 9", "shortest_name_length": 4}
{"curie": "UMLS:C2698259", "names": ["MBL", "Monoclonal B-Cell Lymphocytosis", "monoclonal B-cell lymphocytosis", "Monoclonal B-cell lymphocytosis", "MBL - monoclonal B-cell lymphocytosis", "Monoclonal B-cell lymphocytosis (disorder)", "monoclonal B-cell lymphocytosis (diagnosis)", "Monoclonal B-cell lymphocytosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Monoclonal B-Cell Lymphocytosis", "shortest_name_length": 3}
{"curie": "MONDO:0013235", "names": ["Pnca2", "PNCA2", "pancreatic cancer 2", "BRCA2 familial pancreatic carcinoma", "susceptibility to pancreatic cancer 2", "PANCREATIC CANCER, SUSCEPTIBILITY TO, 2", "pancreatic cancer, susceptibility to, 2", "pancreatic cancer, susceptibility to, type 2", "familial pancreatic carcinoma caused by mutation in BRCA2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic cancer, susceptibility to, 2", "shortest_name_length": 5}
{"curie": "UMLS:C1290864", "names": ["abdomen disease", "abdomen diseases", "abdominal disorder", "disease of abdomen", "Abdominal disorder", "disorder of abdomen", "Disorder of abdomen", "abdominal disorders", "ABDOMINAL DISORDERS", "Disorder of abdomen (disorder)", "disorder of abdomen (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disorder of abdomen", "shortest_name_length": 15}
{"curie": "MONDO:0010653", "names": ["SHS", "RENS1", "MRX55", "Mrx55", "MRXS3", "MRXS8", "Porteous syndrome", "Porteous Syndrome", "Renpenning syndrome", "Renpenning Syndrome", "renpenning syndrome", "RENPENNING SYNDROME", "RENPENNING SYNDROME 1", "Renpenning syndrome 1", "Golabi-Ito-Hall syndrome", "GOLABI-ITO-HALL SYNDROME", "Sutherland-Haan syndrome", "Golabi-Ito-Hall Syndrome", "Renpenning syndrome type 1", "Renpenning syndrome (disorder)", "Sutherland-Haan syndrome (SHS)", "Mental Retardation, X-Linked 55", "MENTAL RETARDATION, X-LINKED 55", "mental retardation, X-linked 55", "renpenning syndrome (diagnosis)", "Hamel cerebropalatocardiac syndrome", "Hamel Cerebropalatocardiac Syndrome", "intellectual disability, X-linked 55", "X-linked mental retardation syndrome 3", "syndromic X-linked mental retardation 8", "renpenning syndrome, X-linked recessive", "X-linked mental retardation syndromic 3", "MENTAL RETARDATION, X-LINKED, SYNDROMIC 8", "MENTAL RETARDATION, X-LINKED, SYNDROMIC 3", "Mental retardation, X-linked, syndromic 8", "mental retardation, X-linked, syndromic 8", "Mental Retardation, X-Linked, Syndromic 3", "mental retardation, X-linked, syndromic 3", "X-linked mental retardation Renpenning type", "Mental retardation, X-linked Renpenning type", "syndromic X-linked intellectual disability 8", "X-linked intellectual disability syndromic 3", "mental retardation, X-linked Renpenning type", "mental retardation, X-linked, Renpenning type", "Mental Retardation, X-Linked, Renpenning Type", "MENTAL RETARDATION, X-LINKED, RENPENNING TYPE", "X-linked mental retardation syndrome 3 (MRXS3)", "X-Linked Intellectual Deficit, Renpenning Type", "intellectual disability, X-linked, syndromic 8", "intellectual disability, X-linked, syndromic 3", "X-linked intellectual disability Renpenning type", "intellectual disability, X-linked Renpenning type", "X-linked intellectual disability, Renpenning type", "X-linked mental retardation with spastic diplegia", "intellectual disability, X-linked, Renpenning type", "mental retardation, X-linked, with spastic diplegia", "Mental Retardation, X-Linked, With Spastic Diplegia", "MENTAL RETARDATION, X-LINKED, WITH SPASTIC DIPLEGIA", "X-linked intellectual deficit due to PQBP1 mutation", "Sutherland-Haan X-linked mental retardation syndrome", "X-Linked Intellectual Deficit Due To Pqbp1 Mutations", "SUTHERLAND-HAAN X-LINKED MENTAL RETARDATION SYNDROME", "X-linked mental retardation-spastic diplegia syndrome", "X-linked intellectual disability with spastic diplegia", "X-linked intellectual disability due to PQBP1 mutations", "intellectual disability, X-linked, with spastic diplegia", "Sutherland-Haan X-linked intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renpenning syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0002708", "names": ["RETINITIS", "retinitis", "Retinitis", "Retinitis NOS", "Retinitis, NOS", "Retina inflamed", "retina inflammation", "retina; inflammation", "Retinitis (disorder)", "inflammation; retina", "retinitis (diagnosis)", "swelling of the retina", "inflammation of retina", "Inflammation of retina"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis", "shortest_name_length": 9}
{"curie": "MONDO:0024318", "names": ["CNS Viral Disease", "Disease, CNS Viral", "Viral Disease, CNS", "CNS Viral Diseases", "Diseases, CNS Viral", "viral CNS infection", "Viral Diseases, CNS", "Viral CNS Infection", "CNS Infection, Viral", "Infection, Viral CNS", "Viral CNS Infections", "Infections, Viral CNS", "CNS Infections, Viral", "Infections, CNS, Viral", "Central Nervous System Viral Diseases", "Viral Diseases, Central Nervous System", "Central nervous system viral infection", "central nervous system viral infection", "Viral disease of central nervous system", "central nervous system; viral infection", "viral disease of central nervous system", "Central Nervous System Viral Infections", "virus; infection, central nervous system", "Viral Infections, Central Nervous System", "infection; central nervous system, viral", "infection; viral, central nervous system", "viral infection of central nervous system", "Viral infection of central nervous system", "Central nervous system viral infection NOS", "Viral infections of the central nervous system", "Viral infection of central nervous system (disorder)", "Unspecified viral infection of central nervous system", "viral infection of central nervous system (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "viral infection of central nervous system", "shortest_name_length": 17}
{"curie": "UMLS:C5237289", "names": ["Refractory Acute Graft Versus Host Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Acute Graft Versus Host Disease", "shortest_name_length": 42}
{"curie": "UMLS:C1142109", "names": ["Sopor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sopor", "shortest_name_length": 5}
{"curie": "MONDO:0018572", "names": ["severe intellectual disability-hypotonia-strabismus-coarse face-planovalgus syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe intellectual disability-hypotonia-strabismus-coarse face-planovalgus syndrome", "shortest_name_length": 84}
{"curie": "UMLS:C0349756", "names": ["AV Graft Stenosis", "Arteriovenous Graft Stenosis", "Arteriovenous graft stenosis", "Arteriovenous graft stenosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arteriovenous graft stenosis", "shortest_name_length": 17}
{"curie": "UMLS:C2981363", "names": ["Stage IIA Gastric Cancer", "stage IIA gastric cancer", "stage IIA gastric cancer AJCC v7", "Stage IIA Gastric Cancer AJCC v7", "Stage IIA Gastric (Stomach) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Gastric Cancer AJCC v7", "shortest_name_length": 24}
{"curie": "MONDO:0013217", "names": ["DBA10", "Diamond-Blackfan anemia 10", "DIAMOND-BLACKFAN ANEMIA 10", "Diamond-Blackfan Anemia 10", "RPS26 Diamond-Blackfan anemia", "Diamond-Blackfan Anemia type 10", "RPS26-related Diamond-Blackfan anemia", "Diamond-Blackfan anemia caused by mutation in RPS26"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diamond-Blackfan anemia 10", "shortest_name_length": 5}
{"curie": "MONDO:0001787", "names": ["INFARCT LIVER", "Liver Infarct", "Infarct liver", "Infarct, Liver", "Liver Infarcts", "Hepatic Infarct", "Hepatic infarct", "HEPATIC INFARCT", "Hepatic Infarcts", "Infarct of liver", "INFARCT OF LIVER", "liver infarction", "Infarct, Hepatic", "Liver Infarction", "infarction liver", "infarct of liver", "infarction; liver", "Infarction, Liver", "LIVER, INFARCTION", "Liver Infarctions", "liver; infarction", "Hepatic Infarction", "HEPATIC INFARCTION", "hepatic infarction", "Hepatic infarction", "Infarction of liver", "Infarction, Hepatic", "Hepatic Infarctions", "Hepatic infarction (disorder)", "hepatic infarction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatic infarction", "shortest_name_length": 13}
{"curie": "MONDO:0013662", "names": ["BE", "CLE", "CELLO", "cello", "Barrett", "barrett ulcer", "Barrett; ulcer", "ulcer; Barrett", "ULCER, BARRETT", "Barrett's ulcer", "Barret syndrome", "barrett's ulcers", "Ulcer, Barrett's", "barrett syndrome", "Barrett Syndrome", "ESOPHAGUS BARRETT", "barretts syndrome", "BARRETT ESOPHAGUS", "Barretts syndrome", "barrett esophagus", "Barrett esophagus", "Barrett's disease", "Barretts Syndrome", "Barrett Esophagus", "Barrett metaplasia", "BARRETT METAPLASIA", "barrett's syndrome", "Barrett's Syndrome", "Barrett Metaplasia", "ESOPHAGUS, BARRETT", "Esophagus, Barrett", "Barretts esophagus", "Barrett oesophagus", "Barrett's syndrome", "Barretts Esophagus", "barrett esophagitis", "BARRETT'S ESOPHAGUS", "Barrett's Esophagus", "Barrett Metaplasias", "Barrett's esophagus", "Metaplasia, Barrett", "barrett's esophagus", "Endobrachyesophagus", "Barretts esophagitis", "Esophagus, Barrett's", "Endobrachyoesophagus", "Barrett's oesophagus", "Metaplasias, Barrett", "barrett's oesophagus", "barrett oesophagitis", "Barretts oesophagitis", "Barrett's Esophagitis", "Endobrachyooesophagus", "barrett's esophagitis", "Oesophagitis;Barretts", "Barrett's esophagitis", "barrett's oesophagitis", "Barrett's oesophagitis", "ulcerative esophagitis", "Barrett's esophagus NOS", "Columnar-Lined Esophagus", "Columnar-lined esophagus", "columnar-lined esophagus", "BO - Barrett's esophagus", "Columnar-lined oesophagus", "BO - Barrett's oesophagus", "ESOPHAGUS, COLUMNAR-LINED", "Barrett ulcer of esophagus", "adenocarcinoma of esophagus", "Barrett ulcer of oesophagus", "Barrett's ulcer of esophagus", "Barrett's ulcer of oesophagus", "CLE - Columnar-lined esophagus", "Barrett's esophagus (disorder)", "CLE - Columnar-lined oesophagus", "Barrett's esophagus (diagnosis)", "Gastric metaplasia of esophagus", "Gastric metaplasia of oesophagus", "Barrett's esophagus with esophagitis", "Barrett's ulcer of esophagus (disorder)", "Columnar epithelial-lined lower esophagus", "columnar epithelial-lined Lower esophagus", "Columnar Epithelial-Lined Lower Esophagus", "Columnar epithelial-lined lower oesophagus", "Barrett esophagus/esophageal adenocarcinoma", "CELLO - Columnar epithelial-lined lower esophagus", "CELLO - Columnar epithelial-lined lower oesophagus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Barrett esophagus", "shortest_name_length": 2}
{"curie": "UMLS:C4745367", "names": ["Thyroid Gland Malignant Peripheral Nerve Sheath Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Malignant Peripheral Nerve Sheath Tumor", "shortest_name_length": 53}
{"curie": "MONDO:0020947", "names": ["PARASITIC EYE INFECT", "EYE INFECT PARASITIC", "Parasitic Eye Infection", "OCULAR INFECT PARASITIC", "Parasitic eye infection", "parasitic eye infection", "Infection, Parasitic Eye", "Parasitic Eye Infections", "Eye Infection, Parasitic", "Infections, Parasitic Eye", "Eye Infections, Parasitic", "Parasitic Ocular Infection", "Infection, Parasitic Ocular", "Parasitic Ocular Infections", "Ocular Infection, Parasitic", "Ocular Infections, Parasitic", "Infections, Parasitic Ocular", "Parasitic eye infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parasitic eye infection", "shortest_name_length": 20}
{"curie": "UMLS:C0235863", "names": ["delayed delivery", "Delivery delayed", "DELIVERY DELAYED", "delivery delayed", "Delayed delivery", "delivery; delayed", "delayed; delivery"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Delayed delivery", "shortest_name_length": 16}
{"curie": "MONDO:0002085", "names": ["Shuddering attacks", "benign shuddering attacks", "Benign shuddering attacks", "Shuddering attacks (disorder)", "benign shuddering attacks (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign shuddering attacks", "shortest_name_length": 18}
{"curie": "MONDO:0017946", "names": ["HCHWA, Iowa type", "ABetaD23N amyloidosis", "ABeta amyloidosis, Iowa type", "cerebral amyloid angiopathy, APP-related, Iowa variant", "hereditary cerebral hemorrhage with amyloidosis, Iowa type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ABeta amyloidosis, Iowa type", "shortest_name_length": 16}
{"curie": "MONDO:0010250", "names": ["MRX49", "MRX15", "MRXSRC", "Raynaud Claes syndrome", "Raynaud-Claes syndrome", "RAYNAUD-CLAES SYNDROME", "X-linked mental retardation 15", "X-linked mental retardation 49", "mental retardation, X-linked 15", "MENTAL RETARDATION, X-LINKED 49", "mental retardation, X-linked 49", "MENTAL RETARDATION, X-LINKED 15", "intellectual disability, X-linked 15", "intellectual disability, X-linked 49", "raynaud-claes syndrome, X-linked dominant", "X-linked mental retardation 15 (MRX15, XLMR15)", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 49", "CLCN4-related X-linked intellectual disability syndrome", "Chloride voltage-gated channel 4-related X-linked intellectual disability syndrome", "Chloride voltage-gated channel 4-related X-linked intellectual disability syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 49", "shortest_name_length": 5}
{"curie": "MONDO:0017811", "names": ["Del(5)(q31.3)", "monosomy 5q31.3", "Monosomy 5q31.3", "5q31.3 microdeletion syndrome", "5q31.3 microdeletion syndrome (disorder)", "5q31.3 microdeletion syndrome (diagnosis)", "severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion", "Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion", "Severe neonatal hypotonia, seizures, encephalopathy syndrome due to 5q31.3 microdeletion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion", "shortest_name_length": 13}
{"curie": "MONDO:0017547", "names": ["congenital vertical talus, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital vertical talus, bilateral", "shortest_name_length": 36}
{"curie": "MONDO:0003679", "names": ["asmi", "MYOCARDIAL INFARCTION ANTEROSEPTAL", "anteroseptal myocardial infarction", "Anteroseptal Myocardial Infarction", "Infarction, Anteroseptal Myocardial", "Myocardial Infarction, Anteroseptal", "Anteroseptal Myocardial Infarctions", "Infarctions, Anteroseptal Myocardial", "MYOCARDIAL INFARCTION (ANTEROSEPTAL)", "Myocardial Infarctions, Anteroseptal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anteroseptal myocardial infarction", "shortest_name_length": 4}
{"curie": "MONDO:0001568", "names": ["Mixed receptive language disorder", "mixed receptive-expressive language disorder", "Mixed Receptive-Expressive Language Disorder", "Mixed receptive-expressive language disorder", "language disorder; mixed receptive and expressive", "disorder; mixed, language, receptive and expressive", "mixed; disorder, language, receptive and expressive", "mixed; language disorder (receptive and expressive)", "Mixed receptive-expressive language disorder (disorder)", "mixed receptive-expressive language disorder (diagnosis)", "mixed receptive-expressive language developmental disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed receptive-expressive language disorder", "shortest_name_length": 33}
{"curie": "MONDO:0008732", "names": ["adrenal hypoplasia, cytomegalic type", "ADRENAL HYPOPLASIA, CYTOMEGALIC TYPE", "Adrenal Hypoplasia, Cytomegalic Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adrenal hypoplasia, cytomegalic type", "shortest_name_length": 36}
{"curie": "MONDO:0013281", "names": ["CDG2J", "CDGIIj", "CDGIIdj", "CDG IIj", "CDG-IIj", "COG4-CDG", "COG4-CDG (CDG-IIj)", "CDG syndrome type IIj", "COG4 congenital disorder of glycosylation", "COG4-congenital disorder of glycosylation", "Congenital disorder of glycosylation type 2j", "congenital disorder of glycosylation type 2j", "Congenital disorder of glycosylation type IIj", "congenital disorder of glycosylation type IIj", "congenital disorder of glycosylation, type IIj", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj", "Carbohydrate deficient glycoprotein syndrome type 2j", "carbohydrate deficient glycoprotein syndrome type IIj", "Carbohydrate deficient glycoprotein syndrome type IIj", "CDG2J - carbohydrate deficient glycoprotein syndrome type 2J", "Component of oligomeric golgi complex 4 congenital disorder of glycosylation", "COG4 (component of oligomeric golgi complex 4) congenital disorder of glycosylation", "Component of oligomeric golgi complex 4 congenital disorder of glycosylation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "COG4-congenital disorder of glycosylation", "shortest_name_length": 5}
{"curie": "UMLS:C1511315", "names": ["Breast Inflammatory Myofibroblastic Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Inflammatory Myofibroblastic Tumor", "shortest_name_length": 41}
{"curie": "MONDO:0010570", "names": ["CFNS", "CFND", "CRANIOFRONTONASAL SYNDROME", "Craniofrontonasal syndrome", "craniofrontonasal syndrome", "Craniofrontonasal dysplasia", "CRANIOFRONTONASAL DYSPLASIA", "craniofrontonasal dysplasia", "Craniofrontonasal dysostosis", "craniofrontonasal dysostosis", "CRANIOFRONTONASAL DYSOSTOSIS", "craniofrontonasal syndrome (CNFS)", "craniofrontonasal dysplasia (CFND)", "Craniofrontonasal dysplasia (disorder)", "craniofrontonasal dysplasia, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniofrontonasal syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0743568", "names": ["Unresectable Esophageal Cancer", "Esophageal Cancer Unresectable", "ESOPHAGEAL CANCER UNRESECTABLE", "Unresectable Cancer of Esophagus", "Esophageal Carcinoma Unresectable", "Unresectable Esophageal Carcinoma", "Unresectable Cancer of the Esophagus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Esophageal Carcinoma", "shortest_name_length": 30}
{"curie": "UMLS:C1333598", "names": ["FAP Associated Medulloblastoma", "Familial Adenomatous Polyposis Associated Medulloblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Familial Adenomatous Polyposis Associated Medulloblastoma", "shortest_name_length": 30}
{"curie": "UMLS:C4054379", "names": ["Nephrotic Syndrome - LAMB2 Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - LAMB2 Associated", "shortest_name_length": 37}
{"curie": "MONDO:0043297", "names": ["vibrio vulnificus infection", "Vibrio vulnificus infection", "vibrio vulnificus infectious disease", "Vibrio vulnificus infectious disease", "Vibrio vulnificus disease or disorder", "Vibrio vulnificus infection (disorder)", "Vibrio vulnificus caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vibrio vulnificus infectious disease", "shortest_name_length": 27}
{"curie": "MONDO:0022737", "names": ["choroideremia hypopituitarism", "choroideraemia hypopituitarism", "choroideremia with hypopituitarism", "choroideremia with hypopituitarism (diagnosis)", "choroideremia co-occurrent with hypopituitarism", "choroideraemia co-occurrent with hypopituitarism", "hereditary choroidal dystrophy choroideremia with hypopituitarism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choroideremia hypopituitarism", "shortest_name_length": 29}
{"curie": "UMLS:C3165209", "names": ["HDL-deficiency", "High-density lipoprotein deficiency", "High density lipoprotein deficiency", "deficiency; high-density lipoprotein", "high-density lipoprotein; deficiency", "High density lipoprotein deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High density lipoprotein deficiency", "shortest_name_length": 14}
{"curie": "MONDO:0009998", "names": ["RCPS", "Richieri-Costa-Pereira Syndrome", "Richieri Costa Pereira syndrome", "Richieri-Costa-Pereira syndrome", "Richieri Costa-Pereira syndrome", "RICHIERI-COSTA-PEREIRA SYNDROME", "ROBIN sequence with cleft mandible and limb anomalies", "Robin sequence with cleft mandible and limb anomalies", "ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES", "Richieri-Costa and Pereira form of acrofacial dysostosis", "Robin sequence with cleft mandible and limb anomalies syndrome", "short stature-Pierre Robin sequence-cleft mandible-hand anomalies clubfoot syndrome", "Short stature-Pierre Robin sequence-cleft mandible-hand anomalies clubfoot syndrome", "short stature-Pierre Robin syndrome-cleft mandible-hand anomalies clubfoot syndrome", "Short stature-Pierre Robin syndrome-cleft mandible-hand anomalies clubfoot syndrome", "Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome", "short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfoot", "Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Richieri Costa-Pereira syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0009750", "names": ["HMSN with excessive myelin Outfolding, autosomal recessive", "HMSN WITH EXCESSIVE MYELIN OUTFOLDING, AUTOSOMAL RECESSIVE", "CHARCOT-MARIE-TOOTH DISEASE WITH EXCESSIVE MYELIN FOLDING, AUTOSOMAL RECESSIVE", "Charcot-Marie-Tooth Disease with Excessive Myelin Folding, Autosomal Recessive", "Charcot-Marie-Tooth disease with excessive myelin folding, autosomal recessive", "Neuropathy, Hereditary Motor and Sensory, with Excessive Myelin Folding Complex, Autosomal Recessive", "NEUROPATHY, HEREDITARY MOTOR AND SENSORY, WITH EXCESSIVE MYELIN FOLDING COMPLEX, AUTOSOMAL RECESSIVE", "neuropathy, hereditary motor and sensory, with excessive myelin folding complex, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuropathy, hereditary motor and sensory, with excessive myelin folding complex, autosomal recessive", "shortest_name_length": 58}
{"curie": "MONDO:0022945", "names": ["deafness peripheral neuropathy arterial disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness peripheral neuropathy arterial disease", "shortest_name_length": 47}
{"curie": "UMLS:C4520749", "names": ["Stage II Laryngeal Cancer", "stage II laryngeal cancer", "Stage II Larynx Carcinoma", "Laryngeal Cancer, Stage II", "Stage II Laryngeal Carcinoma", "Stage II Carcinoma of Larynx", "Stage II Laryngeal Throat Cancer", "Stage II Carcinoma of the Larynx", "Stage II Laryngeal Cancer AJCC v7", "Stage II Laryngeal Cancer AJCC v6", "Stage II Laryngeal Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Laryngeal Cancer AJCC v6 and v7", "shortest_name_length": 25}
{"curie": "MONDO:0014724", "names": ["JBTS24", "JOUBERT SYNDROME 24", "Joubert syndrome 24", "TCTN2 Joubert syndrome", "Joubert syndrome type 24", "Joubert syndrome caused by mutation in TCTN2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome 24", "shortest_name_length": 6}
{"curie": "UMLS:C4727151", "names": ["Recurrent Hemophagocytic Lymphohistiocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Hemophagocytic Lymphohistiocytosis", "shortest_name_length": 44}
{"curie": "MONDO:0007374", "names": ["SCD", "SCCD", "SCHNYDER CORNEAL DYSTROPHY", "Schnyder corneal dystrophy", "CORNEAL DYSTROPHY, SCHNYDER", "corneal dystrophy, Schnyder", "Crystalline corneal dystrophy", "Crystalline stromal dystrophy", "corneal dystrophy crystalline", "crystalline stromal dystrophy", "corneal dystrophy, Schnyder type", "Schnyder crystalline cornea dystrophy", "SCHNYDER CRYSTALLINE CORNEAL DYSTROPHY", "corneal dystrophy Schnyder crystalline", "Schnyder crystalline corneal dystrophy", "Crystalline corneal dystrophy (disorder)", "Schnyder's crystalline corneal dystrophy", "corneal dystrophy crystalline of Schnyder", "Corneal dystrophy crystalline of Schnyder", "Crystalline corneal dystrophy (diagnosis)", "corneal dystrophy, crystalline, of Schnyder", "Corneal Dystrophy, Crystalline, of Schnyder", "CORNEAL DYSTROPHY, CRYSTALLINE, OF SCHNYDER", "Schnyder crystalline dystrophy sine crystals", "Schnyder crystalline cornea dystrophy (disorder)", "Schnyder crystalline corneal dystrophy (diagnosis)", "Hereditary crystalline stromal dystrophy of Schnyder", "hereditary crystalline stromal dystrophy of Schnyder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Schnyder corneal dystrophy", "shortest_name_length": 3}
{"curie": "MONDO:0000666", "names": ["associative agnosia", "associative visual agnosia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "associative visual agnosia", "shortest_name_length": 19}
{"curie": "MONDO:0017533", "names": ["postaxial polydactyly type B, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postaxial polydactyly type B, unilateral", "shortest_name_length": 40}
{"curie": "MONDO:0043267", "names": ["vasculitis rheumatoid", "rheumatoid vasculitis", "Rheumatoid vasculitis", "RHEUMATOID VASCULITIS", "Rheumatoid Vasculitis", "vasculitis, rheumatoid", "Vasculitis, Rheumatoid", "rheumatoid; vasculitis", "vasculitis; rheumatoid", "Rheumatoid Vasculitides", "rheumatoid Vasculitides", "Vasculitides, rheumatoid", "Vasculitides, Rheumatoid", "rheumatoid vasculitis (diagnosis)", "Rheumatoid arthritis with vasculitis", "arthritis; rheumatoid, with vasculitis", "rheumatoid; arthritis, with vasculitis", "Rheumatoid arthritis with vasculitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rheumatoid vasculitis", "shortest_name_length": 21}
{"curie": "UMLS:C3888466", "names": ["Medical device site discharge"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Medical device site discharge", "shortest_name_length": 29}
{"curie": "MONDO:0011998", "names": ["SNCV", "slowed nerve conduction velocity, AD", "Autosomal dominant slowed nerve conduction velocity", "autosomal dominant slowed nerve conduction velocity", "Slowed Nerve Conduction Velocity, Autosomal Dominant", "SLOWED NERVE CONDUCTION VELOCITY, AUTOSOMAL DOMINANT", "slowed nerve conduction velocity, autosomal dominant", "Autosomal dominant slowed nerve conduction velocity (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant slowed nerve conduction velocity", "shortest_name_length": 4}
{"curie": "MONDO:0008742", "names": ["SCN1", "Autosomal Dominant SCN", "autosomal dominant severe congenital neutropenia", "Autosomal dominant severe congenital neutropenia", "severe congenital neutropenia autosomal dominant", "Autosomal Dominant Severe Congenital Neutropenia", "Autosomal dominant severe congenital neutropaenia", "severe congenital neutropenia, autosomal dominant", "Neutropenia, Severe Congenital, Autosomal Dominant 1", "Neutropenia, Severe Congenital, 1, Autosomal Dominant", "NEUTROPENIA, SEVERE CONGENITAL, 1, AUTOSOMAL DOMINANT", "Severe Congenital Neutropenia Type 1, Autosomal Dominant", "Autosomal dominant severe congenital neutropenia (disorder)", "Severe Congenital neutropenia (SCN) 1 -  Includes cyclic neutropenia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant severe congenital neutropenia", "shortest_name_length": 4}
{"curie": "MONDO:0002768", "names": ["herm", "herms", "Herms", "Intersex", "OVOTESTIS", "ovotestis", "Ovotestis", "Hermaphrodite", "hermaphrodism", "HERMAPHRODITE", "Hermaphrodism", "intersexuality", "Intersexuality", "HERMAPHRODITISM", "hermaphroditism", "Hermaphroditism", "true hermaphrodite", "True hermaphrodite", "hermaphrodites true", "true hermaphroditism", "True Hermaphroditism", "True hermaphroditism", "True Hermaphroditisms", "Hermaphroditism, True", "HERMAPHRODITISM, TRUE", "Hermaphroditisms, True", "Hermaphroditism syndrome", "hermaphroditism (diagnosis)", "Familial True Hermaphroditism", "Hermaphroditism syndrome, true", "Familial True Hermaphroditisms", "Hermaphroditism, Familial True", "True Hermaphroditism, Familial", "True Hermaphroditisms, Familial", "Hermaphroditisms, Familial True", "True Hermaphroditism (disorder)", "Testicular and ovarian tissue present"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "true hermaphroditism", "shortest_name_length": 4}
{"curie": "MONDO:0012390", "names": ["ARTHROGRYPOSIS MULTIPLEX WITH DEAFNESS, INGUINAL HERNIAS, AND EARLY DEATH", "Arthrogryposis multiplex with deafness, inguinal hernias, and early death", "arthrogryposis multiplex with deafness, inguinal hernias, and early death"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis multiplex with deafness, inguinal hernias, and early death", "shortest_name_length": 73}
{"curie": "MONDO:0002117", "names": ["pancreas sarcoma", "Pancreatic sarcoma", "Pancreatic Sarcoma", "pancreatic sarcoma", "sarcoma of pancreas", "Sarcoma of Pancreas", "Sarcoma of the Pancreas", "sarcoma of the pancreas", "sarcoma of pancreas (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreas sarcoma", "shortest_name_length": 16}
{"curie": "UMLS:C1333049", "names": ["Cigarette Smoking-Related Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cigarette Smoking-Related Carcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C4520764", "names": ["Melanoma in situ", "Stage 0 Melanoma", "Melanoma In Situ", "melanoma in situ", "stage 0 melanoma", "Skin Melanoma in situ", "Melanoma in situ of Skin", "Stage 0 Melanoma of Skin", "Cutaneous Melanoma in situ", "Stage 0 Cutaneous Melanoma", "Stage 0 Malignant Melanoma", "Stage 0 Melanoma of the Skin", "Melanoma in situ of the Skin", "Stage 0 Skin Melanoma AJCC v6", "Stage 0 Skin Melanoma AJCC v7", "Malignant Skin Melanoma in situ", "Stage 0 Malignant Skin Melanoma", "Stage 0 Cutaneous (Skin) Melanoma", "Stage 0 Skin Melanoma AJCC v6 and v7", "Stage 0 Malignant Cutaneous Melanoma", "Malignant Cutaneous Melanoma in situ", "Stage 0 Cutaneous Melanoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Cutaneous Melanoma AJCC v6 and v7", "shortest_name_length": 16}
{"curie": "UMLS:C0279556", "names": ["ductal invasive breast carcinoma with predominant intraductal component", "Invasive Ductal Breast Carcinoma with Predominant Intraductal Component", "invasive ductal breast carcinoma with predominant intraductal component", "Invasive Breast Ductal Carcinoma with Predominant Intraductal Component", "Infiltrating Ductal Breast Carcinoma with Predominant Intraductal Component", "Invasive Breast Carcinoma of No Special Type with Predominant Intraductal Component"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Invasive Breast Carcinoma of No Special Type with Predominant Intraductal Component", "shortest_name_length": 71}
{"curie": "MONDO:0023820", "names": ["Moebius axonal neuropathy hypogonadism", "Moebius syndrome with hypogonadotrophic hypogonadism and progressive peripheral neuropathy axonal and demyelinating type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Moebius axonal neuropathy hypogonadism", "shortest_name_length": 38}
{"curie": "UMLS:C0280790", "names": ["Anaplastic Oligodendroglioma", "adult anaplastic oligodendroglioma", "Adult Anaplastic Oligodendroglioma", "anaplastic oligodendroglioma, adult", "oligodendroglioma, adult anaplastic", "Adult Undifferentiated Oligodendroglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Anaplastic Oligodendroglioma", "shortest_name_length": 28}
{"curie": "MONDO:0042962", "names": ["Slti-Salem syndrome", "Slti Salem syndrome", "hypogonadotropic hypogonadism alopecia", "Hypogonadotropic hypogonadism alopecia", "hypogonadism and frontoparietal alopecia", "Hypogonadism and frontoparietal alopecia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Slti-Salem syndrome", "shortest_name_length": 19}
{"curie": "MONDO:0013854", "names": ["CILD17", "primary ciliary dyskinesia 17", "ciliary dyskinesia, primary, 17", "CILIARY DYSKINESIA, PRIMARY, 17", "primary ciliary dyskinesia type 17", "CCDC103 primary ciliary dyskinesia", "ciliary dyskinesia, primary, type 17", "primary ciliary dyskinesia caused by mutation in CCDC103", "primary ciliary dyskinesia 17 with or without situs inversus", "CILIARY DYSKINESIA, PRIMARY, 17, WITH OR WITHOUT SITUS INVERSUS", "ciliary dyskinesia, primary, 17, with or without situs inversus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia 17", "shortest_name_length": 6}
{"curie": "DOID:0080577", "names": ["polygenic disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polygenic disease", "shortest_name_length": 17}
{"curie": "UMLS:C2721720", "names": ["Reduced bladder capacity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reduced bladder capacity", "shortest_name_length": 24}
{"curie": "MONDO:0012908", "names": ["C6D", "C6 Deficiency", "C6 deficiency", "C6 DEFICIENCY", "C6 DEFICIENCY, SUBTOTAL", "C6 Deficiency, Subtotal", "C6 deficiency, subtotal", "complement component 6 deficiency", "Complement Component 6 Deficiency", "COMPLEMENT COMPONENT 6 DEFICIENCY", "Complement Component 6 Deficiency, Subtotal", "COMPLEMENT COMPONENT 6 DEFICIENCY, SUBTOTAL", "complement component 6 deficiency, subtotal", "C6 classic complement early component deficiency", "classic complement early component deficiency caused by mutation in C6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complement component 6 deficiency", "shortest_name_length": 3}
{"curie": "MONDO:0006219", "names": ["Gallbladder Small Cell NEC", "gallbladder small cell NEC", "gallbladder Oat cell carcinoma", "Gallbladder Oat Cell Carcinoma", "gallbladder small cell carcinoma", "Gallbladder Small Cell Carcinoma", "gall bladder small cell carcinoma", "Oat Cell Carcinoma of Gallbladder", "Oat cell carcinoma of gallbladder", "small cell carcinoma of gallbladder", "Small Cell Carcinoma of Gallbladder", "small cell carcinoma of gall bladder", "Oat cell carcinoma of the gallbladder", "Oat Cell Carcinoma of the Gallbladder", "Small Cell Carcinoma of the Gallbladder", "small cell carcinoma of the gallbladder", "small cell carcinoma of gallbladder (diagnosis)", "gallbladder small cell neuroendocrine carcinoma", "Gallbladder Small Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gallbladder small cell neuroendocrine carcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0000387", "names": ["microcytic/hypochromic anemia", "Microcytic hypochromic anemia", "ANEMIA MICROCYTIC HYPOCHROMIC", "hypochromic microcytic anemia", "microcytic hypochromic anemia", "Hypochromic microcytic anemia", "anemia microcytic hypochromic", "microcytic hypochromic anaemia", "Microcytic, hypochromic anemia", "Hypochromic microcytic anaemia", "Anemia, hypochromic microcytic", "anemias hypochromic microcytic", "hypochromic microcytic anaemia", "Anemia, microcytic hypochromic", "Hypochromic, microcytic anemia", "Microcytic hypochromic anaemia", "anemia; hypochromic, microcytic", "hypochromic / microcytic anemia", "anemia; microcytic, hypochromic", "Hypochromic, microcytic anaemia", "Anemia- Hypochromic microcytic picture", "Anaemia- Hypochromic microcytic picture", "hypochromic microcytic anemia (disease)", "Microcytic hypochromic anemia (disorder)", "hypochromic microcytic anemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypochromic microcytic anemia", "shortest_name_length": 29}
{"curie": "UMLS:C4330007", "names": ["Fourth Ventricle and Brain Stem Ependymal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fourth Ventricle and Brain Stem Ependymal Tumor", "shortest_name_length": 47}
{"curie": "MONDO:0007293", "names": ["lad", "LAD", "Lad1", "LAD1", "lad-I", "lad 1", "LAD-1", "LAD-I", "lad-type I", "LAD-Type I", "Mo-1 deficiency", "LAD-1 Deficiency", "LFA-I Deficiency", "LFA-I deficiency", "LFA-1 deficiency", "LFA1 IMMUNODEFICIENCY", "Lfa1 immunodeficiency", "LFA1 Immunodeficiency", "Lfa1 Immunodeficiency", "LFA1 immunodeficiency", "LFA 1 immunodeficiency", "leukocyte adhesion deficiency", "LEUKOCYTE ADHESION DEFICIENCY", "leukocyte adhesion deficiency 1", "leukocyte adhesion defect - type I", "ITGB2 leukocyte adhesion deficiency", "leukocyte adhesion deficiency type 1", "Leukocyte adhesion deficiency type I", "leukocyte adhesion deficiency type I", "Leukocyte Adhesion Deficiency Type 1", "Leukocyte adhesion deficiency type 1", "leukocyte adhesion deficiency, type I", "leukocyte adhesion deficiency, type 1", "LEUKOCYTE ADHESION DEFICIENCY, TYPE I", "Leukocyte Adhesion Deficiency, Type I", "Leucocyte adhesion deficiency - type 1", "Leukocyte adhesion deficiency - type 1", "LAD - Leukocyte adhesion deficiency type 1", "LAD - Leucocyte adhesion deficiency type 1", "leukocyte adhesion defect - type I (diagnosis)", "Leukocyte adhesion molecule deficiency - type 1", "Leucocyte adhesion molecule deficiency - type 1", "Leukocyte adhesion deficiency - type 1 (disorder)", "leukocyte adhesion deficiency caused by mutation in ITGB2", "Lymphocyte function-associated antigen 1 immunodeficiency", "LYMPHOCYTE FUNCTION-ASSOCIATED ANTIGEN 1 IMMUNODEFICIENCY", "lymphocyte function-associated antigen 1 immunodeficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukocyte adhesion deficiency 1", "shortest_name_length": 3}
{"curie": "MONDO:0030837", "names": ["NEDMILEG", "NEDMILEG, AD", "neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities", "NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, IMPAIRED LANGUAGE, EPILEPSY, AND GAIT ABNORMALITIES", "neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities", "shortest_name_length": 8}
{"curie": "MONDO:0018956", "names": ["bronchiectasis idiopathic", "Idiopathic bronchiectasis", "idiopathic bronchiectasis", "Idiopathic bronchiectasis (disorder)", "Idiopathic bronchiectasis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic bronchiectasis", "shortest_name_length": 25}
{"curie": "UMLS:C4683559", "names": ["Mycosis Fungoides and Sezary Syndrome by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mycosis Fungoides and Sezary Syndrome by AJCC v7 Stage", "shortest_name_length": 54}
{"curie": "UMLS:C5235852", "names": ["Advanced Urethral Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Urethral Urothelial Carcinoma", "shortest_name_length": 38}
{"curie": "MONDO:0045052", "names": ["Benign Osseous Tumor", "benign osseous tumor", "Benign Osseous Neoplasm", "benign osseous neoplasm", "Benign osteogenic tumor", "Benign Osteogenic Tumor", "benign osteogenic tumor", "Benign osteogenic tumour", "benign osteogenic neoplasm", "Benign Osteogenic Neoplasm", "Benign osteogenic neoplasm", "osteogenic neoplasm, benign", "Benign osteogenic neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign osteogenic neoplasm", "shortest_name_length": 20}
{"curie": "MONDO:0008733", "names": ["GCCD", "glucocorticoid deficiency", "Familial glucocorticoid deficiency", "Isolated Glucocorticoid Deficiency", "Familial Glucocorticoid Deficiency", "familial glucocorticoid deficiency", "Familial Glucocorticoid Deficiency 1", "Familial glucocorticoid deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial glucocorticoid deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0011007", "names": ["froster syndrome", "FROSTER SYNDROME", "froster-Huch syndrome", "Froster Huch syndrome", "Froster-Huch syndrome", "diaphragmatic defect limb deficiency skull defect", "Diaphragmatic defect-limb deficiency-skull defect syndrome", "diaphragmatic defect-limb deficiency-skull defect syndrome", "Diaphragmatic defect, limb deficiency, skull defect syndrome", "Diaphragmatic defect, limb deficiency, skull defect syndrome (disorder)", "DIAPHRAGMATIC DEFECTS, LIMB DEFICIENCIES, AND OSSIFICATION DEFECTS OF SKULL", "Diaphragmatic Defects, Limb Deficiencies, and Ossification Defects Of Skull", "diaphragmatic defects, limb deficiencies, and ossification defects of skull"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diaphragmatic defect-limb deficiency-skull defect syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0022800", "names": ["COL2A1", "collagen II", "Cartilage collagen", "cartilage collagen", "type 2 collagenopathy", "COL2A1 disease or disorder", "collagenopathy type 2 alpha 1", "Collagenopathy, type 2 alpha 1", "disease or disorder caused by mutation in COL2A1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type 2 collagenopathy", "shortest_name_length": 6}
{"curie": "MONDO:0020496", "names": ["familial porencephaly", "hereditary porencephaly", "brain small vessel disease", "familial porencephalic white matter disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial porencephaly", "shortest_name_length": 21}
{"curie": "MONDO:0007794", "names": ["IHH", "HH7", "Idiopathic gonadotrophin deficiency", "hypogonadism, isolated hypogonadotropic", "IDIOPATHIC HYPOGONADOTROPIC HYPOGONADISM", "Idiopathic hypogonadotropic hypogonadism", "idiopathic hypogonadotropic hypogonadism", "Idiopathic Hypogonadotropic Hypogonadism", "hypogonadotropic hypogonadism 7 without anosmia", "Idiopathic hypogonadotropic hypogonadism (disorder)", "Hypogonadotropic Hypogonadism 7 With Or Without Anosmia", "hypogonadotropic hypogonadism 7 with or without anosmia", "HYPOGONADOTROPIC HYPOGONADISM 7 WITH OR WITHOUT ANOSMIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadotropic hypogonadism 7 with or without anosmia", "shortest_name_length": 3}
{"curie": "UMLS:C5206450", "names": ["Stage IIIB Cervical Cancer FIGO 2018", "Stage IIIB Cervical Carcinoma FIGO 2018"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Cervical Cancer FIGO 2018", "shortest_name_length": 36}
{"curie": "UMLS:C0855036", "names": ["Alveolar Soft Part Sarcoma Metastatic", "Alveolar soft part sarcoma metastatic", "Metastatic Alveolar Soft Part Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alveolar soft part sarcoma metastatic", "shortest_name_length": 37}
{"curie": "MONDO:0003745", "names": ["Choroid Spindle Cell Melanoma", "choroid spindle cell melanoma", "spindle cell melanoma of choroid", "Spindle Cell Melanoma of Choroid", "optic choroid spindle cell melanoma", "Spindle Cell Melanoma of the Choroid", "spindle cell melanoma of the Choroid", "spindle cell melanoma of the choroid", "spindle cell melanoma of optic choroid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choroid spindle cell melanoma", "shortest_name_length": 29}
{"curie": "UMLS:C0278875", "names": ["Craniopharyngioma", "Adult Craniopharyngioma", "adult craniopharyngioma", "Craniopharyngioma, Adult", "craniopharyngioma, adult", "Adult Craniopharyngiomas", "Adult Rathke Pouch Tumor", "Craniopharyngiomas, Adult", "Adult Rathke's Pouch Tumor", "Adult Tumor of Rathke's Pouch", "Adult Rathke's Pouch Neoplasm", "Adult Neoplasm of Rathke's Pouch", "adult CNS tumor, craniopharyngioma", "CNS tumor, adult craniopharyngioma", "CNS tumor, craniopharyngioma, adult", "brain tumor, adult craniopharyngioma", "adult brain tumor, craniopharyngioma", "brain tumor, craniopharyngioma, adult", "central nervous system tumor, craniopharyngioma, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Craniopharyngioma", "shortest_name_length": 17}
{"curie": "UMLS:C1561828", "names": ["anemia of chronic kidney disease", "Anemia in chronic kidney disease", "Anaemia in chronic kidney disease", "anemia of chronic kidney disease (diagnosis)", "Anemia co-occurrent and due to chronic kidney disease", "Anaemia co-occurrent and due to chronic kidney disease", "Anemia co-occurrent and due to chronic kidney disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anemia in chronic kidney disease", "shortest_name_length": 32}
{"curie": "MONDO:0008487", "names": ["PCO", "PCOS", "PCO1", "PCOS1", "androgen excess", "Androgen Excess", "Androgen excess", "excess androgen", "Stein-Leventhal", "ovary polycystic", "polycystic ovary", "Polycystic ovary", "androgens excess", "androgen; excess", "Hyperandrogenism", "Hyperandrogenemia", "hyperandrogenemia", "polycystic; ovary", "excess; androgens", "HYPERANDROGENEMIA", "Polycystic ovaries", "polycystic ovaries", "Hyperandrogenaemia", "ovaries polycystic", "Sclerocystic Ovary", "multicystic ovaries", "Ovary, Sclerocystic", "Multicystic ovaries", "Sclerocystic ovaries", "Sclerocystic Ovaries", "Stein-Leventhal synd.", "ovarian hyperthecosis", "HYPERTHECOSIS, OVARIAN", "ANDROGEN EXCESS EFFECT", "Stein-Leventhal ovaries", "Cystic disease of ovary", "POLYCYSTIC OVARY DISEASE", "Stein-Leventhal syndrome", "Stein Leventhal Syndrome", "stein leventhal syndrome", "Polycystic ovary disease", "PCO - Polycystic ovaries", "stein-leventhal syndrome", "polycystic ovary disease", "Stein-Leventhal Syndrome", "Stein Leventhal syndrome", "STEIN LEVENTHAL SYNDROME", "STEIN-LEVENTHAL SYNDROME", "Increased androgen level", "increased androgen level", "disease ovary polycystic", "Stein Lenventhal syndrome", "Cystic disease of ovaries", "diseases ovary polycystic", "polycystic ovary disorder", "Polycystic ovary syndrome", "Syndrome, Stein-Leventhal", "polycystic ovary syndrome", "Polycystic Ovary Syndrome", "Polycystic Ovarian Disease", "OVARIAN POLYCYSTIC DISEASE", "polycystic; disease, ovary", "disease ovarian polycystic", "ovarian polycystic disease", "POYCYSTIC OVARIAN SYNDROME", "Ovary Syndrome, Polycystic", "Polycystic Ovarian disease", "Syndrome, Polycystic Ovary", "polycystic ovarian disease", "Polycystic ovarian disease", "Sclerocystic ovary syndrome", "Polycystic Ovarian Syndrome", "Polycystic Ovary Syndrome 1", "sclerocystic ovary syndrome", "polycystic ovarian syndrome", "Polycystic ovarian syndrome", "POLYCYSTIC OVARIAN SYNDROME", "syndrome; ovary, polycystic", "polycystic ovary syndrome 1", "ovary; syndrome, polycystic", "Sclerocystic Ovary Syndrome", "Polycystic ovary (disorder)", "POLYCYSTIC OVARY SYNDROME 1", "polycystic ovary (diagnosis)", "Ovarian Syndrome, Polycystic", "ovary; polycystic (syndrome)", "syndrome; polycystic ovarium", "syndrome; sclerocystic ovary", "SCLEROCYSTIC OVARIAN DISEASE", "sclerocystic ovarian disease", "ovary; syndrome, sclerocystic", "ovary; sclerocystic, syndrome", "syndrome; ovary, sclerocystic", "PCOS- polycystic ovary syndrome", "polycystic ovary syndrome (PCOS)", "PCOD - Polycystic ovarian disease", "Sclerocystic Ovarian Degeneration", "PCOS - Polycystic ovarian syndrome", "Ovarian Degeneration, Sclerocystic", "Polycystic Ovarian Syndrome (PCOS)", "PCOS (polycystic ovarian syndrome)", "Polycystic ovary syndrome (disorder)", "Androgen level above reference range", "BILATERAL POLYCYSTIC OVARIAN SYNDROME", "syndrome; bilateral polycystic ovarian", "bilateral polycystic ovarian; syndrome", "polycystic ovarian syndrome (diagnosis)", "disease (or disorder); ovary, polycystic", "disease (or disorder); polycystic, ovary", "increased androgen level (physical finding)", "Androgen level above reference range (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polycystic ovary syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0001557", "names": ["shoe boil", "Shoe boil", "Beat elbow", "Capped elbow", "capped elbow", "Miners' elbow", "Miner's elbow", "miner's elbow", "Elbow bursitis", "bursitis elbow", "elbow bursitis", "ELBOW, STUDENT", "miner's; elbow", "elbow; bursitis", "student's elbow", "Student's elbow", "bursitis; elbow", "BURSITIS OF ELBOW", "bursitis of elbow", "Bursitis of elbow", "olecranon bursitis", "bursitis olecranon", "Olecranon bursitis", "OLECRANON BURSITIS", "bursitis; olecranon", "olecranon; bursitis", "BURSITIS, OLECRANON", "bursitis of olecranon", "bursitis of elbow region", "Bursitis of elbow region", "elbow bursitis (& olecranon)", "Bursitis of elbow (disorder)", "bursitis of elbow (diagnosis)", "olecranon bursitis (diagnosis)", "Inflammation of bursa of olecranon", "Inflammation of bursa of olecranon (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "olecranon bursitis", "shortest_name_length": 9}
{"curie": "MONDO:0016376", "names": ["confetti-like macular atrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "confetti-like macular atrophy", "shortest_name_length": 29}
{"curie": "MONDO:0005617", "names": ["anaplastic carcinoma", "Anaplastic Carcinoma", "Carcinoma, anaplastic, NOS", "Undifferentiated carcinoma", "Undifferentiated Carcinoma", "carcinoma undifferentiated", "undifferentiated carcinoma", "carcinoma, undifferentiated", "Carcinoma, undifferentiated", "Undifferentiated Carcinomas", "Carcinoma, Undifferentiated", "Carcinoma, undifferentiated NOS", "Carcinoma, undifferentiated, NOS", "Carcinoma, undifferentiated type", "carcinoma, undifferentiated, malignant", "CARCINOMA, UNDIFFERENTIATED, MALIGNANT", "undifferentiated carcinoma (diagnosis)", "Carcinoma, undifferentiated (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "undifferentiated carcinoma", "shortest_name_length": 20}
{"curie": "MONDO:0016026", "names": ["infant epilepsy with migrant focal crisis", "epilepsy infant with migrant focal crisis", "Infant epilepsy with migrant focal crisis", "Infant epilepsy with migrant focal crisis (disorder)", "Infant epilepsy with migrant focal crisis (diagnosis)", "Early-onset progressive encephalopathy with migrant continuous myoclonus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infant epilepsy with migrant focal crisis", "shortest_name_length": 41}
{"curie": "MONDO:0017314", "names": ["EDS4", "vEDS", "EDS IV", "EDSVASC", "EDS type 4", "Vascular EDS", "vascular EDS", "Sack syndrome", "EDS4 (formerly)", "EDS IV (formerly)", "Vascular EDS (vEDS)", "EDS type 4 (formerly)", "Sack-Barabas syndrome", "sack-Barabas syndrome", "Arterial-ecchymotic EDS", "Ehlers-Danlos syndrome type 4", "type IV Ehlers-Danlos syndrome", "Ehlers-Danlos syndrome, type 4", "Type IV Ehlers-Danlos Syndrome", "Ehlers-Danlos syndrome type IV", "Type IV Ehlers Danlos Syndrome", "Ehlers-Danlos syndrome, type IV", "vascular Ehlers-Danlos syndrome", "Vascular Ehlers Danlos Syndrome", "Vascular Ehlers-Danlos syndrome", "Ehlers-Danlos Syndrome, Type IV", "Vascular Ehlers-Danlos Syndrome", "Ehlers-Danlos syndrome vascular", "Vascular Ehlers-Danlos Syndromes", "Syndrome, Vascular Ehlers-Danlos", "Ehlers-Danlos Syndrome, Vascular", "Ehlers-Danlos Syndromes, Vascular", "Syndromes, Vascular Ehlers-Danlos", "Vascular Type Ehlers-Danlos Syndrome", "Ehlers Danlos syndrome, arterial type", "Ehlers-Danlos syndrome, vascular type", "Ehlers-Danlos Syndrome, Arterial Type", "EHLERS-DANLOS SYNDROME, VASCULAR TYPE", "EHLERS-DANLOS SYNDROME, ARTERIAL TYPE", "Ehlers Danlos Syndrome, Arterial Type", "Ehlers-Danlos Syndrome, Vascular Type", "Ehlers Danlos Syndrome, Ecchymotic Type", "EHLERS-DANLOS SYNDROME, ECCHYMOTIC TYPE", "Ehlers Danlos syndrome, ecchymotic type", "Ehlers-Danlos Syndrome, Ecchymotic Type", "Ehlers-Danlos syndrome arterial type E-D", "Ehlers-Danlos syndrome type 4 (formerly)", "Ehlers-Danlos syndrome type IV (formerly)", "Ehlers-Danlos Syndrome, Sack-Barabas Type", "Ehlers Danlos syndrome, sack-Barabas type", "Ehlers-Danlos syndrome, type 4 (disorder)", "Ehlers Danlos Syndrome, Sack Barabas Type", "Ehlers Danlos Syndrome, Sack-Barabas Type", "EHLERS-DANLOS SYNDROME, SACK-BARABAS TYPE", "Ehlers-Danlos syndrome ecchymotic type E-D", "vascular Ehlers-Danlos syndrome (diagnosis)", "Ehlers-Danlos syndrome, type IV (diagnosis)", "Cutis hyperelastica IV, ecchymotic arterial type", "Ehlers Danlos Syndrome Type 4, Autosomal Dominant", "EHLERS-DANLOS SYNDROME, TYPE IV, AUTOSOMAL DOMINANT", "Ehlers-Danlos Syndrome, Type IV, Autosomal Dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ehlers-Danlos syndrome, vascular type", "shortest_name_length": 4}
{"curie": "MONDO:0008654", "names": ["NYS4", "SCA27A", "NYS4, FORMERLY", "SPINOCEREBELLAR ATAXIA 27A", "Nystagmus 4, congenital, autosomal dominant", "NYSTAGMUS 4, congenital, autosomal dominant", "nystagmus 4, congenital, autosomal dominant", "CEREBELLAR ATAXIA, AUTOSOMAL DOMINANT, FGF14-RELATED", "NYSTAGMUS 4, CONGENITAL, AUTOSOMAL DOMINANT, FORMERLY", "NYSTAGMUS 4, CONGENITAL, AUTOSOMAL DOMINANT (disorder)", "Vestibulocerebellar disorder with predominant ocular signs", "vestibulocerebellar disorder with predominant ocular signs", "VESTIBULOCEREBELLAR DISORDER WITH PREDOMINANT OCULAR SIGNS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nystagmus 4, congenital, autosomal dominant", "shortest_name_length": 4}
{"curie": "MONDO:0005756", "names": ["ETHMOIDITIS", "Ethmoiditis", "ethmoiditis", "ethmoid sinusitis", "ETHMOID SINUSITIS", "Ethmoid Sinusitis", "sinusitis ethmoid", "Sinusitis, Ethmoid", "Ethmoidal sinusitis", "Ethmoidal Sinusitis", "ethmoidal sinusitis", "Ethmoid Sinusitides", "ethmoidal; sinusitis", "Sinusitis, Ethmoidal", "sinusitis; ethmoidal", "Sinusitides, Ethmoid", "Ethmoidal Sinusitides", "Sinusitides, Ethmoidal", "ethmoid bone sinusitis", "Ethmoidal sinusitis NOS", "Ethmoidal sinusitis, NOS", "sinusitis of ethmoid bone", "Ethmoidal sinusitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ethmoid sinusitis", "shortest_name_length": 11}
{"curie": "MONDO:0018745", "names": ["superficial pemphigus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "superficial pemphigus", "shortest_name_length": 21}
{"curie": "MONDO:0017475", "names": ["Foot macrodactyly", "Macrodactyly of toe", "macrodactyly of foot", "Macrodactyly of foot", "macrodactyly of toes", "macrodactylia of toe", "Macrodactyly of toes", "Macrodactylia of toes", "Macrodactyly of the foot", "macrodactyly of the foot", "Megalodactyly of the foot", "megalodactylism of the foot", "Megalodactylism of the foot", "Macrodactyly of toe (disorder)", "macrodactylia of toe (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macrodactyly of toes", "shortest_name_length": 17}
{"curie": "MONDO:0001275", "names": ["Spinal meningioma", "meningioma spinal", "Spinal Meningioma", "spinal meningioma", "meningioma, spine", "Spinal Meningiomas", "Meningioma, Spinal", "Meningiomas, Spinal", "Spinal Cord Meningioma", "spinal cord meningioma", "cord meningioma spinal", "Spinal Cord meningioma", "meningioma of spinal cord", "Meningioma of Spinal Cord", "Meningioma of spinal cord", "Spinal meningioma (disorder)", "Meningioma of the Spinal Cord", "spinal meningioma (diagnosis)", "meningioma of the spinal cord", "spinal cord meningioma (disease)", "meningioma (disease) of spinal cord"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal meningioma", "shortest_name_length": 17}
{"curie": "UMLS:C4724970", "names": ["Metastatic Round Cell Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Round Cell Liposarcoma", "shortest_name_length": 33}
{"curie": "MONDO:0002022", "names": ["disorder of eye region", "orbital region disease", "eye and adnexa disease", "disease of orbital region", "ophthalmological disorder", "disorder of orbital region", "orbital region disease or disorder", "disease or disorder of orbital region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of orbital region", "shortest_name_length": 22}
{"curie": "MONDO:0006499", "names": ["hamartoma", "Hamartoma", "HAMARTOMA", "Hamartomas", "hamartomas", "HAMARTOMAS", "Hamartoma NOS", "Hamartomatous", "hamartomatous", "Hamartoma, NOS", "hamartoma (disease)", "Hamartoma (disorder)", "Hamartoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hamartoma", "shortest_name_length": 9}
{"curie": "MONDO:0100389", "names": ["AML, tri8", "AML, Trisomy 8", "Acute Myeloid Leukemia with tri8", "acute myeloid leukemia, Trisomy 8", "Acute Myeloid Leukemia with Trisomy 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, Trisomy 8", "shortest_name_length": 9}
{"curie": "MONDO:0002543", "names": ["Oligodendroglioma", "oligodendroglioma", "Adult Oligodendroglioma", "adult oligodendroglioma", "Brain Oligodendroglioma", "Oligodendroglioma, Adult", "oligodendroglioma, adult", "Adult Oligodendrogliomas", "Oligodendrogliomas, Adult", "oligodendroglioma of adults", "adult brain oligodendroglioma", "Adult Brain Oligodendroglioma", "brain tumor, oligodendroglioma", "CNS tumor, adult oligodendroglioma", "adult CNS tumor, oligodendroglioma", "CNS tumor, oligodendroglioma, adult", "Grade 2 Adult Oligodendroglial Tumor", "adult brain tumor, oligodendroglioma", "grade II adult oligodendroglial tumor", "Grade II Adult Oligodendroglial Tumor", "grade II adult Oligodendroglial tumor", "central nervous system tumor, oligodendroglioma, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult oligodendroglioma", "shortest_name_length": 17}
{"curie": "UMLS:C4525059", "names": ["Refractory Neuroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Neuroblastoma", "shortest_name_length": 24}
{"curie": "MONDO:0018874", "names": ["AML", "aml", "anll", "ANLL", "Acute Myeloid Leukemia", "Acute myeloid leukemia", "acute myeloid leukemia", "Acute myeloid leukaemia", "Myeloid leukemia, acute", "Leukemias acute myeloid", "Leukemia, Acute Myeloid", "Acute Myeloid Leukemias", "Myeloid Leukemia, Acute", "myeloid leukemia, acute", "Leukaemia;acute myeloid", "leukemia, acute myeloid", "acute myeloid leukaemia", "Leukemia, acute myeloid", "LEUKEMIA, ACUTE MYELOID", "acute myeloid leukemias", "Myeloid leukaemia, acute", "leukemia; myeloid, acute", "Leukemia, Myeloid, Acute", "Leukaemias acute myeloid", "Myeloid Leukemias, Acute", "LEUKEMIA, MYELOID, ACUTE", "Leukemias, Acute Myeloid", "myeloid; leukemia, acute", "acute myelocytic leukemia", "Acute Myelocytic Leukemia", "[M]Acute myeloid leukemia", "Acute myelocytic leukemia", "Acute myelocytic leukaemia", "[M]Acute myeloid leukaemia", "Acute Myeloid Leukemia NOS", "Leukemia, Acute Myelocytic", "ACUTE MYELOGENOUS LEUKEMIA", "Acute Myelocytic Leukemias", "Acute myeloid leukemia NOS", "Acute myelogenous leukemia", "Myelocytic Leukemia, Acute", "Acute Myelogenous Leukemia", "acute myelocytic leukaemia", "LEUKEMIA ACUTE MYELOGENOUS", "acute myelogenous leukemia", "Leukemia myeloblastic acute", "myelocytic; leukemia, acute", "Acute myeloid leukaemia NOS", "Acute granulocytic leukemia", "Acute Granulocytic Leukemia", "Myelogenous Leukemia, Acute", "Acute Myeloid Leukemia, NOS", "Leukemia, Acute Myelogenous", "LEUKEMIA, MYELOCYTIC, ACUTE", "Acute Myeloblastic Leukemia", "ACUTE MYELOBLASTIC LEUKEMIA", "Acute myelogenous leukaemia", "Leukemia, Myelocytic, acute", "Acute myeloblastic leukemia", "leukemia acute myeloblastic", "acute myeloblastic leukemia", "acute myelogenous leukemias", "LEUKEMIA, ACUTE MYELOGENOUS", "Myelocytic Leukemias, Acute", "Leukemias, Acute Myelocytic", "leukemia; myelocytic, acute", "Leukemia, Myelocytic, Acute", "acute granulocytic leukemia", "leukemia, acute myelogenous", "LEUKEMIA MYELOBLASTIC ACUTE", "acute myelogenous leukaemia", "Acute Myelogenous Leukemias", "LEUKEMIA ACUTE MYELOBLASTIC", "leukemia, myelocytic, acute", "Acute myeloid leukemia (AML)", "Acute Myeloid Leukemia (AML)", "Myeloblastic Leukemia, Acute", "Myelogenous Leukemias, Acute", "AML - Acute Myeloid Leukemia", "AML - Acute myeloid leukemia", "AML - acute Myeloid Leukemia", "acute myeloid leukemia (AML)", "Leukaemia myeloblastic acute", "Leukemia, Acute Myeloblastic", "LEUKEMIA, MYELOGENOUS, ACUTE", "Acute granulocytic leukaemia", "AML - acute myeloid leukemia", "Leukemia, Myelogenous, Acute", "Acute Myeloblastic Leukemias", "Leukemias, Acute Myelogenous", "acute myeloblastic leukaemia", "Acute myeloblastic leukaemia", "AML - Acute myeloid leukaemia", "Myeloblastic Leukemias, Acute", "granulocytic; leukemia, acute", "Leukemias, Acute Myeloblastic", "Acute Nonlymphocytic Leukemia", "acute nonlymphocytic leukemia", "LEUKEMIA, MYELOBLASTIC, ACUTE", "LEUKEMIA, GRANULOCYTIC, ACUTE", "Leukemia, Myeloblastic, Acute", "acute Nonlymphocytic leukemia", "leukemia; granulocytic, acute", "Leukemia, Acute Nonlymphocytic", "Acute Nonlymphocytic Leukemias", "leukemia, acute nonlymphocytic", "acute non-lymphocytic leukemia", "Nonlymphocytic Leukemia, Acute", "Acute non-lymphocytic leukemia", "Acute non-lymphocytic leukaemia", "Leukemias, Acute Nonlymphocytic", "acute nonlymphoblastic leukemia", "Acute myeloid leukemia, disease", "acute myeloid leukemia, somatic", "Nonlymphocytic Leukemias, Acute", "Acute myeloblastic leukemia NOS", "Leukemia, Nonlymphocytic, Acute", "Acute Nonlymphoblastic Leukemia", "Acute myelogenous leukemia (AML)", "Nonlymphoblastic Leukemia, Acute", "AML (acute myelogenous leukemia)", "acute non lymphoblastic leukemia", "Non-lymphoblastic leukemia acute", "Acute Nonlymphoblastic Leukemias", "Acute myeloid leukaemia, disease", "leukemia, acute myeloid, somatic", "Leukemia, Acute Nonlymphoblastic", "non-lymphoblastic leukemia acute", "acute myelogenous leukemia (AML)", "acute non-lymphoblastic leukemia", "Leukemias, Acute Nonlymphoblastic", "AML - Acute myeloblastic leukemia", "Nonlymphoblastic Leukemias, Acute", "Non-lymphoblastic leukaemia acute", "Leukemia, Nonlymphoblastic, Acute", "acute leukemias non lymphoblastic", "AML - Acute myeloblastic leukaemia", "acute nonlymphocytic leukemia (ANLL)", "acute myelogenous leukemia (diagnosis)", "acute myeloblastic leukemia (diagnosis)", "leukemia, acute myeloid, susceptibility to", "Acute myeloid leukemia, disease (disorder)", "LEUKEMIA, ACUTE MYELOID, SUSCEPTIBILITY TO", "Acute Myeloid Leukemia Not Otherwise Specified", "Acute myeloid leukemia (morphologic abnormality)", "hematopoeitic - acute Myleogenous leukemia (AML)", "Hematopoeitic - Acute Myleogenous Leukemia (AML)", "Acute Myeloid Leukemia Not Otherwise Categorized", "myeloid leukemia, acute, M4/M4Eo subtype, somatic", "Acute Myeloid Leukemia Defined by Differentiation", "leukemia, acute myeloid, reduced survival in, somatic", "leukemia, acute myeloid, autosomal dominant, somatic mutation", "leukemia, acute myeloid, susceptibility to, autosomal dominant, somatic mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia", "shortest_name_length": 3}
{"curie": "MONDO:0020068", "names": ["secondary encephalitis", "Postinfective encephalitis", "postinfectious encephalitis", "postinfectious; encephalitis", "encephalitis; postinfectious", "Post infectious encephalitis", "Post-infectious encephalitis", "postinfectious encephalitis (diagnosis)", "Post-infectious encephalitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postinfectious encephalitis", "shortest_name_length": 22}
{"curie": "UMLS:C4725089", "names": ["Refractory Human Papillomavirus-Related Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Human Papillomavirus-Related Malignant Neoplasm", "shortest_name_length": 58}
{"curie": "MONDO:0010981", "names": ["Holmes-Collins syndrome", "Holmes Collins syndrome", "tibia absent polydactyly arachnoid cyst", "Absent tibia-polydactyly-arachnoid cyst syndrome", "absent tibia-polydactyly-arachnoid cyst syndrome", "Absent tibia, polydactyly, arachnoid cyst syndrome", "Absent tibia, polydactyly, arachnoid cyst syndrome (disorder)", "absence/hypoplasia of tibia, polydactyly, retrocerebellar arachnoid cyst, and other anomalies", "Tibia, Absence or Hypoplasia of, with Polydactyly, Retrocerebellar Arachnoid Cyst, and Other Anomalies", "tibia, absence or hypoplasia of, with polydactyly, retrocerebellar arachnoid cyst, and other anomalies", "tibia, absence or hypoplasia of, with polydactyly, RETROCEREBELLAR arachnoid cyst, and other anomalies", "TIBIA, ABSENCE OR HYPOPLASIA OF, WITH POLYDACTYLY, RETROCEREBELLAR ARACHNOID CYST, AND OTHER ANOMALIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "absent tibia-polydactyly-arachnoid cyst syndrome", "shortest_name_length": 23}
{"curie": "UMLS:C5419772", "names": ["Small Intestinal Neuroendocrine Tumor G3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Intestinal Neuroendocrine Tumor G3", "shortest_name_length": 40}
{"curie": "UMLS:C5420273", "names": ["Oropharyngeal Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oropharyngeal Lymphoma", "shortest_name_length": 22}
{"curie": "MONDO:0016941", "names": ["partial trisomy of chromosome 4p", "partial duplication of chromosome 4p", "partial trisomy of the short arm of chromosome 4", "partial duplication of the short arm of chromosome 4", "partial duplication of the short arm of chromosome type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of the short arm of chromosome 4", "shortest_name_length": 32}
{"curie": "UMLS:C1332489", "names": ["Benign Dermal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Dermal Neoplasm", "shortest_name_length": 22}
{"curie": "MONDO:0016554", "names": ["neonatal iodine exposure", "iodine antenatal exposure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal iodine exposure", "shortest_name_length": 24}
{"curie": "MONDO:0003615", "names": ["nerve trap", "trap nerve", "Trapped nerve", "trapped nerve", "Entrapment syndrome", "entrapment neuropathy", "neuropathy entrapment", "Entrapment neuropathy", "Entrapment Neuropathy", "neuropathy; entrapment", "compression neuropathy", "Neuropathy, Entrapment", "Compression neuropathy", "Entrapment Neuropathies", "Entrapment neuropathies", "entrapment neuropathies", "Entrapment syndrome, NOS", "Neuropathies, Entrapment", "compression neuropathies", "NERVE ENTRAPMENT SYNDROME", "nerve entrapment syndrome", "Nerve entrapment syndrome", "nerve compression syndrome", "Nerve compression syndrome", "Entrapment neuropathy, NOS", "Nerve Compression Syndrome", "Nerve entrapment syndromes", "Nerve Compression Syndromes", "Compression Syndrome, Nerve", "Syndrome, Nerve Compression", "nerve compression syndromes", "Compression Syndromes, Nerve", "Syndromes, Nerve Compression", "peripheral nerve entrapment syndrome", "Peripheral nerve entrapment syndrome", "Peripheral nerve entrapment syndrome (disorder)", "peripheral nerve entrapment syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nerve compression syndrome", "shortest_name_length": 10}
{"curie": "UMLS:C0021139", "names": ["Inadequate Personality", "Inadequate personality", "INADEQUATE PERSONALITY", "inadequate personality", "Personality;inadequate", "inadequate; personality", "Personality, Inadequate", "personality; inadequate", "personality disorder; inadequate", "inadequate; personality disorder", "Inadequate personality (finding)", "Inadequate personality (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Inadequate Personality", "shortest_name_length": 22}
{"curie": "UMLS:C4763785", "names": ["Recurrent Primary Bone Lymphoma", "Recurrent Primary Lymphoma of Bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Primary Bone Lymphoma", "shortest_name_length": 31}
{"curie": "MONDO:0024298", "names": ["avitaminoses", "avitaminosis", "AVITAMINOSIS", "Avitaminoses", "Avitaminosis", "HYPOVITAMINOSIS", "Hypovitaminosis", "hypovitaminosis", "lack of vitamins", "Avitaminosis, NOS", "VITAMIN DEFICIENCY", "Deficiency;vitamin", "Vitamin Deficiency", "Deficiency vitamin", "DEFICIENCY VITAMIN", "Vitamin deficiency", "vitamin deficiency", "deficiency, vitamin", "vitamin; deficiency", "Hypovitaminosis NOS", "deficiency; vitamin", "Deficiency, Vitamin", "Vitamin Deficiencies", "Hypovitaminosis, NOS", "vitamin deficiencies", "deficiencies, vitamin", "Deficiencies, Vitamin", "Vitamin deficiency NOS", "Vitamin deficiency, NOS", "vitamin deficiency disorder", "vitamin deficiency syndrome", "Vitamin Deficiency Disorder", "AVITAMINOSIS A B B1 B2 ETC.", "Vitamin Deficiency Disorders", "Vitamin deficiency (disorder)", "Unspecified vitamin deficiency", "vitamin deficiency (diagnosis)", "Vitamin deficiency, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitamin deficiency disorder", "shortest_name_length": 12}
{"curie": "MONDO:0011352", "names": ["neuroendocrine carcinoma of salivary glands, sensorineural hearing loss, and enamel hypoplasia", "NEUROENDOCRINE CARCINOMA OF SALIVARY GLANDS, SENSORINEURAL HEARING LOSS, AND ENAMEL HYPOPLASIA", "Neuroendocrine Carcinoma of Salivary Glands, Sensorineural Hearing Loss, and Enamel Hypoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuroendocrine carcinoma of salivary glands, sensorineural hearing loss, and enamel hypoplasia", "shortest_name_length": 94}
{"curie": "MONDO:0000634", "names": ["benign thoracic tumor", "Benign Thoracic Tumor", "Benign Tumor of Thorax", "benign tumor of thorax", "Benign tumor of thorax", "Benign tumour of thorax", "thoracic benign neoplasm", "benign thoracic neoplasm", "Benign Thoracic Neoplasm", "benign neoplasm of thorax", "Benign Neoplasm of Thorax", "Benign neoplasm of thorax", "Benign Tumor of the Thorax", "benign tumor of the thorax", "Thoracic benign neoplasm NOS", "benign neoplasm of the thorax", "Benign Neoplasm of the Thorax", "Benign neoplasm of thorax (disorder)", "benign neoplasm of thorax (diagnosis)", "thoracic segment of trunk benign neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thoracic benign neoplasm", "shortest_name_length": 21}
{"curie": "UMLS:C0277986", "names": ["Edema gum", "Oedema gum", "Gingival edema", "Gingival oedema", "Edema of gingiva", "Gingival edema (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gingival edema", "shortest_name_length": 9}
{"curie": "UMLS:C1336961", "names": ["Very Low Risk Small Intestinal Gastrointestinal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Very Low Risk Small Intestinal Gastrointestinal Stromal Tumor", "shortest_name_length": 61}
{"curie": "UMLS:C5238803", "names": ["Glycogen storage disorder", "Myopathy Secondary to Glycogen Storage Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myopathy Secondary to Glycogen Storage Disorder", "shortest_name_length": 25}
{"curie": "MONDO:0015716", "names": ["moderately severe hemophilia B", "moderately severe hemophilia type B", "moderately severe factor IX deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "moderately severe hemophilia B", "shortest_name_length": 30}
{"curie": "MONDO:0009560", "names": ["MOTA", "MOTA syndrome", "MARLES SYNDROME", "Marles syndrome", "Oculotrichoanal syndrome", "oculotrichoanal syndrome", "Manitoba Trichoanal syndrome", "Marles-Greenberg-Persaud Syndrome", "MANITOBA OCULOTRICHOANAL SYNDROME", "MANITOBA oculotrichoanal syndrome", "Marles-Greenberg-Persaud syndrome", "Manitoba Oculotrichoanal Syndrome", "Manitoba oculotrichoanal syndrome", "Marles-Greenburg-Persaud syndrome", "Marles Greenberg Persaud syndrome", "MOTA - Manitoba oculotrichoanal syndrome", "Manitoba oculotrichoanal syndrome (disorder)", "unilateral upper eyelid coloboma, aberrant anterior hairline pattern, and anal anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculotrichoanal syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0030731", "names": ["AAT12", "AORTIC ANEURYSM, FAMILIAL THORACIC 12", "aortic aneurysm, familial thoracic 12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic aneurysm, familial thoracic 12", "shortest_name_length": 5}
{"curie": "MONDO:0005371", "names": ["Mood disorder", "Mood Disorder", "mood disorder", "MOOD DISORDER", "disorder mood", "MOOD DISORDERS", "mood disorders", "Disorder, Mood", "Mood disorders", "Mood Disorders", "disorders mood", "affect disorder", "Disorders, Mood", "disorder affect", "affects disorder", "affect disorders", "Mood disorder NOS", "affecive disorder", "mood disorder nos", "Affective disorder", "Disorder;affective", "Mood disorder, NOS", "affective disorder", "Disorder of affect", "Affective Disorder", "AFFECTIVE DISORDER", "Affective disorders", "affective; disorder", "Affective Disorders", "affective disorders", "disorder; affective", "Disorder, Affective", "Disorders, Affective", "affecive disorder nos", "episodic mood disorder", "AFFECTIVE DISORDER NOS", "Affective disorder NOS", "Affective Disturbances", "Disorder of affect, NOS", "Affective disorders NOS", "Mood disorder (disorder)", "affective mood disorders", "mood disorder (diagnosis)", "psychiatric disorders mood", "UNSPECIFIED MOOD DISORDERS", "Mood [affective] disorders", "Mood [affective] disorders (F30-F39)", "Unspecified mood [affective] disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mood disorder", "shortest_name_length": 13}
{"curie": "MONDO:0006312", "names": ["myofibroma", "Myofibroma", "Myofibromas", "Lipoleiomyoma", "lipoleiomyoma", "Solitary Myofibromatosis", "infantile hemangiopericytoma", "myofibroma (morphologic abnormality)", "Myofibroma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myofibroma", "shortest_name_length": 10}
{"curie": "MONDO:0010751", "names": ["UNIQUE GREEN PHENOMENON", "unique green phenomenon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "unique green phenomenon", "shortest_name_length": 23}
{"curie": "MONDO:0019125", "names": ["PANCHONDRITIS", "Jaksch' syndrome", "Polychondropathia", "Ashkenazi syndrome", "Meyenburg's disease", "Chronic polychondritis", "chronic polychondritis", "Systemic chondromalacia", "Relapsing Polychondritis", "RELAPSING POLYCHONDRITIS", "relapsing polychondritis", "polychondritis relapsing", "CHONDROMALACIA, SYSTEMIC", "chondromalacia, systemic", "POLYCHONDRITIS RELAPSING", "recurrent polychondritis", "Chondromalacia, systemic", "Relapsing polychondritis", "Polychondritis, relapsing", "POLYCHONDRITIS, RELAPSING", "Polychondritis, Relapsing", "Relapsing Polychondritides", "Polychondritides, Relapsing", "Jaksch Wartenhorst's syndrome", "Chronic Atrophic Polychondritis", "chronic atrophic polychondritis", "Chronic atrophic polychondritis", "Atrophic Polychondritis, Chronic", "Polychondritis, Chronic Atrophic", "POLYCHONDRITIS, CHRONIC ATROPHIC", "Chronic Atrophic Polychondritides", "Von Jaksch Wartenhorst's syndrome", "Polychondritides, Chronic Atrophic", "Atrophic Polychondritides, Chronic", "Myenberg-Altherr-Uehlinger syndrome", "Relapsing polychondritis (disorder)", "Meyenburg-Altherr-Uehlinger syndrome", "relapsing polychondritis (diagnosis)", "recrudescent [Brill-Zinsser]; polychondritis", "polychondritis; recrudescent [Brill-Zinsser]", "Atrophic polychondritis, cartilagenous arthritic deafness syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "relapsing polychondritis", "shortest_name_length": 13}
{"curie": "UMLS:C5446393", "names": ["Lacrimal Gland Myoepithelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lacrimal Gland Myoepithelioma", "shortest_name_length": 29}
{"curie": "UMLS:C0340770", "names": ["vein injury", "injury veins", "injury; vein", "vein; injury", "Venous Injury", "Venous injury", "injuries vein", "Injury of vein", "Venous injury, NOS", "Injury of vein, NOS", "Injury of vein (disorder)", "Venous injury (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Venous Injury", "shortest_name_length": 11}
{"curie": "MONDO:0003776", "names": ["Renal Pelvis Inverted Papilloma", "renal pelvis inverted papilloma", "Kidney Pelvis Inverted Papilloma", "kidney pelvis inverted papilloma", "Inverted Papilloma of Renal Pelvis", "inverted papilloma of renal pelvis", "inverted papilloma of kidney pelvis", "Inverted Papilloma of Kidney Pelvis", "Inverted Papilloma of the Renal Pelvis", "inverted papilloma of the renal pelvis", "inverted papilloma of the kidney pelvis", "Inverted papilloma of the kidney Pelvis", "Inverted Papilloma of the Kidney Pelvis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal pelvis inverted papilloma", "shortest_name_length": 31}
{"curie": "MONDO:0700020", "names": ["chromosome 13 disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 13 disorder", "shortest_name_length": 22}
{"curie": "UMLS:C5446670", "names": ["Refractory Desmoid Fibromatosis", "Refractory Desmoid-Type Fibromatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Desmoid Fibromatosis", "shortest_name_length": 31}
{"curie": "MONDO:0002203", "names": ["Dyschezia", "dyschesia", "Dyschesia", "dyschezia", "constipate", "Constipated", "constipated", "Costiveness", "constipating", "Constipation", "constipation", "CONSTIPATION", "colonic inertia", "defecation pain", "pain defecation", "DEFECATION PAIN", "fecal; retention", "Pain;defaecation", "retention; fecal", "RNDx constipation", "CN - Constipation", "painful defecation", "Painful defecation", "Defecation painful", "pain on defecation", "pain on defaecation", "Defaecation painful", "Painful defaecation", "Pain with defecation", "Bowel action painful", "constipation disorder", "difficulty defecating", "Difficulty defecating", "constipation (symptom)", "Constipation (finding)", "Difficulty defaecating", "Difficult passing motion", "Difficulty passing stool", "constipation (diagnosis)", "Unspecified Constipation", "Difficulty opening bowels", "Constipation, unspecified", "RNDx unspecified constipation", "RNDx constipation (diagnosis)", "Pain associated with defecation", "Pain associated with defaecation", "Pain associated with defecation (finding)", "RNDx unspecified constipation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "constipation disorder", "shortest_name_length": 9}
{"curie": "UMLS:C0232058", "names": ["apnea newborn", "newborn apnea", "apnea; newborn", "apnea neonatal", "Neonatal apnea", "APNEA NEONATAL", "neonatal apnea", "newborn; apnea", "Apnea neonatal", "APNOEA NEONATAL", "Neonatal apnoea", "Apnoea neonatal", "Apnea, neonatal", "Apnea neonatorum", "Apnea in newborn", "Apnea of newborn", "Apnoea in newborn", "Apnoea of newborn", "Apnoea neonatorum", "Apnea in the newborn", "apnea in the newborn", "Apnea of newborn, NOS", "Apnoea in the newborn", "newborn apnea (diagnosis)", "Apnea in newborn (finding)", "Unspecified apnea of newborn"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Apnea in newborn", "shortest_name_length": 13}
{"curie": "UMLS:C5420407", "names": ["Maxillofacial Mesenchymal Chondrosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Maxillofacial Mesenchymal Chondrosarcoma", "shortest_name_length": 40}
{"curie": "MONDO:0020393", "names": ["discrete fibromuscular subaortic stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "discrete fibromuscular subaortic stenosis", "shortest_name_length": 41}
{"curie": "UMLS:C4524844", "names": ["Small Intestinal Cancer by AJCC v7 Stage", "Small Intestinal Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Intestinal Cancer by AJCC v7 Stage", "shortest_name_length": 40}
{"curie": "MONDO:0007410", "names": ["CRYPTOP", "ANKYLOBLEPHARON, SIMPLE", "Ankyloblepharon, Simple", "ankyloblepharon, simple", "Isolated cryptophthalmia", "Isolated cryptophthalmos", "isolated cryptophthalmia", "nonsyndromic cryptophthalmia", "Isolated cryptophthalmos (disorder)", "unilateral or bilateral isolated cryptophthalmos", "Cryptophthalmos, Unilateral or Bilateral, Isolated", "cryptophthalmos, unilateral or bilateral, isolated", "CRYPTOPHTHALMOS, UNILATERAL OR BILATERAL, ISOLATED", "Cryptophthalmos with Microphthalmia and Peters Anomaly", "CRYPTOPHTHALMOS WITH MICROPHTHALMIA AND PETERS ANOMALY", "cryptophthalmos with microphthalmia and Peters anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated cryptophthalmia", "shortest_name_length": 7}
{"curie": "UMLS:C1708669", "names": ["Leaflet Disruption Due To Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leaflet Disruption Due To Infection", "shortest_name_length": 35}
{"curie": "UMLS:C4521877", "names": ["Stage IIB", "Stage IIB Pancreatic Cancer", "Stage IIB Pancreatic Cancer AJCC v8", "Stage IIB Exocrine Pancreatic Cancer AJCC v8", "Stage IIB Exocrine Pancreatic Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Pancreatic Cancer AJCC v8", "shortest_name_length": 9}
{"curie": "MONDO:0044878", "names": ["Germ Cell Tumor", "germ cell tumor", "adult germ cell tumor", "Adult germ cell tumor", "Adult Germ Cell Tumor", "germ cell tumor of adults"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult germ cell tumor", "shortest_name_length": 15}
{"curie": "UMLS:C5671043", "names": ["Refractory Epstein-Barr Virus-Related Lymphoproliferative Disease with Primary Immunodeficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Epstein-Barr Virus-Related Lymphoproliferative Disease with Primary Immunodeficiency", "shortest_name_length": 95}
{"curie": "MONDO:0010968", "names": ["GLC3B", "GLC3 type B", "Glc3, type B", "GLC3, TYPE B", "primary congenital glaucoma", "glaucoma 3 primary infantile B", "GLAUCOMA 3, PRIMARY INFANTILE, B", "Glaucoma 3, primary infantile, B", "glaucoma 3, primary infantile, B", "glaucoma primary congenita type 3B", "primary congenital glaucoma type 3B", "Primary congenital glaucoma type 3B", "GLAUCOMA, PRIMARY CONGENITAL, TYPE B", "glaucoma, primary congenital, type B", "Glaucoma, Primary Congenital, Type B", "Glaucoma, primary congenital, type 3B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glaucoma 3, primary infantile, B", "shortest_name_length": 5}
{"curie": "UMLS:C4688618", "names": ["p16INK4a Negative Oropharyngeal Squamous Cell Cancer", "p16INK4a Negative Oropharyngeal Squamous Cell Carcinoma", "Oropharyngeal p16INK4a-Negative Squamous Cell Carcinoma", "Oropharyngeal Squamous Cell Carcinoma, p16INK4a Negative"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oropharyngeal p16INK4a-Negative Squamous Cell Carcinoma", "shortest_name_length": 52}
{"curie": "UMLS:C0349527", "names": ["Skin Fibrous Tissue Tumor", "Cutaneous Fibrocytic Tumor", "Skin Fibroblastic Neoplasm", "Skin Fibrous Tissue Neoplasm", "Cutaneous Fibroblastic Tumor", "Fibrous tissue tumor of skin", "Fibrous tissue tumour of skin", "Cutaneous Fibrocytic Neoplasm", "Cutaneous fibrous tissue tumor", "Cutaneous Fibrous Tissue Tumor", "Cutaneous fibrous tissue tumour", "Cutaneous Fibroblastic Neoplasm", "Fibrous tissue neoplasm of skin", "Cutaneous Fibrous Tissue Neoplasm", "Fibrous tissue neoplasm of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fibrous tissue neoplasm of skin", "shortest_name_length": 25}
{"curie": "UMLS:C0007852", "names": ["Cervical migraine syndrome", "Cervical Migraine Syndrome", "Migraine Syndrome, Cervical", "Cervical Migraine Syndromes", "Migraine Syndromes, Cervical"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Migraine Syndrome", "shortest_name_length": 26}
{"curie": "UMLS:C2315425", "names": ["Peritoneal Dialysis Catheter Infection", "Infection of peritoneal dialysis catheter", "Infection of peritoneal dialysis catheter (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infection of peritoneal dialysis catheter", "shortest_name_length": 38}
{"curie": "UMLS:C0276824", "names": ["Meningoencephalitis due to Naegleria", "Meningoencephalitis caused by Naegleria", "Meningoencephalitis caused by Naegleria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meningoencephalitis due to Naegleria", "shortest_name_length": 36}
{"curie": "MONDO:0021979", "names": ["Basaran Yilmaz syndrome", "keratoderma, hypotrichosis and leukonychia totalis", "Keratoderma, hypotrichosis and leukonychia totalis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Basaran Yilmaz syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0011832", "names": ["DFNA44", "autosomal dominant deafness 44", "Deafness, Autosomal Dominant 44", "DEAFNESS, AUTOSOMAL DOMINANT 44", "deafness, autosomal dominant 44", "deafness, autosomal dominant type 44", "autosomal dominant nonsyndromic deafness 44", "autosomal dominant nonsyndromic hearing loss 44", "CCDC50 autosomal dominant nonsyndromic deafness", "autosomal dominant nonsyndromic deafness type 44", "autosomal dominant nonsyndromic deafness caused by mutation in CCDC50"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 44", "shortest_name_length": 6}
{"curie": "MONDO:0015661", "names": ["dextrocardia", "DEXTROCARDIA", "Dextrocardia", "Dextrocardias", "right sided heart", "Right sided heart", "Heart in right chest", "HEART DEXTROPOSITION", "dextrocardia (disease)", "Thoracic situs inversus", "Dextrocardia (disorder)", "dextrocardia (diagnosis)", "heart predominantly in right hemithorax", "Heart predominantly in right hemithorax", "malposition; congenital, heart, dextrocardia", "heart; malposition, congenital, dextrocardia", "Heart tip and four chambers point towards right side of body"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dextrocardia", "shortest_name_length": 12}
{"curie": "MONDO:0012441", "names": ["Mgr11", "MGR11", "migraine with or without aura, susceptibility to, 11", "MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 11", "migraine with or without aura, susceptibility to, type 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "migraine with or without aura, susceptibility to, 11", "shortest_name_length": 5}
{"curie": "UMLS:C5668247", "names": ["Unresectable Sarcomatoid Renal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Sarcomatoid Renal Cell Carcinoma", "shortest_name_length": 45}
{"curie": "UMLS:C4520919", "names": ["stage I endometrial cancer", "stage I cancer of the uterus", "Stage I Endometrial Cancer AJCC v6", "Stage I Uterine Corpus Cancer AJCC v6", "Stage I Cancer of Uterine Corpus AJCC v6", "Stage I Cancer of the Corpus Uteri AJCC v6", "Stage I Cancer of the Uterine Corpus AJCC v6", "Stage I Uterine (including Endometrial) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Uterine Corpus Cancer AJCC v6", "shortest_name_length": 26}
{"curie": "UMLS:C0476159", "names": ["Physeal fracture", "Epiphyseal fracture", "Epiphyseal Fracture", "epiphyseal fracture", "epiphyseal fractures", "Fracture of bone involving growth plate", "Fractures involving the epiphyseal plate", "[Q] Fractures involving the epiphyseal plate", "Fracture of bone involving growth plate (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fracture of bone involving growth plate", "shortest_name_length": 16}
{"curie": "MONDO:0010081", "names": ["subaortic stenosis, membranous", "Subaortic Stenosis, Membranous", "SUBAORTIC STENOSIS, MEMBRANOUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subaortic stenosis, membranous", "shortest_name_length": 30}
{"curie": "MONDO:0006847", "names": ["malignant lymphatic vessel tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant lymphatic vessel tumor", "shortest_name_length": 32}
{"curie": "MONDO:0007757", "names": ["HYPERKERATOSIS-HYPERPIGMENTATION SYNDROME", "Hyperkeratosis-Hyperpigmentation Syndrome", "Hyperkeratosis-hyperpigmentation syndrome", "hyperkeratosis-hyperpigmentation syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperkeratosis-hyperpigmentation syndrome", "shortest_name_length": 41}
{"curie": "MONDO:0001449", "names": ["lcm", "LCM", "Armstrong Syndrome", "Syndrome, Armstrong", "Armstrong's disease", "LCM virus infection", "Armstrong's Syndrome", "Syndrome, Armstrong's", "meningitis lymphocytic", "Meningitis;lymphocytic", "Lymphocytic Meningitis", "lymphocytic meningitis", "Lymphocytic meningitis", "lymphocytic choriomeningitis", "Choriomeningitis lymphocytic", "Lymphocytic choriomeningitis", "Lymphocytic Choriomeningitis", "Choriomeningitis, Lymphocytic", "CHORIOMENINGITIS, LYMPHOCYTIC", "MENINGITIS, LYMPHOCYTIC BENIGN", "Lymphocytic meningoencephalitis", "lymphocytic meningoencephalitis", "Lymphocytic meningitis (disorder)", "LCM - Lymphocytic choriomeningitis", "MENINGITIS LYMPHOCYTIC CHORIOMENINGITIS", "Lymphocytic choriomeningitis (disorder)", "lymphocytic choriomeningitis (diagnosis)", "Lymphocytic meningoencephalitis (disorder)", "Lymphocytic choriomeningitis virus infection", "Lymphocytic choriomeningitis virus encephalomyelitis", "Meningitis due to lymphocytic choriomeningitis virus", "lymphocytic choriomeningitis virus encephalomyelitis", "Lymphocytic Choriomeningitis Virus Encephalomyelitis", "Encephalomyelitis, Lymphocytic Choriomeningitis Virus", "Infection caused by Lymphocytic choriomeningitis virus", "Encephalomyelitis caused by lymphocytic choriomeningitis virus", "Infection caused by Lymphocytic choriomeningitis virus (disorder)", "lymphocytic choriomeningitis mammarenavirus infectious meningitis", "lymphocytic choriomeningitis mammarenavirus caused infectious meningitis", "Encephalomyelitis caused by lymphocytic choriomeningitis virus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphocytic choriomeningitis", "shortest_name_length": 3}
{"curie": "MONDO:0024982", "names": ["animal Salmonella infection", "Animal Salmonella Infection", "infection, animal Salmonella", "Infection, Animal Salmonella", "Salmonella Infection, Animal", "Salmonella infection, animal", "Animal Salmonella Infections", "animal Salmonella infections", "Infections, Animal Salmonella", "salmonella infections, animal", "Salmonella Infections, Animal", "infections, animal Salmonella", "salmonellosis, non-human animal", "Salmonella infections in animals"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "salmonella infections, animal", "shortest_name_length": 27}
{"curie": "MONDO:0006526", "names": ["allergic urticaria", "Allergic urticaria", "urticaria; allergic", "URTICARIA, ALLERGIC", "allergic; urticaria", "allergic form of urticaria", "allergic urticaria (disease)", "Allergic urticaria (disorder)", "allergic urticaria (diagnosis)", "allergic form of urticaria (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "allergic urticaria", "shortest_name_length": 18}
{"curie": "UMLS:C0687675", "names": ["loss pregnancy", "pregnancy loss", "Pregnancy loss", "Pregnancy Loss", "losses pregnancy", "pregnancy loss (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pregnancy loss", "shortest_name_length": 14}
{"curie": "MONDO:0100487", "names": ["TPM4-related platelet disorder", "TPM4-related platelet dysfunction with or without thrombocytopenia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "TPM4-related platelet disorder", "shortest_name_length": 30}
{"curie": "MONDO:0003254", "names": ["heart granular cell tumor", "Heart Granular Cell Tumor", "Cardiac granular cell tumor", "Cardiac Granular Cell Tumor", "Granular Cell Tumor of Heart", "granular cell tumor of Heart", "granular cell tumor of heart", "Cardiac granular cell neoplasm", "cardiac granular cell neoplasm", "Cardiac Granular Cell Neoplasm", "granular cell neoplasm of heart", "Granular Cell Neoplasm of Heart", "granular cell tumor of the heart", "Granular Cell Tumor of the Heart", "granular cell neoplasm of the heart", "Granular Cell Neoplasm of the Heart"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiac granular cell neoplasm", "shortest_name_length": 25}
{"curie": "MONDO:0003272", "names": ["mixed epithelial stromal tumor", "mixed epithelial stromal tumour"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed epithelial stromal tumor", "shortest_name_length": 30}
{"curie": "MONDO:0013365", "names": ["DFNB83", "autosomal recessive deafness 83", "deafness, autosomal recessive 83", "DEAFNESS, AUTOSOMAL RECESSIVE 83", "autosomal recessive nonsyndromic deafness 83", "autosomal recessive nonsyndromic hearing loss 83", "autosomal recessive nonsyndromic deafness type 83"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 83", "shortest_name_length": 6}
{"curie": "MONDO:0010182", "names": ["HYPERCAROTENEMIA AND VITAMIN A DEFICIENCY, AUTOSOMAL RECESSIVE", "Hypercarotenemia And Vitamin A Deficiency, Autosomal Recessive", "hypercarotenemia and vitamin A deficiency, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypercarotenemia and vitamin A deficiency, autosomal recessive", "shortest_name_length": 62}
{"curie": "MONDO:0014492", "names": ["PPKWH", "KWWH type IV", "Keratoderma with wooly hair type IV", "keratoderma with woolly hair type IV", "Keratoderma with woolly hair type IV", "palmoplantar keratoderma and woolly hair", "PALMOPLANTAR KERATODERMA AND WOOLLY HAIR", "Woolly hair-palmoplantar keratoderma syndrome", "woolly hair-palmoplantar keratoderma syndrome", "woolly hair-palmoplantar hyperkeratosis syndrome", "Woolly hair-palmoplantar hyperkeratosis syndrome", "Wooly hair with palmoplantar keratoderma syndrome", "Woolly hair with palmoplantar keratoderma syndrome", "Wooly hair with palmoplantar keratoderma syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "woolly hair-palmoplantar keratoderma syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0001727", "names": ["cochleovestibular active Mnire's disease", "Cochleovestibular active Mnire's disease", "active cochleovestibular Meniere disease", "Active cochleovestibular Ménière disease", "Cochleovestibular active Meniere's disease", "Active cochleovestibular Ménière's disease", "active cochleovestibular Meniere's disease", "Active cochleovestibular Meniere's disease", "Active Meniere's disease, cochleovestibular", "Active Ménière's disease, cochleovestibular", "active Meniere's disease, cochleovestibular", "Active cochleovestibular Ménière's disease (disorder)", "active cochleovestibular Meniere's disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "active cochleovestibular Meniere disease", "shortest_name_length": 40}
{"curie": "UMLS:C0034219", "names": ["Alveolar pyorrhea", "Alveolar pyorrhoea", "pyorrhea alveolaris", "Pyorrhea alveolaris", "Pyorrhea Alveolaris", "Pyorrhoea alveolaris", "Alveolar pyorrhea (disorder)", "pyorrhea alveolaris (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alveolar pyorrhea", "shortest_name_length": 17}
{"curie": "MONDO:0011891", "names": ["FEB8", "ECA2", "GEFS+3", "GEFSP3", "GEFS, Type 3", "GEFS+, TYPE 3", "Gefs+, type 3", "familial febrile seizures 8", "FEBRILE SEIZURES, FAMILIAL, 8", "febrile seizures, familial, 8", "familial febrile convulsions 8", "FEBRILE CONVULSIONS, FAMILIAL, 8", "Febrile Convulsions, Familial, 8", "GABRG2 childhood absence epilepsy", "susceptibility to childhood absence epilepsy 2", "EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2", "epilepsy, childhood absence, susceptibility to, 2", "GABRG2 generalized epilepsy with febrile seizures plus", "epilepsy, childhood absence, susceptibility to, type 2", "generalized epilepsy with febrile seizures plus, type 3", "GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 3", "Generalized Epilepsy With Febrile Seizures Plus, Type 3", "childhood absence epilepsy caused by mutation in GABRG2", "generalized epilepsy with febrile seizures plus caused by mutation in GABRG2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "febrile seizures, familial, 8", "shortest_name_length": 4}
{"curie": "UMLS:C0151512", "names": ["ATROPHY INJECTION SITE", "Atrophy injection site", "Injection site atrophy", "INJECTION SITE ATROPHY", "Injection site atrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site atrophy", "shortest_name_length": 22}
{"curie": "UMLS:C5237037", "names": ["Recurrent Fallopian Tube Endometrioid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Fallopian Tube Endometrioid Adenocarcinoma", "shortest_name_length": 52}
{"curie": "MONDO:0019550", "names": ["HMSN with acrodystrophy", "AR-CMT2 with acrodystrophy", "hereditary motor and sensory neuropathy with acrodystrophy", "autosomal recessive Charcot-Marie-Tooth type 2 with acrodystrophy", "autosomal recessive axonal Charcot-Marie-Tooth disease with acrodystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary motor and sensory neuropathy with acrodystrophy", "shortest_name_length": 23}
{"curie": "MONDO:0010138", "names": ["GRD", "GRD1", "thyrotoxicosis", "THYROTOXICOSIS", "toxic; thyroid", "thyroid; toxic", "Thyrotoxicoses", "Thyrotoxicosis", "Thyrotoxicosis NOS", "Thyrotoxicosis, NOS", "Thyrotoxicosis (disorder)", "thyrotoxicosis (diagnosis)", "Thyrotoxicosis, unspecified", "hyperthyroidism, autoimmune", "Graves disease, susceptibility to, 1", "Thyrotoxicosis with or without goitre", "Thyrotoxicosis with or without goiter", "Thyrotoxicosis with or without goiter (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyrotoxicosis", "shortest_name_length": 3}
{"curie": "UMLS:C1707985", "names": ["Extracardiac Rhabdomyoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extracardiac Rhabdomyoma", "shortest_name_length": 24}
{"curie": "MONDO:0009601", "names": ["MDWH", "CHHV", "Metaphyseal Dysplasia without Hypotrichosis", "metaphyseal dysplasia without hypotrichosis", "METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS", "cartilage-hair hypoplasia variant, skeletal manifestations only", "Cartilage-Hair Hypoplasia Variant, Skeletal Manifestations Only", "CARTILAGE-HAIR HYPOPLASIA VARIANT, SKELETAL MANIFESTATIONS ONLY", "Cartilage-Hair Hypoplasia-Like Skeletal Dysplasia without Hypotrichosis or Immunodeficiency", "cartilage-hair hypoplasia-like skeletal dysplasia without hypotrichosis or immunodeficiency", "CARTILAGE-HAIR HYPOPLASIA-LIKE SKELETAL DYSPLASIA WITHOUT HYPOTRICHOSIS OR IMMUNODEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metaphyseal dysplasia without hypotrichosis", "shortest_name_length": 4}
{"curie": "MONDO:0019167", "names": ["HSP", "hsp", "Schönlein", "Spring fever", "spring fever", "IgA Vasculitis", "henoch purpura", "Henoch Purpura", "IgA vasculitis", "Vasculitis, IgA", "Purpura, Henoch", "Allergic purpura", "henoch-schonlein", "Henoch's purpura", "Allergic Purpura", "vascular purpura", "PURPURA ALLERGIC", "Purpura allergic", "Henoch-Schonlein", "henoch's purpura", "allergic purpura", "henoch schonlein", "Purpura, Allergic", "allergic; purpura", "PURPURA, ALLERGIC", "purpura; allergic", "Rheumatoid purpura", "Schönlein; purpura", "autoimmune purpura", "Autoimmune purpura", "purpura; Schönlein", "rheumatoid purpura", "Purpura rheumatica", "purpura rheumatica", "purpura, autoimmune", "Purpura, autoimmune", "Anaphylactoid purpura", "Anaphylactoid Purpura", "anaphylactoid purpura", "Purpura anaphylactoid", "PURPURA ANAPHYLACTOID", "Purpura, anaphylactoid", "anaphylactoid; purpura", "Purpura, Anaphylactoid", "purpura; anaphylactoid", "Acute vascular purpura", "Henoch-Scholein purpura", "henoch scholein purpura", "henoch shonlein purpura", "henoch-scholein purpura", "Henoch Shonlein purpura", "HENOCH-SCHONLEIN PURPURA", "Henoch-Schonlein Purpura", "Henoch-Schonlein purpura", "Schonlein-Henoch Purpura", "HENOCH SCHONLEIN PURPURA", "Henoch-Schönlein Purpura", "henoch schonlein purpura", "henoch-schonlein purpura", "Purpura;Henoch-Schonlein", "Henoch Schonlein Purpura", "Henoch-Sch@nlein purpura", "Henoch-Sch?nlein purpura", "Henoch-Schönlein purpura", "Henoch Schonlein purpura", "vascular allergic purpura", "purpura, Schonlein-Henoch", "Schoenlein-Henoch purpura", "Henoch-Schoenlein purpura", "Schonlein Purpura, Henoch", "Henoch Schoenlein Purpura", "allergic vascular purpura", "Purpura vascular allergic", "Schoenlein Henoch Purpura", "Schoenlein-Henoch Purpura", "Purpura, Henoch-Schonlein", "henoch schoenlein purpura", "Henoch-Schonlein Purpuras", "Allergic vascular purpura", "henoch-schoenlein purpura", "Henoch-Schoenlein Purpura", "Schonlein-Henoch Purpuras", "PURPURA VASCULAR ALLERGIC", "HENOCH-SCHOENLEIN PURPURA", "Purpura, Schonlein-Henoch", "Purpura, Schonlein Henoch", "ALLERGIC VASCULAR PURPURA", "Purpura, Henoch Schonlein", "Henoch Schonlein Purpuras", "HENOCH SCHONLEIN SYNDROME", "Schonlein Purpuras, Henoch", "Purpuras, Schonlein-Henoch", "Purpuras, Henoch-Schonlein", "Purpuras, Henoch Schonlein", "Purpura Henoch(-Schönlein)", "Purpura, Henoch-Schoenlein", "Purpura, Schoenlein Henoch", "Purpura, Schoenlein-Henoch", "immunoglobulin A vasculitis", "Immunoglobulin A vasculitis", "allergic purpura (diagnosis)", "Henoch-Schoenlein vasculitis", "Anaphylactic vascular purpura", "ANAPHYLACTIC VASCULAR PURPURA", "Anaphylactoid vascular purpura", "HSP - Henoch-Schonlein purpura", "henoch-schoenlein purpura (HSP)", "Henoch-Schonlein purpura (diagnosis)", "allergic vascular purpura (diagnosis)", "Immunoglobulin A vasculitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunoglobulin A vasculitis", "shortest_name_length": 3}
{"curie": "UMLS:C0862448", "names": ["Renal cancer stage IV", "stage IV kidney cancer", "kidney cancer stage iv", "stage iv kidney cancer", "Kidney cancer stage IV", "kidney cancer, stage IV", "Renal carcinoma stage IV", "metastatic kidney cancer", "Carcinoma kidney stage IV", "Kidney carcinoma stage IV", "Stage IV Renal Cell Cancer", "stage IV renal cell cancer", "renal cell cancer, stage IV", "Renal cell carcinoma stage IV", "stage IV renal cell carcinoma", "renal cell carcinoma, stage IV", "Stage IV Renal Cell Cancer AJCC v6", "Renal Cell Cancer Stage IV AJCC v6", "Stage IV Renal Cell Carcinoma AJCC v6", "Renal Cell Carcinoma, Stage IV AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Renal Cell Cancer", "shortest_name_length": 21}
{"curie": "MONDO:0011132", "names": ["TIDAND", "Nude/SCID", "FOXN1 deficiency", "Winged helix deficiency", "winged helix deficiency", "Pignata Guarino syndrome", "alopecia immunodeficiency", "SCID due to FOXN1 deficiency", "Alymphoid cystic thymic dysgenesis", "alymphoid cystic thymic dysgenesis", "Nude/severe combined immunodeficiency", "Severe combined immunodeficiency due to FOXN1 deficiency", "T-cell immunodeficiency, congenital alopecia and nail dystrophy", "T-CELL IMMUNODEFICIENCY, CONGENITAL ALOPECIA, AND NAIL DYSTROPHY", "T-cell immunodeficiency, congenital alopecia, and nail dystrophy", "T-Cell Immunodeficiency, Congenital Alopecia, And Nail Dystrophy", "Severe T-cell immunodeficiency-congenital alopecia-nail dystrophy syndrome", "severe T-cell immunodeficiency-congenital alopecia-nail dystrophy syndrome", "Severe T-cell immunodeficiency, congenital alopecia, nail dystrophy syndrome", "severe T-cell immunodeficiency, congenital alopecia, nail dystrophy syndrome", "Congenital alopecia and nail dystrophy with severe functional T-cell immunodeficiency", "Severe T-cell immunodeficiency, congenital alopecia, nail dystrophy syndrome (disorder)", "severe T-cell immunodeficiency, congenital alopecia, nail dystrophy syndrome (diagnosis)", "Congenital alopecia and nail dystrophy associated with severe functional T-cell immunodeficiency", "congenital alopecia and nail dystrophy associated with severe functional T-cell immunodeficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-cell immunodeficiency, congenital alopecia, and nail dystrophy", "shortest_name_length": 6}
{"curie": "MONDO:0013894", "names": ["soft", "SOFT", "SOFT syndrome", "SOFT SYNDROME", "soft syndrome", "short stature, onychodysplasia, facial dysmorphism, and hypotrichosis", "SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS", "Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome", "short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome", "Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome", "SOFT (short stature, onychodysplasia, facial dysmorphism, hypotrichosis) syndrome", "Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0012071", "names": ["CGL1", "BSCL1", "Brunzell syndrome AGPAT2-related", "AGPAT2-Related Brunzell Syndrome", "AGPAT2-related Brunzell syndrome", "Syndrome, AGPAT2-Related Brunzell", "Brunzell Syndrome, AGPAT2-Related", "BRUNZELL SYNDROME, AGPAT2-RELATED", "Brunzell Syndrome, AGPAT2 Related", "Brunzell syndrome, AGPAT2-related", "Congenital Generalized Lipodystrophy Type 1", "congenital generalized lipodystrophy type 1", "LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1", "Lipodystrophy, Congenital Generalized, Type 1", "lipodystrophy, congenital generalized, type 1", "Berardinelli Seip Congenital Lipodystrophy Type 1", "Berardinelli-Seip Congenital Lipodystrophy Type 1", "Berardinelli-Seip congenital lipodystrophy type 1", "Berardinelli-Seip congenital lipodystrophy, type 1", "Berardinelli Seip Congenital Lipodystrophy, Type 1", "BERARDINELLI-SEIP CONGENITAL LIPODYSTROPHY, TYPE 1", "Berardinelli-Seip Congenital Lipodystrophy, Type 1", "Lipodystrophy, Berardinelli-Seip Congenital, Type 1", "lipodystrophy, Berardinelli-Seip congenital, type 1", "LIPODYSTROPHY, BERARDINELLI-SEIP CONGENITAL, TYPE 1", "AGPAT2 congenital generalized lipodystrophy (disease)", "congenital generalized lipodystrophy (disease) caused by mutation in AGPAT2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital generalized lipodystrophy type 1", "shortest_name_length": 4}
{"curie": "MONDO:0009451", "names": ["TIDTA", "Nezelof", "athymia", "Athymia", "absent thymus", "Absent thymus", "Thymic Aplasia", "thymic aplasia", "Thymic aplasia", "aplasia; thymic", "thymic; aplasia", "NEZELOF SYNDROME", "Nezelof syndrome", "thymus; agenesis", "agenesis; thymus", "T CELL DEFICIENCY", "t cell deficiency", "Aplasia of thymus", "T-cell deficiency", "Nezelof's syndrome", "Agenesis of thymus", "Absent thymic shadow", "Aplasia of the thymus", "Lack of thymic shadow", "T-LYMPHOCYTE DEFICIENCY", "T-lymphocyte deficiency", "absent thymus (diagnosis)", "Congenital thymus absence", "aplasia congenital thymus", "Congenital thymic aplasia", "Thymic aplasia, congenital", "THYMUS, APLASIA, CONGENITAL", "Aplasia of thymus (disorder)", "Congenital absence of thymus", "Nezelof's syndrome (disorder)", "Agenesis of thymus (disorder)", "Nezelof's syndrome (diagnosis)", "T-lymphocyte deficiency (finding)", "Congenital thymic dysplasia syndrome", "Immune Defect Due To Absence Of Thymus", "immune defect due to absence Of Thymus", "IMMUNE DEFECT DUE TO ABSENCE OF THYMUS", "immune defect due to absence of THYMUS", "Congenital absence of thymus (disorder)", "T-cell immunodeficiency with thymic aplasia", "T-CELL IMMUNODEFICIENCY WITH THYMIC APLASIA", "thymic dysplasia with normal immunoglobulins", "Cellular immunodeficiency with abnormal immunoglobulin deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nezelof syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0017349", "names": ["MPC", "Myopericytoma", "myopericytoma", "Myopericytomas", "Hemangiopericytoma", "hemangiopericytoma", "Solitary Myofibroma", "solitary myofibroma", "Myopericytoma (disorder)", "Myopericytoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopericytoma", "shortest_name_length": 3}
{"curie": "MONDO:0005045", "names": ["HCM", "hocm", "Hypertrophic heart disease", "obstructive cardiomyopathy", "Obstructive cardiomyopathy", "cardiomyopathy hypertrophic", "hypertrophic myocardiopathy", "hypertrophic cardiomyopathy", "CARDIOMYOPATHY HYPERTROPHIC", "Hypertrophic cardiomyopathy", "Cardiomyopathy, obstructive", "Hypertrophic myocardiopathy", "Cardiomyopathy;hypertrophic", "Hypertrophic Cardiomyopathy", "cardiomyopathy; hypertrophic", "hypertrophic; cardiomyopathy", "CARDIOMYOPATHY, HYPERTROPHIC", "Cardiomyopathy, hypertrophic", "Cardiomyopathy, Hypertrophic", "Hypertrophic Cardiomyopathies", "Cardiomyopathies, Hypertrophic", "hypertrophic subaortic stenosis", "HCM - hypertrophic cardiomyopathy", "HCM - Hypertrophic cardiomyopathy", "hypertrophic cardiomyopathy (HCM)", "Enlarged and thickened heart muscle", "familial hypertrophic cardiomyopathy", "Hypertrophic cardiomyopathy (disorder)", "Hypertrophic Obstructive Cardiomyopathy", "Obstructive hypertrophic cardiomyopathy", "obstructive hypertrophic cardiomyopathy", "hypertrophic cardiomyopathy (diagnosis)", "Hypertrophic obstructive cardiomyopathy", "hypertrophic obstructive cardiomyopathy", "Hypertrophic cardiomyopathy, obstructive", "CARDIOMYOPATHY, HYPERTROPHIC OBSTRUCTIVE", "Cardiomyopathy, Hypertrophic Obstructive", "Obstructive Cardiomyopathy, Hypertrophic", "Hypertrophic Obstructive Cardiomyopathies", "cardiomyopathy; hypertrophic, obstructive", "Obstructive Cardiomyopathies, Hypertrophic", "Cardiomyopathies, Hypertrophic Obstructive", "HOCM Hypertrophic obstructive cardiomyopathy", "HOCM - Hypertrophic obstructive cardiomyopathy", "Hypertrophic obstructive cardiomyopathy (disorder)", "obstructive hypertrophic cardiomyopathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophic cardiomyopathy", "shortest_name_length": 3}
{"curie": "UMLS:C5206809", "names": ["Locally Advanced Colorectal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Colorectal Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0000939", "names": ["Intracranial abscess", "Intracranial Abscess", "intracranial abscess", "intracranial; abscess", "abscess; intracranial", "Intracranial abscess, NOS", "Intracranial abscess (disorder)", "intracranial abscess (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intracranial abscess", "shortest_name_length": 20}
{"curie": "MONDO:0004037", "names": ["EDEMA RETINAL", "retinal edema", "RETINAL EDEMA", "Retinal Edema", "Retinal edema", "retina; edema", "edema; retina", "Edema retinal", "Retinal oedema", "RETINAL OEDEMA", "Edema, Retinal", "Oedema retinal", "Retinal Edemas", "Edemas, Retinal", "Retinal edema, NOS", "Retinal oedema, NOS", "Retinal edema (disorder)", "retinal edema (diagnosis)", "retinal edema was observed", "retinal edema (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal edema", "shortest_name_length": 13}
{"curie": "UMLS:C2348656", "names": ["TdT Positive Acute Lymphoblastic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "TdT Positive Acute Lymphoblastic Leukemia", "shortest_name_length": 41}
{"curie": "MONDO:0016829", "names": ["familial visceral myopathy", "Familial visceral myopathy", "visceral myopathy familial", "Visceral Myopathy, Familial", "MEGADUODENUM AND/OR MEGACYSTIS", "Megaduodenum and-or Megacystis", "megaduodenum and/or megacystis", "Megaduodenum and/or megacystis", "Familial hollow visceral myopathy", "Hereditary hollow viscus myopathy", "familial hollow visceral myopathy", "hereditary hollow visceral myopathy", "Hereditary hollow visceral myopathy", "pseudoobstruction idiopathic intestinal", "Hereditary hollow viscus myopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial visceral myopathy", "shortest_name_length": 26}
{"curie": "MONDO:0003989", "names": ["polyembryoma", "Ovarian Polyembryoma", "ovarian polyembryoma", "polyembryoma, ovarian", "polyembryoma of ovary", "polyembryoma of the ovary", "Polyembryoma of the Ovary", "polyembryoma of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyembryoma of the ovary", "shortest_name_length": 12}
{"curie": "UMLS:C0856009", "names": ["Stage II Supradiaphragmatic Nodular Sclerosis Hodgkin Lymphoma", "Hodgkin's disease nodular sclerosis stage II supradiaphragmatic", "Stage II Supradiaphragmatic Nodular Sclerosis Hodgkin's Disease", "Stage II Nodular Sclerosis Hodgkin's Disease above the Diaphragm", "Stage II Supradiaphragmatic Nodular Sclerosis Hodgkin's Lymphoma", "Stage II Nodular Sclerosis Hodgkin's Lymphoma above the Diaphragm", "Stage II Supradiaphragmatic Nodular Sclerosis Classical Hodgkin Lymphoma", "Ann Arbor Stage II Supradiaphragmatic Nodular Sclerosis Classic Hodgkin Lymphoma", "Ann Arbor Stage II Supradiaphragmatic Nodular Sclerosis Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's disease nodular sclerosis stage II supradiaphragmatic", "shortest_name_length": 62}
{"curie": "MONDO:0001351", "names": ["uterine adnexa cancer", "malignant neoplasm of uterine adnexa", "Malignant neoplasm of uterine adnexa", "Malignant neoplasm of uterine adnexa, NOS", "Malignant neoplasm of uterine adnexa (disorder)", "malignant neoplasm of uterine adnexa (diagnosis)", "Malignant neoplasm of uterine adnexa, unspecified", "Malignant neoplasm of ovary and other uterine adnexa", "Malignant neoplasm of uterine adnexa, unspecified site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine adnexa cancer", "shortest_name_length": 21}
{"curie": "UMLS:C4688420", "names": ["IVB", "stage IVB prostate cancer", "Stage IVB Prostate Cancer", "stage IVB prostate cancer AJCC v8", "Stage IVB Prostate Cancer AJCC v8", "Stage IVB Prostate Carcinoma AJCC v8", "stage IVB prostate carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Prostate Cancer AJCC v8", "shortest_name_length": 3}
{"curie": "MONDO:0017710", "names": ["congenital systemic veins anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital systemic veins anomaly", "shortest_name_length": 33}
{"curie": "MONDO:0015567", "names": ["cataract - glaucoma", "Cataract glaucoma syndrome", "cataract-glaucoma syndrome", "Cataract-glaucoma syndrome", "Cataract glaucoma syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract-glaucoma syndrome", "shortest_name_length": 19}
{"curie": "UMLS:C4054911", "names": ["Fusion-Positive Rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fusion-Positive Rhabdomyosarcoma", "shortest_name_length": 32}
{"curie": "UMLS:C1142239", "names": ["call-fleming syndrome", "call fleming syndrome", "Call-Fleming syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Call-Fleming syndrome", "shortest_name_length": 21}
{"curie": "UMLS:C1333490", "names": ["External Ear Actinic Keratosis", "Actinic Keratosis of External Ear", "Actinic Keratosis of the External Ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "External Ear Actinic Keratosis", "shortest_name_length": 30}
{"curie": "UMLS:C0854911", "names": ["CNS Epidermoid Cyst", "CNS Epidermoid Tumor", "Epidermoid Cyst of CNS", "Epidermoid Tumor of CNS", "CNS Epidermoid Neoplasm", "Epidermoid Cyst of the CNS", "Epidermoid Neoplasm of CNS", "Epidermoid Tumor of the CNS", "Epidermoid Neoplasm of the CNS", "Central Nervous System Epidermoid Cyst", "Central nervous system epidermoid tumor", "Central Nervous System Epidermoid Tumor", "Central nervous system epidermoid tumour", "Epidermoid Cyst of Central Nervous System", "Central Nervous System Epidermoid Neoplasm", "Epidermoid Tumor of Central Nervous System", "Epidermoid Cyst of the Central Nervous System", "Epidermoid Neoplasm of Central Nervous System", "Epidermoid Tumor of the Central Nervous System", "Epidermoid Neoplasm of the Central Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central nervous system epidermoid tumor", "shortest_name_length": 19}
{"curie": "MONDO:0003335", "names": ["chronic polyneuropathy", "Polyneuropathy chronic", "Chronic Polyneuropathy", "polyneuropathy, chronic", "Chronic polyneuropathies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic polyneuropathy", "shortest_name_length": 22}
{"curie": "UMLS:C5420303", "names": ["Unresectable Peritoneal Malignant Mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Peritoneal Malignant Mesothelioma", "shortest_name_length": 46}
{"curie": "MONDO:0030827", "names": ["MACTHC2", "macrothrombocytopenia, isolated, 2, autosomal dominant", "MACROTHROMBOCYTOPENIA, ISOLATED, 2, AUTOSOMAL DOMINANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macrothrombocytopenia, isolated, 2, autosomal dominant", "shortest_name_length": 7}
{"curie": "MONDO:0010439", "names": ["CARDIOMYOPATHY, FATAL FETAL, DUE TO MYOCARDIAL CALCIFICATION", "Cardiomyopathy, fatal fetal, due to myocardial calcification", "cardiomyopathy, fatal fetal, due to myocardial calcification", "Myocardial calcifications resulting in intrauterine fetal death", "myocardial calcifications resulting in intrauterine fetal death"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiomyopathy, fatal fetal, due to myocardial calcification", "shortest_name_length": 60}
{"curie": "UMLS:C4525139", "names": ["stage IIIB rectal cancer", "Stage IIIB Rectal Cancer", "Stage IIIB Rectal Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Rectal Cancer AJCC v8", "shortest_name_length": 24}
{"curie": "MONDO:0004686", "names": ["Finland type amyloidosis", "Finnish type amyloidosis", "Amyloid corneal dystrophy", "Lattice corneal dystrophy", "lattice corneal dystrophy", "Biber haab dimmer dystrophy", "Lattice dystrophy of cornea", "Amyloid Neuropathies, Familial", "lattice corneal dystrophy (disease)", "Lattice corneal dystrophy (disorder)", "lattice corneal dystrophy (diagnosis)", "Familial amyloid polyneuropathy type V", "Type V Familial Amyloid Polyneuropathy", "Familial Amyloid Polyneuropathy, Type V", "Finnish Type Familial Amyloid Neuropathy", "familial amyloid neuropathy, Finnish type", "Familial amyloid neuropathy, Finnish type", "Familial Amyloid Neuropathy, Finnish Type", "Amyloid cranial neuropathy with lattice corneal dystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lattice corneal dystrophy", "shortest_name_length": 24}
{"curie": "MONDO:0012883", "names": ["M3", "APL", "APML", "FAB M3", "AML M3", "fab m3", "M3 ANLL", "ANLL, M3", "promyelocytic leukemia", "Promyelocytic Leukemia", "promyelocytic; leukemia", "LEUKEMIA, PROMYELOCYTIC", "leukemia; promyelocytic", "Progranulocytic Leukemia", "progranulocytic leukemia", "Leukemia, Progranulocytic", "acute myeloid leukemia M3", "AML with t(15;17)(q22;q12)", "acute myeloid leukaemia M3", "Myeloid Leukemia, Acute, M3", "Leukemia, Myeloid, Acute, M3", "leukemia acute promyelocytic", "Acute Promyelocytic Leukemia", "LEUKEMIA ACUTE PROMYELOCYTIC", "ACUTE PROMYELOCYTIC LEUKEMIA", "acute promyelocytic leukemia", "Acute promyelocytic leukemia", "LEUKEMIA, ACUTE PROMYELOCYTIC", "Acute Promyelocytic Leukemias", "leukemia, acute promyelocytic", "Promyelocytic Leukemia, Acute", "Leukemia, Acute Promyelocytic", "acute myeloblastic leukemia 3", "Acute myeloblastic leukemia 3", "acute promyelocytic leukaemia", "Acute promyelocytic leukaemia", "Leukemia, Promyelocytic, Acute", "[M]Acute promyelocytic leukemia", "M3 acute promyelocytic leukemia", "[M]Acute promyelocytic leukaemia", "acute promyelocytic leukemia apl", "Acute promyelocytic leukemia NOS", "M3 - Acute promyelocytic leukemia", "M3 - Acute promyelocytic leukaemia", "acute myeloblastic leukemia type 3", "APL - Acute promyelocytic leukemia", "APML - Acute promyelocytic leukemia", "acute myeloblastic leukaemia type 3", "APML - acute promyelocytic leukemia", "APL - Acute promyelocytic leukaemia", "APML - Acute promyelocytic leukaemia", "Acute promyelocytic leukemia, FAB M3", "Acute promyelocytic leukaemia, FAB M3", "Acute myeloid leukemia, PML/RAR-alpha", "leukemia, acute promyelocytic, somatic", "Acute myeloid leukaemia, PML/RAR-alpha", "Acute promyelocytic leukemia (clinical)", "Acute promyelocytic leukaemia (clinical)", "acute promyelocytic leukemia (diagnosis)", "acute promyelocytic leukemia with PML-RARA", "Acute Promyelocytic Leukemia with PML-RARA", "acute promyelocytic leukemia with PML-rara", "Acute promyelocytic leukemia, PML/RAR-alpha", "Acute promyelocytic leukaemia, PML/RAR-alpha", "Acute promyelocytic leukaemia, PML-RAR-alpha", "Acute myeloid leukemia, t(15;17)(q22;q11-12)", "Acute myeloid leukaemia, t(15;17)(q22;q11-12)", "Acute promyelocytic leukemia, FAB M3 (disorder)", "acute promyelocytic leukemia, t(15;17)(q22;q11-12)", "Acute promyelocytic leukemia, t(15;17)(q22;q11-12)", "Acute promyelocytic leukaemia, t(15;17)(q22;q11-12)", "AML with t(15;17)(q22;q12);(PML/RARalpha) and variants", "acute promyelocytic leukemia with t(15;17)(q22;q12); PML-rara", "Acute Promyelocytic Leukemia with t(15;17)(q22;q12); PML-RARA", "acute promyelocytic leukemia with t(15;17)(q22;q12); PML/rara", "Acute Promyelocytic Leukemia with t(15;17)(q22;q12); PML/RARA", "M3 OR Acute Promyelocytic Leukemia with t(15;17)(q22;q12); PML-RARA", "Acute myeloid leukemia with t(15;17)(q22;q12);(PML/RARalpha) and variants", "acute myeloid leukemia with t(15;17)(q22;q12);(PML/RARalpha) and variants", "Acute promyelocytic leukemia, t(15;17)(q22;q11-12) (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute promyelocytic leukemia", "shortest_name_length": 2}
{"curie": "MONDO:0000457", "names": ["Classical Glioblastoma", "classical glioblastoma", "glioblastoma classical subtype"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "classical glioblastoma", "shortest_name_length": 22}
{"curie": "UMLS:C5555046", "names": ["Mucosal Melanoma of the Urinary Tract", "Mucosal Melanoma of the Urinary System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mucosal Melanoma of the Urinary System", "shortest_name_length": 37}
{"curie": "UMLS:C1336055", "names": ["Uveal Spindle Cell Type B Melanoma", "Spindle Cell Type B Uveal Melanoma", "Spindle Cell Type B Melanoma of Uvea", "Spindle Cell Type B Melanoma of the Uvea", "B type spindle cell intraocular melanoma", "spindle cell B type intraocular melanoma", "type B spindle cell intraocular melanoma", "intraocular melanoma, spindle cell B type", "melanoma, spindle cell B type intraocular", "melanoma, intraocular, spindle cell B type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uveal Spindle Cell Type B Melanoma", "shortest_name_length": 34}
{"curie": "UMLS:C5447847", "names": ["Epithelioid Hemangioendothelioma with YAP1-TFE3 Gene Fusion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epithelioid Hemangioendothelioma with YAP1-TFE3 Gene Fusion", "shortest_name_length": 59}
{"curie": "MONDO:0010117", "names": ["3M1", "3M syndrome", "3M syndrome 1", "3-M syndrome 1", "CUL7 3-M syndrome", "Cul7 3-M syndrome", "Three M Syndrome 1", "Le Merrer Syndrome", "Le Merrer syndrome", "THREE M SYNDROME 1", "LE MERRER SYNDROME", "three M syndrome 1", "Gloomy Face Syndrome", "GLOOMY FACE SYNDROME", "gloomy face syndrome", "three M syndrome type 1", "Dolichospondylic dysplasia", "Dolichospondylic Dysplasia", "DOLICHOSPONDYLIC DYSPLASIA", "YAKUT SHORT STATURE SYNDROME", "Yakut short stature syndrome", "Three-M Slender-Boned Nanism", "Yakut Short Stature Syndrome", "3-M syndrome caused by mutation in Cul7", "3-M syndrome caused by mutation in CUL7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "3M syndrome 1", "shortest_name_length": 3}
{"curie": "UMLS:C1262241", "names": ["Gastric melanoma", "Gastric Melanoma", "Gastric Mucosal Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric melanoma", "shortest_name_length": 16}
{"curie": "UMLS:C1167720", "names": ["stage I pancreas cancer", "pancreas cancer, stage I", "stage I pancreatic cancer", "pancreatic cancer, stage I", "Pancreatic carcinoma stage I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic carcinoma stage I", "shortest_name_length": 23}
{"curie": "UMLS:C4744720", "names": ["High Risk Acute Myeloid Leukemia", "High-Risk Acute Myeloid Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Risk Acute Myeloid Leukemia", "shortest_name_length": 32}
{"curie": "MONDO:0000208", "names": ["MSSGM", "MSSGM1", "MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM", "microcephaly, short stature, and impaired glucose metabolism", "MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 1", "microcephaly, short stature, and impaired glucose metabolism 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly, short stature, and impaired glucose metabolism 1", "shortest_name_length": 5}
{"curie": "UMLS:C1336957", "names": ["Very Low Risk Colorectal Gastrointestinal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Very Low Risk Colorectal Gastrointestinal Stromal Tumor", "shortest_name_length": 55}
{"curie": "MONDO:0011740", "names": ["Carney dyad", "Carney-Stratakis dyad", "Carney Stratakis dyad", "paraganglioma and gist", "gist-paraganglioma dyad", "GIST-paraganglioma dyad", "Carney Stratakis syndrome", "Carney-Stratakis syndrome", "CARNEY-STRATAKIS SYNDROME", "Carney-Stratakis Syndrome", "paraganglioma and gastric stromal sarcoma", "Paraganglioma and Gastric Stromal Sarcoma", "PARAGANGLIOMA AND GASTRIC STROMAL SARCOMA", "Paraganglioma and gastric stromal sarcoma", "paraganglioma and gastrointestinal stromal tumor", "Paraganglioma and Gastrointestinal Stromal Tumor", "PARAGANGLIOMA AND GASTROINTESTINAL STROMAL TUMOR", "Paraganglioma and gastric stromal sarcoma syndrome", "Paraganglioma and gastric stromal sarcoma syndrome (disorder)", "Carney-Stratakis dyad of paraganglioma and gastric stromal sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carney-Stratakis syndrome", "shortest_name_length": 11}
{"curie": "UMLS:C0554628", "names": ["Group A Strep Infection", "group A Streptococcal infection", "Group A Streptococcal Infection", "Streptococcus pyogenes infection", "Group A Streptococcal Infections", "Infection due to Streptococcus group A", "group A Streptococcal infection (diagnosis)", "Streptococcus pyogenes infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Group A Streptococcal Infections", "shortest_name_length": 23}
{"curie": "UMLS:C4744551", "names": ["Metastatic Nasopharyngeal Undifferentiated Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Nasopharyngeal Undifferentiated Carcinoma", "shortest_name_length": 52}
{"curie": "MONDO:0019641", "names": ["Pauci-immune glomerulonephritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pauci-immune glomerulonephritis", "shortest_name_length": 31}
{"curie": "MONDO:0009785", "names": ["OPSMD", "opsismodysplasia", "OPSISMODYSPLASIA", "Opsismodysplasia", "Opsismodysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "opsismodysplasia", "shortest_name_length": 5}
{"curie": "UMLS:C1336276", "names": ["Ureter Cancer Stage III", "Stage III Ureter Cancer", "Stage III Ureter Carcinoma", "Stage III Ureteral Carcinoma", "Stage III Carcinoma of Ureter", "Stage III Ureter Cancer AJCC v7", "Stage III Carcinoma of the Ureter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Ureter Cancer AJCC v7", "shortest_name_length": 23}
{"curie": "MONDO:0017704", "names": ["familial partial epilepsy", "hereditary partial epilepsy", "epilepsy, partial, familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial partial epilepsy", "shortest_name_length": 25}
{"curie": "MONDO:0015784", "names": ["Prader-Willi Syndrome (Type 2)", "Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2", "shortest_name_length": 30}
{"curie": "MONDO:0002535", "names": ["Verrucous Papilloma", "Verrucous papilloma", "verrucous papilloma", "Verrucous papilloma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "verrucous papilloma", "shortest_name_length": 19}
{"curie": "UMLS:C1709569", "names": ["PHAT", "Early Pleomorphic Hyalinizing Angiectatic Tumor", "Pleomorphic hyalinizing angiectatic tumor of soft parts", "Pleomorphic Hyalinizing Angiectatic Tumor of Soft Parts", "Pleomorphic hyalinizing angiectatic tumor of soft tissue", "Pleomorphic hyalinising angiectatic tumour of soft parts", "Pleomorphic hyalinising angiectatic tumour of soft tissue", "Pleomorphic hyalinising angiectatic neoplasm of soft parts", "Pleomorphic hyalinizing angiectatic neoplasm of soft parts", "Pleomorphic hyalinising angiectatic neoplasm of soft tissue", "Pleomorphic hyalinizing angiectatic neoplasm of soft tissue", "Pleomorphic hyalinizing angiectatic tumor of soft tissue (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pleomorphic hyalinizing angiectatic tumor of soft tissue", "shortest_name_length": 4}
{"curie": "MONDO:0006551", "names": ["Alopecia Mucinosa", "alopecia Mucinosa", "alopecia mucinosa", "Alopecia mucinosa", "mucinosa; alopecia", "alopecia; mucinosa", "alopecia mucinosis", "Alopecia Mucinosis", "Follicular Mucinoses", "Follicular mucinosis", "follicular mucinosis", "Follicular Mucinosis", "Mucinoses, Follicular", "Mucinosis, Follicular", "Alopecia mucinosa (disorder)", "alopecia mucinosa (diagnosis)", "hair follicle cutaneous focal mucinosis", "cutaneous focal mucinosis of hair follicle"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alopecia mucinosa", "shortest_name_length": 17}
{"curie": "UMLS:C3804961", "names": ["Diabetic metabolic decompensation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diabetic metabolic decompensation", "shortest_name_length": 33}
{"curie": "MONDO:0011415", "names": ["LCA3", "RP94", "LEBER CONGENITAL AMAUROSIS 3", "Leber congenital amaurosis 3", "Leber Congenital Amaurosis 3", "SPATA7 Leber congenital amaurosis", "Leber congenital amaurosis type 3", "amaurosis congenita of Leber, type 3", "LEBER CONGENITAL AMAUROSIS 3 (disorder)", "RETINITIS PIGMENTOSA 94, VARIABLE AGE AT ONSET", "retinitis pigmentosa, juvenile, Spata7-related", "retinitis pigmentosa, juvenile, autosomal recessive", "Leber congenital amaurosis caused by mutation in SPATA7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leber congenital amaurosis 3", "shortest_name_length": 4}
{"curie": "UMLS:C0278691", "names": ["localized resectable neuroblastoma", "Localized Resectable Neuroblastoma", "neuroblastoma, localized resectable"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized Resectable Neuroblastoma", "shortest_name_length": 34}
{"curie": "UMLS:C5420305", "names": ["Unresectable Peritoneal Sarcomatoid Mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Peritoneal Sarcomatoid Mesothelioma", "shortest_name_length": 48}
{"curie": "UMLS:C1333142", "names": ["Congenital Adrenal Gland Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Adrenal Gland Disorder", "shortest_name_length": 33}
{"curie": "UMLS:C1963921", "names": ["Chemical phlebitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chemical phlebitis", "shortest_name_length": 18}
{"curie": "UMLS:C1336360", "names": ["Stage IVA Vulvar Cancer", "Stage IVA Vulva Cancer AJCC v6", "Stage IVA Vulvar Cancer AJCC v6", "Stage IVA Vulval Cancer AJCC v6", "Stage IVA Vulva Carcinoma AJCC v6", "Stage IVA Vulval Carcinoma AJCC v6", "Stage IVA Vulvar Carcinoma AJCC v6", "Stage IVA Carcinoma of Vulva AJCC v6", "Stage IVA Carcinoma of the Vulva AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Vulvar Cancer AJCC v6", "shortest_name_length": 23}
{"curie": "MONDO:0011269", "names": ["PSORS2", "psoriasis 2", "PSORIASIS 2", "CARD14 psoriasis", "psoriasis type 2", "psoriasis caused by mutation in CARD14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "psoriasis 2", "shortest_name_length": 6}
{"curie": "UMLS:C2212884", "names": ["Lacrimal Gland Lymphoma", "Primary Lacrimal Gland Lymphoma", "Lacrimal Gland Non-Hodgkin Lymphoma", "non-Hodgkin's lymphoma of lacrimal gland", "Primary Lacrimal Gland Non-Hodgkin Lymphoma", "non-Hodgkin's lymphoma of lacrimal gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-Hodgkin's lymphoma of lacrimal gland", "shortest_name_length": 23}
{"curie": "MONDO:0004854", "names": ["Ophthalmia neonatorum", "OPHTHALMIA NEONATORUM", "ophthalmia neonatorum", "neonatorum ophthalmia", "Ophthalmia Neonatorum", "neonatorum; ophthalmia", "ophthalmia; neonatorum", "Neonatal conjunctivitis", "neonatal conjunctivitis", "CONJUNCTIVITIS NEONATAL", "conjunctivitis neonatal", "Neonatal Conjunctivitis", "neonatal; conjunctivitis", "conjunctivitis; neonatal", "Conjunctivitis, Infantile", "Ophthalmia neonatorum NOS", "Gonococcal conjunctivitis", "Ophthalmia neonatorum, NOS", "Neonatal conjunctivitis NOS", "Neonatal conjunctivitis, NOS", "gonococcal ophthalmia neonatorum", "Gonococcal ophthalmia neonatorum", "Neonatal conjunctivitis (disorder)", "neonatal conjunctivitis (diagnosis)", "gonococcal conjunctivitis (neonatorum)", "Neonatal dacryocystitis and conjunctivitis", "Neonatal conjunctivitis and dacryocystitis", "Neonatal dacryocystitis and conjunctivitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ophthalmia neonatorum", "shortest_name_length": 21}
{"curie": "UMLS:C4682893", "names": ["Renal Pelvis and Ureter Cancer by AJCC v7 Stage", "Renal Pelvis and Ureter Urothelial Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal Pelvis and Ureter Cancer by AJCC v7 Stage", "shortest_name_length": 47}
{"curie": "MONDO:0014205", "names": ["BRPS", "ASXL3-related disorder", "ASXL3 deficiency syndrome", "BAINBRIDGE-ROPERS SYNDROME", "Bainbridge-Ropers syndrome", "BAINBRIDGE-ROPERS syndrome", "Bainbridge-Roppers syndrome", "Bainbridge Roppers syndrome", "severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome", "Severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome", "Severe feeding difficulties, failure to thrive, microcephaly due to ASXL3 deficiency syndrome", "Severe feeding difficulties, failure to thrive, microcephaly due to ASXL3 deficiency syndrome (diagnosis)", "Severe feeding difficulties, failure to thrive, microcephaly due to ASXL transcriptional regulator 3 deficiency syndrome", "Severe feeding difficulties, failure to thrive, microcephaly due to ASXL transcriptional regulator 3 deficiency syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0151846", "names": ["periosteum", "Periosteal Disorder", "Disorder periosteal", "PERIOSTEAL DISORDER", "Periosteal disorder", "DISORDER PERIOSTEAL", "periosteum; disorder", "disease (or disorder); periosteum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Periosteal Disorder", "shortest_name_length": 10}
{"curie": "UMLS:C0876993", "names": ["ventricular thrombus", "VENTRICULAR THROMBUS", "ventricle; thrombosis", "Ventricular thrombosis", "ventricular thrombosis", "thrombosis; ventricular", "Cardiac ventricular thrombosis", "ventricular thrombosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiac ventricular thrombosis", "shortest_name_length": 20}
{"curie": "MONDO:0007804", "names": ["PHS", "CAVE Complex", "Complex, CAVE", "CAVE Complices", "Hall syndrome 2", "Complices, CAVE", "pallister hall syndrome", "Pallister Hall Syndrome", "Pallister-Hall Syndrome", "Pallister Hall syndrome", "pallister-hall syndrome", "PALLISTER-HALL SYNDROME", "Hall Pallister Syndrome", "Pallister-Hall syndrome", "Hall-Pallister Syndrome", "Syndrome, Pallister-Hall", "Syndrome, Hall-Pallister", "hamartopolydactyly syndrome", "ano-cerebro-digital syndrome", "Ano-cerebro-digital Syndrome", "Pallister-Hall syndrome (disorder)", "Hypothalamic hamartoblastoma syndrome", "hypothalamic hamartoblastoma syndrome", "Hypothalamic Hamartoblastoma Syndrome", "Hypothalamic Hamartoblastoma Syndromes", "Hamartoblastoma Syndrome, Hypothalamic", "Syndrome, Hypothalamic Hamartoblastoma", "Syndromes, Hypothalamic Hamartoblastoma", "Hamartoblastoma Syndromes, Hypothalamic", "congenital hypothalamic hamartoblastoma", "Cerebroacrovisceral Early Lethality Complex", "renal-anal-lung-polydactyly-hamartoblastoma syndrome", "renal-anal-lung-polydactyly-hamartoblastoma (RALPH) syndrome", "hypothalamic hamartoblastoma-hyperphalangeal hypoendocrine-hypoplastic anus (4H) syndrome", "HYPOTHALAMIC HAMARTOBLASTOMA, HYPOPITUITARISM, IMPERFORATE ANUS, AND POSTAXIAL POLYDACTYLY", "hypothalamic hamartoblastoma, hypopituitarism, imperforate anus, and postaxial polydactyly", "Hypothalamic Hamartoblastoma, Hypopituitarism, Imperforate Anus, and Postaxial Polydactyly", "hypothalamic hamartoblastoma-hypopituitarism-imperforate anus-postaxial polydactyly syndrome", "microphallus-imperforate anus-syndactyly-hamartoblastoma-abnormal lung lobulation-polydactyly syndrome", "microphallus-imperforate anus-syndactyly-hamartoblastoma-abnormal lung lobulation-polydactyly (MISHAP) syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pallister-Hall syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C1335021", "names": ["Non-Neoplastic Nasal Cavity Disease", "Non-Neoplastic Nasal Cavity Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Nasal Cavity Disorder", "shortest_name_length": 35}
{"curie": "UMLS:C0274968", "names": ["organophosphate poison", "organophosphate toxicity", "Phosphate salt poisoning", "Organophosphate toxicity", "organophosphate poisoning", "Organophosphate Poisoning", "ORGANOPHOSPHATE POISONING", "Organophosphate poisoning", "organophosphates poisoning", "Poisoning, Organophosphate", "Organophosphate Poisonings", "Organic phosphate poisoning", "Poisonings, Organophosphate", "organic phosphate poisoning", "phosphate organic poisoning", "ORGANIC PHOSPHATE POISONING", "poisoning by organophosphate", "Organophosphate intoxication", "Phosphate salt poisoning (disorder)", "Organophosphate poisoning (disorder)", "Organophosphate insecticide poisoning", "Poisoning of animals with phosphate salts", "poisoning by organophosphate insecticides", "poisoning by organophosphorus insecticides", "Organophosphate insecticide causing toxic effect", "poisoning by organophosphate insecticides (diagnosis)", "poisoning by organophosphorus insecticides (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Poisoning of animals with phosphate salts", "shortest_name_length": 22}
{"curie": "UMLS:C0854817", "names": ["Stage IV Lymphoplasmacytic Lymphoma", "Ann Arbor Stage IV Lymphoplasmacytic Lymphoma", "Lymphoplasmacytoid lymphoma/immunocytoma stage IV", "Stage IV Lymphoplasmacytoid Lymphoma/Immunocytoma", "Lymphoplasmacytoid Lymphoma/Immunocytoma Stage IV"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoplasmacytoid lymphoma/immunocytoma stage IV", "shortest_name_length": 35}
{"curie": "MONDO:0010802", "names": ["HDCA", "PACHD", "Yorifuji-Okuno syndrome", "Yorifuji Okuno syndrome", "Pancreatic hypoplasia diabetes heart disease", "PANCREATIC AGENESIS AND CONGENITAL HEART DEFECTS", "pancreatic agenesis and congenital heart defects", "congenital heart defects and other congenital anomalies", "HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES", "heart defects, congenital, and other congenital anomalies", "Pancreatic hypoplasia-diabetes-congenital heart disease syndrome", "pancreatic hypoplasia-diabetes-congenital heart disease syndrome", "Pancreatic hypoplasia, diabetes mellitus, congenital heart disease syndrome", "hereditary pancreatic hypoplasia, diabetes mellitus and congenital heart disease", "congenital pancreatic hypoplasia with diabetes mellitus and congenital heart disease", "pancreatic hypoplasia, congenital, with diabetes mellitus and congenital heart disease", "PANCREATIC HYPOPLASIA, CONGENITAL, WITH DIABETES MELLITUS AND CONGENITAL HEART DISEASE", "Pancreatic Hypoplasia, Congenital, with Diabetes Mellitus and Congenital Heart Disease", "Pancreatic hypoplasia, diabetes mellitus, congenital heart disease syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic hypoplasia-diabetes-congenital heart disease syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C1704615", "names": ["Cardiac Malignant Fibrous Histiocytoma", "Cardiac Unclassified Pleomorphic Sarcoma", "Heart Undifferentiated Pleomorphic Sarcoma", "Cardiac Undifferentiated Pleomorphic Sarcoma", "Cardiac Unclassified Pleomorphic Sarcoma (Formerly Cardiac \"MFH\")", "Cardiac Unclassified Pleomorphic Sarcoma (Formerly Cardiac \"Malignant Fibrous Histiocytoma\")"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiac Malignant Fibrous Histiocytoma", "shortest_name_length": 38}
{"curie": "MONDO:0006422", "names": ["Small Intestinal Tubulovillous Adenoma", "small intestinal tubulovillous adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small intestinal tubulovillous adenoma", "shortest_name_length": 38}
{"curie": "UMLS:C3273239", "names": ["PIA", "Proliferative Inflammatory Atrophy", "Prostate Proliferative Inflammatory Atrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Proliferative Inflammatory Atrophy", "shortest_name_length": 3}
{"curie": "MONDO:0011688", "names": ["MDC1C", "MDDGB5", "congenital muscular dystrophy 1C", "Muscular Dystrophy, Congenital, 1C", "muscular dystrophy, congenital, 1C", "MUSCULAR DYSTROPHY, CONGENITAL, 1C", "FKRP-related congenital muscular dystrophy", "congenital muscular dystrophy-FKRP related", "muscular dystrophy, congenital, FKRP-related", "MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED", "muscular dystrophy-dystroglycanopathy type B5", "muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type B, 5", "muscular dystrophy-dystroglycanopathy (congenital with or without intellectual disability), type B, 5", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT), TYPE B, 5", "muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy-dystroglycanopathy type B5", "shortest_name_length": 5}
{"curie": "MONDO:0015738", "names": ["mild nemaline myopathy", "childhood-onset nemaline myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood-onset nemaline myopathy", "shortest_name_length": 22}
{"curie": "UMLS:C5206674", "names": ["Penile Lymphangioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Penile Lymphangioma", "shortest_name_length": 19}
{"curie": "UMLS:C5670976", "names": ["Methotrexate-Related Burkitt Lymphoma", "Methotrexate-Related Burkitt's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Methotrexate-Related Burkitt Lymphoma", "shortest_name_length": 37}
{"curie": "UMLS:C0334278", "names": ["superficial spreading adenocarcinoma", "Superficial Spreading Adenocarcinoma", "Superficial spreading adenocarcinoma", "superficial spreading adenocarcinoma (diagnosis)", "malignant neoplasm adenocarcinoma superficial spreading", "Superficial spreading adenocarcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Superficial spreading adenocarcinoma", "shortest_name_length": 36}
{"curie": "MONDO:0001856", "names": ["splenic artery aneurysm", "Splenic artery aneurysm", "aneurysm artery splenic", "aneurysm; splenic artery", "aneurysms artery splenic", "Aneurysm of splenic artery", "splenic artery aneurysm (diagnosis)", "Aneurysm of splenic artery (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "splenic artery aneurysm", "shortest_name_length": 23}
{"curie": "MONDO:0016417", "names": ["congenital ichthyosis-microcephalus-tetraplegia syndrome", "congenital ichthyosis-microcephalus-quadriplegia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital ichthyosis-microcephalus-tetraplegia syndrome", "shortest_name_length": 56}
{"curie": "UMLS:C2981610", "names": ["Stage I Digestive System Neuroendocrine Tumor", "Stage I Gastrointestinal Neuroendocrine Neoplasm", "Stage I Digestive System Neuroendocrine Neoplasm", "Stage I Digestive System Neuroendocrine Tumor AJCC v7", "Stage I Gastrointestinal Neuroendocrine Neoplasm AJCC v7", "Stage I Digestive System Neuroendocrine Neoplasm AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Digestive System Neuroendocrine Tumor AJCC v7", "shortest_name_length": 45}
{"curie": "UMLS:C4727077", "names": ["Locally Advanced Skin Squamous Cell Carcinoma", "Locally Advanced Cutaneous Squamous Cell Carcinoma", "locally advanced squamous cell carcinoma of the skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Skin Squamous Cell Carcinoma", "shortest_name_length": 45}
{"curie": "MONDO:0020731", "names": ["ARBOVIRUS INFECT", "Arboviral disease", "Arbovirus infection", "Arbovirus Infection", "arbovirus infection", "Arbovirus Infections", "Infection, Arbovirus", "Arbovirus infections", "Infections, Arbovirus", "Arbovirus infection NOS", "Arbovirus infection, NOS", "Arthropod-borne viral disease", "ARTHROPOD-BORNE VIRAL DISEASES", "Arbovirus infection (disorder)", "viral; disease, arthropod-borne", "arthropod-borne viral infection", "Arthropod-Borne Viral Infection", "Arthropod-borne viral infection", "arthropod-borne; disease (virus)", "Arthropod-borne viral disease, unspecified", "infection; viral, arboviral (arthropod-borne)", "disease (or disorder); viral, arthropod-borne", "viral; infection, arboviral (arthropod-borne)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arbovirus infection", "shortest_name_length": 16}
{"curie": "UMLS:C5204274", "names": ["Renal Germ Cell Tumor", "Kidney Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kidney Germ Cell Tumor", "shortest_name_length": 21}
{"curie": "MONDO:0008423", "names": ["SSS-MYOPIA SYNDROME", "SSS-Myopia Syndrome", "Sss-myopia syndrome", "Sinus Node Disease and Myopia", "SINUS NODE DISEASE AND MYOPIA", "sinus node disease and myopia", "Sick Sinus Syndrome and Myopia", "SICK SINUS SYNDROME AND MYOPIA", "sick sinus syndrome and myopia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sinus node disease and myopia", "shortest_name_length": 19}
{"curie": "UMLS:C0271389", "names": ["Jerk Nystagmus", "Jerk nystagmus", "nystagmus jerk", "Nystagmus, Jerk", "Nystagmus, jerk", "Rhythmical nystagmus", "Acquired jerk nystagmus", "Jerk nystagmus (disorder)", "Jerk nystagmus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jerk Nystagmus", "shortest_name_length": 14}
{"curie": "MONDO:0008169", "names": ["OSTEOCHONDRODYSPLASIA, RHIZOMELIC, WITH CALLOSAL AGENESIS, THROMBOCYTOPENIA, HYDROCEPHALUS, AND HYPERTENSION", "Osteochondrodysplasia, Rhizomelic, with Callosal Agenesis, Thrombocytopenia, Hydrocephalus, and Hypertension", "osteochondrodysplasia, rhizomelic, with callosal agenesis, thrombocytopenia, hydrocephalus, and hypertension", "osteochondrodysplasia with rhizomelia, platyspondyly, callosal agenesis, thrombocytopenia, hydrocephalus, and hypertension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteochondrodysplasia, rhizomelic, with callosal agenesis, thrombocytopenia, hydrocephalus, and hypertension", "shortest_name_length": 108}
{"curie": "MONDO:0021235", "names": ["External Ear Tumor", "external ear tumor", "external Ear tumor", "ear external tumors", "External Ear Neoplasm", "external ear neoplasm", "tumor of external Ear", "Tumor of external ear", "tumor of external ear", "Tumor of External Ear", "Tumour of external ear", "Neoplasm of External Ear", "neoplasm of external Ear", "neoplasm of external ear", "Tumor of the External Ear", "tumor of the external Ear", "Neoplasm of the External Ear", "neoplasm of the external Ear", "external ear neoplasm (disease)", "Tumor of external ear (disorder)", "External Auditory Canal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "external ear neoplasm", "shortest_name_length": 18}
{"curie": "MONDO:0021303", "names": ["Small Bowel Adenoma", "small bowel adenoma", "Non-Ampullary Adenoma", "Adenoma of Small Bowel", "adenoma of small bowel", "small intestine adenoma", "Small Intestinal Adenoma", "small intestinal adenoma", "Adenoma of the Small Bowel", "Adenoma of small intestine", "Adenoma of Small Intestine", "adenoma of the small bowel", "adenoma of small intestine", "Adenoma of the Small Intestine", "adenoma of the small intestine", "Adenoma of small intestine (disorder)", "adenoma of small intestine (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenoma of small intestine", "shortest_name_length": 19}
{"curie": "UMLS:C5667240", "names": ["Metastatic Pleomorphic Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Pleomorphic Liposarcoma", "shortest_name_length": 34}
{"curie": "UMLS:C4727842", "names": ["Recurrent Ovarian Cystadenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Ovarian Cystadenocarcinoma", "shortest_name_length": 36}
{"curie": "UMLS:C2363895", "names": ["Recurrent Breast Sarcoma", "Breast sarcoma recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast sarcoma recurrent", "shortest_name_length": 24}
{"curie": "UMLS:C1709166", "names": ["ADENOMA, C-CELL, BENIGN", "Parafollicular Cell Adenoma", "C-cell hyperplasia neoplastic", "Neoplastic C-Cell Hyperplasia", "stage 0 medullary thyroid carcinoma in situ"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplastic C-Cell Hyperplasia", "shortest_name_length": 23}
{"curie": "MONDO:0006491", "names": ["Breisky", "Leukokraurosis", "Kraurosis vulvae", "Kraurosis Vulvae", "kraurosis vulvae", "vulva; kraurosis", "vulvae; kraurosis", "Breisky's disease", "vulva leukoplakia", "leucoplakia vulva", "kraurosis; vulvae", "Vulvae, Kraurosis", "leukoplakia vulva", "Breisky's Disease", "vulval leukoplakia", "kraurosis of vulva", "VULVAR LEUKOPLAKIA", "Vulval Leukoplakia", "Vulval leukoplakia", "vulva; leukoplakia", "leukoplakia; vulva", "VULVAL LEUKOPLAKIA", "Kraurosis of vulva", "leukoplakias vulval", "Leucoplakia of Vulva", "leukoplakia of vulva", "Leukoplakia of vulva", "Leucoplakia of vulva", "Leukoplakic vulvitis", "leukokraurosis vulvae", "leukoplakic; vulvitis", "vulvitis; leukoplakic", "Vulva Lichen Sclerosus", "vulvar lichen sclerosus", "Vulvar Lichen Sclerosus", "Sclerosus, Vulvar Lichen", "Lichen Sclerosus, Vulvar", "lichen sclerosus of vulva", "Lichen Sclerosus of Vulva", "Lichen sclerosus of vulva", "kraurosis of vulva (diagnosis)", "Leukoplakia of vulva (disorder)", "leukoplakia of vulva (diagnosis)", "Lichen sclerosus of female genitalia", "Lichen sclerosus of vulva (disorder)", "Lichen sclerosus et atrophicus of the vulva", "Lichen sclerosus of female external genitalia", "mammalian vulva lichen sclerosus et atrophicus", "Lichen sclerosus of female genitalia (diagnosis)", "lichen sclerosus et atrophicus of mammalian vulva", "inflammatory disease lichen sclerosus of female genitalia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar lichen sclerosus", "shortest_name_length": 7}
{"curie": "MONDO:0006389", "names": ["Prostate Rhabdomyosarcoma", "prostate rhabdomyosarcoma", "rhabdomyosarcoma of prostate", "Rhabdomyosarcoma of Prostate", "prostate gland rhabdomyosarcoma", "rhabdomyosarcoma of the prostate", "Rhabdomyosarcoma of the Prostate", "Rhabdomyosarcoma of the prostate", "rhabdomyosarcoma of prostate (diagnosis)", "prostate gland rhabdomyosarcoma (disease)", "rhabdomyosarcoma (disease) of prostate gland", "prostate gland neoplasm malignant rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate rhabdomyosarcoma", "shortest_name_length": 25}
{"curie": "MONDO:0019605", "names": ["immunotactoid or fibrillary glomerulopathy", "Immunotactoid or fibrillary glomerulonephritis", "fibrillary glomerulonephritis and immunotactoid glomerulopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunotactoid or fibrillary glomerulopathy", "shortest_name_length": 42}
{"curie": "MONDO:0015270", "names": ["BCHED", "Acholinesterasemia", "ACHOLINESTERASEMIA", "apnea, postanesthetic", "Apnea, Postanesthetic", "APNEA, POSTANESTHETIC", "Suxamethonium paralysis", "pseudocholinesterase E1", "Suxamethonium sensitivity", "Suxamethonium Sensitivity", "cholinesterase deficiency", "SUXAMETHONIUM SENSITIVITY", "Cholinesterase 2 Deficiency", "cholinesterase 2 deficiency", "Succinylcholine Sensitivity", "succinylcholine sensitivity", "Succinylcholine sensitivity", "Serum cholinesterase defect", "Serum cholinesterase deficiency", "PSEUDOCHOLINESTERASE DEFICIENCY", "Pseudocholinesterase deficiency", "pseudocholinesterase deficiency", "Plasma cholinesterase deficiency", "Butyrylcholinesterase deficiency", "butyrylcholinesterase deficiency", "pseudocholinesterase; deficiency", "BUTYRYLCHOLINESTERASE DEFICIENCY", "plasma cholinesterase deficiency", "deficiency; pseudocholinesterase", "Pseudocholinesterase E1 deficiency", "Deficiency of butyrylcholinesterase", "Acylcholine acylhydrolase deficiency", "Deficiency of butyrylcholine esterase", "Succinylcholine sensitivity (finding)", "Pseudocholinesterase deficiency syndrome", "pseudocholinesterase deficiency (diagnosis)", "Deficiency of butyrylcholinesterase (disorder)", "HYPOCHOLINESTERASEMIA, FLUORIDE-RESISTANT, JAPANESE TYPE", "Hypocholinesterasemia, Fluoride-Resistant, Japanese Type", "hypocholinesterasemia, fluoride-resistant, Japanese type", "apnea, postanesthetic, susceptibility to, due to BCHE deficiency", "BUTYRYLCHOLINESTERASE DEFICIENCY, FLUORIDE-RESISTANT, JAPANESE TYPE", "Butyrylcholinesterase Deficiency, Fluoride-Resistant, Japanese Type", "butyrylcholinesterase deficiency, fluoride-resistant, Japanese type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "butyrylcholinesterase deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C1332057", "names": ["AIDS-Related Plasmablastic Lymphoma of Oral Mucosa", "AIDS-Related Plasmablastic Lymphoma of the Oral Mucosa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Plasmablastic Lymphoma of the Oral Mucosa", "shortest_name_length": 50}
{"curie": "MONDO:0001008", "names": ["Blepharophimoses", "Blepharophimosis", "blepharophimosis", "blepharophimosis (disease)", "blepharophimosis was observed", "Narrow opening between the eyelids", "blepharophimosis (physical finding)", "Decreased width of palpebral fissure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blepharophimosis", "shortest_name_length": 16}
{"curie": "MONDO:0010888", "names": ["adenomyosis", "Adenomyosis", "ADENOMYOSIS", "Adenomyoses", "Adenomyosis NOS", "uteri adenomyosis", "Adenomyosis uteri", "adenomyosis uteri", "adenomyosis uterus", "uterus adenomyosis", "uterine Adenomyosis", "Uterine Adenomyosis", "UTERUS, ADENOMYOSIS", "uterine adenomyosis", "Uterine adenomyosis", "endometriosis uterus", "uterus endometriosis", "endometriosis interna", "uterine endometriosis", "endometriosis; uterus", "uterus; endometriosis", "adenomyosis of uterus", "Endometriosis interna", "Adenomyosis of Uterus", "Adenomyosis of uterus", "endometriosis internal", "Endometriosis internal", "Internal endometriosis", "endometriosis of uterus", "ENDOMETRIOSIS, INTERNAL", "Endometriosis, internal", "Endometriosis of uterus", "endometriosis, myometrium", "Uterus Corpus Adenomyosis", "adenomyosis of the uterus", "Adenomyosis of the uterus", "uterus corpus adenomyosis", "Endometriosis, myometrium", "Adenomyosis of the Uterus", "uterine corpus adenomyosis", "Uterine Corpus Adenomyosis", "Endometriosis of myometrium", "endometriosis of myometrium", "Endometriosis of uterus, NOS", "internal uterine endometriosis", "uterine endometriosis, internal", "Endometriosis interna (disorder)", "Adenomyosis of uterus (disorder)", "adenomyosis of uterus (diagnosis)", "myometrium endometriosis (disease)", "Endometriosis of uterus (disorder)", "endometriosis of uterus (diagnosis)", "endometriosis (disease) of myometrium", "Endometriosis of myometrium (disorder)", "endometriosis of myometrium (diagnosis)", "internal uterine endometriosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenomyosis", "shortest_name_length": 11}
{"curie": "UMLS:C0686288", "names": ["Carcinoma in situ;breast;F", "Female Breast Carcinoma In Situ", "Carcinoma in situ of female breast", "carcinoma in situ of the female breast", "Carcinoma in situ of female breast, NOS", "Carcinoma in situ of female breast (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carcinoma in situ of female breast", "shortest_name_length": 26}
{"curie": "UMLS:C3897229", "names": ["Untreated Gliosarcoma", "Untreated Childhood Gliosarcoma", "untreated childhood gliosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Untreated Childhood Gliosarcoma", "shortest_name_length": 21}
{"curie": "UMLS:C1334547", "names": ["Major Salivary Gland Adenocarcinoma", "Adenocarcinoma of Major Salivary Gland", "Adenocarcinoma of the Major Salivary Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Major Salivary Gland Adenocarcinoma", "shortest_name_length": 35}
{"curie": "MONDO:0004728", "names": ["diabetic macular edema", "edema diabetic macular", "Diabetic macular edema", "Diabetic macular oedema", "diabetic macular oedema", "Macular edema due to diabetes mellitus", "Macular oedema due to diabetes mellitus", "Macular edema due to diabetes mellitus (disorder)", "diabetes with diabetic retinopathy with macular edema", "diabetes with diabetic retinopathy with macular edema (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diabetic macular edema", "shortest_name_length": 22}
{"curie": "UMLS:C1112346", "names": ["Prostate induration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate induration", "shortest_name_length": 19}
{"curie": "MONDO:0019369", "names": ["CRPS", "Algodystrophy", "reflex sympathetic dystrophy", "Complex regional pain syndrome", "pain regional complex syndrome", "Complex Regional Pain Syndrome", "complex regional pain syndrome", "regional complex pain syndrome", "complex pain regional syndrome", "complex regional pain syndromes", "Complex Regional Pain Syndromes", "Complex regional pain syndromes", "complexed pain regional syndrome", "Pain Syndromes, Regional Complex", "Complex regional pain syndrome NOS", "CRPS - complex regional pain syndrome", "CRPS (Complex Regional Pain Syndromes)", "Complex regional pain syndrome (disorder)", "Complex regional pain syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complex regional pain syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0100365", "names": ["mucopolysaccharidosis or mucopolysaccharidosis-like disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucopolysaccharidosis or mucopolysaccharidosis-like disorder", "shortest_name_length": 60}
{"curie": "MONDO:0006794", "names": ["Hypersensitivity Vasculitis", "VASCULITIS LEUKOCYTOCLASTIC", "LEUKOCYTOCLASTIC VASCULITIS", "Leukocytoclastic vasculitis", "leukocytoclastic vasculitis", "hypersensitivity vasculitis", "Leucocytoclastic vasculitis", "Leukocytoclastic Vasculitis", "leukocytoclastic vasculitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypersensitivity vasculitis", "shortest_name_length": 27}
{"curie": "UMLS:C0264936", "names": ["pulmonary hypertension secondary", "Secondary pulmonary hypertension", "Pulmonary hypertension secondary", "secondary pulmonary hypertension", "hypertension pulmonary secondary", "PULMONARY HYPERTENSION SECONDARY", "Secondary Pulmonary Hypertension", "Pulmonary hypertension, secondary", "Hypertension, pulmonary, secondary", "Secondary pulmonary hypertension (disorder)", "secondary pulmonary hypertension (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary pulmonary hypertension", "shortest_name_length": 32}
{"curie": "UMLS:C5446519", "names": ["Refractory Ampulla of Vater Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Ampulla of Vater Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0018562", "names": ["genetic otorhinolaryngological malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genetic otorhinolaryngological malformation", "shortest_name_length": 43}
{"curie": "MONDO:0011696", "names": ["UVM2", "melanoma, uveal, susceptibility to, 2", "MELANOMA, UVEAL, SUSCEPTIBILITY TO, 2", "melanoma, uveal, susceptibility to, type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melanoma, uveal, susceptibility to, 2", "shortest_name_length": 4}
{"curie": "MONDO:0012845", "names": ["IBD19", "Inflammatory Bowel Disease 19", "inflammatory bowel disease 19", "IRGM inflammatory bowel disease", "inflammatory bowel disease type 19", "inflammatory bowel disease (Crohn disease) 19", "INFLAMMATORY BOWEL DISEASE (CROHN DISEASE) 19", "inflammatory bowel disease caused by mutation in IRGM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory bowel disease 19", "shortest_name_length": 5}
{"curie": "UMLS:C0242648", "names": ["Maternal Transmission", "transmission vertical", "vertical transmission", "Vertical Disease Transmission", "Vertical Pathogen Transmission", "Vertical Infection Transmission", "Pathogen Transmission, Vertical", "Transmission, Vertical Pathogen", "Vertical infection transmission", "Infection Transmission, Vertical", "Transmission, Vertical Infection", "Vertical Infectious Disease Transmission", "Infectious Disease Transmission, Vertical", "Vertical Transmission of Infectious Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vertical Disease Transmission", "shortest_name_length": 21}
{"curie": "MONDO:0017242", "names": ["CCV", "cutaneus colagenous vasculopathy", "cutaneous collagenous vasculopathy", "Cutaneous collagenous vasculopathy", "Cutaneous collagenous vasculopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous collagenous vasculopathy", "shortest_name_length": 3}
{"curie": "UMLS:C0280386", "names": ["nasopharynx squamous cell carcinoma, recurrent", "Nasopharyngeal squamous cell carcinoma recurrent", "Recurrent Nasopharyngeal Squamous Cell Carcinoma", "nasopharyngeal squamous cell carcinoma, recurrent", "epidermoid carcinoma of the nasopharynx, recurrent", "recurrent squamous cell carcinoma of the nasopharynx", "squamous cell carcinoma of the nasopharynx, recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasopharyngeal squamous cell carcinoma recurrent", "shortest_name_length": 46}
{"curie": "MONDO:0023607", "names": ["Laurence Prosser Rocker syndrome", "Laurence-Prosser-Rocker syndrome", "Hirschsprung's disease associated with congenital heart malformation, broad big toes, and ulnar polydactyly", "Hirschsprung's disease associated with ulnar polydactyly, polysyndactyly of big toes and ventricular septal defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laurence-Prosser-Rocker syndrome", "shortest_name_length": 32}
{"curie": "UMLS:C1720802", "names": ["Refsum Disease, Phytanic Acid Oxidase Deficiency", "Refsum Disease, Phytanoyl CoA Hydroxylase Deficiency", "Refsum Disease, Phytanoyl-CoA Hydroxylase Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refsum Disease, Phytanoyl-CoA Hydroxylase Deficiency", "shortest_name_length": 48}
{"curie": "UMLS:C4725845", "names": ["Metastatic Gastroesophageal Junction Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Gastroesophageal Junction Adenocarcinoma", "shortest_name_length": 51}
{"curie": "MONDO:0022538", "names": ["GINGIVAL LEUKOPLAKIA", "gingival leukoplakia", "Gingival Leukoplakia", "Leukoplakia of Gingiva", "leukoplakia of gingiva", "Leukoplakia of gingiva", "Leucoplakia of gingiva", "gingiva oral leukoplakia", "oral leukoplakia of gingiva", "Leukoplakia of gingiva (disorder)", "oral leukoplakia of gingiva (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukoplakia of gingiva", "shortest_name_length": 20}
{"curie": "MONDO:0030986", "names": ["ABOLM", "BLISTERING, ACANTHOLYTIC, OF ORAL AND LARYNGEAL MUCOSA", "blistering, acantholytic, of oral and laryngeal mucosa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blistering, acantholytic, of oral and laryngeal mucosa", "shortest_name_length": 5}
{"curie": "MONDO:0030028", "names": ["CONATOC", "NEURODEGENERATION, CHILDHOOD-ONSET, WITH ATAXIA, TREMOR, OPTIC ATROPHY, AND COGNITIVE DECLINE", "neurodegeneration, childhood-onset, with ataxia, tremor, optic atrophy, and cognitive decline"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodegeneration, childhood-onset, with ataxia, tremor, optic atrophy, and cognitive decline", "shortest_name_length": 7}
{"curie": "MONDO:0005940", "names": ["Respirovirus Infections", "infections, Respirovirus", "Infections, Respirovirus", "Disease due to Respirovirus", "Disease caused by Respirovirus", "Respirovirus infectious disease", "respirovirus infectious disease", "Disease caused by Respirovirus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "respirovirus infectious disease", "shortest_name_length": 23}
{"curie": "MONDO:0010186", "names": ["VDDR2a", "VDDR2A", "Pddr 2A", "PDDR IIA", "rickets-alopecia syndrome", "Rickets-Alopecia Syndrome", "RICKETS-ALOPECIA SYNDROME", "Rickets - alopecia syndrome", "Vitamin D Dependent Rickets 2a", "vitamin D dependent rickets 2a", "vitamin D-dependent rickets type 2A", "Pseudovitamin D-deficiency, type 2A", "vitamin D-dependent rickets, type 2A", "VITAMIN D-DEPENDENT RICKETS, TYPE 2A", "PSEUDOVITAMIN D-DEFICIENCY, TYPE IIA", "Vitamin D-dependent rickets type IIa", "Vitamin D-Dependent Rickets, Type 2A", "Pseudovitamin D-Deficiency, Type IIA", "vitamin D receptor deficiency rickets", "Vitamin D Receptor Deficiency Rickets", "rickets, vitamin D-resistant, type IIA", "rickets, hereditary vitamin D-resistant", "VDR vitamin D-dependent rickets, type 2", "hypocalcemic vitamin D-resistant rickets", "VDDR IIa - Vitamin D-dependent rickets IIa", "vitamin d-dependent rickets type II with alopecia", "Vitamin D-dependent rickets type II with alopecia", "generalized resistance to 1,25-dihydroxyvitamin D", "Vitamin D-dependent rickets type II with alopecia (disorder)", "vitamin D-dependent rickets, type 2 caused by mutation in VDR", "VITAMIN D-DEPENDENT RICKETS, TYPE 2A, WITH OR WITHOUT ALOPECIA", "vitamin D-dependent rickets, type 2A, with or without alopecia", "vitamin D-resistant rickets with end-organ unresponsiveness to 1,25-dihydroxycholecalciferol", "hereditary 1,25 dihydroxyvitamin D-resistant rickets with abnormal vitamin D receptor with alopecia", "Hereditary 1,25 Dihydroxyvitamin D-Resistant Rickets with Abnormal Vitamin D Receptor with Alopecia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitamin D-dependent rickets, type 2A", "shortest_name_length": 6}
{"curie": "MONDO:0005093", "names": ["DERMATOSIS", "Dermopathy", "dermatosis", "dermatoses", "DERMOPATHY", "dermopathy", "Dermatoses", "Dermatosis", "Skin Disease", "disease skin", "Skin disease", "Disease;skin", "Dermatopathy", "skin disease", "anomaly; skin", "skin diseases", "skin disorder", "Skin diseases", "disorder skin", "Skin Diseases", "skin; anomaly", "Skin disorder", "SKIN DISORDER", "Skin Disorder", "diseases skin", "skin disorders", "Dermatosis NOS", "disorders skin", "skin; disorder", "Skin Disorders", "Skin--Diseases", "Genodermatosis", "SKIN DISORDERS", "genodermatosis", "skin condition", "disease of skin", "Skin conditions", "skin; deformity", "of skin disease", "Dermatosis, NOS", "deformity; skin", "Skin Conditions", "Disorder of Skin", "skin abnormality", "Other dermatoses", "Skin Abnormality", "Skin abnormality", "disorder of skin", "abnormality skin", "Disorder of skin", "Abnormality, Skin", "malformation skin", "SKIN MALFORMATION", "Skin disorder NOS", "Skin malformation", "cutaneous disorder", "Skin Abnormalities", "Cutaneous Disorder", "Skin disorder, NOS", "malformations skin", "skin abnormalities", "DISORDER SKIN (NOS)", "Cutaneous disorders", "Skin--Abnormalities", "SKIN DISORDER (NOS)", "Cutaneous Disorders", "Abnormalities, Skin", "Disease of skin, NOS", "zone of skin disease", "dermatologic disease", "Dermatologic disease", "dermatologic diseases", "Iatrogenic dermatosis", "disease integumentary", "integumentary disease", "Dermatologic Disorder", "dermatologic condition", "Dermatologic disorders", "Dermatological disease", "dermatological disease", "diseases integumentary", "disease disorders skin", "Dermatological disorder", "disease of zone of skin", "Congenital anomaly;skin", "dermatological diseases", "skin disorder diagnosis", "diseases disorders skin", "Abnormality of the skin", "Congenital skin disorder", "congenital skin disorder", "disorder of zone of skin", "Congenital Skin Disorder", "dermatological disorders", "Congenital skin anomalies", "congenital anomaly (skin)", "congenital disorders skin", "Congenital anomaly of skin", "skin disorders (diagnosis)", "disease (or disorder); skin", "Disease or syndrome of skin", "Disorder of skin (disorder)", "Congenital cutaneous anomaly", "congenital anomalies of skin", "Diseases and Syndromes of Skin", "Congenital anomaly of skin, NOS", "Congenital integument anomalies", "Skin Diseases and Manifestations", "zone of skin disease or disorder", "CONGENITAL ANOMALIES OF THE SKIN", "skin diseases and manifestations", "Congenital cutaneous anomaly, NOS", "Congenital Abnormality of the Skin", "Cutaneous malformation, congenital", "dermatologic condition (diagnosis)", "Congenital Cutaneous Malformations", "disease or disorder of zone of skin", "Congenital malformation of the skin", "skin and subcutaneous tissue disease", "Congenital anomaly of integument, NOS", "Congenital anomaly of skin (disorder)", "Congenital deformity of integument, NOS", "congenital anomalies of skin (diagnosis)", "Congenital malformation of skin, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin disorder", "shortest_name_length": 10}
{"curie": "MONDO:0014007", "names": ["AGS6", "AICARDI-GOUTIERES SYNDROME 6", "Aicardi-Goutieres syndrome 6", "ADAR Aicardi-Goutieres syndrome", "Adar Aicardi-Goutieres syndrome", "Aicardi-Goutieres syndrome type 6", "Aicardi-Goutieres syndrome caused by mutation in Adar", "Aicardi-Goutieres syndrome caused by mutation in ADAR"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aicardi-Goutieres syndrome 6", "shortest_name_length": 4}
{"curie": "UMLS:C2609260", "names": ["Caudal dysplasia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Caudal dysplasia syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0044329", "names": ["OI18", "osteogenesis imperfecta type 18", "osteogenesis imperfecta, type 18", "osteogenesis imperfecta, type XVIII", "OSTEOGENESIS IMPERFECTA, TYPE XVIII"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteogenesis imperfecta, type 18", "shortest_name_length": 4}
{"curie": "MONDO:0000975", "names": ["Spermatic Cord Lipoma", "spermatic cord lipoma", "spermatic cord; lipoma", "lipoma; spermatic cord", "Lipoma of Spermatic Cord", "Lipoma of spermatic cord", "lipoma of spermatic cord", "lipoma of the spermatic cord", "Lipoma of the spermatic cord", "Lipoma of the Spermatic Cord", "Lipoma of spermatic cord (disorder)", "benign lipoma of the spermatic cord", "benign lipoma of the spermatic cord (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lipoma of spermatic cord", "shortest_name_length": 21}
{"curie": "MONDO:0019215", "names": ["classic organic aciduria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "classic organic aciduria", "shortest_name_length": 24}
{"curie": "UMLS:C5236959", "names": ["Unresectable Periampullary Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Periampullary Adenocarcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0016349", "names": ["HYC3", "Primary hydrocephaly", "Primary hydrocephalus", "newborn; hydrocephalus", "hydrocephalus; newborn", "Congenital hydrocephaly", "congenital hydrocephaly", "Congenital Hydrocephalus", "Congenital hydrencephaly", "HYDROCEPHALUS CONGENITAL", "hydrocephalus congenital", "congenital hydrocephalus", "Hydrocephalus congenital", "Hydrocephalus in newborn", "hydrocephalus in newborn", "Congenital hydrocephalus", "Hydrocephalus, congenital", "Congenital hydrencephalus", "Hydrocephalus, Congenital", "congenital; hydrocephalus", "hydrocephalus; congenital", "Congenital hydrocephalus (disorder)", "congenital hydrocephalus (diagnosis)", "Congenital hydrocephalus, unspecified", "ventricle; dilatation, cerebral, congenital", "Congenital dilatation of cerebral ventricles"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital hydrocephalus", "shortest_name_length": 4}
{"curie": "UMLS:C0577631", "names": ["Carotid Atherosclerosis", "Carotid Atheroscleroses", "Carotid atherosclerosis", "carotid atherosclerosis", "carotid artery atheroma", "Carotid artery atheroma", "Carotid arteriosclerosis", "atheroma; carotid artery", "carotid artery atherosclerosis", "CAROTID ATHEROSCLEROTIC DISEASE", "Carotid Atherosclerotic Disease", "Atherosclerotic Disease, Carotid", "Carotid Atherosclerotic Diseases", "Atherosclerotic Diseases, Carotid", "Carotid atherosclerosis (disorder)", "carotid artery atherosclerosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carotid Atherosclerosis", "shortest_name_length": 23}
{"curie": "MONDO:0000762", "names": ["microduplication sydrome", "chromosomal duplication syndrome", "syndrome caused by partial chromosomal duplication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndrome caused by partial chromosomal duplication", "shortest_name_length": 24}
{"curie": "OMIM:606770", "names": ["CAQ5", "ADIPQTL2", "ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 2", "CIRCULATING ADIPONECTIN QUANTITATIVE TRAIT LOCUS ON CHROMOSOME 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 4}
{"curie": "UMLS:C0015404", "names": ["Eye infection bacterial", "Bacterial Eye Infection", "Bacterial eye infection", "eye infection bacterial", "bacterial eye infection", "Bacterial Eye Infections", "bacterial eye infections", "Infection, Bacterial Eye", "Eye Infection, Bacterial", "bacterial eyes infection", "Infections, Bacterial Eye", "Eye Infections, Bacterial", "Bacterial infection of eye", "Bacterial Ocular Infection", "bacterial infection of eye", "Ocular Infection, Bacterial", "Bacterial Ocular Infections", "ocular bacterial infections", "Eye infection bacterial NOS", "Ocular Infections, Bacterial", "Infections, Bacterial Ocular", "Bacterial infection of eye (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eye Infections, Bacterial", "shortest_name_length": 23}
{"curie": "MONDO:0013040", "names": ["AHUS2", "aHUS2", "aHUS with MCP/CD46 anomaly", "AHUS, SUSCEPTIBILITY TO, 2", "AHUS, susceptibility to, 2", "D-HUS with MCP/CD46 anomaly", "atypical HUS with MCP/CD46 anomaly", "susceptibility to atypical hemolytic uremic syndrome 2", "atypical hemolytic-uremic syndrome with MCP/CD46 anomaly", "HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 2", "hemolytic uremic syndrome, atypical, susceptibility to, 2", "hemolytic uremic syndrome, atypical, susceptibility to, type 2", "hemolytic-uremic syndrome without diarrhea with MCP/CD46 anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical hemolytic-uremic syndrome with MCP/CD46 anomaly", "shortest_name_length": 5}
{"curie": "MONDO:0010897", "names": ["SCZD3", "schizophrenia 3", "SCHIZOPHRENIA 3", "SCHIZOPHRENIA 3 (disorder)", "schizophrenia 3 with or without an affective disorder", "SCHIZOPHRENIA 3 WITH OR WITHOUT AN AFFECTIVE DISORDER", "schizophrenia susceptibility locus, chromosome 6-related", "SCHIZOPHRENIA SUSCEPTIBILITY LOCUS, CHROMOSOME 6-RELATED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schizophrenia 3", "shortest_name_length": 5}
{"curie": "MONDO:0018682", "names": ["congenital analgesia with severe intellectual disability", "congenital absence of pain with severe intellectual disability", "congenital insensitivity to pain with severe intellectual disability", "congenital insensitivity to pain with preserved temperature sensation", "congenital insensitivity to pain with severe non-progressive cognitive delay"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital insensitivity to pain with severe intellectual disability", "shortest_name_length": 56}
{"curie": "UMLS:C4525265", "names": ["stage IIIB intrahepatic bile duct cancer", "Stage IIIB Intrahepatic Bile Duct Cancer", "stage IIIB intrahepatic bile duct cancer AJCC v8", "Stage IIIB Intrahepatic Bile Duct Cancer AJCC v8", "Stage IIIB Intrahepatic Bile Duct Carcinoma AJCC v8", "stage IIIB intrahepatic bile duct carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Intrahepatic Bile Duct Cancer AJCC v8", "shortest_name_length": 40}
{"curie": "UMLS:C1335907", "names": ["Salivary Gland PmA", "Polymorphous adenocarcinoma, classic", "Polymorphous low grade adenocarcinoma", "Salivary Gland Polymorphous Adenocarcinoma", "Salivary Gland Terminal Duct Adenocarcinoma", "Salivary Gland Polymorphous Low Grade Adenocarcinoma", "polymorphous low grade adenocarcinoma of salivary gland", "Polymorphous low grade adenocarcinoma of salivary gland", "polymorphous low-grade adenocarcinoma of salivary gland", "Salivary Gland Polymorphous Adenocarcinoma, Classical Variant", "salivary gland carcinoma polymorphous low-grade adenocarcinoma", "Polymorphous low grade adenocarcinoma of salivary gland (disorder)", "polymorphous low-grade adenocarcinoma of salivary gland (diagnosis)", "polymorphous low grade adenocarcinoma of salivary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Polymorphous low grade adenocarcinoma of salivary gland", "shortest_name_length": 18}
{"curie": "UMLS:C4553413", "names": ["IIB", "Stage IIB Cervical Cancer", "Stage IIB Cervical Cancer AJCC v8", "Stage IIB Cervical Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Cervical Cancer AJCC v8", "shortest_name_length": 3}
{"curie": "UMLS:C0401006", "names": ["Biliary anastomotic leak", "anastomotic leak biliary", "Biliary Anastomotic Leakage", "Biliary anastomotic leak (disorder)", "Biliary anastomotic leak (diagnosis)", "Bile leakage from biliary anastomosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Biliary Anastomotic Leakage", "shortest_name_length": 24}
{"curie": "UMLS:C1707302", "names": ["Heart Synovial Sarcoma", "Cardiac Synovial Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiac Synovial Sarcoma", "shortest_name_length": 22}
{"curie": "EFO:0010060", "names": ["chronic human papillomavirus infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic human papillomavirus infection", "shortest_name_length": 38}
{"curie": "MONDO:0022865", "names": ["corneal dystrophy ichthyosis microcephaly intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal dystrophy ichthyosis microcephaly intellectual disability", "shortest_name_length": 65}
{"curie": "UMLS:C5420301", "names": ["Unresectable Testicular Sarcomatoid Mesothelioma", "Unresectable Paratesticular Sarcomatoid Mesothelioma", "Unresectable Tunica Vaginalis Sarcomatoid Mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Paratesticular Sarcomatoid Mesothelioma", "shortest_name_length": 48}
{"curie": "MONDO:0700036", "names": ["fibrothecoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibrothecoma", "shortest_name_length": 12}
{"curie": "MONDO:0022465", "names": ["anotia facial palsy cardiac defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anotia facial palsy cardiac defect", "shortest_name_length": 34}
{"curie": "MONDO:0022599", "names": ["brachydactyly anonychia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly anonychia", "shortest_name_length": 23}
{"curie": "UMLS:C1707542", "names": ["Cutaneous Chronic Lymphocytic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous Chronic Lymphocytic Leukemia", "shortest_name_length": 38}
{"curie": "UMLS:C4289689", "names": ["Diffuse Laminar Endocervical Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse Laminar Endocervical Hyperplasia", "shortest_name_length": 40}
{"curie": "UMLS:C4521228", "names": ["Refractory Acute Lymphoblastic Leukemia", "Refractory Acute Lymphoblastic Leukemia (ALL)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Acute Lymphoblastic Leukemia", "shortest_name_length": 39}
{"curie": "UMLS:C0033844", "names": ["pseudotumor", "PSEUDOTUMOR", "Pseudotumor", "pseudotumour", "Pseudotumors", "pseudotumors", "Pseudotumour", "Pseudotumor, NOS", "Pseudotumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pseudotumor", "shortest_name_length": 11}
{"curie": "MONDO:0008894", "names": ["CAHMR SYNDROME", "CAHMR syndrome", "cataract-hypertrichosis-mental retardation syndrome", "Cataract, Hypertrichosis, Mental Retardation syndrome", "CATARACT, HYPERTRICHOSIS, MENTAL RETARDATION SYNDROME", "cataract, hypertrichosis, mental retardation syndrome", "Cataract-hypertrichosis-intellectual disability syndrome", "cataract-hypertrichosis-intellectual disability syndrome", "cataract, hypertrichosis, intellectual disability syndrome", "cataract-hypertrichosis-mental retardation (CAHMR) syndrome", "CAHMR (cataract, hypertrichosis, mental retardation) syndrome", "congenital cataract with hypertrichosis and intellectual disability syndrome", "Congenital cataract with hypertrichosis and intellectual disability syndrome", "Congenital cataract with hypertrichosis and intellectual disability syndrome (disorder)", "congenital cataract with hypertrichosis and intellectual disability syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract-hypertrichosis-intellectual disability syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C0267609", "names": ["Squamous Metaplasia of Rectal Mucosa", "Squamous metaplasia of rectal mucosa", "Squamous metaplasia of rectal mucosa (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Squamous metaplasia of rectal mucosa", "shortest_name_length": 36}
{"curie": "UMLS:C0862460", "names": ["Recurrent Ureter Urothelial Cancer", "Urothelial carcinoma ureter recurrent", "Recurrent Ureter Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urothelial carcinoma ureter recurrent", "shortest_name_length": 34}
{"curie": "UMLS:C2987261", "names": ["Esophageal Neuroendocrine Tumor G2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Neuroendocrine Tumor G2", "shortest_name_length": 34}
{"curie": "MONDO:0017013", "names": ["8p trisomy", "trisomy 8p", "Trisomy 8p", "8p+ syndrome", "Duplication 8p", "trisomy type 8p", "dup(8p) syndrome", "8p partial trisomy", "partial trisomy 8p", "Trisomy 8p syndrome", "chromosome 8p trisomy", "8p duplication syndrome", "duplication 8p syndrome", "Chromosome 8, trisomy 8p", "Trisomy 8p syndrome (disorder)", "Trisomy 8p syndrome (diagnosis)", "chromosome 8p duplication syndrome", "anomaly of chromosome 8 partial trisomy short arm trisomy 8p syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trisomy 8p", "shortest_name_length": 10}
{"curie": "MONDO:0024658", "names": ["Extrahepatic Bile Duct Sarcoma", "extrahepatic bile duct sarcoma", "sarcoma of extrahepatic bile duct", "Sarcoma of Extrahepatic Bile Duct", "sarcoma of the extrahepatic bile duct", "Sarcoma of the Extrahepatic Bile Duct", "sarcoma of extrahepatic bile duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extrahepatic bile duct sarcoma", "shortest_name_length": 30}
{"curie": "MONDO:0036990", "names": ["Leydig cell adenoma", "Adenoma, Leydig Cell", "adenoma, interstitial", "Adenoma, Interstitial", "Benign Leydig cell tumor", "Benign Leydig Cell Tumor", "benign Leydig cell tumor", "LEYDIG CELL TUMOR, BENIGN", "Leydig cell tumor, benign", "Benign Leydig cell tumour", "Leydig cell tumour, benign", "Benign Leydig Cell Neoplasm", "benign Leydig cell neoplasm", "Benign Interstitial Cell Tumor", "benign interstitial cell tumor", "Benign interstitial cell tumor", "Benign interstitial cell tumour", "Interstitial cell tumor, benign", "Interstitial cell tumour, benign", "Benign Interstitial Cell Neoplasm", "benign interstitial cell neoplasm", "Leydig cell tumor, benign (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign Leydig cell tumor", "shortest_name_length": 19}
{"curie": "UMLS:C2697566", "names": ["Head and Neck Fistula"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Head and Neck Fistula", "shortest_name_length": 21}
{"curie": "UMLS:C0751110", "names": ["Single seizure", "Single Seizure", "single seizure", "Single Seizures", "Seizure, Single", "Single seizure (finding)", "single seizure (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Single Seizure", "shortest_name_length": 14}
{"curie": "MONDO:0007299", "names": ["SOTOS1", "Sotos syndrome", "Sotos syndrome 1", "cerebral gigantism", "NSD1 Sotos syndrome", "Sotos syndrome type 1", "chromosome 5Q35 deletion syndrome", "Sotos syndrome caused by mutation in NSD1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sotos syndrome 1", "shortest_name_length": 6}
{"curie": "MONDO:0001717", "names": ["Posterior corneal pigmentation", "posterior corneal pigmentation", "Posterior corneal pigmentations", "posterior corneal pigmentations", "Posterior corneal pigmentation (disorder)", "Posterior corneal pigmentations (diagnosis)", "posterior corneal pigmentation (physical finding)", "corneal pigmentations and deposits posterior pigmentation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "posterior corneal pigmentation", "shortest_name_length": 30}
{"curie": "UMLS:C1518701", "names": ["Ovarian Dermoid Cyst with Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Dermoid Cyst with Melanoma", "shortest_name_length": 34}
{"curie": "UMLS:C4553702", "names": ["Stage IIIC Ovarian Cancer", "Stage IIIC Ovarian Cancer AJCC v8", "Stage IIIC Ovarian Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Ovarian Cancer AJCC v8", "shortest_name_length": 25}
{"curie": "UMLS:C5669728", "names": ["Extramedullary Disease in Multiple Myeloma Involving the Skin", "Extramedullary Disease in Plasma Cell Myeloma Involving the Skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extramedullary Disease in Plasma Cell Myeloma Involving the Skin", "shortest_name_length": 61}
{"curie": "UMLS:C0334001", "names": ["atypical glandular hyperplasia", "Atypical glandular hyperplasia", "Atypical Glandular Hyperplasia", "Atypical adenomatous hyperplasia", "atypical adenomatous hyperplasia", "Atypical glandular hyperplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypical adenomatous hyperplasia", "shortest_name_length": 30}
{"curie": "MONDO:0013954", "names": ["IMD29", "IL12B DEFICIENCY", "IL12B deficiency", "IMMUNODEFICIENCY 29", "immunodeficiency 29", "immunodeficiency type 29", "immunodeficiency 29, mycobacteriosis", "MSMD due to complete IL12B deficiency", "MSMD due to complete interleukin 12B deficiency", "Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency", "Mendelian susceptibility to mycobacterial diseases due to complete interleukin 12B deficiency", "IL12B autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency", "autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency caused by mutation in IL12B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C3272334", "names": ["Colorectal Peutz-Jeghers Polyp", "Large Intestinal Peutz-Jeghers Polyp"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Peutz-Jeghers Polyp", "shortest_name_length": 30}
{"curie": "EFO:1001393", "names": ["Periodontal Pocket"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Periodontal Pocket", "shortest_name_length": 18}
{"curie": "MONDO:0001157", "names": ["Personality;passive", "passive personality", "Passive personality", "Dependent personality", "dependent personality", "dependent personalities", "Passive-dependent personality", "Passive-Dependent Personality", "Passive Dependent Personality", "dependent disorder personality", "dependent personality disorder", "Dependent Personality Disorder", "Dependent personality disorder", "Personality, Passive-Dependent", "PERSONALITY DISORDER DEPENDENT", "Disorder, Dependent Personality", "dependent; personality disorder", "personality disorder; dependent", "Dependent Personality Disorders", "dependent personality disorders", "Personality Disorder, Dependent", "Dependent personality disorder (disorder)", "dependent personality disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dependent personality disorder", "shortest_name_length": 19}
{"curie": "MONDO:0000956", "names": ["small bowel tumors", "Small bowel cancer", "small bowel cancer", "bowel cancer small", "SMALL BOWEL CANCER", "cancer small intestine", "cancer intestine small", "Small Intestine Cancer", "Small intestine cancer", "small intestine cancer", "cancer intestines small", "cancers intestines small", "cancer of small intestine", "malignant small bowel tumor", "Malignant Small Bowel Tumor", "Malignant Tumor of Small Bowel", "Malignant tumor of small bowel", "Neoplasm malig;intestine;small", "malignant small bowel neoplasm", "Malignant Small Bowel Neoplasm", "malignant tumor of small bowel", "Malignant tumour of small bowel", "Malignant Small Intestine Tumor", "malignant small intestine tumor", "malignant neoplasm of small bowel", "Malignant Neoplasm of Small Bowel", "Malignant Small Intestine Neoplasm", "Malignant Tumor of the Small Bowel", "malignant tumor of the small bowel", "Malignant tumor of small intestine", "malignant small intestine neoplasm", "Malignant Tumor of Small Intestine", "malignant tumor of small intestine", "Malignant Small Intestinal Neoplasm", "Malignant tumour of small intestine", "malignant small intestinal neoplasm", "Small intestinal neoplasms malignant", "malignant neoplasm of small intestine", "Malignant Neoplasm of Small Intestine", "malignant neoplasm of the small bowel", "Malignant neoplasm of small intestine", "Malignant Neoplasm of the Small Bowel", "Malignant Tumor of the Small Intestine", "malignant tumor of the small intestine", "Malignant small intestinal neoplasm NOS", "Malignant Neoplasm of the Small Intestine", "malignant neoplasm of the small intestine", "malignant neosplasm of the small intestine", "malignant neoplasms of the small intestine", "Malignant neoplasm of small intestine, NOS", "Malignant tumor of small intestine (disorder)", "malignant neoplasm of small intestine (diagnosis)", "Malignant neoplasm of small intestine, unspecified", "Malignant neoplasm of small intestine, unspecified site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small intestine cancer", "shortest_name_length": 18}
{"curie": "UMLS:C1519929", "names": ["Vaginal Small Cell Carcinoma", "Vaginal Small Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Small Cell Neuroendocrine Carcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0016018", "names": ["Diabetic Embryopathy", "diabetic embryopathy", "Diabetic embryopathy", "Diabetic embryopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diabetic embryopathy", "shortest_name_length": 20}
{"curie": "UMLS:C1608955", "names": ["Mycobacterium abscessus Infection", "Mycobacterium abscessus infection", "Infection, Mycobacterium abscessus", "Mycobacterium abscessus Infections", "Infections, Mycobacterium abscessus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mycobacterium abscessus Infection", "shortest_name_length": 33}
{"curie": "UMLS:C0151445", "names": ["Primary Raynaud's", "Primary Raynaud Disease", "Primary Raynaud's Disease", "Primary Raynaud Phenomenon", "Primary Raynaud's phenomenon", "Primary Raynaud's Phenomenon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Raynaud Phenomenon", "shortest_name_length": 17}
{"curie": "MONDO:0008694", "names": ["pseudoprogeria syndrome", "Pseudoprogeria Syndrome", "Pseudoprogeria syndrome", "PSEUDOPROGERIA SYNDROME", "Hal-Berg-Rudolph syndrome", "Hall Berg Rudolph syndrome", "Pseudoprogeria syndrome (disorder)", "Pseudoprogeria syndrome (diagnosis)", "pseudoprogeria/Hallermann-Streiff syndrome", "pseudoprogeria/Hallermann-Streiff syndrome (PHS)", "ABSENT EYEBROWS AND EYELASHES WITH MENTAL RETARDATION", "Absent Eyebrows and Eyelashes with Mental Retardation", "absent eyebrows and eyelashes with mental retardation", "absent eyebrows and eyelashes with intellectual disability", "Absent eyebrows and eyelashes-intellectual disability syndrome", "absent eyebrows and eyelashes-intellectual disability syndrome", "eyebrows and eyelashes absence-intellectual disability syndrome", "Absent eyebrows and eyelashes with intellectual disability syndrome", "mental retardation, absence of eyebrows and eyelashes, progressive spastic quadriplegia, microcephaly, glaucoma, and small, beaked nose", "intellectual disability, absence of eyebrows and eyelashes, progressive spastic quadriplegia, microcephaly, glaucoma, and small, beaked nose"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudoprogeria syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0008719", "names": ["Curran syndrome", "acrorenal syndrome", "acrorenal syndrome recessive", "Acrorenal syndrome recessive", "Acrorenal syndrome autosomal recessive", "autosomal recessive acrorenal syndrome", "acrorenal syndrome autosomal recessive", "acrorenal syndrome, autosomal recessive", "Acrorenal Syndrome, Autosomal Recessive", "ACRORENAL SYNDROME, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acrorenal syndrome, autosomal recessive", "shortest_name_length": 15}
{"curie": "MONDO:0015012", "names": ["MPSPS", "mucopolysaccharidosis-plus syndrome", "MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME", "mucopolysaccharidosis-like plus disease", "mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders", "shortest_name_length": 5}
{"curie": "MONDO:0010012", "names": ["APS2", "PGA 2", "APS 2", "APS II", "PGA II", "Schmidt", "APS type 2", "SCHMIDT SYNDROME", "Schmidt syndrome", "Schmidt Syndrome", "syndrome schmidt", "schmidt syndrome", "Syndrome, Schmidt", "schmidts syndrome", "Schmidt's syndrome", "Schmidt's Syndrome", "schmidt's syndrome", "Syndrome, Schmidt's", "autoimmune polyendocrinopathy type 2", "Autoimmune polyendocrinopathy type 2", "autoimmune polyendocrine syndrome type 2", "autoimmune polyglandular syndrome type 2", "Autoimmune polyglandular syndrome type 2", "Autoimmune Polyglandular Syndrome Type 2", "Autoimmune polyendocrine syndrome type 2", "polyglandular deficiency syndrome type 2", "Autoimmune Polyglandular Syndrome Type II", "Autoimmune polyendocrine syndrome type II", "Polyglandular Autoimmune Syndrome, Type 2", "Polyglandular autoimmune syndrome, type 2", "Polyglandular Deficiency Syndrome, Type 2", "Polyglandular autoimmune syndrome type II", "Polyglandular Type II Autoimmune Syndrome", "autoimmune polyendocrine syndrome type II", "polyglandular autoimmune syndrome, type 2", "Autoimmune Polyendocrine Syndrome, Type 2", "polyendocrine autoimmune syndrome, type 2", "autoimmune polyendocrine syndrome, type II", "Addison's disease with struma lymphomatosa", "Type 2 polyendocrine autoimmunity syndrome", "Autoimmune Syndrome Type II, Polyglandular", "Autoimmune Polyendocrine Syndrome, Type II", "POLYENDOCRINE AUTOIMMUNE SYNDROME, TYPE II", "AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE II", "POLYGLANDULAR AUTOIMMUNE SYNDROME, TYPE II", "Polyendocrine Autoimmune Syndrome, Type II", "Polyglandular autoimmune syndrome - type II", "diabetes mellitus, Addison disease, myxedema", "DIABETES MELLITUS, ADDISON DISEASE, MYXEDEMA", "Diabetes Mellitus, Addison Disease, Myxedema", "multiple endocrine deficiency syndrome, type 2", "diabetes mellitus, Addison's disease, myxedema", "Multiple Endocrine Deficiency Syndrome, Type 2", "Diabetes Mellitus, Addison's Disease, Myxedema", "PGA - Polyglandular autoimmune syndrome - type II", "Diabetes mellitus, Addison's disease and myxedema", "Diabetes mellitus, Addison's disease and myxoedema", "Polyglandular autoimmune syndrome, type 2 (disorder)", "autoimmune polyendocrine syndrome type II (diagnosis)", "Primary hypothyroidism AND adrenocortical insufficiency", "Primary hypothyroidism and adrenocortical insufficiency", "Autoimmune thyroid disease and/or type 1 diabetes-Addison disease syndrome", "autoimmune thyroid disease and/or type 1 diabetes-Addison disease syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune polyendocrinopathy type 2", "shortest_name_length": 4}
{"curie": "MONDO:0006199", "names": ["endometrial undifferentiated carcinoma", "undifferentiated endometrial carcinoma", "Undifferentiated Endometrial Carcinoma", "Endometrial Undifferentiated Carcinoma", "Primary undifferentiated carcinoma of endometrium", "Primary undifferentiated carcinoma of endometrium (disorder)", "Primary undifferentiated carcinoma of endometrium (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometrial undifferentiated carcinoma", "shortest_name_length": 38}
{"curie": "UMLS:C0001956", "names": ["Alcohol Use Disorder", "Alcohol use disorder", "alcohol use disorder", "alcohol use disorders", "Alcohol Use Disorders", "Use Disorders, Alcohol", "Alcohol Use Disorder (AUD)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alcohol Use Disorder", "shortest_name_length": 20}
{"curie": "MONDO:0018784", "names": ["pediatric MS", "MS pediatric", "pediatric multiple sclerosis", "multiple sclerosis, pediatric"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pediatric multiple sclerosis", "shortest_name_length": 12}
{"curie": "MONDO:0014165", "names": ["GPIBD7", "MCAHS3", "PIGT-CDG", "M syndrome", "MCAHS type 3", "light fixation seizure syndrome", "glycosylphosphatidylinositol biosynthesis defect 7", "GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 7", "multiple congenital anomalies-hypotonia-seizures syndrome 3", "MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3", "congenital disorder of glycosylation due to PIGT deficiency", "multiple congenital anomalies-hypotonia-seizures syndrome type 3", "PIGT multiple congenital anomalies/dysmorphic syndrome-intellectual disability", "intellectual disability-seizures-hypotonia-ophthalmologic-skeletal anomalies syndrome", "multiple congenital anomalies/dysmorphic syndrome-intellectual disability caused by mutation in PIGT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple congenital anomalies-hypotonia-seizures syndrome 3", "shortest_name_length": 6}
{"curie": "MONDO:0054833", "names": ["CMT2DD", "ATP1A1-related CMT2", "Charcot-Marie-Tooth disease type 2DD", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2DD", "Charcot-Marie-Tooth neuropathy, type 2Dd", "Charcot-Marie-Tooth neuropathy, type 2DD", "charcot-marie-tooth disease, axonal, type 2DD", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2DD", "Charcot-Marie-Tooth disease, axonal, type 2DD", "Charcot-Marie-tooth disease, axonal, type 2DD", "Autosomal dominant Charcot-Marie-Tooth disease type 2DD", "Autosomal dominant Charcot-Marie-Tooth disease type 2DD (disorder)", "ATP1A1-related autosomal dominant Charcot-Marie-Tooth disease type 2", "ATP1A1 (ATPase Na+/K+ transporting subunit alpha 1) related autosomal dominant Charcot-Marie-Tooth disease type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "charcot-marie-tooth disease, axonal, type 2DD", "shortest_name_length": 6}
{"curie": "MONDO:0018837", "names": ["Postinfective vasculitis", "postinfectious vasculitis", "Postinfectious vasculitis", "Post-infectious vasculitis", "Vasculitis due to and following viral infection", "Vasculitis due to and following viral infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postinfectious vasculitis", "shortest_name_length": 24}
{"curie": "UMLS:C3828507", "names": ["Postpartum Obstetric Air Embolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postpartum Obstetric Air Embolism", "shortest_name_length": 33}
{"curie": "MONDO:0011689", "names": ["DYX6", "dyslexia, susceptibility to, 6", "DYSLEXIA, SUSCEPTIBILITY TO, 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyslexia, susceptibility to, 6", "shortest_name_length": 4}
{"curie": "MONDO:0008607", "names": ["Triphalangeal thumbs brachyectrodactyly", "triphalangeal thumbs brachyectrodactyly", "Carnevale Hernandez del Castillo syndrome", "Carnevale-Hernández-del Castillo syndrome", "Triphalangeal Thumbs with Brachyectrodactyly", "triphalangeal thumbs with brachyectrodactyly", "TRIPHALANGEAL THUMBS WITH BRACHYECTRODACTYLY", "triphalangeal thumbs-brachyectrodactyly syndrome", "Triphalangeal thumbs-brachyectrodactyly syndrome", "triphalangeal thumb and brachyectrodactyly syndrome", "Triphalangeal thumb and brachyectrodactyly syndrome", "Triphalangeal thumb with brachyectrodactyly syndrome", "triphalangeal thumb and brachy-ectrodactyly syndrome", "Triphalangeal thumb and brachy-ectrodactyly syndrome", "Triphalangeal thumb with brachyectrodactyly syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "triphalangeal thumbs-brachyectrodactyly syndrome", "shortest_name_length": 39}
{"curie": "MONDO:0018199", "names": ["Norse", "New onset refractory status epilepticus", "new-onset refractory status epilepticus", "De novo cryptogenic refractory multifocal febrile status epilepticus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "new-onset refractory status epilepticus", "shortest_name_length": 5}
{"curie": "UMLS:C1519683", "names": ["Tumor Leakage", "Tumor Spillage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tumor Leakage", "shortest_name_length": 13}
{"curie": "UMLS:C5237210", "names": ["Locally Advanced Laryngeal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Laryngeal Squamous Cell Carcinoma", "shortest_name_length": 50}
{"curie": "MONDO:0600008", "names": ["CRS", "cytokine storm", "Hypercytokinemia", "Hypercytokinemias", "Cytokine Storm Syndrome", "cytokine release syndrome", "Cytokine release syndrome", "Cytokine Release Syndrome", "Cytokine Release Syndromes", "Cytokine-associated toxicity", "cytokine-associated toxicity", "CRS - cytokine release syndrome", "Cytokine release syndrome (diagnosis)", "Cytokine-associated toxicity (disorder)", "infusion reaction cytokine release syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cytokine release syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0004942", "names": ["Orbit Lymphoma", "orbit lymphoma", "lymphoma orbital", "Orbital lymphoma", "orbital lymphoma", "Lymphoma of Orbit", "lymphomas orbital", "lymphoma of orbit", "Lymphoma of the Orbit", "lymphoma of the orbit", "Lymphoma of the orbit", "Primary Orbit Lymphoma", "primary orbit lymphoma", "Primary orbital lymphoma", "primary orbital lymphoma", "Orbital lymphoma (disorder)", "Orbital lymphoma (diagnosis)", "malignant neoplasm lymphoma orbital"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orbit lymphoma", "shortest_name_length": 14}
{"curie": "MONDO:0019822", "names": ["arterial duct anomaly", "patent ductus arteriosus anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arterial duct anomaly", "shortest_name_length": 21}
{"curie": "MONDO:0019443", "names": ["DTGA", "D-TGA", "DTGA1", "isolated ventriculoarterial discordance", "dextro-looped transposition of the great arteries", "congenitally uncorrected transposition of the great vessels", "congenitally uncorrected transposition of the great arteries", "ventriculoarterial discordance with atrioventricular concordance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dextro-looped transposition of the great arteries", "shortest_name_length": 4}
{"curie": "UMLS:C1706724", "names": ["Adrenal Gland Oncocytic Adenoma", "Adrenal Cortex Oncocytic Adenoma", "Adrenal Cortical Oncocytic Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adrenal Cortical Oncocytic Adenoma", "shortest_name_length": 31}
{"curie": "MONDO:0018579", "names": ["disorder of keton body transport", "disorder of ketone body transport"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of ketone body transport", "shortest_name_length": 32}
{"curie": "MONDO:0009446", "names": ["Passwell-Goodman-Siprkowski syndrome", "ichthyosis intellectual deficit dwarfism renal impairment", "ichthyosis, mental retardation, dwarfism and renal impairment", "ICHTHYOSIS, MENTAL RETARDATION, DWARFISM, AND RENAL IMPAIRMENT", "Ichthyosis, mental retardation, dwarfism, and renal impairment", "ichthyosis, mental retardation, dwarfism, and renal impairment", "ichthyosis, intellectual disability, dwarfism and renal impairment", "ichthyosis, intellectual disability, dwarfism, and renal impairment", "ichthyosis-intellectual disability-dwarfism-renal impairment syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ichthyosis-intellectual disability-dwarfism-renal impairment syndrome", "shortest_name_length": 36}
{"curie": "UMLS:C0241424", "names": ["bite tongue", "tongue bite", "TONGUE BITE", "bites tongue", "TONGUE BITING", "Tongue Biting", "tongue biting", "biting tongue", "Tongue-biting", "Tongue biting", "Biting of Tongue", "Tongue biting (disorder)", "Biting of oral mucosa - tongue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tongue biting", "shortest_name_length": 11}
{"curie": "MONDO:0022196", "names": ["varioliform gastritis", "Chronic erosive gastritis", "chronic erosive gastritis", "diffuse varioliform gastritis", "Diffuse varioliform gastritis", "ceg - chronic erosive gastritis", "CEG - Chronic erosive gastritis", "Chronic erosive gastritis (disorder)", "chronic erosive gastritis (diagnosis)", "idiopathic chronic, erosive gastritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic erosive gastritis", "shortest_name_length": 21}
{"curie": "MONDO:0020124", "names": ["Neuromuscular junction disease", "neuromuscular junction disease", "Neuromuscular Junction Disease", "Neuromuscular junction disorder", "Neuromuscular Junction Disorder", "Neuromuscular Junction Diseases", "neuromuscular junction diseases", "neuromuscular junction disorder", "Neuromuscular Junction Disorders", "neuromuscular junction disorders", "Neuromuscular Transmission Disorder", "Neuromuscular Transmission Disorders", "Neuromuscular junction disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuromuscular junction disease", "shortest_name_length": 30}
{"curie": "MONDO:0020815", "names": ["Dentigerous cyst", "Dentigerous Cyst", "dentigerous cyst", "cyst; dentigerous", "dentigerous cysts", "Dentigerous Cysts", "dentigerous; cyst", "Cyst, Dentigerous", "Cysts, Dentigerous", "dentigerous jaw cyst", "Follicular cyst of jaw", "jaw; cyst, dentigerous", "follicular cyst of jaw", "cyst; jaw, dentigerous", "dentigerous cyst of jaw", "Heterotopic polyodontia", "Dentigerous cyst of jaw", "Dentigerous cyst (disorder)", "Dentigerous odontogenic cyst", "dentigerous odontogenic cyst", "Cyst, dentigerous odontogenic", "dentigerous cyst of jaw (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dentigerous cyst", "shortest_name_length": 16}
{"curie": "EFO:0009965", "names": ["Schizoaffective disorder-bipolar type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Schizoaffective disorder-bipolar type", "shortest_name_length": 37}
{"curie": "UMLS:C1335350", "names": ["Parathyroid Clear Cell Hyperplasia", "Clear Cell Hyperplasia of Parathyroid", "Clear Cell Hyperplasia of the Parathyroid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parathyroid Clear Cell Hyperplasia", "shortest_name_length": 34}
{"curie": "MONDO:0011313", "names": ["MPPH", "MPPH1", "MEG-PMG-MEGACC SYNDROME", "Meg-Pmg-Megacc Syndrome", "Meg-PMG-Megacc syndrome", "megalencephaly, polymicrogyria, mega corpus callosum syndrome", "Megalencephaly, Polymicrogyria, Mega Corpus Callosum Syndrome", "MEGALENCEPHALY, POLYMICROGYRIA, MEGA CORPUS CALLOSUM SYNDROME", "Megalancephaly Polymicrogyria-Polydactyly Hydrocephalus Syndrome", "Megalanecephaly Polymicrogyria-Polydactyly Hydrocephalus Syndrome", "MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 1", "megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1", "megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome type 1", "Megalencephaly, Mega Corpus Callosum, And Complete Lack Of Motor Development", "MEGALENCEPHALY, MEGA CORPUS CALLOSUM, AND COMPLETE LACK OF MOTOR DEVELOPMENT", "megalencephaly, mega corpus callosum, and complete lack of motor development", "PIK3R2 megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome", "megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome caused by mutation in PIK3R2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1", "shortest_name_length": 4}
{"curie": "MONDO:0006656", "names": ["Aortitis", "aortitis", "Aortitides", "Aortitis NOS", "Aortitis, NOS", "Aortic vasculitis", "aorta inflammation", "Aortitis (disorder)", "aortitis (diagnosis)", "inflammation of aorta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortitis", "shortest_name_length": 8}
{"curie": "UMLS:C1321523", "names": ["WANDERING PACEMAKER", "Wandering pacemaker", "Wandering Pacemaker", "pacemaker; wandering", "wandering; pacemaker", "Ectopic atrial pacemaker", "Wandering atrial pacemaker", "wandering atrial pacemaker", "Wandering Atrial Pacemaker", "WANDERING ATRIAL PACEMAKER", "ATRIAL PACEMAKER WANDERING", "Wandering atrial pacemaker (finding)", "wandering atrial pacemaker (diagnosis)", "Wandering Atrial Pacemaker by ECG Finding", "Wandering Atrial Pacemaker by EKG Finding"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ectopic atrial pacemaker", "shortest_name_length": 19}
{"curie": "UMLS:C1266075", "names": ["Tawarian Node", "Endodermal Rest", "Benign Mesothelioma of Mahaim", "Intracardiac Endodermal Heterotopia", "Cystic Tumor of Atrioventricular Node", "Mesothelioma of Atrioventricular Node", "Cystic tumor of atrio-ventricular node", "Cystic tumour of atrio-ventricular node", "Cystic Tumor of the Atrioventricular Node", "Cystic tumor of atrio-ventricular node (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cystic tumor of atrio-ventricular node", "shortest_name_length": 13}
{"curie": "UMLS:C4329793", "names": ["Ependymal Tumor of Brain and Spinal Cord"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ependymal Tumor of Brain and Spinal Cord", "shortest_name_length": 40}
{"curie": "UMLS:C2826584", "names": ["Dusky Mucosa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dusky Mucosa", "shortest_name_length": 12}
{"curie": "UMLS:C1514837", "names": ["Renal Cell Carcinoma Associated with t(X;17)(p11.2;q25)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal Cell Carcinoma Associated with t(X;17)(p11.2;q25)", "shortest_name_length": 55}
{"curie": "UMLS:C4724986", "names": ["Refractory Myelodysplastic Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Myelodysplastic Syndrome", "shortest_name_length": 35}
{"curie": "UMLS:C0157997", "names": ["Menopausal arthritis", "menopausal arthritis", "arthritis; menopausal", "Climacteric arthritis", "climacteric arthritis", "menopausal; arthritis", "Arthritis climacteric", "Climacteric Arthritis", "arthritis; climacteric", "Climacteric arthritis (disorder)", "climacteric arthritis (diagnosis)", "Climacteric arthritis, site unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Climacteric arthritis", "shortest_name_length": 20}
{"curie": "UMLS:C1334703", "names": ["Metachronous Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metachronous Malignant Neoplasm", "shortest_name_length": 31}
{"curie": "UMLS:C1142150", "names": ["Autoimmune nephritis", "Nephritis autoimmune"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Autoimmune nephritis", "shortest_name_length": 20}
{"curie": "UMLS:C2983709", "names": ["Hepatocellular Carcinoma by AJCC v6 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatocellular Carcinoma by AJCC v6 Stage", "shortest_name_length": 41}
{"curie": "MONDO:0009965", "names": ["PRLMNS", "Perlman Syndrome", "PERLMAN SYNDROME", "Perlman syndrome", "Perlman syndrome (disorder)", "Perlman nephroblastomatosis syndrome", "Renal Hamartomas, Nephroblastomatosis and Fetal Gigantism", "renal hamartomas, nephroblastomatosis and fetal gigantism", "Renal hamartomas, nephroblastomatosis, and fetal gigantism", "renal hamartomas, nephroblastomatosis, and fetal gigantism", "RENAL HAMARTOMAS, NEPHROBLASTOMATOSIS, AND FETAL GIGANTISM", "fetal gigantism-renal harmatoma-nephroblastomatosis syndrome", "nephroblastomatosis fetal ascites macrosomia and Wilms tumor", "Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor", "nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor", "nephroblastomatosis - fetal ascites - macrosomia - Wilms tumor", "NEPHROBLASTOMATOSIS, FETAL ASCITES, MACROSOMIA, AND WILMS TUMOR", "nephroblastomatosis, fetal ascites, macrosomia, and Wilms tumor", "Nephroblastomatosis, Fetal Ascites, Macrosomia, And Wilms Tumor", "Nephroblastomatosis-fetal ascites-macrosomia-Wilms tumor syndrome", "nephroblastomatosis-fetal ascites-macrosomia-Wilms tumor syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perlman syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C2987255", "names": ["Moderately Differentiated Esophageal Squamous Cell Cancer", "Esophageal Moderately Differentiated Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Moderately Differentiated Squamous Cell Carcinoma", "shortest_name_length": 57}
{"curie": "MONDO:0013261", "names": ["CMD1R", "LVNC4", "dilated cardiomyopathy 1R", "cardiomyopathy, dilated, 1R", "CARDIOMYOPATHY, DILATED, 1R", "dilated cardiomyopathy type 1R", "LEFT VENTRICULAR NONCOMPACTION 4", "left ventricular noncompaction 4", "cardiomyopathy, dilated, type 1R", "ACTC1 familial isolated dilated cardiomyopathy", "familial isolated dilated cardiomyopathy caused by mutation in ACTC1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1R", "shortest_name_length": 5}
{"curie": "MONDO:0013812", "names": ["BRWS2", "Baraitser-Winter syndrome 2", "Baraitser-WINTER syndrome 2", "Baraitser-winter syndrome 2", "BARAITSER-WINTER SYNDROME 2", "Baraitser-Winter syndrome type 2", "ACTG1 Baraitser-Winter cerebrofrontofacial syndrome", "Baraitser-Winter cerebrofrontofacial syndrome caused by mutation in ACTG1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Baraitser-winter syndrome 2", "shortest_name_length": 5}
{"curie": "UMLS:C0242596", "names": ["MRD", "Residual Neoplasm", "residual neoplasm", "Residual Neoplasms", "Neoplasm, Residual", "Residual Minimal Disease", "Minimal Residual Disease", "Minimal residual disease", "minimal residual disease", "Residual Disease, Minimal", "Minimal Disease, Residual", "Minimal Residual Diseases", "Residual Minimal Diseases", "Measurable Residual Disease", "Detectable Residual Disease", "minimal residual disease (MRD)", "remainder of a tumor or cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplasm, Residual", "shortest_name_length": 3}
{"curie": "MONDO:0011018", "names": ["VBS", "DASS", "STHAG6", "STHAG6, FORMERLY", "selective tooth agenesis 5", "VERLOES-BOURGUIGNON SYNDROME", "tooth agenesis, selective, 6", "Verloes Bourguignon syndrome", "Verloes-Bourguignon syndrome", "DENTAL ANOMALIES AND SHORT STATURE", "dental anomalies and short stature", "Platyspondyly amelogenesis imperfecta", "tooth agenesis, selective, 6, formerly", "TOOTH AGENESIS, SELECTIVE, 6, FORMERLY", "amelogenesis imperfecta and platyspondyly", "PLATYSPONDYLY WITH AMELOGENESIS IMPERFECTA", "platyspondyly with amelogenesis imperfecta", "Platyspondyly with amelogenesis imperfecta", "brachyolmia-amelogenesis imperfecta syndrome", "Brachyolmia-amelogenesis imperfecta syndrome", "Platyspondyly-amelogenesis imperfecta syndrome", "platyspondyly-amelogenesis imperfecta syndrome", "Brachyolmia and amelogenesis imperfecta syndrome", "skeletal dysplasia with amelogenesis imperfecta and platyspondyly", "Skeletal dysplasia with amelogenesis imperfecta and platyspondyly", "Autosomal recessive brachyolmia and amelogenesis imperfecta syndrome", "Autosomal recessive brachyolmia and amelogenesis imperfecta syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachyolmia-amelogenesis imperfecta syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0001546", "names": ["coccyx; hypermobility", "hypermobility; coccyx", "hypermobility of coccyx", "Hypermobility of coccyx", "Hypermobility of the coccyx", "hypermobility of the coccyx", "coccygeal hypermobility syndrome", "Coccygeal hypermobility syndrome", "Hypermobility of coccyx (finding)", "hypermobility of coccyx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypermobility of coccyx", "shortest_name_length": 21}
{"curie": "MONDO:0009306", "names": ["CCHIDG", "CID due to RAG 1/2 deficiency", "combined immunodeficiency with granulomatosis", "combined immunodeficiency with skin granulomas", "combined immunodeficiency due to RAG 1/2 deficiency", "combined cellular and humoral immune defects with granulomas", "COMBINED CELLULAR AND HUMORAL IMMUNE DEFECTS WITH GRANULOMAS", "Combined Cellular And Humoral Immune Defects With Granulomas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined immunodeficiency with skin granulomas", "shortest_name_length": 6}
{"curie": "MONDO:0100157", "names": ["IGS2", "Imerslund-Grasbeck syndrome 2", "IMERSLUND-GRASBECK SYNDROME 2", "Imerslund-Grasbeck syndrome type 2", "MEGALOBLASTIC ANEMIA, NORWEGIAN TYPE", "megaloblastic anemia, Norwegian type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Imerslund-Grasbeck syndrome type 2", "shortest_name_length": 4}
{"curie": "MONDO:0005639", "names": ["ARC", "AIDS-like syndrome", "AIDS RELATED COMPLEX", "AIDS Related Complex", "AIDS related complex", "AIDS-Related Complex", "aids-related complex", "AIDS-related complex", "Complex, AIDS-Related", "Lymphadenopathy Syndrome", "Lymphadenopathy Syndromes", "Syndrome, Lymphadenopathy", "AIDS-related complex [ARC]", "aids-related complex (ARC)", "Syndromes, Lymphadenopathy", "acquired immunodeficiency syndrome-like syndrome", "Acquired immune deficiency syndrome-related complex", "ARC - Acquired immunodeficiency syndrome-related complex", "acquired immunodeficiency syndrome-like syndrome (diagnosis)", "Acquired immunodeficiency syndrome-related complex, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS related complex", "shortest_name_length": 3}
{"curie": "MONDO:0100360", "names": ["herpes simplex type 2 infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "herpes simplex type 2 infectious disease", "shortest_name_length": 40}
{"curie": "MONDO:0009621", "names": ["microcephaly-cervical spine fusion anomalies", "Microcephaly cervical spine fusion anomalies", "microcephaly cervical spine fusion anomalies", "Microcephaly with cervical spine fusion anomaly", "MICROCEPHALY WITH CERVICAL SPINE FUSION ANOMALIES", "Microcephaly with Cervical Spine Fusion Anomalies", "microcephaly with cervical spine fusion anomalies", "Microcephaly-cervical spine fusion anomalies syndrome", "microcephaly-cervical spine fusion anomalies syndrome", "Microcephalus co-occurrent with cervical spine fusion anomaly", "Microcephalus co-occurrent with cervical spine fusion anomaly (disorder)", "Microcephaly, mild mental retardation, short stature, and skeletal anomalies", "microcephaly, mild mental retardation, short stature, and skeletal anomalies", "microcephaly-mild mental retardation-short stature-skeletal anomalies syndrome", "microcephaly, mild intellectual disability, short stature, and skeletal anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly-cervical spine fusion anomalies syndrome", "shortest_name_length": 44}
{"curie": "MONDO:0005598", "names": ["dopaminergic neuroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dopaminergic neuroblastoma", "shortest_name_length": 26}
{"curie": "MONDO:0015386", "names": ["Epignathus", "epignathus", "Palatine teratoma", "epignathus (disease)", "Epignathus (disorder)", "Oropharyngeal teratoma", "oropharyngeal teratoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epignathus", "shortest_name_length": 10}
{"curie": "MONDO:0019597", "names": ["46,XY disorder of sex development due to isolated 17,20-lyase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XY disorder of sex development due to isolated 17,20-lyase deficiency", "shortest_name_length": 72}
{"curie": "UMLS:C3273098", "names": ["Gallbladder Mucinous Cystic Neoplasm, Low-Grade", "Gallbladder Mucinous Cystic Neoplasm, Low Grade", "Gallbladder MCN with Low Grade Intraepithelial Neoplasia", "Gallbladder Mucinous Cystic Neoplasm with Low Grade Intraepithelial Neoplasia", "Mucinous cystic neoplasm with low-grade intraepithelial neoplasia of gallbladder", "Mucinous cystic neoplasm with low-grade intraepithelial neoplasia of gallbladder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mucinous cystic neoplasm with low-grade intraepithelial neoplasia of gallbladder", "shortest_name_length": 47}
{"curie": "UMLS:C1708176", "names": ["Gallbladder Papillary Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gallbladder Papillary Adenoma", "shortest_name_length": 29}
{"curie": "UMLS:C3494954", "names": ["Hutch Diverticulum", "Hutch diverticulum", "Hutch diverticulum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hutch diverticulum", "shortest_name_length": 18}
{"curie": "UMLS:C0431122", "names": ["meningioma atypical", "atypical meningioma", "Atypical Meningioma", "Atypical meningioma", "Atypical meningioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypical meningioma", "shortest_name_length": 19}
{"curie": "MONDO:0009752", "names": ["Neuropathy, Painful", "NEUROPATHY, PAINFUL", "neuropathy, painful"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuropathy, painful", "shortest_name_length": 19}
{"curie": "UMLS:C0280337", "names": ["Accessory Sinus Inverted Papilloma", "Paranasal Sinus Inverted Papilloma", "Paranasal Sinus Inverting Papilloma", "Accessory Sinus Inverting Papilloma", "Inverted Papilloma of Accessory Sinus", "Inverted Papilloma of Paranasal Sinus", "Inverting Papilloma of Paranasal Sinus", "Inverting Papilloma of Accessory Sinus", "Inverted Papilloma of the Accessory Sinus", "Inverted Papilloma of the Paranasal Sinus", "Inverting Papilloma of the Paranasal Sinus", "Inverting Papilloma of the Accessory Sinus", "Inverting papilloma of the paranasal sinus", "Paranasal Sinus Inverted Schneiderian Papilloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Inverting papilloma of the paranasal sinus", "shortest_name_length": 34}
{"curie": "MONDO:0019323", "names": ["Senear-Usher", "Usher-Senear", "seborrheic pemphigus", "Seborrheic pemphigus", "Senear-Usher syndrome", "Pemphigus erythematous", "Pemphigus erythematosus", "pemphigus erythematosus", "erythematosus; pemphigus", "pemphigus; erythematosus", "Pemphigus, erythematosus", "Pemphigus erythematosus (disorder)", "pemphigus erythematosus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pemphigus erythematosus", "shortest_name_length": 12}
{"curie": "MONDO:0016451", "names": ["Idiopathic hypersomnia with long sleep time", "idiopathic hypersomnia with long sleep time", "Idiopathic hypersomnia associated with long sleep time", "Idiopathic hypersomnia associated with long sleep time (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic hypersomnia with long sleep time", "shortest_name_length": 43}
{"curie": "MONDO:0012580", "names": ["Congenital PAP", "congenital PAP", "hereditary pulmonary alveolar proteinosis", "Hereditary pulmonary alveolar proteinosis", "Congenital pulmonary alveolar proteinosis", "congenital pulmonary alveolar proteinosis", "Pulmonary alveolar proteinosis, congenital", "pulmonary alveolar proteinosis, congenital", "sufactant metabolism dysfunction, pulmonary", "inborn error of pulmonary surfactant metabolism", "Congenital pulmonary alveolar proteinosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary pulmonary alveolar proteinosis", "shortest_name_length": 14}
{"curie": "MONDO:0006591", "names": ["SUBCUTIS", "subcutis", "Subcutis", "PANNICULITIS", "Panniculitis", "panniculitis", "Panniculitides", "Panniculitis, NOS", "Subcutaneous Tissue", "Subcutaneous tissue", "Panniculitis (disorder)", "panniculitis (diagnosis)", "Panniculitis, unspecified", "Inflammation of fat tissue", "Subcutaneous Adipose Tissue", "Subcutaneous adipose tissue", "Panniculitis, unspecified site", "Inflammation of adipose tissue", "subcutaneous adipose tissue inflammation", "inflammation of subcutaneous adipose tissue", "Panniculitis, unspecified, site unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "panniculitis", "shortest_name_length": 8}
{"curie": "MONDO:0003651", "names": ["Macrotrabecular Hepatoblastoma", "macrotrabecular hepatoblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macrotrabecular hepatoblastoma", "shortest_name_length": 30}
{"curie": "MONDO:0800126", "names": ["dystrophic pulmonary ossification"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dystrophic pulmonary ossification", "shortest_name_length": 33}
{"curie": "MONDO:0019087", "names": ["CC", "CCA", "Cholangiosarcoma", "cholangiosarcoma", "bile duct cancer", "Bile duct cancer", "cholangiocarcinoma", "Cholangiocarcinoma", "cholangiocarcinomas", "Cholangiocarcinomas", "Cholangiocarcinoma NOS", "Adult Cholangiocarcinoma", "Biliary cholangiocarcinoma", "Cholangiocellular carcinoma", "Cholangiocellular Carcinoma", "cholangiocellular carcinoma", "Cholangiocellular Carcinomas", "Carcinoma, Cholangiocellular", "CHOLANGIOCARCINOMA, MALIGNANT", "Carcinomas, Cholangiocellular", "cholangiocarcinoma, malignant", "Adult Primary Cholangiocarcinoma", "adult primary Cholangiocarcinoma", "adult primary cholangiocarcinoma", "Cholangiocar.- intra/extrahepatic", "Cholangiocarcinoma of biliary tract", "cholangiocarcinoma; unspecified site", "Adult Primary Cholangiocellular Carcinoma", "adult primary cholangiocellular carcinoma", "cholangiocellular carcinoma, adult primary", "Cholangiocarcinoma (morphologic abnormality)", "Cholangiocarcinoma of biliary tract (disorder)", "Cholangiocarcinoma of biliary tract (diagnosis)", "Intrahepatic Bile Duct Cancer (Cholangiocarcinoma)", "intrahepatic bile duct cancer (cholangiocarcinoma)", "malignant neoplasm of biliary tract cholangiocarcinoma", "cholangiocarcinoma, intrahepatic and extrahepatic bile ducts (adenocarcinoma)", "Cholangiocarcinoma, intrahepatic and extrahepatic bile ducts (adenocarcinoma)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholangiocarcinoma", "shortest_name_length": 2}
{"curie": "MONDO:0019134", "names": ["CNC", "neurocytoma", "Neurocytoma", "Neurocytomas", "neurocytomas", "Medullocytoma", "Neurolipocytoma", "central neurocytoma", "Central Neurocytoma", "Central neurocytoma", "Central Neurocytomas", "Neurocytoma, Central", "Neurocytomas, Central", "neurocytoma (diagnosis)", "Lipomatous medulloblastoma", "Central neurocytoma - histology", "Central Neurocytoma (WHO Grade 2)", "central neurocytoma (WHO grade II)", "Central Neurocytoma (WHO Grade II)", "Central neurocytoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central neurocytoma", "shortest_name_length": 3}
{"curie": "UMLS:C0153892", "names": ["Chloroma in Remission", "Chloroma (in remission)", "Chloroma (in Remission)", "myeloid sarcoma in remission", "Myeloid sarcoma in remission", "Myeloid Sarcoma in Remission", "Myeloid sarcoma, in remission", "Myeloid sarcoma (in remission)", "leukemia myeloid sarcoma in remission", "Myeloid sarcoma in remission (disorder)", "myeloid sarcoma in remission (diagnosis)", "Myeloid sarcoma, in remission, in remission"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myeloid sarcoma in remission", "shortest_name_length": 21}
{"curie": "UMLS:C0752144", "names": ["Brain Thromboses", "brain thrombosis", "Brain Thrombosis", "Thromboses, Brain", "thrombosis; brain", "Thrombosis, Brain", "brain; thrombosis", "brain; clot (blood)", "clot (blood); brain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brain Thrombosis", "shortest_name_length": 16}
{"curie": "UMLS:C4727359", "names": ["Recurrent Parotid Gland Acinic Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Parotid Gland Acinic Cell Carcinoma", "shortest_name_length": 45}
{"curie": "MONDO:0014578", "names": ["CMS17", "congenital myasthenic syndrome 17", "myasthenic syndrome, congenital, 17", "MYASTHENIC SYNDROME, CONGENITAL, 17", "LRP4 congenital myasthenic syndrome", "congenital myasthenic syndrome type 17", "myasthenic syndrome, congenital, type 17", "congenital myasthenic syndrome caused by mutation in LRP4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myasthenic syndrome 17", "shortest_name_length": 5}
{"curie": "UMLS:C2981419", "names": ["Stage IV Small Intestinal Gastrointestinal Stromal Tumor", "Stage IV Small Intestinal Gastrointestinal Stromal Tumor (GIST)", "Stage IV Small Intestinal Gastrointestinal Stromal Tumor AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Small Intestinal Gastrointestinal Stromal Tumor", "shortest_name_length": 56}
{"curie": "UMLS:C4683629", "names": ["St. Jude Stage I Childhood Non-Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "St. Jude Stage I Childhood Non-Hodgkin Lymphoma AJCC v8", "shortest_name_length": 55}
{"curie": "MONDO:0003670", "names": ["posteroinferior myocardial infarction", "Posteroinferior Myocardial Infarction by EKG Finding", "posteroinferior myocardial infarction by EKG finding", "Posteroinferior Myocardial Infarction by ECG Finding", "posteroinferior myocardial infarction by ECG finding"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "posteroinferior myocardial infarction", "shortest_name_length": 37}
{"curie": "MONDO:0016318", "names": ["pml", "PML", "JC Polyomavirus Encephalitis", "Encephalitis, JC Polyomavirus", "multifocal leukoencephalopathy", "Multifocal leukoencephalopathy", "Multifocal leucoencephalopathy", "JC Polyomavirus Encephalopathy", "Encephalopathy, JC Polyomavirus", "leukoencephalopathy; multifocal", "multifocal; leukoencephalopathy", "Encephalopathies, JC Polyomavirus", "Multifocal leukoencephalopathy NOS", "Multifocal leukoencephalopathy, NOS", "progressive multifocal leukoencephalitis", "Progressive multifocal leukoencephalitis", "progressive multifocal leukoencephalopathy", "Progressive multifocal leukoencephalopathy", "Progressive Multifocal Leukoencephalopathy", "Progressive multifocal leucoencephalopathy", "PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY", "leukoencephalopathy, progressive multifocal", "Leukoencephalopathy, Progressive Multifocal", "Multifocal Leukoencephalopathy, Progressive", "LEUKOENCEPHALOPATHY, PROGRESSIVE MULTIFOCAL", "Progressive Multifocal Leukoencephalopathies", "Multifocal Leukoencephalopathies, Progressive", "Leukoencephalopathies, Progressive Multifocal", "PML - Progressive multifocal leucoencephalopathy", "PML - Progressive multifocal leukoencephalopathy", "PMLE - Progressive multifocal leukoencephalopathy", "PMLE - Progressive multifocal leucoencephalopathy", "Progressive multifocal leukoencephalopathy (disorder)", "progressive multifocal leukoencephalopathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive multifocal leukoencephalopathy", "shortest_name_length": 3}
{"curie": "MONDO:0007660", "names": ["FGC", "Gigantiform cementoma", "cementoma; gigantiform", "gigantiform; cementoma", "Florid osseous dysplasia", "Jaffe-Campanacci syndrome", "familial ossifying fibroma", "Familial ossifying fibroma", "multiple ossifying fibroma", "Multiple ossifying fibroma", "Familial multiple cementoma", "Cementomas, familial multiple", "Cementomas, Familial Multiple", "CEMENTOMAS, FAMILIAL MULTIPLE", "Familial gigantiform cementoma", "CEMENTAL DYSPLASIA, PERIAPICAL", "Cemental Dysplasia, Periapical", "cemental dysplasia, periapical", "Gigantiform Cementoma, Familial", "intracortical fibrous dysplasia", "GIGANTIFORM cementoma, familial", "GIGANTIFORM CEMENTOMA, FAMILIAL", "hereditary ossifying fibroma (disease)", "Gigantiform cementoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial ossifying fibroma", "shortest_name_length": 3}
{"curie": "MONDO:0017552", "names": ["humero-ulnar fusion, unilateral", "humero-ulnar synostosis, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "humero-ulnar synostosis, unilateral", "shortest_name_length": 31}
{"curie": "UMLS:C0400968", "names": ["Liver transplant rejection", "liver transplant rejection", "liver transplant; rejection", "rejection; transplant, liver", "rejection of transplanted liver", "Liver transplant rejection (disorder)", "liver transplant rejection (diagnosis)", "rejection of transplanted liver (treatment)", "liver transplant post-transplant dysfunction rejection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liver transplant rejection", "shortest_name_length": 26}
{"curie": "UMLS:C0280240", "names": ["cancer of the renal pelvis and ureter, localized", "Upper Urinary Tract Localized Urothelial Carcinoma", "Localized Upper Urinary Tract Urothelial Carcinoma", "carcinoma of the renal pelvis and ureter, localized", "Localized Renal Pelvis and Ureter Urothelial Carcinoma", "Localized Urothelial Cancer of the Renal Pelvis and Ureter", "Renal pelvis and ureter transitional cell cancer localized", "Renal pelvis and ureteral cancer transitional cell localized", "Renal pelvis and ureteric cancer localized transitional cell", "Renal pelvis and ureteric cancer transitional cell localized", "Localized Urothelial Carcinoma of the Renal Pelvis and Ureter", "Localized Transitional Cell Cancer of Renal Pelvis and Ureter", "Localized Transitional Cell Carcinoma of Renal Pelvis and Ureter", "Localized Transitional Cell Cancer of the Renal Pelvis and Ureter", "Transitional cell cancer of the renal pelvis and ureter localized", "localized transitional cell cancer of the renal pelvis and ureter", "Transitional cell cancer of the renal pelvis and ureter localised", "transitional cell cancer of the renal pelvis and ureter, localized"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transitional cell cancer of the renal pelvis and ureter localized", "shortest_name_length": 48}
{"curie": "MONDO:0014073", "names": ["CMD1II", "dilated cardiomyopathy 1II", "CARDIOMYOPATHY, DILATED, 1II", "cardiomyopathy, dilated, 1II", "dilated cardiomyopathy type 1II", "cardiomyopathy, dilated, type 1II", "CRYAB familial isolated dilated cardiomyopathy", "familial isolated dilated cardiomyopathy caused by mutation in CRYAB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1II", "shortest_name_length": 6}
{"curie": "UMLS:C1333011", "names": ["Childhood Teratoma of Testis", "Childhood Testicular Teratoma", "Pediatric Testicular Teratoma", "Childhood Teratoma of the Testis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Testicular Teratoma", "shortest_name_length": 28}
{"curie": "UMLS:C0085997", "names": ["Developmental Delay Disorder", "Developmental Delay Disorders", "Child Development Disorders, Specific"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Child Development Disorders, Specific", "shortest_name_length": 28}
{"curie": "MONDO:0015546", "names": ["non-distal monosomy 10q", "non-distal deletion 10q", "non-telomeric monosomy 10q", "non-distal monosomy type 10q"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-distal monosomy 10q", "shortest_name_length": 23}
{"curie": "MONDO:0054806", "names": ["MCPH23", "MICROCEPHALY 23, PRIMARY, AUTOSOMAL RECESSIVE", "microcephaly 23, PRIMARY, autosomal recessive", "microcephaly 23, primary, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly 23, primary, autosomal recessive", "shortest_name_length": 6}
{"curie": "UMLS:C0338749", "names": ["continuous hallucinogen dependence", "Hallucinogen dependence, continuous", "Hallucinogen dependence, continuous use", "Hallucinogen Dependence, Continuous Use", "continuous hallucinogen dependence (diagnosis)", "Hallucinogen dependence, continuous (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hallucinogen dependence, continuous", "shortest_name_length": 34}
{"curie": "UMLS:C0751667", "names": ["Mild Canavan disease", "Type III Canavan Disease", "Juvenile Canavan disease", "Juvenile Canavan Disease", "Canavan Disease, Type III", "Canavan Disease, Juvenile"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Canavan Disease, Juvenile", "shortest_name_length": 20}
{"curie": "UMLS:C1262010", "names": ["Post lumbar puncture syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post lumbar puncture syndrome", "shortest_name_length": 29}
{"curie": "MONDO:0014199", "names": ["DEE17", "EIEE17", "GNAO1 encephalopathy", "early infantile epileptic encephalopathy 17", "early infantile epileptic encephalopathy-17", "developmental and epileptic encephalopathy 17", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 17", "epileptic encephalopathy, early infantile, 17", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 17", "developmental and epileptic encephalopathy, 17", "GNAO1 early infantile epileptic encephalopathy", "epileptic encephalopathy, early infantile, type 17", "early infantile epileptic encephalopathy caused by mutation in GNAO1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 17", "shortest_name_length": 5}
{"curie": "MONDO:0022993", "names": ["primary polydipsia", "Primary Polydipsia", "Dipsogenic Diabetes Insipidus", "Dipsogenic diabetes insipidus", "dipsogenic diabetes insipidus", "Dipsogenic diabetes insipidus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dipsogenic diabetes insipidus", "shortest_name_length": 18}
{"curie": "MONDO:0014064", "names": ["MC3DN3", "UQCRB mitochondrial complex III deficiency", "mitochondrial Complex 3 deficiency, nuclear type 3", "mitochondrial complex III deficiency nuclear type 3", "mitochondrial complex III deficiency, nuclear type 3", "MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 3", "mitochondrial complex III deficiency caused by mutation in UQCRB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex III deficiency nuclear type 3", "shortest_name_length": 6}
{"curie": "MONDO:0000673", "names": ["integrative agnosia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "integrative agnosia", "shortest_name_length": 19}
{"curie": "UMLS:C3854415", "names": ["Administration site swelling"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Administration site swelling", "shortest_name_length": 28}
{"curie": "MONDO:0006606", "names": ["scleredema", "Scleredema", "Scleroedema", "Scleredemas", "scleroedema", "scleredemas", "buschke scleredema", "Buschke scleredema", "Buschke Scleredema", "scleredema; Buschke", "Buschkes Scleredema", "Buschkes scleredema", "Buschke; scleredema", "Buschke's scleredema", "Scleredema Adultorum", "scleroderma; Buschke", "Buschke's Scleredema", "Buschke; scleroderma", "scleredema adultorum", "scleredema, Buschke's", "Scleredema of Buschke", "adultorum; scleredema", "Scleredema (disorder)", "scleredema; adultorum", "Scleredema, Buschke's", "Scleredema (diagnosis)", "scleredema Diabeticorum", "Scleredema Diabeticorum", "Scleredema diabeticorum", "Diabeticorum, Scleredema", "Diabeticorum, scleredema", "Scleroedema diabeticorum", "Scleredema Diabeticorums", "scleredema Diabeticorums", "skin disorder scleredema", "Diabeticorums, scleredema", "Diabeticorums, Scleredema", "disease; Buschke (etiology)", "Buschke; disease (etiology)", "Buschke Scleredema Adultorum", "Buschke scleredema adultorum", "Scleredema adultorum of Buschke", "Buschke Scleredema Diabeticorum", "scleredema adultorum of Buschke", "Scleredema Adultorum of Buschke", "Buschke scleredema Diabeticorum", "disease; Buschke (manifestation)", "Buschke; disease (manifestation)", "scleredema Diabeticorum of Buschke", "Scleredema Diabeticorum of Buschke"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scleredema adultorum", "shortest_name_length": 10}
{"curie": "MONDO:0012364", "names": ["CMD1Q", "dilated cardiomyopathy 1Q", "Cardiomyopathy, Dilated, 1q", "cardiomyopathy, dilated, 1Q", "CARDIOMYOPATHY, DILATED, 1Q", "dilated cardiomyopathy type 1Q", "CARDIOMYOPATHY, DILATED, 1Q (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1Q", "shortest_name_length": 5}
{"curie": "MONDO:0012451", "names": ["EOE1", "esophagitis, eosinophilic", "esophagitis, eosinophilic, 1", "ESOPHAGITIS, EOSINOPHILIC, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophagitis, eosinophilic, 1", "shortest_name_length": 4}
{"curie": "MONDO:0020467", "names": ["XX/XO", "mosaic monosomy X", "Mosaic Turner syndrome", "Mosaic monosomy type X", "Mosaic Turner syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mosaic monosomy X", "shortest_name_length": 5}
{"curie": "MONDO:0003600", "names": ["Skin Liposarcoma", "skin liposarcoma", "Liposarcoma of Skin", "liposarcoma of skin", "cutaneous liposarcoma", "Cutaneous Liposarcoma", "Liposarcoma of the Skin", "liposarcoma of the skin", "Liposarcoma of the skin", "zone of skin liposarcoma", "liposarcoma of zone of skin", "liposarcoma of skin (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous liposarcoma", "shortest_name_length": 16}
{"curie": "MONDO:0010484", "names": ["DFNX6", "X-linked deafness 6", "deafness, X-linked 6", "DEAFNESS, X-LINKED 6", "hearing loss, X-linked 6", "deafness, X-linked type 6", "COL4A6 X-linked nonsyndromic deafness", "deafness, X-linked 6, X-linked recessive", "X-linked nonsyndromic deafness caused by mutation in COL4A6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, X-linked 6", "shortest_name_length": 5}
{"curie": "MONDO:0019311", "names": ["Wooly hair nevus", "wooly hair nevus", "nevus wooly hair", "woolly hair nevus", "Woolly hair nevus", "woolly hair naevus", "NEVUS, WOOLLY HAIR", "Woolly hair naevus", "Wooly hair nevus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "woolly hair nevus", "shortest_name_length": 16}
{"curie": "UMLS:C4520920", "names": ["stage IV endometrial cancer", "stage IV cancer of the uterus", "Stage IV Endometrial Cancer AJCC v6", "Stage IV Uterine Corpus Cancer AJCC v6", "Stage IV Cancer of Uterine Corpus AJCC v6", "Stage IV Cancer of the Corpus Uteri AJCC v6", "Stage IV Cancer of the Uterine Corpus AJCC v6", "Stage IV Uterine (including Endometrial) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Uterine Corpus Cancer AJCC v6", "shortest_name_length": 27}
{"curie": "MONDO:0007237", "names": ["JHB", "Gigantomastia", "juvenile macromastia", "Adolescent macromastia", "Juvenile gigantomastia", "juvenile gigantomastia", "Gigantomastia, Juvenile", "GIGANTOMASTIA, JUVENILE", "gigantomastia, juvenile", "Pubertal breast hypertrophy", "virginal breast hypertrophy", "virginal mammary hypertrophy", "Juvenile mammary hypertrophy", "Diffuse hypertrophy of breast", "familial juvenile gigantomastia", "hypertrophy of the breast, juvenile", "HYPERTROPHY OF THE BREAST, JUVENILE", "Hypertrophy of the Breast, Juvenile", "Pubertal breast hypertrophy (disorder)", "familial juvenile hypertrophy of the breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial juvenile hypertrophy of the breast", "shortest_name_length": 3}
{"curie": "MONDO:0017987", "names": ["Syrinx", "Hydromyelia", "hydromyelia", "syringomyelia", "SYRINGOMYELIA", "Syringomyelia", "Syringomyelus", "Syringomyelias", "Myelosyringoses", "Myelosyringosis", "Hydrosyringomyelia", "hydrosyringomyelia", "Hydrosyringomyelias", "Spinal cord cavitation", "Syringomyelia (disorder)", "syringomyelia (diagnosis)", "Fluid-filled cyst in spinal cord", "Syringomyelia-anesthesia syndrome", "Syringomyelia-anaesthesia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syringomyelia", "shortest_name_length": 6}
{"curie": "UMLS:C4744374", "names": ["Sellar Chordoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sellar Chordoma", "shortest_name_length": 15}
{"curie": "MONDO:0004778", "names": ["epididymoorchitis", "EPIDIDYMOORCHITIS", "Epididymo-orchitis", "epididymo orchitis", "epididymo-orchitis", "orchitis epididymitis", "Orchitis/epididymitis", "epididymitis orchitis", "Epididymo-orchitis NOS", "Epididymo-orchitis, NOS", "Orchitis and epididymitis", "orchitis with epididymitis", "Orchitis and epididymitis (disorder)", "Inflammation of testis and epididymis", "Orchitis and epididymitis, unspecified", "orchitis with epididymitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epididymo-orchitis", "shortest_name_length": 17}
{"curie": "MONDO:0002860", "names": ["testis rhabdomyosarcoma", "Rhabdomyosarcoma of Testis", "rhabdomyosarcoma of testis", "Rhabdomyosarcoma of testis", "testicular rhabdomyosarcoma", "Testicular Rhabdomyosarcoma", "Rhabdomyosarcoma of the Testis", "rhabdomyosarcoma of the testis", "testis rhabdomyosarcoma (disease)", "rhabdomyosarcoma (disease) of testis", "testicular myosarcoma rhabdomyosarcoma", "rhabdomyosarcoma of testis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testis rhabdomyosarcoma", "shortest_name_length": 23}
{"curie": "UMLS:C5205717", "names": ["Sinonasal Adenocarcinoma, Salivary-Type", "Nasal Cavity and Paranasal Sinus Adenocarcinoma, Salivary-Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Adenocarcinoma, Salivary-Type", "shortest_name_length": 39}
{"curie": "UMLS:C4726601", "names": ["Undifferentiated Abdominal Pleomorphic Sarcoma", "Abdominal Undifferentiated Pleomorphic Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abdominal Undifferentiated Pleomorphic Sarcoma", "shortest_name_length": 46}
{"curie": "MONDO:0023571", "names": ["Kozlowski Rafinski Klicharska syndrome", "metaphyseal and epiphyseal dysplasia with unusual facies and cataract", "Metaphyseal and epiphyseal dysplasia with unusual facies and cataract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kozlowski Rafinski Klicharska syndrome", "shortest_name_length": 38}
{"curie": "UMLS:C1369008", "names": ["Hybrid Resistance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hybrid Resistance", "shortest_name_length": 17}
{"curie": "MONDO:0001773", "names": ["Vaccination Encephalitis", "Postvaccinal Encephalitis", "Postvaccinal encephalitis", "Encephalitis, Vaccination", "Post-Vaccinal Encephalitis", "Encephalitis, Postvaccinal", "post-vaccinal encephalitis", "Post Vaccinal Encephalitis", "Encephalitis, Post-Vaccinal", "Encephalitis, Post Vaccinal", "Post-Vaccinal Encephalitides", "postvaccinal encephalomyelitis", "Postvaccinal encephalomyelitis", "POSTVACCINAL ENCEPHALOMYELITIS", "Post Vaccinal Encephalomyelitis", "Post-Vaccinal Encephalomyelitis", "Encephalomyelitis, Post-Vaccinal", "Post-Vaccinal Encephalomyelitides", "Post-immunization encephalomyelitis", "Post-immunisation encephalomyelitis", "Encephalomyelitis, post immunization", "Postvaccinal encephalomyelitis (disorder)", "Encephalitis following immunization procedures", "encephalitis following immunization procedures", "Encephalitis following immunisation procedures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "post-vaccinal encephalitis", "shortest_name_length": 24}
{"curie": "MONDO:0011839", "names": ["NFRCD", "RLBP1 cone-rod dystrophy", "NEWFOUNDLAND ROD-CONE DYSTROPHY", "Newfoundland Rod-Cone Dystrophy", "Newfoundland cone-rod dystrophy", "Newfoundland ROD-cone dystrophy", "cone-rod dystrophy caused by mutation in RLBP1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Newfoundland cone-rod dystrophy", "shortest_name_length": 5}
{"curie": "UMLS:C4763429", "names": ["Recurrent Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Neuroendocrine Neoplasm", "shortest_name_length": 33}
{"curie": "UMLS:C5442191", "names": ["CCUS", "Clonal Cytopenia of Undetermined Significance", "CCUS Clonal Cytopenia of Undetermined Significance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clonal Cytopenia of Undetermined Significance", "shortest_name_length": 4}
{"curie": "UMLS:C1378108", "names": ["Pharyngeal Cancer Stage II", "Stage II Pharynx Carcinoma", "Stage II Pharyngeal Cancer", "Stage II Pharyngeal Carcinoma", "Stage II Carcinoma of Pharynx", "Stage II Carcinoma of the Pharynx", "Stage II Pharyngeal Throat Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Pharynx Carcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0003404", "names": ["yolk Sac tumor", "Yolk Sac Tumor", "Adult Yolk Sac Tumor", "adult yolk sac tumor", "adult yolk Sac tumor", "adult yolk Sac neoplasm", "adult Yolk Sac neoplasm", "Adult Yolk Sac Neoplasm", "yolk sac tumor of adults", "adult endodermal sinus tumor", "Adult Endodermal Sinus Tumor", "adult endodermal sinus neoplasm", "Adult Endodermal Sinus Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult yolk sac tumor", "shortest_name_length": 14}
{"curie": "MONDO:0010281", "names": ["GSD IIb", "Danon disease", "Danon Disease", "DANON DISEASE", "Antopol Disease", "Antopol disease", "ANTOPOL DISEASE", "ANTOPOL disease", "GSD2B, FORMERLY", "Disease, Antopol", "GSD2B (formerly)", "GSD IIb, FORMERLY", "GSD IIb, formerly", "Glycogenosis Type 2b", "pseudoglycogenosis 2", "Pseudoglycogenosis 2", "Pseudoglycogenosis 2s", "PSEUDOGLYCOGENOSIS II", "Pseudoglycogenosis II", "pseudoglycogenosis II", "Pseudoglycogenosis IIs", "Danon disease (disorder)", "Danon disease (diagnosis)", "glycogen storage disease IIb", "GSD due to LAMP-2 deficiency", "GLYCOGEN STORAGE DISEASE IIb", "Glycogen Storage Disease IIb", "glycogen storage cardiomyopathy", "Glycogen Storage Cardiomyopathy", "Glycogen Storage Disease Type 2B", "Glycogen Storage Disease Type 2b", "Danon disease, X-linked dominant", "Cardiomyopathy, Glycogen Storage", "Glycogen Storage Disease Type IIb", "glycogen storage disease type IIb", "Glycogen Storage Cardiomyopathies", "Cardiomyopathies, Glycogen Storage", "Glycogenosis due to LAMP-2 deficiency", "glycogenosis due to LAMP-2 deficiency", "LAMP2 lysosomal glycogen storage disease", "glycogen storage disease type 2b (formerly)", "Glycogen Storage Disease Limited to the Heart", "X Linked Vacuolar Cardiomyopathy and Myopathy", "X-linked vacuolar cardiomyopathy and myopathy", "glycogen storage disease limited to the heart", "vacuolar cardiomyopathy and myopathy X-linked", "X-Linked Vacuolar Cardiomyopathy and Myopathy", "Vacuolar Cardiomyopathy and Myopathy, X linked", "Vacuolar Cardiomyopathy and Myopathy, X-linked", "vacuolar cardiomyopathy and myopathy, X-linked", "VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED", "glycogen storage disease due to LAMP-2 deficiency", "Glycogen storage disease due to LAMP-2 deficiency", "Lysosomal Glycogen Storage Disease with Normal Acid Maltase", "lysosomal glycogen storage disease caused by mutation in LAMP2", "lysosomal glycogen storage disease without acid maltase deficiency", "Lysosomal Glycogen Storage Disease without Acid Maltase Deficiency", "lysosomal glycogen storage disease with normal acid maltase activity", "Lysosomal glycogen storage disease with normal acid maltase activity", "LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY, FORMERLY", "lysosomal glycogen storage disease without acid maltase deficiency, formerly", "lysosomal glycogen storage disease without acid maltase deficiency (formerly)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Danon disease", "shortest_name_length": 7}
{"curie": "MONDO:0003652", "names": ["Uric acid stones", "Urate urolithiasis", "uric acid urolithiasis", "Uric acid urolithiasis", "Uric Acid Urolithiasis", "Acute urate nephropathy", "acute urate nephropathy", "Uric acid nephrolithiasis", "Uric Acid Nephrolithiasis", "uric acid nephrolithiasis", "Uric acid urolithiasis (disorder)", "Acute urate nephropathy (disorder)", "acute urate nephropathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute urate nephropathy", "shortest_name_length": 16}
{"curie": "MONDO:0000339", "names": ["spinal polio"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal polio", "shortest_name_length": 12}
{"curie": "UMLS:C0267033", "names": ["Lip sore", "lip ulcer", "Sores lip", "ULCER LIP", "LIP ULCER", "Lip ulcer", "Ulcer lip", "lip sores", "lip; ulcer", "ulcer; lip", "lip ulcers", "lips ulcers", "Ulcer of lip", "sores on lips", "Lip ulceration", "LIP ULCERATION", "sores on the lips", "Lip ulcer (disorder)", "sores on lips (symptom)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lip ulcer (disorder)", "shortest_name_length": 8}
{"curie": "MONDO:0009960", "names": ["IBD1", "Crohn disease", "regional enteritis", "ulcerative colitis", "inflammatory bowel disease 1", "pediatric ulcerative colitis", "ulcerative colitis, pediatric", "NOD2 inflammatory bowel disease", "inflammatory bowel disease type 1", "crohn disease-associated growth failure", "inflammatory bowel disease 1, Crohn disease", "inflammatory bowel disease (Crohn disease) 1", "inflammatory bowel disease caused by mutation in NOD2", "Crohn disease-associated Growth failure, susceptibility to", "CROHN DISEASE-ASSOCIATED GROWTH FAILURE, SUSCEPTIBILITY TO", "CROHN DISEASE-ASSOCIATED GROWTH FAILURE, SUSCEPTIBILITY TO (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory bowel disease 1", "shortest_name_length": 4}
{"curie": "UMLS:C2981627", "names": ["Stage IVA Intrahepatic Cholangiocarcinoma", "Stage IVA Intrahepatic Cholangiocarcinoma AJCC v7", "Stage IVA Intrahepatic Bile Duct Cancer (Cholangiocarcinoma)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Intrahepatic Cholangiocarcinoma AJCC v7", "shortest_name_length": 41}
{"curie": "UMLS:C1096035", "names": ["Infusion site pain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infusion site pain", "shortest_name_length": 18}
{"curie": "MONDO:0009511", "names": ["JDSCD", "Larsen Syndrome, Recessive", "Larsen syndrome, recessive type", "Larsen-like syndrome B3GAT3 type", "Larsen-like syndrome, B3GAT3 type", "Autosomal Recessive Larsen Syndrome", "Autosomal recessive Larsen syndrome", "Larsen syndrome, autosomal recessive", "LARSEN SYNDROME, AUTOSOMAL RECESSIVE, FORMERLY", "Larsen syndrome, autosomal recessive, formerly", "multiple JOINT dislocations, short stature, craniofacial dysmorphism, and congenital heart defects", "multiple joint dislocations-short stature-craniofacial dysmorphism-congenital heart defects syndrome", "MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH CONGENITAL HEART DEFECTS", "multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects", "multiple Joint dislocations, short stature, and craniofacial Dysmorphism with or without congenital heart defects", "MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS", "multiple JOINT dislocations, short stature, and craniofacial dysmorphism with or without congenital heart defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Larsen-like syndrome, B3GAT3 type", "shortest_name_length": 5}
{"curie": "MONDO:0043069", "names": ["Zerres Rietschel Majewski syndrome", "postnatal short stature, microcephaly, severe syndactyly of hands and feet, dysmorphic face, and mental retardation", "postnatal short stature, microcephaly, severe syndactyly of hands and feet, dysmorphic face, and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Zerres Rietschel Majewski syndrome", "shortest_name_length": 34}
{"curie": "MONDO:0043988", "names": ["Zoster sine herpete", "Zoster Sine Herpete", "zoster sine herpete", "Zoster Sine Eruptione", "Zoster sine Eruptione", "Zoster sine herpete (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "zoster sine herpete", "shortest_name_length": 19}
{"curie": "MONDO:0018550", "names": ["SPOAN and SPOAN-related disorder", "spastic paraplegia-optic atrophy-neuropathy and spastic paraplegia-optic atrophy-neuropathy-related disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic paraplegia-optic atrophy-neuropathy and spastic paraplegia-optic atrophy-neuropathy-related disorder", "shortest_name_length": 32}
{"curie": "UMLS:C0267446", "names": ["acute gastroenteritis", "Acute gastroenteritis", "gastroenteritis acute", "Acute gastroenteritis, NOS", "Acute gastroenteritis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute gastroenteritis", "shortest_name_length": 21}
{"curie": "UMLS:C0750992", "names": ["Lethal Catatonia", "lethal catatonia", "Lethal catatonia", "Lethal Catatonias", "Catatonia, Lethal", "Catatonias, Lethal", "Malignant catatonia", "Malignant Catatonia", "Malignant Catatonias", "Catatonia, Malignant", "Catatonias, Malignant", "Lethal catatonia (disorder)", "lethal catatonia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Catatonia, Malignant", "shortest_name_length": 16}
{"curie": "UMLS:C5418823", "names": ["Unresectable Desmoplastic Small Round Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Desmoplastic Small Round Cell Tumor", "shortest_name_length": 48}
{"curie": "UMLS:C5556742", "names": ["Urethral Adenocarcinoma of Skene Gland Origin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urethral Adenocarcinoma of Skene Gland Origin", "shortest_name_length": 45}
{"curie": "MONDO:0011289", "names": ["Eyelid opening apraxia", "apraxia of eyelid opening", "Apraxia of eyelid opening", "APRAXIA OF EYELID OPENING"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "apraxia of eyelid opening", "shortest_name_length": 22}
{"curie": "MONDO:0100337", "names": ["SEC61A1 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SEC61A1 deficiency", "shortest_name_length": 18}
{"curie": "MONDO:0014027", "names": ["HYPT11", "hypt11", "Hypt11", "HYPOTRICHOSIS 11", "hypotrichosis 11", "SNRPE hypotrichosis", "hypotrichosis type 11", "hypotrichosis caused by mutation in SNRPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotrichosis 11", "shortest_name_length": 6}
{"curie": "MONDO:0005354", "names": ["Chronic hepatitis C", "c chronic hepatitis", "chronic hepatitis c", "chronic hepatitis C", "chronic Hepatitis C", "hepatitis c chronic", "Chronic Hepatitis C", "Hepatitis C, Chronic", "hepatitis C, chronic", "Chronic viral hepatitis C", "chronic hepatitis, C virus", "Chronic hepatitis C (disorder)", "Chronic type C viral hepatitis", "hepatitis C infection, chronic", "chronic hepatitis C (diagnosis)", "hepatitis; virus, chronic, type C", "chronic hepatitis C virus infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic hepatitis C virus infection", "shortest_name_length": 19}
{"curie": "UMLS:C1336178", "names": ["Breast Cancer Stage IIB", "Stage IIB Breast Cancer", "stage IIB breast cancer", "stage IIB breast carcinoma", "Breast Carcinoma Stage IIB", "Stage IIB Breast Carcinoma", "breast carcinoma stage IIB", "Stage IIB Breast Cancer AJCC v6", "Stage IIB Breast Cancer AJCC v7", "stage IIB breast cancer AJCC v7", "Stage IIB Breast Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Breast Carcinoma", "shortest_name_length": 23}
{"curie": "UMLS:C4054375", "names": ["Malaria Associated Nephrotic Syndrome", "Nephrotic Syndrome - Malaria Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - Malaria Associated", "shortest_name_length": 37}
{"curie": "MONDO:0022770", "names": ["circumscribed cutaneous aplasia of the vertex"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "circumscribed cutaneous aplasia of the vertex", "shortest_name_length": 45}
{"curie": "MONDO:0020630", "names": ["DEE91", "IECEE1", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 91", "developmental and epileptic encephalopathy 91", "infantile or early childhood epileptic encephalopathy 1", "epileptic encephalopathy, infantile or early childhood, 1", "EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epileptic encephalopathy, infantile or early childhood, 1", "shortest_name_length": 5}
{"curie": "UMLS:C4324523", "names": ["Intercepted product storage error"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intercepted product storage error", "shortest_name_length": 33}
{"curie": "MONDO:0003837", "names": ["TSHoma", "TSH-oma", "Thyrotroph adenoma", "Thyrotrope Adenoma", "thyrotroph adenoma", "TSH-producing Adenoma", "Thyrotroph PitNET/Adenoma", "TSH producing pituitary tumor", "TSH secreting pituitary tumor", "TSH producing pituitary tumour", "TSH Secreting Pituitary Adenoma", "TSH Producing Pituitary Adenoma", "TSH secreting pituitary neoplasm", "TSH secreting tumor of pituitary", "TSH producing pituitary neoplasm", "TSH Secreting tumor of Pituitary", "TSH producing tumor of pituitary", "TSH Secreting tumour of Pituitary", "TSH Producing Adenoma of Pituitary", "TSH Secreting Adenoma of Pituitary", "TSH-Producing Pituitary Gland Tumor", "TSH secreting neoplasm of pituitary", "TSH producing neoplasm of pituitary", "TSH producing pituitary gland tumor", "TSH-producing pituitary gland tumor", "TSH secreting pituitary gland tumor", "TSH secreting tumor of the pituitary", "TSH producing tumor of the pituitary", "TSH-Producing Pituitary Gland Adenoma", "TSH Producing Pituitary Gland Adenoma", "TSH Secreting Pituitary Gland Adenoma", "TSH producing tumor of pituitary gland", "TSH secreting adenoma of the pituitary", "TSH Secreting adenoma of the Pituitary", "TSH-producing pituitary gland neoplasm", "TSH producing pituitary gland neoplasm", "TSH Secreting Adenoma of the Pituitary", "TSH secreting tumor of pituitary gland", "TSH Producing Adenoma of the Pituitary", "TSH secreting pituitary gland neoplasm", "TSH producing neoplasm of the pituitary", "thyrotropin-secreting pituitary adenoma", "TSH secreting neoplasm of the pituitary", "TSH Producing Adenoma of Pituitary Gland", "TSH Secreting Adenoma of Pituitary Gland", "TSH producing neoplasm of pituitary gland", "TSH secreting neoplasm of pituitary gland", "Thyrotroph Pituitary Neuroendocrine Tumor", "TSH producing tumor of the pituitary gland", "TSH secreting tumor of the pituitary gland", "TSH Secreting Adenoma of the Pituitary Gland", "TSH Producing Adenoma of the Pituitary Gland", "thyroid stimulating hormone producing tumour", "TSH secreting neoplasm of the pituitary gland", "Thyroid Stimulating Hormone-Producing Adenoma", "TSH producing neoplasm of the pituitary gland", "Thyrotropin Producing Pituitary Gland Adenoma", "thyrotropin producing pituitary gland neoplasm", "Thyrotroph Pituitary Neuroendocrine Tumor/Adenoma", "Thyroid stimulating hormone-producing pituitary tumor", "thyroid stimulating hormone secreting pituitary tumor", "thyroid stimulating hormone producing pituitary tumor", "Thyroid stimulating hormone-producing pituitary tumour", "Thyroid Stimulating Hormone Producing Pituitary Adenoma", "Thyroid Stimulating Hormone Secreting Pituitary Adenoma", "thyroid stimulating hormone producing tumor of pituitary", "thyroid stimulating hormone producing pituitary neoplasm", "thyroid stimulating hormone secreting pituitary neoplasm", "thyroid stimulating hormone secreting tumor of pituitary", "Thyroid Stimulating Hormone Producing Adenoma of Pituitary", "Thyroid Stimulating Hormone Secreting Adenoma of Pituitary", "thyroid stimulating hormone secreting neoplasm of pituitary", "thyroid stimulating hormone secreting pituitary gland tumor", "thyroid stimulating hormone producing pituitary gland tumor", "thyroid stimulating hormone producing neoplasm of pituitary", "thyroid stimulating hormone secreting tumor of the pituitary", "thyroid stimulating hormone producing tumor of the pituitary", "Thyroid Stimulating Hormone Secreting Pituitary Gland Adenoma", "Thyroid Stimulating Hormone Producing Pituitary Gland Adenoma", "thyroid stimulating hormone producing pituitary gland neoplasm", "thyroid stimulating hormone secreting pituitary gland neoplasm", "thyroid stimulating hormone producing tumor of pituitary gland", "Thyroid Stimulating Hormone Secreting Adenoma of the Pituitary", "thyroid stimulating hormone secreting tumor of pituitary gland", "Thyroid Stimulating Hormone Producing Adenoma of the Pituitary", "thyroid stimulating hormone secreting neoplasm of the pituitary", "thyroid stimulating hormone producing neoplasm of the pituitary", "Thyroid Stimulating Hormone Producing Adenoma of Pituitary Gland", "Thyroid Stimulating Hormone Secreting Adenoma of Pituitary Gland", "thyroid stimulating hormone secreting neoplasm of pituitary gland", "thyroid stimulating hormone producing neoplasm of pituitary gland", "thyroid stimulating hormone producing tumor of the pituitary gland", "thyroid stimulating hormone secreting tumor of the pituitary gland", "Thyroid Stimulating Hormone Secreting Adenoma of the Pituitary Gland", "Thyroid Stimulating Hormone Producing Adenoma of the Pituitary Gland", "thyroid stimulating hormone secreting neoplasm of the pituitary gland", "thyroid stimulating hormone producing neoplasm of the pituitary gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "TSH producing pituitary tumor", "shortest_name_length": 6}
{"curie": "UMLS:C0877265", "names": ["Trichophyton infection", "Trichophyton infections", "Trichophyton infection NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Trichophyton infection", "shortest_name_length": 22}
{"curie": "UMLS:C2828101", "names": ["Stage IIIC Vulvar Cancer", "stage IIIC vulvar cancer", "stage IIIC vulvar carcinoma", "Stage IIIC Vulvar Carcinoma", "Stage IIIC Vulvar Cancer AJCC v7", "stage IIIC vulvar cancer AJCC v7", "stage IIIC vulvar carcinoma AJCC v7", "Stage IIIC Vulvar Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Vulvar Cancer AJCC v7", "shortest_name_length": 24}
{"curie": "UMLS:C2226910", "names": ["anal wound", "anal injury", "Anal Injury", "Anal injury", "anus; wound", "wound; anus", "anus; injury", "injury; anus", "wound of anus", "Injury of anus", "injuries to the anus", "Injury of anus (disorder)", "pelvic cavity injury anus", "Injury of anus (diagnosis)", "anal injury (physical finding)", "wound of anus (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of anus", "shortest_name_length": 10}
{"curie": "UMLS:C5420164", "names": ["Nasopharyngeal PitNET/Adenoma", "Nasopharyngeal Pituitary Gland Adenoma", "Nasopharyngeal Pituitary Neuroendocrine Tumor", "Nasopharyngeal Pituitary Neuroendocrine Tumor/Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasopharyngeal Pituitary Neuroendocrine Tumor", "shortest_name_length": 29}
{"curie": "UMLS:C0333898", "names": ["Moderate koilocytotic atypia", "Moderate Koilocytotic Atypia", "Moderate koilocytotic atypia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Moderate koilocytotic atypia", "shortest_name_length": 28}
{"curie": "MONDO:0033370", "names": ["DEE61", "EIEE61", "early infantile epileptic encephalopathy 61", "epileptic encephalopathy, early infantile, 61", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 61", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 61", "developmental and epileptic encephalopathy 61", "developmental and epileptic encephalopathy, 61"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 61", "shortest_name_length": 5}
{"curie": "MONDO:0019655", "names": ["sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis", "sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental glomerulosclerosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis", "shortest_name_length": 88}
{"curie": "MONDO:0007715", "names": ["hemolytic poikilocytic anemia due to reduced ankyrin binding sites", "HEMOLYTIC POIKILOCYTIC ANEMIA DUE TO REDUCED ANKYRIN BINDING SITES", "Hemolytic Poikilocytic Anemia due to Reduced Ankyrin Binding Sites"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemolytic poikilocytic anemia due to reduced ankyrin binding sites", "shortest_name_length": 66}
{"curie": "UMLS:C0018245", "names": ["Groenouw Dystrophies", "Groenouws Dystrophies", "Groenouw's Dystrophies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Groenouw's Dystrophies", "shortest_name_length": 20}
{"curie": "UMLS:C1518022", "names": ["Ovarian Endometrioid Stromal Sarcoma", "Endometrioid Stromal Sarcoma of the Ovary", "Ovarian Low Grade Endometrioid Stromal Sarcoma", "Low Grade Endometrioid Stromal Sarcoma of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Low Grade Endometrioid Stromal Sarcoma", "shortest_name_length": 36}
{"curie": "MONDO:0004203", "names": ["female urethra cancer", "female urethral cancer", "cancer of female urethra", "malignant female urethra neoplasm", "female urethral malignant neoplasm", "Female Urethral Malignant Neoplasm", "malignant neoplasm of female urethra"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "female urethral cancer", "shortest_name_length": 21}
{"curie": "MONDO:0044725", "names": ["IMD55", "IMMUNODEFICIENCY 55", "immunodeficiency 55", "CID due to GINS1 deficiency", "Combined immunodeficiency due to GINS1 deficiency", "combined immunodeficiency due to GINS1 deficiency", "Combined immunodeficiency due to GINS complex subunit 1 deficiency", "Combined immunodeficiency due to GINS1 (GINS complex subunit 1) deficiency", "Combined immunodeficiency due to GINS complex subunit 1 deficiency (disorder)", "Combined immunodeficiency with intrauterine growth retardation-NK cell deficiency-neutropenia", "combined immunodeficiency with intrauterine growth retardation-NK cell deficiency-neutropenia", "Combined immunodeficiency with intrauterine growth retardation-natural killer cell deficiency-neutropenia", "combined immunodeficiency with intrauterine growth retardation-natural killer cell deficiency-neutropenia", "Combined immunodeficiency with intrauterine growth retardation, NK (natural killer) cell deficiency, neutropenia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined immunodeficiency due to GINS1 deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0007867", "names": ["NDNC2", "spoon nail", "SPOON NAILS", "Spoon nails", "spoon nails", "nails spoon", "koilonychia", "Koilonychia", "KOILONYCHIA", "Concave nail", "SPOONED NAILS", "Concave nails", "spooned nails", "nail spooning", "NAILBED SPOONING", "Spoon-shaped nails", "familial koilonychia", "Familial koilonychia", "Hereditary koilonychia", "Congenital Koilonychia", "congenital koilonychia", "hereditary koilonychia", "spoon nail; congenital", "Congenital koilonychia", "Koilonychia (disorder)", "congenital; spoon nail", "congenital; koilonychia", "Koilonychia, Hereditary", "KOILONYCHIA, HEREDITARY", "Koilonychia, hereditary", "koilonychia; congenital", "Koilonychia with leukonychia", "KOILONYCHIA WITH LEUKONYCHIA", "Congenital koilonychia (disorder)", "congenital koilonychia (diagnosis)", "nonsyndromic congenital nail disorder 2", "nail disorder, nonsyndromic congenital, 2", "NAIL DISORDER, NONSYNDROMIC CONGENITAL, 2", "nonsyndromic congenital nail disorder type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nonsyndromic congenital nail disorder 2", "shortest_name_length": 5}
{"curie": "MONDO:0021317", "names": ["cerebellum cancer", "cerebellar cancer", "Cerebellar Cancer", "Cerebellar Cancers", "Cancer, Cerebellar", "Cancer of cerebellum", "cancer of cerebellum", "Cancer of Cerebellum", "cancer of the cerebellum", "Cancer of the Cerebellum", "Malignant Cerebellar Tumor", "malignant cerebellar tumor", "Cerebellar Tumor, Malignant", "cerebellar tumor, malignant", "malignant cerebellar neoplasm", "malignant tumor of cerebellum", "Malignant Cerebellar Neoplasm", "Malignant Tumor of Cerebellum", "malignant cerebellum neoplasm", "Cerebellar Neoplasm, Malignant", "Neoplasm, Malignant Cerebellar", "Malignant Cerebellar Neoplasms", "malignant cerebellar neoplasms", "cerebellar neoplasm, malignant", "Cerebellar Neoplasms, Malignant", "Malignant neoplasm of cerebellum", "Malignant Neoplasm of Cerebellum", "malignant neoplasm of cerebellum", "Neoplasms, Cerebellar, Malignant", "malignant tumor of the cerebellum", "Malignant Tumor of the Cerebellum", "Malignant neoplasm of cerebellum nos", "Malignant Neoplasm of the Cerebellum", "Malignant neoplasm of cerebellum NOS", "malignant neoplasm of the cerebellum", "Malignant neoplasm of cerebellum (disorder)", "malignant neoplasm of cerebellum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cancer of cerebellum", "shortest_name_length": 17}
{"curie": "UMLS:C5205724", "names": ["Oligometastatic tumor", "Oligometastatic tumour", "Oligometastatic disease", "Oligometastatic Disease", "Oligometastatic malignant neoplasm", "Oligometastatic malignant neoplastic disease", "Oligometastatic secondary malignant neoplasm", "Oligometastatic malignant neoplasm (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oligometastatic malignant neoplasm", "shortest_name_length": 21}
{"curie": "UMLS:C0854787", "names": ["Non-Resectable Small Bowel Carcinoma", "Unresectable Small Intestinal Cancer", "Unresectable Small Intestine Carcinoma", "Unresectable Small Intestinal Carcinoma", "Non-Resectable Carcinoma of Small Bowel", "Non-Resectable Small Intestine Carcinoma", "Small intestine carcinoma non-resectable", "Small Intestine Carcinoma, Non-Resectable", "Non-Resectable Carcinoma of the Small Bowel", "Non-Resectable Carcinoma of Small Intestine", "Non-Resectable Carcinoma of the Small Intestine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small intestine carcinoma non-resectable", "shortest_name_length": 36}
{"curie": "UMLS:C0279585", "names": ["non T, non B pediatric ALL", "non T, non B childhood ALL", "non-T, non-B childhood ALL", "non-T, non-B pediatric ALL", "pediatric ALL, non T, non B", "pediatric ALL, non-T, non-B", "non-T, non-B ALL, childhood", "childhood ALL, non-T, non-B", "childhood ALL, non T, non B", "non-T, non-B ALL, pediatric", "non T, non B ALL, pediatric", "non T, non B ALL, childhood", "ALL, childhood, non T, non B", "ALL, non-T, non-B, pediatric", "ALL, pediatric, non-T, non-B", "ALL, non-T, non-B, childhood", "ALL, non T, non B, childhood", "ALL, pediatric, non T, non B", "ALL, non T, non B, pediatric", "ALL, childhood, non-T, non-B", "leukemia, pediatric ALL non-T, non-B", "leukemia, childhood ALL non-T, non-B", "Non-T Non-B Acute Lymphoblastic Leukemia", "non-T, non-B pediatric acute lymphocytic leukemia", "non-T, non-B childhood acute lymphocytic leukemia", "non-B, non-T childhood acute lymphocytic leukemia", "non B, non T childhood acute lymphocytic leukemia", "non T, non B childhood acute lymphocytic leukemia", "non B, non T pediatric acute lymphocytic leukemia", "Childhood Non-T Non-B Acute Lymphoblastic Leukemia", "acute lymphocytic leukemia, childhood non-T, non-B", "non-T, non-B acute lymphocytic leukemia, childhood", "childhood acute lymphocytic leukemia, non-T, non-B", "leukemia, childhood acute lymphocytic non-T, non-B", "non-T, non-B childhood acute lymphoblastic leukemia", "leukemia, pediatric acute lymphocytic, non-T, non-B", "pediatric acute lymhoblastic leukemia, non-T, non-B", "childhood acute lymphoblastic leukemia, non-T, non-B", "acute lymphoblastic leukemia, childhood non-T, non-B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Non-T Non-B Acute Lymphoblastic Leukemia", "shortest_name_length": 26}
{"curie": "MONDO:0013359", "names": ["FH3", "FH 3", "HALD3", "FH III", "FH-III", "familial hyperaldosteronism type 3", "Familial hyperaldosteronism type 3", "Familial Hyperaldosteronism Type 3", "hyperaldosteronism, familial, type 3", "familial hyperaldosteronism type III", "Familial hyperaldosteronism type III", "HYPERALDOSTERONISM, FAMILIAL, TYPE III", "hyperaldosteronism, familial, type III", "Familial hyperaldosteronism type 3 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial hyperaldosteronism type III", "shortest_name_length": 3}
{"curie": "MONDO:0005757", "names": ["Eumycetoma", "eumycetoma", "Madura foot", "maduromycosis", "Maduromycosis", "Fungal mycetoma", "Mycotic mycetoma", "MYCOTIC MYCETOMA", "Mycetoma mycotic", "mycotic mycetoma", "mycotic; mycetoma", "Mycotic mycetomas", "mycetoma; mycotic", "eumycotic mycetoma", "Eumycotic mycetoma", "mycetoma; eumycotic", "eumycotic; mycetoma", "Madura foot, mycotic", "Mycotic maduromycosis", "Madura foot - mycotic", "Maduromycosis, mycotic", "infection; mycetoma, mycotic", "mycetoma; infection, mycotic", "Eumycotic mycetoma (disorder)", "eumycotic mycetoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eumycotic mycetoma", "shortest_name_length": 10}
{"curie": "MONDO:0018215", "names": ["PCD", "PNS", "paraneoplastic neurologic syndrome", "paraneoplastic cerebellar degeneration", "nervous system paraneoplastic syndrome", "paraneoplastic syndrome of nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paraneoplastic neurologic syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0009933", "names": ["CPL", "lymphangiomatosis pulmonary", "pulmonary lymphangiomatosis", "Pulmonary lymphangiomatosis", "LYMPHANGIOMATOSIS, PULMONARY", "lymphangiomatosis, pulmonary", "Lymphangiomatosis, pulmonary", "pulmonary cystic lymphangiectasis", "Pulmonary cystic lymphangiectasis", "PULMONARY CYSTIC LYMPHANGIECTASIS", "Lymphangiectasia pulmonary congenital", "congenital pulmonary lymphangiectasis", "Congenital pulmonary lymphangiectasis", "congenital pulmonary lymphangiectasia", "lymphangiectasia pulmonary congenital", "Congenital Pulmonary Lymphangiectasis", "Congenital Pulmonary Lymphangiectasia", "Congenital pulmonary lymphangiectasia", "Pulmonary lymphangiectasia, congenital", "Lymphangiectasia, pulmonary, congenital", "lymphangiectasia, pulmonary, congenital", "LYMPHANGIECTASIA, PULMONARY, CONGENITAL", "Congenital pulmonary lymphangiectasis (disorder)", "Congenital pulmonary lymphangiectasis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital pulmonary lymphangiectasia", "shortest_name_length": 3}
{"curie": "MONDO:0005029", "names": ["ET", "primary thrombocytosis", "Primary thrombocytosis", "primary Thrombocytosis", "Primary Thrombocytoses", "Primary Thrombocytosis", "primary thrombocythemia", "Primary thrombocythemia", "Thrombocytoses, Primary", "Thrombocytosis, Primary", "familial thrombocytosis", "Primary Thrombocythemia", "essential thrombocytemia", "Essential Thrombocytosis", "Primary Thrombocythemias", "Primary thrombocythaemia", "thrombocytosis essential", "THROMBOCYTOSIS ESSENTIAL", "Thrombocythemia, Primary", "essential thrombocytosis", "Essential thrombocytosis", "Thrombocytosis;essential", "Essential Thrombocytemia", "Essential Thrombocythemia", "essential thrombocythemia", "Thrombocythemias, Primary", "ESSENTIAL THROMBOCYTHEMIA", "Idiopathic thrombocytosis", "idiopathic thrombocytosis", "Essential thrombocythemia", "thrombocytosis; essential", "thrombocythemia essential", "essential thrombocythaemia", "Idiopathic Thrombocythemia", "Thrombocythemia, Essential", "thrombocythemia, essential", "THROMBOCYTHEMIA IDIOPATHIC", "Idiopathic thrombocythemia", "idiopathic thrombocythemia", "Essential thrombocythaemia", "hereditary thrombocythemia", "Essential Thrombocythemias", "Idiopathic Thrombocythemias", "Idiopathic thrombocythaemia", "hemorrhagic thrombocythemia", "Hemorrhagic Thrombocythemia", "THROMBOCYTHEMIA, IDIOPATHIC", "Thrombocythemias, Essential", "Thrombocythemia, Idiopathic", "Thrombocythemia, Hemorrhagic", "Thrombocythemias, Idiopathic", "Hemorrhagic Thrombocythemias", "THROMBOCYTHEMIA, HEMORRHAGIC", "[M]Idiopathic thrombocythemia", "Thrombocythemias, Hemorrhagic", "ET - Essential thrombocythemia", "[M]Idiopathic thrombocythaemia", "ET - Essential thrombocythaemia", "primary thrombocytosis (diagnosis)", "Primary hemorrhagic thrombocythemia", "Essential thrombocythemia (disorder)", "essential thrombocytosis (diagnosis)", "THROMBOCYTHEMIA, PRIMARY HEMORRHAGIC", "essential hemorrhagic thrombocythemia", "essential thrombocythemia (diagnosis)", "Primary haemorrhagic thrombocythaemia", "Essential hemorrhagic thrombocythemia", "Idiopathic hemorrhagic thrombocythemia", "idiopathic thrombocythemia (diagnosis)", "Essential haemorrhagic thrombocythaemia", "Essential (hemorrhagic) thrombocythemia", "Idiopathic (hemorrhagic) thrombocythemia", "Idiopathic haemorrhagic thrombocythaemia", "Essential (haemorrhagic) thrombocythaemia", "Essential thrombocythemia (clinical disorder)", "essential hemorrhagic thrombocythemia (diagnosis)", "Essential thrombocythemia (morphologic abnormality)", "THROMBOCYTHEMIA, ESSENTIAL, WITH HEMORRHAGIC DIATHESIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "essential thrombocythemia", "shortest_name_length": 2}
{"curie": "UMLS:C1335047", "names": ["Non-Neoplastic Thyroid Gland Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Thyroid Gland Disorder", "shortest_name_length": 37}
{"curie": "MONDO:0003525", "names": ["gastrinoma", "Gastrinoma", "gastrinomas", "Gastrinomas", "G-Cell Tumor", "G cell tumor", "G Cell Tumor", "G cell tumour", "Gastrinoma NOS", "Gastrinoma, NOS", "G cell tumor, NOS", "[M]Gastrinoma NOS", "G cell tumour, NOS", "Gastrin cell tumor", "Gastrin cell tumour", "Gastrinoma (disorder)", "islet cell gastrinoma", "pancreatic gastrinoma", "Gastrin-Producing NET", "Pancreatic Gastrinoma", "gastrinoma (diagnosis)", "Gastrin Producing Tumor", "Gastrin-Producing Tumor", "Gastrin Secreting Tumor", "gastrin producing tumor", "pancreatic G-cell tumor", "Tumor, Gastrin-Producing", "Gastrin-Producing Tumors", "Tumors, Gastrin-Producing", "Ulcerogenic Islet Cell Tumor", "gastrinoma; unspecified site", "Islet Cell Tumor, Ulcerogenic", "islet cell tumor, ulcerogenic", "G-Cell Gastrin Producing Tumor", "neuroendocrine tumor gastrinoma", "G cell; tumor, unspecified site", "tumor; G cell, unspecified site", "pancreatic gastrin producing NET", "Pancreatic Gastrin Producing NET", "pancreatic gastrin producing tumor", "Pancreatic Gastrin Producing Tumor", "Gastrinoma (morphologic abnormality)", "Gastrin-Producing Neuroendocrine Tumor", "pancreas gastrin-producing neuroendocrine tumor", "Pancreatic Gastrin-Producing Neuroendocrine Tumor", "pancreatic gastrin-producing neuroendocrine tumor", "gastrin-producing neuroendocrine tumor of pancreas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic gastrin-producing neuroendocrine tumor", "shortest_name_length": 10}
{"curie": "UMLS:C0343585", "names": ["Mite-Borne Hemorrhagic Fever", "Mite-borne hemorrhagic fever", "mite-borne hemorrhagic fever", "Mite-borne haemorrhagic fever", "mite-borne hemorrhagic fever (diagnosis)", "Mite-borne hemorrhagic fever (navigational concept)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mite-borne hemorrhagic fever", "shortest_name_length": 28}
{"curie": "MONDO:0013974", "names": ["ECTD6", "ectodermal dysplasia 6", "ECTODERMAL DYSPLASIA 6, HAIR/NAIL TYPE", "ectodermal dysplasia 6, hair/nail type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia 6, hair/nail type", "shortest_name_length": 5}
{"curie": "UMLS:C0086133", "names": ["depressive syndrome", "Depressive Syndrome", "Depressive syndrome", "Syndrome, Depressive", "Depressive Syndromes", "Syndromes, Depressive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Depressive Syndrome", "shortest_name_length": 19}
{"curie": "MONDO:0014959", "names": ["MTDPS12A", "mitochondrial DNA depletion syndrome 12a", "mitochondrial DNA depletion syndrome 12A (cardiomyopathic type) AD", "mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant", "mitochondrial DNA depletion syndrome 12a (cardiomyopathic type), autosomal dominant", "MITOCHONDRIAL DNA DEPLETION SYNDROME 12A (CARDIOMYOPATHIC TYPE), AUTOSOMAL DOMINANT", "mitochondrial DNA depletion syndrome 12a (cardiomyopathic type), autosomal dominant; MTDPS12A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant", "shortest_name_length": 8}
{"curie": "MONDO:0016790", "names": ["TCA cycle disorder", "Krebs cycle disorder", "citric acid cycle disorder", "tricarboxylic acid cycle disorder", "inborn tricarboxylic acid cycle disorder", "inborn error of tricarboxylic acid cycle", "rare inborn error of tricarboxylic acid cycle"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tricarboxylic acid cycle disorder", "shortest_name_length": 18}
{"curie": "MONDO:0011236", "names": ["HHF3", "familial hyperinsulinemic hypoglycemia 3", "hyperinsulinemic hypoglycemia familial 3", "Hyperinsulinemic hypoglycemia, familial, 3", "hyperinsulinemic hypoglycemia, familial, 3", "HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 3", "Hyperinsulinism due to glucokinase deficiency", "hyperinsulinism due to glucokinase deficiency", "hyperinsulinemic hypoglycemia, familial, type 3", "Hyperinsulinism due to deficiency of glucokinase", "Hyperinsulinism due to deficiency of glucokinase (disorder)", "Hyperinsulinemic hypoglycemia due to glucokinase deficiency", "hyperinsulinemic hypoglycemia due to glucokinase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperinsulinism due to glucokinase deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0004367", "names": ["Petroclival Meningioma", "petroclival meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "petroclival meningioma", "shortest_name_length": 22}
{"curie": "MONDO:0006128", "names": ["Anaplastic CNS Large Cell Lymphoma", "anaplastic CNS large cell lymphoma", "anaplastic large cell lymphoma of CNS", "Anaplastic Large Cell Lymphoma of CNS", "anaplastic large cell lymphoma of the CNS", "Anaplastic Large Cell Lymphoma of the CNS", "primary CNS anaplastic large cell lymphoma", "Primary CNS Anaplastic Large Cell Lymphoma", "Anaplastic Central Nervous System Large Cell Lymphoma", "Central Nervous System Anaplastic Large Cell Lymphoma", "anaplastic central nervous system large cell lymphoma", "central nervous system anaplastic large cell lymphoma", "Anaplastic Large Cell Lymphoma of Central Nervous System", "anaplastic large cell lymphoma of central nervous system", "anaplastic large cell lymphoma of the central nervous system", "Anaplastic Large Cell Lymphoma of the Central Nervous System", "Primary Central Nervous System Anaplastic Large Cell Lymphoma", "primary central nervous system anaplastic large cell lymphoma", "anaplastic large cell lymphoma of central nervous system (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system anaplastic large cell lymphoma", "shortest_name_length": 34}
{"curie": "MONDO:0009546", "names": ["macrosomia adiposa congenita", "Macrosomia Adiposa Congenita", "MACROSOMIA ADIPOSA CONGENITA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macrosomia adiposa congenita", "shortest_name_length": 28}
{"curie": "MONDO:0010221", "names": ["CHIME", "GPIBD5", "PIGL-CDG", "CHIME syndrome", "CHIME SYNDROME", "Zunich Kaye syndrome", "Zunich-Kaye syndrome", "ZUNICH NEUROECTODERMAL SYNDROME", "Zunich neuroectodermal syndrome", "Neuroectodermal dysplasia CHIME type", "Neuroectodermal syndrome, Zunich type", "neuroectodermal dysplasia, CHIME type", "neuroectodermal syndrome, Zunich type", "Neuroectodermal dysplasia, CHIME type", "GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 5", "glycosylphosphatidylinositol biosynthesis defect 5", "congenital disorder of glycosylation due to PIGL deficiency", "Congenital disorder of glycosylation due to PIGL deficiency", "coloboma-congenital heart disease-ichthyosiform dermatosis-intellectual disability-ear anomalies syndrome", "Coloboma-congenital heart disease-ichthyosiform dermatosis-intellectual disability-ear anomalies syndrome", "Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome", "COLOBOMA, CONGENITAL HEART DISEASE, ICHTHYOSIFORM DERMATOSIS, MENTAL RETARDATION, AND EAR ANOMALIES SYNDROME", "coloboma, congenital heart disease, ichthyosiform dermatosis, mental retardation, and ear anomalies syndrome", "coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability, and ear anomalies syndrome", "CHIME (coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability, ear anomaly) syndrome", "Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome (disorder)", "Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome (diagnosis)", "COLOBOMA, CONGENITAL HEART DISEASE, ICHTHYOSIFORM DERMATOSIS, IMPAIRED INTELLECTUAL DEVELOPMENT, AND EAR ANOMALIES SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CHIME syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C4054538", "names": ["NEP Induced Membranous Nephropathy", "Membranous Nephropathy - NEP Induced", "Neural Endopeptidase Induced Membranous Nephropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Membranous Nephropathy - NEP Induced", "shortest_name_length": 34}
{"curie": "UMLS:C1334607", "names": ["Liver and Intrahepatic Bile Duct Malignant Non-Epithelial Neoplasm", "Malignant Non-Epithelial Hepatic and Intrahepatic Bile Duct Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liver and Intrahepatic Bile Duct Malignant Non-Epithelial Neoplasm", "shortest_name_length": 66}
{"curie": "MONDO:0019805", "names": ["TTTS", "twin transfusion", "Twin Transfusion", "Transfusion, Twin", "Twin Transfusions", "twin transfusions", "stuck Twin syndrome", "Stuck Twin Syndrome", "Fetofetal Transfusion", "Fetofetal transfusion", "TWIN TWIN TRANSFUSION", "twin twin transfusion", "fetofetal transfusion", "Fetofetal Transfusions", "Transfusion, Fetofetal", "Twin-to-Twin Transfusion", "twin to twin transfusion", "Twin to Twin Transfusion", "Twin-to-twin transfusion", "Twin to twin transfusion", "Twin Transfusion Syndrome", "twin transfusion syndrome", "Transfusion, Twin-to-Twin", "Twin-to-Twin Transfusions", "Fetal Transfusion Syndrome", "Twin Transfusion Syndromes", "fetal transfusion syndrome", "Syndrome, Twin Transfusion", "Transfusion Syndrome, Twin", "Syndrome, Fetal Transfusion", "Transfusion Syndrome, Fetal", "Twin-to-twin blood transfer", "Fetal Transfusion Syndromes", "fetal twin-twin transfusion", "Fetal hemorrhage into co-twin", "fetal hemorrhage into co-twin", "Fetal haemorrhage into co-twin", "Fetal twin to twin transfusion", "Fetofetal transfusion syndrome", "Twin-Twin transfusion syndrome", "twin-twin transfusion syndrome", "syndrome transfusion twin-twin", "Twin Twin Transfusion Syndrome", "Twin-Twin Transfusion Syndrome", "Fetofetal Transfusion Syndrome", "Intrauterine Cross-Transfusion", "Placental Transfusion Syndrome", "syndrome transfusion twin twin", "Twin-twin transfusion syndrome", "Intrauterine Cross Transfusion", "twin twin transfusion syndrome", "placental transfusion syndrome", "Fetofetal Transfusion Syndromes", "Intrauterine Cross-Transfusions", "Transfusion Syndrome, Fetofetal", "Cross-Transfusion, Intrauterine", "Cross Transfusion, Intrauterine", "Feto-fetal transfusion syndrome", "Syndrome, Fetofetal Transfusion", "Twin to twin transfusion syndrome", "twin to twin transfusion syndrome", "Twin-to-Twin Transfusion Syndrome", "twin-to-twin transfusion syndrome", "Twin to Twin Transfusion Syndrome", "Transfusion Syndrome, Twin-to-Twin", "Twin-to-Twin Transfusion Syndromes", "Syndrome, Twin-to-Twin Transfusion", "twin to twin transfusion (diagnosis)", "FFTS - Fetofetal transfusion syndrome", "Twin-to-twin blood transfer (disorder)", "fetal twin-twin transfusion (diagnosis)", "TTTS - Twin to twin transfusion syndrome", "fetus-to-fetus placental transfusion syndrome", "Fetus-to-fetus placental transfusion syndrome", "fetal blood loss from fetal hemorrhage into co-twin", "Fetal blood loss from fetal hemorrhage into co-twin", "fetal conditions hematologic twin to twin transfusion", "fetus-to-fetus placental transfusion syndrome (diagnosis)", "Fetus-to-fetus placental transfusion syndrome, unspecified trimester"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "twin to twin transfusion syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0018103", "names": ["Quinquaud's disease", "Quinquaud’s disease", "Folliculitis depilans", "Folliculitis decalvans", "folliculitis decalvans", "decalvans folliculitis", "folliculitis; decalvans", "decalvans; folliculitis", "Folliculitis decalvans (disorder)", "Quinquaud's decalvans folliculitis", "folliculitis decalvans (diagnosis)", "Quinquaud's folliculitis decalvans"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Quinquaud's folliculitis decalvans", "shortest_name_length": 19}
{"curie": "MONDO:0004092", "names": ["Thymus Basaloid Carcinoma", "Thymic Basaloid Carcinoma", "Thymus basaloid carcinoma", "thymus basaloid carcinoma", "thymic basaloid carcinoma", "basaloid carcinoma of Thymus", "Basaloid Carcinoma of Thymus", "Basaloid carcinoma of the Thymus", "basaloid carcinoma of the Thymus", "Basaloid Carcinoma of the Thymus", "thymus basaloid squamous cell carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thymic basaloid carcinoma", "shortest_name_length": 25}
{"curie": "UMLS:C5235851", "names": ["Recurrent Small Cell Glioblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Small Cell Glioblastoma", "shortest_name_length": 33}
{"curie": "MONDO:0000611", "names": ["pre-malignant neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pre-malignant neoplasm", "shortest_name_length": 22}
{"curie": "MONDO:0002129", "names": ["Bone Cancer", "bone tumour", "Bone cancer", "BONE CANCER", "bone cancer", "bone cancers", "Bones--Cancer", "osseous tumor", "bone neoplasm", "osseous cancer", "Cancer of Bone", "cancer of bone", "Bone Neoplasms", "Osseous Cancer", "Bone cancer NOS", "CA - Bone cancer", "Bone cancer, NOS", "neoplasm of bone", "CA - bone cancer", "Cancer of the Bone", "cancer of the bone", "Malignant bone tumor", "malignant bone tumor", "Malignant Bone Tumor", "malignant bone tumour", "Malignant bone tumour", "bone malignant tumors", "Neoplasm malig;bone(s)", "malignant tumor of bone", "malignant bone neoplasm", "bone cancer (diagnosis)", "Malignant Osseous Tumor", "bone malignant neoplasm", "Bone neoplasm malignant", "skeletal element cancer", "malignant osseous tumor", "Malignant Tumor of Bone", "Malignant Bone Neoplasm", "Malignant Osseous Neoplasm", "cancer of skeletal element", "Malignant neoplasm of bone", "malignant osseous neoplasm", "malignant neoplasm of bone", "Malignant Neoplasm of Bone", "Malignant Tumor of the Bone", "malignant tumor of the bone", "malignant neoplasm of the bone", "Malignant Neoplasm of the Bone", "Malignant neoplasm of bone, NOS", "malignant neosplasm of the bone(s)", "malignant skeletal element neoplasm", "Malignant neoplasm of bone (disorder)", "malignant neoplasm of bone (diagnosis)", "malignant neoplasm of skeletal element"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bone cancer", "shortest_name_length": 11}
{"curie": "MONDO:0024307", "names": ["prothrombin deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prothrombin deficiency", "shortest_name_length": 22}
{"curie": "UMLS:C0270090", "names": ["Caput Succedaneum", "caput succedaneum", "Caput succedaneum", "caput; succedaneum", "succedaneum; caput", "scalp caput succedaneum", "Caput succedaneum (disorder)", "caput succedaneum (diagnosis)", "Swelling edema of scalp during labor", "caput succedaneum (physical finding)", "Swelling oedema of scalp during labour"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Caput succedaneum", "shortest_name_length": 17}
{"curie": "MONDO:0800134", "names": ["primary immunodeficiency due to calcium channel deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary immunodeficiency due to calcium channel deficiency", "shortest_name_length": 58}
{"curie": "OMIM:178800", "names": ["PUPIL, EGG-SHAPED", "Pupil, Egg-Shaped"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 17}
{"curie": "UMLS:C0858899", "names": ["Attention concentration difficulty"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Attention concentration difficulty", "shortest_name_length": 34}
{"curie": "UMLS:C5204119", "names": ["Crystal-Storing Histiocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Crystal-Storing Histiocytosis", "shortest_name_length": 29}
{"curie": "UMLS:C5237244", "names": ["BAP1-Inactivated Melanocytoma", "BAP1-Inactivated Cutaneous Melanocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "BAP1-Inactivated Melanocytoma", "shortest_name_length": 29}
{"curie": "MONDO:0014876", "names": ["MRT54", "intellectual developmental disorder 54", "mental retardation, autosomal recessive 54", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 54", "intellectual disability, autosomal recessive 54", "mental retardation, autosomal recessive type 54", "intellectual disability, autosomal recessive type 54", "autosomal recessive intellectual developmental disorder 54", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 54", "TNIK autosomal recessive non-syndromic intellectual disability", "autosomal recessive non-syndromic intellectual disability caused by mutation in TNIK"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 54", "shortest_name_length": 5}
{"curie": "MONDO:0008260", "names": ["KS", "KNDLRS", "KINDLER SYNDROME", "Kindler syndrome", "KINDLER syndrome", "Kindler's syndrome", "poikiloderma of Kindler", "Poikiloderma of Kindler", "Kindler's syndrome (disorder)", "Kindler epidermolysis bullosa", "Congenital bullous poikiloderma", "congenital bullous poikiloderma", "poikiloderma, hereditary acrokeratotic", "POIKILODERMA, HEREDITARY ACROKERATOTIC", "Poikiloderma, hereditary acrokeratotic", "poikiloderma, congenital, with bullae, Weary type", "POIKILODERMA, CONGENITAL, WITH BULLAE, WEARY TYPE", "Poikiloderma, congenital, with bullae, weary type", "hereditary acrokeratotic poikiloderma of Kindler-Weary", "Bullous acrokeratotic poikiloderma of kindler and weary", "bullous acrokeratotic poikiloderma of Kindler and Weary", "BULLOUS ACROKERATOTIC POIKILODERMA OF KINDLER AND WEARY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kindler syndrome", "shortest_name_length": 2}
{"curie": "MONDO:0043839", "names": ["Ulc", "ulcer", "Ulcus", "ULCER", "Ulcer", "ulcers", "ULCERS", "Ulcers", "ulcerate", "Ulcerated", "ulcerated", "Ulcer NOS", "ulcerates", "Ulceration", "ulceration", "ulcerating", "Ulcerative", "ulcerative", "Ulcerating", "Ulcus, NOS", "Ulcer, NOS", "ulcerations", "ulceratives", "ulcer lesion", "lesions ulcer", "ulcer disease", "Ulcer - lesion", "lesions ulcers", "Ulceration, NOS", "Ulcer (disorder)", "Ulcerative lesion", "Ulcerative lesions", "lesions ulcerative", "Ulcerative lesion, NOS", "Ulcerative (qualifier value)", "Ulcer (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ulcer disease", "shortest_name_length": 3}
{"curie": "UMLS:C5237758", "names": ["Advanced Anaplastic Large Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Anaplastic Large Cell Lymphoma", "shortest_name_length": 39}
{"curie": "MONDO:0013574", "names": ["CUTIS LAXA-MARFANOID SYNDROME", "Cutis Laxa-Marfanoid Syndrome", "Cutis laxa-Marfanoid syndrome", "cutis laxa - Marfanoid syndrome", "Neonatal Cutis Laxa With Marfanoid Phenotype", "Neonatal cutis laxa with marfanoid phenotype", "CUTIS LAXA, NEONATAL, WITH MARFANOID PHENOTYPE", "cutis laxa, neonatal, with MARFANOID phenotype", "Neonatal cutis laxa with marfanoid phenotype (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutis laxa - Marfanoid syndrome", "shortest_name_length": 29}
{"curie": "MONDO:0013971", "names": ["LTBL", "COXPD12", "combined oxidative phosphorylation deficiency 12", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12", "Combined oxidative phosphorylation defect type 12", "combined oxidative phosphorylation defect type 12", "EARS2 combined oxidative phosphorylation deficiency", "combined oxidative phosphorylation deficiency type 12", "COXPD12 - combined oxidative phosphorylation defect type 12", "combined oxidative phosphorylation deficiency caused by mutation in EARS2", "Leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome", "leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome", "leukoencephalopathy thalamus and brainstem anomalies, high lactate syndrome", "Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome", "LEUKOENCEPHALOPATHY WITH THALAMUS AND BRAINSTEM INVOLVEMENT AND HIGH LACTATE", "leukoencephalopathy with thalamus and brainstem involvement and high lactate", "leukoencephalopathy, thalamus, and brainstem anomalies, high lactate syndrome", "Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome (disorder)", "leukoencephalopathy, thalamus, and brainstem anomalies, high lactate syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0010917", "names": ["CCAL1", "CPPDD1", "CHONDROCALCINOSIS 1", "chondrocalcinosis 1", "Chondrocalcinosis 1", "Chondrocalcinosis with early-onset osteoarthritis", "CHONDROCALCINOSIS WITH EARLY-ONSET OSTEOARTHRITIS", "chondrocalcinosis with early-onset osteoarthritis", "CALCIUM PYROPHOSPHATE DIHYDRATE DEPOSITION DISEASE 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chondrocalcinosis 1", "shortest_name_length": 5}
{"curie": "MONDO:0014393", "names": ["LMPH1D", "LMPHM4", "LMPH1D, FORMERLY", "LYMPHATIC MALFORMATION 4", "hereditary lymphedema ID", "lymphatic malformation 4", "lymphedema, hereditary, 1D", "VEGFC hereditary lymphedema", "lymphedema, hereditary, type 1D", "LYMPHEDEMA, HEREDITARY, ID, FORMERLY", "hereditary lymphedema caused by mutation in VEGFC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphatic malformation 4", "shortest_name_length": 6}
{"curie": "UMLS:C3273117", "names": ["Gallbladder G3", "Gallbladder NEC", "Gallbladder Neuroendocrine Cancer", "Gallbladder Neuroendocrine Carcinoma", "Gallbladder High Grade Neuroendocrine Carcinoma", "Gallbladder Poorly Differentiated Endocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gallbladder Neuroendocrine Carcinoma", "shortest_name_length": 14}
{"curie": "UMLS:C5668173", "names": ["Refractory Diffuse Large B-Cell Lymphoma Associated with Chronic Inflammation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Diffuse Large B-Cell Lymphoma Associated with Chronic Inflammation", "shortest_name_length": 77}
{"curie": "MONDO:0036915", "names": ["Benign Ovarian Mucinous Tumor", "benign ovarian mucinous tumor", "Benign Ovarian Mucinous Neoplasm", "benign ovarian mucinous neoplasm", "ovarian mucinous neoplasm, benign"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign ovarian mucinous tumor", "shortest_name_length": 29}
{"curie": "UMLS:C3887520", "names": ["Pineoblastoma", "childhood pineoblastoma", "Childhood Pineoblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Pineoblastoma", "shortest_name_length": 13}
{"curie": "MONDO:0000948", "names": ["xeroma", "EYES DRY", "XEROPHTHALMIA", "xerophthalmia", "xerophthalmus", "Xerophthalmia", "Xerophthalmias", "ophthalmoxerosis", "Xerophthalmia NOS", "conjunctiva; xerosis", "conjunctival xerosis", "xerosis; conjunctiva", "Conjunctival Xerosis", "Conjunctival xerosis", "Tear film insufficiency", "xerophthalmia (etiology)", "Xerophthalmia (disorder)", "xerophthalmia (diagnosis)", "Tear film insufficiency, NOS", "xerophthalmia (manifestation)", "Conjunctival xerosis (disorder)", "conjunctival xerosis (diagnosis)", "Conjunctival xerosis, unspecified", "Tear film insufficiency (disorder)", "Tear film insufficiency, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "xerophthalmia", "shortest_name_length": 6}
{"curie": "MONDO:0003588", "names": ["larynx liposarcoma", "lip larynx sarcoma", "Larynx Liposarcoma", "Laryngeal Liposarcoma", "liposarcoma of larynx", "Liposarcoma of Larynx", "laryngeal liposarcoma", "liposarcoma of the larynx", "Liposarcoma of the Larynx"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "larynx liposarcoma", "shortest_name_length": 18}
{"curie": "MONDO:0006857", "names": ["MCA Infarct", "MCA Infarcts", "Infarct, MCA", "Infarcts, MCA", "MCA Infarction", "mca infarction", "Middle cerebral artery stroke", "middle cerebral artery stroke", "Middle Cerebral Artery Stroke", "Middle cerebral artery infarct", "Stroke, Middle Cerebral Artery", "middle cerebral artery infarct", "stroke of middle cerebral artery", "Middle Cerebral Artery Infarction", "middle cerebral artery infarction", "Infarction, Middle Cerebral Artery", "Cerebral Infarction, Middle Cerebral Artery", "stroke of middle cerebral artery (diagnosis)", "Middle Cerebral Artery Circulation Infarction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "middle cerebral artery infarction", "shortest_name_length": 11}
{"curie": "UMLS:C1882971", "names": ["Salivary Gland Clear Cell Carcinoma", "Salivary Gland Clear Cell Carcinoma, NOS", "Salivary Gland Clear Cell Carcinoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Salivary Gland Clear Cell Carcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C1334429", "names": ["Low Risk Colorectal Gastrointestinal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Risk Colorectal Gastrointestinal Stromal Tumor", "shortest_name_length": 50}
{"curie": "UMLS:C0272692", "names": ["open fracture of shaft of metacarpal bone", "Open fracture of shaft of metacarpal bone", "Open Fracture of Shaft of Metacarpal Bone", "Open fracture of shaft of metacarpal bones", "Open fracture of shaft of metacarpal bone(s)", "Open fracture of shaft of metacarpal bone (disorder)", "open fracture of shaft of metacarpal bone (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Open fracture of shaft of metacarpal bone", "shortest_name_length": 41}
{"curie": "MONDO:0009394", "names": ["JPD", "JPG", "PDB5", "Familial osteoectasia", "Familial Osteoectasia", "familial osteoectasia", "Osteoectasia, familial", "OSTEOECTASIA, FAMILIAL", "osteoectasia, familial", "Juvenile Paget disease", "juvenile Paget disease", "JUVENILE PAGET DISEASE", "Juvenile Paget Disease", "Paget disease of bone-5", "juvenile Pagets disease", "Juvenile Paget's Disease", "Juvenile Paget's disease", "juvenile Paget's disease", "Paget's disease of bone 5", "familial hyperphosphatasia", "Familial Hyperphosphatasia", "Paget disease juvenile type", "Idiopathic Hyperphosphatasia", "Hereditary hyperphosphatasia", "hereditary hyperphosphatasia", "Osteochalasia desmalis familiaris", "Osteochalasia Desmalis Familiaris", "Osteoectasia with hyperphosphatasia", "Osteoectasia with Hyperphosphatasia", "Hyperphosphatasemia with bone disease", "Hyperphosphatasemia with Bone Disease", "hyperphosphatasia, familial idiopathic", "Hyperphosphatasaemia with bone disease", "Hyperphosphatasia, familial idiopathic", "HYPERPHOSPHATASIA, FAMILIAL IDIOPATHIC", "Paget disease of bone 5, juvenile-onset", "PAGET DISEASE OF BONE 5, JUVENILE-ONSET", "Familial Idiopathic Hyperphosphatasemia", "Familial idiopathic hyperphosphatasemia", "Familial idiopathic hyperphosphatasaemia", "hyperostosid corticalis deformans juvenilis", "HYPEROSTOSIS CORTICALIS DEFORMANS JUVENILIS", "hyperostosis corticalis deformans juvenilis", "Hyperostosis corticalis deformans juvenilis", "Hyperphosphatasemia with bone disease (disorder)", "Chronic congenital idiopathic hyperphosphatasemia", "Chronic Congenital Idiopathic Hyperphosphatasemia", "hyperphosphatasemia, chronic congenital idiopathic", "Hyperphosphatasemia, chronic congenital idiopathic", "HYPERPHOSPHATASEMIA, CHRONIC CONGENITAL IDIOPATHIC", "Chronic congenital idiopathic hyperphosphatasaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile Paget disease", "shortest_name_length": 3}
{"curie": "MONDO:0100480", "names": ["Autoimmune Adrenalitis", "autoimmune adrenalitis", "Autoimmune Addison's Disease", "autoimmune Addison's disease", "autoimmune primary adrenal insufficiency", "Autoimmune Primary Adrenal Insufficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune primary adrenal insufficiency", "shortest_name_length": 22}
{"curie": "UMLS:C5420852", "names": ["Ciliary Body Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ciliary Body Adenoma", "shortest_name_length": 20}
{"curie": "UMLS:C0854897", "names": ["Relapsed Malignant Hemangiopericytoma", "Recurrent Malignant Hemangiopericytoma", "Malignant Hemangiopericytoma Recurrent", "Malignant hemangiopericytoma recurrent", "Malignant haemangiopericytoma recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant hemangiopericytoma recurrent", "shortest_name_length": 37}
{"curie": "MONDO:0054862", "names": ["POF15", "PREMATURE OVARIAN FAILURE 15", "premature ovarian failure 15", "primary ovarian insufficiency 15"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "premature ovarian failure 15", "shortest_name_length": 5}
{"curie": "UMLS:C3887605", "names": ["PARONIRIA", "Paroniria", "Nightmare", "Nightmares", "Nightmare, NOS", "Nightmares NOS", "Nightmare disorder", "Nightmare Disorder", "nightmare disorder", "dream anxiety disorder", "Dream anxiety disorder", "dream anxiety disorders", "nightmare disorder (diagnosis)", "Dream anxiety disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nightmare Disorder", "shortest_name_length": 9}
{"curie": "UMLS:C0271663", "names": ["GDM, class A2", "Gestational Diabetes Mellitus, A2", "Gestational diabetes mellitus class A2", "Gestational diabetes mellitus, class A2", "Gestational Diabetes, A2 White Classification", "Gestational diabetes mellitus class A2 (disorder)", "Gestational Diabetes Mellitus, A2 White Classification", "gestational diabetes mellitus, White's classification A2", "gestational diabetes mellitus, White's classification A2 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gestational diabetes mellitus class A2", "shortest_name_length": 13}
{"curie": "MONDO:0009758", "names": ["CSNB1B", "CSNB, COMPLETE, AUTOSOMAL RECESSIVE", "CSNB, complete, autosomal recessive", "congenital stationary night blindness 1B", "GRM6 congenital stationary night blindness", "congenital stationary night blindness type 1B", "Night Blindness, Congenital Stationary, Type 1B", "congenital stationary night blindness - type 1b", "NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B", "night blindness, congenital stationary, type 1B", "congenital stationary night blindness - type 1b (diagnosis)", "congenital stationary night blindness 1B autosomal recessive", "congenital stationary night blindness caused by mutation in GRM6", "autosomal recessive complete congenital stationary night blindness", "NIGHT BLINDNESS, CONGENITAL STATIONARY, COMPLETE, AUTOSOMAL RECESSIVE", "night blindness, congenital stationary, complete, autosomal recessive", "Night Blindness, Congenital Stationary, Complete, Autosomal Recessive", "night blindness, congenital stationary (complete), 1B, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital stationary night blindness 1B", "shortest_name_length": 6}
{"curie": "MONDO:0030927", "names": ["MFM11", "MYOFIBRILLAR MYOPATHY 11", "myofibrillar myopathy 11", "myopathy, congenital, with eccentric cores", "MYOPATHY, CONGENITAL, WITH ECCENTRIC CORES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myofibrillar myopathy 11", "shortest_name_length": 5}
{"curie": "MONDO:0007691", "names": ["GBS", "AIDP", "Familial Guillain-Barre Syndrome", "Inflammatory Polyneuropathy Acute", "GUILLAIN-BARRE SYNDROME, FAMILIAL", "Acute inflammatory polyneuropathy", "Syndrome, Familial Guillain-Barre", "Guillain Barre Syndrome, Familial", "Familial Guillain-Barre Syndromes", "Guillain-Barre Syndrome, Familial", "Guillain-Barre syndrome, familial", "Acute Inflammatory Polyneuropathy", "Inflammatory Polyneuropathy, Acute", "Polyneuropathy Acute, Inflammatory", "Guillain-Barre Syndromes, Familial", "Polyneuropathy, Acute Inflammatory", "Acute Inflammatory Polyneuropathies", "Inflammatory Polyneuropathies, Acute", "neuropathy, inflammatory demyelinating", "Acute Inflammatory Polyradiculoneuropathy", "Polyradiculoneuropathy, Acute Inflammatory", "Acute Inflammatory Polyradiculoneuropathies", "Polyradiculoneuropathies, Acute Inflammatory", "Inflammatory Polyradiculoneuropathies, Acute", "Acute idiopathic demyelinating polyneuropathy", "Acute Inflammatory Demyelinating Polyneuropathy", "Acute inflammatory demyelinating polyneuropathy", "Polyneuropathy, Inflammatory Demyelinating, Acute", "POLYNEUROPATHY, INFLAMMATORY DEMYELINATING, ACUTE", "chronic inflammatory demyelinating polyneuropathy", "polyneuropathy, inflammatory demyelinating, acute", "Acute Inflammatory Demyelinating Polyradiculopathy", "Acute inflammatory demyelinating polyradiculopathy", "Acute inflammatory demyelinating polyradiculoneuropathy", "Acute Inflammatory Demyelinating Polyradiculoneuropathy", "Demyelinating Polyradiculoneuropathy, Acute Inflammatory", "Polyradiculoneuropathy, Acute Inflammatory Demyelinating", "Inflammatory Demyelinating Polyradiculoneuropathy, Acute", "Acute inflammatory demyelinating polyneuropathy (disorder)", "acute inflammatory demyelinating polyradiculoneuropathy (AIDP)", "GBS, acute inflammatory demyelinating polyradiculoneuropathic form", "Guillain-Barré syndrome acute inflammatory demyelinating polyradiculoneuropathic form", "Guillain-Barré syndrome, acute inflammatory demyelinating polyradiculoneuropathic form", "Guillain-Barré syndrome acute inflammatory demyelinating polyradiculoneuropathic form (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Guillain-Barre syndrome, familial", "shortest_name_length": 3}
{"curie": "UMLS:C5419769", "names": ["Digestive System Neuroendocrine Tumor G3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Digestive System Neuroendocrine Tumor G3", "shortest_name_length": 40}
{"curie": "MONDO:0020395", "names": ["valvar pulmonary stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "valvar pulmonary stenosis", "shortest_name_length": 25}
{"curie": "MONDO:0012035", "names": ["Longman-Tolmie syndrome", "Longman Tolmie syndrome", "Craniosynostosis-intracranial calcifications syndrome", "craniosynostosis-intracranial calcifications syndrome", "Craniosynostosis and intracranial calcification syndrome", "Craniosynostosis and intracranial calcification syndrome (disorder)", "craniosynostosis, calcification of basal ganglia, and facial dysmorphism", "CRANIOSYNOSTOSIS, CALCIFICATION OF BASAL GANGLIA, AND FACIAL DYSMORPHISM", "Craniosynostosis, Calcification of Basal Ganglia, and Facial Dysmorphism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniosynostosis-intracranial calcifications syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0016183", "names": ["qualitative or quantitative defects of protein glycosyltransferase-like"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of protein glycosyltransferase-like", "shortest_name_length": 71}
{"curie": "MONDO:0006594", "names": ["PEMPHIGUS", "pemphigus", "Pemphigus", "Pemphigus NOS", "Pemphigus, NOS", "Pemphigus (disorder)", "pemphigus (diagnosis)", "Pemphigus, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pemphigus", "shortest_name_length": 9}
{"curie": "UMLS:C0263283", "names": ["Dermatitis due to poison oak", "Dermatitis due to Rhus diversiloba", "contact dermatitis due to poison oak", "Contact dermatitis due to poison oak", "Allergic dermatitis due to poison oak", "Contact dermatitis caused by poison oak", "dermatitis due to contact with poison oak", "Contact dermatitis due to Rhus diversiloba", "Allergic dermatitis due to Rhus diversiloba", "contact dermatitis due to poison oak (diagnosis)", "Contact dermatitis caused by urushiol from poison oak", "Contact dermatitis caused by Toxicodendron diversilobum", "Contact dermatitis caused by urushiol from Rhus diversiloba", "Contact dermatitis caused by urushiol from Pacific poison oak", "Contact dermatitis caused by urushiol from poison oak (disorder)", "contact dermatitis due to urushiol from Toxicodendron diversilobum", "Contact dermatitis caused by urushiol from Toxicodendron diversilobum", "contact dermatitis due to urushiol from Toxicodendron diversilobum (diagnosis)", "Contact dermatitis caused by urushiol from Toxicodendron diversilobum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Contact dermatitis caused by urushiol from Pacific poison oak", "shortest_name_length": 28}
{"curie": "MONDO:0015095", "names": ["Peters anomaly with cataract", "Peters anomaly-cataract syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peters anomaly-cataract syndrome", "shortest_name_length": 28}
{"curie": "UMLS:C0855198", "names": ["Stage I Supradiaphragmatic Mixed Cellularity Hodgkin Lymphoma", "Hodgkin's disease mixed cellularity stage I supradiaphragmatic", "Stage I Supradiaphragmatic Mixed Cellularity Hodgkin's Disease", "Stage I Mixed Cellularity Hodgkin's Disease above the Diaphragm", "Stage I Supradiaphragmatic Mixed Cellularity Hodgkin's Lymphoma", "Stage I Mixed Cellularity Hodgkin's Lymphoma above the Diaphragm", "Stage I Supradiaphragmatic Mixed Cellularity Classical Hodgkin Lymphoma", "Ann Arbor Stage I Supradiaphragmatic Mixed Cellularity Classic Hodgkin Lymphoma", "Ann Arbor Stage I Supradiaphragmatic Mixed Cellularity Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's disease mixed cellularity stage I supradiaphragmatic", "shortest_name_length": 61}
{"curie": "MONDO:0010953", "names": ["face", "FACE", "FANCE", "FANCE Fanconi anemia", "Fanconi anemia complementation group E", "FANCONI ANEMIA, COMPLEMENTATION GROUP E", "Fanconi anemia, complementation group E", "Fanconi Anemia, Complementation Group E", "Fanconi anemia caused by mutation in FANCE", "Fanconi anemia complementation group type E", "Fanconi Anemia, complementation group type E", "Fanconi anemia complementation group E (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fanconi anemia complementation group E", "shortest_name_length": 4}
{"curie": "MONDO:0004330", "names": ["Sarcoma, Meningeal", "sarcoma, meningeal", "leptomeninx sarcoma", "leptomeninges sarcoma", "sarcoma of leptomeninx", "leptomeningeal sarcoma", "Leptomeningeal Sarcoma", "Leptomeningeal sarcoma", "sarcoma of leptomeninges", "sarcoma of Leptomeninges", "Sarcoma of Leptomeninges", "sarcoma of the leptomeninges", "Sarcoma of the Leptomeninges", "sarcoma, leptomeningeal, malignant", "SARCOMA, LEPTOMENINGEAL, MALIGNANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leptomeningeal sarcoma", "shortest_name_length": 18}
{"curie": "MONDO:0045059", "names": ["cribriform carcinoma", "cribriform carcinoma of breast", "ductal carcinoma, cribriform type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cribriform carcinoma of breast", "shortest_name_length": 20}
{"curie": "UMLS:C0349217", "names": ["depressive episode", "Depressive episode", "episode; depressive", "depressive; episode", "Episode of depression", "depressive episode (diagnosis)", "Episode of depression (finding)", "Depressive episode, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Depressive episode, unspecified", "shortest_name_length": 18}
{"curie": "UMLS:C2064402", "names": ["Liver Epithelioid Hemangioendothelioma", "Hepatic Epithelioid Hemangioendothelioma", "hepatic epithelioid hemangioendothelioma", "Epithelioid hemangioendothelioma of liver", "Epithelioid haemangioendothelioma of liver", "malignant epithelioid hemangioendothelioma of liver", "Epithelioid hemangioendothelioma of liver (disorder)", "malignant epithelioid hemangioendothelioma of liver (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epithelioid hemangioendothelioma of liver", "shortest_name_length": 38}
{"curie": "UMLS:C1392207", "names": ["Central nervous system necrosis", "necrosis; central nervous system", "central nervous system; necrosis", "Central Nervous System Necrotic Lesion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Necrotic Lesion", "shortest_name_length": 31}
{"curie": "UMLS:C0013781", "names": ["ELECTRIC SHOCK", "electric shock", "Electric shock", "Electric Shock", "Shock;electric", "electric shocks", "electric injury", "Electric injury", "Electric Injury", "Electrical shock", "Injury, Electric", "electric injuries", "electrical injury", "Electric Injuries", "Injuries, Electric", "electrical injuries", "Electrical injuries", "Electrical Injuries", "Electric shock effect", "effects electric shock", "Shock from electric current", "Adverse effect;electric shock", "Injury due to electrical exposure", "Injury caused by electrical exposure", "Injury caused by electrical exposure (disorder)", "Exposure to electric current, with passage of current through tissue", "Exposure to electric current, with passage of current through tissue (event)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Shock from electric current", "shortest_name_length": 14}
{"curie": "MONDO:0000837", "names": ["Bone Resorption", "bone resorption disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bone resorption disease", "shortest_name_length": 15}
{"curie": "UMLS:C4727218", "names": ["Metastatic Cervical Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Cervical Squamous Cell Carcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0044783", "names": ["solid papillary breast carcinoma", "Breast Solid Papillary Carcinoma", "Solid Papillary Breast Carcinoma", "solid Papillary breast carcinoma", "solid Papillary carcinoma of the breast", "Solid Papillary Carcinoma of the Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "solid papillary breast carcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C1334578", "names": ["Malignant Esophageal Neoplasm by Anatomic Region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Esophageal Neoplasm by Anatomic Region", "shortest_name_length": 48}
{"curie": "MONDO:0011160", "names": ["DFNB15", "DFMB15", "DFNB95", "DFNB72", "autosomal recessive deafness 95", "autosomal recessive deafness 15", "autosomal recessive deafness 72", "deafness, autosomal recessive 15", "DEAFNESS, AUTOSOMAL RECESSIVE 72", "deafness, autosomal recessive 72", "deafness, autosomal recessive 95", "Deafness, Autosomal Recessive 15", "DEAFNESS, AUTOSOMAL RECESSIVE 15", "DEAFNESS, AUTOSOMAL RECESSIVE 95", "deafness, autosomal recessive type 15", "autosomal recessive nonsyndromic deafness 15", "GIPC3 autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 15", "autosomal recessive nonsyndromic deafness type 15", "autosomal recessive nonsyndromic deafness caused by mutation in GIPC3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 15", "shortest_name_length": 6}
{"curie": "MONDO:0006907", "names": ["Infundibuloisthmicoma", "pilar sheath acanthoma", "Pilar Sheath Acanthoma", "Pilar sheath acanthoma", "Acanthoma, Pilar Sheath", "Pilar Sheath Acanthomas", "Acanthomas, Pilar Sheath", "Acanthoma of Pilar Sheath", "acanthoma of Pilar sheath", "acanthoma of the Pilar sheath", "Acanthoma of the Pilar Sheath", "Pilar sheath acanthoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pilar sheath acanthoma", "shortest_name_length": 21}
{"curie": "UMLS:C1335025", "names": ["Non-Neoplastic Oral Cavity Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Oral Cavity Disorder", "shortest_name_length": 35}
{"curie": "MONDO:0003215", "names": ["malignant Apocrine tumor", "Malignant Apocrine Tumor", "malignant apocrine tumor", "Malignant Apocrine Neoplasm", "malignant apocrine neoplasm", "apocrine sweat gland cancer", "malignant apocrine skin tumor", "Malignant Apocrine Skin Tumor", "cancer of apocrine sweat gland", "Malignant Apocrine Skin Neoplasm", "malignant apocrine tumor of skin", "malignant apocrine skin neoplasm", "Malignant Apocrine Tumor of Skin", "Malignant Apocrine Neoplasm of Skin", "malignant apocrine neoplasm of skin", "Malignant Apocrine Tumor of the Skin", "malignant apocrine tumor of the skin", "malignant apocrine neoplasm of the skin", "Malignant Apocrine Neoplasm of the Skin", "malignant apocrine sweat gland neoplasm", "malignant neoplasm of apocrine sweat gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "apocrine sweat gland cancer", "shortest_name_length": 24}
{"curie": "UMLS:C0151773", "names": ["marrow hypoplasia", "Marrow depression", "Marrow hypoplasia", "MARROW HYPOPLASIA", "MARROW DEPRESSION", "Hypoplastic marrow", "hypocellular marrow", "Hypocellular marrow", "Marrow depression of", "MARROW DEPRESSION OF", "hypoplasia medullary", "Medullary hypoplasia", "hypoplasia; medullary", "medullary; hypoplasia", "Bone Marrow Hypoplasia", "HYPOPLASIA BONE MARROW", "Hypoplasia bone marrow", "bone depression marrow", "bone marrow hypoplasia", "bone hypoplasia marrow", "BONE MARROW DEPRESSION", "Bone marrow depression", "bone marrow depression", "hypoplasia bone marrow", "Bone marrow hypoplasia", "depression; bone marrow", "bone marrow; depression", "bone marrow; hypoplasia", "hypoplasia; bone marrow", "hypocellular bone marrow", "Hypocellular bone marrow", "bone hypocellular marrow", "Hypocellular Bone Marrow", "BONE MARROW HYPOCELLULAR", "Bone marrow hypocellular", "Hypoplasia of bone marrow", "Bone marrow depression NOS", "Depression bone marrow (NOS)", "DEPRESSION BONE MARROW (NOS)", "Bone marrow depression (disorder)", "Hypocellular bone marrow (finding)", "Hypocellular bone marrow (lab test)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone marrow depression", "shortest_name_length": 17}
{"curie": "UMLS:C5557347", "names": ["Vulvar Squamous Cell Carcinoma, NOS", "Vulvar Squamous Cell Carcinoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Squamous Cell Carcinoma, Not Otherwise Specified", "shortest_name_length": 35}
{"curie": "UMLS:C4054364", "names": ["Syphilis Associated Nephrotic Syndrome", "Nephrotic Syndrome - Syphilis Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - Syphilis Associated", "shortest_name_length": 38}
{"curie": "MONDO:0012738", "names": ["LQT11", "LQT11 (diagnosis)", "long QT syndrome 11", "LONG QT SYNDROME 11", "Long Qt Syndrome 11", "AKAP9 long QT syndrome", "long QT syndrome type 11", "long QT syndrome caused by mutation in AKAP9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "long QT syndrome 11", "shortest_name_length": 5}
{"curie": "UMLS:C1706922", "names": ["Benign Germinative Follicular Epithelium Tumor", "Benign Germinative Follicular Epithelium Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Germinative Follicular Epithelium Neoplasm", "shortest_name_length": 46}
{"curie": "MONDO:0017849", "names": ["Siegler Brewer Carey syndrome", "Siegler-Brewer-Carey syndrome", "Siegler Brewer Carey syndrome (disorder)", "fatal multisystem syndrome involving the eyes, ears, lungs, intestines, and kidneys"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Siegler-Brewer-Carey syndrome", "shortest_name_length": 29}
{"curie": "MONDO:0012880", "names": ["HH5", "KAL5", "Kallmann syndrome 5", "Kallmann Syndrome 5", "KALLMANN SYNDROME 5 (disorder)", "CHD7 hypogonadotropic hypogonadism", "HYPOGONADOTROPIC HYPOGONADISM 5 WITH OR WITHOUT ANOSMIA", "hypogonadotropic hypogonadism 5 with or without anosmia", "hypogonadotropic hypogonadism caused by mutation in CHD7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadotropic hypogonadism 5 with or without anosmia", "shortest_name_length": 3}
{"curie": "MONDO:0800043", "names": ["SWS", "STWS", "SJS2", "Stws", "STWS1", "Stuve-Wiedemann syndrome", "Stüve-Wiedemann syndrome", "STUVE-WIEDEMANN SYNDROME", "STUVE-Wiedemann syndrome", "Stuve-Wiedemann dysplasia", "Stüve-Wiedemann dysplasia", "STUVE-WIEDEMANN SYNDROME 1", "Stüve-Wiedemann syndrome 1", "Schwartz-Jampel syndrome type 2", "Schwartz Jampel type 2 syndrome", "Schwartz-Jampel Syndrome, Type 2", "Schwartz-Jampel syndrome, type 2", "SCHWARTZ-JAMPEL SYNDROME, TYPE 2", "Neonatal Schwartz-Jampel syndrome", "neonatal Schwartz-Jampel syndrome", "Schwartz-Jampel syndrome neonatal", "Schwartz Jampel syndrome neonatal", "SCHWARTZ-JAMPEL SYNDROME, NEONATAL", "Schwartz-Jampel Syndrome, Neonatal", "Schwartz-Jampel syndrome, neonatal", "Stuve-Wiedemann (SW) syndrome (SWS)", "Stuve-Wiedemann dysplasia (disorder)", "neonatal Schwartz-Jampel syndrome type 2", "Stuve-Wiedemann/Schwartz-Jampel type 2 syndrome", "Stüve-Wiedemann/Schwartz-Jampel type 2 syndrome", "Stuve-Wiedemann-Schwartz-Jampel type 2 syndrome", "STUVE-WIEDEMANN/SCHWARTZ-JAMPEL TYPE 2 SYNDROME", "Stuve-Wiedemann syndrome/Schwartz-Jampel type 2 syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stüve-Wiedemann syndrome 1", "shortest_name_length": 3}
{"curie": "MONDO:0012456", "names": ["CPA", "CPAK", "ASGD2", "Lens agenesis", "agenesis; lens", "lens; agenesis", "Agenesis of lens", "Congenital aphakia", "congenital aphakia", "Congenital Aphakia", "Aphakia congenital", "congenital; aphakia", "aphakia; congenital", "Aphakia, congenital", "lens; absence, congenital", "absence; lens, congenital", "congenital primary aphakia", "Congenital primary aphakia", "Congenital absence of lens", "congenital absence of lens", "aphakia, congenital primary", "APHAKIA, CONGENITAL PRIMARY", "Aphakia, congenital primary", "anterior segment dysgenesis 2", "ANTERIOR SEGMENT DYSGENESIS 2", "Congenital aphakia (disorder)", "congenital aphakia (diagnosis)", "anterior segment dysgenesis 2, multiple subtypes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital primary aphakia", "shortest_name_length": 3}
{"curie": "MONDO:0014776", "names": ["SCA42", "SPINOCEREBELLAR ATAXIA 42", "cerebellar ataxia type 42", "spinocerebellar ataxia 42", "Spinocerebellar Ataxia Type 42", "Spinocerebellar ataxia type 42", "spinocerebellar ataxia type 42", "Spinocerebellar ataxia type 42 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia type 42", "shortest_name_length": 5}
{"curie": "MONDO:0011500", "names": ["Becker Nevus Syndrome", "Becker nevus syndrome", "BECKER NEVUS SYNDROME", "hairy epidermal nevus syndrome", "Pigmentary hairy epidermal nevus", "pigmentary hairy epidermal nevus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Becker nevus syndrome", "shortest_name_length": 21}
{"curie": "MONDO:0000594", "names": ["PDD", "Autistic continuum", "Autism spectrum disorder", "autistic spectrum disorder", "Autistic spectrum disorder", "autistic disorders spectrum", "Pervasive Development Disorder", "pervasive development disorder", "development disorder pervasive", "pervasive development disorders", "Pervasive Development Disorders", "Pervasive developmental disorder", "Pervasive Developmental Disorder", "pervasive developmental disorder", "developmental disorder pervasive", "developmental disorder; pervasive", "developmental disorders pervasive", "Pervasive developmental disorders", "Developmental disorder, pervasive", "Pervasive Developmental Disorders", "pervasive; developmental disorder", "pervasive developmental disorders", "Pervasive developmental disorder NOS", "Pervasive developmental disorder, NOS", "pervasive child development disorders", "Pervasive Child Development Disorders", "Pervasive developmental disorder (PDD)", "Child Development Disorders, Pervasive", "PPD - Pervasive developmental disorder", "Pervasive developmental disorder (disorder)", "Unspecified pervasive developmental disorder", "pervasive developmental disorders (diagnosis)", "Pervasive developmental disorder, unspecified", "Other specified early childhood psychoses, current or active state", "Other specified pervasive developmental disorders, current or active state"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pervasive developmental disorder", "shortest_name_length": 3}
{"curie": "UMLS:C0348868", "names": ["Listerial endocarditis", "Listerial endocarditis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Listerial endocarditis", "shortest_name_length": 22}
{"curie": "MONDO:0002558", "names": ["MSCHW", "melanotic neurinoma", "Melanotic Neurinoma", "Pigmented Schwannoma", "Melanotic Schwannoma", "pigmented schwannoma", "Melanotic schwannoma", "Pigmented Schawnnoma", "Pigmented schwannoma", "melanotic schwannoma", "melanotic neurilemmoma", "melanocytic schwannoma", "Melanocytic Schwannoma", "pigmented neurilemmoma", "Melanotic neurilemmoma", "Pigmented Neurilemmoma", "Melanotic Neurilemmoma", "Melanocytic Neurilemmoma", "melanocytic neurilemmoma", "Melanotic schwannoma (disorder)", "Melanotic schwannoma (morphologic abnormality)", "melanotic schwannoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melanotic neurilemmoma", "shortest_name_length": 5}
{"curie": "UMLS:C1520075", "names": ["Vulvar Cellular Angiofibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Cellular Angiofibroma", "shortest_name_length": 28}
{"curie": "MONDO:0014370", "names": ["PCH2E", "pontocerebellar hypoplasia type 2E", "pontocerebellar hypoplasia, type 2E", "PONTOCEREBELLAR HYPOPLASIA, TYPE 2E", "VPS53 non-syndromic pontocerebellar hypoplasia", "non-syndromic pontocerebellar hypoplasia caused by mutation in VPS53"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pontocerebellar hypoplasia type 2E", "shortest_name_length": 5}
{"curie": "MONDO:0017050", "names": ["orbital medulloepithelioma", "Orbital medulloepithelioma", "Intraocular medulloepithelioma", "intraocular medulloepithelioma", "Intraocular Medulloepithelioma", "Ciliary Body Medulloepithelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intraocular medulloepithelioma", "shortest_name_length": 26}
{"curie": "MONDO:0002400", "names": ["SYNOVITIS", "synovitis", "Synovitis", "Synovitides", "Synovitis NOS", "Synovitis, NOS", "synovitis (disease)", "Synovitis (disorder)", "synovitis (diagnosis)", "synovial membrane of synovial joint inflammation", "inflammation of synovial membrane of synovial joint"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "synovitis", "shortest_name_length": 9}
{"curie": "MONDO:0015393", "names": ["nasal ganglioglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasal ganglioglioma", "shortest_name_length": 19}
{"curie": "MONDO:0030043", "names": ["CDG2T", "CDGIIt", "Cdg Iit", "CDG IIt", "congenital disorder of glycosylation, type iit", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIt"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital disorder of glycosylation, type iit", "shortest_name_length": 5}
{"curie": "MONDO:0017878", "names": ["Chapare virus infection", "Chapare hemorrhagic fever", "Chapare haemorrhagic fever", "Hemorrhagic fever caused by Chapare virus", "Haemorrhagic fever caused by Chapare virus", "Hemorrhagic fever caused by Chapare virus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chapare hemorrhagic fever", "shortest_name_length": 23}
{"curie": "MONDO:0011081", "names": ["Collins-Pope syndrome", "Collins Pope syndrome", "dislocation of the hip dysmorphism", "Dislocation of the hip-dysmorphism syndrome", "dislocation of the hip-dysmorphism syndrome", "Dislocation of hip with dysmorphism syndrome", "Dislocation of hip and facial dysmorphism syndrome", "Dislocation of hip and facial dysmorphism syndrome (disorder)", "DISLOCATION OF HIP, CONGENITAL, WITH HYPEREXTENSIBILITY OF FINGERS AND FACIAL DYSMORPHISM", "Hip, Congenital Dislocation of, with Hyperextensibility of Fingers and Facial Dysmorphism", "HIP, CONGENITAL DISLOCATION OF, WITH HYPEREXTENSIBILITY OF FINGERS AND FACIAL DYSMORPHISM", "dislocation of hip, congenital, with hyperextensibility of fingers and facial dysmorphism", "hip, congenital dislocation of, with hyperextensibility of fingers and Facial Dysmorphism", "Dislocation of Hip, Congenital, with Hyperextensibility of Fingers and Facial Dysmorphism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dislocation of the hip-dysmorphism syndrome", "shortest_name_length": 21}
{"curie": "UMLS:C0265615", "names": ["anomaly; hip", "hip; anomaly", "Congenital hip deformity", "deformity; hip, congenital", "Congenital deformity of hip", "Congenital Deformity of Hip", "Congenital hip deformity NOS", "HIP DEFORMITY CONGENITAL NOS", "Congenital deformities of hip", "Congenital deformity of hip joint", "Congenital deformity of hip joint, NOS", "Congenital deformity of hip, unspecified", "Congenital deformity of hip joint (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital deformity of hip joint", "shortest_name_length": 12}
{"curie": "UMLS:C0570562", "names": ["Contrast media allergy", "Allergy to contrast media", "Allergy to contrast media (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Contrast media allergy", "shortest_name_length": 22}
{"curie": "UMLS:C4682443", "names": ["Transformed Follicular Lymphoma to Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transformed Follicular Lymphoma to Diffuse Large B-Cell Lymphoma", "shortest_name_length": 64}
{"curie": "UMLS:C0021386", "names": ["Caseating granuloma", "caseating granuloma", "caseating granulomas", "Necrotising granuloma", "necrotizing granuloma", "Necrotizing granuloma", "Necrotizing Granuloma", "Non-healing granuloma", "Granuloma, necrotizing", "granulomas necrotizing", "Caseating granulomatous inflammation", "Necrotizing granulomatous inflammation", "Necrotising granulomatous inflammation", "Inflammation, necrotizing granulomatous", "Necrotizing Granulomatous Inflammations", "Caseating granulomatous inflammation, NOS", "Necrotizing granulomatous inflammation, NOS", "Necrotizing granulomatous inflammation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Necrotizing granulomatous inflammation", "shortest_name_length": 19}
{"curie": "UMLS:C0851922", "names": ["Peritoneal and Retroperitoneal Disease", "Peritoneal and Retroperitoneal Disorder", "peritoneal and retroperitoneal disorders", "Peritoneal and retroperitoneal disorders", "peritoneal and retroperitoneal disorders (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peritoneal and retroperitoneal disorders", "shortest_name_length": 38}
{"curie": "UMLS:C5668439", "names": ["Recurrent Indolent T-Cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Indolent T-Cell Non-Hodgkin Lymphoma", "shortest_name_length": 46}
{"curie": "UMLS:C4726606", "names": ["Mixed Phenotype Acute Leukemia, B/T/Myeloid, NOS", "Mixed Phenotype Acute Leukemia, B/T/Myeloid, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mixed Phenotype Acute Leukemia, B/T/Myeloid, Not Otherwise Specified", "shortest_name_length": 48}
{"curie": "UMLS:C4288960", "names": ["High Grade Fallopian Tube Serous Carcinoma", "High Grade Fallopian Tube Serous Adenocarcinoma", "Fallopian Tube High-Grade Serous Adenocarcinoma", "Fallopian Tube High Grade Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fallopian Tube High Grade Serous Adenocarcinoma", "shortest_name_length": 42}
{"curie": "OMIM:247150", "names": ["LIP PRINTS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 10}
{"curie": "MONDO:0014154", "names": ["CMTRIC", "RI-CMTC", "RI-CMT type C", "PLEKHG5 Charcot-Marie-Tooth disease", "Charcot-Marie-Tooth disease recessive intermediate C", "CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE C", "Charcot-Marie-Tooth disease, recessive intermediate C", "CHARCOT-MARIE-TOOTH NEUROPATHY, RECESSIVE INTERMEDIATE C", "Charcot-Marie-Tooth neuropathy, recessive Intermediate C", "Charcot-Marie-Tooth disease recessive intermediate type C", "Charcot-Marie-Tooth disease caused by mutation in PLEKHG5", "Charcot-Marie-Tooth disease, recessive Intermediate type C", "autosomal recessive intermediate Charcot-Marie-Tooth disease type C"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease recessive intermediate C", "shortest_name_length": 6}
{"curie": "UMLS:C4682580", "names": ["Stage IB Uterine Corpus Adenosarcoma", "Stage IB Uterine Corpus Adenosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Uterine Corpus Adenosarcoma AJCC v8", "shortest_name_length": 36}
{"curie": "UMLS:C5446664", "names": ["Locally Advanced Malignant Glomus Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Malignant Glomus Tumor", "shortest_name_length": 39}
{"curie": "UMLS:C1518571", "names": ["Omentum EGIST", "Omentum Gastrointestinal Stromal Tumor", "Omentum Extragastrointestinal Stromal Tumor", "Omentum Gastrointestinal Stromal Tumor (GIST)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Omentum Gastrointestinal Stromal Tumor", "shortest_name_length": 13}
{"curie": "MONDO:0010960", "names": ["PCDH3", "Pcdh3", "protocadherin 3", "PROTOCADHERIN 3", "protocadherin type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "protocadherin 3", "shortest_name_length": 5}
{"curie": "UMLS:C1740836", "names": ["Acute migraine", "Acute migraine (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute migraine", "shortest_name_length": 14}
{"curie": "UMLS:C1317977", "names": ["Epithelialization", "epithelialization", "epithelialisation", "Epithelial metaplasia", "Epithelial Metaplasia", "Epithelial Metaplasias", "Metaplasia, epithelial", "Epithelialization, NOS", "EPITHELIAL METAPLASIAS", "Epithelial metaplasia, NOS", "Epithelial metaplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epithelial metaplasia", "shortest_name_length": 17}
{"curie": "MONDO:0800147", "names": ["hemophagocytic lymphohistiocytosis due to RhoG deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemophagocytic lymphohistiocytosis due to RhoG deficiency", "shortest_name_length": 57}
{"curie": "MONDO:0007050", "names": ["Rosenthal-Klöpfer syndrome", "ROSENTHAL-KLOEPFER SYNDROME", "Rosenthal-Kloepfer syndrome", "acromegaly-cutis verticis gyrata-corneal leukoma syndrome", "Acromegaloid changes, cutis verticis gyrata and corneal leukoma", "acromegaloid changes, cutis verticis gyrata and corneal leukoma", "ACROMEGALOID CHANGES, CUTIS VERTICIS GYRATA, AND CORNEAL LEUKOMA", "Acromegaloid Changes, Cutis Verticis Gyrata, And Corneal Leukoma", "acromegaloid changes, cutis verticis gyrata, and corneal leukoma", "Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma", "Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acromegaloid changes, cutis verticis gyrata, and corneal leukoma", "shortest_name_length": 26}
{"curie": "MONDO:0000480", "names": ["anismus", "Anismus", "Anismus (disorder)", "puborectalis syndrome", "dyssynergic defecation", "dyskinetic puborectalis", "Rectosphincteric dyssynergia", "rectosphincteric dyssynergia", "spastic pelvic floor syndrome", "Spastic pelvic floor syndrome", "Sphinteric disobedience syndrome", "Sphincteric disobedience syndrome", "sphincteric disobedience syndrome", "anal region skeletal muscle focal dystonia", "focal dystonia of anal region skeletal muscle"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anismus", "shortest_name_length": 7}
{"curie": "UMLS:C4528554", "names": ["Stage II Breast Cancer", "Anatomic Stage II Breast Cancer AJCC v8", "Anatomic Stage II Breast Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anatomic Stage II Breast Cancer AJCC v8", "shortest_name_length": 22}
{"curie": "UMLS:C4526912", "names": ["Non-keratinizing squamous cell carcinoma", "Non-Keratinizing Squamous Cell Lung Carcinoma", "Lung Non-Keratinizing Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Non-Keratinizing Squamous Cell Carcinoma", "shortest_name_length": 40}
{"curie": "UMLS:C0521190", "names": ["Atypical gastric metaplasia", "Atypical Gastric Metaplasia", "Atypical gastric metaplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypical gastric metaplasia", "shortest_name_length": 27}
{"curie": "UMLS:C5552818", "names": ["Recurrent Pilocytic Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Pilocytic Astrocytoma", "shortest_name_length": 31}
{"curie": "MONDO:0011701", "names": ["IBD4", "inflammatory bowel disease 4", "INFLAMMATORY BOWEL DISEASE 4", "Inflammatory Bowel Disease 4", "inflammatory bowel disease type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory bowel disease 4", "shortest_name_length": 4}
{"curie": "MONDO:0015425", "names": ["lethal recessive chondrodysplasia", "Lethal recessive chondrodysplasia", "chondrodysplasia lethal recessive", "Maroteaux Stanescu Cousin syndrome", "Maroteaux-Stanescu-Cousin syndrome", "Lethal recessive chondrodysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal recessive chondrodysplasia", "shortest_name_length": 33}
{"curie": "MONDO:0000536", "names": ["pharynx squamous cell carcinoma", "Pharyngeal squam. cell carcinoma", "pharyngeal squam. cell carcinoma", "PHARYNGEAL CARCINOMA SQUAMOUS CELL", "pharyngeal squamous cell carcinoma", "Squamous cell carcinoma of pharynx", "Pharyngeal Squamous Cell Carcinoma", "squamous cell carcinoma of pharynx", "Cancer of the pharynx, squamous cell", "Pharyngeal Throat Squamous Cell Cancer", "pharyngeal throat squamous cell cancer", "Squamous cell carcinoma of pharynx (disorder)", "squamous cell carcinoma of pharynx (diagnosis)", "Pharyngeal (including Hypopharyngeal and Oropharyngeal) squamous cell carcinoma", "pharyngeal (including hypopharyngeal and oropharyngeal) squamous cell carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pharyngeal squamous cell carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0020301", "names": ["Prader-Willi syndrome due to paternal 15q11q13 deletion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prader-Willi syndrome due to paternal 15q11q13 deletion", "shortest_name_length": 55}
{"curie": "OMIM:146850", "names": ["IS", "ISCW", "ISSCW", "IMMUNE SUPPRESSION", "STREPTOCOCCAL CELL WALL ANTIGEN, SUPPRESSION OF IMMUNE RESPONSE TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 2}
{"curie": "MONDO:0012039", "names": ["MCI1", "susceptibility to myocardial infarction", "MYOCARDIAL INFARCTION, SUSCEPTIBILITY TO", "myocardial infarction, susceptibility to", "myocardial infarction, protection against", "MYOCARDIAL INFARCTION, PROTECTION AGAINST", "MYOCARDIAL INFARCTION, SUSCEPTIBILITY TO, 1", "myocardial infarction, susceptibility to, 1", "myocardial infarction, decreased susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myocardial infarction, susceptibility to", "shortest_name_length": 4}
{"curie": "UMLS:C5206837", "names": ["Benign Retropharyngeal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Retropharyngeal Neoplasm", "shortest_name_length": 31}
{"curie": "MONDO:0018821", "names": ["X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability", "X-linked facial dysmorphism-short stature-choanal atrsia-intellectual disability syndrome limited to females", "X-linked facial dysmorphism-short stature-choanal atresia-intellectual disability syndrome limited to females"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability", "shortest_name_length": 99}
{"curie": "MONDO:0009263", "names": ["GAPOS", "Gapo Syndrome", "gapo syndrome", "GAPO syndrome", "GAPO SYNDROME", "Odontotrichomelic Syndrome", "Growth delay-alopecia-pseudoanodontia-optic atrophy syndrome", "growth delay-alopecia-pseudoanodontia-optic atrophy syndrome", "Growth retardation, alopecia, pseudoanodontia, optic atrophy", "Growth retardation, alopecia, pseudoanodontia and optic atrophy", "Growth retardation, Alopecia, Pseudoanodontia and Optic atrophy", "Growth Retardation, Alopecia, Pseudoanodontia, And Optic Atrophy", "GROWTH RETARDATION, ALOPECIA, PSEUDOANODONTIA, AND OPTIC ATROPHY", "Growth retardation, alopecia, pseudoanodontia, and optic atrophy", "GAPO - Growth retardation, alopecia, pseudoanodontia, optic atrophy", "Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome", "growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome", "GAPO (growth retardation, alopecia, pseudoanodontia, optic atrophy) syndrome", "Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome (disorder)", "growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome (diagnosis)", "Tetramelic Deficiencies, Ectodermal Dysplasia, Deformed Ears, And Other Abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "GAPO syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0851955", "names": ["Dental Pain and Sensation Disorder", "Dental pain and sensation disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dental pain and sensation disorders", "shortest_name_length": 34}
{"curie": "MONDO:0009970", "names": ["RTD", "renal tubular dysgenesis", "primitive renal tubule syndrome", "genetic renal tubular dysgenesis", "renal tubular dysgenesis of genetic origin", "Renal Tubular Dysgenesis With Choanal Atresia And Athelia", "renal tubular dysgenesis with choanal atresia and athelia", "RENAL TUBULAR DYSGENESIS WITH CHOANAL ATRESIA AND ATHELIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal tubular dysgenesis of genetic origin", "shortest_name_length": 3}
{"curie": "UMLS:C5419208", "names": ["Refractory Lung Non-Small Cell Squamous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Lung Non-Small Cell Squamous Carcinoma", "shortest_name_length": 49}
{"curie": "UMLS:C5205549", "names": ["Metastatic Ovarian Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Ovarian Serous Adenocarcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0010098", "names": ["Taurodont", "Bull teeth", "Taurodontia", "Taurodontism", "taurodontism", "TAURODONTISM", "taurodontism (disease)", "Taurodontism (disorder)", "taurodontism (diagnosis)", "Large elongated pulp chamber", "large pulp chambers in the molars", "Large pulp chambers, in the molars"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "taurodontism", "shortest_name_length": 9}
{"curie": "MONDO:0005592", "names": ["smooth surface dental caries"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "smooth surface dental caries", "shortest_name_length": 28}
{"curie": "UMLS:C4526908", "names": ["Soft Tissue Sarcoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Soft Tissue Sarcoma by AJCC v7 Stage", "shortest_name_length": 36}
{"curie": "MONDO:0013335", "names": ["Tst1", "TST1", "TST REACTIVITY, ABSENCE OF", "tst reactivity, absence of", "tuberculin skin test reactivity, absence of", "TUBERCULIN SKIN TEST REACTIVITY, ABSENCE OF", "TUBERCULIN SKIN TEST REACTIVITY, ABSENCE OF (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tuberculin skin test reactivity, absence of", "shortest_name_length": 4}
{"curie": "MONDO:0019999", "names": ["intestinal malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intestinal malformation", "shortest_name_length": 23}
{"curie": "UMLS:C4725803", "names": ["Recurrent Malignant Female Reproductive System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Malignant Female Reproductive System Neoplasm", "shortest_name_length": 55}
{"curie": "UMLS:C1709503", "names": ["Pericardial Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pericardial Germ Cell Tumor", "shortest_name_length": 27}
{"curie": "MONDO:0004893", "names": ["hypertropia", "Hypertropia", "Hypertropias", "Hypertropia (disorder)", "hypertropia (diagnosis)", "nonparalytic hypertropia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertropia", "shortest_name_length": 11}
{"curie": "UMLS:C1332935", "names": ["Chest Wall Plexiform Fibrohistiocytic Tumor", "Chest Wall Plexiform Fibrohistiocytic Neoplasm", "Plexiform Fibrohistiocytic Tumor of Chest Wall", "Plexiform Fibrohistiocytic Neoplasm of Chest Wall", "Plexiform Fibrohistiocytic Tumor of the Chest Wall", "Plexiform Fibrohistiocytic Neoplasm of the Chest Wall"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chest Wall Plexiform Fibrohistiocytic Tumor", "shortest_name_length": 43}
{"curie": "UMLS:C0271725", "names": ["Exogenous Cushing Syndrome", "Iatrogenic Cushing disease", "Iatrogenic Cushing Syndrome", "Iatrogenic Cushing's disease", "Iatrogenic Cushing's syndrome", "iatrogenic Cushing's syndrome", "Cushing's syndrome, iatrogenic", "Drug-induced Cushing's syndrome", "Iatrogenic hyperadrenocorticism", "Hyperadrenocorticism, iatrogenic", "Iatrogenic syndrome of excess cortisol", "Iatrogenic Cushing's disease (disorder)", "Cushing; syndrome or disease, iatrogenic", "iatrogenic Cushing's syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Iatrogenic Cushing's disease", "shortest_name_length": 26}
{"curie": "MONDO:0001729", "names": ["cochlear active Mnire's disease", "Active cochlear Ménière disease", "Cochlear active Mnire's disease", "active cochlear Meniere disease", "Active cochlear Meniere's disease", "active cochlear Meniere's disease", "Active cochlear Ménière's disease", "Cochlear active Meniere's disease", "active Meniere's disease, cochlear", "Active Meniere's disease, cochlear", "Active Ménière's disease, cochlear", "Active cochlear Ménière's disease (disorder)", "active cochlear Meniere's disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "active cochlear Meniere disease", "shortest_name_length": 31}
{"curie": "MONDO:0018647", "names": ["Secondary sclerosing cholangitis", "secondary sclerosing cholangitis", "Secondary sclerosing cholangitis (disorder)", "secondary sclerosing cholangitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary sclerosing cholangitis", "shortest_name_length": 32}
{"curie": "UMLS:C5420152", "names": ["Refractory Uveal Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Uveal Melanoma", "shortest_name_length": 25}
{"curie": "MONDO:0021244", "names": ["Submandibular Gland Tumor", "gland submandibular tumor", "submandibular gland tumor", "submandibular gland tumour", "gland submandibular tumors", "tumor of submandibular gland", "Tumor of submandibular gland", "Submandibular Gland Neoplasm", "submandibular gland neoplasm", "Tumor of Submandibular Gland", "Tumour of submandibular gland", "Neoplasm, Submandibular Gland", "Submandibular Gland Neoplasms", "Gland Neoplasm, Submandibular", "Gland Neoplasms, Submandibular", "Neoplasms, Submandibular Gland", "Neoplasm of Submandibular Gland", "neoplasm of submandibular gland", "tumor of the submandibular gland", "Tumor of the Submandibular Gland", "neoplasm of the submandibular gland", "Neoplasm of the Submandibular Gland", "submandibular gland neoplasm (disease)", "neoplasm of submandibular gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "submandibular gland neoplasm", "shortest_name_length": 25}
{"curie": "UMLS:C4525303", "names": ["Stage IIIA Gallbladder Cancer", "Stage IIIA Gallbladder Cancer AJCC v8", "Stage IIIA Gallbladder Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Gallbladder Cancer AJCC v8", "shortest_name_length": 29}
{"curie": "MONDO:0001661", "names": ["diabetic retinopathy background", "Background diabetic retinopathy", "background diabetic retinopathy", "Background Diabetic Retinopathy", "Nonproliferative diabetic retinopathy", "nonproliferative diabetic retinopathy", "BDR - Background diabetic retinopathy", "Non-Proliferative Diabetic Retinopathy", "non proliferative diabetic retinopathy", "Non-proliferative diabetic retinopathy", "non-proliferative diabetic retinopathy", "Non proliferative diabetic retinopathy", "Nonproliferative diabetic retinopathy NOS", "Background diabetic retinopathy (diagnosis)", "NPDR - Non proliferative diabetic retinopathy", "Non-visually threatening diabetic retinopathy", "diabetes with nonproliferative diabetic retinopathy", "Nonproliferative retinopathy due to diabetes mellitus", "diabetes mellitus with nonproliferative diabetic retinopathy", "diabetes with nonproliferative diabetic retinopathy (diagnosis)", "Nonproliferative retinopathy due to diabetes mellitus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "background diabetic retinopathy", "shortest_name_length": 31}
{"curie": "MONDO:0015149", "names": ["Pure SPG", "Pure HSP", "Uncomplicated HSP", "uncomplicated SPG", "uncomplicated HSP", "Uncomplicated SPG", "Pure familial spastic paraplegia", "Pure hereditary spastic paraplegia", "pure hereditary spastic paraplegia", "uncomplicated familial spastic paraplegia", "Uncomplicated familial spastic paraplegia", "Uncomplicated hereditary spastic paraplegia", "uncomplicated hereditary spastic paraplegia", "Pure hereditary spastic paraplegia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pure hereditary spastic paraplegia", "shortest_name_length": 8}
{"curie": "MONDO:0015207", "names": ["isolated esophageal malformation", "nonsyndromic esophageal malformation", "non-syndromic esophageal malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-syndromic esophageal malformation", "shortest_name_length": 32}
{"curie": "MONDO:0003030", "names": ["cervical endometrial stromal sarcoma", "endometrial stromal sarcoma of the cervix", "Endometrioid Stromal Sarcoma of the Cervix", "endometrioid stromal sarcoma of the cervix", "uterine cervix endometrioid stromal sarcoma", "endometrioid stromal sarcoma of uterine cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometrioid stromal sarcoma of the cervix", "shortest_name_length": 36}
{"curie": "MONDO:0011268", "names": ["RTADR", "DRTA3", "type 1 RTA", "classical distal RTA", "type 1 renal tubular acidosis", "RTA, distal, autosomal recessive", "classical distal renal tubular acidosis", "renal tubular acidosis, distal, autosomal recessive", "renal tubular acidosis, autosomal recessive with preserved hearing", "renal tubular acidosis, autosomal recessive, with preserved hearing", "distal renal tubular acidosis 3, with or without sensorineural hearing loss", "renal tubular acidosis, distal, 3, with or without sensorineural hearing loss", "RENAL TUBULAR ACIDOSIS, DISTAL, 3, WITH OR WITHOUT SENSORINEURAL HEARING LOSS", "renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss", "renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss, included"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal tubular acidosis, distal, 3, with or without sensorineural hearing loss", "shortest_name_length": 5}
{"curie": "UMLS:C4553848", "names": ["IVA", "Stage IVA Bladder Cancer", "stage IVA bladder cancer", "Stage IVA Bladder Cancer AJCC v8", "stage IVA bladder cancer AJCC v8", "stage IVA bladder carcinoma AJCC v8", "Stage IVA Bladder Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Bladder Cancer AJCC v8", "shortest_name_length": 3}
{"curie": "MONDO:0013593", "names": ["DFNA64", "autosomal dominant deafness 64", "deafness, autosomal dominant 64", "DEAFNESS, AUTOSOMAL DOMINANT 64", "deafness, autosomal dominant type 64", "autosomal dominant nonsyndromic deafness 64", "DIABLO autosomal dominant nonsyndromic deafness", "autosomal dominant nonsyndromic hearing loss 64", "autosomal dominant nonsyndromic deafness type 64", "autosomal dominant nonsyndromic deafness caused by mutation in DIABLO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 64", "shortest_name_length": 6}
{"curie": "MONDO:0008855", "names": ["BLS", "BLSII", "BLS 2", "BLS Type II", "Bls, type 2", "BLS type II", "BLS, type II", "BLS, TYPE II", "MHC Class II Deficiency", "MHC class II deficiency", "Bare lymphocyte syndrome", "Bare Lymphocyte Syndrome", "BARE LYMPHOCYTE SYNDROME", "bare lymphocyte syndrome", "BARE lymphocyte syndrome", "HLA class 2-negative SCID", "syndrome; bare lymphocyte", "Lymphocyte Syndrome, Bare", "Bare Lymphocyte Syndromes", "Syndrome, Bare Lymphocyte", "Bare lymphocyte syndrome 2", "Syndromes, Bare Lymphocyte", "SCID, HLA Class 2-negative", "SCID, HLA Class 2-Negative", "bare; lymphocyte, syndrome", "Lymphocyte Syndromes, Bare", "SCID, HLA Class II-Negative", "SCID, HLA CLASS II-NEGATIVE", "SCID, HLA Class II-negative", "BLS - Bare lymphocyte syndrome", "Bare lymphocyte syndrome type 2", "Bare Lymphocyte Syndrome Type 2", "bare lymphocyte syndrome type II", "Bare lymphocyte syndrome, type 2", "Bare Lymphocyte Syndrome, Type II", "Bare lymphocyte syndrome, type II", "BARE lymphocyte syndrome, type II", "BARE LYMPHOCYTE SYNDROME, TYPE II", "MHC class II expression deficiency", "bare lymphocyte syndrome (diagnosis)", "SCID due to absent class II HLA antigens", "bare lymphocyte syndrome type II (diagnosis)", "MHC class II deficiency, complementation group B", "HLA class 2-negative severe combined immunodeficiency", "immunodeficiency by defective expression of HLA class 2", "Severe combined immunodeficiency, HLA class ii-negative", "SEVERE COMBINED IMMUNODEFICIENCY, HLA CLASS II-NEGATIVE", "severe combined immunodeficiency, HLA Class II-negative", "severe combined immunodeficiency, HLA class ii-negative", "Immunodeficiency by Defective Expression of MHC Class II", "Immunodeficiency by defective expression of MHC class II", "Bare Lymphocyte Syndrome, Type II, Complementation Group C", "BARE LYMPHOCYTE SYNDROME, TYPE II, COMPLEMENTATION GROUP C", "Bare Lymphocyte Syndrome, Type II, Complementation Group D", "Bare Lymphocyte Syndrome, Type II, Complementation Group E", "Bare lymphocyte syndrome, type II, complementation group B", "BARE LYMPHOCYTE SYNDROME, TYPE II, COMPLEMENTATION GROUP D", "BARE LYMPHOCYTE SYNDROME, TYPE II, COMPLEMENTATION GROUP B", "Bare lymphocyte syndrome, type II, complementation group A", "BARE LYMPHOCYTE SYNDROME, TYPE II, COMPLEMENTATION GROUP E", "Bare lymphocyte syndrome, type II, complementation group D", "Bare lymphocyte syndrome, type II, complementation group E", "Bare lymphocyte syndrome, type II, complementation group C", "Bare Lymphocyte Syndrome, Type II, Complementation Group B", "Bare Lymphocyte Syndrome, Type II, Complementation Group A", "BARE LYMPHOCYTE SYNDROME, TYPE II, COMPLEMENTATION GROUP A", "immunodeficiency by defective expression of HLA class type 2", "major histocompatibility complex class II expression deficiency", "BARE lymphocyte syndrome, type II, complementation group E, included", "BARE lymphocyte syndrome, type II, complementation group C, included", "BARE lymphocyte syndrome, type II, complementation group D, included", "BARE lymphocyte syndrome, type II, complementation group B, included", "Severe combined immunodeficiency (SCID) due to absent class II HLA antigens", "Severe combined immunodeficiency due to absent class II human leukocyte antigens", "severe combined immunodeficiency due to absent class ii human leukocyte antigens", "Severe combined immunodeficiency due to absent class II human leukocyte antigens (disorder)", "severe combined immunodeficiency due to absent class ii human leukocyte antigens (diagnosis)", "SCID, HLA CLASS II-NEGATIVE BARE lymphocyte syndrome, type II, complementation group A, included"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MHC class II deficiency", "shortest_name_length": 3}
{"curie": "UMLS:C0856012", "names": ["MALT Type Extranodal Marginal Zone B-Cell Lymphoma Stage I", "Extranodal marginal zone B-cell lymphoma (MALT type) stage I", "Extranodal Marginal Zone B-Cell Lymphoma (MALT Type) Stage I", "Stage I Extranodal Marginal Zone B-Cell Lymphoma (MALT Type )", "Stage I Extranodal Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue", "Stage I Extranodal Marginal Zone B-Cell Lymphoma of Mucosa-Associated Lymphoid Tissue", "Ann Arbor Stage I Extranodal Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extranodal marginal zone B-cell lymphoma (MALT type) stage I", "shortest_name_length": 58}
{"curie": "UMLS:C1266145", "names": ["Sialoblastoma", "Salivary Gland Sialoblastoma", "Sialoblastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sialoblastoma", "shortest_name_length": 13}
{"curie": "MONDO:0012687", "names": ["CODA", "familial CODA", "Familial CODA", "Cavitary Optic Disc Anomalies", "Cavitary Optic Disk Anomalies", "cavitary optic DISC anomalies", "CAVITARY OPTIC DISC ANOMALIES", "familial cavitary optic disc anomaly", "Familial cavitary optic disc anomaly", "Familial CODA (cavitary optic disc anomaly)", "Familial cavitary optic disc anomaly (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial cavitary optic disc anomaly", "shortest_name_length": 4}
{"curie": "MONDO:0005141", "names": ["Pseudomonas", "infection pseudomona", "Pseudomonas diseases", "Pseudomonas Infection", "Pseudomonas infection", "infection pseudomonas", "pseudomonas infection", "infections pseudomona", "PSEUDOMONAS INFECTION", "Pseudomonas infections", "infections pseudomonas", "Pseudomonal infections", "Pseudomonas Infections", "infection; Pseudomonas", "pseudomonas infections", "Pseudomonas; infection", "Infection, Pseudomonas", "Infections, Pseudomonas", "Pseudomonas infection NOS", "Pseudomonas infectious disease", "Pseudomonas disease or disorder", "Pseudomonas infection (diagnosis)", "Pseudomonas caused disease or disorder", "Bacterial infection due to Pseudomonas", "Bacterial infection caused by Pseudomonas", "Bacterial infection caused by Pseudomonas (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pseudomonas infection", "shortest_name_length": 11}
{"curie": "MONDO:0016013", "names": ["Minamata disease", "Neurologic Mercurialism", "Mercurialism, Neurologic", "Nervous System Mercurialism", "Mercurialism, Nervous System", "Neurologic Mercury Poisoning", "System Mercurialism, Nervous", "Fetal methylmercury syndrome", "fetal methylmercury syndrome", "Poisoning, Neurologic Mercury", "Mercury Poisoning, Neurologic", "Fetal methyl mercury syndrome", "Foetal methylmercury syndrome", "Foetal methyl mercury syndrome", "Mercury neurotoxicity syndrome", "Mercury Neurotoxicity Syndrome", "Poisoning, Mercury, Neurologic", "Syndrome, Mercury Neurotoxicity", "Neurotoxicity Syndrome, Mercury", "Mercury Neurotoxicity Syndromes", "Neurotoxicity Syndromes, Mercury", "Syndromes, Mercury Neurotoxicity", "Methyl mercury antenatal exposure", "Mercury Poisoning, Nervous System", "Nervous System Poisoning, Mercury", "Poisoning, Mercury, Nervous System", "Methyl mercury antenatal infection", "Mercury Induced Nervous System Diseases", "Mercury-Induced Nervous System Diseases", "Fetal methyl mercury syndrome (disorder)", "Nervous System Diseases, Mercury-Induced", "Nervous System Diseases, Mercury Induced"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fetal methylmercury syndrome", "shortest_name_length": 16}
{"curie": "UMLS:C3899007", "names": ["GBS Infection, Early-Onset", "Group B Streptococcal Infection, Early-Onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Group B Streptococcal Infection, Early-Onset", "shortest_name_length": 26}
{"curie": "MONDO:0001564", "names": ["Binocular vision defect", "binocular vision disease", "Binocular vision disorder", "Binocular Vision Disorder", "binocular vision disorder", "binocular; disorder vision", "Binocular vision disorders", "vision; disorder, binocular", "disorder; binocular, vision", "Binocular vision disorder, NOS", "Binocular vision disorder (disorder)", "binocular vision disorder (diagnosis)", "Binocular vision disorder, unspecified", "Unspecified disorder of binocular vision", "simultaneous visual perception without fusion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "binocular vision disease", "shortest_name_length": 23}
{"curie": "UMLS:C1334993", "names": ["Non-Neoplastic Adrenal Gland Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Adrenal Gland Disorder", "shortest_name_length": 37}
{"curie": "MONDO:0021050", "names": ["Vagina Tumor", "vagina tumor", "Vaginal tumor", "vaginal tumor", "tumors vagina", "Vaginal Tumor", "Vaginal tumour", "Tumor of vagina", "Tumor of Vagina", "vagina neoplasm", "Vagina Neoplasm", "tumor of vagina", "Vagina Neoplasms", "Neoplasm, Vagina", "Tumour of vagina", "vaginal neoplasm", "Vaginal neoplasm", "Vaginal Neoplasm", "Neoplasms, Vagina", "Vaginal neoplasia", "VAGINAL NEOPLASIA", "vaginal neoplasms", "Vaginal Neoplasms", "Neoplasm, Vaginal", "Neoplasm of Vagina", "Neoplasm of vagina", "Neoplasms, Vaginal", "neoplasm of vagina", "tumor of the vagina", "Tumor of the Vagina", "Vaginal neoplasm NOS", "neoplasm of the vagina", "Neoplasm of the Vagina", "vagina neoplasm (disease)", "Neoplasm of vagina (disorder)", "neoplasm of vagina (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vaginal neoplasm", "shortest_name_length": 12}
{"curie": "MONDO:0017985", "names": ["radioulnar fusion", "Fused forearm bones", "synostosis radioulnar", "Radioulnar Synostosis", "Radioulnar synostosis", "radioulnar synostosis", "synostosis; radioulnar", "radioulnar; synostosis", "radio-ulnar synostosis", "radial-ulnar synostosis", "radio-ulnar synostosis type 1", "radioulnar synostosis (disease)", "congenital radioulnar synostosis", "Radioulnar synostosis (disorder)", "radioulnar synostosis (diagnosis)", "proximal, smooth fusion of 2-6 CM between the radius and ulna and absent head of the radius"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital radioulnar synostosis", "shortest_name_length": 17}
{"curie": "MONDO:0001320", "names": ["Ring staphyloma", "ring staphyloma", "Ring staphyloma (disorder)", "ring staphyloma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ring staphyloma", "shortest_name_length": 15}
{"curie": "UMLS:C5238478", "names": ["Spiradenocylindrocarcinoma", "Malignant Spiradenocylindroma", "Carcinoma ex Spiradenocylindroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spiradenocylindrocarcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0006571", "names": ["Pinkus", "Lichen nitidus", "lichen nitidus", "Lichen Nitidus", "nitidus; lichen", "lichen; nitidus", "Pinkus' disease", "Lichen nitidus (disorder)", "lichen nitidus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lichen nitidus", "shortest_name_length": 6}
{"curie": "UMLS:C4721654", "names": ["Stage II Ovarian Dysgerminoma", "Stage II Ovarian Dysgerminoma AJCC v7", "Stage II Ovarian Dysgerminoma AJCC v6", "Stage II Ovarian Dysgerminoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Ovarian Dysgerminoma AJCC v6 and v7", "shortest_name_length": 29}
{"curie": "MONDO:0018980", "names": ["Kennedy-Teebi syndrome", "Kennedy Teebi syndrome", "Acrofacial dysostosis Kennedy Teebi type", "acrofacial dysostosis, Kennedy-Teebi type", "Acrofacial dysostosis, Kennedy-Teebi type", "Acrofacial dysostosis Kennedy Teebi type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acrofacial dysostosis, Kennedy-Teebi type", "shortest_name_length": 22}
{"curie": "MONDO:0032775", "names": ["NEDSSWI", "NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND SPEECH AND WALKING IMPAIRMENT", "neurodevelopmental disorder with seizures and speech and walking impairment"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with seizures and speech and walking impairment", "shortest_name_length": 7}
{"curie": "MONDO:0009710", "names": ["THD", "Thomsen Disease", "thomsen disease", "THOMSEN DISEASE", "thomsens disease", "Thomsens Disease", "Disease, Thomsen", "thomsen's disease", "Thomsen's Disease", "ATAXIA MUSCULARIS", "Disease, Thomsens", "Thomsen's disease", "MYOTONIA CONGENITA", "Disease, Thomsen's", "Myotonia Congenita", "myotonia congenita", "Myotonia congenita", "Congenital myotonia", "myotonia; congenita", "Myotonia congenital", "congenital myotonia", "congenita; myotonia", "Congenital Myotonia", "Myopathy, Congenital", "myopathy, congenital", "Generalized Myotonia", "MYOTONIA HEREDITARIA", "Myotonia, Generalized", "Generalized Myotonias", "Myotonias, Generalized", "Congenital myotonia, NOS", "Thomsen and Becker disease", "Thomsen myotonia congenita", "Thomsen Generalized Myotonia", "Myotonia congenita (disorder)", "Generalized Myotonia of Thomsen", "congenital myotonia (diagnosis)", "BATTEN-TURNER CONGENITAL MYOPATHY", "Batten-Turner Congenital Myopathy", "Batten-Turner congenital myopathy", "Batten Turner Congenital Myopathy", "Batten Turner congenital myopathy", "Myotonia Congenita, Autosomal Dominant", "MYOTONIA CONGENITA, AUTOSOMAL DOMINANT", "Congenital myotonia, autosomal dominant form", "Myotonia congenita - autosomal dominant form", "Dominant myotonia congenita [Thomsen disease]", "Congenital myotonia, autosomal dominant form (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thomsen and Becker disease", "shortest_name_length": 3}
{"curie": "UMLS:C0852722", "names": ["Postcricoid Cancer", "Postcricoid cancer", "Postcricoid Carcinoma", "Postcricoid Throat Cancer", "Cancer of Postcricoid Area", "Cancer of the Postcricoid Area"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postcricoid cancer", "shortest_name_length": 18}
{"curie": "UMLS:C0240396", "names": ["Mucous Membrane Leukoplakia", "MUCOUS MEMBRANE LEUKOPLAKIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mucous Membrane Leukoplakia", "shortest_name_length": 27}
{"curie": "MONDO:0009374", "names": ["Hydroxyprolinemia", "hydroxyprolinemia", "HYDROXYPROLINEMIA", "hydroxyprolinaemia", "Hydroxyprolinaemia", "hyperhydroxyprolinemia", "Hyperhydroxyprolinemia", "Hyperhydroxyprolinaemia", "hydroxyprolinemia (disease)", "hydroxyprolinemia (diagnosis)", "High blood hydroxyproline levels", "Hyperhydroxyprolinemia (disorder)", "4-HYDROXY-L-PROLINE OXIDASE DEFICIENCY", "4-hydroxy-L-proline oxidase deficiency", "4-Hydroxy-L-Proline Oxidase Deficiency", "4 alpha hydroxy-L-proline oxidase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hydroxyprolinemia", "shortest_name_length": 17}
{"curie": "MONDO:0015239", "names": ["a.pulmonalis; anomaly (origin)", "anomaly; pulmonary artery (origin)", "Pulmonary artery, anomalous origin", "Abnormal origin of pulmonary artery", "Anomalous origin of pulmonary artery", "Abnormal origin of the pulmonary artery", "abnormal origin of the pulmonary artery", "Anomalous origin of pulmonary artery (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "abnormal origin of the pulmonary artery", "shortest_name_length": 30}
{"curie": "UMLS:C5237234", "names": ["Cisplatin-Induced Tinnitus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cisplatin-Induced Tinnitus", "shortest_name_length": 26}
{"curie": "UMLS:C0272576", "names": ["PELVIS FRACTURE CLOSED", "closed pelvic fracture", "closed fracture of pelvis", "Closed Fracture of Pelvis", "Closed fracture of pelvis", "Closed fracture of pelvis, NOS", "Closed fracture of pelvis (disorder)", "Unspecified closed fracture of pelvis", "Closed unspecified fracture of pelvis", "closed fracture of pelvis (diagnosis)", "Fracture of pelvis, unspecified, closed"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Closed fracture of pelvis", "shortest_name_length": 22}
{"curie": "UMLS:C0349526", "names": ["Benign tumor of fibrous tissue", "Benign tumour of fibrous tissue", "Benign Fibrous Tissue Skin Tumor", "Benign Cutaneous Fibrous Neoplasm", "Benign Skin Fibroblastic Neoplasm", "Benign Fibrous Tissue Skin Neoplasm", "Benign Cutaneous Fibroblastic Tumor", "Benign Fibrous Tissue Tumor of Skin", "Benign Cutaneous Fibrocytic Neoplasm", "Benign Cutaneous Fibroblastic Neoplasm", "Benign Fibrous Tissue Neoplasm of Skin", "Benign Cutaneous Fibrous Tissue Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Skin Fibroblastic Neoplasm", "shortest_name_length": 30}
{"curie": "MONDO:0005603", "names": ["pancreas tubular adenocarcinoma", "pancreatic tubular adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic tubular adenocarcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0015387", "names": ["dacryocele", "dacryocystocele", "nasolacrimal mucocele", "nasolacrimal duct cyst"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasolacrimal duct cyst", "shortest_name_length": 10}
{"curie": "MONDO:0043555", "names": ["diarrhea infant", "infant diarrhea", "toddler diarrhea", "diarrhea toddler", "diarrhea infants", "Toddler diarrhea", "diarrhoea infant", "Diarrhoea;infant", "infant diarrhoea", "diarrhea toddlers", "toddler diarrhoea", "Toddler diarrhoea", "diarrhoea infants", "Infantile Diarrhea", "diarrhoea toddlers", "diarrhea infantile", "Infantile diarrhea", "infantile diarrhea", "Infantile diarrhoea", "Infantile Diarrheas", "Diarrhea, Infantile", "infantile Diarrheas", "Diarrheas, infantile", "Diarrheas, Infantile", "Summer diarrhea of infants", "infantile diarrheal disease", "Toddler diarrhea (disorder)", "Summer diarrhoea of infants", "Toddler diarrhea (diagnosis)", "diarrheal disease of infancy", "infantile onset diarrheal disease", "intestinal disorder diarrheal toddler"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile diarrhea", "shortest_name_length": 15}
{"curie": "MONDO:0008568", "names": ["defect", "DEFECT", "Thyroid hormone plasma membrane transport defect", "THYROID HORMONE PLASMA MEMBRANE TRANSPORT DEFECT", "thyroid hormone plasma membrane transport defect", "hyperthyroxinemia, Eumetabolic, due to T4 plasma Membrane Transport", "Hyperthyroxinemia, eumetabolic, due to T4 plasma membrane transport", "HYPERTHYROXINEMIA, EUMETABOLIC, DUE TO T4 PLASMA MEMBRANE TRANSPORT", "THYROID HORMONE RESISTANCE DUE TO T4 PLASMA MEMBRANE TRANSPORT DEFECT", "thyroid hormone resistance due to T4 plasma Membrane Transport defect", "Thyroid hormone resistance due to T4 plasma membrane transport defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid hormone plasma membrane transport defect", "shortest_name_length": 6}
{"curie": "MONDO:0007013", "names": ["Vasculogenic Impotence", "vasculogenic impotence", "Impotence, Vasculogenic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vasculogenic impotence", "shortest_name_length": 22}
{"curie": "UMLS:C0349735", "names": ["infection ovary", "ovary infection", "ovary; infection", "infections ovary", "infection; ovary", "infection ovarian", "ovarian infection", "Ovarian Infection", "infection ovaries", "OVARIAN INFECTION", "Ovarian infection", "infections ovarian", "Infection of ovary", "infections ovaries", "infection of ovary", "Ovarian infection (diagnosis)", "Infection of ovary (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Infection", "shortest_name_length": 15}
{"curie": "MONDO:0006643", "names": ["alcohol; cardiomyopathy", "cardiomyopathy; alcohol", "Alcoholic cardiomyopathy", "alcoholic cardiomyopathy", "CARDIOMYOPATHY ALCOHOLIC", "Cardiomyopathy alcoholic", "Alcoholic Cardiomyopathy", "CARDIOMYOPATHY, ALCOHOLIC", "Cardiomyopathy, Alcoholic", "cardiomyopathy; alcoholic", "alcoholic heart muscle disease", "alcohol-induced heart muscle disease", "Alcohol-induced heart muscle disease", "Alcohol induced heart muscle disease", "alcoholic cardiomyopathy (diagnosis)", "Dilated cardiomyopathy caused by alcohol", "Dilated cardiomyopathy caused by ethanol", "Dilated cardiomyopathy secondary to alcohol", "dilated cardiomyopathy secondary to alcohol", "Dilated cardiomyopathy caused by ethanol (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alcoholic cardiomyopathy", "shortest_name_length": 23}
{"curie": "UMLS:C0855261", "names": ["Erotomanic Type Delusional Disorder", "Delusional disorder, erotomanic type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Delusional disorder, erotomanic type", "shortest_name_length": 35}
{"curie": "UMLS:C4524717", "names": ["Clinical Stage IV Gastroesophageal Junction Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage IV Gastroesophageal Junction Adenocarcinoma AJCC v8", "shortest_name_length": 66}
{"curie": "UMLS:C0280734", "names": ["aids-related cancer", "AIDS-Related Cancer", "AIDS-related cancer", "AIDS Related Cancer", "AIDS related cancer", "cancer, AIDS related", "AIDS related cancers", "AIDS-associated cancer", "AIDS-Related Malignancy", "AIDS-Related Malignancies", "aids-related malignancies", "AIDS related malignancies", "AIDS-related malignancies", "malignancies, AIDS-related", "AIDS-Related Malignant Neoplasm", "HIV-Associated Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Malignant Neoplasm", "shortest_name_length": 19}
{"curie": "DOID:0080832", "names": ["mild cognitive impairment"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mild cognitive impairment", "shortest_name_length": 25}
{"curie": "UMLS:C1142379", "names": ["Neurotmeses", "Neurotmesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neurotmesis", "shortest_name_length": 11}
{"curie": "MONDO:0024325", "names": ["Glomangiomyoma of skin", "glomangiomyoma of skin", "cutaneous glomangiomyoma", "zone of skin glomangiomyoma", "Glomangiomyoma of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous glomangiomyoma", "shortest_name_length": 22}
{"curie": "MONDO:0035405", "names": ["seromucinous cystadenoma of childhood", "Seromucinous cystadenoma of ovary in childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "seromucinous cystadenoma of childhood", "shortest_name_length": 37}
{"curie": "UMLS:C3828416", "names": ["Radiation Damage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radiation Damage", "shortest_name_length": 16}
{"curie": "MONDO:0021280", "names": ["parotid mucoepidermoid carcinoma", "Parotid Mucoepidermoid Carcinoma", "Mucoepidermoid Carcinoma of Parotid", "mucoepidermoid carcinoma of parotid", "parotid gland mucoepidermoid carcinoma", "Parotid Gland Mucoepidermoid Carcinoma", "mucoepidermoid carcinoma of the parotid", "Mucoepidermoid Carcinoma of the Parotid", "Cancer of parotid gland, mucoepidermoid", "Mucoepidermoid Carcinoma of Parotid Gland", "mucoepidermoid carcinoma of parotid gland", "Mucoepidermoid carcinoma of parotid gland", "mucoepidermoid carcinoma of the parotid gland", "Mucoepidermoid Carcinoma of the Parotid Gland", "Mucoepidermoid carcinoma of parotid gland (disorder)", "mucoepidermoid carcinoma of parotid gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucoepidermoid carcinoma of parotid gland", "shortest_name_length": 32}
{"curie": "UMLS:C0241616", "names": ["vagina atrophy", "Vaginal Atrophy", "Atrophy;vaginal", "VAGINAL ATROPHY", "atrophy; vagina", "vagina; atrophy", "vaginal atrophy", "Atrophy of vagina", "Atrophy of vagina (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atrophy of vagina", "shortest_name_length": 14}
{"curie": "UMLS:C0278860", "names": ["Anaplastic Small Cell Thyroid Carcinoma", "Anaplastic Small Cell Carcinoma of Thyroid", "Anaplastic Small Cell Thyroid Gland Carcinoma", "Undifferentiated Small Cell Thyroid Carcinoma", "Anaplastic Small Cell Carcinoma of the Thyroid", "Undifferentiated Small Cell Carcinoma of Thyroid", "Anaplastic Small Cell Carcinoma of Thyroid Gland", "Thyroid Gland Undifferentiated Small Cell Carcinoma", "Undifferentiated Small Cell Thyroid Gland Carcinoma", "Undifferentiated Small Cell Carcinoma of the Thyroid", "Anaplastic Small Cell Carcinoma of the Thyroid Gland", "Undifferentiated Small Cell Carcinoma of Thyroid Gland", "Undifferentiated Small Cell Carcinoma of the Thyroid Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anaplastic Small Cell Thyroid Carcinoma", "shortest_name_length": 39}
{"curie": "UMLS:C0269131", "names": ["Female genital fistula", "female genital fistula", "female fistula genital", "Fistula;genital tract;F", "female genital tract fistula", "Female Genital Tract Fistula", "Female genital tract fistula", "Female genital tract fistula NOS", "Fistula of the female genital tract", "Fistula of the female genital organs", "FISTULAS OF THE FEMALE GENITAL ORGANS", "Fistula of the female genital tract, NOS", "Female genital tract fistula, unspecified", "Fistula of the female genital organs, NOS", "Fistula of the female genital organs (disorder)", "Unspecified fistula involving female genital tract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fistula of the female genital organs", "shortest_name_length": 22}
{"curie": "UMLS:C0024118", "names": ["Parasitic Lung Disease", "Lung Disease, Parasitic", "Parasitic Lung Diseases", "Lung Parasitic Infection", "Lung Diseases, Parasitic", "Parasitic lung infection", "Lung Parasitic Infections", "Parasitic infection of lung", "Parasitic Infections of Lung", "Pulmonary Parasitic Infection", "Pulmonary Parasitic Infections", "Parasitic Infection, Pulmonary", "Parasitic Infections, Pulmonary", "Parasitic infection of lung (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Diseases, Parasitic", "shortest_name_length": 22}
{"curie": "UMLS:C1710126", "names": ["Solitary Osteochondroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Solitary Osteochondroma", "shortest_name_length": 23}
{"curie": "UMLS:C5670668", "names": ["Stage I Cervical Cancer FIGO 2009", "Stage I Cervical Carcinoma FIGO 2009"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Cervical Cancer FIGO 2009", "shortest_name_length": 33}
{"curie": "UMLS:C0032268", "names": ["Airocele", "Airocoele", "Pneumocranium", "Pneumocephalus", "pneumocephalus", "Intracranial Gas", "Cranial Airocele", "Airocele, Cranial", "Gas, Intracranial", "Cranial Airoceles", "Airoceles, Cranial", "Cranial Pneumocyst", "Cranial Pneumocysts", "Pneumocyst, Cranial", "Pneumocysts, Cranial", "Pneumocephalus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pneumocephalus", "shortest_name_length": 8}
{"curie": "UMLS:C4521642", "names": ["Stage III Esophageal Adenocarcinoma", "Clinical Stage III Esophageal Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage III Esophageal Adenocarcinoma AJCC v8", "shortest_name_length": 35}
{"curie": "EFO:0009855", "names": ["frontal fibrosing alopecia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontal fibrosing alopecia", "shortest_name_length": 26}
{"curie": "UMLS:C1335357", "names": ["Parotid Gland Carcinosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parotid Gland Carcinosarcoma", "shortest_name_length": 28}
{"curie": "MONDO:0010929", "names": ["CRS4", "CRANIOSYNOSTOSIS 4", "craniosynostosis 4", "ERF craniosynostosis", "craniosynostosis type 4", "ERF-related craniosynostosis", "craniosynostosis caused by mutation in ERF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniosynostosis 4", "shortest_name_length": 4}
{"curie": "MONDO:0010854", "names": ["OES", "oes", "OCULOECTODERMAL SYNDROME", "Oculoectodermal Syndrome", "oculoectodermal syndrome", "Oculoectodermal syndrome", "oculo-ectodermal syndrome", "Toriello-Lacassie-Droste syndrome", "oculoectodermal syndrome, somatic", "Toriello Lacassie Droste syndrome", "Aplasia Cutis Congenita with Epibulbar Dermoids", "APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS", "aplasia cutis congenita with epibulbar dermoids", "aplasia cutis congenita-epibulbar dermoids syndrome", "Aplasia cutis congenita-epibulbar dermoids syndrome", "Aplasia cutis congenita with epibulbar dermoid syndrome", "Aplasia cutis congenita with epibulbar dermoid syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Toriello-Lacassie-Droste syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C2981403", "names": ["Stage IIIC Colorectal Cancer", "Stage IIIC Colorectal Cancer AJCC v7", "Stage IIIC Colorectal (Colon or Rectal) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Colorectal Cancer AJCC v7", "shortest_name_length": 28}
{"curie": "MONDO:0012805", "names": ["ped", "PED", "DYT18", "GLUT1DS2", "DYT-SLC2A1", "PxMD-SLC2A1", "DYSTONIA 18", "Dystonia 18", "dystonia 18", "GLUT1 deficiency syndrome 2", "GLUT1 DEFICIENCY SYNDROME 2", "GLUT1 deficiency syndrome type 2", "paroxysmal exercise-induced dystonia", "Paroxysmal Exercise-Induced Dystonia", "Paroxysmal dystonia, exercise-induced", "Paroxysmal Exertion-Induced Dyskinesia", "Paroxysmal exertion-induced dyskinesia", "paroxysmal exertion-induced dyskinesia", "childhood onset GLUT1 deficiency syndrome 2", "GLUT1 deficiency syndrome 2, childhood onset", "childhood onset GLUT1 deficiency syndrome type 2", "Paroxysmal exertion-induced dyskinesia (disorder)", "PED WITH OR WITHOUT EPILEPSY AND/OR HEMOLYTIC ANEMIA", "ped with or without epilepsy and/or hemolytic Anemia", "paroxysmal exertion-induced dystonia with or without epilepsy and/or hemolytic Anemia", "PAROXYSMAL EXERTION-INDUCED DYSTONIA WITH OR WITHOUT EPILEPSY AND/OR HEMOLYTIC ANEMIA", "PAROXYSMAL EXERCISE-INDUCED DYSKINESIA WITH OR WITHOUT EPILEPSY AND/OR HEMOLYTIC ANEMIA", "paroxysmal exercise-induced dyskinesia with or without epilepsy and/or hemolytic Anemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood onset GLUT1 deficiency syndrome 2", "shortest_name_length": 3}
{"curie": "MONDO:0014775", "names": ["COXPD28", "combined oxidative phosphorylation deficiency 28", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28", "combined oxidative phosphorylation defect type 28", "Combined oxidative phosphorylation defect type 28", "combined oxidative phosphorylation deficiency type 28", "SLC25A26 combined oxidative phosphorylation deficiency", "COXPD28 - combined oxidative phosphorylation defect type 28", "Combined oxidative phosphorylation defect type 28 (disorder)", "combined oxidative phosphorylation deficiency caused by mutation in SLC25A26", "neonatal severe cardiopulmonary failure due to mitochondrial methylation defect", "Neonatal severe cardiopulmonary failure due to mitochondrial methylation defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation deficiency 28", "shortest_name_length": 7}
{"curie": "UMLS:C3812874", "names": ["EIN", "EmGD", "EAH/EIN", "Endometrial Glandular Dysplasia", "Atypical Endometrial Hyperplasia", "Atypical Hyperplasia of Endometrium", "Endometrial Hyperplasia with Atypia", "endometrial intraepithelial neoplasia", "Endometrial Intraepithelial Neoplasia", "Endometrial intraepithelial neoplasia", "Endometrioid intraepithelial neoplasia", "Atypical Hyperplasia of the Endometrium", "Atypical hyperplasia of the endometrium", "EIN - endometrial intraepithelial neoplasia", "Endometrial intraepithelial neoplasia [EIN]", "Endometrial intraepithelial neoplasia (EIN)", "Endometrial intraepithelial neoplasia (disorder)", "endometrial intraepithelial neoplasia (diagnosis)", "Atypical hyperplasia/Endometrial intraepithelial neoplasia (EIN)", "Endometrioid intraepithelial neoplasia (morphologic abnormality)", "Endometrial Atypical Hyperplasia/Endometrioid Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endometrioid intraepithelial neoplasia", "shortest_name_length": 3}
{"curie": "UMLS:C1336851", "names": ["Umbilical Hernia with Obstruction without Mention of Gangrene"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Umbilical Hernia with Obstruction without Mention of Gangrene", "shortest_name_length": 61}
{"curie": "MONDO:0003876", "names": ["eyelid carcinoma", "Eyelid Carcinoma", "carcinoma of eyelid", "Carcinoma of Eyelid", "Blepharal carcinoma", "Carcinoma of the Eyelid", "carcinoma of the eyelid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eyelid carcinoma", "shortest_name_length": 16}
{"curie": "MONDO:0018355", "names": ["SIM1-related PWLS", "PWS-like due to point mutation", "PWS-like due to a point mutation", "SIM1-related Prader-Willi-like syndrome", "Prader-Willi-like syndrome due to a point mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SIM1-related Prader-Willi-like syndrome", "shortest_name_length": 17}
{"curie": "MONDO:0015804", "names": ["infant botulism", "Infant Botulism", "Infant botulism", "botulism; infant", "infant; botulism", "Botulism, Infant", "Infant Botulisms", "Infantile botulism", "infantile botulism", "Infantile Botulism", "BOTULISM, INFANTILE", "botulism of infancy", "Botulism, Infantile", "infantile onset botulism", "Infant intestinal botulism", "infant intestinal botulism", "infant botulism (diagnosis)", "Infantile botulism (disorder)", "Infant intestinal toxemia botulism", "infant intestinal toxemia botulism", "Infant intestinal toxin-mediated botulism", "infant intestinal toxin-mediated botulism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infant botulism", "shortest_name_length": 15}
{"curie": "UMLS:C2931253", "names": ["Alport syndrome, dominant type", "Renal failure, and sensorineural hearing loss"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alport syndrome, dominant type", "shortest_name_length": 30}
{"curie": "MONDO:0001686", "names": ["Anatomical narrow angle borderline glaucoma", "anatomical narrow angle borderline glaucoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anatomical narrow angle borderline glaucoma", "shortest_name_length": 43}
{"curie": "MONDO:0004457", "names": ["Maxillary Sinus Papilloma", "maxillary sinus Schneiderian papilloma", "Maxillary Sinus Schneiderian Papilloma", "Schneiderian papilloma of maxillary sinus", "Schneiderian Papilloma of Maxillary Sinus", "Schneiderian papilloma of the maxillary sinus", "Schneiderian Papilloma of the Maxillary Sinus", "maxillary sinus paranasal sinus Schneiderian papilloma", "paranasal sinus Schneiderian papilloma of maxillary sinus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maxillary sinus Schneiderian papilloma", "shortest_name_length": 25}
{"curie": "MONDO:0008785", "names": ["SIDBA2", "sideroblastic anemia 2", "pyridoxine refractory sideroblastic anemia", "anemia, sideroblastic, 2, pyridoxine-refractory", "ANEMIA, SIDEROBLASTIC, 2, PYRIDOXINE-REFRACTORY", "pyridoxine-refractory autosomal recessive sideroblastic anemia", "sideroblastic anemia pyridoxine-refractory autosomal recessive", "pyridoxine-refractory autosomal recessive sideroblastic anaemia", "autosomal recessive pyridoxine-refractory sideroblastic anemia 2", "anemia, sideroblastic, pyridoxine-refractory, autosomal recessive", "autosomal recessive pyridoxine-refractory sideroblastic anaemia 2", "Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sideroblastic anemia 2", "shortest_name_length": 6}
{"curie": "MONDO:0025404", "names": ["Bluecomb disease", "Bluecomb of turkeys", "Bluecomb of Turkeys", "Bluecomb disease (disorder)", "Coronaviral enteritis of turkey", "coronaviral enteritis of turkeys", "Transmissible enteritis of turkey", "Transmissible Enteritis of Turkeys", "transmissible enteritis of turkeys", "Enteritis, Transmissible, of Turkeys", "enteritis, transmissible, of turkeys"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coronaviral enteritis of turkeys", "shortest_name_length": 16}
{"curie": "UMLS:C0269802", "names": ["Amnion Nodosum", "amnion nodosum", "Amnion nodosum", "Amnion nodosum (disorder)", "amnion nodosum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Amnion nodosum", "shortest_name_length": 14}
{"curie": "UMLS:C0496956", "names": ["breast neoplasm of uncertain behavior", "neoplasm of uncertain behavior of breast", "Neoplasm of uncertain behavior of breast", "Neoplasm of uncertain behaviour of breast", "Neoplasm of uncertain behavior of breast (disorder)", "Neoplasm of uncertain or unknown behavior of breast", "Neoplasm of uncertain or unknown behaviour of breast", "neoplasm of uncertain behavior of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplasm of uncertain or unknown behavior of breast", "shortest_name_length": 37}
{"curie": "MONDO:0030693", "names": ["IMD96", "IMMUNODEFICIENCY 96", "immunodeficiency 96", "immunodeficiency, autosomal recessive due to LIG1 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 96", "shortest_name_length": 5}
{"curie": "UMLS:C0405107", "names": ["Placenta accreta spectrum", "Morbidly adherent placenta", "morbidly adherent placenta", "Morbidly Adherent Placenta", "Morbidly Adherent Placentation", "MAP - Morbidly adherent placenta", "Morbidly adherent placenta (disorder)", "morbidly adherent placenta (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Morbidly adherent placenta (disorder)", "shortest_name_length": 25}
{"curie": "MONDO:0004293", "names": ["SUPRAGLOTTIC CANCER SQUAMOUS CELL", "Supraglottis Epidermoid Carcinoma", "supraglottic epidermoid carcinoma", "supraglottis epidermoid carcinoma", "Supraglottic Epidermoid Carcinoma", "epidermoid carcinoma of supraglottis", "Supraglottic Squamous Cell Carcinoma", "supraglottis squamous cell carcinoma", "Epidermoid Carcinoma of Supraglottis", "Supraglottis Squamous Cell Carcinoma", "supraglottic squamous cell carcinoma", "squamous cell carcinoma of supraglottis", "Squamous Cell Carcinoma of Supraglottis", "Epidermoid carcinoma of the Supraglottis", "Epidermoid Carcinoma of the Supraglottis", "epidermoid carcinoma of the supraglottis", "squamous cell carcinoma of the supraglottis", "Squamous Cell Carcinoma of the Supraglottis", "supraglottic part of larynx squamous cell carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "supraglottis squamous cell carcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C1336537", "names": ["Supratentorial Meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Supratentorial Meningioma", "shortest_name_length": 25}
{"curie": "MONDO:0002520", "names": ["ALAD deficiency", "acute porphyria", "liver porphyria", "Hepatic porphyria", "Hepatic Porphyria", "hepatic porphyria", "Porphyria hepatic", "Porphyria, Hepatic", "porphyria, hepatic", "Hepatic Porphyrias", "hepatic Porphyrias", "porphyria of liver", "Porphyria, hepatic", "Porphyrias, Hepatic", "Hepatic porphyria, NOS", "acute hepatic porphyria", "Hepatic porphyria (disorder)", "porphobilinogen synthase deficiency", "Delta-aminolevulinate dehydratase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatic porphyria", "shortest_name_length": 15}
{"curie": "MONDO:0700054", "names": ["microcephaly 6 with or without short stature"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly 6 with or without short stature", "shortest_name_length": 44}
{"curie": "MONDO:0020466", "names": ["monosomy X", "Monosomy X", "XO syndrome", "45, X syndrome", "monosomy type X", "Karyotype 45, X", "Monosomy X (disorder)", "XO Gonadal Dysgenesis", "XO - Turner's syndrome", "Gonadal Dysgenesis, XO", "45XO - Turner's syndrome", "Gonadal Dysgenesis, 45,X"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "monosomy X", "shortest_name_length": 10}
{"curie": "UMLS:C5557155", "names": ["Stage IB Cervical Cancer AJCC v9", "Stage IB Cervical Carcinoma AJCC v9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Cervical Cancer AJCC v9", "shortest_name_length": 32}
{"curie": "UMLS:C2697358", "names": ["46,XY TRUE HERMAPHRODITISM", "46,XY True Hermaphroditism", "46,XY Ovotesticular Differences of Sex Development"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XY Ovotesticular Differences of Sex Development", "shortest_name_length": 26}
{"curie": "MONDO:0011188", "names": ["ARVC3", "ARVD3", "arrhythmogenic right ventricular dysplasia 3", "Arrhythmogenic Right Ventricular Cardiomyopathy 3", "arrhythmogenic right ventricular dysplasia type 3", "arrhythmogenic right ventricular cardiomyopathy 3", "ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 3", "familial arrhythmogenic right ventricular dysplasia 3", "arrhythmogenic right ventricular dysplasia, familial, 3", "Arrhythmogenic Right Ventricular Dysplasia, Familial, 3", "ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 3", "ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 3 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arrhythmogenic right ventricular dysplasia 3", "shortest_name_length": 5}
{"curie": "UMLS:C0004032", "names": ["Generalized aspergillosis", "generalized; aspergillosis", "disseminated aspergillosis", "ASPERGILLOSIS DISSEMINATED", "aspergillosis; generalized", "aspergillosis disseminated", "Disseminated aspergillosis", "aspergillosis; disseminated", "disseminated; aspergillosis", "Aspergillosis, disseminated", "Disseminated aspergillosis (disorder)", "disseminated aspergillosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disseminated aspergillosis", "shortest_name_length": 25}
{"curie": "MONDO:0001710", "names": ["Bile Duct Perforation", "Perforation bile duct", "perforation; bile duct", "bile duct; perforation", "Perforation of bile duct", "perforation of bile duct", "d.choledochus; perforation", "Perforation of bile duct (disorder)", "perforation of bile duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "perforation of bile duct", "shortest_name_length": 21}
{"curie": "MONDO:0006059", "names": ["Nasal Cavity Squamous Cell Carcinoma", "nasal cavity squamous cell carcinoma", "Squamous Cell Carcinoma of Nasal Cavity", "squamous cell carcinoma of nasal cavity", "Squamous Cell Carcinoma of the Nasal Cavity", "squamous cell carcinoma of the nasal cavity", "Squamous cell carcinoma of the nasal cavity", "squamous cell carcinoma of nasal cavity (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasal cavity squamous cell carcinoma", "shortest_name_length": 36}
{"curie": "UMLS:C4527060", "names": ["Clinical Stage IIA Merkel Cell Carcinoma AJCC v8", "Clinical Stage IIA Neuroendocrine Carcinoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage IIA Merkel Cell Carcinoma AJCC v8", "shortest_name_length": 48}
{"curie": "UMLS:C3899983", "names": ["BCLC Stage 0 Hepatocellular Cancer", "BCLC Stage 0 Adult Hepatocellular Carcinoma", "Barcelona Clinic Liver Cancer Stage 0 Adult Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "BCLC Stage 0 Adult Hepatocellular Carcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0100083", "names": ["FPDMM", "FPD/AML syndrome", "FPS/AML syndrome", "asprin-like platelet disorder", "platelet disorder, aspirin-like", "familial platelet disorder with associated myeloid malignancy", "platelet disorder, familial, with associated myeloid malignancy", "familial thrombocytopenia with propensity to acute myelogenous leukemia", "thrombocytopenia, familial, with propensity to acute myelogenous leukemia", "familial platelet syndrome with predisposition to acute myelogenous leukemia", "hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1", "shortest_name_length": 5}
{"curie": "UMLS:C3640085", "names": ["Perinatal Aspiration of Blood", "Perinatal Blood Aspiration Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perinatal Blood Aspiration Syndrome", "shortest_name_length": 29}
{"curie": "MONDO:0003550", "names": ["Esophageal Adenosquamous Cancer", "esophageal adenosquamous cancer", "esophagus adenosquamous carcinoma", "esophageal adenosquamous carcinoma", "Esophageal adenosquamous carcinoma", "Esophageal Adenosquamous Carcinoma", "Oesophageal adenosquamous carcinoma", "adenosquamous carcinoma of esophagus", "adenosquamous carcinoma of esophagus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophageal adenosquamous carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0017600", "names": ["HCL-V", "HCL-v", "Hairy cell leukemia variant", "hairy cell leukemia variant", "hairy-cell leukemia variant", "Hairy Cell Leukemia Variant", "Hairy cell leukaemia variant", "hairy cell leukaemia variant", "leukemia hairy-cell - variant", "Prolymphocytic variant of HCL", "prolymphocytic variant of HCL", "Leukemic reticuloendotheliosis variant", "leukemic reticuloendotheliosis variant", "Hairy cell leukemia variant (disorder)", "hairy-cell leukemia variant (diagnosis)", "prolymphocytic variant of hairy cell leukemia", "Prolymphocytic Variant of Hairy Cell Leukemia", "Prolymphocytic variant of hairy cell leukemia", "Hairy cell leukemia variant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hairy cell leukemia variant", "shortest_name_length": 5}
{"curie": "UMLS:C0854833", "names": ["Stage I Angiocentric Lymphoma", "Angiocentric lymphoma stage I", "Angiocentric Lymphoma Stage I", "Nasal T-cell lymphoma stage I", "Polymorphic reticulosis stage I", "Stage I Nasal Type NK/T-Cell Lymphoma", "Ann Arbor Stage I Nasal Type NK/T-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Angiocentric lymphoma stage I", "shortest_name_length": 29}
{"curie": "UMLS:C1266120", "names": ["Malignant Hemangiopericytoma", "Malignant Solitary Fibrous Tumor", "malignant solitary fibrous tumor", "Solitary fibrous tumor, malignant", "malignant solitary fibrous tumor (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Solitary Fibrous Tumor", "shortest_name_length": 28}
{"curie": "UMLS:C5236043", "names": ["Aggressive Prostate Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aggressive Prostate Adenocarcinoma", "shortest_name_length": 34}
{"curie": "UMLS:C4086175", "names": ["Childhood Testicular Non-Seminomatous Germ Cell Tumor", "Childhood Testicular Non-Germinomatous Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Testicular Non-Seminomatous Germ Cell Tumor", "shortest_name_length": 53}
{"curie": "MONDO:0002141", "names": ["PDS", "vaginal melanoma", "Pleomorphic Dermal Sarcoma", "Malignant Skin Fibrous Histiocytoma", "malignant skin fibrous histiocytoma", "Malignant Fibrous Histiocytoma of Skin", "Malignant fibrous histiocytoma of skin", "malignant fibrous histiocytoma of skin", "Malignant Cutaneous Fibrous Histiocytoma", "malignant cutaneous fibrous histiocytoma", "cutaneous malignant fibrous histiocytoma", "Cutaneous Malignant Fibrous Histiocytoma", "Skin Undifferentiated Pleomorphic Sarcoma", "cutaneous unclassified pleomorphic sarcoma", "Malignant Fibrous Histiocytoma of the Skin", "malignant fibrous histiocytoma of the skin", "Cutaneous Unclassified Pleomorphic Sarcoma", "cutaneous undifferentiated pleomorphic sarcoma", "Cutaneous Undifferentiated Pleomorphic Sarcoma", "zone of skin undifferentiated pleomorphic sarcoma", "Malignant fibrous histiocytoma of skin (disorder)", "malignant fibrous histiocytoma of skin (diagnosis)", "undifferentiated pleomorphic sarcoma of zone of skin", "cutaneous unclassified pleomorphic sarcoma (formerly cutaneous)", "Cutaneous Unclassified Pleomorphic Sarcoma (Formerly Cutaneous \"MFH\")", "cutaneous unclassified pleomorphic sarcoma (formerly cutaneous \"MFH\")", "cutaneous unclassified pleomorphic sarcoma (formerly cutaneous \"malignant fibrous histiocytoma\")", "Cutaneous Unclassified Pleomorphic Sarcoma (Formerly Cutaneous \"Malignant Fibrous Histiocytoma\")"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous undifferentiated pleomorphic sarcoma", "shortest_name_length": 3}
{"curie": "MONDO:0018307", "names": ["NBIA", "Neurodegeneration with brain iron accumulation", "neurodegeneration with brain iron accumulation", "Neurodegeneration with brain iron accumulation (NBIA)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodegeneration with brain iron accumulation", "shortest_name_length": 4}
{"curie": "UMLS:C4721579", "names": ["Metastatic colorectal cancer", "metastatic colorectal cancer", "Colorectal cancer metastatic", "Metastasis from malignant neoplasm of colon and/or rectum", "Metastasis from malignant neoplasm of colon and/or rectum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastasis from malignant neoplasm of colon and/or rectum", "shortest_name_length": 28}
{"curie": "MONDO:0007968", "names": ["GP90", "melanoma tumor antigen Gp90", "MELANOMA TUMOR ANTIGEN GP90", "CLASS 1 UNIQUE TUMOR ANTIGEN OF MELANOMA", "Class 1 unique tumor antigen of melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melanoma tumor antigen Gp90", "shortest_name_length": 4}
{"curie": "UMLS:C5555064", "names": ["Low Grade Central Chondrosarcoma", "Low-Grade Central Chondrosarcoma", "Central Atypical Cartilaginous Tumor/Chondrosarcoma, Grade 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Atypical Cartilaginous Tumor/Chondrosarcoma, Grade 1", "shortest_name_length": 32}
{"curie": "MONDO:0019797", "names": ["Acrodysplasia", "acrodysplasia", "acrodysostosis", "Acrodysostosis", "Peripheral dysostosis", "Acrodysostosis syndrome", "Arkless-Graham syndrome", "Acrodysostosis (disorder)", "Maroteaux-Malamut syndrome", "pug nose-peripheral dysostosis syndrome", "nasal hypoplasia-peripheral dysostosis-mental retardation syndrome", "peripheral dysostosis-nasal hypoplasia-mental retardation syndrome", "Nasal hypoplasia-peripheral dysostosis-mental retardation syndrome", "nasal hypoplasia-peripheral dysostosis-intellectual disability syndrome", "Peripheral dysostosis-nasal hypoplasia-mental retardation (PNM) syndrome", "peripheral dysostosis-nasal hypoplasia-mental retardation (PNM) syndrome", "peripheral dysostosis-nasal hypoplasia-intellectual disability (PNM) syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acrodysostosis", "shortest_name_length": 13}
{"curie": "MONDO:0002840", "names": ["Eosinophilic Gastritis", "Eosinophilic gastritis", "eosinophilic gastritis", "gastritis eosinophilic", "gastritis; eosinophilic", "eosinophilic; gastritis", "Eosinophilic gastritis (disorder)", "eosinophilic gastritis (diagnosis)", "Eosinophilic infiltration in the stomach mucosa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eosinophilic gastritis", "shortest_name_length": 22}
{"curie": "MONDO:0013752", "names": ["HLHS2", "hypoplastic left heart syndrome 2", "HYPOPLASTIC LEFT HEART SYNDROME 2", "hypoplastic left heart syndrome type 2", "NKX2-5 hypoplastic left heart syndrome", "hypoplastic left heart syndrome caused by mutation in NKX2-5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypoplastic left heart syndrome 2", "shortest_name_length": 5}
{"curie": "MONDO:0032892", "names": ["BAIDCS", "structural brain anomalies with impaired intellectual development and craniosynostosis", "STRUCTURAL BRAIN ANOMALIES WITH IMPAIRED INTELLECTUAL DEVELOPMENT AND CRANIOSYNOSTOSIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "structural brain anomalies with impaired intellectual development and craniosynostosis", "shortest_name_length": 6}
{"curie": "MONDO:0020339", "names": ["Complex X-linked HSP", "Complex X-linked SPG", "complicated X-linked HSP", "complicated X-linked SPG", "X-linked complex spastic paraplegia", "X-linked complicated spastic paraplegia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked complex spastic paraplegia", "shortest_name_length": 20}
{"curie": "UMLS:C0854888", "names": ["Relapsed Malignant Peritoneal Mesothelioma", "Recurrent Peritoneal Malignant Mesothelioma", "Peritoneal mesothelioma malignant recurrent", "Malignant Peritoneal Mesothelioma Recurrent", "Relapsed Malignant Mesothelioma of Peritoneum", "Recurrent Malignant Mesothelioma of Peritoneum", "Relapsed Malignant Mesothelioma of the Peritoneum", "Recurrent Malignant Mesothelioma of the Peritoneum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peritoneal mesothelioma malignant recurrent", "shortest_name_length": 42}
{"curie": "UMLS:C4763551", "names": ["Refractory Adenovirus Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Adenovirus Infection", "shortest_name_length": 31}
{"curie": "UMLS:C4727838", "names": ["Advanced Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Melanoma", "shortest_name_length": 17}
{"curie": "UMLS:C5237242", "names": ["BIMT", "BAPoma", "BAP1-Deficient Tumor", "BAP1-Inactivated Melanocytic Tumor", "BAP1-Inactivated Melanocytic Neoplasm", "BAP1-Inactivated Skin Melanocytic Neoplasm", "BAP1-Inactivated Cutaneous Melanocytic Tumor", "BAP1-Inactivated Cutaneous Melanocytic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "BAP1-Inactivated Skin Melanocytic Neoplasm", "shortest_name_length": 4}
{"curie": "UMLS:C1334793", "names": ["Monoblastic Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Monoblastic Sarcoma", "shortest_name_length": 19}
{"curie": "MONDO:0009015", "names": ["CDPD", "CDPD1", "Cdpd1", "HARBOYAN SYNDROME", "Harboyan syndrome", "CORNEAL DYSTROPHY AND PERCEPTIVE DEAFNESS", "Corneal dystrophy and perceptive deafness", "corneal dystrophy and perceptive deafness", "corneal dystrophy with progressive deafness", "Corneal dystrophy with progressive deafness", "CORNEAL DYSTROPHY AND SENSORINEURAL DEAFNESS", "Corneal dystrophy and sensorineural deafness", "corneal dystrophy and sensorineural deafness", "Corneal dystrophy-perceptive deafness syndrome", "corneal dystrophy-perceptive deafness syndrome", "Corneal dystrophy with progressive hearing loss", "Corneal dystrophy and perceptive deafness syndrome", "Corneal dystrophy-perceptive hearing loss syndrome", "corneal endothelial dystrophy and perceptive deafness", "Congenital corneal dystrophy, progressive sensorineural deafness", "congenital corneal dystrophy, progressive sensorineural deafness", "Congenital hereditary endothelial dystrophy and perceptive deafness syndrome", "Congenital hereditary endothelial dystrophy and perceptive deafness syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal dystrophy-perceptive deafness syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C2986536", "names": ["BON", "Bisphosphonate Osteonecrosis", "Bisphosphonate Osteonecroses", "Osteonecroses, Bisphosphonate", "Osteonecrosis, Bisphosphonate", "Bisphosphonate-Associated Osteonecroses", "Bisphosphonate-Associated Osteonecrosis", "bisphosphonate-associated osteonecrosis", "Bisphosphonate-associated osteonecrosis", "Bisphosphonate Associated Osteonecrosis", "Osteonecrosis, Bisphosphonate-Associated", "Osteonecroses, Bisphosphonate-Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bisphosphonate-associated osteonecrosis", "shortest_name_length": 3}
{"curie": "MONDO:0012471", "names": ["AGS3", "Aicardi-Goutieres syndrome 3", "AICARDI-GOUTIERES SYNDROME 3", "Aicardi-Goutieres Syndrome 3", "Aicardi-Goutieres syndrome type 3", "RNASEH2C Aicardi-Goutieres syndrome", "RNASEH2C -related Aicardi-Goutieres syndrome", "Aicardi-Goutieres syndrome caused by mutation in RNASEH2C"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aicardi-Goutieres syndrome 3", "shortest_name_length": 4}
{"curie": "UMLS:C2827468", "names": ["Congenital Artery Disease", "Congenital Coronary Artery Abnormality"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Coronary Artery Abnormality", "shortest_name_length": 25}
{"curie": "MONDO:0016460", "names": ["PHD syndrome", "polyvalvular heart disease syndrome", "Polyvalvular heart disease syndrome", "Polyvalvular heart disease syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyvalvular heart disease syndrome", "shortest_name_length": 12}
{"curie": "UMLS:C1513483", "names": ["Monosomy 7", "Chromosome 7, monosomy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chromosome 7, monosomy", "shortest_name_length": 10}
{"curie": "MONDO:0023101", "names": ["facio digito genital syndrome recessive form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "facio digito genital syndrome recessive form", "shortest_name_length": 44}
{"curie": "MONDO:0015206", "names": ["Rommen Mueller Sybert syndrome", "Rommen-Mueller-Sybert syndrome", "short stature heart defect and craniofacial anomalies", "Short stature, heart defect and craniofacial anomalies", "short stature-heart defect-craniofacial anomalies syndrome", "Developmental delay, growth deficiency, congenital heart defect, and multiple craniofacial anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short stature-heart defect-craniofacial anomalies syndrome", "shortest_name_length": 30}
{"curie": "UMLS:C4744709", "names": ["Parotid Gland Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parotid Gland Liposarcoma", "shortest_name_length": 25}
{"curie": "MONDO:0016298", "names": ["Isolated postlingual genetic deafness", "isolated postlingual genetic deafness", "postlingual non-syndromic genetic deafness", "Postlingual non-syndromic genetic deafness", "postlingual non-syndromic genetic hearing loss", "Postlingual non-syndromic genetic deafness (disorder)", "Postlingual non-syndromic genetic deafness (diagnosis)", "sensorineural hearing loss postlingual non-syndromic genetic deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postlingual non-syndromic genetic hearing loss", "shortest_name_length": 37}
{"curie": "MONDO:0020643", "names": ["AUTS1", "autism susceptibility 1", "autism susceptibility 1, isolated cases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autism susceptibility 1", "shortest_name_length": 5}
{"curie": "MONDO:0012742", "names": ["BRGDA3", "Brugada syndrome 3", "Brugada Syndrome 3", "BRUGADA SYNDROME 3", "Brugada syndrome type 3", "CACNA1C Brugada syndrome", "Brugada syndrome 3 (diagnosis)", "Brugada syndrome caused by mutation in CACNA1C"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brugada syndrome 3", "shortest_name_length": 6}
{"curie": "MONDO:0006888", "names": ["Carcinomatous neuropathy", "Paraneoplastic Neuropathy", "paraneoplastic neuropathy", "Paraneoplastic neuropathy", "neuropathy paraneoplastic", "Neuropathy, Paraneoplastic", "Paraneoplastic Neuropathies", "Polyneuropathy in malignancy", "Neuropathies, Paraneoplastic", "Paraneoplastic Polyneuropathy", "paraneoplastic polyneuropathy", "Paraneoplastic polyneuropathy", "Polyneuropathy, Paraneoplastic", "Paraneoplastic Polyneuropathies", "Polyneuropathies, Paraneoplastic", "Polyneuropathy in malignant disease", "Carcinomatous peripheral neuropathy", "Paraneoplastic neuropathy (disorder)", "paraneoplastic neuropathy peripheral", "Peripheral neuropathy, carcinomatous", "Paraneoplastic peripheral neuropathy", "Paraneoplastic Peripheral Neuropathy", "paraneoplastic neuropathy (diagnosis)", "Neuropathy, Paraneoplastic Peripheral", "Peripheral Neuropathy, Paraneoplastic", "Paraneoplastic Peripheral Neuropathies", "Neuropathies, Paraneoplastic Peripheral", "polyneuropathy due to malignant disease", "Peripheral Neuropathies, Paraneoplastic", "Paraneoplastic peripheral neuropathy (disorder)", "Paraneoplastic peripheral neuropathy (diagnosis)", "polyneuropathy due to malignant disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paraneoplastic polyneuropathy", "shortest_name_length": 24}
{"curie": "MONDO:0012241", "names": ["PEOA3", "autosomal dominant progressive external ophthalmoplegia 3", "PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL DOMINANT 3", "progressive external ophthalmoplegia, autosomal dominant 3", "Progressive External Ophthalmoplegia, Autosomal Dominant, 3", "TWNK progressive external ophthalmoplegia with mitochondrial DNA deletions", "autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3", "PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3", "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3", "Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3", "progressive external ophthalmoplegia with mitochondrial DNA deletions caused by mutation in TWNK", "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3", "shortest_name_length": 5}
{"curie": "MONDO:0007984", "names": ["MDMHB", "metaphyseal dysplasia maxillary hypoplasia brachydactyly", "metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome", "metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly", "METAPHYSEAL DYSPLASIA WITH MAXILLARY HYPOPLASIA WITH OR WITHOUT BRACHYDACTYLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0855012", "names": ["Chondrosarcoma metastatic", "Metastatic Chondrosarcoma", "Chondrosarcoma, Metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chondrosarcoma metastatic", "shortest_name_length": 25}
{"curie": "UMLS:C5555060", "names": ["BCOR ITD Sarcoma", "BCOR-ITD Sarcoma", "Sarcoma with BCOR Internal Tandem Duplication", "Round Cell Sarcoma with BCOR Internal Tandem Duplication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "BCOR ITD Sarcoma", "shortest_name_length": 16}
{"curie": "MONDO:0012570", "names": ["PXE-like syndrome", "pseudoxanthoma elasticum-like syndrome", "Pseudoxanthoma elasticum-like syndrome", "PXE (pseudoxanthoma elasticum) like syndrome", "PXE-like disorder with multiple coagulation Factor deficiency", "PXE-LIKE DISORDER WITH MULTIPLE COAGULATION FACTOR DEFICIENCY", "PXE-Like Disorder with Multiple Coagulation Factor Deficiency", "Body skin hyperlaxity due to vitamin K dependent coagulation factor deficiency", "body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency", "Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency", "PSEUDOXANTHOMA ELASTICUM-LIKE DISORDER WITH MULTIPLE COAGULATION FACTOR DEFICIENCY", "Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency", "pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency", "Body skin hyperlaxity due to vitamin K dependent coagulation factor deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency", "shortest_name_length": 17}
{"curie": "MONDO:0011753", "names": ["EIG2", "idiopathic generalized epilepsy 2", "EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 2", "epilepsy, idiopathic generalized, susceptibility to, 2", "EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, LOCUS ON CHROMOSOME 14", "epilepsy, idiopathic generalized, susceptibility to, locus on chromosome 14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, idiopathic generalized, susceptibility to, 2", "shortest_name_length": 4}
{"curie": "UMLS:C2204527", "names": ["Floor of Mouth BSCC", "Floor of Mouth Basaloid Squamous Cell Carcinoma", "basaloid squamous cell carcinoma of floor of mouth", "basaloid squamous cell carcinoma of floor of mouth (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "basaloid squamous cell carcinoma of floor of mouth", "shortest_name_length": 19}
{"curie": "MONDO:0019191", "names": ["Mikulicz", "Mikulicz disease", "Mikulicz Disease", "Mikulicz' disease", "mikulicz syndrome", "Mikuliczs Disease", "MIKULICZ SYNDROME", "Mikulicz syndrome", "Mikulicz' Disease", "Mikulicz's Disease", "mikulicz's disease", "Mikulicz's disease", "mikulicz's syndrome", "Mikulicz's syndrome", "Mikulicz's Syndrome", "Mikulicz disease (former)", "Mikulicz syndrome (former)", "Mikulicz's disease (former)", "Mikulicz disease (diagnosis)", "Mikulicz's disease (disorder)", "Chronic dacryoadenitis and sialadenitis", "chronic dacryoadenitis and sialadenitis", "IgG4-related dacryoadenitis and sialadenitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IgG4-related dacryoadenitis and sialadenitis", "shortest_name_length": 8}
{"curie": "MONDO:0032737", "names": ["SPG80", "hereditary spastic paraplegia 80", "spastic paraplegia 80 autosomal dominant", "SPASTIC PARAPLEGIA 80, AUTOSOMAL DOMINANT", "spastic paraplegia 80, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic paraplegia 80, autosomal dominant", "shortest_name_length": 5}
{"curie": "UMLS:C4687446", "names": ["Refractory Glioblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Glioblastoma", "shortest_name_length": 23}
{"curie": "UMLS:C0861212", "names": ["Recurrent Centroblastic Lymphoma", "Centroblastic lymphoma recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Centroblastic lymphoma recurrent", "shortest_name_length": 32}
{"curie": "UMLS:C5205693", "names": ["CAMSG", "Cribriform Adenocarcinoma of Minor Salivary Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cribriform Adenocarcinoma of Minor Salivary Gland", "shortest_name_length": 5}
{"curie": "UMLS:C1332289", "names": ["Anaplastic Renal Wilms Tumor", "Anaplastic Renal Wilms' Tumor", "Anaplastic Kidney Wilms Tumor", "Anaplastic Renal Wilm's Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anaplastic Kidney Wilms Tumor", "shortest_name_length": 28}
{"curie": "UMLS:C0160427", "names": ["injury of kidney with open wound into cavity", "Injury to Kidney with Open Wound into Cavity", "Injury to kidney with open wound into cavity", "Unspecified injury to kidney with open wound into cavity", "injury of kidney with open wound into cavity (diagnosis)", "Injury to kidney with open wound into cavity, unspecified injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury to kidney with open wound into cavity", "shortest_name_length": 44}
{"curie": "MONDO:0014329", "names": ["ATRST2", "atrial standstill 2", "ATRIAL STANDSTILL 2", "NPPA atrial standstill", "atrial standstill type 2", "atrial dilation and standstill", "ATRIAL DILATION AND STANDSTILL", "atrial standstill caused by mutation in NPPA", "cardiomyopathy, atrial dilated, with atrial standstill", "CARDIOMYOPATHY, ATRIAL DILATED, WITH ATRIAL STANDSTILL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial standstill 2", "shortest_name_length": 6}
{"curie": "MONDO:0003562", "names": ["rete testis tumor", "Rete Testis Neoplasm", "tumor of rete testis", "rete testis neoplasm", "neoplasm of rete testis", "rete testis neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rete testis neoplasm", "shortest_name_length": 17}
{"curie": "UMLS:C0751010", "names": ["Cerebral Infarction, Left Hemisphere", "Left Hemisphere, Cerebral Infarction", "Cerebral, Left Hemisphere, Infarction", "Infarction, Cerebral, Left Hemisphere", "Left Hemisphere, Infarction, Cerebral", "Infarction, Left Hemisphere, Cerebral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebral Infarction, Left Hemisphere", "shortest_name_length": 36}
{"curie": "UMLS:C0684517", "names": ["Benign Skull Neoplasm", "benign neoplasm of skull", "Benign neoplasm of bone of skull", "benign neoplasm of skull (diagnosis)", "Benign neoplasm of bone of skull, NOS", "Benign neoplasm of bone of skull (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign neoplasm of bone of skull", "shortest_name_length": 21}
{"curie": "MONDO:0010696", "names": ["omphalocele, X-linked", "OMPHALOCELE, X-LINKED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "omphalocele, X-linked", "shortest_name_length": 21}
{"curie": "MONDO:0030849", "names": ["IDDSAPN", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY AND AXONAL PERIPHERAL NEUROPATHY", "intellectual developmental disorder with speech delay and axonal peripheral neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder with speech delay and axonal peripheral neuropathy", "shortest_name_length": 7}
{"curie": "UMLS:C1322018", "names": ["fallopian tube cancer stage IV", "Fallopian Tube Cancer Stage IV", "Stage IV Fallopian Tube Cancer", "stage IV fallopian tube cancer", "metastatic fallopian tube cancer", "AJCC stage IV fallopian tube cancer", "AJCC Stage IV Fallopian Tube Cancer", "metastatic fallopian tube carcinoma", "FIGO Stage IV Fallopian Tube Carcinoma", "Stage IV Fallopian Tube Cancer AJCC v6", "stage IV fallopian tube cancer AJCC v7", "stage IV fallopian tube cancer AJCC v6", "FIGO stage IV fallopian tube carcinoma", "Stage IV Fallopian Tube Cancer AJCC v7", "FIGO stage IV carcinoma of fallopian tube", "FIGO Stage IV Carcinoma of Fallopian Tube", "FIGO stage IV carcinoma of the fallopian tube", "FIGO Stage IV Carcinoma of the Fallopian Tube", "Stage IV Fallopian Tube Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Fallopian Tube Cancer AJCC v6 and v7", "shortest_name_length": 30}
{"curie": "MONDO:0008931", "names": ["CLSS", "Cenani syndactyly", "syndactyly type 7", "Syndactyly type 7", "syndactyly, type 7", "Cenani syndactylism", "CENANI SYNDACTYLISM", "SYNDACTYLY, TYPE VII", "Cenani Lenz syndrome", "Syndactyly, Type VII", "Cenani-Lenz syndrome", "CENANI-LENZ SYNDACTYLY", "Cenani-Lenz Syndactyly", "Cenani-Lenz syndactyly", "Cenani Lenz syndactyly", "Syndactyly Cenani Lenz type", "syndactyly Cenani Lenz type", "Cenani-Lenz type syndactyly", "Syndactyly type 7 (disorder)", "syndactyly type 7 (diagnosis)", "CENANI-LENZ SYNDACTYLY SYNDROME", "Cenani-Lenz syndactyly syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cenani-Lenz syndactyly syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0006065", "names": ["LACTASE PERSISTENCE", "Primary hypolactasia", "Hypolactasia, Adult Type", "adult lactase deficiency", "HYPOLACTASIA, ADULT TYPE", "ADULT LACTASE DEFICIENCY", "Adult lactase deficiency", "Adult Lactase Deficiency", "hypolactasia, adult type", "disaccharide intolerance 3", "DISACCHARIDE INTOLERANCE III", "Disaccharide intolerance III", "Disaccharide Intolerance III", "Late onset lactase deficiency", "lactose intolerance adult type", "Late-onset lactose intolerance", "Lactose Intolerance, Adult Type", "lactose intolerance, ADULT type", "LACTOSE INTOLERANCE, ADULT TYPE", "lactase persistence/nonpersistence", "Nonpersistence of intestinal lactase", "Non-persistence of intestinal lactase", "Ontogenic late onset lactase deficiency", "Delayed-onset isolated lactase deficiency", "Disaccharide intolerance syndrome, type III", "Nonpersistence of intestinal lactase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lactose intolerance adult type", "shortest_name_length": 19}
{"curie": "UMLS:C5239112", "names": ["Recurrent Nodal Peripheral T-Cell Lymphoma with TFH Phenotype"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Nodal Peripheral T-Cell Lymphoma with TFH Phenotype", "shortest_name_length": 61}
{"curie": "MONDO:0021164", "names": ["POSTHITIS", "Posthitis", "posthitis", "Posthitis NOS", "Posthitis, NOS", "Prepuce inflamed", "Posthitis (disorder)", "Inflammation of prepuce", "prepuce of penis inflammation", "inflammation of prepuce of penis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "posthitis", "shortest_name_length": 9}
{"curie": "MONDO:0011562", "names": ["PARK4", "Park4", "Parkinson's disease 4", "autosomal dominant Parkinson disease 4", "Parkinson disease 4, autosomal dominant", "PARKINSON DISEASE 4, AUTOSOMAL DOMINANT", "autosomal dominant Parkinson's disease 4", "autosomal dominant Parkinson disease type 4", "autosomal dominant Lewy body Parkinson disease 4", "PARKINSON DISEASE 4, AUTOSOMAL DOMINANT LEWY BODY", "Parkinson disease 4, autosomal dominant Lewy body", "Parkinson Disease 4, Autosomal Dominant Lewy Body"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant Parkinson disease 4", "shortest_name_length": 5}
{"curie": "UMLS:C5419605", "names": ["Locally Advanced Esophageal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Esophageal Squamous Cell Carcinoma", "shortest_name_length": 51}
{"curie": "MONDO:0017223", "names": ["transitional PMD", "Pelizaeus-Merzbacher disease, transitional form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pelizaeus-Merzbacher disease, transitional form", "shortest_name_length": 16}
{"curie": "UMLS:C0267387", "names": ["Fulminant ulcerative colitis", "Severe chronic ulcerative colitis", "ulcerative colitis chronic severe", "Severe chronic ulcerative colitis (disorder)", "Severe chronic ulcerative colitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Severe chronic ulcerative colitis", "shortest_name_length": 28}
{"curie": "MONDO:0044336", "names": ["colorectal signet Ring cell carcinoma", "colorectal signet ring cell carcinoma", "Colorectal Signet-Ring Cell Carcinoma", "Colorectal Signet Ring Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorectal signet ring cell carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0007755", "names": ["hyperimmunoglobulin G1 syndrome", "HYPERIMMUNOGLOBULIN G1(A1) SYNDROME", "Hyperimmunoglobulin G1(A1) Syndrome", "hyperimmunoglobulin G1(A1) syndrome", "Immunoglobulin heavy chain regulator"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperimmunoglobulin G1(A1) syndrome", "shortest_name_length": 31}
{"curie": "MONDO:0005172", "names": ["osteoarthropathy", "Osteoarthropathy", "skeletal disorder", "disorders skeletal", "Osteoarthropathies", "bone joint disease", "bone diseases joint", "BONE/JOINT DISORDERS", "bone joint disorders", "bones joints diseases", "Osteoarthropathy, NOS", "bones diseases joints", "Skeletal system disease", "skeletal system disease", "disease skeletal system", "diseases skeletal system", "skeletal system disorder", "disorders skeletal system", "Disease of bone and joint", "disease of skeletal system", "Disorder of skeletal system", "disorder of skeletal system", "disease of bone and/or joint", "Diseases of Bones and Joints", "Disease of bone AND/OR joint", "Disease of bone and joint, NOS", "Disease of skeletal system, NOS", "Disorder of skeletal system, NOS", "skeletal system disease or disorder", "Disease or syndrome of skeletal system", "disease or disorder of skeletal system", "Disorder of skeletal system (disorder)", "disorder of skeletal system (diagnosis)", "Diseases and Syndromes of Skeletal System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skeletal system disorder", "shortest_name_length": 16}
{"curie": "MONDO:0011275", "names": ["AMDM", "AMD1", "ST. HELENA DYSPLASIA", "St. Helena dysplasia", "ACROMESOMELIC DYSPLASIA 1", "acromesomelic dysplasia-1", "Acromesomelic dwarfism Maroteux type", "acromesomelic dwarfism Maroteux type", "acromesomelic dysplasia Maroteaux type", "Acromesomelic dysplasia Maroteaux type", "acromesomelic dysplasia, Maroteaux type", "Acromesomelic dysplasia, Maroteaux type", "ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE", "acromesomelic dysplasia 1, Maroteaux type", "Acromesomelic dysplasia Maroteaux type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acromesomelic dysplasia 1, Maroteaux type", "shortest_name_length": 4}
{"curie": "MONDO:0010365", "names": ["CFTDX", "X-linked congenital myopathy with fiber-type disproportion", "MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION, X-LINKED", "myopathy, congenital, with fiber-type disproportion, X-linked", "Myopathy, Congenital, With Fiber-Type Disproportion, X-Linked", "myopathy, congenital, with fiber-type disproportion, X-linked, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy, congenital, with fiber-type disproportion, X-linked", "shortest_name_length": 5}
{"curie": "UMLS:C3203733", "names": ["Texidor Twinge", "Texidor's twinge", "Texidor's Twinge", "Precordial Catch", "Precordial catch syndrome", "precordial catch syndrome", "Precordial Catch Syndrome", "Syndrome, Precordial Catch", "precordial catch syndrome (diagnosis)", "Musculoskeletal chest pain: idiopathic/precordial catch syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Precordial Catch Syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C3897538", "names": ["Stage II Oropharyngeal Lymphoepithelioma", "Stage II Oropharyngeal Lymphoepithelioma AJCC v7", "Stage II Oropharyngeal Lymphoepithelioma AJCC v6", "Stage II Oropharyngeal Undifferentiated Carcinoma", "Stage II Undifferentiated Oropharyngeal Throat Cancer", "Stage II Oropharyngeal Undifferentiated Carcinoma AJCC v6", "Stage II Oropharyngeal Undifferentiated Carcinoma AJCC v7", "Stage II Oropharyngeal Undifferentiated Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Oropharyngeal Undifferentiated Carcinoma AJCC v6 and v7", "shortest_name_length": 40}
{"curie": "MONDO:0007268", "names": ["CMH4", "hypertrophic cardiomyopathy 4", "cardiomyopathy, hypertrophic, 4", "hypertrophic cardiomyopathy type 4", "MYBPC3 hypertrophic cardiomyopathy", "cardiomyopathy, familial hypertrophic, 4", "Cardiomyopathy, Familial Hypertrophic, 4", "CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4", "Familial Hypertrophic Cardiomyopathy Type 4", "familial hypertrophic cardiomyopathy type 4", "cardiomyopathy, familial hypertrophic, type 4", "hypertrophic cardiomyopathy caused by mutation in MYBPC3", "CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4, SUSCEPTIBILITY TO", "cardiomyopathy, familial hypertrophic, 4, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophic cardiomyopathy 4", "shortest_name_length": 4}
{"curie": "MONDO:0002989", "names": ["Xanthofibroma", "fibroxanthoma", "FIBROXANTHOMA", "Fibroxanthoma", "xanthofibroma", "Fibroxanthoma, NOS", "fibrous histiocytoma", "Fibrous Histiocytoma", "Fibrous histiocytoma", "FIBROUS HISTIOCYTOMA", "fibrous histiocytomas", "Fibrous Histiocytomas", "Histiocytoma, Fibrous", "Histiocytomas, Fibrous", "Fibrous histiocytoma NOS", "Fibrous histiocytoma, NOS", "Benign fibrous histiocytoma", "Benign Fibrous Histiocytoma", "benign fibrous histiocytoma", "Histiocytoma, Benign Fibrous", "Fibrous Histiocytoma, Benign", "Benign Fibrous Histiocytomas", "Histiocytomas, Benign Fibrous", "Fibrous Histiocytomas, Benign", "HISTIOCYTOMA, FIBROUS, BENIGN", "histiocytoma, fibrous, benign", "fibroxanthoma NOS (morphologic abnormality)", "fibrous histiocytoma NOS (morphologic abnormality)", "Benign fibrous histiocytoma (morphologic abnormality)", "benign fibrous histiocytoma (morphologic abnormality)", "Fibrous histiocytoma, no ICD subtype (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign fibrous histiocytoma", "shortest_name_length": 13}
{"curie": "MONDO:0019475", "names": ["SPTCL", "subcutaneous panniculitic T-cell lymphoma", "Subcutaneous panniculitic T-cell lymphoma", "subcutaneous panniculitis-like T-cell lymphoma", "Subcutaneous Panniculitis-Like T-Cell Lymphoma", "Subcutaneous panniculitis-like T-cell lymphoma", "T-CELL LYMPHOMA, SUBCUTANEOUS PANNICULITIS-LIKE", "Subcutaneous panniculitic cutaneous T-cell lymphoma", "subcutaneous panniculitis-like T-cell lymphoma (diagnosis)", "Subcutaneous panniculitic cutaneous T-cell lymphoma (disorder)", "Subcutaneous Panniculitis-Like T-Cell Lymphoma, Alpha/Beta Type", "subcutaneous panniculitis-like T-cell lymphoma, Alpha/Beta type", "subcutaneous panniculitis-like T-cell lymphoma (Alpha/Beta type)", "Subcutaneous Panniculitis-Like T-Cell Lymphoma (Alpha/Beta Type)", "Subcutaneous panniculitic T-cell lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subcutaneous panniculitis-like T-cell lymphoma", "shortest_name_length": 5}
{"curie": "UMLS:C1336395", "names": ["Stage IVC Larynx Epidermoid Carcinoma", "Stage IVC Epidermoid Carcinoma of Larynx", "Stage IVC Laryngeal Epidermoid Carcinoma", "Stage IVC Larynx Squamous Cell Carcinoma", "Stage IVC Squamous Cell Carcinoma of Larynx", "Stage IVC Laryngeal Squamous Cell Carcinoma", "Stage IVC Epidermoid Carcinoma of the Larynx", "Stage IVC Squamous Cell Carcinoma of the Larynx", "Stage IVC Laryngeal Throat Squamous Cell Cancer", "Stage IVC Laryngeal Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Laryngeal Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 37}
{"curie": "MONDO:0013868", "names": ["POROK7", "POROKERATOSIS 7, MULTIPLE TYPES", "porokeratosis 7, multiple types", "porokeratosis 7, disseminated superficial actinic type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "porokeratosis 7, multiple types", "shortest_name_length": 6}
{"curie": "UMLS:C3273035", "names": ["Poorly Differentiated Hepatocellular Cancer", "Poorly Differentiated Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Poorly Differentiated Hepatocellular Carcinoma", "shortest_name_length": 43}
{"curie": "UMLS:C2363775", "names": ["Rabbit syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rabbit syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0014562", "names": ["COQ10D7", "primary coenzyme Q10 deficiency 7", "coenzyme Q10 deficiency, primary, 7", "COENZYME Q10 DEFICIENCY, PRIMARY, 7", "COQ4-related neonatal encephalomyopathy", "coenzyme Q10 deficiency, primary, type 7", "Coenzyme Q4-related neonatal encephalomyopathy", "neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome", "Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome", "Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome", "Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome", "shortest_name_length": 7}
{"curie": "MONDO:0004459", "names": ["bladder hepatoid adenocarcinoma", "Bladder Hepatoid Adenocarcinoma", "hepatoid adenocarcinoma of bladder", "hepatoid adenocarcinoma of bladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder hepatoid adenocarcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0019722", "names": ["GLOMERULAR", "glomerulopathy", "Glomerulopathy", "GLOMERULOPATHY", "glomerulopathies", "glomerular disease", "Diseased glomeruli", "Glomerular disease", "GLOMERULAR DISEASE", "glomerular disorder", "glomerular; disease", "Glomerular diseases", "glomerular diseases", "Glomerulonephropathy", "glomerulonephropathy", "GLOMERULONEPHROPATHY", "glomerular disease NOS", "renal glomerular disease", "renal glomerulus disease", "Renal glomerular disease", "RENAL GLOMERULAR DISEASES", "glomerulopathy (diagnosis)", "disease of renal glomerulus", "disorder of renal glomerulus", "Glomerular disease (disorder)", "Renal glomerular disease, NOS", "Glomerular diseases (N00-N08)", "Renal glomerular syndrome, NOS", "glomerular disease (diagnosis)", "Renal glomerular disorder, NOS", "Renal glomerular disease or syndrome", "renal glomerulus disease or disorder", "disease or disorder of renal glomerulus", "Renal Glomerular Diseases and Syndromes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glomerular disorder", "shortest_name_length": 10}
{"curie": "EFO:1001513", "names": ["liver neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "liver neoplasm", "shortest_name_length": 14}
{"curie": "MONDO:0021096", "names": ["papillary epithelial neoplasm", "Papillary Epithelial Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papillary epithelial neoplasm", "shortest_name_length": 29}
{"curie": "MONDO:0024334", "names": ["peripheral nerve lesion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peripheral nerve lesion", "shortest_name_length": 23}
{"curie": "UMLS:C2828016", "names": ["Stage IIIA Merkel Cell Carcinoma", "Stage IIIA Merkel Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Merkel Cell Carcinoma AJCC v7", "shortest_name_length": 32}
{"curie": "MONDO:0006781", "names": ["Helicobacter infection", "helicobacter infection", "Helicobacter Infection", "Helicobacter Infections", "Infection, Helicobacter", "helicobacter infections", "infection, Helicobacter", "Helicobacter infections", "infections, Helicobacter", "Infections, Helicobacter", "Helicobacter pylori infectious disease", "Helicobacter pylori disease or disorder", "Helicobacter pylori caused disease or disorder", "Helicobacter pylori infection, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Helicobacter pylori infectious disease", "shortest_name_length": 22}
{"curie": "UMLS:C1335014", "names": ["Non-Neoplastic Head and Neck Disease", "Non-Neoplastic Head and Neck Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Head and Neck Disorder", "shortest_name_length": 36}
{"curie": "UMLS:C0854762", "names": ["Relapsed Esophagus Adenocarcinoma", "Relapsed Esophageal Adenocarcinoma", "Recurrent Esophagus Adenocarcinoma", "Esophageal adenocarcinoma recurrent", "Recurrent Esophageal Adenocarcinoma", "Relapsed Adenocarcinoma of Esophagus", "Oesophageal adenocarcinoma recurrent", "Esophageal Adenocarcinoma, Recurrent", "Oesophageal Adenocarcinoma Recurrent", "Recurrent Adenocarcinoma of Esophagus", "Relapsed Adenocarcinoma of the Esophagus", "Recurrent Adenocarcinoma of the Esophagus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal adenocarcinoma recurrent", "shortest_name_length": 33}
{"curie": "UMLS:C0206142", "names": ["eosinophil leukemia", "Eosinophil leukemia", "eosinophils leukemia", "Eosinophil leukaemia", "leukemia eosinophilic", "Leukemia eosinophilic", "EOSINOPHILIC LEUKEMIA", "eosinophilic leukemia", "Eosinophilic leukemia", "LEUKEMIA EOSINOPHILIC", "Eosinophilic Leukemia", "Leukaemia eosinophilic", "Eosinophilic leukaemia", "eosinophilic leukaemia", "LEUKEMIA, EOSINOPHILIC", "Eosinophilic Leukemias", "eosinophilic; leukemia", "leukemia; eosinophilic", "Leukemia, Eosinophilic", "Leukemias, Eosinophilic", "eosinophilic leukemia (diagnosis)", "Eosinophilic leukemia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eosinophilic leukemia", "shortest_name_length": 19}
{"curie": "MONDO:0043452", "names": ["tri8", "8 trisomy", "trisomy 8", "Trisomy 8", "Warkany syndrome 2", "Trisomy C syndrome", "TRISOMY 8 SYNDROME", "trisomy 8 syndrome", "Trisomy 8 syndrome", "Trisomy 8 (disorder)", "Chromosome 8 trisomy", "trisomy 8 (diagnosis)", "chromosome 8, trisomy", "Chromosome 8, trisomy", "chromosome 8 duplication", "Chromosome 8 duplication", "chromosome 8 trisomy syndrome", "Chromosomal imbalance syndrome, pair 8, trisomy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 8, trisomy", "shortest_name_length": 4}
{"curie": "UMLS:C5237386", "names": ["AVL", "Atypical Vascular Lesion", "Benign Lymphangiomatous Papule", "Atypical Vascular Proliferation", "Post-Radiation Therapy Lymphangioma", "Post-Radiation Therapy Lymphangiectasia", "Benign Vascular Lesion in Previously Irradiated Skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypical Vascular Proliferation", "shortest_name_length": 3}
{"curie": "UMLS:C1882107", "names": ["Non-Neoplastic Intestinal Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Intestinal Disorder", "shortest_name_length": 34}
{"curie": "UMLS:C0027055", "names": ["Myocardial reperfusion injury", "Myocardial Reperfusion Injury", "Injury, Myocardial Reperfusion", "Reperfusion Injury, Myocardial", "Myocardial Reperfusion Injuries", "Reperfusion Injuries, Myocardial", "Injuries, Myocardial Reperfusion", "Myocardial Ischemic Reperfusion Injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myocardial Reperfusion Injury", "shortest_name_length": 29}
{"curie": "MONDO:0015688", "names": ["Myeloid/Lymphoid Neoplasms with Eosinophilia and Gene Rearrangement", "myeloid/lymphoid neoplasms with eosinophilia and gene rearrangement", "myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, or FGFR1", "Myeloid and Lymphoid Neoplasms with Eosinophilia and Abnormalities of PDGFRA, PDGFRB, or FGFR1", "myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1", "myeloid/lymphoid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB, FGFR1 or JAK2", "Myeloid/Lymphoid Neoplasms with Eosinophilia and Rearrangement of PDGFRA, PDGFRB, or FGFR1, or with PCM1-JAK2", "myeloid/lymphoid neoplasms with eosinophilia and rearrangement of PDGFRA, PDGFRB, or FGFR1, or with PCM1-JAK2", "Myeloid and Lymphoid Neoplasms with Eosinophilia and Rearrangement of PDGFRA, PDGFRB, or FGFR1, or with PCM1-JAK2", "myeloid and lymphoid neoplasms with eosinophilia and rearrangement of PDGFRA, PDGFRB, or FGFR1, or with PCM1-JAK2", "Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of platelet-derived growth factor receptor alpha (PDGFRA), platelet-derived growth factor receptor beta (PDGFRB), and fibroblast growth factor receptor-1 (FGFR1) are a group of hematologic neoplasms", "myeloid and lymphoid neoplasms with eosinophilia and abnormalities of platelet-derived growth factor receptor alpha (PDGFRA), platelet-derived growth factor receptor beta (PDGFRB), and fibroblast growth factor receptor-1 (FGFR1) are a group of hematologic neoplasms"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myeloid/lymphoid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB, FGFR1 or JAK2", "shortest_name_length": 67}
{"curie": "UMLS:C0274859", "names": ["Inorganic Mercury Poisoning", "Inorganic mercury poisoning", "Poisoning, Inorganic Mercury", "Mercury Poisoning, Inorganic", "Inorganic mercury poisoning (disorder)", "Inorganic mercury compound causing toxic effect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Inorganic Mercury Poisoning", "shortest_name_length": 27}
{"curie": "MONDO:0012848", "names": ["MKS6", "Meckel syndrome 6", "Meckel syndrome type 6", "CC2D2A Meckel syndrome", "Meckel Syndrome, Type 6", "MECKEL SYNDROME, TYPE 6", "Meckel syndrome, type 6", "Meckel-Gruber syndrome, type 6", "MECKEL SYNDROME, TYPE 6 (disorder)", "Meckel syndrome type 6 (diagnosis)", "Meckel syndrome caused by mutation in CC2D2A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meckel syndrome, type 6", "shortest_name_length": 4}
{"curie": "UMLS:C4054544", "names": ["Mesangiocapillary Glomerulonephritis Type 3", "Membranoproliferative Glomerulonephritis Type 3 (AQ)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Membranoproliferative Glomerulonephritis Type 3 (AQ)", "shortest_name_length": 43}
{"curie": "MONDO:0002843", "names": ["fungal gastritis", "Gastritis fungal", "Fungal gastritis", "Fungal Gastritis", "Gastritis fungal NOS", "Fungi gastritis (disease)", "Gastritis caused by fungus", "Fungi caused gastritis (disease)", "Gastritis caused by fungus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fungal gastritis", "shortest_name_length": 16}
{"curie": "MONDO:0012043", "names": ["RBCD", "CDB1", "CDRB", "Reis-Bucklers dystrophy", "Reis Bucklers dystrophy", "corneal dystrophy geographic", "CDB type I corneal dystrophy", "Geographic corneal dystrophy", "geographic corneal dystrophy", "CORNEAL DYSTROPHY, GEOGRAPHIC", "corneal dystrophy, geographic", "Corneal dystrophy, geographic", "Reis-Buckler corneal dystrophy", "Reis Bucklers corneal dystrophy", "Reis-Bucklers corneal dystrophy", "Reis-Bücklers corneal dystrophy", "REIS-BUCKLERS CORNEAL DYSTROPHY", "corneal dystrophy Reis-Bucklers'", "Reis-Bucklers' corneal dystrophy", "granular corneal dystrophy type 3", "Granular corneal dystrophy type 3", "granular corneal dystrophy, type 3", "atypical granular corneal dystrophy", "granular corneal dystrophy type III", "Granular corneal dystrophy type III", "Atypical granular corneal dystrophy", "Granular Corneal Dystrophy, Type III", "corneal dystrophy Reis Bucklers type", "GRANULAR CORNEAL DYSTROPHY, TYPE III", "Corneal dystrophy, Reis-Bucklers type", "CORNEAL DYSTROPHY, REIS-BUCKLERS TYPE", "corneal dystrophy, REIS-Bucklers type", "Superficial granular corneal dystrophy", "superficial granular corneal dystrophy", "corneal dystrophy of Bowman layer type I", "Corneal dystrophy of Bowman layer type 1", "corneal dystrophy of Bowman layer type 1", "Corneal dystrophy of Bowman layer type I", "corneal dystrophy of Bowman Layer, type 1", "Corneal dystrophy of Bowman layer, type 1", "Corneal Dystrophy Of Bowman Layer, Type I", "CORNEAL DYSTROPHY OF BOWMAN LAYER, TYPE I", "corneal dystrophy epithelial Reis-Buckler", "Reis-Bucklers' corneal dystrophy (disorder)", "anterior limiting membrane dystrophy type I", "anterior limiting membrane dystrophy type 1", "Anterior limiting membrane dystrophy type 1", "Anterior limiting membrane dystrophy type I", "Reis-Bucklers' corneal dystrophy (diagnosis)", "Reis-Buckler corneal dystrophy (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reis-Bucklers corneal dystrophy", "shortest_name_length": 4}
{"curie": "MONDO:0024455", "names": ["DRS1", "Robinow dwarfism", "fetal face syndrome", "autosomal dominant Robinow syndrome 1", "ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1", "Robinow syndrome, autosomal dominant 1", "WNT5A autosomal dominant Robinow syndrome", "acral dysostosis with Facial and genital abnormalities", "dysostosis acral with facial and genital abnormalities", "autosomal dominant Robinow syndrome caused by mutation in WNT5A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant Robinow syndrome 1", "shortest_name_length": 4}
{"curie": "MONDO:0020679", "names": ["Conduction deafness", "Conductive Deafness", "conductive deafness", "Deafness;conductive", "Conductive deafness", "deafness; conduction", "DEAFNESS, CONDUCTIVE", "conduction; deafness", "Deafness, conductive", "DEAFNESS, TRANSMISSION", "conductive loss hearing", "conductive hearing loss", "Conductive deafness NOS", "Conductive Hearing Loss", "Conductive hearing loss", "Hearing loss, conductive", "CD - Conductive deafness", "Conductive deafness, NOS", "Hearing Loss, Conductive", "HEARING DISORDER, CONDUCTIVE", "Conductive hearing loss, NOS", "Conductive hearing impairment", "CHL - Conductive hearing loss", "Hearing impairment, conductive", "conductive hearing loss disorder", "Conductive hearing loss (disorder)", "loss; hearing, conductive disorder", "hearing; loss, conductive disorder", "conductive hearing loss (diagnosis)", "Conductive hearing loss, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "conductive hearing loss disorder", "shortest_name_length": 19}
{"curie": "MONDO:0032655", "names": ["VIPB", "VISUAL IMPAIRMENT AND PROGRESSIVE PHTHISIS BULBI", "visual impairment and progressive phthisis bulbi"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "visual impairment and progressive phthisis bulbi", "shortest_name_length": 4}
{"curie": "UMLS:C0457531", "names": ["Acanthomatous Ameloblastoma", "Acanthomatous ameloblastoma", "Acanthomatous ameloblastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acanthomatous ameloblastoma", "shortest_name_length": 27}
{"curie": "UMLS:C0750901", "names": ["early onset; Alzheimer", "Alzheimer; early onset", "Presenile Alzheimer Dementia", "presenile alzheimer dementia", "Alzheimer disease early onset", "Early Onset Alzheimer Disease", "alzheimer disease early onset", "Alzheimer Disease, Early Onset", "alzheimers disease early onset", "Alzheimer disease, early-onset", "alzheimer's disease early onset", "Early onset Alzheimer's disease", "early onset alzheimer's disease", "Presenile dementia, Alzheimer's type", "Alzheimer's disease with early onset", "Dementia in Alzheimer's disease - type 2", "Alzheimer disease early onset (diagnosis)", "dementia of Alzheimer's type with early onset", "Dementia of the Alzheimers type with early onset", "Dementia in Alzheimer's disease with early onset", "dementia; presenile, Alzheimer's type (manifestation)", "dementia of Alzheimer's type with early onset (diagnosis)", "Primary degenerative dementia of the Alzheimer type, early onset", "Primary degenerative dementia of the Alzheimer type, presenile onset", "Primary degenerative dementia of the Alzheimer type, presenile onset (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alzheimer Disease, Early Onset", "shortest_name_length": 22}
{"curie": "UMLS:C5556805", "names": ["Recurrent Primary Cutaneous Anaplastic Large Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Primary Cutaneous Anaplastic Large Cell Lymphoma", "shortest_name_length": 58}
{"curie": "MONDO:0044797", "names": ["Desmoplastic Nevus", "desmoplastic nevus", "Desmoplastic nevus of skin", "Desmoplastic naevus of skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "desmoplastic nevus", "shortest_name_length": 18}
{"curie": "MONDO:0024320", "names": ["Inner ear tumor", "Inner ear tumour", "inner Ear neoplasm", "internal ear tumor", "Inner Ear Neoplasm", "inner ear neoplasm", "internal Ear neoplasm", "tumor of internal ear", "internal ear neoplasm", "Internal Ear Neoplasm", "neoplasm of internal ear", "Neoplasm of the inner ear", "internal ear neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inner ear neoplasm", "shortest_name_length": 15}
{"curie": "UMLS:C1336240", "names": ["Stage III AIDS-Related Anal Canal Cancer", "Stage III AIDS-Related Anal Canal Cancer AJCC v6", "Stage III AIDS-Related Anal Canal Cancer AJCC v7", "Stage III AIDS-Related Anal Carcinoma AJCC v6 and v7", "Stage III AIDS-Related Anal Canal Cancer AJCC v6 and v7", "Stage III AIDS-Related Anal Canal Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III AIDS-Related Anal Canal Cancer AJCC v6 and v7", "shortest_name_length": 40}
{"curie": "MONDO:0005166", "names": ["Osteoma", "OSTEOMA", "osteoma", "Osteomas", "osteomas", "Osteoma NOS", "Osteoma, NOS", "Benign osteoma", "OSTEOMA, BENIGN", "osteoma, benign", "osteoma (disease)", "benign osteoma of bone", "benign osteoma of bone (diagnosis)", "Benign osteoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteoma", "shortest_name_length": 7}
{"curie": "UMLS:C4521750", "names": ["IVB", "Stage IVB Esophageal Squamous Cell Cancer", "Pathologic Stage IVB Esophageal Squamous Cell Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IVB Esophageal Squamous Cell Carcinoma AJCC v8", "shortest_name_length": 3}
{"curie": "UMLS:C0554309", "names": ["azotemia", "azotaemia", "Blum's syndrome", "Prerenal uremia", "prerenal; uremia", "uremia; prerenal", "Prerenal uraemia", "PRERENAL AZOTEMIA", "azotemia prerenal", "Prerenal azotemia", "prerenal azotemia", "Azotemia prerenal", "AZOTEMIA PRERENAL", "Prerenal azotaemia", "Azotaemia prerenal", "RENAL FAILURE PRERENAL", "Prerenal renal failure", "Prerenal uremia syndrome", "Prerenal uraemia syndrome", "Extrarenal uremia syndrome", "Extrarenal uraemia syndrome", "RENAL INSUFFICIENCY PRERENAL", "Prerenal azotemia (disorder)", "prerenal azotemia (diagnosis)", "Azotemia due to inadequate renal perfusion", "Azotaemia due to inadequate renal perfusion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prerenal azotemia", "shortest_name_length": 8}
{"curie": "MONDO:0002595", "names": ["Vaccinia", "VACCINIA", "vaccinia", "Vaccinias", "Vaccinia, NOS", "Vaccinia (disorder)", "vaccinia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vaccinia", "shortest_name_length": 8}
{"curie": "UMLS:C2729139", "names": ["Immune-mediated myositis", "immune-mediated myositis", "immune inflammatory myopathy", "immune inflammatory myopathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immune-mediated myositis", "shortest_name_length": 24}
{"curie": "UMLS:C1378105", "names": ["fallopian tube cancer stage II", "stage II fallopian tube cancer", "Stage II Fallopian Tube Cancer", "Fallopian Tube Cancer Stage II", "AJCC stage II fallopian tube cancer", "AJCC Stage II Fallopian Tube Cancer", "stage II fallopian tube cancer AJCC v6", "stage II fallopian tube cancer AJCC v7", "Stage II Fallopian Tube Cancer AJCC v6", "FIGO stage II fallopian tube carcinoma", "FIGO Stage II Fallopian Tube Carcinoma", "Stage II Fallopian Tube Cancer AJCC v7", "FIGO stage II carcinoma of fallopian tube", "FIGO Stage II Carcinoma of Fallopian Tube", "FIGO stage II carcinoma of the fallopian tube", "Stage II Fallopian Tube Cancer AJCC v6 and v7", "FIGO Stage II Carcinoma of the Fallopian Tube"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Fallopian Tube Cancer", "shortest_name_length": 30}
{"curie": "MONDO:0000961", "names": ["Endobronchial Lipoma", "Endobronchial lipoma", "endobronchial lipoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endobronchial lipoma", "shortest_name_length": 20}
{"curie": "UMLS:C0278497", "names": ["Stomach cancer stage III", "Gastric cancer stage III", "Stage III Gastric Cancer", "stage III gastric cancer", "gastric cancer, stage III", "stomach cancer, stage III", "Gastric malignancy stage III", "Stage III Gastric Cancer AJCC v7", "Stage III Gastric (Stomach) Cancer", "Malignant neoplasm of stomach stage III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant neoplasm of stomach stage III", "shortest_name_length": 24}
{"curie": "UMLS:C4687709", "names": ["Recurrent Medulloblastoma, SHH-Activated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Medulloblastoma, SHH-Activated", "shortest_name_length": 40}
{"curie": "UMLS:C0031144", "names": ["chronic peritoneal effusion", "Chronic peritoneal effusion", "Chronic Peritoneal Effusion", "Peritoneal effusion (chronic)", "Chronic peritoneal effusion (disorder)", "chronic peritoneal effusion (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic peritoneal effusion (disorder)", "shortest_name_length": 27}
{"curie": "UMLS:C0234934", "names": ["Urticaria bullosa", "Bullous urticaria", "Vesicular urticaria", "URTICARIA VESICULOSA", "Urticaria vesiculosa", "Bullous urticaria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bullous urticaria", "shortest_name_length": 17}
{"curie": "MONDO:0010100", "names": ["tsd", "TSD", "Sachs", "Tay-Sachs", "Sachs-Tay", "HEXA DEFICIENCY", "hexa deficiency", "disease sach tay", "disease tay sach", "TAY SACHS DISEASE", "tay-sachs disease", "Tay-Sachs Disease", "Tay-Sachs disease", "disease sachs tay", "TAY-SACHS DISEASE", "TAY-Sachs disease", "disease tay-sachs", "disease tay sachs", "Tay Sachs disease", "Tay Sachs Disease", "tay sachs disease", "GM2 gangliosidosis", "disease sach's tay", "diseases tay sachs", "tay sach's disease", "TAY SACH'S DISEASE", "disease, Tay-Sachs", "diseases sachs tay", "Disease, Tay-Sachs", "diseases sachs tays", "Hex A pseudodeficiency", "deficiency hexosaminidase", "Amaurotic familial idiocy", "Type I GM2-Gangliosidosis", "Amaurotic Familial Idiocy", "amaurotic familial idiocy", "gangliosidosis GM2 type I", "GANGLIOSIDOSIS GM2 TYPE 1", "Familial Amaurotic Idiocy", "GM2 gangliosidosis, type I", "GM2-Gangliosidosis, Type I", "Amaurotic Idiocy, Familial", "Gangliosidosis GM2, Type I", "GM2-gangliosidosis, type 1", "gangliosidosis GM2, type 1", "GM2 gangliosidosis, type 1", "GM2-GANGLIOSIDOSIS, TYPE I", "Tay-Sachs Sphingolipidosis", "GM2 Gangliosidosis, Type I", "GM2 Gangliosidosis, Type 1", "Familial Idiocy (Amaurotic)", "hexosaminidase a deficiency", "Tay-Sachs Disease, Juvenile", "Tay-Sachs disease, juvenile", "Sphingolipidosis, Tay Sachs", "TAY-SACHS DISEASE, JUVENILE", "Gangliosidosis GM2 , Type 1", "Sphingolipidosis, Tay-Sachs", "sphingolipidosis, Tay-Sachs", "hexosaminidase A deficiency", "Hexosaminidase A deficiency", "HEXOSAMINIDASE A DEFICIENCY", "B Variant GM2-Gangliosidoses", "G(M2) Gangliosidosis, Type I", "B Variant GM2-Gangliosidosis", "B VARIANT GM2-GANGLIOSIDOSIS", "Tay Sachs Disease, B Variant", "Gangliosidosis G(M2), Type I", "GM>2< gangliosidosis, type 1", "B Variant GM2 Gangliosidosis", "B variant GM2 gangliosidosis", "Tay-Sachs Disease, B Variant", "Tay-Sachs disease (disorder)", "B variant GM2-gangliosidosis", "Tay-Sachs Disease, Variant B1", "Tay-Sachs disease, variant B1", "Gangliosidosis GM2, B Variant", "GM2 Gangliosidosis, B Variant", "TAY-SACHS DISEASE, VARIANT B1", "GM2-Gangliosidosis, B Variant", "Tay-Sachs disease, B1 variant", "Tay-Sachs disease (diagnosis)", "TAY-SACHS DISEASE, B1 VARIANT", "GM2-GANGLIOSIDOSIS, VARIANT B1", "GM2-gangliosidosis, variant B1", "GM2 gangliosidosis, B1 variant", "Gm2-Gangliosidosis, Variant B1", "GM2-GANGLIOSIDOSIS, B1 VARIANT", "INFANTILE GANGLIOSIDE LIPIDOSIS", "GM2 gangliosidosis, B, B1 variant", "GM2-gangliosidosis, several forms", "LIPIDOSIS, GANGLIOSIDE, INFANTILE", "Severe hexosaminidase A deficiency", "Hexosaminidase A Deficiency Disease", "Deficiency Disease Hexosaminidase A", "INFANTILE AMAUROTIC FAMILIAL IDIOCY", "Infantile amaurotic familial disease", "Tay-Sachs disease, pseudo-Ab variant", "Tay-Sachs Disease, Pseudo-AB Variant", "TAY-SACHS DISEASE, PSEUDO-AB VARIANT", "GM<sub>2</sub> gangliosidosis, type 1", "B1 variant hexosaminidase A deficiency", "GM2-gangliosidosis, adult chronic type", "GM2-GANGLIOSIDOSIS, ADULT CHRONIC TYPE", "Gm2-Gangliosidosis, Adult Chronic Type", "Hexosaminidase A deficiency, B1 variant", "hexosaminidase a deficiency, adult type", "B1 variant hexosaminidase A deficiency (disorder)", "hexosaminidase alpha-subunit deficiency (variant B)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tay-Sachs disease", "shortest_name_length": 3}
{"curie": "UMLS:C3896964", "names": ["Long-Term Effects Secondary to Cancer Therapy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Long-Term Effects Secondary to Cancer Therapy", "shortest_name_length": 45}
{"curie": "MONDO:0007860", "names": ["Keratosis focal palmoplantar gingival", "keratosis focal palmoplantar gingival", "keratosis, focal palmoplantar and gingival", "Keratosis, Focal Palmoplantar and Gingival", "KERATOSIS, FOCAL PALMOPLANTAR AND GINGIVAL", "Focal palmoplantar and gingival keratoderma", "focal palmoplantar and gingival keratoderma", "focal palmoplantar and gingival hyperkeratosis", "Focal palmoplantar and gingival hyperkeratosis", "Focal palmoplantar and oral mucosa hyperkeratosis", "focal palmoplantar and oral mucosa hyperkeratosis", "Focal palmoplantar and gingival keratoderma (disorder)", "Focal Palmoplantar and Gingival Hyperkeratosis Syndrome", "FOCAL PALMOPLANTAR AND GINGIVAL HYPERKERATOSIS SYNDROME", "focal palmoplantar and gingival hyperkeratosis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal palmoplantar and gingival keratoderma", "shortest_name_length": 37}
{"curie": "UMLS:C0263268", "names": ["Dermatitis due to dichromate", "Dermatitis due to Dichromate", "contact dermatitis due to dichromate", "Contact dermatitis due to dichromate", "Contact dermatitis caused by dichromate", "contact dermatitis due to dichromate (diagnosis)", "Contact dermatitis caused by dichromate (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Contact dermatitis due to dichromate", "shortest_name_length": 28}
{"curie": "MONDO:0002436", "names": ["nose disease", "Nose Disease", "disease nose", "nose disorder", "diseases nose", "Disease, Nose", "Nose Diseases", "Nasal Disease", "nose diseases", "nose; disorder", "Diseases, Nose", "Nose--Diseases", "disorders nose", "nasal disorder", "Nasal Diseases", "Nasal disorder", "Nasal Disorder", "Disease, Nasal", "Disorder, Nasal", "disorders nasal", "Nasal disorders", "Nasal Disorders", "Diseases, Nasal", "disease of nose", "Disorders, Nasal", "disorder of nose", "Nasal disorder NOS", "disease of the nose", "Disorder of the nose", "disorder of the nose", "nose disease or disorder", "Disease of the nose, NOS", "disease (or disorder); nose", "Disease or syndrome of nose", "disease or disorder of nose", "disorder of nose (diagnosis)", "Disorder of the nose (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasal disorder", "shortest_name_length": 12}
{"curie": "MONDO:0005117", "names": ["Aeromonas hydrophila infectious disease", "Aeromonas hydrophila disease or disorder", "Aeromonas hydrophila caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aeromonas hydrophila infectious disease", "shortest_name_length": 39}
{"curie": "MONDO:0020823", "names": ["Infantile miliaria", "infantile miliaria", "Infantile miliaria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile miliaria", "shortest_name_length": 18}
{"curie": "MONDO:0014225", "names": ["HFE5", "hemochromatosis type 5", "hemochromatosis, type 5", "HEMOCHROMATOSIS, TYPE 5", "FTH1-related iron overload", "FTH1-associated iron overload", "FTH1 hereditary hemochromatosis", "IRON OVERLOAD, AUTOSOMAL DOMINANT", "iron overload, autosomal dominant", "Iron Overload, Autosomal Dominant", "Ferritin heavy chain 1-related iron overload", "FTH1 (ferritin heavy chain 1) related iron overload", "hereditary hemochromatosis caused by mutation in FTH1", "Ferritin heavy chain 1-related iron overload (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemochromatosis type 5", "shortest_name_length": 4}
{"curie": "UMLS:C0333704", "names": ["Chromosome break", "Chromosome Break", "Chromosomal Break", "Chromosome Breaks", "Break, Chromosome", "Chromosomal Breaks", "Break, Chromosomal", "Breaks, Chromosome", "Breaks, Chromosomal", "Chromosome break (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chromosome Breaks", "shortest_name_length": 16}
{"curie": "UMLS:C3544231", "names": ["Hyponatremic seizure", "Hyponatraemic seizure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyponatraemic seizure", "shortest_name_length": 20}
{"curie": "MONDO:0005838", "names": ["Mansonelloses", "Mansonellosis", "mansonelliasis", "Mansonelliases", "Mansonelliasis", "Mansonelliasis (disorder)", "mansonelliasis (diagnosis)", "Mansonella perstans infections"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mansonelliasis", "shortest_name_length": 13}
{"curie": "MONDO:0004249", "names": ["supratentorial ependymoma", "Supratentorial Ependymoma", "pediatric cerebral ependymoma", "pediatric Cerebral Ependymoma", "paediatric Cerebral Ependymoma", "childhood supratentorial ependymoma", "Childhood Supratentorial Ependymoma", "pediatric supratentorial ependymoma", "ependymoma, pediatric supratentorial", "supratentorial ependymoma, childhood", "ependymoma, childhood supratentorial", "paediatric supratentorial ependymoma", "Childhood Supratentorial Ependymoma, NOS", "childhood supratentorial ependymoblastoma", "pediatric Supratentorial Ependymoblastoma", "pediatric supratentorial ependymoblastoma", "supratentorial ependymoblastoma, childhood", "ependymoblastoma, childhood supratentorial", "paediatric Supratentorial Ependymoblastoma", "pediatric CNS tumor supratentorial ependymoma", "CNS tumor, pediatric supratentorial ependymoma", "CNS tumor, childhood supratentorial ependymoma", "childhood CNS tumor, supratentorial ependymoma", "childhood brain tumor, supratentorial ependymoma", "brain tumor, childhood supratentorial ependymoma", "brain tumor, pediatric supratentorial ependymoma", "pediatric brain tumor, supratentorial ependymoma", "brain tumor, supratentorial ependymoma, childhood", "Childhood Supratentorial Ependymoma, Not Otherwise Specified", "central nervous system tumor, supratentorial ependymoma, childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pediatric supratentorial ependymoma", "shortest_name_length": 25}
{"curie": "UMLS:C4763783", "names": ["Recurrent Primary Effusion Lymphoma", "Recurrent HHV8-Positive Primary Effusion Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Primary Effusion Lymphoma", "shortest_name_length": 35}
{"curie": "UMLS:C5552921", "names": ["G6PC3 Deficiency", "Glucose-6-Phosphatase 3 Deficiency", "Glucose-6-phosphatase Catalytic Subunit 3 Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Glucose-6-Phosphatase 3 Deficiency", "shortest_name_length": 16}
{"curie": "UMLS:C0855158", "names": ["Stage IV Primary Mediastinal Large B-Cell Lymphoma", "Primary Mediastinal Large B-Cell Lymphoma Stage IV", "Primary mediastinal large B-cell lymphoma stage IV", "Stage IV Mediastinal (Thymic) Large B-Cell Lymphoma", "Ann Arbor Stage IV Primary Mediastinal (Thymic) Large B-Cell Lymphoma", "Large B-cell lymphoma subtype primary mediastinal (Thymic) large B-cell lymphoma stage IV"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary mediastinal large B-cell lymphoma stage IV", "shortest_name_length": 50}
{"curie": "MONDO:0013044", "names": ["AHUS6", "AHUS, SUSCEPTIBILITY TO, 6", "Ahus, susceptibility to, 6", "aHUS with thrombomodulin anomaly", "D-HUS with thrombomodulin anomaly", "atypical HUS with thrombomodulin anomaly", "susceptibility to atypical hemolytic uremic syndrome 6", "hemolytic uremic syndrome, atypical, susceptibility to, 6", "HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 6", "hemolytic uremic syndrome, atypical, susceptibility to, type 6", "atypical hemolytic-uremic syndrome with thrombomodulin anomaly", "hemolytic-uremic syndrome without diarrhea with thrombomodulin anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical hemolytic-uremic syndrome with thrombomodulin anomaly", "shortest_name_length": 5}
{"curie": "MONDO:0014752", "names": ["NPHS11", "nephrotic syndrome type 11", "nephrotic syndrome, type 11", "NEPHROTIC SYNDROME, TYPE 11", "Nup107 familial nephrotic syndrome", "NUP107 familial nephrotic syndrome", "nephrotic syndrome, type 11; NPHS11", "familial nephrotic syndrome caused by mutation in NUP107", "familial nephrotic syndrome caused by mutation in Nup107"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrotic syndrome, type 11", "shortest_name_length": 6}
{"curie": "MONDO:0005583", "names": ["disease animal", "animal disease", "Animal Diseases", "animal diseases", "animals disease", "Diseases, Animal", "diseases, animal", "animals diseases", "Animals--Diseases", "non-human animal disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-human animal disease", "shortest_name_length": 14}
{"curie": "UMLS:C4725926", "names": ["Tumors Derived from Langerhans Cells"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tumors Derived from Langerhans Cells", "shortest_name_length": 36}
{"curie": "MONDO:0002042", "names": ["mechanical ectropion", "Mechanical ectropion", "Mechanical ectropion (disorder)", "mechanical ectropion (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mechanical ectropion", "shortest_name_length": 20}
{"curie": "MONDO:0009114", "names": ["CSID", "SI deficiency", "Si Deficiency", "SI DEFICIENCY", "Invertase deficiency", "invertase deficiency", "isomaltase deficiency", "Deficiency of invertase", "deficiency of isomaltase", "Deficiency of saccharase", "Deficiency of isomaltase", "Disaccharide intolerance", "disaccharide intolerance", "Disaccharide intolerance I", "disaccharide intolerance 1", "Disaccharide Intolerance 1", "Disaccharide Intolerance I", "DISACCHARIDE INTOLERANCE I", "disaccharide intolerance i", "disaccharide intolerance, 1", "Disaccharide intolerance, 1", "Sucrase-Isomaltase Deficiency", "Sucrase-isomaltase deficiency", "sucrase-isomaltase deficiency", "sucrase isomaltase deficiency", "Congenital Sucrose Intolerance", "Congenital sucrose intolerance", "congenital sucrose intolerance", "Sucrose intolerance congenital", "sucrose intolerance congenital", "sucrose intolerance, congenital", "SUCROSE INTOLERANCE, CONGENITAL", "Sucrose Intolerance, Congenital", "Congenital sucrose malabsorption", "congenital sucrose malabsorption", "Deficiency of oligo-1,6-glucosidase", "sucrase alpha dextrinase deficiency", "Deficiency of isomaltase (disorder)", "Sucrase-alpha-dextrinase deficiency", "sucrase-alpha-dextrinase deficiency", "sucrose isomaltose enzyme deficiency", "Deficiency of beta-fructofuranosidase", "Congenital sucrase-isomaltase deficiency", "genetic sucrase-isomaltose malabsorption", "Sucrase-isomaltase deficiency (disorder)", "Congenital Sucrase-Isomaltase Deficiency", "congenital sucrase-isomaltase deficiency", "Sucrase-isomaltase deficiency (diagnosis)", "Congenital sucrose-isomaltase intolerance", "sucrase-isomaltase deficiency, congenital", "congenital sucrose-isomaltase intolerance", "SUCRASE-ISOMALTASE DEFICIENCY, CONGENITAL", "Disaccharide intolerance syndrome, type I", "Sucrase-isomaltase deficiency, congenital", "Intestinal sucrase-a-dextrinase deficiency", "intestinal sucrase-a-dextrinase deficiency", "Congenital Sucrose-Isomaltose Malabsorption", "congenital sucrose-isomaltase malabsorption", "Congenital sucrose-isomaltase malabsorption", "congenital sucrase-isomaltose malabsorption", "congenital sucrose isomaltose malabsorption", "Sucrose-isomaltase malabsorption, congenital", "SUCROSE-ISOMALTOSE MALABSORPTION, CONGENITAL", "sucrose-isomaltose malabsorption, congenital", "Sucrose-Isomaltose Malabsorption, Congenital", "sucrose-isomaltase malabsorption, congenital", "Deficiency of beta-fructofuranosidase (disorder)", "intestinal disaccharidase deficiency sucrase-isomaltase"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital sucrase-isomaltase deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0020651", "names": ["mixed germ cell tumor of vulva"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed germ cell tumor of vulva", "shortest_name_length": 30}
{"curie": "MONDO:0008462", "names": ["split lower lip", "SPLIT LOWER LIP", "split Lower type lip"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "split lower lip", "shortest_name_length": 15}
{"curie": "UMLS:C1335519", "names": ["Prostate Carcinosarcoma", "Prostate Sarcomatoid Carcinoma", "Sarcomatoid Carcinoma of Prostate", "Sarcomatoid Carcinoma of the Prostate", "Prostate Acinar Adenocarcinoma, Sarcomatoid Variant", "Acinar Prostate Adenocarcinoma, Sarcomatoid Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Acinar Adenocarcinoma, Sarcomatoid Variant", "shortest_name_length": 23}
{"curie": "MONDO:0004216", "names": ["germinoma", "pineal germinoma", "Pineal germinoma", "Pineal Germinoma", "Pineal Region Germinoma", "pineal region germinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pineal region germinoma", "shortest_name_length": 9}
{"curie": "UMLS:C1333297", "names": ["Type C LyP", "Diffuse Large Cell Type LyP", "Type C Lymphomatoid Papulosis", "lymphomatoid papulosis, type C", "lymphomatoid papulosis, type C (diagnosis)", "Diffuse Large Cell Type Lymphomatoid Papulosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphomatoid papulosis, type C", "shortest_name_length": 10}
{"curie": "MONDO:0005651", "names": ["arenaviral hemorrhagic fever", "arenavirus hemorrhagic fever", "Arenavirus hemorrhagic fever", "Hemorrhagic fever arenaviral", "Arenaviral hemorrhagic fever", "hemorrhagic fever; arenaviral", "Haemorrhagic fever arenaviral", "arenaviral; hemorrhagic fever", "Arenaviral haemorrhagic fever", "fever; hemorrhagic, arenaviral", "Hemorrhagic fever arenaviral NOS", "Haemorrhagic fever arenaviral NOS", "Arenaviral hemorrhagic fever, NOS", "Arenaviral haemorrhagic fever, NOS", "arenavirus infection hemorrhagic fever", "Arenaviral hemorrhagic fever (disorder)", "Arenaviral hemorrhagic fever (diagnosis)", "Arenaviral hemorrhagic fever, unspecified", "Arenaviral haemorrhagic fever, unspecified", "infection; viral, hemorrhagic fever, arenaviral", "infection; viral, arenaviral, hemorrhagic fever"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arenavirus hemorrhagic fever", "shortest_name_length": 28}
{"curie": "UMLS:C1510691", "names": ["AIDS-Related Lymphoma by Working Formulation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Lymphoma by Working Formulation", "shortest_name_length": 44}
{"curie": "MONDO:0100037", "names": ["juvenile onset PRP", "juvenile onset pityriasis rubra pilaris"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile onset pityriasis rubra pilaris", "shortest_name_length": 18}
{"curie": "UMLS:C1332061", "names": ["AIDS-Related Toxoplasmosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Toxoplasmosis", "shortest_name_length": 26}
{"curie": "MONDO:0025431", "names": ["infectious keratoconjunctivitis", "Infectious Keratoconjunctivitis", "Keratoconjunctivitis, Infectious", "keratoconjunctivitis, infectious", "infectious Keratoconjunctivitides", "Infectious Keratoconjunctivitides", "Keratoconjunctivitides, infectious", "Keratoconjunctivitides, Infectious", "infectious; keratoconjunctivitis (etiology)", "keratoconjunctivitis; infectious (etiology)", "infectious; keratoconjunctivitis (manifestation)", "keratoconjunctivitis; infectious (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratoconjunctivitis, infectious", "shortest_name_length": 31}
{"curie": "UMLS:C4055018", "names": ["Familial Atypical Hemolytic Uremic Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Familial Atypical Hemolytic Uremic Syndrome", "shortest_name_length": 43}
{"curie": "MONDO:0013879", "names": ["PFBMFT2", "aplastic anemia", "pulmonary fibrosis, idiopathic, susceptibility to", "pulmonary fibrosis and/or bone marrow failure, TELOMERE-RELATED, 2", "PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 2", "pulmonary fibrosis and/or bone marrow failure, Telomere-related, 2", "pulmonary fibrosis and/or bone marrow failure, Telomere-related, type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary fibrosis and/or bone marrow failure, Telomere-related, 2", "shortest_name_length": 7}
{"curie": "UMLS:C3549742", "names": ["Breast cancer, lobular"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast cancer, lobular", "shortest_name_length": 22}
{"curie": "UMLS:C4727841", "names": ["Recurrent Pancreatic Acinar Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Pancreatic Acinar Cell Carcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0060550", "names": ["PAPA7", "polydactyly, postaxial, type A7", "polydactyly, postaxial, type a7", "POLYDACTYLY, POSTAXIAL, TYPE A7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polydactyly, postaxial, type a7", "shortest_name_length": 5}
{"curie": "UMLS:C1334652", "names": ["Mediastinal Embryonal Carcinoma", "Embryonal Carcinoma of Mediastinum", "embryonal carcinoma of mediastinum", "Embryonal Carcinoma of the Mediastinum", "embryonal carcinoma of mediastinum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "embryonal carcinoma of mediastinum", "shortest_name_length": 31}
{"curie": "MONDO:0009916", "names": ["17-KSR deficiency", "17-Ksr Deficiency", "17-KSR DEFICIENCY", "17B-HSD deficiency", "17 beta HSD3 Deficiency", "17 Beta HSD3 Deficiency", "17 alpha KSR deficiency", "17 Beta HSD3 deficiency", "17 beta HSD3 deficiency", "17-ketoreductase deficiency", "17-ketosteroidreductase deficiency", "17-ketosteroid reductase deficiency", "17-Ketosteroid reductase deficiency", "17-Hydroxysteroid Dehydrogenase Deficiency", "male pseudohermaphroditism with gynecomastia", "Male pseudohermaphroditism with gynecomastia", "17b-hydroxysteroid oxidoreductase deficiency", "17-ketosteroid reductase deficiency of testis", "Male pseudoherma-phroditism with gynecomastia", "Testosterone 17-beta-dehydrogenase deficiency", "17-Ketosteroid Reductase Deficiency Of Testis", "17-KETOSTEROID REDUCTASE DEFICIENCY OF TESTIS", "Pseudohermaphroditism, Male, with Gynecomastia", "PSEUDOHERMAPHRODITISM, MALE, WITH GYNECOMASTIA", "pseudohermaphroditism, Male, with gynecomastia", "17 Beta-hydroxysteroid dehydrogenase deficiency", "17-ketosteroid reductase deficiency (diagnosis)", "17 beta-hydroxysteroid oxidoreductase deficiency", "17-beta hydroxysteroid dehydrogenase 3 deficiency", "17-Beta hydroxysteroid dehydrogenase 3 deficiency", "17-Beta-Hydroxysteroid Dehydrogenase 3 Deficiency", "17-Beta Hydroxysteroid Dehydrogenase 3 Deficiency", "17-beta-hydroxysteroid dehydrogenase 3 deficiency", "17-BETA HYDROXYSTEROID DEHYDROGENASE III DEFICIENCY", "17-BETA hydroxysteroid dehydrogenase III deficiency", "17 alpha ketosteroid reductase deficiency of testis", "17 beta hydroxysteroid dehydrogenase III deficiency", "17-Beta Hydroxysteroid Dehydrogenase III Deficiency", "17-@BETA HYDROXYSTEROID DEHYDROGENASE III DEFICIENCY", "NEUTRAL 17-BETA-HYDROXYSTEROID OXIDOREDUCTASE DEFICIENCY", "neutral 17-beta-hydroxysteroid oxidoreductase deficiency", "neutral 17 beta hydroxysteroid oxidoreductase deficiency", "neutral 17-Beta-hydroxysteroid oxidoreductase deficiency", "Neutral 17-Beta-Hydroxysteroid Oxidoreductase Deficiency", "Neutral 17-beta-hydroxysteroid oxidoreductase deficiency", "Neutral 17 beta-hydroxysteroid oxidoreductase deficiency", "Testosterone 17-beta-dehydrogenase deficiency (disorder)", "17 beta-hydroxysteroid oxidoreductase deficiency (diagnosis)", "polycystic ovary syndrome due to 17-ketosteroid reductase deficiency", "POLYCYSTIC OVARY SYNDROME DUE TO 17-KETOSTEROID REDUCTASE DEFICIENCY", "Polycystic Ovarian Disease due to 17-Ketosteroid Reductase Deficiency", "polycystic ovarian disease due to 17-ketosteroid reductase deficiency", "Male pseudohermaphroditism due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency", "46,XY disorder of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XY disorder of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency", "shortest_name_length": 17}
{"curie": "MONDO:0060663", "names": ["CHTD5", "CONGENITAL heart defects, multiple types, 5", "CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 5", "congenital heart defects, multiple types, 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital heart defects, multiple types, 5", "shortest_name_length": 5}
{"curie": "MONDO:0004483", "names": ["OAT", "Hurthle Cell Adenoma", "Hurthle cell adenoma", "Thyroid Oncocytic Adenoma", "thyroid oncocytic adenoma", "Benign Thyroid Oncocytoma", "benign thyroid oncocytoma", "benign oncocytoma of thyroid", "Benign Oncocytoma of Thyroid", "Oncocytic Adenoma of Thyroid", "thyroid Hurthle cell adenoma", "Thyroid Hurthle Cell Adenoma", "Hurthle cell thyroid adenoma", "oncocytic adenoma of thyroid", "Hurthle cell adenoma of thyroid", "Hurthle Cell Adenoma of Thyroid", "Benign Thyroid Gland Oncocytoma", "thyroid gland oncocytic adenoma", "Thyroid Gland Oncocytic Adenoma", "benign thyroid gland oncocytoma", "Benign Oncocytoma of the Thyroid", "Oncocytic Adenoma of the Thyroid", "oncocytic adenoma of the thyroid", "benign oncocytoma of the thyroid", "Oncocytic Adenoma of Thyroid Gland", "benign oncocytoma of thyroid gland", "Benign Oncocytoma of Thyroid Gland", "Thyroid Gland Hurthle Cell Adenoma", "oncocytic adenoma of thyroid gland", "thyroid gland Hurthle cell adenoma", "Hurthle cell adenoma of the thyroid", "Hurthle Cell Adenoma of the Thyroid", "Hurthle Cell Adenoma of Thyroid Gland", "Hurthle cell adenoma of thyroid gland", "oncocytic adenoma of the thyroid gland", "Oncocytic Adenoma of the Thyroid Gland", "Benign Oncocytoma of the Thyroid Gland", "benign oncocytoma of the thyroid gland", "Hurthle cell adenoma of the thyroid gland", "Hurthle Cell Adenoma of the Thyroid Gland", "Thyroid Follicular Adenoma of Oxyphilic Cell Type", "thyroid follicular adenoma of oxyphilic cell type", "Follicular Adenoma of Thyroid of Oxyphilic Cell Type", "follicular adenoma of thyroid of oxyphilic cell type", "Thyroid Follicular Adenoma of the Oxyphilic Cell Type", "thyroid follicular adenoma of the oxyphilic cell type", "Thyroid Gland Follicular Adenoma of Oxyphilic Cell Type", "thyroid gland follicular adenoma of oxyphilic cell type", "Follicular Adenoma of Thyroid Gland of Oxyphilic Cell Type", "follicular adenoma of thyroid gland of oxyphilic cell type", "Thyroid Gland Follicular Adenoma of the Oxyphilic Cell Type", "thyroid gland follicular adenoma of the oxyphilic cell type", "Follicular Adenoma of the Thyroid of the Oxyphilic Cell Type", "follicular adenoma of the thyroid of the oxyphilic cell type", "Follicular Adenoma of the Thyroid Gland of the Oxyphilic Cell Type", "follicular adenoma of the thyroid gland of the oxyphilic cell type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid gland oncocytic adenoma", "shortest_name_length": 3}
{"curie": "UMLS:C4763628", "names": ["Metastatic Squamous Cell Carcinoma in Cervical Lymph Node", "Metastatic Squamous Cell Carcinoma in the Cervical Lymph Nodes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Squamous Cell Carcinoma in the Cervical Lymph Nodes", "shortest_name_length": 57}
{"curie": "UMLS:C0751172", "names": ["Adult Glycogen Storage Disease Type II", "Glycogen Storage Disease Type II, Adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Glycogen Storage Disease Type II", "shortest_name_length": 38}
{"curie": "UMLS:C0854841", "names": ["Angioimmunoblastic T-Cell Lymphoma Stage III", "Stage III Angioimmunoblastic T-Cell Lymphoma", "Angioimmunoblastic T-cell lymphoma stage III", "Ann Arbor Stage III Angioimmunoblastic T-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Angioimmunoblastic T-cell lymphoma stage III", "shortest_name_length": 44}
{"curie": "MONDO:0030895", "names": ["NPHS22", "nephrotic syndrome type 22", "NEPHROTIC SYNDROME, TYPE 22", "nephrotic syndrome, type 22"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrotic syndrome, type 22", "shortest_name_length": 6}
{"curie": "UMLS:C0262538", "names": ["tear ligament", "LIGAMENT TEAR", "Ligament tear", "ligament tear", "Tear;ligament", "ligament tears", "tear; ligament", "ligament; tear", "ligaments tears", "Ligament rupture", "ligament rupture", "ligaments tearing", "ligament; rupture", "rupture; ligament", "complete tear ligament", "Complete tear of ligament", "Ligament rupture (disorder)", "ligament rupture (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ligament rupture", "shortest_name_length": 13}
{"curie": "UMLS:C4528636", "names": ["Stage IV Acral Lentiginous Melanoma", "Stage IV Acral Melanoma AJCC v6 and v7", "Stage IV Acral Lentiginous Melanoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Acral Lentiginous Melanoma AJCC v6 and v7", "shortest_name_length": 35}
{"curie": "MONDO:0023230", "names": ["Ghose Sachdev Kumar syndrome", "Ghose-Sachdev-Kumar syndrome", "bilateral nanophthalmos, pigmentary retinal dystrophy, and angle closure glaucoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ghose-Sachdev-Kumar syndrome", "shortest_name_length": 28}
{"curie": "UMLS:C0343874", "names": ["Napkin candidosis", "Diaper candidosis", "Candida nappy rash", "Diaper candidiasis", "Candida Nappy Rash", "Napkin candidiasis", "Candidal nappy rash", "Monilial nappy rash", "Candida diaper rash", "Candida Diaper Rash", "Nappy rash monilial", "candida diaper rash", "Candidal diaper rash", "Candida Diaper Dermatitis", "Diaper candidiasis (disorder)", "neonatal candidiasis of diaper region", "neonatal candidiasis of diaper region (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diaper candidiasis", "shortest_name_length": 17}
{"curie": "MONDO:0030065", "names": ["ACOGS", "agenesis of corpus callosum, cardiac, ocular, and genital syndrome", "AGENESIS OF CORPUS CALLOSUM, CARDIAC, OCULAR, AND GENITAL SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "agenesis of corpus callosum, cardiac, ocular, and genital syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C5419779", "names": ["Ampulla of Vater Neuroendocrine Tumor G3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ampulla of Vater Neuroendocrine Tumor G3", "shortest_name_length": 40}
{"curie": "UMLS:C0268891", "names": ["Prostatic bleeding", "prostate; hemorrhage", "Prostatic hemorrhage", "hemorrhage; prostate", "Prostatic Hemorrhage", "Prostatic haemorrhage", "Hemorrhage of prostate", "hemorrhage of prostate", "Haemorrhage of prostate", "Hemorrhage of prostate (disorder)", "hemorrhage of prostate (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemorrhage of prostate", "shortest_name_length": 18}
{"curie": "MONDO:0020102", "names": ["Hereditary hydrocytosis", "hereditary stomatocytosis", "Hereditary stomatocytosis", "Stomatocytosis, congenital", "Hereditary stomatocytic disease", "hereditary stomatocytic disease", "hereditary hemolytic stomatocytosis", "Hereditary stomatocytosis (disorder)", "hereditary stomatocytosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary stomatocytosis", "shortest_name_length": 23}
{"curie": "MONDO:0014567", "names": ["MRT49", "NEDSPM", "MRT49, FORMERLY", "GPT2 deficiency", "mental retardation, autosomal recessive 49", "glutamate pyruvate transaminase 2 deficiency", "mental retardation, autosomal recessive type 49", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 49, FORMERLY", "neurodevelopmental disorder with microcephaly and spastic paraplegia", "NEURODEVELOPMENTAL DISORDER WITH SPASTIC PARAPLEGIA AND MICROCEPHALY", "postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glutamate pyruvate transaminase 2 deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0013513", "names": ["ATFB9", "atrial fibrillation familial 9", "ATRIAL FIBRILLATION, FAMILIAL, 9", "atrial fibrillation, familial, 9", "KCNJ2 familial atrial fibrillation", "atrial fibrillation, familial, type 9", "atrial fibrillation familial 9 (diagnosis)", "familial atrial fibrillation caused by mutation in KCNJ2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial fibrillation, familial, 9", "shortest_name_length": 5}
{"curie": "MONDO:0021058", "names": ["tumor syndrome", "Tumor Syndrome", "Neoplastic Syndrome", "neoplastic syndrome", "cancer-related syndrome", "Cancer-Related Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplastic syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C0854404", "names": ["injury iatrogenic", "Iatrogenic injury", "iatrogenic injury", "Iatrogenic injury NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Iatrogenic injury", "shortest_name_length": 17}
{"curie": "MONDO:0020435", "names": ["ASD coronary sinus", "Absent coronary sinus", "unroofed coronary sinus", "ASD, coronary sinus type", "Absence of coronary sinus", "atrial septal defect coronary sinus", "Congenital absence of coronary sinus", "coronary sinus atrial septal defects", "atrial septal defect, coronary sinus type", "Congenital absence of coronary sinus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial septal defect, coronary sinus type", "shortest_name_length": 18}
{"curie": "UMLS:C4054542", "names": ["Membranous Nephropathy - Autoimmune Disorder Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Membranous Nephropathy - Autoimmune Disorder Associated", "shortest_name_length": 55}
{"curie": "UMLS:C5235947", "names": ["Locally Advanced Malignant Peripheral Nerve Sheath Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Malignant Peripheral Nerve Sheath Tumor", "shortest_name_length": 56}
{"curie": "MONDO:0004460", "names": ["Fetal Adenoma", "fetal adenoma", "Fetal adenoma", "adenoma fetal", "Foetal adenoma", "thyroid fetal adenoma", "microfollicular adenoma", "Microfollicular adenoma", "Microfollicular Adenoma", "Thyroid Gland Fetal Adenoma", "thyroid gland fetal adenoma", "thyroid gland microfollicular adenoma", "Thyroid Gland Microfollicular Adenoma", "microfollicular adenoma (morphologic abnormality)", "Microfollicular adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid gland fetal adenoma", "shortest_name_length": 13}
{"curie": "UMLS:C2981252", "names": ["Stage IVB Sinonasal Cancer AJCC v7", "Stage IVB Sinonasal Carcinoma AJCC v7", "Stage IVB Nasal Cavity and Paranasal Sinus Cancer", "Stage IVB Nasal Cavity and Paranasal Sinus Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Nasal Cavity and Paranasal Sinus Cancer AJCC v7", "shortest_name_length": 34}
{"curie": "UMLS:C1707590", "names": ["Cutaneous Precursor Lymphoid Neoplasm", "Cutaneous Precursor Lymphoblastic Lymphoma/Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous Precursor Lymphoid Neoplasm", "shortest_name_length": 37}
{"curie": "MONDO:0012705", "names": ["ETL3", "FMTLE", "familial temporal lobe epilepsy 3", "EPILEPSY, FAMILIAL TEMPORAL LOBE, 3", "epilepsy, familial temporal lobe, 3", "familial mesial temporal lobe epilepsy", "familial temporal lobe epilepsy type 3", "EPILEPSY, FAMILIAL MESIAL TEMPORAL LOBE", "epilepsy, familial mesial temporal lobe", "Epilepsy, Familial Mesial Temporal Lobe"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial temporal lobe epilepsy 3", "shortest_name_length": 4}
{"curie": "MONDO:0013311", "names": ["EDSS", "EDSS1", "ectodermal dysplasia-syndactyly syndrome", "ectodermal dysplasia-syndactyly syndrome 1", "ectodermal dysplasia-syndactyly syndrome type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia-syndactyly syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0016611", "names": ["fetal lipoma", "Lipoblastoma", "Fetal Lipoma", "Fetal lipoma", "lipoblastoma", "Foetal lipoma", "lipoma; fetal", "lipoblastomas", "fetal; lipoma", "Lipoblastomas", "Infantile Lipoma", "infantile lipoma", "embryonic lipoma", "Embryonic Lipoma", "Fetal Lipomatosis", "Lipoblastomatosis", "Lipoblastomatoses", "Fetal lipoma, NOS", "Fetal lipomatosis", "Foetal lipoma, NOS", "Foetal lipomatosis", "Lipoblastoma (disorder)", "Lipoblastomatosis (disorder)", "Lipoblastoma/lipoblastomatosis", "Lipoblastoma AND/OR lipoblastomatosis", "Lipoblastoma/lipoblastomatosis (disorder)", "Lipoblastoma AND/OR lipoblastomatosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lipoblastoma", "shortest_name_length": 12}
{"curie": "MONDO:0006811", "names": ["intracranial hypotension", "Intracranial Hypotension", "Intracranial hypotension", "Hypotension, Intracranial", "hypotension; intracranial", "intracranial; hypotension", "Intracranial hypotension (disorder)", "intracranial hypotension (diagnosis)", "Intracranial hypotension, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intracranial hypotension", "shortest_name_length": 24}
{"curie": "UMLS:C1264047", "names": ["ABDOMEN LYMPHADENOPATHY", "Abdominal lymphadenopathy", "disorder of intra-abdominal lymph node", "Disorder of intra-abdominal lymph nodes", "Enlargement of intra-abdominal lymph node", "Disorder of intra-abdominal lymph nodes (disorder)", "disorder of intra-abdominal lymph node (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disorder of intra-abdominal lymph nodes", "shortest_name_length": 23}
{"curie": "MONDO:0002999", "names": ["Germinoma", "CNS germinoma", "Germinoma of CNS", "germinoma of CNS", "germinoma of the CNS", "Germinoma of the CNS", "intracranial germinoma", "Central nervous system germinoma", "central nervous system germinoma", "Central Nervous System Germinoma", "Germinoma of central nervous system", "germinoma of central nervous system", "Germinoma of Central Nervous System", "germinoma of the central nervous system", "Germinoma of the central nervous system", "Germinoma of the Central Nervous System", "central nervous system germinoma (disease)", "Germinoma of central nervous system (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system germinoma", "shortest_name_length": 9}
{"curie": "MONDO:0011783", "names": ["CDGIg", "CDG1G", "CDG-Ig", "CDG 1G", "CDG Ig", "ALG12-CDG", "ALG12-CDG (CDG-Ig)", "CDG syndrome type Ig", "mannosyltransferase 8 deficiency", "Mannosyltransferase 8 deficiency", "congenital disorder of glycosylation Ig", "congenital disorder of glycosylation 1g", "ALG12-congenital disorder of glycosylation", "Congenital Disorder of Glycosylation Type Ig", "congenital disorder of glycosylation type Ig", "Congenital disorder of glycosylation type 1g", "Congenital disorder of glycosylation type 1G", "Congenital disorder of glycosylation type Ig", "congenital disorder of glycosylation type 1g", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig", "Congenital Disorder of Glycosylation, Type IG", "congenital disorder of glycosylation, type Ig", "Carbohydrate deficient glycoprotein syndrome type Ig", "carbohydrate deficient glycoprotein syndrome type Ig", "ALG12-congenital disorder of glycosylation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ALG12-congenital disorder of glycosylation", "shortest_name_length": 5}
{"curie": "MONDO:0003398", "names": ["antegrade amnesia", "Antegrade amnesia", "Anterograde amnesia", "Anterograde Amnesia", "amnesia anterograde", "AMNESIA ANTEROGRADE", "anterograde amnesia", "Amnesia, Anterograde", "amnesia; anterograde", "Anterograde Amnesias", "Amnesias, Anterograde", "Anterograde Memory Loss", "Memory Loss, Anterograde", "Anterograde Memory Losses", "Memory Losses, Anterograde", "Anterograde memory impairment", "Anterograde amnesia (finding)", "anterograde amnesia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anterograde amnesia", "shortest_name_length": 17}
{"curie": "UMLS:C1334175", "names": ["Infectious Disorder by Site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infectious Disorder by Site", "shortest_name_length": 27}
{"curie": "MONDO:0011726", "names": ["Paod1", "PAOD1", "PERIPHERAL ARTERIAL OCCLUSIVE DISEASE 1", "peripheral arterial occlusive disease 1", "Peripheral Arterial Occlusive Disease 1", "peripheral arterial occlusive disease type 1", "Paod1 Peripheral Arterial Occlusive Disease 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peripheral arterial occlusive disease 1", "shortest_name_length": 5}
{"curie": "MONDO:0004874", "names": ["ganglion or cyst of synovium/tendon/bursa", "Other ganglion and cyst of synovium, tendon, and bursa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ganglion or cyst of synovium/tendon/bursa", "shortest_name_length": 41}
{"curie": "MONDO:0010776", "names": ["HYPERTENSION, HYPERCHOLESTEROLEMIA, AND HYPOMAGNESEMIA, MITOCHONDRIAL", "HYPOMAGNESEMIA, HYPERTENSION, AND HYPERCHOLESTEROLEMIA, MITOCHONDRIAL", "Hypomagnesemia, Hypertension, and Hypercholesterolemia, Mitochondrial", "hypomagnesemia, hypertension, and hypercholesterolemia, mitochondrial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypomagnesemia, hypertension, and hypercholesterolemia, mitochondrial", "shortest_name_length": 69}
{"curie": "UMLS:C0339916", "names": ["Viral upper respiratory tract infection", "Viral upper respiratory tract infections", "infection; respiratory tract, upper, viral", "respiratory tract; infection, upper, viral", "Upper respiratory tract infection viral NOS", "URTI - Viral upper respiratory tract infection", "Viral upper respiratory tract infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Viral upper respiratory tract infection", "shortest_name_length": 39}
{"curie": "MONDO:0019532", "names": ["wAHA", "wAIHA", "Warm AIHA", "warm AIHA", "warm antibody AIHA", "Warm type hemolytic anemia", "Warm type haemolytic anaemia", "Warm antibody hemolytic anemia", "warm antibody hemolytic anemia", "warm autoimmune hemolytic anemia", "Warm antibody haemolytic anaemia", "Warm autoimmune hemolytic anemia", "Warm autoimmune haemolytic anaemia", "warm antibody immune hemolytic anemia", "Hemolytic anemia due to warm antibody", "autoimmune hemolytic anemia, warm type", "Autoimmune hemolytic anemia, warm type", "Symptomatic warm type hemolytic anemia", "Warm type autoimmune hemolytic disease", "acquired warm antibody hemolytic anemia", "AIHA - Warm autoimmune hemolytic anemia", "Haemolytic anaemia due to warm antibody", "warm-reacting-antibody hemolytic anemia", "Warm Antibody Autoimmune Hemolytic Anemia", "warm antibody autoimmune hemolytic anemia", "AIHA - Warm autoimmune haemolytic anaemia", "Hemolytic anemia due to warm antibody, NOS", "Warm autoimmune hemolytic anemia (disorder)", "Haemolytic anaemia due to warm antibody, NOS", "Autoimmune hemolytic anemia, warm antibody type", "warm antibody immune hemolytic anemia (diagnosis)", "AUTOIMMUNE HEMOLYTIC ANEMIA INVOLVING WARM REACTING ANTIBODY", "Warm type (primary) (secondary) (symptomatic) autoimmune hemolytic anemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune hemolytic anemia, warm type", "shortest_name_length": 4}
{"curie": "MONDO:0008088", "names": ["neuropathy, with paraprotein in serum, cerebrospinal fluid and urine", "NEUROPATHY, WITH PARAPROTEIN IN SERUM, CEREBROSPINAL FLUID AND URINE", "Neuropathy, with Paraprotein in Serum, Cerebrospinal Fluid and Urine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuropathy, with paraprotein in serum, cerebrospinal fluid and urine", "shortest_name_length": 68}
{"curie": "UMLS:C0750989", "names": ["External Carotid Artery Thrombosis", "Thrombosis, External Carotid Artery"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "External Carotid Artery Thrombosis", "shortest_name_length": 34}
{"curie": "UMLS:C0855088", "names": ["Stage IV Nodular Sclerosis Hodgkin Lymphoma", "Hodgkin's disease nodular sclerosis stage IV", "Stage IV Nodular Sclerosis Hodgkin's Disease", "Nodular Sclerosis Hodgkin's Disease Stage IV", "Stage IV Nodular Sclerosis Hodgkin's Lymphoma", "Nodular Sclerosis Hodgkin's Lymphoma Stage IV", "Stage IV Nodular Sclerosis Classical Hodgkin Lymphoma", "Ann Arbor Stage IV Nodular Sclerosis Classic Hodgkin Lymphoma", "Ann Arbor Stage IV Nodular Sclerosis Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's disease nodular sclerosis stage IV", "shortest_name_length": 43}
{"curie": "UMLS:C2981272", "names": ["Stage IVC Differentiated Thyroid Gland Cancer", "Stage IVC Differentiated Thyroid Gland Carcinoma", "Stage IVC Differentiated Thyroid Gland Carcinoma AJCC v7", "Stage IVC Thyroid Gland Papillary or Follicular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Differentiated Thyroid Gland Carcinoma AJCC v7", "shortest_name_length": 45}
{"curie": "UMLS:C1333045", "names": ["CMML with Eosinophilia", "CMML with eosinophilia", "Chronic Myelomonocytic Leukemia with Eosinophilia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic Myelomonocytic Leukemia with Eosinophilia", "shortest_name_length": 22}
{"curie": "MONDO:0009539", "names": ["lall", "LALL", "LYMPHOMATOUS ALL", "Lymphomatous ALL", "lymphomatous All", "leukemia, acute lymphoblastic", "Lymphoblastic Leukemia, Acute, with Lymphomatous Features", "LYMPHOBLASTIC LEUKEMIA, ACUTE, WITH LYMPHOMATOUS FEATURES", "lymphoblastic leukemia, acute, with lymphomatous features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphoblastic leukemia, acute, with lymphomatous features", "shortest_name_length": 4}
{"curie": "MONDO:0008921", "names": ["CARNOSINEMIA", "carnosinemia", "Carnosinemia", "Carnosinaemia", "homocarnosinosis", "Carnosinase deficiency", "Carnosinase Deficiency", "CARNOSINASE DEFICIENCY", "carnosinase deficiency", "Carnosinemia (disorder)", "carnosinemia (diagnosis)", "Deficiency of carnosinase", "Homocarnosinase deficiency", "Serum carnosinase deficiency", "Deficiency of carnosinase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carnosinemia", "shortest_name_length": 12}
{"curie": "UMLS:C4744438", "names": ["Unresectable Non-Small Cell Lung Carcinoma", "Unresectable Lung Non-Small Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Lung Non-Small Cell Carcinoma", "shortest_name_length": 42}
{"curie": "UMLS:C3495827", "names": ["Lid sulcus deepened"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lid sulcus deepened", "shortest_name_length": 19}
{"curie": "UMLS:C5418754", "names": ["Benign Periampullary Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Periampullary Neoplasm", "shortest_name_length": 29}
{"curie": "UMLS:C1444680", "names": ["Posterior capsule fibrosis", "Posterior capsular thickening", "posterior capsule opacification", "Posterior Capsule Opacification", "Posterior capsule opacification", "posterior capsule opacification (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Posterior capsule opacification", "shortest_name_length": 26}
{"curie": "UMLS:C4724991", "names": ["Refractory Laryngeal Squamous Cell Carcinoma", "Refractory Laryngeal Throat Squamous Cell Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Laryngeal Squamous Cell Carcinoma", "shortest_name_length": 44}
{"curie": "MONDO:0016811", "names": ["renal tubulopathy-encephalopathy-liver failure syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal tubulopathy-encephalopathy-liver failure syndrome", "shortest_name_length": 55}
{"curie": "MONDO:0011475", "names": ["CMT4B2", "CMT 4B2", "Charcot-Marie-Tooth disease type 4B2", "Charcot-Marie-Tooth disease Type 4B2", "Charcot Marie Tooth disease type 4B2", "CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B2", "Charcot-Marie-Tooth disease, type 4B2", "Charcot-Marie-Tooth disease, Type 4B2", "SBF2 Charcot-Marie-Tooth disease type 4", "Charcot-Marie-Tooth neuropathy type 4B2", "Charcot-Marie-Tooth Neuropathy, Type 4B2", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4B2", "Charcot-Marie-Tooth neuropathy, type 4B2", "Charcot-Marie-Tooth disease type 4B2 (disorder)", "Charcot-Marie-Tooth disease Type 4B2 (diagnosis)", "Charcot-Marie-Tooth disease type 4 caused by mutation in SBF2", "Charcot-Marie-Tooth disease, Type 4B2, with early-onset glaucoma", "Charcot-Marie-Tooth disease, type 4B2, with early-onset glaucoma", "CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B2, WITH EARLY-ONSET GLAUCOMA", "Charcot-Marie-Tooth Neuropathy, Type 4B2, with Early-Onset Glaucoma", "Charcot-Marie-Tooth neuropathy, type 4B2, with early-onset glaucoma", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4B2, WITH EARLY-ONSET GLAUCOMA", "autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin sheaths type 4B2", "CHARCOT-MARIE-TOOTH DISEASE, WITH FOCALLY FOLDED MYELIN SHEATHS, AUTOSOMAL RECESSIVE, TYPE 4B2", "Charcot-Marie-Tooth Disease, With Focally Folded Myelin Sheaths, Autosomal Recessive, Type 4B2", "Charcot-Marie-Tooth disease, with focally folded myelin sheaths, autosomal recessive, type 4B2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 4B2", "shortest_name_length": 6}
{"curie": "UMLS:C0438414", "names": ["myoclonic encephalopathy", "Myoclonic Encephalopathy", "Myoclonic encephalopathy", "encephalopathy; myoclonic", "Encephalopathy, Myoclonic", "myoclonic; encephalopathy", "Myoclonic Encephalopathies", "Encephalopathies, Myoclonic", "Myoclonic encephalopathy (disorder)", "Myoclonic encephalopathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myoclonic Encephalopathy", "shortest_name_length": 24}
{"curie": "MONDO:0010431", "names": ["JBTS10", "JOUBERT SYNDROME 10", "Joubert syndrome 10", "Joubert Syndrome 10", "OFD1 Joubert syndrome", "Joubert syndrome type 10", "JOUBERT SYNDROME 10 (disorder)", "Joubert syndrome 10, X-linked recessive", "Joubert syndrome caused by mutation in OFD1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome 10", "shortest_name_length": 6}
{"curie": "UMLS:C1827266", "names": ["Decompensated chronic heart failure", "cardiac failure chronic decompensated", "decompensated chronic cardiac failure", "Decompensated chronic heart failure (disorder)", "decompensated chronic cardiac failure (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Decompensated chronic heart failure", "shortest_name_length": 35}
{"curie": "UMLS:C4763505", "names": ["Adrenal Gland Ganglioneuroma", "Adrenal Gland Ganglioneuroma (Schwannian Stroma-Dominant)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adrenal Gland Ganglioneuroma", "shortest_name_length": 28}
{"curie": "UMLS:C0005959", "names": ["Marrow Hyperplasia", "MARROW HYPERPLASIA", "Marrow hyperplasia", "marrow hyperplasia", "MARROW HYPERPLASIA OF", "Marrow hyperplasia of", "HYPERPLASIA BONE MARROW", "bone marrow hyperplasia", "bone hyperplasia marrow", "Bone marrow hyperplasia", "Bone Marrow Hyperplasia", "Hyperplasia bone marrow", "hyperplasia; bone marrow", "bone marrow; hyperplasia", "Hyperplasia of Bone Marrow", "Hematopoietic cell proliferation", "Haematopoietic cell proliferation", "Hematopoietic Cell Proliferations", "Bone marrow hyperplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone marrow hyperplasia", "shortest_name_length": 18}
{"curie": "UMLS:C1518724", "names": ["Ovarian Mucinous Carcinoid Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Mucinous Carcinoid Tumor", "shortest_name_length": 32}
{"curie": "MONDO:0014119", "names": ["MRT36", "NEDBGF", "MRT36, FORMERLY", "autosomal recessive mental retardation 36", "mental retardation, autosomal recessive 36", "intellectual disability-strabismus syndrome", "Intellectual Disability-Strabismus Syndrome", "Intellectual disability-strabismus syndrome", "intellectual disability, autosomal recessive 36", "mental retardation, autosomal recessive type 36", "intellectual disability with strabismus syndrome", "Intellectual disability with strabismus syndrome", "intellectual disability, autosomal recessive type 36", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36, FORMERLY", "Intellectual disability with strabismus syndrome (disorder)", "intellectual disability with strabismus syndrome (diagnosis)", "neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies", "NEURODEVELOPMENTAL DISORDER WITH BRAIN ABNORMALITIES, POOR GROWTH, AND DYSMORPHIC FACIES", "Neurodevelopmental Disorder with Brain Abnormalities, Poor Growth, and Dysmorphic Facies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability-strabismus syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0016945", "names": ["8p trisomy", "trisomy 8p", "Duplication 8p", "8p duplication", "partial trisomy 8p", "chromosome 8p duplication", "partial trisomy of chromosome 8p", "partial duplication of chromosome 8p", "partial trisomy of the short arm of chromosome 8", "partial duplication of the short arm of chromosome 8", "partial duplication of the short arm of chromosome type 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of the short arm of chromosome 8", "shortest_name_length": 10}
{"curie": "UMLS:C1332058", "names": ["AIDS-Related Pneumocystis Pneumonia", "AIDS-Related Pneumocystis carinii Pneumonia", "AIDS-Related Pneumocystis jirovecii Pneumonia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Pneumocystis Pneumonia", "shortest_name_length": 35}
{"curie": "MONDO:0025085", "names": ["animal viral hepatitis", "Animal Viral Hepatitis", "Viral Hepatitis, Animal", "hepatitis, viral, animal", "Hepatitis, Viral, Animal", "Animal Viral Hepatitides", "Viral Hepatitides, Animal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatitis, viral, animal", "shortest_name_length": 22}
{"curie": "UMLS:C1112363", "names": ["Underdose", "underdose", "Insufficient dosage", "Underdose (unintentional)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Underdose (unintentional)", "shortest_name_length": 9}
{"curie": "MONDO:0100091", "names": ["inherited PXE", "inherited pseudoxanthoma elasticum", "inherited Gronblad Strandberg syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited pseudoxanthoma elasticum", "shortest_name_length": 13}
{"curie": "UMLS:C5447503", "names": ["Refractory Esophageal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Esophageal Adenocarcinoma", "shortest_name_length": 36}
{"curie": "MONDO:0003902", "names": ["Brainstem Angioblastoma", "brainstem angioblastoma", "Brain Stem Angioblastoma", "brain stem angioblastoma", "brainstem hemangioblastoma", "angioblastoma of brainstem", "Angioblastoma of Brainstem", "Brain Stem Hemangioblastoma", "brain stem hemangioblastoma", "Angioblastoma of Brain Stem", "angioblastoma of brain stem", "Hemangioblastoma of Brainstem", "hemangioblastoma of brainstem", "angioblastoma of the brainstem", "hemangioblastoma of brain stem", "Angioblastoma of the Brainstem", "Hemangioblastoma of Brain Stem", "Angioblastoma of the Brain Stem", "angioblastoma of the brain stem", "Hemangioblastoma of the Brainstem", "hemangioblastoma of the brainstem", "Hemangioblastoma of the Brain Stem", "hemangioblastoma of the brain stem", "Brain Stem Capillary Hemangioblastoma", "brain stem capillary hemangioblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brain stem hemangioblastoma", "shortest_name_length": 23}
{"curie": "UMLS:C0877294", "names": ["Metastasis to Placenta", "Metastases to placenta", "Metastasis to the Placenta", "Metastatic Tumor to the Placenta", "Metastatic Neoplasm to the Placenta", "placental neoplasm malignant secondary", "Secondary malignant neoplasm of placenta", "Metastatic malignant neoplasm of placenta", "Metastatic malignant neoplasm to placenta", "Metastatic Malignant Neoplasm to the Placenta", "Metastatic Malignant Neoplasm in the Placenta", "Metastatic malignant neoplasm to placenta (disorder)", "Secondary malignant neoplasm of placenta (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Neoplasm to the Placenta", "shortest_name_length": 22}
{"curie": "MONDO:0054804", "names": ["MCPH21", "microcephaly 21, primary, autosomal recessive", "microcephaly 21, PRIMARY, autosomal recessive", "MICROCEPHALY 21, PRIMARY, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly 21, primary, autosomal recessive", "shortest_name_length": 6}
{"curie": "MONDO:0004262", "names": ["breast myoepitheliosis", "Breast Myoepitheliosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast myoepitheliosis", "shortest_name_length": 22}
{"curie": "MONDO:0100197", "names": ["HPIV infectious disorder", "parainfluenza (disorder)", "parainfluenza infectious disease", "parainfluenza infectious disorder", "human parainfluenza virus infectious disorder", "human parainfluenza viruses infectious disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parainfluenza infectious disease", "shortest_name_length": 24}
{"curie": "MONDO:0008528", "names": ["tear protein, anodal", "TEAR PROTEIN, ANODAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tear protein, anodal", "shortest_name_length": 20}
{"curie": "MONDO:0010213", "names": ["XPe", "XPE", "XP5", "XP-E", "XP group E", "XP, GROUP E", "XP, Group E", "XERODERMA PIGMENTOSUM V", "xeroderma pigmentosum V", "Xeroderma Pigmentosum V", "xeroderma pigmentosum 5", "xeroderma pigmentosum group E", "xeroderma pigmentosum, type 5", "Xeroderma pigmentosum group E", "Xeroderma Pigmentosum Group E", "Xeroderma pigmentosum, group E", "xeroderma pigmentosum group type E", "Xeroderma pigmentosum, group E (disorder)", "xeroderma pigmentosum, complementation group E", "Xeroderma Pigmentosum, Complementation Group E", "XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E", "xeroderma pigmentosum, complementation group type E", "xeroderma pigmentosum, group E, DDB-negative subtype"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "xeroderma pigmentosum group E", "shortest_name_length": 3}
{"curie": "UMLS:C3489704", "names": ["Vision Disability", "Disability, Vision", "Vision Disabilities", "Disabilities, Vision"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vision Disability", "shortest_name_length": 17}
{"curie": "UMLS:C0266769", "names": ["Placenta Multiplex", "Multilobate placenta", "Multilobate Placenta", "Placenta Multipartita", "Placenta, multilobate", "multipartita placenta", "Placenta multipartita", "multipartita; placenta", "placenta; multipartita", "Placenta multipartita (disorder)", "Placenta multipartita (diagnosis)", "placenta malformation multipartita", "Multilobate Chorionic Surface Shape"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Placenta multipartita", "shortest_name_length": 18}
{"curie": "MONDO:0024625", "names": ["lacrimal gland disease", "LACRIMAL GLAND DISORDER", "Lacrimal gland disorder", "lacrimal gland; disorder", "disease of lacrimal gland", "Disorder of lacrimal gland", "disorder of lacrimal gland", "disorders of lacrimal gland", "Lacrimal gland disorder NOS", "Disorder of lacrimal gland, NOS", "lacrimal gland disease or disorder", "disease or disorder of lacrimal gland", "Disorder of lacrimal gland (disorder)", "disease (or disorder); lacrimal gland", "disorders of lacrimal gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of lacrimal gland", "shortest_name_length": 22}
{"curie": "MONDO:0100185", "names": ["IRS", "IRD", "IRIS", "immune restoration disease", "Immune Restoration Disease", "Immune Restoration Diseases", "Immune Restoration Syndrome", "Restoration Syndrome, Immune", "Immune Reconstitution Disease", "Reconstitution Disease, Immune", "Immune Reconstitution Syndrome", "immune reconstitution syndrome", "Reconstitution Syndrome, Immune", "Immune Reconstitution Syndromes", "Immune Reconstitution Inflammatory Syndrome", "immune reconstitution inflammatory syndrome", "Immune reconstitution inflammatory syndrome", "immune reconstitution inflammatory syndrome associated with Kaposi sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immune reconstitution inflammatory syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0700132", "names": ["melanoma, non-human animal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melanoma, non-human animal", "shortest_name_length": 26}
{"curie": "MONDO:0019464", "names": ["HCD", "BALLARD DISEASE", "SELIGMANN DISEASE", "HEAVY CHAIN DISEASE", "heavy chain disease", "Heavy chain disease", "Heavy Chain Disease", "Heavy Chain Diseases", "Heavy chain disease, NOS", "Heavy chain disease (disorder)", "heavy chain disease (diagnosis)", "Heavy chain disease (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heavy chain disease", "shortest_name_length": 3}
{"curie": "MONDO:0009873", "names": ["Kopysc Barczyk Krol syndrome", "Kopysc-Barczyk-Krol syndrome", "Euhidrotic ectodermal dysplasia", "TRICHODENTAL DYSPLASIA WITH HYPEROPIA", "Trichodental dysplasia with hyperopia", "Pilodental dysplasia with refractive errors", "PILODENTAL DYSPLASIA WITH REFRACTIVE ERRORS", "PILODENTAL dysplasia with refractive errors", "Pilodental dysplasia-refractive errors syndrome", "pilodental dysplasia-refractive errors syndrome", "Pilodental dysplasia, refractive errors syndrome", "Pilodental dysplasia, refractive errors syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pilodental dysplasia-refractive errors syndrome", "shortest_name_length": 28}
{"curie": "UMLS:C3899119", "names": ["Fetal SGA with Oligohydramnios", "Fetal SGA with Oligohydraminois", "Fetus Small for Gestational Age with Oligohydraminos", "Fetal Small for Gestational Age with Oligohydraminos", "Fetal Small for Gestational Age with Oligohydramnios"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fetus Small for Gestational Age with Oligohydraminos", "shortest_name_length": 30}
{"curie": "MONDO:0004277", "names": ["GC", "gc", "PAS", "PAC", "Clap", "CLAP", "clap", "claps", "The clap", "gonorrhea", "GONORRHEA", "Gonorrhea", "GONOCOCCAL", "gonococcal", "Gonococcal", "Gonorrhoea", "gonorrhoea", "Gonorrhea NOS", "Gonorrhea, NOS", "Gonorrhoea NOS", "gonococcal infection", "Gonococcal infection", "Gonorrhea (disorder)", "Gonococcal Infection", "GONOCOCCAL INFECTION", "gonococcal; infection", "gonococcal infections", "infection; gonococcal", "Gonococcal infections", "Crosti-gianotti syndrome", "Gianotti Crosti syndrome", "GC - Gonococcus infection", "Gonococcal infection, NOS", "GCI - Gonococcal infection", "Neisseria gonorrheae infection", "Neisseria gonorrhoeae Infection", "Neisseria gonorrhoeae infection", "Gonococcal infection, unspecified", "infections, Neisseria gonorrhoeae", "acrodermatitis, papular infantile", "gonococcal infections (diagnosis)", "papular acrodermatitis of childhood", "acrodermatitis, infantile lichenoid", "gonorrhea; specified site not listed", "Infection due to Neisseria gonorrhoeae", "chronic gonococcal infectious disease of upper genitourinary tract", "chronic gonococcal infectious disease of lower genitourinary tract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gonorrhea", "shortest_name_length": 2}
{"curie": "MONDO:0002433", "names": ["cranial nerve cancer", "cancer of cranial nerve", "Malignant Cranial Nerve Tumor", "malignant cranial nerve tumor", "Malignant Cranial Nerve Tumors", "Cranial Nerve Tumors, Malignant", "malignant tumor of cranial nerve", "cranial nerve malignant neoplasm", "Malignant tumor of cranial nerve", "malignant cranial nerve neoplasm", "Malignant cranial nerve neoplasm", "Tumors, Cranial Nerve, Malignant", "Malignant Tumor of Cranial Nerve", "Malignant Cranial Nerve Neoplasm", "Malignant tumour of cranial nerve", "cranial nerve neoplasm, malignant", "Cranial Nerve Neoplasm, Malignant", "Malignant Cranial Nerve Neoplasms", "Cranial Nerve Neoplasms, Malignant", "malignant neoplasm of cranial nerve", "Malignant Neoplasm of Cranial Nerve", "Neoplasms, Cranial Nerve, Malignant", "malignant neoplasm of cranial nerves", "malignant tumor of the cranial nerve", "Malignant neoplasm of cranial nerves", "malignant tumor of the Cranial nerve", "Malignant Tumor of the Cranial Nerve", "Malignant cranial nerve neoplasm NOS", "Malignant Neoplasm of the Cranial Nerve", "Malignant neoplasm of cranial nerve NOS", "malignant neoplasm of the cranial nerve", "Malignant neoplasm of cranial nerve, NOS", "Malignant tumor of cranial nerve (disorder)", "malignant neoplasm of cranial nerve (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant cranial nerve neoplasm", "shortest_name_length": 20}
{"curie": "UMLS:C1707444", "names": ["CCC", "Columnar Cell Change", "Breast Blunt Duct Adenosis", "Breast Columnar Cell Change", "Blunt Duct Adenosis of Breast", "Columnar Cell Change of Breast", "Blunt Duct Adenosis of the Breast", "Columnar Cell Change of the Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Columnar Cell Change of the Breast", "shortest_name_length": 3}
{"curie": "UMLS:C1336321", "names": ["Stage II Subdiaphragmatic Nodular Lymphocyte Predominant Hodgkin Lymphoma", "Stage II Subdiaphragmatic Nodular Lymphocyte Predominant Hodgkin's Lymphoma", "Subdiaphragm Stage II Hodgkin's Lymphoma Nodular Lymphocyte Predominance Type", "Stage II Subdiaphragmatic Hodgkin Lymphoma Nodular Lymphocyte Predominant Type", "Stage II Subdiaphragmatic Hodgkin's Lymphoma Nodular Lymphocyte Predominant Type", "Stage II Subdiaphragmatic Hodgkin's Disease Nodular Lymphocyte Predominance Type", "Ann Arbor Stage II Subdiaphragmatic Nodular Lymphocyte Predominant Hodgkin Lymphoma", "Stage II Hodgkin's Disease Nodular Lymphocyte Predominance Type below the Diaphragm", "Stage II Hodgkin's Lymphoma Nodular Lymphocyte Predominance Type Below the Diaphragm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage II Subdiaphragmatic Nodular Lymphocyte Predominant Hodgkin Lymphoma", "shortest_name_length": 73}
{"curie": "UMLS:C0278738", "names": ["Stage IV Lymphoblastic Lymphoma", "NHL, lymphoblastic stage IV childhood", "NHL, lymphoblastic metastatic childhood", "Stage IV Pediatric Lymphoblastic Lymphoma", "Childhood Lymphoblastic Lymphoma Stage IV", "stage IV childhood lymphoblastic lymphoma", "Pediatric Lymphoblastic Lymphoma Stage IV", "Pediatric Stage IV Lymphoblastic Lymphoma", "Childhood Stage IV Lymphoblastic Lymphoma", "Stage IV Childhood Lymphoblastic Lymphoma", "stage IV lymphoblastic childhood lymphoma", "metastatic lymphoblastic childhood lymphoma", "metastatic childhood lymphoblastic lymphoma", "Metastatic Pediatric Lymphoblastic Lymphoma", "Ann Arbor Stage IV Childhood Lymphoblastic Lymphoma", "Stage IV Childhood Precursor Lymphoblastic Lymphoma", "childhood non-Hodgkin's lymphoma, lymphoblastic stage IV", "lymphoblastic stage IV non-Hodgkin's lymphoma, childhood", "Non-Hodgkin's lymphoma, lymphoblastic stage IV childhood", "pediatric lymphoblastic non-Hodgkin's lymphoma, stage IV", "lymphoma, non-Hodgkin's, lymphoblastic stage IV childhood", "metastatic lymphoblastic childhood non-Hodgkin's lymphoma", "Non-Hodgkin's lymphoma, lymphoblastic metastatic childhood", "pediatric lymphoblastic non-Hodgkin's lymphoma, metastatic", "lymphoblastic metastatic non-Hodgkin's lymphoma, childhood", "childhood non-Hodgkin's lymphoma, lymphoblastic metastatic", "lymphoma, non-Hodgkin's, lymphoblastic metastatic childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Childhood Lymphoblastic Lymphoma", "shortest_name_length": 31}
{"curie": "MONDO:0007910", "names": ["LIPOPROTEIN TYPES--Lt SYSTEM", "lipoprotein types--Lt system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lipoprotein types--Lt system", "shortest_name_length": 28}
{"curie": "MONDO:0010155", "names": ["CDS", "DCS", "DCs", "NLSDI", "Dorfman-Chanarin disease", "Chanarin-Dorfman disease", "CHANARIN-DORFMAN DISEASE", "Chanarin-Dorfman syndrome", "CHANARIN-DORFMAN SYNDROME", "Chanarin-Dorfman Syndrome", "DORFMAN-CHANARIN SYNDROME", "Dorfman-Chanarin syndrome", "Dorfman-Chanarin Syndrome", "Chanarin-Miranda syndrome", "Dorfman Chanarin syndrome", "Neutral lipid storage disease", "Neutral lipid storage myopathy", "ICHTHYOTIC NEUTRAL LIPID STORAGE DISEASE", "ichthyotic neutral Lipid storage disease", "Ichthyotic neutral lipid storage disease", "Lipidosis with triglyceride storage disease", "Triglyceride Storage Disease with Ichthyosis", "Triglyceride storage disease with ichthyosis", "Neutral lipid storage disease with ichthyosis", "neutral lipid storage disease with ichthyosis", "NEUTRAL LIPID STORAGE DISEASE WITH ICHTHYOSIS", "Neutral Lipid Storage Disease With Ichthyosis", "neutral Lipid storage disease with ichthyosis", "neutral lipid storage disease with ichthyotic", "Lipid storage myopathy AND congenital ichthyosis", "Lipid storage myopathy and congenital ichthyosis", "ichthyosiform erythroderma with leukocyte vacuolation", "Ichthyosiform erythroderma with leucocyte vacuolation", "Ichthyosiform erythroderma with leukocyte vacuolation", "ICHTHYOSIFORM ERYTHRODERMA WITH LEUKOCYTE VACUOLATION", "Triglyceride storage disease with ichthyosis (disorder)", "disorder of cornification 12 (neutral lipid storage type)", "triglyceride storage disease with impaired long-chain fatty acid oxidation", "Triglyceride storage disease with impaired long-chain fatty acid oxidation", "TRIGLYCERIDE STORAGE DISEASE WITH IMPAIRED LONG-CHAIN FATTY ACID OXIDATION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dorfman-Chanarin disease", "shortest_name_length": 3}
{"curie": "MONDO:0013318", "names": ["Early repolarization syndrome", "EARLY REPOLARIZATION SYNDROME", "Early repolarisation syndrome", "early repolarization syndrome", "EARLY REPOLARIZATION ASSOCIATED WITH VENTRICULAR FIBRILLATION", "early repolarization associated with ventricular fibrillation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early repolarization associated with ventricular fibrillation", "shortest_name_length": 29}
{"curie": "MONDO:0017688", "names": ["disorder of glycolysis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of glycolysis", "shortest_name_length": 22}
{"curie": "MONDO:0005764", "names": ["Follicular dendritic cell tumor", "Follicular dendritic cell tumour", "follicular dendritic cell tumour", "Follicular Dendritic Cell Sarcoma", "follicular Dendritic cell sarcoma", "follicular dendritic cell sarcoma", "Follicular Dendritic cell sarcoma", "Follicular dendritic cell sarcoma", "Dendritic Cell Sarcoma, Follicular", "sarcoma of follicular dendritic cell", "Follicular Dendritic Cell Sarcoma/Tumor", "follicular Dendritic cell sarcoma/tumor", "follicular dendritic cell sarcoma (diagnosis)", "Follicular dendritic cell sarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "follicular dendritic cell sarcoma", "shortest_name_length": 31}
{"curie": "MONDO:0032787", "names": ["HPE12", "holoprosencephaly 12 with or without pancreatic agenesis", "HOLOPROSENCEPHALY 12 WITH OR WITHOUT PANCREATIC AGENESIS", "holoprosencephaly 12, with or without pancreatic agenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "holoprosencephaly 12 with or without pancreatic agenesis", "shortest_name_length": 5}
{"curie": "MONDO:0007793", "names": ["HCH", "HYPOCHONDROPLASIA", "Hypochondroplasia", "hypochondroplasia", "Hypochondrodysplasia", "Hypochondroplasia syndrome", "Hypochondroplasia (disorder)", "short; stature, hypochondroplastic", "stature; short, hypochondroplastic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypochondroplasia", "shortest_name_length": 3}
{"curie": "UMLS:C1302749", "names": ["Hamartomatosis", "Congenital hamartoma", "congenital hamartoma", "Congenital Hamartoma", "Hamartomatous disease", "Congenital hamartosis", "Congenital hamartoma (disorder)", "congenital hamartoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital hamartoma", "shortest_name_length": 14}
{"curie": "MONDO:0045030", "names": ["diarrhea; noninfective", "non-infective diarrhea", "noninfective; diarrhea", "Non-infective diarrhea", "Non-infective diarrhoea", "Noninfectious diarrhea, NOS", "Noninfectious diarrhoea, NOS", "presumed non-infectious diarrhea", "non-infectious diarrheal disease", "Presumed non-infectious diarrhea", "Non-infective diarrhea (disorder)", "Presumed non-infectious diarrhoea", "Non-infective diarrhea (diagnosis)", "intestinal disorder diarrhea non-infective"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-infectious diarrheal disease", "shortest_name_length": 22}
{"curie": "MONDO:0800179", "names": ["periprosthetic joint infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "periprosthetic joint infection", "shortest_name_length": 30}
{"curie": "UMLS:C0751710", "names": ["Single Peroxisomal Dysfunction", "Single Peroxisomal Dysfunctions", "Peroxisomal Dysfunction, Single", "Dysfunction, Single Peroxisomal", "Dysfunctions, Single Peroxisomal", "Peroxisomal Dysfunctions, Single", "Loss of single peroxisomal function", "Loss of single peroxisomal function (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peroxisomal Dysfunction, Single", "shortest_name_length": 30}
{"curie": "MONDO:0011799", "names": ["DFNB33", "autosomal recessive deafness 33", "Deafness, Autosomal Recessive 33", "DEAFNESS, AUTOSOMAL RECESSIVE 33", "deafness, autosomal recessive 33", "autosomal recessive nonsyndromic deafness 33", "autosomal recessive nonsyndromic hearing loss 33", "autosomal recessive nonsyndromic deafness type 33"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 33", "shortest_name_length": 6}
{"curie": "UMLS:C5237035", "names": ["Recurrent Ovarian High-Grade Serous Adenocarcinoma", "Recurrent Ovarian High Grade Serous Adenocarcinoma", "Recurrent High Grade Ovarian Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Ovarian High Grade Serous Adenocarcinoma", "shortest_name_length": 50}
{"curie": "MONDO:0012112", "names": ["CMH10", "hypertrophic cardiomyopathy 10", "cardiomyopathy, hypertrophic, 10", "MYL2 hypertrophic cardiomyopathy", "hypertrophic cardiomyopathy type 10", "Cardiomyopathy, Familial Hypertrophic, 10", "CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10", "cardiomyopathy, familial hypertrophic, 10", "cardiomyopathy, familial hypertrophic, type 10", "hypertrophic cardiomyopathy caused by mutation in MYL2", "Cardiomyopathy, Hypertrophic, Mid-Left Ventricular Chamber Type, 2", "cardiomyopathy, hypertrophic, mid-left ventricular chamber type, 2", "CARDIOMYOPATHY, HYPERTROPHIC, MID-LEFT VENTRICULAR CHAMBER TYPE, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophic cardiomyopathy 10", "shortest_name_length": 5}
{"curie": "MONDO:0004495", "names": ["Myotonic cataract", "myotonic cataract", "Myotonic Cataract", "Myotonic cataract (disorder)", "myotonic; cataract (etiology)", "myotonic cataract (diagnosis)", "cataract; myotonic (etiology)", "myotonic; cataract (manifestation)", "cataract; myotonic (manifestation)", "cataract; myotonic disorders (etiology)", "cataract; myotonic disorders (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myotonic cataract", "shortest_name_length": 17}
{"curie": "UMLS:C0685206", "names": ["Domed head", "Dome-Shaped Head", "Domed head (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Domed head", "shortest_name_length": 10}
{"curie": "MONDO:0003052", "names": ["granulomatous endometritis", "Granulomatous Endometritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "granulomatous endometritis", "shortest_name_length": 26}
{"curie": "MONDO:0008622", "names": ["BORK SYNDROME", "Bork syndrome", "Bork Stender Schmidt syndrome", "Tricho-retino-dento-digital syndrome", "tricho-retino-dento-digital syndrome", "uncombable hair, retinal pigmentary dystrophy, dental anomalies, and brachydactyly", "Uncombable hair, retinal pigmentary dystrophy, dental anomalies, and brachydactyly", "UNCOMBABLE HAIR, RETINAL PIGMENTARY DYSTROPHY, DENTAL ANOMALIES, AND BRACHYDACTYLY", "uncombable hair-retinal pigmentary dystrophy-dental anomalies-brachydactyly syndrome", "Uncombable hair-retinal pigmentary dystrophy-dental anomalies-brachydactyly syndrome", "Uncombable hair, retinal pigmentary dystrophy, dental anomaly and brachydactyly syndrome", "Uncombable hair, retinal pigmentary dystrophy, dental anomaly and brachydactyly syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tricho-retino-dento-digital syndrome", "shortest_name_length": 13}
{"curie": "UMLS:C1112793", "names": ["Vascular implant infection", "Vascular Implant Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vascular implant infection", "shortest_name_length": 26}
{"curie": "UMLS:C1516430", "names": ["Cervical Rhabdomyoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Rhabdomyoma", "shortest_name_length": 20}
{"curie": "MONDO:0020631", "names": ["DEE92", "IECEE2", "developmental and epileptic encephalopathy 92", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 92", "epileptic encephalopathy, infantile or early childhood, 2", "EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epileptic encephalopathy, infantile or early childhood, 2", "shortest_name_length": 5}
{"curie": "UMLS:C0856554", "names": ["Hepatic cancer metastatic", "metastatic hepatic cancer", "metastatic liver carcinoma", "Metastatic liver carcinoma", "Metastatic Liver Carcinoma", "carcinoma liver metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatic cancer metastatic", "shortest_name_length": 25}
{"curie": "UMLS:C5444610", "names": ["Superficial ALT/WDLPS", "Superficial Atypical Lipomatous Tumor", "Superficial Well Differentiated Liposarcoma", "Superficial Well-Differentiated Liposarcoma", "Superficial well differentiated liposarcoma", "Well differentiated liposarcoma of superficial soft tissue", "Superficial Atypical Lipomatous Tumor/Well-Differentiated Liposarcoma", "Superficial Atypical Lipomatous Tumor/Well Differentiated Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Superficial Atypical Lipomatous Tumor/Well Differentiated Liposarcoma", "shortest_name_length": 21}
{"curie": "MONDO:0008752", "names": ["AxD", "ALXDRD", "ALEXANDER DISEASE", "alexander disease", "Alexander Disease", "Alexander disease", "Alexander syndrome", "Alexanders Disease", "alexanders disease", "alexander's disease", "Alexander's disease", "Alexander's Disease", "Fibrinoid leukodystrophy", "fibrinoid leukodystrophy", "alexanders leukodystrophy", "Demyelinogenic Leukodystrophy", "demyelinogenic leukodystrophy", "Alexander's disease (disorder)", "dysmyelinogenic leukodystrophy", "Dysmyelinogenic Leukodystrophy", "fibrinoid leukodystrophy (diagnosis)", "Fibrinoid Degeneration of Astrocytes", "Leukodystrophy with Rosenthal Fibers", "fibrinoid degeneration of astrocytes", "megalencephaly with hyaline panneuropathy", "Progressive astrocyte degeneration syndrome", "megalencephaly in infancy accompanied by progressive spasticity and dementia", "macrocephaly with feeblemindedness and encephalopathy with peculiar deposits"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alexander disease", "shortest_name_length": 3}
{"curie": "UMLS:C3272980", "names": ["Non-Neoplastic Gallbladder Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Gallbladder Disorder", "shortest_name_length": 35}
{"curie": "UMLS:C4521824", "names": ["IVB", "Stage IVB Hilar Cholangiocarcinoma", "Stage IVB Hilar Cholangiocarcinoma AJCC v8", "Stage IVB Perihilar Cholangiocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Hilar Cholangiocarcinoma AJCC v8", "shortest_name_length": 3}
{"curie": "MONDO:0008476", "names": ["SMD", "SmD", "Semdc", "SEMDC", "SEMDSTWK", "SMED type 1", "SMED, TYPE I", "Smed, Type I", "Smed, type 1", "Sed Strudwick", "Strudwick syndrome", "STRUDWICK SYNDROME", "SMED Strudwick type", "Smed, Strudwick Type", "Semd, Strudwick Type", "SEMD, STRUDWICK TYPE", "Smed, Strudwick type", "SEMD, Strudwick type", "SMED, STRUDWICK TYPE", "DAPPLED METAPHYSIS SYNDROME", "Dappled metaphysis syndrome", "dappled metaphysis syndrome", "SPONDYLOMETAPHYSEAL DYSPLASIA", "Spondylometaphyseal Dysplasia", "Spondylometaphyseal dysplasia", "spondylometaphyseal dysplasia", "Spondylometaphyseal Dysplasia (Smd)", "Spondylometaphyseal dysplasia (disorder)", "spondyloepimetaphyseal dysplasia Strudwick type", "SPONDYLOEPIMETAPHYSEAL DYSPLASIA, STRUDWICK TYPE", "spondyloepimetaphyseal dysplasia, Strudwick type", "Spondyloepimetaphyseal dysplasia, Strudwick type", "SEMD - spondyloepimetaphyseal dysplasia, Strudwick type", "spondylometaepiphyseal dysplasia congenita, Strudwick type", "spondyloepimetaphyseal dysplasia congenita, Strudwick type", "SPONDYLOMETAEPIPHYSEAL DYSPLASIA CONGENITA, STRUDWICK TYPE", "Spondylometaepiphyseal Dysplasia Congenita, Strudwick Type", "Spondyloepimetaphyseal dysplasia, Strudwick type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepimetaphyseal dysplasia, Strudwick type", "shortest_name_length": 3}
{"curie": "UMLS:C0861149", "names": ["Proarrhythmic effect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Proarrhythmic effect", "shortest_name_length": 20}
{"curie": "UMLS:C0860207", "names": ["DILI", "Drug-induced liver injury", "Drug-Induced Liver Injury", "Drug Induced Liver Injury", "Drug-induced liver disease", "Liver Injury, Drug-Induced", "Drug-Induced Liver Disease", "disease drug induced liver", "Injury, Drug-Induced Liver", "Drug Induced Liver Disease", "drug-induced liver disease", "Liver Injury, Drug Induced", "Drug-induced hepatotoxicity", "Liver Disease, Drug-Induced", "Drug-Induced Liver Diseases", "diseases drug induced liver", "Disease, Drug-Induced Liver", "Drug induced hepatotoxicity", "Drug-Induced Liver Injuries", "Liver Diseases, Drug-Induced", "Diseases, Drug-Induced Liver", "Injuries, Drug-Induced Liver", "Liver Injuries, Drug-Induced", "diseases drugs inducing liver", "drug-induced diorder of liver", "Drug-induced disorder of liver", "drug-induced diorder of liver (diagnosis)", "Drug-induced disorder of liver (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drug-Induced Liver Disease", "shortest_name_length": 4}
{"curie": "MONDO:0017576", "names": ["ferm", "Ferms", "46,XX DSD", "46, XX DSD", "Gynandrism", "Genetic 46,XX DSD", "female pseudohermaphroditism", "Female pseudohermaphroditism", "Pseudohermaphroditism female", "Female Pseudohermaphroditism", "pseudohermaphroditism; female", "Female Pseudohermaphroditisms", "Pseudohermaphroditism, Female", "PSEUDOHERMAPHRODITISM, FEMALE", "Pseudohermaphroditisms, Female", "Female pseudohermaphroditism NOS", "46,XX disorder of sex development", "46,XX disorders of Sex development", "46,XX Disorders of Sex Development", "46, XX Disorders of Sex Development", "46,XX Differences of Sex Development", "46,XX differences of Sex development", "Pseudohermaphroditism syndrome, female", "Female pseudohermaphroditism (disorder)", "female pseudohermaphroditism (diagnosis)", "Genetic 46,XX disorder of sex development", "46,XX disorder of sex development (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XX disorder of sex development", "shortest_name_length": 4}
{"curie": "UMLS:C4521651", "names": ["IIA", "Stage IIA Esophageal Adenocarcinoma", "Pathologic Stage IIA Esophageal Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IIA Esophageal Adenocarcinoma AJCC v8", "shortest_name_length": 3}
{"curie": "MONDO:0011678", "names": ["chromosome 11p15-p14 deletion syndrome", "Homozygous 11p15-p14 Deletion Syndrome", "HOMOZYGOUS 11p15-p14 DELETION SYNDROME", "homozygous 11P15-p14 deletion syndrome", "HYPERINSULINISM, INFANTILE, WITH ENTEROPATHY AND DEAFNESS", "hyperinsulinism, infantile, with enteropathy and deafness", "Hyperinsulinism, Infantile, with Enteropathy and Deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "homozygous 11P15-p14 deletion syndrome", "shortest_name_length": 38}
{"curie": "UMLS:C1333862", "names": ["Grade II Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade II Neuroendocrine Carcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C5237272", "names": ["Locally Advanced Paranasal Sinus Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Paranasal Sinus Carcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0044750", "names": ["Lassa virus infection", "lassa virus infectious disease", "infection caused by Lassa virus", "Infection caused by Lassa virus", "Infection caused by Lassa virus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lassa virus infectious disease", "shortest_name_length": 21}
{"curie": "UMLS:C4744474", "names": ["Epididymal Papillary Cystadenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epididymal Papillary Cystadenoma", "shortest_name_length": 32}
{"curie": "UMLS:C1335901", "names": ["Salivary Gland Intraductal Papilloma", "intraductal papilloma of salivary gland", "intraductal papilloma of salivary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intraductal papilloma of salivary gland", "shortest_name_length": 36}
{"curie": "UMLS:C1561230", "names": ["necrosis soft tissue", "Soft tissue necrosis", "necrosis soft tissue (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Soft tissue necrosis", "shortest_name_length": 20}
{"curie": "UMLS:C2981418", "names": ["Stage IIIB Small Intestinal Gastrointestinal Stromal Tumor", "Stage IIIB Small Intestinal Gastrointestinal Stromal Tumor (GIST)", "Stage IIIB Small Intestinal Gastrointestinal Stromal Tumor AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Small Intestinal Gastrointestinal Stromal Tumor", "shortest_name_length": 58}
{"curie": "MONDO:0002103", "names": ["Münchhausen", "factitious illness", "Factitious illness", "factitious disorder", "Factitious Disorder", "munchausen syndrome", "MUNCHAUSEN SYNDROME", "Munchausen syndrome", "disorder factitious", "Münchausen syndrome", "Factitious disorder", "Munchausen Syndrome", "Factitious disorders", "Syndrome, Munchausen", "disorder; factitious", "Factitious Disorders", "munchhausen syndrome", "factitious; disorder", "factitious disorders", "FACTITIOUS DISORDERS", "Munchhausen Syndrome", "Munchhausen syndrome", "munchausens syndrome", "Disorders, Factitious", "munchhausens syndrome", "Munchausen's syndrome", "Munchhausens syndrome", "Peregrinating patient", "Münchausen's syndrome", "munchausen's syndrome", "Syndrome, Munchhausen", "munchhausen's syndrome", "Factitious disorder NOS", "disturbance; factitious", "Hospital hopper syndrome", "Factitious disorder, NOS", "hospital hopper syndrome", "Hospital addiction syndrome", "hospital addiction syndrome", "Hospital-Addiction Syndrome", "Hospital Addiction Syndrome", "Hospital-Addiction Syndromes", "Syndrome, Hospital-Addiction", "Syndrome, Hospital Addiction", "Syndromes, Hospital-Addiction", "intentional; produced disorder", "disorder; intentional produced", "Factitious disorder (disorder)", "factitious disorder (diagnosis)", "disease (or disorder); feigning", "Munchausen syndrome (diagnosis)", "Munchausen's syndrome (disorder)", "intentional production; symptoms", "symptoms; intentional production", "factitious illness (psychological)", "feigned; disease, without obvious motivation", "feigned; disorder, without obvious motivation", "disorder; feigned, without obvious motivation", "disease (or disorder); artificial, factitious", "Factitious illness with psychological symptoms", "factitious disorder with psychological symptoms", "Factitious disorder with psychological symptoms", "disease (or disorder); feigned, without obvious motivation", "factitious disorder with psychological symptoms (diagnosis)", "Factitious disorder with predominantly psychological signs and symptoms", "Factitious disorder with predominantly psychological signs and symptoms (disorder)", "Intentional production or feigning of symptoms or disabilities, either physical or psychological [factitious disorder]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "factitious disorder", "shortest_name_length": 11}
{"curie": "MONDO:0015588", "names": ["limbic encephalitis", "Limbic Encephalitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "limbic encephalitis", "shortest_name_length": 19}
{"curie": "UMLS:C0042386", "names": ["Hemorrhagic Vasculitis", "Hemorrhagic vasculitis", "Haemorrhagic vasculitis", "Vasculitis, Hemorrhagic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vasculitis, Hemorrhagic", "shortest_name_length": 22}
{"curie": "UMLS:C5419079", "names": ["Advanced Myxofibrosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Myxofibrosarcoma", "shortest_name_length": 25}
{"curie": "MONDO:0003347", "names": ["Inflammatory Leiomyosarcoma", "inflammatory leiomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory leiomyosarcoma", "shortest_name_length": 27}
{"curie": "MONDO:0003410", "names": ["Wolffian duct adenocarcinoma", "mesonephric duct adenocarcinoma", "Cervical Mesonephric Adenocarcinoma", "cervical mesonephric adenocarcinoma", "HPV- Independent Cervical Adenocarcinoma, Mesonephric Type", "HPV- Independent Cervical Adenocarcinoma, Mesonephric-Type", "Human Papillomavirus-Independent Cervical Adenocarcinoma, Mesonephric Type", "Human Papillomavirus-Independent Cervical Adenocarcinoma, Mesonephric-Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wolffian duct adenocarcinoma", "shortest_name_length": 28}
{"curie": "UMLS:C4551541", "names": ["Vaginal Cancer Stage III", "Stage III Vaginal Cancer", "stage III vaginal cancer", "AJCC Stage III Vaginal Cancer", "FIGO Stage III Vagina Carcinoma", "Stage III Vaginal Cancer AJCC v6", "FIGO Stage III Vaginal Carcinoma", "Stage III Vaginal Cancer AJCC v7", "FIGO Stage III Carcinoma of Vagina", "Stage III Vaginal Carcinoma AJCC v6", "Stage III Vaginal Carcinoma AJCC v7", "FIGO Stage III Carcinoma of the Vagina", "Stage III Vaginal Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Vaginal Cancer AJCC v6 and v7", "shortest_name_length": 24}
{"curie": "UMLS:C1520072", "names": ["AMNGT", "Atypical Vulvar Nevus", "Atypical Melanocytic Nevus, Genital Type", "Atypical Melanocytic Nevus of Genital Type", "Atypical Melanocytic Nevus of the Genital Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypical Melanocytic Nevus of Genital Type", "shortest_name_length": 5}
{"curie": "UMLS:C0750921", "names": ["Lichtheim Sign", "Lichtheims Sign", "Lichtheim's Sign", "Sign, Lichtheim's", "Dejerine-Lichtheim Phenomenon", "Dejerine Lichtheim Phenomenon", "Phenomenon, Dejerine-Lichtheim"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dejerine-Lichtheim Phenomenon", "shortest_name_length": 14}
{"curie": "UMLS:C0855174", "names": ["Relapsed Bladder Adenocarcinoma", "Recurrent Bladder Adenocarcinoma", "Bladder adenocarcinoma recurrent", "Bladder Adenocarcinoma, Recurrent", "Relapsed Adenocarcinoma of Bladder", "Recurrent Adenocarcinoma of Bladder", "Relapsed Adenocarcinoma of the Bladder", "Recurrent Adenocarcinoma of the Bladder", "Relapsed Urinary Bladder Adenocarcinoma", "Recurrent Urinary Bladder Adenocarcinoma", "Relapsed Adenocarcinoma of Urinary Bladder", "Recurrent Adenocarcinoma of Urinary Bladder", "Relapsed Adenocarcinoma of the Urinary Bladder", "Recurrent Adenocarcinoma of the Urinary Bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder adenocarcinoma recurrent", "shortest_name_length": 31}
{"curie": "UMLS:C1400574", "names": ["Dialysis Catheter Infection", "dialysis catheter; infection", "infection; dialysis catheter", "infection; catheter, dialysis catheter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dialysis Catheter Infection", "shortest_name_length": 27}
{"curie": "UMLS:C0278746", "names": ["Relapsed Vagina Cancer", "recurrent vagina cancer", "Relapsed Vaginal Cancer", "Recurrent Vagina Cancer", "Recurrent Vaginal Cancer", "recurrent vaginal cancer", "Vaginal cancer recurrent", "vagina cancer, recurrent", "vaginal cancer, recurrent", "Relapsed Cancer of Vagina", "Cancer of vagina recurrent", "Recurrent Cancer of Vagina", "Recurrent Vaginal Carcinoma", "Relapsed Cancer of the Vagina", "Recurrent Cancer of the Vagina", "recurrent cancer of the vagina", "cancer of the vagina, recurrent", "recurrent carcinoma of the vagina", "carcinoma of the vagina, recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal cancer recurrent", "shortest_name_length": 22}
{"curie": "UMLS:C4524073", "names": ["Low Anterior Resection Syndrome", "Low anterior resection syndrome", "LARS - low anterior resection syndrome", "Low anterior resection syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Anterior Resection Syndrome", "shortest_name_length": 31}
{"curie": "MONDO:0005469", "names": ["hypotension postural", "POSTURAL HYPOTENSION", "postural hypotension", "Postural hypotension", "HYPOTENSION POSTURAL", "Hypotension postural", "Postural Hypotension", "Hypotension;postural", "hypotension; postural", "Hypotension, Postural", "Hypotension, postural", "postural; hypotension", "Orthostatic hypotension", "hypotension orthostatic", "ORTHOSTATIC HYPOTENSION", "Hypotension orthostatic", "Orthostatic Hypotension", "Hypotension;orthostatic", "orthostatic hypotension", "HYPOTENSION ORTHOSTATIC", "Hypotension, orthostatic", "Hypotension, Orthostatic", "hypotension; orthostatic", "orthostatic; hypotension", "HYPOTENSION, ORTHOSTATIC", "orthostatic hypotension (disease)", "Orthostatic hypotension (disorder)", "orthostatic hypotension (diagnosis)", "orthostatic hypotension was observed", "orthostatic hypotension (physical finding)", "Decrease in blood pressure upon standing up"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orthostatic hypotension", "shortest_name_length": 20}
{"curie": "UMLS:C5235853", "names": ["Advanced Thyroid Gland Medullary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Thyroid Gland Medullary Carcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0004706", "names": ["Discoid lupus eyelid", "Discoid lupus erythematosus eyelid", "discoid lupus erythematosus of eyelid", "Discoid lupus erythematosus of eyelid", "Discoid lupus erythematosus of eyelid (disorder)", "discoid lupus erythematosus of eyelid (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "discoid lupus erythematosus of eyelid", "shortest_name_length": 20}
{"curie": "UMLS:C1336823", "names": ["Follicular Myxoma", "Trichogenic Myxoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Follicular Myxoma", "shortest_name_length": 17}
{"curie": "UMLS:C0684686", "names": ["soft tissue metastasis", "metastasis soft tissue", "soft tissue metastases", "Metastases to soft tissue", "Metastasis to soft tissue", "Metastases to soft tissue NOS", "neoplasm - soft tissue malignant secondary", "secondary malignant neoplasm of soft tissue", "secondary malignant neoplasm of soft tissues", "Secondary malignant neoplasm of soft tissues", "Metastatic malignant neoplasm to soft tissues", "Metastatic malignant neoplasm of soft tissues", "Metastatic Malignant Neoplasm to Soft Tissues", "Metastatic Malignant Neoplasm to the Soft Tissues", "Metastatic Malignant Neoplasm in the Soft Tissues", "secondary malignant neoplasm of soft tissue (diagnosis)", "Metastatic malignant neoplasm to soft tissues (disorder)", "Secondary malignant neoplasm of connective and other soft tissues", "Metastatic malignant neoplasm to connective and other soft tissues", "Secondary malignant neoplasm of connective and other soft tissues, NOS", "Metastatic malignant neoplasm to connective and other soft tissues, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to soft tissues", "shortest_name_length": 22}
{"curie": "UMLS:C0334391", "names": ["Complex epithelial tumor", "Complex Epithelial Tumor", "Complex epithelial tumour", "Complex Epithelial Neoplasm", "Complex Tumor of Epithelium", "Complex epithelial neoplasm", "COMPLEX EPITHELIAL NEOPLASMS", "Complex Epithelial Neoplasms", "Complex Neoplasm of Epithelium", "Complex Tumor of the Epithelium", "Complex Neoplasm of the Epithelium", "Mixed squamous cell and glandular papilloma", "Complex epithelial neoplasm (morphologic abnormality)", "Mixed squamous cell and glandular papilloma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Complex epithelial neoplasm", "shortest_name_length": 24}
{"curie": "UMLS:C3272529", "names": ["Intestinal NET", "Intestinal Neuroendocrine Tumor", "Intestinal Well Differentiated Endocrine Tumor", "Intestinal Well Differentiated Endocrine Tumor/Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal Neuroendocrine Tumor", "shortest_name_length": 14}
{"curie": "MONDO:0010558", "names": ["Del(X)(q21)", "Monosomy Xq21", "Ayazi syndrome", "Xq21 microdeletion syndrome", "Choroideremia deafness obesity", "choroideremia deafness obesity", "CHROMOSOME Xq21 DELETION SYNDROME", "chromosome Xq21 deletion syndrome", "choroideremia-deafness-obesity syndrome", "Choroideremia with Deafness and Obesity", "Xq21 deletion syndrome, X-linked recessive", "choroideremia, deafness, and mental retardation", "Choroideremia, obesity, and congenital deafness", "choroideremia, obesity, and congenital deafness", "CHOROIDEREMIA, DEAFNESS, AND MENTAL RETARDATION", "Choroideremia with deafness and obesity syndrome", "Choroideraemia with deafness and obesity syndrome", "choroideremia, deafness, and intellectual disability", "Choroideremia with deafness and obesity syndrome (disorder)", "Choroideremia with deafness and obesity syndrome (diagnosis)", "hereditary choroidal dystrophy choroideremia with deafness and obesity syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choroideremia-deafness-obesity syndrome", "shortest_name_length": 11}
{"curie": "UMLS:C4764208", "names": ["Refractory Endometrial Clear Cell Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Endometrial Clear Cell Adenocarcinoma", "shortest_name_length": 48}
{"curie": "UMLS:C2981692", "names": ["Stage 0 Eyelid Carcinoma", "Stage 0 Eyelid Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Eyelid Carcinoma AJCC v7", "shortest_name_length": 24}
{"curie": "MONDO:0013295", "names": ["ATOD9", "atopic dermatitis 9", "dermatitis, ATOPIC, 9", "dermatitis, atopic, 9", "DERMATITIS, ATOPIC, 9", "atopic dermatitis type 9", "dermatitis, atopic, susceptibility to, 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermatitis, atopic, 9", "shortest_name_length": 5}
{"curie": "MONDO:0003790", "names": ["prostatic urethra urothelial carcinoma", "Prostatic Urethra Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostatic urethra urothelial carcinoma", "shortest_name_length": 38}
{"curie": "UMLS:C4054405", "names": ["Nephropathy due to Analgesic Drugs"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephropathy due to Analgesic Drugs", "shortest_name_length": 34}
{"curie": "MONDO:0000355", "names": ["UCMD", "UCMD1", "LGMDR22", "Ullrich", "Ullrich disease", "ULLRICH DISEASE", "scleroatonic Ullrich disease", "Scleroatonic Ullrich Disease", "scleroatonic muscular dystrophy", "Scleroatonic muscular dystrophy", "Muscular Dystrophy, Scleroatonic", "MUSCULAR DYSTROPHY, SCLEROATONIC", "Ullrich congenital muscular dystrophy", "Ullrich Congenital Muscular Dystrophy", "ULLRICH CONGENITAL MUSCULAR DYSTROPHY", "ULLRICH CONGENITAL MUSCULAR DYSTROPHY 1", "ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY", "Ullrich scleroatonic muscular dystrophy", "Ullrich congenital muscular dystrophy 1", "Late onset scleroatonic familial myopathy", "Congenital muscular dystrophy, Ullrich type", "congenital muscular dystrophy, Ullrich type", "Ullrich congenital muscular dystrophy (disorder)", "Ullrich congenital muscular dystrophy (diagnosis)", "Congenita hypotonic - sclerotic muscular dystrophy", "late onset scleroatonic familial myopathy (subtype)", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 22"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ullrich congenital muscular dystrophy", "shortest_name_length": 4}
{"curie": "MONDO:0016668", "names": ["S-Beta Thalassemia", "S-Beta thalassemia", "Hb S beta-thalassemia", "Hb S-Beta Thalassemia", "Hb S-Beta thalassemia", "HbS - beta-thalassemia", "sickle beta-thalassemia", "sickle beta thalassemia", "Sickle Beta Thalassemia", "Thalassemia Hb-S disease", "Sickle Cell-Beta-Thalassemia", "Sickle Cell-Beta Thalassemia", "sickle cell-Beta-thalassemia", "Sickle cell-beta-thalassemia", "sickle cell-Beta thalassemia", "Sickle cell-beta-thalassaemia", "Hemoglobin S/beta thalassemia", "Hemoglobin S beta thalassemia", "HbS-beta-thalassemia syndrome", "Hemoglobin S/Beta Thalassemia", "Haemoglobin S/beta thalassaemia", "Hemoglobin sickle-beta thalassemia", "sickle beta-thalassemia (diagnosis)", "Thalassemia with hemoglobin S disease", "sickle cell - beta-thalassemia disease", "Sickle cell-beta-thalassemia (disorder)", "Thalassaemia with haemoglobin S disease", "anemia hemolytic sickle beta-thalassemia", "sickle cell-beta-thalassemia disease syndrome", "Double heterozygous for Hb S and beta thalassemia", "Double heterozygous for Hb S and beta thalassaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sickle cell-beta-thalassemia disease syndrome", "shortest_name_length": 18}
{"curie": "MONDO:0004235", "names": ["Diverticulitis", "DIVERTICULITIS", "diverticulitis", "Diverticulitides", "Diverticulitis NOS", "Diverticulitis, NOS", "Diverticulitis (disorder)", "diverticulitis (diagnosis)", "Diverticulitis (diagnosis)", "Diverticulitis (morphologic abnormality)", "digestive tract diverticulum inflammation", "inflammation of digestive tract diverticulum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diverticulitis", "shortest_name_length": 14}
{"curie": "UMLS:C0940747", "names": ["Pancreatic Duct Stenosis", "Pancreatic duct stenosis", "pancreatic duct stenosis", "pancreatic duct stenosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Duct Stenosis", "shortest_name_length": 24}
{"curie": "MONDO:0017237", "names": ["hereditary sensorimotor neuropathy with hyperelastic skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary sensorimotor neuropathy with hyperelastic skin", "shortest_name_length": 57}
{"curie": "MONDO:0013565", "names": ["FANCG", "fanconi anemia complementation group g", "Fanconi anemia complementation group G", "FANCONI ANEMIA, COMPLEMENTATION GROUP G", "Fanconi Anemia, Complementation Group G", "Fanconi anemia, complementation group G", "Fanconi anemia complementation group type G", "Fanconi Anemia, complementation group type G", "Fanconi anemia complementation group G (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fanconi anemia complementation group G", "shortest_name_length": 5}
{"curie": "MONDO:0006006", "names": ["Warty carcinoma", "warty carcinoma", "Verrucous Carcinoma", "carcinoma verrucous", "Verrucous carcinoma", "verrucous carcinoma", "Verrucous Carcinomas", "Carcinoma, Verrucous", "verrucous carcinomas", "Carcinomas, Verrucous", "Verrucous carcinoma NOS", "Condylomatous carcinoma", "Verrucous carcinoma, NOS", "verrucous squamous carcinoma", "Verrucous Squamous Carcinoma", "verrucous epidermoid carcinoma", "Verrucous epidermoid carcinoma", "Verrucous Epidermoid Carcinoma", "verrucous carcinoma (diagnosis)", "Verrucous squamous cell carcinoma", "Verrucous Squamous Cell Carcinoma", "verrucous squamous cell carcinoma", "squamous cell carcinoma verrucous", "verrucous epidermoid cell carcinoma", "Verrucous Epidermoid Cell Carcinoma", "Verrucous SCC (squamous cell carcinoma)", "SCC - Verrucous squamous cell carcinoma", "Verrucous squamous cell carcinoma (disorder)", "Verrucous carcinoma (morphologic abnormality)", "squamous cell carcinoma verrucous (diagnosis)", "verrucous carcinoma NOS (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "verrucous carcinoma", "shortest_name_length": 15}
{"curie": "UMLS:C1697438", "names": ["Viral cystitis", "viral cystitis", "Cystitis viral", "Cystitis caused by virus", "viral cystitis (diagnosis)", "Cystitis caused by virus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Viral cystitis", "shortest_name_length": 14}
{"curie": "UMLS:C0023869", "names": ["Lithiasis", "lithiasis", "Lithiases", "Calculoses", "calculosis", "Calculosis", "Lithiasis, NOS", "Calculosis, NOS", "Lithiasis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lithiasis", "shortest_name_length": 9}
{"curie": "MONDO:0013764", "names": ["JBTS16", "JOUBERT SYNDROME 16", "Joubert syndrome 16", "TMEM138 Joubert syndrome", "Joubert syndrome type 16", "Joubert syndrome caused by mutation in TMEM138"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome 16", "shortest_name_length": 6}
{"curie": "MONDO:0033115", "names": ["SCAR25", "autosomal recessive spinocerebellar ataxia 25", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 25", "spinocerebellar ataxia, autosomal recessive 25"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia, autosomal recessive 25", "shortest_name_length": 6}
{"curie": "UMLS:C0521540", "names": ["Brain stem bleeding", "Brainstem hemorrhage", "Brainstem Hemorrhage", "brainstem hemorrhage", "HEMORRHAGE BRAIN STEM", "Brainstem haemorrhage", "Brain stem hemorrhage", "Hemorrhage brain stem", "brain stem hemorrhage", "brain stem; hemorrhage", "brain stem haemorrhage", "Brain stem haemorrhage", "hemorrhage; brain stem", "Haemorrhage brain stem", "HAEMORRHAGE BRAIN STEM", "Brain stem hemorrhage (disorder)", "brain stem hemorrhage (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brain stem hemorrhage", "shortest_name_length": 19}
{"curie": "MONDO:0022643", "names": ["carcinoma of the vocal tract", "laryngeal vocal fold carcinoma", "carcinoma of laryngeal vocal fold"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma of the vocal tract", "shortest_name_length": 28}
{"curie": "UMLS:C4287896", "names": ["Borderline Ovarian Clear Cell Tumor/Atypical Proliferative Ovarian Clear Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Ovarian Clear Cell Tumor/Atypical Proliferative Ovarian Clear Cell Tumor", "shortest_name_length": 83}
{"curie": "MONDO:0009217", "names": ["SYNDROME FANCONI-LIKE", "Fanconi-Like Syndrome", "Fanconi-like syndrome", "Syndrome Fanconi-like", "FANCONI-LIKE SYNDROME", "Fanconi like syndrome", "Fanconi-like syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fanconi-like syndrome", "shortest_name_length": 21}
{"curie": "MONDO:0019416", "names": ["X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome", "shortest_name_length": 102}
{"curie": "MONDO:0100240", "names": ["inherited thrombophilia", "hereditary thrombophilia", "thrombophilia, hereditary", "hereditary hypercoagulable disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited thrombophilia", "shortest_name_length": 23}
{"curie": "UMLS:C0751053", "names": ["Postictal Confusion", "Postictal confusion", "Confusion Postictal", "Post-Ictal Confusion", "Postseizure confusion", "Confusion, Post Ictal", "Confusion, Post-Ictal", "Postepileptic confusion", "Postseizure confusion (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Confusion, Post-Ictal", "shortest_name_length": 19}
{"curie": "UMLS:C1336101", "names": ["Stage 0a Renal Pelvis and Ureter Cancer", "Stage 0a Renal Pelvis and Ureter Cancer AJCC v7", "Stage 0a Renal Pelvis and Ureter Urothelial Carcinoma", "Stage 0a Renal Pelvis and Ureter Urothelial Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0a Renal Pelvis and Ureter Cancer AJCC v7", "shortest_name_length": 39}
{"curie": "MONDO:0014797", "names": ["LMPH3", "LMPHM6", "LMPH3, FORMERLY", "PIEZO1-related LRHF/GLD", "LYMPHATIC MALFORMATION 6", "lymphatic malformation 6", "lymphedema, hereditary, 3", "lymphedema, hereditary, III", "lymphedema, hereditary, type III", "LYMPHEDEMA, HEREDITARY, III, FORMERLY", "Generalized lymphatic dysplasia of Fotiou", "GENERALIZED LYMPHATIC DYSPLASIA OF FOTIOU", "generalized lymphatic dysplasia of Fotiou", "Generalised lymphatic dysplasia of Fotiou", "PIEZO1-related lymphatic-related hydrops fetalis", "PIEZO1-related generalized lymphatic dysplasia with systemic involvement", "PIEZO1-related generalised lymphatic dysplasia with systemic involvement", "PIEZO1-related generalised lymphatic dysplasia with non-immune hydrops fetalis", "PIEZO1-related generalized lymphatic dysplasia with non-immune hydrops fetalis", "Piezo type mechanosensitive ion channel component 1-related generalized lymphatic dysplasia with non-immune hydrops fetalis", "Piezo type mechanosensitive ion channel component 1-related generalised lymphatic dysplasia with non-immune hydrops fetalis", "Piezo type mechanosensitive ion channel component 1-related generalized lymphatic dysplasia with non-immune hydrops fetalis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphatic malformation 6", "shortest_name_length": 5}
{"curie": "UMLS:C0475598", "names": ["Melena Neonatal", "neonatal melena", "Neonatal Melena", "Neonatal melena", "Melena neonatal", "newborn; melena", "melena; newborn", "Melaena neonatal", "Neonatal melaena", "Melena Neonatorum", "Neonatal melena (disorder)", "neonatal melena (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neonatal melena", "shortest_name_length": 15}
{"curie": "UMLS:C4521908", "names": ["Stage III Rectosigmoid Cancer", "Stage III Rectosigmoid Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Rectosigmoid Cancer AJCC v7", "shortest_name_length": 29}
{"curie": "MONDO:0011114", "names": ["EAC", "MFT1", "epithelioma adenoides cysticum", "Brooke-Fordyce Trichoepitheliomas", "BROOKE-FORDYCE TRICHOEPITHELIOMAS", "multiple familial trichoepithelioma", "Familial multiple trichoepithelioma", "trichoepithelioma multiple familial", "familial multiple trichoepithelioma", "Trichoepithelioma multiple familial", "Multiple Familial Trichoepithelioma", "Familial multiple trichoepitheliomata", "Trichoepithelioma, Multiple Familial, 1", "TRICHOEPITHELIOMA, MULTIPLE FAMILIAL, 1", "Epithelioma adenoides cysticum of Brooke", "EPITHELIOMA ADENOIDES CYSTICUM OF BROOKE", "epithelioma Adenoides Cysticum of Brooke", "Hereditary Multiple Benign Cystic Epithelioma", "hereditary multiple benign cystic epithelioma", "epithelioma, hereditary multiple benign cystic", "EPITHELIOMA, HEREDITARY MULTIPLE BENIGN CYSTIC", "Epithelioma, hereditary multiple benign cystic", "Familial multiple trichoepitheliomata (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial multiple trichoepithelioma", "shortest_name_length": 3}
{"curie": "MONDO:0021104", "names": ["Alcoholic fatty liver", "FATTY LIVER ALCOHOLIC", "alcoholic fatty liver", "Fatty liver alcoholic", "Alcoholic Fatty Liver", "Fatty liver, alcoholic", "Fatty Liver, Alcoholic", "Alcoholic Steatohepatitis", "Alcoholic steatohepatitis", "alcoholic Steatohepatitis", "alcohol induced fatty liver", "Alcoholic-induced fatty liver", "Alcoholic Fatty Liver Disease", "alcoholic fatty liver disease", "Alcoholic fatty liver disease", "Alcoholic fatty liver (disorder)", "alcoholic fatty liver (diagnosis)", "Steatohepatitis caused by ethanol", "alcohol; liver degeneration, fatty", "alcohol; fatty degeneration of liver", "Steatohepatitis caused by ethanol (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alcoholic fatty liver disease", "shortest_name_length": 21}
{"curie": "MONDO:0010318", "names": ["FGS4", "FG SYNDROME 4", "FG syndrome 4", "CASK FG syndrome", "cask FG syndrome", "FG syndrome type 4", "FG syndrome caused by mutation in CASK", "FG syndrome caused by mutation in cask", "Mental Retardation, X-Linked, Cask-Related", "Mental Retardation, X-Linked, With Nystagmus", "mental retardation, with or without nystagmus", "MENTAL RETARDATION, X-LINKED, WITH OR WITHOUT NYSTAGMUS", "mental retardation, X-linked, with or without Nystagmus", "X-linked intellectual disability with or without nystagmus", "intellectual disability, X-linked, with or without Nystagmus", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, WITH OR WITHOUT NYSTAGMUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FG syndrome 4", "shortest_name_length": 4}
{"curie": "UMLS:C1333447", "names": ["Esophageal Glandular Dysplasia", "Esophageal Glandular Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Glandular Intraepithelial Neoplasia", "shortest_name_length": 30}
{"curie": "MONDO:0000895", "names": ["nonmucinous bronchioloalveolar adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nonmucinous bronchioloalveolar adenocarcinoma", "shortest_name_length": 45}
{"curie": "UMLS:C1518374", "names": ["nonmalignant hematologic disorder", "Non-Malignant Hematologic and Lymphocytic Disorder", "Non-Neoplastic Hematologic and Lymphocytic Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Hematologic and Lymphocytic Disorder", "shortest_name_length": 33}
{"curie": "UMLS:C1709048", "names": ["Mitral perforation", "Mitral Perforation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mitral perforation", "shortest_name_length": 18}
{"curie": "UMLS:C0036219", "names": ["Jensen Sarcoma", "Sarcoma, Jensen"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sarcoma, Jensen", "shortest_name_length": 14}
{"curie": "MONDO:0004930", "names": ["corticosteroid; glaucoma", "glaucoma; corticosteroid", "Steroid-induced glaucoma", "Glaucoma steroid-induced", "steroid-induced glaucoma", "Corticosteroid-induced glaucoma", "corticosteroid-induced glaucoma", "Corticosteroid-induced glaucoma, NOS", "Corticosteroid-induced glaucoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "steroid-induced glaucoma", "shortest_name_length": 24}
{"curie": "MONDO:0015817", "names": ["aggressive primary cutaneous T-cell lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aggressive primary cutaneous T-cell lymphoma", "shortest_name_length": 44}
{"curie": "MONDO:0060629", "names": ["NDHMSR", "neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant", "neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive", "NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive", "shortest_name_length": 6}
{"curie": "MONDO:0021960", "names": ["Ureteritis", "ureteritis", "Ureteritis, NOS", "ureter inflammation", "Ureteritis (disorder)", "ureteritis (diagnosis)", "Inflammation of ureter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ureteritis", "shortest_name_length": 10}
{"curie": "UMLS:C0278787", "names": ["Relapsed CML", "Relapsed CGL", "relapsed CML", "relapsed CGL", "CGL, relapsed", "CML, relapsed", "relapsing CML", "CML, relapsing", "relapsed chronic myelocytic leukemia", "relapsed chronic myelogenous leukemia", "chronic myelocytic leukemia, relapsed", "Relapsed Chronic Myelogenous Leukemia", "myelocytic leukemia, relapsed chronic", "Recurrent Chronic Myelogenous Leukemia", "leukemia, relapsed chronic myelogenous", "myelogenous leukemia, relapsed chronic", "relapsed chronic granulocytic leukemia", "recurrent chronic myelogenous leukemia", "chronic myelogenous leukemia, relapsed", "chronic granulocytic leukemia, relapsed", "chronic myelogenous leukemia, relapsing", "granulocytic leukemia, relapsed chronic", "chronic myelogenous leukemia in relapse", "Recurrent Chronic Myelogenous Leukemia (CML)", "CML (chronic myelogenous leukemia) in relapse", "chronic myelogenous leukemia in relapse (diagnosis)", "Recurrent Chronic Myelogenous Leukemia, BCR-ABL1 Positive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Chronic Myelogenous Leukemia, BCR-ABL1 Positive", "shortest_name_length": 12}
{"curie": "UMLS:C0233528", "names": ["Asocial behavior", "Asocial behaviour", "Asocial behavior (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Asocial behavior", "shortest_name_length": 16}
{"curie": "UMLS:C0684324", "names": ["PGK deficiency", "phosphoglycerate kinase deficiency", "Deficiency of phosphoglycerate kinase", "phosphoglycerate kinase (PGK) deficiency", "red cell phosphoglycerate kinase deficiency", "erythrocyte phosphoglycerate kinase deficiency", "Deficiency of phosphoglycerate kinase (disorder)", "phosphoglycerate kinase deficiency hereditary non-spherocytic anemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Deficiency of phosphoglycerate kinase", "shortest_name_length": 14}
{"curie": "MONDO:0003126", "names": ["breast angioma", "Breast Angioma", "angioma of breast", "hemangioma breast", "Breast Hemangioma", "breast hemangioma", "Angioma of Breast", "breast hemangiomas", "Hemangioma of breast", "Hemangioma of Breast", "hemangioma of breast", "Haemangioma of breast", "Angioma of the breast", "angioma of the breast", "haemangioma of breast", "Angioma of the Breast", "hemangioma of the breast", "Hemangioma of the Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast hemangioma", "shortest_name_length": 14}
{"curie": "MONDO:0006103", "names": ["pheochromocytoma, benign", "PHEOCHROMOCYTOMA, BENIGN", "Localized Pheochromocytoma", "benign adrenal gland pheochromocytoma", "Benign Adrenal Gland Pheochromocytoma", "adrenal gland pheochromocytoma, benign", "Benign pheochromocytoma of adrenal gland", "benign pheochromocytoma of adrenal gland", "Non-Metastatic Adrenal Gland Pheochromocytoma", "benign pheochromocytoma of adrenal gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign adrenal gland pheochromocytoma", "shortest_name_length": 24}
{"curie": "UMLS:C3829185", "names": ["Stage III", "Masaoka Stage III", "Masaoka-Koga Stage III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Masaoka-Koga Stage III", "shortest_name_length": 9}
{"curie": "MONDO:0017826", "names": ["null pituitary adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "null pituitary adenoma", "shortest_name_length": 22}
{"curie": "UMLS:C2205024", "names": ["Appendix NEC", "Appendix NEC G3", "Appendix Neuroendocrine Carcinoma", "Neuroendocrine carcinoma of appendix", "neuroendocrine carcinoma of appendix", "Appendix High Grade Neuroendocrine Carcinoma", "Neuroendocrine carcinoma of appendix (disorder)", "neuroendocrine carcinoma of appendix (diagnosis)", "Appendix Poorly Differentiated Endocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neuroendocrine carcinoma of appendix", "shortest_name_length": 12}
{"curie": "UMLS:C1336237", "names": ["Ovarian Cancer Stage IIIC", "Stage IIIC Ovarian Cancer", "FIGO Stage IIIC Ovarian Cancer", "AJCC Stage IIIC Ovarian Cancer", "FIGO Stage IIIC Cancer of Ovary", "FIGO Stage IIIC Ovarian Carcinoma", "Stage IIIC Ovarian Cancer AJCC v6", "Stage IIIC Ovarian Cancer AJCC v7", "FIGO Stage IIIC Carcinoma of Ovary", "FIGO Stage IIIC Cancer of the Ovary", "Stage IIIC Ovarian Epithelial Cancer", "FIGO Stage IIIC Carcinoma of the Ovary", "Stage IIIC Ovarian Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Ovarian Cancer", "shortest_name_length": 25}
{"curie": "UMLS:C0861754", "names": ["Rectal adenocarcinoma recurrent", "Recurrent Rectal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rectal adenocarcinoma recurrent", "shortest_name_length": 31}
{"curie": "MONDO:0006915", "names": ["Polyradiculoneuropathy", "polyradiculoneuropathy", "Polyradiculoneuropathies", "polyradiculoneuropathies", "Polyradiculoneuropathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyradiculoneuropathy", "shortest_name_length": 22}
{"curie": "MONDO:0007586", "names": ["EXT2", "Ext2", "EXT2 Gene", "EXT2 exostoses, multiple", "multiple exostosis type II", "exostoses (Multiple) 2 Gene", "exostoses, multiple, type 2", "EXOSTOSES, MULTIPLE, TYPE II", "exostoses, multiple, type II", "Exostoses, Multiple, Type II", "Exostosin Glycosyltransferase 2 Gene", "multiple exostosis type II (diagnosis)", "exostoses, multiple caused by mutation in EXT2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exostoses, multiple, type 2", "shortest_name_length": 4}
{"curie": "UMLS:C4526841", "names": ["Osteosarcoma by AJCC v7 Stage", "Primary Bone Osteosarcoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Osteosarcoma by AJCC v7 Stage", "shortest_name_length": 29}
{"curie": "MONDO:0021074", "names": ["premalignant", "precancerous state", "Precancerous State", "Premalignant State", "premalignant state", "premalignant condition", "Precancerous Condition", "Precancerous condition", "precancerous condition", "nonmalignant condition", "Premalignant Condition", "Condition, Precancerous", "Precancerous Conditions", "precancerous conditions", "Precancerous conditions", "Conditions, Precancerous"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "precancerous condition", "shortest_name_length": 12}
{"curie": "MONDO:0000977", "names": ["Chondroid Lipoma", "Chondroid lipoma", "chondroid lipoma", "Chondroid lipoma (disorder)", "Chondroid lipoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chondroid lipoma", "shortest_name_length": 16}
{"curie": "MONDO:0011336", "names": ["FHL4", "Hlh4", "HLH4", "Hplh4", "HPLH4", "familial hemophagocytic lymphohistiocytosis 4", "Hemophagocytic lymphohistiocytosis, familial, 4", "HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 4", "hemophagocytic lymphohistiocytosis, familial, 4", "STX11 genetic hemophagocytic lymphohistiocytosis", "familial hemophagocytic lymphohistiocytosis type 4", "hemophagocytic lymphohistiocytosis, familial, type 4", "genetic hemophagocytic lymphohistiocytosis caused by mutation in STX11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial hemophagocytic lymphohistiocytosis 4", "shortest_name_length": 4}
{"curie": "MONDO:0030903", "names": ["HPS11", "Hermansky-Pudlak syndrome", "HERMANSKY-PUDLAK SYNDROME 11", "Hermansky-Pudlak syndrome 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hermansky-Pudlak syndrome 11", "shortest_name_length": 5}
{"curie": "MONDO:0008846", "names": ["TFQTL1", "Atransferrinemia", "atransferrinemia", "ATRANSFERRINEMIA", "Congenital atransferinemia", "Congenital Atransferrinemia", "hereditary atransferrinemia", "Hereditary Atransferrinemia", "Congenital atransferrinemia", "congenital atransferrinemia", "atransferrinemia; congenital", "Familial Hypotransferrinemia", "familial hypotransferrinemia", "Familial hypotransferrinemia", "Congenital atransferrinaemia", "hypotransferrinemia, familial", "HYPOTRANSFERRINEMIA, FAMILIAL", "Hypotransferrinemia, Familial", "Atransferrinemia (hereditary)", "Atransferrinaemia (hereditary)", "congenital hypotransferrinemia", "Congenital hypotransferrinemia", "Congenital atransferrinemia (disorder)", "transferrin serum level quantitative trait locus 1", "TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atransferrinemia", "shortest_name_length": 6}
{"curie": "MONDO:0013185", "names": ["LPRS5", "TLR1 leprosy", "leprosy, protection against", "susceptibility to leprosy 5", "LEPROSY, PROTECTION AGAINST", "leprosy, susceptibility to, 5", "LEPROSY, SUSCEPTIBILITY TO, 5", "leprosy, susceptibility to, type 5", "leprosy caused by mutation in TLR1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leprosy, susceptibility to, 5", "shortest_name_length": 5}
{"curie": "MONDO:0021205", "names": ["Ear disease", "Ear Disease", "ear disease", "disease ear", "Disease;ear", "Ear disorder", "DISORDER EAR", "Ear Diseases", "ear disorder", "EAR DISORDER", "Disorder ear", "diseases ear", "disease ears", "Ear Disorder", "Disease, Ear", "ear diseases", "Ear--Diseases", "disorders ear", "EAR DISORDERS", "ear disorders", "disorder ears", "diseases ears", "ear condition", "Ear Disorders", "ear; disorder", "conditions ear", "disease of ear", "Ear conditions", "ear conditions", "disorder of ear", "Disorder of ear", "disease earrings", "Otologic Disease", "Ear disorder NOS", "EAR DISORDER NOS", "disorders earing", "Disease, Otologic", "Otologic Diseases", "EAR DISORDER (NOS)", "Otological Disease", "diseases of the ear", "DISEASES OF THE EAR", "Otological Diseases", "Disease, Otological", "Disorder of ear, NOS", "ear disease or disorder", "disease (or disorder); ear", "Disorder of ear (disorder)", "disease or disorder of ear", "Disease or syndrome of ear", "disorder of ear (diagnosis)", "Unspecified disorder of ear", "Disorder of ear, unspecified", "DISEASES OF THE EAR: GENERAL TERMS", "Unspecified disorder of ear, unspecified ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of ear", "shortest_name_length": 11}
{"curie": "MONDO:0003870", "names": ["childhood brainstem astrocytoma", "Childhood Brainstem Astrocytoma", "Childhood Brain Stem Astrocytoma", "childhood brain stem astrocytoma", "pediatric brain stem astrocytic neoplasm", "childhood brain stem astrocytic neoplasm", "brain stem astrocytic neoplasm of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood brainstem astrocytoma", "shortest_name_length": 31}
{"curie": "MONDO:0002967", "names": ["tinea capitis", "scalp ringworm", "Scalp ringworm", "scalp dermatophytosis", "dermatophytosis of scalp", "Dermatophytosis of scalp", "Trichophyton rubrum tinea capitis", "dermatophytosis of scalp or beard", "dermatophytosis of scalp and beard", "Dermatophytosis of scalp and beard", "Dermatophytosis of Scalp and Beard", "tinea capitis due to Trichophyton rubrum", "Tinea capitis due to Trichophyton rubrum", "Tinea capitis caused by Trichophyton rubrum", "tinea capitis due to Trichophyton rubrum (diagnosis)", "Tinea capitis caused by Trichophyton rubrum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermatophytosis of scalp or beard", "shortest_name_length": 13}
{"curie": "MONDO:0021312", "names": ["adrenal cortex cancer", "Adrenocortical Cancer", "adrenocortical cancer", "Adrenal Cortex Cancer", "Cancer, Adrenal Cortex", "Cancer, Adrenocortical", "Adrenocortical Cancers", "Adrenal Cortex Cancers", "Cancers, Adrenocortical", "Cancers, Adrenal Cortex", "cancer of adrenal cortex", "Cancer of Adrenal Cortex", "Cancer of the Adrenal Cortex", "malignant adrenocortical tumor", "Malignant Adrenal Cortex Tumor", "malignant adrenal cortex tumor", "Malignant Adrenocortical Tumor", "Malignant adrenal cortical tumor", "Adrenal cortical tumor, malignant", "Malignant tumor of adrenal cortex", "malignant adrenal cortex neoplasm", "malignant adrenocortical neoplasm", "Malignant Tumor of Adrenal Cortex", "Malignant Adrenal Cortex Neoplasm", "Malignant adrenal cortical tumour", "malignant tumor of adrenal cortex", "Malignant Adrenocortical Neoplasm", "Adrenal cortical tumour, malignant", "tumor; adrenal cortical, malignant", "adrenal cortical; tumor, malignant", "Malignant tumour of adrenal cortex", "adrenal; cortical, tumor, malignant", "Malignant Adrenal Cortical Neoplasm", "adrenal; tumor, cortical, malignant", "malignant neoplasm of adrenal cortex", "Malignant Neoplasm of Adrenal Cortex", "Malignant neoplasm of adrenal cortex", "malignant tumor of the adrenal cortex", "Malignant Tumor of the Adrenal Cortex", "malignant neoplasm of the adrenal cortex", "Malignant Neoplasm of the Adrenal Cortex", "Malignant neoplasm of cortex of adrenal gland", "Malignant neoplasm of adrenal cortex (disorder)", "malignant neoplasm of adrenal cortex (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant tumor of adrenal cortex", "shortest_name_length": 21}
{"curie": "MONDO:0033533", "names": ["COXPD45", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 45", "combined oxidative phosphorylation deficiency 45"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation deficiency 45", "shortest_name_length": 7}
{"curie": "MONDO:0043254", "names": ["strophulus", "Strophulus", "Hebra prurigo", "Prurigo Hebra", "prurigo; Hebra", "Hebra; prurigo", "prurigo simplex", "Prurigo simplex", "Hebra's prurigo", "Prurigo, simplex", "Lichen urticatus", "Prurigo, Hebra's", "lichen urticatus", "papular urticaria", "lichen; urticatus", "Papular urticaria", "Urticaria papular", "urticatus; lichen", "Hebra's prurigo (disorder)", "Urticaria papulosa (Hebra)", "Prurigo simplex (disorder)", "prurigo simplex (diagnosis)", "Urticaria papulosa of Hebra", "Papular urticarial eruption", "urticaria papulosa of hebra", "papular urticaria (diagnosis)", "Bullous papular urticaria - type", "bullous papular urticaria - type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papular urticaria", "shortest_name_length": 10}
{"curie": "MONDO:0000259", "names": ["asymptomatic dengue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "asymptomatic dengue", "shortest_name_length": 19}
{"curie": "UMLS:C0334567", "names": ["Malignant adamantinoma", "malignant; adamantinoma", "malignant ameloblastoma", "Adamantinoma, malignant", "adamantinoma; malignant", "Malignant Ameloblastoma", "Malignant ameloblastoma", "Ameloblastoma, malignant", "ameloblastoma; malignant", "AMELOBLASTOMA, MALIGNANT", "malignant; ameloblastoma", "Metastasizing Ameloblastoma", "malignant ameloblastoma (diagnosis)", "Ameloblastoma, malignant (morphologic abnormality)", "Adamantinoma, malignant (except of Tibia and Long bones, M-92613)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Ameloblastoma", "shortest_name_length": 22}
{"curie": "UMLS:C4331348", "names": ["Stage IVC Oropharyngeal (p16-Negative) Throat Cancer", "Stage IVC Oropharyngeal (p16-Negative) Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Oropharyngeal (p16-Negative) Carcinoma AJCC v8", "shortest_name_length": 52}
{"curie": "UMLS:C5237215", "names": ["ATTR-CM", "Transthyretin Amyloid Cardiomyopathy", "Transthyretin amyloid cardiomyopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transthyretin amyloid cardiomyopathy", "shortest_name_length": 7}
{"curie": "MONDO:0006366", "names": ["Gastric Peutz-Jeghers Polyp", "Gastric Peutz-Jeghers polyp", "Peutz-Jeghers polyp of the stomach", "Peutz-Jeghers Polyp of the Stomach"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peutz-Jeghers polyp of the stomach", "shortest_name_length": 27}
{"curie": "MONDO:0030846", "names": ["SPGF48", "spermatogenic failure 48", "SPERMATOGENIC FAILURE 48"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 48", "shortest_name_length": 6}
{"curie": "MONDO:0005752", "names": ["EPIDURAL ABSCESS", "Epidural abscess", "epidural abscess", "Epidural Abscess", "abscess epidural", "abscess; epidural", "epidural; abscess", "Abscess, Epidural", "Extradural Abscess", "Extradural abscess", "abscesses epidural", "Abscess, Extradural", "extradural; abscess", "abscess; extradural", "Extradural abscess NOS", "spinal epidural abscess", "spinal extradural abscess", "Epidural abscess (disorder)", "intraspinal epidural abscess", "intraspinal extradural abscess", "extradural intraspinal abscess", "spinal epidural abscess (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidural abscess", "shortest_name_length": 16}
{"curie": "MONDO:0005250", "names": ["Villitis", "villitis", "villosity", "Villositis", "villositis", "villosities", "placental villitis", "Villitis (disorder)", "Villitis (diagnosis)", "Inflammation of chorionic villi", "placental disorders of chorion villitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "placental villitis", "shortest_name_length": 8}
{"curie": "MONDO:0017324", "names": ["ARHR", "autosomal recessive hypophosphatemic rickets", "hypophosphatemic rickets, autosomal recessive", "autosomal recessive hereditary hypophosphatemic rickets", "hereditary hypophosphatemic rickets, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive hypophosphatemic rickets", "shortest_name_length": 4}
{"curie": "MONDO:0023199", "names": ["frontonasal dysplasia phocomelic upper limbs"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontonasal dysplasia phocomelic upper limbs", "shortest_name_length": 44}
{"curie": "MONDO:0012694", "names": ["JBTS7", "JOUBERT SYNDROME 7", "Joubert Syndrome 7", "Joubert syndrome 7", "Joubert syndrome type 7", "RPGRIP1L Joubert syndrome", "Joubert syndrome caused by mutation in RPGRIP1L"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome 7", "shortest_name_length": 5}
{"curie": "MONDO:0009976", "names": ["RETINAL DEGENERATION AND EPILEPSY", "retinal degeneration and epilepsy", "Retinal Degeneration and Epilepsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal degeneration and epilepsy", "shortest_name_length": 33}
{"curie": "OMIM:601550", "names": [], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"]}
{"curie": "MONDO:0032653", "names": ["CUGS", "CARDIAC-UROGENITAL SYNDROME", "cardiac-urogenital syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiac-urogenital syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0001777", "names": ["Gonococcal cystitis", "Bladder gonorrhea - acute", "acute gonococcal cystitis", "Acute gonococcal cystitis", "gonococcal cystitis, acute", "acute gonorrhea of bladder", "Acute gonorrhea of bladder", "Bladder gonorrhoea - acute", "gonococcal cystitis (acute)", "Gonococcal cystitis (acute)", "Acute gonococcal cystitis (disorder)", "acute gonococcal cystitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute gonococcal cystitis", "shortest_name_length": 19}
{"curie": "MONDO:0002667", "names": ["gallbladder signet Ring cell carcinoma", "Gallbladder Signet-Ring Cell Carcinoma", "Gallbladder Signet Ring Cell Carcinoma", "gall bladder signet ring cell carcinoma", "signet ring cell carcinoma of gallbladder", "signet Ring cell carcinoma of gallbladder", "Signet Ring Cell Carcinoma of Gallbladder", "gallbladder signet ring cell adenocarcinoma", "Signet Ring Cell Carcinoma of the Gallbladder", "Signet Ring cell carcinoma of the gallbladder", "signet Ring cell carcinoma of the gallbladder", "signet ring cell carcinoma of gallbladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gallbladder signet ring cell adenocarcinoma", "shortest_name_length": 38}
{"curie": "UMLS:C0205866", "names": ["Compound odontoma", "Compound Odontoma", "Compound odontome", "Compound Odontomas", "odontoma; compound", "Odontoma, Compound", "compound; odontoma", "Odontomas, Compound", "Compound odontoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Odontoma, Compound", "shortest_name_length": 17}
{"curie": "MONDO:0004384", "names": ["Maxillary Sinus Inverted Papilloma", "maxillary sinus inverted papilloma", "Inverted Papilloma of Maxillary Sinus", "inverted papilloma of maxillary sinus", "Inverted Papilloma of the Maxillary Sinus", "Inverted papilloma of the maxillary sinus", "inverted papilloma of the maxillary sinus", "Maxillary Sinus Inverted Schneiderian Papilloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maxillary sinus inverted papilloma", "shortest_name_length": 34}
{"curie": "MONDO:0012508", "names": ["agammaglobulinemia, microcephaly, and severe dermatitis", "AGAMMAGLOBULINEMIA, MICROCEPHALY, AND SEVERE DERMATITIS", "Agammaglobulinemia, microcephaly, and severe dermatitis", "agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome", "Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome", "Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome", "Agammaglobulinaemia, microcephaly, craniosynostosis, severe dermatitis syndrome", "Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome (disorder)", "Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome", "shortest_name_length": 55}
{"curie": "UMLS:C3897350", "names": ["Tourettism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tourettism", "shortest_name_length": 10}
{"curie": "UMLS:C0677689", "names": ["Stage II Grade 3 Follicular Lymphoma", "Stage II Grade 3 Contiguous Follicular Lymphoma", "contiguous stage II grade 3 follicular lymphoma", "Contiguous Stage II Grade III Follicular Lymphoma", "Contiguous Grade III Follicular Lymphoma Stage II", "Stage II Contiguous Follicular Large Cell Lymphoma", "Contiguous Follicular Large Cell Lymphoma Stage II", "Contiguous Stage II Follicular Large Cell Lymphoma", "Ann Arbor Stage II Grade 3 Contiguous Follicular Lymphoma", "contiguous stage II grade III follicular large cell lymphoma", "Contiguous Stage II Grade III Follicular Large Cell Lymphoma", "Contiguous Grade III Follicular Large Cell Lymphoma Stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage II Grade 3 Contiguous Follicular Lymphoma", "shortest_name_length": 36}
{"curie": "UMLS:C0280624", "names": ["Stage I Uterine Sarcoma", "stage I uterine sarcoma", "uterine sarcoma, stage I", "Stage I Uterine Sarcoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Uterine Sarcoma AJCC v7", "shortest_name_length": 23}
{"curie": "UMLS:C0751524", "names": ["Simple Partial Status Epilepticus", "Simple partial status epilepticus", "Status Epilepticus, Simple Partial", "Simple partial status epilepticus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Simple Partial Status Epilepticus", "shortest_name_length": 33}
{"curie": "UMLS:C5238337", "names": ["BRCA-Mutated Malignant Neoplasm", "BRCA-Associated Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "BRCA-Associated Malignant Neoplasm", "shortest_name_length": 31}
{"curie": "MONDO:0010563", "names": ["BCM", "COD5", "CBBM", "S cone monochromacy", "S-cone monochromacy", "Cone monochromatism", "S cone monochromatism", "BLUE CONE MONOCHROMACY", "Blue cone monochromacy", "blue cone monochromacy", "Incomplete achromatopsia", "blue cone monochromatism", "Blue cone monochromatism", "BLUE CONE MONOCHROMATISM", "cone dystrophy 5, X-linked", "CONE DYSTROPHY 5, X-LINKED", "Atypical X-linked achromatopsia", "atypical X-linked achromatopsia", "X-linked incomplete achromatopsia", "incomplete achromatopsia X-linked", "X-linked achromatopsia incomplete", "X-chromosome-linked achromatopsia", "achromatopsia incomplete X-linked", "Blue cone monochromatism (disorder)", "blue cone monochromacy, X-linked recessive", "color blindness blue mono cone monochromatic type", "Colorblindness, Blue-Mono-Cone-Monochromatic Type", "Color blindness blue mono cone monochromatic type", "Color blindness, blue monocone monochromatic type", "colorblindness, blue-Mono-cone-monochromatic type", "color blindness, blue monocone monochromatic type", "COLORBLINDNESS, BLUE-MONO-CONE-MONOCHROMATIC TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blue cone monochromacy", "shortest_name_length": 3}
{"curie": "UMLS:C4683013", "names": ["Stage IB Eyelid Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Eyelid Carcinoma AJCC v8", "shortest_name_length": 33}
{"curie": "MONDO:0000552", "names": ["lobular carcinoma", "Lobular Carcinoma", "lobular adenocarcinoma", "Lobular Adenocarcinoma", "Lobular adenocarcinoma", "breast lobular carcinoma", "lobular breast carcinoma", "Breast Lobular Carcinoma", "Lobular Breast Carcinoma", "Lobular Carcinoma of Breast", "lobular carcinoma of breast", "Lobular Carcinoma of the Breast", "lobular carcinoma of the breast", "lobule of mammary gland carcinoma", "carcinoma of lobule of mammary gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast lobular carcinoma", "shortest_name_length": 17}
{"curie": "UMLS:C3274516", "names": ["Single Ventricle", "Single Ventricle Defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Single Ventricle Defect", "shortest_name_length": 16}
{"curie": "UMLS:C3897522", "names": ["Stage IVA Sinonasal Squamous Cell Carcinoma AJCC v7", "Stage IVA Nasal Cavity and Paranasal Sinus Squamous Cell Cancer", "Stage IVA Nasal Cavity and Paranasal Sinus Squamous Cell Carcinoma", "Stage IVA Nasal Cavity and Paranasal Sinus Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Sinonasal Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 51}
{"curie": "UMLS:C5419562", "names": ["Advanced Renal Pelvis Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Renal Pelvis Urothelial Carcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0000316", "names": ["opportunistic bacterial infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "opportunistic bacterial infectious disease", "shortest_name_length": 42}
{"curie": "MONDO:0006383", "names": ["PCDLBCL,LT", "Primary cutaneous DLBCL, leg type", "Primary cutaneous diffuse large B-cell lymphoma leg type", "Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type", "Primary cutaneous diffuse large B-cell lymphoma, leg type", "Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg-Type", "primary cutaneous diffuse large B-cell lymphoma, Leg type", "Primary cutaneous diffuse large B-cell lymphoma leg type (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary cutaneous diffuse large B-cell lymphoma, Leg type", "shortest_name_length": 10}
{"curie": "UMLS:C0007172", "names": ["Traumatic Heart Rupture", "Heart Rupture, Traumatic", "Rupture, Traumatic Heart", "Traumatic Heart Ruptures", "Traumatic Cardiac Rupture", "Heart Ruptures, Traumatic", "Ruptures, Traumatic Heart", "heart; rupture, traumatic", "Rupture, Traumatic Cardiac", "Traumatic Cardiac Ruptures", "Cardiac Rupture, Traumatic", "Cardiac Ruptures, Traumatic", "rupture; cardiac, traumatic", "Ruptures, Traumatic Cardiac"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Heart Rupture, Traumatic", "shortest_name_length": 23}
{"curie": "MONDO:0019403", "names": ["cda", "CDA", "CDA, NOS", "Congenital hypoplastic anaemia", "Congenital dyshematopoietic anemia", "Congenital Dyserythropoietic Anemia", "Anemia, congenital dyshematopoietic", "congenital dyserythropoietic anemia", "Congenital dyserythropoietic anemia", "Dyserythropoietic Anemia, Congenital", "congenital dyshaematopoietic anaemia", "dyserythropoietic anemia, congenital", "anemia, congenital dyserythropoietic", "Congenital dyshaematopoietic anaemia", "Congenital dyserythropoietic anaemia", "Dyshematopoietic anemia (congenital)", "Anemia, congenital dyserythropoietic", "Anemia, Congenital Dyserythropoietic", "Congenital Dyserythropoietic Anemias", "Anemias, Congenital Dyserythropoietic", "Anemia, Dyserythropoietic, Congenital", "Dyserythropoietic Anemias, Congenital", "Congenital dyserythropoietic anemia, NOS", "CDA - Congenital dyserythropoietic anemia", "Congenital dyserythropoietic anaemia, NOS", "CDA - Congenital dyserythropoietic anaemia", "Congenital dyserythropoietic anemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital dyserythropoietic anemia", "shortest_name_length": 3}
{"curie": "UMLS:C4684870", "names": ["Refractory Osteosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Osteosarcoma", "shortest_name_length": 23}
{"curie": "MONDO:0009770", "names": ["3MC1", "3MC SYNDROME 1", "3MC syndrome 1", "Michels syndrome", "MASP1 3MC syndrome", "3Mc syndrome type 1", "3MC syndrome type 1", "MICHELS SYNDROME, FORMERLY", "Michels syndrome, formerly", "oculopalatoskeletal syndrome", "Oculopalatoskeletal syndrome", "OCULOPALATOSKELETAL SYNDROME", "Craniosynostosis with lid anomalies", "CRANIOSYNOSTOSIS WITH LID ANOMALIES", "craniosynostosis with 51D anomalies", "craniosynostosis-lid anomalies syndrome", "3MC syndrome caused by mutation in MASP1", "clefting-ocular anterior chamber defect-lid anomalies syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "3MC syndrome 1", "shortest_name_length": 4}
{"curie": "MONDO:0019512", "names": ["heart development disease", "congenital heart malformation", "disorder of heart development", "congenital non-syndromic heart malformation", "rare congenital non-syndromic heart malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital heart malformation", "shortest_name_length": 25}
{"curie": "MONDO:0023483", "names": ["Infective myositis", "myositis infective", "infective myositis", "Myositis;infective", "Infective Myositis", "myositis; infective", "infectious myositis", "Infectious myositis", "infective; myositis", "Infectious Myositis", "Myositis, Infectious", "Infectious Myositides", "Myositides, Infectious", "Infective myositis, NOS", "Infective myositis (disorder)", "infective myositis (diagnosis)", "Infective myositis, site unspecified", "Infective myositis, unspecified site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infectious myositis", "shortest_name_length": 18}
{"curie": "MONDO:0011126", "names": ["Air", "AIR", "acute insulin response", "ACUTE INSULIN RESPONSE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute insulin response", "shortest_name_length": 3}
{"curie": "UMLS:C0854532", "names": ["myopericarditis", "Myopericarditis", "Myopericarditis (disorder)", "myopericarditis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myopericarditis", "shortest_name_length": 15}
{"curie": "MONDO:0018577", "names": ["PXE-like syndrome with retinitis pigmentosa", "pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa", "shortest_name_length": 43}
{"curie": "MONDO:0001292", "names": ["disease ans", "ANS Disease", "ans disease", "ANS disease", "dysautonomia", "ANS disorder", "diseases ans", "ANS Diseases", "ANS diseases", "disease autonomic", "autonomic disease", "Autonomic Disease", "autonomic diseases", "Autonomic Diseases", "autonomic disorder", "autonomic disorders", "AUTONOMIC DYSFUNCTION", "autonomic dysfunction", "Autonomic dysfunction", "autonomic nervous disease", "AUTONOMIC NERVOUS DISORDERS", "autonomic nervous disorders", "Disorder of vegetative system", "segmental autonomic dysfunction", "segmental autonomic dysfunctions", "autonomic disease nervous system", "autonomic dysfunction, segmental", "autonomic nervous system disease", "autonomic dysfunctions, segmental", "autonomic diseases nervous system", "Autonomic Nervous System Diseases", "autonomic nervous system disorder", "Autonomic nervous system--Diseases", "Autonomic nervous system disorders", "Autonomic Nervous System Disorders", "autonomic nervous system disorders", "Disorder of vegetative system, NOS", "autonomic disorders nervous system", "Nervous System Diseases, Autonomic", "nervous system diseases, autonomic", "AUTONOMIC NERVOUS SYSTEM DISORDERS", "disease of autonomic nervous system", "autonomic; nervous system, disorder", "nervous system; disorder, autonomic", "disorder of autonomic nervous system", "Disorder of autonomic nervous system", "nervous system diseases, sympathetic", "Disorders of autonomic nervous system", "ANS (autonomic nervous system) diseases", "ANS (Autonomic Nervous System) Diseases", "disorder of the autonomic nervous system", "AUTONOMIC NERVOUS DISORDERS: NONSPECIFIC", "Disorders of the autonomic nervous system", "central autonomic nervous system diseases", "autonomic central nervous system diseases", "DISORDERS OF THE AUTONOMIC NERVOUS SYSTEM", "Autonomic Central Nervous System Diseases", "Disorders of the Autonomic Nervous System", "Central Autonomic Nervous System Diseases", "Disorder of autonomic nervous system, NOS", "disorders of the autonomic nervous system", "Autonomic Peripheral Nervous System Diseases", "Autonomic nervous system disease or syndrome", "autonomic peripheral nervous system diseases", "autonomic nervous system disease or disorder", "Peripheral Autonomic Nervous System Diseases", "peripheral autonomic nervous system diseases", "autonomic nervous system disorder (diagnosis)", "Disorder of peripheral autonomic nervous system", "disease (or disorder); autonomic nervous system", "disease or disorder of autonomic nervous system", "Autonomic Nervous System Diseases and Syndromes", "Disorder of autonomic nervous system (disorder)", "disorder of peripheral autonomic nervous system", "Unspecified disorder of autonomic nervous system", "disease (or disorder); nervous system, autonomic", "Disorder of autonomic nervous system, unspecified", "disease (or disorder); nervous system, vegetative", "Disorder of peripheral autonomic nervous system, NOS", "Disorder of the autonomic nervous system, unspecified", "Disorder of peripheral autonomic nervous system (disorder)", "disease (or disorder); peripheral, autonomic nervous system", "Peripheral autonomic neuropathy in disorders classified elsewhere"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autonomic nervous system disorder", "shortest_name_length": 11}
{"curie": "MONDO:0002839", "names": ["Linitis Plastica", "linitis plastica", "Linitis plastica", "[M]Linitis plastica", "leather bottle stomach", "leather-bottle stomach", "Leather-bottle stomach", "linitis plastica (diagnosis)", "gastric adenocarcinoma linitis plastica", "linitis plastica (morphologic abnormality)", "Linitis plastica (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leather-bottle stomach", "shortest_name_length": 16}
{"curie": "UMLS:C4054339", "names": ["Non-Obstructed Non-Refluxing Megaureter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Obstructed Non-Refluxing Megaureter", "shortest_name_length": 39}
{"curie": "MONDO:0017919", "names": ["EEC", "BEEC", "OEIS Complex", "OEIS COMPLEX", "OEIS complex", "OEIS syndrome", "OEIS Syndrome", "Cloacal exstrophy", "Cloacal Exstrophy", "exstrophy-epispadias complex", "Omphalocele exstrophy imperforate anus", "OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS", "Omphalocele-Exstrophy-Imperforate Anus-Spinal Defects", "bladder exstrophy-epispadias-cloacal extrophy complex", "bladder exstrophy-epispadias-cloacal exstrophy complex", "Omphalocele-cloacal exstrophy-imperforate anus-spinal defect syndrome", "Omphalocele, exstrophy of the cloaca, imperforate anus, and spinal defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exstrophy-epispadias complex", "shortest_name_length": 3}
{"curie": "MONDO:0006681", "names": ["borreliosis", "Borreliosis", "Borreliosis, NOS", "Borrelia Infection", "Borrelia infection", "Borrelia Infections", "Borrelia; infection", "infection; Borrelia", "Infection, Borrelia", "Infections, Borrelia", "Borrelial infections", "Borrelia infection NOS", "Borreliosis (disorder)", "Borreliosis (diagnosis)", "Borrelia infectious disease", "Borrelia disease or disorder", "spirochetal infection Borreliosis", "Borrelia caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borrelia infectious disease", "shortest_name_length": 11}
{"curie": "MONDO:0002261", "names": ["KERATOPATHY", "keratopathy", "Keratopathy", "Keratopathy NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratopathy", "shortest_name_length": 11}
{"curie": "UMLS:C2931735", "names": ["Epidermolytic Palmoplantar Keratoderma Vorner Type", "Epidermolytic palmoplantar keratoderma Vorner type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epidermolytic palmoplantar keratoderma Vorner type", "shortest_name_length": 50}
{"curie": "MONDO:0016618", "names": ["rheumatoid factor-negative JIA without anti-nuclear antibodies", "polyarthritis without rheumatoid factor without anti-nuclear antibodies", "juvenile rheumatoid factor-negative polyarthritis without anti-nuclear antibodies", "rheumatoid factor-negative juvenile idiopathic arthritis without anti-nuclear antibodies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rheumatoid factor-negative juvenile idiopathic arthritis without anti-nuclear antibodies", "shortest_name_length": 62}
{"curie": "UMLS:C4744428", "names": ["Chest Wall Sarcoma", "Primary Thoracic Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chest Wall Sarcoma", "shortest_name_length": 18}
{"curie": "MONDO:0016063", "names": ["CD", "CS", "BZS", "BBRS", "CWS1", "RMSS", "MHAM", "Cowden Disease", "Cowden disease", "cowden disease", "Cowdens Disease", "Cowden syndrome", "Cowden Syndrome", "cowdens disease", "cowden syndrome", "cowdens syndrome", "cowden's disease", "Cowdens Syndrome", "Cowden's disease", "Cowden's Disease", "Cowden's syndrome", "cowden's syndrome", "Cowden's Syndrome", "COWDEN SYNDROME 1", "cowdens syndromes", "RILEY-SMITH SYNDROME", "PTEN hamartoma syndrome", "Lhermitte-Duclos disease", "BANNAYAN-ZONANA SYNDROME", "Cowden syndrome (disorder)", "multiple hamartoma syndrome", "Multiple hamartoma syndrome", "Multiple Hamartoma Syndrome", "Cowden syndrome (diagnosis)", "MULTIPLE HAMARTOMA SYNDROME", "Hamartoma Syndrome, Multiple", "Multiple Hamartoma Syndromes", "Hamartoma Syndromes, Multiple", "RUVALCABA-MYHRE-SMITH SYNDROME", "Ruvalcaba-Myhre-Smith Syndrome", "BANNAYAN-RILEY-RUVALCABA SYNDROME", "dysplastic gangliocytoma of cerebellum", "dysplastic Gangliocytoma of Cerebellum", "MACROCEPHALY, MULTIPLE LIPOMAS, AND HEMANGIOMATA", "MACROCEPHALY, PSEUDOPAPILLEDEMA, AND MULTIPLE HEMANGIOMATA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cowden disease", "shortest_name_length": 2}
{"curie": "UMLS:C0597124", "names": ["Obstructive asymmetric septal hypertrophy", "Obstructive Asymmetric Septal Hypertrophy", "obstructive asymmetric septal hypertrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Obstructive asymmetric septal hypertrophy", "shortest_name_length": 41}
{"curie": "MONDO:0013183", "names": ["CSNB1C", "CSNB, COMPLETE, AUTOSOMAL RECESSIVE", "CSNB, complete, autosomal recessive", "congenital stationary night blindness 1C", "TRPM1 congenital stationary night blindness", "congenital stationary night blindness type 1C", "congenital stationary night blindness - type 1c", "night blindness, congenital stationary, type 1C", "Night Blindness, Congenital Stationary, Type 1C", "NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C", "congenital stationary night blindness - type 1c (diagnosis)", "congenital stationary night blindness 1C autosomal recessive", "congenital stationary night blindness caused by mutation in TRPM1", "night blindness, congenital stationary (complete), 1C, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital stationary night blindness 1C", "shortest_name_length": 6}
{"curie": "UMLS:C0155550", "names": ["Nerve deafness", "nerve deafness", "Deafness nerve", "DEAFNESS NERVE", "Neural deafness", "neural deafness", "DEAFNESS NERVE TYPE", "neural hearing loss", "Deafness nerve type", "Neural hearing loss", "COCHLEAR NERVE DEAFNESS", "Cochlear nerve deafness", "Neural hearing loss NOS", "Nerve conduction deafness", "nerve conduction deafness", "Retrocochlear hearing loss", "Retrocochlear Hearing Loss", "Deafness, nerve conduction", "Hearing Loss, Retrocochlear", "Neural hearing loss (disorder)", "neural hearing loss (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neural hearing loss", "shortest_name_length": 14}
{"curie": "UMLS:C0750958", "names": ["Monocular Blindness", "Blindness, Monocular"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Blindness, Monocular", "shortest_name_length": 19}
{"curie": "MONDO:0012511", "names": ["PPROM", "Preterm Premature Rupture of Membrane", "Preterm Premature Rupture of Membranes", "Preterm premature rupture of membranes", "Preterm Premature Rupture of the Membranes", "PRETERM PREMATURE RUPTURE OF THE MEMBRANES", "preterm premature rupture of the membranes", "Preterm premature rupture of membranes (PPROM)", "PPROM - Preterm premature rupture of membranes", "Preterm premature rupture of membranes (disorder)", "preterm premature rupture of the membranes, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "preterm premature rupture of the membranes", "shortest_name_length": 5}
{"curie": "MONDO:0006463", "names": ["Mucoepidermoid Thyroid Carcinoma", "mucoepidermoid thyroid carcinoma", "Thyroid Gland Mucoepidermoid Carcinoma", "Mucoepidermoid Thyroid Gland Carcinoma", "thyroid gland mucoepidermoid carcinoma", "mucoepidermoid thyroid gland carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid gland mucoepidermoid carcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C1336453", "names": ["stage I extragonadal non-seminomatous germ cell tumor", "Stage I Extragonadal Non-Seminomatous Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Extragonadal Non-Seminomatous Germ Cell Tumor", "shortest_name_length": 53}
{"curie": "MONDO:0030697", "names": ["MYP28", "myopia 28, autosomal recessive", "MYOPIA 28, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopia 28, autosomal recessive", "shortest_name_length": 5}
{"curie": "MONDO:0024639", "names": ["gastric EC cell serotonin-producing NET", "Gastric EC Cell Serotonin-Producing NET", "Gastric EC-Cell Serotonin-Producing Neuroendocrine Tumor", "gastric EC-cell serotonin-producing neuroendocrine tumor", "gastric enterochromaffin cell serotonin-producing neuroendocrine tumor", "Gastric Enterochromaffin Cell Serotonin-Producing Neuroendocrine Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric enterochromaffin cell serotonin-producing neuroendocrine tumor", "shortest_name_length": 39}
{"curie": "UMLS:C0270994", "names": ["steroid myopathy", "Steroid Myopathy", "Steroid myopathy", "Myopathy steroid", "myopathy steroids", "myopathies steroid", "Myopathy steroid-induced", "Steroid-induced myopathy", "Steroid-induced myopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Steroid-induced myopathy", "shortest_name_length": 16}
{"curie": "MONDO:0008542", "names": ["TOF", "tetralogy fallot", "Fallot Tetralogy", "fallot tetralogy", "TETRALOGY FALLOT", "Fallot tetralogy", "Fallots Tetralogy", "tetralogy; Fallot", "fallots tetralogy", "Tetralogy, Fallot", "Fallot; tetralogy", "Tetralogy, Fallots", "fallot's tetralogy", "Fallot's Tetralogy", "Fallot's tetralogy", "tetralogy of fallot", "Tetralogy of Fallot", "Fallot tetralogy of", "tetralogy of FALLOT", "tetralogy of Fallot", "Tetrology of fallot", "Tetralogy, Fallot's", "Tetralogy of fallot", "FALLOT TETRALOGY OF", "TETRALOGY OF FALLOT", "fallot of tetralogy", "TOF - Tetralogy of Fallot", "Tetralogy of Fallot (disorder)", "tetralogy of Fallot (diagnosis)", "Subpulmonic stenosis, ventricular septal defect, overriding aorta, AND right ventricular hypertrophy", "Subpulmonic stenosis, ventricular septal defect, overriding aorta, and right ventricular hypertrophy", "Ventricular septal defect with pulmonary stenosis or atresia, dextraposition of aorta, and hypertrophy of right ventricle", "ventricular septal defect with pulmonary stenosis or atresia, dextraposition of aorta, and hypertrophy of right ventricle"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tetralogy of fallot", "shortest_name_length": 3}
{"curie": "MONDO:0019544", "names": ["COCAINE INTOXICATION", "cocaine intoxication", "Cocaine intoxication", "intoxication; cocaine", "cocaine; intoxication", "Cocaine intoxication (disorder)", "cocaine intoxication (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cocaine intoxication", "shortest_name_length": 20}
{"curie": "MONDO:0044647", "names": ["kyphosis-lateral tongue atrophy-myofibrillar myopathy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kyphosis-lateral tongue atrophy-myofibrillar myopathy syndrome", "shortest_name_length": 62}
{"curie": "MONDO:0010355", "names": ["MRXSJ", "MRXSCJ", "syndromic X-linked mental retardation JARID1C-related", "mental retardation, X-linked, syndromic, JARID1C-related", "Mental Retardation, X-Linked, Syndromic, Jarid1c-Related", "MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED", "syndromic X-linked intellectual disability JARID1C-related", "MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE", "mental retardation, X-linked, syndromic, Claes-Jensen type", "syndromic X-linked intellectual disability Claes-Jensen type", "intellectual disability, X-linked, syndromic, JARID1C-related", "intellectual disability, X-linked, syndromic, Claes-Jensen type", "syndromic X-linked intellectual disability due to JARID1C mutation", "Syndromic X-linked intellectual disability due to JARID1C mutation", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE", "intellectual developmental disorder, X-linked syndromic, Claes-Jensen type, X-linked recessive", "Syndromic X-linked intellectual disability due to jumonji at-rich interactive domain 1c mutation", "Syndromic X-linked intellectual disability due to JARID1C (jumonji at-rich interactive domain 1c) mutation", "Syndromic X-linked intellectual disability due to jumonji at-rich interactive domain 1c mutation (disorder)", "Syndromic X-linked intellectual disability due to jumonji at-rich interactive domain 1c mutation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic X-linked intellectual disability Claes-Jensen type", "shortest_name_length": 5}
{"curie": "UMLS:C3272423", "names": ["Gastric Synovial Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Synovial Sarcoma", "shortest_name_length": 24}
{"curie": "MONDO:0019786", "names": ["severe intellectual disability-epilepsy-anal anomalies-distal phalangeal hypoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe intellectual disability-epilepsy-anal anomalies-distal phalangeal hypoplasia", "shortest_name_length": 83}
{"curie": "UMLS:C5419185", "names": ["Metastatic Cutaneous Squamous Cell Carcinoma of the Head and Neck"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Cutaneous Squamous Cell Carcinoma of the Head and Neck", "shortest_name_length": 65}
{"curie": "MONDO:0004593", "names": ["Bartholin cyst", "Bartholin Cyst", "bartholin cyst", "Cyst;Bartholin", "BARTHOLIN CYST", "cyst; Bartholin", "bartholin cysts", "Bartholin; cyst", "bartholins cyst", "Bartholin's cyst", "bartholin's cyst", "Bartholin's Cyst", "bartholin's cysts", "gl.Bartholin; cyst", "Bartholin duct cyst", "Bartholin Duct Cyst", "bartholin cyst gland", "bartholin gland cyst", "Bartholin gland cyst", "Bartholin Gland Cyst", "BARTHOLIN GLAND CYST", "bartholin's duct cyst", "bartholin cysts gland", "Bartholin's duct cyst", "BARTHOLIN GLAND, CYST", "bartholins cyst gland", "BARTHOLIN'S GLAND CYST", "Bartholin's gland cyst", "bartholin cyst/abscess", "abscess bartholin cyst", "bartholin's gland cyst", "cyst; bartholin's gland", "bartholin's cysts gland", "abscesses bartholin cyst", "bartholins's cysts gland", "cyst of Bartholin's gland", "Cyst of Bartholin's gland", "Bartholin's gland duct cyst", "Cyst of Bartholin gland duct", "cyst of Bartholin's gland duct", "Cyst of Bartholin's gland duct", "Bartholin duct cyst (diagnosis)", "Bartholin gland cyst (diagnosis)", "Cyst of Bartholin's gland duct (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bartholin duct cyst", "shortest_name_length": 14}
{"curie": "MONDO:0006231", "names": ["Hamartomatous Polyp", "Hamartomatous polyp", "Hamartomatous polyps", "Peutz-Jeghers' polyp", "Hamartomatous polyposis", "Gastrointestinal hamartoma", "gastrointestinal hamartoma", "Gastrointestinal Hamartoma", "Gastrointestinal hamartomatous polyps", "Hamartomatous polyp (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastrointestinal hamartoma", "shortest_name_length": 19}
{"curie": "MONDO:0024988", "names": ["sex cord-stromal benign neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sex cord-stromal benign neoplasm", "shortest_name_length": 32}
{"curie": "MONDO:0010738", "names": ["SMDXL", "X-linked spondylometaphyseal dysplasia", "spondylometaphyseal dysplasia X-linked", "spondylometaphyseal dysplasia, X-linked", "SPONDYLOMETAPHYSEAL DYSPLASIA, X-LINKED", "Spondylometaphyseal Dysplasia, X-Linked", "Spondylometaphyseal dysplasia Golden type", "spondylometaphyseal dysplasia, Golden type", "Spondylometaphyseal dysplasia, Golden type", "spondylometaphyseal dysplasia Richmond type", "spondylometaphyseal dysplasia, Richmond type", "SPONDYLOMETAPHYSEAL DYSPLASIA, RICHMOND TYPE", "Spondylometaphyseal Dysplasia, Richmond Type", "Spondylometaphyseal dysplasia Golden type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondylometaphyseal dysplasia, Golden type", "shortest_name_length": 5}
{"curie": "UMLS:C4331323", "names": ["Stage II Major Salivary Gland Cancer", "Stage II Major Salivary Gland Cancer AJCC v8", "Stage II Major Salivary Gland Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Major Salivary Gland Cancer AJCC v8", "shortest_name_length": 36}
{"curie": "UMLS:C0278722", "names": ["Stage I Multiple Myeloma", "Multiple Myeloma Stage I", "stage I multiple myeloma", "multiple myeloma, stage I", "DS Stage I Multiple Myeloma", "Stage I Plasma Cell Myeloma", "plasma cell neoplasm, stage I", "DS Stage I Plasma Cell Myeloma", "Durie/Salmon Stage I Multiple Myeloma", "Durie/Salmon Stage I Plasma Cell Myeloma", "DS Stage I Multiple Myeloma/Plasma Cell Myeloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DS Stage I Plasma Cell Myeloma", "shortest_name_length": 24}
{"curie": "MONDO:0014633", "names": ["MAE", "mae", "Myoclonic-Atonic Seizure", "Myoclonic-atonic epilepsy", "MYOCLONIC-ATONIC EPILEPSY", "myoclonic-atonic epilepsy", "Myoclonic-Atonic Epilepsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myoclonic-atonic epilepsy", "shortest_name_length": 3}
{"curie": "UMLS:C0036210", "names": ["Musculoskeletal cancer", "musculoskeletal cancer", "Neoplasm malig;musculoskeletal", "Malignant Musculoskeletal Neoplasm", "Malignant neoplasm musculoskeletal", "malignant neosplasm of the musculoskeletal system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant neoplasm musculoskeletal", "shortest_name_length": 22}
{"curie": "MONDO:0009208", "names": ["faciothoracogenital syndrome", "FACIOTHORACOGENITAL SYNDROME", "Faciothoracogenital Syndrome", "facio thoraco genital syndrome", "Facio thoraco genital syndrome", "Congenital anomalies, involving mainly the face, thorax, and genitalia", "congenital anomalies, involving mainly the face, thorax, and genitalia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "faciothoracogenital syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0002109", "names": ["Pituitary cancer", "pituitary cancer", "pituitary neoplasm", "pituitary gland cancer", "cancer pituitary gland", "Pituitary gland neoplasm", "pituitary gland neoplasm", "Cancer of pituitary gland", "Malignant pituitary tumor", "Pituitary tumor malignant", "cancer of pituitary gland", "Malignant Pituitary Tumor", "malignant pituitary tumor", "pituitary tumor, malignant", "Pituitary Tumor, Malignant", "Pituitary tumour malignant", "Malignant pituitary tumour", "neoplasm of pituitary gland", "malignant Pituitary neoplasm", "Malignant Tumor of Pituitary", "malignant pituitary neoplasm", "malignant tumor of pituitary", "Malignant Pituitary Neoplasm", "Pituitary tumor malignant NOS", "Pituitary Neoplasms, Malignant", "CA - Cancer of pituitary gland", "Pituitary tumour malignant NOS", "pituitary neoplasms, malignant", "malignant pituitary gland tumor", "Malignant Neoplasm of Pituitary", "Malignant Pituitary Gland Tumor", "malignant neoplasm of pituitary", "Malignant Tumor of the Pituitary", "malignant tumor of the pituitary", "Malignant Pituitary Gland Neoplasm", "malignant tumor of pituitary gland", "Malignant tumor of pituitary gland", "Malignant Tumor of Pituitary Gland", "malignant pituitary gland neoplasm", "Malignant Neoplasm of the Pituitary", "malignant neoplasm of the pituitary", "Malignant tumour of pituitary gland", "malignant neoplasm of pituitary gland", "Malignant neoplasm of pituitary gland", "Malignant Neoplasm of Pituitary Gland", "malignant tumor of the pituitary gland", "Malignant Tumor of the Pituitary Gland", "malignant neoplasm of the pituitary gland", "Malignant Neoplasm of the Pituitary Gland", "Malignant tumor of pituitary gland (disorder)", "malignant neoplasm of pituitary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pituitary cancer", "shortest_name_length": 16}
{"curie": "MONDO:0024266", "names": ["PDA3", "PATENT DUCTUS ARTERIOSUS 3", "patent ductus arteriosus 3", "PRDM6 patent ductus arteriosus", "patent ductus arteriosus caused by mutation in PRDM6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "patent ductus arteriosus 3", "shortest_name_length": 4}
{"curie": "MONDO:0014432", "names": ["BBS", "BBS2", "Bardet-Biedl syndrome", "Bardet-Biedl syndrome 2", "BARDET-BIEDL SYNDROME 2", "BBS2 Bardet-Biedl syndrome", "Bardet-Biedl syndrome type 2", "Bardet-Biedl syndrome 2 (disorder)", "Bardet-Biedl syndrome caused by mutation in BBS2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bardet-Biedl syndrome 2", "shortest_name_length": 3}
{"curie": "UMLS:C0156287", "names": ["Urethral Prolapse", "Prolapsed urethral mucosa", "prolapsed urethral mucosa", "Prolapse of urethral mucosa", "Prolapse of urethral mucosa (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prolapsed urethral mucosa", "shortest_name_length": 17}
{"curie": "MONDO:0009556", "names": ["MCD deficiency", "Malonicaciduria", "malonic aciduria", "malonic acidemia", "Malonic aciduria", "Malonic aciduria (disorder)", "malonic aciduria (diagnosis)", "MALONYL-CoA DECARBOXYLASE DEFICIENCY", "Malonyl-CoA decarboxylase deficiency", "malonyl-CoA decarboxylase deficiency", "Deficiency of malonyl-CoA decarboxylase", "Malonyl-Coenzyme A Decarboxylase Deficiency", "Deficiency of malonyl-coenzyme A decarboxylase", "Deficiency of malonyl-coenzyme A decarboxylase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malonic aciduria", "shortest_name_length": 14}
{"curie": "UMLS:C1332254", "names": ["Ampulla of Vater Undifferentiated Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ampulla of Vater Undifferentiated Carcinoma", "shortest_name_length": 43}
{"curie": "UMLS:C4511178", "names": ["TCACC", "Thymic carcinoma with adenoid cystic carcinoma-like features", "Thymic Carcinoma with Adenoid Cystic Carcinoma-Like Features", "Thymic carcinoma with adenoid cystic carcinoma-like features (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thymic carcinoma with adenoid cystic carcinoma-like features", "shortest_name_length": 5}
{"curie": "MONDO:0017080", "names": ["Notoencephalocele", "Notoencephaloceles", "Occipital Encephalocele", "Occipital encephalocele", "occipital encephalocele", "Posterior encephalocele", "encephalocele occipital", "encephalocele; occipital", "Encephalocele, Occipital", "occipital; encephalocele", "Encephalocele, occipital", "Occipital Encephaloceles", "Encephaloceles, Occipital", "Occipital meningoencephalocele", "Occipital encephalocele (disorder)", "occipital encephalocele (diagnosis)", "Brain tissue sticks out through back of skull"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "occipital encephalocele", "shortest_name_length": 17}
{"curie": "MONDO:0010201", "names": ["WNCHRS", "NOA syndrome", "Winchester disease", "Winchester Syndrome", "Winchester syndrome", "WINCHESTER SYNDROME", "Torg-Winchester Syndrome", "Torg Winchester syndrome", "Al-Qeel Sewairi syndrome", "Winchester-Grossman disease", "Winchester-Grossman syndrome", "Winchester syndrome (disorder)", "Winchester syndrome (diagnosis)", "nodulosis arthropathy osteolysis syndrome", "multicentric osteolysis, nodulosis and arthropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Winchester syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0002155", "names": ["CHOLECYSTITIS", "Cholecystitis", "cholecystitis", "Cholecystitis NOS", "Cholecystitis, NOS", "acute cholecystitis", "Inflamed gallbladder", "Cholecystitis chronic", "cholecystitis chronic", "chronic cholecystitis", "CHOLECYSTITIS CHRONIC", "Chronic cholecystitis", "Chronic Cholecystitis", "CHOLECYSTITIS, CHRONIC", "chronic; cholecystitis", "cholecystitis; chronic", "gallstone cholecystitis", "Gallbladder inflammation", "gallbladder inflammation", "Cholecystitis (disorder)", "Gallbladder Inflammation", "Inflammation gallbladder", "acalculous cholecystitis", "INFLAMMATION GALL BLADDER", "gallbladder; inflammation", "Cholecystitis chronic NOS", "Inflammation, Gallbladder", "gall bladder inflammation", "GALL BLADDER INFLAMMATION", "cholecystitis (diagnosis)", "inflammation; gallbladder", "Chronic cholecystitis, NOS", "Cholecystitis, unspecified", "inflammation of gall bladder", "acute on chronic cholecystitis", "Chronic calculous cholecystitis", "acute and chronic cholecystitis", "Chronic cholecystitis (disorder)", "chronic cholecystitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholecystitis", "shortest_name_length": 13}
{"curie": "MONDO:0002782", "names": ["Cranial Nerve Palsy", "cranial nerve palsy", "CRANIAL NERVE PALSY", "Cranial nerve palsy", "cranial nerves palsy", "Palsy, Cranial Nerve", "Paresis cranial nerve", "Cranial nerve palsies", "Cranial nerve paresis", "Cranial Nerve Palsies", "cranial nerve palsies", "Palsies, Cranial Nerve", "Cranial Nerve Paralysis", "Cranial nerve paralysis", "cranial nerve paralysis", "CRANIAL NERVE PARALYSIS", "Cranial nerve Paralysis", "Paresis cranial nerve NOS", "Paralysis of cranial nerve NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cranial nerve palsy", "shortest_name_length": 19}
{"curie": "MONDO:0013041", "names": ["aHUS3", "AHUS3", "aHUS with I factor anomaly", "aHUS, susceptibility to, 3", "AHUS, SUSCEPTIBILITY TO, 3", "D-HUS with I factor anomaly", "atypical HUS with I factor anomaly", "susceptibility to atypical hemolytic uremic syndrome 3", "atypical hemolytic-uremic syndrome with I factor anomaly", "HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3", "hemolytic uremic syndrome, atypical, susceptibility to, 3", "hemolytic uremic syndrome, atypical, susceptibility to, type 3", "hemolytic-uremic syndrome without diarrhea with I factor anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical hemolytic-uremic syndrome with I factor anomaly", "shortest_name_length": 5}
{"curie": "UMLS:C4725026", "names": ["Refractory Mixed Phenotype Acute Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Mixed Phenotype Acute Leukemia", "shortest_name_length": 41}
{"curie": "MONDO:0011601", "names": ["NICCD", "Neonatal-onset citrullinemia type 2", "neonatal-onset citrullinemia type 2", "neonatal-onset type 2 citrullinemia", "neonatal-onset type II citrullinemia", "neonatal-onset citrullinemia type II", "Neonatal-onset citrullinemia type II", "CITRULLINEMIA, TYPE II, NEONATAL-ONSET", "citrullinemia, type II, neonatal-onset", "Citrullinemia, Type II, Neonatal-Onset", "neonatal intrahepatic cholestasis due to citrin deficiency", "Neonatal intrahepatic cholestasis due to citrin deficiency", "Neonatal intrahepatic cholestasis caused by citrin deficiency", "neonatal intrahepatic cholestasis caused by citrin deficiency", "CHOLESTASIS, NEONATAL INTRAHEPATIC, CAUSED BY CITRIN DEFICIENCY", "Cholestasis, Neonatal Intrahepatic, caused by Citrin Deficiency", "cholestasis, neonatal intrahepatic, caused by citrin deficiency", "Neonatal intrahepatic cholestasis due to citrin deficiency (disorder)", "CITRULLINEMIA, TYPE II, NEONATAL-ONSET, WITH OR WITHOUT FAILURE TO THRIVE AND DYSLIPIDEMIA", "citrullinemia, type II, neonatal-onset, with or without failure to thrive and dyslipidemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal intrahepatic cholestasis due to citrin deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0021061", "names": ["Neurofibromatosis", "neurofibromatosis", "Neurofibromatosis, NOS", "neurofibromatosis type 2", "neurofibromatosis type 4", "central Neurofibromatosis", "neurofibromatosis type IV", "von Reklinghausen disease", "Acoustic neurofibromatosis", "neurofibromatosis syndrome", "Neurofibromatosis Syndrome", "acoustic neurofibromatosis", "peripheral Neurofibromatosis", "Recklinghausen's neurofibromatosis", "type IV neurofibromatosis of riccardi"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurofibromatosis", "shortest_name_length": 17}
{"curie": "MONDO:0008072", "names": ["Igan", "IGAN1", "berger disease", "nephritis, IgA type", "glomerulonephritis, IgA", "IgA NEPHROPATHY, SUSCEPTIBILITY TO, 1", "IgA nephropathy, susceptibility to, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IgA nephropathy, susceptibility to, 1", "shortest_name_length": 4}
{"curie": "MONDO:0002654", "names": ["uterus disease", "disease uterus", "Uterine disease", "Uterine Disease", "uterine disease", "diseases uterus", "uterus disorder", "uterine diseases", "diseases uterine", "uterus; disorder", "Uterus--Diseases", "Uterine Disorder", "Uterine disorder", "Disease, Uterine", "uterine disorder", "UTERINE DISORDER", "disorders uterus", "Uterine Diseases", "uterine disorders", "disorders uterine", "disease of uterus", "Diseases, Uterine", "Disorder of uterus", "disorder of uterus", "UTERINE DISORDER NOS", "Uterine disease, NOS", "Uterine disorder NOS", "Uterine disorder, NOS", "DISORDER UTERINE (NOS)", "UTERINE DISORDER (NOS)", "Disease of uterus, NOS", "Disorder of uterus NOS", "nos disorder of uterus", "uterus disease or disorder", "Uterine disease or syndrome", "disease or disorder of uterus", "uterine disorders (diagnosis)", "Disorder of uterus (disorder)", "Disease or syndrome of uterus", "Unspecified disorder of uterus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine disorder", "shortest_name_length": 14}
{"curie": "UMLS:C0522560", "names": ["track marks", "Track marks", "Track Marks", "TRACK MARKS", "needle track", "Needle track", "needle tracks", "needle track marks", "Needle track marks", "Needle Track Marks", "needle tracks (physical finding)", "Needle track (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Needle track", "shortest_name_length": 11}
{"curie": "MONDO:0020284", "names": ["heart position anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heart position anomaly", "shortest_name_length": 22}
{"curie": "UMLS:C5421304", "names": ["Advanced Endometrioid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Endometrioid Adenocarcinoma", "shortest_name_length": 36}
{"curie": "MONDO:0003311", "names": ["endometrial stroma tumor", "Endometrial stromal tumor", "Endometrial Stromal Tumor", "endometrial stromal tumor", "Stromal Tumor, Endometrial", "Tumor, Endometrial Stromal", "Endometrial Stromal Tumors", "Endometrial stromal tumour", "Stromal Tumors, Endometrial", "tumor of endometrial stroma", "endometrial stroma neoplasm", "Tumors, Endometrial Stromal", "endometrial Stromal neoplasm", "endometrial stromal neoplasm", "neoplasm of endometrial stroma", "Endometrial stromal tumor, NOS", "Endometrial stromal tumour, NOS", "Endometrial stromal tumor (disorder)", "Endometrial stromal tumor of uncertain behavior", "Endometrial stromal tumour of uncertain behaviour", "endometrial stromal tumor (morphologic abnormality)", "Endometrial stromal tumor of uncertain behavior (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometrial stromal tumor", "shortest_name_length": 24}
{"curie": "UMLS:C0861222", "names": ["Stage IV Centroblastic Lymphoma", "Centroblastic lymphoma stage IV", "Ann Arbor Stage IV Centroblastic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Centroblastic lymphoma stage IV", "shortest_name_length": 31}
{"curie": "MONDO:0000297", "names": ["baylisascariasis", "Baylisascariasis", "Ascaridida Infection", "Ascaridida Infections", "Infection, Ascaridida", "Infections, Ascaridida", "Baylisascaris Infection", "Baylisascaris Infections", "Infection, Baylisascaris", "Infections, Baylisascaris", "Infection by Baylisascaris", "raccoon roundworm infection", "Raccoon Roundworm Infection", "Roundworm Infection, Raccoon", "Raccoon Roundworm Infections", "Infection, Raccoon Roundworm", "Roundworm Infections, Raccoon", "Infection by Baylisascaris, NOS", "Infection caused by Baylisascaris", "Baylisascaris procyonis infectious disease", "Baylisascaris procyonis disease or disorder", "Infection caused by Baylisascaris (disorder)", "Baylisascaris procyonis caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "baylisascariasis", "shortest_name_length": 16}
{"curie": "UMLS:C0948782", "names": ["Uterine cramps", "uterine cramps", "cramping uterine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine cramps", "shortest_name_length": 14}
{"curie": "UMLS:C4330181", "names": ["HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma by AJCC v8 Stage", "shortest_name_length": 68}
{"curie": "MONDO:0003140", "names": ["glomerulonephritis immune-complex", "GLOMERULONEPHRITIS IMMUNE COMPLEX", "Immune Complex Glomerulonephritis", "immune-complex glomerulonephritis", "immune Complex glomerulonephritis", "Immune-complex glomerulonephritis", "complex glomerulonephritis immune", "Immune complex glomerulonephritis", "immune complex; glomerulonephritis", "glomerulonephritis; immune complex", "Immune-complex glomerulonephritis (disorder)", "Immune-complex glomerulonephritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immune-complex glomerulonephritis", "shortest_name_length": 33}
{"curie": "UMLS:C0334338", "names": ["EBT/APET", "Endometrioid tumor, borderline", "Endometrioid tumour, borderline", "Borderline Endometrioid Cystadenoma", "Borderline Endometrioid Adenofibroma", "Ovarian Endometrioid Borderline Tumor", "Borderline Ovarian Endometrioid Tumor", "Borderline Endometrioid Tumor of Ovary", "Borderline Ovarian Endometrioid Neoplasm", "Proliferating Ovarian Endometrioid Tumor", "Ovarian Endometrioid Borderline Neoplasm", "Atypical proliferative endometrioid tumor", "Proliferating Endometrioid Tumor of Ovary", "Borderline Endometrioid Neoplasm of Ovary", "Borderline Endometrioid Tumor of the Ovary", "Atypical proliferative endometrioid tumour", "Endometrioid adenoma, borderline malignancy", "Proliferating Ovarian Endometrioid Neoplasm", "Proliferating Endometrioid Neoplasm of Ovary", "Endometrioid adenoma - borderline malignancy", "Borderline Endometrioid Neoplasm of the Ovary", "Endometrioid tumor of low malignant potential", "Proliferating Endometrioid Tumor of the Ovary", "Endometrioid Tumor of Low Malignant Potential", "Borderline Malignancy Endometrioid Cystadenoma", "Endometrioid tumour of low malignant potential", "Endometrioid cystadenoma, borderline malignancy", "Borderline Malignancy Endometrioid Adenofibroma", "Endometrioid adenofibroma, borderline malignancy", "Endometrioid Neoplasm of Low Malignant Potential", "Endometrioid cystadenoma - borderline malignancy", "Proliferating Endometrioid Neoplasm of the Ovary", "borderline malignancy; endometrioid adenofibroma", "endometrioid; adenofibroma, borderline malignancy", "Low Malignancy Potential Endometrioid Cystadenoma", "adenofibroma; endometrioid, borderline malignancy", "Endometrioid adenofibroma - borderline malignancy", "Low Malignant Potential Ovarian Endometrioid Tumor", "Low Malignant Potential Endometrioid Tumor of Ovary", "Endometrioid cystadenofibroma, borderline malignancy", "borderline malignancy; endometrioid cystadenofibroma", "cystadenofibroma; endometrioid, borderline malignancy", "Ovarian Endometrioid Tumor of Low Malignant Potential", "Low Malignant Potential Ovarian Endometrioid Neoplasm", "endometrioid; cystadenofibroma, borderline malignancy", "Endometrioid cystadenofibroma - borderline malignancy", "Low Malignant Potential Endometrioid Neoplasm of Ovary", "Ovarian Endometrioid Tumor with Proliferating Activity", "ovarian endometrioid tumor with proliferating activity", "Low Malignant Potential Endometrioid Tumor of the Ovary", "endometrioid tumor with proliferating activity, ovarian", "Endometrioid Tumor with Proliferating Activity, Ovarian", "Ovarian Endometrioid Neoplasm of Low Malignant Potential", "Ovarian Endometrioid Neoplasm with Proliferating Activity", "Low Malignant Potential Endometrioid Neoplasm of the Ovary", "Endometrioid Neoplasm with Proliferating Activity, Ovarian", "Endometrioid adenoma, borderline malignancy (morphologic abnormality)", "Endometrioid adenofibroma, borderline malignancy (morphologic abnormality)", "Borderline Ovarian Endometrioid Tumor/Atypical Proliferative Ovarian Endometrioid Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Ovarian Endometrioid Tumor/Atypical Proliferative Ovarian Endometrioid Tumor", "shortest_name_length": 8}
{"curie": "MONDO:0012483", "names": ["CORD11", "Cone-Rod Dystrophy 11", "CONE-ROD DYSTROPHY 11", "cone-rod dystrophy 11", "RAX2 cone-rod dystrophy", "cone-rod dystrophy type 11", "cone-rod dystrophy caused by mutation in RAX2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cone-rod dystrophy 11", "shortest_name_length": 6}
{"curie": "UMLS:C4289807", "names": ["Cervical Yolk Sac Tumor", "Cervical Endodermal Sinus Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Yolk Sac Tumor", "shortest_name_length": 23}
{"curie": "UMLS:C5556432", "names": ["Mismatch Repair-Deficient Endometrial Endometrioid Carcinoma", "Mismatch Repair-Deficient Endometrial Endometrioid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mismatch Repair-Deficient Endometrial Endometrioid Adenocarcinoma", "shortest_name_length": 60}
{"curie": "MONDO:0018952", "names": ["Argyria", "ARGYRIA", "argyria", "Argyrias", "argyrosis", "Argyrosis", "Silver staining", "SILVER POISONING", "silver poisoning", "Silver poisoning", "poisoning by silver", "Deposition of silver", "Silver poisoning syndrome", "Argyria (qualifier value)", "Silver poisoning (disorder)", "poisoning by silver (diagnosis)", "Deposition of silver (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "argyria", "shortest_name_length": 7}
{"curie": "MONDO:0013172", "names": ["CDCBM8", "Polymicrogyria With Optic Nerve Hypoplasia", "Polymicrogyria with optic nerve hypoplasia", "polymicrogyria with optic nerve hypoplasia", "Polymicrogyria with optic nerve hypoplasia (disorder)", "polymicrogyria with optic nerve hypoplasia (diagnosis)", "cortical dysplasia, Complex, with Other brain malformations 8", "cortical dysplasia, complex, with other brain malformations 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polymicrogyria with optic nerve hypoplasia", "shortest_name_length": 6}
{"curie": "UMLS:C0241832", "names": ["INSUFFICIENCY CEREBROVASCULAR", "Insufficiency;cerebrovascular", "Cerebral Artery Insufficiency", "Insufficiency cerebrovascular", "CEREBROVASCULAR INSUFFICIENCY", "Cerebrovascular insufficiency", "cerebrovascular insufficiency", "Cerebrovascular Insufficiency", "insufficiency; cerebrovascular", "cerebrovascular; insufficiency", "Insufficiency, Cerebrovascular", "Cerebrovascular Insufficiencies", "Cerebral Vascular Insufficiency", "cerebral vascular insufficiency", "Insufficiencies, Cerebrovascular"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebrovascular Insufficiency", "shortest_name_length": 29}
{"curie": "UMLS:C0001548", "names": ["Brief depressive adjustment reaction", "Brief depressive adjustment reaction (disorder)", "Brief depressive adjustment reaction (diagnosis)", "Adjustment Reaction with Brief Depressive Reaction", "Adjustment reaction with brief depressive reaction", "adjustment disorder with depressed mood brief reaction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brief depressive adjustment reaction", "shortest_name_length": 36}
{"curie": "MONDO:0010532", "names": ["Amcx1", "AMCX1", "SMAX2", "XLSMA", "Xlsma", "Smax2", "AMC, distal, X-linked", "AMC, DISTAL, X-LINKED", "arthrogryposis, X-linked, type 1", "Arthrogryposis, X-Linked, Type I", "ARTHROGRYPOSIS, X-LINKED, TYPE I", "X-linked spinal muscular atrophy 2", "Spinal Muscular Atrophy, X-Linked 2", "spinal muscular atrophy, X-linked 2", "SPINAL MUSCULAR ATROPHY, X-LINKED 2", "X-linked spinal muscular atrophy type 2", "spinal muscular atrophy, X-linked type 2", "Spinal muscular atrophy with arthrogryposis", "SPINAL MUSCULAR ATROPHY, INFANTILE X-LINKED", "spinal muscular atrophy, infantile X-linked", "Spinal Muscular Atrophy, Infantile X-Linked", "spinal muscular atrophy with arthrogryposis", "infantile-onset X-linked spinal muscular atrophy", "Infantile-onset X-linked spinal muscular atrophy", "spinal muscular atrophy, X-linked lethal infantile", "X-linked distal arthrogryposis multiplex congenita", "SPINAL MUSCULAR ATROPHY, X-LINKED LETHAL INFANTILE", "Spinal Muscular Atrophy, X-Linked Lethal Infantile", "ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, X-LINKED", "arthrogryposis multiplex congenita, distal, X-linked", "Arthrogryposis multiplex congenita, distal, X-linked", "X-linked distal arthrogryposis multiplex congenita (disorder)", "spinal muscular atrophy, X-linked 2, infantile, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile-onset X-linked spinal muscular atrophy", "shortest_name_length": 5}
{"curie": "MONDO:0040870", "names": ["primary polydipsia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary polydipsia", "shortest_name_length": 18}
{"curie": "UMLS:C1336832", "names": ["Tubular Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tubular Neoplasm", "shortest_name_length": 16}
{"curie": "MONDO:0013002", "names": ["CORD9", "cone-rod dystrophy 9", "CONE-ROD DYSTROPHY 9", "ADAM9 cone-rod dystrophy", "cone-rod dystrophy type 9", "cone-rod dystrophy caused by mutation in ADAM9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cone-rod dystrophy 9", "shortest_name_length": 5}
{"curie": "MONDO:0012771", "names": ["ASRT7", "CHI3L1 inherited susceptibility to asthma", "asthma-RELATED traits, susceptibility to, 7", "ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 7", "asthma-related traits, susceptibility to, 7", "asthma-related traits, susceptibility to, type 7", "inherited susceptibility to asthma caused by mutation in CHI3L1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "asthma-related traits, susceptibility to, 7", "shortest_name_length": 5}
{"curie": "UMLS:C5206794", "names": ["Refractory Biliary Tract Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Biliary Tract Carcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0016856", "names": ["Mowat-Wilson syndrome due to a ZEB2 point mutation", "Hirschsprung disease and intellectual disability due to a ZEB2 point mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mowat-Wilson syndrome due to a ZEB2 point mutation", "shortest_name_length": 50}
{"curie": "UMLS:C4682659", "names": ["Stage IV Gestational Trophoblastic Neoplasm AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Gestational Trophoblastic Neoplasm AJCC v8", "shortest_name_length": 51}
{"curie": "MONDO:0008981", "names": ["infantile choroidocerebral calcification syndrome", "Infantile choroidocerebral calcification syndrome", "choroid plexus calcification and mental retardation", "Choroid Plexus Calcification and Mental Retardation", "CHOROID PLEXUS CALCIFICATION AND MENTAL RETARDATION", "Choroid plexus calcification and mental retardation", "Choroid plexus calcification with mental retardation", "choroid plexus calcification with mental retardation", "choroid plexus calcification and intellectual disability", "choroid plexus calcification with intellectual disability", "Choroido-cerebral calcification syndrome with retardation", "Infantile choroidocerebral calcification syndrome (disorder)", "infantile choroidocerebral calcification syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile choroidocerebral calcification syndrome", "shortest_name_length": 49}
{"curie": "UMLS:C0267440", "names": ["Toxic colitis", "toxic colitis", "toxic; colitis", "colitis; toxic", "toxic colitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "toxic colitis", "shortest_name_length": 13}
{"curie": "MONDO:0008611", "names": ["Humerus trochlea aplasia", "humerus trochlea aplasia", "Aplasia of trochlea of humerus", "aplasia of trochlea of the humerus", "trochlea of the humerus aplasia of", "TROCHLEA OF THE HUMERUS, APLASIA OF", "Trochlea of the Humerus, Aplasia of", "trochlea of the HUMERUS, aplasia OF", "Aplasia of trochlea of humerus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "humerus trochlea aplasia", "shortest_name_length": 24}
{"curie": "UMLS:C0855101", "names": ["Stage IV Small Lymphocytic Lymphoma", "stage IV small lymphocytic lymphoma", "Small Lymphocytic Lymphoma Stage IV", "small lymphocytic lymphoma, stage IV", "metastatic small lymphocytic lymphoma", "small lymphocytic lymphoma, metastatic", "B-cell small lymphocytic lymphoma stage IV", "Stage IV B-Cell Small Lymphocytic Lymphoma", "B-Cell Small Lymphocytic Lymphoma Stage IV", "Ann Arbor Stage IV Small Lymphocytic Lymphoma", "Small lymphocyte B lymphoma (Lukes-Collins Classification) stage IV"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-cell small lymphocytic lymphoma stage IV", "shortest_name_length": 35}
{"curie": "MONDO:0008684", "names": ["WHS", "PRDS", "monosomy 4p", "4p syndrome", "4p- syndrome", "4p- Syndrome", "Wolf syndrome", "PITT SYNDROME", "Pitt Syndrome", "wolf syndrome", "Pitt syndrome", "Wolf Syndrome", "syndromes wolf", "Syndrome, Pitt", "pitts syndrome", "syndrome wolfs", "Syndrome, Wolf", "Pitt Syndromes", "Syndromes, Pitt", "Del(4p) Syndrome", "del(4p) syndrome", "WITTWER SYNDROME", "Wittwer syndrome", "4P minus syndrome", "4p minus syndrome", "distal monosomy 4p", "Distal monosomy 4p", "Distal deletion 4p", "distal deletion 4p", "partial monosomy 4p", "Partial Monosomy 4p", "4p Deletion Syndrome", "4p deletion syndrome", "deletion 4p syndrome", "Telomeric deletion 4p", "telomeric deletion 4p", "Chromosome 4p Syndrome", "chromosome 4p syndrome", "chromosome 4p monosomy", "Chromosome 4p Monosomy", "Chromosome 4p Syndromes", "Syndrome, Chromosome 4p", "Wolf-Hirchhorn Syndrome", "4p Syndrome, Chromosome", "Wolf Hirchhorn Syndrome", "Wolf Hirschhorn Syndrome", "Wolff-Hirschorn syndrome", "wolff-Hirschorn syndrome", "WOLF-HIRSCHHORN SYNDROME", "Wolf-Hirschhorn syndrome", "Syndrome, Wolf-Hirchhorn", "4p Syndromes, Chromosome", "Wolf-Hirschhorn Syndrome", "Syndromes, Chromosome 4p", "Wolf Hirschhorn syndrome", "wolff-hirschorn syndrome", "wolf-hirschhorn syndrome", "Wolff-Hirschhorn syndrome", "Syndrome, Wolf-Hirschhorn", "PITT-ROGERS-DANKS SYNDROME", "Pitt Rogers Danks Syndrome", "pitt rogers danks syndrome", "Pitt-Rogers-Danks syndrome", "Pitt-Rogers-Danks Syndrome", "Syndrome, Pitt-Rogers-Danks", "4p partial monosomy syndrome", "Wolf-Hirschhorn syndrome (WHS)", "Midline fusion defect syndrome", "WHS - Wolff-Hirschorn syndrome", "chromosome 4p deletion syndrome", "Chromosome 4p Deletion Syndrome", "chromosome; 4 short arm deletion", "Pitt-Rogers-Danks syndrome (PRDS)", "deletion; short arm of chromosome 4", "Wolf Hirschhorn syndrome (disorder)", "chromosome 4P16.3 deletion syndrome", "CHROMOSOME 4p16.3 DELETION SYNDROME", "chromosome 4p16.3 deletion syndrome", "Wolf Hirschhorn syndrome (diagnosis)", "Deletion of short arm of chromosome 4", "deletion of short arm of chromosome 4", "4p partial monosomy syndrome (disorder)", "Chromosome 4 short arm deletion syndrome", "Wolf-Hirschhorn syndrome, Isolated cases", "syndrome; chromosome, 4 short arm deletion", "chromosome; syndrome, 4 short arm deletion", "deletion of short arm of chromosome 4 (diagnosis)", "anomaly of chromosome pair 4 Wolf Hirschhorn syndrome", "Chromosomal imbalance syndrome, pair 4, deletion, short arm", "Mental Retardation, Unusual Facies, And Intrauterine Growth Retardation", "unusual facies-mental retardation-intrauterine growth retardation syndrome", "microcephaly, IUGR, hypertelorism, ptosis, iris coloboma, hooked nose, external ear dysplasia, psychomotor retardation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wolf-Hirschhorn syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0019354", "names": ["Stickler syndrome", "stickler syndrome", "Stickler Syndrome", "sticklers syndrome", "Stickler dysplasia", "stickler's syndrome", "Stickler's syndrome", "arthro-ophthalmopathy", "Wagner-Stickler syndrome", "Stickler syndrome (disorder)", "Stickler syndrome (diagnosis)", "hereditary progressive arthroophthalmopathy", "Hereditary progressive arthroophthalmopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stickler syndrome", "shortest_name_length": 17}
{"curie": "MONDO:0016457", "names": ["ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome", "shortest_name_length": 76}
{"curie": "MONDO:0011686", "names": ["LIG4 syndrome", "LIG4 SYNDROME", "LIG4 Syndrome", "ligase 4 syndrome", "Ligase 4 syndrome", "DNA ligase IV deficiency", "LIG4 (ligase 4) syndrome", "Ligase 4 syndrome (disorder)", "Ligase 4 syndrome (diagnosis)", "Deoxyribonucleic acid ligase IV deficiency", "DNA (deoxyribonucleic acid) ligase IV deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DNA ligase IV deficiency", "shortest_name_length": 13}
{"curie": "UMLS:C1096185", "names": ["Dacryostenosis acquired"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dacryostenosis acquired", "shortest_name_length": 23}
{"curie": "MONDO:0004971", "names": ["Cylindroma", "cylindroma", "cylindromas", "Cylindromas", "cribriform carcinoma", "Adenocystic carcinoma", "adenocystic carcinoma", "Adenocystic Carcinoma", "adenoid cystic cancer", "Adenocystic Carcinomas", "Carcinoma, Adenocystic", "Carcinomas, Adenocystic", "adenoid cystic carcinoma", "Adenoid cystic carcinoma", "Adenoid Cystic Carcinoma", "carcinoma adenoid cystic", "adenoid cystic carcinomas", "Cylindroid adenocarcinoma", "Cylindroid Adenocarcinoma", "Cystic Carcinoma, Adenoid", "cylindroid adenocarcinoma", "Adenoid Cystic Carcinomas", "Carcinoma, Adenoid Cystic", "Cystic Carcinomas, Adenoid", "Adenocarcinoma, cylindroid", "Carcinomas, Adenoid Cystic", "Cylindroid bronchial adenoma", "Bronchial adenoma, cylindroid", "Adenocarcinoma, cylindroid type", "adenoid cystic carcinoma (diagnosis)", "Cylindroma (morphologic abnormality)", "Cylindroma (except Cylindroma of skin, M-82000)", "Adenoid cystic carcinoma (morphologic abnormality)", "Cylindroma, NOS (except Cylindroma of skin, M-82000)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenoid cystic carcinoma", "shortest_name_length": 10}
{"curie": "MONDO:0019726", "names": ["MC type II", "type II mixed cryoglobulinemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type II mixed cryoglobulinemia", "shortest_name_length": 10}
{"curie": "MONDO:0012002", "names": ["DFNB40", "autosomal recessive deafness 40", "Deafness, Autosomal Recessive 40", "deafness, autosomal recessive 40", "DEAFNESS, AUTOSOMAL RECESSIVE 40", "DEAFNESS, AUTOSOMAL RECESSIVE 40 (disorder)", "autosomal recessive nonsyndromic deafness 40", "autosomal recessive nonsyndromic hearing loss 40", "autosomal recessive nonsyndromic deafness type 40"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 40", "shortest_name_length": 6}
{"curie": "UMLS:C2983009", "names": ["Stage II Uterine Corpus Cancer", "Stage II Uterine Corpus Cancer AJCC v7", "Stage II Uterine (including Endometrial) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Uterine Corpus Cancer", "shortest_name_length": 30}
{"curie": "UMLS:C0600041", "names": ["Infection;bladder", "Infection bladder", "INFECTION BLADDER", "bladder infection", "BLADDER INFECTION", "Bladder infection", "bladder infections", "cystitis infective", "Bladder Infections", "bladder; infection", "infection; bladder", "Infective cystitis", "Infections, Bladder", "Infectious Cystitis", "infection of bladder", "Infection of bladder", "Bladder infection NOS", "Infective cystitis (disorder)", "Infective cystitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infective cystitis", "shortest_name_length": 17}
{"curie": "UMLS:C0346024", "names": ["Dermal Duct Tumor", "Dermal duct tumor", "Tumor, Dermal Duct", "Dermal duct tumour", "Duct Tumor, Dermal", "Dermal Duct Tumors", "Dermal Duct Neoplasm", "Eccrine dermal duct tumor", "Eccrine Dermal Duct Tumor", "Eccrine dermal duct tumour", "Eccrine Dermal Duct Neoplasm", "Eccrine dermal duct tumor of skin", "Eccrine dermal duct tumour of skin", "Dermal duct tumor (morphologic abnormality)", "Eccrine dermal duct tumor of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dermal Duct Tumor", "shortest_name_length": 17}
{"curie": "MONDO:0007453", "names": ["MODY2", "MODY type 2", "MODY, TYPE 2", "MODY, type 2", "MODY, Type 2", "MODY, type II", "MODY glucokinase-related", "MODY, glucokinase-related", "MODY, Glucokinase-Related", "MODY, GLUCOKINASE-RELATED", "diabetes mellitus MODY type 2", "GCK monogenic diabetes mellitus", "MODY 2 monogenic diabetes type 2", "GCK-associated diabetes mellitus", "GCK-Associated Diabetes Mellitus", "Maturity onset diabetes in youth type 2", "glucokinase-associated diabetes mellitus", "Maturity onset diabetes in youth type II", "Glucokinase-Associated Diabetes Mellitus", "maturity-onset diabetes of the young type 2", "diabetes mellitus autosomal dominant type 2", "type 2 diabetes mellitus autosomal dominant", "type 2 maturity-onset diabetes of the young", "Maturity-Onset Diabetes of the Young, Type 2", "Maturity onset diabetes of the young, type 2", "MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 2", "maturity onset diabetes of the Young, type 2", "maturity-onset diabetes of the young, type 2", "Diabetes mellitus autosomal dominant type II", "GCK (glucokinase) monogenic diabetes mellitus", "MODY - Maturity onset diabetes in youth type 2", "Diabetes Mellitus, Type II, Autosomal Dominant", "DIABETES MELLITUS, TYPE II, AUTOSOMAL DOMINANT", "MODY - Maturity onset diabetes in youth type II", "MODY - Maturity onset diabetes glucokinase-related", "GCK maturity-onset diabetes of the young (disease)", "Maturity onset diabetes of the young, type 2 (disorder)", "Diabetes mellitus autosomal dominant type II (disorder)", "diabetes mellitus autosomal dominant type 2 (diagnosis)", "maturity-onset diabetes of the young, type 2 (diagnosis)", "maturity-onset diabetes of the young (disease) caused by mutation in GCK"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maturity-onset diabetes of the young type 2", "shortest_name_length": 5}
{"curie": "UMLS:C0013221", "names": ["poison drug", "drugs poison", "Drug Toxicity", "Drug toxicity", "DRUG TOXICITY", "drug toxicity", "drugs poisons", "Toxicity, Drug", "toxicity, drug", "Drug poisoning", "drugs toxicity", "drug poisoning", "drugs poisoning", "drug toxicities", "Drug Toxicities", "drug; poisoning", "Poison;medicinal", "Toxicities, Drug", "DRUG INTOXICATION", "Drug toxicity NOS", "Drug intoxication", "drug intoxication", "medicinal toxicity", "Toxicity;medicinal", "drugs intoxication", "Medicinal poisoning", "MEDICATION TOXICITY", "DRUG TOXICITY (NOS)", "medicinal poisoning", "Drug toxicity (NOS)", "medication toxicity", "Drug poisoning, NOS", "Medicament poisoning", "Intoxication by drug", "SUBSTANCE INTOXICATION", "Therapeutic agent toxicity", "Overdose of drug with toxic effect", "drug/agent toxicity by tissue/organ", "Poisoning by drug or medicinal substance", "Poisoning by drug AND/OR medicinal substance", "Poisoning caused by drug or medicinal substance", "Poisoning caused by drug AND/OR medicinal substance", "Poisoning by unspecified drug or medicinal substance", "toxicity from drugs, medicaments, or biological substances", "Poisoning caused by drug AND/OR medicinal substance (disorder)", "toxicity from drugs, medicaments, or biological substances (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drug toxicity", "shortest_name_length": 11}
{"curie": "MONDO:0018234", "names": ["Dysostosis", "Dysostoses", "dysostosis", "Dysostosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dysostosis", "shortest_name_length": 10}
{"curie": "MONDO:0009313", "names": ["Grubben de Cock Borghgraef syndrome", "Grubben-de Cock-Borghgraef syndrome", "Grubben, De Cock, Borghgraef syndrome", "Grubben, De Cock, Borghgraef syndrome (disorder)", "Grubben, De Cock, Borghgraef syndrome (diagnosis)", "developmental delay - hypotonia - extremities hypertrophy", "Developmental delay-hypotonia-extremities hypertrophy syndrome", "GROWTH RETARDATION, SMALL AND PUFFY HANDS AND FEET, AND ECZEMA", "developmental delay-hypotonia-extremities hypertrophy syndrome", "growth retardation, small and puffy hands and feet, and eczema", "Growth Retardation, Small and Puffy Hands and Feet, and Eczema", "Developmental delay, hypotonia, extremities hypertrophy syndrome", "severe growth retardation, developmental delay with hypotonia, hypotrophy of the distal extremities, dental anomalies, and eczematous skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grubben-de Cock-Borghgraef syndrome", "shortest_name_length": 35}
{"curie": "MONDO:0018566", "names": ["short stature-advanced bone age-early-onset osteoarthritis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short stature-advanced bone age-early-onset osteoarthritis syndrome", "shortest_name_length": 67}
{"curie": "MONDO:0002435", "names": ["Oculomotor Nerve Tumor", "Oculomotor nerve tumor", "oculomotor nerve tumor", "cranial nerve III tumor", "Oculomotor nerve tumour", "Cranial Nerve III Tumor", "cranial nerve III tumour", "IIIrd Cranial Nerve Tumor", "oculomotor nerve neoplasm", "tumor of oculomotor nerve", "Oculomotor Nerve Neoplasm", "IIIrd cranial nerve tumor", "neoplasm of oculomotor nerve", "Neoplasm of oculomotor nerve", "neoplasm of third cranial nerve", "oculomotor nerve neoplasm (disease)", "Neoplasm of oculomotor nerve (disorder)", "neoplasm of third cranial nerve (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculomotor nerve neoplasm", "shortest_name_length": 22}
{"curie": "MONDO:0010526", "names": ["Fd", "FD", "Fabry", "fabri disease", "Fabry Disease", "FABRY DISEASE", "disease fabry", "fabry disease", "Fabry disease", "Anderson-Fabry", "Fabry syndrome", "GLA deficiency", "GLA DEFICIENCY", "Gla deficiency", "fabrys disease", "GLA Deficiency", "Deficiency, GLA", "disease fabry's", "Fabry's disease", "Fabry's Disease", "fabry's disease", "FABRY'S DISEASE", "Lactosyl ceramidosis", "Diffuse Angiokeratoma", "Diffuse angiokeratoma", "diffuse angiokeratoma", "Angiokeratoma Diffuse", "ANDERSON-FABRY DISEASE", "anderson-fabry disease", "Anderson-Fabry disease", "Anderson Fabry Disease", "Angiokeratoma, Diffuse", "Anderson-Fabry Disease", "Ruiter-Pompen syndrome", "angiokeratoma, diffuse", "Deficiency of melibiase", "deficiency of melibiase", "ceramide trihexosidosis", "Cardiovasorenal syndrome", "Sweeley-Klionsky disease", "Thesaurismosis lipoidica", "Fabry (-Anderson) disease", "Fabry's disease (disorder)", "Thesaurismosis hereditaria", "thesaurismosis hereditaria", "Fabry's disease (diagnosis)", "Ceramide lactoside lipidosis", "hereditary dystopic lipidosis", "Hereditary Dystopic Lipidosis", "HEREDITARY DYSTOPIC LIPIDOSIS", "Hereditary dystopic lipidosis", "Fabry disease, Cardiac variant", "Fabry Disease, Cardiac Variant", "FABRY DISEASE, CARDIAC VARIANT", "Lipidosis, Hereditary Dystopic", "alpha galactosidase deficiency", "Angiokeratoma Corporis Diffusum", "Angiokeratoma corporis diffusum", "angiokeratoma corporis diffusum", "ANGIOKERATOMA CORPORIS DIFFUSUM", "alpha-Galactosidase-A deficiency", "angiokeratoma; corporis diffusum", "Alpha galactosidase A deficiency", "alpha-Galactosidase A Deficiency", "alpha Galactosidase A Deficiency", "Alpha-galactosidase A deficiency", "Trihexosidase deficiency disease", "ALPHA-GALACTOSIDASE A DEFICIENCY", "Alpha-Galactosidase A Deficiency", "corporis diffusum; angiokeratoma", "CERAMIDE TRIHEXOSIDASE DEFICIENCY", "Ceramide Trihexosidase Deficiency", "Deficiency of alpha-galactosidase", "Ceramide trihexosidase deficiency", "ceramide trihexosidase deficiency", "Deficiency, alpha-Galactosidase A", "Deficiency, Ceramide Trihexosidase", "alpha-Galactosidase A Deficiency Disease", "alpha Galactosidase A Deficiency Disease", "Angiokeratoma corporis diffusum universale", "Deficiency of alpha-galactosidase (disorder)", "Deficiency of alpha-galactosidase (diagnosis)", "CERAMIDE TRIHEXOSIDE LIPOIDOSIS FABRYS DISEASE", "CERAMIDE TRIHEXOSIDE LIPOIDOSIS <FABRYS DISEASE>"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fabry disease", "shortest_name_length": 2}
{"curie": "MONDO:0015128", "names": ["primary adrenal insufficiency", "Primary adrenal insufficiency", "Primary Adrenal Insufficiency", "Primary adrenocortical failure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary adrenal insufficiency", "shortest_name_length": 29}
{"curie": "MONDO:0017381", "names": ["neonatal HSV infection", "neonatal herpes simplex", "herpes simplex neonatal", "Neonatal herpes simplex", "congenital HSV infection", "congenital herpes simplex", "Congenital herpes simplex", "herpes; simplex, congenital", "congenital; herpes (simplex)", "congenital herpes simplex infection", "congenital Herpes simplex infection", "Congenital herpes simplex infection", "Congenital herpes simplex (disorder)", "infection; congenital, herpes simplex", "neonatal herpes simplex virus infection", "Simplexvirus infectious embryofetopathy", "antenatal herpes simplex virus infection", "congenital herpes simplex virus infection", "Simplexvirus caused infectious embryofetopathy", "congenital Herpes simplex infection (diagnosis)", "mother-to-child transmission of herpes simplex virus infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital herpes simplex virus infection", "shortest_name_length": 22}
{"curie": "UMLS:C0269842", "names": ["Uterine hypertonus", "Uterine polysystole", "Uterine tachysystole", "Uterine hyperstimulation", "uterine hyperstimulation", "Hypertonic uterine activity", "Hypertonic uterine dysfunction", "hypertonic uterine dysfunction", "Hypertonic uterine contraction", "uterus; contraction, hypertonic", "hypertonic uterine contractions", "Uterine contraction, hypertonic", "contraction; uterus, hypertonic", "contractions hypertonic uterine", "Hypertonic uterine dysfunction (disorder)", "hypertonic uterine contractions (diagnosis)", "uterine inertia abnormality of forces of labor hypertonic uterine dysfunction", "uterine inertia abnormality of forces of labor hypertonic uterine dysfunction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypertonic uterine dysfunction", "shortest_name_length": 18}
{"curie": "MONDO:0007417", "names": ["DD", "dar", "DAR", "DARIER DISEASE", "Darier disease", "darier disease", "Psorospermosis", "Darier Disease", "Disease, Darier", "dariers disease", "Dariers Disease", "darier's disease", "Darier's Disease", "Darier's disease", "DARIER'S DISEASE", "Disease, Darier's", "WHITE-DARIER DISEASE", "Darier-White Disease", "Follicular keratosis", "darier white disease", "Darier White disease", "Darier White Disease", "Darier-White disease", "DARIER-WHITE DISEASE", "follicular keratosis", "darier-white disease", "Keratosis follicular", "Disease, Darier-White", "Darier-White Diseases", "Keratosis follicularis", "Diseases, Darier-White", "KERATOSIS FOLLICULARIS", "Keratosis Follicularis", "keratitis follicularis", "keratosis follicularis", "follicularis; keratosis", "keratosis; follicularis", "DARIER DISEASE, SEGMENTAL", "Dyskeratosis follicularis", "Darier disease (disorder)", "Darier disease, segmental", "Darier Disease, Segmental", "PSOROSPERMOSIS, FOLLICULARIS", "Hereditary follicular keratosis", "keratitis follicularis (diagnosis)", "Psorospermosis follicularis vegetans", "DARIER DISEASE, ACRAL HEMORRHAGIC TYPE", "Darier Disease, Acral Hemorrhagic Type", "Darier disease, acral hemorrhagic type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Darier disease", "shortest_name_length": 2}
{"curie": "MONDO:0022968", "names": ["situs inversus totalis", "dextrocardia with situs inversus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dextrocardia with situs inversus", "shortest_name_length": 22}
{"curie": "MONDO:0022985", "names": ["cavernous haemangioma of the rectum", "diffuse cavernous hemangioma of the rectum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diffuse cavernous hemangioma of the rectum", "shortest_name_length": 35}
{"curie": "MONDO:0015692", "names": ["RAEB-T", "RAEB-t", "refractory anemia with excess blasts in transformation", "Refractory anemia with excess blasts in transformation", "Refractory Anemia with Excess Blasts in Transformation", "Refractory anaemia with excess blasts in transformation", "Refractory anemia with excess of blasts with transformation", "Refractory anaemia with excess of blasts with transformation", "Refractory anemia with excess blasts in transformation [RAEB T]", "RAEB-T - Refractory anemia with excess blasts in transformation", "RAEB-T - Refractory anaemia with excess blasts in transformation", "Refractory anemia with excess blasts in transformation (disorder)", "Refractory anemia with excess blasts in transformation (clinical)", "Refractory anaemia with excess blasts in transformation (clinical)", "Refractory anemia with excess blasts in transformation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "refractory anemia with excess blasts in transformation", "shortest_name_length": 6}
{"curie": "MONDO:0001536", "names": ["vagina leiomyoma", "Vaginal Leiomyoma", "vaginal leiomyoma", "leiomyoma of vagina", "Leiomyoma of Vagina", "leiomyoma of the vagina", "Leiomyoma of the Vagina"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vaginal leiomyoma", "shortest_name_length": 16}
{"curie": "UMLS:C4682586", "names": ["Stage IIIC Uterine Corpus Adenosarcoma", "Stage IIIC Uterine Corpus Adenosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Uterine Corpus Adenosarcoma AJCC v8", "shortest_name_length": 38}
{"curie": "MONDO:0024659", "names": ["Colorectal Kaposi Sarcoma", "colorectal Kaposi sarcoma", "large intestinal Kaposi sarcoma", "Large Intestinal Kaposi Sarcoma", "large intestine Kaposi's sarcoma (disease)", "Kaposi's sarcoma (disease) of large intestine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorectal Kaposi sarcoma", "shortest_name_length": 25}
{"curie": "MONDO:0010260", "names": ["ACLLX", "AMCX5, FORMERLY", "Arthrogryposis, X-Linked, Type V", "arthrogryposis, X-linked, type V", "ARTHROGRYPOSIS, X-LINKED, TYPE V, FORMERLY", "arthrogryposis, X-linked, type V, formerly", "arthrogryposis, congenital, lower limb, X-linked", "arthrogryposis, congenital, LOWER limb, X-linked", "ARTHROGRYPOSIS, CONGENITAL, LOWER LIMB, X-LINKED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis, congenital, lower limb, X-linked", "shortest_name_length": 5}
{"curie": "UMLS:C0280097", "names": ["squamous cell CUP", "CUP, squamous cell", "unknown primary, squamous cell carcinoma", "squamous cell carcinoma, unknown primary", "squamous cell carcinoma of unknown primary", "Squamous Cell Carcinoma of Unknown Primary", "Squamous Cell Cancer of Unknown Primary Origin", "Squamous Cell Carcinoma of Occult Primary Site", "Epidermoid Carcinoma of Unknown Primary Origin", "Squamous Cell Carcinoma of Unknown Primary Origin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Squamous Cell Carcinoma of Unknown Primary", "shortest_name_length": 17}
{"curie": "MONDO:0004045", "names": ["Intraocular Retinoblastoma", "intraocular retinoblastoma", "retinoblastoma, intraocular", "Childhood Intraocular Retinoblastoma", "childhood intraocular retinoblastoma", "Pediatric Intraocular Retinoblastoma", "pediatric intraocular retinoblastoma", "intraocular retinoblastoma of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pediatric intraocular retinoblastoma", "shortest_name_length": 26}
{"curie": "UMLS:C1333041", "names": ["CLL with Unmutated IGVH", "Pregerminal Center Chronic Lymphocytic Leukemia", "Chronic Lymphocytic Leukemia with Unmutated Immunoglobulin Heavy Chain Variable-Region Gene"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic Lymphocytic Leukemia with Unmutated Immunoglobulin Heavy Chain Variable-Region Gene", "shortest_name_length": 23}
{"curie": "MONDO:0004026", "names": ["Tag", "Tag, NOS", "Skin tag", "skin tag", "SKIN TAG", "Skin Tag", "tag; skin", "skin tags", "Skin tags", "SKIN POLYP", "Acrochorda", "SKIN TAG S", "skin polyp", "Acrochordon", "SKIN TAG(S)", "skin polyps", "acrochordon", "Soft fibroma", "Soft Fibroma", "Achrochordon", "achrochordon", "soft fibroma", "acrochordons", "cutaneous tag", "Fibroma Molle", "Fibrous polyp", "Cutaneous Tag", "Fibrous Polyp", "Fibroma molle", "fibroma molle", "Polyp(s);skin", "Cutaneous tag", "cutaneous tags", "SKT - Skin tag", "Soft papilloma", "Cutaneous polyp", "Skin tag (disorder)", "fibroepithelial polyp", "Fibroepithelial polyp", "Fibroepithelial Polyp", "POLYP FIBROEPITHELIAL", "Polyp, fibroepithelial", "fibroepithelial polyps", "Acrochordons (skin tag)", "acrochordon (diagnosis)", "Fibroepithelial papilloma", "skin tag (physical finding)", "fibroepithelial polyp of skin", "Fibroepithelial polyp of skin", "Tag (morphologic abnormality)", "Fibroepithelial Polyp of Skin", "cutaneous fibroepithelial polyp", "Cutaneous Fibroepithelial Polyp", "Fibroepithelial Polyp of the Skin", "fibroepithelial polyp of the skin", "Fibroepithelial polyp (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin tag", "shortest_name_length": 3}
{"curie": "MONDO:0007618", "names": ["Eng-Strom syndrome", "Short stature and locking fingers", "short stature-locking fingers syndrome", "finger locking, recurrent, with intrauterine growth retardation and proportionate short stature", "FINGER LOCKING, RECURRENT, WITH INTRAUTERINE GROWTH RETARDATION AND PROPORTIONATE SHORT STATURE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eng-Strom syndrome", "shortest_name_length": 18}
{"curie": "UMLS:C3495145", "names": ["dyslalia", "Dyslalia", "Dyslalias", "dyslalias", "Dyslalia (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dyslalia", "shortest_name_length": 8}
{"curie": "MONDO:0021110", "names": ["Acrospiroma", "hidradenoma", "Hidradenoma", "syringadenoma", "Syringadenoma", "Syringadenomas", "Acrospiradenoma", "Hidradenoma, NOS", "Syringadenoma, NOS", "Sweat Gland Adenoma", "Eccrine Acrospiroma", "Hidradenoma of skin", "Sweat gland adenoma", "sweat gland adenoma", "Adenoma, Sweat Gland", "Sweat Gland Adenomas", "Adenomas, Sweat Gland", "Hidradenoma morphology", "adenoma of sweat gland", "Adenoma of Sweat Gland", "[M]Sweat gland adenoma", "adenoma of the sweat gland", "Adenoma of the Sweat Gland", "adenoma, sweat gland, benign", "ADENOMA, SWEAT GLAND, BENIGN", "Hidradenoma of skin (disorder)", "Sweat gland adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sweat gland adenoma", "shortest_name_length": 11}
{"curie": "MONDO:0007682", "names": ["Granddad Syndrome", "granddad syndrome", "GRANDDAD SYNDROME", "Growth retardation, aged facies, normal development, decreased subcutaneous fat, autosomal dominant inheritance", "GROWTH RETARDATION, AGED FACIES, NORMAL DEVELOPMENT, DECREASED SUBCUTANEOUS FAT, AUTOSOMAL DOMINANT INHERITANCE", "Growth Retardation, Aged Facies, Normal Development, Decreased Subcutaneous Fat, Autosomal Dominant Inheritance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "granddad syndrome", "shortest_name_length": 17}
{"curie": "UMLS:C0279625", "names": ["Adult APL", "adult APL", "APL, adult", "M3 Adult Acute Leukemia", "Adult Acute M3 Leukemia", "adult acute M3 leukemia", "M3 leukemia, adult acute", "Adult Acute Promyelocytic Leukemia", "leukemia, adult acute promyelocytic", "acute promyelocytic leukemia, adult", "promyelocytic leukemia, adult acute", "adult acute progranulocytic leukemia", "M3 Adult Acute Promyelocytic Leukemia", "progranulocytic leukemia, adult acute", "M3 adult acute promyelocytic leukemia", "acute progranulocytic leukemia, adult", "Adult Acute Promyelocytic Leukemia (M3)", "adult acute promyelocytic leukemia (M3)", "Acute Promyelocytic Leukemia with PML-RARA", "Adult Acute Promyelocytic Leukemia with PML-RARA", "adult acute myeloid leukemia with t(15;17)(q22;q12)", "adult acute myeloid leukemia with PML/RARalpha translocation", "Adult Acute Promyelocytic Leukemia with t(15;17)(q22;q12)(PML/RARa)", "Adult Acute Promyelocytic Leukemia with t(15;17)(q22;q12); PML-RARA", "Adult Acute Promyelocytic Leukemia with t(15;17)(q22;q12); PML/RARA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Acute Promyelocytic Leukemia with PML-RARA", "shortest_name_length": 9}
{"curie": "MONDO:0044633", "names": ["IPPFE", "idiopathic pleuropulmonary fibroelastosis", "idiopathic pleuroparenchymal fibroelastosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic pleuroparenchymal fibroelastosis", "shortest_name_length": 5}
{"curie": "MONDO:0023609", "names": ["Le Marec Bracq Picaud syndrome", "le Marec-Bracq-Picaud syndrome", "Complex malformation syndrome with brachymesomelia", "complex malformation syndrome with brachymesomelia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "le Marec-Bracq-Picaud syndrome", "shortest_name_length": 30}
{"curie": "MONDO:0011180", "names": ["BROAD TERMINAL PHALANGES, FAMILIAL", "Broad Terminal Phalanges, Familial", "broad terminal phalanges, familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "broad terminal phalanges, familial", "shortest_name_length": 34}
{"curie": "MONDO:0000858", "names": ["intestinal pseudo-obstruction", "Intestinal neuronal dysplasia", "intestinal neuronal dysplasia", "Neuronal intestinal dysplasia", "neuronal intestinal dysplasia", "Chronic intestinal pseudo-obstruction", "Neuronal intestinal dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuronal intestinal dysplasia", "shortest_name_length": 29}
{"curie": "MONDO:0010969", "names": ["CORD5", "cone-rod dystrophy 5", "Cone-Rod Dystrophy 5", "CONE-ROD DYSTROPHY 5", "cone-rod dystrophy type 5", "PITPNM3 cone-rod dystrophy", "cone-rod dystrophy caused by mutation in PITPNM3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cone-rod dystrophy 5", "shortest_name_length": 5}
{"curie": "UMLS:C3496580", "names": ["Inferior Vena Cava Occlusion", "Inferior vena caval occlusion", "Occlusion of inferior vena cava", "Inferior caval vein obstruction", "Obstruction of inferior vena cava", "Occlusion of inferior vena cava (disorder)", "Obstruction of inferior vena cava (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Occlusion of inferior vena cava", "shortest_name_length": 28}
{"curie": "MONDO:0030397", "names": ["NCPH2", "PORTAL HYPERTENSION, NONCIRRHOTIC, 2", "portal hypertension, noncirrhotic, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "portal hypertension, noncirrhotic, 2", "shortest_name_length": 5}
{"curie": "MONDO:0011254", "names": ["brachydactyly, intraventricular septal defect, and deafness", "BRACHYDACTYLY, INTRAVENTRICULAR SEPTAL DEFECT, AND DEAFNESS", "Brachydactyly, Intraventricular Septal Defect, And Deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly, intraventricular septal defect, and deafness", "shortest_name_length": 59}
{"curie": "UMLS:C4724503", "names": ["Recurrent Myelodysplastic Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Myelodysplastic Syndrome", "shortest_name_length": 34}
{"curie": "MONDO:0014603", "names": ["DFNA40", "autosomal dominant deafness 40", "DEAFNESS, AUTOSOMAL DOMINANT 40", "deafness, autosomal dominant 40", "deafness, autosomal dominant type 40", "autosomal dominant nonsyndromic deafness 40", "CRYM autosomal dominant nonsyndromic deafness", "autosomal dominant nonsyndromic hearing loss 40", "autosomal dominant nonsyndromic deafness type 40", "autosomal dominant nonsyndromic deafness caused by mutation in CRYM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 40", "shortest_name_length": 6}
{"curie": "UMLS:C0434159", "names": ["fracture penis", "penis fracture", "Penile fracture", "penile fracture", "fractures penile", "fracture of penis", "Fracture of penis", "Fracture of erect penis", "Fracture of erect penis (disorder)", "Rupture of corpus cavernosum of penis", "Rupture of corpus cavernosum of penis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fracture of erect penis", "shortest_name_length": 14}
{"curie": "MONDO:0004366", "names": ["Mixed Astrocytoma-Ependymoma-Oligodendroglioma", "mixed astrocytoma-ependymoma-oligodendroglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed astrocytoma-ependymoma-oligodendroglioma", "shortest_name_length": 46}
{"curie": "UMLS:C0855094", "names": ["Stage IV B Cell Lymphoma", "Stage IV B-Cell Lymphoma", "B Cell Lymphoma Stage IV", "B-cell lymphoma stage IV", "B-Cell Lymphoma Stage IV", "Stage IV B-Cell Non-Hodgkin Lymphoma", "Stage IV B-Cell Non-Hodgkin's Lymphoma", "Ann Arbor Stage IV B-Cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-cell lymphoma stage IV", "shortest_name_length": 24}
{"curie": "MONDO:0011240", "names": ["MCM", "M-CM", "MCAP", "MCMTC", "M-CMTC", "Macrocephaly-capillary malformation", "Macrocephaly-Capillary Malformation", "macrocephaly-capillary malformation", "MACROCEPHALY-CAPILLARY MALFORMATION", "Megalencephaly capillary malformation", "M-CM (Macrocephaly-capillary malformation)", "Macrocephaly-capillary malformation syndrome", "MCAP - megalencephaly capillary malformation", "macrocephaly-capillary malformation syndrome", "megalencephaly-capillary malformation syndrome", "MEGALENCEPHALY-CAPILLARY MALFORMATION SYNDROME", "Megalencephaly-capillary malformation syndrome", "Megalencephaly capillary malformation (disorder)", "Macrocephaly-cutis marmorata telangiectatica congenita", "MACROCEPHALY-CUTIS MARMORATA TELANGIECTATICA CONGENITA", "Macrocephaly cutis marmorata telangiectatica congenita", "Macrocephaly-Cutis Marmorata Telangiectatica Congenita", "macrocephaly cutis marmorata telangiectatica congenita", "macrocephaly-cutis marmorata telangiectatica congenita", "megalocephaly cutis marmorata telangiectatica congenita", "Megalocephaly cutis marmorata telangiectatica congenita", "Megalencephaly-Cutis Marmorata Telangiectatica Congenita", "MEGALENCEPHALY-CUTIS MARMORATA TELANGIECTATICA CONGENITA", "megalencephaly cutis marmorata telangiectatica congenita", "megalencephaly-cutis marmorata telangiectatica congenita", "Megalencephaly cutis marmorata telangiectatica congenita", "MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME", "megalencephaly-capillary malformation-polymicrogyria syndrome", "Megalencephaly-capillary malformation-polymicrogyria syndrome", "Macrocephaly-cutis marmorata telangiectatica congenita syndrome", "Megalencephaly, capillary malformation, polymicrogyria syndrome", "macrocephaly-cutis marmorata telangiectatica congenita syndrome", "Megalencephaly-cutis marmorata telangiectatica congenita syndrome", "megalencephaly-cutis marmorata telangiectatica congenita syndrome", "megalencephaly-capillary malformation-polymicrogyria syndrome, somatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "megalencephaly-capillary malformation-polymicrogyria syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C2825055", "names": ["Recurrence", "recurrence", "RECURRENCE", "recurrences", "Recurrences", "relapse/recurrence", "Recurrence (disease attribute)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrence (disease attribute)", "shortest_name_length": 10}
{"curie": "MONDO:0018301", "names": ["IC", "PBS", "IC/PBS", "IC/BPS", "Ulcerative cystitis", "ulcerative cystitis", "Cystitis ulcerative", "cystitis ulcerative", "CYSTITIS ULCERATIVE", "CYSTITIS INTERSTITIAL", "bladder pain syndrome", "Interstitial cystitis", "Bladder Pain Syndrome", "Interstitial Cystitis", "INTERSTITIAL CYSTITIS", "interstitial cystitis", "Cystitis;interstitial", "Bladder pain syndrome", "Cystitis interstitial", "Pain Syndrome, Bladder", "interstitial; cystitis", "cystitis; interstitial", "Cystitis, Interstitial", "Bladder Pain Syndromes", "Interstitial Cystitides", "Painful bladder syndrome", "Cystitides, Interstitial", "painful bladder syndrome", "Painful Bladder Syndrome", "interstitial cystitis (IC)", "IC - Interstitial cystitis", "chronic interstitial cystitis", "Chronic interstitial cystitis", "Chronic Interstitial Cystitis", "Cystitis, Chronic Interstitial", "Interstitial Cystitis, Chronic", "Ulcerative cystitis (disorder)", "painful bladder syndrome (PBS)", "interstitial cystitis, chronic", "PBS - Painful bladder syndrome", "CYSTITIS, CHRONIC INTERSTITIAL", "Chronic Interstitial Cystitides", "cystitis; chronic, interstitial", "chronic; cystitis, interstitial", "Interstitial cystitis (chronic)", "Ulcerative cystitis (diagnosis)", "Interstitial Cystitides, Chronic", "Cystitides, Chronic Interstitial", "Chronic interstitial cystitis NOS", "Chronic interstitial cystitis (disorder)", "chronic interstitial cystitis (diagnosis)", "interstitial cystitis/bladder pain syndrome", "Interstitial cystitis/bladder pain syndrome", "interstitial cystitis/painful bladder syndrome", "Interstitial cystitis/painful bladder syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "interstitial cystitis", "shortest_name_length": 2}
{"curie": "MONDO:0009861", "names": ["PKU", "PHENYLKETOURIA", "PAH deficiency", "phenylketouria", "PHENYLKETONURIA", "phenylketonuria", "Folling disease", "Phenylketonuria", "phenylketonurias", "Phenylketonurias", "Phenylalaninemia", "phenylalaninemia", "Folling's disease", "HPA, NON-PKU MILD", "HPA, non-PKU mild", "Phenylalaninaemia", "pku phenylketonuria", "Phenylketonuria, NOS", "phenylketonuria (PKU)", "PKU - phenylketonuria", "Phenylketonuria [PKU]", "PKU - Phenylketonuria", "Phenylketonuria (PKU)", "maternal phenylketonuria", "phenylketonuria, maternal", "PKU (Hereditary Disorder)", "imbecilitus phenylpyruvica", "Phenylketonuria (disorder)", "phenylpyruvic oligophrenia", "Oligophrenia phenylpyruvica", "oligophrenia phenylpyruvica", "oligophrenia Phenylpyruvica", "phenylketonuria (diagnosis)", "HYPERPHENYLALANINEMIA, NON-PKU MILD", "hyperphenylalaninemia, non-PKU mild", "Hyperphenylalaninemia, Non-Pku Mild", "phenylalanine hydroxylase deficiency", "Phenylalanine hydroxylase deficiency", "PAH (phenylalanine hydroxylase) deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phenylketonuria", "shortest_name_length": 3}
{"curie": "MONDO:0010896", "names": ["PDS", "OPDG", "GPDS1", "Pigment dispersion syndrome", "pigment dispersion syndrome", "Pigment-Dispersion Syndrome", "pigment-dispersion syndrome", "PIGMENT DISPERSION SYNDROME", "Pigment Dispersion Syndrome", "pigment-dispersion type glaucoma", "GLAUCOMA, PIGMENT-DISPERSION TYPE", "Glaucoma, Pigment-Dispersion Type", "glaucoma, pigment-dispersion type", "Pigment dispersion syndrome (disorder)", "GLAUCOMA-RELATED PIGMENT DISPERSION SYNDROME", "glaucoma-related pigment dispersion syndrome", "Glaucoma-Related Pigment Dispersion Syndrome", "glaucoma-RELATED pigment dispersion syndrome", "OCULAR PIGMENT DISPERSION WITH OR WITHOUT GLAUCOMA", "GPDS1 Glaucoma-Related Pigment Dispersion Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pigment dispersion syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0004881", "names": ["Myositis fibrosa", "myositis fibrosa", "interstitial myositis", "Interstitial Myositis", "Interstitial myositis", "interstitial; myositis", "myositis; interstitial", "Interstitial myositis (disorder)", "interstitial myositis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myositis fibrosa", "shortest_name_length": 16}
{"curie": "UMLS:C0280387", "names": ["nasopharynx lymphoepithelioma, recurrent", "Relapsed Lymphoepithelioma of Nasopharynx", "Nasopharyngeal lymphepithelioma recurrent", "Relapsed Nasopharyngeal Lymphoepithelioma", "Nasopharyngeal lymphoepithelioma recurrent", "Recurrent Nasopharyngeal Lymphoepithelioma", "Recurrent Lymphoepithelioma of Nasopharynx", "nasopharyngeal lymphoepithelioma, recurrent", "Relapsed Lymphoepithelioma of the Nasopharynx", "recurrent lymphoepithelioma of the nasopharynx", "Recurrent Lymphoepithelioma of the Nasopharynx", "lymphoepithelioma of the nasopharynx, recurrent", "Relapsed Nasopharyngeal Undifferentiated Carcinoma", "Relapsed Undifferentiated Carcinoma of Nasopharynx", "Recurrent Undifferentiated Carcinoma of Nasopharynx", "Recurrent Nasopharyngeal Undifferentiated Carcinoma", "Relapsed Undifferentiated Carcinoma of the Nasopharynx", "Recurrent Undifferentiated Carcinoma of the Nasopharynx", "Recurrent Nasopharyngeal Throat Undifferentiated Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasopharyngeal lymphoepithelioma recurrent", "shortest_name_length": 40}
{"curie": "MONDO:0018169", "names": ["Ectasic coloboma", "Volubilis syndrome", "morning glory syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "morning glory syndrome", "shortest_name_length": 16}
{"curie": "UMLS:C0855004", "names": ["Lung carcinoma stage III", "Carcinoma of lung stage III", "Pulmonary carcinoma stage III", "Lung carcinoma cell type unspecified stage III", "Stage III Lung Carcinoma Cell Type Unspecified", "Carcinoma of lung cell type unspecified stage III", "Pulmonary carcinoma cell type unspecified stage III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Lung Carcinoma Cell Type Unspecified", "shortest_name_length": 24}
{"curie": "UMLS:C4528552", "names": ["Stage IA Breast Cancer", "Anatomic Stage IA Breast Cancer AJCC v8", "Anatomic Stage IA Breast Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anatomic Stage IA Breast Cancer AJCC v8", "shortest_name_length": 22}
{"curie": "UMLS:C5670413", "names": ["Unresectable Primary Peritoneal High-Grade Serous Adenocarcinoma", "Unresectable Primary Peritoneal High Grade Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Primary Peritoneal High Grade Serous Adenocarcinoma", "shortest_name_length": 64}
{"curie": "UMLS:C0233558", "names": ["tantrum", "Tantrums", "tantrums", "temper tantrum", "Temper tantrum", "temper, tantrum", "temper tantrums", "tantrums temper", "Temper Tantrums", "Temper tantrums", "Temper tantrum (finding)", "temper, tantrum; conduct disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Temper tantrum", "shortest_name_length": 7}
{"curie": "EFO:0010098", "names": ["stress-related disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stress-related disorder", "shortest_name_length": 23}
{"curie": "MONDO:0034971", "names": ["isolated congenital entropion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated congenital entropion", "shortest_name_length": 29}
{"curie": "UMLS:C5556682", "names": ["Locally Advanced Desmoplastic Small Round Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Desmoplastic Small Round Cell Tumor", "shortest_name_length": 52}
{"curie": "UMLS:C0001539", "names": ["ADJUSTMENT DISORDER WITH DEPRESSED MOOD", "adjustment disorder with depressed mood", "Adjustment disorder with depressed mood", "Adjustment disorders, With depressed mood", "Adjustment disorder with depressed mood (disorder)", "adjustment disorder with depressed mood (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adjustment disorder with depressed mood", "shortest_name_length": 39}
{"curie": "UMLS:C0852066", "names": ["Congenital thyroid disorder", "Congenital Thyroid Disorder", "Thyroid disorders congenital", "Congenital Thyroid Gland Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital thyroid disorder", "shortest_name_length": 27}
{"curie": "UMLS:C4528558", "names": ["Stage IIIA Breast Cancer", "Anatomic Stage IIIA Breast Cancer AJCC v8", "Anatomic Stage IIIA Breast Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anatomic Stage IIIA Breast Cancer AJCC v8", "shortest_name_length": 24}
{"curie": "UMLS:C4553844", "names": ["Stage IV Thyroid Gland Follicular Cancer", "Stage IV Thyroid Gland Follicular Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Thyroid Gland Follicular Carcinoma AJCC v8", "shortest_name_length": 40}
{"curie": "MONDO:0015376", "names": ["First branchial cleft cyst", "first branchial cleft cyst", "Type 1 branchial cleft cyst", "first branchial cleft fistula", "first branchial cleft anomaly", "First branchial cleft fistula", "First branchial cleft anomaly", "First branchial cleft cyst (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "first branchial cleft anomaly", "shortest_name_length": 26}
{"curie": "UMLS:C0744049", "names": ["Flank Mass", "FLANK MASS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Flank Mass", "shortest_name_length": 10}
{"curie": "MONDO:0003937", "names": ["spondylitis", "Spondylitis", "SPONDYLITIS", "Spondylitides", "Spondylitis NOS", "Spondylitis, NOS", "vertebra inflammation", "Spondylitis (disorder)", "spondylitis (diagnosis)", "inflammation of vertebra", "inflammatory spondylopathy", "spondylopathy inflammatory", "inflammatory; spondylopathy", "spondylopathy; inflammatory", "inflammation of the vertebra", "Undifferentiated spondylitis", "Inflammatory spondylopathy, NOS", "Other inflammatory spondylopathies", "spondylopathy inflammatory (diagnosis)", "Unspecified inflammatory spondylopathy", "Inflammatory spondylopathy, unspecified", "Undifferentiated spondylitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondylitis", "shortest_name_length": 11}
{"curie": "MONDO:0008725", "names": ["CLAH", "LCAH", "Adrenal Hyperplasia I", "ADRENAL HYPERPLASIA I", "Adrenal hyperplasia 1", "adrenal hyperplasia 1", "20,22-Desmolase deficiency", "lipoid adrenal hyperplasia", "20,22-desmolase deficiency", "Cholesterol desmolase deficiency", "lipoid congenital adrenal hyperplasia", "LIPOID CONGENITAL ADRENAL HYPERPLASIA", "Congenital Lipoid Adrenal Hyperplasia", "Lipoid congenital adrenal hyperplasia", "congenital adrenal hyperplasia lipoid", "20,22-desmolase deficiency (diagnosis)", "Defective synthesis of cholesterol desmolase", "Cholesterol monooxygenase (side-chain cleaving) deficiency", "Congenital lipoid adrenal hyperplasia due to STAR deficency", "congenital lipoid adrenal hyperplasia due to STAR deficency", "Cholesterol monooxygenase (side-chain cleaving) deficiency (disorder)", "Congenital lipoid hyperplasia of adrenal cortex with male pseudohermaphroditism", "Lipoid hyperplasia, congenital, of adrenal cortex with male pseudohermaphroditism", "lipoid hyperplasia, congenital, of adrenal cortex with Male pseudohermaphroditism", "LIPOID HYPERPLASIA, CONGENITAL, OF ADRENAL CORTEX WITH MALE PSEUDOHERMAPHRODITISM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital lipoid adrenal hyperplasia due to STAR deficency", "shortest_name_length": 4}
{"curie": "UMLS:C1335106", "names": ["Old Burn Scar-Related Skin Squamous Cell Carcinoma", "Old Burn Scar-Related Squamous Cell Carcinoma of Skin", "Old Burn Scar-Related Squamous Cell Carcinoma of the Skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Old Burn Scar-Related Skin Squamous Cell Carcinoma", "shortest_name_length": 50}
{"curie": "UMLS:C4526901", "names": ["Stage IA Soft Tissue Sarcoma of the Trunk and Extremities", "Stage IA Soft Tissue Sarcoma of the Trunk and Extremities AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Soft Tissue Sarcoma of the Trunk and Extremities AJCC v8", "shortest_name_length": 57}
{"curie": "UMLS:C0877429", "names": ["Anemia of malignant disease", "Anaemia of malignant disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anemia of malignant disease", "shortest_name_length": 27}
{"curie": "MONDO:0004507", "names": ["Breast Atypical Papilloma", "Atypical Breast Papilloma", "atypical breast papilloma", "Intraductal Breast Papilloma with Atypia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical breast papilloma", "shortest_name_length": 25}
{"curie": "MONDO:0005809", "names": ["Mousepox", "Mouse Pox", "Ectromelia virus", "Mousepox (disorder)", "Infectious Ectromelia", "infectious ectromelia", "Infectious ectromelia", "Ectromelia, Infectious"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infectious ectromelia", "shortest_name_length": 8}
{"curie": "UMLS:C3670571", "names": ["Pituitary hyperplasia", "Pituitary Hyperplasia", "Pituitary Gland Hyperplasia", "Pituitary gland hyperplastic", "Hyperplasia of pituitary gland", "Hyperplasia of pituitary gland (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyperplasia of pituitary gland", "shortest_name_length": 21}
{"curie": "UMLS:C0549493", "names": ["ALVEOLITIS", "Alveolitis", "alveolitis", "Alveolitis NOS", "ALVEOLITIS NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alveolitis", "shortest_name_length": 10}
{"curie": "MONDO:0042493", "names": ["stomach non-Hodgkin lymphoma", "gastric non-hodgkin lymphoma", "gastric non-Hodgkin lymphoma", "Gastric Non-Hodgkin Lymphoma", "non-Hodgkins gastric lymphoma", "Gastric Non-Hodgkin's Lymphoma", "gastric non-Hodgkin's lymphoma", "non-Hodgkin lymphoma of stomach", "Non-Hodgkin lymphoma of stomach", "non-Hodgkin's lymphoma of stomach", "Non-Hodgkin's lymphoma of stomach", "Non-Hodgkin's Lymphoma of Stomach", "lymphoma, gastric non Hodgkins type", "stomach lymphoma, non-Hodgkins type", "Primary Gastric Non-Hodgkin Lymphoma", "non-Hodgkin's lymphoma of the stomach", "Non-Hodgkin's Lymphoma of the Stomach", "Primary Gastric Non-Hodgkin's Lymphoma", "primary gastric non-Hodgkin's lymphoma", "Non-Hodgkin's lymphoma of stomach (disorder)", "non-Hodgkin's lymphoma of stomach (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric non-hodgkin lymphoma", "shortest_name_length": 28}
{"curie": "MONDO:0004332", "names": ["lung hilum cancer", "lung hilus cancer", "cancer of lung hilus", "malignant lung hilum tumor", "malignant hilar lung tumor", "Malignant Hilar Lung Tumor", "Malignant Lung Hilum Tumor", "Malignant Hilar Lung Neoplasm", "malignant lung hilus neoplasm", "malignant tumor of lung hilum", "malignant lung hilum neoplasm", "malignant hilar lung neoplasm", "Malignant Tumor of Lung Hilum", "Malignant Lung Hilum Neoplasm", "malignant tumor of lung Hilum", "malignant neoplasm of lung hilum", "malignant neoplasm of lung hilus", "malignant tumor of hilus of lung", "Malignant Neoplasm of Lung Hilum", "Malignant Tumor of the Lung Hilum", "malignant tumor of the lung hilum", "malignant neoplasm of hilus of lung", "Malignant neoplasm of hilus of lung", "Malignant Neoplasm of the Lung Hilum", "malignant neoplasm of the lung hilum", "Malignant neoplasm of hilus (of lung)", "lung neoplasm malignant hilus primary", "Primary malignant neoplasm of hilus of lung", "primary malignant neoplasm of hilus of lung", "malignant neoplasm of hilus of lung (diagnosis)", "Primary malignant neoplasm of hilus of lung (disorder)", "Primary malignant neoplasm of hilus of lung (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung hilum cancer", "shortest_name_length": 17}
{"curie": "UMLS:C5555711", "names": ["Recurrent Malignant Abdominal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Malignant Abdominal Neoplasm", "shortest_name_length": 38}
{"curie": "MONDO:0019970", "names": ["Osteochondrosis of patella", "aseptic necrosis of patella", "Sinding-Larsen-Johansson disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinding-Larsen-Johansson disease", "shortest_name_length": 26}
{"curie": "MONDO:0019931", "names": ["Leydig cell hypoplasia type II", "46,XY DSD due to partial LH resistance", "46,XY DSD due to partial LH receptor inactivation", "Leydig cell hypoplasia due to partial LH resistance", "46,XY DSD due to partial luteinizing hormone resistance", "Leydig cell hypoplasia due to partial LH receptor inactivation", "46,XY disorder of sex developement due to partial LH resistance", "Leydig cell hypoplasia due to partial luteinizing hormone resistance", "46,XY disorder of sex developement due to partial LH receptor inactivation", "Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation", "46,XY disorder of sex developement due to partial luteinizing hormone resistance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leydig cell hypoplasia due to partial LH resistance", "shortest_name_length": 30}
{"curie": "MONDO:0004105", "names": ["Epithelioid Sarcoma", "epithelioid sarcoma", "Pediatric Epithelioid Sarcoma", "pediatric epithelioid sarcoma", "Childhood Epithelioid Sarcoma", "childhood epithelioid sarcoma", "epithelioid sarcoma, childhood", "sarcoma, epithelioid, childhood", "epithelioid sarcoma of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood epithelioid sarcoma", "shortest_name_length": 19}
{"curie": "UMLS:C0677688", "names": ["Stage II Grade 2 Follicular Lymphoma", "contiguous stage II grade 2 follicular lymphoma", "Stage II Grade 2 Contiguous Follicular Lymphoma", "Contiguous Stage II Grade II Follicular Lymphoma", "Contiguous Grade II Follicular Lymphoma Stage II", "Contiguous Stage II Follicular Mixed Cell Lymphoma", "Stage II Contiguous Follicular Mixed Cell Lymphoma", "Contiguous Follicular Mixed Cell Lymphoma Stage II", "Ann Arbor Stage II Grade 2 Contiguous Follicular Lymphoma", "Contiguous Grade II Follicular Mixed Cell Lymphoma Stage II", "Contiguous Stage II Grade II Follicular Mixed Cell Lymphoma", "contiguous stage II grade II follicular mixed cell lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage II Grade 2 Contiguous Follicular Lymphoma", "shortest_name_length": 36}
{"curie": "MONDO:0035406", "names": ["furuncular myiasis due to Dermatobia hominis", "furunculoid myiasis due to Dermatobia hominis", "furunculous myiasis due to Dermatobia hominis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "furuncular myiasis due to Dermatobia hominis", "shortest_name_length": 44}
{"curie": "UMLS:C0235492", "names": ["RAYNAUD-LIKE DISORDER", "Raynaud like disorder", "Raynaud-like disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Raynaud like disorder", "shortest_name_length": 21}
{"curie": "MONDO:0001197", "names": ["Glanzmann", "Thrombocytopathy", "defect; platelets", "platelets; defect", "qualitative platelet defect", "Qualitative platelet defect", "Qualitative Platelet Defect", "Qualitative platelet defects", "Platelet disease, qualitative", "Qualitative Platelet Disorder", "Qualitative platelet disorder", "qualitative platelet deficiency", "Qualitative platelet deficiency", "Qualitative platelet disorder, NOS", "qualitative platelet defect (diagnosis)", "Qualitative platelet disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative platelet defect", "shortest_name_length": 9}
{"curie": "MONDO:0017953", "names": ["Reimann Periodic Disease", "Hereditary periodic fever", "Reimann Periodic Diseases", "Periodic Disease, Reimann", "Disease, Reimann Periodic", "Periodic Diseases, Reimann", "Diseases, Reimann Periodic", "Hereditary Recurrent Fever", "Siegal-Cattan-Mamou Disease", "Siegal Cattan Mamou Disease", "Fever, Hereditary Recurrent", "Recurrent Fever, Hereditary", "Hereditary Recurrent Fevers", "Recurrent Fevers, Hereditary", "Disease, Siegal-Cattan-Mamou", "Fevers, Hereditary Recurrent", "hereditary periodic fever syndrome", "Hereditary periodic fever syndrome", "Hereditary Autoinflammatory Disease", "Hereditary Autoinflammation Disease", "Hereditary Periodic Fever Syndromes", "Hereditary Autoinflammation Diseases", "Autoinflammation Disease, Hereditary", "Hereditary periodic fever (disorder)", "Autoinflammatory Disease, Hereditary", "Hereditary Autoinflammatory Diseases", "Disease, Hereditary Autoinflammatory", "Disease, Hereditary Autoinflammation", "Diseases, Hereditary Autoinflammation", "Autoinflammation Diseases, Hereditary", "Diseases, Hereditary Autoinflammatory", "Autoinflammatory Diseases, Hereditary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary periodic fever syndrome", "shortest_name_length": 24}
{"curie": "MONDO:0024638", "names": ["pancreatic gastrinoma", "Pancreatic Gastrinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic gastrinoma", "shortest_name_length": 21}
{"curie": "MONDO:0100282", "names": ["SC phocomelia syndrome", "hypomelia hypotrichosis facial hemangioma syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SC phocomelia syndrome", "shortest_name_length": 22}
{"curie": "UMLS:C3897248", "names": ["Umbilical Vasculitis", "Acute Umbilical Vasculitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Umbilical Vasculitis", "shortest_name_length": 20}
{"curie": "UMLS:C0521786", "names": ["Neonatal hearing loss", "Neonatal Hearing Loss", "Neonatal hearing loss (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neonatal hearing loss", "shortest_name_length": 21}
{"curie": "MONDO:0006365", "names": ["Peutz Jeghers polyp", "Peutz Jeghers Polyp", "Peutz Jehgers polyp", "Peutz-Jeghers Polyp", "Peutz-Jeghers polyp", "Peutz Jeghers polyp (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peutz-Jeghers polyp", "shortest_name_length": 19}
{"curie": "UMLS:C0345138", "names": ["PERICARDIAL DEFECT", "Pericardial defect", "pericardial defect", "Pericardial anomaly", "Pericardial Anomaly", "PERICARDIUM, DEFECT", "Pericardial defect (disorder)", "Pericardial anomaly (disorder)", "pericardial defect (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pericardial anomaly", "shortest_name_length": 18}
{"curie": "MONDO:0001232", "names": ["osteomyelitis; orbit", "orbit; osteomyelitis", "Orbital osteomyelitis", "orbital osteomyelitis", "Osteomyelitis of orbit", "Orbital osteomyelitis (disorder)", "orbital osteomyelitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orbital osteomyelitis", "shortest_name_length": 20}
{"curie": "MONDO:0006228", "names": ["Papillary adenocarcinoma", "Gastric Papillary Adenocarcinoma", "Papillary adenocarcinoma gastric", "stomach papillary adenocarcinoma", "papillary stomach adenocarcinoma", "gastric papillary adenocarcinoma", "Papillary adenocarcinoma of stomach", "papillary adenocarcinoma of stomach", "Papillary Adenocarcinoma of Stomach", "Papillary Adenocarcinoma of the Stomach", "papillary adenocarcinoma of the stomach", "papillary adenocarcinoma of stomach (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric papillary adenocarcinoma", "shortest_name_length": 24}
{"curie": "MONDO:0002047", "names": ["Scleroderma of lung", "scleroderma of lung", "Scleroderma lung disease", "scleroderma lung disease", "pulmonary systemic sclerosis", "lung disease with systemic sclerosis", "Bilateral basilar pulmonary fibrosis", "Lung disease with systemic sclerosis", "Lung involvement in systemic sclerosis", "lung involvement in systemic sclerosis", "Systemic sclerosis with lung involvement", "Lung disease with systemic sclerosis (disorder)", "lung; disease, in systemic sclerosis (etiology)", "lung; disease, in systemic sclerosis (manifestation)", "sclerosis; systemic, with lung involvement (etiology)", "systemic; sclerosis, with lung involvement (etiology)", "systemic; sclerosis, with lung involvement (manifestation)", "sclerosis; systemic, with lung involvement (manifestation)", "disease (or disorder); lung, in systemic sclerosis (etiology)", "disease (or disorder); lung, in systemic sclerosis (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary systemic sclerosis", "shortest_name_length": 19}
{"curie": "MONDO:0002440", "names": ["Renal polycythemia", "Renal polycythaemia", "nephrogenous polycythemia", "Nephrogenous polycythemia", "polycythemia; nephrogenous", "Polycythemia, nephrogenous", "Nephrogenous polycythaemia", "polycythemia, nephrogenous", "nephrogenous; polycythemia", "erythropoietin polycythemia", "Erythropoietin polycythemia", "erythropoietic polycythemia", "polycythemia; erythropoietin", "erythropoietin; polycythemia", "Polycythemia, erythropoietin", "secondary polycythemia erythropoietic", "erythropoietic polycythemia (diagnosis)", "Secondary polycythemia with excess erythropoietin", "secondary polycythemia with excess erythropoietin", "Secondary polycythaemia with excess erythropoietin", "Polycythemia due to excess erythopoetin production", "polycythemia due to excess erythopoetin production", "Polycythaemia due to excess erythopoetin production", "polycythaemia due to Excess erythropoetin production", "Polycythaemia due to Excess Erythropoetin Production", "Secondary polycythemia with excess erythropoietin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythropoietin polycythemia", "shortest_name_length": 18}
{"curie": "MONDO:0005483", "names": ["chemotherapy-induced alopecia", "Chemotherapy-Induced Alopecia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chemotherapy-induced alopecia", "shortest_name_length": 29}
{"curie": "MONDO:0014706", "names": ["ADCL3", "autosomal dominant cutis laxa 3", "cutis laxa, autosomal dominant 3", "CUTIS LAXA, AUTOSOMAL DOMINANT 3", "cutis laxa, autosomal dominant type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutis laxa, autosomal dominant 3", "shortest_name_length": 5}
{"curie": "MONDO:0018463", "names": ["mild PRPS1 superactivity", "mild PRPP synthetase superactivity", "mild phosphoribosylpyrophosphate synthetase superactivity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mild phosphoribosylpyrophosphate synthetase superactivity", "shortest_name_length": 24}
{"curie": "UMLS:C5236019", "names": ["Locally Advanced Renal Pelvis and Ureter Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Renal Pelvis and Ureter Urothelial Carcinoma", "shortest_name_length": 61}
{"curie": "UMLS:C2930844", "names": ["Hypopituitarism and septooptic 'dysplasia'"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypopituitarism and septooptic 'dysplasia'", "shortest_name_length": 42}
{"curie": "UMLS:C4289909", "names": ["Broad Ligament Serous Adenocarcinoma", "High-Grade Broad Ligament Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Broad Ligament Serous Adenocarcinoma", "shortest_name_length": 36}
{"curie": "MONDO:0010838", "names": ["GONADAL AGENESIS", "gonadal agenesis", "Gonadal Agenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gonadal agenesis", "shortest_name_length": 16}
{"curie": "MONDO:0004487", "names": ["endometrial type cervical adenomyoma", "Cervical Adenomyoma, Mesonephric-Type", "Cervical Adenomyoma, Mesonephric Type", "cervical adenomyoma, endometrial type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometrial type cervical adenomyoma", "shortest_name_length": 36}
{"curie": "MONDO:0008561", "names": ["thumb deformity", "THUMB DEFORMITY", "Thumb deformity", "deformity; thumb", "thumb; deformity", "thumb hypoplastic", "deformity of thumb", "Deformity of thumb", "Thumb abnormalities", "Abnormality of the thumb", "Abnormal thumb morphology", "thumb deformity (disease)", "Abnormality of the thumbs", "thumb absent or hypoplastic", "Deformity of thumb (finding)", "deformity of thumb (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thumb deformity", "shortest_name_length": 15}
{"curie": "UMLS:C0280627", "names": ["stage IV uterine sarcoma", "Stage IV Uterine Sarcoma", "uterine sarcoma, stage IV", "metastatic uterine sarcoma", "uterine sarcoma, metastatic", "Stage IV Uterine Sarcoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Uterine Sarcoma AJCC v7", "shortest_name_length": 24}
{"curie": "UMLS:C1142172", "names": ["Incision site complication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Incision site complication", "shortest_name_length": 26}
{"curie": "MONDO:0030749", "names": ["JEB3B", "epidermolysis bullosa, junctional 3B, severe", "EPIDERMOLYSIS BULLOSA, JUNCTIONAL 3B, SEVERE", "epidermolysis bullosa, junctional 3B, herlitz IIA", "EPIDERMOLYSIS BULLOSA, JUNCTIONAL 3B, HERLITZ TYPE", "EPIDERMOLYSIS BULLOSA, JUNCTIONAL 3B, GENERALIZED SEVERE", "epidermolysis bullosa, junctional 3B, generalized severe"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolysis bullosa, junctional 3B, severe", "shortest_name_length": 5}
{"curie": "MONDO:0008188", "names": ["carp", "CARP", "Gougerot-Carteaud", "Gougerot-Carteaud disease", "Gougerot-Carteaud syndrome", "gougerot-carteaud syndrome", "gougerot carteaud syndrome", "Papillomatosis, Familial Cutaneous", "papillomatosis, familial cutaneous", "PAPILLOMATOSIS, FAMILIAL CUTANEOUS", "Gougerot-Carteaud syndrome or disease", "Confluent and Reticulate Papillomatosis", "confluent and reticulate papillomatosis", "Confluent and reticulate papillomatosis", "Confluent AND reticulate papillomatosis", "Confluent and reticulated papillomatosis", "PAPILLOMATOSIS, CONFLUENT AND RETICULATED", "papillomatosis; confluent and reticulated", "papillomatosis, confluent and reticulated", "confluent and reticulated; papillomatosis", "Confluent AND reticulate papillomatosis (disorder)", "confluent and reticulate papillomatosis (diagnosis)", "Confluent and reticulate papillomatosis of Gougerot and Carteaud", "Confluent and reticulated papillomatosis of Gougerot and Carteaud", "papillomatosis, reticulated and confluent, of Gougerot and Carteaud", "PAPILLOMATOSIS, RETICULATED AND CONFLUENT, OF GOUGEROT AND CARTEAUD"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papillomatosis, confluent and reticulated", "shortest_name_length": 4}
{"curie": "MONDO:0021069", "names": ["Endocrine tumor", "Endocrine Tumor", "cancer endocrine", "endocrine cancer", "Endocrine neoplasm", "Endocrine Neoplasm", "endocrine neoplasm", "Neoplasm;endocrine", "endocrine neoplasms", "Endocrine neoplasia", "endocrine neoplasia", "ENDOCRINE NEOPLASIA", "Endocrine Neoplasms", "endocrine; neoplasia", "neoplasia; endocrine", "Endocrine cancer, NOS", "Endocrine neoplasm NOS", "endocrine gland cancer", "endocrine gland tumors", "Endocrine System Tumor", "endocrine system tumour", "endocrine gland tumours", "Tumor of endocrine gland", "Neoplasm malig;endocrine", "Endocrine glands--Tumors", "Endocrine Gland Neoplasm", "Tumor of endocrine system", "malignant endocrine tumor", "Endocrine Gland Neoplasms", "Tumour of endocrine gland", "Tumor of endocrine glands", "endocrine system neoplasm", "Malignant Endocrine Tumor", "malignant Endocrine tumor", "neoplasm of the endocrine", "Endocrine System Neoplasm", "endocrine tumor or cancer", "Neoplasm, Endocrine Gland", "cancer of endocrine gland", "Tumour of endocrine system", "Neoplasms, Endocrine Gland", "Neoplasm of endocrine gland", "neoplasm of endocrine gland", "Neoplasm of endocrine system", "neoplasm of endocrine system", "malignant endocrine neoplasm", "Malignant Endocrine Neoplasm", "Endocrine neoplasm malignant", "Endocrine Neoplasm, Malignant", "Endocrine Neoplasms Malignant", "endocrine neoplasm, malignant", "endocrine neoplasm (diagnosis)", "malignant endocrine gland tumor", "Malignant Endocrine Gland Tumor", "Neoplasm of the endocrine system", "Malignant endocrine neoplasm NOS", "Endocrine neoplasm malignant NOS", "Malignant Tumor of Endocrine Gland", "Malignant tumor of endocrine gland", "malignant endocrine gland neoplasm", "malignant tumor of endocrine gland", "Malignant Endocrine Gland Neoplasm", "Malignant tumour of endocrine gland", "malignant tumour of endocrine gland", "malignant neosplasm of the endocrine", "Malignant Neoplasm of Endocrine Gland", "Malignant neoplasm of endocrine gland", "malignant neoplasm of endocrine gland", "Neoplasm of endocrine gland (disorder)", "malignant tumor of the endocrine gland", "Malignant Tumor of the Endocrine Gland", "malignant neoplasm of endocrine glands", "Neoplasm of endocrine system (disorder)", "malignant neoplasm of the endocrine gland", "Malignant Neoplasm of the Endocrine Gland", "Malignant neoplasm of endocrine gland, NOS", "Malignant neoplasm of endocrine gland (disorder)", "malignant neoplasm of endocrine glands (diagnosis)", "Malignant neoplasm of endocrine gland, unspecified", "Malignant neoplasm of endocrine gland, site unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant endocrine neoplasm", "shortest_name_length": 15}
{"curie": "UMLS:C0333872", "names": ["Severe Squamous Cell Atypia", "Severe squamous cell atypia", "Severe squamous cell atypia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Severe squamous cell atypia", "shortest_name_length": 27}
{"curie": "UMLS:C0815316", "names": ["b12 deficiency anemia", "ANEMIA B12 DEFICIENCY", "B12 DEFICIENCY ANEMIA", "Anemia B12 deficiency", "anemia b12 deficiency", "B12 deficiency anemia", "B12 deficiency anaemia", "Anaemia B12 deficiency", "Anemia B twelve deficiency", "ANEMIA B TWELVE DEFICIENCY", "Anaemia B twelve deficiency", "Anemia cobalamin deficiency", "ANEMIA COBALAMIN DEFICIENCY", "ANAEMIA B TWELVE DEFICIENCY", "Anaemia cobalamin deficiency", "vitamin B12 deficiency anemia", "anemia vitamin b12 deficiency", "Vitamin B12 deficiency anemia", "vitamin b12 deficiency anemia", "Anemia vitamin B12 deficiency", "ANEMIA DEFICIENCY VITAMIN B12", "ANEMIA, VITAMIN B12 DEFICIENCY", "Vitamin B12 deficiency anaemia", "vitamin B12 deficiency anaemia", "Anaemia vitamin B12 deficiency", "anemia; deficiency vitamin B12", "vitamin b12 deficiency anaemia", "anaemia b12 deficiency vitamin", "Anaemia;vitamin B12 deficiency", "vitamin b 12 deficiency anemia", "Vitamin B>12< deficiency anemia", "Vitamin B>12< deficiency anaemia", "Vitamin B<sub>12</sub> deficiency anemia", "Vitamin B<sub>12</sub> deficiency anaemia", "Vitamin B12 deficiency anemia, unspecified", "Vitamin B12-deficient megaloblastic anemia", "Megaloblastic anemia due to B12 deficiency", "Vitamin B12-deficient megaloblastic anaemia", "Vitamin B12 deficiency anaemia, unspecified", "Megaloblastic anemia due to cobalamin deficiency", "Megaloblastic anaemia due to cobalamin deficiency", "Megaloblastic anemia due to vitamin B12 deficiency", "anemia megaloblastic due to vitamin B12 deficiency", "megaloblastic anemia due to vitamin B12 deficiency", "Megaloblastic anaemia due to vitamin B12 deficiency", "Megaloblastic anemia due to vitamin B>12< deficiency", "Megaloblastic anaemia due to vitamin B>12< deficiency", "Megaloblastic anemia due to vitamin B12 deficiency (disorder)", "Megaloblastic anemia due to vitamin B<sub>12</sub> deficiency", "megaloblastic anemia due to vitamin B12 deficiency (diagnosis)", "Megaloblastic anaemia due to vitamin B<sub>12</sub> deficiency", "Megaloblastic anemia due to vitamin B>12< deficiency (disorder)", "Megaloblastic anemia due to vitamin B<sub>12</sub> deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Megaloblastic anemia due to vitamin B>12< deficiency", "shortest_name_length": 21}
{"curie": "UMLS:C0746341", "names": ["Recurrent Hodgkin Lymphoma", "LYMPHOMA HODGKIN RECURRENT", "Recurrent Hodgkin's Disease", "Hodgkin's disease recurrent", "Recurrent Hodgkin's Lymphoma", "Hodgkin's disease NOS recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Hodgkin Lymphoma", "shortest_name_length": 26}
{"curie": "UMLS:C1697748", "names": ["Arteritis infective", "infective arteritis", "Infectious Arteritis", "infective arteritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infectious Arteritis", "shortest_name_length": 19}
{"curie": "MONDO:0060627", "names": ["GPIBD15", "GPAA1-related biosynthesis defect", "glycosylphosphatidylinositol biosynthesis defect 15", "GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15", "developmental delay, epilepsy, cerebellar atrophy, and osteopenia", "DEVELOPMENTAL DELAY, EPILEPSY, CEREBELLAR ATROPHY, AND OSTEOPENIA", "Glycosylphosphatidylinositol anchor attachment 1-related biosynthesis defect", "Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome", "Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome", "Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycosylphosphatidylinositol biosynthesis defect 15", "shortest_name_length": 7}
{"curie": "MONDO:0012514", "names": ["HLD5", "FAM126A leukodystrophy", "hypomyelinating leukodystrophy 5", "Leukodystrophy, Hypomyelinating, 5", "LEUKODYSTROPHY, HYPOMYELINATING, 5", "leukodystrophy, hypomyelinating, 5", "hypomyelination - congenital cataract", "hypomyelinating leukodystrophy type 5", "leukodystrophy, hypomyelinating, type 5", "Hypomyelination And Congenital Cataract", "Hypomyelination and congenital cataract", "hypomyelination and congenital cataract", "HYPOMYELINATION AND CONGENITAL CATARACT", "leukodystrophy caused by mutation in FAM126A", "Hypomyelination-congenital cataract syndrome", "hypomyelination and congenital cataract: HCC", "HYPOMYELINATION AND CONGENITAL CATARACT: HCC", "hypomyelination-congenital cataract syndrome", "HCC - hypomyelination and congenital cataract", "Hypomyelination and congenital cataract (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypomyelinating leukodystrophy 5", "shortest_name_length": 4}
{"curie": "MONDO:0035882", "names": ["CIUE", "chronic intervillositis of unknown etiology"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic intervillositis of unknown etiology", "shortest_name_length": 4}
{"curie": "MONDO:0013780", "names": ["RP63", "RETINITIS PIGMENTOSA 63", "retinitis pigmentosa 63", "retinitis pigmentosa type 63"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 63", "shortest_name_length": 4}
{"curie": "UMLS:C4329653", "names": ["Cervical and Thoracic Spinal Cord Ependymal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical and Thoracic Spinal Cord Ependymal Tumor", "shortest_name_length": 49}
{"curie": "MONDO:0018142", "names": ["pyruvate carboxylase deficiency type B", "pyruvate carboxylase deficiency, severe neonatal type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyruvate carboxylase deficiency, severe neonatal type", "shortest_name_length": 38}
{"curie": "MONDO:0005311", "names": ["ascvd", "Atheromatosis", "atheromatosis", "Atheroscleroses", "atheroscleroses", "ATHEROSCLEROSIS", "atherosclerosis", "Atherosclerosis", "Atheromatosis, NOS", "AS - Atherosclerosis", "Atherosclerosis, NOS", "atherosclerosis artery", "Atherosclerosis artery", "Atherosclerosis of artery", "atherosclerosis of artery", "atherosclerosis (diagnosis)", "Plaque build-up in arteries", "ATHEROSCLEROTIC VASCULAR DISEASE", "atherosclerotic vascular disease", "VASCULAR DISEASE ATHEROSCLEROTIC", "Narrowing and hardening of arteries", "Atherosclerosis of artery (disorder)", "Atherosclerotic cardiovascular disease", "Atherosclerotic Cardiovascular Disease", "atherosclerotic cardiovascular disease", "Atherosclerosis (morphologic abnormality)", "Atherosclerotic cardiovascular disease, so described"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atherosclerosis", "shortest_name_length": 5}
{"curie": "UMLS:C1335012", "names": ["Non-Neoplastic Gonadal Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Gonadal Disorder", "shortest_name_length": 31}
{"curie": "MONDO:0014397", "names": ["COXPD20", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 20", "combined oxidative phosphorylation deficiency 20", "combined oxidative phosphorylation defect type 20", "Combined oxidative phosphorylation defect type 20", "VARS2 combined oxidative phosphorylation deficiency", "combined oxidative phosphorylation deficiency type 20", "combined oxidative phosphorylation deficiency caused by mutation in VARS2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation defect type 20", "shortest_name_length": 7}
{"curie": "UMLS:C5447697", "names": ["Plaque-Like Dermatofibrosarcoma Protuberans"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Plaque-Like Dermatofibrosarcoma Protuberans", "shortest_name_length": 43}
{"curie": "MONDO:0015421", "names": ["OFD12", "OFDS 12", "Moran-Barroso syndrome", "Moran Barroso syndrome", "Orofaciodigital Syndrome 12", "orofaciodigital syndrome 12", "orofaciodigital syndrome XII", "oral-facial-digital syndrome 12", "oral facial digital syndrome 12", "orofaciodigital syndrome type 12", "Orofaciodigital syndrome type 12", "Oro-facial digital syndrome type 12", "oral-facial-digital syndrome type 12", "Oral-facial-digital syndrome type 12", "oral facial digital syndrome type 12", "Oro-facial digital syndrome type 12 (disorder)", "oral-facial-digital syndrome type 12 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orofaciodigital syndrome type 12", "shortest_name_length": 5}
{"curie": "MONDO:0013590", "names": ["STL4", "Stickler syndrome, type 4", "STICKLER syndrome, type IV", "STICKLER SYNDROME, TYPE IV", "COL9A1 autosomal recessive Stickler syndrome", "autosomal recessive Stickler syndrome caused by mutation in COL9A1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stickler syndrome, type 4", "shortest_name_length": 4}
{"curie": "MONDO:0014227", "names": ["COLED", "COLE DISEASE", "Cole disease", "COLE disease", "guttate hypopigmentation", "Hypopigmentation-punctate palmoplantar keratoderma syndrome", "hypopigmentation-punctate palmoplantar keratoderma syndrome", "Hypopigmentation and punctate keratosis of the palms and soles", "guttate hypopigmentation and punctate palmoplantar keratoderma", "hypopigmentation and punctate keratosis of the palms and soles", "Guttate hypopigmentation and punctate palmoplantar keratoderma", "punctate palmoplantar keratoderma with or without ectopic calcification", "GUTTATE HYPOPIGMENTATION AND PUNCTATE PALMOPLANTAR KERATODERMA WITH OR WITHOUT ECTOPIC CALCIFICATION", "guttate hypopigmentation and punctate palmoplantar keratoderma with or without ectopic calcification", "Guttate hypopigmentation and punctate palmoplantar keratoderma with or without ectopic calcification", "Guttate hypopigmentation and punctate palmoplantar keratoderma with or without ectopic calcification (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypopigmentation-punctate palmoplantar keratoderma syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0030330", "names": ["RCM6", "CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 6", "cardiomyopathy, familial restrictive, 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiomyopathy, familial restrictive, 6", "shortest_name_length": 4}
{"curie": "UMLS:C0856597", "names": ["Pulmonary Alveolitis", "Pulmonary alveolitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pulmonary alveolitis", "shortest_name_length": 20}
{"curie": "UMLS:C4684421", "names": ["PIK3CA-activated mutation", "PIK3CA Activating Mutation", "PIK3CA Activation Mutation", "Activating PIK3CA Gene Mutation", "Activating PI3KCA Gene Mutation", "PIK3CA Gain of Function Mutation", "Activating p110-alpha Gene Mutation", "Activating PI3K-Alpha Gene Mutation", "PIK3CA Gain of Function Gene Mutation", "Activating Phosphatidylinositol-4,5-Bisphosphate 3-Kinase Catalytic Subunit Alpha Gene Mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PIK3CA-activated mutation", "shortest_name_length": 25}
{"curie": "UMLS:C0855186", "names": ["Relapsed Bladder Epidermoid Carcinoma", "Recurrent Bladder Epidermoid Carcinoma", "Relapsed Epidermoid Carcinoma of Bladder", "Relapsed Bladder Squamous Cell Carcinoma", "Squamous cell bladder carcinoma recurrent", "Recurrent Bladder Squamous Cell Carcinoma", "Bladder squamous cell carcinoma recurrent", "Recurrent Epidermoid Carcinoma of Bladder", "Relapsed Squamous Cell Carcinoma of Bladder", "Recurrent Squamous Cell Carcinoma of Bladder", "Relapsed Epidermoid Carcinoma of the Bladder", "Recurrent Epidermoid Carcinoma of the Bladder", "Relapsed Urinary Bladder Epidermoid Carcinoma", "Squamous Cell Carcinoma of Bladder, Recurrent", "Recurrent Urinary Bladder Epidermoid Carcinoma", "Relapsed Squamous Cell Carcinoma of the Bladder", "Relapsed Epidermoid Carcinoma of Urinary Bladder", "Squamous cell carcinoma of the bladder recurrent", "Relapsed Urinary Bladder Squamous Cell Carcinoma", "Recurrent Squamous Cell Carcinoma of the Bladder", "Squamous Cell Carcinoma of the Bladder, Recurrent", "Recurrent Urinary Bladder Squamous Cell Carcinoma", "Recurrent Epidermoid Carcinoma of Urinary Bladder", "Relapsed Squamous Cell Carcinoma of Urinary Bladder", "Relapsed Epidermoid Carcinoma of the Urinary Bladder", "Recurrent Squamous Cell Carcinoma of Urinary Bladder", "Recurrent Epidermoid Carcinoma of the Urinary Bladder", "Relapsed Squamous Cell Carcinoma of the Urinary Bladder", "Recurrent Squamous Cell Carcinoma of the Urinary Bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder squamous cell carcinoma recurrent", "shortest_name_length": 37}
{"curie": "UMLS:C0161446", "names": ["Brachial plexus injury", "brachial injury plexus", "brachial plexus injury", "Brachial Plexus Injury", "BRACHIAL PLEXUS INJURY", "injury; brachial plexus", "Brachial Plexus Injuries", "brachial injuries plexus", "Injury of brachial plexus", "plexus brachialis; injury", "injury of brachial plexus", "of brachial plexus injury", "Injury to brachial plexus", "Traumatic brachial plexus lesion", "Injury of brachial plexus (disorder)", "injury to brachial plexus nerve root", "injury of brachial plexus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of brachial plexus", "shortest_name_length": 22}
{"curie": "UMLS:C0341134", "names": ["Radiation-Induced Esophageal Stricture", "Radiation-Induced Stricture of Esophagus", "Radiation-induced stricture of esophagus", "Radiation-induced stricture of oesophagus", "Radiation-induced stricture of esophagus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radiation-induced stricture of esophagus", "shortest_name_length": 38}
{"curie": "MONDO:0019500", "names": ["extragonadal teratoma", "Extragonadal Teratoma", "Extragonadal teratoma", "teratoma extragonadal", "Extragonadal teratoma (disorder)", "Extragonadal teratoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extragonadal teratoma", "shortest_name_length": 21}
{"curie": "MONDO:0003097", "names": ["Pediatric Mediastinal Neurogenic Tumor", "Childhood Mediastinal Neurogenic Tumor", "pediatric mediastinal neurogenic tumor", "childhood mediastinal neurogenic tumor", "childhood mediastinal neurogenic tumour", "Childhood Neurogenic Tumor of Mediastinum", "pediatric neurogenic tumor of mediastinum", "childhood neurogenic tumor of mediastinum", "Pediatric Neurogenic Tumor of Mediastinum", "Pediatric Mediastinal Neurogenic Neoplasm", "Childhood Mediastinal Neurogenic Neoplasm", "pediatric mediastinal neurogenic neoplasm", "childhood mediastinal neurogenic neoplasm", "paediatric neurogenic tumour of mediastinum", "childhood neurogenic neoplasm of mediastinum", "Pediatric Neurogenic Neoplasm of Mediastinum", "Childhood Neurogenic Neoplasm of Mediastinum", "pediatric neurogenic neoplasm of mediastinum", "childhood neurogenic tumor of the mediastinum", "pediatric neurogenic tumor of the mediastinum", "Childhood Neurogenic Tumor of the Mediastinum", "Pediatric Neurogenic Tumor of the Mediastinum", "childhood neurogenic neoplasm of the mediastinum", "Childhood Neurogenic Neoplasm of the Mediastinum", "pediatric neurogenic neoplasm of the mediastinum", "Pediatric Neurogenic Neoplasm of the Mediastinum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood mediastinal neurogenic neoplasm", "shortest_name_length": 38}
{"curie": "MONDO:0012695", "names": ["MKS5", "Meckel syndrome 5", "Meckel syndrome type 5", "Meckel Syndrome, Type 5", "Meckel syndrome, type 5", "MECKEL SYNDROME, TYPE 5", "RPGRIP1L Meckel syndrome", "Meckel-Gruber syndrome, type 5", "Meckel syndrome type 5 (diagnosis)", "Meckel syndrome caused by mutation in RPGRIP1L"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meckel syndrome, type 5", "shortest_name_length": 4}
{"curie": "MONDO:0020487", "names": ["pontiac fever", "Pontiac fever", "Pontiac Fever", "Fever, Pontiac", "fever; Pontiac", "Pontiac; fever", "Pontiac fever (disorder)", "pontiac fever (diagnosis)", "Legionella pneumophila; infection, nonpneumonic", "infection; Legionella pneumophila, nonpneumonic", "disease (or disorder); legionnaire's, nonpneumonic", "Nonpneumonic Legionnaires' disease [Pontiac fever]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pontiac fever", "shortest_name_length": 13}
{"curie": "MONDO:0042487", "names": ["CIN3", "cin 3", "CIN 3", "CIN III", "cin iii", "CIN, III, NOS", "CIN 3 aJCC v6", "CIN 3 AJCC v6", "CIS of cervix", "Cervix Ca in situ", "cervix Ca in situ", "CIN grade 3 aJCC v6", "CIN Grade 3 AJCC v6", "carcinoma cervix situ", "stage 0 cervix cancer", "cervix cancer, stage 0", "CERVICAL CANCER CIN III", "stage 0 cervical cancer", "Stage 0 Cervical Cancer", "Cervical cancer stage 0", "Cervix carcinoma in situ", "Carcinoma in situ;cervix", "CERVIX CARCINOMA IN SITU", "Carcinoma cervix in situ", "carcinoma in situ cervix", "Cervix carcinoma stage 0", "cervical cancer, stage 0", "In situ cancer of cervix", "cervix carcinoma in situ", "CARCINOMA CERVIX IN SITU", "carcinoma-in-situ cervix", "dysplasia; cervix, severe", "severe cervical dysplasia", "cervical carcinoma in situ", "Cervical carcinoma in situ", "severe dysplasia of cervix", "CERVICAL CARCINOMA IN SITU", "Cervical carcinoma stage 0", "cervical carcinoma stage 0", "Severe dysplasia of cervix", "Carcinoma in situ of cervix", "carcinoma in situ of cervix", "carcinoma of cervix stage 0", "stage 0 cancer of the cervix", "CIN III - severe dyskaryosis", "cancer of the cervix, stage 0", "FIGO Stage 0 Cervix Carcinoma", "FIGO stage 0 cervix carcinoma", "CIN III with severe dysplasia", "stage 0 uterine cervix cancer", "uterine cervix cancer, stage 0", "CIN, III with severe dysplasia", "cervix uteri carcinoma in situ", "Cervix Severe Dysplasia AJCC v6", "FIGO stage 0 cervical carcinoma", "Stage 0 Cervical Cancer AJCC v6", "stage 0 cervical cancer aJCC v6", "Cervical cancer stage 0 AJCC v6", "cervical cancer stage 0 aJCC v6", "cervix Severe dysplasia aJCC v6", "FIGO Stage 0 Cervical Carcinoma", "stage 0 carcinoma of the cervix", "carcinoma in situ of the cervix", "Cervix Carcinoma in situ AJCC v6", "Carcinoma uterine cervix in situ", "carcinoma of the cervix, stage 0", "FIGO stage 0 carcinoma of cervix", "stage 0 uterine cervix carcinoma", "uterine cervix carcinoma in situ", "Uterine cervix carcinoma stage 0", "cervix carcinoma in situ aJCC v6", "CARCINOMA UTERINE CERVIX IN SITU", "FIGO Stage 0 Carcinoma of Cervix", "uterine cervical cancer, stage 0", "cervical Severe dysplasia aJCC v6", "Cervical Severe Dysplasia AJCC v6", "severe cervical dysplasia aJCC v6", "carcinoma in situ of cervix uteri", "Carcinoma in situ of cervix uteri", "Severe Cervical Dysplasia AJCC v6", "CIS - Carcinoma in situ of cervix", "severe dysplasia of cervix aJCC v6", "cervical carcinoma in situ aJCC v6", "Severe Dysplasia of Cervix AJCC v6", "Cervical Carcinoma in situ AJCC v6", "carcinoma in situ of cervix aJCC v6", "severe cervical dysplasia (CIN III)", "Carcinoma in situ of Cervix AJCC v6", "FIGO Stage 0 Cervix Uteri Carcinoma", "FIGO stage 0 cervix uteri carcinoma", "carcinoma in situ of uterine cervix", "Carcinoma in situ of uterine cervix", "FIGO stage 0 carcinoma of the cervix", "Severe Dysplasia of the Cervix Uteri", "FIGO Stage 0 Carcinoma of the Cervix", "CIN III - carcinoma in situ of cervix", "FIGO stage 0 uterine cervix carcinoma", "FIGO Stage 0 Uterine Cervix Carcinoma", "cervix uteri Severe dysplasia aJCC v6", "severe cervical dysplasia (diagnosis)", "Cervix Uteri Severe Dysplasia AJCC v6", "FIGO stage 0 carcinoma of cervix uteri", "Cervical intraepithelial neoplasia III", "FIGO Stage 0 Carcinoma of Cervix Uteri", "cervical carcinoma stage 0 (diagnosis)", "severe dysplasia of the cervix aJCC v6", "Severe Dysplasia of the Cervix AJCC v6", "cervix uteri carcinoma in situ aJCC v6", "Cervix Uteri Carcinoma in situ AJCC v6", "uterine cervix Severe dysplasia aJCC v6", "Carcinoma in situ of the Cervix AJCC v6", "carcinoma in situ of the cervix aJCC v6", "Uterine Cervix Severe Dysplasia AJCC v6", "carcinoma in situ of cervix (diagnosis)", "Carcinoma in situ of cervix, unspecified", "Severe Dysplasia of Cervix Uteri AJCC v6", "Uterine Cervix Carcinoma in situ AJCC v6", "FIGO stage 0 carcinoma of uterine cervix", "severe dysplasia of cervix uteri aJCC v6", "FIGO Stage 0 Carcinoma of Uterine Cervix", "uterine cervix carcinoma in situ aJCC v6", "carcinoma in situ of cervix uteri aJCC v6", "Carcinoma in situ of Cervix Uteri AJCC v6", "cervical intraepithelial neoplasia grade 3", "Cervical intraepithelial neoplasia grade 3", "Severe Dysplasia of Uterine Cervix AJCC v6", "FIGO stage 0 carcinoma of the cervix uteri", "severe dysplasia of uterine cervix aJCC v6", "FIGO Stage 0 Carcinoma of the Cervix Uteri", "Carcinoma in situ of Uterine Cervix AJCC v6", "carcinoma in situ of uterine cervix aJCC v6", "FIGO Stage 0 Carcinoma of the Uterine Cervix", "Cervical intraepithelial neoplasia grade III", "severe dysplasia of the cervix uteri aJCC v6", "cervix; intraepithelial neoplasia, grade III", "FIGO stage 0 carcinoma of the uterine cervix", "Severe Dysplasia of the Cervix Uteri AJCC v6", "carcinoma in situ of cervix uteri (diagnosis)", "squamous intraepithelial neoplasia, grade III", "Cervical intraepithelial neoplasia, grade III", "Cervical Intraepithelial Neoplasia, Grade III", "[OBSOLETE] Cervical Intraepithelial Neoplasia", "carcinoma in situ of the cervix uteri aJCC v6", "neoplasia; intraepithelial, cervix, grade III", "Carcinoma in situ of the Cervix Uteri AJCC v6", "severe dysplasia of the uterine cervix aJCC v6", "Severe Dysplasia of the Uterine Cervix AJCC v6", "Carcinoma in situ of uterine cervix (disorder)", "Carcinoma in situ of the Uterine Cervix AJCC v6", "carcinoma in situ of the uterine cervix aJCC v6", "Cervix Intraepithelial Neoplasia Grade 3 AJCC v6", "cervix intraepithelial neoplasia grade 3 aJCC v6", "Cervical Intraepithelial Neoplasia Grade 3 AJCC v6", "Grade 3 Cervical Intraepithelial Neoplasia AJCC v6", "CIN 3 - Cervical intraepithelial neoplasia grade 3", "grade 3 cervical intraepithelial neoplasia aJCC v6", "cervical intraepithelial neoplasia grade 3 aJCC v6", "intraepithelial neoplasia of cervix grade 3 aJCC v6", "Intraepithelial Neoplasia of Cervix Grade 3 AJCC v6", "cervix uteri intraepithelial neoplasia grade 3 aJCC v6", "Cervix Uteri Intraepithelial Neoplasia Grade 3 AJCC v6", "Intraepithelial Neoplasia of the Cervix Grade 3 AJCC v6", "intraepithelial neoplasia of the cervix grade 3 aJCC v6", "uterine cervix intraepithelial neoplasia grade 3 aJCC v6", "Uterine Cervix Intraepithelial Neoplasia Grade 3 AJCC v6", "intraepithelial neoplasia of cervix uteri grade 3 aJCC v6", "Intraepithelial Neoplasia of Cervix Uteri Grade 3 AJCC v6", "intraepithelial neoplasia of uterine cervix grade 3 aJCC v6", "Intraepithelial Neoplasia of Uterine Cervix Grade 3 AJCC v6", "Intraepithelial Neoplasia of the Cervix Uteri Grade 3 AJCC v6", "intraepithelial neoplasia of the cervix uteri grade 3 aJCC v6", "intraepithelial neoplasia of the uterine cervix grade 3 aJCC v6", "Intraepithelial Neoplasia of the Uterine Cervix Grade 3 AJCC v6", "cervical intraepithelial neoplasia grade III with severe dysplasia", "Cervical intraepithelial neoplasia grade III with severe dysplasia", "CIN III - Cervical intraepithelial neoplasia grade III with severe dysplasia", "Cervical intraepithelial neoplasia grade III with severe dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine cervix carcinoma in situ", "shortest_name_length": 4}
{"curie": "MONDO:0011827", "names": ["PDA", "Ductus arteriosus", "d.arteriosus; open", "Patent arterial duct", "patent ductus botalli", "Patent ductus Botalli", "Patent Ductus Arteriosus", "Patent ductus arteriosus", "Persistent arterial duct", "d.arteriosus; persistent", "d.arteriosus; nonclosure", "arteriosus ductus patent", "arteriosis ductus patent", "patent ductus arteriosis", "patent ductus arteriosus", "PATENT DUCTUS ARTERIOSUS", "patent arteriosus ductus", "Ductus Arteriosus, Patent", "ductus arteriosus, Patent", "DUCTUS ARTERIOSUS, PATENT", "ductus arteriosus, patent", "Persistent ductus arteriosus", "persistent ductus arteriosus", "ductus arteriosus persistent", "nonclosure; ductus arteriosus", "PDA (patent ductus arteriosus)", "PDA - Patent ductus arteriosus", "Patency of the Ductus Arteriosus", "patency of the ductus arteriosus", "open; ductus arteriosus (Botalli)", "Patent ductus arteriosus (disorder)", "patent ductus arteriosus (diagnosis)", "persistent patency of the arterial duct", "persistent; ductus arteriosus (Botalli)", "patent ductus arteriosus familial (type)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "patent ductus arteriosus", "shortest_name_length": 3}
{"curie": "UMLS:C5446399", "names": ["Lacrimal Gland Carcinosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lacrimal Gland Carcinosarcoma", "shortest_name_length": 29}
{"curie": "MONDO:0018871", "names": ["M4", "AMML", "AMMoL", "AML-M4", "FAB M4", "AML M4", "AML M5a", "FAB M5A", "FAB type M5a", "Acute myelosis", "myelosis; acute", "acute; myelosis", "myeloblastic leukemia", "Myeloblastic leukemia", "myeloblastic; leukemia", "leukemia; myeloblastic", "Acute M4 Myeloid Leukemia", "Acute monocytoid leukemia", "m4 acute myeloid leukemia", "acute M4 myeloid leukemia", "Acute monoblastic leukemia", "Leukemia monoblastic acute", "acute monoblastic leukemia", "Acute Monoblastic Leukemia", "LEUKEMIA MONOBLASTIC ACUTE", "ACUTE MONOBLASTIC LEUKEMIA", "Acute monocytoid leukaemia", "Leukaemia monoblastic acute", "Acute monoblastic leukaemia", "Myeloid Leukemia, Acute, M4", "Leukemia, Myeloid, Acute, M4", "Naegeli-Type Myeloid Leukemia", "Acute myelomonocytic leukemia", "Blastic granulocytic leukemia", "acute myelomonocytic leukemia", "leukemia acute myelomonocytic", "Acute Myelomonocytic Leukemia", "Myeloid Leukemia, Naegeli-Type", "Myelomonocytic Leukemia, Acute", "Acute myelomonocytic leukaemia", "Leukemia, Naegeli-Type Myeloid", "Myeloid Leukemia, Naegeli Type", "Acute Myelomonocytic Leukemias", "Leukemia, Acute Myelomonocytic", "acute myelomonocytic leukaemia", "Leukemia, Myelomonocytic, Acute", "leukemia; myelomonocytic, acute", "Leukemia, Myeloid, Naegeli-Type", "granulocytic; leukemia, blastic", "blastic; leukemia, granulocytic", "Leukemias, Acute Myelomonocytic", "leukemia; blastic, granulocytic", "Naegeli-type monocytic leukemia", "Myelomonocytic Leukemias, Acute", "leukemia; granulocytic, blastic", "myelomonocytic; leukemia, acute", "French-American-British type M5a", "leukemia; Naegeli-type monocytic", "M5a - Acute monoblastic leukemia", "Naegeli-type monocytic leukaemia", "acute myelomonocytic leukemia M4", "Naegeli-type monocytic; leukemia", "monocytic; leukemia, Naegeli-type", "Acute myelomonocytic leukemia NOS", "M5a - Acute monoblastic leukaemia", "acute myeloblastic leukemia type 4", "M4 - Acute myelomonocytic leukemia", "M4 OR Acute Myelomonocytic Leukemia", "M4 - Acute myelomonocytic leukaemia", "Acute Monoblastic Leukemia (FAB M5a)", "AMML - Acute myelomonocytic leukemia", "Acute myelomonocytic leukemia, FAB M4", "Acute monoblastic leukemia (disorder)", "AMML - Acute myelomonocytic leukaemia", "Acute monoblastic leukemia (diagnosis)", "Acute myelomonocytic leukaemia, FAB M4", "Acute myelomonocytic leukemia (clinical)", "Acute myelomonocytic leukaemia (clinical)", "acute myelomonocytic leukemia (diagnosis)", "acute myelomonocytic leukemia (FAB type M4)", "Acute Myelomonocytic Leukemia (FAB Type M4)", "leukemia myelogenous acute (AML) monoblastic", "Acute myelomonocytic leukemia, FAB M4 (disorder)", "French-American-British type M5a (qualifier value)", "Acute myelomonocytic leukemia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myelomonocytic leukemia M4", "shortest_name_length": 2}
{"curie": "MONDO:0004861", "names": ["Ophthalmia nodosa", "ophthalmia nodosa", "ophthalmia; nodosa", "nodosa; ophthalmia", "Caterpillar ophthalmia", "Caterpillar-hair ophthalmia", "Ophthalmia nodosa (disorder)", "ophthalmia nodosa (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ophthalmia nodosa", "shortest_name_length": 17}
{"curie": "UMLS:C4520727", "names": ["Stage II Childhood Hepatoma", "Stage II Pediatric Hepatoma", "Stage II Hepatocellular Cancer", "stage II childhood liver cancer", "Stage II Pediatric Liver Cell Carcinoma", "Stage II Childhood Liver Cell Carcinoma", "Stage II Pediatric Hepatocellular Carcinoma", "Stage II Childhood Hepatocellular Carcinoma AJCC v6", "Stage II Childhood Hepatocellular Carcinoma AJCC v7", "Stage II Childhood Hepatocellular Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Childhood Hepatocellular Carcinoma AJCC v6 and v7", "shortest_name_length": 27}
{"curie": "MONDO:0007379", "names": ["MECD", "Meesman dystrophy", "Stocker-Holt dystrophy", "stocker-Holt dystrophy", "MEESMANN CORNEAL DYSTROPHY", "Meesmann corneal dystrophy", "Meesmann Corneal Dystrophy", "corneal dystrophy, Meesmann", "Corneal Dystrophy, Meesmann", "Meesman's corneal dystrophy", "Meesmann Corneal Dystrophies", "Dystrophies, Meesmann Corneal", "Corneal Dystrophies, Meesmann", "juvenile epithelial corneal dystrophy", "Juvenile epithelial corneal dystrophy", "Meesmann Epithelial Corneal Dystrophy", "Meesmann Corneal Epithelial Dystrophy", "Meesmann corneal epithelial dystrophy", "CORNEAL DYSTROPHY, MEESMANN EPITHELIAL", "Corneal Dystrophy, Meesmann Epithelial", "corneal dystrophy, Meesmann epithelial", "Meesman's epithelial corneal dystrophy", "Epithelial (juvenile) corneal dystrophy", "Juvenile Hereditary Epithelial Dystrophy", "juvenile hereditary epithelial dystrophy", "Juvenile epithelial corneal dystrophy (disorder)", "Juvenile Epithelial of Meesmann Corneal Dystrophy", "juvenile epithelial of Meesmann corneal dystrophy", "juvenile epithelial corneal dystrophy (diagnosis)", "Corneal Dystrophy, Juvenile Epithelial of Meesmann", "corneal dystrophy, juvenile epithelial of Meesmann", "corneal dystrophy, juvenile epithelial, of Meesmann", "CORNEAL DYSTROPHY, JUVENILE EPITHELIAL, OF MEESMANN", "Juvenile hereditary epithelial dystrophy of Meesmann", "juvenile hereditary epithelial dystrophy of Meesmann"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meesmann corneal dystrophy", "shortest_name_length": 4}
{"curie": "UMLS:C0032993", "names": ["post date", "post-dates", "Post-dates", "prolonged pregnancy", "Post-term pregnancy", "Prolonged Pregnancy", "Pregnancy;post term", "pregnancy post term", "post-term pregnancy", "Prolonged gestation", "post term pregnancy", "PREGNANCY PROLONGED", "Post term pregnancy", "Post Term Pregnancy", "Prolonged pregnancy", "Pregnancy, prolonged", "post-term; pregnancy", "pregnancy prolonging", "Pregnancy, Prolonged", "pregnancy; post-term", "postmature; pregnancy", "Prolonged Pregnancies", "pregnancy; postmature", "Pregnancy, Protracted", "Pregnancies, Prolonged", "pregnancy; prolonged pregnancy", "Prolonged pregnancy (disorder)", "prolonged pregnancy (diagnosis)", "Pregnancy beyond 42 weeks of gestation", "post-term pregnancy (40 to 42 weeks gestation)", "post-term pregnancy of 40 to 42 weeks gestation", "post-term pregnancy of 40 to 42 weeks gestation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pregnancy, Prolonged", "shortest_name_length": 9}
{"curie": "UMLS:C0853700", "names": ["Application site erythema", "Application site erythema (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Application site erythema", "shortest_name_length": 25}
{"curie": "MONDO:0016833", "names": ["Del(14)(q12)", "monosomy 14q12", "Monosomy 14q12", "14q12 microdeletion syndrome", "14q12 microdeletion syndrome (disorder)", "FOXG1 syndrome due to 14q12 microdeletion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "14q12 microdeletion syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0004837", "names": ["Esophagus Neurofibroma", "esophagus neurofibroma", "esophageal neurofibroma", "Esophageal Neurofibroma", "neurofibroma of esophagus", "Neurofibroma of Esophagus", "neurofibroma of the esophagus", "Neurofibroma of the Esophagus", "neurofibroma of esophagus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurofibroma of the esophagus", "shortest_name_length": 22}
{"curie": "UMLS:C1332055", "names": ["AIDS-Related Plasmablastic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Plasmablastic Lymphoma", "shortest_name_length": 35}
{"curie": "MONDO:0007702", "names": ["heart-hand syndrome type 3", "Heart-hand syndrome type 3", "Heart-limb syndrome type 3", "heart-limb syndrome type 3", "Heart limb syndrome type 3", "Cardiomelic syndrome type 3", "Atriodigital dysplasia type 3", "atriodigital dysplasia type 3", "Heart hand syndrome Spanish type", "heart-hand syndrome, Spanish type", "HEART-HAND SYNDROME, SPANISH TYPE", "Heart-hand syndrome, Spanish type", "Heart-hand syndrome type 3 (disorder)", "brachydactyly and intraventricular conduction defect", "Brachydactyly and intraventricular conduction defect", "upper limb malformations and congenital cardiac anomalies", "Upper limb malformations and congenital cardiac anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heart-hand syndrome type 3", "shortest_name_length": 26}
{"curie": "UMLS:C4727593", "names": ["Crooke Cell Tumor", "Crooke Cell Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Crooke Cell Tumor", "shortest_name_length": 17}
{"curie": "MONDO:0016666", "names": ["unexplained long-lasting fever/inflammatory syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "unexplained long-lasting fever/inflammatory syndrome", "shortest_name_length": 52}
{"curie": "UMLS:C4725818", "names": ["Recurrent Malignant Urinary System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Malignant Urinary System Neoplasm", "shortest_name_length": 43}
{"curie": "MONDO:0009637", "names": ["Ragged red myopathy", "MITOCHONDRIAL MYOPATHY", "Mitochondrial myopathy", "Mitochondrial Myopathy", "MYOPATHY MITOCHONDRIAL", "mitochondrial myopathy", "MYOPATHY, MITOCHONDRIAL", "Myopathy, mitochondrial", "Mitochondrial cytopathy", "mitochondrial; myopathy", "mitochondrial cytopathy", "myopathy; mitochondrial", "myopathies mitochondrial", "mitochondrial myopathies", "Mitochondrial Myopathies", "Myopathies, Mitochondrial", "cytopathies mitochondrial", "inborn mitochondrial myopathy", "Mitochondrial myopathy (disorder)", "mitochondrial myopathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn mitochondrial myopathy", "shortest_name_length": 19}
{"curie": "UMLS:C0341163", "names": ["Perforated GU", "GASTRIC ULCER PERFORATED", "Perforated stomach ulcer", "Ulcer;gastric;perforated", "Perforated Gastric Ulcer", "PERFORATED STOMACH ULCER", "Gastric ulcer perforated", "PERFORATED GASTRIC ULCER", "perforated gastric ulcer", "Perforated gastric ulcer", "perforation ulcer stomach", "gastric perforating ulcer", "gastric ulcer perforation", "GASTRIC ULCER PERFORATION", "Gastric ulcer perforation", "perforation; gastric ulcer", "Perforation of gastric ulcer", "GU - Perforated gastric ulcer", "Gastric ulcer with perforation", "Ulcer stomach with perforation", "Stomach ulcer with perforation", "ULCER STOMACH WITH PERFORATION", "Gastric ulcers and perforation", "ulcer; gastric, with perforation", "stomach; ulcer, with perforation", "Gastric ulcer, NOS with perforation", "Gastric ulcer with perforation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric ulcer with perforation", "shortest_name_length": 13}
{"curie": "MONDO:0009657", "names": ["MPS3C", "MPS 3C", "MPSIIIC", "MPS 3 C", "MPS IIIC", "MPS III C", "Sanfilippo C", "HGSNAT deficiency", "Sanfilippo Syndrome C", "Sanfilippo C syndrome", "Sanfilippo syndrome C", "SANFILIPPO SYNDROME C", "Sanfilippo syndrome type C", "Sanfilippo syndrome, type C", "Mucopolysaccharidosis III-C", "Mucopolysaccharidosis type 3C", "mucopolysaccharidosis type 3C", "mucopolysaccharidosis, type 3C", "Mucopolysaccharidosis Type 3 C", "Mucopoly-saccharidosis type 3C", "N-Acetyl transferase deficiency", "mucopolysaccharidosis type IIIC", "Mucopolysaccharidosis Type IIIC", "Mucopolysaccharidosis type IIIC", "MUCOPOLYSACCHARIDOSIS, TYPE IIIC", "Mucopolysaccharidosis, MPS-III-C", "mucopolysaccharidosis, type IIIC", "Mucopolysaccharidosis Type IIICs", "Mucopolysaccharidosis III-C (disorder)", "MPS III-C - Mucopolysaccharidosis III-C", "MPSIIIC - Mucopolysaccharidosis type IIIC", "mucopolysaccharidosis type IIIC (Sanfilippo C)", "Heparan-alpha-glucosaminide acetyltransferase deficiency", "heparan-alpha-glucosaminide N-acetyltransferase deficiency", "Heparan-alpha-glucosaminide N-acetyltransferase deficiency", "Acetyl-CoA alpha-glucosaminide acetyltransferase deficiency", "Acetyl-CoA:alpha-Glucosaminide N-Acetyltransferase Deficiency", "acetyl-CoA:alpha-glucosaminide N-acetyltransferase deficiency", "Acetyl CoA:alpha Glucosaminide N Acetyltransferase Deficiency", "Acetyl-CoA alpha-glucosaminide n-acetyltransferase deficiency", "ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY", "Deficiency, Acetyl-CoA:alpha-Glucosaminide N-Acetyltransferase", "N-Acetyltransferase Deficiency, Acetyl-CoA:alpha-Glucosaminide", "Acetyl-CoA:alpha-Glucosaminide N-Acetyltransferase Deficiencies", "Deficiencies, Acetyl-CoA:alpha-Glucosaminide N-Acetyltransferase", "N-Acetyltransferase Deficiencies, Acetyl-CoA:alpha-Glucosaminide", "Acetyl-CoA: heparan-alpha-D-glucosaminide N-acetyltransferase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucopolysaccharidosis type 3C", "shortest_name_length": 5}
{"curie": "MONDO:0007970", "names": ["Mel", "MEL", "Rheostosis", "LERI SYNDROME", "Melorheostosis", "MELORHEOSTOSIS", "Leri's disease", "melorheostosis", "Melorheostoses", "Candle wax disease", "MELORHEOSTOSIS LERI", "Flowing hyperostosis", "periostitis; monomelic", "Melorheostosis of Leri", "PERIOSTITIS, MONOMELIC", "monomelic; hyperostosis", "HYPEROSTOSIS, MONOMELIC", "hyperostosis; monomelic", "melorheostosis, isolated", "MELORHEOSTOSIS, ISOLATED", "Melorheostosis (disorder)", "melorheostosis (diagnosis)", "Osteopathia hyperostotica congenita", "melorheostosis, isolated, somatic mosaic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melorheostosis", "shortest_name_length": 3}
{"curie": "MONDO:0022323", "names": ["2-HEMA sensitization", "2-hydroxyethyl methacrylate sensitization", "sensitization to 2-hydroxyethyl methacrylate", "Sensitization to 2-hydroxyethyl methacrylate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "2-hydroxyethyl methacrylate sensitization", "shortest_name_length": 20}
{"curie": "UMLS:C3272815", "names": ["Colorectal Micropapillary Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Micropapillary Adenocarcinoma", "shortest_name_length": 40}
{"curie": "UMLS:C0079035", "names": ["bradyarrhythmia", "Bradyarrhythmia", "BRADYARRHYTHMIA", "bradyarrhythmias", "Bradyarrhythmia (disorder)", "bradyarrhythmia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bradyarrhythmia (disorder)", "shortest_name_length": 15}
{"curie": "UMLS:C4745077", "names": ["Treatment-sensitive HIV Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Treatment-sensitive HIV Infection", "shortest_name_length": 33}
{"curie": "UMLS:C0948086", "names": ["Intestinal mucosal hypertrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal mucosal hypertrophy", "shortest_name_length": 30}
{"curie": "MONDO:0012025", "names": ["BOS3", "BO Syndrome 3", "bo syndrome 3", "BO SYNDROME 3", "Branchiootic Syndrome 3", "BRANCHIOOTIC SYNDROME 3", "branchiootic syndrome 3", "SIX1 branchiootic syndrome", "branchiootic syndrome type 3", "BRANCHIOOTIC SYNDROME 3 (disorder)", "branchiootic syndrome caused by mutation in SIX1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "branchiootic syndrome 3", "shortest_name_length": 4}
{"curie": "UMLS:C0266328", "names": ["ectopic ureter", "Ectopic ureter", "Ectopic Ureter", "Ectopic ureters", "ectopia; ureter", "ureter; ectopia", "Ectopia of ureter", "Malposition of ureter", "Ectopic ureter (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ectopic ureter", "shortest_name_length": 14}
{"curie": "UMLS:C1517627", "names": ["Juvenile Bilateral Ovarian Granulosa Cell Tumor", "Juvenile Type Bilateral Ovarian Granulosa Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Juvenile Bilateral Ovarian Granulosa Cell Tumor", "shortest_name_length": 47}
{"curie": "UMLS:C3899401", "names": ["Decreased Visual Acuity with Current Correction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Decreased Visual Acuity with Current Correction", "shortest_name_length": 47}
{"curie": "MONDO:0029130", "names": ["PAPA8", "polydactyly, postaxial, type A8", "POLYDACTYLY, POSTAXIAL, TYPE A8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polydactyly, postaxial, type A8", "shortest_name_length": 5}
{"curie": "UMLS:C1135161", "names": ["Pepper's Syndrome", "special neuroblastoma", "Stage 4S neuroblastoma", "Stage 4S Neuroblastoma", "stage 4S neuroblastoma", "Neuroblastoma Stage IVS", "neuroblastoma, stage 4S", "Stage IVS Neuroblastoma", "stage IVS neuroblastoma", "neuroblastoma, stage IVS", "metastatic neuroblastoma", "Neuroblastoma, metastatic", "neuroblastoma, metastatic", "disseminated neuroblastoma", "neuroblastoma, disseminated", "Neuroblastoma, metastatic (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 4S neuroblastoma", "shortest_name_length": 17}
{"curie": "MONDO:0005257", "names": ["advanced heart failure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "advanced heart failure", "shortest_name_length": 22}
{"curie": "MONDO:0017280", "names": ["red mange", "Demodicosis", "demodicidosis", "demodectic mange", "Demodex infectious disease", "Demodex disease or disorder", "Demodex caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "demodicidosis", "shortest_name_length": 9}
{"curie": "UMLS:C0701821", "names": ["onychia", "ONYCHIA", "Onychia", "onyxitis", "onychitis", "onychia (diagnosis)", "Inflammation of matrix of nail", "Inflammation of matrix of nail (disorder)", "inflammatory disorder of extremity onychia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Onychia", "shortest_name_length": 7}
{"curie": "MONDO:0004053", "names": ["Bartholin Gland Squamous Cell Carcinoma", "Bartholin gland squamous cell carcinoma", "bartholin gland squamous cell carcinoma", "Bartholin's gland squamous cell carcinoma", "Bartholin's Gland Squamous Cell Carcinoma", "major vestibular gland squamous cell carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bartholin gland squamous cell carcinoma", "shortest_name_length": 39}
{"curie": "MONDO:0021661", "names": ["coronary atherosclerosis", "Coronary Atherosclerosis", "atherosclerosis of coronary artery", "coronary artery arteriosclerosis disorder", "coronary artery arteriosclerosis (disease)", "arteriosclerosis disorder of coronary artery"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coronary atherosclerosis", "shortest_name_length": 24}
{"curie": "MONDO:0034676", "names": ["overgrowth syndrome with 2q37 translocation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "overgrowth syndrome with 2q37 translocation", "shortest_name_length": 43}
{"curie": "MONDO:0014809", "names": ["MPLPF", "DDX41 hereditary neoplastic syndrome", "hereditary neoplastic syndrome caused by mutation in DDX41", "DDX41-related hematologic malignancy predisposition syndrome", "susceptibility to familial (multiple types) myeloproliferative/lymphoproliferative neoplasms", "myeloproliferative/lymphoproliferative neoplasms, familial (multiple types), susceptibility to", "MYELOPROLIFERATIVE/LYMPHOPROLIFERATIVE NEOPLASMS, FAMILIAL (MULTIPLE TYPES), SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DDX41-related hematologic malignancy predisposition syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0854992", "names": ["Stage II Squamous Cell Lung Cancer", "Stage II Squamous Cell Lung Carcinoma", "Lung Squamous Cell Carcinoma Stage II", "Lung squamous cell carcinoma stage II", "Stage II Epidermoid Cell Lung Carcinoma", "Squamous cell carcinoma of lung stage II", "Stage II Squamous Cell Carcinoma of Lung", "Stage II Epidermoid Cell Carcinoma of Lung", "Stage II Squamous Cell Carcinoma of the Lung", "Stage II Lung Squamous Cell Carcinoma AJCC v7", "Stage II Squamous Cell Lung Carcinoma AJCC v7", "Stage II Epidermoid Cell Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung squamous cell carcinoma stage II", "shortest_name_length": 34}
{"curie": "MONDO:0041448", "names": ["metastasis from malignant tumor of colon", "metastasis from malignant neoplasm of colon", "metastasis from malignant neoplasm of colon (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metastasis from malignant tumor of colon", "shortest_name_length": 40}
{"curie": "MONDO:0002578", "names": ["Botryoid sarcoma", "botryoid sarcoma", "Botryoid Sarcoma", "botryoid; sarcoma", "sarcoma; botryoid", "Sarcoma Botryoides", "sarcoma botryoides", "Sarcoma botryoides", "Botryoid rhabdomyosarcoma", "botryoid rhabdomyosarcoma", "malignant rhabdomyosarcoma botryoid", "Botryoid rhabdomyosarcoma (disorder)", "Botryoid rhabdomyosarcoma (diagnosis)", "Embryonal rhabdomyosarcoma, pleomorphic", "Botryoid-type Embryonal Rhabdomyosarcoma", "Botryoid-Type Embryonal Rhabdomyosarcoma", "botryoid-type embryonal rhabdomyosarcoma", "botryoid sarcoma (morphologic abnormality)", "Botryoid sarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "botryoid rhabdomyosarcoma", "shortest_name_length": 16}
{"curie": "MONDO:0003512", "names": ["Mediastinal Soft Tissue Tumor", "mediastinal mesenchymal tumor", "mediastinal soft tissue tumor", "mediastinal mesenchymal tumour", "soft tissue tumor of mediastinum", "mediastinal soft tissue neoplasm", "Mediastinal Soft Tissue Neoplasm", "Soft Tissue Tumor of Mediastinum", "soft tissue tumour of mediastinum", "Soft Tissue Neoplasm of Mediastinum", "soft tissue neoplasm of mediastinum", "Soft Tissue Tumor of the Mediastinum", "soft tissue tumor of the mediastinum", "soft tissue neoplasm of the mediastinum", "Soft Tissue Neoplasm of the Mediastinum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mediastinal mesenchymal tumor", "shortest_name_length": 29}
{"curie": "MONDO:0003446", "names": ["Papillary hydradenoma", "Papillary hidradenoma", "papillary hidradenoma", "Papillary Hidradenoma", "papillary; hidradenoma", "hidradenoma; papillary", "Papillary Hidradenomas", "hydradenomas papillary", "Hidradenoma, Papillary", "[M]Papillary hydradenoma", "hidradenoma papilliferum", "Hidradenoma Papilliferum", "Hidradenoma papilliferum", "Hidradenoma Papilliferums", "Papilliferum, Hidradenoma", "Tubular Sweat Gland Adenomas", "Anogenital Papillary Hidradenoma", "Papillary hidradenoma (disorder)", "Papillary Hidradenoma, Anogenital", "Anogenital Papillary Hidradenomas", "Hidradenoma, Anogenital Papillary", "Papillary hidradenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papillary hidradenoma", "shortest_name_length": 21}
{"curie": "UMLS:C4054144", "names": ["Pseudotumor of Kidney"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pseudotumor of Kidney", "shortest_name_length": 21}
{"curie": "MONDO:0016571", "names": ["Volcke-Soekarman syndrome", "Volcke Soekarman syndrome", "macrocephaly-short stature-paraplegia syndrome", "Macrocephaly-short stature-paraplegia syndrome", "Macrocephaly, short stature, paraplegia syndrome", "macrocephaly, short stature, paraplegia syndrome", "Macrocephaly, short stature, paraplegia syndrome (disorder)", "macrocephaly, short stature, paraplegia syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macrocephaly-short stature-paraplegia syndrome", "shortest_name_length": 25}
{"curie": "UMLS:C1511954", "names": ["Diffuse Leiomyomatosis Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse Leiomyomatosis Syndrome", "shortest_name_length": 31}
{"curie": "UMLS:C5206948", "names": ["Refractory Pleural Malignant Mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Pleural Malignant Mesothelioma", "shortest_name_length": 41}
{"curie": "UMLS:C1504450", "names": ["Implant site hematoma", "Implant site haematoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Implant site hematoma", "shortest_name_length": 21}
{"curie": "MONDO:0005658", "names": ["Astroviridae infection", "Astroviridae Infection", "Astroviridae Infections", "Infection, Astroviridae", "Infections, Astroviridae", "Astroviridae infectious disease", "Infection caused by Family Astroviridae", "Infection caused by Family Astroviridae (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Astroviridae infectious disease", "shortest_name_length": 22}
{"curie": "MONDO:0022173", "names": ["11q trisomy", "Trisomy 11q", "trisomy 11q", "11q syndrome", "11q+ syndrome", "11q duplication", "Duplication 11q", "dup(11q) syndrome", "partial trisomy 11q", "chromosome 11q trisomy", "Chromosome 11q trisomy", "11q duplication syndrome", "duplication 11q syndrome", "chromosome 11q duplication", "partial trisomy of chromosome 11q", "chromosome 11q duplication syndrome", "partial duplication of chromosome 11q", "partial trisomy of the long arm of chromosome 11", "partial duplication of the long arm of chromosome 11", "partial duplication of the long arm of chromosome type 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 11q trisomy", "shortest_name_length": 11}
{"curie": "UMLS:C4727424", "names": ["Recurrent Malignant Central Nervous System Neoplasm", "Recurrent Primary Malignant Central Nervous System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Primary Malignant Central Nervous System Neoplasm", "shortest_name_length": 51}
{"curie": "MONDO:0007022", "names": ["Xanthogranulomatous Pyelonephritis", "pyelonephritis xanthogranulomatous", "Xanthogranulomatous pyelonephritis", "xanthogranulomatous pyelonephritis", "Pyelonephritis, Xanthogranulomatous", "Xanthogranulomatous Pyelonephritides", "Pyelonephritides, Xanthogranulomatous", "XGP - Xanthogranulomatous pyelonephritis", "XGPN - Xanthogranulomatous pyelonephritis", "Xanthogranulomatous pyelonephritis (disorder)", "Xanthogranulomatous pyelonephritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "xanthogranulomatous pyelonephritis", "shortest_name_length": 34}
{"curie": "MONDO:0011437", "names": ["MCPH4", "primary autosomal recessive microcephaly 4", "microcephaly 4, primary, autosomal recessive", "Microcephaly, Primary Autosomal Recessive, 4", "MICROCEPHALY 4, PRIMARY, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly 4, primary, autosomal recessive", "shortest_name_length": 5}
{"curie": "UMLS:C1321781", "names": ["Malignant chondroid syringoma", "malignant mixed tumor of skin", "Malignant Chondroid Syringoma", "Eccrine mixed tumor, malignant", "Cutaneous Malignant Mixed Tumor", "Eccrine mixed tumour, malignant", "Malignant Mixed Tumor of the Skin", "Malignant mixed tumor of the skin", "Malignant mixed tumour of the skin", "Malignant chondroid syringoma of skin", "malignant mixed tumor of skin (diagnosis)", "Malignant chondroid syringoma of skin (disorder)", "Malignant chondroid syringoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant chondroid syringoma", "shortest_name_length": 29}
{"curie": "UMLS:C4288303", "names": ["Recurrent Solid Tumor", "Relapsed Solid Neoplasm", "Recurrent Solid Neoplasm", "Recurrent Malignant Solid Tumor", "Relapsed Malignant Solid Neoplasm", "Recurrent Malignant Solid Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Malignant Solid Neoplasm", "shortest_name_length": 21}
{"curie": "MONDO:0013198", "names": ["CMD1EE", "dilated cardiomyopathy 1EE", "Cardiomyopathy, Dilated, 1EE", "cardiomyopathy, dilated, 1EE", "CARDIOMYOPATHY, DILATED, 1EE", "dilated cardiomyopathy type 1EE", "cardiomyopathy, dilated, type 1Ee", "MYH6 familial isolated dilated cardiomyopathy", "familial isolated dilated cardiomyopathy caused by mutation in MYH6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1EE", "shortest_name_length": 6}
{"curie": "UMLS:C4054912", "names": ["Fusion-Positive Alveolar Rhabdomyosarcoma", "Fusion Gene Positive Alveolar Rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fusion-Positive Alveolar Rhabdomyosarcoma", "shortest_name_length": 41}
{"curie": "MONDO:0018882", "names": ["angiitis", "Angiitis", "ANGIITIS", "vasculitis", "Angiitides", "VASCULITIS", "Vasculitis", "vasculitides", "Vasculitides", "Angiitis, NOS", "Vasculitis NOS", "Vasculitis, NOS", "systemic vasculitis", "Systemic vasculitis", "vasculitis; syndrome", "syndrome; vasculitis", "Vasculitis (disorder)", "vasculitis (diagnosis)", "VASCULITIS NON SPECIFIC", "Vasculitis, nonspecific", "Inflammation of blood vessel", "infection of the blood vessel", "vascular inflammation or infection", "infection of the blood or lymph vessel"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vasculitis", "shortest_name_length": 8}
{"curie": "UMLS:C1370943", "names": ["Recurrent Optic Nerve Glioma", "Recurrent Pediatric Optic Nerve Glioma", "recurrent childhood optic nerve glioma", "Recurrent Childhood Optic Nerve Glioma", "childhood recurrent optic nerve glioma", "pediatric recurrent optic nerve glioma", "recurrent glioma, pediatric optic nerve", "recurrent glioma, childhood optic nerve", "recurrent optic nerve glioma, childhood", "glioma, pediatric optic nerve, recurrent", "optic nerve glioma, childhood, recurrent", "optic nerve glioma, pediatric, recurrent", "glioma, childhood optic nerve, recurrent", "recurrent childhood CNS tumor, optic nerve glioma", "recurrent pediatric CNS tumor, optic nerve glioma", "childhood CNS tumor, recurrent optic nerve glioma", "pediatric CNS tumor, optic nerve glioma, recurrent", "recurrent childhood brain tumor, optic nerve glioma", "recurrent pediatric brain tumor, optic nerve glioma", "childhood brain tumor, recurrent optic nerve glioma", "pediatric brain tumor, optic nerve glioma, recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Optic Nerve Glioma", "shortest_name_length": 28}
{"curie": "UMLS:C0236993", "names": ["Other sleep disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Other sleep disorders", "shortest_name_length": 21}
{"curie": "MONDO:0006743", "names": ["endocrine tuberculosis", "Endocrine Tuberculosis", "Endocrine Tuberculoses", "Tuberculoses, Endocrine", "Tuberculosis, Endocrine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endocrine tuberculosis", "shortest_name_length": 22}
{"curie": "UMLS:C0280157", "names": ["stage III grade 2 follicular lymphoma", "Stage III Grade 2 Follicular Lymphoma", "Grade II Follicular Lymphoma Stage III", "Stage III Grade II Follicular Lymphoma", "stage III follicular mixed cell lymphoma", "Follicular Mixed Cell Lymphoma Stage III", "Stage III Follicular Mixed Cell Lymphoma", "follicular mixed cell lymphoma, stage III", "Ann Arbor Stage III Grade 2 Follicular Lymphoma", "Stage III Grade II Follicular Mixed Cell Lymphoma", "Grade II Follicular Mixed Cell Lymphoma Stage III", "stage III grade II follicular mixed cell lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage III Grade 2 Follicular Lymphoma", "shortest_name_length": 37}
{"curie": "MONDO:0032910", "names": ["MC1DN34", "nuclear type mitochondrial complex I deficiency 34", "mitochondrial complex 1 deficiency, nuclear type 34", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 34"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 34", "shortest_name_length": 7}
{"curie": "UMLS:C1707736", "names": ["First use syndrome", "Dialyzer First Use Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "First use syndrome", "shortest_name_length": 18}
{"curie": "MONDO:0015523", "names": ["Epithelioid Angiosarcoma", "epithelioid angiosarcoma", "epithelioid angioendothelioma", "Epithelioid Angioendothelioma", "epithelioid hemangioendothelioma", "Epithelioid hemangioendothelioma", "Epithelioid Hemangioendothelioma", "Hemangioendothelioma, Epithelioid", "Epithelioid haemangioendothelioma", "Epithelioid Hemangioendotheliomas", "Hemangioendotheliomas, Epithelioid", "Epithelioid hemangioendothelioma NOS", "Epithelioid hemangioendothelioma, NOS", "Epithelioid haemangioendothelioma NOS", "Epithelioid haemangioendothelioma, NOS", "Malignant epithelioid hemangioendothelioma", "malignant epithelioid hemangioendothelioma", "Epithelioid hemangioendothelioma, malignant", "Malignant epithelioid haemangioendothelioma", "Epithelioid hemangioendothelioma (disorder)", "epithelioid hemangioendothelioma (diagnosis)", "Epithelioid haemangioendothelioma, malignant", "[M] Epithelioid hemangioendothelioma, malignant", "[M] Epithelioid haemangioendothelioma, malignant", "malignant epithelioid hemangioendothelioma (diagnosis)", "neoplasm - soft tissue blood vessel hemangioendothelioma epithelioid", "Epithelioid hemangioendothelioma, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epithelioid hemangioendothelioma", "shortest_name_length": 24}
{"curie": "MONDO:0004746", "names": ["Extraocular myopathy", "extraocular myopathy", "extra-ocular muscle myopathy", "extraocular muscles; myopathy", "myopathy; extraocular muscles", "myopathy of extraocular muscle", "myopathy of extraocular muscles", "Myopathy of extraocular muscles", "myopathy of extra-ocular muscle", "extraocular myopathy (diagnosis)", "Myopathy of extraocular muscles (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy of extraocular muscle", "shortest_name_length": 20}
{"curie": "UMLS:C0349541", "names": ["Brain Malignant Glioma", "Malignant Brain Glioma", "High Grade Brain Glioma", "High-Grade Brain Glioma", "Brain High-Grade Glioma", "Brain High Grade Glioma", "malignant glioma of brain", "Malignant glioma of brain", "Malignant glioma of brain (disorder)", "malignant glioma of brain (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant glioma of brain", "shortest_name_length": 22}
{"curie": "MONDO:0000151", "names": ["symphalangism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "symphalangism", "shortest_name_length": 13}
{"curie": "MONDO:0011138", "names": ["SLEB1", "systemic lupus erythematosus, resistance to", "TLR5 systemic lupus erythematosus (disease)", "systemic lupus erythematosus, resistance to, 1", "SYSTEMIC LUPUS ERYTHEMATOSUS, RESISTANCE TO, 1", "susceptibility to systemic lupus erythematosus 1", "systemic lupus erythematosus, susceptibility to, 1", "SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 1", "systemic lupus erythematosus, susceptibility to, type 1", "systemic lupus erythematosus (disease) caused by mutation in TLR5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "systemic lupus erythematosus, susceptibility to, 1", "shortest_name_length": 5}
{"curie": "MONDO:0032723", "names": ["BRIDA", "IMD60", "IMMUNODEFICIENCY 60", "immunodeficiency 60", "immunodeficiency 60 and autoimmunity", "IMMUNODEFICIENCY 60 AND AUTOIMMUNITY", "BACH2-related immunodeficiency and autoimmunity", "Immunodeficiency and Autoimmunity, Bach2-Related", "IMMUNODEFICIENCY AND AUTOIMMUNITY, BACH2-RELATED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 60", "shortest_name_length": 5}
{"curie": "MONDO:0002476", "names": ["ANURIA", "anuria", "Anuria", "anurias", "Anurias", "Passes no urine", "Anuria (finding)", "Absent urine output", "Urine volume, absence", "Absence of urine volume", "URINARY OUTPUT ARREST OF", "Urinary output arrest of", "Arrest of urinary output", "Urine formation failure of", "URINE FORMATION FAILURE OF", "Failure of urine formation", "suppression; urinary secretion", "secretion; urinary, suppression", "urinary; secretion, suppression", "Suppression of urinary secretion", "suppression of urinary secretion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anuria", "shortest_name_length": 6}
{"curie": "MONDO:0030928", "names": ["MCPH26", "MICROCEPHALY 26, PRIMARY, AUTOSOMAL DOMINANT", "microcephaly 26, primary, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly 26, primary, autosomal dominant", "shortest_name_length": 6}
{"curie": "MONDO:0014650", "names": ["ETL8", "familial temporal lobe epilepsy 8", "epilepsy, familial temporal lobe, 8", "EPILEPSY, FAMILIAL TEMPORAL LOBE, 8", "familial temporal lobe epilepsy type 8", "epilepsy, familial temporal lobe, type 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial temporal lobe epilepsy 8", "shortest_name_length": 4}
{"curie": "UMLS:C1516067", "names": ["Astler-Coller B3 Rectal Carcinoma", "Astler-Coller B3 Carcinoma of Rectum", "Astler-Coller B3 Carcinoma of the Rectum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Astler-Coller B3 Rectal Carcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C2981259", "names": ["Stage IVC Mucosal Melanoma of the Head and Neck", "Stage IVC Mucosal Melanoma of the Head and Neck AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Mucosal Melanoma of the Head and Neck AJCC v7", "shortest_name_length": 47}
{"curie": "MONDO:0009010", "names": ["aortic arch interruption"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic arch interruption", "shortest_name_length": 24}
{"curie": "UMLS:C4725596", "names": ["Cervical Esophagus Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Esophagus Adenocarcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C5417749", "names": ["IGBC", "Occult Gallbladder Cancer", "Occult Gallbladder Carcinoma", "Incidental Gallbladder Cancer", "Incidental Gallbladder Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Incidental Gallbladder Carcinoma", "shortest_name_length": 4}
{"curie": "UMLS:C0015376", "names": ["leakage", "Leakage", "Spillage", "spillage", "spillages", "Leakage, NOS", "extravasation", "Spillage, NOS", "Extravasation", "EXTRAVASATION", "Extravasations", "EXTRAVASATIONS", "extravasations", "Extravasation NOS", "Extravasation, NOS", "Extravasation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extravasation", "shortest_name_length": 7}
{"curie": "MONDO:0100070", "names": ["neuroendocrine disorder", "neuroendocrine system disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuroendocrine disorder", "shortest_name_length": 23}
{"curie": "UMLS:C5419771", "names": ["Gastric Neuroendocrine Tumor G3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Neuroendocrine Tumor G3", "shortest_name_length": 31}
{"curie": "UMLS:C0027535", "names": ["Neck sprain", "sprain neck", "neck sprain", "Neck Sprain", "Sprain;neck", "neck sprains", "sprained neck", "neck sprained", "necks sprained", "sprain of neck", "Sprain of neck", "of neck sprain", "Cervical sprain", "cervical sprain", "Sprain of neck, NOS", "Acute cervical sprain", "Neck sprain (disorder)", "sprain of neck (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neck sprain", "shortest_name_length": 11}
{"curie": "MONDO:0011939", "names": ["SEM", "SPENCD", "SPENCDI", "Roifman-Costa syndrome", "Roifman-Melamed syndrome", "spondyloenchondromatosis", "spondyloenchondrodysplasia", "ROIFMAN IMMUNOSKELETAL SYNDROME", "Roifman Immunoskeletal syndrome", "SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION", "spondyloenchondrodysplasia with immune dysregulation", "Spondyloenchondrodysplasia with immune dysregulation", "Spondyloenchondrodysplasia with Immune Dysregulation", "spondylometaphyseal dysplasia with enchondromatous changes", "spondylometaphyseal dysplasia with combined immunodeficiency", "Spondyloenchondrodysplasia with immune dysregulation (disorder)", "Combined Immunodeficiency with Autoimmunity and Spondylometaphyseal Dysplasia", "combined immunodeficiency with autoimmunity and spondylometaphyseal dysplasia", "Combined immunodeficiency with autoimmunity and spondylometaphyseal dysplasia", "COMBINED IMMUNODEFICIENCY WITH AUTOIMMUNITY AND SPONDYLOMETAPHYSEAL DYSPLASIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spondyloenchondrodysplasia with immune dysregulation", "shortest_name_length": 3}
{"curie": "UMLS:C0340496", "names": ["Congenital complete AV block", "Congenital Complete AV Block", "Congenital Third Degree Block", "Congenital complete heart block", "Congenital Complete Atrioventricular Block", "Congenital complete atrioventricular block", "Complete atrioventricular block, congenital", "Congenital complete atrioventricular heart block", "Congenital complete atrioventricular heart block (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital complete heart block", "shortest_name_length": 28}
{"curie": "UMLS:C0863111", "names": ["Nasal mucus blood tinged"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasal mucus blood tinged", "shortest_name_length": 24}
{"curie": "MONDO:0012515", "names": ["GLC1M", "JOAG1M", "glaucoma 1, open angle, M", "GLAUCOMA 1, OPEN ANGLE, M", "Glaucoma 1, Open Angle, M"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glaucoma 1, open angle, M", "shortest_name_length": 5}
{"curie": "MONDO:0012091", "names": ["HIIMS", "DFNB32", "DFNB105", "DFNB105, FORMERLY", "autosomal recessive deafness 32", "deafness, autosomal recessive 32", "Deafness, Autosomal Recessive 32", "DEAFNESS, AUTOSOMAL RECESSIVE 32", "autosomal recessive deafness 105", "deafness, autosomal recessive 105", "deafness, autosomal recessive type 105", "hearing impairment infertile male syndrome", "HEARING IMPAIRMENT INFERTILE MALE SYNDROME", "DEAFNESS, AUTOSOMAL RECESSIVE 105, FORMERLY", "autosomal recessive nonsyndromic deafness 32", "autosomal recessive nonsyndromic deafness 105", "CDC14A autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 32", "autosomal recessive nonsyndromic deafness type 32", "autosomal recessive nonsyndromic deafness type 105", "deafness, autosomal recessive 32, with or without immotile sperm", "DEAFNESS, AUTOSOMAL RECESSIVE 32, WITH OR WITHOUT IMMOTILE SPERM", "autosomal recessive nonsyndromic deafness caused by mutation in CDC14A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 32", "shortest_name_length": 5}
{"curie": "MONDO:0007008", "names": ["uremia", "UREMIA", "Uremia", "URAEMIA", "uraemia", "Uraemia", "Uremias", "Uremia NOS", "Uremia, NOS", "Uraemia, NOS", "Uremia (disorder)", "uremia (diagnosis)", "urea in blood; high", "UREMIA OF renal ORIGIN", "Uremia of renal origin", "UREMIA OF RENAL ORIGIN", "uremia of renal origin", "URAEMIA OF RENAL ORIGIN", "Uraemia of renal origin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uremia", "shortest_name_length": 6}
{"curie": "UMLS:C2828253", "names": ["Stage IVC Lip and Oral Cavity Cancer", "stage IVC lip and oral cavity cancer", "Stage IVC Lip and Oral Cavity Cancer AJCC v7", "Stage IVC Lip and Oral Cavity Cancer AJCC v6", "Stage IVC Lip and Oral Cavity Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Lip and Oral Cavity Cancer AJCC v6 and v7", "shortest_name_length": 36}
{"curie": "MONDO:0020831", "names": ["VCRL", "vertebral, cardiac, renal, and limb defects syndrome", "congenital vertebral-cardiac-renal anomalies syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital vertebral-cardiac-renal anomalies syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0014212", "names": ["MOCODC", "MOCOD type C", "molybdenum cofactor deficiency C", "molybdenum cofactor deficiency type C", "Molybdenum Cofactor Deficiency Type C", "Molybdenum cofactor deficiency complementation group C", "molybdenum cofactor deficiency complementation group C", "Molybdenum Cofactor Deficiency, Complementation Group C", "molybdenum cofactor deficiency, complementation group C", "MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP C", "molybdenum cofactor deficiency, complementation group type C", "Molybdenum cofactor deficiency complementation group C (disorder)", "sulfite oxidase deficiency due to molybdenum cofactor deficiency type C", "Sulfite oxidase deficiency due to molybdenum cofactor deficiency type C", "Combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type C", "combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type C"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sulfite oxidase deficiency due to molybdenum cofactor deficiency type C", "shortest_name_length": 6}
{"curie": "UMLS:C4524726", "names": ["Pathologic Stage IA Gastroesophageal Junction Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IA Gastroesophageal Junction Adenocarcinoma AJCC v8", "shortest_name_length": 68}
{"curie": "UMLS:C1266109", "names": ["Large cell calcifying Sertoli cell tumor", "Large cell calcifying Sertoli cell tumour", "Testicular Large Cell Calcifying Sertoli Cell Tumor", "Large cell calcifying Sertoli cell tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Large cell calcifying Sertoli cell tumor", "shortest_name_length": 40}
{"curie": "MONDO:0000626", "names": ["vestibular gland benign neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vestibular gland benign neoplasm", "shortest_name_length": 32}
{"curie": "MONDO:0009858", "names": ["PPT syndrome", "PPT SYNDROME", "Pfeiffer-Palm-Teller Syndrome", "Pfeiffer-Palm-Teller syndrome", "Pfeiffer Palm Teller syndrome", "PFEIFFER-PALM-TELLER SYNDROME", "PPT (Pfeiffer Palm Teller) syndrome", "short stature unique facies enamel hypoplasia progressive joint stiffness and high-pitched voice", "short stature, unique facies, enamel hypoplasia, progressive Joint stiffness, and high-pitched voice", "SHORT STATURE, UNIQUE FACIES, ENAMEL HYPOPLASIA, PROGRESSIVE JOINT STIFFNESS, AND HIGH-PITCHED VOICE", "Short stature, unique facies, enamel hypoplasia, progressive joint stiffness, high-pitched voice syndrome", "Short stature, unique facies, enamel hypoplasia, progressive joint stiffness, high-pitched voice syndrome (disorder)", "Short stature, unique facies, enamel hypoplasia, progressive joint stiffness, high-pitched voice syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pfeiffer-Palm-Teller syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0013173", "names": ["MRT13", "Mrt13", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 13", "mental retardation, autosomal recessive 13", "Mental Retardation, Autosomal Recessive 13", "intellectual disability, autosomal recessive 13", "mental retardation, autosomal recessive type 13", "intellectual disability, autosomal recessive type 13", "autosomal recessive intellectual developmental disorder 13", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 13", "TRAPPC9 autosomal recessive non-syndromic intellectual disability", "autosomal recessive non-syndromic intellectual disability caused by mutation in TRAPPC9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 13", "shortest_name_length": 5}
{"curie": "UMLS:C1699326", "names": ["Vas deferens anastomotic leak", "anastomotic leak vas deferens", "anastomotic leak of vas deferens", "Vas Deferens Anastomotic Leakage", "anastomotic leak of vas deferens (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vas Deferens Anastomotic Leakage", "shortest_name_length": 29}
{"curie": "UMLS:C5419778", "names": ["Duodenal Neuroendocrine Tumor G3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Duodenal Neuroendocrine Tumor G3", "shortest_name_length": 32}
{"curie": "UMLS:C2018776", "names": ["Splenic Lymphoplasmacytic Lymphoma", "lymphoplasmacytic lymphoma of spleen", "lymphoplasmacytic lymphoma of spleen (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Splenic Lymphoplasmacytic Lymphoma", "shortest_name_length": 34}
{"curie": "UMLS:C0422855", "names": ["Epileptic vertigo", "epileptic vertigo", "Vertigo, epileptic", "Vestibular Seizure", "epileptic; vertigo", "vertigo; epileptic", "Seizure, Vestibular", "Vestibular Seizures", "vestibular seizures", "Vertiginous Seizure", "Vertiginous seizure", "vertiginous epilepsy", "Vertiginous epilepsy", "Seizure, Vertiginous", "Seizures, Vestibular", "Vertiginous Seizures", "Seizures, Vertiginous", "Epileptic vertigo (disorder)", "epileptic vertigo (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vertiginous seizure", "shortest_name_length": 17}
{"curie": "MONDO:0019319", "names": ["Verrucous nevus", "Verrucous Nevus", "verrucous nevus", "Nevus, Verrucous", "verrucous; nevus", "Epithelial nevus", "verrucous naevus", "nevus verrucosus", "Verrucous naevus", "Nevus verrucosus", "nevus; verrucous", "Naevus verrucosus", "Epithelial naevus", "verrucous Epidermal Nevus", "Verrucous epidermal nevus", "Verrucous Epidermal Nevus", "Verrucous epidermal naevus", "Verrucous epidermal nevus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "verrucous nevus", "shortest_name_length": 15}
{"curie": "MONDO:0006378", "names": ["pleural epithelioid mesothelioma", "Pleural Epithelioid Mesothelioma", "pleura malignant epithelioid mesothelioma", "malignant epithelioid mesothelioma of pleura"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pleural epithelioid mesothelioma", "shortest_name_length": 32}
{"curie": "UMLS:C0855154", "names": ["Primary mediastinal large B-cell lymphoma refractory", "Refractory Primary Mediastinal Large B-Cell Lymphoma", "Refractory Mediastinal (Thymic) Large B-Cell Lymphoma", "Refractory Primary Mediastinal (Thymic) Large B-Cell Lymphoma", "Large B-cell lymphoma subtype primary mediastinal (Thymic) large B-cell lymphoma refractory"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary mediastinal large B-cell lymphoma refractory", "shortest_name_length": 52}
{"curie": "UMLS:C0032796", "names": ["Postpartum Amenorrhea", "Amenorrhea, Postpartum", "Postpartum Amenorrheas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postpartum Amenorrhea", "shortest_name_length": 21}
{"curie": "UMLS:C0877398", "names": ["Anemia postoperative", "Anaemia postoperative"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anemia postoperative", "shortest_name_length": 20}
{"curie": "MONDO:0011802", "names": ["HCA1", "Hca1", "hypercalciuria, absorptive", "hypercalciuria, absorptive, 1", "Hypercalciuria, Absorptive, 1", "HYPERCALCIURIA, ABSORPTIVE, 1", "hypercalciuria, absorptive, type 1", "HYPERCALCIURIA, ABSORPTIVE, 1 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypercalciuria, absorptive, 1", "shortest_name_length": 4}
{"curie": "MONDO:0004304", "names": ["Parathyroid mixed cell type adenoma", "Parathyroid Mixed Cell Type Adenoma", "parathyroid mixed cell type adenoma", "mixed cell type adenoma, parathyroid", "mixed cell type adenoma of parathyroid", "Mixed Cell Type Adenoma of Parathyroid", "Parathyroid Gland Mixed Cell Type Adenoma", "parathyroid gland mixed cell type adenoma", "mixed cell type adenoma of the parathyroid", "Mixed Cell Type Adenoma of the Parathyroid", "Mixed Cell Type Adenoma of Parathyroid Gland", "mixed cell type adenoma of parathyroid gland", "Mixed Cell Type Adenoma of the Parathyroid Gland", "mixed cell type adenoma of the Parathyroid gland", "mixed cell type adenoma of the parathyroid gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed cell type adenoma of parathyroid", "shortest_name_length": 35}
{"curie": "MONDO:0003120", "names": ["mixed germ cell tumor", "testis mixed germ cell tumor", "Mixed Germ Cell Tumor of Testis", "mixed germ cell tumor of testis", "Testicular Mixed Germ Cell Tumor", "Testicular germ cell tumor mixed", "mixed germ cell tumour of testis", "testicular mixed germ cell tumor", "mixed testicular germ cell tumor", "mixed testicular germ cell tumour", "Testicular germ cell tumour mixed", "mixed testicular germ cell cancer", "testicular germ cell tumor (mixed)", "Testicular Germ Cell Tumor (Mixed)", "Mixed Germ Cell Neoplasm of Testis", "mixed germ cell neoplasm of testis", "mixed germ cell tumor of the testis", "Mixed Germ Cell Tumor of the Testis", "Testicular Mixed Germ Cell Neoplasm", "testicular mixed germ cell neoplasm", "mixed germ cell neoplasm of the testis", "Mixed Germ Cell Neoplasm of the Testis", "malignant mixed germ cell tumor of testis", "malignant mixed germ cell tumor of testis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed testicular germ cell cancer", "shortest_name_length": 21}
{"curie": "UMLS:C0751797", "names": ["Traumatic Intracranial Hematoma", "Traumatic intracranial hematoma", "Traumatic Intracranial Hematomas", "Intracranial Hematoma, Traumatic", "Traumatic intracranial haematoma", "Hematoma, Traumatic Intracranial", "Intracranial Hematomas, Traumatic", "Hematomas, Traumatic Intracranial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intracranial Hematoma, Traumatic", "shortest_name_length": 31}
{"curie": "UMLS:C0854890", "names": ["Localized Pleural Malignant Mesothelioma", "Pleural mesothelioma malignant localised", "Pleural mesothelioma malignant localized"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pleural mesothelioma malignant localised", "shortest_name_length": 40}
{"curie": "MONDO:0009575", "names": ["TRMA", "THMD1", "roger syndrome", "rogers syndrome", "ROGERS SYNDROME", "Abboud syndrome", "Rogers syndrome", "thiamine-responsive myelodysplasia", "THIAMINE-RESPONSIVE MYELODYSPLASIA", "Thiamine-Responsive Myelodysplasia", "Thiamine responsive myelodysplasia", "thiamine-responsive Anemia syndrome", "thiamine-responsive anemia syndrome", "Thiamine-Responsive Anemia Syndrome", "THIAMINE-RESPONSIVE ANEMIA SYNDROME", "thiamine-responsive anaemia syndrome", "thiamine metabolism dysfunction syndrome 1", "thiamine-responsive megaloblastic anemia syndrome", "THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME", "Thiamine responsive megaloblastic anemia syndrome", "Thiamine-responsive megaloblastic anemia syndrome", "Thiamine-Responsive Megaloblastic Anemia Syndrome", "thiamine responsive megaloblastic anemia syndrome", "thiamine-responsive megaloblastic anaemia syndrome", "Thiamine-responsive megaloblastic anaemia syndrome", "thiamine-responsive megaloblastic anemia with diabetes mellitus and sensorineural deafness", "Thiamine-responsive megaloblastic anemia with diabetes mellitus and sensorineural deafness", "megaloblastic anemia thiamine-responsive with diabetes mellitus and sensorineural deafness", "thiamine-responsive megaloblastic anaemia with diabetes mellitus and sensorineural deafness", "Megaloblastic Anemia, Thiamine-Responsive, With Diabetes Mellitus And Sensorineural Deafness", "Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness", "MEGALOBLASTIC ANEMIA, THIAMINE-RESPONSIVE, WITH DIABETES MELLITUS AND SENSORINEURAL DEAFNESS", "megaloblastic Anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness", "Megaloblastic anaemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness", "Thiamine-responsive megaloblastic anemia with diabetes mellitus and sensorineural hearing loss", "thiamine metabolism dysfunction syndrome 1 (megaloblastic anemia, diabetes mellitus and deafness type)", "thiamine metabolism dysfunction syndrome 1 (megaloblastic Anemia, diabetes mellitus, and deafness type)", "Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness (disorder)", "THIAMINE METABOLISM DYSFUNCTION SYNDROME 1 (MEGALOBLASTIC ANEMIA, DIABETES MELLITUS, AND DEAFNESS TYPE)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thiamine-responsive megaloblastic anemia syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0001621", "names": ["Tick-Borne Relapsing Fever", "tick-borne relapsing fever", "Tick-borne relapsing fever", "Relapsing fever, tick-borne", "tick-borne; relapsing fever", "Tick-borne relapsing fever, NOS", "Tick-borne relapsing fever (disorder)", "tick-borne relapsing fever (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tick-borne relapsing fever", "shortest_name_length": 26}
{"curie": "UMLS:C0232808", "names": ["SHUTDOWN RENAL", "Shutdown renal", "renal shutdown", "Absent renal function", "nonfunctioning kidney", "Nonfunctioning kidney", "Non-functioning kidney", "Renal function, absent", "nonfunctioning; kidney", "non-functioning kidney", "kidney; nonfunctioning", "NFK - Non-functioning kidney", "Absent renal function (disorder)", "Non-functioning kidney (disorder)", "nonfunctioning kidney (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Absent renal function", "shortest_name_length": 14}
{"curie": "MONDO:0030858", "names": ["IMD75", "immunodeficiency 75", "IMMUNODEFICIENCY 75"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 75", "shortest_name_length": 5}
{"curie": "MONDO:0004712", "names": ["Herpes", "herpeticum eczema", "Eczema Herpeticum", "Eczema herpeticum", "eczema herpeticum", "herpeticum; eczema", "eczema; herpeticum", "Simplexvirus dermatitis", "Herpesviral blepharitis", "Herpes Simplex Dermatitis", "Herpes simplex dermatitis", "dermatitis herpes simplex", "herpes simplex dermatitis", "Eczema herpeticum (disorder)", "Kaposi Varicelliform Eruption", "eczema herpeticum (diagnosis)", "KAPOSI VARICELLIFORM ERUPTION", "Simplexvirus caused dermatitis", "Varicelliform Eruption, Kaposi", "Eruption, Kaposi Varicelliform", "Kaposis Varicelliform Eruption", "varicelliform eruption; Kaposi", "Kaposi; varicelliform eruption", "Kaposi's varicelliform eruption", "Kaposi's Varicelliform Eruption", "Herpes simplex virus dermatitis", "Eruption, Kaposi's Varicelliform", "Varicelliform Eruption, Kaposi's", "Herpes simplex eyelid dermatitis", "eruption; varicelliform, Kaposi's", "varicelliform, Kaposi's; eruption", "Herpes simplex dermatitis of eyelid", "herpes simplex virus eyelid dermatitis", "eczema herpeticum (disorder) [ambiguous]", "Herpes simplex eyelid dermatitis (disorder)", "skin; eruption, Kaposi, kaposi's varicelliform", "eruption; skin, Kaposi, kaposi's varicelliform", "Herpes simplex dermatitis of eyelid (diagnosis)", "Eczema herpeticum - Kaposi's varicelliform eruption"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "herpes simplex dermatitis", "shortest_name_length": 6}
{"curie": "UMLS:C2825578", "names": ["Transferase Deficient Galactosemia", "Transferase-deficient Galactosemia", "Transferase Deficiency Galactosemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transferase Deficiency Galactosemia", "shortest_name_length": 34}
{"curie": "UMLS:C5557678", "names": ["Uterine Ligament Adenomyoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Ligament Adenomyoma", "shortest_name_length": 27}
{"curie": "MONDO:0012423", "names": ["MORMS", "MORM SYNDROME", "MORM syndrome", "mental retardation, truncal obesity, retinal dystrophy and micropenis", "Mental retardation, truncal Obesity, Retinal dystrophy and Micropenis", "mental retardation, truncal obesity, retinal dystrophy, and micropenis", "Mental Retardation, Truncal Obesity, Retinal Dystrophy, And Micropenis", "mental retardation-truncal obesity-retinal dystrophy-micropenis syndrome", "intellectual disability, truncal obesity, retinal dystrophy and micropenis", "Intellectual disability-truncal obesity-retinal dystrophy-micropenis syndrome", "intellectual disability-truncal obesity-retinal dystrophy-micropenis syndrome", "Mental retardation, truncal obesity, retinal dystrophy and micropenis syndrome", "mental retardation, truncal obesity, retinal dystrophy, and micropenis syndrome", "MENTAL RETARDATION, TRUNCAL OBESITY, RETINAL DYSTROPHY, AND MICROPENIS SYNDROME", "MORM (mental retardation, truncal obesity, retinal dystrophy, micropenis) syndrome", "Intellectual disability, truncal obesity, retinal dystrophy and micropenis syndrome", "intellectual disability, truncal obesity, retinal dystrophy, and micropenis syndrome", "Intellectual disability, truncal obesity, retinal dystrophy and micropenis syndrome (disorder)", "IMPAIRED INTELLECTUAL DEVELOPMENT, TRUNCAL OBESITY, RETINAL DYSTROPHY, AND MICROPENIS SYNDROME", "Intellectual disability, truncal obesity, retinal dystrophy and micropenis syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MORM syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0032631", "names": ["MC1DN27", "nuclear type mitochondrial complex I deficiency 27", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 27", "mitochondrial complex 1 deficiency, nuclear type 27"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 27", "shortest_name_length": 7}
{"curie": "MONDO:0033570", "names": ["COXPD50", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 50", "combined oxidative phosphorylation deficiency 50"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation deficiency 50", "shortest_name_length": 7}
{"curie": "MONDO:0004709", "names": ["occipital lobe tumor", "Occipital Lobe Tumor", "Occipital Lobe Neoplasm", "Tumor of Occipital Lobe", "occipital lobe neoplasm", "tumor of occipital lobe", "tumor of Occipital Lobe", "Neoplasm of Occipital Lobe", "Neoplasm of occipital lobe", "neoplasm of occipital lobe", "Tumor of the Occipital Lobe", "tumor of the occipital lobe", "neoplasm of the occipital lobe", "Neoplasm of the Occipital Lobe", "occipital lobe neoplasm (disease)", "neoplasm of occipital lobe of brain", "malignant neoplasm of occipital lobe", "Malignant neoplasm of occipital lobe", "Neoplasm of occipital lobe (disorder)", "Malignant neoplasm of occipital lobe (disorder)", "neoplasm of occipital lobe of brain (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "occipital lobe neoplasm", "shortest_name_length": 20}
{"curie": "UMLS:C0026141", "names": ["Burnett", "Burnett syndrome", "BURNETT SYNDROME", "burnett syndrome", "Burnett's syndrome", "burnett's syndrome", "Milk-alkali syndrome", "milk-alkali syndrome", "MILK-ALKALI SYNDROME", "Milk-Alkali Syndrome", "milk alkali syndrome", "Milk Alkali Syndrome", "Milk alkali syndrome", "Syndrome, Milk-Alkali", "MILK DRINKER SYNDROME", "syndrome; milk-alkali", "milk-alkali; syndrome", "drinkers milk syndrome", "Milk alkali syndrome (disorder)", "milk alkali syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Milk-Alkali Syndrome", "shortest_name_length": 7}
{"curie": "UMLS:C5420233", "names": ["Oral Mucosa Langerhans Cell Histiocytosis", "Oral Cavity Langerhans Cell Histiocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral Mucosa Langerhans Cell Histiocytosis", "shortest_name_length": 41}
{"curie": "UMLS:C0152154", "names": ["Long labor", "labor long", "long labor", "labors long", "Long labour", "prolonged labor", "Labor prolonged", "LABOR PROLONGED", "Prolonged labor", "Long labor, NOS", "prolonged; labor", "Long labour, NOS", "Labor, prolonged", "prolonged labour", "Prolonged labour", "labor; prolonged", "Prolonged labor NOS", "Prolonged labor, NOS", "Prolonged labour, NOS", "Long labor, unspecified", "Long labour, unspecified", "Poor progression in labor", "Poor progression of labor", "Poor progression of labour", "Prolonged labor (disorder)", "prolonged labor (diagnosis)", "Prolonged labor, unspecified", "Prolonged labour, unspecified", "labor; prolonged or protracted"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prolonged labor", "shortest_name_length": 10}
{"curie": "UMLS:C4524093", "names": ["Euglycemic diabetic ketoacidosis", "Euglycaemic diabetic ketoacidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Euglycaemic diabetic ketoacidosis", "shortest_name_length": 32}
{"curie": "MONDO:0003075", "names": ["bilateral retinoblastoma", "Retinoblastoma bilateral", "Bilateral Retinoblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bilateral retinoblastoma", "shortest_name_length": 24}
{"curie": "MONDO:0012982", "names": ["EA6", "episodic ataxia type 6", "Episodic ataxia type 6", "episodic ataxia, type 6", "EPISODIC ATAXIA, TYPE 6", "Episodic Ataxia, Type 6", "SLC1A3 hereditary episodic ataxia", "Episodic ataxia type 6 (disorder)", "hereditary episodic ataxia caused by mutation in SLC1A3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "episodic ataxia type 6", "shortest_name_length": 3}
{"curie": "MONDO:0012923", "names": ["CGL3", "Cgl3", "BSCL3", "Bscl3", "congenital generalized lipodystrophy type 3", "lipodystrophy, congenital generalized, type 3", "Lipodystrophy, Congenital Generalized, Type 3", "LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 3", "type 3 Berardinelli-Seip congenital lipodystrophy", "Berardinelli-Seip congenital lipodystrophy type 3", "Berardinelli-Seip congenital lipodystrophy, type 3", "BERARDINELLI-SEIP CONGENITAL LIPODYSTROPHY, TYPE 3", "Berardinelli-Seip Congenital Lipodystrophy, Type 3", "LIPODYSTROPHY, BERARDINELLI-SEIP CONGENITAL, TYPE 3", "lipodystrophy, Berardinelli-Seip congenital, type 3", "Lipodystrophy, Berardinelli-Seip Congenital, Type 3", "CAV1 congenital generalized lipodystrophy (disease)", "congenital generalized lipodystrophy (disease) caused by mutation in CAV1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital generalized lipodystrophy type 3", "shortest_name_length": 4}
{"curie": "MONDO:0001541", "names": ["plantar nerve lesion", "lesion plantar nerve", "Plantar nerve lesion", "Lesion of plantar nerve", "lesion of plantar nerve", "Plantar nerve lesion NOS", "Lateral Plantar Neuropathy", "Lateral plantar neuropathy", "Plantar Neuropathy, Lateral", "Neuropathy, Lateral Plantar", "Lesion of plantar nerve, NOS", "Lateral Plantar Neuropathies", "Neuropathies, Lateral Plantar", "Lesion of lateral plantar nerve", "Plantar nerve lesion (disorder)", "plantar nerve lesion (diagnosis)", "plantar nerve peripheral nerve lesion", "Lateral plantar neuropathy (disorder)", "peripheral nerve lesion of plantar nerve", "Lesion of plantar nerve, unspecified lower limb"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "plantar nerve lesion", "shortest_name_length": 20}
{"curie": "MONDO:0011706", "names": ["KRS", "KRPPD", "PARK9", "park 9", "Parkinson disease 9", "Kufor-Rakeb syndrome", "Kufor Rakeb syndrome", "KUFOR-RAKEB SYNDROME", "Parkinson disease type 9", "PARK9 - Parkinson disease 9", "Kufor Rakeb syndrome (disorder)", "ceroid lipofuscinosis, neuronal, 12", "autosomal recessive Parkinson disease 9", "Parkinson disease 9, autosomal recessive", "autosomal recessive juvenile onset Parkinson disease 9", "PARKINSON DISEASE 9, AUTOSOMAL RECESSIVE, JUVENILE-ONSET", "Parkinson disease 9, autosomal recessive, juvenile-onset", "PALLIDOPYRAMIDAL DEGENERATION WITH SUPRANUCLEAR UPGAZE PARESIS AND DEMENTIA", "Pallidopyramidal Degeneration with Supranuclear Upgaze Paresis and Dementia", "Pallidopyramidal Degeneration with supranuclear upgaze paresis and dementia", "Pallidopyramidal degeneration with supranuclear upgaze paresis, and dementia", "KRPPD Kufor Rakeb pallidopyramidal degeneration with supranuclear upgaze paresis and dementia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kufor-Rakeb syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C1335981", "names": ["Small Cell Undifferentiated Hepatoblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Cell Undifferentiated Hepatoblastoma", "shortest_name_length": 42}
{"curie": "UMLS:C4682564", "names": ["Stage IVA Uterine Corpus Leiomyosarcoma", "Stage IVA Uterine Corpus Leiomyosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Uterine Corpus Leiomyosarcoma AJCC v8", "shortest_name_length": 39}
{"curie": "MONDO:0014657", "names": ["CILD32", "primary ciliary dyskinesia 32", "ciliary dyskinesia, primary, 32", "CILIARY DYSKINESIA, PRIMARY, 32", "RSPH3 primary ciliary dyskinesia", "primary ciliary dyskinesia type 32", "ciliary dyskinesia, primary, type 32", "primary ciliary dyskinesia 32 without situs inversus", "primary ciliary dyskinesia caused by mutation in RSPH3", "ciliary dyskinesia, primary, 32, without situs inversus", "CILIARY DYSKINESIA, PRIMARY, 32, WITHOUT SITUS INVERSUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia 32", "shortest_name_length": 6}
{"curie": "UMLS:C4744430", "names": ["Recurrent Desmoid Tumor", "Recurrent Desmoid Fibromatosis", "Recurrent Desmoid-Type Fibromatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Desmoid Fibromatosis", "shortest_name_length": 23}
{"curie": "MONDO:0010287", "names": ["SPG16", "spastic paraplegia 16", "X-linked spastic paraplegia 16", "spastic paraplegia 16, X-linked", "SPASTIC PARAPLEGIA 16, X-LINKED", "Spastic paraplegia 16, X-linked", "hereditary spastic paraplegia 16", "X-linked spastic paraplegia type 16", "hereditary spastic paraplegia type 16", "X-linked spastic paraplegia type 16 (disorder)", "spastic paraplegia 16, X-linked, complicated, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 16", "shortest_name_length": 5}
{"curie": "MONDO:0010759", "names": ["COA syndrome", "WILDERVANCK SYNDROME", "Wildervanck syndrome", "Wildervanck's syndrome", "Cervico-oculofacial syndrome", "Cervicooculoacoustic syndrome", "CERVICOOCULOACOUSTIC SYNDROME", "Wildervanck syndrome (disorder)", "Cervico-Oculo-Acoustic Syndrome", "cervico-oculo-acoustic syndrome", "cervico-oculo-acoustic dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wildervanck syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0012704", "names": ["CMD1X", "dilated cardiomyopathy 1X", "cardiomyopathy, dilated, 1X", "Cardiomyopathy, Dilated, 1x", "CARDIOMYOPATHY, DILATED, 1X", "dilated cardiomyopathy type 1X", "cardiomyopathy, dilated, type 1X", "FKTN familial isolated dilated cardiomyopathy", "dilated cardiomyopathy with mild or no proximal muscle weakness", "cardiomyopathy, dilated, with mild or No proximal muscle weakness", "CARDIOMYOPATHY, DILATED, WITH MILD OR NO PROXIMAL MUSCLE WEAKNESS", "Cardiomyopathy, Dilated, With Mild or No Proximal Muscle Weakness", "familial isolated dilated cardiomyopathy caused by mutation in FKTN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1X", "shortest_name_length": 5}
{"curie": "MONDO:0018213", "names": ["HSN1", "HSAN1", "HSAN 1", "HSAN I", "HSN Type I", "Type I, HSN", "HSAN Type I", "Type I, HSAN", "Acrodystrophic neuropathy", "hereditary sensory neuropathy type 1", "Hereditary Sensory Neuropathy Type I", "Hereditary Sensory Neuropathy Type 1", "Hereditary Sensory Neuropathy Type Ia", "Autosomal dominant sensory neuropathy", "Neuropathy, Hereditary Sensory, Type I", "Dominant hereditary sensory neuropathy, type I", "Hereditary Sensory Autonomic Neuropathy, Type 1", "Hereditary sensory neuropathy, type 1, dominant", "Autosomal dominant sensory neuropathy (disorder)", "neuropathy hereditary sensory and autonomic type 1", "Hereditary Sensory and Autonomic Neuropathy Type I", "Hereditary Sensory and Autonomic Neuropathy Type 1", "hereditary sensory and autonomic neuropathy type I", "Hereditary sensory and autonomic neuropathy type 1", "Neuropathy Hereditary Sensory and Autonomic Type 1", "hereditary sensory and autonomic neuropathy type 1", "Hereditary sensory and autonomic neuropathy type I", "Hereditary sensory and autonomic neuropathy, type I", "Neuropathy, Hereditary Sensory And Autonomic, Type I", "Neuropathy, Hereditary Sensory and Autonomic, Type I", "Neuropathy Hereditary Sensory Radicular, Autosomal Dominant", "neuropathy hereditary sensory radicular, autosomal dominant", "Neuropathy, Hereditary Sensory Radicular, Autosomal Dominant", "Hereditary sensory and autonomic neuropathy type I (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary sensory and autonomic neuropathy type 1", "shortest_name_length": 4}
{"curie": "MONDO:0100307", "names": ["adult Refsum disease due to PEX7 defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult Refsum disease due to PEX7 defect", "shortest_name_length": 39}
{"curie": "MONDO:0015441", "names": ["R7", "Ring 7", "r(7) syndrome", "rose cluster 7", "ROSE Cluster 7", "ring chromosome 7", "chromosome 7 ring", "Ring chromosome 7", "Ring chromosome type 7", "chromosome 7 ring syndrome", "Chromosome 7 ring syndrome", "Ring chromosome 7 syndrome", "ring chromosome 7 syndrome", "Ring chromosome 7 syndrome (disorder)", "Ring chromosome 7 syndrome (diagnosis)", "anomaly of chromosome pair ring chromosome 7 syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ring chromosome 7", "shortest_name_length": 2}
{"curie": "UMLS:C1257925", "names": ["Animal Mammary Carcinoma", "Carcinoma, Animal Mammary", "Animal Mammary Carcinomas", "Mammary Carcinoma, Animal", "Mammary Carcinomas, Animal", "Carcinomas, Animal Mammary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mammary Carcinoma, Animal", "shortest_name_length": 24}
{"curie": "MONDO:0015446", "names": ["Midaortic syndrome", "mid-aortic syndrome", "Mid aortic syndrome", "Mid-aortic syndrome", "middle aortic syndrome", "Middle aortic syndrome", "Atypical coarctation of aorta", "atypical coarctation of aorta", "Mid-aortic dysplastic syndrome", "mid-aortic dysplastic syndrome", "Middle aortic syndrome (disorder)", "Coarctation of the abdominal aorta", "coarctation of the abdominal aorta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical coarctation of aorta", "shortest_name_length": 18}
{"curie": "MONDO:0014342", "names": ["OOMD", "OOMD1", "oocyte maturation defect", "oocyte maturation defect 1", "OOCYTE MATURATION DEFECT 1", "female infertility due to zona pellucida defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "female infertility due to zona pellucida defect", "shortest_name_length": 4}
{"curie": "UMLS:C1333860", "names": ["Grade 2 Colorectal Adenocarcinoma", "Grade II Colorectal Adenocarcinoma", "Low Grade Colorectal Adenocarcinoma", "Moderately Differentiated Colorectal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade 2 Colorectal Adenocarcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0016284", "names": ["cervical peripheral neuroectodermal cancer", "peripheral neuroectodermal cancer of cervix uteri", "primitive neuroectodermal tumor of the cervix uteri", "cervical malignant peripheral neuroectodermal tumor", "malignant peripheral neuroectodermal tumor of the cervix uteri"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primitive neuroectodermal tumor of the cervix uteri", "shortest_name_length": 42}
{"curie": "MONDO:0012945", "names": ["ALS11", "ALS11 (diagnosis)", "Amyotrophic Lateral Sclerosis 11", "amyotrophic lateral sclerosis 11", "AMYOTROPHIC LATERAL SCLEROSIS 11", "FIG4 amyotrophic lateral sclerosis", "amyotrophic lateral sclerosis ALS11", "amyotrophic lateral sclerosis type 11", "amyotrophic lateral sclerosis caused by mutation in FIG4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyotrophic lateral sclerosis type 11", "shortest_name_length": 5}
{"curie": "UMLS:C1737211", "names": ["Hypoglycemic unconsciousness", "Hypoglycaemic unconsciousness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypoglycemic unconsciousness", "shortest_name_length": 28}
{"curie": "MONDO:0007340", "names": ["CCD", "CLCD", "CLCD1", "Marie-Sainton disease", "mutational dysostosis", "Marie-Sainton Disease", "osteodental dysplasia", "Marie Sainton Syndrome", "Marie-Sainton Syndrome", "craniocleidodysostosis", "Marie-Sainton syndrome", "Craniocleidodysostosis", "Cleidocranial Dysplasia", "cleidocranial dysplasia", "Syndrome, Marie-Sainton", "dysplasia cleidocranial", "Cleidocranial dysplasia", "dysostosis generalisata", "dysplasia cleidofacialis", "dysostosis cleidocranial", "Cleidocranial Dysostoses", "Dysplasia, Cleidocranial", "Cleidocranial Dysostosis", "Cleidocranial dysostosis", "CLEIDOCRANIAL DYSOSTOSIS", "Cleidocranial Dysplasias", "cleidocranial dysostosis", "cleidocranial dysplasia 1", "Dysostosis, Cleidocranial", "dysplasia cleidocranialis", "cleidocranial; dysostosis", "dysostosis; cleidocranial", "Dysostoses, Cleidocranial", "Dysplasias, Cleidocranial", "CLEIDOCRANIAL DYSPLASIA 1", "dysostosis cleidocranialis", "osteodental dysplasia (ODD)", "CCD - Cleidocranial dysplasia", "dysostosis cleidocraniopelvina", "CLCD - Cleidocranial dysplasia", "pelvicocleidocranial dysostosis", "dysostosis cleidocraniodigitalis", "Cleidocranial Digital Dysostoses", "Cleidocranial Digital Dysostosis", "cleidocranial digital dysostosis", "Dysostoses, Cleidocranial Digital", "Dysostosis, Cleidocranial Digital", "Cleidocranial dysostosis syndrome", "Scheuthauer-Marie-Sainton syndrome", "Scheuthauer-Marie-Sainton Syndrome", "Scheuthauer Marie Sainton Syndrome", "Cleidocranial dysostosis (disorder)", "cleidocranial dysplasia (CCD, CLCD)", "Syndrome, Scheuthauer-Marie-Sainton", "cleidocranial dysostosis (diagnosis)", "cleidocranial dysplasia, forme fruste, with brachydactyly", "CLEIDOCRANIAL DYSPLASIA 1, FORME FRUSTE, WITH BRACHYDACTYLY", "cleidocranial dysplasia, forme fruste, dental anomalies only", "CLEIDOCRANIAL DYSPLASIA 1, FORME FRUSTE, DENTAL ANOMALIES ONLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleidocranial dysplasia 1", "shortest_name_length": 3}
{"curie": "MONDO:0002002", "names": ["Postsurgical hypothyroidism", "postsurgical hypothyroidism", "post-surgical hypothyroidism", "Post surgical hypothyroidism", "Post-surgical hypothyroidism", "postsurgical; hypothyroidism", "postoperative hypothyroidism", "hypothyroidism; postsurgical", "Hypothyroidism postoperative", "Postoperative hypothyroidism", "Hypothyroidism after surgery", "Post-operative hypothyroidism", "postsurgical primary hypothyroidism", "Postoperative hypothyroidism (disorder)", "postsurgical primary hypothyroidism (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postsurgical hypothyroidism", "shortest_name_length": 27}
{"curie": "MONDO:0002722", "names": ["Olfactory Nerve Tumor", "olfactory nerve tumor", "olfactory neural tumor", "Olfactory Neural Tumor", "tumor of olfactory nerve", "Tumor of olfactory tract", "Olfactory Nerve Neoplasm", "olfactory nerve neoplasm", "Tumor of Olfactory Nerve", "olfactory nerve neoplasms", "Cranial Nerve I Neoplasms", "first cranial nerve tumor", "Tumour of olfactory tract", "cranial nerve I neoplasms", "First Cranial Nerve Tumor", "Olfactory Nerve Neoplasms", "Olfactory Neural Neoplasm", "olfactory neural neoplasm", "Neoplasms, Cranial Nerve I", "Neoplasms, Olfactory Nerve", "neoplasms, cranial nerve I", "neoplasms, olfactory nerve", "neoplasm of olfactory nerve", "Neoplasm of olfactory nerve", "Neoplasm of Olfactory Nerve", "Tumor of the Olfactory Nerve", "Tumor of First Cranial Nerve", "tumor of the olfactory nerve", "first cranial nerve neoplasm", "tumor of first cranial nerve", "First Cranial Nerve Neoplasm", "first cranial nerve neoplasms", "First Cranial Nerve Neoplasms", "Neoplasm of the Olfactory Nerve", "Neoplasm of First Cranial Nerve", "neoplasm of the olfactory nerve", "neoplasm of olfactory nerve (I)", "neoplasm of first cranial nerve", "Tumor of the First Cranial Nerve", "tumor of the first cranial nerve", "olfactory nerve neoplasm (disease)", "Neoplasm of the First Cranial Nerve", "neoplasm of the first cranial nerve", "Neoplasm of olfactory nerve (disorder)", "neoplasm of olfactory nerve (I) (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "olfactory nerve neoplasm", "shortest_name_length": 21}
{"curie": "MONDO:0010749", "names": ["SAMES", "Say Meyer syndrome", "SAY-MEYER SYNDROME", "Say-Meyer syndrome", "trigonocephaly, short stature and developmental delay", "Trigonocephaly, short stature and developmental delay", "trigonocephaly with short stature and developmental delay", "TRIGONOCEPHALY WITH SHORT STATURE AND DEVELOPMENTAL DELAY", "Trigonocephaly-short stature-developmental delay syndrome", "trigonocephaly-short stature-developmental delay syndrome", "Trigonocephaly with Short Stature and Developmental Delay", "Trigonocephaly, short stature, developmental delay syndrome", "trigonocephaly, short stature, developmental delay syndrome", "trigonocephaly, short stature, and retarded psychomotor development", "Trigonocephaly, short stature, and retarded psychomotor development", "Trigonocephaly, short stature, developmental delay syndrome (disorder)", "trigonocephaly, short stature, developmental delay syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trigonocephaly-short stature-developmental delay syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0012322", "names": ["HPE5", "holoprosencephaly 5", "Holoprosencephaly 5", "HOLOPROSENCEPHALY 5", "ZIC2 holoprosencephaly", "holoprosencephaly type 5", "Holoprosencephaly Type 5", "holoprosencephaly caused by mutation in ZIC2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "holoprosencephaly 5", "shortest_name_length": 4}
{"curie": "MONDO:0001404", "names": ["ecthyma", "ECTHYMA", "Ecthyma", "Ecthyma (disorder)", "ecthyma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ecthyma", "shortest_name_length": 7}
{"curie": "MONDO:0010865", "names": ["ASSA", "aminopterin-like syndrome", "PSEUDOAMINOPTERIN SYNDROME", "Pseudoaminopterin syndrome", "pseudoaminopterin syndrome", "aminopterin-like embryopathy", "fetal aminopterin-like syndrome", "aminopterin syndrome sine aminopterin", "Aminopterin syndrome sine aminopterin", "AMINOPTERIN SYNDROME SINE AMINOPTERIN", "Pseudoaminopterin syndrome (disorder)", "aminopterin syndrome-like sine aminopterin", "Aminopterin syndrome-like sine aminopterin", "aminopterin-like syndrome without aminopterin", "aminopterin syndrome sine aminopterin (ASSAS)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudoaminopterin syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0751850", "names": ["Heavy Metal Poisoning, Nervous System", "Poisoning, Heavy Metals, Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Heavy Metal Poisoning, Nervous System", "shortest_name_length": 37}
{"curie": "MONDO:0002078", "names": ["dysraphia", "dysraphism", "Dysraphism", "dysrhaphia", "defect septal", "Septal defect", "septal defect", "Septal defects", "failure fusion", "Dysraphia, NOS", "septum; defect", "defects septal", "defect; septum", "fusion failure", "Dysraphism, NOS", "Dysrhaphia, NOS", "Dysrhaphism, NOS", "Congenital cleft", "Septal defect NOS", "Imperfect closure", "Congenital fissure", "holes in the heart", "Holes in the Heart", "Heart Septal Defect", "heart septal defect", "defect heart septal", "septal defect heart", "Heart septal defect", "septal heart defect", "Heart septal defects", "heart septal defects", "Defect, Heart Septal", "Heart Septal Defects", "Septal Defect, Heart", "Defects, Heart Septal", "Septal Defects, Heart", "cardiac septal defect", "CARDIAC SEPTAL DEFECT", "Cardiac septal defect", "Cardiac Septal Defect", "Congenital cleft, NOS", "Septal Defect, Cardiac", "heart; anomaly, septum", "Cardiac Septal Defects", "anomaly; heart, septum", "Cardiac septal defects", "Defect, Cardiac Septal", "Congenital fissure, NOS", "Defects, Cardiac Septal", "Septal Defects, Cardiac", "deformity; heart, septum", "congenital septal defect", "heart; deformity, septum", "Congenital Septal Defect", "Congenital septal defect", "Congenital septal defects", "Septal (heart) defect NOS", "congenital defects septal", "Cardiac septal defect NOS", "Patent embryonic structure", "Congenital imperfect closure", "Congenital failure of fusion", "Congenital Failures of Fusion", "CONGENITAL FAILURES OF FUSION", "Failure of fusion, congenital", "Congenital septal defect, NOS", "CONGENITAL INCOMPLETE CLOSURES", "Congenital Incomplete Closures", "congenital heart septum defect", "Incomplete closure, congenital", "Patent embryonic structure, NOS", "Congenital heart defects, septal", "Abnormality of the cardiac septa", "CARDIAC SEPTAL DEFECT CONGENITAL", "Congenital cardiac septal defect", "congenital septal defect of heart", "Congenital failure of fusion, NOS", "Cardiac septal defects (disorder)", "Congenital defective closure, NOS", "Cardiac septal defects congenital", "Congenital septal defect of heart", "Congenital incomplete closure, NOS", "Abnormal cardiac septum morphology", "Congenital cardiac septal defect NOS", "congenital septal defect (diagnosis)", "Congenital cardiac septal defect, NOS", "Congenital septal defect of heart, NOS", "Congenital malformations of cardiac septa", "Congenital septal defect of heart (disorder)", "Congenital septal defect (morphologic abnormality)", "Congenital malformation of cardiac septum, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heart septal defect", "shortest_name_length": 9}
{"curie": "MONDO:0014777", "names": ["IHPRF2", "HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2", "hypotonia, infantile, with psychomotor retardation and characteristic facies 2", "UNC80 hypotonia, infantile, with psychomotor retardation and characteristic facies", "hypotonia, infantile, with psychomotor retardation and characteristic facies type 2", "hypotonia, infantile, with psychomotor retardation and characteristic facies 2; IHPRF2", "hypotonia, infantile, with psychomotor retardation and characteristic facies caused by mutation in UNC80"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotonia, infantile, with psychomotor retardation and characteristic facies 2", "shortest_name_length": 6}
{"curie": "UMLS:C3273218", "names": ["Invasive Breast Lobular Carcinoma, Tubulolobular Variant", "Invasive Lobular Breast Carcinoma, Tubulolobular Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Invasive Breast Lobular Carcinoma, Tubulolobular Variant", "shortest_name_length": 56}
{"curie": "MONDO:0100087", "names": ["FAD", "GARD:0000632", "familial Alzheimer disease", "Alzheimer disease, familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial Alzheimer disease", "shortest_name_length": 3}
{"curie": "MONDO:0006738", "names": ["Poroma", "poroma", "Acrospiroma", "hidradenoma", "Hidradenoma", "Spiradenoma", "acrospiromas", "Hidradenomas", "Spiradenomas", "Acrospiromas", "eccrine poroma", "Eccrine Poroma", "Eccrine poroma", "Poroma, Eccrine", "Eccrine Poromas", "[M]Eccrine poroma", "poroma/acrospiroma", "nodular hidradenoma", "Eccrine Spiradenoma", "Nodular Hidradenoma", "Eccrine Acrospiroma", "eccrine acrospiroma", "Nodular hidradenoma", "eccrine hidradenoma", "Eccrine acrospiroma", "Eccrine hidradenoma", "acrospiroma, eccrine", "Spiradenoma, Eccrine", "Eccrine Spiradenomas", "eccrine Acrospiromas", "poroma (acrospiroma)", "Eccrine Acrospiromas", "nodular Hidradrenoma", "Acrospiroma, Eccrine", "nodular Hidradrenomas", "Hidradrenoma, nodular", "Spiradenomas, Eccrine", "acrospiromas, eccrine", "Eccrine poroma of skin", "[M]Eccrine acrospiroma", "Hidradrenomas, nodular", "clear cell hidradenoma", "clear-cell Hidradrenoma", "clear cell Hidradrenoma", "Solid-cystic hidradenoma", "Hidradrenoma, clear-cell", "clear-cell Hidradrenomas", "solid cystic hidradenoma", "solid-cystic hidradenoma", "solid-cystic Hidradenomas", "hidradenoma, solid-cystic", "Hidradrenomas, clear-cell", "Hidradenomas, solid-cystic", "Eccrine nodular hidradenoma", "Eccrine hidradenoma of skin", "eccrine hidradenoma of skin", "Solid and Cystic Hidradenoma", "Apocrine nodular hidradenoma", "Eccrine poroma of skin (disorder)", "Eccrine hidradenoma of skin (disorder)", "Eccrine poroma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eccrine acrospiroma", "shortest_name_length": 6}
{"curie": "MONDO:0002352", "names": ["ca larynx", "Larynx cancer", "cancer larynx", "larynx cancer", "Larynx Cancer", "Cancer, Larynx", "Larynx--Cancer", "Larynx Cancers", "Cancers, Larynx", "cancer of larynx", "Laryngeal cancer", "LARYNGEAL CANCER", "Cancer of Larynx", "Cancer of larynx", "cancer laryngeal", "laryngeal cancer", "of larynx cancer", "Laryngeal Cancer", "Cancer, Laryngeal", "Laryngeal Cancers", "Cancers, Laryngeal", "Laryngeal cancer NOS", "cancer of the larynx", "Cancer of the Larynx", "Neoplasm malig;larynx", "CA - Cancer of larynx", "Malignant Larynx Tumor", "malignant larynx tumor", "malignant tumor of larynx", "Malignant Laryngeal Tumor", "Larynx neoplasm malignant", "LARYNX NEOPLASM MALIGNANT", "malignant laryngeal tumor", "Malignant tumor of larynx", "Malignant Larynx Neoplasm", "malignant larynx neoplasm", "Malignant Tumor of Larynx", "LARYNGEAL CANCER MALIGNANT", "Malignant tumour of larynx", "Malignant Laryngeal Neoplasm", "laryngeal cancer (diagnosis)", "malignant neoplasm of larynx", "Malignant neoplasm of larynx", "malignant laryngeal neoplasm", "Malignant Neoplasm of Larynx", "Laryngeal neoplasms malignant", "malignant tumor of the larynx", "Malignant Tumor of the Larynx", "malignant neoplasm of the larynx", "Malignant Neoplasm of the Larynx", "malignant neosplasm of the larynx", "Malignant neoplasm of larynx, NOS", "Malignant tumor of larynx (disorder)", "malignant neoplasm of larynx (diagnosis)", "Malignant neoplasm of larynx, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "larynx cancer", "shortest_name_length": 9}
{"curie": "MONDO:0003929", "names": ["Micropapillomatosis Labialis", "micropapillomatosis labialis", "vestibular micropapillomatosis", "Vestibular Micropapillomatosis", "Vulvar Squamous Cell Papillomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vestibular micropapillomatosis", "shortest_name_length": 28}
{"curie": "UMLS:C4524683", "names": ["Melanoma Metastatic in the CNS", "Melanoma Metastatic in the Central Nervous System", "Metastatic Melanoma in the Central Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Melanoma Metastatic in the Central Nervous System", "shortest_name_length": 30}
{"curie": "MONDO:0018971", "names": ["Oxycephaly", "oxycephaly", "High skull", "acrocephaly", "Acrocephaly", "tower skull", "Tower skull", "ACROCEPHALY", "hypsocephaly", "hypsicephaly", "turricephaly", "Turricephaly", "pyrgocephaly", "Turricephalus", "skull elongated", "elongated skull", "Elongated skull", "Egg-shaped skull", "Tall shaped head", "Tower skull shape", "Tall shaped skull", "acrocephalic skull", "isolated oxycephaly", "Tower cranium shape", "Tall shaped cranium", "Acrocephaly (disorder)", "acrocephaly was observed", "skull elongated (physical finding)", "acrocephalic skull (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated oxycephaly", "shortest_name_length": 10}
{"curie": "MONDO:0013238", "names": ["Del(17)(q23.1q23.2)", "monosomy 17q23.1q23.2", "Monosomy 17q23.1q23.2", "monosomy 17q23.1-q23.2", "17q23.1q23.2 microdeletion syndrome", "17q23.1-q23.2 microdeletion syndrome", "chromosome 17q23.1-q23.2 deletion syndrome", "CHROMOSOME 17q23.1-q23.2 DELETION SYNDROME", "17q23.1q23.2 microdeletion syndrome (disorder)", "chromosome 17q23.1-q23.2 deletion syndrome, isolated cases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 17q23.1-q23.2 deletion syndrome", "shortest_name_length": 19}
{"curie": "UMLS:C4521808", "names": ["Stage I Appendix Cancer", "Stage I Appendix Carcinoma AJCC v8", "Stage I Appendiceal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Appendix Carcinoma AJCC v8", "shortest_name_length": 23}
{"curie": "MONDO:0002337", "names": ["intra-abdominal hemangioma", "Intra-Abdominal Hemangioma", "Intra-abdominal hemangioma", "Intra-abdominal haemangioma", "hemangioma, intra-abdominal", "hemangioma, Intra-abdominal", "Hemangioma, Intra-Abdominal", "abdominal cavity hemangioma", "hemangioma of abdominal cavity", "hemangioma intra-abdominal structures", "Hemangioma of Intra-Abdominal Structure", "Hemangioma of intra-abdominal structure", "hemangioma of intra-abdominal structure", "Haemangioma of intra-abdominal structure", "Hemangioma of intra-abdominal structures", "hemangioma of intra-abdominal structures", "Haemangioma of intra-abdominal structures", "hemangioma intra-abdominal structures (diagnosis)", "Hemangioma of intra-abdominal structure (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intra-abdominal hemangioma", "shortest_name_length": 26}
{"curie": "UMLS:C0033775", "names": ["anal itch", "itch anal", "Anal itch", "anal; itch", "itch; anal", "rectal itch", "Anal itching", "ani pruritis", "Pruritus Ani", "PRURITUS ANI", "Itching;anal", "pruritus ani", "ani pruritus", "itching anal", "PRURITIS ANI", "pruritis ani", "anal itching", "Pruritus ani", "Perianal itch", "ANAL PRURITUS", "pruritus; ani", "pruritus anal", "Anal pruritus", "anis pruritus", "anal pruritus", "ani; pruritus", "Itching;rectal", "itching rectal", "rectal itching", "rectal pruritus", "itching perianal", "Itching;perianal", "Perianal itching", "perianal itching", "PERIANAL ITCHING", "Pruritus;perianal", "perianal pruritus", "Pruritus perineal", "Perianal irritation", "irritations perianal", "anal itching (symptom)", "itching in anal region", "Pruritus ani (disorder)", "pruritus ani (diagnosis)", "rectal itching (symptom)", "pruritis of perianal region", "pruritus in the anal region", "itching in anal region (symptom)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pruritus Ani", "shortest_name_length": 9}
{"curie": "MONDO:0019624", "names": ["AAE", "acquired angioedema", "Acquired angioedema", "angioedema, acquired", "Acquired angio-oedema", "acquired angioneurotic edema", "Acquired angioneurotic edema", "Acquired C1 inhibitor deficiency", "acquired C1 inhibitor deficiency", "acquired bradykinine-induced angioedema", "Acquired bradykinine-induced angioedema", "Acquired non histamine-induced angioedema", "acquired non histamine-induced angioedema", "Acquired C1 esterase inhibitor deficiency", "Acquired angioedema with C1Inh deficiency", "acquired C1 inhibitor deficiency (diagnosis)", "Acquired angioneurotic edema with C1Inh deficiency", "Acquired C1 esterase inhibitor deficiency (disorder)", "Acquired angioneurotic edema with C1 inhibitor deficiency", "Acquired angioneurotic oedema with C1 inhibitor deficiency", "Acquired angioedema with C1Inh (C1 esterase inhibitor) deficiency", "Acquired angioneurotic edema with C1Inh (C1 esterase inhibitor) deficiency", "Acquired angioneurotic oedema with C1Inh (C1 esterase inhibitor) deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired angioedema", "shortest_name_length": 3}
{"curie": "MONDO:0019975", "names": ["pellagra", "Pellagra", "PELLAGRA", "Pellagras", "deficiency niacin", "pellagra disorder", "niacin deficiency", "Niacin deficiency", "niacin; deficiency", "deficiency; niacin", "Pellagra (disorder)", "deficiencies niacin", "pellagra (diagnosis)", "Vitamin B3 deficiency", "Vitamin PP deficiency", "vitamin b3 deficiency", "nicotinamide deficiency", "Nicotinamide deficiency", "nicotinamide; deficiency", "deficiency; nicotinamide", "nicotinic acid deficiency", "VITAMIN DEFICIENCY NIACIN", "Nicotinic acid deficiency", "Niacin deficiency disease", "NIACIN DEFICIENCY PELLAGRA", "nicotinic acid; deficiency", "deficiency; nicotinic acid", "niacin-tryptophan deficiency", "Niacin deficiency [pellagra]", "NIACIN DEFICIENCY <PELLAGRA>", "Niacin deficiency (disorder)", "Niacin-tryptophan deficiency", "Niacin (-tryptophan) deficiency", "Vitamin B3 deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pellagra", "shortest_name_length": 8}
{"curie": "UMLS:C4684867", "names": ["Refractory Hepatoblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Hepatoblastoma", "shortest_name_length": 25}
{"curie": "UMLS:C1333457", "names": ["Low Grade Esophageal Glandular Dysplasia", "Low Grade Esophageal Glandular Intraepithelial Neoplasia", "Esophageal Low Grade Glandular Intraepithelial Neoplasia", "Esophageal glandular dysplasia (intraepithelial neoplasia), low grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Grade Esophageal Glandular Intraepithelial Neoplasia", "shortest_name_length": 40}
{"curie": "MONDO:0005500", "names": ["MPI-CDG", "DPM2-CDG", "ALG9-CDG", "ALG8-CDG", "ALG3-CDG", "DOLK-CDG", "DPM1-CDG", "PMM2-CDG", "ALG2-CDG", "RFT1-CDG", "ALG6-CDG", "ALG1-CDG", "DPM3-CDG", "ALG11-CDG", "ALG12-CDG", "MPDU1-CDG", "DPAGT1-CDG", "SRD5A3-CDG", "MPI-CDG (CDG-1b)", "ALG8-CDG (CDG-1h)", "DPM2-CDG (CDG-1u)", "RFT1-CDG (CDG-1n)", "ALG9-CDG (CDG-1l)", "DPM1-CDG (CDG-1e)", "DPM3-CDG (CDG-1o)", "ALG6-CDG (CDG-1c)", "ALG1-CDG (CDG-1k)", "ALG2-CDG (CDG-1i)", "ALG3-CDG (CDG-1d)", "DOLK-CDG (CDG-1m)", "PMM2-CDG (CDG-1a)", "ALG11-CDG (CDG-1p)", "MPDU1-CDG (CDG-1f)", "ALG12-CDG (CDG-1g)", "SRD5A3-CDG (CDG-1q)", "DPAGT1-CDG (CDG-1j)", "congenital disorder of glycosylation type I", "congenital disorders of glycosylation, type I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital disorder of glycosylation type I", "shortest_name_length": 7}
{"curie": "MONDO:0006094", "names": ["Askin tumor", "ASKIN TUMOR", "askin tumor", "Askin Tumor", "Askin tumour", "Askin's Tumor", "Askin's tumor", "askin's tumor", "askin's tumors", "Askin's tumour", "PNET of chest wall", "PNET of Thoracopulmonary Region", "PNET of thoracopulmonary region", "Askin tumor (morphologic abnormality)", "small cell tumor of thoracopulmonary region", "Small Cell Tumor of Thoracopulmonary Region", "peripheral neuroectodermal tumor of thoracopulmonary region", "Peripheral Neuroectodermal Tumor of Thoracopulmonary Region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Askin tumor", "shortest_name_length": 11}
{"curie": "MONDO:0002536", "names": ["WART", "Wart", "papilloma skin", "Papilloma skin", "PAPILLOMA SKIN", "Skin papilloma", "skin papilloma", "Skin Papilloma", "papillomas skin", "Papillomata;skin", "skin papillomata", "papilloma of skin", "Papilloma of Skin", "Papilloma of skin", "papilloma cutaneous", "Cutaneous Papilloma", "cutaneous papilloma", "papilloma of the skin", "Papilloma of the Skin", "zone of skin papilloma", "basosquamous tumor, benign", "BASOSQUAMOUS TUMOR, BENIGN", "Papilloma of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin papilloma", "shortest_name_length": 4}
{"curie": "UMLS:C4521712", "names": ["IV", "Stage IV Esophageal Adenocarcinoma", "Pathologic Stage IV Esophageal Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IV Esophageal Adenocarcinoma AJCC v8", "shortest_name_length": 2}
{"curie": "MONDO:0001923", "names": ["Vitreoretinal dystrophy", "vitreoretinal dystrophy", "dystrophy; vitreoretinal", "vitreoretinal; dystrophy", "Vitreoretinal dystrophies", "vitreoretinal dystrophies", "Vitreoretinal dystrophy (disorder)", "vitreoretinal dystrophy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitreoretinal dystrophy", "shortest_name_length": 23}
{"curie": "MONDO:0004631", "names": ["Tongue Cancer", "cancer tongue", "tongue cancer", "TONGUE CANCER", "Tongue Cancers", "Cancer, Tongue", "Tongue--Cancer", "tongue cancers", "Cancers, Tongue", "of tongue cancer", "cancer of tongue", "Cancer of tongue", "Cancer of Tongue", "tongue carcinoma", "Tongue Neoplasms", "Cancer of the Tongue", "cancer of the tongue", "CA - Cancer of tongue", "Neoplasm malig;tongue", "Malignant Tongue Tumor", "malignant tongue tumor", "TONGUE CANCER MALIGNANT", "malignant tongue cancer", "Malignant tongue cancer", "Malignant Tongue Neoplasm", "tongue neoplasm malignant", "malignant tongue neoplasm", "Malignant tumor of tongue", "Malignant tongue neoplasm", "Malignant Tumor of Tongue", "malignant tumor of tongue", "Tongue Neoplasm, Malignant", "Malignant tumour of tongue", "tongue neoplasm, malignant", "malignant neoplasm of tongue", "Malignant neoplasm of tongue", "TONGUE BASE CANCER MALIGNANT", "Malignant Neoplasm of Tongue", "Malignant Tumor of the Tongue", "malignant tumor of the tongue", "Malignant Base of Tongue Tumor", "malignant neoplasm of the tongue", "Malignant Posterior Tongue Tumor", "Malignant Neoplasm of the Tongue", "Malignant neoplasm of tongue NOS", "tongue neoplasm malignant border", "malignant neoplasm of tongue NOS", "malignant neoplasm of tongue, NOS", "malignant tumor of lingual tonsil", "Malignant neoplasm of tongue, NOS", "Malignant tumor of base of tongue", "Malignant Base of Tongue Neoplasm", "malignant tumor of base of tongue", "Malignant tumor of lingual tonsil", "Malignant Tumor of Base of Tongue", "Malignant tumour of base of tongue", "Malignant Base of the Tongue Tumor", "Malignant tumour of lingual tonsil", "malignant neoplasm of dorsal tongue", "Malignant Tumor of Posterior Tongue", "malignant tumor of posterior tongue", "Malignant Posterior Tongue Neoplasm", "malignant neoplasm of base of tongue", "Malignant Neoplasm of Base of Tongue", "Malignant tumor of tongue (disorder)", "malignant neoplasm of lingual tonsil", "Malignant neoplasm of base of tongue", "Malignant neoplasm of lingual tonsil", "Malignant Base of the Tongue Neoplasm", "malignant neoplasm of dorsum of tongue", "malignant neoplasm of border of tongue", "Malignant neoplasm of border of tongue", "Malignant Neoplasm of Posterior Tongue", "Malignant tumor of fixed part of tongue", "malignant neoplasm of dorsal tongue NOS", "Malignant Tumor of the Posterior Tongue", "Malignant neoplasm of dorsal tongue NOS", "malignant neoplasm of tongue (diagnosis)", "Malignant tumour of fixed part of tongue", "Malignant tumor of mobile part of tongue", "malignant tumor of mobile part of tongue", "Malignant neoplasm of tongue, unspecified", "Malignant Tumor of the Base of the Tongue", "Malignant tumour of mobile part of tongue", "malignant neoplasm of fixed part of tongue", "Malignant Neoplasm of the Posterior Tongue", "malignant tumor of dorsal surface of tongue", "Tongue Neoplasm Malignant Stage Unspecified", "malignant neoplasm of other sites of tongue", "tongue neoplasm malignant stage unspecified", "malignant neoplasm of mobile part of tongue", "Tongue neoplasm malignant stage unspecified", "malignant tumor of lingual tonsil (disorder)", "Malignant tumor of posterior third of tongue", "malignant neoplasm of ventral tongue surface", "malignant tumor of junctional zone of tongue", "Malignant tumor of lingual tonsil (disorder)", "Malignant tumor of junctional zone of tongue", "malignant neoplasm of anterior 2/3 of tongue", "Malignant tumor of base of tongue (disorder)", "malignant tumor of ventral surface of tongue", "Malignant Neoplasm of the Base of the Tongue", "Malignant neoplasm of tongue, junctional zone", "Malignant tumour of posterior third of tongue", "Malignant tumour of junctional zone of tongue", "malignant neoplasm of dorsal surface of tongue", "malignant neoplasm of fixed part of tongue NOS", "Malignant neoplasm of dorsal surface of tongue", "Malignant neoplasm of fixed part of tongue NOS", "Malignant neoplasm of junctional zone of tongue", "Malignant neoplasm of mobile part of tongue NOS", "malignant neoplasm of ventral surface of tongue", "malignant neoplasm of junctional zone of tongue", "Malignant neoplasm of ventral surface of tongue", "Malignant neoplasm of posterior third of tongue", "malignant neoplasm of mobile part of tongue NOS", "malignant neoplasm of base of tongue (diagnosis)", "Malignant tumor of anterior two-thirds of tongue", "malignant tumor of anterior two-thirds of tongue", "malignant neoplasm of lingual tonsil (diagnosis)", "Malignant neoplasm of border of tongue (disorder)", "Malignant tumour of anterior two-thirds of tongue", "malignant neoplasm of border of tongue (diagnosis)", "malignant tumor of tip and lateral border of tongue", "malignant neoplasm of anterior two-thirds of tongue", "Malignant neoplasm of tongue, tip and lateral border", "malignant neoplasm of tongue, tip and lateral border", "malignant neoplasm of tip and lateral border of tongue", "Malignant neoplasm of tip and lateral border of tongue", "Malignant tumor of tongue posterior to vallate papillae", "Malignant tumor of junctional zone of tongue (disorder)", "Malignant neoplasm of anterior two-thirds of tongue, NOS", "Malignant tumour of tongue posterior to vallate papillae", "Malignant neoplasm of dorsal surface of tongue (disorder)", "malignant neoplasm of tip and/or lateral border of tongue", "malignant neoplasm of dorsal surface of tongue (diagnosis)", "malignant neoplasm of junctional zone of tongue (diagnosis)", "malignant neoplasm of ventral surface of tongue (diagnosis)", "Malignant tumor of anterior two-thirds of tongue (disorder)", "Malignant neoplasm of tongue, tip and lateral border (disorder)", "malignant neoplasm of anterior two-thirds of tongue (diagnosis)", "malignant neoplasm of tip and lateral border of tongue (diagnosis)", "Malignant neoplasm of anterior two-thirds of tongue, part unspecified", "malignant neoplasm of anterior two-thirds of tongue, part unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tongue cancer", "shortest_name_length": 13}
{"curie": "MONDO:0042489", "names": ["diatheses", "diathesis", "Disease Susceptibility", "disease susceptibility", "susceptibility, disease", "disease susceptibilities", "susceptibilities, disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disease susceptibility", "shortest_name_length": 9}
{"curie": "UMLS:C1328315", "names": ["Hypercreatininemia", "Hypercreatininaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypercreatininaemia", "shortest_name_length": 18}
{"curie": "MONDO:0020430", "names": ["Divided left atrium", "divided left atrium", "cor triatriatum sinister", "Cor triatriatum sinister", "cor triatriatum sinistrum", "Cor triatriatum sinistrum", "Divided left atrium (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cor triatriatum sinister", "shortest_name_length": 19}
{"curie": "MONDO:0013363", "names": ["dup(2)(q31.1)", "trisomy 2q31.1", "2q31.1 microduplication syndrome", "chromosome 2q31.1 duplication syndrome", "CHROMOSOME 2q31.1 DUPLICATION SYNDROME", "MESOMELIC DYSPLASIA, 2q31.1 DUPLICATION-RELATED", "mesomelic dysplasia, 2Q31.1 Duplication-related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 2q31.1 duplication syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0001208", "names": ["arf", "RESPIRATORY FAILURE ACUTE", "Acute respiratory failure", "acute respiratory failure", "acute failure respiratory", "Acute Respiratory Failure", "Respiratory failure, acute", "respiratory failure, acute", "ARF - Acute respiratory failure", "Acute respiratory failure (disorder)", "acute respiratory failure (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute respiratory failure", "shortest_name_length": 3}
{"curie": "MONDO:0016574", "names": ["Westerhof-Beemer-Cormane syndrome", "Westerhof Beemer Cormane syndrome", "congenital hypomelanotic and hypermelanotic macules", "Congenital hypomelanotic and hypermelanotic macules", "hereditary congenital hypopigmented and hyperpigmented macules", "Macules hereditary congenital hypopigmented and hyperpigmented", "Hereditary congenital hypopigmented and hyperpigmented macules", "macules hereditary congenital hypopigmented and hyperpigmented", "Macules, Hereditary Congenital Hypopigmented and Hyperpigmented", "macules, hereditary congenital hypopigmented and hyperpigmented", "Hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome", "hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome", "Hypo-and hypermelanotic cutaneous macules, retarded growth, intellectual disability syndrome", "Hereditary congenital hypomelanotic and hypermelanotic cutaneous macules, growth retardation, intellectual disability syndrome", "Hereditary congenital hypomelanotic and hypermelanotic cutaneous macules, growth retardation, intellectual disability syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome", "shortest_name_length": 33}
{"curie": "MONDO:0010175", "names": ["Hozay's syndrome", "Hozay’s syndrome", "VAN BOGAERT-HOZAY SYNDROME", "Van Bogaert-Hozay syndrome", "van Bogaert-Hozay syndrome", "acro-osteolysis-facial dysplasia syndrome", "Acro-osteolysis-facial dysplasia syndrome", "A familial form of acro-osteolysis associated with a mild mental retardation, skin atrophy, facial dysmorphism, and ocular defects", "A familial form of acro-osteolysis associated with a mild intellectual disability, skin atrophy, facial dysmorphism, and ocular defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "van Bogaert-Hozay syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0001039", "names": ["tonsilitis", "tonsillitis", "TONSILLITIS", "Tonsillitis", "Tonsillitides", "Tonsillitis NOS", "Tonsillitis, NOS", "chronic tonsillitis", "Chronic tonsillitis", "tonsillitis chronic", "TONSILLITIS CHRONIC", "tonsil inflammation", "Tonsillitis;chronic", "Tonsil Inflammation", "tonsils inflammation", "tonsillitis; chronic", "tonsil; inflammation", "chronic; tonsillitis", "Inflammation;tonsils", "TONSILLITIS, CHRONIC", "inflammation; tonsil", "inflammation tonsils", "Recurrent tonsillitis", "Tonsillitis recurrent", "recurrent tonsillitis", "TONSILLITIS RECURRENT", "Tonsillitis;recurrent", "inflammation of tonsil", "Tonsillitis (disorder)", "Inflammation of tonsil", "Tonsillar inflammation", "tonsillitis (diagnosis)", "Tonsillitis chronic NOS", "infection; tonsil, chronic", "tonsil; infection, chronic", "inflammation of the tonsils", "Throat infection - tonsillitis", "Chronic tonsillitis (disorder)", "throat infection - tonsillitis", "chronic tonsillitis (diagnosis)", "Recurrent inflammation of tonsils"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tonsillitis", "shortest_name_length": 10}
{"curie": "UMLS:C0919599", "names": ["Application site eczema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Application site eczema", "shortest_name_length": 23}
{"curie": "MONDO:0003369", "names": ["Vagina Leiomyosarcoma", "vagina leiomyosarcoma", "Vaginal Leiomyosarcoma", "vaginal leiomyosarcoma", "leiomyosarcoma of vagina", "Leiomyosarcoma of Vagina", "leiomyosarcoma of the vagina", "Leiomyosarcoma of the Vagina", "leiomyosarcoma of vagina (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vagina leiomyosarcoma", "shortest_name_length": 21}
{"curie": "MONDO:0003472", "names": ["lice", "Lice", "pediculosis", "PEDICULOSIS", "Pediculoses", "Pediculosis", "lice infestation", "Lice infestation", "Lice Infestation", "Infestation, Lice", "Lice Infestations", "mixed pediculosis", "Mixed pediculosis", "louse infestation", "Louse infestation", "mixed; pediculosis", "Infestations, Lice", "Pediculosis + lice", "pediculosis + lice", "pediculosis; mixed", "Lice infestation, NOS", "Pediculus; infestation", "infestation; Pediculus", "pediculosis (diagnosis)", "pediculosis; phthiriasis", "infestation by Pediculus", "Pediculosis, unspecified", "pediculosis, unspecified", "Infestation by Pediculus", "Pediculus humanus infection", "Pediculosis and phthiriasis", "Louse infestation (disorder)", "infections, Pediculus humanus", "mixed pediculosis infestation", "phthiriasis; with pediculosis", "Infestation by Pediculus, NOS", "Mixed pediculosis infestation", "Infestation caused by Pediculus", "pediculosis and Phthirus infection", "pediculosis and phthirus infection", "pediculosis and Phthirus infections", "Pediculosis and phthirus infections", "pediculosis and Phthirus infestation", "Pediculosis and phthirus infestation", "mixed pediculosis infestation (diagnosis)", "Infestation caused by Pediculus (disorder)", "Pediculosis and phthirus infections (disorder)", "louse infestation (& [pediculosis and Phthirus] or [lice])"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lice infestation", "shortest_name_length": 4}
{"curie": "UMLS:C2981679", "names": ["stage IIIB penile cancer", "Stage IIIB Penile Cancer", "Stage IIIb Penile Cancer", "stage IIIB penile cancer AJCC v7", "Stage IIIb Penile Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIb Penile Cancer AJCC v7", "shortest_name_length": 24}
{"curie": "MONDO:0018093", "names": ["Arbovirosis", "arbovirus fever"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arbovirus fever", "shortest_name_length": 11}
{"curie": "UMLS:C2984114", "names": ["Pharyngeal Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pharyngeal Carcinoma by AJCC v7 Stage", "shortest_name_length": 37}
{"curie": "MONDO:0019357", "names": ["congenital cervical spinal stenosis", "congenital stenosis of the cervical spine", "congenital narrowing of cervical spinal canal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital narrowing of cervical spinal canal", "shortest_name_length": 35}
{"curie": "MONDO:0013302", "names": ["NPHP11", "nephronophthisis 11", "NEPHRONOPHTHISIS 11", "nephronophthisis type 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephronophthisis 11", "shortest_name_length": 6}
{"curie": "UMLS:C5206594", "names": ["Paratesticular Paraganglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paratesticular Paraganglioma", "shortest_name_length": 28}
{"curie": "UMLS:C4682556", "names": ["Stage IA Uterine Corpus Leiomyosarcoma", "Stage IA Uterine Corpus Leiomyosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Uterine Corpus Leiomyosarcoma AJCC v8", "shortest_name_length": 38}
{"curie": "MONDO:0007116", "names": ["hemangiomatosis, disseminated", "HEMANGIOMATOSIS, DISSEMINATED", "Hemangiomatosis, Disseminated", "Hereditary neurocutaneous Angioma", "Angioma hereditary neurocutaneous", "angioma hereditary neurocutaneous", "hereditary neurocutaneous angioma", "angioma, hereditary neurocutaneous", "ANGIOMA, HEREDITARY NEUROCUTANEOUS", "Angioma, Hereditary Neurocutaneous", "Hereditary neurocutaneous angiomata", "hereditary neurocutaneous malformation", "Hereditary neurocutaneous angiomata (disorder)", "Hereditary neurocutaneous vascular malformations", "Spinal Arterial Venous Malformations with Cutaneous Hemangiomas", "SPINAL ARTERIAL VENOUS MALFORMATIONS WITH CUTANEOUS HEMANGIOMAS", "spinal arterial Venous malformations with cutaneous hemangiomas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary neurocutaneous angioma", "shortest_name_length": 29}
{"curie": "UMLS:C4528573", "names": ["Stage IB Breast Cancer", "Prognostic Stage IB Breast Cancer AJCC v8", "Prognostic Stage IB Breast Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prognostic Stage IB Breast Cancer AJCC v8", "shortest_name_length": 22}
{"curie": "MONDO:0014674", "names": ["MODY14", "maturity-onset diabetes of the young type 14", "MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 14", "maturity-onset diabetes of the young, type 14", "APPL1 maturity-onset diabetes of the young (disease)", "maturity-onset diabetes of the young (disease) caused by mutation in APPL1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maturity-onset diabetes of the young type 14", "shortest_name_length": 6}
{"curie": "MONDO:0003133", "names": ["exudative glomerulonephritis", "Exudative glomerulonephritis", "Exudative Glomerulonephritis", "Exudative glomerulonephritis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exudative glomerulonephritis", "shortest_name_length": 28}
{"curie": "UMLS:C5420342", "names": ["Salivary Gland MALT Lymphoma", "Salivary Gland Mucosa-Associated Lymphoid Tissue Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Salivary Gland Mucosa-Associated Lymphoid Tissue Lymphoma", "shortest_name_length": 28}
{"curie": "UMLS:C3698411", "names": ["Asymptomatic left ventricular systolic dysfunction", "Asymptomatic left ventricular systolic dysfunction (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Asymptomatic left ventricular systolic dysfunction", "shortest_name_length": 50}
{"curie": "MONDO:0004891", "names": ["Hyperopia", "HYPEROPIA", "hyperopia", "long sight", "Farsighted", "farsighted", "Long;sight", "Longsighted", "long sighted", "Long-sighted", "Hypermetropia", "hypermetropia", "farsightedness", "Farsightedness", "far sightedness", "far-sightedness", "Far-sightedness", "Longsightedness", "Long-sightedness", "Hypermetropia (disorder)", "hypermetropia (diagnosis)", "Hypermetropia (farsightedness)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperopia", "shortest_name_length": 9}
{"curie": "MONDO:0007308", "names": ["CMT2A", "CMT2A1", "CMT 2A", "HMSN2A1", "HMSN IIA", "HMSN IIa1", "HMSN IIA1", "Charcot Marie Tooth disease type 2A", "Charcot-Marie-Tooth disease Type 2A", "Charcot-Marie-Tooth disease type 2A", "Charcot-Marie-Tooth Disease Type 2A", "Charcot-Marie-Tooth disease type 2A1", "Charcot-Marie-Tooth disease, Type 2A", "Charcot-Marie-Tooth Disease Type 2A1", "Charcot-Marie-Tooth disease, type 2A1", "Charcot-Marie-Tooth neuropathy type 2A1", "Charcot-Marie-Tooth Neuropathy, Type 2A1", "KIF1B Charcot-Marie-Tooth disease type 2", "Charcot-Marie-Tooth neuropathy, type 2A1", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2A1", "Hereditary motor and sensory neuropathy 2 A", "hereditary motor and sensory neuropathy 2 A", "HEREDITARY MOTOR AND SENSORY NEUROPATHY IIA1", "hereditary motor and sensory neuropathy IIa1", "Hereditary Motor And Sensory Neuropathy IIA1", "hereditary motor and sensory neuropathy IIA1", "Charcot-Marie-Tooth disease, axonal, Type 2A", "Charcot-Marie-Tooth disease, axonal, type 2A", "Charcot-Marie-Tooth Disease, Axonal, Type 2a1", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A1", "Charcot-Marie-Tooth disease, axonal, type 2A1", "Charcot-Marie-Tooth disease neuronal type 2A1", "Charcot-Marie-Tooth disease, neuronal, Type 2A", "Charcot-Marie-Tooth disease, neuronal, type 2A", "Charcot-Marie-Tooth disease Type 2A (diagnosis)", "CHARCOT-MARIE-TOOTH DISEASE, NEURONAL, TYPE 2A1", "Charcot-Marie-Tooth disease, neuronal, type 2A1", "Charcot-Marie-Tooth Disease, Neuronal, Type 2a1", "Autosomal dominant Charcot-Marie-Tooth disease type 2A1", "autosomal dominant Charcot-Marie-Tooth disease type 2A1", "Charcot-Marie-Tooth disease type 2 caused by mutation in KIF1B", "autosomal dominant Charcot-Marie-Tooth disease axonal type 2A1", "Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2a1", "Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2A1", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A1", "Autosomal dominant Charcot-Marie-Tooth disease type 2A1 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 2A1", "shortest_name_length": 5}
{"curie": "UMLS:C0271673", "names": ["Symmetric diabetic proximal motor neuropathy", "Symmetric Diabetic Proximal Motor Neuropathy", "Symmetric proximal motor neuropathy with diabetes mellitus", "Symmetric proximal motor neuropathy due to diabetes mellitus", "Symmetric proximal motor neuropathy due to diabetes mellitus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Symmetric Diabetic Proximal Motor Neuropathy", "shortest_name_length": 44}
{"curie": "MONDO:0004769", "names": ["orbit; myositis", "myositis; orbit", "orbital myositis", "Orbital Myositis", "Orbital myositis", "myositis orbital", "Myositis, Orbital", "orbit pseudotumor", "pseudotumor; orbit", "orbit; pseudotumor", "Orbital Myositides", "orbital pseudotumor", "pseudotumor orbital", "Myositides, Orbital", "Orbital Pseudotumor", "Chronic pseudotumor", "Orbital pseudotumor", "pseudotumor, orbital", "Orbital Pseudotumors", "Orbital pseudotumour", "orbital pseudotumors", "Chronic pseudotumour", "Pseudotumor, Orbital", "Pseudotumor of orbit", "pseudotumor of orbit", "Pseudotumors, Orbital", "pseudotumors, orbital", "orbital pseudotumours", "Orbital myositis (disorder)", "orbital myositis (diagnosis)", "orbital plasma cell granuloma", "plasma cell granuloma, orbital", "orbital granuloma, plasma cell", "orbital pseudotumor (diagnosis)", "Idiopathic orbital inflammation", "granuloma, plasma cell, orbital", "Orbital Inflammatory Pseudotumor", "orbital inflammatory pseudotumor", "pseudotumor, orbital inflammatory", "inflammatory pseudotumor, orbital", "Inflammatory pseudotumor of orbit", "inflammatory pseudotumor of orbit", "Orbital Inflammatory Pseudotumors", "orbital inflammatory pseudotumors", "Pseudotumor, Orbital Inflammatory", "Inflammatory Pseudotumor, Orbital", "Inflammatory Pseudotumor of Orbit", "Pseudotumor, Inflammatory, Orbital", "inflammatory pseudotumors, orbital", "Inflammatory Pseudotumors, Orbital", "Inflammatory pseudotumour of orbit", "pseudotumor, inflammatory, orbital", "Pseudotumor (inflammatory) of orbit", "Inflammatory pseudotumor of orbit proper", "Inflammatory pseudotumour of orbit proper", "Inflammatory pseudotumor of orbit proper (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orbital plasma cell granuloma", "shortest_name_length": 15}
{"curie": "MONDO:0018250", "names": ["diffuse palmoplantar keratoderma with painful fissures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diffuse palmoplantar keratoderma with painful fissures", "shortest_name_length": 54}
{"curie": "MONDO:0001620", "names": ["lice; relapsing fever", "Louse-borne Relapsing Fever", "Louse-borne relapsing fever", "Louse borne Relapsing Fever", "louse-borne relapsing fever", "Louse-Borne Relapsing Fever", "Relapsing Fever, Louse-borne", "Louse-borne Relapsing Fevers", "Relapsing fever, louse-borne", "Fever, Louse-borne Relapsing", "febris; recurrens, louse-borne", "Borrelia recurrentis Infection", "Borrelia recurrentis infection", "disease (or disorder); Carapata", "Infection, Borrelia recurrentis", "Borrelia recurrentis Infections", "Louse-borne relapsing fever, NOS", "Louse-borne relapsing fever (disorder)", "louse-borne relapsing fever (diagnosis)", "Relapsing fever due to Borrelia recurrentis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "louse-borne relapsing fever", "shortest_name_length": 21}
{"curie": "UMLS:C0334334", "names": ["Adrenal Gland Clear Cell Adenoma", "Clear Cell Adrenocortical Adenoma", "Adrenal Cortex Clear Cell Adenoma", "Clear Cell Adrenal Cortex Adenoma", "Clear Cell Adrenal Cortical Adenoma", "Adrenal Cortical Clear Cell Adenoma", "Adrenal cortical adenoma, clear cell", "clear cell; adenoma, adrenal (cortex)", "Adrenal cortical adenoma - clear cell", "Adrenal cortical adenoma, clear cell type", "Adrenal cortical adenoma, clear cell (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clear Cell Adrenal Cortical Adenoma", "shortest_name_length": 32}
{"curie": "UMLS:C1333986", "names": ["Familial Female Breast Carcinoma", "Hereditary Female Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hereditary Female Breast Carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0018920", "names": ["PPCM", "Meadows' syndrome", "Puerperal cardiomyopathy", "cardiomyopathy peripartum", "Peripartum cardiomyopathy", "Postpartum cardiomyopathy", "CARDIOMYOPATHY POSTPARTUM", "peripartum cardiomyopathy", "postpartum cardiomyopathy", "cardiomyopathy postpartum", "Peripartum Cardiomyopathy", "cardiomyopathy; puerperal", "cardiomyopathy puerperium", "postpartum; cardiomyopathy", "cardiomyopathy; postpartum", "puerperium; cardiomyopathy", "Cardiomyopathy in the puerperium", "Postpartum cardiomyopathy (disorder)", "postpartum peripartum cardiomyopathy", "antepartum peripartum cardiomyopathy", "postpartum cardiomyopathy (diagnosis)", "Peripartum cardiomyopathy in puerperium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peripartum cardiomyopathy", "shortest_name_length": 4}
{"curie": "MONDO:0008484", "names": ["Teunissen-Cremers syndrome", "Teunissen-Cremers Syndrome", "TEUNISSEN-CREMERS SYNDROME", "Teunissen Cremers syndrome", "Stapes Ankylosis With Broad Thumb And Toes", "stapes ankylosis with BROAD thumb and toes", "stapes ankylosis with broad thumbs and toes", "STAPES ANKYLOSIS WITH BROAD THUMBS AND TOES", "Stapes ankylosis with broad thumbs and toes", "Stapes Ankylosis Syndrome Without Symphalangism", "STAPES ANKYLOSIS SYNDROME WITHOUT SYMPHALANGISM", "stapes ankylosis syndrome without symphalangism", "Stapes ankylosis with broad thumb and toe syndrome", "STAPES ANKYLOSIS WITH BROAD THUMB AND TOES (disorder)", "Stapes ankylosis with broad thumb and toe syndrome (disorder)", "ankylosis of stapes, hyperopia, Broad thumbs, Broad first toes, and syndactyly", "Ankylosis Of Stapes, Hyperopia, Broad Thumbs, Broad First Toes, And Syndactyly", "ANKYLOSIS OF STAPES, HYPEROPIA, BROAD THUMBS, BROAD FIRST TOES, AND SYNDACTYLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stapes ankylosis with broad thumbs and toes", "shortest_name_length": 26}
{"curie": "MONDO:0020122", "names": ["IIm", "IMM", "idiopathic inflammatory myositis", "idiopathic inflammatory myopathies", "acquired idiopathic inflammatory myopathy", "idiopathic inflammatory myopathy, familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired idiopathic inflammatory myopathy", "shortest_name_length": 3}
{"curie": "UMLS:C4528755", "names": ["Stage IIC Colon Cancer", "Stage IIC Colon Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIC Colon Cancer AJCC v8", "shortest_name_length": 22}
{"curie": "MONDO:0030819", "names": ["MKS14", "meckel syndrome 14", "MECKEL SYNDROME 14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "meckel syndrome 14", "shortest_name_length": 5}
{"curie": "MONDO:0010145", "names": ["tibia, absence of, with congenital deafness", "Tibia, Absence of, with Congenital Deafness", "TIBIA, ABSENCE OF, WITH CONGENITAL DEAFNESS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tibia, absence of, with congenital deafness", "shortest_name_length": 43}
{"curie": "MONDO:0021457", "names": ["Benign Pleural Tumor", "benign pleural tumor", "Benign Tumor of Pleura", "pleura benign neoplasm", "Benign tumor of pleura", "benign tumor of pleura", "Benign tumour of pleura", "Benign pleural neoplasm", "benign pleural neoplasm", "Benign Pleural Neoplasm", "Benign Neoplasm of Pleura", "Benign neoplasm of pleura", "benign neoplasm of pleura", "Benign Tumor of the Pleura", "benign tumor of the pleura", "benign neoplasm of the pleura", "Benign Neoplasm of the Pleura", "Benign neoplasm of pleura, NOS", "Benign neoplasm of pleura (disorder)", "benign neoplasm of pleura (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of pleura", "shortest_name_length": 20}
{"curie": "MONDO:0014433", "names": ["BBS4", "Bardet-Biedl syndrome 4", "BARDET-BIEDL SYNDROME 4", "Bardet-Biedl syndrome type 4", "Bardet-Biedl syndrome 4 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bardet-Biedl syndrome 4", "shortest_name_length": 4}
{"curie": "UMLS:C0751262", "names": ["Adult Learning Disorder", "Learning Disorder, Adult", "Adult Learning Disorders", "Disorders, Adult Learning", "Adult Learning Disability", "Learning Disorders, Adult", "Learning Disability, Adult", "Disability, Adult Learning", "Adult Learning Disabilities", "Disabilities, Adult Learning", "Learning Disabilities, Adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Learning Disabilities", "shortest_name_length": 23}
{"curie": "UMLS:C0751438", "names": ["Posterior", "Disorder of neurophysis", "Neurohypophyseal Disease", "Neurohypophysis disorder", "neurohypophysis; disorder", "Disease, Neurohypophyseal", "Neurohypophyseal Diseases", "Diseases, Neurohypophyseal", "Posterior Pituitary Disease", "posterior pituitary disease", "Posterior pituitary disease", "Disorder of neurohypophysis", "Pituitary Disease, Posterior", "Disease, Posterior Pituitary", "Posterior pituitary disorder", "Posterior Pituitary Diseases", "Diseases, Posterior Pituitary", "Pituitary Diseases, Posterior", "Posterior pituitary disorders", "posterior pituitary disorders", "Disease of posterior pituitary", "Disorder of posterior pituitary", "disorder of posterior pituitary", "Diseases of Posterior Pituitary", "Disorder of neurohypophysis, NOS", "Disorder of posterior pituitary, NOS", "disease (or disorder); neurohypophysis", "DISEASES OF THE POSTERIOR PITUITARY GLAND", "Disorder of posterior pituitary (disorder)", "disorder of posterior pituitary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Posterior pituitary disease", "shortest_name_length": 9}
{"curie": "UMLS:C0571818", "names": ["Iodine allergy", "IODINE ALLERGY", "iodine allergy", "allergy iodine", "allergies iodine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Iodine allergy", "shortest_name_length": 14}
{"curie": "UMLS:C4552932", "names": ["II", "Stage II Cervical Cancer", "Stage II Cervical Cancer AJCC v8", "Stage II Cervical Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Cervical Cancer AJCC v8", "shortest_name_length": 2}
{"curie": "MONDO:0014239", "names": ["TACHD", "TESTICULAR ANOMALIES WITH OR WITHOUT CONGENITAL HEART DISEASE", "testicular anomalies with or without congenital heart disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular anomalies with or without congenital heart disease", "shortest_name_length": 5}
{"curie": "MONDO:0100420", "names": ["AML, C-KIT Mutation", "AML, CD117 Mutation", "AML, KIT gene mutation", "AML, CD117 Gene Mutation", "AML, c-KIT Gene Mutation", "acute myeloid leukemia, KIT gene mutation", "AML, KIT Proto-Oncogene Tyrosine Protein Kinase Gene Mutation", "AML, V-Kit Hardy-Zuckerman 4 Feline Sarcoma Viral Oncogene Homolog Gene Mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, KIT gene mutation", "shortest_name_length": 19}
{"curie": "MONDO:0003308", "names": ["pleura mesothelioma", "pleura; mesothelioma", "PLEURAL MESOTHELIOMA", "Pleural Mesothelioma", "mesothelioma; pleura", "Pleural mesothelioma", "pleural mesothelioma", "Mesothelioma of Pleura", "Mesothelioma of pleura", "mesothelioma of pleura", "Pleural Adenomatoid Tumor", "mesothelioma of the pleura", "Mesothelioma of the Pleura", "Benign pleural mesothelioma", "pleura; benign mesothelioma", "Pleural mesothelioma benign", "Pleural Benign Mesothelioma", "benign pleural mesothelioma", "Pleural Mesothelioma, Benign", "pleura; mesothelioma, benign", "mesothelioma; benign, pleura", "PLEURA, MESOTHELIOMA, PRIMARY", "Benign mesothelioma of pleura", "benign mesothelioma of pleura", "Benign Mesothelioma of Pleura", "pleural mesothelioma (disease)", "Benign Mesothelioma of the Pleura", "pleural mesothelioma (disease), benign", "benign mesothelioma of pleura (diagnosis)", "Benign neoplasm of mesothelial tissue of pleura", "Benign neoplasm of mesothelial tissue of pleura (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pleural mesothelioma", "shortest_name_length": 19}
{"curie": "UMLS:C0020631", "names": ["familial hypophosphatemia", "Familial hypophosphatemia", "Familial Hypophosphatemia", "Familial hypophosphataemia", "Hypophosphatemia, Familial", "Familial Hypophosphatemias", "Hypophosphatemias, Familial", "familial hypophosphatemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Familial hypophosphatemia", "shortest_name_length": 25}
{"curie": "MONDO:0000242", "names": ["barber itch", "barber rash", "tinea barbae", "tinea; beard", "barbers rash", "Tinea Barbae", "Tinea barbae", "barbers itch", "beard; tinea", "Barbers' itch", "tinea; barbae", "Barbers' rash", "Tinea sycosis", "barbae; tinea", "barber's itch", "tinea; sycosis", "sycosis barbae", "Sycosis barbae", "Beard ringworm", "beard ringworm", "sycosis; tinea", "beard; ringworm", "ringworm; beard", "Mycotic sycosis", "mycotic sycosis", "mycotic; sycosis", "sycosis vulgaris", "Sycosis vulgaris", "sycosis; mycotic", "Sycosis, mycotic", "folliculitis barbae", "Folliculitis barbae", "beard dermatophytosis", "BEARD DERMATOPHYTOSIS", "beard; dermatophytosis", "dermatophytosis; beard", "Tinea barbae (disorder)", "dermatophytosis of beard", "Dermatophytosis of beard", "mycotic sycosis (diagnosis)", "Sycosis barbae, not parasitic", "dermatophytosis of beard (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tinea barbae", "shortest_name_length": 11}
{"curie": "MONDO:0007845", "names": ["MCD", "susceptibility to Kaposi sarcoma", "KAPOSI SARCOMA, SUSCEPTIBILITY TO", "Kaposi sarcoma, susceptibility to", "multicentric Castleman disease, susceptibility to", "MULTICENTRIC CASTLEMAN DISEASE, SUSCEPTIBILITY TO", "multiple idiopathic pigmented hemangiosarcoma, susceptibility to", "MULTIPLE IDIOPATHIC PIGMENTED HEMANGIOSARCOMA, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kaposi sarcoma, susceptibility to", "shortest_name_length": 3}
{"curie": "UMLS:C1335156", "names": ["Ovarian Dermoid Cyst with Secondary Tumor", "Somatic Neoplasm Arising from Ovarian Teratoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Dermoid Cyst with Secondary Tumor", "shortest_name_length": 41}
{"curie": "UMLS:C1512436", "names": ["High Grade Prostatic Intraepithelial Neoplasia, Inverted Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Prostatic Intraepithelial Neoplasia, Inverted Variant", "shortest_name_length": 64}
{"curie": "MONDO:0018869", "names": ["Lissencephaly type 2", "Type 2 lissencephaly", "Lissencephaly Type 2", "lissencephaly type 2", "Lissencephaly type II", "Cobblestone Dysplasia", "Type II lissencephaly", "Dysplasia, Cobblestone", "Cobblestone Dysplasias", "Dysplasias, Cobblestone", "Cobblestone lissencephaly", "Cobblestone Lissencephaly", "cobblestone lissencephaly", "Lissencephaly, Cobblestone", "Lissencephaly, cobblestone", "Cobblestone Lissencephalies", "Lissencephalies, Cobblestone", "Type 2 lissencephaly (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cobblestone lissencephaly", "shortest_name_length": 20}
{"curie": "MONDO:0009789", "names": ["Naion, susceptibility to", "NAION, SUSCEPTIBILITY TO", "optic neuropathy, anterior ischemic, susceptibility to", "OPTIC NEUROPATHY, ANTERIOR ISCHEMIC, SUSCEPTIBILITY TO", "susceptibility to nonarteritic anterior ischemic optic neuropathy", "nonarteritic anterior ischemic optic neuropathy, susceptibility to", "NONARTERITIC ANTERIOR ISCHEMIC OPTIC NEUROPATHY, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nonarteritic anterior ischemic optic neuropathy, susceptibility to", "shortest_name_length": 24}
{"curie": "MONDO:0010810", "names": ["VDDR1B", "vitamin D-dependent rickets type 1B", "vitamin D 25-Hydroxylase deficiency", "Vitamin D 25-Hydroxylase Deficiency", "VITAMIN D-DEPENDENT RICKETS, TYPE 1B", "Vitamin D-Dependent Rickets, Type 1B", "vitamin D-dependent rickets, type 1B", "25-HYDROXYVITAMIN D3 DEFICIENCY, SELECTIVE", "25-Hydroxyvitamin D3 deficiency, selective", "25-Hydroxyvitamin D3 Deficiency, Selective", "CYP2R1 vitamin D-dependent rickets, type 1", "Vitam D hydroxylation-deficient rickets type 1b", "Vitam D Hydroxylation-Deficient Rickets Type 1b", "vitamin D hydroxylation-deficient rickets type 1b", "Vitamin D Hydroxylation-deficient Rickets Type 1b", "VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B", "vitamin D hydroxylation-deficient rickets, type 1B", "Vitamin D Hydroxylation-Deficient Rickets, Type 1B", "rickets due to defect in vitamin D 25-hydroxylation deficiency", "vitamin D-dependent rickets, type 1 caused by mutation in CYP2R1", "PSEUDOVITAMIN D3 DEFICIENCY RICKETS DUE TO 25-HYDROXYLASE DEFICIENCY", "Pseudovitamin D3 deficiency rickets due to 25-Hydroxylase deficiency", "Pseudovitamin D3 Deficiency Rickets Due To 25-Hydroxylase Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitamin D hydroxylation-deficient rickets, type 1B", "shortest_name_length": 6}
{"curie": "UMLS:C4285814", "names": ["Tumefactive multiple sclerosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tumefactive multiple sclerosis", "shortest_name_length": 30}
{"curie": "MONDO:0013174", "names": ["CILD13", "primary ciliary dyskinesia 13", "CILIARY DYSKINESIA, PRIMARY, 13", "Ciliary Dyskinesia, Primary, 13", "ciliary dyskinesia, primary, 13", "DNAAF1 primary ciliary dyskinesia", "primary ciliary dyskinesia type 13", "ciliary dyskinesia, primary, type 13", "primary ciliary dyskinesia caused by mutation in DNAAF1", "primary ciliary dyskinesia 13 with or without situs inversus", "ciliary dyskinesia, primary, 13, with or without situs inversus", "CILIARY DYSKINESIA, PRIMARY, 13, WITH OR WITHOUT SITUS INVERSUS", "Ciliary Dyskinesia, Primary, 13, With Or Without Situs Inversus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia 13", "shortest_name_length": 6}
{"curie": "UMLS:C1334716", "names": ["Metastatic Carcinoma in the Adrenal Cortex", "Metastatic Carcinoma to the Adrenal Cortex"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Carcinoma in the Adrenal Cortex", "shortest_name_length": 42}
{"curie": "MONDO:0010863", "names": ["T1D5", "IDDM5", "TYPE 1 DIABETES MELLITUS 5", "type 1 diabetes mellitus 5", "SUMO4 type 1 diabetes mellitus", "insulin-dependent diabetes mellitus 5", "Insulin-Dependent Diabetes Mellitus 5", "INSULIN-DEPENDENT DIABETES MELLITUS 5", "DIABETES MELLITUS, INSULIN-DEPENDENT, 5", "Diabetes Mellitus, Insulin-Dependent, 5", "diabetes mellitus, insulin-dependent, 5", "diabetes mellitus, insulin-dependent, type 5", "type 1 diabetes mellitus caused by mutation in SUMO4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type 1 diabetes mellitus 5", "shortest_name_length": 4}
{"curie": "MONDO:0013743", "names": ["SLEB16", "familial SLE", "autosomal SLE", "SYSTEMIC LUPUS ERYTHEMATOSUS 16", "systemic lupus erythematosus 16", "systemic lupus erythematosus type 16", "familial systemic lupus erythematosus", "autosomal systemic lupus erythematosus type 16"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal systemic lupus erythematosus type 16", "shortest_name_length": 6}
{"curie": "MONDO:0012924", "names": ["DBA4", "DIAMOND-BLACKFAN ANEMIA 4", "Diamond-Blackfan anemia 4", "Diamond-Blackfan Anemia 4", "RPS17 Diamond-Blackfan anemia", "Diamond-Blackfan Anemia type 4", "RPS17-related Diamond-Blackfan anemia", "Diamond-Blackfan anemia caused by mutation in RPS17"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diamond-Blackfan anemia 4", "shortest_name_length": 4}
{"curie": "UMLS:C4329734", "names": ["Diffuse KATP-Associated Hyperinsulinism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse KATP-Associated Hyperinsulinism", "shortest_name_length": 39}
{"curie": "MONDO:0001161", "names": ["Schizoid Personality", "Schizoid personality", "schizoid personality", "Personality, Schizoid", "Schizoid Personalities", "Personalities, Schizoid", "PERSONALITY DISORDER SCHIZOID", "disorder personality schizoid", "Schizoid Personality Disorder", "schizoid personality disorder", "Schizoid personality disorder", "SCHIZOID PERSONALITY DISORDER", "Disorder, Schizoid Personality", "Personality Disorder, Schizoid", "schizoid; personality disorder", "schizoid personality disorders", "Schizoid Personality Disorders", "personality disorder; schizoid", "Personality Disorders, Schizoid", "Disorders, Schizoid Personality", "Schizoid personality disorder (disorder)", "schizoid personality disorder (diagnosis)", "Schizoid personality disorder, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schizoid personality disorder", "shortest_name_length": 20}
{"curie": "UMLS:C5555537", "names": ["PDST", "Periductal Stromal Tumor", "Breast Periductal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Periductal Stromal Tumor", "shortest_name_length": 4}
{"curie": "MONDO:0014033", "names": ["DYT25", "dystonia 25", "DYSTONIA 25", "Dystonia 25", "dystonia type 25", "GNAL dystonic disorder", "dystonic disorder caused by mutation in GNAL", "Autosomal dominant focal dystonia DYT25 type", "autosomal dominant focal dystonia, DYT25 type", "Autosomal dominant focal dystonia, DYT25 type", "Autosomal dominant focal dystonia DYT25 type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dystonia 25", "shortest_name_length": 5}
{"curie": "UMLS:C1335703", "names": ["Recurrent Head and Neck Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Head and Neck Carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0019551", "names": ["CMT6", "HMSN6", "CMT6A", "HMSN 6", "HMSN6A", "HMSN VI", "HMSN VIA", "Charcot-Marie-Tooth disease type 6", "CHARCOT-MARIE-TOOTH DISEASE, TYPE 6", "Charcot-Marie-Tooth Disease, Type 6", "CHARCOT-MARIE-TOOTH DISEASE, TYPE 6A", "Peripheral neuropathy and optic atrophy", "Peripheral Neuropathy And Optic Atrophy", "peripheral neuropathy and optic atrophy", "PERIPHERAL NEUROPATHY AND OPTIC ATROPHY", "Hereditary Motor And Sensory Neuropathy VI", "Hereditary sensory-motor neuropathy, type 6", "Hereditary motor-sensory neuropathy, type VI", "Hereditary motor and sensory neuropathy type 6", "hereditary motor and sensory neuropathy type 6", "Hereditary motor and sensory neuropathy type VI", "Hereditary sensory and motor neuropathy, type VI", "NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VI", "NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIA", "Hereditary motor-sensory neuropathy with optic atrophy", "Hereditary motor and sensory neuropathy with optic atrophy", "hereditary motor and sensory neuropathy with optic atrophy", "Hereditary sensory-motor neuropathy, type 6 with optic atrophy", "Hereditary motor and sensory neuropathy with optic atrophy (disorder)", "hereditary motor and sensory neuropathy with optic atrophy (diagnosis)", "NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIA, WITH OPTIC ATROPHY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary motor and sensory neuropathy type 6", "shortest_name_length": 4}
{"curie": "UMLS:C0948050", "names": ["Small bowel angioedema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small bowel angioedema", "shortest_name_length": 22}
{"curie": "UMLS:C2986705", "names": ["Erythroleukoplakia", "erythroleukoplakia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Erythroleukoplakia", "shortest_name_length": 18}
{"curie": "MONDO:0018667", "names": ["empyema", "pyothorax", "PYOTHORAX", "Pyothorax", "lung empyema", "chest empyema", "Empyema, lung", "empyema chest", "thorax abscess", "Empyema, chest", "empyema pleura", "abscess; chest", "chest; abscess", "Thorax abscess", "EMPYEMA OF LUNG", "thorax; abscess", "Pleural Empyema", "pleural empyema", "empyema of lung", "Empyema, pleura", "empyema pleural", "Pleural empyema", "abscess; thorax", "Abscess, thorax", "Empyema thoracis", "thoracic empyema", "thoracic abscess", "Empyema, Pleural", "Pleural Empyemas", "Thoracic Empyema", "Empyema of pleura", "abscess of thorax", "Empyema, Thoracic", "Empyemas, Pleural", "empyema of pleura", "Pulmonary Empyema", "purulent pleurisy", "pulmonary empyema", "Purulent pleurisy", "EMPYEMA, THORACIC", "Pulmonary empyema", "Thoracic Empyemas", "Abscess of thorax", "Pleurisy, purulent", "Empyemas, Thoracic", "pleurisy; purulent", "purulent; pleurisy", "purulent pleuritis", "PLEURITIS, PURULENT", "empyema with fistula", "Suppurative pleurisy", "Pleurisy, suppurative", "pleurisy; suppurative", "suppurative; pleurisy", "Empyema of pleura, NOS", "Empyema with no fistula", "pleural empyema (disease)", "abscess of pleural cavity", "Abscess of pleural cavity", "Empyema of pleura (disorder)", "Abscess of thorax (disorder)", "thoracic empyema (diagnosis)", "Pleural empyema with fistula", "Empyema with pleural fistula", "Abscess of thorax (diagnosis)", "empyema of pleura (diagnosis)", "thoracic abscess pleural cavity", "pleural empyema with no fistula", "Empyema of pleura without fistula", "Empyema without mention of fistula", "Abscess of pleural cavity (disorder)", "Abscess of pleural cavity (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pleural empyema", "shortest_name_length": 7}
{"curie": "UMLS:C4744308", "names": ["Recurrent Extremity Sarcoma", "Recurrent Sarcoma of the Extremity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Sarcoma of the Extremity", "shortest_name_length": 27}
{"curie": "UMLS:C1336361", "names": ["Stage IVB Lip Basal Cell Cancer", "Stage IVB Basal Cell Lip Carcinoma", "Stage IVB Basal Cell Carcinoma of Lip", "stage IVB basal cell carcinoma of the lip", "Stage IVB Basal Cell Carcinoma of the Lip"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Basal Cell Lip Carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0004155", "names": ["adult CNS embryonal carcinoma", "Adult CNS Embryonal Carcinoma", "Embryonal Carcinoma of Adult CNS", "embryonal carcinoma of adult CNS", "embryonal carcinoma of the adult CNS", "Embryonal Carcinoma of the Adult CNS", "Central nervous system embryonal carcinoma", "Central Nervous System Embryonal Carcinoma", "adult central nervous system embryonal carcinoma", "Adult Central Nervous System Embryonal Carcinoma", "embryonal carcinoma of adult central nervous system", "Embryonal Carcinoma of Adult Central Nervous System", "Embryonal Carcinoma of the Adult Central Nervous System", "embryonal carcinoma of the adult central nervous system", "Embryonal carcinoma of the adult central nervous system", "adult embryonal carcinoma of the central nervous system", "embryonal carcinoma of the central nervous system of adults"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult central nervous system embryonal carcinoma", "shortest_name_length": 29}
{"curie": "UMLS:C4086166", "names": ["Nongerminomatous Germ Cell Tumor", "Childhood Nongerminomatous Germ Cell Tumor", "Childhood Non-Germinomatous Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Nongerminomatous Germ Cell Tumor", "shortest_name_length": 32}
{"curie": "UMLS:C1332941", "names": ["childhood AMOL", "pediatric AMOL", "AMOL, pediatric", "AMOL, childhood", "M5 childhood AMOL", "pediatric acute monocytic leukemia", "acute monocytic leukemia, childhood", "monocytic leukemia, childhood acute", "leukemia, childhood acute monocytic", "M5 childhood acute monocytic leukemia", "M5 pediatric acute monocytic leukemia", "childhood acute monocytic leukemia (M5)", "Acute Monoblastic and Monocytic Leukemia", "Childhood Acute Monoblastic and Monocytic Leukemia", "Childhood Acute Monoblastic and Monocytic Leukemia (M5)", "childhood acute monoblastic and monocytic leukemia (M5)", "childhood acute monoblastic leukemia and monocytic leukemia", "childhood acute monoblastic leukemia and monocytic leukemia (M5)", "Childhood Acute Monoblastic Leukemia and Acute Monocytic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Acute Monoblastic and Monocytic Leukemia", "shortest_name_length": 14}
{"curie": "MONDO:0017626", "names": ["familial primary hypomagnesemia with normocalcuria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial primary hypomagnesemia with normocalcuria", "shortest_name_length": 50}
{"curie": "UMLS:C0751446", "names": ["Nonpoliovirus Poliomyelitis", "Poliomyelitis, Nonpoliovirus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Poliomyelitis, Nonpoliovirus", "shortest_name_length": 27}
{"curie": "MONDO:0021327", "names": ["Urethral Ca", "Urethra cancer", "URETHRA CANCER", "urethra cancer", "Urethra Cancer", "cancer urethra", "urethral cancer", "Cancer, Urethra", "Urethral cancer", "Urethra Cancers", "Urethral Cancer", "Urethral Cancers", "Cancers, Urethra", "Cancer, Urethral", "Urethra Carcinoma", "Carcinoma;urethra", "Cancer of Urethra", "Cancers, Urethral", "carcinoma urethra", "cancer of urethra", "urethra carcinoma", "urethral carcinoma", "URETHRA, CARCINOMA", "Urethral Carcinoma", "Urethral cancer NOS", "carcinoma of urethra", "Carcinoma of urethra", "Carcinoma of Urethra", "cancer of the urethra", "Cancer of the Urethra", "CA - Cancer of urethra", "Carcinoma of the Urethra", "carcinoma of the urethra", "URETHRAL CANCER, CARCINOMA", "urethral carcinoma (diagnosis)", "carcinoma of urethra (diagnosis)", "Malignant epithelial neoplasm of urethra", "Malignant epithelial neoplasm of urethra (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma of urethra", "shortest_name_length": 11}
{"curie": "UMLS:C5206655", "names": ["Metastatic Merkel Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Merkel Cell Carcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C0149524", "names": ["PROSTATITIS ACUTE", "Acute Prostatitis", "prostatitis acute", "Acute prostatitis", "acute prostatitis", "acute; prostatitis", "PROSTATITIS, ACUTE", "prostatitis; acute", "Acute prostatitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute prostatitis", "shortest_name_length": 17}
{"curie": "MONDO:0015530", "names": ["trigeminal autonomic cephalgia", "Trigeminal autonomic cephalgia", "Trigeminal Autonomic Cephalalgia", "Trigeminal autonomic cephalalgia", "trigeminal autonomic cephalalgia", "Cephalalgia, Trigeminal Autonomic", "Trigeminal Autonomic Cephalalgias", "Cephalalgias, Trigeminal Autonomic", "trigeminal autonomic cephalgia (diagnosis)", "Trigeminal autonomic cephalalgia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trigeminal autonomic cephalalgia", "shortest_name_length": 30}
{"curie": "UMLS:C4683751", "names": ["Stage IVB Mycosis Fungoides and Sezary Syndrome AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Mycosis Fungoides and Sezary Syndrome AJCC v8", "shortest_name_length": 55}
{"curie": "UMLS:C1332305", "names": ["Anterior Tongue Mucoepidermoid Carcinoma", "Mucoepidermoid Carcinoma of Anterior Tongue", "Mucoepidermoid Carcinoma of the Anterior Tongue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anterior Tongue Mucoepidermoid Carcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0100205", "names": ["infection due to parainfluenza virus 4", "human rubulavirus 4 infectious disease", "infection caused by parainfluenza virus 4", "infection due to human parainfluenza virus 4", "parainfluenza virus type 4 infectious disease", "infection caused by human parainfluenza virus 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parainfluenza virus type 4 infectious disease", "shortest_name_length": 38}
{"curie": "UMLS:C0342347", "names": ["Parathyroid cyst", "Parathyroid Cyst", "parathyroid cyst", "cyst parathyroid", "cysts parathyroid", "parathyroid; cyst", "cyst; parathyroid", "Cyst of parathyroid", "Cyst of Parathyroid", "parathyroid gland cyst", "Cyst of the Parathyroid", "Cyst of parathyroid gland", "Cyst of parathyroid (disorder)", "parathyroid gland cyst (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cyst of parathyroid", "shortest_name_length": 16}
{"curie": "MONDO:0015073", "names": ["gallbladder NET", "Gallbladder NET", "Gallbladder Neuroendocrine Tumor", "gallbladder neuroendocrine tumor", "gallbladder neuroendocrine tumor, grade 1/2", "gallbladder well differentiated endocrine tumor", "Gallbladder Well Differentiated Endocrine Tumor", "gallbladder well differentiated endocrine tumor/carcinoma", "Gallbladder Well Differentiated Endocrine Tumor/Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gallbladder neuroendocrine tumor, grade 1/2", "shortest_name_length": 15}
{"curie": "MONDO:0018901", "names": ["LVNC", "spongy myocardium", "Spongy myocardium", "Lv non-compaction syndrome", "LV Non-Compaction Syndrome", "Left ventricular noncompaction", "left ventricular noncompaction", "left ventricular hypertrabeculation", "Left ventricular hypertrabeculation", "left ventricular non-compaction syndrome", "left ventricular noncompaction (disease)", "Left Ventricular Non-Compaction Syndrome", "left ventricular non-compaction cardiomyopathy", "Left Ventricular Non-Compaction Cardiomyopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "left ventricular noncompaction", "shortest_name_length": 4}
{"curie": "MONDO:0018098", "names": ["LGMD1E", "LGMD1D, FORMERLY", "limb-girdle muscular dystrophy type 1E", "Muscular Dystrophy, Limb-Girdle, Type 1E", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1E", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1D, FORMERLY", "autosomal dominant limb-girdle muscular dystrophy type 1E (DES)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant limb-girdle muscular dystrophy type 1E (DES)", "shortest_name_length": 6}
{"curie": "UMLS:C4329651", "names": ["Cervical Spinal Cord Ependymal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Spinal Cord Ependymal Tumor", "shortest_name_length": 36}
{"curie": "UMLS:C4553671", "names": ["Stage IIIA Fallopian Tube Cancer", "Stage IIIA Fallopian Tube Cancer AJCC v8", "Stage IIIA Fallopian Tube Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Fallopian Tube Cancer AJCC v8", "shortest_name_length": 32}
{"curie": "UMLS:C5670614", "names": ["Embryonal Tumor with Multilayered Rosettes, DICER1-Mutated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Embryonal Tumor with Multilayered Rosettes, DICER1-Mutated", "shortest_name_length": 58}
{"curie": "UMLS:C0278560", "names": ["stage II esophageal cancer", "Stage II Esophageal Cancer", "esophagus cancer, stage II", "esophageal cancer, stage II", "stage II cancer of the esophagus", "Stage II Esophageal Cancer AJCC v6", "Esophageal Cancer Stage II AJCC v6", "Stage II Esophagus Carcinoma AJCC v6", "Stage II Esophageal Carcinoma AJCC v6", "Stage II Carcinoma of Esophagus AJCC v6", "Stage II Carcinoma of the Esophagus AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Esophageal Cancer", "shortest_name_length": 26}
{"curie": "MONDO:0008248", "names": ["Schamberg purpura", "pigmented purpura", "Schamberg disease", "Familial capillaritis", "Gougerot-Blum capillaritis", "Gougerot and Blum syndrome", "PIGMENTED PURPURIC ERUPTION", "Pigmented purpuric eruption", "pigmented purpuric eruption", "Familial Schamberg's disease", "progressive pigmented purpura", "Pigmented purpuric dermatosis", "pigmented purpuric dermatosis", "Gougerot's trisymptomatic disease", "familial pigmented purpuric eruption", "Familial pigmented purpuric eruption", "pigmented purpuric lichenoid dermatitis", "Pigmented purpuric lichenoid dermatitis", "Familial pigmented purpuric eruption (disorder)", "pigmented purpuric lichenoid dermatitis of Gougerot-Blum", "Pigmented purpuric lichenoid dermatosis of Gougerot and Blum", "Pigmented purpuric lichenoid dermatitis of Gougerot and Blum", "pigmented purpuric lichenoid dermatitis of Gougerot-Blum (diagnosis)", "Pigmented purpuric lichenoid dermatitis of Gougerot and Blum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pigmented purpuric eruption", "shortest_name_length": 17}
{"curie": "UMLS:C0750920", "names": ["Post-Traumatic Aphasia", "Aphasia, Post Traumatic", "Aphasia, Post-Traumatic", "Post-Traumatic Aphasias"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aphasia, Post-Traumatic", "shortest_name_length": 22}
{"curie": "MONDO:0021161", "names": ["prostatitis gonococcal", "Prostatitis gonococcal", "Gonococcal prostatitis", "gonococcal prostatitis", "Gonococcal prostatitis (disorder)", "Gonococcal prostatitis (diagnosis)", "Neisseria gonorrhoeae prostatitis (disease)", "Neisseria gonorrhoeae caused prostatitis (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gonococcal prostatitis", "shortest_name_length": 22}
{"curie": "MONDO:0013291", "names": ["GSD15", "GSD XV", "GSD 15", "GSD type 15", "GSD type XV", "Gyg1 deficiency", "glycogenosis type 15", "Glycogenosis type 15", "Glycogenosis type XV", "glycogenosis type XV", "glycogenin deficiency", "GLYCOGENIN DEFICIENCY", "glycogen storage disease 15", "glycogen storage disease XV", "GLYCOGEN STORAGE DISEASE XV", "Glycogen storage disease 15", "glycogen storage disease type XV", "glycogen storage disease type 15", "Glycogen storage disease type 15", "Glycogen storage disease type XV", "GSD with severe cardiomyopathy due to glycogenin deficiency", "Glycogenosis with severe cardiomyopathy due to glycogenin deficiency", "glycogenosis with severe cardiomyopathy due to glycogenin deficiency", "glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency", "Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency", "Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease XV", "shortest_name_length": 5}
{"curie": "MONDO:0045057", "names": ["deliria", "Deliria", "delirium", "DELIRIUM", "Delirium", "Delirious", "delirious", "Delirium NOS", "OBS syndrome", "Delirium, NOS", "acute delirium", "DELIRIUM ACUTE", "Acute delirium", "Acute confusion", "acute confusion", "Acute Confusion", "delirium (symptom)", "Delirious (finding)", "Delirium (disorder)", "SYNDROME BRAIN ACUTE", "acute brain syndrome", "ACUTE BRAIN SYNDROME", "Acute brain syndrome", "Syndrome brain acute", "BRAIN SYNDROME ACUTE", "Unspecified delirium", "Brain syndrome acute", "Acute confusion state", "Delirium, unspecified", "Organic Brain Syndrome", "organic brain syndrome", "ORGANIC BRAIN SYNDROME", "Acute organic reaction", "Organic brain syndrome", "brain organic syndrome", "organic brain syndromes", "acute confusional state", "Acute confusional state", "Organic Brain Syndromes", "acute confusional states", "syndrome; brain, organic", "brain; syndrome, organic", "Acute confusion (finding)", "Acute brain syndrome, NOS", "ABS - Acute brain syndrome", "Organic brain syndrome NOS", "Organic brain syndrome, NOS", "OBS - Organic brain syndrome", "Acute psycho-organic syndrome", "delirium confusional state acute", "Acute confusional state (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "delirium", "shortest_name_length": 7}
{"curie": "UMLS:C0431593", "names": ["Intrahepatic Biliary Atresia", "Intrahepatic biliary atresia", "Congenital Intrahepatic Biliary Atresia", "Intrahepatic biliary atresia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Intrahepatic Biliary Atresia", "shortest_name_length": 28}
{"curie": "UMLS:C4743984", "names": ["Sickle Cell Chronic Lung Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sickle Cell Chronic Lung Disease", "shortest_name_length": 32}
{"curie": "MONDO:0032935", "names": ["RLSDF", "rhizomelic limb shortening with dysmorphic features", "RHIZOMELIC LIMB SHORTENING WITH DYSMORPHIC FEATURES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rhizomelic limb shortening with dysmorphic features", "shortest_name_length": 5}
{"curie": "MONDO:0009460", "names": ["Indolylacroyl Glycinuria with Mental Retardation", "INDOLYLACROYL GLYCINURIA WITH MENTAL RETARDATION", "indolylacroyl glycinuria with mental retardation", "indolylacroyl glycinuria with intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "indolylacroyl glycinuria with intellectual disability", "shortest_name_length": 48}
{"curie": "UMLS:C4682692", "names": ["Penile Cancer by AJCC v8 Stage", "Penile Squamous Cell Carcinoma by AJCC v8 Stage", "Squamous Cell Carcinoma of the Penis by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Penile Cancer by AJCC v8 Stage", "shortest_name_length": 30}
{"curie": "MONDO:0024279", "names": ["Chronic Endometritis", "Chronic endometritis", "chronic endometritis", "ENDOMETRITIS CHRONIC", "endometritis, chronic", "ENDOMETRITIS, CHRONIC", "chronic; endometritis", "endometritis; chronic", "Chronic endometritis (disorder)", "chronic endometritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic endometritis", "shortest_name_length": 20}
{"curie": "MONDO:0700168", "names": ["canine oral melanoma", "Canine Oral Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canine oral melanoma", "shortest_name_length": 20}
{"curie": "OMIM:609070", "names": ["HALAH", "HEMOGLOBIN, HIGH ALTITUDE ADAPTATION", "HEMOGLOBIN, HIGH OXYGEN SATURATION OF", "HEMOGLOBIN, HIGH ALTITUDE ADAPTATION PHENOTYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 5}
{"curie": "UMLS:C4724161", "names": ["Metastatic Fallopian Tube Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Fallopian Tube Carcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C0341851", "names": ["Vulvar Condyloma", "Vulvar Condyloma Acuminatum", "vulvar condyloma acuminatum", "Condyloma acuminata of vulva", "condyloma acuminatum of vulva", "Condylomata Acuminata of Vulva", "Condylomata Acuminata of the Vulva", "Condyloma acuminata of vulva (disorder)", "condyloma acuminatum of vulva (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Condyloma acuminata of vulva", "shortest_name_length": 16}
{"curie": "UMLS:C1168205", "names": ["Stage IVA Liver Cancer", "Hepatic cancer stage IVA", "Stage IVA Liver Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatic cancer stage IVA", "shortest_name_length": 22}
{"curie": "MONDO:0017523", "names": ["preaxial polydactyly type 1, unilateral", "polydactyly of a biphalangeal thumb, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polydactyly of a biphalangeal thumb, unilateral", "shortest_name_length": 39}
{"curie": "MONDO:0032625", "names": ["MC1DN21", "nuclear type mitochondrial complex I deficiency 21", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 21", "mitochondrial complex 1 deficiency, nuclear type 21"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 21", "shortest_name_length": 7}
{"curie": "MONDO:0001392", "names": ["monocular exotropia", "Monocular exotropia", "Monocular Exotropia", "Exotropia, Monocular", "Exotropia, monocular", "Monocular exotropia, NOS", "Monocular exotropia (disorder)", "monocular exotropia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "monocular exotropia", "shortest_name_length": 19}
{"curie": "UMLS:C0279097", "names": ["Childhood ALL in Remission", "pediatric ALL in remission", "childhood ALL in remission", "Pediatric ALL in Remission", "ALL in remission, childhood", "Childhood Acute Lymphoid Leukemia in Remission", "Pediatric Acute Lymphoid Leukemia in Remission", "Acute Lymphoblastic Leukemia (ALL) in Remission", "leukemia in remission, childhood acute leukemia", "remission, childhood acute lymphocytic leukemia", "Childhood Acute Lymphocytic Leukemia in Remission", "childhood acute lymphocytic leukemia in remission", "pediatric acute lymphocytic leukemia in remission", "Pediatric Acute Lymphocytic Leukemia in Remission", "acute lymphocytic leukemia in remission, childhood", "Childhood Acute Lymphogenous Leukemia in Remission", "Pediatric Acute Lymphogenous Leukemia in Remission", "lymphocytic leukemia in remission, childhood acute", "Childhood Acute Lymphoblastic Leukemia in Remission", "Pediatric Acute Lymphoblastic Leukemia in Remission", "childhood acute lymphoblastic leukemia in remission", "Childhood Precursor Lymphoblastic Leukemia in Remission"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Acute Lymphoblastic Leukemia in Remission", "shortest_name_length": 26}
{"curie": "MONDO:0012478", "names": ["OFC9", "OROFACIAL CLEFT 9", "Orofacial Cleft 9", "orofacial cleft 9", "nonsyndromic cleft lip with or without cleft palate 9", "cleft lip with or without cleft palate, nonsyndromic, 9", "CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 9", "Cleft Lip with or without Cleft Palate, Nonsyndromic, 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orofacial cleft 9", "shortest_name_length": 4}
{"curie": "MONDO:0003759", "names": ["pediatric Ovarian Yolk Sac tumor", "pediatric ovarian yolk Sac tumor", "Childhood Ovarian Yolk Sac Tumor", "Pediatric Ovarian Yolk Sac Tumor", "childhood ovarian yolk sac tumor", "childhood ovarian yolk sac tumour", "paediatric Ovarian Yolk Sac tumour", "pediatric ovarian yolk Sac neoplasm", "Pediatric Ovarian Yolk Sac Neoplasm", "Childhood Ovarian Yolk Sac Neoplasm", "childhood ovarian yolk Sac neoplasm", "ovary childhood endodermal sinus tumor", "pediatric ovarian endodermal sinus tumor", "childhood ovarian endodermal sinus tumor", "Childhood Ovarian Endodermal Sinus Tumor", "Pediatric Ovarian Endodermal Sinus Tumor", "childhood ovarian endodermal sinus tumour", "Pediatric Ovarian Endodermal Sinus Neoplasm", "pediatric ovarian endodermal sinus neoplasm", "Childhood Ovarian Endodermal Sinus Neoplasm", "childhood ovarian endodermal sinus neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood ovarian yolk sac tumor", "shortest_name_length": 32}
{"curie": "MONDO:0006298", "names": ["thymic malignant germ cell tumor", "Thymic Malignant Germ Cell Tumor", "malignant mediastinal germ cell tumor", "Mediastinal Malignant Germ Cell Tumor", "mediastinal malignant germ cell tumor", "Malignant Mediastinal Germ Cell Tumor", "mediastinal germ cell tumor, malignant", "malignant mediastinal germ cell neoplasm", "malignant germ cell tumor of mediastinum", "Malignant Mediastinal Germ Cell Neoplasm", "mediastinal neoplasm malignant germ cell", "Malignant Germ Cell Tumor of Mediastinum", "Malignant germ cell neoplasm of mediastinum", "malignant germ cell neoplasm of mediastinum", "Malignant Germ Cell Neoplasm of Mediastinum", "Malignant Germ Cell Tumor of the Mediastinum", "malignant germ cell tumor of the mediastinum", "Malignant Germ Cell Neoplasm of the Mediastinum", "malignant germ cell neoplasm of the mediastinum", "Malignant germ cell neoplasm of mediastinum (disorder)", "malignant germ cell neoplasm of mediastinum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mediastinal malignant germ cell tumor", "shortest_name_length": 32}
{"curie": "UMLS:C0151491", "names": ["MUSCULOSKELETAL ANOMALY", "anomaly; musculoskeletal", "musculoskeletal; anomaly", "Congenital anomaly;musculo", "Musculoskeletal Abnormality", "Abnormality, Musculoskeletal", "Musculoskeletal Abnormalities", "Abnormalities, Musculoskeletal", "Congenital Musculoskeletal Defect", "CONGENITAL MUSCULOSKELETAL ABNORM", "Musculoskeletal congenital anomaly", "Congenital anomaly musculoskeletal", "Congenital musculoskeletal anomaly", "MUSCULOSKELETAL CONGENITAL ANOMALY", "congenital musculoskeletal anomaly", "congenital musculoskeletal deformity", "Congenital musculoskeletal anomalies", "musculoskeletal; deformity, congenital", "Congenital musculoskeletal abnormality", "ANOMALY CONGENITAL MUSCULOSKELETAL (NOS)", "Anomaly congenital musculoskeletal (NOS)", "Congenital musculoskeletal abnormality NOS", "Congenital musculoskeletal abnormality, NOS", "Congenital anomaly of musculoskeletal system", "deformity; musculoskeletal system, congenital", "Congenital deformity of musculoskeletal system", "congenital malformations musculoskeletal system", "congenital musculoskeletal deformity (diagnosis)", "Congenital abnormality of musculoskeletal system", "Congenital anomaly of musculoskeletal system NOS", "congenital anomaly of the musculoskeletal system", "Congenital anomaly of musculoskeletal system, NOS", "Congenital malformation of musculoskeletal system", "Congenital deformity of musculoskeletal system NOS", "congenital malformations of musculoskeletal system", "CONGENITAL ANOMALIES OF THE MUSCULOSKELETAL SYSTEM", "Congenital deformity of musculoskeletal system, NOS", "Congenital Abnormality of the Musculoskeletal System", "Congenital anomaly of musculoskeletal system (disorder)", "Congenital malformation of musculoskeletal system, unspecified", "congenital malformations of musculoskeletal system (diagnosis)", "CONGENITAL ANOMALIES OF THE MUSCULOSKELETAL SYSTEM: GENERAL TERMS", "Congenital malformation and deformation of the musculoskeletal system", "Congenital malformations and deformations of the musculoskeletal system", "Congenital malformations and deformations of the musculoskeletal system (Q65-Q79)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital musculoskeletal anomalies", "shortest_name_length": 23}
{"curie": "MONDO:0018495", "names": ["X-linked intellectual disability-limb spasticity-retinal dystrophy-diabetes insipidus syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability-limb spasticity-retinal dystrophy-diabetes insipidus syndrome", "shortest_name_length": 94}
{"curie": "MONDO:0003009", "names": ["Aldosteronism", "aldosteronism", "ALDOSTERONISM", "Cushing syndrome", "Aldosteronism NOS", "Aldosteronism, NOS", "Cushing's syndrome", "Hyperaldosteronism", "hyperaldosteronism", "HYPERALDOSTERONISM", "Hyperaldosteronaemia", "Increased aldosterone", "Hyperaldosteronism NOS", "Hyperaldosteronism, NOS", "Mineralocorticoid excess", "Aldosteronism (disorder)", "aldosteronism (diagnosis)", "primary hyperaldosteronism", "Elevated plasma aldosterone", "Hyperaldosteronism, unspecified", "Increased aldosterone production"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperaldosteronism", "shortest_name_length": 13}
{"curie": "MONDO:0017568", "names": ["acrodysplasia scoliosis", "Acrodysplasia scoliosis", "Prata Liberal Goncalves syndrome", "Prata Libéral Gonçalves syndrome", "Prata-Liberal-Goncalves syndrome", "Acrodysplasia scoliosis (disorder)", "brachydactyly-scoliosis-carpal fusion syndrome", "Brachydactyly-scoliosis-carpal fusion syndrome", "Brachydactyly, scoliosis, carpal fusion syndrome", "Brachydactyly, scoliosis, spina bifida occulta, and carpal synostosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prata-Liberal-Goncalves syndrome", "shortest_name_length": 23}
{"curie": "UMLS:C4540602", "names": ["PITUITARY ADENOMA 3, GROWTH HORMONE-SECRETING, SOMATIC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PITUITARY ADENOMA 3, GROWTH HORMONE-SECRETING, SOMATIC", "shortest_name_length": 54}
{"curie": "UMLS:C3203465", "names": ["Retinal perivascular sheathing"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retinal perivascular sheathing", "shortest_name_length": 30}
{"curie": "UMLS:C0334283", "names": ["Malignant gastrinoma", "malignant gastrinoma", "Gastrinoma malignant", "Malignant Gastrinoma", "Gastrinoma, malignant", "Malignant G cell tumor", "Malignant G cell tumour", "G cell tumor, malignant", "G cell tumour, malignant", "Gastrin cell tumor, malignant", "Gastrin cell tumour, malignant", "malignant gastrinoma (diagnosis)", "gastrinoma; malignant, unspecified site", "malignant; gastrinoma, unspecified site", "tumor; G cell, malignant, unspecified site", "G cell; tumor, malignant, unspecified site", "Gastrinoma, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrinoma, malignant", "shortest_name_length": 20}
{"curie": "MONDO:0015706", "names": ["mosaic trisomy 1", "trisomy 1 mosaicism", "Mosaic trisomy type 1", "Mosaic trisomy chromosome 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mosaic trisomy 1", "shortest_name_length": 16}
{"curie": "MONDO:0016803", "names": ["unspecified mitochondrial disorder", "unspecified inborn mitochondrial disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "unspecified inborn mitochondrial disorder", "shortest_name_length": 34}
{"curie": "MONDO:0020629", "names": ["MGRISCE", "microcephaly, growth restriction and increased sister chromatid exchange"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly, growth restriction and increased sister chromatid exchange", "shortest_name_length": 7}
{"curie": "MONDO:0060502", "names": ["NDMSBA", "PLAAND", "PLAA-associated neurodevelopmental disorder", "Phospholipase A2 activating protein-associated neurodevelopmental disorder", "PLAAND - phospholipase A2 activating protein-associated neurodevelopmental disorder", "Phospholipase A2 activating protein-associated neurodevelopmental disorder (disorder)", "NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES", "neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies", "shortest_name_length": 6}
{"curie": "UMLS:C1336714", "names": ["Mixed Choriocarcinoma and Teratoma of Testis", "Testicular Mixed Choriocarcinoma and Teratoma", "Mixed Choriocarcinoma and Teratoma of the Testis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular Mixed Choriocarcinoma and Teratoma", "shortest_name_length": 44}
{"curie": "UMLS:C1880480", "names": ["Ectopic Atrial Rhythm", "ECTOPIC ATRIAL RHYTHM", "Ectopic Supraventricular Rhythm", "Ectopic Atrial Rhythm by EKG Finding", "Ectopic Atrial Rhythm by ECG Finding"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ectopic Atrial Rhythm by ECG Finding", "shortest_name_length": 21}
{"curie": "EFO:0009705", "names": ["small intestine enteropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small intestine enteropathy", "shortest_name_length": 27}
{"curie": "MONDO:0002327", "names": ["intracranial cavernoma", "intracranial Cavernoma", "Intracranial Cavernoma", "Intracranial Cavernous Angioma", "intracranial cavernous angioma", "Intracranial Cavernous Hemangioma", "intracranial cavernous hemangioma", "cavernous hemangioma intracranial", "Intracranial cavernous hemangioma", "Intracranial cavernous haemangioma", "Intracranial cavernous hemangioma (disorder)", "Intracranial cavernous hemangioma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intracranial cavernous angioma", "shortest_name_length": 22}
{"curie": "MONDO:0008282", "names": ["POLYPOSIS, INTESTINAL, WITH MULTIPLE EXOSTOSES", "polyposis, intestinal, with multiple exostoses", "Polyposis, Intestinal, With Multiple Exostoses"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyposis, intestinal, with multiple exostoses", "shortest_name_length": 46}
{"curie": "MONDO:0020321", "names": ["AUL", "leukemia stem cell", "Stem Cell Leukemia", "Stem cell leukemia", "stem cell leukemia", "Leukemia Stem Cell", "Acute leukemia, NOS", "Acute Leukemia, NOS", "stem cell acute leukemia", "Stem Cell Acute Leukemia", "Undifferentiated Acute Leukemia", "Acute undifferentiated leukemia", "leukemia acute undifferentiated", "acute undifferentiated leukemia", "undifferentiated acute leukemia", "Acute Undifferentiated Leukemia", "Acute undifferentiated leukaemia", "Undifferentiated type acute leukemia", "Undifferentiated type acute leukaemia", "Acute Leukemia Not Otherwise Specified", "acute undifferentiated leukemia (diagnosis)", "Acute myeloblastic leukemia - undifferentiated", "Acute myeloblastic leukaemia - undifferentiated", "M0 - Acute myeloblastic leukemia - undifferentiated", "M0 - Acute myeloblastic leukaemia - undifferentiated", "Acute myeloid leukemia, minimal differentiation, FAB M0", "acute myeloid leukemia, minimal differentiation, FAB M0", "Acute myeloid leukaemia, minimal differentiation, FAB M0", "acute myelogenous leukemia, minimal differentiation, FAB M0", "Acute myeloid leukemia, minimal differentiation, FAB M0 (disorder)", "acute myelogenous leukemia, minimal differentiation, FAB M0 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute undifferentiated leukemia", "shortest_name_length": 3}
{"curie": "MONDO:0003185", "names": ["Adenocystic Breast Carcinoma", "adenoid cystic breast cancer", "adenocystic breast carcinoma", "Mammary Adenocystic carcinoma", "mammary adenocystic carcinoma", "Mammary Adenocystic Carcinoma", "Adenoid Cystic Breast Carcinoma", "breast adenoid cystic carcinoma", "Adenoid cystic breast carcinoma", "adenoid cystic breast carcinoma", "Adenocystic Carcinoma of Breast", "adenocystic carcinoma of breast", "Breast Adenoid Cystic Carcinoma", "mammary adenoid cystic carcinoma", "Adenoid Cystic Carcinoma of Breast", "adenoid cystic carcinoma of breast", "Adenocystic Carcinoma of the Breast", "adenocystic carcinoma of the breast", "adenoid cystic carcinoma of the breast", "Adenoid Cystic Carcinoma of the Breast", "adenoid cystic carcinoma of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenoid cystic breast carcinoma", "shortest_name_length": 28}
{"curie": "UMLS:C0948966", "names": ["Malignant nipple neoplasm female", "Female Malignant Nipple Neoplasm", "malignant neoplasm of female nipple", "breast neoplasm malignant female nipple", "Malignant neoplasm of nipple of female breast", "malignant neoplasm of female nipple (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant neoplasm of nipple of female breast", "shortest_name_length": 32}
{"curie": "UMLS:C3501946", "names": ["Microcephaly with Chorioretinopathy, Autosomal Dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Microcephaly with Chorioretinopathy, Autosomal Dominant", "shortest_name_length": 55}
{"curie": "MONDO:0003923", "names": ["Ethmoid Sinus Papilloma", "ethmoid sinus Schneiderian papilloma", "Ethmoid Sinus Schneiderian Papilloma", "Schneiderian Papilloma of Ethmoid Sinus", "Schneiderian papilloma of ethmoid sinus", "Schneiderian papilloma of the ethmoid sinus", "Schneiderian Papilloma of the Ethmoid Sinus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ethmoid sinus Schneiderian papilloma", "shortest_name_length": 23}
{"curie": "MONDO:0004524", "names": ["WDT-UMP", "Atypical Follicular Adenoma", "atypical follicular adenoma", "Atypical follicular adenoma", "thyroid gland atypical follicular adenoma", "Thyroid Gland Atypical Follicular Adenoma", "Atypical follicular adenoma (morphologic abnormality)", "atypical follicular adenoma (morphologic abnormality)", "Thyroid Gland Well-Differentiated Tumor of Uncertain Malignant Potential", "Thyroid Gland Well-Differentiated Neoplasm of Uncertain Malignant Potential"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid gland atypical follicular adenoma", "shortest_name_length": 7}
{"curie": "MONDO:0001890", "names": ["pulp erosion", "Erosion, extending into pulp", "dental pulp tooth erosion, non-bacterial", "tooth erosion, non-bacterial of dental pulp"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulp erosion", "shortest_name_length": 12}
{"curie": "UMLS:C4521826", "names": ["IIA", "Stage IIA Distal Bile Duct Cancer AJCC v8", "Stage IIA Distal Bile Duct Carcinoma AJCC v8", "Stage IIA Extrahepatic (Distal) Bile Duct Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Distal Bile Duct Cancer AJCC v8", "shortest_name_length": 3}
{"curie": "MONDO:0010800", "names": ["DIDMOAD, mitochondrial form", "DIDMOAD SYNDROME, MITOCHONDRIAL FORM", "Wolfram syndrome, mitochondrial form", "Wolfram Syndrome, Mitochondrial Form", "DIDMOAD Syndrome, Mitochondrial Form", "WOLFRAM SYNDROME, MITOCHONDRIAL FORM", "Didmoad syndrome, mitochondrial form", "diabetes mellitus AND insipidus with optic atrophy AND deafness mitochondrial form", "diabetes insipidus and mellitus with optic atrophy and deafness, mitochondrial form", "Diabetes Insipidus And Mellitus With Optic Atrophy And Deafness, Mitochondrial Form", "DIABETES INSIPIDUS AND MELLITUS WITH OPTIC ATROPHY AND DEAFNESS, MITOCHONDRIAL FORM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wolfram syndrome, mitochondrial form", "shortest_name_length": 27}
{"curie": "UMLS:C0862719", "names": ["Carcinoma larynx stage IV", "Larynx carcinoma stage IV", "Stage IV Larynx Carcinoma", "Metastatic Larynx Carcinoma", "Stage IV Carcinoma of Larynx", "Stage IV Laryngeal Carcinoma", "Carcinoma of larynx stage IV", "Metastatic Laryngeal Carcinoma", "Metastatic Carcinoma of Larynx", "Stage IV Carcinoma of the Larynx", "Metastatic Carcinoma of the Larynx"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Laryngeal Carcinoma", "shortest_name_length": 25}
{"curie": "UMLS:C0442893", "names": ["systemic disease", "Systemic disease", "Systemic illness", "disease systemic", "Systemic Disease", "systemic illness", "diseases systemic", "Systemic diseases", "Systemic Disorder", "illnesses systemic", "Systemic disease, NOS", "Systemic disease (disorder)", "Systemic illness (qualifier value)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Systemic disease", "shortest_name_length": 16}
{"curie": "MONDO:0022598", "names": ["brachydactyly absence of distal phalanges"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly absence of distal phalanges", "shortest_name_length": 41}
{"curie": "UMLS:C4521648", "names": ["IA", "Stage IA Esophageal Adenocarcinoma", "Pathologic Stage IA Esophageal Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IA Esophageal Adenocarcinoma AJCC v8", "shortest_name_length": 2}
{"curie": "UMLS:C3273134", "names": ["Extrahepatic Bile Duct Cystadenocarcinoma", "Extrahepatic Bile Duct MCN with an Associated Invasive Carcinoma", "Extrahepatic Bile Duct Mucinous Cystic Neoplasm with an Associated Invasive Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extrahepatic Bile Duct Mucinous Cystic Neoplasm with an Associated Invasive Carcinoma", "shortest_name_length": 41}
{"curie": "UMLS:C2188139", "names": ["Ovarian Undifferentiated Sarcoma", "Undifferentiated Ovarian Sarcoma", "undifferentiated sarcoma of ovary", "undifferentiated sarcoma of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "undifferentiated sarcoma of ovary", "shortest_name_length": 32}
{"curie": "MONDO:0011353", "names": ["atrial septal defect, secundum, with various cardiac and Noncardiac defects", "ATRIAL SEPTAL DEFECT, SECUNDUM, WITH VARIOUS CARDIAC AND NONCARDIAC DEFECTS", "Atrial Septal Defect, Secundum, with Various Cardiac and Noncardiac Defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial septal defect, secundum, with various cardiac and Noncardiac defects", "shortest_name_length": 75}
{"curie": "UMLS:C0267994", "names": ["FLUID ELECTROLYTE DISORDER", "electrolyte fluid disorder", "fluid electrolyte disorders", "Fluid and electrolyte disorders", "FLUID AND ELECTROLYTE DISORDERS", "fluid and electrolyte disorders", "disorder of fluid and/or electrolyte", "Disorder of fluid AND/OR electrolyte", "Disorder of fluid or electrolyte, NOS", "fluid and electrolyte disorders (diagnosis)", "Disorder of fluid AND/OR electrolyte (disorder)", "disorder of fluid or electrolyte or acid-base balance", "DISORDERS OF FLUID, ELECTROLYTE AND ACID-BASE BALANCE", "Disorders of fluid, electrolyte and acid-base balance", "Disorders of fluid, electrolyte, and acid-base balance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disorder of fluid AND/OR electrolyte", "shortest_name_length": 26}
{"curie": "UMLS:C2931888", "names": ["Acrocephalosyndactyly, type 5", "Pfeiffer type acrocephalosyndactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pfeiffer type acrocephalosyndactyly", "shortest_name_length": 29}
{"curie": "MONDO:0008369", "names": ["pRTA", "Type 2 RTA", "type II RTA", "proximal RTA", "proximal rta", "RTA, RATE TYPE", "RTA, rate type", "Proximal Type RTA", "Proximal Type RTAs", "RTA, PROXIMAL TYPE", "RTA, proximal type", "RTA, Proximal Type", "RTAs, Proximal Type", "renal tubular acidosis 2", "RENAL TUBULAR ACIDOSIS II", "Proximal tubular acidosis", "Renal Tubular Acidosis II", "Bicarbonate deficit syndrome", "type 2 renal tubular acidosis", "Type 2 renal tubular acidosis", "renal tubular acidosis type 2", "Renal tubular acidosis type 2", "Renal tubular acidosis, type 2", "Type II Renal Tubular Acidosis", "Type II renal tubular acidosis", "proximal renal tubular acidosis", "Proximal renal tubular acidosis", "Renal tubular acidosis, type II", "acidosis proximal renal tubular", "Proximal Renal Tubular Acidosis", "Bicarbonate reabsorption defect", "Renal Tubular Acidosis, Type II", "Renal tubular acidosis, proximal", "renal tubular acidosis, proximal", "Renal Tubular Acidosis, Proximal", "RENAL TUBULAR ACIDOSIS, PROXIMAL", "Acidosis, Renal Tubular, Type II", "Renal tubular acidosis, rate type", "type II proximal renal tubular acidosis", "proximal (type II) renal tubular acidosis", "Proximal renal tubular acidosis (disorder)", "Renal tubular acidosis, bicarbonate wastage", "RTA Type II - Type II renal tubular acidosis", "RENAL TUBULAR ACIDOSIS PROXIMAL FANCONI SYNDROME", "RENAL TUBULAR ACIDOSIS PROXIMAL <FANCONI SYNDROME>", "type II proximal renal tubular acidosis (diagnosis)", "Renal Tubular Acidosis, Proximal, with Ocular Abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "proximal renal tubular acidosis", "shortest_name_length": 4}
{"curie": "UMLS:C0035956", "names": ["Spontaneous Rupture", "rupture spontaneous", "spontaneous rupture", "Spontaneous Ruptures", "Rupture, Spontaneous", "Ruptures, Spontaneous"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rupture, Spontaneous", "shortest_name_length": 19}
{"curie": "MONDO:0032590", "names": ["ODG8", "ovarian dysgenesis 8", "OVARIAN DYSGENESIS 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian dysgenesis 8", "shortest_name_length": 4}
{"curie": "MONDO:0008161", "names": ["Globodontia", "globodontia", "Otodental Syndrome", "otodental syndrome", "OTODENTAL SYNDROME", "Otodental syndrome", "Otodental Dysplasia", "Otodental dysplasia", "otodental dysplasia", "OTODENTAL DYSPLASIA", "Globodontia (disorder)", "oculootodental syndrome", "Otodental syndrome (disorder)", "otodental syndrome with coloboma", "CHROMOSOME 11q13 DELETION SYNDROME", "Chromosome 11q13 Deletion Syndrome", "chromosome 11q13 deletion syndrome", "otodental dysplasia chromosome deletion syndrome", "Large, bulbous crowns of primary and secondary canines and molars (globodontia)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "otodental syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0018602", "names": ["NSTI", "necrotizing soft tissue infection", "Necrotising soft tissue infection", "Necrotizing soft tissue infection", "Necrotizing soft tissue infection (disorder)", "necrotizing soft tissue infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "necrotizing soft tissue infection", "shortest_name_length": 4}
{"curie": "MONDO:0006086", "names": ["Myxoma", "MYXOMA", "myxoma", "Myxomas", "myxomas", "Myxoma NOS", "Myxoma, NOS", "Angiomyxoma", "angiomyxoma", "Angiomyxomas", "Deep Angiomyxoma", "Myxoma (disorder)", "Aggressive angiomyxoma", "Angiomyxoma (disorder)", "Aggressive Angiomyxoma", "Angiomyxoma (diagnosis)", "Deep \"Aggressive\" Angiomyxoma", "Deep (Aggressive) Angiomyxoma", "Myxoma (morphologic abnormality)", "Aggressive angiomyxoma (disorder)", "Aggressive angiomyxoma (diagnosis)", "Angiomyxoma (morphologic abnormality)", "neoplasm of uncertain behavior angiomyxoma", "neoplasm of uncertain behavior angiomyxoma aggressive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angiomyxoma", "shortest_name_length": 6}
{"curie": "UMLS:C1699329", "names": ["Tracheal Mucositis", "Tracheal mucositis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tracheal Mucositis", "shortest_name_length": 18}
{"curie": "MONDO:0004843", "names": ["Nystagmus", "NYSTAGMUS", "nystagmus", "Nystagmus NOS", "Nystagmus, NOS", "Pathologic Nystagmus", "Nystagmus (disorder)", "pathologic nystagmus", "Unspecified nystagmus", "nystagmus (diagnosis)", "Nystagmus, Pathologic", "Nystagmus, unspecified", "nystagmus (physical finding)", "Involuntary, rapid, rhythmic eye movements"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pathologic nystagmus", "shortest_name_length": 9}
{"curie": "MONDO:0004963", "names": ["T-ALL", "T-cell ALL", "acute T-cell leukemia", "Acute T Cell Leukemia", "Acute T-Cell Leukemia", "acute T cell leukemia", "T-Cell Type Acute Leukemia", "T-cell type acute leukemia", "T Acute Lymphoblastic Leukemia", "T acute lymphoblastic leukemia", "T-Acute Lymphoblastic Leukemia", "acute T-cell lymphocytic leukemia", "Acute T-Cell Lymphocytic Leukemia", "Acute T Cell Lymphocytic Leukemia", "T-cell acute lymphocytic leukemia", "acute T cell lymphocytic leukemia", "Precursor T-Lymphoblastic Leukemia", "precursor T-lymphoblastic leukemia", "T-Cell Acute Lymphoblastic Leukemia", "T-cell acute lymphoblastic leukemia", "acute T-cell lymphoblastic leukemia", "Acute T-Cell Lymphoblastic Leukemia", "Acute T Cell Lymphoblastic Leukemia", "acute T cell lymphoblastic leukemia", "Precursor T-lymphoblastic leukemia (T-cell ALL)", "precursor T-lymphoblastic leukemia (T-cell ALL)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-cell acute lymphoblastic leukemia", "shortest_name_length": 5}
{"curie": "MONDO:0001273", "names": ["Megacolon", "megacolon", "megarectum", "Megarectum", "MEGACOLON AQUIRED", "MEGACOLON ACQUIRED", "Acquired megacolon", "Megacolon acquired", "acquired megacolon", "Dilatation of colon", "dilatation of colon", "Megacolon, not Hirschsprung", "Megacolon, not Hirschsprung's", "acquired megacolon (diagnosis)", "MEGACOLON, ACQUIRED, FUNCTIONAL", "Megacolon, other than Hirschsprung's", "Megacolon, not Hirschsprung's (disorder)", "Megacolon excluding Hirschsprung's disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "megacolon", "shortest_name_length": 9}
{"curie": "UMLS:C1136135", "names": ["Water Stress", "Stress, Water"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Water Stress", "shortest_name_length": 12}
{"curie": "MONDO:0003534", "names": ["Thymus papillary carcinoma", "Thymus Papillary Carcinoma", "thymic papillary carcinoma", "Thymic Papillary Carcinoma", "Papillary Carcinoma of Thymus", "papillary carcinoma of Thymus", "thymic papillary adenocarcinoma", "papillary thymic adenocarcinoma", "Thymic Papillary Adenocarcinoma", "thymus papillary adenocarcinoma", "Papillary carcinoma of the Thymus", "Papillary Carcinoma of the Thymus", "papillary carcinoma of the Thymus", "Thymic Low-Grade Papillary Adenocarcinoma", "Thymic Low Grade Papillary Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papillary thymic adenocarcinoma", "shortest_name_length": 26}
{"curie": "UMLS:C5447259", "names": ["Recurrent Low Grade Astrocytoma", "Recurrent Low Grade Astrocytic Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Low Grade Astrocytoma", "shortest_name_length": 31}
{"curie": "MONDO:0002691", "names": ["Liver Cancer", "Liver cancer", "liver cancer", "LIVER CANCER", "Liver--Cancer", "Cancer, Liver", "Liver Cancers", "liver cancers", "Hepatic cancer", "Hepatic Cancer", "Cancers, Liver", "hepatic cancer", "Hepatic Cancers", "Cancer of Liver", "cancer of liver", "Cancer, Hepatic", "Liver, cancer of", "Cancers, Hepatic", "hepatic neoplasm", "neoplasm of liver", "CA - Liver cancer", "Ca liver - primary", "ca liver - primary", "cancer of the liver", "Cancer of the Liver", "primary cancer liver", "Primary liver cancer", "primary liver cancer", "Neoplasm malig;liver", "liver tumor or cancer", "Malignant liver tumor", "Hepatocellular Cancer", "liver malignant tumors", "Hepatocellular Cancers", "Malignant liver tumour", "CANCER, HEPATOCELLULAR", "Cancer, Hepatocellular", "Cancers, Hepatocellular", "Primary cancer of liver", "primary cancer of liver", "Hepatic tumor malignant", "of primary liver cancer", "Cancer of liver, primary", "malignant liver neoplasm", "Hepatic tumour malignant", "Malignant tumor of liver", "malignant tumor of liver", "liver cancer (diagnosis)", "liver neoplasm malignant", "Malignant tumour of liver", "Liver, cancer of, primary", "Cancer of liver resectable", "Malignant hepatic neoplasm", "primary tumor of the liver", "HEPATIC NEOPLASM MALIGNANT", "Hepatic neoplasm malignant", "Hepatic neoplasms malignant", "malignant neoplasm of liver", "Malignant neoplasm of liver", "Liver, cancer of, resectable", "Hepatic neoplasm malignant NOS", "liver neoplasm malignant primary", "Malignant liver tumor resectable", "primary malignant liver neoplasm", "liver malignant neoplasm primary", "Primary Malignant Liver Neoplasm", "malignant neosplasm of the liver", "Malignant neoplasm of liver, NOS", "Malignant liver tumour resectable", "malignant hepato-biliary neoplasm", "Resectable Malignant Liver Neoplasm", "primary malignant neoplasm of liver", "Primary malignant neoplasm of liver", "Primary Malignant Neoplasm of Liver", "Malignant neoplasm of liver, primary", "malignant neoplasm of liver, primary", "Malignant hepatic neoplasm resectable", "Hepatic neoplasm malignant resectable", "Resectable Hepatic Malignant Neoplasm", "Resectable Malignant Neoplasm of Liver", "Malignant neoplasm of liver (disorder)", "Resectable malignant neoplasm of Liver", "Resectable malignant neoplasm of liver", "malignant neoplasm of liver (diagnosis)", "Malignant neoplasm of liver, unspecified", "resectable malignant neoplasm of the liver", "Primary malignant neoplasm of liver (disorder)", "primary malignant neoplasm of liver (diagnosis)", "non-resectable primary hepatic malignant neoplasm", "Malignant neoplasm of liver, not specified as primary or secondary", "malignant neoplasm of liver, not specified as primary or secondary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "liver cancer", "shortest_name_length": 12}
{"curie": "MONDO:0007490", "names": ["carpotarsal osteochondromatosis", "Carpotarsal osteochondromatosis", "Maroteaux-Le Merrer-Bensahel syndrome", "Maroteaux Le-Merrer Bensahel syndrome", "Maroteaux Le Merrer Bensahel syndrome", "dominant carpotarsal osteochondromatosis", "Osteochondromatosis, Dominant Carpotarsal", "osteochondromatosis, dominant carpotarsal", "OSTEOCHONDROMATOSIS, DOMINANT CARPOTARSAL", "Carpotarsal osteochondromatosis (disorder)", "Dysplasia Epiphysealis Hemimelica with Chondromas and Osteochondromas", "dysplasia epiphysealis hemimelica with CHONDROMAS and osteochondromas", "DYSPLASIA EPIPHYSEALIS HEMIMELICA WITH CHONDROMAS AND OSTEOCHONDROMAS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carpotarsal osteochondromatosis", "shortest_name_length": 31}
{"curie": "MONDO:0018149", "names": ["Hurler variant", "Caffey syndrome", "Landing disease", "GLB1 Deficiency", "pseudo-Hurler's", "GLB1 DEFICIENCY", "GLB1 deficiency", "caffey syndrome", "Landing syndrome", "GLB 1 deficiency", "Deficiency, GLB1", "Gangliosidosis GM1", "Deficiencies, GLB1", "gangliosidosis GM1", "GM1 Gangliosidosis", "gangliosidosis gm1", "GM1 gangliosidosis", "gm1 gangliosidosis", "gangliosidosis; GM1", "Beta-Galactosidosis", "Beta Galactosidosis", "Gangliosidosis, GM1", "GM1; gangliosidosis", "Beta-galactosidosis", "GM>1< gangliosidosis", "G(M1) Gangliosidosis", "Gangliosidosis G(M1)", "Hurler-like syndrome", "pseudo-Hurler disease", "Norman-Landing syndrome", "neurovisceral lipidosis", "GM1 gangliosidosis, NOS", "gagliosidosis GM1, type I", "cerebral GM1 gangliosidosis", "pseudo-Hurler's (diagnosis)", "beta-Galactosidase deficiency", "beta-galactosidase deficiency", "GM1 gangliosidosis (disorder)", "beta-Galactosidase Deficiency", "beta Galactosidase Deficiency", "neuronal Gm(1) gangliosidosis", "beta galactosidase deficiency", "Beta-galactosidase deficiency", "Caffey pseudo-Hurler syndrome", "GM1 gangliosidosis (diagnosis)", "Deficiency, beta Galactosidase", "Deficiency, beta-Galactosidase", "Beta-galactosidase-1 deficiency", "Beta galactosidase 1 deficiency", "beta Galactosidase 1 Deficiency", "beta-Galactosidase-1 Deficiency", "BETA-GALACTOSIDASE-1 DEFICIENCY", "beta-galactosidase-1 deficiency", "deficiency of beta-galactosidase", "Deficiency of beta-galactosidase", "familial neurovisceral lipidosis", "Deficiency, beta-Galactosidase-1", "generalized infantile gangliosidosis", "Decreased beta-galactosidase activity", "Decreased beta galactosidase activity", "beta-galactosidase-1 (GLB1) deficiency", "generalized gangliosidosis GM1, type I", "Beta-Galactosidase-1 (GLB1) Deficiency", "Beta-Galactosidase-1 Deficiency Disease", "beta-Galactosidase isoenzyme deficiency", "Beta Galactosidase 1 Deficiency Disease", "Deficiency of beta-galactosidase (disorder)", "Tay-Sachs disease with visceral involvement", "generalized infantile gangliosidosis with bony involvement", "Beta-galactosidase deficiency in fibroblasts and white blood cells", "Decreased beta-galactosidase activity (leukocyte, fibroblast, plasma)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "GM1 gangliosidosis", "shortest_name_length": 14}
{"curie": "MONDO:0017781", "names": ["Del(12)(p12.1)", "monosomy 12p12.1", "12p12.1 microdeletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "12p12.1 microdeletion syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0004237", "names": ["RLCLC", "large cell carcinoma with rhabdoid phenotype", "Large cell carcinoma with rhabdoid phenotype", "Large Cell Carcinoma with Rhabdoid Phenotype", "large cell lung carcinoma with rhabdoid phenotype", "Lung Large Cell Carcinoma with Rhabdoid Phenotype", "large cell lung carcinoma with Rhabdoid Phenotype", "Large Cell Lung Carcinoma with Rhabdoid Phenotype", "large cell carcinoma of lung with rhabdoid phenotype", "large cell carcinoma with rhabdoid phenotype (diagnosis)", "large cell carcinoma of lung with rhabdoid phenotype (diagnosis)", "large cell carcinoma with rhabdoid phenotype (morphologic abnormality)", "Large cell carcinoma with rhabdoid phenotype (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "large cell carcinoma with rhabdoid phenotype", "shortest_name_length": 5}
{"curie": "UMLS:C5235895", "names": ["Unresectable Adenoid Cystic Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Adenoid Cystic Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0005503", "names": ["Developmental mental disorder", "developmental mental disorder", "mental; developmental disorder", "developmental disorder; mental", "developmental disorder of mental health", "Developmental mental disorder (disorder)", "developmental mental disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental disorder of mental health", "shortest_name_length": 29}
{"curie": "MONDO:0006747", "names": ["enterotoxemia", "Enterotoxemia", "Enterotoxemias", "Enterotoxaemia", "Enterotoxemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "enterotoxemia", "shortest_name_length": 13}
{"curie": "UMLS:C2982964", "names": ["Stage IV Penile Cancer", "Stage IV Penis Cancer AJCC v6", "Stage IV Penile Cancer AJCC v6", "Penile Cancer Stage IV AJCC v6", "Stage IV Penis Carcinoma AJCC v6", "Stage IV Penile Carcinoma AJCC v6", "Stage IV Carcinoma of Penis AJCC v6", "Stage IV Carcinoma of the Penis AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Penile Cancer AJCC v6", "shortest_name_length": 22}
{"curie": "UMLS:C0019275", "names": ["Hernia without Mention of Obstruction or Gangrene", "Hernia NOS without mention of obstruction or gangrene", "Hernia of unspecified site without mention of obstruction or gangrene", "Hernia of other specified sites without mention of obstruction or gangrene"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hernia of unspecified site without mention of obstruction or gangrene", "shortest_name_length": 49}
{"curie": "MONDO:0019972", "names": ["dural sinus malformation", "cranial dural arteriovenous fistula", "cranial dural arteriovenous malformations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dural sinus malformation", "shortest_name_length": 24}
{"curie": "UMLS:C1167648", "names": ["Abdominal and Gastrointestinal Infection", "Abdominal and gastrointestinal infections"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abdominal and gastrointestinal infections", "shortest_name_length": 40}
{"curie": "UMLS:C1868771", "names": ["Peritoneal cloudy effluent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peritoneal cloudy effluent", "shortest_name_length": 26}
{"curie": "UMLS:C1611725", "names": ["Leukemic infiltration brain", "Leukaemic infiltration brain", "Leukemic Infiltration of Brain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leukaemic infiltration brain", "shortest_name_length": 27}
{"curie": "MONDO:0004132", "names": ["anal canal squamous cell carcinoma", "Anal canal squamous cell carcinoma", "Anal Canal Squamous Cell Carcinoma", "squamous cell carcinoma of anal canal", "squamous cell carcinoma of the anal canal", "squamous cell carcinoma of anal canal (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anal canal squamous cell carcinoma", "shortest_name_length": 34}
{"curie": "UMLS:C0862601", "names": ["Metastatic Vaginal Adenocarcinoma", "Vaginal adenocarcinoma metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal adenocarcinoma metastatic", "shortest_name_length": 33}
{"curie": "UMLS:C5239035", "names": ["Sacral Spine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sacral Spine Neoplasm", "shortest_name_length": 21}
{"curie": "MONDO:0014573", "names": ["CLCRP2", "Cole-Carpenter syndrome 2", "COLE-CARPENTER SYNDROME 2", "COLE-CARPENTER syndrome 2", "SEC24D Cole-Carpenter syndrome", "Cole-Carpenter syndrome type 2", "Cole-Carpenter syndrome caused by mutation in SEC24D"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cole-Carpenter syndrome 2", "shortest_name_length": 6}
{"curie": "MONDO:0006753", "names": ["E. coli meningitis", "Meningitis due to E. coli", "Escherichia coli meningitis", "Escherichia coli Meningitis", "Escherichia coli; meningitis", "Meningitis, Escherichia coli", "meningitis; Escherichia coli", "meningitis (Escherichia coli)", "Escherichia coli Meningitides", "Meningitides, Escherichia coli", "meningitis due to Escherichia coli", "Meningitis due to Escherichia coli", "Escherichia coli meningitis (disorder)", "meningitis due to Escherichia coli (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Escherichia coli meningitis", "shortest_name_length": 18}
{"curie": "MONDO:0008046", "names": ["autosomal dominant myoglobinuria", "Autosomal dominant myoglobinuria", "myoglobinuria, autosomal dominant", "MYOGLOBINURIA, AUTOSOMAL DOMINANT", "Myoglobinuria, Autosomal Dominant", "Autosomal dominant myoglobinuria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant myoglobinuria", "shortest_name_length": 32}
{"curie": "UMLS:C4526710", "names": ["Tumor Stage (Pathological)", "Lung Cancer by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Cancer by AJCC v8 Stage", "shortest_name_length": 26}
{"curie": "MONDO:0010319", "names": ["MRXE", "MRXSH", "X-linked mental retardation with epilepsy", "MENTAL RETARDATION, X-LINKED, WITH EPILEPSY", "Mental Retardation, X-Linked, with Epilepsy", "mental retardation, X-linked, with epilepsy", "X-linked intellectual disability Hedera type", "X-linked intellectual disability, Hedera type", "X-linked intellectual disability with epilepsy", "intellectual disability, X-linked, with epilepsy", "mental retardation, X-linked, syndromic, Hedera type", "MENTAL RETARDATION, X-LINKED, SYNDROMIC, HEDERA TYPE", "syndromic X-linked intellectual disability Hedera type", "X-linked intellectual disability Hedera type (disorder)", "intellectual disability, X-linked, syndromic, Hedera type", "X-linked intellectual disability, Hedera type (diagnosis)", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, HEDERA TYPE", "intellectual developmental disorder, X-linked, syndromic, Hedera type, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic X-linked intellectual disability Hedera type", "shortest_name_length": 4}
{"curie": "MONDO:0012042", "names": ["HSCR8", "Hirschsprung disease, susceptibility to, 8", "HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hirschsprung disease, susceptibility to, 8", "shortest_name_length": 5}
{"curie": "MONDO:0017791", "names": ["high bone mass OI", "high bone mass osteogenesis imperfecta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "high bone mass osteogenesis imperfecta", "shortest_name_length": 17}
{"curie": "MONDO:0020367", "names": ["JOAG", "juvenile glaucoma", "Juvenile glaucoma", "Childhood glaucoma", "Glaucoma, juvenile", "Pediatric glaucoma", "childhood glaucoma", "Infantile glaucoma", "Paediatric glaucoma", "Glaucoma in children", "glaucoma of childhood", "Glaucoma of childhood", "Developmental glaucoma", "juvenile open angle glaucoma", "childhood glaucoma (disease)", "pediatric glaucoma (disease)", "glaucoma (disease) of childhood", "Glaucoma of childhood (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile open angle glaucoma", "shortest_name_length": 4}
{"curie": "MONDO:0012022", "names": ["OFC4", "Orofacial Cleft 4", "OROFACIAL CLEFT 4", "orofacial cleft 4", "nonsyndromic cleft lip with or without cleft palate 4", "CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 4", "Cleft Lip with or without Cleft Palate, Nonsyndromic, 4", "cleft lip with or without cleft palate, nonsyndromic, 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orofacial cleft 4", "shortest_name_length": 4}
{"curie": "UMLS:C0948284", "names": ["Corneal Decompensation", "Corneal decompensation", "Corneal decompensation (disorder)", "Corneal Endothelial Decompensation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Corneal decompensation", "shortest_name_length": 22}
{"curie": "MONDO:0012569", "names": ["MVP3", "MMVP3", "MITRAL VALVE PROLAPSE 3", "mitral valve prolapse 3", "myxomatous mitral valve prolapse 3", "Myxomatous Mitral Valve Prolapse 3", "MYXOMATOUS MITRAL VALVE PROLAPSE 3", "MITRAL VALVE PROLAPSE, MYXOMATOUS 3", "mitral valve prolapse, myxomatous 3", "Mitral Valve Prolapse, Myxomatous 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitral valve prolapse, myxomatous 3", "shortest_name_length": 4}
{"curie": "UMLS:C2983571", "names": ["Vulvar Cancer by AJCC v6 Stage", "Vulvar Carcinoma by AJCC v6 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Cancer by AJCC v6 Stage", "shortest_name_length": 30}
{"curie": "MONDO:0022402", "names": ["type I lissencephaly", "agyria-pachygyria type 1", "Bielchowsky type of lissencephaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "agyria-pachygyria type 1", "shortest_name_length": 20}
{"curie": "UMLS:C4329970", "names": ["Factor X Inactivation", "Factor X Inhibitor Present"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Factor X Inactivation", "shortest_name_length": 21}
{"curie": "UMLS:C1710173", "names": ["Basaloid Squamous Cell Lung Carcinoma", "Lung Basaloid Squamous Cell Carcinoma", "Lung Basaloid Squamous Cell  Carcinoma", "Basaloid squamous cell carcinoma of lung", "Squamous Cell Lung Carcinoma, Basaloid Variant", "lung malignant carcinoma squamous cell basaloid", "Basaloid squamous cell carcinoma of lung (disorder)", "Basaloid squamous cell carcinoma of lung (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Basaloid squamous cell carcinoma of lung", "shortest_name_length": 37}
{"curie": "UMLS:C5447394", "names": ["Tissue or Organ Disruption"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tissue or Organ Disruption", "shortest_name_length": 26}
{"curie": "UMLS:C2861599", "names": ["Relapsed Acute Myelomonocytic Leukemia", "Recurrent Acute Myelomonocytic Leukemia", "acute myelomonocytic leukemia in relapse", "leukemia acute myelomonocytic in relapse", "Acute myelomonocytic leukemia, in relapse", "acute myelomonocytic leukemia in relapse (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myelomonocytic leukemia in relapse", "shortest_name_length": 38}
{"curie": "UMLS:C0036939", "names": ["folie deux", "deux folie", "Folie a deux", "Folie à deux", "folie a deux", "Folie a Deux", "Folie A Deux", "folie à deux", "Folie a Trois", "induced psychosis", "Induced psychosis", "psychosis; induced", "induced; psychosis", "symbiotic psychosis", "delusional; induced", "induced; delusional", "Symbiotic psychosis", "psychosis; symbiotic", "symbiotic; psychosis", "Shared paranoid disorder", "shared paranoid disorder", "Shared Paranoid Disorder", "shared psychotic disorder", "Induced paranoid disorder", "Disorder, Shared Paranoid", "Shared Paranoid Disorders", "Shared psychotic disorder", "Shared Psychotic Disorder", "Paranoid Disorder, Shared", "Induced psychotic disorder", "induced psychotic disorder", "Disorder, Shared Psychotic", "Paranoid Disorders, Shared", "Psychotic Disorder, Shared", "Shared Psychotic Disorders", "Disorders, Shared Paranoid", "induced paranoid disorders", "disorder; paranoid, induced", "paranoid; disorder, induced", "Disorders, Shared Psychotic", "Psychotic Disorders, Shared", "Induced delusional disorder", "psychotic; disorder, induced", "disorder; psychotic, induced", "shared paranoid disorder (diagnosis)", "shared psychotic disorder (diagnosis)", "Induced psychotic disorder (disorder)", "Induced psychosis or paranoid disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Shared Paranoid Disorder", "shortest_name_length": 10}
{"curie": "MONDO:0018709", "names": ["X-linked intellectual disability-hypotonia-movement disorder syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability-hypotonia-movement disorder syndrome", "shortest_name_length": 69}
{"curie": "UMLS:C2986666", "names": ["Stage I Liver Cancer", "Stage I Adult Liver Cancer AJCC v7", "stage I adult primary liver cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Adult Liver Cancer AJCC v7", "shortest_name_length": 20}
{"curie": "UMLS:C0740376", "names": ["cerebral artery thrombosis middle", "Middle Cerebral Artery Thrombosis", "artery cerebral middle thrombosis", "middle cerebral artery thrombosis", "Middle cerebral artery thrombosis", "Thrombosis, Middle Cerebral Artery", "thrombosis; middle cerebral artery", "Thrombosis of middle cerebral artery", "middle cerebral artery thrombosis (diagnosis)", "Thrombosis of middle cerebral artery (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Middle Cerebral Artery Thrombosis", "shortest_name_length": 33}
{"curie": "UMLS:C1333554", "names": ["FIGO Stage IIC GTT", "FIGO Stage IIC Gestational Trophoblastic Tumor", "FIGO Stage IIC Gestational Trophoblastic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Stage IIC Gestational Trophoblastic Tumor", "shortest_name_length": 18}
{"curie": "UMLS:C1278797", "names": ["Postnatal infection", "Postnatal infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postnatal infection", "shortest_name_length": 19}
{"curie": "MONDO:0005384", "names": ["Focal Epilepsy", "Local epilepsy", "Focal epilepsy", "focal epilepsy", "local epilepsy", "epilepsy focal", "Epilepsy, Focal", "Epilepsy, focal", "epilepsy; focal", "focal; epileptic", "Partial Epilepsy", "Partial epilepsy", "partial epilepsy", "Focal Epilepsies", "Epilepsy, Partial", "epilepsy; partial", "Epilepsies, Focal", "Partial Epilepsies", "partial; epileptic", "Focal epilepsy, NOS", "Epilepsies, Partial", "Epilepsy, focal NOS", "Epilepsy, partial NOS", "SEIZURE DISORDER FOCAL", "Focal Seizure Disorder", "focal seizure disorder", "Focal Seizure Disorders", "Seizure Disorder, Focal", "Seizure Disorders, Focal", "Disorders, Focal Seizure", "partial seizure disorder", "Partial Seizure Disorder", "Seizure Disorder, Partial", "Partial Seizure Disorders", "Seizure Disorders, Partial", "Disorders, Partial Seizure", "epilepsy localization-related", "Localization-Related Epilepsy", "Localisation related epilepsy", "localisation-related epilepsy", "Localisation-related epilepsy", "Localization related epilepsy", "Localization-related epilepsy", "Epilepsy, Localization-Related", "epilepsy; localization-related", "LOCALIZATION-RELATED EPILEPSIES", "Localization-Related Epilepsies", "Epilepsies, Localization-Related", "Localization-related epilepsy, NOS", "Localization-related epilepsy (disorder)", "Localization-related epilepsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal epilepsy", "shortest_name_length": 14}
{"curie": "UMLS:C1333865", "names": ["Grade 2 Rectal Adenocarcinoma", "Grade II Rectal Adenocarcinoma", "Moderately Differentiated Rectal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade 2 Rectal Adenocarcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0017835", "names": ["HES-L", "lymphoid HES", "lymphocytic variant HES", "lymphocytic hypereosinophilic syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphocytic hypereosinophilic syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C4727007", "names": ["Metastatic Bone Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Bone Sarcoma", "shortest_name_length": 23}
{"curie": "MONDO:0017659", "names": ["sporadic hyperekplexia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sporadic hyperekplexia", "shortest_name_length": 22}
{"curie": "MONDO:0006398", "names": ["Retroperitoneal Inflammatory Myofibroblastic Tumor", "retroperitoneal inflammatory myofibroblastic tumor", "retroperitoneal space inflammatory myofibroblastic tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retroperitoneal inflammatory myofibroblastic tumor", "shortest_name_length": 50}
{"curie": "MONDO:0002851", "names": ["Mediastinal Rhabdomyosarcoma", "mediastinum rhabdomyosarcoma", "mediastinal rhabdomyosarcoma", "Rhabdomyosarcoma of Mediastinum", "Rhabdomyosarcoma of mediastinum", "rhabdomyosarcoma of mediastinum", "rhabdomyosarcoma of the mediastinum", "Rhabdomyosarcoma of the Mediastinum", "mediastinum rhabdomyosarcoma (disease)", "mediastinal myosarcoma rhabdomyosarcoma", "rhabdomyosarcoma (disease) of mediastinum", "rhabdomyosarcoma of mediastinum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mediastinum rhabdomyosarcoma", "shortest_name_length": 28}
{"curie": "UMLS:C4745280", "names": ["Melanoma of Unknown Primary", "Melanoma of Unknown Primary Origin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Melanoma of Unknown Primary", "shortest_name_length": 27}
{"curie": "UMLS:C5237463", "names": ["Recurrent Mature B-Cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Mature B-Cell Non-Hodgkin Lymphoma", "shortest_name_length": 44}
{"curie": "MONDO:0032738", "names": ["MEGD", "GDRM", "BKGK", "Kennerknecht syndrome", "KENNERKNECHT syndrome", "BROSNAN-KENNERKNECHT-GURAN-KOC SYNDROME", "MYOECTODERMAL GONADAL DYSGENESIS SYNDROME", "gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy", "GONADAL DYSGENESIS, DYSMORPHIC FACIES, RETINAL DYSTROPHY, AND MYOPATHY", "agonadism, 46,XY, with mental retardation, short stature, retarded bone age, and multiple extragenital malformations", "agonadism, 46,XY, with intellectual disability, short stature, retarded bone age, and multiple extragenital malformations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy", "shortest_name_length": 4}
{"curie": "MONDO:0009249", "names": ["HFI", "Fructosemia", "fructosemia", "FRUCTOSEMIA", "Fructosaemia", "Fructosemias", "ALDB deficiency", "Aldob deficiency", "ALDOB DEFICIENCY", "ALDOB Deficiency", "Deficiency, ALDOB", "ALDOB Deficiencies", "Deficiencies, ALDOB", "fructose intolerance", "Fructose Intolerance", "Fructose intolerance", "FRUCTOSE INTOLERANCE", "Aldolase B deficiency", "ALDOLASE B DEFICIENCY", "aldolase B deficiency", "Aldolase B Deficiency", "Intolerance, Fructose", "intolerance; fructose", "Fructose Intolerances", "fructose; intolerance", "Hereditary fructosuria", "hereditary fructosemia", "Hereditary fructosemia", "Intolerances, Fructose", "Deficiency, Aldolase B", "Fructose malabsorption", "Aldolase B Deficiencies", "Deficiencies, Aldolase B", "Fructose intolerance, NOS", "ALDB - aldolase B deficiency", "ALDB - aldolose B deficiency", "Fructose Aldolase B Deficiency", "Hereditary fructose intolerance", "fructose hereditary intolerance", "Fructose intolerance hereditary", "hereditary fructose intolerance", "fructose intolerance hereditary", "Hereditary Fructose Intolerance", "fructose intolerance, hereditary", "Fructose Intolerance, Hereditary", "fructose intolerance (diagnosis)", "FRUCTOSE INTOLERANCE, HEREDITARY", "Hereditary Fructose Intolerances", "Fructose Intolerances, Hereditary", "fructose-1-phosphate aldolase deficiency", "Fructose-1-phosphate aldolase deficiency", "Hereditary fructose intolerance syndrome", "fructose 1 phosphate aldolase deficiency", "FRUCTOSE-1-PHOSPHATE ALDOLASE DEFICIENCY", "Fructose-1-Phosphate Aldolase Deficiency", "hereditary fructose intolerance syndrome", "Fructose 1 Phosphate Aldolase Deficiency", "Deficiency, Fructose-1-Phosphate Aldolase", "Aldolase Deficiency, Fructose-1-Phosphate", "Fructose-biphosphate aldolase B deficiency", "Fructose-1-Phosphate Aldolase Deficiencies", "Aldolase Deficiencies, Fructose-1-Phosphate", "Deficiencies, Fructose-1-Phosphate Aldolase", "Fructose 1,6 Biphosphate Aldolase Deficiency", "Fructose-1,6-Biphosphate Aldolase Deficiency", "Aldolase Deficiency, Fructose-1,6-Biphosphate", "Deficiency, Fructose-1,6-Biphosphate Aldolase", "Fructose-1,6-Biphosphate Aldolase Deficiencies", "Aldolase Deficiencies, Fructose-1,6-Biphosphate", "FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE B DEFICIENCY", "Fructose-1,6-bisphosphate aldolase B deficiency", "fructose-1,6-bisphosphate aldolase B deficiency", "Deficiencies, Fructose-1,6-Biphosphate Aldolase", "Fructose 1,6 Bisphosphate Aldolase B Deficiency", "Fructose-1,6-Bisphosphate Aldolase B Deficiency", "Hereditary fructose-1-phosphate aldolase deficiency", "hereditary fructose-1-phosphate aldolase deficiency", "Fructose-1,6-bisphosphate aldolase B deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary fructose intolerance", "shortest_name_length": 3}
{"curie": "UMLS:C3640962", "names": ["Stage 2B Neuroblastoma", "Stage IIB Neuroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 2B Neuroblastoma", "shortest_name_length": 22}
{"curie": "MONDO:0013207", "names": ["FECD7", "Fcd4 locus", "FCD4 LOCUS", "corneal dystrophy, fuchs endothelial, 7", "CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 7", "Corneal Dystrophy, Fuchs Endothelial, 7", "corneal dystrophy, Fuchs endothelial, 7", "CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, LATE-ONSET", "corneal dystrophy, Fuchs endothelial, late-onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal dystrophy, fuchs endothelial, 7", "shortest_name_length": 5}
{"curie": "MONDO:0001758", "names": ["Accessory Sinus Sarcoma", "Paranasal Sinus Sarcoma", "accessory sinus sarcoma", "paranasal sinus sarcoma", "Sarcoma of Paranasal Sinus", "sarcoma of paranasal sinus", "Sarcoma of Accessory Sinus", "sarcoma of Accessory sinus", "sarcoma of accessory sinus", "sarcoma of the accessory sinus", "Sarcoma of the Paranasal Sinus", "sarcoma of the paranasal sinus", "Sarcoma of the Accessory Sinus", "sarcoma of accessory sinus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paranasal sinus sarcoma", "shortest_name_length": 23}
{"curie": "MONDO:0100368", "names": ["RP20", "LCA2", "retinitis pigmentosa 20", "RPE65 retinitis pigmentosa", "recessive RPE65 retinopathy", "Leber congenital amaurosis 2", "amaurosis congenita of Leber 2", "amaurosis congenita of Leber II", "RPE65 Leber congenital amaurosis", "Leber congenital amaurosis type 2", "RPE65-related recessive retinopathy", "amaurosis congenita of Leber, type 2", "retinitis pigmentosa caused by mutation in RPE65", "Leber congenital amaurosis caused by mutation in RPE65"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "RPE65-related recessive retinopathy", "shortest_name_length": 4}
{"curie": "UMLS:C1707828", "names": ["Ductal Eccrine Carcinoma with Spindle Cell Elements"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ductal Eccrine Carcinoma with Spindle Cell Elements", "shortest_name_length": 51}
{"curie": "MONDO:0011942", "names": ["SLEN1", "systemic lupus erythematosus with nephritis, susceptibility to, 1", "SYSTEMIC LUPUS ERYTHEMATOSUS WITH NEPHRITIS, SUSCEPTIBILITY TO, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "systemic lupus erythematosus with nephritis, susceptibility to, 1", "shortest_name_length": 5}
{"curie": "MONDO:0014648", "names": ["ARS", "AL-RAQAD SYNDROME", "Al-Raqad syndrome", "AL-RAQAD syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Al-Raqad syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C0019340", "names": ["herpes", "Herpes", "HERPES", "Herpes NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Herpes NOS", "shortest_name_length": 6}
{"curie": "MONDO:0012670", "names": ["DFNB63", "autosomal recessive deafness 63", "Deafness, Autosomal Recessive 63", "DEAFNESS, AUTOSOMAL RECESSIVE 63", "deafness, autosomal recessive 63", "deafness, autosomal recessive type 63", "autosomal recessive nonsyndromic deafness 63", "LRTOMT autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 63", "autosomal recessive nonsyndromic deafness type 63", "autosomal recessive nonsyndromic deafness caused by mutation in LRTOMT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 63", "shortest_name_length": 6}
{"curie": "UMLS:C0152452", "names": ["pericardial fibrosis", "Pericardial fibrosis", "Adherent pericardium", "Adhesive pericarditis", "Pericarditis adhesive", "adherent; pericardium", "adhesive pericarditis", "Adherent pericarditis", "pericardium; adherent", "Pericarditis, adhesive", "adhesive; pericarditis", "adherent; pericarditis", "Fibrosis of pericardium", "Adhesive pericarditis (disorder)", "Fibrosis of pericardium (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fibrosis of pericardium", "shortest_name_length": 20}
{"curie": "MONDO:0003387", "names": ["Urethra Clear Cell Adenocarcinoma", "urethra clear cell adenocarcinoma", "urethral clear cell adenocarcinoma", "Urethral Clear Cell Adenocarcinoma", "clear cell adenocarcinoma of urethra", "Clear Cell Adenocarcinoma of Urethra", "Clear cell adenocarcinoma of the urethra", "Clear Cell Adenocarcinoma of the Urethra", "clear cell adenocarcinoma of the urethra", "clear cell adenocarcinoma of urethra (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urethra clear cell adenocarcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0012467", "names": ["CISS2", "cold-induced sweating syndrome 2", "Cold-induced sweating syndrome 2", "COLD-INDUCED SWEATING SYNDROME 2", "CLCF1 cold-induced sweating syndrome", "cold-induced sweating syndrome type 2", "CRISPONI/cold-induced sweating syndrome 2", "Crisponi/Cold-Induced Sweating Syndrome-2", "Crisponi/cold-induced sweating syndrome 2", "CRISPONI/COLD-INDUCED SWEATING SYNDROME 2", "[OBSOLETE] Cold-Induced Sweating Syndrome 1", "cold-induced sweating syndrome caused by mutation in CLCF1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cold-induced sweating syndrome 2", "shortest_name_length": 5}
{"curie": "MONDO:0004254", "names": ["focal intraductal papillomatosis", "Focal Intraductal Papillomatosis", "Localized Intraductal Papillomatosis", "localized intraductal papillomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal intraductal papillomatosis", "shortest_name_length": 32}
{"curie": "UMLS:C1336483", "names": ["stage I soft tissue sarcoma", "Stage I Soft Tissue Sarcoma", "Stage I Sarcoma of Soft Tissue", "Stage I Sarcoma of the Soft Tissue", "Stage I Soft Tissue Sarcoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Soft Tissue Sarcoma AJCC v7", "shortest_name_length": 27}
{"curie": "MONDO:0021629", "names": ["Uterine Ligament Tumor", "uterine ligament tumor", "uterine ligament neoplasm", "Uterine Ligament Neoplasm", "tumor of uterine ligament", "neoplasm of uterine ligament", "Tumor of the Uterine Ligament", "tumor of the uterine ligament", "Neoplasm of the Uterine Ligament", "neoplasm of the uterine ligament", "uterine ligament neoplasm (disease)", "uterine ligament neoplasm (diagnosis)", "neoplasm of uterine ligament (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine ligament neoplasm", "shortest_name_length": 22}
{"curie": "UMLS:C1281915", "names": ["Choroidal infarct", "Choroidal infarction", "Choroidal infarct (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Choroidal infarct", "shortest_name_length": 17}
{"curie": "MONDO:0014734", "names": ["EIG14", "idiopathic generalized epilepsy 14", "susceptibility to idiopathic generalized epilepsy 14", "EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 14", "epilepsy, idiopathic generalized, susceptibility to, 14", "epilepsy, idiopathic generalized, susceptibility to, type 14", "epilepsy, idiopathic generalized, susceptibility to, 14; EIG14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, idiopathic generalized, susceptibility to, 14", "shortest_name_length": 5}
{"curie": "UMLS:C0948862", "names": ["pigment epithelium; retinal detachment", "detachment; retina, pigment epithelium", "Detachment of retinal pigment epithelium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Detachment of retinal pigment epithelium", "shortest_name_length": 38}
{"curie": "MONDO:0008701", "names": ["ACG1A", "Achondrogenesis type 1A", "achondrogenesis type IA", "achondrogenesis type 1A", "ACHONDROGENESIS, TYPE IA", "Achondrogenesis, type IA", "achondrogenesis, type IA", "achondrogenesis, type 1A", "Achondrogenesis, Type Ia", "Houston-Harris achondrogenesis", "Achondrogenesis, type IA (disorder)", "achondrogenesis Houston-Harris type", "achondrogenesis, Houston-Harris type", "ACHONDROGENESIS, HOUSTON-HARRIS TYPE", "Achondrogenesis, Houston-Harris type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "achondrogenesis type IA", "shortest_name_length": 5}
{"curie": "MONDO:0010615", "names": ["IGHD3", "IGHD 3", "IGHD III", "X-linked IGHD", "FLEISHER SYNDROME", "Fleisher syndrome", "fleisher syndrome", "congenital IGHD type III", "Congenital IGHD type III", "isolated growth hormone deficiency type 3", "isolated growth hormone deficiency, type 3", "Congenital isolated GH deficiency type III", "congenital isolated GH deficiency type III", "Isolated growth hormone deficiency, type 3", "X-linked isolated growth hormone deficiency", "isolated growth hormone deficiency type III", "Isolated growth hormone deficiency type III", "isolated growth hormone deficiency, type III", "Isolated Growth Hormone Deficiency, Type III", "Growth hormone deficiency with hypogammaglobulinemia", "Growth Hormone Deficiency with Hypogammaglobulinemia", "growth hormone deficiency with hypogammaglobulinemia", "congenital isolated growth hormone deficiency type III", "Congenital isolated growth hormone deficiency type III", "X-linked agammaglobulinemia with growth hormone deficiency", "X-linked agammaglobulinaemia with growth hormone deficiency", "GROWTH HORMONE DEFICIENCY WITH HYPOGAMMAGLOBULINEMIA, X-LINKED", "X-linked agammaglobulinemia and isolated growth hormone deficiency", "Agammaglobulinemia and isolated growth hormone deficiency, X-linked", "agammaglobulinemia and isolated Growth hormone deficiency, X-linked", "AGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED", "X-linked hypogammaglobulinemia and isolated growth hormone deficiency", "X-linked agammaglobulinemia with growth hormone deficiency (disorder)", "ISOLATED GROWTH HORMONE DEFICIENCY, TYPE III, WITH AGAMMAGLOBULINEMIA", "hypogammaglobulinemia and isolated Growth hormone deficiency, X-linked", "HYPOGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED", "X-linked agammaglobulinemia with growth hormone deficiency (diagnosis)", "Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked", "Nanism due to growth hormone isolated deficiency with X-linked hypogammaglobulinemia", "isolated growth hormone deficiency, type IIi, with agammaglobulinemia, X-linked recessive", "Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia", "Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated growth hormone deficiency type III", "shortest_name_length": 5}
{"curie": "MONDO:0030134", "names": ["OPDM2", "oculopharyngodistal myopathy 2", "OCULOPHARYNGODISTAL MYOPATHY 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculopharyngodistal myopathy 2", "shortest_name_length": 5}
{"curie": "UMLS:C1275212", "names": ["Porocarcinoma in situ", "Porocarcinoma In Situ", "Hidroacanthoma Simplex", "Hidroacanthoma simplex", "Hidroacanthoma simplex of skin", "Hidroacanthoma simplex of skin (disorder)", "Porocarcinoma in situ (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hidroacanthoma simplex", "shortest_name_length": 21}
{"curie": "MONDO:0019024", "names": ["MCS", "MCSL", "Mast Cell Sarcoma", "Mast cell sarcoma", "mast-cell sarcoma", "Mast-Cell Sarcoma", "mast cell sarcoma", "Sarcoma, Mast-Cell", "Sarcoma, Mast Cell", "mast cell; sarcoma", "sarcoma; mast cell", "Mast-Cell Sarcomas", "Sarcomas, Mast-Cell", "sarcoma of mast cell", "Malignant mastocytoma", "Malignant Mastocytoma", "malignant mastocytoma", "mastocytoma; malignant", "malignant; mastocytoma", "Malignant Mastocytomas", "Mastocytoma, Malignant", "Mastocytomas, Malignant", "malignant mast cell tumor", "Malignant mast cell tumor", "Malignant mast cell tumour", "Malignant mast cell tumors", "mast cell; tumor, malignant", "tumor; mast cell, malignant", "Malignant mast cell neoplasm", "mast cell sarcoma (diagnosis)", "malignant mastocytoma (diagnosis)", "Malignant mast cell tumor (disorder)", "Malignant mast cell tumor (clinical)", "malignant mast cell tumor (diagnosis)", "Malignant mast cell tumour (clinical)", "Mast cell sarcoma (morphologic abnormality)", "Malignant mast cell neoplasm (morphologic abnormality)", "malignant neoplasm lymphatic/hematopoietic neoplasm mast cell tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mast cell sarcoma", "shortest_name_length": 3}
{"curie": "MONDO:0017198", "names": ["Ivory bones", "IVORY BONES", "Marble bone", "marble bone", "marble bones", "thicken bone", "MARBLE BONES", "marble; bones", "osteopetrosis", "bones; marble", "osteopetroses", "Osteopetrosis", "Osteopetroses", "OSTEOPETROSIS", "Bone thickened", "BONE THICKENING", "bone thickening", "bones thickening", "bone; thickening", "Albers-Schönberg", "thickening; bone", "Osteopetrosis, NOS", "Marble Bone Disease", "marble bone disease", "Marble bone disease", "bones disease marble", "Disease, Marble Bone", "osteosclerosis fragilis", "Osteosclerosis Fragilis", "osteopetrosis (disease)", "Albers Schönberg Disease", "Albers-Schonberg disease", "congenital osteopetrosis", "Albers-Schonberg Disease", "Albers-Schönberg Disease", "Albers-Schönberg disease", "Osteopetrosis (disorder)", "Congenital osteopetrosis", "Albers Schonberg Disease", "Disease, Albers-Schonberg", "Albers Schoenberg Disease", "osteopetrosis (diagnosis)", "Albers-Schönberg syndrome", "Albers-Schoenberg Disease", "ALBERS-SCHOENBERG DISEASE", "Disease, Albers-Schönberg", "Albers-Schonberg syndrome", "Albers Schoenberg disease", "Albers-Schoenberg disease", "Albers-Schoenberg syndrome", "Albers-Schoonberg syndrome", "Disease, Albers-Schoenberg", "Osteopetrosis generalisata", "Osteopetrosis - congenita type", "osteopetrosis and related disorders", "Harder, denser, fracture-prone bones", "Osteosclerosis Fragilis Generalisata", "Osteosclerosis Fragilis Generalisatas", "OSTEOSCLEROSIS, GENERALIZED CONGENITAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteopetrosis", "shortest_name_length": 11}
{"curie": "MONDO:0015558", "names": ["isolated bone marrow mastocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated bone marrow mastocytosis", "shortest_name_length": 33}
{"curie": "MONDO:0006162", "names": ["colorectal NET G1", "Colorectal NET G1", "colorectum NET G1", "Colorectal Carcinoid Tumor", "colorectal carcinoid tumor", "colorectum carcinoid tumor", "colorectal neuroendocrine tumor G1", "Colorectal Neuroendocrine Tumor G1", "colorectum neuroendocrine neoplasm G1", "large intestinal neuroendocrine tumor G1", "Large Intestinal Neuroendocrine Tumor G1", "grade 1 neuroendocrine neoplasm of colorectum", "colorectum neuroendocrine tumor, well differentiated, low grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorectal neuroendocrine tumor G1", "shortest_name_length": 17}
{"curie": "MONDO:0014546", "names": ["VMCQA", "Vacuolar aggregate myopathy", "myopathy, vacuolar, with CASQ1 aggregates", "MYOPATHY, VACUOLAR, WITH CASQ1 AGGREGATES", "Myopathy due to calsequestrin and SERCA1 protein overload", "myopathy due to calsequestrin and SERCA1 protein overload", "Vacuolar myopathy with sarcoplasmic reticulum protein aggregates", "Myopathy due to calsequestrin and sarcoplasmic/endoplasmic reticulum calcium ATPase 1 protein overload", "Myopathy due to calsequestrin and SERCA1 (sarcoplasmic/endoplasmic reticulum calcium ATPase 1) protein overload", "Myopathy due to calsequestrin and sarcoplasmic/endoplasmic reticulum calcium ATPase 1 protein overload (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy due to calsequestrin and SERCA1 protein overload", "shortest_name_length": 5}
{"curie": "UMLS:C1336409", "names": ["Stage IVC Pharynx Carcinoma", "Pharyngeal Cancer Stage IVC", "Stage IVC Pharyngeal Cancer", "Stage IVC Carcinoma of Pharynx", "Stage IVC Pharyngeal Carcinoma", "Stage IVC Carcinoma of the Pharynx"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Pharyngeal Carcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C1336309", "names": ["Stage II Ovarian Polyembryoma", "Ovarian Polyembryoma Stage II", "Stage II Ovarian Polyembryoma AJCC v6", "Stage II Ovarian Polyembryoma AJCC v7", "Stage II Ovarian Polyembryoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Ovarian Polyembryoma AJCC v6 and v7", "shortest_name_length": 29}
{"curie": "MONDO:0014148", "names": ["ESTRR", "estrogen resistance", "ESTROGEN RESISTANCE", "ESTROGEN INSENSITIVITY", "estrogen insensitivity", "estrogen resistance syndrome", "Estrogen resistance syndrome", "Oestrogen resistance syndrome", "Puberty disorder due to estrogen resistance", "Puberty disorder due to oestrogen resistance", "Puberty disorder due to estrogen resistance (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "estrogen resistance syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C4687639", "names": ["Heart Myxofibrosarcoma", "Cardiac Myxofibrosarcoma", "Heart Myxoid Malignant Fibrous Histiocytoma", "Cardiac Myxoid Malignant Fibrous Histiocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiac Myxofibrosarcoma", "shortest_name_length": 22}
{"curie": "MONDO:0001453", "names": ["Senile reticular degeneration", "Senile reticular retinal degeneration", "senile reticular retinal degeneration", "Senile reticular degeneration of retina", "senile reticular peripheral retinal degeneration", "Senile reticular retinal degeneration (disorder)", "senile reticular retinal degeneration (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "senile reticular retinal degeneration", "shortest_name_length": 29}
{"curie": "MONDO:0000646", "names": ["benign ovary tumor", "benign ovary tumors", "OVARIAN TUMOR BENIGN", "Ovarian tumor benign", "Benign ovarian tumor", "benign ovarian tumor", "Benign Ovarian Tumor", "ovarian tumor benign", "ovarian benign tumor", "Benign tumor of ovary", "benign tumor of ovary", "Ovarian tumour benign", "benign ovarian tumors", "OVARIAN TUMOUR BENIGN", "Benign ovarian tumour", "Benign Tumor of Ovary", "ovary benign neoplasm", "benign ovarian tumour", "Benign tumour of ovary", "ovarian benign neoplasm", "benign ovarian neoplasm", "ovarian neoplasm benign", "Benign Ovarian Neoplasm", "Ovarian neoplasms benign", "benign neoplasm of ovary", "Benign Neoplasm of Ovary", "Benign neoplasm of ovary", "Benign Tumor of the Ovary", "benign tumor of the ovary", "benign neoplasm of the ovary", "Benign Neoplasm of the Ovary", "Benign neoplasm of ovary (disorder)", "benign neoplasm of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian benign neoplasm", "shortest_name_length": 18}
{"curie": "MONDO:0008756", "names": ["Amr syndrome", "AMR syndrome 1", "alopecia-mental retardation syndrome", "Perniola-Krajewska-Carnevale syndrome", "Perniola Krajewska Carnevale syndrome", "Alopecia-intellectual disability syndrome", "alopecia with severe intellectual deficit", "alopecia-intellectual disability syndrome", "alopecia-mental retardation (AMR) syndrome", "alopecia intellectual disbility syndrome 1", "alopecia - intellectual disability syndrome", "alopecia universalis with mental retardation", "alopecia and intellectual disability syndrome", "Alopecia and intellectual disability syndrome", "Neuroectodermosis with alopecia or hypotrichosis", "Alopecia and intellectual disability syndrome (disorder)", "Congenital alopecia, psychomotor retardation, convulsions", "alopecia and intellectual disability syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alopecia - intellectual disability syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0004687", "names": ["Severe NPDR", "severe NPDR", "severe npdr", "Severe nonproliferative retinopathy", "severe nonproliferative retinopathy", "severe nonproliferative diabetic retinopathy", "Severe nonproliferative diabetic retinopathy", "Severe non proliferative diabetic retinopathy", "High risk non proliferative diabetic retinopathy", "high risk non proliferative diabetic retinopathy", "Severe NPDR (nonproliferative diabetic retinopathy)", "diabetes with severe nonproliferative diabetic retinopathy", "Severe nonproliferative retinopathy due to diabetes mellitus", "diabetes with severe nonproliferative diabetic retinopathy (diagnosis)", "Severe nonproliferative retinopathy due to diabetes mellitus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe nonproliferative diabetic retinopathy", "shortest_name_length": 11}
{"curie": "MONDO:0040728", "names": ["infection by vibrio fetus", "Infection by Vibrio fetus", "Infection by Campylobacter fetus", "Infection caused by Vibrio fetus", "infection caused by vibrio fetus", "infection by Campylobacter fetus", "Campylobacter fetus infectious disease", "Infection caused by Campylobacter fetus", "infection caused by Campylobacter fetus", "Infection caused by Campylobacter fetus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Campylobacter fetus infectious disease", "shortest_name_length": 25}
{"curie": "MONDO:0008779", "names": ["AMC", "Guerin-Stern", "Otto Syndrome", "syndrome otto", "Otto syndrome", "Arthrogryposes", "ARTHROGRYPOSIS", "Rossi syndrome", "Rossi Syndrome", "arthrogryposis", "arthrogryposes", "Syndrome, Otto", "Arthrogryposis", "Syndrome, Rossi", "Rossi's syndrome", "amyoplasia congenita", "Myophagism congenita", "Amyoplasia congenita", "Amyoplasia Congenita", "Guerin Stern syndrome", "Guerin-Stern Syndrome", "Guerin-Stern syndrome", "Congenital amyoplasia", "Guérin Stern Syndrome", "Guérin-Stern Syndrome", "Guerin Stern Syndrome", "Syndrome, Guerin-Stern", "Syndrome, Guérin-Stern", "Classic arthrogryposis", "Rocher-Sheldon Syndrome", "Arthrogryposis syndrome", "Rocher-Sheldon syndrome", "Rocher Sheldon Syndrome", "Arthrogryposis multiplex", "Syndrome, Rocher-Sheldon", "neuro-arthromyodysplasia", "Arthrogryposis (disorder)", "arthrogryposis (diagnosis)", "Arthrogryposis, congenital", "Congenital arthromyodysplasia", "Congenital Arthromyodysplasia", "Congenital Arthromyodysplasias", "myodysplasia fibrosa multiplex", "Arthromyodysplasia, Congenital", "multiple congenital contracture", "Arthromyodysplasias, Congenital", "myodysplasia foetalis deformans", "Myodystrophia Fetalis Deformans", "Myodystrophia fetalis deformans", "myodystrophia fetalis deformans", "Multiple congenital contractures", "Myodystrophia foetalis deformans", "multiple congenital contractures", "myodystrophia foetalis deformans", "Congenital contractures, multiple", "arthrogryposis multiplex congenita", "Congenital multiple arthrogryposis", "Congenital Multiple Arthrogryposis", "congenital multiple arthrogryposis", "Multiple congenital arthrogryposis", "Arthrogryposis multiplex congenita", "Arthrogryposis Multiplex Congenita", "Congenital Multiple Arthrogryposes", "congenital multiple Arthrogryposes", "Arthrogryposes, Congenital Multiple", "Arthrogryposis Multiplex Congenitas", "Congenita, Arthrogryposis Multiplex", "multiplex congenita; arthrogryposis", "Arthrogryposes, congenital multiple", "Arthrogryposis, Congenital Multiple", "Multiple Arthrogryposes, Congenital", "Multiplex Congenita, Arthrogryposis", "Multiple Arthrogryposis, Congenital", "arthrogryposis; multiplex congenita", "Congenital multiplex arthrogryposis", "Multiplex Congenitas, Arthrogryposis", "Fibrous Ankylosis of Multiple Joints", "Congenitas, Arthrogryposis Multiplex", "congenital contractures of extremities", "AMC-Arthrogryposis multiplex congenita", "congenital arthromyodysplastic syndrome", "arthrogryposis multiplex congenita (AMC)", "Arthrogryposis Multiplex Congenita (AMC)", "Amyoplasia congenita disruptive sequence", "AMC - Arthrogryposis multiplex congenita", "Arthrogryposis multiplex congenita (AMC)", "Arthrogryposis Multiplex Congenitas (AMC)", "Congenita, Arthrogryposis Multiplex (AMC)", "Multiplex Congenita, Arthrogryposis (AMC)", "Congenitas, Arthrogryposis Multiplex (AMC)", "Multiplex Congenitas, Arthrogryposis (AMC)", "arthrogryposis multiplex congenita (diagnosis)", "Amyoplasia congenita disruptive sequence (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis", "shortest_name_length": 3}
{"curie": "UMLS:C0271125", "names": ["Ciliary Body Implantation Cyst", "Implantation Cyst of Ciliary Body", "Implantation cyst of ciliary body", "Implantation Cyst of the Ciliary Body", "Implantation cyst of ciliary body (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Implantation cyst of ciliary body", "shortest_name_length": 30}
{"curie": "MONDO:0044710", "names": ["Lip/oral cavity squam. cell car.", "lip/oral cavity squam. cell car.", "Lip and Oral Cavity Squamous Cell Cancer", "lip and oral cavity squamous cell cancer", "epidermoid carcinoma, lip and oral cavity", "lip and oral cavity squamous cell carcinoma", "oral cavity and lip squamous cell carcinoma", "Lip and Oral Cavity Squamous Cell Carcinoma", "Lip and oral cavity squamous cell carcinoma", "squamous cell carcinoma, lip and oral cavity", "Squamous cell carcinoma of oral cavity and lip", "squamous cell carcinoma of oral cavity and lip"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lip and oral cavity squamous cell carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0016592", "names": ["non-hereditary degenerative ataxia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-hereditary degenerative ataxia", "shortest_name_length": 34}
{"curie": "MONDO:0001780", "names": ["Prospermia", "ejaculatio praecox", "Ejaculatio praecox", "Ejaculatio Praecox", "Praecox, Ejaculatio", "Ejaculates too soon", "Ejaculatio Praecoxs", "Praecoxs, Ejaculatio", "praecox; ejaculation", "premature ejaculation", "Premature ejaculation", "ejaculation premature", "Ejaculation premature", "EJACULATION PREMATURE", "Premature Ejaculation", "Premature;ejaculation", "premature; ejaculation", "Ejaculation, premature", "Premature Ejaculations", "ejaculations premature", "Ejaculation, Premature", "ejaculation; premature", "Ejaculations, Premature", "Premature orgasm - male", "Premature ejaculation disorder", "premature ejaculation disorder", "Premature ejaculation (finding)", "premature ejaculation (disease)", "premature ejaculation (symptom)", "premature ejaculation (diagnosis)", "dysfunction; sexual, premature ejaculation", "sexual; functional disturbance, premature ejaculation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "premature ejaculation", "shortest_name_length": 10}
{"curie": "MONDO:0013074", "names": ["ECCL", "Fishman Syndrome", "Fishman syndrome", "Haberland syndrome", "Encephalocraniocutaneous Lipomatosis", "encephalocraniocutaneous lipomatosis", "ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS", "Encephalocraniocutaneous lipomatosis", "ECCL - Encephalocraniocutaneous lipomatosis", "encephalocraniocutaneous lipomatosis (ECCL)", "ECCL - encephalocraniocutaneous lipomatosis", "Encephalocraniocutaneous lipomatosis (disorder)", "encephalocraniocutaneous lipomatosis, somatic mosaic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephalocraniocutaneous lipomatosis", "shortest_name_length": 4}
{"curie": "MONDO:0015743", "names": ["idiopathic bilateral vestibulopathy", "Idiopathic bilateral vestibulopathy", "Idiopathic bilateral vestibulopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic bilateral vestibulopathy", "shortest_name_length": 35}
{"curie": "UMLS:C0151476", "names": ["Hypochloremic alkalosis", "ALKALOSIS HYPOCHLOREMIC", "HYPOCHLOREMIC ALKALOSIS", "Alkalosis hypochloremic", "Alkalosis hypochloraemic", "Hypochloraemic alkalosis", "Hypochloremic alkalosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypochloremic alkalosis", "shortest_name_length": 23}
{"curie": "MONDO:0018861", "names": ["Ahn Lerman Sagie syndrome", "AHN-Lerman-Sagie syndrome", "Ahn-Lerman-Sagie syndrome", "Zellweger-like syndrome without peroxisomal anomaly", "Zellweger-like syndrome without peroxisomal anomalies", "Zellweger-like syndrome without peroxisomal anomaly (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Zellweger-like syndrome without peroxisomal anomalies", "shortest_name_length": 25}
{"curie": "MONDO:0012085", "names": ["CILD3", "Primary Ciliary Dyskinesia 3", "primary ciliary dyskinesia 3", "Primary ciliary dyskinesia, 3", "CILIARY DYSKINESIA, PRIMARY, 3", "Ciliary Dyskinesia, Primary, 3", "ciliary dyskinesia, primary, 3", "DNAH5 primary ciliary dyskinesia", "primary ciliary dyskinesia type 3", "ciliary dyskinesia, primary, type 3", "primary ciliary dyskinesia caused by mutation in DNAH5", "primary ciliary dyskinesia 3 with or without situs inversus", "CILIARY DYSKINESIA, PRIMARY, 3, WITH OR WITHOUT SITUS INVERSUS", "Ciliary Dyskinesia, Primary, 3, with or without Situs Inversus", "ciliary dyskinesia, primary, 3, with or without situs inversus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia 3", "shortest_name_length": 5}
{"curie": "MONDO:0013539", "names": ["LTC4 SYNTHASE DEFICIENCY", "LTC4 Synthase Deficiency", "LTC4 synthase deficiency", "Leukotriene C4 synthase deficiency", "LEUKOTRIENE C4 SYNTHASE DEFICIENCY", "Leukotriene C4 Synthase Deficiency", "leukotriene C4 synthase deficiency", "Deficiency of leukotriene C4 synthase", "Deficiency of leukotriene C4 synthase (disorder)", "hypotonia-failure to thrive-microcephaly syndrome", "Hypotonia-failure to thrive-microcephaly syndrome", "Hypotonia with failure to thrive and microcephaly syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotonia-failure to thrive-microcephaly syndrome", "shortest_name_length": 24}
{"curie": "MONDO:0001919", "names": ["Cystic macular degeneration", "Cystoid macular degeneration", "Cystic degeneration of macula", "Cystic degeneration of the macula", "Cystoid macular retinal degeneration", "cystoid macular retinal degeneration", "macular retinal degeneration cystoid", "cystoid macular degeneration of retina", "Cystoid macular degeneration of retina", "Cystoid macular degeneration (diagnosis)", "Cystoid macular retinal degeneration (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cystoid macular retinal degeneration", "shortest_name_length": 27}
{"curie": "MONDO:0000382", "names": ["Neoplasm benign;respiratory", "Benign respiratory neoplasm", "benign respiratory neoplasm", "Benign neoplasm respiratory", "benign neoplasms respiratory", "Benign Respiratory Tract Neoplasm", "benign neoplasm respiratory system", "respiratory system benign neoplasm", "Benign Respiratory System Neoplasm", "benign neoplasm of respiratory system", "Benign neoplasm of respiratory system", "benign neoplasm of the respiratory system", "Benign neoplasm of respiratory system (disorder)", "benign neoplasm of respiratory system (diagnosis)", "Benign neoplasm of respiratory system, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "respiratory system benign neoplasm", "shortest_name_length": 27}
{"curie": "MONDO:0009431", "names": ["HHRH", "HYPERCALCIURIC RICKETS", "Hypercalciuric rickets", "Hypercalciuric Rickets", "hypercalciuric rickets", "Hypophosphatemic Hypercalciuric Rickets", "hypercalciuric hypophosphatemic rickets", "hypophosphatemic hypercalciuric rickets", "Hypercalciuric Hypophosphatemic Rickets", "hypophosphatemic rickets with hypercalciuria", "Autosomal recessive hypophosphatemic bone disease", "Autosomal recessive hypophosphataemic bone disease", "hereditary hypophosphatemic rickets with hypercalciuria", "Hereditary hypophosphatemic rickets with hypercalciuria", "Hereditary Hypophosphatemic Rickets with Hypercalciuria", "hypophosphatemic rickets with hypercalciuria, hereditary", "HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY", "Hypophosphatemic Rickets with Hypercalciuria, Hereditary", "Hereditary hypophosphataemic rickets with hypercalciuria", "Autosomal recessive hypophosphatemic bone disease (disorder)", "HHRH - Hereditary hypophosphatemic rickets with hypercalciuria", "HHRH - hereditary hypophosphatemic rickets with hypercalciuria", "HHRH - Hereditary hypophosphataemic rickets with hypercalciuria", "HHRH - hereditary hypophosphataemic rickets with hypercalciuria", "Hereditary hypophosphatemic rickets with hypercalciuria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary hypophosphatemic rickets with hypercalciuria", "shortest_name_length": 4}
{"curie": "MONDO:0001687", "names": ["Cataract diabetic", "Diabetic cataract", "diabetic cataract", "cataract diabetic", "cataract - diabetic", "Cataract - diabetic", "diabetic cataract (diagnosis)", "Cataract due to diabetes mellitus", "diabetes; cataract (manifestation)", "cataract; diabetes (manifestation)", "Cataract of eye due to diabetes mellitus", "Cataract of eye due to diabetes mellitus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diabetic cataract", "shortest_name_length": 17}
{"curie": "MONDO:0004512", "names": ["Meningeal Melanomatosis", "meningeal melanomatosis", "Meningeal melanomatosis", "Leptomeningeal Melanomatosis", "leptomeningeal melanomatosis", "Leptomeningeal melanomatosis", "meningeal cluster melanomatosis", "melanomatosis of meningeal cluster", "malignant melanomatosis of meninges", "malignant melanomatosis of meninges (diagnosis)", "meningeal melanomatosis (morphologic abnormality)", "Meningeal melanomatosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "meningeal melanomatosis", "shortest_name_length": 23}
{"curie": "MONDO:0100090", "names": ["CAD due to FGF10", "congenital alveolar dysplasia due to FGF10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital alveolar dysplasia due to FGF10", "shortest_name_length": 16}
{"curie": "MONDO:0007991", "names": ["Kawashima-Tsuji syndrome", "Kawashima Tsuji syndrome", "Kawashima tsuji syndrome", "Microcephaly deafness syndrome", "microcephaly deafness syndrome", "microcephaly-deafness syndrome", "MICROCEPHALY-DEAFNESS SYNDROME", "Microcephaly-Deafness Syndrome", "microcephaly-deafness-intellectual disability syndrome", "Microcephaly-deafness-intellectual disability syndrome", "Microcephaly-hearing loss-intellectual disability syndrome", "microcephaly with deafness and intellectual disability syndrome", "Microcephaly with deafness and intellectual disability syndrome", "Microcephaly with deafness and intellectual disability syndrome (disorder)", "microcephaly with deafness and intellectual disability syndrome (diagnosis)", "Syndrome of microcephaly, deafness-malformed ears, mental retardation and peculiar facies", "syndrome of microcephaly, deafness/malformed ears, mental retardation and peculiar facies", "syndrome of microcephaly, deafness/malformed ears, intellectual disability and peculiar facies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly-deafness-intellectual disability syndrome", "shortest_name_length": 24}
{"curie": "MONDO:0001017", "names": ["epididymis adenocarcinoma", "epididymal adenocarcinoma", "Epididymal Adenocarcinoma", "adenocarcinoma of epididymis", "adenocarcinoma of the epididymis", "Adenocarcinoma of the Epididymis", "adenocarcinoma of epididymis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epididymal adenocarcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0007203", "names": ["BRBN", "BRBNS", "bean syndrome", "BEAN SYNDROME", "Bean syndrome", "Bean Syndrome", "BLUE RUBBER BLEB NEVUS", "Blue Rubber Bleb Nevus", "blue rubber bleb nevus", "Blue rubber bleb nevus", "Blue rubber bleb naevus", "blue rubber bleb nevus syndrome", "Blue rubber bleb nevus syndrome", "Blue rubber bleb naevus syndrome", "Blue rubber bleb nevus (disorder)", "blue rubber bleb nevus syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blue rubber bleb nevus", "shortest_name_length": 4}
{"curie": "UMLS:C4683747", "names": ["Stage IIIB Mycosis Fungoides and Sezary Syndrome AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Mycosis Fungoides and Sezary Syndrome AJCC v8", "shortest_name_length": 56}
{"curie": "MONDO:0007536", "names": ["CLE", "congenital emphysema", "Congenital emphysema", "emphysema congenital", "Emphysema, congenital", "emphysema; congenital", "congenital; emphysema", "infantile lobar emphysema", "Infantile lobar emphysema", "emphysema congenital lobar", "congenital lobar emphysema", "Congenital lobar emphysema", "Congenital Lobar Emphysema", "EMPHYSEMA, CONGENITAL LOBAR", "Emphysema, congenital lobar", "emphysema, congenital lobar", "Congenital lobar overinflation", "Infantile lobar hyperinflation", "infantile lobar hyperinflation", "congenital lobar hyperinflation", "Congenital emphysema (disorder)", "Congenital lobar hyperinflation", "CLE - Congenital lobar emphysema", "Congenital emphysema (diagnosis)", "Congenital lobar emphysema (disorder)", "Congenital lobar emphysema (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital lobar emphysema", "shortest_name_length": 3}
{"curie": "MONDO:0700029", "names": ["partial duplication of chromosome 13"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of chromosome 13", "shortest_name_length": 36}
{"curie": "UMLS:C4331988", "names": ["Stage IVB Oropharyngeal (p16-Negative) Throat Cancer", "Stage IVB Oropharyngeal (p16-Negative) Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Oropharyngeal (p16-Negative) Carcinoma AJCC v8", "shortest_name_length": 52}
{"curie": "UMLS:C1334431", "names": ["Low Risk Gastric GIST", "Low Risk Gastric Gastrointestinal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Risk Gastric Gastrointestinal Stromal Tumor", "shortest_name_length": 21}
{"curie": "MONDO:0008160", "names": ["OSTEOSCLEROSIS WITH ICHTHYOSIS AND FRACTURES", "Osteosclerosis with Ichthyosis and Fractures", "osteosclerosis with ichthyosis and fractures", "CORTICAL THICKENING OF LONG BONES WITH BOWING AND ICHTHYOSIS", "Cortical Thickening of Long Bones with Bowing and Ichthyosis", "cortical thickening of long bones with bowing and ichthyosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteosclerosis with ichthyosis and fractures", "shortest_name_length": 44}
{"curie": "MONDO:0032842", "names": ["SIDDIS", "Siddiqi syndrome", "SIDDIQI SYNDROME", "DEAFNESS, DYSTONIA, DEVELOPMENTAL DELAY, AND POOR GROWTH", "Deafness, Dystonia, Developmental Delay, and Poor Growth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Siddiqi syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C1519714", "names": ["Type II Endometrial Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Type II Endometrial Adenocarcinoma", "shortest_name_length": 34}
{"curie": "UMLS:C0678051", "names": ["Stage II Adrenal Cortex Cancer", "stage II adrenocortical cancer", "Stage II Adrenocortical Carcinoma", "Stage II Adrenal Cortex Carcinoma", "Stage II Carcinoma of Adrenal Cortex", "Stage II Carcinoma of the Adrenal Cortex", "Stage II Adrenal Cortex Carcinoma AJCC v7", "Stage II Adrenal Cortical Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Adrenal Cortex Carcinoma AJCC v7", "shortest_name_length": 30}
{"curie": "UMLS:C5204616", "names": ["Bladder Benign PEComa", "Bladder Benign Perivascular Epithelioid Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder Benign PEComa", "shortest_name_length": 21}
{"curie": "UMLS:C4721666", "names": ["Bladder cancer stage IV", "stage IV bladder cancer", "stage iv bladder cancer", "bladder cancer, stage IV", "metastatic bladder cancer", "bladder cancer, metastatic", "Carcinoma bladder stage IV", "Bladder carcinoma stage IV", "Metastatic Bladder Carcinoma", "stage IV cancer of the bladder", "cancer of the bladder, stage IV", "metastatic cancer of the bladder", "stage IV carcinoma of the bladder", "cancer of the bladder, metastatic", "Carcinoma urinary bladder stage IV", "carcinoma of the bladder, stage IV", "Urinary bladder carcinoma stage IV", "Metastatic carcinoma of the bladder", "metastatic carcinoma of the bladder", "carcinoma of the bladder, metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder cancer stage IV", "shortest_name_length": 23}
{"curie": "MONDO:0018823", "names": ["X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome", "shortest_name_length": 107}
{"curie": "MONDO:0006900", "names": ["Perinephritis", "PERINEPHRITIS", "perinephritis", "Perinephritides", "Perinephritis, NOS", "Perinephritis (disorder)", "Perinephrium Inflammation", "perirenal fat inflammation", "Inflammation, Perinephrium", "Inflammations, Perinephrium", "inflammation of perirenal fat"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "perinephritis", "shortest_name_length": 13}
{"curie": "MONDO:0009839", "names": ["PSP-p", "atypical PSP", "Atypical PSP", "PSP-parkinsonism", "PARKINSON-DEMENTIA SYNDROME", "Parkinson-Dementia Syndrome", "Parkinson-dementia syndrome", "Progressive supranuclear palsy atypical", "progressive supranuclear palsy atypical", "supranuclear palsy, progressive atypical", "Supranuclear Palsy, Progressive Atypical", "Supranuclear Palsy, Progressive, 1, Atypical", "SUPRANUCLEAR PALSY, PROGRESSIVE, 1, ATYPICAL", "supranuclear palsy, progressive, 1, atypical", "Steele-Richardson-Olszewski Syndrome, Atypical", "STEELE-RICHARDSON-OLSZEWSKI SYNDROME, ATYPICAL", "Steele-Richardson-Olszewski syndrome, atypical", "progressive supranuclear palsy-parkinsonism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive supranuclear palsy-parkinsonism syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0025167", "names": ["Avian reticuloendotheliosis", "Avian Reticuloendothelioses", "Avian Reticuloendotheliosis", "reticuloendotheliosis, avian", "Reticuloendothelioses, Avian", "Reticuloendotheliosis, Avian", "Avian reticuloendotheliosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "reticuloendotheliosis, avian", "shortest_name_length": 27}
{"curie": "UMLS:C4553249", "names": ["Stage II Vaginal Cancer", "Stage II Vaginal Cancer AJCC v8", "Stage II Vaginal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Vaginal Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "UMLS:C4726628", "names": ["Metastatic Unresectable Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Unresectable Sarcoma", "shortest_name_length": 31}
{"curie": "MONDO:0004427", "names": ["supraglottic tumor", "supraglottis tumor", "Supraglottic tumor", "Supraglottic Tumor", "Supraglottis Tumor", "Tumor of Supraglottis", "tumor of supraglottis", "Tumor of supraglottis", "Supraglottic Neoplasm", "supraglottis neoplasm", "supraglottic neoplasm", "Supraglottis Neoplasm", "Tumour of supraglottis", "Neoplasm of Supraglottis", "Neoplasm of supraglottis", "neoplasm of supraglottis", "Tumor of the Supraglottis", "tumor of the supraglottis", "Neoplasm of the Supraglottis", "neoplasm of the supraglottis", "laryngeal neoplasm supraglottis", "supraglottic part of larynx tumor", "Neoplasm of supraglottis (disorder)", "neoplasm of supraglottis (diagnosis)", "tumor of supraglottic part of larynx", "supraglottic part of larynx neoplasm", "neoplasm of supraglottic part of larynx", "supraglottic part of larynx neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "supraglottis neoplasm", "shortest_name_length": 18}
{"curie": "UMLS:C5206817", "names": ["Acute Lymphoblastic Leukemia with t(4;11)(q21;23)", "B Acute Lymphoblastic Leukemia with t(4;11)(q21;23)", "B-Cell Acute Lymphoblastic Leukemia with t(4;11)(q21;23)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B Acute Lymphoblastic Leukemia with t(4;11)(q21;23)", "shortest_name_length": 49}
{"curie": "MONDO:0017720", "names": ["GM2 Gangliosidose", "GM2 gangliosidosis", "GM2 Gangliosidoses", "Gangliosidoses GM2", "gangliosidoses gm2", "gangliosidosis GM2", "GM2 Gangliosidosis", "Gangliosidose, GM2", "gm2 gangliosidosis", "gangliosidosis; GM2", "Gangliosidosis, GM2", "GM2; gangliosidosis", "GM2, Gangliosidoses", "Gangliosidoses, GM2", "GM>2< gangliosidosis", "G(M2) Gangliosidoses", "GM2 gangliosidosis, NOS", "GM2 gangliosidosis (disorder)", "gm2 gangliosidosis (diagnosis)", "GM2 gangliosidosis, unspecified", "GM2-gangliosidosis, B, B1, AB variant", "Deficiency of beta-N-acetylhexosaminidase isoenzymes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "GM2 gangliosidosis", "shortest_name_length": 17}
{"curie": "MONDO:0008746", "names": ["OCA2", "BOCA", "Albinism 2", "albinism 2", "Albinoidism", "Albinism II", "ALBINISM II", "Brown albinism", "BROWN OCULOCUTANEOUS ALBINISM", "Brown Oculocutaneous Albinism", "Brown oculocutaneous albinism", "albinism, Brown oculocutaneous", "oculocutaneous albinism type 2", "ALBINISM, BROWN OCULOCUTANEOUS", "Albinism, Brown Oculocutaneous", "Oculocutaneous albinism ty-pos", "Oculocutaneous albinism type 2", "oculocutaneous albinism, type 2", "oculocutaneous albinism type II", "OCULOCUTANEOUS ALBINISM, TYPE II", "albinism, oculocutaneous, type 2", "Albinism, oculocutaneous, type 2", "Oculocutaneous Albinism, Type II", "Albinism, Oculocutaneous, Type II", "albinism, oculocutaneous, type II", "ALBINISM, OCULOCUTANEOUS, TYPE II", "Brown oculocutaneous albinism (disorder)", "oculocutaneous albinism type 2 (diagnosis)", "Oculocutaneous albinism tyrosinase positive", "oculocutaneous albinism tyrosinase-positive", "Tyrosinase-positive oculocutaneous albinism", "tyrosinase-positive oculocutaneous albinism", "oculocutaneous albinism tyrosinase positive", "Tyrosinase positive oculocutaneous albinism", "oculocutaneous albinism, tyrosinase-positive", "OCULOCUTANEOUS ALBINISM, TYROSINASE-POSITIVE", "Oculocutaneous Albinism, Tyrosinase-Positive", "albinism, oculocutaneous, type II, modifier of", "OCA2 - Tyrosinase-positive oculocutaneous albinism", "Tyrosinase-positive oculocutaneous albinism (disorder)", "Tyrosinase-positive oculocutaneous albinism (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculocutaneous albinism type 2", "shortest_name_length": 4}
{"curie": "MONDO:0003111", "names": ["GNET", "Gastric NET", "stomach NET", "NET of stomach", "Gastric neuroendocrine tumor", "stomach neuroendocrine tumor", "Gastric Neuroendocrine Neoplasm", "Gastric neuroendocrine neoplasm", "neuroendocrine tumor of stomach", "Neuroendocrine tumor of stomach", "gastric neuroendocrine neoplasm", "Stomach Neuroendocrine Neoplasm", "stomach neuroendocrine neoplasm", "neuroendocrine neoplasm of stomach", "Neuroendocrine Neoplasm of Stomach", "Neuroendocrine neoplasm of stomach", "neuroendocrine tumor of the stomach", "neuroendocrine neoplasm of the stomach", "Neuroendocrine Neoplasm of the Stomach", "Neuroendocrine neoplasm of stomach (disorder)", "stomach neuroendocrine tumor, well differentiated, low or intermediate grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric neuroendocrine neoplasm", "shortest_name_length": 4}
{"curie": "UMLS:C1335354", "names": ["Parotid Adenocarcinoma", "Adenocarcinoma of Parotid", "Parotid Gland Adenocarcinoma", "Adenocarcinoma of the Parotid", "Adenocarcinoma of Parotid Gland", "adenocarcinoma of parotid gland", "Adenocarcinoma of the Parotid Gland", "malignant parotid neoplasm adenocarcinoma", "adenocarcinoma of parotid gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenocarcinoma of parotid gland", "shortest_name_length": 22}
{"curie": "MONDO:0015545", "names": ["MAS", "macrophage activation syndrome", "Macrophage activation syndrome", "Macrophage Activation Syndrome", "Syndrome, Macrophage Activation", "Reactive hemophagocytic syndrome", "Reactive haemophagocytic syndrome", "Macrophage activation syndrome (disorder)", "macrophage activation syndrome (diagnosis)", "Reactive Hemophagocytic Lymphohistiocytosis", "reactive hemophagocytic lymphohistiocytosis", "Hemophagocytic lymphohistiocytosis with rheumatologic disease", "Haemophagocytic lymphohistiocytosis with rheumatologic disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macrophage activation syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C4287895", "names": ["Broad Ligament Serous Adenofibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Broad Ligament Serous Adenofibroma", "shortest_name_length": 34}
{"curie": "UMLS:C5555526", "names": ["Recurrent Primary Myelofibrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Primary Myelofibrosis", "shortest_name_length": 31}
{"curie": "MONDO:0000343", "names": ["Barmah Forest virus disease", "Barmah forest virus disease", "Barmah Forest virus infectious disease", "Barmah Forest virus disease or disorder", "Barmah Forest virus caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Barmah forest virus disease", "shortest_name_length": 27}
{"curie": "MONDO:0014661", "names": ["EBS5D", "EBSND", "epidermolysis bullosa simplex with nail dystrophy", "EPIDERMOLYSIS BULLOSA SIMPLEX WITH NAIL DYSTROPHY", "EPIDERMOLYSIS BULLOSA SIMPLEX 5D, WITH NAIL DYSTROPHY", "epidermolysis bullosa simplex 5D, generalized intermediate, autosomal recessive", "EPIDERMOLYSIS BULLOSA SIMPLEX 5D, GENERALIZED INTERMEDIATE, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolysis bullosa simplex with nail dystrophy", "shortest_name_length": 5}
{"curie": "UMLS:C2938970", "names": ["Penile curvature"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Penile curvature", "shortest_name_length": 16}
{"curie": "MONDO:0017762", "names": ["Copper Disorders", "metabolic disorder; copper", "Copper metabolism disorder", "copper Transport disorders", "copper metabolism disorder", "copper; metabolic disorder", "Copper metabolism disorders", "disorder of copper metabolism", "Disorder of copper metabolism", "disorders of copper metabolism", "DISORDERS OF COPPER METABOLISM", "Disorders of copper metabolism", "Copper metabolism disorder NOS", "Disorder of copper metabolism, NOS", "copper metabolism disorder (diagnosis)", "Disorder of copper metabolism (disorder)", "Disorder of copper metabolism, unspecified", "inborn cellular copper ion homeostasis disorder", "inborn error of cellular copper ion homeostasis", "rare inborn error of cellular copper ion homeostasis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of copper metabolism", "shortest_name_length": 16}
{"curie": "UMLS:C1963826", "names": ["Mitochondrial enzyme deficiency", "Mitochondrial Enzyme Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mitochondrial enzyme deficiency", "shortest_name_length": 31}
{"curie": "UMLS:C1336355", "names": ["Stage IVA Oropharynx Carcinoma", "Stage IVA Oropharyngeal Carcinoma", "Stage IVA Carcinoma of Oropharynx", "Stage IVA Carcinoma of the Oropharynx", "Stage IVA Oropharyngeal Throat Cancer", "Stage IVA Oropharyngeal Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Oropharyngeal Carcinoma AJCC v7", "shortest_name_length": 30}
{"curie": "UMLS:C4682578", "names": ["Uterine Corpus Adenosarcoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Corpus Adenosarcoma by AJCC v8 Stage", "shortest_name_length": 44}
{"curie": "MONDO:0009389", "names": ["HYPERLYSINEMIA DUE TO DEFECT IN LYSINE TRANSPORT INTO MITOCHONDRIA", "Hyperlysinemia Due To Defect In Lysine Transport Into Mitochondria", "hyperlysinemia due to defect in lysine TRANSPORT into mitochondria", "hyperlysinemia due to defect in lysine transport into mitochondria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperlysinemia due to defect in lysine transport into mitochondria", "shortest_name_length": 66}
{"curie": "MONDO:0006848", "names": ["Marcor", "MARASMUS", "Marasmus", "marasmus", "Athrepsia", "athrepsia", "Pedatrophy", "Pedatrophia", "Marantic atrophy", "Infantile atrophy", "Marasmus infantilis", "severe malnutrition", "Marasmus lactantium", "nutritional atrophy", "Severe malnutrition", "Nutritional atrophy", "malnutrition severe", "malnutrition; severe", "Nutritional marasmus", "marasmus (diagnosis)", "nutritional marasmus", "severe; malnutrition", "malnutrition; marasmus", "Severe malnutrition NOS", "Severe malnutrition, NOS", "Primary infantile atrophy", "Parrot atrophy of the newborn", "severe; malnutrition, marasmus", "malnutrition; severe, marasmus", "Nutritional marasmus (disorder)", "Severe malnutrition with marasmus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "marasmus", "shortest_name_length": 6}
{"curie": "MONDO:0011993", "names": ["ASPIRIN RESISTANCE", "aspirin resistance", "aspirin, resistance to Antithrombotic Effect of", "ASPIRIN, RESISTANCE TO ANTITHROMBOTIC EFFECT OF", "ASPIRIN, RESISTANCE TO CARDIOPROTECTIVE EFFECT OF", "aspirin, resistance to Cardioprotective Effect of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aspirin resistance", "shortest_name_length": 18}
{"curie": "MONDO:0004885", "names": ["choroid; sclerosis", "sclerosis; choroid", "choroidal sclerosis", "Choroidal sclerosis", "CHOROIDAL SCLEROSIS", "choroid; degeneration", "degeneration; choroid", "choroidal degeneration", "Choroidal degeneration", "choroidal degenerations", "Choroidal sclerosis NOS", "Choroidal degenerations", "Choroidal sclerosis, NOS", "Choroidal vessel sclerosis", "choroidopathy; degenerative", "Choroidal degeneration, NOS", "degenerative; choroidopathy", "Choroidal sclerosis (finding)", "Choroidal degeneration (disorder)", "choroidal degeneration (diagnosis)", "Unspecified choroidal degeneration", "Choroidal degeneration, unspecified", "optic choroid neurodegenerative disease", "neurodegenerative disease of optic choroid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choroidal sclerosis", "shortest_name_length": 18}
{"curie": "MONDO:0014994", "names": ["GDACCF", "global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies", "GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES", "global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies; GDACCF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies", "shortest_name_length": 6}
{"curie": "UMLS:C0751088", "names": ["Medication-Induced Dyskinesia", "Medication Induced Dyskinesia", "Dyskinesia, Medication Induced", "Dyskinesia, Medication-Induced", "Medication-Induced Dyskinesias", "Dyskinesias, Medication-Induced"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dyskinesia, Medication-Induced", "shortest_name_length": 29}
{"curie": "MONDO:0018315", "names": ["X-linked osteoporosis with fractures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked osteoporosis with fractures", "shortest_name_length": 36}
{"curie": "MONDO:0014042", "names": ["LVNC7", "left ventricular noncompaction 7", "Left Ventricular Noncompaction 7", "LEFT VENTRICULAR NONCOMPACTION 7", "MIB1 left ventricular noncompaction", "left ventricular noncompaction type 7", "left ventricular noncompaction caused by mutation in MIB1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "left ventricular noncompaction 7", "shortest_name_length": 5}
{"curie": "MONDO:0008105", "names": ["POTATO NOSE", "potato Nose", "Potato nose", "bulbous nose", "Bulbous nose", "NOSE BULBOUS", "Bulbous nasal tip", "Nose, anomalous shape of", "nose, anomalous shape of", "NOSE, ANOMALOUS SHAPE OF", "bulbous nose (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nose, anomalous shape of", "shortest_name_length": 11}
{"curie": "UMLS:C5574657", "names": ["ventricular tachyarrhythmia", "VENTRICULAR TACHYARRHYTHMIA", "Ventricular tachyarrhythmia", "Ventricular tachyarrhythmias", "Ventricular tachyarrhythmia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ventricular tachyarrhythmia", "shortest_name_length": 27}
{"curie": "UMLS:C1096176", "names": ["Mitochondrial Damage", "Mitochondrial toxicity", "Mitochondrial Toxicity", "mitochondrial toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mitochondrial toxicity", "shortest_name_length": 20}
{"curie": "UMLS:C0263477", "names": ["female pattern alopecia", "female pattern baldness", "Female pattern baldness", "baldness female pattern", "Female pattern alopecia", "Female Pattern Baldness", "Baldness, Female Pattern", "baldness females pattern", "baldness female patterned", "Female pattern alopecia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Female pattern alopecia (disorder)", "shortest_name_length": 23}
{"curie": "UMLS:C0852685", "names": ["Abnormal palmar/plantar creases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abnormal palmar/plantar creases", "shortest_name_length": 31}
{"curie": "MONDO:0000466", "names": ["1st degree av block", "AV block-1st degree", "First Degree AV Block", "AV Block First Degree", "first degree av block", "av first degree block", "first degree AV block", "AV block first degree", "AV BLOCK FIRST DEGREE", "First degree AV block", "first degree A-V block", "Heart block 1st degree", "1st degree heart block", "A-V block first degree", "FIRST DEGREE HEART BLOCK", "block degree first heart", "Heart block first degree", "HEART BLOCK FIRST DEGREE", "First degree heart block", "first degree heart block", "block; heart, first degree", "First-degree AV heart block", "HEART BLOCK AV FIRST DEGREE", "Heart block AV first degree", "first degree atrioventricular block", "First-degree atrioventricular block", "Atrioventricular block first degree", "First Degree Atrioventricular Block", "first-degree atrioventricular block", "First degree atrioventricular block", "atrioventricular block first degree", "atrioventricular block, first degree", "Atrioventricular block, first degree", "Atrioventricular block, first-degree", "Atrioventricular Block, First Degree", "block; atrioventricular, first degree", "First-degree atrioventricular heart block", "Atrioventricular conduction time prolonged", "First degree atrioventricular block (disorder)", "Incomplete atrioventricular block, first degree", "first degree atrioventricular block (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "first-degree atrioventricular block", "shortest_name_length": 19}
{"curie": "MONDO:0001733", "names": ["Venous tributary (branch) occlusion", "Venous tributary occlusion of retina", "venous tributary occlusion of retina", "occlusion of tributary of retinal vein", "Venous tributary branch occlusion of retina", "venous tributary branch occlusion of retina", "venous tributary (branch) occlusion of retina", "Venous tributary (branch) occlusion of retina"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "occlusion of tributary of retinal vein", "shortest_name_length": 35}
{"curie": "UMLS:C0948112", "names": ["Chest Wall Cyst", "Chest wall cyst", "chest wall cyst", "chest cyst wall"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chest wall cyst", "shortest_name_length": 15}
{"curie": "MONDO:0006528", "names": ["bacterial exanthem"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bacterial exanthem", "shortest_name_length": 18}
{"curie": "MONDO:0023670", "names": ["BBS20", "Bardet-Biedl syndrome 20"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bardet-Biedl syndrome 20", "shortest_name_length": 5}
{"curie": "MONDO:0017867", "names": ["distal del(17)(p13.1)", "distal 17p13.1 microdeletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal 17p13.1 microdeletion syndrome", "shortest_name_length": 21}
{"curie": "MONDO:0013068", "names": ["ARHI2", "Presbycusis 2", "presbycusis 2", "PRESBYCUSIS 2", "age-related hearing impairment 2", "AGE-RELATED HEARING IMPAIRMENT 2", "Age-Related Hearing Impairment 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "age-related hearing impairment 2", "shortest_name_length": 5}
{"curie": "MONDO:0030046", "names": ["NEDBASS", "NEURODEVELOPMENTAL DISORDER AND STRUCTURAL BRAIN ANOMALIES WITH OR WITHOUT SEIZURES AND SPASTICITY", "neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity", "shortest_name_length": 7}
{"curie": "UMLS:C4727195", "names": ["Locally Advanced Digestive System Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Digestive System Carcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0010835", "names": ["khalifa-Graham syndrome", "Khalifa-Graham syndrome", "Khalifa Graham syndrome", "Pterygium colli mental retardation digital anomalies", "pterygium colli mental retardation digital anomalies", "pterygium colli intellectual disability digital anomalies", "Pterygium colli-intellectual disability-digital anomalies syndrome", "pterygium colli-intellectual disability-digital anomalies syndrome", "PTERYGIUM COLLI AND MENTAL RETARDATION WITH FACIAL AND DIGITAL ANOMALIES", "pterygium colli and mental retardation with facial and digital anomalies", "Pterygium colli and mental retardation with facial and digital anomalies", "Pterygium colli with intellectual disability and digital anomaly syndrome", "pterygium colli and intellectual disability with facial and digital anomalies", "Pterygium colli with intellectual disability and digital anomaly syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pterygium colli-intellectual disability-digital anomalies syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0010481", "names": ["Quincke", "ANGIOEDEMA", "angioedema", "Angioedema", "Hives giant", "Angiooedema", "angio edema", "Angioedemas", "Giant hives", "giant hives", "angioedemas", "GIANT HIVES", "ANGIO-EDEMA", "HIVES GIANT", "Angio-edema", "angio oedema", "Angio-oedema", "Quincke Edema", "Quincke edema", "quincke edema", "Quincke; edema", "edema; Quincke", "Quinckes Edema", "Quinckes edema", "Quincke oedema", "Edema Quincke's", "giant urticaria", "Urticaria giant", "Quincke's edema", "quincke's edema", "URTICARIA GIANT", "Giant Urticaria", "GIANT URTICARIA", "EDEMA QUINCKE'S", "QUINCKE'S EDEMA", "Quincke's Edema", "Giant urticaria", "Angioedema, NOS", "giant; urticaria", "Quincke's oedema", "Oedema Quincke's", "Urticaria, Giant", "Giant Urticarias", "URTICARIA, GIANT", "urticaria; giant", "urticaria, giant", "QUINCKE'S OEDEMA", "Edema, Quincke's", "QUINCKE SYNDROME", "giant Urticarias", "edema, Quincke's", "BANNISTER DISEASE", "Urticarias, giant", "Quincke's disease", "quincke's disease", "Urticarias, Giant", "Edema angioneurotic", "Angioneurotic Edema", "angioneurotic edema", "Angioneurotic edema", "ANGIONEUROTIC EDEMA", "EDEMA ANGIONEUROTIC", "EDEMA, CIRCUMSCRIBED", "edema, angioneurotic", "angioedema urticaria", "angioneurotic Edemas", "Edema, Angioneurotic", "urticaria angioedema", "angioneurotic oedema", "ANGIONEUROTIC OEDEMA", "Oedema;angioneurotic", "Angioneurotic oedema", "edema; circumscribed", "Oedema angioneurotic", "circumscribed; edema", "angioneurotic; edema", "Angioneurotic Edemas", "edema; angioneurotic", "Edemas, angioneurotic", "Angio-edema-urticaria", "Edemas, Angioneurotic", "Angioedema (disorder)", "Urticaria-angio-edema", "Urticaria-angio-oedema", "angioedema (diagnosis)", "angio oedema urticaria", "Angio-oedema-urticaria", "Angioneurotic edema, NOS", "Angioedema and urticaria", "Angioneurotic oedema, NOS", "Non-histaminic angioedema", "Giant urticaria (disorder)", "MILTON-QUINCKE GIANT URTICARIA", "Bradykinine-induced angioedema", "Non histamine-induced angioedema", "Angioedema (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angioedema", "shortest_name_length": 7}
{"curie": "UMLS:C0814152", "names": ["hepatitis g", "Hepatitis G", "hepatitis G", "Hepatitis G Infection", "hepatitis G infection", "Viral hepatitis, type G", "viral hepatitis G infection", "hepatitis G infection (diagnosis)", "Viral hepatitis, type G (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Viral hepatitis, type G", "shortest_name_length": 11}
{"curie": "MONDO:0004418", "names": ["Microcystic urothelial carcinoma", "microcystic variant infiltrating bladder urothelial carcinoma", "Infiltrating Bladder Urothelial Carcinoma, Microcystic Variant", "infiltrating bladder urothelial carcinoma, microcystic variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcystic variant infiltrating bladder urothelial carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0011929", "names": ["Del(1)(p36)", "Monosomy 1p36", "monosomy 1p36", "deletion 1p36", "Deletion 1p36", "Monosomy 1pter", "deletion 1pter", "Deletion 1pter", "monosomy 1pter", "Distal monosomy 1p36", "MONOSOMY 1p36 SYNDROME", "1p36 Deletion Syndrome", "monosomy 1P36 syndrome", "1p36 deletion syndrome", "Monosomy 1p36 syndrome", "Subtelomeric 1p36 deletion", "subtelomeric 1p36 deletion", "1p36 microdeletion syndrome", "1p Telomere Deletion Syndrome", "1p telomere deletion syndrome", "Chromosome 1p36 deletion syndrome", "Chromosome 1p36 Deletion Syndrome", "chromosome 1p36 deletion syndrome", "Chromosome 1, 1p36 deletion syndrome", "CHROMOSOME 1p36 DELETION SYNDROME, DISTAL", "Chromosome 1p36 deletion syndrome (disorder)", "chromosome 1p36 deletion syndrome, distal, isolated cases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 1p36 deletion syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0000602", "names": ["blood autoimmune disease", "autoimmune disease of blood", "autoimmune disorder of blood", "blood hypersensitivity reaction type II disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune disorder of blood", "shortest_name_length": 24}
{"curie": "MONDO:0006987", "names": ["subaortic stenosis", "Subvalvar stenosis", "Subaortic stenosis", "stenosis; subaortic", "subaortic; stenosis", "subvalvular stenosis", "Subvalvular stenosis", "Aortic Subvalvular Stenoses", "Subvalvular Aortic Stenosis", "Subvalvular Aortic Stenoses", "subvalvular aortic stenosis", "Subvalvular aortic stenosis", "Aortic Subvalvular Stenosis", "Subvalvular Stenoses, Aortic", "Stenosis, Subvalvular Aortic", "Stenosis, Aortic Subvalvular", "Aortic Stenosis, Subvalvular", "Aortic Stenoses, Subvalvular", "Stenoses, Subvalvular Aortic", "Subvalvular Stenosis, Aortic", "Stenoses, Aortic Subvalvular", "Subaortic stenosis (disorder)", "Subvalvular aorta constricted", "Narrowing of blood vessel below aortic heart valve"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subvalvular aortic stenosis", "shortest_name_length": 18}
{"curie": "MONDO:0007854", "names": ["KWE", "Oudtshoorn skin", "Oudtshoorn disease", "Oudtshoorn skin disease", "OUDTSHOORN SKIN DISEASE", "Winter erythrokeratolysis", "Keratolytic winter erythema", "Erythrokeratolysis hiemalis", "keratolytic WINTER erythema", "keratolytic winter erythema", "KERATOLYTIC WINTER ERYTHEMA", "Keratolytic winter erythema (disorder)", "Erythrokeratolysis hiemalis ichthyosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratolytic winter erythema", "shortest_name_length": 3}
{"curie": "MONDO:0020751", "names": ["ORTHYP2", "orthostatic hypotension 2", "ORTHOSTATIC HYPOTENSION 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orthostatic hypotension 2", "shortest_name_length": 7}
{"curie": "MONDO:0001371", "names": ["pcm", "pcms", "Protein-energy malnutrition", "energy malnutrition protein", "protein energy malnutrition", "Protein Energy Malnutrition", "Protein energy malnutrition", "Protein-Energy Malnutrition", "protein-energy malnutrition", "protein-calorie malnutrition", "Malnutrition, Protein-Energy", "protein calorie malnutrition", "Protein Calorie Malnutrition", "Protein-Calorie Malnutrition", "calorie malnutrition protein", "Protein-calorie malnutrition", "Malnutrition protein-calorie", "Deficiency of macronutrients", "Protein calorie malnutrition", "Malnutritions, Protein-Energy", "Malnutrition, Protein-Calorie", "malnutrition; protein, caloric", "Protein-calorie undernutrition", "protein; malnutrition, caloric", "Protein-energy malnutrition, NOS", "Protein-calorie malnutrition, NOS", "PEM - Protein-energy malnutrition", "PCM - Protein-calorie malnutrition", "Deficiency of macronutrients (disorder)", "Unspecified protein-energy malnutrition", "Unspecified protein-calorie malnutrition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "protein-energy malnutrition", "shortest_name_length": 3}
{"curie": "UMLS:C5447337", "names": ["PIK3R1 Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PIK3R1 Deficiency", "shortest_name_length": 17}
{"curie": "MONDO:0017937", "names": ["autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain", "shortest_name_length": 81}
{"curie": "MONDO:0025149", "names": ["Mad cow disease", "Mad cow diseases", "bovine spongiform encephalitis", "encephalitis, bovine spongiform", "bovine spongiform encephalopathy", "Encephalopathy, Bovine Spongiform", "spongiform encephalopathy, bovine", "encephalopathy, bovine spongiform", "BSE (bovine spongiform encephalopathy)", "BSEs (bovine spongiform encephalopathy)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephalopathy, bovine spongiform", "shortest_name_length": 15}
{"curie": "UMLS:C1519825", "names": ["Urethral Glandular Metaplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urethral Glandular Metaplasia", "shortest_name_length": 29}
{"curie": "UMLS:C4054401", "names": ["Nephrotic Syndrome - ACTN4 Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - ACTN4 Associated", "shortest_name_length": 37}
{"curie": "MONDO:0015050", "names": ["esophageal duplication cyst", "Esophageal duplication cyst", "Oesophageal duplication cyst", "Duplication cyst of esophagus", "Duplication cyst of esophagus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophageal duplication cyst", "shortest_name_length": 27}
{"curie": "MONDO:0008806", "names": ["Johnson-Munson syndrome", "Johnson Munson syndrome", "APHALANGY WITH HEMIVERTEBRAE", "Aphalangy with Hemivertebrae", "APHALANGY with hemivertebrae", "Aphalangy-hemivertebrae-urogenital-intestinal dysgenesis syndrome", "Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome", "Aphalangy of the hands and feet, hemivertebrae, and visceral malformations", "Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aphalangy-hemivertebrae-urogenital-intestinal dysgenesis syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0004841", "names": ["Renal hypertrophy", "Renal Hypertrophy", "renal Hypertrophy", "renal hypertrophy", "kidney hypertrophy", "hypertrophy; kidney", "Hypertrophic;kidney", "hypertrophic kidney", "kidney; hypertrophy", "Hypertrophy of kidney", "hypertrophy of kidney", "Hypertrophy of the Kidney", "hypertrophy of the kidney", "Hypertrophy of kidney (disorder)", "hypertrophy of kidney (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kidney hypertrophy", "shortest_name_length": 17}
{"curie": "UMLS:C4688332", "names": ["Recurrent BRCA-Mutated Ovarian Cancer", "Recurrent BRCA-Mutated Ovarian Carcinoma", "Recurrent BRCA- Associated Ovarian Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent BRCA- Associated Ovarian Carcinoma", "shortest_name_length": 37}
{"curie": "UMLS:C4331425", "names": ["Transcription Factor-Associated Monogenic Diabetes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transcription Factor-Associated Monogenic Diabetes", "shortest_name_length": 50}
{"curie": "MONDO:0004368", "names": ["Sphenoorbital Meningioma", "sphenoorbital meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sphenoorbital meningioma", "shortest_name_length": 24}
{"curie": "MONDO:0003593", "names": ["Breast Liposarcoma", "breast liposarcoma", "Liposarcoma of Breast", "liposarcoma of breast", "liposarcoma of the breast", "Liposarcoma of the Breast", "Liposarcoma of the breast", "liposarcoma of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast liposarcoma", "shortest_name_length": 18}
{"curie": "MONDO:0005830", "names": ["Lumpy skin disease", "Lumpy Skin Disease", "lumpy skin disease", "Lumpy Skin Diseases", "Disease, Lumpy Skin", "Skin Disease, Lumpy", "Diseases, Lumpy Skin", "Skin Diseases, Lumpy", "Lumpy skin disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lumpy skin disease", "shortest_name_length": 18}
{"curie": "UMLS:C1334554", "names": ["Male Non-Neoplastic Reproductive System Disease", "Male Non-Neoplastic Reproductive System Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Male Non-Neoplastic Reproductive System Disorder", "shortest_name_length": 47}
{"curie": "MONDO:0002447", "names": ["UCEC", "endometrium ca", "Endometrial Ca", "endometrial ca", "ENDOMETRIUM CANCER", "endometrium cancer", "Endometrial cancer", "endometrial cancer", "Endometrial Cancer", "Endometrium Cancer", "ENDOMETRIAL CANCER", "Cancer, Endometrium", "Cancer, Endometrial", "Endometrium Cancers", "endometrial cancers", "Endometrial Cancers", "Endometrium--Cancer", "Cancers, Endometrium", "Cancers, Endometrial", "Carcinoma endometrial", "CARCINOMA ENDOMETRIAL", "Carcinoma;endometrial", "Endometrial Carcinoma", "endometrial carcinoma", "Cancer of endometrium", "cancer of endometrium", "Cancer of Endometrium", "ENDOMETRIAL CARCINOMA", "Endometrial carcinoma", "Endometrium Carcinoma", "endometrium carcinoma", "Endometrial cancer NOS", "Endometrial Carcinomas", "Endometrium Carcinomas", "Carcinoma, Endometrial", "endometrioid carcinoma", "ENDOMETRIUM, CARCINOMA", "Carcinomas, Endometrial", "CARCINOMA OF ENDOMETRIUM", "carcinoma of endometrium", "Carcinoma of Endometrium", "Cancer of the Endometrium", "cancer of the endometrium", "uterine endometrial cancer", "ENDOMETRIAL CARCINOMA (NOS)", "Carcinoma of the Endometrium", "carcinoma of the Endometrium", "carcinoma of the endometrium", "endometrial carcinoma (disease)", "Endometrial carcinoma (disorder)", "Endometrial carcinoma (diagnosis)", "CARCINOMA, ENDOMETRIAL, MALIGNANT", "carcinoma, endometrial, malignant", "Uterine Corpus Endomential Carcinoma", "UTERINE ENDOMETRIAL CANCER, CARCINOMA", "endometrioid carcinoma of female Reproductive system", "uterine neoplasm, malignant - of endometrium carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometrial carcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0035511", "names": ["ricin poisoning"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ricin poisoning", "shortest_name_length": 15}
{"curie": "MONDO:0009868", "names": ["GSD9B", "GSD IXB", "GSD IXb", "GSD type 9B", "GSD type IXb", "Glycogenosis type 9B", "glycogenosis type 9B", "glycogenosis type IXb", "Glycogenosis type IXb", "Glycogen Storage Disease IXB", "GLYCOGEN STORAGE DISEASE IXb", "glycogen storage disease IXb", "PHKB glycogen storage disease", "Glycogen storage disease type 9B", "glycogen storage disease type 9B", "Glycogen storage disease type IXB", "glycogen storage disease type IXb", "Glycogen storage disease type IXb", "Glycogen storage disease, type IXB", "Glycogen storage disease type IXB (disorder)", "PHKB-related glycogen storage disease type IX", "glycogen storage disease caused by mutation in PHKB", "GLYCOGENOSIS OF LIVER AND MUSCLE, AUTOSOMAL RECESSIVE", "Glycogenosis Of Liver And Muscle, Autosomal Recessive", "glycogenosis of liver and muscle, autosomal recessive", "GSD due to liver and muscle phosphorylase kinase deficiency", "glycogenosis due to liver and muscle phosphorylase kinase deficiency", "Glycogenosis due to liver and muscle phosphorylase kinase deficiency", "Phosphorylase Kinase Deficiency Of Liver And Muscle, Autosomal Recessive", "PHOSPHORYLASE KINASE DEFICIENCY OF LIVER AND MUSCLE, AUTOSOMAL RECESSIVE", "phosphorylase kinase deficiency of liver and muscle, autosomal recessive", "glycogen storage disease due to liver and muscle phosphorylase kinase deficiency", "Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency", "Glycogen storage disease due to liver and muscle glycogen phosphorylase kinase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease IXb", "shortest_name_length": 5}
{"curie": "MONDO:0004653", "names": ["aCML", "Atypical CML", "atypical CML", "Subacute myeloid leukemia", "Subacute Myeloid Leukemia", "subacute myeloid leukemia", "Subacute myelogenous leukemia", "subacute myelogenous leukemia", "Subacute Myelogenous Leukemia", "Subacute granulocytic leukemia", "Subacute Granulocytic Leukemia", "subacute granulocytic leukemia", "atypical chronic myeloid leukemia", "Atypical Chronic Myeloid Leukemia", "atypical chronic myeloid leukaemia", "atypical chronic myeloid leukemia BCR-ABL1 negative", "Atypical Chronic Myeloid Leukemia, BCR-ABL1 Negative", "atypical chronic myeloid leukaemia BCR-ABL1 negative", "atypical chronic myeloid leukemia, BCR-ABL1 negative", "atypical chronic myeloid leukemia, BCR-ABL1 Negative"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical chronic myeloid leukemia, BCR-ABL1 negative", "shortest_name_length": 4}
{"curie": "MONDO:0009221", "names": ["PFFD", "FFU complex", "Ffu syndrome", "FFU SYNDROME", "femur-fibula-ulna complex", "Femur fibula ulna complex", "Femur-fibula-ulna complex", "Femur fibula ulna syndrome", "Femur-fibula-ulna syndrome", "Femur-Fibula-Ulna Syndrome", "femur fibula ulna syndrome", "FEMUR-FIBULA-ULNA SYNDROME", "femur-fibula-ulna syndrome", "Femur-fibula-ulna dysostosis", "femur-fibula-ulna dysostosis", "FFU (femur, fibula, ulna) complex", "Femur fibula ulna complex (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "femur-fibula-ulna complex", "shortest_name_length": 4}
{"curie": "MONDO:0019920", "names": ["UPD(5)pat", "paternal uniparental disomy of chromosome 5", "paternal uniparental disomy of chromosome type 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paternal uniparental disomy of chromosome 5", "shortest_name_length": 9}
{"curie": "UMLS:C2981401", "names": ["Stage IIIA Colorectal Cancer", "Stage IIIA Colorectal Cancer AJCC v7", "Stage IIIA Colorectal (Colon or Rectal) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Colorectal Cancer AJCC v7", "shortest_name_length": 28}
{"curie": "OMIM:212060", "names": ["CARBIMAZOLE SENSITIVITY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 23}
{"curie": "UMLS:C5555531", "names": ["Ovarian Signet Ring Cell Carcinoma", "Ovarian Signet-Ring Cell Carcinoma", "Primary Ovarian Signet Ring Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Signet Ring Cell Carcinoma", "shortest_name_length": 34}
{"curie": "UMLS:C3829188", "names": ["Stage I", "Masaoka Stage I", "Masaoka-Koga Stage I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Masaoka-Koga Stage I", "shortest_name_length": 7}
{"curie": "UMLS:C1282908", "names": ["De Vaal syndrome", "De Vaal's syndrome", "De Vaal's syndrome (disorder)", "De Vaal's syndrome (diagnosis)", "Immunodeficiency with generalized hematopoietic hypoplasia", "Immunodeficiency with generalized haematopoietic hypoplasia", "Immunodeficiency with generalised haematopoietic hypoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "De Vaal's syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0003720", "names": ["Renal Fibrosarcoma", "renal fibrosarcoma", "Kidney Fibrosarcoma", "kidney fibrosarcoma", "KIDNEY, FIBROSARCOMA", "Fibrosarcoma of Kidney", "fibrosarcoma of kidney", "fibrosarcoma of the kidney", "Fibrosarcoma of the kidney", "Fibrosarcoma of the Kidney", "kidney fibrosarcoma (disease)", "fibrosarcoma of kidney (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kidney fibrosarcoma", "shortest_name_length": 18}
{"curie": "MONDO:0000875", "names": ["M5b Adult Acute Leukemia", "M5b adult acute leukemia", "Acute Monocytic Leukemia", "acute monocytic leukemia", "adult acute M5b leukemia", "M5b leukemia, adult acute", "adult acute monocytic leukemia", "Adult Acute Monocytic Leukemia", "acute monocytic leukemia of adults", "adult acute monocytic leukemia (M5b)", "adult acute differentiated M5b leukemia", "M5b leukemia, adult acute differentiated", "adult acute differentiated monoblastic leukemia", "acute differentiated monoblastic leukemia, adult", "monoblastic leukemia, adult acute differentiated", "leukemia, adult acute differentiated monoblastic", "M5b Adult Acute Differentiated Monocytic Leukemia", "M5b adult acute differentiated monocytic leukemia", "adult acute differentiated monocytic leukemia (M5b)", "Adult Acute Differentiated Monocytic Leukemia (M5b)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult acute monocytic leukemia", "shortest_name_length": 24}
{"curie": "MONDO:0006151", "names": ["Colon dysplasia", "dysplasia colon", "colon dysplasia", "Colon Dysplasia", "Colonic Dysplasia", "colonic dysplasia", "dysplasia of colon", "Dysplasia of colon", "Dysplasia of Colon", "Dysplasia of the Colon", "dysplasia of the colon", "Dysplasia of large intestine", "Dysplasia of colon (disorder)", "Dysplasia of large intestine (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colon dysplasia", "shortest_name_length": 15}
{"curie": "UMLS:C2983721", "names": ["Hypopharyngeal Carcinoma by AJCC v6 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypopharyngeal Carcinoma by AJCC v6 Stage", "shortest_name_length": 41}
{"curie": "MONDO:0032654", "names": ["HIES3", "hyper IgE recurrent infection syndrome 3", "hyper-IgE recurrent infection syndrome 3, autosomal recessive", "HYPER-IgE RECURRENT INFECTION SYNDROME 3, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyper-IgE recurrent infection syndrome 3, autosomal recessive", "shortest_name_length": 5}
{"curie": "UMLS:C0038579", "names": ["Intravenous Substance Abuse", "Substance Abuse, Intravenous"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Substance Abuse, Intravenous", "shortest_name_length": 27}
{"curie": "MONDO:0021386", "names": ["mediastinal tumor", "mediastinum tumor", "Mediastinal Tumor", "mediastinum neoplasm", "tumor of mediastinum", "Mediastinal Neoplasm", "mediastinal neoplasm", "Tumor of Mediastinum", "neoplasm of mediastinum", "Neoplasm of Mediastinum", "Tumor of the Mediastinum", "Mediastinal Neoplasm NOS", "tumor of the mediastinum", "Neoplasm of the Mediastinum", "neoplasm of the mediastinum", "mediastinum neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplasm of mediastinum", "shortest_name_length": 17}
{"curie": "MONDO:0012946", "names": ["MRD3", "autosomal dominant mental retardation 3", "Mental Retardation, Autosomal Dominant 3", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 3", "mental retardation, autosomal dominant 3", "autosomal dominant intellectual disability 3", "intellectual disability, autosomal dominant 3", "mental retardation, autosomal dominant type 3", "intellectual disability, autosomal dominant type 3", "autosomal dominant intellectual developmental disorder 3", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 3", "autosomal dominant non-syndromic intellectual disability 3", "CDH15 autosomal dominant non-syndromic intellectual disability", "autosomal dominant non-syndromic intellectual disability caused by mutation in CDH15"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 3", "shortest_name_length": 4}
{"curie": "MONDO:0002764", "names": ["USCC", "Urethra Epidermoid Carcinoma", "urethra epidermoid carcinoma", "urethral squamous cell cancer", "Urethral Squamous Cell Cancer", "Urethral Epidermoid Carcinoma", "urethral Epidermoid carcinoma", "urethral epidermoid carcinoma", "urethra squamous cell carcinoma", "Urethra Squamous Cell Carcinoma", "epidermoid carcinoma of urethra", "Epidermoid Carcinoma of Urethra", "urethral squamous cell carcinoma", "Urethral Squamous Cell Carcinoma", "squamous cell carcinoma of urethra", "Squamous Cell Carcinoma of Urethra", "Epidermoid Carcinoma of the Urethra", "epidermoid carcinoma of the urethra", "squamous cell carcinoma of the urethra", "Squamous Cell Carcinoma of the Urethra", "squamous cell carcinoma of urethra (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urethra squamous cell carcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0009689", "names": ["FIM", "CMS6", "CMS1A", "FIMG2", "CMSEA", "CMS-ea", "CMS1A2", "CMS Ia2", "Cms Ia2", "FIM, FORMERLY", "FIM, formerly", "FIMG2, formerly", "FIMG2, FORMERLY", "CMS1A2, formerly", "FIMG2 (formerly)", "CMS1A2, FORMERLY", "CMS Ia2, FORMERLY", "Cms Ia2, formerly", "CMS Ia2, formerly", "CMS w/episodic apnea", "Myasthenia familial infantile", "familial infantile myasthenia", "Familial infantile myasthenia", "myasthenia familial infantile", "Myasthenia, Familial Infantile", "myasthenia, familial infantile", "congenital myasthenic syndrome 6", "CHAT congenital myasthenic syndrome", "FIM - Familial infantile myasthenia", "congenital myasthenic syndrome type 6", "familial infantile myasthenia gravis 2", "Congenital Myasthenic Syndrome Type Ia", "Congenital myasthenic syndrome type 1a", "congenital myasthenic syndrome type 1a", "congenital myasthenic syndrome type Ia", "congenital myasthenic syndrome type Ia2", "MYASTHENIA, FAMILIAL INFANTILE, FORMERLY", "Familial infantile myasthenia (disorder)", "myasthenia, familial infantile, formerly", "myasthenia gravis, familial infantile, 2", "presynaptic congenital myasthenic syndrome 6", "Presynaptic Congenital Myasthenic Syndrome 6", "congenital myasthenic syndrome 6, presynaptic", "MYASTHENIC SYNDROME, CONGENITAL, 6, PRESYNAPTIC", "myasthenic syndrome, congenital, 6, presynaptic", "congenital myasthenic syndrome type Ia2, formerly", "myasthenia gravis familial infantile 2 (formerly)", "CONGENITAL MYASTHENIC SYNDROME TYPE Ia2, FORMERLY", "MYASTHENIA GRAVIS, FAMILIAL INFANTILE, 2, FORMERLY", "Congenital myasthenic syndrome with episodic apnea", "myasthenia gravis, familial infantile, 2, formerly", "congenital myasthenic syndrome with episodic apnea", "congenital myasthenic syndrome caused by mutation in CHAT", "Myasthenic syndrome congenital associated with episodic apnea", "myasthenic syndrome congenital associated with episodic apnea", "Myasthenic Syndrome, Congenital, Associated With Episodic Apnea", "myasthenic syndrome, congenital, associated with episodic apnea", "congenital presynaptic myasthenic syndrome associated with episodic apnea", "myasthenic syndrome, presynaptic, congenital, associated with episodic apnea", "Myasthenic syndrome, presynaptic, congenital, associated with episodic apnea", "MYASTHENIC SYNDROME, PRESYNAPTIC, CONGENITAL, ASSOCIATED WITH EPISODIC APNEA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myasthenic syndrome 6", "shortest_name_length": 3}
{"curie": "UMLS:C3272487", "names": ["MALT Lymphoma of the Dura", "Dural Extranodal Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dural Extranodal Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue", "shortest_name_length": 25}
{"curie": "MONDO:0014685", "names": ["EPM9", "EMP9", "PME type 9", "progressive myoclonus epilepsy 9", "EPILEPSY, PROGRESSIVE MYOCLONIC, 9", "epilepsy, progressive myoclonic, 9", "LMNB2 progressive myoclonic epilepsy", "progressive myoclonic epilepsy type 9", "Progressive myoclonus epilepsy type 9", "Progressive myoclonic epilepsy type 9", "progressive myoclonus epilepsy type 9", "epilepsy, progressive myoclonic, type 9", "Progressive myoclonic epilepsy type 9 (disorder)", "PME type 9 - progressive myoclonic epilepsy type 9", "progressive myoclonic epilepsy due to LMNB2 deficiency", "Progressive myoclonic epilepsy due to LMNB2 deficiency", "progressive myoclonic epilepsy caused by mutation in LMNB2", "Progressive myoclonic epilepsy due to LMNB2 (lamin B2) deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive myoclonic epilepsy type 9", "shortest_name_length": 4}
{"curie": "UMLS:C4527414", "names": ["Prostate Cancer by Gene Expression Profile", "Prostate Carcinoma by Gene Expression Profile"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Carcinoma by Gene Expression Profile", "shortest_name_length": 42}
{"curie": "MONDO:0014422", "names": ["VUR8", "VESICOURETERAL REFLUX 8", "vesicoureteral reflux 8", "vesicoureteral reflux type 8", "TNXB vesicoureteral reflux (disease)", "vesicoureteral reflux (disease) caused by mutation in TNXB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vesicoureteral reflux 8", "shortest_name_length": 4}
{"curie": "MONDO:0100135", "names": ["DS", "SME", "DEE6", "SMEI", "DRVT", "DEE6A", "EIEE6", "DRAVET SYNDROME", "Dravet syndrome", "Dravet Syndrome", "Dravet Syndromes", "Dravet syndrome NOS", "Dravet syndrome (diagnosis)", "Severe Infantile Myoclonic Epilepsy", "Infantile Severe Myoclonic Epilepsy", "Myoclonic Epilepsy, Severe Infantile", "SEVERE MYOCLONIC EPILEPSY OF INFANCY", "Severe Myoclonic Epilepsy, Infantile", "Severe myoclonic epilepsy of infancy", "Severe Myoclonic Epilepsy of Infancy", "Severe myoclonic epilepsy in infancy", "Severe myoclonus epilepsy of infancy", "Severe Myoclonic Epilepsy Of Infancy", "severe myoclonic epilepsy of infancy", "Myoclonic Epilepsy, Infantile, Severe", "Epilepsy, Myoclonic, Infantile, Severe", "Myoclonic Epilepsy, Severe, Of Infancy", "myoclonic epilepsy, severe, of infancy", "Early Infantile Epileptic Encephalopathy 6", "early infantile epileptic encephalopathy 6", "Severe myoclonic epilepsy in infancy (SMEI)", "developmental and epileptic encephalopathy 6", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 6", "Developmental and Epileptic Encephalopathy 6A", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 6A", "developmental and epileptic encephalopathy 6A", "Severe myoclonic epilepsy in infancy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dravet syndrome", "shortest_name_length": 2}
{"curie": "MONDO:0002124", "names": ["Secondary lacrimal atrophy", "secondary lacrimal atrophy", "lacrimal atrophy secondary", "Secondary lacrimal gland atrophy", "secondary atrophy of lacrimal gland", "Secondary atrophy of lacrimal gland", "Secondary lacrimal atrophy (disorder)", "consecutive atrophy of lacrimal gland", "Consecutive atrophy of lacrimal gland", "secondary lacrimal atrophy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary lacrimal atrophy", "shortest_name_length": 26}
{"curie": "UMLS:C1504441", "names": ["Instillation site itching", "Instillation site pruritus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Instillation site pruritus", "shortest_name_length": 25}
{"curie": "MONDO:0012323", "names": ["LAEB", "EBLA", "Lethal acantholytic erosive disorder", "LETHAL ACANTHOLYTIC EPIDERMOLYSIS BULLOSA", "lethal acantholytic epidermolysis bullosa", "Lethal acantholytic epidermolysis bullosa", "EPIDERMOLYSIS BULLOSA, LETHAL ACANTHOLYTIC", "epidermolysis bullosa, lethal acantholytic", "Epidermolysis bullosa, lethal acantholytic", "Lethal acantholytic erosive disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal acantholytic epidermolysis bullosa", "shortest_name_length": 4}
{"curie": "MONDO:0009216", "names": ["FBS", "GSD type XI", "GSD type 11", "GLUT2 deficiency", "Fanconi-Bickel disease", "FANCONI-BICKEL SYNDROME", "Fanconi-Bickel syndrome", "fanconi bickel syndrome", "Lignac Fanconi Syndrome", "Lignac-Fanconi Syndrome", "Fanconi-Bickel Syndrome", "fanconi-bickel syndrome", "Fanconi Bickel Syndrome", "Fanconi Bickel syndrome", "Lignac-Fanconi syndrome", "Syndrome, Fanconi-Bickel", "Syndrome, Fanconi Bickel", "Bickel Syndrome, Fanconi", "Syndrome, Lignac-Fanconi", "Pseudo-Phlorizin Diabete", "Fanconi-Bickel Syndromes", "Pseudo-phlorizin diabetes", "Diabete, Pseudo-Phlorizin", "Fanconi Type Glycogenosis", "Syndromes, Fanconi-Bickel", "Pseudo Phlorizin Diabetes", "pseudo-phlorizin diabetes", "Pseudo-Phlorizin Diabetes", "PSEUDO-PHLORIZIN DIABETES", "Diabetes, Pseudo-Phlorizin", "glycogenosis Fanconi EXACT", "GLYCOGENOSIS, FANCONI TYPE", "glycogenosis, Fanconi type", "Glycogenosis, Fanconi Type", "glycogen storage disease 11", "Glycogen Storage Disease XI", "GSD due to GLUT2 deficiency", "GLYCOGEN STORAGE DISEASE XI", "Bickel-Fanconi glycogenosis", "glycogen storage disease XI", "Renal glucose-losing syndrome", "glycogen storage disease type 11", "glycogen storage disease type XI", "Glycogen Storage Disease Type XI", "glycogenosis due to GLUT2 deficiency", "Glycogenosis due to GLUT2 deficiency", "Glycogenosis with glucoaminophosphaturia", "hepatic glycogenosis with Fanconi nephropathy", "HEPATIC GLYCOGENOSIS WITH FANCONI NEPHROPATHY", "Hepatic Glycogenosis with Fanconi Nephropathy", "glycogen storage disease due to GLUT2 deficiency", "Glycogen storage disease due to GLUT2 deficiency", "Glycogen Storage Disease Due to GLUT2 Deficiency", "Glycogenosis with glucoaminophosphaturia (disorder)", "hepatorenal glycogenosis with renal fanconi syndrome", "Hepatorenal Glycogenosis with Renal Fanconi Syndrome", "HEPATORENAL GLYCOGENOSIS WITH RENAL FANCONI SYNDROME", "hepatorenal glycogenosis with renal Fanconi syndrome", "Hepatic Glycogenosis with Amino Aciduria and Glucosuria", "hepatic glycogenosis with amino aciduria and glucosuria", "HEPATIC GLYCOGENOSIS WITH AMINO ACIDURIA AND GLUCOSURIA", "Fanconi syndrome with intestinal malabsorption and galactose intolerance", "Fanconi Syndrome with Intestinal Malabsorption and Galactose Intolerance", "FANCONI SYNDROME WITH INTESTINAL MALABSORPTION AND GALACTOSE INTOLERANCE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease due to GLUT2 deficiency", "shortest_name_length": 3}
{"curie": "UMLS:C0033626", "names": ["protein deficiency", "Protein Deficiency", "Protein deficiency", "deficiency protein", "protein; deficiency", "Deficiency, Protein", "deficiency; protein", "Protein Deficiencies", "protein deficiencies", "deficiencies protein", "Deficiencies, Protein"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Protein Deficiency", "shortest_name_length": 18}
{"curie": "MONDO:0013084", "names": ["NBLST4", "NEUROBLASTOMA, SUSCEPTIBILITY TO, 4", "neuroblastoma, susceptibility to, 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuroblastoma, susceptibility to, 4", "shortest_name_length": 6}
{"curie": "UMLS:C1291316", "names": ["Reductase Deficiency", "reductase deficiency", "Deficiency of reductase", "deficiency of reductase", "Deficiency of reductase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Deficiency of reductase", "shortest_name_length": 20}
{"curie": "MONDO:0800130", "names": ["AISIMD", "autoinflammatory syndrome with immunodeficiency", "AUTOINFLAMMATORY SYNDROME, FAMILIAL, WITH OR WITHOUT IMMUNODEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoinflammatory syndrome with immunodeficiency", "shortest_name_length": 6}
{"curie": "MONDO:0030482", "names": ["SPG84", "hereditary spastic paraplegia 84", "spastic paraplegia 84 autosomal recessive", "SPASTIC PARAPLEGIA 84, AUTOSOMAL RECESSIVE", "spastic paraplegia 84, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic paraplegia 84, autosomal recessive", "shortest_name_length": 5}
{"curie": "UMLS:C0242875", "names": ["Ventricular septal rupture", "Ventricular Septal Rupture", "Ventricular Septal Ruptures", "Septal Rupture, Ventricular", "Septal Ruptures, Ventricular", "Interventricular septal rupture", "Interventricular septum rupture", "Rupture of interventricular septum", "Rupture of interventricular septum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ventricular Septal Rupture", "shortest_name_length": 26}
{"curie": "MONDO:0002501", "names": ["brain glioblastoma", "Brain Glioblastoma", "brain Glioblastoma", "brain glioblastoma (disease)", "Brain Glioblastoma Multiforme", "brain glioblastoma multiforme", "grade IV astrocytoma of brain", "grade IV brain astrocytic tumor", "glioblastoma (disease) of brain", "Glioblastoma multiforme of brain", "glioblastoma multiforme of brain", "Glioblastoma Multiforme of Brain", "grade IV astrocytic tumor of brain", "grade IV brain astrocytic neoplasm", "Glioblastoma Multiforme of the Brain", "glioblastoma multiforme of the brain", "grade IV astrocytic neoplasm of brain", "grade IV astrocytic tumor of the brain", "brain glioblastoma multiforme (disease)", "grade IV astrocytic neoplasm of the brain", "Glioblastoma multiforme of brain (disorder)", "glioblastoma multiforme of brain (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brain glioblastoma", "shortest_name_length": 18}
{"curie": "MONDO:0013739", "names": ["CHBL2", "chilblain lupus 2", "CHILBLAIN LUPUS 2", "SAMHD1 chilblain lupus", "Chilblain lupus type 2", "chilblain lupus caused by mutation in SAMHD1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chilblain lupus 2", "shortest_name_length": 5}
{"curie": "MONDO:0042964", "names": ["Azorean disease, type IV", "azorean disease, type iv", "Machado-Joseph disease type 4", "Azorean disease, type IV (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Machado-Joseph disease type 4", "shortest_name_length": 24}
{"curie": "MONDO:0019370", "names": ["Vulvovaginal gingival syndrome", "vulvovaginal gingival syndrome", "Vulvovaginal gingival syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvovaginal gingival syndrome", "shortest_name_length": 30}
{"curie": "MONDO:0015672", "names": ["diprosopus", "Diprosopia", "Diprosopus", "Diprosopus, NOS", "Diprosopus (disorder)", "Monocephalus diprosopus", "Craniofacial duplication", "craniofacial duplication", "Monocephalus diprosopus twins", "Duplication, facial diprosopus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diprosopus", "shortest_name_length": 10}
{"curie": "UMLS:C3272813", "names": ["Colon Cribriform Comedo-Type Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colon Cribriform Comedo-Type Adenocarcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0007015", "names": ["Viral Meningitis", "Meningitis viral", "MENINGITIS VIRAL", "viral meningitis", "Viral meningitis", "meningitis viral", "virus; meningitis", "Meningitis, viral", "meningitis; viral", "Meningitis, Viral", "Viral Meningitides", "meningitis - viral", "Meningitides, Viral", "Meningitis viral NOS", "Viral meningitis NOS", "Abacterial meningitis", "abacterial; meningitis", "meningitis; abacterial", "aseptic viral meningitis", "aseptic meningitis viral", "Aseptic meningitis, viral", "Viral meningitis (disorder)", "Unspecified viral meningitis", "viral meningitis (diagnosis)", "Viral meningitis, unspecified", "infection; viral, central nervous system, meningitis", "viral; infection, central nervous system, meningitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "viral meningitis", "shortest_name_length": 16}
{"curie": "MONDO:0044330", "names": ["HKPX4", "HYPEREKPLEXIA 4", "hyperekplexia 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperekplexia 4", "shortest_name_length": 5}
{"curie": "MONDO:0020761", "names": ["BOWEN DISEASE", "bowen disease", "Bowen disease", "Bowen Disease", "Disease;Bowens", "Bowens Disease", "Bowens disease", "Disease, Bowen", "bowens disease", "disease bowen's", "Bowen's Disease", "Bowen's disease", "BOWEN'S DISEASE", "bowen's disease", "Disease, Bowen's", "BD - Bowen's disease", "Bowen's disease of skin", "Bowen Disease of the Skin", "Bowen disease of the skin", "Bowen's disease of the skin", "Bowen's Disease of the Skin", "Bowen's disease (diagnosis)", "Bowen's disease (morphologic abnormality)", "Intraepidermal squamous cell carcinoma, Bowen type", "Intraepidermal Squamous Cell Carcinoma, Bowen Type", "intraepidermal squamous cell carcinoma, Bowen type", "Intraepidermal squamous cell carcinoma, Bowen's type", "SCC - Intraepidermal squamous cell carcinoma - Bowen's type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bowen disease of the skin", "shortest_name_length": 13}
{"curie": "MONDO:0011813", "names": ["Papa3", "PAPA3", "postaxial polydactyly, type A3", "POSTAXIAL POLYDACTYLY, TYPE A3", "Postaxial Polydactyly, Type A3", "polydactyly, postaxial, type A3", "POLYDACTYLY, POSTAXIAL, TYPE A3", "Polydactyly, Postaxial, Type A3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polydactyly, postaxial, type A3", "shortest_name_length": 5}
{"curie": "UMLS:C4087213", "names": ["Vascular access site bleeding", "Vascular access site hemorrhage", "Vascular access site haemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vascular access site hemorrhage", "shortest_name_length": 29}
{"curie": "MONDO:0002724", "names": ["mastocytoma", "Mast Cell Tumor", "tumor mast cell", "mast cell tumor", "Mast cell tumor", "tumor; mast cell", "MAST CELL TUMORS", "mast cell tumors", "mast cell; tumor", "Mast Cell Tumors", "Mast cell tumour", "mast cell neoplasm", "Mast Cell Neoplasm", "Mast cell neoplasm", "tumor of Mast cells", "Tumor of Mast Cells", "Mast cell tumor NOS", "Mast cell tumor, NOS", "neoplasm of mast cell", "Mast cell tumour, NOS", "neoplasm of Mast cells", "Neoplasm of Mast Cells", "tumor of the Mast cells", "Tumor of the Mast Cells", "neoplasm of the Mast cells", "Neoplasm of the Mast Cells", "Mast cell neoplasm (disorder)", "Mast cell neoplasm (diagnosis)", "Mast cell neoplasm (morphology)", "Mast cell Proliferative disease", "Mast Cell Proliferative Disease", "Mast cell proliferative disease", "Mast cell neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mast cell neoplasm", "shortest_name_length": 11}
{"curie": "UMLS:C0266924", "names": ["Chronic pericoronitis", "chronic pericoronitis", "Chronic Pericoronitis", "Chronic pericoronitis (disorder)", "chronic pericoronitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic pericoronitis", "shortest_name_length": 21}
{"curie": "MONDO:0006665", "names": ["Gastric atrophy", "Gastric Atrophy", "gastric atrophy", "atrophy gastric", "atrophy; gastric", "Atrophic Gastritis", "gastritis atrophic", "Gastritis atrophic", "GASTRITIS ATROPHIC", "Gastritis;atrophic", "atrophic gastritis", "Atrophic gastritis", "ATROPHIC GASTRITIS", "Gastritis, Atrophic", "atrophic; gastritis", "gastritis; atrophic", "autoimmune gastritis", "Autoimmune gastritis", "Atrophic Gastritides", "Autoimmune Gastritis", "atrophic Gastritides", "Gastritides, Atrophic", "Gastritides, atrophic", "AG - Atrophic gastritis", "Chronic atrophic gastritis", "Chronic Atrophic Gastritis", "chronic atrophic gastritis", "gastritis; chronic, atrophic", "chronic; gastritis, atrophic", "Atrophic gastritis (disorder)", "CAG - Chronic atrophic gastritis", "chronic atrophic gastritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic atrophic gastritis", "shortest_name_length": 15}
{"curie": "MONDO:0002052", "names": ["adenitis", "Adenitis", "LYMPHADENITIS", "lymphadenitis", "Lymphadenitis", "Acute adenitis", "acute adenitis", "lymph nodeitis", "Lymphadenitides", "acute; adenitis", "adenitis; acute", "Chronic adenitis", "chronic adenitis", "chronic; adenitis", "adenitis; chronic", "Lymphadenitis NOS", "Lymphadenitis, NOS", "Lymph node inflamed", "Lymphadenitis acute", "Lymphadenitis;acute", "Acute lymphadenitis", "acute lymphadenitis", "Acute Lymphadenitis", "lymphadenitis; acute", "acute; lymphadenitis", "Chronic lymphadenitis", "lymphadenitis chronic", "gland infection lymph", "Chronic Lymphadenitis", "Lymph gland infection", "Lymphadenitis chronic", "lymph gland infection", "Lymphadenitis;chronic", "Chronic adenitis, NOS", "chronic Lymphadenitis", "chronic lymphadenitis", "Infection;lymph glands", "lymph glands infection", "chronic; lymphadenitis", "glands infection lymph", "infection; lymph gland", "lymph gland; infection", "lymphadenitis; chronic", "lymphadenitis (disease)", "Lymph node inflammation", "lymph node inflammation", "glands infections lymph", "Lymphadenitis (disorder)", "inflammation; lymph node", "lymph node; inflammation", "lymphadenitis (diagnosis)", "Inflammation of lymph node", "inflammation of lymph node", "Chronic lymphadenitis, NOS", "Acute lymphadenitis (disorder)", "Inflammation of the lymph nodes", "acute lymphadenitis (diagnosis)", "Acute lymphadenitis, unspecified", "Chronic lymphadenitis (disorder)", "Chronic adenitis any lymph node, except mesenteric", "Chronic lymphadenitis any lymph node, except mesenteric"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphadenitis", "shortest_name_length": 8}
{"curie": "UMLS:C2350873", "names": ["Beryllium Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Beryllium Disease", "shortest_name_length": 17}
{"curie": "MONDO:0019654", "names": ["familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis", "shortest_name_length": 89}
{"curie": "UMLS:C1332218", "names": ["Ovarian Granulosa Cell Tumor", "Adult Ovarian Granulosa Cell Tumor", "Adult Type Ovarian Granulosa Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Type Ovarian Granulosa Cell Tumor", "shortest_name_length": 28}
{"curie": "MONDO:0002399", "names": ["benign synovioma", "Synovioma, benign", "Nodular Tenosynovitis", "Nodular tenosynovitis", "nodular tenosynovitis", "Tenosynovitis, nodular", "Tenosynovitis, Nodular", "Nodular Tenosynovitides", "benign tumor of synovium", "benign tumor of Synovium", "Tenosynovitides, Nodular", "cell giant sheath tendon tumor", "giant cell tumor tendon sheath", "giant cell tendon sheath tumor", "giant cell tumour tendon sheath", "Localized Nodular Tenosynovitis", "cell giant sheath tendon tumour", "Nodular Tenosynovitis, Localized", "Tenosynovitis, Localized Nodular", "Nodular tenosynovitis (disorder)", "Localized Nodular Tenosynovitides", "Nodular Tenosynovitides, Localized", "Tenosynovitides, Localized Nodular", "Localized Tenosynovial Giant Cell Tumor", "localized tenosynovial giant cell tumor", "Tenosynovial giant cell tumor, localized", "Tenosynovial giant cell tumour, localised", "localized Giant cell tumor of Tenosynovium", "Localized Pigmented Villonodular Synovitis", "Localized Giant Cell Tumor of Tenosynovium", "localized giant cell tumor of Tenosynovium", "localized tenosynovial giant cell neoplasm", "Localized Tenosynovial Giant Cell Neoplasm", "localized giant cell tumor of tendon sheath", "Localized Giant Cell Tumor of Tendon Sheath", "synovioma, benign (morphologic abnormality)", "Localized Giant Cell Neoplasm of Tenosynovium", "Tenosynovial Giant Cell Tumor, Localized Type", "localized giant cell neoplasm of Tenosynovium", "tenosynovial giant cell tumor, localized type", "Localized Giant Cell Tumor of the Tenosynovium", "localized giant cell neoplasm of tendon sheath", "Localized Giant Cell Neoplasm of Tendon Sheath", "localized giant cell tumor of the Tenosynovium", "Localized Giant Cell Tumor of the Tendon Sheath", "localized giant cell neoplasm of the Tenosynovium", "Localized Giant Cell Neoplasm of the Tenosynovium", "Tenosynovial giant cell tumor, localized (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tenosynovial giant cell tumor, localized type", "shortest_name_length": 16}
{"curie": "MONDO:0100252", "names": ["HFTC", "HFTC1", "Morbus Teutschlaender", "Teutschlaender disease, familial", "hyperostosis-hyperphosphatemia syndrome", "calcinosis, tumoral, with hyperphosphatemia", "tumoral calcinosis, primary Hyperphosphatemic", "tumoral calcinosis, hyperphosphatemic, familial", "tumoral calcinosis, HYPERPHOSPHATEMIC, familial, 1", "TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 1", "tumoral calcinosis, Hyperphosphatemic, familial, 1", "tumoral calcinosis, hyperphosphatemic, familial, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tumoral calcinosis, hyperphosphatemic, familial, 1", "shortest_name_length": 4}
{"curie": "MONDO:0006510", "names": ["renal absorption disease", "disorder of renal absorption", "renal tubular transport errors", "Renal Tubular Transport Errors", "renal tubular transport disease", "renal tubular transport, inborn error", "Renal Tubular Transport, Inborn Error", "Renal Tubular Transport, Inborn Errors", "Kidney Tubular Transport, Inborn Error", "kidney tubular transport, inborn error", "kidney tubular transport, inborn errors", "Kidney Tubular Transport, Inborn Errors", "inborn renal tubular transport disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal tubular transport disease", "shortest_name_length": 24}
{"curie": "MONDO:0004057", "names": ["micropapillary urothelial carcinoma", "Micropapillary Urothelial Carcinoma", "micropapillary variant infiltrating bladder urothelial carcinoma", "Infiltrating Bladder Urothelial Carcinoma, Micropapillary Variant", "infiltrating bladder urothelial carcinoma, micropapillary variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "micropapillary variant infiltrating bladder urothelial carcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C4520965", "names": ["Stage II Pancreatic Cancer", "Pancreatic Cancer Stage II", "stage II pancreatic cancer", "Stage II Pancreatic Carcinoma", "Stage II Carcinoma of Pancreas", "Stage II Carcinoma of the Pancreas", "Stage II Pancreatic Cancer AJCC v6", "Stage II Pancreatic Cancer AJCC v7", "Stage II Pancreatic Cancer AJCC v6 and v7", "Stage II Exocrine and Endocrine Pancreatic Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Pancreatic Cancer AJCC v6 and v7", "shortest_name_length": 26}
{"curie": "MONDO:0006540", "names": ["Dysidria", "Pompholyx", "pompholyx", "Dyshidria", "POMPHOLYX", "Dysidrosis", "dishydrosis", "Dyshidrosis", "DYSHYDROSIS", "dyshydrosis", "dyshidrosis", "DISHYDROSIS", "DYSHIDROSIS", "cheiropompholyx", "Cheiropompholyx", "pompholyx eczema", "Pompholyx eczema", "Dyshydrotic Eczema", "Dyshidrotic Eczema", "DYSHIDROTIC ECZEMA", "DYSHYDROTIC eczema", "ECZEMA DYSHIDROTIC", "Dyshidrotic eczema", "dyshidrotic eczema", "eczema dyshidrotic", "DYSHYDROTIC ECZEMA", "Eczema;dyshidrotic", "dyshydrotic eczema", "Eczema, Dyshydrotic", "Dyshidrotic Eczemas", "Eczema, Dyshidrotic", "Dyshydrotic Eczemas", "Cheiropodopompholyx", "eczema; dyshydrotic", "dyshydrotic; eczema", "Eczemas, Dyshydrotic", "Eczemas, Dyshidrotic", "dyshidrotic dermatitis", "Dyshidrotic dermatitis", "dyshidrosis (diagnosis)", "dyshidrotic hand eczema", "Disgidroticheskaya eczema", "Dyshidrotic dermatitis, NOS", "Vesicular Palmoplantar Eczema", "eczema dyshidrotic (diagnosis)", "Palmoplantar Eczema, Vesicular", "Eczema, Vesicular Palmoplantar", "Vesicular Palmoplantar Eczemas", "Eczemas, Vesicular Palmoplantar", "Palmoplantar Eczemas, Vesicular", "Vesicular eczema of hands and feet", "vesicular eczema of hands and/or feet", "Vesicular eczema of hands and/or feet", "Vesicular eruption of palms and soles"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyshidrosis", "shortest_name_length": 8}
{"curie": "MONDO:0009199", "names": ["ethanolaminuria", "Ethanolaminosis", "ethanolaminosis", "Ethanolaminuria", "ETHANOLAMINOSIS", "Ethanolaminosis (disorder)", "ethanolaminuria (diagnosis)", "ETHANOLAMINE KINASE DEFICIENCY", "ethanolamine kinase deficiency", "Ethanolamine kinase deficiency", "Ethanolamine Kinase Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ethanolaminosis", "shortest_name_length": 15}
{"curie": "MONDO:0007886", "names": ["UL", "fibroids", "FIBROIDS", "Fibroids", "Leiomyoma", "leiomyoma", "Myofibroma", "Fibromyoma", "myofibroma", "leiomyomas", "fibromyoma", "Myoma;uterus", "uterus myoma", "Uterine Myoma", "uterine myoma", "UTERUS, MYOMA", "Uterine myoma", "Fibroid uterus", "Leiomyofibroma", "uterus fibroma", "Fibroid Uterus", "uterus fibroid", "UTERUS FIBROMA", "fibroid uterus", "leiomyofibroma", "Fibroleiomyoma", "fibroleiomyoma", "Fibroid;uterus", "uterus fibroids", "UTERINE FIBROMA", "uterine fibroid", "uterine fibroma", "Uterus, Fibroid", "Uterine fibroma", "UTERINE FIBROID", "Uterine fibroid", "Uterine Fibroma", "Uterine Fibroid", "Uterine fibroids", "Fibroid, Uterine", "Uterine Fibroids", "uterine fibromas", "uterus leiomyoma", "uterine fibroids", "Uterine Fibromas", "UTERUS, FIBROIDS", "Fibroma, Uterine", "Uterine leiomyoma", "Fibroids, Uterine", "Fibromyoma;uterus", "leiomyoma; uterus", "UTERINE LEIOMYOMA", "UTERUS, LEIOMYOMA", "uterine leiomyoma", "Fibromas, Uterine", "Uterine Leiomyoma", "Fibromyoma uterus", "uterus; leiomyoma", "leiomyoma, uterine", "UTERUS, FIBROMYOMA", "Uterine leiomyomas", "uterine fibromyoma", "UTERINE FIBROMYOMA", "uterus; fibromyoma", "LEIOMYOMA, UTERINE", "Uterine fibromyoma", "fibromyoma; uterus", "Leiomyoma, Uterine", "plexiform leiomyoma", "uterine leiomyomata", "Uterine Leiomyomata", "Uterine leiomyomata", "leiomyoma of uterus", "Plexiform leiomyoma", "Leiomyoma of uterus", "uterine body fibroid", "Leiomyoma (disorder)", "Corpus Uteri Fibroid", "Uterine Body Fibroid", "corpus uteri fibroid", "uterine leiomyoma nos", "Uterine Body Leiomyoma", "uterine body leiomyoma", "uterine corpus fibroid", "Uterine Corpus Fibroid", "corpus uteri leiomyoma", "Uterine leiomyoma, NOS", "Corpus Uteri Leiomyoma", "Body of Uterus Fibroid", "body of uterus fibroid", "fibroid of uterine body", "fibroid of corpus uteri", "Fibroid of Corpus Uteri", "Fibroid of Uterine Body", "tumor of uterine muscle", "Uterine Corpus Leiomyoma", "uterine corpus leiomyoma", "fibromyoma of the uterus", "Body of Uterus Leiomyoma", "body of uterus leiomyoma", "Fibroid of Body of Uterus", "leiomyoma of Corpus Uteri", "Fibroid of Uterine Corpus", "leiomyoma of corpus uteri", "fibroid of uterine corpus", "fibroid of body of uterus", "Leiomyoma of Uterine Body", "Benign uterine leiomyomas", "Leiomyoma of Corpus Uteri", "leiomyoma of uterine body", "benign leiomyoma of uterus", "Uterine leiomyomas, benign", "Uterine Corpus Leiomyomata", "uterine corpus leiomyomata", "Leiomyoma of body of uterus", "leiomyoma of body of uterus", "fibroid of the uterine body", "fibroid of the corpus uteri", "Leiomyoma of Body of Uterus", "Fibroid of the Uterine Body", "Fibroid of the Corpus Uteri", "leiomyoma of uterine corpus", "Leiomyoma of Uterine Corpus", "Uterine leiomyoma - fibroids", "Uterine leiomyoma (disorder)", "fibroid of the uterine corpus", "fibroid of the body of uterus", "leiomyoma of the corpus uteri", "leiomyoma of the uterine body", "Fibroid of the Body of Uterus", "Fibroid of the Uterine Corpus", "Leiomyoma of the Corpus Uteri", "Leiomyoma of the Uterine Body", "Leiomyoma of the Uterine Corpus", "leiomyoma of the uterine corpus", "leiomyoma of the body of uterus", "Leiomyoma of the Body of Uterus", "Leiomyoma of uterus, unspecified", "benign leiomyoma of uterus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine corpus leiomyoma", "shortest_name_length": 2}
{"curie": "UMLS:C5418771", "names": ["Recurrent Ovarian Undifferentiated Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Ovarian Undifferentiated Carcinoma", "shortest_name_length": 44}
{"curie": "UMLS:C0149697", "names": ["Foot injury", "wound; foot", "foot; wound", "foot injury", "injury foot", "FOOT INJURY", "Foot Injury", "Injury, Foot", "foot; injury", "injury; foot", "Foot Injuries", "foot injuries", "wound of foot", "injuries foot", "of foot injury", "injury of foot", "Injury of foot", "Injuries, Foot", "foot/feet injury", "Injury;foot/feet", "FOOT INJURY WOUND NOS", "disorders foot injuries", "Injury of foot (disorder)", "Foot--Wounds and injuries", "injury of foot (diagnosis)", "wound of foot (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Foot Injuries", "shortest_name_length": 11}
{"curie": "UMLS:C4053902", "names": ["Ulcerative Colitis Flare"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ulcerative Colitis Flare", "shortest_name_length": 24}
{"curie": "MONDO:0013273", "names": ["Trisomy 16pter", "Dup(16)(p13.3)", "dup(16)(p13.3)", "trisomy 16pter", "Distal trisomy 16p", "distal trisomy 16p", "16p13.3 duplication", "Distal duplication 16p", "distal duplication 16p", "Telomeric duplication 16p", "telomeric duplication 16p", "chromosome 16p13.3 duplication", "interstitial 16p13.3 duplication", "16p13.3 microduplication syndrome", "chromosome 16p13.3 duplication syndrome", "CHROMOSOME 16p13.3 DUPLICATION SYNDROME", "16p13.3 microduplication syndrome (disorder)", "chromosome 16p13.3 duplication syndrome, isolated cases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 16p13.3 duplication syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0018177", "names": ["GBM", "Glioblastoma", "glioblastoma", "glioblastomas", "Glioblastomas", "Glioblastoma NOS", "Glioblastoma, NOS", "GBM (Glioblastoma)", "GBM (glioblastoma)", "WHO grade IV glioma", "grade iv astrocytoma", "Grade IV Astrocytoma", "grade IV astrocytoma", "Astrocytoma, Grade IV", "Grade IV Astrocytomas", "glioblastoma (disease)", "Astrocytomas, Grade IV", "Malignant glioblastoma", "GLIOBLASTOMA MULTIFORME", "glioblastoma multiforme", "ASTROCYTOMA, GRADES 3-4", "CNS, glioblastoma (GBM)", "Glioblastoma Multiforme", "Glioblastoma multiforme", "grade IV astrocytic tumor", "Spongioblastoma multiforme", "Spongioblastoma Multiforme", "spongioblastoma multiforme", "SPONGIOBLASTOMA MULTIFORME", "grade IV astrocytic neoplasm", "GBM - glioblastoma multiforme", "adult glioblastoma multiforme", "GLM - Glioblastoma multiforme", "glioblastoma multiforme (GBM)", "GBM - Glioblastoma multiforme", "GLM - glioblastoma multiforme", "glioblastoma; unspecified site", "glioma glioblastoma multiforme", "primary glioblastoma multiforme", "grade IV adult Astrocytic tumor", "grade IV adult astrocytic tumor", "CANCER, GLIOBLASTOMA MULTIFORME", "gliosarcoma (histologic variant)", "glioblastoma multiforme (disease)", "Glioblastoma multiforme (disorder)", "glioblastoma multiforme (diagnosis)", "BRAIN TUMOR, GLIOBLASTOMA MULTIFORME", "Glioblastoma, Not Otherwise Specified", "Glioblastoma (morphologic abnormality)", "giant cell glioblastoma (histologic variant)", "INTRACRANIAL NEOPLASM, GLIOBLASTOMA MULTIFORME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glioblastoma", "shortest_name_length": 3}
{"curie": "MONDO:0010742", "names": ["Tas", "TAS", "THAS", "Cantrell syndrome", "cantrell pentalogy", "pentalogy cantrell", "Cantrell deformity", "Cantrell Pentalogy", "Cantrell pentalogy", "Cantrells Pentalogy", "Pentalogy, Cantrell", "cantrell's syndrome", "Cantrell's Pentalogy", "pentalogy of cantrell", "PENTALOGY OF CANTRELL", "Pentalogy, Cantrell's", "Pentalogy of Cantrell", "pentalogy of Cantrell", "Midline Defects, X-Linked", "THORACOABDOMINAL SYNDROME", "Thoracoabdominal Syndrome", "thoracoabdominal syndrome", "MIDLINE DEFECTS, X-LINKED", "Midline defects, X-linked", "Thoraco-abdominal syndrome", "thoraco-abdominal syndrome", "Thoracoabdominal Syndromes", "Pentalogy of Cantrell (disorder)", "Cantrell Haller Ravitch syndrome", "Cantrell Haller Ravitsch syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pentalogy of Cantrell", "shortest_name_length": 3}
{"curie": "MONDO:0007754", "names": ["HYPRPP", "Palmoplantar hyperhidrosis", "hyperhidrosis, primary palmar", "HYPERHIDROSIS, PRIMARY PALMAR", "Hyperhidrosis (palms and soles)", "Hyperhidrosis of palms and soles", "HYPERHIDROSIS PALMARIS ET PLANTARIS", "Hyperhidrosis Palmaris Et Plantaris", "hyperhidrosis palmaris ET plantaris", "Palmoplantar hyperhidrosis (disorder)", "Excessive sweating of palms and soles"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperhidrosis palmaris ET plantaris", "shortest_name_length": 6}
{"curie": "UMLS:C1142012", "names": ["Infusion site abscess"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infusion site abscess", "shortest_name_length": 21}
{"curie": "MONDO:0001982", "names": ["Pick-Niemann", "Niemann-Pick", "Neuronal lipidosis", "Niemann-Pick Disease", "neimann pick disease", "lipoid histiocytosis", "Niemann-Pick disease", "niemann pick disease", "disease niemann-pick", "HISTIOCYTOSIS, LIPID", "niemann-pick disease", "NIEMANN-PICK DISEASE", "neimann-pick disease", "Niemann Pick Disease", "Niemann Pick disease", "niemann-pick diseases", "Niemann-Pick Diseases", "disease neimann picks", "Niemann-Pick diseases", "disease niemann picks", "Niemann Pick Diseases", "sphingomyelin lipidosis", "Sphingomyelin lipidosis", "SPHINGOMYELIN LIPIDOSIS", "LIPIDOSIS, SPHINGOMYELIN", "Niemann-Pick disease, NOS", "Sphingomyelinase deficiency", "sphingomyelinase deficiency", "type A Niemann-Pick disease", "Sphingomyelin lipidosis, NOS", "Neuronal cholesterol lipidosis", "Niemann-Pick disease (diagnosis)", "Niemann-Pick disease, unspecified", "Sphingomyelin/cholesterol lipidosis", "Sphingomyelin/Cholesterol Lipidosis", "sphingomyelinase deficiency disease", "Neuronal cholesterol lipidosis, NOS", "sphingomyelin/cholesterol lipidosis", "Sphingomyelinase Deficiency Disease", "Sphingomyelin/cholesterol lipidosis, NOS", "Niemann-Pick disease, subacute juvenile form", "lipoid histiocytosis (classical phosphatide)", "Sphingomyelin/cholesterol lipidosis (disorder)", "Niemann-Pick disease with cholesterol esterification block"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Niemann-Pick disease", "shortest_name_length": 12}
{"curie": "UMLS:C4744616", "names": ["Localized Gastroesophageal Junction Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized Gastroesophageal Junction Adenocarcinoma", "shortest_name_length": 50}
{"curie": "UMLS:C5206664", "names": ["Penile Glomus Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Penile Glomus Tumor", "shortest_name_length": 19}
{"curie": "MONDO:0011884", "names": ["HOPP syndrome", "Hopp syndrome", "HOPP SYNDROME", "hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome", "Hypotrichosis-Osteolysis-Periodontitis-Palmoplantar Keratoderma Syndrome", "Hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome", "HYPOTRICHOSIS-OSTEOLYSIS-PERIODONTITIS-PALMOPLANTAR KERATODERMA SYNDROME", "Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome", "hypotrichosis-osteolysis-periodontitis-palmoplantar hyperkeratosis syndrome", "Hypotrichosis-osteolysis-periodontitis-palmoplantar hyperkeratosis syndrome", "Hypotrichosis-striate palmoplantar keratoderma-acroosteolysis-periodontitis syndrome", "hypotrichosis-striate palmoplantar keratoderma-acroosteolysis-periodontitis syndrome", "Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome (disorder)", "Hypotrichosis-striate palmoplantar hyperkeratosis-acroosteolysis-periodontitis syndrome", "hypotrichosis-striate palmoplantar hyperkeratosis-acroosteolysis-periodontitis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome", "shortest_name_length": 13}
{"curie": "UMLS:C3831526", "names": ["Antepartum Obstetric Thromboembolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Antepartum Obstetric Thromboembolism", "shortest_name_length": 36}
{"curie": "UMLS:C2826588", "names": ["Chronic Active Colitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic Active Colitis", "shortest_name_length": 22}
{"curie": "MONDO:0008819", "names": ["ARTERIOSCLEROSIS, SEVERE JUVENILE", "Arteriosclerosis, Severe Juvenile", "arteriosclerosis, severe juvenile"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arteriosclerosis, severe juvenile", "shortest_name_length": 33}
{"curie": "UMLS:C0263111", "names": ["Perineal abscess", "perineal abscess", "Perineal Abscess", "PERINEUM ABSCESS", "Abscess of perineum", "Abscess of perineum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abscess of perineum", "shortest_name_length": 16}
{"curie": "UMLS:C5238238", "names": ["Locally Advanced Genitourinary System Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Genitourinary System Carcinoma", "shortest_name_length": 47}
{"curie": "UMLS:C1336713", "names": ["testicular seminoma and choriocarcinoma", "testicular choriocarcinoma and seminoma", "choriocarcinoma and seminoma, testicular", "seminoma and choriocarcinoma of the testis", "testis cancer, seminoma and choriocarcinoma", "testis cancer, choriocarcinoma and seminoma", "Mixed Choriocarcinoma and Seminoma of Testis", "Testicular Mixed Choriocarcinoma and Seminoma", "testicle cancer, choriocarcinoma and seminoma", "testicular cancer, seminoma and choriocarcinoma", "testicular cancer, choriocarcinoma and seminoma", "Mixed Choriocarcinoma and Seminoma of the Testis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular Mixed Choriocarcinoma and Seminoma", "shortest_name_length": 39}
{"curie": "UMLS:C1306726", "names": ["Congenital nevus", "nevus congenital", "congenital nevus", "Naevus;congenital", "congenital naevus", "Congenital naevus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital nevus", "shortest_name_length": 16}
{"curie": "MONDO:0020210", "names": ["syndromic hyperopia", "syndrome associated with hyperopia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic hyperopia", "shortest_name_length": 19}
{"curie": "UMLS:C0877125", "names": ["Coma acidotic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Coma acidotic", "shortest_name_length": 13}
{"curie": "UMLS:C5206600", "names": ["Paratesticular Rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paratesticular Rhabdomyosarcoma", "shortest_name_length": 31}
{"curie": "MONDO:0018374", "names": ["secondary AVN", "secondary avascular necrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary avascular necrosis", "shortest_name_length": 13}
{"curie": "UMLS:C0409497", "names": ["Joint injury", "injury joint", "joint trauma", "JOINT TRAUMA", "joint injury", "injury; joint", "injury joints", "joint; injury", "injuries joint", "injuries joints", "injury of joint", "Injury;joint(s)", "Joint injury, NOS", "Joint injury (disorder)", "injury of joint (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joint injury", "shortest_name_length": 12}
{"curie": "MONDO:0043783", "names": ["Underwood", "sclerema adiposum", "Sclerema adiposum", "newborn; sclerema", "sclerema; newborn", "sclerema; adiposum", "adiposum; sclerema", "underwood's disease", "Sclerema Neonatorum", "sclerema neonatorum", "Sclerema neonatorum", "Underwood's disease", "sclerema; neonatorum", "neonatorum; sclerema", "Pre-agonal induration", "Sclerema neonatorum (disorder)", "sclerema neonatorum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sclerema neonatorum", "shortest_name_length": 9}
{"curie": "MONDO:0024276", "names": ["Glandular Neoplasm", "Neoplasm, Glandular", "Glandular Neoplasms", "glandular cell tumor", "Neoplasms, Glandular", "Glandular Cell Neoplasm", "glandular cell neoplasm", "Glandular cell neoplasm", "Glandular Cell Neoplasms", "Cell Neoplasm, Glandular", "Neoplasm, Glandular Cell", "glandular cell epithelial neoplasm", "Glandular Cell Epithelium Neoplasm", "glandular cell epithelium neoplasm", "Glandular Cell Epithelial Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glandular cell neoplasm", "shortest_name_length": 18}
{"curie": "MONDO:0008509", "names": ["Sym2", "SYM2", "distal symphalangism", "Distal symphalangism", "Symphalangism, distal", "Symphalangism, Distal", "symphalangism, distal", "SYMPHALANGISM, DISTAL", "distal symphalangism (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal symphalangism", "shortest_name_length": 4}
{"curie": "UMLS:C1706819", "names": ["Anterior Pituitary Gland Neoplasm", "Neoplasm of the Anterior Lobe of the Pituitary Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anterior Pituitary Gland Neoplasm", "shortest_name_length": 33}
{"curie": "UMLS:C0349672", "names": ["Prostate Ductal Adenocarcinoma", "Prostate Endometrioid Carcinoma", "Prostatic Endometrioid Carcinoma", "Ductal Adenocarcinoma of Prostate", "Endometrioid carcinoma of prostate", "Endometrioid Carcinoma of Prostate", "Prostate Endometrioid Adenocarcinoma", "Ductal Adenocarcinoma of the Prostate", "Endometrioid Carcinoma of the Prostate", "Endometrioid Adenocarcinoma of Prostate", "Endometrioid Adenocarcinoma of the Prostate", "Endometrioid carcinoma of prostate (disorder)", "Endometrioid carcinoma of prostate (diagnosis)", "prostate gland malignant carcinoma endometrioid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endometrioid carcinoma of prostate", "shortest_name_length": 30}
{"curie": "MONDO:0007572", "names": ["PFCP", "ECYT1", "familial polycythemia", "Familial polycythemia", "Familial Polycythemia", "polycythemia; familial", "familial; polycythemia", "Familial polycythaemia", "Polycythemia, familial", "familial erythrocytosis", "Familial erythrocytosis", "erythrocytosis, somatic", "Familial Erythrocytosis", "erythrocytosis; familial", "familial; erythrocytosis", "Congenital erythrocytosis", "Congenital Erythrocytosis", "Hereditary Erythrocytosis", "familial erythrocytosis 1", "Erythrocytosis familial, 1", "Familial erythrocytosis, 1", "EPOR familial polycythemia", "familial erythrocytosis, 1", "Erythrocytosis, Familial, 1", "erythrocytosis, familial, 1", "ERYTHROCYTOSIS, FAMILIAL, 1", "Benign Familial Polycythemia", "Erythropoietin polycythaemia", "Familial benign polycythemia", "Benign familial polycythemia", "Primary familial polycythemia", "POLYCYTHEMIA, BENIGN FAMILIAL", "Primary Familial Polycythemia", "primary familial polycythemia", "familial erythrocytosis type 1", "Hereditary pure erythrocytosis", "ECYT1 familial erythrocytosis-1", "erythrocytosis, familial, type 1", "ERYTHROCYTOSIS, PRIMARY FAMILIAL", "Essential hypererythropoietinemia", "familial polycythemia (diagnosis)", "primary congenital erythrocytosis", "Primary congenital erythrocytosis", "Familial erythrocytosis (disorder)", "autosomal dominant benign erythrocytosis", "erythrocytosis autosomal dominant benign", "Erythrocytosis autosomal dominant benign", "erythrocytosis, autosomal dominant benign", "Erythrocytosis, Autosomal Dominant Benign", "ERYTHROCYTOSIS, AUTOSOMAL DOMINANT BENIGN", "Primary familial and congenital polycythemia", "primary familial and congenital polycythemia", "POLYCYTHEMIA, PRIMARY FAMILIAL AND CONGENITAL", "polycythemia, primary familial and congenital", "Polycythemia, primary familial and congenital", "familial polycythemia caused by mutation in EPOR", "primary familial polycythemia due to EPO receptor mutation", "congenital polycythemia due to erythropoietin receptor mutation", "Congenital polycythemia due to erythropoietin receptor mutation", "Congenital erythrocytosis due to erythropoietin receptor mutation", "congenital erythrocytosis due to erythropoietin receptor mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary familial polycythemia due to EPO receptor mutation", "shortest_name_length": 4}
{"curie": "MONDO:0009320", "names": ["Hall-Riggs syndrome", "Hall Riggs syndrome", "Hall Riggs syndrome (disorder)", "Hall Riggs syndrome (diagnosis)", "Hall Riggs mental retardation syndrome", "HALL-Riggs mental retardation syndrome", "HALL-RIGGS MENTAL RETARDATION SYNDROME", "Hall-Riggs Mental Retardation Syndrome", "Hall Riggs intellectual disability syndrome", "HALL-Riggs intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hall-Riggs syndrome", "shortest_name_length": 19}
{"curie": "MONDO:0010499", "names": ["RTSC2", "Ritscher-Schinzel syndrome 2", "RITSCHER-SCHINZEL SYNDROME 2", "Ritscher-Schinzel syndrome type 2", "CCDC22 Ritscher-Schinzel syndrome", "Ritscher-Schinzel syndrome 2, X-linked recessive", "Ritscher-Schinzel syndrome caused by mutation in CCDC22"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ritscher-Schinzel syndrome 2", "shortest_name_length": 5}
{"curie": "UMLS:C0265040", "names": ["External piles", "external piles", "External hemorrhoid", "external hemorrhoid", "HEMORRHOID EXTERNAL", "External Hemorrhoid", "External haemorrhoid", "External hemorrhoids", "external hemorrhoids", "hemorrhoids external", "hemorrhoids; external", "External haemorrhoids", "external; hemorrhoids", "Hemorrhoids, external", "External hemorrhoids, NOS", "External hemorrhoids (disorder)", "external hemorrhoids (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "External hemorrhoids (disorder)", "shortest_name_length": 14}
{"curie": "MONDO:0024554", "names": ["D2HGA", "D2HGA1", "D-2-hydroxyglutaric aciduria", "D-2-HYDROXYGLUTARIC ACIDURIA 1", "D-2-hydroxyglutaric aciduria 1", "D2HGDH D-2-hydroxyglutaric aciduria", "D-2-hydroxyglutaric aciduria caused by mutation in D2HGDH"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "D-2-hydroxyglutaric aciduria 1", "shortest_name_length": 5}
{"curie": "MONDO:0006843", "names": ["macula hole", "macular hole", "Macular hole", "hole macular", "Macular Hole", "hole; macula", "macula; hole", "Hole, Macular", "Macular holes", "macular holes", "Macular Holes", "holes macular", "Holes, Macular", "Macular hole (disorder)", "macular hole (diagnosis)", "macular hole (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macular holes", "shortest_name_length": 11}
{"curie": "MONDO:0012306", "names": ["RCM2", "restrictive cardiomyopathy 2", "familial restrictive cardiomyopathy 2", "CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 2", "Cardiomyopathy, Familial Restrictive, 2", "cardiomyopathy, familial restrictive, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiomyopathy, familial restrictive, 2", "shortest_name_length": 4}
{"curie": "MONDO:0004377", "names": ["non-functional pancreatic Delta cell NET", "Non-Functional Pancreatic Delta Cell NET", "pancreatic non-functioning delta cell tumor", "Non-Functioning Pancreatic Delta Cell Tumor", "non-functioning pancreatic Delta cell tumor", "non-functioning pancreatic Delta cell neoplasm", "Non-Functioning Pancreatic Delta Cell Neoplasm", "Nonfunctional Pancreatic Delta Cell Neuroendocrine Tumor", "nonfunctional Pancreatic Delta cell Neuroendocrine tumor", "non-functional pancreatic Delta cell neuroendocrine tumor", "Nonfunctioning Pancreatic Delta Cell Neuroendocrine Tumor", "Non-Functional Pancreatic Delta Cell Neuroendocrine Tumor", "Non-Functioning Pancreatic Delta Cell Neuroendocrine Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic non-functioning delta cell tumor", "shortest_name_length": 40}
{"curie": "MONDO:0014621", "names": ["BRGDA9", "Brugada syndrome 9", "BRUGADA SYNDROME 9", "KCND3 Brugada syndrome", "Brugada syndrome type 9", "Brugada syndrome caused by mutation in KCND3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brugada syndrome 9", "shortest_name_length": 6}
{"curie": "MONDO:0017776", "names": ["nocardiosis", "NOCARDIOSIS", "Nocardioses", "Nocardiosis", "Nocardiosis NOS", "Nocardiosis, NOS", "lung nocardiosis", "nocardia infection", "Nocardia infection", "Nocardia Infection", "Nocardia Infections", "Nocardia; infection", "Nocardia infections", "nocardia infections", "infection; Nocardia", "Infection, Nocardia", "Nocardial Infection", "Infections, Nocardia", "Nocardiosis (disorder)", "nocardiosis (diagnosis)", "Nocardiosis, unspecified", "Nocardia infectious disease", "Nocardia disease or disorder", "Nocardia caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nocardiosis", "shortest_name_length": 11}
{"curie": "UMLS:C0332534", "names": ["induration", "Induration", "indurations", "Scirrhous response", "Induration (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Induration", "shortest_name_length": 10}
{"curie": "UMLS:C1096278", "names": ["Anterior chamber inflammation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anterior chamber inflammation", "shortest_name_length": 29}
{"curie": "MONDO:0006621", "names": ["vulvar inverted follicular keratosis", "Vulvar Inverted Follicular Keratosis", "mammalian vulva inverted follicular keratosis", "inverted follicular keratosis of mammalian vulva"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar inverted follicular keratosis", "shortest_name_length": 36}
{"curie": "MONDO:0004679", "names": ["Leukoplakia;vagina", "vaginal leukoplakia", "vagina; leukoplakia", "Vaginal Leukoplakia", "vaginal Leukoplakia", "leukoplakia; vagina", "Vaginal leukoplakia", "Leucoplakia of vagina", "Leukoplakia of Vagina", "Leukoplakia of vagina", "leukoplakia of vagina", "leukoplakia of the vagina", "Leukoplakia of the Vagina", "vaginal leukoplakia (diagnosis)", "Leukoplakia of vagina (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukoplakia of vagina", "shortest_name_length": 18}
{"curie": "MONDO:0031230", "names": ["mitochondrial complex II deficiency, nuclear type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex II deficiency, nuclear type", "shortest_name_length": 49}
{"curie": "MONDO:0011183", "names": ["PDB2", "Paget disease of bone-2", "Paget's disease of bone 2", "Paget disease of bone 2, early-onset", "PAGET DISEASE OF BONE 2, EARLY-ONSET"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paget disease of bone 2, early-onset", "shortest_name_length": 4}
{"curie": "MONDO:0018239", "names": ["aggrecan-related bone disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aggrecan-related bone disorder", "shortest_name_length": 30}
{"curie": "UMLS:C4329638", "names": ["CNS Solitary Fibrous Tumor, Grade 1", "Central Nervous System Solitary Fibrous Tumor", "Central Nervous System Solitary Fibrous Tumor, Grade 1", "CNS Solitary Fibrous Tumor/Hemangiopericytoma, Grade 1", "Solitary fibrous tumor/hemangiopericytoma Grade 1 (CNS)", "Central Nervous System Solitary Fibrous Tumor/Hemangiopericytoma, Grade 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Solitary Fibrous Tumor, Grade 1", "shortest_name_length": 35}
{"curie": "UMLS:C4524682", "names": ["Lung Carcinoma Metastatic in the CNS", "Metastatic Lung Cancer in the Central Nervous System", "Lung Carcinoma Metastatic in the Central Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Carcinoma Metastatic in the Central Nervous System", "shortest_name_length": 36}
{"curie": "UMLS:C0349531", "names": ["Late gastric cancer", "LGC - Late gastric cancer", "Late gastric cancer (disorder)", "Late gastric cancer (diagnosis)", "gastric neoplasm malignant late cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Late gastric cancer", "shortest_name_length": 19}
{"curie": "UMLS:C3805283", "names": ["Administration site erythema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Administration site erythema", "shortest_name_length": 28}
{"curie": "MONDO:0001437", "names": ["PAP", "alveolar proteinosis", "proteinosis alveolar", "Alveolar proteinosis", "alveolar; proteinosis", "proteinosis; alveolar", "Proteinosis, alveolar", "LUNG, ALVEOLAR PROTEINOSIS", "Pulmonary Alveolar Proteinoses", "pulmonary alveolar proteinosis", "Pulmonary Alveolar Proteinosis", "Pulmonary alveolar proteinosis", "PULMONARY ALVEOLAR PROTEINOSIS", "Alveolar Proteinosis, Pulmonary", "Alveolar Proteinoses, Pulmonary", "Proteinosis, Pulmonary Alveolar", "Proteinoses, Pulmonary Alveolar", "Pulmonary alveolar lipoproteinosis", "PAP - Pulmonary alveolar proteinosis", "Intraalveolar phospholipid accumulation", "Pulmonary alveolar proteinosis (disorder)", "pulmonary alveolar proteinosis (diagnosis)", "Detection of PAS-positive extracellular material in broncho-alveolar lavage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary alveolar proteinosis", "shortest_name_length": 3}
{"curie": "MONDO:0045008", "names": ["cholesterol metabolism disease", "metabolic disorder; cholesterol", "cholesterol; metabolic disorder", "disorder of cholesterol metabolism", "Disorder of cholesterol metabolism", "cholesterol metabolic process disease", "disorder of cholesterol metabolic process", "Disorder of cholesterol metabolism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholesterol metabolism disease", "shortest_name_length": 30}
{"curie": "MONDO:0100515", "names": ["mirror movements 1 and/or agenesis of the corpus callosum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mirror movements 1 and/or agenesis of the corpus callosum", "shortest_name_length": 57}
{"curie": "MONDO:0014019", "names": ["DYT24", "DYT-ANO3", "dystonia 24", "DYSTONIA 24", "Dystonia 24", "dystonia type 24", "DYT24 - dystonia 24", "ANO3 dystonic disorder", "dystonic disorder caused by mutation in ANO3", "Cranio-cervical dystonia with laryngeal and upper limb involvement", "cranio-cervical dystonia with laryngeal and upper-limb involvement", "Cranio-cervical dystonia with laryngeal and upper-limb involvement", "Cranio-cervical dystonia with laryngeal and upper limb involvement (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dystonia 24", "shortest_name_length": 5}
{"curie": "MONDO:0012336", "names": ["CATCN2", "CTRCT22", "cataract 22", "cataract 22 multiple types", "cataract 22, multiple types", "CATARACT 22, MULTIPLE TYPES", "CRYBB3 early-onset non-syndromic cataract", "autosomal recessive congenital nuclear cataract 2", "cataract, congenital nuclear, autosomal recessive 2", "Cataract, Congenital Nuclear, Autosomal Recessive 2", "CATARACT, CONGENITAL NUCLEAR, AUTOSOMAL RECESSIVE 2", "early-onset non-syndromic cataract caused by mutation in CRYBB3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 22 multiple types", "shortest_name_length": 6}
{"curie": "MONDO:0001164", "names": ["sociopath", "Sociopath", "Psychopath", "sociopaths", "psychopath", "Sociopathy", "psychopathy", "Psychopathy", "psychopaths", "ASP disorder", "Asocial personality", "asocial personality", "Dyssocial personality", "dyssocial personality", "disorder; sociopathic", "sociopathic; disorder", "Antisocial Personality", "antisocial personality", "Psychopath.personality", "Antisocial personality", "psychopath.personality", "Personality;antisocial", "ANTISOCIAL PERSONALITY", "sociopathic personality", "antisocial; personality", "Sociopathic personality", "Sociopathic Personality", "Personality, Antisocial", "Personality, Sociopathic", "psychopathic personality", "Antisocial Personalities", "Psychopathic Personality", "Psychopathic personality", "sociopathic personalities", "Personality, Psychopathic", "Sociopathic Personalities", "Personalities, Antisocial", "psychopathic constitution", "Psychopathic Personalities", "Personalities, Sociopathic", "Personalities, Psychopathic", "personality disorder; asocial", "asocial; personality disorder", "dissocial personality disorder", "Dissocial personality disorder", "Asocial personality (disorder)", "personality disorder; dissocial", "Antisocial personality disorder", "disorder; dissocial personality", "dissocial personality; disorder", "dissocial; personality disorder", "antisocial personality disorder", "PERSONALITY DISORDER ANTISOCIAL", "Antisocial Personality Disorder", "Antisocial personality disorders", "Sociopathic personality disorder", "Personality Disorder, Antisocial", "Antisocial Personality Disorders", "personality disorder; antisocial", "antisocial personality disorders", "antisocial; personality disorder", "sociopathic personality disorder", "Disorder, Antisocial Personality", "Psychopathic personality disorder", "personality disorder; sociopathic", "sociopathic; personality disorder", "Disorders, Antisocial Personality", "psychopathic personality disorder", "Personality Disorders, Antisocial", "psychopathic; personality disorder", "Sociopathic personality (disorder)", "personality disorder; psychopathic", "Psychopathic personality (disorder)", "Antisocial personality disorder (disorder)", "antisocial personality disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "antisocial personality disorder", "shortest_name_length": 9}
{"curie": "UMLS:C3495808", "names": ["Subchorial Thrombus", "Subchorionic hematoma", "Subchorionic Hematoma", "Subchorionic haematoma", "Subchorionic hematoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subchorionic hematoma", "shortest_name_length": 19}
{"curie": "MONDO:0003730", "names": ["LEUKEMIA ALEUKEMIC", "leukemia aleukemic", "aleukemic myelosis", "Aleukemic Leukemia", "Leukemia aleukemic", "aleukemic leukemia", "Aleukemic leukemia", "aleukemic; leukemia", "leukemia; aleukemic", "Aleukaemic leukaemia", "subleukemic leukemia", "Aleukemic leukemia NOS", "Aleukemic leukemia, NOS", "Aleukaemic leukaemia NOS", "Aleukaemic leukaemia, NOS", "Aleukemic leukemia (disorder)", "aleukemic leukemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aleukemic leukemia", "shortest_name_length": 18}
{"curie": "UMLS:C1332592", "names": ["Borderline Breast Phyllodes Tumor", "Borderline Phyllodes Tumor of Breast", "Borderline Breast Phyllodes Neoplasm", "Phyllodes tumor of breast, borderline", "Phyllodes tumour of breast, borderline", "Borderline Phyllodes Neoplasm of Breast", "Borderline Phyllodes Tumor of the Breast", "Low Grade Malignant Breast Phyllodes Tumor", "Borderline Phyllodes Neoplasm of the Breast", "Phyllodes tumor of breast, borderline (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Breast Phyllodes Tumor", "shortest_name_length": 33}
{"curie": "UMLS:C0151735", "names": ["Injection Site Event", "Injection Site Events", "Injection site reaction", "reaction injection site", "Injection site disorder", "INJECTION SITE REACTION", "injection site reaction", "injection site disorder", "Injection Site Reaction", "Injection Site Reactions", "Injection site reactions", "injection reactions site", "INJECTION SITE DISORDERS", "Injection site reaction NOS", "Injection Site Adverse Event", "Injection site disorder, NOS", "REACTION INJECTION SITE (NOS)", "INJECTION SITE REACTION (NOS)", "Reaction injection site (NOS)", "Injection site disorder (disorder)", "injection site disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection Site Reaction", "shortest_name_length": 20}
{"curie": "UMLS:C1333515", "names": ["Extraskeletal Cartilaginous and Osseous Tumor", "Extraskeletal Cartilaginous and Osseous Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extraskeletal Cartilaginous and Osseous Neoplasm", "shortest_name_length": 45}
{"curie": "MONDO:0011479", "names": ["POTS", "Orthostasis", "soldiers heart", "SOLDIERS HEART", "Soldiers heart", "Irritable heart", "IRRITABLE HEART", "irritable heart", "Orthostatic intolerance", "orthostatic intolerance", "Orthostatic Intolerance", "ORTHOSTATIC INTOLERANCE", "orhtostatic intolerance", "Intolerance, Orthostatic", "neurocirculatory asthenia", "Postural Tachycardia Syndrome", "Postural tachycardia syndrome", "mitral valve prolapse syndrome", "Tachycardia Syndrome, Postural", "Syndrome, Postural Tachycardia", "Orthostatic intolerance (finding)", "postural orthostatic tachycardia syndrome", "Postural orthostatic tachycardia syndrome", "Postural Orthostatic Tachycardia Syndrome", "orthostatic intolerance due to NET deficiency", "Postural orthostatic tachycardia syndrome [POTS]", "POTS - postural orthostatic tachycardia syndrome", "postural tachycardia syndrome due to NET deficiency", "Postural orthostatic tachycardia syndrome (disorder)", "postural orthostatic tachycardia syndrome (diagnosis)", "familial orthostatic tachycardia due to norepinephrine transporter deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postural orthostatic tachycardia syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0035524", "names": ["BPES type 1", "blepharophimosis-ptosis-epicanthus inversus syndrome type 1", "blepharophimosis-ptosis-epicanthus inversus syndrome with premature ovarian failure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blepharophimosis-ptosis-epicanthus inversus syndrome type 1", "shortest_name_length": 11}
{"curie": "UMLS:C1334160", "names": ["Immunosuppression-Related Cancer", "Immunosuppression-Related Malignancy", "Immunodeficiency-Related Malignant Neoplasm", "Immunosuppression-Related Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immunodeficiency-Related Malignant Neoplasm", "shortest_name_length": 32}
{"curie": "MONDO:0021473", "names": ["benign epididymal tumor", "Benign Epididymal Tumor", "benign tumor of epididymis", "Benign tumor of epididymis", "Benign Tumor of Epididymis", "Benign Epididymal Neoplasm", "epididymis benign neoplasm", "benign epididymal neoplasm", "Benign tumour of epididymis", "benign neoplasm of epididymis", "Benign neoplasm of epididymis", "Benign Neoplasm of Epididymis", "Benign epididymal neoplasm NOS", "benign tumor of the epididymis", "Benign Tumor of the Epididymis", "Benign Neoplasm of the Epididymis", "benign neoplasm of the epididymis", "Benign neoplasm of epididymis (disorder)", "benign neoplasm of epididymis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of epididymis", "shortest_name_length": 23}
{"curie": "MONDO:0005401", "names": ["colon mass", "COLON TUMOR", "tumor colon", "Colon tumor", "colon tumor", "Colon Tumor", "colon tumors", "colonic mass", "Colonic mass", "colon masses", "Colon tumour", "colonic tumor", "Colonic Tumor", "colon tumours", "Colonic tumor", "colon neoplasm", "Colon Neoplasm", "tumor of colon", "Tumor of colon", "Colon neoplasm", "Tumor of Colon", "COLON NOS MASS", "Tumour of colon", "Colon neoplasia", "Colon Neoplasms", "colon neoplasms", "Neoplasm, Colon", "colonic neoplasm", "Colonic Neoplasm", "COLONIC NEOPLASM", "Neoplasms, Colon", "NEOPLASM OF COLON", "Neoplasm of colon", "Neoplasm of Colon", "Colonic Neoplasms", "colonic neoplasms", "Neoplasm, Colonic", "neoplasm of colon", "Colon neoplasm NOS", "colon cancer tumor", "tumor of the colon", "Tumor of the Colon", "colon tumor cancer", "Neoplasms, Colonic", "cancer colon tumors", "Colonic neoplasm NOS", "Neoplasm of the colon", "colon tumor or cancer", "neoplasm of the colon", "Neoplasm of the Colon", "colon neoplasm (disease)", "Neoplasm of colon (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colonic neoplasm", "shortest_name_length": 10}
{"curie": "UMLS:C5420302", "names": ["Unresectable Testicular Biphasic Mesothelioma", "Unresectable Paratesticular Biphasic Mesothelioma", "Unresectable Tunica Vaginalis Biphasic Mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Paratesticular Biphasic Mesothelioma", "shortest_name_length": 45}
{"curie": "MONDO:0020437", "names": ["PAVC", "PAVSD", "ostium primum", "Ostium primum", "ostium primum ASD", "Septum primum defect", "Ostium Primum Defect", "Ostium primum defect", "ASD ostium primum type", "ASD, ostium primum type", "Persistent Ostium Primum", "Persistent ostium primum", "Ostium Primum, Persistent", "Primum, Persistent Ostium", "persistent; ostium primum", "ostium primum; persistent", "Primum atrial septal defect", "Atrial septum primum defect", "primum atrial septal defect", "Ostium primum defect (disorder)", "Atrial septal defect, primum type", "ostium primum atrial septal defect", "atrial septal defect ostium primum", "Ostium primum atrial septal defect", "Atrial Septal Defect Ostium Primum", "Ostium Primum Atrial Septal Defect", "ATRIAL SEPTAL DEFECT OSTIUM PRIMUM", "Primum atrioventricular canal defect", "partial atrioventricular septal defect", "atrial septal defect, ostium primum type", "[OBSOLETE] Atrial Septal Defect Ostium Primum", "ostium primum atrial septal defect (diagnosis)", "atrioventricular defect with atrial shunting only", "partial atrioventricular septal defect: ostium primum type", "partial atrioventricular canal defect with isolated atrial component", "incomplete atrioventricular canal defect with isolated atrial component", "incomplete atrioventricular septal defect with isolated atrial component"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial septal defect, ostium primum type", "shortest_name_length": 4}
{"curie": "MONDO:0005461", "names": ["adenocarcinoma uterus", "uterus adenocarcinoma", "uterine adenocarcinoma", "adenocarcinoma uterine", "Uterine adenocarcinoma", "Adenocarcinoma of uterus", "adenocarcinoma of uterus", "adenocarcinoma endometrial", "endometrial adenocarcinoma", "endometrial adenoacanthoma", "adenocarcinoma endometrium", "Adenocarcinoma endometrial", "Endometrial adenocarcinoma", "endometrium adenocarcinoma", "Endometrial Adenocarcinoma", "ADENOCARCINOMA ENDOMETRIAL", "ENDOMETRIAL ADENOCARCINOMA", "Endometrial Adenoacanthoma", "adenocarcinomas endometrial", "ENDOMETRIUM, ADENOCARCINOMA", "adenocarcinoma of the uterus", "Adenocanthoma of Endometrium", "adenoacanthoma of the uterus", "Adenocarcinoma of endometrium", "UTERINE CANCER ADENOCARCINOMA", "uterus cancer, adenoacanthoma", "Adenocarcinoma of Endometrium", "uterus cancer, adenocarcinoma", "adenocarcinoma uterine cancer", "adenocarcinoma of endometrium", "uterine cancer, adenoacanthoma", "uterine cancer, adenocarcinoma", "Adenocanthoma of the Endometrium", "Adenocarcinoma of the Endometrium", "adenocarcinoma of the Endometrium", "adenocarcinoma of the endometrium", "endometrioid adenoma or carcinoma", "Adenocarcinoma of uterus (disorder)", "endometrioid adenomas and carcinomas", "adenocarcinoma of uterus (diagnosis)", "endometrioid carcinoma of Endometrium", "endometrioid carcinoma of endometrium", "uterine corpus cancer, adenoacanthoma", "adenocarcinoma, endometrial, malignant", "ADENOCARCINOMA, ENDOMETRIAL, MALIGNANT", "endometrial endometrioid adenocarcinoma", "Adenocarcinoma of endometrium (disorder)", "Adenocarcinoma of endometrium (diagnosis)", "Endometrial Adenocarcinoma, Not Otherwise Specified", "endometrioid adenomas and carcinomas (morphologic abnormality)", "endometrioid adenoma or carcinoma NOS (morphologic abnormality)", "Endometrial Endometrioid Adenocarcinoma with Squamous Differentiation", "endometrial endometrioid adenocarcinoma with squamous differentiation", "Endometrial Endometrioid Adenocarcinoma, Variant with Squamous Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometrium adenocarcinoma", "shortest_name_length": 21}
{"curie": "MONDO:0017950", "names": ["microcephalic primordial dwarfism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephalic primordial dwarfism", "shortest_name_length": 33}
{"curie": "MONDO:0016204", "names": ["Idiopathic copper-associated cirrhosis", "idiopathic copper-associated cirrhosis", "Idiopathic copper associated cirrhosis of liver", "Non-Wilsonian hepatic copper toxicosis of infancy and childhood", "non-Wilsonian hepatic copper toxicosis of infancy and childhood", "Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)", "Non-Wilsonian hepatic copper toxicosis of infancy and childhood (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic copper-associated cirrhosis", "shortest_name_length": 38}
{"curie": "UMLS:C2062905", "names": ["Left Main Coronary Artery Stenosis", "left main coronary artery stenosis", "left main coronary artery stenosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "left main coronary artery stenosis", "shortest_name_length": 34}
{"curie": "MONDO:0009345", "names": ["Histidinemia", "Histidinuria", "HISTIDINEMIA", "histidinemia", "histidinuria", "Histidinaemia", "HIS deficiency", "HAL deficiency", "HAL Deficiency", "HAL DEFICIENCY", "HIS DEFICIENCY", "Hal deficiency", "HYPERHISTIDINEMIA", "Hyperhistidinemia", "hyperhistidinemia", "HISTIDASE DEFICIENCY", "Histidase deficiency", "histidase deficiency", "Deficiency in Histidase", "Deficiency of histidase", "Histidinemia (disorder)", "histidinemia (diagnosis)", "Deficiency of histidinase", "High blood histidine level", "histidine ammonia-lyase deficiency", "HISTIDINE AMMONIA-LYASE DEFICIENCY", "Histidine ammonia-lyase deficiency", "Deficiency of histidine a-deaminase", "Deficiency of histidine ammonia-lyase", "Deficiency of histidine ammonia-lyase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "histidinemia", "shortest_name_length": 12}
{"curie": "UMLS:C5555079", "names": ["Central Chondrosarcoma, Grade 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Chondrosarcoma, Grade 2", "shortest_name_length": 31}
{"curie": "MONDO:0021275", "names": ["eyelid papilloma", "Eyelid Papilloma", "Papilloma of eyelid", "Blepharal papilloma", "papilloma of eyelid", "Papilloma of Eyelid", "papilloma of the eyelid", "Papilloma of the Eyelid", "Papilloma of eyelid (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papilloma of eyelid", "shortest_name_length": 16}
{"curie": "UMLS:C5556292", "names": ["Advanced Microsatellite Stable Ovarian Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Microsatellite Stable Ovarian Carcinoma", "shortest_name_length": 48}
{"curie": "MONDO:0014035", "names": ["MRD19", "NEDSDV", "MRD19, FORMERLY", "CTNNB1-related intellectual disability", "autosomal dominant mental retardation 19", "Mental Retardation, Autosomal Dominant 19", "mental retardation, autosomal dominant 19", "autosomal dominant intellectual disability 19", "intellectual disability, autosomal dominant 19", "mental retardation, autosomal dominant type 19", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 19, FORMERLY", "intellectual disability, autosomal dominant type 19", "autosomal dominant intellectual developmental disorder 19", "autosomal dominant non-syndromic intellectual disability 19", "neurodevelopmental disorder with spastic diplegia and visual defects", "Neurodevelopmental Disorder with Spastic Diplegia and Visual Defects", "NEURODEVELOPMENTAL DISORDER WITH SPASTIC DIPLEGIA AND VISUAL DEFECTS", "severe intellectual disability-progressive spastic diplegia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe intellectual disability-progressive spastic diplegia syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0013369", "names": ["CMH7", "hypertrophic cardiomyopathy 7", "cardiomyopathy, hypertrophic, 7", "TNNI3 hypertrophic cardiomyopathy", "hypertrophic cardiomyopathy type 7", "cardiomyopathy, familial hypertrophic 7", "cardiomyopathy, familial hypertrophic, 7", "CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7", "Familial Hypertrophic Cardiomyopathy Type 7", "cardiomyopathy, familial hypertrophic, type 7", "hypertrophic cardiomyopathy caused by mutation in TNNI3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophic cardiomyopathy 7", "shortest_name_length": 4}
{"curie": "UMLS:C4763674", "names": ["Recurrent High Risk NMIBC", "Recurrent High Risk Non-Muscle Invasive Bladder Urothelial Carcinoma", "Recurrent High Risk, Non-Muscle Invasive Bladder Urothelial Carcinoma", "Recurrent High-Risk, Non-Muscle Invasive Bladder Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent High Risk Non-Muscle Invasive Bladder Urothelial Carcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0007654", "names": ["Genu valgum, st Helena familial", "hereditary pubertal genu valgum", "Hereditary pubertal genu valgum", "St. Helena familial genu valgum", "genu valgum, st Helena familial", "GENU VALGUM, ST. HELENA FAMILIAL", "genu valgum, st. Helena familial", "GENU VALGUM, HEREDITARY PUBERTAL", "Genu Valgum, St. Helena Familial", "genu valgum, hereditary pubertal", "Genu valgum, hereditary pubertal", "severe 'knock-knees' and variable lesser malalignment at the elbows and wrists"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genu valgum, st. Helena familial", "shortest_name_length": 31}
{"curie": "UMLS:C0279630", "names": ["Acute Eosinophilic Leukemia", "Adult Acute Eosinophilic Leukemia", "adult acute eosinophilic leukemia", "eosinophilic leukemia, adult acute", "leukemia, adult acute eosinophilic", "acute eosinophilic leukemia, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Acute Eosinophilic Leukemia", "shortest_name_length": 27}
{"curie": "MONDO:0010241", "names": ["CSNB2", "CSNB2A", "CSNB, incomplete, X-linked", "CSNB, Incomplete, X-Linked", "CSNB, INCOMPLETE, X-LINKED", "congenital stationary night blindness 2A", "CACNA1F congenital stationary night blindness", "congenital stationary night blindness type 2A", "night blindness, congenital stationary, type 2", "X-linked congenital stationary night blindness", "NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2", "Night Blindness, Congenital Stationary, Type 2", "congenital stationary night blindness - type 2a", "night blindness, congenital stationary, type 2A", "NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A", "Night Blindness, Congenital Stationary, Type 2A", "congenital stationary night blindness 2A X-linked", "congenital stationary night blindness - type 2a (diagnosis)", "night blindness, congenital stationary (incomplete), 2A, X-linked", "congenital stationary night blindness caused by mutation in CACNA1F"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital stationary night blindness 2A", "shortest_name_length": 5}
{"curie": "MONDO:0044351", "names": ["Schistosoma; intercalatum", "Infection by Schistosoma Intercalatum", "infection by Schistosoma intercalatum", "Infection by Schistosoma intercalatum", "schistosomiasis; Schistosoma intercalatum", "Schistosoma intercalatum infectious disease", "Infection caused by Schistosoma intercalatum", "Schistosoma intercalatum disease or disorder", "infection caused by Schistosoma intercalatum", "schistosomiasis due to Schistosoma intercalatum", "Schistosoma intercalatum caused disease or disorder", "Infection caused by Schistosoma intercalatum (disorder)", "schistosomiasis due to Schistosoma intercalatum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Schistosoma intercalatum infectious disease", "shortest_name_length": 25}
{"curie": "MONDO:0008371", "names": ["DDD1", "dark dot disease", "Dowling-Degos Disease", "Dowling-Degos disease", "Dowling-Degos disease 1", "Dowling-Degos disease type 1", "Dowling-Degos Kitamura disease", "reticular pigment anomaly of flexures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dowling-Degos disease", "shortest_name_length": 4}
{"curie": "UMLS:C5447283", "names": ["Unresectable Sinonasal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Sinonasal Squamous Cell Carcinoma", "shortest_name_length": 46}
{"curie": "MONDO:0012967", "names": ["Hemolytic anemia due to adenylate kinase deficiency", "hemolytic anemia due to adenylate kinase deficiency", "anemia hemolytic due to adenylate kinase deficiency", "Adenylate Kinase Deficiency, Hemolytic Anemia Due To", "ADENYLATE KINASE DEFICIENCY, HEMOLYTIC ANEMIA DUE TO", "ADENYLATE KINASE deficiency, hemolytic anemia due to", "Haemolytic anaemia due to adenylate kinase deficiency", "Hemolytic anemia due to adenylate kinase deficiency (disorder)", "Hemolytic anemia due to adenylate kinase deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemolytic anemia due to adenylate kinase deficiency", "shortest_name_length": 51}
{"curie": "UMLS:C0279087", "names": ["recurrent Kaposi sarcoma", "Recurrent Kaposi Sarcoma", "Recurrent Kaposi's Sarcoma", "Kaposi's sarcoma, recurrent", "sarcoma, Kaposi's, recurrent", "Recurrent Multiple Hemorrhagic Sarcoma", "recurrent multiple hemorrhagic sarcoma", "multiple hemorrhagic sarcoma, recurrent", "sarcoma, multiple hemorrhagic, recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Kaposi Sarcoma", "shortest_name_length": 24}
{"curie": "MONDO:0007368", "names": ["Familial benign hypocupremia", "familial benign hypocupremia", "Familial benign hypocupraemia", "Familial benign copper deficiency", "familial benign copper deficiency", "copper deficiency, familial benign", "Copper deficiency, familial benign", "COPPER DEFICIENCY, FAMILIAL BENIGN", "Familial benign copper deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial benign copper deficiency", "shortest_name_length": 28}
{"curie": "UMLS:C0155709", "names": ["fib/flutter", "fib flutter", "fib-flutter", "Flutter-fibrillation", "atrial fibrillation flutter", "atrial flutter fibrillation", "Atrial fibrillation/flutter", "Atrial flutter-fibrillation", "atrial flutter-fibrillation", "ATRIAL FLUTTER/ FIBRILLATION", "atrial fibrillation fluttering", "atrial fibrillation and flutter", "Atrial fibrillation and flutter", "Atrial fibrillation and flutter (disorder)", "atrial fibrillation and flutter (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atrial fibrillation and flutter", "shortest_name_length": 11}
{"curie": "MONDO:0014337", "names": ["CDCBM5", "TUBB2A Tubulinopathy", "complex cortical dysplasia with other brain malformations 5", "Complex Cortical Dysplasia with other Brain Malformations 5", "CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 5", "cortical dysplasia, complex, with other brain malformations 5", "complex cortical dysplasia with other brain malformations type 5", "TUBB2A complex cortical dysplasia with other brain malformations", "cortical dysplasia, Complex, with Other brain malformations type 5", "complex cortical dysplasia with other brain malformations caused by mutation in TUBB2A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complex cortical dysplasia with other brain malformations 5", "shortest_name_length": 6}
{"curie": "MONDO:0043731", "names": ["Bone lysis", "osteolysis", "Osteolyses", "OSTEOLYSIS", "Osteolysis", "lytic lesion", "Lytic lesion", "LYTIC LESION", "lesions lytic", "Lytic lesions", "Bone dissolution", "Breakdown of bone", "Osteolytic lesion", "osteolytic lesion", "BONE LESION LYTIC", "Lytic Bone Lesion", "lytic bone lesion", "Osteolytic Lesion", "bone lesions lytic", "lesion; osteolytic", "osteolytic; lesion", "Osteolytic lesions", "lesions osteolytic", "Lytic lesion of bone", "Osteolysis (disorder)", "osteolysis (diagnosis)", "RESORPTION BONE INCREASED", "Resorption bone increased", "Increased bone resorption", "Osteolytic defects of bones", "Osteolysis, site unspecified", "Lytic Metastatic Bone Lesion", "Osteolysis, unspecified site", "lytic metastatic bone lesion", "Osteolysis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lytic metastatic bone lesion", "shortest_name_length": 10}
{"curie": "MONDO:0013372", "names": ["LQT5", "LQT5 syndrome", "LONG QT SYNDROME 5", "long QT syndrome 5", "Long Qt Syndrome 5", "Long QT Syndrome 5", "KCNE1 long QT syndrome", "long QT syndrome type 5", "LQT5 syndrome (diagnosis)", "long QT syndrome 2/5, digenic", "long QT syndrome caused by mutation in KCNE1", "LONG QT SYNDROME 5, ACQUIRED, SUSCEPTIBILITY TO", "long QT syndrome 5, acquired, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "long QT syndrome 5", "shortest_name_length": 4}
{"curie": "MONDO:0017954", "names": ["pyogenic autoinflammatory syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyogenic autoinflammatory syndrome", "shortest_name_length": 34}
{"curie": "MONDO:0016724", "names": ["PTPR", "papillary tumor of pineal region", "Papillary tumor of pineal region", "Papillary tumour of pineal region", "papillary tumor of the pineal region", "Papillary Tumor of the Pineal Region", "Papillary tumor of the pineal region", "Papillary tumour of the pineal region", "Papillary tumor of pineal region (disorder)", "papillary tumor of pineal region (diagnosis)", "Papillary tumor of the pineal region (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papillary tumor of the pineal region", "shortest_name_length": 4}
{"curie": "MONDO:0005043", "names": ["hyperplasia", "HYPERPLASIA", "Hyperplasia", "HYPERPLASIAS", "hyperplastic", "Hyperplasias", "Hyperplastic", "hyperplasias", "Hypercellular", "Hyperplasia NOS", "hypercellularity", "Hypercellularity", "Hyperplasia, NOS", "Cellular proliferation", "cellular proliferation", "Proliferation, cellular", "HYPERPLASIAS: GENERAL TERMS", "Hyperplasia (morphologic abnormality)", "abnormal enlargement of an organ or a tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperplasia", "shortest_name_length": 11}
{"curie": "UMLS:C0242786", "names": ["high risk pregancy", "Pregancy high risk", "High Risk Pregnancy", "Pregnancy;high risk", "pregnancy high risk", "high pregnancy risk", "PREGNANCY HIGH RISK", "high-risk pregnancy", "high risk pregnancy", "High-Risk Pregnancy", "Pregnancy high risk", "High risk pregnancy", "Pregnancy, High-Risk", "high pregnancy risks", "Pregnancy, High Risk", "Pregnancy, high risk", "pregnancy; high-risk", "High-Risk Pregnancies", "high-risk pregnancies", "high risk pregnancies", "High risk pregnancies", "high pregnancies risk", "Pregnancies, High-Risk", "HRP - High risk pregnancy", "High risk pregnancy (finding)", "finding of high risk pregnancy", "high-risk pregnancy (diagnosis)", "clinical finding pregnancy high risk", "PREGNANCY/OUTCOME AT RISK: (HIGH RISK)", "finding of high risk pregnancy (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High-Risk Pregnancy", "shortest_name_length": 18}
{"curie": "MONDO:0015892", "names": ["GHIS", "Laron dwarfism", "laron dwarfism", "LARON SYNDROME", "Laron Syndrome", "Laron syndrome", "Laron Dwarfism", "Dwarfism, Laron", "Syndrome, Laron", "laron type dwarfism", "Laron-type dwarfism", "laron-type dwarfism", "dwarfism; Laron-type", "Laron-type; dwarfism", "Laron dwarf syndrome", "Pituitary Dwarfism II", "Primary GH resistance", "Laron Type Dwarfism I", "Primary GH Resistance", "PITUITARY DWARFISM II", "Dwarfism II, Pituitary", "GH receptor deficiency", "Pituitary Dwarfism IIs", "GH Resistance, Primary", "Dwarfism IIs, Pituitary", "Severe GH Insensitivity", "Laron type short stature", "Primary GH insensitivity", "short; stature, Laron-type", "stature; short, Laron-type", "Laron-type pituitary dwarfism", "Growth Hormone Receptor Defect", "Primary Growth Hormone Resistance", "Primary growth hormone resistance", "Growth Hormone Receptor Deficiency", "GROWTH HORMONE RECEPTOR DEFICIENCY", "Growth hormone receptor deficiency", "Laron type short stature (diagnosis)", "Primary growth hormone insensitivity", "GROWTH HORMONE INSENSITIVITY SYNDROME", "Complete growth hormone insensitivity", "growth hormone insensitivity syndrome", "Growth Hormone Insensitivity Syndrome", "Growth hormone insensitivity syndrome", "Growth hormone insensitivity syndromes", "Growth Hormone Insensitivity Syndromes", "Laron-type isolated somatotropin defect", "Growth hormone receptor disorder syndrome", "Short stature due to growth hormone resistance", "Laron-type isolated somatotropin defect (disorder)", "short stature due to a defect in growth hormone receptor or post-receptor pathway", "Short stature due to a defect in growth hormone receptor or post-receptor pathway"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "growth hormone insensitivity syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0019915", "names": ["UPD(14)mat", "maternal uniparental disomy of chromosome 14", "maternal uniparental disomy of chromosome type 14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maternal uniparental disomy of chromosome 14", "shortest_name_length": 10}
{"curie": "UMLS:C0014458", "names": ["Weingarten", "Eosinophilic lung", "eosinophilic lung", "WEINGARTEN SYNDROME", "tropical eosinophilia", "Weingarten's syndrome", "Tropical eosinophilia", "Tropical Eosinophilia", "tropical; eosinophilia", "Tropical Eosinophilias", "EOSINOPHILIA, TROPICAL", "eosinophilia; tropical", "Eosinophilia, Tropical", "Filarial hypereosinophilia", "tropical pulmonary eosinophilia", "Tropical pulmonary eosinophilia", "eosinophilia pulmonary tropical", "Weingarten's syndrome (diagnosis)", "tropical eosinophilia (diagnosis)", "Tropical (pulmonary) eosinophilia NOS", "Tropical pulmonary eosinophilia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eosinophilia, Tropical", "shortest_name_length": 10}
{"curie": "MONDO:0019947", "names": ["RMD2", "LGMD1C", "LGMD1C, FORMERLY", "Rippling Muscle Disease 2", "RIPPLING MUSCLE DISEASE 2", "rippling muscle disease 2", "CAV3 rippling muscle disease", "rippling muscle disease type 2", "RIPPLING MUSCLE DISEASE 2 (disorder)", "muscular dystrophy limb-girdle type IC", "limb-girdle muscular dystrophy type 1C", "muscular dystrophy, limb-girdle, type 1C", "muscular dystrophy, limb-girdle, type IC", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1C, FORMERLY", "rippling muscle disease caused by mutation in CAV3", "CAV3 autosomal dominant limb-girdle muscular dystrophy", "autosomal dominant limb-girdle muscular dystrophy type 1C", "limb-girdle muscular dystrophy due to caveolin-3 deficiency", "autosomal dominant limb-girdle muscular dystrophy caused by mutation in CAV3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rippling muscle disease 2", "shortest_name_length": 4}
{"curie": "UMLS:C1335708", "names": ["Gastric malignancy recurrent", "Recurrent Malignant Gastric Neoplasm", "Malignant neoplasm of stomach recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant neoplasm of stomach recurrent", "shortest_name_length": 28}
{"curie": "UMLS:C1336403", "names": ["Stage IVC Mouth Mucoepidermoid Carcinoma", "Stage IVC Oral Cavity Mucoepidermoid Cancer", "Stage IVC Mucoepidermoid Carcinoma of Mouth", "Stage IVC Oral Cavity Mucoepidermoid Carcinoma", "Stage IVC Mucoepidermoid Carcinoma of the Mouth", "Stage IVC Mucoepidermoid Carcinoma of Oral Cavity", "Stage IVC Mucoepidermoid Carcinoma of the Oral Cavity", "Stage IVC Oral Cavity Mucoepidermoid Carcinoma AJCC v6", "Stage IVC Oral Cavity Mucoepidermoid Carcinoma AJCC v7", "Stage IVC Oral Cavity Mucoepidermoid Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Oral Cavity Mucoepidermoid Carcinoma AJCC v6 and v7", "shortest_name_length": 40}
{"curie": "UMLS:C0279749", "names": ["salivary gland anaplastic carcinoma", "Anaplastic Salivary Gland Carcinoma", "Salivary Gland Anaplastic Carcinoma", "anaplastic carcinoma, salivary gland", "Undifferentiated Salivary Gland Cancer", "anaplastic carcinoma of salivary gland", "Anaplastic Carcinoma of Salivary Gland", "Undifferentiated Salivary Gland Carcinoma", "Salivary Gland Undifferentiated Carcinoma", "Anaplastic Carcinoma of the Salivary Gland", "undifferentiated carcinoma, salivary gland", "carcinoma of the salivary gland, anaplastic", "Undifferentiated Carcinoma of Salivary Gland", "undifferentiated carcinoma of salivary gland", "cancer of the salivary gland, undifferentiated", "Undifferentiated Carcinoma of the Salivary Gland", "anaplastic carcinoma of salivary gland (diagnosis)", "undifferentiated carcinoma of salivary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anaplastic carcinoma of salivary gland", "shortest_name_length": 35}
{"curie": "MONDO:0002862", "names": ["bile duct sarcoma", "sarcoma of bile duct", "sarcoma of the bile duct"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bile duct sarcoma", "shortest_name_length": 17}
{"curie": "MONDO:0060677", "names": ["chromosome 1p35 deletion syndrome", "CHROMOSOME 1p35 DELETION SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 1p35 deletion syndrome", "shortest_name_length": 33}
{"curie": "MONDO:0020196", "names": ["anomaly of the secretory and excretory apparatus of the lacrimal system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anomaly of the secretory and excretory apparatus of the lacrimal system", "shortest_name_length": 71}
{"curie": "MONDO:0009969", "names": ["renal-genital-middle ear anomalies", "renal genital middle ear anomalies", "renal, genital, and middle EAR anomalies", "Renal, Genital, and Middle Ear Anomalies", "RENAL, GENITAL, AND MIDDLE EAR ANOMALIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal-genital-middle ear anomalies", "shortest_name_length": 34}
{"curie": "UMLS:C0334304", "names": ["Adenocarcinoma in situ in villous adenoma", "Adenocarcinoma In Situ in Villous Adenoma", "adenocarcinoma in situ in villous adenoma", "Adenocarcinoma in situ in villous adenoma (disorder)", "adenocarcinoma in situ in villous adenoma (diagnosis)", "Adenocarcinoma in situ in villous adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma in situ in villous adenoma", "shortest_name_length": 41}
{"curie": "MONDO:0009400", "names": ["HPI", "HYRPRO1", "PRODH hyperprolinemia", "Hyperprolinemia type 1", "type I hyperprolinemia", "Hyperprolinemia type I", "hyperprolinemia type 1", "hyperprolinemia type I", "Hyperprolinemia, type I", "hyperprolinemia, type 1", "HYPERPROLINEMIA, TYPE I", "hyperprolinemia, type I", "Hyperprolinaemia type I", "Hyperprolinaemia, type I", "proline oxidase deficiency", "Proline oxidase deficiency", "PROLINE OXIDASE DEFICIENCY", "Proline dehydrogenase deficiency", "type I hyperprolinemia (diagnosis)", "hyperprolinemia caused by mutation in PRODH", "Proline dehydrogenase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperprolinemia type 1", "shortest_name_length": 3}
{"curie": "MONDO:0003700", "names": ["Brachial Plexus Tumor", "brachial plexus tumor", "Tumor of Brachial Plexus", "Brachial Plexus Neoplasm", "tumor of brachial plexus", "brachial plexus neoplasm", "brachial plexus neoplasms", "Brachial Plexus Neoplasms", "neoplasm of brachial plexus", "brachial nerve plexus tumor", "Neoplasm of Brachial Plexus", "tumor of the brachial plexus", "Tumor of the Brachial Plexus", "tumor of the Brachial Plexus", "brachial nerve plexus neoplasm", "tumor of brachial nerve plexus", "Neoplasm of the Brachial Plexus", "neoplasm of the brachial plexus", "neoplasm of brachial nerve plexus", "brachial nerve plexus neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachial plexus neoplasm", "shortest_name_length": 21}
{"curie": "UMLS:C0751857", "names": ["Mercurial Neuroanesthenia", "Neuroanesthenia, Mercurial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mercurial Neuroanesthenia", "shortest_name_length": 25}
{"curie": "MONDO:0008986", "names": ["Circumvallate Placenta Syndrome", "circumvallate placenta syndrome", "CIRCUMVALLATE PLACENTA SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "circumvallate placenta syndrome", "shortest_name_length": 31}
{"curie": "UMLS:C4288305", "names": ["Recurrent Glioblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Glioblastoma", "shortest_name_length": 22}
{"curie": "MONDO:0044349", "names": ["acquired hemoglobinopathy", "Acquired hemoglobinopathy", "Acquired haemoglobinopathy", "Acquired hemoglobinopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired hemoglobinopathy", "shortest_name_length": 25}
{"curie": "UMLS:C0751249", "names": ["Chronic Insomnia", "Chronic insomnia", "chronic insomnia", "insomnia chronic", "Insomnia, Chronic", "Chronic insomnia (disorder)", "Chronic insomnia (diagnosis)", "sleep disorder insomnia chronic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic Insomnia", "shortest_name_length": 16}
{"curie": "UMLS:C0404852", "names": ["Vanishing Twin", "Vanishing Twin Syndrome", "Vanishing twin syndrome", "Vanishing twin syndrome (disorder)", "Vanishing twin syndrome (diagnosis)", "spontaneous abortion vanishing twin syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vanishing twin syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C0278559", "names": ["esophageal cancer stage I", "Stage I Esophageal Cancer", "stage I esophageal cancer", "esophagus cancer, stage I", "esophageal cancer, stage I", "stage I cancer of the esophagus", "Stage I Esophageal Cancer AJCC v6", "Esophageal Cancer Stage I AJCC v6", "Stage I Esophagus Carcinoma AJCC v6", "Stage I Esophageal Carcinoma AJCC v6", "Stage I Carcinoma of Esophagus AJCC v6", "Stage I Carcinoma of the Esophagus AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Esophageal Cancer", "shortest_name_length": 25}
{"curie": "MONDO:0016707", "names": ["AstB", "astroblastoma", "Astroblastoma", "Astroblastomas", "cerebral astroblastoma", "Astroblastoma, MN1-Altered", "Astroblastoma (morphologic abnormality)", "astroblastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "astroblastoma", "shortest_name_length": 4}
{"curie": "UMLS:C0017571", "names": ["Gingival Pocket", "Gingival pocket", "GINGIVAL POCKETS", "Gingival pockets", "Pocket, Gingival", "Gingival Pockets", "Pockets, Gingival", "Gingival pocket (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gingival Pocket", "shortest_name_length": 15}
{"curie": "UMLS:C1332638", "names": ["Breast Small Cell Carcinoma", "Oat Cell Carcinoma of Breast", "Small Cell Carcinoma of Breast", "small cell carcinoma of breast", "Oat Cell Carcinoma of the Breast", "Small Cell Carcinoma of the Breast", "Breast Small Cell Neuroendocrine Carcinoma", "small cell carcinoma of breast (diagnosis)", "Small Cell Neuroendocrine Carcinoma of Breast", "Small Cell Neuroendocrine Carcinoma of the Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small cell carcinoma of breast", "shortest_name_length": 27}
{"curie": "MONDO:0021372", "names": ["temporal lobe tumor", "Temporal Lobe Tumor", "Tumor of Temporal Lobe", "tumor of temporal lobe", "temporal lobe neoplasm", "Temporal Lobe Neoplasm", "neoplasm of temporal lobe", "Neoplasm of temporal lobe", "Neoplasm of Temporal Lobe", "tumor of the temporal lobe", "Tumor of the Temporal Lobe", "Neoplasm of the Temporal Lobe", "neoplasm of the temporal lobe", "temporal lobe neoplasm (disease)", "neoplasm of temporal lobe of brain", "Neoplasm of temporal lobe (disorder)", "neoplasm of temporal lobe of brain (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplasm of temporal lobe", "shortest_name_length": 19}
{"curie": "MONDO:0005104", "names": ["AJCC G1 Sarcoma", "aJCC G1 sarcoma", "aJCC grade 1 sarcoma", "AJCC Grade I Sarcoma", "AJCC Grade 1 Sarcoma", "aJCC grade I sarcoma", "Well Differentiated Sarcoma", "well-differentiated sarcoma", "well differentiated sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aJCC grade 1 sarcoma", "shortest_name_length": 15}
{"curie": "UMLS:C4551678", "names": ["Eye inflammation", "EYE INFLAMMATION", "inflammation eye", "Inflammation;eye", "eye inflammation", "eyes inflammation", "eye inflammations", "Eye--Inflammation", "Eye inflammation NOS", "inflammation of the eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eye inflammation", "shortest_name_length": 16}
{"curie": "MONDO:0018610", "names": ["early-onset posterior subcapsular cataract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early-onset posterior subcapsular cataract", "shortest_name_length": 42}
{"curie": "UMLS:C0269932", "names": ["Puerperal Endometritis", "puerperal endometritis", "Endometritis;puerperal", "Puerperal endometritis", "Postpartum Endometritis", "ENDOMETRITIS POSTPARTUM", "endometritis; puerperal", "endometritis postpartum", "puerperal; endometritis", "POSTPARTUM ENDOMETRITIS", "Endometritis postpartum", "postpartum endometritis", "Puerperal Endomyometritis", "Puerperal endometritis (disorder)", "puerperal endometritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Puerperal endometritis", "shortest_name_length": 22}
{"curie": "UMLS:C0343640", "names": ["Endemic", "African Lymphoma", "African lymphoma", "AFRICAN LYMPHOMA", "Lymphoma, African", "Endemic Burkitt Lymphoma", "African Burkitt lymphoma", "Endemic Burkitt lymphoma", "African Burkitt Lymphoma", "Endemic Burkitt's Lymphoma", "African Burkitt's Lymphoma", "African Burkitt's lymphoma", "Endemic Burkitt's lymphoma", "African Burkitt's lymphoma (disorder)", "African Burkitt's lymphoma (diagnosis)", "Endemic Burkitt's lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "African Burkitt's lymphoma", "shortest_name_length": 7}
{"curie": "UMLS:C4520719", "names": ["stage IIIA anal cancer", "Stage IIIA Anal Canal Cancer", "Stage IIIA Anal Canal Cancer AJCC v7", "Stage IIIA Anal Canal Cancer AJCC v6", "Stage IIIA Anal Carcinoma AJCC v6 and v7", "Stage IIIA Anal Canal Cancer AJCC v6 and v7", "Stage IIIA Anal Canal Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Anal Canal Cancer AJCC v6 and v7", "shortest_name_length": 22}
{"curie": "MONDO:0011624", "names": ["TALDOD", "Eyaid syndrome", "EYAID SYNDROME", "TALDO DEFICIENCY", "TALDO deficiency", "Taldo deficiency", "Transaldolase deficiency", "TRANSALDOLASE DEFICIENCY", "Transaldolase Deficiency", "transaldolase deficiency", "Deficiency of transaldolase", "Deficiency of glycerone-transferase", "Deficiency of transaldolase (disorder)", "Deficiency of dihydroxyacetonetransferase"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transaldolase deficiency", "shortest_name_length": 6}
{"curie": "MONDO:0011042", "names": ["Martínez-Frías syndrome", "Martinez-Frias Syndrome", "Martinez-Frias syndrome", "MARTINEZ-FRIAS SYNDROME", "Martinez Frias syndrome", "Diabetes, Neonatal, with Pancreatic Hypoplasia, Intestinal Atresia, and Gallbladder Aplasia or Hypoplasia", "pancreatic hypoplasia, intestinal atresia, and gallbladder aplasia or hypoplasia, with or without tracheoesophageal fistula", "PANCREATIC HYPOPLASIA, INTESTINAL ATRESIA, AND GALLBLADDER APLASIA OR HYPOPLASIA, WITH OR WITHOUT TRACHEOESOPHAGEAL FISTULA", "Pancreatic Hypoplasia, Intestinal Atresia, and Gallbladder Aplasia or Hypoplasia, with or without Tracheoesophageal Fistula"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Martinez-Frias syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0017926", "names": ["paraganglioma-somatostatinoma-polycythemia syndrome", "multiple paragangliomas associated with polycythemia", "multiple paragangliomas associated with erythrocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple paragangliomas associated with polycythemia", "shortest_name_length": 51}
{"curie": "UMLS:C0854826", "names": ["T-Cell Lymphoma Relapsed", "Relapsed T-Cell Lymphoma", "Recurrent T-Cell Lymphoma", "T-Cell Lymphoma Recurrent", "T-cell lymphoma recurrent", "T-cell lymphoma NOS recurrent", "Recurrent T-Cell Non-Hodgkin Lymphoma", "Recurrent T-Cell Non-Hodgkin's Lymphoma", "Recurrent T-Cell and NK-Cell Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-cell lymphoma recurrent", "shortest_name_length": 24}
{"curie": "UMLS:C0234119", "names": ["NM blockade", "Muscle blockade", "muscle relaxation", "Muscle relaxation", "Neuromuscular block", "NEUROMUSCULAR BLOCK", "BLOCK NEUROMUSCULAR", "Neuromuscular blockade", "neuromuscular blockade", "blockades neuromuscular", "Neuromuscular inhibition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neuromuscular inhibition", "shortest_name_length": 11}
{"curie": "MONDO:0002582", "names": ["subacute leukemia", "leukemia subacute", "Subacute leukemia", "Subacute leukaemia", "subacute; leukemia", "leukemia; subacute", "Subacute leukemia NOS", "Subacute leukemia, NOS", "Subacute leukaemia NOS", "Subacute leukaemia, NOS", "Subacute leukemia (disorder)", "subacute leukemia (diagnosis)", "Subacute leukemia of unspecified cell type", "Subacute leukaemia of unspecified cell type", "Leukemia of unspecified cell type, subacute", "Leukaemia of unspecified cell type, subacute"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subacute leukemia", "shortest_name_length": 17}
{"curie": "MONDO:0016276", "names": ["high-grade neuroendocrine carcinoma of the cervix uteri", "poorly differentiated neuroendocrine cervical carcinoma", "high-grade neuroendocrine carcinoma of the uterine cervix", "poorly differentiated neuroendocrine carcinoma of the cervix uteri"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "high-grade neuroendocrine carcinoma of the cervix uteri", "shortest_name_length": 55}
{"curie": "MONDO:0018632", "names": ["Del(11)(q22.2q22.3)", "monosomy 11q22.2q22.3", "monosomy 11q22.2-q22.3", "11q22.2-q22.3 deletion syndrome", "11q22.2q22.3 microdeletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "11q22.2q22.3 microdeletion syndrome", "shortest_name_length": 19}
{"curie": "UMLS:C3852987", "names": ["Acute Mesenteric Arterial Thrombosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Mesenteric Arterial Thrombosis", "shortest_name_length": 36}
{"curie": "MONDO:0008081", "names": ["NF4", "Nf 4", "NF IV", "neurofibromatosis type 4", "neurofibromatosis type IV", "Atypical neurofibromatosis", "NEUROFIBROMATOSIS, ATYPICAL", "neurofibromatosis, atypical", "Neurofibromatosis, atypical", "neurofibromatosis, variant form(S) of", "NEUROFIBROMATOSIS, VARIANT FORM(S) OF", "Neurofibromatosis, variant form(s) of", "type IV neurofibromatosis of Riccardi", "Neurofibromatosis, type 4, of Riccardi", "neurofibromatosis, type IV, of Riccardi", "NEUROFIBROMATOSIS, TYPE IV, OF RICCARDI", "Neurofibromatosis, Type Iv, Of Riccardi", "neurofibromatosis, type IV, of RICCARDI"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurofibromatosis, type IV, of Riccardi", "shortest_name_length": 3}
{"curie": "MONDO:0044621", "names": ["trip(16)(p12.1p12.3)", "tetrasomy 16p12.1p12.3", "tetrasomy 16p12.1-p12.3", "16p12.1p12.3 triplication syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "16p12.1p12.3 triplication syndrome", "shortest_name_length": 20}
{"curie": "MONDO:0018437", "names": ["AML with NPM1 somatic mutations", "Acute myeloid leukemia with NPM1 somatic mutation", "Acute myeloid leukaemia with NPM1 somatic mutation", "acute myeloid leukemia with NPM1 somatic mutations", "leukemia AML with nucleophosmin 1 somatic mutation", "Acute myeloid leukemia with NPM1 somatic mutations", "Acute myeloid leukemia with nucleophosmin 1 somatic mutation", "Acute myeloid leukaemia with nucleophosmin 1 somatic mutation", "Acute myeloid leukemia with nucleophosmin 1 somatic mutation (disorder)", "Acute myeloid leukemia with nucleophosmin 1 somatic mutation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia with NPM1 somatic mutations", "shortest_name_length": 31}
{"curie": "MONDO:0010008", "names": ["SARCOS", "SARDHD", "Sarcosinuria", "sarcosinemia", "Sarcosinemia", "SARCOSINEMIA", "Sarcosinaemia", "SARD Deficiency", "SARD DEFICIENCY", "SARD deficiency", "SARDH DEFICIENCY", "SARDH Deficiency", "SARDH deficiency", "HYPERSARCOSINEMIA", "Hypersarcosinemia", "hypersarcosinemia", "Hypersarcosinaemia", "High plasma sarcosine levels", "hypersarcosinemia (diagnosis)", "Sarcosine dehydrogenase deficiency", "Demethylation defect of N-methylglycine", "demethylation defect of N-methylglycine", "Sarcosine dehydrogenase complex deficiency", "sarcosine dehydrogenase complex deficiency", "SARCOSINE DEHYDROGENASE COMPLEX DEFICIENCY", "Sarcosine dehydrogenase deficiency (disorder)", "Sarcosin dehydrogenase complex, deficiency of", "Sarcosine Dehydrogenase Complex, Deficiency Of", "Deficiency of the sarcosine dehydrogenase complex"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sarcosinemia", "shortest_name_length": 6}
{"curie": "MONDO:0021896", "names": ["anterior spinal artery stroke", "Anterior spinal artery stroke"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anterior spinal artery stroke", "shortest_name_length": 29}
{"curie": "UMLS:C1868693", "names": ["Localised intraabdominal fluid collection", "Localized intraabdominal fluid collection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localised intraabdominal fluid collection", "shortest_name_length": 41}
{"curie": "UMLS:C3899669", "names": ["Childhood Colorectal Carcinoma", "Colorectal (Colon or Rectal) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Colorectal Carcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0013220", "names": ["HFE2B", "hemochromatosis type 2B", "Hemochromatosis, Type 2B", "HEMOCHROMATOSIS, TYPE 2B", "hemochromatosis, type 2B", "HAMP hemochromatosis type 2", "hemochromatosis type 2 caused by mutation in HAMP"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemochromatosis type 2B", "shortest_name_length": 5}
{"curie": "UMLS:C5417717", "names": ["b-IHCA", "Beta-Catenin-Activated Inflammatory Hepatocellular Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Beta-Catenin-Activated Inflammatory Hepatocellular Adenoma", "shortest_name_length": 6}
{"curie": "UMLS:C1335013", "names": ["Non-Neoplastic Hair Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Hair Disorder", "shortest_name_length": 28}
{"curie": "MONDO:0010660", "names": ["MRX9", "MRX44", "XLID9", "X-linked mental retardation 9", "MENTAL RETARDATION, X-LINKED 9", "Mental Retardation, X-Linked 9", "X-linked mental retardation 44", "mental retardation, X-linked 9", "mental retardation, X-linked 44", "MENTAL RETARDATION, X-LINKED 44", "Mental Retardation, X-Linked 44", "intellectual disability, X-linked 9", "mental retardation, X-linked type 9", "intellectual disability, X-linked 44", "intellectual disability, X-linked type 9", "X-linked mental retardation 9 (MRX9, XLMR9)", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 9", "non-syndromic X-linked intellectual disability 9", "FTSJ1 non-syndromic X-linked intellectual disability", "intellectual developmental disorder, X-linked 9, X-linked recessive", "non-syndromic X-linked intellectual disability caused by mutation in FTSJ1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 9", "shortest_name_length": 4}
{"curie": "MONDO:0010416", "names": ["Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities", "deafness, cataract, retinitis pigmentosa, and sperm abnormalities", "DEAFNESS, CATARACT, RETINITIS PIGMENTOSA, AND SPERM ABNORMALITIES", "deafness, cataract, retinitis pigmentosa, and sperm abnormalities, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness, cataract, retinitis pigmentosa, and sperm abnormalities", "shortest_name_length": 65}
{"curie": "MONDO:0016470", "names": ["EDS/OI syndrome", "OI-EDS Combined Syndrome", "Ehlers-Danlos/osteogenesis imperfecta syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ehlers-Danlos/osteogenesis imperfecta syndrome", "shortest_name_length": 15}
{"curie": "UMLS:C0521854", "names": ["Decreased drug tolerance", "Drug tolerance decreased", "Decreased drug tolerance (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Decreased drug tolerance", "shortest_name_length": 24}
{"curie": "MONDO:0014192", "names": ["CILD22", "primary ciliary dyskinesia 22", "CILIARY DYSKINESIA, PRIMARY, 22", "ciliary dyskinesia, primary, 22", "primary ciliary dyskinesia type 22", "ZMYND10 primary ciliary dyskinesia", "ciliary dyskinesia, primary, type 22", "primary ciliary dyskinesia caused by mutation in ZMYND10", "primary ciliary dyskinesia 22 with or without situs inversus", "ciliary dyskinesia, primary, 22, with or without situs inversus", "CILIARY DYSKINESIA, PRIMARY, 22, WITH OR WITHOUT SITUS INVERSUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia 22", "shortest_name_length": 6}
{"curie": "UMLS:C5237418", "names": ["Refractory Merkel Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Merkel Cell Carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0017451", "names": ["short fingers", "manus non-syndromic brachydactyly", "non-syndromic brachydactyly of manus", "non-syndromic brachydactyly of fingers"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-syndromic brachydactyly of fingers", "shortest_name_length": 13}
{"curie": "MONDO:0100001", "names": ["AGS", "red meat allergy", "alpha-gal allergy", "alpha-gal syndrome", "tick bite meat allergy", "allergic galactose-alpha-1,3-galactose disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alpha-gal syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C5444131", "names": ["HNPP", "Neuropathy, Recurrent, with Pressure Palsies", "Hereditary Neuropathy with Liability to Pressure Palsies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neuropathy, Recurrent, with Pressure Palsies", "shortest_name_length": 4}
{"curie": "MONDO:0013169", "names": ["dup(5)(p13)", "trisomy 5p13", "5p13 microduplication syndrome", "CHROMOSOME 5p13 DUPLICATION SYNDROME", "chromosome 5p13 duplication syndrome", "Chromosome 5p13 Duplication Syndrome", "chromosome 5p13 duplication syndrome, isolated cases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 5p13 duplication syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0014025", "names": ["SMAJ", "spinal muscular atrophy, Jokela type", "SPINAL MUSCULAR ATROPHY, JOKELA TYPE", "lower motor neuron syndrome with late-adult onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lower motor neuron syndrome with late-adult onset", "shortest_name_length": 4}
{"curie": "MONDO:0018162", "names": ["serine deficiency", "neurometabolic disorder due to serine deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurometabolic disorder due to serine deficiency", "shortest_name_length": 17}
{"curie": "UMLS:C2828179", "names": ["stage IIIC uterine sarcoma", "Stage IIIC Uterine Sarcoma", "Stage IIIC Uterine Sarcoma AJCC v7", "stage IIIC uterine sarcoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Uterine Sarcoma AJCC v7", "shortest_name_length": 26}
{"curie": "MONDO:0007479", "names": ["dwarfism Levi type", "dwarfism, Levi type", "DWARFISM, LEVI TYPE", "Dwarfism, Levi Type", "dwarfism Levi's type", "snub-nosed type of dwarfism", "Snub-Nosed Type of Dwarfism", "SNUB-NOSED TYPE OF DWARFISM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dwarfism, Levi type", "shortest_name_length": 18}
{"curie": "UMLS:C0751511", "names": ["Subwakefullness Syndrome", "Subwakefullness Syndromes", "Syndrome, Subwakefullness", "Syndromes, Subwakefullness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subwakefullness Syndrome", "shortest_name_length": 24}
{"curie": "UMLS:C1390523", "names": ["Musculoskeletal Complication", "musculoskeletal complications", "complications; musculoskeletal", "musculoskeletal; complications"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Musculoskeletal Complication", "shortest_name_length": 28}
{"curie": "UMLS:C4744381", "names": ["Benign Skull Base Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Skull Base Neoplasm", "shortest_name_length": 26}
{"curie": "MONDO:0016266", "names": ["endometrial squamous cell carcinoma", "body of uterus squamous cell carcinoma", "squamous cell carcinoma of the corpus uteri"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "squamous cell carcinoma of the corpus uteri", "shortest_name_length": 35}
{"curie": "MONDO:0011028", "names": ["LGMDR6", "LGMD2F", "LGMD type 2F", "delta-sarcoglycanopathy", "Delta-sarcoglycanopathy", "Delta-sarcoglycan-related LGMD R6", "Limb-girdle muscular dystrophy type 2F", "Limb girdle muscular dystrophy type 2F", "limb-girdle muscular dystrophy type 2F", "muscular dystrophy, limb-girdle, type 2F", "Muscular Dystrophy, Limb-Girdle, Type 2F", "LGMD due to delta-sarcoglycan deficiency", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2F", "muscular dystrophy, limb-girdle, autosomal recessive 6", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 6", "SGCD autosomal recessive limb-girdle muscular dystrophy", "Autosomal recessive limb-girdle muscular dystrophy type 2F", "autosomal recessive limb-girdle muscular dystrophy type 2F", "Autosomal recessive limb girdle muscular dystrophy type 2F", "Delta-sarcoglycan-related limb-girdle muscular dystrophy R6", "Muscular dystrophy limb-girdle with delta-sarcoglyan deficiency", "muscular dystrophy limb-girdle with delta-sarcoglyan deficiency", "limb-girdle muscular dystrophy due to delta-sarcoglycan deficiency", "Limb-girdle muscular dystrophy due to delta-sarcoglycan deficiency", "Limb girdle muscular dystrophy due to delta-sarcoglycan deficiency", "Autosomal recessive limb girdle muscular dystrophy type 2F (disorder)", "autosomal recessive limb-girdle muscular dystrophy caused by mutation in SGCD"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive limb-girdle muscular dystrophy type 2F", "shortest_name_length": 6}
{"curie": "UMLS:C5205069", "names": ["AdV Reactivation", "Adenovirus Reactivation", "Adenoviral Reactivation", "Adenovirus reactivation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenovirus reactivation", "shortest_name_length": 16}
{"curie": "UMLS:C0435750", "names": ["Closed fracture rib", "closed fracture of rib", "Closed fracture of rib", "Closed Fracture of Rib", "Closed fracture of ribs", "Fracture of ribs; closed", "Closed fracture of rib(s)", "Closed fracture of rib, NOS", "Closed fracture of rib (disorder)", "closed fracture of rib (diagnosis)", "Closed fracture of rib, unspecified", "Closed fracture of ribs, unspecified", "Closed fracture of rib(s), unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Closed fracture of rib", "shortest_name_length": 19}
{"curie": "UMLS:C1266123", "names": ["Angiomyofibroblastoma", "Angiomyofibroblastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Angiomyofibroblastoma", "shortest_name_length": 21}
{"curie": "MONDO:0006367", "names": ["Pharynx Adenoid Cystic Carcinoma", "pharynx adenoid cystic carcinoma", "Pharyngeal Adenoid Cystic Carcinoma", "adenoid cystic carcinoma of pharynx", "pharyngeal adenoid cystic carcinoma", "Adenoid Cystic Carcinoma of Pharynx", "pharyngeal throat adenoid cystic cancer", "adenoid cystic carcinoma of the pharynx", "Adenoid Cystic Carcinoma of the Pharynx", "Pharyngeal Throat Adenoid Cystic Cancer", "adenoid cystic carcinoma of pharynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pharyngeal adenoid cystic carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0014686", "names": ["SSMED", "SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION", "short stature, microcephaly, and endocrine dysfunction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short stature, microcephaly, and endocrine dysfunction", "shortest_name_length": 5}
{"curie": "MONDO:0004787", "names": ["Cervical Müllerian Papilloma", "cervical Mullerian papilloma", "cervical Müllerian papilloma", "Cervical Mullerian Papilloma", "cervical mullerian papilloma", "cervical Muellerian papilloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical mullerian papilloma", "shortest_name_length": 28}
{"curie": "MONDO:0010988", "names": ["aplasia cutis myopia", "Aplasia cutis-myopia syndrome", "aplasia cutis-myopia syndrome", "Gershoni Baruch Leibo syndrome", "Gershoni-Baruch-Leibo syndrome", "Aplasia cutis with myopia syndrome", "Aplasia cutis with myopia syndrome (disorder)", "APLASIA CUTIS CONGENITA, HIGH MYOPIA, AND CONE-ROD DYSFUNCTION", "Aplasia Cutis Congenita, High Myopia, and Cone-Rod Dysfunction", "aplasia cutis congenita, high myopia, and cone-rod dysfunction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aplasia cutis-myopia syndrome", "shortest_name_length": 20}
{"curie": "MONDO:0015454", "names": ["MCD", "Multiple Carboxylase Deficiency", "Combined Carboxylase Deficiency", "Multiple carboxylase deficiency", "multiple carboxylase deficiency", "Deficiency, Multiple Carboxylase", "Carboxylase Deficiency, Combined", "Deficiency, Combined Carboxylase", "Carboxylase Deficiency, Multiple", "Multiple Carboxylase Deficiencies", "Combined Carboxylase Deficiencies", "Deficiencies, Combined Carboxylase", "Deficiencies, Multiple Carboxylase", "Carboxylase Deficiencies, Multiple", "Carboxylase Deficiencies, Combined", "Multiple carboxylase deficiency (MCD)", "Multiple carboxylase deficiency (disorder)", "multiple carboxylase deficiency (diagnosis)", "Multiple carboxylase deficiency, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple carboxylase deficiency", "shortest_name_length": 3}
{"curie": "MONDO:0020841", "names": ["NEDCAS", "NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES", "neurodevelopmental disorder with cerebellar atrophy and with or without seizures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with cerebellar atrophy and with or without seizures", "shortest_name_length": 6}
{"curie": "MONDO:0000910", "names": ["RP6", "RP 6", "retinitis pigmentosa 6", "Retinitis Pigmentosa 6", "RETINITIS PIGMENTOSA 6", "retinitis pigmentosa type 6", "RETINITIS PIGMENTOSA 6 (disorder)", "Retinitis Pigmentosa, X-Linked Recessive, 6", "RETINITIS PIGMENTOSA, X-LINKED RECESSIVE, 6", "retinitis pigmentosa, X-linked recessive, 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 6", "shortest_name_length": 3}
{"curie": "MONDO:0008363", "names": ["RAINDROP HYPOPIGMENTATION", "raindrop hypopigmentation", "Raindrop Hypopigmentation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "raindrop hypopigmentation", "shortest_name_length": 25}
{"curie": "MONDO:0018695", "names": ["H5N1", "H7N9", "Bird flu", "Bird Flu", "bird flu", "Avian Flu", "Avian flu", "avian flu", "Flu, Avian", "Fowl plague", "Fowl Plague", "fowl plague", "Plague, Fowl", "bird flu virus", "Bird influenza", "avian flu virus", "Avian Influenza", "Avian influenza", "avian influenza", "Avian Influenzas", "Influenza, Avian", "Influenzas, Avian", "Influenza in Bird", "Influenza in Birds"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "avian influenza", "shortest_name_length": 4}
{"curie": "UMLS:C5669677", "names": ["Central Nervous System Myelomatosis", "Central Nervous System Plasma Cell Myeloma", "Extramedullary Disease in Multiple Myeloma Involving the Central Nervous System", "Extramedullary Disease in Plasma Cell Myeloma Involving the Central Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extramedullary Disease in Plasma Cell Myeloma Involving the Central Nervous System", "shortest_name_length": 35}
{"curie": "MONDO:0009782", "names": ["Ophthalmoplegia Totalis with Ptosis and Miosis", "ophthalmoplegia totalis with ptosis and miosis", "OPHTHALMOPLEGIA TOTALIS WITH PTOSIS AND MIOSIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ophthalmoplegia totalis with ptosis and miosis", "shortest_name_length": 46}
{"curie": "UMLS:C5420150", "names": ["Advanced Chordoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Chordoma", "shortest_name_length": 17}
{"curie": "UMLS:C4521745", "names": ["Stage III Esophageal Squamous Cell Cancer", "Pathologic Stage III Esophageal Squamous Cell Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage III Esophageal Squamous Cell Carcinoma AJCC v8", "shortest_name_length": 41}
{"curie": "MONDO:0001081", "names": ["cervicitis acute", "Acute cervicitis", "acute cervicitis", "Acute Cervicitis", "acute cervicitis (disease)", "Acute cervicitis (disorder)", "cervicitis (disease), acute", "Acute cervicitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute cervicitis", "shortest_name_length": 16}
{"curie": "UMLS:C4526965", "names": ["Stage I Gastric and Omental GIST AJCC v8", "Stage I Gastric and Omental Gastrointestinal Stromal Tumor AJCC v8", "Stage I Gastric (Stomach) and Omental Gastrointestinal Stromal Tumor (GIST)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Gastric and Omental Gastrointestinal Stromal Tumor AJCC v8", "shortest_name_length": 40}
{"curie": "MONDO:0017252", "names": ["CPAM type 4", "congenital pulmonary airway malformation type 4", "congenital cystic adenomatous malformation of the lung type 4", "congenital cystic adenomatoid malformation of the lung type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital pulmonary airway malformation type 4", "shortest_name_length": 11}
{"curie": "UMLS:C1336412", "names": ["Stage IV Ampullary Carcinoma", "Ampulla of Vater Cancer Stage IV", "Stage IV Ampulla of Vater Cancer", "Stage IV Ampulla of Vater Carcinoma", "Stage IV Ampulla of Vater Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Ampulla of Vater Cancer AJCC v7", "shortest_name_length": 28}
{"curie": "UMLS:C4331313", "names": ["Stage 0 Oropharyngeal (p16-Negative) Throat Cancer", "Stage 0 Oropharyngeal (p16-Negative) Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Oropharyngeal (p16-Negative) Carcinoma AJCC v8", "shortest_name_length": 50}
{"curie": "MONDO:0019454", "names": ["raeb", "RAEM", "RAEB", "MDS-EB", "RAEB NOS", "smoldering leukemia", "Smoldering Leukemia", "Smouldering leukemia", "Smouldering Leukemia", "Leukemia, Smoldering", "Smoldering Leukemias", "Leukemia, Smouldering", "Leukemias, Smoldering", "Smouldering leukaemia", "anemia refractory with excess blasts", "refractory anemia with excess blasts", "Refractory anemia with excess blasts", "refractory Anemia with Excess blasts", "Refractory Anemia with Excess Blasts", "Refractory anaemia with excess blasts", "Refractory Anemia with Excess of Blasts", "Refractory anemia with excess of blasts", "Refractory anaemia with excess of blasts", "Anemia, Refractory, with Excess of Blasts", "Refractory Anemia with an Excess of Blasts", "Refractory anemia with an excess of blasts", "refractory Anemia with an Excess of blasts", "[M] Refractory anemia with excess of blasts", "Myelodysplastic Syndrome with Excess Blasts", "Refractory anemia with excess blasts (RAEB)", "Myelodysplastic syndrome with excess blasts", "Refractory anaemia with an excess of blasts", "refractory anemia with excess blasts (RAEB)", "RAEB - Refractory anemia with excess blasts", "myelodysplastic syndrome with Excess blasts", "myelodysplastic syndrome with excess blasts", "[M] Refractory anaemia with excess of blasts", "RAEB - Refractory anaemia with excess blasts", "Refractory anemia with excess of blasts [RAEB]", "refractory anemia with excess blasts (diagnosis)", "refractory; anemia, with excess of blasts [RAEB]", "anemia; refractory, with excess of blasts [RAEB]", "Refractory anemia with excess of blasts, unspecified", "Myelodysplastic syndrome with excess blasts (disorder)", "Myelodysplastic syndrome with excess blasts (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myelodysplastic syndrome with excess blasts", "shortest_name_length": 4}
{"curie": "MONDO:0011776", "names": ["CAPS3", "IOMID", "CINCA", "NOMID", "CINCA/NOMID", "IOMID syndrome", "CINCA syndrome", "NOMID syndrome", "CINCA Syndrome", "IOMID Syndrome", "CINCA SYNDROME", "IOMID Syndromes", "Syndrome, IOMID", "Prieur-Griscelli Syndrome", "Prieur Griscelli Syndrome", "Prieur-Griscelli syndrome", "Prieur Griscelli syndrome", "Prieur-Griscelli Syndromes", "Syndrome, Prieur-Griscelli", "cryopyrin-associated periodic syndrome 3", "Cryopyrin-associated periodic syndrome 3", "CRYOPYRIN-ASSOCIATED PERIODIC SYNDROME 3", "Neonatal Onset Multisystem Inflammatory Disease", "neonatal-onset multisystem inflammatory disease", "Neonatal onset multisystem inflammatory disease", "Neonatal-Onset Multisystem Inflammatory Disease", "Neonatal-onset multisystem inflammatory disease", "neonatal onset multisystem inflammatory disease", "Infantile-onset multisystem inflammatory disease", "infantile onset multisystem inflammatory disease", "Infantile Onset Multisystem Inflammatory Disease", "Multisystem Inflammatory Disease, Neonatal Onset", "multisystem inflammatory disease, neonatal-onset", "infantile-onset multisystem inflammatory disease", "MULTISYSTEM INFLAMMATORY DISEASE, NEONATAL-ONSET", "Multisystem Inflammatory Disease, Neonatal-Onset", "Neonatal-onset multisystemic inflammatory disease", "chronic neurologic cutaneous and articular syndrome", "Chronic Neurologic Cutaneous and Articular Syndrome", "CHRONIC NEUROLOGIC CUTANEOUS AND ARTICULAR SYNDROME", "Chronic Neurologic, Cutaneous, and Articular Syndrome", "NOMID - Neonatal onset multisystem inflammatory disease", "neonatal-onset multisystem inflammatory disease (NOMID)", "chronic infantile neurological cutaneous articular syndrome", "chronic infantile neurological cutaneous and articular syndrome", "Chronic Infantile Neurologic, Cutaneous, and Articular Syndrome", "Chronic infantile neurological cutaneous and articular syndrome", "Chronic, Infantile, Neurological, Cutaneous, Articular Syndrome", "Chronic Infantile Neurological Cutaneous and Articular Syndrome", "Chronic infantile neurological, cutaneous and articular syndrome", "Chronic Infantile Neurological, Cutaneous, and Articular Syndrome", "neonatal-onset multisystem inflammatory disease (NOMID) (diagnosis)", "Chronic infantile neurological, cutaneous and articular syndrome [CINCA]", "CINCA - Chronic infantile neurological, cutaneous and articular syndrome", "Chronic infantile neurological, cutaneous and articular syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CINCA syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0020516", "names": ["Thymic Neuroendocrine Carcinoma", "thymic neuroendocrine carcinoma", "thymus neuroendocrine carcinoma", "Thymic neuroendocrine carcinoma", "neuroendocrine carcinoma of thymus", "Neuroendocrine carcinoma of thymus", "Neuroendocrine carcinoma of thymus (disorder)", "neuroendocrine carcinoma of thymus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thymic neuroendocrine carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0005671", "names": ["Blastocystis infection", "Blastocystis Infection", "Infection, Blastocystis", "infection, Blastocystis", "Blastocystis Infections", "Blastocystis infections", "Infections, Blastocystis", "infections, Blastocystis", "Blastocystis infectious disease", "Infection caused by Blastocystis", "Blastocystis hominis infectious disease", "Infection caused by Blastocystis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Blastocystis infectious disease", "shortest_name_length": 22}
{"curie": "UMLS:C5206813", "names": ["Locally Advanced Gastric Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Gastric Carcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0008325", "names": ["PSEUDOATROPHODERMA COLLI", "Pseudoatrophoderma colli", "Pseudoatrophoderma Colli", "Pseudoatrophoderma colli (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pseudoatrophoderma colli", "shortest_name_length": 24}
{"curie": "MONDO:0008900", "names": ["Camptodactyly, fibrous tissue hyperplasia, and skeletal dysplasia", "camptodactyly, fibrous tissue hyperplasia, and skeletal dysplasia", "CAMPTODACTYLY WITH FIBROUS TISSUE HYPERPLASIA AND SKELETAL DYSPLASIA", "camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia", "Camptodactyly with Fibrous Tissue Hyperplasia and Skeletal Dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia", "shortest_name_length": 65}
{"curie": "MONDO:0043073", "names": ["Zadik Barak Levin syndrome", "Zadik-Barak-Levin syndrome", "dermoid cysts, hypothyroidism, cleft palate and hypodontia", "Dermoid cysts, hypothyroidism, cleft palate, and hypodontia", "dermoid cysts, hypothyroidism, cleft palate, and hypodontia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Zadik-Barak-Levin syndrome", "shortest_name_length": 26}
{"curie": "UMLS:C4330471", "names": ["Iatrogenic Primary Hypothyroidism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Iatrogenic Primary Hypothyroidism", "shortest_name_length": 33}
{"curie": "MONDO:0022435", "names": ["Mauriac Syndrome", "Mauriac syndrome", "MAURIAC SYNDROME", "mauriac syndrome", "mauriac's syndrome", "Mauriac's syndrome", "Mauriac's syndrome (disorder)", "DIABETES-DWARFISM-OBESITY SYNDROME", "Dwarfism-hepatomegaly-obesity-juvenile diabetes syndrome", "dwarfism-hepatomegaly-obesity-juvenile diabetes syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mauriac syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0018743", "names": ["immune-mediated acquired neuromuscular junction disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immune-mediated acquired neuromuscular junction disease", "shortest_name_length": 55}
{"curie": "UMLS:C1275252", "names": ["Spindle Cell Type Atypical Fibroxanthoma", "Atypical fibroxanthoma - spindle cell type", "Atypical fibroxanthoma - spindle cell type (disorder)", "Atypical fibroxanthoma - spindle cell type (diagnosis)", "skin neoplasm malignant fibrohistiocytic atypical fibroxanthoma spindle cell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypical fibroxanthoma - spindle cell type", "shortest_name_length": 40}
{"curie": "MONDO:0030356", "names": ["SRTD21", "short-rib thoracic dysplasia 21 without polydactyly", "SHORT-RIB THORACIC DYSPLASIA 21 WITHOUT POLYDACTYLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short-rib thoracic dysplasia 21 without polydactyly", "shortest_name_length": 6}
{"curie": "UMLS:C5420396", "names": ["Primary Bone Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Bone Diffuse Large B-Cell Lymphoma", "shortest_name_length": 42}
{"curie": "MONDO:0001803", "names": ["MYRINGITIS BULLOUS", "myringitis bullosa", "bullous myringitis", "Myringitis bullosa", "Bullous myringitis", "Myringitis bullous", "Bullous Myringitis", "myringitis bullous", "BULLOUS MYRINGITIS", "myringitis; bullous", "bullous; myringitis", "Bullous myringitis (disorder)", "myringitis bullous (diagnosis)", "Myringitis bullosa hemorrhagica", "myringitis bullosa hemorrhagica", "Myringitis bullosa haemorrhagica"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myringitis bullosa hemorrhagica", "shortest_name_length": 18}
{"curie": "MONDO:0022208", "names": ["Crystal arthritis", "Crystal Arthritis", "crystal arthritis", "Arthritis, Crystal", "arthritis; crystals", "Arthropathy;crystal", "crystals; arthritis", "crystal arthropathy", "Crystal arthropathy", "Crystal Arthritides", "Crystal Arthropathy", "Arthropathy, Crystal", "Arthritides, Crystal", "Crystal arthropathies", "crystalline arthritis", "Crystalline arthritis", "crystal arthropathies", "arthropathy; crystals", "Crystalline Arthritis", "Crystal Arthropathies", "crystals; arthropathy", "Arthropathies, Crystal", "Arthritis, Crystalline", "ARTHROPATHY CRYSTALLINE", "Crystalline Arthritides", "Crystalline Arthropathy", "Arthropathy crystal NOS", "crystalline arthropathy", "Arthropathy, Crystalline", "Crystal arthropathy, NOS", "Arthritides, Crystalline", "Crystalline Arthropathies", "Crystalline arthritis, NOS", "Arthropathies, Crystalline", "Crystal arthropathy (disorder)", "Unspecified crystal arthropathy", "Crystal arthropathy, unspecified", "crystalline arthropathy (diagnosis)", "Crystal-induced arthritis AND/OR synovitis", "crystal-induced arthritis and/or synovitis", "Crystal-induced arthritis and synovitis, NOS", "Crystal-related arthropathy and periarthropathy", "crystal-related arthropathy and periarthropathy", "Unspecified crystal arthropathy, site unspecified", "Crystal arthropathy, unspecified, site unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "crystal arthropathy", "shortest_name_length": 17}
{"curie": "MONDO:0017114", "names": ["global cerebellar malformation", "diffuse cerebellar malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "global cerebellar malformation", "shortest_name_length": 30}
{"curie": "MONDO:0001868", "names": ["Narrow angle glaucoma", "Closed-angle glaucoma", "Angle closure glaucoma", "ACG - Angle-closure glaucoma", "primary Angle Closure Glaucoma", "primary angle-closure glaucoma", "Primary angle closure glaucoma", "Primary angle-closure glaucoma", "primary angle closure glaucoma", "Glaucoma, angle-closure, primary", "Primary angle-closure glaucoma, NOS", "Primary angle-closure glaucoma (disorder)", "primary angle-closure glaucoma (diagnosis)", "Unspecified primary angle-closure glaucoma", "Primary angle-closure glaucoma, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary angle-closure glaucoma", "shortest_name_length": 21}
{"curie": "MONDO:0015614", "names": ["Duhring", "DUHRING DISEASE", "duhring disease", "Duhring Disease", "Disease, Duhring", "Duhrings Disease", "duhrings disease", "Duhring's disease", "disease duhring's", "duhring's disease", "Duhring's Disease", "Disease, Duhring's", "Durhing-Brocq disease", "Duhring-Brocq disease", "Dermatitis herpetiformis", "Dermatitis Herpetiformis", "Dermatitis;herpetiformis", "Dermatosis herpetiformis", "herpetiformis dermatitis", "DERMATITIS HERPETIFORMIS", "dermatitis herpetiformis", "dermatosis herpetiformis", "herpetiformis; dermatitis", "DERMATITIS, HERPETIFORMIS", "herpetiformis; dermatosis", "dermatosis; herpetiformis", "dermatitis; herpetiformis", "DH - Dermatitis herpetiformis", "Dermatitis herpetiformis (disorder)", "dermatitis herpetiformis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermatitis herpetiformis", "shortest_name_length": 7}
{"curie": "MONDO:0021392", "names": ["colorectal polyp", "Polyp colorectal", "Colorectal Polyp", "large bowel polyp", "Colorectal polyps", "Large Bowel Polyp", "colorectal polyps", "Colorectal polyposis", "polyp of large bowel", "Polyp of Large Bowel", "Large Intestine Polyp", "Large intestine polyp", "large intestine polyp", "polyp of the large bowel", "polyp of large intestine", "Polyp of Large Intestine", "Polyp of the Large Bowel", "Polyp of large intestine", "polyp of the large intestine", "Polyp of the Large Intestine", "Polyp of large intestine (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyp of large intestine", "shortest_name_length": 16}
{"curie": "MONDO:0001184", "names": ["chronic rapidly progressive glomerulonephritis", "rapidly progressive glomerulonephritis, chronic", "chronic rapidly progressive glomerulonephritis (diagnosis)", "Chronic glomerulonephritis with lesion of rapidly progressive glomerulonephritis", "chronic glomerulonephritis with lesion of rapidly progressive glomerulonephritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic rapidly progressive glomerulonephritis", "shortest_name_length": 46}
{"curie": "MONDO:0002247", "names": ["Stuart", "F10 DEFICIENCY", "Factor X deficiency", "factor x deficiency", "FACTOR X DEFICIENCY", "Factor X Deficiency", "factor X deficiency", "Deficiency, Factor X", "Factor 10 deficiency", "Factor 10 Deficiency", "Deficiency, factor X", "Deficiency, Factor 10", "Factor Ten Deficiency", "Factor X Deficiencies", "Deficiency, Factor Ten", "Factor 10 Deficiencies", "Disease, Stuart-Prower", "Deficiencies, Factor X", "Factor Ten Deficiencies", "Deficiencies, Factor 10", "Deficiencies, Factor Ten", "Factor X deficiency, NOS", "Stuart-Prower Deficiency", "Ten Deficiencies, Factor", "Stuart Prower Deficiency", "Stuart-Prower; deficiency", "Deficiency, Stuart Prower", "Deficiency, Stuart-Prower", "deficiency; Stuart-Prower", "Reduced factor X activity", "Decreased factor x activity", "Congenital factor X deficiency", "Factor X deficiency (disorder)", "Stuart Prower Factor Deficiency", "STUART-PROWER FACTOR DEFICIENCY", "Stuart-Prower factor deficiency", "Stuart-Prower Factor Deficiency", "Deficiency, Stuart-Prower Factor", "Deficiency, Stuart Prower Factor", "Congenital Stuart factor deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "factor X deficiency", "shortest_name_length": 6}
{"curie": "UMLS:C2825032", "names": ["Withdrawn", "Withdrawal", "Withdrawal (dysfunction)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Withdrawal (dysfunction)", "shortest_name_length": 9}
{"curie": "OMIM:612671", "names": ["GOUT4", "UAQTL4", "GOUT SUSCEPTIBILITY 4", "URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 5}
{"curie": "MONDO:0004222", "names": ["Ovarian Clear Cell Cystadenocarcinoma", "ovarian clear cell cystadenocarcinoma", "ovarian mesonephroid cystadenocarcinoma", "cystadenocarcinoma, clear cell, ovarian", "mesonephroid cystadenocarcinoma, ovarian", "cystadenocarcinoma, mesonephroid, ovarian", "clear cell cystadenocarcinoma of the ovary", "ovary cancer, clear cell cystadenocarcinoma", "cystadenocarcinoma of the ovary, clear cell", "ovarian cancer, clear cell cystadenocarcinoma", "ovary cancer, mesonephroid cystadenocarcinoma", "ovarian cancer, mesonephroid cystadenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian clear cell cystadenocarcinoma", "shortest_name_length": 37}
{"curie": "UMLS:C5205916", "names": ["Advanced Clear Cell Sarcoma of Soft Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Clear Cell Sarcoma of Soft Tissue", "shortest_name_length": 42}
{"curie": "MONDO:0008788", "names": ["IRIDA", "IRIDA syndrome", "pseudo-iron-deficiency Anemia", "iron-handling disorder, hereditary", "Iron-Refractory Iron Deficiency Anemia", "iron-refractory iron deficiency anemia", "anemia, hypochromic microcytic, with defect in iron metabolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IRIDA syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C1740834", "names": ["Recurrent EBV Infection", "Recurrent Epstein-Barr Virus Infection", "Epstein-Barr virus infection recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epstein-Barr virus infection recurrent", "shortest_name_length": 23}
{"curie": "MONDO:0012669", "names": ["NFLS", "LGSS", "Legius Syndrome", "Legius syndrome", "LEGIUS SYNDROME", "NF1-like syndrome", "Legius syndrome (diagnosis)", "neurofibromatosis 1-like syndrome", "Neurofibromatosis 1-like syndrome", "Neurofibromatosis Type 1-Like Syndrome", "Neurofibromatosis Type 1-like Syndrome", "neurofibromatosis type 1-like syndrome", "neurofibromatosis type 1 like syndrome", "NEUROFIBROMATOSIS TYPE 1-LIKE SYNDROME", "Neurofibromatosis type 1-like syndrome", "NEUROFIBROMATOSIS, TYPE 1-LIKE SYNDROME", "NFLS - neurofibromatosis type 1-like syndrome", "Neurofibromatosis type 1-like syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Legius syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C5556797", "names": ["Refractory Cervical Squamous Cell Carcinoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Cervical Squamous Cell Carcinoma, Not Otherwise Specified", "shortest_name_length": 68}
{"curie": "UMLS:C2111748", "names": ["Salivary Gland Large Cell Neuroendocrine Carcinoma", "large cell neuroendocrine carcinoma of salivary gland", "large cell neuroendocrine carcinoma of salivary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "large cell neuroendocrine carcinoma of salivary gland", "shortest_name_length": 50}
{"curie": "MONDO:0006321", "names": ["adrenal cortical incidentaloma", "Adrenal Cortical Incidentaloma", "Nonfunctional Adrenal Cortex Adenoma", "nonfunctional adrenal cortex adenoma", "Non-Functioning Adrenal Gland Adenoma", "Nonfunctioning Adrenal Cortex Adenoma", "Non-Functioning Adrenal Cortex Adenoma", "non-functioning adrenal cortex adenoma", "non-functioning adrenal cortical adenoma", "Non-Functioning Adrenal Cortical Adenoma", "adrenal cortex non-functioning endocrine neoplasm", "non-functioning endocrine neoplasm of adrenal cortex"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-functioning adrenal cortex adenoma", "shortest_name_length": 30}
{"curie": "UMLS:C5418575", "names": ["Skin ALT/WDLPS", "Skin Atypical Lipomatous Tumor", "Skin Atypical Lipomatous Tumor/Well Differentiated Liposarcoma", "Skin Atypical Lipomatous Tumor/Well-Differentiated Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin Atypical Lipomatous Tumor/Well Differentiated Liposarcoma", "shortest_name_length": 14}
{"curie": "MONDO:0001218", "names": ["acute laryngopharyngitis", "laryngopharyngitis acute", "Acute laryngopharyngitis", "Acute laryngopharyngitis (disorder)", "acute laryngopharyngitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute laryngopharyngitis", "shortest_name_length": 24}
{"curie": "MONDO:0007486", "names": ["HBID", "Dkbi", "DKBI", "Witkop-Von Sallmann disease", "Witkop-Von Sallmann Disease", "Witkop-von Sallman syndrome", "Hereditary benign intraepithelial dyskeratosis", "Hereditary Benign Intraepithelial Dyskeratosis", "hereditary benign intraepithelial dyskeratosis", "Dyskeratosis, Hereditary Benign Intraepithelial", "dyskeratosis, hereditary benign intraepithelial", "DYSKERATOSIS, HEREDITARY BENIGN INTRAEPITHELIAL", "hereditary benign corneal intraepithelial dyskeratosis", "Hereditary benign corneal intraepithelial dyskeratosis", "Hereditary benign intraepithelial dyskeratosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary benign intraepithelial dyskeratosis", "shortest_name_length": 4}
{"curie": "UMLS:C1332496", "names": ["Benign Extragonadal Germ Cell Tumor", "Benign Extragonadal Germ Cell Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Extragonadal Germ Cell Tumor", "shortest_name_length": 35}
{"curie": "MONDO:0000667", "names": ["auditory agnosia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "auditory agnosia", "shortest_name_length": 16}
{"curie": "UMLS:C3899975", "names": ["BCLC Stage D Hepatocellular Cancer", "BCLC Stage D Hepatocellular Carcinoma", "Barcelona Clinic Liver Cancer Stage D Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "BCLC Stage D Hepatocellular Carcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0023069", "names": ["enlarged vestibular aqueduct", "large vestibular aqueduct syndrome", "enlarged vestibular aqueduct syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "enlarged vestibular aqueduct syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0030004", "names": ["AUTS20", "autism, susceptibility to, 20", "AUTISM, SUSCEPTIBILITY TO, 20"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autism, susceptibility to, 20", "shortest_name_length": 6}
{"curie": "UMLS:C0520560", "names": ["Hemorrhagic esophagitis", "Esophagitis hemorrhagic", "Haemorrhagic oesophagitis", "Oesophagitis haemorrhagic", "Hemorrhagic esophagitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemorrhagic esophagitis", "shortest_name_length": 23}
{"curie": "UMLS:C4761226", "names": ["Advanced gastric carcinoma", "Advanced Gastric Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced gastric carcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0004948", "names": ["cll", "SLL", "CLL", "BCLL", "clls", "B-CLL", "B Cell CLL", "b-cell cll", "B-Cell CLL", "B-cell CLL", "B cell CLL", "CLL, B-cell", "SL lymphoma", "DLWD lymphoma", "DWDL lymphoma", "b-cell leukemia", "b cell leukemia", "leukemia b cell", "Small Cell Lymphoma", "Small cell lymphoma", "Small-Cell Lymphoma", "Lymphoma, Small-Cell", "Lymphocytic lymphoma", "Small-Cell Lymphomas", "diffuse WDL lymphoma", "Lymphocytic Lymphoma", "Lymphoma, Small Cell", "lymphocytic lymphoma", "Lymphocytic Lymphomas", "Lymphomas, Small-Cell", "Lymphoma, Lymphocytic", "Lymphomas, Lymphocytic", "Chronic B-Cell Leukemia", "Leukemia, Chronic B-Cell", "B-Cell Leukemia, Chronic", "Chronic B-Cell Leukemias", "B Cell Leukemia, Chronic", "WDL, diffuse lymphocytic", "Leukemia, B Cell, Chronic", "B-Cell Leukemias, Chronic", "chronic lymphoid leukemia", "Lymphocytic lymphosarcoma", "Leukemia, B-Cell, Chronic", "Chronic lymphoid leukemia", "Leukemias, Chronic B-Cell", "Chronic lymphatic leukemia", "Small lymphocytic lymphoma", "Chronic lymphoid leukaemia", "Small Lymphocytic Lymphoma", "small lymphocytic lymphoma", "lymphoplasmacytic leukemia", "Chronic Lymphatic Leukemia", "chronic lymphatic leukemia", "Lymphoid leukemia, chronic", "lymphoma small lymphocytic", "Lymphocytic Lymphoma, Small", "Low-Grade B-Cell Malignancy", "B Cell Lymphocytic Leukemia", "Lymphoma, Small Lymphocytic", "B-cell lymphocytic leukemia", "lymphoplasmacytic leukaemia", "leukemia, chronic lymphatic", "chronic lymphatic leukaemia", "Lymphatic Leukemia, Chronic", "B cell lymphocytic leukemia", "Small Lymphocytic Lymphomas", "Chronic lymphatic leukaemia", "Lymphoid leukaemia, chronic", "Chronic Lymphatic Leukemias", "LEUKEMIA, CHRONIC LYMPHATIC", "Leukemia, Chronic Lymphatic", "lymphocytic lymphoma, small", "B-Cell Lymphocytic Leukemia", "lymphoma, small lymphocytic", "b cell lymphocytic leukemia", "Chronic Lymphocytic Leukemia", "[M]Chronic lymphoid leukemia", "chronic leukemia lymphocytic", "chronic lymphocytic leukemia", "lymphatic; leukemia, chronic", "Malignancy, Low-Grade B-Cell", "lymphocytic leukemia chronic", "CHRONIC LYMPHOCYTIC LEUKEMIA", "Leukemia lymphocytic chronic", "B-Cell Malignancy, Low-Grade", "Chronic lymphocytic leukemia", "B Cell Malignancy, Low Grade", "leukemia chronic lymphocytic", "Lymphatic Leukemias, Chronic", "leukemia; lymphatic, chronic", "Lymphomas, Small Lymphocytic", "LEUKEMIA CHRONIC LYMPHOCYTIC", "Lymphocytic Lymphomas, Small", "LEUKEMIA LYMPHOCYTIC CHRONIC", "diffuse lymphocytic lymphoma", "Leukemias, Chronic Lymphatic", "Diffuse lymphocytic lymphoma", "leukemia, chronic lymphocytic", "Leukemias chronic lymphocytic", "chronic lymphocytic leukaemia", "[M]Chronic lymphoid leukaemia", "Lymphocytic lymphoma, diffuse", "Leukemia, Chronic Lymphocytic", "leukemia, chronic LYMPHOCYTIC", "Lymphocytic Leukemia, Chronic", "LEUKEMIA, CHRONIC LYMPHOCYTIC", "Leukaemia;chronic lymphocytic", "Low-Grade B-Cell Malignancies", "lymphoma; diffuse, small cell", "Leukaemia lymphocytic chronic", "diffuse; lymphoma, small cell", "chronic lymphogenous leukemia", "Chronic lymphocytic leukaemia", "lymphocytic leukemia, chronic", "Chronic Lymphocytic Leukemias", "LEUKEMIA, LYMPHOCYTIC, CHRONIC", "Malignant lymphoma, small cell", "Leukemia, Lymphocytic, Chronic", "B-Cell Malignancies, Low-Grade", "Chronic Lymphoblastic Leukemia", "Lymphocytic Leukemias, Chronic", "b chronic lymphocytic leukemia", "Disrupted In B-Cell Malignancy", "chronic lymphoblastic leukemia", "Disrupted In B Cell Malignancy", "leukemia, lymphocytic, chronic", "Malignancies, Low-Grade B-Cell", "Leukaemias chronic lymphocytic", "Chronic B-Lymphocytic Leukemia", "Leukemia, Chronic B-Lymphocytic", "Lymphoblastic Leukemia, Chronic", "B Lymphocytic Leukemia, Chronic", "B-Lymphocytic Leukemia, Chronic", "Malignant lymphoma - small cell", "Chronic Lymphoblastic Leukemias", "Chronic B-Lymphocytic Leukemias", "Small cell lymphocytic lymphoma", "CLL Lymphoplasmacytoid Lymphoma", "Small lymphocytic lymphoma, NOS", "cll chronic lymphocytic leukemia", "Lymphoma, Lymphocytic, Malignant", "Leukemias, Chronic B-Lymphocytic", "Leukemias, Chronic Lymphoblastic", "B-cell chronic lymphoid leukemia", "CLL Lymphoplasmacytoid Lymphomas", "Chronic lymphocytic leukemia NOS", "B-Cell Chronic Lymphoid Leukemia", "Lymphoblastic Leukemias, Chronic", "B-Lymphocytic Leukemias, Chronic", "Leukemia, Lymphoblastic, Chronic", "Lymphoplasmacytoid Lymphoma, CLL", "Lymphoma, CLL Lymphoplasmacytoid", "Lymphomas, CLL Lymphoplasmacytoid", "Diffuse lymphocytic lymphosarcoma", "Chronic lymphocytic leukaemia NOS", "Small B-Cell Lymphocytic Lymphoma", "Lymphoplasmacytoid Lymphomas, CLL", "Lymphoma, Lymphoplasmacytoid, CLL", "small B-cell lymphocytic lymphoma", "lymphocytic; lymphoma, small cell", "B-Cell Small Lymphocytic Lymphoma", "lymphoma; lymphocytic, small cell", "Chronic lymphocytic leukemia, NOS", "B-cell small lymphocytic lymphoma", "chronic lymphocytic leukemia (cll)", "Lymphocytic lymphosarcoma, diffuse", "chronic lymphocytic leukemia (CLL)", "B-cell small lymphocytic lymphomas", "CLL (chronic lymphocytic leukemia)", "Chronic lymphoid leukemia, disease", "Chronic Lymphocytic Leukemia (CLL)", "leukemia lymphocytic chronic (CLL)", "CLL - Chronic lymphocytic leukemia", "Chronic B-Cell Lymphocytic Leukemia", "B cell chronic lymphocytic leukemia", "chronic B-cell lymphocytic leukemia", "B-cell chronic lymphocytic leukemia", "Chronic lymphoid leukaemia, disease", "B-Cell Chronic Lymphocytic Leukemia", "B Cell Chronic Lymphocytic Leukemia", "CLL - Chronic lymphocytic leukaemia", "Leukemia, chronic lymphocytic (CLL)", "Malignant lymphoma, small cell, NOS", "lymphocytic leukemia, B-cell chronic", "B-cell chronic lymphogenous leukemia", "chronic lymphocytic leukemia, B-cell", "leukemia, B-cell chronic lymphocytic", "B-cell chronic lymphocytic leukaemia", "Malignant lymphoma, lymphocytic, NOS", "Lymphocytic Leukemia, Chronic, B Cell", "B-cell small lymphocytic lymphoma NOS", "Malignant lymphoma, small lymphocytic", "Leukemia, Chronic Lymphocytic, B-Cell", "Lymphocytic Leukemia, Chronic, B-Cell", "Diffuse lymphocytic malignant lymphoma", "Malignant lymphoma - small lymphocytic", "LYMPHOMA, SMALL LYMPHOCYTIC, MALIGNANT", "Malignant lymphoma, small cell diffuse", "Leukemia, Lymphocytic, Chronic, B Cell", "Leukemia, Lymphocytic, Chronic, B-Cell", "Malignant lymphoma, small B lymphocytic", "well-differentiated lymphocytic lymphoma", "chronic lymphocytic leukemia (diagnosis)", "Well-Differentiated Lymphocytic Lymphoma", "Malignant lymphoma, lymphocytic, diffuse", "Chronic lymphocytic leukemia, B-cell type", "Lymphoma, Small Lymphocytic, Plasmacytoid", "Lymphocytic Lymphoma, Well-Differentiated", "Malignant lymphoma, small lymphocytic NOS", "Well-Differentiated Lymphocytic Lymphomas", "Lymphocytic Lymphoma, Well Differentiated", "Lymphoma, Well-Differentiated Lymphocytic", "Malignant lymphoma, lymphocytic cell type", "Malignant lymphoma, small lymphocytic, NOS", "Lymphoma, Lymphocytic, Well Differentiated", "Chronic lymphocytic leukaemia, B-cell type", "Lymphoma, Lymphocytic, Well-Differentiated", "Lymphomas, Well-Differentiated Lymphocytic", "Lymphocytic Lymphomas, Well-Differentiated", "Chronic lymphocytic leukemia of B-cell type", "diffuse well differentiated lymphoma (DLWD)", "B-CLL - B-cell chronic lymphocytic leukemia", "Malignant lymphoma, small cell, diffuse, NOS", "B-CLL - B-cell chronic lymphocytic leukaemia", "small B-cell lymphocytic lymphoma (diagnosis)", "Malignant lymphoma, lymphocytic, diffuse, NOS", "Chronic lymphoid leukemia, disease (disorder)", "Malignant lymphoma, small lymphocytic, diffuse", "Chronic lymphocytic leukemia of B-cell type NOS", "B-cell chronic lymphocytic leukemia (diagnosis)", "Diffuse Well Differentiated Lymphocytic Lymphoma", "Diffuse Well-Differentiated Lymphocytic Lymphoma", "diffuse well-differentiated lymphocytic lymphoma", "well-differentiated lymphoma, diffuse lymphocytic", "Malignant lymphoma - small lymphocytic (disorder)", "diffuse lymphocytic, well-differentiated lymphoma", "lymphoma, diffuse lymphocytic, well-differentiated", "Lymphocytic Lymphoma, Diffuse, Well-Differentiated", "hematopoeitic - chronic lymphocytic leukemia (CLL)", "Hematopoeitic - Chronic Lymphocytic Leukemia (CLL)", "Lymphocytic Lymphoma, Diffuse, Well Differentiated", "Lymphoma, Lymphocytic, Diffuse, Well-Differentiated", "Lymphoma, Lymphocytic, Diffuse, Well Differentiated", "Malignant lymphoma, lymphocytic, well differentiated", "lymphoma; diffuse, lymphocytic (well differentiated)", "diffuse; lymphoma, lymphocytic (well differentiated)", "diffuse well differentiated lymphoma (DLWD) (diagnosis)", "Malignant lymphoma lymphocytic well differentiated diffuse", "Small lymphocyte B lymphoma (Lukes-Collins Classification)", "Malignant lymphoma, lymphocytic, well differentiated, diffuse", "B-cell chronic lymphocytic leukemia/small lymphocytic lymphoma", "Malignant lymphoma, small lymphocytic (morphologic abnormality)", "B-cell chronic lymphocytic leukaemia/small lymphocytic lymphoma", "B-cell CLL/SLL (chronic lymphocytic leukemia/small lymphocytic lymphoma)", "B-cell CLL/SLL (chronic lymphocytic leukaemia/small lymphocytic lymphoma)", "B-cell chronic lymphocytic leukemia/small lymphocytic lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-cell chronic lymphocytic leukemia", "shortest_name_length": 3}
{"curie": "UMLS:C4520744", "names": ["stage I lip and oral cavity cancer", "Stage I Lip and Oral Cavity Cancer", "Lip and Oral Cavity Cancer Stage I", "Lip and Oral Cavity Carcinoma Stage I", "Stage I Lip and Oral Cavity Carcinoma", "Stage I Lip and Oral Cavity Cancer AJCC v7", "Stage I Lip and Oral Cavity Cancer AJCC v6", "Stage I Lip and Oral Cavity Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Lip and Oral Cavity Cancer AJCC v6 and v7", "shortest_name_length": 34}
{"curie": "UMLS:C4724967", "names": ["Refractory Synovial Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Synovial Sarcoma", "shortest_name_length": 27}
{"curie": "MONDO:0014987", "names": ["FANCU", "XRCC2 Fanconi anemia", "Fanconi anemia complementation group U", "FANCONI ANEMIA, COMPLEMENTATION GROUP U", "Fanconi anemia, complementation GROUP U", "Fanconi Anemia, complementation group U", "Fanconi anemia caused by mutation in XRCC2", "Fanconi anemia complementation group type U", "Fanconi Anemia, complementation group type U"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fanconi anemia complementation group U", "shortest_name_length": 5}
{"curie": "MONDO:0019278", "names": ["hair anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hair anomaly", "shortest_name_length": 12}
{"curie": "OMIM:120080", "names": ["CLCS", "COLCHICINE RESISTANCE", "COLCHICINE SENSITIVITY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 4}
{"curie": "UMLS:C5418907", "names": ["Resectable Adenocarcinoma of Unknown Primary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Adenocarcinoma of Unknown Primary", "shortest_name_length": 44}
{"curie": "UMLS:C4288080", "names": ["UNC13D Deficiency", "MUNC13-4 Deficiency", "MUNC13-4 Deficiency/UNC13D"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "UNC13D Deficiency", "shortest_name_length": 17}
{"curie": "MONDO:0017220", "names": ["LTEC0", "laryngotracheoesophageal cleft type 0", "laryngo-tracheo-esophageal cleft type 0"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laryngotracheoesophageal cleft type 0", "shortest_name_length": 5}
{"curie": "UMLS:C5420864", "names": ["Metastatic Thyroid Gland Oncocytic Carcinoma", "Metastatic Thyroid Gland Hurthle Cell Carcinoma", "Metastatic Thyroid Gland Oncocytic (Hurthle Cell) Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Thyroid Gland Oncocytic Carcinoma", "shortest_name_length": 44}
{"curie": "MONDO:0008870", "names": ["Bird headed dwarfism Montreal type", "Bird-headed dwarfism Montreal type", "bird headed-dwarfism, Montreal type", "Bird-Headed Dwarfism, Montreal Type", "Bird-headed dwarfism, Montreal type", "BIRD-HEADED DWARFISM, MONTREAL TYPE", "Microcephalic primordial dwarfism Montreal type", "microcephaly primordial dwarfism, Montreal type", "MICROCEPHALIC PRIMORDIAL DWARFISM, MONTREAL TYPE", "Microcephalic primordial dwarfism, Montreal type", "microcephalic primordial dwarfism, Montreal type", "Bird-headed dwarfism with features of premature senility", "Microcephalic primordial dwarfism Montreal type (disorder)", "microcephaly primordial dwarfism, Montreal type (diagnosis)", "premature senility, premature graying and loss of scalp hair and wrinkled skin of the palms"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bird headed-dwarfism, Montreal type", "shortest_name_length": 34}
{"curie": "MONDO:0014265", "names": ["AD18", "ALZHEIMER DISEASE 18", "Alzheimer disease 18", "Alzheimer's disease 18", "ADAM10 Alzheimer disease", "Alzheimer disease type 18", "Alzheimer's disease type 18", "ALZHEIMER DISEASE 18, LATE-ONSET", "Alzheimer disease 18, late-onset", "Alzheimer's disease 18, late onset", "Alzheimer disease 18, susceptibility to", "Alzheimer disease caused by mutation in ADAM10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alzheimer disease 18", "shortest_name_length": 4}
{"curie": "MONDO:0000152", "names": ["thiamine-responsive dysfunction syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thiamine-responsive dysfunction syndrome", "shortest_name_length": 40}
{"curie": "MONDO:0018101", "names": ["Familial primary hypomagnesemia with normocalciuria and normocalcemia", "familial primary hypomagnesemia with normocalciuria and normocalcemia", "Familial primary hypomagnesaemia with normocalciuria and normocalcemia", "FPHNN - familial primary hypomagnesemia with normocalciuria and normocalcemia", "FPHNN - familial primary hypomagnesaemia with normocalciuria and normocalcemia", "Familial primary hypomagnesemia with normocalciuria and normocalcemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial primary hypomagnesemia with normocalciuria and normocalcemia", "shortest_name_length": 69}
{"curie": "MONDO:0043094", "names": ["ichthyosis follicular", "Follicular ichthyosis", "follicular ichthyosis", "ichthyosis, follicular", "Follicular ichthyosis (disorder)", "Follicular ichthyosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ichthyosis, follicular", "shortest_name_length": 21}
{"curie": "UMLS:C3272795", "names": ["Colorectal FSA", "Colorectal Filiform Serrated Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Filiform Serrated Adenoma", "shortest_name_length": 14}
{"curie": "UMLS:C0854815", "names": ["Stage II Lymphoplasmacytic Lymphoma", "Ann Arbor Stage II Lymphoplasmacytic Lymphoma", "Lymphoplasmacytoid lymphoma/immunocytoma stage II", "Stage II Lymphoplasmacytoid Lymphoma/Immunocytoma", "Lymphoplasmacytoid Lymphoma/Immunocytoma Stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoplasmacytoid lymphoma/immunocytoma stage II", "shortest_name_length": 35}
{"curie": "MONDO:0000336", "names": ["meningovascular neurosyphilis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "meningovascular neurosyphilis", "shortest_name_length": 29}
{"curie": "MONDO:0006444", "names": ["TMT", "Somatic Malignancy", "Dermoid cyst with secondary tumor", "Dermoid cyst with secondary tumour", "teratoma with somatic-type malignancy", "Teratoma with Somatic-Type Malignancy", "Teratoma with malignant transformation", "Teratoma with Malignant Transformation", "teratoma with malignant transformation", "malignant; transformation dermoid cyst", "Dermoid Cyst with Malignant Transformation", "dermoid cyst with malignant transformation", "Dermoid cyst with malignant transformation", "dermoid; cyst, with malignant transformation", "teratoma with malignant transformation (diagnosis)", "Teratoma with malignant transformation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "teratoma with malignant transformation", "shortest_name_length": 3}
{"curie": "UMLS:C1963717", "names": ["Sleep-related eating disorder", "Sleep Related Eating Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sleep-related eating disorder", "shortest_name_length": 29}
{"curie": "MONDO:0015731", "names": ["high anorectal malformation", "High anorectal malformation", "High anorectal malformation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "high anorectal malformation", "shortest_name_length": 27}
{"curie": "UMLS:C0745153", "names": ["Hypoglycemic attack", "HYPOGLYCEMIC EPISODE", "Hypoglycaemic attack", "Hypoglycemic episode", "Hypoglycaemic episode", "Hypoglycemic episodes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypoglycaemic episode", "shortest_name_length": 19}
{"curie": "MONDO:0007893", "names": ["LEOPARD Syndrome", "leopard syndrome", "Leopard syndrome", "LEOPARD syndrome", "LEOPARD Syndromes", "Moynahan syndrome", "Syndrome, LEOPARD", "Gorlin syndrome II", "Syndromes, LEOPARD", "Generalized lentiginosis", "Generalised lentiginosis", "generalized lentiginosis", "Cardio-Cutaneous Syndrome", "Cardio Cutaneous Syndrome", "Syndrome, Cardio-Cutaneous", "Cardio-Cutaneous Syndromes", "Syndromes, Cardio-Cutaneous", "Multiple lentigines syndrome", "MULTIPLE LENTIGINES SYNDROME", "Cardiomyopathic Lentiginoses", "Lentiginosis Cardiomyopathic", "Multiple Lentigines Syndrome", "Cardiomyopathic lentiginosis", "Cardiomyopathic Lentiginosis", "multiple lentigines syndrome", "Cardiomyopathic, Lentiginosis", "Leopard syndrome lentiginosis", "Lentiginosis, Cardiomyopathic", "LENTIGINOSIS, CARDIOMYOPATHIC", "Lentiginoses, Cardiomyopathic", "Syndrome, Multiple Lentigines", "Lentigines Syndrome, Multiple", "Lentiginosis profusa syndrome", "Multiple Lentigines Syndromes", "Lentiginosis Cardiomyopathics", "lentiginosis profusa syndrome", "Cardiomyopathics, Lentiginosis", "Lentigines Syndromes, Multiple", "Syndromes, Multiple Lentigines", "Familial multiple lentigines syndrome", "familial multiple lentigines syndrome", "Multiple lentigines syndrome (disorder)", "Noonan syndrome with multiple lentigines", "Progressive cardiomyopathic lentiginosis", "Noonan Syndrome with Multiple Lentigines", "multiple lentigines syndrome (diagnosis)", "progressive cardiomyopathic lentiginosis", "Progressive Cardiomyopathic Lentiginosis", "Progressive Cardiomyopathic Lentiginoses", "Lentiginoses, Progressive Cardiomyopathic", "Cardiomyopathic Lentiginosis, Progressive", "Cardiomyopathic Lentiginoses, Progressive", "Lentiginosis, Progressive Cardiomyopathic", "Capute-Rimoin-Konigsmark-Esterly-Richardson syndrome", "lentigines, electrocardiographic conduction abnormalities, ocular hypertelorism, pulmonic stenosis, abnormal genitalia, retardation of growth, Deafnes", "lentigines, electrocardiographic conduction defects, 0cular hypertelorism, pulmonary stenosis, abnormalities of the genitals, retarded Growth, deafness", "Lentigines, Electrocardiographic Conduction Defects, Ocular Hypertelorism, Pulmonary Stenosis, Abnormalities of the Genitals, Retarded Growth, Deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Noonan syndrome with multiple lentigines", "shortest_name_length": 16}
{"curie": "MONDO:0060555", "names": ["VCRL2", "kynureninase deficiency, complete", "KYNURENINASE DEFICIENCY, COMPLETE", "CONGENITAL NAD DEFICIENCY DISORDER 2", "congenital NAD deficiency disorder 2", "vertebral, cardiac, renal, and limb defects syndrome 2", "VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vertebral, cardiac, renal, and limb defects syndrome 2", "shortest_name_length": 5}
{"curie": "MONDO:0043377", "names": ["JSpA", "Juvenile Spondyloarthritis", "juvenile Spondyloarthritis", "Juvenile spondyloarthritis", "Juvenile spondyloarthropathy", "juvenile spondyloarthropathy", "Juvenile Spondyloarthropathy", "juvenile spondyloarthropathies", "Juvenile spondyloarthropathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile spondyloarthropathy", "shortest_name_length": 4}
{"curie": "MONDO:0001553", "names": ["phacolytic glaucoma", "Phacolytic glaucoma", "glaucoma; phacolytic", "phacolytic; glaucoma", "Glaucoma, phacolytic", "Glaucoma, due to phacolysis", "Phacolytic glaucoma (disorder)", "phacolytic glaucoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phacolytic glaucoma", "shortest_name_length": 19}
{"curie": "UMLS:C3899658", "names": ["Gliosarcoma", "childhood gliosarcoma", "Childhood Gliosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Gliosarcoma", "shortest_name_length": 11}
{"curie": "MONDO:0800159", "names": ["disorder of polyamine metabolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of polyamine metabolism", "shortest_name_length": 32}
{"curie": "MONDO:0014263", "names": ["VRJS", "Del(8)(q24.3)", "Deletion 8q24.3", "Monosomy 8q24.3", "VERHEIJ SYNDROME", "Verheij syndrome", "8q24.3 microdeletion syndrome", "CHROMOSOME 8q24.3 DELETION SYNDROME", "chromosome 8Q24.3 deletion syndrome", "8q24.3 microdeletion syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "8q24.3 microdeletion syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C5555644", "names": ["Ovarian Smooth Muscle Tumor of Uncertain Malignant Potential", "Ovarian Smooth Muscle Neoplasm of Uncertain Malignant Potential"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Smooth Muscle Tumor of Uncertain Malignant Potential", "shortest_name_length": 60}
{"curie": "MONDO:0008114", "names": ["OCD", "Compulsion", "compulsion", "compulsions", "Compulsions", "COMPULSIVENESS", "compulsiveness", "Compulsion, NOS", "compulsive behavior", "Compulsive Behavior", "Compulsive behavior", "anancastic neurosis", "Anancastic neurosis", "Anankastic neurosis", "compulsive behaviour", "Compulsive behaviour", "Compulsive Behaviour", "compulsive behaviors", "Compulsive behaviors", "neurosis; anankastic", "Behavior, Compulsive", "anankastic; neurosis", "Compulsive Behaviors", "Behaviors, Compulsive", "Anankastic Personality", "Personality, Anankastic", "Anankastic Personalities", "Compulsive behavior, NOS", "Compulsive behaviour, NOS", "Personalities, Anankastic", "Obsessive compulsive neurosis", "obsessive compulsive disorder", "OBSESSIVE COMPULSIVE DISORDER", "Obsessive compulsive behavior", "obsessive-compulsive behavior", "OBSESSIVE-COMPULSIVE REACTION", "behavior obsessive compulsive", "Obsessive-compulsive disorder", "OBSESSIVE-COMPULSIVE NEUROSIS", "obsessive-compulsive disorder", "OBSESSIVE-COMPULSIVE DISORDER", "Disorder;obsessive-compulsive", "Obsessive-compulsive reaction", "Compulsive behavior (finding)", "Obsessive compulsive disorder", "obsessive-compulsive neurosis", "OBSESSIVE COMPULSIVE NEUROSIS", "Reaction obsessive-compulsive", "obsessive compulsive behavior", "Obsessive-compulsive behavior", "compulsive obsessive behavior", "REACTION OBSESSIVE-COMPULSIVE", "Obsessive Compulsive Neurosis", "Obsessive-compulsive neurosis", "BEHAVIOR OBSESSIVE COMPULSIVE", "obsessive compulsive neurosis", "Obsessive-Compulsive Neuroses", "Obsessive Compulsive Disorder", "compulsive behavior (symptom)", "Obsessive-Compulsive Disorder", "Obsessive-Compulsive Neurosis", "obsessive-compulsive disorders", "obsessive-compulsive; disorder", "obsessive-compulsive; neurosis", "Neuroses, Obsessive-Compulsive", "NEUROSIS, OBSESSIVE COMPULSIVE", "behaviour obsessive compulsive", "obsessive-compulsive; reaction", "disorder; obsessive-compulsive", "Obsessive-compulsive behaviour", "Obsessive compulsive behaviors", "Neurosis, obsessive compulsive", "Obsessive compulsive behaviour", "Obsessive-compulsive disorders", "Obsessive-Compulsive Disorders", "Neurosis, Obsessive-Compulsive", "reaction; obsessive-compulsive", "Disorder, Obsessive-Compulsive", "neurosis; obsessive-compulsive", "Neurosis, Obsessive Compulsive", "obsessive compulsive behaviour", "Disorders, Obsessive-Compulsive", "compulsions compulsive disorder", "Obsessive compulsive disorder, NOS", "OCD (obsessive compulsive disorder)", "OCD - Obsessive-compulsive disorder", "obsessive compulsive disorder (OCD)", "COMPULSIONS AND COMPULSIVE DISORDERS", "obsessive-compulsive behavior (symptom)", "Obsessive-compulsive disorder (disorder)", "obsessive compulsive disorder (diagnosis)", "obsessive-compulsive neurosis or reaction", "Obsessive-compulsive disorder, unspecified", "obsessive-compulsive psychoneurosis or reaction", "obsessive-compulsive disorder, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "obsessive-compulsive disorder", "shortest_name_length": 3}
{"curie": "MONDO:0015596", "names": ["encephalitis limbic non-herpetic acute", "Non-herpetic acute limbic encephalitis", "non-herpetic acute limbic encephalitis", "Non-herpetic acute limbic encephalitis (disorder)", "Non-herpetic acute limbic encephalitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-herpetic acute limbic encephalitis", "shortest_name_length": 38}
{"curie": "UMLS:C4055160", "names": ["Deep Morphea", "Deep Circumscribed Morphea"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Deep Circumscribed Morphea", "shortest_name_length": 12}
{"curie": "MONDO:0005430", "names": ["early onset hypertension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early onset hypertension", "shortest_name_length": 24}
{"curie": "UMLS:C0855099", "names": ["Stage II Small Lymphocytic Lymphoma", "stage II small lymphocytic lymphoma", "Small Lymphocytic Lymphoma Stage II", "small lymphocytic lymphoma, stage II", "Stage II B-Cell Small Lymphocytic Lymphoma", "B-Cell Small Lymphocytic Lymphoma Stage II", "B-cell small lymphocytic lymphoma stage II", "Ann Arbor Stage II Small Lymphocytic Lymphoma", "Small lymphocyte B lymphoma (Lukes-Collins Classification) stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-cell small lymphocytic lymphoma stage II", "shortest_name_length": 35}
{"curie": "MONDO:0014704", "names": ["KOGS", "Kosaki overgrowth syndrome", "KOSAKI OVERGROWTH SYNDROME", "Kosaki overgrowth syndrome (disorder)", "skeletal overgrowth-craniofacial dysmorphism-hyperelastic skin-white matter lesions syndrome", "Skeletal overgrowth-craniofacial dysmorphism-hyperelastic skin-white matter lesions syndrome", "Skeletal overgrowth, craniofacial dysmorphism, hyperelastic skin, white matter lesion syndrome", "SKELETAL OVERGROWTH WITH FACIAL DYSMORPHISM, HYPERELASTIC SKIN, WHITE MATTER LESIONS, AND NEUROLOGIC DETERIORATION", "skeletal overgrowth with Facial Dysmorphism, hyperelastic skin, White matter lesions, and neurologic deterioration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skeletal overgrowth-craniofacial dysmorphism-hyperelastic skin-white matter lesions syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C5204612", "names": ["Urethral Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urethral Melanoma", "shortest_name_length": 17}
{"curie": "UMLS:C3897347", "names": ["Transient Neonatal Hypoparathyroidism", "Transient neonatal hypoparathyroidism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transient neonatal hypoparathyroidism", "shortest_name_length": 37}
{"curie": "UMLS:C1960509", "names": ["Epidural lipomatosis", "epidural lipomatosis", "Epidural lipomatosis (disorder)", "epidural lipomatosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epidural lipomatosis", "shortest_name_length": 20}
{"curie": "UMLS:C4526730", "names": ["Lung Adenocarcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Adenocarcinoma by AJCC v7 Stage", "shortest_name_length": 36}
{"curie": "MONDO:0011032", "names": ["DFNA11", "autosomal dominant deafness 11", "Deafness, Autosomal Dominant 11", "DEAFNESS, AUTOSOMAL DOMINANT 11", "deafness, autosomal dominant 11", "deafness, autosomal dominant type 11", "autosomal dominant nonsyndromic deafness 11", "MYO7A autosomal dominant nonsyndromic deafness", "autosomal dominant nonsyndromic hearing loss 11", "autosomal dominant nonsyndromic deafness type 11", "autosomal dominant nonsyndromic deafness caused by mutation in MYO7A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 11", "shortest_name_length": 6}
{"curie": "MONDO:0017026", "names": ["ILD specific to adulthood", "interstitial lung disease specific to adulthood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "interstitial lung disease specific to adulthood", "shortest_name_length": 25}
{"curie": "MONDO:0043327", "names": ["CSF leak", "csf leakage", "CSF leakage", "CSF otorrhea", "CSF rhinorrhea", "spinal CSF leak", "Cerebrospinal fluid leak", "cerebrospinal fluid leak", "Cerebrospinal Fluid Leak", "fluid leak, cerebrospinal", "Fluid Leak, Cerebrospinal", "leak, cerebrospinal fluid", "Leak, Cerebrospinal Fluid", "cerebrospinal fluid Leaks", "Cerebrospinal Fluid Leaks", "leak; cerebrospinal fluid", "cerebrospinal fluid leaks", "Leaks, cerebrospinal fluid", "Fluid Leaks, Cerebrospinal", "fluid Leaks, cerebrospinal", "Leaks, Cerebrospinal Fluid", "cerebrospinal fluid leakage", "leakage cerebrospinal fluid", "Cerebrospinal Fluid Leakage", "Cerebrospinal fluid leakage", "cerebrospinal fluid; leakage", "cerebrospinal fluid Leakages", "Leakage, Cerebrospinal Fluid", "Cerebrospinal Fluid Leakages", "leakage, cerebrospinal fluid", "cerebrospinal fluid drainage", "Cerebrospinal Fluid Drainage", "fluid leakage, cerebrospinal", "Fluid Leakage, Cerebrospinal", "Leakage, cerebrospinal fluid", "drainage, cerebrospinal fluid", "fluid drainage, cerebrospinal", "Drainage, Cerebrospinal Fluid", "Leakages, Cerebrospinal Fluid", "Fluid Leakages, Cerebrospinal", "fluid Leakages, cerebrospinal", "Leakages, cerebrospinal fluid", "Fluid Drainage, Cerebrospinal", "Cerebrospinal Fluid Drainages", "cerebrospinal fluid Drainages", "csf - cerebrospinal fluid leak", "fluid Drainages, cerebrospinal", "Fluid Drainages, Cerebrospinal", "Leakage of cerebrospinal fluid", "CSF - Cerebrospinal fluid leak", "Drainages, Cerebrospinal Fluid", "Drainages, cerebrospinal fluid", "spinal cerebrospinal fluid leak", "Spinal Cerebrospinal Fluid Leak", "Cerebrospinal fluid leak (disorder)", "cerebrospinal fluid leak, traumatic", "Cerebrospinal fluid leak (diagnosis)", "Cerebrospinal fluid leak, unspecified", "cerebrospinal fluid leak, spontaneous", "cerebrospinal fluid leakage, traumatic", "cerebrospinal fluid drainage, traumatic", "cerebrospinal fluid leak, post-traumatic", "Subgaleal cerebrospinal fluid collection", "cerebrospinal fluid leakage, spontaneous", "cerebrospinal fluid; cerebrospinal, leak", "cerebrospinal fluid leak, post traumatic", "cerebrospinal fluid drainage, spontaneous", "spinal cerebrospinal fluid leak, traumatic", "spinal cerebrospinal fluid leak (diagnosis)", "cerebrospinal fluid leakage, post-traumatic", "cerebrospinal fluid leakage, post traumatic", "spinal cerebrospinal fluid leak, spontaneous", "cerebrospinal fluid drainage, post traumatic", "cerebrospinal fluid drainage, post-traumatic", "spinal cerebrospinal fluid leak, post traumatic", "spinal cerebrospinal fluid leak, post-traumatic", "Cerebrospinal fluid leakage (morphologic abnormality)", "disorders of central nervous system other specified CSF leak", "disorders of central nervous system other specified CSF leak spinal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebrospinal fluid leak", "shortest_name_length": 8}
{"curie": "MONDO:0019685", "names": ["FGFR3-related chondrodysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FGFR3-related chondrodysplasia", "shortest_name_length": 30}
{"curie": "MONDO:0016206", "names": ["idiopathic uveal effusion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic uveal effusion syndrome", "shortest_name_length": 34}
{"curie": "UMLS:C1336123", "names": ["Stage IA Retinoblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Retinoblastoma", "shortest_name_length": 23}
{"curie": "MONDO:0004253", "names": ["breast papillomatosis", "intraductal breast papillomatosis", "breast intraductal papillomatosis", "Breast Intraductal Papillomatosis", "intraductal papillomatosis of breast", "Breast Multiple Intraductal Papillomas", "intraductal papillomatosis of the breast", "Intraductal papillomatosis of the breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intraductal breast papillomatosis", "shortest_name_length": 21}
{"curie": "MONDO:0021839", "names": ["Spirochetosis", "spirochetosis", "Spirochaetosis", "spirochaetosis", "INFECT SPIROCHETE", "SPIROCHETE INFECT", "Spirochetosis, NOS", "Spirochetal disease", "spirochetes disease", "disease spirochetal", "Spirochete Infection", "Spirochaetal disease", "INFECT SPIROCHAETALES", "Spirochete Infections", "SPIROCHAETALES INFECT", "Spirochetal infection", "spirochetal infection", "Infection, Spirochete", "Infections, Spirochete", "infection; spirochetal", "spirochaetal infection", "spirochetal; infection", "Spirochaetal infection", "Spirochaetales Infection", "spirochaetales infection", "Spirochete infection NOS", "Infection, Spirochaetales", "Spirochaete infection NOS", "spirochaetales infections", "Spirochaetales Infections", "Spirochetal infection, NOS", "Infections, Spirochaetales", "Spirochetal infection (disorder)", "spirochetal infection (diagnosis)", "Spirochetal infection, unspecified", "Spirochaetal infection, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spirochaetales infections", "shortest_name_length": 13}
{"curie": "UMLS:C5446650", "names": ["Metastatic Endometrial Mixed Cell Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Endometrial Mixed Cell Adenocarcinoma", "shortest_name_length": 48}
{"curie": "UMLS:C0151629", "names": ["ERUPTION FIXED", "Fixed eruption", "FIXED ERUPTION", "Eruption fixed", "fixed eruption", "Fixed Eruption"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fixed eruption", "shortest_name_length": 14}
{"curie": "UMLS:C2981274", "names": ["Stage IVB Thyroid Gland Medullary Cancer", "Stage IVB Thyroid Gland Medullary Carcinoma", "Stage IVB Thyroid Gland Medullary Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Thyroid Gland Medullary Carcinoma AJCC v7", "shortest_name_length": 40}
{"curie": "MONDO:0007073", "names": ["Hanhart", "hanhart syndrome", "HANHART SYNDROME", "Hanhart syndrome", "Jussieu syndrome", "hanhart's syndrome", "Aglossia-Adactylia", "AGLOSSIA-ADACTYLIA", "Hanhart's syndrome", "aglossia-adactylia", "aglossia adactylia", "HYPOGLOSSIA-HYPODACTYLIA", "Hypoglossia-Hypodactylia", "hypoglossia-hypodactylia", "Aglossia-adactyly syndrome", "peromelia with micrognathia", "Micrognathia with peromelia", "Aglossia-adactylia syndrome", "aglossia-adactylia syndrome", "Peromelia with Micrognathism", "PEROMELIA WITH MICROGNATHISM", "peromelia with micrognathism", "OROMANDIBULAR LIMB HYPOPLASIA", "Oromandibular Limb Hypoplasia", "oromandibular limb hypoplasia", "Hanhart's syndrome (disorder)", "Hypoglossia-hypodactyly syndrome", "hypoglossia-hypodactyly syndrome", "hypoglossia-hypodactylia syndrome", "Aglossia-adactyly syndrome (disorder)", "Oromandibular limb hypogenesis complex"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypoglossia-hypodactyly syndrome", "shortest_name_length": 7}
{"curie": "MONDO:0006035", "names": ["Tubular adenocarcinoma", "stomach tubular adenocarcinoma", "Gastric Tubular Adenocarcinoma", "gastric tubular adenocarcinoma", "Tubular adenocarcinoma gastric", "tubular stomach adenocarcinoma", "Tubular Adenocarcinoma of Stomach", "tubular adenocarcinoma of stomach", "Tubular Adenocarcinoma of the Stomach", "tubular adenocarcinoma of the stomach", "tubular adenocarcinoma of stomach (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric tubular adenocarcinoma", "shortest_name_length": 22}
{"curie": "UMLS:C4708695", "names": ["Vasoocclusive pain episode in sickle cell disease", "Vaso-occlusive pain episode in sickle cell disease", "Vaso-occlusive pain co-occurrent and due to sickle cell disease", "Vaso-occlusive pain co-occurrent and due to sickle cell disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaso-occlusive pain episode in sickle cell disease", "shortest_name_length": 49}
{"curie": "UMLS:C5205935", "names": ["Prostate Wilms Tumor", "Prostate Nephroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Wilms Tumor", "shortest_name_length": 20}
{"curie": "UMLS:C5206662", "names": ["Penile Hemangioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Penile Hemangioma", "shortest_name_length": 17}
{"curie": "UMLS:C4682553", "names": ["Uterine Corpus Sarcoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Corpus Sarcoma by AJCC v8 Stage", "shortest_name_length": 39}
{"curie": "UMLS:C1333374", "names": ["Ectopic Parathormone Secretion", "Ectopic Parathormone Secretion Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ectopic Parathormone Secretion Syndrome", "shortest_name_length": 30}
{"curie": "MONDO:0035450", "names": ["aprosencephaly", "Aprosencephaly", "Aprosencephalies", "Aprosencephaly (disorder)", "aprosencephaly (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aprosencephaly", "shortest_name_length": 14}
{"curie": "MONDO:0012538", "names": ["NEM7", "Nemaline Myopathy 7", "NEMALINE MYOPATHY 7", "nemaline myopathy 7", "CFL2 nemaline myopathy", "nemaline myopathy type 7", "nemaline myopathy 7, autosomal recessive", "nemaline myopathy caused by mutation in CFL2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nemaline myopathy 7", "shortest_name_length": 4}
{"curie": "MONDO:0010628", "names": ["immunoglobulin M, level of", "IMMUNOGLOBULIN M, LEVEL OF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunoglobulin M, level of", "shortest_name_length": 26}
{"curie": "MONDO:0001186", "names": ["DEPERSONALIZATION", "depersonalisation", "Depersonalization", "Depersonalisation", "depersonalization", "Depersonalizations", "neurotic derealization", "Neurotic derealization", "feel that body is unreal", "Feels own self is unreal", "depersonalisation syndrome", "depersonalization syndrome", "Depersonalization neurosis", "depersonalization disorder", "Depersonalization syndrome", "depersonalization neurosis", "Depersonalization disorder", "Depersonalisation neurosis", "Depersonalisation disorder", "Depersonalization Disorder", "Depersonalisation syndrome", "Depersonalization Disorders", "disorder; depersonalization", "Depersonalization (finding)", "depersonalization; disorder", "syndrome; depersonalization", "Disorder, Depersonalization", "Neurosis, depersonalization", "depersonalization; syndrome", "Disorders, Depersonalization", "feel that body is unreal (symptom)", "Depersonalization disorder (disorder)", "depersonalization disorder (diagnosis)", "feel that the body is unreal (depersonalization)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "depersonalization disorder", "shortest_name_length": 17}
{"curie": "UMLS:C5446563", "names": ["Lacrimal Sac Mucosa-Associated Lymphoid Tissue Lymphoma", "Lacrimal Drainage System Mucosa-Associated Lymphoid Tissue Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lacrimal Drainage System Mucosa-Associated Lymphoid Tissue Lymphoma", "shortest_name_length": 55}
{"curie": "UMLS:C4553847", "names": ["Stage IV Urethral Cancer", "Stage IV Urethral Cancer AJCC v8", "Stage IV Urethral Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Urethral Cancer AJCC v8", "shortest_name_length": 24}
{"curie": "MONDO:0010564", "names": ["DCB", "CBD", "deuteranopia", "Deuteranopia", "Deutan Defect", "Deutan defect", "deutan defect", "Deuteranomaly", "Defect, Deutan", "GREEN COLORBLINDNESS", "Green colorblindness", "DEUTAN COLORBLINDNESS", "Deutan colorblindness", "colorblindness, deutan", "Reduced red-green vision", "Deutan defect (red-green)", "Red-Green Color Blindness", "deutan defect (diagnosis)", "Red-green dyschromatopsia", "blindness color green red", "red-green color blindness", "Red green color blindness", "red green color blindness", "Red-green color blindness", "Color Blindness, Red Green", "red-green colour blindness", "Red-green colour blindness", "Red green colour blindness", "Color Blindness, Red-Green", "Red/green color vision defect", "Red-green color vision defect", "Red/green colour vision defect", "Reduced red-green discrimination", "reduced red-green discrimination", "partial achromatopsia, deutan type", "colorblindness, partial, DEUTAN series", "Dyschromatopsia with red-green confusion", "Reduced red-green discrimination (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "red-green color blindness", "shortest_name_length": 3}
{"curie": "MONDO:0000763", "names": ["epithelial and subepithelial dystrophy", "epithelial and subepithelial corneal dystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epithelial and subepithelial corneal dystrophy", "shortest_name_length": 38}
{"curie": "MONDO:0018443", "names": ["FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome", "shortest_name_length": 84}
{"curie": "MONDO:0005013", "names": ["DDCHS", "Dedifferentiated chondrosarcoma", "Dedifferentiated Chondrosarcoma", "dedifferentiated chondrosarcoma", "Dedifferentiated chondrosarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dedifferentiated chondrosarcoma", "shortest_name_length": 5}
{"curie": "UMLS:C4724729", "names": ["Metastatic Oral Cavity Mucoepidermoid Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Oral Cavity Mucoepidermoid Carcinoma", "shortest_name_length": 47}
{"curie": "UMLS:C5557253", "names": ["Chemotherapy Related Agranulocytosis", "Chemotherapy-Related Agranulocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chemotherapy Related Agranulocytosis", "shortest_name_length": 36}
{"curie": "MONDO:0003417", "names": ["Lhermitte's syndrome", "lhermitte's syndrome", "Internuclear Ophthalmoplegia", "INTERNUCLEAR OPHTHALMOPLEGIA", "internuclear ophthalmoplegia", "Internuclear ophthalmoplegia", "Internuclear Ophthalmoplegias", "Ophthalmoplegia, Internuclear", "internuclear; ophthalmoplegia", "ophthalmoplegia; internuclear", "Ophthalmoplegia internuclearis", "Ophthalmoplegias, Internuclear", "Bielschowsky-Lutz-Cogan syndrome", "INO - Internuclear ophthalmoplegia", "Internuclear ophthalmoplegia (disorder)", "internuclear ophthalmoplegia (diagnosis)", "other specified disorders of binocular movement internuclear ophthalmoplegia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "internuclear ophthalmoplegia", "shortest_name_length": 20}
{"curie": "UMLS:C0334547", "names": ["Aggressive Osteoblastoma", "Aggressive osteoblastoma", "Aggressive osteoblastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aggressive osteoblastoma", "shortest_name_length": 24}
{"curie": "MONDO:0005807", "names": ["CD4+ T-Lymphocytopenia", "CD4+ T Lymphocytopenia", "T-Lymphocytopenia, CD4+", "CD4+ T-Lymphocytopenias", "T-Lymphocytopenias, CD4+", "Idiopathic CD4+ T Lymphocytopenia", "Idiopathic CD4+ T-Lymphocytopenia", "T-Lymphocytopenia, Idiopathic CD4+", "CD4+ T Lymphocytopenia, Idiopathic", "T Lymphocytopenia, Idiopathic CD4+", "CD4+ T-Lymphocytopenia, Idiopathic", "Idiopathic CD4-Positive T-Lymphocytopenia", "idiopathic CD4-positive T-lymphocytopenia", "Idiopathic CD4 Positive T-Lymphocytopenia", "T Lymphocytopenia, Idiopathic CD4 Positive", "CD4 Positive T Lymphocytopenia, Idiopathic", "T-Lymphocytopenia, Idiopathic CD4-Positive", "CD4-Positive T-Lymphocytopenia, Idiopathic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic CD4-positive T-lymphocytopenia", "shortest_name_length": 22}
{"curie": "MONDO:0005749", "names": ["eosinophilic pneumonia", "Pneumonia eosinophilic", "EOSINOPHILIC PNEUMONIA", "PNEUMONIA EOSINOPHILIC", "Eosinophilic pneumonia", "Eosinophilic Pneumonia", "pneumonia eosinophilic", "Pneumonia, Eosinophilic", "eosinophilic; pneumonia", "Eosinophilic Pneumonias", "pneumonia, eosinophilic", "Pneumonia, eosinophilic", "pneumonia; eosinophilic", "Pneumonias, Eosinophilic", "EP - Eosinophilic pneumonia", "Eosinophilic pneumonia, NOS", "Eosinophilic pneumonia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eosinophilic pneumonia", "shortest_name_length": 22}
{"curie": "UMLS:C0341714", "names": ["Renal Lymphoma", "Kidney Lymphoma", "kidney lymphoma", "lymphoma of kidney", "Lymphoma of kidney", "Primary Renal Lymphoma", "Primary Kidney Lymphoma", "Lymphoma of kidney (disorder)", "lymphoma of kidney (diagnosis)", "Lymphomatous infiltrate of kidney"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoma of kidney", "shortest_name_length": 14}
{"curie": "UMLS:C1328332", "names": ["Procedural hypertension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Procedural hypertension", "shortest_name_length": 23}
{"curie": "UMLS:C1881258", "names": ["Ionizing Radiation Toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ionizing Radiation Toxicity", "shortest_name_length": 27}
{"curie": "MONDO:0037254", "names": ["Transitional Cell Tumor", "transitional cell tumor", "Transitional cell neoplasm", "transitional cell neoplasm", "Transitional Cell Neoplasm", "Transitional cell papilloma and carcinoma", "Transitional Cell Papillomas and Carcinomas", "TRANSITIONAL CELL PAPILLOMAS AND CARCINOMAS", "Transitional cell papilloma AND/OR carcinoma", "Transitional cell neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transitional cell neoplasm", "shortest_name_length": 23}
{"curie": "UMLS:C1335036", "names": ["Non-Neoplastic Renal Disorder", "Non-Neoplastic Kidney Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Kidney Disorder", "shortest_name_length": 29}
{"curie": "UMLS:C5400991", "names": ["OCI", "Overt Stroke", "Overt Cerebral Infarction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Overt Stroke", "shortest_name_length": 3}
{"curie": "MONDO:0013787", "names": ["PMRED", "NEDHCS", "PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM", "psychomotor retardation, epilepsy, and craniofacial dysmorphism", "neurodevelopmental disorder with hypotonia, craniofacial abnormalities, and seizures", "NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, CRANIOFACIAL ABNORMALITIES, AND SEIZURES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "psychomotor retardation, epilepsy, and craniofacial dysmorphism", "shortest_name_length": 5}
{"curie": "UMLS:C0543698", "names": ["hypersensitive syndrome", "syndrome hypersensitive", "Hypersensitive syndrome", "Hypersensitivity disease", "Hypersensitivity Diseases", "hypersensitivity syndrome", "Hypersensitivity syndrome", "hypersensitivity diseases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypersensitive syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0014390", "names": ["Hypt13", "hypt13", "HYPT13", "HYPOTRICHOSIS 13", "hypotrichosis 13", "KRT71 hypotrichosis", "hypotrichosis type 13", "HYPOTRICHOSIS WITH WOOLLY HAIR", "hypotrichosis with woolly hair", "hypotrichosis caused by mutation in KRT71"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotrichosis 13", "shortest_name_length": 6}
{"curie": "MONDO:0007726", "names": ["BHD", "BFHD", "BEUKES HIP DYSPLASIA", "Beukes hip dysplasia", "hip dysplasia Beukes type", "Hip dysplasia Beukes type", "Beukes type hip dysplasia", "Hip dysplasia, Beukes type", "Hip Dysplasia, Beukes Type", "Cilliers-Beighton syndrome", "hip dysplasia, Beukes type", "Cilliers Beighton syndrome", "HIP DYSPLASIA, BEUKES TYPE", "Beukes familial hip dysplasia", "BEUKES FAMILIAL HIP DYSPLASIA", "Beukes Familial Hip Dysplasia", "Hip dysplasia Beukes type (disorder)", "Premature degenerative osteoarthropathy of hip", "Osteoarthropathy, Premature Degenerative, of Hip", "osteoarthropathy, premature degenerative, of hip", "OSTEOARTHROPATHY, PREMATURE DEGENERATIVE, OF HIP", "premature degenerative osteoarthropathy of the hip", "Premature degenerative osteoarthropathy of the hip"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hip dysplasia, Beukes type", "shortest_name_length": 3}
{"curie": "MONDO:0009606", "names": ["METHEMOGLOBINEMIA, TYPE I", "methemoglobinemia, type I", "methemoglobinemia, type 2", "Methemoglobinemia, Type I", "methemoglobinemia, type 1", "Methemoglobinemia, Type Ii", "METHEMOGLOBINEMIA, TYPE II", "methemoglobinemia, type II", "NADH diaphorase deficiency", "NADH cytochrome B5 reductase deficiency", "NADH methemoglobin reductase deficiency", "NADH-cytochrome B5 reductase deficiency", "NADH-CYTOCHROME b5 REDUCTASE DEFICIENCY, TYPE I", "NADH-cytochrome B5 reductase deficiency, type 1", "Nadh-Cytochrome B5 Reductase Deficiency, Type I", "NADH-cytochrome B5 reductase deficiency, type 2", "NADH-CYTOCHROME b5 REDUCTASE DEFICIENCY, TYPE II", "Nadh-Cytochrome B5 Reductase Deficiency, Type Ii", "NADH-dependent methemoglobin reductase deficiency", "methemoglobinemia, congenital, autosomal recessive", "methemoglobinemia due to deficiency of methemoglobin reductase"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "methemoglobinemia due to deficiency of methemoglobin reductase", "shortest_name_length": 25}
{"curie": "UMLS:C0271561", "names": ["GHD", "ghd", "STH deficiency", "Somatotropin Deficiency", "Somatotropin deficiency", "somatotropin deficiency", "hormone growth deficiency", "Growth hormone deficiency", "growth hormone deficiency", "deficiency growth hormone", "deficiency; growth hormone", "growth hormone; deficiency", "Growth hormone insufficiency", "Somatotropin deficiency, NOS", "growth hormone insufficiency", "growth hormones insufficiency", "Growth hormone deficiency, NOS", "GHD - Growth hormone deficiency", "Growth hormone deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Somatotropin deficiency", "shortest_name_length": 3}
{"curie": "UMLS:C4285755", "names": ["Bladder Neuroendocrine Carcinoma", "Neuroendocrine carcinoma of the bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neuroendocrine carcinoma of the bladder", "shortest_name_length": 32}
{"curie": "MONDO:0022894", "names": ["craniosynostosis autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniosynostosis autosomal dominant", "shortest_name_length": 35}
{"curie": "UMLS:C0751530", "names": ["Aneurysmal Subarachnoid Hemorrhage", "Subarachnoid Hemorrhage, Aneurysmal", "Aneurysmal Subarachnoid Hemorrhages", "Hemorrhage, Aneurysmal Subarachnoid", "Hemorrhages, Aneurysmal Subarachnoid", "Subarachnoid Hemorrhages, Aneurysmal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subarachnoid Hemorrhage, Aneurysmal", "shortest_name_length": 34}
{"curie": "MONDO:0017445", "names": ["Acheiria", "acheiria", "Absent hand", "agenesis; hand", "hand; agenesis", "Forepaw apodia", "Agenesis of hand", "Amelia of the hand", "Agenesis of forepaw", "congenital absence of hand", "Congenital absence of hand", "Agenesis of hand (disorder)", "congenital hand deformity absence", "Congenital absence of hand (disorder)", "congenital absence of hand (diagnosis)", "Transverse deficiency of arm, wrist level"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acheiria", "shortest_name_length": 8}
{"curie": "MONDO:0100344", "names": ["BARTS1", "Bartter disease type 1", "Type 1 Bartter Syndrome", "Bartter syndrome type 1", "Bartter syndrome type I", "Bartter Syndrome, Type 1", "SLC12A1 Bartter syndrome", "Bartter syndrome, type 1", "Bartter's syndrome type 1", "antenatal Bartter syndrome", "hyperprostaglandin E syndrome", "HYPERPROSTAGLANDIN E SYNDROME 1", "hyperprostaglandin E syndrome 1", "Hyperprostaglandin E syndrome 1", "Hyperprostaglandin E Syndrome 1", "Bartter syndrome, furosemide type", "antenatal Bartter syndrome type 1", "Bartter syndrome antenatal type 1", "Bartter syndrome type 1 antenatal", "Antenatal Bartter syndrome type 1", "Bartter syndrome, antenatal type 1", "Bartter syndrome, type 1, antenatal", "Bartter syndrome, antenatal, type 1", "BARTTER SYNDROME, TYPE 1, ANTENATAL", "Bartter Syndrome, Antenatal, Type 1", "Hyperprostaglandin E syndrome type 1", "Bartter syndrome, furosemide-amiloride type", "Bartter syndrome antenatal type 1 (disorder)", "Bartter syndrome antenatal type 1 (diagnosis)", "Bartter syndrome caused by mutation in SLC12A1", "Hypokalemic alkalosis with hypercalciuria, antenatal", "hypokalemic alkalosis with hypercalciuria 1 antenatal", "hypokalemic alkalosis with hypercalciuria antenatal 1", "Hypokalemic Alkalosis with Hypercalciuria 1, Antenatal", "HYPOKALEMIC ALKALOSIS WITH HYPERCALCIURIA 1, ANTENATAL", "hypokalemic alkalosis with hypercalciuria 1, antenatal", "hypokalemic alkalosis with hypercalciuria, antenatal, 1", "Hypokalemic Alkalosis With Hypercalciuria, Antenatal, 1", "Hypokalemic alkalosis with hypercalciuria antenatal type 1", "Hypokalaemic alkalosis with hypercalciuria antenatal type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bartter disease type 1", "shortest_name_length": 6}
{"curie": "UMLS:C0745499", "names": ["Junctional bradycardia", "Junctional Bradycardia", "JUNCTIONAL BRADYCARDIA", "Junctional Bradycardia by EKG Finding", "Junctional Bradycardia by ECG Finding"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Junctional bradycardia", "shortest_name_length": 22}
{"curie": "UMLS:C4683570", "names": ["Lugano Classification Stage IIE Adult Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage IIE Adult Lymphoma AJCC v8", "shortest_name_length": 54}
{"curie": "MONDO:0054850", "names": ["ODG6", "OVARIAN DYSGENESIS 6", "ovarian dysgenesis 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian dysgenesis 6", "shortest_name_length": 4}
{"curie": "UMLS:C1334003", "names": ["Barrett's esophagus high grade dysplasia", "Barrett's oesophagus high grade dysplasia", "High Grade Dysplasia in Barrett Esophagus", "High Grade Dysplasia in Barrett's Esophagus", "Barretts esophagus with high grade dysplasia", "Barrett's esophagus with high grade dysplasia", "Barretts oesophagus with high grade dysplasia", "Barretts esophagus with high grade dysplasia (disorder)", "Barrett's esophagus with high grade dysplasia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Barretts esophagus with high grade dysplasia", "shortest_name_length": 40}
{"curie": "MONDO:0006673", "names": ["Basophil Adenoma", "Basophil adenoma", "basophil adenoma", "Adenoma, Basophil", "Basophil Adenomas", "basophilic adenoma", "Basophilic Adenoma", "Adenomas, Basophil", "mucoid cell adenoma", "Mucoid cell adenoma", "Adenoma, Basophilic", "Basophilic Adenomas", "Mucoid Cell Adenoma", "Adenomas, Basophilic", "Pituitary Basophilic Adenoma", "pituitary basophilic adenoma", "basophilic adenoma, pituitary", "adenoma, basophilic, pituitary", "pituitary gland basophil adenoma", "Pituitary Gland Basophil Adenoma", "pituitary gland basophilic adenoma", "Pituitary gland Basophilic adenoma", "Basophilic Pituitary Gland Adenoma", "basophilic pituitary gland adenoma", "Basophil adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pituitary gland basophil adenoma", "shortest_name_length": 16}
{"curie": "UMLS:C5419606", "names": ["Advanced Follicular Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Follicular Lymphoma", "shortest_name_length": 28}
{"curie": "UMLS:C3267049", "names": ["Chronic graft versus host disease in intestine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic graft versus host disease in intestine", "shortest_name_length": 46}
{"curie": "MONDO:0001551", "names": ["vulva ulcer", "Ulcer;vulva", "ulcer vulva", "ulcer; vulva", "Vulvar ulcer", "vulval ulcer", "vulvar ulcer", "ulcers vulva", "vulva; ulcer", "Vulva ulceration", "vulvar ulceration", "Vulvar ulceration", "Vulval ulceration", "VULVAR ULCERATION", "Ulcer NOS of vulva", "Ulceration of vulva", "ulceration of vulva", "Ulceration of vulva, NOS", "Ulceration of vulva (disorder)", "ulceration of vulva (diagnosis)", "ulceration of vulva unspecified", "vulvar ulcer (physical finding)", "Ulceration of vulva, unspecified", "vulvar ulceration in diseases classified elsewhere", "Ulceration of vulva in disease classified elsewhere", "Ulceration of vulva associated with another disorder", "Ulceration of vulva in diseases classified elsewhere", "vulvar ulceration in diseases classified elsewhere (diagnosis)", "Ulceration of vulva associated with another disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ulceration of vulva", "shortest_name_length": 11}
{"curie": "MONDO:0008422", "names": ["SIDBA4", "ANEMIA, SIDEROBLASTIC, 4", "anemia, sideroblastic, 4", "autosomal dominant sideroblastic anemia", "Autosomal dominant sideroblastic anemia", "Autosomal dominant sideroblastic anaemia", "sideroblastic anemia, autosomal dominant", "autosomal dominant sideroblastic anemia 4", "anemia, sideroblastic, autosomal dominant", "Anemia, Sideroblastic, Autosomal Dominant", "Autosomal dominant sideroblastic anemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant sideroblastic anemia", "shortest_name_length": 6}
{"curie": "MESH:D008106", "names": ["Liver Cirrhosis, Experimental"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liver Cirrhosis, Experimental", "shortest_name_length": 29}
{"curie": "UMLS:C1334243", "names": ["Intracranial Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intracranial Melanoma", "shortest_name_length": 21}
{"curie": "MONDO:0033201", "names": ["DFNB57", "autosomal recessive deafness 57", "deafness, autosomal recessive 57", "DEAFNESS, AUTOSOMAL RECESSIVE 57", "hearing loss, autosomal recessive 57", "autosomal recessive nonsyndromic deafness 57"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal recessive 57", "shortest_name_length": 6}
{"curie": "MONDO:0005981", "names": ["paralysis tick", "tick paralysis", "Tick paralysis", "TICK PARALYSIS", "Tick Paralyses", "Tick Paralysis", "tick; paralysis", "Paralyses, Tick", "Paralysis, Tick", "paralysis; tick", "Tick bite paralysis", "Tick paralysis (disorder)", "tick paralysis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tick paralysis", "shortest_name_length": 14}
{"curie": "MONDO:0100463", "names": ["methylmalonic aciduria and/or homocystinuria, cblD type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "methylmalonic aciduria and/or homocystinuria, cblD type", "shortest_name_length": 55}
{"curie": "MONDO:0020401", "names": ["congenital unguarded mitral orifice"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital unguarded mitral orifice", "shortest_name_length": 35}
{"curie": "UMLS:C4744758", "names": ["Thyroid Gland Lymphangioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Lymphangioma", "shortest_name_length": 26}
{"curie": "UMLS:C3272424", "names": ["Gastric Glomus Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Glomus Tumor", "shortest_name_length": 20}
{"curie": "UMLS:C0392008", "names": ["Anesthetic complication", "anesthetic complication", "anesthesia complication", "anesthesia complications", "Anaesthetic complication", "anaesthesia complication", "complications anesthesia", "anesthetic complications", "anesthesia; complication", "anaesthetic complications", "anesthetics complications", "anaesthesia complications", "complications; anesthesia", "anaesthetics complications", "Complication of anesthesia", "complication of anesthesia", "Complication of anaesthesia", "COMPLICATIONS OF ANESTHESIA", "Anesthetic complication NOS", "complications of anesthesia", "Anaesthetic complication NOS", "Complication of anesthesia, NOS", "Complication of anaesthesia, NOS", "Complication of anesthesia (disorder)", "complications of anesthesia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Complication of anesthesia", "shortest_name_length": 23}
{"curie": "MONDO:0013712", "names": ["SMDP5", "CSF2RB DEFICIENCY", "Csf2Rb deficiency", "PAP DUE TO CSF2RB DEFICIENCY", "Pap due to Csf2Rb deficiency", "PULMONARY ALVEOLAR PROTEINOSIS 5", "pulmonary alveolar proteinosis 5", "surfactant metabolism dysfunction, pulmonary, 5", "SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 5", "CSF2RB hereditary pulmonary alveolar proteinosis", "surfactant metabolism dysfunction, pulmonary, type 5", "hereditary pulmonary alveolar proteinosis caused by mutation in CSF2RB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "surfactant metabolism dysfunction, pulmonary, 5", "shortest_name_length": 5}
{"curie": "MONDO:0016059", "names": ["Lowry-Yong syndrome", "Lowry Yong syndrome", "Cleft lip/palate-deafness-sacral lipoma syndrome", "cleft lip/palate-deafness-sacral lipoma syndrome", "Cleft lip/palate-hearing loss-sacral lipoma syndrome", "Cleft palate and cleft lip with deafness and sacral lipoma syndrome", "Cleft palate and cleft lip with deafness and sacral lipoma syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleft lip/palate-deafness-sacral lipoma syndrome", "shortest_name_length": 19}
{"curie": "MONDO:0030712", "names": ["OPDM4", "OCULOPHARYNGODISTAL MYOPATHY 4", "oculopharyngodistal myopathy 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculopharyngodistal myopathy 4", "shortest_name_length": 5}
{"curie": "MONDO:0012346", "names": ["GEFS+4", "GEFSP4", "GEFSP, Type 4", "Gefs+, type 4", "GEFS+, TYPE 4", "generalised epilepsy with febrile seizures plus 4", "generalized epilepsy with febrile seizures plus 4", "generalised epilepsy with febrile seizures plus type 4", "generalized epilepsy with febrile seizures plus type 4", "GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 4", "generalized epilepsy with febrile seizures plus, type 4", "Generalized Epilepsy With Febrile Seizures Plus, Type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "generalized epilepsy with febrile seizures plus, type 4", "shortest_name_length": 6}
{"curie": "MONDO:0018123", "names": ["autosomal recessive intellectual disability due to TRAPPC9 deficiency", "intellectual disability-obesity-brain malformations-facial dysmorphism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability-obesity-brain malformations-facial dysmorphism syndrome", "shortest_name_length": 69}
{"curie": "MONDO:0027696", "names": ["voriconazole toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "voriconazole toxicity", "shortest_name_length": 21}
{"curie": "UMLS:C0518454", "names": ["Open Head Injury", "open head injury", "Injury, Open Head", "Head Injury, Open", "Open Head Injuries", "open head injuries", "Open head injuries", "Head Injuries, Open", "Injuries, Open Head"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Head Injury, Open", "shortest_name_length": 16}
{"curie": "MONDO:0019171", "names": ["LQTS", "Romano-Ward syndrome", "Ward-Romano syndrome", "familial long QT syndrome", "Familial long QT syndrome", "Inherited long QT syndrome", "congenital long qt syndrome", "Congenital long QT syndrome", "long qt syndrome congenital", "congenital long QT syndrome", "Long QT syndrome congenital", "hereditary long QT syndrome", "Romano-Ward long QT syndrome", "Congenital long QT syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial long QT syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C5419060", "names": ["Oligometastatic Prostate Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oligometastatic Prostate Carcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0013025", "names": ["del(6q25)", "Del(6)(q25)", "Monosomy 6q25", "deletion 6q25", "monosomy 6q25", "6q25 microdeletion syndrome", "CHROMOSOME 6q24-q25 DELETION SYNDROME", "chromosome 6q24-q25 deletion syndrome", "chromosome 6q25-q25 deletion syndrome", "chromosome 6q25 microdeletion syndrome", "6q25 microdeletion syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 6q24-q25 deletion syndrome", "shortest_name_length": 9}
{"curie": "MONDO:0100454", "names": ["GUCY2D retinopathy", "retinopathy caused by mutation in GUCY2D"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "GUCY2D retinopathy", "shortest_name_length": 18}
{"curie": "MONDO:0021004", "names": ["BRACHYDACTYLY", "Brachydactyly", "brachydactyly", "Brachydactylia", "Brachydactylias", "Brachydactylism", "Brachydactylies", "Brachydactylisms", "Short fingers or toes", "Brachydactyly syndrome", "brachydactyly (disease)", "brachydactyly was noted", "Brachydactyly (disorder)", "brachydactyly (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly", "shortest_name_length": 13}
{"curie": "UMLS:C5236018", "names": ["Post-Surgical Complication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post-Surgical Complication", "shortest_name_length": 26}
{"curie": "UMLS:C1336883", "names": ["Urethral Condyloma", "Urethral Condylomata", "Condylomata of Urethra", "Condylomata of the Urethra", "Urethral Condyloma Acuminatum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urethral Condyloma Acuminatum", "shortest_name_length": 18}
{"curie": "UMLS:C4683637", "names": ["Childhood Hodgkin Lymphoma by Ann Arbor Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Hodgkin Lymphoma by Ann Arbor Stage", "shortest_name_length": 45}
{"curie": "UMLS:C0000735", "names": ["ABDOMEN TUMOR", "tumor abdomen", "abdomen tumors", "abdomen tumours", "Abdominal tumor", "abdominal tumor", "Abdomen--Tumors", "tumor abdominal", "abdomen neoplasm", "Abdominal tumour", "tumor of abdomen", "Tumor of abdomen", "abdominal tumors", "abdominal tumours", "abdominals tumors", "Tumour of abdomen", "Abdominal Neoplasm", "Abdominal neoplasm", "abdominal neoplasm", "Neoplasm, Abdominal", "Neoplasm of abdomen", "Abdominal Neoplasms", "Neoplasms, Abdominal", "Abdominal neoplasm NOS", "Neoplasm of abdomen (disorder)", "Neoplasm of abdomen (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abdominal Neoplasms", "shortest_name_length": 13}
{"curie": "MONDO:0015975", "names": ["HIGM with susceptibility to opportunistic infections", "hyper-IgM syndrome with susceptibility to opportunistic infections"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyper-IgM syndrome with susceptibility to opportunistic infections", "shortest_name_length": 52}
{"curie": "UMLS:C0280165", "names": ["Stage III Lymphoblastic Lymphoma", "Stage III Adult Lymphoblastic Lymphoma", "Adult Lymphoblastic Lymphoma Stage III", "Adult Stage III Lymphoblastic Lymphoma", "stage III adult lymphoblastic lymphoma", "adult lymphoblastic lymphoma, stage III", "Ann Arbor Stage III Adult Lymphoblastic Lymphoma", "Stage III Adult Precursor Lymphoblastic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Adult Lymphoblastic Lymphoma", "shortest_name_length": 32}
{"curie": "MONDO:0005844", "names": ["Chalazia", "chalazia", "Chalazion", "CHALAZION", "chalazion", "chalazions", "tarsal cyst", "Tarsal cyst", "Cyst;meibomian", "Meibomian Cyst", "meibomian cyst", "Meibomian cyst", "cyst, Meibomian", "meibomian; cyst", "meibomians cyst", "cysts meibomian", "Cyst, Meibomian", "cyst; meibomian", "Meibomian gland cyst", "chalazion (diagnosis)", "Meibomian (gland) cyst", "Cyst of meibomian gland", "chalazion (physical finding)", "meibomian gland lipogranuloma", "Meibomian gland lipogranuloma", "Cyst of meibomian gland (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chalazion", "shortest_name_length": 8}
{"curie": "UMLS:C1335366", "names": ["Parotid Gland Sebaceous Lymphadenoma", "Sebaceous Lymphadenoma of the Parotid Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parotid Gland Sebaceous Lymphadenoma", "shortest_name_length": 36}
{"curie": "MONDO:0010697", "names": ["OPEM", "MYOPIA-OPHTHALMOPLEGIA SYNDROME", "Myopia-Ophthalmoplegia Syndrome", "myopia-ophthalmoplegia syndrome", "ophthalmoplegia, external, and myopia", "OPHTHALMOPLEGIA, EXTERNAL, AND MYOPIA", "Ophthalmoplegia, External, and Myopia", "OPHTHALMOPLEGIA, EXTERNAL, AND MYOPIA (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ophthalmoplegia, external, and myopia", "shortest_name_length": 4}
{"curie": "NCIT:C112006", "names": ["Masaoka Staging", "Masaoka Staging System", "Thymoma by Masaoka-Koga Stage", "Masaoka Staging System for Thymoma", "Masaoka-Koga Staging System for Thymoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thymoma by Masaoka-Koga Stage", "shortest_name_length": 15}
{"curie": "MONDO:0006197", "names": ["Endometrial Small Cell Carcinoma", "endometrial small cell carcinoma", "endometrium small cell carcinoma", "small cell carcinoma of endometrium", "Endometrial Small Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometrial small cell carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0100039", "names": ["CDKL5", "CDKL5 disorder", "CDKL5-related disorder", "CDKL5 inherited genetic disease", "inherited genetic disease caused by mutation in CDKL5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CDKL5 disorder", "shortest_name_length": 5}
{"curie": "MONDO:0015433", "names": ["R17", "Ring 17", "Ring chromosome 17", "Chromosome 17 ring", "ring chromosome 17", "chromosome 17 ring", "Ring chromosome type 17", "Ring chromosome 17 syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ring chromosome 17", "shortest_name_length": 3}
{"curie": "MONDO:0018960", "names": ["CGM", "congenital megalo-ureter", "congenital giant megaureter", "congenital primary megaureter", "Congenital primary megaureter", "congenital primary megalo-ureter", "Congenital primary megalo-ureter", "Congenital primary megaureter (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital primary megaureter", "shortest_name_length": 3}
{"curie": "MONDO:0019246", "names": ["disorder of lysosomal amino acid transport", "inborn disorder of lysosomal amino acid transport"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of lysosomal amino acid transport", "shortest_name_length": 42}
{"curie": "UMLS:C0948224", "names": ["Stenotrophomonas infection", "Stenotrophomonas maltophilia infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stenotrophomonas infection", "shortest_name_length": 26}
{"curie": "MONDO:0019264", "names": ["NAGA deficiency type 3", "Schindler disease type 3", "alpha-N-acetylgalactosaminidase deficiency type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alpha-N-acetylgalactosaminidase deficiency type 3", "shortest_name_length": 22}
{"curie": "MONDO:0060761", "names": ["NEDEHCC", "NEURODEVELOPMENTAL DISORDER WITH EPILEPSY AND HYPOPLASIA OF THE CORPUS CALLOSUM", "neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum", "shortest_name_length": 7}
{"curie": "MONDO:0800087", "names": ["type 11 collagen-related bone disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type 11 collagen-related bone disorder", "shortest_name_length": 38}
{"curie": "UMLS:C0262518", "names": ["Stage IIIA Hodgkin Lymphoma", "Hodgkin's Disease Stage IIIA", "HODGKIN'S DISEASE STAGE IIIA", "Stage IIIA Hodgkin's Disease", "Hodgkin's Lymphoma Stage IIIA", "Stage IIIA Hodgkin's Lymphoma", "Ann Arbor Stage IIIA Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage IIIA Hodgkin Lymphoma", "shortest_name_length": 27}
{"curie": "MONDO:0016487", "names": ["beta-thalassemia intermedia", "Beta thalassemia intermedia", "Beta-thalassemia intermedia", "THALASSEMIA BETA INTERMEDIA", "BETA-THALASSEMIA INTERMEDIA", "Beta thalassaemia intermedia", "Beta thalassemia intermedia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "beta-thalassemia intermedia", "shortest_name_length": 27}
{"curie": "MONDO:0018576", "names": ["non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy", "shortest_name_length": 97}
{"curie": "MONDO:0012731", "names": ["EL1", "4.1- trait", "4.1- TRAIT", "4.1-Minus Trait", "4.1-minus trait", "4.1-MINUS TRAIT", "elliptocytosis-1", "elliptocytosis 1", "Elliptocytosis 1", "ELLIPTOCYTOSIS 1", "elliptocytosis type 1", "EPB41 hereditary elliptocytosis", "elliptocytosis, Rhesus-linked type", "ELLIPTOCYTOSIS, RHESUS-LINKED TYPE", "Elliptocytosis, Rhesus-Linked Type", "Protein 4.1 of erythrocyte Membrane, defect of", "Protein 4.1 of Erythrocyte Membrane, Defect of", "PROTEIN 4.1 OF ERYTHROCYTE MEMBRANE, DEFECT OF", "hereditary elliptocytosis caused by mutation in EPB41"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "elliptocytosis 1", "shortest_name_length": 3}
{"curie": "MONDO:0003477", "names": ["brainstem ependymoma", "brain stem ependymoma", "Brain Stem Ependymoma", "ependymoma of brainstem", "Ependymoma of brain stem", "ependymoma of brain stem", "ependymoma of the brainstem", "Ependymoma of the Brainstem", "ependymoma of the brain stem", "Ependymoma of brain stem (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brain stem ependymoma", "shortest_name_length": 20}
{"curie": "MONDO:0100387", "names": ["AML, Monosomy 7", "acute myeloid leukemia, Monosomy 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, Monosomy 7", "shortest_name_length": 15}
{"curie": "MONDO:0019536", "names": ["D+HUS", "Sxt-HUS", "typical HUS", "Shiga-like toxin-associated HUS", "typical hemolytic-uremic syndrome", "hemolytic-uremic syndrome with diarrhea", "D-plus hemolytic uremic syndrome (D+HUS)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "typical hemolytic-uremic syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0010405", "names": ["HPCX2", "PROSTATE CANCER, HEREDITARY, X-LINKED 2", "Prostate Cancer, Hereditary, X-Linked 2", "prostate cancer, hereditary, X-linked 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate cancer, hereditary, X-linked 2", "shortest_name_length": 5}
{"curie": "UMLS:C1608953", "names": ["Intestinal diaphragm disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal diaphragm disease", "shortest_name_length": 28}
{"curie": "MONDO:0005894", "names": ["PCM", "Lutz", "Almeida", "Splendore", "lobo disease", "Paracoccidioidomycose", "paracoccidiodomycosis", "PARACOCCIDIOIDOMYCOSIS", "Paracoccidioidomycosis", "Paracoccidioidomycoses", "paracoccidioidomycosis", "Brazilian blastomycosis", "Brazilian; blastomycotic", "paracoccidioidal mycosis", "Paracoccidioides infection", "Paracoccidioidal granuloma", "Paracoccidioides Infection", "Paracoccidioidal Granuloma", "Infection, Paracoccidioides", "Granuloma, Paracoccidioidal", "Paracoccidioides Infections", "GRANULOMA, PARACOCCIDIOIDAL", "Paracoccidioides infections", "Paracoccidioidal Granulomas", "South American Blastomycosis", "south American blastomycosis", "South American blastomycosis", "South American; blastomycotic", "blastomycosis; South American", "BLASTOMYCOSIS, SOUTH AMERICAN", "Blastomycosis, South American", "Paracoccidioides infection NOS", "LUTZ-SPLENDORE-ALMEIDA DISEASE", "Lutz-Splendore-Almeida disease", "Paracoccidioidomycosis (disorder)", "paracoccidioidomycosis (diagnosis)", "Paracoccidioidomycosis, unspecified", "Infection by Blastomyces brasiliensis", "Paracoccidioides brasiliensis; infection", "Mucocutaneous South American blastomycosis", "Infection by Paracoccidioides brasiliensis", "infection; Blastomyces, blastomycotic, Brazilian", "mucocutaneous-lymphangitic paracoccidioidomycosis", "paracoccidioidomycosis mucocutaneous-lymphangitis", "Mucocutaneous-lymphangitic paracoccidioidomycosis", "mucocutaneous-lymphangitic; paracoccidioidomycosis", "paracoccidioidomycosis; mucocutaneous-lymphangitic", "infection; Blastomyces, blastomycotic, South American", "Mucocutaneous-lymphangitic paracoccidioidomycosis (disorder)", "Mucocutaneous-lymphangitic paracoccidioidomycosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paracoccidioidomycosis", "shortest_name_length": 3}
{"curie": "MONDO:0003970", "names": ["Gastric Fundus Cancer", "gastric fundus cancer", "Cancer of Gastric Fundus", "gastric fundus carcinoma", "cancer of gastric fundus", "Gastric Fundus Carcinoma", "cancer of Fundus of stomach", "carcinoma of gastric fundus", "fundus of stomach carcinoma", "cancer of fundus of stomach", "Carcinoma of Gastric Fundus", "Cancer of Fundus of Stomach", "cancer of the gastric fundus", "Cancer of the Gastric Fundus", "carcinoma of fundus of stomach", "Carcinoma of fundus of stomach", "Carcinoma of Fundus of Stomach", "gastric fundus (stomach) cancer", "carcinoma of the gastric fundus", "Carcinoma of the Gastric Fundus", "Gastric Fundus (Stomach) Cancer", "gastric malignant carcinoma fundus", "cancer of the fundus of the stomach", "Cancer of the Fundus of the Stomach", "Carcinoma of the Fundus of the Stomach", "carcinoma of the fundus of the stomach", "Carcinoma of fundus of stomach (disorder)", "Carcinoma of fundus of stomach (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric fundus carcinoma", "shortest_name_length": 21}
{"curie": "UMLS:C4683591", "names": ["Lugano Classification Advanced Stage Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Advanced Stage Hodgkin Lymphoma AJCC v8", "shortest_name_length": 61}
{"curie": "MONDO:0017356", "names": ["ornithine; metabolic disorder", "Ornithine metabolism disorder", "metabolic disorder; ornithine", "disorder of ornithine metabolism", "Disorder of ornithine metabolism", "Disorders of ornithine metabolism", "ornithine metabolism disturbances", "inborn disorder of ornithine metabolism", "inborn error of ornithine metabolic process", "inborn ornithine metabolic process disorder", "Disorder of ornithine metabolism (disorder)", "ornithine metabolism disturbances (diagnosis)", "rare inborn error of ornithine metabolic process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of ornithine metabolism", "shortest_name_length": 29}
{"curie": "MONDO:0012920", "names": ["T1D21", "IDDM21", "TYPE 1 DIABETES MELLITUS 21", "type 1 diabetes mellitus 21", "insulin-dependent diabetes mellitus 21", "Insulin-Dependent Diabetes Mellitus 21", "DIABETES MELLITUS, INSULIN-DEPENDENT, 21", "Diabetes Mellitus, Insulin-Dependent, 21", "diabetes mellitus, insulin-dependent, 21", "DIABETES MELLITUS, INSULIN-DEPENDENT, 21 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type 1 diabetes mellitus 21", "shortest_name_length": 5}
{"curie": "MONDO:0002459", "names": ["DTH", "Delayed Hypersensitivity", "Type IV Hypersensitivity", "type iv hypersensitivity", "hypersensitivity type iv", "hypersensitivity iv type", "type IV hypersensitivity", "Delayed hypersensitivity", "delayed hypersensitivity", "Hypersensitivity, Type IV", "Hypersensitivity, Delayed", "Type IV Hypersensitivities", "Delayed Hypersensitivities", "immunoproliferative disease", "cell-mediated immune reaction", "Cell-mediated immune reaction", "delayed-type hypersensitivity", "Delayed-Type Hypersensitivity", "delayed type hypersensitivity", "Delayed type hypersensitivity", "Cell mediated immune reaction", "cell mediated hypersensitivity", "tuberculin type hypersensitivity", "Type 4 Hypersensitivity Reaction", "type IV hypersensitivity disease", "Type 4 hypersensitivity reaction", "type 4 hypersensitivity reaction", "Tuberculin-Type Hypersensitivity", "Tuberculin Type Hypersensitivity", "Gell and Coombs reaction type IV", "Type IV hypersensitivity reaction", "Hypersensitivity reaction type IV", "CELL-MEDIATED IMMUNOLOGICAL REACT", "type IV hypersensitivity reaction", "Delayed hypersensitivity reaction", "Type IV Hypersensitivity Reaction", "Cell-mediated immunological react", "delayed hypersensitivity reaction", "Hypersensitivity, Tuberculin-Type", "Hypersensitivity, Tuberculin Type", "Delayed Hypersensitivity Reaction", "delayed hypersensitivity response", "delayed hypersensitivity reactions", "Tuberculin-Type Hypersensitivities", "CELL MEDIATED IMMUNOLOGICAL REACTION", "Cell mediated immunological reaction", "disorder of type IV hypersensitivity", "Cell-mediated immunological reaction", "delayed-type hypersensitivity response", "Delayed-Type Hypersensitivity Response", "Cell-mediated immune reaction (disorder)", "hypersensitivity reaction type IV disease", "cell-mediated immune reaction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type IV hypersensitivity disease", "shortest_name_length": 3}
{"curie": "UMLS:C0276353", "names": ["influenza B", "influenza type B", "influenza B (diagnosis)", "Influenza due to Influenza B virus", "Influenza caused by Influenza B virus", "Influenza due to Influenza virus, type B", "Influenza caused by Influenza B virus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Influenza due to Influenza virus, type B", "shortest_name_length": 11}
{"curie": "UMLS:C5239374", "names": ["Metastatic Mucosal Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Mucosal Melanoma", "shortest_name_length": 27}
{"curie": "UMLS:C0521506", "names": ["Injection site paresthesia", "Injection site paraesthesia", "Injection site paresthesia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site paresthesia", "shortest_name_length": 26}
{"curie": "MONDO:0005541", "names": ["spondylolyses", "Spondylolyses", "spondylolysis", "Spondylolysis", "spondylolysis (disease)", "Spondylolysis (disorder)", "spondylolysis (diagnosis)", "Pars interarticularis defect", "Spondylolysis, site unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondylolysis", "shortest_name_length": 13}
{"curie": "MONDO:0012110", "names": ["IGF1 DEFICIENCY", "IGF1 Deficiency", "IGF1 deficiency", "IGF-I Deficiency", "IGF-1 deficiency", "Insulin Growth Factor I Deficiency", "Insulin-like Growth Factor I Deficiency", "INSULIN-LIKE GROWTH FACTOR I DEFICIENCY", "insulin-like growth factor I deficiency", "insulin-like growth Factor 1 deficiency", "Insulin-Like Growth Factor I Deficiency", "Primary insulin-like growth factor deficiency", "primary insulin-like growth factor deficiency", "IGF-1 (insulin-like growth factor 1) deficiency", "Growth delay-deafness-intellectual disability syndrome", "growth delay-deafness- intellectual disability syndrome", "Growth delay, deafness, intellectual disability syndrome", "Growth delay-hearing loss-intellectual disability syndrome", "Growth delay due to insulin-like growth factor type 1 deficiency", "growth delay due to insulin-like growth factor type 1 deficiency", "growth retardation with sensorineural deafness and mental retardation", "Growth Retardation with Sensorineural Deafness and Mental Retardation", "GROWTH RETARDATION WITH SENSORINEURAL DEAFNESS AND MENTAL RETARDATION", "growth retardation with sensorineural deafness and intellectual disability", "Growth delay due to insulin-like growth factor type 1 deficiency (disorder)", "growth retardation with deafness and mental retardation due to IGF1 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "growth delay due to insulin-like growth factor type 1 deficiency", "shortest_name_length": 15}
{"curie": "MONDO:0014736", "names": ["CMT2Z", "MORC2 Charcot-Marie-Tooth disease", "Charcot-Marie-Tooth neuropathy type 2Z", "Charcot-Marie-Tooth neuropathy, type 2Z", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2Z", "Charcot-Marie-Tooth disease axonal type 2Z", "Charcot-Marie-Tooth disease, axonal, type 2Z", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Z", "Charcot-Marie-Tooth disease, axonal, type 2z", "autosomal dominant Charcot-Marie-Tooth disease type 2Z", "Autosomal dominant Charcot-Marie-Tooth disease type 2Z", "Charcot-Marie-Tooth disease caused by mutation in MORC2", "autosomal dominant axonal Charcot-Marie-Tooth disease type 2Z", "Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2Z", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2Z", "Autosomal dominant Charcot-Marie-Tooth disease type 2Z (disorder)", "autosomal dominant Charcot-Marie-Tooth disease type 2Z (diagnosis)", "Autosomal dominant Charcot-Marie-Tooth disease type 2 due to MORC2 mutation", "autosomal dominant Charcot-Marie-Tooth disease type 2 due to MORC2 mutation", "Autosomal dominant Charcot-Marie-Tooth disease type 2 due to MORC2 (MORC family CW-type zinc finger 2) mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease axonal type 2Z", "shortest_name_length": 5}
{"curie": "MONDO:0005122", "names": ["Pectobacterium infectious disease", "Pectobacterium disease or disorder", "Pectobacterium carotovorum infection", "Pectobacterium caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pectobacterium carotovorum infection", "shortest_name_length": 33}
{"curie": "MONDO:0003983", "names": ["synchronous bilateral breast carcinoma", "Synchronous Bilateral Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "synchronous bilateral breast carcinoma", "shortest_name_length": 38}
{"curie": "MONDO:0033261", "names": ["DFNA34", "autosomal dominant nonsyndromic deafness 34", "DEAFNESS, AUTOSOMAL DOMINANT 34, WITH OR WITHOUT INFLAMMATION", "deafness, autosomal dominant 34, with or without inflammation", "hearing loss, autosomal dominant 34, with or without inflammation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal dominant 34, with or without inflammation", "shortest_name_length": 6}
{"curie": "MONDO:0018393", "names": ["male infertility with azoospermia or oligozoospermia due to single gene mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "male infertility with azoospermia or oligozoospermia due to single gene mutation", "shortest_name_length": 80}
{"curie": "UMLS:C0264286", "names": ["Ulcerative pharyngitis", "Pharyngitis ulcerative", "ulcerative pharyngitis", "Pharyngitis, ulcerative", "Ulcerative pharyngitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ulcerative pharyngitis", "shortest_name_length": 22}
{"curie": "UMLS:C3272830", "names": ["Colorectal MALT Lymphoma", "Colorectal Mucosa-Associated Lymphoid Tissue Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Mucosa-Associated Lymphoid Tissue Lymphoma", "shortest_name_length": 24}
{"curie": "MONDO:0017124", "names": ["Noma", "noma", "NOMA", "Nomas", "nomas", "Cancrum oris", "cancrum oris", "Cancrum Oris", "oral gangrene", "oro-facial noma", "noma neonatorum", "oro-facial gangrene", "Gangrenous Stomatitis", "Gangrenous stomatitis", "gangrenous stomatitis", "gangrenous; stomatitis", "Stomatitis, Gangrenous", "stomatitis; gangrenous", "Gangrenous Stomatitides", "Cancrum oris (disorder)", "cancrum oris (diagnosis)", "Stomatitides, Gangrenous", "Acute gangrenous stomatitis", "gangrenous stomatitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "noma", "shortest_name_length": 4}
{"curie": "MONDO:0010354", "names": ["AHDS", "T3 RESISTANCE", "T3 Resistance", "T3 resistance", "T3 resisitence", "MCT8 deficiency", "ALLAN-Herndon syndrome", "Allan-Herndon syndrome", "ALLAN-HERNDON SYNDROME", "TRIIODOTHYRONINE RESISTANCE", "Triiodothyronine Resistance", "triiodothyronine resistence", "triiodothyronine resistance", "ALLAN-HERNDON-DUDLEY SYNDROME", "ALLAN-Herndon-DUDLEY syndrome", "Allan-Herndon-Dudley syndrome", "Allan-Herndon-Dudley Syndrome", "Allan-Herndon-Dudley syndrome (AHDS)", "mental retardation and muscular atrophy", "Mental retardation and muscular atrophy", "MENTAL RETARDATION AND MUSCULAR ATROPHY", "Monocarboxylate transporter-8 deficiency", "monocarboxylate transporter 8 deficiency", "monocarboxylate transporter-8 deficiency", "Monocarboxylate Transporter 8 Deficiency", "Monocarboxylate transporter 8 deficiency", "MONOCARBOXYLATE TRANSPORTER 8 DEFICIENCY", "X-linked mental retardation with hypotonia", "MENTAL RETARDATION, X-LINKED, WITH HYPOTONIA", "mental retardation, X-linked, with hypotonia", "Mental Retardation, X-Linked, With Hypotonia", "intellectual disability and muscular atrophy", "Monocarboxylate Transporter 8 (Mct8) Deficiency", "X-linked intellectual disability with hypotonia", "intellectual disability, X-linked, with hypotonia", "X-linked intellectual disability-hypotonia syndrome", "Monocarboxylate transporter 8 deficiency (disorder)", "MCT8-Specific Thyroid Hormone Cell Membrane Transporter Deficiency", "MCT8-specific thyroid hormone cell Membrane transporter deficiency", "Mct8 (Slc16a2)-Specific Thyroid Hormone Cell Transporter Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Allan-Herndon-Dudley syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C5670653", "names": ["ELP1-Medulloblastoma Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ELP1-Medulloblastoma Syndrome", "shortest_name_length": 29}
{"curie": "MONDO:0022804", "names": ["colobomata unilobar lung heart defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colobomata unilobar lung heart defect", "shortest_name_length": 37}
{"curie": "MONDO:0006640", "names": ["Hypercorticism", "hypercorticism", "Hyperadrenalism", "HYPERADRENALISM", "hyperadrenalism", "Hypercortisolism", "HYPERCORTISONISM", "HYPERCORTISOLISM", "Cushing syndrome", "Hypercortisonism", "hypercortisolism", "Hypercortisolemia", "hypercortisolemia", "Hypercorticoidism", "Hypercortisolaemia", "Hyperadrenocorticism", "hyperadrenocorticism", "HYPERADRENOCORTICISM", "Hypercorticism adrenal", "Overproduction of ACTH", "Hyperadrenocorticalism", "ADRENAL HYPERCORTICISM", "HYPERCORTICISM ADRENAL", "Adrenal hypercorticism", "Suprarenogenic syndrome", "Hyperadrenalcorticalism", "cortisol overproduction", "Adrenal Cushing syndrome", "overproduction of cortisol", "Overproduction of cortisol", "Adrenal Cushing's syndrome", "adrenal gland hyperfunction", "Hypercortisolism (disorder)", "adrenocortical overactivity", "Adrenal Gland Hyperfunction", "adrenocortical hyperfunction", "Adrenocortical Hyperfunction", "ADRENAL CORTEX HYPERFUNCTION", "hyperfunction, adrenal gland", "Adrenocortical hyperfunction", "adrenal cortex hyperfunction", "Adrenal hyperadrenocorticism", "Hyperfunction, Adrenal Gland", "Adrenal cortex hyperfunction", "Increased cortisol production", "hyperfunction, adrenocortical", "Hyperadrenocorticism, adrenal", "Hyperfunction, Adrenocortical", "adrenal cortical hyperfunction", "Adrenal cortical hyperfunctions", "Increased circulating cortisol level", "Adrenocortical hyperactivity syndrome", "Adrenal Cushing's syndrome (disorder)", "adrenocortical overactivity (diagnosis)", "Adrenal dependent hyperadrenalcorticism", "disorder of corticoadrenal overactivity", "Adrenocortical hyperfunction (disorder)", "Disorder of corticoadrenal overactivity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adrenal gland hyperfunction", "shortest_name_length": 14}
{"curie": "UMLS:C0730274", "names": ["Vitreomacular traction syndrome", "Vitreomacular traction syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vitreomacular traction syndrome", "shortest_name_length": 31}
{"curie": "UMLS:C4687705", "names": ["Pericardial Yolk Sac Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pericardial Yolk Sac Tumor", "shortest_name_length": 26}
{"curie": "MONDO:0020428", "names": ["Gerbode defect", "Congenital Gerbode defect", "congenital Gerbode defect", "left ventricular-to-right atrial communication", "Left ventricular-to-right atrial communication", "ventricular septal defect between left ventricle and right atrium", "Ventricular septal defect between left ventricle and right atrium", "Ventricular septal defect between left ventricle and right atrium (disorder)", "ventricular septal defect between left ventricle and right atrium (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital Gerbode defect", "shortest_name_length": 14}
{"curie": "MONDO:0017049", "names": ["Boylan-dew syndrome", "hypomyelination neuropathy-arthrogryposis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypomyelination neuropathy-arthrogryposis syndrome", "shortest_name_length": 19}
{"curie": "UMLS:C4683498", "names": ["Recurrent Extensive Stage Lung Small Cell Carcinoma", "Recurrent Extensive Stage Small Cell Lung Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Extensive Stage Lung Small Cell Carcinoma", "shortest_name_length": 51}
{"curie": "MONDO:0008899", "names": ["Camptodactyly syndrome Guadalajara type 2", "Guadalajara camptodactyly syndrome type 2", "camptodactyly syndrome Guadalajara type 2", "Guadalajara camptodactyly syndrome type II", "camptodactyly syndrome, Guadalajara type 2", "Camptodactyly syndrome, Guadalajara type 2", "camptodactyly syndrome, Guadalajara, type 2", "Camptodactyly Syndrome, Guadalajara, Type II", "CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE II", "camptodactyly syndrome, Guadalajara, type II", "Camptodactyly syndrome Guadalajara type 2 (disorder)", "[OBSOLETE] Camptodactyly Syndrome, Guadalajara, Type II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "camptodactyly syndrome, Guadalajara type 2", "shortest_name_length": 41}
{"curie": "UMLS:C5555101", "names": ["Penile Mucosal Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Penile Mucosal Melanoma", "shortest_name_length": 23}
{"curie": "MONDO:0005078", "names": ["CSP", "phyllode tumor", "phyllodes tumor", "Phyllodes tumor", "tumor phyllodes", "Phyllodes Tumor", "Phyllodes tumour", "Tumor, Phyllodes", "phyllodes; tumor", "phyllodes tumors", "phyllodes tumour", "Phyllodes Tumors", "tumor; phyllodes", "phyllode tumours", "phyllodes tumours", "Tumors, Phyllodes", "phyllodes neoplasm", "Phyllodes Neoplasm", "Phyllodes tumor NOS", "Phyllodes tumor, NOS", "Phyllodes tumour NOS", "Phyllodes tumour, NOS", "Cystosarcoma Phyllodes", "Cystosarcoma phyllodes", "cystosarcoma phyllodes", "Cystosarcoma phylloides", "cystosarcoma phylloides", "Cystosarcoma Phylloides", "Cystosarcoma phyllodes, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phyllodes tumor", "shortest_name_length": 3}
{"curie": "UMLS:C2981705", "names": ["stage IV eyelid carcinoma", "Stage IV Eyelid Carcinoma", "Stage IV Eyelid Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Eyelid Carcinoma AJCC v7", "shortest_name_length": 25}
{"curie": "MONDO:0008399", "names": ["SS1", "sarcoidosis", "SARCOIDOSIS", "Boeck sarcoid", "BOECK SARCOID", "HLA-DRB1 sarcoidosis", "susceptibility to sarcoidosis 1", "sarcoidosis, susceptibility to, 1", "SARCOIDOSIS, SUSCEPTIBILITY TO, 1", "sarcoidosis, susceptibility to, type 1", "sarcoidosis caused by mutation in HLA-DRB1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sarcoidosis, susceptibility to, 1", "shortest_name_length": 3}
{"curie": "UMLS:C3898280", "names": ["Mixed Morphea"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mixed Morphea", "shortest_name_length": 13}
{"curie": "MONDO:0021809", "names": ["dysautonomia", "Dysautonomias", "primary dysautonomia", "Primary Dysautonomias", "dysautonomia, primary", "Dysautonomias, primary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary dysautonomia", "shortest_name_length": 12}
{"curie": "UMLS:C4764225", "names": ["Recurrent Desmoplastic Small Round Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Desmoplastic Small Round Cell Tumor", "shortest_name_length": 45}
{"curie": "UMLS:C0264265", "names": ["nasal necrosis", "Nasal necrosis", "necrosis; nose", "Necrosis nasal", "nose; necrosis", "NECROSIS NASAL", "Necrosis of nose", "nasal necrosis (diagnosis)", "Necrosis of nose (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Necrosis of nose", "shortest_name_length": 14}
{"curie": "UMLS:C1519659", "names": ["Tubal Diverticulosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tubal Diverticulosis", "shortest_name_length": 20}
{"curie": "MONDO:0019100", "names": ["NMO", "SMON", "NMOSD", "Devic", "Devic Disease", "devic disease", "DEVIC DISEASE", "Devic disease", "Disease, Devic", "Devic syndrome", "devic syndrome", "devics disease", "Devics Disease", "Devic Syndrome", "devic's disease", "Devic's disease", "Syndrome, Devic", "Devics Syndrome", "Devic's Disease", "devics syndrome", "devic's syndrome", "Devic's Syndrome", "Disease, Devic's", "Devic's syndrome", "Syndrome, Devic's", "Optic neuromyelitis", "optic neuromyelitis", "NEUROMYELITIS OPTICA", "neuromyelitis optica", "Neuromyelitis optica", "optic; neuromyelitis", "Neuromyelitis Optica", "Neuro-optic myelitis", "neuromyelitis; optic", "NMO Spectrum Disorder", "ophthalmoneuromyelitis", "NMO Spectrum Disorders", "OPHTHALMONEUROMYELITIS", "Devic disease (diagnosis)", "devic neuromyelitis optica", "Devic Neuromyelitis Optica", "Devic Neuromyelitis Opticas", "MYELITIS, OPTIC NEURITIS IN", "Devics Neuromyelitis Optica", "Neuromyelitis Optica, Devic", "Neuromyelitis optica [Devic]", "Neuromyelitis Opticas, Devic", "Devic's Neuromyelitis Optica", "Devic's neuromyelitis optica", "Neuromyelitis Optica, Devic's", "neuritis optica; demyelination", "SUBACUTE MYELOOPTICONEUROPATHY", "NEUROENCEPHALOMYELOPATHY, OPTIC", "Subacute myelo-opticoneuropathy", "neuroencephalomyelopathy; optic", "Subacute myelo-optic neuropathy", "Neuromyelitis optica (disorder)", "Neuromyelitis Optica Spectrum Disorder", "Neuromyelitis optica spectrum disorder", "SMON - subacute myelo-optico-neuropathy", "Neuromyelitis Optica Spectrum Disorders", "Neuromyelitis Optica (NMO) Spectrum Disorder", "Neuromyelitis Optica (NMO) Spectrum Disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuromyelitis optica", "shortest_name_length": 3}
{"curie": "UMLS:C0853897", "names": ["Diabetic cardiomyopathy", "Diabetic Cardiomyopathy", "cardiomyopathy diabetic", "diabetic cardiomyopathy", "Cardiomyopathy, Diabetic", "Diabetic Cardiomyopathies", "Cardiomyopathies, Diabetic", "diabetic cardiomyopathy (diagnosis)", "Cardiomyopathy due to diabetes mellitus", "Cardiomyopathy due to diabetes mellitus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diabetic Cardiomyopathies", "shortest_name_length": 23}
{"curie": "MONDO:0005777", "names": ["donovanosis", "DONOVANOSIS", "Donovanosis", "Donovanosis;M", "Donovanosis;F", "pudendal ulcer", "Pudendal ulcer", "Granuloma pudendi", "GRANULOMA PUDENDI", "Granuloma Donovani", "Granuloma venereum", "pudendi; granuloma", "granuloma; pudendi", "Granuloma Venereum", "GRANULOMA VENEREUM", "GRANULOMA INGUINALE", "inguinal; granuloma", "granuloma inguinale", "Granuloma Inguinale", "Granuloma inguinale", "granuloma; venereum", "venereum; granuloma", "granuloma; inguinale", "GI - Granuloma inguinale", "Ulcerating granuloma pudendi", "Granuloma inguinale (disorder)", "granuloma inguinale (diagnosis)", "GRANULOMA INGUINALE DONOVANOSIS", "GRANULOMA INGUINALE <DONOVANOSIS>", "Infection due to Donovania granulomatis", "Calymmatobacterium granulomatis infection", "Calymmatobacterium granulomatis; infection", "infection; Calymmatobacterium granulomatis", "Infection due to Calymmatobacterium granulomatis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "granuloma inguinale", "shortest_name_length": 11}
{"curie": "UMLS:C0278718", "names": ["CLL Stage 0", "Stage 0 CLL", "CLL, stage 0", "stage 0 chronic lymphocytic leukemia", "Chronic Lymphocytic Leukemia Stage 0", "Chronic lymphocytic leukemia stage 0", "Stage 0 Chronic Lymphocytic Leukemia", "Chronic lymphocytic leukaemia stage 0", "lymphocytic leukemia, stage 0 chronic", "leukemia, stage 0 chronic lymphocytic", "chronic lymphocytic Leukemia, stage 0", "Stage 0 Chronic Lymphocytic Leukemia (CLL)", "Stage 0 Chronic Lymphocytic Leukemia- Modified Rai Staging System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic lymphocytic leukemia stage 0", "shortest_name_length": 11}
{"curie": "UMLS:C4744439", "names": ["Unresectable Lung Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Lung Carcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C0406284", "names": ["SDRIFE", "Baboon syndrome", "syndrome baboon", "baboon syndrome", "Symmetrical drug-related intertriginous and flexural exanthema", "Symmetrical drug-related intertriginous and flexural exanthema (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Baboon syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0011418", "names": ["DYX3", "DYSLEXIA, SUSCEPTIBILITY TO, 3", "dyslexia, susceptibility to, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyslexia, susceptibility to, 3", "shortest_name_length": 4}
{"curie": "MONDO:0012965", "names": ["BFIC4", "BFIS4", "benign familial infantile seizures 4", "Benign Familial Infantile Seizures, 4", "Seizures, Benign Familial Infantile, 4", "SEIZURES, BENIGN FAMILIAL INFANTILE, 4", "seizures, benign familial infantile, 4", "Convulsions, Benign Familial Infantile, 4", "convulsions, benign familial infantile, 4", "CONVULSIONS, BENIGN FAMILIAL INFANTILE, 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "seizures, benign familial infantile, 4", "shortest_name_length": 5}
{"curie": "MONDO:0017165", "names": ["bile acid CoA ligase deficiency and defective amidation", "Bile acid CoA ligase deficiency and defective amidation", "Bile acid coenzyme A ligase deficiency and defective amidation", "Bile acid coenzyme A ligase deficiency and defective amidation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bile acid CoA ligase deficiency and defective amidation", "shortest_name_length": 55}
{"curie": "MONDO:0002742", "names": ["cervical mucinous adenocarcinoma", "Cervical Mucinous Adenocarcinoma", "mucinous adenocarcinoma of cervix", "uterine cervix mucinous adenocarcinoma", "mucinous adenocarcinoma of cervix (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical mucinous adenocarcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0021783", "names": ["STREP THROAT", "Strep Throat", "strep throat", "Strep throat", "Strept throat", "strept throat", "strep throats", "Septic pharyngitis", "Septic sore throat", "SEPTIC SORE THROAT", "septic sore throat", "pharyngitis; septic", "septic; pharyngitis", "septic; sore throat", "sore throat; septic", "streptococcal angina", "Streptococcal angina", "EPIDEMIC SORE THROAT", "PHARYNGITIS STREPTOCOCCUS", "Sore throat;streptococcal", "Streptococcal sore throat", "Pharyngitis streptococcal", "Streptococcal Pharyngitis", "streptococcal sore throat", "STREPTOCOCCAL PHARYNGITIS", "streptococcal pharyngitis", "streptococcus pharyngitis", "Streptococcal pharyngitis", "Pharyngitis;streptococcal", "streptoccocal; sore throat", "PHARYNGITIS, STREPTOCOCCAL", "pharyngitis; streptoccocal", "streptoccocal; pharyngitis", "sore throat; streptoccocal", "Streptococcal sore throat (disorder)", "streptococcal sore throat (diagnosis)", "Septic sore throat due to streptococcal infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "streptococcal sore throat", "shortest_name_length": 12}
{"curie": "MONDO:0008349", "names": ["CIUFFO SYNDROME", "Ciuffo syndrome", "Ciuffo Syndrome", "PULMONIC STENOSIS, ATRIAL SEPTAL DEFECT, AND UNIQUE ELECTROCARDIOGRAPHIC ABNORMALITIES", "Pulmonic Stenosis, Atrial Septal Defect, and Unique Electrocardiographic Abnormalities", "pulmonic stenosis, atrial septal defect, and unique electrocardiographic abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonic stenosis, atrial septal defect, and unique electrocardiographic abnormalities", "shortest_name_length": 15}
{"curie": "UMLS:C4744458", "names": ["Locally Advanced Pancreatic Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Pancreatic Neuroendocrine Carcinoma", "shortest_name_length": 52}
{"curie": "UMLS:C0159783", "names": ["open fracture of metacarpal bone", "Open Fracture of Metacarpal Bone", "Open fracture of metacarpal bone", "Open fracture of metacarpal bones", "Fracture of metacarpal bones, open", "Open fracture of metacarpal bone(s)", "Open fracture of metacarpal bone, NOS", "Open fracture of metacarpal bone (disorder)", "open fracture of metacarpal bone (diagnosis)", "Open fracture of metacarpal bone, site unspecified", "Open fracture of metacarpal bones, site unspecified", "Open fracture of metacarpal bone(s), site unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Open fracture of metacarpal bone", "shortest_name_length": 32}
{"curie": "UMLS:C1332569", "names": ["Blastoid Variant Mantle Cell Lymphoma", "Classic Blastoid Variant Mantle Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Blastoid Variant Mantle Cell Lymphoma", "shortest_name_length": 37}
{"curie": "MONDO:0060564", "names": ["HELIX", "HELIX syndrome", "HELIX SYNDROME", "hypohidrosis, electrolyte imbalance, lacrimal gland dysfunction, ichthyosis, and xerostomia", "HYPOHIDROSIS, ELECTROLYTE IMBALANCE, LACRIMAL GLAND DYSFUNCTION, ICHTHYOSIS, AND XEROSTOMIA", "Hypohidrosis-electrolyte imbalance-lacrimal gland dysfunction-ichthyosis-xerostomia syndrome", "hypohidrosis-electrolyte imbalance-lacrimal gland dysfunction-ichthyosis-xerostomia syndrome", "Hypohidrosis, electrolyte imbalance, lacrimal gland dysfunction, ichthyosis, xerostomia syndrome", "HELIX (hypohidrosis, electrolyte imbalance, lacrimal gland dysfunction, ichthyosis, xerostomia) syndrome", "Hypohidrosis, electrolyte imbalance, lacrimal gland dysfunction, ichthyosis, xerostomia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HELIX syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0015093", "names": ["sub-cortical nodular heterotopia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sub-cortical nodular heterotopia", "shortest_name_length": 32}
{"curie": "UMLS:C0542147", "names": ["Jejunal Perforation", "Perforation jejunal", "jejunal perforation", "Jejunal perforation", "jejunum perforation", "JEJUNAL PERFORATION", "PERFORATION JEJUNAL", "jejunum; perforation", "Perforation of jejunum", "perforation of jejunum", "Perforation of jejunum (disorder)", "perforation of jejunum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perforation of jejunum", "shortest_name_length": 19}
{"curie": "MONDO:0800096", "names": ["osteomalacia", "disorder of bone mineralization", "abnormal mineralization disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "abnormal mineralization disorder", "shortest_name_length": 12}
{"curie": "UMLS:C0039980", "names": ["CHEST INJURY", "Chest injury", "chest injury", "trauma chest", "Chest Injury", "chest trauma", "Injury, Chest", "injury thorax", "thorax; wound", "chest traumas", "wound; thorax", "chest injuries", "thorax; injury", "injury; thorax", "Chest Injuries", "injuries chest", "injury thoracic", "Injury-Thoracic", "Thoracic Injury", "thoracic injury", "injuries thorax", "Injuries, Chest", "thorax injuries", "Injury, Thoracic", "Injury to Thorax", "injury of thorax", "thoracic injuries", "Thoracic Injuries", "Injuries, Thoracic", "Injuries to the thorax", "Chest injury (disorder)", "chest disorders injuries", "Traumatic injury to chest", "Traumatic chest injury NOS", "Chest Injuries and Disorders", "injury of thorax (diagnosis)", "Unspecified injury of thorax", "Injuries to the thorax (S20-S29)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thoracic Injuries", "shortest_name_length": 12}
{"curie": "UMLS:C1279270", "names": ["Lambda light chain myeloma", "Lambda Light Chain Myeloma", "Lambda Light Chain Multiple Myeloma", "Lambda light chain myeloma (disorder)", "Lambda light chain myeloma (diagnosis)", "malignant neoplasm multiple myeloma lambda light chain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lambda light chain myeloma", "shortest_name_length": 26}
{"curie": "UMLS:C0729520", "names": ["Bacterial lower respiratory infection", "Bacterial lower respiratory infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bacterial lower respiratory infection", "shortest_name_length": 37}
{"curie": "MONDO:0008315", "names": ["prostate ca", "Prostate cancer", "PROSTATE CANCER", "Prostate Cancer", "prostate cancer", "Prostate Cancers", "Prostate--Cancer", "Prostatic cancer", "Cancer, Prostate", "prostatic cancer", "Prostatic Cancer", "Cancer, Prostatic", "prostate neoplasm", "Cancers, Prostate", "Prostatic Cancers", "Cancers, Prostatic", "prostatic neoplasm", "Cancer of Prostate", "Cancer of prostate", "cancer of prostate", "Prostatic Neoplasms", "Prostate cancer NOS", "tumor of the prostate", "prostate gland cancer", "cancer of the prostate", "Cancer of the Prostate", "CA - Cancer of prostate", "Neoplasm malig;prostate", "malignant prostate tumor", "cancer of prostate gland", "Malignant Prostate Tumor", "Malignant prostatic tumor", "prostate cancer, familial", "Malignant prostatic tumour", "hereditary prostate cancer", "Malignant neoplasm prostate", "Malignant tumor of prostate", "malignant tumor of prostate", "malignant prostate neoplasm", "prostate cancer (diagnosis)", "Malignant Tumor of Prostate", "Malignant Prostate Neoplasm", "Malignant tumour of prostate", "NGP - new growth of prostate", "Prostatic neoplasms malignant", "Malignant Neoplasm of Prostate", "malignant neoplasm of prostate", "Malignant neoplasm of prostate", "malignant tumor of the prostate", "Malignant Tumor of the Prostate", "malignant prostate gland neoplasm", "prostate gland neoplasm malignant", "Malignant Neoplasm of the Prostate", "malignant neoplasm of the prostate", "malignant neosplasm of the prostate", "malignant neoplasm of prostate gland", "Malignant tumor of prostate (disorder)", "malignant neoplasm of prostate gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate cancer", "shortest_name_length": 11}
{"curie": "MONDO:0100125", "names": ["hallucinogen-persisting perception disorder", "hallucinogen abuse with hallucinogen persisting perception disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hallucinogen-persisting perception disorder", "shortest_name_length": 43}
{"curie": "MONDO:0044704", "names": ["Oropharyngeal Epidermoid Carcinoma", "epidermoid carcinoma of oropharynx", "Epidermoid Carcinoma of Oropharynx", "oropharyngeal epidermoid carcinoma", "oropharynx squamous cell carcinoma", "Cancer of oropharynx, squamous cell", "epidermoid carcinoma, oropharyngeal", "Squamous cell carcinoma of oropharynx", "Oropharyngeal squamous cell carcinoma", "Oropharyngeal Squamous Cell Carcinoma", "Squamous Cell Carcinoma of Oropharynx", "oropharyngeal squamous cell carcinoma", "squamous cell carcinoma of oropharynx", "epidermoid carcinoma of the oropharynx", "squamous cell carcinoma, oropharyngeal", "Epidermoid Carcinoma of the Oropharynx", "Oropharyngeal Throat Squamous Cell Cancer", "squamous cell carcinoma of the oropharynx", "Squamous Cell Carcinoma of the Oropharynx", "Squamous cell carcinoma of the oropharynx", "oropharyngeal throat squamous cell cancer", "primary squamous cell carcinoma of oropharynx", "Primary squamous cell carcinoma of oropharynx", "Squamous cell carcinoma of oropharynx (disorder)", "squamous cell carcinoma of oropharynx (diagnosis)", "Primary squamous cell carcinoma of oropharynx (disorder)", "primary squamous cell carcinoma of oropharynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oropharynx squamous cell carcinoma", "shortest_name_length": 34}
{"curie": "UMLS:C4721796", "names": ["FIGO Stage IIIC Ovarian Cancer", "FIGO Stage IIIC Ovarian Carcinoma", "stage IIIC ovarian epithelial cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Stage IIIC Ovarian Cancer", "shortest_name_length": 30}
{"curie": "MONDO:0017262", "names": ["isolated inherited ichthyosis", "nonsyndromic inherited ichthyosis", "inherited non-syndromic ichthyosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited non-syndromic ichthyosis", "shortest_name_length": 29}
{"curie": "UMLS:C0027531", "names": ["Injury;neck", "Neck Injury", "Neck injury", "neck injury", "NECK INJURY", "neck; injury", "injury; neck", "Injury, Neck", "Neck Injuries", "neck injuries", "Injuries, Neck", "Injury of neck", "injury of neck", "Neck injury NOS", "Injuries to the neck", "injuries to the neck", "Injury of neck (disorder)", "injury of neck (diagnosis)", "Unspecified injury of neck", "Injuries to the neck (S10-S19)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neck Injuries", "shortest_name_length": 11}
{"curie": "MONDO:0056799", "names": ["synovium disorder", "Synovial disorder", "Synovial disorders", "disorder of synovium", "Disorder of synovium", "Synovial disorder NOS", "Disorder of synovium, NOS", "Synovial membrane abnormal", "disease (or disorder); synovium", "Disorder of synovium (disorder)", "layer of synovial tissue disease", "disease of layer of synovial tissue", "disorder of layer of synovial tissue", "layer of synovial tissue disease or disorder", "disease or disorder of layer of synovial tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "synovium disorder", "shortest_name_length": 17}
{"curie": "UMLS:C4727798", "names": ["Relapsed FLC", "Recurrent FLC", "Relapsed Fibrolamellar Carcinoma", "Recurrent Fibrolamellar Carcinoma", "Relapsed Fibrolamellar Hepatocellular Carcinoma", "Recurrent Fibrolamellar Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Fibrolamellar Carcinoma", "shortest_name_length": 12}
{"curie": "UMLS:C1709977", "names": ["Rupture Of Hyaloid Face"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rupture Of Hyaloid Face", "shortest_name_length": 23}
{"curie": "MONDO:0017249", "names": ["CPAM type 1", "CCAM type 1", "congenital cystic disease of the lung type 1", "congenital pulmonary airway malformation type 1", "congenital cystic adenomatoid malformation of the lung type 1", "congenital cystic adenomatous malformation of the lung type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital pulmonary airway malformation type 1", "shortest_name_length": 11}
{"curie": "UMLS:C4687631", "names": ["Recurrent Central Nervous System Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Central Nervous System Non-Hodgkin Lymphoma", "shortest_name_length": 53}
{"curie": "UMLS:C3898123", "names": ["Nonerosive Arthritis", "Non-Erosive Arthritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nonerosive Arthritis", "shortest_name_length": 20}
{"curie": "MONDO:0015814", "names": ["PCFCL", "Crosti's disease", "Crosti's Disease", "Crosti's lymphoma", "cutaneous follicle center lymphoma", "Reticulohistiocytoma of the dorsum", "Cutaneous Follicle Centre Lymphoma", "Reticulohistiocytoma of the Dorsum", "cutaneous follicle centre lymphoma", "Cutaneous Follicle Center Lymphoma", "primary cutaneous follicle center lymphoma", "Primary Cutaneous Follicle Center Lymphoma", "Primary cutaneous follicle center lymphoma", "Primary cutaneous follicle centre lymphoma", "Primary cutaneous follicle center cell lymphoma", "Primary cutaneous follicle centre cell lymphoma", "Primary cutaneous follicular center B-cell lymphoma", "Primary cutaneous follicular centre B-cell lymphoma", "Primary cutaneous follicle centre-cell B-cell lymphoma", "Primary cutaneous follicular center B-cell lymphoma (disorder)", "Primary cutaneous follicular center B-cell lymphoma (diagnosis)", "Primary cutaneous follicle center cell lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary cutaneous follicle center lymphoma", "shortest_name_length": 5}
{"curie": "MONDO:0100215", "names": ["RILDBC", "RILDBC1", "NEDBLLA", "RAJAB SYNDROME", "Rajab syndrome", "NEDBLLA, FORMERLY", "Brain calcification Rajab type", "brain calcification, Rajab type", "Brain calcification, Rajab type", "Brain calcification Rajab type (disorder)", "RAJAB INTERSTITIAL LUNG DISEASE WITH BRAIN CALCIFICATIONS", "RAJAB INTERSTITIAL LUNG DISEASE WITH BRAIN CALCIFICATIONS 1", "Rajab interstitial lung disease with brain calcifications 1", "neurodevelopmental disorder with brain, liver, and lung abnormalities", "developmental delay, small stature, microcephaly, and brain calcifications", "NEURODEVELOPMENTAL DISORDER WITH BRAIN, LIVER, AND LUNG ABNORMALITIES, FORMERLY", "DEVELOPMENTAL DELAY, SMALL STATURE, MICROCEPHALY, AND BRAIN CALCIFICATIONS, FORMERLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rajab interstitial lung disease with brain calcifications 1", "shortest_name_length": 6}
{"curie": "UMLS:C1709248", "names": ["Non-Neoplastic Disease by Special Category", "Non-Neoplastic Disorder by Special Category"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Disorder by Special Category", "shortest_name_length": 42}
{"curie": "UMLS:C2987141", "names": ["Pancreatic Poorly Differentiated Ductal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Poorly Differentiated Ductal Adenocarcinoma", "shortest_name_length": 54}
{"curie": "MONDO:0025382", "names": ["Rous sarcoma", "avian sarcoma", "Avian Sarcoma", "sarcoma, Rous", "Avian sarcoma", "Sarcoma, Avian", "Avian Sarcomas", "Avian sarcomas", "sarcoma, avian", "Sarcomas, Avian", "sarcomas, Avian", "Avian sarcoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sarcoma, avian", "shortest_name_length": 12}
{"curie": "MONDO:0016007", "names": ["cocaine fetopathy", "fetal cocaine syndrome", "Fetal cocaine syndrome", "cocaine fetal syndrome", "cocaine embryofetopathy", "Cocaine embryofetopathy", "Foetal cocaine syndrome", "prenatal cocaine exposure", "cocaine antenatal exposure", "Fetal cocaine syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cocaine embryofetopathy", "shortest_name_length": 17}
{"curie": "UMLS:C1334024", "names": ["High Risk Esophageal GIST", "High Risk Esophageal Gastrointestinal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Risk Esophageal Gastrointestinal Stromal Tumor", "shortest_name_length": 25}
{"curie": "UMLS:C4331333", "names": ["Stage IV Lip and Oral Cavity Cancer", "Stage IV Lip and Oral Cavity Cancer AJCC v8", "Stage IV Lip and Oral Cavity Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Lip and Oral Cavity Cancer AJCC v8", "shortest_name_length": 35}
{"curie": "UMLS:C5555181", "names": ["Refractory Ovarian Low Grade Serous Adenocarcinoma", "Refractory Low Grade Ovarian Serous Adenocarcinoma", "Refractory Ovarian-Low Grade Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Ovarian Low Grade Serous Adenocarcinoma", "shortest_name_length": 50}
{"curie": "MONDO:0022971", "names": ["diabetes persistent mullerian ducts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diabetes persistent mullerian ducts", "shortest_name_length": 35}
{"curie": "MONDO:0021643", "names": ["MESENTERIC VARIX", "Mesenteric varices", "mesenteric varices", "Varicose mesenteric vein", "mesentery varicose disease", "varicose disease of mesentery", "Venous ectasia of mesenteric vein", "Venous ectasia of mesenteric vein (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mesenteric varices", "shortest_name_length": 16}
{"curie": "MONDO:0002000", "names": ["anaerobic meningitis", "Anaerobic meningitis", "Meningitis anaerobic bacterial NOS", "Meningitis due to anaerobic bacteria", "meningitis due to anaerobic bacteria", "Meningitis caused by anaerobic bacteria", "meningitis caused by anaerobic bacteria", "meningitis due to anaerobic bacteria (diagnosis)", "Meningitis caused by anaerobic bacteria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anaerobic meningitis", "shortest_name_length": 20}
{"curie": "MONDO:0007220", "names": ["BDB", "BDB1", "Type B brachydactyly", "Brachydactyly, Type B", "BRACHYDACTYLY, TYPE B", "brachydactyly, type B", "brachydactyly type B1", "Brachydactyly type B1", "brachydactyly, type B1", "BRACHYDACTYLY, TYPE B1", "Brachydactyly, Type B1", "ROR2 brachydactyly type B", "brachydactyly type B caused by mutation in ROR2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly type B1", "shortest_name_length": 3}
{"curie": "UMLS:C0269192", "names": ["CERVICAL ATYPIA", "Cervical Atypia", "cervical atypism", "Cervical atypism", "CERVICAL ATYPISM", "Cervical Atypism", "Cervical atypism (disorder)", "cervical atypism (diagnosis)", "Cellular Cervical Abnormality", "dysplasia of cervix (uteri) cervical atypism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical atypism", "shortest_name_length": 15}
{"curie": "UMLS:C1336342", "names": ["Laryngeal Cancer Stage IVA", "stage IVA laryngeal cancer", "Stage IVA Larynx Carcinoma", "Stage IVA Laryngeal Cancer", "Stage IVA Carcinoma of Larynx", "Stage IVA Laryngeal Carcinoma", "Stage IVA Laryngeal Throat Cancer", "Stage IVA Carcinoma of the Larynx", "Stage IVA Laryngeal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Laryngeal Cancer AJCC v7", "shortest_name_length": 26}
{"curie": "OMIM:129150", "names": ["E11S", "Echo Virus 11 Sensitivity", "ECHO VIRUS 11 SENSITIVITY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 4}
{"curie": "MONDO:0035349", "names": ["localized DEB", "localized dystrophic epidermolysis bullosa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "localized dystrophic epidermolysis bullosa", "shortest_name_length": 13}
{"curie": "MONDO:0013408", "names": ["IMD90", "FADD DEFICIENCY", "Fadd deficiency", "FADD-related immunodeficiency", "FADD (FAS-associated protein with death domain) related immunodeficiency", "Immunodeficiency due to mutation of FAS-associated protein with death domain gene", "IMMUNODEFICIENCY 90 WITH ENCEPHALOPATHY, FUNCTIONAL HYPOSPLENIA, AND HEPATIC DYSFUNCTION", "immunodeficiency 90 with encephalopathy, functional hyposplenia, and hepatic dysfunction", "Immunodeficiency due to mutation of FAS-associated protein with death domain gene (disorder)", "infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovascular malformations", "INFECTIONS, RECURRENT, WITH ENCEPHALOPATHY, HEPATIC DYSFUNCTION, AND CARDIOVASCULAR MALFORMATIONS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FADD-related immunodeficiency", "shortest_name_length": 5}
{"curie": "UMLS:C0346353", "names": ["Orbit Hemangiopericytoma", "Orbital Hemangiopericytoma", "Hemangiopericytoma of Orbit", "hemangiopericytoma of orbit", "Hemangiopericytoma of orbit", "Haemangiopericytoma of orbit", "Hemangiopericytoma of the Orbit", "benign neoplasm hemangiopericytoma", "Hemangiopericytoma of orbit (disorder)", "hemangiopericytoma of orbit (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemangiopericytoma of orbit", "shortest_name_length": 24}
{"curie": "MONDO:0035449", "names": ["atelencephaly", "atelencephalic microcephaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atelencephaly", "shortest_name_length": 13}
{"curie": "MONDO:0001451", "names": ["Peripheral retinal degeneration", "Peripheral Retinal Degeneration", "peripheral retinal Degeneration", "peripheral retinal degeneration", "Peripheral retinal degenerations", "retina; degeneration, peripheral", "degeneration; retina, peripheral", "Peripheral degeneration of retina", "peripheral degeneration of retina", "Peripheral retinal degeneration, NOS", "Peripheral retinal degeneration (disorder)", "Unspecified peripheral retinal degeneration", "peripheral retinal degeneration (diagnosis)", "Peripheral retinal degeneration, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peripheral retinal degeneration", "shortest_name_length": 31}
{"curie": "MONDO:0008246", "names": ["PPRCA", "PPCRA", "PIGMENTED PARAVENOUS CHORIORETINAL ATROPHY", "pigmented paravenous chorioretinal atrophy", "Pigmented paravenous chorioretinal atrophy", "Pigmented Paravenous Chorioretinal Atrophy", "pigmented paravenous retinochoroidal atrophy", "Pigmented paravenous retinochoroidal atrophy", "PPRCA - pigmented paravenous retinochoroidal atrophy", "Pigmented paravenous retinochoroidal atrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pigmented paravenous retinochoroidal atrophy", "shortest_name_length": 5}
{"curie": "UMLS:C0854144", "names": ["Septic arthritis streptobacillus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Septic arthritis streptobacillus", "shortest_name_length": 32}
{"curie": "MONDO:0016807", "names": ["Pure mitochondrial myopathy", "pure mitochondrial myopathy", "Pure mitochondrial myopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pure mitochondrial myopathy", "shortest_name_length": 27}
{"curie": "MONDO:0037252", "names": ["thecoma", "Thecoma", "THECOMA", "Thecomas", "thecomas", "Thecoma NOS", "Fibrothecoma", "Thecoma, NOS", "theca cell tumor", "Theca cell tumor", "Theca Cell Tumor", "Tumor, Theca Cell", "Theca cell tumour", "theca cell; tumor", "tumor; theca cell", "Theca Cell Tumors", "Tumors, Theca Cell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thecoma", "shortest_name_length": 7}
{"curie": "UMLS:C2700000", "names": ["Physical Entrapment"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Physical Entrapment", "shortest_name_length": 19}
{"curie": "UMLS:C0234936", "names": ["Application site edema", "EDEMA APPLICATION SITE", "Edema application site", "APPLICATION SITE EDEMA", "APPLICATION SITE OEDEMA", "Application site oedema", "Oedema application site", "Edema at application site", "Oedema at application site", "application site disorder edema", "Application site edema (disorder)", "Application site edema (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Application site edema", "shortest_name_length": 22}
{"curie": "MONDO:0011045", "names": ["MMEP", "MCOPS8", "MMEP syndrome", "Viljoen Smart syndrome", "Viljoen-Smart syndrome", "microphthalmia syndromic 8", "syndromic microphthalmia 8", "Microphthalmia, syndromic 8", "MICROPHTHALMIA, SYNDROMIC 8", "microphthalmia, syndromic 8", "Syndromic microphthalmia type 8", "syndromic microphthalmia type 8", "microcephaly microphthalmia ectrodactyly of lower limbs and prognathism", "microcephaly, microphthalmia, ectrodactyly of Lower limbs, and prognathism", "Microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism", "MICROCEPHALY, MICROPHTHALMIA, ECTRODACTYLY OF LOWER LIMBS, AND PROGNATHISM", "microcephaly-microphthalmia-ectrodactyly of lower limbs-prognathism syndrome", "Microcephaly-microphthalmia-ectrodactyly of lower limbs-prognathism syndrome", "Microcephaly, microphthalmia, ectrodactyly of lower limbs and prognathism syndrome", "Microcephaly, microphthalmia, ectrodactyly of lower limbs and prognathism syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MMEP syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0154558", "names": ["Endocrine Disorder Arising from Mental Factor", "Endocrine disorder arising from mental factors"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endocrine disorder arising from mental factors", "shortest_name_length": 45}
{"curie": "MONDO:0030045", "names": ["LIBF", "SEMDLIBF", "Liberfarb syndrome", "LIBERFARB SYNDROME", "spondyloepimetaphyseal dysplasia, Liberfarb Type", "SPONDYLOEPIMETAPHYSEAL DYSPLASIA, LIBERFARB TYPE", "Short stature-skeletal dysplasia-retinal degeneration-intellectual disability-sensorineural hearing loss syndrome", "short stature-skeletal dysplasia-retinal degeneration-intellectual disability-sensorineural hearing loss syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liberfarb syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0012680", "names": ["NPHP7", "Nephronophthisis 7", "NEPHRONOPHTHISIS 7", "nephronophthisis 7", "nephronophthisis type 7", "GLIS2 nephronophthisis (disease)", "nephronophthisis (disease) caused by mutation in GLIS2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephronophthisis 7", "shortest_name_length": 5}
{"curie": "MONDO:0002221", "names": ["urethra urothelial papilloma", "urethral urothelial papilloma", "Urethral Urothelial Papilloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urethral urothelial papilloma", "shortest_name_length": 28}
{"curie": "MONDO:0021056", "names": ["FAP1", "BTPS2", "Gardner syndrome", "adenomatous polyposis coli", "adenoma, periampullary, somatic", "ADENOMA, PERIAMPULLARY, SOMATIC", "familial polyposis of the colon", "brain tumor-polyposis syndrome 2", "BRAIN TUMOR-POLYPOSIS SYNDROME 2", "Brain Tumor-Polyposis Syndrome 2", "familial adenomatous polyposis 1", "Adenomatous Intestinal Polyposes", "Adenomatous Intestinal Polyposis", "Intestinal Polyposis, Adenomatous", "Polyposis, Adenomatous Intestinal", "POLYPOSIS, ADENOMATOUS INTESTINAL", "polyposis, adenomatous intestinal", "adenomatous polyposis of the colon", "adenomatous polyposis coli, attenuated", "familial adenomatous polyposis, attenuated", "BRAIN TUMOR-POLYPOSIS SYNDROME 2 (disorder)", "APC attenuated familial adenomatous polyposis", "attenuated familial adenomatous polyposis caused by mutation in APC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial adenomatous polyposis 1", "shortest_name_length": 4}
{"curie": "MONDO:0014729", "names": ["SPG75", "hereditary spastic paraplegia 75", "MAG hereditary spastic paraplegia", "hereditary spastic paraplegia type 75", "autosomal recessive spastic paraplegia 75", "SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE", "spastic paraplegia 75, autosomal recessive", "autosomal recessive spastic paraplegia type 75", "Autosomal recessive spastic paraplegia type 75", "hereditary spastic paraplegia caused by mutation in MAG", "Autosomal recessive spastic paraplegia type 75 (disorder)", "autosomal recessive spastic paraplegia type 75 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 75", "shortest_name_length": 5}
{"curie": "UMLS:C5419807", "names": ["Small HCC", "Small Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Hepatocellular Carcinoma", "shortest_name_length": 9}
{"curie": "MONDO:0002639", "names": ["IX Nerve Disorder", "IX nerve disorder", "ninth nerve disorder", "Ninth Nerve Disorder", "Disorder of ninth nerve", "Cranial Nerve IX Diseases", "Cranial Nerve IX Disorders", "Disorder of cranial nerve 9", "ninth cranial nerve disease", "Ninth Cranial Nerve Diseases", "Ninth cranial nerve disorder", "n.glossopharyngeus; disorder", "Glossopharyngeal nerve lesion", "Glossopharyngeal Nerve Disease", "Disorder of IXth cranial nerve", "glossopharyngeal nerve disease", "Glossopharyngeal Nerve Diseases", "glossopharyngeal nerve disorder", "Glossopharyngeal nerve disorder", "disorder glossopharyngeal nerve", "Glossopharyngeal Nerve Disorder", "Glossopharyngeal nerve disorders", "Disorders of other cranial nerves", "disease of glossopharyngeal nerve", "disorder of glossopharyngeal nerve", "Disorder of glossopharyngeal nerve", "Disorder of the ninth cranial nerve", "Disorders of glossopharyngeal nerve", "Glossopharyngeal nerve disorder NOS", "Ninth cranial nerve disease or syndrome", "Glossopharyngeal nerve disease or syndrome", "glossopharyngeal nerve disease or disorder", "Disorder of glossopharyngeal nerve (disorder)", "disease or disorder of glossopharyngeal nerve", "disease (or disorder); nerve, glossopharyngeal", "disorder of glossopharyngeal nerve (diagnosis)", "cranial nerve; disorder, ninth (glossopharyngeal)", "disease (or disorder); cranial nerve, ninth (glossopharyngeal)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glossopharyngeal nerve disorder", "shortest_name_length": 17}
{"curie": "MONDO:0011014", "names": ["PPB", "Pleuropulmonary blastoma", "pleuropulmonary blastoma", "Pleuropulmonary Blastoma", "childhood pulmonary blastoma", "pediatric pulmonary blastoma", "Pulmonary Blastoma of Childhood", "pulmonary blastoma of childhood", "PPB familial tumor and dysplasia syndrome", "pleuropulmonary blastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pleuropulmonary blastoma", "shortest_name_length": 3}
{"curie": "MONDO:0019427", "names": ["X-linked neurodegenerative syndrome Bertini type", "X-linked neurodegenerative syndrome, Bertini type", "X-linked neurodegenerative syndrome Bertini type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked neurodegenerative syndrome, Bertini type", "shortest_name_length": 48}
{"curie": "MONDO:0019728", "names": ["HCDD", "Heavy chain deposition disease", "Heavy Chain Deposition Disease", "heavy chain deposition disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heavy chain deposition disease", "shortest_name_length": 4}
{"curie": "UMLS:C0969687", "names": ["Autosomal Chromosome Disorder", "Autosomal Chromosome Disorders", "Autosomal chromosomal disorder", "Chromosome Disorder, Autosomal", "Chromosome Disorders, Autosomal", "Autosomal chromosomal abnormalities", "Autosomal chromosomal disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Autosomal Chromosome Disorders", "shortest_name_length": 29}
{"curie": "MONDO:0007178", "names": ["aurocephalosyndactyly", "AUROCEPHALOSYNDACTYLY", "Aurocephalosyndactyly", "AURALCEPHALOSYNDACTYLY", "Auralcephalosyndactyly", "aural cephalosyndactyly", "Kurczynski-Casperson syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aurocephalosyndactyly", "shortest_name_length": 21}
{"curie": "MONDO:0016904", "names": ["partial deletion of chromosome 5q", "partial monosomy of chromosome 5q", "partial monosomy of the long arm of chromosome 5", "partial deletion of the long arm of chromosome 5", "partial deletion of the long arm of chromosome type 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of the long arm of chromosome 5", "shortest_name_length": 33}
{"curie": "MONDO:0002874", "names": ["testicular Pure germ cell tumor", "testicular pure germ cell tumor", "Testicular Pure Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular pure germ cell tumor", "shortest_name_length": 31}
{"curie": "UMLS:C0745527", "names": ["Klebsiella bacteremia", "KLEBSIELLA BACTEREMIA", "Klebsiella bacteraemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Klebsiella bacteremia", "shortest_name_length": 21}
{"curie": "MONDO:0006527", "names": ["anidrosis", "Anhidrosis", "ANHYDROSIS", "anhydrosis", "anhidrosis", "ANHIDROSIS", "Anhydrosis", "adiaphoresis", "Adiaphoresis", "absent sweating", "Absent sweating", "SWEATING ABSENCE", "Sweating, absent", "Lack of sweating", "absence of sweating", "Absence of sweating", "Sweating dysfunction", "Anhidrosis (disorder)", "Sudomotor dysfunction", "anhidrosis (diagnosis)", "anhidrosis (physical finding)", "Absence of sweating (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anhidrosis", "shortest_name_length": 9}
{"curie": "MONDO:0020048", "names": ["Internal carotid absence", "internal carotid agenesis", "internal carotid artery agenesis", "Internal carotid artery agenesis", "Agenesis of internal carotid artery", "agenesis of the internal carotid artery", "Agenesis of internal carotid artery (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "internal carotid agenesis", "shortest_name_length": 24}
{"curie": "MONDO:0100442", "names": ["RP2", "RP2 retinopathy", "retinitis pigmentosa 2", "RP2-related retinopathy", "RP2 retinitis pigmentosa", "retinitis pigmentosa type 2", "retinitis pigmentosa caused by mutation in RP2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "RP2-related retinopathy", "shortest_name_length": 3}
{"curie": "UMLS:C1699211", "names": ["Intraoperative ear injury", "intraoperative ear injury", "Intraoperative Ear Injury", "intraoperative ear injury (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraoperative Ear Injury", "shortest_name_length": 25}
{"curie": "UMLS:C4727365", "names": ["Recurrent Paget Disease of the Anal Canal", "Recurrent Paget's Disease of the Anal Canal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Paget Disease of the Anal Canal", "shortest_name_length": 41}
{"curie": "MONDO:0006593", "names": ["pelvic lipomatosis", "Pelvic Lipomatosis", "Pelvic lipomatosis", "pelvic lipomatosis (morphologic abnormality)", "Pelvic lipomatosis (morphologic abnormality)", "Excess of mature unencapsulated fatty tissue in the pelvis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pelvic lipomatosis", "shortest_name_length": 18}
{"curie": "MONDO:0045044", "names": ["Desmopathy", "ligament disorder", "Ligament disorder", "ligament; disorder", "ligament disorders", "Ligament disorders", "disease of ligament", "disorder of ligament", "Disorder of ligament", "Ligament disorder NOS", "Ligamentous Disorders", "Disorder of ligament, NOS", "ligament disease or disorder", "Disorder of ligament (disorder)", "disease or disorder of ligament", "disorder of ligament (diagnosis)", "Disorder of ligament, site unspecified", "Disorder of ligament, unspecified site", "disease (or disorder); ligament, ligament"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ligament disorder", "shortest_name_length": 10}
{"curie": "UMLS:C4526909", "names": ["Uterine Corpus Sarcoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Corpus Sarcoma by AJCC v7 Stage", "shortest_name_length": 39}
{"curie": "UMLS:C0155003", "names": ["Blindness;temporary", "BLINDNESS TEMPORARY", "transient blindness", "Blindness temporary", "temporary blindness", "Blindness transient", "Transient Blindness", "BLINDNESS TRANSIENT", "Transient blindness", "transient; blindness", "Blindness, Transient", "blindness; transient", "temporary vision loss", "Transient visual loss", "transient visual loss", "loss temporary vision", "Temporary vision loss", "Transient blindness, NOS", "Transient blindness (disorder)", "Transient visual loss (disorder)", "transient visual loss (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Blindness, Transient", "shortest_name_length": 19}
{"curie": "MONDO:0022020", "names": ["Boudhina Yedes Khiari syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Boudhina Yedes Khiari syndrome", "shortest_name_length": 30}
{"curie": "MONDO:0020500", "names": ["MHF", "marburg disease", "Marburg disease", "Marburg Disease", "Disease, Marburg", "green monkey disease", "Green monkey disease", "marburg virus disease", "MARBURG VIRUS DISEASE", "Vervet monkey disease", "Marburg virus disease", "Marburg Virus Disease", "Marburg virus infection", "Marburg Hemorrhagic Fever", "Marburg hemorrhagic fever", "Fever, Marburg Hemorrhagic", "Marburg haemorrhagic fever", "Hemorrhagic Fever, Marburg", "GREEN MONKEY VIRUS DISEASE", "Marburg viral hemorrhagic fever", "Marburg viral haemorrhagic fever", "Marburg virus disease (disorder)", "Viral hemorrhagic fever, Marburg", "Marburg virus disease (diagnosis)", "Viral haemorrhagic fever, Marburg"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Marburg hemorrhagic fever", "shortest_name_length": 3}
{"curie": "UMLS:C0546125", "names": ["Mild nemaline myopathy", "Childhood-onset nemaline myopathy", "Childhood Onset Nemaline Myopathy", "Nemaline Myopathy, Childhood Onset", "Nemaline myopathy, childhood onset", "Childhood-onset nemaline myopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nemaline Myopathy, Childhood Onset", "shortest_name_length": 22}
{"curie": "MONDO:0002286", "names": ["RENOVASCULAR", "renovascular", "Renal Artery Disease", "renal artery disease", "Renal vessel disorder", "RENAL VESSEL DISORDER", "Renal vascular disease", "vascular renal disease", "renal vascular disease", "Renal vascular disorder", "Renal Vascular Disorder", "Kidney Vascular Disorder", "RENAL VASCULAR DISORDERS", "Renal vascular disorder NOS", "vascular disorder of kidney", "Vascular disorder of kidney", "Vascular disorders of kidney", "Renal vascular disorder, NOS", "Renal vascular disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal artery disease", "shortest_name_length": 12}
{"curie": "MONDO:0011826", "names": ["FGD2", "FGD1", "GCCD2", "GCCD1", "ACTH resistance", "ACTH Resistance", "ACTH RESISTANCE", "ACTH Receptor Defect", "Glucocorticoid Deficiency 1", "GLUCOCORTICOID DEFICIENCY 2", "Glucocorticoid Deficiency 2", "GLUCOCORTICOID DEFICIENCY 1", "glucocorticoid deficiency 2", "glucocorticoid deficiency type 2", "Adrenal Unresponsiveness to ACTH", "ADRENAL UNRESPONSIVENESS TO ACTH", "FAMILIAL GLUCOCORTICOID DEFICIENCY 1", "Familial Glucocorticoid Deficiency 2", "Familial Glucocorticoid Deficiency 1", "familial glucocorticoid deficiency 2", "FAMILIAL GLUCOCORTICOID DEFICIENCY 2", "MRAP familial glucocorticoid deficiency", "Familial Glucocorticoid Deficiency Type 1", "Familial Glucocorticoid Deficiency Type 2", "Melanocortin-2 Receptor Accessory Protein Defect", "familial glucocorticoid deficiency caused by mutation in MRAP"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glucocorticoid deficiency 2", "shortest_name_length": 4}
{"curie": "MONDO:0009149", "names": ["ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome", "ectodermal dysplasia, hypohidrotic, with hypothyroidism and agenesis of the corpus callosum", "Ectodermal Dysplasia, Hypohidrotic, with Hypothyroidism and Agenesis of the Corpus Callosum", "ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH HYPOTHYROIDISM AND AGENESIS OF THE CORPUS CALLOSUM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome", "shortest_name_length": 89}
{"curie": "UMLS:C0151947", "names": ["THROMBOSIS PULMONARY ARTERY", "PULMONARY ARTERY THROMBOSIS", "Thrombosis pulmonary artery", "Pulmonary artery thrombosis", "THROMBOSIS, PULMONARY ARTERY", "Thrombus of pulmonary artery", "Pulmonary arterial thrombosis", "thrombosis of pulmonary artery", "Pulmonary artery thrombosis (disorder)", "thrombosis of pulmonary artery (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pulmonary artery thrombosis", "shortest_name_length": 27}
{"curie": "MONDO:0014568", "names": ["SPG73", "hereditary spastic paraplegia 73", "hereditary spastic paraplegia type 73", "autosomal dominant spastic paraplegia 73", "SPASTIC PARAPLEGIA 73, AUTOSOMAL DOMINANT", "spastic paraplegia 73, autosomal dominant", "autosomal dominant spastic paraplegia type 73", "Autosomal dominant spastic paraplegia type 73", "CPT1C autosomal dominant pure spastic paraplegia", "Autosomal dominant spastic paraplegia type 73 (disorder)", "autosomal dominant spastic paraplegia type 73 (diagnosis)", "autosomal dominant pure spastic paraplegia caused by mutation in CPT1C"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 73", "shortest_name_length": 5}
{"curie": "MONDO:0021034", "names": ["genetic alopecia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genetic alopecia", "shortest_name_length": 16}
{"curie": "MONDO:0006385", "names": ["PIOSCC", "Primary Intraosseous Carcinoma, NOS", "primary intraosseous squamous cell carcinoma", "Primary Intraosseous Squamous Cell Carcinoma", "Primary Intraosseous Carcinoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary intraosseous squamous cell carcinoma", "shortest_name_length": 6}
{"curie": "UMLS:C1335360", "names": ["Parotid Lipoma", "Lipoma of Parotid", "Parotid Gland Lipoma", "Lipoma of the Parotid", "Lipoma of Parotid Gland", "Lipoma of the Parotid Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parotid Gland Lipoma", "shortest_name_length": 14}
{"curie": "MONDO:0011061", "names": ["CHOREA, REMITTING, WITH NYSTAGMUS AND CATARACT", "Chorea, Remitting, with Nystagmus and Cataract", "chorea, remitting, with nystagmus and cataract", "Chorea, remitting with nystagmus and cataracts", "chorea, remitting with nystagmus and cataracts", "familial remitting chorea, nystagmus and cataracts", "Familial remitting chorea, nystagmus and cataracts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chorea, remitting, with nystagmus and cataract", "shortest_name_length": 46}
{"curie": "MONDO:0012355", "names": ["DFNB28", "autosomal recessive deafness 28", "deafness, autosomal recessive 28", "DEAFNESS, AUTOSOMAL RECESSIVE 28", "Deafness, Autosomal Recessive 28", "deafness, autosomal recessive type 28", "autosomal recessive nonsyndromic deafness 28", "autosomal recessive nonsyndromic hearing loss 28", "TRIOBP autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic deafness type 28", "autosomal recessive nonsyndromic deafness caused by mutation in TRIOBP"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 28", "shortest_name_length": 6}
{"curie": "MONDO:0005742", "names": ["Pneumocholecystitis", "Gaseous cholecystitis", "gaseous pericholecystitis", "Gaseous pericholecystitis", "Emphysematous Cholecystitis", "emphysematous cholecystitis", "Emphysematous cholecystitis", "cholecystitis; emphysematous", "emphysematous; cholecystitis", "Cholecystitis, Emphysematous", "Pneumocholecystitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "emphysematous cholecystitis", "shortest_name_length": 19}
{"curie": "MONDO:0014935", "names": ["FMD2", "FRONTOMETAPHYSEAL DYSPLASIA 2", "Frontometaphyseal dysplasia 2", "frontometaphyseal dysplasia 2", "Frontometaphyseal dysplasia type 2", "MAP3K7 frontometaphyseal dysplasia", "frontometaphyseal dysplasia 2; FMD2", "frontometaphyseal dysplasia caused by mutation in MAP3K7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontometaphyseal dysplasia 2", "shortest_name_length": 4}
{"curie": "MONDO:0001670", "names": ["Tooth Resorption", "Tooth resorption", "tooth resorption", "resorption tooth", "Tooth Resorptions", "teeth; resorption", "Resorption, Tooth", "resorption; tooth", "Resorptions, Tooth", "pathological resorption", "Pathological tooth resorption", "Pathological resorption of teeth", "pathological resorption of tooth", "Pathological resorption of tooth", "Pathological resorption of tooth, NOS", "pathological resorption of dental structure", "Pathological resorption of tooth (disorder)", "pathological resorption of tooth (diagnosis)", "pathological resorption of dental structure (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tooth resorption", "shortest_name_length": 16}
{"curie": "MONDO:0004445", "names": ["bladder papillary clear cell adenocarcinoma", "Bladder Papillary Clear Cell Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder papillary clear cell adenocarcinoma", "shortest_name_length": 43}
{"curie": "UMLS:C1322281", "names": ["Seasonal Rhinitis", "Seasonal rhinitis", "Rhinitis seasonal", "seasonal rhinitis", "Hayfever/allergic rhinitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rhinitis seasonal", "shortest_name_length": 17}
{"curie": "MONDO:0011955", "names": ["T2D4", "Niddm4", "NIDDM4", "TYPE 2 DIABETES MELLITUS 4", "Noninsulin-Dependent Diabetes Mellitus 4", "noninsulin-dependent diabetes mellitus 4", "NONINSULIN-DEPENDENT DIABETES MELLITUS 4", "diabetes mellitus, noninsulin-dependent, 4", "DIABETES MELLITUS, NONINSULIN-DEPENDENT, 4", "Diabetes Mellitus, Noninsulin-Dependent, Type 4", "diabetes mellitus, noninsulin-dependent, type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diabetes mellitus, noninsulin-dependent, 4", "shortest_name_length": 4}
{"curie": "MONDO:0009549", "names": ["Stgd", "EOSRD", "STGD1", "SECORD", "Stargardt disease 1", "fundus flavimaculatus", "Stargardt disease type 1", "Juvenile macular degeneration", "Juvenile Macular Degeneration", "Juvenile Macular Degenerations", "MACULAR DEGENERATION, JUVENILE", "Degeneration, Juvenile Macular", "Macular Degeneration, Juvenile", "macular Degeneration, juvenile", "Early-onset severe retinal dystrophy", "early-onset severe retinal dystrophy", "RETINAL DYSTROPHY, EARLY-ONSET SEVERE", "retinal dystrophy, early-onset severe", "Retinal dystrophy, severe early-onset", "Retinal Dystrophy, Early Onset Severe", "macular dystrophy with flecks, type 1", "Severe early-childhood-onset retinal dystrophy", "Severe early childhood onset retinal dystrophy", "severe early-childhood-onset retinal dystrophy", "SECORD - Severe early childhood onset retinal dystrophy", "Severe early childhood onset retinal dystrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe early-childhood-onset retinal dystrophy", "shortest_name_length": 4}
{"curie": "MONDO:0043085", "names": ["Mosaic trisomy 1q12 q21", "uniparental disomy 1q12 q21", "Uniparental disomy 1q12 q21", "Chromosome 1, uniparental disomy 1q12 q21", "chromosome 1, uniparental disomy 1q12 q21"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 1, uniparental disomy 1q12 q21", "shortest_name_length": 23}
{"curie": "UMLS:C2825742", "names": ["Disseminated JXG", "Disseminated Juvenile Xanthogranuloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disseminated Juvenile Xanthogranuloma", "shortest_name_length": 16}
{"curie": "MONDO:0022607", "names": ["vagina Brenner tumor", "Brenner tumor of the vagina", "extraovarian Brenner tumor of the vagina"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extraovarian Brenner tumor of the vagina", "shortest_name_length": 20}
{"curie": "UMLS:C0278498", "names": ["Gastric cancer stage IV", "Stage IV Gastric Cancer", "stage IV gastric cancer", "gastric cancer stage IV", "gastric cancer, stage IV", "stomach cancer, stage IV", "metastatic stomach cancer", "Metastatic gastric cancer", "metastatic gastric cancer", "stomach cancer, metastatic", "gastric cancer, metastatic", "Gastric cancer stage IV NOS", "Stomach cancer stage IV NOS", "Stage IV Gastric Cancer AJCC v7", "Gastric malignancy stage IV NOS", "Stage IV Gastric (Stomach) Cancer", "malignant tumor of stomach stage IV", "Malignant neoplasm of stomach stage IV", "malignant neoplasm of stomach stage IV", "Malignant neoplasm of stomach stage IV NOS", "malignant neoplasm of stomach stage IV (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant neoplasm of stomach stage IV", "shortest_name_length": 23}
{"curie": "MONDO:0009584", "names": ["Mutchinick Syndrome", "Mutchinick syndrome", "MUTCHINICK SYNDROME", "mental retardation Buenos Aires type", "Buenos Aires type mental retardation", "Mental Retardation, Buenos Aires Type", "mental retardation, Buenos Aires type", "MENTAL RETARDATION, BUENOS AIRES TYPE", "intellectual deficit Buenos-Aires type", "Intellectual disability Buenos Aires type", "intellectual disability Buenos Aires type", "intellectual disability, Buenos Aires type", "intellectual disability, Buenos-Aires type", "Intellectual disability, Buenos Aires type", "Intellectual disability, Buenos-Aires type", "Intellectual disability Buenos Aires type (disorder)", "Intellectual disability, Buenos Aires type (diagnosis)", "mental retardation-microcephaly-blepharochalasis syndrome", "mental and physical retardation-speech disorders-peculiar facies syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, Buenos-Aires type", "shortest_name_length": 19}
{"curie": "MONDO:0019036", "names": ["amoebiasis due to free-living amoebae"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amoebiasis due to free-living amoebae", "shortest_name_length": 37}
{"curie": "UMLS:C3640092", "names": ["Venous Thrombosis due to Vascular Access Complication", "Venous Thrombosis Related to Vascular Access Complication", "Acquired Secondary Venous Thrombosis due to Catheter Complication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Venous Thrombosis Related to Vascular Access Complication", "shortest_name_length": 53}
{"curie": "MONDO:0009579", "names": ["FTHS", "TER HAAR SYNDROME", "ter Haar syndrome", "Ter Haar syndrome", "Frank-Ter Haar syndrome", "FRANK-TER HAAR SYNDROME", "FRANK-TER Haar syndrome", "Frank-Ter Haar Syndrome", "Frank Ter Haar syndrome", "Borrone Di Rocco Crovato syndrome", "Borrone di Rocco Crovato syndrome", "Frank-Ter Haar syndrome (disorder)", "BORRONE DERMATOCARDIOSKELETAL SYNDROME", "Borrone dermatocardioskeletal syndrome", "Borrone Dermatocardioskeletal syndrome", "[OBSOLETE] Borrone Di Rocco Crovato syndrome", "autosomal recessive Melnick-Needles syndrome", "Melnick-Needles syndrome, autosomal recessive", "MELNICK-NEEDLES SYNDROME, AUTOSOMAL RECESSIVE, FORMERLY", "autosomal recessive Melnick-Needles syndrome (formerly)", "Melnick-Needles syndrome, autosomal recessive, formerly", "megalocornea, multiple skeletal anomalies, and developmental delay", "Megalocornea, multiple skeletal anomalies, and developmental delay"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Frank-Ter Haar syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0007560", "names": ["Reading seizure", "reading seizures", "Reading Epilepsy", "reading epilepsy", "Seizure, reading", "Reading epilepsy", "Reading seizures", "EPILEPSY, READING", "Epilepsy, Reading", "epilepsy, reading", "Epilepsy, reading", "Reading Epilepsies", "Epilepsies, Reading", "Reading Reflex Epilepsy", "Reflex Epilepsy, Reading", "Epilepsy, Reading Reflex", "Reading seizure (finding)", "Reading Reflex Epilepsies", "Reflex Epilepsies, Reading", "Epilepsies, Reading Reflex"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "reading seizures", "shortest_name_length": 15}
{"curie": "MONDO:0001159", "names": ["personality split", "Split Personality", "split personality", "personalities split", "personality multiple", "Multiple personality", "Multiple Personality", "multiple personality", "Personality, Multiple", "personality; multiple", "multiple; personality", "Multiple Personalities", "multiple personalities", "Personalities, Multiple", "multiple identity disorder", "Multiple Identity Disorder", "Disorder, Multiple Identity", "Identity Disorder, Multiple", "Multiple Identity Disorders", "PERSONALITY DISORDER MULTIPLE", "Multiple personality disorder", "Multiple Personality Disorder", "disorder multiple personality", "multiple personality disorder", "personality disorder multiple", "multiple personality; disorder", "multiple personality disorders", "disorder; multiple personality", "Dissociative Identity Disorder", "Dissociative identity disorder", "personality disorder; multiple", "Personality Disorder, Multiple", "Multiple Personality Disorders", "dissociative identity disorder", "multiple; personality disorder", "identity dissociative disorder", "dissociative identify disorder", "disorder dissociative identity", "Disorder, Multiple Personality", "Personality Disorders, Multiple", "dissociative; identity disorder", "disorder multiple personalities", "disorders dissociative identity", "Disorder, Dissociative Identity", "Identity Disorder, Dissociative", "identity disorder; dissociative", "identity; disorder, dissociative", "disorder; identity, dissociative", "disorders multiple personalities", "Multiple personality disorder (disorder)", "dissociative identity disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple personality disorder", "shortest_name_length": 17}
{"curie": "MONDO:0016615", "names": ["oligoarticular JIA with anti-nuclear antibodies", "pauciarticular chronic arthritis with anti-nuclear antibodies", "oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies", "shortest_name_length": 47}
{"curie": "MONDO:0007136", "names": ["anorectal anomalies", "genetic anorectal anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genetic anorectal anomalies", "shortest_name_length": 19}
{"curie": "UMLS:C0393546", "names": ["Oculopharyngeal spinal muscular atrophy", "Oculopharyngeal Spinal Muscular Atrophy", "Spinal Muscular Atrophy, Oculopharyngeal", "Oculopharyngeal spinal muscular atrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oculopharyngeal Spinal Muscular Atrophy", "shortest_name_length": 39}
{"curie": "MONDO:0011488", "names": ["MCPH3", "primary autosomal recessive microcephaly 3", "Microcephaly, Primary Autosomal Recessive, 3", "MICROCEPHALY 3, PRIMARY, AUTOSOMAL RECESSIVE", "microcephaly 3, primary, autosomal recessive", "CDK5RAP2 autosomal recessive primary microcephaly", "autosomal recessive primary microcephaly caused by mutation in CDK5RAP2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly 3, primary, autosomal recessive", "shortest_name_length": 5}
{"curie": "UMLS:C1333848", "names": ["Grade 3a Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade 3a Malignant Neoplasm", "shortest_name_length": 27}
{"curie": "MONDO:0033259", "names": ["DFNA72", "deafness, autosomal dominant 72", "DEAFNESS, AUTOSOMAL DOMINANT 72", "hearing loss, autosomal dominant 72", "autosomal dominant nonsyndromic deafness 72"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal dominant 72", "shortest_name_length": 6}
{"curie": "MONDO:0016526", "names": ["trisomy 9p", "9p trisomy", "Trisomy 9p", "9p syndrome", "9p+ syndrome", "9p duplication", "Duplication 9p", "trisomy type 9p", "Rethore syndrome", "Réthoré syndrome", "dup(9p) syndrome", "partial trisomy 9p", "Trisomy 9p partial", "Trisomy 9p syndrome", "chromosome 9p trisomy", "Duplication 9p partial", "9p duplication syndrome", "duplication 9p syndrome", "chromosome 9p duplication", "9p partial trisomy syndrome", "Chromosome 9, partial trisomy 9p", "partial trisomy of chromosome 9p", "chromosome 9p duplication syndrome", "partial duplication of chromosome 9p", "9p partial trisomy syndrome (disorder)", "9p partial trisomy syndrome (diagnosis)", "trisomy of the short arm of chromosome 9", "Trisomy of the short arm of chromosome 9", "Duplication of the short arm of chromosome 9", "partial trisomy of the short arm of chromosome 9", "partial duplication of the short arm of chromosome 9", "partial trisomy of the short arm of chromosome type 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trisomy 9p", "shortest_name_length": 10}
{"curie": "UMLS:C2981276", "names": ["Stage IVA Thyroid Gland Anaplastic Carcinoma AJCC v7", "Undifferentiated (Anaplastic) Stage IVA Thyroid Gland Cancer", "Stage IVA Thyroid Gland Undifferentiated (Anaplastic) Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Thyroid Gland Undifferentiated (Anaplastic) Carcinoma AJCC v7", "shortest_name_length": 52}
{"curie": "UMLS:C0854894", "names": ["Relapsed Angiosarcoma", "Recurrent Angiosarcoma", "Angiosarcoma recurrent", "Relapsed Hemangiosarcoma", "Recurrent Hemangiosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Angiosarcoma recurrent", "shortest_name_length": 21}
{"curie": "MONDO:0006327", "names": ["Eye Sebaceous Carcinoma", "eye sebaceous carcinoma", "Ocular Sebaceous Carcinoma", "ocular sebaceous carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ocular sebaceous carcinoma", "shortest_name_length": 23}
{"curie": "MONDO:0024520", "names": ["RHDA3", "renal hypodysplasia/aplasia 3", "RENAL HYPODYSPLASIA/APLASIA 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal hypodysplasia/aplasia 3", "shortest_name_length": 5}
{"curie": "UMLS:C4744393", "names": ["Sellar Immature Teratoma", "Immature Teratoma of the Sellar Region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sellar Immature Teratoma", "shortest_name_length": 24}
{"curie": "UMLS:C0495499", "names": ["Atresia or stricture of auditory canal", "Atresia or stricture of external auditory canal", "Congenital absence, atresia and stricture of auditory canal (external)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital absence, atresia and stricture of auditory canal (external)", "shortest_name_length": 38}
{"curie": "MONDO:0014642", "names": ["CANDF9", "candidiasis, familial, 9", "CANDIDIASIS, FAMILIAL, 9", "candidiasis, familial, type 9", "IL17RC chronic mucocutaneous candidiasis (disease)", "chronic mucocutaneous candidiasis (disease) caused by mutation in IL17RC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "candidiasis, familial, 9", "shortest_name_length": 6}
{"curie": "UMLS:C4552923", "names": ["Stage IB Fallopian Tube Cancer", "Stage IB Fallopian Tube Cancer AJCC v8", "Stage IB Fallopian Tube Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Fallopian Tube Cancer AJCC v8", "shortest_name_length": 30}
{"curie": "UMLS:C1332284", "names": ["Anaplastic Lymphoma PTLD", "Anaplastic Diffuse Large B-Cell Lymphoma PTLD", "Anaplastic Lymphoma Post-Transplant Lymphoproliferative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anaplastic Lymphoma Post-Transplant Lymphoproliferative Disorder", "shortest_name_length": 24}
{"curie": "MONDO:0009899", "names": ["POLYHYDRAMNIOS, CHRONIC IDIOPATHIC", "Polyhydramnios, Chronic Idiopathic", "polyhydramnios, chronic idiopathic", "Lactogen Receptor Defect of Chorion", "Lactogen receptor defect of chorion", "LACTOGEN RECEPTOR DEFECT OF CHORION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyhydramnios, chronic idiopathic", "shortest_name_length": 34}
{"curie": "MONDO:0041996", "names": ["thallium poison", "Thallium poisoning", "thallium poisoning", "THALLIUM POISONING", "poisoning by thallium", "Thallium poisoning syndrome", "Thallium poisoning (disorder)", "poisoning by thallium (diagnosis)", "Thallium or thallium compound causing toxic effect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thallium poisoning", "shortest_name_length": 15}
{"curie": "MONDO:0043919", "names": ["radiation fibrosis", "RADIATION PNEUMONIA", "Radiation Pneumonia", "radiation pneumonia", "fibrosis, radiation", "Pneumonia, Radiation", "pneumonia; radiation", "radiation Pneumonias", "pneumonia, radiation", "radiation; pneumonia", "Radiation Pneumonitis", "radiation pneumonitis", "PNEUMONITIS RADIATION", "Radiation pneumonitis", "Pneumonias, radiation", "RADIATION PNEUMONITIS", "pneumonitis, radiation", "PNEUMONITIS, RADIATION", "pneumonitis; radiation", "pneumonitis radiations", "radiation; pneumonitis", "Pneumonitis, Radiation", "radiation Pneumonitides", "Pneumonitides, radiation", "Radiation-Induced Pneumonitis", "pulmonary radiation alveolitis", "Pulmonary radiation alveolitis", "Radiation pneumonitis (disorder)", "radiation pneumonitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radiation pneumonitis", "shortest_name_length": 18}
{"curie": "UMLS:C4683239", "names": ["Pathologic Stage III Retinoblastoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage III Retinoblastoma AJCC v8", "shortest_name_length": 43}
{"curie": "UMLS:C1997142", "names": ["Organic FTT", "Organic Failure to Thrive", "Organic failure to thrive", "organic failure to thrive", "OFTT - Organic failure to thrive", "Organic failure to thrive (disorder)", "organic failure to thrive (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Organic failure to thrive", "shortest_name_length": 11}
{"curie": "MONDO:0011053", "names": ["NBs", "NBS", "NCBRS", "SMARCA2-related BAFopathy", "Nicolaides-Baraitser Syndrome", "NICOLAIDES-BARAITSER SYNDROME", "NICOLAIDES-Baraitser syndrome", "Nicolaides Baraitser syndrome", "Nicolaides-Baraitser syndrome", "sparse hair and mental retardation", "SPARSE HAIR AND MENTAL RETARDATION", "Sparse hair and mental retardation", "sparse hair and intellectual disability", "Nicolaides-Baraitser syndrome (disorder)", "intellectual disability-sparse hair-brachydactyly syndrome", "Intellectual disability-sparse hair-brachydactyly syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability-sparse hair-brachydactyly syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0005377", "names": ["Nephrosis", "nephrosis", "Syndrome nephrotic", "SYNDROME NEPHROTIC", "nephrotic syndrome", "Nephrotic Syndrome", "Nephrotic syndrome", "NEPHROTIC SYNDROME", "syndrome, nephrotic", "Syndrome, Nephrotic", "syndrome; nephrotic", "nephrotic syndromes", "nephrotic; syndrome", "Nephrotic Syndromes", "syndromes, nephrotic", "NS - Nephrotic syndrome", "Nephrotic syndrome, NOS", "Nephrotic syndrome (disorder)", "nephrotic syndrome (diagnosis)", "Nephrotic syndrome, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrotic syndrome", "shortest_name_length": 9}
{"curie": "MONDO:0000732", "names": ["combined oxidative phosphorylation deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation deficiency", "shortest_name_length": 45}
{"curie": "MONDO:0007002", "names": ["IVth nerve disorder", "Trochlear Neuropathy", "Neuropathy, Trochlear", "Trochlear Neuropathies", "trochlear nerve disease", "Neuropathies, Trochlear", "Trochlear Nerve Disease", "Trochlear Nerve Diseases", "disorder trochlear nerve", "Trochlear nerve disorder", "trochlear nerve disorder", "Trochlear Nerve Disorder", "Trochlear Nerve Disorders", "Cranial Nerve IV Diseases", "Superior Oblique Myokymia", "Superior oblique myokymia", "Myokymia, Superior Oblique", "disease of trochlear nerve", "Superior Oblique Myokymias", "IVth Cranial Nerve Disorder", "Disorder of trochlear nerve", "disorder of trochlear nerve", "Myokymias, Superior Oblique", "IVth cranial nerve disorder", "Trochlear nerve disease, NOS", "Fourth Cranial Nerve Diseases", "Trochlear nerve disorder, NOS", "Fourth cranial nerve disorder", "Fourth cranial nerve disease, NOS", "Neurogenic Superior Oblique Palsy", "Fourth cranial nerve disorder, NOS", "Superior Oblique Palsy, Neurogenic", "trochlear nerve disease or disorder", "Trochlear nerve disease or syndrome", "Superior oblique myokymia (disorder)", "disease or disorder of trochlear nerve", "disease (or disorder); trochlear nerve", "Disorder of trochlear nerve (diagnosis)", "Fourth cranial nerve disease or syndrome", "Superior oblique muscle innervation disorder", "superior oblique muscle innervation disorder", "disease (or disorder); cranial nerve, fourth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trochlear nerve disorder", "shortest_name_length": 19}
{"curie": "MONDO:0030531", "names": ["SPGF65", "SPERMATOGENIC FAILURE 65", "spermatogenic failure 65"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 65", "shortest_name_length": 6}
{"curie": "MONDO:0019887", "names": ["Trisomy 16qter", "trisomy 16qter", "distal trisomy 16q", "Distal trisomy 16q", "distal duplication 16q", "Distal duplication 16q", "distal trisomy type 16q", "Telomeric duplication 16q", "telomeric duplication 16q", "Distal trisomy 16q (disorder)", "Distal trisomy 16q (diagnosis)", "anomaly of chromosome pair 16 partial trisomy 16q distal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal trisomy 16q", "shortest_name_length": 14}
{"curie": "UMLS:C5237442", "names": ["Resectable Lung Non-Small Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Lung Non-Small Cell Carcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0008215", "names": ["ADLD", "Multiple Sclerosis-Like Disorder", "multiple sclerosis-like disorder", "Adult onset autosomal dominant leukodystrophy", "adult-onset autosomal dominant leukodystrophy", "Adult onset autosomal dominant leucodystrophy", "Adult-onset autosomal dominant leukodystrophy", "LEUKODYSTROPHY, ADULT-ONSET, AUTOSOMAL DOMINANT", "leukodystrophy, adult-onset, autosomal dominant", "autosomal dominant leukodystrophy with autonomic disease", "Adult onset autosomal dominant leukodystrophy (disorder)", "autosomal dominant adult-onset demyelinating leukodystrophy", "Adult-onset autosomal dominant demyelinating leukodystrophy", "adult-onset autosomal dominant demyelinating leukodystrophy", "leukodystrophy, demyelinating, ADULT-onset, autosomal dominant", "Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant", "LEUKODYSTROPHY, DEMYELINATING, ADULT-ONSET, AUTOSOMAL DOMINANT", "autosomal-dominant or late-onset type Pelizaeus-Merzbacher disease", "Pelizaeus-Merzbacher disease, autosomal dominant or late-onset type", "Pelizaeus-Merzbacher Disease, Autosomal Dominant Or Late-Onset Type", "PELIZAEUS-MERZBACHER DISEASE, AUTOSOMAL DOMINANT OR LATE-ONSET TYPE, FORMERLY", "Pelizaeus-Merzbacher disease, autosomal dominant or late-onset type, formerly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult-onset autosomal dominant demyelinating leukodystrophy", "shortest_name_length": 4}
{"curie": "MONDO:0004358", "names": ["Subglottic Cancer", "subglottic cancer", "Cancer of Subglottis", "cancer of subglottis", "Subglottic Carcinoma", "subglottic carcinoma", "Subglottic carcinoma", "Subglottis Carcinoma", "subglottis carcinoma", "Carcinoma of subglottis", "carcinoma of subglottis", "Carcinoma of Subglottis", "Cancer of the Subglottis", "subglottic throat cancer", "cancer of the subglottis", "Subglottic Throat Cancer", "carcinoma of the subglottis", "Carcinoma of the Subglottis", "Carcinoma of subglottis (disorder)", "Carcinoma of subglottis (diagnosis)", "malignant subglottis neoplasm carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subglottis carcinoma", "shortest_name_length": 17}
{"curie": "MONDO:0007215", "names": ["BDA1", "brachydactyly type A1", "Brachydactyly type A1", "Type A1 brachydactyly", "brachydactyly, type A1", "Brachydactyly, type A1", "BRACHYDACTYLY, TYPE A1", "Brachydactyly, Type A1", "Brachydactyly Farabee type", "Farabee-Type Brachydactyly", "FARABEE-TYPE BRACHYDACTYLY", "Farabee-type brachydactyly", "Farabee type brachydactyly", "brachydactyly Farabee type", "Brachydactyly, Farabee type", "brachydactyly, Farabee type", "Brachydactyly type A1 (disorder)", "BRACHYDACTYLY, TYPE A1 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly type A1", "shortest_name_length": 4}
{"curie": "MONDO:0016521", "names": ["Hoffman syndrome", "Kocher-Debré-Semelaigne syndrome", "Kocher-Debre-Semelaigne syndrome", "muscular pseudohypertrophy-hypothyroidism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular pseudohypertrophy-hypothyroidism syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0020356", "names": ["Cat eye", "Keyhole iris", "notch of iris", "Iris coloboma", "iris; coloboma", "Coloboma, iris", "coloboma; iris", "coloboma iridis", "Coloboma of iris", "Coloboma of Iris", "coloboma of iris", "Coloboma of the Iris", "coloboma of the iris", "Coloboma of the iris", "coloboma of iris (disease)", "coloboma iridis (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coloboma of iris", "shortest_name_length": 7}
{"curie": "MONDO:0005386", "names": ["PAD", "pad", "Chronic limb ischemia", "Chronic limb ischaemia", "Peripheral Artery Disease", "peripheral artery disease", "Peripheral Arterial Disease", "peripheral arterial disease", "peripheral arterial disorder", "Peripheral Arterial Disorder", "Peripheral artery occlusive disease", "Peripheral obliterative arteriopathy", "Peripheral arterial occlusive disease", "Peripheral Arterial Occlusive Disease", "peripheral arterial occlusive disease", "PAOD - Peripheral arterial occlusive disease", "Peripheral arterial occlusive disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peripheral arterial disease", "shortest_name_length": 3}
{"curie": "MONDO:0010007", "names": ["SAO PAULO MCA/MR SYNDROME", "Sao Paulo MCA/MR syndrome", "sao Paulo MCA/Mr syndrome", "Sao Paulo MCA-MR Syndrome", "microbrachycephaly ptosis cleft lip", "RICHIERI-COSTA/GUION-ALMEIDA SYNDROME", "Richieri-COSTA/Guion-Almeida syndrome", "Richieri Costa-Guion Almeida-Ramos syndrome", "microbrachycephaly-ptosis-cleft lip syndrome", "SHORT STATURE, MENTAL RETARDATION, EYE ANOMALIES, AND CLEFT LIP/PALATE", "short stature, mental retardation, eye anomalies, and cleft Lip/palate", "short stature, intellectual disability, eye anomalies, and cleft Lip/palate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microbrachycephaly-ptosis-cleft lip syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0021575", "names": ["OOMD4", "oocyte maturation defect 4", "Oocyte Maturation Defect-4", "OOCYTE MATURATION DEFECT 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oocyte maturation defect 4", "shortest_name_length": 5}
{"curie": "UMLS:C4287589", "names": ["STIC", "Serous Tubal Intraepithelial Carcinoma", "Serous tubal intraepithelial carcinoma", "Serous tubal intraepithelial carcinoma (STIC)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Serous Tubal Intraepithelial Carcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0008012", "names": ["MONOPHALANGY OF GREAT TOE", "Monophalangy of Great Toe", "Monophalangy of great toe"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Monophalangy of great toe", "shortest_name_length": 25}
{"curie": "MONDO:0700014", "names": ["chromosome 7 disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 7 disorder", "shortest_name_length": 21}
{"curie": "UMLS:C1709838", "names": ["Rare Non-Neoplastic Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rare Non-Neoplastic Disorder", "shortest_name_length": 28}
{"curie": "UMLS:C4763508", "names": ["Familial Adrenal Gland Pheochromocytoma", "Hereditary Adrenal Gland Pheochromocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Familial Adrenal Gland Pheochromocytoma", "shortest_name_length": 39}
{"curie": "MONDO:0018122", "names": ["digital anomalies-intellectual disability-short stature syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "digital anomalies-intellectual disability-short stature syndrome", "shortest_name_length": 64}
{"curie": "UMLS:C1334048", "names": ["HPV-Related Adenocarcinoma", "Human Papillomavirus-Related Adenocarcinoma", "Human Papilloma Virus Related Adenocarcinoma", "Human Papilloma Virus-Related Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Human Papillomavirus-Related Adenocarcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0017410", "names": ["Porencephaly", "porencephaly", "Porencephalies", "porencephalic cyst", "Porencephalic cyst", "Porencephalic Cyst", "cysts porencephalic", "porencephalic; cyst", "Cavity within brain", "cyst; porencephalic", "Familial porencephaly", "Posttraumatic Porencephaly", "Post-traumatic Porencephaly", "Post traumatic Porencephaly", "Post-traumatic porencephaly", "Familial porencephalic cyst", "Porencephaly, Posttraumatic", "Porencephaly, Post-traumatic", "Posttraumatic Porencephalies", "Post-traumatic Porencephalies", "Encephaloclastic Porencephaly", "Porencephalies, Posttraumatic", "Porencephalic cyst (disorder)", "Porencephalies, Post-traumatic", "Porencephaly, Encephaloclastic", "porencephalic cyst (diagnosis)", "Familial porencephaly (disorder)", "Post-traumatic porencephalic cyst", "Posttraumatic porencephalic cyst of brain", "Posttraumatic porencephalic cyst of brain (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "porencephaly", "shortest_name_length": 12}
{"curie": "UMLS:C1336311", "names": ["Stage II Paranasal Sinus Cancer", "Paranasal Sinus Cancer Stage II", "Stage II Accessory Sinus Carcinoma", "Stage II Paranasal Sinus Carcinoma", "Stage II Carcinoma of Paranasal Sinus", "Stage II Carcinoma of Accessory Sinus", "Stage II Paranasal Sinus Cancer AJCC v6", "Stage II Paranasal Sinus Cancer AJCC v7", "Stage II Carcinoma of the Accessory Sinus", "Stage II Carcinoma of the Paranasal Sinus", "Stage II Paranasal Sinus Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Paranasal Sinus Cancer AJCC v6 and v7", "shortest_name_length": 31}
{"curie": "MONDO:0021638", "names": ["Astrocytoma low grade", "Low-Grade Astrocytoma", "astrocytoma low grade", "low grade astrocytoma", "Low-grade astrocytoma", "Low Grade Astrocytoma", "Astrocytoma, low grade", "Low Grade Astrocytic Tumor", "low-grade astrocytic tumor", "low grade astrocytic tumor", "Low-Grade Astrocytic Tumor", "low grade astrocytic neoplasm", "Low-Grade Astrocytic Neoplasm", "low-grade astrocytic neoplasm", "Low Grade Astrocytic Neoplasm", "low grade astrocytoma (diagnosis)", "Astrocytoma low grade (morphologic abnormality)", "brain tumor malignant astrocytoma grades I & II low grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "low grade astrocytic tumor", "shortest_name_length": 21}
{"curie": "UMLS:C0029944", "names": ["OVERDOSE", "overdose", "Overdose", "overdoses", "Overdose NOS", "drug overdose", "Overdose, NOS", "Drug overdose", "Drug Overdose", "DRUG OVERDOSE", "drug overdoses", "Drug Overdoses", "Overdose, Drug", "Overdose, drug", "Overdoses, Drug", "Drugs--Overdose", "Overdose of drug", "Drug overdose, NOS", "OD - Overdose of drug"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drug Overdose", "shortest_name_length": 8}
{"curie": "MONDO:0006034", "names": ["STAS", "stomach adenosquamous carcinoma", "Gastric Adenosquamous Carcinoma", "gastric adenosquamous carcinoma", "adenosquamous carcinoma of stomach", "Adenosquamous Carcinoma of Stomach", "Adenosquamous carcinoma of stomach", "gastric (stomach) adenosquamous cancer", "adenosquamous carcinoma of the stomach", "Gastric (Stomach) Adenosquamous Cancer", "Adenosquamous Carcinoma of the Stomach", "adenosquamous carcinoma of stomach (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric adenosquamous carcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0003357", "names": ["Lung Leiomyosarcoma", "lung leiomyosarcoma", "Leiomyosarcoma of Lung", "leiomyosarcoma of lung", "Pulmonary Leiomyosarcoma", "pulmonary leiomyosarcoma", "leiomyosarcoma of the lung", "Leiomyosarcoma of the Lung", "leiomyosarcoma of lung (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung leiomyosarcoma", "shortest_name_length": 19}
{"curie": "UMLS:C1405500", "names": ["uvea; prolapse", "Uveal prolapse", "Uveal Prolapse", "prolapse; uveal", "Prolapse of uvea", "Uveal prolapse (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uveal prolapse", "shortest_name_length": 14}
{"curie": "MONDO:0034872", "names": ["large granular lymphocyte leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "large granular lymphocyte leukemia", "shortest_name_length": 34}
{"curie": "UMLS:C0278785", "names": ["relapsed adult ALL", "Relapsed Adult ALL", "Recurrent Adult ALL", "relapsed ALL, adult", "recurrent adult ALL", "ALL, relapsed, adult", "recurrent ALL, adult", "ALL, recurrent, adult", "Relapsed Adult Acute Lymphoid Leukemia", "Recurrent Adult Acute Lymphoid Leukemia", "relapsed adult acute lymphocytic leukemia", "Relapsed Adult Acute Lymphocytic Leukemia", "adult acute lymphocytic leukemia, relapsed", "leukemia, relapsed adult acute lymphocytic", "lymphocytic leukemia, relapsed adult acute", "Recurrent Adult Acute Lymphocytic Leukemia", "recurrent adult acute lymphocytic leukemia", "Relapsed Adult Acute Lymphogenous Leukemia", "Recurrent Adult Acute Lymphogenous Leukemia", "acute lymphocytic leukemia, relapsed, adult", "Relapsed Adult Acute Lymphoblastic Leukemia", "recurrent adult acute lymphoblastic leukemia", "acute lymphocytic leukemia, recurrent, adult", "Recurrent Acute Lymphoblastic Leukemia (ALL)", "Recurrent Adult Acute Lymphoblastic Leukemia", "Recurrent Adult Precursor Lymphoblastic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Adult Acute Lymphoblastic Leukemia", "shortest_name_length": 18}
{"curie": "EFO:1002021", "names": ["ankle injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ankle injury", "shortest_name_length": 12}
{"curie": "UMLS:C5670664", "names": ["Intracranial Mesenchymal Tumor with FET-CREB Fusion", "Intracranial Mesenchymal Tumor, FET-CREB Fusion-Positive", "Intracranial Mesenchymal Tumor, FET::CREB Fusion-Positive", "Intracranial Mesenchymal Tumor /Angiomatoid Fibrous Histiocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intracranial Mesenchymal Tumor, FET-CREB Fusion-Positive", "shortest_name_length": 51}
{"curie": "UMLS:C0008087", "names": ["Child Nutrition Disorder", "Nutrition Disorder, Child", "Child Nutrition Disorders", "Nutrition Disorders, Child", "Nutrition disorders in children"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Child Nutrition Disorders", "shortest_name_length": 24}
{"curie": "MONDO:0005712", "names": ["nystagmus", "Nystagmus congenital", "Congenital nystagmus", "congenital nystagmus", "Congenital Nystagmus", "NYSTAGMUS CONGENITAL", "Nystagmus, Congenital", "nystagmus, congenital", "NYSTAGMUS, CONGENITAL", "Nystagmus, congenital", "motor congenital nystagmus", "congenital pathologic nystagmus", "congenital idiopathic nystagmus", "Congenital nystagmus (disorder)", "congenital nystagmus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital nystagmus", "shortest_name_length": 9}
{"curie": "UMLS:C4525723", "names": ["Nuclear Cataract Grade 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nuclear Cataract Grade 1", "shortest_name_length": 24}
{"curie": "UMLS:C0685125", "names": ["Benign Great Vessel Tumor", "Benign Great Vessel Neoplasm", "Benign Tumor of Great Vessel", "Benign Neoplasm of Great Vessel", "Benign Tumor of the Great Vessel", "Benign neoplasm of great vessels", "Benign Neoplasm of the Great Vessel", "Benign neoplasm of great vessels (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign neoplasm of great vessels", "shortest_name_length": 25}
{"curie": "UMLS:C0544688", "names": ["complication disease", "Disease complication", "disease complication", "complications disease", "complications diseases", "complication of disease", "Complication of disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disease complication", "shortest_name_length": 20}
{"curie": "MONDO:0019353", "names": ["FFM", "STGD", "STGD1", "Stargardt", "Stargardt 1", "Stargardt disease", "Stargardt Disease", "STARGARDT DISEASE", "STARGARDT SYNDROME", "Stargardt Disease 1", "Stargardt disease-1", "Stargardt's disease", "Stargardt disease 1", "STARGARDT DISEASE 1", "stargardt's disease", "FUNDUS FLAVIMACULATUS", "Fundus flavimaculatus", "fundus flavimaculatus", "Fundus Flavimaculatus", "FFM - Fundus flavimaculatus", "Stargardt macular dystrophy", "Stargardt disease (diagnosis)", "Stargardt macular degeneration", "Stargardt Macular Degeneration", "STARGARDT DISEASE 1 (disorder)", "Stargardt's disease (disorder)", "Stargardt disease-1 (diagnosis)", "Macular Degeneration, Stargardt", "Stargardt Macular Degenerations", "Degeneration, Stargardt Macular", "Fundus flavimaculatus (disorder)", "fundus flavimaculatus (diagnosis)", "juvenile onset macular degeneration", "MACULAR DYSTROPHY WITH FLECKS, TYPE 1", "Macular Dystrophy With Flecks, Type 1", "Familial juvenile macular degeneration syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stargardt disease", "shortest_name_length": 3}
{"curie": "MONDO:0015514", "names": ["Stunting", "Stuntings", "Stunted Growth", "growth disorder", "Growth Disorder", "Growth, Stunted", "Growth disorder", "Growth disorders", "Disorder, Growth", "growth disorders", "Growth Disorders", "disorders growth", "disorder; growth", "genetic endocrine growth disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genetic endocrine growth disease", "shortest_name_length": 8}
{"curie": "UMLS:C1377630", "names": ["Adenocarcinoma in situ in a polyp", "Adenocarcinoma In Situ in a Polyp", "Adenocarcinoma in situ in a polyp, NOS", "Adenocarcinoma in situ in a polyp (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma in situ in a polyp", "shortest_name_length": 33}
{"curie": "MONDO:0800001", "names": ["DSPD", "DELAYED SLEEP PHASE DISORDER, SUSCEPTIBILITY TO", "delayed sleep phase syndrome, susceptibility to", "delayed sleep phase disorder, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "delayed sleep phase syndrome, susceptibility to", "shortest_name_length": 4}
{"curie": "MONDO:0022909", "names": ["cutis laxa osteoporosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutis laxa osteoporosis", "shortest_name_length": 23}
{"curie": "UMLS:C2931118", "names": ["Interstitial megalocytic nephritis", "Megalocytic interstitial nephritis", "Transplant megalocytic interstitial nephritis (type)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Megalocytic interstitial nephritis", "shortest_name_length": 34}
{"curie": "MONDO:0013104", "names": ["BCC4", "basal cell carcinoma, susceptibility to, 4", "BASAL CELL CARCINOMA, SUSCEPTIBILITY TO, 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "basal cell carcinoma, susceptibility to, 4", "shortest_name_length": 4}
{"curie": "UMLS:C3496069", "names": ["cocaine use", "cocaine use (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cocaine use", "shortest_name_length": 11}
{"curie": "UMLS:C0277919", "names": ["Venous Stasis Syndrome", "Venous stasis syndrome", "Syndrome, Venous Stasis", "Postthrombotic Syndrome", "Postthrombotic syndrome", "postthrombotic syndrome", "Post thrombotic syndrome", "Syndrome, Postthrombotic", "post thrombotic syndrome", "Postthrombotic syndrome NOS", "Venous stasis syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postthrombotic Syndrome", "shortest_name_length": 22}
{"curie": "MONDO:0011369", "names": ["FH3", "Fh3", "FHCL3", "LDLCQ1", "HCHOLA3", "hypercholesterolemia, familial, 3", "HYPERCHOLESTEROLEMIA, FAMILIAL, 3", "PCSK9 familial hypercholesterolemia", "HYPERCHOLESTEROLEMIA, AUTOSOMAL DOMINANT, 3", "Hypercholesterolemia, Autosomal Dominant, 3", "hypercholesterolemia, autosomal dominant, 3", "low density lipoprotein cholesterol level QTL 1", "hypercholesterolemia, autosomal dominant, type 3", "familial hypercholesterolemia caused by mutation in PCSK9", "LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 1", "low density lipoprotein cholesterol level quantitative trait locus 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypercholesterolemia, autosomal dominant, 3", "shortest_name_length": 3}
{"curie": "UMLS:C0917812", "names": ["Tetanilla", "Tetanillas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tetanilla", "shortest_name_length": 9}
{"curie": "MONDO:0016273", "names": ["germ cell cancer of corpus uteri", "germ cell cancer of the corpus uteri", "body of uterus malignant germ cell tumor", "malignant germ cell tumor of corpus uteri", "malignant germ cell tumor of the corpus uteri"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant germ cell tumor of corpus uteri", "shortest_name_length": 32}
{"curie": "MONDO:0021177", "names": ["Autoimmune hepatitis type 3", "autoimmune hepatitis type 3", "Autoimmune hepatitis type 3 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune hepatitis type 3", "shortest_name_length": 27}
{"curie": "UMLS:C2936718", "names": ["Fetal Cerebral Ventriculomegaly", "Cerebral Ventriculomegaly, Fetal", "Ventriculomegaly, Fetal Cerebral", "Fetal Cerebral Ventriculomegalies", "Ventriculomegalies, Fetal Cerebral", "Cerebral Ventriculomegalies, Fetal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fetal Cerebral Ventriculomegaly", "shortest_name_length": 31}
{"curie": "UMLS:C4764345", "names": ["Metastatic Sarcomatoid Urothelial Carcinoma", "Metastatic Sarcomatoid Bladder Urothelial Carcinoma", "Metastatic Sarcomatoid Urothelial Carcinoma of the Bladder", "Metastatic Infiltrating Bladder Urothelial Carcinoma, Sarcomatoid Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Infiltrating Bladder Urothelial Carcinoma, Sarcomatoid Variant", "shortest_name_length": 43}
{"curie": "MONDO:0000078", "names": ["ACPS", "acrocephalopolysyndactyly", "Acrocephalopolysyndactyly", "Acroencephalopolysyndactyly syndrome", "Acrocephalopolysyndactyly (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acrocephalopolysyndactyly", "shortest_name_length": 4}
{"curie": "MONDO:0012927", "names": ["HPE10", "Del(1)(q41q42)", "monosomy 1q41q42", "Monosomy 1q41q42", "monosomy 1q41-q42", "deletion 1q41-q42", "HOLOPROSENCEPHALY 10", "holoprosencephaly 10", "Holoprosencephaly 10", "1q41-q42 deletion syndrome", "1q41q42 microdeletion syndrome", "1q41-q42 microdeletion syndrome", "CHROMOSOME 1q41-q42 DELETION SYNDROME", "chromosome 1q41-q42 deletion syndrome", "1q41q42 microdeletion syndrome (disorder)", "chromosome 1q41-q42 deletion syndrome, isolated cases", "Holoprosencephaly with Microphthalmia and First Branchial Arch Anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 1q41-q42 deletion syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0004433", "names": ["penis papillary carcinoma", "Papillary Penile Carcinoma", "papillary penile carcinoma", "papillary carcinoma of penis", "Papillary Carcinoma of Penis", "Papillary Carcinoma of the Penis", "papillary carcinoma of the penis", "papillary penile squamous carcinoma", "Papillary Penile Squamous Carcinoma", "Papillary Squamous Carcinoma of Penis", "papillary squamous carcinoma of penis", "papillary carcinoma of penis (diagnosis)", "papillary squamous carcinoma of the penis", "Papillary Squamous Carcinoma of the Penis", "squamous carcinoma of penis, Papillary type", "Squamous Carcinoma of Penis, Papillary Type", "squamous carcinoma of penis, papillary type", "Squamous Carcinoma of the Penis, Papillary Type", "squamous carcinoma of the penis, papillary type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papillary carcinoma of the penis", "shortest_name_length": 25}
{"curie": "MONDO:0009624", "names": ["MCCRP1", "Pseudotoxoplasmosis syndrome", "microcephaly and chorioretinopathy 1", "microcephaly and chorioretinopathy type 1", "TUBGCP6 microcephaly and chorioretinopathy", "MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 1", "microcephaly and chorioretinopathy, autosomal recessive, 1", "autosomal recessive chorioretinopathy-microcephaly syndrome", "microcephaly and chorioretinopathy, autosomal recessive, type 1", "Microcephaly and Chorioretinopathy, Autosomal Recessive, Type 1", "microcephaly and chorioretinopathy caused by mutation in TUBGCP6", "autosomal recessive chorioretinopathy-microcephaly-intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly and chorioretinopathy 1", "shortest_name_length": 6}
{"curie": "MONDO:0013901", "names": ["SPGF10", "SEPT12 azoospermia", "spermatogenic failure 10", "SPERMATOGENIC FAILURE 10", "spermatogenic failure type 10", "azoospermia caused by mutation in SEPT12", "spermatogenic failure with defective sperm annulus", "SPERMATOGENIC FAILURE WITH DEFECTIVE SPERM ANNULUS", "Spermatogenic failure with defective sperm annulus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 10", "shortest_name_length": 6}
{"curie": "MONDO:0022858", "names": ["continuous spike-wave during slow sleep syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "continuous spike-wave during slow sleep syndrome", "shortest_name_length": 48}
{"curie": "UMLS:C0339170", "names": ["Conjunctivitis fungal", "Fungal conjunctivitis", "Fungal conjunctivitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fungal conjunctivitis", "shortest_name_length": 21}
{"curie": "UMLS:C1644176", "names": ["Neoplasm of lacrimal duct", "Lacrimal Drainage System Neoplasm", "Neoplasm of lacrimal drainage system", "eye neoplasm lacrimal drainage system", "Neoplasm of lacrimal drainage system (disorder)", "Neoplasm of lacrimal drainage system (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplasm of lacrimal drainage system", "shortest_name_length": 25}
{"curie": "MONDO:0014112", "names": ["CFC2", "cardiofaciocutaneous syndrome 2", "CARDIOFACIOCUTANEOUS SYNDROME 2", "kras cardiofaciocutaneous syndrome", "KRAS cardiofaciocutaneous syndrome", "cardiofaciocutaneous syndrome type 2", "cardiofaciocutaneous syndrome caused by mutation in KRAS", "cardiofaciocutaneous syndrome caused by mutation in kras"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiofaciocutaneous syndrome 2", "shortest_name_length": 4}
{"curie": "MONDO:0009205", "names": ["EASTMAN-BIXLER SYNDROME", "Eastman-Bixler syndrome", "Eastman Bixler syndrome", "faciocardiorenal syndrome", "Faciocardiorenal syndrome", "FACIOCARDIORENAL SYNDROME", "Faciocardiorenal syndrome (disorder)", "faciocardiorenal syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "faciocardiorenal syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0043339", "names": ["Lathyrism", "LATHYRISM", "lathyrism", "Neurolathyrism", "NEUROLATHYRISM", "neurolathyrism", "vetchling poisoning", "Vetchling poisoning", "Lathyrus species poisoning", "Lathyrus species poisoning (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lathyrism", "shortest_name_length": 9}
{"curie": "OMIM:609338", "names": ["CIMT1", "CAROTID INTIMAL MEDIAL THICKNESS 1", "Carotid Intimal Medial Thickness 1", "INTIMAL MEDIAL THICKNESS OF INTERNAL CAROTID ARTERY", "Intimal Medial Thickness of Internal Carotid Artery"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 5}
{"curie": "MONDO:0030073", "names": ["MITCH", "MITCHELL SYNDROME", "Mitchell syndrome", "ACOX1 dysregulation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mitchell syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0014624", "names": ["BRWNS", "Brown", "Brown anomaly", "BROWN SYNDROME", "brown syndrome", "Brown syndrome", "browns syndrome", "brown's syndrome", "Brown's syndrome", "Brown's sheath syndrome", "brown's sheath syndrome", "Brown Tendon Sheath Syndrome", "Brown tendon sheath syndrome", "Brown's tendon sheath syndrome", "Brown's Tendon Sheath Syndrome", "Syndrome, Brown's Tendon Sheath", "Tendon Sheath Syndrome of Brown", "Brown's (tendon) sheath syndrome", "Superior oblique tendon sheath syndrome", "superior oblique tendon sheath syndrome", "tendon sheath adherence, Superior oblique", "Brown's tendon sheath syndrome (disorder)", "Brown's tendon sheath syndrome (diagnosis)", "SOTSS - Superior oblique tendon sheath syndrome", "SOTSS - superior oblique tendon sheath syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brown syndrome", "shortest_name_length": 5}
{"curie": "DOID:0080685", "names": ["aortic dissection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic dissection", "shortest_name_length": 17}
{"curie": "UMLS:C1535897", "names": ["Hair Tourniquet", "Hair-thread tourniquet syndrome", "Hair-Thread Tourniquet Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hair-thread tourniquet syndrome", "shortest_name_length": 15}
{"curie": "UMLS:C1565662", "names": ["Acute renal impairment", "Acute Renal Insufficiency", "RENAL INSUFFICIENCY ACUTE", "acute renal insufficiency", "Acute renal insufficiency", "Renal Insufficiency, Acute", "Renal insufficiency, Acute", "Acute Kidney Insufficiency", "insufficiency; renal, acute", "Kidney Insufficiency, Acute", "Renal insufficiency (acute)", "Acute Renal Insufficiencies", "Acute Kidney Insufficiencies", "Renal Insufficiencies, Acute", "Kidney Insufficiencies, Acute", "Acute renal impairment (disorder)", "Acute renal insufficiency (disorder)", "acute renal insufficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Kidney Insufficiency", "shortest_name_length": 22}
{"curie": "MONDO:0013460", "names": ["OI12", "OI, type 12", "OI, TYPE XII", "SP7 osteogenesis imperfecta", "osteogenesis imperfecta type 12", "osteogenesis imperfecta type XII", "osteogenesis imperfecta, type 12", "osteogenesis imperfecta, type XII", "OSTEOGENESIS IMPERFECTA, TYPE XII", "osteogenesis imperfecta caused by mutation in SP7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteogenesis imperfecta type 12", "shortest_name_length": 4}
{"curie": "MONDO:0007519", "names": ["typus ediburgensis", "Typus Edinburgensis", "typus Edinburgensis", "Edinburgh malformation syndrome", "EDINBURGH MALFORMATION SYNDROME", "Edinburgh Malformation Syndrome", "Edinburgh malformation syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Edinburgh malformation syndrome", "shortest_name_length": 18}
{"curie": "UMLS:C1843323", "names": ["Van Buchem disease type 2", "Van Buchem Disease, Type 2", "Osteosclerosis of the skull and enlarged mandible"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Van Buchem disease type 2", "shortest_name_length": 25}
{"curie": "UMLS:C1336439", "names": ["Skin Cancer Stage IV", "Stage IV Skin Cancer", "Skin Carcinoma Stage IV", "Stage IV Skin Carcinoma", "Carcinoma of Skin Stage IV", "Stage IV Skin Cancer AJCC v7", "Carcinoma of the Skin Stage IV", "stage IV nonmelanoma skin cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Skin Cancer", "shortest_name_length": 20}
{"curie": "MONDO:0017529", "names": ["polysyndactyly, unilateral", "preaxial polydactyly type 4, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polysyndactyly, unilateral", "shortest_name_length": 26}
{"curie": "MONDO:0054761", "names": ["MCPH20", "microcephaly 20, primary, autosomal recessive", "MICROCEPHALY 20, PRIMARY, AUTOSOMAL RECESSIVE", "microcephaly 20, PRIMARY, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly 20, primary, autosomal recessive", "shortest_name_length": 6}
{"curie": "MONDO:0009595", "names": ["CHH", "Cartilage Hair Syndrome", "Cartilage hair syndrome", "cartilage hair hypoplasia", "cartilage-hair hypoplasia", "Cartilage Hair Hypoplasia", "CARTILAGE-HAIR HYPOPLASIA", "Cartilage-hair hypoplasia", "Cartilage-hair hypoplasia syndrome", "cartilage hair hypoplasia like syndrome", "metaphyseal chondrodysplasia McKusick type", "McKusick type metaphyseal chondrodysplasia", "Metaphyseal chondrodysplasia, McKusick type", "metaphyseal chondrodysplasia, McKusick type", "metaphyseal chondrodysplasia, Mckusick type", "METAPHYSEAL CHONDRODYSPLASIA, MCKUSICK TYPE", "Metaphyseal Chondrodysplasia, Recessive Type", "McKusick Metaphyseal Chondrodysplasia Syndrome", "autosomal recessive metaphyseal chondrodysplasia", "McKusick's metaphyseal chondrodysplasia syndrome", "Autosomal recessive metaphyseal chondrodysplasia", "Metaphyseal chondrodysplasia, McKusick type (disorder)", "Metaphyseal chondrodysplasia, McKusick type (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cartilage-hair hypoplasia", "shortest_name_length": 3}
{"curie": "UMLS:C0274435", "names": ["transfusion reaction", "TRANSFUSION REACTION", "Transfusion Reaction", "Transfusion reaction", "reactions transfusion", "transfusion reactions", "Transfusion Reactions", "Transfusion reaction NOS", "Transfusion reaction, NOS", "Adverse effect;transfusion", "Blood transfusion reaction", "blood reaction transfusion", "blood transfusion reaction", "Blood Transfusion Reaction", "blood reactions transfusion", "BLOOD TRANSFUSION REACTIONS", "blood transfusion reactions", "blood transfusion complication", "blood complication transfusion", "blood complications transfusion", "blood transfusion complications", "Blood transfusion reaction, NOS", "Unspecified transfusion reaction", "blood complications transfusions", "Complication of blood transfusion", "complication of blood transfusion", "Transfusion reaction, unspecified", "complications; transfusion, reaction", "transfusion; complications, reaction", "Blood transfusion reaction (disorder)", "Complication of blood transfusion, NOS", "blood transfusion reaction (diagnosis)", "blood transfusion complications (diagnosis)", "Blood Transfusion Associated Adverse Reactions", "Blood Transfusion-Associated Adverse Reactions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transfusion Reaction", "shortest_name_length": 20}
{"curie": "MONDO:0001705", "names": ["PRCA", "Red cell aplasia", "red cell aplasia", "Red Cell Aplasia", "red cell; aplasia", "aplasia; red cell", "red cell hypoplasia", "Red cell hypoplasia", "Erythrocyte Aplasia", "Pure red cell anemia", "Aplasia, Erythrocyte", "Erythrocyte Aplasias", "Red cell aplasia NOS", "pure red cell anemia", "Aplasia pure red cell", "anemia; pure red cell", "pure red cell aplasia", "pure red cell; anemia", "Pure red cell anaemia", "Pure Red-Cell Aplasia", "APLASIA PURE RED CELL", "Pure red cell aplasia", "Aplasia Pure Red Cell", "pure red-cell aplasia", "Pure Red Cell Aplasia", "Aplasias, Erythrocyte", "APLASIA, PURE RED CELL", "pure red cell; aplasia", "Pure Red-Cell Aplasias", "Red-Cell Aplasia, Pure", "aplasia cells pure red", "Red Cell Aplasia, Pure", "Aplasia, pure red cell", "Aplasia, Pure Red-Cell", "Red-Cell Aplasias, Pure", "Primary red cell aplasia", "primary red cell aplasia", "Pure red cell anemia, NOS", "Pure red cell aplasia, NOS", "aplasia; red cell, primary", "red cell; aplasia, primary", "Pure red cell anaemia, NOS", "Pure red cell aplasia (disorder)", "Primary acquired red cell aplasia", "Primary autoimmune red cell aplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pure red-cell aplasia", "shortest_name_length": 4}
{"curie": "UMLS:C5420341", "names": ["Salivary Gland Lymphoma", "Primary Salivary Gland Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Salivary Gland Lymphoma", "shortest_name_length": 23}
{"curie": "UMLS:C5669817", "names": ["Myeloid Neoplasms with Germline SAMD9L Mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myeloid Neoplasms with Germline SAMD9L Mutation", "shortest_name_length": 47}
{"curie": "UMLS:C0280370", "names": ["Stage II SCC of Oropharynx", "Stage II Oropharyngeal SCC", "Stage II SCC of the Oropharynx", "Stage II Oropharyngeal Epidermoid Carcinoma", "Stage II Epidermoid Carcinoma of Oropharynx", "oropharynx squamous cell carcinoma, stage II", "Stage II Squamous Cell Carcinoma of Oropharynx", "Oropharyngeal squamous cell carcinoma stage II", "Stage II Oropharyngeal Squamous Cell Carcinoma", "Stage II Epidermoid Carcinoma of the Oropharynx", "oropharyngeal squamous cell carcinoma, stage II", "epidermoid carcinoma of the oropharynx, stage II", "stage II squamous cell carcinoma of the oropharynx", "Stage II Squamous Cell Carcinoma of the Oropharynx", "Stage II Oropharyngeal Throat Squamous Cell Cancer", "squamous cell carcinoma of the oropharynx, stage II", "Stage II Oropharyngeal Squamous Cell Carcinoma AJCC v6", "Stage II Oropharyngeal Squamous Cell Carcinoma AJCC v7", "Stage II Oropharyngeal Squamous Cell Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oropharyngeal squamous cell carcinoma stage II", "shortest_name_length": 26}
{"curie": "MONDO:0019446", "names": ["papular mucinosis", "localized lichen myxedematosus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "localized lichen myxedematosus", "shortest_name_length": 17}
{"curie": "MONDO:0012315", "names": ["deletion 10q", "10q monosomy", "monosomy 10q", "10q deletion", "Monosomy 10qter", "monosomy 10qter", "Distal monosomy 10q", "Distal deletion 10q", "distal monosomy 10q", "distal deletion 10q", "partial monosomy 10q", "Telomeric deletion 10q", "telomeric deletion 10q", "chromosome 10q deletion", "distal monosomy type 10q", "distal 10q deletion syndrome", "Distal monosomy 10q syndrome", "chromosome 10q26 deletion syndrome", "CHROMOSOME 10q26 DELETION SYNDROME", "Chromosome 10q26 Deletion Syndrome", "Distal monosomy 10q syndrome (disorder)", "terminal chromosome 10Q26 deletion syndrome", "Terminal Chromosome 10q26 Deletion Syndrome", "terminal chromosome 10q26 deletion syndrome", "TERMINAL CHROMOSOME 10q26 DELETION SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal 10q deletion syndrome", "shortest_name_length": 12}
{"curie": "UMLS:C4540536", "names": ["PITUITARY TUMOR 3, GROWTH HORMONE-SECRETING, SOMATIC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PITUITARY TUMOR 3, GROWTH HORMONE-SECRETING, SOMATIC", "shortest_name_length": 52}
{"curie": "UMLS:C0340909", "names": ["AV FISTULA THROMBOSIS", "AV fistula thrombosis", "AV Fistula Thrombosis", "Arteriovenous fistula clotted", "arteriovenous fistula thrombosis", "Arteriovenous fistula thrombosis", "Arteriovenous Fistula Thrombosis", "Thrombosis arteriovenous fistula", "THROMBOSIS ARTERIO-VENOUS FISTULA", "Arteriovenous fistula thrombosis (disorder)", "arteriovenous fistula thrombosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arteriovenous fistula thrombosis", "shortest_name_length": 21}
{"curie": "UMLS:C1336135", "names": ["Stage IB Hodgkin Lymphoma", "Hodgkin's Disease Stage IB", "Stage IB Hodgkin's Disease", "Stage IB Hodgkin's Lymphoma", "Hodgkin's Lymphoma Stage IB", "Ann Arbor Stage IB Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage IB Hodgkin Lymphoma", "shortest_name_length": 25}
{"curie": "MONDO:0010878", "names": ["SPG6", "Fsp3", "Spg6", "FSP3", "spastic paraplegia 6", "hereditary spastic paraplegia 6", "NIPA1 hereditary spastic paraplegia", "hereditary spastic paraplegia type 6", "autosomal dominant spastic paraplegia 6", "spastic paraplegia 6, autosomal dominant", "Spastic paraplegia 6, autosomal dominant", "SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT", "autosomal dominant spastic paraplegia type 6", "Autosomal dominant spastic paraplegia type 6", "familial spastic paraplegia autosomal dominant 3", "Familial spastic paraplegia, autosomal dominant 3", "Familial Spastic Paraplegia, Autosomal Dominant, 3", "familial spastic paraplegia, autosomal dominant, 3", "FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 3", "SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT (disorder)", "Autosomal dominant familial spastic paraplegia type 3", "autosomal dominant familial spastic paraplegia type 3", "familial spastic paraplegia autosomal dominant type 6", "Autosomal dominant spastic paraplegia type 6 (disorder)", "Autosomal dominant spastic paraplegia type 6 (diagnosis)", "hereditary spastic paraplegia caused by mutation in NIPA1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 6", "shortest_name_length": 4}
{"curie": "UMLS:C5670683", "names": ["Stage IVA Cervical Cancer FIGO 2009", "Stage IVA Cervical Carcinoma FIGO 2009"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Cervical Cancer FIGO 2009", "shortest_name_length": 35}
{"curie": "UMLS:C5239283", "names": ["Locally Advanced Esophageal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Esophageal Carcinoma", "shortest_name_length": 37}
{"curie": "UMLS:C0854846", "names": ["Stage II Intestinal T-Cell Lymphoma", "Intestinal T-cell lymphoma stage II", "Intestinal T-Cell Lymphoma Stage II", "Stage II Enteropathy-type T-Cell Lymphoma", "Stage II Enteropathy-Associated T-Cell Lymphoma", "Ann Arbor Stage II Enteropathy-Associated T-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal T-cell lymphoma stage II", "shortest_name_length": 35}
{"curie": "MONDO:0009223", "names": ["HH23", "Fertile eunuch", "Pasqualini syndrome", "PASQUALINI SYNDROME", "FERTILE EUNUCH SYNDROME", "fertile eunuch syndrome", "Fertile eunuch syndrome", "syndrome; fertile eunuch", "fertile eunuch; syndrome", "Isolated lutropin deficiency", "46,XY DSD due to LHB deficiency", "LHB hypogonadotropic hypogonadism", "Isolated lutropin deficiency (disorder)", "Leydig cell hypoplasia due to LHB deficiency", "leydig cell hypoplasia due to LHB deficiency", "hypogonadotropic hypogonadism 23 without anosmia", "HYPOGONADOTROPIC HYPOGONADISM 23 WITHOUT ANOSMIA", "hypogonadotropic hypogonadism caused by mutation in LHB", "46,XY disorder of sex development due to LHB deficiency", "hypogonadotropic hypogonadism 23 with or without anosmia", "HYPOGONADOTROPIC HYPOGONADISM 23 WITH OR WITHOUT ANOSMIA", "46,XY DSD due to luteinizing hormone subunit beta deficiency", "Leydig cell hypoplasia due to luteinizing hormone subunit beta deficiency", "46,XY disorder of sex development due to luteinizing hormone subunit beta deficiency", "eunuchoidism with spermatogenesis, normal FSH and low or normal interstitial cell-stimulating hormone (ICSH)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadotropic hypogonadism 23 with or without anosmia", "shortest_name_length": 4}
{"curie": "MONDO:0006406", "names": ["Sarcomatoid carcinoma", "sarcomatoid carcinoma", "Sarcomatoid Carcinoma", "spindle cell carcinoma", "Spindle cell carcinoma", "spindle-cell carcinoma", "Spindle-Cell Carcinoma", "Spindle Cell Carcinoma", "Spindle-Cell Carcinomas", "Carcinoma, Spindle-Cell", "Carcinoma, Spindle Cell", "Pseudosarcomatous carcinoma", "Pseudosarcomatous Carcinoma", "Spindle cell carcinoma, NOS", "pseudosarcomatous carcinoma", "Polypoid squamous cell carcinoma", "carcinoma, spindle cell, malignant", "CARCINOMA, SPINDLE CELL, MALIGNANT", "spindle cell carcinoma (diagnosis)", "pseudosarcomatous carcinoma (diagnosis)", "spindle cell carcinoma (morphologic abnormality)", "Spindle cell carcinoma (morphologic abnormality)", "Pseudosarcomatous carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sarcomatoid carcinoma", "shortest_name_length": 21}
{"curie": "MONDO:0005776", "names": ["Gnathomiasis", "gnathomiasis", "gnathostomosis", "Gnathostomosis", "Gnathostomiases", "Gnathostomiasis", "gnathostomiasis", "GNATHOSTOMIASIS", "Gnathostoma infection", "Gnathostoma Infection", "Infection, Gnathostoma", "Gnathostoma Infections", "Infections, Gnathostoma", "Infection by Gnathostoma", "gnathostomiasis (diagnosis)", "Infection by Gnathostoma, NOS", "Infection caused by Gnathostoma", "Infectious Disease by Gnathostoma", "infectious disease by Gnathostoma", "Infection caused by Gnathostoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gnathomiasis", "shortest_name_length": 12}
{"curie": "MONDO:0005362", "names": ["ED", "impotent", "Impotent", "impotence", "Impotence", "IMPOTENCE", "Impotence NOS", "Impotence nos", "male impotence", "Male Impotence", "Impotence, NOS", "impotence, male", "Impotence, Male", "sexual impotence", "Sexual impotence", "Erection failure", "Erectile disorder", "erection; failure", "Abnormal erection", "failure; erection", "disorder; erectile", "erectile; disorder", "Failure of erection", "erectile dysfunction", "Erectile disturbance", "dysfunction erection", "dysfunction erectile", "Erectile dysfunction", "Erectile Dysfunction", "erection dysfunction", "ERECTILE DYSFUNCTION", "Dysfunction;erection", "erectile dysfunctions", "disturbance; erectile", "Dysfunction, Erectile", "male sexual impotence", "dysfunction, erectile", "Male Sexual Impotence", "Sexual impotence, NOS", "male erectile disorder", "Impotence, Male Sexual", "male erectile Disorder", "Erectile abnormalities", "sexual impotence, Male", "impotence, male sexual", "Sexual Impotence, Male", "Male erectile disorder", "Male Erectile Disorder", "dysfunctioning erectile", "Erectile dysfunction NOS", "male erectile dysfunction", "Male erectile dysfunction", "sexual impotence (finding)", "PENILE ERECTION IMPAIRMENT", "Dysfunction;sexual;impotence", "erectile dysfunction (disease)", "Difficulty getting an erection", "Erectile dysfunction (disorder)", "male erectile disorder (diagnosis)", "Difficulty getting a full erection", "male erectile dysfunction (diagnosis)", "Male erectile dysfunction, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erectile dysfunction", "shortest_name_length": 2}
{"curie": "MONDO:0035124", "names": ["linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies", "shortest_name_length": 89}
{"curie": "MONDO:0012243", "names": ["BILU", "BILU syndrome", "BILU Syndrome", "Bilu syndrome", "BILU SYNDROME", "HOFFMAN SYNDROME", "Hoffman syndrome", "BILU (B-cell immunodeficiency, limb, urogenital) syndrome", "B-cell immunodeficiency-limb anomaly-urogenital malformation syndrome", "B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome", "B-Cell Immunodeficiency, Distal Limb Anomalies, And Urogenital Malformations", "B-cell immunodeficiency, distal limb anomalies, and urogenital malformations", "B-CELL IMMUNODEFICIENCY, DISTAL LIMB ANOMALIES, AND UROGENITAL MALFORMATIONS", "B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-cell immunodeficiency, distal limb anomalies, and urogenital malformations", "shortest_name_length": 4}
{"curie": "MONDO:0700071", "names": ["POMT2 myopathy", "POMT2-related myopathy", "myopathy caused by mutation in POMT2", "myopathy caused by variation in POMT2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy caused by variation in POMT2", "shortest_name_length": 14}
{"curie": "UMLS:C5206375", "names": ["Refractory Colon Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Colon Adenocarcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0002876", "names": ["Cervical adenosarcoma", "cervical adenosarcoma", "Cervical Adenosarcoma", "uterine cervix adenosarcoma", "Adenosarcoma of cervix uteri", "adenosarcoma of uterine cervix", "cervical Mullerian adenosarcoma", "cervical Müllerian adenosarcoma", "Cervical Müllerian Adenosarcoma", "Cervical Mullerian Adenosarcoma", "adenosarcoma of the cervix uteri", "Adenosarcoma of the cervix uteri", "cervical Muellerian adenosarcoma", "Adenosarcoma of cervix uteri (disorder)", "Adenosarcoma of cervix uteri (diagnosis)", "cervical malignant neoplasm adenosarcoma of cervix uteri"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical adenosarcoma", "shortest_name_length": 21}
{"curie": "UMLS:C0268561", "names": ["P-protein deficiency", "P protein deficiency", "Glycine decarboxylase deficiency", "Type I Nonketotic Hyperglycinemia", "Nonketotic Hyperglycinemia, Type I", "Nonketotic hyperglycinemia, type I", "Non-ketotic hyperglycinemia type I", "Non-ketotic hyperglycinaemia type I", "Nonketotic hyperglycinaemia, type I", "Hyperglycinemia, Nonketotic, Type I", "Glycine dehydrogenase decarboxylating deficiency", "Non-ketotic hyperglycinemia P protein deficiency", "Non-ketotic hyperglycinaemia P protein deficiency", "Glycine dehydrogenase (decarboxylating) deficiency", "Glycine dehydrogenase (decarboxylating) deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyperglycinemia, Nonketotic, Type I", "shortest_name_length": 20}
{"curie": "MONDO:0025389", "names": ["Bang", "bang disease", "BANG DISEASE", "Bang Disease", "Disease, Bang", "Bangs disease", "disease, bang", "bangs disease", "Bangs Disease", "Bang's disease", "bang's disease", "Bang's Disease", "disease, bang's", "Disease, Bang's", "Brucella abortus", "brucella abortus", "bovine brucellosis", "Bovine brucellosis", "Bovine Brucellosis", "Bovine Brucelloses", "bovine Brucelloses", "Brucelloses, Bovine", "brucellosis, bovine", "Brucelloses, bovine", "Brucellosis, Bovine", "Contagious abortion", "abortus; brucellosis", "brucellosis; abortus", "Brucellosis in cattle", "Brucella abortus infection", "brucella abortus infection", "Brucella abortus brucellosis", "Brucella; infection, abortus", "infection; Brucella, abortus", "Infection due to Brucella abortus", "infection due to Brucella abortus", "Brucellosis due to Brucella abortus", "Infection caused by Brucella abortus", "infection due to Brucella abortus (diagnosis)", "Infection caused by Brucella abortus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brucellosis, bovine", "shortest_name_length": 4}
{"curie": "MONDO:0020770", "names": ["SCAN3", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE, WITH AXONAL NEUROPATHY 3", "spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3", "shortest_name_length": 5}
{"curie": "UMLS:C0027804", "names": ["Beard", "NEURASTHENIA", "Neurasthenia", "neurasthenia", "Neurasthaenia", "Beard's disease", "Nervous debility", "Fatigue neurosis", "Nervous Debility", "nervous debility", "fatigue neurosis", "debility; nervous", "neurosis; fatigue", "fatigue; neurosis", "asthenia; nervous", "nervous; debility", "nervous; asthenia", "neurosis; asthenic", "neurotic; asthenia", "asthenia; neurotic", "asthenic; neurosis", "Neurasthenic neurosis", "Neurasthenic Neurosis", "Neurasthenic Neuroses", "Neuroses, Neurasthenic", "Neurasthaenic neurosis", "Neurosis, neurasthenic", "Bodily distress disorder", "Somatic symptom disorder", "bodily distress disorder", "Bodily Distress Disorder", "psychoneurotic; asthenia", "asthenia; psychoneurotic", "neurasthenia (diagnosis)", "Bodily Distress Disorders", "Disorder, Bodily Distress", "Distress Disorder, Bodily", "Somatic symptom disorders", "asthenia; psychophysiologic", "psychophysiologic; asthenia", "Bodily distress disorder (disorder)", "bodily distress disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neurasthenia", "shortest_name_length": 5}
{"curie": "MONDO:0004462", "names": ["Extrahepatic Bile Duct MCN", "extrahepatic bile duct cystadenoma", "Extrahepatic Bile Duct Cystadenoma", "Cystadenoma of Extrahepatic Bile Duct", "cystadenoma of extrahepatic bile duct", "Cystadenoma of the extrahepatic bile duct", "cystadenoma of the extrahepatic bile duct", "Cystadenoma of the Extrahepatic Bile Duct", "Extrahepatic Bile Duct Mucinous Cystic Neoplasm", "extrahepatic bile duct mucinous cystic neoplasm", "cystadenoma of extrahepatic bile duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extrahepatic bile duct cystadenoma", "shortest_name_length": 26}
{"curie": "UMLS:C4724994", "names": ["Refractory Paranasal Sinus Squamous Cell Cancer", "Refractory Paranasal Sinus Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Paranasal Sinus Squamous Cell Carcinoma", "shortest_name_length": 47}
{"curie": "MONDO:0023513", "names": ["Jeune syndrome situs inversus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jeune syndrome situs inversus", "shortest_name_length": 29}
{"curie": "MONDO:0010849", "names": ["PPKB", "Bothnian type palmoplantar keratoderma", "PALMOPLANTAR KERATODERMA, BOTHNIAN TYPE", "Palmoplantar keratoderma, Bothnian type", "palmoplantar keratoderma, Bothnian type", "Diffuse palmoplantar keratoderma, Bothnian type", "diffuse palmoplantar keratoderma, Bothnian type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "palmoplantar keratoderma, Bothnian type", "shortest_name_length": 4}
{"curie": "MONDO:0002381", "names": ["sweat gland tumor", "Sweat gland tumor", "gland sweat tumor", "Sweat Gland Tumor", "Sweat gland tumour", "gland sweat tumors", "sweat gland tumour", "tumor of sweat gland", "sweat gland neoplasm", "Tumor of Sweat Gland", "Sweat Gland Neoplasm", "gland neoplasm sweat", "gland sweat neoplasms", "sweat gland neoplasms", "Neoplasm, Sweat Gland", "Sweat Gland Neoplasms", "Sweat gland tumor NOS", "Sweat gland tumour NOS", "Neoplasms, Sweat Gland", "Sweat gland tumor, NOS", "Neoplasm of Sweat Gland", "neoplasm of sweat gland", "Neoplasm of sweat gland", "Sweat gland tumour, NOS", "tumor of the sweat gland", "Tumor of the Sweat Gland", "tumor of the Sweat gland", "sweat gland benign neoplasm", "Neoplasm of the Sweat Gland", "neoplasm of the sweat gland", "sweat gland neoplasm (disease)", "Neoplasm of sweat gland (disorder)", "Neoplasm of sweat gland (diagnosis)", "Tumor of skin with eccrine differentiation", "sweat gland tumor (morphologic abnormality)", "Sweat gland tumor (morphologic abnormality)", "Tumour of skin with eccrine differentiation", "neoplasm of integumentary system sweat gland", "sweat gland tumor NOS (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sweat gland neoplasm", "shortest_name_length": 17}
{"curie": "MONDO:0012257", "names": ["Cerebrorenodigital syndrome", "CEREBRORENODIGITAL syndrome with limb malformations and triradiate acetabula", "CEREBRORENODIGITAL SYNDROME WITH LIMB MALFORMATIONS AND TRIRADIATE ACETABULA", "Cerebrorenodigital Syndrome with Limb Malformations and Triradiate Acetabula"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebrorenodigital syndrome", "shortest_name_length": 27}
{"curie": "UMLS:C5419194", "names": ["Unresectable Colorectal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Colorectal Adenocarcinoma", "shortest_name_length": 38}
{"curie": "UMLS:C5419874", "names": ["Pancreatic IMPC", "Pancreatic Invasive Micropapillary Carcinoma", "Pancreatic Invasive Micropapillary Adenocarcinoma", "Invasive Pancreatic Micropapillary Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Invasive Pancreatic Micropapillary Adenocarcinoma", "shortest_name_length": 15}
{"curie": "UMLS:C5205580", "names": ["Prostate Acinar Adenocarcinoma, Pleomorphic Giant Cell Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Acinar Adenocarcinoma, Pleomorphic Giant Cell Variant", "shortest_name_length": 62}
{"curie": "MONDO:0100305", "names": ["BAAT deficiency", "bile acid CoA:amino acid N-acyltransferase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bile acid CoA:amino acid N-acyltransferase deficiency", "shortest_name_length": 15}
{"curie": "UMLS:C1696083", "names": ["Oral Cavity Fistula", "Oral cavity fistula"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral Cavity Fistula", "shortest_name_length": 19}
{"curie": "MONDO:0010176", "names": ["OFD6", "Ofds 6", "OFDS VI", "Varadi syndrome", "Varadi Syndrome", "Váradi syndrome", "VARADI SYNDROME", "Varadi Papp syndrome", "Varadi-Papp Syndrome", "Varadi-Papp syndrome", "Váradi-Papp syndrome", "VARADI-PAPP SYNDROME", "Juberg-Hayward syndrome", "Orofaciodigital syndrome 6", "orofaciodigital syndrome 6", "digito-oro-palatal syndrome", "OROFACIODIGITAL SYNDROME VI", "orofaciodigital syndrome VI", "Orofaciodigital Syndrome VI", "digito-orofacial syndrome VI", "palatal-digital-oral syndrome", "orofaciodigital syndrome type 6", "Orofaciodigital Syndrome Type 6", "oral-facial-digital syndrome VI", "Orofaciodigital syndrome type 6", "Juberg syndrome with polydactyly", "orofaciodigital (OFD) syndrome VI", "oral-facial-digital syndrome type 6", "Oral-facial-digital syndrome type 6", "oral-Facial-digital syndrome, type 6", "Oral-facial-digital syndrome, type 6", "Oral-Facial-Digital Syndrome, Type VI", "ORAL-FACIAL-DIGITAL SYNDROME, TYPE VI", "Joubert syndrome with orofaciodigital defect", "Joubert syndrome with oro-facial-digital syndrome", "Joubert syndrome with oral-facial-digital syndrome", "Polydactyly cleft lip palate psychomotor retardation", "polydactyly cleft lip palate psychomotor retardation", "Joubert syndrome with orofaciodigital defect (disorder)", "polydactyly - cleft lip/palate - psychomotor retardation", "polydactyly-cleft lip/palate-psychomotor retardation syndrome", "Polydactyly-cleft lip/palate-psychomotor retardation syndrome", "polydactyly, cleft Lip/palate or lingual lump, and psychomotor retardation", "POLYDACTYLY, CLEFT LIP/PALATE OR LINGUAL LUMP, AND PSYCHOMOTOR RETARDATION", "Polydactyly, Cleft Lip-Palate or Lingual Lump, and Psychomotor Retardation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orofaciodigital syndrome type 6", "shortest_name_length": 4}
{"curie": "UMLS:C5446575", "names": ["Conjunctival Angiosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conjunctival Angiosarcoma", "shortest_name_length": 25}
{"curie": "UMLS:C2077203", "names": ["Recurrent Laryngeal Nerve Trauma", "Recurrent Laryngeal Nerve Injury", "Recurrent Laryngeal Nerve Injuries", "injury of recurrent laryngeal nerve", "Recurrent Laryngeal Neuropathy, Traumatic", "injury of recurrent laryngeal nerve (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Laryngeal Nerve Injuries", "shortest_name_length": 32}
{"curie": "MONDO:0019518", "names": ["WS4", "Waardenburg-Shah syndrome", "Waardenburg-Shah Syndrome", "Shah-Waardenburg syndrome", "Waardenburg Syndrome Type 4", "Waardenburg syndrome type 4", "Waardenburg Syndrome Type IV", "Waardenburg syndrome type IV", "Waardenburg-Hirschsprung disease", "Waardenburg-Hirschsprung syndrome", "Hirschsprung disease with pigmentary anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Waardenburg-Shah syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0001441", "names": ["pica", "PICA", "Pica", "pica; in", "pica disease", "Pica Disease", "pica disorder", "Pica (disorder)", "pica (diagnosis)", "Abnormal craving", "Pica Eating Disorder", "Pica eating disorder", "pica eating disorder", "Eats abnormal objects", "craving unusual or nonfood items", "craving unusual or nonfood items (pica)", "craving unusual or nonfood items (pica) (symptom)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pica disease", "shortest_name_length": 4}
{"curie": "MONDO:0018359", "names": ["neonatal DM", "neonatal dermatomyositis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal dermatomyositis", "shortest_name_length": 11}
{"curie": "MONDO:0002184", "names": ["drug-induced hepatitis", "drug-induced chronic hepatitis", "Drug-induced chronic hepatitis", "chronic drug-induced hepatitis", "Hepatitis, Chronic, Drug-Induced", "Hepatitis, Chronic, Drug-Related", "Drug-induced chronic hepatitis (disorder)", "chronic drug-induced hepatitis (diagnosis)", "Chemical and Drug Induced Liver Injury, Chronic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "drug-induced hepatitis", "shortest_name_length": 22}
{"curie": "UMLS:C0280625", "names": ["Stage II Uterine Sarcoma", "stage II uterine sarcoma", "uterine sarcoma, stage II", "Stage II Uterine Sarcoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Uterine Sarcoma AJCC v7", "shortest_name_length": 24}
{"curie": "MONDO:0020501", "names": ["CCHF", "congo fever", "Congo fever", "CHF Congo virus", "Congo virus; fever", "fever; Congo virus", "Congo Virus Infection", "Infection, Congo Virus", "Congo hemorrhagic fever", "Crimean hemorrhagic fever", "crimean hemorrhagic fever", "Crimean Hemorrhagic Fever", "Hemorrhagic Fever, Crimean", "Crimean haemorrhagic fever", "Fever, Crimean Hemorrhagic", "Congo-Crimean hemorrhagic fever", "Central Asian hemorrhagic fever", "Crimean Congo Hemorrhagic Fever", "crimean congo hemorrhagic fever", "Crimean-Congo hemorrhagic fever", "Congo Crimean hemorrhagic fever", "CHF - Crimean hemorrhagic fever", "Congo-Crimean Hemorrhagic Fever", "crimean-congo hemorrhagic fever", "Crimean-Congo Hemorrhagic Fever", "Congo Crimean Hemorrhagic Fever", "Fever, Crimean-Congo Hemorrhagic", "fever; Crimean-Congo hemorrhagic", "crimean congo haemorrhagic fever", "hemorrhagic fever; Crimean-Congo", "crimean-congo haemorrhagic fever", "Central Asian; hemorrhagic fever", "Crimean-Congo; hemorrhagic fever", "CHF - Crimean haemorrhagic fever", "Hemorrhagic Fever, Congo-Crimean", "Fever, Congo-Crimean Hemorrhagic", "Crimean Congo Haemorrhagic Fever", "Crimean-Congo hemorrhagic; fever", "Crimean-Congo haemorrhagic fever", "Central Asian haemorrhagic fever", "Hemorrhagic Fever, Crimean-Congo", "hemorrhagic fever; Central Asian", "Congo-Crimean haemorrhagic fever", "HEMORRHAGIC FEVER, CRIMEAN-CONGO", "Crimean-Congo Haemorrhagic Fever", "Fever, Crimean-Congo Haemorrhagic", "Haemorrhagic Fever, Crimean-Congo", "CCHF - Crimean-Congo hemorrhagic fever", "Viral hemorrhagic fever, Crimean-Congo", "Asian; Central Asian hemorrhagic fever", "CCHF - Crimean-Congo haemorrhagic fever", "Viral haemorrhagic fever, Crimean-Congo", "Congo-Crimean hemorrhagic fever (disorder)", "Congo Crimean hemorrhagic fever (diagnosis)", "Crimean hemorrhagic fever [CHF Congo virus]", "Congo-Crimean hemorrhagic fever viral infection", "Congo-Crimean haemorrhagic fever viral infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Crimean-Congo hemorrhagic fever", "shortest_name_length": 4}
{"curie": "MONDO:0006714", "names": ["coronary aneurysm", "Coronary Aneurysm", "aneurysm; coronary", "Coronary Aneurysms", "Aneurysm, Coronary", "coronary; aneurysm", "coronary aneurysms", "Aneurysms, Coronary", "Coronary artery ectasia", "aneurysm coronary artery", "CORONARY ARTERY ANEURYSM", "aneurysm artery coronary", "coronary artery aneurysm", "Coronary Artery Aneurysm", "Coronary artery aneurysm", "Aneurysm;artery;coronary", "Coronary artery aneurysms", "coronary artery aneurysms", "Coronary artery dilatation", "aneurysm arteries coronary", "aneurysm of coronary artery", "aneurysm of coronary vessels", "Aneurysm of coronary vessels", "Coronary arterial dilatation", "aneurysmal lesion of coronary artery", "Aneurysmal lesion of coronary artery", "aneurysm of coronary artery (diagnosis)", "Aneurysm of coronary vessels (disorder)", "arteriovenous aneurysm of coronary vessels", "Arteriovenous aneurysm of coronary vessels"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coronary aneurysm", "shortest_name_length": 17}
{"curie": "MONDO:0004544", "names": ["CHOM", "chordoid meningioma", "Chordoid Meningioma", "Chordoid meningioma", "Meningioma, chordoid", "meningioma, chordoid", "meningioma, chordoid (morphologic abnormality)", "Meningioma, chordoid (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chordoid meningioma", "shortest_name_length": 4}
{"curie": "MONDO:0012769", "names": ["HPC14", "PROSTATE CANCER, HEREDITARY, 14", "Prostate Cancer, Hereditary, 14", "prostate cancer, hereditary, 14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate cancer, hereditary, 14", "shortest_name_length": 5}
{"curie": "UMLS:C0030785", "names": ["pelvic abscess", "PELVIC ABSCESS", "abscess pelvic", "Pelvic abscess", "Pelvic Abscess", "pelvis abscess", "PELVIS ABSCESS", "PELVIS, ABSCESS", "abscesses pelvic", "abscess of pelvis", "Pelvic abscess (disorder)", "abscess of pelvis (diagnosis)", "inflammatory disorder abscess of trunk - pelvis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pelvic abscess", "shortest_name_length": 14}
{"curie": "MONDO:0009893", "names": ["PAPA5", "POLYDACTYLY, POSTAXIAL, TYPE A5", "polydactyly, postaxial, type A5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polydactyly, postaxial, type A5", "shortest_name_length": 5}
{"curie": "MONDO:0015678", "names": ["Meyer dysplasia", "Meyer dysplasia of femoral head", "Dysplasia of head of femur Meyer type", "Dysplasia of head of femur, Meyer type", "Dysplasia epiphysealis capitis femoris", "dysplasia of head of femur, Meyer type", "Dysplasia of head of femur Meyer type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dysplasia of head of femur, Meyer type", "shortest_name_length": 15}
{"curie": "MONDO:0018382", "names": ["SufE", "SCFE", "epiphysiolysis of the hip", "femoral head epiphysiolysis", "slipped upper femoral epiphysis", "slipped capital femoral epiphysis", "epiphysiolysis of the upper femur"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epiphysiolysis of the hip", "shortest_name_length": 4}
{"curie": "MONDO:0010785", "names": ["MIDD", "MIDD Syndrome", "Niddm with deafness", "NIDDM with deafness", "NIDDM WITH DEAFNESS", "Mitochondrial Diabetes", "Mitochondrial diabetes", "mitochondrial diabetes", "BALLINGER-WALLACE SYNDROME", "Ballinger-Wallace Syndrome", "Ballinger-Wallace syndrome", "Ballinger Wallace syndrome", "Maternal Diabetes and Deafness Syndrome", "diabetes mellitus type II with deafness", "Diabetes mellitus, type 2, with deafness", "DIABETES MELLITUS, TYPE II, WITH DEAFNESS", "Diabetes Mellitus, Type II, With Deafness", "diabetes mellitus, type II, with deafness", "Maternally inherited diabetes and deafness", "Maternally Inherited Diabetes and Deafness", "Maternally-inherited diabetes and deafness", "maternally inherited diabetes and deafness", "maternally-inherited diabetes and deafness", "DIABETES AND DEAFNESS, MATERNALLY INHERITED", "Diabetes and deafness, maternally inherited", "diabetes and deafness, maternally inherited", "Maternally Transmitted Diabetes with Deafness", "Mitochondrial Inherited Diabetes and Deafness", "Maternally-inherited diabetes and hearing loss", "Diabetes-deafness syndrome maternally transmitted", "Maternally Transmitted Diabetes-Deafness Syndrome", "DIABETES-DEAFNESS SYNDROME, MATERNALLY TRANSMITTED", "Diabetes-deafness syndrome, maternally transmitted", "diabetes-deafness syndrome, maternally Transmitted", "NONINSULIN-DEPENDENT DIABETES MELLITUS WITH DEAFNESS", "noninsulin-dependent diabetes mellitus with deafness", "Noninsulin-dependent diabetes mellitus with deafness", "Diabetes-deafness syndrome maternally transmitted (disorder)", "Diabetes-deafness syndrome maternally transmitted (diagnosis)", "diabetes mellitus associated with genetic syndrome deafness maternally transmitted"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maternally-inherited diabetes and deafness", "shortest_name_length": 4}
{"curie": "MONDO:0008162", "names": ["OMS", "COME/ROM", "come/Rom", "Frequent otitis media", "OTITIS MEDIA RECURRENT", "Otitis media recurrent", "Recurrent otitis media", "Otitis media, frequent", "media otitis recurrent", "recurrent otitis media", "Otitis media, recurrent", "Recurrent middle ear infection", "Susceptibility to otitis media", "OTITIS MEDIA, SUSCEPTIBILITY TO", "OTITIS MEDIA, CHRONIC/RECURRENT", "otitis Media, chronic/recurrent", "otitis media, susceptibility to", "Otitis media, multiple episodes", "Multiple episodes of otitis media", "Recurrent episodes of otitis media", "OTITIS MEDIA, SUSCEPTIBILITY TO (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "otitis media, susceptibility to", "shortest_name_length": 3}
{"curie": "MONDO:0002785", "names": ["Skull Base Tumor", "Skull base tumor", "skull base tumor", "skull base cancer", "Skull base tumour", "basicranium tumor", "Tumor of Skull Base", "Skull Base Neoplasm", "skull base neoplasm", "tumor of skull base", "Skull Base Neoplasms", "tumors of skull base", "tumors of Skull Base", "Neoplasm, Skull Base", "tumor of basicranium", "basicranium neoplasm", "Neoplasms, Skull Base", "neoplasm of skull base", "Neoplasm of Skull Base", "tumor of the skull base", "neoplasm of basicranium", "Tumor of the Skull Base", "Neoplasm of the Skull Base", "neoplasm of the skull base", "basicranium neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skull base neoplasm", "shortest_name_length": 16}
{"curie": "MONDO:0015745", "names": ["microcephaly-polymicrogyria-corpus callosum agenesis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly-polymicrogyria-corpus callosum agenesis syndrome", "shortest_name_length": 61}
{"curie": "UMLS:C0472734", "names": ["Radiation aplastic anemia", "Radiation aplastic anaemia", "Aplastic Anemia due to Radiation", "Aplastic anemia due to radiation", "aplastic anemia due to radiation", "Aplastic anaemia due to radiation", "anemia; aplastic, due to radiation", "aplastic; anemia, due to radiation", "Aplastic anemia caused by radiation", "Aplastic anaemia caused by radiation", "aplastic anemia due to radiation (diagnosis)", "Aplastic anemia caused by radiation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aplastic anemia due to radiation", "shortest_name_length": 25}
{"curie": "MONDO:0044350", "names": ["Hyperparathyroidism, Primary, Caused By Water Clear Cell Hyperplasia", "HYPERPARATHYROIDISM, PRIMARY, CAUSED BY WATER CLEAR CELL HYPERPLASIA", "hyperparathyroidism, primary, caused by water clear cell hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperparathyroidism, primary, caused by water clear cell hyperplasia", "shortest_name_length": 68}
{"curie": "MONDO:0700040", "names": ["neonatal jaundice due to ABO incompatibility", "Neonatal jaundice due to ABO incompatibility", "Neonatal jaundice due to ABO incompatibility (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal jaundice due to ABO incompatibility", "shortest_name_length": 44}
{"curie": "MONDO:0005864", "names": ["Myosarcoma", "myosarcoma", "Myosarcomas", "cancer muscle", "muscle cancer", "Muscle Cancer", "muscle cancers", "Muscle Cancers", "Cancer, Muscle", "cancer muscles", "Muscles--Cancer", "Cancers, Muscle", "Cancer of muscle", "Cancer of Muscle", "cancer of muscle", "cancer of the muscle", "Cancer of the Muscle", "CA - Cancer of muscle", "malignant muscle tumor", "Malignant Muscle Tumor", "myosarcoma (diagnosis)", "muscle structure cancer", "Neoplasm malig;muscle(s)", "Malignant tumor of muscle", "Malignant Muscle Neoplasm", "Malignant muscle neoplasm", "malignant tumor of muscle", "malignant muscle neoplasm", "Malignant Tumor of Muscle", "Malignant tumour of muscle", "cancer of muscle structure", "Malignant neoplasm of muscle", "malignant neoplasm of muscle", "Malignant Neoplasm of Muscle", "Malignant muscle neoplasm NOS", "malignant tumor of the Muscle", "Malignant Tumor of the Muscle", "malignant tumor of the muscle", "Malignant Neoplasm of the Muscle", "malignant neoplasm of the muscle", "Malignant neoplasm of muscle, NOS", "malignant neosplasm of the muscles", "malignant muscle structure neoplasm", "Myosarcoma (morphologic abnormality)", "Malignant tumor of muscle (disorder)", "malignant neoplasm of muscle structure", "malignant neoplasm of muscle (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscle cancer", "shortest_name_length": 10}
{"curie": "UMLS:C1336446", "names": ["stage IV vaginal cancer", "Stage IV Vaginal Cancer", "Stage IV Vaginal Carcinoma", "FIGO Stage IV Vaginal Carcinoma", "Stage IV Vaginal Cancer AJCC v7", "Stage IV Vaginal Cancer AJCC v6", "Stage IV Vaginal Carcinoma AJCC v6", "Stage IV Vaginal Carcinoma AJCC v7", "Stage IV Vaginal Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Vaginal Cancer AJCC v6 and v7", "shortest_name_length": 23}
{"curie": "MONDO:0044638", "names": ["HYPOPHARYNX CANCER SQUAMOUS CELL", "hypopharynx squamous cell carcinoma", "hypopharyngeal epidermoid carcinoma", "epidermoid carcinoma of hypopharynx", "Epidermoid Carcinoma of Hypopharynx", "Hypopharyngeal Epidermoid Carcinoma", "epidermoid carcinoma, hypopharyngeal", "Squamous Cell Carcinoma of Hypopharynx", "hypopharyngeal squamous cell carcinoma", "Hypopharyngeal Squamous Cell Carcinoma", "squamous cell carcinoma of hypopharynx", "squamous cell carcinoma, hypopharyngeal", "Epidermoid Carcinoma of the Hypopharynx", "epidermoid carcinoma of the hypopharynx", "Squamous cell carcinoma of the hypopharynx", "squamous cell carcinoma of the hypopharynx", "hypopharyngeal throat squamous cell cancer", "Squamous Cell Carcinoma of the Hypopharynx", "Hypopharyngeal Throat Squamous Cell Cancer", "squamous cell carcinoma of hypopharynx (diagnosis)", "Hypopharyngeal Conventional Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypopharynx squamous cell carcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C1534903", "names": ["Generalized Arteriosclerosis", "Generalized arteriosclerosis", "Generalised arteriosclerosis", "Generalized arteriosclerotic disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Generalised arteriosclerosis", "shortest_name_length": 28}
{"curie": "UMLS:C0017377", "names": ["Genetic leucocyte disorder", "Genetic leukocyte disorder", "genetic leukocyte anomalies", "Genetic Anomaly of Leukocyte", "Genetic anomaly of leukocyte", "Genetic Anomaly of Leucocyte", "Genetic anomaly of leucocyte", "Congenital Leukocyte Anomaly", "Congenital Leucocyte Anomaly", "Genetic anomalies of leucocytes", "Genetic anomalies of leukocytes", "Congenital Leukocyte Abnormality", "Congenital Leucocyte Abnormality", "Genetic anomaly of leukocyte, NOS", "genetic leukocyte anomalies (diagnosis)", "Genetic anomaly of leukocyte (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Genetic anomaly of leukocyte", "shortest_name_length": 26}
{"curie": "MONDO:0013827", "names": ["HKPX3", "HYPEREKPLEXIA 3", "hyperekplexia 3", "hyperekplexia type 3", "SLC6A5 hereditary hyperekplexia", "hereditary hyperekplexia caused by mutation in SLC6A5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperekplexia 3", "shortest_name_length": 5}
{"curie": "MONDO:0014404", "names": ["WEDAS", "Webb-Dattani syndrome", "WEBB-Dattani syndrome", "WEBB-DATTANI SYNDROME", "hypothalamo-pituitary-frontotemporal hypoplasia with visual and renal anomalies", "HYPOTHALAMO-PITUITARY-FRONTOTEMPORAL HYPOPLASIA WITH VISUAL AND RENAL ANOMALIES", "hypothalamic insufficiency-secondary microcephaly-visual impairment-urinary anomalies syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Webb-Dattani syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0855005", "names": ["Stage IV Lung Cancer", "lung cancer stage iv", "stage iv lung cancer", "cancer iv lung stage", "Lung cancer stage IV", "Cancer of lung stage IV", "Lung carcinoma stage IV", "Carcinoma of lung stage IV", "Stage IV Lung Cancer AJCC v7", "Pulmonary carcinoma stage IV", "Lung cancer cell type unspecified stage IV", "Lung carcinoma cell type unspecified stage IV", "Cancer of lung cell type unspecified stage IV", "Carcinoma of lung cell type unspecified stage IV", "Pulmonary carcinoma cell type unspecified stage IV"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Lung Cancer AJCC v7", "shortest_name_length": 20}
{"curie": "MONDO:0020729", "names": ["AGM1", "agammaglobulinemia 1", "autosomal recessive agammaglobulinemia 1", "AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE", "agammaglobulinemia 1, autosomal recessive", "agammaglobulinemia, autosomal recessive, due to IGHM defect", "AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO IGHM DEFECT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive agammaglobulinemia 1", "shortest_name_length": 4}
{"curie": "MONDO:0014316", "names": ["AD19", "ALZHEIMER DISEASE 19", "Alzheimer disease 19", "PLD3 Alzheimer disease", "Alzheimer's disease 19", "Alzheimer disease type 19", "Alzheimer's disease type 19", "Alzheimer disease 19 late onset", "Alzheimer disease 19, late-onset", "ALZHEIMER DISEASE 19, LATE-ONSET", "Alzheimer disease caused by mutation in PLD3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alzheimer disease 19", "shortest_name_length": 4}
{"curie": "MONDO:0060631", "names": ["ALKKUCS", "ALKURAYA-KUCINSKAS SYNDROME", "Alkuraya-Kucinskas syndrome", "KIAA1109-related early lethal congenital brain malformations-arthrogryposis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alkuraya-Kucinskas syndrome", "shortest_name_length": 7}
{"curie": "UMLS:C1336245", "names": ["stage III extragonadal non-seminomatous germ cell tumor", "Stage III Extragonadal Non-Seminomatous Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Extragonadal Non-Seminomatous Germ Cell Tumor", "shortest_name_length": 55}
{"curie": "MONDO:0000070", "names": ["mycobacterium tuberculosis, susceptibility"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mycobacterium tuberculosis, susceptibility", "shortest_name_length": 42}
{"curie": "MONDO:0002669", "names": ["ampullary signet Ring cell carcinoma", "Ampullary Signet Ring Cell Carcinoma", "ampullary signet ring cell carcinoma", "ampullary signet ring cell adenocarcinoma", "Ampulla of Vater Signet Ring Cell Carcinoma", "ampulla of Vater signet Ring cell carcinoma", "Ampulla of Vater Signet-Ring Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ampullary signet ring cell adenocarcinoma", "shortest_name_length": 36}
{"curie": "MONDO:0010836", "names": ["NNO1", "NANOPHTHALMIA 1", "nanophthalmos 1", "Nanophthalmia 1", "nanophthalmos-1", "NANOPHTHALMOS 1", "Nanophthalmos 1", "Nanophthalmos, Autosomal Dominant", "NANOPHTHALMOS, AUTOSOMAL DOMINANT", "nanophthalmos, autosomal dominant", "MICROPHTHALMOS, SIMPLE, AUTOSOMAL DOMINANT", "microphthalmos, simple, autosomal dominant", "Microphthalmos, Simple, Autosomal Dominant", "nanophthalmos with high hyperopia and angle-closure glaucoma", "NANOPHTHALMOS WITH HIGH HYPEROPIA AND ANGLE-CLOSURE GLAUCOMA", "Nanophthalmos with High Hyperopia and Angle-Closure Glaucoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nanophthalmos 1", "shortest_name_length": 4}
{"curie": "UMLS:C4727194", "names": ["Locally Advanced Small Intestinal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Small Intestinal Carcinoma", "shortest_name_length": 43}
{"curie": "UMLS:C4520745", "names": ["Lip and Oral Cavity Cancer Stage II", "Stage II Lip and Oral Cavity Cancer", "stage II lip and oral cavity cancer", "Stage II Lip and Oral Cavity Carcinoma", "Lip and Oral Cavity Carcinoma Stage II", "Stage II Lip and Oral Cavity Cancer AJCC v7", "Stage II Lip and Oral Cavity Cancer AJCC v6", "Stage II Lip and Oral Cavity Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Lip and Oral Cavity Cancer AJCC v6 and v7", "shortest_name_length": 35}
{"curie": "MONDO:0020195", "names": ["excretory apparatus of the lacrimal system anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "excretory apparatus of the lacrimal system anomaly", "shortest_name_length": 50}
{"curie": "MONDO:0024673", "names": ["skin lymphangioma", "Lymphangioma;skin", "Skin Lymphangioma", "Lymphangioma of skin", "Cutaneous Lymphangioma", "cutaneous lymphangioma", "lymphangioma of the skin", "Lymphangioma of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin lymphangioma", "shortest_name_length": 17}
{"curie": "MONDO:0014002", "names": ["ENFL5", "nocturnal frontal lobe epilepsy 5", "epilepsy nocturnal frontal lobe, 5", "EPILEPSY, NOCTURNAL FRONTAL LOBE, 5", "epilepsy, nocturnal frontal lobe, 5", "epilepsy, nocturnal frontal lobe, type 5", "autosomal dominant nocturnal frontal lobe epilepsy 5", "KCNT1 autosomal dominant nocturnal frontal lobe epilepsy", "autosomal dominant nocturnal frontal lobe epilepsy type 5", "autosomal dominant nocturnal frontal lobe epilepsy caused by mutation in KCNT1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nocturnal frontal lobe epilepsy 5", "shortest_name_length": 5}
{"curie": "UMLS:C0855249", "names": ["Sleep disorder due to general medical condition, insomnia type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sleep disorder due to general medical condition, insomnia type", "shortest_name_length": 62}
{"curie": "UMLS:C5205966", "names": ["Seminal Vesicle Schwannoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Seminal Vesicle Schwannoma", "shortest_name_length": 26}
{"curie": "MONDO:0030912", "names": ["MRD47", "autosomal dominant mental retardation 47", "mental retardation, autosomal dominant 47", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 47", "autosomal dominant intellectual disability 47", "intellectual disability, autosomal dominant 47", "autosomal dominant intellectual developmental disorder 47", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 47", "STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 47", "shortest_name_length": 5}
{"curie": "MONDO:0045019", "names": ["lactation disease", "Lactation disorder", "Disorder;lactation", "Lactation Disorder", "LACTATION DISORDER", "lactation disorder", "Lactation Disorders", "Lactation disorders", "lactation; disorder", "disorder; lactation", "Disorder, Lactation", "Disorders, Lactation", "Disorder of lactation", "DISORDER OF LACTATION", "disorder of lactation", "Lactation disorder NOS", "Disorder of lactation, NOS", "lactation disorder (diagnosis)", "Disorder of lactation (disorder)", "Unspecified disorder of lactation", "Unspecified disorders of lactation", "Unspecified disorder of lactation, unspecified as to episode of care", "Unspecified disorder of lactation, unspecified as to episode of care or not applicable"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lactation disease", "shortest_name_length": 17}
{"curie": "UMLS:C1709247", "names": ["Non-Neoplastic Disease by Site", "Non-Neoplastic Disorder by Site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Disorder by Site", "shortest_name_length": 30}
{"curie": "MONDO:0024893", "names": ["Toxocara canis infection (canine roundworms)", "Toxocara catis infection (feline roundworms)", "toxocara canis infection (canine roundworms)", "Human infection with the larvae of canine or feline roundworms"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "toxocara canis infection (canine roundworms)", "shortest_name_length": 44}
{"curie": "MONDO:0034145", "names": ["OCSKD", "oculocerebrodental syndrome", "oculoskeletodental syndrome", "Oculocerebrodental syndrome", "OCULOSKELETODENTAL SYNDROME", "Oculo-cerebro-dental syndrome", "Oculocerebrodental syndrome (disorder)", "CATARACTS, EARLY-ONSET, WITH SKELETAL AND DENTAL ANOMALIES", "Cataracts, Early-Onset, With Skeletal and Dental Anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculocerebrodental syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0589110", "names": ["Postoperative deep vein thrombosis", "Deep vein thrombosis postoperative", "postoperative deep venous thrombosis", "venous thrombosis deep postoperative", "Postoperative deep vein thrombosis (disorder)", "postoperative deep venous thrombosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postoperative deep vein thrombosis", "shortest_name_length": 34}
{"curie": "MONDO:0037739", "names": ["Benign neoplasm of cauda equina", "benign neoplasm of cauda equina", "Benign neoplasm of cauda equina (disorder)", "benign neoplasm of cauda equina (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of cauda equina", "shortest_name_length": 31}
{"curie": "UMLS:C0240066", "names": ["Sideropenia", "Sideropenias", "iron deficiency", "Iron Deficiency", "Deficiency;iron", "deficiency iron", "IRON DEFICIENCY", "Iron deficiency", "Deficiency, Iron", "iron; deficiency", "deficiency; iron", "iron deficiencies", "Iron Deficiencies", "Iron deficiencies", "Deficiencies, Iron", "Iron deficiency, NOS", "Iron deficiency (disorder)", "iron deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Iron deficiency", "shortest_name_length": 11}
{"curie": "MONDO:0011459", "names": ["ARVD5", "ARVC5", "arrhythmogenic right ventricular dysplasia 5", "arrhythmogenic right ventricular cardiomyopathy 5", "ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 5", "arrhythmogenic right ventricular dysplasia type 5", "Arrhythmogenic Right Ventricular Cardiomyopathy 5", "familial arrhythmogenic right ventricular dysplasia 5", "Familial Arrhythmogenic Right Ventricular Dysplasia 5", "TMEM43 arrhythmogenic right ventricular cardiomyopathy", "ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 5", "Arrhythmogenic Right Ventricular Dysplasia, Familial, 5", "arrhythmogenic right ventricular dysplasia, familial, 5", "arrhythmogenic right ventricular dysplasia, familial, type 5", "arrhythmogenic right ventricular cardiomyopathy caused by mutation in TMEM43"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arrhythmogenic right ventricular dysplasia 5", "shortest_name_length": 5}
{"curie": "MONDO:0100464", "names": ["acid sphingomyelinase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acid sphingomyelinase deficiency", "shortest_name_length": 32}
{"curie": "UMLS:C2981277", "names": ["Stage IVB Thyroid Gland Anaplastic Carcinoma AJCC v7", "Undifferentiated (Anaplastic) Stage IVB Thyroid Gland Cancer", "Stage IVB Thyroid Gland Undifferentiated (Anaplastic) Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Thyroid Gland Undifferentiated (Anaplastic) Carcinoma AJCC v7", "shortest_name_length": 52}
{"curie": "MONDO:0012834", "names": ["SLEB10", "IRF5 systemic lupus erythematosus (disease)", "susceptibility to systemic lupus erythematosus 10", "systemic lupus erythematosus, susceptibility to, 10", "SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 10", "systemic lupus erythematosus, susceptibility to, type 10", "SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 10 (finding)", "systemic lupus erythematosus (disease) caused by mutation in IRF5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "systemic lupus erythematosus, susceptibility to, 10", "shortest_name_length": 6}
{"curie": "UMLS:C4526966", "names": ["Stage IA Gastric and Omental GIST AJCC v8", "Stage IA Gastric and Omental Gastrointestinal Stromal Tumor AJCC v8", "Stage IA Gastric (Stomach) and Omental Gastrointestinal Stromal Tumor (GIST)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Gastric and Omental Gastrointestinal Stromal Tumor AJCC v8", "shortest_name_length": 41}
{"curie": "UMLS:C4552678", "names": ["Stage I Renal Pelvis Cancer", "Stage I Renal Pelvis Cancer AJCC v8", "Stage I Renal Pelvis Urothelial Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Renal Pelvis Cancer AJCC v8", "shortest_name_length": 27}
{"curie": "MONDO:0021222", "names": ["lacrimal gland tumor", "Lacrimal Gland Neoplasm", "lacrimal gland neoplasm", "tumor of lacrimal gland", "Neoplasm of Lacrimal Gland", "neoplasm of lacrimal gland", "tumor of the lacrimal gland", "Neoplasm of the Lacrimal Gland", "neoplasm of the lacrimal gland", "lacrimal gland neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lacrimal gland neoplasm", "shortest_name_length": 20}
{"curie": "UMLS:C5237226", "names": ["Reserve Cell Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reserve Cell Hyperplasia", "shortest_name_length": 24}
{"curie": "MONDO:0010698", "names": ["OPA2", "OPTIC ATROPHY 2", "Optic atrophy 2", "optic atrophy 2", "Optic atrophy type 2", "optic atrophy type 2", "Optic atrophy, X-linked", "OPTIC ATROPHY, X-LINKED", "optic atrophy, X-linked", "X-linked optic atrophy 2", "optic atrophy 2, X-linked", "OPTIC ATROPHY 2 (disorder)", "Early-onset X-linked optic atrophy", "Non-Leber type optic atrophy with early-onset", "Early-onset X-linked optic atrophy (disorder)", "non-Leber type optic atrophy with early-onset", "optic atrophy, non-Leber type, with early onset", "Optic atrophy, non-Leber type, with early onset", "OPTIC ATROPHY, NON-LEBER TYPE, WITH EARLY ONSET"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "optic atrophy 2", "shortest_name_length": 4}
{"curie": "MONDO:0011923", "names": ["OS3", "ASPN osteoarthritis", "osteoarthritis of knee/hip", "OSTEOARTHRITIS OF KNEE/HIP", "OSTEOARTHRITIS SUSCEPTIBILITY 3", "osteoarthritis susceptibility 3", "osteoarthritis susceptibility type 3", "osteoarthritis caused by mutation in ASPN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteoarthritis susceptibility 3", "shortest_name_length": 3}
{"curie": "MONDO:0002697", "names": ["GBY", "gonadoblastoma", "ovary gonadoblastoma", "Ovarian gonadoblastoma", "Ovarian Gonadoblastoma", "Gonadoblastoma, female", "ovarian gonadoblastoma", "gonadoblastoma of ovary", "Gonadoblastoma of ovary", "ovarian gonadoblastoma (disease)", "Gonadoblastoma of ovary (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian gonadoblastoma", "shortest_name_length": 3}
{"curie": "MONDO:0030839", "names": ["THMA2", "THYROID HORMONE METABOLISM, ABNORMAL, 2", "thyroid hormone metabolism, abnormal, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid hormone metabolism, abnormal, 2", "shortest_name_length": 5}
{"curie": "MONDO:0030844", "names": ["SPGF47", "spermatogenic failure 47", "SPERMATOGENIC FAILURE 47"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 47", "shortest_name_length": 6}
{"curie": "MONDO:0013211", "names": ["CMD1FF", "dilated cardiomyopathy 1FF", "cardiomyopathy, dilated, 1FF", "Cardiomyopathy, Dilated, 1FF", "CARDIOMYOPATHY, DILATED, 1FF", "dilated cardiomyopathy type 1FF", "cardiomyopathy, dilated, type 1Ff"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1FF", "shortest_name_length": 6}
{"curie": "MONDO:0032888", "names": ["NEDBAVC", "neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies", "NEURODEVELOPMENTAL DISORDER WITH BRAIN ANOMALIES AND WITH OR WITHOUT VERTEBRAL OR CARDIAC ANOMALIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies", "shortest_name_length": 7}
{"curie": "UMLS:C1516436", "names": ["Cervical Warty Carcinoma", "Cervical Warty Squamous Cell Carcinoma", "Cervical Condylomatous Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Warty Carcinoma", "shortest_name_length": 24}
{"curie": "UMLS:C0553767", "names": ["cerebral palsy congenital", "Congenital cerebral palsy", "Congenital Cerebral Palsy", "Cerebral Palsy, Congenital", "Cerebral palsy, congenital", "Congenital cerebral palsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Cerebral Palsy", "shortest_name_length": 25}
{"curie": "UMLS:C0155624", "names": ["Unspecified renovascular hypertension", "Unspecified Renovascular Hypertension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unspecified renovascular hypertension", "shortest_name_length": 37}
{"curie": "UMLS:C1697542", "names": ["Infusion site thrombosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infusion site thrombosis", "shortest_name_length": 24}
{"curie": "UMLS:C5239505", "names": ["Locally Advanced Breast Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Breast Adenocarcinoma", "shortest_name_length": 38}
{"curie": "UMLS:C2987165", "names": ["Hepatoid carcinoma", "Pancreatic Hepatoid Carcinoma", "Pancreatic Hepatoid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Hepatoid Adenocarcinoma", "shortest_name_length": 18}
{"curie": "MONDO:0008387", "names": ["RDC", "Ring dermoid syndrome", "ring dermoid syndrome", "Ring dermoid of cornea", "RING DERMOID OF CORNEA", "ring dermoid of cornea", "RING dermoid of cornea", "Ring dermoid of cornea (disorder)", "Bilateral, annular limbal dermoids with corneal and conjunctival extension", "bilateral, annular limbal dermoids with corneal and conjunctival extension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ring dermoid of cornea", "shortest_name_length": 3}
{"curie": "UMLS:C4683010", "names": ["stage 0 eyelid carcinoma", "Stage 0 Eyelid Carcinoma AJCC v8", "stage 0 eyelid carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Eyelid Carcinoma AJCC v8", "shortest_name_length": 24}
{"curie": "MONDO:0017512", "names": ["split hand, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "split hand, bilateral", "shortest_name_length": 21}
{"curie": "MONDO:0008673", "names": ["WAD", "wad", "CURRY-HALL SYNDROME", "Curry Hall syndrome", "Curry-Hall syndrome", "curry Hall syndrome", "curry-Hall syndrome", "Weyers acrodental dysostosis", "WEYERS ACRODENTAL DYSOSTOSIS", "Weyers acrofacial dysostosis", "WEYERS ACROFACIAL DYSOSTOSIS", "Curry-Hall syndrome (disorder)", "acrofacial dysostosis of Weyers", "acrodental dysostosis of Weyers", "Acrodental dysostosis of Weyers", "ACRODENTAL DYSOSTOSIS OF WEYERS", "Acrofacial dysostosis of Weyers", "Acrofacial dysostosis Weyers type", "acrofacial dysostosis, Weyers type", "Acrofacial dysostosis, Weyers type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acrofacial dysostosis, Weyers type", "shortest_name_length": 3}
{"curie": "MONDO:0005347", "names": ["elevated tg", "Hyperglyceridemia", "hyperglyceridemia", "Hyperglyceridaemia", "high triglycerides", "hyperglyceridaemia", "Hypertriglyceridemia", "hypertriglyceridemia", "HYPERTRIGLYCERIDEMIA", "Hypertriglyceridaemia", "HYPERTRIGLYCERIDAEMIA", "Hypertriglyceridemias", "hypertriglyceridaemia", "Elevated triglycerides", "elevated triglycerides", "increased triglycerides", "hypertriglyceridemia (disease)", "Hypertriglyceridemia (disorder)", "hypertriglyceridemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertriglyceridemia", "shortest_name_length": 11}
{"curie": "UMLS:C5446454", "names": ["Lacrimal Drainage System Lymphoepithelial Carcinoma", "Lacrimal Drainage System Lymphoepithelioma-Like Carcinoma", "Lymphoepithelial Carcinoma of the Lacrimal Drainage System", "Lymphoepithelioma-Like Carcinoma of the Lacrimal Drainage System", "Non-Keratinizing Undifferentiated Nasopharyngeal-Type Carcinoma of the Lacrimal Drainage System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lacrimal Drainage System Lymphoepithelial Carcinoma", "shortest_name_length": 51}
{"curie": "UMLS:C0002793", "names": ["Anaplasia", "anaplasia", "Anaplasias", "Dedifferentiation", "dedifferentiation", "Anaplastic Lesion", "Anaplastic Change", "Dedifferentiation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anaplasia", "shortest_name_length": 9}
{"curie": "MONDO:0003867", "names": ["diffuse melanosis", "Diffuse melanosis", "Diffuse Melanosis", "diffuse melanocytosis", "Diffuse Melanocytosis", "Diffuse melanocytosis", "meningeal melanocytosis", "Meningeal melanocytosis", "Meningeal Melanocytosis", "Diffuse Meningeal Melanocytosis", "diffuse meningeal melanocytosis", "Diffuse melanosis (morphologic abnormality)", "Diffuse melanocytosis (morphologic abnormality)", "diffuse melanocytosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diffuse meningeal melanocytosis", "shortest_name_length": 17}
{"curie": "UMLS:C0339805", "names": ["cat allergy", "Cat Allergy", "Cat allergy", "allergy cat", "cats allergy", "allergy cats", "Allergy, Cat", "allergies cat", "allergies cats", "allergy to cats", "ALLERGY TO CATS", "Allergic to cats", "allergic to cats", "Cat allergy (disorder)", "Allergy to Felis catus protein", "Allergy to domestic cat protein", "Allergy to Felis catus protein (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cat allergy (disorder)", "shortest_name_length": 11}
{"curie": "MONDO:0018808", "names": ["Caroli syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Caroli syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0033642", "names": ["BABS", "NEDABA", "BACHMANN-BUPP SYNDROME", "Bachmann Bupp syndrome", "Bachmann-Bupp syndrome", "Ornithine decarboxylase deficiency", "neurodevelopmental disorder with alopecia and brain abnormalities", "NEURODEVELOPMENTAL DISORDER WITH ALOPECIA AND BRAIN ABNORMALITIES", "global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome", "Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome", "Global developmental delay, alopecia, macrocephaly, facial dysmorphism, structural brain anomalies syndrome", "Global developmental delay, alopecia, macrocephaly, facial dysmorphism, structural brain anomalies syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with alopecia and brain abnormalities", "shortest_name_length": 4}
{"curie": "UMLS:C4528203", "names": ["Nodal Peripheral T-Cell Lymphoma of TFH Cell Origin", "Nodal Peripheral T-Cell Lymphoma of T Follicular Helper Cell Origin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nodal Peripheral T-Cell Lymphoma of T Follicular Helper Cell Origin", "shortest_name_length": 51}
{"curie": "MONDO:0021092", "names": ["Fallopian tube Ca", "fallopian tube tumor", "Fallopian Tube Tumor", "Fallopian Tube Cancer", "fallopian tube tumors", "FALLOPIAN TUBE CANCER", "fallopian tube cancer", "Fallopian tube cancer", "Fallopian Tube Cancers", "Cancer, Fallopian Tube", "Fallopian tube neoplasm", "Tumor of Fallopian Tube", "tumor of fallopian tube", "Cancers, Fallopian Tube", "fallopian tube neoplasm", "Fallopian Tube Neoplasm", "Tumor of fallopian tube", "Neoplasm, Fallopian Tube", "Tumour of fallopian tube", "fallopian tube neoplasms", "Fallopian tube carcinoma", "fallopian tube carcinoma", "Cancer of Fallopian Tube", "Fallopian Tube Neoplasms", "Fallopian Tube Carcinoma", "FALLOPIAN TUBE, CARCINOMA", "Neoplasms, Fallopian Tube", "Fallopian tube cancer NOS", "Neoplasm of fallopian tube", "Neoplasm of Fallopian Tube", "neoplasm of fallopian tube", "Carcinoma of fallopian tube", "Carcinoma of Fallopian Tube", "Fallopian tube neoplasm NOS", "carcinoma of fallopian tube", "Tumor of the Fallopian Tube", "tumor of the fallopian tube", "Cancer of the Fallopian Tube", "cancer of the fallopian tube", "neoplasm of the fallopian tube", "Neoplasm of the Fallopian Tube", "Carcinoma of the Fallopian Tube", "FALLOPIAN TUBE CANCER, CARCINOMA", "fallopian tube neoplasm (disease)", "Neoplasm of fallopian tube (disorder)", "Carcinoma of fallopian tube (disorder)", "neoplasm of fallopian tube (diagnosis)", "carcinoma of fallopian tube (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fallopian tube neoplasm", "shortest_name_length": 17}
{"curie": "MONDO:0018089", "names": ["DORV", "Taussig-Bing defect", "Taussig-Bing syndrome", "dextrotransposition; aortic", "Dextratransposition of aorta", "Dextrotransposition of aorta", "Double outlet right ventricle", "DOUBLE-OUTLET RIGHT VENTRICLE", "Double-Outlet Right Ventricle", "Double-outlet right ventricle", "Double Outlet Right Ventricle", "double outlet right ventricle", "DOUBLE OUTLET RIGHT VENTRICLE", "Double-Outlet Right Ventricles", "ventricle; double outlet right", "double right ventricle; outlet", "Right Ventricle, Double-Outlet", "Ventricle, Double-Outlet Right", "outlet; double right ventricle", "ventricle; right, double outlet", "Taussig-Bing syndrome or defect", "double; outlet, right ventricle", "double outlet of right ventricle", "Double outlet right ventricle (DORV)", "DORV - Double outlet right ventricle", "Dextrotransposition of aorta (disorder)", "Double outlet right ventricle (disorder)", "Origin of great vessels from right ventricle", "double outlet of right ventricle (diagnosis)", "Origin of both great vessels from right ventricle", "Double outlet right ventricle with subpulmonary ventricular septal defect", "Transposition of great vessels, interventricular septal defect AND overriding aorta", "Transposition of great vessels, interventricular septal defect and overriding aorta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "double outlet right ventricle", "shortest_name_length": 4}
{"curie": "MONDO:0007378", "names": ["PPCD", "PPCD1", "Ppcd1", "Ched1", "CHED1, FORMERLY", "Schlichting dystrophy", "MAUMENEE CORNEAL DYSTROPHY", "Maumenee Corneal Dystrophy", "Maumenee corneal dystrophy", "Polymorphous corneal dystrophy", "Posterior polymorphous dystrophy", "corneal dystrophy posterior polymorphous", "Posterior polymorphous corneal dystrophy", "Polymorphous posterior corneal dystrophy", "Posterior Polymorphous Corneal Dystrophy", "posterior polymorphous corneal dystrophy", "POSTERIOR POLYMORPHOUS CORNEAL DYSTROPHY", "posterior polymorphous corneal dystrophy 1", "corneal dystrophy, POSTERIOR polymorphous, 1", "Corneal Dystrophy, Posterior Polymorphous, 1", "CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 1", "posterior polymorphous corneal dystrophy type 1", "Ppcd1 Posterior polymorphous corneal dystrophy 1", "corneal dystrophy, posterior polymorphous, type 1", "Posterior polymorphous corneal dystrophy (disorder)", "corneal endothelial dystrophy 1, autosomal dominant", "Corneal Endothelial Dystrophy 1, Autosomal Dominant", "CORNEAL ENDOTHELIAL DYSTROPHY 1, AUTOSOMAL DOMINANT", "Corneal Dystrophy, Hereditary Polymorphous Posterior", "CORNEAL DYSTROPHY, HEREDITARY POLYMORPHOUS POSTERIOR", "Posterior polymorphous corneal dystrophy (diagnosis)", "corneal dystrophy, hereditary polymorphous posterior", "CORNEAL ENDOTHELIAL DYSTROPHY 1, AUTOSOMAL DOMINANT, FORMERLY", "corneal endothelial dystrophy 1, autosomal dominant, formerly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "posterior polymorphous corneal dystrophy 1", "shortest_name_length": 4}
{"curie": "MONDO:0012354", "names": ["BDPLT8", "P2Y12 defect", "platelet-type bleeding disorder 8", "bleeding disorder, platelet-type 8", "ADP platelet receptor P2Y12 defect", "bleeding disorder, platelet-type, 8", "BLEEDING DISORDER, PLATELET-TYPE, 8", "BLEEDING DISORDER DUE TO P2RY12 DEFECT", "bleeding disorder due to P2Ry12 defect", "Bleeding Disorder Due To P2RY12 Defect", "bleeding disorder due to P2Rx1 defect, somatic", "Defect of purinergic receptor p2y G protein-coupled 12", "P2Y12 (purinergic receptor p2y G protein-coupled 12) defect", "Defect of purinergic receptor p2y G protein-coupled 12 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "platelet-type bleeding disorder 8", "shortest_name_length": 6}
{"curie": "MONDO:0013887", "names": ["HTX6", "heterotaxy, visceral, 6, autosomal", "HETEROTAXY, VISCERAL, 6, AUTOSOMAL", "heterotaxy, visceral, 6, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heterotaxy, visceral, 6, autosomal", "shortest_name_length": 4}
{"curie": "MONDO:0023017", "names": ["duplication of the thumb unilateral biphalangeal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "duplication of the thumb unilateral biphalangeal", "shortest_name_length": 48}
{"curie": "MONDO:0002672", "names": ["Prostate Signet Ring Cell Carcinoma", "prostate signet Ring cell carcinoma", "prostate signet ring cell carcinoma", "Signet Ring cell carcinoma of prostate", "signet Ring cell carcinoma of prostate", "Signet Ring Cell Carcinoma of Prostate", "prostate signet ring cell adenocarcinoma", "prostate gland signet ring cell carcinoma", "signet Ring cell carcinoma of the prostate", "Signet Ring Cell Carcinoma of the Prostate", "Acinar Prostate Adenocarcinoma, Signet Ring Variant", "acinar prostate adenocarcinoma, signet ring variant", "Prostate Acinar Adenocarcinoma, Signet Ring Variant", "acinar prostate adenocarcinoma, signet Ring variant", "Prostate Acinar Adenocarcinoma, Signet Ring-Like Cell Variant", "Prostate Acinar Adenocarcinoma, Signet-Ring-Like Cell Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acinar prostate adenocarcinoma, signet ring variant", "shortest_name_length": 35}
{"curie": "MONDO:0004047", "names": ["sphenoid sinus tumor", "Sphenoid Sinus Tumor", "Sphenoidal Sinus Tumor", "sphenoidal sinus tumor", "Tumor of Sphenoid Sinus", "Tumor of sphenoid sinus", "tumor of sphenoid sinus", "sphenoid sinus neoplasm", "Sphenoid Sinus Neoplasm", "Tumour of sphenoid sinus", "tumor of Sphenoidal sinus", "Sphenoidal Sinus Neoplasm", "sphenoidal sinus neoplasm", "Tumor of Sphenoidal Sinus", "tumor of sphenoidal sinus", "Neoplasm of Sphenoid Sinus", "neoplasm of sphenoid sinus", "tumor of the sphenoid sinus", "Tumor of the Sphenoid Sinus", "Neoplasm of Sphenoidal Sinus", "Neoplasm of sphenoidal sinus", "neoplasm of sphenoidal sinus", "tumor of the sphenoidal sinus", "Tumor of the Sphenoidal Sinus", "neoplasm of the sphenoid sinus", "Neoplasm of the Sphenoid Sinus", "neoplasm of the sphenoidal sinus", "Neoplasm of the Sphenoidal Sinus", "sphenoidal sinus benign neoplasm", "sphenoidal sinus neoplasm (disease)", "neoplasm of sphenoid sinus (diagnosis)", "Neoplasm of sphenoidal sinus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sphenoidal sinus neoplasm", "shortest_name_length": 20}
{"curie": "MONDO:0045047", "names": ["neurosarcoidosis", "Neurosarcoidosis", "NEUROSARCOIDOSIS", "Nervous system sarcoidosis", "nervous system sarcoidosis", "Neurosarcoidosis (disorder)", "sarcoidosis of nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurosarcoidosis", "shortest_name_length": 16}
{"curie": "UMLS:C4682576", "names": ["Stage IVA Uterine Corpus Endometrial Stromal Sarcoma", "Stage IVA Uterine Corpus Endometrial Stromal Sarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Uterine Corpus Endometrial Stromal Sarcoma AJCC v8", "shortest_name_length": 52}
{"curie": "MONDO:0003594", "names": ["Mixed liposarcoma", "mixed liposarcoma", "Mixed Liposarcoma", "Mixed-type liposarcoma", "mixed liposarcoma (morphologic abnormality)", "Mixed liposarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed liposarcoma", "shortest_name_length": 17}
{"curie": "MONDO:0013841", "names": ["STUT3", "STUTTERING, FAMILIAL PERSISTENT, 3", "stuttering, familial persistent, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stuttering, familial persistent, 3", "shortest_name_length": 5}
{"curie": "MONDO:0001783", "names": ["Stromal nodule", "Endometrial stromal nodule", "Endometrial Stromal Nodule", "endometrial stromal nodule", "[M] Endometrial stromal nodule", "Benign endometrial stromal neoplasm", "Benign endometrial stromal neoplasm (disorder)", "Endometrial stromal nodule (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometrial stromal nodule", "shortest_name_length": 14}
{"curie": "MONDO:0100271", "names": ["PEX26 related Zellweger spectrum disorder", "peroxisome biogenesis disorder due to PEX26 defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder due to PEX26 defect", "shortest_name_length": 41}
{"curie": "UMLS:C2987242", "names": ["Nonfunctional Pancreatic Neuroendocrine Tumor G1", "Non-Functional Pancreatic Neuroendocrine Tumor G1", "Nonfunctioning Pancreatic Neuroendocrine Tumor G1", "Non-Functioning Pancreatic Neuroendocrine Tumor G1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Functioning Pancreatic Neuroendocrine Tumor G1", "shortest_name_length": 48}
{"curie": "UMLS:C0333876", "names": ["Columnar cell atypia", "Columnar Cell Atypia", "Atypia, columnar cell", "Columnar cell atypia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Columnar cell atypia", "shortest_name_length": 20}
{"curie": "UMLS:C5555154", "names": ["Bone Rosai-Dorfman Disease", "Bone Sinus Histiocytosis with Massive Lymphadenopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone Rosai-Dorfman Disease", "shortest_name_length": 26}
{"curie": "MONDO:0005102", "names": ["UES", "Embryonal Sarcoma", "embryonal sarcoma", "Embryonal sarcoma", "embryonal; sarcoma", "sarcoma; embryonal", "Liver Embryonal Sarcoma", "Undifferentiated sarcoma", "undifferentiated sarcoma", "Undifferentiated Sarcoma", "embryonal sarcoma (diagnosis)", "Embryonal Sarcoma of the Liver", "embryonal sarcoma, undifferentiated", "undifferentiated (embryonal) sarcoma", "undifferentiated sarcoma (diagnosis)", "Undifferentiated (Embryonal) Sarcoma", "sarcoma, undifferentiated, malignant", "Embryonal sarcoma (morphologic abnormality)", "Embryonal Sarcoma (Undifferentiated Sarcoma)", "embryonal sarcoma (undifferentiated sarcoma)", "Undifferentiated sarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "undifferentiated (embryonal) sarcoma", "shortest_name_length": 3}
{"curie": "MONDO:0014705", "names": ["CRS6", "craniosynostosis 6", "CRANIOSYNOSTOSIS 6", "ZIC1 craniosynostosis", "craniosynostosis type 6", "craniosynostosis caused by mutation in ZIC1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniosynostosis 6", "shortest_name_length": 4}
{"curie": "MONDO:0005034", "names": ["FTC", "carcinoma follicular", "Follicular Carcinoma", "follicular carcinoma", "Follicular carcinoma", "FOLLICULAR CARCINOMA", "carcinomas follicular", "Thyroid adenocarcinoma", "adenocarcinoma thyroid", "Follicular Thyroid Cancer", "thyroid follicular cancer", "cancer follicular thyroid", "Follicular Adenocarcinoma", "Follicular carcinoma, NOS", "follicular thyroid cancer", "Follicular adenocarcinoma", "follicular adenocarcinoma", "Adenocarcinoma, Follicular", "Follicular Adenocarcinomas", "thyroid follicle carcinoma", "Adenocarcinomas, Follicular", "carcinoma; follicular, pure", "follicular cancer of thyroid", "Follicular Cancer of Thyroid", "thyroid follicular carcinoma", "follicular carcinoma thyroid", "follicular thyroid carcinoma", "carcinoma follicular thyroid", "Follicular Thyroid Carcinoma", "thyroid gland adenocarcinoma", "Follicular thyroid carcinoma", "Thyroid Follicular Carcinoma", "THYROID FOLLICULAR CARCINOMA", "carcinoma of thyroid follicle", "Follicular Thyroid Carcinomas", "THYROID CARCINOMA, FOLLICULAR", "Follicular adenocarcinoma NOS", "Carcinoma, Follicular Thyroid", "Thyroid Carcinoma, Follicular", "Carcinomas, Follicular Thyroid", "Thyroid Carcinomas, Follicular", "Follicular adenocarcinoma, NOS", "THYROID, CARCINOMA, FOLLICULAR", "Thyroid Gland Follicular Cancer", "thyroid gland follicular cancer", "Follicular Carcinoma of Thyroid", "follicular carcinoma of thyroid", "Follicular Cancer of the Thyroid", "follicular cancer of the thyroid", "Thyroid Gland Follicular Carcinoma", "Follicular Cancer of Thyroid Gland", "FTC - Follicular thyroid carcinoma", "follicular cancer of thyroid gland", "Follicular Thyroid Gland Carcinoma", "thyroid gland follicular carcinoma", "follicular thyroid gland carcinoma", "FTC - follicular thyroid carcinoma", "Follicular Carcinoma of the Thyroid", "follicular carcinoma of the thyroid", "THYROID CANCER, FOLLICULAR CARCINOMA", "carcinoma, follicular cell, malignant", "CARCINOMA, FOLLICULAR CELL, MALIGNANT", "follicular carcinoma of thyroid gland", "Follicular Carcinoma of Thyroid Gland", "follicular cancer of the thyroid gland", "Follicular Cancer of the Thyroid Gland", "thyroid malignant carcinoma follicular", "Follicular thyroid carcinoma (disorder)", "well-differentiated follicular carcinoma", "Well-differentiated Follicular Carcinoma", "Follicular carcinoma, pure follicle type", "follicular thyroid carcinoma (diagnosis)", "Well-Differentiated Follicular Carcinoma", "Follicular carcinoma, well differentiated", "Follicular Carcinoma of the Thyroid Gland", "follicular carcinoma of the thyroid gland", "follicular; carcinoma, well differentiated", "carcinoma; follicular, well differentiated", "Follicular carcinoma - well differentiated", "follicular adenocarcinoma of thyroid gland", "Well-differentiated Follicular Adenocarcinoma", "Follicular adenocarcinoma, pure follicle type", "well-differentiated follicular adenocarcinoma", "Well-Differentiated Follicular Adenocarcinoma", "follicular adenocarcinoma, well differentiated", "Follicular carcinoma, well differentiated type", "Follicular adenocarcinoma, well differentiated", "adenocarcinoma; follicular, well differentiated", "Follicular adenocarcinoma - well differentiated", "follicular; adenocarcinoma, well differentiated", "Follicular adenocarcinoma (morphologic abnormality)", "Follicular adenocarcinoma, well differentiated type", "follicular adenocarcinoma (morphologic abnormality)", "follicular adenocarcinoma of thyroid gland (diagnosis)", "follicular adenocarcinoma, well differentiated (morphologic abnormality)", "Follicular adenocarcinoma, well differentiated (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid gland follicular carcinoma", "shortest_name_length": 3}
{"curie": "MONDO:0019962", "names": ["thyroid lymphoma", "Thyroid Lymphoma", "Thyroid lymphoma", "Lymphoma of Thyroid", "lymphoma of thyroid", "thyroid gland lymphoma", "Thyroid Gland Lymphoma", "lymphoma of the thyroid", "Lymphoma of the Thyroid", "Lymphoma of Thyroid Gland", "lymphoma of thyroid gland", "lymphoma of the thyroid gland", "Lymphoma of the Thyroid Gland", "primary thyroid gland lymphoma", "Primary Thyroid Gland Lymphoma", "Malignant lymphoma of thyroid gland", "malignant lymphoma of thyroid gland", "Malignant lymphoma of thyroid gland (disorder)", "malignant lymphoma of thyroid gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid lymphoma", "shortest_name_length": 16}
{"curie": "UMLS:C1720008", "names": ["AIDS-Related Burkitt Lymphoma", "AIDS-Related Burkitt's Lymphoma", "AIDS Related Burkitt's Lymphoma", "AIDS-Associated Burkitt's Lymphoma", "Burkitt lymphoma associated with AIDS", "AIDS-related small noncleaved cell lymphoma", "AIDS Related Small Noncleaved Cell Lymphoma", "AIDS-Related Small Non-Cleaved Cell Lymphoma", "AIDS Related Small Non Cleaved Cell Lymphoma", "small noncleaved cell lymphoma, AIDS-related", "AIDS-Associated Small Noncleaved Cell Lymphoma", "AIDS-Associated Small Non Cleaved Cell Lymphoma", "Burkitt lymphoma associated with AIDS (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Burkitt lymphoma associated with AIDS", "shortest_name_length": 29}
{"curie": "UMLS:C2828192", "names": ["Stage IVA Gestational Trophoblastic Tumor", "Stage IVA Gestational Trophoblastic Tumor AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Gestational Trophoblastic Tumor AJCC v7", "shortest_name_length": 41}
{"curie": "MONDO:0005980", "names": ["Tick infestation", "Tick Infestation", "tick infestation", "Infestation, Tick", "Tick Infestations", "tick infestations", "Infestations, Tick", "Infestation by tick", "Infestation (by);tick(s)", "Ixodoidea infectious disease", "Ixodoidea disease or disorder", "Infestation by tick (disorder)", "Ixodoidea caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tick infestation", "shortest_name_length": 16}
{"curie": "MONDO:0016407", "names": ["Oligomeganephronia", "oligomeganephronia", "Oligomeganephronic hypoplasia", "Oligomeganephronic renal hypoplasia", "Oligomeganephronic hypoplasia of kidney", "Oligomeganephronic hypoplasia of kidney (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oligomeganephronia", "shortest_name_length": 18}
{"curie": "UMLS:C5555507", "names": ["Refractory Appendix Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Appendix Carcinoma", "shortest_name_length": 29}
{"curie": "UMLS:C1997614", "names": ["thromboembolism of vein", "Thromboembolism of vein", "Venous thromboembolic disease", "Thromboembolism of vein (disorder)", "thromboembolism of vein (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thromboembolism of vein", "shortest_name_length": 23}
{"curie": "UMLS:C5204072", "names": ["Locally Advanced Small Cell Carcinoma", "Locally Advanced Small Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Small Cell Neuroendocrine Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0006292", "names": ["dmm", "DMM", "MESOM", "Mesothelioma", "mesothelioma", "Cancer, mesothelioma", "mesothelioma, somatic", "Mesothelioma malignant", "malignant mesothelioma", "Malignant Mesothelioma", "Malignant mesothelioma", "Mesothelioma, malignant", "Malignant Mesotheliomas", "Mesothelioma, Malignant", "MESOTHELIOMA, MALIGNANT", "mesothelioma, malignant", "mesothelioma (diagnosis)", "Mesotheliomas, Malignant", "Mesothelioma malignant NOS", "Malignant Mesothelial Tumor", "malignant mesothelial tumor", "advanced mesothelial sarcoma", "mesothelial sarcoma, advanced", "malignant mesothelial neoplasm", "Diffuse malignant Mesothelioma", "Malignant Mesothelial Neoplasm", "diffuse malignant mesothelioma", "Malignant Diffuse Mesothelioma", "malignant tumor of Mesothelium", "malignant tumor of mesothelium", "Diffuse Malignant Mesothelioma", "Diffuse malignant mesothelioma", "Malignant Tumor of Mesothelium", "advanced malignant mesothelioma", "Mesothelioma malignant advanced", "Advanced Malignant Mesothelioma", "diffuse malignant mesotheliomas", "malignant neoplasm mesothelioma", "MESOTHELIOMA, DIFFUSE MALIGNANT", "malignant mesothelioma, advanced", "malignant mesothelioma (disease)", "Malignant Neoplasm of Mesothelium", "malignant neoplasm of mesothelium", "mesothelioma, malignant, advanced", "malignant tumor of the mesothelium", "Malignant Tumor of the Mesothelium", "[OBSOLETE] Mesothelioma, Malignant", "diffuse malignant mesothelioma (DMM)", "malignant neoplasm of the mesothelium", "Malignant Neoplasm of the Mesothelium", "Asbestos-Related Malignant Mesothelioma", "asbestos-related malignant mesothelioma", "Mesothelioma (malignant, clinical disorder)", "Mesothelioma, malignant (morphologic abnormality)", "Mesothelioma (malignant, clinical disorder) (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant mesothelioma", "shortest_name_length": 3}
{"curie": "UMLS:C0521707", "names": ["Cataracts", "Bilateral cataract", "Cataract, bilateral", "Bilateral Cataracts", "bilateral cataracts", "Bilateral cataracts", "Cataract bilateral NOS", "Bilateral cataracts (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bilateral cataracts (disorder)", "shortest_name_length": 9}
{"curie": "MONDO:0012620", "names": ["HPC10", "prostate cancer, hereditary, 10", "PROSTATE CANCER, HEREDITARY, 10", "Prostate Cancer, Hereditary, 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate cancer, hereditary, 10", "shortest_name_length": 5}
{"curie": "MONDO:0009699", "names": ["AMRF", "EPM4", "MYOCLONUS-NEPHROPATHY SYNDROME", "Myoclonus Nephropathy Syndrome", "myoclonus-nephropathy syndrome", "Myoclonus nephropathy syndrome", "Myoclonus-nephropathy syndrome", "Myoclonus-Nephropathy Syndrome", "Myoclonus-Nephropathy Syndromes", "progressive myoclonus epilepsy 4", "Syndromes, Myoclonus-Nephropathy", "progressive myoclonic epilepsy type 4", "Progressive myoclonus epilepsy type 4", "AMRF - action myoclonus renal failure", "Progressive myoclonic epilepsy type 4", "Action myoclonus renal failure syndrome", "ACTION MYOCLONUS-RENAL FAILURE SYNDROME", "Action Myoclonus-Renal Failure Syndrome", "action myoclonus-renal failure syndrome", "Action myoclonus-renal failure syndrome", "Action Myoclonus Renal Failure Syndrome", "Action myoclonus renal failure syndrome (disorder)", "epilepsy, progressive myoclonic 4, with or without renal failure", "epilepsy, progressive myoclonic, 4, with or without renal failure", "EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "action myoclonus-renal failure syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0014980", "names": ["CRDHL", "cone-rod dystrophy and hearing loss", "cone-rod dystrophy and hearing loss; CRDHL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cone-rod dystrophy and hearing loss", "shortest_name_length": 5}
{"curie": "UMLS:C5670006", "names": ["Psychiatric Toxicity", "Toxicity due to Psychiatric Drugs"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Toxicity due to Psychiatric Drugs", "shortest_name_length": 20}
{"curie": "UMLS:C3897540", "names": ["Stage IB Esophageal Cancer", "Stage IB Esophageal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Esophageal Cancer AJCC v7", "shortest_name_length": 26}
{"curie": "UMLS:C0919570", "names": ["Mental status changes postoperative"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mental status changes postoperative", "shortest_name_length": 35}
{"curie": "MONDO:0001560", "names": ["IHPS", "Pyloric stenosis", "Pylorus stenosis", "Infantile pyloric stenosis", "infantile pyloric stenosis", "Infantile Pyloric Stenosis", "congenital pyloric stenosis", "PYLORIC STENOSIS, INFANTILE", "pyloric stenosis, infantile", "Congenital Pyloric Stenosis", "pyloric hypertrophic stenosis", "hypertrophic pyloric stenosis", "Hypertrophic Pyloric Stenosis", "Hypertrophic pyloric stenosis", "Pyloric Stenosis, Hypertrophic", "infantile; pyloric obstruction", "Stenosis, Hypertrophic Pyloric", "Pyloric stenosis, hypertrophic", "hypertrophy; pylorus, infantile", "pylorus; hypertrophy, infantile", "Infantile Stricture of the Pylorus", "infantile stricture of the pylorus", "congenital stricture of the pylorus", "Congenital Stricture of the Pylorus", "Infantile Hypertrophy of the Pylorus", "infantile Hypertrophy of the pylorus", "congenital Hypertrophy of the pylorus", "infantile constriction of the pylorus", "Infantile Constriction of the Pylorus", "Congenital Hypertrophy of the Pylorus", "congenital constriction of the pylorus", "Congenital Constriction of the Pylorus", "infantile hypertrophic pyloric stenosis", "Infantile hypertrophic pyloric stenosis", "Congenital hypertrophic pyloric stenosis", "STENOSIS PYLORIC HYPERTROPHIC CONGENITAL", "congenital hypertrophic pyloric stenosis", "PYLORIC STENOSIS, INFANTILE HYPERTROPHIC", "Stenosis pyloric hypertrophic congenital", "PYLORIC STENOSIS, CONGENITAL HYPERTROPHIC", "Congenital or infantile stenosis of pylorus", "Congenital or infantile stricture of pylorus", "congenital or infantile stricture of pylorus", "Congenital or infantile hypertrophy of pylorus", "Congenital or infantile constriction of pylorus", "Congenital hypertrophic pyloric stenosis (disorder)", "congenital hypertrophic pyloric stenosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophic pyloric stenosis", "shortest_name_length": 4}
{"curie": "MONDO:0024326", "names": ["pleura adenomatoid tumor", "Pleural Adenomatoid Tumor", "pleural adenomatoid tumor", "Pleural Benign Mesothelioma", "pleural benign mesothelioma", "Pleural Mesothelioma, Benign", "pleural mesothelioma, benign", "Benign Mesothelioma of Pleura", "benign mesothelioma of pleura", "Benign Mesothelioma of the Pleura", "benign mesothelioma of the pleura"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pleural adenomatoid tumor", "shortest_name_length": 24}
{"curie": "MONDO:0016985", "names": ["ITO", "IPA", "HMI", "nevi of Ito", "Ito's nevus", "Ito's Nevus", "Nevus of Ito", "Ito syndrome", "Ito Syndrome", "nevus of ito", "ito syndrome", "nevus of Ito", "Ito's naevus", "syndrome ito", "IP1, FORMERLY", "Naevus of Ito", "Syndrome, Ito", "Ito's syndrome", "ITO HYPOMELANOSIS", "hypomelanosis ito", "ito hypomelanosis", "Ito hypomelanosis", "Hypomelanosis of Ito", "hypomelanosis of ito", "hypomelanosis of Ito", "HYPOMELANOSIS OF ITO", "bloch-siemens syndrome", "Nevus of Ito (disorder)", "HMI - Hypomelanosis of Ito", "hypomelanosis of Ito (HI, HMI)", "Incontinentia pigmenti achromians", "INCONTINENTIA PIGMENTI ACHROMIANS", "achromians incontinentia pigmenti", "Incontinentia Pigmenti Achromians", "Nevus fusoceruleus acromiodeltoideus", "Naevus fusoceruleus acromiodeltoideus", "nevus fuscocaeruleus acromiodeltoideus", "Nevus fuscocaeruleus acromiodeltoideus", "Incontinentia pigmenti achromians (IPA)", "INCONTINENTIA PIGMENTI, TYPE I, FORMERLY", "Incontinentia pigmenti achromicans of Ito", "Incontinentia pigmenti achromians syndrome", "Incontinentia pigmenti achromians syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nevus of Ito", "shortest_name_length": 3}
{"curie": "MONDO:0011710", "names": ["SLI1", "SPECIFIC LANGUAGE IMPAIRMENT 1", "specific language impairment 1", "specific language impairment QTL, 1", "specific language impairment quantitative trait locus on chromosome 16", "SPECIFIC LANGUAGE IMPAIRMENT QUANTITATIVE TRAIT LOCUS ON CHROMOSOME 16"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "specific language impairment 1", "shortest_name_length": 4}
{"curie": "MONDO:0000248", "names": ["DSS", "Severe dengue", "Severe Dengue", "Dengue, Severe", "Severe Dengues", "Dengues, Severe", "dengue hemorrhagic", "HEMORRHAGIC DENGUE", "Hemorrhagic Dengue", "dengue; hemorrhagic", "Hemorrhagic Dengues", "hemorrhagic; dengue", "dengue shock syndrome", "Dengue Shock Syndrome", "Dengue shock syndrome", "Thai Hemorrhagic Fever", "Fever, Thai Hemorrhagic", "Dengue hemorrhagic fever", "dengue hemorrhagic fever", "hemorrhagic dengue fever", "DENGUE HEMORRHAGIC FEVER", "dengue fever hemorrhagic", "Dengue Hemorrhagic Fever", "Hemorrhagic Fever, Dengue", "dengue fever haemorrhagic", "dengue haemorrhagic fever", "haemorrhagic dengue fever", "dengue; hemorrhagic fever", "hemorrhagic fever; dengue", "Dengue haemorrhagic fever", "bangkok hemorrhagic; fever", "hemorrhagic fever; Bangkok", "fever; bangkok hemorrhagic", "Bangkok; hemorrhagic fever", "Singapore Hemorrhagic Fever", "Thailand; hemorrhagic fever", "hemorrhagic fever; Thailand", "Singapore; hemorrhagic fever", "Fever, Singapore Hemorrhagic", "hemorrhagic fever; Singapore", "Philippine Hemorrhagic Fever", "hemorrhagic fever; Philippine", "Fever, Philippine Hemorrhagic", "Philippine; hemorrhagic fever", "DHF - Dengue hemorrhagic fever", "DHF - Dengue haemorrhagic fever", "Dengue shock syndrome (disorder)", "virus; dengue, hemorrhagic fever", "DOUBLE DENGUE HEMORRHAGIC DISEASE", "fever; dengue (virus), hemorrhagic", "dengue (virus); fever, hemorrhagic", "Dengue hemorrhagic fever (disorder)", "Dengue hemorrhagic fever (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dengue shock syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0011202", "names": ["RHYNS", "RHYNS syndrome", "RHYNS SYNDROME", "retinitis pigmentosa syndrome", "RETINITIS PIGMENTOSA SYNDROME", "Retinitis pigmentosa syndrome", "Retinitis pigmentosa-hypopituitarism-nephronophthisis-skeletal dysplasia syndrome", "retinitis pigmentosa-hypopituitarism-nephronophthisis-skeletal dysplasia syndrome", "retinitis pigmentosa, hypopituitarism, nephronophthisis, and mild skeletal dysplasia", "RETINITIS PIGMENTOSA, HYPOPITUITARISM, NEPHRONOPHTHISIS, AND MILD SKELETAL DYSPLASIA", "Retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia syndrome", "Retinitis pigmentosa, HYpopituitarism, Nephronophthisis, and mild Skeletal dysplasia", "RHYNS (retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia) syndrome", "Retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "RHYNS syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0100095", "names": ["CONDSIAS", "stress-induced childhood-onset neurodegeneration with variable ataxia and seizures", "neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures", "NEURODEGENERATION, CHILDHOOD-ONSET, STRESS-INDUCED, WITH VARIABLE ATAXIA AND SEIZURES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures", "shortest_name_length": 8}
{"curie": "MONDO:0010978", "names": ["Portal vein cavernous transformation", "Cavernous transformation of portal vein", "portal vein, cavernous transformation of", "Portal Vein, Cavernous Transformation Of", "PORTAL VEIN, CAVERNOUS TRANSFORMATION OF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "portal vein, cavernous transformation of", "shortest_name_length": 36}
{"curie": "MONDO:0013835", "names": ["MDDGA7", "ISPD muscular dystrophy-dystroglycanopathy, type A", "congenital muscular dystrophy-dystroglycanopathy A7", "Walker-Warburg syndrome or muscle-eye-brain disease ISPD-related", "WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, ISPD-RELATED", "Walker-Warburg syndrome or muscle-eye-brain disease, ISPD-related", "muscular dystrophy-dystroglycanopathy, type A caused by mutation in ISPD", "congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A7", "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7", "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7", "shortest_name_length": 6}
{"curie": "UMLS:C0861816", "names": ["Metastatic Malignant Small Intestinal Neoplasm", "Malignant small intestinal neoplasm metastatic NOS", "Malignant neoplasm of small intestine, unspecified metastatic", "Malignant neoplasm of small intestine, incl duodenum metastatic", "Malignant neoplasm of small intestine, including duodenum metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant neoplasm of small intestine, incl duodenum metastatic", "shortest_name_length": 46}
{"curie": "MONDO:0008936", "names": ["cerebellar ataxia and neurosensory deafness", "CEREBELLAR ATAXIA AND NEUROSENSORY DEAFNESS", "Cerebellar Ataxia and Neurosensory Deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellar ataxia and neurosensory deafness", "shortest_name_length": 43}
{"curie": "UMLS:C4521813", "names": ["Stage IIIB Appendix Cancer", "Stage IIIB Appendix Carcinoma AJCC v8", "Stage IIIB Appendiceal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Appendix Carcinoma AJCC v8", "shortest_name_length": 26}
{"curie": "UMLS:C0281838", "names": ["esophagus polyp", "polyp esophagus", "Esophageal Polyp", "Esophageal polyp", "esophageal polyp", "esophagus polyps", "oesophagus polyp", "esophageal polyps", "Oesophageal polyp", "polyp of esophagus", "Polyp of esophagus", "Polyp of oesophagus", "esophageal disorders polyp", "esophageal polyp (diagnosis)", "Polyp of esophagus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Polyp of esophagus", "shortest_name_length": 15}
{"curie": "UMLS:C1257798", "names": ["Choledochal Cyst, Type IV", "Multiple Choledochal Cyst", "Cyst, Multiple Choledochal", "Choledochal Cyst, Multiple", "Multiple Choledochal Cysts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Choledochal Cyst, Type IV", "shortest_name_length": 25}
{"curie": "MONDO:0016670", "names": ["HbSD disease", "HbS-HbD disease", "Hemoglobin SD Disease", "Hemoglobin SD disease", "Haemoglobin SD disease", "Hemoglobin S-D disease", "Haemoglobin S-D disease", "Sickle cell hemoglobin D", "Sickle cell haemoglobin D", "Hemoglobin S/D Punjab disease", "Haemoglobin S/D Punjab disease", "Sickle Cell-Hemoglobin D Disease", "sickle cell-hemoglobin D disease", "Sickle cell-hemoglobin D disease", "Sickle cell-haemoglobin D disease", "sickle cell - hemoglobin D disease", "anemia hemolytic sickle Hb-D disease", "sickle cell-hemoglobin d disease syndrome", "Sickle cell-hemoglobin D disease syndrome", "Double heterozygous for Hb S + Hb D Punjab", "Sickle cell-hemoglobin D disease (disorder)", "Sickle cell anemia with hemoglobin D disease", "sickle cell-hemoglobin D disease (diagnosis)", "Sickle cell anaemia with haemoglobin D disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sickle cell-hemoglobin d disease syndrome", "shortest_name_length": 12}
{"curie": "UMLS:C0684550", "names": ["spine metastasis", "spine metastases", "metastasis spine", "spinal metastases", "Spinal metastases", "Spinal secondaries", "Metastasis to Spine", "Metastases to Spine", "metastasis to spine", "Metastasis to spine", "Metastases to spine", "vertebral metastasis", "Metastases to the Spine", "Metastasis to the Spine", "Secondary tumor of spine", "Secondary tumour of spine", "Secondary cancer of spine", "Metastatic Tumor to the Spine", "Metastasis to vertebral column", "Metastatic Cancer to the Spine", "CA - Secondary cancer of spine", "Metastatic Neoplasm to the Spine", "vertebral metastasis (diagnosis)", "Secondary malignant neoplasm of spine", "Metastatic malignant neoplasm to spine", "Metastatic Tumor to the Vertebral Column", "Metastatic Cancer to the Vertebral Column", "Metastatic Malignant Neoplasm in the Spine", "Secondary malignant neoplasm of spine, NOS", "Metastatic Malignant Neoplasm to the Spine", "Metastatic malignant neoplasm to spine, NOS", "Metastatic Neoplasm to the Vertebral Column", "secondary malignant neoplasm of vertebral column", "Secondary malignant neoplasm of vertebral column", "Metastatic malignant neoplasm of vertebral column", "Metastatic malignant neoplasm to vertebral column", "Secondary malignant neoplasm of vertebral column, NOS", "bone neoplasm, malignant - vertebral column secondary", "Metastatic malignant neoplasm to vertebral column, NOS", "Metastatic malignant neoplasm to vertebral column (disorder)", "secondary malignant neoplasm of vertebral column (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to vertebral column", "shortest_name_length": 16}
{"curie": "UMLS:C0346351", "names": ["Orbit Capillary Angioma", "Capillary Angioma of Orbit", "Orbit Capillary Hemangioma", "capillary orbital hemangioma", "orbital hemangioma capillary", "Capillary hemangioma of orbit", "Capillary Hemangioma of Orbit", "Capillary haemangioma of orbit", "Capillary Angioma of the Orbit", "Capillary Hemangioma of the Orbit", "capillary orbital hemangioma (diagnosis)", "Capillary hemangioma of orbit (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Capillary hemangioma of orbit", "shortest_name_length": 23}
{"curie": "UMLS:C4682566", "names": ["Uterine Corpus Endometrial Stromal Sarcoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Corpus Endometrial Stromal Sarcoma by AJCC v8 Stage", "shortest_name_length": 59}
{"curie": "MONDO:0006220", "names": ["gallbladder squamous cell cancer", "Epidermoid Gallbladder Carcinoma", "Epidermoid gallbladder carcinoma", "Gallbladder Squamous Cell Cancer", "epidermoid gallbladder carcinoma", "Epidermoid Carcinoma of Gallbladder", "epidermoid carcinoma of gallbladder", "squamous cell gallbladder carcinoma", "Gallbladder squamous cell carcinoma", "Squamous Cell Gallbladder Carcinoma", "gallbladder squamous cell carcinoma", "Gallbladder Squamous Cell Carcinoma", "gall bladder squamous cell carcinoma", "squamous cell carcinoma of gallbladder", "Squamous Cell Carcinoma of Gallbladder", "epidermoid carcinoma of the gallbladder", "Epidermoid Carcinoma of the Gallbladder", "gallbladder cancer, epidermoid carcinoma", "Squamous Cell Carcinoma of the Gallbladder", "squamous cell carcinoma of the gallbladder", "gallbladder, squamous cell carcinoma of the", "gallbladder cancer, squamous cell carcinoma", "squamous cell carcinoma of gallbladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gallbladder squamous cell carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0014931", "names": ["ALYUS", "ALAZAMI-YUAN SYNDROME", "Alazami-Yuan syndrome", "Alazami-Yuan syndrome; ALYUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alazami-Yuan syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0008867", "names": ["Biliary Atresia", "Atresia;biliary", "Atresia biliary", "atresia biliary", "Biliary atresia", "ATRESIA BILIARY", "BILIARY ATRESIA", "biliary atresia", "Atresia, Biliary", "atresia; bile duct", "bile duct; atresia", "atresia bile ducts", "Atresia of bile duct", "BA - Biliary atresia", "Biliary duct atresia", "atresia of bile duct", "Atresia of bile ducts", "bile duct; impervious", "atresia of bile ducts", "impervious; bile duct", "primary biliary atresia", "PRIMARY BILIARY ATRESIA", "isolated biliary atresia", "Congenital Biliary Atresia", "Congenital biliary atresia", "congenital biliary atresia", "Biliary atresia, congenital", "biliary atresia, congenital", "biliary atresia (diagnosis)", "Congenital bile duct atresia", "non-syndromic biliary atresia", "isolated atresia of bile ducts", "atresia of bile ducts (diagnosis)", "Congenital biliary atresia (disorder)", "congenital biliary atresia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "biliary atresia", "shortest_name_length": 15}
{"curie": "MONDO:0013763", "names": ["JBTS15", "JOUBERT SYNDROME 15", "Joubert syndrome 15", "CEP41 Joubert syndrome", "Joubert syndrome type 15", "Joubert syndrome 9/15, digenic", "Joubert syndrome 12/15, digenic", "Joubert syndrome caused by mutation in CEP41"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome 15", "shortest_name_length": 6}
{"curie": "UMLS:C1970106", "names": ["Bpes, Type I, Autosomal Recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bpes, Type I, Autosomal Recessive", "shortest_name_length": 33}
{"curie": "MONDO:0024552", "names": ["MLS", "MCOPS7", "LSDMCA1", "MLS syndrome", "Midas syndrome", "MIDAS syndrome", "MIDAS SYNDROME", "Midas Syndrome", "syndromic microphthalmia 7", "Syndromic Microphthalmia-7", "MICROPHTHALMIA, SYNDROMIC 7", "microphthalmia, syndromic 7", "Microphthalmia, syndromic 7", "Syndromic microphthalmia type 7", "syndromic microphthalmia type 7", "MICROPHTHALMIA WITH LINEAR SKIN DEFECTS", "microphthalmia with linear skin defects", "Microphthalmia with linear skin defects", "microphthalmia with linear skin defects (MLS)", "Microphthalmia with linear skin defect syndrome", "Microphthalmia with Linear Skin Defects Syndrome", "Microphthalmia, dermal aplasia, and sclerocornea", "Microphthalmia with linear skin defects syndrome", "MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA", "microphthalmia, dermal aplasia, and sclerocornea", "Microphthalmia with Linear Skin Lesions Syndrome", "Microphthalmia-dermal aplasia-sclerocornea syndrome", "microphthalmia-dermal aplasia-sclerocornea syndrome", "HCCS microphthalmia with linear skin defects syndrome", "linear skin defects with multiple congenital anomalies 1", "Linear skin defects with multiple congenital anomalies 1", "LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 1", "Microphthalmia with linear skin defect syndrome (disorder)", "microphthalmia-dermal aplasia-sclerocornea (MIDAS) syndrome", "MIDAS syndrome (microphthalmia, dermal aplasia, sclerocornea) syndrome", "microphthalmia with linear skin defects syndrome caused by mutation in HCCS", "linear skin defects with multiple congenital anomalies 1, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "linear skin defects with multiple congenital anomalies 1", "shortest_name_length": 3}
{"curie": "UMLS:C4727006", "names": ["Unresectable Bone Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Bone Sarcoma", "shortest_name_length": 25}
{"curie": "MONDO:0008247", "names": ["Robin sequence and oligodactyly", "ROBIN SEQUENCE AND OLIGODACTYLY", "robin sequence-oligodactyly syndrome", "PIERRE ROBIN SYNDROME AND OLIGODACTYLY", "Pierre Robin syndrome and oligodactyly", "Pierre Robin sequence-oligodactyly syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "robin sequence-oligodactyly syndrome", "shortest_name_length": 31}
{"curie": "MONDO:0010137", "names": ["TDH5", "GDTH V", "Thyroid Dyshormonogenesis 5", "thyroid dyshormonogenesis 5", "THYROID DYSHORMONOGENESIS 5", "Thyroglobulin synthesis defect", "thyroid dyshormonogenesis type 5", "Thyroglobulin synthesis defect (disorder)", "DUOXA2 familial thyroid dyshormonogenesis", "Genetic defect in thyroid hormonogenesis V", "genetic defect in thyroid hormonogenesis 5", "thyroid hormonogenesis, genetic defect in, 5", "THYROID HORMONOGENESIS, GENETIC DEFECT IN, 5", "Thyroid Hormonogenesis, Genetic Defect in, 5", "Hypothyroidism due to thyroglobulin synthesis defect", "hypothyroidism, congenital, due to dyshormonogenesis, 5", "Hypothyroidism due to thyroglobulin biosynthetic defect", "Hypothyroidism, Congenital, due to Dyshormonogenesis, 5", "HYPOTHYROIDISM, CONGENITAL, DUE TO DYSHORMONOGENESIS, 5", "familial thyroid dyshormonogenesis caused by mutation in DUOXA2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid dyshormonogenesis 5", "shortest_name_length": 4}
{"curie": "UMLS:C0751238", "names": ["Hypothalamic Cancer", "Hypothalamic Cancers", "Cancer, Hypothalamic", "Cancers, Hypothalamic", "Malignant Hypothalamic Neoplasm", "Neoplasm, Malignant Hypothalamic", "Hypothalamic Neoplasm, Malignant", "Malignant Hypothalamic Neoplasms", "Neoplasms, Malignant Hypothalamic", "Hypothalamic Neoplasms, Malignant", "Neoplasms, Hypothalamic, Malignant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypothalamic Cancer", "shortest_name_length": 19}
{"curie": "UMLS:C0796293", "names": ["Stage II Immunoblastic Lymphoma", "Stage II Adult Non-Contiguous Immunoblastic Lymphoma", "stage II adult non-contiguous immunoblastic lymphoma", "NonContiguous Adult Immunoblastic Large Cell Lymphoma Stage II", "noncontiguous stage II adult immunoblastic large cell lymphoma", "stage II noncontiguous adult immunoblastic large cell lymphoma", "Stage II NonContiguous Adult Immunoblastic Large Cell Lymphoma", "noncontiguous adult immunoblastic large cell lymphoma stage II", "Ann Arbor Stage II Adult Non-Contiguous Immunoblastic Lymphoma", "non-contiguous adult immunoblastic large cell lymphoma stage II", "stage II non-contiguous adult immunoblastic large cell lymphoma", "Stage II Non-Contiguous Adult Immunoblastic Large Cell Lymphoma", "Non-Contiguous Adult Immunoblastic Large Cell Lymphoma Stage II", "Non-Contiguous Stage II Adult Immunoblastic Large Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage II Adult Non-Contiguous Immunoblastic Lymphoma", "shortest_name_length": 31}
{"curie": "MONDO:0022776", "names": ["cleft lip and/or palate with mucous cysts of lower"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleft lip and/or palate with mucous cysts of lower", "shortest_name_length": 50}
{"curie": "MONDO:0019908", "names": ["R15", "Ring 15", "(15)r syndrome", "r(15) syndrome", "chromosome 15 ring", "Ring chromosome 15", "ring chromosome 15", "Chromosome 15 ring", "Ring 15, Chromosome", "Ring chromosome type 15", "Ring chromosome 15 syndrome", "chromosome 15 ring syndrome", "ring chromosome 15 syndrome", "Ring 15, Chromosome (mosaic pattern)", "Ring chromosome 15 syndrome (disorder)", "Ring chromosome 15 syndrome (diagnosis)", "anomaly of chromosome pair ring chromosome 15 syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ring chromosome 15", "shortest_name_length": 3}
{"curie": "UMLS:C1141885", "names": ["encapsulating peritonitis sclerosing", "Sclerosing encapsulating peritonitis", "sclerosing encapsulating peritonitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sclerosing encapsulating peritonitis", "shortest_name_length": 36}
{"curie": "MONDO:0001458", "names": ["Ulnar nerve lesion", "ulnar nerve lesion", "lesion of ulnar nerve", "Lesion of ulnar nerve", "Ulnar nerve lesion NOS", "Lesion of ulnar nerve, NOS", "Lesion of ulnar nerve (disorder)", "ulnar nerve peripheral nerve lesion", "peripheral nerve lesion of ulnar nerve", "Lesion of ulnar nerve, unspecified upper limb"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ulnar nerve lesion", "shortest_name_length": 18}
{"curie": "UMLS:C4687708", "names": ["Refractory Ependymoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Ependymoma", "shortest_name_length": 21}
{"curie": "MONDO:0044688", "names": ["ion", "isolated optic neuritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated optic neuritis", "shortest_name_length": 3}
{"curie": "UMLS:C4331327", "names": ["Stage III Lip and Oral Cavity Cancer", "Stage III Lip and Oral Cavity Cancer AJCC v8", "Stage III Lip and Oral Cavity Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Lip and Oral Cavity Cancer AJCC v8", "shortest_name_length": 36}
{"curie": "MONDO:0021660", "names": ["Deep dermatophytosis", "deep dermatophytosis", "deep; dermatophytosis", "dermatophytosis; deep", "Dermatophytic mycetoma", "Dermatophytic granuloma", "Granuloma trichophyticum", "Dermatophytosis profunda", "granuloma; trichophyticum", "trichophyticum; granuloma", "Deep seated dermatophytosis", "deep seated dermatophytosis", "Deep Seated Dermatophytosis", "Deep seated dermatophytosis (disorder)", "deep seated dermatophytosis (diagnosis)", "Disseminated granulomatous dermatophytosis", "disseminated granulomatous dermatophytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deep seated dermatophytosis", "shortest_name_length": 20}
{"curie": "UMLS:C0454608", "names": ["Oral Apraxia", "Oral apraxia", "oral apraxia", "Oral Apraxias", "Apraxia, Oral", "Oral Dyspraxia", "oral dyspraxia", "Oral dyspraxia", "Apraxias, Oral", "Dyspraxia, Oral", "Oral Dyspraxias", "Dyspraxias, Oral", "Oral apraxia (disorder)", "Oral dyspraxia (disorder)", "Oral dyspraxia (diagnosis)", "developmental disorder speech and language dyspraxias oral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Apraxia, Oral", "shortest_name_length": 12}
{"curie": "UMLS:C1704613", "names": ["CASTLE", "Intrathyroid Thymic Carcinoma", "CD5-Positive Thyroid Carcinoma", "Intrathyroidal Carcinoma Showing Thymus-Like Elements", "Thyroid Gland Carcinoma Showing Thymus-Like Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Carcinoma Showing Thymus-Like Differentiation", "shortest_name_length": 6}
{"curie": "MONDO:0012588", "names": ["CLN7", "CLN7 disease", "CLN7 disease, late infantile", "neuronal ceroid lipofuscinosis 7", "ceroid lipofuscinosis, neuronal, 7", "CEROID LIPOFUSCINOSIS, NEURONAL, 7", "Ceroid Lipofuscinosis, Neuronal, 7", "MFSD8 neuronal ceroid lipofuscinosis", "neuronal ceroid lipofuscinosis type 7", "ceroid lipofuscinosis, neuronal, type 7", "neuronal ceroid lipofuscinosis caused by mutation in MFSD8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuronal ceroid lipofuscinosis 7", "shortest_name_length": 4}
{"curie": "MONDO:0019222", "names": ["Sulfuraminoacidemia", "Sulphuraminoacidaemia", "Sulfuraminoacidemia, NOS", "Disorder of transsulfuration", "Disorder of transsulphuration", "Disorder of transsulfuration, NOS", "metabolic disorder; sulfur-bearing amino-acid", "sulfur-bearing amino-acid; metabolic disorder", "metabolic disorder; amino-acid, sulfur-bearing", "amino-acid; metabolic disorder, sulfur-bearing", "Disorder of sulfur-bearing amino acid metabolism", "Disorders of sulfur-bearing amino-acid metabolism", "sulfur-bearing amino-acid metabolism disturbances", "Disorder of sulphur-bearing amino acid metabolism", "DISORDERS OF SULPHUR-BEARING AMINO ACID METABOLISM", "inborn sulfur amino acid metabolic process disorder", "inborn error of sulfur amino acid metabolic process", "Disturbances of sulphur-bearing amino-acid metabolism", "Disorder of sulphur-bearing amino acid metabolism, NOS", "rare inborn error of sulfur amino acid metabolic process", "Disorder of sulfur-bearing amino acid metabolism (disorder)", "disorder of methionine cycle and sulfur amino acid metabolism", "sulfur-bearing amino-acid metabolism disturbances (diagnosis)", "Disorders of sulfur-bearing amino-acid metabolism, unspecified", "inborn disorder of methionine cycle and sulfur amino acid metabolism", "cytosolic methyl group transfer or sulfur amino acid metabolism disorder", "Disorder of sulfur-bearing amino acid including those due to folate and B12 disturbance", "Disorder of sulphur-bearing amino acid including those due to folate and B12 disturbance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of methionine cycle and sulfur amino acid metabolism", "shortest_name_length": 19}
{"curie": "MONDO:0021041", "names": ["Pleural fibroma", "Pleural Fibroma", "pleural fibroma", "Fibroma of Pleura", "fibroma of pleura", "Fibrous Mesothelioma", "fibroma of the pleura", "Fibroma of the Pleura", "Fibrous Mesotheliomas", "Mesothelioma, Fibrous", "Localized Mesothelioma", "Mesotheliomas, Fibrous", "Submesothelial Fibroma", "Mesothelioma, Localized", "Submesothelial Fibromas", "Fibroma, Submesothelial", "Localized Mesotheliomas", "Fibromas, Submesothelial", "Mesotheliomas, Localized", "Pleural fibroma (disorder)", "Benign Fibrous Mesothelioma", "benign fibrous mesothelioma", "Benign fibrous mesothelioma", "fibrous mesothelioma, benign", "Benign Fibrous Mesotheliomas", "Mesothelioma, Benign Fibrous", "Fibrous mesothelioma, benign", "Fibrous Mesothelioma, Benign", "Mesotheliomas, Benign Fibrous", "Solitary Fibrous Mesothelioma", "pleura solitary fibrous tumor", "Fibrous Mesotheliomas, Benign", "Mesothelioma, Solitary Fibrous", "pleural solitary fibrous tumor", "pleural Submesothelial fibroma", "Pleural Solitary Fibrous Tumor", "Pleural Submesothelial Fibroma", "Solitary Fibrous Mesotheliomas", "Localized Fibrous Mesothelioma", "Fibrous Mesothelioma, Solitary", "Mesothelioma, Localized Fibrous", "Localized Fibrous Mesotheliomas", "Solitary Fibrous Tumor, Pleural", "Fibrous Mesotheliomas, Solitary", "Mesotheliomas, Solitary Fibrous", "Fibrous Mesothelioma, Localized", "Solitary fibrous tumor of pleura", "Fibrous Mesotheliomas, Localized", "Solitary Fibrous Tumor of Pleura", "solitary fibrous tumor of pleura", "Mesotheliomas, Localized Fibrous", "Solitary fibrous tumour of pleura", "Localized fibrous tumor of pleura", "Localised fibrous tumour of pleura", "solitary fibrous tumor of the pleura", "Solitary Fibrous Tumor of the Pleura", "pleural cavity solitary fibrous tumor", "localized benign fibrous Mesothelioma", "localized fibrous mesothelioma of pleura", "Localized Fibrous Mesothelioma of Pleura", "Localized Fibrous Mesothelioma of the Pleura", "localized fibrous mesothelioma of the pleura", "Fibrous mesothelioma, benign (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pleural solitary fibrous tumor", "shortest_name_length": 15}
{"curie": "MONDO:0011537", "names": ["macrocephaly-autism syndrome", "MACROCEPHALY/AUTISM SYNDROME", "Macrocephaly Autism Syndrome", "macrocephaly/autism syndrome", "macrocephaly-intellectual disability-autism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macrocephaly-autism syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0003859", "names": ["bilateral optic nerve meningioma", "Bilateral Optic Nerve Meningioma", "Bilateral Meningioma of Optic Nerve", "bilateral meningioma of optic nerve", "Bilateral Meningioma of the Optic Nerve", "bilateral meningioma of the optic nerve", "Bilateral meningioma of the optic nerve"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bilateral meningioma of optic nerve", "shortest_name_length": 32}
{"curie": "MONDO:0019053", "names": ["peroxisomal disease", "Peroxisomal Disorder", "peroxisomal disorder", "Peroxisomal Disorders", "peroxisomal disorders", "Peroxisomal disorders", "peroxisomal function disorder", "Peroxisomal Function Disorder", "peroxisomal biogenesis disorder", "Disorder of peroxisomal function", "disorder of peroxisomal function", "peroxisomal disorder (diagnosis)", "Disorder of Peroxisomal Function", "Peroxisomal disorder, unspecified", "peroxisomal biogenesis disorder (diagnosis)", "Disorder of peroxisomal function (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisomal disease", "shortest_name_length": 19}
{"curie": "MONDO:0014496", "names": ["MC3DN9", "UQCC3 mitochondrial complex III deficiency", "mitochondrial Complex 3 deficiency, nuclear type 9", "mitochondrial complex III deficiency nuclear type 9", "mitochondrial complex III deficiency, nuclear type 9", "MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 9", "mitochondrial complex III deficiency caused by mutation in UQCC3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex III deficiency nuclear type 9", "shortest_name_length": 6}
{"curie": "UMLS:C5205581", "names": ["Metastatic Rectal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Rectal Adenocarcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C3273226", "names": ["Giant Cell Angioblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Giant Cell Angioblastoma", "shortest_name_length": 24}
{"curie": "UMLS:C0334251", "names": ["Epidermoid carcinoma in-situ with questionable stromal invasion", "Epidermoid carcinoma in situ with questionable stromal invasion", "carcinoma in situ squamous cell with questionable stromal invasion", "Squamous cell carcinoma in situ with questionable stromal invasion", "squamous cell carcinoma in situ with questionable stromal invasion", "Squamous Cell Carcinoma In Situ with Questionable Stromal Invasion", "Squamous cell carcinoma in-situ with questionable stromal invasion", "squamous cell carcinoma in situ with questionable stromal invasion (diagnosis)", "Squamous cell carcinoma in situ with questionable stromal invasion (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Squamous cell carcinoma in situ with questionable stromal invasion", "shortest_name_length": 63}
{"curie": "MONDO:0032615", "names": ["MC1DN9", "nuclear type mitochondrial complex I deficiency 9", "mitochondrial complex 1 deficiency, nuclear type 9", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 9", "shortest_name_length": 6}
{"curie": "MONDO:0019759", "names": ["epispadia", "Epispadia", "EPISPADIAS", "Anaspadias", "epispadias", "Epispadias", "epispadias (disease)", "Epispadias (disorder)", "URETHRAL MEATUS, DORSAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epispadias", "shortest_name_length": 9}
{"curie": "MONDO:0017595", "names": ["Aggressive B-cell NHL", "aggressive B-cell NHL", "Aggressive B-Cell Non-Hodgkin Lymphoma", "aggressive B-cell non-Hodgkin lymphoma", "Aggressive B-cell non-Hodgkin lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aggressive B-cell non-Hodgkin lymphoma", "shortest_name_length": 21}
{"curie": "MONDO:0010821", "names": ["FOXP2-associated dysphasia", "specific language impairment", "Billard Toutain Maheut syndrome", "Billard-Toutain-Maheut syndrome", "developmental language disorder", "developmental dysphasia familial", "familial developmental dysphasia", "Familial developmental dysphasia", "DYSPHASIA, FAMILIAL DEVELOPMENTAL", "Dysphasia, Familial Developmental", "dysphasia, familial developmental", "Familial developmental dysphasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial developmental dysphasia", "shortest_name_length": 26}
{"curie": "UMLS:C0268671", "names": ["nonalcoholic; Korsakov", "Korsakov; nonalcoholic", "non-AODR Korsakoff's syndrome", "Korsakoffs psychosis;non-alcoh", "Non-alcoholic amnestic syndrome", "nonalcoholic Korsakoff's syndrome", "Non-alcoholic Korsakoff psychosis", "Korsakoff's nonalcoholic psychosis", "non-alcoholic Korsakoff's syndrome", "nonalcoholic polyneuritic psychosis", "Korsakov's syndrome - non-alcoholic", "Non-alcoholic Korsakoff's psychosis", "Korsakoff's psychosis non-alcoholic", "Korsakoff's psychosis, non-alcoholic", "Korsakoff's syndrome - non-alcoholic", "Korsakoff's psychosis (non-alcoholic)", "nonalcoholic Wernicke-Korsakoff syndrome", "nonalcoholic Wernicke-Korsakoff psychosis", "Korsakov's psychosis or syndrome, nonalcoholic", "Non-alcoholic Korsakoff's psychosis (disorder)", "non-alcoholic Korsakoff's syndrome (diagnosis)", "non-Alcohol or Other Drug Related Korsakoff's syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-alcoholic Korsakoff's psychosis", "shortest_name_length": 22}
{"curie": "UMLS:C4726544", "names": ["Myeloid Neoplasms with Germline RUNX1 Mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myeloid Neoplasms with Germline RUNX1 Mutation", "shortest_name_length": 46}
{"curie": "UMLS:C0919591", "names": ["Urogenital bleeding", "Bleeding urogenital", "Urogenital hemorrhage", "Urogenital haemorrhage", "genitourinary; hemorrhage", "hemorrhage; genitourinary", "Genitourinary tract hemorrhage", "Genitourinary tract haemorrhage", "Genitourinary tract hemorrhage (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Genitourinary tract hemorrhage", "shortest_name_length": 19}
{"curie": "UMLS:C1275214", "names": ["Cylindrocarcinoma", "Malignant cylindroma", "Malignant Cylindroma", "Carcinoma ex Cylindroma", "Malignant dermal cylindroma", "malignant cylindroma of skin", "Malignant cylindroma of skin", "Malignant cylindroma of skin (disorder)", "malignant cylindroma of skin (diagnosis)", "Malignant cylindroma of skin (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant cylindroma", "shortest_name_length": 17}
{"curie": "MONDO:0034978", "names": ["isolated foveal hypoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated foveal hypoplasia", "shortest_name_length": 26}
{"curie": "UMLS:C0159658", "names": ["fracture clavicle", "CLAVICLE FRACTURE", "Broken collarbone", "Clavicle fracture", "broken collarbone", "Fracture;clavicle", "Clavicle Fracture", "collarbone broken", "clavicle fracture", "Fractured clavicle", "clavicle; fracture", "clavicle fractures", "fractured clavicle", "fracture; clavicle", "CLAVICULAR FRACTURE", "clavicular fracture", "fracture collar bone", "collar bone fracture", "fracture of clavicle", "Fracture of clavicle", "Collar bone fracture", "clavicular fractures", "bone collar fracture", "Clavicular fractures", "fractured collar bone", "bone collar fractures", "Fractured collar bone", "fracture; collar bone", "collar bone; fracture", "bone collar fractured", "Fracture of collar bone", "Fracture of clavicle, NOS", "Fracture of clavicle (disorder)", "fracture of clavicle (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fracture of clavicle", "shortest_name_length": 17}
{"curie": "UMLS:C0334238", "names": ["fusiform type SCLC", "SCLC, fusiform type", "fusiform type small cell carcinoma", "small cell carcinoma, fusiform cell", "Small cell carcinoma, fusiform cell", "Small cell carcinoma - fusiform cell", "fusiform type small cell lung cancer", "small cell lung cancer, fusiform type", "Small Cell Cancer, Fusiform Cell Type", "lung cancer, fusiform type, small cell", "Small Cell Carcinoma, Fusiform Cell Type", "Small cell carcinoma, fusiform cell type", "fusiform type small cell carcinoma (diagnosis)", "Small cell carcinoma, fusiform cell (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small cell carcinoma, fusiform cell", "shortest_name_length": 18}
{"curie": "UMLS:C1333943", "names": ["Head and Neck Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Head and Neck Infection", "shortest_name_length": 23}
{"curie": "MONDO:0033635", "names": ["MC4DN3", "mitochondrial complex 4 deficiency, nuclear type 3", "MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 3", "mitochondrial complex IV deficiency, nuclear type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 4 deficiency, nuclear type 3", "shortest_name_length": 6}
{"curie": "MONDO:0014076", "names": ["DKCB5", "DKCA4", "autosomal recessive dyskeratosis congenita 5", "Dyskeratosis Congenita, Autosomal Dominant 4", "DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 4", "dyskeratosis congenita, autosomal dominant 4", "dyskeratosis congenita, autosomal recessive 5", "DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 5", "Dyskeratosis Congenita, Autosomal Recessive 5", "dyskeratosis congenita, autosomal recessive type 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyskeratosis congenita, autosomal recessive 5", "shortest_name_length": 5}
{"curie": "UMLS:C0349725", "names": ["Graft infection", "graft infection", "graft infections", "grafts infections", "infection of graft", "Graft infection (disorder)", "infection of graft (diagnosis)", "complications of graft infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Graft infection", "shortest_name_length": 15}
{"curie": "UMLS:C1299579", "names": ["cirrhosis early", "Early cirrhosis", "Early cirrhosis (disorder)", "Early cirrhosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Early cirrhosis", "shortest_name_length": 15}
{"curie": "MONDO:0009879", "names": ["Kowarski syndrome", "KOWARSKI syndrome", "KOWARSKI SYNDROME", "Pituitary dwarfism 4", "Biodefective Growth hormone", "BIODEFECTIVE GROWTH HORMONE", "Nanism due to growth hormone qualitative anomaly", "short stature due to growth hormone qualitative anomaly", "Short stature due to growth hormone qualitative anomaly", "Pituitary dwarfism with normal immunoreactive growth hormone", "Pituitary Dwarfism With Normal Immunoreactive Growth Hormone And Low Somatomedin", "PITUITARY DWARFISM WITH NORMAL IMMUNOREACTIVE GROWTH HORMONE AND LOW SOMATOMEDIN", "pituitary dwarfism with normal immunoreactive Growth hormone and Low Somatomedin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short stature due to growth hormone qualitative anomaly", "shortest_name_length": 17}
{"curie": "UMLS:C0153685", "names": ["Renal Metastasis", "renal metastasis", "Renal Metastases", "Renal metastases", "Renal metastasis", "kidney metastasis", "kidney metastases", "Metastases to Kidney", "Metastasis to Kidney", "Metastasis to kidney", "Metastases to kidney", "Secondary renal cancer", "secondary kidney cancer", "metastasis to the kidney", "Metastasis to the Kidney", "Metastases to the Kidney", "Metastatic tumor in kidney", "Secondary cancer of kidney", "Cancer metastatic to kidney", "Metastatic tumour in kidney", "Metastatic Tumor to the Kidney", "Metastasis to renal parenchyma", "Metastatic Neoplasm to the Kidney", "kidney malignant neoplasm secondary", "Secondary malignant neoplasm of kidney", "Metastatic malignant neoplasm to kidney", "Metastatic malignant neoplasm of kidney", "metastasis of malignant neoplasm to kidney", "Metastatic Malignant Neoplasm to the Kidney", "Metastatic Malignant Neoplasm in the Kidney", "Secondary malignant neoplasm of kidney, NOS", "Metastatic malignant neoplasm to kidney, NOS", "Metastatic malignant neoplasm to kidney (disorder)", "Secondary malignant neoplasm of kidney (diagnosis)", "metastasis of malignant neoplasm to kidney (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to kidney", "shortest_name_length": 16}
{"curie": "MONDO:0032924", "names": ["CILD45", "primary ciliary dyskinesia 45", "ciliary dyskinesia, primary, 45", "CILIARY DYSKINESIA, PRIMARY, 45", "primary ciliary dyskinesia 45 without situs inversus", "CILIARY DYSKINESIA, PRIMARY, 45, WITHOUT SITUS INVERSUS", "Ciliary Dyskinesia, Primary, 45, Without Situs Inversus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ciliary dyskinesia, primary, 45", "shortest_name_length": 6}
{"curie": "MONDO:0007812", "names": ["ADLI", "Lamellar ichthyosis, dominant", "Autosomal-dominant lamellar ichthyosis", "Autosomal dominant lamellar ichthyosis", "ichthyosis lamellar autosomal dominant", "ichthyosis lamellar, autosomal dominant", "LAMELLAR ICHTHYOSIS, AUTOSOMAL DOMINANT", "Lamellar Ichthyosis, Autosomal Dominant", "lamellar ichthyosis, autosomal dominant", "ICHTHYOSIS, LAMELLAR, AUTOSOMAL DOMINANT", "Ichthyosis, Lamellar, Autosomal Dominant", "ichthyosis, lamellar, autosomal dominant", "Lamellar ichthyosis, autosomal dominant form", "Autosomal dominant lamellar ichthyosis (disorder)", "Autosomal dominant lamellar ichthyosis (diagnosis)", "Ichthyosiform erythroderma, nonbullous, dominant form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ichthyosis, lamellar, autosomal dominant", "shortest_name_length": 4}
{"curie": "MONDO:0043364", "names": ["EPXD", "PRESENTEY ANOMALY", "Presentey Anomaly", "presentey anomaly", "Presentey anomaly", "eosinophil peroxidase deficiency", "EOSINOPHIL PEROXIDASE DEFICIENCY", "Eosinophil peroxidase deficiency", "eosinophil peroxidase deficiency, partial", "eosinophil peroxidase deficiency, Partial", "EOSINOPHIL PEROXIDASE DEFICIENCY, PARTIAL", "Eosinophil Peroxidase Deficiency, Partial", "Eosinophil peroxidase deficiency (disorder)", "eosinophil peroxidase deficiency (diagnosis)", "Peroxidase and Phospholipid Deficiency in Eosinophils", "Peroxidase and phospholipid deficiency in eosinophils", "peroxidase and phospholipid deficiency in eosinophils", "PEROXIDASE AND PHOSPHOLIPID DEFICIENCY IN EOSINOPHILS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eosinophil peroxidase deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0016965", "names": ["Trisomy 15q", "15q trisomy", "trisomy 15q", "15q+ syndrome", "15q duplication", "Duplication 15q", "dup(15q) syndrome", "partial trisomy 15q", "chromosome 15q trisomy", "Chromosome 15q, trisomy", "duplication 15q syndrome", "15q duplication syndrome", "chromosome 15q duplication", "partial trisomy of chromosome 15q", "chromosome 15q duplication syndrome", "partial duplication of chromosome 15q", "partial trisomy of the long arm of chromosome 15", "partial duplication of the long arm of chromosome 15", "partial duplication of the long arm of chromosome type 15"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of the long arm of chromosome 15", "shortest_name_length": 11}
{"curie": "MONDO:0018384", "names": ["genetic avascular necrosis", "avascular necrosis of genetic origin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "avascular necrosis of genetic origin", "shortest_name_length": 26}
{"curie": "MONDO:0100085", "names": ["cancer of fore limb long bone", "long bones of upper limb cancer", "cancer of long bone of forelimb", "cancer of long bone of fore limb", "cancer of long bone of upper limb", "cancer of upper extremity long bone", "cancer of long bone of upper extremity", "malignant upper limb long bone neoplasm", "malignant neoplasm of upper limb long bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cancer of long bone of upper limb", "shortest_name_length": 29}
{"curie": "UMLS:C1333106", "names": ["Colorectal Adenoma with Mild Dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Adenoma with Mild Dysplasia", "shortest_name_length": 38}
{"curie": "MONDO:0019871", "names": ["Trisomy 2pter", "trisomy 2pter", "Distal trisomy 2p", "Distal Trisomy 2p", "distal trisomy 2p", "distal duplication 2p", "Distal duplication 2p", "distal trisomy type 2p", "telomeric duplication 2p", "Telomeric duplication 2p", "Distal trisomy 2p (disorder)", "Distal trisomy 2p (diagnosis)", "anomaly of chromosome pair distal trisomy 2p"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal trisomy 2p", "shortest_name_length": 13}
{"curie": "UMLS:C2348376", "names": ["Ectopic Supraventricular Rhythm", "Ectopic Supraventricular Rhythm by EKG Finding", "Ectopic Supraventricular Rhythm by ECG Finding"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ectopic Supraventricular Rhythm by ECG Finding", "shortest_name_length": 31}
{"curie": "UMLS:C2919902", "names": ["Chemical pregnancy", "Chemical Pregnancy", "Peri-Implantational Loss", "Peri-Implantational Failure", "Chemical pregnancy (disorder)", "Chemical pregnancy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chemical pregnancy", "shortest_name_length": 18}
{"curie": "UMLS:C5666821", "names": ["fHP", "Fibrotic Hypersensitivity Pneumonitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fibrotic Hypersensitivity Pneumonitis", "shortest_name_length": 3}
{"curie": "MONDO:0100131", "names": ["PARDS", "pediatric acute respiratory distress syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pediatric acute respiratory distress syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0022821", "names": ["congenital benign spinal muscular atrophy dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital benign spinal muscular atrophy dominant", "shortest_name_length": 50}
{"curie": "MONDO:0015921", "names": ["ARX-related epileptic encephalopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ARX-related epileptic encephalopathy", "shortest_name_length": 36}
{"curie": "MONDO:0034901", "names": ["ATP13A2-related parkinsonism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ATP13A2-related parkinsonism", "shortest_name_length": 28}
{"curie": "UMLS:C5239071", "names": ["Unresectable Angiosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Angiosarcoma", "shortest_name_length": 25}
{"curie": "MONDO:0003545", "names": ["Intradural Extramedullary Spinal tumors", "Intradural Extramedullary Spinal Tumors", "intradural extramedullary spinal tumors", "Intradural Extramedullary Spinal Neoplasms", "intradural extramedullary spinal neoplasms", "Intradural Extramedullary Spinal Canal Tumor", "intradural extramedullary spinal canal tumor", "intradural extramedullary spinal canal tumors", "Intradural Extramedullary Spinal Canal Tumors", "intradural extramedullary spinal canal neoplasm", "spinal canal intradural extramedullary neoplasm", "Intradural Extramedullary Tumor of Spinal Canal", "intradural extramedullary tumor of spinal canal", "Intradural Extramedullary Spinal Canal Neoplasm", "intradural extramedullary neoplasm of spinal canal", "Intradural Extramedullary Neoplasm of Spinal Canal", "Intradural Extramedullary Tumor of the Spinal Canal", "intradural extramedullary tumor of the spinal canal", "intradural extramedullary neoplasm of the spinal canal", "Intradural Extramedullary Neoplasm of the Spinal Canal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intradural extramedullary spinal canal neoplasm", "shortest_name_length": 39}
{"curie": "MONDO:0001395", "names": ["Macular keratitis", "macular keratitis", "Macular keratitis (disorder)", "macular keratitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macular keratitis", "shortest_name_length": 17}
{"curie": "MONDO:0006032", "names": ["CYSTITIS", "cystitis", "Cystitis", "CYSTALGIA", "Cystalgia", "Cystitides", "Urocystitis", "Cystitis NOS", "Cystitis, NOS", "CYSTITIS (NOS)", "infection bladder", "bladder infection", "Bladder infection", "Cystitis (disorder)", "Bladder inflammation", "cystitis (diagnosis)", "bladder inflammation", "bladder; inflammation", "inflammation; bladder", "Cystitis, unspecified", "inflammation of bladder", "Inflammation of bladder", "Urinary bladder inflamed", "Urinary bladder inflammation", "urinary bladder inflammation", "Bladder infection (diagnosis)", "inflammation of urinary bladder", "Cystitis of the urinary bladder", "Inflammation of urinary bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cystitis", "shortest_name_length": 8}
{"curie": "MONDO:0016846", "names": ["distal dup(22)(q11.2)", "Distal dup(22)(q11.2)", "distal trisomy 22q11.2", "Distal trisomy 22q11.2", "distal 22q11.2 microduplication syndrome", "Distal 22q11.2 microduplication syndrome", "Distal 22q11.2 microduplication syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal 22q11.2 microduplication syndrome", "shortest_name_length": 21}
{"curie": "UMLS:C0010543", "names": ["cyclitis", "Cyclitis", "Cyclitis, NOS", "Cyclitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cyclitis", "shortest_name_length": 8}
{"curie": "MONDO:0012599", "names": ["HYT8", "HYPERTENSION, ESSENTIAL, SUSCEPTIBILITY TO, 8", "hypertension, essential, susceptibility to, 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertension, essential, susceptibility to, 8", "shortest_name_length": 4}
{"curie": "UMLS:C1332505", "names": ["Benign Germ Cell Tumor", "Benign Tumor of Germ Cell", "Benign Germ Cell Neoplasm", "Benign germ cell neoplasm", "Benign Neoplasm of Germ Cell", "Benign Tumor of the Germ Cell", "Benign Neoplasm of the Germ Cell", "Benign germ cell neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign germ cell neoplasm", "shortest_name_length": 22}
{"curie": "UMLS:C0685835", "names": ["INCREASED ANOGENITAL DISTANCE", "Anogenital Distance Increased", "Increased anogenital distance", "Increased anogenital distance (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Increased anogenital distance", "shortest_name_length": 29}
{"curie": "MONDO:0022397", "names": ["retinal ciliopathy due to mutation in the retinitis pigmentosa-1 gene"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal ciliopathy due to mutation in the retinitis pigmentosa-1 gene", "shortest_name_length": 69}
{"curie": "MONDO:0017478", "names": ["amelia of upper limb, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amelia of upper limb, unilateral", "shortest_name_length": 32}
{"curie": "MONDO:0100029", "names": ["antibody mediated epilepsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "antibody mediated epilepsy", "shortest_name_length": 26}
{"curie": "MONDO:0009288", "names": ["Gsd1C", "GSD1D", "GSD1B", "GSD1d", "GSD1C", "GSDIb", "GSD Ib", "GSD Ic", "GSD type 1b", "GSD type IB", "GSD type Ic", "GSD type Ib", "G6PT deficiency", "GSD type 1 non a", "glycogenosis type IB", "glycogenosis type 1b", "Glycogenosis type 1b", "Glycogenosis type Ib", "G6P deficiency type IB", "G6P deficiency type Ib", "Glucose transport defect", "G6P translocase deficiency", "Phosphate transport defect", "GSD due to G6PT deficiency", "Glycogen Storage Disease IC", "GLYCOGEN STORAGE DISEASE Id", "glycogen storage disease Ib", "GLYCOGEN STORAGE DISEASE Ib", "glycogen storage disease Ic", "Glycogen Storage Disease IB", "GLYCOGEN STORAGE DISEASE Ic", "Glycogen Storage Disease Id", "glycogen storage disease type Ic", "Glycogen storage disease type Ib", "Glycogen storage disease type IB", "Glycogen Storage Disease Type Ib", "Glycogen storage disease type Id", "Glycogen storage disease type 1b", "Glycogen storage disease type Ic", "glycogen storage disease type IB", "glycogen storage disease type 1b", "GSD due to G6P deficiency type 1b", "GSD due to G6P deficiency type IB", "GSD due to G6P deficiency type Ib", "von Gierke's disease (GSD type IB)", "Glucose transport defect (disorder)", "glucose-6-phosphate transport defect", "Glucose-6-Phosphate Transport Defect", "Glucose 6-phosphate transport defect", "GLUCOSE-6-PHOSPHATE TRANSPORT DEFECT", "Glucose-6-phosphate transport defect", "Phosphate transport defect (disorder)", "glycogen storage disease type I non-a", "Glycogen Storage Disease Type I non-a", "Glycogen storage disease type Ic (diagnosis)", "von Gierke's disease (GSD type IB) (diagnosis)", "Glucose-6-phosphate transport defect (disorder)", "Glycogen storage disease due to G6P deficiency type Ib", "glycogen storage disease due to G6P deficiency type IB", "Glycogenosis due to glucose-6-phosphatase deficiency type 1b", "glycogenosis due to glucose-6-phosphatase deficiency type 1B", "Glycogenosis due to glucose-6-phosphatase transport defect type Ib", "glycogenosis due to glucose-6-phosphatase transport defect type IB", "Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease Ib", "shortest_name_length": 5}
{"curie": "UMLS:C0600177", "names": ["Low Cardiac Output Syndrome", "Low cardiac output syndrome", "Low cardiac output syndrome (disorder)", "Low cardiac output syndrome (diagnosis)", "heart failure low cardiac output syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Cardiac Output Syndrome", "shortest_name_length": 27}
{"curie": "MONDO:0004585", "names": ["hydramnios", "HYDRAMNIOS", "Hydramnios", "POLYHYDRAMNIOS", "hydrops; amnii", "Polyhydramnios", "Hydrops amnion", "polyhydramnios", "Excessive liquor", "Hydrops of amnion", "pregnancy; hydramnios", "pregnancy; hydrops amnii", "polyhydramnios (disease)", "Polyhydramnios (disorder)", "pregnancy; polyhydramnios", "polyhydramnios (diagnosis)", "Hydrops of amnion (diagnosis)", "High levels of amniotic fluid", "Amniotic fluid index increased", "Increased amniotic fluid index", "placental disorders hydrops of amnion", "pregnancy; amniotic fluid, disorder, polyhydramnios"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyhydramnios", "shortest_name_length": 10}
{"curie": "MONDO:0006497", "names": ["CP", "Palsy cerebral", "Cerebral palsy", "cerebral palsy", "CEREBRAL PALSY", "Palsy;cerebral", "Cerebral Palsy", "PALSY CEREBRAL", "PALSY, CEREBRAL", "Cerebral palsied", "cerebral paralysis", "Cerebral paralysis", "Cerebral palsy NOS", "Cerebral palsy (CP)", "Cerebral palsy, NOS", "paralysis; cerebral", "CP (Cerebral Palsy)", "CP - Cerebral palsy", "cerebral; paralysis", "Infantile cerebral palsy", "infantile cerebral palsy", "Congenital cerebral palsy", "Cerebral palsy (disorder)", "cerebral palsy (diagnosis)", "cerebral palsy unspecified", "Cerebral palsy, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral palsy", "shortest_name_length": 2}
{"curie": "MONDO:0008665", "names": ["Tucker syndrome", "tucker syndrome", "ptosis vocal cord paralysis", "Ptosis vocal cord paralysis", "VOCAL CORD PARALYSIS AND PTOSIS", "vocal cord paralysis and ptosis", "Vocal Cord Paralysis And Ptosis", "Ptosis-vocal cord paralysis syndrome", "ptosis-vocal cord paralysis syndrome", "Ptosis and vocal cord paralysis syndrome", "Ptosis and vocal cord paralysis syndrome (disorder)", "Congenital bilateral recurrent nerve paralysis and ptosis", "congenital bilateral recurrent nerve paralysis and ptosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ptosis-vocal cord paralysis syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0000661", "names": ["alexithymia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alexithymia", "shortest_name_length": 11}
{"curie": "UMLS:C4054393", "names": ["Nephrotic Syndrome - COQ6 Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - COQ6 Associated", "shortest_name_length": 36}
{"curie": "MONDO:0013437", "names": ["RP43", "RETINITIS PIGMENTOSA 43", "retinitis pigmentosa 43", "PDE6A retinitis pigmentosa", "retinitis pigmentosa type 43", "retinitis pigmentosa caused by mutation in PDE6A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 43", "shortest_name_length": 4}
{"curie": "MONDO:0043303", "names": ["phonophobia", "hyperacusia", "Hyperacusis", "Hyperacusia", "hyperacuses", "Hyperacuses", "hyperacusis", "HYPERACUSIS", "hyperacusias", "Phonophobias", "Hyperacusias", "Sensitivity to noise", "Auditory hyperacuity", "AUDITORY HYPERACUITY", "Loudness intolerance", "Loudness Recruitment", "Loudness recruitment", "loudness recruitment", "Recruitment, Loudness", "Oversensitive hearing", "recruitment, loudness", "oversensitive hearing", "Loudness Recruitments", "loudness Recruitments", "low tolerance to sound", "Hyperacusis (disorder)", "auditory hyperesthesia", "hyperesthesia, auditory", "auditory Hyperesthesias", "hyperacusis (diagnosis)", "Hearing abnormally acute", "hyperesthesias, auditory", "HEARING ABNORMALLY ACUTE", "sounds seem unnaturally loud", "Sounds seem unnaturally loud", "very sensitive to loud sounds", "Painful sensitiveness to sound", "PAINFUL SENSITIVENESS TO SOUND", "Loudness recruitment (finding)", "Loudness Perception Disturbance", "loudness perception disturbance", "Perception Disturbance, Loudness", "Loudness Perception Disturbances", "Disturbance, Loudness Perception", "disturbance, loudness perception", "loudness perception disturbances", "perception disturbance, loudness", "perception disturbances, loudness", "Disturbances, Loudness Perception", "Perception Disturbances, Loudness", "disturbances, loudness perception", "very sensitive to loud sounds (symptom)", "very sensitive to loud sounds (hyperacusis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperacusis", "shortest_name_length": 11}
{"curie": "MONDO:0018590", "names": ["Aβ2M amyloidosis", "Amyloidosis Beta2M", "ABeta2M amyloidosis", "dialysis-related amyloidosis", "Beta2-microglobulinic amyloidosis", "dialysis-related beta2-microglobulin amyloidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ABeta2M amyloidosis", "shortest_name_length": 16}
{"curie": "MONDO:0009915", "names": ["pseudohermaphroditism, female, with skeletal anomalies", "PSEUDOHERMAPHRODITISM, FEMALE, WITH SKELETAL ANOMALIES", "Pseudohermaphroditism, Female, with Skeletal Anomalies", "female pseudohermaphroditism-skeletal anomalies syndrome", "46,XX disorder of sex development-skeletal anomalies syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XX disorder of sex development-skeletal anomalies syndrome", "shortest_name_length": 54}
{"curie": "UMLS:C0861555", "names": ["Oral neoplasm malignant recurrent", "Recurrent Malignant Oral Neoplasm", "Recurrent Malignant Lip and Oral Cavity Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral neoplasm malignant recurrent", "shortest_name_length": 33}
{"curie": "UMLS:C1328337", "names": ["Urethritis noninfective"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urethritis noninfective", "shortest_name_length": 23}
{"curie": "MONDO:0000771", "names": ["airway allergy", "respiratory allergy", "allergic respiratory disease", "allergic respiratory system disease", "allergic form of respiratory system disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "allergic respiratory disease", "shortest_name_length": 14}
{"curie": "MONDO:0003033", "names": ["prostate angiosarcoma", "Prostate Angiosarcoma", "Prostatic Angiosarcoma", "prostatic angiosarcoma", "Angiosarcoma of Prostate", "prostate hemangiosarcoma", "Prostate Hemangiosarcoma", "angiosarcoma of prostate", "prostatic hemangiosarcoma", "Prostatic Hemangiosarcoma", "Prostatic hemangiosarcoma", "Hemangiosarcoma of Prostate", "hemangiosarcoma of prostate", "angiosarcoma of the prostate", "Angiosarcoma of the Prostate", "Hemangiosarcoma of the Prostate", "hemangiosarcoma of the prostate", "prostate gland angiosarcoma (disease)", "angiosarcoma (disease) of prostate gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate angiosarcoma", "shortest_name_length": 21}
{"curie": "MONDO:0007201", "names": ["BPES", "BPES type I", "BPES type 1", "BPES, type 1", "BPES, type 2", "BPES type II", "BPES, TYPE I", "BPES syndrome", "BPES, TYPE II", "BPES WITH OVARIAN FAILURE", "Bpes With Ovarian Failure", "blepharophimosis sequence", "blepharophimosis syndrome", "BPES with ovarian failure", "Blepharophimosis Syndrome", "Blepharophimosis syndrome", "BPES WITHOUT OVARIAN FAILURE", "BPES without ovarian failure", "Bpes Without Ovarian Failure", "blepharophimosis types 1 and 2", "blepharophimosis syndrome type 1", "BPES, type I, autosomal recessive", "Conjunctival eyelid tetra syndrome", "Familial blepharophimosis syndrome", "BPES with Duane retraction syndrome", "Bpes With Duane Retraction Syndrome", "BPES with premature ovarian failure", "BPES WITH DUANE RETRACTION SYNDROME", "Blepharophimosis, Ptosis, and Epicanthus Inversus", "BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS", "blepharophimosis, ptosis, and epicanthus inversus", "Blepharophimosis-ptosis-epicanthus inversus syndrome", "blepharophimosis-ptosis-epicanthus inversus syndrome", "blepharophimosis-epicanthus inversus-ptosis syndrome", "Blepharophimosis epicanthus inversus ptosis syndrome", "blepharophimosis, ptosis, epicanthus inversus syndrome", "Blepharophimosis, ptosis, epicanthus inversus syndrome", "Blepharophimosis, Ptosis, and Epicanthus Inversus Type I", "BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS, TYPE I", "blepharophimosis, epicanthus inversus, and ptosis, type 2", "blepharophimosis, epicanthus inversus, and ptosis, type 1", "blepharophimosis, ptosis, and epicanthus inversus syndrome", "Blepharophimosis, ptosis, and epicanthus inversus syndrome", "Blepharophimosis, Ptosis, and Epicanthus Inversus Syndrome", "BPES - blepharophimosis epicanthus inversus ptosis syndrome", "blepharophimosis-ptosis-epicanthus inversus-telecanthus complex", "Blepharophimosis epicanthus inversus ptosis syndrome (disorder)", "hereditary blepharophimosis-ptosis-epicanthus inversus syndrome", "blepharophimosis, ptosis, and epicanthus inversus syndrome type 1", "blepharophimosis, ptosis, epicanthus inversus with ovarian failure", "blepharophimosis-ptosis-epicanthus inversus (BPEI) syndrome (BPES)", "blepharophimosis-ptosis-epicanthus inversus-primary amenorrhea syndrome", "blepharoptosis-blepharophimosis-epicanthus inversus-telecanthus syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blepharophimosis, ptosis, and epicanthus inversus syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0016674", "names": ["46,XY PGD", "46,XY partial gonadal dysgenesis", "46,XY partial testicular dysgenesis", "46,XY partial gonadal dysgenesis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XY partial gonadal dysgenesis", "shortest_name_length": 9}
{"curie": "MONDO:0009966", "names": ["MKS7", "Goldston syndrome", "Meckel syndrome 7", "GOLDSTON SYNDROME", "Meckel-Like Syndrome", "Meckel like syndrome", "Meckel syndrome type 7", "MECKEL SYNDROME, TYPE 7", "Meckel syndrome, type 7", "Meckel-like syndrome type 1", "Meckel-Gruber syndrome, type 7", "NPHP3-related Meckel-like syndrome", "Meckel syndrome type 7 (diagnosis)", "Nephrocystin 3-related Meckel-like syndrome", "NPHP3 (nephrocystin 3) related Meckel-like syndrome", "Renal hepatic pancreatic dysplasia Dandy Walker cyst", "Nephrocystin 3-related Meckel-like syndrome (disorder)", "Dandy-Walker cyst with renal-hepatic-pancreatic dysplasia", "Renal-Hepatic-Pancreatic Dysplasia with Dandy-Walker Cyst", "RENAL-HEPATIC-PANCREATIC DYSPLASIA WITH DANDY-WALKER CYST", "renal-hepatic-pancreatic dysplasia with Dandy-Walker cyst", "Renal-hepatic-pancreatic dysplasia-Dandy-Walker cysts syndrome", "renal-hepatic-pancreatic dysplasia-Dandy-Walker cysts syndrome", "Renal, hepatic, pancreatic dysplasia, Dandy-Walker cysts syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "NPHP3-related Meckel-like syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0016381", "names": ["congenital hypertrichosis", "hypertrichosis universalis", "HYPERTRICHOSIS UNIVERSALIS", "Hypertrichosis universalis", "HYPERTRICHOSIS LANUGINOSA CONGENITA", "hypertrichosis lanuginosa congenita", "Hypertrichosis lanuginosa congenita", "congenital hypertrichosis lanuginosa", "Hypertrichosis universalis congenita", "Congenital hypertrichosis lanuginosa", "Hypertrichosis lanuginosa universalis", "Hypertrichosis universalis (disorder)", "hypertrichosis lanuginosa universalis", "Congenital hypertrichosis lanuginosa (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrichosis lanuginosa congenita", "shortest_name_length": 25}
{"curie": "UMLS:C1336275", "names": ["Stage III Thyroid Papillary Carcinoma", "Stage III Papillary Carcinoma of Thyroid", "Stage III Thyroid Gland Papillary Cancer", "Stage III Thyroid Gland Papillary Carcinoma", "Stage III Papillary Thyroid Gland Carcinoma", "Stage III Papillary Carcinoma of the Thyroid", "Stage III Papillary Carcinoma of Thyroid Gland", "Stage III Papillary Carcinoma of the Thyroid Gland", "Stage III Thyroid Gland Papillary Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Thyroid Gland Papillary Carcinoma AJCC v7", "shortest_name_length": 37}
{"curie": "MONDO:0013890", "names": ["CNM4", "centronuclear myopathy 4", "MYOPATHY, CENTRONUCLEAR 4", "MYOPATHY, CENTRONUCLEAR, 4", "myopathy, centronuclear, 4", "Centronuclear myopathy type 4", "centronuclear myopathy type 4", "myopathy, centronuclear, type 4", "Congenital myopathy with internal nuclei and atypical cores", "congenital myopathy with internal nuclei and atypical cores", "Congenital myopathy with internal nuclei and atypical cores (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myopathy with internal nuclei and atypical cores", "shortest_name_length": 4}
{"curie": "UMLS:C0399408", "names": ["Abnormal pulp hard tissue", "Hard tissue formation in pulp", "Abnormal hard tissue formation in pulp", "Abnormal Hard Tissue Formation in Pulp", "abnormal hard tissue formation in pulp of tooth", "pulp (dental); abnormal formation of hard tissue", "Abnormal hard tissue formation in pulp (disorder)", "abnormal hard tissue formation in pulp of tooth (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abnormal hard tissue formation in pulp", "shortest_name_length": 25}
{"curie": "MONDO:0033667", "names": ["DELMNES", "Delpire-McNeill syndrome", "DELPIRE-MCNEILL SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Delpire-McNeill syndrome", "shortest_name_length": 7}
{"curie": "MONDO:0011836", "names": ["Hurthle cell thyroid cancer", "Thyroid cancer, Hurthle cell", "thyroid cancer, Hurthle cell", "Hurthle cell thyroid neoplasia", "thyroid Hurthle cell carcinoma", "thyroid carcinoma, Hurthle cell", "oncocytic carcinoma of the thyroid", "thyroid gland Hurthle cell carcinoma", "follicular thyroid cancer, Hurthle cell type", "thyroid cancer, follicular, Hurthle cell type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid Hurthle cell carcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C4528580", "names": ["Stage II Breast Cancer", "Prognostic Stage II Breast Cancer AJCC v8", "Prognostic Stage II Breast Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prognostic Stage II Breast Cancer AJCC v8", "shortest_name_length": 22}
{"curie": "UMLS:C0948266", "names": ["latent tetany", "Latent tetany"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Latent tetany", "shortest_name_length": 13}
{"curie": "UMLS:C1504411", "names": ["Post procedural edema", "Post procedural oedema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post procedural edema", "shortest_name_length": 21}
{"curie": "UMLS:C1335426", "names": ["Plasma Cell PTLD", "Plasma Cell Post-Transplant Lymphoproliferative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Plasma Cell Post-Transplant Lymphoproliferative Disorder", "shortest_name_length": 16}
{"curie": "MONDO:0019630", "names": ["congenital ectropion uveae"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital ectropion uveae", "shortest_name_length": 26}
{"curie": "MONDO:0009331", "names": ["IH", "HHP", "hemi-3 syndrome", "hemihypertrophy", "HEMIHYPERPLASIA", "HEMI-3 SYNDROME", "hemi 3 syndrome", "hemihyperplasia", "Hemihyperplasia", "Hemi 3 Syndrome", "Hemi 3 syndrome", "isolated hemihypertrophy", "Isolated hemihyperplasia", "Hemicorporal hypertrophy", "Isolated hemihypertrophy", "isolated hemihyperplasia", "Hemihyperplasia, Isolated", "hemihypertrophy, isolated", "HEMIHYPERPLASIA, ISOLATED", "HEMIHYPERTROPHY, ISOLATED", "Hemihypertrophy, Isolated", "hemihyperplasia, isolated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated hemihyperplasia", "shortest_name_length": 2}
{"curie": "UMLS:C5447532", "names": ["ALT/WDLPS of Deep Soft Tissue", "Well-Differentiated Liposarcoma of Deep Soft Tissue", "Well Differentiated Liposarcoma of Deep Soft Tissue", "Atypical Lipomatous Tumor/Well Differentiated Liposarcoma of Deep Soft Tissue", "Atypical Lipomatous Tumor/Well-Differentiated Liposarcoma of Deep Soft Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypical Lipomatous Tumor/Well Differentiated Liposarcoma of Deep Soft Tissue", "shortest_name_length": 29}
{"curie": "UMLS:C1336443", "names": ["Ureter Cancer Stage IV", "Stage IV Ureter Cancer", "Stage IV Ureter Carcinoma", "Stage IV Ureteral Carcinoma", "Stage IV Carcinoma of Ureter", "Stage IV Ureter Cancer AJCC v7", "Stage IV Carcinoma of the Ureter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Ureter Cancer AJCC v7", "shortest_name_length": 22}
{"curie": "UMLS:C0018675", "names": ["head neoplasm", "Head Neoplasm", "Neoplasm, Head", "Head Neoplasms", "Neoplasms, Head", "neoplasm of head", "Neoplasm of head", "Neoplasm of head (disorder)", "neoplasm of head (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Head Neoplasms", "shortest_name_length": 13}
{"curie": "UMLS:C4683782", "names": ["Plasma Cell Myeloma by RISS Stage", "Plasma Cell Myeloma by Revised International Staging System Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Plasma Cell Myeloma by RISS Stage", "shortest_name_length": 33}
{"curie": "MONDO:0044717", "names": ["proximal del(4)(q25)", "proximal monosomy 4q25", "4q25 proximal deletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "4q25 proximal deletion syndrome", "shortest_name_length": 20}
{"curie": "MONDO:0015786", "names": ["Prader-Willi syndrome due to imprinting mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prader-Willi syndrome due to imprinting mutation", "shortest_name_length": 48}
{"curie": "MONDO:0019892", "names": ["monosomy 7pter", "distal deletion 7p", "distal monosomy 7p", "telomeric deletion 7p", "distal monosomy type 7p"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal monosomy 7p", "shortest_name_length": 14}
{"curie": "UMLS:C4524462", "names": ["Oral Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral Intraepithelial Neoplasia", "shortest_name_length": 30}
{"curie": "MONDO:0016944", "names": ["7p trisomy", "trisomy 7p", "Trisomy 7p", "7p+ syndrome", "7p duplication", "Duplication 7p", "dup(7p) syndrome", "7p partial trisomy", "partial trisomy 7p", "chromosome 7p trisomy", "7p duplication syndrome", "duplication 7p syndrome", "Chromosome 7, trisomy 7p", "chromosome 7p duplication", "7p partial trisomy syndrome", "7p partial trisomy (disorder)", "partial trisomy of chromosome 7p", "chromosome 7p duplication syndrome", "partial duplication of chromosome 7p", "7p partial trisomy syndrome (diagnosis)", "anomaly of chromosome pair 7 partial trisomy 7p", "partial trisomy of the short arm of chromosome 7", "partial duplication of the short arm of chromosome 7", "partial duplication of the short arm of chromosome type 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of the short arm of chromosome 7", "shortest_name_length": 10}
{"curie": "MONDO:0018253", "names": ["intellectual disability-facial dysmorphism-hand anomalies syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability-facial dysmorphism-hand anomalies syndrome", "shortest_name_length": 66}
{"curie": "UMLS:C1336418", "names": ["Stage IV Hepatocellular Cancer", "Stage IV Liver Cell Cancer AJCC v6", "Liver Cell Cancer Stage IV AJCC v6", "Stage IV Liver Cell Carcinoma AJCC v6", "Hepatocellular Cancer Stage IV AJCC v6", "Stage IV Hepatocellular Cancer AJCC v6", "Stage IV Hepatocellular Carcinoma AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Hepatocellular Carcinoma AJCC v6", "shortest_name_length": 30}
{"curie": "MONDO:0008427", "names": ["SCE, frequency of", "SCE, FREQUENCY OF", "SISTER CHROMATID EXCHANGE, FREQUENCY OF", "sister chromatid exchange, frequency of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sister chromatid exchange, frequency of", "shortest_name_length": 17}
{"curie": "MONDO:0013960", "names": ["SANDD", "Sinoatrial node dysfunction and deafness", "sinoatrial node dysfunction and deafness", "SINOATRIAL NODE DYSFUNCTION AND DEAFNESS", "Sinoatrial node dysfunction and hearing loss", "Sinoatrial node dysfunction and deafness (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sinoatrial node dysfunction and deafness", "shortest_name_length": 5}
{"curie": "MONDO:0000933", "names": ["subglottis tumor", "subglottic tumor", "Subglottic Tumor", "Subglottic tumor", "Subglottis Tumor", "subglottic neoplasm", "Subglottis Neoplasm", "tumor of subglottis", "subglottis neoplasm", "Subglottic Neoplasm", "Tumor of subglottis", "Tumor of Subglottis", "Tumour of subglottis", "neoplasm of subglottis", "Neoplasm of Subglottis", "Neoplasm of subglottis", "tumor of the subglottis", "Tumor of the Subglottis", "neoplasm of the subglottis", "Neoplasm of the Subglottis", "subglottis benign neoplasm", "laryngeal neoplasm subglottis", "subglottis neoplasm (disease)", "Neoplasm of subglottis (disorder)", "neoplasm of subglottis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subglottis neoplasm", "shortest_name_length": 16}
{"curie": "MONDO:0022990", "names": ["diphallus rachischisis imperforate anus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diphallus rachischisis imperforate anus", "shortest_name_length": 39}
{"curie": "MONDO:0005130", "names": ["Sprue", "sprue", "celiac", "sprues", "Thaysen", "Celiac Sprue", "celiac sprue", "CELIAC SPRUE", "Celiac sprue", "celiac sprues", "Sprue, Celiac", "Coeliac sprue", "CELIAC DISEASE", "Celiac Disease", "Celiac disease", "celiac disease", "coeliac disease", "Coeliac disease", "Disease, Celiac", "celiac diseases", "Celiac syndrome", "celiac syndrome", "Disease;coeliac", "coeliac syndrome", "Coeliac syndrome", "Nontropical Sprue", "CS - Celiac sprue", "Nontropical sprue", "nontropical sprue", "NONTROPICAL SPRUE", "nontropical; sprue", "Gluten enteropathy", "Non-tropical sprue", "non-tropical sprue", "sprue; nontropical", "gluten intolerance", "Sprue, Nontropical", "gluten enteropathy", "non tropical sprue", "CS - Coeliac sprue", "Non Tropical Sprue", "Gluten Enteropathy", "Enteropathy, Gluten", "CD - Celiac disease", "Gluten Enteropathies", "CD - Coeliac disease", "Enteropathies, Gluten", "Idiopathic steatorrhea", "idiopathic steatorrhea", "idiopathic; steatorrhea", "Idiopathic steatorrhoea", "Gluten-responsive sprue", "steatorrhea; idiopathic", "Celiac disease (disorder)", "Gluten-induced enteropathy", "gluten-induced enteropathy", "celiac disease (diagnosis)", "Gluten-Induced Enteropathy", "Wheat-sensitive enteropathy", "Gluten sensitive enteropathy", "gluten-sensitive enteropathy", "Gluten-sensitive enteropathy", "Gluten-Sensitive Enteropathy", "Gluten Sensitive Enteropathy", "gluten-sensitive; enteropathy", "celiac idiopathic steatorrhea", "Enteropathy, Gluten-Sensitive", "enteropathy; gluten-sensitive", "Gluten-Sensitive Enteropathies", "Enteropathies, Gluten-Sensitive", "GSE - Gluten-sensitive enteropathy", "Gluten-induced enteropathy syndrome", "celiac idiopathic steatorrhea (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "celiac disease", "shortest_name_length": 5}
{"curie": "MONDO:0002251", "names": ["cph", "CPH", "hepatitis", "HEPATITIS", "Hepatitis", "hepatitides", "Hepatitides", "Hepatitis NOS", "HEPATITIS NOS", "Hepatitis, NOS", "acute hepatitis", "animal hepatitis", "chronic hepatitis", "Liver inflammation", "liver inflammation", "liver; inflammation", "inflammation; liver", "HEPATITIS NONSPECIFIC", "HEPATITIS, UNRESOLVED", "unspecified hepatitis", "nonspecific hepatitis", "Hepatitis nonspecific", "inflammation of liver", "hepatitis (diagnosis)", "Nonspecific hepatitis", "Hepatitis, unspecified", "Inflammatory liver disease", "inflammatory liver disease", "Chronic persistent hepatitis", "chronic persistent hepatitis", "HEPATITIS CHRONIC PERSISTENT", "Chronic Persistent Hepatitis", "hepatitis chronic persistent", "Hepatitis chronic persistent", "liver; disease, inflammatory", "HEPATITIS, CHRONIC PERSISTENT", "Hepatitis, Chronic Persistent", "Inflammatory disease of liver", "acute/subac. necrosis of liver", "hepatitis; chronic, persistent", "Inflammatory disorder of liver", "Chronic Persistent Hepatitides", "acute and subacute liver necrosis", "Acute and subacute liver necrosis", "CPH - Chronic persistent hepatitis", "acute and subacute hepatic necrosis", "hepatic necrosis acute and subacute", "Acute and subacute necrosis of liver", "Inflammatory liver disease, unspecified", "Chronic persistent hepatitis (disorder)", "chronic persistent hepatitis (diagnosis)", "Inflammatory disease of liver (disorder)", "disease (or disorder); liver, inflammatory", "Acute and subacute liver necrosis (disorder)", "acute and subacute hepatic necrosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatitis", "shortest_name_length": 3}
{"curie": "UMLS:C4038730", "names": ["Asthma-COPD overlap syndrome", "Asthma COPD Overlap Syndrome", "Asthma-COPD Overlap Syndrome", "Asthma-COPD Overlap Syndromes", "Overlap Syndrome, Asthma-COPD", "Asthma-COPD overlap syndrome (ACOS)", "Asthma-chronic obstructive pulmonary disease overlap syndrome", "Asthma Chronic Obstructive Pulmonary Disease Overlap Syndrome", "Asthma-Chronic Obstructive Pulmonary Disease Overlap Syndrome", "asthma-chronic obstructive pulmonary disease overlap syndrome", "Asthma-chronic obstructive pulmonary disease overlap syndrome (disorder)", "asthma-chronic obstructive pulmonary disease overlap syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Asthma-Chronic Obstructive Pulmonary Disease Overlap Syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0043355", "names": ["Collagenous Gastritis", "collagenous gastritis", "Collagenous gastritis", "Collagenous gastritis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "collagenous gastritis", "shortest_name_length": 21}
{"curie": "UMLS:C5555193", "names": ["Platinum-Refractory Malignant Female Reproductive System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Platinum-Refractory Malignant Female Reproductive System Neoplasm", "shortest_name_length": 65}
{"curie": "UMLS:C3502051", "names": ["Thrombophilia, Hereditary, Due To Protein S Deficiency, Autosomal Recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thrombophilia, Hereditary, Due To Protein S Deficiency, Autosomal Recessive", "shortest_name_length": 75}
{"curie": "MONDO:0010491", "names": ["XLAG", "X-linked acrogigantism", "X-LINKED ACROGIGANTISM", "chromosome Xq26.3 DUPLICATION syndrome", "CHROMOSOME Xq26.3 DUPLICATION SYNDROME", "Chromosome Xq26 microduplication syndrome", "CHROMOSOME Xq26 MICRODUPLICATION SYNDROME", "chromosome Xq26 microduplication syndrome", "familial infantile gigantism due to dup(X)q(26)", "X-LAG (X-linked acrogigantism) due to dup(X)q(26)", "X-linked acrogigantism due to Xq26 microduplication", "familial infantile gigantism due to Xq26 microduplication", "chromosome xq26.3 duplication syndrome, X-linked dominant", "X-LAG (X-linked acrogigantism) due to Xq26 microduplication", "X-linked acrogigantism due to Xq26 microduplication (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked acrogigantism due to Xq26 microduplication", "shortest_name_length": 4}
{"curie": "UMLS:C5419059", "names": ["Advanced Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Diffuse Large B-Cell Lymphoma", "shortest_name_length": 38}
{"curie": "MONDO:0007771", "names": ["MUH", "FPHH", "Melanosis, Universal", "melanosis, universal", "melanosis universalis hereditaria", "hyperpigmentation, familial progressive, 2", "hyperpigmentation with or without hypopigmentation", "hyperpigmentation, familial progressive, 2, formerly", "macules, hereditary congenital hypopigmented and hyperpigmented", "familial progressive hyperpigmentation with or without hypopigmentation", "hyperpigmentation with or without hypopigmentation, familial progressive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperpigmentation with or without hypopigmentation, familial progressive", "shortest_name_length": 3}
{"curie": "MONDO:0004013", "names": ["Adult Sarcoma Botryoides of the Vagina", "adult vagina botryoid rhabdomyosarcoma", "adult sarcoma Botryoides of the vagina", "Adult Vaginal Embryonal Rhabdomyosarcoma", "adult vagina botryoid embryonal rhabdomyosarcoma", "Adult Vaginal Botryoid-Type Embryonal Rhabdomyosarcoma", "Adult Botryoid-Type Embryonal Rhabdomyosarcoma of the Vagina", "adult botryoid-type embryonal rhabdomyosarcoma of the vagina", "botryoid-type embryonal rhabdomyosarcoma of the vagina of adults"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult vagina botryoid embryonal rhabdomyosarcoma", "shortest_name_length": 38}
{"curie": "MONDO:0018506", "names": ["mesenchymal tumor of small bowel", "mesenchymal tumor of small intestine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mesenchymal tumor of small intestine", "shortest_name_length": 32}
{"curie": "MONDO:0008848", "names": ["Heart Block", "AV DISSOCIATION", "AV Dissociation", "AV dissociation", "A-V dissociation", "A V Dissociation", "Dissociation, AV", "A-V Dissociation", "A-V DISSOCIATION", "Dissociation, A-V", "A-V Dissociations", "Dissociations, A-V", "Isorhythmic dissociation", "interference dissociation", "Interference dissociation", "Dissociation, isorhythmic", "dissociation; interference", "interference; dissociation", "Dissociation, interference", "ATRIOVENTRICULAR DISSOCIATION", "Atrioventricular dissociation", "Atrioventricular Dissociation", "atrioventricular dissociation", "Dissociation, Atrioventricular", "Atrioventricular Dissociations", "Dissociation, atrioventricular", "Dissociations, Atrioventricular", "P and QRS complexes dissociated", "Dissociation auriculoventricular", "DISSOCIATION AURICULOVENTRICULAR", "Auriculo-Ventricular Dissociation", "Auriculo Ventricular Dissociation", "Auriculo-Ventricular Dissociations", "Dissociation, Auriculo-Ventricular", "Dissociations, Auriculo-Ventricular", "ATRIOVENTRICULAR DISSOCIATION, COMPLETE", "atrioventricular dissociation (disease)", "Atrioventricular dissociation (disorder)", "atrioventricular dissociation (diagnosis)", "Atrioventricular Dissociation by EKG Finding", "Atrioventricular Dissociation by ECG Finding", "auriculoventricular or atrioventricular; dissociation", "dissociation; auriculoventricular or atrioventricular"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrioventricular dissociation", "shortest_name_length": 11}
{"curie": "MONDO:0019829", "names": ["Congenital anomaly of the SVC", "congenital anomaly of the SVC", "Superior vena cava abnormality", "Superior caval vein abnormality", "SVC - Superior vena cava abnormality", "SCV - Superior caval vein abnormality", "congenital anomaly of superior vena cava", "Congenital anomaly of superior vena cava", "congenital anomaly of superior caval vein", "Congenital anomaly of superior caval vein", "Congenital anomaly of superior vena cava, NOS", "Congenital anomaly of superior vena cava (disorder)", "congenital anomaly of superior vena cava (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital anomaly of superior vena cava", "shortest_name_length": 29}
{"curie": "MONDO:0000845", "names": ["osteitis fibrosa", "fibrous dyplasia", "Osteitis fibrosa", "fibrosa osteitis", "Fibrous dyplasia", "fibrosa; osteitis", "fibrous dysplasia", "dysplasia fibrous", "Fibrous dysplasia", "osteitis; fibrosa", "FIBROUS DYSPLASIA", "Fibrous Dysplasia", "Dysplasia, fibrous", "Jaffe-Lichtenstein", "dysplasias fibrous", "Osteitis fibrosa, NOS", "fibrous dysplasia bone", "Bone Fibrous Dysplasia", "bone dysplasia fibrous", "Bone Fibrous Dysplasias", "bone; fibrous dysplasia", "bone; dysplasia, fibrous", "dysplasia; fibrous, bone", "fibrous; dysplasia, bone", "fibrous dysplasia of bone", "Fibrous dysplasia of bone", "Fibrous Dysplasia of Bone", "Jaffe Lichtenstein Disease", "Jaffe-Lichtenstein Disease", "Jaffe-Lichtenstein syndrome", "Osteitis fibrosa disseminata", "Osteitis Fibrosa Disseminata", "Fibrous dysplasia of the bones", "Fibrous dysplasia of bone, NOS", "Fibrous dysplasia of bone (disorder)", "Fibrous dysplasia of bone (diagnosis)", "Fibrous dysplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibrous dysplasia", "shortest_name_length": 16}
{"curie": "MONDO:0044212", "names": ["CSU", "CIU", "Chronic Idiopathic Urticaria", "chronic idiopathic urticaria", "Idiopathic Chronic Urticaria", "Chronic idiopathic urticaria", "Idiopathic Urticaria, Chronic", "Chronic Urticaria, Idiopathic", "Idiopathic Chronic Urticarias", "Chronic Spontaneous Urticaria", "Urticaria, Idiopathic Chronic", "Chronic Idiopathic Urticarias", "Urticaria, Chronic Idiopathic", "idiopathic urticaria, chronic", "Chronic spontaneous urticaria", "Urticaria, Chronic Spontaneous", "Chronic Spontaneous Urticarias", "Spontaneous Urticaria, Chronic", "CSU - chronic spontaneous urticaria", "Chronic idiopathic urticaria (disorder)", "chronic idiopathic urticaria (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic idiopathic urticaria", "shortest_name_length": 3}
{"curie": "UMLS:C4521639", "names": ["Stage II Esophageal Adenocarcinoma", "Clinical Stage II Esophageal Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage II Esophageal Adenocarcinoma AJCC v8", "shortest_name_length": 34}
{"curie": "UMLS:C0855142", "names": ["Stage I Nodal Marginal Zone Lymphoma", "Nodal marginal zone B-cell lymphoma stage I", "Stage I Nodal Marginal Zone B-Cell Lymphoma", "Nodal Marginal Zone B-Cell Lymphoma Stage I", "Ann Arbor Stage I Nodal Marginal Zone Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nodal marginal zone B-cell lymphoma stage I", "shortest_name_length": 36}
{"curie": "UMLS:C0267358", "names": ["Duodenal fistula", "Duodenal Fistula", "duodenal fistula", "duodenal fistulas", "fistula; duodenum", "duodenum; fistula", "DF - Duodenal fistula", "Duodenal fistula, NOS", "Duodenal fistula (disorder)", "small bowel fistula duodenum", "Duodenal fistula (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Duodenal fistula", "shortest_name_length": 16}
{"curie": "UMLS:C0235832", "names": ["HERNIA CONGENITAL", "Congenital hernia", "Hernia congenital", "congenital hernia", "congenital hernias", "Congenital hernia NOS", "CONGENITAL PROTRUSIONS", "Congenital hernia, NOS", "Congenital protrusion, NOS", "Congenital herniation, NOS", "Congenital evagination, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital hernia", "shortest_name_length": 17}
{"curie": "MONDO:0029136", "names": ["LGMDR23", "muscular dystrophy, limb-girdle, autosomal recessive 23", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23", "laminin subunit alpha 2-related limb-girdle muscular dystrophy R23"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy, limb-girdle, autosomal recessive 23", "shortest_name_length": 7}
{"curie": "MONDO:0008681", "names": ["WAGR", "AGR triad", "11p monosomy", "monosomy 11p", "WAGR Complex", "deletion 11p", "Del(11)(p13)", "11p deletion", "WAGR syndrome", "WAGR SYNDROME", "WAGR Syndrome", "Wagr Syndrome", "Complex, WAGR", "deletion 11p13", "Deletion 11p13", "monosomy 11p13", "Syndrome, WAGR", "WAGR Syndromes", "Monosomy 11p13", "WAGR Complices", "partial monosomy 11p", "11p deletion syndrome", "chromosome 11p deletion", "WAGR 11p13 deletion syndrome", "11p Partial Monosomy Syndrome", "WAGR Contiguous Gene Syndrome", "11p partial monosomy syndrome", "Contiguous Gene Syndrome, WAGR", "Aniridia-Wilms tumor association", "chromosome 11p deletion syndrome", "Aniridia-Wilms tumour association", "chromosome 11P13 deletion syndrome", "chromosome 11p13 deletion syndrome", "Chromosome 11p13 Deletion Syndrome", "Chromosome 11p13 deletion syndrome", "CHROMOSOME 11p13 DELETION SYNDROME", "11p partial monosomy syndrome (disorder)", "11p partial monosomy syndrome (diagnosis)", "Chromosome 11p13 deletion syndrome (disorder)", "Wilms Tumor-Aniridia-Genitourinary Anomalies-MR Syndrome", "anomaly of chromosome pair 11p partial monosomy syndrome", "Wilms Tumor-Aniridia-Genital Anomalies-Retardation Syndrome", "Wilms tumor-aniridia-gonadoblastoma-mental retardation syndrome", "Wilms Tumor-Aniridia-Gonadoblastoma-Mental Retardation Syndrome", "Wilms tumor-aniridia-gonadoblastoma-intellectual disability syndrome", "Wilms Tumor-Aniridia-Genitourinary Anomalies-Mental Retardation Syndrome", "Wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome", "Wilms tumor-Aniridia-Genitourinary Anomalies-Mental Retardation syndrome", "Wilms tumor, aniridia, genitourinary anomalies, mental retardation syndrome", "Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation Syndrome", "Wilms tumor-aniridia-genitourinary anomalies-intellectual disability syndrome", "Wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome", "Wilms Tumor, Aniridia, Genitourinary Anomalies and Developmental Delay Syndrome", "Wilms tumor, aniridia, genitourinary anomalies, and mental retardation syndrome", "Wilms tumour, aniridia, genitourinary anomalies and mental retardation syndrome", "Wilms tumor, aniridia, genitourinary anomalies and developmental delay syndrome", "WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATION SYNDROME", "Wilms Tumor, Aniridia, Genitourinary Anomalies, And Mental Retardation Syndrome", "Wilms tumor, aniridia, genitourinary anomalies, intellectual disability syndrome", "Wilms tumor, aniridia, genitourinary anomalies, and intellectual disability syndrome", "WAGR (Wilms tumor, aniridia, genitourinary anomalies and mental retardation) syndrome", "WAGR (Wilms tumour, aniridia, genitourinary anomalies and mental retardation) syndrome", "WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME", "Wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome, autosomal dominant, somatic mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "WAGR syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0016128", "names": ["Parasitic myositis", "parasitic myositis", "Parasitic myositis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parasitic myositis", "shortest_name_length": 18}
{"curie": "UMLS:C0520731", "names": ["nystagmus retraction", "Retraction nystagmus", "Retraction Nystagmus", "Nystagmus, Retraction", "Nystagmus retractorius", "Retraction nystagmus (disorder)", "Retraction nystagmus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retraction Nystagmus", "shortest_name_length": 20}
{"curie": "UMLS:C4520757", "names": ["Stage II Larynx Epidermoid Carcinoma", "Stage II Laryngeal Epidermoid Carcinoma", "Stage II Epidermoid Carcinoma of Larynx", "Stage II Larynx Squamous Cell Carcinoma", "Stage II Squamous Cell Carcinoma of Larynx", "Stage II Laryngeal Squamous Cell Carcinoma", "Stage II Epidermoid Carcinoma of the Larynx", "Stage II Laryngeal Throat Squamous Cell Cancer", "Stage II Squamous Cell Carcinoma of the Larynx", "Stage II Laryngeal Squamous Cell Carcinoma AJCC v6", "Stage II Laryngeal Squamous Cell Carcinoma AJCC v7", "Stage II Laryngeal Squamous Cell Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Laryngeal Squamous Cell Carcinoma AJCC v6 and v7", "shortest_name_length": 36}
{"curie": "MONDO:0010393", "names": ["MRX93", "XLID93", "X-linked mental retardation 93", "mental retardation, X-linked 93", "Mental Retardation, X-Linked 93", "MENTAL RETARDATION, X-LINKED 93", "intellectual disability, X-linked 93", "mental retardation, X-linked type 93", "intellectual disability, X-linked type 93", "X-linked mental retardation with macrocephaly", "Mental Retardation, X-Linked, With Macrocephaly", "mental retardation, X-linked, with macrocephaly", "MENTAL RETARDATION, X-LINKED, WITH MACROCEPHALY", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 93", "non-syndromic X-linked intellectual disability 93", "intellectual disability, X-linked, with macrocephaly", "BRWD3 non-syndromic X-linked intellectual disability", "intellectual developmental disorder, X-linked 93, X-linked recessive", "non-syndromic X-linked intellectual disability caused by mutation in BRWD3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 93", "shortest_name_length": 5}
{"curie": "UMLS:C5420153", "names": ["Advanced Thyroid Gland Anaplastic Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Thyroid Gland Anaplastic Carcinoma", "shortest_name_length": 43}
{"curie": "UMLS:C0750990", "names": ["Internal carotid artery thrombosis", "Thrombosis internal carotid artery", "Internal Carotid Artery Thrombosis", "Thrombosis, Internal Carotid Artery", "Thrombosis of internal carotid artery", "Thrombosis of internal carotid artery (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Internal Carotid Artery Thrombosis", "shortest_name_length": 34}
{"curie": "MONDO:0004725", "names": ["Rectal cancer stage 0", "stage 0 rectal cancer", "stage 0 rectum cancer", "Stage 0 Rectal Cancer", "rectal cancer, stage 0", "rectum cancer, stage 0", "Severe Rectal Dysplasia", "marked rectal dysplasia", "severe rectal dysplasia", "Marked Rectal Dysplasia", "rectum in situ carcinoma", "rectal carcinoma in situ", "Rectal carcinoma in situ", "rectum carcinoma in situ", "Rectal Carcinoma in situ", "stage 0 rectal carcinoma", "Stage 0 Rectal Carcinoma", "Rectal carcinoma stage 0", "stage 0 rectum carcinoma", "Cancer in situ of rectum", "Severe dysplasia of rectum", "marked dysplasia of rectum", "Marked Dysplasia of Rectum", "severe dysplasia of rectum", "Severe Dysplasia of Rectum", "Carcinoma in situ of rectum", "stage 0 carcinoma of rectum", "Carcinoma in situ of Rectum", "Stage 0 Carcinoma of Rectum", "carcinoma in situ of rectum", "Stage 0 Rectal Cancer AJCC v7", "stage 0 rectal cancer aJCC v6", "stage 0 rectal cancer aJCC v7", "Stage 0 Rectal Cancer AJCC v6", "severe dysplasia of the rectum", "marked dysplasia of the rectum", "Severe Dysplasia of the Rectum", "Marked Dysplasia of the Rectum", "stage 0 carcinoma of the rectum", "Stage 0 Carcinoma of the Rectum", "Carcinoma in situ of the Rectum", "carcinoma in situ of the rectum", "rectal neoplasm carcinoma in situ", "stage 0 rectal cancer aJCC v6 and v7", "Stage 0 Rectal Cancer AJCC v6 and v7", "Severe dysplasia of rectum (disorder)", "Carcinoma in situ of rectum (disorder)", "carcinoma in situ of rectum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rectum carcinoma in situ", "shortest_name_length": 21}
{"curie": "MONDO:0012170", "names": ["DFNB36", "autosomal recessive deafness 36", "deafness, autosomal recessive 36", "Deafness, Autosomal Recessive 36", "autosomal recessive nonsyndromic deafness 36", "ESPN autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 36", "autosomal recessive nonsyndromic deafness type 36", "DEAFNESS, AUTOSOMAL DOMINANT, WITHOUT VESTIBULAR INVOLVEMENT", "deafness, autosomal dominant, without vestibular involvement", "autosomal recessive nonsyndromic deafness caused by mutation in ESPN", "DEAFNESS, AUTOSOMAL RECESSIVE 36, WITH OR WITHOUT VESTIBULAR INVOLVEMENT", "deafness, autosomal recessive 36, with or without vestibular involvement", "deafness, neurosensory, without vestibular involvement, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 36", "shortest_name_length": 6}
{"curie": "MONDO:0000453", "names": ["SQTS", "Short QT Syndrome", "Short Qt Syndrome", "SHORT QT SYNDROME", "short QT syndrome", "Short QT syndrome", "Genetic short QT syndrome", "familial short QT syndrome", "Familial short QT syndrome", "Short QT syndrome (disorder)", "short QT syndrome (diagnosis)", "ventricular arrhythmia associated with short QT syndrome", "Ventricular arrhythmia associated with short QT syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short QT syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C4520856", "names": ["stage III endometrial cancer", "stage III cancer of the uterus", "Stage III Endometrial Cancer AJCC v6", "Stage III Uterine Corpus Cancer AJCC v6", "Stage III Cancer of Uterine Corpus AJCC v6", "Stage III Cancer of the Corpus Uteri AJCC v6", "Stage III Cancer of the Uterine Corpus AJCC v6", "Stage III Uterine (including Endometrial) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Uterine Corpus Cancer AJCC v6", "shortest_name_length": 28}
{"curie": "MONDO:0017738", "names": ["lysosomal glycogen storage disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lysosomal glycogen storage disease", "shortest_name_length": 34}
{"curie": "MONDO:0007301", "names": ["CCMS", "CCM Syndrome", "CCM syndrome", "rib-gap syndrome", "cerebrocostomandibular syndrome", "Cerebrocostomandibular syndrome", "CEREBROCOSTOMANDIBULAR SYNDROME", "CEREBROCOSTOMANDIBULAR syndrome", "Cerebrocostomandibular Syndrome", "rib gap defects with micrognathia", "Cerebro-costo-mandibular syndrome", "Rib gap defects with micrognathia", "rib Gap defects with micrognathia", "RIB GAP DEFECTS WITH MICROGNATHIA", "cerebro-costo-mandibular syndrome", "Rib Gap Defects with Micrognathia", "Smith-Theiler-Schachenmann syndrome", "rib gap defect-micrognathia syndrome", "cerebrocostomandibular (CCM) syndrome (CCMS)", "Cerebro-costo-mandibular syndrome (disorder)", "cerebro-costo-mandibular syndrome (diagnosis)", "congenital deformity of head cerebro-costo-mandibular syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebrocostomandibular syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C4683621", "names": ["Chronic Lymphocytic Leukemia- Binet Staging System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic Lymphocytic Leukemia- Binet Staging System", "shortest_name_length": 50}
{"curie": "UMLS:C2981703", "names": ["Stage IIIB Eyelid Carcinoma", "stage IIIB eyelid carcinoma", "Stage IIIB Eyelid Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Eyelid Carcinoma AJCC v7", "shortest_name_length": 27}
{"curie": "UMLS:C5444182", "names": ["Breast Intracystic Papillary Carcinoma", "Encapsulated Breast Papillary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Encapsulated Breast Papillary Carcinoma", "shortest_name_length": 38}
{"curie": "MONDO:0010736", "names": ["SHFD2", "SHSF2", "SHFM2", "Split-Hand-Foot Deformity 2", "split-hand/foot deformity 2", "SPLIT-HAND/FOOT DEFORMITY 2", "split hand foot deformity 2", "split hand-foot malformation 2", "split-hand/foot malformation 2", "Split-Hand-Foot Malformation 2", "split hand/foot malformation 2", "Split-Hand Foot Malformation 2", "SPLIT-HAND/FOOT MALFORMATION 2", "Split hand foot anomaly - X-linked", "split hand foot anomaly - X-linked", "split hand-foot malformation type 2", "split hand/foot malformation X-linked", "Split hand-foot malformation X-linked", "split-hand/split-foot anomaly, X-linked", "Split-Hand-Split-Foot Anomaly, X-Linked", "SPLIT-HAND/SPLIT-FOOT ANOMALY, X-LINKED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "split hand-foot malformation 2", "shortest_name_length": 5}
{"curie": "MONDO:0010521", "names": ["AIH1", "AI1E", "enamel hypoplasia X-linked", "X-linked enamel hypoplasia", "ENAMEL HYPOPLASIA, X-LINKED", "enamel hypoplasia, X-linked", "AMELX amelogenesis imperfecta", "amelogenesis imperfecta type 1E", "amelogenesis imperfecta type IE", "amelogenesis imperfecta, type IE", "amelogenesis imperfecta, type 1E", "AMELOGENESIS IMPERFECTA, TYPE IE", "X-linked amelogenesis imperfecta 1", "amelogenesis imperfecta X-linked 1", "amelogenesis imperfecta, X-linked 1", "AMELOGENESIS IMPERFECTA, X-LINKED 1", "Amelogenesis imperfecta, X-linked 1", "amelogenesis imperfecta, type 1E, X-linked dominant", "amelogenesis imperfecta caused by mutation in AMELX", "amelogenesis imperfecta hypoplastic/hypomaturation X-linked 1", "X-linked amelogenesis imperfecta hypoplastic/hypomaturation 1", "amelogenesis imperfecta, hypoplastic/hypomaturation, X-linked 1", "AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 1", "Amelogenesis imperfecta, hypoplastic-hypomaturation, X-linked 1", "amelogenesis imperfecta hypomaturationtype with snow-capped teeth", "AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, WITH SNOW-CAPPED TEETH", "amelogenesis imperfecta, hypomaturation type, with Snow-capped teeth", "Amelogenesis Imperfecta, Hypomaturation Type, with Snow-Capped Teeth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amelogenesis imperfecta type 1E", "shortest_name_length": 4}
{"curie": "MONDO:0013981", "names": ["FCM", "MYOCL1", "familial myoclonus", "myoclonus, familial", "MYOCLONUS, FAMILIAL, 1", "Familial cortical myoclonus", "familial cortical myoclonus", "MYOCLONUS, FAMILIAL CORTICAL", "myoclonus, familial cortical", "Familial myoclonus of cerebral cortex", "Familial myoclonus of cerebral cortex (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myoclonus, familial", "shortest_name_length": 3}
{"curie": "UMLS:C0151734", "names": ["injection site inflammation", "INFLAMMATION INJECTION SITE", "INJECTION SITE INFLAMMATION", "Inflammation injection site", "Injection site inflammation", "Inflammation at site of injection", "Injection site inflammation (disorder)", "injection site inflammation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site inflammation", "shortest_name_length": 27}
{"curie": "MONDO:0006919", "names": ["K+ decreased", "k deficiency", "K deficiency", "deficiency k", "potassium deficiency", "Potassium deficiency", "POTASSIUM DEFICIENCY", "Potassium Deficiency", "deficiency potassium", "deficiency; potassium", "potassium; deficiency", "Deficiency, Potassium", "potassium deficiencies", "Potassium Deficiencies", "Deficiencies, Potassium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "potassium deficiency", "shortest_name_length": 12}
{"curie": "MONDO:0003329", "names": ["ureter; occlusion", "occlusion; ureter", "ureter obstruction", "Obstruction;ureter", "Ureter Obstruction", "OBSTRUCTION URETER", "Ureter obstruction", "URETER OBSTRUCTION", "Obstruction ureter", "obstruction ureter", "obstruction; ureter", "URETER, OBSTRUCTION", "occlusion of ureter", "ureter; obstruction", "Occlusion of ureter", "Ureteric obstruction", "Ureteral obstruction", "ureteral obstruction", "ureteric obstruction", "Ureteral Obstruction", "obstructions ureters", "Obstruction of ureter", "obstruction of ureter", "Obstruction, Ureteral", "Ureters--Obstructions", "Ureteral Obstructions", "Obstructions, Ureteral", "Occlusion NOS of ureter", "Occlusion of ureter NOS", "Occlusion of ureter, NOS", "Ureteric obstruction, NOS", "Other ureteric obstruction", "ureteral obstruction (disease)", "Occlusion of ureter (disorder)", "occlusion of ureter (diagnosis)", "Obstruction of ureter (disorder)", "obstruction of ureter (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ureteral obstruction", "shortest_name_length": 17}
{"curie": "UMLS:C1514838", "names": ["Renal Cell Carcinoma Associated with t(X;1)(p11.2;p34)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal Cell Carcinoma Associated with t(X;1)(p11.2;p34)", "shortest_name_length": 54}
{"curie": "UMLS:C0877104", "names": ["Retinal toxicity", "retinal toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retinal toxicity", "shortest_name_length": 16}
{"curie": "UMLS:C4552928", "names": ["Stage IC Fallopian Tube Cancer", "Stage IC Fallopian Tube Cancer AJCC v8", "Stage IC Fallopian Tube Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IC Fallopian Tube Cancer AJCC v8", "shortest_name_length": 30}
{"curie": "UMLS:C5420766", "names": ["Benign Epithelial Melanoses of the Conjunctiva"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Epithelial Melanoses of the Conjunctiva", "shortest_name_length": 46}
{"curie": "MONDO:0016857", "names": ["blepharophimosis-epicanthus inversus-ptosis due to 3q23 rearrangement syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blepharophimosis-epicanthus inversus-ptosis due to 3q23 rearrangement syndrome", "shortest_name_length": 78}
{"curie": "UMLS:C5554612", "names": ["Thoracic Chordoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thoracic Chordoma", "shortest_name_length": 17}
{"curie": "UMLS:C0042505", "names": ["Ventral Hernia without Mention of Obstruction or Gangrene", "Ventral hernia without mention of obstruction or gangrene"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ventral hernia without mention of obstruction or gangrene", "shortest_name_length": 57}
{"curie": "UMLS:C0334536", "names": ["benign; angioendothelioma", "angioendothelioma; benign", "Benign hemangioendothelioma", "Benign Hemangioendothelioma", "Hemangioendothelioma, benign", "Haemangioendothelioma benign", "benign; hemangioendothelioma", "hemangioendothelioma; benign", "Benign haemangioendothelioma", "Haemangioendothelioma, benign", "Hemangioendothelioma, benign (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemangioendothelioma, benign", "shortest_name_length": 25}
{"curie": "UMLS:C0456013", "names": ["Acrocyanosis neonatal", "acrocyanosis; newborn", "newborn; acrocyanosis", "Neonatal Acrocyanosis", "Neonatal acrocyanosis", "Perinatal acrocyanosis", "Neonatal acrocyanosis (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neonatal acrocyanosis", "shortest_name_length": 21}
{"curie": "UMLS:C4054941", "names": ["FSH Receptor Deficiency", "Follicle Stimulating Hormone Receptor Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Follicle Stimulating Hormone Receptor Deficiency", "shortest_name_length": 23}
{"curie": "MONDO:0016772", "names": ["annular LP", "Annular LP", "LICHEN ANNULARIS", "Annular lichen planus", "annular lichen planus", "Lichen planus annularis", "planus; lichen, annularis", "lichen; planus, annularis", "Annular lichen planus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "annular lichen planus", "shortest_name_length": 10}
{"curie": "MONDO:0014043", "names": ["MCPH10", "primary autosomal recessive microcephaly 10", "Microcephalic primordial dwarfism Walsh type", "Microcephalic primordial dwarfism, Walsh type", "MICROCEPHALY 10, PRIMARY, AUTOSOMAL RECESSIVE", "microcephaly 10, primary, autosomal recessive", "microcephalic primordial dwarfism, Walsh type", "Microcephalic primordial dwarfism due to ZNF335 deficiency", "microcephalic primordial dwarfism due to ZNF335 deficiency", "Microcephalic primordial dwarfism due to zinc finger protein 335 deficiency", "Microcephalic primordial dwarfism due to ZNF335 (zinc finger protein 335) deficiency", "Microcephalic primordial dwarfism due to zinc finger protein 335 deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephalic primordial dwarfism due to ZNF335 deficiency", "shortest_name_length": 6}
{"curie": "MONDO:0005608", "names": ["varicella zoster infection", "infection varicella zoster", "Varicella Zoster infection", "VARICELLA ZOSTER INFECTION", "Varicella zoster infection", "Varicella Zoster Infection", "infections varicella zoster", "Varicella-zoster virus infection", "Varicella zoster virus infection", "varicella-zoster virus infection", "Varicella-zoster Virus infection", "Varicella-Zoster Virus Infection", "Varicella Zoster Virus Infection", "Varicella-zoster virus infection (disorder)", "varicella-zoster virus infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "varicella zoster infection", "shortest_name_length": 26}
{"curie": "UMLS:C4727596", "names": ["Metastatic Urethral Carcinoma", "Metastatic Carcinoma of Urethra", "Metastatic Carcinoma of the Urethra"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Urethral Carcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0043079", "names": ["acute rheumatism", "acute rheumatic arthritis", "acute articular rheumatism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute articular rheumatism", "shortest_name_length": 16}
{"curie": "MONDO:0021035", "names": ["APMR", "APMR1", "AMR Syndrome", "AMR SYNDROME", "ALOPECIA-MENTAL RETARDATION SYNDROME 1", "Alopecia-Mental Retardation Syndrome 1", "alopecia-mental retardation syndrome 1", "ALOPECIA-INTELLECTUAL DISABILITY SYNDROME 1", "alopecia-intellectual disability syndrome 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alopecia-intellectual disability syndrome 1", "shortest_name_length": 4}
{"curie": "MONDO:0021662", "names": ["Bile Duct Tumor", "bile duct tumor", "bile duct neoplasm", "tumor of bile duct", "Bile Duct Neoplasm", "Neoplasm, Bile Duct", "Bile Duct Neoplasms", "Neoplasms, Bile Duct", "neoplasm of bile duct", "bile duct neoplasm (disease)", "neoplasm of bile duct (diagnosis)", "intrahepatic and extrahepatic bile duct tumor", "Intrahepatic and Extrahepatic Bile Duct Tumor", "intrahepatic and extrahepatic bile duct neoplasm", "Intrahepatic and Extrahepatic Bile Duct Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bile duct neoplasm", "shortest_name_length": 15}
{"curie": "MONDO:0019929", "names": ["49,XXXXY", "XXXXY syndrome", "XXXXY; syndrome", "syndrome; XXXXY", "XXXXY aneuploidy", "49,XXXXY syndrome", "49,XXXXY Syndrome", "Klinefelter variant", "XXXXY syndrome (disorder)", "chromosome XXXXY syndrome", "49,XXXXY chromosomal anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "49,XXXXY syndrome", "shortest_name_length": 8}
{"curie": "UMLS:C4763745", "names": ["Other and Unspecified Infectious and Parasitic Diseases and their Sequelae"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Other and Unspecified Infectious and Parasitic Diseases and their Sequelae", "shortest_name_length": 74}
{"curie": "UMLS:C4087177", "names": ["Device related thrombosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Device related thrombosis", "shortest_name_length": 25}
{"curie": "UMLS:C5446446", "names": ["Lacrimal Drainage System Adenocarcinoma", "Adenocarcinoma of the Lacrimal Drainage System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lacrimal Drainage System Adenocarcinoma", "shortest_name_length": 39}
{"curie": "MONDO:0018679", "names": ["primary cutaneous plasmacytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary cutaneous plasmacytosis", "shortest_name_length": 31}
{"curie": "MONDO:0007671", "names": ["GFND", "GFND2", "GFND1", "Fibronectin glomerulopathy", "fibronectin glomerulopathy", "FIBRONECTIN GLOMERULOPATHY", "lobular glomerulopathy, familial", "LOBULAR GLOMERULOPATHY, FAMILIAL", "Lobular Glomerulopathy, Familial", "Fibronectin glomerulopathy (disorder)", "fibronectin glomerulopathy (diagnosis)", "glomerulopathy with fibronectin deposits", "Glomerulopathy with fibronectin deposits", "glomerulopathy with fibronectin deposits 1", "GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 1", "Glomerulopathy with fibronectin deposits 1", "glomerulopathy with fibronectin deposits 2", "Glomerulopathy with Fibronectin Deposits 1", "glomerulopathy with giant fibrillar deposits", "GLOMERULOPATHY WITH GIANT FIBRILLAR DEPOSITS", "Glomerulopathy with giant fibrillar deposits", "Glomerulopathy with Giant Fibrillar Deposits", "Glomerulopathy with giant fibrillar deposits (disorder)", "glomerulopathy with giant fibrillar deposits (diagnosis)", "glomerular nephritis, familial, with fibronectin deposits", "GLOMERULAR NEPHRITIS, FAMILIAL, WITH FIBRONECTIN DEPOSITS", "Glomerular nephritis, familial, with fibronectin deposits"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibronectin glomerulopathy", "shortest_name_length": 4}
{"curie": "UMLS:C5420275", "names": ["Oropharyngeal Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oropharyngeal Non-Hodgkin Lymphoma", "shortest_name_length": 34}
{"curie": "MONDO:0016109", "names": ["autosomal recessive distal myopathy", "distal myopathy, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive distal myopathy", "shortest_name_length": 35}
{"curie": "UMLS:C0742608", "names": ["Colon HP", "Colon MP", "Metaplastic Colon Polyp", "Colon Metaplastic Polyp", "Colon Hyperplastic Polyp", "Metaplastic Colonic Polyp", "colon hyperplastic polyps", "Colonic Hyperplastic Polyp", "Hyperplastic Colonic Polyp", "Metaplastic Polyp of Colon", "Hyperplastic Polyp of Colon", "COLON NOS POLYP HYPERPLASTIC", "Metaplastic Polyp of the Colon", "Hyperplastic Polyp of the Colon", "colon (non-specific) polyp hyperplastic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colon Hyperplastic Polyp", "shortest_name_length": 8}
{"curie": "MONDO:0004078", "names": ["Mucinous Intrahepatic Cholangiocarcinoma", "mucinous intrahepatic cholangiocarcinoma", "Mucin-Producing Intrahepatic Cholangiocarcinoma", "mucin-producing intrahepatic cholangiocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucinous intrahepatic cholangiocarcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0014139", "names": ["EDSP2", "EDSSPD2", "spEDS-B3GALT6", "EDSP2, FORMERLY", "B3GALT6-related spEDS", "Beta3GalT6-deficient EDS", "B3GALT6-related spondylodysplastic EDS", "Ehlers-Danlos syndrome progeroid type 2", "Ehlers-Danlos syndrome, progeroid type, 2", "B3GALT6 Ehlers-Danlos syndrome progeroid type", "EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 2", "Ehlers-Danlos syndrome, spondylodysplastic type, 2", "EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 2, FORMERLY", "Ehlers-Danlos syndrome, progeroid type, 2, formerly", "B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome", "Ehlers-Danlos syndrome progeroid type caused by mutation in B3GALT6", "Beta-1,3-galactosyltransferase 6-related spondylodysplastic Ehlers-Danlos syndrome", "Beta-1,3-galactosyltransferase 6-related spondylodysplastic Ehlers-Danlos syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ehlers-Danlos syndrome, spondylodysplastic type, 2", "shortest_name_length": 5}
{"curie": "UMLS:C4551574", "names": ["Stage 0", "stage 0 cancer of testis", "Stage 0 Cancer of Testis", "stage 0 testicular cancer", "Stage 0 Testicular Cancer", "stage 0 cancer of the testis", "Stage 0 Cancer of the Testis", "stage 0 testicular cancer AJCC v6", "Stage 0 Testicular Cancer AJCC v6", "Stage 0 Testicular Cancer AJCC v7", "stage 0 testicular cancer AJCC v7", "stage 0 testicular germ cell tumor", "stage 0 testicular carcinoma in situ", "Stage 0 Testicular Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Testicular Cancer AJCC v6 and v7", "shortest_name_length": 7}
{"curie": "UMLS:C0281331", "names": ["Pineocytoma", "Adult Pineocytoma", "adult pineocytoma", "pineocytoma, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Pineocytoma", "shortest_name_length": 11}
{"curie": "UMLS:C4521643", "names": ["Stage IV Esophageal Adenocarcinoma", "Clinical Stage IV Esophageal Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage IV Esophageal Adenocarcinoma AJCC v8", "shortest_name_length": 34}
{"curie": "MONDO:0021488", "names": ["Benign Lacrimal Gland Tumor", "benign lacrimal gland tumor", "benign tumor of lacrimal gland", "Benign Tumor of Lacrimal Gland", "benign lacrimal gland neoplasm", "lacrimal gland benign neoplasm", "Benign tumor of lacrimal gland", "Benign Lacrimal Gland Neoplasm", "Benign tumour of lacrimal gland", "benign neoplasm of lacrimal gland", "Benign neoplasm of lacrimal gland", "Benign Neoplasm of Lacrimal Gland", "benign tumor of the lacrimal gland", "Benign Tumor of the Lacrimal Gland", "benign neoplasm of the lacrimal gland", "Benign Neoplasm of the Lacrimal Gland", "Benign neoplasm of lacrimal gland (disorder)", "benign neoplasm of lacrimal gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of lacrimal gland", "shortest_name_length": 27}
{"curie": "MONDO:0004035", "names": ["Glomangiomatosis", "glomangiomatosis", "Glomangiomatosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glomangiomatosis", "shortest_name_length": 16}
{"curie": "MONDO:0014136", "names": ["PPH4", "PULMONARY HYPERTENSION, PRIMARY, 4", "pulmonary hypertension, primary, 4", "KCNK3 primary pulmonary hypertension", "pulmonary hypertension, primary, type 4", "primary pulmonary hypertension caused by mutation in KCNK3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary hypertension, primary, 4", "shortest_name_length": 4}
{"curie": "UMLS:C3272831", "names": ["Colorectal Sarcoma", "Large Intestinal Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Sarcoma", "shortest_name_length": 18}
{"curie": "UMLS:C1518190", "names": ["Malignant Lymphoma, Non-Cleaved Cell Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Lymphoma, Non-Cleaved Cell Type", "shortest_name_length": 41}
{"curie": "MONDO:0018172", "names": ["Malignant ovarian SCST", "malignant ovarian SCST", "Malignant Ovarian Sex Cord-Stromal Tumor", "malignant ovarian Sex cord-stromal tumor", "malignant ovarian sex cord-stromal tumor", "Malignant ovarian sex cord-stromal tumor", "malignant Sex cord-stromal tumor of ovary", "Malignant Sex Cord-Stromal Tumor of Ovary", "malignant sex cord stromal tumor of ovary", "Malignant sex cord stromal tumor of ovary", "ovarian sex cord-stromal tumor, malignant", "Malignant Ovarian Sex Cord-Stromal Neoplasm", "malignant ovarian Sex cord-stromal neoplasm", "malignant Sex cord-stromal tumor of the ovary", "Malignant Sex Cord-Stromal Tumor of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant sex cord stromal tumor of ovary", "shortest_name_length": 22}
{"curie": "MONDO:0022513", "names": ["Pasini and Pierini", "Atrophoderma of Pasini Pierini", "atrophoderma of pasini pierini", "atrophoderma of pierini pasini", "Pasini and Pierini; atrophoderma", "atrophoderma; Pasini and Pierini", "Atrophoderma of Pasini and Pierini", "atrophoderma of Pierini and Pasini", "congenital atrophoderma of Pasini and Pierini", "idiopathic atrophoderma of Pasini and Pierini", "Idiopathic atrophoderma of Pasini and Pierini", "Atrophoderma of Pasini and Pierini (diagnosis)", "Idiopathic atrophoderma of Pasini and Pierini (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrophoderma of Pierini and Pasini", "shortest_name_length": 18}
{"curie": "MONDO:0012178", "names": ["Mental Retardation with Optic Atrophy, Facial Dysmorphism, Microcephaly, and Short Stature", "mental retardation with optic atrophy, facial dysmorphism, microcephaly, and short stature", "MENTAL RETARDATION WITH OPTIC ATROPHY, FACIAL DYSMORPHISM, MICROCEPHALY, AND SHORT STATURE", "intellectual disability with optic atrophy, facial dysmorphism, microcephaly, and short stature"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability with optic atrophy, facial dysmorphism, microcephaly, and short stature", "shortest_name_length": 90}
{"curie": "MONDO:0020989", "names": ["Hb F disease", "HEMOGLOBIN F DIS", "hemoglobin; fetal", "fetal; hemoglobin", "Hemoglobin F Disease", "Disease, Hemoglobin F", "persistent; hemoglobin", "hemoglobin; persistent", "HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN", "Hereditary Persistence of Fetal Hemoglobin", "Hereditary persistence of fetal hemoglobin", "HEREDITARY PERSISTENCE of FETAL HEMOGLOBIN", "hereditary persistence of fetal hemoglobin", "Hereditary persistence of fetal haemoglobin", "Hereditary persistence of foetal haemoglobin", "Hereditary persistence of fetal hemoglobin [HPFH]", "HPFH - Hereditary persistence of fetal hemoglobin", "HPFH (hereditary persistence of fetal hemoglobin)", "Hereditary persistence of fetal haemoglobin [HPFH]", "HPFH - Hereditary persistence of fetal haemoglobin", "HPFH - Hereditary persistence of foetal haemoglobin", "Hereditary persistence of fetal hemoglobin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary persistence of fetal hemoglobin", "shortest_name_length": 12}
{"curie": "MONDO:0018738", "names": ["benign metanephric tumour"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign metanephric tumour", "shortest_name_length": 25}
{"curie": "MONDO:0022586", "names": ["bone dysplasia Moore type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bone dysplasia Moore type", "shortest_name_length": 25}
{"curie": "MONDO:0013206", "names": ["FECD6", "ZEB1 Fuchs' endothelial dystrophy", "corneal dystrophy, Fuchs endothelial, 6", "CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 6", "Corneal Dystrophy, Fuchs Endothelial, 6", "corneal dystrophy, Fuchs endothelial, type 6", "CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, LATE-ONSET", "corneal dystrophy, Fuchs endothelial, late-onset", "Fuchs' endothelial dystrophy caused by mutation in ZEB1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal dystrophy, Fuchs endothelial, 6", "shortest_name_length": 5}
{"curie": "UMLS:C0277005", "names": ["Opisthorchis Viverrini Infection", "Opisthorchis viverrini Infection", "Opisthorchis viverrini Infections", "Infection, Opisthorchis viverrini", "Infections, Opisthorchis viverrini", "Infection by Opisthorchis viverrini", "Infection caused by Opisthorchis viverrini", "Infection caused by Opisthorchis viverrini (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Opisthorchis viverrini Infection", "shortest_name_length": 32}
{"curie": "MONDO:0001229", "names": ["diverticulitis; bowel, small", "Diverticulitis of Small Bowel", "small intestine diverticulitis", "Diverticulitis of small intestine", "diverticulitis of small intestine", "Diverticulitis of small intestine, NOS", "Diverticulitis of small intestine (disorder)", "diverticulitis of small intestine (diagnosis)", "Diverticulosis of small intestine with hemorrhage", "diverticulosis of small intestine with hemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small intestine diverticulitis", "shortest_name_length": 28}
{"curie": "MONDO:0012180", "names": ["ARVD9", "ARVC9", "arrhythmogenic right ventricular dysplasia 9", "arrhythmogenic right ventricular cardiomyopathy 9", "arrhythmogenic right ventricular dysplasia type 9", "ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 9", "Arrhythmogenic Right Ventricular Cardiomyopathy 9", "familial arrhythmogenic right ventricular dysplasia 9", "Familial Arrhythmogenic Right Ventricular Dysplasia 9", "ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 9", "arrhythmogenic right ventricular dysplasia, familial, 9", "Arrhythmogenic Right Ventricular Dysplasia, Familial, 9", "arrhythmogenic right ventricular dysplasia, familial, type 9", "PKP2 familial isolated arrhythmogenic right ventricular dysplasia", "familial isolated arrhythmogenic right ventricular dysplasia caused by mutation in PKP2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arrhythmogenic right ventricular dysplasia 9", "shortest_name_length": 5}
{"curie": "UMLS:C0347637", "names": ["Adrenal Gland Injury", "Adrenal gland injury", "injury; adrenal gland", "injury of adrenal gland", "gl.suprarenalis; injury", "Injury of adrenal gland", "injury; suprarenal gland", "Injury of suprarenal gland", "Injury of adrenal gland (disorder)", "injury of adrenal gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of adrenal gland", "shortest_name_length": 20}
{"curie": "MONDO:0002338", "names": ["extratemporal epilepsy", "Extratemporal Epilepsy", "Extratemporal epilepsy", "Extratemporal epilepsy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extratemporal epilepsy", "shortest_name_length": 22}
{"curie": "MONDO:0019673", "names": ["PAPA", "Postaxial polydactyly type A", "postaxial polydactyly type A", "Postaxial Polydactyly, Type A", "POSTAXIAL POLYDACTYLY, TYPE A", "Postaxial polydactyly, type A", "postaxial polydactyly type A (disease)", "Postaxial polydactyly type A (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postaxial polydactyly type A", "shortest_name_length": 4}
{"curie": "MONDO:0032864", "names": ["IDDSADF", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, AUTISM, AND DYSMORPHIC FACIES", "intellectual developmental disorder with speech delay, autism, and dysmorphic facies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder with speech delay, autism, and dysmorphic facies", "shortest_name_length": 7}
{"curie": "UMLS:C5557182", "names": ["Stage IVA Cervical Cancer AJCC v9", "Stage IVA Cervical Carcinoma AJCC v9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Cervical Cancer AJCC v9", "shortest_name_length": 33}
{"curie": "MONDO:0006800", "names": ["Classic Apraxia", "Classic apraxia", "classic apraxia", "Apraxia, Classic", "Classic Apraxias", "ideomotor apraxia", "Ideomotor Apraxia", "Ideomotor apraxia", "Apraxias, Classic", "Apraxia, Ideomotor", "Ideomotor Apraxias", "Ideokinetic apraxia", "Ideokinetic Apraxia", "Ideomotor Dyspraxia", "Ideomotor dyspraxia", "Apraxias, Ideomotor", "ideomotor dyspraxia", "Ideokinetic Apraxias", "Apraxia, Ideokinetic", "Limb Kinetic Apraxia", "Ideomotor Dyspraxias", "limb-kinetic apraxia", "Limb-kinetic apraxia", "Dyspraxia, Ideomotor", "transcortical apraxia", "Limb Kinetic Apraxias", "Dyspraxias, Ideomotor", "Apraxia, Limb Kinetic", "Transcortical apraxia", "Kinetic Apraxia, Limb", "Transcortical Apraxia", "Apraxias, Ideokinetic", "Kinetic Apraxias, Limb", "Apraxias, Limb Kinetic", "Transcortical Apraxias", "Apraxia, Transcortical", "Apraxias, Transcortical", "Limb-kinetic apraxia (finding)", "Ideomotor dyspraxia (disorder)", "limb-kinetic apraxia (finding)", "transcortical apraxia (finding)", "Ideomotor dyspraxia (diagnosis)", "Transcortical apraxia (finding)", "classic apraxia (finding) [ambiguous]", "developmental disorder ideomotor dyspraxia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ideomotor apraxia", "shortest_name_length": 15}
{"curie": "UMLS:C5419759", "names": ["Unresectable Hypopharyngeal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Hypopharyngeal Squamous Cell Carcinoma", "shortest_name_length": 51}
{"curie": "UMLS:C1706925", "names": ["Benign Pilar-Associated Mesenchyme Tumor", "Benign Pilar-Associated Mesenchyme Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Pilar-Associated Mesenchyme Neoplasm", "shortest_name_length": 40}
{"curie": "MONDO:0006347", "names": ["pancreatic large cell NEC", "Pancreatic Large Cell NEC", "pancreatic large cell NEC G3", "Pancreatic Large Cell NEC G3", "pancreas large cell neuroendocrine carcinoma", "Pancreatic Large Cell Neuroendocrine Carcinoma", "pancreatic large cell neuroendocrine carcinoma", "large cell neuroendocrine carcinoma of pancreas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic large cell neuroendocrine carcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0001722", "names": ["Central pterygium", "central pterygium", "Central pterygium of eye", "Central pterygium (disorder)", "central pterygium (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central pterygium", "shortest_name_length": 17}
{"curie": "MONDO:0012995", "names": ["MYP15", "Myopia 15", "MYOPIA 15 (disorder)", "myopia 15, autosomal dominant", "MYOPIA 15, AUTOSOMAL DOMINANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopia 15, autosomal dominant", "shortest_name_length": 5}
{"curie": "UMLS:C4331497", "names": ["Ventricular Ependymal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ventricular Ependymal Tumor", "shortest_name_length": 27}
{"curie": "MONDO:0014127", "names": ["OCA5", "Oculocutaneous albinism type 5", "albinism oculocutaneous type 5", "oculocutaneous albinism type 5", "oculocutaneous albinism type V", "albinism, oculocutaneous, type V", "ALBINISM, OCULOCUTANEOUS, TYPE V", "Oculocutaneous albinism type 5 (disorder)", "oculocutaneous albinism type 5 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculocutaneous albinism type 5", "shortest_name_length": 4}
{"curie": "MONDO:0008545", "names": ["Thalassemia, Beta+, Silent Allele", "THALASSEMIA, BETA+, SILENT ALLELE", "thalassemia, beta+, silent allele"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thalassemia, beta+, silent allele", "shortest_name_length": 33}
{"curie": "MONDO:0017697", "names": ["GSDIV, fatal perinatal neuromuscular form", "GSD IV, NEUROMUSCULAR FORM, FATAL PERINATAL", "GSD IV, Neuromuscular Form, Fatal Perinatal", "GSD type 4, fatal perinatal neuromuscular form", "GBE deficiency, fatal perinatal neuromuscular form", "glycogenosis type 4, fatal perinatal neuromuscular form", "Glycogenosis type 4, fatal perinatal neuromuscular form", "Glycogenosis type IV, fatal perinatal neuromuscular form", "glycogenosis type IV, fatal perinatal neuromuscular form", "GLYCOGEN STORAGE DISEASE IV, FATAL PERINATAL NEUROMUSCULAR", "glycogen storage disease type 4, fatal perinatal neuromuscular form", "Glycogen storage disease type 4, fatal perinatal neuromuscular form", "glycogen storage disease type IV, fatal perinatal neuromuscular form", "Glycogen storage disease type IV, fatal perinatal neuromuscular form", "GSD due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form", "glycogenosis due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form", "Glycogenosis due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form", "glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form", "Glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form", "shortest_name_length": 41}
{"curie": "MONDO:0011466", "names": ["WDM", "dystrophy; Gowers", "Gowers; dystrophy", "WELANDER DISTAL MYOPATHY", "Welander Distal Myopathy", "Welander distal myopathy", "MYOPATHY, DISTAL, SWEDISH", "Myopathy, Distal, Swedish", "myopathy, distal, Swedish", "Distal Myopathy, Welander", "GOWERS MUSCULAR DYSTROPHY", "Gowers; muscular dystrophy", "Gower's muscular dystrophy", "muscular; dystrophy, Gowers", "Muscular dystrophy, Gower's", "dystrophy; muscular, Gowers", "Wielander's distal dystrophy", "distal myopathy, Swedish type", "Distal myopathy, Welander type", "distal myopathy, Welander type", "MYOPATHY, LATE DISTAL HEREDITARY", "Myopathia distalis tarda hereditaria", "Welander distal myopathy, Swedish type", "Gower's muscular dystrophy (diagnosis)", "Progressive muscular dystrophy, Gower's type", "Progressive muscular dystrophy, late distal type", "MUSCULAR DYSTROPHY, DISTAL, LATE-ONSET, AUTOSOMAL DOMINANT", "muscular dystrophy, distal, late-onset, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal myopathy, Welander type", "shortest_name_length": 3}
{"curie": "UMLS:C5421222", "names": ["Non-Neoplastic Respiratory System Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Respiratory System Disorder", "shortest_name_length": 42}
{"curie": "MONDO:0018701", "names": ["congenital nemaline myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital nemaline myopathy", "shortest_name_length": 28}
{"curie": "MONDO:0015260", "names": ["Fish tapeworm", "fish tapeworm", "Dibothriocephalus", "Bothriocephalosis", "Diphyllobothriasis", "DIPHYLLOBOTHRIASIS", "Diphyllobothriases", "diphyllobothriasis", "Diphyllobothriosis", "DIBOTHRIOCEPHALIASIS", "FISH TAPEWORM INFECTION", "Fish tapeworm infection", "BROAD TAPEWORM INFECTION", "fish tapeworm; infection", "Fish tapeworm (infection)", "Diphyllobothrium infection", "infestation; fish tapeworm", "Diphyllobothrium Infection", "fish tapeworm; infestation", "Infection, Diphyllobothrium", "Diphyllobothrium Infections", "infestation; tapeworm, fish", "Diphyllobothrium; infestation", "Intestinal diphyllobothriasis", "infestation; Diphyllobothrium", "Diphyllobothriasis (disorder)", "Dibothriocephalus; infestation", "Diphyllobothriasis, intestinal", "infestation; Dibothriocephalus", "Infection by Diphyllobothrium, NOS", "Diphyllobothrium infectious disease", "Diphyllobothrium disease or disorder", "intestinal disorder diphyllobothriasis", "Intestinal diphyllobothriasis (disorder)", "Intestinal diphyllobothriasis (diagnosis)", "Diphyllobothrium caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diphyllobothriasis", "shortest_name_length": 13}
{"curie": "MONDO:0005748", "names": ["Enzootic Calf Pneumonia", "Enzootic Calf Pneumonias", "Calf Pneumonia, Enzootic", "Pneumonia, Enzootic Calf", "Pneumonias, Enzootic Calf", "Enzootic Pneumonia of Calves", "Enzootic pneumonia of calves", "enzootic pneumonia of calves", "Pneumonia of Calves, Enzootic", "Enzootic pneumonia of calves (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "enzootic pneumonia of calves", "shortest_name_length": 23}
{"curie": "MONDO:0010228", "names": ["DFN4", "DFNX3", "X-linked deafness 3", "Deafness, X-Linked 3", "DEAFNESS, X-LINKED 3", "deafness, X-linked 3", "deafness X-linked, DFN3", "hearing loss, X-linked 3", "congenital sensorineural X-linked deafness 4", "DEAFNESS, X-LINKED 4, CONGENITAL SENSORINEURAL", "deafness, X-linked 4, congenital sensorineural", "Deafness, X-Linked 4, Congenital Sensorineural"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, X-linked 3", "shortest_name_length": 4}
{"curie": "UMLS:C4288542", "names": ["Ovarian Retiform Sertoli-Leydig Cell Tumor, Variant with Heterologous Elements"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Retiform Sertoli-Leydig Cell Tumor, Variant with Heterologous Elements", "shortest_name_length": 78}
{"curie": "UMLS:C3273051", "names": ["Bile Duct Intraductal Papillary Neoplasm, High Grade", "Bile Duct Intraductal Papillary Neoplasm, High-Grade", "Bile Duct IPN with High Grade Intraepithelial Neoplasia", "Bile Duct Papillary Neoplasm with High Grade Intraepithelial Neoplasia", "Intraductal Papillary Neoplasm with High Grade Intraepithelial Neoplasia", "Intraductal papillary neoplasm with high grade intraepithelial neoplasia", "Bile Duct Intraductal Papillary Neoplasm with High Grade Intraepithelial Neoplasia", "Intraductal papillary neoplasm with high grade intraepithelial neoplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraductal papillary neoplasm with high grade intraepithelial neoplasia", "shortest_name_length": 52}
{"curie": "UMLS:C0271412", "names": ["blood ear", "ear bleed", "bleed ear", "ear blood", "bleeds ear", "blood ears", "otorrhagia", "Otorrhagia", "Bleeding ear", "blooding ear", "Ear bleeding", "ear bleeding", "bleeding ear", "Bleeding;ear", "EAR BLEEDING", "bleeding ears", "bleedings ear", "ears bleeding", "Ear hemorrhage", "ear hemorrhage", "ear; hemorrhage", "hemorrhage; ear", "Ear haemorrhage", "Bleeding from ear", "Blood in/from ear", "bleeding from ear", "BLEEDING FROM EARS", "Bleeding from ears", "bleeding from ears", "Otorrhagia syndrome", "ear blood discharge", "EAR DISCHARGE BLOOD", "bleeding from the ear", "Bleeding from the ear", "otorrhagia (diagnosis)", "Hemorrhage from the ear", "Haemorrhage from the ear", "Otorrhagia, unspecified ear", "Bleeding from ear (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bleeding from ear", "shortest_name_length": 9}
{"curie": "UMLS:C0155955", "names": ["jaw; exostosis", "exostosis; jaw", "exostosis of jaw", "Exostosis of jaw", "Exostosis of jaw, NOS", "Exostosis of jaw (disorder)", "exostosis of jaw (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Exostosis of jaw", "shortest_name_length": 14}
{"curie": "UMLS:C5419441", "names": ["Drug Resistant Bacterial Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drug Resistant Bacterial Infection", "shortest_name_length": 34}
{"curie": "UMLS:C0026644", "names": ["EDENTULOUS", "edentulous", "Edentulous", "natural teeth", "Toothless Mouth", "Mouth, Toothless", "Edentulous mouth", "No natural teeth", "absence of teeth", "Edentulous Mouth", "Absence of teeth", "Edentulous Mouths", "Mouth, Edentulous", "Edentulous (finding)", "all teeth were absent", "Absence of teeth (finding)", "edentulous (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mouth, Edentulous", "shortest_name_length": 10}
{"curie": "MONDO:0002310", "names": ["Lens in anterior chamber", "anterior dislocation of lens", "Anterior dislocation of lens", "Anterior dislocation of lens (disorder)", "anterior dislocation of lens (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anterior dislocation of lens", "shortest_name_length": 24}
{"curie": "UMLS:C0751184", "names": ["Temporal Region Trauma", "Trauma, Temporal Region", "Temporal Region Traumas", "Traumas, Temporal Region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Temporal Region Trauma", "shortest_name_length": 22}
{"curie": "UMLS:C4763519", "names": ["POLG-Related Spectrum Disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "POLG-Related Spectrum Disorders", "shortest_name_length": 31}
{"curie": "MONDO:0014300", "names": ["MPXPS", "myopathy with extrapyramidal signs", "MYOPATHY WITH EXTRAPYRAMIDAL SIGNS", "proximal myopathy with extrapyramidal signs"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "proximal myopathy with extrapyramidal signs", "shortest_name_length": 5}
{"curie": "MONDO:0002477", "names": ["prostate gland NET", "prostate neuroendocrine neoplasm", "Prostate Neuroendocrine Neoplasm", "prostate neuroendocrine carcinoma", "neuroendocrine neoplasm of prostate", "prostate gland neuroendocrine tumor", "Neuroendocrine Neoplasm of Prostate", "neuroendocrine tumor of the prostate", "prostate gland neuroendocrine neoplasm", "neuroendocrine neoplasm of the prostate", "Neuroendocrine Neoplasm of the Prostate", "neuroendocrine neoplasm of prostate gland", "prostate gland neuroendocrine tumor, well differentiated, low or intermediate grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate neuroendocrine neoplasm", "shortest_name_length": 18}
{"curie": "UMLS:C0869150", "names": ["Late neonatal hypocalcemia", "Late neonatal hypocalcaemia", "Neonatal hypocalcemic tetany", "Neonatal hypocalcaemic tetany", "Hypocalcemic tetany in newborn", "Hypocalcaemic tetany in newborn", "Late neonatal hypocalcemia (disorder)", "Neonatal hypocalcemic tetany (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Late neonatal hypocalcemia", "shortest_name_length": 26}
{"curie": "MONDO:0013449", "names": ["LCA7", "Leber congenital amaurosis 7", "LEBER CONGENITAL AMAUROSIS 7", "CRX Leber congenital amaurosis", "Leber congenital amaurosis type 7", "Leber congenital amaurosis caused by mutation in CRX"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leber congenital amaurosis 7", "shortest_name_length": 4}
{"curie": "MONDO:0011301", "names": ["PHP1B", "PHD1b", "PHP IB", "PHD Ib", "Php 1B", "pseudohypoparathyroidism Ib", "pseudohypoparathyroidism type 1B", "Type Ib Pseudohypoparathyroidism", "pseudohypoparathyroidism type IB", "Pseudohypoparathyroidism type 1B", "Pseudohypoparathyroidism Type 1B", "Pseudohypoparathyroidism Type 1b", "Pseudohypoparathyroidism, Type Ib", "PSEUDOHYPOPARATHYROIDISM, TYPE IB", "pseudohypoparathyroidism, type IB", "pseudohypoparathyroidism, type 1B", "Type Ib Pseudohypoparathyroidisms", "Pseudohypoparathyroidisms, Type Ib", "Renal Parathyroid Hormone Resistance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudohypoparathyroidism type 1B", "shortest_name_length": 5}
{"curie": "MONDO:0017061", "names": ["closed iniencephaly", "Closed iniencephaly", "Iniencephalus clausus", "Iniencephaly - closed", "Iniencephaly - closed (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "closed iniencephaly", "shortest_name_length": 19}
{"curie": "MONDO:0002803", "names": ["hollow visceral myopathy", "intestine pseudoobstruction", "intestinal pseudoobstruction", "Intestinal pseudoobstruction", "Intestinal Pseudo-Obstruction", "intestinal pseudo-obstruction", "Intestinal pseudo-obstruction", "pseudo-obstruction of intestine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intestinal pseudo-obstruction", "shortest_name_length": 24}
{"curie": "UMLS:C0333549", "names": ["Red infarct", "red infarct", "red degeneration", "Red degeneration", "hemorrhagic infarct", "Hemorrhagic infarct", "Haemorrhagic infarct", "Infarct, hemorrhagic", "Hemorrhagic infarction", "hemorrhagic infarction", "Haemorrhagic infarction", "Hemorrhagic infarction (disorder)", "Hemorrhagic infarct (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemorrhagic infarct", "shortest_name_length": 11}
{"curie": "UMLS:C4551540", "names": ["Stage II Vaginal Cancer", "stage II vaginal cancer", "Vaginal Cancer Stage II", "AJCC Stage II Vaginal Cancer", "FIGO Stage II Vagina Carcinoma", "Stage II Vaginal Cancer AJCC v6", "FIGO Stage II Vaginal Carcinoma", "Stage II Vaginal Cancer AJCC v7", "FIGO Stage II Carcinoma of Vagina", "Stage II Vaginal Carcinoma AJCC v6", "Stage II Vaginal Carcinoma AJCC v7", "FIGO Stage II Carcinoma of the Vagina", "Stage II Vaginal Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Vaginal Cancer AJCC v6 and v7", "shortest_name_length": 23}
{"curie": "MONDO:0009041", "names": ["Baraitser Rodeck garner syndrome", "Baraitser Rodeck Garner syndrome", "CRANIOSYNOSTOSIS-MENTAL RETARDATION-CLEFTING SYNDROME", "craniosynostosis-mental retardation-clefting syndrome", "Craniosynostosis Mental Retardation Clefting Syndrome", "craniosynostosis mental retardation clefting syndrome", "craniosynostosis-intellectual disability-clefting syndrome", "craniosynostosis intellectual disability clefting syndrome", "craniosynostosis, mental retardation, seizures, choroidal coloboma, dysplastic kidneys, bat ears, cleft lip and palate, and beaked nose", "craniosynostosis, intellectual disability, seizures, choroidal coloboma, dysplastic kidneys, bat ears, cleft lip and palate, and beaked nose"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniosynostosis-intellectual disability-clefting syndrome", "shortest_name_length": 32}
{"curie": "UMLS:C0751004", "names": ["Giant Intracranial Aneurysm", "Intracranial Aneurysm, Giant", "Giant Intracranial Aneurysms", "Aneurysm, Giant Intracranial", "Intracranial Aneurysms, Giant", "Aneurysms, Giant Intracranial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Giant Intracranial Aneurysm", "shortest_name_length": 27}
{"curie": "MONDO:0003506", "names": ["Pulmonary Artery Syncytioma", "pulmonary artery syncytioma", "syncytioma of pulmonary artery", "Syncytioma of pulmonary artery", "Syncytioma of Pulmonary Artery", "pulmonary artery choriocarcinoma", "Pulmonary Artery Choriocarcinoma", "Syncytioma of the Pulmonary Artery", "Pulmonary Artery Chorioepithelioma", "pulmonary artery chorioepithelioma", "syncytioma of the pulmonary artery", "Choriocarcinoma of Pulmonary Artery", "choriocarcinoma of pulmonary artery", "chorioepithelioma of pulmonary artery", "Chorioepithelioma of Pulmonary Artery", "Choriocarcinoma of the Pulmonary Artery", "choriocarcinoma of the pulmonary artery", "chorioepithelioma of the pulmonary artery", "Chorioepithelioma of the Pulmonary Artery", "pulmonary artery choriocarcinoma (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary artery choriocarcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C0338336", "names": ["Recurrent Visual Pathway Glioma", "recurrent childhood optic tract glioma", "pediatric recurrent optic tract glioma", "childhood recurrent optic tract glioma", "recurrent glioma, pediatric optic tract", "recurrent glioma, childhood optic tract", "recurrent optic tract glioma, pediatric", "recurrent optic nerve glioma, pediatric", "recurrent optic tract glioma, childhood", "Relapsed Pediatric Visual Pathway Glioma", "Relapsed Childhood Visual Pathway Glioma", "optic tract glioma, childhood, recurrent", "glioma, pediatric optic tract, recurrent", "glioma, childhood optic tract, recurrent", "optic tract glioma, pediatric, recurrent", "Recurrent Pediatric Visual Pathway Glioma", "childhood recurrent visual pathway glioma", "Recurrent Childhood Visual Pathway Glioma", "pediatric recurrent visual pathway glioma", "recurrent pediatric visual pathway glioma", "recurrent childhood visual pathway glioma", "recurrent glioma, pediatric visual pathway", "recurrent visual pathway glioma, pediatric", "recurrent glioma, childhood visual pathway", "recurrent visual pathway glioma, childhood", "Relapsed Glioma of Pediatric Visual Pathway", "glioma, childhood visual pathway, recurrent", "visual pathway glioma, pediatric, recurrent", "visual pathway glioma, childhood, recurrent", "Relapsed Glioma of Childhood Visual Pathway", "glioma, pediatric visual pathway, recurrent", "Recurrent Glioma of Childhood Visual Pathway", "Recurrent Glioma of Pediatric Visual Pathway", "Relapsed Glioma of the Pediatric Visual Pathway", "Relapsed Glioma of the Childhood Visual Pathway", "Recurrent Glioma of the Childhood Visual Pathway", "Recurrent Glioma of the Pediatric Visual Pathway", "childhood CNS tumor, recurrent optic tract glioma", "recurrent childhood CNS tumor, optic tract glioma", "recurrent pediatric CNS tumor, optic tract glioma", "pediatric CNS tumor, optic tract glioma, recurrent", "recurrent pediatric brain tumor, optic tract glioma", "recurrent childhood brain tumor, optic tract glioma", "childhood brain tumor, recurrent optic tract glioma", "recurrent pediatric CNS tumor, visual pathway glioma", "pediatric brain tumor, optic tract glioma, recurrent", "recurrent childhood CNS tumor, visual pathway glioma", "childhood CNS tumor, recurrent visual pathway glioma", "pediatric CNS tumor, visual pathway glioma, recurrent", "recurrent childhood brain tumor, visual pathway glioma", "recurrent pediatric brain tumor, visual pathway glioma", "childhood brain tumor, recurrent visual pathway glioma", "pediatric brain tumor, visual pathway glioma, recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Visual Pathway Glioma", "shortest_name_length": 31}
{"curie": "UMLS:C5237211", "names": ["Locally Advanced Squamous Cell Carcinoma of Unknown Primary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Squamous Cell Carcinoma of Unknown Primary", "shortest_name_length": 59}
{"curie": "MONDO:0012594", "names": ["CFID", "C3G2", "C3 GLOMERULOPATHY 2", "factor I deficiency", "Factor I deficiency", "C3G2 C3 glomerulopathy 2", "C3 Inactivator Deficiency", "C3 inactivator deficiency", "C3 INACTIVATOR DEFICIENCY", "Complement Factor I Deficiency", "complement factor I deficiency", "complement Factor 1 deficiency", "COMPLEMENT FACTOR I DEFICIENCY", "Factor I deficiency (disorder)", "Complement factor 3i deficiency", "factor I deficiency (diagnosis)", "immunodeficiency with factor I anomaly", "COMPLEMENT COMPONENT 3 INACTIVATOR DEFICIENCY", "complement component 3 inactivator deficiency", "Complement component 3 inactivator deficiency", "Complement Component 3 Inactivator Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complement factor I deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0011700", "names": ["IBD6", "inflammatory bowel disease 6", "Inflammatory Bowel Disease 6", "INFLAMMATORY BOWEL DISEASE 6", "inflammatory bowel disease type 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory bowel disease 6", "shortest_name_length": 4}
{"curie": "MONDO:0030607", "names": ["BRYLIB2", "Bryant-Li-Bhoj neurodevelopmental syndrome 2", "BRYANT-LI-BHOJ NEURODEVELOPMENTAL SYNDROME 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bryant-Li-Bhoj neurodevelopmental syndrome 2", "shortest_name_length": 7}
{"curie": "UMLS:C1306632", "names": ["gastrointestinal tract malignant neoplasm primary", "Primary malignant neoplasm of gastrointestinal tract", "Primary malignant neoplasm of gastrointestinal tract (disorder)", "Primary malignant neoplasm of gastrointestinal tract (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary malignant neoplasm of gastrointestinal tract", "shortest_name_length": 49}
{"curie": "UMLS:C5236081", "names": ["Refractory Clear Cell Renal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Clear Cell Renal Cell Carcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0004831", "names": ["Proliferative fasciitis", "Proliferative Fasciitis", "proliferative fasciitis", "Proliferative fasciitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "proliferative fasciitis", "shortest_name_length": 23}
{"curie": "UMLS:C4317339", "names": ["JAE", "juvenile absence seizure", "Epilepsy Juvenile Absence", "Juvenile Absence Epilepsy", "Juvenile absence epilepsy", "Absence Epilepsy, Juvenile", "Epilepsy, Juvenile Absence", "juvenile absence seizure (diagnosis)", "Juvenile absence epilepsy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Juvenile Absence Epilepsy", "shortest_name_length": 3}
{"curie": "UMLS:C4552017", "names": ["Stage IIIB", "Stage IIIB Cancer of Testis", "stage IIIB cancer of testis", "Stage IIIB Testicular Cancer", "stage IIIB testicular cancer", "Stage IIIB Cancer of the Testis", "stage IIIB cancer of the testis", "stage IIIB testicular cancer AJCC v7", "Stage IIIB Testicular Cancer AJCC v7", "Stage IIIB Testicular Cancer AJCC v6", "stage IIIB testicular cancer AJCC v6", "Stage IIIB Testicular Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Testicular Cancer AJCC v6 and v7", "shortest_name_length": 10}
{"curie": "MONDO:0044906", "names": ["bladder urothelial papilloma", "Bladder Urothelial Papilloma", "bladder transitional cell papilloma", "Bladder Transitional Cell Papilloma", "urinary bladder urothelial papilloma", "bladder; papilloma transitional cell", "Urinary Bladder Urothelial Papilloma", "transitional cell; papilloma, bladder", "papilloma; transitional cell, bladder", "urinary bladder transitional cell papilloma", "Urinary Bladder Transitional Cell Papilloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder urothelial papilloma", "shortest_name_length": 28}
{"curie": "MONDO:0006216", "names": ["Gallbladder Adenoma", "gallbladder adenoma", "Gallbladder adenoma", "GALLBLADDER, ADENOMA", "gall bladder adenoma", "Adenoma of Gallbladder", "Adenoma of gallbladder", "adenoma of gallbladder", "Adenoma of the Gallbladder", "adenoma of the gallbladder", "Adenoma of gallbladder (disorder)", "adenoma of gallbladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gallbladder adenoma", "shortest_name_length": 19}
{"curie": "MONDO:0400002", "names": ["milk-alkali syndrome", "calcium-alkali syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "calcium-alkali syndrome", "shortest_name_length": 20}
{"curie": "MONDO:0035403", "names": ["serous cystadenoma of childhood", "Serous cystadenoma of ovary in childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "serous cystadenoma of childhood", "shortest_name_length": 31}
{"curie": "MONDO:0006727", "names": ["diastolic failure heart", "diastolic heart failure", "heart failure diastolic", "Diastolic Heart Failure", "Diastolic heart failure", "Heart Failure, Diastolic", "Diastolic Heart Failures", "Diastolic heart failure (disorder)", "Diastolic heart failure, unspecified", "Heart Failure, Normal Ejection Fraction", "Heart Failure, Preserved Ejection Fraction", "Unspecified diastolic (congestive) heart failure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diastolic heart failure", "shortest_name_length": 23}
{"curie": "MONDO:0014841", "names": ["TTD6", "nonphotosensitive trichothiodystrophy 6", "TRICHOTHIODYSTROPHY 6, NONPHOTOSENSITIVE", "trichothiodystrophy 6, nonphotosensitive", "GTF2E2 nonphotosensitive trichothiodystrophy", "trichothiodystrophy 6, nonphotosensitive; TTD6", "nonphotosensitive trichothiodystrophy caused by mutation in GTF2E2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichothiodystrophy 6, nonphotosensitive", "shortest_name_length": 4}
{"curie": "UMLS:C3274794", "names": ["Primary Valvular Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Valvular Disorder", "shortest_name_length": 25}
{"curie": "UMLS:C4761612", "names": ["CHIP", "Clonal Hematopoiesis of Indeterminate Potential", "CHIP Clonal Hematopoiesis of Indeterminate Potential"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clonal Hematopoiesis of Indeterminate Potential", "shortest_name_length": 4}
{"curie": "MONDO:0019824", "names": ["non-acquired pituitary hormone deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-acquired pituitary hormone deficiency", "shortest_name_length": 41}
{"curie": "MONDO:0018639", "names": ["caudal regression-sirenomelia spectrum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "caudal regression-sirenomelia spectrum", "shortest_name_length": 38}
{"curie": "MONDO:0011848", "names": ["BSH", "HSA", "orgasmic cephalgia", "benign sexual headache", "BENIGN SEXUAL HEADACHE", "headache precipitated by sex", "orgasmic cephalgia (diagnosis)", "headache precipitated by sex (symptom)", "Headache associated with sexual activity", "HEADACHE ASSOCIATED WITH SEXUAL ACTIVITY", "headache associated with sexual activity", "Headache associated with sexual activity (finding)", "headache associated with sexual activity (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "headache associated with sexual activity", "shortest_name_length": 3}
{"curie": "UMLS:C2981404", "names": ["Stage IVA Colorectal Cancer", "Stage IVA Colorectal Cancer AJCC v7", "Stage IVA Colorectal (Colon or Rectal) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Colorectal Cancer AJCC v7", "shortest_name_length": 27}
{"curie": "UMLS:C0235656", "names": ["lesion cervix", "cervix lesion", "CERVIX LESION", "Cervix lesion", "cervix lesions", "cervical lesion", "Cervical Lesion", "CERVICAL LESION", "lesion cervical", "lesion of cervix", "cervical lesions", "Lesion of cervix", "cervical; lesion", "lesion; cervical", "Uterine cervical lesion", "Lesion of the Cervix Uteri", "Lesion of cervix (disorder)", "cervical lesion (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lesion of cervix", "shortest_name_length": 13}
{"curie": "UMLS:C2827349", "names": ["Renal Benign Mesenchymoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal Benign Mesenchymoma", "shortest_name_length": 25}
{"curie": "MONDO:0007260", "names": ["CAR FACTOR DEFICIENCY", "Car factor deficiency", "Car Factor Deficiency", "Car. Factor Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Car factor deficiency", "shortest_name_length": 21}
{"curie": "MONDO:0002528", "names": ["Synovial Tumor", "synovial tumor", "Synovial neoplasm", "tumor of Synovium", "Synovial Neoplasm", "synovial neoplasm", "synovium neoplasm", "Tumor of Synovium", "tumor of synovium", "Synovial Neoplasms", "neoplasm of synovia", "neoplasm of synovium", "Neoplasm of Synovium", "tumor of the synovium", "Tumor of the Synovium", "neoplasm of the synovium", "Neoplasm of the Synovium", "neoplasm of synovia (diagnosis)", "synovial membrane of synovial joint tumor", "synovial neoplasm (morphologic abnormality)", "tumor of synovial membrane of synovial joint", "synovial membrane of synovial joint neoplasm", "synovial neoplasm NOS (morphologic abnormality)", "neoplasm of synovial membrane of synovial joint", "synovial membrane of synovial joint neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "synovium neoplasm", "shortest_name_length": 14}
{"curie": "MONDO:0700077", "names": ["VAMAS6", "vitiligo-associated multiple autoimmune disease susceptibility 6", "VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitiligo-associated multiple autoimmune disease susceptibility 6", "shortest_name_length": 6}
{"curie": "MONDO:0000292", "names": ["philophthalmiasis", "Philophthalmus infectious disease", "Philophthalmus disease or disorder", "Philophthalmus caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "philophthalmiasis", "shortest_name_length": 17}
{"curie": "UMLS:C0005604", "names": ["Birth trauma", "injury birth", "birth trauma", "trauma birth", "Birth injury", "Birth Injury", "birth injury", "Birth Trauma", "BIRTH TRAUMA", "TRAUMA BIRTH", "injury; birth", "Injury, birth", "birth; injury", "Injury, Birth", "birth injuries", "Birth Injuries", "Birth injuries", "birthing trauma", "traumatic birth", "Injuries, Birth", "Birth injury NOS", "Injuries (Birth)", "Birth injury, NOS", "birthing injuries", "Birth trauma, NOS", "Birth trauma of fetus", "Neonatal Birth Injury", "Birth trauma of foetus", "Birth trauma (P10-P15)", "birth trauma (diagnosis)", "Unspecified birth trauma", "Birth injury, unspecified", "Birth trauma, unspecified", "Birth trauma of fetus (disorder)", "Neonatal Injury Related to Birth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Birth Injuries", "shortest_name_length": 12}
{"curie": "MONDO:0012056", "names": ["LCA9", "LEBER CONGENITAL AMAUROSIS 9", "Leber Congenital Amaurosis 9", "Leber congenital amaurosis 9", "Leber congenital amaurosis type 9", "NMNAT1 Leber congenital amaurosis", "Leber congenital amaurosis, type 9", "amaurosis congenita of Leber, type 9", "Amaurosis congenita of Leber, type 9", "LEBER CONGENITAL AMAUROSIS 9 (disorder)", "Leber congenital amaurosis caused by mutation in NMNAT1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leber congenital amaurosis 9", "shortest_name_length": 4}
{"curie": "MONDO:0018608", "names": ["PAF", "autonomic failure", "Autonomic failure", "Pure dysautonomia", "pure autonomic failure", "Pure Autonomic Failure", "Pure autonomic failure", "Autonomic Failure, Pure", "AUTONOMIC FAILURE, PURE", "Bradbury Eggleston Syndrome", "Bradbury Eggleston syndrome", "Bradbury-Eggleston Syndrome", "Pure idiopatic dysautonomia", "Bradbury-Eggleston syndrome", "bradbury-eggleston syndrome", "Syndrome, Bradbury-Eggleston", "Pure autonomic failure (disorder)", "idiopathic orthostatic hypotension", "Idiopathic orthostatic hypotension", "orthostatic hypotension (a symptom)", "idiopathic orthostatic hypotension (diagnosis)", "idiopathic orthostatic hypotension (a symptom)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pure autonomic failure", "shortest_name_length": 3}
{"curie": "MONDO:0020044", "names": ["autosomal recessive metabolic cerebellar ataxia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive metabolic cerebellar ataxia", "shortest_name_length": 47}
{"curie": "MONDO:0014371", "names": ["DEE23", "EIEE23", "early infantile epileptic encephalopathy 23", "epileptic encephalopathy, early infantile, 23", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 23", "developmental and epileptic encephalopathy 23", "developmental and epileptic encephalopathy, 23", "epileptic encephalopathy, early infantile, type 23", "Epilepsy-cortical blindness-intellectual disability-facial dysmorphism syndrome", "epilepsy-cortical blindness-intellectual disability-facial dysmorphism syndrome", "Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome", "early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 23", "shortest_name_length": 5}
{"curie": "MONDO:0020342", "names": ["NEM3", "actin myopathy", "Actin Myopathy", "Actin myopathy", "Nemaline Myopathy 3", "Nemaline myopathy 3", "NEMALINE MYOPATHY 3", "Actin-Accumulation Myopathy", "Actin accumulation myopathy", "Actin Filament Aggregate Myopathy", "Actin accumulation myopathy (disorder)", "Congenital myopathy with excess thin filaments", "Congenital Myopathy with Excess of Thin Filaments", "Congenital myopathy with excess of thin filaments", "congenital myopathy with excess of thin filaments", "Nemaline myopathy caused by mutation in the alpha-actin gene"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myopathy with excess of thin filaments", "shortest_name_length": 4}
{"curie": "MONDO:0043277", "names": ["trisomy 6", "Trisomy 6", "mosaic trisomy 6", "trisomy 6 mosaicism", "Trisomy 6 (disorder)", "trisomy 6 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mosaic trisomy 6", "shortest_name_length": 9}
{"curie": "MONDO:0024352", "names": ["respiratory virus infection", "viral respiratory infection", "Viral respiratory infection", "respiratory viral infection", "respiratory infection virus", "infections respiratory viral", "Viral Respiratory Tract Infection", "RESPIRATORY TRACT INFECTION VIRAL", "Respiratory tract infection viral", "viral respiratory tract infection", "Respiratory tract infection viral NOS", "Viral respiratory infection (disorder)", "viral respiratory tract infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "viral respiratory tract infection", "shortest_name_length": 27}
{"curie": "MONDO:0021503", "names": ["Benign Gallbladder Tumor", "benign gallbladder tumor", "Gallbladder Benign Tumor", "gallbladder benign tumor", "gallbladder benign neoplasm", "benign tumor of gallbladder", "Benign tumor of gallbladder", "Benign Tumor of Gallbladder", "Gallbladder Benign Neoplasm", "Benign Gallbladder Neoplasm", "benign gallbladder neoplasm", "Benign tumour of gallbladder", "gall bladder benign neoplasm", "benign neoplasm of gallbladder", "Benign neoplasm of gallbladder", "Benign Neoplasm of Gallbladder", "Benign Tumor of the Gallbladder", "benign tumor of the gallbladder", "Benign Neoplasm of the Gallbladder", "benign neoplasm of the gallbladder", "Benign neoplasm of gallbladder (disorder)", "benign neoplasm of gallbladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of gallbladder", "shortest_name_length": 24}
{"curie": "MONDO:0017817", "names": ["localized AL amyloidosis", "primary localized amyloidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary localized amyloidosis", "shortest_name_length": 24}
{"curie": "MONDO:0013615", "names": ["CRSDA", "Kreiborg Pakistani syndrome", "KREIBORG-PAKISTANI SYNDROME", "Kreiborg-Pakistani syndrome", "craniosynostosis-dental anomalies", "Craniosynostosis-dental anomalies", "craniosynostosis and dental anomalies", "CRANIOSYNOSTOSIS AND DENTAL ANOMALIES", "Craniosynostosis and dental anomalies syndrome", "Craniosynostosis and dental anomalies syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniosynostosis and dental anomalies", "shortest_name_length": 5}
{"curie": "MONDO:0023204", "names": ["FCMD", "Fukuda-Miyanomae-Nakata syndrome", "Fukuyama type muscular dystrophy", "Cerebromuscular dystrophy, Fukuyama type", "muscular dystrophy, congenital, Fukuyama type", "muscular dystrophy, congenital progressive, with mental retardation", "muscular dystrophy, congenital, with central nervous system involvement", "muscular dystrophy, congenital progressive, with intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fukuda-Miyanomae-Nakata syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0001697", "names": ["DYSLEXIA", "dyslexia", "Dyslexic", "dyslexic", "Dyslexia", "Dyslexias", "Dyslexia, NOS", "Word Blindness", "word blindness", "Word blindness", "Blindness, Word", "Reading Disorder", "disorder reading", "reading disorder", "Word Blindnesses", "Reading disorder", "Reading Disorders", "Disorder, Reading", "disorder; reading", "reading; disorder", "Blindnesses, Word", "impairment reading", "Dyslexia (finding)", "READING IMPAIRMENT", "Disorders, Reading", "Reading disability", "reading impairment", "impairment readings", "developmental dyslexia", "Developmental dyslexia", "Developmental Dyslexia", "developmental; dyslexia", "dyslexia; developmental", "Dyslexia, Developmental", "Developmental Dyslexias", "Dyslexias, Developmental", "reading learning disability", "Specific reading difficulty", "Specific reading retardation", "development; reading disorder", "developmental reading disorder", "Dyslexia, learning disturbance", "Developmental Reading Disorder", "Developmental reading disorder", "Developmental Reading Disorders", "Reading Disorder, Developmental", "developmental disorder; reading", "reading; developmental disorder", "Disorder, Developmental Reading", "reading disorder; developmental", "Disorders, Developmental Reading", "Developmental Reading Disability", "Reading Disorders, Developmental", "Disability, Developmental Reading", "Developmental dyslexia (disorder)", "Reading Disability, Developmental", "Basic learning disability, reading", "Developmental Reading Disabilities", "developmental dyslexia (diagnosis)", "Disabilities, Developmental Reading", "Reading Disabilities, Developmental", "reading comprehension limited (dyslexia)", "learning; developmental disorder, reading", "Developmental reading disorder (disorder)", "developmental reading disorder (diagnosis)", "Developmental reading disorder, unspecified", "Other specific developmental reading disorder", "reading learning disability (physical finding)", "developmental disorder; learning, learning, reading", "disturbance; reading, developmental disorder (specific)", "reading comprehension limited (dyslexia) (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "reading disorder", "shortest_name_length": 8}
{"curie": "UMLS:C5418791", "names": ["Locally Advanced Oropharyngeal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Oropharyngeal Carcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0003130", "names": ["Mesoblastic nephroma", "mesoblastic nephroma", "Mesoblastic Nephroma", "Nephroma, Mesoblastic", "mesoblastic; nephroma", "nephroma; mesoblastic", "Nephromas, Mesoblastic", "[M]Mesoblastic nephroma", "Mesoblastic nephroma (disorder)", "mesoblastic nephroma (diagnosis)", "Mesoblastic nephroma (morphologic abnormality)", "mesoblastic nephroma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mesoblastic nephroma", "shortest_name_length": 20}
{"curie": "MONDO:0030604", "names": ["malignant cystic nephroma", "Malignant cystic nephroma", "Malignant Cystic Nephroma", "malignant cystic nephroma of kidney", "Malignant cystic nephroma (disorder)", "Malignant Multilocular Cystic Nephroma", "malignant multilocular cystic nephroma", "Malignant multilocular cystic nephroma", "cystic partially differentiated nephroblastoma", "Cystic Partially Differentiated Nephroblastoma", "Cystic partially differentiated nephroblastoma", "malignant cystic nephroma of kidney (diagnosis)", "Malignant cystic nephroma (morphologic abnormality)", "Cystic Partially Differentiated Kidney Nephroblastoma", "Cystic partially differentiated nephroblastoma of kidney", "Cystic partially differentiated nephroblastoma of kidney (disorder)", "Cystic partially differentiated nephroblastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cystic partially differentiated nephroblastoma", "shortest_name_length": 25}
{"curie": "UMLS:C0553686", "names": ["Hernia cerebri", "herniation brain", "Brain herniation", "brain herniation", "brain; herniation", "herniation; brain", "Herniation, brain", "CRANIAL HERNIATION", "cerebral herniation", "Cerebral herniation", "cerebral; herniation", "herniation; cerebral", "Cerebral herniation (disorder)", "cerebral herniation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebral herniation", "shortest_name_length": 14}
{"curie": "UMLS:C0475591", "names": ["Intraventricular Hemorrhage of Newborn Grade 3", "grade III intraventricular hemorrhage neonatal", "grade III neonatal intraventricular hemorrhage", "Grade 3 Intraventricular Hemorrhage of the Newborn", "grade III neonatal intraventricular hemorrhage (diagnosis)", "Intraventricular Hemorrhage of the Newborn with Ventricular Dilatation", "Grade 3 Intraventricular (Nontraumatic) Hemorrhage of Fetus and Newborn", "Intraventricular (nontraumatic) hemorrhage, grade 3, of fetus and newborn", "Intraventricular (Nontraumatic) Hemorrhage, Grade 3, of Fetus and Newborn", "Intraventricular (nontraumatic) haemorrhage, grade 3, of fetus and newborn", "Intraventricular (nontraumatic) haemorrhage, grade 3, of foetus and newborn", "Intraventricular (nontraumatic) hemorrhage, grade 3, of fetus and newborn (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraventricular (nontraumatic) hemorrhage, grade 3, of fetus and newborn", "shortest_name_length": 46}
{"curie": "MONDO:0011572", "names": ["T1D18", "IDDM18", "TYPE 1 DIABETES MELLITUS 18", "type 1 diabetes mellitus 18", "insulin-dependent diabetes mellitus 18", "Insulin-Dependent Diabetes Mellitus 18", "INSULIN-DEPENDENT DIABETES MELLITUS 18", "DIABETES MELLITUS, INSULIN-DEPENDENT, 18", "diabetes mellitus, insulin-dependent, 18", "Diabetes Mellitus, Insulin-Dependent, 18"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type 1 diabetes mellitus 18", "shortest_name_length": 5}
{"curie": "UMLS:C0015379", "names": ["Extravasation of Diagnostic, Therapeutic Materials", "Extravasation of Diagnostic and Therapeutic Materials"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extravasation of Diagnostic and Therapeutic Materials", "shortest_name_length": 50}
{"curie": "MONDO:0006694", "names": ["Atherosclerosis cerebral", "cerebral atherosclerosis", "Cerebral Atherosclerosis", "CEREBRAL ATHEROSCLEROSIS", "Cerebral atherosclerosis", "Cerebral Atheroscleroses", "Atherosclerosis, Cerebral", "Atheroscleroses, Cerebral", "Cerebral vascular atherosclerosis", "Cerebral atherosclerosis (disorder)", "ICAS - intracranial atherosclerosis", "cerebral atherosclerosis (diagnosis)", "Atherosclerosis of intracranial artery", "ATHEROSCLEROTIC CEREBROVASCULAR DISEASE", "ICAD - intracranial atherosclerotic disease", "disease (or disorder); cerebrovascular, arteriosclerotic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral atherosclerosis", "shortest_name_length": 24}
{"curie": "MONDO:0013771", "names": ["HTGTI", "HYPERTRIGLYCERIDEMIA, TRANSIENT INFANTILE", "hypertriglyceridemia, transient infantile", "transient infantile hypertriglyceridemia and fatty liver", "transient infantile hypertriglyceridemia and hepatosteatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transient infantile hypertriglyceridemia and hepatosteatosis", "shortest_name_length": 5}
{"curie": "MONDO:0006682", "names": ["Brachial neuritis", "BRACHIAL NEURITIS", "brachial neuritis", "neuritis brachial", "Brachial Neuritis", "Neuritis, Brachial", "Brachial Neuritides", "Neuritides, Brachial", "neuralgic amyotrophy", "neuritis brachial nos", "BRACHIAL NEURITIS NOS", "amyotrophic neuralgia", "Brachial neuritis, NOS", "Parsonage-Aldren-Turner", "acute shoulder neuritis", "acute brachial neuritis", "shoulder-girdle syndrome", "Shoulder-girdle syndrome", "brachial plexus neuritis", "shoulder girdle syndrome", "Shoulder girdle syndrome", "Brachial plexus neuritis", "Brachial Plexus Neuritis", "brachial neuritis plexus", "Neuritis, Brachial Plexus", "Parsonage Turner Syndrome", "parsonage-turner syndrome", "Parsonage-Turner syndrome", "parsonage turner syndrome", "parsonage Turner syndrome", "Parsonage-Turner Syndrome", "Shoulder Girdle Neuropathy", "parsonage syndrome turners", "Syndrome, Parsonage-Turner", "Brachial Plexus Neuritides", "Shoulder-Girdle Neuropathy", "Neuropathy, Shoulder-Girdle", "Neuropathy, Shoulder Girdle", "Neuritides, Brachial Plexus", "Girdle Neuropathy, Shoulder", "Brachial neuritis (disorder)", "Shoulder Girdle Neuropathies", "Shoulder-Girdle Neuropathies", "brachial neuritis (diagnosis)", "Neuropathies, Shoulder Girdle", "Neuropathies, Shoulder-Girdle", "Girdle Neuropathies, Shoulder", "brachial nerve plexus neuritis", "idiopathic neuralgic amyotrophy", "parsonage-Aldren-Turner syndrome", "acute brachial neuritis syndrome", "parsonage-aldren-turner syndrome", "Parsonage Aldren Turner Syndrome", "Parsonage-Aldren-Turner syndrome", "Parsonage-Aldren-Turner Syndrome", "neuritis of brachial nerve plexus", "Syndrome, Parsonage-Aldren-Turner", "acute brachial radiculitis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachial plexus neuritis", "shortest_name_length": 17}
{"curie": "UMLS:C3714619", "names": ["Insulin Resistance Syndrome", "insulin resistance syndrome", "Insulin resistance syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Insulin resistance syndrome", "shortest_name_length": 27}
{"curie": "MONDO:0003124", "names": ["testis Leydig cell tumor", "Leydig cell tumor of testis", "Leydig Cell Tumor of Testis", "Testicular Leydig Cell Tumor", "testicular Leydig cell tumor", "Leydig cell neoplasm of testis", "Leydig Cell Neoplasm of Testis", "testicular Leydig cell neoplasm", "Leydig Cell Tumor of the Testis", "Leydig cell tumor of the testis", "Testicular Leydig Cell Neoplasm", "Leydig cell tumour of the testis", "Leydig Cell Neoplasm of the Testis", "Leydig cell neoplasm of the testis", "Leydig cell tumor of testis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular Leydig cell tumor", "shortest_name_length": 24}
{"curie": "MONDO:0043294", "names": ["Linear morphea", "linear morphea", "Linear morphoea", "en coup de sabre", "Linear scleroderma", "linear scleroderma", "linear Scleroderma", "scleroderma linear", "Linear Scleroderma", "linear; scleroderma", "scleroderma; linear", "Scleroderma, linear", "Scleroderma, Linear", "Linear scleroderma (disorder)", "linear scleroderma (diagnosis)", "Frontal Linear Scleroderma en Coup de Sabre"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "linear scleroderma", "shortest_name_length": 14}
{"curie": "UMLS:C0751414", "names": ["Secondary Vascular Parkinson Disease", "Parkinson Disease, Secondary Vascular"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parkinson Disease, Secondary Vascular", "shortest_name_length": 36}
{"curie": "MONDO:0009148", "names": ["Zlotogora-Ogur syndrome", "Rosselli-Gulienetti Syndrome", "ROSSELLI-GULIENETTI SYNDROME", "Rosselli-Gulienetti syndrome", "ectodermal dysplasia-cleft lip and palate-mental retardation-syndactyly syndrome I", "ectodermal dysplasia-cleft lip and palate-hand and foot deformity-mental retardation syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rosselli-Gulienetti syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0010966", "names": ["ACG1B", "achondrogenesis Ib", "Achondrogenesis type 1B", "achondrogenesis type IB", "achondrogenesis type 1B", "Achondrogenesis, Type Ib", "Fraccaro achondrogenesis", "Achondrogenesis, type IB", "ACHONDROGENESIS, TYPE IB", "achondrogenesis, type 1B", "achondrogenesis, type IB", "achondrogenesis Fraccaro type", "achondrogenesis, Fraccaro type", "ACHONDROGENESIS, FRACCARO TYPE", "Achondrogenesis, Fraccaro type", "Achondrogenesis, type IB (disorder)", "Achondrogenesis, Parenti-Fraccaro type", "achondrogenesis, Parenti-Fraccaro type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "achondrogenesis type IB", "shortest_name_length": 5}
{"curie": "MONDO:0013438", "names": ["PCCA", "PCH2D", "pontocerebellar hypoplasia type 2D", "PONTOCEREBELLAR HYPOPLASIA, TYPE 2D", "pontocerebellar hypoplasia, type 2D", "Progressive cerebello-cerebral atrophy", "Cerebellocerebral atrophy, progressive", "CEREBELLOCEREBRAL ATROPHY, PROGRESSIVE", "cerebello-cerebral atrophy, progressive", "PCCA - progressive cerebello-cerebral atrophy", "SEPSECS non-syndromic pontocerebellar hypoplasia", "Progressive cerebello-cerebral atrophy (disorder)", "non-syndromic pontocerebellar hypoplasia caused by mutation in SEPSECS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pontocerebellar hypoplasia type 2D", "shortest_name_length": 4}
{"curie": "MONDO:0001623", "names": ["cicatricial lagophthalmos", "Cicatricial Lagophthalmos", "Cicatricial lagophthalmos", "Lagophthalmos, Cicatricial", "Eyelids stay open due to scarring", "Cicatricial lagophthalmos (finding)", "cicatricial lagophthalmos (disease)", "cicatricial lagophthalmos (diagnosis)", "cicatricial lagophthalmos was observed", "cicatricial lagophthalmos (physical finding)", "Inability to close the eyelids due to scarring"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cicatricial lagophthalmos", "shortest_name_length": 25}
{"curie": "MONDO:0024547", "names": ["PAGEN", "Pagen", "PAGEN1", "PANCREATIC AGENESIS 1", "pancreatic agenesis 1", "PDX1 pancreatic agenesis", "PANCREATIC HYPOPLASIA, CONGENITAL", "pancreatic hypoplasia, congenital", "pancreatic agenesis caused by mutation in PDX1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic agenesis 1", "shortest_name_length": 5}
{"curie": "UMLS:C5418772", "names": ["Recurrent Fallopian Tube Undifferentiated Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Fallopian Tube Undifferentiated Carcinoma", "shortest_name_length": 51}
{"curie": "MONDO:0015368", "names": ["neuro-ophthalmological disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuro-ophthalmological disease", "shortest_name_length": 30}
{"curie": "MONDO:0044744", "names": ["PKKD", "PKK DEFICIENCY", "Fletcher trait", "PKK Deficiency", "fletcher trait", "Prekallikrein Deficiency", "prekallikrein deficiency", "Prekallikrein deficiency", "PREKALLIKREIN DEFICIENCY", "Fletcher Factor Deficiency", "fletcher factor deficiency", "Fletcher factor deficiency", "FLETCHER FACTOR DEFICIENCY", "Prekallikrein deficiency (disorder)", "Congenital prekallikrein deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prekallikrein deficiency", "shortest_name_length": 4}
{"curie": "UMLS:C5669740", "names": ["Lipidized Glioblastoma", "Heavily Lipidized Glioblastoma", "Malignant Glioma with Heavily Lipidized (Foamy) Tumor Cells"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lipidized Glioblastoma", "shortest_name_length": 22}
{"curie": "UMLS:C0280161", "names": ["Stage III Diffuse Mixed Cell Lymphoma", "Stage III Adult Diffuse Mixed Cell Lymphoma", "stage III adult diffuse mixed cell lymphoma", "Adult Diffuse Mixed Cell Lymphoma Stage III", "adult diffuse mixed cell lymphoma, stage III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Adult Diffuse Mixed Cell Lymphoma", "shortest_name_length": 37}
{"curie": "MONDO:0015516", "names": ["De Smet-Fabry-Fryns syndrome", "symbrachydactyly of hands and feet"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "symbrachydactyly of hands and feet", "shortest_name_length": 28}
{"curie": "MONDO:0007561", "names": ["EDM1", "MED1", "epiphyseal dysplasia multiple 1", "Polyepiphyseal dysplasia type 1", "multiple epiphyseal dysplasia 1", "polyepiphyseal dysplasia type 1", "epiphyseal dysplasia, multiple, 1", "EPIPHYSEAL DYSPLASIA, MULTIPLE, 1", "Epiphyseal dysplasia, multiple, 1", "Epiphyseal Dysplasia, Ribbing Type", "epiphyseal dysplasia, ribbing type", "EPIPHYSEAL DYSPLASIA, RIBBING TYPE", "epiphyseal dysplasia, Fairbank type", "Multiple epiphyseal dysplasia type 1", "multiple epiphyseal dysplasia type 1", "epiphyseal dysplasia, multiple, type 1", "multiple epiphyseal dysplasia COMP-related", "multiple epiphyseal dysplasia, Comp-related", "Multiple epiphyseal dysplasia, COMP-related", "MULTIPLE EPIPHYSEAL DYSPLASIA, COMP-RELATED", "COMP multiple epiphyseal dysplasia (disease)", "Multiple epiphyseal dysplasia type 1 (disorder)", "multiple epiphyseal dysplasia (disease) caused by mutation in COMP", "Multiple epiphyseal dysplasia, cartilage oligomeric matrix protein related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple epiphyseal dysplasia type 1", "shortest_name_length": 4}
{"curie": "MONDO:0016664", "names": ["Drug Induced Vasculitis", "drug induced vasculitis", "drug-induced vasculitis", "Drug Induced Cutaneous Vasculitis", "drug induced cutaneous vasculitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "drug-induced vasculitis", "shortest_name_length": 23}
{"curie": "MONDO:0012682", "names": ["IMD35", "TYK2 DEFICIENCY", "TYK2 Deficiency", "TYK2 deficiency", "immunodeficiency 35", "IMMUNODEFICIENCY 35", "immunodeficiency type 35", "Tyrosine Kinase 2 Deficiency", "TYROSINE KINASE 2 DEFICIENCY", "tyrosine kinase 2 deficiency", "Susceptibility to infection due to TYK2 deficiency", "susceptibility to infection due to TYK2 deficiency", "autosomal recessiv HIES with atypical mycobacteriosis", "HIES WITH ATYPICAL MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE", "HIES with Atypical Mycobacteriosis, Autosomal Recessive", "HIES with atypical Mycobacteriosis, autosomal recessive", "autosomal recessive hyper-IgE syndrome due to TYK2 deficiency", "Autosomal recessive hyper-IgE syndrome due to TYK2 deficiency", "Susceptibility to infection due to tyrosine kinase 2 deficiency", "autosomal recessive hyper-IgE syndrome with atypical mycobacteriosis", "HYPER-IgE SYNDROME WITH ATYPICAL MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE", "Hyper-IgE Syndrome with Atypical Mycobacteriosis, Autosomal Recessive", "hyper-IgE syndrome with atypical Mycobacteriosis, autosomal recessive", "Susceptibility to infection due to tyrosine kinase 2 deficiency (disorder)", "Autosomal recessive hyper-IgE (immunoglobulin E) syndrome due to TYK2 deficiency", "TYK2 autosomal recessive mendelian susceptibility to mycobacterial diseases due to a partial deficiency", "autosomal recessive mendelian susceptibility to mycobacterial diseases due to a partial deficiency caused by mutation in TYK2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 35", "shortest_name_length": 5}
{"curie": "UMLS:C5206776", "names": ["Recurrent Dedifferentiated Chordoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Dedifferentiated Chordoma", "shortest_name_length": 35}
{"curie": "MONDO:0022552", "names": ["Bazopoulou Kyrkanidou syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bazopoulou Kyrkanidou syndrome", "shortest_name_length": 30}
{"curie": "MONDO:0001558", "names": ["Renal agenesis", "POTTER SYNDROME", "Potter sequence", "Potter Syndrome", "syndrome potter", "Potter syndrome", "potter syndrome", "syndrome; Potter", "Potter; syndrome", "potters syndrome", "Potter's Sequence", "potter's syndrome", "Potter's syndrome", "Potter's sequence", "Renofacial syndrome", "Renal agenesis syndrome", "Bilateral renal agenesis", "bilateral renal agenesis", "Oligohydramnios sequence", "Oligohydramnios Sequence", "oligohydramnios sequence", "Bilateral Renal Agenesis", "Hereditary renal agenesis", "Renal agenesis, bilateral", "Potter sequence (diagnosis)", "agenesis; kidney, bilateral", "Congenital absence of kidneys", "BRA - Bilateral renal agenesis", "absence; kidney(s), congenital", "Potter's anomaly of the kidney", "Urogenital adysplasia, hereditary", "Oligohydramnios sequence (disorder)", "Congenital absence of kidneys syndrome", "absence; kidney, congenital, bilateral", "Bilateral congenital absence of kidneys"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Potter sequence", "shortest_name_length": 14}
{"curie": "MONDO:0000684", "names": ["verbal auditory agnosia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "verbal auditory agnosia", "shortest_name_length": 23}
{"curie": "UMLS:C4551536", "names": ["Stage IIA Cervical Cancer", "FIGO Stage IIA Cervix Carcinoma", "Cervical Cancer Stage IIA AJCC v6", "AJCC Stage IIA Cervical Cancer v6", "Stage IIA Cervical Cancer AJCC v6", "FIGO Stage IIA Cervical Carcinoma", "FIGO Stage IIA Carcinoma of Cervix", "FIGO Stage IIA Cervix Uteri Carcinoma", "FIGO Stage IIA Carcinoma of the Cervix", "FIGO Stage IIA Uterine Cervix Carcinoma", "FIGO Stage IIA Carcinoma of Cervix Uteri", "FIGO Stage IIA Carcinoma of Uterine Cervix", "FIGO Stage IIA Carcinoma of the Cervix Uteri", "FIGO Stage IIA Carcinoma of the Uterine Cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Cervical Cancer AJCC v6", "shortest_name_length": 25}
{"curie": "UMLS:C1321897", "names": ["Stage 0 Penile Cancer", "Stage 0 Penile Cancer AJCC v6", "Stage 0 Penile Carcinoma AJCC v6", "Stage 0 Carcinoma of Penis AJCC v6", "Stage 0 Carcinoma of the Penis AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Penile Cancer AJCC v6", "shortest_name_length": 21}
{"curie": "UMLS:C5206798", "names": ["Advanced Gallbladder Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Gallbladder Carcinoma", "shortest_name_length": 30}
{"curie": "UMLS:C2826558", "names": ["Cystic Oncocytoma", "Cystic Oncocytic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cystic Oncocytic Neoplasm", "shortest_name_length": 17}
{"curie": "UMLS:C1518227", "names": ["Malignant Non-Hodgkin Lymphoma, Small Cleaved Cell", "Malignant Non-Hodgkin's Lymphoma, Small Cleaved Cell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Non-Hodgkin's Lymphoma, Small Cleaved Cell", "shortest_name_length": 50}
{"curie": "MONDO:0003343", "names": ["Retinal hemangioblastoma", "retinal hemangioblastoma", "Retinal Hemangioblastoma", "Retinal Capillary Hemangioma", "Retinal capillary hemangioma", "Capillary hemangioma of retina", "Capillary haemangioma of retina", "retinal capillary hemangioblastoma", "vasculature of retina hemangioblastoma", "hemangioblastoma of vasculature of retina", "Capillary hemangioma of retina (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal hemangioblastoma", "shortest_name_length": 24}
{"curie": "MONDO:0007959", "names": ["MDB", "CPNET", "CNS PNET", "Medulloblastoma", "MEDULLOBLASTOMA", "medulloblastoma", "Medulloblastomas", "medulloblastomas", "Medulloblastoma NOS", "Medulloblastoma, NOS", "CNS, medulloblastoma", "MDB - Medulloblastoma", "MDB - medulloblastoma", "brain medulloblastoma", "BRAIN, MEDULLOBLASTOMA", "medulloblastoma, somatic", "cerebellar medulloblastoma", "MEDULLOBLASTOMA, MALIGNANT", "medulloblastoma, malignant", "Medulloblastoma (disorder)", "medulloblastoma (diagnosis)", "medulloblastoma brain tumor", "brain medulloblastoma tumors", "BRAIN TUMOR, MEDULLOBLASTOMA", "medulloblastoma, Desmoplastic", "cerebellum embryonal neoplasm", "medulloblastoma of cerebellum", "neuroendocrine tumor medulloblastoma", "INTRACRANIAL NEOPLASM, MEDULLOBLASTOMA", "Medulloblastoma, histologically defined", "MEDULLOBLASTOMA PREDISPOSITION SYNDROME", "Medulloblastoma (morphologic abnormality)", "Localized Primitive Neuroectodermal Tumor", "medulloblastoma with extensive nodularity", "localized primitive neuroectodermal tumor", "medulloblastoma of cerebellum (diagnosis)", "infratentorial primitive neuroectodermal tumor", "central nervous system mass lesions cerebellum medulloblastoma", "medulloblastoma, autosomal recessive, autosomal dominant, somatic mutation", "medulloblastoma, desmoplastic, autosomal recessive, autosomal dominant, somatic mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "medulloblastoma", "shortest_name_length": 3}
{"curie": "MONDO:0006901", "names": ["peritoneum tumor", "peritoneum neoplasm", "tumor of peritoneum", "peritoneal neoplasm", "Tumor of peritoneum", "Peritoneal neoplasm", "Peritoneal Neoplasm", "Tumour of peritoneum", "Peritoneal Neoplasms", "Neoplasm, Peritoneal", "Abdominal wall tumor", "Abdominal wall tumour", "neoplasm of peritoneum", "Neoplasm of peritoneum", "Abdominal wall neoplasm", "Peritoneal neoplasm NOS", "Neoplasm of the peritoneum", "Neoplasm of abdominal wall", "Abdominal wall neoplasm NOS", "peritoneum neoplasm (disease)", "Neoplasm of peritoneum (disorder)", "neoplasm of peritoneum (diagnosis)", "Neoplasm of abdominal wall (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peritoneal neoplasm", "shortest_name_length": 16}
{"curie": "MONDO:0001408", "names": ["ischemic neuropathy", "Ischemic Neuropathy", "Ischemic neuropathy", "NEUROPATHY, ISCHEMIC", "Ischaemic neuropathy", "ischemic peripheral neuropathy", "Ischemic peripheral neuropathy", "Ischemic neuropathy (disorder)", "Ischaemic peripheral neuropathy", "Peripheral neuropathy, ischemic", "Ischemic peripheral neuropathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ischemic neuropathy", "shortest_name_length": 19}
{"curie": "MONDO:0003291", "names": ["Skin Leiomyoma", "skin leiomyoma", "leiomyoma cutis", "Leiomyoma Cutis", "Leiomyoma cutis", "leiomyoma of skin", "Leiomyoma of Skin", "cutaneous leiomyoma", "Cutaneous leiomyoma", "Cutaneous Leiomyoma", "Cutaneous leiomyomas", "Cutaneous leiomyomata", "leiomyoma of the skin", "Leiomyoma of the Skin", "zone of skin leiomyoma", "leiomyoma of zone of skin", "cutaneous (skin) leiomyoma", "Cutaneous (Skin) Leiomyoma", "Cutaneous leiomyoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leiomyoma cutis", "shortest_name_length": 14}
{"curie": "MONDO:0008720", "names": ["IAD", "ACTH deficiency", "ACTH Deficiency", "deficiency; ACTH", "ACTH; deficiency", "Corticotropin Deficiency", "Secondary hypoadrenalism", "Isolated ACTH deficiency", "Secondary Hypoadrenalism", "Corticotropin deficiency", "isolated ACTH deficiency", "ACTH deficiency, isolated", "ACTH Deficiency, Isolated", "Corticotrophin deficiency", "secretion; ACTH deficient", "ACTH DEFICIENCY, ISOLATED", "Secondary Adrenal Insufficiency", "Isolated corticotropin deficiency", "Specific corticotropin deficiency", "congenital isolated ACTH deficiency", "Adrenocorticotropic Hormone Deficiency", "ADRENOCORTICOTROPIC HORMONE DEFICIENCY", "Adrenocorticotropic hormone deficiency", "adrenocorticotropic hormone deficiency", "Isolated corticotropin deficiency (disorder)", "Adrenocorticotropic hormone (ACTH) deficiency", "Isolated adrenocorticotropic hormone deficiency", "isolated adrenocorticotropic hormone deficiency", "Adrenocorticotropic hormone deficiency (disorder)", "Adrenocorticotropic hormone (ACTH) deficiency (disorder)", "congenital isolated adrenocorticotropic hormone deficiency", "congenital isolated adrenocorticotropic hormone deficiency (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital isolated adrenocorticotropic hormone deficiency", "shortest_name_length": 3}
{"curie": "MONDO:0007346", "names": ["Cochleosaccular Degeneration", "cochleosaccular degeneration-cataract syndrome", "Cochleosaccular degeneration-cataract syndrome", "Cochleosaccular degeneration and cataract syndrome", "Cochleosaccular degeneration with progressive cataract", "COCHLEOSACCULAR degeneration with progressive cataracts", "COCHLEOSACCULAR DEGENERATION WITH PROGRESSIVE CATARACTS", "Cochleosaccular degeneration and cataract syndrome (disorder)", "Cochleosaccular degeneration of the inner ear and progressive cataracts", "Cochleosaccular Degeneration of the Inner Ear with Progressive Cataracts", "Cochleosaccular Degeneration of the inner Ear with progressive cataracts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cochleosaccular degeneration-cataract syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0017104", "names": ["central nervous system cystic malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system cystic malformation", "shortest_name_length": 42}
{"curie": "MONDO:0003590", "names": ["Fibroblastic Liposarcoma", "Fibroblastic liposarcoma", "fibroblastic liposarcoma", "fibroblastic liposarcoma (diagnosis)", "Fibroblastic liposarcoma (morphologic abnormality)", "fibroblastic liposarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibroblastic liposarcoma", "shortest_name_length": 24}
{"curie": "MONDO:0012803", "names": ["Trehalase Deficiency", "Trehalase deficiency", "TREHALASE DEFICIENCY", "trehalase deficiency", "trehalose intolerance", "Trehalose Intolerance", "Trehalose intolerance", "TREHALOSE INTOLERANCE", "isolated trehalose intolerance", "Isolated trehalose intolerance", "Trehalase deficiency (disorder)", "alpha, alpha-Trehalase deficiency", "Alpha, alpha-trehalase deficiency", "diarrhea-vomiting due to trehalase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diarrhea-vomiting due to trehalase deficiency", "shortest_name_length": 20}
{"curie": "UMLS:C0948393", "names": ["Edematous pancreatitis", "edematous; pancreatitis", "Oedematous pancreatitis", "pancreatitis; edematous"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Edematous pancreatitis", "shortest_name_length": 22}
{"curie": "UMLS:C5237256", "names": ["Shared Neoantigen-Positive Malignant Solid Tumor", "Shared Neoantigen-Positive Malignant Solid Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Shared Neoantigen-Positive Malignant Solid Neoplasm", "shortest_name_length": 48}
{"curie": "UMLS:C1305147", "names": ["Supravalvar aortic stenosis", "SVAS - Supravalvar aortic stenosis", "Congenital supravalvular aortic stenosis", "congenital supravalvular aortic stenosis", "supravalvular; aorta stenosis, congenital", "stenosis; aorta, congenital, supravalvular", "aorta; stricture, supravalvular, congenital", "Congenital supravalvular aortic stenosis (disorder)", "congenital supravalvular aortic stenosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital supravalvular aortic stenosis", "shortest_name_length": 27}
{"curie": "MONDO:0010758", "names": ["MCS", "WRWF", "MRXS4", "WRWFXLR", "WIEACKER SYNDROME", "Wieacker syndrome", "Wieacker Wolff syndrome", "Wieacker-Wolff Syndrome", "Wieacker-Wolff syndrome", "WIEACKER-WOLFF SYNDROME", "Miles-Carpenter syndrome", "Wieacker-Wolff syndrome, X-linked", "mental retardation, X-linked, syndromic 4", "MENTAL RETARDATION, X-LINKED, SYNDROMIC 4", "Mental retardation, X-linked, syndromic 4", "Wieacker-Wolff syndrome, X-linked recessive", "Miles-CARPENTER X-linked mental retardation syndrome", "Miles-Carpenter x-linked mental retardation syndrome", "MILES-CARPENTER X-LINKED MENTAL RETARDATION SYNDROME", "X-linked intellectual disability Miles-Carpenter type", "X-linked intellectual disability Miles Carpenter type", "X-linked intellectual disability, Miles-Carpenter type", "contractures-muscle atrophy-oculomotor apraxia syndrome", "apraxia-oculomotor contractures-muscle atrophy syndrome", "muscle atrophy-contractures-oculomotor apraxia syndrome", "contractures of feet, muscle atrophy, and oculomotor apraxia", "Contractures of feet, muscle atrophy, and oculomotor apraxia", "Foot contractures-muscle atrophy-oculomotor apraxia syndrome", "MILES-CARPENTER X-LINKED INTELLECTUAL DEVELOPMENTAL DISORDER", "CONTRACTURES OF FEET, MUSCLE ATROPHY, AND OCULOMOTOR APRAXIA", "foot contractures-muscle atrophy-oculomotor apraxia syndrome", "Foot contracture, muscle atrophy, oculomotor apraxia syndrome", "X-linked intellectual disability Miles Carpenter type (disorder)", "X-linked intellectual disability Miles Carpenter type (diagnosis)", "intellectual disability-developmental delay-contractures syndrome", "Intellectual disability-developmental delay-contractures syndrome", "intellectual disability, developmental delay, contracture syndrome", "Intellectual disability, developmental delay, contracture syndrome", "APRAXIA, OCULOMOTOR, WITH CONGENITAL CONTRACTURES AND MUSCLE ATROPHY", "apraxia, oculomotor, with congenital contractures and muscle atrophy", "Apraxia, oculomotor, with congenital contractures and muscle atrophy", "Intellectual disability, developmental delay, contracture syndrome (disorder)", "intellectual disability, developmental delay, contracture syndrome (diagnosis)", "MENTAL RETARDATION, X-LINKED, WITH CONGENITAL CONTRACTURES AND LOW FINGERTIP ARCHES", "mental retardation, X-linked, with congenital contractures and Low fingertip arches", "mental retardation, X-linked, with congenital contractures and low fingertip arches", "Mental Retardation, X-Linked, with Congenital Contractures and Low Fingertip Arches"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wieacker-Wolff syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0012972", "names": ["FEB10", "familial febrile seizures 10", "FEBRILE SEIZURES, FAMILIAL, 10", "febrile seizures, familial, 10", "Seizures, Familial Febrile, 10", "familial febrile convulsions 10", "CONVULSIONS, FAMILIAL FEBRILE, 10", "convulsions, familial febrile, 10", "Febrile Convulsions, Familial, 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "febrile seizures, familial, 10", "shortest_name_length": 5}
{"curie": "UMLS:C5239594", "names": ["Primary Peritoneal Endometrioid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Peritoneal Endometrioid Adenocarcinoma", "shortest_name_length": 46}
{"curie": "MONDO:0009542", "names": ["Lysine Malabsorption Syndrome", "lysine malabsorption syndrome", "LYSINE MALABSORPTION SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lysine malabsorption syndrome", "shortest_name_length": 29}
{"curie": "MONDO:0012409", "names": ["MCOP2", "isolated microphthalmia 2", "microphthalmia, isolated 2", "Microphthalmia, Isolated 2", "MICROPHTHALMIA, ISOLATED 2", "VSX2 isolated microphthalmia", "isolated microphthalmia type 2", "microphthalmia, isolated type 2", "ANOPHTHALMIA, CLINICAL, ISOLATED", "anophthalmia, clinical, isolated", "isolated microphthalmia caused by mutation in VSX2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated microphthalmia 2", "shortest_name_length": 5}
{"curie": "MONDO:0015240", "names": ["DA1", "DA1A", "AMCD1", "DIGITOTALAR DYSMORPHISM", "ULNAR DRIFT, HEREDITARY", "Digitotalar dysmorphism", "Ulnar Drift, Hereditary", "digitotalar dysmorphism", "Digitotalar Dysmorphism", "Distal arthrogryposis type 1", "arthrogryposis distal type 1", "distal arthrogryposis type 1", "Distal Arthrogryposis Type 1", "Distal arthrogryposis, type 1", "distal type 1A arthrogryposis", "Arthrogryposis, distal, type 1", "ARTHROGRYPOSIS, DISTAL, TYPE 1", "ARTHROGRYPOSIS, DISTAL, TYPE 1A", "Distal arthrogryposis type 1 (disorder)", "distal arthrogryposis type 1A (sub-type)", "distal arthrogryposis type 1B (sub-type)", "distal type 1A arthrogryposis (diagnosis)", "arthrogryposis multiplex congenita distal type 1", "Arthrogryposis multiplex congenita, distal type 1", "Arthrogryposis Multiplex Congenita, Distal, Type I", "ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "digitotalar dysmorphism", "shortest_name_length": 3}
{"curie": "UMLS:C4288775", "names": ["Malignant Cervical Soft Tissue Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Cervical Soft Tissue Neoplasm", "shortest_name_length": 39}
{"curie": "UMLS:C0340952", "names": ["secondary anemia", "Secondary anemia", "SECONDARY ANEMIA", "anemia secondary", "Secondary anaemia", "Anemia, secondary", "SECONDARY ANAEMIA", "Secondary anemia NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary anemia NOS", "shortest_name_length": 16}
{"curie": "UMLS:C1335022", "names": ["Non-Neoplastic Sinonasal Disorder", "Non-Neoplastic Nasal Cavity and Paranasal Sinus Disease", "Non-Neoplastic Nasal Cavity and Paranasal Sinus Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Sinonasal Disorder", "shortest_name_length": 33}
{"curie": "MONDO:0700011", "names": ["chromosome 4 disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 4 disorder", "shortest_name_length": 21}
{"curie": "MONDO:0015521", "names": ["juvenile or adult CACH syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile or adult CACH syndrome", "shortest_name_length": 31}
{"curie": "UMLS:C4551765", "names": ["Stage III Cervical Cancer", "Cervical Cancer Stage III", "Cervical Carcinoma Stage III", "stage III cancer of the cervix", "FIGO Stage III Cervix Carcinoma", "Stage III Cervical Cancer AJCC v6", "FIGO Stage III Cervical Carcinoma", "Stage III Cervical Cancer AJCC v7", "FIGO Stage III Carcinoma of Cervix", "FIGO Stage III Cervix Uteri Carcinoma", "FIGO Stage III Carcinoma of the Cervix", "FIGO Stage III Uterine Cervix Carcinoma", "FIGO Stage III Carcinoma of Cervix Uteri", "Stage III Cervical Cancer AJCC v6 and v7", "FIGO Stage III Carcinoma of Uterine Cervix", "FIGO Stage III Carcinoma of the Cervix Uteri", "FIGO Stage III Carcinoma of the Uterine Cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Cervical Cancer AJCC v6 and v7", "shortest_name_length": 25}
{"curie": "MONDO:0014299", "names": ["SWNTS2", "SCHWANNOMATOSIS 2", "schwannomatosis 2", "Schwannomatosis type 2", "schwannomatosis-2, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schwannomatosis 2", "shortest_name_length": 6}
{"curie": "UMLS:C5420399", "names": ["Recurrent Ectomesenchymoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Ectomesenchymoma", "shortest_name_length": 26}
{"curie": "MONDO:0014662", "names": ["HSAN8", "HSAN 8", "HSAN VIII", "CIP-hypohidrosis syndrome", "hereditary sensory and autonomic neuropathy type 8", "Hereditary sensory and autonomic neuropathy type 8", "neuropathy, hereditary sensory and autonomic, type 8", "Hereditary sensory and autonomic neuropathy type VIII", "hereditary sensory and autonomic neuropathy type VIII", "congenital insensitivity to pain-hypohidrosis syndrome", "neuropathy, hereditary sensory and autonomic, type VIII", "NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VIII", "HSAN8 - hereditary sensory and autonomic neuropathy type 8", "Hereditary sensory and autonomic neuropathy type 8 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital insensitivity to pain-hypohidrosis syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0019020", "names": ["PANDAS", "PANDAS (diagnosis)", "personality disorder pandas", "Pediatric autoimmune disorders associated with Streptococcus infections", "pediatric autoimmune disorders associated with Streptococcus infections", "pediatric autoimmune neuropsychiatric disorder associated with Streptococcus", "Pediatric autoimmune neuropsychiatric disorder associated with streptococcal infection", "Pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection", "Paediatric autoimmune neuropsychiatric disorder associated with streptococcal infection", "Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcal infections", "Paediatric autoimmune neuropsychiatric disorders associated with streptococcal infection", "Pediatric autoimmune neuropsychiatric disorders associated with Streptococcus infections", "Pediatric autoimmune neuropsychiatric disorders associated with streptococcal infections", "pediatric autoimmune neuropsychiatric disorders associated with Streptococcus infections", "pediatric autoimmune neuropsychiatric disorders associated with streptococcal infections", "PANDAS - Pediatric autoimmune neuropsychiatric disorder associated with streptococcal infection", "PANDAS Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcal infections", "PANDAS - Paediatric autoimmune neuropsychiatric disorder associated with streptococcal infection", "Pediatric autoimmune neuropsychiatric disorder associated with streptococcal infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PANDAS", "shortest_name_length": 6}
{"curie": "MONDO:0019508", "names": ["PIT", "VWS", "LPS", "VDWS", "Van der Woude", "lip pit syndrome", "Lip-pit syndrome", "LIP-PIT SYNDROME", "Lip-Pit Syndrome", "lip-pit syndrome", "Lip pit syndrome", "Van der Woude Syndrome", "van der Woude syndrome", "Van der Woude syndrome", "van der woude syndrome", "Van Der Woude Syndrome", "der syndrome van woudes", "van der woude's syndrome", "Van der Woude's syndrome", "Lip-pit-cleft lip syndrome", "Lip-pit, cleft lip syndrome", "Van der Woude syndrome (disorder)", "Van der Woude syndrome (diagnosis)", "Cleft lip/palate with mucous cysts of lower lip", "cleft lip/palate with mucous cysts of lower lip", "CLEFT LIP AND/OR PALATE WITH MUCOUS CYSTS OF LOWER LIP", "cleft lip and/or palate with mucous cysts of lower lip", "Cleft lip and-or palate with mucous cysts of lower lip"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "van der Woude syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C2981709", "names": ["IIIB", "Stage IIIB Uveal Melanoma", "Stage IIIB Uveal Melanoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Uveal Melanoma AJCC v7", "shortest_name_length": 4}
{"curie": "MONDO:0008562", "names": ["Thumb Deformity And Alopecia", "THUMB DEFORMITY AND ALOPECIA", "thumb deformity and alopecia", "Thumb deformity, alopecia, pigmentation anomaly", "thumb deformity, alopecia, pigmentation anomaly", "thumb deformity-alopecia-pigmentation anomaly syndrome", "Congenital deformity of the thumb and congenital alopecia", "congenital deformity of the thumb and congenital alopecia", "Hypotrichosis associated with congenital hypoplasia of the thumb", "hypotrichosis associated with congenital hypoplasia of the thumb", "sparse hair, short stature, hypoplastic thumbs, single upper central incisor and abnormal skin pigmentation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thumb deformity-alopecia-pigmentation anomaly syndrome", "shortest_name_length": 28}
{"curie": "UMLS:C0859086", "names": ["Malignant Nipple Tumor", "Malignant Nipple Neoplasm", "Malignant nipple neoplasm", "Malignant Tumor of Nipple", "Malignant Neoplasm of Nipple", "Malignant nipple neoplasm NOS", "Malignant Tumor of the Nipple", "Malignant Neoplasm of the Nipple"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant nipple neoplasm", "shortest_name_length": 22}
{"curie": "UMLS:C4551545", "names": ["Stage III", "Stage III Cancer of Testis", "Stage III Testicular Cancer", "stage III testicular cancer", "Stage III Cancer of the Testis", "Stage III Testicular Cancer AJCC v6", "Stage III Testicular Cancer AJCC v7", "Stage III Testicular Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Testicular Cancer AJCC v6 and v7", "shortest_name_length": 9}
{"curie": "MONDO:0100380", "names": ["AML, t(4;11)(q21;q23)", "AML, t(4;11)(q21;q23.3)", "acute myeloid leukemia, t(4;11)(q21;q23)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, t(4;11)(q21;q23)", "shortest_name_length": 21}
{"curie": "MONDO:0023283", "names": ["GCT of the ovary", "ovary granulosa cell tumor", "Granulosa theca cell tumor", "cell granulosa ovary tumor", "granulosa theca cell tumor", "OVARY, GRANULOSA CELL TUMOR", "ovarian granulosa cell tumor", "Ovarian granulosa cell tumor", "Ovarian Granulosa Cell Tumor", "Ovarian granulosa cell tumour", "Granulosa Cell Tumor of Ovary", "granulosa cell tumor of ovary", "Granulosa cell tumor of ovary", "Granulosa cell tumour of ovary", "ovarian granulosa cell neoplasm", "Ovarian Granulosa Cell Neoplasm", "Granulosa Cell Neoplasm of Ovary", "granulosa cell neoplasm of ovary", "Granulosa cell tumor of the ovary", "Granulosa Cell Tumor of the Ovary", "granulosa cell tumor of the ovary", "OVARY, SEX CHORD-MESENCHYMAL TUMOR", "granulosa cell neoplasm of the ovary", "Granulosa Cell Neoplasm of the Ovary", "OVARIAN CANCER, SEX CHORD-MESENCHYMAL", "adult granulosa cell tumor of the ovary", "granulosa theca cell tumor of the ovary", "Granulosa theca cell tumor of the ovary", "Adult granulosa cell tumor of the ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian granulosa cell tumor", "shortest_name_length": 16}
{"curie": "MONDO:0010178", "names": ["CAVD", "CBAVD", "CUAVD", "congenital bilateral absence of vas deferens", "vas deferens, congenital bilateral aplasia of", "VAS DEFERENS, CONGENITAL UNILATERAL APLASIA OF", "congenital bilateral aplasia of the vas deferens", "Congenital Bilateral Aplasia of the Vas Deferens", "congenital bilateral aplasia of vas deferens from CFTR mutation", "autosomal recessive congenital bilateral absence of vas deferens"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital bilateral aplasia of vas deferens from CFTR mutation", "shortest_name_length": 4}
{"curie": "UMLS:C1855792", "names": ["Nonbullous congenital ichthyosiform erythroderma 1", "Ichthyosiform Erythroderma, Congenital, Nonbullous, 1", "ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL, NONBULLOUS, 1", "Ichthyosiform erythroderma, Brocq congenital, nonbullous form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL, NONBULLOUS, 1", "shortest_name_length": 50}
{"curie": "MONDO:0019794", "names": ["ADCA4", "ADCAIV", "autosomal dominant cerebellar ataxia type 4", "autosomal dominant cerebellar ataxia type IV"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant cerebellar ataxia type IV", "shortest_name_length": 5}
{"curie": "MONDO:0012427", "names": ["AAT3", "LDS2", "MFS2", "Marfan Syndrome Type 2", "Loeys-Dietz syndrome 2", "LOEYS-DIETZ SYNDROME 2", "Marfan syndrome type 2", "Marfan Syndrome Type II", "Marfan syndrome type II", "Marfan Syndrome, Type II", "Marfan syndrome, type II", "Loeys-Dietz syndrome type 2", "Loeys-Dietz Syndrome Type 2", "TGFBR2 Loeys-Dietz syndrome", "Loeys-Dietz syndrome type 2b", "Loeys-Dietz syndrome type II", "Loeys-Dietz Syndrome Type II", "Loeys-Dietz Syndrome, Type 2b", "MARFAN SYNDROME, TYPE II, FORMERLY", "Marfan syndrome, type II, formerly", "familial throacic aortic aneurysm 3", "Aortic aneurysm, familial thoracic 3", "aortic aneurysm, familial thoracic 3", "AORTIC ANEURYSM, FAMILIAL THORACIC 3", "Marfan Like Connective Tissue Disorder", "Loeys-Dietz syndrome type 2b (diagnosis)", "Loeys-Dietz syndrome caused by mutation in TGFBR2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Loeys-Dietz syndrome 2", "shortest_name_length": 4}
{"curie": "MONDO:0005576", "names": ["Cryoglobulinemia", "cryoglobulinemia", "CRYOGLOBULINEMIA", "Cryoglobulinemias", "Cryoglobulinaemia", "cryoglobulinemias", "CRYOGLOBULINAEMIA", "cryoglobulinaemia", "Cryoglobulinemia, NOS", "Cryoglobulinaemia, NOS", "Cryoimmunoglobulinemia", "Cryoimmunoglobulinaemia", "Cryoglobulinemia (disorder)", "Cryoimmunoglobulinemia, NOS", "cryoglobulinemia (diagnosis)", "Cryoprecipitable immune complexes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cryoglobulinemia", "shortest_name_length": 16}
{"curie": "MONDO:0100014", "names": ["AIR", "Autoimmune retinopathy", "autoimmune retinopathy", "retina autoimmune disease", "autoimmune disease of retina", "Autoimmune retinopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune retinopathy", "shortest_name_length": 3}
{"curie": "UMLS:C1142492", "names": ["Postinfarction angina"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postinfarction angina", "shortest_name_length": 21}
{"curie": "MONDO:0014557", "names": ["AOA4", "ATAXIA-OCULOMOTOR APRAXIA 4", "ataxia-oculomotor apraxia 4", "ataxia-oculomotor apraxia-4", "Ataxia-oculomotor apraxia type 4", "ataxia - oculomotor apraxia type 4", "PNKP oculomotor apraxia or related oculomotor disease", "oculomotor apraxia or related oculomotor disease caused by mutation in PNKP"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ataxia - oculomotor apraxia type 4", "shortest_name_length": 4}
{"curie": "MONDO:0011422", "names": ["AR pRTA", "RTA, proximal, autosomal recessive", "RTA, PROXIMAL, AUTOSOMAL RECESSIVE", "Rta, Proximal, Autosomal Recessive", "autosomal recessive proximal renal tubular acidosis", "Autosomal recessive proximal renal tubular acidosis", "proximal renal tubular acidosis, autosomal recessive", "renal tubular acidosis, proximal, with ocular abnormalities", "Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation", "RENAL TUBULAR ACIDOSIS, PROXIMAL, WITH OCULAR ABNORMALITIES AND MENTAL RETARDATION", "renal tubular acidosis, proximal, with ocular abnormalities and mental retardation", "Proximal renal tubular acidosis with ocular abnormalities and intellectual disability", "proximal renal tubular acidosis with ocular abnormalities and intellectual disability", "renal tubular acidosis, proximal, with ocular abnormalities and intellectual disability", "RENAL TUBULAR ACIDOSIS, PROXIMAL, WITH OCULAR ABNORMALITIES AND IMPAIRED INTELLECTUAL DEVELOPMENT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive proximal renal tubular acidosis", "shortest_name_length": 7}
{"curie": "MONDO:0012689", "names": ["POF5", "Pof5", "Premature Ovarian Failure 5", "PREMATURE OVARIAN FAILURE 5", "premature ovarian failure 5", "NOBOX primary ovarian failure", "primary ovarian insufficiency 5", "premature ovarian failure type 5", "primary ovarian failure caused by mutation in NOBOX"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "premature ovarian failure 5", "shortest_name_length": 4}
{"curie": "MONDO:0020847", "names": ["MRD58", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 58", "MENTAL RETARDATION, autosomal dominant 58", "intellectual disability, autosomal dominant 58", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 58"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 58", "shortest_name_length": 5}
{"curie": "UMLS:C2983570", "names": ["Bladder Cancer by AJCC v6 Stage", "Bladder Carcinoma by AJCC v6 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder Cancer by AJCC v6 Stage", "shortest_name_length": 31}
{"curie": "UMLS:C0004615", "names": ["Bacterial Infections and Mycoses"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bacterial Infections and Mycoses", "shortest_name_length": 32}
{"curie": "UMLS:C5205067", "names": ["Refractory Transformed Follicular Lymphoma to Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Transformed Follicular Lymphoma to Diffuse Large B-Cell Lymphoma", "shortest_name_length": 75}
{"curie": "MONDO:0006996", "names": ["thyroid storm", "THYROID STORM", "Thyroid storm", "storm thyroid", "Thyroid Storm", "Storm, Thyroid", "crisis thyroid", "Thyroid Crisis", "Thyroid crisis", "THYROID CRISIS", "thyroid storms", "Crisis thyroid", "CRISIS THYROID", "thyroid crisis", "crisis; thyroid", "thyroid; crisis", "Crisis, Thyroid", "thyrotoxic storm", "Thyrotoxic Storm", "THYROTOXIC STORM", "Thyrotoxic Crisis", "thyrotoxic crisis", "Storm, Thyrotoxic", "Thyrotoxic crisis", "THYROTOXIC CRISIS", "thyrotoxic crises", "storm; thyrotoxic", "thyrotoxic; storm", "crisis; thyrotoxic", "thyrotoxic; crisis", "Crisis, Thyrotoxic", "thyroid crisis (storm)", "Thyroid crisis or storm", "thyroid crisis (disease)", "Hyperthyroidism with Storm", "Thyrotoxic crisis (disorder)", "Thyrotoxic crisis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid crisis", "shortest_name_length": 13}
{"curie": "UMLS:C4525042", "names": ["Stage III Appendix Cancer", "Stage III Appendix Carcinoma AJCC v8", "Stage III Appendiceal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Appendix Carcinoma AJCC v8", "shortest_name_length": 25}
{"curie": "MONDO:0010847", "names": ["SCA4", "Spinocerebellar Ataxias", "Spinocerebellar atrophy", "spinocerebellar ataxia 4", "Spinocerebellar Ataxia 4", "Spinocerebellar Ataxia-4", "SPINOCEREBELLAR ATAXIA 4", "Ataxia 4, Spinocerebellar", "Spinocerebellar Ataxia 4s", "Spinocerebellar ataxia type 4", "spinocerebellar ataxia type 4", "Type 4 Spinocerebellar Ataxia", "Spinocerebellar Ataxia Type 4", "Spinocerebellar ataxia type 4 (disorder)", "spinocerebellar ataxia autosomal dominant with sensory axonal neuropathy", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL DOMINANT, WITH SENSORY AXONAL NEUROPATHY", "Spinocerebellar Ataxia, Autosomal Dominant, with Sensory Axonal Neuropathy", "spinocerebellar ataxia, autosomal dominant, with sensory axonal neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia type 4", "shortest_name_length": 4}
{"curie": "MONDO:0006416", "names": ["small intestine Burkitt lymphoma", "Small Intestine Burkitt Lymphoma", "small intestinal Burkitt lymphoma", "small intestine Burkitts lymphoma", "Small Intestinal Burkitt Lymphoma", "Small Intestine Burkitt's Lymphoma", "small intestine Burkitt's lymphoma", "Small Intestinal Burkitt's Lymphoma", "Burkitt lymphoma of small intestine", "small intestinal Burkitt's lymphoma", "Burkitts lymphoma of small intestine", "Burkitt's lymphoma of small intestine", "primary small intestinal Burkitt's lymphoma", "Primary Small Intestinal Burkitt's Lymphoma", "Burkitt's lymphoma of small intestine (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small intestinal Burkitt lymphoma", "shortest_name_length": 32}
{"curie": "MONDO:0015205", "names": ["Isolated lissencephaly type 1 without known genetic defect", "isolated lissencephaly type 1 without known genetic defects", "Isolated lissencephaly type 1 without known genetic defects", "Isolated lissencephaly type 1 without known genetic defect (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated lissencephaly type 1 without known genetic defects", "shortest_name_length": 58}
{"curie": "MONDO:0700135", "names": ["Bovine Leukemia", "bovine leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bovine leukemia", "shortest_name_length": 15}
{"curie": "MONDO:0016948", "names": ["partial trisomy of chromosome 11p", "partial duplication of chromosome 11p", "partial trisomy of the short arm of chromosome 11", "partial duplication of the short arm of chromosome 11", "partial duplication of the short arm of chromosome type 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of the short arm of chromosome 11", "shortest_name_length": 33}
{"curie": "MONDO:0009612", "names": ["MCM deficiency", "MMA due to MCM Deficiency", "MMA DUE TO MCM DEFICIENCY", "methylmalonic aciduria mut type", "METHYLMALONIC ACIDURIA, mut TYPE", "Methylmalonic Aciduria, Mut Type", "Methylmalonic Aciduria, MUT Type", "methylmalonic aciduria, mut type", "Methylmalonic Aciduria, mut(-) Type", "METHYLMALONIC ACIDURIA, mut(-) TYPE", "methylmalonic aciduria, mut(-) type", "Methylmalonic Aciduria, mut(0) Type", "METHYLMALONIC ACIDURIA, mut(0) TYPE", "methylmalonyl-CoA mutase deficiency", "methylmalonic aciduria, mut(0) type", "methylmalonyl-Coenzyme A mutase deficiency", "vitamin B12-unresponsive methylmalonic acidemia", "vitamin B12-unresponsive methylmalonic aciduria", "METHYLMALONIC ACIDEMIA DUE TO METHYLMALONYL-CoA MUTASE DEFICIENCY", "METHYLMALONIC ACIDURIA DUE TO METHYLMALONYL-CoA MUTASE DEFICIENCY", "Methylmalonic Acidemia due to Methylmalonyl-CoA Mutase Deficiency", "methylmalonic acidemia due to methylmalonyl-CoA mutase deficiency", "Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency", "methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency", "Methylmalonic Aciduria Due to Methylmalonyl-CoA Mutase Deficiency", "methylmalonic acidemia due to methylmalonyl-Coa mutase deficiency MMA due to MCM deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency", "shortest_name_length": 14}
{"curie": "UMLS:C0152515", "names": ["Intestinal infection due to pseudomonas", "Intestinal infection due to Pseudomonas", "Intestinal infection caused by Pseudomonas", "Intestinal infection due to Pseudomonas (diagnosis)", "Intestinal infection caused by Pseudomonas (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal infection due to Pseudomonas", "shortest_name_length": 39}
{"curie": "MONDO:0002972", "names": ["posterior mediastinum cancer", "Cancer of posterior mediastinum", "cancer of posterior mediastinum", "malignant posterior mediastinum neoplasm", "malignant tumor of posterior of mediastinum", "malignant neoplasm of posterior mediastinum", "Malignant neoplasm of posterior mediastinum", "malignant neoplasm of posterior of mediastinum", "Malignant neoplasm of posterior mediastinum (disorder)", "malignant neoplasm of posterior of mediastinum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "posterior mediastinum cancer", "shortest_name_length": 28}
{"curie": "MONDO:0002601", "names": ["teratoma", "Teratoma", "TERATOMA", "teratomas", "Teratomas", "Dysembryoma", "Teratoma NOS", "Dysembryomas", "Teratoma, NOS", "Teratoid Tumor", "teratoid tumor", "Tumor, Teratoid", "teratoid tumors", "Teratoid Tumors", "Tumors, Teratoid", "Teratoma (disorder)", "teratoma (diagnosis)", "Teratoma, Not Otherwise Specified", "Teratoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "teratoma", "shortest_name_length": 8}
{"curie": "MONDO:0009513", "names": ["LOCS", "JEB2C", "LOC syndrome", "LOGIC SYNDROME", "logic syndrome", "LOGIC syndrome", "Logic syndrome", "Shabbir syndrome", "LARYNGOONYCHOCUTANEOUS SYNDROME", "LARYNGOONYCHOCUTANEOUS syndrome", "Laryngoonychocutaneous Syndrome", "Laryngoonychocutaneous syndrome", "Laryngo-onychocutaneous syndrome", "laryngo-onycho-cutaneous syndrome", "Laryngo-onycho-cutaneous syndrome", "Laryngo onycho cutaneous syndrome", "Laryngo-onycho-cutaneous syndrome (disorder)", "Laryngeal and ocular granulation in indian children", "EPIDERMOLYSIS BULLOSA, JUNCTIONAL 2C, LARYNGOONYCHOCUTANEOUS", "laryngeal and ocular granulation tissue in children from the Indian subcontinent syndrome", "Laryngeal and ocular granulation tissue in children from the Indian subcontinent syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laryngo-onycho-cutaneous syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0012218", "names": ["ADDWOC", "DANDY-WALKER MALFORMATION WITH OCCIPITAL CEPHALOCELE, AUTOSOMAL DOMINANT", "Dandy-Walker malformation with occipital cephalocele, autosomal dominant", "Dandy-Walker Malformation With Occipital Cephalocele, Autosomal Dominant", "dandy-walker malformation with occipital cephalocele, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dandy-walker malformation with occipital cephalocele, autosomal dominant", "shortest_name_length": 6}
{"curie": "UMLS:C4551763", "names": ["Cervical Cancer Stage I", "Stage I Cervical Cancer", "Cervical Carcinoma Stage I", "stage I cancer of the cervix", "AJCC Stage I Cervical Cancer", "FIGO Stage I Cervix Carcinoma", "Uterine Cervix Cancer Stage I", "FIGO Stage I Cervical Carcinoma", "Stage I Cervical Cancer AJCC v6", "Stage I Cervical Cancer AJCC v7", "FIGO Stage I Carcinoma of Cervix", "FIGO Stage I Cervix Uteri Carcinoma", "FIGO Stage I Carcinoma of the Cervix", "FIGO Stage I Uterine Cervix Carcinoma", "FIGO Stage I Carcinoma of Cervix Uteri", "Stage I Cervical Cancer AJCC v6 and v7", "FIGO Stage I Carcinoma of Uterine Cervix", "FIGO Stage I Carcinoma of the Cervix Uteri", "FIGO Stage I Carcinoma of the Uterine Cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Cervical Cancer AJCC v6 and v7", "shortest_name_length": 23}
{"curie": "MONDO:0007423", "names": ["Deafness, Mid-Tone Neural", "deafness, mid-tone neural", "DEAFNESS, MID-TONE NEURAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness, mid-tone neural", "shortest_name_length": 25}
{"curie": "MONDO:0017148", "names": ["HpaH", "FPAH", "HPAH", "familial pulmonary arterial hypertension", "heritable pulmonary arterial hypertension", "Heritable Pulmonary Arterial Hypertension", "hereditary pulmonary arterial hypertension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heritable pulmonary arterial hypertension", "shortest_name_length": 4}
{"curie": "UMLS:C1698768", "names": ["mucositis of larynx", "Laryngeal Mucositis", "Laryngeal mucositis", "mucositis of larynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laryngeal Mucositis", "shortest_name_length": 19}
{"curie": "UMLS:C2931037", "names": ["Pancreatic cancer, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic cancer, adult", "shortest_name_length": 24}
{"curie": "UMLS:C1112341", "names": ["connective tissue inflammation", "Connective tissue inflammation", "connective tissue; inflammation", "inflammation; connective tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Connective tissue inflammation", "shortest_name_length": 30}
{"curie": "MONDO:0001015", "names": ["Eosinophilic meningitis", "Meningitis eosinophilic", "eosinophilic meningitis", "Eosinophilic Meningitis", "MENINGITIS, EOSINOPHILIC", "Chronic eosinophilic meningitis", "Eosinophilic meningitis (disorder)", "eosinophilic meningitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eosinophilic meningitis", "shortest_name_length": 23}
{"curie": "UMLS:C0751952", "names": ["Anterior Circulation Brain Infarction", "Anterior Circulation Infarction, Brain", "Brain Infarction, Anterior Circulation", "Infarction, Brain, Anterior Circulation", "Infarction, Anterior Circulation, Brain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anterior Circulation Brain Infarction", "shortest_name_length": 37}
{"curie": "UMLS:C1336011", "names": ["SLL with IGVH SH", "Postgerminal Center Small Lymphocytic Lymphoma", "Small Lymphocytic Lymphoma with Immunoglobulin Heavy Chain Variable-Region Gene Somatic Hypermutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Lymphocytic Lymphoma with Immunoglobulin Heavy Chain Variable-Region Gene Somatic Hypermutation", "shortest_name_length": 16}
{"curie": "UMLS:C2981380", "names": ["Stage IIIA Small Intestinal Cancer", "Stage IIIA Small Intestinal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Small Intestinal Cancer AJCC v7", "shortest_name_length": 34}
{"curie": "MONDO:0023153", "names": ["Tuberculous Ascites", "Tuberculous ascites", "tuberculous ascites", "ascites; tuberculous", "Tuberculous ascites (disorder)", "tuberculous ascites (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tuberculous ascites", "shortest_name_length": 19}
{"curie": "UMLS:C4725830", "names": ["Prostate Adenocarcinoma without Neuroendocrine Differentiation", "Prostate Adenocarcinoma without Evidence of Neuroendocrine Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Adenocarcinoma without Neuroendocrine Differentiation", "shortest_name_length": 62}
{"curie": "UMLS:C1265956", "names": ["Atypical Metaplasia", "Atypical metaplasia", "Atypical metaplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypical metaplasia", "shortest_name_length": 19}
{"curie": "MONDO:0018117", "names": ["disorder of phospholipids, sphingolipids and fatty acids biosynthesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of phospholipids, sphingolipids and fatty acids biosynthesis", "shortest_name_length": 69}
{"curie": "UMLS:C5420530", "names": ["Unresectable Cervical Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Cervical Carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0016501", "names": ["HPS with pulmonary fibrosis", "Hermansky-Pudlak syndrome with pulmonary fibrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hermansky-Pudlak syndrome with pulmonary fibrosis", "shortest_name_length": 27}
{"curie": "MONDO:0021500", "names": ["tumor benign spleen", "benign spleen tumor", "Benign spleen tumor", "Benign spleen tumour", "benign spleen tumors", "benign tumor of spleen", "Benign tumor of spleen", "Neoplasm benign;spleen", "spleen benign neoplasm", "Benign tumour of spleen", "benign splenic neoplasm", "Benign Splenic Neoplasm", "Benign Neoplasm of Spleen", "Benign neoplasm of spleen", "benign neoplasm of spleen", "benign neoplasm of the spleen", "Benign Neoplasm of the Spleen", "Benign neoplasm of spleen (disorder)", "benign neoplasm of spleen (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of spleen", "shortest_name_length": 19}
{"curie": "MONDO:0014114", "names": ["CFC4", "cardiofaciocutaneous syndrome 4", "CARDIOFACIOCUTANEOUS SYNDROME 4", "MAP2K2 cardiofaciocutaneous syndrome", "cardiofaciocutaneous syndrome type 4", "cardiofaciocutaneous syndrome caused by mutation in MAP2K2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiofaciocutaneous syndrome 4", "shortest_name_length": 4}
{"curie": "UMLS:C3272464", "names": ["Ampulla of Vater Hepatoid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ampulla of Vater Hepatoid Adenocarcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0008580", "names": ["TOES, SPACE BETWEEN FIRST AND SECOND", "toes, space between first and second"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "toes, space between first and second", "shortest_name_length": 36}
{"curie": "MONDO:0032823", "names": ["MRD60", "INTELLECTUAL DEVELOPMENTAL DISORDER 60 WITH SEIZURES", "intellectual developmental disorder 60 with seizures", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 60, WITH SEIZURES", "Mental Retardation, Autosomal Dominant 60, With Seizures", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 60, WITH SEIZURES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder 60 with seizures", "shortest_name_length": 5}
{"curie": "UMLS:C1275047", "names": ["Radiation-Induced Xerostomia", "Radiation-induced xerostomia", "Xerostomia caused by ionizing radiation", "Xerostomia caused by ionising radiation", "Xerostomia caused by ionizing radiation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radiation-induced xerostomia", "shortest_name_length": 28}
{"curie": "MONDO:0019162", "names": ["PHA2", "PHAII", "Gordon syndrome", "Gordon Syndrome", "chloride shunt syndrome", "Chloride shunt syndrome", "hypertensive hyperkalemia", "Hypertensive hyperkalemia", "Spitzer-Weinstein syndrome", "pseudohypoaldosteronism type 2", "Pseudohypoaldosteronism Type 2", "Pseudohypoaldosteronism type 2", "Type II Pseudohypoaldosteronism", "pseudohypoaldosteronism, type 2", "Pseudohypoaldosteronism Type II", "Pseudohypoaldosteronism, type 2", "Pseudohypoaldosteronism Type 2s", "Type II, Pseudohypoaldosteronism", "Type II Pseudohypoaldosteronisms", "pseudohypoaldosteronism, type II", "Pseudohypoaldosteronism, Type II", "Pseudohypoaldosteronism Type IIs", "Type IIs, Pseudohypoaldosteronism", "Pseudohypoaldosteronisms, Type II", "Familial hyperkalemic hypertension", "familial hyperkalemic hypertension", "Mineralocorticoid resistant hyperkalemia", "mineralocorticoid resistant hyperkalemia", "hyperpotassemia and hypertension familial", "Gordon Hyperkalemia Hypertension Syndrome", "Gordon Hyperkalemia-Hypertension Syndrome", "GORDON HYPERKALEMIA-HYPERTENSION SYNDROME", "Gordon hyperkalemia-hypertension syndrome", "Pseudohypoaldosteronism, type 2 (disorder)", "Gordon hyperkalaemia-hypertension syndrome", "Hyperkalemia-Hypertension Syndrome, Gordon", "Syndrome, Gordon Hyperkalemia-Hypertension", "hyperkalemia-hypertension syndrome, Gordon type", "Hyperkalemia-hypertension syndrome, Gordon type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudohypoaldosteronism type 2", "shortest_name_length": 4}
{"curie": "UMLS:C3267097", "names": ["Narcotic bowel syndrome", "Narcotic Bowel Syndrome", "Narcotic Bowel Syndromes", "Bowel Syndrome, Narcotic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Narcotic Bowel Syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0002207", "names": ["disease paget vulva", "disease pagets vulva", "PAGET DISEASE, VULVA", "vulval Paget disease", "Vulvar Paget Disease", "paget's disease vulva", "Vulva Paget's Disease", "vulva Paget's disease", "Vulvar Paget's Disease", "vulvar Paget's disease", "vulval Paget's disease", "Vulvar Paget's disease", "Paget disease of vulva", "Pagets disease of vulva", "Paget's Disease of Vulva", "Paget's disease of vulva", "paget's disease of vulva", "Paget disease of the vulva", "Paget Disease of the Vulva", "Paget disease vulvar cancer", "paget's disease of the vulva", "Paget's disease of the vulva", "Paget's Disease of the Vulva", "mammalian vulva Paget disease", "vulva, Paget's disease of the", "Paget's disease of vulva (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulval Paget disease", "shortest_name_length": 19}
{"curie": "UMLS:C3897938", "names": ["Persistent Oligoarticular JIA", "Persistent Oligoarticular Juvenile Idiopathic Arthritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Persistent Oligoarticular Juvenile Idiopathic Arthritis", "shortest_name_length": 29}
{"curie": "UMLS:C0153227", "names": ["Gonococcal endocarditis", "Endocarditis gonococcal", "gonococcal endocarditis", "Endocarditis - gonococcal", "Gonococcal endocarditis (disorder)", "gonococcal endocarditis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gonococcal endocarditis", "shortest_name_length": 23}
{"curie": "MONDO:0034671", "names": ["non-syndromic complex polydactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-syndromic complex polydactyly", "shortest_name_length": 33}
{"curie": "MONDO:0006895", "names": ["tumor penis", "penis tumor", "Penis tumor", "Penile tumor", "penile tumor", "penis tumour", "penis tumors", "Penile Tumor", "Penis tumour", "Tumor of Penis", "Penis Neoplasm", "penis neoplasm", "Tumor of penis", "tumor of penis", "penile neoplasm", "Neoplasm, Penis", "Penile Neoplasm", "Penile neoplasm", "Penis Neoplasms", "Tumour of penis", "Penile neoplasms", "Penile Neoplasms", "Neoplasms, Penis", "Neoplasm, Penile", "penile neoplasms", "Neoplasm of Penis", "neoplasm of penis", "Neoplasm of penis", "Neoplasms, Penile", "Tumor of the Penis", "tumor of the penis", "Penile neoplasm NOS", "Neoplasm of the Penis", "Neoplasm of the penis", "neoplasm of the penis", "penile benign neoplasm", "Neoplasia of the penis", "penis neoplasm (disease)", "Neoplasm of penis (disorder)", "neoplasm of penis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "penile neoplasm", "shortest_name_length": 11}
{"curie": "MONDO:0011982", "names": ["AITD3", "AUTOIMMUNE THYROID DISEASE, SUSCEPTIBILITY TO, 3", "autoimmune thyroid disease, susceptibility to, 3", "autoimmune thyroid disease, susceptibility to, type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune thyroid disease, susceptibility to, 3", "shortest_name_length": 5}
{"curie": "UMLS:C1862061", "names": ["Iris pigment epithelial cyst", "Pigmented Epithelial Cyst of the Iris"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Iris pigment epithelial cyst", "shortest_name_length": 28}
{"curie": "UMLS:C4520898", "names": ["Stage IV Breast Cancer", "stage IV breast cancer", "Breast Cancer Stage IV", "Stage IV Breast Carcinoma", "Breast Carcinoma Stage IV", "Stage IV Breast Cancer AJCC v7", "Stage IV Breast Cancer AJCC v6", "Stage IV Breast Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Breast Cancer AJCC v6 and v7", "shortest_name_length": 22}
{"curie": "MONDO:0005544", "names": ["hippocampal sclerosis of aging"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hippocampal sclerosis of aging", "shortest_name_length": 30}
{"curie": "MONDO:0013523", "names": ["NGPS", "PSCOO", "NESTOR-GUILLERMO PROGERIA SYNDROME", "Nestor Guillermo progeria syndrome", "Nestor-Guillermo progeria syndrome", "NGPS - Nestor Guillermo progeria syndrome", "Nestor Guillermo progeria syndrome (disorder)", "Nestor Guillermo progeria syndrome (diagnosis)", "Progeria syndrome, childhood-onset, with osteolysis", "progeria syndrome, childhood-onset, with osteolysis", "PROGERIA SYNDROME, CHILDHOOD-ONSET, WITH OSTEOLYSIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nestor-Guillermo progeria syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C4016019", "names": ["DNA Ligase I Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DNA Ligase I Deficiency", "shortest_name_length": 23}
{"curie": "MONDO:0024969", "names": ["Animal Parasitic Disease", "animal parasitic disease", "Animal Parasitic Diseases", "disease, animal parasitic", "Parasitic Disease, Animal", "Disease, Animal Parasitic", "animal parasitic diseases", "parasitic disease, animal", "Animal Parasitic Infection", "Parasitic Diseases, Animal", "Diseases, Animal Parasitic", "diseases, animal parasitic", "Animal Parasitic Infections", "Infection, Animal Parasitic", "Parasitic Infection, Animal", "Parasitic Infections, Animal", "Infections, Animal Parasitic", "parasitic disease, non-human animal", "parasitic infectious disease, non-human animal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parasitic disease, non-human animal", "shortest_name_length": 24}
{"curie": "MONDO:0015302", "names": ["NLCA", "PLCNA", "Nodular amyloidosis", "Cutaneous nodular amyloidosis", "cutaneous nodular amyloidosis", "nodular cutaneous amyloidosis", "Nodular cutaneous amyloidosis", "amyloidosis cutis nodularis atrophicans", "amyloidosis nodular localized cutaneous", "Primary localized cutaneous nodular amyloidosis", "primary localized cutaneous nodular amyloidosis", "Primary localised cutaneous nodular amyloidosis", "PLCNA - Primary localized cutaneous nodular amyloidosis", "PLCNA - Primary localised cutaneous nodular amyloidosis", "Primary localized cutaneous nodular amyloidosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nodular cutaneous amyloidosis", "shortest_name_length": 4}
{"curie": "UMLS:C1332980", "names": ["Childhood Peripheral T Cell Lymphoma", "Pediatric Peripheral T Cell Lymphoma", "Childhood Mature T- and NK-Cell Lymphoma", "Childhood Mature T-Cell and NK-Cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Mature T-Cell and NK-Cell Non-Hodgkin Lymphoma", "shortest_name_length": 36}
{"curie": "MONDO:0043004", "names": ["Weil", "disease weil", "Weil Disease", "weil disease", "WEIL DISEASE", "Weil disease", "Weils Disease", "Disease, Weil", "disease, Weil", "Weils disease", "weils disease", "Weil's disease", "Weil's Disease", "weil's disease", "Disease, Weil's", "disease, Weil's", "FIEDLER DISEASE", "Weil's syndrome", "spirochetal jaundice", "Spirochetal jaundice", "Spirochetal Jaundice", "spirochaetal jaundice", "spirochetal; jaundice", "Icteric leptospirosis", "jaundice, spirochetal", "jaundice; spirochetal", "Spirochaetal jaundice", "Jaundice, Spirochetal", "JAUNDICE, SPIROCHETAL", "icteric leptospirosis", "jaundice; leptospiral", "leptospiral; jaundice", "Weil's syndrome (diagnosis)", "spirochetal; epidemic jaundice", "leptospiral; epidemic jaundice", "epidemic; jaundice, leptospiral", "Icterohemorrhagic leptospirosis", "Icterohemorrhagic Leptospirosis", "jaundice; epidemic, leptospiral", "LEPTOSPIROSIS, ICTEROHEMORRHAGIC", "Hemorrhagic leptospiral jaundice", "leptospirosis, icterohemorrhagic", "leptospirosis icterohemorrhagica", "Icteric leptospirosis (disorder)", "Leptospirosis, Icterohemorrhagic", "Leptospirosis icterohemorrhagica", "Haemorrhagic leptospiral jaundice", "icterohemorrhagica; leptospirosis", "Leptospirosis icterohaemorrhagica", "Spirochaetosis icterohemorrhagica", "leptospirosis; icterohemorrhagica", "Hemorrhagic spirochaetal jaundice", "Haemorrhagic spirochaetal jaundice", "Leptospiral or spirochetal jaundice", "LANCEREAUX-MATHIEU-WEIL SPIROCHETOSIS", "Hemorrhagic leptospirosis with jaundice", "Infection due to Leptospira interrogans", "Haemorrhagic leptospirosis with jaundice", "leptospirosis icterohemorrhagica (diagnosis)", "Infection due to Leptospira icterohemorrhagiae", "Hemorrhagic leptospiral or spirochetal jaundice", "Leptospiral or spirochetal jaundice (hemorrhagic)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Weil's disease", "shortest_name_length": 4}
{"curie": "UMLS:C4526592", "names": ["Stage IVA Thymus Epithelial Neoplasm", "Stage IVA Thymus Epithelial Neoplasm AJCC v8", "Stage IVA Thymic Epithelial Neoplasm AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Thymic Epithelial Neoplasm AJCC v8", "shortest_name_length": 36}
{"curie": "MONDO:0011885", "names": ["TINU", "ATIN", "Acute T.I.N.", "TINU syndrome", "Dobrin syndrome", "Acute T.I.N., NOS", "Acute interstitial nephritis", "Interstitial nephritis acute", "acute interstitial nephritis", "Nephritis interstitial acute", "NEPHRITIS INTERSTITIAL ACUTE", "INTERSTITIAL NEPHRITIS ACUTE", "NEPHRITIS, ACUTE INTERSTITIAL", "Acute tubulointerstitial disease", "Acute interstitial nephritis, NOS", "acute Tubulointerstitial nephritis", "AIN - Acute interstitial nephritis", "Acute Tubulointerstitial Nephritis", "Acute tubulointerstitial nephritis", "ACUTE TUBULOINTERSTITIAL NEPHRITIS", "acute nephritis tubulo-interstitial", "Acute tubulo-interstitial nephritis", "acute tubulo-interstitial nephritis", "Acute tubulointerstitial disease, NOS", "acute interstitial nephritis (diagnosis)", "Tubulointerstitial nephritis and uveitis", "Tubulointerstitial Nephritis and Uveitis", "TUBULOINTERSTITIAL nephritis with uveitis", "Tubulointerstitial Nephritis with Uveitis", "TUBULOINTERSTITIAL NEPHRITIS WITH UVEITIS", "ATIN - Acute tubulo-interstitial nephritis", "Acute tubulointerstitial nephritis (disorder)", "acute tubulo-interstitial nephritis (diagnosis)", "tubulointerstitial nephritis and uveitis syndrome", "Tubulointerstitial nephritis and uveitis syndrome", "Tubulointerstitial nephritis with uveitis syndrome", "tubulo-interstitial nephritis with uveitis syndrome", "Acute tubulointerstitial nephritis and uveitis syndrome", "acute tubulointerstitial nephritis and uveitis syndrome", "TINU - Tubulointerstitial nephritis with uveitis syndrome", "Tubulointerstitial nephritis with uveitis syndrome (disorder)", "tubulo-interstitial nephritis with uveitis syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tubulointerstitial nephritis and uveitis syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0206504", "names": ["EARDRUM RUPTURE", "rupture eardrum", "eardrum rupture", "eardrum ruptures", "rupture; ear drum", "ear drum ruptured", "RUPTURED EAR DRUM", "ruptured ear drum", "ear drum; rupture", "drum ear ruptured", "perforated eardrum", "eardrum perforated", "drums ear ruptured", "Perforated eardrum", "Rupture of ear drum", "drums ear rupturing", "eardrums perforated", "eardrum perforation", "Eardrum Perforation", "drum ear perforation", "Perforation ear drum", "Perforation, Eardrum", "Perforation;ear drum", "Ear drum perforation", "EAR DRUM PERFORATION", "ear drum perforation", "perforation ear drum", "tympanum; perforation", "perforation; tympanum", "Perforation of eardrum", "perforation of eardrum", "Perforation of ear drum", "perforation of ear drum", "Tympanic Membrane Rupture", "Tear of tympanic membrane", "tympanic membrane rupture", "membrana tympani; rupture", "membrane rupture tympanic", "Membrane Rupture, Tympanic", "tympanic membrane; rupture", "rupture; tympanic membrane", "Rupture, Tympanic Membrane", "Perforation of ear drum NOS", "Rupture of tympanic membrane", "PERFORATED TYMPANIC MEMBRANE", "Perforation;tympanic membran", "perforated tympanic membrane", "Perforation of ear drum, NOS", "perforation of the ear Drums", "TYMPANIC MEMBRANE PERFORATION", "tympanic membrane perforation", "Tympanic Membrane Perforation", "Tympanic membrane perforation", "Perforation tympanic membrane", "Membrane Perforation, Tympanic", "TYMPANIC MEMBRANE, PERFORATION", "PERFORATION OF TYMPANIC MEMBRANE", "Perforation of tympanic membrane", "Tear of tympanic membrane (disorder)", "perforation of the tympanic membrane", "tympanic membrane perforated (___ mm)", "Perforation of tympanic membrane, NOS", "tympanic membrane perforation (diagnosis)", "Perforation of tympanic membrane (disorder)", "Unspecified perforation of tympanic membrane", "Perforation of tympanic membrane, unspecified", "perforated tympanic membrane (physical finding)", "Unspecified perforation of tympanic membrane, unspecified ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tympanic Membrane Perforation", "shortest_name_length": 15}
{"curie": "UMLS:C0855042", "names": ["Metastatic Extraosseous Ewing Sarcoma", "Metastatic Extraskeletal Ewing Sarcoma", "Metastatic Extraosseous Ewing's Sarcoma", "Metastatic Extra-Osseous Ewing's Sarcoma", "Metastatic Extraskeletal Ewing's Sarcoma", "Extra-osseous Ewing's sarcoma metastatic", "Extra-Osseous Ewing's Sarcoma, Metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extra-osseous Ewing's sarcoma metastatic", "shortest_name_length": 37}
{"curie": "UMLS:C2960319", "names": ["BPOP", "Nora Lesion", "Nora lesion", "Nora's Lesion", "bizarre parosteal osteochondromatous proliferation", "Bizarre parosteal osteochondromatous proliferation", "Bizarre Parosteal Osteochondromatous Proliferation", "Bizarre parosteal osteochondromatous proliferation (disorder)", "bizarre parosteal osteochondromatous proliferation (diagnosis)", "Bizarre parosteal osteochondromatous proliferation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bizarre parosteal osteochondromatous proliferation", "shortest_name_length": 4}
{"curie": "MONDO:0004096", "names": ["Spinal Cord Dermoid", "spinal cord dermoid", "Spinal Cord Dermoid Cyst", "spinal cord dermoid cyst", "dermoid cyst of spinal cord", "Dermoid cyst of spinal cord", "Dermoid Cyst of Spinal Cord", "Dermoid Cyst of the Spinal Cord", "dermoid cyst of the spinal cord", "Dermoid cyst of spinal cord (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal cord dermoid cyst", "shortest_name_length": 19}
{"curie": "MONDO:0011599", "names": ["BSCR", "Bscr", "Birdshot lesions", "Birdshot laesions", "chorioretinitis birdshot", "vitiliginous choroiditis", "Birdshot Chorioretinitis", "birdshot chorioretinitis", "Vitiliginous choroiditis", "Birdshot chorioretinitis", "Chorioretinitis, Birdshot", "birdshot chorioretinopathy", "Birdshot chorioretinopathy", "Birdshot retinochoroiditis", "Birdshot Retinochoroiditis", "BIRDSHOT CHORIORETINOPATHY", "Birdshot Chorioretinopathy", "birdshot retinochoroiditis", "Birdshot choroidal lesions", "Chorioretinopathy, Birdshot", "Retinochoroiditis, Birdshot", "Vitiliginous chorioretinitis", "Birdshot Chorioretinopathies", "Birdshot Retinochoroiditides", "Birdshot retinochoroidopathy", "birdshot retinochoroidopathy", "Birdshot Retinochoroidopathy", "Retinochoroidopathy, Birdshot", "Birdshot Retinochoroidopathies", "Birdshot chorioretinitis (disorder)", "Birdshot chorioretinitis (diagnosis)", "[OBSOLETE] Birdshot chorioretinopathy", "multiple small, cream-colored lesions, symmetrically scattered mainly around the optic disk"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "birdshot chorioretinopathy", "shortest_name_length": 4}
{"curie": "MONDO:0007460", "names": ["SENSORY DISCRIMINATION", "sensory discrimination", "discrimination, TWO-point, reduction IN", "discrimination, Two-point, reduction 1N", "DISCRIMINATION, TWO-POINT, REDUCTION IN", "discrimination, Two-point, reduction type 1N"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "discrimination, Two-point, reduction 1N", "shortest_name_length": 22}
{"curie": "MONDO:0003481", "names": ["Dysgerminoma", "dysgerminoma", "ovarian dysgerminoma", "Ovarian dysgerminoma", "Ovarian Dysgerminoma", "dysgerminoma of ovary", "Dysgerminoma of Ovary", "Dysgerminoma of ovary", "dysgerminoma, ovarian", "DYSGERMINOMA, MALIGNANT", "Dysgerminoma of the Ovary", "dysgerminoma of the ovary", "ovary dysgerminoma (disease)", "Malignant ovarian dysgerminoma", "Ovarian Germ Cell Dysgerminoma", "ovarian germ cell dysgerminoma", "Germ Cell Dysgerminoma of Ovary", "germ cell dysgerminoma of ovary", "Malignant dysgerminoma of ovary", "dysgerminoma of ovary (diagnosis)", "Germ Cell Dysgerminoma of the Ovary", "germ cell dysgerminoma of the ovary", "Malignant dysgerminoma of ovary (disorder)", "Dysgerminomatous germ cell cancer of the ovary", "Malignant dysgerminomatous germ cell tumor of ovary", "Malignant dysgerminomatous germ cell tumour of ovary", "Malignant dysgerminomatous germ cell tumor of the ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dysgerminoma of ovary", "shortest_name_length": 12}
{"curie": "UMLS:C5555542", "names": ["Recurrent Malignant Choroid Plexus Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Malignant Choroid Plexus Neoplasm", "shortest_name_length": 43}
{"curie": "MONDO:0044101", "names": ["Cornual pregnancy", "cornual pregnancy", "Cornual Pregnancy", "pregnancy, cornual", "Pregnancy, cornual", "cornual; gestation", "cornual; pregnancy", "Pregnancy, Cornual", "pregnancy; cornual", "cornual Pregnancies", "Cornual Pregnancies", "Pregnancies, cornual", "Pregnancies, Cornual", "rudimentary horn pregnancy", "Rudimentary horn pregnancy", "Cornual pregnancy (disorder)", "cornual pregnancy (diagnosis)", "uterine horn ectopic pregnancy", "ectopic pregnancy of uterine horn"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pregnancy, cornual", "shortest_name_length": 17}
{"curie": "MONDO:0015703", "names": ["T-B+ SCID due to CD3delta/CD3epsilon/CD3zeta", "T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta", "shortest_name_length": 44}
{"curie": "MONDO:0034823", "names": ["OFD18", "orofaciodigital syndrome type 18", "oral-facial-digital syndrome type 18", "oral-facial-digital syndrome with short stature and brachymesophalangy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oral-facial-digital syndrome with short stature and brachymesophalangy", "shortest_name_length": 5}
{"curie": "MONDO:0005531", "names": ["morphinism", "addiction morphine", "morphine addiction", "Morphine Addiction", "Addiction, Morphine", "morphine dependence", "Morphine dependence", "addictions morphine", "Morphine Dependence", "Dependence, Morphine", "morphine; dependence", "dependence; morphine", "opioid dependence morphine", "Morphine dependence (disorder)", "Morphine dependence (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "morphine dependence", "shortest_name_length": 10}
{"curie": "UMLS:C0392175", "names": ["Renal bleeding", "Renal Hemorrhage", "Renal hemorrhage", "kidney hemorrhage", "Renal haemorrhage", "Hemorrhage kidney", "HEMORRHAGE KIDNEY", "kidney; hemorrhage", "hemorrhage; kidney", "Haemorrhage kidney", "Hemorrhage of kidney", "Haemorrhage of kidney", "Hemorrhage of kidney (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemorrhage of kidney", "shortest_name_length": 14}
{"curie": "MONDO:0009352", "names": ["CBS deficiency", "CBS DEFICIENCY", "CBS Deficiency", "Deficiency, CBS", "CBS Deficiencies", "Deficiencies, CBS", "Classic homocystinuria", "classic homocystinuria", "Deficiency of beta-thionase", "thrombosis, hyperhomocysteinemic", "Deficiency of serine sulfhydrase", "Deficiency of serine sulphydrase", "homocystinuria due to CBS deficiency", "Deficiency of methylcysteine synthase", "cystathionine beta-synthase deficiency", "CYSTATHIONINE BETA-SYNTHASE DEFICIENCY", "Cystathionine beta-synthase deficiency", "Cystathionine Beta Synthase Deficiency", "HYPERHOMOCYSTEINEMIA, THROMBOTIC, CBS-RELATED", "hyperhomocysteinemia, thrombotic, CBS-related", "Cystathionine beta-Synthase Deficiency Disease", "Cystathionine beta Synthase Deficiency Disease", "Deficiency Disease, Cystathionine beta-Synthase", "Deficiency Disease, Cystathionine beta Synthase", "Cystathionine beta-synthase deficiency (disorder)", "homocystinuria with or without response to pyridoxine", "HOMOCYSTINURIA WITH OR WITHOUT RESPONSE TO PYRIDOXINE", "homocystinuria, B6-responsive and nonresponsive types", "HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY", "Homocystinuria due to cystathionine beta-synthase deficiency", "homocystinuria due to cystathionine beta-synthase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "classic homocystinuria", "shortest_name_length": 14}
{"curie": "MONDO:0017790", "names": ["GAPPS", "gastric polyp", "polyp stomach", "Gastric polyp", "polyp gastric", "Gastric Polyp", "stomach polyp", "GASTRIC POLYP", "Gastric polyps", "polyp; stomach", "stomach polyps", "gastric polyps", "stomach; polyp", "polyps gastric", "polyps stomach", "GASTRIC POLYPS", "Gastric Polyposa", "Polyp(s);stomach", "Polyp of stomach", "Gastric polyposis", "Polyps of Stomach", "Polyposis gastric", "POLYPOSIS GASTRIC", "gastric polyposis", "Gastric Polyposis", "Gastritis polyposa", "polyposis, gastric", "Gastric polyp, NOS", "Polyposis, Gastric", "Polyps of the Stomach", "fundic gland polyposis", "Multiple gastric polyps", "Gastric polyp (disorder)", "gastric polyps (diagnosis)", "Gastric polyposis (disorder)", "gastric polyposis (diagnosis)", "familial fundic gland polyposis with gastric cancer", "Familial fundic gland polyposis with gastric cancer", "polyposis, gastric, Dos Santos and de Magalhaes 1980", "Gastric adenocarcinoma and proximal polyposis of stomach", "Gastric Adenocarcinoma and Proximal Polyposis of the Stomach", "gastric adenocarcinoma and proximal polyposis of the stomach", "GAPPS - gastric adenocarcinoma and proximal polyposis of stomach", "Gastric adenocarcinoma and proximal polyposis of stomach (disorder)", "Gastric adenocarcinoma and proximal polyposis of stomach (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric adenocarcinoma and proximal polyposis of the stomach", "shortest_name_length": 5}
{"curie": "UMLS:C1336188", "names": ["Stage IIB Nasopharynx Carcinoma", "Stage IIB Carcinoma of Nasopharynx", "Stage IIB Nasopharyngeal Carcinoma", "Stage IIB Carcinoma of the Nasopharynx"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Nasopharyngeal Carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0009706", "names": ["HML", "ISCU myopathy", "aconitase deficiency", "Aconitase deficiency", "Myopathy with Deficiency of ISCU", "iron-sulfur cluster deficiency myopathy", "Iron-Sulfur Cluster Deficiency Myopathy", "Iron-sulfur cluster deficiency myopathy", "Myoglobinuria due to Abnormal Glycolysis", "Hereditary Myopathy with Lactic Acidosis", "myoglobinuria due to abnormal glycolysis", "MYOGLOBINURIA DUE TO ABNORMAL GLYCOLYSIS", "Hereditary myopathy with lactic acidosis", "Myoglobinuria due to abnormal glycolysis", "MYOPATHY WITH LACTIC ACIDOSIS, HEREDITARY", "Myopathy with Lactic Acidosis, Hereditary", "myopathy with lactic acidosis, hereditary", "Myopathy with exercise intolerance, Swedish type", "myopathy with exercise intolerance, Swedish type", "Myopathy with Exercise Intolerance, Swedish Type", "MYOPATHY WITH EXERCISE INTOLERANCE, SWEDISH TYPE", "hereditary myopathy with lactic acidosis due to ISCU deficiency", "Myopathy with deficiency of iron-sulfur cluster assembly enzyme", "Myopathy with Deficiency of Iron-Sulfur Cluster Assembly Enzyme", "Hereditary myopathy with lactic acidosis due to ISCU deficiency", "Myopathy with deficiency of iron-sulphur cluster assembly enzyme", "Myopathy with deficiency of succinate dehydrogenase and aconitase", "MYOPATHY WITH DEFICIENCY OF SUCCINATE DEHYDROGENASE AND ACONITASE", "myopathy with deficiency of succinate dehydrogenase and aconitase", "Myopathy with Deficiency of Succinate Dehydrogenase and Aconitase", "Myopathy with deficiency of iron-sulfur cluster assembly enzyme (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary myopathy with lactic acidosis due to ISCU deficiency", "shortest_name_length": 3}
{"curie": "MONDO:0032755", "names": ["NEDBA", "NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT VARIABLE BRAIN ABNORMALITIES", "neurodevelopmental disorder with or without variable brain abnormalities; NEDBA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with or without variable brain abnormalities; NEDBA", "shortest_name_length": 5}
{"curie": "MONDO:0005446", "names": ["Delhi", "Delhi boil", "DELHI BOIL", "Natal sore", "sore; Natal", "Aleppo boil", "BAGDAD BOIL", "Delhi; boil", "sore; Delhi", "boil; Delhi", "Delhi; sore", "Natal; sore", "Baghdad boil", "Aleppo; boil", "boil; Aleppo", "Oriental Sore", "oriental sore", "Baghdad; boil", "ALEPPO BUTTON", "biskra button", "Oriental sore", "boil; Baghdad", "Biskra button", "ORIENTAL SORE", "oriental; sore", "sore; oriental", "Sore, Oriental", "Biskra's button", "leishmaniasis; skin", "skin; leishmaniasis", "Leproid leishmaniasis", "leproid leishmaniasis", "Oriental leishmaniasis", "cutaneous leishmaniasis", "DELHI BOIL, ALEPPO BOIL", "Cutaneous Leishmaniasis", "leishmaniasis cutaneous", "cutaneous Leishmaniasis", "Old World Leishmaniasis", "Cutaneous Leishmaniases", "Cutaneous leishmaniasis", "Leishmaniasis, Old World", "leishmaniasis; Old World", "cutaneous; leishmaniasis", "leishmaniasis; cutaneous", "Old World; leishmaniasis", "Leishmaniases, Cutaneous", "Leishmaniasis, cutaneous", "Leishmaniasis, Cutaneous", "zone of skin leishmaniasis", "Urban cutaneous leishmaniasis", "Cutaneous urban leishmaniasis", "Cutaneous, urban leishmaniasis", "Cutaneous leishmaniasis, urban", "diffuse cutaneous leishmaniasis", "Leishmaniasis, cutaneous, urban", "Old World cutaneous leishmaniasis", "old world cutaneous leishmaniasis", "Cutaneous leishmaniasis, dry form", "LEISHMANIASIS, OLD WORLD CUTANEOUS", "Cutaneous leishmaniasis (disorder)", "Dry form of cutaneous leishmaniasis", "Cutaneous leishmaniasis (diagnosis)", "Asian Desert Cutaneous Leishmaniasis", "Asian desert cutaneous leishmaniasis", "Cutaneous, asian desert leishmaniasis", "Infection by Leishmania tropica major", "Cutaneous leishmaniasis, Asian desert", "Anthroponotic cutaneous leishmaniasis", "Leishmaniasis, cutaneous, Asian desert", "dry form old world cutaneous leishmaniasis", "ACL - Anthroponotic cutaneous leishmaniasis", "old world cutaneous leishmaniasis (diagnosis)", "Dry form of cutaneous leishmaniasis (disorder)", "Asian desert cutaneous leishmaniasis (disorder)", "Asian desert cutaneous leishmaniasis (diagnosis)", "dry form old world cutaneous leishmaniasis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous leishmaniasis", "shortest_name_length": 5}
{"curie": "MONDO:0000459", "names": ["mesenchymal glioblastoma", "Mesenchymal Glioblastoma", "glioblastoma mesenchymal subtype"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mesenchymal glioblastoma", "shortest_name_length": 24}
{"curie": "UMLS:C1709572", "names": ["Pleural Desmoplastic Mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pleural Desmoplastic Mesothelioma", "shortest_name_length": 33}
{"curie": "MONDO:0043237", "names": ["Glossalgia", "glossalgia", "sore tongue", "TONGUE SORE", "Tongue sore", "TONGUE PAIN", "Glossodynia", "Glossalgias", "tongue pain", "Tongue Pain", "Pain;tongue", "PAIN TONGUE", "Sore tongue", "Pain tongue", "Tongue pain", "tongue sore", "glossodynia", "Glossodynias", "pain; tongue", "tongue; pain", "Glossopyroses", "glossopyrosis", "painful tongue", "Tongue painful", "Painful Tongue", "Pain of tongue", "Painful tongue", "tongue soreness", "soreness of tongue", "Soreness of tongue", "Glossodynia (disorder)", "glossodynia (diagnosis)", "Pain of tongue (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glossodynia", "shortest_name_length": 10}
{"curie": "MONDO:0019787", "names": ["Autoimmune enteropathy", "Autoimmune Enteropathy", "autoimmune enteropathy", "Enteropathy, autoimmune", "Autoimmune enteropathy (disorder)", "severe immune-mediated enteropathy", "Severe immune-mediated enteropathy", "Autoimmune enteropathy (diagnosis)", "malabsorption syndrome autoimmune enteropathy", "immune-mediated protracted diarrhea of infancy", "Immune-mediated protracted diarrhea of infancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune enteropathy", "shortest_name_length": 22}
{"curie": "UMLS:C1332231", "names": ["Aleukemic Lymphoblastic Leukemia Cutis", "Aleukemic Acute Lymphoblastic Leukemia Cutis", "Aleukemic Precursor Lymphoblastic Leukemia Cutis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aleukemic Acute Lymphoblastic Leukemia Cutis", "shortest_name_length": 38}
{"curie": "UMLS:C1336815", "names": ["Transplant-Related Renal Cell Cancer", "Transplant-Related Renal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transplant-Related Renal Cell Carcinoma", "shortest_name_length": 36}
{"curie": "UMLS:C1336407", "names": ["Stage IVC Oropharynx Epidermoid Carcinoma", "Stage IVC Oropharynx Squamous Cell Carcinoma", "Stage IVC Epidermoid Carcinoma of Oropharynx", "Stage IVC Oropharyngeal Epidermoid Carcinoma", "Stage IVC Oropharyngeal Squamous Cell Carcinoma", "Stage IVC Squamous Cell Carcinoma of Oropharynx", "Stage IVC Epidermoid Carcinoma of the Oropharynx", "Stage IVC Squamous Cell Carcinoma of the Oropharynx", "Stage IVC Oropharyngeal Throat Squamous Cell Cancer", "Stage IVC Oropharyngeal Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Oropharyngeal Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 41}
{"curie": "MONDO:0001372", "names": ["bladder neck cancer", "BLADDER NECK CANCER", "neck of urinary bladder cancer", "malignant tumor of bladder neck", "Malignant tumor of bladder neck", "Malignant tumour of bladder neck", "cancer of neck of urinary bladder", "Malignant neoplasm of bladder neck", "malignant tumor of neck of bladder", "malignant neoplasm of neck of bladder", "Malignant neoplasm of urinary bladder neck", "malignant neck of urinary bladder neoplasm", "malignant neoplasm of urinary bladder neck", "Malignant tumor of bladder neck (disorder)", "malignant neoplasm of neck of urinary bladder", "malignant neoplasm of neck of bladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder neck cancer", "shortest_name_length": 19}
{"curie": "MONDO:0100017", "names": ["PRP", "Devergie", "devergie's disease", "Devergie's disease", "Lichen ruber acuminatus", "Pityriasis rubra pilaris", "pityriasis rubra pilaris", "Pityriasis Rubra Pilaris", "PITYRIASIS RUBRA PILARIS", "pityriasis pilaris rubra", "rubra pilaris; pityriasis", "pityriasis; rubra pilaris", "PRP - Pityriasis rubra pilaris", "Pityriasis rubra pilaris (disorder)", "pityriasis rubra pilaris (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pityriasis rubra pilaris", "shortest_name_length": 3}
{"curie": "MONDO:0011608", "names": ["ATOD5", "atopic dermatitis 5", "dermatitis, ATOPIC, 5", "Dermatitis, Atopic, 5", "DERMATITIS, ATOPIC, 5", "dermatitis, atopic, 5", "atopic dermatitis type 5", "dermatitis, atopic, susceptibility to, 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermatitis, atopic, 5", "shortest_name_length": 5}
{"curie": "MONDO:0030507", "names": ["SPGF61", "spermatogenic failure 61", "SPERMATOGENIC FAILURE 61"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 61", "shortest_name_length": 6}
{"curie": "UMLS:C5555032", "names": ["Mucosal Melanoma of the Female Genital Tract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mucosal Melanoma of the Female Genital Tract", "shortest_name_length": 44}
{"curie": "MONDO:0002460", "names": ["lacrimal system tumor", "Lacrimal System Tumor", "lacrimal system cancer", "tumor of lacrimal system", "Tumor of Lacrimal System", "Tumor of lacrimal system", "lacrimal system neoplasm", "Lacrimal System Neoplasm", "lacrimal system neoplasms", "Tumour of lacrimal system", "lacrimal apparatus cancer", "Lacrimal System Neoplasms", "Neoplasm of Lacrimal System", "Neoplasm of lacrimal system", "neoplasm of lacrimal system", "Tumor of lacrimal apparatus", "Lacrimal Apparatus Neoplasm", "Tumour of lacrimal apparatus", "eye neoplasm lacrimal system", "Tumor of the Lacrimal System", "cancer of lacrimal apparatus", "tumor of the lacrimal system", "Neoplasm of lacrimal apparatus", "Neoplasm of the Lacrimal System", "neoplasm of the lacrimal system", "malignant lacrimal apparatus neoplasm", "Neoplasm of lacrimal system (disorder)", "Neoplasm of lacrimal system (diagnosis)", "malignant neoplasm of lacrimal apparatus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lacrimal system cancer", "shortest_name_length": 21}
{"curie": "UMLS:C0235957", "names": ["myonecrosis", "Myonecrosis", "muscle necrosis", "Muscle necrosis", "MUSCLE NECROSIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Muscle necrosis", "shortest_name_length": 11}
{"curie": "MONDO:0024888", "names": ["Mesonephroma", "mesonephroma", "mesonephric tumor", "Mesonephric Tumor", "Wolffian duct tumor", "Wolffian Duct Tumor", "mesonephric neoplasm", "Mesonephric Neoplasm", "Wolffian duct neoplasm", "Wolffian Duct Neoplasm", "mesonephric duct tumor", "mesonephric duct neoplasm", "tumor of mesonephric duct", "neoplasm of mesonephric duct"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mesonephric neoplasm", "shortest_name_length": 12}
{"curie": "UMLS:C1527352", "names": ["Wilson Disease, Hepatic Form", "Hepatic Form of Wilson Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatic Form of Wilson Disease", "shortest_name_length": 28}
{"curie": "UMLS:C4521621", "names": ["Stage IVA Bone Cancer", "Stage IVA Bone Cancer AJCC v8", "Stage IVA Appendicular Skeleton, Trunk, Skull, and Facial Bones Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Bone Cancer AJCC v8", "shortest_name_length": 21}
{"curie": "MONDO:0012996", "names": ["CCDS3", "AGAT DEFICIENCY", "AGAT deficiency", "AGAT Deficiency", "GATM deficiency", "GATM Deficiency", "GATM DEFICIENCY", "CEREBRAL CREATINE DEFICIENCY SYNDROME 3", "cerebral creatine deficiency syndrome 3", "Cerebral creatine deficiency syndrome 3", "glycine amidinotransferase activity disease", "cerebral creatine deficiency syndrome type 3", "arginine glycine amidinotransferase deficiency", "Arginine:Glycine Amidinotransferase Deficiency", "ARGININE:GLYCINE AMIDINOTRANSFERASE DEFICIENCY", "Arginine:glycine amidinotransferase deficiency", "arginine:glycine amidinotransferase deficiency", "Arginine-Glycine Amidinotransferase Deficiency", "disorder of glycine amidinotransferase activity", "L-arginine-glycine amidinotransferase deficiency", "L-arginine:glycine amidinotransferase deficiency", "L-Arginine:Glycine Aminidotransferase Deficiency", "L-Arginine:glycine amidinotransferase deficiency", "Cerebral creatine deficiency syndrome 3 (disorder)", "creatine deficiency syndrome due to AGAT deficiency", "Creatine Deficiency Syndrome due to AGAT Deficiency", "CREATINE DEFICIENCY SYNDROME DUE TO AGAT DEFICIENCY", "Creatine deficiency syndrome due to arginine:glycine amidinotransferase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AGAT deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0019577", "names": ["Anonychia onychodystrophy", "Anonychia-Onychodystrophy", "Absent nails and dystrophic nails", "anonychia-onychodystrophy syndrome", "Anonychia-onychodystrophy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anonychia-onychodystrophy syndrome", "shortest_name_length": 25}
{"curie": "UMLS:C5420768", "names": ["Conjunctival Compound Nevus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conjunctival Compound Nevus", "shortest_name_length": 27}
{"curie": "MONDO:0015066", "names": ["appendix NET", "Appendix NET", "appendiceal NEN", "Appendiceal NEN", "NEN of appendix", "appendix neuroendocrine tumor", "Appendix Neuroendocrine Tumor", "appendiceal neuroendocrine tumor", "Appendix Neuroendocrine Neoplasm", "Neuroendocrine tumor of appendix", "Neuroendocrine tumour of appendix", "appendiceal neuroendocrine neoplasm", "Neuroendocrine neoplasm of appendix", "Appendiceal neuroendocrine neoplasm", "neuroendocrine neoplasm of appendix", "appendix well differentiated endocrine tumor", "Appendix Well Differentiated Endocrine Tumor", "Neuroendocrine neoplasm of appendix (disorder)", "Appendix Well Differentiated Endocrine Tumor/Carcinoma", "appendix well differentiated endocrine tumor/carcinoma", "well-differentiated neuroendocrine tumor of the appendix", "neuroendocrine tumor of the appendix, well differentiated, low or intermediate grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuroendocrine tumor of the appendix, well differentiated, low or intermediate grade", "shortest_name_length": 12}
{"curie": "MONDO:0001871", "names": ["acute diffuse nephritis", "acute nephritis diffuse", "Acute diffuse nephritis", "diffuse acute glomerulonephritis", "Acute Diffuse Glomerulonephritis", "acute Diffuse Glomerulonephritis", "Acute diffuse glomerulonephritis", "acute diffuse glomerulonephritis", "diffuse glomerulonephritis, acute", "Acute diffuse nephritis (disorder)", "Acute diffuse nephritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute diffuse glomerulonephritis", "shortest_name_length": 23}
{"curie": "UMLS:C4763782", "names": ["Refractory T-Cell/Histiocyte-Rich Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory T-Cell/Histiocyte-Rich Large B-Cell Lymphoma", "shortest_name_length": 55}
{"curie": "UMLS:C1336228", "names": ["Stage IIIB Ovarian Germ Cell Tumor", "Stage IIIB Ovarian Germ Cell Tumor AJCC v6", "Stage IIIB Ovarian Germ Cell Tumor AJCC v7", "Stage IIIB Ovarian Germ Cell Tumor AJCC v6 and v7", "FIGO Stage IIIB Malignant Ovarian Germ Cell Tumor", "FIGO Stage IIIB Malignant Germ Cell Tumor of Ovary", "FIGO Stage IIIB Malignant Ovarian Germ Cell Neoplasm", "FIGO Stage IIIB Malignant Germ Cell Neoplasm of Ovary", "FIGO Stage IIIB Malignant Germ Cell Tumor of the Ovary", "FIGO Stage IIIB Malignant Germ Cell Neoplasm of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Ovarian Germ Cell Tumor AJCC v6 and v7", "shortest_name_length": 34}
{"curie": "UMLS:C0334569", "names": ["Odontogenic Myxoma", "Odontogenic myxoma", "myxoma; odontogenic", "odontogenic; myxoma", "Odontogenic Myxofibroma", "Odontogenic myxofibroma", "myxofibroma; odontogenic", "odontogenic; myxofibroma", "Odontogenic myxoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Odontogenic myxoma", "shortest_name_length": 18}
{"curie": "MONDO:0007869", "names": ["Kyrle disease", "KYRLE DISEASE", "Kyrle's disease", "Hyperkeratosis penetrans", "Kyrle's disease (diagnosis)", "Hyperkeratosis parafollicularis", "Hyperkeratosis follicularis in cutem penetrans", "Hyperkeratosis follicularis et parafollicularis", "Acquired hyperkeratosis follicularis in cutem penetrans", "Hyperkeratosis follicularis in cutem penetrans (disorder)", "Keratosis follicularis et parafollicularis in cutem penetrans", "keratosis follicularis et parafollicularis in cutem penetrans", "follicularis; keratosis, et parafollicularis in cutem penetrans", "keratosis; follicularis, et parafollicularis in cutem penetrans", "hyperkeratosis follicularis et parafollicularis in cutem penetrans", "Hyperkeratosis follicularis et parafollicularis in cutem penetrans", "Keratosis follicularis et parafollicularis in cutem penetrans [Kyrle]", "keratosis follicularis et parafollicularis in cutem penetrans (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kyrle disease", "shortest_name_length": 13}
{"curie": "UMLS:C5669679", "names": ["Liver Plasmacytoma", "Plasmacytoma of Liver", "Primary Liver Plasmacytoma", "Primary Extraosseous Liver Plasmacytoma", "Primary Extramedullary Liver Plasmacytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liver Plasmacytoma", "shortest_name_length": 18}
{"curie": "UMLS:C0497471", "names": ["Thrush;genital;F", "female genital thush", "MONILIASIS GENITAL FEMALE", "Moniliasis genital female", "Genital candidiasis female", "Urogenital candidiasis proven"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Moniliasis genital female", "shortest_name_length": 16}
{"curie": "MONDO:0013741", "names": ["ETL5", "familial temporal lobe epilepsy 5", "epilepsy, familial temporal lobe, 5", "EPILEPSY, FAMILIAL TEMPORAL LOBE, 5", "familial temporal lobe epilepsy type 5", "epilepsy, familial temporal lobe, type 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial temporal lobe epilepsy 5", "shortest_name_length": 4}
{"curie": "MONDO:0021509", "names": ["benign myocardial tumor", "Benign Myocardial Tumor", "myocardium benign neoplasm", "Benign Myocardial Neoplasm", "Benign Tumor of Myocardium", "Benign tumor of myocardium", "benign tumor of myocardium", "benign myocardial neoplasm", "Benign tumour of myocardium", "Benign neoplasm of myocardium", "benign neoplasm of myocardium", "Benign Neoplasm of Myocardium", "Benign Tumor of the Myocardium", "benign tumor of the myocardium", "Benign Neoplasm of the Myocardium", "benign neoplasm of the myocardium", "Benign neoplasm of myocardium (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of myocardium", "shortest_name_length": 23}
{"curie": "UMLS:C1334063", "names": ["Hybrid Odontogenic Fibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hybrid Odontogenic Fibroma", "shortest_name_length": 26}
{"curie": "MONDO:0006825", "names": ["kuru", "Kuru", "kuru; disease", "Kuru (disorder)", "kuru (diagnosis)", "Kuru encephalitis", "Kuru Encephalopathy", "kuru encephalopathy", "Kuru agent infection", "Encephalopathy, Kuru", "disease (or disorder); kuru"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kuru", "shortest_name_length": 4}
{"curie": "UMLS:C1336238", "names": ["Stage IIIC Ovarian Germ Cell Tumor", "Stage IIIC Ovarian Germ Cell Tumor AJCC v6", "Stage IIIC Ovarian Germ Cell Tumor AJCC v7", "Stage IIIC Ovarian Germ Cell Tumor AJCC v6 and v7", "FIGO Stage IIIC Malignant Ovarian Germ Cell Tumor", "FIGO Stage IIIC Malignant Germ Cell Tumor of Ovary", "FIGO Stage IIIC Malignant Ovarian Germ Cell Neoplasm", "FIGO Stage IIIC Malignant Germ Cell Neoplasm of Ovary", "FIGO Stage IIIC Malignant Germ Cell Tumor of the Ovary", "FIGO Stage IIIC Malignant Germ Cell Neoplasm of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Ovarian Germ Cell Tumor AJCC v6 and v7", "shortest_name_length": 34}
{"curie": "UMLS:C5420058", "names": ["Sinonasal Benign Soft Tissue Neoplasm", "Benign Sinonasal Soft Tissue Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Sinonasal Soft Tissue Neoplasm", "shortest_name_length": 37}
{"curie": "MONDO:0012615", "names": ["MRT7", "MRT22", "INTELLECTUAL DEVELOPMENTAL DISORDER 22", "Mental Retardation, Autosomal Recessive 7", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 7", "mental retardation, autosomal recessive 7", "mental retardation, autosomal recessive 22", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 22", "mental retardation, autosomal recessive type 7", "intellectual disability, autosomal recessive 7", "intellectual disability, autosomal recessive 22", "intellectual disability, autosomal recessive type 7", "autosomal recessive intellectual developmental disorder 7", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 7", "TUSC3 autosomal recessive non-syndromic intellectual disability", "autosomal recessive non-syndromic intellectual disability caused by mutation in TUSC3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 7", "shortest_name_length": 4}
{"curie": "MONDO:0018773", "names": ["autosomal dominant distal axonal motor neuropathy-myofibrillar myopathy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant distal axonal motor neuropathy-myofibrillar myopathy syndrome", "shortest_name_length": 80}
{"curie": "MONDO:0010333", "names": ["MRXS28", "Graham-Cox syndrome", "Graham Cox syndrome", "mental retardation, X-linked, syndromic 28", "MENTAL RETARDATION, X-LINKED, SYNDROMIC 28", "intellectual disability, X-linked, syndromic 28", "INTELLECTUAL DEVELOPMENT DISORDER, X-LINKED, SYNDROMIC 28", "corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome", "Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome", "Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome", "agenesis of the corpus callosum-intellectual disability-coloboma-micrognathia syndrome", "corpus callosum, agenesis of, with mental retardation, ocular coloboma and micrognathia", "corpus callosum, agenesis of, with mental retardation, ocular coloboma, and micrognathia", "Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia", "corpus callosum, agenesis of, with intellectual disability, ocular coloboma and micrognathia", "corpus callosum, agenesis of, with intellectual disability, ocular coloboma, and micrognathia", "Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome (disorder)", "Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome (diagnosis)", "CORPUS CALLOSUM, AGENESIS OF, WITH IMPAIRED INTELLECTUAL DEVELOPMENT, OCULAR COLOBOMA, AND MICROGNATHIA", "corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0003896", "names": ["Breast Capillary Angioma", "breast capillary angioma", "Capillary Angioma of Breast", "Capillary Angioma of breast", "breast capillary hemangioma", "capillary angioma of breast", "Breast Capillary Hemangioma", "capillary hemangioma of breast", "Capillary Hemangioma of Breast", "capillary angioma of the breast", "Capillary Angioma of the Breast", "capillary hemangioma of the breast", "Capillary Hemangioma of the Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast capillary hemangioma", "shortest_name_length": 24}
{"curie": "MONDO:0032578", "names": ["CDCBM9", "CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 9", "cortical dysplasia, complex, with other brain malformations 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cortical dysplasia, complex, with other brain malformations 9", "shortest_name_length": 6}
{"curie": "UMLS:C0341498", "names": ["anastomotic leak pancreas", "Pancreatic anastomotic leak", "Pancreatic Anastomotic Leakage", "Pancreatic anastomotic leak (disorder)", "Pancreatic anastomotic leak (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Anastomotic Leakage", "shortest_name_length": 25}
{"curie": "UMLS:C1265998", "names": ["Glassy cell carcinoma", "glassy cell carcinoma", "Glassy Cell Carcinoma", "glassy cell carcinoma (diagnosis)", "Glassy cell carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Glassy cell carcinoma", "shortest_name_length": 21}
{"curie": "MONDO:0008988", "names": ["CTNL1", "CTLN1", "citrullinemia", "Citrullinuria", "ASS deficiency", "Citrullinemia 1", "citrullinemia 1", "Citrullinemia Type I", "Citrullinemia type I", "Type I Citrullinemia", "Citrullinemia type 1", "citrullinemia type 1", "Citrullinemia Type 1", "citrullinemia type I", "Citrullinaemia type I", "Citrullinemia, Type I", "Citrullinemia, type I", "CITRULLINEMIA, TYPE I", "Classic Citrullinemia", "Citrullinaemia type 1", "Classic citrullinemia", "Type I Citrullinemias", "classic citrullinemia", "citrullinemia, type 1", "CITRULLINEMIA, CLASSIC", "Citrullinemia, Classic", "citrullinemia, classic", "Classic citrullinaemia", "Classic Citrullinemias", "Citrullinemias, Classic", "Classical Citrullinemia", "Citrullinemia, Classical", "Classical Citrullinemias", "Citrullinemia type I (disorder)", "Argininosuccinate synthase deficiency", "argininosuccinate synthase deficiency", "Argininosuccinate synthetase deficiency", "Argininosuccinate Synthetase Deficiency", "argininosuccinate synthetase deficiency", "Argininosuccinic acid synthase deficiency", "argininosuccinic acid synthase deficiency", "Argininosuccinic acid synthetase deficiency", "argininosuccinic acid synthetase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "citrullinemia type I", "shortest_name_length": 5}
{"curie": "MONDO:0015006", "names": ["EBS6", "EBSSH", "epidermolysis bullosa simplex, generalized, with scarring and hair loss", "EPIDERMOLYSIS BULLOSA SIMPLEX, GENERALIZED, WITH SCARRING AND HAIR LOSS", "EPIDERMOLYSIS BULLOSA SIMPLEX 6, GENERALIZED, WITH SCARRING AND HAIR LOSS", "epidermolysis bullosa simplex 6, generalized, with scarring and hair loss", "epidermolysis bullosa simplex, generalized, with scarring and hair loss; EBSSH", "generalized basal epidermolysis bullosa simplex with skin atrophy, scarring and hair loss"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolysis bullosa simplex 6, generalized, with scarring and hair loss", "shortest_name_length": 4}
{"curie": "MONDO:0014234", "names": ["RPK", "RAK", "RAPK", "ACROPIGMENTATIO RETICULARIS", "acropigmentatio reticularis", "reticulate pigmentation of Kitamura", "RETICULATE PIGMENTATION OF KITAMURA", "Kitamura reticulate acropigmentation", "KITAMURA RETICULATE ACROPIGMENTATION", "Kitamura Reticulate Acropigmentation", "Kitamura's reticulate acropigmentation", "RETICULATE ACROPIGMENTATION OF KITAMURA", "reticulate acropigmentation of Kitamura", "Reticulate Acropigmentation of Kitamura", "Reticulate acropigmentation of Kitamura", "Reticulate acropigmentation of Kitamura (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "reticulate acropigmentation of Kitamura", "shortest_name_length": 3}
{"curie": "UMLS:C4288003", "names": ["Vulvar Merkel Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Merkel Cell Carcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0017618", "names": ["CSID with starch intolerance", "disaccharide intolerance with starch intolerance", "congenital sucrose intolerance with starch intolerance", "congenital sucrase-isomaltase deficiency with starch intolerance", "congenital sucrase-isomaltose malabsorption with starch intolerance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital sucrase-isomaltase deficiency with starch intolerance", "shortest_name_length": 28}
{"curie": "MONDO:0010577", "names": ["DFN2", "DFNX1", "X-linked deafness 1", "deafness, X-linked 1", "Deafness, X-Linked 1", "DEAFNESS, X-LINKED 1", "hearing loss, X-linked 1", "deafness, X-linked type 1", "X-linked sensorineural congenital deafness 2", "Deafness, X-Linked 2, Sensorineural Congenital", "deafness, X-linked 2, sensorineural congenital", "DEAFNESS, X-LINKED 2, SENSORINEURAL CONGENITAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, X-linked 1", "shortest_name_length": 4}
{"curie": "MONDO:0022887", "names": ["craniofrontonasal syndrome Teebi type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniofrontonasal syndrome Teebi type", "shortest_name_length": 37}
{"curie": "MONDO:0005125", "names": ["Group B leprosy", "Type BB leprosy", "Dimorphic leprosy", "borderline leprosy", "Borderline Leprosy", "Borderline leprosy", "Dimorphous Leprosy", "LEPROSY, BORDERLINE", "leprosy; borderline", "borderline; leprosy", "LEPROSY, DIMORPHOUS", "Leprosy, Dimorphous", "dimorphous; leprosy", "Leprosy, Borderline", "leprosy; dimorphous", "Dimorphous Leprosies", "Borderline Leprosies", "Midborderline leprosy", "Leprosies, Borderline", "Leprosies, Dimorphous", "BB - Borderline leprosy", "borderline leprosy [group B]", "Borderline leprosy [group B]", "Borderline leprosy (group b)", "Borderline leprosy (disorder)", "borderline leprosy (diagnosis)", "Midborderline leprosy (disorder)", "Borderline or dimorphous leprosy", "borderline or dimorphous leprosy", "Borderline mycobacterium leprae infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "borderline leprosy", "shortest_name_length": 15}
{"curie": "UMLS:C0854989", "names": ["Lung squamous cell carcinoma recurrent", "Recurrent Squamous Cell Lung Carcinoma", "Recurrent Lung Squamous Cell Carcinoma", "Recurrent Squamous Cell Carcinoma of Lung", "Recurrent Squamous Cell Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung squamous cell carcinoma recurrent", "shortest_name_length": 38}
{"curie": "MONDO:0030931", "names": ["PRAAS4", "PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 4", "proteasome-associated autoinflammatory syndrome 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "proteasome-associated autoinflammatory syndrome 4", "shortest_name_length": 6}
{"curie": "MONDO:0006534", "names": ["Cholinergic urticaria", "Urticaria cholinergic", "cholinergic urticaria", "urticaria cholinergic", "cholinergic; urticaria", "URTICARIA, CHOLINERGIC", "urticaria; cholinergic", "Cholinergic urticaria (disorder)", "Cholinergic angio-edema-urticaria", "cholinergic urticaria (diagnosis)", "Cholinergic angio-oedema-urticaria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholinergic urticaria", "shortest_name_length": 21}
{"curie": "MONDO:0019480", "names": ["LCS", "Langerhans Cell Sarcoma", "sarcoma Langerhans cell", "Langerhans cell sarcoma", "Langerhans Cell Sarcomas", "Sarcoma, Langerhans Cell", "Sarcomas, Langerhans Cell", "sarcoma of Langerhans cell", "malignant Langerhans cell sarcoma", "Langerhans cell sarcoma (disorder)", "Langerhans cell sarcoma (diagnosis)", "Langerhans cell sarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Langerhans cell sarcoma", "shortest_name_length": 3}
{"curie": "MONDO:0018170", "names": ["NPHS2", "NEPHROTIC SYNDROME, TYPE 2", "Nephrotic Syndrome, Type 2", "idiopathic nephrotic syndrome", "Idiopathic Nephrotic Syndrome", "Idiopathic nephrotic syndrome", "Nephrotic Syndrome, Idiopathic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic nephrotic syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0021408", "names": ["frontal sinus polyp", "Frontal Sinus Polyp", "Frontal sinus polyp", "polyp; frontal sinus", "frontal sinus; polyp", "Polyp of frontal sinus", "polyp of frontal sinus", "Polyp of Frontal Sinus", "Polyp of the Frontal Sinus", "polyp of the frontal sinus", "Frontal sinus polyp (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyp of frontal sinus", "shortest_name_length": 19}
{"curie": "MONDO:0008810", "names": ["Apoc2 deficiency", "APOC2 DEFICIENCY", "Apo-c-II deficiency", "Anapolipoproteinemia", "Anapolipoproteinaemia", "Familial APOC2 deficiency", "C-II anapolipoproteinemia", "familial APOC2 deficiency", "C-II Anapolipoproteinemia", "C-II ANAPOLIPOPROTEINEMIA", "Anapolipoproteinemia, C-II", "C-II Anapolipoproteinemias", "Anapolipoproteinemias, C-II", "Familial apoC-II deficiency", "familial apoC-II deficiency", "Hyperlipoproteinemia Type Ib", "Type Ib Hyperlipoproteinemia", "Hyperlipoproteinemia, Type Ib", "hyperlipoproteinemia, type Ib", "Type Ib Hyperlipoproteinemias", "HYPERLIPOPROTEINEMIA, TYPE IB", "hyperlipoproteinemia, type 1b", "Hyperlipoproteinemia Type Ibs", "hyperlipoproteinemia, type 1B", "hyperlipoproteinemia, type IB", "APOLIPOPROTEIN C-II DEFICIENCY", "Hyperlipoproteinemias, Type Ib", "Apolipoprotein C II Deficiency", "apolipoprotein C-II deficiency", "Apolipoprotein C-II Deficiency", "Deficiency, Apolipoprotein C-II", "Apolipoprotein C-II Deficiencies", "Deficiencies, Apolipoprotein C-II", "familial apolipoprotein C-II deficiency", "Familial apolipoprotein C-II deficiency", "Apolipoprotein C-II Deficiency (disorder)", "Familial Fat-Induced Hypertriglyceridemia", "Familial Fat Induced Hypertriglyceridemia", "Fat-Induced Hypertriglyceridemia, Familial", "Hypertriglyceridemia, Familial Fat-Induced", "Familial Fat-Induced Hypertriglyceridemias", "Fat-Induced Hypertriglyceridemias, Familial", "Hypertriglyceridemias, Familial Fat-Induced", "Familial apolipoprotein C-II deficiency (disorder)", "familial apolipoprotein C-II deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial apolipoprotein C-II deficiency", "shortest_name_length": 16}
{"curie": "UMLS:C2987268", "names": ["Esophageal DLBCL", "Esophageal Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Diffuse Large B-Cell Lymphoma", "shortest_name_length": 16}
{"curie": "MONDO:0008680", "names": ["WT2", "FWT2", "Wilms tumor 2", "WILMS TUMOR 2", "Wilms tumor type 2", "familial Wilms tumor 2", "Familial Wilms tumor 2", "Wilms tumor 2, autosomal dominant, somatic mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wilms tumor 2", "shortest_name_length": 3}
{"curie": "MONDO:0022819", "names": ["congenital arteriovenous shunt"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital arteriovenous shunt", "shortest_name_length": 30}
{"curie": "UMLS:C1527424", "names": ["CIN 1", "cervical squamous intraepithelial neoplasia 1", "Cervical Squamous Intraepithelial Neoplasia 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Squamous Intraepithelial Neoplasia 1", "shortest_name_length": 5}
{"curie": "MONDO:0007957", "names": ["MEDIOSTERNAL DEPIGMENTATION LINE", "mediosternal depigmentation line"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mediosternal depigmentation line", "shortest_name_length": 32}
{"curie": "MONDO:0032621", "names": ["MC1DN16", "nuclear type mitochondrial complex I deficiency 16", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 16", "mitochondrial complex 1 deficiency, nuclear type 16"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 16", "shortest_name_length": 7}
{"curie": "MONDO:0700187", "names": ["FPH", "feline progressive histiocytosis", "Feline Progressive Histiocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "feline progressive histiocytosis", "shortest_name_length": 3}
{"curie": "UMLS:C1168219", "names": ["Extrahepatic bile duct cancer stage II", "Extrahepatic Bile Duct Cancer Stage II", "Stage II Extrahepatic Bile Duct Cancer", "stage II extrahepatic bile duct cancer", "Stage II Extrahepatic Bile Duct Carcinoma", "Stage II Carcinoma of Extrahepatic Bile Duct", "Stage II Carcinoma of the Extrahepatic Bile Duct"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extrahepatic bile duct cancer stage II", "shortest_name_length": 38}
{"curie": "MONDO:0019734", "names": ["JPM", "juvenile PM", "Juvenile PM", "Juvenile Polymyositis", "Juvenile polymyositis", "juvenile polymyositis", "Juvenile polymyositis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile polymyositis", "shortest_name_length": 3}
{"curie": "UMLS:C4688434", "names": ["Nodular Lymphocyte Predominant Hodgkin Lymphoma by Ann Arbor Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nodular Lymphocyte Predominant Hodgkin Lymphoma by Ann Arbor Stage", "shortest_name_length": 66}
{"curie": "UMLS:C0751692", "names": ["Multiple Hemangioblastoma", "Hemangioblastoma, Multiple", "Multiple Hemangioblastomas", "Hemangioblastomas, Multiple"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Multiple Hemangioblastomas", "shortest_name_length": 25}
{"curie": "UMLS:C4526857", "names": ["Recurrent Cervical Squamous Cell Cancer", "Relapsed Cervical Squamous Cell Carcinoma", "Recurrent Cervical Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Cervical Squamous Cell Carcinoma", "shortest_name_length": 39}
{"curie": "MONDO:0013955", "names": ["IMD30", "IL12RB1 deficiency", "IL12RB1 Deficiency", "IL12RB1 DEFICIENCY", "immunodeficiency 30", "IMMUNODEFICIENCY 30", "Immunodeficiency 30", "IL-12Râ1 deficiency", "immunodeficiency type 30", "IL-12 Receptor B Deficiency", "IL12RB1-Associated Immunodeficiency", "MSMD due to complete IL12RB1 deficiency", "MSMD due to complete interleukin 12 receptor beta 1 deficiency", "Mendelian susceptibility to interleukin 12 receptor beta 1 deficiency", "Mendelian susceptibility to mycobacterial infections due to IL12 deficiency", "Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency", "IL12RB1 autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency", "autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency caused by mutation in IL12RB1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0014695", "names": ["GLM9", "POT1 malignant glioma", "Pot1 malignant glioma", "glioma susceptibility 9", "GLIOMA SUSCEPTIBILITY 9", "glioma susceptibility type 9", "malignant glioma caused by mutation in POT1", "malignant glioma caused by mutation in Pot1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glioma susceptibility 9", "shortest_name_length": 4}
{"curie": "MONDO:0011258", "names": ["BOS1", "Bos1", "BO syndrome 1", "BO SYNDROME 1", "bo syndrome 1", "branchiootic dysplasia", "branchiootic syndrome 1", "Branchiootic Syndrome 1", "BRANCHIOOTIC SYNDROME 1", "EYA1 branchiootic syndrome", "branchiootic syndrome type 1", "branchiootic syndrome caused by mutation in EYA1", "anterior segment anomalies with or without cataract", "ANTERIOR SEGMENT ANOMALIES WITH OR WITHOUT CATARACT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "branchiootic syndrome 1", "shortest_name_length": 4}
{"curie": "MONDO:0001942", "names": ["gad", "GAD", "gads", "anxiety disorder generalize", "generalised anxiety disorder", "Generalized anxiety disorder", "Generalised anxiety disorder", "GENERALIZED ANXIETY DISORDER", "generalized anxiety disorder", "ANXIETY DISORDER GENERALIZED", "Generalized Anxiety Disorder", "anxiety disorder generalized", "anxiety disorders generalized", "generalized anxiety disorders", "anxiety disorder; generalized", "generalized; anxiety disorder", "GAD - Generalized anxiety disorder", "GAD - Generalised anxiety disorder", "Generalized anxiety disorder (disorder)", "generalized anxiety disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "generalized anxiety disorder", "shortest_name_length": 3}
{"curie": "MONDO:0015090", "names": ["autosomal recessive pure HSP", "autosomal recessive pure SPG", "autosomal recessive uncomplicated HSP", "autosomal recessive uncomplicated SPG", "autosomal recessive pure spastic paraplegia", "autosomal recessive uncomplicated spastic paraplegia", "autosomal recessive pure hereditary spastic paraplegia", "pure hereditary spastic paraplegia, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive pure spastic paraplegia", "shortest_name_length": 28}
{"curie": "UMLS:C0018036", "names": ["Goldblatt Syndrome", "Syndrome, Goldblatt", "Goldblatt hypertension", "Goldblatt Hypertension", "hypertension; Goldblatt", "Hypertension, Goldblatt", "Goldblatt; hypertension", "Goldblatt hypertension (disorder)", "Goldblatt hypertension (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypertension, Goldblatt", "shortest_name_length": 18}
{"curie": "MONDO:0002074", "names": ["Behcet syndrome arthropathy", "Arthropathy;Behcets syndrome", "Behcets syndrome arthropathy", "Behcet's syndrome arthropathy", "Arthropathy in Behcet syndrome", "Arthropathy in Behcet's syndrome", "Arthropathy in Behcet's Syndrome", "arthropathy in Behcet's syndrome", "Behcet's syndrome with arthropathy", "Arthropathy in Behcet's syndrome (disorder)", "Behcet's syndrome with arthropathy (diagnosis)", "Arthropathy in Behcet's syndrome involving hand", "arthropathy in Behcet's syndrome involving hand", "arthropathy in Behcet's syndrome involving forearm", "Arthropathy in Behcet's syndrome involving forearm", "Arthropathy in Behcet's syndrome, site unspecified", "arthropathy in Behcet's syndrome involving lower leg", "arthropathy in Behcet's syndrome involving upper arm", "Arthropathy in Behcet's syndrome involving upper arm", "Arthropathy in Behcet's syndrome involving lower leg", "Seronegative arthritis secondary to Behcet's syndrome", "Arthropathy in Behcet's syndrome involving multiple sites", "arthropathy in Behcet's syndrome involving multiple sites", "Arthropathy in Behcet's syndrome involving ankle and foot", "arthropathy in Behcet's syndrome involving ankle and foot", "Arthropathy in Behcet's syndrome involving shoulder region", "arthropathy in Behcet's syndrome involving shoulder region", "Arthropathy in Behcet's syndrome involving pelvic region and thigh", "arthropathy in Behcet's syndrome involving pelvic region and thigh"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Behcet syndrome arthropathy", "shortest_name_length": 27}
{"curie": "UMLS:C1336350", "names": ["Stage IVA Mouth Adenoid Cystic Carcinoma", "Stage IVA Oral Cavity Adenoid Cystic Cancer", "Stage IVA Adenoid Cystic Carcinoma of Mouth", "Stage IVA Oral Cavity Adenoid Cystic Carcinoma", "Stage IVA Adenoid Cystic Carcinoma of the Mouth", "Stage IVA Adenoid Cystic Carcinoma of Oral Cavity", "Stage IVA Adenoid Cystic Carcinoma of the Oral Cavity", "Stage IVA Oral Cavity Adenoid Cystic Carcinoma AJCC v7", "Stage IVA Oral Cavity Adenoid Cystic Carcinoma AJCC v6", "Stage IVA Oral Cavity Adenoid Cystic Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Oral Cavity Adenoid Cystic Carcinoma AJCC v6 and v7", "shortest_name_length": 40}
{"curie": "MONDO:0022700", "names": ["cerebral palsy spastic monoplegic", "spastic monoplegic cerebral palsy", "spastic monoplegia cerebral palsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral palsy spastic monoplegic", "shortest_name_length": 33}
{"curie": "MONDO:0018005", "names": ["spastic paraplegia-Paget disease of bone syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic paraplegia-Paget disease of bone syndrome", "shortest_name_length": 49}
{"curie": "UMLS:C1333979", "names": ["Hepatitis Virus-Related Hepatocellular Cancer", "Hepatitis Virus Related Hepatocellular Carcinoma", "Hepatitis Virus-Related Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatitis Virus-Related Hepatocellular Carcinoma", "shortest_name_length": 45}
{"curie": "UMLS:C1541449", "names": ["recurrent grade II lymphomatoid granulomatosis", "Recurrent Grade II Lymphomatoid Granulomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Grade II Lymphomatoid Granulomatosis", "shortest_name_length": 46}
{"curie": "MONDO:0019080", "names": ["total alopecia", "Total alopecia", "Alopecia, total", "alopecia totalis", "Alopecia totalis", "ALOPECIA TOTALIS", "totalis; alopecia", "alopecia; totalis", "total alopecia areata", "Total alopecia areata", "alopecia capitis totalis", "total baldness was noted", "Alopecia (capitis) totalis", "Alopecia totalis (disorder)", "alopecia totalis (diagnosis)", "total alopecia (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alopecia totalis", "shortest_name_length": 14}
{"curie": "MONDO:0009486", "names": ["Kcs", "KCS", "KCS1", "Kenny-Caffey Syndrome Type 1", "Kenny-Caffey syndrome type 1", "Kenny-Caffey syndrome, type 1", "Kenny-Caffey syndrome, Type 1", "KENNY-CAFFEY SYNDROME, TYPE 1", "Autosomal recessive Kenny-Caffey syndrome", "autosomal recessive Kenny-Caffey syndrome", "Kenny-Caffey Syndrome, Autosomal Recessive", "Kenny-Caffey syndrome, autosomal recessive", "KENNY-CAFFEY SYNDROME, AUTOSOMAL RECESSIVE", "Kenny-Caffey syndrome, autosomal recessive form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive Kenny-Caffey syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C1739366", "names": ["Injection site papule"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site papule", "shortest_name_length": 21}
{"curie": "UMLS:C0346973", "names": ["Metastasis to Large Bowel", "Large intestine metastases", "Metastases to large intestine", "Metastases to Large Intestine", "Metastasis to large intestine", "Metastasis to the Large Bowel", "Metastasis to the Large Intestine", "Cancer metastatic to large intestine", "Metastatic Tumor to the Large Intestine", "Metastatic Neoplasm to the Large Intestine", "large intestine neoplasm malignant secondary", "Secondary malignant neoplasm of large intestine", "Metastatic malignant neoplasm of large intestine", "Metastatic malignant neoplasm to large intestine", "Metastatic Malignant Neoplasm in the Large Intestine", "Secondary malignant neoplasm of large intestine, NOS", "Metastatic Malignant Neoplasm to the Large Intestine", "Metastatic malignant neoplasm to large intestine, NOS", "Secondary malignant neoplasm of large intestine (diagnosis)", "Metastatic malignant neoplasm to large intestine (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to large intestine", "shortest_name_length": 25}
{"curie": "UMLS:C5419466", "names": ["Recurrent Myeloid Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Myeloid Neoplasm", "shortest_name_length": 26}
{"curie": "MONDO:0000460", "names": ["neural glioblastoma", "Neural Glioblastoma", "glioblastoma neural subtype"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neural glioblastoma", "shortest_name_length": 19}
{"curie": "MONDO:0014005", "names": ["AHUS7", "NPHS7", "Ig-mediated MPGN", "AHUS, SUSCEPTIBILITY TO, 7", "Ahus, susceptibility to, 7", "nephrotic syndrome, type 7", "NEPHROTIC SYNDROME, TYPE 7", "Immunoglobulin-mediated MPGN", "Mesangiocapillary Glomerulonephritis Type 1", "Mesangiocapillary glomerulonephritis type I", "Mesangiocapillary glomerulonephritis type 1", "Mesangiocapillary glomerulonephritis, type I", "Mesangiocapillary Glomerulonephritis, Type I", "Membranoproliferative Glomerulonephritis Type I", "membranoproliferative glomerulonephritis type I", "Membranoproliferative Glomerulonephritis, Type I", "Glomerulonephritis, membranoproliferative, Type I", "Subendothelial mesangiocapillary glomerulonephritis", "Ig-mediated membranoproliferative glomerulonephritis", "Subendothelial Membranoproliferative Glomerulonephritis", "Mesangiocapillary glomerulonephritis, type I (disorder)", "Membranoproliferative Glomerulonephritis, Subendothelial", "Mesangiocapillary glomerulonephritis, type I (diagnosis)", "MCGN type I - Mesangiocapillary glomerulonephritis type I", "HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 7", "hemolytic uremic syndrome, atypical, susceptibility to, 7", "Immune Complex Mediated Membranoproliferative Glomerulonephritis", "immune Complex mediated membranoproliferative glomerulonephritis", "immunoglobulin-mediated membranoproliferative glomerulonephritis", "NEPHROTIC SYNDROME, TYPE 7, WITH MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS", "nephrotic syndrome, type 7, with membranoproliferative glomerulonephritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunoglobulin-mediated membranoproliferative glomerulonephritis", "shortest_name_length": 5}
{"curie": "UMLS:C4050012", "names": ["Transsphincteric", "Sphincteric Ureterocele"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sphincteric Ureterocele", "shortest_name_length": 16}
{"curie": "MONDO:0002544", "names": ["brain oligodendroglioma", "Brain Oligodendroglioma", "Oligodendroglioma of Brain", "Oligodendroglioma of brain", "oligodendroglioma of brain", "oligodendroglioma of the brain", "Oligodendroglioma of the Brain", "malignant oligodendroglioma of brain", "Oligodendroglioma of brain (disorder)", "malignant oligodendroglioma of brain (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brain oligodendroglioma", "shortest_name_length": 23}
{"curie": "MONDO:0005866", "names": ["DMAC", "MAC disease", "Bacillus; Battey", "Mycobacterium avium Complex", "Mycobacterium avium infection", "Infection mycobacterium avium", "Mycobacterium; intracellulare", "intracellulare; Mycobacterium", "Mycobacterium Avium Infection", "mycobacterium avium complex disease", "Mycobacterium avium complex disease", "MYCOBACTERIUM AVIUM COMPLEX INFECTION", "Mycobacterium avium complex infection", "Mycobacterium intracellulare Infection", "Mycobacterium intracellulare infection", "Infection, Mycobacterium intracellulare", "Mycobacterium intracellulare Infections", "Infections, Mycobacterium intracellulare", "Mycobacterium avium intracellulare Infection", "Mycobacterium avium-intracellulare Infection", "Mycobacterium avium intracellulare infection", "MYCOBACTERIUM AVIUM-INTRACELLULARE INFECTION", "Infection, Mycobacterium avium-intracellulare", "Mycobacterium avium-intracellulare Infections", "Infection due to Mycobacterium intracellulare", "infection due to Mycobacterium intracellulare", "Infection, Mycobacterium avium intracellulare", "Mycobacterium avium complex infectious disease", "Infections, Mycobacterium avium-intracellulare", "Mycobacterium avium complex disease or disorder", "Infection caused by Mycobacterium intracellulare", "Mycobacterium avium-intracellulare complex infection", "Mycobacterium avium complex caused disease or disorder", "disseminated infection with mycobacterium avium complex", "Infection caused by Mycobacterium intracellulare (disorder)", "Mycobacterium avium-intracellulare complex infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mycobacterium avium complex disease", "shortest_name_length": 4}
{"curie": "MONDO:0014123", "names": ["CILD21", "primary ciliary dyskinesia 21", "CILIARY DYSKINESIA, PRIMARY, 21", "ciliary dyskinesia, primary, 21", "DRC1 primary ciliary dyskinesia", "primary ciliary dyskinesia type 21", "ciliary dyskinesia, primary, type 21", "primary ciliary dyskinesia 21 without situs inversus", "primary ciliary dyskinesia caused by mutation in DRC1", "CILIARY DYSKINESIA, PRIMARY, 21, WITHOUT SITUS INVERSUS", "ciliary dyskinesia, primary, 21, without situs inversus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia 21", "shortest_name_length": 6}
{"curie": "UMLS:C0948268", "names": ["hemodynamic instability", "Hemodynamic Instability", "Hemodynamic instability", "Haemodynamic instability", "hemodynamics instability", "Hemodynamic instability (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemodynamic instability", "shortest_name_length": 23}
{"curie": "MONDO:0002061", "names": ["Intraductal Papillary Breast Neoplasm", "intraductal papillary breast neoplasm", "Breast Intraductal Papillary Neoplasm", "Intraductal papillary breast neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intraductal papillary breast neoplasm", "shortest_name_length": 37}
{"curie": "MONDO:0100481", "names": ["active TB", "active tuberculosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "active tuberculosis", "shortest_name_length": 9}
{"curie": "UMLS:C4724969", "names": ["Refractory Round Cell Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Round Cell Liposarcoma", "shortest_name_length": 33}
{"curie": "UMLS:C1511262", "names": ["Borderline Ovarian Endometrioid Adenofibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Ovarian Endometrioid Adenofibroma", "shortest_name_length": 44}
{"curie": "MONDO:0008766", "names": ["Amaurosis hypertrichosis", "Amaurosis-hypertrichosis syndrome", "Amaurosis hypertrichosis syndrome", "amaurosis-hypertrichosis syndrome", "Amaurosis hypertrichosis syndrome (disorder)", "amaurosis congenita cone-rod type with congenital hypertrichosis", "Congenital amaurosis cone-rod type with congenital hypertrichosis", "AMAUROSIS CONGENITA, CONE-ROD TYPE, WITH CONGENITAL HYPERTRICHOSIS", "Amaurosis Congenita, Cone-Rod Type, with Congenital Hypertrichosis", "amaurosis congenita, cone-rod type, with congenital hypertrichosis", "Cone-rod congenital amaurosis associated with congenital hypertrichosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amaurosis-hypertrichosis syndrome", "shortest_name_length": 24}
{"curie": "MONDO:0016484", "names": ["USH2", "Usher Syndrome Type 2", "Usher syndrome type 2", "Usher syndrome type 2 (disorder)", "Usher syndrome type 2 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Usher syndrome type 2", "shortest_name_length": 4}
{"curie": "UMLS:C2103415", "names": ["Basal Ganglia Neoplasm", "neoplasm of basal ganglia", "neoplasm of basal ganglia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplasm of basal ganglia", "shortest_name_length": 22}
{"curie": "MONDO:0010380", "names": ["CASM Syndrome", "CASM SYNDROME", "Casm syndrome", "cataract, ataxia, short stature, and mental retardation", "Cataract, Ataxia, Short Stature, And Mental Retardation", "CATARACT, ATAXIA, SHORT STATURE, AND MENTAL RETARDATION", "Cataracts, ataxia, short stature, and mental retardation", "cataracts, ataxia, short stature, and mental retardation", "cataract, ataxia, short stature, and intellectual disability", "cataracts, ataxia, short stature, and intellectual disability", "CATARACT, ATAXIA, SHORT STATURE, AND IMPAIRED INTELLECTUAL DEVELOPMENT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract, ataxia, short stature, and intellectual disability", "shortest_name_length": 13}
{"curie": "MONDO:0017876", "names": ["Guanarito hemorrhagic fever", "Guanarito haemorrhagic fever", "Venezuelan hemorrhagic fever", "Venezuelan haemorrhagic fever", "Venezuelan hemorrhagic fever (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Venezuelan hemorrhagic fever", "shortest_name_length": 27}
{"curie": "MONDO:0019261", "names": ["INCL", "Infantile NCL", "infantile NCL", "Santavuori disease", "SANTAVUORI DISEASE", "Santavuori Disease", "SANTAVUORI-HALTIA DISEASE", "Santavuori-Haltia disease", "Santavuori-Haltia Disease", "Santavuori Haltia Disease", "Hagberg-Santavuori disease", "Polyunsaturated acid lipidosis", "Polyunsaturated fatty acid lipidosis", "Neuronal Ceroid Lipofuscinosis Type 1", "infantile neuronal ceroid lipofuscinosis", "Infantile Neuronal Ceroid Lipofuscinosis", "Infantile neuronal ceroid lipofuscinosis", "NEURONAL CEROID LIPOFUSCINOSIS, INFANTILE", "Neuronal Ceroid Lipofuscinosis, Infantile", "Ceroid lipofuscinosis, neuronal 1, infantile", "Infantile neuronal ceroid lipofuscinosis (disorder)", "Haltia-Santavouri type neuronal ceroid lipofuscinosis", "Neuronal ceroid lipofuscinosis infantile Finnish type", "Neuronal ceroid lipofuscinosis, infantile Finnish type", "Hagberg-Santavouri type neuronal ceroid lipofuscinosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile neuronal ceroid lipofuscinosis", "shortest_name_length": 4}
{"curie": "MONDO:0044727", "names": ["pancreatic MiNEN", "MiNEN of pancreas", "Pancreatic Mixed Adenoneuroendocrine Carcinoma", "Pancreatic Carcinoma with Mixed Differentiation", "pancreatic carcinoma with mixed differentiation", "Mixed Exocrine-Endocrine Carcinoma of the Pancreas", "mixed exocrine-endocrine carcinoma of the pancreas", "Mixed pancreatic endocrine and exocrine tumor, malignant", "pancreatic mixed neuroendocrine-nonneuroendocrine neoplasm", "mixed neuroendocrine-nonneuroendocrine neoplasm of pancreas", "Pancreatic Mixed Neuroendocrine-Non-Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic carcinoma with mixed differentiation", "shortest_name_length": 16}
{"curie": "MONDO:0033198", "names": ["DFNB106", "deafness autosomal recessive 106", "DEAFNESS, AUTOSOMAL RECESSIVE 106", "deafness, autosomal recessive 106", "hearing loss, autosomal recessive 106", "autosomal recessive nonsyndromic deafness 106"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal recessive 106", "shortest_name_length": 7}
{"curie": "UMLS:C0153251", "names": ["candidiasis lung", "lung candidiasis", "candidiasis lungs", "Candidosis of lung", "Candidal pneumonia", "candidiasis of lung", "Candidiasis of lung", "MONILIASIS PULMONARY", "Moniliasis pulmonary", "Pulmonary candidosis", "candidiasis pulmonary", "PULMONARY CANDIDIASIS", "Pulmonary candidiasis", "candidiasis pneumonia", "pulmonary candidiasis", "RESPIRATORY MONILIASIS", "CANDIDIASIS, PULMONARY", "Respiratory moniliasis", "Candidiasis respiratory", "respiratory candidiasis", "MONILIASIS RESPIRATORY SYSTEM", "Moniliasis respiratory system", "Candidiasis of lung (disorder)", "candidiasis pneumonia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Candidiasis of lung", "shortest_name_length": 16}
{"curie": "UMLS:C4528753", "names": ["Stage IIA Colon Neuroendocrine Tumor", "Stage IIA Colon Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Colon Neuroendocrine Tumor AJCC v8", "shortest_name_length": 36}
{"curie": "MONDO:0012411", "names": ["GAN2", "CMT2 with giant axons", "HMSN2 with giant axons", "giant axonal neuropathy 2", "DCAF8 giant axonal neuropathy", "giant axonal neuropathy type 2", "Giant Axonal Neuropathy, Autosomal Dominant", "giant axonal neuropathy 2, autosomal dominant", "GIANT AXONAL NEUROPATHY 2, AUTOSOMAL DOMINANT", "giant axonal neuropathy caused by mutation in DCAF8", "autosomal dominant Charcot-Marie-Tooth disease type 2 with giant axons", "autosomal dominant hereditary motor and sensory neuropathy type 2 with giant axons"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "giant axonal neuropathy 2", "shortest_name_length": 4}
{"curie": "MONDO:0024537", "names": ["RTD2", "BVVLS1", "pontobulbar palsy with deafness", "Pontobulbar Palsy With Deafness", "PONTOBULBAR PALSY WITH DEAFNESS", "Brown-Vialetto-Van Laere syndrome", "BROWN-VIALETTO-VAN LAERE SYNDROME 1", "Riboflavin transporter deficiency 2", "Brown-Vialetto-van Laere syndrome 1", "Brown-Vialetto-Van Laere Syndrome 1", "Brown-Vialetto-Van Laere syndrome 1", "SLC52A3 Brown-Vialetto-van Laere syndrome", "Pontobulbar palsy and neurosensory deafness", "RFVT2-related riboflavin transporter deficiency", "rfvt2-related riboflavin transporter deficiency", "Progressive Bulbar Palsy with Sensorineural Deafness", "Bulbar Palsy, Progressive, with Sensorineural Deafness", "bulbar palsy, progressive, with sensorineural deafness", "BULBAR PALSY, PROGRESSIVE, WITH SENSORINEURAL DEAFNESS", "Bulbar Palsy, Progressive, With Sensorineural Deafness", "Brown-Vialetto-van Laere syndrome caused by mutation in SLC52A3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brown-Vialetto-van Laere syndrome 1", "shortest_name_length": 4}
{"curie": "UMLS:C4682751", "names": ["IIC", "stage IIC prostate cancer", "Stage IIC Prostate Cancer", "Stage IIC Prostate Cancer AJCC v8", "stage IIC prostate cancer AJCC v8", "stage IIC prostate carcinoma AJCC v8", "Stage IIC Prostate Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIC Prostate Cancer AJCC v8", "shortest_name_length": 3}
{"curie": "UMLS:C1963864", "names": ["Myelodysplastic syndrome transformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myelodysplastic syndrome transformation", "shortest_name_length": 39}
{"curie": "MONDO:0033532", "names": ["SULEHS", "SULEIMAN-EL-HATTAB SYNDROME", "Suleiman-El-Hattab syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Suleiman-El-Hattab syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0008038", "names": ["ATXPC", "Myelocerebellar disorder", "MYELOCEREBELLAR DISORDER", "Myelocerebellar Disorder", "myelocerebellar disorder", "ataxia-pancytopenia syndrome", "Ataxia pancytopenia syndrome", "Ataxia-Pancytopenia Syndrome", "Ataxia-pancytopenia syndrome", "ATAXIA-PANCYTOPENIA SYNDROME", "pancytopenia autoimmune ataxia", "Ataxia pancytopenia syndrome (disorder)", "Ataxia pancytopenia syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ataxia-pancytopenia syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C1504444", "names": ["Implant site cellulitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Implant site cellulitis", "shortest_name_length": 23}
{"curie": "MONDO:0012999", "names": ["CCDS2", "GAMT DEFICIENCY", "GAMT deficiency", "GAMT Deficiency", "cerebral creatine deficiency syndrome 2", "Cerebral Creatine Deficiency Syndrome 2", "CEREBRAL CREATINE DEFICIENCY SYNDROME 2", "Cerebral creatine deficiency syndrome 2", "cerebral creatine deficiency syndrome type 2", "guanidinoacetate methyltransferase deficiency", "GUANIDINOACETATE METHYLTRANSFERASE DEFICIENCY", "Guanidinoacetate Methyltransferase Deficiency", "Guanidinoacetate methyltransferase deficiency", "Deficiency of guanidinoacetate methyltransferase", "creatine deficiency syndrome due to GAMT deficiency", "Creatine Deficiency Syndrome Due To Gamt Deficiency", "CREATINE DEFICIENCY SYNDROME DUE TO GAMT DEFICIENCY", "guanidinoacetate N-methyltransferase activity disease", "disorder of guanidinoacetate N-methyltransferase activity", "Deficiency of guanidinoacetate methyltransferase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "guanidinoacetate methyltransferase deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0013628", "names": ["MRT17", "MRT21", "GPIBD8", "HPMRS3", "mental retardation, autosomal recessive 21", "mental retardation, autosomal recessive 17", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 17", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 21", "intellectual disability, autosomal recessive 21", "intellectual disability, autosomal recessive 17", "glycosylphosphatidylinositol biosynthesis defect 8", "GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 8", "hyperphosphatasia with mental retardation syndrome 3", "PGAP2 hyperphosphatasia-intellectual disability syndrome", "hyperphosphatasia with mental retardation syndrome type 3", "hyperphosphatasia with intellectual disability syndrome 3", "HYPERPHOSPHATASIA WITH INTELLECTUAL DEVELOPMENTAL DISORDER 3", "hyperphosphatasia with intellectual disability syndrome type 3", "hyperphosphatasia with impaired intellectual development syndrome 3", "HYPERPHOSPHATASIA WITH IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME 3", "hyperphosphatasia-intellectual disability syndrome caused by mutation in PGAP2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperphosphatasia with intellectual disability syndrome 3", "shortest_name_length": 5}
{"curie": "UMLS:C0334067", "names": ["NOF", "Non-Ossifying Fibroma", "fibroma non ossifying", "non-ossifying fibroma", "Non-ossifying fibroma", "fibromas non ossifying", "metaphyseal fibrous defect", "Metaphyseal fibrous defect", "BONE FIBROUS CORTICAL DEFECT", "Fibrous cortical defect, bone", "Fibrous cortical defect of bone", "Metaphyseal fibrous defect (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Ossifying Fibroma", "shortest_name_length": 3}
{"curie": "UMLS:C0264395", "names": ["MacLeod", "macleod syndrome", "MacLeod Syndrome", "MacLeods syndrome", "Syndrome, MacLeod", "macleods syndrome", "macleod's syndrome", "MacLeod's syndrome", "Swyer-James syndrome", "Unilateral emphysema", "Swyer James Syndrome", "Swyer-James Syndrome", "swyer-james syndrome", "swyer james syndrome", "Emphysema, unilateral", "unilateral; emphysema", "Syndrome, Swyer-James", "emphysema; unilateral", "Unilateral hyperlucent lung", "Unilateral emphysema syndrome", "MacLeod's unilateral emphysema", "Unilateral hyperlucent lung syndrome", "Lung or pulmonary emphysema, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Swyer-James Syndrome", "shortest_name_length": 7}
{"curie": "MONDO:0002168", "names": ["Rectal Sarcoma", "rectal sarcoma", "rectum sarcoma", "sarcoma of rectum", "Sarcoma of Rectum", "sarcoma of the rectum", "Sarcoma of the Rectum", "sarcoma of rectum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rectum sarcoma", "shortest_name_length": 14}
{"curie": "MONDO:0001238", "names": ["Plethora of newborn", "plethora of newborn", "Neonatal polycythemia", "Neonatal Polycythemia", "neonatal polycythemia", "Neonatal polycythaemia", "Polycythemia, neonatal", "Polycythemia neonatorum", "Polycythemia Neonatorum", "polycythemia neonatorum", "Polycythaemia neonatorum", "polycythemia; neonatorum", "neonatorum; polycythemia", "polycythemia of the newborn", "Polycythemia of the Newborn", "NEONATAL POLYCYTHEMIA SYNDROME", "Neonatal polycythemia (disorder)", "neonatal polycythemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polycythemia neonatorum", "shortest_name_length": 19}
{"curie": "MONDO:0008745", "names": ["ATN", "OCA1A", "albinism 1", "Albinism I", "Tyr oculocutaneous albinism", "TYR oculocutaneous albinism", "Oculocutaneous albinism ty-neg", "Oculocutaneous Albinism Type 1A", "oculocutaneous albinism, type 1", "oculocutaneous albinism type 1a", "oculocutaneous albinism type 1A", "Oculocutaneous albinism type 1A", "oculocutaneous albinism type IA", "Albinism, Oculocutaneous, Type IA", "ALBINISM, OCULOCUTANEOUS, TYPE IA", "albinism, oculocutaneous, type 1A", "albinism, oculocutaneous, type IA", "Tyrosinase-related oculocutaneous albinism", "Tyrosinase-negative oculocutaneous albinism", "tyrosinase-negative oculocutaneous albinism", "oculocutaneous albinism type 1a (diagnosis)", "oculocutaneous albinism tyrosinase-negative", "Tyrosinase negative oculocutaneous albinism", "Oculocutaneous Albinism, Tyrosinase-Negative", "Oculocutaneous albinism, tyrosinase negative", "OCULOCUTANEOUS ALBINISM, TYROSINASE-NEGATIVE", "oculocutaneous albinism, tyrosinase-negative", "oculocutaneous albinism caused by mutation in TYR", "oculocutaneous albinism caused by mutation in Tyr", "OCA1 - Tyrosinase-negative oculocutaneous albinism", "Tyrosinase-negative oculocutaneous albinism (disorder)", "Tyrosinase-negative oculocutaneous albinism (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculocutaneous albinism type 1A", "shortest_name_length": 3}
{"curie": "MONDO:0024235", "names": ["brenner tumor", "Brenner tumor", "Brenner Tumor", "brenner tumors", "Brenner tumour", "brenner tumour", "Brenner tumor, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brenner tumor", "shortest_name_length": 13}
{"curie": "UMLS:C5446577", "names": ["Conjunctival Rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conjunctival Rhabdomyosarcoma", "shortest_name_length": 29}
{"curie": "MONDO:0001947", "names": ["abscess of thyroid", "Pyogenic thyroiditis", "pyogenic thyroiditis", "pyogenic; thyroiditis", "thyroiditis; pyogenic", "thyroiditis infectious", "Infectious Thyroiditis", "infectious thyroiditis", "Infectious thyroiditis", "suppurative thyroiditis", "Thyroiditis, Infectious", "Suppurative Thyroiditis", "Suppurative thyroiditis", "suppurative; thyroiditis", "thyroiditis; suppurative", "Thyroiditis, Suppurative", "Infectious Thyroiditides", "Thyroiditides, Infectious", "Suppurative Thyroiditides", "Thyroiditides, Suppurative", "THYROIDITIS ACUTE PYOGENIC", "Infectious thyroiditis, NOS", "Acute Infectious Thyroiditis", "acute suppurative thyroiditis", "Thyroiditis, Acute Infectious", "Acute suppurative thyroiditis", "Infectious Thyroiditis, Acute", "Acute Suppurative Thyroiditis", "THYROIDITIS, ACUTE SUPPURATIVE", "Acute Infectious Thyroiditides", "Suppurative Thyroiditis, Acute", "Thyroiditis, Acute Suppurative", "Infectious Thyroiditides, Acute", "Acute Suppurative Thyroiditides", "Thyroiditides, Acute Infectious", "Thyroiditides, Acute Suppurative", "Suppurative Thyroiditides, Acute", "pyogenic thyroiditis (diagnosis)", "Infectious thyroiditis (disorder)", "Infectious thyroiditis (diagnosis)", "Acute suppurative thyroiditis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "suppurative thyroiditis", "shortest_name_length": 18}
{"curie": "MONDO:0005660", "names": ["Avulavirus Infection", "Infection, Avulavirus", "Avulavirus Infections", "Infections, Avulavirus", "Avulavirus infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Avulavirus infectious disease", "shortest_name_length": 20}
{"curie": "MONDO:0017278", "names": ["APS", "PGA", "pga", "aps", "Lloyd's syndrome", "lloyd's syndrome", "endocrine Lloyd's syndrome", "Lloyd's syndrome (diagnosis)", "Autoimmune Polyendocrinopathy", "autoimmune polyendocrinopathy", "Autoimmune polyendocrinopathy", "Polyendocrinopathy, Autoimmune", "polyendocrine failure syndrome", "Polyendocrinopathies, Autoimmune", "Autoimmune polyglandular failure", "autoimmune polyglandular failure", "Autoimmune Polyglandular Syndrome", "autoimmune polyendocrine syndrome", "Polyglandular Autoimmune Syndrome", "Autoimmune Polyendocrine Syndrome", "Polyglandular autoimmune syndrome", "autoimmune polyglandular syndrome", "Autoimmune polyglandular syndrome", "autoimmune; polyglandular syndrome", "Autoimmune polyendocrinopathy, NOS", "syndrome; autoimmune polyglandular", "Polyendocrine autoimmunity syndrome", "syndrome; polyglandular, autoimmune", "polyglandular; syndrome, autoimmune", "autoimmune polyglandular syndrome(s)", "Autoimmune Polyglandular Syndrome(s)", "polyglandular; deficiency, autoimmune", "deficiency; polyglandular, autoimmune", "Autoimmune Polyendocrinopathy Syndrome", "autoimmune polyendocrinopathy syndrome", "Polyglandular autoimmune syndrome, NOS", "Autoimmune polyglandular syndrome, NOS", "Autoimmune polyendocrinopathy (disorder)", "polyendocrine failure syndrome (diagnosis)", "autoimmune polyendocrine syndrome (diagnosis)", "autoimmune polyendocrine syndrome; polyglandular autoimmune syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune polyendocrinopathy", "shortest_name_length": 3}
{"curie": "MONDO:0009468", "names": ["IIH", "Nonne's syndrome", "nonne's syndrome", "Symond's syndrome", "Winke's meningitis", "HYDROPS, MENINGEAL", "Bornier's syndrome", "cerebri pseudotumor", "Pseudotumor Cerebri", "pseudotumor cerebri", "PSEUDOTUMOR CEREBRI", "Pseudotumor cerebri", "pseudotumour cerebri", "pseudotumor; cerebri", "Pseudotumour cerebri", "cerebri; pseudotumor", "benign intracran. hypt.", "Pseudotumor cerebri syndrome", "syndrome pseudotumor cerebri", "Otitic hydrocephalus syndrome", "Noninfective serous meningitis", "REDUCED CSF ABSORPTION SYNDROME", "benign intracranial hypertension", "Benign Intracranial Hypertension", "Benign intracranial hypertension", "benign hypertension intracranial", "BENIGN INTRACRANIAL HYPERTENSION", "Serous meningitis, non-infective", "INTRACRANIAL PRESSURE INC. BENIGN", "HYPERTENSION, INTRACRANIAL BENIGN", "Hypertension, Benign Intracranial", "Intracranial Hypertension, Benign", "Idiopathic Intracranial Hypertension", "Idiopathic intracranial hypertension", "idiopathic intracranial hypertension", "intracranial hypertension, idiopathic", "Intracranial Hypertension, Idiopathic", "Hypertension, Idiopathic Intracranial", "INTRACRANIAL HYPERTENSION, IDIOPATHIC", "BIH - Benign intracranial hypertension", "Benign intracranial hypertension syndrome", "intracranial; increased pressure (benign)", "IIH - Idiopathic intracranial hypertension", "increased; pressure, intracranial (benign)", "Benign intracranial hypertension (disorder)", "idiopathic intracranial hypertension (diagnosis)", "PSEUDOTUMOR CEREBRI BENIGN INTRACRANIAL HYPERTENSION", "PSEUDOTUMOR CEREBRI <BENIGN INTRACRANIAL HYPERTENSION>"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudotumor cerebri", "shortest_name_length": 3}
{"curie": "MONDO:0000503", "names": ["bronchioalveolar carcinoma", "lung adenocarcinoma in situ", "Lung Adenocarcinoma In Situ", "lung adenocarcinoma In situ", "bronchioloalveolar carcinoma", "Bronchioloalveolar Carcinoma", "pulmonary adenocarcinoma in situ", "in situ pulmonary adenocarcinoma", "stage 0 adenosquamous lung cancer", "Adenosquamous cell lung cancer stage 0", "lung adenosquamous cell carcinoma in situ", "stage 0 adenosquamous cell lung carcinoma", "adenosquamous cell carcinoma in situ of lung", "stage 0 adenosquamous cell carcinoma of lung", "stage 0 adenosquamous lung carcinoma aJCC v7", "stage 0 adenosquamous lung carcinoma aJCC v6", "stage 0 adenosquamous cell carcinoma of the lung", "adenosquamous cell carcinoma in situ of the lung", "stage 0 adenosquamous lung carcinoma aJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung adenocarcinoma in situ", "shortest_name_length": 26}
{"curie": "MONDO:0004108", "names": ["diaphragm sellae meningioma", "Diaphragm Sellae Meningioma", "diaphragma sellae meningioma", "Diaphragma Sellae Meningioma", "meningioma of Diaphragm Sellae", "Meningioma of Diaphragm Sellae", "meningioma of diaphragm sellae", "Meningioma of Diaphragma Sellae", "meningioma of Diaphragma sellae", "meningioma of the diaphragm sellae", "Meningioma of the Diaphragm Sellae", "Meningioma of the Diaphragma Sellae", "meningioma of the Diaphragma sellae", "diaphragma sellae meningioma (disease)", "meningioma (disease) of diaphragma sellae"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diaphragma sellae meningioma", "shortest_name_length": 27}
{"curie": "UMLS:C3897524", "names": ["Stage IV Anaplastic Large Cell Lymphoma", "Stage IV Childhood Anaplastic Large Cell Lymphoma", "stage IV childhood anaplastic large cell lymphoma", "Ann Arbor Stage IV Childhood Anaplastic Large Cell Lymphoma", "Ann Arbor Stage IV Noncutaneous Childhood Anaplastic Large Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Childhood Anaplastic Large Cell Lymphoma", "shortest_name_length": 39}
{"curie": "UMLS:C4708167", "names": ["Anemia due to and following chemotherapy", "Anaemia due to and following chemotherapy", "Anemia due to and following chemotherapy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anemia due to and following chemotherapy", "shortest_name_length": 40}
{"curie": "UMLS:C3544358", "names": ["Post-injection delirium/sedation syndrome", "Post-injection delirium sedation syndrome", "PDSS - post-injection delirium sedation syndrome", "Post-injection delirium sedation syndrome (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post-injection delirium sedation syndrome", "shortest_name_length": 41}
{"curie": "MONDO:0003405", "names": ["Adult CNS Germ Cell Tumor", "adult CNS germ cell tumor", "Germ Cell Tumor of Adult CNS", "germ cell tumor of adult CNS", "adult CNS germ cell neoplasm", "Adult CNS Germ Cell Neoplasm", "Germ Cell Neoplasm of Adult CNS", "germ cell neoplasm of adult CNS", "germ cell tumor of the adult CNS", "Germ Cell Tumor of the Adult CNS", "germ cell tumour of the adult CNS", "germ cell neoplasm of the adult CNS", "Germ Cell Neoplasm of the Adult CNS", "central nervous system germ cell tumor", "Central Nervous System Germ Cell Tumor", "central nervous system adult germ cell tumor", "Adult Central Nervous System Germ Cell Tumor", "adult central nervous system germ cell tumor", "central nervous system adult germ cell tumour", "germ cell tumor of adult central nervous system", "Germ Cell Tumor of Adult Central Nervous System", "Adult Central Nervous System Germ Cell Neoplasm", "adult central nervous system germ cell neoplasm", "central nervous system germ cell tumor of adults", "germ cell neoplasm of adult central nervous system", "Germ Cell Neoplasm of Adult Central Nervous System", "Germ Cell Tumor of the Adult Central Nervous System", "germ cell tumor of the adult central nervous system", "Germ Cell Neoplasm of the Adult Central Nervous System", "germ cell neoplasm of the adult central nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult central nervous system germ cell tumor", "shortest_name_length": 25}
{"curie": "MONDO:0002769", "names": ["LEUKORRHEA", "leukorrhea", "Leukorrhea", "LEUKORRHOEA", "leukorrhoea", "leucorrhoea", "Leucorrhoea", "Leukorrheas", "Leukorrhoea", "Leukorrhagia", "Leukorrhea NOS", "Leukorrhea, NOS", "leukorrhea of vagina", "Leukorrhea (finding)", "Leukorrhea of vagina", "discharge - leukorrhea", "white vaginal discharge", "VAGINAL DISCHARGE WHITE", "vaginal white discharge", "White vaginal discharge", "Vaginal discharge white", "discharge vaginal white", "Leukorrhea NOS of vagina", "White vaginal discharge (finding)", "white vaginal discharge (symptom)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukorrhea", "shortest_name_length": 10}
{"curie": "MONDO:0030438", "names": ["PCH16", "pontocerebellar hypoplasia type 16", "PONTOCEREBELLAR HYPOPLASIA, TYPE 16", "pontocerebellar hypoplasia, type 16"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pontocerebellar hypoplasia, type 16", "shortest_name_length": 5}
{"curie": "UMLS:C0343898", "names": ["Acute pulmonary histoplasmosis", "acute pulmonary histoplasmosis", "Acute pulmonary classical histoplasmosis", "Acute pulmonary histoplasmosis capsulati", "Acute pulmonary histoplasmosis (disorder)", "acute pulmonary histoplasmosis (diagnosis)", "histoplasmosis; Histoplasma capsulatum, pulmonary, acute (etiology)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute pulmonary histoplasmosis", "shortest_name_length": 30}
{"curie": "MONDO:0032838", "names": ["NEDMABA", "neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies", "NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ARTHROGRYPOSIS, AND STRUCTURAL BRAIN ANOMALIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies", "shortest_name_length": 7}
{"curie": "MONDO:0018383", "names": ["genetic osteonecrosis", "bone necrosis of genetic origin", "osteonecrosis of genetic origin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteonecrosis of genetic origin", "shortest_name_length": 21}
{"curie": "UMLS:C2827436", "names": ["Cystic Fibrosis Liver Disease", "Liver Disease Associated with Cystic Fibrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liver Disease Associated with Cystic Fibrosis", "shortest_name_length": 29}
{"curie": "UMLS:C4744833", "names": ["Recurrent Primary Peritoneal Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Primary Peritoneal Serous Adenocarcinoma", "shortest_name_length": 50}
{"curie": "UMLS:C0078921", "names": ["Tyrosinase-Negative Albinism", "tyrosinase-negative albinism", "tyrosinase negative albinism", "Albinism, tyrosinase negative", "Albinism, Tyrosinase Negative", "Albinism, Tyrosinase-Negative"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Albinism, Tyrosinase-Negative", "shortest_name_length": 28}
{"curie": "UMLS:C1335388", "names": ["Peripheral Intraneural Angiosarcoma", "Peripheral Intraneural Hemangiosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peripheral Intraneural Angiosarcoma", "shortest_name_length": 35}
{"curie": "MONDO:0013878", "names": ["PFBMFT1", "pulmonary fibrosis and/or bone marrow failure, telomere-related, 1", "pulmonary fibrosis and/or bone marrow failure, TELOMERE-RELATED, 1", "pulmonary fibrosis and/or bone marrow failure, Telomere-related, 1", "PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1", "TERT pulmonary fibrosis and/or bone marrow failure, Telomere-related", "pulmonary fibrosis and/or bone marrow failure, Telomere-related, type 1", "pulmonary fibrosis and/or bone marrow failure, Telomere-related caused by mutation in TERT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary fibrosis and/or bone marrow failure, Telomere-related, 1", "shortest_name_length": 7}
{"curie": "MONDO:0009433", "names": ["HLHS", "HLHS1", "hypoplastic left heart syndrome 1", "HYPOPLASTIC LEFT HEART SYNDROME 1", "GJA1 hypoplastic left heart syndrome", "hypoplastic left heart syndrome type 1", "hypoplastic left heart syndrome caused by mutation in GJA1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypoplastic left heart syndrome 1", "shortest_name_length": 4}
{"curie": "MONDO:0013865", "names": ["COXPD10", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 10", "combined oxidative phosphorylation deficiency 10", "combined oxidative phosphorylation defect type 10", "Combined oxidative phosphorylation defect type 10", "MTO1 combined oxidative phosphorylation deficiency", "combined oxidative phosphorylation deficiency type 10", "COXPD10 - combined oxidative phosphorylation defect type 10", "infantile hypertrophic mitochondrial cardiomyopathy and lactic acidosis", "combined oxidative phosphorylation deficiency caused by mutation in MTO1", "CARDIOMYOPATHY, INFANTILE HYPERTROPHIC MITOCHONDRIAL, AND LACTIC ACIDOSIS", "cardiomyopathy, infantile hypertrophic mitochondrial, and lactic acidosis", "mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency", "Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency", "Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to mitochondrial transfer ribonucleic acid translation optimisation 1 deficiency", "Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to mitochondrial transfer ribonucleic acid translation optimization 1 deficiency", "Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to mitochondrial transfer ribonucleic acid translation optimization 1 deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency", "shortest_name_length": 7}
{"curie": "UMLS:C2828200", "names": ["Stage IB Bone Cancer", "Stage IB Bone Cancer AJCC v7", "Stage IB Bone Cancer  AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Bone Cancer AJCC v7", "shortest_name_length": 20}
{"curie": "MONDO:0018203", "names": ["LCPS", "LMNA-related cardiocutaneous progeria syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "LMNA-related cardiocutaneous progeria syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0016568", "names": ["Lowe Kohn Cohen syndrome", "Lowe-Kohn-Cohen syndrome", "deafness nephritis anorectal malformation", "Deafness nephritis ano rectal malformation", "deafness - nephritis - ano-rectal malformation", "Deafness-nephritis-ano-rectal malformation syndrome", "deafness-nephritis-ano-rectal malformation syndrome", "Deafness, nephritis, anorectal malformation syndrome", "Hearing loss-nephritis-ano-rectal malformation syndrome", "Dominant ano-rectal malformation, nephritis and nerve-deafness", "dominant ano-rectal malformation, nephritis and nerve-deafness", "Deafness, nephritis, anorectal malformation syndrome (disorder)", "Deafness, nephritis, anorectal malformation syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lowe-Kohn-Cohen syndrome", "shortest_name_length": 24}
{"curie": "MONDO:0054754", "names": ["IIAE8", "Herpes simplex encephalitis, Susceptibility to, 6", "HERPES SIMPLEX ENCEPHALITIS, SUSCEPTIBILITY TO, 6", "ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 8", "encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 8", "encephalopathy, ACUTE, infection-induced (HERPES-specific), susceptibility to, 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 8", "shortest_name_length": 5}
{"curie": "UMLS:C4527065", "names": ["Merkel Cell Carcinoma by AJCC v8 Pathologic Stage", "Neuroendocrine Carcinoma of the Skin by AJCC v8 Pathologic Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Merkel Cell Carcinoma by AJCC v8 Pathologic Stage", "shortest_name_length": 49}
{"curie": "UMLS:C1518188", "names": ["Malignant Lymphoma Follicular, Large Noncleaved Cell Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Lymphoma Follicular, Large Noncleaved Cell Type", "shortest_name_length": 57}
{"curie": "UMLS:C0596793", "names": ["hematoma intracranial", "Intracranial hematoma", "intracranial hematoma", "intracranial haematoma", "Intracranial haematoma", "hematomas intracranial", "Intracranial hematoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intracranial hematoma", "shortest_name_length": 21}
{"curie": "MONDO:0060764", "names": ["TETAMS1", "tetraamelia syndrome 1", "TETRAAMELIA SYNDROME 1", "tetra-amelia syndrome 1", "Tetra-amelia syndrome 1", "tetraamelia syndrome, autosomal recessive", "TETRAAMELIA SYNDROME, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tetraamelia syndrome 1", "shortest_name_length": 7}
{"curie": "MONDO:0006602", "names": ["porokeratosis", "Porokeratosis", "Porokeratosis, NOS", "porokeratosis (disease)", "Porokeratosis (disorder)", "porokeratosis (diagnosis)", "disseminated superficial actinic porokeratosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "porokeratosis", "shortest_name_length": 13}
{"curie": "MONDO:0030690", "names": ["PFBMFT6", "PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 6", "pulmonary fibrosis and/or bone marrow failure, telomere-related, 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary fibrosis and/or bone marrow failure, telomere-related, 6", "shortest_name_length": 7}
{"curie": "MONDO:0012767", "names": ["ARMD11", "age related macular degeneration 11", "Macular Degeneration, Age-Related, 11", "macular degeneration, age-related, 11", "CST3 age-related macular degeneration", "MACULAR DEGENERATION, AGE-RELATED, 11", "age related macular degeneration type 11", "Age-Related Macular Degeneration type 11", "macular Degeneration, age-related, type 11", "age-related macular degeneration caused by mutation in CST3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "age related macular degeneration 11", "shortest_name_length": 6}
{"curie": "MONDO:0013242", "names": ["MODY11", "maturity-onset diabetes of the young type 11", "maturity-onset diabetes of the young, type 11", "Maturity-onset diabetes of the young, type 11", "MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 11", "maturity-onset diabetes of the young - type 11", "BLK maturity-onset diabetes of the young (disease)", "Maturity-onset diabetes of the young, type 11 (disorder)", "maturity-onset diabetes of the young - type 11 (diagnosis)", "maturity-onset diabetes of the young (disease) caused by mutation in BLK"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maturity-onset diabetes of the young type 11", "shortest_name_length": 6}
{"curie": "UMLS:C5238476", "names": ["Adnexal Adenocarcinoma, NOS", "Adnexal Adenocarcinoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adnexal Adenocarcinoma, Not Otherwise Specified", "shortest_name_length": 27}
{"curie": "MONDO:0005719", "names": ["coronavirus", "Coronavirus", "Coronavirus Infection", "Coronavirus infection", "coronavirus infection", "Corona virus infection", "Coronavirus infections", "Coronavirus Infections", "Infection, Coronavirus", "corona infection virus", "corona infections virus", "Infections, Coronavirus", "infection; viral, coronavirus", "coronavirus infectious disease", "Coronavinae infectious disease", "Coronavirus infection (disorder)", "Coronavirus infection (diagnosis)", "Coronavirus infection, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Coronavinae infectious disease", "shortest_name_length": 11}
{"curie": "MONDO:0012800", "names": ["MFT2", "Mft2", "trichoepithelioma multiple familial 2", "multiple familial trichoepithelioma 2", "trichoepithelioma, multiple familial, 2", "TRICHOEPITHELIOMA, MULTIPLE FAMILIAL, 2", "Trichoepithelioma, Multiple Familial, 2", "trichoepithelioma, multiple familial, type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichoepithelioma, multiple familial, 2", "shortest_name_length": 4}
{"curie": "MONDO:0018045", "names": ["HHS", "Hoyeraal-Hreidarsson syndrome", "HOYERAAL-HREIDARSSON SYNDROME", "Hoyeraal-Hreidarsson Syndrome", "Hoyeraal Hreidarsson syndrome", "Cerebellar hypoplasia with pancytopenia", "CEREBELLAR HYPOPLASIA WITH PANCYTOPENIA", "Hoyeraal-Hreidarsson syndrome (disorder)", "Progressive pancytopenia-immunodeficiency-cerebellar hypoplasia syndrome", "progressive pancytopenia-immunodeficiency-cerebellar hypoplasia syndrome", "Growth retardation prenatal with progressive pancytopenia and cerebellar hypoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hoyeraal-Hreidarsson syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0018653", "names": ["PPAP", "Polymerase Proofreading Associated Polyposis", "Polymerase proofreading-related adenomatous polyposis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Polymerase proofreading-related adenomatous polyposis", "shortest_name_length": 4}
{"curie": "MONDO:0008845", "names": ["Atonic-Astatic Syndrome of Foerster", "ATONIC-ASTATIC SYNDROME OF FOERSTER", "atonic-astatic syndrome of Foerster"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atonic-astatic syndrome of Foerster", "shortest_name_length": 35}
{"curie": "UMLS:C4526897", "names": ["Soft Tissue Sarcoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Soft Tissue Sarcoma by AJCC v8 Stage", "shortest_name_length": 36}
{"curie": "UMLS:C1262206", "names": ["IT Band Syndrome", "Iliotibial band syndrome", "Iliotibial Band Syndrome", "syndrome; iliotibial band", "iliotibial band; syndrome", "iliotibial band friction syndrome", "Iliotibial band friction syndrome", "Iliotibial band friction syndrome (disorder)", "iliotibial band friction syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Iliotibial Band Syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0016826", "names": ["MAHCC", "CblC defect", "Cobalamin C defect", "cobalamin C disease", "Cobalamin C disease", "CblC - Cobalamin locus C", "Cobalamin locus C variant", "Cobalamin C disease (disorder)", "cobalamin C disease (diagnosis)", "Methylmalonic acidemia and homocystinemia", "methylmalonic acidemia and homocystinemia", "methylmalonic aciduria and homocystinuria", "Methylmalonic acidemia with homocystinuria", "methylmalonic aciduria with homocystinuria", "Methylmalonic aciduria with homocystinuria", "CblC methylmalonic acidemia and homocystinuria", "CblC methylmalonic acidaemia and homocystinuria", "Methylmalonic acidemia and homocystinuria cblC type", "METHYLMALONIC ACIDEMIA AND HOMOCYSTINURIA, cblC TYPE", "METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE", "Methylmalonic Acidemia and Homocystinuria, CblC Type", "Methylmalonic Aciduria and Homocystinuria, cblC Type", "Methylmalonic Aciduria and Homocystinuria, CblC Type", "Methylmalonic acidemia with homocystinuria, type cblC", "Methylmalonic aciduria with homocystinuria, type cblC", "Cobalamin-C methylmalonic acidemia and homocystinuria", "METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, VITAMIN B12-RESPONSIVE", "Methylmalonic Aciduria and Homocystinuria, Vitamin B12-Responsive", "Combined defect in adenosylcobalamin and methylcobalamin synthesis", "combined defect in adenosylcobalamin and methylcobalamin synthesis", "Combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblC", "VITAMIN B12 METABOLIC DEFECT WITH COMBINED DEFICIENCY OF METHYLMALONYL-CoA MUTASE AND HOMOCYSTEINE:METHYLTETRAHYDROFOLATE METHYLTRANSFERASE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "methylmalonic aciduria and homocystinuria", "shortest_name_length": 5}
{"curie": "UMLS:C1335008", "names": ["Non-Neoplastic External Ear Disease", "Non-Neoplastic External Ear Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic External Ear Disorder", "shortest_name_length": 35}
{"curie": "MONDO:0031003", "names": ["FHCA2", "NTCP Deficiency", "NTCP DEFICIENCY", "hypercholanemia, familial 2", "hypercholanemia, familial, 2", "HYPERCHOLANEMIA, FAMILIAL, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypercholanemia, familial, 2", "shortest_name_length": 5}
{"curie": "MONDO:0011074", "names": ["DFNA7", "autosomal dominant deafness 7", "deafness, autosomal dominant 7", "DEAFNESS, AUTOSOMAL DOMINANT 7", "Deafness, Autosomal Dominant 7", "DEAFNESS, AUTOSOMAL DOMINANT 7 (disorder)", "autosomal dominant nonsyndromic deafness 7", "autosomal dominant nonsyndromic hearing loss 7", "autosomal dominant nonsyndromic deafness type 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 7", "shortest_name_length": 5}
{"curie": "MONDO:0019632", "names": ["Borrelia", "lyme disease", "Lyme Disease", "Disease;lyme", "Lyme disease", "LYME DISEASE", "disease; Lyme", "Lyme; disease", "lymes disease", "Disease, Lyme", "Lyme's disease", "lyme's disease", "Lyme borreliosis", "Steere's disease", "lyme borreliosis", "Lyme Borreliosis", "neuroborreliosis", "Borreliosis, Lyme", "bannwarth syndrome", "Bannwarth syndrome", "bannworth's syndrome", "Bannworth's syndrome", "lyme neuroborreliosis", "Lyme Neuroborreliosis", "Lyme neuroborreliosis", "Neuroborreliosis, Lyme", "LYME DISEASE, EARLY/MID", "Lyme disease (disorder)", "lyme disease (diagnosis)", "B. burgdorferi Infection", "Lyme disease, unspecified", "neurological Lyme disease", "neurological lyme disease", "Neurological Lyme disease", "B. burgdorferi Infections", "Nervous System Lyme Disease", "Lyme Disease, Nervous System", "Bannwarth syndrome (disorder)", "Tick-borne meningopolyneuritis", "Borrelia burgdorferi infection", "Borrelia Burgdorferi Infection", "borrelia burgdorferi infection", "Bannwarth syndrome (diagnosis)", "Borrelia burgdorferi Infection", "Nervous System Lyme Borreliosis", "Borrelia burgdorferi Infections", "Lyme Borreliosis, Nervous System", "Garin-Bujadoux-Bannwarth syndrome", "Infection by Borrelia burgdorferi", "Borrelia burgdorferi Neuroborreliosis", "disease (or disorder); Lyme (disease)", "Neuroborrelioses, Borrelia burgdorferi", "Neuroborreliosis, Borrelia burgdorferi", "neurological disorders in lyme disease", "Borreliella burgdorferi infectious disease", "Borreliella burgdorferi disease or disorder", "Infection due to Borrelia burgdorferi sensu lato", "Borreliella burgdorferi caused disease or disorder", "neurological disorders in lyme disease (diagnosis)", "Lyme disease infection of CNS caused by Borrelia burgdorferi", "Infection of central nervous system caused by Borrelia burgdorferi", "Infection of central nervous system caused by Borrelia burgdorferi (disorder)", "Infection of central nervous system caused by Borrelia burgdorferi (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lyme disease", "shortest_name_length": 8}
{"curie": "UMLS:C1336416", "names": ["Stage IV Extragonadal Seminoma", "stage IV extragonadal seminoma", "Stage IV Extragonadal Primary Seminoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Extragonadal Seminoma", "shortest_name_length": 30}
{"curie": "MONDO:0033652", "names": ["MC4DN17", "mitochondrial complex 4 deficiency, nuclear type 17", "mitochondrial complex IV deficiency, nuclear type 17", "MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 17"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 4 deficiency, nuclear type 17", "shortest_name_length": 7}
{"curie": "UMLS:C2213017", "names": ["Meningeal Lymphoma", "meningeal lymphoma", "lymphomatous meningitis", "Lymphomatous Meningitis", "Leptomeningeal Lymphoma", "meningitis, lymphomatous", "lymphomatous leptomeningitis", "leptomeningitis, lymphomatous", "malignant lymphoma of meninges", "malignant lymphoma of meninges (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meningeal Lymphoma", "shortest_name_length": 18}
{"curie": "UMLS:C1514513", "names": ["Prostate Ductal Adenocarcinoma, Solid Pattern"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Ductal Adenocarcinoma, Solid Pattern", "shortest_name_length": 45}
{"curie": "MONDO:0017772", "names": ["oral erosive lichen"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oral erosive lichen", "shortest_name_length": 19}
{"curie": "MONDO:0009469", "names": ["BRIC1", "BRIC type 1", "Bric type 1", "Summerskill syndrome", "SUMMERSKILL SYNDROME", "mild ATP8B1 deficiency", "cholestasis, benign recurrent intrahepatic", "benign recurrent intrahepatic cholestasis 1", "Cholestasis, benign recurrent intrahepatic 1", "cholestasis, benign recurrent intrahepatic 1", "cholestasis, benign recurrent intrahepatic, 1", "Cholestasis, Benign Recurrent Intrahepatic, 1", "recurrent familial intrahepatic cholestasis 1", "CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC, 1", "benign recurrent intrahepatic cholestasis type 1", "ATP8B1 benign recurrent intrahepatic cholestasis", "Benign recurrent intrahepatic cholestasis type 1", "cholestasis, benign recurrent intrahepatic, type 1", "benign recurrent intrahepatic cholestasis caused by mutation in ATP8B1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign recurrent intrahepatic cholestasis type 1", "shortest_name_length": 5}
{"curie": "MONDO:0008115", "names": ["FS", "MMT", "FS1", "ODED", "MODED", "FGLDS", "FGLDS1", "MMT type 1", "MMT SYNDROME", "MMT Syndrome", "Mmt syndrome", "Oded syndrome", "ODED syndrome", "ODED Syndrome", "ODED SYNDROME", "MODED syndrome", "Feingold syndrome", "Feingold Syndrome", "FEINGOLD SYNDROME", "Feingold syndrome 1", "FEINGOLD SYNDROME 1", "ODED syndrome type 1", "MODED syndrome type 1", "MYCN Feingold syndrome", "Brunner Winter syndrome", "Brunner-Winter syndrome", "Feingold syndrome type 1", "Brunner-Winter syndrome type 1", "Oculodigitoesophagoduodenal syndrome", "oculodigitoesophagoduodenal syndrome", "OCULODIGITOESOPHAGODUODENAL SYNDROME", "Oculo-digito-esophagoduodenal syndrome", "oculo-digito-esophagoduodental syndrome", "Oculo-digito-oesophagoduodenal syndrome", "Oculo-digito-esophageal-duodenal syndrome", "Oculo-digito-oesophageal-duodenal syndrome", "Feingold syndrome caused by mutation in MYCN", "Oculo-Digito-Esophagoduodental (ODED) Syndrome", "oculo-digito-esophagoduodental (ODED) syndrome", "oculo-digito-esophageal-duodenal syndrome type 1", "Oculo-digito-esophageal-duodenal syndrome type 1", "Microcephaly-oculo-digito-esophageal-duodenal syndrome", "MICROCEPHALY-OCULO-DIGITO-ESOPHAGEAL-DUODENAL SYNDROME", "microcephaly-oculo-digito-esophageal-duodenal syndrome", "Microcephaly-oculo-digito-oesophageal-duodenal syndrome", "Microcephaly-digital anomalies-normal intelligence syndrome", "microcephaly-oculo-digito-esophageal-duodenal (MODED) syndrome", "Microcephaly-Oculo-Digito-Esophageal-Duodenal (MODED) Syndrome", "Microcephaly and Digital Abnormalities with Normal Intelligence", "microcephaly and digital abnormalities with normal intelligence", "Microcephaly-oculo-digito-esophageal-duodenal syndrome syndrome", "MICROCEPHALY AND DIGITAL ABNORMALITIES WITH NORMAL INTELLIGENCE", "Microcephaly-oculo-digito-esophageal-duodenal syndrome (disorder)", "Microcephaly-mesobrachyphalangy-tracheoesophageal fistula syndrome", "microcephaly-digital anomalies-normal intelligence syndrome type 1", "microcephaly-mesobrachyphalangy-tracheoesophageal fistula syndrome", "Microcephaly-digital anomalies-normal intelligence syndrome type 1", "MODED syndrome Microcephaly-Oculo-Digito-Esophageal-Duodenal Syndrome", "Microcephaly-oculo-digito-esophageal-duodenal syndrome syndrome type 1", "microcephaly-oculo-digito-esophageal-duodenal syndrome syndrome type 1", "Microcephaly-intellectual disability-tracheoesophageal fistula syndrome", "MICROCEPHALY, MENTAL RETARDATION, AND TRACHEOESOPHAGEAL FISTULA SYNDROME", "microcephaly-mesobrachyphalangy-tracheoesophageal fistula (MMT) syndrome", "microcephaly, mental retardation, and tracheoesophageal fistula syndrome", "Microcephaly-Mesobrachyphalangy-Tracheoesophageal Fistula (MMT) Syndrome", "Microcephaly, Mental Retardation, and Tracheoesophageal Fistula Syndrome", "microcephaly, intellectual disability, and tracheoesophageal fistula syndrome", "Microcephaly-intellectual disability-tracheoesophageal fistula syndrome type 1", "microcephaly-intellectual disability-tracheoesophageal fistula syndrome type 1", "tracheoesophageal fistula-esophageal atresia-multiple congenital anomaly syndrome", "Digital Anomalies with Short Palpebral Fissures and Atresia of Esophagus or Duodenum", "digital anomalies-short palpebral fissures-atresia of esophagus or duodenum syndrome", "Digital anomalies with short palpebral fissures and atresia of esophagus or duodenum", "DIGITAL ANOMALIES WITH SHORT PALPEBRAL FISSURES AND ATRESIA OF ESOPHAGUS OR DUODENUM", "digital anomalies with short palpebral fissures and atresia of esophagus or duodenum", "digital anomalies with short palpebral fissures and atresia of esophagus or duodenum type 1", "Digital anomalies with short palpebral fissures and atresia of esophagus or duodenum type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Feingold syndrome type 1", "shortest_name_length": 2}
{"curie": "UMLS:C1504377", "names": ["Hyperglycemic hyperosmolar nonketotic syndrome", "Hyperglycaemic hyperosmolar nonketotic syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyperglycemic hyperosmolar nonketotic syndrome", "shortest_name_length": 46}
{"curie": "MONDO:0013450", "names": ["CSNB1D", "Csnb, complete, autosomal recessive", "CSNB, COMPLETE, AUTOSOMAL RECESSIVE", "congenital stationary night blindness 1D", "congenital stationary night blindness type 1D", "SLC24A1 congenital stationary night blindness", "congenital stationary night blindness - type 1d", "NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1D", "night blindness, congenital stationary, type 1D", "congenital stationary night blindness - type 1d (diagnosis)", "congenital stationary night blindness 1D autosomal recessive", "congenital stationary night blindness caused by mutation in SLC24A1", "night blindness, congenital stationary (complete), 1D, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital stationary night blindness 1D", "shortest_name_length": 6}
{"curie": "UMLS:C1378462", "names": ["stage IV oropharynx cancer", "stage IV oropharyngeal cancer", "oropharynx cancer, metastatic", "Stage IV Oropharynx Carcinoma", "Oropharyngeal Cancer Stage IV", "oropharyngeal cancer, stage IV", "metastatic oropharyngeal cancer", "oropharyngeal cancer, metastatic", "Stage IV Carcinoma of Oropharynx", "Stage IV Oropharyngeal Carcinoma", "Stage IV Oropharyngeal Throat Cancer", "Stage IV Carcinoma of the Oropharynx", "Oropharyngeal Cancer Stage IV AJCC v6", "Stage IV Oropharynx Carcinoma AJCC v6", "Stage IV Oropharyngeal Cancer AJCC v6", "Stage IV Carcinoma of Oropharynx AJCC v6", "Stage IV Oropharyngeal Carcinoma AJCC v6", "Stage IV Carcinoma of the Oropharynx AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Oropharyngeal Carcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0007058", "names": ["ACRPV", "F SYNDROME", "F syndrome", "ACROPECTOROVERTEBRAL DYSPLASIA", "Acropectorovertebral dysplasia", "acropectorovertebral dysplasia", "acropectorovertebral dysplasia F form", "Acropectorovertebral Dysplasia, F-Form", "Acropectorovertebral dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acropectorovertebral dysplasia", "shortest_name_length": 5}
{"curie": "UMLS:C0221745", "names": ["SUICIDAL DEPRESSION", "Suicidal depression", "Depression suicidal", "DEPRESSION SUICIDAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Depression suicidal", "shortest_name_length": 19}
{"curie": "MONDO:0002187", "names": ["vulva disease", "disease vulva", "VULVA DISORDER", "Vulva disorder", "diseases vulva", "Vulvar Disease", "vulvar disease", "Disorder vulva", "DISORDER VULVA", "Disorder;vulva", "Vulva--Diseases", "disorders vulva", "Vulvar Disorder", "vulvar diseases", "Disease, Vulvar", "Vulvar disorder", "Vulval disorder", "Vulvar Diseases", "vulvar disorder", "vulval disorder", "disorders vulval", "disorders vulvar", "Diseases, Vulvar", "Vulvar Disorders", "disease of vulva", "Disorder of vulva", "disorder of vulva", "Vulva disorder NOS", "Vulval disorder NOS", "Vulvar disorder, NOS", "Vulval disorder, NOS", "disorder of the vulva", "Disease of vulva, NOS", "disease (or disorder); vulva", "Disorder of vulva (disorder)", "disorder of vulva (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar disease", "shortest_name_length": 13}
{"curie": "MONDO:0010620", "names": ["Hypouricemia, Familial Renal, due to Tubular Hypersecretion", "HYPOURICEMIA, FAMILIAL RENAL, DUE TO TUBULAR HYPERSECRETION", "hypouricemia, familial renal, due to tubular hypersecretion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypouricemia, familial renal, due to tubular hypersecretion", "shortest_name_length": 59}
{"curie": "UMLS:C1112565", "names": ["Pneumatosis intestinalis", "pneumatosis intestinalis", "Pneumatosis Intestinalis", "pneumatosis; intestinalis", "intestinalis; pneumatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pneumatosis intestinalis", "shortest_name_length": 24}
{"curie": "UMLS:C1701474", "names": ["Quarrelsomeness", "quarrelsomeness", "Argumentativeness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Argumentativeness", "shortest_name_length": 15}
{"curie": "UMLS:C0237010", "names": ["simple ovarian cyst", "Simple Ovarian Cyst", "Ovarian simple cyst", "OVARIAN CYST SIMPLE", "ovarian cyst simple", "ovarian simple cyst", "Simple cyst of ovary", "Simple Cyst of Ovary", "cysts ovarian simple", "Simple Cyst of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Simple Ovarian Cyst", "shortest_name_length": 19}
{"curie": "UMLS:C0206677", "names": ["Polypoid adenoma", "polypoid adenoma", "Polypoid Adenoma", "Adenomatous Polyp", "POLYP ADENOMATOUS", "adenomatous polyp", "Adenomatous polyp", "Polyp, Adenomatous", "Adenomatous Polyps", "Adenomatous polyps", "adenomatous polyps", "Polyps, Adenomatous", "Adenomatous polyp NOS", "Adenomatous polyp, NOS", "GI Tract Adenomatous Polyp", "Gastrointestinal Tract Adenomatous Polyp", "Adenomatous polyp (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenomatous Polyps", "shortest_name_length": 16}
{"curie": "MONDO:0013839", "names": ["HSAN6", "HSAN 6", "HSAN VI", "familial dysautonomia with contractures", "Familial dysautonomia with contractures", "DST hereditary sensory and autonomic neuropathy", "hereditary sensory and autonomic neuropathy type 6", "Hereditary sensory and autonomic neuropathy type 6", "hereditary sensory and autonomic neuropathy type VI", "Hereditary sensory and autonomic neuropathy type VI", "neuropathy, hereditary sensory and autonomic, type 6", "neuropathy, hereditary sensory and autonomic, type VI", "NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI", "hereditary sensory and autonomic neuropathy caused by mutation in DST"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary sensory and autonomic neuropathy type 6", "shortest_name_length": 5}
{"curie": "MONDO:0045032", "names": ["Congenital secretory diarrhea", "congenital secretory diarrhea", "Congenital secretory diarrhoea", "Congenital secretory diarrhea, NOS", "Congenital secretory diarrhoea, NOS", "Congenital secretory diarrhea (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital secretory diarrhea", "shortest_name_length": 29}
{"curie": "UMLS:C0679360", "names": ["Foodborne Disease", "Foodborne Illness", "Food-borne Illness", "Foodborne diseases", "Food borne Illness", "Food borne Disease", "food borne disease", "Illness, Foodborne", "Foodborne Diseases", "Food-borne Disease", "Disease, Foodborne", "food borne disorder", "Illness, Food-borne", "Food-borne Diseases", "Food borne Diseases", "borne diseases food", "Disease, Food-borne", "Foodborne Illnesses", "Illnesses, Foodborne", "Food borne Illnesses", "Food-borne Illnesses"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Foodborne Disease", "shortest_name_length": 17}
{"curie": "MONDO:0018898", "names": ["Skin Lymphoma", "cutaneous lymphoma", "primary skin lymphoma", "Primary Skin Lymphoma", "Cutaneous (Skin) Lymphoma", "cutaneous (skin) lymphoma", "primary cutaneous lymphoma", "Primary cutaneous lymphoma", "Primary Cutaneous Lymphoma", "Skin cancer, cutaneous lymphoma", "Primary cutaneous lymphoma (disorder)", "Primary cutaneous lymphoma (diagnosis)", "skin malignant lymphoma primary cutaneous", "Primary cutaneous lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary cutaneous lymphoma", "shortest_name_length": 13}
{"curie": "MONDO:0022946", "names": ["deafness progressive cataract autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness progressive cataract autosomal dominant", "shortest_name_length": 48}
{"curie": "MONDO:0002031", "names": ["cecal disease", "Cecal Disease", "cecal disorder", "cecum; disease", "Cecal Diseases", "Disease, Cecal", "caecum disease", "Diseases, Cecal", "disease of caecum", "Disorder of cecum", "disorder of cecum", "disorder of caecum", "Disorder of caecum", "caecum disease or disorder", "disease (or disorder); cecum", "Disorder of cecum (disorder)", "disease or disorder of caecum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cecal disorder", "shortest_name_length": 13}
{"curie": "UMLS:C3273138", "names": ["Extrahepatic Bile Duct Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extrahepatic Bile Duct Neuroendocrine Neoplasm", "shortest_name_length": 46}
{"curie": "MONDO:0010099", "names": ["AB variant", "GM2 Activator Deficiency", "GM2 ACTIVATOR DEFICIENCY", "GM2 activator deficiency", "Deficiency, GM2 Activator", "Activator Deficiency, GM2", "GM2 Activator Deficiencies", "Activator Deficiencies, GM2", "GM2 gangliosidosis, type AB", "Gangliosidosis GM2, Type AB", "GM2 Gangliosidosis, Type AB", "Deficiencies, GM2 Activator", "Tay-Sachs disease AB variant", "AB Variant GM2-Gangliosidosis", "Tay-Sachs Disease, AB Variant", "AB Variant GM2-Gangliosidoses", "AB VARIANT GM2-GANGLIOSIDOSIS", "Tay-Sachs disease, AB variant", "Ab variant GM2-gangliosidosis", "Tay-Sachs disease, variant AB", "Tay Sachs Disease, AB Variant", "AB Variant Gangliosidosis GM2", "GM>2< gangliosidosis, type AB", "AB Variant GM2 Gangliosidosis", "TAY-SACHS DISEASE, AB VARIANT", "GM2-GANGLIOSIDOSIS, AB VARIANT", "GM2 gangliosidosis, AB variant", "GM2 Gangliosidosis, AB Variant", "Gangliosidosis GM2, AB Variant", "GM2-Gangliosidoses, AB Variant", "Variant GM2-Gangliosidosis, AB", "Variant GM2-Gangliosidoses, AB", "GM2-gangliosidosis, AB variant", "GM2-Gangliosidosis, AB Variant", "GM2 Activator Deficiency Disease", "Hexosaminidase activator deficiency", "Hexosaminidase Activator Deficiency", "hexosaminidase activator deficiency", "HEXOSAMINIDASE ACTIVATOR DEFICIENCY", "Deficiency, Hexosaminidase Activator", "Activator Deficiency, Hexosaminidase", "Hexosaminidase Activator Deficiencies", "Activator Deficient Tay Sachs Disease", "Activator-Deficient Tay-Sachs Disease", "Deficiencies, Hexosaminidase Activator", "Disease, Activator-Deficient Tay-Sachs", "Activator-Deficient Tay-Sachs Diseases", "Tay-Sachs Disease, Activator-Deficient", "GM<sub>2</sub> gangliosidosis, type AB", "Activator Deficiencies, Hexosaminidase", "Tay-Sachs Diseases, Activator-Deficient", "Activator Deficiency GM2 Gangliosidosis", "Diseases, Activator-Deficient Tay-Sachs", "GM2 Protein Activator Deficiency Disease", "Tay-Sachs disease, variant AB (disorder)", "Deficiency Disease, GM2 Protein Activator", "Hexosaminidase Activator Protein Deficiency Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tay-Sachs disease AB variant", "shortest_name_length": 10}
{"curie": "UMLS:C1709469", "names": ["Accessory Urethral Gland Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Accessory Urethral Gland Neoplasm", "shortest_name_length": 33}
{"curie": "MONDO:0001439", "names": ["episcleritis periodica fugax", "Episcleritis periodica fugax", "periodica fugax; episcleritis", "episcleritis; periodica fugax", "Episcleritis periodica fugax (disorder)", "episcleritis periodica fugax (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "episcleritis periodica fugax", "shortest_name_length": 28}
{"curie": "MONDO:0054665", "names": ["PITA3", "pituitary adenoma 3", "PITUITARY ADENOMA 3, MULTIPLE TYPES", "pituitary adenoma 3, multiple types", "pituitary adenoma 3, multiple types, somatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pituitary adenoma 3, multiple types", "shortest_name_length": 5}
{"curie": "UMLS:C3887662", "names": ["Spinal Tumors", "neoplasm spinal", "Spinal Neoplasms", "spinal neoplasms", "Intraspinal Tumor", "Spinal Canal Tumors", "Intraspinal Neoplasm", "Intraspinal Neoplasms", "Spinal Canal and Spinal Cord Tumor", "Spinal Canal and Spinal Cord Neoplasm", "Tumor of Spinal Canal and Spinal Cord", "Neoplasm of Spinal Canal and Spinal Cord", "Tumor of the Spinal Canal and Spinal Cord", "Neoplasms of Spinal Canal and Spinal Cord", "Neoplasm of the Spinal Canal and Spinal Cord", "Neoplasms of the Spinal Canal and Spinal Cord"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraspinal Neoplasm", "shortest_name_length": 13}
{"curie": "MONDO:0032817", "names": ["NDCAGF", "neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies", "NEURODEVELOPMENTAL DISORDER WITH CATARACTS, POOR GROWTH, AND DYSMORPHIC FACIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies", "shortest_name_length": 6}
{"curie": "MONDO:0019193", "names": ["Lawrence syndrome", "Lawrence-Seip syndrome", "Acquired total lipoatrophy", "acquired lipoatrophic diabetes", "Acquired lipoatrophic diabetes", "Acquired lipodystrophic diabetes", "acquired generalized lipodystrophy", "Acquired generalized lipodystrophy", "Acquired Generalized Lipodystrophy", "Acquired generalised lipodystrophy", "Acquired generalized lipodystrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired generalized lipodystrophy", "shortest_name_length": 17}
{"curie": "MONDO:0003425", "names": ["ophthalmoplegia", "Ophthalmoplegia", "oculomotor paralysis", "Total ophthalmoplegia", "total ophthalmoplegia", "total; ophthalmoplegia", "eye movement paralysis", "ophthalmoplegia; total", "Global paralysis of gaze", "Complete ophthalmoplegia", "extraocular muscle paralysis", "Total ophthalmoplegia (disorder)", "total ophthalmoplegia (diagnosis)", "Total internal and external ophthalmoplegia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ophthalmoplegia", "shortest_name_length": 15}
{"curie": "MONDO:0002831", "names": ["Ringertz carcinoma", "Ringertz Carcinoma", "Schneiderian carcinoma", "Schneiderian Carcinoma", "cylindrical cell carcinoma", "Cylindrical cell carcinoma", "Sinonasal Schneiderian carcinoma", "Sinonasal Schneiderian Carcinoma", "sinonasal squamous cell carcinoma", "Schneiderian carcinoma (diagnosis)", "Sinonasal cylindrical cell carcinoma", "Sinonasal Cylindrical Cell Carcinoma", "Sinonasal transitional cell carcinoma", "Sinonasal Transitional Cell Carcinoma", "malignant neoplasm carcinoma Schneiderian", "Schneiderian carcinoma (morphologic abnormality)", "Non-Keratinizing Sinonasal Squamous Cell Carcinoma", "non-keratinizing sinonasal squamous cell carcinoma", "Sinonasal Non-Keratinizing Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-keratinizing sinonasal squamous cell carcinoma", "shortest_name_length": 18}
{"curie": "UMLS:C1838951", "names": ["Atpase Deficiency, Nuclear-Encoded", "Leigh Syndrome Due To Mitochondrial Complex I Deficiency", "LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY", "shortest_name_length": 34}
{"curie": "MONDO:0021447", "names": ["benign tumor of testis", "Benign tumor of testis", "testis benign neoplasm", "Benign Tumor of Testis", "Benign tumour of testis", "Benign testicular tumor", "Benign Testicular Tumor", "benign testicular tumor", "Benign testicular tumour", "benign neoplasm of testis", "Benign Neoplasm of Testis", "Benign neoplasm of testis", "Benign Tumor of the Testis", "Benign Testicular Neoplasm", "benign tumor of the testis", "benign testicular neoplasm", "benign neoplasm of the testis", "Benign Neoplasm of the Testis", "Benign testicular neoplasm NOS", "Benign neoplasm of testis, NOS", "Benign neoplasm of testis (disorder)", "benign neoplasm of testis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of testis", "shortest_name_length": 22}
{"curie": "MONDO:0100164", "names": ["PDMI", "PNDM", "monogenic diabetes of infancy", "Permanent neonatal diabetes mellitus", "neonatal diabetes mellitus permanent", "Permanent Neonatal Diabetes Mellitus", "permanent neonatal diabetes mellitus", "Diabetes Mellitus, Permanent Neonatal", "DIABETES MELLITUS, PERMANENT NEONATAL", "diabetes mellitus, permanent neonatal", "permanent diabetes mellitus of infancy", "Permanent diabetes mellitus of infancy", "diabetes mellitus, permanent, of infancy", "Diabetes Mellitus, Permanent, of Infancy", "Permanent neonatal diabetes mellitus (disorder)", "Permanent neonatal diabetes mellitus (diagnosis)", "developmental delay, epilepsy, and neonatal diabetes", "diabetes mellitus, permanent neonatal, with neurologic features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "permanent neonatal diabetes mellitus", "shortest_name_length": 4}
{"curie": "UMLS:C5239059", "names": ["Advanced Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Liposarcoma", "shortest_name_length": 20}
{"curie": "UMLS:C4727773", "names": ["Refractory Non-Small Cell Lung Cancer", "Refractory Non-Small Cell Lung Carcinoma", "Refractory Lung Non-Small Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Lung Non-Small Cell Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0003569", "names": ["cranial neuropathy", "Cranial neuropathy", "Cranial Neuropathy", "Neuropathy, Cranial", "Cranial Neuropathies", "cranial neuropathies", "Cranial Nerve Disease", "Neuropathies, Cranial", "cranial nerve disease", "cranial disease nerve", "Cranial Nerve Diseases", "Cranial neuropathy NOS", "Cranial nerve diseases", "Cranial Nerve Disorder", "Cranial nerve disorder", "cranial nerve disorder", "cranial nerve diseases", "cranial nerve disorders", "Cranial Nerve Disorders", "CRANIAL NERVE DISORDERS", "cranial disorders nerves", "cranial nerve neuropathy", "Disorder of Cranial Nerve", "Disorder of cranial nerve", "Nervus Cranialis Disorder", "disorder of cranial nerve", "Nervus Cranialis Disorders", "Cranial nerve disorder NOS", "Cranial nerve disorder, NOS", "Cranial nerve disease or syndrome", "Cranial nerve disorder (disorder)", "Cranial nerve disorder, unspecified", "Cranial Nerve Diseases and Syndromes", "disease (or disorder); cranial nerve", "disorder of cranial nerve (diagnosis)", "Unspecified disorder of cranial nerves", "cranial neuron projection bundle disease", "disease of cranial neuron projection bundle", "disorder of cranial neuron projection bundle", "cranial neuron projection bundle disease or disorder", "disease or disorder of cranial neuron projection bundle"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cranial nerve neuropathy", "shortest_name_length": 18}
{"curie": "UMLS:C2349436", "names": ["Migraine-triggered seizure", "Migraine-Triggered Seizure", "Migraine-triggered Seizure", "Migraine triggered seizures", "migraine triggered seizures", "migraine triggered seizures (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Migraine-triggered seizure", "shortest_name_length": 26}
{"curie": "MONDO:0030602", "names": ["Klebsiella", "pneumonia; bacillus", "bacillus; pneumonia", "Pneumonia klebsiella", "KLEBSIELLA PNEUMONIA", "pneumonia klebsiella", "Klebsiella Pneumonia", "Klebsiella pneumonia", "klebsiella pneumonia", "pneumonia; Klebsiella", "Klebsiellal pneumonia", "Bacillus; Friedländer", "Klebsiella; pneumonia", "Friedlander's pneumonia", "Klebsiella caused pneumonia", "PNEUMONIA BACTERIAL KLEBSIELLA", "pneumonia; Friedländer's bacil", "Friedländer's bacil; pneumonia", "Klebsiella pneumoniae pneumonia", "pneumonia due to Klebsiella pneumonia", "pneumonia due to Klebsiella pneumoniae", "Pneumonia due to Klebsiella pneumoniae", "Pneumonia caused by Klebsiella pneumoniae", "pneumonia caused by Klebsiella pneumoniae", "pneumonia due to Klebsiella pneumonia (diagnosis)", "pneumonia due to Klebsiella pneumoniae (disorder)", "Pneumonia due to Klebsiella pneumoniae (disorder)", "Pneumonia caused by Klebsiella pneumoniae (disorder)", "Klebsiella pneumoniae [K. pneumoniae] as the cause of diseases classified to other chapters"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Klebsiella pneumonia", "shortest_name_length": 10}
{"curie": "MONDO:0060568", "names": ["PILBOS", "Pilarowski Bjornsson syndrome", "PILAROWSKI-BJORNSSON SYNDROME", "Pilarowski-Bjornsson syndrome", "developmental delay and speech apraxia with or without seizures", "DEVELOPMENTAL DELAY AND SPEECH APRAXIA WITH OR WITHOUT SEIZURES", "Intellectual disability-autism-speech apraxia-craniofacial dysmorphism syndrome", "Intellectual disability, autism, speech apraxia, craniofacial dysmorphism syndrome", "Intellectual disability, autism, speech apraxia, craniofacial dysmorphism syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pilarowski-Bjornsson syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0006917", "names": ["PCA Infarct", "PCA Infarcts", "Infarct, PCA", "Infarcts, PCA", "PCA Infarction", "Infarction, PCA", "Posterior Cerebral Artery Stroke", "Stroke, Posterior Cerebral Artery", "stroke of posterior cerebral artery", "Posterior cerebral artery infarction", "posterior cerebral artery infarction", "Posterior Cerebral Artery Infarction", "Infarction, Posterior Cerebral Artery", "stroke of posterior cerebral artery (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "posterior cerebral artery infarction", "shortest_name_length": 11}
{"curie": "MONDO:0014428", "names": ["DFNB102", "autosomal recessive deafness 102", "DEAFNESS, AUTOSOMAL RECESSIVE 102", "deafness, autosomal recessive 102", "deafness, autosomal recessive type 102", "autosomal recessive nonsyndromic deafness 102", "EPS8 autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 102", "autosomal recessive nonsyndromic deafness type 102", "autosomal recessive nonsyndromic deafness caused by mutation in EPS8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 102", "shortest_name_length": 7}
{"curie": "MONDO:0019088", "names": ["PTLD", "PTLD, NOS", "Post-transplantation lymphoproliferation", "Post-transplant lymphoproliferative disease", "post-transplant lymphoproliferative disease", "Post-Transplant Lymphoproliferative Disorder", "Post-transplant lymphoproliferative disorder", "Post-transplant Lymphoproliferative Disorder", "Post transplant lymphoproliferative disorder", "post-transplant lymphoproliferative disorder", "Post transplant lymphoproliferative disorder, NOS", "Post-transplantation lymphoproliferative syndrome", "Post-transplant lymphoproliferative disorder (PTLD)", "PTLD - Post-transplant lymphoproliferative disorder", "Lymphoproliferative disorder following transplantation", "post-transplant lymphoproliferative disease (diagnosis)", "Lymphoproliferative disorder following transplantation (disorder)", "Post-transplantation lymphoproliferation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "post-transplant lymphoproliferative disease", "shortest_name_length": 4}
{"curie": "MONDO:0006658", "names": ["Arterioloscleroses", "arteriolosclerosis", "Arteriolosclerosis", "Arteriolosclerosis, NOS", "Arteriolosclerosis (morphologic abnormality)", "arteriolosclerosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arteriolosclerosis", "shortest_name_length": 18}
{"curie": "MONDO:0000884", "names": ["myeloid and lymphoid neoplasms associated with FGFR1 abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myeloid and lymphoid neoplasms associated with FGFR1 abnormalities", "shortest_name_length": 66}
{"curie": "MONDO:0010283", "names": ["MRXSL", "trisomy Xq28", "distal duplication Xq", "XLMR syndrome, Lubs type", "telomeric duplication Xq", "Xq28 (MECP2) duplication", "MECP2 Duplication Syndrome", "MECP2 Duplication syndrome", "MECP2 DUPLICATION SYNDROME", "MECP2 duplication syndrome", "Proximal Xq28 duplication syndrome", "Mental retardation, X-linked, Lubs type", "LUBS X-LINKED MENTAL RETARDATION SYNDROME", "Lubs X-linked mental retardation syndrome", "Lubs X-Linked Mental Retardation Syndrome", "Lubs X-linked intellectual disability syndrome", "mental retardation, X-linked, Lubs type (formerly)", "mental retardation, X-linked, syndromic, Lubs type", "Lubs X-linked mental retardation syndrome (formerly)", "syndromic X-linked intellectual disability Lubs type", "X-linked intellectual disability syndrome, Lubs type", "hereditary disease X-linked MECP2 duplication syndrome", "intellectual disability, X-linked, syndromic, Lubs type", "intellectual disability, X-linked, Lubs type (formerly)", "Lubs X-linked intellectual disability syndrome (formerly)", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS-TYPE", "mental retardation, X-linked, with recurrent respiratory infections", "MENTAL RETARDATION, X-LINKED, WITH RECURRENT RESPIRATORY INFECTIONS", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE", "Mental Retardation, X-Linked, With Recurrent Respiratory Infections", "X-linked intellectual disability-hypotonia-recurrent Infections syndrome", "X-linked intellectual disability-hypotonia-recurrent infections syndrome", "intellectual disability, X-linked, with recurrent respiratory infections", "Methyl-cytosine phosphate guanine binding protein-2 duplication syndrome", "Methyl-CpG (cytosine phosphate guanine) binding protein-2 duplication syndrome", "Methyl-cytosine phosphate guanine binding protein-2 duplication syndrome (disorder)", "Methyl-cytosine phosphate guanine binding protein-2 duplication syndrome (diagnosis)", "intellectual developmental disorder, X-linked syndromic, Lubs type, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic X-linked intellectual disability Lubs type", "shortest_name_length": 5}
{"curie": "UMLS:C1265982", "names": ["Spindle cell nodule", "Postoperative spindle cell nodule", "Postoperative Spindle Cell Nodule", "Posttraumatic Spindle Cell Nodule", "Spindle cell nodule (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spindle cell nodule", "shortest_name_length": 19}
{"curie": "MONDO:0018565", "names": ["congenital urachal anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital urachal anomaly", "shortest_name_length": 26}
{"curie": "MONDO:0005788", "names": ["ET-NANBH", "hepatitis e", "e hepatitis", "hepatitis E", "Hepatitis E", "hepatitis type E", "Viral hepatitis E", "Water-Borne Hepatitis", "Hepatitis, Water-Borne", "Viral hepatitis type E", "Hepatitis, Water Borne", "Water-Borne Hepatitides", "Hepatitides, Water-Borne", "hepatitis; virus, type E", "hepatitis E virus infection", "Hepatitis E virus hepatitis", "Hepatitis E virus infection", "Epidemic non-A non-B hepatitis", "Epidemic Non-A, Non-B Hepatitis", "Epidemic Non A, Non B Hepatitis", "Fecal-oral non-A non-B hepatitis", "Viral hepatitis type E (disorder)", "Faecal-oral non-A non-B hepatitis", "Hepatitis E virus caused hepatitis", "Enterically transmitted non-A non-B hepatitis", "Enterically-Transmitted Non-A, Non-B Hepatitis", "Enterically Transmitted Non A, Non B Hepatitis", "Hepatitis, Viral, Non-A, Non-B, Enterically-Transmitted"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatitis E virus infection", "shortest_name_length": 8}
{"curie": "UMLS:C0269870", "names": ["Second degree perineal tear", "Second Degree Perineal Laceration", "Second degree perineal laceration", "Obstetrical laceration, second degree", "Laceration, obstetrical, second degree", "Second degree perineal laceration, NOS", "Second degree perineal tear during delivery", "Second degree perineal laceration (disorder)", "Second-degree perineal laceration, with delivery", "Second degree perineal laceration during delivery", "Second-degree perineal laceration during delivery", "second-degree perineal laceration during delivery", "Second degree perineal laceration (physical finding)", "post-delivery exam showing second degree perineal laceration", "second-degree perineal laceration during delivery (diagnosis)", "Laceration of inner and muscular layers of perineal structures", "post-delivery exam showing second degree laceration of perineum", "Laceration of inner AND/OR muscular layers of perineal structures", "laceration; vagina, complicating delivery, with perineum, muscles", "laceration; vagina, with perineum and muscles, complicating delivery", "laceration; perineum, second degree, complicating delivery, complicating delivery", "post-delivery exam showing second degree laceration of perineum (physical finding)", "Second-degree perineal laceration, delivered, with or without mention of antepartum condition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Second degree perineal laceration", "shortest_name_length": 27}
{"curie": "MONDO:0004327", "names": ["Sphenoid Sinus Papilloma", "Sphenoid Sinus Schneiderian Papilloma", "sphenoid sinus Schneiderian papilloma", "Schneiderian papilloma of sphenoid sinus", "Schneiderian Papilloma of Sphenoid Sinus", "Schneiderian papilloma of the sphenoid sinus", "Schneiderian Papilloma of the Sphenoid Sinus", "Schneiderian papilloma of the Sphenoid sinus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sphenoid sinus Schneiderian papilloma", "shortest_name_length": 24}
{"curie": "UMLS:C1334244", "names": ["Intracranial Chloroma", "Intracranial Myeloid Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intracranial Myeloid Sarcoma", "shortest_name_length": 21}
{"curie": "MONDO:0300000", "names": ["SSR3-CDG", "SSR3 deficiency", "SSR3 congenital disorder of glycosylation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SSR3-CDG", "shortest_name_length": 8}
{"curie": "UMLS:C5556670", "names": ["ISMC", "iSMILE", "Invasive Stratified Mucinous Carcinoma", "Invasive Stratified Mucinous Adenocarcinoma", "Cervical Invasive Stratified Mucinous Carcinoma", "Cervical Invasive Stratified Mucinous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Invasive Stratified Mucinous Adenocarcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0006752", "names": ["ERYSIPELOID", "erysipeloid", "Erysipeloid", "Erysipeloids", "Erysipeloid NOS", "Rosenbach erysipeloid", "Fish handlers' disease", "Erysipeloid (disorder)", "Erysipeloid of Rosenbach", "Erysipeloid, unspecified", "ERYSIPELOID OF ROSENBACH", "Infection due to E. rhusiopathiae", "Infection due to Erysipelothrix insidiosa", "Infection caused by Erysipelothrix insidiosa", "Infection due to Erysipelothrix rhusiopathiae", "Erysipelothrix rhusiopathiae infectious disease", "Erysipelothrix rhusiopathiae disease or disorder", "Infection caused by Erysipelothrix rhusiopathiae", "Erysipelothrix rhusiopathiae caused disease or disorder", "Infection due to Erysipelothrix rhusiopathiae (disorder)", "Infection caused by Erysipelothrix rhusiopathiae (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Erysipelothrix rhusiopathiae infectious disease", "shortest_name_length": 11}
{"curie": "MONDO:0020600", "names": ["Pharyngitis;acute", "pharyngitis acute", "PHARYNGITIS ACUTE", "Acute Pharyngitis", "Pharyngitis Acute", "Acute pharyngitis", "acute pharyngitis", "pharyngitis, acute", "pharyngitis nos acute", "Acute pharyngitis, NOS", "Pharyngitis (acute) NOS", "Acute pharyngitis (disorder)", "acute pharyngitis (diagnosis)", "Acute pharyngitis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute pharyngitis", "shortest_name_length": 17}
{"curie": "UMLS:C5447476", "names": ["Refractory Lung Non-Squamous Non-Small Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Lung Non-Squamous Non-Small Cell Carcinoma", "shortest_name_length": 53}
{"curie": "MONDO:0100457", "names": ["Familial esophageal achalasia", "ACHALASIA, FAMILIAL ESOPHAGEAL", "Achalasia, familial esophageal", "achalasia, familial esophageal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "achalasia, familial esophageal", "shortest_name_length": 29}
{"curie": "UMLS:C5419465", "names": ["Acute Myeloid Leukemia Arising from Previous Myelodysplastic/Myeloproliferative Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Myeloid Leukemia Arising from Previous Myelodysplastic/Myeloproliferative Neoplasm", "shortest_name_length": 88}
{"curie": "MONDO:0015803", "names": ["botulism wound", "Wound Botulism", "Wound botulism", "wound botulism", "botulism; wound", "Wound Botulisms", "Botulism, Wound", "wound; botulism", "Inoculation botulism", "inoculation botulism", "skin infectious botulism", "Skin infectious botulism", "Wound botulism (disorder)", "Wound botulism (diagnosis)", "skin toxin-mediated botulism", "Skin toxin-mediated botulism", "Cutaneous infectious botulism", "cutaneous infectious botulism", "Cutaneous toxin-mediated botulism", "cutaneous toxin-mediated botulism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "wound botulism", "shortest_name_length": 14}
{"curie": "MONDO:0009762", "names": ["autosomal recessive congenital nystagmus", "NYSTAGMUS, CONGENITAL, AUTOSOMAL RECESSIVE", "nystagmus, congenital, autosomal recessive", "autosomal recessive congenital motor nystagmus", "Nystagmus, Congenital Motor, Autosomal Recessive", "Nystagmus, congenital motor, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nystagmus, congenital, autosomal recessive", "shortest_name_length": 40}
{"curie": "MONDO:0006074", "names": ["Adenosquamous Carcinoma", "ADENOSQUAMOUS CARCINOMA", "Adenosquamous carcinoma", "adenosquamous carcinoma", "Adenosquamous Carcinomas", "Carcinoma, Adenosquamous", "Carcinomas, Adenosquamous", "Adenosquamous cell carcinoma", "adenosquamous cell carcinoma", "Adenosquamous carcinoma (disorder)", "CARCINOMA, ADENOSQUAMOUS, MALIGNANT", "adenosquamous carcinoma (diagnosis)", "carcinoma, adenosquamous, malignant", "mixed adenocarcinoma and squamous carcinoma", "Mixed Adenocarcinoma and Squamous Carcinoma", "Mixed adenocarcinoma and epidermoid carcinoma", "mixed adenocarcinoma and epidermoid carcinoma", "Mixed Adenocarcinoma and Epidermoid Carcinoma", "Mixed adenocarcinoma and squamous cell carcinoma", "mixed adenocarcinoma and squamous cell carcinoma", "Mixed Adenocarcinoma and Squamous Cell Carcinoma", "adenosquamous carcinoma (morphologic abnormality)", "Adenosquamous carcinoma (morphologic abnormality)", "Mixed Adenocarcinoma and Epidermoid Cell Carcinoma", "mixed adenocarcinoma and epidermoid cell carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenosquamous carcinoma", "shortest_name_length": 23}
{"curie": "UMLS:C0544840", "names": ["Amyloidoma", "amyloidoma", "Nodular Amyloidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Amyloidoma", "shortest_name_length": 10}
{"curie": "MONDO:0007114", "names": ["ASPED", "Angel shaped phalangoepiphyseal dysplasia", "ANGEL-SHAPED PHALANGOEPIPHYSEAL dysplasia", "Angel-shaped phalangoepiphyseal dysplasia", "Angel-Shaped Phalangoepiphyseal Dysplasia", "ANGEL-SHAPED PHALANGOEPIPHYSEAL DYSPLASIA", "angel-shaped phalango-epiphyseal dysplasia", "Angel-shaped phalango-epiphyseal dysplasia", "ASPED - angel-shaped phalango-epiphyseal dysplasia", "Angel-shaped phalangoepiphyseal dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angel-shaped phalango-epiphyseal dysplasia", "shortest_name_length": 5}
{"curie": "MONDO:0002223", "names": ["Ovarian Malignant Mesothelioma", "ovarian malignant mesothelioma", "ovary malignant mesothelioma (disease)", "malignant mesothelioma (disease) of ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian malignant mesothelioma", "shortest_name_length": 30}
{"curie": "MONDO:0003394", "names": ["pulp disorder", "Endodontic disease", "Dental Pulp Disease", "dental pulp disease", "Dental pulp disorder", "Dental Pulp Diseases", "Pulp Disease, Dental", "dental pulp disorder", "Dental Pulp Disorder", "Disease, Dental Pulp", "Pulp Diseases, Dental", "Diseases, Dental Pulp", "Dental pulp--Diseases", "Dental pulp disorders", "disease of dental pulp", "Endodontic disease, NOS", "disorder of dental pulp", "Disorder of pulp of tooth", "disorder of pulp of tooth", "Disease of pulp of tooth, NOS", "dental pulp disease or disorder", "disease or disorder of dental pulp", "Disorder of pulp of tooth (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dental pulp disorder", "shortest_name_length": 13}
{"curie": "MONDO:0019689", "names": ["perlecan-related bone disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "perlecan-related bone disorder", "shortest_name_length": 30}
{"curie": "MONDO:0003601", "names": ["mediastinum liposarcoma", "mediastinal liposarcoma", "lip mediastinum sarcoma", "Mediastinal Liposarcoma", "liposarcoma of mediastinum", "Liposarcoma of Mediastinum", "Liposarcoma of mediastinum", "liposarcoma of the mediastinum", "Liposarcoma of the Mediastinum", "liposarcoma of mediastinum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mediastinum liposarcoma", "shortest_name_length": 23}
{"curie": "MONDO:0060621", "names": ["NDMSCA", "NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND CORTICAL ATROPHY", "neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy", "shortest_name_length": 6}
{"curie": "MONDO:0013395", "names": ["RP4", "RP 4", "Retinitis Pigmentosa 4", "retinitis pigmentosa 4", "RETINITIS PIGMENTOSA 4", "RHO retinitis pigmentosa", "retinitis pigmentosa type 4", "Retinitis Pigmentosa, Rhodopsin-Related", "RETINITIS PIGMENTOSA, RHODOPSIN-RELATED", "retinitis pigmentosa, rhodopsin-related", "retinitis pigmentosa caused by mutation in RHO", "retinitis pigmentosa 4, autosomal dominant or recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 4", "shortest_name_length": 3}
{"curie": "UMLS:C4725786", "names": ["Intestinal T-Cell Lymphoma, NOS", "Intestinal T-Cell Lymphoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal T-Cell Lymphoma, Not Otherwise Specified", "shortest_name_length": 31}
{"curie": "UMLS:C1276137", "names": ["Lymphoepithelial tumor of skin", "Lymphoepithelial tumour of skin", "Skin Lymphoepithelioma-Like Carcinoma", "Lymphoepithelioma-like carcinoma of skin", "Lymphoepithelial tumor of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoepithelial tumor of skin", "shortest_name_length": 30}
{"curie": "MONDO:0016369", "names": ["RTS2", "Rothmund Thomson syndrome type 2", "Rothmund-Thomson Syndrome Type 2", "Rothmund-Thomson syndrome type 2", "ROTHMUND-THOMSON SYNDROME, TYPE 2", "Rothmund-Thomson syndrome, type 2", "Poikiloderma of Rothmund-Thomson type 2", "poikiloderma of Rothmund-Thomson type 2", "Rothmund Thomson syndrome type 2 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rothmund-Thomson syndrome type 2", "shortest_name_length": 4}
{"curie": "MONDO:0001935", "names": ["Charcot joint", "CHARCOT JOINT", "charcot joint", "Charcot Joint", "Charcots Joint", "Charcot joints", "charcots joint", "charcot joints", "charcots joints", "Charcot's Joint", "Charcot's joint", "Charcôt's joint", "charcot's joint", "charcot's joints", "Joint, Charcot's", "neuropathic joint", "Neuropathic joint", "NEUROPATHIC JOINT", "Neuropathic joints", "joints neuropathic", "charcot arthropathy", "Charcot arthropathy", "arthropathy charcots", "charcot's arthropathy", "neuropathic arthritis", "Charcot's arthropathy", "Arthropathy neurogenic", "arthropathy neurogenic", "ARTHROPATHY NEUROGENIC", "neurogenic arthropathy", "Arthritis, neuropathic", "Neurogenic Arthropathy", "Neurogenic arthropathy", "charcot's joint disease", "Arthropathy, Neurogenic", "Neuropathic arthropathy", "neuropathic arthropathy", "arthropathy neuropathic", "NEUROPATHIC ARTHROPATHY", "Charcot's joint disease", "Neurogenic Arthropathies", "ARTHROPATHY, NEUROPATHIC", "Arthropathies, Neurogenic", "neuropathic joint disease", "JOINT DISEASE, NEUROPATHIC", "Charcot's joint was observed", "neurogenic arthropathy charcot", "Charcot's arthropathy (disorder)", "Neurogenic arthropathy of Charcot", "Charcot's arthropathy (diagnosis)", "Charcot's joint (physical finding)", "neuropathic joint disease (diagnosis)", "neuropathic arthropathy (& Charcot's)", "NEUROGENIC OSTEOARTHROPATHY CHARCOT JOINTS", "NEUROGENIC OSTEOARTHROPATHY <CHARCOT JOINTS>", "Arthropathy associated with neurological disorder", "arthropathy associated with neurological disorder", "Arthropathy associated with neurological disorders", "Arthropathy associated with a neurological disorder", "Arthropathy associated with a neurological disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurogenic arthropathy", "shortest_name_length": 13}
{"curie": "MONDO:0015374", "names": ["PCNSV", "PACNS", "primary CNS vasculitis", "Granulomatous Angiitis of CNS", "primary central nervous system vasculitis", "Granulomatous angiitis of the nervous system", "primary angiitis of the central nervous system", "isolated angiitis of the central nervous system", "primary vasculitis of the central nervous system", "Granulomatous angiitis of central nervous system", "Granulomatous Angiitis of the Central Nervous System", "granulomatous angiitis of the central nervous system", "GACNS - granulomatous angiitis of central nervous system", "Granulomatous angiitis of central nervous system (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary central nervous system vasculitis", "shortest_name_length": 5}
{"curie": "UMLS:C3671688", "names": ["Cyclic Leucopenia", "Cyclic Hematopoesis", "Periodic Neutropenia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cyclic Hematopoesis", "shortest_name_length": 17}
{"curie": "MONDO:0005242", "names": ["Empyema", "EMPYEMA", "empyema", "Empyema NOS", "Empyema, NOS", "Pleural Empyema", "collection of pus", "Empyema (disorder)", "Empyema (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "empyema", "shortest_name_length": 7}
{"curie": "MONDO:0011639", "names": ["DBA15", "RPS28 Diamond-Blackfan anemia", "Diamond-Blackfan anemia caused by mutation in RPS28", "Diamond-Blackfan Anemia With Microtia And Cleft Palate", "Diamond Blackfan anemia 15 with mandibulofacial dysostosis", "Diamond-Blackfan anemia 15 with mandibulofacial dysostosis", "DIAMOND-BLACKFAN ANEMIA 15 WITH MANDIBULOFACIAL DYSOSTOSIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diamond-Blackfan anemia 15 with mandibulofacial dysostosis", "shortest_name_length": 5}
{"curie": "MONDO:0002406", "names": ["eczema", "dermatitis", "Dermatitis", "DERMATITIS", "dermatitides", "Dermatitides", "Skin inflamed", "Dermatitis NOS", "Dermatitis, NOS", "DERMATITIS (NOS)", "Skin Inflammation", "skin inflammation", "Skin inflammation", "Steroid dermatitis", "inflammation; skin", "skin; inflammation", "Skin--Inflammation", "inflammation of skin", "Inflammation of Skin", "Skin inflammation NOS", "SKIN INFLAMMATION NOS", "Cutaneous inflammation", "dermatitis (diagnosis)", "Dermatitis, unspecified", "Inflammatory dermatosis", "inflammation of the skin", "Inflammation of the Skin", "Inflammatory skin disease", "zone of skin inflammation", "Inflammation of skin, NOS", "inflammatory skin disease", "inflammation of zone of skin", "Skin Inflammation/ Irritation", "Inflammatory dermatosis (disorder)", "Inflammatory abnormality of the skin", "Abnormal tendency to infections of the skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermatitis", "shortest_name_length": 6}
{"curie": "MONDO:0014891", "names": ["HNFJ4", "ADTKD5", "ADTKD-SEC61A1", "hyperuricemic nephropathy, familial juvenile, 4", "hyperuricemic NEPHROPATHY, familial juvenile, 4", "HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 4", "SEC61A1 familial juvenile hyperuricemic nephropathy", "hyperuricemic nephropathy, familial juvenile type 4", "hyperuricemic nephropathy, familial juvenile, type 4", "tubulointerstitial kidney disease, autosomal dominant, 5", "TUBULOINTERSTITIAL KIDNEY DISEASE, AUTOSOMAL DOMINANT, 5", "SEC61A1-related autosomal dominant tubulointerstitial kidney disease", "familial juvenile hyperuricemic nephropathy caused by mutation in SEC61A1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperuricemic nephropathy, familial juvenile type 4", "shortest_name_length": 5}
{"curie": "UMLS:C0334620", "names": ["Diffuse Malignant Lymphoma", "Diffuse malignant lymphoma", "Malignant lymphoma, diffuse", "Malignant lymphoma, diffuse NOS", "Malignant lymphoma, diffuse, NOS", "MALIGNANT LYMPHOMA, NOS, OR DIFFUSE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant lymphoma, diffuse", "shortest_name_length": 26}
{"curie": "MONDO:0018744", "names": ["Oligodendroglial tumor", "oligodendroglial tumor", "Oligodendroglial Tumor", "oligodendroglial neoplasm", "Oligodendroglial Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oligodendroglial tumor", "shortest_name_length": 22}
{"curie": "UMLS:C0175167", "names": ["RASH ACNEFORM", "Rash acneiform", "RASH ACNEIFORM", "acneform eruption", "Acneiform eruption", "Acneiform Eruption", "Acneform eruptions", "acneiform eruption", "Acneiform Eruptions", "Eruption, Acneiform", "Eruptions, Acneiform", "Acneiform eruption (disorder)", "acneiform eruption (physical finding)", "clinical impressions acneiform eruption"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acneiform Eruptions", "shortest_name_length": 13}
{"curie": "MONDO:0005441", "names": ["otitis Media", "otitis media", "Otitis media", "OTITIS MEDIA", "Otitis Media", "media otitis", "media; otitis", "Medial Otitis", "medial otitis", "medias otitis", "otitis; media", "Otitis media NOS", "otitis media nos", "Otitis media, NOS", "OM - Otitis media", "catarrh; middle ear", "middle ear; catarrh", "middle ear infection", "Middle ear infection", "infection; middle ear", "Catarrh of middle ear", "middle ear; infection", "otitis media (disease)", "otitis or otitis media", "middle Ear Inflammation", "Middle Ear Inflammation", "Otitis media (disorder)", "middle ear inflammation", "Middle ear inflammation", "otitis media (diagnosis)", "Inflammation, Middle Ear", "inflammation; middle ear", "middle ear; inflammation", "Unspecified otitis media", "Otitis media, unspecified", "inflammation of middle ear", "Otitis media, unspecified, unspecified ear", "middle ear inflammation (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "otitis media", "shortest_name_length": 12}
{"curie": "MONDO:0014512", "names": ["MRD31", "NEDRIHF", "MRD31, FORMERLY", "autosomal dominant mental retardation 31", "mental retardation, autosomal dominant 31", "autosomal dominant intellectual disability 31", "intellectual disability, autosomal dominant 31", "mental retardation, autosomal dominant type 31", "intellectual disability, autosomal dominant type 31", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 31, FORMERLY", "autosomal dominant intellectual developmental disorder 31", "autosomal dominant non-syndromic intellectual disability 31", "PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation", "NEURODEVELOPMENTAL DISORDER WITH NEONATAL RESPIRATORY INSUFFICIENCY, HYPOTONIA, AND FEEDING DIFFICULTIES", "neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation", "shortest_name_length": 5}
{"curie": "UMLS:C0795688", "names": ["INTRACRANIAL SUBARACHNOID HEMORRHAGE", "Intracranial Subarachnoid Hemorrhage", "Hemorrhage, Intracranial Subarachnoid", "Intracranial Subarachnoid Hemorrhages", "Subarachnoid Hemorrhage, Intracranial", "Subarachnoid Hemorrhages, Intracranial", "Hemorrhages, Intracranial Subarachnoid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subarachnoid Hemorrhage, Intracranial", "shortest_name_length": 36}
{"curie": "MONDO:0006798", "names": ["hypervitaminosis A", "Hypervitaminosis A", "HYPERVITAMINOSIS A", "A-hypervitaminosis", "A; hypervitaminosis", "hypervitaminosis; A", "hypervitaminosis type A", "vitamin A; hyperalimentation", "hyperalimentation; vitamin A", "Hypervitaminosis A (disorder)", "hypervitaminosis A (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypervitaminosis A", "shortest_name_length": 18}
{"curie": "UMLS:C0740380", "names": ["Varicella zoster", "zoster varicella", "varicella zoster", "VARICELLA ZOSTER"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Varicella zoster", "shortest_name_length": 16}
{"curie": "MONDO:0005475", "names": ["Migraine aura", "migraine aura", "aura migraine", "aura migraines", "migraine auras", "aura; migraine", "migraine; aura", "auras migraines", "classic migraine", "Classic migraine", "Classic Migraine", "classic migraines", "Migraine, Classic", "Classical migraine", "Migraine;classical", "Migraine with aura", "Classical Migraine", "migraine classical", "Migraine with Aura", "migraine with aura", "Migraine With Aura", "classical migraine", "migraine; classical", "classical; migraine", "Migraine with Auras", "Migraine, Classical", "Migraine with aura NOS", "Migraine with typical aura", "Migraine with Typical Aura", "classical migraine with aura", "Migraine with aura (disorder)", "classic migraine with typical aura", "Migraine with typical aura (disorder)", "Migraine with aura [classical migraine]", "classical migraine with aura (diagnosis)", "classic migraine with typical aura (diagnosis)", "Migraine preceded or accompanied by transient focal neurological phenomena"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "migraine with aura", "shortest_name_length": 13}
{"curie": "UMLS:C0153710", "names": ["Lymphosarcoma, spleen", "Lymphosarcoma of spleen", "lymphosarcoma of spleen", "Lymphosarcoma involving spleen", "Lymphosarcoma Involving Spleen", "Lymphosarcoma of spleen (disorder)", "lymphosarcoma of spleen (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphosarcoma of spleen", "shortest_name_length": 21}
{"curie": "MONDO:0011597", "names": ["ATOD3", "atopic dermatitis 3", "Dermatitis, Atopic, 3", "dermatitis, ATOPIC, 3", "DERMATITIS, ATOPIC, 3", "dermatitis, atopic, 3", "atopic dermatitis type 3", "atopic dermatitis with asthma", "dermatitis, Atopic, with asthma", "Dermatitis, Atopic, with Asthma", "DERMATITIS, ATOPIC, WITH ASTHMA", "dermatitis, atopic, susceptibility to, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermatitis, atopic, 3", "shortest_name_length": 5}
{"curie": "UMLS:C0854843", "names": ["Relapsed Intestinal T-Cell Lymphoma", "Intestinal T-cell lymphoma recurrent", "Recurrent Intestinal T-Cell Lymphoma", "Recurrent Enteropathy-Associated T-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal T-cell lymphoma recurrent", "shortest_name_length": 35}
{"curie": "UMLS:C0920646", "names": ["renal ischemia", "ischemia renal", "Renal ischemia", "kidney ischemia", "Renal ischaemia", "ischemia; kidney", "kidney; ischemic", "Ischemia of kidney", "Ischaemia of kidney", "renal ischemia (diagnosis)", "Ischemia of kidney (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ischemia of kidney", "shortest_name_length": 14}
{"curie": "UMLS:C2609166", "names": ["Discordant twin", "Discordant Twin", "Discordant Growth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Discordant twin", "shortest_name_length": 15}
{"curie": "MONDO:0009658", "names": ["MPS3D", "MPS 3D", "MPSIIID", "MPS 3 D", "MPS IIID", "MPS IIIDs", "MPS III D", "Sanfilippo D", "GNS deficiency", "Sanfilippo syndrome D", "Sanfilippo Syndrome D", "Sanfilippo D syndrome", "SANFILIPPO SYNDROME D", "Sanfilippo syndrome type D", "Sanfilippo syndrome, type D", "Mucopolysaccharidosis III-D", "mucopolysaccharidosis type 3D", "Mucopolysaccharidosis type 3D", "Mucopoly-saccharidosis type 3D", "mucopolysaccharidosis, type 3D", "Mucopolysaccharidosis Type 3 D", "Mucopolysaccharidosis Type IIID", "Mucopolysaccharidosis type IIID", "mucopolysaccharidosis type IIID", "mucopolysaccharidosis, type IIID", "Mucopolysaccharidosis Type IIIDs", "MUCOPOLYSACCHARIDOSIS, TYPE IIID", "Mucopolysaccharidosis, MPS-III-D", "Mucopolysaccharidosis III-D (disorder)", "MPS III-D - Mucopolysaccharidosis III-D", "MPSIIID - Mucopolysaccharidosis type IIID", "N Acetylglucosamine 6 Sulfatase Deficiency", "N-Acetylglucosamine-6-Sulfatase Deficiency", "N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY", "N-Acetylglucosamine-6-sulfatase deficiency", "N-acetylglucosamine-6-sulfatase deficiency", "Glucosamine N-acetyl-6-sulfatase deficiency", "N-Acetylglucosamine-6-sulphatase deficiency", "glucosamine N-acetyl-6-sulfatase deficiency", "Deficiency, N-Acetylglucosamine-6-Sulfatase", "N-acetylglucosamine-6-sulphatase deficiency", "N-Acetylglucosamine-6-Sulfatase Deficiencies", "Deficiencies, N-Acetylglucosamine-6-Sulfatase", "Deficiency of N-acetylglucosamine-6-sulfatase", "Deficiency of N-acetylglucosamine-6-sulphatase", "N Acetylglucosamine 6 Sulfate Sulfatase Deficiency", "N-Acetylglucosamine-6-Sulfate Sulfatase Deficiency", "N-acetylglucosamine-6-sulfate sulfatase deficiency", "Sulfatase Deficiency, N-Acetylglucosamine-6-Sulfate", "Deficiency, N-Acetylglucosamine-6-Sulfate Sulfatase", "N-Acetylglucosamine-6-Sulfate Sulfatase Deficiencies", "Sulfatase Deficiencies, N-Acetylglucosamine-6-Sulfate", "Deficiencies, N-Acetylglucosamine-6-Sulfate Sulfatase"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucopolysaccharidosis type 3D", "shortest_name_length": 5}
{"curie": "UMLS:C3266992", "names": ["EGFR gene mutation", "ERBB Gene Mutation", "EGFR Gene Mutation", "HER1 Gene Mutation", "ERBB1 Gene Mutation", "Epidermal Growth Factor Receptor Gene Mutation", "Epidermal growth factor receptor gene mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "EGFR gene mutation", "shortest_name_length": 18}
{"curie": "UMLS:C1336196", "names": ["Stage IIB Squamous Cell Lung Cancer", "Stage IIB Squamous Cell Lung Carcinoma", "Stage IIB Squamous Cell Carcinoma of Lung", "Stage IIB Squamous Cell Carcinoma of the Lung", "Stage IIB Lung Squamous Cell Carcinoma AJCC v7", "Stage IIB Squamous Cell Lung Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Lung Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 35}
{"curie": "UMLS:C0276143", "names": ["viral sore throat", "viral pharyngitis", "PHARYNGITIS VIRAL", "Viral pharyngitis", "Viral sore throat", "VIRAL PHARYNGITIS", "pharyngitis viral", "pharyngitis; viral", "virus; pharyngitis", "virus; sore throat", "sore throats viral", "sore throat; viral", "Pharyngitis viral NOS", "Viral sore throat NOS", "Viral pharyngitis, NOS", "Viral pharyngitis (disorder)", "Viral pharyngitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Viral pharyngitis", "shortest_name_length": 17}
{"curie": "MONDO:0018155", "names": ["PLS", "Adult-onset PLS", "adult-onset PLS", "lateral sclerosis", "Lateral Sclerosis", "Lateral Scleroses", "lateral; sclerosis", "Scleroses, Lateral", "sclerosis; lateral", "Sclerosis, Lateral", "Primary lateral sclerosis", "primary lateral sclerosis", "Primary Lateral Scleroses", "Primary Lateral Sclerosis", "Sclerosis, Primary Lateral", "Lateral Sclerosis, Primary", "Lateral Scleroses, Primary", "Scleroses, Primary Lateral", "SCLEROSIS, PRIMARY, LATERAL", "Primary lateral sclerosis (disorder)", "Adult-onset primary lateral sclerosis", "adult-onset primary lateral sclerosis", "primary lateral sclerosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lateral sclerosis", "shortest_name_length": 3}
{"curie": "UMLS:C5205875", "names": ["CARDIOVASCULAR RADIATION INJURY", "Cardiovascular Radiation Injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiovascular Radiation Injury", "shortest_name_length": 31}
{"curie": "MONDO:0012684", "names": ["ARVD12", "ARVC12", "arrhythmogenic right ventricular dysplasia 12", "Arrhythmogenic Right Ventricular Cardiomyopathy 12", "ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 12", "arrhythmogenic right ventricular cardiomyopathy 12", "arrhythmogenic right ventricular dysplasia type 12", "familial arrhythmogenic right ventricular dysplasia 12", "Arrhythmogenic Right Ventricular Dysplasia, Familial, 12", "ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 12", "arrhythmogenic right ventricular dysplasia, familial, 12", "arrhythmogenic right ventricular dysplasia, familial, type 12", "JUP familial isolated arrhythmogenic right ventricular dysplasia", "familial isolated arrhythmogenic right ventricular dysplasia caused by mutation in JUP"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arrhythmogenic right ventricular dysplasia 12", "shortest_name_length": 6}
{"curie": "UMLS:C4682658", "names": ["Stage III Gestational Trophoblastic Neoplasm AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Gestational Trophoblastic Neoplasm AJCC v8", "shortest_name_length": 52}
{"curie": "MONDO:0018225", "names": ["ALK-DLBCL", "ALK+ LBCL", "ALK+ large B-cell lymphoma", "ALK positive large B-cell lymphoma", "ALK-positive large B-cell lymphoma", "ALK-Positive Large B-Cell Lymphoma", "Anaplastic lymphoma kinase positive large B-cell lymphoma", "Diffuse Large B-Cell Lymphoma with Expression of Full-Length ALK", "diffuse large B-cell lymphoma with expression of full-length ALK", "Anaplastic lymphoma kinase positive large B-cell lymphoma (disorder)", "Anaplastic lymphoma kinase positive large B-cell lymphoma (diagnosis)", "Anaplastic lymphoma kinase positive large B-cell lymphoma (morphologic abnormality)", "Diffuse Large B-Cell Lymphoma with Expression of Full-Length Anaplastic Lymphoma Kinase", "diffuse large B-cell lymphoma with expression of full-length anaplastic lymphoma kinase"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ALK-positive large B-cell lymphoma", "shortest_name_length": 9}
{"curie": "UMLS:C0577731", "names": ["Disseminated adenocarcinoma", "Disseminated Adenocarcinoma", "Disseminated adenocarcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disseminated adenocarcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0003040", "names": ["retrograde amnesia", "Retrograde Amnesia", "AMNESIA RETROGRADE", "Retrograde amnesia", "Retrograde Amnesias", "amnesia; retrograde", "Amnesia, Retrograde", "retrograde; amnesia", "Amnesias, Retrograde", "RA - Retrograde amnesia", "Retrograde amnesia (finding)", "Retrograde memory impairment", "retrograde amnesia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retrograde amnesia", "shortest_name_length": 18}
{"curie": "UMLS:C1512260", "names": ["grade I meningioma", "Grade I Meningioma", "Grade 1 Meningioma", "WHO Grade 1 Meningioma", "WHO Grade I Meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade I Meningioma", "shortest_name_length": 18}
{"curie": "MONDO:0000925", "names": ["hyperlucent lung", "Hyperlucent Lung", "hyperlucent lungs", "Hyperlucent Lungs", "Lung, Hyperlucent", "Lungs, Hyperlucent", "Hyperlucent Thorax", "Thorax, Hyperlucent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperlucent lung", "shortest_name_length": 16}
{"curie": "MONDO:0008142", "names": ["THIEMANN DISEASE", "THIEMANN disease", "Thiemann's disease", "OSTEOARTHROPATHY, DIGITAL", "Thiemann epiphyseal disease", "THIEMANN EPIPHYSEAL DISEASE", "Thiemann disease, familial form", "osteoarthropathy of fingers familial", "Osteoarthropathy of fingers familial", "osteoarthropathy of fingers, familial", "Osteoarthropathy Of Fingers, Familial", "OSTEOARTHROPATHY OF FINGERS, FAMILIAL", "Osteochondrosis of phalangeal epiphyses", "osteochondritis of phalangeal epiphyses", "aseptic necrosis of phalangeal epiphyses", "Aseptic necrosis of phalangeal epiphyses", "Familial osteoarthropathy of the fingers", "Osteoarthropathy of the fingers, familial", "Familial osteoarthropathy of the fingers (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thiemann disease, familial form", "shortest_name_length": 16}
{"curie": "MONDO:0002243", "names": ["bleeding disorder", "bleeding tendency", "Bleeding Tendency", "Bleeding Disorder", "bleeding diathesis", "Bleeding diathesis", "Bleeding Diathesis", "hemorrhage; disease", "disease; hemorrhage", "hemorrhagic disease", "Hemorrhagic diseases", "hemorrhagic disorder", "HEMORRHAGIC DISORDER", "hemorrhagic diseases", "Hemorrhagic disorder", "Hemorrhagic Disorder", "hemorrhagic; disease", "hemorrhagic disorders", "Haemorrhagic disorder", "Hemorrhagic Diathesis", "HAEMORRHAGIC DISORDER", "hemorrhagic diathesis", "Hemorrhagic Disorders", "Disorder, Hemorrhagic", "hemorrhagic condition", "Hemorrhagic Diatheses", "Hemorrhagic diathesis", "Disorders, Hemorrhagic", "Diatheses, Hemorrhagic", "Haemorrhagic diathesis", "diathesis; hemorrhagic", "Haemorrhagic disorders", "hemorrhagic; diathesis", "conditions hemorrhagic", "Diathesis, Hemorrhagic", "Bleeding Predisposition", "bleeding predisposition", "Coagulation abnormality", "Coagulation abnormalities", "Blood coagulation disorder", "Abnormality of coagulation", "hemorrhagic condition (diagnosis)", "Unspecified hemorrhagic conditions", "Hemorrhagic condition, unspecified", "Abnormal blood coagulation studies", "Haemorrhagic condition, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemorrhagic disease", "shortest_name_length": 17}
{"curie": "UMLS:C2981364", "names": ["stage IIB gastric cancer", "Stage IIB Gastric Cancer", "stage IIB gastric cancer AJCC v7", "Stage IIB Gastric Cancer AJCC v7", "Stage IIB Gastric (Stomach) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Gastric Cancer AJCC v7", "shortest_name_length": 24}
{"curie": "UMLS:C5237307", "names": ["Refractory Thyroid Gland Follicular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Thyroid Gland Follicular Carcinoma", "shortest_name_length": 45}
{"curie": "UMLS:C4744527", "names": ["Temporal Lobe Pleomorphic Xanthoastrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Temporal Lobe Pleomorphic Xanthoastrocytoma", "shortest_name_length": 43}
{"curie": "MONDO:0003850", "names": ["Clivus Chondroid Chordoma", "clivus chondroid chordoma", "Chondroid Chordoma of Clivus", "chondroid chordoma of clivus", "Chondroid Chordoma of the Clivus", "chondroid chordoma of the clivus", "clivus of occipital bone chondroid chordoma", "chondroid chordoma of clivus of occipital bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "clivus chondroid chordoma", "shortest_name_length": 25}
{"curie": "MONDO:0003256", "names": ["neurohypophysis granular cell tumor", "Granular Cell Tumor of Neurohypophysis", "granular cell tumor of neurohypophysis", "granular cell tumor of Neurohypophysis", "Granular cell tumor of neurohypophysis", "Granular cell tumour of neurohypophysis", "Granular Cell Tumor of the Sellar Region", "granular cell tumor of the sellar region", "Granular cell tumor of the sellar region", "Granular cell tumor of posterior pituitary", "Granular Cell Tumor of the Neurohypophysis", "granular cell tumor of the neurohypophysis", "Granular cell tumour of posterior pituitary", "Granular cell tumor of neurohypophysis (disorder)", "granular cell tumor of the posterior pituitary gland", "Granular Cell Tumor of the Posterior Pituitary Gland", "Granular Cell Tumor of the Neurohypophysis (WHO Grade 1)", "Granular Cell Tumor of the Neurohypophysis (WHO Grade I)", "granular cell tumor of the Neurohypophysis (WHO grade I)", "Granular Cell Tumour of the Sellar Region/Granular Cell Pituicytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurohypophysis granular cell tumor", "shortest_name_length": 35}
{"curie": "UMLS:C0334248", "names": ["Squamous cell carcinoma, nonkeratinizing", "Non-keratinizing squamous cell carcinoma", "Non-keratinising squamous cell carcinoma", "Squamous cell carcinoma, nonkeratinising", "Squamous cell carcinoma, nonkeratinizing, NOS", "Squamous cell carcinoma, non-keratinizing type", "Epidermoid carcinoma, large cell, nonkeratinizing", "Epidermoid carcinoma, large cell, nonkeratinising", "Non-keratinizing epidermoid carcinoma - large cell", "nonkeratinizing large cell squamous cell carcinoma", "Non-keratinising epidermoid carcinoma - large cell", "Non-Keratinizing Large Cell Squamous Cell Carcinoma", "large cell, nonkeratinizing squamous cell carcinoma", "Squamous cell carcinoma, large cell, nonkeratinizing", "Squamous cell carcinoma, large cell, nonkeratinising", "Non-keratinizing squamous cell carcinoma - large cell", "Non-keratinising squamous cell carcinoma - large cell", "Epidermoid carcinoma, large cell, non-keratinizing type", "Squamous cell carcinoma, large cell, non-keratinizing type", "nonkeratinizing large cell squamous cell carcinoma (diagnosis)", "Squamous cell carcinoma, large cell, nonkeratinizing (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Squamous cell carcinoma, large cell, nonkeratinizing", "shortest_name_length": 40}
{"curie": "UMLS:C1333856", "names": ["Grade 3 Colorectal Adenocarcinoma", "Grade III Colorectal Adenocarcinoma", "High Grade Colorectal Adenocarcinoma", "Poorly Differentiated Colorectal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade 3 Colorectal Adenocarcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0012175", "names": ["ARCC1", "CTRCT28", "cataract 28", "CATARACT 28", "cataract type 28", "age-related cortical cataract 1", "CATARACT, AGE-RELATED CORTICAL, 1", "cataract, age-related cortical, 1", "Cataract, Age-Related Cortical, 1", "cataract 28, age-related cortical, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 28", "shortest_name_length": 5}
{"curie": "MONDO:0008650", "names": ["Faulk-Epstein-Jones syndrome", "Faulk Epstein Jones syndrome", "Vertebral fusion posterior lumbosacral blepharoptosis", "vertebral fusion posterior lumbosacral blepharoptosis", "VERTEBRAL FUSION, POSTERIOR LUMBOSACRAL, WITH BLEPHAROPTOSIS", "vertebral fusion, POSTERIOR lumbosacral, with blepharoptosis", "Vertebral Fusion, Posterior Lumbosacral, With Blepharoptosis", "congenital ptosis and posterior fusion of lumbosacral vertebrae", "Congenital ptosis and posterior fusion of lumbosacral vertebrae", "Posterior fusion of lumbosacral vertebrae-blepharoptosis syndrome", "familial posterior lumbosacral vertebral fusion and eyelid ptosis", "Familial posterior lumbosacral vertebral fusion and eyelid ptosis", "posterior fusion of lumbosacral vertebrae-blepharoptosis syndrome", "Posterior fusion of lumbosacral vertebrae and blepharoptosis syndrome", "Posterior fusion of lumbosacral vertebrae and blepharoptosis syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "posterior fusion of lumbosacral vertebrae-blepharoptosis syndrome", "shortest_name_length": 28}
{"curie": "UMLS:C5244004", "names": ["BRASH syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "BRASH syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C5446817", "names": ["Vitreoretinal Disease", "Vitreoretinal Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vitreoretinal Disorder", "shortest_name_length": 21}
{"curie": "MONDO:0014664", "names": ["JBTS23", "JOUBERT SYNDROME 23", "Joubert syndrome 23", "Joubert syndrome type 23", "KIAA0586 Joubert syndrome", "Joubert syndrome caused by mutation in KIAA0586"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome 23", "shortest_name_length": 6}
{"curie": "UMLS:C4683148", "names": ["Stage II Posterior Uveal Melanoma AJCC v8", "Stage II Choroidal and Ciliary Body Melanoma", "Stage II Choroidal and Ciliary Body Melanoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Choroidal and Ciliary Body Melanoma AJCC v8", "shortest_name_length": 41}
{"curie": "UMLS:C0729245", "names": ["Acute peptic ulcer", "acute peptic ulcer", "peptic; ulcer, acute", "ulcer; peptic, acute", "Acute peptic ulcer (disorder)", "acute peptic ulcer (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute peptic ulcer (disorder)", "shortest_name_length": 18}
{"curie": "UMLS:C0016397", "names": ["Focal infection", "focal infection", "Focal Infection", "infection focal", "Infection, Focal", "infection; focal", "Focal Infections", "focal; infection", "focal infections", "Infections, Focal", "localize infection", "Localized infection", "Localised infection", "INFECTION LOCALIZED", "INFECTION LOCALISED", "Infection localised", "localized infection", "Infection localized", "Infection, localized", "Localized infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Focal Infection", "shortest_name_length": 15}
{"curie": "UMLS:C0016738", "names": ["Frottage", "frottage", "frotteurism", "Frotteurism", "Frotteurism (disorder)", "frotteurism (diagnosis)", "sexual; deviation, frotteurism", "deviation; sexual, frotteurism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Frotteurism", "shortest_name_length": 8}
{"curie": "UMLS:C4520772", "names": ["Gallbladder Cancer Stage 0", "Stage 0 Gallbladder Cancer", "Stage 0 Gallbladder Carcinoma", "Gallbladder Carcinoma in situ", "Carcinoma in situ of Gallbladder", "Stage 0 Carcinoma of Gallbladder", "Stage 0 Gallbladder Cancer AJCC v7", "Stage 0 Gallbladder Cancer AJCC v6", "Carcinoma in situ of the Gallbladder", "Stage 0 Carcinoma of the Gallbladder", "stage 0 gallbladder carcinoma in situ", "Stage 0 Gallbladder Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Gallbladder Cancer AJCC v6 and v7", "shortest_name_length": 26}
{"curie": "MONDO:0015259", "names": ["Stratton-Garcia-Young syndrome", "brachydactyly-mesomelia-intellectual disability-heart defects syndrome", "brachydactyly mesomelia mental retardation aortic dilatation mitral valve prolapse and characteristic face", "brachydactyly mesomelia intellectual disability aortic dilatation mitral valve prolapse and characteristic face"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly-mesomelia-intellectual disability-heart defects syndrome", "shortest_name_length": 30}
{"curie": "MONDO:0011029", "names": ["MLRL", "myeloid tumor suppressor", "MYELOID TUMOR SUPPRESSOR", "MYELOID LEUKEMIA-RELATED LOCUS", "myeloid leukemia-related locus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myeloid tumor suppressor", "shortest_name_length": 4}
{"curie": "MONDO:0001163", "names": ["Paranoid Personality", "paranoid personality", "Paranoid personality", "paranoid; personality", "personality; paranoid", "Personality, Paranoid", "Paranoid Personalities", "Personalities, Paranoid", "Paranoid Personality Disorder", "paranoid personality disorder", "PERSONALITY DISORDER PARANOID", "Paranoid personality disorder", "disorder paranoid personality", "Personality Disorder, Paranoid", "paranoid personality disorders", "Disorder, Paranoid Personality", "Paranoid Personality Disorders", "personality disorder; paranoid", "paranoid; personality disorder", "Disorders, Paranoid Personality", "Paranoid personality (disorder)", "Personality Disorders, Paranoid", "Paranoid personality disorder (disorder)", "paranoid personality disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paranoid personality disorder", "shortest_name_length": 20}
{"curie": "MONDO:0003805", "names": ["Pericardial Mesothelioma", "pericardium mesothelioma", "pericardial mesothelioma", "Pericardial mesothelioma", "mesothelioma; pericardium", "pericardium; mesothelioma", "Mesothelioma of pericardium", "malignant Pericardial Mesothelioma", "Pericardial Malignant Mesothelioma", "pericardial malignant mesothelioma", "Pericardial mesothelioma malignant", "malignant pericardial mesothelioma", "malignant mesothelioma of pericardium", "Malignant mesothelioma of pericardium", "Malignant Mesothelioma of Pericardium", "malignant mesothelioma of the pericardium", "Malignant Mesothelioma of the Pericardium", "Advanced Pericardial Malignant Mesothelioma", "Pericardial mesothelioma malignant advanced", "Pericardial Mesothelioma Malignant Advanced", "pericardium malignant mesothelioma (disease)", "malignant neoplasm mesothelioma of pericardium", "malignant mesothelioma (disease) of pericardium", "Malignant mesothelioma of pericardium (disorder)", "malignant mesothelioma of pericardium (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant pericardial mesothelioma", "shortest_name_length": 24}
{"curie": "UMLS:C5206715", "names": ["Unresectable Lung Non-Squamous Non-Small Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Lung Non-Squamous Non-Small Cell Carcinoma", "shortest_name_length": 55}
{"curie": "UMLS:C3805012", "names": ["Ectopic pregnancy with contraceptive device"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ectopic pregnancy with contraceptive device", "shortest_name_length": 43}
{"curie": "UMLS:C1333040", "names": ["Chronic Lymphocytic Leukemia with Plasmacytoid Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic Lymphocytic Leukemia with Plasmacytoid Differentiation", "shortest_name_length": 62}
{"curie": "UMLS:C0205671", "names": ["arenavirus infection", "Arenavirus Infection", "Arenavirus Infections", "Infection, Arenavirus", "Infections, Arenavirus", "arenavirus infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infections, Arenavirus", "shortest_name_length": 20}
{"curie": "MONDO:0032703", "names": ["SSASKS", "short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis", "SHORT STATURE, AMELOGENESIS IMPERFECTA, AND SKELETAL DYSPLASIA WITH SCOLIOSIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis", "shortest_name_length": 6}
{"curie": "MONDO:0004744", "names": ["preglaucoma", "Preglaucoma", "Preglaucoma, NOS", "borderline glaucoma", "Borderline glaucoma", "borderline; glaucoma", "glaucoma; borderline", "preglaucoma (diagnosis)", "Preglaucoma, unspecified", "Borderline glaucoma, NOS", "Borderline glaucoma (glaucoma suspect)", "Borderline glaucoma [glaucoma suspect]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "borderline glaucoma", "shortest_name_length": 11}
{"curie": "MONDO:0012692", "names": ["RENAL TUBULAR ACIDOSIS, DISTAL, WITH NEPHROCALCINOSIS, SHORT STATURE, MENTAL RETARDATION, AND DISTINCTIVE FACIES", "Renal Tubular Acidosis, Distal, With Nephrocalcinosis, Short Stature, Mental Retardation, And Distinctive Facies", "renal tubular acidosis, distal, with nephrocalcinosis, short stature, mental retardation, and distinctive facies", "renal tubular acidosis, distal, with nephrocalcinosis, short stature, intellectual disability, and distinctive facies", "RENAL TUBULAR ACIDOSIS, DISTAL, WITH NEPHROCALCINOSIS, SHORT STATURE, IMPAIRED INTELLECTUAL DEVELOPMENT, AND DISTINCTIVE FACIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal tubular acidosis, distal, with nephrocalcinosis, short stature, intellectual disability, and distinctive facies", "shortest_name_length": 112}
{"curie": "MONDO:0016243", "names": ["Hb E-disease", "Hb-E disease", "Homozygous for Hb E", "hemoglobin e disease", "HEMOGLOBIN E DISEASE", "Hemoglobin E disease", "Hemoglobin E Disease", "hemoglobin E disease", "Haemoglobin E disease", "Hemoglobin E-E disease", "diseases e haemoglobin", "Haemoglobin E-E disease", "Homozygous hemoglobin E", "Homozygous haemoglobin E", "hemoglobin E (Hb-E) disease", "Hemoglobin E disease (disorder)", "hemoglobin E (Hb-E) disease (diagnosis)", "hemoglobinopathy hemoglobin E (Hb-E) disease", "disease (or disorder); hemoglobin or Hb, E (Hb-E)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemoglobin E disease", "shortest_name_length": 12}
{"curie": "UMLS:C4726597", "names": ["Pelvic Rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pelvic Rhabdomyosarcoma", "shortest_name_length": 23}
{"curie": "UMLS:C0269102", "names": ["Endometrioma", "endometrioma", "endometriomas", "Endometriomas", "Chocolate cyst", "chocolate cyst", "chocolate cysts", "chocolate; cyst", "cyst; chocolate", "endometriotic cyst", "Endometriotic cyst", "cysts endometriotic", "Cyst, endometriotic", "Ovarian Endometrioma", "Endometrioma of Ovary", "Endometrioma of ovary", "ovary; cyst, chocolate", "Ovarian chocolate cyst", "Chocolate cyst of ovary", "chocolate cyst of ovary", "Endometrioma of the Ovary", "Ovarian Endometriotic Cyst", "'Chocolate' cysts of ovary", "Endometriotic Cyst of Ovary", "endometriotic cyst of ovary", "Ovarian endometriotic cysts", "Endometriotic cyst of ovary", "Endometrial cystoma of ovary", "Endometriotic Cyst of the Ovary", "cyst; ovary, ovarian, chocolate", "Endometrioid cystadenoma of ovary", "Chocolate cyst of ovary (disorder)", "chocolate cyst of ovary (diagnosis)", "Endometriotic cyst (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endometrioma", "shortest_name_length": 12}
{"curie": "UMLS:C5238929", "names": ["Steroid Resistant Gastrointestinal Tract Acute Graft Versus Host Disease", "Steroid Refractory Gastrointestinal Tract Acute Graft Versus Host Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Steroid Resistant Gastrointestinal Tract Acute Graft Versus Host Disease", "shortest_name_length": 72}
{"curie": "UMLS:C2585890", "names": ["Nonsquamous nonsmall cell neoplasm of lung", "Nonsquamous non-small cell neoplasm of lung", "non-squamous non-small cell neoplasm of lung", "lung malignant carcinoma non-small cell non-squamous", "Nonsquamous nonsmall cell neoplasm of lung (disorder)", "non-squamous non-small cell neoplasm of lung (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nonsquamous nonsmall cell neoplasm of lung", "shortest_name_length": 42}
{"curie": "UMLS:C5670007", "names": ["TOXICITY_INFUSION", "Infusion Related Toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infusion Related Toxicity", "shortest_name_length": 17}
{"curie": "MONDO:0001283", "names": ["Endosalpingiosis", "endosalpingiosis", "Endosalpingiosis (disorder)", "Peritoneal Endosalpingiosis", "endosalpingiosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endosalpingiosis", "shortest_name_length": 16}
{"curie": "MONDO:0100500", "names": ["Mendelian neurodevelopmental disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mendelian neurodevelopmental disorder", "shortest_name_length": 37}
{"curie": "MONDO:0018681", "names": ["neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome", "shortest_name_length": 90}
{"curie": "MONDO:0033009", "names": ["GAMOS5", "Galloway-Mowat syndrome 5", "GALLOWAY-MOWAT SYNDROME 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Galloway-Mowat syndrome 5", "shortest_name_length": 6}
{"curie": "UMLS:C1868998", "names": ["Cytotoxic edema", "Cytotoxic oedema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cytotoxic edema", "shortest_name_length": 15}
{"curie": "MONDO:0014679", "names": ["NEDSPLB", "PMGYCHA", "polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis", "POLYMICROGYRIA, PERISYLVIAN, WITH CEREBELLAR HYPOPLASIA AND ARTHROGRYPOSIS", "NEURODEVELOPMENTAL DISORDER WITH SPASTICITY, HYPOMYELINATING LEUKODYSTROPHY, AND BRAIN ABNORMALITIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis", "shortest_name_length": 7}
{"curie": "MONDO:0008479", "names": ["SMDCF", "Sutcliffe SmD", "spondylometaphyseal dysplasia Sutcliffe type", "spondylometaphyseal dysplasia, Sutcliffe type", "SPONDYLOMETAPHYSEAL DYSPLASIA, SUTCLIFFE TYPE", "Spondylometaphyseal dysplasia, Sutcliffe type", "Spondylometaphyseal Dysplasia, Sutcliffe Type", "Spondylometaphyseal dysplasia - Sutcliffe type", "Sutcliffe type of spondylometaphyseal dysplasia", "spondylometaphyseal dysplasia corner fracture type", "SPONDYLOMETAPHYSEAL DYSPLASIA, CORNER FRACTURE TYPE", "spondylometaphyseal dysplasia, corner fracture type", "Spondylometaphyseal Dysplasia, Corner Fracture Type", "spondylometaphyseal dysplasia, 'corner fracture' type", "Spondylometaphyseal dysplasia, 'corner fracture' type", "Spondylometaphyseal dysplasia - Sutcliffe type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondylometaphyseal dysplasia, 'corner fracture' type", "shortest_name_length": 5}
{"curie": "UMLS:C1266103", "names": ["Mixed Testicular Sex Cord-Stromal Tumor", "Sex cord-gonadal stromal tumor, mixed forms", "Sex Cord-Gonadal Stromal Tumor, Mixed Forms", "Sex cord-gonadal stromal tumour, mixed forms", "Mixed Testicular Sex Cord-Gonadal Stromal Tumor", "Testicular Sex Cord-Gonadal Stromal Tumor, Mixed Forms", "Sex cord-gonadal stromal tumor, mixed forms (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular Sex Cord-Gonadal Stromal Tumor, Mixed Forms", "shortest_name_length": 39}
{"curie": "MONDO:0011825", "names": ["streptococcus, group A, severity of infection by", "STREPTOCOCCUS, GROUP A, SEVERITY OF INFECTION BY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "streptococcus, group A, severity of infection by", "shortest_name_length": 48}
{"curie": "MONDO:0032937", "names": ["MYOPMIL", "congenital myopathy 9B", "MYOPATHY, CONGENITAL PROXIMAL, WITH MINICORE LESIONS", "myopathy, congenital proximal, with minicore lesions", "MYOPATHY, CONGENITAL, PROXIMAL, WITH MINICORE LESIONS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy, congenital proximal, with minicore lesions", "shortest_name_length": 7}
{"curie": "UMLS:C5556494", "names": ["Muscle Invasive Bladder Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Muscle Invasive Bladder Urothelial Carcinoma", "shortest_name_length": 44}
{"curie": "UMLS:C1335147", "names": ["Osteolytic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Osteolytic Neoplasm", "shortest_name_length": 19}
{"curie": "UMLS:C1708195", "names": ["Gastric Soft Tissue Tumor", "Gastric Soft Tissue Neoplasm", "Soft Tissue Tumor of Stomach", "Soft Tissue Neoplasm of Stomach", "Soft Tissue Tumor of the Stomach", "Soft Tissue Neoplasm of the Stomach"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Soft Tissue Neoplasm", "shortest_name_length": 25}
{"curie": "MONDO:0033669", "names": ["NS13", "Noonan Syndrome 13", "NOONAN SYNDROME 13", "Noonan syndrome 13"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Noonan syndrome 13", "shortest_name_length": 4}
{"curie": "UMLS:C4744333", "names": ["Locally Advanced Unresectable Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Unresectable Carcinoma", "shortest_name_length": 39}
{"curie": "MONDO:0009452", "names": ["VICIS", "VICI SYNDROME", "Vici Syndrome", "Vici syndrome", "Vici syndrome (disorder)", "Vici syndrome (diagnosis)", "congenital malformation syndromes Vici", "Dionisi Vici Sabetta Gambarara syndrome", "Dionisi-Vici-Sabetta-Gambarara syndrome", "absent corpus callosum cataract immunodeficiency", "Absent corpus callosum cataract immunodeficiency", "absent corpus callosum-cataract-immunodeficiency syndrome", "corpus callosum agenesis-cataract-immunodeficiency syndrome", "Corpus callosum agenesis-cataract-immunodeficiency syndrome", "immunodeficiency with cleft lip/palate, cataract, hypopigmentation and absent corpus callosum", "IMMUNODEFICIENCY WITH CLEFT LIP/PALATE, CATARACT, HYPOPIGMENTATION, AND ABSENT CORPUS CALLOSUM", "immunodeficiency with cleft Lip/palate, cataract, hypopigmentation, and absent corpus callosum", "immunodeficiency with cleft lip/palate, cataract, hypopigmentation, and absent corpus callosum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vici syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0011203", "names": ["CAMPOMELIC DYSPLASIA, MILD", "Campomelic dysplasia, mild", "campomelic dysplasia, mild", "SKELETAL DYSPLASIA RELATED TO CAMPOMELIC DYSPLASIA", "skeletal dysplasia related to campomelic dysplasia", "Pierre Robin sequence with pectus excavatum and rib and scapular anomalies", "PIERRE ROBIN SEQUENCE WITH PECTUS EXCAVATUM AND RIB AND SCAPULAR ANOMALIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pierre Robin sequence with pectus excavatum and rib and scapular anomalies", "shortest_name_length": 26}
{"curie": "MONDO:0008252", "names": ["platelet adenylate cyclase activity", "PLATELET ADENYLATE CYCLASE ACTIVITY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "platelet adenylate cyclase activity", "shortest_name_length": 35}
{"curie": "UMLS:C3888580", "names": ["MBO", "Malignant bowel obstruction", "Malignant Bowel Obstruction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Bowel Obstruction", "shortest_name_length": 3}
{"curie": "UMLS:C1833102", "names": ["DIABETES MELLITUS, PERMANENT NEONATAL, WITH NEUROLOGIC FEATURES", "Diabetes Mellitus, Permanent Neonatal, With Neurologic Features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DIABETES MELLITUS, PERMANENT NEONATAL, WITH NEUROLOGIC FEATURES", "shortest_name_length": 63}
{"curie": "MONDO:0043875", "names": ["Tumor Lysis Syndrome", "tumor lysis syndrome", "TUMOR LYSIS SYNDROME", "Tumor lysis syndrome", "tumor lysis syndromes", "Syndrome, Tumor Lysis", "tumour lysis syndrome", "Tumour lysis syndrome", "Tumor Lysis Syndromes", "syndrome, tumor lysis", "Tumour Lysis Syndrome", "TUMOUR LYSIS SYNDROME", "tumour lysis syndromes", "syndromes, tumor lysis", "Tumour Lysis Syndromes", "Syndromes, Tumor Lysis", "Syndrome, Tumour Lysis", "syndrome, tumour lysis", "syndromes, tumour lysis", "Syndromes, Tumour Lysis", "Tumor lysis syndrome (disorder)", "tumor lysis syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tumor lysis syndrome", "shortest_name_length": 20}
{"curie": "MONDO:0000430", "names": ["PTCL", "T-cell lymphoma", "T-Zone Lymphoma", "T-zone lymphoma", "T-zone; lymphoma", "lymphoma; T-zone", "NK-T cell lymphoma", "Mature T-cell lymphoma", "mature T-cell lymphoma", "mature NK/T-cell lymphoma", "Mature T/NK-cell lymphomas", "peripheral t-cell lymphoma", "peripheral t cell lymphoma", "T-zone lymphoma (disorder)", "peripheral T-cell lymphoma", "Peripheral T-Cell Lymphoma", "T-zone lymphoma (clinical)", "Peripheral T-cell lymphoma", "Peripheral T Cell Lymphoma", "cell lymphomas peripheral t", "Peripheral T-Cell Lymphomas", "T Cell Lymphoma, Peripheral", "T-Cell Lymphoma, Peripheral", "T-zone lymphoma (diagnosis)", "peripheral; T-cell lymphoma", "lymphoma; peripheral T-cell", "Lymphoma, Peripheral T-Cell", "Lymphoma, T-Cell, Peripheral", "Lymphomas, Peripheral T-Cell", "T-cell; lymphoma, peripheral", "lymphoma; T-cell, peripheral", "Lymphoma, T Cell, Peripheral", "T-Cell Lymphomas, Peripheral", "Mature T-and NK-Cell Lymphoma", "mature T-and NK-cell lymphoma", "Peripheral T-cell lymphoma NOS", "Peripheral T-Cell Lymphoma, NOS", "Peripheral T-cell lymphoma, NOS", "Mature T- and NK-Cell Lymphomas", "peripheral T-cell lymphoma, NOS", "mature T-cell lymphoma (diagnosis)", "mature T-cell and NK-cell lymphoma", "Mature T-Cell and NK-Cell Lymphoma", "mature T-cell non-Hodgkin's lymphoma", "Mature T-Cell Non-Hodgkin's Lymphoma", "mature NK/T-cell lymphoma (diagnosis)", "Peripheral T-cell lymphoma (clinical)", "Peripheral T-cell lymphoma (disorder)", "Peripheral T-Cell Lymphoma, Large Cell", "Peripheral T-cell lymphoma unspecified", "Peripheral T-cell lymphoma (diagnosis)", "Peripheral T-cell lymphoma, large cell", "Mature T/NK-cell lymphomas, unspecified", "T-Zone Variant Peripheral T-Cell Lymphoma", "Peripheral T-cell lymphoma unspecified NOS", "Mature T-Cell and NK-Cell Non-Hodgkin Lymphoma", "mature T-cell and natural killer cell lymphoma", "mature T-cell and NK-cell non-Hodgkin lymphoma", "mature T-cell and NK-cell non-Hodgkin's lymphoma", "Primary cutaneous peripheral T-cell lymphoma NOS", "Mature T-Cell and NK-Cell Non-Hodgkin's Lymphoma", "Peripheral T-cell lymphoma pleomorphic small cell", "Peripheral T-cell lymphoma, pleomorphic small cell", "Peripheral T-Cell Lymphoma, Not Otherwise Specified", "Peripheral T-cell lymphoma - pleomorphic small cell", "peripheral T-cell lymphoma, not otherwise specified", "Peripheral T-cell lymphoma (morphologic abnormality)", "lymphoma; peripheral T-cell, pleomorphic, small cell", "peripheral; T-cell lymphoma, pleomorphic, small cell", "lymphoma; T-cell, peripheral, pleomorphic, small cell", "T-cell; lymphoma, peripheral, pleomorphic, small cell", "Primary cutaneous unspecified peripheral T-cell lymphoma", "Peripheral T-cell lymphoma pleomorphic medium and large cell", "Peripheral T-cell lymphoma, pleomorphic medium and large cell", "Peripheral T-cell lymphoma, pleomorphic small cell (diagnosis)", "Peripheral T-cell lymphoma - pleomorphic medium and large cell", "peripheral; T-cell lymphoma, pleomorphic, medium and large cell", "lymphoma; peripheral T-cell, pleomorphic, medium and large cell", "lymphoma; T-cell, peripheral, pleomorphic, medium and large cell", "T-cell; lymphoma, peripheral, pleomorphic, medium and large cell", "Primary cutaneous peripheral T-cell lymphoma not otherwise specified", "Peripheral T-cell lymphoma, pleomorphic medium and large cell (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mature T-cell and NK-cell non-Hodgkin lymphoma", "shortest_name_length": 4}
{"curie": "MONDO:0033946", "names": ["HAE1", "HANE", "ANGIOEDEMA, HEREDITARY, 1", "hereditary angioedema type I", "Hereditary angioedema type I", "Hereditary Angioedema Type I", "angioedema, hereditary, type 1", "ANGIOEDEMA, HEREDITARY, TYPE I", "angioedema, hereditary, type 2", "angioedema, hereditary, type I", "Angioedema, Hereditary, Type I", "ANGIONEUROTIC EDEMA, HEREDITARY", "angioedema, hereditary, 1 and 2", "angioneurotic edema, hereditary", "C1 ESTERASE INHIBITOR DEFICIENCY", "angioedema, hereditary, type 1/2", "C1 esterase inhibitor, deficiency of", "hereditary angioedema with C1Inh deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary angioedema with C1Inh deficiency", "shortest_name_length": 4}
{"curie": "UMLS:C1328061", "names": ["MDS/MPD-U", "MDS/MPN-U", "MDS/MPN, U", "MDS/MPD, U", "Myeloproliferative neoplasm, unclassifiable", "Unclassified myelodysplastic/myeloproliferative disease", "Unclassifiable Myelodysplastic/Myeloproliferative Disease", "Myelodysplastic/Myeloproliferative Disease, Unclassifiable", "Unclassifiable Myeloproliferative/Myelodysplastic Syndrome", "Myelodysplastic/myeloproliferative neoplasm, unclassifiable", "Myelodysplastic/Myeloproliferative Neoplasm, Unclassifiable", "myelodysplastic/myeloproliferative neoplasm, unclassifiable", "Unclassified mixed myelodysplastic/myeloproliferatic syndrome", "Mixed Myelodysplastic/Myeloproliferative Disease, Unclassifiable", "Mixed Myeloproliferative/Myelodysplastic Syndrome, Unclassifiable", "Myelodysplastic/myeloproliferative neoplasm, unclassifiable (disorder)", "myelodysplastic/myeloproliferative neoplasm, unclassifiable (diagnosis)", "Myelodysplastic/myeloproliferative neoplasm, unclassifiable (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myelodysplastic/myeloproliferative neoplasm, unclassifiable", "shortest_name_length": 9}
{"curie": "MONDO:0001647", "names": ["Benign renovascular hypertension", "benign renovascular hypertension", "secondary hypertension renovascular benign", "benign renovascular hypertension (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign renovascular hypertension", "shortest_name_length": 32}
{"curie": "UMLS:C1334419", "names": ["Low-Grade Sarcoma", "Low Grade Sarcoma", "Well or Moderately Differentiated Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Grade Sarcoma", "shortest_name_length": 17}
{"curie": "MONDO:0002495", "names": ["colon signet ring adenocarcinoma", "Colonic Signet Ring adenocarcinoma", "colonic signet Ring adenocarcinoma", "Colon Signet-Ring Cell Adenocarcinoma", "colon signet ring cell adenocarcinoma", "Colon Signet Ring Cell Adenocarcinoma", "Signet Ring Cell Colon Adenocarcinoma", "signet Ring cell colon adenocarcinoma", "colon signet Ring cell adenocarcinoma", "Colonic Signet Ring Cell Adenocarcinoma", "colonic signet Ring cell adenocarcinoma", "Signet Ring Cell Adenocarcinoma of Colon", "Signet-ring cell adenocarcinoma of colon", "signet Ring cell adenocarcinoma of colon", "signet Ring cell adenocarcinoma of the colon", "Signet Ring Cell Adenocarcinoma of the Colon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colon signet ring cell adenocarcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0018112", "names": ["isolated scaphocephaly", "isolated dolichocephaly", "non-syndromic sagittal synostosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated scaphocephaly", "shortest_name_length": 22}
{"curie": "UMLS:C0555971", "names": ["oral infection", "infection oral", "Oral infection", "ORAL INFECTION", "Infection mouth", "infections oral", "Oral infections", "Infection;mouth", "mouth infection", "infection mouth", "infections mouth", "Oral cavity infection", "infection of the mouth", "Oral infection (disorder)", "mouth infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral infection", "shortest_name_length": 14}
{"curie": "MONDO:0015728", "names": ["trisomy 15qter", "distal trisomy 15q", "distal duplication 15q", "distal trisomy type 15q", "telomeric duplication 15q", "Partial Duplication 15q Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal trisomy 15q", "shortest_name_length": 14}
{"curie": "MONDO:0008801", "names": ["ANOSMIA FOR ISOBUTYRIC ACID", "anosmia for isobutyric acid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anosmia for isobutyric acid", "shortest_name_length": 27}
{"curie": "UMLS:C4745160", "names": ["Resectable Intrahepatic Cholangiocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Intrahepatic Cholangiocarcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0012903", "names": ["DFNB45", "autosomal recessive deafness 45", "DEAFNESS, AUTOSOMAL RECESSIVE 45", "deafness, autosomal recessive 45", "autosomal recessive nonsyndromic deafness 45", "autosomal recessive nonsyndromic hearing loss 45", "autosomal recessive nonsyndromic deafness type 45"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 45", "shortest_name_length": 6}
{"curie": "MONDO:0002926", "names": ["chordoid sarcoma", "clear cell sarcoma", "Clear cell sarcoma", "Clear Cell Sarcoma", "Clear Cell Sarcomas", "Sarcoma, Clear Cell", "Sarcomas, Clear Cell", "Melanoma of Soft Parts", "Melanoma of soft tissue", "Melanoma of the Soft Parts", "clear cell sarcoma (diagnosis)", "clear cell sarcoma - not kidney", "Clear cell sarcoma - not kidney", "malignant melanoma of soft parts", "Malignant Melanoma of Soft Parts", "Clear Cell Sarcoma of Soft Parts", "Clear cell sarcoma of soft Parts", "clear cell sarcoma of soft parts", "Clear Cell Sarcoma of Soft Tissue", "Clear cell sarcoma of soft tissue", "Malignant melanoma of soft tissue", "clear cell sarcoma of soft tissue", "malignant melanoma of soft tissue", "Melanoma, Malignant, of Soft Parts", "Malignant melanoma of soft tissues", "malignant melanoma of soft tissues", "Melanoma, malignant, of soft parts", "melanoma, malignant, of soft parts", "adult soft part clear cell sarcoma", "malignant melanoma of the soft parts", "Adult Clear Cell Sarcoma of Soft Parts", "soft tissue neoplasm malignant melanoma", "Adult Clear Cell Sarcoma of Soft Tissue", "Clear cell sarcoma (morphologic abnormality)", "clear cell sarcoma (morphologic abnormality)", "Malignant melanoma of soft tissues (disorder)", "clear cell sarcoma of soft tissue (diagnosis)", "malignant melanoma of soft tissue (diagnosis)", "Clear cell sarcoma (except of kidney M8964/3)", "Clear cell sarcoma (except of Kidney M-89643)", "Clear cell sarcoma of the tendons and aponeuroses", "clear cell sarcoma/malignant melanoma of soft parts (excluding clear cell sarcoma of the kidney)", "Clear cell sarcoma/Malignant melanoma of soft parts (excluding Clear cell sarcoma of the kidney)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "clear cell sarcoma", "shortest_name_length": 16}
{"curie": "MONDO:0022414", "names": ["acro cephalo synostosis", "allain-babin-demarquez syndrome", "craniosynostosis synostoses hypertensive nephropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "allain-babin-demarquez syndrome", "shortest_name_length": 23}
{"curie": "UMLS:C0009353", "names": ["Colles", "colle fracture", "COLLES FRACTURE", "Colles Fracture", "colles fracture", "Fracture;Colles", "Fracture Colles'", "fracture; Colles", "Colles' fracture", "Colles' Fracture", "colles' fracture", "colles fractures", "Colles; fracture", "Fracture, Colles'", "Colles' fracture (disorder)", "Colles' fracture (diagnosis)", "fracture of radius distal end Colles'"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colles' Fracture", "shortest_name_length": 6}
{"curie": "UMLS:C2363768", "names": ["Drug delivery system malfunction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drug delivery system malfunction", "shortest_name_length": 32}
{"curie": "MONDO:0020123", "names": ["Metabolic Myopathy", "metabolic myopathy", "Metabolic myopathy", "metabolic myopathies", "Metabolic myopathy (disorder)", "Myopathy in metabolic diseases", "myopathies in metabolic diseases", "myopathies in metabolic diseases (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metabolic myopathy", "shortest_name_length": 18}
{"curie": "UMLS:C0796665", "names": ["childhood extragonadal germ cell tumor", "pediatric extragonadal germ cell tumor", "Extragonadal Malignant Germ Cell Tumor", "extragonadal germ cell tumor, pediatric", "extragonadal germ cell tumor, childhood", "germ cell tumor, extragonadal, childhood", "germ cell tumor, extragonadal, pediatric", "Childhood Extragonadal Malignant Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Extragonadal Malignant Germ Cell Tumor", "shortest_name_length": 38}
{"curie": "MONDO:0031446", "names": ["FHCA1", "Familial hypercholanemia", "Hypercholanemia, Familial", "BILE ACID, ELEVATED SERUM", "hereditary hypercholanemia", "Hereditary hypercholanemia", "HYPERCHOLANEMIA, FAMILIAL 1", "hypercholanemia, familial 1", "Familial hypercholanemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypercholanemia, familial 1", "shortest_name_length": 5}
{"curie": "UMLS:C0079740", "names": ["high-grade lymphoma", "High-Grade Lymphoma", "High Grade Lymphoma", "High-Grade Lymphomas", "Lymphoma, High-Grade", "Lymphoma, High Grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Lymphoma", "shortest_name_length": 19}
{"curie": "MONDO:0008508", "names": ["thumbs, stiff", "Thumbs, Stiff", "THUMBS, STIFF", "symphalangism, C. S. Lewis type", "Symphalangism, C. S. Lewis Type", "SYMPHALANGISM, C. S. LEWIS TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "symphalangism, C. S. Lewis type", "shortest_name_length": 13}
{"curie": "MONDO:0035445", "names": ["Chronic MCL", "chronic mast cell leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic mast cell leukemia", "shortest_name_length": 11}
{"curie": "MONDO:0002532", "names": ["Squamous Cell Tumor", "squamous cell tumor", "Squamous cell tumor", "cell squamous tumors", "Squamous cell tumour", "Epidermoid cell tumor", "epidermoid cell tumor", "Epidermoid Cell Tumor", "squamous cell neoplasm", "Squamous cell neoplasm", "Squamous Cell Neoplasm", "Cell Neoplasm, Squamous", "Squamous Cell Neoplasms", "SQUAMOUS CELL NEOPLASMS", "Neoplasm, Squamous Cell", "Neoplasms, Squamous Cell", "epidermoid cell neoplasm", "Cell Neoplasms, Squamous", "Epidermoid Cell Neoplasm", "squamous cell tumor (qualifier value)", "Squamous cell neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "squamous cell neoplasm", "shortest_name_length": 19}
{"curie": "MONDO:0023209", "names": ["hyperprolactinaemia", "galactorrhea-hyperprolactinemia", "Galactorrhea-Hyperprolactinemia", "Galactorrhoea-Hyperprolactinaemia", "galactorrhoea-hyperprolactinaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "galactorrhoea-hyperprolactinaemia", "shortest_name_length": 19}
{"curie": "MONDO:0003661", "names": ["PBL", "Breast Lymphoma", "breast lymphoma", "lymphoma of breast", "Lymphoma of Breast", "lymphoma of the breast", "Lymphoma of the Breast", "Lymphoma of the breast", "Primary breast lymphoma", "Primary Breast Lymphoma", "primary breast lymphoma", "Malignant lymphoma of breast", "malignant lymphoma of breast", "Malignant lymphoma of breast (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast lymphoma", "shortest_name_length": 3}
{"curie": "MONDO:0021579", "names": ["femur tumor", "tumor of femur", "femur neoplasm", "neoplasm of femur", "femur neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplasm of femur", "shortest_name_length": 11}
{"curie": "MONDO:0018561", "names": ["Precocious female puberty", "Precocious puberty, females", "precocious puberty in female", "Precocious puberty in female", "Precocious puberty in females", "female organism precocious puberty", "Precocious female puberty (disorder)", "precocious puberty of female organism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "precocious puberty in female", "shortest_name_length": 25}
{"curie": "UMLS:C1321872", "names": ["stage IV melanoma", "melanoma, stage IV", "Stage IV Skin Melanoma", "stage IV cutaneous melanoma", "cutaneous melanoma, stage IV", "melanoma, cutaneous stage IV", "Metastatic Cutaneous Melanoma", "metastatic cutaneous melanoma", "melanoma, cutaneous metastatic", "cutaneous melanoma, metastatic", "malignant melanoma of skin stage IV", "malignant melanoma of skin stage IV (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Skin Melanoma", "shortest_name_length": 17}
{"curie": "UMLS:C1622814", "names": ["adult DSC lymphoma", "DSC lymphoma, adult", "DLPD lymphoma, adult", "PDL, diffuse lymphocytic, adult", "Diffuse Small Cleaved Cell Lymphoma", "Adult Diffuse Small Cleaved Cell Lymphoma", "adult diffuse small cleaved cell lymphoma", "diffuse small cleaved cell lymphoma, adult", "small cleaved cell lymphoma, diffuse, adult", "lymphoma, diffuse small cleaved cell, adult", "Adult Diffuse Poorly Differentiated Cell Lymphoma", "poorly-differentiated lymphoma, diffuse lymphocytic, adult", "diffuse lymphocytic, poorly-differentiated lymphoma, adult", "lymphoma, diffuse lymphocytic, poorly-differentiated, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Diffuse Small Cleaved Cell Lymphoma", "shortest_name_length": 18}
{"curie": "UMLS:C2828201", "names": ["Stage II Bone Cancer", "Stage II Bone Cancer AJCC v7", "Stage II Bone Cancer  AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Bone Cancer AJCC v7", "shortest_name_length": 20}
{"curie": "MONDO:0013824", "names": ["JBTS17", "Joubert syndrome 17", "Joubert Syndrome 17", "JOUBERT SYNDROME 17", "Joubert syndrome type 17", "CPLANE1 Joubert syndrome", "Joubert syndrome caused by mutation in CPLANE1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome 17", "shortest_name_length": 6}
{"curie": "MONDO:0011189", "names": ["ARVC4", "ARVD4", "arrhythmogenic right ventricular dysplasia 4", "arrhythmogenic right ventricular dysplasia type 4", "ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 4", "arrhythmogenic right ventricular cardiomyopathy 4", "Arrhythmogenic Right Ventricular Cardiomyopathy 4", "fanilial arrhythmogenic right ventricular dysplasia 4", "familial arrhythmogenic right ventricular dysplasia 4", "ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 4", "Arrhythmogenic Right Ventricular Dysplasia, Familial, 4", "arrhythmogenic right ventricular dysplasia, familial, 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arrhythmogenic right ventricular dysplasia 4", "shortest_name_length": 5}
{"curie": "MONDO:0006864", "names": ["necrotizing sialometaplasia", "Necrotizing Sialometaplasia", "Necrotizing sialometaplasia", "Necrotising sialometaplasia", "Necrotizing Sialometaplasias", "Sialometaplasia, Necrotizing", "sialometaplasia; necrotizing", "Sialometaplasias, Necrotizing", "Necrotizing sialometaplasia (disorder)", "necrotizing sialometaplasia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "necrotizing sialometaplasia", "shortest_name_length": 27}
{"curie": "MONDO:0024378", "names": ["ASPS", "advanced sleep phase syndrome", "Advanced Sleep Phase Syndrome", "sleep-wake schedule disorder, advanced phase type", "Sleep-wake schedule disorder, advanced phase type", "Circadian rhythm sleep disorder, advanced sleep phase", "circadian rhythm sleep disorder, advanced sleep phase", "sleep disorder circadian rhythm, advanced sleep phase type", "Circadian rhythm sleep disorder, advanced sleep phase type", "circadian rhythm sleep disorder, advanced sleep phase type", "Sleep-wake schedule disorder, advanced phase type (disorder)", "Circadian rhythm sleep disorder, advanced sleep phase type (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "circadian rhythm sleep disorder, advanced sleep phase type", "shortest_name_length": 4}
{"curie": "MONDO:0007716", "names": ["HBHR", "ATR 16 syndrome", "ATR-16 syndrome", "ATR-16 SYNDROME", "ATR-16 Syndrome", "ATR, deletion-type", "ATR, DELETION-TYPE", "ATR syndrome, deletion type", "chromosome 16P deletion syndrome", "CHROMOSOME 16p DELETION SYNDROME", "ATR syndrome linked to chromosome 16", "mental retardation with Hemoglobin H", "Mental Retardation with Hemoglobin H", "MENTAL RETARDATION WITH HEMOGLOBIN H", "alpha thalassemia-retardation syndrome", "hemoglobin H-related mental retardation", "Hemoglobin H-related mental retardation", "Hemoglobin H-Related Mental Retardation", "HEMOGLOBIN H-RELATED MENTAL RETARDATION", "Hb H disease-mental retardation syndrome", "intellectual disability with Hemoglobin H", "Hemoglobin H-related intellectual disability", "Alpha thalassemia-mental retardation syndrome", "Alpha thalassaemia-mental retardation syndrome", "hemoglobin H disease-mental retardation syndrome", "Alpha thalassemia-intellectual disability syndrome", "alpha-thalassemia/mental retardation syndrome, type 1", "alpha thalassemia-intellectual disability syndrome type 1", "alpha-thalassemia/intellectual disability syndrome, type 1", "alpha-thalassemia/mental retardation syndrome, deletion-type", "Alpha-Thalassemia Mental Retardation Syndrome, Deletion-Type", "alpha-thalassemia/mental retardation syndrome, deletion type", "Alpha-thalassemia/mental retardation syndrome, deletion-type", "ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, DELETION-TYPE", "alpha thalassemia-intellectual disability syndrome, deletion type", "Alpha-thalassemia/intellectual disability syndrome, deletion-type", "alpha-thalassemia/intellectual disability syndrome, deletion-type", "Alpha thalassemia intellectual disability syndrome, deletion type", "Alpha thalassemia-intellectual disability syndrome, deletion type", "Alpha thalassaemia intellectual disability syndrome, deletion type", "ALPHA-thalassemia/mental retardation syndrome, chromosome 16-related", "ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED", "ALPHA-thalassemia/intellectual disability syndrome, chromosome 16-related", "Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16", "Alpha-thalassemia intellectual disability syndrome linked to chromosome 16", "alpha-thalassemia-intellectual disability syndrome linked to chromosome 16", "alpha-thalassemia intellectual disability syndrome linked to chromosome 16", "ALPHA-THALASSEMIA/IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME, DELETION TYPE", "Alpha-thalassaemia intellectual disability syndrome linked to chromosome 16", "Alpha-thalassemia-intellectual disability syndrome linked to chromosome type 16", "Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder)", "alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (diagnosis)", "alpha-thalassemia/mental retardation syndrome, deletion type (ATR, deletion. ATR1, ATR-16)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alpha thalassemia-intellectual disability syndrome type 1", "shortest_name_length": 4}
{"curie": "MONDO:0003346", "names": ["CNS Vasculitis", "cns vasculitis", "vasculitis cns", "CNS vasculitis", "Vasculitis, CNS", "angiitis cerebral", "cerebral angiitis", "Cerebral Angiitis", "Angiitis, Cerebral", "Cerebral vasculitis", "Vasculitis cerebral", "cerebral vasculitis", "VASCULITIS CEREBRAL", "Cerebral Vasculitis", "CEREBRAL VASCULITIS", "Vasculitis, Cerebral", "Cerebral vasculitis (disorder)", "cerebral vasculitis (diagnosis)", "Central Nervous System Angiitis", "Angiitis, Central Nervous System", "Central nervous system vasculitis", "central nervous system vasculitis", "Central Nervous System Vasculitis", "Vasculitis, Central Nervous System", "vasculitis of central nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system vasculitis", "shortest_name_length": 14}
{"curie": "MONDO:0014426", "names": ["NNO4", "Nanophthalmia 4", "nanophthalmos 4", "NANOPHTHALMIA 4", "NANOPHTHALMOS 4", "nanophthalmos type 4", "TMEM98 nanophthalmia", "nanophthalmia caused by mutation in TMEM98"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nanophthalmos 4", "shortest_name_length": 4}
{"curie": "UMLS:C3203639", "names": ["Neuroendocrine carcinoma metastatic", "Metastatic Neuroendocrine Carcinoma", "Neuroendocrine carcinoma, metastatic", "Neuroendocrine carcinoma, metastatic (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neuroendocrine carcinoma, metastatic", "shortest_name_length": 35}
{"curie": "UMLS:C1332279", "names": ["Anaplastic Brainstem Astrocytoma", "Anaplastic Brain Stem Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anaplastic Brain Stem Astrocytoma", "shortest_name_length": 32}
{"curie": "MONDO:0044648", "names": ["kyphoscoliosis-lateral tongue atrophy-HSP syndrome", "kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome", "shortest_name_length": 50}
{"curie": "MONDO:0006863", "names": ["myxosarcoma", "Myxosarcoma", "Myxosarcomas", "myxosarcoma, malignant", "Myxosarcoma (disorder)", "MYXOSARCOMA, MALIGNANT", "myxosarcoma (diagnosis)", "Myxosarcoma (morphologic abnormality)", "myxosarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myxosarcoma", "shortest_name_length": 11}
{"curie": "MONDO:0003553", "names": ["ampulla of vater adenosquamous carcinoma", "Ampulla of Vater Adenosquamous Carcinoma", "ampulla of Vater adenosquamous carcinoma", "hepatopancreatic ampulla adenosquamous carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ampulla of vater adenosquamous carcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0019328", "names": ["Cavernous lymphangioma", "Cavernous Lymphangioma", "cavernous lymphangioma", "cavernous; lymphangioma", "LYMPHANGIOMA, CAVERNOUS", "Lymphangioma, Cavernous", "lymphangioma; cavernous", "Cavernous Lymphangiomas", "macrocystic lymphangioma", "Macrocystic lymphangioma", "Lymphangiomas, Cavernous", "Cavernous lymphatic malformation", "cavernous lymphatic malformation", "Cavernous lymphangioma (disorder)", "macrocystic lymphatic malformation", "Macrocystic lymphatic malformation", "macrocystic lymphatic malformation (diagnosis)", "Cavernous lymphangioma (morphologic abnormality)", "disorder of lymphatic vessel lymphatic malformation macrocystic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macrocystic lymphatic malformation", "shortest_name_length": 22}
{"curie": "MONDO:0012502", "names": ["NFTC", "Normocalcemic tumoral calcinosis", "Normocalcaemic tumoural calcinosis", "CALCINOSIS, TUMORAL, WITH NORMOPHOSPHATEMIA", "calcinosis, tumoral, with Normophosphatemia", "Calcinosis, Tumoral, With Normophosphatemia", "Familial normophosphatemic tumoral calcinosis", "normophosphatemic familial tumoral calcinosis", "familial normophosphatemic tumoral calcinosis", "tumoral calcinosis, normophosphatemic, familial", "Tumoral Calcinosis, Normophosphatemic, Familial", "Familial normophosphataemic tumoural calcinosis", "TUMORAL CALCINOSIS, NORMOPHOSPHATEMIC, FAMILIAL", "tumoral calcinosis, familial, normophosphatemic", "Familial normophosphatemic tumoral calcinosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "normophosphatemic familial tumoral calcinosis", "shortest_name_length": 4}
{"curie": "UMLS:C4054382", "names": ["Nephrotic Syndrome - ITGA3 Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - ITGA3 Associated", "shortest_name_length": 37}
{"curie": "UMLS:C0560621", "names": ["Gum injury", "wound; gum", "gum; wound", "gum; injury", "injury; gum", "Gingival injury", "gingiva; injury", "injuries of gum", "Gingival Injury", "injury; gingiva", "mouth injury gum", "Gum injury (disorder)", "Gum injury (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gum injury", "shortest_name_length": 10}
{"curie": "UMLS:C5418922", "names": ["Metastatic Glioblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Glioblastoma", "shortest_name_length": 23}
{"curie": "UMLS:C0008628", "names": ["Partial Monosomy", "partial monosomy", "chromosome deletion", "deletion chromosome", "Chromosome Deletion", "Chromosomal Deletion", "deletion; chromosome", "chromosome deletions", "Deletion, Chromosome", "Chromosomal deletion", "chromosomal deletion", "Deletions, Chromosome", "Deletion (Chromosome)", "Chromosomal deletion NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chromosome Deletion", "shortest_name_length": 16}
{"curie": "MONDO:0012031", "names": ["BDPLT10", "CD36 DEFICIENCY", "CD36 deficiency", "CD36 Deficiency", "platelet glycoprotein 4 deficiency", "platelet-type bleeding disorder 10", "Platelet Glycoprotein IV Deficiency", "platelet glycoprotein IV deficiency", "PLATELET GLYCOPROTEIN IV DEFICIENCY", "bleeding disorder, Platelet-type, 10", "BLEEDING DISORDER, PLATELET-TYPE, 10", "CD36 inherited bleeding disorder, platelet-type", "inherited bleeding disorder, platelet-type caused by mutation in CD36"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "platelet-type bleeding disorder 10", "shortest_name_length": 7}
{"curie": "MONDO:0020597", "names": ["Fordyce Angiokeratoma", "scrotal angiokeratoma", "Scrotal Angiokeratoma", "scrotum angiokeratoma", "fordyce angiokeratoma", "angiokeratoma of scrotum", "Angiokeratoma of Fordyce", "angiokeratoma of fordyce", "Angiokeratoma of Scrotum", "Angiokeratoma of the Scrotum", "angiokeratoma of the scrotum", "Scrotal Fordyce-Type Angiokeratoma", "scrotal fordyce-type angiokeratoma", "fordyce-type angiokeratoma of scrotum", "Fordyce-Type Angiokeratoma of Scrotum", "Fordyce-Type Angiokeratoma of the Scrotum", "fordyce-type angiokeratoma of the scrotum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angiokeratoma of scrotum", "shortest_name_length": 21}
{"curie": "MONDO:0014184", "names": ["SLI5", "language impairment", "SPECIFIC LANGUAGE IMPAIRMENT 5", "specific language impairment 5", "specific language impairment type 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "specific language impairment 5", "shortest_name_length": 4}
{"curie": "UMLS:C5670997", "names": ["Refractory Vulvar Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Vulvar Squamous Cell Carcinoma", "shortest_name_length": 41}
{"curie": "UMLS:C0544618", "names": ["orthostatic hypertension", "Orthostatic hypertension", "hypertension orthostatic", "Hypertension, orthostatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Orthostatic hypertension", "shortest_name_length": 24}
{"curie": "MONDO:0002559", "names": ["plexiform neurinoma", "Plexiform Neurinoma", "Plexiform Schwannoma", "plexiform schwannoma", "Plexiform schwannoma", "Plexiform Neurilemmoma", "plexiform neurilemmoma", "Plexiform neurilemmoma", "Plexiform schwannoma (disorder)", "plexiform schwannoma (morphologic abnormality)", "Plexiform schwannoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "plexiform schwannoma", "shortest_name_length": 19}
{"curie": "MONDO:0011149", "names": ["premature aging Okamoto type", "Premature Aging Syndrome, Okamoto Type", "premature aging syndrome, Okamoto type", "PREMATURE AGING SYNDROME, OKAMOTO TYPE", "premature aging syndrome with osteosarcoma cataracts diabetes osteoporosis erythroid macrocytosis severe developmental delay"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "premature aging syndrome, Okamoto type", "shortest_name_length": 28}
{"curie": "MONDO:0002233", "names": ["Enamel caries", "enamel caries", "caries; enamel", "Caries, enamel", "enamel; caries", "caries of enamel", "Enamel caries, NOS", "Simple dental caries", "simple dental cavity", "Simple dental cavity", "enamel dental caries", "primary dental caries", "Dental caries, simple", "Dental cavity, simple", "Primary dental caries", "dental caries of enamel", "Caries limited to enamel", "Enamel caries (disorder)", "caries of enamel (diagnosis)", "Dental caries limited to enamel", "dental caries limited to enamel", "Dental caries confined to enamel", "Primary dental caries (disorder)", "primary dental caries (diagnosis)", "Cavitated lesion limited to enamel"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "enamel caries", "shortest_name_length": 13}
{"curie": "MONDO:0017267", "names": ["SICI", "SHCB", "Self-healing collodion baby", "self-healing collodion baby", "Self-Healing Collodion Baby", "COLLODION BABY, SELF-HEALING", "self-improving collodion baby", "Self-improving collodion baby", "self-improving congenital ichthyosis", "Self-improving congenital ichthyosis", "Self-healing collodion baby (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "self-healing collodion baby", "shortest_name_length": 4}
{"curie": "MONDO:0004019", "names": ["Oxyphilic Endometrial Endometrioid Adenocarcinoma", "oxyphilic endometrial endometrioid adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oxyphilic endometrial endometrioid adenocarcinoma", "shortest_name_length": 49}
{"curie": "MONDO:0004141", "names": ["melanomatosis", "Melanomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melanomatosis", "shortest_name_length": 13}
{"curie": "UMLS:C4687664", "names": ["Refractory Chemotherapy-Induced Nausea and Vomiting"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Chemotherapy-Induced Nausea and Vomiting", "shortest_name_length": 51}
{"curie": "MONDO:0016113", "names": ["SBMA", "kennedy syndrome", "syndrome kennedy", "Kennedy syndrome", "kennedys syndrome", "Bulbospinal neuronopathy", "bulbospinal neuronopathy", "Bulbospinal Neuronopathy", "Neuronopathy, Bulbospinal", "Bulbospinal Neuronopathies", "Neuronopathies, Bulbospinal", "bulbospinal muscular atrophy", "X-linked bulbospinal atrophy", "Bulbospinal muscular atrophy", "spinal-bulbar muscular atrophy", "spinal and bulbal muscular atrophy", "Bulbospinal neuronopathy (disorder)", "bulbospinal neuronopathy (diagnosis)", "congenital malformations nervous system bulbospinal neuronopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bulbospinal muscular atrophy", "shortest_name_length": 4}
{"curie": "MONDO:0018635", "names": ["idiopathic phalangeal acroosteolysis", "idiopathic phalangeal acro-osteolysis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic phalangeal acro-osteolysis", "shortest_name_length": 36}
{"curie": "MONDO:0017480", "names": ["amelia of lower limb, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amelia of lower limb, unilateral", "shortest_name_length": 32}
{"curie": "UMLS:C4055377", "names": ["Bladder Sphincter Dysfunction", "Detrusor Sphincter Dysynergia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder Sphincter Dysfunction", "shortest_name_length": 29}
{"curie": "UMLS:C3873513", "names": ["Invasive listeriosis", "Invasive Listeriosis", "Invasive listeriosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Invasive listeriosis", "shortest_name_length": 20}
{"curie": "UMLS:C5420197", "names": ["Laryngeal Pleomorphic Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laryngeal Pleomorphic Adenoma", "shortest_name_length": 29}
{"curie": "UMLS:C5204605", "names": ["CALFAN Syndrome", "Cholestasis, Acute Liver Failure, and Neurodegeneration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CALFAN Syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0024663", "names": ["primary skin meningioma", "Primary Skin Meningioma", "Primary Meningioma of Skin", "primary meningioma of skin", "Primary Cutaneous Meningioma", "primary cutaneous meningioma", "Primary Meningioma of the Skin", "primary meningioma of the skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary skin meningioma", "shortest_name_length": 23}
{"curie": "UMLS:C3897942", "names": ["Peritoneal Dialysis Catheter-Associated Peritonitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peritoneal Dialysis Catheter-Associated Peritonitis", "shortest_name_length": 51}
{"curie": "MONDO:0005826", "names": ["Oil pneumonitis", "Pneumonia lipid", "oil pneumonitis", "Lipid pneumonia", "Lipid Pneumonia", "lipid pneumonia", "pneumonia lipid", "LIPID PNEUMONIA", "lipoid pneumonia", "Pneumonia, Lipid", "Pneumonia lipoid", "LIPOID PNEUMONIA", "Lipid Pneumonias", "Lipoid pneumonia", "Lipoid Pneumonia", "Pneumonia, lipid", "pneumonia; lipids", "Pneumonia, lipoid", "lipids; pneumonia", "oils; pneumonitis", "Lipoid Pneumonias", "Lipid pneumonitis", "lipid pneumonitis", "lipoidpneumonitis", "Pneumonia, Lipoid", "pneumonitis; oils", "Lipoid pneumonitis", "lipoid pneumonitis", "Lipid pneumonia NOS", "cholesterol pneumonia", "Oil aspiration pneumonia", "Exogenous Lipid Pneumonia", "Exogenous lipoid pneumonia", "Pneumonia, Exogenous Lipid", "exogenous lipoid pneumonia", "Exogenous Lipid Pneumonias", "Lipid Pneumonia, Exogenous", "Exogenous Lipoid Pneumonia", "lipoid pneumonia exogenous", "pneumonia; aspiration, oils", "Lipoid Pneumonia, Exogenous", "Pneumonia, Exogenous Lipoid", "Exogenous Lipoid Pneumonias", "lipoid pneumonia (diagnosis)", "Lipoid interstitial pneumonia", "Lipoid pneumonitis (disorder)", "LIP - Lipoid interstitial pneumonia", "Pneumonitis due to inhalation of oils", "Exogenous lipoid pneumonia (disorder)", "Exogenous lipoid pneumonia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lipid pneumonia", "shortest_name_length": 15}
{"curie": "MONDO:0035666", "names": ["acute transverse myelitis with anti-MOG antibodies", "Acute transverse myelitis with anti-myelin oligodendrocyte glycoprotein antibodies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute transverse myelitis with anti-MOG antibodies", "shortest_name_length": 50}
{"curie": "MONDO:0024675", "names": ["adult nephroblastoma", "Adult Renal Wilms Tumor", "adult renal Wilms tumor", "Adult Renal Adenosarcoma", "adult renal adenosarcoma", "adult renal Wilms' tumor", "Adult Kidney Wilms Tumor", "adult kidney Wilms tumor", "Adult Renal Wilms' Tumor", "adult kidney adenosarcoma", "Adult Kidney Adenosarcoma", "Adult Kidney Nephroblastoma", "adenosarcoma of adult kidney", "kidney Wilms tumor of adults", "Adenosarcoma of Adult Kidney", "adenosarcoma of the adult kidney", "Adenosarcoma of the Adult Kidney"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult kidney Wilms tumor", "shortest_name_length": 20}
{"curie": "UMLS:C1335897", "names": ["Salivary Gland Cystadenocarcinoma", "cystadenocarcinoma of salivary gland", "Cystadenocarcinoma of Salivary Gland", "Cystadenocarcinoma of the Salivary Gland", "cystadenocarcinoma of salivary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cystadenocarcinoma of salivary gland", "shortest_name_length": 33}
{"curie": "MONDO:0012233", "names": ["LFS2", "Li-Fraumeni syndrome 2", "LI-FRAUMENI SYNDROME 2", "Li-Fraumeni Syndrome 2", "Li-Fraumeni syndrome LFS2", "Li-Fraumeni-Like Syndrome", "CHEK2 Li-Fraumeni syndrome", "Li-Fraumeni syndrome type 2", "Li-Fraumeni syndrome LFS2 (diagnosis)", "CHEK2-Associated Li-Fraumeni Syndrome", "Li-Fraumeni Syndrome, CHEK2-Associated", "CHEK2-Associated Cancer Predisposition", "CHEK2-Associated Li-Fraumeni-Like Syndrome", "Li-Fraumeni syndrome caused by mutation in CHEK2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Li-Fraumeni syndrome 2", "shortest_name_length": 4}
{"curie": "UMLS:C1275239", "names": ["Dermatomyofibroma", "Dermatomyofibroma (disorder)", "Plaque-Like Dermal Fibromatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dermatomyofibroma", "shortest_name_length": 17}
{"curie": "MONDO:0014472", "names": ["AIFEC", "NLRC4-related MAS", "NLRC4-related macrophage activation syndrome", "autoinflammation with infantile enterocolitis", "AUTOINFLAMMATION with infantile enterocolitis", "Autoinflammation with infantile enterocolitis", "AUTOINFLAMMATION WITH INFANTILE ENTEROCOLITIS", "NLRC4-related autoinflammatory syndrome with MAS", "NLRC4-related infantile enterocolitis-autoinflammatory syndrome", "Periodic fever-infantile enterocolitis-autoinflammatory syndrome", "periodic fever-infantile enterocolitis-autoinflammatory syndrome", "NLRC4-related infantile enterocolitis, autoinflammatory syndrome", "Periodic fever, infantile enterocolitis, autoinflammatory syndrome", "NLRC4-related autoinflammatory syndrome with macrophage activation syndrome", "Periodic fever, infantile enterocolitis, autoinflammatory syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "periodic fever-infantile enterocolitis-autoinflammatory syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C1719672", "names": ["severe sepsis", "Severe Sepsis", "Severe sepsis", "Sepsis, Severe", "Severe sepsis NOS", "severe sepsis (diagnosis)", "Sepsis with Organ Dysfunction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Severe Sepsis", "shortest_name_length": 13}
{"curie": "MONDO:0018353", "names": ["refractory CD", "refractory sprue", "type I refractory sprue", "type II refractory sprue", "intractable celiac sprue", "refractory celiac disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "refractory celiac disease", "shortest_name_length": 13}
{"curie": "UMLS:C1332060", "names": ["AIDS-Related Retinopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Retinopathy", "shortest_name_length": 24}
{"curie": "MONDO:0014491", "names": ["IMD37", "immunodeficiency 37", "IMMUNODEFICIENCY 37", "immunodeficiency type 37", "BCL10 primary immunodeficiency disease", "combined immunodeficiency due to BCL10 deficiency", "primary immunodeficiency disease caused by mutation in BCL10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 37", "shortest_name_length": 5}
{"curie": "MONDO:0000782", "names": ["Indian plum allergy", "Ziziphus mauritiana fruit allergy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Indian plum allergy", "shortest_name_length": 19}
{"curie": "UMLS:C5420334", "names": ["Refractory Acute Biphenotypic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Acute Biphenotypic Leukemia", "shortest_name_length": 38}
{"curie": "UMLS:C1399315", "names": ["Subarachnoid hematoma", "Subarachnoid Hematoma", "subarachnoid; hematoma", "hematoma; subarachnoid", "Subarachnoid haematoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subarachnoid hematoma", "shortest_name_length": 21}
{"curie": "MONDO:0006143", "names": ["CESC", "Squamous cervical cancer", "squamous cervical cancer", "cancer cell cervix squamous", "Carcinoma;cervix;squam cell", "cancer cells cervix squamous", "cervical epidermoid carcinoma", "squamous cell cervical cancer", "cervical cancer squamous cell", "cervical squamous cell cancer", "CERVICAL CANCER SQUAMOUS CELL", "Cervical Squamous Cell Cancer", "cervix squamous cell carcinoma", "carcinoma cell cervix squamous", "Cervix Squamous Cell Carcinoma", "squamous cell carcinoma cervix", "Cervical squamous cell carcinoma", "squamous cell carcinoma cervical", "cervical squamous cell carcinoma", "Cervical Squamous Cell Carcinoma", "squamous cell carcinoma of cervix", "Squamous cell carcinoma of cervix", "Squamous Cell Carcinoma of Cervix", "squamous cell cancer of the cervix", "epidermoid carcinoma of the cervix", "cancer of the cervix, squamous cell", "cervix uteri squamous cell carcinoma", "sqamous cell carcinoma of the cervix", "Cervix Uteri Squamous Cell Carcinoma", "Squamous Cell Carcinoma of the Cervix", "squamous cell carcinoma of the cervix", "Squamous cell carcinoma of the cervix", "Uterine Cervix Squamous Cell Carcinoma", "uterine cervix squamous cell carcinoma", "cervix cancer, squamous cell carcinoma", "carcinoma of the cervix, squamous cell", "squamous cell carcinoma of cervix uteri", "Squamous Cell Carcinoma of Cervix Uteri", "cervical cancer, squamous cell carcinoma", "squamous cell carcinoma of uterine cervix", "Squamous Cell Carcinoma of Uterine Cervix", "squamous cell carcinoma of the Cervix Uteri", "Squamous cell carcinoma of the cervix uteri", "squamous cell carcinoma of the cervix uteri", "Squamous Cell Carcinoma of the Cervix Uteri", "Squamous cell carcinoma of cervix (disorder)", "squamous cell carcinoma of the uterine cervix", "Squamous Cell Carcinoma of the Uterine Cervix", "squamous cell carcinoma of cervix (diagnosis)", "uterine cervix cancer, squamous cell carcinoma", "uterine cervical cancer, squamous cell carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical squamous cell carcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0021115", "names": ["Luminal B", "Luminal B Breast Cancer", "Luminal B breast cancer", "luminal breast carcinoma B", "Luminal B breast carcinoma", "luminal B breast carcinoma", "Luminal B Breast Carcinoma", "Luminal B subtype of breast carcinoma", "Luminal B Subtype of Breast Carcinoma", "Luminal B Estrogen Receptor Positive Subtype of Breast Carcinoma", "Luminal B estrogen receptor positive subtype of breast carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "luminal B breast carcinoma", "shortest_name_length": 9}
{"curie": "MONDO:0100259", "names": ["PEX1 related Zellweger spectrum disorder", "peroxisome biogenesis disorder due to PEX1 defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder due to PEX1 defect", "shortest_name_length": 40}
{"curie": "MONDO:0033572", "names": ["IDDEBF", "intellectual developmental disorder with epilepsy, behavioral abnormalities, and coarse facies", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH EPILEPSY, BEHAVIORAL ABNORMALITIES, AND COARSE FACIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder with epilepsy, behavioral abnormalities, and coarse facies", "shortest_name_length": 6}
{"curie": "MONDO:0003064", "names": ["columnar cell papilloma", "cylindrical cell papilloma", "Inverted Transitional Papilloma", "inverted transitional papilloma", "transitional papilloma, inverted", "Inverted transitional cell papilloma", "Inverted Transitional Cell Papilloma", "inverted transitional cell papilloma", "Transitional cell papilloma, inverted", "Transitional papilloma, inverted, NOS", "Transitional cell papilloma, inverted, NOS", "Transitional cell papilloma, inverted type", "Inverted transitional cell papilloma of uncertain behavior", "Inverted transitional cell papilloma of uncertain behaviour", "Inverted transitional papilloma uncertain whether benign or malignant", "Transitional papilloma, inverted, uncertain whether benign or malignant", "Inverted transitional cell papilloma uncertain whether benign or malignant", "Transitional cell papilloma, inverted, uncertain whether benign or malignant", "Inverted transitional cell papilloma of uncertain behavior (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inverted transitional cell papilloma", "shortest_name_length": 23}
{"curie": "UMLS:C0264220", "names": ["Chronic respiratory disease", "chronic disease respiratory", "respiratory disease chronic", "chronic respiratory disease", "chronic diseases respiratory", "Chronic respiratory disease NOS", "Chronic respiratory disease, NOS", "Respiratory disease (chronic) NOS", "Chronic respiratory system disease", "Chronic disease of respiratory system", "Chronic disease of respiratory system (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic disease of respiratory system", "shortest_name_length": 27}
{"curie": "MONDO:0011256", "names": ["EMPHYSEMA, CONGENITAL, WITH DEAFNESS, PENOSCROTAL WEB, AND MENTAL RETARDATION", "emphysema, congenital, with deafness, penoscrotal web, and mental retardation", "Emphysema, Congenital, With Deafness, Penoscrotal Web, And Mental Retardation", "emphysema, congenital, with deafness, penoscrotal web, and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "emphysema, congenital, with deafness, penoscrotal web, and intellectual disability", "shortest_name_length": 77}
{"curie": "UMLS:C5206724", "names": ["Resectable Osteosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Osteosarcoma", "shortest_name_length": 23}
{"curie": "UMLS:C4553871", "names": ["stage 0a urethral cancer", "Stage 0a Urethral Cancer", "Stage 0a Urethral Cancer AJCC v8", "stage 0a urethral cancer AJCC v8", "stage 0a urethral carcinoma AJCC v8", "Stage 0a Urethral Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0a Urethral Cancer AJCC v8", "shortest_name_length": 24}
{"curie": "MONDO:0011731", "names": ["GM", "GGM", "SGLT1 deficiency", "Carbohydrate Intolerance", "MONOSACCHARIDE MALABSORPTION", "Monosaccharide Malabsorption", "monosaccharide malabsorption", "malabsorption; monosaccharide", "monosaccharide; malabsorption", "glucose-galactose malabsorption", "glucose/galactose malabsorption", "Glucose Galactose Malabsorption", "Glucose-Galactose Malabsorption", "Glucose-galactose malabsorption", "GLUCOSE/GALACTOSE MALABSORPTION", "glucose galactose malabsorption", "Complex Carbohydrate Intolerance", "Complex carbohydrate intolerance", "Monosaccharide malabsorption syndrome", "Congenital monosaccharide malabsorption", "Congenital glucose-galactose intolerance", "Glucose-galactose malabsorption (disorder)", "Congenital glucose-galactose malabsorption", "glucose galactose malabsorption deficiency", "congenital glucose-galactose malabsorption", "carbohydrate intolerance of glucose galactose", "Congenital glucose-galactose malabsorption syndrome", "Congenital glucose-galactose malabsorption (disorder)", "congenital glucose-galactose malabsorption (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glucose-galactose malabsorption", "shortest_name_length": 2}
{"curie": "UMLS:C1706705", "names": ["Active Peptic Ulcer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Active Peptic Ulcer", "shortest_name_length": 19}
{"curie": "UMLS:C1706830", "names": ["Appendix Lipoma", "Lipoma of appendix", "Lipoma of appendix (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lipoma of appendix", "shortest_name_length": 15}
{"curie": "MONDO:0011485", "names": ["NNCI", "ARCI5", "LI3, formerly", "LI3, FORMERLY", "ichthyosis lamellar 3", "Ichthyosis lamellar 3", "Ichthyosis congenita 3", "ichthyosis congenita 3", "Ichthyosis, Lamellar, 3", "ICHTHYOSIS, LAMELLAR, 3", "ichthyosis, lamellar, 3", "Ichthyosis Congenita III", "ICHTHYOSIS CONGENITA III", "ichthyosis congenita III", "type 3 lamellar ichthyosis", "Type 3 lamellar ichthyosis", "lamellar ichthyosis, type 3", "Lamellar ichthyosis, type 3", "ichthyosis, lamellar, 3, formerly", "ICHTHYOSIS, LAMELLAR, 3, FORMERLY", "autosomal recessive congenital ichthyosis 5", "ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 5", "ichthyosis, congenital, autosomal recessive 5", "autosomal recessive congenital ichthyosis type 5", "ichthyosis, congenital, autosomal recessive type 5", "autosomal recessive congenital nonlamellar and nonerythrodermic ichthyosis", "ichthyosis, NONLAMELLAR and NONERYTHRODERMIC, congenital, autosomal recessive", "ichthyosis, Nonlamellar and Nonerythrodermic, congenital, autosomal recessive", "ICHTHYOSIS, NONLAMELLAR AND NONERYTHRODERMIC, CONGENITAL, AUTOSOMAL RECESSIVE", "Ichthyosis, Nonlamellar and Nonerythrodermic, Congenital, Autosomal Recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive congenital ichthyosis 5", "shortest_name_length": 4}
{"curie": "MONDO:0017843", "names": ["Cystic lung lesion", "sequestration lung", "lung sequestration", "LUNG, SEQUESTRATION", "Sequestration of lung", "sequestration of lung", "Pulmonary sequestration", "Pulmonary Sequestration", "sequestration pulmonary", "pulmonary sequestration", "Sequestration, Pulmonary", "pulmonary sequestrations", "Pulmonary Sequestrations", "Sequestrations, Pulmonary", "bronchopulmonary sequestration", "Bronchopulmonary Sequestration", "BRONCHOPULMONARY SEQUESTRATION", "Bronchopulmonary sequestration", "Sequestration, Bronchopulmonary", "Bronchopulmonary Sequestrations", "Sequestrations, Bronchopulmonary", "congenital sequestration of lung", "Congenital Sequestration of Lung", "Congenital sequestration of lung", "Congenital pulmonary sequestration", "congenital pulmonary sequestration", "congenital bronchopulmonary sequestration", "Congenital bronchopulmonary sequestration", "bronchopulmonary sequestration (diagnosis)", "Sequestered Lobe (Pulmonary Sequestration)", "sequestered lobe (pulmonary sequestration)", "Congenital sequestration of lung (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital pulmonary sequestration", "shortest_name_length": 18}
{"curie": "MONDO:0009300", "names": ["PRLTS1", "PERRAULT SYNDROME 1", "Perrault syndrome 1", "Perrault syndrome type 1", "HSD17B4 Perrault syndrome", "gonadal dysgenesis, 20 type, with deafness", "ovarian dysgenesis with sensorineural deafness", "Perrault syndrome caused by mutation in HSD17B4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perrault syndrome 1", "shortest_name_length": 6}
{"curie": "MONDO:0012889", "names": ["SS3", "SARCOIDOSIS, SUSCEPTIBILITY TO, 3", "sarcoidosis, susceptibility to, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sarcoidosis, susceptibility to, 3", "shortest_name_length": 3}
{"curie": "MONDO:0044313", "names": ["MRT60", "mental retardation, autosomal recessive 60", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 60", "intellectual disability, autosomal recessive 60", "autosomal recessive intellectual developmental disorder 60", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 60"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 60", "shortest_name_length": 5}
{"curie": "MONDO:0004701", "names": ["uterus polyp", "polyp uterus", "Uterus Polyp", "polyp uterine", "uterus; polyp", "polyp; uterus", "Uterine polyp", "uterine polyp", "polyp, uterus", "UTERINE POLYP", "Uterine Polyp", "polyps uterus", "polyps uterine", "polyp of uterus", "Polyp of Uterus", "Polyp, uterus NOS", "Uterine polyp NOS", "Intrauterine polyp", "intrauterine polyp", "polyp of the uterus", "Polyp of the Uterus", "polyp of the Uterus", "Polyp of uterus NOS", "intrauterine polyps", "polyp; corpus uteri", "corpus uteri; polyp", "polyp of endometrium", "polyp of Endometrium", "Polyp of corpus uteri", "polyp of corpus uteri", "Polyp of body of uterus", "endometrial/uterine polyp", "Polyp of corpus uteri (disorder)", "polyp of corpus uteri (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine polyp", "shortest_name_length": 12}
{"curie": "MONDO:0020655", "names": ["juvenile ankylosing spondylitis", "Juvenile ankylosing spondylitis", "juvenile ankylosing; spondylitis", "spondylitis; juvenile ankylosing", "spondylitis; ankylosing, juvenile", "AS - Juvenile ankylosing spondylitis", "ankylopoietica; spondylitis, juvenile", "Juvenile ankylosing spondylitis (disorder)", "juvenile ankylosing spondylitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile ankylosing spondylitis", "shortest_name_length": 31}
{"curie": "MONDO:0008431", "names": ["SCFE", "SUFE", "Adolescent Coxa Vara", "COXA VARA, ADOLESCENT", "Coxa Vara, Adolescent", "Adolescent Coxa Varas", "COXA VARA, EPIPHYSEAL", "Slipped femoral epiphysis", "Slipped;femoral epiphysis", "Epiphysiolysis of the hip", "slipped femoral epiphysis", "FEMUR, EPIPHYSIS, SLIPPING", "Femoral head epiphysiolysis", "EPIPHYSIS, FEMUR, SEPARATION", "Epiphysiolysis Capitis Femoris", "Slipped femoral epiphysis, NOS", "epiphysiolysis capitis femoris", "EPIPHYSIOLYSIS CAPITIS FEMORIS", "epiphysis femoral slipped upper", "Slipped upper femoral epiphysis", "slipped upper femoral epiphysis", "Proximal femoral epiphysiolysis", "EPIPHYSIOLYSIS, PROXIMAL FEMORAL", "Slipped Capital Femoral Epiphysis", "Slipped Femoral Capital Epiphyses", "Slipped capital femoral epiphyses", "SLIPPED FEMORAL CAPITAL EPIPHYSES", "slipped femoral capital epiphyses", "Slipped femoral capital epiphysis", "SLIPPED CAPITAL FEMORAL EPIPHYSIS", "slipped femoral capital epiphysis", "Slipped Capital Femoral Epiphyses", "Epiphysiolysis of the upper femur", "capital epiphysis femoral slipped", "Slipped capital femoral epiphysis", "Slipped upper femoral epiphysis NOS", "Slipped upper femoral epiphysis, NOS", "SUFE - Slipped upper femoral epiphysis", "Slipped upper femoral epiphysis (SUFE)", "Slipped end part of innermost thighbone", "Slipped upper femoral epiphysis (disorder)", "slipped upper femoral epiphysis (diagnosis)", "Nontraumatic slipped upper femoral epiphysis", "Non-traumatic slipped upper femoral epiphysis", "Slipped upper femoral epiphysis (nontraumatic)", "Nontraumatic slipped upper femoral epiphysis, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "slipped femoral capital epiphyses", "shortest_name_length": 4}
{"curie": "UMLS:C5419749", "names": ["Recurrent Acute Leukemia of Ambiguous Lineage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Acute Leukemia of Ambiguous Lineage", "shortest_name_length": 45}
{"curie": "UMLS:C4744584", "names": ["Frontal Lobe Anaplastic Oligodendroglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Frontal Lobe Anaplastic Oligodendroglioma", "shortest_name_length": 41}
{"curie": "MONDO:0042484", "names": ["SPOROTRICHOSIS SYSTEMIC", "Generalized sporotrichosis", "sporotrichosis; generalized", "Disseminated sporotrichosis", "disseminated sporotrichosis", "generalized; sporotrichosis", "sporotrichosis; disseminated", "disseminated; sporotrichosis", "Disseminated sporotrichosis (disorder)", "disseminated sporotrichosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disseminated sporotrichosis", "shortest_name_length": 23}
{"curie": "MONDO:0032821", "names": ["MYOSCO", "congenital myopathy 19", "MYOPATHY, CONGENITAL, PROGRESSIVE, WITH SCOLIOSIS", "myopathy, congenital, progressive, with scoliosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy, congenital, progressive, with scoliosis", "shortest_name_length": 6}
{"curie": "MONDO:0015565", "names": ["Cap polyposis", "cap polyposis", "Cap polyposis (disorder)", "cap polyposis (diagnosis)", "Polypoid prolapsing folds", "polypoid prolapsing folds", "Cap inflammatory polyposis", "Eroded polypoid hyperplasia", "eroded polypoid hyperplasia", "Inflammatory myoglandular polyps", "inflammatory myoglandular polyps"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cap polyposis", "shortest_name_length": 13}
{"curie": "MONDO:0014517", "names": ["GEFS+9", "GEFSP9", "GEFS+, TYPE 9", "Gefs+, type 9", "generalised epilepsy with febrile seizures plus 9", "generalized epilepsy with febrile seizures plus 9", "STX1B generalized epilepsy with febrile seizures plus", "STX1b generalized epilepsy with febrile seizures plus", "generalised epilepsy with febrile seizures plus type 9", "generalized epilepsy with febrile seizures plus type 9", "GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 9", "generalized epilepsy with febrile seizures plus, type 9", "generalized epilepsy with febrile seizures plus caused by mutation in STX1b", "generalized epilepsy with febrile seizures plus caused by mutation in STX1B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "generalized epilepsy with febrile seizures plus, type 9", "shortest_name_length": 6}
{"curie": "MONDO:0011486", "names": ["MDC1B", "CMD1B", "congenital muscular dystrophy 1B", "MUSCULAR DYSTROPHY, CONGENITAL, 1B", "Muscular Dystrophy, Congenital, 1B", "muscular dystrophy, congenital, 1B", "congenital muscular dystrophy type 1B", "Congenital muscular dystrophy type 1B", "Congenital muscular dystrophy type 1B (disorder)", "Congenital muscular dystrophy type 1B (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital muscular dystrophy 1B", "shortest_name_length": 5}
{"curie": "MONDO:0000293", "names": ["Gid", "sturdy", "caenurosis", "Coenurosis", "coenurosis", "coenuriasis", "Coenuriases", "Coenuriasis", "Coenurosis (disorder)", "coenurosis (diagnosis)", "infection by tapeworm larva", "Infection by larvae of Multiceps", "infection by larvae of multiceps", "Infection by larvae of dog tapeworm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coenurosis", "shortest_name_length": 3}
{"curie": "MONDO:0007438", "names": ["dentin dysplasia sclerotic bones", "Dentin dysplasia sclerotic bones", "sclerotic bones with dentin dysplasia", "Sclerotic bones with dentin dysplasia", "DENTIN DYSPLASIA WITH SCLEROTIC BONES", "Dentin Dysplasia with Sclerotic Bones", "dentin dysplasia with sclerotic bones", "dentin dysplasia-sclerotic bones syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dentin dysplasia-sclerotic bones syndrome", "shortest_name_length": 32}
{"curie": "UMLS:C1112668", "names": ["Cardiac septal hypertrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiac septal hypertrophy", "shortest_name_length": 26}
{"curie": "UMLS:C1335713", "names": ["Relapsed Meningioma", "Recurrent Meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Meningioma", "shortest_name_length": 19}
{"curie": "MONDO:0018109", "names": ["fulminant viral hepatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fulminant viral hepatitis", "shortest_name_length": 25}
{"curie": "MONDO:0016473", "names": ["RTPS", "familial rhabdoid tumor", "Familial rhabdoid tumor", "Familial rhabdoid tumour", "hereditary rhabdoid tumor", "Rhabdoid Predisposition Syndrome", "rhabdoid predisposition syndrome", "Rhabdoid Tumor Predisposition Syndrome", "Rhabdoid tumor predisposition syndrome", "rhabdoid tumor predisposition syndrome", "Rhabdoid tumour predisposition syndrome", "Rhabdoid tumor predisposition syndrome (disorder)", "familial posterior fossa brain tumor syndrome of infancy", "Familial Posterior Fossa Brain Tumor Syndrome of Infancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial rhabdoid tumor", "shortest_name_length": 4}
{"curie": "MONDO:0011900", "names": ["DSAP2", "POROK4", "Porokeratosis, Disseminated Superficial Actinic 2", "porokeratosis 4, disseminated superficial actinic", "Porokeratosis, disseminated superficial actinic 2", "POROKERATOSIS, DISSEMINATED SUPERFICIAL ACTINIC, 2", "porokeratosis, disseminated superficial actinic, 2", "Porokeratosis, Disseminated Superficial Actinic, 2", "porokeratosis 4, disseminated superficial actinic type", "POROKERATOSIS 4, DISSEMINATED SUPERFICIAL ACTINIC TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "porokeratosis 4, disseminated superficial actinic type", "shortest_name_length": 5}
{"curie": "UMLS:C5555676", "names": ["Unresectable Malignant Thoracic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Malignant Thoracic Neoplasm", "shortest_name_length": 40}
{"curie": "MONDO:0002425", "names": ["Rectosigmoid colon cancer", "Malignant Rectosigmoid Tumor", "malignant rectosigmoid tumor", "rectosigmoid junction cancer", "malignant Rectosigmoid tumor", "cancer of rectosigmoid junction", "Malignant Rectosigmoid Neoplasm", "malignant rectosigmoid neoplasm", "Malignant neoplasm of rectosigmoid", "malignant neoplasm of rectosigmoid", "malignant rectosigmoid junction neoplasm", "Malignant tumor of rectosigmoid junction", "Malignant Tumor of Rectosigmoid Junction", "malignant tumor of rectosigmoid junction", "Malignant neoplasm of rectosigmoid colon", "Malignant tumour of rectosigmoid junction", "Malignant neoplasm of rectosigmoid (colon)", "Malignant Neoplasm of Rectosigmoid Junction", "Malignant neoplasm of rectosigmoid junction", "malignant neoplasm of rectosigmoid junction", "malignant tumor of the rectosigmoid junction", "Malignant Tumor of the Rectosigmoid Junction", "Malignant Neoplasm of the Rectosigmoid Junction", "malignant neoplasm of the rectosigmoid junction", "rectal neoplasm malignant rectosigmoid junction", "Malignant tumor of rectosigmoid junction (disorder)", "malignant neoplasm of rectosigmoid junction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rectosigmoid junction cancer", "shortest_name_length": 25}
{"curie": "UMLS:C2984532", "names": ["Stage I Gallbladder Cancer", "stage IA gallbladder cancer", "stage IB gallbladder cancer", "Stage I Gallbladder Cancer AJCC v6", "Gallbladder Cancer Stage I AJCC v6", "Stage I Gallbladder Carcinoma AJCC v6", "Gallbladder Carcinoma Stage I AJCC v6", "Stage I Carcinoma of Gallbladder AJCC v6", "Stage I Carcinoma of the Gallbladder AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Gallbladder Cancer AJCC v6", "shortest_name_length": 26}
{"curie": "MONDO:0012656", "names": ["LCCS3", "lethal congenital contracture syndrome 3", "LETHAL CONGENITAL CONTRACTURE SYNDROME 3", "lethal congenital contractural syndrome 3", "Lethal Congenital Contractural Syndrome 3", "LETHAL CONGENITAL CONTRACTURAL SYNDROME 3", "Lethal congenital contracture syndrome type 3", "lethal congenital contracture syndrome type 3", "PIP5K1C lethal congenital contracture syndrome", "Israeli Bedouin type B multiple contracture syndrome", "multiple contracture syndrome, Israeli Bedouin type B", "MULTIPLE CONTRACTURE SYNDROME, ISRAELI BEDOUIN TYPE B", "Multiple Contractural Syndrome, Israeli Bedouin Type B", "Lethal congenital contracture syndrome type 3 (disorder)", "lethal congenital contracture syndrome caused by mutation in PIP5K1C"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal congenital contracture syndrome 3", "shortest_name_length": 5}
{"curie": "UMLS:C0851946", "names": ["Peritoneal and Retroperitoneal Hemorrhage", "Peritoneal and retroperitoneal hemorrhages", "Peritoneal and retroperitoneal haemorrhages"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peritoneal and retroperitoneal haemorrhages", "shortest_name_length": 41}
{"curie": "UMLS:C4682627", "names": ["Stage IVB Ovarian Cancer", "Stage IVB Ovarian Cancer AJCC v8", "Stage IVB Ovarian Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Ovarian Cancer AJCC v8", "shortest_name_length": 24}
{"curie": "UMLS:C3828503", "names": ["Postpartum Uterine Inversion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postpartum Uterine Inversion", "shortest_name_length": 28}
{"curie": "MONDO:0005487", "names": ["Cyclic schizophrenia", "cyclic schizophrenia", "cyclic; schizophrenic", "Schizo-affective type", "schizophrenia; cyclic", "SCHIZOAFFECTIVE DISORDER", "schizoaffective disorder", "disorder schizoaffective", "Schizoaffective disorder", "Schizoaffective Disorder", "Schizoaffective Disorders", "Psychosis;schizoaffective", "Schizoaffective disorders", "SCHIZO AFFECTIVE DISORDER", "schizoaffective disorders", "affective disorder schizo", "Disorder, Schizoaffective", "Schizoaffective psychosis", "schizo affective disorder", "disorder; schizoaffective", "schizoaffective psychosis", "Disorders, Schizoaffective", "Schizo-affective psychosis", "psychosis; schizoaffective", "Schizophrenia schizoaffective", "Schizoaffective psychosis NOS", "Schizoaffective schizophrenia", "Schizoaffective disorder, NOS", "schizoaffective schizophrenia", "SCHIZO AFFECTIVE SCHIZOPHRENIA", "schizoaffective-type schizophrenia", "Schizoaffective disorder (disorder)", "Schizo-affective type schizophrenia", "Schizophrenia, schizo-affective type", "schizoaffective disorder (diagnosis)", "Schizoaffective disorder, unspecified", "SCHIZO AFFECTIVE DISORDER UNSPECIFIED", "Schizoaffective schizophrenia (disorder)", "schizoaffective schizophrenia (diagnosis)", "Schizophreniform psychosis, affective type", "psychosis; schizophreniform, affective type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schizoaffective disorder", "shortest_name_length": 20}
{"curie": "MONDO:0007976", "names": ["Mesomelic Dwarfism of Hypoplastic Tibia and Radius Type", "mesomelic dwarfism of hypoplastic tibia and radius type", "MESOMELIC DWARFISM OF HYPOPLASTIC TIBIA AND RADIUS TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mesomelic dwarfism of hypoplastic tibia and radius type", "shortest_name_length": 55}
{"curie": "UMLS:C0393675", "names": ["Childhood Benign Occipital Epilepsy", "Benign Occipital Epilepsy, Childhood", "Benign occipital epilepsy of childhood", "Childhood epilepsy with occipital paroxysms", "Childhood epilepsy with occipital paroxysms (disorder)", "BCEOP - Benign childhood epilepsy with occipital paroxysms"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Benign Occipital Epilepsy", "shortest_name_length": 35}
{"curie": "UMLS:C0521510", "names": ["Implant site reaction", "Implant site reaction NOS", "Implant site reaction, NOS", "Implant site reaction (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Implant site reaction", "shortest_name_length": 21}
{"curie": "UMLS:C1335913", "names": ["G1 Grade 1", "FNCLCC Sarcoma Grade 1", "Sarcoma FNCLCC Grade 1", "Sarcoma Differentiation Score 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FNCLCC Sarcoma Grade 1", "shortest_name_length": 10}
{"curie": "UMLS:C2894027", "names": ["post-traumatic osteoarthritis", "Post-traumatic osteoarthritis", "Post traumatic osteoarthritis", "osteoarthritis post-traumatic", "Post-traumatic osteoarthritis NOS", "Post traumatic osteoarthritis (disorder)", "post-traumatic osteoarthritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post traumatic osteoarthritis", "shortest_name_length": 29}
{"curie": "UMLS:C4727171", "names": ["Locally Advanced Chordoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Chordoma", "shortest_name_length": 25}
{"curie": "UMLS:C5205550", "names": ["Locally Advanced Lung Non-Small Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Lung Non-Small Cell Carcinoma", "shortest_name_length": 46}
{"curie": "MONDO:0017638", "names": ["MANGANISM", "Manganism", "manganism", "manganese poison", "Manganic pneumonia", "Manganese poisoning", "Manganese Poisoning", "MANGANESE POISONING", "manganese poisoning", "Manganic pneumonitis", "Poisoning, Manganese", "pneumonitis manganese", "Manganese pneumonitis", "manganese; pneumonitis", "manganese intoxication", "Poisoning by manganese", "pneumonitis; manganese", "Manganese intoxication", "Poisoning caused by manganese", "Manganese pneumonitis (disorder)", "Manganese Neurotoxicity Syndrome", "Syndrome, Manganese Neurotoxicity", "Manganese Neurotoxicity Syndromes", "Neurotoxicity Syndrome, Manganese", "Manganese pneumonitis (diagnosis)", "Syndromes, Manganese Neurotoxicity", "Neurotoxicity Syndromes, Manganese", "Nervous System Poisoning, Manganese", "poisoning by manganese and compounds", "poisoning by manganese and its compounds", "Poisoning caused by manganese (disorder)", "Nervous System Diseases, Manganese Induced", "Nervous System Diseases, Manganese-Induced", "poisoning by manganese and its compounds (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "manganese poisoning", "shortest_name_length": 9}
{"curie": "MONDO:0002750", "names": ["Bladder Colloid Adenocarcinoma", "bladder colloid adenocarcinoma", "Bladder Mucinous Adenocarcinoma", "bladder mucinous adenocarcinoma", "mucinous adenocarcinoma of bladder", "mucinous adenocarcinoma of bladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder colloid adenocarcinoma", "shortest_name_length": 30}
{"curie": "UMLS:C0752197", "names": ["Adult-Onset Dystonia", "Adult-Onset Dystonias", "DYSTONIA, ADULT-ONSET", "Adult Onset Dystonias", "Dystonia, Adult-Onset", "Dystonias, Adult-Onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult-Onset Dystonias", "shortest_name_length": 20}
{"curie": "MONDO:0009593", "names": ["SMDS", "SEDAGHATIAN CHONDRODYSPLASIA", "Lethal Metaphyseal Dysplasia", "Sedaghatian chondrodysplasia", "Sedaghatian Chondrodysplasia", "lethal metaphyseal dysplasia", "congenital lethal metaphyseal chondrodysplasia", "spondylometaphyseal dysplasia Sedaghatian type", "spondylometaphyseal dysplasia, Sedaghatian type", "METAPHYSEAL CHONDRODYSPLASIA, CONGENITAL LETHAL", "Spondylometaphyseal dysplasia, Sedaghatian type", "metaphyseal chondrodysplasia, congenital lethal", "Metaphyseal Chondrodysplasia, Congenital Lethal", "SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondylometaphyseal dysplasia, Sedaghatian type", "shortest_name_length": 4}
{"curie": "UMLS:C4763827", "names": ["Metanephric Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metanephric Tumor", "shortest_name_length": 17}
{"curie": "MONDO:0025129", "names": ["Swine erysipelas", "swine erysipelas", "Swine Erysipelas", "erysipelas, swine", "Diamond skin disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "swine erysipelas", "shortest_name_length": 16}
{"curie": "MONDO:0006989", "names": ["apical abscess", "Apical abscess", "abscess; apical", "alveolar abscess", "Alveolar abscess", "abscess; alveolar", "alveolar; abscess", "ABSCESS, ALVEOLAR", "Periapical abscess", "periapical abscess", "Periapical Abscess", "Abscess, Periapical", "periapical; abscess", "Periapical abscesses", "Periapical Abscesses", "dentoalveolar abscess", "Abscesses, Periapical", "abscess dentoalveolar", "Dentoalveolar Abscess", "Dentoalveolar abscess", "abscess; dentoalveolar", "dentoalveolar; abscess", "DENTO ALVEOLAR ABSCESS", "Apical Alveolar Abscess", "Alveolar Abscess, Apical", "Abscess, Apical Alveolar", "Apical Alveolar Abscesses", "Periapical dental abscess", "periapical dental abscess", "Periapical Dental Abscess", "Alveolar Abscesses, Apical", "Abscesses, Apical Alveolar", "periapical alveolar abscess", "Apical Dentoalveolar Abscess", "Dentoalveolar Abscess, Apical", "Abscess, Apical Dentoalveolar", "Periapical abscess (disorder)", "Tooth root periapical abscess", "periapical abscess (diagnosis)", "Apical Dentoalveolar Abscesses", "Dentoalveolar Abscesses, Apical", "Abscesses, Apical Dentoalveolar", "Suppurative apical periodontitis", "suppurative apical periodontitis", "dentoalveolar abscess (diagnosis)", "Periodontitis, Apical, Suppurative", "Suppurative Periapical Periodontitis", "suppurative periapical periodontitis", "Periapical Periodontitis, Suppurative", "Periodontitis, Suppurative Periapical", "Suppurative Periapical Periodontitides", "Periodontitides, Suppurative Periapical", "Periapical Periodontitides, Suppurative", "periapical alveolar abscess (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "suppurative periapical periodontitis", "shortest_name_length": 14}
{"curie": "MONDO:0017861", "names": ["anti freeze poisoning", "Anti-freeze poisoning", "anti-freeze poisoning", "ETHYLENE GLYCOL TOXICITY", "ethylene glycol toxicity", "ethylene glycol poisoning", "Ethylene glycol poisoning", "Antifreeze causing toxic effect", "Ethylene glycol poisoning (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ethylene glycol poisoning", "shortest_name_length": 21}
{"curie": "UMLS:C1516062", "names": ["Astler-Coller B2 Colon Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Astler-Coller B2 Colon Carcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C1335998", "names": ["Small Bowel Hodgkin's Disease", "Small Bowel Hodgkin's Lymphoma", "Small Intestine Hodgkin Lymphoma", "Hodgkin's Disease of Small Bowel", "Small Intestine Hodgkin's Disease", "Small Intestinal Hodgkin Lymphoma", "Hodgkin's Lymphoma of Small Bowel", "Small Intestine Hodgkin's Lymphoma", "Small Intestinal Hodgkin's Lymphoma", "Hodgkin's Disease of Small Intestine", "Hodgkin's Disease of the Small Bowel", "Hodgkin's Lymphoma of Small Intestine", "Hodgkin's lymphoma of small intestine", "Hodgkin's Lymphoma of the Small Bowel", "Hodgkin's Disease of the Small Intestine", "Hodgkin's Lymphoma of the Small Intestine", "Primary Small Intestinal Hodgkin's Lymphoma", "Hodgkin's lymphoma of small intestine (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's lymphoma of small intestine", "shortest_name_length": 29}
{"curie": "UMLS:C4054654", "names": ["Leiomyosarcoma of Deep Soft Tissue", "Leiomyosarcoma of the Deep Soft Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leiomyosarcoma of Deep Soft Tissue", "shortest_name_length": 34}
{"curie": "MONDO:0019928", "names": ["XXXY Syndrome", "XXXY syndrome", "48,XXXY syndrome", "48, XXXY Syndrome", "48, XXXY syndrome", "XXXY syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "48,XXXY syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0020533", "names": ["Haverhill fever", "Haverhill Fever", "Haverhill; fever", "FEVER, HAVERHILL", "fever; Haverhill", "Streptobacillosis", "Streptobacillary fever", "streptobacillary; fever", "fever; streptobacillary", "Haverhill fever (diagnosis)", "Epidemic arthritic erythema", "erythema; epidemic, arthritic", "epidemic; erythema, arthritic", "Streptobacillary rat bite fever", "ERYTHEMA ARTHRITICUM EPIDEMICUM", "streptobacillary rat-bite fever", "Streptobacillary rat-bite fever", "Erythema arthriticum epidemicum", "Rat-bite streptobacillary fever", "RAT-BITE FEVER, STREPTOBACILLARY", "arthriticum epidemicum; erythema", "Streptobacillary fever (disorder)", "rat-bite fever Streptobacillus moniliformis", "rat-bite fever due to Streptobacillus moniliformis", "Rat-bite fever due to Streptobacillus moniliformis", "rat-bite; fever, due to Streptobacillus moniliformis", "fever; rat-bite, due to Streptobacillus moniliformis", "STREPTOBACILLUS MONILIFORMIS INFECTION RAT BITE FEVER", "STREPTOBACILLUS MONILIFORMIS INFECTION <RAT BITE FEVER>", "rat-bite fever due to Streptobacillus moniliformis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "streptobacillary rat-bite fever", "shortest_name_length": 15}
{"curie": "MONDO:0060711", "names": ["JABELS", "JABERI-ELAHI SYNDROME", "Jaberi-Elahi syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jaberi-Elahi syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0017670", "names": ["autosomal dominant diffuse mutilating palmoplantar keratoderma", "autosomal dominant diffuse mutilating palmoplantar hyperkeratosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant diffuse mutilating palmoplantar keratoderma", "shortest_name_length": 62}
{"curie": "UMLS:C0334031", "names": ["Epithelial nest", "Epithelial pearl", "Keratin pearl formation", "Keratin Pearls Formation", "Squamous Pearl Formation", "Squamous Pearls Formation", "Keratin pearl formation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Keratin pearl formation", "shortest_name_length": 15}
{"curie": "MONDO:0000816", "names": ["Metabolic Syndrome", "metabolic syndrome", "metabolic syndrome X", "Metabolic Syndrome X", "Cardiometabolic Syndrome", "abdominal obesity-metabolic syndrome", "abdominal obesity metabolic syndrome", "Abdominal obesity metabolic syndrome", "Abdominal Obesity-Metabolic Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "abdominal obesity-metabolic syndrome", "shortest_name_length": 18}
{"curie": "MONDO:0003388", "names": ["ampulla of Vater clear cell adenocarcinoma", "Ampulla of Vater Clear Cell Adenocarcinoma", "ampulla of vater clear cell adenocarcinoma", "hepatopancreatic ampulla clear cell adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ampulla of vater clear cell adenocarcinoma", "shortest_name_length": 42}
{"curie": "UMLS:C5205965", "names": ["Seminal Vesicle Leiomyoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Seminal Vesicle Leiomyoma", "shortest_name_length": 25}
{"curie": "UMLS:C0263377", "names": ["Sulzberger-Garbe syndrome", "Exudative discoid and lichenoid dermatosis", "Distinctive exudative discoid and lichenoid chronic dermatosis (Sulzberger and Garbe)", "Distinctive exudative discoid AND lichenoid chronic dermatosis of Sulzberger and Garbe", "Distinctive exudative discoid and lichenoid chronic dermatosis of Sulzberger and Garbe", "Distinctive exudative discoid AND lichenoid chronic dermatosis of Sulzberger and Garbe (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Distinctive exudative discoid AND lichenoid chronic dermatosis of Sulzberger and Garbe", "shortest_name_length": 25}
{"curie": "MONDO:0006388", "names": ["Malignant Prolactinoma", "malignant prolactinoma", "Malignant Pituitary Prolactinoma", "malignant pituitary prolactinoma", "Malignant Prolactinoma of Pituitary", "malignant prolactin producing tumor", "Malignant Prolactin Producing Tumor", "malignant prolactinoma of pituitary", "Metastatic Prolactin-Producing PitNET", "malignant pituitary gland prolactinoma", "Malignant Pituitary Gland Prolactinoma", "malignant prolactinoma of the pituitary", "PRL Producing Pituitary Gland Carcinoma", "Malignant Prolactinoma of the Pituitary", "PRL producing pituitary gland carcinoma", "Malignant Prolactinoma of Pituitary Gland", "malignant prolactinoma of pituitary gland", "Prolactin Producing Pituitary Gland Carcinoma", "malignant prolactinoma of the pituitary gland", "malignant prolactin secreting pituitary tumor", "Malignant Prolactin Secreting Pituitary Tumor", "Malignant Prolactinoma of the Pituitary Gland", "prolactin-producing pituitary gland carcinoma", "Prolactin-Producing Pituitary Gland Carcinoma", "Malignant Prolactin Producing Pituitary Tumor", "prolactin producing pituitary gland carcinoma", "malignant prolactin producing pituitary tumor", "Malignant Prolactin Secreting Tumor of Pituitary", "malignant prolactin producing tumor of pituitary", "malignant prolactin secreting pituitary neoplasm", "Malignant Prolactin Producing Pituitary Neoplasm", "Malignant Prolactin Secreting Pituitary Neoplasm", "malignant prolactin secreting tumor of pituitary", "Malignant Prolactin Producing Tumor of Pituitary", "malignant prolactin producing pituitary neoplasm", "Malignant Prolactin Secreting Neoplasm of Pituitary", "malignant prolactin producing neoplasm of pituitary", "Malignant Prolactin Secreting Pituitary Gland Tumor", "Malignant Prolactin Producing Pituitary Gland Tumor", "malignant prolactin secreting pituitary gland tumor", "Malignant Prolactin Producing Neoplasm of Pituitary", "malignant prolactin producing pituitary gland tumor", "malignant prolactin secreting neoplasm of pituitary", "Malignant Prolactin Producing Tumor of the Pituitary", "malignant prolactin producing tumor of the pituitary", "malignant prolactin secreting tumor of the pituitary", "Metastatic Lactotroph Pituitary Neuroendocrine Tumor", "Malignant Prolactin Secreting Tumor of the Pituitary", "Malignant Prolactin Secreting Pituitary Gland Neoplasm", "malignant prolactin producing pituitary gland neoplasm", "malignant prolactin producing tumor of pituitary gland", "Malignant Prolactin Secreting Tumor of Pituitary Gland", "malignant prolactin secreting pituitary gland neoplasm", "malignant prolactin secreting tumor of pituitary gland", "Malignant Prolactin Producing Pituitary Gland Neoplasm", "Malignant Prolactin Producing Tumor of Pituitary Gland", "malignant prolactin producing neoplasm of the pituitary", "malignant prolactin secreting neoplasm of the pituitary", "Malignant Prolactin Secreting Neoplasm of the Pituitary", "Malignant Prolactin Producing Neoplasm of the Pituitary", "malignant prolactin secreting neoplasm of pituitary gland", "malignant prolactin producing neoplasm of pituitary gland", "Malignant Prolactin Secreting Neoplasm of Pituitary Gland", "Malignant Prolactin Producing Neoplasm of Pituitary Gland", "malignant prolactin secreting tumor of the pituitary gland", "Malignant Prolactin Secreting Tumor of the Pituitary Gland", "malignant prolactin producing tumor of the pituitary gland", "Malignant Prolactin Producing Tumor of the Pituitary Gland", "malignant prolactin producing neoplasm of the pituitary gland", "malignant prolactin secreting neoplasm of the pituitary gland", "Malignant Prolactin Secreting Neoplasm of the Pituitary Gland", "Malignant Prolactin Producing Neoplasm of the Pituitary Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prolactin-producing pituitary gland carcinoma", "shortest_name_length": 22}
{"curie": "MONDO:0015488", "names": ["predominantly large-vessel vasculitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "predominantly large-vessel vasculitis", "shortest_name_length": 37}
{"curie": "UMLS:C4764275", "names": ["Non-Hodgkin Lymphoma in Remission", "Non-Hodgkin lymphoma in remission", "Non-Hodgkin's lymphoma in remission", "Non-Hodgkin lymphoma in remission (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Hodgkin's lymphoma in remission", "shortest_name_length": 33}
{"curie": "MONDO:0001525", "names": ["Calcitonin secretion disorder", "thyrocalcitonin secretion disease", "Disorder of thyrocalcitonin secretion", "disorder of thyrocalcitonin secretion", "Disorders of thyrocalcitonin secretion", "Disorder of thyrocalcitonin secretion (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyrocalcitonin secretion disease", "shortest_name_length": 29}
{"curie": "UMLS:C5206442", "names": ["Stage IB3 Cervical Cancer FIGO 2018", "Stage IB3 Cervical Carcinoma FIGO 2018"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB3 Cervical Cancer FIGO 2018", "shortest_name_length": 35}
{"curie": "UMLS:C0010673", "names": ["Endometrial cystic hyperplasia", "Cystic endometrial hyperplasia", "Cystic Endometrial Hyperplasia", "Cystic hyperplasia of endometrium", "Endometrial cystic hyperplasia (disorder)", "Swiss cheese hyperplasia of the endometrium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endometrial cystic hyperplasia", "shortest_name_length": 30}
{"curie": "MONDO:0012592", "names": ["OI11", "OI type 11", "OI type XI", "OI, type 11", "OI, TYPE XI", "FKBP10 osteogenesis imperfecta", "osteogenesis imperfecta type 11", "osteogenesis imperfecta type XI", "osteogenesis imperfecta, type 11", "osteogenesis imperfecta, type XI", "OSTEOGENESIS IMPERFECTA, TYPE XI", "osteogenesis imperfecta caused by mutation in FKBP10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteogenesis imperfecta type 11", "shortest_name_length": 4}
{"curie": "UMLS:C3829187", "names": ["Stage IIa", "Masaoka Stage IIa", "Masaoka-Koga Stage IIa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Masaoka-Koga Stage IIa", "shortest_name_length": 9}
{"curie": "UMLS:C4527186", "names": ["Stage IIIB", "Stage IIIB Cutaneous (Skin) Melanoma", "Pathologic Stage IIIB Cutaneous Melanoma AJCC v8", "Pathologic Stage IIIB Melanoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IIIB Cutaneous Melanoma AJCC v8", "shortest_name_length": 10}
{"curie": "MONDO:0060724", "names": ["GPIBD17", "glycosylphosphatidylinositol biosynthesis defect 17", "GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 17"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycosylphosphatidylinositol biosynthesis defect 17", "shortest_name_length": 7}
{"curie": "MONDO:0018781", "names": ["KIDAD", "KID syndrome", "syndrome kid", "kid syndrome", "kids syndrome", "Senter syndrome", "KID/HID syndrome", "Senter syndrome (disorder)", "ichthyosis hystrix Rheydt type", "Ichthyosis hystrix Rheydt type", "KID SYNDROME, AUTOSOMAL DOMINANT", "Kid Syndrome, Autosomal Dominant", "keratitis-ichthyosis-deafness syndrome", "Keratitis ichthyosis and deafness syndrome", "keratitis-ichthyosis-deafness (KID) syndrome", "KIDS - Keratitis ichthyosis and deafness syndrome", "keratitis, ichthyosis, and deafness (KID) syndrome", "Keratitis, Ichthyosis, and Deafness (KID) Syndrome", "KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT", "Keratitis-ichthyosis-deafness syndrome, autosomal dominant", "Autosomal dominant keratitis, ichthyosis, deafness syndrome", "Autosomal dominant KID (keratitis, ichthyosis, deafness) syndrome", "Keratitis-ichthyosis-deafness/Hystrix-like ichthyosis-deafness syndrome", "keratitis-ichthyosis-deafness/Hystrix-like ichthyosis-deafness syndrome", "Keratitis-ichthyosis-hearing loss/Hystrix-like ichthyosis-hearing loss syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "KID syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0032881", "names": ["POF16", "premature ovarian failure 16", "PREMATURE OVARIAN FAILURE 16", "primary ovarian insufficiency 16"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "premature ovarian failure 16", "shortest_name_length": 5}
{"curie": "UMLS:C5207072", "names": ["Refractory Colorectal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Colorectal Adenocarcinoma", "shortest_name_length": 36}
{"curie": "MONDO:0015531", "names": ["non-Langerhans cell histiocytosis", "non-Langerhans-cell histiocytosis", "Non-Langerhans-Cell Histiocytosis", "cell histiocytosis non langerhans", "Non-Langerhans cell histiocytosis", "Histiocytosis, Non Langerhans Cell", "Histiocytosis, Non-Langerhans-Cell", "histiocytosis, non-Langerhans-cell", "non-Langerhans cell histiocytosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-Langerhans cell histiocytosis", "shortest_name_length": 33}
{"curie": "MONDO:0001585", "names": ["Hallucinogen abuse", "hallucinogen abuse", "hallucinogens; abuse", "abuse; hallucinogens", "Hallucinogen abuse (disorder)", "hallucinogen abuse (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hallucinogen abuse", "shortest_name_length": 18}
{"curie": "MONDO:0020351", "names": ["Blake pouch cyst"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Blake pouch cyst", "shortest_name_length": 16}
{"curie": "UMLS:C5207073", "names": ["Paratesticular Melanotic Neuroectodermal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paratesticular Melanotic Neuroectodermal Tumor", "shortest_name_length": 46}
{"curie": "UMLS:C5204515", "names": ["Bladder Endometrioid Carcinoma", "Bladder Endometrioid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder Endometrioid Adenocarcinoma", "shortest_name_length": 30}
{"curie": "UMLS:C1706729", "names": ["Adult Heart Cellular Rhabdomyoma", "Adult Cardiac Cellular Rhabdomyoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Cardiac Cellular Rhabdomyoma", "shortest_name_length": 32}
{"curie": "UMLS:C0524610", "names": ["alcoholic hepatitis chronic", "Chronic alcoholic hepatitis", "Chronic Alcoholic Hepatitis", "Alcoholic Hepatitis, Chronic", "Hepatitis, Alcoholic, Chronic", "Chronic Alcoholic Hepatitides", "Chronic alcoholic hepatitis (disorder)", "Chronic alcoholic hepatitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic Alcoholic Hepatitis", "shortest_name_length": 27}
{"curie": "MONDO:0005189", "names": ["internal carotid artery stenosis", "artery carotid internal stenosis", "Internal carotid artery stenosis", "Internal Carotid Artery Stenosis", "carotid artery stenosis - internal", "ICA - Internal carotid artery stenosis", "Internal carotid artery stenosis (disorder)", "Internal carotid artery stenosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "internal carotid artery stenosis", "shortest_name_length": 32}
{"curie": "MONDO:0006294", "names": ["pleural tumor", "Pleural tumor", "pleura cancer", "Pleura--Cancer", "Pleural Cancer", "pleural cancer", "cancer of pleura", "Cancer of Pleura", "Cancer of pleura", "neoplasm of pleura", "Cancer of the Pleura", "cancer of the pleura", "CA - Cancer of pleura", "Malignant Pleural Tumor", "malignant pleural tumor", "Malignant tumor of pleura", "malignant pleura neoplasm", "Malignant Tumor of Pleura", "malignant tumor of pleura", "malignant pleural neoplasm", "Malignant Pleural Neoplasm", "Malignant tumour of pleura", "malignant neoplasm of pleura", "Malignant Neoplasm of Pleura", "Malignant neoplasm of pleura", "Malignant Tumor of the Pleura", "malignant tumor of the pleura", "Malignant neoplasm of pleura NOS", "malignant neoplasm of the pleura", "Malignant Neoplasm of the Pleura", "Malignant neoplasm of pleura, NOS", "Malignant tumor of pleura (disorder)", "malignant neoplasm of pleura (diagnosis)", "Malignant neoplasm of pleura, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pleural cancer", "shortest_name_length": 13}
{"curie": "MONDO:0013170", "names": ["URDS", "ARCL1C", "cutis laxa type IC", "Urban Rifkin Davis syndrome", "Urban-Rifkin-Davis syndrome", "Urban-Rifkin-Davis Syndrome", "URBAN-RIFKIN-DAVIS SYNDROME", "cutis laxa type IC (diagnosis)", "autosomal recessive cutis laxa type IC", "autosomal recessive cutis laxa type 1C", "Autosomal recessive cutis laxa type 1C", "CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IC", "cutis laxa, autosomal recessive, type 1C", "cutis laxa, autosomal recessive, type IC", "ARCL1C - autosomal recessive cutis laxa type 1C", "Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies", "cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies", "Cutis Laxa With Severe Pulmonary, Gastrointestinal, And Urinary Abnormalities", "cutis laxa with Severe pulmonary, gastrointestinal, and urinary abnormalities", "CUTIS LAXA WITH SEVERE PULMONARY, GASTROINTESTINAL, AND URINARY ABNORMALITIES", "Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies", "shortest_name_length": 4}
{"curie": "MONDO:0009191", "names": ["LWS", "LOWRY-WOOD SYNDROME", "Lowry Wood syndrome", "Lowry-Wood Syndrome", "Lowry-Wood syndrome", "Lowry-Wood syndrome (LWS)", "Epiphyseal dysplasia, microcephaly and nystagmus", "epiphyseal dysplasia, microcephaly and nystagmus", "epiphyseal dysplasia, microcephaly, and NYSTAGMUS", "Epiphyseal Dysplasia, Microcephaly, And Nystagmus", "Epiphyseal dysplasia-microcephaly-nystagmus syndrome", "epiphyseal dysplasia-microcephaly-nystagmus syndrome", "Epiphyseal dysplasia, microcephalus, nystagmus syndrome", "epiphyseal dysplasia-short stature-microcephaly-nystagmus syndrome", "Epiphyseal dysplasia, microcephalus, nystagmus syndrome (disorder)", "EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MICROCEPHALY AND RETINAL DYSTROPHY", "short stature-microcephaly-mental retardation-multiple epiphyseal dysplasia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lowry-Wood syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C1112276", "names": ["postoperative thoracic procedure complication", "Thoracic Procedure Postoperative Complication", "Postoperative thoracic procedure complication", "postoperative thoracic procedure complication (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thoracic Procedure Postoperative Complication", "shortest_name_length": 45}
{"curie": "MONDO:0021288", "names": ["hypopharynx cancer, stage 0", "Cancer in situ of hypopharynx", "hypopharynx in situ carcinoma", "Stage 0 Hypopharynx Carcinoma", "Stage 0 Hypopharyngeal Cancer", "stage 0 hypopharynx carcinoma", "stage 0 hypopharyngeal cancer", "hypopharynx carcinoma in situ", "Hypopharyngeal cancer stage 0", "Hypopharynx Carcinoma in situ", "hypopharyngeal cancer, stage 0", "hypopharyngeal carcinoma in situ", "stage 0 carcinoma of hypopharynx", "Stage 0 Hypopharyngeal Carcinoma", "carcinoma in situ of hypopharynx", "Stage 0 Carcinoma of Hypopharynx", "Hypopharyngeal Carcinoma in situ", "Carcinoma in situ of Hypopharynx", "stage 0 hypopharyngeal carcinoma", "Carcinoma in situ of hypopharynx", "Carcinoma in situ of laryngopharynx", "Carcinoma in situ of the Hypopharynx", "Stage 0 Carcinoma of the Hypopharynx", "stage 0 carcinoma of the hypopharynx", "stage 0 hypopharyngeal throat cancer", "Stage 0 Hypopharyngeal Throat Cancer", "Carcinoma In Situ of the Hypopharynx", "carcinoma in situ of the hypopharynx", "Carcinoma in situ of hypopharynx, NOS", "Stage 0 Hypopharyngeal Carcinoma AJCC v6", "Stage 0 Hypopharyngeal Carcinoma AJCC v7", "Stage 0 Hypopharyngeal Carcinoma AJCC v8", "stage 0 hypopharyngeal carcinoma aJCC v8", "stage 0 hypopharyngeal carcinoma aJCC v7", "stage 0 hypopharyngeal carcinoma in situ", "stage 0 hypopharyngeal carcinoma aJCC v6", "Carcinoma in situ of hypopharynx (disorder)", "carcinoma in situ of hypopharynx (diagnosis)", "stage 0 hypopharyngeal carcinoma aJCC v6, v7, and v8", "Stage 0 Hypopharyngeal Carcinoma AJCC v6, v7, and v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma in situ of hypopharynx", "shortest_name_length": 27}
{"curie": "MONDO:0010036", "names": ["CSD", "DIAR3", "SPINT2 secretory diarrhea", "SODIUM DIARRHEA, CONGENITAL", "sodium diarrhea, congenital", "Sodium Diarrhea, Congenital", "congenital secretory sodium diarrhea 3", "congenital secretory sodium diarrhoea 3", "Diarrhea 3, Secretory Sodium, Congenital", "congenital secretory sodium diarrhea type 3", "secretory diarrhea caused by mutation in SPINT2", "congenital secretory sodium diarrhea 3 syndromic", "congenital secretory sodium diarrhoea 3 syndromic", "Diarrhea 3, Secretory Sodium, Congenital, Syndromic", "DIARRHEA 3, SECRETORY SODIUM, CONGENITAL, SYNDROMIC", "diarrhea 3, secretory sodium, congenital, syndromic", "congenital secretory sodium diarrhea 3 with or without other congenital anomalies", "congenital secretory sodium diarrhoea 3 with or without other congenital anomalies", "diarrhea 3, secretory sodium, congenital, with or without other congenital anomalies", "DIARRHEA 3, SECRETORY SODIUM, CONGENITAL, WITH OR WITHOUT OTHER CONGENITAL ANOMALIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital secretory sodium diarrhea 3", "shortest_name_length": 3}
{"curie": "MONDO:0021176", "names": ["Type 2 AIH", "AIH type 2", "type 2 AIH", "Type 2 Autoimmune Hepatitis", "autoimmune hepatitis type 2", "Autoimmune hepatitis type 2", "Autoimmune Hepatitis, Type 2", "Autoimmune hepatitis type 2 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune hepatitis type 2", "shortest_name_length": 10}
{"curie": "MONDO:0015212", "names": ["syndromic intestinal malformation", "syndrome associated with intestinal malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic intestinal malformation", "shortest_name_length": 33}
{"curie": "MONDO:0008099", "names": ["CSNBAD2", "PDE6B congenital stationary night blindness", "Rambusch type congenital stationary night blindness", "Night Blindness, Congenital Stationary, Rambusch Type", "night blindness, congenital stationary, Rambusch type", "NIGHT BLINDNESS, CONGENITAL STATIONARY, RAMBUSCH TYPE", "congenital stationary night blindness autosomal dominant 2", "NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 2", "night blindness, congenital stationary, autosomal dominant 2", "Night Blindness, Congenital Stationary, Autosomal Dominant 2", "congenital stationary night blindness autosomal dominant type 2", "congenital stationary night blindness caused by mutation in PDE6B", "night blindness, congenital stationary, autosomal dominant type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital stationary night blindness autosomal dominant 2", "shortest_name_length": 7}
{"curie": "MONDO:0005179", "names": ["ovarian adenoma benign"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian adenoma benign", "shortest_name_length": 22}
{"curie": "UMLS:C5556446", "names": ["Refractory Superficial Bladder Urothelial Carcinoma", "Refractory Superficial Bladder Transitional Cell Carcinoma", "Refractory Non-Muscle Invasive Bladder Urothelial Carcinoma", "Refractory Non-Muscle Invasive Bladder Transitional Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Non-Muscle Invasive Bladder Urothelial Carcinoma", "shortest_name_length": 51}
{"curie": "UMLS:C4682797", "names": ["Testicular Cancer by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular Cancer by AJCC v8 Stage", "shortest_name_length": 34}
{"curie": "UMLS:C1541316", "names": ["Giant Cell Glioblastoma", "adult giant cell glioblastoma", "Adult Giant Cell Glioblastoma", "giant cell glioblastoma, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Giant Cell Glioblastoma", "shortest_name_length": 23}
{"curie": "UMLS:C4526609", "names": ["Stage III Thymoma", "Stage III Thymoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Thymoma AJCC v8", "shortest_name_length": 17}
{"curie": "MONDO:0018442", "names": ["Retinoid embryopathy", "retinoid embryopathy", "Acitretin embryopathy", "acitretin embryopathy", "Fetal acitretin syndrome", "fetal acitretin syndrome", "acitretin embryofetopathy", "Foetal acitretin syndrome", "Acitretin embryofetopathy", "Acitretin embryofoetopathy", "Acitretine embryofetopathy", "Embryopathy caused by retinoid", "Embryopathy caused by acitretin", "acitretin/etretinate embryopathy", "Acitretin/etretinate embryopathy", "Fetal acitretin/etretinate syndrome", "fetal acitretin/etretinate syndrome", "Embryopathy caused by retinoid (disorder)", "Embryopathy caused by acitretin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acitretin/etretinate embryopathy", "shortest_name_length": 20}
{"curie": "UMLS:C1512748", "names": ["Urothelial carcinoma with squamous differentiation", "Infiltrating Bladder Urothelial Carcinoma with Squamous", "Infiltrating Bladder Urothelial Carcinoma with Squamous Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infiltrating Bladder Urothelial Carcinoma with Squamous Differentiation", "shortest_name_length": 50}
{"curie": "MONDO:0003710", "names": ["mixed germ cell tumor", "ovary mixed germ cell tumor", "ovarian mixed germ cell tumor", "Ovarian germ cell tumor mixed", "Ovarian Mixed Germ Cell Tumor", "Ovarian germ cell tumour mixed", "mixed germ cell tumor, ovarian", "Mixed Germ Cell Tumor of Ovary", "mixed germ cell tumor of Ovary", "mixed germ cell tumor of ovary", "germ cell tumor, mixed, ovarian", "Ovarian Mixed Germ Cell Neoplasm", "ovarian mixed germ cell neoplasm", "mixed germ cell neoplasm of ovary", "Mixed Germ Cell Neoplasm of Ovary", "Mixed Germ Cell Tumor of the Ovary", "mixed germ cell tumor of the ovary", "mixed germ cell neoplasm of the ovary", "Mixed Germ Cell Neoplasm of the Ovary", "malignant mixed germ cell tumor of ovary", "malignant mixed germ cell tumor of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian mixed germ cell neoplasm", "shortest_name_length": 21}
{"curie": "MONDO:0010880", "names": ["HHT2", "ORW2", "OSLER-RENDU-WEBER SYNDROME 2", "Osler-rendu-weber syndrome 2", "Osler Weber Rendu syndrome type 2", "telangiectasia hereditary hemorrhagic type 2", "hereditary hemorrhagic telangiectasia type 2", "ACVRL1 hereditary hemorrhagic telangiectasia", "telangiectasia, hereditary hemorrhagic, type 2", "TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2", "Telangiectasia, hereditary hemorrhagic, type 2", "hereditary hemorrhagic telangiectasia caused by mutation in ACVRL1", "HEREDITARY HEMORRHAGIC TELANGIECTASIA-RELATED PULMONARY ARTERIAL HYPERTENSION", "Hereditary Hemorrhagic Telangiectasia-Related Pulmonary Arterial Hypertension", "pulmonary arterial hypertension, hereditary hemorrhagic telangiectasia-related", "Pulmonary Arterial Hypertension, Hereditary Hemorrhagic Telangiectasia-Related", "PULMONARY ARTERIAL HYPERTENSION, HEREDITARY HEMORRHAGIC TELANGIECTASIA-RELATED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "telangiectasia, hereditary hemorrhagic, type 2", "shortest_name_length": 4}
{"curie": "UMLS:C4302369", "names": ["Primary thymic carcinoma", "Primary thymic carcinoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary thymic carcinoma", "shortest_name_length": 24}
{"curie": "UMLS:C2973787", "names": ["Coxiella burnetii Infection", "Coxiella burnetii Infections", "Infection, Coxiella burnetii", "Infections, Coxiella burnetii", "Coxiella burnetii Vector Borne Disease", "Coxiella burnetii Vector-Borne Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Coxiella burnetii Infection", "shortest_name_length": 27}
{"curie": "UMLS:C1265601", "names": ["Single mass", "Solitary mass", "Solitary Mass", "solitary mass", "Solitary mass (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Solitary mass", "shortest_name_length": 11}
{"curie": "UMLS:C4525304", "names": ["stage IIIB gallbladder cancer", "Stage IIIB Gallbladder Cancer", "Stage IIIB Gallbladder Cancer AJCC v8", "Stage IIIB Gallbladder Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Gallbladder Cancer AJCC v8", "shortest_name_length": 29}
{"curie": "MONDO:0007930", "names": ["BSSA2", "Bernard-Soulier syndrome type A2", "Bernard-Soulier syndrome, type A2 (dominant)", "Bernard-Soulier syndrome, type A2, autosomal dominant", "BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bernard-Soulier syndrome, type A2, autosomal dominant", "shortest_name_length": 5}
{"curie": "UMLS:C0574786", "names": ["Acute renal failure with medullary necrosis", "Acute kidney failure with medullary necrosis", "Acute renal papillary necrosis with renal failure", "Acute Renal Failure with Renal Papillary Necrosis", "Acute renal failure with lesion of renal medullary necrosis", "Acute renal papillary necrosis with renal failure (disorder)", "insufficiency; renal, acute, with necrosis, medullary, medullary", "kidney; insufficiency, acute, with necrosis, medullary, medullary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute renal papillary necrosis with renal failure", "shortest_name_length": 43}
{"curie": "MONDO:0000992", "names": ["Other heart block", "heart rhythm disease", "heart conduction disease", "cardiac conduction disease", "conduction disease of heart", "cardiac conduction disorder", "disease of cardiac conduction", "disorder of cardiac conduction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heart conduction disease", "shortest_name_length": 17}
{"curie": "MONDO:0010347", "names": ["MRX84", "XLID84", "X-linked mental retardation 84", "mental retardation, X-linked 84", "Mental Retardation, X-Linked 84", "MENTAL RETARDATION, X-LINKED 84", "intellectual disability, X-linked 84", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 84", "non-syndromic X-linked intellectual disability 84", "mental retardation, X-linked 84, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 84", "shortest_name_length": 5}
{"curie": "MONDO:0020509", "names": ["secondary syringomyelia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary syringomyelia", "shortest_name_length": 23}
{"curie": "MONDO:0005562", "names": ["ARHI", "age-related hearing impairment"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "age-related hearing impairment", "shortest_name_length": 4}
{"curie": "MONDO:0011294", "names": ["SCZD5", "SCHIZOPHRENIA 5", "schizophrenia 5", "schizophrenia 5 with or without an affective disorder", "SCHIZOPHRENIA 5 WITH OR WITHOUT AN AFFECTIVE DISORDER", "SCHIZOPHRENIA SUSCEPTIBILITY LOCUS, CHROMOSOME 6q-RELATED", "schizophrenia susceptibility locus, chromosome 6Q-related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schizophrenia 5", "shortest_name_length": 5}
{"curie": "MONDO:0011592", "names": ["EVR3", "EXUDATIVE VITREORETINOPATHY 3", "exudative vitreoretinopathy 3", "Exudative Vitreoretinopathy 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exudative vitreoretinopathy 3", "shortest_name_length": 4}
{"curie": "UMLS:C0279634", "names": ["pediatric acute M1 leukemia", "Pediatric Acute M1 Leukemia", "Childhood Acute M1 Leukemia", "childhood acute M1 leukemia", "M1 leukemia, childhood acute", "childhood AML without maturation", "Childhood AML without Maturation", "Pediatric AML without Maturation", "M1 childhood AML without maturation", "M1 Pediatric Acute Myelogenous Leukemia", "Acute Myeloid Leukemia (AML) without Maturation", "Pediatric Acute Myeloid Leukemia without Maturation", "Childhood Acute Myeloid Leukemia without Maturation", "M1 Childhood Acute Myeloid Leukemia without Maturation", "M1 Pediatric Acute Myeloid Leukemia without Maturation", "Childhood Acute Myelocytic Leukemia without Maturation", "Pediatric Acute Myelocytic Leukemia without Maturation", "Pediatric Acute Myelogenous Leukemia without Maturation", "Childhood Acute Myelogenous Leukemia without Maturation", "Childhood Acute Myeloblastic Leukemia without Maturation", "pediatric acute myeloblastic leukemia without maturation", "Pediatric Acute Myeloblastic Leukemia without Maturation", "M1 Childhood Acute Myelocytic Leukemia without Maturation", "M1 Pediatric Acute Myelocytic Leukemia without Maturation", "M1 Childhood Acute Myelogenous Leukemia without Maturation", "M1 Pediatric Acute Myelogenous Leukemia without Maturation", "M1 childhood acute myeloblastic leukemia without maturation", "M1 Pediatric Acute Myeloblastic Leukemia without Maturation", "M1 pediatric acute myeloblastic leukemia without maturation", "M1 Childhood Acute Myeloblastic Leukemia without Maturation", "Childhood Acute Myeloblastic Leukemia Without Maturation (M1)", "childhood acute myeloblastic leukemia without maturation (M1)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Acute Myeloid Leukemia without Maturation", "shortest_name_length": 27}
{"curie": "UMLS:C5237190", "names": ["Unresectable Clear Cell Renal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Clear Cell Renal Cell Carcinoma", "shortest_name_length": 44}
{"curie": "MONDO:0005280", "names": ["PROSTATITIS", "prostatitis", "Prostatitis", "Prostatitides", "Prostatitis NOS", "Prostatitis, NOS", "Urethroprostatitis", "prostate inflammation", "prostatitis (disease)", "prostate; inflammation", "inflammation; prostate", "Prostatitis (disorder)", "prostatitis (diagnosis)", "Prostatitis, unspecified", "Inflammation of prostate", "prostate gland inflammation", "Inflammation of the prostate", "Prostatic inflammatory disease", "inflammation of prostate gland", "Inflammatory diseases of prostate", "Inflammatory disease of prostate, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostatitis", "shortest_name_length": 11}
{"curie": "UMLS:C1697642", "names": ["Puncture site pain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Puncture site pain", "shortest_name_length": 18}
{"curie": "MONDO:0011528", "names": ["HIGM2", "AID deficiency", "aid deficiency", "HIGM2 Syndrome", "HIGM2 Syndromes", "hyper-IgM syndrome 2", "hyper IgM syndrome 2", "Hyper IgM Syndrome 2", "Hyper-IgM Syndrome 2", "HYPER-IgM SYNDROME 2", "AICDA hyper-IgM syndrome", "hyper-IgM syndrome type 2", "Hyper-IgM syndrome type 2", "immunodeficiency with hyper IgM type 2", "immunodeficiency with hyper-IgM type 2", "Immunodeficiency with Hyper-IgM Type 2", "Autosomal recessive hyper-IgM syndrome", "Immunodeficiency with Hyper IgM, Type 2", "IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 2", "Immunodeficiency with Hyper-IgM, Type 2", "immunodeficiency with hyper-IgM, type 2", "Hyper-IgM Immunodeficiency Syndrome Type 2", "Hyper IgM Immunodeficiency Syndrome Type 2", "Hyper-IgM Immunodeficiency Syndrome, Type 2", "Hyper IgM Immunodeficiency Syndrome, Type 2", "hyper-IgM syndrome caused by mutation in AICDA", "Activation-induced cytidine deaminase deficiency", "activation-induced cytidine deaminase deficiency", "Autosomal recessive hyperimmunoglobulin M syndrome", "Autosomal recessive hyper- immunoglobulin M syndrome", "autosomal recessive immunodeficiency with increased IgM", "immunodeficiency with increased IgM: autosomal recessive", "Autosomal recessive hyperimmunoglobulin M syndrome (disorder)", "autosomal recessive immunodeficiency with increased IgM (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyper-IgM syndrome type 2", "shortest_name_length": 5}
{"curie": "MONDO:0002239", "names": ["postsurgical hypoinsulinemia", "Postsurgical hypoinsulinemia", "post-surgical hypoinsulinemia", "Post-surgical hypoinsulinemia", "Postsurgical hypoinsulinaemia", "Hypoinsulinemia postoperative", "Postoperative hypoinsulinemia", "Post surgical hypoinsulinemia", "Postoperative hypoinsulinaemia", "Post-surgical hypoinsulinaemia", "Post surgical hypoinsulinaemia", "Hypoinsulinaemia postoperative", "Post-surgical hypoinsulinemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "post-surgical hypoinsulinemia", "shortest_name_length": 28}
{"curie": "MONDO:0008525", "names": ["Syringomyelia, Isolated", "syringomyelia, isolated", "syringomyelia, noncommunicating isolated", "SYRINGOMYELIA, NONCOMMUNICATING ISOLATED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syringomyelia, isolated", "shortest_name_length": 23}
{"curie": "UMLS:C4527003", "names": ["Retroperitoneal Sarcoma by AJCC v8 Stage", "Soft Tissue Sarcoma Retroperitoneum by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retroperitoneal Sarcoma by AJCC v8 Stage", "shortest_name_length": 40}
{"curie": "UMLS:C5690757", "names": ["CINAC", "KDUCAL", "Uncertain Etiology CKD", "Mesoamerican Nephropathy", "Nephropathy, Mesoamerican", "CKD of Uncertain Etiology", "Mesoamerican Nephropathies", "Chronic Kidney Disease of Unknown Etiology", "Chronic Kidney Disease of Uncertain Etiology", "Chronic Kidney Diseases of Uncertain Etiology", "CKDu Chronic Kidney Disease of Unknown Etiology", "Chronic Kidney Disease of Nontraditional Etiology", "CKDu Chronic Kidney Disease of Uncertain Etiology", "CKDu Chronic Kidney Diseases of Uncertain Etiology", "Chronic Kidney Disease of Unknown or Uncertain Etiology", "Kidney Disease of Unknown Cause in Agricultural Laborers", "Chronic Interstitial Nephritis of Agricultural Communities", "CINAC Chronic Interstitial Nephritis in Agricultural Communities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic Kidney Diseases of Uncertain Etiology", "shortest_name_length": 5}
{"curie": "UMLS:C4725820", "names": ["Recurrent Malignant Skin Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Malignant Skin Neoplasm", "shortest_name_length": 33}
{"curie": "MONDO:0019944", "names": ["Eisenmenger", "Eisenmenger Complex", "Eisenmenger complex", "defect; Eisenmenger", "eisenmenger complex", "Eisenmenger; defect", "EISENMENGER COMPLEX", "Eisenmenger Syndrome", "Eisenmenger; complex", "complex; Eisenmenger", "Eisenmenger's defect", "EISENMENGER SYNDROME", "Eisenmengers Complex", "eisenmengers complex", "Eisenmenger syndrome", "eisenmenger syndrome", "Complex, Eisenmenger", "Eisenmenger's Complex", "Eisenmenger's complex", "Syndrome, Eisenmenger", "eisenmengers syndrome", "eisenmenger's complex", "Eisenmengers Syndrome", "Complex, Eisenmenger's", "Eisenmenger's Syndrome", "eisenmenger's syndrome", "Eisenmenger's syndrome", "Syndrome, Eisenmenger's", "Eisenmenger's physiology", "Eisenmenger's defect or complex", "Eisenmenger's complex (disorder)", "Eisenmenger's syndrome (disorder)", "Eisenmenger's syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eisenmenger syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0032761", "names": ["DFNB114", "autosomal recessive deafness 114", "DEAFNESS, AUTOSOMAL RECESSIVE 114", "deafness, autosomal recessive 114", "hearing loss, autosomal recessive 114", "autosomal recessive nonsyndromic deafness 114"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal recessive 114", "shortest_name_length": 7}
{"curie": "MONDO:0007503", "names": ["EAR WITHOUT HELIX", "ear without helix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ear without helix", "shortest_name_length": 17}
{"curie": "MONDO:0001993", "names": ["Seminal Vesicle Adenocarcinoma", "seminal vesicle adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "seminal vesicle adenocarcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0042726", "names": ["Kuzniecky Andermann syndrome", "Macrogyria, pseudobulbar palsy and mental retardation", "macrogyria, pseudobulbar palsy and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macrogyria, pseudobulbar palsy and intellectual disability", "shortest_name_length": 28}
{"curie": "MONDO:0018805", "names": ["biliary cyst", "choledochocele", "Choledochocele", "CHOLEDOCHOCELE", "Choledochocyst", "choledochocyst", "Bile Duct Cyst", "bile duct cyst", "BILE DUCT CYSTS", "Cyst, Bile Duct", "Choledochocoele", "Duct Cyst, Bile", "choledochocoele", "Choledochoceles", "bile duct cysts", "Bile Duct Cysts", "Choledochal Cyst", "choledochal cyst", "Choledochal cyst", "choledochus cyst", "cyst choledochal", "CHOLEDOCHAL CYSTS", "CHOLEDOCHUS, CYST", "cyst; choledochus", "choledochal cysts", "Choledochal Cysts", "choledochus; cyst", "Cyst, Choledochal", "Choledochocele (disorder)", "Type III choledochal cyst", "Choledochal Cyst, Type III", "Choledochal cyst (disorder)", "Congenital common duct cyst", "Congenital Choledochal Cyst", "congenital choledochal cyst", "Congenital choledochal cyst", "Congenital Choledochal Cysts", "choledochal cyst (diagnosis)", "Choledochal Cyst, Congenital", "Congenital biliary duct cyst", "Cyst, Congenital Choledochal", "Cyst of the ductus choledochus", "BILE DUCT, COMMON, CYSTIC DILATATION", "Cystic dilatation of common bile duct", "Congenital choledochal cyst (disorder)", "congenital choledochal cyst (diagnosis)", "Cystic dilatation of wall of biliary tract", "Congenital choledochal cyst of common bile duct", "Congenital cystic dilatation of common bile duct", "Cystic dilatation of common bile duct (disorder)", "Congenital cystic dilatation of the biliary tract", "congenital cystic dilatation of the biliary tract", "Congenital cystic dilatation of wall of biliary tract", "Congenital cystic dilatation of common bile duct (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bile duct cyst", "shortest_name_length": 12}
{"curie": "UMLS:C0279704", "names": ["Malignant Type B1 Thymoma", "Thymoma, type B1, malignant", "Thymoma, organoid, malignant", "Lymphocytic malignant thymoma", "Thymoma, lymphocytic, malignant", "Thymoma, lymphocyte-rich, malignant", "Thymoma, predominantly cortical, malignant", "Thymoma, type B1, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thymoma, type B1, malignant", "shortest_name_length": 25}
{"curie": "MONDO:0020527", "names": ["ectopic Cushing syndrome", "ectopic ACTH secreting tumor", "occult ectopic ACTH secretion", "paraneoplastic Cushing syndrome", "adrenocorticotropic hormone secretion syndrome", "Cushing syndrome due to ectopic ACTH secretion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectopic Cushing syndrome", "shortest_name_length": 24}
{"curie": "MONDO:0003863", "names": ["MMNST", "Melanotic MPNST", "Melanocytic MPNST", "melanocytic MPNST", "malignant melanotic schwannoma", "Malignant melanotic Schwannoma", "Malignant melanotic schwannoma", "Malignant melanotic neurilemmoma", "Malignant Melanotic Schwannian Tumor", "Malignant Melanotic Nerve Sheath Tumor", "Melanotic malignant nerve sheath tumor", "malignant melanotic nerve sheath tumor", "melanotic malignant nerve sheath tumor", "Melanotic malignant nerve sheath tumour", "Malignant Melanotic Peripheral Nerve Sheath Tumor", "Melanotic malignant nerve sheath tumor (disorder)", "Melanotic malignant peripheral nerve sheath tumor", "malignant melanotic peripheral nerve sheath tumor", "melanotic malignant peripheral nerve sheath tumor", "malignant melanotic nerve sheath tumor (diagnosis)", "Melanotic malignant peripheral nerve sheath tumour", "melanotic malignant peripheral nerve sheath tumour", "Malignant Melanocytic Peripheral Nerve Sheath Tumor", "malignant melanocytic peripheral nerve sheath tumor", "Malignant Melanocytic Neoplasm of Peripheral Nerve Sheath", "malignant melanocytic neoplasm of peripheral nerve sheath", "malignant melanocytic neoplasm of the peripheral nerve sheath", "Malignant Melanocytic Neoplasm of the Peripheral Nerve Sheath", "Melanotic malignant peripheral nerve sheath tumor (morphologic abnormality)", "melanotic malignant peripheral nerve sheath tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant melanocytic neoplasm of the peripheral nerve sheath", "shortest_name_length": 5}
{"curie": "UMLS:C0235883", "names": ["Uterine inflammation", "UTERINE INFLAMMATION", "uterine inflammation", "Uterine inflammation NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine inflammation", "shortest_name_length": 20}
{"curie": "MONDO:0012055", "names": ["LRSL", "Lrsl", "Larsen-Like Syndrome", "LARSEN-LIKE SYNDROME", "Larsen-like syndrome", "Larsen-like syndrome, isolated cases", "Larsen-like osseous dysplasia-short stature syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Larsen-like osseous dysplasia-short stature syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C1709154", "names": ["Nasopharyngeal Paraganglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasopharyngeal Paraganglioma", "shortest_name_length": 28}
{"curie": "MONDO:0011380", "names": ["CLE", "VWM", "CACH", "CACH/VWM", "CACH Syndrome", "CACH syndrome", "CACH Syndromes", "CACH/VWM syndrome", "CACH VWM Syndrome", "CACH VWM Syndromes", "VWM Syndrome, CACH", "Syndrome, CACH VWM", "ovarioleukodystrophy", "Cree leukoencehalopathy", "Cree Leukoencephalopathy", "CREE LEUKOENCEPHALOPATHY", "Cree leukoencephalopathy", "Leukoencephalopathy, Cree", "Cree Leukoencephalopathies", "Myelinosis Centralis Diffusa", "myelinosis centralis diffusa", "Myelinosis centralis diffusa", "Diffusa, Myelinosis Centralis", "Centralis Diffusa, Myelinosis", "Myelinosis Centralis Diffusas", "Vanishing White Matter Disease", "Diffusas, Myelinosis Centralis", "vanishing white matter disease", "Vanishing white matter disease", "VANISHING WHITE MATTER LEUKODYSTROPHY", "vanishing white matter leukodystrophy", "Vanishing White Matter Leukodystrophy", "vanishing White matter leukodystrophy", "Vanishing white matter disease (disorder)", "Leukoencephalopathy with vanishing white matter", "LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER", "leukoencephalopathy with vanishing WHITE matter", "Leucoencephalopathy with vanishing white matter", "Leukoencephalopathy with Vanishing White Matter", "leukoencephalopathy with vanishing white matter", "leukoencephalopathy with vanishing white matter 1", "vanishing White matter leukodystrophy with ovarian failure", "childhood ataxia with central nervous system hypomyelination", "Childhood Ataxia with Central Nervous System Hypomyelination", "Childhood Ataxia with Central Nervous System Hypomyelinization", "childhood ataxia with central nervous system hypomyelinization", "CHILDHOOD ATAXIA WITH CENTRAL NERVOUS SYSTEM HYPOMYELINIZATION", "Childhood ataxia with diffuse central nervous system hypomyelination", "childhood ataxia with diffuse central nervous system hypomyelination", "Childhood Ataxia with Diffuse Central Nervous System Hypomyelination", "childhood ataxia with central nervous system hypomyelination/vanishing white matter", "CACH (childhood ataxia with diffuse central nervous system hypomyelination) syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukoencephalopathy with vanishing white matter", "shortest_name_length": 3}
{"curie": "MONDO:0014612", "names": ["PFBMFT4", "PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 4", "pulmonary fibrosis and/or bone marrow failure, Telomere-related, 4", "pulmonary fibrosis and/or bone marrow failure, TELOMERE-RELATED, 4", "PARN pulmonary fibrosis and/or bone marrow failure, Telomere-related", "pulmonary fibrosis and/or bone marrow failure, Telomere-related, type 4", "pulmonary fibrosis and/or bone marrow failure, Telomere-related caused by mutation in PARN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary fibrosis and/or bone marrow failure, Telomere-related, 4", "shortest_name_length": 7}
{"curie": "UMLS:C1335154", "names": ["Ovarian Cellular Fibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Cellular Fibroma", "shortest_name_length": 24}
{"curie": "UMLS:C0685639", "names": ["THORACOSCHISIS", "Thoracoschisis", "Thoracoschisis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thoracoschisis", "shortest_name_length": 14}
{"curie": "UMLS:C1266136", "names": ["GIST, Benign", "GIST, benign", "Benign Gastrointestinal Stromal Tumor", "GASTROINTESTINAL STROMAL TUMOR, BENIGN", "Gastrointestinal stromal tumor, benign", "Gastrointestinal stromal tumour, benign", "Gastrointestinal stromal tumor, benign (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal stromal tumor, benign", "shortest_name_length": 12}
{"curie": "UMLS:C5420298", "names": ["Testicular Biphasic Mesothelioma", "Paratesticular Biphasic Mesothelioma", "Tunica Vaginalis Biphasic Mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paratesticular Biphasic Mesothelioma", "shortest_name_length": 32}
{"curie": "UMLS:C4527422", "names": ["Relapsed Abdominal Neuroendocrine Tumor", "Recurrent Abdominal Neuroendocrine Tumor", "Recurrent Abdominal Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Abdominal Neuroendocrine Neoplasm", "shortest_name_length": 39}
{"curie": "MONDO:0011833", "names": ["SCA21", "Spinocerebellar ataxia 21", "spinocerebellar ataxia 21", "SPINOCEREBELLAR ATAXIA 21", "Spinocerebellar ataxia type 21", "spinocerebellar ataxia type 21", "SCA21 Spinocerebellar ataxia 21", "Spinocerebellar ataxia type 21 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia type 21", "shortest_name_length": 5}
{"curie": "MONDO:0004259", "names": ["endocervical cancer", "Endocervical Cancer", "endocervix carcinoma", "Endocervical Carcinoma", "endocervical carcinoma", "Carcinoma of Endocervix", "carcinoma of endocervix", "Carcinoma of endocervix", "carcinoma of the endocervix", "endocervical adenocarcinoma", "Carcinoma of the Endocervix", "Endocervical Adenocarcinoma", "carcinoma of the Endocervix", "Carcinoma of endocervix (disorder)", "Carcinoma of endocervix (diagnosis)", "cervical neoplasm malignant endocervix carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endocervical carcinoma", "shortest_name_length": 19}
{"curie": "UMLS:C1333826", "names": ["Glomus Tumor of Uncertain Malignant Potential"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Glomus Tumor of Uncertain Malignant Potential", "shortest_name_length": 45}
{"curie": "MONDO:0032668", "names": ["DBA18", "Diamond-Blackfan anemia 18", "DIAMOND-BLACKFAN ANEMIA 18", "RPL18-related Diamond-Blackfan anemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diamond-Blackfan anemia 18", "shortest_name_length": 5}
{"curie": "UMLS:C3658302", "names": ["SJS-TEN", "Toxic epidermolysis", "Toxic Epidermal Necrolysis Stevens Johnson Syndrome", "Toxic Epidermal Necrolysis Stevens-Johnson Syndrome", "Stevens-Johnson Syndrome Toxic Epidermal Necrolysis", "Stevens Johnson Syndrome Toxic Epidermal Necrolysis", "Toxic Epidermal Necrolysis Stevens-Johnson Syndrome Spectrum", "Toxic Epidermal Necrolysis Stevens Johnson Syndrome Spectrum", "Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum", "Stevens Johnson Syndrome Toxic Epidermal Necrolysis Spectrum", "Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum", "Stevens-Johnson syndrome, toxic epidermal necrolysis spectrum", "Stevens-Johnson syndrome, toxic epidermal necrolysis spectrum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum", "shortest_name_length": 7}
{"curie": "MONDO:0700160", "names": ["Canine Mammary Adenoma", "canine mammary adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canine mammary adenoma", "shortest_name_length": 22}
{"curie": "UMLS:C0269841", "names": ["Tetanic Contraction", "tetanic contraction", "tetanic contractions", "Tetanic contractions", "Tetanic uterine contraction", "Tetanic uterine contractions", "Uterine contraction, tetanic", "Tetanic contractions of uterus", "tetanic contractions (diagnosis)", "Tetanic contractions of uterus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tetanic contractions of uterus", "shortest_name_length": 19}
{"curie": "MONDO:0021759", "names": ["fructose malabsorption", "dietary fructose intolerance", "acquired fructose intolerance", "intestinal fructose intolerance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired fructose intolerance", "shortest_name_length": 22}
{"curie": "UMLS:C1699694", "names": ["Cecal infection", "Cecal Infection", "Caecal infection", "intestinal infections cecum", "Cecal infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cecal Infection", "shortest_name_length": 15}
{"curie": "MONDO:0054701", "names": ["KLEFS2", "KLEEFSTRA SYNDROME 2", "Kleefstra syndrome 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kleefstra syndrome 2", "shortest_name_length": 6}
{"curie": "MONDO:0006769", "names": ["STOMACH ATONY", "gastropareses", "ATONY STOMACH", "Atony stomach", "Gastric atony", "GASTRIC ATONY", "gastroparesis", "gastric atony", "Gastropareses", "GASTROPARESIS", "Gastroparesis", "Stomach atony", "gastric atonia", "atony; stomach", "Gastric atonia", "Stasis;gastric", "Gastric Stasis", "Gastric stasis", "gastric stasis", "Gastric Stases", "Stasis, Gastric", "Gastroparalysis", "gastroparalysis", "Stases, Gastric", "Atony of stomach", "Paralysis gastric", "PARALYSIS GASTRIC", "gastric paralysis", "paralysis; stomach", "stomach; paralysis", "gastroparesis syndrome", "Gastroparesis syndrome", "gastroparesis (disease)", "Delayed gastric emptying", "delayed gastric emptying", "Gastroparesis (disorder)", "Gastric atonia (disorder)", "gastroparesis (diagnosis)", "Gastroparesis syndrome, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastroparesis", "shortest_name_length": 13}
{"curie": "MONDO:0044314", "names": ["RP78", "RETINITIS PIGMENTOSA 78", "retinitis pigmentosa 78"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 78", "shortest_name_length": 4}
{"curie": "MONDO:0800156", "names": ["inborn disorder of ornithine, proline and hydroxyproline metabolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of ornithine, proline and hydroxyproline metabolism", "shortest_name_length": 67}
{"curie": "MONDO:0021048", "names": ["Mastocytoma", "Benign Mastocytoma", "benign mastocytoma", "mastocytoma, benign", "Mastocytoma, Benign", "MAST cell tumor, benign", "MAST CELL TUMOR, BENIGN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign mastocytoma", "shortest_name_length": 11}
{"curie": "MONDO:0005223", "names": ["M0", "AMLMD", "FAB M0", "AML M0", "AML-M0", "M0 myeloid leukemia", "M0 Myeloid Leukemia", "Acute myeloblastic leukemia", "M0 acute myelocytic leukemia", "Acute myeloblastic leukaemia", "M0 acute myelogenous leukemia", "M0 Acute Myelogenous Leukemia", "Acute myeloblastic leukemia M0", "M0 acute granulocytic leukemia", "M0 acute myeloblastic leukemia", "M0 Acute Myeloblastic Leukemia", "AML with minimal differentiation", "AML with Minimal Differentiation", "Acute myeloid leukemia, minimal differentiation", "Acute myeloid leukaemia, minimal differentiation", "M0 Myeloid Leukemia with Minimal Differentiation", "Acute Myeloid Leukemia, Minimally Differentiated", "acute myeloid leukemia, minimally differentiated", "M0 myeloid leukemia with minimal differentiation", "Acute myelocytic leukemia, minimal differentiation", "Acute myelocytic leukaemia, minimal differentiation", "Acute Myeloid Leukemia with Minimal Differentiation", "Acute myeloid leukemia with minimal differentiation", "acute myeloid leukemia with minimal differentiation", "Acute myelogenous leukemia, minimal differentiation", "Acute myeloid leukaemia with minimal differentiation", "Minimally differentiated acute myeloblastic leukemia", "Acute myelogenous leukaemia, minimal differentiation", "minimally differentiated acute myeloblastic leukemia", "Acute granulocytic leukemia, minimal differentiation", "Acute myeloblastic leukemia, minimal differentiation", "Acute Myeloblastic Leukemia, Minimally Differentiated", "Acute granulocytic leukaemia, minimal differentiation", "acute myeloblastic leukemia, minimally differentiated", "Acute myeloblastic leukaemia, minimal differentiation", "acute myelocytic leukemia with minimal differentiation", "acute myelogenous leukemia with minimal differentiation", "Acute Myelogenous Leukemia with Minimal Differentiation", "Acute Myeloid Leukemia with Minimal Differentiation (MO)", "acute myeloblastic leukemia with minimal differentiation", "acute myeloid leukemia with minimal differentiation (MO)", "Acute Myeloblastic Leukemia with Minimal Differentiation", "M0 Acute Myelogenous Leukemia with Minimal Differentiation", "M0 acute myelogenous leukemia with minimal differentiation", "M0 acute granulocytic leukemia with minimal differentiation", "Acute myeloid leukemia, minimal differentiation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia with minimal differentiation", "shortest_name_length": 2}
{"curie": "MONDO:0007273", "names": ["PGL4", "Paragangliomas 4", "PARAGANGLIOMAS 4", "paragangliomas 4", "SDHB paraganglioma", "paragangliomas type 4", "PARAGANGLIOMA, FAMILIAL MALIGNANT", "paraganglioma, familial malignant", "Paraganglioma, Familial Malignant", "PHEOCHROMOCYTOMA, FAMILIAL EXTRAADRENAL", "Paragangliomas, Hereditary Extraadrenal", "PARAGANGLIOMAS, HEREDITARY EXTRAADRENAL", "pheochromocytoma, familial extraadrenal", "paragangliomas, hereditary extraadrenal", "Pheochromocytoma, Familial Extraadrenal", "paraganglioma caused by mutation in SDHB", "pheochromocytoma, extraadrenal and cervical paraganglioma", "PHEOCHROMOCYTOMA, EXTRAADRENAL, AND CERVICAL PARAGANGLIOMA", "pheochromocytoma, extraadrenal, and cervical paraganglioma", "Pheochromocytoma, Extraadrenal, and Cervical Paraganglioma", "Carotid Body Tumors and Multiple Extraadrenal Pheochromocytomas", "SDHB-related hereditary paraganglioma-pheochromocytoma syndrome", "CAROTID BODY TUMORS AND MULTIPLE EXTRAADRENAL PHEOCHROMOCYTOMAS", "carotid body tumors and multiple extraadrenal Pheochromocytomas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paragangliomas 4", "shortest_name_length": 4}
{"curie": "MONDO:0002241", "names": ["FXIIID", "Factor 13 Deficiency", "Deficiency, Factor 13", "Factor XIII Deficiency", "factor XIII deficiency", "Factor XIII deficiency", "Factor 13 Deficiencies", "Deficiency, factor XIII", "Deficiencies, Factor 13", "Deficiency, Factor XIII", "Factor XIII Deficiencies", "Deficiency of factor XIII", "Deficiencies, Factor XIII", "Factor Thirteen Deficiency", "Deficiency, Factor Thirteen", "Factor Thirteen Deficiencies", "Deficiencies, Factor Thirteen", "Deficiency, Laki-Lorand factor", "FIBRINASE DEFICIENCY, CONGENITAL", "Hereditary Factor XIII Deficiency", "Congenital factor XIII deficiency", "congenital factor XIII deficiency", "FACTOR XIII DEFICIENCY, CONGENITAL", "Factor XIII deficiency disease, NOS", "Fibrin-stabilizing factor deficiency", "Fibrin stabilizing factor deficiency", "fibrin; stabilizing factor deficiency", "Laki-Lorand factor deficiency disease", "deficiency; fibrin-stabilizing factor", "LAKI-LORAND FACTOR DEFICIENCY, CONGENITAL", "Hereditary factor XIII deficiency disease", "congenital factor XIII deficiency (diagnosis)", "Hereditary Fibrin Stabilizing Factor Deficiency", "FIBRIN STABILIZING FACTOR DEFICIENCY, CONGENITAL", "Hereditary factor XIII deficiency disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "factor XIII deficiency", "shortest_name_length": 6}
{"curie": "UMLS:C0700201", "names": ["dyssomnia", "Dyssomnia", "dyssomnias", "Dyssomnias", "Sleep problem", "sleep problem", "Dyssomnia NOS", "Dyssomnia, NOS", "Sleep problems", "Sleep disturbance", "sleep disturbance", "Dyssomnia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dyssomnias", "shortest_name_length": 9}
{"curie": "MONDO:0033281", "names": ["PKD5", "POLYCYSTIC KIDNEY DISEASE 5", "polycystic kidney disease 5", "DZIP1L polycystic kidney disease", "polycystic kidney disease caused by mutation in DZIP1L"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polycystic kidney disease 5", "shortest_name_length": 4}
{"curie": "MONDO:0003640", "names": ["Histiocytosis Y", "Verruciform Xanthoma", "verruciform xanthoma", "Verruciform xanthoma", "Xanthoma, verruciform", "Skin Verruciform Xanthoma", "skin verruciform xanthoma", "Verruciform xanthoma of skin", "verruciform xanthoma of skin", "Verruciform Xanthoma of Skin", "Cutaneous Verruciform Xanthoma", "cutaneous verruciform xanthoma", "verruciform xanthoma of the skin", "Verruciform Xanthoma of the Skin", "Verruciform xanthoma of skin (disorder)", "Verruciform xanthoma (morphologic abnormality)", "verruciform xanthoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "verruciform xanthoma of skin", "shortest_name_length": 15}
{"curie": "UMLS:C4287998", "names": ["Vulvar Yolk Sac Tumor", "Vulvar Endodermal Sinus Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Yolk Sac Tumor", "shortest_name_length": 21}
{"curie": "MONDO:0014895", "names": ["DEE40", "EIEE40", "early infantile epileptic encephalopathy 40", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 40", "epileptic encephalopathy, early infantile, 40", "GUF1 early infantile epileptic encephalopathy", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 40", "developmental and epileptic encephalopathy 40", "developmental and epileptic encephalopathy, 40", "epileptic encephalopathy, early infantile, type 40", "epileptic encephalopathy, early infantile, 40; EIEE40", "early infantile epileptic encephalopathy caused by mutation in GUF1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 40", "shortest_name_length": 5}
{"curie": "UMLS:C3899187", "names": ["Present", "Extranodal Extension", "Extranodal Involvement", "Extracapsular Extension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extranodal Extension", "shortest_name_length": 7}
{"curie": "MONDO:0800123", "names": ["BPIP", "bronchiolocentric pattern of interstitial pneumonia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bronchiolocentric pattern of interstitial pneumonia", "shortest_name_length": 4}
{"curie": "UMLS:C1332153", "names": ["AML/MDS", "Acute Myeloid Leukemia Arising from Previous Myelodysplastic Syndrome", "Acute Myeloid Leukemia (AML) Arising from Previous Myelodysplastic Syndrome", "Acute Myeloid Leukemia with Multilineage Dysplasia following Myelodysplastic Syndrome", "acute myeloid leukemia with multilineage dysplasia following myelodysplastic syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Myeloid Leukemia Arising from Previous Myelodysplastic Syndrome", "shortest_name_length": 7}
{"curie": "MONDO:0033363", "names": ["DEE54", "EIEE54", "early infantile epileptic encephalopathy 54", "developmental and epileptic encephalopathy 54", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 54", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 54", "epileptic encephalopathy, early infantile, 54", "developmental and epileptic encephalopathy, 54"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 54", "shortest_name_length": 5}
{"curie": "MONDO:0001036", "names": ["hypopyon", "HYPOPYON", "Hypopyon", "Hypopyon (disorder)", "hypopyon (diagnosis)", "iridocyclitis hypopyon", "uveal tract - hypopyon", "hypopyon; iridocyclitis", "Pus in anterior chamber", "iridocyclitis; hypopyon", "anterior chamber hypopyon", "anterior chamber hypopyon (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypopyon", "shortest_name_length": 8}
{"curie": "MONDO:0001052", "names": ["chronic otomycosis", "otomycosis, chronic", "Chronic fungal otitis externa", "chronic fungal otitis externa", "Chronic mycotic otitis externa", "chronic mycotic otitis externa", "Chronic mycotic otitis externa (disorder)", "chronic mycotic otitis externa (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic fungal otitis externa", "shortest_name_length": 18}
{"curie": "MONDO:0006164", "names": ["Colorectal SSA", "colorectal SSP", "Colorectal SSP", "colorectal SSA", "colorectal SSA/P", "Colorectal SSA/P", "colorectal sessile serrated polyp", "Colorectal Sessile Serrated Polyp", "Colorectal Sessile Serrated Adenoma", "colorectal sessile serrated adenoma", "Colorectal Serrated Lesions and Polyps", "Colorectal Sessile Serrated Adenoma/Polyp", "colorectal sessile serrated adenoma/polyp", "Colorectal Mixed Hyperplastic Adenomatous Polyp", "colorectal mixed hyperplastic adenomatous polyp", "colorectal mixed hyperplastic adenomatous polyp/serrated adenoma", "Colorectal Mixed Hyperplastic Adenomatous Polyp/Serrated Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorectal sessile serrated adenoma/polyp", "shortest_name_length": 14}
{"curie": "MONDO:0000030", "names": ["epilepsy, nocturnal frontal lobe", "sleep-related hypermotor epilepsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sleep-related hypermotor epilepsy", "shortest_name_length": 32}
{"curie": "MONDO:0011579", "names": ["LORD", "pigmentary retinopathy", "LATE-ONSET RETINAL DEGENERATION", "Late-onset retinal degeneration", "Late-Onset Retinal Degeneration", "late-onset retinal degeneration", "autosomal dominant late-onset retinal degeneration", "Autosomal dominant late-onset retinal degeneration", "retinal Degeneration, late-onset, autosomal dominant", "RETINAL DEGENERATION, LATE-ONSET, AUTOSOMAL DOMINANT", "Retinal Degeneration, Late-Onset, Autosomal Dominant", "Autosomal dominant late-onset retinal degeneration (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "late-onset retinal degeneration", "shortest_name_length": 4}
{"curie": "MONDO:0009838", "names": ["Parana hard skin syndrome", "Parana Hard Skin Syndrome", "PARANA HARD-SKIN SYNDROME", "Parana Hard-Skin Syndrome", "Parana hard-skin syndrome", "Hard skin syndrome Parana type", "hard skin syndrome Parana type", "Hard Skin Syndrome Parana Type", "hard-skin syndrome, Parana type", "hard skin syndrome, Parana type", "Hard skin syndrome, Parana type", "Parana hard skin syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parana hard-skin syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0011659", "names": ["HTX3", "Heterotaxy, Visceral, 3, Autosomal", "HETEROTAXY, VISCERAL, 3, AUTOSOMAL", "heterotaxy, visceral, 3, autosomal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heterotaxy, visceral, 3, autosomal", "shortest_name_length": 4}
{"curie": "MONDO:0003554", "names": ["colon adenosquamous cancer", "Colon Adenosquamous Cancer", "adenosquamous colon carcinoma", "Colon Adenosquamous Carcinoma", "colon adenosquamous carcinoma", "Adenosquamous Colon Carcinoma", "Colonic Adenosquamous carcinoma", "colonic adenosquamous carcinoma", "Colonic Adenosquamous Carcinoma", "adenosquamous carcinoma of colon", "Adenosquamous Carcinoma of Colon", "Adenosquamous Carcinoma of the Colon", "adenosquamous carcinoma of the colon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenosquamous colon carcinoma", "shortest_name_length": 26}
{"curie": "UMLS:C0220611", "names": ["Rhabdomyosarcoma", "Rhabdomyosarcoma, child", "childhood rhabdomyosarcoma", "Childhood Rhabdomyosarcoma", "pediatric rhabdomyosarcoma", "Pediatric Rhabdomyosarcoma", "rhabdomyosarcoma, childhood", "sarcoma, childhood rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Rhabdomyosarcoma", "shortest_name_length": 16}
{"curie": "MONDO:0016310", "names": ["Niemann-Pick disease type C, adult neurologic onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Niemann-Pick disease type C, adult neurologic onset", "shortest_name_length": 51}
{"curie": "MONDO:0019857", "names": ["Congenital hypothyroidism due to transplacental passage of TSH-binding inhibitory antibodies", "congenital hypothyroidism due to transplacental passage of maternal TSH-binding inhibitory antibodies", "Congenital hypothyroidism due to transplacental passage of maternal thyroid stimulating hormone binding inhibitory antibody", "Congenital hypothyroidism due to transplacental passage of maternal TSH (thyroid stimulating hormone)-binding inhibitory antibody", "Congenital hypothyroidism due to transplacental passage of maternal thyroid stimulating hormone binding inhibitory antibody (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital hypothyroidism due to transplacental passage of maternal TSH-binding inhibitory antibodies", "shortest_name_length": 92}
{"curie": "UMLS:C0750969", "names": ["Vasogenic Brain Edema", "Edema, Vasogenic Brain", "Brain Edema, Vasogenic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vasogenic Brain Edema", "shortest_name_length": 21}
{"curie": "MONDO:0007975", "names": ["MERALGIA PARAESTHETICA, FAMILIAL", "Meralgia Paraesthetica, Familial", "meralgia paraesthetica, familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "meralgia paraesthetica, familial", "shortest_name_length": 32}
{"curie": "UMLS:C4684871", "names": ["Refractory Rhabdoid Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Rhabdoid Tumor", "shortest_name_length": 25}
{"curie": "UMLS:C0855057", "names": ["Primary leiomyosarcoma", "Localized Leiomyosarcoma", "Leiomyosarcoma Nonmetastatic", "Non-Metastatic Leiomyosarcoma", "Leiomyosarcoma non-metastatic", "Primary leiomyosarcoma (disorder)", "Primary leiomyosarcoma (diagnosis)", "malignant neoplasm myosarcoma leiomyosarcoma primary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary leiomyosarcoma", "shortest_name_length": 22}
{"curie": "MONDO:0015498", "names": ["oromandibular-limb anomalies syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oromandibular-limb anomalies syndrome", "shortest_name_length": 37}
{"curie": "MONDO:0001338", "names": ["acute apical periodontitis", "Acute apical periodontitis", "Acute apical periodontitis NOS", "Acute periapical periodontitis", "AAP - acute apical periodontitis", "Acute periradicular periodontitis", "Symptomatic periapical periodontitis", "acute apical periodontitis of pulpal origin", "Acute apical periodontitis of pulpal origin", "Symptomatic periapical periodontitis (disorder)", "acute apical periodontitis of pulpal origin (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute apical periodontitis", "shortest_name_length": 26}
{"curie": "MONDO:0006614", "names": ["Wilkinson-Sneddon", "Sneddon-Wilkinson", "Pustulosis subcornealis", "pustulosis subcornealis", "Sneddon Wilkinson Disease", "Sneddon-Wilkinson disease", "Sneddon-Wilkerson disease", "sneddon wilkinson disease", "Sneddon-Wilkinson Disease", "sneddon-wilkinson disease", "sneddon-wilkinson syndrome", "Sneddon-Wilkinson syndrome", "eczema; pustular subcorneal", "eczema; subcorneal pustular", "pustular; eczema, subcorneal", "Subcorneal pustular dermatosis", "Subcorneal pustular dermatitis", "subcorneal pustular dermatosis", "Sneddon and Wilkinson syndrome", "subcorneal pustular dermatitis", "Subcorneal Pustular Dermatosis", "Subcorneal Pustular Dermatoses", "Pustular Dermatoses, Subcorneal", "Pustular Dermatosis, Subcorneal", "Dermatosis, Subcorneal Pustular", "Dermatoses, Subcorneal Pustular", "pustular; subcorneal dermatitis", "Sneddon-Wilkinson disease or syndrome", "Subcorneal pustular dermatosis (disorder)", "subcorneal pustular dermatosis (diagnosis)", "subcorneal pustular dermatitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subcorneal pustular dermatosis", "shortest_name_length": 17}
{"curie": "MONDO:0030013", "names": ["IMD66", "immunodeficiency 66", "IMMUNODEFICIENCY 66"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 66", "shortest_name_length": 5}
{"curie": "UMLS:C0740832", "names": ["AIDS END STAGE", "end stage AIDS", "End stage AIDS", "AIDS end stages"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "End stage AIDS", "shortest_name_length": 14}
{"curie": "UMLS:C1517125", "names": ["Fallopian Tube Serous Tumor", "Fallopian Tube Serous Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fallopian Tube Serous Neoplasm", "shortest_name_length": 27}
{"curie": "UMLS:C1333954", "names": ["Helicobacter Pylori-Related Non-Hodgkin Lymphoma", "Helicobacter Pylori-Related Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Helicobacter Pylori-Related Non-Hodgkin Lymphoma", "shortest_name_length": 48}
{"curie": "UMLS:C4287840", "names": ["Pre-XDR-TB", "Pre-Extensively Drug-Resistant TB", "Pre-Extensively Drug-Resistant Tuberculosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pre-Extensively Drug-Resistant Tuberculosis", "shortest_name_length": 10}
{"curie": "MONDO:0006836", "names": ["listeria meningitis", "LISTERIA MENINGITIS", "meningitis listeria", "Listeria cerebritis", "Listeria meningitis", "Meningitis listeria", "Listeria Meningitis", "cerebritis, Listeria", "MENINGITIS, LISTERIA", "Meningitis, Listeria", "Listeria Meningitides", "Listeria Cerebritides", "Meningitides, Listeria", "Cerebritides, Listeria", "Listeria meningoencephalitis", "meningoencephalitis, Listeria", "Meningitis due to listeriosis", "Listeria Meningoencephalitides", "Listeria meningitis (disorder)", "Meningoencephalitides, Listeria", "Listeria monocytogenes Meningitis", "Listeria monocytogenes meningitis", "MENINGITIS LISTERIA MONOCYTOGENES", "meningitis, Listeria monocytogenes", "Meningitis, Listeria monocytogenes", "Listeria monocytogenes Meningitides", "Meningitides, Listeria monocytogenes", "listeriosis with meningeal involvement", "Listeria monocytogenes infectious meningitis", "listeriosis with meningeal involvement (diagnosis)", "Listeria monocytogenes caused infectious meningitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Listeria meningitis", "shortest_name_length": 19}
{"curie": "UMLS:C0279915", "names": ["stage I childhood HD", "childhood HD, stage I", "pediatric HD, stage I", "HD, stage I, childhood", "HD, childhood, stage I", "Stage I Hodgkin Lymphoma", "stage I childhood Hodgkin lymphoma", "Stage I Childhood Hodgkin Lymphoma", "stage I childhood Hodgkin's disease", "Pediatric Hodgkin's Disease Stage I", "Childhood Hodgkin's Disease Stage I", "stage I pediatric Hodgkin's disease", "Stage I Childhood Hodgkin's Disease", "Stage I Pediatric Hodgkin's Disease", "pediatric Hodgkin's disease, stage I", "Pediatric Hodgkin's Lymphoma Stage I", "Stage I Childhood Hodgkin's Lymphoma", "Stage I Pediatric Hodgkin's Lymphoma", "Childhood Hodgkin's Lymphoma Stage I", "stage I Hodgkin's disease, childhood", "Hodgkin's disease, childhood, stage I", "childhood Hodgkin's lymphoma, stage I", "lymphoma, stage I childhood Hodgkin's", "Hodgkin's lymphoma, stage I, childhood", "Ann Arbor Stage I Childhood Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Childhood Hodgkin Lymphoma", "shortest_name_length": 20}
{"curie": "UMLS:C3203622", "names": ["Crystal nephropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Crystal nephropathy", "shortest_name_length": 19}
{"curie": "MONDO:0018379", "names": ["primary AVN", "primary avascular necrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary avascular necrosis", "shortest_name_length": 11}
{"curie": "UMLS:C0005943", "names": ["Infectious Bone Disease", "Infectious Bone Diseases", "Bone Disease, Infectious", "Disease, Infectious Bone", "infectious bone diseases", "bone diseases infectious", "Diseases, Infectious Bone", "Bone Diseases, Infectious"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone Diseases, Infectious", "shortest_name_length": 23}
{"curie": "MONDO:0017802", "names": ["Ovarian fibrothecoma", "ovarian fibrothecoma", "Fibrothecoma of ovary", "Fibrothecoma of ovary (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian fibrothecoma", "shortest_name_length": 20}
{"curie": "UMLS:C1336461", "names": ["Stage I Lip Cancer", "Stage I Cancer of Lip", "Stage I Lip Carcinoma", "Stage I Carcinoma of Lip", "Stage I Cancer of the Lip", "Stage I Lip Cancer AJCC v7", "Stage I Lip Cancer AJCC v6", "Stage I Carcinoma of the Lip", "Stage I Lip Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Lip Carcinoma", "shortest_name_length": 18}
{"curie": "MONDO:0011231", "names": ["FEB2", "EIG17", "GEFSP11", "GEFS+11", "GEFS+, TYPE 11", "familial febrile seizures 2", "FEBRILE SEIZURES, FAMILIAL, 2", "febrile seizures, familial, 2", "Seizures, Familial Febrile, 2", "familial febrile convulsions 2", "Febrile Convulsions, Familial, 2", "CONVULSIONS, FAMILIAL FEBRILE, 2", "Convulsions, Familial Febrile, 2", "convulsions, familial febrile, 2", "FEBRILE CONVULSIONS, FAMILIAL, 2 (disorder)", "EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 17", "epilepsy, idiopathic generalized, susceptibility to, 17", "generalized epilepsy with febrile seizures plus, type 11", "GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "febrile seizures, familial, 2", "shortest_name_length": 4}
{"curie": "MONDO:0000568", "names": ["neuroinflammatory disorder\"@e", "central nervous system autoimmune disease", "autoimmune disease of central nervous system", "autoimmune disorder of central nervous system", "central nervous system hypersensitivity reaction type II disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune disorder of central nervous system", "shortest_name_length": 29}
{"curie": "MONDO:0005140", "names": ["Ovarian Cancer", "ovarian cancer", "ovary carcinoma", "Ovarian Carcinoma", "Ovarian carcinoma", "ovarian carcinoma", "carcinoma ovarian", "Carcinoma of Ovary", "carcinoma of ovary", "carcinoma, ovarian", "Carcinoma of the Ovary", "carcinoma of the ovary", "Ovarian Epithelial Cancer", "ovarian epithelial cancer", "cancer epithelial ovarian", "Ovarian epithelial cancer", "epithelial ovarian cancer", "Epithelial Ovarian Cancer", "ovarian cancer epithelial", "Ovarian Cancer, Epithelial", "Cancer, Epithelial Ovarian", "Epithelial Ovarian Cancers", "Ovarian Epithelial Cancers", "Epithelial Cancer, Ovarian", "Cancer, Ovarian Epithelial", "ovarian epithelial carcinoma", "Epithelial Ovarian Carcinoma", "epithelial ovarian carcinoma", "Ovarian Epithelial Carcinoma", "carcinoma, ovarian epithelial", "Epithelial Carcinoma, Ovarian", "Carcinoma, Ovarian Epithelial", "Ovarian Carcinoma, Epithelial", "Carcinoma, Epithelial Ovarian", "Ovarian Epithelial Carcinomas", "Epithelial Ovarian Carcinomas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian carcinoma", "shortest_name_length": 14}
{"curie": "MONDO:0008978", "names": ["CHDM", "chordoma", "Chordoma", "chordomas", "Chordomas", "notochordoma", "Chordoma, NOS", "chordoma (disease)", "Notochordal sarcoma", "CHORDOMA, MALIGNANT", "Chordoma (disorder)", "chordoma, malignant", "notochordal sarcoma", "chordoma (diagnosis)", "susceptibility to chordoma", "CHORDOMA, SUSCEPTIBILITY TO", "chordoma, susceptibility to", "Chordoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chordoma", "shortest_name_length": 4}
{"curie": "UMLS:C3203531", "names": ["Post-traumatic neck syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post-traumatic neck syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0005956", "names": ["Black Death", "Black Plague", "Plague sepsis", "septic; plague", "septicemic plague", "Septicemic plague", "SEPTICEMIC PLAGUE", "Septicemic Plague", "septicemic; plague", "Septicaemic plague", "plague; septicemic", "Yersinia pestis; sepsis", "sepsis; Yersinia pestis", "Septicemic plague (disorder)", "septicemic plague (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "septicemic plague", "shortest_name_length": 11}
{"curie": "MONDO:0012811", "names": ["ANIB8", "intracranial berry aneurysm 8", "aneurysm, intracranial berry, 8", "Aneurysm, Intracranial Berry, 8", "ANEURYSM, INTRACRANIAL BERRY, 8", "aneurysm, intracranial BERRY, 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aneurysm, intracranial berry, 8", "shortest_name_length": 5}
{"curie": "MONDO:0001270", "names": ["Stone in bladder diverticulum", "stone in bladder diverticulum", "bladder; diverticular calculus", "calculus; bladder diverticulum", "diverticulum; calculus, bladder", "calculus; diverticulum, bladder", "Calculus of bladder diverticulum", "bladder; calculus in diverticulum", "Calculus in diverticulum of bladder", "calculus in diverticulum of bladder", "diverticulum; bladder, with calculus", "Diverticulum of bladder with calculus", "Calculus in diverticulum of bladder (disorder)", "calculus in diverticulum of bladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stone in bladder diverticulum", "shortest_name_length": 29}
{"curie": "UMLS:C0340758", "names": ["Superior vena cava stenosis", "Superior Vena Cava Stenosis", "Superior vena cava stenosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Superior vena cava stenosis", "shortest_name_length": 27}
{"curie": "MONDO:0700170", "names": ["equine neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "equine neoplasm", "shortest_name_length": 15}
{"curie": "MONDO:0016858", "names": ["blepharophimosis types 1 and 2 due to a point mutation", "blepharophimosis-epicanthus inversus-ptosis due to a point mutation syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blepharophimosis-epicanthus inversus-ptosis due to a point mutation syndrome", "shortest_name_length": 54}
{"curie": "MONDO:0014479", "names": ["POROK8", "porokeratosis 8, disseminated superficial actinic type", "POROKERATOSIS 8, DISSEMINATED SUPERFICIAL ACTINIC TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "porokeratosis 8, disseminated superficial actinic type", "shortest_name_length": 6}
{"curie": "MONDO:0004957", "names": ["CEMU", "Mucous Carcinoma", "mucous carcinoma", "Mucoid carcinoma", "mucoid carcinoma", "Mucoid Carcinoma", "Mucous carcinoma", "Colloid Carcinoma", "colloid carcinoma", "Colloid carcinoma", "mucinous carcinoma", "Mucinous carcinoma", "Mucinous Carcinoma", "Colloid Carcinomas", "mucinuos carcinoma", "Carcinoma, Colloid", "Mucinous Carcinomas", "Carcinoma, Mucinous", "Carcinomas, Colloid", "Gelatinous Carcinoma", "Carcinomas, Mucinous", "gelatinous carcinoma", "Gelatinous carcinoma", "Mucoid adenocarcinoma", "Mucous Adenocarcinoma", "Mucoid Adenocarcinoma", "Mucous adenocarcinoma", "mucous adenocarcinoma", "mucoid adenocarcinoma", "adenocarcinoma mucous", "Colloid adenocarcinoma", "colloid adenocarcinoma", "Colloid Adenocarcinoma", "Mucinous adenocarcinoma", "mucinous adenocarcinoma", "ADENOCARCINOMA MUCINOUS", "adenocarcinoma mucinous", "Mucinous Adenocarcinoma", "Mucinous Adenocarcinomas", "Adenocarcinoma, Mucinous", "Mucin-Producing Carcinoma", "carcinoma mucin secreting", "Adenocarcinomas, Mucinous", "Gelatinous adenocarcinoma", "mucin-secreting carcinoma", "gelatinous adenocarcinoma", "Mucin-secreting carcinoma", "Mucin-Secreting carcinoma", "Mucin-producing carcinoma", "Gelatinous Adenocarcinoma", "Mucin-Producing Adenocarcinoma", "Mucin-producing adenocarcinoma", "Mucin-Secreting adenocarcinoma", "mucin-producing adenocarcinoma", "mucin-secreting adenocarcinoma", "Mucin-secreting adenocarcinoma", "adenocarcinoma mucin secreting", "mucinous adenocarcinoma (diagnosis)", "ADENOCARCINOMA, MUCINOUS, MALIGNANT", "adenocarcinoma, mucinous, malignant", "mucin-producing adenocarcinoma (diagnosis)", "pseudomyxoma peritonei with unknown primary site", "Pseudomyxoma peritonei with unknown primary site", "Mucinous adenocarcinoma (morphologic abnormality)", "mucin-producing adenocarcinoma (morphologic abnormality)", "Mucin-producing adenocarcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucinous adenocarcinoma", "shortest_name_length": 4}
{"curie": "UMLS:C5237199", "names": ["Advanced Ovarian Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Ovarian Carcinoma", "shortest_name_length": 26}
{"curie": "UMLS:C0264733", "names": ["Dilated ventricle", "dilated ventricles", "Ventricular dilation", "Ventricular dilatation", "Dilatation ventricular", "Dilatation;ventricular", "ventricular dilatation", "dilatation; ventricular", "ventricular; dilatation", "Cardiac ventricular dilatation", "Dilatation of cardiac ventricle", "Ventricular dilatation (disorder)", "Dilatation of cardiac ventricle (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ventricular dilatation (disorder)", "shortest_name_length": 17}
{"curie": "UMLS:C0920235", "names": ["Psoriatic plaque"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Psoriatic plaque", "shortest_name_length": 16}
{"curie": "MONDO:0005396", "names": ["aneurysm thoracic", "thoracic aneurysm", "aneurysms thoracic", "ANEURYSM, THORACIC", "intrathoracic aneurysm", "Aneurysm;intrathoracic", "Thoracic Aorta Aneurysm", "intrathoracic; aneurysm", "thoracic aorta aneurysm", "AORTA THORACIC ANEURYSM", "aneurysm; intrathoracic", "aorta thoracic; aneurysm", "aneurysm aortic thoracic", "Aorta Aneurysm, Thoracic", "Thoracic Aortic Aneurysm", "Thoracic aortic aneurysm", "aortic aneurysm thoracic", "aortic thoracic aneurysm", "Thoracic Aorta Aneurysms", "thoracic aortic aneurysm", "aneurysm; thoracic aorta", "Aneurysm, Thoracic Aorta", "Aortic Aneurysm, Thoracic", "thoracic aortic aneurysms", "ANEURYSM, THORACIC AORTIC", "Ectasia of thoracic aorta", "ANEURYSM, AORTA, THORACIC", "Aneurysm, Thoracic Aortic", "Thoracic Aortic Aneurysms", "Aneurysm of thoracic aorta", "aneurysm of thoracic aorta", "Dilatation of thoracic aorta", "Dilatation of the thoracic aorta", "Ectasia of thoracic aorta (disorder)", "Aneurysm of thoracic aorta (disorder)", "aneurysm of thoracic aorta (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thoracic aortic aneurysm", "shortest_name_length": 17}
{"curie": "MONDO:0014475", "names": ["SCA40", "spinocerebellar ataxia 40", "SPINOCEREBELLAR ATAXIA 40", "Spinocerebellar ataxia type 40", "spinocerebellar ataxia type 40", "Spinocerebellar ataxia type 40 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia type 40", "shortest_name_length": 5}
{"curie": "MONDO:0001332", "names": ["Hench's syndrome", "palindromic rheumatism", "Palindromic rheumatism", "Palindromic Rheumatism", "palindromic; rheumatism", "Rheumatism, palindromic", "rheumatism; palindromic", "RHEUMATISM, PALINDROMIC", "Hench-Rosenberg syndrome", "intermittent hydrarthrosis", "Palindromic rheumatism syndrome", "Palindromic rheumatism (disorder)", "palindromic rheumatism (diagnosis)", "intermittent hydrarthrosis of shoulder", "Palindromic rheumatism, shoulder region", "Palindromic rheumatism, site unspecified", "Palindromic rheumatism, unspecified site", "Palindromic rheumatism of shoulder region", "palindromic rheumatism of the shoulder region", "Palindromic rheumatism of the shoulder region", "Palindromic rheumatism involving shoulder region", "Palindromic rheumatism of shoulder region (disorder)", "palindromic rheumatism of the shoulder region (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "palindromic rheumatism", "shortest_name_length": 16}
{"curie": "UMLS:C1709611", "names": ["Postradiation Osteosarcoma", "Radiation-Related Osteosarcoma", "Radiation-Associated Osteosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radiation-Related Osteosarcoma", "shortest_name_length": 26}
{"curie": "MONDO:0006757", "names": ["Cholestasis extrahepatic", "extrahepatic cholestasis", "Extrahepatic Cholestasis", "Extrahepatic cholestasis", "cholestasis extrahepatic", "Cholestasis, Extrahepatic", "extrahepatic biliary Stasis", "extrahepatic biliary stasis", "Extrahepatic Biliary Stasis", "Biliary Stasis, Extrahepatic", "extrahepatic biliary obstruction", "BILIARY OBSTRUCTION EXTRAHEPATIC", "Extrahepatic biliary obstruction", "extrahepatic cholestasis (finding)", "extrahepatic bile duct cholestasis", "Extrahepatic Bile Duct Obstruction", "Extrahepatic cholestasis (finding)", "Bile Duct Obstruction, Extrahepatic", "cholestasis of extrahepatic bile duct", "extrahepatic obstructive biliary disease", "Extrahepatic obstructive biliary disease", "extrahepatic biliary obstruction (diagnosis)", "Extrahepatic obstructive biliary disease (disorder)", "extrahepatic obstructive biliary disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extrahepatic cholestasis", "shortest_name_length": 24}
{"curie": "MONDO:0004131", "names": ["Anal Verrucous Carcinoma", "anal verrucous carcinoma", "anal Buschke-Lowenstein tumor", "Anal Buschke-Lowenstein Tumor", "anal Giant (malignant) Condyloma", "anal giant (malignant) condyloma", "Anal Giant (Malignant) Condyloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anal verrucous carcinoma", "shortest_name_length": 24}
{"curie": "UMLS:C0156308", "names": ["edema penis", "PENIS EDEMA", "PENILE EDEMA", "edema; penis", "Penile edema", "penile edema", "penis; edema", "Penile oedema", "edema of penis", "Edema of penis", "Edematous penis", "Oedema of penis", "penis swelling edema", "Edema of penis (disorder)", "edema of penis (diagnosis)", "penile edema (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Edema of penis", "shortest_name_length": 11}
{"curie": "MONDO:0002060", "names": ["Duct Adenoma", "duct adenoma", "Duct adenoma", "duct papilloma", "ductal papilloma", "Ductal papilloma", "Ductal Papilloma", "Duct adenoma, NOS", "ductal papillomas", "Intraductal papilloma", "papilloma intraductal", "intraductal papilloma", "Intraductal Papilloma", "Intraductal Papillomas", "Papilloma, Intraductal", "intraductal papillomas", "Papillomas, Intraductal", "Intraductal papilloma (morphologic abnormality)", "intraductal papilloma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intraductal papilloma", "shortest_name_length": 12}
{"curie": "UMLS:C5419084", "names": ["Locally Advanced Ampulla of Vater Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Ampulla of Vater Carcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0012855", "names": ["JBTS8", "Joubert syndrome 8", "JOUBERT SYNDROME 8", "Joubert Syndrome 8", "Joubert syndrome type 8", "ARL13B Joubert syndrome", "JOUBERT SYNDROME 8 (disorder)", "Joubert syndrome caused by mutation in ARL13B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome 8", "shortest_name_length": 5}
{"curie": "UMLS:C1333795", "names": ["Crohn's Associated Gastritis", "Gastritis Associated with Crohn Disease", "Gastritis Associated with Crohn's Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastritis Associated with Crohn Disease", "shortest_name_length": 28}
{"curie": "UMLS:C0877355", "names": ["Localized Gallbladder Cancer", "localized gallbladder cancer", "Gallbladder Cancer, Localized", "Gallbladder carcinoma localized", "Localized Gallbladder Carcinoma", "Gallbladder carcinoma localised", "Localized Cancer of Gallbladder", "Localized Cancer of the Gallbladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized Gallbladder Carcinoma", "shortest_name_length": 28}
{"curie": "UMLS:C0281708", "names": ["Recurrent Burkitt Lymphoma", "Recurrent Childhood Burkitt Lymphoma", "Recurrent Childhood Burkitt's Lymphoma", "relapsed childhood small noncleaved cell lymphoma", "lymphoma, relapsed childhood small noncleaved cell", "recurrent childhood small noncleaved cell lymphoma", "relapsed small noncleaved cell lymphoma, childhood", "pediatric small noncleaved cell lymphoma, relapsed", "childhood small noncleaved cell lymphoma, relapsed", "Relapsed Childhood Small Non-Cleaved Cell Lymphoma", "Relapsed Pediatric Small Non-Cleaved Cell Lymphoma", "Recurrent Pediatric Small Non-Cleaved Cell Lymphoma", "small noncleaved cell lymphoma, childhood, relapsed", "lymphoma, recurrent childhood small noncleaved cell", "recurrent small noncleaved cell lymphoma, childhood", "Recurrent Childhood Small Non-Cleaved Cell Lymphoma", "small noncleaved cell lymphoma, childhood, recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Burkitt Lymphoma", "shortest_name_length": 26}
{"curie": "MONDO:0020128", "names": ["Motor System Disease", "Disease;motor neuron", "MOTOR SYSTEM DISEASE", "Motor Neuron Disease", "disease motor neuron", "MOTOR NEURON DISEASE", "Motor neuron disease", "motor neuron disease", "disease motor neurons", "disease motor neurone", "MOTOR NEURON DISEASES", "Neuron Disease, Motor", "Motor Neuron Diseases", "motor neuron disorder", "Motor System Diseases", "motor neurone disease", "motor neuron diseases", "Motor neurone disease", "Neuron Diseases, Motor", "disease motor neurones", "Motor neurone diseases", "disease of motor neuron", "Motor neurons--Diseases", "disorder of motor neuron", "Motor neuron disease, NOS", "ANTERIOR HORN CELL DISEASE", "Anterior Horn Cell Disease", "Anterior horn cell disease", "anterior horn cell disease", "anterior cell diseases horn", "MND - Motor neurone disease", "anterior horn cell; disorder", "Anterior horn cell disease NOS", "Motor neuron disease (disorder)", "Anterior horn cell disease, NOS", "motor neuron disease (diagnosis)", "Motor neuron disease or syndrome", "motor neuron disease or disorder", "Motor neuron disease, unspecified", "degenerative motor system disease", "Anomaly of the anterior horn cells", "degenerative motor system disorder", "disease or disorder of motor neuron", "Motor Neuron Diseases and Syndromes", "Anterior horn cell disease (disorder)", "Abnormality of the anterior horn cell", "Abnormal anterior horn cell morphology", "Unspecified anterior horn cell disease", "Abnormality of the anterior horn cells", "Anterior horn cell disease, unspecified", "disease (or disorder); anterior horn cell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "motor neuron disorder", "shortest_name_length": 20}
{"curie": "MONDO:0015343", "names": ["secondary acute transverse myelitis", "disease-associated transverse myelitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary acute transverse myelitis", "shortest_name_length": 35}
{"curie": "MONDO:0021333", "names": ["Lip Cancer", "lip cancer", "lip carcinoma", "Lip Carcinoma", "carcinoma lip", "carcinomas lip", "CARCINOMA OF LIP", "Carcinoma of lip", "Carcinoma of Lip", "carcinoma of lip", "Carcinoma of the Lip", "carcinoma of the Lip", "Carcinoma of lip (disorder)", "carcinoma of lip (diagnosis)", "lip neoplasm malignant carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma of lip", "shortest_name_length": 10}
{"curie": "UMLS:C0948561", "names": ["Gynecological chlamydia infection", "Gynaecological chlamydia infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gynecological chlamydia infection", "shortest_name_length": 33}
{"curie": "UMLS:C0349719", "names": ["Scrum pox", "Herpes simplex infection of skin", "herpes simplex infection of skin", "Cutaneous herpes simplex infection", "Herpes simplex infection of skin (disorder)", "herpes simplex infection of skin (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Herpes simplex infection of skin", "shortest_name_length": 9}
{"curie": "UMLS:C3494405", "names": ["Maternal Death", "Maternal death", "Maternal Deaths", "Death, Maternal", "Deaths, Maternal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Maternal Death", "shortest_name_length": 14}
{"curie": "MONDO:0018600", "names": ["congenital CNVI palsy", "congenital abducens nerve palsy", "benign congenital sixth cranial nerve palsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital abducens nerve palsy", "shortest_name_length": 21}
{"curie": "UMLS:C0340517", "names": ["atrial thrombus", "Atrial Thrombus", "ATRIAL THROMBUS", "Atrial thrombosis", "atrial thrombosis", "Thrombus of atrium", "atrium; thrombosis", "thrombosis; atrial", "thrombosis; auricular", "auricular; thrombosis", "Thrombus of atrium (disorder)", "atrial thrombosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atrial thrombosis", "shortest_name_length": 15}
{"curie": "MONDO:0009636", "names": ["MTDPS3", "deoxyguanosine kinase deficiency", "mitochondrial DNA depletion syndrome 3", "MITOCHONDRIAL DNA DEPLETION SYNDROME 3", "DGUOK mitochondrial DNA depletion syndrome", "mitochondrial DNA depletion syndrome type 3", "MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)", "mitochondrial DNA depletion syndrome 3 (hepatocerebral type)", "mitochondrial DNA depletion syndrome caused by mutation in DGUOK", "Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency", "mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency", "Mitochondrial deoxyribonucleic acid depletion syndrome, hepatocerebral form due to deoxyguanosine kinase deficiency", "Mitochondrial deoxyribonucleic acid depletion syndrome, hepatocerebral form due to deoxyguanosine kinase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial DNA depletion syndrome 3 (hepatocerebral type)", "shortest_name_length": 6}
{"curie": "MONDO:0007595", "names": ["MCFD4", "FMFD IV", "multiple coagulation Factor deficiency 4", "Multiple Coagulation Factor Deficiency IV", "MULTIPLE COAGULATION FACTOR DEFICIENCY IV", "Factor VII and Factor VIII, Combined Deficiency", "factor 7 and Factor VIII, combined deficiency of", "familial multiple coagulation Factor deficiency 4", "FACTOR VII AND FACTOR VIII, COMBINED DEFICIENCY OF", "Familial Multiple Coagulation Factor Deficiency IV", "factor VII and Factor VIII, combined deficiency of", "FAMILIAL MULTIPLE COAGULATION FACTOR DEFICIENCY IV"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "factor VII and Factor VIII, combined deficiency of", "shortest_name_length": 5}
{"curie": "UMLS:C4054168", "names": ["Port Site Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Port Site Infection", "shortest_name_length": 19}
{"curie": "MONDO:0017051", "names": ["classic MSUD", "classic BCKD deficiency", "classic maple syrup urine disease", "classic branched-chain ketoaciduria", "classic branched-chain 2-ketoacid dehydrogenase deficiency", "classic branched-chain alpha-ketoacid dehydrogenase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "classic maple syrup urine disease", "shortest_name_length": 12}
{"curie": "MONDO:0041536", "names": ["FESLF", "Izumi fever", "Izumi fever (disorder)", "Izumi fever (diagnosis)", "Far-East scarlet-like fever"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Far-East scarlet-like fever", "shortest_name_length": 5}
{"curie": "UMLS:C1285373", "names": ["Disease;respiratory;newborn", "Respiratory disorder neonatal", "Neonatal respiratory disorders", "respiratory; disorder, newborn", "respiratory disease of a newborn", "Respiratory disorder NOS neonatal", "respiratory conditions after birth", "Neonatal Respiratory System Disorder", "Neonatal respiratory system disorder", "disease (or disorder); respiratory, newborn", "respiratory conditions after birth (diagnosis)", "Neonatal respiratory system disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neonatal respiratory system disorder", "shortest_name_length": 27}
{"curie": "MONDO:0015255", "names": ["Jorgenson-Lenz syndrome", "Jorgenson Lenz syndrome", "Blepharophimosis radioulnar synostosis", "blepharophimosis radioulnar synostosis", "blepharophimosis-radioulnar synostosis syndrome", "ptosis, prognathism, microcephaly, radio-ulnar synostosis, short stature/dwarfism", "Ptosis, prognathism, microcephaly, radio-ulnar synostosis, short stature-dwarfism", "mild short stature, microcephaly, ptosis-blepharophimosis, facial asymmetry, and radioulnar synostosis", "Mild short stature, microcephaly, ptosis-blepharophimosis, facial asymmetry, and radioulnar synostosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blepharophimosis-radioulnar synostosis syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0013619", "names": ["NPHS6", "PTPRO nephrotic syndrome", "nephrotic syndrome type 6", "nephrotic syndrome, type 6", "NEPHROTIC SYNDROME, TYPE 6", "nephrotic syndrome caused by mutation in PTPRO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrotic syndrome, type 6", "shortest_name_length": 5}
{"curie": "UMLS:C0242594", "names": ["residual cancer", "Residual Cancer", "Residual Cancers", "Cancer, Residual"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Residual Cancer", "shortest_name_length": 15}
{"curie": "MONDO:0012185", "names": ["SMDA4", "spondylometaphyseal dysplasia A4 type", "spondylometaphyseal dysplasia type A4", "Spondylometaphyseal dysplasia A4 type", "spondylometaphyseal dysplasia, A4 type", "Spondylometaphyseal Dysplasia, Type A4", "SPONDYLOMETAPHYSEAL DYSPLASIA, TYPE A4", "Spondylometaphyseal dysplasia, A4 type", "spondylometaphyseal dysplasia, type A4", "Spondylometaphyseal dysplasia A4 type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondylometaphyseal dysplasia, A4 type", "shortest_name_length": 5}
{"curie": "MONDO:0016557", "names": ["Porcelain nails", "total leukonychia", "Leuconychia totalis", "Leukonychia totalis", "leukonychia totalis", "hereditary white nails", "Hereditary white nails", "leukonychia totalis was seen", "Leukonychia totalis (disorder)", "leukonychia totalis (diagnosis)", "leukonychia totalis (physical finding)", "nails discoloration white (leukonychia) totalis", "anomalies of nails congenital leukonychia totalis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukonychia totalis", "shortest_name_length": 15}
{"curie": "MONDO:0015074", "names": ["THYROID", "THYROID TUMOR", "tumor thyroid", "thyroid tumor", "Thyroid Tumor", "Thyroid tumor", "thyroid tumors", "Thyroid tumour", "thyroid tumour", "Thyroid cancer", "thyroid tumours", "thyroid neoplasm", "Neoplasm thyroid", "neoplasm thyroid", "Thyroid Neoplasm", "tumor of thyroid", "NEOPLASM THYROID", "Tumor of Thyroid", "Thyroid neoplasm", "thyroid neoplasms", "THRYOID NEOPLASIA", "neoplasms thyroid", "Thyroid neoplasms", "Neoplasm, Thyroid", "Thyroid neoplasia", "Thyroid Neoplasms", "Neoplasms, Thyroid", "Neoplasm of Thyroid", "thyroid gland tumor", "neoplasm of thyroid", "Thyroid Gland Tumor", "tumor thyroid gland", "Thyroid neoplasm NOS", "Tumor of the Thyroid", "tumor of the thyroid", "gland thyroid tumors", "Thyroid gland--Tumors", "gland thyroid tumours", "thyroid gland neoplasm", "tumor of thyroid gland", "Tumor of Thyroid Gland", "Tumor of thyroid gland", "Thyroid Gland Neoplasm", "Neoplasm of the Thyroid", "Tumour of thyroid gland", "gland neoplasms thyroid", "neoplasm of the thyroid", "Neoplasm of thyroid gland", "neoplasm of thyroid gland", "Neoplasm of Thyroid Gland", "Tumor of the Thyroid Gland", "tumor of the thyroid gland", "neoplasm of the thyroid gland", "Neoplasm of the Thyroid Gland", "Neoplasm of the thyroid gland", "Neoplasia of the thyroid gland", "thyroid gland neoplasm (disease)", "Neoplasm of thyroid gland (disorder)", "neoplasm of thyroid gland (diagnosis)", "neoplasm located in the thyroid gland", "thyroid neoplasm location: thyroid gland", "thyroid neoplasm location: thyroid gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid tumor", "shortest_name_length": 7}
{"curie": "UMLS:C1142471", "names": ["Central Line Complication", "Central line complication", "central line complication", "central complications line"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central line complication", "shortest_name_length": 25}
{"curie": "UMLS:C1336286", "names": ["Follicular lymphoma stage II", "Stage II Follicular Lymphoma", "Ann Arbor Stage II Follicular Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Follicular lymphoma stage II", "shortest_name_length": 28}
{"curie": "MONDO:0003265", "names": ["Reactive Disorder", "reactive disorder", "adaption; reaction", "adjustment disease", "Reactive Disorders", "disorder, reactive", "Disorder, Reactive", "reaction; adaption", "reaction adjustment", "Adjustment disorder", "adjustment disorder", "adjustment reaction", "Adjustment reaction", "disorders, reactive", "Adjustment Disorder", "adaptation reaction", "Disorder;adjustment", "Disorders, Reactive", "ADJUSTMENT DISORDER", "Adaptation reaction", "Disorder, Adjustment", "Adjustment disorders", "disorder; adjustment", "adjustment disorders", "Adjustment Disorders", "disorder, adjustment", "ADJUSTMENT DISORDERS", "reaction; adjustment", "adjustment reactions", "Disorders, Adjustment", "disorders, adjustment", "Adaptation reaction NOS", "Adjustment reaction NOS", "Adjustment disorder NOS", "Adjustment reaction, NOS", "Adaptation reaction, NOS", "Adjustment disorder, NOS", "disorder; situational, acute", "situational; disorder, acute", "acute situational disturbance", "Acute situational disturbance", "Adjustment disorder (disorder)", "Unspecified adjustment reaction", "disturbance; situational, acute", "adjustment disorder (diagnosis)", "situational; disturbance, acute", "Adjustment reaction, unspecified", "Adjustment disorder, unspecified", "Adjustment disorders, Unspecified", "Transient situational disturbance", "Transient Situational Disturbance", "Disturbance, Transient Situational", "Acute situational disturbance, NOS", "Transient Situational Disturbances", "TRANSIENT SITUATIONAL DISTURBANCES", "Situational Disturbance, Transient", "Situational Disturbances, Transient", "Disturbances, Transient Situational", "Transient situational disturbance, NOS", "Acute situational disturbance syndrome", "Acute situational disturbance (disorder)", "Brief situational non-psychotic disorder", "acute situational disturbance (diagnosis)", "Brief situational non-psychotic disorder, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adjustment disorder", "shortest_name_length": 17}
{"curie": "MONDO:0015406", "names": ["CAMS1", "Cerebrofacial arteriovenous metameric syndrome type 1", "cerebrofacial arteriovenous metameric syndrome type 1", "Cerebrofacial arteriovenous metameric syndrome type 1 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebrofacial arteriovenous metameric syndrome type 1", "shortest_name_length": 5}
{"curie": "MONDO:0003842", "names": ["Cerebellar Astrocytoma", "cerebellar astrocytoma", "cerebellum juvenile astrocytoma", "pediatric cerebellar astrocytoma", "Pediatric Cerebellar Astrocytoma", "Childhood Cerebellar Astrocytoma", "childhood cerebellar astrocytoma", "cerebellar astrocytoma, childhood", "Childhood Astrocytoma of Cerebellum", "Pediatric Astrocytoma of Cerebellum", "pediatric astrocytoma of Cerebellum", "pediatric astrocytoma of cerebellum", "childhood astrocytoma of cerebellum", "cerebellum childhood astrocytic tumor", "Pediatric Astrocytoma of the Cerebellum", "pediatric astrocytoma of the cerebellum", "childhood astrocytoma of the cerebellum", "Childhood Astrocytoma of the Cerebellum", "childhood cerebellar astrocytic neoplasm", "childhood astrocytic tumor of cerebellum", "CNS tumor, pediatric cerebellar astrocytoma", "pediatric CNS tumor, cerebellar astrocytoma", "CNS tumor, childhood cerebellar astrocytoma", "childhood CNS tumor, cerebellar astrocytoma", "brain tumor, pediatric cerebellar astrocytoma", "brain tumor, childhood cerebellar astrocytoma", "pediatric brain tumor, cerebellar astrocytoma", "childhood brain tumor, cerebellar astrocytoma", "central nervous system tumor, cerebellar astrocytoma, childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood cerebellar astrocytic neoplasm", "shortest_name_length": 22}
{"curie": "UMLS:C1707550", "names": ["Cutaneous Mantle Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous Mantle Cell Lymphoma", "shortest_name_length": 30}
{"curie": "MONDO:0009870", "names": ["Pili Torti", "pili torti", "Pili torti", "hair twist", "Twisted hair", "Twisted Hair", "TWISTED HAIR", "twisted hair", "hair twisting", "twisted; hair", "hair; twisted", "pili torti (disease)", "Pili torti (disorder)", "PILI TORTI, EARLY-ONSET", "pili torti, early-onset", "pili torti, Ronchese type", "PILI TORTI, RONCHESE TYPE", "Flattened and twisted hair", "coarse, dry, lusterless hair which breaks off easily"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pili torti", "shortest_name_length": 10}
{"curie": "MONDO:0030732", "names": ["SPGF69", "SPERMATOGENIC FAILURE 69", "spermatogenic failure 69"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 69", "shortest_name_length": 6}
{"curie": "MONDO:0006716", "names": ["THROMBOSIS CORONARY", "Coronary Thromboses", "CORONARY THROMBOSIS", "Coronary thrombosis", "thrombosis coronary", "Coronary Thrombosis", "Thrombosis coronary", "coronary thrombosis", "THROMBOSIS, CORONARY", "Thromboses, Coronary", "Thrombosis, Coronary", "Thrombosis - coronary", "CT - Coronary thrombosis", "coronary artery thrombosis", "Thrombosis;artery;coronary", "Coronary artery thrombosis", "coronary (artery) thrombosis", "Occlusive coronary artery thrombus", "coronary vessel thrombotic disease", "Coronary artery thrombosis (disorder)", "thrombotic disease of coronary vessel", "coronary artery thrombosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coronary thrombosis", "shortest_name_length": 19}
{"curie": "MONDO:0100048", "names": ["GVHDS", "GRAFT-VERSUS-HOST DISEASE, RESISTANCE TO", "graft-versus-host disease, susceptibility to", "GRAFT-VERSUS-HOST DISEASE, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "graft-versus-host disease, susceptibility to", "shortest_name_length": 5}
{"curie": "MONDO:0009586", "names": ["mesangial sclerosis, diffuse renal, with ocular abnormalities", "Mesangial Sclerosis, Diffuse Renal, with Ocular Abnormalities", "MESANGIAL SCLEROSIS, DIFFUSE RENAL, WITH OCULAR ABNORMALITIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mesangial sclerosis, diffuse renal, with ocular abnormalities", "shortest_name_length": 61}
{"curie": "UMLS:C1333794", "names": ["Gastric Villous Adenoma", "villous adenoma of stomach", "Villous Adenoma of Stomach", "benign gastric villous adenoma", "Villous Adenoma of the Stomach", "villous adenoma of stomach (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "villous adenoma of stomach", "shortest_name_length": 23}
{"curie": "UMLS:C0037578", "names": ["Injury;soft tissue", "Soft tissue injury", "Soft Tissue Injury", "SOFT TISSUE INJURY", "soft tissue injury", "injury soft tissue", "Injury, Soft Tissue", "Soft tissue injuries", "injuries soft tissue", "soft tissue injuries", "Soft Tissue Injuries", "injuries soft tissues", "Injuries, Soft Tissue", "Soft tissue injury NOS", "STI - Soft tissue injury", "Soft tissue injury (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Soft Tissue Injuries", "shortest_name_length": 18}
{"curie": "MONDO:0016068", "names": ["fibrochondrogenesis", "Fibrochondrogenesis", "FIBROCHONDROGENESIS", "Fibrochondrogenesis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibrochondrogenesis", "shortest_name_length": 19}
{"curie": "UMLS:C4763797", "names": ["Refractory Aggressive NK-Cell Leukemia", "Refractory Aggressive NK-Cell Leukemia/Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Aggressive NK-Cell Leukemia", "shortest_name_length": 38}
{"curie": "MONDO:0000958", "names": ["Neuroretinitis", "neuroretinitis", "Papilloretinitis", "papilloretinitis", "Neuroretinitis NOS", "Neuroretinitis (disorder)", "neuroretinitis (diagnosis)", "Juxtapapillary focal retinitis AND retinochoroiditis", "Juxtapapillary focal retinitis and retinochoroiditis", "Focal retinitis and retinochoroiditis, juxtapapillary", "focal retinitis and retinochoroiditis, juxtapapillary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuroretinitis", "shortest_name_length": 14}
{"curie": "UMLS:C4054576", "names": ["Malignant Osteoclastic Giant Cell-Rich Tumor of Bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Osteoclastic Giant Cell-Rich Tumor of Bone", "shortest_name_length": 52}
{"curie": "UMLS:C0340950", "names": ["sideropenia", "Sideropenia", "Non-Anemic Iron Deficiency", "Iron deficiency without anemia", "iron deficiency without anemia", "Iron Deficiency without Anemia", "Iron deficiency without anaemia", "Iron deficiency without anemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Iron deficiency without anemia", "shortest_name_length": 11}
{"curie": "UMLS:C0856115", "names": ["Diverticulitis aggravated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diverticulitis aggravated", "shortest_name_length": 25}
{"curie": "UMLS:C0750955", "names": ["Spastic neurogenic bladder", "Spastic Neurogenic Bladder", "Neurogenic Bladder, Spastic", "Spastic neuropathic bladder", "Neurogenic Urinary Bladder, Spastic", "Spastic neurogenic bladder (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neurogenic Urinary Bladder, Spastic", "shortest_name_length": 26}
{"curie": "MONDO:0004091", "names": ["skin basaloid carcinoma", "Skin Basaloid Carcinoma", "skin basaloid squamous cell carcinoma", "Skin Basaloid Squamous Cell Carcinoma", "basaloid skin squamous cell carcinoma", "basaloid squamous cell skin carcinoma", "skin Basaloid squamous cell carcinoma", "Basaloid Skin Squamous Cell Carcinoma", "zone of skin basaloid squamous cell carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin basaloid carcinoma", "shortest_name_length": 23}
{"curie": "UMLS:C0271685", "names": ["Diabetic Amyotrophy", "amyotrophy diabetic", "Diabetic amyotrophy", "diabetic amyotrophy", "Amyotrophy, Diabetic", "Diabetic Amyotrophies", "Amyotrophies, Diabetic", "Diabetic lumbosacral plexopathy", "amyotrophy due to diabetes mellitus", "diabetes; amyotrophy (manifestation)", "amyotrophy; diabetes (manifestation)", "amyotrophy secondary to diabetes mellitus", "Diabetic lumbosacral radiculoplexus neuropathy", "amyotrophy secondary to diabetes mellitus (diagnosis)", "DLRPN - diabetic lumbosacral radiculoplexus neuropathy", "Lumbosacral radiculoplexus neuropathy with diabetes mellitus", "Lumbosacral radiculoplexus neuropathy due to diabetes mellitus", "Lumbosacral radiculoplexus neuropathy due to diabetes mellitus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diabetic Amyotrophy", "shortest_name_length": 19}
{"curie": "MONDO:0002193", "names": ["Bartholin gland neoplasm", "tumor of Bartholin's gland", "Benign Bartholin's Gland Tumor", "Benign Bartholin Gland Neoplasm", "Bartholin gland benign neoplasm", "Benign Tumor of Bartholin's Gland", "Bartholin's gland benign neoplasm", "Benign Bartholin's Gland Neoplasm", "benign tumor of Bartholin's gland", "Benign neoplasm of Bartholin gland", "Benign Neoplasm of Bartholin's Gland", "benign neoplasm of Bartholin's gland", "Benign neoplasm of Bartholin's gland", "Benign Tumor of the Bartholin's Gland", "major vestibular gland benign neoplasm", "Benign Neoplasm of the Bartholin's Gland", "Benign neoplasm of Bartholin's gland (disorder)", "benign neoplasm of Bartholin's gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bartholin gland benign neoplasm", "shortest_name_length": 24}
{"curie": "MONDO:0014530", "names": ["SCAR18", "autosomal recessive spinocerebellar ataxia 18", "spinocerebellar ataxia, autosomal recessive 18", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18", "autosomal recessive spinocerebellar ataxia type 18", "spinocerebellar ataxia, autosomal recessive type 18", "Autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency", "autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency", "GRID2 autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome", "GRID2 autosomal recessive cerebellar ataxia - pyramidal signs - nystagmus - oculomotor apraxia syndrome", "Autosomal recessive congenital cerebellar ataxia due to ionotropic glutamate receptor delta-2 subunit deficiency", "autosomal recessive congenital cerebellar ataxia due to ionotropic glutamate receptor delta-2 subunit deficiency", "autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome caused by mutation in GRID2", "autosomal recessive cerebellar ataxia - pyramidal signs - nystagmus - oculomotor apraxia syndrome caused by mutation in GRID2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive spinocerebellar ataxia 18", "shortest_name_length": 6}
{"curie": "UMLS:C5447498", "names": ["Psammocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Psammocarcinoma", "shortest_name_length": 15}
{"curie": "MONDO:0100030", "names": ["adolescent/adult-onset epilepsy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adolescent/adult-onset epilepsy syndrome", "shortest_name_length": 40}
{"curie": "UMLS:C0333099", "names": ["fusiform aneurysm", "Fusiform aneurysm", "Fusiform Aneurysm", "Aneurysm, fusiform", "Aneurysm, Fusiform", "Fusiform Aneurysms", "Aneurysms, Fusiform", "Fusiform aneurysm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fusiform Aneurysm", "shortest_name_length": 17}
{"curie": "UMLS:C5419760", "names": ["Unresectable Nasopharyngeal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Nasopharyngeal Squamous Cell Carcinoma", "shortest_name_length": 51}
{"curie": "MONDO:0017615", "names": ["BFIS", "BFIE", "BFIC", "benign familial infantile seizures", "benign familial infantile epilepsy", "seizures, benign familial infantile", "benign familial infantile convulsion", "benign familial infantile convulsions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign familial infantile epilepsy", "shortest_name_length": 4}
{"curie": "MONDO:0010442", "names": ["SRXX3", "46,XX SEX reversal 3", "46,XX sex reversal 3", "46,XX SEX REVERSAL 3", "46,XX Sex reversal type 3", "46,XX SEX REVERSAL, SOX3-RELATED", "46,XX Sex reversal, Sox3-related", "CHROMOSOME Xq26 DELETION SYNDROME", "chromosome Xq26 deletion syndrome", "CHROMOSOME Xq26 DUPLICATION SYNDROME", "chromosome Xq26 Duplication syndrome", "46XX sex reversal 3, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XX sex reversal 3", "shortest_name_length": 5}
{"curie": "MONDO:0025351", "names": ["MCAND", "Linked syndrome", "LINKED SYNDROME", "MULTIPLE CONGENITAL ANOMALIES-NEURODEVELOPMENTAL SYNDROME, X-LINKED", "multiple congenital anomalies-neurodevelopmental syndrome, X-linked", "multiple congenital anomalies-neurodevelopmental syndrome, X-linked, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple congenital anomalies-neurodevelopmental syndrome, X-linked", "shortest_name_length": 5}
{"curie": "UMLS:C4288709", "names": ["Multinodular Adrenal Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Multinodular Adrenal Hyperplasia", "shortest_name_length": 32}
{"curie": "MONDO:0024882", "names": ["Metastasis", "Metastases", "Secondaries", "Secondary tumor", "secondary tumor", "Secondary Tumor", "Secondary cancer", "Tumor metastasis", "Tumor, secondary", "Secondary tumour", "Tumour metastasis", "CANCER METASTATIC", "Metastatic cancer", "Metastatic Cancer", "Secondary neoplasm", "Metastatic disease", "Secondary Neoplasm", "secondary neoplasm", "cancer; metastatic", "Metastatic neoplasm", "Neoplasm, secondary", "CA - Secondary cancer", "Secondary malignancies", "Secondary malignant deposit", "Metastatic malignant disease", "Metastatic neoplasm (disease)", "Metastatic malignant neoplasm", "Metastatic Malignant Neoplasm", "metastatic; cancer or neoplasm", "Secondary malignant neoplastic disease", "Metastatic malignant neoplasm (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary neoplasm", "shortest_name_length": 10}
{"curie": "MONDO:0010840", "names": ["Kuzniecky syndrome", "pachygyria, mental retardation and epilepsy", "Pachygyria, mental retardation and epilepsy", "pachygyria with mental retardation and seizures", "PACHYGYRIA WITH MENTAL RETARDATION AND SEIZURES", "Pachygyria with mental retardation and seizures", "pachygyria, intellectual disability and epilepsy", "pachygyria-intellectual disability-epilepsy syndrome", "Pachygyria-intellectual disability-epilepsy syndrome", "pachygyria with intellectual disability and seizures", "pachygyria, intellectual disability, epilepsy syndrome", "Pachygyria, intellectual disability, epilepsy syndrome", "Pachygyria, intellectual disability, epilepsy syndrome (disorder)", "pachygyria with mental retardation, seizures, and arachnoid cysts", "PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS", "pachygyria, intellectual disability, epilepsy syndrome (diagnosis)", "pachygyria with intellectual disability, seizures, and arachnoid cysts", "PACHYGYRIA WITH IMPAIRED INTELLECTUAL DEVELOPMENT, SEIZURES, AND ARACHNOID CYSTS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pachygyria-intellectual disability-epilepsy syndrome", "shortest_name_length": 18}
{"curie": "UMLS:C4744560", "names": ["Metastatic Lip Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Lip Squamous Cell Carcinoma", "shortest_name_length": 38}
{"curie": "UMLS:C4688276", "names": ["Recurrent EBV-Related Lymphoma", "Recurrent EBV-Associated Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent EBV-Related Lymphoma", "shortest_name_length": 30}
{"curie": "MONDO:0008084", "names": ["Neuropathy, congenital, with arthrogryposis multiplex", "neuropathy, congenital, with arthrogryposis multiplex", "NEUROPATHY, CONGENITAL, WITH ARTHROGRYPOSIS MULTIPLEX", "Congenital non-progressive peripheral neuropathy with arthrogryposis multiplex", "congenital non-progressive peripheral neuropathy with arthrogryposis multiplex"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuropathy, congenital, with arthrogryposis multiplex", "shortest_name_length": 53}
{"curie": "UMLS:C1333085", "names": ["Colon Carcinoma Metastatic in the Liver", "Colon Carcinoma Metastatic to the Liver"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colon Carcinoma Metastatic in the Liver", "shortest_name_length": 39}
{"curie": "MONDO:0000954", "names": ["Meckel diverticulum cancer", "Meckel's diverticulum cancer", "cancer of Meckel's diverticulum", "Malignant tumor of Meckel diverticulum", "Malignant tumour of Meckel diverticulum", "Malignant tumor of Meckel's diverticulum", "malignant Meckel's diverticulum neoplasm", "Malignant tumour of Meckel's diverticulum", "Malignant neoplasm of Meckel's diverticulum", "malignant neoplasm of Meckel's diverticulum", "Malignant neoplasm of meckel's diverticulum", "Malignant neoplasm of Meckel's diverticulum NOS", "Malignant tumor of Meckel's diverticulum (disorder)", "malignant small intestine neoplasm of Meckel's diverticulum", "malignant small intestine neoplasm of Meckel's diverticulum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meckel diverticulum cancer", "shortest_name_length": 26}
{"curie": "MONDO:0013922", "names": ["SCKL7", "Seckel syndrome 7", "SECKEL SYNDROME 7", "NIN Seckel syndrome", "Seckel syndrome type 7", "Seckel syndrome caused by mutation in NIN", "microcephalic primordial dwarfism, Dauber type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Seckel syndrome 7", "shortest_name_length": 5}
{"curie": "MONDO:0022349", "names": ["Absent septum pellucidum", "Missing septum pellucidum", "Septum pellucidum agenesis", "Absence of septum pellucidum", "absence of septum pellucidum", "Absence of the septum pellucidum", "Agenesis of the septum pellucidum", "congenital absence of septum pellucidum", "Absence of septum pellucidum (disorder)", "absence of septum pellucidum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital absence of septum pellucidum", "shortest_name_length": 24}
{"curie": "UMLS:C5557169", "names": ["Stage IIA1 Cervical Cancer AJCC v9", "Stage IIA1 Cervical Carcinoma AJCC v9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA1 Cervical Cancer AJCC v9", "shortest_name_length": 34}
{"curie": "MONDO:0004176", "names": ["Pediatric Extraosseous Osteosarcoma", "childhood extraosseous osteosarcoma", "Childhood Extraosseous Osteosarcoma", "pediatric extraosseous osteosarcoma", "Pediatric Extraskeletal Osteosarcoma", "Childhood Extraskeletal Osteosarcoma", "pediatric extraskeletal osteosarcoma", "pediatric extraskeletal Osteosarcoma", "childhood extraskeletal osteosarcoma", "extraosseous osteosarcoma of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood extraosseous osteosarcoma", "shortest_name_length": 35}
{"curie": "MONDO:0030859", "names": ["COACH2", "COACH syndrome 2", "COACH SYNDROME 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "COACH syndrome 2", "shortest_name_length": 6}
{"curie": "MONDO:0003284", "names": ["mediastinum leiomyoma", "mediastinal leiomyoma", "Mediastinal Leiomyoma", "Leiomyoma of Mediastinum", "leiomyoma of mediastinum", "Leiomyoma of the Mediastinum", "leiomyoma of the mediastinum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mediastinum leiomyoma", "shortest_name_length": 21}
{"curie": "MONDO:0018344", "names": ["periodic paralysis with transient compartment-like syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "periodic paralysis with transient compartment-like syndrome", "shortest_name_length": 59}
{"curie": "UMLS:C2986701", "names": ["Stage III Ovarian Low Malignant Potential Tumor", "stage III ovarian low malignant potential tumor", "stage III ovarian tumors of low malignant potential", "ovarian tumors of low malignant potential, stage III", "stage III borderline ovarian surface epithelial-stromal tumor", "Stage III Borderline Ovarian Surface Epithelial-Stromal Tumor", "borderline ovarian surface epithelial-stromal tumor, stage III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Borderline Ovarian Surface Epithelial-Stromal Tumor", "shortest_name_length": 47}
{"curie": "UMLS:C1263960", "names": ["coma diabetes", "Diabetic Coma", "Diabetic coma", "Coma;diabetic", "COMA DIABETIC", "diabetes coma", "diabetic coma", "Coma diabetic", "coma diabetic", "DIABETIC COMA", "Coma, Diabetic", "Diabetic Comas", "diabetic comas", "Comas, Diabetic", "Diabetic coma NOS", "Diabetic coma, NOS", "Diabetes with coma", "diabetes with coma", "hyperglycemic coma", "Coma hyperglycemic", "COMA HYPERGLYCEMIC", "Coma hyperglycaemic", "COMA HYPERGLYCAEMIC", "hyperglycemic; coma", "Coma due to diabetes mellitus", "Diabetes with coma (disorder)", "coma associated with diabetes mellitus", "Coma due to diabetes mellitus (disorder)", "coma associated with diabetes mellitus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diabetes with coma (disorder)", "shortest_name_length": 13}
{"curie": "MONDO:0017979", "names": ["ALPS", "FAS deficiency", "Canale-Smith syndrome", "Canale Smith Syndrome", "CANALE-SMITH SYNDROME", "Canale-Smith Syndrome", "Syndrome, Canale Smith", "Syndrome, Canale-Smith", "Canale-Smith Syndromes", "Syndromes, Canale-Smith", "AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME", "autoimmune lymphoproliferative syndrome", "Autoimmune Lymphoproliferative Syndrome", "Autoimmune lymphoproliferative syndrome", "Syndrome, Autoimmune Lymphoproliferative", "Autoimmune Lymphoproliferative Syndromes", "Lymphoproliferative Syndrome, Autoimmune", "Syndromes, Autoimmune Lymphoproliferative", "Lymphoproliferative Syndromes, Autoimmune", "Autoimmune Lymphoproliferative Syndrome (ALPS)", "Autoimmune lymphoproliferative syndrome [ALPS]", "ALPS (autoimmune lymphoproliferative syndrome)", "Autoimmune lymphoproliferative syndrome (disorder)", "autoimmune lymphoproliferative syndrome (diagnosis)", "autoimmune lymphoproliferative syndrome type 1, autosomal dominant", "AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE I, AUTOSOMAL DOMINANT", "Autoimmune Lymphoproliferative Syndrome, Type I, Autosomal Dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune lymphoproliferative syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0044872", "names": ["dysautonomia", "DYSAUTONOMIA", "Dysautonomia", "dysautonomias", "Dysautonomias", "Dysautonomia, NOS", "Primary Dysautonomia", "Autonomic dysfunction", "Primary Dysautonomias", "Dysautonomia, Primary", "Dysautonomias, Primary", "Autonomic dysregulation", "Abnormal autonomic nervous system physiology"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dysautonomia", "shortest_name_length": 12}
{"curie": "UMLS:C1336098", "names": ["Ureter Cancer Stage 0", "Stage 0 Ureter Cancer", "Stage 0 Ureter Carcinoma", "Stage 0 Ureteral Carcinoma", "Stage 0 Carcinoma of Ureter", "Stage 0 Ureter Cancer AJCC v7", "Stage 0 Carcinoma of the Ureter", "Stage 0 Ureter Urothelial Carcinoma", "Stage 0 Ureter Urothelial Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Ureter Cancer AJCC v7", "shortest_name_length": 21}
{"curie": "MONDO:0022559", "names": ["BACNS", "benign angiitis of the central nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign angiitis of the central nervous system", "shortest_name_length": 5}
{"curie": "UMLS:C0085090", "names": ["AIDS Lymphoma", "HIV related lymphoma", "HIV-Related Lymphoma", "HIV Related Lymphoma", "AIDS Related Lymphoma", "Lymphoma AIDS Related", "AIDS-related lymphoma", "Lymphoma AIDS related", "AIDS-Related Lymphoma", "aids-related lymphoma", "Lymphoma, HIV Related", "HIV-Related Lymphomas", "AIDS related lymphoma", "Lymphoma, HIV-Related", "AIDS-Related Lymphomas", "AIDS lymphomas related", "Lymphomas, HIV-Related", "lymphoma, AIDS-related", "aids-related lymphomas", "Lymphoma, AIDS Related", "Lymphoma, AIDS-related", "Lymphoma, AIDS-Related", "HIV Associated Lymphoma", "Lymphomas, AIDS-Related", "AIDS-Associated Lymphoma", "AIDS Associated Lymphoma", "AIDS-associated lymphoma", "AIDS-Associated Lymphomas", "Lymphoma, AIDS-Associated", "Lymphoma, AIDS Associated", "Lymphomas, AIDS-Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoma, AIDS-Related", "shortest_name_length": 13}
{"curie": "UMLS:C4761208", "names": ["Post 5-alpha-reductase inhibitor syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post 5-alpha-reductase inhibitor syndrome", "shortest_name_length": 41}
{"curie": "MONDO:0018541", "names": ["familial hypoaldosteronism", "Familial hypoaldosteronism", "Familial aldosterone deficiency", "Familial aldosterone deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial hypoaldosteronism", "shortest_name_length": 26}
{"curie": "MONDO:0006192", "names": ["EEC", "uterine endometrioid carcinoma", "endometrioid endomet. adenocar.", "Endometrioid endomet. adenocar.", "Endometrial Endometrioid Carcinoma", "Uterine Corpus Endometrioid Carcinoma", "uterine corpus endometrioid carcinoma", "Endometrioid Carcinoma of Endometrium", "Endometrioid carcinoma of endometrium", "endometrioid carcinoma of endometrium", "Endometrial Endometrioid Adenocarcinoma", "Endometrial endometrioid adenocarcinoma", "Endometrioid endometrial adenocarcinoma", "endometrial endometrioid adenocarcinoma", "endometrioid endometrial adenocarcinoma", "Endometrioid Carcinoma of the Endometrium", "endometrioid carcinoma of the endometrium", "Uterine Corpus Endometrioid Adenocarcinoma", "endometrioid adenocarcinoma of endometrium", "uterine corpus endometrioid adenocarcinoma", "Endometrioid Adenocarcinoma of Endometrium", "Endometrioid Adenocarcinoma of the Endometrium", "endometrioid adenocarcinoma of the endometrium", "Endometrioid carcinoma of endometrium (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometrial endometrioid adenocarcinoma", "shortest_name_length": 3}
{"curie": "MONDO:0001279", "names": ["Spinal Meningioma", "intraspinal meningioma", "Intraspinal Meningioma", "spinal canal and spinal cord meningioma", "Spinal Canal and Spinal Cord Meningioma", "Meningioma of Spinal Canal and Spinal Cord", "meningioma of spinal canal and spinal cord", "meningioma of the spinal canal and spinal cord", "Meningioma of the Spinal Canal and Spinal Cord"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intraspinal meningioma", "shortest_name_length": 17}
{"curie": "UMLS:C0280363", "names": ["Recurrent Lip and Oral Cavity Squamous Cell Cancer", "Recurrent Lip and Oral Cavity Squamous Cell Carcinoma", "lip and oral cavity squamous cell carcinoma, recurrent", "oral cavity and lip squamous cell carcinoma, recurrent", "epidermoid carcinoma of the lip and oral cavity, recurrent", "recurrent squamous cell carcinoma of the lip and oral cavity", "squamous cell carcinoma of the lip and oral cavity, recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Lip and Oral Cavity Squamous Cell Carcinoma", "shortest_name_length": 50}
{"curie": "MONDO:0013058", "names": ["CLWM", "RNAse T2-deficient leukoencephalopathy", "RNASET2-deficient cystic leukoencephalopathy", "cystic leukoencephalopathy without megalencephaly", "Cystic leukoencephalopathy without megalencephaly", "Cystic leucoencephalopathy without megalencephaly", "Leukoencephalopathy, Cystic, Without Megalencephaly", "leukoencephalopathy, cystic, without megalencephaly", "LEUKOENCEPHALOPATHY, CYSTIC, WITHOUT MEGALENCEPHALY", "infantile-onset RNASET2 deficient cystic leukoencephalopathy", "Cystic leukoencephalopathy without megalencephaly (disorder)", "Cystic leukoencephalopathy without megalencephaly (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cystic leukoencephalopathy without megalencephaly", "shortest_name_length": 4}
{"curie": "MONDO:0012126", "names": ["ANFH", "ANFH1", "Femur Head Necrosis", "femur head necrosis", "FEMUR HEAD NECROSIS", "Femur Head Necroses", "Head Necrosis, Femur", "Necrosis, Femur Head", "osteonecrosis of femoral head", "FEMORAL HEAD NECROSIS ASEPTIC", "Aseptic Necrosis of Femur Head", "Aseptic necrosis of femoral head", "aseptic necrosis of femoral head", "Necrosis, Aseptic, of Femur Head", "Aseptic Necrosis of Femoral Head", "aseptic Necrosis of femoral head", "femoral head, aseptic Necrosis of", "aseptic Necrosis of head of femur", "ischemic Necrosis of femoral head", "Aseptic necrosis of head of femur", "Aseptic Necrosis of Head of Femur", "femoral head, avascular Necrosis of", "Familial osteonecrosis of the femoral head", "familial osteonecrosis of the femoral head", "familial avascular necrosis of femoral head", "Familial avascular necrosis of femoral head", "avascular NECROSIS of femoral head, primary", "Aseptic necrosis of head of femur (disorder)", "Familial avascular necrosis of head of femur", "aseptic necrosis of femoral head due to drugs", "avascular NECROSIS of femoral head, primary, 1", "primary avascular necrosis of the femoral head", "avascular Necrosis of femoral head, primary, 1", "familial avascular necrosis of the femoral head", "Familial avascular necrosis of head of femur (disorder)", "aseptic necrosis of femoral head due to drugs (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial avascular necrosis of femoral head", "shortest_name_length": 4}
{"curie": "UMLS:C0269800", "names": ["water leak", "Amniorrhea", "Amniorrhoea", "leaking water", "Waters leaking", "Liquor draining", "Liquor observed", "Drainage of liquor", "amniotic fluid leak", "Amniotic Fluid Leak", "amniotic fluid leaks", "amniotic fluid; leak", "amniotic fluid leakage", "amniotic fluid leaking", "leaking amniotic fluid", "Amniotic fluid leakage", "Amniotic fluid leaking", "Flow of amniotic liquor", "Leakage of amniotic fluid", "leakage of amniotic fluid", "Leakage of Amniotic Fluid", "Amniotic fluid leaking (disorder)", "amniotic fluid leaking (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Amniotic fluid leaking", "shortest_name_length": 10}
{"curie": "UMLS:C0948486", "names": ["Acquired esophageal web", "Acquired oesophageal web"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired esophageal web", "shortest_name_length": 23}
{"curie": "UMLS:C0008066", "names": ["behavior child disorder", "child behavior disorder", "Child Behavior Disorder", "Child Behavior Disorders", "child behavior disorders", "Behavior Disorder, Child", "Childhood Behavior Disorder", "Childhood Behavior Disorders", "Behavior Disorder, Childhood", "Disorder, Childhood Behavior", "Behavior disorders in children"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Child Behavior Disorders", "shortest_name_length": 23}
{"curie": "MONDO:0011139", "names": ["Preaxial foot polydactyly", "Preaxial polydactyly, feet", "Preaxial polydactyly of foot", "Preaxial polydactyly of feet", "preaxial polydactyly of feet", "preaxial hallucal polydactyly", "PREAXIAL HALLUCAL POLYDACTYLY", "Preaxial Hallucal Polydactyly", "Preaxial hallucal polydactyly", "Preaxial polydactyly of the feet", "Polydactyly affecting the hallux", "preaxial polydactyly of feet (physical finding)", "Partial/complete duplication of the phalanges of the big toe"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "preaxial hallucal polydactyly", "shortest_name_length": 25}
{"curie": "UMLS:C0037580", "names": ["soft swelling tissue", "soft tissue swelling", "SOFT TISSUE SWELLING", "Soft tissue swelling", "soft tissue swelling (symptom)", "Soft tissue swelling (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Soft tissue swelling", "shortest_name_length": 20}
{"curie": "MONDO:0015436", "names": ["R20", "Ring 20", "R(20) Syndrome", "r(20) syndrome", "Ring 20 Syndrome", "chromosome 20 ring", "Ring chromosome 20", "ring chromosome 20", "Ring Chromosome 20", "chromosome ring 20", "Ring chromosome type 20", "Ring chromosome 20 syndrome", "Ring Chromosome 20 Syndrome", "chromosome 20 ring syndrome", "Ring Chromosome 20 Epilepsy Syndrome", "Ring chromosome 20 syndrome (disorder)", "Ring chromosome 20 syndrome (diagnosis)", "anomaly of chromosome pair ring 20 syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ring chromosome 20", "shortest_name_length": 3}
{"curie": "UMLS:C4521875", "names": ["Stage II Pancreatic Cancer", "Stage II Pancreatic Cancer AJCC v8", "Stage II Exocrine Pancreatic Cancer AJCC v8", "Stage II Exocrine Pancreatic Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Pancreatic Cancer AJCC v8", "shortest_name_length": 26}
{"curie": "UMLS:C1336817", "names": ["Transplant-Related Bladder Urothelial Carcinoma", "Transplant-Related Bladder Transitional Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transplant-Related Bladder Urothelial Carcinoma", "shortest_name_length": 47}
{"curie": "UMLS:C5670652", "names": ["ELP1-Associated Medulloblastoma", "ELP1-Associated Medulloblastoma, SHH-Activated, TP53-Wildtype"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ELP1-Associated Medulloblastoma", "shortest_name_length": 31}
{"curie": "UMLS:C1514512", "names": ["Prostate Ductal Adenocarcinoma, Papillary Pattern"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Ductal Adenocarcinoma, Papillary Pattern", "shortest_name_length": 49}
{"curie": "UMLS:C1336338", "names": ["Stage IVA Extrahepatic Bile Duct Cancer", "Extrahepatic Bile Duct Cancer Stage IVA", "Stage IVA Extrahepatic Bile Duct Carcinoma", "Stage IVA Carcinoma of Extrahepatic Bile Duct", "Stage IVA Carcinoma of the Extrahepatic Bile Duct"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Extrahepatic Bile Duct Cancer", "shortest_name_length": 39}
{"curie": "MONDO:0060556", "names": ["JLSM", "JOINT LAXITY, SHORT STATURE, AND MYOPIA", "joint laxity, short stature, and myopia", "Severe myopia-generalized joint laxity-short stature syndrome", "Severe myopia, generalized joint laxity, short stature syndrome", "Severe myopia, generalised joint laxity, short stature syndrome", "Severe myopia, generalized joint laxity, short stature syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "joint laxity, short stature, and myopia", "shortest_name_length": 4}
{"curie": "UMLS:C5418957", "names": ["Metastatic Primary Peritoneal Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Primary Peritoneal Serous Adenocarcinoma", "shortest_name_length": 51}
{"curie": "MONDO:0016498", "names": ["acute pure sensory GBS", "acute pure sensory neuropathy", "acute pure sensory Guillain-Barré syndrome", "acute pure sensory Guillain-BarrC) syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute pure sensory neuropathy", "shortest_name_length": 22}
{"curie": "MONDO:0016905", "names": ["6q deletion", "Deletion 6q", "monosomy 6q", "deletion 6q", "Monosomy 6q", "6q monosomy", "6q- syndrome", "del(6q) syndrome", "partial monosomy 6q", "6q deletion syndrome", "deletion 6q syndrome", "chromosome 6q monosomy", "chromosome 6q deletion", "Chromosome 6, monosomy 6q", "chromosome 6q deletion syndrome", "Partial monosomy of chromosome 6q", "Partial deletion of chromosome 6q", "partial monosomy of chromosome 6q", "partial deletion of chromosome 6q", "Partial monosomy of the long arm of chromosome 6", "partial monosomy of the long arm of chromosome 6", "partial deletion of the long arm of chromosome 6", "Partial deletion of the long arm of chromosome 6", "partial deletion of the long arm of chromosome type 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of the long arm of chromosome 6", "shortest_name_length": 11}
{"curie": "MONDO:0020584", "names": ["anemia; enzyme disorder", "enzyme disorder; anemia", "Anemia due to enzymopathy", "Anaemia due to enzymopathy", "Anemia due to enzyme disorder", "anemia due to enzyme disorder", "Anemia due to Enzyme Disorder", "anemia due to enzyme disorders", "Anemia due to enzyme disorders", "Anaemia due to enzyme disorder", "Anaemia due to enzyme disorders", "Anemia due to enzymopathy (disorder)", "hemolytic; anemia, due to enzyme disorder", "anemia; hemolytic, due to enzyme disorder", "anemia due to enzyme disorders (diagnosis)", "Anemia due to enzyme disorder, unspecified", "Anaemia due to enzyme disorder, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anemia due to enzyme disorder", "shortest_name_length": 23}
{"curie": "MONDO:0015323", "names": ["teratogenic Pierre Robin syndrome", "teratogenic Pierre Robin sequence"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "teratogenic Pierre Robin syndrome", "shortest_name_length": 33}
{"curie": "MONDO:0015628", "names": ["VWD2A", "Type 2A von Willebrand Disease", "Von Willebrand disease type 2A", "von Willebrand disease type 2A", "VON WILLEBRAND DISEASE, TYPE 2A", "Type IIA von Willebrand Disease", "von Willebrand disease, type 2A", "von Willebrand Disease, Type 2A", "Von Willebrand disease, type 2A", "von Willebrand disease, type IIA", "von Willebrand Disease, Type IIA", "Hereditary von Willebrand disease type 2A", "von Willebrand disease type 2A (diagnosis)", "Hereditary von Willebrand disease type 2A (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "von Willebrand disease type 2A", "shortest_name_length": 5}
{"curie": "UMLS:C0235649", "names": ["BREAST EDEMA", "Breast edema", "edema breast", "breast edema", "breasts edema", "Breast oedema", "BREAST OEDEMA", "Edema of breast", "Oedema of breast", "Edema of breast (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Edema of breast", "shortest_name_length": 12}
{"curie": "UMLS:C1403753", "names": ["penis; melanoma", "Penile Melanoma", "melanoma; penis", "melanoma of penis", "Melanoma of the Penis", "melanoma of penis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melanoma of penis", "shortest_name_length": 15}
{"curie": "UMLS:C0919691", "names": ["anastomotic leak", "Anastomotic leak", "Anastomotic Leak", "Leak, Anastomotic", "anastomotic leaks", "Anastomotic Leaks", "Leaks, Anastomotic", "Anastomotic Leakage", "Leakage, Anastomotic", "Anastomotic Leakages", "Leakages, Anastomotic", "anastomotic leak (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anastomotic Leak", "shortest_name_length": 16}
{"curie": "MONDO:0006842", "names": ["Lymphangiomyoma", "lymphangiomyoma", "Lymphangiomyomas", "Lymphangioleiomyoma", "lymphangioleiomyoma", "Lymphangioleiomyomas", "Lymphangiomyoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphangiomyoma", "shortest_name_length": 15}
{"curie": "UMLS:C3854434", "names": ["Bone marrow infiltration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone marrow infiltration", "shortest_name_length": 24}
{"curie": "MONDO:0010013", "names": ["SHNKND", "SLC35D1-CDG", "Snail-like ilia", "Snail-shaped ilia", "Snail-like pelvis", "schneckenbecken dysplasia", "Schneckenbecken dysplasia", "SCHNECKENBECKEN DYSPLASIA", "Schneckenbecken dysplasia (disorder)", "chondrodysplasia with snail-like pelvis", "Chondrodysplasia with snail-like pelvis", "chondrodysplasia lethal neonatal with snail like pelvis", "Chondrodysplasia, lethal neonatal, with snail-like pelvis", "chondrodysplasia, lethal neonatal, with snail-like pelvis", "CHONDRODYSPLASIA, LETHAL NEONATAL, WITH SNAIL-LIKE PELVIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schneckenbecken dysplasia", "shortest_name_length": 6}
{"curie": "MONDO:0008306", "names": ["FBD", "Bri amyloidosis", "ABri amyloidosis", "Familial British Dementia", "familial British dementia", "dementia familial British", "dementia, familial British", "DEMENTIA, FAMILIAL BRITISH", "AMYLOIDOSIS, VAN ALLEN TYPE", "Familial dementia British type", "Familial dementia, British type", "familial dementia, British type", "Iowa type amyloid polyneuropathy", "British Type Amyloid Polyneuropathy", "British type amyloid polyneuropathy", "Amyloid Polyneuropathy, British Type", "[OBSOLETE] Dementia, familial British", "Van Allen type amyloid polyneuropathy", "PRESENILE DEMENTIA WITH SPASTIC ATAXIA", "Presenile Dementia with Spastic Ataxia", "presenile dementia with spastic ataxia", "Familial amyloid polyneuropathy type III", "Familial dementia British type (disorder)", "cerebral amyloid angiopathy, British type", "CEREBRAL AMYLOID ANGIOPATHY, BRITISH TYPE", "Cerebral Amyloid Angiopathy, British Type", "Familial dementia, British type (diagnosis)", "ITM2B-related cerebral amyloid angiopathy 1", "cerebral amyloid angiopathy, ITM2B-RELATED, 1", "CEREBRAL AMYLOID ANGIOPATHY, ITM2B-RELATED, 1", "Familial British dementia with amyloid angiopathy", "cerebral amyloid angiopathy, ITM2B-related, type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ABri amyloidosis", "shortest_name_length": 3}
{"curie": "MONDO:0020494", "names": ["OOD", "OCULOOTODENTAL SYNDROME", "Oculootodental syndrome", "oculootodental syndrome", "Oculootodental Syndrome", "Otodental Syndrome With Coloboma", "OTODENTAL SYNDROME WITH COLOBOMA", "Oculootodental syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculootodental syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0016248", "names": ["familial ovarian cancer", "hereditary ovarian cancer", "familial ovarian malignant tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial ovarian cancer", "shortest_name_length": 23}
{"curie": "UMLS:C4521732", "names": ["Stage III Esophageal Squamous Cell Cancer", "Postneoadjuvant Therapy Stage III Esophageal Squamous Cell Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postneoadjuvant Therapy Stage III Esophageal Squamous Cell Carcinoma AJCC v8", "shortest_name_length": 41}
{"curie": "MONDO:0014587", "names": ["CMS9", "congenital myasthenic syndrome 9", "MUSK congenital myasthenic syndrome", "congenital myasthenic syndrome type 9", "congenital myasthenic syndrome caused by mutation in MUSK", "congenital myasthenic syndrome 9, associated with acetylcholine receptor deficiency", "myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency", "MYASTHENIC SYNDROME, CONGENITAL, 9, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myasthenic syndrome 9", "shortest_name_length": 4}
{"curie": "MONDO:0021528", "names": ["benign Male breast tumor", "Neoplasm benign;breast;M", "Benign Male Breast Tumor", "benign male breast neoplasm", "Breast neoplasm benign male", "benign tumor of Male breast", "benign tumor of male breast", "Benign Male Breast Neoplasm", "Benign Tumor of Male Breast", "male breast benign neoplasm", "benign Male breast neoplasm", "Benign neoplasm of male breast", "Benign Neoplasm of Male Breast", "benign neoplasm of male breast", "benign tumor of the Male breast", "Benign Tumor of the Male Breast", "benign neoplasm of the male breast", "Benign Neoplasm of the Male Breast", "benign neoplasm of the Male breast", "Benign neoplasm of male breast, NOS", "Benign neoplasm of male breast (disorder)", "benign neoplasm of male breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of male breast", "shortest_name_length": 24}
{"curie": "UMLS:C1711171", "names": ["Conventional Heart Rhabdomyoma", "Conventional Cardiac Rhabdomyoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conventional Cardiac Rhabdomyoma", "shortest_name_length": 30}
{"curie": "MONDO:0019032", "names": ["MRGH", "MENTAL RETARDATION, X-LINKED, WITH ISOLATED GROWTH HORMONE DEFICIENCY", "Mental Retardation, X-Linked, with Isolated Growth Hormone Deficiency", "X-linked intellectual disability with isolated growth hormone deficiency", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, WITH ISOLATED GROWTH HORMONE DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability with isolated growth hormone deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0023540", "names": ["Kashani-Strom-Utley syndrome", "Kashani Strom Utley syndrome", "Pulmonary aortic stenosis obstructive uropathy", "pulmonary aortic stenosis obstructive uropathy", "hypoplastic pulmonary arteries and aorta with obstructive uropathy", "Hypoplastic pulmonary arteries and aorta with obstructive uropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kashani-Strom-Utley syndrome", "shortest_name_length": 28}
{"curie": "UMLS:C0266090", "names": ["cheilognathouranoschisis", "Cheilognathouranoschisis", "cheilognathopalatoschisis", "CHEILOGNATHOPALATOSCHISIS", "Cheilognathopalatoschisis", "Cheilognathouranoschisis (disorder)", "Cheilognathouranoschisis (diagnosis)", "Cleft upper lip, upper jaw and palate", "Cleft upper lip, upper jaw AND palate", "Cheilognathopalatoschisis (diagnosis)", "cleft upper lip, upper jaw and palate", "Cleft upper lip, upper jaw, and palate", "Cleft upper lip, upper jaw AND palate (disorder)", "cleft upper lip, upper jaw and palate (diagnosis)", "cleft palate with cleft lip cheilognathouranoschisis", "cleft palate with cleft lip cheilognathopalatoschisis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cheilognathouranoschisis", "shortest_name_length": 24}
{"curie": "MONDO:0004859", "names": ["Hydrocholecystis", "Gallbladder edema", "Gallbladder oedema", "Gallbladder Hydrops", "gallbladder hydrops", "hydrops gallbladder", "gallbladder; hydrops", "GALLBLADDER, HYDROPS", "hydrops; gallbladder", "Hydrops, gallbladder", "Edematous gallbladder", "Hydrops of gallbladder", "hydrops of gallbladder", "Edematous gallbladder (finding)", "Hydrops of gallbladder (disorder)", "hydrops of gallbladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hydrops of gallbladder", "shortest_name_length": 16}
{"curie": "MONDO:0001542", "names": ["common peroneal nerve lesion", "Common peroneal nerve lesion", "Lateral popliteal nerve lesion", "Lesion of common peroneal nerve", "Lesion of lateral popliteal nerve", "Lateral popliteal nerve lesion NOS", "Lesion of common peroneal nerve, NOS", "Lesion of lateral popliteal nerve, NOS", "Common peroneal nerve lesion (disorder)", "common peroneal nerve lesion (diagnosis)", "common fibular nerve peripheral nerve lesion", "peripheral nerve lesion of common fibular nerve", "Lesion of lateral popliteal nerve, unspecified lower limb"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "common peroneal nerve lesion", "shortest_name_length": 28}
{"curie": "MONDO:0016448", "names": ["PXE-PDE", "PXE-like papillary dermal elastolysis", "Pseudoxanthoma elasticum-like papillary dermal elastolysis", "pseudoxanthoma elasticum-like papillary dermal elastolysis", "Pseudoxanthoma elasticum-like papillary dermal elastolysis (disorder)", "PXE-like (pseudoxanthoma elasticum-like) papillary dermal elastolysis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudoxanthoma elasticum-like papillary dermal elastolysis", "shortest_name_length": 7}
{"curie": "MONDO:0016355", "names": ["semilobar holoprosencephaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "semilobar holoprosencephaly", "shortest_name_length": 27}
{"curie": "UMLS:C5446363", "names": ["Locally Advanced Triple-Negative Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Triple-Negative Breast Carcinoma", "shortest_name_length": 49}
{"curie": "MONDO:0003403", "names": ["Testicular nonseminomat. GCT, NOS", "Testicular Non-Seminomatous Germ Cell Cancer", "testicular non-seminomatous germ cell cancer", "Testicular nonseminomatous germ cell tumor, NOS", "malignant non-seminomatous germ cell tumor of testis", "malignant Non-Seminomatous germ cell tumor of testis", "Malignant Non-Seminomatous Germ Cell Tumor of Testis", "Malignant Non-Seminomatous Germ Cell Cancer of Testis", "malignant non-seminomatous germ cell cancer of testis", "malignant testicular non-seminomatous germ cell tumor", "Malignant Testicular Non-Seminomatous Germ Cell Tumor", "testicular germ cell tumor non-seminomatous, malignant", "testicular non-seminomatous germ cell tumor, malignant", "Malignant Non-Seminomatous Germ Cell Neoplasm of Testis", "malignant non-seminomatous germ cell neoplasm of testis", "Malignant Non-Seminomatous Germ Cell Tumor of the Testis", "testicular non-seminomatous malignant germ cell neoplasm", "Testicular Non-Seminomatous Malignant Germ Cell Neoplasm", "malignant non-seminomatous germ cell tumor of the testis", "malignant testicular non-seminomatous germ cell neoplasm", "Malignant Testicular Non-Seminomatous Germ Cell Neoplasm", "malignant non-seminomatous germ cell cancer of the testis", "Malignant Non-Seminomatous Germ Cell Cancer of the Testis", "malignant non-seminomatous germ cell neoplasm of the testis", "Malignant Non-Seminomatous Germ Cell Neoplasm of the Testis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular non-seminomatous germ cell cancer", "shortest_name_length": 33}
{"curie": "MONDO:0014638", "names": ["FANCT", "UBE2T Fanconi anemia", "Fanconi anemia complementation group T", "FANCONI ANEMIA, COMPLEMENTATION GROUP T", "Fanconi anemia, complementation group T", "Fanconi anemia caused by mutation in UBE2T", "Fanconi anemia complementation group type T", "Fanconi Anemia, complementation group type T"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fanconi anemia complementation group T", "shortest_name_length": 5}
{"curie": "UMLS:C4054392", "names": ["Nephrotic Syndrome - CRB2 Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - CRB2 Associated", "shortest_name_length": 36}
{"curie": "MONDO:0012659", "names": ["ARMD9", "age related macular degeneration 9", "C3 age-related macular degeneration", "Macular Degeneration, Age-Related, 9", "macular degeneration, age-related, 9", "MACULAR DEGENERATION, AGE-RELATED, 9", "age related macular degeneration type 9", "macular Degeneration, age-related, type 9", "age-related macular degeneration caused by mutation in C3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "age related macular degeneration 9", "shortest_name_length": 5}
{"curie": "MONDO:0009264", "names": ["eventration", "Eventration", "Laparoschisis", "gastroschisis", "Gastroschises", "GASTROSCHISIS", "Gastroschisis", "laparoschisis", "gastroschises", "abdominal wall defects", "Gastroschisis (disorder)", "gastroschisis (diagnosis)", "congenital fissure of the abdominal cavity", "Congenital Fissure of the Abdominal Cavity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastroschisis", "shortest_name_length": 11}
{"curie": "OMIM:267800", "names": ["Retinal Dystrophy, Reticular Pigmentary, of Posterior Pole", "RETINAL DYSTROPHY, RETICULAR PIGMENTARY, OF POSTERIOR POLE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 58}
{"curie": "UMLS:C4086185", "names": ["Cleft Maxilla"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cleft Maxilla", "shortest_name_length": 13}
{"curie": "UMLS:C3146269", "names": ["VAIN 3", "VAIN III", "VAIN 3 AJCC v7", "VAIN III AJCC v7", "Stage 0 Vaginal Cancer", "Stage 0 Vaginal Cancer AJCC v7", "stage 0 vaginal carcinoma in situ", "Vaginal Intraepithelial Neoplasia Grade 3", "Grade III Vaginal Intraepithelial Neoplasia", "Vaginal Intraepithelial Neoplasia Grade 3 AJCC v7", "Grade III Vaginal Intraepithelial Neoplasia AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Vaginal Cancer AJCC v7", "shortest_name_length": 6}
{"curie": "MONDO:0019076", "names": ["circumscribed palmoplantar hypokeratosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "circumscribed palmoplantar hypokeratosis", "shortest_name_length": 40}
{"curie": "MONDO:0032866", "names": ["CDCBM10", "cortical dysplasia, complex, with other brain malformations 10", "CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cortical dysplasia, complex, with other brain malformations 10", "shortest_name_length": 7}
{"curie": "UMLS:C5206572", "names": ["Thymic Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thymic Neuroendocrine Neoplasm", "shortest_name_length": 30}
{"curie": "UMLS:C5420863", "names": ["Recurrent Thyroid Gland Oncocytic Carcinoma", "Recurrent Thyroid Gland Hurthle Cell Carcinoma", "Recurrent Thyroid Gland Oncocytic (Hurthle Cell) Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Thyroid Gland Oncocytic Carcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0006157", "names": ["colorectal adenosquamous cancer", "colorectum adenosquamous carcinoma", "colorectal adenosquamous carcinoma", "Colorectal Adenosquamous Carcinoma", "Colorectal (Colon or Rectal) Adenosquamous Cancer", "colorectal (colon or rectal) adenosquamous cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorectal adenosquamous carcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C0276090", "names": ["Coliform arthritis", "Arthritis due to E. coli", "Arthritis caused by E. coli", "Arthritis due to Escherichia coli", "Coliform arthritis or polyarthritis", "Arthritis caused by Escherichia coli", "Arthritis or polyarthritis due to coliform", "Escherichia coli arthritis or polyarthritis", "Arthritis caused by Escherichia coli (disorder)", "Arthritis or polyarthritis due to Escherichia coli", "Arthritis or Polyarthritis due to Escherichia Coli"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arthritis due to E. coli", "shortest_name_length": 18}
{"curie": "MONDO:0007426", "names": ["deafness ear one", "deafness one ear", "Deafness;one ear", "Deafness in one ear", "DEAFNESS UNILATERAL", "Deafness unilateral", "unilateral deafness", "Deafness Unilateral", "Unilateral deafness", "Unilateral Deafness", "deafness, unilateral", "Deafness, Unilateral", "DEAFNESS, UNILATERAL", "Deafness, unilateral", "Unilateral, Deafness", "Hypoacusis unilateral", "Unilateral Hearing Loss", "HEARING LOSS UNILATERAL", "hearing loss unilateral", "unilateral hearing loss", "Unilateral hearing loss", "Hearing loss unilateral", "Hearing Loss, Unilateral", "Hearing loss, unilateral", "[OBSOLETE] Deafness, Unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness, unilateral", "shortest_name_length": 16}
{"curie": "MONDO:0008903", "names": ["lung cancer", "Lung cancer", "LUNG CANCER", "Lung Cancer", "lung cancers", "lungs cancer", "Cancer, Lung", "Lung Cancers", "Lungs--Cancer", "Cancers, Lung", "cancers lungs", "lung neoplasm", "cancer of lung", "Cancer of lung", "Cancer of Lung", "lung malignancy", "Lung cancer NOS", "LUNG MALIGNANCY", "cancer pulmonary", "CA - Lung cancer", "Pulmonary Cancer", "pulmonary cancer", "lung malignancies", "Cancer, Pulmonary", "Pulmonary Cancers", "cancer of the lung", "Cancers, Pulmonary", "Cancer of the Lung", "Neoplasm malig;lung", "Malignant Lung Tumor", "lung cancer, somatic", "malignant lung tumor", "LUNG CANCER MALIGNANT", "lung malignant tumors", "Malignant lung tumors", "lung malignant tumours", "malignant lung neoplasm", "alveolar cell carcinoma", "malignant tumor of lung", "Lung neoplasm malignant", "Malignant tumor of lung", "MALIGNANT LUNG NEOPLASM", "Malignant Tumor of Lung", "Malignant Lung Neoplasm", "lung cancer (diagnosis)", "malignant neoplasm lung", "Malignant tumour of lung", "Nonsmall cell lung cancer", "malignant neoplasm of lung", "Malignant neoplasm of lung", "Malignant Neoplasm of Lung", "malignant tumor of the lung", "Malignant Tumor of the Lung", "malignant neoplasm of the lung", "Malignant Neoplasm of the Lung", "LUNG CANCER, PROTECTION AGAINST", "malignant neosplasm of the lung", "Malignant neoplasm of lung, NOS", "lung cancer, protection against", "adenocarcinoma of lung, somatic", "Malignant tumor of lung (disorder)", "nonsmall cell lung cancer, somatic", "malignant neoplasm of lung (diagnosis)", "Malignant neoplasm of lower lobe, bronchus or lung", "Malignant neoplasm of upper lobe, bronchus or lung", "malignant neoplasm of upper lobe, bronchus, or lung", "Malignant neoplasm of middle lobe, bronchus or lung", "malignant neoplasm of lower lobe, bronchus, or lung", "malignant neoplasm of middle lobe, bronchus, or lung", "Malignant neoplasm of other parts of bronchus or lung", "lung neoplasm malignant of lower lobe, bronchus, or lung", "lung neoplasm malignant of upper lobe, bronchus, or lung", "lung neoplasm malignant of middle lobe, bronchus, or lung", "Malignant neoplasm of upper lobe, bronchus or lung (disorder)", "malignant neoplasm of lower lobe, bronchus, or lung (diagnosis)", "malignant neoplasm of upper lobe, bronchus, or lung (diagnosis)", "lung cancer, resistance to, autosomal dominant, somatic mutation", "malignant neoplasm of middle lobe, bronchus, or lung (diagnosis)", "lung cancer, susceptibility to, autosomal dominant, somatic mutation", "lung cancer, protection against, autosomal dominant, somatic mutation", "nonsmall cell lung cancer, susceptibility to, autosomal dominant, somatic mutation", "adenocarcinoma of lung, response to tyrosine kinase inhibitor in, autosomal dominant, somatic mutation", "nonsmall cell lung cancer, response to tyrosine kinase inhibitor in, autosomal dominant, somatic mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung cancer", "shortest_name_length": 11}
{"curie": "MONDO:0025505", "names": ["mink viral enteritis", "Mink Viral Enteritis", "Viral Enteritis, Mink", "viral enteritis, mink", "Enteritis, Mink Viral", "enteritis, mink viral", "mink viral enteritides", "Mink Viral Enteritides", "Enteritides, Mink Viral", "viral enteritides, mink", "Viral Enteritides, Mink", "enteritides, mink viral", "enteritis, infectious, of mink", "Enteritis, Infectious, of Mink"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mink viral enteritis", "shortest_name_length": 20}
{"curie": "UMLS:C0857501", "names": ["Acute schizophrenia", "Acute Schizophrenia", "acute schizophrenia", "acute; schizophrenic", "schizophrenia; acute"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute schizophrenia", "shortest_name_length": 19}
{"curie": "MONDO:0004625", "names": ["Phlebitis", "phlebitis", "PHLEBITIS", "Phlebitides", "phlebitides", "Phlebitis NOS", "Phlebitis, NOS", "PHLEBITIS ALONE", "Inflammation;vein", "vein inflammation", "inflammation, vein", "inflammation; vein", "vein; inflammation", "Phlebitis (disorder)", "inflammation of vein", "Inflammation of vein", "phlebitis (diagnosis)", "inflammation of the vein", "Inflammation of vein, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phlebitis", "shortest_name_length": 9}
{"curie": "MONDO:0019102", "names": ["Dentinogenesis imperfecta-short stature-deafness-intellectual disability syndrome", "Dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome", "dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome", "Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome", "Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome (disorder)", "Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome", "shortest_name_length": 81}
{"curie": "UMLS:C0086168", "names": ["Dissociation", "dissociation", "Dissociation - mental defense mechanism", "Dissociation - mental defence mechanism", "Dissociation - mental defense mechanism (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dissociation", "shortest_name_length": 12}
{"curie": "MONDO:0009435", "names": ["Goldblatt-Wallis syndrome", "Goldblatt Wallis syndrome", "hypospadias mental retardation syndrome", "Hypospadias-Mental Retardation Syndrome", "HYPOSPADIAS-MENTAL RETARDATION SYNDROME", "hypospadias-mental retardation syndrome", "hypospadias intellectual disability syndrome", "hypospadias-intellectual disability syndrome", "hypospadias mental retardation Goldblatt type", "hypospadias intellectual deficit Goldblatt type", "hypospadias intellectual disability Goldblatt type", "hypospadias-intellectual disability, Goldblatt type syndrome", "Hypospadias-intellectual disability, Goldblatt type syndrome", "Hypospadias and intellectual disability syndrome Goldblatt type", "Hypospadias and intellectual disability syndrome Goldblatt type (disorder)", "Hypospadias and intellectual disability syndrome Goldblatt type (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypospadias-intellectual disability, Goldblatt type syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0044014", "names": ["thyroiditis postpartum", "Postpartum Thyroiditis", "postpartum thyroiditis", "Postpartum thyroiditis", "postpartum; thyroiditis", "Post partum Thyroiditis", "Thyroiditis, Postpartum", "post partum thyroiditis", "post-partum thyroiditis", "thyroiditis; postpartum", "Post-partum Thyroiditis", "thyroiditis, postpartum", "Thyroiditis, Post-partum", "postpartum thyroiditides", "thyroiditis, post-partum", "Postpartum Thyroiditides", "post-partum thyroiditides", "Thyroiditides, Postpartum", "thyroiditides, postpartum", "Post-partum Thyroiditides", "Thyroiditides, Post-partum", "thyroiditides, post-partum", "Postpartum thyroiditis (disorder)", "postpartum thyroiditis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postpartum thyroiditis", "shortest_name_length": 22}
{"curie": "MONDO:0008893", "names": ["OTCS", "C SYNDROME", "syndrome c", "c syndrome", "C syndrome", "Opitz C trigonocephaly", "Trigonocephaly syndrome", "TRIGONOCEPHALY SYNDROME", "trigonocephaly syndrome", "Trigonocephaly C syndrome", "trigonocephaly C syndrome", "opitz trigonocephaly syndrome", "OPITZ TRIGONOCEPHALY SYNDROME", "Opitz trigonocephaly syndrome", "Opitz trigonocephaly C syndrome", "Trigonocephaly C syndrome (disorder)", "Trigonocephaly C syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "C syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0014697", "names": ["CVID12", "NFKB1 DEFICIENCY", "NFKB1 deficiency", "common variable immunodeficiency 12", "immunodeficiency, common variable, 12", "NFKB1 common variable immunodeficiency", "immunodeficiency, common variable, type 12", "IMMUNODEFICIENCY, COMMON VARIABLE, 12, WITH AUTOIMMUNITY", "common variable immunodeficiency caused by mutation in NFKB1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency, common variable, 12", "shortest_name_length": 6}
{"curie": "UMLS:C1519276", "names": ["Sex cord tumor with annular tubules", "Ovarian Sex Cord Tumor with Annular Tubules", "Ovarian Sex Cord Neoplasm with Annular Tubules", "Ovarian Sertoli Cell Tumor, Annular Tubular Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Sex Cord Tumor with Annular Tubules", "shortest_name_length": 35}
{"curie": "UMLS:C4525624", "names": ["Stage IV Ampulla of Vater Neuroendocrine Tumor", "Stage IV Ampulla of Vater Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Ampulla of Vater Neuroendocrine Tumor AJCC v8", "shortest_name_length": 46}
{"curie": "MONDO:0007752", "names": ["HYPERHEPARINEMIA", "hyperheparinemia", "Hyperheparinemia", "Hyperheparinaemia", "Hyperheparinemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperheparinemia", "shortest_name_length": 16}
{"curie": "UMLS:C5420543", "names": ["Metastatic Poorly Differentiated Thyroid Gland Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Poorly Differentiated Thyroid Gland Carcinoma", "shortest_name_length": 56}
{"curie": "UMLS:C0451981", "names": ["crush injury skull", "Crushing Skull Injury", "crush injury of skull", "Skull Injury, Crushing", "Crushing Skull Injuries", "crushing injury; cranium", "Crushing injury of skull", "Skull Injuries, Crushing", "cranium; crushing injury", "crush injury of skull (diagnosis)", "Crushing injury of skull (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Crushing Skull Injury", "shortest_name_length": 18}
{"curie": "MONDO:0044113", "names": ["BSLE", "systemic lupus erythematosus bullous", "Bullous systemic lupus erythematosus", "bullous systemic lupus erythematosus", "Bullous Systemic Lupus Erythematosus", "Bullous systemic lupus erythematosus (disorder)", "bullous systemic lupus erythematosus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bullous systemic lupus erythematosus", "shortest_name_length": 4}
{"curie": "MONDO:0010764", "names": ["DFNY1", "Y-linked deafness 1", "deafness, Y-linked 1", "DEAFNESS, Y-LINKED 1", "hearing loss, Y-linked 1", "deafness, y-linked 1, y-linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, Y-linked 1", "shortest_name_length": 5}
{"curie": "MONDO:0014122", "names": ["IMF2", "NOTCH3 myofibromatosis", "Infantile Myofibromatosis 2", "myofibromatosis, infantile 2", "MYOFIBROMATOSIS, INFANTILE, 2", "myofibromatosis, infantile, 2", "myofibromatosis, infantile, type 2", "myofibromatosis caused by mutation in NOTCH3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myofibromatosis, infantile, 2", "shortest_name_length": 4}
{"curie": "MONDO:0014908", "names": ["MCPH17", "primary autosomal recessive microcephaly 17", "CIT autosomal recessive primary microcephaly", "cit autosomal recessive primary microcephaly", "microcephaly 17, primary, autosomal recessive", "MICROCEPHALY 17, PRIMARY, AUTOSOMAL RECESSIVE", "microcephaly 17, primary, autosomal recessive; MCPH17", "autosomal recessive primary microcephaly caused by mutation in cit", "autosomal recessive primary microcephaly caused by mutation in CIT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly 17, primary, autosomal recessive", "shortest_name_length": 6}
{"curie": "MONDO:0033662", "names": ["NEDMISB", "neurodevelopmental disorder with microcephaly, seizures, and brain atrophy", "NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND BRAIN ATROPHY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with microcephaly, seizures, and brain atrophy", "shortest_name_length": 7}
{"curie": "MONDO:0014268", "names": ["IMD16", "OX40 DEFICIENCY", "OX40 deficiency", "IMMUNODEFICIENCY 16", "immunodeficiency 16", "immunodeficiency type 16", "Combined immunodeficiency due to OX40 deficiency", "combined immunodeficiency due to OX40 deficiency", "combined immunodeficiency with impaired immunity to HHV-8", "Combined immunodeficiency with impaired immunity to HHV-8", "Combined immunodeficiency due to OX40 deficiency (disorder)", "Combined immunodeficiency due to OX40 deficiency (diagnosis)", "combined immunodeficiency with childhood-onset Kaposi sarcoma", "Combined immunodeficiency with childhood-onset Kaposi sarcoma", "combined immunodeficiency with impaired immunity to human herpes virus 8", "Combined immunodeficiency with impaired immunity to human herpes virus 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined immunodeficiency due to OX40 deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0004844", "names": ["Leukokeratosis", "Leukokeratoses", "Oral Keratosis", "Oral Keratoses", "leukokeratosis", "Leucokeratosis", "oral keratosis", "oral keratoses", "Keratosis, Oral", "Keratoses, Oral", "Oral leucoplakia", "Oral leukoplakia", "Oral Leukoplakia", "Oral white patch", "leukoplakia oral", "ORAL LEUKOPLAKIA", "LEUKOPLAKIA ORAL", "Oral leukoplasia", "Leukoplakia oral", "Leukoplakia;oral", "oral leukoplakia", "Keratotic plaque", "leukoplakia mouth", "Mouth Leukoplakia", "leukoplakia, oral", "Oral white plaque", "Leukoplakia, Oral", "Oral Leukoplakias", "Leukoplakias, Oral", "mouth; leukoplakia", "Oral Leukokeratoses", "Oral Leukokeratosis", "Oral leukokeratosis", "Oral leukoplakia NOS", "Leukokeratosis, Oral", "Leukoplakia of mouth", "Leukoplakia of Mouth", "Leukoplakia oral NOS", "Leukokeratoses, Oral", "LEUKOPLAKIA OF MOUTH", "Leukoplakia buccalis", "oral mucosa leukoplakia", "Oral Cavity Leukoplakia", "Leukoplakia of the Mouth", "Leukokeratosis (disorder)", "Oral idiopathic keratosis", "leukoplakia of oral mucosa", "Leukoplakia of oral mucosa", "Leukoplakia of Oral Mucosa", "leukokeratosis (diagnosis)", "Leucoplakia of oral mucosa", "leukoplakia; buccal cavity", "Oral idiopathic leukoplakia", "Oral idiopathic white patch", "oral epithelium; leukoplakia", "leukoplakia; oral epithelium", "oral leukoplakia (diagnosis)", "leukokeratosis of oral mucosa", "Leukokeratosis of Oral Mucosa", "Leukokeratosis of oral mucosa", "leukoplakia of the oral mucosa", "Leukoplakia of the Oral Mucosa", "Leukoplakia of oral mucosa, NOS", "Leukoplakia of oral mucosa (disorder)", "Leukoplakia of oral mucosa, incl tongue", "Leukokeratosis (morphologic abnormality)", "erythroplakia; oral epithelium and tongue", "Leukoplakia of oral mucosa, including tongue", "Leukoplakia and other disturbances of oral epithelium, including tongue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oral mucosa leukoplakia", "shortest_name_length": 14}
{"curie": "MONDO:0012392", "names": ["SCAD", "SCADD", "ACADSD", "SBCADD", "SCAD deficiency", "Scad Deficiency", "SCAD DEFICIENCY", "Scadh Deficiency", "SBCAD deficiency", "SCADH DEFICIENCY", "ACADS deficiency", "ACADS DEFICIENCY", "Acads Deficiency", "2-MBCD Deficiency", "2-methylbutyric aciduria", "2-methylbutyrylglycinuria", "2-Methylbutyryl glycinuria", "2-Methylbutyryl Glycinuria", "2-METHYLBUTYRYL GLYCINURIA", "2-methylbutyryl Glycinuria", "Deficiency of butyryl dehydrogenase", "Butyryl-CoA Dehydrogenase Deficiency", "Butyryl-CoA dehydrogenase deficiency", "butyryl-CoA dehydrogenase deficiency", "Deficiency of Butyryl-Coa Dehydrogenase", "Deficiency of butyryl-CoA dehydrogenase", "2-Methylbutyryl-CoA Dehydrogenase Deficiency", "2-METHYLBUTYRYL-CoA DEHYDROGENASE DEFICIENCY", "2-methylbutyryl-CoA dehydrogenase deficiency", "Deficiency of unsaturated acyl-CoA reductase", "Short-chain acyl-CoA dehydrogenase deficiency", "2-@METHYLBUTYRYL-CoA DEHYDROGENASE DEFICIENCY", "Short-Chain Acyl-Coa Dehydrogenase Deficiency", "Short chain acyl-CoA dehydrogenase deficiency", "Short chain acyl CoA dehydrogenase deficiency", "Short chain Acyl CoA dehydrogenase deficiency", "short-chain acyl-CoA dehydrogenase deficiency", "Acyl-CoA Dehydrogenase, Short-Chain Deficiency", "Deficiency of 2-methylbutyryl-CoA dehydrogenase", "Acyl-Coa Dehydrogenase, Short-Chain, Deficiency Of", "ACYL-CoA DEHYDROGENASE, SHORT-CHAIN, DEFICIENCY OF", "Deficiency of butyryl-CoA dehydrogenase (disorder)", "2-Methylbutyryl-Coenzyme A Dehydrogenase Deficiency", "SCAD - Short chain acyl-CoA dehydrogenase deficiency", "Short-chain acyl-coenzyme A dehydrogenase deficiency", "Short-Chain Acyl-CoA Dehydrogenase Deficiency (SCAD)", "Short chain acyl CoA dehydrogenase deficiency (SCAD)", "SCAD - short chain acyl-CoA dehydrogenase deficiency", "Short-Chain Acyl-Coenzyme A Dehydrogenase Deficiency", "Short chain acyl-coenzyme A dehydrogenase deficiency", "short branched-chain acyl-CoA dehydrogenase deficiency", "Deficiency of 2-methylbutyryl-coenzyme A dehydrogenase", "short/branched-chain acyl-Coa dehydrogenase deficiency", "Short/branched-chain acyl-coA dehydrogenase deficiency", "Short-Branched-Chain Acyl-CoA Dehydrogenase Deficiency", "short/branched-chain acyl-coA dehydrogenase deficiency", "SHORT/BRANCHED-CHAIN ACYL-CoA DEHYDROGENASE DEFICIENCY", "short-chain acyl-CoA dehydrogenase deficiency (diagnosis)", "Short-Chain Acyl-Coenzyme A Dehydrogenase Deficiency (SCAD)", "ACADS - short chain acyl-coenzyme A dehydrogenase deficiency", "Short chain acyl-coenzyme A dehydrogenase deficiency (disorder)", "Deficiency of 2-methylbutyryl-coenzyme A dehydrogenase (disorder)", "developmental delay due to 2-methylbutyryl-CoA dehydrogenase deficiency", "Developmental delay due to 2-methylbutyryl-CoA dehydrogenase deficiency", "Lipid-Storage Myopathy Secondary to Short-Chain Acyl-Coa Dehydrogenase Deficiency", "LIPID-STORAGE MYOPATHY SECONDARY TO SHORT-CHAIN ACYL-CoA DEHYDROGENASE DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "2-methylbutyryl-CoA dehydrogenase deficiency", "shortest_name_length": 4}
{"curie": "UMLS:C0266527", "names": ["eye; hypoplasia", "hypoplasia; eye", "Rudimentary eye", "rudimentary; eye", "eye; rudimentary", "Hypoplasia of eye", "congenital rudimentary eye", "congenital hypoplasia of eye", "Hypoplasia of eye (disorder)", "congenital rudimentary eye (diagnosis)", "congenital hypoplasia of eye (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypoplasia of eye", "shortest_name_length": 15}
{"curie": "MONDO:0024884", "names": ["Carcinoma bone", "carcinoma bone", "bone carcinoma", "CARCINOMA BONE", "Carcinoma;bone(s)", "carcinoma of the bone(s)", "Metastatic Carcinoma in the Bone", "metastatic carcinoma to the bone", "metastatic carcinoma in the bone", "Metastatic Carcinoma to the Bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metastatic carcinoma in the bone", "shortest_name_length": 14}
{"curie": "MONDO:0019522", "names": ["RDEB-O", "RDEB-generalized other", "generalized mitis RDEB", "RDEB generalisata mitis", "RDEB, generalized intermediate", "RDEB, non-Hallopeau-Siemens type", "recessive dystrophic epidermolysis bullosa-generalized other", "recessive dystrophic epidermolysis bullosa, generalized intermediate", "recessive dystrophic epidermolysis bullosa, non-Hallopeau-Siemens type", "autosomal recessive dystrophic epidermolysis bullosa, generalized other", "autosomal recessive dystrophic epidermolysis bullosa generalisata mitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "recessive dystrophic epidermolysis bullosa-generalized other", "shortest_name_length": 6}
{"curie": "MONDO:0018376", "names": ["secondary non-traumatic AVN", "secondary non-traumatic avascular necrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary non-traumatic avascular necrosis", "shortest_name_length": 27}
{"curie": "MONDO:0015682", "names": ["primary peritoneal tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary peritoneal tumor", "shortest_name_length": 24}
{"curie": "UMLS:C4553417", "names": ["stage III adrenocortical cancer", "Stage III Adrenal Cortex Cancer", "stage III adrenal cortex carcinoma", "stage III adrenocortical carcinoma", "carcinoma, adrenocortical stage III", "adrenocortical carcinoma, stage III", "Stage III Adrenal Cortex Carcinoma AJCC v8", "stage III adrenal cortex carcinoma AJCC v8", "Stage III Adrenal Cortical Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Adrenal Cortex Carcinoma AJCC v8", "shortest_name_length": 31}
{"curie": "MONDO:0009176", "names": ["EV", "ever", "Lutz Lewandowsky Disease", "Lutz-Lewandowsky Disease", "Lewandowsky-Lutz disease", "Lewandowsky Lutz Disease", "Lewandowsky-Lutz Disease", "Disease, Lewandowsky-Lutz", "Disease, Lutz-Lewandowsky", "Lewandowsky-Lutz syndrome", "Lewandowsky-Lutz Dysplasia", "Lewandowsky-Lutz dysplasia", "EPIDERMODYSPLASIA VERRUCIFORMIS", "epidermodysplasia verruciformis", "Epidermodysplasia verruciformis", "Epidermodysplasia Verruciformis", "Epidermodysplasia verruciformis (disorder)", "epidermodysplasia verruciformis (diagnosis)", "Lutz-Lewandowsky epidermodysplasia verruciformis", "Epidermodysplasia verruciformis of Lewandowsky-Lutz"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermodysplasia verruciformis", "shortest_name_length": 2}
{"curie": "UMLS:C1710248", "names": ["Sunset Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sunset Syndrome", "shortest_name_length": 15}
{"curie": "UMLS:C1516429", "names": ["Cervical Papillary Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Papillary Squamous Cell Carcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0000964", "names": ["lipoma skin", "Lipoma;skin", "skin lipoma", "Skin Lipoma", "lipoma; skin", "skin; lipoma", "lipoma of skin", "Lipoma of Skin", "lipoma of face", "Lipoma of skin", "cutaneous lipoma", "Cutaneous Lipoma", "lipoma of the skin", "Lipoma of the Skin", "zone of skin lipoma", "Lipomatous Skin Tumor", "lipoma of zone of skin", "Lipomatous Skin Neoplasm", "Skin Lipomatous Neoplasm", "Lipomatous Tumor of Skin", "Lipoma of skin (disorder)", "Cutaneous Lipomatous Tumor", "cutaneous lipomatous tumor", "lipoma of skin (diagnosis)", "Lipomatous Neoplasm of Skin", "Lipomatous Tumor of the Skin", "Cutaneous Lipomatous Neoplasm", "Lipomatous Neoplasm of the Skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin lipoma", "shortest_name_length": 11}
{"curie": "UMLS:C1883045", "names": ["Small congenital nevus", "Small Congenital Melanocytic Nevus", "Congenital small melanocytic nevus", "Congenital small melanocytic naevus", "Congenital small melanocytic nevus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital small melanocytic nevus", "shortest_name_length": 22}
{"curie": "UMLS:C1335694", "names": ["Recurrent Bone Ewing Sarcoma", "Relapsed Bone Ewing's Sarcoma", "Recurrent Bone Ewing's Sarcoma", "Relapsed Osseous Ewing's Sarcoma", "Relapsed Ewing's Sarcoma of Bone", "Recurrent Ewing's Sarcoma of Bone", "Relapsed Skeletal Ewing's Sarcoma", "Recurrent Osseous Ewing's Sarcoma", "Recurrent Skeletal Ewing's Sarcoma", "Relapsed Ewing's Sarcoma of the Bone", "Recurrent Ewing's Sarcoma of the Bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Bone Ewing Sarcoma", "shortest_name_length": 28}
{"curie": "UMLS:C0009075", "names": ["Cloudman S91 Melanoma", "S91 Melanoma, Cloudman", "Melanoma, Cloudman S91", "Cloudman S91 Malignant Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Melanoma, Cloudman S91", "shortest_name_length": 21}
{"curie": "MONDO:0011516", "names": ["Erni", "early response to neural induction gene"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early response to neural induction gene", "shortest_name_length": 4}
{"curie": "OMIM:179620", "names": [], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"]}
{"curie": "MONDO:0003165", "names": ["cerebellum astrocytoma", "Cerebellar astrocytoma", "cerebellar astrocytoma", "Cerebellar Astrocytoma", "CEREBELLAR ASTROCYTOMA", "astrocytoma, cerebellar", "Astrocytoma, Cerebellar", "astrocytoma of Cerebellum", "Astrocytoma of Cerebellum", "astrocytoma of cerebellum", "astrocytoma of the cerebellum", "Astrocytoma of the Cerebellum", "cerebellum astrocytoma (excluding glioblastoma)", "astrocytoma (excluding glioblastoma) of cerebellum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellar astrocytoma", "shortest_name_length": 22}
{"curie": "MONDO:0035879", "names": ["granuloma faciale", "Granuloma of Lever", "Facial granuloma of Lever"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "granuloma faciale", "shortest_name_length": 17}
{"curie": "UMLS:C2827583", "names": ["Selective Antibody Deficiency with Normal Immunoglobulins"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Selective Antibody Deficiency with Normal Immunoglobulins", "shortest_name_length": 57}
{"curie": "UMLS:C1334610", "names": ["Malignant Parotid Mixed Tumor", "Malignant Parotid Mixed Neoplasm", "Malignant Mixed Tumor of Parotid", "Malignant Mixed Neoplasm of Parotid", "Malignant Parotid Gland Mixed Tumor", "Malignant Mixed Tumor of the Parotid", "Malignant Parotid Gland Mixed Neoplasm", "Malignant Mixed Tumor of Parotid Gland", "Malignant Mixed Neoplasm of the Parotid", "Malignant Mixed Neoplasm of Parotid Gland", "Malignant Mixed Tumor of the Parotid Gland", "Malignant Mixed Neoplasm of the Parotid Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Parotid Gland Mixed Tumor", "shortest_name_length": 29}
{"curie": "MONDO:0012289", "names": ["MFM5", "filaminopathy", "muscle filaminopathy", "Mfm, Filamin C-Related", "myofibrillar myopathy 5", "MYOPATHY, MYOFIBRILLAR, 5", "myopathy, myofibrillar, 5", "myofibrillar myopathy type 5", "myopathy, myofibrillar, type 5", "Filaminopathy, autosomal dominant", "FILAMINOPATHY, AUTOSOMAL DOMINANT", "filaminopathy, autosomal dominant", "FLNC myofibrillar myopathy (disease)", "Filamin C-related myofibrillar myopathy", "Myofibrillar myopathy, filamin C-related", "myopathy, myofibrillar, filamin C-related", "MYOPATHY, MYOFIBRILLAR, FILAMIN C-RELATED", "Myopathy, Myofibrillar, Filamin C-Related", "myofibrillar myopathy (disease) caused by mutation in FLNC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myofibrillar myopathy 5", "shortest_name_length": 4}
{"curie": "MONDO:0009173", "names": ["enterokinase deficiency", "Enterokinase Deficiency", "ENTEROKINASE DEFICIENCY", "Deficiency of enterokinase", "ENTEROPEPTIDASE DEFICIENCY", "enteropeptidase deficiency", "Enteropeptidase Deficiency", "deficiency of enteropeptidase", "Deficiency of enteropeptidase", "Enterokinase deficiency disease", "Intestinal enterokinase deficiency", "Congenital enterokinase deficiency", "congenital enterokinase deficiency", "Intestinal enteropeptidase deficiency", "Deficiency of enteropeptidase (disorder)", "Intestinal pseudo-trypsinogen deficiency", "Intestinal enteropeptidase deficiency (disorder)", "Intestinal enteropeptidase deficiency (diagnosis)", "Congenital enteropathy due to enteropeptidase deficiency", "congenital enteropathy due to enteropeptidase deficiency", "malabsorption syndrome intestinal enteropeptidase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital enteropathy due to enteropeptidase deficiency", "shortest_name_length": 23}
{"curie": "UMLS:C3273075", "names": ["Liver Synovial Sarcoma", "Hepatic Synovial Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liver Synovial Sarcoma", "shortest_name_length": 22}
{"curie": "MONDO:0017173", "names": ["non-syndromic male infertility due asthenozoospermia", "isolated male infertility due to sperm motility disorder", "nonsyndromic male infertility due to sperm motility disorder", "non-syndromic male infertility due to sperm motility disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-syndromic male infertility due to sperm motility disorder", "shortest_name_length": 52}
{"curie": "MONDO:0035009", "names": ["isolated mesenteric vein thrombosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated mesenteric vein thrombosis", "shortest_name_length": 35}
{"curie": "MONDO:0009366", "names": ["NPH", "nph", "HYDNP1", "Hakim Syndrome", "hakim syndrome", "Syndrome, Hakim", "Hakim Syndromes", "Hakims Syndrome", "Hakim's Syndrome", "Syndromes, Hakim", "Hakim's Syndromes", "Syndrome, Hakim's", "Syndromes, Hakim's", "low pressure hydrocephalus", "Low pressure hydrocephalus", "chronic adult hydrocephalus", "Hydrocephalus, low pressure", "Normal pressure hydrocephaly", "normal pressure hydrocephaly", "NORMAL PRESSURE HYDROCEPHALY", "Normal-pressure hydrocephalus", "HYDROCEPHALUS NORMAL PRESSURE", "hydrocephalus normal pressure", "Normal pressure hydrocephalus", "hydrocephalus pressure normal", "normal-pressure hydrocephalus", "Normal Pressure Hydrocephalus", "normal pressure hydrocephalus", "NORMAL PRESSURE HYDROCEPHALUS", "hydrocephalus; normal-pressure", "Hydrocephalus, Normal Pressure", "Hydrocephalus, Normal-Pressure", "normal-pressure; hydrocephalus", "Hydrocephalus, normal pressure", "hydrocephalus, normal-pressure", "HYDROCEPHALUS, NORMAL PRESSURE, 1", "HYDROCEPHALUS, NORMAL-PRESSURE, 1", "Normal pressure hydrocephalus NOS", "hydrocephalus, normal pressure, 1", "hydrocephalus normal nph pressure", "NPH (normal pressure hydrocephalus)", "NPH (Normal Pressure Hydrocephalus)", "normal pressure hydrocephalus (nph)", "NPH - Normal pressure hydrocephalus", "NPHs (Normal Pressure Hydrocephalus)", "Normal pressure hydrocephalus syndrome", "Normal pressure hydrocephalus (disorder)", "normal pressure hydrocephalus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "normal pressure hydrocephalus", "shortest_name_length": 3}
{"curie": "UMLS:C5555863", "names": ["Locally Advanced Chromophobe Renal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Chromophobe Renal Cell Carcinoma", "shortest_name_length": 49}
{"curie": "UMLS:C0234529", "names": ["Dressing Apraxia", "Dressing apraxia", "dressing apraxia", "Dressing Apraxias", "Apraxia, Dressing", "Apraxias, Dressing", "Apraxia of dressing", "dressing apraxia was noted", "Apraxia of dressing (finding)", "dressing apraxia (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dressing Apraxia", "shortest_name_length": 16}
{"curie": "MONDO:0044325", "names": ["FANCW", "FANCONI ANEMIA, COMPLEMENTATION GROUP W", "Fanconi anemia, complementation group W"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fanconi anemia, complementation group W", "shortest_name_length": 5}
{"curie": "UMLS:C2987519", "names": ["Stage II Cervical Cancer", "Stage II Cervical Cancer AJCC v7", "Cervical carcinoma stage II AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical carcinoma stage II AJCC v7", "shortest_name_length": 24}
{"curie": "UMLS:C4763712", "names": ["AIN1", "LG-AIN", "Anal Intraepithelial Neoplasia 1", "Low Grade Anal Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Grade Anal Intraepithelial Neoplasia", "shortest_name_length": 4}
{"curie": "UMLS:C1711312", "names": ["Breast Carcinoma with Osseous Metaplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Carcinoma with Osseous Metaplasia", "shortest_name_length": 40}
{"curie": "UMLS:C4053745", "names": ["Calcineurin Inhibitor - Induced Nephropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Calcineurin Inhibitor - Induced Nephropathy", "shortest_name_length": 43}
{"curie": "OMIM:615264", "names": ["VEL-NULL PHENOTYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 18}
{"curie": "MONDO:0012204", "names": ["PSHK2", "cryohydrocytosis, mild", "CRYOHYDROCYTOSIS, MILD", "Pseudohyperkalemia Lille", "PSEUDOHYPERKALEMIA LILLE", "pseudohyperkalemia Lille", "PSEUDOHYPERKALEMIA FALKIRK", "pseudohyperkalemia Falkirk", "PSEUDOHYPERKALEMIA CHISWICK", "pseudohyperkalemia Chiswick", "familial pseudohyperkalemia", "Familial pseudohyperkalemia", "Familial pseudohyperkalaemia", "pseudohyperkalemia East London", "PSEUDOHYPERKALEMIA EAST LONDON", "Familial pseudohyperkalemia (disorder)", "Pseudohyperkalemia, Familial, 2, due to Red Cell Leak", "PSEUDOHYPERKALEMIA, FAMILIAL, 2, DUE TO RED CELL LEAK", "pseudohyperkalemia, familial, 2, due to red cell leak"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial pseudohyperkalemia", "shortest_name_length": 5}
{"curie": "MONDO:0030513", "names": ["DYT33", "dystonia 33", "DYSTONIA 33"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dystonia 33", "shortest_name_length": 5}
{"curie": "UMLS:C1739389", "names": ["Urachal remnant", "Urachal Remnant", "urachus; remnant", "remnant; urachus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urachal remnant", "shortest_name_length": 15}
{"curie": "MONDO:0011872", "names": ["GS2", "PAID Syndrome", "Paid syndrome", "PAID syndrome", "PAID SYNDROME", "Griscelli disease type 2", "Griscelli Syndrome Type 2", "Griscelli syndrome type 2", "GRISCELLI SYNDROME, TYPE 2", "Griscelli syndrome, type 2", "Griscelli Syndrome, Type 2", "Griscelli-Prunieras syndrome type 2", "Griscelli-Pruniéras syndrome type 2", "Griscelli-Pruni��ras syndrome type 2", "Griscelli-PruniC)ras syndrome type 2", "Partial albinism and immunodeficiency", "Albinism, partial with immunodeficiency", "PARTIAL ALBINISM AND IMMUNODEFICIENCY SYNDROME", "Partial Albinism and Immunodeficiency Syndrome", "Partial Albinism And Immunodeficiency Syndrome", "partial albinism and immunodeficiency syndrome", "GRISCELLI SYNDROME WITH HEMOPHAGOCYTIC SYNDROME", "Griscelli syndrome with hemophagocytic syndrome", "hypopigmentation-immunodeficiency with or without neurologic impairment syndrome", "Hypopigmentation-immunodeficiency with or without neurologic impairment syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Griscelli syndrome type 2", "shortest_name_length": 3}
{"curie": "MONDO:0008547", "names": ["TD2", "thanatophoric dwarfism type 2", "Thanatophoric dwarfism type 2", "Thanatophoric dysplasia type 2", "type 2 thanatophoric dysplasia", "thanatophoric dysplasia type 2", "Type 2 Thanatophoric Dysplasia", "Thanatophoric dysplasia, type 2", "Thanatophoric Dysplasia, Type 2", "thanatophoric dysplasia type II", "thanatophoric dysplasia, type 2", "Thanatophoric Dysplasia, Type Ii", "THANATOPHORIC DYSPLASIA, TYPE II", "thanatophoric dysplasia, type II", "thanatophoric dwarfism - cloverleaf skull", "Thanatophoric dysplasia, type 2 (disorder)", "Cloverleaf skull with thanatophoric dwarfism", "CLOVERLEAF SKULL WITH THANATOPHORIC DWARFISM", "cloverleaf skull with thanatophoric dwarfism", "THANATOPHORIC DYSPLASIA WITH KLEEBLATTSCHAEDEL", "thanatophoric dysplasia with Kleeblattschaedel", "Thanatophoric dysplasia with Kleeblattschaedel", "Thanatophoric dwarfism-cloverleaf skull syndrome", "thanatophoric dwarfism-cloverleaf skull syndrome", "cloverleaf skull-micromelic bone dysplasia syndrome", "Cloverleaf skull-micromelic bone dysplasia syndrome", "Thanatophoric Dysplasia With Straight Femurs And Cloverleaf Skull", "thanatophoric dysplasia with straight femurs and cloverleaf skull", "THANATOPHORIC DYSPLASIA WITH STRAIGHT FEMURS AND CLOVERLEAF SKULL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thanatophoric dysplasia type 2", "shortest_name_length": 3}
{"curie": "EFO:0009784", "names": ["central serous retinopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central serous retinopathy", "shortest_name_length": 26}
{"curie": "MONDO:0000922", "names": ["PID", "pid", "P.I.D.", "Pelvic infection", "Pelvic Infection", "pelvic infection", "Inflammation pelvic", "pelvic inflammation", "Pelvic inflammation", "INFLAMMATION PELVIC", "PELVIC INFLAMMATION", "inflammation; pelvic", "Female pelvic inflammation", "PELVIC INFLAMMATORY DISEASE", "Pelvic inflammatory disease", "Disease;pelvic inflammatory", "Pelvic Inflammatory Disease", "DISEASE PELVIC INFLAMMATORY", "Inflammatory Pelvic Disease", "Disease pelvic inflammatory", "inflammatory pelvic disease", "pelvic inflammatory disease", "Inflammatory Pelvic Diseases", "Pelvic Disease, Inflammatory", "Inflammatory Disease, Pelvic", "Disease, Inflammatory Pelvic", "Pelvic Inflammatory Diseases", "Disease, Pelvic Inflammatory", "pelvic inflammatory diseases", "Diseases, Inflammatory Pelvic", "pelvic inflammatory infection", "Diseases, Pelvic Inflammatory", "Infection;pelvic inflammatory", "Inflammatory Diseases, Pelvic", "Pelvic Diseases, Inflammatory", "PID Pelvic inflammatory disease", "Pelvic inflammatory disease NOS", "PID, pelvic inflammatory disease", "PID - pelvic inflammatory disease", "Pelvic inflammatory disease (PID)", "pelvic inflammatory disease (PID)", "disease (PID), pelvic inflammatory", "inflammatory disease (PID), pelvic", "pelvic inflammatory disease, (PID)", "Female pelvic inflammatory disease", "pelvic inflammatory disease; female", "pelvic inflammatory disease (diagnosis)", "INFLAMMATORY DISEASE OF FEMALE PELVIC ORGANS", "Inflammatory diseases of female pelvic organs", "Female pelvic inflammatory disease (disorder)", "Female pelvic inflammatory disease, unspecified", "Inflammatory diseases of female pelvic organs (N70-N77)", "Inflammatory disease of female pelvic organs and tissues, NOS", "INFLAMMATORY DISEASES OF THE FEMALE GENITAL ORGANS AND TISSUES", "Unspecified inflammatory disease of female pelvic organs and tissues"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pelvic inflammatory disease", "shortest_name_length": 3}
{"curie": "MONDO:0018947", "names": ["CNM", "myotubular myopathy", "myopathy myotubular", "Myotubular myopathy", "myopathy; myotubular", "myopathy, myotubular", "myotubular; myopathy", "Centronuclear myopathy", "Centronuclear Myopathy", "centronuclear myopathy", "Myopathy, Centronuclear", "myopathy; centronuclear", "centronuclear; myopathy", "myopathy, centronuclear", "Centronuclear Myopathies", "Myopathies, Centronuclear", "Centronuclear myopathy, NOS", "centronuclear myopathy (CNM)", "Myotubular myopathy (disorder)", "myotubular myopathy (diagnosis)", "centronuclear myopathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "centronuclear myopathy", "shortest_name_length": 3}
{"curie": "MONDO:0012751", "names": ["AAA3", "Aaa3", "aneurysm, familial abdominal 3", "Aortic Aneurysm, Familial Abdominal 3", "aortic aneurysm, familial abdominal, 3", "AORTIC ANEURYSM, FAMILIAL ABDOMINAL, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic aneurysm, familial abdominal, 3", "shortest_name_length": 4}
{"curie": "UMLS:C0393671", "names": ["Benign Frontal Childhood Epilepsy", "Childhood Benign Frontal Epilepsy", "Frontal Epilepsy, Benign, Childhood", "Epilepsy, Benign Frontal, Childhood", "Benign frontal epilepsy of childhood", "Benign frontal epilepsy of childhood (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Frontal Epilepsy, Benign, Childhood", "shortest_name_length": 33}
{"curie": "UMLS:C0242707", "names": ["Right ventricular dysfunction", "Right Ventricular Dysfunction", "Ventricular Dysfunction, Right", "Right Ventricular Dysfunctions", "Dysfunction, Right Ventricular", "Ventricular Dysfunctions, Right", "Dysfunctions, Right Ventricular"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Right Ventricular Dysfunction", "shortest_name_length": 29}
{"curie": "UMLS:C3544106", "names": ["Hyperammonemic crisis", "Hyperammonaemic crisis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyperammonaemic crisis", "shortest_name_length": 21}
{"curie": "UMLS:C0521659", "names": ["UMN disease", "disease motor neuron upper", "Upper Motor Neuron Disease", "Upper motor neuron disease", "upper motor neuron disease", "UPPER MOTOR NEURON DISEASE", "Motor Neuron Disease, Upper", "diseases motor neuron upper", "Upper motor neuron disease, NOS", "Upper motor neuron disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Motor Neuron Disease, Upper", "shortest_name_length": 11}
{"curie": "MONDO:0035694", "names": ["CID due to RELA haploinsufficiency", "combined immunodeficiency due to RELA haploinsufficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined immunodeficiency due to RELA haploinsufficiency", "shortest_name_length": 34}
{"curie": "UMLS:C2981667", "names": ["stage IIB distal bile duct cancer", "Stage IIB Distal Bile Duct Cancer", "stage IIB distal bile duct cancer AJCC v7", "Stage IIB Distal Bile Duct Cancer AJCC v7", "stage IIB distal extrahepatic bile duct cancer", "Stage IIB Extrahepatic (Distal) Bile Duct Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Distal Bile Duct Cancer AJCC v7", "shortest_name_length": 33}
{"curie": "UMLS:C0019489", "names": ["Hexosediphosphatase Deficiency", "Deficiency, Hexosediphosphatase", "Hexosediphosphatase Deficiencies", "Deficiency of hexosediphosphatase", "Deficiencies, Hexosediphosphatase", "Deficiency of fructose-bisphosphatase", "Deficiency of fructose-bisphosphatase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Deficiency, Hexosediphosphatase", "shortest_name_length": 30}
{"curie": "MONDO:0006899", "names": ["operculitis", "Operculitis", "Pericoronitis", "pericoronitis", "Pericoronitides", "Pericoronitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pericoronitis", "shortest_name_length": 11}
{"curie": "MONDO:0023111", "names": ["familial capillaro-venous leptomeningeal angiomatosis", "Familial capillaro-venous leptomeningeal angiomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial capillaro-venous leptomeningeal angiomatosis", "shortest_name_length": 53}
{"curie": "UMLS:C4744390", "names": ["Sellar Choriocarcinoma", "Choriocarcinoma of the Sellar Region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sellar Choriocarcinoma", "shortest_name_length": 22}
{"curie": "UMLS:C4683558", "names": ["Hodgkin Lymphoma by Ann Arbor Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin Lymphoma by Ann Arbor Stage", "shortest_name_length": 35}
{"curie": "MONDO:0008710", "names": ["CRPT1", "ACPS 2", "Carpenter syndrome", "CARPENTER syndrome 1", "Carpenter syndrome 1", "CARPENTER SYNDROME 1", "Carpenter syndrome-1", "RAB23 Carpenter syndrome", "Carpenter syndrome type 1", "acrocephalopolysyndactyly type 2", "RAB23-related Carpenter syndrome", "Carpenter syndrome caused by mutation in RAB23"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "RAB23-related Carpenter syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0015767", "names": ["trisomy 4p", "4p trisomy", "Duplication 4p", "4p duplication", "trisomy type 4p", "partial trisomy 4p", "Duplication 4p Syndrome", "chromosome 4p duplication", "trisomy of the short arm of chromosome 4", "Duplication of the short arm of chromosome 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trisomy 4p", "shortest_name_length": 10}
{"curie": "MONDO:0012365", "names": ["GBD2", "Gallbladder Disease 2", "gallbladder disease 2", "GALLBLADDER DISEASE 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gallbladder disease 2", "shortest_name_length": 4}
{"curie": "UMLS:C0274702", "names": ["SYNDROME CHOLINERGIC", "Syndrome cholinergic", "Cholinergic syndrome", "CHOLINERGIC SYNDROME", "Cholinergic poisoning", "Poisoning by cholinergics", "parasympathomimetic toxicity", "Parasympathomimetic syndrome", "PARASYMPATHOMIMETIC SYNDROME", "SYNDROME PARASYMPATHOMIMETIC", "Syndrome parasympathomimetic", "Poisoning by cholinergic drug", "Parasympathomimetic poisoning", "Poisoning by parasympathomimetics", "Poisoning by cholinergic drug, NOS", "Poisoning caused by cholinergic drug", "Poisoning by parasympathomimetic drug", "parasympathomimetic toxicity (diagnosis)", "Poisoning by parasympathomimetic drug, NOS", "Poisoning caused by parasympathomimetic drug", "Poisoning by parasympathomimetics (cholinergics)", "Poisoning caused by parasympathomimetic drug (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Poisoning by parasympathomimetic drug", "shortest_name_length": 20}
{"curie": "UMLS:C5237398", "names": ["Invasive Bladder Mixed Carcinoma", "Infiltrating Bladder Mixed Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infiltrating Bladder Mixed Carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0010120", "names": ["THC3", "Thrombocytopenia 3", "THROMBOCYTOPENIA 3", "thrombocytopenia 3", "Thrombocytopenia, Autosomal Recessive, 3", "THROMBOCYTOPENIA, AUTOSOMAL RECESSIVE, 3", "thrombocytopenia, autosomal recessive, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombocytopenia 3", "shortest_name_length": 4}
{"curie": "MONDO:0016445", "names": ["Familial anetoderma", "familial anetoderma", "Hereditary anetoderma", "hereditary anetoderma", "hereditary macular atrophy", "Hereditary macular atrophy", "Hereditary anetoderma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial anetoderma", "shortest_name_length": 19}
{"curie": "MONDO:8000002", "names": ["escherichia coli discitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "escherichia coli discitis", "shortest_name_length": 25}
{"curie": "EFO:0600032", "names": ["congenital right-sided heart lesions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital right-sided heart lesions", "shortest_name_length": 36}
{"curie": "MONDO:0020480", "names": ["MOCOD", "molybdenum cofactor deficiency", "sulfite oxidase deficiency due to molybdenum cofactor deficiency", "combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase", "combined deficiency of sulfite oxidase, xanthine dehydrogenase, and aldehyde oxidase"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sulfite oxidase deficiency due to molybdenum cofactor deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0006922", "names": ["Mycoplasmal anemia", "Haemobartonelloses", "Haemobartonellosis", "Mycoplasmal anaemia", "Anaplasmataceae Infection", "Anaplasmataceae infection", "infection, Anaplasmataceae", "Infection, Anaplasmataceae", "Anaplasmataceae Infections", "infections, Anaplasmataceae", "Infections, Anaplasmataceae", "Mycoplasmal anemia (disorder)", "Anaplasmataceae infectious disease", "Anaplasmataceae disease or disorder", "primary Anaplasmataceae infectious disease", "Anaplasmataceae caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anaplasmataceae infectious disease", "shortest_name_length": 18}
{"curie": "MONDO:0018116", "names": ["galactosemia", "Galactosemia", "GALACTOSEMIA", "galactosaemia", "Galactosemias", "galactosemias", "Galactosaemia", "Hypergalactosemia", "Galactosemia, NOS", "Galactosaemia, NOS", "Galactose intolerance", "galactose intolerance", "GALACTOSE INTOLERANCE", "disorder galactosemia", "Galactosemia (disorder)", "galactosemia (diagnosis)", "Galactose intolerance, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "galactosemia", "shortest_name_length": 12}
{"curie": "MONDO:0013374", "names": ["supernumerary der(22)t(8;22) syndrome", "supernumerary der(22)t(8-22) syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "supernumerary der(22)t(8;22) syndrome", "shortest_name_length": 37}
{"curie": "MONDO:0008378", "names": ["RP9", "RP 9", "Retinitis Pigmentosa 9", "RETINITIS PIGMENTOSA 9", "retinitis pigmentosa 9", "RP9 retinitis pigmentosa", "retinitis pigmentosa type 9", "retinitis pigmentosa caused by mutation in RP9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 9", "shortest_name_length": 3}
{"curie": "MONDO:0010225", "names": ["XRN", "NPHL1", "NPHL2", "Nphl2", "DENT1", "Dent disease 1", "DENT disease 1", "DENT DISEASE 1", "nephrolithiasis 2", "NEPHROLITHIASIS 2", "Nephrolithiasis 2", "nephrolithiasis 1", "CLCN5 Dent disease", "Dent disease type 1", "nephrolithiasis type 1", "Dent disease type 1 (disorder)", "X-linked nephrolithiasis type I", "dent disease 1, X-linked recessive", "X-linked recessive urolithiasis type 1", "urolithiasis, hypercalciuric, X-linked", "UROLITHIASIS, HYPERCALCIURIC, X-LINKED", "Urolithiasis, Hypercalciuric, X-Linked", "Dent disease caused by mutation in CLCN5", "Nephrolithiasis, Hypercalciuric, X-Linked", "nephrolithiasis X-linked recessive type 1", "NEPHROLITHIASIS, HYPERCALCIURIC, X-LINKED", "Nephrolithiasis, hypercalciuria, x-linked", "nephrolithiasis, hypercalciuric, X-linked", "X-linked nephrolithiasis with renal failure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dent disease type 1", "shortest_name_length": 3}
{"curie": "MONDO:0008964", "names": ["CLD", "DIAR1", "Darrow-gamble disease", "Darrow-Gamble disease", "Congenital chloridorrhea", "congenital chloridorrhea", "Chloridorrhea, congenital", "Congenital chloridorrhoea", "CHLORIDORRHEA, CONGENITAL", "SLC26A3 secretory diarrhea", "familial chloride diarrhea", "Congenital chloride diarrhea", "congenital chloride diarrhea", "Congenital chloride diarrhoea", "congenital secretory chloride diarrhea 1", "congenital chloride diarrhea finnish type", "congenital chloride diarrhea Finnish type", "congenital secretory chloride diarrhoea 1", "congenital chloride diarrhoea finnish type", "Diarrhea 1, secretory chloride, congenital", "DIARRHEA 1, SECRETORY CHLORIDE, CONGENITAL", "diarrhea 1, secretory chloride, congenital", "CHLORIDE DIARRHEA, CONGENITAL, FINNISH TYPE", "chloride diarrhea, congenital, Finnish type", "Congenital secretory diarrhea, chloride type", "Congenital secretory diarrhoea, chloride type", "congenital secretory chloride diarrhea type 1", "Defective Cl-/HCO-3 exchange in ileum and colon", "secretory diarrhea caused by mutation in SLC26A3", "Defective Cl-/HCO-3 exchange in ileum AND/OR colon", "Congenital secretory diarrhea, chloride type (disorder)", "Defective Cl^-^/HCO^-^>3< exchange in ileum AND/OR colon", "Defective Cl<sup>-</sup>/HCO<sup>-</sup><sub>3</sub> exchange in ileum AND/OR colon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital secretory chloride diarrhea 1", "shortest_name_length": 3}
{"curie": "UMLS:C0349734", "names": ["Cellulitis;pelvis;F", "Female pelvic cellulitis", "Pelvic cellulitis, female", "cellulitis of the female pelvis", "Female pelvic cellulitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Female pelvic cellulitis", "shortest_name_length": 19}
{"curie": "MONDO:0018048", "names": ["HIT", "HAT", "Heparin-Induced Thrombocytopenia", "heparin-induced thrombocytopenia", "Heparin-induced thrombocytopenia", "Heparin induced thrombocytopenia", "heparin induced thrombocytopenia", "HEPARIN INDUCED THROMBOCYTOPENIA", "Heparin Induced Thrombocytopenia", "Heparin induced thrombocytopaenia", "Heparin-associated thrombocytopenia", "heparin-associated thrombocytopenia", "Heparin-induced thrombocytopenia NOS", "Heparin-induced thrombocytopenia (HIT)", "Heparin induced thrombocytopenia (HIT)", "Heparin-induced thrombocytopenia type 2", "heparin-induced thrombocytopenia type 2", "heparin-induced thrombocytopenia (disease)", "Heparin-induced thrombocytopenia (disorder)", "heparin-induced thrombocytopenia (diagnosis)", "Heparin-induced thrombocytopenia, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heparin-induced thrombocytopenia", "shortest_name_length": 3}
{"curie": "MONDO:0015214", "names": ["syndromic visceral malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic visceral malformation", "shortest_name_length": 31}
{"curie": "UMLS:C1335729", "names": ["Refractory tumor", "Refractory Tumor", "Refractory Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Neoplasm", "shortest_name_length": 16}
{"curie": "MONDO:0001957", "names": ["Critical illness polyneuropathy", "Critical Illness Polyneuropathy", "critical illness polyneuropathy", "Polyneuropathy, Critical Illness", "Critical Illness Polyneuropathies", "Polyneuropathies, Critical Illness", "polyneuropathy due to critical illness", "Critical illness-associated polyneuropathy", "Critical illness polyneuropathy (disorder)", "polyneuropathy due to critical illness (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "critical illness polyneuropathy", "shortest_name_length": 31}
{"curie": "MONDO:0008435", "names": ["Somatomedin, embryonic", "SOMATOMEDIN, EMBRYONIC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Somatomedin, embryonic", "shortest_name_length": 22}
{"curie": "UMLS:C5420075", "names": ["Sinonasal Chondromesenchymal Hamartoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Chondromesenchymal Hamartoma", "shortest_name_length": 38}
{"curie": "UMLS:C0151559", "names": ["CNS depression", "CNS DEPRESSION", "cns depression", "cns depressions", "CNS depression NOS", "CNS DEPRESSION NOS", "central depression nervous system", "Depression central nervous system", "DEPRESSION CENTRAL NERVOUS SYSTEM", "Central nervous system depression", "Central nervous system depression NOS", "Central nervous system depression (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central nervous system depression (disorder)", "shortest_name_length": 14}
{"curie": "MONDO:0003384", "names": ["Broad Ligament Clear Cell Adenocarcinoma", "uterine ligament clear cell adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine ligament clear cell adenocarcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0032931", "names": ["PHRINL", "Phrinl Syndrome", "PHRINL SYNDROME", "fatal pontocerebellar hypoplasia-hypotonia-respiratory distress syndrome", "Chromosome 1P36.33 Deletion Syndrome, Atad3 Gene Cluster, Autosomal Recessive", "fatal pontocerebellar hypoplasia-hypotonia-respiratory insufficiency syndrome", "CHROMOSOME 1p36.33 DELETION SYNDROME, ATAD3 GENE CLUSTER, AUTOSOMAL RECESSIVE", "PONTOCEREBELLAR HYPOPLASIA, HYPOTONIA, AND RESPIRATORY INSUFFICIENCY SYNDROME, NEONATAL LETHAL", "pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal", "shortest_name_length": 6}
{"curie": "MONDO:0005656", "names": ["Ascaridida infection", "Ascaridida Infections", "infection, Ascaridida", "infections, Ascaridida", "Ascaridida infectious disease", "Ascaridida disease or disorder", "Ascaridida caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ascaridida infectious disease", "shortest_name_length": 20}
{"curie": "UMLS:C1335914", "names": ["G2 Grade 2", "Sarcoma FNCLCC Grade 2", "FNCLCC Sarcoma Grade 2", "Sarcoma Differentiation Score 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FNCLCC Sarcoma Grade 2", "shortest_name_length": 10}
{"curie": "MONDO:0011796", "names": ["Epps", "EPPS", "PEPS", "EPILEPSY, PARTIAL, WITH PERICENTRAL SPIKES", "Epilepsy, Partial, with Pericentral Spikes", "epilepsy, partial, with pericentral spikes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, partial, with pericentral spikes", "shortest_name_length": 4}
{"curie": "MONDO:0032875", "names": ["SSMGA", "SHORT STATURE AND MICROCEPHALY WITH GENITAL ANOMALIES", "short stature and microcephaly with genital anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short stature and microcephaly with genital anomalies", "shortest_name_length": 5}
{"curie": "MONDO:0023249", "names": ["Polyarticular juvenile rheumatoid arthritis", "polyarticular juvenile rheumatoid arthritis", "Polyarticular juvenile rheumatoid arthritis, NOS", "Juvenile polyarthritis rheumatoid factor positive", "Juvenile polyarthritis rheumatoid factor negative"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyarticular juvenile rheumatoid arthritis", "shortest_name_length": 43}
{"curie": "MONDO:0044033", "names": ["PRES", "RPLE", "Posterior leucoencephalopathy syndrome", "posterior leukoencephalopathy syndrome", "Posterior Leukoencephalopathy Syndrome", "syndrome, Posterior leukoencephalopathy", "Leukoencephalopathy Syndrome, Posterior", "leukoencephalopathy syndrome, Posterior", "Syndrome, Posterior Leukoencephalopathy", "Syndromes, Posterior Leukoencephalopathy", "leukoencephalopathy syndromes, Posterior", "Leukoencephalopathy Syndromes, Posterior", "syndromes, Posterior leukoencephalopathy", "Reversible Posterior Cerebral Edema Syndrome", "Posterior Reversible Encephalopathy Syndrome", "Reversible Occipital Parietal Encephalopathy", "reversible occipital parietal encephalopathy", "reversible Posterior cerebral edema syndrome", "Posterior reversible encephalopathy syndrome", "posterior reversible encephalopathy syndrome", "reversible Posterior leukoencephalopathy syndrome", "Reversible Posterior Leukoencephalopathy Syndrome", "Reversible posterior leucoencephalopathy syndrome", "reversible posterior leukoencephalopathy syndrome", "Reversible posterior leukoencephalopathy syndrome", "Posterior reversible encephalopathy syndrome (disorder)", "posterior reversible encephalopathy syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "posterior leukoencephalopathy syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0008700", "names": ["ACHP", "ACHEIROPODY", "Acheiropody", "acheiropody", "acheiropodia", "ACHEIROPODIA", "Acheiropodia", "horn-Kolb syndrome", "Horn-Kolb Syndrome", "Acheiropodia (disorder)", "Agenesis of hands AND feet", "Agenesis of hands and feet", "Brazilian type acheiropody", "Acheiropody, Brazilian type", "ACHEIROPODY, BRAZILIAN TYPE", "acheiropody, Brazilian type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acheiropody", "shortest_name_length": 4}
{"curie": "MONDO:0005878", "names": ["River blindness", "river blindness", "River Blindness", "Blindness, River", "Ocular onchocerciasis", "ocular onchocerciasis", "Ocular Onchocerciasis", "Ocular Onchocerciases", "Onchocerciasis, Ocular", "Onchocerciases, Ocular", "river blindness (etiology)", "river blindness (manifestation)", "Ocular onchocerciasis (disorder)", "eyeball of camera-type eye onchocerciasis", "onchocerciasis of eyeball of camera-type eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ocular onchocerciasis", "shortest_name_length": 15}
{"curie": "UMLS:C3830391", "names": ["Drug Induced Cutaneous Lupus Erythematosus", "Drug-induced cutaneous lupus erythematosus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drug-induced cutaneous lupus erythematosus", "shortest_name_length": 42}
{"curie": "MONDO:0004672", "names": ["Fasciolopsiases", "Fasciolopsiasis", "fasciolopsiasis", "Fasciolopsiosis", "FASCIOLOPSIASIS", "Intestinal distomiasis", "Fasciolopsis; infestation", "Infection by Fasciolopsis", "infestation; Fasciolopsis", "intestinal; fluke disease", "fasciolopsiasis (diagnosis)", "Fasciolopsis buski infection", "fluke; infestation, intestinal", "infestation; fluke, intestinal", "infection by Fasciolopsis buski", "Infection by Fasciolopsis buski", "Giant intestinal fluke infection", "infectious disease by Fasciolopsis", "Infectious Disease by Fasciolopsis", "Infection caused by Fasciolopsis buski", "Infection caused by Fasciolopsis buski (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fasciolopsiasis", "shortest_name_length": 15}
{"curie": "MONDO:0019960", "names": ["Vipoma", "VIPoma", "vipoma", "VIPOMA", "vipomas", "Vipomas", "Vipoma, NOS", "WDHA syndrome", "Vipoma, malignant", "pancreatic vipoma", "VIPoma, malignant", "VIP-producing NET", "VIP-Producing NET", "Pancreatic VIPoma", "Pancreatic cholera", "VIPoma, Pancreatic", "pancreatic cholera", "Pancreatic VIPomas", "VIPomas, Pancreatic", "VIP-secreting tumor", "Diarrheogenic Tumor", "Tumor, Diarrheogenic", "VIP- Secreting tumor", "VIP- secreting tumor", "VIP- Secreting Tumor", "Diarrheogenic Tumors", "Tumors, Diarrheogenic", "VIP Producing Neoplasm", "VIP producing neoplasm", "VIP- secreting neoplasm", "VIP- Secreting Neoplasm", "Verner-Morrison syndrome", "VIP Secreting Tumor (VIPoma)", "VIP-Secreting Tumor (VIPoma)", "VIP-Secreting Tumors (VIPoma)", "Tumor, VIP-Secreting (VIPoma)", "Diarrheogenic Islet Cell Tumor", "Diarrheogenic islet cell tumor", "Tumors, VIP-Secreting (VIPoma)", "Vipoma (morphologic abnormality)", "VIP-producing neuroendocrine tumor", "VIP-Producing Neuroendocrine Tumor", "vasoactive intestinal peptide (VIP) tumor", "Vasoactive Intestinal Peptide (VIP) Tumor", "Vasoactive intestinal peptide-secreting tumor", "vasoactive intestinal peptide-secreting tumor", "vasoactive intestinal peptide producing tumor", "vasoactive intestinal peptide-producing tumor", "Vasoactive Intestinal Peptide Producing Tumor", "Vasoactive Intestinal Peptide-Producing Tumor", "Vasoactive intestinal peptide-secreting tumour", "Vasoactive Intestinal Peptide Secreting Neoplasm", "vasoactive intestinal peptide secreting neoplasm", "Vasoactive Intestinal Peptide Producing Neoplasm", "vasoactive intestinal peptide producing neoplasm", "Watery diarrhea-hypokalemia-achlorhydria syndrome", "watery diarrhea-hypokalemia-achlorhydria syndrome", "watery diarrhea, hypokalemia, and achlorhydria syndrome", "VIP-oma - Vasoactive intestinal peptide-secreting tumor", "malignant vasoactive intestinal peptide-secreting tumor", "VIP-oma - Vasoactive intestinal peptide-secreting tumour", "Vasoactive intestinal peptide-secreting tumor (disorder)", "vasoactive intestinal peptide-secreting tumor (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "VIPoma", "shortest_name_length": 6}
{"curie": "UMLS:C5447974", "names": ["Advanced Salivary Gland Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Salivary Gland Carcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C4744463", "names": ["Recurrent Digestive System Neuroendocrine Carcinoma", "Recurrent Gastrointestinal System Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Digestive System Neuroendocrine Carcinoma", "shortest_name_length": 51}
{"curie": "UMLS:C1336369", "names": ["Stage IVB Liver Cell Carcinoma", "Stage IVB Hepatocellular Cancer", "Stage IVB Hepatocellular Carcinoma", "Stage IVB Carcinoma of Liver Cells", "Stage IVB Carcinoma of the Liver Cells", "Stage IVB Hepatocellular Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Hepatocellular Carcinoma AJCC v7", "shortest_name_length": 30}
{"curie": "UMLS:C0281774", "names": ["Acute Psychosis", "PSYCHOSIS ACUTE", "Acute psychosis", "acute psychosis", "psychosis; acute", "acute; psychosis", "acute; psychotic disorder", "disorder; acute psychotic", "disorder; psychotic, acute", "Acute psychosis (disorder)", "psychotic; disorder, acute", "acute psychosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute psychosis", "shortest_name_length": 15}
{"curie": "UMLS:C2937319", "names": ["internal injury", "Internal injury", "injury; internal", "internal; injury", "internal injuries", "injuries internal", "Internal injury NOS", "Internal injury, NOS", "injuries internal organ"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Internal injury", "shortest_name_length": 15}
{"curie": "MONDO:0022798", "names": ["Cohen lockood wyborney syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cohen lockood wyborney syndrome", "shortest_name_length": 31}
{"curie": "MONDO:0002021", "names": ["Gum disease", "Gum Disease", "gum disease", "gum disorder", "Disease;gums", "Gum disorder", "Gums--Diseases", "gingiva disease", "GINGIVAL DISEASE", "gingival disease", "Gingival disease", "Gingival Disease", "gingiva disorder", "Gum disease, NOS", "Gingival Disorder", "Gingival Diseases", "Gingival disorder", "gingival disorder", "gingival diseases", "Disease, Gingival", "disease of gingiva", "Diseases, Gingival", "disorder of gingiva", "Gingival disease, NOS", "Gingival disorder NOS", "Gingival disorder, NOS", "disease (or disorder); gum", "gingiva disease or disorder", "Gingival disease (disorder)", "disease or disorder of gingiva", "disease (or disorder); gingiva"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gingival disorder", "shortest_name_length": 11}
{"curie": "MONDO:0013670", "names": ["MCVD", "myopia, high, with cataract and vitreoretinal degeneration", "MYOPIA, HIGH, WITH CATARACT AND VITREORETINAL DEGENERATION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopia, high, with cataract and vitreoretinal degeneration", "shortest_name_length": 4}
{"curie": "MONDO:0014362", "names": ["CHROMOSOME 16 INVERSION, 0.45-MB", "chromosome 16 inversion, 0.45-Mb"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 16 inversion, 0.45-Mb", "shortest_name_length": 32}
{"curie": "MONDO:0000919", "names": ["ampulla of vater cancer", "ampulla of Vater cancer", "hepatopancreatic ampulla cancer", "Malignant Ampulla of Vater Tumor", "malignant ampulla of Vater tumor", "cancer of hepatopancreatic ampulla", "malignant tumor of ampulla of Vater", "malignant ampulla of Vater neoplasm", "Malignant Ampulla of Vater Neoplasm", "Malignant tumor of ampulla of Vater", "Malignant Tumor of Ampulla of Vater", "Malignant tumour of ampulla of Vater", "malignant tumour of ampulla of vater", "Malignant neoplasm of ampulla of vater", "Malignant Neoplasm of Ampulla of Vater", "Malignant neoplasm of ampulla of Vater", "malignant neoplasm of ampulla of Vater", "Malignant Tumor of the Ampulla of Vater", "malignant tumor of the ampulla of Vater", "Malignant Neoplasm of the Ampulla of Vater", "malignant neoplasm of the ampulla of Vater", "malignant hepatopancreatic ampulla neoplasm", "malignant neoplasm of hepatopancreatic ampulla", "Malignant tumor of ampulla of Vater (disorder)", "malignant neoplasm of ampulla of Vater (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ampulla of vater cancer", "shortest_name_length": 23}
{"curie": "MONDO:0021204", "names": ["OTITIS MEDIA CHRONIC", "Otitis media chronic", "chronic otitis media", "otitis media chronic", "Otitis media;chronic", "CHRONIC OTITIS MEDIA", "Chronic otitis media", "chronic media otitis", "EAR INFECTION CHRONIC", "chronic ear infection", "Otitis media, chronic", "ear infection chronic", "Chronic ear infection", "chronic ear infections", "otitis; media, chronic", "chronic otitis media nos", "Otitis media chronic NOS", "Chronic otitis media NOS", "Chronic otitis media, NOS", "Chronic middle ear infection", "chronic otitis media (disease)", "Chronic otitis media (disorder)", "otitis media (disease), chronic", "chronic otitis media (diagnosis)", "Chronic infections of the middle ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic otitis media", "shortest_name_length": 20}
{"curie": "UMLS:C0349470", "names": ["Amniotic fluid aspiration", "aspiration; amniotic fluid", "amniotic fluid; aspiration", "Neonatal aspiration of liquor", "Aspiration of liquor in newborn", "Neonatal aspiration of amniotic fluid", "Neonatal Aspiration of Amniotic Fluid", "Aspiration of amniotic fluid in newborn", "Neonatal aspiration of amniotic fluid (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neonatal aspiration of amniotic fluid", "shortest_name_length": 25}
{"curie": "UMLS:C0277577", "names": ["Psychic disease", "PSYCHIC DISORDER", "PSYCHIC DISTURBANCE", "Psychic disturbance", "Psychic disease, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Psychic disease", "shortest_name_length": 15}
{"curie": "UMLS:C4329661", "names": ["T Acute Lymphoblastic Leukemia in Remission", "Childhood T Acute Lymphoblastic Leukemia in Remission"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood T Acute Lymphoblastic Leukemia in Remission", "shortest_name_length": 43}
{"curie": "UMLS:C2828202", "names": ["Stage IIA Bone Cancer", "Stage IIA Bone Cancer AJCC v7", "Stage IIA Bone Cancer  AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Bone Cancer AJCC v7", "shortest_name_length": 21}
{"curie": "UMLS:C5420329", "names": ["Intercalated Duct Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intercalated Duct Hyperplasia", "shortest_name_length": 29}
{"curie": "MONDO:0013150", "names": ["IPD", "PKDYS", "infantile Parkinsonism-dystonia", "Parkinsonism-dystonia infantile", "parkinsonism-dystonia, infantile", "Parkinsonism-Dystonia, Infantile", "PARKINSONISM-dystonia, infantile", "dopamine transporter deficiency syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parkinsonism-dystonia, infantile", "shortest_name_length": 3}
{"curie": "MONDO:0030054", "names": ["DEE86", "EIEE86", "early infantile epileptic encephalopathy 86", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 86", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 86", "epileptic encephalopathy, early infantile, 86", "developmental and epileptic encephalopathy 86", "developmental and epileptic encephalopathy, 86"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 86", "shortest_name_length": 5}
{"curie": "UMLS:C3640070", "names": ["Spinal Cord Infarct During Birth", "Spinal Cord Infarct during Birth", "Spinal Cord Infarct Related to Birth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spinal Cord Infarct During Birth", "shortest_name_length": 32}
{"curie": "UMLS:C0015378", "names": ["Contrast Media Extravasation", "Contrast media extravasation", "Extravasation of Contrast Media", "Extravasation of contrast medium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extravasation of Contrast Media", "shortest_name_length": 28}
{"curie": "UMLS:C1511257", "names": ["Borderline Fallopian Tube Serous Tumor", "Borderline Fallopian Tube Serous Neoplasm", "Borderline Fallopian Tube Serous Tumor/Atypical Proliferative Serous Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Fallopian Tube Serous Tumor", "shortest_name_length": 38}
{"curie": "MONDO:0018702", "names": ["TAFRO syndrome", "Castleman-Kojima disease", "thrombocytopenia-anasarca-fever-renal insufficiency-organomegaly syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Castleman-Kojima disease", "shortest_name_length": 14}
{"curie": "MONDO:0013289", "names": ["AGM4", "agammaglobulinemia 4", "BLNK autosomal agammaglobulinemia", "AGAMMAGLOBULINEMIA 4, AUTOSOMAL RECESSIVE", "agammaglobulinemia 4, autosomal recessive", "autosomal agammaglobulinemia caused by mutation in BLNK", "agammaglobulinemia, autosomal recessive, due to Blnk defect", "AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO BLNK DEFECT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "agammaglobulinemia 4, autosomal recessive", "shortest_name_length": 4}
{"curie": "UMLS:C0280311", "names": ["Mouth Adenoid Cystic Carcinoma", "Oral Cavity Adenoid Cystic Cancer", "Adenoid Cystic Carcinoma of Mouth", "oral cavity adenoid cystic carcinoma", "Oral Cavity Adenoid Cystic Carcinoma", "adenoid cystic carcinoma, oral cavity", "Adenoid Cystic Carcinoma of the Mouth", "adenoid cystic carcinoma of oral cavity", "Adenoid Cystic Carcinoma of Oral Cavity", "Adenoid Cystic Carcinoma of the Oral Cavity", "Adenoid cystic carcinoma of the oral cavity", "adenoid cystic carcinoma of oral cavity (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenoid cystic carcinoma of the oral cavity", "shortest_name_length": 30}
{"curie": "MONDO:0013631", "names": ["LNCR5", "lung cancer susceptibility 5", "LUNG CANCER SUSCEPTIBILITY 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung cancer susceptibility 5", "shortest_name_length": 5}
{"curie": "UMLS:C1332482", "names": ["Benign Childhood Brain Tumor", "Benign Pediatric Brain Tumor", "Benign Childhood Tumor of Brain", "Benign Pediatric Tumor of Brain", "Benign Childhood Brain Neoplasm", "Benign Pediatric Brain Neoplasm", "Childhood Benign Brain Neoplasms", "Benign Childhood Neoplasm of Brain", "Benign Pediatric Neoplasm of Brain", "Benign Childhood Tumor of the Brain", "Benign Pediatric Tumor of the Brain", "Benign Childhood Neoplasm of the Brain", "Benign Pediatric Neoplasm of the Brain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Childhood Brain Neoplasm", "shortest_name_length": 28}
{"curie": "MONDO:0014636", "names": ["COXPD25", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 25", "combined oxidative phosphorylation deficiency 25", "Combined oxidative phosphorylation defect type 25", "combined oxidative phosphorylation defect type 25", "MARS2 combined oxidative phosphorylation deficiency", "combined oxidative phosphorylation deficiency type 25", "COXPD25 - combined oxidative phosphorylation defect type 25", "Combined oxidative phosphorylation defect type 25 (disorder)", "combined oxidative phosphorylation deficiency caused by mutation in MARS2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation defect type 25", "shortest_name_length": 7}
{"curie": "MONDO:0012011", "names": ["ADCAD1", "CAD autosomal dominant 1", "MEF2A coronary artery disease", "CAD autosomal dominant 1 (diagnosis)", "coronary artery disease autosomal dominant 1", "CORONARY ARTERY DISEASE/MYOCARDIAL INFARCTION", "CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT 1", "coronary artery disease, autosomal dominant, 1", "CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1", "Coronary Artery Disease, Autosomal Dominant, 1", "CORONARY ARTERY DISEASE WITH MYOCARDIAL INFARCTION", "coronary artery disease with myocardial infarction", "Coronary Artery Disease With Myocardial Infarction", "coronary artery disease caused by mutation in MEF2A", "coronary artery disease, autosomal dominant, type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coronary artery disease, autosomal dominant, 1", "shortest_name_length": 6}
{"curie": "MONDO:0043197", "names": ["ruvalcaba churesigaew myhre syndrome", "Ruvalcaba Churesigaew Myhre syndrome", "onset of senility in the early teens, atrophic skin, hypogonadism, retinal and vascular sclerosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ruvalcaba churesigaew myhre syndrome", "shortest_name_length": 36}
{"curie": "UMLS:C5556719", "names": ["Recurrent Bronchogenic Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Bronchogenic Carcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C0278823", "names": ["Bladder cancer stage II", "Stage II Bladder Cancer", "stage II bladder cancer", "bladder cancer, stage II", "bladder cancer, stage B1", "Stage II Bladder Carcinoma", "Carcinoma bladder stage II", "Cancer of Bladder Stage II", "Bladder carcinoma stage II", "Stage II Carcinoma of Bladder", "stage II cancer of the bladder", "Cancer of the Bladder Stage II", "stage B1 cancer of the bladder", "Stage II Bladder Cancer AJCC v6", "cancer of the bladder, stage B1", "cancer of the bladder, stage II", "Stage II Bladder Cancer AJCC v7", "stage II carcinoma of the bladder", "stage B1 carcinoma of the bladder", "Stage II Carcinoma of the Bladder", "Stage II Bladder Carcinoma AJCC v7", "Urinary bladder carcinoma stage II", "Carcinoma urinary bladder stage II", "carcinoma of the bladder, stage B1", "Stage II Bladder Carcinoma AJCC v6", "carcinoma of the bladder, stage II", "Stage II Urinary Bladder Carcinoma", "Stage II Carcinoma of Urinary Bladder", "Jewett-Marshall Stage B Bladder Cancer", "Stage II Bladder Cancer AJCC v6 and v7", "Stage II Carcinoma of the Urinary Bladder", "Jewett-Marshall Stage B Bladder Carcinoma", "Jewett-Marshall Stage B Urinary Bladder Cancer", "Jewett-Marshall Stage B Urinary Bladder Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Bladder Cancer AJCC v6 and v7", "shortest_name_length": 23}
{"curie": "MONDO:0000755", "names": ["Eccyesis", "eccyesis", "PREGNANCY ECTOPIC", "Pregnancy;ectopic", "Ectopic pregnancy", "ectopic pregnancy", "Ectopic Pregnancy", "Pregnancy ectopic", "ECTOPIC PREGNANCY", "Pregnancy, ectopic", "pregnancy, ectopic", "Pregnancy, Ectopic", "Ectopic Pregnancies", "ECTOPIC PREGNANCIES", "ectopic pregnancies", "Pregnancies, Ectopic", "Ectopic pregnancy NOS", "EP - Ectopic pregnancy", "Extrauterine pregnancy", "Ectopic pregnancy, NOS", "EXTRAUTERINE PREGNANCY", "extrauterine pregnancy", "Extrauterine Pregnancy", "extrauterine; pregnancy", "Extra-uterine pregnancy", "Pregnancy, Extrauterine", "pregnancy; extrauterine", "Extrauterine Pregnancies", "Pregnancies, Extrauterine", "Ectopic pregnancy (disorder)", "ectopic pregnancy (diagnosis)", "Unspecified ectopic pregnancy", "Ectopic pregnancy, unspecified", "extrauterine gestation or pregnancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectopic pregnancy", "shortest_name_length": 8}
{"curie": "UMLS:C0855123", "names": ["Stage IV Follicular Lymphoma", "Follicular lymphoma stage IV", "Ann Arbor Stage IV Follicular Lymphoma", "Follicle center lymphoma, follicular grade I, II, III stage IV", "Follicle Centre Lymphoma, Follicular Grade I, II, III Stage IV", "Follicle centre lymphoma, follicular grade I, II, III stage IV"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Follicle center lymphoma, follicular grade I, II, III stage IV", "shortest_name_length": 28}
{"curie": "MONDO:0006731", "names": ["Drug-Induced Acathisia", "Drug induced akathisia", "Drug Induced Akathisia", "Drug induced acathisia", "drug-induced akathisia", "Drug-induced akathisia", "Drug-Induced Akathisia", "Akathisia, Drug-Induced", "Akathisia, Drug Induced", "Acathisia, Drug Induced", "Acathisia, Drug-Induced", "Akathisia caused by drug", "drug-induced akathisia (diagnosis)", "Akathisia caused by drug (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "drug-induced akathisia", "shortest_name_length": 22}
{"curie": "MONDO:0013962", "names": ["SPG53", "hereditary spastic paraplegia 53", "hereditary spastic paraplegia type 53", "autosomal recessive spastic paraplegia 53", "spastic paraplegia 53, autosomal recessive", "SPASTIC PARAPLEGIA 53, AUTOSOMAL RECESSIVE", "autosomal recessive spastic paraplegia type 53", "Autosomal recessive spastic paraplegia type 53", "VPS37A autosomal recessive complex spastic paraplegia", "familial spastic paraplegia autosomal recessive type 53", "Autosomal recessive spastic paraplegia type 53 (disorder)", "Autosomal recessive spastic paraplegia type 53 (diagnosis)", "autosomal recessive complex spastic paraplegia caused by mutation in VPS37A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 53", "shortest_name_length": 5}
{"curie": "MONDO:0010714", "names": ["PMD", "HLD1", "extracortical axial aplasia", "sudanophilic leukodystrophy", "Sudanophilic leukodystrophy", "leukodystrophy, sudanophilic", "Pelizaeus-Merzbacher disease", "Pelizaeus Merzbacher disease", "Pelizaeus-Merzbacher Disease", "pelizaeus-merzbacher disease", "extracortical axial; aplasia", "pelizaeus merzbacher disease", "PELIZAEUS-MERZBACHER DISEASE", "Pelizaeus Merzbacher Disease", "aplasia; extracortical axial", "Leukodystrophy, sudanophilic", "Pelizaeus-Merzbacher syndrome", "familial centrolobal sclerosis", "diffuse familial brain sclerosis", "hypomyelinating leukodystrophy 1", "Diffuse familial brain sclerosis", "Leukodystrophy, Hypomyelinating, 1", "LEUKODYSTROPHY, HYPOMYELINATING, 1", "Pelizaeus-Merzbacher disease (PMD)", "leukodystrophy, hypomyelinating, 1", "Pelizaeus-Merzbacher brain sclerosis", "Pelizaeus Merzbacher Brain Sclerosis", "Pelizaeus-Merzbacher Brain Sclerosis", "Brain Pelizaeus-Merzbacher Sclerosis", "Pelizaeus Merzbacher brain sclerosis", "Pelizaeus-Merzbacher Sclerosis, Brain", "Brain Sclerosis, Pelizaeus-Merzbacher", "Pelizaeus Merzbacher Sclerosis, Brain", "brain; sclerosis, Pelizaeus-Merzbacher", "sclerosis; brain, Pelizaeus-Merzbacher", "Pelizaeus-Merzbacher disease (disorder)", "sudanophilic leukodystrophy (diagnosis)", "Pelizaeus Merzbacher disease (diagnosis)", "aplasia axialis extracorticalis congenita", "Pelizaeus-Merzbacher disease, X-linked recessive", "sudanophilic leukodystrophy, Paelizeus-Merzbacher type", "Sudanophilic leukodystrophy, Paelizeus-Merzbacher type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pelizaeus-Merzbacher disease", "shortest_name_length": 3}
{"curie": "MONDO:0014142", "names": ["LGMD2T", "LGMDR19", "MDDGC14", "LGMD type 2T", "LGMD-GMPPB related", "GMPPB-related LGMD R19", "limb-girdle muscular dystrophy type 2T", "muscular dystrophy limb-girdle type 2T", "Limb-girdle muscular dystrophy type 2T", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2T", "muscular dystrophy, limb-girdle, type 2T", "GMPPB-related limb-girdle muscular dystrophy R19", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 19", "GMPPB autosomal recessive limb-girdle muscular dystrophy", "Autosomal recessive limb-girdle muscular dystrophy type 2T", "autosomal recessive limb-girdle muscular dystrophy type 2T", "Autosomal recessive limb girdle muscular dystrophy type 2T", "muscular dystrophy-dystroglycanopathy (limb-girdle) type C14", "muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 14", "muscular dystrophy-dystroglycanopathy limb-girdle GMPPB-related", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, GMPPB-RELATED", "muscular dystrophy-dystroglycanopathy, limb-girdle, GMPPB-related", "Autosomal recessive limb girdle muscular dystrophy type 2T (disorder)", "autosomal recessive limb-girdle muscular dystrophy caused by mutation in GMPPB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive limb-girdle muscular dystrophy type 2T", "shortest_name_length": 6}
{"curie": "UMLS:C4724974", "names": ["Mitochondrially Inherited Nonsyndromic Sensorineural Deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mitochondrially Inherited Nonsyndromic Sensorineural Deafness", "shortest_name_length": 61}
{"curie": "UMLS:C0751708", "names": ["General Peroxisomal Dysfunction", "Peroxisomal Dysfunction, General", "Dysfunction, General Peroxisomal", "General Peroxisomal Dysfunctions", "Peroxisomal Dysfunctions, General", "Dysfunctions, General Peroxisomal", "General loss of peroxisomal function", "General loss of peroxisomal function (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peroxisomal Dysfunction, General", "shortest_name_length": 31}
{"curie": "UMLS:C1562312", "names": ["Estrogen receptor positive tumor", "estrogen receptor positive tumor", "Oestrogen receptor positive tumour", "Estrogen receptor positive tumor (disorder)", "estrogen receptor positive tumor (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Estrogen receptor positive tumor", "shortest_name_length": 32}
{"curie": "UMLS:C0028715", "names": ["metabolic nutritional disorders", "disorders metabolic nutritional", "NUTRITIONAL AND METABOLIC DISEASES", "nutritional and metabolic diseases", "Nutritional and Metabolic Diseases", "Metabolic and Nutritional Disorders", "METABOLIC AND NUTRITIONAL DISORDERS", "Metabolic and Nutritional Diseases and Syndromes", "NUTRITIONAL AND METABOLIC DISEASES: GENERAL TERMS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nutritional and Metabolic Diseases", "shortest_name_length": 31}
{"curie": "MONDO:0032730", "names": ["HLD18", "hypomyelinating leukodystrophy 18", "leukodystrophy, hypomyelinating, 18", "LEUKODYSTROPHY, HYPOMYELINATING, 18"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukodystrophy, hypomyelinating, 18", "shortest_name_length": 5}
{"curie": "MONDO:0005950", "names": ["Salmonellosis", "salmonellosis", "salmonella poison", "poisoning salmonella", "Enteritis;salmonella", "Enteric paratyphosis", "ENTERITIS SALMONELLA", "salmonella enteritis", "Salmonella poisoning", "salmonella poisoning", "Salmonella enteritis", "Salmonella; poisoning", "poisoning; Salmonella", "Salmonella Food Poisoning", "Poisoning;food;salmonella", "Salmonella food poisoning", "salmonella food poisoning", "Salmonella gastroenteritis", "Food Poisoning, Salmonella", "GASTROENTERITIS SALMONELLA", "Salmonella Food Poisonings", "FOOD POISONING, SALMONELLA", "salmonella gastroenteritis", "Poisoning, Salmonella Food", "Gastroenteritis salmonella", "Food Poisonings, Salmonella", "gastroenteritis; Salmonella", "Poisonings, Salmonella Food", "Salmonella; gastroenteritis", "Salmonella enteritis (diagnosis)", "Salmonella caused gastroenteritis", "food; poisoning, due to salmonella", "poisoning; food, due to salmonella", "Salmonella food poisoning (disorder)", "Salmonella gastroenteritis (disorder)", "Salmonella gastroenteritis (diagnosis)", "GASTROENTERITIS, SALMONELLA, NONTYPHOID", "Salmonella; infection, with (gastro)enteritis", "infection; Salmonella, with (gastro)enteritis", "food; poisoning, due to salmonella, with gastroenteritis", "poisoning; food, due to salmonella, with gastroenteritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Salmonella gastroenteritis", "shortest_name_length": 13}
{"curie": "MONDO:0004175", "names": ["Mucin-Rich Endometrial Endometrioid Adenocarcinoma", "mucin-rich endometrial endometrioid adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucin-rich endometrial endometrioid adenocarcinoma", "shortest_name_length": 50}
{"curie": "MONDO:0041284", "names": ["JACKSONIAN EPILEPSY", "epilepsy jacksonian", "Jacksonian epilepsy", "jacksonian epilepsy", "EPILEPSY, JACKSONIAN", "epilepsy; jacksonian", "Motor cortex epilepsy", "motor cortex epilepsy", "Epilepsy, Jacksonian NOS", "primary motor cortex epilepsy", "epilepsy of primary motor cortex", "Motor cortex epilepsy (disorder)", "Motor cortex epilepsy (diagnosis)", "frontal lobe epilepsy motor cortex"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary motor cortex epilepsy", "shortest_name_length": 19}
{"curie": "MONDO:0008869", "names": ["SCKL", "Sckl", "SCKL1", "Seckel syndrome 1", "SECKEL SYNDROME 1", "Seckel syndrome 3", "SECKEL SYNDROME 3", "Seckel Syndrome 3", "ATR Seckel syndrome", "BIRD-HEADED DWARFISM", "SECKEL-TYPE DWARFISM", "Bird-headed dwarfism", "Seckel-type dwarfism", "NANOCEPHALIC DWARFISM", "nanocephalic dwarfism", "Nanocephalic dwarfism", "Seckel syndrome type 1", "microcephalic primordial dwarfism 1", "Microcephalic primordial dwarfism 1", "Microcephalic Primordial Dwarfism I", "MICROCEPHALIC PRIMORDIAL DWARFISM I", "microcephalic primordial dwarfism I", "Seckel syndrome caused by mutation in ATR"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Seckel syndrome 1", "shortest_name_length": 4}
{"curie": "MONDO:0012932", "names": ["MYP16", "myopia 16", "Myopia 16", "MYOPIA 16 (disorder)", "myopia 16, autosomal dominant", "MYOPIA 16, AUTOSOMAL DOMINANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopia 16, autosomal dominant", "shortest_name_length": 5}
{"curie": "MONDO:0005831", "names": ["scrofula", "king evil", "Kings Evil", "king's evil", "Evil, Kings", "King's Evil", "Kings Evils", "Evils, Kings", "Evil, King's", "Tuberculous adenitis", "tuberculous adenitis", "adenitis; tuberculous", "tuberculosis; adenitis", "Lymph Node Tuberculoses", "Lymph node tuberculosis", "lymph node; tuberculous", "lymph node tuberculosis", "Lymph Node Tuberculosis", "Tuberculoses, Lymph Node", "Tuberculosis, Lymph Node", "lymph nodes tuberculosis", "tuberculosis; lymph node", "LYMPH NODES, TUBERCULOSIS", "Tuberculous Lymphadenitis", "Tuberculous adenitis, NOS", "tuberculous lymphadenitis", "TUBERCULOUS LYMPHADENITIS", "TUBERCULOSIS LYMPHADENITIS", "lymphadenitis; tuberculous", "Lymphadenitis, Tuberculous", "tuberculosis lymphadenitis", "Tuberculosis of lymph node", "tuberculous lymphadenopathy", "tuberculosis; lymphadenitis", "Lymph node tuberculosis NOS", "Tuberculous lymphadenopathy", "lymphadenopathy; tuberculous", "tuberculosis; lymphadenopathy", "Tuberculous adenitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymph node tuberculosis", "shortest_name_length": 8}
{"curie": "MONDO:0045018", "names": ["creatine synthesis disease", "disorder of creatine synthesis", "Disorder of creatine synthesis", "creatine biosynthetic process disease", "Disorder of creatine synthesis (disorder)", "disorder of creatine biosynthetic process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "creatine biosynthetic process disease", "shortest_name_length": 26}
{"curie": "MONDO:0002933", "names": ["Osteosclerosis", "osteosclerosis", "OSTEOSCLEROSIS", "Osteoscleroses", "Osteosclerosis NOS", "Bone density increased", "Increased bone density", "Osteosclerosis of bones", "Osteosclerosis (disorder)", "Increased bone mineral density"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteosclerosis", "shortest_name_length": 14}
{"curie": "MONDO:0006537", "names": ["pigmentation; conjunctiva", "Conjunctival pigmentation", "conjunctival pigmentation", "conjunctiva; pigmentation", "Conjunctival pigmentations", "conjunctival pigmentations", "Conjunctival pigmentation, NOS", "Conjunctival pigmentation (disorder)", "conjunctival pigmentations (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "conjunctival pigmentation", "shortest_name_length": 25}
{"curie": "UMLS:C0349637", "names": ["c-ALL", "Common ALL", "Common precursor B ALL", "Common acute lymphoblastic leukemia", "Common Acute Lymphoblastic Leukemia", "Common acute lymphoblastic leukaemia", "CALL - Common acute lymphoblastic leukemia", "CALL - Common acute lymphoblastic leukaemia", "Common acute lymphoblastic leukemia (disorder)", "Common acute lymphoblastic leukemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Common Acute Lymphoblastic Leukemia", "shortest_name_length": 5}
{"curie": "MONDO:0018043", "names": ["Thomas syndrome", "Potter sequence-cleft lip/palate-cardiopathy syndrome", "Potter sequence cleft lip and palate cardiopathy syndrome", "Potter sequence cleft lip and palate cardiopathy syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thomas syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0012740", "names": ["Distal del(22)(q11.2)", "distal del(22)(q11.2)", "Distal monosomy 22q11.2", "distal monosomy 22q11.2", "22q11.2 deletion syndrome", "distal 22q11.2 microdeletion syndrome", "Distal 22q11.2 microdeletion syndrome", "DISTAL CHROMOSOME 22q11.2 DELETION SYNDROME", "Distal Chromosome 22q11.2 Deletion Syndrome", "distal chromosome 22Q11.2 deletion syndrome", "chromosome 22q11.2 deletion syndrome, distal", "CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL", "Chromosome 22q11.2 Deletion Syndrome, Distal", "Distal 22q11.2 microdeletion syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 22q11.2 deletion syndrome, distal", "shortest_name_length": 21}
{"curie": "UMLS:C1719906", "names": ["Meningitis due to Klebsiella mobilis", "Meningitis caused by Klebsiella mobilis", "Meningitis caused by Klebsiella aerogenes", "Meningitis caused by Aerobacter aerogenes", "Meningitis caused by Enterobacter aerogenes", "Meningitis caused by Klebsiella aerogenes (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meningitis caused by Klebsiella aerogenes", "shortest_name_length": 36}
{"curie": "MONDO:0016151", "names": ["qualitative or quantitative defects of perlecan"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of perlecan", "shortest_name_length": 47}
{"curie": "UMLS:C1332260", "names": ["ACIN", "ASIN", "Anal Canal Dysplasia", "Anal Canal Squamous Dysplasia", "Anal Canal Intraepithelial Neoplasia", "Anal Squamous Intraepithelial Neoplasia", "Anal Canal Squamous Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anal Canal Intraepithelial Neoplasia", "shortest_name_length": 4}
{"curie": "UMLS:C0334566", "names": ["Odontogenic Ghost Cell Neoplasm", "odontogenic ghost cell carcinoma", "Ghost cell odontogenic carcinoma", "Odontogenic ghost cell carcinoma", "Ghost Cell Odontogenic Carcinoma", "Odontogenic ghost cell carcinoma (disorder)", "odontogenic ghost cell carcinoma (diagnosis)", "Odontogenic ghost cell carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ghost Cell Odontogenic Carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0018044", "names": ["Primary hypersomnia", "Primary Hypersomnia", "primary hypersomnia", "primary; hypersomnia", "hypersomnia; primary", "idiopathic hypersomnia", "Idiopathic hypersomnia", "Idiopathic Hypersomnia", "Hypersomnia, Idiopathic", "Idiopathic Hypersomnias", "Hypersomnias, Idiopathic", "Idiopathic hypersomnia NOS", "idiopathic hypersomnolence", "Idiopathic Hypersomnolence", "Idiopathic Hypersomnolences", "Hypersomnolence, Idiopathic", "Hypersomnolences, Idiopathic", "Idiopathic CNS Hypersomnolence", "Primary hypersomnia (disorder)", "idiopathic cns hypersomnolence", "Idiopathic CNS Hypersomnolences", "Idiopathic excessive sleepiness", "Hypersomnolence, Idiopathic CNS", "primary hypersomnia (diagnosis)", "CNS Hypersomnolence, Idiopathic", "Hypersomnolence, CNS, Idiopathic", "CNS Hypersomnolences, Idiopathic", "Hypersomnolences, Idiopathic CNS", "Idiopathic hypersomnia (disorder)", "Idiopathic Central Nervous System Hypersomnolence", "Idiopathic central nervous system hypersomnolence"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic hypersomnia", "shortest_name_length": 19}
{"curie": "MONDO:0019351", "names": ["open spine", "cleft spine", "isolated spina bifida", "isolated spina bifida (disease)", "nonsyndromic spina bifida (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated spina bifida", "shortest_name_length": 10}
{"curie": "UMLS:C4527073", "names": ["Pathologic Stage IV Merkel Cell Carcinoma AJCC v8", "Pathologic Stage IV Neuroendocrine Carcinoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IV Merkel Cell Carcinoma AJCC v8", "shortest_name_length": 49}
{"curie": "MONDO:0022936", "names": ["De Hauwere Leroy Adriaenssens syndrome", "de Hauwere Leroy adriaenssens syndrome", "Iris dysplasia, orbital hypertelorism, and psychomotor retardation", "iris dysplasia, orbital hypertelorism, and psychomotor retardation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "de Hauwere Leroy adriaenssens syndrome", "shortest_name_length": 38}
{"curie": "UMLS:C5668241", "names": ["Metastatic Ovarian Mucinous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Ovarian Mucinous Adenocarcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0024637", "names": ["sarcoma", "sarcomas", "Soft tissue cancer", "cancer of the soft tissue", "Neoplasm malig;soft tissue", "SOFT TISSUE TUMOR MALIGNANT", "mesenchymal malignant tumor", "Malignant Soft Tissue Tumor", "malignant soft tissue tumor", "Soft tissue tumor, malignant", "Malignant tumor of soft tissue", "malignant tumor of soft tissue", "malignant soft tissue neoplasm", "Malignant Tumor of Soft Tissue", "Malignant Soft Tissue Neoplasm", "Malignant soft tissue neoplasm", "Malignant tumour of soft tissue", "Malignant neoplasm of soft tissue", "Malignant Neoplasm of Soft Tissue", "malignant neoplasm of soft tissue", "Malignant Tumor of the Soft Tissue", "Malignant soft tissue neoplasm NOS", "malignant tumor of the soft tissue", "Malignant Neoplasm of the Soft Tissue", "malignant neoplasm of the soft tissue", "malignant neosplasm of the soft tissue", "Malignant neoplasm of soft tissue (disorder)", "malignant neoplasm of soft tissue (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant soft tissue neoplasm", "shortest_name_length": 7}
{"curie": "MONDO:0043314", "names": ["M. marinum", "Aquarium granuloma", "aquarium granuloma", "Fish tank granuloma", "fish tank granuloma", "swimming pool granuloma", "Swimming pool granuloma", "swimming-pool granuloma", "granuloma; swimming-pool", "swimming-pool; granuloma", "Fish tank granuloma (disorder)", "mycobacterium marinum infection", "Fish tank granuloma (diagnosis)", "Swimming pool granuloma disease", "Mycobacterium marinum Infection", "Mycobacterium marinum infection", "Mycobacterium marinum skin disease", "Infection with Mycobacterium marinum", "Infection due to Mycobacterium marinum", "infectious disease Mycobacterium marinum", "Mycobacterium marinum caused skin disease", "Infection caused by Mycobacterium marinum", "Infection caused by Mycobacterium marinum (disorder)", "infectious disease Mycobacterium marinum (diagnosis)", "infectious disease Mycobacterium marinum fish tank granuloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aquarium granuloma", "shortest_name_length": 10}
{"curie": "MONDO:0016718", "names": ["CPC", "choroid plexus cancer", "Choroid Plexus Cancer", "choroid plexus carcinoma", "CHOROID PLEXUS CARCINOMA", "Choroid plexus carcinoma", "cancer of choroid plexus", "Choroid Plexus Carcinoma", "Cancer of Choroid Plexus", "carcinoma of choroid plexus", "Carcinoma of Choroid Plexus", "Cancer of the Choroid Plexus", "cancer of the choroid plexus", "Malignant Choroid Plexus Tumor", "carcinoma of the choroid plexus", "Carcinoma of the Choroid Plexus", "Malignant Choroid Plexus Tumors", "Malignant tumor of choroid plexus", "Malignant Choroid Plexus Neoplasm", "Malignant Tumor of Choroid Plexus", "malignant tumor of choroid plexus", "Malignant tumour of choroid plexus", "Malignant Choroid Plexus Neoplasms", "Anaplastic choroid plexus papilloma", "Choroid plexus papilloma, malignant", "Anaplastic Choroid Plexus Papilloma", "anaplastic choroid plexus papilloma", "Choroid plexus carcinoma (disorder)", "Choroid plexus papilloma, anaplastic", "malignant neoplasm of choroid plexus", "papilloma; choroid plexus, malignant", "choroid plexus; papilloma, malignant", "CARCINOMA, CHOROID PLEXUS, MALIGNANT", "anaplastic; papilloma choroid plexus", "Malignant neoplasm of choroid plexus", "carcinoma, choroid plexus, malignant", "Malignant Neoplasm of Choroid Plexus", "choroid plexus; papilloma, anaplastic", "papilloma; choroid plexus, anaplastic", "Malignant Tumor of the Choroid Plexus", "carcinoma of choroid plexus (diagnosis)", "plexus choroideus; papilloma, malignant", "malignant neoplasm of the choroid plexus", "plexus choroideus; papilloma, anaplastic", "Malignant Neoplasm of the Choroid Plexus", "Choroid plexus papilloma, anaplastic type", "Malignant tumor of choroid plexus (disorder)", "malignant neoplasm of choroid plexus (diagnosis)", "Choroid plexus carcinoma (morphologic abnormality)", "choroid plexus carcinoma (morphologic abnormality)", "neoplasm - brain cerebral ventricle malignant choroid plexus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choroid plexus carcinoma", "shortest_name_length": 3}
{"curie": "MONDO:0018381", "names": ["epiphysitis", "apophysitis", "osteochondrosis", "OSTEOCHONDROSIS", "osteochondritis", "osteochondroses", "Osteochondroses", "Osteochondrosis", "Epiphyseal necrosis", "epiphyseal necrosis", "Osteochondrosis NOS", "Osteochondrosis, NOS", "Osteochondropathy-juven", "Juvenile osteochondrosis", "juvenile osteochondrosis", "Juvenile osteochondritis", "Epiphyseal necrosis, NOS", "Juvenile Osteochondrosis", "osteochondritis juvenilis", "osteochondritis; juvenile", "Osteochondrosis juvenilis", "juvenile; osteochondrosis", "juvenile; osteochondritis", "Osteochondritis juvenilis", "osteochondrosis; juvenile", "Epiphyseal ischemic necrosis", "Juvenile osteochondritis NOS", "Juvenile osteochondrosis NOS", "Juvenile osteochondrosis, NOS", "Juvenile osteochondritis, NOS", "Epiphyseal ischaemic necrosis", "Other juvenile osteochondrosis", "Juvenile osteochondrosis syndrome", "Epiphyseal ischemic necrosis, NOS", "Epiphyseal ischaemic necrosis, NOS", "Juvenile osteochondritis (disorder)", "juvenile osteochondrosis (diagnosis)", "Juvenile osteochondrosis, unspecified", "Osteochondrosis specified as juvenile of other site, or site NOS", "Osteochondritis specified as juvenile of other site, or site NOS", "osteochondrosis not specified as adult or juvenile, of unspecified site", "Osteochondrosis not specified as adult or juvenile, of unspecified site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteochondrosis", "shortest_name_length": 11}
{"curie": "UMLS:C5666801", "names": ["pHGG RTK2", "Diffuse Pediatric-Type High-Grade Glioma RTK2", "Diffuse Pediatric-Type High Grade Glioma RTK2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse Pediatric-Type High Grade Glioma RTK2", "shortest_name_length": 9}
{"curie": "MONDO:0017758", "names": ["disorder of vitamin and non-protein cofactor absorption and transport"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of vitamin and non-protein cofactor absorption and transport", "shortest_name_length": 69}
{"curie": "MONDO:0014260", "names": ["DAVID", "CVID10", "common variable immunodeficiency 10", "immunodeficiency, common variable, 10", "IMMUNODEFICIENCY, COMMON VARIABLE, 10", "NFKB2 common variable immunodeficiency", "immunodeficiency, common variable, type 10", "common variable immunodeficiency caused by mutation in NFKB2", "DEFICIT IN ANTERIOR PITUITARY FUNCTION AND VARIABLE IMMUNODEFICIENCY", "Deficit in anterior pituitary function and variable immunodeficiency", "immunodeficiency, common variable, with central adrenal insufficiency", "IMMUNODEFICIENCY, COMMON VARIABLE, WITH CENTRAL ADRENAL INSUFFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency, common variable, 10", "shortest_name_length": 5}
{"curie": "MONDO:0006961", "names": ["Rida", "rida", "scrapie", "Scrapie", "Scrapie (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scrapie", "shortest_name_length": 4}
{"curie": "UMLS:C0744221", "names": ["friction rub", "Friction rub", "friction rubs", "FRICTION RUB NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Friction rub", "shortest_name_length": 12}
{"curie": "EFO:0010977", "names": ["macrovascular complications of diabetes\"@e"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macrovascular complications of diabetes\"@e", "shortest_name_length": 42}
{"curie": "UMLS:C0856604", "names": ["Rubber sensitivity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rubber sensitivity", "shortest_name_length": 18}
{"curie": "UMLS:C3697982", "names": ["PAH associated with connective tissue disease", "Pulmonary arterial hypertension associated with connective tissue disease", "Pulmonary arterial hypertension associated with connective tissue disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pulmonary arterial hypertension associated with connective tissue disease", "shortest_name_length": 45}
{"curie": "MONDO:0011524", "names": ["DALD", "Dianzani Autoimmune Lymphoproliferative Disease", "DIANZANI AUTOIMMUNE LYMPHOPROLIFERATIVE DISEASE", "Dianzani autoimmune lymphoproliferative disease", "Dianzani autoimmune lymphoproliferative syndrome", "DALD - Dianzani autoimmune lymphoproliferative disease", "Dianzani form of autoimmune lymphoproliferative disease", "Dianzani autoimmune lymphoproliferative disease (disorder)", "Autoimmune Lymphoproliferative Disease without Fas Mutations", "Autoimmune lymphoproliferative syndrome without FAS mutations", "autoimmune lymphoproliferative syndrome without FAS mutations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dianzani autoimmune lymphoproliferative disease", "shortest_name_length": 4}
{"curie": "UMLS:C4054224", "names": ["Pauci-Immune Glomerulonephritis associated with Microscopic Polyangiitis", "Pauci-immune Glomerulonephritis associated with Microscopic Polyangiitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pauci-Immune Glomerulonephritis associated with Microscopic Polyangiitis", "shortest_name_length": 72}
{"curie": "MONDO:0032936", "names": ["MYORIBF", "congenital myopathy 9A", "myopathy, congenital, with respiratory insufficiency and bone fractures", "MYOPATHY, CONGENITAL, WITH RESPIRATORY INSUFFICIENCY AND BONE FRACTURES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy, congenital, with respiratory insufficiency and bone fractures", "shortest_name_length": 7}
{"curie": "MONDO:0021259", "names": ["PROSTATE TUMOR", "prostate tumor", "Prostate Tumor", "Prostate tumor", "prostate tumors", "prostate nodule", "prostate tumours", "Nodular prostate", "PROSTATE NODULAR", "nodular prostate", "prostate neoplasm", "Neoplasm prostate", "Tumor of prostate", "Prostate Neoplasm", "Prostate neoplasm", "Tumor of Prostate", "NEOPLASM PROSTATE", "tumor of prostate", "PROSTATE NEOPLASIA", "Prostate Neoplasms", "Prostate neoplasia", "prostatic neoplasm", "Tumour of prostate", "prostate neoplasms", "Neoplasm, Prostate", "neoplasia prostate", "Prostatic Neoplasm", "Prostatic Neoplasms", "Neoplasm, Prostatic", "Neoplasms, Prostate", "prostatic neoplasms", "Nodular prostate NOS", "Neoplasms, Prostatic", "Neoplasm of prostate", "Neoplasm of Prostate", "prostate gland tumor", "neoplasm of prostate", "NEOPLASM OF PROSTATE", "tumor of the prostate", "Tumor of the Prostate", "Prostatic neoplasm NOS", "tumor of prostate gland", "prostate gland neoplasm", "Neoplasm of the prostate", "Neoplasm of the Prostate", "neoplasm of the prostate", "neoplasm of prostate gland", "NGP - New growth of prostate", "nodular prostate (diagnosis)", "Neoplasm of prostate (disorder)", "prostate gland neoplasm (disease)", "neoplasm of prostate gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate neoplasm", "shortest_name_length": 14}
{"curie": "UMLS:C0432475", "names": ["xx male", "XX Male", "XX males", "xx males", "XX males (disorder)", "karyotype; 46,XX, male", "male with 46,XX karyotype", "Male with 46, XX karyotype", "male with 46,XX karyotype (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "XX males", "shortest_name_length": 7}
{"curie": "UMLS:C1335117", "names": ["Oral Cavity Benign Granular Cell Tumor", "Oral Cavity Benign Granular Cell Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral Cavity Benign Granular Cell Tumor", "shortest_name_length": 38}
{"curie": "MONDO:0008666", "names": ["Malrotation", "Gut malrotation", "midgut volvulus", "Bowel malrotation", "malrotation; bowel", "VOLVULUS OF MIDGUT", "Volvulus of midgut", "Volvulus Of Midgut", "volvulus of midgut", "Malrotation of gut", "bowel; malrotation", "volvulus neonatorum", "Volvulus neonatorum", "Malrotation of bowel", "intestine malrotation", "malrotation intestine", "INTESTINE, MALROTATION", "Intestinal malrotation", "Intestinal Malrotation", "Congenital malrotation", "INTESTINAL MALROTATION", "intestines malrotation", "intestinal malrotation", "Malrotation of the gut", "congenital malrotation", "Malrotation, congenital", "Congenital Malrotations", "Malrotation of the bowel", "Malrotation of intestine", "Congenital malrotation, NOS", "familial intestinal malrotation", "Familial intestinal malrotation", "Incomplete rotation of intestine", "intestinal malrotation, familial", "Intestinal Malrotation, Familial", "INTESTINAL MALROTATION, FAMILIAL", "intestinal malrotation (diagnosis)", "congenital malrotation of intestine", "Congenital Malrotation of Intestine", "Congenital malrotation of intestine", "Familial intestinal malrotation (disorder)", "familial intestinal malrotation (diagnosis)", "Malrotation of intestine with midgut volvulus", "Congenital malrotation of intestine (disorder)", "Congenital malrotation (morphologic abnormality)", "Malrotation of intestine with midgut volvulus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "volvulus of midgut", "shortest_name_length": 11}
{"curie": "MONDO:0017963", "names": ["46,XX DSD induced by endogenous maternal-derived androgen", "46,XX disorder of sex development induced by endogenous maternal-derived androgen"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XX disorder of sex development induced by endogenous maternal-derived androgen", "shortest_name_length": 57}
{"curie": "MONDO:0043123", "names": ["massa casaer ceulemans syndrome", "Massa Casaer Ceulemans syndrome", "arthrogryposis multiplex congenita associated with lissencephaly", "Arthrogryposis multiplex congenita associated with lissencephaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "massa casaer ceulemans syndrome", "shortest_name_length": 31}
{"curie": "UMLS:C0267410", "names": ["THROMBOSIS MESENTERIC ARTERY", "MESENTERIC ARTERY THROMBOSIS", "mesenteric artery thrombosis", "Mesenteric artery thrombosis", "Thrombosis mesenteric artery", "Thrombosis of mesenteric artery", "Thrombosis of mesenteric artery (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thrombosis of mesenteric artery", "shortest_name_length": 28}
{"curie": "MONDO:0006485", "names": ["retroviral disease", "Retrovirus Infection", "retrovirus infection", "infection retrovirus", "retroviral infection", "Retroviral infection", "infection retroviral", "Retroviridae disease", "Retrovirus infection", "carcinosarcoma uterus", "Carcinosarcoma uterus", "Retroviral infections", "Infection, Retrovirus", "Retrovirus Infections", "Retrovirus infections", "uterus carcinosarcoma", "uterine carcinosarcoma", "Infections, Retrovirus", "Retroviridae Infection", "Uterine Carcinosarcoma", "Carcino-sarcoma uterus", "Uterine carcinosarcoma", "Infection, Retroviridae", "carcinosarcoma, uterine", "Retroviridae Infections", "carcinosarcomas uterine", "Carcinosarcoma of uterus", "Retroviral infection NOS", "Infections, Retroviridae", "carcinosarcoma of uterus", "Retrovirus infection NOS", "Disease due to Retroviridae", "Carcinosarcoma of the Uterus", "DISEASES DUE TO RETROVIRIDAE", "carcinosarcoma of the uterus", "Carcinosarcoma of the uterus", "Mullerian tumor, uterine mixed", "Disease caused by Retroviridae", "uterine mixed Mullerian sarcoma", "Mullerian sarcoma, uterine mixed", "retrovirus infection (diagnosis)", "mixed Mullerian sarcoma, uterine", "mixed mullerian sarcoma of uterus", "Carcinosarcoma of uterus (disorder)", "carcinosarcoma of uterus (diagnosis)", "Disease caused by Retroviridae (disorder)", "Malignant mixed Mullerian tumor of uterus", "Malignant mixed Mullerian tumour of uterus", "Uterine Malignant Mixed Mesodermal (Müllerian) Tumor", "uterine malignant mixed mesodermal (Müllerian) tumor", "Uterine Malignant Mixed Mesodermal (Mullerian) Tumor", "uterine malignant mixed mesodermal (Mullerian) tumor", "Malignant Mixed Mesodermal (Müllerian) Tumor of the Uterus", "Malignant Mixed Mesodermal (Mullerian) Tumor of the Uterus", "malignant mixed mesodermal (Mullerian) tumor of the uterus", "malignant mixed mesodermal (Müllerian) tumor of the uterus", "uterine carcinosarcoma/uterine malignant mixed mullerian tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine carcinosarcoma", "shortest_name_length": 18}
{"curie": "MONDO:0019487", "names": ["Myoclonic absence epilepsy", "Myoclonic Absence Epilepsy", "Epilepsy, Myoclonic Absence", "Myoclonic Absence Epilepsies", "epilepsy; myoclonic absences", "Epilepsies, Myoclonic Absence", "myoclonic; epileptic, absences", "epilepsy with myoclonic absences", "Epilepsy with myoclonic absences", "Myoclonic absence epilepsy (disorder)", "Myoclonic absence epilepsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy with myoclonic absences", "shortest_name_length": 26}
{"curie": "MONDO:0030852", "names": ["NEDFASB", "NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SLEEP DISTURBANCE, AND BRAIN ABNORMALITIES", "neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities", "neurodevelopmental disorder wtih dysmorphic facies, sleep disturbance, and brain abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities", "shortest_name_length": 7}
{"curie": "MONDO:0800188", "names": ["malignant hyperthermia, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant hyperthermia, susceptibility to", "shortest_name_length": 41}
{"curie": "UMLS:C5448120", "names": ["Lacrimal Gland Myoepithelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lacrimal Gland Myoepithelial Carcinoma", "shortest_name_length": 38}
{"curie": "MONDO:0016172", "names": ["acquired sensory neuronopathy", "acquired sensory ganglionopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired sensory ganglionopathy", "shortest_name_length": 29}
{"curie": "UMLS:C4527062", "names": ["Clinical Stage III Merkel Cell Carcinoma AJCC v8", "Clinical Stage III Neuroendocrine Carcinoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage III Merkel Cell Carcinoma AJCC v8", "shortest_name_length": 48}
{"curie": "UMLS:C5670708", "names": ["LZTR1 Schwannomatosis 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "LZTR1 Schwannomatosis 2", "shortest_name_length": 23}
{"curie": "UMLS:C1401086", "names": ["PVI", "Peripheral vascular insufficiency", "Peripheral Vascular Insufficiency", "peripheral; vascular insufficiency", "insufficiency; peripheral vascular", "vascular; insufficiency, peripheral", "insufficiency; vascular, peripheral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peripheral Vascular Insufficiency", "shortest_name_length": 3}
{"curie": "MONDO:0020302", "names": ["Angelman syndrome due to maternal monosomy 15q11q13", "Angelman syndrome due to maternal 15q11q13 deletion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Angelman syndrome due to maternal 15q11q13 deletion", "shortest_name_length": 51}
{"curie": "UMLS:C0086405", "names": ["Hereditary sensory neuropathy syndrome", "Hereditary Sensory Radicular Neuropathy", "neuropathy; radicular, hereditary, sensory", "Hereditary sensory neuropathy of Denny-Brown"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hereditary Sensory Radicular Neuropathy", "shortest_name_length": 38}
{"curie": "UMLS:C0178874", "names": ["tumor progression", "Tumor Progression", "Tumor progression", "cancer progression", "Tumour progression", "Neoplasm progression", "neoplasm progression", "neoplastic progression", "Neoplasm progression NOS", "Tumor progression (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tumor Progression", "shortest_name_length": 17}
{"curie": "UMLS:C4087469", "names": ["Myxoid liposarcoma metastatic", "Metastatic Myxoid Liposarcoma", "Metastatic Myxoid/Round Cell Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myxoid liposarcoma metastatic", "shortest_name_length": 29}
{"curie": "MONDO:0021099", "names": ["duct papillomatosis", "Intraductal papillomatosis", "Intraductal Papillomatosis", "intraductal papillomatosis", "Intraductal papillomatosis NOS", "Intraductal papillomatosis, NOS", "Intraductal papillomatosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intraductal papillomatosis", "shortest_name_length": 19}
{"curie": "MONDO:0017545", "names": ["SD1d", "SD1, Castilla type", "syndactyly type 1d", "zygodactyly type 4", "Zygodactyly, Castilla type", "syndactyly type 1, Castilla type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "zygodactyly type 4", "shortest_name_length": 4}
{"curie": "UMLS:C4525127", "names": ["stage IIIC colon cancer", "Stage IIIC Colon Cancer", "Stage IIIC Colon Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Colon Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "MONDO:0019790", "names": ["nms", "NMS", "Neuroleptic malignant", "neuroleptic malignant", "malignant neuroleptic", "neuroleptic malignant syndrome", "malignant neuroleptic syndrome", "Malignant neuroleptic syndrome", "Neuroleptic malignant syndrome", "NEUROLEPTIC MALIGNANT SYNDROME", "Neuroleptic Malignant Syndrome", "syndrome; malignant neuroleptic", "Neuroleptic Malignant Syndromes", "Syndrome, Neuroleptic Malignant", "malignant; neuroleptic syndrome", "Syndromes, Neuroleptic Malignant", "NMS - Neuroleptic malignant syndrome", "NMS (Neuroleptic Malignant Syndrome)", "NMSs (Neuroleptic Malignant Syndrome)", "Neuroleptic malignant syndrome (disorder)", "neuroleptic malignant syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuroleptic malignant syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0012759", "names": ["Camptodactyly syndrome Guadalajara type 3", "camptodactyly syndrome Guadalajara type 3", "camptodactyly syndrome, Guadalajara type 3", "Camptodactyly syndrome, Guadalajara type 3", "camptodactyly syndrome, Guadalajara, type 3", "Camptodactyly Syndrome, Guadalajara, Type III", "camptodactyly syndrome, Guadalajara, type III", "CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III", "Camptodactyly syndrome Guadalajara type 3 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "camptodactyly syndrome, Guadalajara type 3", "shortest_name_length": 41}
{"curie": "UMLS:C0392025", "names": ["Abdomen enlarged", "enlarged abdomen", "ABDOMEN ENLARGED", "Enlarged abdomen", "Enlarged Abdomen", "Enlarging Abdomen", "Enlargement abdomen", "ENLARGEMENT ABDOMEN", "abdomen enlargement", "enlargement abdomen"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Enlargement abdomen", "shortest_name_length": 16}
{"curie": "UMLS:C0235520", "names": ["FEMORAL ARTERY THROMBOSIS", "artery femoral thrombosis", "femoral artery thrombosis", "Femoral artery thrombosis", "thrombosis of femoral artery", "thrombosis; femoral, arterial", "Femoral artery thrombosis (disorder)", "thrombosis of femoral artery (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Femoral artery thrombosis", "shortest_name_length": 25}
{"curie": "MONDO:0007992", "names": ["MICROCORNEA, GLAUCOMA, AND ABSENT FRONTAL SINUSES", "microcornea, glaucoma, and absent frontal sinuses", "Microcornea, glaucoma, and absent frontal sinuses", "microcornea-glaucoma-absent frontal sinuses syndrome", "hereditary microcornea, glaucoma, and absent frontal sinuses", "Hereditary microcornea, glaucoma, and absent frontal sinuses"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcornea-glaucoma-absent frontal sinuses syndrome", "shortest_name_length": 49}
{"curie": "UMLS:C1336117", "names": ["Stage IA Lung Adenocarcinoma", "Stage IA Adenocarcinoma of Lung", "Stage IA Adenocarcinoma of the Lung", "Stage IA Lung Adenocarcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Lung Adenocarcinoma AJCC v7", "shortest_name_length": 28}
{"curie": "UMLS:C4683758", "names": ["Hemoglobin Lepore Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemoglobin Lepore Syndrome", "shortest_name_length": 26}
{"curie": "MONDO:0004063", "names": ["iris mixed cell melanoma", "Intermediate Cell Type Iris Melanoma", "Iris Intermediate Cell Type Melanoma", "Intermediate cell type iris melanoma", "intermediate cell type iris melanoma", "iris intermediate cell type uveal melanoma", "intermediate cell type uveal melanoma of iris"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intermediate cell type iris melanoma", "shortest_name_length": 24}
{"curie": "MONDO:0037742", "names": ["endometrioid stromal and related tumors", "Endometrioid Stromal and Related Tumors", "endometrioid stromal and related neoplasms", "Endometrioid Stromal and Related Neoplasms"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometrioid stromal and related neoplasms", "shortest_name_length": 39}
{"curie": "MONDO:0000739", "names": ["Uvulitis", "uvulitis", "acute uvulitis", "Uvulitis (disorder)", "palatine uvula inflammation", "inflammation of palatine uvula"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uvulitis", "shortest_name_length": 8}
{"curie": "MONDO:0020069", "names": ["Chronic Brain Damage", "chronic brain damage", "chronic encephalitis", "encephalitis, chronic", "Brain Damage, Chronic", "Chronic encephalopathy", "SYNDROME BRAIN CHRONIC", "Chronic Encephalopathy", "ENCEPHALOPATHY CHRONIC", "Encephalopathy chronic", "CHRONIC BRAIN SYNDROME", "brain chronic syndrome", "Chronic brain syndrome", "chronic brain syndrome", "BRAIN SYNDROME CHRONIC", "chronic encephalopathy", "Encephalopathy, Chronic", "Chronic encephalopathy, NOS", "Chronic brain syndrome, NOS", "Chronic brain syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic encephalitis", "shortest_name_length": 20}
{"curie": "MONDO:0001625", "names": ["lutein cyst", "Lutein cyst", "cyst; lutein", "lutein; cyst", "corpus luteum cyst", "Corpus luteum cyst", "Corpus Luteum Cyst", "CORPUS LUTEUM CYST", "corpus cyst luteum", "corpus luteum; cyst", "Corpus Luteum Cysts", "CORPUS LUTEUM, CYST", "Cyst, Corpus Luteum", "corpus luteum cysts", "Cyst, corpus luteum", "Luteal cyst of ovary", "cystic corpus luteum", "Cysts, Corpus Luteum", "Cystic corpus luteum", "cystic; corpus luteum", "corpus luteum; cystic", "Luteal cystic ovary disease", "Corpus luteum cyst (disorder)", "corpus luteum cyst (diagnosis)", "Corpus luteum cyst or hematoma", "corpus luteum ovarian cyst (disease)", "ovarian cyst (disease) of corpus luteum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corpus luteum cyst", "shortest_name_length": 11}
{"curie": "MONDO:0006471", "names": ["Cylindroma of trachea", "Trachea Adenoid Cystic Carcinoma", "trachea adenoid cystic carcinoma", "tracheal adenoid cystic carcinoma", "Tracheal adenoid cystic carcinoma", "Tracheal Adenoid Cystic Carcinoma", "Adenoid cystic carcinoma of trachea", "adenoid cystic carcinoma of trachea", "Adenoid Cystic Carcinoma of Trachea", "adenoid cystic carcinoma of the trachea", "Adenoid cystic carcinoma of the trachea", "Adenoid Cystic Carcinoma of the Trachea", "Adenoid cystic carcinoma of trachea (disorder)", "adenoid cystic carcinoma of trachea (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tracheal adenoid cystic carcinoma", "shortest_name_length": 21}
{"curie": "UMLS:C1883524", "names": ["Valvular Stenosis", "Valvular stenosis", "valvular stenosis NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Valvular stenosis", "shortest_name_length": 17}
{"curie": "MONDO:0004575", "names": ["Choline Deficiency", "choline deficiency", "Choline deficiency", "Deficiency, Choline", "Choline Deficiencies", "Deficiencies, Choline", "choline deficiency disease", "Choline deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choline deficiency disease", "shortest_name_length": 18}
{"curie": "MONDO:0007297", "names": ["FDD", "HOOE", "ADan amyloidosis", "familial Danish dementia", "Familial Danish dementia", "Familial Danish Dementia", "FAMILIAL DANISH DEMENTIA", "dementia, familial Danish", "DEMENTIA, FAMILIAL DANISH", "Dementia, familial Danish", "Familial dementia Danish type", "Familial dementia, Danish type", "familial dementia, Danish type", "Heredopathia Ophthalmootoencephalica", "HEREDOPATHIA OPHTHALMOOTOENCEPHALICA", "Heredopathia ophthalmootoencephalica", "Familial dementia Danish type (disorder)", "Familial dementia, Danish type (diagnosis)", "ITM2B-related cerebral amyloid angiopathy 2", "cerebral amyloid angiopathy, ITM2B-RELATED, 2", "Cerebral Amyloid Angiopathy, Itm2b-Related, 2", "CEREBRAL AMYLOID ANGIOPATHY, ITM2B-RELATED, 2", "cerebral amyloid angiopathy, ITM2B-related, type 2", "cerebellar ataxia, cataract, deafness, and dementia Or psychosis", "CEREBELLAR ATAXIA, CATARACT, DEAFNESS, AND DEMENTIA OR PSYCHOSIS", "cerebellar ataxia, cataract, deafness, and dementia or psychosis", "Cerebellar Ataxia, Cataract, Deafness, and Dementia Or Psychosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ADan amyloidosis", "shortest_name_length": 3}
{"curie": "MONDO:0018221", "names": ["IHF", "Immune HF", "immune HF", "Immune fetal edema", "immune fetal edema", "immune fetal hydrops", "Immune fetal hydrops", "immune hydrops fetalis", "Immune hydrops fetalis", "fetalis hydrops immune", "Immune Hydrops Fetalis", "Hydrops Fetalis, Immune", "Immune hydrops foetalis", "isoimmunized hydrops fetalis", "Hydrops fetalis due to isoimmunisation", "Hydrops fetalis due to isoimmunization", "hydrops; fetal, due to isoimmunization", "Hydrops foetalis due to isoimmunization", "Hydrops foetalis due to isoimmunisation", "isoimmunized hydrops fetalis (diagnosis)", "isoimmunization; fetus, with hydrops fetalis", "Hydrops fetalis due to isoimmunization (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immune hydrops fetalis", "shortest_name_length": 3}
{"curie": "UMLS:C1707293", "names": ["Heart Biphasic Synovial Sarcoma", "Cardiac Biphasic Synovial Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiac Biphasic Synovial Sarcoma", "shortest_name_length": 31}
{"curie": "MONDO:0012435", "names": ["DCMA", "MGA5", "MGA V", "MGCA5", "MGA 5", "Mga, type 5", "MGA, Type V", "MGA, TYPE V", "DCMA syndrome", "3-methylglutaconic aciduria type 5", "3-methylglutaconic aciduria type V", "Dilated Cardiomyopathy with Ataxia", "3-Methylglutaconic Aciduria Type V", "3 methylglutaconic aciduria type V", "dilated cardiomyopathy with ataxia", "3-Methylglutaconic Aciduria Type 5", "Dilated cardiomyopathy with ataxia", "3-METHYLGLUTACONIC ACIDURIA, TYPE V", "3-Methylglutaconic aciduria, type 5", "3-METHYLGLUTACONIC aciduria, type V", "3-Methylglutaconic Aciduria, Type V", "DNAJC19 3-methylglutaconic aciduria", "cardiomyopathy, dilated, with ataxia", "3-@METHYLGLUTACONIC ACIDURIA, TYPE V", "CARDIOMYOPATHY, DILATED, WITH ATAXIA", "Cardiomyopathy, Dilated, with Ataxia", "3 alpha methylglutaconic aciduria type V", "Dilated cardiomyopathy with ataxia syndrome", "3-methylglutaconic aciduria type 5 (disorder)", "3-methylglutaconic aciduria caused by mutation in DNAJC19"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "3-methylglutaconic aciduria type 5", "shortest_name_length": 4}
{"curie": "UMLS:C5557648", "names": ["Large Solitary Luteinized Follicle Cyst of Ovary", "Large Solitary Luteinized Follicular Cyst of Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Large Solitary Luteinized Follicle Cyst of Ovary", "shortest_name_length": 48}
{"curie": "UMLS:C0549584", "names": ["Subcutaneous Disorder", "Subcutaneous Disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subcutaneous Disorder", "shortest_name_length": 21}
{"curie": "UMLS:C4054387", "names": ["Epstein-Barr Virus Associated Nephrotic Syndrome", "Nephrotic Syndrome - Epstein-Barr Virus Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - Epstein-Barr Virus Associated", "shortest_name_length": 48}
{"curie": "UMLS:C4528638", "names": ["Stage III Lentigo Maligna AJCC v7", "Stage III Lentigo Maligna Melanoma", "Stage III Lentigo Maligna Melanoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Lentigo Maligna Melanoma AJCC v7", "shortest_name_length": 33}
{"curie": "UMLS:C2609173", "names": ["Gasping Syndrome", "Gasping syndrome", "Neonatal Gasping Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gasping syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0009450", "names": ["Ciliary Dyskinesia With Excessively Long Cilia", "ciliary dyskinesia with excessively long cilia", "CILIARY DYSKINESIA WITH EXCESSIVELY LONG CILIA", "Immotile Cilia Syndrome Due To Excessively Long Cilia", "IMMOTILE CILIA SYNDROME DUE TO EXCESSIVELY LONG CILIA", "immotile cilia syndrome due to excessively long cilia", "Immotile cilia syndrome due to excessively long cilia", "Immotile cilia syndrome, due to excessively long cilia", "Immotile cilia syndrome due to excessively long cilia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ciliary dyskinesia with excessively long cilia", "shortest_name_length": 46}
{"curie": "UMLS:C4761513", "names": ["Recurrent Ependymoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Ependymoma", "shortest_name_length": 20}
{"curie": "UMLS:C1882972", "names": ["Low Grade Salivary Duct Carcinoma", "Salivary Gland Intraductal Carcinoma", "Salivary Gland Low Grade Cribriform Cystadenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Salivary Gland Intraductal Carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0003587", "names": ["Liposarcoma", "liposarcoma", "childhood liposarcoma", "Childhood Liposarcoma", "Pediatric Liposarcoma", "pediatric liposarcoma", "liposarcoma, childhood", "liposarcoma, pediatric", "sarcoma, lipo-, childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pediatric liposarcoma", "shortest_name_length": 11}
{"curie": "UMLS:C5669862", "names": ["Locally Advanced Nasal Cavity Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Nasal Cavity Squamous Cell Carcinoma", "shortest_name_length": 53}
{"curie": "MONDO:0008388", "names": ["hair ring", "RINGED HAIR", "Ringed hair", "ringed hair", "PILI ANNULATI", "annulati pili", "pili annulati", "Pili annulati", "Ringed hair disease", "ringed hair disease", "pili; annulati or torti", "annulati or torti; pili", "Pili annulati (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ringed hair disease", "shortest_name_length": 9}
{"curie": "MONDO:0014436", "names": ["BBS8", "BARDET-BIEDL SYNDROME 8", "Bardet-Biedl syndrome 8", "Bardet-Biedl Syndrome 8", "TTC8 Bardet-Biedl syndrome", "Bardet-Biedl syndrome type 8", "Bardet-Biedl syndrome caused by mutation in TTC8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bardet-Biedl syndrome 8", "shortest_name_length": 4}
{"curie": "MONDO:0100262", "names": ["PEX5 related Zellweger spectrum disorder", "peroxisome biogenesis disorder due to PEX5 defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder due to PEX5 defect", "shortest_name_length": 40}
{"curie": "MONDO:0011133", "names": ["Warburg Thomsen syndrome", "Warburg-Thomsen syndrome", "Yemenite deaf-blind hypopigmentation syndrome", "YEMENITE DEAF-BLIND HYPOPIGMENTATION SYNDROME", "Deaf blind hypopigmentation syndrome Yemenite type", "deaf blind hypopigmentation syndrome, Yemenite type", "Deaf blind hypopigmentation syndrome, Yemenite type", "Yemenite (Warburg) deaf-blind hypopigmentation syndrome", "Deaf blind hypopigmentation syndrome Yemenite type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deaf blind hypopigmentation syndrome, Yemenite type", "shortest_name_length": 24}
{"curie": "UMLS:C1400817", "names": ["Infectious Meningoencephalitis", "infectious; meningoencephalitis", "meningoencephalitis; infectious"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infectious Meningoencephalitis", "shortest_name_length": 30}
{"curie": "MONDO:0006973", "names": ["Adnexal Carcinoma", "Adnexal carcinoma", "adnexal carcinoma", "carcinoma of adnexa", "Carcinoma of Adnexa", "skin adnexal carcinoma", "skin appendage carcinoma", "Skin appendage carcinoma", "Skin Appendage Carcinoma", "Skin Appendage Carcinomas", "Carcinoma, Skin Appendage", "Appendage Carcinoma, Skin", "Carcinomas, Skin Appendage", "Appendage Carcinomas, Skin", "Carcinoma of Skin Appendage", "carcinoma of skin appendage", "CARCINOMA, ADNEXAL, MALIGNANT", "carcinoma, adnexal, malignant", "cutaneous appendage carcinoma", "carcinoma of cutaneous appendage", "skin appendage carcinoma (diagnosis)", "Skin appendage carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin appendage carcinoma", "shortest_name_length": 17}
{"curie": "MONDO:0016861", "names": ["Alagille syndrome due to del(20)(p12)", "Alagille syndrome due to monosomy 20p12", "Alagille syndrome due to 20p12 microdeletion", "Arteriohepatic dysplasia due to monosomy 20p12", "Alagille-Watson syndrome due to monosomy 20p12", "syndromic bile duct paucity due to monosomy 20p12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alagille syndrome due to 20p12 microdeletion", "shortest_name_length": 37}
{"curie": "UMLS:C0854982", "names": ["Large cell lung cancer stage IV", "Stage IV Large Cell Lung Cancer", "Stage IV Large Cell Lung Carcinoma", "Stage IV Large Cell Carcinoma of Lung", "Stage IV Large Cell Carcinoma of the Lung", "Stage IV Lung Large Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Large cell lung cancer stage IV", "shortest_name_length": 31}
{"curie": "MONDO:0018830", "names": ["kimura disease", "Kimura disease", "KIMURA DISEASE", "Kimura Disease", "Kimuras Disease", "Disease, Kimura", "kimura's disease", "Kimura's Disease", "Kimura's disease", "Disease, Kimura's", "Kimura's Diseases", "Kimura's disease (disorder)", "eosinophilic lymphogranuloma", "Eosinophilic lymphogranuloma", "Eosinophilic Lymphofolliculosis", "eosinophilic lymphofolliculosis", "Eosinophilic Lymphofolliculoses", "Lymphofolliculosis, Eosinophilic", "Eosinophilic Granuloma of Soft Tissue", "eosinophilic granuloma of soft tissue", "eosinophilic lymphofollicular granuloma", "Eosinophilic Lymphofollicular Granuloma", "Granuloma, Eosinophilic Lymphofollicular", "Eosinophilic Lymphofollicular Granulomas", "Lymphofollicular Granuloma, Eosinophilic", "Eosinophilic Hyperplastic Lymphogranuloma", "eosinophilic hyperplastic lymphogranuloma", "Lymphogranuloma, Eosinophilic Hyperplastic", "Eosinophilic Hyperplastic Lymphogranulomas", "Hyperplastic Lymphogranuloma, Eosinophilic", "angiolymphoid hyperplasia with eosinophilia", "Angiolymphoid Hyperplasia with Eosinophilia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kimura disease", "shortest_name_length": 14}
{"curie": "MONDO:0030854", "names": ["OIEDS1", "OIEDS SYNDROME 1", "OIEDS Syndrome 1", "combined osteogenesis imperfecta and Ehlers-Danlos syndrome 1", "COMBINED OSTEOGENESIS IMPERFECTA AND EHLERS-DANLOS SYNDROME 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined osteogenesis imperfecta and Ehlers-Danlos syndrome 1", "shortest_name_length": 6}
{"curie": "UMLS:C1332258", "names": ["Anal Adenocarcinoma within Anorectal Fistula", "Adenocarcinoma of Anus within Anorectal Fistula", "Adenocarcinoma of the Anus within Anorectal Fistula"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anal Adenocarcinoma within Anorectal Fistula", "shortest_name_length": 44}
{"curie": "MONDO:0005113", "names": ["bacterial disease", "Bacterial Disease", "Bacterial disease", "bacterial; disease", "bacterial disorder", "Bacterial diseases", "bacterial diseases", "Bacterial Diseases", "Bacterial Disorder", "Infection bacterial", "Bacterial Disorders", "Bacterial infection", "INFECTION BACTERIAL", "Infection;bacterial", "BACTERIAL INFECTION", "bacterial infection", "Bacterial Infection", "Infection, Bacterial", "infection; bacterial", "Bacterial Infections", "bacterial; infection", "infection, bacterial", "bacterial infections", "Bacterial infections", "infections, bacterial", "Infections, Bacterial", "bacteria caused disease", "Bacterial infection NOS", "bacteria caused diseases", "Bacterial infection, NOS", "other bacterial infection", "Disease caused by bacteria", "disease caused by bacteria", "Bacteria infectious disease", "bacterial infection by site", "Diseases Caused by Bacteria", "Bacterial infectious disease", "Bacterial Infectious Disease", "Bacteria disease or disorder", "bacterial infectious disease", "BACTERIAL INFECTIOUS DISEASES", "bacterial infectious diseases", "Bacterial infectious disorders", "Disease caused by bacteria, NOS", "bacterial infection (diagnosis)", "Bacterial infection, unspecified", "disease (or disorder); bacterial", "Bacterial infectious disease, NOS", "Bacteria caused disease or disorder", "Bacterial infection; unspecified site", "bacterial infection by site (diagnosis)", "Bacterial infectious disease (disorder)", "Bacterial infection of unspecified site", "BACTERIAL INFECTIOUS DISEASES: GENERAL TERMS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bacterial infectious disease", "shortest_name_length": 17}
{"curie": "MONDO:0012420", "names": ["DFNB49", "autosomal recessive deafness 49", "deafness, autosomal recessive 49", "DEAFNESS, AUTOSOMAL RECESSIVE 49", "Deafness, Autosomal Recessive 49", "deafness, autosomal recessive type 49", "autosomal recessive nonsyndromic deafness 49", "autosomal recessive nonsyndromic hearing loss 49", "autosomal recessive nonsyndromic deafness type 49", "MARVELD2 autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic deafness caused by mutation in MARVELD2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 49", "shortest_name_length": 6}
{"curie": "UMLS:C0861834", "names": ["Duodenal cancer recurrent", "Recurrent Malignant Duodenal Neoplasm", "Malignant neoplasm of duodenum recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Duodenal cancer recurrent", "shortest_name_length": 25}
{"curie": "MONDO:0060510", "names": ["COGIS", "Cohen-Gibson syndrome", "COHEN-GIBSON SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cohen-Gibson syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0011953", "names": ["ANE", "ANE1", "ADANE", "IIAE3", "acute necrotizing encephalopathy type 1", "infection-induced acute encephalopathy 3", "familial acute necrotizing encephalopathy", "Familial acute necrotizing encephalopathy", "Familial acute necrotising encephalopathy", "Recurrent acute necrotizing encephalopathy", "recurrent acute necrotizing encephalopathy", "Recurrent acute necrotising encephalopathy", "susceptibility to acute necrotizing encephalopathy", "autosomal dominant acute necrotizing encephalopathy", "encephalopathy, acute necrotizing, susceptibility to", "ENCEPHALOPATHY, ACUTE NECROTIZING, SUSCEPTIBILITY TO", "Familial acute necrotizing encephalopathy (disorder)", "susceptibility to infection-induced acute encephalopathy 3", "susceptibility to acute infection-induced encephalopathy-3", "Postinfectious acute necrotizing hemorrhagic encephalopathy", "ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3", "encephalopathy, acute, infection-induced, susceptibility to, 3", "encephalopathy, acute, infection-induced, 3, susceptibility to", "encephalopathy, acute, infection-induced, susceptibility to, type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial acute necrotizing encephalopathy", "shortest_name_length": 3}
{"curie": "MONDO:0011144", "names": ["CLN6", "CLN6A", "vLINCL", "CLN6 disease", "neuronal ceroid lipofuscinosis 6", "neuronal ceroid lipofuscinosis 6A", "ceroid lipofuscinosis, neuronal, 6", "Ceroid Lipofuscinosis, Neuronal, 6", "CEROID LIPOFUSCINOSIS, NEURONAL, 6", "ceroid lipofuscinosis, neuronal, 6A", "CEROID LIPOFUSCINOSIS, NEURONAL, 6A", "neuronal ceroid lipofuscinosis type 6", "CLN6 disease, late infantile (subtype)", "ceroid lipofuscinosis, neuronal, type 6", "CLN6 disease, adult Kufs type A (subtype)", "CLN6 late infantile neuronal ceroid lipofuscinosis", "neuronal ceroid lipofuscinosis 6 variable age of onset", "Neuronal Ceroid Lipofuscinosis, Late Infantile, Variant", "NEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, VARIANT", "neuronal ceroid lipofuscinosis, late infantile, variant", "ceroid lipofuscinosis, neuronal, 6, variable age at onset", "Ceroid Lipofuscinosis, Neuronal, 6, Variable Age At Onset", "neuronal ceroid lipofuscinosis, Gypsy/Indian early juvenile variant", "late infantile neuronal ceroid lipofuscinosis caused by mutation in CLN6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ceroid lipofuscinosis, neuronal, 6A", "shortest_name_length": 4}
{"curie": "MONDO:0018655", "names": ["hypomyelination-cerebellar atrophy-hypoplasia of the corpus callosum syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypomyelination-cerebellar atrophy-hypoplasia of the corpus callosum syndrome", "shortest_name_length": 77}
{"curie": "MONDO:0010395", "names": ["GOUT, PRPS-RELATED", "Gout, PRPS-Related", "gout, PRPS-related", "PRPS1 superactivity", "PRPS1 SUPERACTIVITY", "PRPP synthetase superactivity", "gout, PRPS-related, X-linked recessive", "phosphoribosylpyrophosphate synthetase superactivity", "Phosphoribosylpyrophosphate synthetase superactivity", "Phosphoribosylpyrophosphate Synthetase Superactivity", "PHOSPHORIBOSYLPYROPHOSPHATE SYNTHETASE SUPERACTIVITY", "Phosphoribosyl pyrophosphate synthetase superactivity", "Phosphoribosylpyrophosphate synthetase superactivity (disorder)", "phosphoribosylpyrophosphate synthetase superactivity (diagnosis)", "phosphoribosylpyrophosphate synthetase superactivity, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phosphoribosylpyrophosphate synthetase superactivity", "shortest_name_length": 18}
{"curie": "UMLS:C0153691", "names": ["Adrenal metastases", "adrenal metastases", "Suprarenal metastasis", "Metastases to Adrenals", "Metastases to adrenals", "Metastasis to Adrenals", "adrenal gland metastasis", "metastasis to adrenal gland", "Metastasis to adrenal gland", "Metastatic Tumor to the Adrenals", "Cancer metastatic to adrenal gland", "Metastatic Neoplasm to the Adrenals", "adrenal neoplasm malignant secondary", "Metastatic Tumor to the Adrenal Gland", "Metastatic Neoplasm to the Adrenal Gland", "Secondary malignant neoplasm of adrenal gland", "secondary malignant neoplasm of adrenal gland", "Metastatic malignant neoplasm of adrenal gland", "Metastatic malignant neoplasm to adrenal gland", "Secondary malignant neoplasm of suprarenal gland", "metastasis of malignant neoplasm to adrenal gland", "Metastatic Malignant Neoplasm in the Adrenal Gland", "Metastatic Malignant Neoplasm to the Adrenal Gland", "Metastatic malignant neoplasm to adrenal gland (disorder)", "secondary malignant neoplasm of adrenal gland (diagnosis)", "metastasis of malignant neoplasm to adrenal gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to adrenal gland", "shortest_name_length": 18}
{"curie": "UMLS:C0014412", "names": ["EXPOSURE ENVIRONMENTAL", "environmental exposure", "Environmental exposure", "Environmental Exposure", "Environmental Exposures", "environmental exposures", "Exposure, Environmental", "Exposures, Environmental"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Environmental Exposure", "shortest_name_length": 22}
{"curie": "UMLS:C2936380", "names": ["Neointima", "Neointimas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neointima", "shortest_name_length": 9}
{"curie": "MONDO:0016800", "names": ["mitochondrial membrane transport disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial membrane transport disorder", "shortest_name_length": 41}
{"curie": "MONDO:0011654", "names": ["KONDOH SYNDROME", "Kondoh syndrome", "Kondoh Syndrome", "MENTAL RETARDATION, MICROCEPHALY, GROWTH RETARDATION, JOINT CONTRACTURES, AND FACIAL DYSMORPHISM", "mental retardation, microcephaly, growth retardation, JOINT contractures, and facial dysmorphism", "Mental Retardation, Microcephaly, Growth Retardation, Joint Contractures, and Facial Dysmorphism", "intellectual disability, microcephaly, growth retardation, JOINT contractures, and facial dysmorphism", "intellectual disability, microcephaly, growth retardation, joint contractures, and facial dysmorphism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, microcephaly, growth retardation, joint contractures, and facial dysmorphism", "shortest_name_length": 15}
{"curie": "UMLS:C2931591", "names": ["JSSc", "Juvenile Systemic Sclerosis", "Juvenile Systemic Scleroderma", "Juvenile systemic scleroderma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Juvenile systemic scleroderma", "shortest_name_length": 4}
{"curie": "UMLS:C4086164", "names": ["Childhood Mixed Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Mixed Germ Cell Tumor", "shortest_name_length": 31}
{"curie": "MONDO:0009361", "names": ["Aqueduct stenosis", "aqueduct stenosis", "Aqueductal Stenoses", "Aqueductal Stenosis", "aqueductal stenosis", "Aqueductal stenosis", "AQUEDUCTAL STENOSIS", "Stenoses, Aqueductal", "Stenosis, Aqueductal", "aqueduct of stenosis sylvius", "Aqueduct of Sylvius stenosis", "aqueduct of Sylvius; stenosis", "stenosis; aqueduct of Sylvius", "Stenosis of aqueduct of Sylvius", "Narrowing of aqueduct of Sylvius", "Stenosis of the aqueduct of Sylvius", "Congenital stenosis, aqueduct of Sylvius", "Congenital stenosis of aqueduct of Sylvius", "congenital stenosis of aqueduct of Sylvius", "Congenital stenosis of aqueduct of Sylvius (disorder)", "congenital stenosis of aqueduct of Sylvius (diagnosis)", "hydrocephalus due to congenital stenosis of aqueduct of Sylvius", "autosomal recessive hydrocephalus due to congenital stenosis of aqueduct of Sylvius"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive hydrocephalus due to congenital stenosis of aqueduct of Sylvius", "shortest_name_length": 17}
{"curie": "MONDO:0035584", "names": ["punctate inner choroidopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "punctate inner choroidopathy", "shortest_name_length": 28}
{"curie": "MONDO:0005962", "names": ["tb bone", "bone tb", "bones tb", "skeletal tuberculosis", "cartilage; tuberculous", "Osteoarticular Tuberculoses", "osteoarticular tuberculosis", "Osteoarticular Tuberculosis", "tuberculosis osteoarticular", "Tuberculoses, Osteoarticular", "tuberculosis of bones joints", "Tuberculosis, Osteoarticular", "TUBERCULOSIS OF BONES AND JOINTS", "Tuberculosis of bones and joints", "Tuberculosis of bones and/or joints", "Tuberculosis of bones and joints, NOS", "Tuberculosis of unspecified bones and joints", "Tuberculosis of bones and/or joints (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skeletal tuberculosis", "shortest_name_length": 7}
{"curie": "UMLS:C5548439", "names": ["MLA", "Mesonephric-like adenocarcinoma", "Mesonephric-Like Adenocarcinoma", "Mesonephric-like adenocarcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mesonephric-like adenocarcinoma", "shortest_name_length": 3}
{"curie": "MONDO:0019888", "names": ["Trisomy 20qter", "trisomy 20qter", "distal trisomy 20q", "Distal trisomy 20q", "Distal duplication 20q", "distal duplication 20q", "distal trisomy type 20q", "telomeric duplication 20q", "Telomeric duplication 20q", "Distal trisomy 20q syndrome", "Distal trisomy 20q (diagnosis)", "Distal trisomy 20q syndrome (disorder)", "anomaly of chromosome pair 20 partial trisomy 20q distal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal trisomy 20q", "shortest_name_length": 14}
{"curie": "MONDO:0000251", "names": ["motility-related diarrhea", "diarrhea secondary to altered bowel motility", "diarrheal disease secondary to altered bowel motility"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diarrheal disease secondary to altered bowel motility", "shortest_name_length": 25}
{"curie": "UMLS:C3501835", "names": ["Genetic Emphysema", "Inherited emphysema", "Inherited Emphysema", "Alpha-1 Related Emphysema", "Hereditary Pulmonary Emphysema", "Alpha-1 Protease Inhibitor Deficiency", "alpha-1-Antitrypsin Deficiency, Autosomal Recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alpha-1-Antitrypsin Deficiency, Autosomal Recessive", "shortest_name_length": 17}
{"curie": "UMLS:C4743574", "names": ["Silent Corticotroph Adenoma Type 2", "Nonfunctional Corticotroph Adenoma Type 2", "Sparsely Granulated Silent Corticotroph Adenoma", "Sparsely Granulated Nonfunctional Corticotroph Adenoma", "Non-Functioning Sparsely Granulated Corticotroph Adenoma", "Non-Functioning Sparsely Granulated Corticotroph Pituitary Neuroendocrine Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Functioning Sparsely Granulated Corticotroph Pituitary Neuroendocrine Tumor", "shortest_name_length": 34}
{"curie": "MONDO:0019563", "names": ["lSSc", "CREST", "crest", "lcSSc", "CRST SYNDROME", "crst syndrome", "CRST syndrome", "CRST Syndrome", "CREST SYNDROME", "CRST Syndromes", "CREST Syndrome", "Syndrome, CRST", "CREST syndrome", "CRST syndromes", "crest syndrome", "syndrome, CREST", "Syndrome, CREST", "CREST Syndromes", "CR(E)ST syndrome", "crest syndrome (diagnosis)", "CREST VARIANT OF SCLERODERMA", "limited cutaneous Systemic sclerosis", "Limited Cutaneous Systemic Sclerosis", "Limited Cutaneous Systemic Scleroderma", "limited cutaneous Systemic Scleroderma", "Calcinosis-Raynaud Phenomenon-Sclerodactyly-Telangiectasia", "calcinosis Raynaud phenomenon sclerodactyly telangiectasia", "Calcinosis-Raynaud's sclerodactyly-telangiectasia syndrome", "Calcinosis Raynaud Phenomenon Sclerodactyly Telangiectasia", "calcinosis-Raynaud phenomenon-sclerodactyly-telangiectasia", "phenomenon-sclerodactyly-telangiectasia, calcinosis-Raynaud", "Phenomenon-Sclerodactyly-Telangiectasia, Calcinosis-Raynaud", "Calcinosis cutis, Raynaud's, sclerodactyly AND telangiectasia", "Calcinosis cutis, Raynaud's, sclerodactyly and telangiectasia", "Calcinosis, Raynaud's phenomenon, sclerodactyly, telangiectasia syndrome", "Calcinosis, Raynaud's phenomenon, sclerodactyly, and telangiectasia syndrome", "CRST - Calcinosis, Raynaud's phenomenon, sclerodactyly, telangiectasia syndrome", "Calcinosis, Raynaud phenomenon, sclerodactyly, and telangiectasia (CRST) syndrome", "Calcinosis, Raynaud's phenomenon, sclerodactyly, and telangiectasia (CRST) syndrome", "Calcinosis cutis, Raynaud's, esophageal dysfunction, sclerodactyly and telangiectasia", "Calcinosis cutis, Raynaud's, esophageal dysfunction, sclerodactyly AND telangiectasia", "Calcinosis cutis, Raynaud's, oesophageal dysfunction, sclerodactyly and telangiectasia", "Calcinosis cutis, Raynaud's, oesophageal dysfunction, sclerodactyly AND telangiectasia", "Calcinosis, Raynaud's phenomenon, sclerodactyly, and telangiectasia syndrome (disorder)", "calcinosis - Raynaud phenomenon - esophageal involvement - sclerodactyly - telangiectasia", "calcinosis-Raynaud phenomenon-esophageal involvement-sclerodactyly-telangiectasia syndrome", "CREST - Calcinosis, Raynaud's phenomenon, esophageal dysfunction, sclerodactyly, telangiectasia", "Calcinosis, Raynaud's phenomenon, sclerodactyly, esophageal dysfunction, telangiectasia syndrome", "calcinosis, Raynaud's phenomenon, esophageal dismobility, sclerodactyly, telangiectasia syndrome", "CREST - Calcinosis, Raynaud's phenomenon, oesophageal dysfunction, sclerodactyly, telangiectasia", "Calcinosis, Raynaud's phenomenon, Esophageal dismobility, Sclerodactyly, Telangiectasia Syndrome", "Calcinosis, Raynaud's phenomenon, sclerodactyly, oesophageal dysfunction, telangiectasia syndrome", "Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome", "Calcinosis, Raynaud's phenomenon, oesophageal dysmotility, sclerodactyly, and telangiectasia syndrome", "CREST - Calcinosis, Raynaud's phenomenon, sclerodactyly, esophageal involvement, telangiectasia syndrome", "CREST - Calcinosis, Raynaud's phenomenon, sclerodactyly, oesophageal involvement, telangiectasia syndrome", "Calcinosis, Raynaud phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome", "Calcinosis, Raynaud phenomenon, oesophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome", "Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome", "Calcinosis, Raynaud's phenomenon, oesophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome", "Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CREST syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0002950", "names": ["Clear Cell Basal Cell Carcinoma", "clear cell basal cell carcinoma", "Skin Clear Cell Basal Cell Carcinoma", "skin clear cell basal cell carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin clear cell basal cell carcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C3272603", "names": ["Colorectal Neuroendocrine Neoplasm", "Large Intestinal Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Neuroendocrine Neoplasm", "shortest_name_length": 34}
{"curie": "UMLS:C4763925", "names": ["Maternal Hemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Maternal Hemorrhage", "shortest_name_length": 19}
{"curie": "UMLS:C0269126", "names": ["second degree uterine prolapse", "Second degree uterine prolapse", "Second Degree Uterine Prolapse", "Uterine prolapse, second degree", "uterus; prolapse, second degree", "prolapse; uterus, second degree", "Second degree uterine prolapse (disorder)", "second degree uterine prolapse (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Second degree uterine prolapse", "shortest_name_length": 30}
{"curie": "MONDO:0017935", "names": ["hyperinsulinism due to HNF1A deficiency", "Hyperinsulinism due to HNF1A deficiency", "Hyperinsulinemic hypoglycemia due to HNF1A deficiency", "hyperinsulinemic hypoglycemia due to HNF1A deficiency", "Hyperinsulinism due to hepatocyte nuclear factor 1-alpha deficiency", "Hyperinsulinism due to hepatocyte nuclear factor 1-alpha deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperinsulinism due to HNF1A deficiency", "shortest_name_length": 39}
{"curie": "UMLS:C0041343", "names": ["tuboovarian abscess", "TUBOOVARIAN ABSCESS", "abscess tubo-ovarian", "tubo-ovarian abscess", "Tubo ovarian abscess", "Tubo-ovarian abscess", "Tubo-Ovarian Abscess", "ABSCESS, TUBO-OVARIAN", "Tubo-ovarian abscess (disorder)", "tubo-ovarian abscess (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tubo-ovarian abscess", "shortest_name_length": 19}
{"curie": "UMLS:C5205877", "names": ["Liver Radiation Injury", "LIVER RADIATION INJURY", "Hepatic Radiation Injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liver Radiation Injury", "shortest_name_length": 22}
{"curie": "UMLS:C0263115", "names": ["axillary abscess", "AXILLARY ABSCESS", "Axillary abscess", "Axillary Abscess", "Abscess of axilla", "abscess of axilla", "Abscess of axilla (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abscess of axilla", "shortest_name_length": 16}
{"curie": "MONDO:0009226", "names": ["FBCG1", "FIBROCHONDROGENESIS 1", "fibrochondrogenesis 1", "fibrochondrogenesis type 1", "COL11A1 fibrochondrogenesis", "fibrochondrogenesis caused by mutation in COL11A1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibrochondrogenesis 1", "shortest_name_length": 5}
{"curie": "MONDO:0012300", "names": ["HPC6", "PROSTATE CANCER, HEREDITARY, 6", "Prostate Cancer, Hereditary, 6", "prostate cancer, hereditary, 6", "prostate cancer, susceptibility to", "prostate cancer, hereditary, type 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate cancer, hereditary, 6", "shortest_name_length": 4}
{"curie": "UMLS:C0236073", "names": ["CEREBELLAR INFARCTION", "Cerebellar infarction", "infarction; cerebellar", "cerebellar; infarction", "Cerebellar infarction (disorder)", "Cerebellar infarction (diagnosis)", "cerebral infarction posterior circulation cerebellar"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebellar infarction", "shortest_name_length": 21}
{"curie": "MONDO:0005574", "names": ["tauopathy", "Tauopathy", "Tauopathies", "tauopathies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tauopathy", "shortest_name_length": 9}
{"curie": "MONDO:0000250", "names": ["Osmotic diarrhea", "osmotic diarrhea", "Osmotic diarrhoea", "permeability diarrhea", "Permeability diarrhea", "Permeability diarrhoea", "osmotic diarrheal disease", "Osmotic diarrhea (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osmotic diarrheal disease", "shortest_name_length": 16}
{"curie": "UMLS:C0855090", "names": ["Refractory B-Cell Lymphoma", "B-Cell Lymphoma Refractory", "B-cell lymphoma refractory", "Refractory B-Cell Non-Hodgkin Lymphoma", "Refractory B-Cell Non-Hodgkin's Lymphoma", "B-cell non-Hodgkin's lymphoma refractory"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-cell lymphoma refractory", "shortest_name_length": 26}
{"curie": "UMLS:C0398686", "names": ["immunodeficiency primary", "primary immunodeficiency", "Primary immunodeficiency", "Primary Immune Deficiency", "Deficiency, Primary Immune", "Immune Deficiency, Primary", "immunodeficiencies primary", "Primary Immune Deficiencies", "Primary Immunodeficiency Disease", "Primary Immunodeficiency Disorder", "Primary Immunodeficiency Diseases", "Immunodeficiency Disease, Primary", "Primary immunodeficiency syndrome", "Primary Immunodeficiency Syndrome", "Primary Immune Deficiency Disease", "Primary Immunodeficiency Disorders", "Primary immune deficiency disorder", "primary immune deficiency disorder", "Immunodeficiency Syndrome, Primary", "Immunodeficiency Diseases, Primary", "Primary Immunodeficiency Syndromes", "Primary immunodeficiency syndromes", "Primary Immune Deficiency Syndrome", "Primary Immune Deficiency Diseases", "Primary Immune Deficiency Disorder", "Immunodeficiency Disorder, Primary", "Primary Immune Deficiency Disorders", "Immune deficiency disorder, primary", "Primary Immune Deficiency Syndromes", "Immunodeficiency Syndromes, Primary", "Primary immune deficiency disorder, NOS", "Primary immune deficiency disorder (disorder)", "primary immune deficiency disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary immune deficiency disorder", "shortest_name_length": 24}
{"curie": "UMLS:C1711314", "names": ["Early Favorable Non-Hodgkin Lymphoma", "Early Favorable Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Early Favorable Non-Hodgkin Lymphoma", "shortest_name_length": 36}
{"curie": "MONDO:0008535", "names": ["HHT", "HHT1", "ORW disease", "Osler-Rendu-Weber disease", "Osler Weber Rendu syndrome type 1", "hereditary hemorrhagic telangiectasia type 1", "TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1", "Telangiectasia, Hereditary Hemorrhagic, Type 1", "telangiectasia, hereditary hemorrhagic, type 1", "ENG-related Hereditary hemorrhagic telangiectasia", "telangiectasia, hereditary hemorrhagic, of RENDU, Osler, and WEBER", "telangiectasia, hereditary hemorrhagic, of Rendu, Osler, and Weber"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "telangiectasia, hereditary hemorrhagic, type 1", "shortest_name_length": 3}
{"curie": "MONDO:0010090", "names": ["Summitt syndrome", "SUMMITT SYNDROME", "Summitt syndrome (disorder)", "Summitt's acrocephalosyndactyly", "Recessive acrocephalosyndactyly with normal intelligence", "recessive acrocephalosyndactyly with normal intelligence"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Summitt syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0005485", "names": ["PSYCHOSES", "Psychotic", "PSYCHOSIS", "Psychosis", "Psychoses", "psychoses", "psychosis", "psychotic", "psychosis nos", "Psychosis NOS", "Psychosis, NOS", "mental disorder", "General Psychoses", "Atypical psychosis", "psychotic disorder", "Psychotic disorder", "PSYCHOSIS ATYPICAL", "Atypical Psychoses", "atypical psychosis", "PSYCHOTIC DISORDER", "Psychotic Disorder", "ATYPICAL PSYCHOSIS", "psychotic; disorder", "psychotic disorders", "Psychosis, atypical", "disorder; psychotic", "Disorder, Psychotic", "Psychotic Disorders", "Disorders, Psychotic", "Unspecified psychosis", "psychosis (diagnosis)", "psychotic disorder nos", "PSYCHOTIC DISORDER NOS", "Psychotic disorder NOS", "Psychotic disorder, NOS", "Psychotic disorder (disorder)", "atypical psychosis (diagnosis)", "psychotic disorder (diagnosis)", "mental or behavioural disorder", "Other and unspecified reactive psychosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "psychotic disorder", "shortest_name_length": 9}
{"curie": "UMLS:C0742078", "names": ["brain mass", "Brain Mass", "Brain mass", "BRAIN MASS", "CEREBRAL MASS", "cerebral mass", "cerebral masses", "Mass lesion of brain", "Mass lesion of brain (finding)", "Space-occupying lesion of brain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mass lesion of brain", "shortest_name_length": 10}
{"curie": "MONDO:0009687", "names": ["Myasthenia, Congenital, Refractory to Acetylcholinesterase Inhibitors", "myasthenia, congenital, refractory to acetylcholinesterase inhibitors", "MYASTHENIA, CONGENITAL, REFRACTORY TO ACETYLCHOLINESTERASE INHIBITORS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myasthenia, congenital, refractory to acetylcholinesterase inhibitors", "shortest_name_length": 69}
{"curie": "UMLS:C3640071", "names": ["Suspected Necrotizing Enterocolitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Suspected Necrotizing Enterocolitis", "shortest_name_length": 35}
{"curie": "UMLS:C2919502", "names": ["IgA Nephropathy, Familal", "IgA Nephropathy, Familial", "Familial immunoglobulin A nephropathy", "Familial immunoglobulin A (IgA) nephropathy", "Familial immunoglobulin A nephropathy (disorder)", "Familial immunoglobulin A nephropathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Familial immunoglobulin A nephropathy", "shortest_name_length": 24}
{"curie": "MONDO:0011503", "names": ["CORTRD1", "CORTISONE REDUCTASE DEFICIENCY 1", "cortisone reductase deficiency 1", "H6PD cortisone reductase deficiency", "Cortisone Reductase Deficiency Type 1", "cortisone reductase deficiency type 1", "apparent cortisone reductase deficiency", "hexose-6-phosphate dehydrogenase deficiency", "Hexose-6-Phosphate Dehydrogenase Deficiency", "Hexose-6-phosphate Dehydrogenase Deficiency", "cortisone reductase deficiency caused by mutation in H6PD"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cortisone reductase deficiency 1", "shortest_name_length": 7}
{"curie": "MONDO:0019170", "names": ["PAN", "Systemic PAN", "polyarteritis", "periarteritis", "kussmaul disease", "KUSSMAUL DISEASE", "disease; Kussmaul", "Kussmaul; disease", "Kussmaul's disease", "Panarteritis nodosa", "Panarteritis Nodosa", "PANARTERITIS NODOSA", "panarteritis nodosa", "nodosa polyarteritis", "Periarteritis Nodosa", "POLYARTERITIS NODOSA", "periarteritis nodosa", "Periarteritis nodosa", "PERIARTERITIS NODOSA", "polyarteritis nodosa", "Polyarteritis Nodosa", "Polyarteritis nodosa", "polyarteritis nodosum", "Polyarteritis nodosum", "Küssmaul-Maier disease", "PAN - Polyarteritis nodosa", "Classic polyarteritis nodosa", "classic polyarteritis nodosa", "Classic Polyarteritis Nodosa", "POLYARTERITIS NODOSA SYSTEMIC", "Systemic periarteritis nodosa", "Systemic polyarteritis nodosa", "Classical polyarteritis nodosa", "Classical Polyarteritis Nodosa", "classical polyarteritis nodosa", "Periarteritis nodosa, systemic", "Polyarteritis nodosa (disorder)", "panarteritis nodosa (diagnosis)", "periarteritis nodosa (diagnosis)", "polyarteritis nodosa (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyarteritis nodosa", "shortest_name_length": 3}
{"curie": "MONDO:0000440", "names": ["Acidosis", "Metabolic acidosis", "metabolic acidosis", "acidosis metabolic", "METABOLIC ACIDOSIS", "Metabolic Acidoses", "Acidosis metabolic", "ACIDOSIS METABOLIC", "Metabolic Acidosis", "Acidosis, metabolic", "Acidosis, Metabolic", "Acidoses, Metabolic", "metabolic; acidosis", "acidosis; metabolic", "Metabolic acidosis NOS", "Metabolic acidosis, NOS", "metabolic acidosis disorder", "Metabolic acidosis (disorder)", "metabolic acidosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metabolic acidosis", "shortest_name_length": 8}
{"curie": "MONDO:0700191", "names": ["chicken fibrosarcoma", "Chicken Fibrosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chicken fibrosarcoma", "shortest_name_length": 20}
{"curie": "UMLS:C0339933", "names": ["acute bronchitis bacterial", "acute bacterial bronchitis", "Acute bacterial bronchitis", "Acute bacterial bronchitis (disorder)", "acute bacterial bronchitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute bacterial bronchitis", "shortest_name_length": 26}
{"curie": "MONDO:0020333", "names": ["ASM", "Advanced Systemic Mastocytosis", "Aggressive Systemic Mastocytosis", "Aggressive systemic mastocytosis", "Aggressive Systemic Mastocytoses", "aggressive systemic mastocytosis", "Mastocytoses, Aggressive Systemic", "Systemic Mastocytoses, Aggressive", "Mastocytosis, Aggressive Systemic", "Systemic Mastocytosis, Aggressive", "Aggressive systemic mastocytosis (disorder)", "Aggressive systemic mastocytosis (diagnosis)", "lymphadenopathic mastocytosis with eosinophilia", "Lymphadenopathic mastocytosis with eosinophilia", "aggressive systemic mastocytosis (morphologic abnormality)", "aggressive lymphadenopathic mastocytosis with eosinophilia", "Aggressive systemic mastocytosis (morphologic abnormality)", "Aggressive lymphadenopathic mastocytosis with eosinophilia", "malignant mast cell tumor aggressive systemic mastocytosis", "Aggressive lymphadenopathic mastocytosis with eosinophilia (disorder)", "aggressive lymphadenopathic mastocytosis with eosinophilia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aggressive systemic mastocytosis", "shortest_name_length": 3}
{"curie": "UMLS:C3496549", "names": ["Male Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Male Germ Cell Tumor", "shortest_name_length": 20}
{"curie": "MONDO:0010734", "names": ["VSPA", "VISUOSPATIAL/PERCEPTUAL ABILITIES", "visuospatial/perceptual abilities", "SPATIAL VISUALIZATION, APTITUDE FOR", "spatial visualization, aptitude for", "Turner syndrome-associated Neurocognitive phenotype", "Turner Syndrome-Associated Neurocognitive Phenotype", "TURNER SYNDROME-ASSOCIATED NEUROCOGNITIVE PHENOTYPE", "visuospatial/perceptual abilities, X-linked recessive", "Turner syndrome-associated neurocognitive phenotype, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spatial visualization, aptitude for", "shortest_name_length": 4}
{"curie": "UMLS:C2987466", "names": ["Stage IV Sinonasal Cancer AJCC v6", "Stage IV Sinonasal Carcinoma AJCC v6", "Stage IV Nasal Cavity and Paranasal Sinus Cancer", "Stage IV Nasal Cavity and Paranasal Sinus Cancer AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Nasal Cavity and Paranasal Sinus Cancer AJCC v6", "shortest_name_length": 33}
{"curie": "MONDO:0056817", "names": ["Rectal Adenosquamous Cancer", "rectal adenosquamous cancer", "rectal adenosquamous carcinoma", "Rectal Adenosquamous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rectal adenosquamous carcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0010139", "names": ["CHNG4", "tsh deficiency", "TSH deficiency", "TSH Deficiency", "TSH DEFICIENCY", "Deficiency, TSH", "TSH Deficiencies", "Pituitary myxedema", "pituitary myxedema", "pituitary cretinism", "Pituitary cretinism", "PITUITARY CRETINISM", "Thyrotropin deficiency", "Isolated TSH deficiency", "isolated TSH deficiency", "Thyrotrophin deficiency", "secondary hypothyroidism", "PITUITARY HYPOTHYROIDISM", "hypothyroidism pituitary", "Pituitary Hypothyroidism", "Secondary hypothyroidism", "pituitary hypothyroidism", "Pituitary hypothyroidism", "hypothyroidism secondary", "Hypothyroidism, secondary", "TSH deficient hypothyroidism", "Hypothyrotropic hypothyroidism", "Isolated thyrotropin deficiency", "isolated thyrotropin deficiency", "THYROTROPIN DEFICIENCY, ISOLATED", "thyrotropin deficiency, isolated", "Thyrotropin deficiency, isolated", "Central congenital hypothyroidism", "thyrotropin, biologically inactive", "Thyrotropin, Biologically Inactive", "THYROTROPIN, BIOLOGICALLY INACTIVE", "Secondary hypothyroidism (disorder)", "secondary hypothyroidism (diagnosis)", "Congenital Nongoitrous Hypothyroidism", "thyroid-stimulating hormone deficiency", "THYROID-STIMULATING HORMONE DEFICIENCY", "Thyroid stimulating hormone deficiency", "Thyroid-stimulating hormone deficiency", "Thyroid-Stimulating Hormone Deficiency", "Thyroid Stimulating Hormone Deficiency", "Deficiency, Thyroid-Stimulating Hormone", "congenital nongoitrous hypothryoidism 4", "Hormone Deficiency, Thyroid-Stimulating", "congenital nongoitrous hypothyroidism 4", "Isolated thyrotropic hormone deficiency", "Thyroid-Stimulating Hormone Deficiencies", "hypothyroidism, congenital, nongoitrous 4", "hypothyroidism, congenital, nongoitrous, 4", "thyroid-stimulating hormone, deficiency of", "Hypothyroidism, Congenital, Nongoitrous, 4", "HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 4", "Isolated thyrotropin deficiency (disorder)", "TSH - Thyroid stimulating hormone deficiency", "Thyroid-stimulating hormone (TSH) deficiency", "isolated thyroid-stimulating hormone deficiency", "hypothyroidism, congenital, nongoitrous, type 4", "Isolated thyroid-stimulating hormone deficiency", "Low thyroid gland function due to abnormal pituitary gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated thyroid-stimulating hormone deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0018855", "names": ["KPA", "keratosis pilaris", "honeycomb atrophy", "Honeycomb atrophy", "Ulerythema of eyebrows", "ulerythema ophryogenes", "Ulerythema ophyrogenes", "ophryogenes ulerythema", "Ulerythema ophryogenes", "ophryogenes; ulerythema", "ulerythema; ophryogenes", "Ulerythema ophryogenesis", "Atrophodermia reticulata", "Vermiculata atrophoderma", "ulerythema ophryogenesis", "Atrophodermia vermiculata", "folliculitis ulerythematosa", "Folliculitis ulerythematosa", "KERATOSIS PILARIS ATROPHICANS", "keratosis pilaris atrophicans", "Keratosis pilaris atrophicans", "Ulerythema ophryogenes (disorder)", "Burnett Schwartz Berberian syndrome", "burnett Schwartz Berberian syndrome", "Keratosis pilaris atrophicans faciei", "keratosis pilaris atrophicans facies", "Keratosis Pilaris Atrophicans Facies", "folliculitis ulerythematosa reticulata", "Keratosis pilaris atrophicans (disorder)", "Atrophodermia reticulata symmetrica faciei", "ulerythema ophryogenes with multiple congenital anomalies", "Ulerythema ophryogenes with multiple congenital anomalies", "amelogenesis imperfecta, hypoplastic-hypomaturation, X-linked 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratosis pilaris atrophicans", "shortest_name_length": 3}
{"curie": "MONDO:0012061", "names": ["SSS1", "SICK SINUS SYNDROME 1", "familial sick sinus syndrome", "Familial sick sinus syndrome", "hereditary sick sinus syndrome", "SICK SINUS SYNDROME, CONGENITAL", "Sick Sinus Syndrome, Congenital", "familial sinus node dysfunction", "Sinus Rhythm, Congenital Absence of", "SINUS RHYTHM, CONGENITAL ABSENCE OF", "SINUS BRADYCARDIA SYNDROME, FAMILIAL", "Sinus Bradycardia Syndrome, Familial", "Familial sick sinus syndrome (disorder)", "SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE", "sick sinus syndrome 1, autosomal recessive", "Sick Sinus Syndrome 1, Autosomal Recessive", "Sinus Node Disease, Familial, Autosomal Recessive", "SINUS NODE DISEASE, FAMILIAL, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial sick sinus syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0100263", "names": ["PEX6 related Zellweger spectrum disorder", "peroxisome biogenesis disorder due to PEX6 defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder due to PEX6 defect", "shortest_name_length": 40}
{"curie": "UMLS:C0041912", "names": ["uri", "URI", "Cold", "URTI", "U.R.I.", "upper resp tract infection", "UPPER RESP TRACT INFECTION", "Infection;upper resp tract", "Respiratory Tract Infection", "Upper Respiratory Infection", "upper respiratory infection", "INFECTION UPPER RESPIRATORY", "Upper respiratory infection", "Infection upper respiratory", "UPPER RESPIRATORY INFECTION", "Respiratory Infection, Upper", "upper respiratory infections", "Upper Respiratory Infections", "Infections, Upper Respiratory", "Upper respiratory infection NOS", "Upper respiratory infection, NOS", "Upper respiratory tract infection", "RESPIRATORY TRACT INFECTION UPPER", "upper respiratory infection (URI)", "Upper Respiratory Tract Infection", "URI - Upper respiratory infection", "URI (upper respiratory infection)", "Upper respiratory tract infections", "Upper Respiratory Tract Infections", "Infections, Upper Respiratory Tract", "Upper Respiratory Tract Inflammation", "Upper respiratory tract infection NOS", "Upper respiratory infection (disorder)", "upper respiratory infection (diagnosis)", "upper respiratory tract infection (URTI)", "URTI (upper respiratory tract infection)", "Infection of the upper respiratory tract", "Upper respiratory tract infectious disease", "URTI - Infection of the upper respiratory tract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Upper Respiratory Infections", "shortest_name_length": 3}
{"curie": "MONDO:0025449", "names": ["Johne disease", "Johne Disease", "disease, Johne", "Disease, Johne", "Johnes disease", "Johnes Disease", "johnes disease", "johne's disease", "Johne's disease", "Johne's Disease", "paratuberculosis", "disease, Johne's", "Disease, Johne's", "Paratuberculosis", "Paratuberculoses", "Johne's disease (disorder)", "Infection due to Mycobacterium paratuberculosis", "Infection caused by Mycobacterium paratuberculosis", "Infection caused by Mycobacterium paratuberculosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paratuberculosis", "shortest_name_length": 13}
{"curie": "MONDO:0015430", "names": ["R1", "Ring 1", "r(1) syndrome", "chromosome 1 ring", "Ring Chromosome 1", "ring chromosome 1", "Chromosome 1 ring", "Ring chromosome 1", "chromosome 1, ring", "Ring chromosome type 1", "Ring chromosome 1 syndrome", "Ring chromosome 1 syndrome (disorder)", "Ring chromosome 1 syndrome (diagnosis)", "anomaly of chromosome pair ring 1 syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ring chromosome 1", "shortest_name_length": 2}
{"curie": "UMLS:C4682865", "names": ["Metastatic Nonfunctional Neuroendocrine Tumor", "Metastatic Non-Functioning Neuroendocrine Tumor", "Metastatic Nonfunctional Well Differentiated Neuroendocrine Tumor", "Metastatic Nonfunctional Well Differentiated Neuroendocrine Neoplasm", "Metastatic Nonfunctioning Well Differentiated Neuroendocrine Neoplasm", "Metastatic Non-Functioning Well Differentiated Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Non-Functioning Neuroendocrine Tumor", "shortest_name_length": 45}
{"curie": "MONDO:0014068", "names": ["CORD17", "CONE-ROD DYSTROPHY 17", "cone-rod dystrophy 17", "cone-rod dystrophy type 17"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cone-rod dystrophy 17", "shortest_name_length": 6}
{"curie": "UMLS:C0160692", "names": ["SVC injury", "Superior vena cava injury", "VENA CAVA SUPERIOR INJURY", "Injury to superior vena cava", "Injury of superior vena cava", "Injury to Superior Vena Cava", "injury of superior vena cava", "injury; vena cava (superior)", "v.cava; injury (superior vena cava)", "Injury of superior vena cava (disorder)", "injury of superior vena cava (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury to Superior Vena Cava", "shortest_name_length": 10}
{"curie": "MONDO:0000583", "names": ["IgB Deficiency", "IgB deficiency", "CD79B Deficiency", "immunoglobulin beta deficiency", "Immunodeficiency, Hypogammaglobulinemia, and Reduced B Cells"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunoglobulin beta deficiency", "shortest_name_length": 14}
{"curie": "MONDO:0010427", "names": ["MRXSR", "mental retardation, X-linked syndromic, Raymond type", "MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE", "mental retardation, X-linked, syndromic, Raymond type", "syndromic X-linked intellectual disability Raymond type", "intellectual disability, X-linked syndromic, Raymond type", "intellectual disability, X-linked, syndromic, Raymond type", "X-linked syndromic intellectual developmental disorder Raymond type", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, RAYMOND TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic X-linked intellectual disability Raymond type", "shortest_name_length": 5}
{"curie": "UMLS:C1840334", "names": ["Autosomal Recessive Hypoparathyroidism", "Hypoparathyroidism, Autosomal Recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypoparathyroidism, Autosomal Recessive", "shortest_name_length": 38}
{"curie": "UMLS:C5205060", "names": ["Refractory High Grade B-Cell Lymphoma", "Refractory High-Grade B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory High Grade B-Cell Lymphoma", "shortest_name_length": 37}
{"curie": "MONDO:0024316", "names": ["physiological malfunction arising from mental factor", "Physiological Malfunction Arising from Mental Factor", "physiological malfunction arising from mental Factor", "physiological malfunction arising from mental factors", "Physiological malfunction arising from mental factors"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "physiological malfunction arising from mental factor", "shortest_name_length": 52}
{"curie": "UMLS:C0854943", "names": ["Stage III Ovarian Choriocarcinoma", "Stage III Ovarian Choriocarcinoma AJCC v7", "Stage III Ovarian Choriocarcinoma AJCC v6", "Stage III Ovarian Germ Cell Choriocarcinoma", "Ovarian Germ Cell Choriocarcinoma Stage III", "Ovarian germ cell choriocarcinoma stage III", "Ovarian Germ Cell Choriocarcinoma, Stage III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian germ cell choriocarcinoma stage III", "shortest_name_length": 33}
{"curie": "MONDO:0011400", "names": ["CMD1G", "Dilated Cardiomyopathy-1G", "dilated cardiomyopathy 1G", "CARDIOMYOPATHY, DILATED, 1G", "cardiomyopathy, dilated, 1G", "Cardiomyopathy, Dilated, 1g", "dilated cardiomyopathy type 1G", "cardiomyopathy, dilated, type 1G", "TTN familial isolated dilated cardiomyopathy", "familial isolated dilated cardiomyopathy caused by mutation in TTN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1G", "shortest_name_length": 5}
{"curie": "UMLS:C0016664", "names": ["FOOT, MARCH", "March fracture", "March Fracture", "march fracture", "FRACTURE, MARCH", "STRESS FRACTURE", "March Fractures", "Stress Fracture", "march fractures", "Fracture;stress", "Stress fracture", "Stress reaction", "stress fracture", "Fracture, March", "stress; fracture", "fracture; stress", "stress fractures", "FATIGUE FRACTURE", "fatigue fracture", "Fractures, March", "Fracture, Stress", "Stress Fractures", "Fatigue Fracture", "Fatigue fracture", "Fracture, Fatigue", "Fatigue fractures", "fracture; fatigue", "Fatigue Fractures", "fatigue; fracture", "Fractures, Stress", "Fractures, Fatigue", "Capillary fracture", "[Q] Stress fracture", "Stress fracture NOS", "march fracture; fracture", "fracture; march fracture", "March fracture (disorder)", "Stress fracture (disorder)", "March fracture (diagnosis)", "stress fracture (diagnosis)", "Stress fracture (morphologic abnormality)", "fracture of metatarsal bone(s) march fracture"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stress Fractures", "shortest_name_length": 11}
{"curie": "UMLS:C2987478", "names": ["Stage III Vulvar Cancer", "Stage III Vulvar Carcinoma", "Stage III Vulvar Cancer AJCC v7", "Stage III Vulvar Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Vulvar Cancer AJCC v7", "shortest_name_length": 23}
{"curie": "MONDO:0002081", "names": ["Orthopedic Disorder", "Orthopedic Disorders", "disease musculoskeletal", "MUSCULOSKELETAL DISEASE", "musculoskeletal disease", "Musculoskeletal Disease", "Musculoskeletal disease", "Disease;musculoskeletal", "musculoskeletal disorder", "disorder musculoskeletal", "Musculoskeletal Diseases", "Musculoskeletal Disorder", "diseases musculoskeletal", "musculoskeletal diseases", "Musculoskeletal disorder", "Skeletomuscular Disorders", "musculoskeletal disorders", "Musculoskeletal Disorders", "disorders musculoskeletal", "disorders musculo skeletal", "Musculoskeletal disorder NOS", "musculoskeletal system disease", "disease musculoskeletal system", "Musculoskeletal System Disorder", "musculoskeletal system disorder", "diseases musculoskeletal system", "disorders musculoskeletal system", "Musculoskeletal system--Diseases", "MUSCULO-SKELETAL SYSTEM DISORDERS", "disease of musculoskeletal system", "Disorder of Musculoskeletal System", "disorder of musculoskeletal system", "Disorder of musculoskeletal system", "musculoskeletal system disease or disorder", "musculoskeletal system disease (diagnosis)", "Disease of the musculoskeletal system, NOS", "Disorder of the musculoskeletal system, NOS", "Disorder of musculoskeletal system (disorder)", "disease or disorder of musculoskeletal system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "musculoskeletal system disorder", "shortest_name_length": 19}
{"curie": "UMLS:C0343466", "names": ["Type 2 lepra reaction", "Erythema nodosum leprosum", "Immune complex reaction co-occurrent and due to multibacillary leprosy", "Immune complex reaction co-occurrent and due to multibacillary leprosy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Type 2 lepra reaction", "shortest_name_length": 21}
{"curie": "MONDO:0020532", "names": ["Sodoku", "SODOKU", "sodoku", "Sokosho", "Sokosha", "Spirillosis", "spirillosis", "sodoku disease", "Spirillary fever", "spirillary fever", "spirillary; fever", "fever; spirillary", "Spirillary rat-bite fever", "Rat-bite spirillary fever", "spirillary rat-bite fever", "RAT-BITE FEVER, SPIRILLARY", "Spirillary fever (disorder)", "SPIRILLUM MINUS RAT BITE FEVER", "Spirillum minus rat bite fever", "Rat-bite fever due to S. minus", "Spirillum minus rat-bite fever", "rat-bite fever Spirillum minus", "Spirillum minor rat-bite fever", "Spirillum minor rat bite fever", "SPIRILLUM MINUS <RAT BITE FEVER>", "fever; rat-bite, due to Spirillum", "rat-bite; fever, due to Spirillum", "Rat-bite fever due to Spirillum minus", "rat-bite fever due to Spirillum minus", "Rat-bite fever due to Spirillum minor", "rat-bite fever due to Spirillum minus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spirillary rat-bite fever", "shortest_name_length": 6}
{"curie": "MONDO:0024502", "names": ["gall bladder NET", "Gallbladder neuroendocrine tumor", "Gallbladder neuroendocrine tumour", "gall bladder neuroendocrine tumor", "Gallbladder Neuroendocrine Neoplasm", "gallbladder neuroendocrine neoplasm", "gall bladder neuroendocrine neoplasm", "Neuroendocrine neoplasm of gallbladder", "neuroendocrine neoplasm of gall bladder", "Neuroendocrine neoplasm of gallbladder (disorder)", "gall bladder neuroendocrine tumor, well differentiated, low or intermediate grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gallbladder neuroendocrine neoplasm", "shortest_name_length": 16}
{"curie": "MONDO:0012090", "names": ["DFNA47", "autosomal dominant deafness 47", "Deafness, Autosomal Dominant 47", "DEAFNESS, AUTOSOMAL DOMINANT 47", "deafness, autosomal dominant 47", "autosomal dominant nonsyndromic deafness 47", "autosomal dominant nonsyndromic hearing loss 47", "autosomal dominant nonsyndromic deafness type 47"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 47", "shortest_name_length": 6}
{"curie": "UMLS:C1336341", "names": ["Stage IVA Hypopharynx Epidermoid Carcinoma", "Stage IVA Hypopharynx Squamous Cell Carcinoma", "Stage IVA Hypopharyngeal Epidermoid Carcinoma", "Stage IVA Epidermoid Carcinoma of Hypopharynx", "Stage IVA Squamous Cell Carcinoma of Hypopharynx", "Stage IVA Hypopharyngeal Squamous Cell Carcinoma", "Stage IVA Epidermoid Carcinoma of the Hypopharynx", "Stage IVA Hypopharyngeal Throat Squamous Cell Cancer", "Stage IVA Squamous Cell Carcinoma of the Hypopharynx", "Stage IVA Hypopharyngeal Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Hypopharyngeal Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 42}
{"curie": "UMLS:C2930843", "names": ["Idiopathic intracranial hypertension with papilledema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Idiopathic intracranial hypertension with papilledema", "shortest_name_length": 53}
{"curie": "UMLS:C5420409", "names": ["Bithalamic Glioma", "Bilateral Thalamic Glioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bilateral Thalamic Glioma", "shortest_name_length": 17}
{"curie": "MONDO:0010755", "names": ["VURX", "VESICOURETERAL REFLUX, X-LINKED", "vesicoureteral reflux, X-linked", "Vesicoureteral Reflux, X-Linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vesicoureteral reflux, X-linked", "shortest_name_length": 4}
{"curie": "MONDO:0001801", "names": ["staphyloma posticum", "Staphyloma posticum", "Posterior staphyloma", "Partial scleral ectasia", "Posterior scleral staphyloma", "Staphyloma posticum (disorder)", "staphyloma posticum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "staphyloma posticum", "shortest_name_length": 19}
{"curie": "UMLS:C0269388", "names": ["Miscarriage in first trimester", "1st Trimester Spontaneous Abortion", "ABORTION SPONTANEOUS FIRST TRIMESTER", "First Trimester Spontaneous Abortion", "spontaneous abortion in first trimester", "Spontaneous abortion in first trimester", "Miscarriage in first trimester (disorder)", "spontaneous abortion in first trimester (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Miscarriage in first trimester", "shortest_name_length": 30}
{"curie": "MONDO:0003709", "names": ["AGORAPHOBIA", "agoraphobia", "Agoraphobia", "agoraphobias", "Agoraphobias", "Crowds Phobia", "Phobia, Crowds", "fear open spaces", "Agoraphobia, NOS", "Open Spaces Phobia", "Phobia, Open Spaces", "fear of open spaces", "Fear of open spaces", "Fear of open places", "Phobia of going out", "Agoraphobia (disorder)", "agoraphobia (diagnosis)", "Agoraphobia, unspecified", "Fear of open spaces (finding)", "fear of open spaces (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "agoraphobia", "shortest_name_length": 11}
{"curie": "MONDO:0020146", "names": ["major induction processes eye anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "major induction processes eye anomaly", "shortest_name_length": 37}
{"curie": "UMLS:C4526858", "names": ["Recurrent Cervical Adenosquamous Cancer", "Relapsed Cervical Adenosquamous Carcinoma", "Recurrent Cervical Adenosquamous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Cervical Adenosquamous Carcinoma", "shortest_name_length": 39}
{"curie": "UMLS:C0686637", "names": ["Secondary malignant neoplasm of supraclavicular lymph nodes", "Metastatic malignant neoplasm of supraclavicular lymph nodes", "Metastatic malignant neoplasm to supraclavicular lymph nodes", "lymph node neoplasm malignant secondary neck supraclavicular", "metastasis of malignant neoplasm to supraclavicular lymph nodes", "malignant neoplasm metastasis to the supraclavicular lymph nodes", "Metastatic Malignant Neoplasm in the Supraclavicular Lymph Nodes", "Metastatic malignant neoplasm to supraclavicular lymph nodes (disorder)", "Secondary malignant neoplasm of supraclavicular lymph nodes (diagnosis)", "metastasis of malignant neoplasm to supraclavicular lymph nodes (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to supraclavicular lymph nodes", "shortest_name_length": 59}
{"curie": "UMLS:C0588006", "names": ["mild depression", "Mild depression", "depression mild", "Depression, mild", "Mild depression (disorder)", "Mild depression (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mild depression", "shortest_name_length": 15}
{"curie": "MONDO:0026730", "names": ["MRXSBA", "MRXS36", "Basilicata-Akhtar syndrome", "BASILICATA-AKHTAR SYNDROME", "X-linked syndromic mental retardation 36", "MENTAL RETARDATION, X-LINKED, SYNDROMIC 36", "Mental Retardation, X-Linked, Syndromic 36", "Basilicata-Akhtar syndrome, X-linked dominant", "X-linked syndromic mental retardation Basilicata-Akhtar type", "MENTAL RETARDATION, X-LINKED, SYNDROMIC, BASILICATA-AKHTAR TYPE", "Mental Retardation, X-Linked, Syndromic, Basilicata-Akhtar Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Basilicata-Akhtar syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C5238468", "names": ["Locally Advanced Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Neuroendocrine Neoplasm", "shortest_name_length": 40}
{"curie": "UMLS:C5418826", "names": ["Unresectable Rhabdoid Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Rhabdoid Tumor", "shortest_name_length": 27}
{"curie": "UMLS:C1096668", "names": ["Instillation site irritation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Instillation site irritation", "shortest_name_length": 28}
{"curie": "MONDO:0013094", "names": ["GLM5", "GLIOMA SUSCEPTIBILITY 5", "glioma susceptibility 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glioma susceptibility 5", "shortest_name_length": 4}
{"curie": "UMLS:C0238421", "names": ["low ses", "Se++ low", "Se levels low", "SELENIUM DEFICIENCY", "selenium deficiency", "Selenium deficiency", "deficiency selenium", "deficiency; selenium", "selenium; deficiency", "Selenium deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Selenium deficiency", "shortest_name_length": 7}
{"curie": "MONDO:0030977", "names": ["HMNMYO", "NEUROPATHY, HEREDITARY MOTOR, WITH MYOPATHIC FEATURES", "neuropathy, hereditary motor, with myopathic features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuropathy, hereditary motor, with myopathic features", "shortest_name_length": 6}
{"curie": "UMLS:C1698511", "names": ["anastomotic leak rectum", "Rectal anastomotic leak", "Rectal Anastomotic Leakage", "Rectal anastomotic leak (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rectal Anastomotic Leakage", "shortest_name_length": 23}
{"curie": "UMLS:C0278773", "names": ["Unresectable Liver Cancer", "Localized Non-Resectable Adult Liver Cancer", "Localized Unresectable Adult Liver Carcinoma", "Localized Non-Resectable Adult Liver Carcinoma", "localized unresectable adult primary liver cancer", "Localized Unresectable Adult Primary Liver Cancer", "adult primary liver cancer, localized unresectable", "liver cancer, localized unresectable adult primary", "Localized Unresectable Adult Primary Cancer of Liver", "Localized Unresectable Adult Primary Cancer of the Liver"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized Non-Resectable Adult Liver Carcinoma", "shortest_name_length": 25}
{"curie": "UMLS:C0017107", "names": ["gas poison", "Gas poisoning", "Gas Poisoning", "gas poisoning", "poisoning gas", "Poisoning, Gas", "Gas Poisonings", "gas; poisoning", "poisoning; gas", "Poisonings, Gas", "Gas poisoning, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gas Poisoning", "shortest_name_length": 10}
{"curie": "MONDO:0005787", "names": ["liver tuberculosis", "tuberculosis liver", "Tuberculosis liver", "hepatic tuberculosis", "Hepatic Tuberculoses", "Hepatic Tuberculosis", "Tuberculosis, Hepatic", "Tuberculoses, Hepatic", "Tuberculosis of liver", "tuberculosis of liver", "Tuberculosis of liver (disorder)", "tuberculosis of liver (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatic tuberculosis", "shortest_name_length": 18}
{"curie": "MONDO:0018037", "names": ["HIES", "Hyper IgE", "hyper IgE syndrome", "hyper-IgE syndrome", "hyperimmunoglobulin E syndrome", "Hyperimmunoglobulin E Syndrome", "hyper immunoglobulin E syndrome", "hyper-IgE recurrent infection syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyper-IgE syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0022849", "names": ["congenital stenosis of cervical medullary canal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital stenosis of cervical medullary canal", "shortest_name_length": 47}
{"curie": "MONDO:0019127", "names": ["PM", "POLYMYOSITIS", "Polymyositis", "polymyositis", "Neuromyositis", "Polymyositides", "PM - Polymyositis", "multiple myositis", "Multiple Myositis", "Myositis, Multiple", "Myositides, Multiple", "Polymyositis (disorder)", "polymyositis (diagnosis)", "Clinical polymyositis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polymyositis", "shortest_name_length": 2}
{"curie": "MONDO:0021276", "names": ["buccal mucosa papilloma", "Buccal Mucosa Papilloma", "Buccal Squamous Papilloma", "Papilloma of buccal mucosa", "Papilloma of Buccal Mucosa", "papilloma of buccal mucosa", "Buccal Squamous Cell Papilloma", "Papilloma of the Buccal Mucosa", "papilloma of the buccal mucosa", "Papilloma of buccal mucosa (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papilloma of buccal mucosa", "shortest_name_length": 23}
{"curie": "MONDO:0030840", "names": ["MMRCS2", "mismatch repair cancer syndrome 2", "MISMATCH REPAIR CANCER SYNDROME 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mismatch repair cancer syndrome 2", "shortest_name_length": 6}
{"curie": "MONDO:0019731", "names": ["AApoAI amyloidosis", "apolipoprotein A-I amyloidosis", "familial renal amyloidosis due to apolipoprotein A-I variant", "familial amyloid nephropathy due to apolipoprotein A-I variant", "hereditary renal amyloidosis due to apolipoprotein A-I variant", "hereditary amyloid nephropathy due to apolipoprotein A-I variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AApoAI amyloidosis", "shortest_name_length": 18}
{"curie": "MONDO:0021190", "names": ["DNA repair disease", "DNA repair disorder", "DNA Repair Disorder", "Deficient DNA Repair", "deficient DNA repair", "Repair, Deficient DNA", "repair, deficient DNA", "deficient DNA Repairs", "DNA Repair-Deficiency", "Deficient DNA Repairs", "DNA Repair, Deficient", "DNA repair deficiency", "DNA repair-deficiency", "DNA repair, deficient", "DNA Repair Deficiency", "Repairs, Deficient DNA", "disorder of DNA repair", "DNA Repairs, Deficient", "DNA Repairs, deficient", "Repairs, deficient DNA", "DNA repair-deficiencies", "DNA Repair-Deficiencies", "Deficiency of DNA repair", "deficiency of DNA repair", "Deficiency of DNA repair, NOS", "DNA repair-deficiency disorder", "DNA Repair-Deficiency Disorder", "chromosome instability syndrome", "DNA repair deficiency disorders", "disorder, DNA repair-deficiency", "DNA Repair-Deficiency Disorders", "Disorder, DNA Repair-Deficiency", "DNA Repair Deficiency Disorders", "syndrome, chromosome instability", "Disorders, DNA Repair-Deficiency", "disorders, DNA repair-deficiency", "chromosome instability syndromes", "syndromes, chromosome instability", "Deficiency of deoxyribonucleic acid repair", "Deficiency of deoxyribonucleic acid repair (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DNA repair disease", "shortest_name_length": 18}
{"curie": "MONDO:0015265", "names": ["BO", "BOOP", "organized pneumonia", "organizing pneumonia", "bronchiolitis exudativa", "Bronchiolitis exudativa", "Bronchiolitis Obliterans", "bronchiolitis obliterans", "BRONCHIOLITIS OBLITERANS", "Bronchiolitis obliterans", "Obliterative bronchiolitis", "bronchiolitis obliterative", "OBLITERATIVE BRONCHIOLITIS", "Constrictive bronchiolitis", "Constrictive Bronchiolitis", "obliterative bronchiolitis", "constrictive bronchiolitis", "obliterative; bronchiolitis", "bronchiolitis; obliterative", "Bronchiolitis, Constrictive", "Constrictive Bronchiolitides", "Bronchiolitides, Constrictive", "Obliterative bronchiolitis, NOS", "OB - Obliterative bronchiolitis", "bronchiolitis fibrosa obliterans", "Bronchiolitis fibrosa obliterans", "bronchiolitis; fibrosa obliterans", "bronchiolitis obliterans syndrome", "fibrosa obliterans; bronchiolitis", "bronchiolitis obliterans (diagnosis)", "Obliterative bronchiolitis (disorder)", "obliterative bronchiolitis (diagnosis)", "bronchiolitis obliterans with obstructive pulmonary disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bronchiolitis obliterans syndrome", "shortest_name_length": 2}
{"curie": "UMLS:C4683635", "names": ["Mixed Cellularity Classic Hodgkin Lymphoma by Ann Arbor Stage", "Mixed Cellularity Classical Hodgkin Lymphoma by Ann Arbor Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mixed Cellularity Classic Hodgkin Lymphoma by Ann Arbor Stage", "shortest_name_length": 61}
{"curie": "OMIM:212540", "names": ["CAMAK Syndrome", "CAMAK SYNDROME", "CAMFAK syndrome", "CAMFAK SYNDROME", "Cataract-microcephaly-failure to thrive-kyphoscoliosis", "CATARACT, MICROCEPHALY, ARTHROGRYPOSIS, KYPHOSIS SYNDROME", "Cataract, Microcephaly, Arthrogryposis, Kyphosis Syndrome", "CATARACT, MICROCEPHALY, FAILURE TO THRIVE, KYPHOSCOLIOSIS SYNDROME", "Cataract, Microcephaly, Failure To Thrive, Kyphoscoliosis Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 14}
{"curie": "UMLS:C1708653", "names": ["Laryngeal Lymphoepithelioma", "Laryngeal Lymphoepithelial Carcinoma", "Laryngeal Undifferentiated Carcinoma of the Nasopharyngeal Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laryngeal Lymphoepithelial Carcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C0279645", "names": ["Acute Monoblastic Leukemia", "pediatric acute M5a leukemia", "childhood acute M5a leukemia", "Pediatric Acute M5a Leukemia", "Childhood Acute M5a Leukemia", "M5a leukemia, childhood acute", "Childhood Acute Monoblastic Leukemia", "pediatric acute monoblastic leukemia", "pediatric AMOL, poorly differentiated", "childhood AMOL, poorly differentiated", "monoblastic leukemia, childhood acute", "acute monoblastic leukemia, childhood", "leukemia, pediatric acute monoblastic", "childhood acute monoblastic leukemia (M5a)", "pediatric acute poorly differentiated monocytic leukemia", "childhood acute monocytic leukemia without differentiation", "pediatric acute monocytic leukemia without differentiation", "acute monocytic leukemia without differentiation, childhood", "leukemia, childhood acute monocytic without differentiation", "M5a childhood acute poorly differentiated monocytic leukemia", "Pediatric Acute Monoblastic Leukemia without Differentiation", "Childhood Acute Monoblastic Leukemia without Differentiation", "M5a childhood acute monocytic leukemia without differentiation", "M5a pediatric acute monocytic leukemia without differentiation", "childhood acute poorly differentiated monocytic leukemia (M5a)", "M5a Pediatric Acute Monoblastic Leukemia without Differentiation", "M5a Childhood Acute Monoblastic Leukemia without Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Acute Monoblastic Leukemia", "shortest_name_length": 26}
{"curie": "MONDO:0007102", "names": ["amyotrophic dystonic paraplegia", "Amyotrophic Dystonic Paraplegia", "AMYOTROPHIC DYSTONIC PARAPLEGIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyotrophic dystonic paraplegia", "shortest_name_length": 31}
{"curie": "MONDO:0054565", "names": ["SRTD17", "SHORT-RIB THORACIC DYSPLASIA 17 WITH OR WITHOUT POLYDACTYLY", "short-rib thoracic dysplasia 17 with or without POLYDACTYLY", "short-rib thoracic dysplasia 17 with or without polydactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short-rib thoracic dysplasia 17 with or without polydactyly", "shortest_name_length": 6}
{"curie": "UMLS:C2063737", "names": ["Pulmonary Artery Stenosis, Supravalvar", "supravalvular pulmonary artery stenosis", "Supravalvular Pulmonary Artery Stenosis", "stenosis of supravalvular pulmonary artery", "stenosis of supravalvular pulmonary artery (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stenosis of supravalvular pulmonary artery", "shortest_name_length": 38}
{"curie": "MONDO:0011514", "names": ["TRICUSPID ATRESIA", "Tricuspid atresia", "Tricuspid Atresia", "tricuspid atresia", "Tricuspid Atresias", "Atresia, Tricuspid", "Atresias, Tricuspid", "Tricuspid valve atresia", "Tricuspid Valve Atresia", "tricuspid valve atresia", "TRICUSPID VALVE, ATRESIA", "Tricuspid Valve Atresias", "Valve Atresia, Tricuspid", "atresia; tricuspid valve", "Atresia, Tricuspid Valve", "Valve Atresias, Tricuspid", "Atresias, Tricuspid Valve", "tricuspid (valve); atresia", "tricuspid atresia (disease)", "tricuspid atresia (diagnosis)", "Congenital tricuspid valve atresia", "right atrioventricular valve atresia", "Right atrioventricular valve atresia", "Congenital atresia of tricuspid valve", "Congenital Atresia of Tricuspid Valve", "congenital atresia of tricuspid valve", "Absent Right Atrioventricular Connection", "congenital agenesis of the tricuspid valve", "Right atrioventricular valve atresia (disorder)", "Congenital atresia of tricuspid valve (disorder)", "right atrioventricular valve atresia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tricuspid atresia", "shortest_name_length": 17}
{"curie": "MONDO:0001492", "names": ["kyphoscoliosis; heart", "heart; kyphoscoliosis", "Kyphoscoliotic heart disease", "kyphoscoliotic heart disease", "heart; disease, kyphoscoliotic", "Kyphoscoliotic heart disease (disorder)", "kyphoscoliotic heart disease (diagnosis)", "disease (or disorder); heart, kyphoscoliotic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kyphoscoliotic heart disease", "shortest_name_length": 21}
{"curie": "MONDO:0017225", "names": ["null syndrome", "PLP1 null syndrome", "Pelizaeus-Merzbacher disease, null syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "null syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0006795", "names": ["hypersplenia", "Hypersplenia", "Hypersplenism", "HYPERSPLENISM", "hypersplenism", "Hypersplenism, NOS", "Big spleen syndrome", "hyperfunction; spleen", "Hypersplenism syndrome", "hypersplenism (disease)", "Hypersplenism (disorder)", "hypersplenism (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypersplenism", "shortest_name_length": 12}
{"curie": "UMLS:C1336019", "names": ["Soft Palate Benign Granular Cell Tumor", "Soft Palate Benign Granular Cell Neoplasm", "Benign Granular Cell Tumor of Soft Palate", "Benign Granular Cell Neoplasm of Soft Palate", "Benign Granular Cell Tumor of the Soft Palate", "Benign Granular Cell Neoplasm of the Soft Palate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Soft Palate Benign Granular Cell Tumor", "shortest_name_length": 38}
{"curie": "UMLS:C3826981", "names": ["Pancreatic MD-IPMN", "Main Duct Pancreatic Intraductal Papillary-Mucinous Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Main Duct Pancreatic Intraductal Papillary-Mucinous Neoplasm", "shortest_name_length": 18}
{"curie": "MONDO:0020801", "names": ["rectal medullary carcinoma", "Rectal Medullary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rectal medullary carcinoma", "shortest_name_length": 26}
{"curie": "UMLS:C4288013", "names": ["AGMLGs", "Vulvar Adenocarcinoma of Mammary Gland Type", "Adenocarcinoma of Anogenital Mammary-Like Glands", "Adenocarcinoma of Anogenital Mammary-Type Glands", "Adenocarcinoma of the Vulva with Breast Carcinoma Features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Adenocarcinoma of Mammary Gland Type", "shortest_name_length": 6}
{"curie": "UMLS:C0282504", "names": ["Environmental Allergy", "Environmental Illness", "environmental illness", "Environmental allergy", "environmental allergy", "Illness, Environmental", "Environmental allergies", "environmental illnesses", "ENVIRONMENTAL ALLERGIES", "environmental allergies", "Environmental Illnesses", "Illnesses, Environmental", "Environmental Hypersensitivity", "Hypersensitivity, Environmental", "Environmental allergy (finding)", "Environmental Hypersensitivities", "Hypersensitivities, Environmental"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Environmental Illness", "shortest_name_length": 21}
{"curie": "UMLS:C2982916", "names": ["Stage II Lung Cancer", "Stage II Lung Cancer AJCC v6", "Stage II Lung Carcinoma AJCC v6", "Stage II Carcinoma of Lung AJCC v6", "Stage II Carcinoma of the Lung AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Lung Cancer AJCC v6", "shortest_name_length": 20}
{"curie": "UMLS:C0919947", "names": ["Thoracic vertebral fracture"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thoracic vertebral fracture", "shortest_name_length": 27}
{"curie": "MONDO:0015053", "names": ["HAE-I", "HAE 1", "hereditary angioedema type 1", "Hereditary angioedema - type 1", "Hereditary angio-edema - type 1", "Hereditary angio-oedema - type 1", "hereditary angioneurotic edema type 1", "Hereditary angioneurotic edema - type 1", "Hereditary angioneurotic oedema - type 1", "C1 esterase inhibitor deficiency - type 1", "c1 inhibitor deficiency - deficient factor", "hereditary C1 inhibitor deficiency - deficient factor", "Hereditary C1 esterase inhibitor deficiency - deficient factor", "hereditary C1 inhibitor deficiency - deficient factor (diagnosis)", "Hereditary C1 esterase inhibitor deficiency - deficient factor (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary angioedema type 1", "shortest_name_length": 5}
{"curie": "UMLS:C0393912", "names": ["Segmental autonomic dysfunction", "Segmental Autonomic Dysfunction", "Segmental Autonomic Dysfunctions", "Autonomic Dysfunction, Segmental", "Autonomic Dysfunctions, Segmental", "Segmental autonomic dysfunction (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Segmental Autonomic Dysfunction", "shortest_name_length": 31}
{"curie": "MONDO:0022749", "names": ["Non-neoplastic nevus", "non-neoplastic nevus", "Non-Neoplastic Nevus", "nevus; non-neoplastic", "Nevus, non-neoplastic", "Non-neoplastic naevus", "non-neoplastic; nevus", "Naevus, non-neoplastic", "Non-neoplastic nevus of skin", "Non-neoplastic naevus of skin", "Non-neoplastic nevus (disorder)", "non-neoplastic nevus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-neoplastic nevus", "shortest_name_length": 20}
{"curie": "MONDO:0014945", "names": ["MSP4", "DMRV", "MULTISYSTEM PROTEINOPATHY 4", "distal myopathy with rimmed vacuoles", "myopathy, distal, with rimmed vacuoles", "MYOPATHY, DISTAL, WITH RIMMED VACUOLES", "myopathy, distal, with rimmed vacuoles; DMRV"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy, distal, with rimmed vacuoles", "shortest_name_length": 4}
{"curie": "MONDO:0030453", "names": ["DEE97", "early infantile epileptic encephalopathy 97", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 97", "developmental and epileptic encephalopathy 97"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy 97", "shortest_name_length": 5}
{"curie": "UMLS:C0277964", "names": ["crepitus", "Crepitus", "Subcutaneous crepitus", "crepitus subcutaneous", "Subcutaneous crepitation", "Subcutaneous crepitus (finding)", "CREPITATION, SUBCUTANEOUS TISSUE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subcutaneous crepitus", "shortest_name_length": 8}
{"curie": "MONDO:0037821", "names": ["porphyrin metabolism disease", "disorder of porphyrin metabolism", "disorder of porphyrin and heme metabolism", "porphyrin-containing compound metabolic process disease", "disorder of porphyrin-containing compound metabolic process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "porphyrin metabolism disease", "shortest_name_length": 28}
{"curie": "UMLS:C4524745", "names": ["Postneoadjuvant Therapy Stage II Gastroesophageal Junction Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postneoadjuvant Therapy Stage II Gastroesophageal Junction Adenocarcinoma AJCC v8", "shortest_name_length": 81}
{"curie": "UMLS:C5669901", "names": ["Thalassemic Osteopathy", "Thalassemic Bone Disease", "Thalassemia Bone Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thalassemic Osteopathy", "shortest_name_length": 22}
{"curie": "MONDO:0002012", "names": ["Methymalonicaciduria", "methylmalonic aciduria", "Methylmalonic aciduria", "Methylmalonic Acidemia", "methylmalonic acidemia", "Methylmalonic Aciduria", "Methylmalonic acidemia", "MMA - Methylmalonic aciduria", "methylmalonic aciduria mut type", "methylmalonic aciduria type cblA", "methylmalonic aciduria type cblB", "methylmalonic aciduria, mut type", "methylmalonic aciduria cblB type", "methylmalonic acidemia, cblB type", "methylmalonic acidemia, cblA type", "methylmalonic aciduria (diagnosis)", "High blood methylmalonic acid levels", "METHYLMALONICACIDURIA due to methylmalonic CoA mutase deficiency", "methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency", "METHYLMALONICACIDURIA, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin--Cbl A", "METHYLMALONICACIDURIA, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin--Cbl B", "methylmalonic aciduria, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin, cblA type", "methylmalonic aciduria, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin, cblB type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "methylmalonic acidemia", "shortest_name_length": 20}
{"curie": "MONDO:0004475", "names": ["thymus clear cell carcinoma", "Thymic Clear Cell Carcinoma", "Thymus clear cell carcinoma", "Thymus Clear Cell Carcinoma", "thymic clear cell carcinoma", "clear cell carcinoma of Thymus", "Clear Cell Carcinoma of Thymus", "Clear Cell Carcinoma of the Thymus", "clear cell carcinoma of the Thymus", "Clear cell carcinoma of the Thymus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thymus clear cell carcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C0276357", "names": ["Swine influenza", "Swine Influenza", "swine influenza", "Influenza, Swine", "porcine influenza"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Swine influenza", "shortest_name_length": 15}
{"curie": "UMLS:C1336470", "names": ["Stage I Mouth Carcinoma", "Stage I Carcinoma of Mouth", "Stage I Oral Cavity Cancer", "Stage I Oral Cavity Carcinoma", "Stage I Carcinoma of the Mouth", "Stage I Carcinoma of Oral Cavity", "Stage I Oral Cavity Cancer AJCC v6", "Stage I Oral Cavity Cancer AJCC v7", "Stage I Carcinoma of the Oral Cavity", "Stage I Oral Cavity Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Oral Cavity Cancer AJCC v6 and v7", "shortest_name_length": 23}
{"curie": "UMLS:C1863769", "names": ["Dehydrated Hereditary Stomatocytosis, Pseudohyperkalemia, and Perinatal Edema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dehydrated Hereditary Stomatocytosis, Pseudohyperkalemia, and Perinatal Edema", "shortest_name_length": 77}
{"curie": "MONDO:0013157", "names": ["MDDGA5", "muscle-eye-brain-FKRP related", "congenital muscular dystrophy-dystroglycanopathy type A5", "Walker-Warburg syndrome or muscle-eye-brain disease, FKRP-related", "WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, FKRP-RELATED", "congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5", "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A5", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5", "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A5", "shortest_name_length": 6}
{"curie": "UMLS:C0338329", "names": ["Recurrent Brain Stem Glioma", "Relapsed Pediatric Brainstem Glioma", "Relapsed Childhood Brainstem Glioma", "Relapsed Pediatric Brain Stem Glioma", "Recurrent Pediatric Brainstem Glioma", "Recurrent Childhood Brainstem Glioma", "Relapsed Childhood Brain Stem Glioma", "glioma, recurrent pediatric brainstem", "recurrent childhood brain stem glioma", "Recurrent Pediatric Brain Stem Glioma", "glioma, recurrent childhood brainstem", "recurrent pediatric brain stem glioma", "Recurrent Childhood Brain Stem Glioma", "glioma, recurrent childhood brain stem", "childhood brain stem glioma, recurrent", "Relapsed Childhood Glioma of Brainstem", "brainstem glioma, pediatric, recurrent", "pediatric brain stem glioma, recurrent", "brainstem glioma, childhood, recurrent", "Relapsed Pediatric Glioma of Brainstem", "glioma, recurrent pediatric brain stem", "Recurrent Childhood Glioma of Brainstem", "brain stem glioma, childhood, recurrent", "Relapsed Childhood Glioma of Brain Stem", "Recurrent Pediatric Glioma of Brainstem", "brain stem glioma, pediatric, recurrent", "Relapsed Pediatric Glioma of Brain Stem", "Recurrent Pediatric Glioma of Brain Stem", "Recurrent Childhood Glioma of Brain Stem", "Relapsed Childhood Glioma of the Brainstem", "Relapsed Pediatric Glioma of the Brainstem", "gliosarcoma, recurrent childhood brainstem", "childhood brainstem gliosarcoma, recurrent", "pediatric brainstem gliosarcoma, recurrent", "Recurrent Childhood Glioma of the Brainstem", "mixed glioma, recurrent childhood brainstem", "Relapsed Childhood Glioma of the Brain Stem", "childhood brain stem gliosarcoma, recurrent", "childhood brainstem mixed glioma, recurrent", "gliosarcoma, recurrent childhood brain stem", "Relapsed Pediatric Glioma of the Brain Stem", "mixed glioma, recurrent pediatric brainstem", "pediatric brainstem mixed glioma, recurrent", "pediatric brain stem gliosarcoma, recurrent", "gliosarcoma, recurrent pediatric brain stem", "Recurrent Pediatric Glioma of the Brainstem", "pediatric brain stem mixed glioma, recurrent", "childhood brain stem mixed glioma, recurrent", "Recurrent Pediatric Glioma of the Brain Stem", "mixed glioma, recurrent pediatric brain stem", "Recurrent Childhood Glioma of the Brain Stem", "mixed glioma, recurrent childhood brain stem", "childhood CNS tumor, recurrent brainstem glioma", "pediatric CNS tumor, recurrent brainstem glioma", "CNS tumor, recurrent pediatric brainstem glioma", "CNS tumor, recurrent childhood brainstem glioma", "CNS tumor, recurrent pediatric brain stem glioma", "CNS tumor, pediatric brainstem glioma, recurrent", "childhood CNS tumor, recurrent brain stem glioma", "pediatric CNS tumor, recurrent brain stem glioma", "CNS tumor, recurrent childhood brain stem glioma", "CNS tumor, childhood brainstem glioma, recurrent", "CNS tumor, recurrent brainstem glioma, childhood", "CNS tumor, recurrent brain stem glioma, childhood", "CNS tumor, childhood brain stem glioma, recurrent", "CNS tumor, pediatric brain stem glioma, recurrent", "brain tumor, recurrent brainstem glioma, pediatric", "brain tumor, recurrent brainstem glioma, childhood", "brain tumor, recurrent brain stem glioma, pediatric", "brain tumor, recurrent brain stem glioma, childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Brain Stem Glioma", "shortest_name_length": 27}
{"curie": "MONDO:0012194", "names": ["ANIB3", "intracranial berry aneurysm 3", "aneurysm, intracranial berry, 3", "ANEURYSM, INTRACRANIAL BERRY, 3", "aneurysm, intracranial BERRY, 3", "Aneurysm, Intracranial Berry, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aneurysm, intracranial berry, 3", "shortest_name_length": 5}
{"curie": "UMLS:C1706837", "names": ["Appendix Undifferentiated Carcinoma", "undifferentiated carcinoma of appendix", "undifferentiated carcinoma of appendix (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "undifferentiated carcinoma of appendix", "shortest_name_length": 35}
{"curie": "MONDO:0012667", "names": ["CMD1W", "dilated cardiomyopathy 1W", "Dilated Cardiomyopathy-1W", "Cardiomyopathy, Dilated, 1w", "cardiomyopathy, dilated, 1W", "CARDIOMYOPATHY, DILATED, 1W", "dilated cardiomyopathy type 1W", "cardiomyopathy, dilated, type 1W", "VCL familial isolated dilated cardiomyopathy", "familial isolated dilated cardiomyopathy caused by mutation in VCL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1W", "shortest_name_length": 5}
{"curie": "MONDO:0008418", "names": ["Crest syndrome", "scleroderma, familial progressive", "SCLERODERMA, FAMILIAL PROGRESSIVE", "SYSTEMIC SCLEROSIS, SUSCEPTIBILITY TO", "systemic sclerosis, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scleroderma, familial progressive", "shortest_name_length": 14}
{"curie": "UMLS:C4683547", "names": ["Stage II Adrenal Gland Pheochromocytoma and Sympathetic Paraganglioma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Adrenal Gland Pheochromocytoma and Sympathetic Paraganglioma AJCC v8", "shortest_name_length": 77}
{"curie": "UMLS:C3887521", "names": ["Recurrent Pineoblastoma", "recurrent childhood pineoblastoma", "recurrent pediatric pineoblastoma", "Recurrent Childhood Pineoblastoma", "childhood pineoblastoma, recurrent", "recurrent pineoblastoma, pediatric", "pediatric pineoblastoma, recurrent", "recurrent pineoblastoma, childhood", "pediatric recurrent PNET, pineoblastoma", "childhood recurrent PNET, pineoblastoma", "recurrent pediatric PNET, pineoblastoma", "recurrent childhood PNET, pineoblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Pineoblastoma", "shortest_name_length": 23}
{"curie": "MONDO:0020250", "names": ["OAK", "DOA", "ADOA", "OPA1", "OPTIC ATROPHY 1", "Optic Atrophy 1", "Optic Atrophy 1s", "Kjer Optic Atrophy", "Kjer optic atrophy", "Kjers Optic Atrophy", "Optic atrophy type 1", "Kjer's Optic Atrophy", "Optic Atrophy Type 1", "Atrophy, Kjer's Optic", "Optic Atrophy, Kjer's", "Juvenile Optic Atrophy", "Dominant Optic Atrophy", "dominant optic atrophy", "Atrophy, Juvenile Optic", "KJER-TYPE OPTIC ATROPHY", "Kjer-type Optic Atrophy", "OPTIC ATROPHY, JUVENILE", "Kjer Type Optic Atrophy", "Optic Atrophy, Dominant", "Optic Atrophy, Juvenile", "Kjer-Type Optic Atrophy", "Dominant Optic Atrophies", "OPTIC ATROPHY, KJER TYPE", "Juvenile Optic Atrophies", "Atrophy, Kjer-Type Optic", "Optic Atrophy, Kjer Type", "Optic Atrophy, Kjer-Type", "Optic Atrophies, Dominant", "Optic Atrophies, Juvenile", "Kjer-Type Optic Atrophies", "Atrophies, Juvenile Optic", "Atrophies, Kjer-Type Optic", "Optic Atrophies, Kjer-Type", "Autosomal Dominant Optic Atrophy", "Autosomal dominant optic atrophy", "autosomal dominant optic atrophy", "optic atrophy, autosomal dominant", "Dominant hereditary optic atrophy", "Optic Atrophy, Autosomal Dominant", "optic atrophy hereditary dominant", "Optic atrophy, dominant hereditary", "Autosomal dominant optic atrophy Kjer type", "Autosomal Dominant Optic Atrophy Kjer Type", "Autosomal dominant optic atrophy, Kjer type", "Dominant hereditary optic atrophy (disorder)", "Autosomal dominant optic atrophy classic form", "Dominant hereditary optic atrophy (diagnosis)", "Optic Atrophy, Hereditary, Autosomal Dominant", "optic atrophy hereditary dominant classic form", "Autosomal dominant optic atrophy, classic form", "Autosomal dominant optic atrophy classic form (disorder)", "Autosomal dominant optic atrophy classic form (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant optic atrophy", "shortest_name_length": 3}
{"curie": "UMLS:C4682432", "names": ["Stage IB Vaginal Cancer", "Stage IB Vaginal Cancer AJCC v8", "Stage IB Vaginal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Vaginal Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "UMLS:C3897876", "names": ["Post-Inflammatory Hydrocephalus", "Post Inflammatory Hydrocephalus", "Post inflammatory hydrocephalus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post inflammatory hydrocephalus", "shortest_name_length": 31}
{"curie": "MONDO:0032880", "names": ["DEE82", "EIEE82", "GOT2 DEFICIENCY", "Got2 Deficiency", "early infantile epileptic encephalopathy 82", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 82", "developmental and epileptic encephalopathy 82", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 82", "epileptic encephalopathy, early infantile, 82", "developmental and epileptic encephalopathy, 82", "Glutamate Oxaloacetate Transaminase, Mitochondrial, Deficiency of", "GLUTAMATE OXALOACETATE TRANSAMINASE, MITOCHONDRIAL, DEFICIENCY OF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 82", "shortest_name_length": 5}
{"curie": "MONDO:0032752", "names": ["DEE75", "EIEE75", "early infantile epileptic encephalopathy 75", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 75", "developmental and epileptic encephalopathy 75", "epileptic encephalopathy, early infantile, 75", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 75", "developmental and epileptic encephalopathy, 75"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 75", "shortest_name_length": 5}
{"curie": "UMLS:C1535915", "names": ["Limb crushing injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Limb crushing injury", "shortest_name_length": 20}
{"curie": "MONDO:0010056", "names": ["SMA4", "SMA 4", "SMA-IV", "SMA type 4", "SMA type IV", "spinal muscular atrophy-4", "spinal muscular atrophy 4", "Myelopathic Muscular Atrophy", "Adult spinal muscular atrophy", "Atrophy, Myelopathic Muscular", "adult spinal muscular atrophy", "Muscular Atrophy, Myelopathic", "Adult Spinal Muscular Atrophy", "spinal muscular atrophy type 4", "Muscular Atrophy, Adult Spinal", "spinal muscular atrophy, type 4", "Spinal muscular atrophy type IV", "spinal muscular atrophy, type IV", "Spinal Muscular Atrophy, Type IV", "SPINAL MUSCULAR ATROPHY, TYPE IV", "spinal muscular atrophy of adults", "Adult form spinal muscular atrophy", "SPINAL MUSCULAR ATROPHY, ADULT FORM", "Adult Onset Spinal Muscular Atrophy", "Spinal muscular atrophy adult onset", "spinal muscular atrophy, adult form", "Spinal muscular atrophy, adult form", "Adult-Onset Spinal Muscular Atrophy", "adult-onset spinal muscular atrophy", "atrophy; muscle, spinal, adult form", "muscle; atrophy, spinal, adult form", "Spinal Muscular Atrophy, Adult Form", "Adult onset spinal muscular atrophy", "Proximal spinal muscular atrophy type 4", "proximal spinal muscular atrophy type 4", "Adult spinal muscular atrophy (disorder)", "MUSCULAR ATROPHY, PROXIMAL SPINAL, CHRONIC", "Generalized spinal muscular atrophy of late onset", "Generalised spinal muscular atrophy of late onset", "SPINAL MUSCULAR ATROPHY, PROXIMAL, ADULT, AUTOSOMAL RECESSIVE", "Spinal Muscular Atrophy, Proximal, Adult, Autosomal Recessive", "spinal muscular atrophy, proximal, adult, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal muscular atrophy, type IV", "shortest_name_length": 4}
{"curie": "UMLS:C0280343", "names": ["Stage I Lip and Oral Cavity Squamous Cell Cancer", "Stage I Lip and Oral Cavity Squamous Cell Carcinoma", "oral cavity and lip squamous cell carcinoma, stage I", "lip and oral cavity squamous cell carcinoma, stage I", "epidermoid carcinoma of the lip and oral cavity, stage I", "stage I squamous cell carcinoma of the lip and oral cavity", "Stage I Lip and Oral Cavity Squamous Cell Carcinoma AJCC v7", "squamous cell carcinoma of the lip and oral cavity, stage I", "Stage I Lip and Oral Cavity Squamous Cell Carcinoma AJCC v6", "Stage I Lip and Oral Cavity Squamous Cell Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Lip and Oral Cavity Squamous Cell Carcinoma AJCC v6 and v7", "shortest_name_length": 48}
{"curie": "UMLS:C0242669", "names": ["PLACENTA RETAINED", "Retained placenta", "Retained Placenta", "retained placenta", "placenta retained", "Retained Placentas", "Placenta, Retained", "Placental Retention", "Placentas, Retained", "Retained placenta NOS", "Retained placenta (disorder)", "retained placenta (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Placenta, Retained", "shortest_name_length": 17}
{"curie": "UMLS:C1879279", "names": ["Nasal Type Extranodal NK/T-Cell Lymphoma", "Adult Nasal Type Extranodal NK/T-Cell Lymphoma", "adult nasal type extranodal NK/T-cell lymphoma", "adult nasal type extranodal natural killer/T-cell lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult nasal type extranodal NK/T-cell lymphoma", "shortest_name_length": 40}
{"curie": "UMLS:C5668185", "names": ["Malignant Primary Pelvic Neoplasm", "Primary Malignant Pelvic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Malignant Pelvic Neoplasm", "shortest_name_length": 33}
{"curie": "MONDO:0002801", "names": ["ACPO", "Ogilvie Disease", "OGILVIE SYNDROME", "Ogilvie syndrome", "Ogilvie Syndrome", "ogilvie syndrome", "Syndrome, Ogilvie", "Ogilvie's Syndrome", "ogilvie's syndrome", "Ogilvie's syndrome", "acute colonic ileus", "colon obstruction pseudo", "Colonic Pseudoobstruction", "colonic pseudoobstruction", "False colonic obstruction", "colonic pseudo obstruction", "Pseudoobstruction, Colonic", "Colonic Pseudo-Obstruction", "colonic pseudo-obstruction", "Colonic Pseudo Obstruction", "Colonic pseudo-obstruction", "Pseudo-Obstruction, Colonic", "Pseudo-obstruction of colon", "COLON NOS PSEUDO OBSTRUCTION", "Ogilvie's syndrome (diagnosis)", "acute colonic pseudo-obstruction", "Acute pseudo-obstruction of colon", "Pseudo-obstruction of colon (disorder)", "Acute colonic pseudo-obstruction (ACPO)", "Sympathicotonic colon obstruction syndrome", "primary chronic pseudo-obstruction of colon", "Primary chronic pseudo-obstruction of colon", "Primary chronic pseudo-obstruction of colon (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colonic pseudo-obstruction", "shortest_name_length": 4}
{"curie": "UMLS:C1698398", "names": ["Eosinophilic bronchitis", "Eosinophilic bronchitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eosinophilic bronchitis", "shortest_name_length": 23}
{"curie": "MONDO:0012770", "names": ["HPC15", "Prostate Cancer, Hereditary, 15", "PROSTATE CANCER, HEREDITARY, 15", "prostate cancer, hereditary, 15"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate cancer, hereditary, 15", "shortest_name_length": 5}
{"curie": "UMLS:C0855115", "names": ["Stage III Diffuse Large B-Cell Lymphoma", "Diffuse Large B-Cell Lymphoma Stage III", "Diffuse large B-cell lymphoma stage III", "Ann Arbor Stage III Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Diffuse Large B-Cell Lymphoma", "shortest_name_length": 39}
{"curie": "MONDO:0009857", "names": ["PMDS", "HERNIA UTERI INGUINALE", "Hernia Uteri Inguinale", "hernia uteri inguinale", "Hernia uteri inguinale", "Persistent oviduct syndrome", "PERSISTENT OVIDUCT SYNDROME", "persistent oviduct syndrome", "persistent Müllerian derivatives", "persistent Mullerian derivatives", "Persistent Müllerian derivatives", "Persistent Mullerian Duct Syndrome", "persistent Mullerian duct syndrome", "Persistent Mullerian duct syndrome", "persistent Müllerian duct syndrome", "Persistent Müllerian duct syndrome", "Persistent Müllerian Duct Syndrome", "persistent Muellerian duct syndrome", "Persistent Muellerian duct syndrome", "Pseudohermaphroditism, male internal", "PSEUDOHERMAPHRODITISM, MALE INTERNAL", "pseudohermaphroditism, Male internal", "persistent mullerian duct syndrome, type I", "persistent mullerian duct syndrome, type II", "female genital ducts in otherwise normal male", "FEMALE GENITAL DUCTS IN OTHERWISE NORMAL MALE", "female genital ducts in otherwise normal Male", "Persistent Müllerian duct syndrome (disorder)", "Persistent mullerian duct syndrome, types 1 and 2", "persistent mullerian duct syndrome, types 1 and 2", "PERSISTENT MULLERIAN DUCT SYNDROME, TYPES I AND II", "persistent MULLERIAN duct syndrome, types I and II", "Persistent Mullerian Duct Syndrome, Types I And II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "persistent Mullerian duct syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C5556457", "names": ["Uterine Corpus Inflammatory Myofibroblastic Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Corpus Inflammatory Myofibroblastic Tumor", "shortest_name_length": 49}
{"curie": "MONDO:0002450", "names": ["Prostate adenoma", "Prostate Adenoma", "Prostate.adenoma", "PROSTATE ADENOMA", "prostate adenoma", "Adenoma;prostate", "prostatic adenoma", "adenoma; prostate", "Prostatic adenoma", "Prostatic Adenoma", "adenoma prostatic", "prostate; adenoma", "adenoma - prostate", "Adenoma, Prostatic", "Adenoma - prostate", "Prostatic Adenomas", "adenoma of prostate", "Adenomas, Prostatic", "Adenoma of Prostate", "Adenoma of prostate", "prostate gland adenoma", "adenoma of the prostate", "Adenoma of the Prostate", "Benign adenoma of prostate", "benign adenoma of prostate", "prostatic adenoma (diagnosis)", "Benign adenoma of prostate (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostatic adenoma", "shortest_name_length": 16}
{"curie": "MONDO:0010778", "names": ["CVS", "Cvs-plus", "CVS-Plus", "CVS-PLUS", "periodic vomiting", "cyclical vomiting", "Periodic vomiting", "Cyclical vomiting", "Periodic Vomiting", "Cyclical Vomiting", "Vomiting, periodic", "periodic; vomiting", "vomiting; cyclical", "Vomiting, cyclical", "cyclical; vomiting", "vomiting; periodic", "CYCLIC VOMITING SYNDROME", "cyclic vomiting syndrome", "Cyclic vomiting syndrome", "cyclical vomiting syndrome", "Cyclical Vomiting Syndrome", "cyclical vomiting disorder", "Cyclical vomiting syndrome", "Periodic vomiting syndrome", "vomiting syndrome cyclical", "Cyclic vomiting syndrome NOS", "cyclic vomiting syndrome-plus", "Cyclic Vomiting Syndrome-Plus", "CYCLIC VOMITING SYNDROME-PLUS", "Familial cyclic vomiting syndrome", "cyclic vomiting syndrome (diagnosis)", "Cyclical vomiting syndrome (disorder)", "CYCLIC VOMITING SYNDROME WITH NEUROMUSCULAR DISEASE", "Cyclic Vomiting Syndrome with Neuromuscular Disease", "cyclic vomiting syndrome with neuromuscular disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cyclic vomiting syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C4744850", "names": ["Advanced Kaposi Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Kaposi Sarcoma", "shortest_name_length": 23}
{"curie": "MONDO:0013684", "names": ["VUR6", "VESICOURETERAL REFLUX 6", "vesicoureteral reflux 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vesicoureteral reflux 6", "shortest_name_length": 4}
{"curie": "UMLS:C3146265", "names": ["Prostate cancer stage D", "Stage D Prostate Cancer", "Prostate Cancer Stage D", "stage d prostate cancer", "stage D prostate cancer", "prostate cancer, stage D", "Cancer of Prostate Stage D", "stage D cancer of the prostate", "Cancer of the Prostate Stage D", "cancer of the prostate, stage D", "stage D carcinoma of the prostate", "carcinoma of the prostate, stage D"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate cancer stage D", "shortest_name_length": 23}
{"curie": "MONDO:0027666", "names": ["codeine toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "codeine toxicity", "shortest_name_length": 16}
{"curie": "UMLS:C4528572", "names": ["Stage IA Breast Cancer", "Prognostic Stage IA Breast Cancer AJCC v8", "Prognostic Stage IA Breast Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prognostic Stage IA Breast Cancer AJCC v8", "shortest_name_length": 22}
{"curie": "MONDO:0024623", "names": ["ENT Disease", "ENT disease", "disease, ENT", "ENT disorder", "Disease, ENT", "ENT diseases", "ENT Diseases", "diseases, ENT", "Diseases, ENT", "ear/nose/throat disease", "Otolaryngologic Disease", "otolaryngologic disease", "ENT disorder (diagnosis)", "otolaryngologic diseases", "Otolaryngologic Diseases", "Disease, Otolaryngologic", "disease, otolaryngologic", "Otolaryngologic Disorder", "otolaryngologic disorder", "diseases, otolaryngologic", "otolaryngological disease", "Otolaryngological Disease", "disorders ear nose throat", "Diseases, Otolaryngologic", "otolaryngological diseases", "disorders ears nose throat", "Disease, Otolaryngological", "disease, otolaryngological", "Otolaryngological Diseases", "diseases, otolaryngological", "Diseases, Otolaryngological", "ear, nose or throat disorder", "otorhinolaryngologic disease", "Otorhinolaryngologic Disease", "disease, otorhinolaryngologic", "Ear, nose and throat disorder", "Disease, Otorhinolaryngologic", "Otorhinolaryngologic Diseases", "ear, nose and throat disorder", "otorhinolaryngological disease", "diseases, otorhinolaryngologic", "Otorhinolaryngological Disease", "Diseases, Otorhinolaryngologic", "Otorhinolaryngological Diseases", "otorhinolaryngological diseases", "disease, otorhinolaryngological", "Disease, Otorhinolaryngological", "Diseases, Otorhinolaryngological", "diseases, otorhinolaryngological", "Ear, nose and throat disorder (disorder)", "Disease or syndrome of ear, nose or throat", "Diseases and Syndromes of Ear, Nose and Throat"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "otorhinolaryngologic disease", "shortest_name_length": 11}
{"curie": "UMLS:C5420316", "names": ["Recurrent Hereditary Thyroid Gland Medullary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Hereditary Thyroid Gland Medullary Carcinoma", "shortest_name_length": 54}
{"curie": "UMLS:C0006110", "names": ["Brain Dead", "brain dead", "BRAIN DEATH", "Brain Deads", "Brain death", "death brain", "Brain Death", "brain death", "Death, Brain", "brain deaths", "Coma Depasse", "cerebral death", "brain death (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brain Death", "shortest_name_length": 10}
{"curie": "UMLS:C0543419", "names": ["sequela", "Sequela", "sequelas", "Sequelae", "aftereffect", "late effect", "aftereffects", "late effects", "effects late", "Disease Sequela", "disease sequela", "Pathologic Sequela", "Sequela of disorder", "Sequelae of disorders", "Sequelae of disorders (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sequela of disorder", "shortest_name_length": 7}
{"curie": "MONDO:0019469", "names": ["LGLL", "TLGL", "T-LGL", "LGL Leukemia", "LGL leukemia", "LGL Leukemias", "Leukemia, LGL", "T-LGL Leukemia", "Leukemias, LGL", "T LGL Leukemia", "T-LGL leukemia", "T-LGL Leukemias", "NK LGL Leukemia", "NK-LGL Leukemia", "Leukemia, T-LGL", "Leukemia, T LGL", "NK-LGL Leukemias", "Leukemias, T-LGL", "Leukemia, NK-LGL", "Leukemia, NK LGL", "Leukemias, NK-LGL", "T-cell LGL leukemia", "Aggressive NK Cell Leukemia", "Large granular lymphocytosis", "Large Granular Lymphocytosis", "large granular lymphocytosis", "Large Granular Lymphocytoses", "Granular Lymphocytoses, Large", "Granular Lymphocytosis, Large", "Lymphocytosis, Large Granular", "Lymphocytoses, Large Granular", "T-cell large gran. lymph. leuk.", "Large Granular Lymphocyte Leukemia", "large granular lymphocyte leukemia", "Large granular lymphocyte leukemia", "large granular lymphocytic leukemia", "Large Granular Lymphocytic Leukemia", "T-cell large granular lymphocytosis", "T-gamma lymphoproliferative disease", "Large granular lymphocytic leukemia", "T Gamma Lymphoproliferative Disorder", "Leukemia, Large Granular Lymphocytic", "large granular lymphocytic granuloma", "Large granular lymphocytic leukaemia", "T-gamma lymphoproliferative disorder", "T gamma lymphoproliferative disorder", "T-Gamma Lymphoproliferative Disorder", "large cell granular lymphoid leukemia", "Large Cell Granular Lymphoid Leukemia", "lymphoproliferative; disease, T-gamma", "Leukemia, Lymphocytic, Large Granular", "Aggressive Natural Killer Cell Leukemia", "LGL (large granular lymphocyte) leukemia", "T-cell large granular lymphocyte leukemia", "Large Cell Granular Lymphogenous Leukemia", "Tgamma Large Granular Lymphocyte Leukemia", "T Cell Large Granular Lymphocyte Leukemia", "T-Cell Large Granular Lymphocyte Leukemia", "Tgamma large granular lymphocyte leukemia", "large cell granular lymphogenous leukemia", "T-Cell Large Granular Lymphocytic Leukemia", "T-cell large granular lymphocyte leukaemia", "T Cell Large Granular Lymphocytic Leukemia", "T-cell large granular lymphocytic leukemia", "LGLL - Large granular lymphocytic leukemia", "Large granular T-cell lymphocytic leukemia", "proliferation of large granular lymphocytes", "NK Cell Large Granular Lymphocytic Leukemia", "NK-cell large granular lymphocytic leukemia", "Leukemia, T Cell Large Granular Lymphocytic", "T-cell large granular lymphocytic leukaemia", "Leukemia, T-Cell Large Granular Lymphocytic", "Proliferation of large granular lymphocytes", "NK-Cell Large Granular Lymphocytic Leukemia", "LGLL - Large granular lymphocytic leukaemia", "NK-cell large granular lymphocytic leukaemia", "Large granular lymphocytic leukemia (disorder)", "LEUKEMIA, LARGE GRANULAR LYMPHOCYTIC, MALIGNANT", "leukemia, large granular LYMPHOCYTIC, malignant", "large granular lymphocytic granuloma (diagnosis)", "leukemia lymphocytic chronic T-cell large granular", "Lymphoproliferative Disease of Granular Lymphocytes", "disease (or disorder); lymphoproliferative, T-gamma", "T-cell large granular lymphocytic leukemia (disorder)", "T-cell large granular lymphocytic leukemia (diagnosis)", "leukemia lymphocytic chronic large granular lymphocytic", "Natural Killer Cell Large Granular Lymphocytic Leukemia", "Leukemia, Natural Killer Cell Large Granular Lymphocytic", "Lymphoproliferative Disease of Large Granular Lymphocytes", "T-gamma lymphoproliferative disease (morphologic abnormality)", "T-cell large granular lymphocytic leukemia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-cell large granular lymphocyte leukemia", "shortest_name_length": 4}
{"curie": "UMLS:C1335793", "names": ["Round Cell Liposarcoma NCI Grade 2", "Round Cell Liposarcoma NCI Grade II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Round Cell Liposarcoma NCI Grade 2", "shortest_name_length": 34}
{"curie": "MONDO:0008980", "names": ["BNHS", "Boucher-Neuhäuser syndrome", "Boucher Neuhäuser syndrome", "Boucher-Neuhauser syndrome", "BOUCHER-NEUHAUSER SYNDROME", "Boucher-Neuhauser Syndrome", "Boucher-Neuhchäuser syndrome", "ataxia - hypogonadism - choroidal dystrophy", "Ataxia-hypogonadism-choroidal dystrophy syndrome", "ataxia-hypogonadism-choroidal dystrophy syndrome", "Cerebellar ataxia with hypogonadism and choroidal dystrophy syndrome", "cerebellar ataxia with hypogonadism and choroidal dystrophy syndrome", "Cerebellar ataxia with hypogonadism and choroidal dystrophy syndrome (disorder)", "cerebellar ataxia with hypogonadism and choroidal dystrophy syndrome (diagnosis)", "chorioretinal dystrophy, spinocerebellar ataxia and hypogonadotropic hypogonadism", "SPINOCEREBELLAR ATAXIA, HYPOGONADOTROPIC HYPOGONADISM, AND CHORIORETINAL DYSTROPHY", "Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism", "spinocerebellar ataxia, hypogonadotropic hypogonadism, and chorioretinal dystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ataxia-hypogonadism-choroidal dystrophy syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C1334595", "names": ["Malignant Intrathoracic Paravertebral Paraganglioma", "Metastatic Intrathoracic Paravertebral Paraganglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Intrathoracic Paravertebral Paraganglioma", "shortest_name_length": 51}
{"curie": "UMLS:C1336313", "names": ["Stage II Renal Pelvis Cancer", "Stage II Renal Pelvis Carcinoma", "Stage II Carcinoma of Renal Pelvis", "Stage II Renal Pelvis Cancer AJCC v7", "Stage II Carcinoma of the Renal Pelvis", "Stage II Renal Pelvis Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Renal Pelvis Cancer AJCC v7", "shortest_name_length": 28}
{"curie": "MONDO:0019376", "names": ["West-Nile fever", "West Nile encephalitis", "encephalitis nile west", "West-Nile encephalitis", "west nile encephalitis", "encephalitis west nile", "West Nile virus encephalitis", "fever encephalitis west nile", "West Nile Fever Encephalitis", "West Nile fever encephalitis", "Encephalitis, West Nile Fever", "West Nile fever with encephalitis", "West Nile Fever with encephalitis", "West Nile encephalitis (disorder)", "West Nile virus infectious encephalitis", "West Nile virus infection with encephalitis", "West Nile fever with encephalitis (diagnosis)", "West Nile virus caused infectious encephalitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "West-Nile encephalitis", "shortest_name_length": 15}
{"curie": "MONDO:0009258", "names": ["GALT", "GALAC1", "galactosemia", "GALACTOSEMIA I", "GALT deficiency", "GALT DEFICIENCY", "Galt deficiency", "GALT Deficiency", "Deficiency, GALT", "GALT Deficiencies", "Deficiencies, GALT", "galactosemia type 1", "Galactosemia type 1", "Galactosemia, type I", "Classic galactosemia", "classic galactosemia", "Classic Galactosemia", "Galactosemia, Classic", "GALACTOSEMIA, CLASSIC", "Classic Galactosemias", "galactosemia, classic", "transferase deficiency", "Classical galactosemia", "classical galactosemia", "Galactosemias, Classic", "Classical galactosaemia", "galactosemia, Duarte variant", "GALACTOSEMIA, DUARTE VARIANT", "uridyl transferase deficiency", "Deficiency of uridyl transferase", "Epimerase Deficiency Galactosemia", "Galactosemia, Epimerase Deficiency", "Epimerase Deficiency Galactosemias", "Deficiency Galactosemia, Epimerase", "classical galactosemia (diagnosis)", "Galactosemias, Epimerase Deficiency", "Deficiency Galactosemias, Epimerase", "Transferase deficiency galactosemia", "Transferase deficiency galactosaemia", "classical galactosemia, homozygous Duarte-type", "Classical galactosemia, homozygous Duarte-type", "classical galactosemia, homozygous duarte-type", "Classical galactosaemia, homozygous Duarte-type", "Galactose-1-phosphate uridyltransferase deficiency", "galactose-1-phosphate uridyltransferase deficiency", "Galactose-1-Phosphate Uridyltransferase Deficiency", "Galactose 1 Phosphate Uridyltransferase Deficiency", "Deficiency, Galactose-1-Phosphate Uridyltransferase", "Galactose-1-phosphate uridyl transferase deficiency", "UTP-hexose-1-phosphate uridyltransferase deficiency", "Uridyltransferase Deficiency, Galactose-1-Phosphate", "Galactose-1-Phosphate Uridylyltransferase Deficiency", "Galactose-1-Phosphate Uridyltransferase Deficiencies", "GALACTOSE-1-PHOSPHATE URIDYLYLTRANSFERASE DEFICIENCY", "deficiency; galactose-1-phosphate uridyl transferase", "Galactose 1 Phosphate Uridylyltransferase Deficiency", "Deficiency of hexose-1-phosphate uridylyltransferase", "galactose-1-phosphate uridyl transferase; deficiency", "galactose-1-phosphate uridylyltransferase deficiency", "UTP-Hexose-1-Phosphate Uridylyltransferase Deficiency", "galactose 1 phosphate uridylyl transferase deficiency", "Uridyltransferase Deficiencies, Galactose-1-Phosphate", "Uridylyltransferase Deficiency, Galactose-1-Phosphate", "UTP Hexose 1 Phosphate Uridylyltransferase Deficiency", "UTP Hexose-1-Phosphate Uridylyltransferase Deficiency", "Deficiencies, Galactose-1-Phosphate Uridyltransferase", "Deficiency, Galactose-1-Phosphate Uridylyltransferase", "Deficiency of galactose-1-phosphate uridyl transferase", "Galactose-1-Phosphate Uridylyltransferase Deficiencies", "Uridylyltransferase Deficiencies, Galactose-1-Phosphate", "Deficiencies, Galactose-1-Phosphate Uridylyltransferase", "Deficiency of UTP-hexose-1-phosphate uridylyltransferase", "Classical galactosemia, homozygous Duarte-type (disorder)", "classical galactosemia, homozygous Duarte-type (diagnosis)", "Galactose 1 Phosphate Uridyl Transferase Deficiency Disease", "Galactose-1-Phosphate Uridyl-Transferase Deficiency Disease", "UDPGlucose Hexose-1-Phosphate Uridylyltransferase Deficiency", "UDPGlucose Hexose 1 Phosphate Uridylyltransferase Deficiency", "Deficiency Disease, Galactose 1 Phosphate Uridyl Transferase", "Deficiency Disease, Galactose-1-Phosphate Uridyl-Transferase", "UTP-Hexose-1-Phosphate Uridylyltransferase Deficiency Disease", "UTP Hexose 1 Phosphate Uridylyltransferase Deficiency Disease", "Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase", "Deficiency of uridine triphosphate-hexose-1-phosphate uridylyltransferase", "Deficiency of uridine diphosphate-glucose-hexose-1-phosphate uridylyltransferase", "Deficiency of uridine triphosphate-hexose-1-phosphate uridylyltransferase (disorder)", "Deficiency of uridine diphosphate-glucose-hexose-1-phosphate uridylyltransferase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "classic galactosemia", "shortest_name_length": 4}
{"curie": "MONDO:0006451", "names": ["THYC", "thymoma type C", "Type C thymoma", "Thymoma Type C", "type C thymoma", "thymoma, type C", "Thymoma, type C", "thymus carcinoma", "Thymic Carcinoma", "Thymic carcinoma", "thymic carcinoma", "malignant Thymoma", "Thymic Carcinomas", "Malignant thymoma", "thymic carcinomas", "Carcinoma, Thymic", "Thymoma malignant", "carcinoma; thymic", "thymic; carcinoma", "THYMOMA MALIGNANT", "malignant thymoma", "Malignant Thymoma", "Thymoma, malignant", "thymoma; malignant", "malignant; thymoma", "THYMOMA, MALIGNANT", "Carcinomas, Thymic", "thymoma, malignant", "carcinoma of thymus", "Thymoma malignant NOS", "Type C thymoma (disorder)", "Type C thymoma (diagnosis)", "thymoma and thymic carcinoma", "Thymoma and thymic carcinoma", "Malignant thymoma (disorder)", "thymoma, type C (morphologic abnormality)", "Thymic carcinoma (morphologic abnormality)", "thymoma, malignant (morphologic abnormality)", "Thymoma, malignant (morphologic abnormality)", "thymic carcinoma excluding well differentiated thymic carcinoma", "Thymic Carcinoma Excluding Well Differentiated Thymic Carcinoma", "thymic carcinoma (excluding well differentiated thymic carcinoma)", "Thymic Carcinoma (Excluding Well Differentiated Thymic Carcinoma)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thymic carcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0011793", "names": ["GSES", "CELIAC5", "celiac disease, susceptibility to, 5", "CELIAC DISEASE, SUSCEPTIBILITY TO, 5", "GLUTEN-SENSITIVE ENTEROPATHY, SUSCEPTIBILITY TO, 5", "gluten-sensitive enteropathy, susceptibility to, 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "celiac disease, susceptibility to, 5", "shortest_name_length": 4}
{"curie": "MONDO:0012119", "names": ["ASPG3", "Asperger syndrome susceptibility 3", "ASPERGER syndrome, susceptibility to, 3", "ASPERGER SYNDROME, SUSCEPTIBILITY TO, 3", "asperger syndrome, susceptibility to, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "asperger syndrome, susceptibility to, 3", "shortest_name_length": 5}
{"curie": "MONDO:0009738", "names": ["ML1", "ML 1", "sialidosis", "Neu deficiency", "NEU1 DEFICIENCY", "Neu1 Deficiency", "Neug deficiency", "mucolipidosis 1", "Mucolipidosis I", "Neu1 deficiency", "NEU1 sialidosis", "mucolipidosis I", "nephrosialidosis", "glycoproteinosis", "Nephrosialidosis", "NEU 1 deficiency", "NEPHROSIALIDOSIS", "Sialidosis type 2", "sialidosis type 2", "Sialidosis Type II", "Sialidoses, type 2", "Sialidosis, Type I", "sialidosis, type 1", "Sialidosis, type 2", "sialidosis type II", "SIALIDOSIS, TYPE I", "sialidosis, type I", "sialidosis, type 2", "SIALIDOSIS, TYPE II", "sialidosis, type II", "Sialidosis, Type II", "Mucolipidosis type I", "sialidase deficiency", "mucolipidosis type 1", "mucolipidosis type I", "dysmorphic sialidosis", "Dysmorphic sialidosis", "Neuraminidase Deficiency", "neuraminidase deficiency", "lipomucopolysaccharidosis", "NEURAMINIDASE 1 DEFICIENCY", "neuraminidase 1 deficiency", "Neuraminidase 1 deficiency", "infantile dysmorphic sialidosis", "Infantile dysmorphic sialidosis", "Dysmorphic sialidosis (disorder)", "myoclonus--cherry Red spot syndrome", "cherry Red spot--myoclonus syndrome", "sialidosis caused by mutation in NEU1", "glycoprotein neuraminidase deficiency", "Dysmorphic sialidosis with renal involvement", "dysmorphic sialidosis with renal involvement", "Dysmorphic sialidosis with renal involvement (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sialidosis type 2", "shortest_name_length": 3}
{"curie": "MONDO:0021459", "names": ["benign esophagus tumor", "Benign Esophagus Tumor", "benign esophagus tumors", "Benign Esophageal Tumor", "benign esophageal tumor", "Esophageal benign tumor", "Esophageal tumor benign", "benign esophageal tumors", "Benign tumor of esophagus", "Oesophageal tumour benign", "esophagus benign neoplasm", "Benign Esophagus Neoplasm", "Benign Tumor of Esophagus", "benign esophagus neoplasm", "benign tumor of esophagus", "Benign esophageal neoplasm", "Benign Esophageal Neoplasm", "benign esophageal neoplasm", "Benign oesophageal neoplasm", "Benign tumour of oesophagus", "Benign Neoplasm of Esophagus", "benign neoplasm of esophagus", "Benign neoplasm of esophagus", "Benign neoplasm of oesophagus", "benign tumor of the esophagus", "Benign Tumor of the Esophagus", "Benign Neoplasm of the Esophagus", "benign neoplasm of the esophagus", "Benign neoplasm of esophagus, NOS", "Benign neoplasm of oesophagus, NOS", "Benign neoplasm of esophagus (disorder)", "benign neoplasm of esophagus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of esophagus", "shortest_name_length": 22}
{"curie": "UMLS:C0855058", "names": ["Relapsed Leiomyosarcoma", "Leiomyosarcoma Recurrent", "Recurrent Leiomyosarcoma", "Leiomyosarcoma recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leiomyosarcoma recurrent", "shortest_name_length": 23}
{"curie": "MONDO:0003139", "names": ["mesangial proliferative GN", "Mesangioproliferative glomerulonephritis", "Mesangial Proliferative Glomerulonephritis", "mesangial proliferative glomerulonephritis", "Mesangial proliferative glomerulonephritis", "glomerulonephritis mesangial proliferative", "GLOMERULONEPHRITIS, MESANGIAL PROLIFERATIVE", "Glomerulonephritis, mesangial proliferative", "glomerulonephritis - mesangial proliferative", "Mesangial proliferative glomerulonephritis (disorder)", "Mesangial proliferative glomerulonephritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mesangial proliferative glomerulonephritis", "shortest_name_length": 26}
{"curie": "MONDO:0020977", "names": ["granulomatous prostatitis", "prostatitis granulomatous", "Granulomatous Prostatitis", "Granulomatous prostatitis", "prostatitis; granulomatous", "granulomatous; prostatitis", "Prostatitis, granulomatous", "Granulomatous prostatitis (disorder)", "granulomatous prostatitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "granulomatous prostatitis", "shortest_name_length": 25}
{"curie": "UMLS:C1708956", "names": ["Mediastinal Myeloid Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mediastinal Myeloid Sarcoma", "shortest_name_length": 27}
{"curie": "UMLS:C3898652", "names": ["Myocardial infarction type 5", "TYPE 5 MYOCARDIAL INFARCTION", "Joint Task Force Type 5 Myocardial Infarction", "Joint ESC/ACCF/AHA/WHF Task Force Type 5 Myocardial Infarction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joint Task Force Type 5 Myocardial Infarction", "shortest_name_length": 28}
{"curie": "MONDO:0013711", "names": ["PNMHH", "peripheral neuropathy-myopathy-hoarseness-deafness syndrome", "peripheral neuropathy, myopathy, hoarseness, and hearing loss", "PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS", "peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C1333465", "names": ["Esophageal Precancerous Condition", "Esophageal Premalignant Condition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Precancerous Condition", "shortest_name_length": 33}
{"curie": "MONDO:0019801", "names": ["adrenal storm", "ADRENAL STORM", "adrenal crisis", "Adrenal Crisis", "Crisis adrenal", "Adrenal crisis", "ADRENAL CRISIS", "CRISIS ADRENAL", "shock; adrenal", "adrenal; shock", "crisis; adrenal", "Addison; crisis", "adrenal; crisis", "crisis; Addison", "ADRENAL APOPLEXY", "Adrenal Apoplexy", "collapse; adrenal", "ADDISONIAN CRISIS", "addisonian crisis", "Addisonian Crisis", "adrenal; collapse", "CRISIS ADDISONIAN", "Addisonian crisis", "adrenocortical crisis", "acute adrenal failure", "Acute adrenal failure", "Adrenocortical crisis", "Adrenal crisis syndrome", "adrenal crisis (diagnosis)", "acute adrenal insufficiency", "Acute adrenal insufficiency", "Acute Adrenal Insufficiency", "severe adrenal insufficiency", "Severe adrenal insufficiency", "Addisonian crisis (diagnosis)", "acute adrenocortical insufficiency", "Adrenocortical insufficiency acute", "Acute adrenocortical insufficiency", "ADRENOCORTICAL INSUFFICIENCY, ACUTE", "Acute adrenal insufficiency (disorder)", "Severe adrenal insufficiency (disorder)", "Adrenocortical insufficiency syndrome, acute"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute adrenal insufficiency", "shortest_name_length": 13}
{"curie": "UMLS:C1337019", "names": ["Well Differentiated Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Well Differentiated Malignant Neoplasm", "shortest_name_length": 38}
{"curie": "MONDO:0015772", "names": ["trisomy 8q", "Trisomy 8q", "8q trisomy", "8q+ syndrome", "8q duplication", "Duplication 8q", "trisomy type 8q", "dup(8q) syndrome", "partial trisomy 8q", "chromosome 8q trisomy", "8q duplication syndrome", "duplication 8q syndrome", "Chromosome 8, trisomy 8q", "chromosome 8q duplication", "chromosome 8q duplication syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trisomy 8q", "shortest_name_length": 10}
{"curie": "MONDO:0010248", "names": ["SEMDX", "SEMD X-linked", "SEMD, X-LINKED", "SEMD, X-Linked", "SEMD, X-linked", "spondylo-epimetaphyseal dysplasia", "spondyloepimetaphyseal dysplasia X-linked", "X-linked spondyloepimetaphyseal dysplasia", "X-Linked Spondyloepimetaphyseal Dysplasia", "SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED", "Spondyloepimetaphyseal Dysplasia, X-Linked", "spondyloepimetaphyseal dysplasia, X-linked", "X-linked spondyloepimetaphyseal dysplasia (disorder)", "spondyloepimetaphyseal dysplasia, X-linked, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked spondyloepimetaphyseal dysplasia", "shortest_name_length": 5}
{"curie": "UMLS:C0347391", "names": ["Skin appendage tumor, benign", "Benign Skin Appendage Neoplasm", "Benign Epidermal Appendage Tumor", "Benign neoplasm of adnexa of skin", "Benign Cutaneous Adnexal Neoplasm", "Benign Tumor of Epidermal Appendage", "Benign Epidermal Appendage Neoplasm", "Benign tumor of epidermal appendage", "Benign tumour of epidermal appendage", "Benign Neoplasm of Epidermal Appendage", "Benign Tumor of the Epidermal Appendage", "Benign Neoplasm of the Epidermal Appendage", "Benign neoplasm of adnexa of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign neoplasm of adnexa of skin", "shortest_name_length": 28}
{"curie": "MONDO:0016370", "names": ["MBD", "bone loss", "Bone Loss", "Bone loss", "Osteopenia", "bone; loss", "loss; bone", "osteopenia", "OSTEOPENIA", "Osteopenias", "Marchiafava", "Osteopaenia", "Low Bone Density", "Bone Density, Low", "Bone demineralized", "Low Bone Densities", "Marchiafava disease", "MARCHIAFAVA DISEASE", "marchiafava disease", "Osteopenia (disorder)", "generalize osteopenia", "Generalised osteopenia", "METABOLIC BONE DISEASE", "Metabolic bone disease", "Generalized osteopenia", "OSTEOPENIA GENERALIZED", "osteopenia (diagnosis)", "Metabolic Bone Disease", "generalized osteopenia", "metabolic bone disease", "Metabolic Bone Diseases", "Bone Disease, Metabolic", "Metabolic Bone Disorder", "metabolic bone diseases", "Osteopenia, generalized", "metabolic bone disorder", "Low Bone Mineral Density", "Bone metabolism disorder", "bone disorders metabolic", "Bone Diseases, Metabolic", "metabolic bone disorders", "bone metabolism disorder", "Low bone mineral density", "Metabolic bone disorders", "Osteopenia/ Osteoporosis", "Bone metabolism disorders", "Metabolic disorder of bone", "Marchiafava Bignami disease", "Metabolic bone disease, NOS", "Marchiafava Bignami Disease", "Marchiafava-Bignami Disease", "Marchiafava-Bignami disease", "marchiafava-bignami disease", "marchiafava-bignami syndrome", "Marchiafava-Bignami Syndrome", "MARCHIAFAVA-BIGNAMI SYNDROME", "Marchiafava Bignami Syndrome", "Bones--Metabolism--Disorders", "corpus callosum; demyelination", "Decreased bone mineral density", "demyelination; corpus callosum", "Callosum degeneration syndrome", "acute Marchiafava-Bignami disease", "Metabolic bone disease (disorder)", "metabolic bone disease (diagnosis)", "Osteopenia (morphologic abnormality)", "chronic Marchiafava-Bignami syndrome", "Marchiafava-Bignami disease (disorder)", "ENCEPHALOPATHY, CALLOSAL DEMYELINATING", "encephalopathy; demyelinating callosal", "Marchiafava-Bignami disease (diagnosis)", "Central demyelination of corpus callosum", "central demyelination of corpus callosum", "central demyelination of corpus callosum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Marchiafava-Bignami disease", "shortest_name_length": 3}
{"curie": "MONDO:0007685", "names": ["GRANULOSIS RUBRA NASI", "Granulosis Rubra Nasi", "granulosis rubra nasi", "Granulosis rubra nasi", "Granulosis rubra nasi (disorder)", "granulosis rubra nasi (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "granulosis rubra nasi", "shortest_name_length": 21}
{"curie": "UMLS:C4521905", "names": ["Stage IV Hepatocellular Cancer", "Stage IV Hepatocellular Carcinoma", "Stage IV Hepatocellular Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Hepatocellular Carcinoma AJCC v7", "shortest_name_length": 30}
{"curie": "UMLS:C4683419", "names": ["Stage II Differentiated Thyroid Gland Cancer Under 55 Years", "Stage II Differentiated Thyroid Gland Carcinoma Under 55 Years AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Differentiated Thyroid Gland Carcinoma Under 55 Years AJCC v8", "shortest_name_length": 59}
{"curie": "UMLS:C1266102", "names": ["Unclassified Testicular Sex Cord-Stromal Tumor", "Unclassified Testicular Sex Cord-Gonadal Stromal Tumor", "Sex cord-gonadal stromal tumor, incompletely differentiated", "Sex Cord-Gonadal Stromal Tumor, Incompletely Differentiated", "Sex cord-gonadal stromal tumour, incompletely differentiated", "Testicular Sex Cord-Gonadal Stromal Tumor, Incompletely Differentiated", "Testicular Sex Cord-Gonadal Stromal Tumor with Indeterminate Differentiation", "Sex cord-gonadal stromal tumor, incompletely differentiated (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular Sex Cord-Gonadal Stromal Tumor, Incompletely Differentiated", "shortest_name_length": 46}
{"curie": "MONDO:0043112", "names": ["lachiewicz sibley syndrome", "Lachiewicz Sibley syndrome", "Hereditary renal disease and preauricular pits", "hereditary renal disease and preauricular pits"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lachiewicz sibley syndrome", "shortest_name_length": 26}
{"curie": "MONDO:0002684", "names": ["ACPP", "Atypical CPP", "atypical CPP", "Atypical choroid plexus papilloma", "Atypical Choroid Plexus Papilloma", "atypical choroid plexus papilloma", "Atypical papilloma of choroid plexus", "atypical papilloma of choroid plexus", "Atypical papilloma of choroid plexus (disorder)", "atypical choroid plexus papilloma (morphologic abnormality)", "Atypical choroid plexus papilloma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical choroid plexus papilloma", "shortest_name_length": 4}
{"curie": "MONDO:0017170", "names": ["idiopathic recurrent stupor", "Idiopathic recurrent stupor", "Idiopathic recurrent stupor (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic recurrent stupor", "shortest_name_length": 27}
{"curie": "UMLS:C0750936", "names": ["Intracranial Astrocytoma", "Intracranial Astrocytomas", "Astrocytoma, Intracranial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intracranial Astrocytoma", "shortest_name_length": 24}
{"curie": "MONDO:0600019", "names": ["TBX4 acinar dysplasia", "TBX4 related acinar dysplasia", "acinar dysplasia caused by mutation in TBX4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acinar dysplasia caused by mutation in TBX4", "shortest_name_length": 21}
{"curie": "UMLS:C1709844", "names": ["Reactive C-Cell Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reactive C-Cell Hyperplasia", "shortest_name_length": 27}
{"curie": "MONDO:0014654", "names": ["UCMD2", "Ullrich congenital muscular dystrophy 2", "ULLRICH CONGENITAL MUSCULAR DYSTROPHY 2", "Ullrich congenital muscular dystrophy type 2", "COL12A1 Ullrich congenital muscular dystrophy", "Ullrich congenital muscular dystrophy caused by mutation in COL12A1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ullrich congenital muscular dystrophy 2", "shortest_name_length": 5}
{"curie": "MONDO:0001202", "names": ["prostate cyst", "prostatic cyst", "prostate; cyst", "cysts prostate", "Prostatic cyst", "cyst; prostate", "cyst of prostate", "Cyst of prostate", "prostate cyst (diagnosis)", "Cyst of prostate (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostatic cyst", "shortest_name_length": 13}
{"curie": "UMLS:C4721669", "names": ["stage IV laryngeal cancer", "Stage IV Laryngeal Throat Cancer", "Stage IV Laryngeal Cancer AJCC v6", "Stage IV Larynx Carcinoma AJCC v6", "Laryngeal Cancer, Stage IV AJCC v6", "Stage IV Carcinoma of Larynx AJCC v6", "Stage IV Laryngeal Carcinoma AJCC v6", "Stage IV Carcinoma of the Larynx AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Laryngeal Cancer AJCC v6", "shortest_name_length": 25}
{"curie": "MONDO:0011282", "names": ["Tsg11", "TSG11", "nonsmall cell lung cancer", "Nonsmall cell lung cancer suppressor", "NONSMALL CELL LUNG CANCER SUPPRESSOR", "tumor suppressor gene on chromosome 11", "TUMOR SUPPRESSOR GENE ON CHROMOSOME 11", "tumor suppressor Gene on chromosome type 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tumor suppressor gene on chromosome 11", "shortest_name_length": 5}
{"curie": "MONDO:0100367", "names": ["nova syndrome", "port-wine nevi-mega cisterna magna-hydrocephalus syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "port-wine nevi-mega cisterna magna-hydrocephalus syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0004090", "names": ["vulvar basaloid carcinoma", "Vulvar Basaloid Carcinoma", "Vulvar Basaloid Squamous Cell Carcinoma", "vulvar basaloid squamous cell carcinoma", "basaloid squamous cell carcinoma of vulva", "basaloid squamous cell carcinoma of vulva (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar basaloid squamous cell carcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0011556", "names": ["BCC1", "Multiple basal cell carcinoma", "multiple basal cell carcinoma", "basal cell carcinoma, somatic", "basal cell carcinoma, multiple", "Basal cell carcinoma, multiple", "BASAL CELL CARCINOMA, MULTIPLE", "BASAL CELL CARCINOMA, NONSYNDROMIC", "basal cell carcinoma, nonsyndromic", "Basal Cell Carcinoma, Nonsyndromic", "BASAL CELL CARCINOMA, SUSCEPTIBILITY TO, 1", "basal cell carcinoma, susceptibility to, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "basal cell carcinoma, susceptibility to, 1", "shortest_name_length": 4}
{"curie": "UMLS:C4054389", "names": ["Nephrotic Syndrome - DGKE Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - DGKE Associated", "shortest_name_length": 36}
{"curie": "MONDO:0003019", "names": ["HYPOKALEMIA", "hypokalemia", "Hypokalemia", "hypokalaemia", "Hypokalemias", "HYPOKALAEMIA", "Hypokalaemia", "k deficiency", "hypokalemias", "deficiency k", "hypopotassemia", "HYPOPOTASSEMIA", "Hypopotassemia", "HYPOPOTASSAEMIA", "Hypopotassemias", "Hypopotassaemia", "hypopotassaemia", "Potassium depletion", "potassium depletion", "potassium; depletion", "depletion; potassium", "SYNDROME HYPOKALEMIC", "Syndrome hypokalemic", "Hypokalemic syndrome", "Hypokalemic disorder", "potassium deficiency", "HYPOKALEMIC SYNDROME", "deficiency potassium", "syndrome; hypokalemic", "Hypokalaemic syndrome", "Syndrome hypokalaemic", "hypokalemic; syndrome", "LOW POTASSIUM SYNDROME", "Hypokalemia (disorder)", "Low potassium syndrome", "HYPOPOTASSEMIA SYNDROME", "hypokalemia (diagnosis)", "Hypopotassemia syndrome", "Potassium [K] deficiency", "Hypopotassaemia syndrome", "Low serum potassium level", "low blood potassium level", "blood levels low potassium", "Low blood potassium levels", "potassium deficiency disease", "potassium deficiency disorder", "Potassium Deficiency Disorder", "Serum potassium level below reference range", "Serum potassium concentration decreased below normal", "Serum potassium level below reference range (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "potassium deficiency disease", "shortest_name_length": 11}
{"curie": "UMLS:C0000823", "names": ["Veterinary Abortion", "Veterinary Abortions", "Abortion, Veterinary", "Abortions, Veterinary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abortion, Veterinary", "shortest_name_length": 19}
{"curie": "UMLS:C5418596", "names": ["Advanced Anal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Anal Carcinoma", "shortest_name_length": 23}
{"curie": "UMLS:C0345203", "names": ["Large Intestine Atresia", "Atresia of large intestine", "atresia of large intestine", "Atresia of Large Intestine", "Atresia of the Large Intestine", "Congenital Large Intestinal Atresia", "Congenital large intestinal atresia", "Atresia of large intestine (disorder)", "Congenital atresia of large intestine", "atresia of large intestine (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital atresia of large intestine", "shortest_name_length": 23}
{"curie": "UMLS:C0238022", "names": ["bladder foreign body", "BLADDER, FOREIGN BODY", "foreign body; bladder", "Foreign body in bladder", "foreign body of bladder", "Foreign Body in Bladder", "FB - Foreign body of bladder", "Foreign body in bladder (disorder)", "foreign body of bladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Foreign body in bladder", "shortest_name_length": 20}
{"curie": "MONDO:0008967", "names": ["Cbas4", "CBAS4", "BASD4", "AMACR deficiency", "BAS defect type 4", "trihydroxycoprostanic acid in bile", "Trihydroxycoprostanic acid in bile", "TRIHYDROXYCOPROSTANIC ACID IN BILE", "2-methylacyl-CoA racemase deficiency", "congenital bile acid synthesis defect 4", "BILE ACID SYNTHESIS DEFECT, CONGENITAL, 4", "Trihydroxycoprostanic acid to cholic acid", "Alpha-methyl-acyl-CoA racemase deficiency", "bile acid synthesis defect, congenital, 4", "Bile acid synthesis defect, congenital, 4", "congenital bile acid synthesis defect type 4", "bile acid synthesis defect, congenital, type 4", "cholestasis, intrahepatic, with defective conversion of", "liver disease-retinitis pigmentosa-polyneuropathy-epilepsy syndrome", "intrahepatic cholestasis with defective conversion of trihydroxycoprostanic acid to cholic acid", "Cholestasis, intrahepatic, with defective conversion of Trihydroxycoprostanic acid to cholic acid", "CHOLESTASIS, INTRAHEPATIC, WITH DEFECTIVE CONVERSION OF TRIHYDROXYCOPROSTANIC ACID TO CHOLIC ACID", "cholestasis, intrahepatic, with defective conversion of Trihydroxycoprostanic acid to cholic acid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital bile acid synthesis defect 4", "shortest_name_length": 5}
{"curie": "UMLS:C1709580", "names": ["Pleural WDPM", "Pleural WDPMT", "Pleural Well Differentiated Papillary Mesothelioma", "Pleural Well-Differentiated Papillary Mesothelioma", "Pleural Well-Differentiated Papillary Mesothelial Tumor", "Pleural Well Differentiated Papillary Mesothelial Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pleural Well Differentiated Papillary Mesothelial Tumor", "shortest_name_length": 12}
{"curie": "MONDO:0016224", "names": ["autosomal dominant proximal spinal muscular atrophy", "proximal spinal muscular atrophy, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant proximal spinal muscular atrophy", "shortest_name_length": 51}
{"curie": "UMLS:C4683607", "names": ["Lugano Classification Stage I Adult Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage I Adult Hodgkin Lymphoma AJCC v8", "shortest_name_length": 60}
{"curie": "UMLS:C0542241", "names": ["toxemia", "Toxemia", "Bacterial toxemia", "Bacterial Toxemia", "Toxemia bacterial", "TOXEMIA BACTERIAL", "Bacterial toxaemia", "Toxaemia bacterial", "Toxemia bacterial NOS", "Toxaemia bacterial NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bacterial Toxemia", "shortest_name_length": 7}
{"curie": "MONDO:0000824", "names": ["congenital diarrhea", "diarrhea, congenital"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital diarrhea", "shortest_name_length": 19}
{"curie": "MONDO:0054844", "names": ["PCH1D", "pontocerebellar hypoplasia type 1D", "pontocerebellar hypoplasia, type 1D", "PONTOCEREBELLAR HYPOPLASIA, TYPE 1D"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pontocerebellar hypoplasia, type 1D", "shortest_name_length": 5}
{"curie": "MONDO:0008278", "names": ["JPHT", "JPSHHT", "JP-HHT", "jPS/Hht", "JPS/HHT", "JPHHT Syndrome", "JP/Hht syndrome", "JP/HHT SYNDROME", "juvenile polyposis / hemorrhagic telangiectasia syndrome", "Juvenile Polyposis with Hereditary Hemorrhagic Telangiectasia", "JUVENILE POLYPOSIS WITH HEREDITARY HEMORRHAGIC TELANGIECTASIA", "juvenile polyposis with hereditary hemorrhagic telangiectasia", "JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME", "juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome", "juvenile polyposis-hereditary hemorrhagic telangiectasia syndrome", "Juvenile Polyposis Hereditary Hemorrhagic Telangiectasia Syndrome", "juvenile polyposis / hemorrhagic telangiectasia syndrome (diagnosis)", "telangiectasia, hereditary hemorrhagic, with juvenile polyposis coli", "Telangiectasia, Hereditary Hemorrhagic, with Juvenile Polyposis Coli", "TELANGIECTASIA, HEREDITARY HEMORRHAGIC, WITH JUVENILE POLYPOSIS COLI", "Juvenile polyposis syndrome with hereditary hemorrhagic telangiectasia", "Juvenile polyposis syndrome with hereditary haemorrhagic telangiectasia", "polyposis, generalized juvenile, with pulmonary arteriovenous malformation", "POLYPOSIS, GENERALIZED JUVENILE, WITH PULMONARY ARTERIOVENOUS MALFORMATION", "Polyposis, Generalized Juvenile, with Pulmonary Arteriovenous Malformation", "JP-HHT (juvenile polyposis with hereditary hemorrhagic telangiectasia) syndrome", "JP-HHT (juvenile polyposis with hereditary haemorrhagic telangiectasia) syndrome", "Juvenile polyposis syndrome with hereditary hemorrhagic telangiectasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0011084", "names": ["PSORS3", "psoriasis 3", "PSORIASIS SUSCEPTIBILITY 3", "psoriasis susceptibility 3", "PSORIASIS 3, SUSCEPTIBILITY TO", "psoriasis 3, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "psoriasis 3, susceptibility to", "shortest_name_length": 6}
{"curie": "UMLS:C5668165", "names": ["Pleural Mesothelioma In Situ"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pleural Mesothelioma In Situ", "shortest_name_length": 28}
{"curie": "UMLS:C0861218", "names": ["Stage II Centroblastic Lymphoma", "Centroblastic lymphoma stage II", "Ann Arbor Stage II Centroblastic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Centroblastic lymphoma stage II", "shortest_name_length": 31}
{"curie": "EFO:1001494", "names": ["psoriasis vulgaris"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "psoriasis vulgaris", "shortest_name_length": 18}
{"curie": "MONDO:0010516", "names": ["MFHIEN", "midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis", "MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS", "midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis; MFHIEN", "midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis", "shortest_name_length": 6}
{"curie": "MONDO:0007753", "names": ["Frey", "HYPRG", "frey syndrome", "Frey Syndrome", "Frey syndrome", "FREY SYNDROME", "Syndrome, Frey", "DUPUY SYNDROME", "freys syndrome", "Frey's syndrome", "frei's syndrome", "Frey's Syndrome", "frey's syndrome", "Syndrome, Frey's", "von Frey Syndrome", "GUSTATORY SWEATING", "gustatory sweating", "Gustatory Sweating", "Syndrome, von Frey", "Gustatory sweating", "von Freys Syndrome", "von frey's syndrome", "Baillarger syndrome", "Sweating, Gustatory", "Baillarger Syndrome", "von Frey's syndrome", "von Frey's Syndrome", "Syndrome, von Frey's", "Syndrome, Baillarger", "hyperhidrosis gustatory", "Gustatory Hyperhidrosis", "Gustatory Hyperhidroses", "Gustatory hyperhidrosis", "gustatory hyperhidrosis", "hyperhidrosis, gustatory", "FREY-BAILLARGER SYNDROME", "HYPERHIDROSIS, GUSTATORY", "Hyperhidrosis, Gustatory", "Hyperhidroses, Gustatory", "Auriculotemporal Syndrome", "Auriculotemporal syndrome", "AURICULOTEMPORAL SYNDROME", "Syndrome, Auriculotemporal", "Gustatory sweating syndrome", "gustatory sweating syndrome", "Salivosudoriparous Syndrome", "GUSTATORY SWEATING SYNDROME", "Frey's syndrome (diagnosis)", "Syndrome, Salivosudoriparous", "Salivosudoriparous Syndromes", "gustatory sweating; syndrome", "Gustatory sweating (finding)", "syndrome; gustatory sweating", "Syndromes, Salivosudoriparous", "auriculotemporal nerve syndrome", "Auriculotemporal Nerve Syndrome", "AURICULOTEMPORAL NERVE SYNDROME", "Gustatory hyperhidrosis (disorder)", "Auriculotemporal syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Frey syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0008332", "names": ["VWDP", "PT-VWD", "BDPLT3", "Pseudo-von Willebrand Disease", "Pseudo-von Willebrand disease", "Pseudo-Von Willebrand disease", "Pseudo von Willebrand disease", "PSEUDO-VON WILLEBRAND DISEASE", "pseudo-VON WILLEBRAND disease", "pseudo-von Willebrand disease", "platelet-type bleeding disorder 3", "von Willebrand disease, pseudo type", "bleeding disorder, Platelet-type, 3", "BLEEDING DISORDER, PLATELET-TYPE, 3", "platelet-type von Willebrand disease", "Platelet-Type von Willebrand Disease", "Platelet type von Willebrand disease", "Platelet-type von Willebrand disease", "Platelet-type Von Willebrand disease", "von Willebrand disease platelet-type", "Platelet type-von Willebrand disease", "platelet type-von Willebrand disease", "VON WILLEBRAND DISEASE, PLATELET-TYPE", "Von Willebrand disease, Platelet-type", "Pseudo-von Willebrand disease type 2B", "Von Willebrand disease, platelet type", "Von Willebrand Disease, Platelet-Type", "pseudo-von Willebrand disease type 2B", "von Willebrand disease, platelet type", "Platelet type von Willebrand's disease", "Pseudo von Willebrand disease (disorder)", "Platelet type pseudo-von Willebrand disease", "PT-VWD - platelet type-von Willebrand disease", "Platelet type von Willebrand's disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "platelet-type von Willebrand disease", "shortest_name_length": 4}
{"curie": "MONDO:0022639", "names": ["Cantu sanchez-corona Garcia-Cruz syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cantu sanchez-corona Garcia-Cruz syndrome", "shortest_name_length": 41}
{"curie": "MONDO:0700025", "names": ["chromosome 20 disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 20 disorder", "shortest_name_length": 22}
{"curie": "UMLS:C1711320", "names": ["Appendix Signet Ring Cell Carcinoma", "Appendix Signet-Ring Cell Carcinoma", "signet ring cell carcinoma of appendix", "signet ring cell carcinoma of appendix (diagnosis)", "appendiceal neoplasm malignant carcinoma signet ring cell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "signet ring cell carcinoma of appendix", "shortest_name_length": 35}
{"curie": "MONDO:0021483", "names": ["benign frontal sinus tumor", "Benign Frontal Sinus Tumor", "frontal sinus benign neoplasm", "Benign Frontal Sinus Neoplasm", "benign frontal sinus neoplasm", "Benign Tumor of Frontal Sinus", "Benign tumor of frontal sinus", "benign tumor of frontal sinus", "Benign tumour of frontal sinus", "benign neoplasm of frontal sinus", "Benign Neoplasm of Frontal Sinus", "Benign neoplasm of frontal sinus", "Benign Tumor of the Frontal Sinus", "benign tumor of the frontal sinus", "benign neoplasm of the frontal sinus", "Benign Neoplasm of the Frontal Sinus", "Benign neoplasm of frontal sinus (disorder)", "benign neoplasm of frontal sinus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of frontal sinus", "shortest_name_length": 26}
{"curie": "MONDO:0015135", "names": ["primary immunodeficiency due to a defect in innate immunity", "primary immunodeficiency due to a genetic defect in innate immunity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary immunodeficiency due to a genetic defect in innate immunity", "shortest_name_length": 59}
{"curie": "MONDO:0022759", "names": ["22 trisomy", "TRISOMY 22", "Trisomy 22", "trisomy 22", "trisomy; 22", "Duplication 22", "Trisomy 22 syndrome", "chromosome 22 trisomy", "trisomy; syndrome, 22", "syndrome; trisomy, 22", "Trisomy 22 (disorder)", "trisomy 22 (diagnosis)", "Chromosome 22, trisomy", "chromosome; 22, trisomy", "Complete trisomy 22 syndrome", "chromosome 22 trisomy syndrome", "Complete trisomy 22 syndrome (disorder)", "Chromosomal imbalance syndrome, pair 22, trisomy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trisomy 22", "shortest_name_length": 10}
{"curie": "MONDO:0019885", "names": ["Trisomy 11qter", "trisomy 11qter", "distal trisomy 11q", "Distal Trisomy 11q", "Distal trisomy 11q", "11q Partial Trisomy", "Distal duplication 11q", "distal duplication 11q", "distal trisomy type 11q", "Telomeric duplication 11q", "telomeric duplication 11q", "Distal trisomy 11q (disorder)", "Distal trisomy 11q (diagnosis)", "Chromosome 11, partial trisomy 11q", "anomaly of chromosome pair 11q partial trisomy syndrome distal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal trisomy 11q", "shortest_name_length": 14}
{"curie": "UMLS:C0265911", "names": ["Pulmonary artery stenosis", "Stenosis of pulmonary artery", "congenital pulmonary stenosis", "Congenital pulmonary stenosis", "Stenosis;pulmonary;congenital", "a.pulmonalis; stricture, congenital", "Pulmonary artery stenosis congenital", "Congenital Pulmonary Artery Stenosis", "Congenital pulmonary artery stenosis", "Congenital narrowed pulmonary artery", "congenital; stricture, pulmonary artery", "Congenital stenosis of pulmonary artery", "stricture; artery, congenital, pulmonary", "stricture; pulmonary artery (congenital)", "Congenital stricture of pulmonary artery", "stricture; pulmonary, artery (congenital)", "Congenital stenosis of pulmonary artery (disorder)", "pulmonary; stricture pulmonary artery (congenital)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital stenosis of pulmonary artery", "shortest_name_length": 25}
{"curie": "MONDO:0005142", "names": ["Pseudomonas aeruginosa CF5 infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pseudomonas aeruginosa CF5 infection", "shortest_name_length": 36}
{"curie": "MONDO:0033564", "names": ["OOMD8", "oocyte maturation defect 8", "OOCYTE MATURATION DEFECT 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oocyte maturation defect 8", "shortest_name_length": 5}
{"curie": "UMLS:C5667188", "names": ["Recurrent Epstein-Barr Virus-Related Lymphoproliferative Disease with Primary Immunodeficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Epstein-Barr Virus-Related Lymphoproliferative Disease with Primary Immunodeficiency", "shortest_name_length": 94}
{"curie": "MONDO:0013732", "names": ["GCTR", "GLUCOCORTICOID THERAPY, RESPONSE TO", "glucocorticoid therapy, response to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glucocorticoid therapy, response to", "shortest_name_length": 4}
{"curie": "MONDO:0010467", "names": ["dup(X)(q27.3q28)", "trisomy Xq27.3q28", "trisomy Xq27.3-q28", "Xq27.3q28 duplication syndrome", "Xq27.3-q28 microduplication syndrome", "CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME", "chromosome Xq27.3-q28 DUPLICATION syndrome", "chromosome xq27.3-q28 duplication syndrome, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Xq27.3q28 duplication syndrome", "shortest_name_length": 16}
{"curie": "UMLS:C5239288", "names": ["Cutaneous Indeterminate Cell Histiocytosis", "Cutaneous Indeterminate Dendritic Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous Indeterminate Dendritic Cell Tumor", "shortest_name_length": 42}
{"curie": "MONDO:0002718", "names": ["CNS teratoma", "CNS Teratoma", "Teratoma of CNS", "teratoma of CNS", "teratoma of the CNS", "Teratoma of the CNS", "Central Nervous System Teratoma", "central nervous system teratoma", "Teratoma of Central Nervous System", "teratoma of central nervous system", "Teratoma of the Central Nervous System", "teratoma of the central nervous system", "Teratoma of the central nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system teratoma", "shortest_name_length": 12}
{"curie": "MONDO:0012597", "names": ["HPC9", "Prostate Cancer, Hereditary, 9", "PROSTATE CANCER, HEREDITARY, 9", "prostate cancer, hereditary, 9", "prostate cancer, hereditary, type 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate cancer, hereditary, 9", "shortest_name_length": 4}
{"curie": "UMLS:C1831917", "names": ["Dermatologic Complication", "dermatologic complications"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dermatologic Complication", "shortest_name_length": 25}
{"curie": "MONDO:8000004", "names": ["salmonella discitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "salmonella discitis", "shortest_name_length": 19}
{"curie": "MONDO:0018024", "names": ["hV", "Hydroa Vacciniforme", "HYDROA VACCINIFORME", "hydroa vacciniforme", "Hydroa vacciniforme", "Bazin's hydroa vacciniforme", "Hydroa vacciniforme (disorder)", "Acute vesiculation and crusting and scarring following sun exposure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hydroa vacciniforme", "shortest_name_length": 2}
{"curie": "MONDO:0012100", "names": ["MDD2", "UNIPOLAR DEPRESSION 2", "Unipolar Depression 2", "unipolar depression 2", "Major Depressive Disorder 2", "MAJOR DEPRESSIVE DISORDER 2", "major depressive disorder 2", "major depressive disorder type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "major depressive disorder 2", "shortest_name_length": 4}
{"curie": "MONDO:0015499", "names": ["paralytic facial malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paralytic facial malformation", "shortest_name_length": 29}
{"curie": "UMLS:C1947968", "names": ["Metastatic Skin Cancer", "Metastatic Skin Carcinoma", "Carcinoma Metastatic to the Skin", "Metastatic Carcinoma in the Skin", "Carcinoma Metastatic in the Skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carcinoma Metastatic to the Skin", "shortest_name_length": 22}
{"curie": "UMLS:C5206633", "names": ["Differentiated PeIN", "Differentiated (Simplex) PeIN", "Differentiated Penile Intraepithelial Neoplasia", "Differentiated penile intraepithelial neoplasia", "Differentiated PeIN (penile intraepithelial neoplasia)", "Differentiated (Simplex) Penile Intraepithelial Neoplasia", "Differentiated penile intraepithelial neoplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Differentiated penile intraepithelial neoplasia", "shortest_name_length": 19}
{"curie": "MONDO:0002066", "names": ["BRAME", "Adenomyoepithelioma", "Breast Adenomyoepithelioma", "breast adenomyoepithelioma", "adenomyoepithelioma of the breast", "Adenomyoepithelioma of the Breast", "Adenomyoepithelioma with carcinoma", "Malignant Breast Adenomyoepithelioma", "Malignant Adenomyoepithelioma of Breast", "malignant adenomyoepithelioma of breast", "Malignant Adenomyoepithelioma of the Breast", "breast adenomyoepithelioma with malignant change", "Breast Adenomyoepithelioma with Malignant Change", "breast Adenomyoepithelioma with malignant Change"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast adenomyoepithelioma", "shortest_name_length": 5}
{"curie": "UMLS:C4525436", "names": ["Stage IIIA Ampulla of Vater Cancer", "Stage IIIA Ampulla of Vater Cancer AJCC v8", "Stage IIIA Ampulla of Vater Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Ampulla of Vater Cancer AJCC v8", "shortest_name_length": 34}
{"curie": "UMLS:C5555510", "names": ["Refractory Pseudomyxoma Peritonei"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Pseudomyxoma Peritonei", "shortest_name_length": 33}
{"curie": "MONDO:0008259", "names": ["Psp", "PSP", "spontaneous pneumothorax", "Primary Spontaneous Pneumothorax", "pneumothorax spontaneous primary", "primary spontaneous pneumothorax", "Primary spontaneous pneumothorax", "Pneumothorax, Primary Spontaneous", "Familial spontaneous pneumothorax", "PNEUMOTHORAX, PRIMARY SPONTANEOUS", "familial spontaneous pneumothorax", "pneumothorax, primary spontaneous", "Spontaneous Pneumothorax, Primary", "Primary spontaneous pneumothorax (disorder)", "Familial spontaneous pneumothorax (disorder)", "primary spontaneous pneumothorax (diagnosis)", "[OBSOLETE] Pneumothorax, Primary Spontaneous"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial spontaneous pneumothorax", "shortest_name_length": 3}
{"curie": "UMLS:C4324627", "names": ["Gadolinium deposition disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gadolinium deposition disease", "shortest_name_length": 29}
{"curie": "MONDO:0024275", "names": ["amebiasis", "Amebiasis", "amoebiasis", "colitis amebic", "Amebic colitis", "amebic colitis", "Amebic Colitis", "Amoebic colitis", "Colitis;amoebic", "COLITIS AMOEBIC", "colitis; amebic", "Colitis, Amebic", "amebic; colitis", "Amoebic Colitis", "amoebic colitis", "colitis, amebic", "Amebic Colitides", "colitis, amoebic", "Amebic dysentery", "amebic colitides", "AMEBIC DYSENTERY", "bowel; amebiasis", "amebic dysentery", "amebiasis; bowel", "Amebic Dysentery", "Colitis, Amoebic", "dysentery amebic", "amebic; dysentery", "Amoebic Dysentery", "Colitides, amebic", "amoebic dysentery", "dysentery; amebic", "Dysentery, Amebic", "Amoebic Colitides", "Amoebic dysentery", "amoebic Colitides", "Colitides, Amebic", "Dysentery;amoebic", "amebic dysenteries", "Colitides, Amoebic", "Colitides, amoebic", "dysentery, amoebic", "Dysentery, Amoebic", "Amebic Dysenteries", "Dysenteries, Amebic", "Amoebic Dysenteries", "dysenteries, amebic", "amoebic dysenteries", "intestinal amebiasis", "Dysenteries, Amoebic", "Intestinal Amebiases", "intestinal Amebiases", "INTESTINAL AMEBIASIS", "Intestinal amebiasis", "dysenteries, amoebic", "amebiasis intestinal", "Intestinal Amebiasis", "Intestinal Amoebiases", "amebiasis, intestinal", "intestinal Amoebiases", "Amebiasis, Intestinal", "amoebiasis intestinal", "Amebiases, intestinal", "intestinal amoebiasis", "Intestinal Amoebiasis", "Intestinal amoebiasis", "Amebiases, Intestinal", "Amoebiasis, Intestinal", "amoebiases, intestinal", "amoebiasis, intestinal", "Amoebiases, Intestinal", "intestinal Entamoebiases", "intestinal entamoebiasis", "Amebic colitis (disorder)", "entamoebiasis, intestinal", "Entamoebiases, intestinal", "Amebic colitis (diagnosis)", "Amebic dysentery (disorder)", "amebic dysentery (diagnosis)", "amoebiasis due to Entamoeba histolytica", "Intestinal Entamoeba histolytica Infection", "amoebic dysentery due to Entamoeba histolytica"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amebic dysentery", "shortest_name_length": 9}
{"curie": "MONDO:0015316", "names": ["congenital laryngeal palsy", "Congenital laryngeal palsy", "Congenital Vocal Cord Palsy", "Congenital vocal cord palsy", "Vocal Cord Palsy, Congenital", "congenital vocal cord paralysis", "Congenital vocal cord paralysis", "Congenital vocal cord palsy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital laryngeal palsy", "shortest_name_length": 26}
{"curie": "UMLS:C0742224", "names": ["Candida cervicitis", "CERVICITIS CANDIDA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Candida cervicitis", "shortest_name_length": 18}
{"curie": "UMLS:C1518730", "names": ["Ovarian Sertoli-Leydig Cell Tumor with Heterologous Elements"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Sertoli-Leydig Cell Tumor with Heterologous Elements", "shortest_name_length": 60}
{"curie": "MONDO:0017896", "names": ["nonmedullary thyroid cancer", "Thyroid cancer, nonmedullary", "thyroid cancer, nonmedullary", "Nonmedullary thyroid carcinoma", "Nonmedullary Thyroid Carcinoma", "Thyroid Carcinoma, Nonmedullary", "Carcinoma, Nonmedullary Thyroid", "Non-medullary thyroid carcinoma", "Nonmedullary Thyroid Carcinomas", "Carcinomas, Nonmedullary Thyroid", "Thyroid Carcinomas, Nonmedullary", "thyroid gland nonmedullary carcinoma", "familial nonmedullary thyroid carcinoma", "NONMEDULLARY THYROID CARCINOMA, PAPILLARY", "Nonmedullary thyroid carcinoma (papillary)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial nonmedullary thyroid carcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0021480", "names": ["benign soft palate tumor", "Benign Soft Palate Tumor", "benign soft palate neoplasm", "Benign Tumor of Soft Palate", "Benign Soft Palate Neoplasm", "soft palate benign neoplasm", "benign tumor of soft palate", "Benign tumor of soft palate", "Benign tumour of soft palate", "Benign neoplasm of soft palate", "Benign Neoplasm of Soft Palate", "benign neoplasm of soft palate", "Benign Tumor of the Soft Palate", "benign tumor of the soft palate", "benign neoplasm of the soft palate", "Benign Neoplasm of the Soft Palate", "Benign neoplasm of the soft palate", "Benign neoplasm of soft palate (disorder)", "benign neoplasm of soft palate (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of soft palate", "shortest_name_length": 24}
{"curie": "MONDO:0024558", "names": ["Rusat", "RUSAT1", "thrombocytopenia, congenital, with radioulnar synostosis", "RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 1", "radioulnar synostosis with amegakaryocytic thrombocytopenia 1", "HOXA11 radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome", "radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome caused by mutation in HOXA11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radioulnar synostosis with amegakaryocytic thrombocytopenia 1", "shortest_name_length": 5}
{"curie": "UMLS:C3272811", "names": ["Rectal Serrated Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rectal Serrated Adenocarcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0044205", "names": ["SDS2", "Shwachman-Diamond syndrome 2", "SHWACHMAN-DIAMOND SYNDROME 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Shwachman-Diamond syndrome 2", "shortest_name_length": 4}
{"curie": "MONDO:0016380", "names": ["Malignant down", "hypertrichosis lanuginosa", "Hypertrichosis lanuginosa", "lanuginosa; hypertrichosis", "hypertrichosis; lanuginosa", "Acquired hypertrichosis lanuginosa", "acquired hypertrichosis lanuginosa", "hypertrichosis lanuginosa, acquired", "Hypertrichosis lanuginosa, acquired", "Hypertrichosis lanuginosa (disorder)", "hypertrichosis; lanuginosa, acquired", "hypertrichosis lanuginosa (diagnosis)", "Acquired hypertrichosis lanuginosa (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired hypertrichosis lanuginosa", "shortest_name_length": 14}
{"curie": "MONDO:0016307", "names": ["Niemann-Pick disease type C, severe early infantile neurologic onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Niemann-Pick disease type C, severe early infantile neurologic onset", "shortest_name_length": 68}
{"curie": "UMLS:C4527004", "names": ["Stage I Retroperitoneal Sarcoma", "Stage I Retroperitoneal Sarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Retroperitoneal Sarcoma AJCC v8", "shortest_name_length": 31}
{"curie": "MONDO:0100350", "names": ["HMN5", "DHMN5", "dHMN5", "DSMAV", "distal HMN V", "distal spinal muscular atrophy type 5", "distal spinal muscular atrophy type V", "distal hereditary motor neuropathy type V", "distal hereditary motor neuronopathy type 5", "Neuronopathy, Distal Hereditary Motor, Type V", "neuronopathy, distal hereditary motor, type 5", "distal spinal muscular atrophy with upper limb predominance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuronopathy, distal hereditary motor, type 5", "shortest_name_length": 4}
{"curie": "MONDO:0014986", "names": ["FANCR", "RAD51 Fanconi anemia", "Fanconi anemia complementation group R", "Fanconi anemia, complementation GROUP R", "FANCONI ANEMIA, COMPLEMENTATION GROUP R", "Fanconi Anemia, complementation group R", "Fanconi anemia caused by mutation in RAD51", "Fanconi anemia complementation group type R", "Fanconi Anemia, complementation group type R"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fanconi anemia complementation group R", "shortest_name_length": 5}
{"curie": "MONDO:0001373", "names": ["urinary bladder posterior wall cancer", "malignant tumor of posterior wall of bladder", "malignant neoplasm of posterior wall of bladder", "Malignant neoplasm of posterior wall of bladder", "malignant neoplasm of posterior wall of urinary bladder", "Malignant neoplasm of posterior wall of urinary bladder", "malignant neoplasm of posterior wall of bladder (diagnosis)", "Malignant neoplasm of posterior wall of urinary bladder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urinary bladder posterior wall cancer", "shortest_name_length": 37}
{"curie": "UMLS:C1336263", "names": ["Ovarian Yolk Sac Tumor Stage III", "Stage III Ovarian Yolk Sac Tumor", "Yolk Sac Tumor of Ovary Stage III", "Yolk Sac Tumor of the Ovary Stage III", "Stage III Ovarian Yolk Sac Tumor AJCC v7", "Stage III Ovarian Yolk Sac Tumor AJCC v6", "Stage III Ovarian Yolk Sac Tumor AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Ovarian Yolk Sac Tumor AJCC v6 and v7", "shortest_name_length": 32}
{"curie": "UMLS:C0151601", "names": ["conjunctiva; edema", "CONJUNCTIVAL EDEMA", "edema; conjunctiva", "Conjunctival edema", "Edema conjunctival", "EDEMA CONJUNCTIVAL", "Oedema conjunctival", "Conjunctival oedema", "CONJUNCTIVAL OEDEMA", "Edema of conjunctiva", "Oedema of conjunctiva", "Conjunctival edema (disorder)", "Conjunctival edema (diagnosis)", "conjunctival vascular disorder edema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conjunctival edema", "shortest_name_length": 18}
{"curie": "UMLS:C5555532", "names": ["Refractory Lung Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Lung Adenocarcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0021218", "names": ["placenta tumor", "Placenta Tumor", "placental tumor", "placenta tumors", "Placental Tumor", "Placenta Tumors", "placental tumors", "Placental Tumors", "Placenta Neoplasm", "placenta neoplasm", "tumor of placenta", "Tumor of Placenta", "Placenta Neoplasms", "placenta neoplasms", "Placental Neoplasm", "placental neoplasm", "Neoplasm of Placenta", "neoplasm of placenta", "Tumor of the Placenta", "tumor of the placenta", "Neoplasm of the Placenta", "neoplasm of the placenta", "placenta neoplasm (disease)", "trophoblastic tumor placental site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "placenta neoplasm", "shortest_name_length": 14}
{"curie": "MONDO:0009167", "names": ["Bonnemann-Meinecke-Reich syndrome", "Bonnemann Meinecke Reich syndrome", "encephalopathy-intracerebral calcification-retinal degeneration syndrome", "Encephalopathy-intracerebral calcification-retinal degeneration syndrome", "Encephalopathy, intracerebral calcification, retinal degeneration syndrome", "encephalopathy, intracerebral calcification, retinal degeneration syndrome", "Encephalopathy, intracerebral calcification, retinal degeneration syndrome (disorder)", "encephalopathy, intracerebral calcification, retinal degeneration syndrome (diagnosis)", "encephalopathy intracranial calcification growth hormone deficiency microcephaly retinal degeneration", "encephalopathy with intracranial calcification, growth hormone deficiency, microcephaly, and retinal degeneration", "ENCEPHALOPATHY WITH INTRACRANIAL CALCIFICATION, GROWTH HORMONE DEFICIENCY, MICROCEPHALY, AND RETINAL DEGENERATION", "Encephalopathy with Intracranial Calcification, Growth Hormone Deficiency, Microcephaly, and Retinal Degeneration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bonnemann-Meinecke-Reich syndrome", "shortest_name_length": 33}
{"curie": "MONDO:0009629", "names": ["DBQD1", "desbuquois syndrome", "DESBUQUOIS DYSPLASIA 1", "Desbuquois dysplasia 1", "CANT1 Desbuquois dysplasia", "Desbuquois dysplasia type 1", "DESBUQUOIS DYSPLASIA, KIM VARIANT", "Desbuquois dysplasia, Kim variant", "Desbuquois dysplasia caused by mutation in CANT1", "micromelic dwarfism with vertebral and metaphyseal abnormalities and advanced carpotarsal ossification"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Desbuquois dysplasia 1", "shortest_name_length": 5}
{"curie": "MONDO:0044887", "names": ["central nervous system non-Hodgkin lymphoma", "Central Nervous System Non-Hodgkin Lymphoma", "Central nervous system non-Hodgkin lymphoma", "central nervous system non-hodgkin lymphoma", "non-Hodgkin lymphoma of central nervous system", "Non-Hodgkin lymphoma of central nervous system", "Non-Hodgkin's lymphoma of central nervous system", "non-Hodgkin's lymphoma of central nervous system", "Primary Central Nervous System Non-Hodgkin Lymphoma", "primary central nervous system non-Hodgkin lymphoma", "Primary Central nervous system non-Hodgkin lymphoma", "central nervous system malignant lymphoma non-Hodgkin's", "Non-Hodgkin's lymphoma of central nervous system (disorder)", "non-Hodgkin's lymphoma of central nervous system (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system non-hodgkin lymphoma", "shortest_name_length": 43}
{"curie": "MONDO:0017052", "names": ["Intermediate MSUD", "Intermediate BCKD deficiency", "intermediate maple syrup urine disease", "Intermediate branched-chain 2-ketoacid dehydrogenase deficiency", "Intermediate branched-chain alpha-ketoacid dehydrogenase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intermediate maple syrup urine disease", "shortest_name_length": 17}
{"curie": "UMLS:C4684950", "names": ["Inoperable Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Inoperable Disease", "shortest_name_length": 18}
{"curie": "MONDO:0100414", "names": ["AML, CEBPA Mutation", "AML, CEBP Gene Mutation", "AML, CEBPA gene mutation", "AML, C/EBPalpha Mutation", "AML, C/EBP-Alpha Gene Mutation", "Familial Acute Myeloid Leukaemia", "acute myeloid leukemia, CEBPA gene mutation", "Cebpa-Dependent Familial Acute Myeloid Leukemia", "Familial Acute Myeloid Leukemia with Mutated CEBPA", "Familial Acute Myeloid Leukemia with Mutated Cebpa", "Acute Myeloid Leukemia with Germline CEBPA Mutation", "AML, CCAAT Enhancer Binding Protein Alpha Gene Mutation", "AML, CCAAT/Enhancer Binding Protein, Alpha Gene Mutation", "Acute Myeloid Leukemia with Germline Biallelic CEBPA Mutations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, CEBPA gene mutation", "shortest_name_length": 19}
{"curie": "UMLS:C4055247", "names": ["Childhood MALToma", "Childhood MALT Lymphoma", "Childhood Extranodal Marginal Zone Lymphoma of MALT", "Childhood Extranodal Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Extranodal Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue", "shortest_name_length": 17}
{"curie": "MONDO:0021829", "names": ["Plurimalformative syndrome", "agnathia-microstomia-synotia", "Agnathia-microstomia-synotia", "Agnathia, microstomia, synotia and cardiac and pulmonary maldevelopment", "agnathia, microstomia, synotia and cardiac and pulmonary maldevelopment"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "agnathia-microstomia-synotia", "shortest_name_length": 26}
{"curie": "MONDO:0003244", "names": ["CNS Soft Tissue Tumor", "CNS soft tissue tumor", "soft tissue tumor of CNS", "CNS Soft Tissue Neoplasm", "CNS soft tissue neoplasm", "Soft Tissue Tumor of CNS", "Soft Tissue Neoplasm of CNS", "soft tissue neoplasm of CNS", "Soft Tissue Tumor of the CNS", "soft tissue tumor of the CNS", "soft tissue neoplasm of the CNS", "Soft Tissue Neoplasm of the CNS", "Non-meningothelial mesenchymal tumor", "non-meningothelial mesenchymal tumor", "Non-meningothelial mesenchymal tumour", "Central Nervous System Soft Tissue Tumor", "central nervous system soft tissue tumor", "Central Nervous System Soft Tissue Neoplasm", "central nervous system soft tissue neoplasm", "Soft Tissue Tumor of Central Nervous System", "soft tissue tumor of central nervous system", "Mesenchymal, Non-Meningothelial Tumor of CNS", "mesenchymal, non-meningothelial tumor of CNS", "soft tissue neoplasm of central nervous system", "Soft Tissue Neoplasm of Central Nervous System", "Soft Tissue Tumor of the Central Nervous System", "soft tissue tumor of the central nervous system", "mesenchymal, non-meningothelial tumor of the CNS", "Mesenchymal, Non-Meningothelial Tumor of the CNS", "Soft Tissue Neoplasm of the Central Nervous System", "soft tissue neoplasm of the central nervous system", "central nervous system mesenchymal non-meningothelial tumor", "Central Nervous System Mesenchymal, Non-Meningothelial Tumor", "central nervous system mesenchymal, non-meningothelial tumor", "central nervous system mesenchymal non-meningothelial tumour", "Mesenchymal, Non-Meningothelial Tumor of Central Nervous System", "Central Nervous System Mesenchymal, Non-Meningothelial Neoplasm", "central nervous system mesenchymal, non-meningothelial neoplasm", "mesenchymal, non-meningothelial tumor of central nervous system", "Mesenchymal Non-Meningothelial Tumor of the Central Nervous System", "mesenchymal non-meningothelial tumor of the central nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system mesenchymal non-meningothelial tumor", "shortest_name_length": 21}
{"curie": "UMLS:C5239290", "names": ["Cutaneous Rosai-Dorfman Disease", "Cutaneous Sinus Histiocytosis With Massive Lymphadenopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous Rosai-Dorfman Disease", "shortest_name_length": 31}
{"curie": "UMLS:C5420822", "names": ["Refractory Vaginal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Vaginal Carcinoma", "shortest_name_length": 28}
{"curie": "UMLS:C0341353", "names": ["Appendix Mass", "Appendix mass", "Appendiceal Mass", "Mass of appendix", "Mass of appendix (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Appendix mass", "shortest_name_length": 13}
{"curie": "MONDO:0021324", "names": ["abdominal part of esophagus cancer", "cancer of abdominal part of esophagus", "malignant tumor of abdominal esophagus", "Malignant Tumor of Abdominal Esophagus", "malignant neoplasm of abdominal esophagus", "Malignant Neoplasm of Abdominal Esophagus", "Malignant neoplasm of abdominal esophagus", "Malignant Tumor of the Abdominal Esophagus", "Malignant neoplasm of abdominal oesophagus", "malignant tumor of the abdominal esophagus", "Malignant Neoplasm of the Abdominal Esophagus", "malignant neoplasm of the abdominal esophagus", "malignant abdominal part of esophagus neoplasm", "Malignant tumor of abdominal part of esophagus", "Malignant tumour of abdominal part of oesophagus", "Malignant neoplasm of abdominal part of esophagus", "malignant neoplasm of abdominal part of esophagus", "Malignant neoplasm of abdominal part of oesophagus", "malignant neoplasm of abdominal esophagus (diagnosis)", "Malignant tumor of abdominal part of esophagus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant neoplasm of abdominal esophagus", "shortest_name_length": 34}
{"curie": "MONDO:0014176", "names": ["IHPRF", "IHPRF syndrome", "hypotonia-speech impairment-severe cognitive delay syndrome", "infantile hypotonia-psychomotor retardation-characteristic facies syndrome", "hypotonia, infantile, with psychomotor retardation and characteristic facies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotonia, infantile, with psychomotor retardation and characteristic facies", "shortest_name_length": 5}
{"curie": "UMLS:C5206773", "names": ["Refractory Epithelioid Malignant Peripheral Nerve Sheath Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Epithelioid Malignant Peripheral Nerve Sheath Tumor", "shortest_name_length": 62}
{"curie": "MONDO:0006516", "names": ["Sarcopenia", "sarcopenia", "Sarcopenias", "Sarcopenia (disorder)", "sarcopenia (diagnosis)", "Loss of skeletal muscle mass"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sarcopenia", "shortest_name_length": 10}
{"curie": "UMLS:C0278727", "names": ["recurrent SCLC", "SCLC, recurrent", "oat cell lung cancer, recurrent", "Relapsed Small Cell Lung Cancer", "Recurrent Small Cell Lung Cancer", "recurrent small cell lung cancer", "Small cell lung cancer recurrent", "small cell lung cancer, recurrent", "lung cancer, recurrent small cell", "Relapsed Small Cell Lung Carcinoma", "Recurrent Small Cell Lung Carcinoma", "Recurrent Lung Small Cell Carcinoma", "Relapsed Small Cell Carcinoma of Lung", "Recurrent Small Cell Carcinoma of Lung", "Relapsed Small Cell Carcinoma of the Lung", "Recurrent Small Cell Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small cell lung cancer recurrent", "shortest_name_length": 14}
{"curie": "UMLS:C1336130", "names": ["Stage IB Adenosquamous Lung Cancer", "Stage IB Adenosquamous Lung Carcinoma", "Stage IB Adenosquamous Cell Lung Carcinoma", "Stage IB Lung Adenosquamous Carcinoma AJCC v7", "Stage IB Adenosquamous Cell Carcinoma of Lung", "Stage IB Adenosquamous Cell Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Lung Adenosquamous Carcinoma AJCC v7", "shortest_name_length": 34}
{"curie": "UMLS:C4763840", "names": ["Metastatic Clear Cell Urothelial Carcinoma", "Metastatic Clear Cell Bladder Urothelial Carcinoma", "Metastatic Clear Cell Urothelial Carcinoma of the Bladder", "Metastatic Infiltrating Bladder Urothelial Carcinoma, Clear Cell Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Infiltrating Bladder Urothelial Carcinoma, Clear Cell Variant", "shortest_name_length": 42}
{"curie": "UMLS:C4528559", "names": ["Stage IIIB Breast Cancer", "Anatomic Stage IIIB Breast Cancer AJCC v8", "Anatomic Stage IIIB Breast Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anatomic Stage IIIB Breast Cancer AJCC v8", "shortest_name_length": 24}
{"curie": "MONDO:0009152", "names": ["ECTOL2", "autosomal recessive isolated ectopia lentis", "ectopia lentis, isolated autosomal recessive", "ectopia lentis, isolated, autosomal recessive", "autosomal recessive isolated ectopia lentis 2", "ectopia lentis 2, isolated, autosomal recessive", "ECTOPIA LENTIS 2, ISOLATED, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectopia lentis 2, isolated, autosomal recessive", "shortest_name_length": 6}
{"curie": "MONDO:0005252", "names": ["heart failure", "Heart Failure", "Heart failure", "failure, heart", "cardiac failure", "Cardiac Failure", "myocardial failure", "Failure;myocardial", "Myocardial failure", "Myocardial Failure", "failure; myocardial", "myocardium; failure", "myocardium; weakness", "cardiac insufficiency", "insufficiency, Cardiac", "Myocardial failure NOS", "myocardium; insufficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heart failure", "shortest_name_length": 13}
{"curie": "MONDO:0006176", "names": ["cribriform carcinoma", "Cribriform carcinoma", "Cribriform Carcinoma", "Cribriform Carcinomas", "Carcinoma, Cribriform", "Carcinomas, Cribriform", "Cribriform carcinoma, NOS", "cribriform carcinoma (diagnosis)", "Ductal carcinoma, cribriform type", "Cribriform carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cribriform carcinoma", "shortest_name_length": 20}
{"curie": "MONDO:0024560", "names": ["PDA", "PDA1", "patent ductus arteriosus 1", "PATENT DUCTUS ARTERIOSUS 1", "patent ductus arteriosus, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PDA1", "shortest_name_length": 3}
{"curie": "UMLS:C1112503", "names": ["Colon Tubular Adenoma", "Colonic tubular adenoma", "Tubular adenoma of colon", "Tubular adenoma of colon (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tubular adenoma of colon", "shortest_name_length": 21}
{"curie": "UMLS:C0406317", "names": ["Plaque psoriasis", "plaque psoriasis", "psoriasis; plaque", "Discoid psoriasis", "Nummular psoriasis", "nummular; psoriasis", "psoriasis; nummular", "en plaques; psoriasis", "Plaque psoriasis (disorder)", "plaque psoriasis (diagnosis)", "Chronic small plaque psoriasis", "chronic small plaque psoriasis", "Chronic small plaque psoriasis (disorder)", "chronic small plaque psoriasis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic small plaque psoriasis", "shortest_name_length": 16}
{"curie": "MONDO:0017279", "names": ["YOPD", "young onset Parkinson disease", "Early onset Parkinson disease", "young-onset Parkinson disease", "Parkinson disease young onset", "Young-onset Parkinson disease", "Young onset Parkinson disease", "Early-onset Parkinson disease", "early-onset Parkinson disease", "Young onset Parkinson's disease", "Early onset Parkinson's disease", "early-onset Parkinson's disease", "Young onset Parkinson disease (disorder)", "young onset Parkinson disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "young-onset Parkinson disease", "shortest_name_length": 4}
{"curie": "UMLS:C1512194", "names": ["Gliomatosis Cerebri Type II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gliomatosis Cerebri Type II", "shortest_name_length": 27}
{"curie": "MONDO:0020327", "names": ["classic Hodgkin lymphoma, nodular sclerosis type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "classic Hodgkin lymphoma, nodular sclerosis type", "shortest_name_length": 48}
{"curie": "UMLS:C4527070", "names": ["stage IIB Merkel cell carcinoma", "pathologic stage IIB Merkel cell carcinoma AJCC v8", "Pathologic Stage IIB Merkel Cell Carcinoma AJCC v8", "pathologic stage IIB neuroendocrine carcinoma of the skin AJCC v8", "Pathologic Stage IIB Neuroendocrine Carcinoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IIB Merkel Cell Carcinoma AJCC v8", "shortest_name_length": 31}
{"curie": "MONDO:0015271", "names": ["Bent spine", "bent spine", "Camptospasm", "camptospasm", "Camptocormia", "camptocormia", "camptocormism", "Camptocormism", "Bent spine syndrome", "Bent Spine Syndrome", "bent spine syndrome", "Camptocormia (disorder)", "idiopathic camptocormia", "Idiopathic camptocormia", "Idiopathic camptocormism", "idiopathic camptocormism", "Idiopathic progressive lumbar kyphosis", "idiopathic progressive lumbar kyphosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic camptocormia", "shortest_name_length": 10}
{"curie": "MONDO:0035027", "names": ["microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome", "shortest_name_length": 87}
{"curie": "UMLS:C0751623", "names": ["second cancer", "cancer second", "Second Cancer", "Cancer, Second", "Second Cancers", "second cancers", "Cancers, Second", "Second primary cancer", "second primary cancer", "Second Primary Cancer", "Second Primary Cancers", "Cancer, Second Primary", "Cancers, Second Primary", "Second primary malignancy", "secondary malignant neoplasm", "Second primary cancer (disorder)", "Second Primary Malignant Neoplasm", "secondary malignant neoplasm (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Second Primary Cancers", "shortest_name_length": 13}
{"curie": "MONDO:0013571", "names": ["Takahara", "acatalasia", "ACATALASIA", "Acatalasia", "Acatalasemia", "acatalasemia", "ACATALASEMIA", "Acatalasaemia", "Takahara disease", "Takahara Disease", "Takaharas Disease", "Disease, Takahara", "Takahara's Disease", "Catalase Deficiency", "Catalase deficiency", "Disease, Takahara's", "catalase deficiency", "Takahara's syndrome", "CATALASE DEFICIENCY", "Deficiency, Catalase", "Catalase Deficiencies", "Deficiencies, Catalase", "deficiency of catalase", "Deficiency of catalase", "Acatalasemia (disorder)", "Acatalasemia (diagnosis)", "Deficiency of catalase (disorder)", "defects of catalase and peroxidase acatalasemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acatalasia", "shortest_name_length": 8}
{"curie": "MONDO:0011634", "names": ["RMD", "RIPPLING MUSCLE DISEASE", "Rippling muscle disease", "rippling muscle disease", "Rippling muscle syndrome", "Rippling muscle disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rippling muscle disease", "shortest_name_length": 3}
{"curie": "UMLS:C2984090", "names": ["Rectosigmoid Cancer by AJCC v7 Stage", "Rectosigmoid Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rectosigmoid Cancer by AJCC v7 Stage", "shortest_name_length": 36}
{"curie": "MONDO:0025354", "names": ["SPGFX3", "X-linked spermatogenic failure 3", "SPERMATOGENIC FAILURE, X-LINKED, 3", "spermatogenic failure, X-linked, 3", "spermatogenic failure, X-linked, 3, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure, X-linked, 3", "shortest_name_length": 6}
{"curie": "MONDO:0018692", "names": ["Variably protease sensitive prionopathy", "Variably protease-sensitive prionopathy", "variably protease-sensitive prionopathy", "Variably protease sensitive prionopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "variably protease-sensitive prionopathy", "shortest_name_length": 39}
{"curie": "UMLS:C0456127", "names": ["Osteopenic rickets", "osteopenia prematurity", "Osteopenia of prematurity", "osteopenia of prematurity", "osteopenia prematurity (diagnosis)", "Osteopenia of prematurity (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Osteopenia of prematurity", "shortest_name_length": 18}
{"curie": "MONDO:0017951", "names": ["TRPS", "trichorhinophalangeal syndrome", "Trichorhinophalangeal syndrome", "Trichorhinophalangeal syndrome (disorder)", "Trichorhinophalangeal syndrome (diagnosis)", "multiple malformation syndrome trichorhinophalangeal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichorhinophalangeal syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C2987195", "names": ["Pancreatic Intraductal Papillary Mucinous Neoplasm, Pancreatobiliary-Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Intraductal Papillary Mucinous Neoplasm, Pancreatobiliary-Type", "shortest_name_length": 73}
{"curie": "UMLS:C0269874", "names": ["Third degree perineal tear", "Third degree perineal laceration", "Third Degree Perineal Laceration", "perineal rupture, obstetric; anus", "anus; perineal rupture, obstetric", "Obstetrical laceration, third degree", "Third degree perineal laceration, NOS", "Laceration, obstetrical, third degree", "laceration; anus, complicating delivery", "perineal rupture, obstetric; third degree", "Third degree perineal tear during delivery", "Third degree perineal laceration (disorder)", "Third-degree perineal laceration, with delivery", "third-degree perineal laceration during delivery", "Third-degree perineal laceration during delivery", "laceration; sphincter ani, complicating delivery", "Third degree perineal laceration during delivery", "Third degree perineal laceration (physical finding)", "laceration; perineum, third degree, complicating delivery", "post-delivery exam showing third degree perineal laceration", "third-degree perineal laceration during delivery (diagnosis)", "post-delivery exam showing third degree laceration of perineum", "post-delivery exam showing third degree laceration of perineum (physical finding)", "Laceration of tissues between vaginal and perineal muscular layers and rectal mucosa", "Laceration of tissues between vaginal AND/OR perineal muscular layers and rectal mucosa", "Third-degree perineal laceration, delivered, with or without mention of antepartum condition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Third degree perineal laceration", "shortest_name_length": 26}
{"curie": "UMLS:C4521610", "names": ["Stage III Pleural Malignant Mesothelioma", "Stage III Pleural Malignant Mesothelioma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Pleural Malignant Mesothelioma AJCC v8", "shortest_name_length": 40}
{"curie": "MONDO:0015622", "names": ["Wound myiasis", "wound myiasis", "myiasis; wound", "wound; myiasis", "traumatic myiasis", "Traumatic myiasis", "traumatic; myiasis", "myiasis; traumatic", "Infestation of wound caused by fly larvae", "Infestation of wound caused by fly larvae (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "wound myiasis", "shortest_name_length": 13}
{"curie": "MONDO:0001505", "names": ["alcohol hepatitis", "hepatitis alcohol", "ethanol; hepatitis", "alcohol; hepatitis", "hepatitis; ethanol", "Hepatitis;alcoholic", "ALCOHOLIC HEPATITIS", "alcoholic Hepatitis", "HEPATITIS ALCOHOLIC", "alcoholic hepatitis", "Hepatitis alcoholic", "Alcoholic hepatitis", "hepatitis alcoholic", "Alcoholic Hepatitis", "Hepatitis, Alcoholic", "HEPATITIS, ALCOHOLIC", "alcoholics hepatitis", "hepatitis; alcoholic", "AH - Alcoholic hepatitis", "Acute alcoholic hepatitis", "acute alcoholic hepatitis", "Acute Alcoholic Hepatitis", "acute alcoholic Hepatitis", "hepatitis; acute, alcoholic", "acute; hepatitis, alcoholic", "acute alcoholic liver disease", "Acute alcoholic liver disease", "alcoholic liver disease acute", "Alcoholic hepatitis (disorder)", "alcoholic hepatitis (diagnosis)", "Acute alcoholic liver disease (disorder)", "Acute alcoholic liver disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alcoholic hepatitis", "shortest_name_length": 17}
{"curie": "UMLS:C0280308", "names": ["Lower Gum Verrucous Carcinoma", "Verrucous Carcinoma of Lower Gum", "Lower Gingival Verrucous Carcinoma", "Verrucous Carcinoma of Lower Gingiva", "Verrucous Carcinoma of the Lower Gum", "Verrucous Carcinoma of the Lower Gingiva"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lower Gingival Verrucous Carcinoma", "shortest_name_length": 29}
{"curie": "UMLS:C1390484", "names": ["Skull hypoplasia", "hypoplasia; skull", "skull; hypoplasia", "hypoplasia; bone, skull)", "bone; hypoplasia, skull)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skull hypoplasia", "shortest_name_length": 16}
{"curie": "MONDO:0022846", "names": ["congenital nonhemolytic jaundice"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital nonhemolytic jaundice", "shortest_name_length": 32}
{"curie": "UMLS:C1708747", "names": ["LAMN", "Low-Grade Appendix Mucinous Neoplasm", "Low Grade Appendix Mucinous Neoplasm", "Low Grade Appendiceal Mucinous Neoplasm", "Low grade appendiceal mucinous neoplasm", "Low-Grade Appendiceal Mucinous Neoplasm", "low-grade appendiceal mucinous neoplasm (LAMN)", "Appendix Well Differentiated Mucinous Adenocarcinoma", "appendiceal neoplasm malignant low-grade mucinous (LAMN)", "low-grade appendiceal mucinous neoplasm (LAMN) (diagnosis)", "Low grade appendiceal mucinous neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low grade appendiceal mucinous neoplasm", "shortest_name_length": 4}
{"curie": "UMLS:C0685110", "names": ["heart metastases", "heart metastasis", "Metastases to heart", "Metastases to Heart", "Metastasis to Heart", "Metastasis to heart", "Metastases to the Heart", "Metastasis to the Heart", "Cancer metastatic to heart", "CARDIAC NEOPLASM SECONDARY", "CARDIAC NEOPLASM, SECONDARY", "Metastatic Tumor to the Heart", "Metastatic Neoplasm to the Heart", "Secondary malignant tumor of heart", "Secondary malignant tumour of heart", "secondary malignant neoplasm of heart", "Secondary malignant neoplasm of heart", "Metastatic malignant neoplasm to heart", "Metastatic malignant neoplasm of heart", "Metastatic Malignant Neoplasm to the Heart", "Secondary malignant neoplasm of heart, NOS", "Metastatic Malignant Neoplasm in the Heart", "Metastatic malignant neoplasm to heart, NOS", "malignant cardiac neoplasm of heart secondary", "Metastatic malignant neoplasm to heart (disorder)", "Secondary malignant neoplasm of heart (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to heart", "shortest_name_length": 16}
{"curie": "UMLS:C4329634", "names": ["Central Nervous System Langerhans Cell Histiocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Langerhans Cell Histiocytosis", "shortest_name_length": 52}
{"curie": "UMLS:C4763835", "names": ["Bladder Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder Neuroendocrine Neoplasm", "shortest_name_length": 31}
{"curie": "MONDO:0015230", "names": ["Cassia Stocco dos Santos syndrome", "anophthalmia megalocornea cardiopathy skeletal anomalies", "Anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome", "anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome", "Anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome", "Anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome", "shortest_name_length": 33}
{"curie": "MONDO:0043108", "names": ["infantile striato thalamic degeneration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile striato thalamic degeneration", "shortest_name_length": 39}
{"curie": "UMLS:C4683427", "names": ["Thyroid Gland Follicular Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Follicular Carcinoma by AJCC v8 Stage", "shortest_name_length": 51}
{"curie": "MONDO:0003252", "names": ["granular cell cancer", "Myoblastoma, Malignant", "myoblastoma, malignant", "malignant granular cell tumor", "Malignant granular cell tumor", "Malignant Granular Cell Tumor", "GRANULAR CELL TUMOR, MALIGNANT", "Granular cell tumor, malignant", "granular cell tumor, malignant", "Malignant granular cell tumour", "Granular cell tumour, malignant", "malignant granular cell neoplasm", "Malignant Granular Cell Neoplasm", "Malignant granular cell myoblastoma", "Malignant Granular Cell Myoblastoma", "malignant granular cell myoblastoma", "Granular cell myoblastoma, malignant", "Malignant granular cell tumor (disorder)", "malignant granular cell neoplasm (diagnosis)", "neoplasm of nerve sheath origin malignant granular cell", "Granular cell tumor, malignant (morphologic abnormality)", "granular cell tumor, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "granular cell cancer", "shortest_name_length": 20}
{"curie": "UMLS:C0341164", "names": ["Ulcer bleeding gastric", "GASTRIC ULCER BLEEDING", "Bleeding gastric ulcer", "Gastric ulcer bleeding", "bleeding gastric ulcer", "ULCER BLEEDING GASTRIC", "Gastric ulcer hemorrhage", "STOMACH ULCER HEMORRHAGE", "gastric ulcer hemorrhage", "Stomach ulcer hemorrhage", "GASTRIC ULCER HEMORRHAGIC", "Stomach ulcer haemorrhage", "Gastric ulcer hemorrhagic", "Gastric ulcer haemorrhage", "GASTRIC ULCER HAEMORRHAGIC", "Gastric ulcer haemorrhagic", "Gastric ulcer with hemorrhage", "Stomach ulcer with hemorrhage", "Ulcer stomach with hemorrhage", "ULCER STOMACH WITH HEMORRHAGE", "Stomach ulcer with haemorrhage", "Gastric ulcer with haemorrhage", "Ulcer stomach with haemorrhage", "stomach; ulcer, with hemorrhage", "ulcer; gastric, with hemorrhage", "Gastric ulcer, NOS with hemorrhage", "Bleeding gastric ulcer (diagnosis)", "Gastric ulcer, NOS with haemorrhage", "Gastric ulcer with hemorrhage (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bleeding gastric ulcer", "shortest_name_length": 22}
{"curie": "MONDO:0016871", "names": ["partial deletion of chromosome 6", "partial monosomy of chromosome 6", "partial deletion of chromosome type 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of chromosome 6", "shortest_name_length": 32}
{"curie": "MONDO:0006817", "names": ["PAOS", "Parosteal", "Parosteal osteosarcoma", "parosteal osteosarcoma", "Parosteal Osteosarcoma", "parosteal; osteosarcoma", "osteosarcoma; parosteal", "periosteal osteosarcoma", "osteosarcomas periosteal", "Juxtacortical Osteosarcoma", "juxtacortical osteosarcoma", "Juxtacortical osteosarcoma", "osteosarcoma; juxtacortical", "juxtacortical; osteosarcoma", "Osteosarcoma, Juxtacortical", "Juxtacortical Osteosarcomas", "Osteosarcomas, Juxtacortical", "parosteal osteogenic sarcoma", "Parosteal Osteogenic sarcoma", "Parosteal Osteogenic Sarcoma", "juxtacortical osteogenic sarcoma", "Juxtacortical osteogenic sarcoma", "Juxtacortical Osteogenic Sarcoma", "juxtacortical osteosarcoma (diagnosis)", "Parosteal osteosarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juxtacortical osteosarcoma", "shortest_name_length": 4}
{"curie": "UMLS:C5420227", "names": ["Oral Cavity Soft Tissue Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral Cavity Soft Tissue Sarcoma", "shortest_name_length": 31}
{"curie": "MONDO:0018724", "names": ["X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome", "shortest_name_length": 93}
{"curie": "MONDO:0018840", "names": ["isolated CHF", "congenital fibrose liver", "Congenital Fibrose Liver", "Congenital liver fibrosis", "congenital liver fibrosis", "congenital fibrosis liver", "CONGENITAL HEPATIC FIBROSIS", "congenital hepatic fibrosis", "Congenital hepatic fibrosis", "Congenital Hepatic Fibrosis", "Hepatic Fibrosis, Congenital", "Hepatic fibrosis, congenital", "HEPATIC FIBROSIS, CONGENITAL", "isolated congenital hepatic fibrosis", "Congenital hepatic fibrosis (disorder)", "congenital hepatic fibrosis (diagnosis)", "nonsyndromic congenital hepatic fibrosis", "Excessive buildup of connective tissue and scarring of liver at birth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated congenital hepatic fibrosis", "shortest_name_length": 12}
{"curie": "MONDO:0016223", "names": ["infantile hemangioma of rare localization", "Infantile hemangioma of rare localization", "Infantile haemangioma of rare localisation", "Infantile hemangioma of rare localization (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile hemangioma of rare localization", "shortest_name_length": 41}
{"curie": "UMLS:C4727078", "names": ["Advanced Synovial Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Synovial Sarcoma", "shortest_name_length": 25}
{"curie": "MONDO:0003744", "names": ["Spindle Cell Uveal Melanoma", "spindle cell uveal melanoma", "uveal spindle cell melanoma", "Uveal spindle cell melanoma", "Uveal Spindle Cell Melanoma", "Spindle Cell Melanoma of Uvea", "spindle cell melanoma of uvea", "spindle cell melanoma of the uvea", "Spindle Cell Intraocular Melanoma", "spindle cell intraocular melanoma", "Spindle Cell Melanoma of the Uvea", "intraocular melanoma, spindle cell", "Intraocular melanoma, spindle cell", "melanoma, spindle cell intraocular", "melanoma, intraocular, spindle cell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spindle cell intraocular melanoma", "shortest_name_length": 27}
{"curie": "MONDO:0032879", "names": ["MGBL", "congenital megabladder", "megabladder, congenital", "MEGABLADDER, CONGENITAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "megabladder, congenital", "shortest_name_length": 4}
{"curie": "UMLS:C1112303", "names": ["Facial wasting", "facial wasting", "temporal wasting"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Facial wasting", "shortest_name_length": 14}
{"curie": "UMLS:C0271036", "names": ["retina scar", "retinal scar", "scar; retina", "Scar, retina", "Retinal Scar", "retina; scar", "Retinal scar", "retinal scars", "retina; cicatrix", "retinal scarring", "Retinal scarring", "Retinal scar, NOS", "Retinal scar (disorder)", "retinal scar (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retinal scar", "shortest_name_length": 11}
{"curie": "MONDO:0022400", "names": ["retinal ciliopathy due to mutation in the RPGRIP gene"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal ciliopathy due to mutation in the RPGRIP gene", "shortest_name_length": 53}
{"curie": "UMLS:C4330503", "names": ["Isolated Non-Pigmented Micronodular Adrenal Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Isolated Non-Pigmented Micronodular Adrenal Hyperplasia", "shortest_name_length": 55}
{"curie": "UMLS:C3640997", "names": ["AIDS-related HPV-related cancer", "AIDS-related HPV-related cancer, NOS", "Human Papillomavirus-Related Malignant Neoplasm in AIDS Patient"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Human Papillomavirus-Related Malignant Neoplasm in AIDS Patient", "shortest_name_length": 31}
{"curie": "MONDO:0013613", "names": ["LCA16", "Leber congenital amaurosis 16", "LEBER CONGENITAL AMAUROSIS 16", "KCNJ13 Leber congenital amaurosis", "Leber congenital amaurosis type 16", "Leber congenital amaurosis caused by mutation in KCNJ13"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leber congenital amaurosis 16", "shortest_name_length": 5}
{"curie": "MONDO:0019112", "names": ["CAR syndrome", "paraneoplastic retinopathy", "Paraneoplastic retinopathy", "cancer-associated retinopathy", "Ocular Paraneoplastic Disease", "Ocular Paraneoplastic Diseases", "Ocular Paraneoplastic Syndrome", "Disease, Ocular Paraneoplastic", "Paraneoplastic Disease, Ocular", "Paraneoplastic Diseases, Ocular", "Syndrome, Ocular Paraneoplastic", "Ocular Paraneoplastic Syndromes", "Paraneoplastic Syndrome, Ocular", "Diseases, Ocular Paraneoplastic", "Syndromes, Ocular Paraneoplastic", "Paraneoplastic Syndromes, Ocular", "Paraneoplastic retinopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cancer-associated retinopathy", "shortest_name_length": 12}
{"curie": "UMLS:C1609536", "names": ["Allergic bronchospasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Allergic bronchospasm", "shortest_name_length": 21}
{"curie": "UMLS:C1335456", "names": ["Posttraumatic Spindle Cell Nodule of Bladder", "Postoperative Spindle Cell Nodule of Bladder", "Posttraumatic Spindle Cell Nodule of the Bladder", "Postoperative Spindle Cell Nodule of the Bladder", "Posttraumatic Spindle Cell Nodule of Urinary Bladder", "Postoperative Spindle Cell Nodule of Urinary Bladder", "Postoperative Spindle Cell Nodule of the Urinary Bladder", "Posttraumatic Spindle Cell Nodule of the Urinary Bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postoperative Spindle Cell Nodule of the Bladder", "shortest_name_length": 44}
{"curie": "MONDO:0012857", "names": ["DSAP3", "POROK5", "porokeratosis 5, disseminated superficial actinic", "porokeratosis, disseminated superficial actinic, 3", "Porokeratosis, Disseminated Superficial Actinic, 3", "POROKERATOSIS, DISSEMINATED SUPERFICIAL ACTINIC, 3", "porokeratosis 5, disseminated superficial actinic type", "POROKERATOSIS 5, DISSEMINATED SUPERFICIAL ACTINIC TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "porokeratosis 5, disseminated superficial actinic type", "shortest_name_length": 5}
{"curie": "MONDO:0060554", "names": ["VCRL1", "3-HYDROXYANTHRANILIC ACIDEMIA", "3-hydroxyanthranilic acidemia", "congenital NAD deficiency Disorder 1", "CONGENITAL NAD DEFICIENCY DISORDER 1", "vertebral, cardiac, renal, and limb defects syndrome 1", "VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vertebral, cardiac, renal, and limb defects syndrome 1", "shortest_name_length": 5}
{"curie": "UMLS:C0856025", "names": ["Stage II Splenic Marginal Zone Lymphoma", "Splenic Marginal Zone Lymphoma Stage II", "Splenic marginal zone lymphoma stage II", "Stage II Splenic Marginal Zone B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Splenic marginal zone lymphoma stage II", "shortest_name_length": 39}
{"curie": "MONDO:0001418", "names": ["Trachea Sarcoma", "trachea sarcoma", "Tracheal Sarcoma", "tracheal sarcoma", "Sarcoma of Trachea", "sarcoma of trachea", "Sarcoma of the Trachea", "sarcoma of the trachea", "sarcoma of trachea (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trachea sarcoma", "shortest_name_length": 15}
{"curie": "MONDO:0011194", "names": ["Ad5", "AD5", "Alzheimer disease-5", "Alzheimer disease 5", "Alzheimer Disease 5", "ALZHEIMER DISEASE 5", "Alzheimer's disease 5", "Alzheimer disease type 5", "Alzheimer's disease type 5", "Alzheimer disease, familial 5", "Alzheimer Disease, Familial, 5", "ALZHEIMER DISEASE, FAMILIAL, 5", "Alzheimer disease, familial, 5", "Alzheimer's disease 5, late onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alzheimer disease 5", "shortest_name_length": 3}
{"curie": "MONDO:0014133", "names": ["DEE16", "EIEE16", "early infantile epileptic encephalopathy 16", "epileptic encephalopathy, early infantile, 16", "developmental and epileptic encephalopathy 16", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 16", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 16", "developmental and epileptic encephalopathy, 16", "epileptic encephalopathy, early infantile, type 16"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 16", "shortest_name_length": 5}
{"curie": "UMLS:C0149966", "names": ["pharynx; gonococcal", "gonococcal; pharynx", "Gonorrhea of pharynx", "Gonorrhoea of pharynx", "gonococcal pharyngitis", "Gonococcal pharyngitis", "pharyngitis gonococcal", "PHARYNGITIS GONOCOCCAL", "pharyngitis; gonococcal", "gonococcal; pharyngitis", "PHARYNGITIS, GONOCOCCAL", "Pharyngeal gonococcal infection", "Gonorrhea of pharynx (disorder)", "Gonococcal infection of pharynx", "gonococcal pharyngitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gonorrhea of pharynx", "shortest_name_length": 19}
{"curie": "UMLS:C3272481", "names": ["Ampulla of Vater Large Cell NEC", "Ampulla of Vater Large Cell Neuroendocrine Carcinoma", "Large Cell Neuroendocrine Carcinoma of the Ampullary Region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ampulla of Vater Large Cell Neuroendocrine Carcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C4331226", "names": ["Recurrent Uterine Corpus Serous Carcinoma", "Recurrent Endometrial Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Endometrial Serous Adenocarcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0011008", "names": ["McPherson-Clemens syndrome", "McPherson Clemens syndrome", "cleft lip/palate-intestinal malrotation-cardiopathy syndrome", "Cleft lip/palate-intestinal malrotation-cardiopathy syndrome", "Cleft lip and cleft palate with intestinal malrotation and cardiopathy syndrome", "Cleft lip and cleft palate with intestinal malrotation and cardiopathy syndrome (disorder)", "CLEFT LIP/PALATE WITH CHARACTERISTIC FACIES, INTESTINAL MALROTATION, AND LETHAL CONGENITAL HEART DISEASE", "cleft LIP/palate with characteristic facies, intestinal malrotation, and lethal congenital heart disease", "Cleft Lip-Palate with Characteristic Facies, Intestinal Malrotation, and Lethal Congenital Heart Disease", "cleft lip, cleft palate, characteristic facies, intestinal malrotation, and lethal congenital heart disease", "Cleft lip, cleft palate, characteristic facies, intestinal malrotation, and lethal congenital heart disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleft lip/palate-intestinal malrotation-cardiopathy syndrome", "shortest_name_length": 26}
{"curie": "UMLS:C5203818", "names": ["Borderline Ovarian Mixed Epithelial Tumor/Atypical Proliferative Ovarian Mixed Epithelial Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Ovarian Mixed Epithelial Tumor/Atypical Proliferative Ovarian Mixed Epithelial Tumor", "shortest_name_length": 95}
{"curie": "MONDO:0005558", "names": ["disease ovary", "ovary disease", "ovary disorder", "diseases ovary", "ovary diseases", "Ovary Disorders", "disease ovarian", "ovarian disease", "Ovarian Disease", "ovary disorders", "disorders ovary", "Ovarian disease", "disease ovaries", "Ovarian Disorder", "Disease, Ovarian", "Disease of ovary", "disease of ovary", "diseases ovaries", "ovarian disorder", "Ovarian Diseases", "DISORDER OVARIAN", "OVARIAN DISORDER", "Disorder ovarian", "Ovarian disorder", "disorder ovaries", "ovarian diseases", "Ovarian Disorders", "disorder of ovary", "ovarian disorders", "Diseases of Ovary", "Disorder of ovary", "disorders ovaries", "Ovaries--Diseases", "OVARIAN DISORDERS", "Diseases, Ovarian", "Ovarian disorder NOS", "Ovarian disorder, NOS", "Disease of ovary, NOS", "Abnormality of the ovary", "ovary disease or disorder", "Abnormality of the ovaries", "disease or disorder of ovary", "Disorder of ovary (disorder)", "disease (or disorder); ovary", "ovarian disorders (diagnosis)", "ovary (excluding endocrine function)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian disorder", "shortest_name_length": 13}
{"curie": "UMLS:C0422892", "names": ["Gestural Apraxia", "Gestural apraxia", "Apraxia, Gestural", "Gestural Apraxias", "Apraxias, Gestural", "Gestural apraxia (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Apraxia, Gestural", "shortest_name_length": 16}
{"curie": "MONDO:0009395", "names": ["VBCH", "VAN Buchem disease", "van Buchem Disease", "van Buchem disease", "VAN BUCHEM DISEASE", "Van Buchem disease", "Van Buchem Disease", "van Buchem's syndrome", "Endosteal hyperostosis", "endosteal hyperostosis", "Endosteal Hyperostosis", "Hyperphosphatasia tarda", "van Buchem Disease Type 1", "hyperphosphatasemia tarda", "Hyperphosphatasemia tarda", "van Buchem disease type 1", "HYPERPHOSPHATASEMIA TARDA", "Hyperphosphatasemia Tarda", "Hyperphosphatasaemia tarda", "Leontiasis ossea generalisata", "Sost Sclerosing Bone Dysplasia", "Hyperphosphatasemia tarda (disorder)", "Hyperostosis Corticalis Generalisata", "Hyperostosis corticalis generalisata", "HYPEROSTOSIS CORTICALIS GENERALISATA", "hyperostosis corticalis generalisata", "hyperphosphatasemia tarda (diagnosis)", "Sost-Related Sclerosing Bone Dysplasia", "SOST-related sclerosing bone dysplasia", "endosteal hyperostosis autosomal recessive", "endosteal hyperostosis, autosomal recessive", "ENDOSTEAL HYPEROSTOSIS, AUTOSOMAL RECESSIVE", "Endosteal Hyperostosis, Autosomal Recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperostosis corticalis generalisata", "shortest_name_length": 4}
{"curie": "MONDO:0023601", "names": ["NCCAH", "LOCAH", "Late onset congenital adrenal hyperplasia", "late-onset congenital adrenal hyperplasia", "Late-onset Congenital Adrenal Hyperplasia", "Attenuated congenital adrenal hyperplasia", "attenuated congenital adrenal hyperplasia", "Late-onset congenital adrenal hyperplasia", "non classic congenital adrenal hyperplasia", "Non classic congenital adrenal hyperplasia", "Non-Classic Congenital Adrenal Hyperplasia", "non-classic congenital adrenal hyperplasia", "LOCAH (late onset congenital adrenal hyperplasia)", "[OBSOLETE] Late-onset congenital adrenal hyperplasia", "Late onset congenital adrenal hyperplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-classic congenital adrenal hyperplasia", "shortest_name_length": 5}
{"curie": "MONDO:0019433", "names": ["Oligoarticular JIA", "Pauciarticular JIA", "Pauciarticular chronic arthritis", "Juvenile pauciarticular chronic arthritis", "oligoarticular juvenile idiopathic arthritis", "Oligoarticular Juvenile Idiopathic Arthritis", "Pauciarticular juvenile idiopathic arthritis", "Pauciarticular Juvenile Idiopathic Arthritis", "Oligoarticular juvenile idiopathic arthritis", "juvenile idiopathic arthritis, oligoarticular", "Juvenile idiopathic arthritis, oligoarthritis", "oligoarticular juvenile idiopathic arthritis (diagnosis)", "Juvenile idiopathic arthritis, oligoarthritis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oligoarticular juvenile idiopathic arthritis", "shortest_name_length": 18}
{"curie": "MONDO:0054813", "names": ["EDSCLL2", "clEDS type 2", "AEBP1-related EDS", "Classical-like EDS type 2", "AEBP1-related Ehlers-Danlos syndrome", "Ehlers-Danlos syndrome classic-like 2", "EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 2", "Ehlers-Danlos syndrome, classic-like, 2", "AEBP1-related EDS (Ehlers-Danlos syndrome)", "Classical-like Ehlers-Danlos syndrome type 2", "Classical-like Ehlers-Danlos syndrome type 2 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ehlers-Danlos syndrome, classic-like, 2", "shortest_name_length": 7}
{"curie": "UMLS:C0275550", "names": ["bacterial peritonitis", "Bacterial peritonitis NOS", "Acute bacterial peritonitis", "acute bacterial peritonitis", "Acute bacterial peritonitis (disorder)", "acute bacterial peritonitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute bacterial peritonitis", "shortest_name_length": 21}
{"curie": "UMLS:C1167753", "names": ["Parophthalmia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parophthalmia", "shortest_name_length": 13}
{"curie": "MONDO:0019411", "names": ["genochondromatosis type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genochondromatosis type 1", "shortest_name_length": 25}
{"curie": "MONDO:0020173", "names": ["skin of eyelid benign neoplasm", "benign tumor of palpebral epidermis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign tumor of palpebral epidermis", "shortest_name_length": 30}
{"curie": "MONDO:0016595", "names": ["LUNG, ANTHRAX", "Pulmonary anthrax", "Anthrax pneumonia", "Pneumonia anthrax", "ANTHRAX PNEUMONIA", "anthrax pneumonia", "pulmonary anthrax", "Anthrax, pulmonary", "pulmonary; anthrax", "anthrax inhalation", "WOOLSORTER DISEASE", "inhalation anthrax", "anthrax; pulmonary", "Inhalation anthrax", "respiratory anthrax", "inhalation; anthrax", "Respiratory anthrax", "anthrax; inhalation", "Woolsorter's disease", "woolsorters' disease", "inhalational anthrax", "anthrax; respiratory", "Woolsorters' disease", "Inhalational anthrax", "respiratory; anthrax", "Pneumonia in anthrax", "Wool-sorters' disease", "wool-sorters' disease", "woolsorter's; disease", "anthrax with pneumonia", "Pneumonia with anthrax", "Inhalation anthrax disease", "inhalation anthrax disease", "Respiratory anthrax disease", "respiratory anthrax disease", "Anthrax pneumonia (disorder)", "pneumonia; anthrax (etiology)", "pulmonary anthrax (diagnosis)", "anthrax; pneumonia (etiology)", "Inhalational anthrax (disorder)", "Inhalational anthrax (diagnosis)", "pneumonia; anthrax (manifestation)", "anthrax; pneumonia (manifestation)", "anthrax with pneumonia (diagnosis)", "disease (or disorder); ragpicker's", "disease (or disorder); woolsorter's", "pneumonia; Bacillus anthracis (etiology)", "pneumonia; Bacillus anthracis (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inhalational anthrax", "shortest_name_length": 13}
{"curie": "MONDO:0016751", "names": ["Perineural MPNST", "Malignant perineurioma", "Malignant Perineurioma", "malignant perineurioma", "Perineurioma, malignant", "perineurioma, malignant", "malignant perineurioma (diagnosis)", "Perineurioma, malignant (morphologic abnormality)", "perineurial malignant peripheral nerve sheath tumor", "Perineurial Malignant Peripheral Nerve Sheath Tumor", "Malignant Peripheral Nerve Sheath Tumor with Perineurial Differentiation", "Malignant peripheral nerve sheath tumor with perineurial differentiation", "malignant peripheral nerve sheath tumor with perineurial differentiation", "Malignant peripheral nerve sheath tumour with perineurial differentiation", "Malignant peripheral nerve sheath neoplasm with perineurial differentiation", "MPNST (malignant peripheral nerve sheath tumor) with perineurial differentiation", "MPNST (malignant peripheral nerve sheath tumour) with perineurial differentiation", "Malignant peripheral nerve sheath neoplasm with perineurial differentiation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant perineurioma", "shortest_name_length": 16}
{"curie": "MONDO:0011581", "names": ["DCWHK", "KWWH type II", "Carvajal syndrome", "CARVAJAL SYNDROME", "Keratoderma with wooly hair type II", "keratoderma with woolly hair type II", "Keratoderma with woolly hair type II", "dilated cardiomyopathy with woolly hair and keratoderma", "cardiomyopathy dilated with woolly hair and keratoderma", "Cardiomyopathy dilated with woolly hair and keratoderma", "CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR AND KERATODERMA", "Cardiomyopathy, Dilated, With Woolly Hair And Keratoderma", "cardiomyopathy, dilated, with woolly hair and keratoderma", "wooly hair - palmoplantar keratoderma - dilated cardiomyopathy", "arrhythmogenic cardiomyopathy with woolly hair and keratoderma", "wooly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome", "Wooly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome", "Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome", "wooly hair-palmoplantar hyperkeratosis-dilated cardiomyopathy syndrome", "Wooly hair-palmoplantar hyperkeratosis-dilated cardiomyopathy syndrome", "woolly hair-palmoplantar hyperkeratosis-dilated cardiomyopathy syndrome", "Woolly hair-palmoplantar hyperkeratosis-dilated cardiomyopathy syndrome", "woolly hair - palmoplantar keratoderma - dilated cardiomyopathy syndrome", "Wooly hair and palmoplantar keratoderma with dilated cardiomyopathy syndrome", "PALMOPLANTAR KERATODERMA WITH LEFT VENTRICULAR CARDIOMYOPATHY AND WOOLLY HAIR", "palmoplantar keratoderma with left ventricular cardiomyopathy and woolly hair", "Woolly hair and palmoplantar keratoderma with dilated cardiomyopathy syndrome", "epidermolytic palmoplantar keratoderma woolly hair and dilated cardiomyopathy", "Palmoplantar keratoderma with left ventricular cardiomyopathy and woolly hair", "Epidermolytic palmoplantar keratoderma, woolly hair, and dilated cardiomyopathy", "Wooly hair and palmoplantar keratoderma with dilated cardiomyopathy syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arrhythmogenic cardiomyopathy with woolly hair and keratoderma", "shortest_name_length": 5}
{"curie": "MONDO:0002063", "names": ["breast papillomatosis", "Breast Papillomatosis", "papillomatosis of breast", "Papillomatosis of Breast", "papillomatosis of the breast", "Papillomatosis of the Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast papillomatosis", "shortest_name_length": 21}
{"curie": "MONDO:0020693", "names": ["glycogen storage disease due to liver phosphorylase kinase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease due to liver phosphorylase kinase deficiency", "shortest_name_length": 69}
{"curie": "MONDO:0005775", "names": ["G6PD", "GPD Deficiency", "G6PD DEFICIENCY", "Deficiency;G6PD", "Deficiency, GPD", "deficiency g6pd", "G6PD deficiency", "G6PD Deficiency", "g6pd deficiency", "g-6pd deficiency", "Deficiency, G6PD", "GPD Deficiencies", "deficiency g 6 pd", "G-6 PD deficiency", "Deficiencies, GPD", "G6PD Deficiencies", "Deficiencies, G6PD", "deficiency of G-6PD", "Deficiency of G-6PD", "anemia g6pd hemolytic", "ANEMIA HEMOLYTIC G6PD", "Anemia hemolytic G6PD", "G6PD deficiency anemia", "ANEMIA DEFICIENCY G6PD", "G6PD deficiency anaemia", "ANAEMIA HAEMOLYTIC G6PD", "Anaemia haemolytic G6PD", "G-6-PD deficiency anemia", "anemia g-6-pd deficiency", "G-6-PD DEFICIENCY ANEMIA", "G-6-PD deficiency anaemia", "deficiency; anemia, G-6-PD", "anemia; deficiency, G-6-PD", "G6PD deficiency (diagnosis)", "G-6-PD deficiency anemia, NOS", "anemia due to G6PD deficiency", "G-6-PD deficiency anaemia, NOS", "Anemia hemolytic G6PD deficiency", "ANEMIA HEMOLYTIC G6PD DEFICIENCY", "Hemolytic anemia G6PD deficiency", "Anaemia haemolytic G6PD deficiency", "ANEMIA, HEMOLYTIC, G6PD DEFICIENCY", "G6PD deficiency anemia (diagnosis)", "Haemolytic anaemia G6PD deficiency", "G-6-PD Variant Enzyme Deficiency Anemia", "Hemolytic Anemia Due to G6PD Deficiency", "G-6-PD variant enzyme deficiency Anemia", "Glucosephosphate dehydrogenase deficiency", "Glucosephosphate Dehydrogenase Deficiency", "glucosephosphate dehydrogenase deficiency", "Deficiency, Glucosephosphate Dehydrogenase", "Dehydrogenase Deficiency, Glucosephosphate", "Glucosephosphate Dehydrogenase Deficiencies", "glucose 6 phosphate dehydrogenase deficiency", "glucose-6-phosphate dehydrogenase deficiency", "Deficiencies, Glucosephosphate Dehydrogenase", "Dehydrogenase Deficiencies, Glucosephosphate", "Glucose 6 Phosphate Dehydrogenase Deficiency", "Glucose-6-phosphate Dehydrogenase Deficiency", "Glucose-6-phosphate dehydrogenase deficiency", "Glucose-6-Phosphate Dehydrogenase Deficiency", "Deficiency, Glucose-6-Phosphate Dehydrogenase", "Dehydrogenase Deficiency, Glucose-6-Phosphate", "Glucose-6-Phosphate Dehydrogenase Deficiencies", "Deficiencies, Glucose-6-Phosphate Dehydrogenase", "Deficiency of glucose-6-phosphate dehydrogenase", "Deficiency of Glucose 6 Phosphate Dehydrogenase", "Deficiency of Glucose-6-Phosphate Dehydrogenase", "Dehydrogenase Deficiencies, Glucose-6-Phosphate", "Glucose-6-phosphate dehydrogenase deficiency anemia", "Glucose-6-phosphate dehydrogenase (G6PD) deficiency", "G6PD - Glucose-6-phosphate dehydrogenase deficiency", "Glucose-6-phosphate dehydrogenase deficiency anaemia", "anemia; glucose-6-phosphate dehydrogenase deficiency", "deficiency; glucose-6-phosphate dehydrogenase anemia", "glucose-6-phosphate dehydrogenase deficiency; anemia", "Glucose-6-phosphate dehydrogenase deficiency anemia, NOS", "Hemolytic anemia glucose-6-phos dehydrogenase deficiency", "Glucose-6-phosphate dehydrogenase deficiency anaemia, NOS", "glucose-6-phosphate dehydrogenase; deficiency with anemia", "Haemolytic anaemia glucose-6-phos dehydrogenase deficiency", "inborn glucose-6-phosphate dehydrogenase activity disorder", "Glucose-6-phosphate dehydrogenase deficiency (G6PD) anemia", "inborn error of glucose-6-phosphate dehydrogenase activity", "Deficiency of glucose-6-phosphate dehydrogenase (disorder)", "HEMOLYTIC ANEMIA GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENC", "deficiency; anemia, glucose-6-phosphate dehydrogenase (G-6-PD)", "Glucose-6-phosphate dehydrogenase deficiency anemia (disorder)", "anemia; deficiency, glucose-6-phosphate dehydrogenase (G-6-PD)", "rare inborn error of glucose-6-phosphate dehydrogenase activity", "Anemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency", "Anaemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency", "anemia; deficiency, enzyme, glucose-6-phosphate dehydrogenase (G-6-PD)", "deficiency; anemia, enzyme, glucose-6-phosphate dehydrogenase (G-6-PD)", "hemolytic; anemia, nonspherocytic, congenital or hereditary, glucose-6-phosphate dehydrogenase deficiency", "anemia; hemolytic, nonspherocytic, congenital or hereditary, glucose-6-phosphate dehydrogenase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "G6PD deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0000413", "names": ["infancy electroclinical syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infancy electroclinical syndrome", "shortest_name_length": 32}
{"curie": "MONDO:0016062", "names": ["Median cleft lip/mandibule", "Midline cleft of lower lip", "median cleft lip/mandibule", "median cleft lower facial stage", "Median cleft lower facial stage", "Midline cleft of lower lip (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "median cleft lip/mandibule", "shortest_name_length": 26}
{"curie": "MONDO:0022723", "names": ["Chondrodysplasia", "chondrodysplasia", "chondrodysplasias", "Chondrodysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chondrodysplasia", "shortest_name_length": 16}
{"curie": "MONDO:0011273", "names": ["HJCD", "SHML", "PHID", "H syndrome", "H SYNDROME", "Rosai–Dorfman disease", "Faisalabad histiocytosis", "FAISALABAD HISTIOCYTOSIS", "SLC29A3 spectrum disorder", "Asrar Facharzt Haque syndrome", "familial Rosai-Dorfman disease", "Rosai-Dorfman disease, familial", "ROSAI-DORFMAN DISEASE, FAMILIAL", "Histiocytosis-lymphadenopathy plus syndrome", "histiocytosis-lymphadenopathy plus syndrome", "HISTIOCYTOSIS-LYMPHADENOPATHY PLUS SYNDROME", "SINUS HISTIOCYTOSIS AND MASSIVE LYMPHADENOPATHY", "sinus histiocytosis and massive lymphadenopathy", "Histiocytosis-lymphadenopathy plus syndrome (disorder)", "histiocytosis with joint contractures and sensorineural deafness", "histiocytosis with Joint contractures and sensorineural deafness", "HISTIOCYTOSIS WITH JOINT CONTRACTURES AND SENSORINEURAL DEAFNESS", "Histiocytosis with joint contractures and sensorineural deafness", "pigmented hypertrichosis with insulin-dependent diabetes mellitus", "PIGMENTED HYPERTRICHOSIS WITH INSULIN-DEPENDENT DIABETES MELLITUS", "Pigmented Hypertrichosis With Insulin-Dependent Diabetes Mellitus Syndrome", "histiocytosis and lymphadenopathy with or without cutaneous, cardiac, and/or endocrine features, joint contractures and/or deafness", "cutaneous hyperpigmentation with hypertrichosis, hepatosplenomegaly, heart anomalies, and hypogonadism with or without hearing loss", "histiocytosis and lymphadenopathy with or without cutaneous, Cardiac, and/or endocrine features, Joint contractures, and/or deafness", "HISTIOCYTOSIS AND LYMPHADENOPATHY WITH OR WITHOUT CUTANEOUS, CARDIAC, AND/OR ENDOCRINE FEATURES, JOINT CONTRACTURES, AND/OR DEAFNESS", "Hyperpigmentation, Cutaneous, with Hypertrichosis, Hepatosplenomegaly, Heart Anomalies, and Hypogonadism With or Without Hearing Loss", "HYPERPIGMENTATION, CUTANEOUS, WITH HYPERTRICHOSIS, HEPATOSPLENOMEGALY, HEART ANOMALIES, AND HYPOGONADISM WITH OR WITHOUT HEARING LOSS", "hyperpigmentation, cutaneous, with hypertrichosis, hepatosplenomegaly, heart anomalies, and hypogonadism with or without hearing loss"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "H syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0005232", "names": ["Large Cell Carcinoma", "Large cell carcinoma", "large cell carcinoma", "LARGE CELL CARCINOMA", "Cell Carcinoma, Large", "Large Cell Carcinomas", "Carcinoma, Large Cell", "carcinoma, large cell", "Carcinomas, Large Cell", "Cell Carcinomas, Large", "Large cell carcinoma NOS", "Large cell carcinoma, NOS", "large cell carcinoma (diagnosis)", "Large cell carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "large cell carcinoma", "shortest_name_length": 20}
{"curie": "UMLS:C0278079", "names": ["addiction psychological", "Psychological addiction", "psychological addiction", "Dependence psychological", "Psychological Dependence", "DEPENDENCE PSYCHOLOGICAL", "Addiction, psychological", "psychological dependence", "Psychological dependence", "Dependence, psychological", "psychological AOD dependence", "Psychological addiction (finding)", "psychological alcohol or other drug dependence", "psychological Alcohol or Other Drugs dependence"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Psychological Dependence", "shortest_name_length": 23}
{"curie": "MONDO:0014247", "names": ["FEPS3", "familial episodic pain syndrome 3", "Episodic Pain Syndrome, Familial, 3", "episodic pain syndrome, familial, 3", "EPISODIC PAIN SYNDROME, FAMILIAL, 3", "episodic pain syndrome, familial, type 3", "Familial episodic pain syndrome with predominantly lower limb involvement", "familial episodic pain syndrome with predominantly lower limb involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial episodic pain syndrome with predominantly lower limb involvement", "shortest_name_length": 5}
{"curie": "UMLS:C4552677", "names": ["Stage I Renal Pelvis and Ureter Cancer", "stage I renal pelvis and ureter cancer AJCC v8", "Stage I Renal Pelvis and Ureter Cancer AJCC v8", "stage I renal pelvis and ureter urothelial carcinoma AJCC v8", "Stage I Renal Pelvis and Ureter Urothelial Carcinoma AJCC v8", "stage I transitional cell cancer of the renal pelvis and ureter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Renal Pelvis and Ureter Cancer AJCC v8", "shortest_name_length": 38}
{"curie": "MONDO:0017250", "names": ["CPAM type 2", "CCAM type 2", "congenital cystic disease of the lung type 2", "congenital pulmonary airway malformation type 2", "congenital cystic adenomatous malformation of the lung type 2", "congenital cystic adenomatoid malformation of the lung type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital pulmonary airway malformation type 2", "shortest_name_length": 11}
{"curie": "MONDO:0017943", "names": ["GDS", "Gardner-Diamond", "Factitious purpura", "psychogenic purpura", "Psychogenic purpura", "Purpura, psychogenic", "gardner-diamond syndrome", "GARDNER-DIAMOND SYNDROME", "gardner diamond syndrome", "Gardner-Diamond syndrome", "Gardener-Diamond syndrome", "painful bruising syndrome", "gardener diamond syndrome", "PAINFUL BRUISING SYNDROME", "Painful bruising syndrome", "autoerythrocyte sensitivity", "Autoerythrocyte sensitivity", "Autoerythrocyte sensitization", "autoerythrocyte sensitization", "Auto-erythrocyte sensitization", "Auto-erythrocyte sensitisation", "auto erythrocyte sensitization", "psychogenic purpura (diagnosis)", "Gardner-Diamond syndrome (disorder)", "Autoerythrocyte sensitivity disorder", "Autoerythrocyte sensitization purpura", "Autoerythrocyte sensitisation purpura", "Autoerythrocyte sensitisation syndrome", "Autoerythrocyte sensitization syndrome", "autoerythrocyte sensitization syndrome", "AUTOERYTHROCYTE SENSITIZATION SYNDROME", "syndrome; autoerythrocyte sensitization", "Auto-erythrocyte sensitisation syndrome", "Auto-erythrocyte sensitization syndrome", "autoerythrocyte sensitization; syndrome", "Autoerythrocyte sensitivity disorder, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoerythrocyte sensitization syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0019007", "names": ["vaginal atresia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vaginal atresia", "shortest_name_length": 15}
{"curie": "MONDO:0018082", "names": ["Aortoventricular Tunnel", "Aorto-Ventricular Tunnel", "Aorto Ventricular Tunnel", "Aorto-ventricular tunnel", "aorto-ventricular tunnel", "Aortoventricular Tunnels", "Aorticoventricular Tunnel", "Aortic-Ventricular Tunnel", "Aortic Ventricular Tunnel", "Aorto-Ventricular Tunnels", "Aortic-Ventricular Tunnels", "Aorticoventricular Tunnels", "Aortico-Ventricular Tunnel", "Tunnel, Aorticoventricular", "Aortico Ventricular Tunnel", "Aortico-Ventricular Tunnels", "aorto-ventricular tunnel (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aorto-ventricular tunnel", "shortest_name_length": 23}
{"curie": "UMLS:C1332181", "names": ["adult AMOL", "AMOL, adult", "M5 adult AMOL", "monocytic leukemia, adult acute", "acute monocytic leukemia, adult", "leukemia, adult acute monocytic", "M5 adult acute monocytic leukemia", "Acute Monoblastic and Monocytic Leukemia", "M5 OR Acute Monoblastic/Monocytic Leukemia", "Adult Acute Monoblastic and Monocytic Leukemia", "M5 Adult Acute Monoblastic and Monocytic Leukemia", "Adult Acute Monoblastic and Monocytic Leukemia (M5)", "Adult Acute Monoblastic and Monocytic Leukemia (FAB M5)", "Adult Acute Monoblastic Leukemia and Acute Monocytic Leukemia", "adult acute monoblastic leukemia and acute monocytic leukemia (M5)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Acute Monoblastic and Monocytic Leukemia", "shortest_name_length": 10}
{"curie": "MONDO:0012534", "names": ["COXPD4", "Combined Oxidative Phosphorylation Deficiency 4", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 4", "combined oxidative phosphorylation deficiency 4", "Combined oxidative phosphorylation defect type 4", "combined oxidative phosphorylation defect type 4", "TUFM combined oxidative phosphorylation deficiency", "combined oxidative phosphorylation deficiency type 4", "COXPD4 - combined oxidative phosphorylation defect type 4", "Combined oxidative phosphorylation defect type 4 (disorder)", "combined oxidative phosphorylation defect type 4 (diagnosis)", "combined oxidative phosphorylation deficiency caused by mutation in TUFM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation defect type 4", "shortest_name_length": 6}
{"curie": "UMLS:C5555151", "names": ["Bone Langerhans Cell Histiocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone Langerhans Cell Histiocytosis", "shortest_name_length": 34}
{"curie": "MONDO:0014692", "names": ["RP74", "RETINITIS PIGMENTOSA 74", "retinitis pigmentosa 74", "BBS2 retinitis pigmentosa", "retinitis pigmentosa type 74", "retinitis pigmentosa caused by mutation in BBS2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 74", "shortest_name_length": 4}
{"curie": "MONDO:0001162", "names": ["ICD", "impulse-control disorder", "Impulse control disorder", "Impulse-control disorder", "control disorder impulse", "impulse control disorder", "Impulse-Control Disorder", "IMPULSE CONTROL DISORDER", "Impulse Control Disorder", "Impulse-Control Disorders", "impulse-control disorders", "Impulse Control Disorders", "IMPULSE CONTROL DISORDERS", "Impulse control disorders", "impulse control disorders", "Habit and impulse disorder", "Disorders, Impulse Control", "Habit and impulse disorders", "Impulse control disorder NOS", "Impulse-control disorder NOS", "Impulse control disorder, NOS", "Impulse control disorder (disorder)", "impulse control disorder (diagnosis)", "Impulse control disorder, unspecified", "Habit and impulse disorder, unspecified", "disruptive impulse control and conduct disorder", "Disruptive, impulse-control and conduct disorders", "disruptive, impulse-control, and conduct disorder", "Disruptive, Impulse Control, and Conduct Disorders", "disruptive, impulse-control, and conduct disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "impulse control disorder", "shortest_name_length": 3}
{"curie": "MONDO:0014504", "names": ["PRLTS5", "Perrault syndrome 5", "PERRAULT SYNDROME 5", "TWNK Perrault syndrome", "Perrault syndrome type 5", "Perrault syndrome caused by mutation in TWNK"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perrault syndrome 5", "shortest_name_length": 6}
{"curie": "MONDO:0003076", "names": ["unilateral retinoblastoma", "Unilateral Retinoblastoma", "Retinoblastoma unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "unilateral retinoblastoma", "shortest_name_length": 25}
{"curie": "MONDO:0018158", "names": ["mtDNA depletion syndrome", "mitochondrial DNA depletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial DNA depletion syndrome", "shortest_name_length": 24}
{"curie": "MONDO:0004185", "names": ["ovary serous cystadenofibroma", "Ovarian serous cystadenofibroma", "Ovarian Serous Cystadenofibroma", "ovarian serous cystadenofibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian serous cystadenofibroma", "shortest_name_length": 29}
{"curie": "MONDO:0008311", "names": ["Baraitser syndrome", "progeria-like syndrome", "Mulvihill-Smith Syndrome", "Mulvihill-Smith syndrome", "MULVIHILL-SMITH SYNDROME", "Progeria short stature pigmented nevi", "Progeroid Short Stature with Pigmented Nevi", "progeroid short stature with pigmented nevi", "Progeroid short stature with pigmented nevi", "PROGEROID SHORT STATURE WITH PIGMENTED NEVI", "Progeroid short stature with pigmented naevi", "Progeria-short stature-pigmented nevi syndrome", "progeria-short stature-pigmented nevi syndrome", "progeroid short stature-pigmented nevi syndrome", "Progeroid short stature with pigmented nevi (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progeria-short stature-pigmented nevi syndrome", "shortest_name_length": 18}
{"curie": "UMLS:C2113596", "names": ["Idiopathic Precocious Puberty", "idiopathic precocious puberty", "idiopathic precocious puberty (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic precocious puberty", "shortest_name_length": 29}
{"curie": "MONDO:0043455", "names": ["HHM", "hhm", "MAHC", "mahc", "Malignant hypercalcemia", "malignant hypercalcemia", "Malignant hypercalcaemia", "HYPERCALCEMIA OF MALIGNANCY", "Hypercalcemia of malignancy", "hypercalcemia of malignancy", "Hypercalcemia of Malignancy", "Hypercalcaemia of malignancy", "hypercalcaemia of malignancy", "Paraneoplastic hypercalcemia", "Paraneoplastic hypercalcaemia", "Humoral hypercalcemia of malignancy", "humoral hypercalcemia of malignancy", "malignancy associated hypercalcemia", "Malignancy associated hypercalcemia", "Humoral Hypercalcemia Of Malignancy", "Humoral hypercalcaemia of malignancy", "Malignancy associated hypercalcaemia", "Humoural hypercalcaemia of malignancy", "Humoral hypercalcemia of malignancy (disorder)", "humoral hypercalcemia of malignancy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "humoral hypercalcemia of malignancy", "shortest_name_length": 3}
{"curie": "UMLS:C5418951", "names": ["Supratentorial Gliosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Supratentorial Gliosarcoma", "shortest_name_length": 26}
{"curie": "UMLS:C0334033", "names": ["TCM", "Metaplasia, transitional", "Transitional cell metaplasia", "Transitional Cell Metaplasia", "Transitional cell metaplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transitional cell metaplasia", "shortest_name_length": 3}
{"curie": "MONDO:0008424", "names": ["Bridged sella turcica", "Sella Turcica, Bridged", "SELLA TURCICA, BRIDGED", "sella turcica, bridged"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sella turcica, bridged", "shortest_name_length": 21}
{"curie": "MONDO:0005103", "names": ["ALT", "WDLS", "atypical lipoma", "Atypical lipoma", "Lipoma-Like ALT/WDLPS", "Lipoma-Like Liposarcoma", "Lipoma-like liposarcoma", "Atypical lipomatous tumor", "Atypical Lipomatous Tumor", "atypical lipomatous tumor", "Lipomatous Tumor, Atypical", "Atypical Lipomatous Tumors", "Liposarcoma, differentiated", "Liposarcoma - differentiated", "Well-Differentiated Liposarcoma", "well differentiated liposarcoma", "Well Differentiated Liposarcoma", "Well-differentiated liposarcoma", "well-differentiated liposarcoma", "Liposarcoma, well differentiated", "Liposarcoma, Well Differentiated", "Well Differentiated Liposarcomas", "Liposarcoma - well differentiated", "well differentiated liposarcoma (diagnosis)", "well differentiated liposarcoma of deep soft tissue", "Liposarcoma, well differentiated (morphologic abnormality)", "Lipoma-Like Atypical Lipomatous Tumor/Well Differentiated Liposarcoma", "Lipoma-Like Atypical Lipomatous Tumor/Well-Differentiated Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "well-differentiated liposarcoma", "shortest_name_length": 3}
{"curie": "UMLS:C0043065", "names": ["Water Electrolyte Imbalance", "Water-Electrolyte Imbalance", "water electrolyte imbalance", "water-electrolyte imbalance", "Water-Electrolyte Imbalances", "Water-electrolyte imbalances", "Imbalance, Water-Electrolyte", "Imbalances, Water-Electrolyte"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Water-Electrolyte Imbalance", "shortest_name_length": 27}
{"curie": "MONDO:0044743", "names": ["major salivary gland cancer", "cancer of major salivary gland", "malignant major salivary gland tumor", "Malignant Major Salivary Gland Tumor", "malignant major salivary gland neoplasm", "Malignant Major Salivary Gland Neoplasm", "malignant salivary gland neoplasm major", "malignant tumor of major salivary gland", "Malignant Tumor of Major Salivary Gland", "Malignant tumor of major salivary gland", "Malignant tumour of major salivary gland", "Malignant neoplasm of major salivary gland", "Malignant Neoplasm of Major Salivary Gland", "malignant neoplasm of major salivary gland", "Malignant Tumor of the Major Salivary Gland", "Malignant neoplasm of major salivary glands", "malignant tumor of the major salivary gland", "malignant neoplasm of major salivary glands", "malignant neoplasm of the major salivary gland", "Malignant neoplasm of major salivary gland NOS", "Malignant Neoplasm of the Major Salivary Gland", "Malignant neoplasm of major salivary gland, NOS", "Malignant neoplasm of salivary gland (major) NOS", "Malignant tumor of major salivary gland (disorder)", "malignant neoplasm of major salivary gland (diagnosis)", "Malignant neoplasm of major salivary gland, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "major salivary gland cancer", "shortest_name_length": 27}
{"curie": "MONDO:0018156", "names": ["Del(3)(q26q27)", "monosomy 3q26q27", "monosomy 3q26-q27", "3q26-q27microdeletion syndrome", "3q26q27 microdeletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "3q26q27 microdeletion syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C4038952", "names": ["Metastatic thymic carcinoma", "Metastatic Thymic Carcinoma", "Metastatic thymic carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic thymic carcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0100460", "names": ["SMOKING HABIT, SUSCEPTIBILITY TO", "smoking habit, susceptibility to", "susceptibility to tobacco addiction", "nicotine addiction, protection from", "tobacco addiction, susceptibility to", "TOBACCO ADDICTION, SUSCEPTIBILITY TO", "nicotine addiction, susceptibility to", "NICOTINE ADDICTION, SUSCEPTIBILITY TO", "nicotine dependence, susceptibility to", "NICOTINE DEPENDENCE, SUSCEPTIBILITY TO", "NICOTINE DEPENDENCE, PROTECTION AGAINST", "nicotine dependence, protection against", "cigarette habituation, susceptibility to", "CIGARETTE HABITUATION, SUSCEPTIBILITY TO", "TOBACCO ADDICTION, SUSCEPTIBILITY TO (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tobacco addiction, susceptibility to", "shortest_name_length": 32}
{"curie": "UMLS:C2350876", "names": ["Exudative Bronchiolitis", "Bronchiolitis exudativa", "Bronchiolitis, Exudative", "Exudative Bronchiolitides", "Bronchiolitides, Exudative", "Bronchiolitis exudativa (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bronchiolitis, Exudative", "shortest_name_length": 23}
{"curie": "MONDO:0033664", "names": ["KILQS", "KILQUIST SYNDROME", "Kilquist syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kilquist syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0013177", "names": ["ITGA7 congenital muscular dystrophy", "congenital muscular dystrophy with ITGA7 deficiency", "Congenital muscular dystrophy with ITGA7 deficiency", "congenital myopathy due to integrin alpha-7 deficiency", "muscular dystrophy, congenital, due to ITGA7 deficiency", "myopathy, congenital, due to integrin Alpha-7 deficiency", "Myopathy, Congenital, Due To Integrin Alpha-7 Deficiency", "MYOPATHY, CONGENITAL, DUE TO INTEGRIN ALPHA-7 DEFICIENCY", "congenital muscular dystrophy caused by mutation in ITGA7", "Congenital muscular dystrophy with integrin alpha-7 deficiency", "congenital muscular dystrophy with integrin alpha-7 deficiency", "congenital muscular dystrophy due to integrin alpha-7 deficiency", "muscular dystrophy, congenital, due to integrin ALPHA-7 deficiency", "MUSCULAR DYSTROPHY, CONGENITAL, DUE TO INTEGRIN ALPHA-7 DEFICIENCY", "Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency", "Congenital muscular dystrophy with ITGA7 (integrin alpha-7) deficiency", "Congenital muscular dystrophy with integrin alpha-7 deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital muscular dystrophy due to integrin alpha-7 deficiency", "shortest_name_length": 35}
{"curie": "UMLS:C4521713", "names": ["IVA", "Stage IVA Esophageal Adenocarcinoma", "Pathologic Stage IVA Esophageal Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IVA Esophageal Adenocarcinoma AJCC v8", "shortest_name_length": 3}
{"curie": "MONDO:0043125", "names": ["McPherson Robertson Cammarano syndrome", "mcpherson robertson cammarano syndrome", "dominantly inherited ptosis, strabismus and ectopic pupils", "Dominantly inherited ptosis, strabismus and ectopic pupils"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mcpherson robertson cammarano syndrome", "shortest_name_length": 38}
{"curie": "DOID:8642", "names": ["Hodgkin paragranuloma", "Hodgkin's paragranuloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's paragranuloma", "shortest_name_length": 21}
{"curie": "UMLS:C0497248", "names": ["Hypertension;uncomplicated", "Uncomplicated hypertension", "uncomplicated hypertension", "Hypertension uncomplicated", "Uncomplicated Hypertension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uncomplicated hypertension", "shortest_name_length": 26}
{"curie": "UMLS:C1332214", "names": ["Primary Cutaneous Anaplastic Large Cell Lymphoma", "Adult Primary Cutaneous Anaplastic Large Cell Lymphoma", "Adult Primary Cutaneous K-1+ Anaplastic Large Cell Lymphoma", "Adult Primary Cutaneous CD30+ Anaplastic Large Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Primary Cutaneous Anaplastic Large Cell Lymphoma", "shortest_name_length": 48}
{"curie": "MONDO:0015279", "names": ["CMC", "CANDF", "familial CMC", "familial candidiasis", "Mucocutaneous candidiasis", "CHRONIC MUCOCUTANEOUS CANDIDOSIS", "Chronic Mucocutaneous Candidiasis", "CHRONIC MUCOCUTANEOUS CANDIDIASIS", "candidiasis chronic mucocutaneous", "chronic mucocutaneous candidiasis", "Chronic mucocutaneous candidiasis", "Chronic Mucocutaneous Candidiases", "Candidiasis, Chronic Mucocutaneous", "Mucocutaneous Candidiases, Chronic", "Mucocutaneous Candidiasis, Chronic", "Candidiases, Chronic Mucocutaneous", "CMC - Chronic mucocutaneous candidiasis", "familial chronic mucocutaneous candidiasis", "chronic mucocutaneous candidiasis (disease)", "Chronic mucocutaneous candidiasis (disorder)", "Chronic candidiasis of mucosa, skin and nails", "chronic mucocutaneous candidiasis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic mucocutaneous candidiasis", "shortest_name_length": 3}
{"curie": "MONDO:0003458", "names": ["corpus uteri adenofibroma", "Uterine Body Adenofibroma", "Corpus Uteri Adenofibroma", "uterine body adenofibroma", "body of uterus adenofibroma", "Uterine Corpus Adenofibroma", "uterine corpus adenofibroma", "Adenofibroma of Corpus Uteri", "adenofibroma of uterine body", "adenofibroma of corpus uteri", "Adenofibroma of Uterine Body", "adenofibroma of Corpus Uteri", "adenofibroma of uterine corpus", "Adenofibroma of Uterine Corpus", "adenofibroma of body of uterus", "Adenofibroma of Body of Uterus", "Adenofibroma of the Corpus Uteri", "Adenofibroma of the Uterine Body", "adenofibroma of the uterine body", "adenofibroma of the corpus uteri", "Adenofibroma of the Body of Uterus", "adenofibroma of the uterine corpus", "adenofibroma of the body of uterus", "Adenofibroma of the Uterine Corpus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine corpus adenofibroma", "shortest_name_length": 25}
{"curie": "MONDO:0012533", "names": ["AUTS7", "autism susceptibility 7", "autism, susceptibility to, 7", "AUTISM, SUSCEPTIBILITY TO, 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autism, susceptibility to, 7", "shortest_name_length": 5}
{"curie": "UMLS:C0948395", "names": ["Gastrointestinal hypermotility"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal hypermotility", "shortest_name_length": 30}
{"curie": "UMLS:C0268849", "names": ["Overactive detrusor", "Overactive Detrusor", "Detrusor, Overactive", "Detrusor overactivity", "Overactive Detrusor Function", "Detrusor Function, Overactive", "Detrusor overactivity (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Overactive Detrusor", "shortest_name_length": 19}
{"curie": "UMLS:C1439275", "names": ["Disseminated carcinoma", "Disseminated Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disseminated carcinoma", "shortest_name_length": 22}
{"curie": "UMLS:C0278569", "names": ["Mycosis fungoides stage II", "Mycosis Fungoides Stage II", "Stage II Mycosis Fungoides", "Stage II Mycosis Fungoides AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mycosis fungoides stage II", "shortest_name_length": 26}
{"curie": "MONDO:0009663", "names": ["Mucus Inspissation of Respiratory Tract", "mucus inspissation of respiratory tract", "MUCUS INSPISSATION OF RESPIRATORY TRACT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucus inspissation of respiratory tract", "shortest_name_length": 39}
{"curie": "MONDO:0014214", "names": ["SRPS6", "SRTD8", "short rib-polydactyly syndrome type VI", "short rib-polydactyly syndrome, type 6", "SHORT RIB-POLYDACTYLY SYNDROME, TYPE VI", "short-rib thoracic dysplasia 8 with or without polydactyly", "SHORT-RIB THORACIC DYSPLASIA 8 WITH OR WITHOUT POLYDACTYLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short-rib thoracic dysplasia 8 with or without polydactyly", "shortest_name_length": 5}
{"curie": "UMLS:C0040428", "names": ["tooth abrasion", "Tooth abrasion", "Tooth Abrasion", "abrasion dental", "abrasions tooth", "abrasion; teeth", "dental abrasion", "Dental Abrasion", "teeth; abrasion", "Teeth--Abrasion", "Abrasion, Tooth", "Dental abrasion", "Abrasion, Dental", "Abrasion of tooth", "abrasion of teeth", "Abrasion of teeth", "Abrasion of teeth, NOS", "Friction injury of tooth", "abrasion of teeth (diagnosis)", "Friction injury of tooth (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tooth Abrasion", "shortest_name_length": 14}
{"curie": "UMLS:C0272687", "names": ["closed fracture of shaft of metacarpal bone", "Closed fracture of shaft of metacarpal bone", "Closed Fracture of Shaft of Metacarpal Bone", "Closed fracture of shaft of metacarpal bones", "Closed fracture of shaft of metacarpal bone(s)", "Closed fracture of shaft of metacarpal bone (disorder)", "closed fracture of shaft of metacarpal bone (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Closed fracture of shaft of metacarpal bone", "shortest_name_length": 43}
{"curie": "MONDO:0024582", "names": ["male reproductive organ tumor", "Male Reproductive System Tumor", "Male reproductive system tumor", "male reproductive organ neoplasm", "tumor of male reproductive organ", "male reproductive system neoplasm", "Tumor of Male Reproductive System", "tumor of Male reproductive system", "Male Reproductive System Neoplasm", "Male reproductive system neoplasm", "neoplasm of male reproductive organ", "neoplasm of Male reproductive system", "Neoplasm of Male Reproductive System", "tumor of the Male reproductive system", "Tumor of the Male Reproductive System", "Neoplasm of the Male Reproductive System", "neoplasm of the Male reproductive system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "male reproductive system neoplasm", "shortest_name_length": 29}
{"curie": "MONDO:0008294", "names": ["AIP", "PORC", "UPS deficiency", "UPS DEFICIENCY", "UPS Deficiency", "Acute porphyria", "PBGD deficiency", "Acute Porphyria", "porphyria acute", "HMBS deficiency", "Porphyria acute", "Deficiency, UPS", "acute porphyria", "PBGD Deficiency", "PBGD DEFICIENCY", "UPS Deficiencies", "Acute Porphyrias", "Porphyria, Acute", "pyrroloporphyria", "Deficiency, PBGD", "acute porphyrias", "Pyrroloporphyria", "Deficiencies, UPS", "Pyrrole porphyria", "Porphyrias, Acute", "PBGD Deficiencies", "Swedish porphyria", "Deficiencies, PBGD", "Swedish Type Porphyria", "Chester-type porphyria", "PORPHYRIA, SWEDISH TYPE", "PORPHYRIA, CHESTER TYPE", "porphyria, Chester type", "Porphyria, Swedish Type", "Swedish Type Porphyrias", "Type Porphyria, Swedish", "Porphyria, Chester type", "porphyria, Swedish type", "Type Porphyrias, Swedish", "Porphyrias, Swedish Type", "Swedish genetic porphyria", "Intermittent acute porphyria", "Acute intermittent porphyria", "PORPHYRIA ACUTE INTERMITTENT", "acute intermittent porphyria", "Acute Intermittent Porphyria", "porphyria intermittent acute", "PORPHYRIA, ACUTE INTERMITTENT", "Intermittent Porphyria, Acute", "Porphyria, Acute Intermittent", "Porphyria, acute intermittent", "Acute Intermittent Porphyrias", "porphyria, acute intermittent", "porphyria; acute intermittent", "acute intermittent porphyrias", "acute; intermittent porphyria", "Intermittent Porphyrias, Acute", "Porphyrias, Acute Intermittent", "Chester-type porphyria (disorder)", "acute intermittent porphyria (AIP)", "AIP (acute intermittent porphyria)", "AIP - acute intermittent porphyria", "AIP - Acute intermittent porphyria", "uroporphyrinogen synthase deficiency", "PORPHOBILINOGEN DEAMINASE DEFICIENCY", "porphobilinogen deaminase deficiency", "Porphobilinogen deaminase deficiency", "Uroporphyrinogen Synthase Deficiency", "Porphobilinogen Deaminase Deficiency", "UROPORPHYRINOGEN SYNTHASE DEFICIENCY", "Deficiency, Porphobilinogen Deaminase", "Deficiency, Uroporphyrinogen Synthase", "Deaminase Deficiency, Porphobilinogen", "Synthase Deficiency, Uroporphyrinogen", "Intermittent acute porphyria syndrome", "Uroporphyrinogen 1 synthase deficiency", "Porphobilinogen Deaminase Deficiencies", "Uroporphyrinogen Synthase Deficiencies", "Deaminase Deficiencies, Porphobilinogen", "Acute intermittent porphyria (disorder)", "Deficiencies, Uroporphyrinogen Synthase", "Synthase Deficiencies, Uroporphyrinogen", "hydroxymethylbilane synthase deficiency", "Hydroxymethylbilane Synthase Deficiency", "Deficiencies, Porphobilinogen Deaminase", "Synthase Deficiency, Hydroxymethylbilane", "Deficiency, Hydroxymethylbilane Synthase", "acute intermittent porphyria (diagnosis)", "Hydroxymethylbilane Synthase Deficiencies", "Synthase Deficiencies, Hydroxymethylbilane", "Deficiencies, Hydroxymethylbilane Synthase", "PBGD - Porphobilinogen deaminase deficiency", "Porphobilinogen deaminase deficiency (disorder)", "porphyria, acute intermittent, Nonerythroid variant", "PORPHYRIA, ACUTE INTERMITTENT, NONERYTHROID VARIANT", "Porphyria, Acute Intermittent, Nonerythroid Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute intermittent porphyria", "shortest_name_length": 3}
{"curie": "MONDO:0022394", "names": ["cin", "CIN", "Cervical Dysplasia", "dysplasia of cervix", "dysplasia of cervix (uteri)", "dysplasia of uterine cervix", "Cervical intraepith. neoplasia", "NEOPL CERVICAL INTRAEPITHELIAL", "Cervix Intraepithelial Neoplasia", "Cervical Intraepithelial Neoplasm", "cervix; intraepithelial neoplasia", "Cervical Intraepithelial Neoplasms", "Neoplasm, Cervical Intraepithelial", "Cervical Intraepithelial Neoplasia", "cervical intra-epithelial neoplasm", "precancerous changes of the cervix", "cervical intraepithelial neoplasia", "neoplasia; intraepithelial, cervix", "Cervical intraepithelial neoplasia", "Intraepithelial Neoplasm, Cervical", "Intraepithelial Neoplasms, Cervical", "Neoplasia, Cervical Intraepithelial", "Intraepithelial Neoplasia of Cervix", "Intraepithelial Neoplasia, Cervical", "Neoplasms, Cervical Intraepithelial", "Cervical intraepithelial neoplasia NOS", "Cervix Uteri Intraepithelial Neoplasia", "dysplasia of uterine cervix (diagnosis)", "Intraepithelial Neoplasia of the Cervix", "Cervical intraepithelial neoplasia (CIN)", "Uterine Cervix Intraepithelial Neoplasia", "CIN - Cervical intraepithelial neoplasia", "cervical intraepithelial neoplasia (CIN)", "Intraepithelial Neoplasia of Cervix Uteri", "Intraepithelial Neoplasia of Uterine Cervix", "Intraepithelial Neoplasia of the Cervix Uteri", "Cervical intraepithelial neoplasia (disorder)", "cervical intraepithelial neoplasia (diagnosis)", "Intraepithelial Neoplasia of the Uterine Cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical intraepithelial neoplasia", "shortest_name_length": 3}
{"curie": "MONDO:0004181", "names": ["breast adenomyoepithelial adenosis", "Breast Adenomyoepithelial Adenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast adenomyoepithelial adenosis", "shortest_name_length": 34}
{"curie": "MONDO:0017439", "names": ["Tetraamelia", "Tetra-Amelia", "total amelia", "Tetra-amelia", "Total amelia", "tetra-amelia", "Tetra-amelia syndrome", "Tetra-Amelia Syndrome", "tetra-amelia syndrome", "Autosomal recessive tetra-amelia", "Tetra-amelia autosomal recessive", "Tetra-amelia syndrome (disorder)", "Tetraamelia, autosomal recessive", "Tetraamelia, Autosomal Recessive", "Tetra-Amelia, Autosomal Recessive", "tetra-amelia, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tetra-amelia", "shortest_name_length": 11}
{"curie": "MONDO:0007222", "names": ["BDD", "STUB THUMB", "Stub Thumb", "stub thumb", "Stub thumb", "Stub thumbs", "Type D brachydactyly", "Brachydactyly type D", "brachydactyly type D", "Brachydactyly, Type D", "BRACHYDACTYLY, TYPE D", "brachydactyly, type D", "Brachydactyly type D (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly type D", "shortest_name_length": 3}
{"curie": "UMLS:C0919593", "names": ["Injection site coldness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site coldness", "shortest_name_length": 23}
{"curie": "MONDO:0032890", "names": ["NMOAS", "NEUROMUSCULAR OCULOAUDITORY SYNDROME", "NEUROMUSCULAR DISEASE AND OCULAR OR AUDITORY ANOMALIES WITH OR WITHOUT SEIZURES", "neuromuscular disease and ocular or auditory anomalies with or without seizures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuromuscular disease and ocular or auditory anomalies with or without seizures", "shortest_name_length": 5}
{"curie": "UMLS:C5419768", "names": ["Gastroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastroblastoma", "shortest_name_length": 14}
{"curie": "MONDO:0000607", "names": ["CTCL", "PCTCL", "Cutaneous lymphoma", "cutaneous T-cell lymphoma", "t cell cutaneous lymphoma", "Cutaneous T-cell lymphoma", "Cutaneous T-Cell Lymphoma", "cutaneous t-cell lymphoma", "CUTANEOUS T CELL LYMPHOMA", "Cutaneous T Cell Lymphoma", "cutaneous t cell lymphoma", "cutaneous T cell lymphoma", "CUTANEOUS T-CELL LYMPHOMA", "T Cell Lymphoma, Cutaneous", "T-cell lymphoma, cutaneous", "Lymphoma, Cutaneous T-Cell", "T cell lymphoma, cutaneous", "T-Cell Lymphoma, Cutaneous", "lymphoma, cutaneous T-cell", "Cutaneous T-Cell Lymphomas", "Lymphoma, T-Cell, Cutaneous", "Lymphoma, T Cell, Cutaneous", "Lymphomas, Cutaneous T-Cell", "T-Cell Lymphomas, Cutaneous", "cells cutaneous lymphomas t", "CTCL - Cutaneous T-cell lymphoma", "Primary cutaneous T-cell lymphoma", "skin T-cell non-Hodgkin's lymphoma", "Skin T-Cell Non-Hodgkin's Lymphoma", "Cutaneous T-Cell Non-Hodgkin Lymphoma", "T-cell non-Hodgkin's lymphoma of skin", "Cutaneous T-cell lymphoma (diagnosis)", "cutaneous T-cell non-Hodgkin lymphoma", "T-Cell Non-Hodgkin's Lymphoma of Skin", "Cutaneous T-Cell Non-Hodgkin's Lymphoma", "cutaneous T-cell non-Hodgkin's lymphoma", "T-cell non-Hodgkin's lymphoma of the skin", "T-Cell Non-Hodgkin's Lymphoma of the Skin", "Primary cutaneous T-cell lymphoma (disorder)", "primary cutaneous T-cell non-Hodgkin lymphoma", "Primary Cutaneous T-Cell Non-Hodgkin Lymphoma", "Primary cutaneous T-cell lymphoma (diagnosis)", "primary cutaneous T-cell non-Hodgkin's lymphoma", "Primary Cutaneous T-Cell Non-Hodgkin's Lymphoma", "Cutaneous T-cell lymphoma (morphologic abnormality)", "Primary cutaneous T-cell lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary cutaneous T-cell non-Hodgkin lymphoma", "shortest_name_length": 4}
{"curie": "MONDO:0005827", "names": ["Lipoatrophic Diabete", "lipoatrophic diabete", "Lipoatrophic Diabetes", "Diabete, Lipoatrophic", "Lipoatrophic diabetes", "lipoatrophic diabetes", "diabete, lipoatrophic", "diabetes, lipoatrophic", "DIABETES, LIPOATROPHIC", "Diabetes, Lipoatrophic", "Lipodystrophic diabetes", "Lipoatrophic diabetes, NOS", "Lipodystrophic diabetes, NOS", "Lipoatrophic Diabetes Mellitus", "lipoatrophic diabetes mellitus", "Diabetes mellitus, lipoatrophic", "Diabetes Mellitus, Lipoatrophic", "Lipoatrophic diabetes (disorder)", "Lipoatrophic diabetes (diagnosis)", "diabetes mellitus due to genetic defect in insulin action lipoatrophic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lipoatrophic diabetes", "shortest_name_length": 20}
{"curie": "UMLS:C2984535", "names": ["Stage IV Gallbladder Cancer", "Stage IV Gallbladder Cancer AJCC v6", "Gallbladder Cancer Stage IV AJCC v6", "Gallbladder Carcinoma Stage IV AJCC v6", "Stage IV Gallbladder Carcinoma AJCC v6", "Stage IV Carcinoma of Gallbladder AJCC v6", "Stage IV Carcinoma of the Gallbladder AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Gallbladder Cancer AJCC v6", "shortest_name_length": 27}
{"curie": "MONDO:0009461", "names": ["SPGF5", "macrozoospermia", "SPERMATOGENIC FAILURE 5", "spermatogenic failure 5", "spermatogenic failure type 5", "Macrocephalic sperm head syndrome", "macrocephalic sperm head syndrome", "Male infertility due to macrozoospermia", "male infertility due to macrozoospermia", "infertility associated with multitailed spermatozoa and excessive DNA", "INFERTILITY ASSOCIATED WITH MULTITAILED SPERMATOZOA AND EXCESSIVE DNA", "Infertility Associated with Multi-Tailed Spermatozoa and Excessive DNA", "infertility associated with multi-tailed spermatozoa and excessive DNA", "Infertility associated with multi-tailed spermatozoa and excessive DNA", "Male Infertility with Large-Headed, Multiflagellar, Polyploid Spermatozoa", "male infertility due to large-headed multiflagellar polyploid spermatozoa", "Male infertility due to large-headed multiflagellar polyploid spermatozoa", "male infertility with large-headed, multiflagellar, polyploid spermatozoa", "MALE INFERTILITY WITH LARGE-HEADED, MULTIFLAGELLAR, POLYPLOID SPERMATOZOA", "Infertility associated with multi-tailed spermatozoa and excessive deoxyribonucleic acid", "Infertility associated with multi-tailed spermatozoa and excessive deoxyribonucleic acid (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 5", "shortest_name_length": 5}
{"curie": "MONDO:0001228", "names": ["conjunctival folliculosis", "Conjunctival folliculosis", "Conjunctival folliculosis NOS", "Conjunctival folliculosis, NOS", "conjunctivitis acute follicular", "acute follicular conjunctivitis", "Acute follicular conjunctivitis", "Acute follicular conjunctivitis, NOS", "Acute follicular conjunctivitis (disorder)", "acute follicular conjunctivitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "conjunctival folliculosis", "shortest_name_length": 25}
{"curie": "UMLS:C4524146", "names": ["Eosinophilic pleural effusion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eosinophilic pleural effusion", "shortest_name_length": 29}
{"curie": "MONDO:0043317", "names": ["ADM", "Amyopathic dermatomyositis", "amyopathic dermatomyositis", "Dermatomyositis sine myositis", "dermatomyositis sine myositis", "dermatomyositis without myopathy", "Dermatomyositis sine myositis (disorder)", "dermatomyositis without myopathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyopathic dermatomyositis", "shortest_name_length": 3}
{"curie": "MONDO:0004668", "names": ["Fasciolosis", "fasciolosis", "Fascioliases", "Liver flukes", "Fascioliasis", "fascioliasis", "liver flukes", "FASCIOLIASIS", "Liver flukes NOS", "Fasciola Infection", "Infection, Fasciola", "Fasciola Infections", "liver; fluke disease", "fluke disease; liver", "Infections, Fasciola", "Fasciola; infestation", "infection by fasciola", "infestation; Fasciola", "Infection by Fasciola", "Liver fluke infection", "fascioliasis (diagnosis)", "Sheep liver fluke disease", "Infection by Fasciola, NOS", "Sheep liver fluke infection", "Fasciola hepatica infection", "fasciola hepatica infection", "sheep liver fluke infection", "liver; disease, fluke, sheep", "Infection caused by Fasciola", "infection; sheep liver fluke", "sheep liver fluke; infection", "fasciola hepatica infections", "Infection by Fasciola hepatica", "infestation; Distoma hepaticum", "Distoma hepaticum; infestation", "fluke; infestation, sheep liver", "infestation; fluke, sheep liver", "Liver fluke infection (disorder)", "fluke; infestation, liver (sheep)", "infestation; fluke, liver (sheep)", "Infection due to Fasciola hepatica", "Fasciola hepatica infection (disorder)", "Infection caused by Fasciola (disorder)", "disease (or disorder); liver, fluke, sheep", "fascioliasis due to infection by Fasciola hepatica", "fascioliasis due to infection by Fasciola hepatica (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fascioliasis", "shortest_name_length": 11}
{"curie": "MONDO:0012121", "names": ["OTSC5", "Otosclerosis 5", "otosclerosis 5", "OTOSCLEROSIS 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "otosclerosis 5", "shortest_name_length": 5}
{"curie": "MONDO:0002822", "names": ["trabecular carcinoma", "Trabecular Carcinoma", "Trabecular carcinoma", "Merkel cell carcinoma", "trabecula adenocarcinoma", "Trabecular Adenocarcinoma", "Trabecular adenocarcinoma", "trabecular adenocarcinoma", "trabecular adenocarcinoma (diagnosis)", "Trabecular adenocarcinoma (morphologic abnormality)", "trabecular adenocarcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trabecular adenocarcinoma", "shortest_name_length": 20}
{"curie": "MONDO:0013687", "names": ["SCAR12", "autosomal recessive spinocerebellar ataxia 12", "spinocerebellar ataxia, autosomal recessive 12", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12", "autosomal recessive spinocerebellar ataxia type 12", "Autosomal recessive spinocerebellar ataxia type 12", "spinocerebellar ataxia, autosomal recessive type 12", "spinocerebellar ataxia with mental retardation and epilepsy", "SPINOCEREBELLAR ATAXIA WITH MENTAL RETARDATION AND EPILEPSY", "spinocerebellar ataxia with intellectual disability and epilepsy", "WWOX autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome", "WWOX autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome", "Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to WWOX deficiency", "Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX deficiency", "autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome caused by mutation in WWOX", "autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome due to WWOX deficiency", "autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome caused by mutation in WWOX", "autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WW domain containing oxidoreductase deficiency", "Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WW domain containing oxidoreductase deficiency", "Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX (WW domain containing oxidoreductase) deficiency", "Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WW domain containing oxidoreductase deficiency (disorder)", "autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WW domain containing oxidoreductase deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive spinocerebellar ataxia 12", "shortest_name_length": 6}
{"curie": "UMLS:C5239076", "names": ["Unresectable Epithelioid Hemangioendothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Epithelioid Hemangioendothelioma", "shortest_name_length": 45}
{"curie": "UMLS:C5419571", "names": ["Recurrent Plasma Cell Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Plasma Cell Neoplasm", "shortest_name_length": 30}
{"curie": "MONDO:0006975", "names": ["Smooth muscle tumor", "Smooth Muscle Tumor", "smooth muscle tumor", "muscle smooth tumor", "smooth muscle tumors", "Smooth muscle tumors", "Smooth Muscle Tumors", "Tumor, Smooth Muscle", "Smooth muscle tumour", "Muscle Tumor, Smooth", "Smooth muscle--Tumors", "Tumors, Smooth Muscle", "Muscle Tumors, Smooth", "Tumor of Smooth Muscle", "tumor of smooth muscle", "Smooth Muscle Neoplasm", "smooth muscle neoplasm", "Smooth muscle tumor NOS", "Smooth muscle tumor, NOS", "Smooth muscle tumour NOS", "Neoplasm of Smooth Muscle", "neoplasm of smooth muscle", "Smooth muscle tumour, NOS", "Tumor of the Smooth Muscle", "tumor of the smooth muscle", "neoplasm of the smooth muscle", "Neoplasm of the Smooth Muscle", "Smooth muscle tumor (morphologic abnormality)", "Smooth muscle tumor of uncertain malignant potential", "Smooth muscle tumour of uncertain malignant potential"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "smooth muscle tumor", "shortest_name_length": 19}
{"curie": "MONDO:0030535", "names": ["EBS2D", "epidermolysis bullosa simplex 2d, generalized, intermediate or severe, autosomal recessive", "EPIDERMOLYSIS BULLOSA SIMPLEX 2D, GENERALIZED, INTERMEDIATE OR SEVERE, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolysis bullosa simplex 2d, generalized, intermediate or severe, autosomal recessive", "shortest_name_length": 5}
{"curie": "MONDO:0004781", "names": ["AMI", "ami", "acute MI", "Acute MI", "acute mi", "MI, ACUTE", "MYOCARDIAL INFARCTION ACUTE", "Acute Myocardial Infarction", "Infarction;myocardial;acute", "Acute myocardial infarction", "Myocardial infarction acute", "acute myocardial infarction", "MYOCARDIUM, INFARCTION, ACUTE", "Acute myocardial infarction NOS", "acute myocardial infarction (MI)", "MI - Acute myocardial infarction", "Acute myocardial infarction, NOS", "AMI - Acute myocardial infarction", "Myocardial infarction (acute) NOS", "acute myocardial infarction (disease)", "Acute myocardial infarction (disorder)", "myocardial infarction (disease), acute", "acute myocardial infarction (diagnosis)", "Acute myocardial infarction, unspecified", "Acute myocardial infarction, unspecified site", "Acute myocardial infarction, unspecified site, episode of care unspecified", "Acute myocardial infarction of unspecified site, episode of care unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myocardial infarction", "shortest_name_length": 3}
{"curie": "MONDO:0060589", "names": ["FPVEPD", "FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION", "facial palsy, congenital, with ptosis and velopharyngeal dysfunction", "facial palsy, congenitla, with ptosis and velopharyngeal dysfunction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "facial palsy, congenital, with ptosis and velopharyngeal dysfunction", "shortest_name_length": 6}
{"curie": "MONDO:0006249", "names": ["HP", "MP", "Hyperplasic polyp", "hyperplasic polyp", "Metaplastic Polyp", "Metaplastic polyp", "metaplastic polyp", "hyperplasic polyps", "POLYP HYPERPLASTIC", "Hyperplastic Polyp", "hyperplastic polyp", "metaplastic polyps", "Hyperplastic polyp", "Hyperplastic polyps", "hyperplastic polyps", "Metaplastic polyp (morphologic abnormality)", "Hyperplastic polyp (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperplastic polyp", "shortest_name_length": 2}
{"curie": "UMLS:C1336156", "names": ["stage IIA breast cancer", "breast cancer stage IIA", "Breast Cancer Stage IIA", "Stage IIA Breast Cancer", "Stage IIA Breast Carcinoma", "Breast Carcinoma Stage IIA", "stage IIA breast carcinoma", "breast carcinoma stage IIA", "stage IIA breast cancer AJCC v7", "Stage IIA Breast Cancer AJCC v6", "Stage IIA Breast Cancer AJCC v7", "Stage IIA Breast Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Breast Carcinoma", "shortest_name_length": 23}
{"curie": "MONDO:0008505", "names": ["SGP75", "SURFACE GLYCOPROTEIN 75", "surface glycoprotein 75", "SURFACE ANTIGEN, GLYCOPROTEIN 75", "surface antigen, glycoprotein 75", "surface antigen, glycoprotein type 75"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "surface antigen, glycoprotein 75", "shortest_name_length": 5}
{"curie": "UMLS:C0267953", "names": ["necrosis pancreas", "pancreas necrosis", "necrosis; pancreas", "pancreas; necrosis", "pancreatic necrosis", "Pancreatic necrosis", "necrosis of pancreas", "Necrosis of pancreas", "Pancreatic necrosis NOS", "Pancreatic Necrotic Lesion", "pancreatic necrosis (diagnosis)", "Necrosis of pancreas (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Necrosis of pancreas", "shortest_name_length": 17}
{"curie": "UMLS:C4727071", "names": ["Advanced Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Lymphoma", "shortest_name_length": 17}
{"curie": "UMLS:C0267465", "names": ["Enterostenosis", "enterostenosis", "bowel; stenosis", "stenosis; bowel", "Enterostenosis NOS", "INTESTINAL STENOSIS", "Stenosis intestinal", "STENOSIS INTESTINAL", "Intestinal stenosis", "intestine stricture", "intestinal stenosis", "Intestinal Stricture", "intestinal stricture", "Intestinal stricture", "STRICTURE INTESTINAL", "stricture intestinal", "Stricture intestinal", "Stenosis of intestine", "stenosis of intestine", "Stricture of Intestine", "Stricture of intestine", "Intestinal stenosis NOS", "Intestinal stricture NOS", "enterostenosis (diagnosis)", "Stenosis of intestine or colon", "Stricture of intestine or colon", "intestinal stenosis (diagnosis)", "Stenosis of intestine (disorder)", "Stricture of intestine (disorder)", "Stenosis of colon or intestine NOS", "Stricture of colon or intestine NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stenosis of intestine", "shortest_name_length": 14}
{"curie": "UMLS:C4526585", "names": ["Stage II Thymus Epithelial Neoplasm", "Stage II Thymic Epithelial Neoplasm AJCC v8", "Stage II Thymus Epithelial Neoplasm AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Thymic Epithelial Neoplasm AJCC v8", "shortest_name_length": 35}
{"curie": "UMLS:C4054743", "names": ["IgM - Associated Nephropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IgM - Associated Nephropathy", "shortest_name_length": 28}
{"curie": "UMLS:C1333058", "names": ["Classic Type Atypical Fibroxanthoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Classic Type Atypical Fibroxanthoma", "shortest_name_length": 35}
{"curie": "MONDO:0033885", "names": ["mitochondrial complex IV deficiency, nuclear-type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex IV deficiency, nuclear-type", "shortest_name_length": 49}
{"curie": "MONDO:0001911", "names": ["tracheal calcification", "Tracheal Calcification", "trachea; calcification", "Tracheal calcification", "Trachea calcifications", "calcification; trachea", "Tracheal calcifications", "Calcification of trachea", "calcification of trachea", "Calcification of the trachea", "Tracheal ectopic calcification", "tracheal calcification (diagnosis)", "Calcification of trachea (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tracheal calcification", "shortest_name_length": 22}
{"curie": "UMLS:C1411873", "names": ["Ovulation disorder", "disorder; ovulation", "ovulation; disorder", "disturbance; ovulation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovulation disorder", "shortest_name_length": 18}
{"curie": "MONDO:0018939", "names": ["MEB", "MEB syndrome", "santavuori syndrome", "Santavuori syndrome", "Muscle eye brain disease", "Muscle Eye Brain Disease", "Muscle-eye-brain disease", "muscle eye brain disease", "muscle-eye-brain disease", "Muscle-Eye-Brain Disease", "muscle-eye-brain syndrome", "Muscle-eye-brain syndrome", "Muscle-Eye-Brain Diseases", "muscle-eye-brain (MEB) disease", "MEB (Muscle-Eye-Brain) Syndrome", "muscle-eye-brain syndrome (MEBS)", "Muscle eye brain disease (disorder)", "Santavuori congenital muscular dystrophy", "muscular dystrophy-dystroglycanopathy congenital with brain and eye anomalies A3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscle-eye-brain disease", "shortest_name_length": 3}
{"curie": "MONDO:0019573", "names": ["ARCL2", "autosomal recessive cutis laxa type 2", "cutis laxa with joint laxity and developmental delay"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive cutis laxa type 2", "shortest_name_length": 5}
{"curie": "MONDO:0000859", "names": ["spina bifida occult", "Closed spina bifida", "closed spina bifida", "occult spina bifida", "Occult Spina Bifida", "Closed Spinal Bifida", "spina bifida occulta", "Spina bifida occulta", "Spina Bifida Occulta", "bifida occults spina", "bifida occulta spina", "SPINA BIFIDA OCCULTA", "Spina Bifida, Occult", "occulta; spina bifida", "spina bifida; occulta", "Spinal Bifida, Closed", "Cryptomerorachischisis", "SBO - Spina bifida occulta", "spina bifida occulta (disease)", "Spina bifida occulta (disorder)", "spina bifida occulta (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spina bifida occulta", "shortest_name_length": 19}
{"curie": "UMLS:C5204276", "names": ["Acute Bilineal Leukemia in Remission"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Bilineal Leukemia in Remission", "shortest_name_length": 36}
{"curie": "MONDO:0006335", "names": ["endometrioid ovarian cancer", "Ovarian Endometrioid Cancer", "ovarian endometrioid cancer", "endometrioid ovary carcinoma", "endometrioid cancer of ovary", "endometrioid carcinoma ovary", "Endometrioid carcinoma ovary", "Endometrioid Cancer of Ovary", "ovarian endometrioid carcinoma", "Ovarian Endometrioid Carcinoma", "Ovarian endometrioid carcinoma", "Endometrioid Carcinoma of Ovary", "Endometrioid carcinoma of ovary", "endometrioid carcinoma of ovary", "ovary endometrium adenocarcinoma", "Endometrioid Cancer of the Ovary", "endometrioid cancer of the ovary", "endometrioid carcinoma of the ovary", "endometrium adenocarcinoma of ovary", "Ovarian Endometrioid Adenocarcinoma", "Endometrioid Carcinoma of the Ovary", "ovarian endometrioid adenocarcinoma", "endometrioid adenocarcinoma of ovary", "Endometrioid Adenocarcinoma of Ovary", "Ovarian Endometrioid Adenocarcinoma NOS", "Endometrioid carcinoma ovary (disorder)", "ovarian malignant carcinoma endometrioid", "endometrioid adenocarcinoma of the ovary", "Endometrioid Adenocarcinoma of the Ovary", "adenocarcinoma of the ovary, endometrioid", "ovary cancer, endometrioid adenocarcinoma", "endometrioid carcinoma of ovary (diagnosis)", "ovarian cancer, endometrioid adenocarcinoma", "endometrioid adenocarcinoma of ovary (diagnosis)", "Ovarian Endometrioid Adenocarcinoma not Otherwise Specified", "Ovarian Endometrioid Adenocarcinoma Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian endometrioid adenocarcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C3472181", "names": ["Severe dehydration", "Severe dehydration (disorder)", "Severe dehydration (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Severe dehydration", "shortest_name_length": 18}
{"curie": "UMLS:C0877153", "names": ["Neutropenic sepsis", "neutropenic sepsis", "Neutropenic sepsis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neutropenic sepsis", "shortest_name_length": 18}
{"curie": "UMLS:C1335486", "names": ["Primary Intraosseous Squamous Cell Carcinoma-Solid Type", "Primary Intraosseous Squamous Cell Carcinoma Arising de novo"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Intraosseous Squamous Cell Carcinoma-Solid Type", "shortest_name_length": 55}
{"curie": "MONDO:0016332", "names": ["hypertrophic cardiomyopathy due to intensive athletic training"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophic cardiomyopathy due to intensive athletic training", "shortest_name_length": 62}
{"curie": "UMLS:C0153898", "names": ["Monocytic Leukemia in Remission", "Monocytic Leukemia (in Remission)", "Acute Monocytic Leukemia in Remission", "leukemia monocytic acute in remission", "Acute monocytic leukemia in remission", "Acute monocytic leukemia,in remission", "acute monocytic leukemia in remission", "Acute monocytic leukaemia in remission", "Acute monocytic leukemia, in remission", "Acute Monocytic Leukemia (in Remission)", "Acute monocytic leukemia (in remission)", "Acute monocytic leukaemia, in remission", "Acute monocytic leukaemia (in remission)", "Acute monocytic leukemia in remission (disorder)", "acute monocytic leukemia in remission (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute monocytic leukemia in remission", "shortest_name_length": 31}
{"curie": "MONDO:0012658", "names": ["BDB2", "Brachydactyly type B2", "brachydactyly type B2", "BRACHYDACTYLY, TYPE B2", "Brachydactyly, Type B2", "brachydactyly, type B2", "Brachydactyly type B2 (disorder)", "BRACHYDACTYLY, TYPE B2 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly type B2", "shortest_name_length": 4}
{"curie": "MONDO:0009110", "names": ["DCBXA", "Dicarboxylicaminoaciduria", "dicarboxylic aminoaciduria", "Dicarboxylicamino Aciduria", "DICARBOXYLIC AMINOACIDURIA", "Dicarboxylic aminoaciduria", "Dicarboxylic amino aciduria", "Dicarboxylic aminoaciduria syndrome", "glutamate-aspartate Transport defect", "Glutamate-Aspartate Transport Defect", "Glutamate aspartate transport defect", "glutamate-aspartate transport defect", "GLUTAMATE-ASPARTATE TRANSPORT DEFECT", "Glutamate-aspartate transport defect", "Glutamate and aspartate transport defect", "Dicarboxylic aminoaciduria syndrome (disorder)", "Inborn error of glutamic and aspartate transport"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dicarboxylic aminoaciduria", "shortest_name_length": 5}
{"curie": "UMLS:C3273223", "names": ["Periosteal Desmoid Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Periosteal Desmoid Tumor", "shortest_name_length": 24}
{"curie": "UMLS:C1336526", "names": ["Anaplastic Carcinoma of Submandibular Gland", "Submandibular Gland Undifferentiated Carcinoma", "Anaplastic Carcinoma of the Submandibular Gland", "Undifferentiated Carcinoma of Submandibular Gland", "Undifferentiated Carcinoma of the Submandibular Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Submandibular Gland Undifferentiated Carcinoma", "shortest_name_length": 43}
{"curie": "UMLS:C1297955", "names": ["neoplasm of seminal vesicle secondary", "Secondary malignant neoplasm of seminal vesicle", "Metastatic malignant neoplasm of seminal vesicle", "Metastatic malignant neoplasm to seminal vesicle", "Metastatic Malignant Neoplasm in the Seminal Vesicle", "Secondary malignant neoplasm of seminal vesicle (diagnosis)", "Metastatic malignant neoplasm to seminal vesicle (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to seminal vesicle", "shortest_name_length": 37}
{"curie": "MONDO:0009984", "names": ["senile retinitis pigmentosa", "Retinitis Pigmentosa, Senile", "retinitis pigmentosa, 'Senile'", "RETINITIS PIGMENTOSA, 'SENILE'", "late-adult onset retinitis pigmentosa", "retinitis pigmentosa, late-ADULT onset", "RETINITIS PIGMENTOSA, LATE-ADULT ONSET", "Retinitis Pigmentosa, Late-Adult Onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "late-adult onset retinitis pigmentosa", "shortest_name_length": 27}
{"curie": "UMLS:C1333866", "names": ["Grade I Colon Adenocarcinoma", "Grade 1 Colon Adenocarcinoma", "Well Differentiated Colon Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade 1 Colon Adenocarcinoma", "shortest_name_length": 28}
{"curie": "UMLS:C4726566", "names": ["Extracranial Solid Tumor", "Extracranial Solid Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extracranial Solid Neoplasm", "shortest_name_length": 24}
{"curie": "UMLS:C0156146", "names": ["Regional enteritis", "small intestine; Crohn", "Crohn; small intestine", "Granulomatous enteritis", "RE - regional enteritis", "Crohn's regional enteritis", "Crohns disease, small intestine", "Crohn Disease of Small Intestine", "Crohn disease of small intestine", "Regional enteritis of small bowel", "CROHNS DISEASE OF SMALL INTESTINE", "Crohn's Disease of Small Intestine", "Crohn's disease of small intestine", "Terminal ileitis of small intestine", "regional enteritis; small intestine", "small intestine; regional enteritis", "Regional ileitis of small intestine", "Segmental ileitis of small intestine", "Regional enteritis of small intestine", "Crohn's disease of small intestine (disorder)", "Crohn's disease of small intestine (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Crohn's disease of small intestine", "shortest_name_length": 18}
{"curie": "MONDO:0013932", "names": ["CG5", "CGF", "CG10", "PBD5A", "Peroxisome Biogenesis Disorder 5A", "peroxisome biogenesis disorder 5A", "peroxisome biogenesis disorder 5A (Zellweger)", "PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)", "peroxisome biogenesis disorder, complementation group F", "PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP F", "peroxisome biogenesis disorder, complementation group 5", "PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 5", "PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 10", "peroxisome biogenesis disorder, complementation group 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder 5A (Zellweger)", "shortest_name_length": 3}
{"curie": "MONDO:0006909", "names": ["Dwarf, asexual", "Pituitary dwarf", "Paltauf's dwarf", "pituitary dwarf", "dwarfs pituitary", "Asexual dwarfism", "Pituitary Nanism", "Pituitary nanism", "Lorain; dwarfism", "Burnier syndrome", "dwarfism; Lorain", "Levi-Lorain dwarf", "Nanism, Pituitary", "Dwarf, Brissaud's", "Frohlich dwarfism", "hypophyseal dwarf", "Brissaud dwarfism", "pituitary dwarfism", "Nebecourt syndrome", "Pituitary dwarfism", "Pituitary Dwarfism", "Dwarf, hypophyseal", "PITUITARY DWARFISM", "dwarfism pituitary", "dwarfism; pituitary", "Prepuberal dwarfism", "Dwarfism, Pituitary", "Dwarfism, pituitary", "pituitary; dwarfism", "Lorain-Levi dwarfism", "Prepubertal dwarfism", "Dwarfism (Pituitary)", "Lorain - Levi dwarfism", "hypopituitary dwarfism", "Isolated GH Deficiency", "Hypopituitary dwarfism", "Brissaud-Meige syndrome", "Isolated HGH Deficiency", "Hypophyseal infantilism", "Lorain-Levi short stature", "Hyposomatotropic dwarfism", "Isolated deficiency of HGH", "Hyposomatotrophic Dwarfism", "short; stature, hypophyseal", "Asexual dwarfism (disorder)", "stature; short, hypophyseal", "short; stature, Lorain-Levi", "stature; short, Lorain-Levi", "Pituitary dwarfism (disorder)", "Isolated Somatotropin Deficiency", "Isolated somatotropin deficiency", "Isolated growth hormone deficiency", "Isolated Growth Hormone Deficiency", "Growth Hormone Deficiency Dwarfism", "Dwarfism, Growth Hormone Deficiency", "Isolated deficiency of growth hormone", "Isolated Human Growth Hormone Deficiency", "Isolated Somatotropin Deficiency Disorder", "Isolated deficiency of human growth hormone", "Isolated deficiency of growth hormone in children", "Hypopituitary dwarfism with failure of development of sexual characteristics"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pituitary dwarfism", "shortest_name_length": 14}
{"curie": "MONDO:0010294", "names": ["XLN", "Xln", "SCNX", "severe congenital neutropenia X-linked", "X-linked severe congenital neutropenia", "severe congenital neutropenia, X-linked", "Neutropenia, Severe Congenital, X-Linked", "NEUTROPENIA, SEVERE CONGENITAL, X-LINKED", "neutropenia, severe congenital, X-linked", "Severe neutropenia - congenital X-Linked", "X-linked severe congenital neutropenia (disorder)", "X-linked severe congenital neutropenia (diagnosis)", "neutropenia, severe congenital, X-linked, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked severe congenital neutropenia", "shortest_name_length": 3}
{"curie": "MONDO:0015434", "names": ["R18", "Ring 18", "r(18) syndrome", "ring 18 syndrome", "18 ring syndrome", "Ring chromosome 18", "Ring Chromosome 18", "ring chromosome 18", "chromosome 18 ring", "Chromosome 18 ring", "Ring chromosome type 18", "Ring Chromosome 18 Syndrome", "Ring chromosome 18 syndrome", "ring 18 chromosome syndrome", "chromosome 18 ring syndrome", "Ring chromosome 18 syndrome (disorder)", "Ring chromosome 18 syndrome (diagnosis)", "anomaly of chromosome pair ring 18 syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ring chromosome 18", "shortest_name_length": 3}
{"curie": "UMLS:C0741165", "names": ["AORTA EMBOLI", "aortic embolus", "Aortic embolus", "embolus aortic", "aorta; embolism", "embolism; aortic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aortic embolus", "shortest_name_length": 12}
{"curie": "UMLS:C4042763", "names": ["Residual Block", "Residual Blocks", "Block, Residual", "Blocks, Residual", "Residual Neuromuscular Block", "Neuromuscular Block, Residual", "Residual Neuromuscular Blocks", "Block, Residual Neuromuscular", "Blocks, Residual Neuromuscular", "Neuromuscular Blocks, Residual", "Residual Neuromuscular Blockade", "Postoperative Residual Weakness", "Weakness, Postoperative Residual", "Residual Weakness, Postoperative", "Residual Neuromuscular Blockades", "Neuromuscular Blockade, Residual", "Blockade, Residual Neuromuscular", "Postoperative Residual Weaknesses", "Blockades, Residual Neuromuscular", "Neuromuscular Blockades, Residual", "Residual Weaknesses, Postoperative", "Weaknesses, Postoperative Residual", "Postoperative Residual Curarisation", "Postoperative Residual Curarization", "Postoperative Residual Curarisations", "Residual Curarisation, Postoperative", "Curarization, Postoperative Residual", "Postoperative Residual Curarizations", "Residual Curarization, Postoperative", "Residual Curarizations, Postoperative", "Residual Curarisations, Postoperative", "Curarizations, Postoperative Residual"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postoperative Residual Curarization", "shortest_name_length": 14}
{"curie": "MONDO:0030353", "names": ["JBTS38", "JOUBERT SYNDROME 38", "Joubert syndrome 38"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome 38", "shortest_name_length": 6}
{"curie": "MONDO:0012898", "names": ["NRCLP4", "narcolepsy 4", "narcolepsy 4, susceptibility to", "NARCOLEPSY 4, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "narcolepsy 4, susceptibility to", "shortest_name_length": 6}
{"curie": "MONDO:0030436", "names": ["SIDBA5", "anemia, sideroblastic, 5", "ANEMIA, SIDEROBLASTIC, 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anemia, sideroblastic, 5", "shortest_name_length": 6}
{"curie": "MONDO:0001151", "names": ["Benign Essential Hypertension", "essential benign hypertension", "benign essential hypertension", "Benign essential hypertension", "Essential hypertension, benign", "Benign essential hypertension (disorder)", "benign essential hypertension (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign essential hypertension", "shortest_name_length": 29}
{"curie": "UMLS:C1332235", "names": ["Alkylating Agent Related Myelodysplastic Syndrome", "Alkylating Agent-Related Myelodysplastic Syndrome", "Therapy-related myelodysplastic syndrome, alkylating agent related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alkylating Agent-Related Myelodysplastic Syndrome", "shortest_name_length": 49}
{"curie": "MONDO:0000088", "names": ["Early puberty", "early puberty", "puberty early", "Sexual precocity", "sexual precocity", "Pubertas praecox", "SEXUAL PRECOCITY", "pubertas praecox", "Sexual Precocity", "Pubertas Praecox", "Premature puberty", "Praecox, Pubertas", "premature puberty", "premature; puberty", "puberty; premature", "PRECOCIOUS PUBERTY", "puberty precocious", "Precocious puberty", "Puberty;precocious", "Puberty precocious", "precocious puberty", "PUBERTY PRECOCIOUS", "Precocious Puberty", "Early-onset puberty", "Puberty, Precocious", "Early onset puberty", "precocious; puberty", "puberty; precocious", "Precocious Puberties", "Sexual precocity NOS", "Sexual precocity, NOS", "Puberties, Precocious", "Precocious puberty NOS", "Early onset of puberty", "True precocious puberty", "true precocious puberty", "Precocious true puberty", "MATURATION SEX ACCELERATED", "Maturation sex accelerated", "familial precocious puberty", "Accelerated sexual maturity", "idiopathic sexual precocity", "ACCELERATED SEXUAL MATURITY", "Accelerated sexual maturation", "precocious sexual development", "Precocious sexual development", "Precocious puberty (disorder)", "precocious puberty (diagnosis)", "Abnormally early onset of puberty"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "precocious puberty", "shortest_name_length": 13}
{"curie": "MONDO:0016102", "names": ["SIDP", "Subacute inflammatory demyelinating polyneuropathy", "subacute inflammatory demyelinating polyneuropathy", "Subacute idiopathic demyelinating polyradiculoneuropathy", "subacute inflammatory demyelinating polyradiculoneuropathy", "Subacute inflammatory demyelinating polyradiculoneuropathy", "Subacute inflammatory demyelinating polyradiculoneuropathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subacute inflammatory demyelinating polyneuropathy", "shortest_name_length": 4}
{"curie": "MONDO:0003361", "names": ["Small Bowel Sarcoma", "small bowel sarcoma", "Sarcoma of Small Bowel", "sarcoma of small bowel", "Small Intestine Sarcoma", "small intestine sarcoma", "small intestinal sarcoma", "Small Intestinal Sarcoma", "Sarcoma, Small Intestinal", "sarcoma, small intestinal", "Sarcoma of the Small Bowel", "Sarcoma of Small Intestine", "sarcoma of the small bowel", "sarcoma of small intestine", "sarcoma of the small intestine", "sarcoma of the Small Intestine", "Sarcoma of the Small Intestine", "sarcoma of small intestine (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small intestinal sarcoma", "shortest_name_length": 19}
{"curie": "UMLS:C1710624", "names": ["Venous Angiomyoma", "Venous Angioleiomyoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Venous Angioleiomyoma", "shortest_name_length": 17}
{"curie": "UMLS:C0428981", "names": ["PNC", "AV junctional beats", "A-V junctional beats", "Junctional Extra Beat", "junctional premature beat", "Premature nodal contraction", "extrasystoles; AV-junctional", "Junctional premature complex", "Junctional Premature Complex", "premature junctional complex", "JUNCTIONAL PREMATURE COMPLEX", "AV-junctional; extrasystoles", "Junctional Premature Complexes", "atrioventricular junctional beats", "premature junctional complex (PJC)", "Junctional premature depolarisation", "premature depolarization junctional", "junctional premature depolarization", "Junctional premature depolarization", "AV junctional (nodal) premature beats", "Junctional premature complex (disorder)", "Junctional Premature Complex by ECG Finding", "Junctional Premature Complex by EKG Finding", "atrioventricular junctional beats (diagnosis)", "junctional premature depolarization (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Junctional premature complex (disorder)", "shortest_name_length": 3}
{"curie": "MONDO:0004858", "names": ["gallbladder; occlusion", "occlusion; gallbladder", "Gallbladder Obstruction", "Gallbladder obstruction", "gallbladder obstruction", "obstruction; gallbladder", "occlusion of gallbladder", "gallbladder; obstruction", "Occlusion of gallbladder", "obstruction of gallbladder", "Obstruction of gallbladder", "gallbladder obstruction (diagnosis)", "Occlusion of gallbladder (disorder)", "Obstruction of gallbladder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "occlusion of gallbladder", "shortest_name_length": 22}
{"curie": "MONDO:0044778", "names": ["NLPHL", "Hodgkin lymphoma nodular LP, NOS", "Nodular Sclerosing Hodgkin's Lymphoma", "Hodgkin; lymphocytic predominance, nodular", "Nodular Lymphocyte Predominant Hodgkin Lymphoma", "nodular lymphocyte-predominant Hodgkin lymphoma", "nodular lymphocyte predominant Hodgkin lymphoma", "Nodular lymphocyte predominant Hodgkin lymphoma", "lymphocyte predominant Hodgkin lymphoma, nodular", "Nodular Lymphocyte Predominant Hodgkin's Lymphoma", "Hodgkin lymphoma, lymphocyte predominant, nodular", "Hodgkin Lymphoma, Nodular Lymphocyte Predominance", "Nodular Lymphocyte-Predominant Hodgkin's Lymphoma", "Hodgkin lymphoma, nodular lymphocyte predominance", "nodular lymphocyte predominant Hodgkin's lymphoma", "Hodgkin lymphoma, lymphocyte predominance, nodular", "Hodgkin's disease, lymphocytic predominance, nodular", "Hodgkin's disease, lymphocytic predominance - nodular", "disease; Hodgkin's, lymphocytic predominance, nodular", "Hodgkin lymphoma nodular lymphocyte predominant type, NOS", "Hodgkin lymphoma, nodular lymphocyte predominance (disorder)", "Hodgkin lymphoma, nodular lymphocyte predominance (clinical)", "lymphocyte predominant Hodgkin lymphoma, nodular (diagnosis)", "nodular Hodgkin's disease with lymphocytic-histiocytic predominance", "Hodgkin lymphoma, nodular lymphocyte predominance (morphologic abnormality)", "nodular Hodgkin's disease with lymphocytic-histiocytic predominance (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nodular lymphocyte predominant Hodgkin lymphoma", "shortest_name_length": 5}
{"curie": "MONDO:0007969", "names": ["MRS", "Mros", "MROS", "Melkersson", "MELKERSSON SYNDROME", "melkersson syndrome", "Melkersson syndrome", "Melkersson Syndrome", "Melkersson's syndrome", "melkersson's syndrome", "cheilitis Granulomatosa", "Melkerson-Rosenthal Syndrome", "melkerson rosenthal syndrome", "Rosenthal-Melkerson Syndrome", "Rosenthal Melkerson Syndrome", "melkerson-rosenthal syndrome", "Melkerson Rosenthal Syndrome", "Syndrome, Melkerson Rosenthal", "Melkersson-Rosenthal syndrome", "Rosenthal-Melkersson Syndrome", "Melkersson Rosenthal Syndrome", "melkersson rosenthal syndrome", "Melkersson-Rosenthal Syndrome", "Rosenthal Melkersson Syndrome", "melkersson-rosenthal syndrome", "rosenthal-melkersson syndrome", "MELKERSSON-ROSENTHAL SYNDROME", "Melkersson's syndrome (disorder)", "Melkersson's syndrome (diagnosis)", "Macrocheilia, Facial Palsy, Edema", "Melkersson-Rosenthal-Miescher Syndrome", "Melkersson Rosenthal Miescher Syndrome", "Macrocheilia, facial palsy AND edema syndrome", "Macrocheilia, facial palsy and edema syndrome", "Macrocheilia, facial palsy and oedema syndrome", "Macrocheilia, facial palsy AND oedema syndrome", "Miescher Melkersson Rosenthal Granulomatous Cheilitis", "Miescher-Melkersson-Rosenthal Granulomatous Cheilitis", "Cheilitis, Miescher-Melkersson-Rosenthal Granulomatous", "Granulomatous Cheilitis, Miescher-Melkersson-Rosenthal", "cheilitis granulomatosa of Mescher-Melkersson-Rosenthal", "Cheilitis granulomatosa of Mescher-Melkersson-Rosenthal", "cheilitis granulomatosa of Miescher-Melkersson-Rosenthal", "Cheilitis granulomatosa of Miescher-Melkersson-Rosenthal", "Cheilitis granulomatosis of Miescher-Melkersson Rosenthal", "Facial Neuropathy, Orofacial Edema, Cheilitis Granulomatosa", "Orofacial Edema, Facial Neuropathy, Cheilitis Granulomatosa", "Cheilitis Granulomatosa, Facial Neuropathy, Orofacial Edema", "Facial Neuropathy, Cheilitis Granulomatosa, Orofacial Edema", "Cheilitis Granulomatosa, Orofacial Edema, Facial Neuropathy", "Orofacial Edema, Cheilitis Granulomatosa, Facial Neuropathy", "Cheilitis granulomatosa of Miescher-Melkersson-Rosenthal (disorder)", "cheilitis granulomatosa of Miescher-Melkersson-Rosenthal (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Melkersson-Rosenthal syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0010003", "names": ["Rowley-Rosenberg syndrome", "ROWLEY-ROSENBERG SYNDROME", "Rowley-Rosenberg syndrome (disorder)", "Growth retardation, pulmonary hypertension, and aminoaciduria", "Growth Retardation, Pulmonary Hypertension, and Amino Aciduria", "GROWTH RETARDATION, PULMONARY HYPERTENSION, AND AMINO ACIDURIA", "Growth retardation, pulmonary hypertension, and amino aciduria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rowley-Rosenberg syndrome", "shortest_name_length": 25}
{"curie": "UMLS:C4727398", "names": ["Recurrent Ovarian Clear Cell Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Ovarian Clear Cell Adenocarcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0002104", "names": ["FND", "hysteria", "REACTION CONVERSION", "Conversion neurosis", "Conversion reaction", "conversion reaction", "CONVERSION DISORDER", "conversion neurosis", "Conversion disorder", "Conversion hysteria", "CONVERSION REACTION", "conversion hysteria", "Conversion Hysteria", "Conversion Disorder", "Disorder;conversion", "Conversion Reaction", "Reaction conversion", "Neurosis conversion", "NEUROSIS CONVERSION", "reaction conversion", "hysterical disorder", "conversion disorder", "Conversion Neurosis", "conversion; reaction", "neurosis; conversion", "Hysteria, Conversion", "reaction; conversion", "conversion disorders", "conversions disorder", "conversion; neurosis", "Conversion Disorders", "hysterical conversion", "Conversion disorder, NOS", "HYSTERIA CONVERSION TYPE", "Hysteria conversion type", "functional movement disorder", "Functional Movement Disorder", "Functional Movement Disorders", "Disorder, Functional Movement", "Movement Disorder, Functional", "Conversion Hysterical Neurosis", "Movement Disorders, Functional", "conversion hysterical neurosis", "Psychologic conversion disorder", "conversion disorder (diagnosis)", "conversion hysteria or reaction", "Conversion hysteria or reaction", "functional neurological disorder", "Hysterical Neurosis (Conversion)", "Functional Neurological Disorder", "Functional neurological disorder", "Conversion disorder, psychologic", "Disorder, Functional Neurological", "Functional Neurological Disorders", "Neurological Disorder, Functional", "Neurological Disorders, Functional", "Hysterical neurosis, conversion type", "hysterical neurosis, conversion type", "Psychologic conversion disorder, NOS", "Neurosis, hysterical, conversion type", "Psychologic conversion disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "conversion disorder", "shortest_name_length": 3}
{"curie": "MONDO:0012459", "names": ["HYT6", "Hyt6", "hypertension, essential, susceptibility to, 6", "HYPERTENSION, ESSENTIAL, SUSCEPTIBILITY TO, 6", "hypertension, essential, kidney function-related", "HYPERTENSION, ESSENTIAL, KIDNEY FUNCTION-RELATED", "hypertension, essential, susceptibility to, type 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertension, essential, susceptibility to, 6", "shortest_name_length": 4}
{"curie": "MONDO:0004869", "names": ["PELVIS VARIX", "pelvis; varix", "pelvic varices", "Pelvic varices", "varices; pelvic", "varicose vein pelvic", "Varicose veins pelvic", "pelvic varicose veins", "Varicose veins of pelvis", "pelvic varices (diagnosis)", "Varicose veins of pelvis (disorder)", "pelvic region of trunk varicose disease", "varicose disease of pelvic region of trunk"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pelvic varices", "shortest_name_length": 12}
{"curie": "UMLS:C3472609", "names": ["Mixed acinar-ductal carcinoma", "Pancreatic Mixed Acinar-Ductal Carcinoma", "Mixed Acinar-Ductal Carcinoma of the Pancreas", "Mixed acinar-ductal carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mixed acinar-ductal carcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0002029", "names": ["chronic gonorrhea of cervix", "Gonorrhea of cervix, chronic", "Cervicitis gonococcal chronic", "Chronic gonococcal cervicitis", "chronic gonococcal cervicitis", "Gonococcal cervicitis chronic", "gonococcal cervicitis, chronic", "Gonococcal cervicitis, chronic", "Chronic gonococcal cervicitis (disorder)", "chronic gonococcal cervicitis (diagnosis)", "Gonococcal cervicitis specified as chronic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic gonorrhea of cervix", "shortest_name_length": 27}
{"curie": "UMLS:C4329642", "names": ["Cerebellar Ependymal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebellar Ependymal Tumor", "shortest_name_length": 26}
{"curie": "MONDO:0000540", "names": ["small intestine NET G1", "small intestinal NET G1", "Small Intestinal NET G1", "small bowel carcinoid tumor", "bowel carcinoid small tumor", "Small Bowel Carcinoid Tumor", "intestinal carcinoid tumour", "bowel carcinoid small tumors", "carcinoid tumor of small bowel", "Carcinoid Tumor of Small Bowel", "small intestine carcinoid tumor", "Small Intestine Carcinoid Tumor", "carcinoid intestine small tumor", "carcinoid small intestine tumor", "Small Intestinal Carcinoid Tumor", "small intestinal carcinoid tumor", "carcinoid tumor of small intestine", "carcinoid tumor of the small bowel", "Carcinoid Tumor of Small Intestine", "Carcinoid tumor of small intestine", "Carcinoid Tumor of the Small Bowel", "Carcinoid tumor of the small bowel", "Carcinoid tumour of the small bowel", "Carcinoid tumour of small intestine", "Carcinoid Tumor of the Small Intestine", "carcinoid tumor of the small intestine", "Small Intestinal Neuroendocrine Tumor G1", "small intestinal neuroendocrine tumor G1", "small intestine carcinoid tumor (disease)", "small intestine neuroendocrine neoplasm G1", "Carcinoid tumor of small intestine (disorder)", "small intestine carcinoid neuroendocrine tumor", "grade 1 neuroendocrine neoplasm of small intestine", "small intestine neuroendocrine tumor, well differentiated, low grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small intestinal neuroendocrine tumor G1", "shortest_name_length": 22}
{"curie": "UMLS:C4521810", "names": ["Stage IIB Appendix Cancer", "Stage IIB Appendix Carcinoma AJCC v8", "Stage IIB Appendiceal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Appendix Carcinoma AJCC v8", "shortest_name_length": 25}
{"curie": "UMLS:C0853972", "names": ["Stage IV Inflammatory Breast Cancer", "Inflammatory breast cancer stage IV", "Stage IV Inflammatory Breast Carcinoma", "Stage IV Breast Inflammatory Carcinoma", "Stage IV Breast  Inflammatory Carcinoma", "Inflammatory Carcinoma of Breast Stage IV", "Inflammatory carcinoma of breast stage IV"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Inflammatory carcinoma of breast stage IV", "shortest_name_length": 35}
{"curie": "MONDO:0018614", "names": ["undetermined EOEE", "undetermined early-onset epileptic encephalopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "undetermined early-onset epileptic encephalopathy", "shortest_name_length": 17}
{"curie": "UMLS:C0549322", "names": ["Infection;eyelid", "Eyelid infection", "infection eyelid", "eyelid infection", "EYELID INFECTION", "infection; eyelid", "eye lid infection", "eyelid; infection", "eyelid infections", "eye infection lid", "eye infections lid", "eye infections lids", "Eyelid infection NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eyelid infection", "shortest_name_length": 16}
{"curie": "UMLS:C0271149", "names": ["Secondary angle-closure glaucoma", "secondary angle-closure glaucoma", "Angle-closure glaucoma, secondary", "Glaucoma, angle-closure, secondary", "Secondary angle-closure glaucoma, NOS", "Secondary angle-closure glaucoma (disorder)", "secondary angle-closure glaucoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary angle-closure glaucoma", "shortest_name_length": 32}
{"curie": "MONDO:0010510", "names": ["MRX105", "XLID105", "X-linked mental retardation 105", "MENTAL RETARDATION, X-LINKED 105", "mental retardation, X-linked 105", "intellectual disability, X-linked 105", "mental retardation, X-linked type 105", "intellectual disability, X-linked type 105", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 105", "non-syndromic X-linked intellectual disability 105", "USP27X non-syndromic X-linked intellectual disability", "intellectual developmental disorder, X-linked 105, X-linked recessive", "non-syndromic X-linked intellectual disability caused by mutation in USP27X"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 105", "shortest_name_length": 6}
{"curie": "MONDO:0033312", "names": ["SCZD19", "SCHIZOPHRENIA 19", "schizophrenia 19", "schizophrenia 19, susceptibility to", "schizophrenia 19 with or without an affective disorder", "SCHIZOPHRENIA 19 WITH OR WITHOUT AN AFFECTIVE DISORDER"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schizophrenia 19", "shortest_name_length": 6}
{"curie": "MONDO:0010753", "names": ["XMVD", "CVD1", "EDS 5", "CVDPX", "EDS5, FORMERLY", "congenital valvular dysplasia", "Congenital valvular dysplasia", "Ehlers-Danlos syndrome, type 5", "FLNA-related valvular dystrophy", "CONGENITAL VALVULAR HEART DISEASE", "valvular heart disease, congenital", "Valvular heart disease, congenital", "VALVULAR HEART DISEASE, CONGENITAL", "X-Linked Cardiac Valvular Dysplasia", "X-linked cardiac valvular dysplasia", "Cardiac valvular dysplasia, X-linked", "CARDIAC VALVULAR DYSPLASIA, X-LINKED", "cardiac valvular dysplasia, X-linked", "Congenital dysplasia of cardiac valve", "Dystrophie valvulaire associee a FLNA", "X-Linked Myxomatous Valvular Dysplasia", "MYXOMATOUS VALVULAR DYSTROPHY, X-LINKED", "Myxomatous valvular dystrophy, X-linked", "myxomatous valvular dystrophy, X-linked", "EHLERS-DANLOS SYNDROME, TYPE V, FORMERLY", "Congenital dysplasia of cardiac valve (disorder)", "FLNA-related X-linked myxomatous valvular dysplasia", "Filamin A-Related X-Linked Myxomatous Valvular Dysplasia", "Filamin A-related X-linked myxomatous valvular dysplasia", "Filamin A-related X-linked myxomatous valvular dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiac valvular dysplasia, X-linked", "shortest_name_length": 4}
{"curie": "UMLS:C0274456", "names": ["accidental poison", "accidental poisoning", "Poisoning accidental", "Accidental poisoning", "Poisoning, accidental", "inadvertent poisoning", "Accidental poisoning NOS", "Accidental poisoning (disorder)", "accidental poisoning (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Accidental poisoning NOS", "shortest_name_length": 17}
{"curie": "UMLS:C5237195", "names": ["Unresectable Lung Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Lung Neuroendocrine Neoplasm", "shortest_name_length": 41}
{"curie": "MONDO:0013530", "names": ["ATFB10", "atrial fibrillation familial 10", "atrial fibrillation, familial, 10", "ATRIAL FIBRILLATION, FAMILIAL, 10", "SCN5A familial atrial fibrillation", "atrial fibrillation, familial, type 10", "atrial fibrillation familial 10 (diagnosis)", "familial atrial fibrillation caused by mutation in SCN5A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial fibrillation, familial, 10", "shortest_name_length": 6}
{"curie": "UMLS:C1336012", "names": ["Small Lymphocytic Lymphoma with Plasmacytoid Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Lymphocytic Lymphoma with Plasmacytoid Differentiation", "shortest_name_length": 60}
{"curie": "UMLS:C1332562", "names": ["Bladder Paraganglioma", "Paraganglioma of Bladder", "Paraganglioma of the Bladder", "Urinary Bladder Paraganglioma", "Paraganglioma of Urinary Bladder", "Paraganglioma of the Urinary Bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder Paraganglioma", "shortest_name_length": 21}
{"curie": "UMLS:C0152586", "names": ["Tuberculous Bronchiectasis", "Tuberculous bronchiectasis", "tuberculous bronchiectasis", "bronchiectasis; tuberculous", "Post-tuberculous bronchiectasis", "Tuberculous bronchiectasis (disorder)", "tuberculous bronchiectasis (diagnosis)", "Tuberculous bronchiectasis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tuberculous bronchiectasis", "shortest_name_length": 26}
{"curie": "MONDO:0021667", "names": ["NEURALGIA", "Neuralgia", "neuralgia", "Neurodynia", "neurodynia", "Neuralgias", "neuralgias", "Neurodynias", "pain, nerve", "Neuralgia NOS", "Neuralgia, NOS", "Neuropathic Pain", "sharp nerve pain", "pain, neuropathic", "Pain, Neuropathic", "Neuropathic Pains", "Pains, Neuropathic", "Neuralgia (finding)", "neuralgia (symptom)", "Paroxysmal nerve pain", "neuralgia (diagnosis)", "paroxysmal nerve pain", "Paroxysmal Nerve Pain", "paroxysmal nerve pains", "Pain, Paroxysmal Nerve", "Nerve Pain, Paroxysmal", "Paroxysmal Nerve Pains", "Nerve Pains, Paroxysmal", "Pains, Paroxysmal Nerve"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuralgia", "shortest_name_length": 9}
{"curie": "MONDO:0001443", "names": ["Myringosclerosis", "TYMPANOSCLEROSIS", "tympanosclerosis", "Tympanoscleroses", "Tympanosclerosis", "Myringoscleroses", "SCLEROSIS, TYMPANIC", "TS - Tympanosclerosis", "Tympanosclerosis, NOS", "Tympanic calcification", "Tympanic Calcification", "Calcification, Tympanic", "Tympanosclerosis syndrome", "Tympanosclerosis (disorder)", "tympanosclerosis (diagnosis)", "Tympanosclerosis, unspecified ear", "Tympanosclerosis, unspecified as to involvement", "Tympanosclerosis involving other combination of structures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tympanosclerosis", "shortest_name_length": 16}
{"curie": "UMLS:C0333887", "names": ["Severe urothelial cell atypia", "Severe transitional cell atypia", "Severe Transitional Cell Atypia", "Severe transitional cell atypia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Severe transitional cell atypia", "shortest_name_length": 29}
{"curie": "UMLS:C5237384", "names": ["Refractory Bladder Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Bladder Urothelial Carcinoma", "shortest_name_length": 39}
{"curie": "MONDO:0000709", "names": ["ileitis", "Ileitis", "ILEITIS", "Ileitis NOS", "Ileitis, NOS", "Crohn Ileitis", "Crohn ileitis", "crohn's ileitis", "Crohn's ileitis", "Crohn's Ileitis", "Regional ileitis", "ILEITIS REGIONAL", "Regional Ileitis", "Ileitis regional", "regional ileitis", "ileitis; regional", "Ileitis, regional", "regional; ileitis", "Ileitis (disorder)", "ileitis (regional)", "inflammation; ileum", "ileitis (diagnosis)", "ileum; inflammation", "Crohn disease of ileum", "Crohn's disease of ileum", "Inflammation of the ileum", "Crohn's disease of the ileum", "Crohn's disease of ileum (disorder)", "Crohn's disease of ileum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Crohn ileitis", "shortest_name_length": 7}
{"curie": "UMLS:C4331473", "names": ["Unresectable Digestive System Adenocarcinoma", "Unresectable Gastrointestinal System Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Digestive System Adenocarcinoma", "shortest_name_length": 44}
{"curie": "MONDO:0005744", "names": ["yolk sac tumor", "yolk Sac tumor", "Orchioblastoma", "Yolk Sac Tumor", "Yolk sac tumor", "orchioblastoma", "Tumor, Yolk Sac", "Yolk sac tumour", "Yolk Sac Tumors", "Tumors, Yolk Sac", "Yolk Sac Neoplasm", "yolk Sac neoplasm", "Yolk Sac neoplasm", "Carcinoma, Yolk Sac", "Endodermal Sinus Tumor", "endodermal sinus tumor", "Endodermal sinus tumor", "ENDODERMAL SINUS TUMOR", "Tumor, Endodermal Sinus", "Hepatoid yolk sac tumor", "Endodermal Sinus Tumors", "Endodermal sinus tumour", "endodermal sinus tumour", "Hepatoid yolk sac tumour", "hepatoid yolk sac tumour", "Tumors, Endodermal Sinus", "Yolk sac tumor (disorder)", "yolk SAC tumor, malignant", "Endodermal Sinus Neoplasm", "Yolk sac tumor, malignant", "endodermal sinus neoplasm", "YOLK SAC TUMOR, MALIGNANT", "yolk sac tumor (diagnosis)", "Infantile embryonal carcinoma", "Polyvesicular vitelline tumor", "infantile embryonal carcinoma", "Embryonal carcinoma, infantile", "Polyvesicular vitelline tumour", "Yolk sac tumor site unspecified", "Yolk Sac Tumor Site Unspecified", "yolk Sac tumor site unspecified", "Yolk sac tumour site unspecified", "yolk Sac tumour site unspecified", "Yolk Sac Tumour Site Unspecified", "Embryonal carcinoma, infantile type", "Endodermal sinus tumor site unspecified", "Endodermal sinus tumour site unspecified", "Endodermal sinus tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "yolk sac tumor", "shortest_name_length": 14}
{"curie": "MONDO:0017764", "names": ["Zinc disorders", "Zinc Disorders", "Zinc metabolism disorder", "metabolic disorder; zinc", "zinc; metabolic disorder", "disorder of zinc metabolism", "Disorder of zinc metabolism", "Disorders of zinc metabolism", "disorders of zinc metabolism", "Disorder of zinc metabolism, NOS", "Disorder of zinc metabolism (disorder)", "disorders of zinc metabolism (diagnosis)", "Disorder of zinc metabolism and transport", "disorder of zinc metabolism and transport"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of zinc metabolism", "shortest_name_length": 14}
{"curie": "MONDO:0013416", "names": ["ARMD8", "age related macular degeneration 8", "MACULAR DEGENERATION, AGE-RELATED, 8", "macular degeneration, age-related, 8", "ARMS2 age-related macular degeneration", "age related macular degeneration type 8", "macular Degeneration, age-related, type 8", "age-related macular degeneration caused by mutation in ARMS2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "age related macular degeneration 8", "shortest_name_length": 5}
{"curie": "MONDO:0000465", "names": ["AVB", "AV Block", "AV BLOCK", "AV block", "av block", "Block, AV", "AV Blocks", "A-V block", "Blocks, AV", "AV block, NOS", "AV block (NOS)", "AV nodal block", "av heart block", "AV BLOCK (NOS)", "HEART BLOCK AV", "Heart block AV", "Atrioventricular Block", "ATRIOVENTRICULAR BLOCK", "atrioventricular block", "Atrioventricular block", "Block;atrioventricular", "Atrioventricular Blocks", "atrioventricular blocks", "block; atrioventricular", "atrioventricular; block", "Atrioventricular block NOS", "Atrioventricular block, NOS", "AVB - Atrioventricular block", "Atrioventricular block (NOS)", "HEART BLOCK ATRIOVENTRICULAR", "ATRIOVENTRICULAR BLOCK (NOS)", "atrioventricular heart block", "Heart block atrioventricular", "Atrioventricular heart block", "Atrioventricular nodal disease", "atrioventricular block (disease)", "Atrioventricular conduction block", "Atrioventricular block (disorder)", "Atrioventricular Conduction Block", "Conduction Block, Atrioventricular", "Unspecified atrioventricular block", "Atrioventricular Conduction Blocks", "atrioventricular block (diagnosis)", "Conduction Blocks, Atrioventricular", "Atrioventricular block, unspecified", "Atrioventricular Block by ECG Finding", "Atrioventricular Block by EKG Finding", "Interruption of electrical communication between upper and lower chambers of heart"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrioventricular block", "shortest_name_length": 3}
{"curie": "MONDO:0024533", "names": ["PHT", "PPH1", "Pph1 With Hht", "PPH1 WITH HHT", "Pph1 with Hht", "pulmonary arterial hypertension", "Primary Pulmonary Hypertension-1", "pulmonary hypertension, primary, 1", "Pulmonary Hypertension, Primary, 1", "PULMONARY HYPERTENSION, PRIMARY, 1", "BMPR2 primary pulmonary hypertension", "familial pulmonary hypertension PPH1", "familial pulmonary hypertension PPH1 (diagnosis)", "Pulmonary Hypertension, Primary, Fenfluramine-Associated", "PULMONARY HYPERTENSION, PRIMARY, FENFLURAMINE-ASSOCIATED", "pulmonary hypertension, primary, Fenfluramine-associated", "primary pulmonary hypertension caused by mutation in BMPR2", "Pulmonary Hypertension, Primary, Dexfenfluramine-Associated", "PULMONARY HYPERTENSION, PRIMARY, DEXFENFLURAMINE-ASSOCIATED", "pulmonary hypertension, primary, Dexfenfluramine-associated", "pulmonary hypertension, familial primary, 1, with or without HHT", "pulmonary hypertension, primary, fenfluramine or dexfenfluramine-associated", "pulmonary hypertension, primary, 1, with hereditary hemorrhagic telangiectasia", "PULMONARY HYPERTENSION, PRIMARY, 1, WITH HEREDITARY HEMORRHAGIC TELANGIECTASIA", "Pulmonary Hypertension, Primary, 1, With Hereditary Hemorrhagic Telangiectasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary hypertension, primary, 1", "shortest_name_length": 3}
{"curie": "MONDO:0020155", "names": ["eyelid border anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eyelid border anomaly", "shortest_name_length": 21}
{"curie": "MONDO:0018319", "names": ["FEPS", "familial episodic pain syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial episodic pain syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0001949", "names": ["Thyroiditis acute", "thyroiditis acute", "THYROIDITIS ACUTE", "Acute Thyroiditis", "acute thyroiditis", "Acute thyroiditis", "thyroiditis; acute", "acute; thyroiditis", "acute thyroiditis (disease)", "Acute thyroiditis (disorder)", "thyroiditis (disease), acute", "acute thyroiditis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute thyroiditis", "shortest_name_length": 17}
{"curie": "MONDO:0000381", "names": ["infiltrating renal pelvis transitional cell carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infiltrating renal pelvis transitional cell carcinoma", "shortest_name_length": 53}
{"curie": "MONDO:0002462", "names": ["Kidney Scarring", "bright's disease", "Scarring, Kidney", "Glomerulonephritis", "GLOMERULONEPHRITIS", "glomerulonephritis", "Glomerulonephritides", "Glomerular nephritis", "Glomerular Nephritis", "glomerulonephritides", "Nephritis-glomerular", "glomerular nephritis", "glomerulonephritis NOS", "Glomerulonephritis NOS", "GN - Glomerulonephritis", "Glomerulonephritis, NOS", "renal glomerulus nephritis", "glomerulonephritis (disease)", "Glomerulonephritis (disorder)", "nephritis of renal glomerulus", "glomerulonephritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glomerulonephritis", "shortest_name_length": 15}
{"curie": "MONDO:0008728", "names": ["CAH1", "21-OHD", "CYP21 DEFICIENCY", "CYP21 Deficiency", "CYP21 deficiency", "classic 21-OHD CAH", "Classic 21-OHD CAH", "adrenal hyperplasia 3", "ADRENAL HYPERPLASIA III", "Adrenal hyperplasia III", "21-Hydroxylase Deficieny", "21-Hydroxylase deficiency", "21-hydroxylase deficiency", "21 hydroxylase deficiency", "21-HYDROXYLASE DEFICIENCY", "21-Hydroxylase Deficiency", "deficiency; 21-hydroxylase", "21-hydroxylase; deficiency", "Adrenal Gland Hyperplasia III", "CAH - 21-hydroxylase deficiency", "21 alpha hydroxylase deficiency", "congenital adrenal hyperplasia 1", "Congenital adrenal hyperplasia 1", "CONGENITAL ADRENAL HYPERPLASIA 1", "Congenital Adrenal Hyperplasia 1", "Steroid 21-hydroxylase deficiency", "Steroid 21-Monooxygenase Deficiency", "Deficiency of steroid 21-hydroxylase", "Simple virilizing adrenal hyperplasia", "Simple virilising adrenal hyperplasia", "Congenital adrenal hyperplasia, type 1", "Deficiency of steroid 21-monooxygenase", "21-hydroxylase deficiency (non salt losing)", "21-hydroxylase deficiency (non-salt losing)", "Simple-virilising congenital adrenal hyperplasia", "Simple-virilizing congenital adrenal hyperplasia", "Deficiency of steroid 21-monooxygenase (disorder)", "Adrenogenital disorder due to 21-hydroxylase deficiency", "21-hydroxylase deficiency (non-salt losing) (diagnosis)", "Steroid 21-hydroxylase deficiency, simple virilizing type", "Steroid 21-hydroxylase deficiency, simple virilising type", "Steroid 21-monooxygenase deficiency, simple virilizing type", "Steroid 21-monooxygenase deficiency, simple virilising type", "congenital adrenal hyperplasia due to 21-hydroxylase deficiency", "Congenital adrenal hyperplasia due to 21 hydroxylase deficiency", "ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY", "adrenal hyperplasia, congenital, due to 21-HYDROXYLASE deficiency", "adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency", "hyperandrogenism, Nonclassic type, due to 21-Hydroxylase deficiency", "Hyperandrogenism, Nonclassic Type, due to 21-Hydroxylase Deficiency", "HYPERANDROGENISM, NONCLASSIC TYPE, DUE TO 21-HYDROXYLASE DEFICIENCY", "Steroid 21-monooxygenase deficiency, simple virilizing type (disorder)", "classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency", "Adrenal Gland Hyperplasia, Congenital, due to 21-Hydroxylase Deficiency", "Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency", "Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0019052", "names": ["rare metabolic disease", "Inborn Metabolism Error", "Metabolism Inborn Error", "inborn error metabolism", "Metabolism Inborn Errors", "Inborn Metabolism Errors", "Inborn Errors Metabolism", "errors inborn metabolism", "Metabolism Error, Inborn", "inborn errors metabolism", "Error, Inborn Metabolism", "Inborn Errors Metabolisms", "Errors Metabolism, Inborn", "Metabolism, Inborn Errors", "Metabolism Errors, Inborn", "Errors, Inborn Metabolism", "inborn metabolic disorder", "inborn error of metabolism", "Inborn Error of Metabolism", "inborn metabolism disorder", "Errors Metabolisms, Inborn", "Inborn error of metabolism", "Metabolisms, Inborn Errors", "inborn errors of metabolism", "Inborn Errors of Metabolism", "Inborn errors of metabolism", "Metabolism, Inborn errors of", "hereditary metabolic disease", "inherited metabolic disorder", "Congenital Metabolic Disorder", "metabolic hereditary disorder", "Metabolic hereditary disorder", "congenital metabolic disorder", "inborn disorders of metabolism", "Congenital Metabolism Disorder", "Inborn error of metabolism NOS", "congenital metabolism disorder", "Inborn error of metabolism, NOS", "rare inborn errors of metabolism", "inherited disorder of metabolism", "IEM - Inborn error of metabolism", "IBEM - Inborn error of metabolism", "inherited disorders of metabolism", "rare inherited metabolic disorder", "Inborn error of metabolism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn errors of metabolism", "shortest_name_length": 22}
{"curie": "UMLS:C0973461", "names": ["Dysphasia", "dysphasia", "DYSPHASIA", "dysphasias", "Dysphasia (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dysphasia", "shortest_name_length": 9}
{"curie": "MONDO:0014836", "names": ["CMT2CC", "NEFH Charcot-Marie-Tooth disease", "Charcot-Marie-Tooth neuropathy type 2CC", "Charcot-Marie-Tooth neuropathy, type 2Cc", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2CC", "Charcot-Marie-Tooth disease axonal type 2CC", "Charcot-Marie-Tooth disease, axonal, type 2cc", "Charcot-Marie-Tooth disease, axonal, type 2CC", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2CC", "Charcot-Marie-Tooth disease caused by mutation in NEFH"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease axonal type 2CC", "shortest_name_length": 6}
{"curie": "UMLS:C1514519", "names": ["Prostatic Duct Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostatic Duct Urothelial Carcinoma", "shortest_name_length": 35}
{"curie": "MONDO:0005973", "names": ["Strongylida Infection", "Infection, Strongylida", "Strongylida Infections", "Infections, Strongylida", "Strongylida infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Strongylida infectious disease", "shortest_name_length": 21}
{"curie": "MONDO:0012992", "names": ["pancreatic insufficiency-anemia-hyperostosis syndrome", "pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome", "Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome", "Pancreatic insufficiency, dyserythropoietic anaemia, calvarial hyperostosis syndrome", "exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis", "Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis", "EXOCRINE PANCREATIC INSUFFICIENCY, DYSERYTHROPOIETIC ANEMIA, AND CALVARIAL HYPEROSTOSIS", "Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic insufficiency-anemia-hyperostosis syndrome", "shortest_name_length": 53}
{"curie": "MONDO:0044791", "names": ["cHCC-CC", "cHCC-CCA", "Combined HCC-CC", "Cholangiohepatoma", "CHOLANGIOHEPATOMA", "cholangiohepatoma", "Hepatocholangiocarcinoma", "HEPATOCHOLANGIOCARCINOMA", "hepatocholangiocarcinoma", "Carcinoma of liver and IBT", "Mixed Hepatocellular Cholangiocarcinoma", "Mixed hepatocellular cholangiocarcinoma", "Combined hepatocellular-cholangiocarcinoma", "HEPATOCELLULAR, CHOLANGIOCARCINOMA COMBINED", "Mixed hepatocellular and bile duct carcinoma", "hepatocellular carcinoma; cholangiocarcinoma", "Liver and Intrahepatic Biliary Tract Carcinoma", "Combined hepatocellular and cholangiocarcinoma", "liver and intrahepatic biliary tract carcinoma", "hepatocellular carcinoma and cholangiocarcinoma", "Carcinoma of liver and intrahepatic biliary tract", "carcinoma of liver and intrahepatic biliary tract", "Carcinoma of Liver and Intrahepatic Biliary Tract", "cholangiocarcinoma; with hepatocellular carcinoma", "carcinoma of the liver and intrahepatic biliary tract", "Carcinoma of the Liver and Intrahepatic Biliary Tract", "adult primary mixed hepatocellular cholangiocarcinoma", "combined hepatocellular carcinoma and cholangiocarcinoma", "Combined hepatocellular carcinoma and cholangiocarcinoma", "Combined Hepatocellular Carcinoma and Cholangiocarcinoma", "hepatocellular carcinoma and cholangiocarcinoma (diagnosis)", "liver neoplasm hepatocellular carcinoma & cholangiocarcinoma", "Combined hepatocellular carcinoma and cholangiocarcinoma (disorder)", "combined hepatocellular cancer and cholangiocarcinoma (bile duct cancer)", "Combined hepatocellular carcinoma and cholangiocarcinoma (morphologic abnormality)", "combined hepatocellular cancer and intrahepatic bile duct cancer (cholangiocarcinoma)", "Combined Hepatocellular Cancer and Intrahepatic Bile Duct Cancer (Cholangiocarcinoma)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined hepatocellular carcinoma and cholangiocarcinoma", "shortest_name_length": 7}
{"curie": "UMLS:C1321132", "names": ["Spontaneous hemorrhage", "Spontaneous haemorrhage", "Spontaneous hemorrhage, NOS", "Spontaneous haemorrhage, NOS", "Spontaneous hemorrhage (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spontaneous hemorrhage", "shortest_name_length": 22}
{"curie": "MONDO:0021913", "names": ["Aquagenic pruritus", "aquagenic pruritus", "Water-induced itching", "water-induced itching", "Aquagenic pruritus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aquagenic pruritus", "shortest_name_length": 18}
{"curie": "MONDO:0009136", "names": ["DKCB", "DKCB1", "dyskeratosis congenita autosomal recessive", "autosomal recessive dyskeratosis congenita", "Autosomal recessive dyskeratosis congenita", "Dyskeratosis Congenita, Autosomal Recessive", "autosomal recessive dyskeratosis congenita 1", "dyskeratosis congenita, autosomal recessive 1", "DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 1", "Dyskeratosis Congenita, Autosomal Recessive 1", "dyskeratosis congenita, autosomal recessive type 1", "Autosomal recessive dyskeratosis congenita (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyskeratosis congenita, autosomal recessive 1", "shortest_name_length": 4}
{"curie": "MONDO:0030896", "names": ["chromosome 13q33-q34 deletion syndrome", "CHROMOSOME 13q33-q34 DELETION SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 13q33-q34 deletion syndrome", "shortest_name_length": 38}
{"curie": "MONDO:0013826", "names": ["DFNB86", "autosomal recessive deafness 86", "DEAFNESS, AUTOSOMAL RECESSIVE 86", "deafness, autosomal recessive 86", "deafness, autosomal recessive type 86", "autosomal recessive nonsyndromic deafness 86", "autosomal recessive nonsyndromic hearing loss 86", "TBC1D24 autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic deafness type 86", "autosomal recessive nonsyndromic deafness caused by mutation in TBC1D24"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 86", "shortest_name_length": 6}
{"curie": "MONDO:0017824", "names": ["FIPA", "familial isolated pituitary adenoma", "Familial isolated pituitary adenoma", "Pituitary Adenoma, Familial Isolated", "PITUITARY ADENOMA, FAMILIAL ISOLATED", "Familial isolated pituitary adenoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial isolated pituitary adenoma", "shortest_name_length": 4}
{"curie": "MONDO:0027668", "names": ["flucloxacilline toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "flucloxacilline toxicity", "shortest_name_length": 24}
{"curie": "MONDO:0009215", "names": ["FA", "FANCA", "FANCONI ANEMIA", "Fanconi Anemia", "FANCA Fanconi anemia", "Fanconi anemia complementation group A", "Fanconi Anemia, Estren-Dameshek variant", "Fanconi Anemia, Estren-Dameshek Variant", "FANCONI ANEMIA, COMPLEMENTATION GROUP A", "Fanconi Anemia, Complementation Group A", "FANCONI ANEMIA, ESTREN-DAMESHEK VARIANT", "Fanconi anemia, complementation group A", "ESTREN-DAMESHEK VARIANT OF FANCONI ANEMIA", "Estren-Dameshek variant of Fanconi Anemia", "Estren-Dameshek Variant of Fanconi Anemia", "Fanconi anemia caused by mutation in FANCA", "Fanconi anemia complementation group type A", "Fanconi Anemia, complementation group type a", "ESTREN-DAMESHEK VARIANT OF FANCONI PANCYTOPENIA", "Estren-Dameshek Variant of Fanconi Pancytopenia", "Estren-Dameshek variant of Fanconi pancytopenia", "Fanconi anemia complementation group A (diagnosis)", "FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fanconi anemia complementation group A", "shortest_name_length": 2}
{"curie": "UMLS:C0853812", "names": ["Visceral Artery Ischemia", "Mesenteric Artery Ischemia", "Visceral arterial ischemia", "Visceral arterial ischaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Visceral Artery Ischemia", "shortest_name_length": 24}
{"curie": "MONDO:0008963", "names": ["CHS", "Chediak-Higashi", "Chédiak anomaly", "Chediak anomaly", "Steinbrinck anomaly", "Begnez Cesar disease", "Beguez Cesar disease", "Béguez César disease", "BEGUEZ CESAR DISEASE", "Chediak-Higashi anomaly", "chediak higashi anomaly", "Chediak-Higashi disease", "Chediak Higashi anomaly", "Chédiak-Higashi disease", "Chediak-Higashi; anomaly", "Chediak Higashi syndrome", "CHEDIAK-HIGASHI SYNDROME", "chediak-higashi syndrome", "Chediak Higashi Syndrome", "chediak higashi syndrome", "Chediak-Higashi syndrome", "Chediak-Higashi Syndrome", "ChC)diak-Higashi disease", "Chédiak-Higashi syndrome", "anomaly; Chediak-Higashi", "hereditary leukomelanopathy", "Hereditary leukomelanopathy", "Chediak-Steinbrinck anomaly", "Chédiak-Steinbrinck anomaly", "leukomelanopathy; hereditary", "Leukocyte granulation anomaly", "Chediak - Steinbrinck anomaly", "Granulation anomaly of leucocytes", "Granulation anomaly of leukocytes", "Chédiak-Higashi-Steinbrink syndrome", "Chédiak-Higashi syndrome (disorder)", "Chediak-Higashi disease (diagnosis)", "Chediak-Steinbrinck-Higashi syndrome", "ChC)diak-Higashi-Steinbrink syndrome", "Chediak-Steinbrinck-Higashi Syndrome", "Chediak Steinbrinck Higashi Syndrome", "Chediak-Steinbrinck-Higashi Syndromes", "hereditary leukomelanopathy (diagnosis)", "Anomaly or syndrome, Chediak-Steinbrinck", "Congenital gigantism of peroxidase granules", "Oculocutaneous albinism with leukocyte defect", "Oculocutaneous Albinism with Leukocyte Defect", "Hereditary gigantism of cytoplasmic organelles", "Anomaly or syndrome, Chediak-Steinbrinck-Higashi", "Granulocyte anomaly or syndrome, Chediak-Steinbrinck", "Granulation anomaly or syndrome, Chediak-Steinbrinck", "Granulocyte anomaly or syndrome, Chediak-Steinbrinck-Higashi", "Granulation anomaly or syndrome, Chediak-Steinbrinck-Higashi"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chediak-Higashi syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0030294", "names": ["MMIHS3", "megacystis-microcolon-intestinal hypoperistalsis syndrome 3", "MEGACYSTIS-MICROCOLON-INTESTINAL HYPOPERISTALSIS SYNDROME 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "megacystis-microcolon-intestinal hypoperistalsis syndrome 3", "shortest_name_length": 6}
{"curie": "UMLS:C4331322", "names": ["Stage II Lip and Oral Cavity Cancer", "Stage II Lip and Oral Cavity Cancer AJCC v8", "Stage II Lip and Oral Cavity Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Lip and Oral Cavity Cancer AJCC v8", "shortest_name_length": 35}
{"curie": "MONDO:0024356", "names": ["Primary central sleep apnea", "Primary Central Sleep Apnea", "primary central sleep apnea", "Primary central sleep apnoea", "Central Sleep Apnea, Primary", "organic primary central sleep apnea", "primary central sleep apnea syndrome", "Primary central sleep apnea (disorder)", "primary central sleep apnea (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary central sleep apnea syndrome", "shortest_name_length": 27}
{"curie": "MONDO:0018500", "names": ["CLM", "Dew Itch", "sandworm", "Sandworm", "dew itch", "Itch, Dew", "Dew Itchs", "Itchs, Dew", "Ground Itch", "Ground itch", "ground itch", "coolie; itch", "itch; coolie", "ground; itch", "Itch, Ground", "Ground Itchs", "itch; ground", "Itchs, Ground", "Larva migrans", "larva migrans", "Larva Migrans", "Plumber's itch", "eruption creeping", "Creeping Eruption", "Creeping eruption", "creeping eruption", "Duckhunter's itch", "creeping; eruption", "eruption; creeping", "Eruption, Creeping", "creeping eruptions", "Creeping Eruptions", "Eruptions, Creeping", "Uncinarial dermatitis", "Larva migrans of skin", "Creeping eruption NOS", "cutaneous larva migran", "larva migrans cutaneous", "cutaneous larva migrans", "Cutaneous Larva Migrans", "Cutaneous larva migrans", "cutaneous; larva migrans", "larva migrans; cutaneous", "Cutaneous larval migrans", "Larva Migrans, Cutaneous", "Hookworm cutaneous vesicle", "Cutaneous larva migrans NOS", "eruption; creeping eruption", "creeping eruption; eruption", "CLM - Cutaneous larva migrans", "Cutaneous larva migrans (disorder)", "cutaneous larva migrans (diagnosis)", "skin; eruption, creeping eruption (meaning hookworm)", "eruption; skin, creeping eruption (meaning hookworm)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous larva migrans", "shortest_name_length": 3}
{"curie": "MONDO:0700143", "names": ["canine mammary carcinoma", "Canine Mammary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canine mammary carcinoma", "shortest_name_length": 24}
{"curie": "UMLS:C0920028", "names": ["Leukemia relapse", "leukemia relapse", "relapse leukemia", "leukemia relapses", "Leukaemia relapse", "Leukemia recurrent", "Recurrent Leukemia", "leukemia in relapse", "Leukaemia recurrent", "leukemia in relapse (diagnosis)", "Unspecified leukemia, in relapse", "Leukemia, unspecified, in relapse"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leukemia recurrent", "shortest_name_length": 16}
{"curie": "MONDO:0005654", "names": ["ASCARIASIS", "ascariasis", "ascariosis", "Ascariosis", "Ascariases", "Ascariasis", "ascaridiasis", "Ascaris Infection", "Ascaris; infection", "Ascaris Infections", "Infection, Ascaris", "Infections, Ascaris", "Ascariasis (disorder)", "ascariasis - roundworm", "Ascariasis - roundworm", "ascariasis (diagnosis)", "Ascariasis, unspecified", "Ascariasis - roundworms", "Ascaris lumbricoides infection", "infestation; Ascaris lumbricoides", "Ascaris lumbricoides; infestation", "Ascaris lumbricoides infectious disease", "Ascaris lumbricoides disease or disorder", "Ascaris lumbricoides caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ascariasis", "shortest_name_length": 10}
{"curie": "MONDO:0017745", "names": ["disorder of O-mannosylglycan synthesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of O-mannosylglycan synthesis", "shortest_name_length": 38}
{"curie": "MONDO:0006014", "names": ["Candidal cervix", "candidal: cervix", "vaginal candidiasis", "Vaginal Candidiasis", "Vulvovaginal thrush", "Vulvovaginal candida", "THRUSH, VULVOVAGINAL", "VULVOVAGINITIS CANDIDA", "candida vulvovaginitis", "candidal vulvovaginitis", "moniliasis vulvovaginal", "Vulvovaginal Moniliasis", "monilial vulvovaginitis", "Monilial vulvovaginitis", "Candidal vulvovaginitis", "VULVOVAGINITIS, MYCOTIC", "Moniliasis, Vulvovaginal", "candidiasis vagina vulva", "Vulvovaginal candidiasis", "Vulvovaginal Candidiasis", "VULVOVAGINAL CANDIDIASIS", "candidiasis vulvovaginal", "vulvovaginal candidiasis", "Candidiasis, Vulvovaginal", "Candidiasis, vulvovaginal", "candidiasis of vulva and vagina", "Candidiasis of vulva and vagina", "Candida albicans vulvovaginitis", "Candidal vulvovaginitis (disorder)", "Candidiasis of vulva and vagina NOS", "candidal vulvovaginitis (diagnosis)", "candidal: [vulvovaginitis NOS] or [cervix]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvovaginal candidiasis", "shortest_name_length": 15}
{"curie": "UMLS:C4553872", "names": ["stage 0is urethral cancer", "Stage 0is Urethral Cancer", "stage 0is urethral cancer AJCC v8", "Stage 0is Urethral Cancer AJCC v8", "stage 0is urethral carcinoma AJCC v8", "Stage 0is Urethral Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0is Urethral Cancer AJCC v8", "shortest_name_length": 25}
{"curie": "MONDO:0010781", "names": ["adult-onset ataxia and polyneuropathy", "ataxia and polyneuropathy, adult-onset", "ATAXIA AND POLYNEUROPATHY, ADULT-ONSET", "Ataxia and Polyneuropathy, Adult-Onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ataxia and polyneuropathy, adult-onset", "shortest_name_length": 37}
{"curie": "MONDO:0012774", "names": ["Del(15)(q13.3)", "monosomy 15q13.3", "Monosomy 15q13.3", "15q13.3 Microdeletion", "15q13.3 microdeletion", "15q13.3 deletion syndrome", "microdeletion 15q13.3 syndrome", "15q13.3 microdeletion syndrome", "Microdeletion 15q13.3 Syndrome", "15q13.3 Microdeletion Syndrome", "Microdeletion of chromosome 15q13.3", "CHROMOSOME 15q13.3 DELETION SYNDROME", "Chromosome 15q13.3 Deletion Syndrome", "chromosome 15q13.3 deletion syndrome", "chromosome 15q13.3 microdeletion syndrome", "CHROMOSOME 15q13.3 MICRODELETION SYNDROME", "Chromosome 15q13.3 Microdeletion Syndrome", "Microdeletion of chromosome 15q13.3 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 15q13.3 microdeletion syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C1707543", "names": ["Skin Fibrous Histiocytoma, Cellular Variant", "Cutaneous Fibrous Histiocytoma, Cellular Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin Fibrous Histiocytoma, Cellular Variant", "shortest_name_length": 43}
{"curie": "MONDO:0010722", "names": ["PRD", "X-linked retinal dysplasia", "RETINAL DYSPLASIA, PRIMARY", "retinal dysplasia X-linked", "retinal dysplasia, primary", "X-linked retinal dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked retinal dysplasia", "shortest_name_length": 3}
{"curie": "MONDO:0000107", "names": ["Cosman ear", "Question mark ear", "question mark ear", "dysgnathia complex", "Dysgnathia complex", "Auriculocondylar syndrome", "auriculocondylar syndrome", "Auriculo-condylar syndrome", "question mark ear syndrome", "question-mark ear syndrome", "Question-mark ear syndrome", "auriculo-condylar syndrome", "Question mark ear syndrome", "Question-Mark Ear Syndrome", "Question Mark Ears Syndrome", "QUESTION MARK EARS SYNDROME", "Ears prominent and constricted", "ears prominent and constricted", "Auriculo-condylar syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "auriculocondylar syndrome", "shortest_name_length": 10}
{"curie": "MONDO:0002948", "names": ["Pinkus Tumor", "pinkus tumor", "Pinkus tumor", "Pinkus tumour", "pinkus tumour", "Fibroepithelioma", "fibroepithelioma", "fibroepithelioma pinkus", "fibroepithelioma of pinkus", "fibroepithelioma of Pinkus", "Fibroepithelioma of pinkus", "Fibroepithelioma of Pinkus", "fibroepithelioma of Pinkus type", "Fibroepithelioma of Pinkus type", "Fibroepithelial Basal Cell Carcinoma", "Fibroepithelial basal cell carcinoma", "fibroepithelial basal cell carcinoma", "Fibroepithelioma of Pinkus (disorder)", "Basal cell carcinoma, fibroepithelial", "Fibroepithelioma of Pinkus (diagnosis)", "skin fibroepithelial basal cell carcinoma", "Skin Fibroepithelial Basal Cell Carcinoma", "Basal cell carcinoma, fibroepithelial type", "Fibroepithelial basal cell carcinoma, Pinkus type", "Basal cell carcinoma, fibroepithelial (morphologic abnormality)", "skin neoplasm malignant carcinoma basal cell fibroepithelioma of pinkus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin fibroepithelial basal cell carcinoma", "shortest_name_length": 12}
{"curie": "UMLS:C4524969", "names": ["stage IV small intestine cancer", "Stage IV Small Intestinal Adenocarcinoma", "Stage IV Small Intestinal Adenocarcinoma AJCC v8", "stage IV small intestinal adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Small Intestinal Adenocarcinoma AJCC v8", "shortest_name_length": 31}
{"curie": "MONDO:0003757", "names": ["PARAPLEGIA", "Paraplegia", "paraplegia", "Paraplegias", "leg paralysis", "Leg paralysis", "Paralysis leg", "leg; paralysis", "Paralysis legs", "paralysis; leg", "Paralysis, Legs", "paralysis of leg", "Lower paraplegia", "Paraplegia, lower", "paraplegia, lower", "Hindlimb paralysis", "paralysis; leg, both", "leg; paralysis, both", "Paraplegia (disorder)", "Paralysis, Lower Limbs", "paralysis in both legs", "Paraplegia (lower) NOS", "Paraplegia, unspecified", "paralysis of leg (symptom)", "EXTREMITY PARALYSIS, LOWER", "extremities lower paralysis", "Paralysis, Lower Extremities", "Paralysis of both lower limbs", "paralysis was seen in both legs", "Paralysis of both lower limbs NOS", "paralysis in both legs (physical finding)", "Paraplegia (complete or partial paralysis of legs)", "severe or complete loss of motor function in the lower extremities and lower portions of the trunk"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paraplegia", "shortest_name_length": 10}
{"curie": "UMLS:C1707744", "names": ["Diffuse Pulmonary Lymphangiomatosis", "Diffuse pulmonary lymphangiomatosis", "Diffuse pulmonary lymphangiomatosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse pulmonary lymphangiomatosis", "shortest_name_length": 35}
{"curie": "MONDO:0032717", "names": ["AI3C", "amelogenesis imperfecta type 3C", "amelogenesis imperfecta, type 3c", "amelogenesis imperfecta type IIIC", "AMELOGENESIS IMPERFECTA, TYPE IIIC", "autosomal recessive amelogenesis imperfecta hypocalcification type", "Amelogenesis Imperfecta, Hypocalcification Type, Autosomal Recessive", "AMELOGENESIS IMPERFECTA, HYPOCALCIFICATION TYPE, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amelogenesis imperfecta, type 3c", "shortest_name_length": 4}
{"curie": "MONDO:0006937", "names": ["pulpitis", "Pulpitis", "Pulpitides", "pulp stones", "Pulpitis, NOS", "Pulpitis dental", "dental pulpitis", "Pulpitis (disorder)", "pulpitis (diagnosis)", "Endodontic Inflammation", "Inflammation, Endodontic", "Endodontic Inflammations", "dental pulp inflammation", "Inflammations, Endodontic", "Inflammation of tooth pulp", "inflammation of dental pulp"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulpitis", "shortest_name_length": 8}
{"curie": "UMLS:C5238495", "names": ["Adnexal Cribriform Carcinoma", "Adnexal Solid-Cribriform Carcinoma", "Primary Cutaneous Cribriform Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adnexal Cribriform Carcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0011999", "names": ["OTSC3", "OTOSCLEROSIS 3", "Otosclerosis 3", "otosclerosis 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "otosclerosis 3", "shortest_name_length": 5}
{"curie": "MONDO:0012703", "names": ["LIS3", "LISSENCEPHALY 3", "lissencephaly 3", "Lissencephaly 3", "Type 3 lissencephaly", "Lissencephaly type 3", "Type III lissencephaly", "Lissencephaly type III", "Type 3 lissencephaly (disorder)", "lissencephaly due to TUBA1A mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lissencephaly due to TUBA1A mutation", "shortest_name_length": 4}
{"curie": "UMLS:C1301518", "names": ["Vaccinia keratitis", "vaccinia keratitis", "Vaccinia keratitis (disorder)", "vaccinia keratitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaccinia keratitis", "shortest_name_length": 18}
{"curie": "MONDO:0016603", "names": ["CTLN2", "Citrin deficiency", "CITRIN DEFICIENCY", "Citrullinemia type 2", "citrullinemia type 2", "Citrullinemia type II", "citrullinemia type II", "Citrullinemia Type II", "Citrullinaemia type II", "Citrullinemia, type II", "Adult onset citrin deficiency", "Adult-onset citrin deficiency", "adult-onset citrin deficiency", "Adult onset type 2 citrullinemia", "Adult-onset citrullinemia type 2", "Citrullinemia type II (disorder)", "adult-onset type 2 citrullinemia", "Adult onset type 2 citrullinaemia", "adult-onset type II citrullinemia", "Adult-onset citrullinemia type II", "CITRULLINEMIA, TYPE II, ADULT-ONSET", "Citrullinemia, Type II, Adult-Onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "citrullinemia type II", "shortest_name_length": 5}
{"curie": "MONDO:0007252", "names": ["DA3", "Gordon syndrome", "GORDON SYNDROME", "Gordon's syndrome", "arthrogryposis distal type 3", "distal arthrogryposis type 3", "Distal arthrogryposis type 3", "Distal arthrogryposis, type 3", "Distal arthrogryposis type IIA", "Arthrogryposis, distal, type 3", "arthrogryposis, distal, type 3", "ARTHROGRYPOSIS, DISTAL, TYPE 3", "distal arthrogryposis type IIA", "Distal arthrogryposis type 3 (disorder)", "arthrogryposis distal type 3 (diagnosis)", "Camptodactyly, cleft palate, and clubfoot", "CAMPTODACTYLY, CLEFT PALATE, AND CLUBFOOT", "camptodactyly, cleft palate, and clubfoot", "camptodactyly-cleft palate-clubfoot syndrome", "Camptodactyly-cleft palate-clubfoot syndrome", "distal arthrogryposis multiplex congenita type IIA", "arthrogryposis multiplex congenita, distal, type 2A", "Arthrogryposis multiplex congenita, distal, type 2a", "ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE IIA", "Arthrogryposis Multiplex Congenita, Distal, Type IIa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gordon syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0018913", "names": ["MG body", "malakoplakia", "Malakaplakia", "Malakoplakia", "Malacoplakia", "malacoplakia", "Malacoplakias", "Malakoplakias", "Malakoplakia, NOS", "Malacoplakia, NOS", "Michaelis-Gutmann Body", "Michaelis-Gutmann body", "Malakoplakia (disorder)", "Michaelis-Gutmann bodies", "Malakoplakia (qualifier value)", "Malakoplakia (morphologic abnormality)", "Michaelis-Gutmann body (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malakoplakia", "shortest_name_length": 7}
{"curie": "MONDO:0009614", "names": ["Methylmalonic aciduria cblB type", "Methylmalonic acidemia cblB type", "methylmalonic aciduria cblB type", "methylmalonic acidemia cblB type", "METHYLMALONIC ACIDURIA, cblB TYPE", "Methylmalonic Aciduria, cblB Type", "Methylmalonic Acidemia, cblB Type", "methylmalonic acidemia, cblB type", "METHYLMALONIC ACIDEMIA, cblB TYPE", "methylmalonic aciduria, cblB type", "vitamin B12-responsive methylmalonic acidemia type cblB", "Vitamin B12-responsive methylmalonic acidemia type cblB", "Vitamin B12-responsive methylmalonic aciduria, type cblB", "vitamin B12-responsive methylmalonic aciduria, type cblB", "methylmalonic aciduria, vitamin B12-responsive, cblB type", "METHYLMALONIC ACIDURIA, VITAMIN B12-RESPONSIVE, DUE TO DEFECT IN SYNTHESIS OF ADENOSYLCOBALAMIN, cblB TYPE", "methylmalonic aciduria, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin, cblB type", "methylmalonic aciduria, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin, cblB complementation type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "methylmalonic aciduria, cblB type", "shortest_name_length": 32}
{"curie": "MONDO:0002975", "names": ["breast melanoma", "Breast Melanoma", "breast; melanoma", "melanoma; breast", "Malignant Breast Melanoma", "breast melanoma (disease)", "malignant breast melanoma", "Malignant Melanoma of Breast", "melanoma (disease) of breast", "Malignant melanoma of breast", "malignant melanoma of breast", "malignant melanoma of the breast", "Malignant Melanoma of the Breast", "Malignant melanoma of breast (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant breast melanoma", "shortest_name_length": 15}
{"curie": "MONDO:0006167", "names": ["Combined Lung Cancer", "combined lung cancer", "Combined Lung Carcinoma", "combined lung carcinoma", "Combined Carcinoma of Lung", "combined carcinoma of lung", "combined carcinoma of the lung", "Combined Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined lung carcinoma", "shortest_name_length": 20}
{"curie": "UMLS:C0343402", "names": ["Friedländer; B", "Friedlander bacillus infection", "infection; Bacillus Friedländer", "Friedlander's bacillus infection", "Friedlander's bacillus infection (disorder)", "Bacterial infection due to Klebsiella pneumoniae", "Bacterial infection due to Friedlander's bacillus", "Bacterial infection due to Klebsiella pneumoniae (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bacterial infection due to Klebsiella pneumoniae", "shortest_name_length": 14}
{"curie": "MONDO:0005169", "names": ["mature T-cell neoplasm", "Mature T-Cell Neoplasm", "mature T and NK neoplasms", "Mature T-cell and NK-cell cancer", "mature T-cell and NK-cell neoplasm", "Mature T-Cell and NK-Cell Neoplasm", "mature T-cell and NK-cell neoplasms", "neoplasm of mature T-cells or NK-cells"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplasm of mature T-cells or NK-cells", "shortest_name_length": 22}
{"curie": "MONDO:0007766", "names": ["MSM syndrome", "HYPEROSTOSIS FRONTALIS INTERNA", "hyperostosis frontalis interna", "Hyperostosis frontalis interna", "Hyperostosis interna frontalis", "Hyperostosis Frontalis Interna", "interna frontalis; hyperostosis", "Stewart-Morel-Morgagni syndrome", "hyperostosis; interna frontalis", "Morgagni-Stewart-Morel syndrome", "MORGAGNI-STEWART-MOREL SYNDROME", "Thick inner surface of the frontal bone", "Hyperostosis interna frontalis (finding)", "hyperostosis frontalis interna (diagnosis)", "Thick internal surface of the frontal bone", "Overgrowth of the inside of the frontal bone", "Hyperostosis frontalis, virilism, obesity syndrome", "Overgrowth of the inner surface of the frontal bone", "Enlargement of the inner surface of the frontal bone", "Excessive growth of inner surface of the frontal bone", "Hypertrophy of the internal surface of the frontal bone", "Hyperostosis of the internal surface of the frontal bone", "Increased ossification of the internal surface of the frontal bone", "hyperostosis frontalis interna, obesity, shortness and cognitive impairment"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Morgagni-Stewart-Morel syndrome", "shortest_name_length": 12}
{"curie": "UMLS:C1335468", "names": ["polyp precancerous", "Precancerous Polyp", "precancerous polyps"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Precancerous Polyp", "shortest_name_length": 18}
{"curie": "UMLS:C4553248", "names": ["Stage II", "Stage II Uterine Corpus Cancer AJCC v8", "Stage II Uterine (including Endometrial) Cancer", "Stage II Uterine Corpus Carcinoma or Carcinosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Uterine Corpus Cancer AJCC v8", "shortest_name_length": 8}
{"curie": "MONDO:0029137", "names": ["DFNA74", "deafness, autosomal dominant 74", "DEAFNESS, AUTOSOMAL DOMINANT 74", "hearing loss, autosomal dominant 74", "autosomal dominant nonsyndromic deafness 74"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal dominant 74", "shortest_name_length": 6}
{"curie": "MONDO:0013601", "names": ["GPXD", "GLUTATHIONE PEROXIDASE DEFICIENCY", "glutathione peroxidase deficiency", "gluthathione peroxidase deficiency", "Gluthathione peroxidase deficiency", "Gluthathione peroxidase deficiency (disorder)", "gluthathione peroxidase deficiency (diagnosis)", "hemolytic anemia due to glutathione peroxidase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gluthathione peroxidase deficiency", "shortest_name_length": 4}
{"curie": "UMLS:C4331399", "names": ["Temporal Lobe Ependymal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Temporal Lobe Ependymal Tumor", "shortest_name_length": 29}
{"curie": "UMLS:C1335007", "names": ["Non-Neoplastic Endocrine Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Endocrine Disorder", "shortest_name_length": 33}
{"curie": "UMLS:C0269806", "names": ["INDUCTION FAILED", "failed induction", "Failed induction", "failing induction", "failure; induction", "Failed induction NOS", "failed induction of labor", "Failed induction of labor", "Failed induction of labour", "Unsuccessfully induced labor", "Labor, unsuccessfully induced", "Unsuccessfully induced labour", "Failed induction of labor, NOS", "Failed induction of labour, NOS", "Unsuccessful attempt to induce labor", "Failed induction of labor (disorder)", "failed induction of labor (diagnosis)", "Unsuccessful attempt to induce labour", "Failed induction of labor, unspecified", "Failed induction of labour, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Failed induction of labor", "shortest_name_length": 16}
{"curie": "UMLS:C1504465", "names": ["Device malfunction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Device malfunction", "shortest_name_length": 18}
{"curie": "UMLS:C1735647", "names": ["Mixed liver injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mixed liver injury", "shortest_name_length": 18}
{"curie": "UMLS:C3897124", "names": ["BCLC Stage A Hepatocellular Cancer", "BCLC Stage A Hepatocellular Carcinoma", "Barcelona Clinic Liver Cancer Stage A Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "BCLC Stage A Hepatocellular Carcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0700007", "names": ["idiopathic disease", "idiopathic disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic disease", "shortest_name_length": 18}
{"curie": "UMLS:C0281701", "names": ["Stage I Large Cell Lymphoma", "Pediatric Large Cell Lymphoma Stage I", "Stage I Childhood Large Cell Lymphoma", "Stage I Pediatric Large Cell Lymphoma", "stage I childhood large cell lymphoma", "Childhood Large Cell Lymphoma Stage I", "pediatric large cell lymphoma, stage I", "stage I large cell lymphoma, childhood", "childhood large cell lymphoma, stage I", "lymphoma, stage I childhood large cell", "large cell lymphoma, childhood, stage I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Childhood Large Cell Lymphoma", "shortest_name_length": 27}
{"curie": "MONDO:0004172", "names": ["uterine corpus adenocarcinofibroma", "body of uterus adenocarcinofibroma", "adenocarcinofibroma of body of uterus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine corpus adenocarcinofibroma", "shortest_name_length": 34}
{"curie": "MONDO:0018835", "names": ["Liver regeneration", "liver regeneration", "regeneration liver", "Noncirrhotic nodulation", "non-cirrhotic nodulation", "Non-cirrhotic nodulation", "Liver regeneration disorder", "Liver regeneration (disorder)", "Nodular transformation of liver", "nodular regenerative hyperplasia", "non-cirrhotic portal hypertension", "miliary hepatocellular adenomatosis", "non-cirrhotic nodular transformation", "Partial nodular transformation of liver", "Nodular regenerative hyperplasia of liver", "Nodular regenerative hyperplasia of the liver", "nodular regenerative hyperplasia of the liver", "Partial nodular transformation of liver (disorder)", "Nodular regenerative hyperplasia of liver (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nodular regenerative hyperplasia of the liver", "shortest_name_length": 18}
{"curie": "UMLS:C4527178", "names": ["Stage IA", "Stage IA Cutaneous (Skin) Melanoma", "Pathologic Stage IA Cutaneous Melanoma AJCC v8", "Pathologic Stage IA Melanoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IA Cutaneous Melanoma AJCC v8", "shortest_name_length": 8}
{"curie": "MONDO:0032702", "names": ["CSS8", "COFFIN-SIRIS SYNDROME 8", "Coffin-Siris syndrome 8", "SMARCC2-related BAFopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Coffin-Siris syndrome 8", "shortest_name_length": 4}
{"curie": "MONDO:0030933", "names": ["JBTS37", "JOUBERT SYNDROME 37", "Joubert syndrome 37"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome 37", "shortest_name_length": 6}
{"curie": "MONDO:0024317", "names": ["chronic pain disease", "chronic pain syndrome", "Chronic pain syndrome", "PAIN CHRONIC SYNDROME", "chronic pain syndromes", "chronic disorder involving pain", "Chronic pain syndrome (disorder)", "disorder involving pain, chronic", "chronic pain syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic pain syndrome", "shortest_name_length": 20}
{"curie": "UMLS:C5237324", "names": ["Metastatic Proximal Gastric Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Proximal Gastric Adenocarcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0006386", "names": ["Primary Peritoneal Serous Adenocarcinoma", "primary peritoneal serous adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary peritoneal serous adenocarcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0030260", "names": ["PCH1E", "pontocerebellar hypoplasia type 1E", "pontocerebellar hypoplasia, type 1E", "PONTOCEREBELLAR HYPOPLASIA, TYPE 1E"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pontocerebellar hypoplasia, type 1E", "shortest_name_length": 5}
{"curie": "MONDO:0022810", "names": ["Combarros Calleja Leno syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Combarros Calleja Leno syndrome", "shortest_name_length": 31}
{"curie": "MONDO:0027664", "names": ["cisplatin toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cisplatin toxicity", "shortest_name_length": 18}
{"curie": "UMLS:C5669744", "names": ["Astrocytoma, IDH-Wildtype"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Astrocytoma, IDH-Wildtype", "shortest_name_length": 25}
{"curie": "UMLS:C5238469", "names": ["Locally Advanced Neuroendocrine Tumor", "Locally Advanced Well Differentiated Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Neuroendocrine Tumor", "shortest_name_length": 37}
{"curie": "MONDO:0008174", "names": ["PC2", "PACHYONYCHIA CONGENITA 2", "pachyonychia congenita 2", "KRT17 pachyonychia congenita", "pachyonychia congenita type 2", "Type 2 Pachyonychia Congenita", "Jackson-Lawler Syndrome (Pc-2)", "Pachyonychia Congenita, Type 2", "Jackson Lawler Syndrome (Pc 2)", "Syndrome, Jackson-Lawler (Pc-2)", "Pachyonychia Congenita, Type 2 (disorder)", "Jackson-Lawler Type Pachyonychia Congenita", "Pachyonychia Congenita Jackson Lawler Type", "Jackson Lawler Type Pachyonychia Congenita", "Pachyonychia Congenita, Jackson Lawler Type", "pachyonychia congenita, Jackson-Lawler type", "Pachyonychia Congenita, Jackson-Lawler Type", "pachyonychia congenita caused by mutation in KRT17", "pachyonychia congenita, Jackson-Lawler type, formerly", "PACHYONYCHIA CONGENITA, JACKSON-LAWLER TYPE, FORMERLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pachyonychia congenita 2", "shortest_name_length": 3}
{"curie": "UMLS:C3274504", "names": ["Phrenic Nerve Injury", "Phrenic nerve injury", "Injury of phrenic nerve", "Injury of phrenic nerve (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of phrenic nerve", "shortest_name_length": 20}
{"curie": "UMLS:C0393681", "names": ["Rhinencephalic Epilepsy", "Rhinencephalic epilepsy", "Rhinencephalic Epilepsies", "Epilepsies, Rhinencephalic", "Rhinencephalic epilepsy (disorder)", "Rhinencephalic epilepsy (diagnosis)", "epilepsy localization-related symptomatic rhinencephalic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rhinencephalic Epilepsy", "shortest_name_length": 23}
{"curie": "MONDO:0004926", "names": ["dacrocystitis", "DACROCYSTITIS", "Dacrocystitis", "dacryocystitis", "dacryoadenitis", "DACRYOCYSTITIS", "Dacryocystitis", "Dacryoadenitides", "Dacryocystitides", "Dacryocystitis NOS", "Dacryocystitis, NOS", "Dacryocystitis (disorder)", "lacrimal sac inflammation", "LACRIMAL SAC INFLAMMATION", "dacryocystitis (diagnosis)", "Unspecified dacryocystitis", "Dacryocystitis, unspecified", "inflammation of lacrimal sac", "Infection of the lacrimal sac"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dacryocystitis", "shortest_name_length": 13}
{"curie": "UMLS:C2938957", "names": ["Tumor rupture", "Tumour rupture"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tumor rupture", "shortest_name_length": 13}
{"curie": "UMLS:C5574647", "names": ["SUPRESSION ADRENAL", "adrenal supression", "adrenal suppression", "Adrenal suppression", "ADRENAL SUPPRESSION", "Suppression of adrenal gland", "Suppression of adrenal gland (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Suppression of adrenal gland", "shortest_name_length": 18}
{"curie": "UMLS:C4725707", "names": ["Extracavitary PEL", "Extracavitary Primary Effusion Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extracavitary Primary Effusion Lymphoma", "shortest_name_length": 17}
{"curie": "MONDO:0016876", "names": ["partial deletion of chromosome 11", "partial monosomy of chromosome 11", "partial deletion of chromosome type 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of chromosome 11", "shortest_name_length": 33}
{"curie": "MONDO:0013857", "names": ["alar cleft, isolated", "ALAR CLEFT, ISOLATED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alar cleft, isolated", "shortest_name_length": 20}
{"curie": "MONDO:0016576", "names": ["SHFM", "Split-hand", "Cleft hand", "Split hand", "Ectrodactyly", "FEWER digits", "ectrodactyly", "Main en griffe", "Hand ectrodactyly", "lobster-claw hand", "Lobster-claw hand", "Lobster claw hand", "Claw-hand deformity", "Claw hand deformity", "split-hand deformity", "Split-hand deformity", "Congenital cleft hand", "Claw hand deformities", "Claw-hand deformities", "Cleft hand, congenital", "lobster-claw deformity", "Lobster claw deformity", "ectrodactyly of fingers", "Ectrodactyly (disorder)", "Ectrodactyly of the hand", "Split-Hand/Foot Malformation", "split-hand/foot malformation", "split hand foot malformation", "Split hand foot malformation", "split hand-foot malformation", "Lobster-claw hand (diagnosis)", "lobster claw deformity of hand", "Congenital cleft hand (disorder)", "split hand-split foot malformation", "lobster claw deformity was observed", "Lobster-claw hand, unspecified hand", "congenital hand deformity lobster-claw", "ectrodactyly of fingers (physical finding)", "isolated split hand-split foot malformation", "Isolated split hand-split foot malformation", "lobster claw deformity of hand (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "split hand-foot malformation", "shortest_name_length": 4}
{"curie": "MONDO:0010161", "names": ["TYRSN1", "Fah deficiency", "FAH deficiency", "FAH DEFICIENCY", "Type I Tyrosinemia", "Tyrosinemia Type I", "Tyrosinemia type I", "type I tyrosinemia", "tyrosinemia type i", "Tyrosinemia Type 1", "tyrosinemia type I", "Tyrosinemia type 1", "tyrosinemia type 1", "Tyrosinemia, type I", "Tyrosinemia Type 1s", "Tyrosinaemia type I", "TYROSINEMIA, TYPE I", "tyrosinemia, type I", "Type I Tyrosinemias", "tyrosinemia, type 1", "Tyrosinemia, Type I", "Tyrosinemias, Type I", "HEPATORENAL TYROSINEMIA", "Type I Hypertyrosinemia", "Hepatorenal Tyrosinemia", "hepatorenal tyrosinemia", "Hepatorenal tyrosinemia", "Tyrosinemia, Hepatorenal", "Hepatorenal Tyrosinemias", "Hypertyrosinemia, Type I", "Type I Hypertyrosinemias", "Tyrosinemias, Hepatorenal", "Hypertyrosinemias, Type I", "Tyrosinemia type I (disorder)", "hereditary tyrosinemia type i", "Deficiency of beta-diketonase", "Fumarylacetoacetase Deficiency", "Hereditary Tyrosinemia, Type I", "Fumarylacetoacetase deficiency", "tyrosinemia type I (diagnosis)", "FUMARYLACETOACETASE DEFICIENCY", "fumarylacetoacetase deficiency", "Deficiency, Fumarylacetoacetase", "Fumarylacetoacetase Deficiencies", "Deficiency of fumarylacetoacetase", "Deficiencies, Fumarylacetoacetase", "Fumarylacetoacetase Deficiency Disease", "Deficiency Disease, Fumarylacetoacetase", "Disease, Fumarylacetoacetase Deficiency", "Fumarylacetoacetase Deficiency Diseases", "Deficiency Diseases, Fumarylacetoacetase", "Fumarylacetoacetate hydrolase deficiency", "Diseases, Fumarylacetoacetase Deficiency", "fumarylacetoacetate hydrolase deficiency", "Deficiency of fumarylacetoacetase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tyrosinemia type I", "shortest_name_length": 6}
{"curie": "MONDO:0015541", "names": ["genetic hemophagocytic syndrome", "primary hemophagocytic lymphohistiocytosis", "genetic hemophagocytic lymphohistiocytosis", "familial hemophagocytic lymphohistiocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genetic hemophagocytic lymphohistiocytosis", "shortest_name_length": 31}
{"curie": "UMLS:C5420146", "names": ["Refractory Ocular Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Ocular Melanoma", "shortest_name_length": 26}
{"curie": "UMLS:C0349458", "names": ["CIN1", "cin 1", "CIN 1", "cin i", "CIN I", "CERVICAL CANCER CIN I", "mild cervical dysplasia", "dysplasia; cervix, mild", "Mild cervical dysplasia", "Mild dysplasia of cervix", "mild cervical dysplasia (CIN I)", "dysplasia of cervix (uteri) mild", "mild cervical dysplasia (diagnosis)", "Cervical intraepithelial neoplasia I", "cervical intra-epithelial neoplasm i", "Cervical intraepithelial neoplasia grade 1", "cervix; intraepithelial neoplasia, grade I", "Low-Grade Cervix Intraepithelial Neoplasia", "Cervical intraepithelial neoplasia grade I", "cervical intraepithelial neoplasia grade 1", "neoplasia; intraepithelial, cervix, grade I", "CIN I - Cervical intraepithelial neoplasia 1", "Cervical intraepithelial neoplasia I [CIN I]", "Low Grade Cervical Intraepithelial Neoplasia", "Cervical intraepithelial neoplasia, low grade", "Low-Grade Intraepithelial Neoplasia of Cervix", "Low-Grade Cervix Uteri Intraepithelial Neoplasia", "Low-Grade Intraepithelial Neoplasia of the Cervix", "cervical intraepithelial neoplasia grade 1 (CIN-1)", "Low-Grade Uterine Cervix Intraepithelial Neoplasia", "CIN I (grade 1 cervical intraepithelial neoplasia)", "Low-Grade Intraepithelial Neoplasia of Cervix Uteri", "Cervical intraepithelial neoplasia grade 1 (disorder)", "Low-Grade Intraepithelial Neoplasia of Uterine Cervix", "Low-Grade Intraepithelial Neoplasia of the Cervix Uteri", "Low-Grade Intraepithelial Neoplasia of the Uterine Cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical intraepithelial neoplasia grade 1", "shortest_name_length": 4}
{"curie": "UMLS:C3900102", "names": ["Fibrolamellar Cancer", "Adult Fibrolamellar Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Fibrolamellar Carcinoma", "shortest_name_length": 20}
{"curie": "MONDO:0023007", "names": ["Drachtman Weinblatt Sitarz syndrome", "Marrow hypoplasia associated with congenital neurologic anomalies", "marrow hypoplasia associated with congenital neurologic anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drachtman Weinblatt Sitarz syndrome", "shortest_name_length": 35}
{"curie": "UMLS:C3805221", "names": ["Minimal Baseline Variability", "Minimal baseline fetal heart rate variability", "Minimal Baseline Fetal Heart Rate Variability", "Minimal baseline foetal heart rate variability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Minimal baseline fetal heart rate variability", "shortest_name_length": 28}
{"curie": "MONDO:0003799", "names": ["Pink eye", "Pink Eye", "pink eye", "Pink Eyes", "Madras eye", "conjunctivitis", "Conjunctivitis", "CONJUNCTIVITIS", "Pink eye disease", "Conjunctivitides", "Conjunctivitis NOS", "Conjunctivitis, NOS", "Conjunctiva inflamed", "conjunctiva inflammation", "conjunctivitis (disease)", "Conjunctivitis (disorder)", "Conjunctivitis, recurrent", "Unspecified conjunctivitis", "conjunctivitis (diagnosis)", "Conjunctivitis (recurrent)", "Inflammation of conjunctiva", "inflammation of conjunctiva", "Conjunctivitis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "conjunctivitis", "shortest_name_length": 8}
{"curie": "UMLS:C3665608", "names": ["Uterine Dehiscence", "Uterine dehiscence", "cesarean wound disruption", "Cesarean wound disruption", "Caesarean wound disruption", "Disruption of cesarean wound", "Disruption of caesarean wound", "wound; cesarean section, dehiscence", "Disruption of cesarean section wound", "Cesarean wound disruption (disorder)", "cesarean wound disruption (diagnosis)", "Disruption of caesarean section wound", "Dehiscence or disruption of uterine wound", "disruption of uterine incision after cesarean", "disruption of uterine incision after cesarean (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cesarean wound disruption", "shortest_name_length": 18}
{"curie": "UMLS:C2697368", "names": ["GI UPSET", "GI upset", "gi upset", "GI IRRITATION", "GI irritation", "Gastrointestinal upset", "UPSET GASTROINTESTINAL", "Upset gastrointestinal", "gastrointestinal upset", "gastrointestinal irritation", "Gastrointestinal irritation", "IRRITATION GASTROINTESTINAL", "Irritation gastrointestinal", "Gastrointestinal tract irritation", "Gastrointestinal irritation (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal irritation", "shortest_name_length": 8}
{"curie": "MONDO:0008827", "names": ["PPD", "PPAC", "PPRD", "SEDT-PA", "Progressive pseudorheumatoid dysplasia", "progressive pseudorheumatoid dysplasia", "PROGRESSIVE PSEUDORHEUMATOID DYSPLASIA", "progressive pseudorheumatoid chondrodysplasia", "Progressive pseudorheumatoid dysplasia (disorder)", "PROGRESSIVE PSEUDORHEUMATOID ARTHROPATHY OF CHILDHOOD", "progressive pseudorheumatoid arthropathy of childhood", "Progressive pseudorheumatoid arthropathy of childhood", "arthropathy, progressive pseudorheumatoid, of childhood", "Arthropathy, progressive pseudorheumatoid, of childhood", "ARTHROPATHY, PROGRESSIVE PSEUDORHEUMATOID, OF CHILDHOOD", "spondyloepiphyseal dysplasia tarda - progressive arthropathy", "SPONDYLOEPIPHYSEAL DYSPLASIA TARDA WITH PROGRESSIVE ARTHROPATHY", "Spondyloepiphyseal dysplasia tarda with progressive arthropathy", "spondyloepiphyseal dysplasia tarda with progressive arthropathy", "Spondyloepiphyseal dysplasia tarda-progressive arthropathy syndrome", "spondyloepiphyseal dysplasia tarda-progressive arthropathy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive pseudorheumatoid arthropathy of childhood", "shortest_name_length": 3}
{"curie": "MONDO:0017584", "names": ["Sagliker syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sagliker syndrome", "shortest_name_length": 17}
{"curie": "MONDO:0018747", "names": ["EBA", "EB acquisita", "acquired epidermolysis bullosa", "epidermolysis bullosa Aquisita", "Epidermolysis bullosa aquisita", "Acquired epidermolysis bullosa", "Acquired Epidermolysis Bullosa", "Epidermolysis Bullosa Aquisita", "epidermolysis bullosa acquisita", "Epidermolysis bullosa acquisita", "acquisita bullosa epidermolysis", "Epidermolysis Bullosa, Acquired", "Epidermolysis Bullosa Acquisita", "Epidermolysis bullosa, acquired", "epidermolysis; bullosa, acquired", "EBA - Epidermolysis bullosa acquisita", "Acquired Form of Epidermolysis Bullosa", "Acquired epidermolysis bullosa (disorder)", "acquired epidermolysis bullosa (diagnosis)", "Acquired epidermolysis bullosa, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired epidermolysis bullosa", "shortest_name_length": 3}
{"curie": "UMLS:C1335043", "names": ["Non-Neoplastic Soft Tissue Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Soft Tissue Disorder", "shortest_name_length": 35}
{"curie": "MONDO:0003909", "names": ["Bartholin Gland Adenomyoma", "Bartholin gland adenomyoma", "Bartholin's Gland Adenomyoma", "Bartholin's gland adenomyoma", "major vestibular gland adenomyoma", "adenomyoma of major vestibular gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bartholin gland adenomyoma", "shortest_name_length": 26}
{"curie": "MONDO:0002282", "names": ["WNV Infection", "Infection, WNV", "WNV Infections", "Infections, WNV", "West Nile Fever", "West Nile fever", "WEST NILE FEVER", "west nile fever", "fever; West Nile", "West Nile; fever", "West Nile fever NOS", "West Nile Fever NOS", "WN - West Nile fever", "West Nile virus infection", "West Nile Virus Infection", "West Nile fever (diagnosis)", "West Nile Fever, unspecified", "Disease due to West Nile virus", "Disease caused by West Nile virus", "West Nile virus infectious disease", "West Nile virus disease or disorder", "West Nile virus caused disease or disorder", "Disease caused by West Nile virus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "West Nile fever", "shortest_name_length": 13}
{"curie": "MONDO:0044649", "names": ["Gershoni-Baruch syndrome", "omphalocele-diaphragmatic hernia-cardiovascular anomalies-radial ray defect syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "omphalocele-diaphragmatic hernia-cardiovascular anomalies-radial ray defect syndrome", "shortest_name_length": 24}
{"curie": "UMLS:C0236068", "names": ["tongue swell", "swells tongue", "Swollen tongue", "Tongue swollen", "Swollen;tongue", "tongue swollen", "swollen tongue", "tongue swelling", "Tongue swelling", "swelling tongue", "TONGUE SWELLING", "swollen tongues", "swelling of tongue", "Swelling of tongue", "Swelling of the tongue", "swollen tongue (symptom)", "Tongue swelling (finding)", "Tongue swelling non-specific", "TONGUE SWELLING NON-SPECIFIC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tongue swelling", "shortest_name_length": 12}
{"curie": "UMLS:C1709447", "names": ["Tis (Paget)", "Tis (Paget's)", "Breast Paget Disease without Invasive Carcinoma", "Paget Disease of the Breast without Invasive Carcinoma", "Paget's Disease of the Breast without Invasive Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Paget Disease without Invasive Carcinoma", "shortest_name_length": 11}
{"curie": "UMLS:C4054225", "names": ["Churg-Strauss Syndrome Associated Glomerulonephritis", "Pauci-Immune Glomerulonephritis associated with Eosinophilic Granulomatosis with Polyangiitis", "Pauci-immune Glomerulonephritis associated with Eosinophilic Granulomatosis with Polyangiitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pauci-Immune Glomerulonephritis associated with Eosinophilic Granulomatosis with Polyangiitis", "shortest_name_length": 52}
{"curie": "UMLS:C0406479", "names": ["acne steroid", "Steroid acne", "Acne steroid", "acne steroids", "Acne steroid-induced", "Steroid acne (disorder)", "Steroid acne (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Steroid acne", "shortest_name_length": 12}
{"curie": "MONDO:0004827", "names": ["esophagus squamous papilloma", "Esophageal Squamous Papilloma", "esophageal squamous papilloma", "Esophageal squamous papilloma", "Esophagus Squamous Cell Papilloma", "esophagus squamous cell papilloma", "Esophageal Squamous Cell Papilloma", "Squamous Cell Papilloma of Esophagus", "squamous cell papilloma of esophagus", "Squamous cell papilloma of esophagus", "Squamous cell papilloma of oesophagus", "squamous cell papilloma of the esophagus", "Squamous Cell Papilloma of the Esophagus", "Squamous cell papilloma of esophagus (disorder)", "squamous cell papilloma of esophagus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophagus squamous cell papilloma", "shortest_name_length": 28}
{"curie": "MONDO:0035344", "names": ["ABE", "Acute kernicterus", "acute bilirubin encephalopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute bilirubin encephalopathy", "shortest_name_length": 3}
{"curie": "UMLS:C5418787", "names": ["Locally Advanced Rectal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Rectal Carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0016715", "names": ["ETMR", "ETANTR", "ependymoblastoma", "Ependymoblastoma", "Ependymoblastomas", "ETMR, C19MC-altered", "ETMR, C19MC-Altered", "Ependymoblastoma (disorder)", "neuroectodermal tumors primitive", "ependymoblastoma; unspecified site", "embryonal tumor with Multilayered Rosettes", "Embryonal Tumor with Multilayered Rosettes", "embryonal tumor with abundant neuropil and true rosettes", "Embryonal tumor with multilayered rosettes C19MC-altered", "Embryonal Tumor with Abundant Neuropil and True Rosettes", "embryonal tumor with abundant neuropil and true Rosettes", "Embryonal tumor with abundant neuropil and true rosettes", "embryonal tumor with Multilayered Rosettes, C19MC-altered", "Embryonal Tumor with Multilayered Rosettes, C19MC-Altered", "embryonal tumor with multilayered rosettes, C19MC-altered", "Embryonal tumour with abundant neuropil and true rosettes", "embryonal tumor with Multilayered Rosettes with C19MC amplification", "Embryonal Tumor with Multilayered Rosettes with C19MC Amplification"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ependymoblastoma", "shortest_name_length": 4}
{"curie": "MONDO:0004715", "names": ["stage 0 liver carcinoma", "liver carcinoma in situ", "liver in situ carcinoma", "carcinoma in situ of liver", "Carcinoma in situ of liver", "Hepatobiliary cancer in situ", "Hepatobiliary carcinoma in situ", "Carcinoma in situ of liver, NOS", "liver neoplasm carcinoma in situ", "Hepatobiliary carcinoma in situ NOS", "Hepato-biliary carcinoma in situ NOS", "Carcinoma in situ of liver (disorder)", "carcinoma in situ of liver (diagnosis)", "carcinoma in situ of liver and biliary system", "Carcinoma in situ of liver and biliary system", "Carcinoma in situ of liver and/or biliary system", "Carcinoma in situ of liver, gallbladder and bile ducts", "carcinoma in situ of liver, gallbladder and bile ducts", "Carcinoma in situ of liver and/or biliary system (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "liver carcinoma in situ", "shortest_name_length": 23}
{"curie": "MONDO:0024238", "names": ["Brain degeneration", "degeneration; brain", "brain; degeneration", "Cerebral degeneration", "cerebral degeneration", "CEREBRAL DEGENERATION", "Degeneration;cerebral", "cerebral degenerations", "Degeneration of cerebrum", "Cerebral degeneration, NOS", "Degenerative brain disorder", "degenerative brain disorder", "brain degenerative disorders", "Cerebral degeneration (disorder)", "cerebral degeneration (diagnosis)", "Cerebral degeneration, unspecified", "Neuroaxonal degeneration in the brain", "Degenerative brain disorder (disorder)", "telencephalon neurodegenerative disease", "degenerative brain disorder (diagnosis)", "neurodegenerative disease of telencephalon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral degeneration", "shortest_name_length": 18}
{"curie": "MONDO:0013166", "names": ["ABAT", "GABAT", "GABA-T deficiency", "GABA transferase deficiency", "GABA-TRANSAMINASE DEFICIENCY", "GABA-transaminase deficiency", "GABA transaminase deficiency", "Gaba-Transaminase Deficiency", "GABA aminotransferase deficiency", "GABA aminotransaminase deficiency", "gamma aminobutyrate transaminase deficiency", "Gamma-aminobutyrate transaminase deficiency", "Gamma aminobutyrate transaminase deficiency", "4 alpha aminobutyrate transaminase deficiency", "gamma-aminobutyric acid transaminase deficiency", "Gamma aminobutyric acid transaminase deficiency", "Gamma-aminobutyric acid transaminase deficiency", "gamma aminobutyric acid transaminase deficiency", "gamma-amino butyric acid transaminase deficiency", "Gamma-amino butyric acid transaminase deficiency", "Gamma-aminobutyric acid transaminase deficiency (disorder)", "gamma-aminobutyric acid transaminase deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "GABA aminotransaminase deficiency", "shortest_name_length": 4}
{"curie": "UMLS:C0586358", "names": ["BilIN", "Biliary dysplasia", "Biliary Dysplasia", "Biliary tract dysplasia", "Biliary Intraepithelial Neoplasia", "Biliary tract dysplasia (disorder)", "Biliary System Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Biliary Intraepithelial Neoplasia", "shortest_name_length": 5}
{"curie": "UMLS:C0264233", "names": ["sinus; mucocele", "mucocele; sinus", "nasal sinus mucocele", "Nasal sinus mucocele", "Nasal Sinus Mucocele", "mucocele; nasal sinus", "nasal sinus; mucocele", "Mucocele of Nasal Sinus", "Paranasal sinus mucocele", "Accessory Sinus Mucocele", "Paranasal Sinus Mucocele", "Paranasal sinus mucocoele", "Mucous cyst of nasal sinus", "Mucocele of Paranasal Sinus", "Mucocele of the Nasal Sinus", "Mucocele of Accessory Sinus", "Mucocele of the Paranasal Sinus", "Mucocele of the Accessory Sinus", "nasal sinus mucocele (diagnosis)", "Mucous cyst of nasal sinus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasal sinus mucocele", "shortest_name_length": 15}
{"curie": "UMLS:C0151595", "names": ["DIGITALIS INTOXICATION", "Digitalis intoxication", "DIGITALIS INTOXICATION (NOS)", "Digitalis intoxication (NOS)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Digitalis intoxication", "shortest_name_length": 22}
{"curie": "UMLS:C0861571", "names": ["Stage 0 Mouth Epidermoid Carcinoma", "Mouth Epidermoid Carcinoma in situ", "Epidermoid Carcinoma in situ of Mouth", "Mouth Squamous Cell Carcinoma in situ", "Stage 0 Epidermoid Carcinoma of Mouth", "Squamous Cell Carcinoma in situ of Mouth", "Stage 0 Squamous Cell Carcinoma of Mouth", "Stage 0 Oral Cavity Squamous Cell Cancer", "Stage 0 Oral Cavity Epidermoid Carcinoma", "Oral Cavity Epidermoid Carcinoma in situ", "Epidermoid Carcinoma in situ of the Mouth", "Stage 0 Epidermoid Carcinoma of the Mouth", "Stage 0 Oral Cavity Squamous Cell Carcinoma", "Epidermoid Carcinoma in situ of Oral Cavity", "Oral Cavity Squamous Cell Carcinoma in situ", "Stage 0 Epidermoid Carcinoma of Oral Cavity", "Stage 0 Squamous Cell Carcinoma of the Mouth", "Squamous Cell Carcinoma in situ of the Mouth", "Squamous Cell Carcinoma in situ of Oral Cavity", "Stage 0 Squamous Cell Carcinoma of Oral Cavity", "Stage 0 Epidermoid Carcinoma of the Oral Cavity", "Epidermoid Carcinoma in situ of the Oral Cavity", "Squamous cell carcinoma of the oral cavity stage 0", "Stage 0 Squamous Cell Carcinoma of the Oral Cavity", "Squamous Cell Carcinoma in situ of the Oral Cavity", "Stage 0 Oral Cavity Squamous Cell Carcinoma AJCC v6", "Stage 0 Oral Cavity Squamous Cell Carcinoma AJCC v7", "Stage 0 Oral Cavity Squamous Cell Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Oral Cavity Squamous Cell Carcinoma AJCC v6 and v7", "shortest_name_length": 34}
{"curie": "MONDO:0030036", "names": ["LEMSPAD", "LEMSPAD SYNDROME", "Lemspad Syndrome", "leukoencephalopathy, motor delay, spasticity, and dysarthria syndrome", "LEUKOENCEPHALOPATHY, MOTOR DELAY, SPASTICITY, AND DYSARTHRIA SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukoencephalopathy, motor delay, spasticity, and dysarthria syndrome", "shortest_name_length": 7}
{"curie": "MONDO:0035648", "names": ["Juvenile-onset Steinert disease", "Juvenile-onset myotonic dystrophy type 1", "juvenile-onset Steinert myotonic dystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile-onset Steinert myotonic dystrophy", "shortest_name_length": 31}
{"curie": "UMLS:C0494463", "names": ["Alzheimer; late onset", "late onset; Alzheimer", "Late Onset Alzheimer Disease", "Alzheimer Disease, Late Onset", "Late onset Alzheimer's disease", "Alzheimer's disease with late onset", "SDAT - Senile dementia, Alzheimer's type", "Dementia in Alzheimer's disease - type 1", "Dementia of the Alzheimers type, late onset", "Dementia in Alzheimer's disease with late onset", "Primary degenerative dementia of the Alzheimer type, late onset", "Primary degenerative dementia of the Alzheimer type, senile onset", "Primary degenerative dementia of the Alzheimer type, senile onset (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alzheimer Disease, Late Onset", "shortest_name_length": 21}
{"curie": "MONDO:0015704", "names": ["familial scaphocephaly syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial scaphocephaly syndrome", "shortest_name_length": 31}
{"curie": "UMLS:C0555199", "names": ["Polar Spongioblastoma", "Polar spongioblastoma", "Spongioblastoma polare", "Spongioblastoma, Polar", "Polar Spongioblastomas", "Spongioblastomas, Polar", "Primitive polar spongioblastoma", "spongioblastoma; polare, unspecified site", "polare; spongioblastoma, unspecified site", "Polar spongioblastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spongioblastoma, Polar", "shortest_name_length": 21}
{"curie": "MONDO:0018241", "names": ["primary short bowel syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary short bowel syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0010642", "names": ["Lesch-Nyhan phenotype with normal HGPRT", "LESCH-NYHAN PHENOTYPE WITH NORMAL HGPRT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lesch-Nyhan phenotype with normal HGPRT", "shortest_name_length": 39}
{"curie": "MONDO:0004214", "names": ["Ovarian Endometrioid Cystadenofibroma", "ovarian endometrioid cystadenofibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian endometrioid cystadenofibroma", "shortest_name_length": 37}
{"curie": "MONDO:0008021", "names": ["CS", "CPD6", "CWS1", "Cowden syndrome 1", "PTEN Cowden disease", "Proteus-like syndrome", "Cowden syndrome type 1", "Lhermitte-Duclos disease", "Lhermitte-Duclos syndrome", "multiple hamartoma syndrome", "cerebelloparenchymal disorder 6", "CEREBELLOPARENCHYMAL DISORDER VI", "Cerebelloparenchymal Disorder VI", "Cowden disease caused by mutation in PTEN", "dysplastic gangliocytoma of the cerebellum", "Pten Hamartoma Tumor Syndrome With Granular Cell Tumor", "cerebellar granule cell Hypertrophy and megalencephaly", "Cerebellar Granule Cell Hypertrophy and Megalencephaly", "CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY", "PTEN HAMARTOMA TUMOR SYNDROME WITH GRANULAR CELL TUMOR"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cowden syndrome 1", "shortest_name_length": 2}
{"curie": "UMLS:C1334432", "names": ["LR GIST", "Low Risk GIST", "Low Risk Gastrointestinal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Risk Gastrointestinal Stromal Tumor", "shortest_name_length": 7}
{"curie": "MONDO:0007312", "names": ["CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM", "Charcot-Marie-Tooth disease with ptosis and parkinsonism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease with ptosis and parkinsonism", "shortest_name_length": 56}
{"curie": "MONDO:0001892", "names": ["spine lymphoma", "lymphoma spine", "SPINE LYMPHOMA", "spinal cord cancer", "Spinal Cord Lymphoma", "spinal cord lymphoma", "Lymphoma of Spinal Cord", "lymphoma of spinal cord", "lymphoma of the spinal cord", "Lymphoma of the Spinal Cord", "Primary Spinal Cord Lymphoma", "primary spinal cord lymphoma", "lymphoma of spinal cord (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal cord lymphoma", "shortest_name_length": 14}
{"curie": "MONDO:0100488", "names": ["LBC", "HDGC", "DGLBC", "gastric cancer, hereditary diffuse", "diffuse gastric and lobular breast cancer syndrome", "gastric cancer, familial diffuse breast cancer, lobular", "CDH1-related diffuse gastric and lobular breast cancer syndrome", "DIFFUSE GASTRIC AND LOBULAR BREAST CANCER SYNDROME WITH CLEFT LIP AND WITH OR WITHOUT CLEFT PALATE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CDH1-related diffuse gastric and lobular breast cancer syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0012458", "names": ["Hyt5", "HYT5", "HYPERTENSION, ESSENTIAL, BODY MASS-RELATED", "hypertension, essential, body Mass-related", "hypertension, essential, susceptibility to, 5", "HYPERTENSION, ESSENTIAL, SUSCEPTIBILITY TO, 5", "hypertension, essential, susceptibility to, type 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertension, essential, susceptibility to, 5", "shortest_name_length": 4}
{"curie": "MONDO:0006239", "names": ["head and neck paraganglioma", "Head and Neck Paraganglioma", "Paragangliomas, head and neck", "paraganglioma of head and neck", "Paraganglioma of Head and Neck", "Paraganglioma of head and neck", "Paraganglioma of the Head and Neck", "paraganglioma of the head and neck", "craniocervical region paraganglioma", "paraganglioma of craniocervical region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "head and neck paraganglioma", "shortest_name_length": 27}
{"curie": "UMLS:C2717860", "names": ["Encapsulating Peritoneal Scleroses", "Encapsulating Peritoneal Sclerosis", "Encapsulating peritoneal sclerosis", "Peritoneal Sclerosis, Encapsulating", "Sclerosis, Encapsulating Peritoneal", "Scleroses, Encapsulating Peritoneal", "Peritoneal Scleroses, Encapsulating"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Encapsulating Peritoneal Sclerosis", "shortest_name_length": 34}
{"curie": "MONDO:0023147", "names": ["fetal parainfluenza virus type 3 syndrome", "Human respirovirus 3 infectious embryofetopathy", "Human respirovirus 3 caused infectious embryofetopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fetal parainfluenza virus type 3 syndrome", "shortest_name_length": 41}
{"curie": "UMLS:C4329635", "names": ["Central Nervous System Mature T-Cell and NK-Cell Non-Hodgkin Lymphoma", "Mature T-Cell and NK-Cell Non-Hodgkin Lymphoma of the Central Nervous System", "Primary Central Nervous System Mature T-Cell and NK-Cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Mature T-Cell and NK-Cell Non-Hodgkin Lymphoma", "shortest_name_length": 69}
{"curie": "MONDO:0020781", "names": ["PEBEL1", "NAD(P)HX epimerase deficiency", "encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy", "encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1", "ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1", "shortest_name_length": 6}
{"curie": "UMLS:C0161823", "names": ["Traumatic Neuroma", "Traumatic neuroma", "NEUROMA, TRAUMATIC", "Traumatic neuroma (disorder)", "Aberrant regeneration of nerve", "Traumatic neuroma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Traumatic neuroma", "shortest_name_length": 17}
{"curie": "MONDO:0015539", "names": ["progressive nodular histiocytosis", "Progressive nodular histiocytosis", "Progressive nodular histiocytosis (disorder)", "Progressive nodular histiocytosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive nodular histiocytosis", "shortest_name_length": 33}
{"curie": "UMLS:C5419162", "names": ["COVID-19 Symptomatic Laboratory-Confirmed", "Symptomatic COVID-19 Infection Laboratory-Confirmed", "Symptomatic SARS-CoV-2 Infection Laboratory-Confirmed"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Symptomatic COVID-19 Infection Laboratory-Confirmed", "shortest_name_length": 41}
{"curie": "MONDO:0030027", "names": ["ETM6", "essential tremor 6", "TREMOR, HEREDITARY ESSENTIAL 6", "tremor, hereditary essential, 6", "TREMOR, HEREDITARY ESSENTIAL, 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tremor, hereditary essential, 6", "shortest_name_length": 4}
{"curie": "MONDO:0019181", "names": ["non-specific X-linked mental retardation", "Mental Retardation, X-Linked Nonsyndromic", "isolated X-linked intellectual disability", "mental retardation, nonsyndromic, X-linked", "mental retardation, X-linked, nonsyndromic", "non-specific X-linked intellectual disability", "X-linked non-specific intellectual disability", "nonsyndromic X-linked intellectual disability", "X-linked non-syndromic intellectual disability", "non-syndromic X-linked intellectual disability", "non-syndromic intellectual disability, X-linked", "intellectual disability, X-linked, nonsyndromic", "intellectual disability, nonsyndromic, X-linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-syndromic X-linked intellectual disability", "shortest_name_length": 40}
{"curie": "MONDO:0060611", "names": ["CIMAH", "METHYLENETETRAHYDROFOLATE DEHYDROGENASE 1 DEFICIENCY", "methylenetetrahydrofolate dehydrogenase 1 deficiency", "COMBINED IMMUNODEFICIENCY AND MEGALOBLASTIC ANEMIA WITH OR WITHOUT HYPERHOMOCYSTEINEMIA", "combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia", "shortest_name_length": 5}
{"curie": "MONDO:0014818", "names": ["NPHS13", "nephrotic syndrome type 13", "nephrotic syndrome, type 13", "NEPHROTIC SYNDROME, TYPE 13", "NUP205 familial nephrotic syndrome", "nephrotic syndrome, type 13; NPHS13", "familial nephrotic syndrome caused by mutation in NUP205"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrotic syndrome, type 13", "shortest_name_length": 6}
{"curie": "UMLS:C4761205", "names": ["Hyperesthesia teeth", "Hyperaesthesia teeth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyperesthesia teeth", "shortest_name_length": 19}
{"curie": "MONDO:0008438", "names": ["SPG4", "FSP2", "spastic paraplegia 4", "SPASTIC PARAPLEGIA 4", "Spastic Paraplegia 4", "Spastic Paraplegia Type 4", "hereditary spastic paraplegia 4", "SPAST hereditary spastic paraplegia", "hereditary spastic paraplegia type 4", "autosomal dominant spastic paraplegia 4", "Spastic paraplegia 4, autosomal dominant", "SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT", "spastic paraplegia 4, autosomal dominant", "Autosomal dominant, spastic paraplegia 4", "autosomal dominant spastic paraplegia type 4", "Autosomal dominant spastic paraplegia type 4", "Familial spastic paraplegia autosomal dominant 2", "familial spastic paraplegia autosomal dominant 2", "FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 2", "familial spastic paraplegia, autosomal dominant, 2", "Familial Spastic Paraplegia, Autosomal Dominant, 2", "familial spastic paraplegia autosomal dominant type 4", "Autosomal dominant spastic paraplegia type 4 (disorder)", "Autosomal dominant spastic paraplegia type 4 (diagnosis)", "hereditary spastic paraplegia caused by mutation in SPAST"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 4", "shortest_name_length": 4}
{"curie": "MONDO:0019012", "names": ["ACPS2", "ACPS II", "Carpenter", "Carpenter syndrome", "carpenter syndrome", "Carpenter Syndrome", "CARPENTER SYNDROME", "carpenters syndrome", "Carpenter's syndrome", "carpenter's syndrome", "Carpenter 's Syndrome", "Carpenter 's syndrome", "acrocephalopolysyndactyly 2", "acrocephalosyndactyly, type II", "Acrocephalopolysyndactyly type 2", "acrocephalopolysyndactyly type 2", "acrocephalopolysyndactyly type II", "Acrocephalopolysyndactyly Type II", "Type II Acrocephalopolysyndactyly", "Acrocephalopolysyndactyly type II", "ACROCEPHALOPOLYSYNDACTYLY TYPE II", "type II Acrocephalopolysyndactyly", "acrocephalopolysyndactyly 2 (ACPS 2)", "Acrocephalopolysyndactyly type II (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carpenter syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0012172", "names": ["TFPD", "MTPD", "TFP deficiency", "TFP Deficiency", "LCHAD Deficiency", "Trifunctional enzyme deficiency", "Trifunctional protein deficiency", "Trifunctional Protein Deficiency", "TRIFUNCTIONAL PROTEIN DEFICIENCY", "trifunctional Protein deficiency", "Human trifunctional protein deficiency", "mitochondrial trifunctional protein deficiency", "Mitochondrial trifunctional protein deficiency", "mitochondrial trifunctional PROTEIN deficiency", "Mitochondrial Trifunctional Protein Deficiency", "MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY", "Decreased 3-hydroxyacyl-CoA dehydrogenase level", "Long-Chain 3-OH Acyl-CoA Dehydrogenase Deficiency", "Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency", "Long chain 3 hydroxyacyl coA dehydrogenase deficiency", "Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency", "Short chain 3-hydroxyacyl-CoA dehydrogenase deficiency", "Long-Chain 3-Hydroxy Acyl CoA Dehydrogenase Deficiency", "3-Hydroxyacyl-CoA Dehydrogenase, Long Chain, Deficiency", "Long-chain L-3 hydroxyacyl-CoA dehydrogenase deficiency", "Mitochondrial trifunctional protein deficiency (disorder)", "trifunctional Protein deficiency with myopathy and neuropathy", "LCHAD - Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency", "Short-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency", "Short chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency", "TRIFUNCTIONAL PROTEIN DEFICIENCY WITH MYOPATHY AND NEUROPATHY", "Trifunctional Protein Deficiency With Myopathy And Neuropathy", "Short chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (disorder)", "Medium and short-chain L-3-hydroxyacyl-coenzyme A dehydrogenase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial trifunctional protein deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0011583", "names": ["HCHWAD", "APP-related cerebral amyloid angiopathy", "cerebral amyloid angiopathy, APP-related", "Cerebral Amyloid Angiopathy, APP-Related", "CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED", "Cerebral Amyloid Angiopathy, App-Related", "Amyloidosis, Cerebroarterial, App-Related", "AMYLOIDOSIS, CEREBROARTERIAL, APP-RELATED", "amyloidosis, Cerebroarterial, APP-related", "CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, IOWA VARIANT", "Cerebral Amyloid Angiopathy, App-Related, Iowa Variant", "cerebral amyloid angiopathy, APP-related, Iowa variant", "Cerebral Amyloid Angiopathy, App-Related, Dutch Variant", "cerebral amyloid angiopathy, APP-related, Dutch variant", "CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT", "cerebral amyloid angiopathy, APP-related, Arctic variant", "Cerebral Amyloid Angiopathy, App-Related, Arctic Variant", "CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ITALIAN VARIANT", "cerebral amyloid angiopathy, APP-related, Flemish variant", "CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, FLEMISH VARIANT", "Cerebral Amyloid Angiopathy, App-Related, Italian Variant", "cerebral amyloid angiopathy, APP-related, Italian variant", "Cerebral Amyloid Angiopathy, App-Related, Flemish Variant", "Hereditary Cerebral Hemorrhage with Amyloidosis-Dutch Type", "amyloidosis, hereditary, with cerebral hemorrhage, Dutch variant", "Amyloidosis, Hereditary, With Cerebral Hemorrhage, Dutch Variant", "cerebral amyloid angiopathy, Dutch, Italian, Iowa, Flemish, Arctic variants"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral amyloid angiopathy, APP-related", "shortest_name_length": 6}
{"curie": "UMLS:C5419745", "names": ["Recurrent Kidney Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Kidney Carcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0021537", "names": ["nasopharynx lymphoepithelioma", "Nasopharyngeal Lymphoepithelioma", "lymphoepithelioma of nasopharynx", "Lymphoepithelioma of Nasopharynx", "nasopharyngeal lymphoepithelioma", "lymphoepithelioma, nasopharyngeal", "lymphoepithelioma of the nasopharynx", "Lymphoepithelioma of the Nasopharynx", "nasopharynx undifferentiated carcinoma", "Undifferentiated nasopharyngeal carcinoma", "Undifferentiated Carcinoma of Nasopharynx", "Nasopharyngeal Undifferentiated Carcinoma", "nasopharyngeal undifferentiated carcinoma", "undifferentiated carcinoma of nasopharynx", "Undifferentiated carcinoma of nasopharynx", "Nasopharyngeal Lymphoepithelial Carcinoma", "undifferentiated carcinoma of the nasopharynx", "Undifferentiated Nasopharyngeal Throat Cancer", "undifferentiated nasopharyngeal throat cancer", "Undifferentiated Carcinoma of the Nasopharynx", "Undifferentiated carcinoma of nasopharynx (disorder)", "undifferentiated carcinoma of nasopharynx (diagnosis)", "nasopharyngeal nonkeratinizing undifferentiated carcinoma", "Nasopharyngeal Nonkeratinizing Undifferentiated Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "undifferentiated carcinoma of nasopharynx", "shortest_name_length": 29}
{"curie": "UMLS:C4053530", "names": ["CNH", "Cutaneous Neurocristic Hamartoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous Neurocristic Hamartoma", "shortest_name_length": 3}
{"curie": "MONDO:0011774", "names": ["DFNB30", "autosomal recessive deafness 30", "deafness, autosomal recessive 30", "Deafness, Autosomal Recessive 30", "DEAFNESS, AUTOSOMAL RECESSIVE 30", "deafness, autosomal recessive type 30", "autosomal recessive nonsyndromic deafness 30", "MYO3A autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 30", "autosomal recessive nonsyndromic deafness type 30", "autosomal recessive nonsyndromic deafness caused by mutation in MYO3A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 30", "shortest_name_length": 6}
{"curie": "MONDO:0004421", "names": ["Sclerosing Breast Papilloma", "sclerosing breast papilloma", "Breast Sclerosing Papilloma", "Complex Sclerosing Papillary Lesion", "Complex sclerosing papillary lesion", "Complex sclerosing papillary lesion of the breast", "Complex Sclerosing Papillary Lesion of the Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sclerosing breast papilloma", "shortest_name_length": 27}
{"curie": "UMLS:C0346216", "names": ["Malignant tumor of seminal vesicle", "Malignant Seminal Vesicle Neoplasm", "malignant tumor of seminal vesicle", "Malignant tumour of seminal vesicle", "Malignant neoplasm of seminal vesicle", "malignant neoplasm of seminal vesicle", "Malignant tumor of seminal vesicle (disorder)", "malignant neoplasm of seminal vesicle (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant tumor of seminal vesicle", "shortest_name_length": 34}
{"curie": "MONDO:0001272", "names": ["Functional diarrhea", "functional diarrhea", "Diarrhoea;functional", "functional; diarrhea", "Functional diarrhoea", "functional diarrhoea", "diarrhea; functional", "Functional diarrhea (disorder)", "functional diarrhea (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "functional diarrhea", "shortest_name_length": 19}
{"curie": "UMLS:C5420646", "names": ["Unresectable Vulvar Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Vulvar Carcinoma", "shortest_name_length": 29}
{"curie": "UMLS:C0234962", "names": ["PULMONARY VASCULITIS", "Pulmonary vasculitis", "VASCULITIS PULMONARY", "Vasculitis pulmonary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pulmonary vasculitis", "shortest_name_length": 20}
{"curie": "MONDO:0015426", "names": ["DBQD", "DESBUQUOIS SYNDROME", "desbuquois syndrome", "Desbuquois syndrome", "Desbuquois dysplasia", "Desbuquois Dysplasia", "Desbuquois syndrome (disorder)", "Micromelic Dwarfism With Vertebral And Metaphyseal Abnormalities And Advanced Carpotarsal Ossification", "micromelic dwarfism with vertebral and metaphyseal abnormalities and advanced carpotarsal ossification", "MICROMELIC DWARFISM WITH VERTEBRAL AND METAPHYSEAL ABNORMALITIES AND ADVANCED CARPOTARSAL OSSIFICATION", "micromelic dwarfism, narrow chest, vertebral and metaphyseal abnormalities and advanced carpotarsal ossification"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Desbuquois dysplasia", "shortest_name_length": 4}
{"curie": "MONDO:0003029", "names": ["Skin Angiosarcoma", "Skin angiosarcoma", "skin angiosarcoma", "Skin Hemangiosarcoma", "skin hemangiosarcoma", "angiosarcoma of skin", "Angiosarcoma of Skin", "Angiosarcoma of skin", "Dermal hemangiosarcoma", "Cutaneous Angiosarcoma", "Hemangiosarcoma of Skin", "Hemangiosarcoma of skin", "hemangiosarcoma of skin", "angiosarcoma of the skin", "Angiosarcoma of the Skin", "Cutaneous hemangiosarcoma", "hemangiosarcoma of the skin", "Hemangiosarcoma of the Skin", "Angiosarcoma of skin (disorder)", "angiosarcoma of skin (diagnosis)", "Hemangiosarcoma of skin (disorder)", "zone of skin angiosarcoma (disease)", "hemangiosarcoma of skin (diagnosis)", "angiosarcoma (disease) of zone of skin", "malignant neoplasm sarcoma angiosarcoma of skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin angiosarcoma", "shortest_name_length": 17}
{"curie": "MONDO:0010985", "names": ["FAME1", "FCMTE1", "BAFME1", "Cortical Tremor, Familial", "familial adult myoclonic epilepsy 1", "epilepsy, familial ADULT myoclonic, 1", "Epilepsy, Familial Adult Myoclonic, 1", "epilepsy, familial adult myoclonic, 1", "EPILEPSY, FAMILIAL ADULT MYOCLONIC, 1", "Benign Adult Familial Myoclonic Epilepsy 1", "benign adult familial myoclonic epilepsy 1", "BENIGN ADULT FAMILIAL MYOCLONIC EPILEPSY 1", "familial cortical myoclonic tremor and epilepsy 1", "Cortical Myoclonic Tremor With Epilepsy, Familial", "Epilepsy, Myoclonic, Benign Adult Familial, Type 1", "cortical myoclonic tremor with epilepsy, familial, 1", "CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, familial adult myoclonic, 1", "shortest_name_length": 5}
{"curie": "UMLS:C1263758", "names": ["Female genital tract infection", "female genital tract disorder infection", "Female genital tract infection (disorder)", "Female genital tract infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Female genital tract infection", "shortest_name_length": 30}
{"curie": "MONDO:0100407", "names": ["AML, t(11;15)(p15;q35)", "acute myeloid leukemia, t(11;15)(p15;q35)", "AML with t(11;15)(p15;q35); NUP98-JARID1A", "Acute Myeloid Leukemia with t(11;15)(p15;q35); NUP98-JARID1A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, t(11;15)(p15;q35)", "shortest_name_length": 22}
{"curie": "MONDO:0000509", "names": ["isolated intellectual disability", "nonsyndromic intellectual disability", "non-syndromic intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-syndromic intellectual disability", "shortest_name_length": 32}
{"curie": "MONDO:0001214", "names": ["Acute conjunctivitis", "conjunctivitis acute", "Acute Conjunctivitis", "acute conjunctivitis", "acute; conjunctivitis", "conjunctivitis; acute", "Acute conjunctivitis, NOS", "acute conjunctivitis (disease)", "conjunctivitis (disease), acute", "Acute conjunctivitis (disorder)", "acute conjunctivitis (diagnosis)", "Unspecified acute conjunctivitis", "Other mucopurulent conjunctivitis", "Acute conjunctivitis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute conjunctivitis", "shortest_name_length": 20}
{"curie": "MONDO:0012369", "names": ["SLEB6", "SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 6", "systemic lupus erythematosus, susceptibility to, 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "systemic lupus erythematosus, susceptibility to, 6", "shortest_name_length": 5}
{"curie": "MONDO:0003728", "names": ["Breast Fibrosarcoma", "breast fibrosarcoma", "fibrosarcoma of breast", "Fibrosarcoma of Breast", "Fibrosarcoma of the breast", "Fibrosarcoma of the Breast", "fibrosarcoma of the breast", "breast fibrosarcoma (disease)", "fibrosarcoma of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast fibrosarcoma", "shortest_name_length": 19}
{"curie": "MONDO:0008165", "names": ["SAO", "EL4", "sao", "Elliptocytosis 4", "he, stomatocytic", "ELLIPTOCYTOSIS 4", "elliptocytosis 4", "HE, STOMATOCYTIC", "ovalocytosis, SA type", "Hereditary ovalocytosis", "Melanesian ovalocytosis", "hereditary ovalocytosis", "Stomatocytic ovalocytosis", "Melanesian elliptocytosis", "stomatocytic elliptocytosis", "Stomatocytic elliptocytosis", "southeast Asian ovalocytosis", "Southeast Asian ovalocytosis", "OVALOCYTOSIS, SOUTHEAST ASIAN", "ovalocytosis, southeast Asian", "Ovalocytosis, Hereditary Hemolytic", "ovalocytosis, hereditary hemolytic", "ELLIPTOCYTOSIS, STOMATOCYTIC HEREDITARY", "elliptocytosis, stomatocytic hereditary", "Southeast Asian ovalocytosis (disorder)", "OVALOCYTOSIS, MALAYSIAN-MELANESIAN-FILIPINO TYPE", "ovalocytosis, Malaysian-Melanesian-Filipino type", "Ovalocytosis, Malaysian-Melanesian-Filipino Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "southeast Asian ovalocytosis", "shortest_name_length": 3}
{"curie": "MONDO:0016289", "names": ["cervical germ cell cancer", "germ cell cancer of cervix uteri", "cervical malignant germ cell tumor", "germ cell cancer of the cervix uteri", "uterine cervix malignant germ cell tumor", "malignant germ cell tumor of cervix uteri", "malignant germ cell tumor of the cervix uteri"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant germ cell tumor of cervix uteri", "shortest_name_length": 25}
{"curie": "MONDO:0009209", "names": ["Aarskog-Like Syndrome", "Aarskog-like syndrome", "AARSKOG-LIKE SYNDROME", "Teebi Naguib Alawadi syndrome", "Teebi-Naguib-Alawadi syndrome", "Faciodigitogenital Syndrome, Recessive", "KUWAIT-TYPE FACIODIGITOGENITAL SYNDROME", "Kuwait Type Faciodigitogenital Syndrome", "Kuwait type faciodigitogenital syndrome", "Facio-digito-genital syndrome Kuwait type", "Facio-digito-genital syndrome, Kuwait type", "facio-digito-genital syndrome, Kuwait type", "Autosomal recessive faciodigitogenital syndrome", "autosomal recessive faciodigitogenital syndrome", "FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE", "faciodigitogenital syndrome, autosomal recessive", "Autosomal recessive facio-digito-genital syndrome", "Autosomal recessive faciodigitogenital syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive faciodigitogenital syndrome", "shortest_name_length": 21}
{"curie": "MONDO:0003286", "names": ["Extrahepatic Bile Duct Leiomyoma", "extrahepatic bile duct leiomyoma", "Leiomyoma of Extrahepatic Bile Duct", "leiomyoma of extrahepatic bile duct", "Leiomyoma of the Extrahepatic Bile Duct", "leiomyoma of the extrahepatic bile duct", "leiomyoma of extrahepatic bile duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extrahepatic bile duct leiomyoma", "shortest_name_length": 32}
{"curie": "MONDO:0009790", "names": ["OPTICOCOCHLEODENTATE DEGENERATION", "Opticocochleodentate Degeneration", "Opticocochleodentate degeneration", "Opticocochleodentate degeneration (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Opticocochleodentate degeneration", "shortest_name_length": 33}
{"curie": "MONDO:0017332", "names": ["pash syndrome", "pyoderma gangrenosum-acne-suppurative hidradenitis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyoderma gangrenosum-acne-suppurative hidradenitis syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0017561", "names": ["congenital genu flexum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital genu flexum", "shortest_name_length": 22}
{"curie": "MONDO:0009244", "names": ["FREESIA FLOWERS, INABILITY TO SMELL", "Freesia Flowers, inability to smell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Freesia Flowers, inability to smell", "shortest_name_length": 35}
{"curie": "MONDO:0009372", "names": ["Kynureninase defects", "xanthurenic aciduria", "Hydroxykynureninuria", "HYDROXYKYNURENINURIA", "Xanthurenic aciduria", "hydroxykynureninuria", "XANTHURENIC ACIDURIA", "Kynureninase deficiency", "kynureninase deficiency", "Xanthurenic aciduria (finding)", "Hydroxykynureninuria (disorder)", "kynureninase deficiency, partial", "KYNURENINASE DEFICIENCY, PARTIAL", "hydroxykynureninuria (diagnosis)", "Kynureninase deficiency (disorder)", "encephalopathy due to hydroxykynureninuria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephalopathy due to hydroxykynureninuria", "shortest_name_length": 20}
{"curie": "MONDO:0018933", "names": ["Mazabraud syndrome", "Mazabraud's syndrome", "Myxoma with fibrous dysplasia", "Fibrous dysplasia with intramuscular myxoma", "Fibrous dysplasia of bone with intramuscular myxoma", "Fibrous dysplasia of bone with intramuscular myxoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mazabraud syndrome", "shortest_name_length": 18}
{"curie": "MONDO:0002314", "names": ["Conjunctivitis chronic", "chronic conjunctivitis", "Chronic Conjunctivitis", "Chronic conjunctivitis", "chronic; conjunctivitis", "conjunctivitis; chronic", "Chronic conjunctivitis, NOS", "chronic conjunctivitis (disease)", "conjunctivitis (disease), chronic", "Chronic conjunctivitis (disorder)", "Unspecified chronic conjunctivitis", "chronic conjunctivitis (diagnosis)", "Chronic conjunctivitis, unspecified", "chronic conjunctivitis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic conjunctivitis", "shortest_name_length": 22}
{"curie": "MONDO:0005911", "names": ["Pharyngoconjunctival Fever", "Pharyngoconjunctival fever", "Human Adenovirus Infection", "PHARYNGOCONJUNCTIVAL FEVER", "pharyngoconjunctival fever", "Pharyngo-Conjunctival Fever", "pharyngo conjunctival fever", "pharyngo-conjunctival fever", "Human Adenovirus Infections", "Adenovirus Infection, Human", "Infection, Human Adenovirus", "Pharyngo Conjunctival Fever", "Fever, Pharyngo-Conjunctival", "Adenovirus Infections, Human", "Infections, Human Adenovirus", "Adenoviral pharyngoconjunctivitis", "Adenoviral pharygoconjunctival fever", "Adenoviral pharyngoconjunctival fever", "pharyngoconjunctival fever (diagnosis)", "Adenoviral pharyngoconjunctivitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pharyngoconjunctival fever", "shortest_name_length": 26}
{"curie": "MONDO:0008966", "names": ["LCS", "LCS1", "CHLS", "Chls", "aagenaes syndrome", "Aagenaes Syndrome", "Aagenaes syndrome", "AAGENAES SYNDROME", "Norwegian cholestasis", "lymphedema cholestasis syndrome", "cholestasis-lymphedema syndrome", "Cholestasis-Lymphedema Syndrome", "lymphedema-cholestasis syndrome", "Lymphedema-Cholestasis Syndrome", "Cholestasis lymphedema syndrome", "LYMPHEDEMA-CHOLESTASIS SYNDROME", "Cholestasis-lymphedema syndrome", "cholestasis lymphedema syndrome", "CHOLESTASIS-LYMPHEDEMA SYNDROME", "Cholestasis-lymphoedema syndrome", "Lymphedema-Cholestasis Syndrome 1", "Lymphedema - cholestasis syndrome", "cholestasis-edema, Norwegian type", "Cholestasis-edema syndrome, Norwegian type", "cholestasis-edema syndrome, Norwegian type", "Cholestasis-oedema syndrome, Norwegian type", "cholestasis-edema, Norwegian type (diagnosis)", "Cholestatic jaundice with hereditary lymphedema", "Cholestatic jaundice with hereditary lymphoedema", "Cholestasis-edema syndrome, Norwegian type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aagenaes syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0033544", "names": ["TOLCAS", "Tolchin-Le Caignec syndrome", "TOLCHIN-LE CAIGNEC SYNDROME", "intellectual developmental disorder With behavioral abnormalities and variable bone defects", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH BEHAVIORAL ABNORMALITIES AND VARIABLE BONE DEFECTS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tolchin-Le Caignec syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C1511194", "names": ["Bladder MALT Lymphoma", "Bladder Mucosa-Associated Lymphoid Tissue Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder Mucosa-Associated Lymphoid Tissue Lymphoma", "shortest_name_length": 21}
{"curie": "UMLS:C3658294", "names": ["Hereditary Antithrombin Deficiency", "Congenital Antithrombin III Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hereditary Antithrombin Deficiency", "shortest_name_length": 34}
{"curie": "UMLS:C0153690", "names": ["BONE METASTASIS", "bone metastasis", "Bony metastases", "Bone Metastasis", "bone metastases", "Bone Metastases", "bony metastasis", "Bony metastasis", "bony metastases", "BONE METASTASES", "Bone metastases", "Bony secondaries", "Metastasis to bone", "metastasis to bone", "Osseous metastasis", "metastases to bone", "osseous metastasis", "Metastases to bone", "metastatic bone tumor", "secondary bone cancer", "Bone cancer metastatic", "metastatic bone cancer", "metastatic bone tumour", "BONE NEOPLASM SECONDARY", "Metastases to bone, NOS", "Tumor metastatic to bone", "Metastatic tumor of bone", "Secondary cancer of bone", "Cancer metastatic to bone", "Metastatic tumour of bone", "Tumour metastatic to bone", "metastatic cancer to bone", "cancer metastatic to bone", "bone, metastatic cancer to", "Osteolytic bone metastases", "cancer, metastatic to bone", "Metastatic Tumor to the Bone", "Secondary malignancy of bone", "Metastatic Cancer to the Bone", "Metastatic Neoplasm to the Bone", "secondary malignant neoplasm bone", "secondary malignant neoplasm of bone", "Secondary malignant neoplasm of bone", "Metastatic malignant neoplasm to bone", "Metastatic malignant neoplasm of bone", "metastasis of malignant neoplasm to bone", "Metastatic Malignant Neoplasm to the Bone", "Secondary malignant neoplasm of bone, NOS", "Metastatic Malignant Neoplasm in the Bone", "Metastatic malignant neoplasm to bone, NOS", "secondary malignant neoplasm of bone (diagnosis)", "Metastatic malignant neoplasm to bone (disorder)", "Secondary malignant neoplasm of bone and bone marrow", "metastasis of malignant neoplasm to bone (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to bone", "shortest_name_length": 15}
{"curie": "UMLS:C1297883", "names": ["Radial scar", "radial scar", "Radial Scar", "radial scars", "radial scarring", "Radial Sclerosing Lesion", "Complex Sclerosing Lesion", "Radial Scar/Complex Sclerosing Lesion", "Radial scar (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radial scar", "shortest_name_length": 11}
{"curie": "MONDO:0001516", "names": ["SMA", "Spinal Amyotrophy", "spinal amyotrophy", "Spinal amyotrophy", "Amyotrophy, Spinal", "Spinal Amyotrophies", "SPINE MUSCLE ATROPHY", "Amyotrophies, Spinal", "SPINAL MUSCLE ATROPHY", "spinal muscle atrophy", "muscle spinal atrophy", "Spinal muscle wasting", "muscular atrophy spinal", "atrophy spinal muscular", "muscular spinal atrophy", "atrophy muscular spinal", "Spinal Muscular Atrophy", "spinal muscular atrophy", "Spinal muscular atrophy", "Muscular Atrophy, Spinal", "Atrophy, Spinal Muscular", "MUSCULAR ATROPHY, SPINAL", "atrophies muscular spinal", "Spinal muscle degeneration", "atrophy muscular sma spinal", "Spinal muscular atrophy, NOS", "SMA - Spinal muscular atrophy", "inherited spinal muscular atrophy", "muscular atrophy inherited spinal", "Spinal muscular atrophy (disorder)", "spinal muscular atrophy (diagnosis)", "Spinal muscular atrophy, unspecified", "inherited spinal muscular atrophy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal muscular atrophy", "shortest_name_length": 3}
{"curie": "MONDO:0001291", "names": ["brain compression", "Brain compression", "brain; compression", "compression; brain", "Compression, brain", "compression of brain", "Compression of brain", "Compression of brain, NOS", "Compression of brain (disorder)", "compression of brain (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brain compression", "shortest_name_length": 17}
{"curie": "MONDO:0016101", "names": ["marek disease", "Marek disease", "Marek Disease", "fowl paralyses", "Fowl Paralyses", "Fowl Paralysis", "Mareks Disease", "fowl paralysis", "Marek's disease", "marek's disease", "Paralysis, Fowl", "Marek's Disease", "Paralyses, Fowl", "Neurolymphomatoses", "neurolymphomatosis", "Neurolymphomatosis", "Marek's disease (disorder)", "Neurolymphomatosis gallinarum", "Neurolymphomatosis (disorder)", "Neurolymphomatosis (diagnosis)", "paraneoplastic neuropathy peripheral neurolymphomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurolymphomatosis", "shortest_name_length": 13}
{"curie": "UMLS:C0085592", "names": ["heat cramp", "HEAT CRAMP", "Heat cramp", "Heat Cramp", "heat cramps", "Heat cramps", "Heat Cramps", "Stokers' cramp", "cramp(s); heat", "heat; cramp(s)", "stoker's; cramp(s)", "cramp(s); stoker's", "Heat cramp (finding)", "Effects of heat cramp", "heat cramps (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Heat Cramps", "shortest_name_length": 10}
{"curie": "MONDO:0012563", "names": ["HPE9", "Holoprosencephaly 9", "HOLOPROSENCEPHALY 9", "holoprosencephaly 9", "GLI2 holoprosencephaly", "holoprosencephaly type 9", "holoprosencephaly caused by mutation in GLI2", "Pituitary Anomalies with Holoprosencephaly-Like Features", "PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES", "pituitary anomalies with holoprosencephaly-like features", "PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES (disorder)", "holoprosencephaly with microphthalmia and first branchial Arch anomalies", "holoprosencephaly with microphthalmia and first branchial arch anomalies", "HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "holoprosencephaly 9", "shortest_name_length": 4}
{"curie": "OMIM:614374", "names": [], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"]}
{"curie": "MONDO:0018848", "names": ["Ormond disease", "ormond disease", "Ormond Disease", "ORMOND DISEASE", "Disease, Ormond", "disease ormonds", "Ormond's disease", "ormond's disease", "Ormond's Disease", "Disease, Ormond's", "Retroperitoneal fibrosis", "retroperitoneal fibroses", "FIBROSIS RETROPERITONEAL", "Retroperitoneal Fibroses", "Fibrosis retroperitoneal", "retroperitoneal fibrosis", "Retroperitoneal Fibrosis", "fibrosis retroperitoneal", "RETROPERITONEAL FIBROSIS", "Fibroses, Retroperitoneal", "Fibrosis, Retroperitoneal", "fibrosis; retroperitoneal", "infection; ormond's disease", "Sclerosing retroperitonitis", "ormond's disease; infection", "RPF - Retroperitoneal fibrosis", "Idiopathic retroperitoneal fibrosis", "idiopathic retroperitoneal fibrosis", "Retroperitoneal fibrosis (disorder)", "Idiopathic Retroperitoneal Fibrosis", "RETROPERITONEAL FIBROSIS IDIOPATHIC", "retroperitoneal fibrosis (diagnosis)", "IgG4-related retroperitoneal fibrosis", "FIBROSIS, RETROPERITONEAL, IDIOPATHIC", "retroperitoneal; fibrosis, idiopathic", "Idiopathic retroperitoneal fibrosis (disorder)", "idiopathic retroperitoneal fibrosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IgG4-related retroperitoneal fibrosis", "shortest_name_length": 14}
{"curie": "MONDO:0009384", "names": ["Leydig cell agenesis", "LEYDIG CELL AGENESIS", "Leydig Cell Agenesis", "Leydig cell hypoplasia", "Leydig cell dysgenesis", "LHCGR Leydig cell hypoplasia", "Leydig cell Hypoplasia, type 2", "Leydig cell hypoplasia, type I", "Leydig cell hypoplasia, type 1", "LEYDIG CELL HYPOPLASIA, TYPE I", "Leydig Cell Hypoplasia, Type I", "Leydig cell agenesis (disorder)", "Leydig Cell Hypoplasia, Partial", "LEYDIG CELL HYPOPLASIA, PARTIAL", "Leydig Cell Hypoplasia, Type II", "LEYDIG CELL HYPOPLASIA, TYPE II", "Leydig cell hypoplasia, partial", "Leydig cell hypoplasia, complete", "Leydig Cell Hypoplasia, Complete", "Leydig cell agenesis (diagnosis)", "LEYDIG CELL HYPOPLASIA, COMPLETE", "Luteinizing Hormone Resistance, Female", "LUTEINIZING HORMONE RESISTANCE, FEMALE", "luteinizing hormone resistance, female", "Gonadotropin unresponsiveness syndrome", "Gonadotrophin unresponsiveness syndrome", "leydig cell hypoplasia with pseudohermaphroditism", "Leydig cell hypoplasia caused by mutation in LHCGR", "Leydig Cell Hypoplasia with Male Pseudohermaphroditism", "Leydig cell hypoplasia with male pseudohermaphroditism", "LEYDIG CELL HYPOPLASIA WITH MALE PSEUDOHERMAPHRODITISM", "Male Hypergonadotropic Hypogonadism Due To LHCGR Defect", "hypergonadotropic hypogonadism, Male, due to Lhcgr defect", "HYPERGONADOTROPIC HYPOGONADISM, MALE, DUE TO LHCGR DEFECT", "Hypergonadotropic Hypogonadism, Male, Due To LHCGR Defect", "leydig cell hypoplasia with hypergonadotropic hypogonadism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leydig cell hypoplasia, type 1", "shortest_name_length": 20}
{"curie": "MONDO:0017149", "names": ["Drug- or toxin-induced PAH", "drug- or toxin-induced PAH", "pulmonary hypertension drug-induced", "Drug-induced pulmonary hypertension", "Pulmonary hypertension caused by drug", "Pulmonary arterial hypertension caused by drug", "Drug-induced pulmonary hypertension (diagnosis)", "Pulmonary arterial hypertension induced by drug", "Pulmonary hypertension caused by drug (disorder)", "Drug- or toxin-induced pulmonary arterial hypertension", "drug- or toxin-induced pulmonary arterial hypertension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "drug- or toxin-induced pulmonary arterial hypertension", "shortest_name_length": 26}
{"curie": "MONDO:0011879", "names": ["HMN7B", "HMN 7B", "DHMN7B", "Dhmn7B", "HMN VIIB", "Harper-Young myopathy", "LOWER MOTOR NEURON DISEASE, DYNACTIN TYPE", "Lower motor neuron disease, dynactin type", "Lower Motor Neuron Disease, Dynactin Type", "DCTN1 neuronopathy, distal hereditary motor", "distal hereditary motor neuronopathy type 7B", "neuropathy, distal hereditary motor, type 7B", "distal hereditary motor neuropathy type VIIB", "neuronopathy, distal hereditary motor, type 7B", "NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB", "Neuropathy, Distal Hereditary Motor, Type VIIB", "NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB", "Neuronopathy, Distal Hereditary Motor, Type Viib", "neuronopathy, distal hereditary motor, type VIIB", "distal spinal muscular atrophy with vocal cord paralysis type 7B", "neuronopathy, distal hereditary motor caused by mutation in DCTN1", "neuropathy, distal hereditary motor, with vocal cord paralysis, type 7B", "Neuropathy, Distal Hereditary Motor, With Vocal Cord Paralysis, Type VIIB", "NEUROPATHY, DISTAL HEREDITARY MOTOR, WITH VOCAL CORD PARALYSIS, TYPE VIIB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuronopathy, distal hereditary motor, type 7B", "shortest_name_length": 5}
{"curie": "UMLS:C1096034", "names": ["Infusion site induration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infusion site induration", "shortest_name_length": 24}
{"curie": "MONDO:0032796", "names": ["HIES4", "HIES4B", "hyper IgE recurrent infection syndrome 4", "HYPER-IgE RECURRENT INFECTION SYNDROME 4, AUTOSOMAL RECESSIVE", "hyper-IgE recurrent infection syndrome 4, autosomal recessive", "HYPER-IgE RECURRENT INFECTION SYNDROME 4B, AUTOSOMAL RECESSIVE", "hyper-IgE recurrent infection syndrome 4B, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyper-IgE recurrent infection syndrome 4, autosomal recessive", "shortest_name_length": 5}
{"curie": "UMLS:C5420819", "names": ["Iris Mixed Cell Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Iris Mixed Cell Melanoma", "shortest_name_length": 24}
{"curie": "UMLS:C0311370", "names": ["Lupus anticoagulant", "SLE inhibitor syndrome", "lupus anticoagulant disorder", "Lupus Anticoagulant Disorder", "Lupus anticoagulant syndrome", "lupus anticoagulant syndrome", "Lupus anticoagulant disorder", "LUPUS ANTICOAGULANT SYNDROME", "Lupus anticoagulant inhibitor syndrome", "Lupus anticoagulant disorder (disorder)", "lupus anticoagulant syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lupus anticoagulant disorder", "shortest_name_length": 19}
{"curie": "MONDO:0019250", "names": ["disorder of biogenic amine metabolism and transport", "inborn disorder of biogenic amine metabolism and transport"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of biogenic amine metabolism and transport", "shortest_name_length": 51}
{"curie": "MONDO:0005339", "names": ["MPB", "Common baldness", "Frontal balding", "Pattern baldness", "pattern baldness", "Androgenic alopecia", "androgenic alopecia", "Hereditary alopecia", "alopecia androgenic", "Male Pattern Baldness", "Male-pattern baldness", "male-pattern baldness", "Male pattern alopecia", "Male pattern baldness", "Male Pattern Alopecia", "alopecia androgenetic", "male pattern baldness", "male pattern alopecia", "Androgenetic alopecia", "baldness male pattern", "androgenetic alopecia", "baldness; male-pattern", "BALDNESS, MALE PATTERN", "Baldness, Male Pattern", "Alopecia, Male Pattern", "frontal male pattern baldness", "Male pattern alopecia (disorder)", "Frontal balding (male pattern baldness)", "male pattern baldness (physical finding)", "alopecia androgenetica, male pattern baldness", "frontal male pattern baldness (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "androgenetic alopecia", "shortest_name_length": 3}
{"curie": "UMLS:C0006274", "names": ["viral bronchiolitis", "Viral Bronchiolitis", "Bronchiolitis, Viral", "Viral Bronchiolitides", "Bronchiolitides, Viral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bronchiolitis, Viral", "shortest_name_length": 19}
{"curie": "UMLS:C3711543", "names": ["Xlcsnb", "X-Linked Csnb"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-Linked Csnb", "shortest_name_length": 6}
{"curie": "MONDO:0000775", "names": ["Drug allergy", "DRUG ALLERGY", "Drug Allergy", "allergy drug", "drug allergy", "Allergy, Drug", "drug; allergy", "allergy drugs", "Drug Allergies", "Drug allergies", "allergies drug", "drug allergies", "allergies drugs", "Allergies, Drug", "Allergy to drug", "Allergy to drugs", "Medicine allergy", "Drug allergy NOS", "Drug allergy, NOS", "Medication allergy", "allergy medication", "medication allergy", "allergy medications", "allergies medication", "Drug Hypersensitivity", "Drug hypersensitivity", "allergies medications", "drug hypersensitivity", "drugs hypersensitivity", "drug allergic reaction", "Hypersensitivity, Drug", "Allergic drug reaction", "allergic drug reaction", "hypersensitivity; drug", "drug; hypersensitivity", "allergic reaction drug", "Drug reaction, allergic", "allergic drugs reaction", "allergic drug reactions", "Drug Hypersensitivities", "drugs allergic reaction", "Hypersensitivities, Drug", "drug allergy (diagnosis)", "allergic drugs reactions", "IgE-mediated drug allergy", "allergic reaction to drug", "Allergy to drug (finding)", "Allergic reaction to drug", "Drug hypersensitivity NOS", "Allergic reaction;drug(s)", "allergy of exposure to drug", "Allergic reaction to medication", "Allergic reaction caused by drug", "exposure to drug allergic disease", "allergic drug reaction (diagnosis)", "Immunoglobulin E-mediated drug allergy", "Allergic reaction caused by drug (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "drug allergy", "shortest_name_length": 12}
{"curie": "UMLS:C0278811", "names": ["unresectable extrahepatic bile duct cancer", "Unresectable Extrahepatic Bile Duct Cancer", "extrahepatic bile duct cancer, unresectable", "bile duct cancer, unresectable extrahepatic", "Unresectable Extrahepatic Bile Duct Carcinoma", "Unresectable Cancer of Extrahepatic Bile Duct", "Non-Resectable Extrahepatic Bile Duct Carcinoma", "Unresectable Cancer of the Extrahepatic Bile Duct", "Unresectable Extrahepatic (Distal) Bile Duct Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Extrahepatic Bile Duct Carcinoma", "shortest_name_length": 42}
{"curie": "UMLS:C5556686", "names": ["Minor Salivary Gland Intraductal Papillary Neoplasm", "Minor Salivary Gland Intraductal Papillary-Cystic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Minor Salivary Gland Intraductal Papillary Neoplasm", "shortest_name_length": 51}
{"curie": "MONDO:0015351", "names": ["Neuropathy with hearing impairment", "neuropathy with hearing impairment", "Peripheral neuropathy with sensorineural hearing impairment syndrome", "Peripheral neuropathy with sensorineural hearing impairment syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuropathy with hearing impairment", "shortest_name_length": 34}
{"curie": "MONDO:0008056", "names": ["DM", "MD1", "DM1", "STEINERT DISEASE", "Steinert disease", "Steinert Disease", "Steinert Syndrome", "Steinert syndrome", "Steinert's disease", "Myotonic Dystrophy 1", "dystrophia myotonica", "Dystrophia myotonica", "DYSTROPHIA MYOTONICA", "MYOTONIC DYSTROPHY 1", "myotonic dystrophy 1", "Dystrophia Myotonica 1", "DYSTROPHIA MYOTONICA 1", "dystrophia myotonica 1", "DMPK myotonic dystrophy", "myotonic dystrophy type 1", "Myotonic dystrophy type 1", "dystrophia myotonica type 1", "Steinert myotonic dystrophy", "congenital myotonic dystrophy", "myotonic dystrophy of Steinert", "myotonic dystrophy, type 1 (DM1)", "Steinert Myotonic Dystrophy Syndrome", "Steinert myotonic dystrophy syndrome", "myotonic dystrophy, type 1 (DM1) (diagnosis)", "myotonic dystrophy caused by mutation in DMPK", "Steinert myotonic dystrophy syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myotonic dystrophy type 1", "shortest_name_length": 2}
{"curie": "UMLS:C1335118", "names": ["Mouth Granular Cell Tumor", "Granular Cell Tumor of Mouth", "Mouth Granular Cell Neoplasm", "Oral Cavity Granular Cell Tumor", "Granular Cell Neoplasm of Mouth", "Granular Cell Tumor of the Mouth", "Oral Cavity Granular Cell Neoplasm", "Granular Cell Tumor of Oral Cavity", "Granular Cell Neoplasm of the Mouth", "Granular Cell Neoplasm of Oral Cavity", "Granular Cell Tumor of the Oral Cavity", "Granular Cell Neoplasm of the Oral Cavity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral Cavity Granular Cell Tumor", "shortest_name_length": 25}
{"curie": "MONDO:0035944", "names": ["Hypodiploid ALL", "B-ALL with hypodiploidy", "B Lymphoblastic Leukemia/Lymphoma with Hypodiploidy", "B-Lymphoblastic Leukemia/Lymphoma with Hypodiploidy", "B lymphoblastic leukemia lymphoma with hypodiploidy", "B-lymphoblastic leukemia/lymphoma with hypodiploidy", "B lymphoblastic leukaemia lymphoma with hypodiploidy", "B lymphoblastic leukemia lymphoma with hypodiploidy (disorder)", "B lymphoblastic leukemia lymphoma with hypodiploidy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-lymphoblastic leukemia/lymphoma with hypodiploidy", "shortest_name_length": 15}
{"curie": "UMLS:C4321358", "names": ["IMC", "Immune-Mediated Coagulopathy", "Immune-Mediated Coagulation Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immune-Mediated Coagulopathy", "shortest_name_length": 3}
{"curie": "MONDO:0015263", "names": ["SUNDS", "Bangungut", "dream disease", "Dream disease", "brugada syndrome", "Brugada Syndrome", "Brugada syndrome", "brugadas syndrome", "Brugada ECG Pattern", "ECG Pattern, Brugada", "Pokkuri death syndrome", "Brugada Type ECG Pattern", "Brugada Syndrome (disorder)", "Brugada syndrome (disorder)", "Brugada syndrome (diagnosis)", "Sudden Unexplained Death Syndrome", "sudden unexpected nocturnal death syndrome", "Sudden Unexplained Nocturnal Death Syndrome", "SUDDEN UNEXPLAINED NOCTURNAL DEATH SYNDROME", "sudden unexplained nocturnal death syndrome", "Brugada type idiopathic ventricular fibrillation", "Idiopathic ventricular fibrillation, Brugada type", "idiopathic ventricular fibrillation, Brugada type", "Sudden Unexplained Nocturnal Death Syndrome (SUNDS)", "RIGHT BUNDLE BRANCH BLOCK, ST SEGMENT ELEVATION, AND SUDDEN DEATH SYNDROME", "Right Bundle Branch Block, ST Segment Elevation, and Sudden Death Syndrome", "right bundle branch block, ST segment elevation, and sudden death syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brugada syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0393734", "names": ["Psychomotor status", "epilepsy; status, complex partial", "Complex partial status epilepticus", "Complex Partial Status Epilepticus", "Status Epilepticus, Complex Partial", "status; epilepticus, complex partial", "Complex partial status epilepticus (disorder)", "Complex partial status epilepticus (diagnosis)", "seizure disorder complex partial status epilepticus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Complex Partial Status Epilepticus", "shortest_name_length": 18}
{"curie": "UMLS:C4553781", "names": ["Stage 0a Renal Pelvis and Ureter Cancer", "stage 0a renal pelvis and ureter cancer AJCC v8", "Stage 0a Renal Pelvis and Ureter Cancer AJCC v8", "stage 0a renal pelvis and ureter urothelial carcinoma AJCC v8", "Stage 0a Renal Pelvis and Ureter Urothelial Carcinoma AJCC v8", "stage 0a transitional cell cancer of the renal pelvis and ureter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0a Renal Pelvis and Ureter Cancer AJCC v8", "shortest_name_length": 39}
{"curie": "MONDO:0014173", "names": ["MCPH11", "primary autosomal recessive microcephaly 11", "microcephaly 11, primary, autosomal recessive", "MICROCEPHALY 11, PRIMARY, AUTOSOMAL RECESSIVE", "PHC1 autosomal recessive primary microcephaly", "autosomal recessive primary microcephaly caused by mutation in PHC1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly 11, primary, autosomal recessive", "shortest_name_length": 6}
{"curie": "MONDO:0018883", "names": ["GCL", "BSCL", "Brunzell syndrome", "total lipodystrophy", "Total Lipodystrophy", "lipoatrophic diabetes", "Lawrence-Seip Syndrome", "Lawrence-Seip syndrome", "Beradinelli-Seip syndrome", "Berardinelli Seip syndrome", "Berardinelli Seip Syndrome", "Seip-Bernardinelli Syndrome", "Seip-Bernardinelli syndrome", "Berardinelli Lipodystrophy Syndrome", "Berardinelli lipodystrophy syndrome", "Congenital Generalized Lipodystrophy", "congenital generalized lipodystrophy", "generalized congenital lipodystrophy", "Berardinelli-Seip Congenital Lipodystrophy", "Berardinelli-Seip congenital lipodystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Berardinelli-Seip congenital lipodystrophy", "shortest_name_length": 3}
{"curie": "MONDO:0004307", "names": ["Meninges Sarcomatosis", "meninges sarcomatosis", "meningeal sarcomatosis", "Meningeal Sarcomatosis", "Meningeal sarcomatosis", "sarcomatosis of meninges", "Sarcomatosis of Meninges", "Sarcomatosis of the Meninges", "sarcomatosis of the meninges", "meningeal cluster sarcomatosis", "Meningeal sarcomatosis (morphologic abnormality)", "meningeal sarcomatosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sarcomatosis of the meninges", "shortest_name_length": 21}
{"curie": "MONDO:0005155", "names": ["CIRRHOSIS", "Cirrhosis", "cirrhosis", "Liver Cirrhosis", "LIVER CIRRHOSIS", "liver cirrhosis", "CIRRHOSIS LIVER", "Cirrhosis liver", "Liver cirrhosis", "liver; cirrhosis", "cirrhosis; liver", "Cirrhosis, Liver", "Liver--Cirrhosis", "HEPATIC CIRRHOSIS", "Cirrhosis (Liver)", "Hepatic cirrhosis", "Hepatic Cirrhosis", "hepatic cirrhosis", "CIRRHOSIS OF LIVER", "cirrhosis of liver", "Cirrhosis of liver", "Cirrhosis, Hepatic", "Cirrhosis (of);liver", "Hepatic cirrhosis NOS", "Hepatic cirrhosis, NOS", "cirrhosis of the liver", "Cirrhosis of the Liver", "CL - Cirrhosis of liver", "Cirrhosis of liver, NOS", "Cirrhosis (of liver) NOS", "Cirrhosis of liver (disorder)", "hepatic cirrhosis (diagnosis)", "Scar tissue replaces healthy tissue in the liver"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cirrhosis of liver", "shortest_name_length": 9}
{"curie": "MONDO:0003007", "names": ["Renal Cell Cancer", "renal cell cancer", "childhood renal cell carcinoma", "pediatric renal cell carcinoma", "Pediatric Renal Cell Carcinoma", "Childhood Renal Cell Carcinoma", "Pediatric Kidney Cell Carcinoma", "Childhood Kidney Cell Carcinoma", "pediatric kidney cell carcinoma", "childhood kidney cell carcinoma", "pediatric renal cell carcinoma (disease)", "childhood renal cell carcinoma (disease)", "renal cell carcinoma (disease) of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood kidney cell carcinoma", "shortest_name_length": 17}
{"curie": "UMLS:C1868795", "names": ["Vasoplegia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vasoplegia syndrome", "shortest_name_length": 19}
{"curie": "UMLS:C0279632", "names": ["M7 Adult Acute Leukemia", "Adult Acute M7 Leukemia", "Acute Megakaryoblastic Leukemia", "Adult Acute Megakaryocytic Leukemia", "leukemia, adult acute megakaryocytic", "megakaryocytic leukemia, adult acute", "acute megakaryocytic leukemia, adult", "Adult Acute Megakaryoblastic Leukemia", "M7 Adult Acute Megakaryocytic Leukemia", "M7 adult acute megakaryocytic leukemia", "Adult Acute Megakaryocytic Leukemia (M7)", "adult acute megakaryoblastic leukemia (M7)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Acute Megakaryoblastic Leukemia", "shortest_name_length": 23}
{"curie": "MONDO:0014452", "names": ["Dysfibrinogenemia", "dysfibrinogenemia", "dysfibrinogenaemia", "dysfibrinogenemias", "Dysfibrinogenaemia", "hypodysfibrinogenemia", "Dysfibrinogenemia, NOS", "familial dysfibrinogenemia", "dysfibrinogenemia, familial", "Dysfibrinogenemia (disorder)", "Congenital dysfibrinogenemia", "congenital dysfibrinogenemia", "CONGENITAL DYSFIBRINOGENEMIA", "Hereditary dysfibrinogenemia", "dysfibrinogenemia, congenital", "DYSFIBRINOGENEMIA, CONGENITAL", "Hereditary dysfibrinogenaemia", "Congenital dysfibrinogenaemia", "Dysfibrinogenemia, Congenital", "Dysfibrinogenemia (congenital)", "Congenital dysfibrinogenemia, NOS", "hypodysfibrinogenemia, congenital", "Hypodysfibrinogenemia, Congenital", "HYPODYSFIBRINOGENEMIA, CONGENITAL", "Hereditary dysfibrinogenemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial dysfibrinogenemia", "shortest_name_length": 17}
{"curie": "UMLS:C0017128", "names": ["Stomach Fistula", "stomach fistula", "fistula gastric", "Gastric Fistula", "fistula stomach", "Gastric fistula", "gastric fistula", "stomach; fistula", "fistula; stomach", "fistulas gastric", "Fistula, Stomach", "Fistula, Gastric", "Fistula of stomach", "fistula of stomach", "GF - Gastric fistula", "Gastric fistula (disorder)", "gastric fistula (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Fistula", "shortest_name_length": 15}
{"curie": "MONDO:0016450", "names": ["cAHA", "cAIHA", "cold AIHA", "autoimmune hemolytic anemia, cold type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune hemolytic anemia, cold type", "shortest_name_length": 4}
{"curie": "MONDO:0032903", "names": ["AMC4", "AMCNACC", "Zain Syndrome", "ZAIN SYNDROME", "Zain syndrome", "arthrogryposis multiplex congenita-4", "ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC, WITH AGENESIS OF THE CORPUS CALLOSUM", "arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum", "arthrogryposis multiplex congenita 4, neurogenic, with agenesis of the corpus callosum", "ARTHROGRYPOSIS MULTIPLEX CONGENITA 4, NEUROGENIC, WITH AGENESIS OF THE CORPUS CALLOSUM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis multiplex congenita 4, neurogenic, with agenesis of the corpus callosum", "shortest_name_length": 4}
{"curie": "MONDO:0006489", "names": ["vagina melanoma", "vaginal melanoma", "Vaginal Melanoma", "melanoma of vagina", "Melanoma of Vagina", "Melanoma of the Vagina", "melanoma of the vagina", "vagina melanoma (disease)", "melanoma (disease) of vagina", "mucosal melanoma of the vulva/vagina"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vaginal melanoma", "shortest_name_length": 15}
{"curie": "MONDO:0018625", "names": ["classic SPS", "classic stiff person syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "classic stiff person syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0010803", "names": ["EKNS", "EIKEN SYNDROME", "Eiken syndrome", "Eiken skeletal dysplasia", "EIKEN SKELETAL DYSPLASIA", "Eiken Skeletal Dysplasia", "Eiken syndrome (disorder)", "Bone Modeling Defect of Hands and Feet", "bone modeling defect of hands and feet", "BONE MODELING DEFECT OF HANDS AND FEET"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eiken syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C5557567", "names": ["Metastatic HER2 Low Breast Carcinoma", "Metastatic HER2-Low Breast Carcinoma", "Metastatic HER2-Low Breast Adenocarcinoma", "Metastatic HER2 Low Breast Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic HER2-Low Breast Carcinoma", "shortest_name_length": 36}
{"curie": "UMLS:C0854326", "names": ["Escherichia", "Escherichia infection", "Escherichia infections", "infection; Escherichia", "Escherichia; infection", "Escherichia infection NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Escherichia infection", "shortest_name_length": 11}
{"curie": "UMLS:C1519854", "names": ["Uterine Corpus Leiomyoma, Mitotically Active Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Corpus Leiomyoma, Mitotically Active Variant", "shortest_name_length": 52}
{"curie": "OMIM:111740", "names": [], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"]}
{"curie": "MONDO:0011312", "names": ["TCO", "TCO1", "TCO 1", "thyroid carcinoma, nonmedullary, with cell oxyphilia", "Nonmedullary thyroid carcinoma, with or without cell oxyphilia", "nonmedullary thyroid carcinoma, with or without cell oxyphilia", "THYROID CARCINOMA, NONMEDULLARY, WITH OR WITHOUT CELL OXYPHILIA", "thyroid carcinoma, nonmedullary, with or without cell oxyphilia", "Thyroid Carcinoma, Nonmedullary, With Or Without Cell Oxyphilia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid carcinoma, nonmedullary, with or without cell oxyphilia", "shortest_name_length": 3}
{"curie": "MONDO:0013976", "names": ["ECTD9", "ectodermal dysplasia 9", "ectodermal dysplasia 9, hair/nail type", "ECTODERMAL DYSPLASIA 9, HAIR/NAIL TYPE", "HOXC13 pure hair and nail ectodermal dysplasia", "pure hair and nail ectodermal dysplasia caused by mutation in HOXC13"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia 9, hair/nail type", "shortest_name_length": 5}
{"curie": "UMLS:C3275114", "names": ["Moderate Cardiac Valve Stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Moderate Cardiac Valve Stenosis", "shortest_name_length": 31}
{"curie": "UMLS:C0342199", "names": ["Iodine deficiency syndrome", "syndrome; iodine-deficiency", "Iodine deficiency syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Iodine deficiency syndrome", "shortest_name_length": 26}
{"curie": "UMLS:C5400989", "names": ["Zoonotic Spillover", "Zoonotic Spillovers", "Spillovers, Zoonotic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Zoonotic Spillover", "shortest_name_length": 18}
{"curie": "MONDO:0007758", "names": ["EPPK", "Ppke", "callus", "Tyloma", "Callus", "CALLUS", "tyloma", "Tylosis", "tylomas", "callous", "tylosis", "keratoma", "callused", "Keratoma", "Calluses", "keratosis", "Callosity", "callosity", "Keratosis", "keratomas", "Keratomas", "Callosities", "callosities", "Skin callus", "skin callus", "hyperkeratoses", "Hyperkeratosis", "HYPERKERATOSIS", "hyperkeratosis", "Hyperkeratoses", "HYPERKERATOSES", "Unna-Thost disease", "Unna-Thost Disease", "Greither Keratosis", "callus (diagnosis)", "skin hyperkeratosis", "Hyperkeratosis, NOS", "HK - Hyperkeratosis", "Unna-Thost Syndrome", "Callosity (disorder)", "Hyperkeratotic callus", "KERATOSIS OF GREITHER", "Keratosis of Greither", "keratosis of Greither", "hyperkeratosis of skin", "Thost-Unna keratoderma", "Excessive cornification", "Increased Keratinization", "Thickened stratum corneum", "hyperkeratosis (diagnosis)", "Hyperkeratosis of skin, NOS", "skin texture hyperkeratosis", "Thickening of stratum corneum", "hyperkeratosis (physical finding)", "Palmoplantar Keratoderma, Vorner Type", "palmoplantar keratoderma, Vorner type", "PALMOPLANTAR KERATODERMA, VORNER TYPE", "Epidermolytic Palmoplantar Keratoderma", "epidermolytic palmoplantar keratoderma", "keratoderma, epidermolytic palmoplantar", "hyperkeratosis, localized epidermolytic", "palmoplantar keratoderma, epidermolytic", "Hyperkeratosis (morphologic abnormality)", "Keratosis Palmaris et Plantaris Familiaris", "KERATOSIS PALMARIS ET PLANTARIS FAMILIARIS", "keratosis palmaris Et plantaris Familiaris", "Thost-Unna diffuse palmoplantar keratoderma", "Excessive growth of horny tissue of the skin", "Diffuse palmoplantar keratoderma of Thost-Unna", "epidermolytic palmoplantar keratoderma of Vörner", "epidermolytic palmoplantar keratoderma of Voerner", "epidermolytic palmoplantar keratoderma of VC6rner", "hyperkeratosis palmoplantar localized epidermolytic", "Diffuse palmoplantar keratoderma of Thost-Unna (disorder)", "PALMOPLANTAR KERATODERMA, EPIDERMOLYTIC, WITH KNUCKLE PADS", "Palmoplantar Keratoderma, Epidermolytic, with Knuckle Pads", "palmoplantar keratoderma, epidermolytic, with knuckle pads", "diffuse erythrodermic palmoplantar keratoderma, Vörner type", "diffuse erythrodermic palmoplantar keratoderma, Voerner type", "diffuse erythrodermic palmoplantar keratoderma, VC6rner type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolytic palmoplantar keratoderma", "shortest_name_length": 4}
{"curie": "MONDO:0011166", "names": ["Irons Bhan syndrome", "Irons-Bhan syndrome", "IRONS-BIANCHI SYNDROME", "Irons-Bianchi Syndrome", "Irons Bianchi syndrome", "Irons-Bianchi syndrome", "lymphedema-atrial septal defects-facial changes syndrome", "Lymphedema-atrial septal defects-facial changes syndrome", "Lymphedema, atrial septal defect, facial changes syndrome", "Lymphoedema, atrial septal defect, facial changes syndrome", "LYMPHEDEMA, ATRIAL SEPTAL DEFECT, AND CHARACTERISTIC FACIES", "Lymphedema, Atrial Septal Defect, And Characteristic Facies", "lymphedema, atrial septal defect, and characteristic facies", "lymphedema, CARDIAC septal defects, and characteristic facies", "Lymphedema, Cardiac Septal Defects, And Characteristic Facies", "LYMPHEDEMA, CARDIAC SEPTAL DEFECTS, AND CHARACTERISTIC FACIES", "lymphedema, atrial septal defect, and characteristic facial changes", "Lymphedema, atrial septal defect, and characteristic facial changes", "Lymphedema, atrial septal defect, facial changes syndrome (disorder)", "Autosomal recessive syndrome of lymphedema, hydroceles, atrial septal defect, and characteristic facial changes", "autosomal recessive syndrome of lymphedema, hydroceles, atrial septal defect, and characteristic facial changes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphedema-atrial septal defects-facial changes syndrome", "shortest_name_length": 19}
{"curie": "UMLS:C4054534", "names": ["Meningioangiomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meningioangiomatosis", "shortest_name_length": 20}
{"curie": "MONDO:0016510", "names": ["epibulbar lipodermoid-preauricular appendage-polythelia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epibulbar lipodermoid-preauricular appendage-polythelia syndrome", "shortest_name_length": 64}
{"curie": "UMLS:C2936170", "names": ["Patent Ductus Arteriosus Familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Patent Ductus Arteriosus Familial", "shortest_name_length": 33}
{"curie": "UMLS:C0677660", "names": ["Emotional problem", "Emotional Problem", "emotional problems", "Emotional problems", "EMOTIONAL PROBLEMS", "disturbed emotionally", "Emotionally disturbed", "emotionally disturbed", "Emotionally Disturbed", "Emotional problems (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Emotional problems", "shortest_name_length": 17}
{"curie": "UMLS:C3874401", "names": ["Intestinal hemorrhage due to angiodysplasia of intestine", "Intestinal haemorrhage due to angiodysplasia of intestine", "Intestinal hemorrhage due to angiodysplasia of intestine (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal hemorrhage due to angiodysplasia of intestine", "shortest_name_length": 56}
{"curie": "MONDO:0009705", "names": ["hepatic CPT1", "CPT1A deficiency", "CPT I Deficiency", "CPT I deficiency", "CPT I DEFICIENCY", "CPT 1 deficiency", "CPT 1A Deficiency", "L-CPT1 deficiency", "L-CPTI deficiency", "L-CPT 1 deficiency", "hepatic CPT deficiency type I", "CPT Deficiency, Hepatic, Type I", "CPT DEFICIENCY, HEPATIC, TYPE I", "CPT deficiency, hepatic, type 1", "cpt deficiency, hepatic, type IA", "Carnitine Palmitoyltransferase 1 deficiency", "Carnitine palmitoyltransferase 1 deficiency", "Carnitine palmitoyltransferase I deficiency", "carnitine palmitoyltransferase I deficiency", "Carnitine Palmitoyltransferase I Deficiency", "carnitine palmitoyltransferase deficiency 1", "CARNITINE PALMITOYLTRANSFERASE I DEFICIENCY", "Carnitine palmitoyl transferase 1 deficiency", "Carnitine Palmitoyltransferase IA Deficiency", "Carnitine palmitoyltransferase 1A deficiency", "CARNITINE PALMITOYLTRANSFERASE IA DEFICIENCY", "Carnitine Palmitoyltransferase 1A deficiency", "carnitine palmitoyl transferase 1A deficiency", "Carnitine palmitoyl transferase 1A deficiency", "Carnitine palmitoyl transferase IA deficiency", "carnitine palmitoyl transferase IA deficiency", "Carnitine palmitoyltransferase deficiency type 1", "Carnitine palmitoyltransferase type I deficiency", "CPT1 - Carnitine palmitoyltransferase I deficiency", "Hepatic carnitine palmitoyltransferase 1 deficiency", "hepatic carnitine palmitoyltransferase 1 deficiency", "hepatic carnitine palmitoyl transferase 1 deficiency", "Hepatic carnitine palmitoyl transferase I deficiency", "Hepatic carnitine palmitoyl transferase 1 deficiency", "hepatic carnitine palmitoyl transferase I deficiency", "Carnitine palmitoyltransferase I deficiency (disorder)", "carnitine palmitoyltransferase deficiency 1 (diagnosis)", "Liver form of carnitine palmitoyltransferase deficiency", "CPTI - Carnitine palmitoyltransferase deficiency type I", "Liver Form of Carnitine Palmitoyltransferase Deficiency", "CPT1A disorder of carnitine cycle and carnitine transport", "disorder of carnitine cycle and carnitine transport caused by mutation in CPT1A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carnitine palmitoyl transferase 1A deficiency", "shortest_name_length": 12}
{"curie": "MONDO:0014405", "names": ["SAVI", "AUTOINFLAMMATORY-VASCULOPATHY SYNDROME", "STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET", "STING-Associated Vasculopathy, Infantile-Onset", "STING-associated vasculopathy, infantile-onset", "STING-associated vasculopathy with onset in infancy", "STING-associated vasculopathy with onset in infancy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "STING-associated vasculopathy with onset in infancy", "shortest_name_length": 4}
{"curie": "MONDO:0007961", "names": ["megalencephaly, autosomal dominant", "MEGALENCEPHALY, AUTOSOMAL DOMINANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "megalencephaly, autosomal dominant", "shortest_name_length": 34}
{"curie": "UMLS:C0856137", "names": ["Uterine fibroids aggravated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine fibroids aggravated", "shortest_name_length": 27}
{"curie": "MONDO:0015008", "names": ["AI1J", "amelogenesis imperfecta type 1J", "amelogenesis imperfecta, type 1J", "amelogenesis imperfecta, type ij", "amelogenesis imperfecta, type Ij", "AMELOGENESIS IMPERFECTA, TYPE IJ", "Amelogenesis imperfecta, type IJ"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amelogenesis imperfecta, type 1J", "shortest_name_length": 4}
{"curie": "UMLS:C0334296", "names": ["Solid carcinoma", "solid carcinoma", "Solid Carcinoma", "Solid carcinoma NOS", "Solid carcinoma, NOS", "solid carcinoma (diagnosis)", "Solid carcinoma with mucin formation", "Solid carcinoma (morphologic abnormality)", "Solid adenocarcinoma with mucin formation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Solid carcinoma", "shortest_name_length": 15}
{"curie": "MONDO:0032883", "names": ["IDDBCS", "intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH BEHAVIORAL ABNORMALITIES AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT SEIZURES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures", "shortest_name_length": 6}
{"curie": "MONDO:0007993", "names": ["MLRD", "microgastria limb reduction defect", "Microgastria limb reduction defect", "microgastria-limb reduction defect syndrome", "Microgastria-limb reduction defects association", "microgastria-limb reduction defects association", "MICROGASTRIA-LIMB REDUCTION DEFECTS ASSOCIATION", "Congenital microgastria and limb reduction defects", "congenital microgastria and limb reduction defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microgastria-limb reduction defect syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0011412", "names": ["FENIB", "ENCEPHALOPATHY, FAMILIAL, WITH COLLINS BODIES", "encephalopathy, familial, with Collins bodies", "Encephalopathy, familial, with Collins bodies", "Familial Dementia with Neuroserpin Inclusion Bodies", "Familial dementia with neuroserpin inclusion bodies", "Familial encephalopathy with neuroserpin inclusion bodies", "familial encephalopathy with neuroserpin inclusion bodies", "Encephalopathy, Familial, With Neuroserpin Inclusion Bodies", "encephalopathy, familial, with neuroserpin inclusion bodies", "ENCEPHALOPATHY, FAMILIAL, WITH NEUROSERPIN INCLUSION BODIES", "Familial encephalopathy with neuroserpin inclusion bodies (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial encephalopathy with neuroserpin inclusion bodies", "shortest_name_length": 5}
{"curie": "UMLS:C2062513", "names": ["Renal Hemangioma", "Renal hemangioma", "renal hemangioma", "Renal haemangioma", "Kidney Hemangioma", "benign hemangioma of kidney", "benign hemangioma of kidney (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal hemangioma", "shortest_name_length": 16}
{"curie": "UMLS:C4724873", "names": ["Refractory Thymic Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Thymic Carcinoma", "shortest_name_length": 27}
{"curie": "OMIM:615749", "names": ["ECULIZUMAB, POOR RESPONSE TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 28}
{"curie": "UMLS:C1336272", "names": ["Stage III Testicular Nonseminomatous Germ Cell Tumor", "Stage III Testicular Non-Seminomatous Germ Cell Tumor", "Stage III Testicular Non-Seminomatous Germ Cell Tumor AJCC v6", "Stage III Testicular Non-Seminomatous Germ Cell Tumor AJCC v7", "Stage III Testicular Non-Seminomatous Germ Cell Tumor AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Testicular Non-Seminomatous Germ Cell Tumor AJCC v6 and v7", "shortest_name_length": 52}
{"curie": "MONDO:0007675", "names": ["GLUTAMIC ACID DECARBOXYLASE, BRAIN, MEMBRANE FORM", "glutamic acid decarboxylase, brain, membrane form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glutamic acid decarboxylase, brain, membrane form", "shortest_name_length": 49}
{"curie": "MONDO:0000728", "names": ["PTOSIS", "ptosis", "Ptosis", "Prolapse", "PROLAPSE", "prolapse", "Eye drop", "Prolapses", "prolapses", "Procidentia", "procidentia", "eyelid droop", "procidentias", "Eyelid Ptoses", "Ptosis;eyelid", "Eyelid Ptosis", "Eyelid ptosis", "EYELID PTOSIS", "eyelid ptosis", "Ptosis eyelid", "Droopy eyelid", "droopy eyelid", "Droopy eyelids", "drooped eyelid", "Ptosis, Eyelid", "BLEPHAROPTOSIS", "droopy eyelids", "Ptoses, Eyelid", "ptosis; eyelid", "eyelids ptosis", "blepharoptosis", "eyelid; ptosis", "Blepharoptoses", "Blepharoptosis", "Drooping;eyelid", "Drooping eyelid", "eyelid drooping", "drooping eyelid", "ptosis (disease)", "ptosis of eyelid", "Ptosis of eyelid", "Caudal displacement", "caudal displacement", "Upper eyelid drooped", "Displacement, caudal", "Ptosis of eyelid, NOS", "Downward displacement", "Displacement downward", "Drooping upper eyelid", "Inferior displacement", "Displacement, inferior", "ptosis (physical finding)", "drooping eyelid (symptom)", "Ptosis of eyelid (disorder)", "ptosis of eyelid (diagnosis)", "Unspecified ptosis of eyelid", "Ptosis of eyelid, unspecified", "Prolapse (morphologic abnormality)", "Unspecified ptosis of unspecified eyelid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ptosis", "shortest_name_length": 6}
{"curie": "MONDO:0003519", "names": ["MAC", "Eccrine epithelioma", "malignant syringoma", "Eccrine Epithelioma", "Malignant syringoma", "syringoma, malignant", "Syringomatous carcinoma", "syringomatous carcinoma", "Syringomatous Carcinoma", "carcinomas syringomatous", "Eccrine epithelioma of skin", "Syringoid eccrine carcinoma", "microcystic adnexal carcinoma", "Microcystic adnexal carcinoma", "Microcystic Adnexal Carcinoma", "Microcystic Adnexal carcinoma", "sclerosing sweat duct carcinoma", "Sclerosing sweat duct carcinoma", "Syringomatous sweat duct carcinoma", "sclerosing carcinoma of sweat duct", "microcystic adnexal carcinoma of skin", "Microcystic adnexal carcinoma of skin", "Eccrine epithelioma of skin (disorder)", "Eccrine epithelioma (morphologic abnormality)", "sclerosing carcinoma of sweat duct (diagnosis)", "Microcystic adnexal carcinoma of skin (disorder)", "Sclerosing sweat duct carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant syringoma", "shortest_name_length": 3}
{"curie": "MONDO:0014528", "names": ["caid", "CAID", "CAID syndrome", "caid syndrome", "CHRONIC ATRIAL AND INTESTINAL DYSRHYTHMIA", "chronic atrial and intestinal dysrhythmia", "Chronic atrial and intestinal dysrhythmia", "Cohesinopathy affecting heart and gut rhythm", "chronic atrial intestinal dysrhythmia syndrome", "chronic atrial and intestinal dysrhythmia syndrome", "Chronic atrial and intestinal dysrhythmia syndrome", "Chronic atrial and intestinal dysrhythmia (disorder)", "chronic atrial dysrhythmia-intestinal motility disorder", "Chronic atrial dysrhythmia-intestinal motility disorder", "CAID (chronic atrial and intestinal dysrhythmia) syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic atrial and intestinal dysrhythmia", "shortest_name_length": 4}
{"curie": "UMLS:C2347747", "names": ["Classical Hodgkin Lymphoma", "Adult Classic Hodgkin Lymphoma", "Adult Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Classical Hodgkin Lymphoma", "shortest_name_length": 26}
{"curie": "MONDO:0030087", "names": ["PNDM2", "DEND1", "DIABETES MELLITUS, PERMANENT NEONATAL 2", "diabetes mellitus, permanent neonatal 2", "DIABETES MELLITUS, PERMANENT NEONATAL, 2", "DEVELOPMENTAL DELAY, EPILEPSY, AND NEONATAL DIABETES 1", "Developmental Delay, Epilepsy, and Neonatal Diabetes 1", "diabetes, permanent neonatal 2, with or without neurologic features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diabetes mellitus, permanent neonatal 2", "shortest_name_length": 5}
{"curie": "UMLS:C4053514", "names": ["NCMH", "Nasal Chondromesenchymal Hamartoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasal Chondromesenchymal Hamartoma", "shortest_name_length": 4}
{"curie": "UMLS:C2984533", "names": ["Stage II Gallbladder Cancer", "stage IIB gallbladder cancer", "stage IIA gallbladder cancer", "Gallbladder Cancer Stage II AJCC v6", "Stage II Gallbladder Cancer AJCC v6", "Stage II Gallbladder Carcinoma AJCC v6", "Gallbladder Carcinoma Stage II AJCC v6", "Stage II Carcinoma of Gallbladder AJCC v6", "Stage II Carcinoma of the Gallbladder AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Gallbladder Cancer AJCC v6", "shortest_name_length": 27}
{"curie": "MONDO:0015991", "names": ["CITRULLINURIA", "citrullinuria", "Citrullinemia", "CITRULLINEMIA", "citrullinemia", "Citrullinuria", "ASS deficiency", "citrullinaemia", "Citrullinurias", "ass deficiency", "Citrullinemias", "ASS DEFICIENCY", "Citrullinaemia", "ASS Deficiency", "ASAS deficiency", "Deficiency, ASS", "ASS Deficiencies", "classic citrullinemia", "Citrullinuria (finding)", "ASA synthase deficiency", "Citrulline high in urine", "Citrullinemia (disorder)", "citrullinemia (diagnosis)", "Argininosuccinase deficiency", "Argininosuccinate synthase deficiency", "Arginosuccinate synthetase deficiency", "arginosuccinate synthetase deficiency", "ARGININOSUCCINATE SYNTHETASE DEFICIENCY", "Argininosuccinate synthetase deficiency", "Argininosuccinate Synthetase Deficiency", "Deficiency of argininosuccinate synthase", "Deficiency, Argininosuccinate Synthetase", "deficiency of citrulline-aspartate ligase", "Deficiency of citrulline-aspartate ligase", "Argininosuccinate Synthetase Deficiencies", "Deficiencies, Argininosuccinate Synthetase", "Argininosuccinic Acid Synthetase Deficiency", "Argininosuccinate Synthase Deficiency Disease", "Deficiency Disease, Argininosuccinate Synthase", "Argininosuccinic Acid Synthase Deficiency Disease", "Deficiency Disease, Argininosuccinic Acid Synthase", "Argininosuccinic Acid Synthetase Deficiency Disease", "Deficiency of argininosuccinate synthase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "citrullinemia", "shortest_name_length": 13}
{"curie": "MONDO:0013607", "names": ["DCML", "IMD21", "MonoMAC", "MONOMAC", "GATA2 DEFICIENCY", "MonoMAC syndrome", "GATA2 deficiency", "MonoMac Syndrome", "MonoMAC Syndrome", "GATA2 Deficiency", "MonoMac Syndromes", "GATA2 Deficiencies", "IMMUNODEFICIENCY 21", "immunodeficiency 21", "Immunodeficiency 21", "GATA2 Haploinsufficiency", "immunodeficiency type 21", "Immunodeficiency type 21", "GATA2 Haploinsufficiencies", "Monocytopenia with susceptibility to infections", "monocytopenia with susceptibility to infections", "MONOCYTOPENIA AND MYCOBACTERIAL INFECTION SYNDROME", "monocytopenia and mycobacterial infection syndrome", "Monocytopenia and Mycobacterial Infection Syndrome", "Monocytopenia and mycobacterial infection syndrome", "dendritic cell, monocyte, B and NK lymphoid deficiency", "Dendritic cell, monocyte, B and NK lymphoid deficiency", "monocyte - B - natural killer - dendritic cell deficiency", "Monocytopenia with susceptibility to infections (disorder)", "monocyte-B-natural killer-dendritic cell deficiency syndrome", "Monocyte-B natural killer dendritic cell deficiency syndrome", "Monocyte-B-natural killer-dendritic cell deficiency syndrome", "Dendritic cell, monocyte, B lymphocyte, and natural Killer lymphocyte deficiency", "DENDRITIC CELL, MONOCYTE, B LYMPHOCYTE, AND NATURAL KILLER LYMPHOCYTE DEFICIENCY", "Combined immunodeficiency with susceptibility to mycobacterial, viral and fungal infection", "combined immunodeficiency with susceptibility to mycobacterial, viral and fungal infections", "Combined immunodeficiency with susceptibility to mycobacterial, viral and fungal infections", "COMBINED IMMUNODEFICIENCY WITH SUSCEPTIBILITY TO MYCOBACTERIAL, VIRAL, AND FUNGAL INFECTIONS", "combined immunodeficiency with susceptibility to mycobacterial, viral, and fungal infections", "monocytopenia with susceptibility to mycobacterial, fungal, and Papillomavirus infections and myelodysplasia", "MONOCYTOPENIA WITH SUSCEPTIBILITY TO MYCOBACTERIAL, FUNGAL, AND PAPILLOMAVIRUS INFECTIONS AND MYELODYSPLASIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "monocytopenia with susceptibility to infections", "shortest_name_length": 4}
{"curie": "UMLS:C0276228", "names": ["HSV keratoconjunctivitis", "herpetic keratoconjunctivitis", "Herpetic keratoconjunctivitis", "Herpes simplex keratoconjunctivitis", "keratoconjunctivitis herpes simplex", "Herpes simplex keratoconjunctivitis (disorder)", "Herpes simplex keratoconjunctivitis (diagnosis)", "herpes; keratoconjunctivitis (h.simplex) (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Herpes simplex keratoconjunctivitis", "shortest_name_length": 24}
{"curie": "MONDO:0016467", "names": ["Acutane embryopathy", "accutane embryopathy", "Accutane embryopathy", "isotretinoin syndrome", "Retinoids embryopathy", "Isotretinoin syndrome", "Fetal Retinoid Syndrome", "fetal retinoid syndrome", "fetal Accutane syndrome", "fetal accutane syndrome", "Fetal retinoid syndrome", "Isotretinoin embryopathy", "isotretinoin embryopathy", "Fetal vitamin A syndrome", "Foetal retinoid syndrome", "Retinoic Acid Embryopathy", "Accutane fetal effects of", "Retinoic acid embryopathy", "retinoic acid embryopathy", "Fetal isoretinoin syndrome", "Fetal Isotretinoin Syndrome", "fetal isotretinoin syndrome", "Accutane dysmorphic syndrome", "Accutane-exposed pregnancies", "accutane dysmorphic syndrome", "Isotretinoin fetal effects of", "isotretinoin (ITR) embryopathy", "isotretinoin teratogen syndrome", "Isotretinoin teratogen syndrome", "isotretinoin dysmorphic syndrome", "Embryopathy caused by isotretinoin", "isotretinoin (ITR) teratogen syndrome", "Isotretinoin (RoAccutane) embryopathy", "isotretinoin (ITR) dysmorphic syndrome", "Congenital malformation due to vitamin A", "Embryopathy caused by isotretinoin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isotretinoin syndrome", "shortest_name_length": 19}
{"curie": "MONDO:0015001", "names": ["ATFB18", "MYL4 familial atrial fibrillation", "ATRIAL FIBRILLATION, FAMILIAL, 18", "atrial fibrillation, familial, 18", "atrial fibrillation, familial, type 18", "atrial fibrillation, familial, 18; ATFB18", "familial atrial fibrillation caused by mutation in MYL4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial fibrillation, familial, 18", "shortest_name_length": 6}
{"curie": "UMLS:C4521624", "names": ["Stage II Sinonasal Cancer AJCC v8", "Stage II Sinonasal Cancer AJCC  v8", "Stage II Sinonasal Carcinoma AJCC v8", "Stage II Nasal Cavity and Paranasal Sinus Cancer", "Stage II Nasal Cavity and Paranasal Sinus Cancer AJCC v8", "Stage II Nasal Cavity and Paranasal Sinus Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Nasal Cavity and Paranasal Sinus Cancer AJCC v8", "shortest_name_length": 33}
{"curie": "UMLS:C0079173", "names": ["Craniomandibular Disease", "Craniomandibular Diseases", "Craniomandibular Disorder", "Disease, Craniomandibular", "Diseases, Craniomandibular", "Disorder, Craniomandibular", "Craniomandibular Disorders", "Disorders, Craniomandibular"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Craniomandibular Disorders", "shortest_name_length": 24}
{"curie": "MONDO:0001075", "names": ["oily stools", "FATTY STOOL", "fatty stool", "Steatorrhea", "steatorrhea", "STEATORRHEA", "stool fatty", "Fatty stool", "Greasy stool", "FATTY STOOLS", "steatorrhoea", "Fat in feces", "STEATORRHOEA", "Steatorrhoea", "fatty stools", "Fatty stools", "Fat in faeces", "greasy stools", "Greasy stools", "Steatorrhea, NOS", "Steatorrhoea, NOS", "Fecal fat increased", "FECAL FAT INCREASED", "Chronic steatorrhea", "STOOL FAT INCREASED", "Faecal fat increased", "Chronic steatorrhoea", "FAECAL FAT INCREASED", "Fatty stool (finding)", "fatty stool (finding)", "steatorrhea (disease)", "fatty stools (symptom)", "Chronic steatorrhea (disorder)", "Chronic steatorrhea (diagnosis)", "Greasy/oily stools (steatorrhea)", "malabsorption syndrome chronic steatorrhea"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "steatorrhea", "shortest_name_length": 11}
{"curie": "MONDO:0011716", "names": ["AHL", "Ahl", "AHLE", "hurst disease", "Hurst Disease", "Hurst Syndrome", "Disease, Hurst", "Hursts Disease", "Hurst syndrome", "Syndrome, Hurst", "Hurst's disease", "hurst's disease", "Hurst's Disease", "Disease, Hurst's", "Weston-Hurst syndrome", "Acute hemorrhagic leukencephalitis", "ear-patella-short stature syndrome", "acute hemorrhagic encephalomyelitis", "ACUTE HEMORRHAGIC LEUKOENCEPHALITIS", "Acute Hemorrhagic Leukoencephalitis", "acute hemorrhagic leukoencephalitis", "Acute Hemorrhagic Encephalomyelitis", "Acute hemorrhagic leukoencephalitis", "Acute hemorrhagic leucoencephalitis", "Leukoencephalitis Acuta Hemorrhagica", "Hemorrhagic Leukoencephalitis, Acute", "Hemorrhagic Encephalomyelitis, Acute", "Leukoencephalitis, Acute Hemorrhagic", "Acute haemorrhagic leucoencephalitis", "Encephalomyelitis, Acute Hemorrhagic", "Acute haemorrhagic leukoencephalitis", "LEUKOENCEPHALITIS, HEMORRHAGIC, ACUTE", "Acute Hemorrhagic Leukoencephalitides", "Acute Hemorrhagic Encephalomyelitides", "Hemorrhagic Leukoencephalitides, Acute", "Encephalomyelitides, Acute Hemorrhagic", "Hemorrhagic Encephalomyelitides, Acute", "Leukoencephalitides, Acute Hemorrhagic", "ear-patella-short stature (EPS) syndrome", "microtia-absent patellae-micrognathia syndrome", "Acute hemorrhagic leukoencephalitis (disorder)", "acute necrotizing hemorrhagic leukoencephalitis", "Encephalomyelitis, Acute Necrotizing Hemorrhagic", "ENCEPHALOMYELITIS, NECROTIZING HEMORRHAGIC, ACUTE", "Acute hemorrhagic leukoencephalitis of Weston Hurst", "acute haemorrhagic leucoencephalitis of Weston Hurst", "Acute haemorrhagic leucoencephalitis of Weston Hurst"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute hemorrhagic leukoencephalitis", "shortest_name_length": 3}
{"curie": "UMLS:C4521721", "names": ["Stage IVA Esophageal Adenocarcinoma", "Postneoadjuvant Therapy Stage IVA Esophageal Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postneoadjuvant Therapy Stage IVA Esophageal Adenocarcinoma AJCC v8", "shortest_name_length": 35}
{"curie": "UMLS:C0267406", "names": ["mesenteric infarction", "Mesenteric infarction", "Infarction mesenteric", "Mesenteric Infarction", "INFARCTION MESENTERIC", "infarction; mesenteric", "mesenteric; infarction", "Mesenteric infarction, NOS", "Mesenteric infarction (disorder)", "mesenteric infarction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mesenteric infarction", "shortest_name_length": 21}
{"curie": "MONDO:0017806", "names": ["15q overgrowth syndrome", "15q26 overgrowth syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "15q overgrowth syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0014146", "names": ["HYPOC2", "autosomal dominant hypocalcemia 2", "hypocalcemia, autosomal dominant 2", "HYPOCALCEMIA, AUTOSOMAL DOMINANT 2", "autosomal dominant hypocalcemia type 2", "hypocalcemia, autosomal dominant type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant hypocalcemia 2", "shortest_name_length": 6}
{"curie": "UMLS:C0854238", "names": ["Diverticulum intestinal hemorrhagic", "Diverticulum intestinal haemorrhagic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diverticulum intestinal hemorrhagic", "shortest_name_length": 35}
{"curie": "UMLS:C1443892", "names": ["Chronic Q Fever", "Chronic Q fever", "Fever, Chronic Q", "Q Fever, Chronic", "Chronic Q Fevers", "Q Fevers, Chronic", "Fevers, Chronic Q", "Chronic Q fever (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic Q Fever", "shortest_name_length": 15}
{"curie": "UMLS:C1520074", "names": ["Vulvar Blue Nevus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Blue Nevus", "shortest_name_length": 17}
{"curie": "UMLS:C5420032", "names": ["Sinonasal NUT Carcinoma", "Nasal Cavity and Paranasal Sinus NUT Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal NUT Carcinoma", "shortest_name_length": 23}
{"curie": "MONDO:0004343", "names": ["Acinar Cell Cystadenocarcinoma", "Acinar cell cystadenocarcinoma", "acinar cell cystadenocarcinoma", "pancreatic acinar cell cystadenocarcinoma", "Pancreatic Acinar Cell Cystadenocarcinoma", "acinar cell cystadenocarcinoma (diagnosis)", "Acinar Cell Cystadenocarcinoma of Pancreas", "acinar cell cystadenocarcinoma of pancreas", "acinar cell cystadenocarcinoma of the pancreas", "Acinar Cell Cystadenocarcinoma of the Pancreas", "acinar cell cystadenocarcinoma of pancreas (diagnosis)", "acinar cell cystadenocarcinoma (morphologic abnormality)", "Acinar cell cystadenocarcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic acinar cell cystadenocarcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0009808", "names": ["osteoid osteoma", "OSTEOID OSTEOMA", "Osteoid Osteoma", "Osteoid osteoma", "osteoma osteoid", "osteoid osteomas", "Osteoid Osteomas", "Osteoma, Osteoid", "Osteomas, Osteoid", "Osteoid osteoma NOS", "Osteoid osteoma, NOS", "osteoid osteoma (disease)", "benign osteoid osteoma of bone", "Osteoid osteoma (morphologic abnormality)", "benign osteoid osteoma of bone (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteoid osteoma", "shortest_name_length": 15}
{"curie": "UMLS:C5206781", "names": ["Refractory Malignant Myoepithelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Malignant Myoepithelioma", "shortest_name_length": 35}
{"curie": "UMLS:C2698997", "names": ["Craniopharyngioma malignant", "CRANIOPHARYNGIOMA, MALIGNANT", "Carcinoma Arising from Craniopharyngioma", "Carcinoma Arising From Craniopharyngioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Craniopharyngioma malignant", "shortest_name_length": 27}
{"curie": "MONDO:0029144", "names": ["EHMTO", "MTO DEFICIENCY", "MTO Deficiency", "MTO-deficiency", "Methanethiol oxidase deficiency", "METHANETHIOL OXIDASE DEFICIENCY", "METHANETHIOL Oxidase Deficiency", "Autosomal recessive extra-oral halitosis", "extraoral halitosis due to MTO deficiency", "EXTRAORAL HALITOSIS WITH DIMETHYLSULFOXIDURIA", "extraoral halitosis with dimethylsulfoxiduria", "extraoral halitosis due to methanethiol oxidase deficiency", "EXTRAORAL HALITOSIS DUE TO METHANETHIOL OXIDASE DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extraoral halitosis due to methanethiol oxidase deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0014687", "names": ["RP73", "retinitis pigmentosa 73", "RETINITIS PIGMENTOSA 73", "HGSNAT retinitis pigmentosa", "retinitis pigmentosa type 73", "retinitis pigmentosa caused by mutation in HGSNAT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 73", "shortest_name_length": 4}
{"curie": "UMLS:C0279648", "names": ["Acute Eosinophilic Leukemia", "Childhood Acute Eosinophilic Leukemia", "Pediatric Acute Eosinophilic Leukemia", "pediatric acute eosinophilic leukemia", "childhood acute eosinophilic leukemia", "leukemia, childhood acute eosinophilic", "eosinophilic leukemia, childhood acute", "acute eosinophilic leukemia, childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Acute Eosinophilic Leukemia", "shortest_name_length": 27}
{"curie": "UMLS:C5420395", "names": ["Lung Alveolar Soft Part Sarcoma", "Primary Lung Alveolar Soft Part Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Alveolar Soft Part Sarcoma", "shortest_name_length": 31}
{"curie": "UMLS:C0235984", "names": ["blocked salivary duct", "Blocked;salivary duct", "blocked ducts salivary", "Salivary duct obstruction", "SALIVARY DUCT OBSTRUCTION", "salivary duct obstruction", "salivary duct; obstruction", "obstruction; salivary duct", "obstruction of salivary duct", "Obstruction of salivary duct", "Salivary gland duct obstruction", "Obstruction of salivary duct, NOS", "Obstruction of salivary duct (disorder)", "obstruction of salivary duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Obstruction of salivary duct", "shortest_name_length": 21}
{"curie": "MONDO:0030465", "names": ["CTRCT49", "cataract 49", "CATARACT 49", "CARARACT 49, POSTERIOR"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 49", "shortest_name_length": 7}
{"curie": "UMLS:C0854729", "names": ["Spinal Vascular Disorder", "Spinal vascular disorder", "Spinal vascular disorder NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spinal vascular disorder", "shortest_name_length": 24}
{"curie": "UMLS:C5420643", "names": ["Non-Inflammatory Female Reproductive System Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Inflammatory Female Reproductive System Disorder", "shortest_name_length": 52}
{"curie": "OMIM:191540", "names": ["UOX", "URICASE", "URATE OXIDASE, PSEUDOGENE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 3}
{"curie": "UMLS:C1334384", "names": ["Leiomyosarcoma NCI Grade 3", "Leiomyosarcoma NCI Grade III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leiomyosarcoma NCI Grade 3", "shortest_name_length": 26}
{"curie": "MONDO:0014872", "names": ["CSNB1H", "congenital stationary night blindness 1H", "GNB3 congenital stationary night blindness", "congenital stationary night blindness type 1H", "night blindness, congenital stationary, type 1H", "NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1H", "congenital stationary night blindness caused by mutation in GNB3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital stationary night blindness 1H", "shortest_name_length": 6}
{"curie": "UMLS:C3897232", "names": ["Untreated Giant Cell Glioblastoma", "Untreated Childhood Giant Cell Glioblastoma", "untreated childhood giant cell glioblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Untreated Childhood Giant Cell Glioblastoma", "shortest_name_length": 33}
{"curie": "UMLS:C0271000", "names": ["Metallosis", "Metallosis, NOS", "Metallosis (disorder)", "Metal Related Pathology"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metallosis", "shortest_name_length": 10}
{"curie": "UMLS:C1336312", "names": ["Stage II Mesothelioma", "Stage II Mesothelioma of Pleura", "stage II mesothelioma of pleura", "stage II malignant mesothelioma", "Stage II Mesothelioma of the Pleura", "stage II mesothelioma of the pleura", "stage II pleural mesothelioma AJCC v7", "Stage II Pleural Malignant Mesothelioma", "Stage II Pleural Malignant Mesothelioma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Pleural Malignant Mesothelioma AJCC v7", "shortest_name_length": 21}
{"curie": "MONDO:0020453", "names": ["partial anomalous pulmonary venous return", "Partial anomalous pulmonary venous return", "Partial anomalous pulmonary Venous return", "v.pulmonalis; anomaly connection, partial", "Partial Anomalous Pulmonary Venous Return", "Partial Anomalous Pulmonary Venous Connection", "Partial anomalous pulmonary venous connection", "anomaly; connection, pulmonary veins, partial", "Partial anomalous pulmonary Venous connection", "connection; pulmonary veins, anomaly, partial", "anomaly; pulmonary, venous connection, partial", "PAPVR - Partial anomalous pulmonary venous return", "Congenital partial pulmonary venous return anomaly", "congenital partial pulmonary venous return anomaly", "PAPVD - Partial anomalous pulmonary venous drainage", "partial anomalous pulmonary venous return (diagnosis)", "PAPVC - Partial anomalous pulmonary venous connection", "Partial anomalous pulmonary venous connection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital partial pulmonary venous return anomaly", "shortest_name_length": 41}
{"curie": "UMLS:C0729772", "names": ["Infective laryngitis", "Infective laryngitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infective laryngitis", "shortest_name_length": 20}
{"curie": "UMLS:C0334324", "names": ["mixed cell adenocarcinoma", "Mixed cell adenocarcinoma", "Mixed Cell Adenocarcinoma", "mixed cell adenocarcinoma (diagnosis)", "Mixed cell adenocarcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mixed cell adenocarcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0013784", "names": ["RMFSL", "lethal neonatal rigidity-multifocal seizure syndrome", "Lethal neonatal rigidity-multifocal seizure syndrome", "Lethal neonatal rigidity, multifocal seizure syndrome", "neonatal-onset encephalopathy with rigidity and seizures", "Lethal Neonatal Rigidity and Multifocal Seizure Syndrome", "RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL", "rigidity and multifocal seizure syndrome, lethal neonatal", "Lethal neonatal spasticity-epileptic encephalopathy syndrome", "lethal neonatal spasticity-epileptic encephalopathy syndrome", "Lethal neonatal spasticity, epileptic encephalopathy syndrome", "Lethal neonatal spasticity, epileptic encephalopathy syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal-onset encephalopathy with rigidity and seizures", "shortest_name_length": 5}
{"curie": "MONDO:0021461", "names": ["hypopharynx benign neoplasm", "Benign Tumor of Hypopharynx", "Benign Hypopharyngeal Tumor", "Benign tumor of hypopharynx", "benign hypopharyngeal tumor", "benign tumor of hypopharynx", "Benign tumour of hypopharynx", "Benign Hypopharyngeal Neoplasm", "Benign neoplasm of hypopharynx", "benign hypopharyngeal neoplasm", "Hypopharyngeal neoplasm benign", "benign neoplasm of hypopharynx", "Benign Neoplasm of Hypopharynx", "Benign hypopharyngeal neoplasm", "Benign tumor of laryngopharynx", "Benign Tumor of the Hypopharynx", "Benign tumour of laryngopharynx", "hypopharyngeal neoplasm, benign", "benign tumor of the hypopharynx", "Hypopharyngeal Neoplasm, Benign", "Benign Neoplasm of the Hypopharynx", "benign neoplasm of the hypopharynx", "Benign neoplasm of hypopharynx, NOS", "Benign neoplasm of the laryngopharynx", "Benign neoplasm of hypopharynx (disorder)", "benign neoplasm of hypopharynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of hypopharynx", "shortest_name_length": 27}
{"curie": "UMLS:C1709575", "names": ["Pleural Lymphoma", "Primary Pleural Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pleural Lymphoma", "shortest_name_length": 16}
{"curie": "UMLS:C0596402", "names": ["cytotoxicity", "Lytotoxicity", "Cytotoxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cytotoxicity", "shortest_name_length": 12}
{"curie": "UMLS:C4721922", "names": ["Stage 0 Penile Cancer", "Stage 0 Penile Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Penile Cancer AJCC v7", "shortest_name_length": 21}
{"curie": "MONDO:0008217", "names": ["KOSENOW SYNDROME", "Kosenow syndrome", "Kosenow Syndrome", "Scapuloiliac Dysostosis", "Scapuloiliac dysostosis", "SCAPULOILIAC DYSOSTOSIS", "Pelvis shoulder dysplasia", "Pelvis-Shoulder Dysplasia", "Pelvis-shoulder dysplasia", "PELVIS-SHOULDER DYSPLASIA", "pelvis-shoulder dysplasia", "Pelvis shoulder dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pelvis-shoulder dysplasia", "shortest_name_length": 16}
{"curie": "UMLS:C4316810", "names": ["graphospasm", "Writer Cramp", "cramps writer", "Writers Cramp", "writers cramp", "writers' cramp", "writer's cramp", "cramps writers", "Writer's cramp", "Writer's Cramp", "cramp writer's", "cramps writer's", "palsy scriveners", "organic writers' cramp"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Writer's Cramp", "shortest_name_length": 11}
{"curie": "MONDO:0004596", "names": ["cor pulmonale", "Cor pulmonale", "COR PULMONALE", "Cor Pulmonale", "pulmonale; cor", "cor; pulmonale", "Cor pulmonale NOS", "pulmonary heart disease", "PULMONARY HEART DISEASE", "Pulmonary Heart Disease", "CARDIOPULMONARY DISEASE", "disease heart pulmonary", "heart pulmonary disease", "Heart disease pulmonary", "Pulmonary heart disease", "DISEASE HEART PULMONARY", "cardiopulmonary disease", "Disease heart pulmonary", "Disease;heart;pulmonary", "HEART DISEASE PULMONARY", "Disease, Pulmonary Heart", "cardiopulmonary diseases", "Cor pulmonale (disorder)", "heart disease, pulmonary", "Pulmonary Heart Diseases", "disease, pulmonary heart", "pulmonary heart diseases", "Heart Disease, Pulmonary", "Diseases, Pulmonary Heart", "heart diseases, pulmonary", "diseases, pulmonary heart", "cor pulmonale (diagnosis)", "Heart Diseases, Pulmonary", "Cardiopulmonary disease or syndrome", "pulmonary heart diseases (diagnosis)", "Pulmonary heart disease, unspecified", "disease (or disorder); cardiopulmonary", "Cardiopulmonary Diseases and Syndromes", "disease (or disorder); heart, pulmonary", "disease (or disorder); pulmonary, heart disease", "Right heart failure due to pulmonary hypertension", "cardiac failure right heart due to pulmonary hypertension", "Right heart failure due to pulmonary hypertension (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cor pulmonale", "shortest_name_length": 13}
{"curie": "UMLS:C0860649", "names": ["Insomnia due to Organic Factor", "Insomnia due to organic factors"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Insomnia due to organic factors", "shortest_name_length": 30}
{"curie": "UMLS:C1442826", "names": ["newborn necrotizing enterocolitis", "Neonatal necrotising enterocolitis", "NEONATAL NECROTIZING ENTEROCOLITIS", "Necrotizing enterocolitis neonatal", "Neonatal necrotizing enterocolitis", "Necrotising enterocolitis neonatal", "Enterocolitis, Neonatal necrotizing", "Necrotizing enterocolitis in newborn", "Necrotizing enterocolitis of newborn", "NNE - Neonatal necrotising enterocolitis", "NNE - Neonatal necrotizing enterocolitis", "NNEC - Neonatal necrotising enterocolitis", "Necrotizing enterocolitis in newborn, NOS", "NNEC - Neonatal necrotizing enterocolitis", "newborn necrotizing enterocolitis (diagnosis)", "Neonatal necrotizing enterocolitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neonatal necrotizing enterocolitis", "shortest_name_length": 33}
{"curie": "UMLS:C5420454", "names": ["Recurrent Metastatic Malignant Neoplasm in the Leptomeninges"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Metastatic Malignant Neoplasm in the Leptomeninges", "shortest_name_length": 60}
{"curie": "UMLS:C5400424", "names": ["Labeled drug-drug interaction issue", "Labelled drug-drug interaction issue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Labeled drug-drug interaction issue", "shortest_name_length": 35}
{"curie": "UMLS:C3642330", "names": ["Vaginal Endometrioid Stromal Sarcoma", "Endometrioid Stromal Sarcoma of the Vagina", "Vaginal Low Grade Endometrioid Stromal Sarcoma", "Low Grade Endometrioid Stromal Sarcoma of the Vagina"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Low Grade Endometrioid Stromal Sarcoma", "shortest_name_length": 36}
{"curie": "UMLS:C5420398", "names": ["Locally Advanced Intrahepatic Cholangiocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Intrahepatic Cholangiocarcinoma", "shortest_name_length": 48}
{"curie": "MONDO:0041093", "names": ["central retinal vein occlusion with macular edema", "Central retinal vein occlusion with macular edema", "retinal vein occlusion, central with macular edema", "Central retinal vein occlusion with macular oedema", "Central retinal vein occlusion with macular edema (disorder)", "Central retinal vein occlusion with macular edema (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central retinal vein occlusion with macular edema", "shortest_name_length": 49}
{"curie": "UMLS:C4727947", "names": ["Hypophosphatemic osteomalacia", "Hypophosphataemic osteomalacia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypophosphatemic osteomalacia", "shortest_name_length": 29}
{"curie": "UMLS:C1393815", "names": ["Contraceptive device complication", "contraceptive device; complications"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Contraceptive device complication", "shortest_name_length": 33}
{"curie": "MONDO:0006067", "names": ["prostate colloid adenocarcinoma", "colloidal prostate adenocarcinoma", "Colloidal Prostate Adenocarcinoma", "colloid adenocarcinoma of prostate", "Colloid Adenocarcinoma of Prostate", "mucinous adenocarcinoma of prostate", "Mucinous Adenocarcinoma of Prostate", "colloidal adenocarcinoma of prostate", "Colloidal Adenocarcinoma of Prostate", "colloid adenocarcinoma of the prostate", "acinar colloid prostate adenocarcinoma", "acinar Colloid prostate adenocarcinoma", "Colloid Adenocarcinoma of the Prostate", "Acinar Colloid Prostate Adenocarcinoma", "Prostate Acinar Mucinous Adenocarcinoma", "acinar prostate mucinous adenocarcinoma", "Mucinous Adenocarcinoma of the Prostate", "mucinous adenocarcinoma of the prostate", "Acinar Prostate Mucinous Adenocarcinoma", "colloidal adenocarcinoma of the prostate", "Colloidal Adenocarcinoma of the Prostate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acinar prostate mucinous adenocarcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0009068", "names": ["MC4DN1", "COX DEFICIENCY", "COX deficiency", "Cox deficiency", "Cox Deficiency", "Deficiency, Cox", "Cox Deficiencies", "Deficiencies, Cox", "Complex IV deficiency", "complex iv deficiency", "Complex IV Deficiency", "Deficiency, Complex IV", "isolated COX deficiency", "Isolated COX deficiency", "Complex IV Deficiencies", "Deficiencies, Complex IV", "cytochrome oxidase deficiency", "Cytochrome Oxidase Deficiency", "Deficiency, Cytochrome Oxidase", "Oxidase Deficiency, Cytochrome", "CYTOCHROME c OXIDASE DEFICIENCY", "Cytochrome-c oxidase deficiency", "Cytochrome Oxidase Deficiencies", "Cytochrome C oxidase deficiency", "Cytochrome c oxidase deficiency", "cytochrome-c oxidase deficiency", "cytochrome c oxidase deficiency", "Cytochrome-C Oxidase Deficiency", "Cytochrome C Oxidase Deficiency", "c cytochrome deficiency oxidase", "cytochrome C oxidase deficiency", "Cytochrome-c Oxidase Deficiency", "cytochrome-C oxidase deficiency", "Oxidase Deficiency, Cytochrome-c", "Oxidase Deficiencies, Cytochrome", "Deficiency, Cytochrome c Oxidase", "Deficiency, Cytochrome-c Oxidase", "Deficiencies, Cytochrome Oxidase", "Cytochrome-c Oxidase Deficiencies", "Oxidase Deficiencies, Cytochrome-c", "Deficiencies, Cytochrome-c Oxidase", "mitochondrial Complex 4 deficiency", "MITOCHONDRIAL COMPLEX IV DEFICIENCY", "mitochondrial complex IV deficiency", "Mitochondrial Complex IV Deficiency", "Mitochondrial complex IV deficiency", "COX - Cytochrome C oxidase deficiency", "cytochrome-c oxidase deficiency disease", "isolated cytochrome C oxidase deficiency", "Isolated cytochrome C oxidase deficiency", "Cytochrome-c oxidase deficiency (disorder)", "Mitochondrial Complex IV Deficiency, Nuclear Type 1", "MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 1", "mitochondrial complex IV deficiency, nuclear type 1", "Complex 4 mitochondrial respiratory chain deficiency", "deficiency of mitochondrial respiratory chain complex4", "Isolated mitochondrial respiratory chain complex IV deficiency", "isolated mitochondrial respiratory chain complex IV deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cytochrome-c oxidase deficiency disease", "shortest_name_length": 6}
{"curie": "UMLS:C1883029", "names": ["Signet Ring Cell Lobular Breast Carcinoma", "Invasive Breast Lobular Carcinoma, Signet Ring Variant", "Invasive Lobular Breast Carcinoma, Signet Ring Variant", "Invasive Breast Lobular Carcinoma, Signet-Ring Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Invasive Breast Lobular Carcinoma, Signet Ring Variant", "shortest_name_length": 41}
{"curie": "MONDO:0008031", "names": ["FSHD2", "FSHD1B", "FSHMD1B", "Fshd2, digenic", "FSHD2, DIGENIC", "Facioscapulohumeral Muscular Dystrophy 2", "facioscapulohumeral muscular dystrophy 2", "facioscapulohumeral muscular dystrophy 1B", "FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1B", "Facioscapulohumeral Muscular Dystrophy 1B", "facioscapulohumeral muscular dystrophy type 2", "SMCHD1 facioscapulohumeral muscular dystrophy", "muscular dystrophy, facioscapulohumeral, type 2", "MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 2", "MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1B", "muscular dystrophy, facioscapulohumeral, type 1B", "Muscular Dystrophy, Facioscapulohumeral, Type 1B", "facioscapulohumeral muscular dystrophy 2, digenic", "FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 2, DIGENIC", "facioscapulohumeral muscular dystrophy type 2 (diagnosis)", "facioscapulohumeral muscular dystrophy caused by mutation in SMCHD1", "fascioscapulohumeral muscular dystrophy 2, digenic, digenic dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "facioscapulohumeral muscular dystrophy 2", "shortest_name_length": 5}
{"curie": "UMLS:C1709650", "names": ["Presymptomatic Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Presymptomatic Cancer", "shortest_name_length": 21}
{"curie": "EFO:0010698", "names": ["retinal break\"@e"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal break\"@e", "shortest_name_length": 16}
{"curie": "UMLS:C1336519", "names": ["Sublingual Gland Adenocarcinoma", "adenocarcinoma of sublingual gland", "Adenocarcinoma of Sublingual Gland", "Adenocarcinoma of the Sublingual Gland", "adenocarcinoma of sublingual gland (diagnosis)", "malignant salivary gland neoplasm sublingual adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenocarcinoma of sublingual gland", "shortest_name_length": 31}
{"curie": "MONDO:0001128", "names": ["nasal cavity cancer", "cancer cavity nasal", "cancer of nasal cavity", "Cancer of the nasal cavity", "malignant nasal cavity tumor", "Malignant Nasal Cavity Tumor", "nasal cavity cancer (diagnosis)", "malignant nasal cavity neoplasm", "malignant tumor of nasal cavity", "Malignant tumor of nasal cavity", "Malignant Tumor of Nasal Cavity", "Malignant Nasal Cavity Neoplasm", "Malignant tumour of nasal cavity", "malignant neoplasm of nasal cavity", "Malignant Neoplasm of Nasal Cavity", "Malignant neoplasm of nasal cavity", "Malignant Tumor of the Nasal Cavity", "malignant tumor of the nasal cavity", "malignant neoplasm of nasal cavities", "Malignant neoplasm of nasal cavities", "malignant neoplasm of the nasal cavity", "Malignant Neoplasm of the Nasal Cavity", "Malignant neoplasm of nasal cavity, NOS", "Malignant tumor of nasal cavity (disorder)", "malignant neoplasm of nasal cavity (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasal cavity cancer", "shortest_name_length": 19}
{"curie": "MONDO:0012063", "names": ["Morava Mehes syndrome", "Morava-Mehes syndrome", "ULNAR/FIBULAR RAY DEFECT AND BRACHYDACTYLY", "ulnar/fibular RAY defect and brachydactyly", "Ulnar-Fibular Ray Defect and Brachydactyly", "Ulnar/fibula ray defect-brachydactyly syndrome", "ulnar/fibula ray defect-brachydactyly syndrome", "Ulna fibula ray defect and brachydactyly syndrome", "Ulna fibula ray defect and brachydactyly syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ulnar/fibula ray defect-brachydactyly syndrome", "shortest_name_length": 21}
{"curie": "UMLS:C2981718", "names": ["stage IIIA mycosis fungoides/Sezary syndrome", "Stage IIIA Mycosis Fungoides and Sezary Syndrome", "Stage IIIA Mycosis Fungoides and Sézary Syndrome", "stage IIIA mycosis fungoides and Sezary syndrome AJCC v7", "Stage IIIA Mycosis Fungoides and Sezary Syndrome AJCC v7", "Stage IIIA Mycosis Fungoides and Sézary Syndrome AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Mycosis Fungoides and Sezary Syndrome AJCC v7", "shortest_name_length": 44}
{"curie": "UMLS:C0271674", "names": ["Asymmetric diabetic proximal motor neuropathy", "Asymmetric Diabetic Proximal Motor Neuropathy", "Asymmetric proximal motor neuropathy with diabetes mellitus", "Asymmetric proximal motor neuropathy due to diabetes mellitus", "Asymmetric proximal motor neuropathy due to diabetes mellitus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Asymmetric Diabetic Proximal Motor Neuropathy", "shortest_name_length": 45}
{"curie": "MONDO:0013188", "names": ["CAMRQ3", "CA8 dysequilibrium syndrome", "dysequilibrium syndrome caused by mutation in CA8", "cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3", "CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 3", "Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3", "cerebellar ataxia, mental retardation, and dysequilibrium syndrome type 3", "cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 3", "cerebellar ataxia, intellectual disability, and dysequilibrium syndrome type 3", "CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDAL LOCOMOTION 3", "cerebellar ataxia and mental retardation with or without quadrupedal locomotion 3", "Cerebellar Ataxia And Mental Retardation With Or Without Quadrupedal Locomotion 3", "CEREBELLAR ATAXIA, IMPAIRED INTELLECTUAL DEVELOPMENT, AND DYSEQUILIBRIUM SYNDROME 3", "cerebellar ataxia and intellectual disability with or without quadrupedal locomotion 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 3", "shortest_name_length": 6}
{"curie": "MONDO:0007627", "names": ["FFDD1", "Type 1 FFDD", "FFDD type I", "FFDD, Type 1", "FFDD, type 1", "BRAUER SYNDROME", "Brauer Syndrome", "Brauer syndrome", "Syndrome, Brauer", "Focal Facial Dermal Dysplasia 1", "bitemporal aplasia cutis congenita", "Bitemporal aplasia cutis congenita", "Bitemporal Aplasia Cutis Congenita", "BITEMPORAL APLASIA CUTIS CONGENITA", "Focal facial dermal dysplasia type 1", "Focal facial dermal dysplasia type I", "focal facial dermal dysplasia type I", "Focal Facial Dermal Dysplasia Type 1", "focal facial dermal dysplasia type 1", "Focal facial dermal dysplasia 1 Brauer type", "Focal facial dermal dysplasia 1, Brauer type", "focal facial dermal dysplasia 1, Brauer type", "FOCAL FACIAL DERMAL DYSPLASIA 1, BRAUER TYPE", "Focal facial dermal dysplasia type I (disorder)", "hereditary symmetrical aplastic nevi of temples", "HEREDITARY SYMMETRICAL APLASTIC NEVI OF TEMPLES", "Hereditary Symmetrical Aplastic Nevi of Temples", "FFDD type 1 - focal facial dermal dysplasia type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal facial dermal dysplasia type I", "shortest_name_length": 5}
{"curie": "UMLS:C4524895", "names": ["Anal Cancer by AJCC v8 Stage", "Anal Carcinoma by AJCC v8 Stage", "Anal Canal and Perianal (Anal Margin) Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anal Cancer by AJCC v8 Stage", "shortest_name_length": 28}
{"curie": "MONDO:0008524", "names": ["syringomas, multiple", "Syringomas, Multiple", "SYRINGOMAS, MULTIPLE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syringomas, multiple", "shortest_name_length": 20}
{"curie": "UMLS:C0030790", "names": ["pelvis infection", "Pelvic infection", "pelvic infection", "infection pelvis", "infection pelvic", "PELVIS INFECTION", "Pelvic Infection", "pelvis; infection", "Pelvic Infections", "pelvic infections", "Infection, Pelvic", "infection; pelvic", "Infections, Pelvic", "Infection of pelvis", "pelvic infection (diagnosis)", "Infection of pelvis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pelvic Infection", "shortest_name_length": 16}
{"curie": "UMLS:C1263787", "names": ["Broad Ligament Neoplasm", "Neoplasm of broad ligament", "neoplasm of broad ligament", "Neoplasm of broad ligament (disorder)", "neoplasm of broad ligament (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplasm of broad ligament", "shortest_name_length": 23}
{"curie": "MONDO:0007199", "names": ["Blepharochalasis, Superior", "blepharochalasis, superior", "BLEPHAROCHALASIS, SUPERIOR"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blepharochalasis, superior", "shortest_name_length": 26}
{"curie": "MONDO:0001747", "names": ["tibial collateral ligament bursitis", "Tibial collateral ligament bursitis", "bursitis of tibial collateral ligament", "bursitis of tibial collateral ligament (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tibial collateral ligament bursitis", "shortest_name_length": 35}
{"curie": "MONDO:0020531", "names": ["LCAD", "LCAD deficiency", "ACADL deficiency", "Long-chain acyl-CoA dehydrogenase deficiency", "long-chain acyl-CoA dehydrogenase deficiency", "Long chain acyl-CoA dehydrogenase deficiency", "Long-Chain Acyl-CoA Dehydrogenase Deficiency", "long chain acyl-CoA dehydrogenase deficiency", "acyl-CoA dehydrogenase, long-chain deficiency", "Acyl-CoA Dehydrogenase, Long-Chain Deficiency", "Acyl-Coa Dehydrogenase, Long-Chain, Deficiency of", "Long-Chain Acyl-Coenzyme A Dehydrogenase Deficiency", "Long-chain acyl-coenzyme A dehydrogenase deficiency", "Long chain acyl-coenzyme A dehydrogenase deficiency", "long-chain acyl-Coenzyme A dehydrogenase deficiency", "LCAD - Long chain acyl-CoA dehydrogenase deficiency", "inborn error of long-chain-acyl-CoA dehydrogenase activity", "inborn long-chain-acyl-CoA dehydrogenase activity disorder", "Long chain acyl-coenzyme A dehydrogenase deficiency (disorder)", "rare inborn error of long-chain-acyl-CoA dehydrogenase activity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "long chain acyl-CoA dehydrogenase deficiency", "shortest_name_length": 4}
{"curie": "UMLS:C5205579", "names": ["Prostate Acinar Adenocarcinoma, Microcystic Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Acinar Adenocarcinoma, Microcystic Variant", "shortest_name_length": 51}
{"curie": "UMLS:C1334383", "names": ["Leiomyosarcoma NCI Grade 2", "Leiomyosarcoma NCI Grade II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leiomyosarcoma NCI Grade 2", "shortest_name_length": 26}
{"curie": "UMLS:C1443971", "names": ["chronic esophagitis", "Chronic esophagitis", "Chronic Esophagitis", "Chronic oesophagitis", "Chronic esophagitis (disorder)", "chronic esophagitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic esophagitis", "shortest_name_length": 19}
{"curie": "MONDO:0019651", "names": ["idiopathic steroid-sensitive nephrotic syndrome with diffuse mesangial proliferation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic steroid-sensitive nephrotic syndrome with diffuse mesangial proliferation", "shortest_name_length": 84}
{"curie": "MONDO:0400004", "names": ["phrynoderma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phrynoderma", "shortest_name_length": 11}
{"curie": "MONDO:0031213", "names": ["restrictive dermopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "restrictive dermopathy", "shortest_name_length": 22}
{"curie": "MONDO:0044816", "names": ["genetic torsion dystonia", "Genetic torsion dystonia", "dystonia idiopathic familial", "idiopathic familial dystonia", "familial Idiopathic dystonia", "Idiopathic familial dystonia", "Idiopathic Familial Dystonia", "Familial Idiopathic Dystonia", "Idiopathic Familial Dystonias", "Familial Dystonia, Idiopathic", "Dystonia, Idiopathic Familial", "idiopathic; dystonia, familial", "dystonia; idiopathic, familial", "Familial Dystonias, Idiopathic", "Dystonias, Idiopathic Familial", "familial idiopathic torsion dystonia", "hereditary idiopathic torsion dystonia", "Idiopathic familial dystonia (disorder)", "idiopathic familial dystonia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial idiopathic torsion dystonia", "shortest_name_length": 24}
{"curie": "MONDO:0012655", "names": ["EJM4", "juvenile myoclonic epilepsy 4", "myoclonic epilepsy, juvenile, 4", "MYOCLONIC EPILEPSY, JUVENILE, SUSCEPTIBILITY TO, 4", "myoclonic epilepsy, juvenile, susceptibility to, 4", "MYOCLONIC EPILEPSY, JUVENILE, SUSCEPTIBILITY TO, 4 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myoclonic epilepsy, juvenile, susceptibility to, 4", "shortest_name_length": 4}
{"curie": "MONDO:0021811", "names": ["soroche", "Soroche", "altitude anoxia", "ACOSTA SYNDROME", "acosta's disease", "Acosta's disease", "Mountain sickness", "altitude sickness", "acute mountain sickness", "Acute mountain sickness", "Mountain sickness acute", "MOUNTAIN SICKNESS, ACUTE", "high altitude cerebral edema", "high altitude pulmonary edema", "Acute mountain sickness (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute mountain sickness", "shortest_name_length": 7}
{"curie": "UMLS:C0334267", "names": ["Urothelial carcinoma in situ", "Transitional Carcinoma in situ", "Transitional Cell Carcinoma in situ", "Transitional cell carcinoma in situ", "Transitional cell carcinoma in-situ", "Stage 0 Transitional Cell Carcinoma", "transitional cell carcinoma in situ", "transitional cell carcinoma in situ (diagnosis)", "Transitional cell carcinoma in situ (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transitional cell carcinoma in situ", "shortest_name_length": 28}
{"curie": "UMLS:C5205936", "names": ["Extrarenal Rhabdoid Tumor of the Prostate", "Extrarenal Malignant Rhabdoid Tumor of the Prostate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extrarenal Rhabdoid Tumor of the Prostate", "shortest_name_length": 41}
{"curie": "MONDO:0003621", "names": ["small intestinal VIPoma", "Small Intestinal VIPoma", "Small Intestinal VIP-Producing NET", "small intestinal VIP-producing NET", "small intestinal VIP producing tumor", "small intestinal VIP Producing tumor", "small intestinal VIP Producing tumour", "small intestinal VIP-producing neuroendocrine tumor", "Small Intestinal VIP-Producing Neuroendocrine Tumor", "Small Intestinal Vasoactive Intestinal Peptide Producing Tumor", "small intestinal vasoactive intestinal peptide producing tumor", "small intestinal vasoactive intestinal peptide producing tumour"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small intestinal vasoactive intestinal peptide producing tumor", "shortest_name_length": 23}
{"curie": "MONDO:0019558", "names": ["DLE", "dle", "lupus", "lupus discoid", "discoid lupus", "DISCOID LUPUS", "Discoid lupus", "LUPUS DISCOID", "Lupus discoid", "discoid; lupus", "lupus; discoid", "Discoid lupus rash", "Lupus erythematosus discoid", "DISCOID LUPUS ERYTHEMATOSIS", "Discoid Lupus Erythematosus", "LUPUS ERYTHEMATOSUS DISCOID", "discoid lupus erythematosis", "Lupus erythematosis discoid", "discoid lupus erythematosus", "LUPUS ERYTHEMATOSIS DISCOID", "Discoid lupus erythematosus", "lupus erythematosus discoid", "Discoid lupus erythematosis", "LUPUS ERYTHEMATOSUS, DISCOID", "Lupus erythematosus, discoid", "Lupus Erythematosus, Discoid", "Lupus erythematosus discoides", "LE - Discoid lupus erythematosus", "discoid lupus erythematosus (DLE)", "DLE - Discoid lupus erythematosus", "Chronic discoid lupus erythematosus", "Chronic cutaneous lupus erythematosus", "Lupus Erythematosus, Chronic Cutaneous", "Discoid lupus erythematosus (disorder)", "Lupus Erythematosus, Cutaneous, Chronic", "lupus erythematosus discoid (diagnosis)", "CDLE - Chronic discoid lupus erythematosus", "Chronic discoid lupus erythematosus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "discoid lupus erythematosus", "shortest_name_length": 3}
{"curie": "UMLS:C4528746", "names": ["Refractory Extranodal Diffuse Large B-cell Lymphoma", "Refractory Extranodal Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Extranodal Diffuse Large B-cell Lymphoma", "shortest_name_length": 51}
{"curie": "UMLS:C4521798", "names": ["Stage IIA Gastric (Stomach) Cancer", "Clinical Stage IIA Gastric Cancer AJCC v8", "Clinical Stage IIA Gastric Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage IIA Gastric Cancer AJCC v8", "shortest_name_length": 34}
{"curie": "UMLS:C0033958", "names": ["brief psychotic disorder", "Brief reactive psychosis", "PSYCHOTIC DISORDER BRIEF", "Brief psychotic disorder", "Brief Reactive Psychosis", "Brief Reactive Psychoses", "brief reactive psychosis", "psychotic disorder brief", "Brief Psychotic Disorder", "Reactive Psychosis, Brief", "Psychoses, Brief Reactive", "Psychosis, Brief Reactive", "Reactive Psychoses, Brief", "Brief situational psychosis", "Brief reactive psychosis NOS", "Situational psychosis, brief", "Brief reactive psychosis (disorder)", "brief psychotic disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Psychosis, Brief Reactive", "shortest_name_length": 24}
{"curie": "UMLS:C0178298", "names": ["Skin and subcutaneous tissue disease", "skin and subcutaneous tissue disorder", "Skin and subcutaneous tissue disorders", "Skin and Subcutaneous Tissue Disorders", "Disorder of skin and subcutaneous tissue", "Disorder of skin and/or subcutaneous tissue", "DISEASES OF THE SKIN AND SUBCUTANEOUS TISSUE", "Disease of skin and subcutaneous tissue, NOS", "Diseases of the skin and subcutaneous tissue", "DISEASES OF THE SKIN AND SUBCUTANEOUS TISSUES", "Disorder of the dermis and subcutaneous tissue", "Unspecified disorder of skin and subcutaneous tissue", "Disorder of skin and subcutaneous tissue (diagnosis)", "Disorder of skin and subcutaneous tissue, unspecified", "Disorder of skin and/or subcutaneous tissue (disorder)", "Diseases of the skin and subcutaneous tissue (L00-L99)", "Disorder of the skin and subcutaneous tissue, unspecified", "DISEASES OF THE SKIN AND SUBCUTANEOUS TISSUES: GENERAL TERMS", "DISEASES OF THE SKIN AND SUBCUTANEOUS TISSUES: GENERAL TERMS AND HISTOLOGIC TYPES", "DISEASES OF THE SKIN AND SUBCUTANEOUS TISSUES: GENERAL TERMS, HISTOLOGIC TYPES AND INFECTIONS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin and subcutaneous tissue disorders", "shortest_name_length": 36}
{"curie": "UMLS:C5420023", "names": ["Sinonasal HPV-Related Carcinoma with Adenoid Cystic-Like Features", "Sinonasal Tract HPV-Related Carcinoma with Adenoid Cystic-Like Features", "Sinonasal Human Papillomavirus-Related Carcinoma with Adenoid Cystic-Like Features", "Sinonasal Tract Human Papillomavirus-Related Carcinoma with Adenoid Cystic-Like Features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Human Papillomavirus-Related Carcinoma with Adenoid Cystic-Like Features", "shortest_name_length": 65}
{"curie": "MONDO:0008322", "names": ["PSACH", "SED syndrome", "PSEUDOACHONDROPLASIA", "pseudoachondroplasia", "Pseudoachondroplasia", "pseudoachondroplastic dysplasia", "Pseudoachondroplastic dysplasia", "PSEUDOACHONDROPLASTIC DYSPLASIA", "pseudoachondroplasia (diagnosis)", "Pseudoachondroplastic spondyloepiphyseal dysplasia", "Spondyloepiphyseal Dysplasia, Pseudoachondroplastic", "SPONDYLOEPIPHYSEAL DYSPLASIA, PSEUDOACHONDROPLASTIC", "spondyloepiphyseal dysplasia, PSEUDOACHONDROPLASTIC", "spondyloepiphyseal dysplasia, Pseudoachondroplastic", "Pseudoachondroplastic Spondyloepiphyseal Dysplasia Syndrome", "Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome", "Pseudo-achondroplastic spondyloepiphyseal dysplasia syndrome", "Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudoachondroplasia", "shortest_name_length": 5}
{"curie": "UMLS:C3897450", "names": ["Subcapsular Hematoma", "Subcapsular renal hematoma", "Subcapsular Renal Hematoma", "Subcapsular renal haematoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subcapsular renal hematoma", "shortest_name_length": 20}
{"curie": "MONDO:0023679", "names": ["Hematidrosis", "Hematohidrosis", "hematohidrosis", "Haematohidrosis", "Hematohidrosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hematohidrosis", "shortest_name_length": 12}
{"curie": "UMLS:C5556663", "names": ["HPVA Cervical Adenocarcinoma In Situ", "HPV-Related Cervical Adenocarcinoma In Situ", "HPV-Associated Cervical Adenocarcinoma In Situ", "Human Papillomavirus-Related Cervical Adenocarcinoma In Situ", "Human Papillomavirus-Associated Cervical Adenocarcinoma In Situ"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Human Papillomavirus-Related Cervical Adenocarcinoma In Situ", "shortest_name_length": 36}
{"curie": "UMLS:C4524708", "names": ["Gastroesophageal Junction Adenocarcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastroesophageal Junction Adenocarcinoma by AJCC v8 Stage", "shortest_name_length": 57}
{"curie": "MONDO:0008499", "names": ["STRATTON-PARKER SYNDROME", "Stratton Parker syndrome", "Stratton-Parker Syndrome", "STRATTON-PARKER syndrome", "Stratton-Parker syndrome", "short stature wormian bones dextrocardia", "short stature-wormian bones-dextrocardia syndrome", "Short stature-wormian bones-dextrocardia syndrome", "Short stature, wormian bones, dextrocardia syndrome", "Short stature, wormian bones, dextrocardia syndrome (disorder)", "GROWTH HORMONE DEFICIENCY WITH WORMIAN BONES, CARDIAC ANOMALY, AND BRACHYCAMPTODACTYLY", "Growth Hormone Deficiency with Wormian Bones, Cardiac Anomaly, and Brachycamptodactyly", "Growth hormone deficiency with Wormian bones, Cardiac anomaly, and Brachycamptodactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short stature-wormian bones-dextrocardia syndrome", "shortest_name_length": 24}
{"curie": "MONDO:0004981", "names": ["AF", "af", "AFib", "afib", "a fib", "A fib", "A-fib", "ATRIAL FIBRILLATION", "FIBRILLATION ATRIAL", "Fibrillation;atrial", "Fibrillation atrial", "Atrial fibrillation", "atrial fibrillation", "Atrial Fibrillation", "Fibrillation, Atrial", "atrial fibrillations", "Atrial Fibrillations", "atrium; fibrillation", "Fibrillations, Atrial", "Auricular fibrillation", "AURICULAR FIBRILLATION", "Auricular Fibrillation", "auricular fibrillation", "Auricular Fibrillations", "auricular fibrillations", "auricular; fibrillation", "Fibrillation, Auricular", "AF - Atrial fibrillation", "atrial fibrillation (AF)", "Fibrillations, Auricular", "atrial fibrillation (disease)", "Atrial fibrillation (disorder)", "atrial fibrillation (diagnosis)", "fibrillation; atrial or auricular", "Quivering upper heart chambers resulting in irregular heartbeat"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial fibrillation", "shortest_name_length": 2}
{"curie": "MONDO:0019451", "names": ["CNL", "neutrophilic leukemia", "Neutrophilic Leukemia", "Neutrophilic leukemia", "Neutrophilic leukaemia", "[M]Neutrophilic leukemia", "[M]Neutrophilic leukaemia", "chronic neutrophilic leukemia", "Chronic neutrophilic leukemia", "Chronic Neutrophilic Leukemia", "leukemia chronic neutrophilic", "Chronic Neutrophilic Leukemias", "Chronic neutrophilic leukaemia", "Neutrophilic Leukemia, Chronic", "Leukemia, Chronic Neutrophilic", "Neutrophilic Leukemias, Chronic", "Leukemias, Chronic Neutrophilic", "Leukemia, Neutrophilic, Chronic", "Neutrophilic leukemia (disorder)", "Chronic neutrophilic leukemia (disorder)", "chronic neutrophilic leukemia (diagnosis)", "Chronic neutrophilic leukemia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic neutrophilic leukemia", "shortest_name_length": 3}
{"curie": "MONDO:0009150", "names": ["HEDH syndrome", "HEDH SYNDROME", "another syndrome", "ANOTHER syndrome", "hypohidrotic ectodermal dysplasia with hypothyroidism", "hypohidrotic ectodermal dysplasia - hypothyroidism - ciliary dyskinesia", "hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome", "ectodermal dysplasia hypohidrotic with hypothyroidism and ciliary dyskinesia", "hypohidrotic ectodermal dysplasia with hypothyroidism and ciliary dyskinesia", "Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome", "Hypohidrotic ectodermal dysplasia, hypothyroidism, ciliary dyskinesia syndrome", "Ectodermal Dysplasia, Hypohidrotic, with Hypothyroidism and Ciliary Dyskinesia", "ectodermal dysplasia, hypohidrotic, with hypothyroidism and ciliary dyskinesia", "ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH HYPOTHYROIDISM AND CILIARY DYSKINESIA", "Alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy and respiratory tract infections", "ANOTHER - Alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy and respiratory tract infections", "Alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy and respiratory tract infections (disorder)", "ANOTHER (alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy, respiratory tract infection) syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0013599", "names": ["CANDF7", "IMD31C", "Immunodeficiency 31C", "IMMUNODEFICIENCY 31C", "immunodeficiency 31C", "familial candidiasis 7", "Familial Candidiasis 7", "candidiasis familial, 7", "CANDIDIASIS, FAMILIAL, 7", "candidiasis, familial, 7", "immunodeficiency type 31C", "STAT1-Associated Immunodeficiency", "autosomal dominant immunodeficiency 31C", "familial chronic mucocutaneous, autosomal dominant", "autosomal dominant chronic mucocutaneous familial candidiasis", "candidiasis familial chronic mucocutaneous, autosomal dominant", "candidiasis, familial chronic mucocutaneous, autosomal dominant", "CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL DOMINANT", "immunodeficiency 31C, chronic mucocutaneous candidiasis, autosomal dominant", "autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome", "autoimmune enteropathy and endocrinopathy - susceptibility to chronic infections syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune enteropathy and endocrinopathy - susceptibility to chronic infections syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0014388", "names": ["OFC14", "orofacial cleft 14", "OROFACIAL CLEFT 14", "familial median cleft of the upper and lower lips"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial median cleft of the upper and lower lips", "shortest_name_length": 5}
{"curie": "MONDO:0019147", "names": ["Myiases", "MYIASIS", "Myiasis", "myiasis", "myiases", "Fly Strike", "Fly Strikes", "Myiasis, NOS", "MAGGOT INFECTION", "maggot infestation", "MAGGOT INFESTATION", "Maggot Infestation", "Maggot infestation", "infestation maggot", "Maggot Infestations", "Infestation, Maggot", "infestation; maggots", "Myiasis, unspecified", "myiasis, unspecified", "Infestations, Maggot", "maggots; infestation", "Fly larva infestation", "infestation by maggots", "Infestation by maggots", "infestation; fly larvae", "fly larvae; infestation", "Infestation by fly larvae", "infestation by fly larvae", "Infestation caused by maggots", "infestation by larva of flies", "Infestation by fly larvae, NOS", "Infestation caused by fly larvae", "Myiasis - fly larvae infestation", "infestation by maggots (diagnosis)", "infestation by fly larvae (diagnosis)", "Infestation caused by fly larvae (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myiasis", "shortest_name_length": 7}
{"curie": "UMLS:C0340652", "names": ["artery injury", "injury; artery", "artery; injury", "arterial injury", "Arterial injury", "artery injuries", "arteries injury", "Arterial Injury", "Injury of artery", "arterial injuries", "Arterial injury, NOS", "Injury of artery, NOS", "Arterial injury (diagnosis)", "Injury of artery (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arterial Injury", "shortest_name_length": 13}
{"curie": "MONDO:0006629", "names": ["hip osteoarthritis", "Hip osteoarthritis", "Hip Osteoarthritis", "osteoarthritis, hip", "Osteoarthritis, Hip", "Osteoarthritis of hip"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteoarthritis, hip", "shortest_name_length": 18}
{"curie": "MONDO:0010396", "names": ["CDD", "DEE2", "CDKL5", "EIEE2", "ISSX2", "CDKL5 Disorder", "CDKL5-deficiency disorder", "CDKL5 deficiency disorder", "X-linked infantile spasm syndrome 2", "INFANTILE SPASM SYNDROME, X-LINKED 2", "infantile spasm syndrome, X-linked 2", "Infantile Spasm Syndrome, X-Linked 2", "Rett Syndrome, Atypical, Cdkl5-Related", "CDKL5-related epileptic encephalopathy", "Cyclin-dependent kinase-like 5 deficiency", "early infantile epileptic encephalopathy 2", "Early Infantile Epileptic Encephalopathy 2", "Epileptic Encephalopathy, Early Infantile, 2", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 2", "epileptic encephalopathy, early infantile, 2", "developmental and epileptic encephalopathy 2", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2", "Developmental and Epileptic Encephalopathy 2", "Rett Syndrome, Variant, With Infantile Spasms", "developmental and epileptic encephalopathy, 2", "CDKL5 early infantile epileptic encephalopathy", "CDKL5 (cyclin-dependent kinase-like 5) deficiency", "epileptic encephalopathy, early infantile, type 2", "Cyclin-Dependent Kinase-Like 5 Deficiency Disorder", "cyclin dependent kinase-like 5 deficiency disorder", "Cyclin-dependent kinase-like 5 deficiency (disorder)", "cyclin dependent kinase-like 5 deficiency disorder (diagnosis)", "developmental and epileptic encephalopathy 2, X-linked dominant", "early infantile epileptic encephalopathy caused by mutation in CDKL5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 2", "shortest_name_length": 3}
{"curie": "MONDO:0017793", "names": ["marfanoid habitus-inguinal hernia-advanced bone age syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "marfanoid habitus-inguinal hernia-advanced bone age syndrome", "shortest_name_length": 60}
{"curie": "MONDO:0001644", "names": ["Post-Streptococcal Glomerulonephritis", "post-streptococcal glomerulonephritis", "acute proliferative glomerulonephritis", "Acute proliferative glomerulonephritis", "proliferative glomerulonephritis acute", "Acute Proliferative Glomerulonephritis", "proliferative glomerulonephritis, acute", "PGN - Acute proliferative glomerulonephritis", "Acute proliferative glomerulonephritis (disorder)", "acute proliferative glomerulonephritis (diagnosis)", "acute glomerulonephritis with lesion of proliferative glomerulonephritis", "Acute glomerulonephritis with lesion of proliferative glomerulonephritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute proliferative glomerulonephritis", "shortest_name_length": 37}
{"curie": "MONDO:8000013", "names": ["NCPH", "NCPH1", "portal hypertension, noncirrhotic", "PORTAL HYPERTENSION, NONCIRRHOTIC, 1", "portal hypertension, noncirrhotic, 1", "portal hypertension, noncirrhotic; NCPH"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "portal hypertension, noncirrhotic, 1", "shortest_name_length": 4}
{"curie": "UMLS:C5206868", "names": ["PSRSTT", "Testicular Signet-Ring Stromal Tumor", "Testicular Signet Ring Stromal Tumor", "Primary Signet Ring Stromal Tumor of the Testis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular Signet Ring Stromal Tumor", "shortest_name_length": 6}
{"curie": "MONDO:0006359", "names": ["PEComa", "pecoma", "PEComas", "pecomas", "Perivascular epithelioid tumour", "Perivascular epithelial cell tumor", "perivascular epithelioid cell tumor", "Perivascular Epithelioid Cell Tumor", "Perivascular epithelioid cell tumor", "Perivascular epithelial cell tumour", "Perivascular Epithelioid Cell Tumors", "Perivascular epithelioid cell tumour", "Perivascular epithelioid cell neoplasm", "Perivascular Epithelioid Cell Neoplasm", "Perivascular Epithelioid Cell Neoplasms", "Neoplasms, Perivascular Epithelioid Cell", "Tumor with Perivascular Epithelioid Cell Differentiation", "tumor with perivascular epithelioid cell differentiation", "neoplasm with Perivascular epithelioid cell differentiation", "neoplasm with perivascular epithelioid cell differentiation", "Neoplasm with Perivascular Epithelioid Cell Differentiation", "Perivascular epithelioid cell tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplasm with perivascular epithelioid cell differentiation", "shortest_name_length": 6}
{"curie": "UMLS:C5205655", "names": ["Locally Advanced Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Liposarcoma", "shortest_name_length": 28}
{"curie": "MONDO:0000133", "names": ["CIID", "ICF syndrome", "IMMUNODEFICIENCY SYNDROME, VARIABLE", "Immunodeficiency syndrome, variable", "centromeric instability-immunodeficiency syndrome", "CENTROMERIC INSTABILITY, IMMUNODEFICIENCY SYNDROME", "Centromeric instability, immunodeficiency syndrome", "immunodeficiency-centromeric instability-facial anomalies", "immunodeficiency-centromeric instability-facial anomalies syndrome", "Immunodeficiency-centromeric instability-facial anomalies syndrome", "Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency", "centromeric instability of chromosomes 1, 9, and 16 and immunodeficiency", "immunodeficiency-centromeric instability-facial anomalies (ICF) syndrome", "Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency (disorder)", "immunodeficiency-centromeric heterochromatin instability-facial anomalies syndrome", "centromeric instability of chromosomes 1, 9, and 16 and immunodeficiency (diagnosis)", "IMMUNE DEFICIENCY, VARIABLE, WITH CENTROMERIC INSTABILITY OF CHROMOSOMES 1, 9, AND 16"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency-centromeric instability-facial anomalies syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C1262036", "names": ["Ocular toxicity", "ocular toxicity", "Ocular Toxicity", "Toxicity, Ocular"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ocular Toxicity", "shortest_name_length": 15}
{"curie": "UMLS:C5230986", "names": ["Plaque-like CD34 positive dermal fibroma", "Plaque-Like CD34-Positive Dermal Fibroma", "Medallion-Like Dermal Dendrocyte Hamartoma", "Plaque-like CD34 positive dermal fibroma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Plaque-like CD34 positive dermal fibroma", "shortest_name_length": 40}
{"curie": "MONDO:0044724", "names": ["MGA9", "MGCA9", "3-methylglutaconic aciduria type 9", "3-Methylglutaconic aciduria, type 9", "3-methylglutaconic acuduria type IX", "3-METHYLGLUTACONIC ACIDURIA, TYPE IX", "3-METHYLGLUTACONIC aciduria, type IX", "3-@METHYLGLUTACONIC ACIDURIA, TYPE IX", "3-methylglutaconic acuduria type IX, MGCA9", "3-methylglutaconic aciduria type 9 (disorder)", "3-methylglutaconic aciduria-epilepsy-spasticity-severe intellectual disability syndrome", "3-methylglutaconic aciduria, epilepsy, spasticity, severe intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "3-methylglutaconic aciduria type 9", "shortest_name_length": 4}
{"curie": "UMLS:C5238497", "names": ["Adnexal Secretory Carcinoma", "Mammary-Type Secretory Carcinoma of the Skin", "Primary Cutaneous Mammary Analogue Secretory Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adnexal Secretory Carcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C3898658", "names": ["TYPE 1 MYOCARDIAL INFARCTION", "Type 1 myocardial infarction", "Joint Task Force Type 1 Myocardial Infarction", "Joint ESC/ACCF/AHA/WHF Task Force Type 1 Myocardial Infarction", "Myocardial infarction due to atherothrombotic coronary artery disease", "myocardial infarction due to atherothrombotic coronary artery disease", "Myocardial infarction due to atherothrombotic coronary artery disease (disorder)", "myocardial infarction due to atherothrombotic coronary artery disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myocardial infarction due to atherothrombotic coronary artery disease", "shortest_name_length": 28}
{"curie": "MONDO:0016744", "names": ["primary melanocytic tumor of CNS", "primary melanocytic lesion of CNS", "primary melanocytic tumor of central nervous system", "primary melanocytic lesion of central nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary melanocytic tumor of central nervous system", "shortest_name_length": 32}
{"curie": "UMLS:C4086315", "names": ["First Trimester Antepartum Hemorrhage", "Antepartum Hemorrhage, First Trimester"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "First Trimester Antepartum Hemorrhage", "shortest_name_length": 37}
{"curie": "MONDO:0045014", "names": ["tetrahydrobiopterin metabolism disease", "Disorder of tetrahydrobiopterin metabolism", "disorder of tetrahydrobiopterin metabolism", "tetrahydrobiopterin metabolic process disease", "disorder of tetrahydrobiopterin metabolic process", "Disorder of tetrahydrobiopterin metabolism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tetrahydrobiopterin metabolic process disease", "shortest_name_length": 38}
{"curie": "MONDO:0004283", "names": ["vulvar clear cell hidradenocarcinoma", "Vulvar Clear Cell Hidradenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar clear cell hidradenocarcinoma", "shortest_name_length": 36}
{"curie": "UMLS:C0334563", "names": ["Complex odontoma", "Complex odontome", "Complex Odontoma", "complex; odontoma", "odontoma; complex", "Complex odontoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Complex odontoma", "shortest_name_length": 16}
{"curie": "MONDO:0016893", "names": ["partial monosomy of chromosome 11p", "partial deletion of chromosome 11p", "partial deletion of the short arm of chromosome 11", "partial monosomy of the short arm of chromosome 11", "partial deletion of the short arm of chromosome type 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of the short arm of chromosome 11", "shortest_name_length": 34}
{"curie": "MONDO:0100338", "names": ["UTI", "urinary tract infection", "Urinary Tract Infections", "urinary tract infection (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urinary tract infection", "shortest_name_length": 3}
{"curie": "UMLS:C4683573", "names": ["Lugano Classification Stage IV Adult Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage IV Adult Lymphoma AJCC v8", "shortest_name_length": 53}
{"curie": "MONDO:0100410", "names": ["AML, t(16;21)(p11;q22)", "AML, t(16;21)(p11.2;q22.2)", "acute myeloid leukemia, t(16;21)(p11;q22)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, t(16;21)(p11;q22)", "shortest_name_length": 22}
{"curie": "UMLS:C3536740", "names": ["Cervical Meningomyelocele", "Cervical Myelomeningocele", "cervical meningomyelocele", "Cervical meningomyelocele", "Cervical meningomyelocele (disorder)", "cervical meningomyelocele (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical meningomyelocele", "shortest_name_length": 25}
{"curie": "UMLS:C4521743", "names": ["IIA", "Stage IIA Esophageal Squamous Cell Cancer", "Pathologic Stage IIA Esophageal Squamous Cell Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IIA Esophageal Squamous Cell Carcinoma AJCC v8", "shortest_name_length": 3}
{"curie": "MONDO:0033853", "names": ["congenital cataract-severe neonatal hepatopathy-global developmental delay syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital cataract-severe neonatal hepatopathy-global developmental delay syndrome", "shortest_name_length": 83}
{"curie": "UMLS:C5670679", "names": ["Stage IIB Cervical Cancer FIGO 2009", "Stage IIB Cervical Carcinoma FIGO 2009"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Cervical Cancer FIGO 2009", "shortest_name_length": 35}
{"curie": "MONDO:0012344", "names": ["Ad11", "AD11", "Alzheimer disease-11", "ALZHEIMER DISEASE 11", "Alzheimer Disease 11", "Alzheimer disease 11", "Alzheimer's disease 11", "Alzheimer disease type 11", "Alzheimer's disease type 11", "Alzheimer disease, familial, 11", "ALZHEIMER DISEASE, FAMILIAL, 11", "Alzheimer Disease, Familial, 11", "Alzheimer's disease 11, late onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alzheimer disease 11", "shortest_name_length": 4}
{"curie": "UMLS:C4054944", "names": ["FSGS Perihilar Variant", "Focal Segmental Glomerulosclerosis Perihilar Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Focal Segmental Glomerulosclerosis Perihilar Variant", "shortest_name_length": 22}
{"curie": "MONDO:0014219", "names": ["AAMR", "GMPPA-CDG", "Intellectual disability-alacrima-achalasia syndrome", "alacrima, achalasia, and mental retardation syndrome", "ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME", "Intellectual disability, alacrima, achalasia syndrome", "intellectual disabilities alacrima, achalasia syndrome", "alacrima, achalasia, and intellectual disability syndrome", "Intellectual disability, alacrima, achalasia syndrome (disorder)", "Intellectual disability, alacrima, achalasia syndrome (diagnosis)", "alacrima, achalasia, and impaired intellectual development syndrome", "ALACRIMA, ACHALASIA, AND IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alacrima, achalasia, and intellectual disability syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C5420355", "names": ["Parotid Gland Diffuse Large B-Cell Lymphoma", "Primary Parotid Gland Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parotid Gland Diffuse Large B-Cell Lymphoma", "shortest_name_length": 43}
{"curie": "MONDO:0040678", "names": ["Infiltrating Urothelial Carcinoma", "infiltrating urothelial carcinoma", "infiltrating transitional cell carcinoma of the urinary tract", "Infiltrating Transitional Cell Carcinoma of the Urinary Tract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infiltrating urothelial carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0009889", "names": ["PKD4", "PKHD1", "Arpkd", "Pkhd1", "arpkd", "ARPKD", "arpkds", "AR-PKD", "PKD3, FORMERLY", "POLYCYSTIC KIDNEY DISEASE INFANT", "disease infants kidney polycystic", "Polycystic kidney, infantile type", "polycystic; kidney, infantile type", "Infantile polycystic kidney disease", "Autosomal Recessive Polycystic Kidney", "cyst; kidney, multiple infantile type", "autosomal recessive polycystic kidney", "Polycystic kidney, autosomal recessive", "Polycystic Kidney, Autosomal Recessive", "POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1", "polycystic kidney and hepatic disease 1", "Polycystic Kidney and Hepatic Disease 1", "Kidney, Polycystic, Autosomal Recessive", "Polycystic kidney disease, infantile type", "polycystic kidney disease, infantile type", "Polycystic Kidney Disease, Infantile Type", "IPKD - Infantile polycystic kidney disease", "POLYCYSTIC KIDNEY DISEASE, INFANTILE, TYPE I", "polycystic kidney disease, infantile, type I", "Polycystic Kidney Disease, Infantile, Type 1", "Polycystic Kidney Disease, Infantile, Type I", "autosomal recessive polycystic kidney disease", "Autosomal recessive polycystic kidney disease", "Autosomal Recessive Polycystic Kidney Disease", "Polycystic Kidney Disease, Autosomal Recessive", "polycystic kidney disease, autosomal recessive", "POLYCYSTIC KIDNEY DISEASE, AUTOSOMAL RECESSIVE", "polycystic; degeneration, kidney, infantile type", "Polycystic kidney disease, infantile type (disorder)", "ARPKD - Autosomal recessive polycystic kidney disease", "Autosomal recessive infantile polycystic kidney disease", "autosomal recessive polycystic kidney disease (diagnosis)", "POLYCYSTIC KIDNEY DISEASE 4 WITH OR WITHOUT HEPATIC DISEASE", "Polycystic Kidney and Hepatic Disease 1 (Autosomal Recessive)", "POLYCYSTIC KIDNEY DISEASE 4 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive polycystic kidney disease", "shortest_name_length": 4}
{"curie": "UMLS:C0263984", "names": ["Polymyositis ossificans", "Polymyositis Ossificans", "ossificans; polymyositis", "Ossificans, Polymyositis", "polymyositis; ossificans", "Polymyositis ossificans (disorder)", "Myositis ossificans associated with dermato / polymyositis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Polymyositis Ossificans", "shortest_name_length": 23}
{"curie": "MONDO:0017482", "names": ["humeral agenesis/hypoplasia, unilateral", "humeral intercalary meromelia, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "humeral agenesis/hypoplasia, unilateral", "shortest_name_length": 39}
{"curie": "MONDO:0012749", "names": ["Mesomelic Dysplasia, Camera Type", "mesomelic dysplasia, camera type", "MESOMELIC DYSPLASIA, CAMERA TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mesomelic dysplasia, camera type", "shortest_name_length": 32}
{"curie": "MONDO:0032705", "names": ["NEDMEHM", "neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination", "NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, EPILEPSY, AND HYPOMYELINATION", "MTHFS-related developmental delay-microcephaly-short stature-epilepsy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination", "shortest_name_length": 7}
{"curie": "MONDO:0007465", "names": ["distichiasis-congenital heart defects-peripheral vascular anomalies syndrome", "DISTICHIASIS WITH CONGENITAL ANOMALIES OF THE HEART AND PERIPHERAL VASCULATURE", "Distichiasis with Congenital Anomalies of the Heart and Peripheral Vasculature", "distichiasis with congenital anomalies of the heart and peripheral vasculature"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distichiasis with congenital anomalies of the heart and peripheral vasculature", "shortest_name_length": 76}
{"curie": "MONDO:0010961", "names": ["PCI deficiency", "Proprotein Convertase 1 3 Deficiency", "PROPROTEIN CONVERTASE 1/3 DEFICIENCY", "proprotein convertase 1/3 deficiency", "obesity with impaired prohormone processing", "Obesity due to prohormone convertase I deficiency", "obesity due to prohormone convertase I deficiency", "Obesity due to prohormone convertase I deficiency (disorder)", "obesity and endocrinopathy due to impaired processing of prohormones", "Obesity and Endocrinopathy due to Impaired Processing of Prohormones", "OBESITY AND ENDOCRINOPATHY DUE TO IMPAIRED PROCESSING OF PROHORMONES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "obesity due to prohormone convertase I deficiency", "shortest_name_length": 14}
{"curie": "UMLS:C1334241", "names": ["Intracranial Lipoma", "Intracranial lipoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intracranial lipoma", "shortest_name_length": 19}
{"curie": "MONDO:0004529", "names": ["nonossifying fibromyxoma", "Nonossifying Fibromyxoma", "nonossifying fibromyxoid tumor", "Nonossifying Fibromyxoid Tumor", "non-ossifying fibromyxoid tumor", "nonossifying fibromyxoid neoplasm", "Nonossifying Fibromyxoid Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-ossifying fibromyxoid tumor", "shortest_name_length": 24}
{"curie": "MONDO:0016923", "names": ["Duplication of chromosome 3", "partial trisomy of chromosome 3", "Partial trisomy of chromosome 3", "partial duplication of chromosome 3", "Partial duplication of chromosome 3", "partial duplication of chromosome type 3", "Partial trisomy of chromosome 3 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of chromosome 3", "shortest_name_length": 27}
{"curie": "MONDO:0012073", "names": ["RPIAD", "ribose-5-P isomerase deficiency", "Ribose-5-P isomerase deficiency", "Deficiency of phosphoriboisomerase", "Deficiency of phosphopentosisomerase", "ribose 5-phosphate isomerase deficiency", "RIBOSE 5-PHOSPHATE ISOMERASE DEFICIENCY", "Ribose 5-Phosphate Isomerase Deficiency", "Deficiency of ribose-5-phosphate isomerase", "Deficiency of ribose-5-phosphate isomerase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ribose-5-P isomerase deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0030869", "names": ["SPGF50", "spermatogenic failure", "SPERMATOGENIC FAILURE 50", "spermatogenic failure 50", "spermatogenic failures 50"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failures 50", "shortest_name_length": 6}
{"curie": "MONDO:0005295", "names": ["Claudication", "syndrome; Charcot", "Charcot; syndrome", "Charcot's syndrome", "charcot's syndrome", "Angiosclerotic myasthenia", "CLAUDICATION INTERMITTENT", "intermittent claudication", "Intermittent claudication", "INTERMITTENT CLAUDICATION", "claudication intermittent", "Claudication intermittent", "Intermittent Claudication", "Claudication;intermittent", "Myasthenia angiosclerotica", "intermittent claudications", "claudication, intermittent", "Claudication, Intermittent", "Intermittent claudication NOS", "IC - Intermittent claudication", "intermittent vascular claudication", "Intermittent claudication (finding)", "intermittent claudication (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intermittent vascular claudication", "shortest_name_length": 12}
{"curie": "MONDO:0016520", "names": ["Klippel-Feil sequence", "Klippel-Feil malformation", "isolated Klippel-Feil syndrome", "congenital fused cervical segments", "nonsyndromic Klippel-Feil syndrome", "congenital cervical vertebral fusion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated Klippel-Feil syndrome", "shortest_name_length": 21}
{"curie": "MONDO:0016984", "names": ["ota nevus", "nevus ota", "Ota Nevus", "Otas Nevus", "Ota's Nevus", "Ota's nevus", "Ota's naevus", "nevus of ota", "Nevus, Ota's", "Nevus of Ota", "nevus of Ota", "Naevus of Ota", "naevus of ota", "Oculodermal melanocytosis", "oculodermal melanocytosis", "Oculodermal Melanocytosis", "Congenital melanosis bulbi", "Oculocutaneous melanocytic nevus", "Oculocutaneous Melanocytic Nevus", "oculocutaneous melanocytic Nevus", "Oculocutaneous melanocytic naevus", "Nevus fusoceruleus ophthalmomaxillaris", "Nevus fusoceruleus ophthalmomaxillasis", "Naevus fusoceruleus ophthalmomaxillaris", "Nevus fuscoceruleus ophthalmomaxillaris", "Naevus fusoceruleus ophthalmomaxillasis", "Nevus fuscocaeruleus ophthalmomaxillaris", "Naevus fuscoceruleus ophthalmomaxillaris", "Nevus fusculoceruleus ophthalmomaxillaris", "Naevus fuscocaeruleus ophthalmomaxillaris", "Primary acquired melanosis of conjunctiva", "Oculocutaneous melanocytic nevus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nevus of Ota", "shortest_name_length": 9}
{"curie": "MONDO:0021532", "names": ["prostate fibroma", "Prostate Fibroma", "prostate; fibroma", "fibroma; prostate", "Fibroma of Prostate", "fibroma of prostate", "Fibroma of prostate", "prostate gland fibroma", "Fibroma of the Prostate", "fibroma of the prostate", "Fibroma of prostate (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibroma of prostate", "shortest_name_length": 16}
{"curie": "MONDO:0021905", "names": ["apert like polydactyly syndrome", "apert-like polydactyly syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "apert-like polydactyly syndrome", "shortest_name_length": 31}
{"curie": "UMLS:C1332319", "names": ["Apocrine Sweat Gland Hamartoma", "Hamartoma of Apocrine Sweat Gland", "Hamartoma of the Apocrine Sweat Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Apocrine Sweat Gland Hamartoma", "shortest_name_length": 30}
{"curie": "MONDO:0018416", "names": ["SPG59", "autosomal recessive spastic paraplegia type 59"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive spastic paraplegia type 59", "shortest_name_length": 5}
{"curie": "UMLS:C5447390", "names": ["Non-Functioning Lung Carcinoid Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Functioning Lung Carcinoid Tumor", "shortest_name_length": 36}
{"curie": "MONDO:0021329", "names": ["cancer palate soft", "Soft Palate Cancer", "soft palate cancer", "Soft Palate Carcinoma", "soft palate carcinoma", "carcinoma of soft palate", "Carcinoma of Soft Palate", "Carcinoma of soft palate", "PALATE CANCER SOFT PALATE", "palate cancer soft palate", "Carcinoma of the Soft Palate", "carcinoma of the soft palate", "Carcinoma of soft palate (disorder)", "Carcinoma of soft palate (diagnosis)", "soft palate neoplasm malignant carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma of soft palate", "shortest_name_length": 18}
{"curie": "MONDO:0002730", "names": ["kidney neoplasm", "Kidney Neoplasm", "Pediatric Renal Tumor", "pediatric renal tumor", "childhood renal tumor", "Childhood Renal Tumor", "Childhood Kidney Tumor", "pediatric kidney tumor", "Pediatric Kidney Tumor", "childhood kidney tumor", "childhood kidney cancer", "Pediatric Renal Neoplasm", "Childhood Renal Neoplasm", "childhood renal neoplasm", "pediatric renal neoplasm", "pediatric kidney neoplasm", "childhood kidney neoplasm", "Pediatric Kidney Neoplasm", "Childhood Kidney Neoplasm", "kidney neoplasm of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood kidney neoplasm", "shortest_name_length": 15}
{"curie": "UMLS:C1710403", "names": ["Thymic NET G1", "Thymic Neuroendocrine Tumor G1", "Thymic Typical Carcinoid Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thymic Typical Carcinoid Tumor", "shortest_name_length": 13}
{"curie": "UMLS:C0746731", "names": ["Acute heart ischemia", "Acute heart ischaemia", "acute myocardial ischemia", "MYOCARDIAL ISCHEMIA ACUTE", "Acute myocardial ischemia", "Acute myocardial ischaemia", "Acute myocardial ischemia (disorder)", "acute myocardial ischemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute myocardial ischemia", "shortest_name_length": 20}
{"curie": "UMLS:C4054728", "names": ["Infant ALL without MLL Rearrangement", "Infant Acute Lymphoblastic Leukemia without MLL Gene Rearrangement", "Infant Acute Lymphoblastic Leukemia without KMT2A Gene Rearrangement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infant Acute Lymphoblastic Leukemia without MLL Gene Rearrangement", "shortest_name_length": 36}
{"curie": "MONDO:0023067", "names": ["African Kaposi sarcoma", "endemic Kaposi sarcoma", "African/endemic Kaposi sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endemic Kaposi sarcoma", "shortest_name_length": 22}
{"curie": "MONDO:0013137", "names": ["CACD2", "Progressive macular dystrophy", "MACULAR DYSTROPHY, PROGRESSIVE", "Macular Dystrophy, Progressive", "macular dystrophy, progressive", "Central Areolar Choroidal Dystrophy-2", "Choroidal Dystrophy, Central Areolar 2", "choroidal dystrophy, central areolar 2", "CHOROIDAL DYSTROPHY, CENTRAL AREOLAR 2", "CHOROIDAL DYSTROPHY, CENTRAL AREOLAR, 2", "PRPH2 central areolar choroidal dystrophy", "choroidal dystrophy, central areolar type 2", "central areolar choroidal dystrophy caused by mutation in PRPH2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choroidal dystrophy, central areolar 2", "shortest_name_length": 5}
{"curie": "MONDO:0014203", "names": ["CILD25", "primary ciliary dyskinesia 25", "ciliary dyskinesia, primary, 25", "CILIARY DYSKINESIA, PRIMARY, 25", "DNAAF4 primary ciliary dyskinesia", "primary ciliary dyskinesia type 25", "ciliary dyskinesia, primary, type 25", "primary ciliary dyskinesia caused by mutation in DNAAF4", "primary ciliary dyskinesia 25 with or without situs inversus", "ciliary dyskinesia, primary, 25, with or without situs inversus", "CILIARY DYSKINESIA, PRIMARY, 25, WITH OR WITHOUT SITUS INVERSUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia 25", "shortest_name_length": 6}
{"curie": "MONDO:0044925", "names": ["Mouth Cancer", "oral carcinoma", "carcinoma oral", "Oral carcinoma", "Mouth Carcinoma", "CARCINOMA MOUTH", "MOUTH CARCINOMA", "mouth carcinoma", "Mouth carcinoma", "carcinomas oral", "Carcinoma mouth", "MOUTH, CARCINOMA", "Carcinoma of mouth", "oral cavity cancer", "CARCINOMA OF MOUTH", "carcinoma of mouth", "Carcinoma of Mouth", "Oral Cavity Cancer", "carcinoma cavity oral", "oral cavity carcinoma", "Oral Cavity Carcinoma", "MOUTH CANCER, CARCINOMA", "Carcinoma of Oral Cavity", "carcinoma of oral cavity", "CARCINOMA OF ORAL CAVITY", "carcinoma of the oral cavity", "Carcinoma of the Oral Cavity", "carcinoma of oral cavity (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oral cavity carcinoma", "shortest_name_length": 12}
{"curie": "MONDO:0013994", "names": ["JBTS20", "JOUBERT SYNDROME 20", "Joubert syndrome 20", "TMEM231 Joubert syndrome", "Joubert syndrome type 20", "Joubert syndrome caused by mutation in TMEM231"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome 20", "shortest_name_length": 6}
{"curie": "UMLS:C2747866", "names": ["Trigeminocardiac Reflex", "Trigemino-cardiac reflex", "Reflex, Trigeminocardiac", "Trigemino-Cardiac Reflex", "Reflex, Trigemino-Cardiac", "Reflex, Trigemino Cardiac"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reflex, Trigeminocardiac", "shortest_name_length": 23}
{"curie": "UMLS:C1696086", "names": ["Prostatic Perforation", "Prostatic perforation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostatic perforation", "shortest_name_length": 21}
{"curie": "MONDO:0014245", "names": ["DBA12", "DIAMOND-BLACKFAN ANEMIA 12", "Diamond-Blackfan anemia 12", "RPL15 Diamond-Blackfan anemia", "Diamond-Blackfan Anemia type 12", "RPL15-related Diamond-Blackfan anemia", "Diamond-Blackfan anemia caused by mutation in RPL15"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diamond-Blackfan anemia 12", "shortest_name_length": 5}
{"curie": "MONDO:0001171", "names": ["SALPINGO OOPHORITIS ACUTE", "Acute salpingo-oophoritis", "acute salpingo-oophoritis", "salpingo-oophoritis; acute", "acute; salpingo-oophoritis", "salpingo-oophoritis, acute", "acute salpingitis and oophoritis", "Acute salpingitis and oophoritis", "Acute salpingo-oophoritis (disorder)", "acute salpingo-oophoritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute salpingo-oophoritis", "shortest_name_length": 25}
{"curie": "MONDO:0013227", "names": ["congenital PAI-1 deficiency", "Congenital PAI-1 deficiency", "hyperfibrinolysis due to Pai1 deficiency", "Hyperfibrinolysis Due To Pai1 Deficiency", "HYPERFIBRINOLYSIS DUE TO PAI1 DEFICIENCY", "Plasminogen Activator Inhibitor-1 Deficiency", "plasminogen activator INHIBITOR-1 deficiency", "PLASMINOGEN ACTIVATOR INHIBITOR-1 DEFICIENCY", "plasminogen activator inhibitor type 1 deficiency", "Congenital plasminogen activator inhibitor deficiency type 1", "Congenital plasminogen activator inhibitor type 1 deficiency", "congenital plasminogen activator inhibitor type 1 deficiency", "Congenital plasminogen activator inhibitor deficiency type 1 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital plasminogen activator inhibitor type 1 deficiency", "shortest_name_length": 27}
{"curie": "MONDO:0015062", "names": ["GNET", "Gastric NET", "gastric NET", "gastric NET G1/2", "gastric neuroendocrine tumor", "Gastric Neuroendocrine Tumor", "gastric well differentiated endocrine tumor", "Gastric Well Differentiated Endocrine Tumor", "Gastric Well Differentiated Endocrine Tumor/Carcinoma", "gastric well differentiated endocrine tumor/carcinoma", "well-differentiated neuroendocrine tumors of the stomach", "gastric neuroendocrine tumor, well differentiated, low or intermediate grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric neuroendocrine tumor, well differentiated, low or intermediate grade", "shortest_name_length": 4}
{"curie": "UMLS:C1275249", "names": ["Myoid Dermatofibrosarcoma Protuberans", "Dermatofibrosarcoma Protuberans with Myoid Differentiation", "Dermatofibrosarcoma protuberans with myoid differentiation", "Dermatofibrosarcoma protuberans with myoid differentiation (disorder)", "soft tissue dermatofibrosarcoma protuberans with myoid differentiation", "Dermatofibrosarcoma protuberans with myoid differentiation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dermatofibrosarcoma protuberans with myoid differentiation", "shortest_name_length": 37}
{"curie": "UMLS:C5206564", "names": ["Recurrent High Grade B-Cell Lymphoma with MYC, BCL2, and BCL6 Rearrangements", "Recurrent High-Grade B-Cell Lymphoma with MYC, BCL2, and BCL6 Rearrangements"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent High Grade B-Cell Lymphoma with MYC, BCL2, and BCL6 Rearrangements", "shortest_name_length": 76}
{"curie": "MONDO:0012860", "names": ["THPH4", "autosomal recessive PROC deficiency", "PROC Deficiency, Autosomal Recessive", "Proc deficiency, autosomal recessive", "PROC DEFICIENCY, AUTOSOMAL RECESSIVE", "autosomal recessive protein C deficiency", "protein C deficiency, autosomal recessive", "Protein C deficiency, autosomal recessive", "Protein C Deficiency, Autosomal Recessive", "PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE", "hereditary thrombophilia due to PC deficiency", "protein C deficiency, autosomal recessive (diagnosis)", "autosomal recessive thrombophilia due to protein C deficiency", "THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE", "thrombophilia due to protein C deficiency, autosomal recessive", "thrombophilia due to PROTEIN C deficiency, autosomal recessive", "hereditary thrombophilia due to congenital protein C deficiency", "thrombophilia 3 due to protein C deficiency, autosomal recessive", "autosomal recessive hereditary thrombophilia due to protein C deficiency", "Thrombophilia, Hereditary, Due To Protein C Deficiency, Autosomal Recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombophilia due to protein C deficiency, autosomal recessive", "shortest_name_length": 5}
{"curie": "MONDO:0024312", "names": ["cancer of short bone of upper limb"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cancer of short bone of upper limb", "shortest_name_length": 34}
{"curie": "MONDO:0013176", "names": ["WMS4", "WMSL", "WEILL-MARCHESANI SYNDROME 4", "Weill-Marchesani syndrome 4", "15q26.3 microdeletion syndrome", "WEILL-MARCHESANI-LIKE SYNDROME", "Weill-Marchesani-Like Syndrome", "Weill-Marchesani-like syndrome", "Weill-Marchesani 4 syndrome, recessive", "ichthyosis-short stature-brachydactyly-microspherophakia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Weill-Marchesani 4 syndrome, recessive", "shortest_name_length": 4}
{"curie": "MONDO:0030924", "names": ["PRAAS5", "proteasome-associated autoinflammatory syndrome 5", "PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "proteasome-associated autoinflammatory syndrome 5", "shortest_name_length": 6}
{"curie": "MONDO:0001463", "names": ["splenic flexure cancer", "Cancer of splenic flexure", "Ca splenic flexure - colon", "Splenic flexure colon cancer", "splenic flexure of colon cancer", "Malignant tumor of splenic flexure", "cancer of splenic flexure of colon", "malignant tumor of splenic flexure", "Malignant tumour of splenic flexure", "Malignant neoplasm of splenic flexure", "malignant neoplasm of splenic flexure", "malignant splenic flexure of colon neoplasm", "Malignant tumor of splenic flexure (disorder)", "malignant neoplasm of splenic flexure of colon", "Malignant neoplasm of splenic flexure of colon", "malignant neoplasm of splenic flexure (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "splenic flexure cancer", "shortest_name_length": 22}
{"curie": "MONDO:0004195", "names": ["Thymic Dysplasia", "thymic dysplasia", "dysplasia; thymic", "thymic; dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thymic dysplasia", "shortest_name_length": 16}
{"curie": "MONDO:0100280", "names": ["macroglobulinemia", "Macroglobulinemia", "macroglobulinaemia", "Macroglobulinaemia", "Macroglobulinemia NOS", "Macroglobulinaemia NOS", "Waldenstrom's syndrome", "Primary macroglobulinemia", "Primary Macroglobulinemia", "Macroglobulinemia, Primary", "Primary macroglobulinaemia", "lymphoplasmacytic lymphoma", "Lymphoplasmacytoid Lymphoma", "lymphoplasmacytoid lymphoma", "Macroglobulinemia (disorder)", "Lymphoplasmacytoid Lymphomas", "Lymphoma, Lymphoplasmacytoid", "Waldenstrom Macroglobulinemia", "Waldenström Macroglobulinemia", "Lymphomas, Lymphoplasmacytoid", "waldenstrom macroglobulinemia", "Waldenström macroglobulinemia", "Waldenstrom macroglobulinemia", "macroglobulinemia waldenstrom", "waldenstroms macroglobulinemia", "macroglobulinemia waldenstroms", "Waldenstroms Macroglobulinemia", "Waldenström macroglobulinaemia", "MACROGLOBULINEMIA, WALDENSTROM", "Waldenstrom macroglobulinaemia", "Waldenström; macroglobulinemia", "Waldenstrom Macroglobulinaemia", "Macroglobulinemia, Waldenstrom", "macroglobulinemia; Waldenström", "WALDENSTROMS MACROGLOBULINEMIA", "plasmacytoma, macroglobulinemia", "macroglobulinemia waldenstrom's", "Waldenstrom's Macroglobulinemia", "waldenstrom's macroglobulinemia", "Waldenstrom's macroglobulinemia", "Waldenstroms Macroglobulinaemia", "Waldenström's macroglobulinemia", "Macroglobulinemia, Waldenstrom's", "macroglobulinemia of Waldenstrom", "Waldenstrom's macroglobulinaemia", "macroglobulinemia, Waldenström's", "waldenstrom's macroglobulinaemia", "Waldenstrom's Macroglobulinaemia", "Waldenstroem's macroglobulinemia", "Macroglobulinaemia, Waldenstrom's", "Von Waldenstrom macroglobulinemia", "Waldenstrom's macroglobulinaemias", "Von Waldenstrom macroglobulinaemia", "Waldenstrom's macroglobulinemia NOS", "Lymphoma, Lymphocytic, Plasmacytoid", "Waldenstrom's macroglobulinaemia NOS", "familial Waldenström macroglobulinemia", "Familial Waldenstrom Macroglobulinemia", "Familial Waldenström Macroglobulinemia", "Monoclonal immunoglobulin M proteinemia", "Waldenström macroglobulinemia, familial", "Familial Waldenstrom Macroglobulinaemia", "Familial Waldenstroms Macroglobulinaemia", "Waldenström macroglobulinemia (disorder)", "Familial Waldenstrom's Macroglobulinaemia", "Macroglobulinaemia, Familial Waldenstrom's", "Waldenstrom's Macroglobulinaemia, Familial", "Waldenstrom's macroglobulinemia (diagnosis)", "lymphoplasmacytic lymphoma with IgM gammopathy", "Lymphoplasmacytic Lymphoma/Waldenström Macroglobulinemia", "Waldenstrom's macroglobulinemia (morphologic abnormality)", "Lymphoplasmacytic Lymphoma/Waldenström's Macroglobulinemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Waldenstrom macroglobulinemia", "shortest_name_length": 17}
{"curie": "MONDO:0044210", "names": ["thalassemia minor", "thalassemia trait", "THALASSEMIA MINOR", "minor thalassemia", "Thalassemia minor", "THALASSEMIA TRAIT", "Thalassemia Minor", "Thalassemia trait", "minor; thalassemia", "thalassaemia minor", "Thalassaemia minor", "thalassemia; minor", "thalassemia; trait", "thalassemia traits", "thalassaemia trait", "THALLASSEMIA MINOR", "trait; thalassemia", "Thalassaemia trait", "Thalassemia trait NOS", "Thalassemia trait, NOS", "beta thalassemia trait", "Thalassemia minor, NOS", "heterozygous thalassemia", "Heterozygous thalassemia", "Heterozygous thalassaemia", "thalassemia trait (diagnosis)", "thalassemia minor (diagnosis)", "Heterozygous thalassemia, NOS", "Heterozygous thalassemia (disorder)", "ANEMIA, HEMOLYTIC, THALASSEMIA MINOR", "Thalassemia Minor (beta Thalassemia Minor)", "Thalassemia Minor (beta-Thalassemia Minor)", "Minor, Thalassemia (beta-Thalassemia Minor)", "Thalassemia Minors (beta-Thalassemia Minor)", "trait; abnormal hemoglobin with thalassemia", "Minors, Thalassemia (beta-Thalassemia Minor)", "hemoglobin; trait, abnormal hemoglobin with thalassemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thalassemia minor", "shortest_name_length": 17}
{"curie": "MONDO:0004717", "names": ["PELIOSIS HEPATIS", "Hepatic peliosis", "PURPURA, HEPATIS", "hepatic peliosis", "peliosis hepatis", "Hepatis peliosis", "HEPATIS PELIOSIS", "Peliosis Hepatis", "Peliosis hepatis", "Hepatis, Peliosis", "hepatis; peliosis", "peliosis; hepatis", "Peliosis hepatitis", "PELIOSIS HEPATITIS", "peliosis hepatitis", "LIVER, ANGIOMATOSIS", "angiomatosis; liver", "liver; angiomatosis", "PH - Peliosis hepatis", "Telangiectasis of liver", "Peliosis hepatis (disorder)", "peliosis hepatis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peliosis hepatis", "shortest_name_length": 16}
{"curie": "UMLS:C0854985", "names": ["Stage I Lung Adenocarcinoma", "Lung adenocarcinoma stage I", "Adenocarcinoma lung stage I", "Lung Adenocarcinoma, Stage I", "Adenocarcinoma of lung stage I", "Stage I Adenocarcinoma of Lung", "Adenocarcinoma of lung, stage I", "Stage I Adenocarcinoma of the Lung", "Stage I Lung Adenocarcinoma AJCC v7", "Finding of adenocarcinoma of lung, stage I", "Adenocarcinoma of lung, stage I (disorder)", "clinical finding tumor stage adenocarcinoma of lung, stage I", "Finding of adenocarcinoma of lung, stage I (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma of lung, stage I", "shortest_name_length": 27}
{"curie": "MONDO:0001031", "names": ["Acute purulent otitis media", "acute purulent otitis media", "purulent acute otitis media", "Acute otitis media, purulent", "Otitis media suppurative acute", "otitis; media, purulent, acute", "otitis; media, acute, purulent", "Acute suppurative otitis media", "Otitis media;suppurative;acute", "acute suppurative otitis media", "suppurative otitis media, acute", "suppurative; otitis media, acute", "OTITIS MEDIA, SUPPURATIVE, ACUTE", "otitis; media, suppurative, acute", "otitis; media, acute, suppurative", "Otitis media suppurative acute NOS", "Acute suppurative otitis media, NOS", "ASOM - Acute suppurative otitis media", "Acute suppurative otitis media (disorder)", "acute suppurative otitis media (diagnosis)", "Acute suppurative otitis media in diseases classified elsewhere"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "purulent acute otitis media", "shortest_name_length": 27}
{"curie": "MONDO:0020702", "names": ["autosomal dominant epidermolytic ichthyosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant epidermolytic ichthyosis", "shortest_name_length": 43}
{"curie": "UMLS:C1527348", "names": ["Brain hypoxia", "brain hypoxia", "Brain Hypoxia", "Hypoxia, Brain", "cerebral hypoxia", "Cerebral Hypoxia", "Cerebral hypoxia", "hypoxia cerebral", "Hypoxia of brain", "cerebral; hypoxia", "Hypoxia, Cerebral", "hypoxia; cerebral", "Hypoxia of brain (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brain Hypoxia", "shortest_name_length": 13}
{"curie": "MONDO:0005881", "names": ["Scanty liquor", "Oligohydramnios", "OLIGOHYDRAMNIOS", "oligohydramnios", "Deficient liquor", "Oligohydramnios, NOS", "Reduced liquor volume", "Reduced Amniotic Fluid", "Amniotic fluid index low", "Maternal oligohydramnios", "delivered oligohydramnios", "oligohydramnios (disease)", "antepartum oligohydramnios", "Oligohydramnios (disorder)", "oligohydramnios (diagnosis)", "Oligohydramnios - delivered", "oligohydramnios - delivered", "Low levels of amniotic fluid", "Amniotic fluid index decreased", "AMNIOTIC FLUID INDEX DECREASED", "Decreased amniotic fluid index", "Oligohydramnios, unspecified trimester"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oligohydramnios", "shortest_name_length": 13}
{"curie": "MONDO:0800110", "names": ["PTI, aberrant", "persistent tachypnoe of infancy, aberrant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "persistent tachypnoe of infancy, aberrant", "shortest_name_length": 13}
{"curie": "MONDO:0020718", "names": ["CSBS", "Pseudoobstructive Syndrome", "Syndrome, Pseudoobstructive", "Pseudoobstructive Syndromes", "intestine pseudoobstruction", "INTESTINE, PSEUDOOBSTRUCTION", "Intestinal Pseudoobstruction", "intestinal pseudoobstruction", "INTESTINE PSEUDO OBSTRUCTION", "Intestinal pseudoobstruction", "intestinal pseudo-obstruction", "intestinal pseudo obstruction", "pseudo obstruction intestinal", "Intestinal Pseudo-Obstruction", "Intestinal Pseudo Obstruction", "Pseudoobstruction, Intestinal", "Intestinal pseudo-obstruction", "pseudo intestinal obstruction", "Intestinal Pseudoobstructions", "Intestinal Pseudo-Obstructions", "Pseudo Obstruction, Intestinal", "Pseudo-Obstruction, Intestinal", "Pseudo-obstruction of intestine", "congenital short bowel syndrome", "congenital short bowel syndrome 1", "Pseudointestinal Obstruction Syndrome", "Obstruction Syndrome, Pseudointestinal", "Pseudointestinal Obstruction Syndromes", "Syndrome, Pseudointestinal Obstruction", "Idiopathic Intestinal Pseudo-Obstruction", "Intestinal Pseudo-Obstruction, Idiopathic", "Intestinal Pseudo Obstruction, Idiopathic", "intestinal pseudo-obstruction (diagnosis)", "Idiopathic Intestinal Pseudo-Obstructions", "Intestinal Pseudo-Obstructions, Idiopathic", "Pseudo-obstruction of intestine (disorder)", "Chronic Idiopathic Intestinal Pseudo Obstruction", "Chronic Idiopathic Intestinal Pseudo-Obstruction", "congenital short bowel syndrome, autosomal recessive", "congenital short bowel syndrome due to CLMP variation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital short bowel syndrome, autosomal recessive", "shortest_name_length": 4}
{"curie": "MONDO:0020721", "names": ["XLSA", "ANH1", "SIDBA1", "ANEMIA, HYPOCHROMIC", "anemia, hypochromic", "sideroblastic anemia 1", "sideroblastic anaemia 1", "anemia, sideroblastic, 1", "ANEMIA, SIDEROBLASTIC, 1", "X-linked sideroblastic anemia", "sideroblastic anemia X-linked", "X-linked sideroblastic anaemia", "sideroblastic anemia, X-linked", "HEREDITARY IRON-LOADING ANEMIA", "hereditary iron-loading Anemia", "Hereditary Iron-Loading Anemia", "ANEMIA, SIDEROBLASTIC, X-LINKED", "anemia, sideroblastic, X-linked", "Hereditary Sideroblastic Anemia", "anemia hereditary sideroblastic", "congenital sideroblastic anemia", "Hereditary sideroblastic anemia", "Anemia, Sideroblastic, X-Linked", "Congenital sideroblastic anemia", "X-linked sideroblastic anemia 1", "Congenital Sideroblastic Anaemia", "Sideroblastic anemia, hereditary", "Congenital sideroblastic anaemia", "Anemia, congenital sideroblastic", "Anemia, hereditary sideroblastic", "ANEMIA, HEREDITARY SIDEROBLASTIC", "Hereditary sideroblastic anaemia", "anemia, hereditary sideroblastic", "Anemia, Hereditary Sideroblastic", "anemia; sideroblastic, hereditary", "Constitutional sideroblastic anemia", "Hereditary sideroblastic anemia, NOS", "Hereditary sideroblastic anaemia, NOS", "X chromosome-linked sideroblastic anemia", "X Chromosome-Linked Sideroblastic Anemia", "X chromosome-linked sideroblastic anaemia", "sex-linked hypochromic sideroblastic anemia", "anemia sex-linked hypochromic sideroblastic", "Sex-linked hypochromic sideroblastic anemia", "congenital sideroblastic anemia (diagnosis)", "Anemia, Sex-Linked Hypochromic Sideroblastic", "Anemia, sex-linked hypochromic sideroblastic", "anemia, sideroblastic, 1, X-linked recessive", "X chromosome-linked sideroblastic anemia, NOS", "anemia; sideroblastic, hypochromic, sex-linked", "X chromosome-linked sideroblastic anaemia, NOS", "anemia; hypochromic, sideroblastic, sex-linked", "Erythroid 5-Aminolevulinate Synthase Deficiency", "erythroid 5-aminolevulinate synthase deficiency", "Erythroid 5-aminolevulinate synthetase deficiency", "X chromosome-linked sideroblastic anemia (disorder)", "X-Linked Pyridoxine-Responsive Sideroblastic Anemia", "sex-linked hypochromic sideroblastic anemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked sideroblastic anemia 1", "shortest_name_length": 4}
{"curie": "MONDO:0023154", "names": ["Jaffe-Campanacci syndrome", "jaffe-campanacci syndrome", "Jaffe Campanacci syndrome", "jaffe campanacci syndrome", "fibromatosis multiple non ossifying", "Multiple non-ossifying fibromatosis", "disseminated nonossifying fibromas in association with cafe-au-lait spots"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibromatosis multiple non ossifying", "shortest_name_length": 25}
{"curie": "MONDO:0003342", "names": ["Benign Pericytic Tumor", "benign Pericytic tumor", "benign perivascular tumor", "benign Pericytic neoplasm", "Benign Perivascular Tumor", "Benign Pericytic Neoplasm", "benign pericytic neoplasm", "pericytic neoplasm, benign", "benign perivascular neoplasm", "Benign Perivascular Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign perivascular tumor", "shortest_name_length": 22}
{"curie": "MONDO:0043786", "names": ["Serositis", "serositis", "Serositides", "serositides", "Serositis (disorder)", "Serositis (diagnosis)", "serous membrane inflammation", "inflammation of serous membrane", "inflammatory soft tissue disorders serositis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "serositis", "shortest_name_length": 9}
{"curie": "MONDO:0001455", "names": ["Lattice degeneration", "Lattice degenerations", "LD - Lattice degeneration", "degeneration lattice retina", "lattice degeneration retina", "Retinal lattice degeneration", "Lattice retinal degeneration", "retinal lattice degeneration", "Lattice degeneration of retina", "Palisade degeneration of retina", "palisade degeneration of retina", "Lattice degeneration of the retina", "lattice peripheral retinal degeneration", "Retinal lattice degeneration (disorder)", "retinal lattice degeneration (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal lattice degeneration", "shortest_name_length": 20}
{"curie": "MONDO:0011550", "names": ["fibromatosis, gingival, with hypertrichosis and mental retardation", "Fibromatosis, Gingival, with Hypertrichosis and Mental Retardation", "FIBROMATOSIS, GINGIVAL, WITH HYPERTRICHOSIS AND MENTAL RETARDATION", "fibromatosis, gingival, with hypertrichosis and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibromatosis, gingival, with hypertrichosis and intellectual disability", "shortest_name_length": 66}
{"curie": "MONDO:0003609", "names": ["seminal vesicle cystadenoma", "Seminal Vesicle Cystadenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "seminal vesicle cystadenoma", "shortest_name_length": 27}
{"curie": "MONDO:0021747", "names": ["Acanthamoebosis", "acanthamebiasis", "Acanthamebiases", "acanthamoebosis", "Acanthamebiasis", "Acanthamoebiasis", "acanthamoebiasis", "Acanthameba infection", "infection; Acanthameba", "Acanthameba; infection", "Acanthamoeba Infection", "Acanthamoeba infection", "Acanthamoeba; infection", "Acanthamoeba Infections", "infection; Acanthamoeba", "Infection, Acanthamoeba", "infections, Acanthamoeba", "Acanthameba infection NOS", "Infection by Acanthamoeba", "infection by Acanthamoeba", "Acanthamoeba infection NOS", "Acanthamebiasis, unspecified", "Infection by Acanthamoeba, NOS", "Acanthamoeba infectious disease", "Infection caused by Acanthamoeba", "infection caused by Acanthamoeba", "Infection caused by Acanthamoeba (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acanthamoeba infectious disease", "shortest_name_length": 15}
{"curie": "MONDO:0030979", "names": ["MLEHFB", "ENDOVESLB", "endove syndrome, limb-brain type", "ENDOVE SYNDROME, LIMB-BRAIN TYPE", "Mesomelia of Lower Extremities With Hand, Foot, and Brain Anomalies", "MESOMELIA OF LOWER EXTREMITIES WITH HAND, FOOT, AND BRAIN ANOMALIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endove syndrome, limb-brain type", "shortest_name_length": 6}
{"curie": "UMLS:C4288414", "names": ["Pelvic Fibromatosis", "Pelvic Desmoid Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pelvic Fibromatosis", "shortest_name_length": 19}
{"curie": "UMLS:C5554909", "names": ["Metastatic Microsatellite Stable Colon Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Microsatellite Stable Colon Carcinoma", "shortest_name_length": 48}
{"curie": "MONDO:0017326", "names": ["IDH", "IDH Gene Family", "IDH Gene family", "Isocitrate Dehydrogenase Gene Family", "isocitrate dehydrogenase Gene family", "infective dermatitis associated with HTLV-1", "infective dermatitis associated with human T-lymphotropic virus type 1", "infective dermatitis associated with human T-lymphotropic virus type I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infective dermatitis associated with HTLV-1", "shortest_name_length": 3}
{"curie": "UMLS:C5555127", "names": ["Recurrent Aggressive T-Cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Aggressive T-Cell Non-Hodgkin Lymphoma", "shortest_name_length": 48}
{"curie": "MONDO:0011481", "names": ["CSB", "CRS2", "craniosynostosis 2", "CRANIOSYNOSTOSIS 2", "craniosynostosis type 2", "Craniosynostosis, Type 2", "CRANIOSYNOSTOSIS, TYPE 2", "craniosynostosis Warman type", "Craniosynostosis Boston type", "Craniosynostosis Warman type", "MSX2-related craniosynostosis", "Craniosynostosis, Boston type", "CRANIOSYNOSTOSIS, BOSTON-TYPE", "Craniosynostosis, Boston-Type", "Craniosynostosis, Warman type", "craniosynostosis, Warman type", "Warman-Mulliken-Hayward syndrome", "Warman Mulliken Hayward syndrome", "Craniosynostosis Boston type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniosynostosis 2", "shortest_name_length": 3}
{"curie": "MONDO:0007635", "names": ["Frasier syndrome", "FRASIER SYNDROME", "frasier syndrome", "Frasier Syndrome", "frasiers syndrome", "Syndrome, Frasier", "Frasier syndrome (disorder)", "Frasier syndrome, autosomal dominant, somatic mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Frasier syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0060752", "names": ["NEDSG", "neurodevelopmental disorder with spasticity and poor growth", "NEURODEVELOPMENTAL DISORDER WITH SPASTICITY AND POOR GROWTH"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with spasticity and poor growth", "shortest_name_length": 5}
{"curie": "UMLS:C2828193", "names": ["Stage IVB Gestational Trophoblastic Tumor", "Stage IVB Gestational Trophoblastic Tumor AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Gestational Trophoblastic Tumor AJCC v7", "shortest_name_length": 41}
{"curie": "UMLS:C2987120", "names": ["Intramucosal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intramucosal Adenocarcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0100347", "names": ["Hormonal tumor", "Hormonal tumour", "syndrome serotonin", "Carcinoid Syndrome", "serotonin syndrome", "Serotonin syndrome", "Carcinoid syndrome", "CARCINOID SYNDROME", "carcinoid syndrome", "carcinoids syndrome", "syndrome; carcinoid", "carcinoid; syndrome", "carcinoid tumor syndrome", "carcinoid tumors, intestinal", "Malignant carcinoid syndrome", "Malignant Carcinoid Syndrome", "malignant carcinoid syndrome", "Syndrome, Malignant Carcinoid", "Excessive serotonin secretion", "Malignant Carcinoid Syndromes", "Carcinoid Syndrome, Malignant", "Carcinoid syndrome (disorder)", "Carcinoid Syndromes, Malignant", "Syndromes, Malignant Carcinoid", "carcinoid syndrome (diagnosis)", "hormone secretion; carcinoid tumor", "carcinoid; hormone secretion, tumor", "secretion; carcinoid tumor, hormone", "Hormone secretion by carcinoid tumor", "Hormone secretion by carcinoid tumors", "Hormone secretion by carcinoid tumour"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoid syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0033850", "names": ["autosomal recessive axonal charcot-marie-tooth disease due to copper metabolism defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive axonal charcot-marie-tooth disease due to copper metabolism defect", "shortest_name_length": 86}
{"curie": "MONDO:0032777", "names": ["GEFSP10", "GEFS+10", "GEFS+, TYPE 10", "Gefs+, Type 10", "generalized epilepsy with febrile seizures plus 10", "generalised epilepsy with febrile seizures plus 10", "generalised epilepsy with febrile seizures plus type 10", "generalized epilepsy with febrile seizures plus type 10", "GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 10", "generalized epilepsy with febrile seizures plus, type 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "generalized epilepsy with febrile seizures plus, type 10", "shortest_name_length": 7}
{"curie": "MONDO:0002245", "names": ["thrombocytopathy", "Platelet Disorder", "platelet disorder", "Platelet Abnormality", "platelet abnormality", "blood platelet disease", "Blood Platelet Disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blood platelet disease", "shortest_name_length": 16}
{"curie": "UMLS:C0158350", "names": ["tendon contracture", "Tendon contracture", "contracture tendon", "contracture tendons", "tendon; contracture", "contracture; tendon", "Contracture of tendon", "tendinous contracture", "contracture of tendon", "CONTRACTURE TENDINOUS", "Tendinous contracture", "TENDINOUS CONTRACTURE", "Contracture tendinous", "contracture of tendon sheath", "Contracture of tendon sheath", "Tendon contracture (disorder)", "Contracture of tendon (sheath)", "Contracture of tendon sheath (disorder)", "contracture of tendon sheath (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Contracture of tendon sheath", "shortest_name_length": 18}
{"curie": "MONDO:0009416", "names": ["HIHGHH", "HYPOINSULINEMIC HYPOGLYCEMIA AND HEMIHYPERTROPHY", "HYPOINSULINEMIC HYPOGLYCEMIA WITH HEMIHYPERTROPHY", "hypoinsulinemic hypoglycemia with hemihypertrophy", "hypoinsulinemic hypoglycemia and body hemihypertrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypoinsulinemic hypoglycemia and body hemihypertrophy", "shortest_name_length": 6}
{"curie": "MONDO:0016970", "names": ["partial trisomy of chromosome 20q", "partial duplication of chromosome 20q", "partial trisomy of the long arm of chromosome 20", "partial duplication of the long arm of chromosome 20", "partial trisomy of the long arm of chromosome type 20"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial trisomy of the long arm of chromosome 20", "shortest_name_length": 33}
{"curie": "MONDO:0017004", "names": ["partial deletion of chromosome Xp", "partial monosomy of chromosome Xp", "partial monosomy of the short arm of chromosome X", "partial deletion of the short arm of chromosome X", "partial monosomy of the short arm of chromosome type X"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial monosomy of the short arm of chromosome X", "shortest_name_length": 33}
{"curie": "UMLS:C0432562", "names": ["spleen lymphoma", "lymphoma spleen", "Splenic Lymphoma", "splenic lymphoma", "lymphoma splenic", "Splenic lymphoma", "Primary Splenic Lymphoma", "Malignant lymphoma of spleen", "malignant lymphoma of spleen", "Malignant lymphoma, NOS of spleen", "Malignant lymphoma of spleen (disorder)", "malignant lymphoma of spleen (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant lymphoma of spleen", "shortest_name_length": 15}
{"curie": "MONDO:0004069", "names": ["Mitochondrial Disease", "mitochondrial disease", "disease mitochondrial", "Mitochondrial disease", "Mitochondrial Disorder", "mitochondrial disorder", "Disease, Mitochondrial", "Mitochondrial Diseases", "mitochondrial diseases", "disorders mitochondrial", "MITOCHONDRIAL CYTOPATHY", "Mitochondrial cytopathy", "Mitochondrial Disorders", "Disorder, Mitochondrial", "mitochondrial disorders", "Disorders, Mitochondrial", "mitochondrial disease/disorder", "mitochondrial genetic disorders", "mitochondrial metabolism disease", "Mitochondrial cytopathy (disorder)", "inborn mitochondrial metabolism disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn mitochondrial metabolism disorder", "shortest_name_length": 21}
{"curie": "UMLS:C3267180", "names": ["Infant Formula Intolerance", "Infant formula intolerance", "Intolerance to infant formula", "Breast milk substitute intolerance", "Breast Milk Substitute Intolerance", "Intolerance to infant formula (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intolerance to infant formula", "shortest_name_length": 26}
{"curie": "UMLS:C1699648", "names": ["Ileal obstruction", "Ileal Obstruction", "Ileal obstruction (diagnosis)", "obstruction of small intestine ileum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ileal Obstruction", "shortest_name_length": 17}
{"curie": "MONDO:0006746", "names": ["Becker's disease", "becker's disease", "FIBROSIS ENDOCARDIAL", "endocardial fibrosis", "Fibrosis endocardial", "Endocardial fibrosis", "endocardium; fibrosis", "fibrosis; endocardium", "endomyocardial fibrosis", "Endomyocardial Fibroses", "Endomyocardial fibrosis", "Endomyocardial Fibrosis", "Fibroses, Endomyocardial", "endomyocardial; fibrosis", "Endomyocardial sclerosis", "endomyocardial sclerosis", "Fibrosis, Endomyocardial", "fibrosis; endomyocardial", "FIBROSIS, ENDOMYOCARDIAL", "Sclerosis, endomyocardial", "obscure African cardiomyopathy", "Obscure African cardiomyopathy", "African endomyocardial fibrosis", "Obscure cardiomyopathy of Africa", "obscure cardiomyopathy of africa", "cardiomyopathy; obscure of Africa", "obscure of Africa; cardiomyopathy", "Endomyocardial fibrosis (disorder)", "endomyocardial fibrosis (diagnosis)", "Idiopathic mural endomyocardial disease", "Restrictive cardiomyopathy with endomyocardial fibrosis", "Restrictive cardiomyopathy with endomyocardial fibrosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endomyocardial fibrosis", "shortest_name_length": 16}
{"curie": "MONDO:0002969", "names": ["ciliary body cancer", "cancer of ciliary body", "neoplasm of ciliary body", "tumor of the Ciliary body", "tumor of the ciliary body", "malignant ciliary body tumor", "Malignant Ciliary Body Tumor", "Malignant Tumor of Ciliary Body", "malignant tumor of ciliary body", "Malignant tumor of ciliary body", "malignant ciliary body neoplasm", "Malignant Ciliary Body Neoplasm", "Malignant tumour of ciliary body", "malignant neoplasm of ciliary body", "Malignant Neoplasm of Ciliary Body", "Malignant neoplasm of ciliary body", "malignant tumor of the ciliary body", "Malignant Tumor of the Ciliary Body", "malignant tumor of the Ciliary body", "malignant neoplasm of the ciliary body", "Malignant Neoplasm of the Ciliary Body", "Malignant tumor of ciliary body (disorder)", "malignant neoplasm of ciliary body (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ciliary body cancer", "shortest_name_length": 19}
{"curie": "MONDO:0006837", "names": ["Low tension glaucoma", "low tension glaucoma", "Low-tension glaucoma", "Low Tension Glaucoma", "GLAUCOMA LOW TENSION", "tension glaucoma, Low", "glaucoma; low-tension", "Low Tension Glaucomas", "Glaucoma, low tension", "glaucoma, Low tension", "low-tension; glaucoma", "Glaucoma, Low Tension", "low tension Glaucomas", "tension Glaucomas, Low", "Glaucomas, Low tension", "Normal tension glaucoma", "glaucoma normal tension", "Normal Tension Glaucoma", "normal tension glaucoma", "Normal Tension Glaucomas", "pressure normal glaucoma", "glaucoma, normal tension", "tension glaucoma, normal", "normal pressure glaucoma", "Normal pressure glaucoma", "normal tension Glaucomas", "Glaucoma, Normal Tension", "Glaucomas, normal tension", "tension Glaucomas, normal", "LTG - Low tension glaucoma", "Low tension glaucoma (disorder)", "low tension open-angle glaucoma", "Low tension open-angle glaucoma", "low tension open-angle glaucoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "low tension glaucoma", "shortest_name_length": 20}
{"curie": "UMLS:C1167662", "names": ["Diabetic fetopathy", "Diabetic Fetopathy", "Diabetic foetopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diabetic foetopathy", "shortest_name_length": 18}
{"curie": "UMLS:C0242514", "names": ["Reciprocal Tachycardia", "Tachycardia, Reciprocal", "Reciprocal Tachycardias", "Tachycardias, Reciprocal", "Reciprocating tachycardia", "Reciprocating Tachycardia", "Tachycardia, Reciprocating", "Reciprocating Tachycardias", "Tachycardias, Reciprocating"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tachycardia, Reciprocating", "shortest_name_length": 22}
{"curie": "UMLS:C2981638", "names": ["Stage IVB Hilar Cholangiocarcinoma", "Stage IVB Hilar Cholangiocarcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Hilar Cholangiocarcinoma AJCC v7", "shortest_name_length": 34}
{"curie": "MONDO:0016972", "names": ["partial trisomy of chromosome 22q", "partial duplication of chromosome 22q", "partial trisomy of the long arm of chromosome 22", "partial duplication of the long arm of chromosome 22", "partial duplication of the long arm of chromosome type 22"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of the long arm of chromosome 22", "shortest_name_length": 33}
{"curie": "UMLS:C5555675", "names": ["Unresectable Digestive System Carcinoid Tumor", "Unresectable Digestive System Neuroendocrine Tumor G1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Digestive System Neuroendocrine Tumor G1", "shortest_name_length": 45}
{"curie": "UMLS:C4683147", "names": ["Stage I Posterior Uveal Melanoma AJCC v8", "Stage I Choroidal and Ciliary Body Melanoma", "Stage I Choroidal and Ciliary Body Melanoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Choroidal and Ciliary Body Melanoma AJCC v8", "shortest_name_length": 40}
{"curie": "MONDO:0015391", "names": ["nasopharynx teratoma", "nasopharyngeal teratoma", "Nasopharyngeal teratoma", "Teratoma of the nasopharynx", "teratoma of the nasopharynx"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasopharyngeal teratoma", "shortest_name_length": 20}
{"curie": "UMLS:C0011164", "names": ["degenerate", "Degenerated", "degenerates", "degenerated", "Degenerative", "degenerating", "DEGENERATION", "degenerative", "Degeneration", "DEGENERATIVE", "degeneration", "DEGENERATIONS", "degenerations", "Degenerations", "Degeneration, NOS", "Tissue Degeneration", "degenerative change", "Degenerative change", "Degenerative changes", "abnormal degeneration", "Abnormal degeneration", "Degenerative abnormality", "DEGENERATIVE ABNORMALITIES", "Degenerative abnormality (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abnormal degeneration", "shortest_name_length": 10}
{"curie": "UMLS:C3897493", "names": ["Stent Thrombosis", "Stent thrombosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stent thrombosis", "shortest_name_length": 16}
{"curie": "MONDO:0007919", "names": ["PCL", "LMPH1", "LMPH1A", "Milroy", "LMPHM1", "Nonne-Milroy", "edema; Milroy", "Milroy; edema", "Milroy disease", "Milroy Disease", "milroy disease", "MILROY DISEASE", "milroys disease", "Milroys Disease", "LMPH1A, FORMERLY", "milroy's disease", "Milroy's Disease", "Milroy's disease", "Nonne’s syndrome", "Milroy lymphedema", "Milroy lymphoedema", "Primary lymphedema", "primary lymphedema", "lymphedema primary", "Primary Lymphedema", "Primary lymphoedema", "primary lymphoedema", "Nonne Milroy Disease", "Nonne-Milroy disease", "Nonne-Milroy Disease", "Nonne-Milroy syndrome", "Lymphedema congenital", "congenital lymphedema", "Congenital lymphedema", "lymphedema congenital", "Hereditary Lymphedema", "Hereditary lymphedema", "hereditary lymphedema", "Congenital lymphoedema", "Early-Onset Lymphedema", "lymphedema; hereditary", "early onset lymphedema", "Hereditary Lymphedemas", "Lymphedema, Hereditary", "Lymphoedema congenital", "Hereditary lymphoedema", "Early Onset Lymphedema", "LYMPHEDEMA, HEREDITARY", "hereditary lymphoedema", "hereditary; lymphedema", "hereditary lymphedema I", "Nonne-Milroy lymphedema", "Hereditary Lymphedema 1", "Early Onset Lymphedemas", "Lymphedema, Early Onset", "Lymphedema, Early-Onset", "Nonne-Milroy Lymphedema", "lymphedema, early-onset", "Early-Onset Lymphedemas", "hereditary lymphedema 1", "Lymphedemas, Hereditary", "LYMPHEDEMA, EARLY-ONSET", "NONNE-MILROY LYMPHEDEMA", "Nonne Milroy Lymphedema", "Hereditary Lymphedema 1s", "Lymphedemas, Early-Onset", "Lymphedema, Nonne-Milroy", "LYMPHATIC MALFORMATION 1", "Lymphedemas, Early Onset", "lymphatic malformation 1", "hereditary lymphedema IA", "Nonne-Milroy lymphoedema", "Lymphedema, Hereditary, Ia", "FLT4 hereditary lymphedema", "Nonne Milroy Meige Disease", "lymphedema, hereditary, 1A", "Nonne-Milroy-Meige Disease", "NONNE-MILROY-MEIGE SYNDROME", "hereditary lymphedema type I", "Hereditary Lymphedema Type I", "Hereditary lymphedema type I", "Milroy's disease (diagnosis)", "PRIMARY CONGENITAL LYMPHEDEMA", "primary congenital lymphedema", "congenital primary lymphedema", "Primary Congenital Lymphedema", "Hereditary lymphoedema type I", "Primary congenital lymphedema", "Congenital Familial Lymphedema", "Primary Congenital Lymphedemas", "Congenital Lymphedema, Primary", "Primary congenital lymphoedema", "Lymphedema, Primary Congenital", "Infantile lymphedema (praecox)", "Infantile lymphoedema (praecox)", "Congenital Lymphedemas, Primary", "Primary (congenital) lymphedema", "lymphedema, hereditary, type 1A", "Lymphedemas, Primary Congenital", "Hereditary lymphedema (disorder)", "Primary (congenital) lymphoedema", "congenital hereditary lymphedema", "Congenital Hereditary Lymphedema", "congenital lymphedema (diagnosis)", "Congenital Hereditary Lymphedemas", "Lymphedema, Congenital Hereditary", "Hereditary lymphedema (diagnosis)", "Hereditary Lymphedema, Congenital", "Lymphedemas, Congenital Hereditary", "Hereditary Lymphedemas, Congenital", "LYMPHEDEMA, HEREDITARY, IA, FORMERLY", "anomalies of skin hereditary lymphedema", "Hereditary lymphedema type I (disorder)", "LYMPHEDEMA, HEREDITARY, TYPE I, FORMERLY", "hereditary lymphedema caused by mutation in FLT4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphatic malformation 1", "shortest_name_length": 3}
{"curie": "UMLS:C1955906", "names": ["Extranodal NK T Cell Lymphoma", "Extranodal NK/T-cell lymphoma", "Extranodal NK-T-Cell Lymphoma", "NK-T-Cell Lymphoma, Extranodal", "Extranodal NK-T-Cell Lymphomas", "Lymphoma, Extranodal NK T Cell", "Lymphoma, Extranodal NK-T-Cell", "Lymphomas, Extranodal NK-T-Cell", "NK-T-Cell Lymphomas, Extranodal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoma, Extranodal NK-T-Cell", "shortest_name_length": 29}
{"curie": "UMLS:C3494186", "names": ["Autosomal Hemophilia A", "Hemophilia A, Autosomal", "Autosomal Hemophilia As", "As, Autosomal Hemophilia", "Hemophilia As, Autosomal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Autosomal Hemophilia A", "shortest_name_length": 22}
{"curie": "MONDO:0000222", "names": ["Gonorrhea of seminal vesicle", "Gonococcal seminal vesiculitis", "seminal vesicle acute gonorrhea", "Acute gonorrhea of seminal vesicle", "seminal vesiculitis gonococcal acute", "acute gonococcal seminal vesiculitis", "Acute gonococcal seminal vesiculitis", "gonococcal seminal vesiculitis, acute", "Gonococcal seminal vesiculitis (acute)", "Acute gonococcal seminal vesiculitis (disorder)", "Acute gonococcal seminal vesiculitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "seminal vesicle acute gonorrhea", "shortest_name_length": 28}
{"curie": "UMLS:C1449647", "names": ["Secondary Peritonitis", "secondary peritonitis", "Peritonitis, Secondary", "secondary peritonitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary Peritonitis", "shortest_name_length": 21}
{"curie": "MONDO:0054601", "names": ["PITA5", "pituitary adenoma 5", "pituitary adenoma 5, multiple types", "PITUITARY ADENOMA 5, MULTIPLE TYPES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pituitary adenoma 5, multiple types", "shortest_name_length": 5}
{"curie": "UMLS:C4744389", "names": ["Sellar Embryonal Carcinoma", "Embryonal Carcinoma of the Sellar Region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sellar Embryonal Carcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0006490", "names": ["vagina epidermoid carcinoma", "VAGINAL CANCER SQUAMOUS CELL", "vaginal squamous cell cancer", "vaginal epidermoid carcinoma", "VAGINA, CARCINOMA, EPIDERMOID", "epidermoid carcinoma of vagina", "vagina squamous cell carcinoma", "Squamous cell cancer of vagina", "vaginal squamous cell carcinoma", "Vaginal Squamous Cell Carcinoma", "vagina epidermoid cell carcinoma", "vaginal epidermoid cell carcinoma", "carcinoma, squamous cell, vaginal", "carcinoma of vagina squamous cell", "Vaginal Squamous Cell Cancer, NOS", "squamous cell carcinoma of vagina", "Squamous cell carcinoma of vagina", "vaginal squamous cell cancer, NOS", "epidermoid carcinoma of the vagina", "epidermoid cell carcinoma of vagina", "carcinoma, epidermoid cell, vaginal", "VAGINAL CANCER, EPIDERMOID CARCINOMA", "Vaginal Squamous Cell Carcinoma, NOS", "squamous cell carcinoma of the vagina", "Squamous cell carcinoma of the vagina", "vagina cancer, squamous cell carcinoma", "epidermoid cell carcinoma of the vagina", "vaginal cancer, squamous cell carcinoma", "vagina cancer, epidermoid cell carcinoma", "vaginal cancer, epidermoid cell carcinoma", "squamous cell carcinoma of the vulva/vagina", "Squamous cell carcinoma of vagina (disorder)", "squamous cell carcinoma of vagina (diagnosis)", "Vaginal Squamous Cell Carcinoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vaginal squamous cell carcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C0854337", "names": ["Genitourinary tract gonococcal infection", "Gonococcal Infection of Genitourinary Tract", "Genitourinary tract gonococcal infection NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Genitourinary tract gonococcal infection", "shortest_name_length": 40}
{"curie": "MONDO:0004685", "names": ["Waldeyer ring cancer", "tonsillar ring cancer", "Waldeyer's ring cancer", "cancer of tonsillar ring", "Malignant tumor of Waldeyer ring", "Malignant tumour of Waldeyer ring", "malignant tonsillar ring neoplasm", "Malignant tumor of Waldeyer's ring", "malignant tumor of Waldeyer's ring", "Malignant tumour of Waldeyer's ring", "malignant neoplasm of tonsillar ring", "Malignant neoplasm of Waldeyer's ring", "Malignant neoplasm of waldeyer's ring", "malignant neoplasm of Waldeyer's ring", "Malignant tumor of Waldeyer's ring (disorder)", "malignant neoplasm of Waldeyer's ring (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Waldeyer's ring cancer", "shortest_name_length": 20}
{"curie": "UMLS:C1335733", "names": ["Regressing Skin Melanoma", "Regressing Melanoma of Skin", "regressing melanoma of skin", "Regressing Cutaneous Melanoma", "Regressing Melanoma of the Skin", "Regressing Malignant Skin Melanoma", "Regressing Cutaneous (Skin) Melanoma", "Regressing Malignant Melanoma of Skin", "regressing melanoma of skin (diagnosis)", "Regressing Malignant Melanoma of the Skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "regressing melanoma of skin", "shortest_name_length": 24}
{"curie": "UMLS:C0346957", "names": ["cancer metastatic", "metastatic cancer", "Generalised cancer", "Generalized cancer", "cancers metastatic", "Disseminated cancer", "generalize malignancy", "Generalised malignancy", "Generalized malignancy", "Disseminated malignancy", "CA - Disseminated cancer", "Malignant neoplasm disseminated", "Disseminated malignant neoplasm", "Disseminated Malignant Neoplasm", "malignant neoplasm disseminated", "Malignant neoplasm, disseminated", "Widespread metastatic malignant neoplastic disease", "metastatic cancer widespread malignant neoplastic disease", "Widespread metastatic malignant neoplastic disease (disorder)", "Disseminated malignant neoplasm without specification of site", "Widespread metastatic malignant neoplastic disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disseminated Malignant Neoplasm", "shortest_name_length": 17}
{"curie": "MONDO:0012753", "names": ["ALS9", "ALS9 (diagnosis)", "AMYOTROPHIC LATERAL SCLEROSIS 9", "amyotrophic lateral sclerosis 9", "Amyotrophic Lateral Sclerosis 9", "ANG amyotrophic lateral sclerosis", "amyotrophic lateral sclerosis ALS9", "amyotrophic lateral sclerosis type 9", "amyotrophic lateral sclerosis caused by mutation in ANG"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyotrophic lateral sclerosis type 9", "shortest_name_length": 4}
{"curie": "MONDO:0015976", "names": ["HIGM without susceptibility to opportunistic infections", "hyper-IgM syndrome without susceptibility to opportunistic infections"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyper-IgM syndrome without susceptibility to opportunistic infections", "shortest_name_length": 55}
{"curie": "UMLS:C1321135", "names": ["Paraneoplastic hyponatremia", "Paraneoplastic hyponatraemia", "Paraneoplastic hyponatremia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paraneoplastic hyponatremia", "shortest_name_length": 27}
{"curie": "MONDO:0012865", "names": ["PFB", "razor bumps", "Razor bumps", "INGROWN HAIRS", "ingrown hairs", "pili Incarnati", "PILI INCARNATI", "Pseudofolliculitis barbae", "pseudofolliculitis barbae", "PSEUDOFOLLICULITIS BARBAE", "Pseudofolliculitis barbae (disorder)", "pseudofolliculitis barbae (diagnosis)", "pseudofolliculitis barbae, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pseudofolliculitis barbae", "shortest_name_length": 3}
{"curie": "UMLS:C0948301", "names": ["Application site skin breakdown"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Application site skin breakdown", "shortest_name_length": 31}
{"curie": "UMLS:C1855496", "names": ["Contiguous gene syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Contiguous gene syndrome", "shortest_name_length": 24}
{"curie": "MONDO:0016967", "names": ["trisomy 17q", "17q trisomy", "17q duplication", "Duplication 17q", "partial trisomy 17q", "chromosome 17q duplication", "partial trisomy of chromosome 17q", "partial duplication of chromosome 17q", "partial trisomy of the long arm of chromosome 17", "partial duplication of the long arm of chromosome 17", "partial duplication of the long arm of chromosome type 17"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of the long arm of chromosome 17", "shortest_name_length": 11}
{"curie": "MONDO:0025030", "names": ["bovine foot wart", "foot wart, bovine", "bovine foot Warts", "wart, bovine foot", "foot Warts, bovine", "Warts, bovine foot", "Digital Dermatitis", "Dermatitis, Digital", "dermatitis, digital", "Digital Dermatitides", "digital Dermatitides", "Dermatitides, Digital", "bovine hairy footwart", "Dermatitides, digital", "digital Papillomatoses", "footwart, bovine hairy", "Digital Papillomatoses", "bovine hairy footwarts", "Digital Papillomatosis", "hairy footwart, bovine", "digital papillomatosis", "Papillomatoses, Digital", "papillomatosis, digital", "hairy footwarts, bovine", "Papillomatoses, digital", "Papillomatosis, Digital", "footwarts, bovine hairy", "Ovine digital dermatitis", "digital dermatitis, Ovine", "bovine digital dermatitis", "Ovine digital Dermatitides", "dermatitis, bovine digital", "digital dermatitis, bovine", "bovine digital Dermatitides", "digital Dermatitides, Ovine", "digital Dermatitides, bovine", "Dermatitides, bovine digital", "digital dermatitis in cattle", "papillomatous digital dermatitis", "Papillomatous Digital Dermatitis", "digital dermatitis, papillomatous", "Digital Dermatitis, Papillomatous", "papillomatous digital Dermatitides", "Papillomatous Digital Dermatitides", "Digital Dermatitides, Papillomatous", "digital Dermatitides, papillomatous"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "digital dermatitis in cattle", "shortest_name_length": 16}
{"curie": "MONDO:0011345", "names": ["Facial Dysmorphism, Selective Tooth Agenesis, and Choroid Calcification", "FACIAL DYSMORPHISM, SELECTIVE TOOTH AGENESIS, AND CHOROID CALCIFICATION", "facial dysmorphism, selective tooth agenesis, and choroid calcification"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "facial dysmorphism, selective tooth agenesis, and choroid calcification", "shortest_name_length": 71}
{"curie": "MONDO:0007738", "names": ["HSD", "CDMD", "SEDCJD", "Omani type", "Omani Type", "SED, Omani Type", "SDCD, CHST3 type", "Gollop Coates syndrome", "HUMEROSPINAL DYSOSTOSIS", "Humerospinal dysostosis", "humerospinal dysostosis", "Humero-spinal dysostosis", "Humero-Spinal Dysostosis", "humero-spinal dysostosis", "spondyloepiphyseal dysplasia", "Spondyloepiphyseal Dysplasia", "SED with Luxations, CHST3 Type", "CHST3-related skeletal dysplasia", "CHST3-Related Skeletal Dysplasia", "Kozlowski Celermajer tink syndrome", "Kozlowski Celermajer Tink syndrome", "spondyloepiphyseal dysplasia, Omani type", "Spondyloepiphyseal dysplasia, Omani type", "SPONDYLOEPIPHYSEAL DYSPLASIA, OMANI TYPE", "Omani type of spondyloepiphyseal dysplasia", "chondrodysplasia with multiple dislocations", "Chondrodysplasia with Multiple Dislocations", "Spondyloepiphyseal Dysplasia, CHST3-Related", "CHONDRODYSPLASIA WITH MULTIPLE DISLOCATIONS", "Humero-spinal dysostosis with congenital heart disease", "humero-spinal dysostosis with congenital heart disease", "bifurcation of distal humerus with oligoectro-syndactyly", "Bifurcation of distal humerus with oligoectro-syndactyly", "Carbohydrate sulfotransferase 3 related skeletal dysplasia", "SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS", "spondyloepiphyseal dysplasia with congenital JOINT dislocations", "Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations", "spondyloepiphyseal dysplasia with congenital joint dislocations", "Chondrodysplasia with congenital joint dislocations, CHST3 type", "Spondyloepiphyseal dysplasia with congenital joint dislocations", "chondrodysplasia with congenital joint dislocations, CHST3 type", "Carbohydrate sulfotransferase 3 related skeletal dysplasia (disorder)", "Spondyloepiphyseal dysplasia with congenital joint dyslocations CHST3 type", "Spondyloepiphyseal dysplasia with congenital joint dislocations (disorder)", "Spondyloepiphyseal dysplasia with congenital joint dyslocations, CHST3 type", "spondyloepiphyseal dysplasia with congenital joint dyslocations, CHST3 type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepiphyseal dysplasia with congenital joint dislocations", "shortest_name_length": 3}
{"curie": "MONDO:0019378", "names": ["lacrosse encephalitis", "encephalitis lacrosse", "Lacrosse encephalitis", "la Crosse encephalitis", "la crosse encephalitis", "LA CROSSE ENCEPHALITIS", "La Crosse encephalitis", "La Crosse Encephalitis", "La Crosse; encephalitis", "California Encephalitis", "California encephalitis", "Encephalitis california", "encephalitis; La Crosse", "Encephalitis, La Crosse", "Californian encephalitis", "encephalitis; California", "Encephalitis, California", "ENCEPHALITIS, CALIFORNIA", "LAC - La Crosse encephalitis", "CE - California encephalitis", "La Crosse virus encephalitis", "California virus encephalitis", "California Viral Encephalitis", "California viral encephalitis", "California meningoencephalitis", "Encephalitis, California Viral", "Viral Encephalitis, California", "Encephalitis, California, Viral", "meningoencephalitis; California", "California; encephalitis (viral)", "La Crosse encephalitis (disorder)", "La Crosse encephalitis (diagnosis)", "California encephalitis (diagnosis)", "California encephalitis virus disease", "La Crosse Encephalitis Virus Infection", "La Crosse virus infectious encephalitis", "California; meningoencephalitis (viral)", "California Encephalitis Virus Infection", "California encephalitis virus infection", "California meningoencephalitis virus disease", "La Crosse virus caused infectious encephalitis", "California serogroup virus neuroinvasive disease", "California encephalitis virus infection (disorder)", "Neuroinvasive California encephalitis virus infection", "California serogroup virus neuroinvasive disease (disorder)", "California encephalitis virus infection neuroinvasive disease", "Neuroinvasive California encephalitis virus infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "la Crosse encephalitis", "shortest_name_length": 21}
{"curie": "MONDO:0019746", "names": ["Cystinuria type B", "cystinuria type B", "Cystinuria, Type B", "CYSTINURIA, TYPE B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cystinuria type B", "shortest_name_length": 17}
{"curie": "MONDO:0044981", "names": ["pseudoallergy", "Substance pseudoallergy", "Pseudoallergy to substance", "pseudoallergy to substance", "Nonallergic hypersensitivity to substance", "Non-allergic hypersensitivity to substance", "Non-allergic hypersensitivity to substance (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudoallergy", "shortest_name_length": 13}
{"curie": "UMLS:C2981671", "names": ["Stage IB Ampulla of Vater Cancer", "Stage IB Ampulla of Vater Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Ampulla of Vater Cancer AJCC v7", "shortest_name_length": 32}
{"curie": "MONDO:0019560", "names": ["LET", "let", "tumid lupus erythematosus", "Tumid Lupus Erythematosus", "lupus erythematosus tumidus", "Lupus Erythematosus Tumidus", "Lupus erythematosus tumidus", "Intermittent cutaneous lupus", "intermittent cutaneous lupus", "Lupus erythematosus tumidus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lupus erythematosus tumidus", "shortest_name_length": 3}
{"curie": "MONDO:0003892", "names": ["Lung Acinar Adenocarcinoma", "lung acinar adenocarcinoma", "acinar lung adenocarcinoma", "acinar adenocarcinoma of lung", "Acinar Adenocarcinoma of Lung", "Acinar Adenocarcinoma of the Lung", "acinar adenocarcinoma of the lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acinar lung adenocarcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0021697", "names": ["Chlamydia", "chlamydial disease", "Chlamydial disease", "Chlamydia infection", "Chlamydia Infection", "chlamydia infection", "infection, Chlamydia", "Chlamydia infections", "chlamydia infections", "Infection, Chlamydia", "Chlamydia Infections", "Chlamydia; infection", "CHLAMYDIAL INFECTION", "chlamydial infection", "Chlamydial infection", "Chlamydial Infection", "CHLAMYDIAL INFECTIONS", "infection; chlamydial", "infections, Chlamydia", "Infections, Chlamydia", "chlamydial infections", "Chlamydial infections", "Chlamydophila Infection", "Chlamydial infection NOS", "Chlamydophila Infections", "Infection, Chlamydophila", "Chlamydophila infections", "chlamydia bacteria infection", "Chlamydia infectious disease", "chlamydia infectious disease", "Chlamydia disease or disorder", "Chlamydial disease (diagnosis)", "Chlamydial infection (disorder)", "Chlamydial infectious disorders", "Chlamydophila infectious disease", "Chlamydial infection (diagnosis)", "Chlamydial infection, unspecified", "Chlamydophila disease or disorder", "Chlamydia caused disease or disorder", "Chlamydophila caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chlamydia infectious disease", "shortest_name_length": 9}
{"curie": "MONDO:0000301", "names": ["Ocular myiasis", "ocular myiasis", "Ophthalmomyiasis", "ophthalmomyiasis", "Ophthalmic myiasis", "ophthalmic myiasis", "Myiasis, ophthalmic", "Oestrus ovis myiasis", "Oestrus ovis caused myiasis", "Infestation of eye caused by fly larvae", "Infestation of eye caused by fly larvae (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ophthalmomyiasis", "shortest_name_length": 14}
{"curie": "MONDO:0004927", "names": ["Timo cyst", "dacryocele", "Dacryocele", "Dacryocystocele", "dacryocystocele", "Dacryocystocoele", "Lacrimal mucocele", "Lacrimal Mucocele", "lacrimal mucocele", "Lacrimal mucocoele", "Lacrimal sac mucocele", "mucocele; lacrimal sac", "lacrimal sac; mucocele", "Lacrimal mucocele (disorder)", "lacrimal mucocele (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dacryocystocele", "shortest_name_length": 9}
{"curie": "MONDO:0010274", "names": ["TGCT1", "testicular germ cell tumor", "Testicular Germ Cell Tumor 1", "TESTICULAR GERM CELL TUMOR 1", "testicular germ cell tumor 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular germ cell tumor 1", "shortest_name_length": 5}
{"curie": "MONDO:0007504", "names": ["Escher Hirt syndrome", "Escher-Hirt syndrome", "Thickened earlobes-conductive deafness syndrome", "thickened earlobes-conductive deafness syndrome", "Thickened earlobe with conductive deafness syndrome", "Thickened earlobes-conductive hearing loss syndrome", "Thickened earlobe with conductive deafness syndrome (disorder)", "EARLOBES, THICKENED, WITH CONDUCTIVE DEAFNESS FROM INCUDOSTAPEDIAL ABNORMALITIES", "earlobes, thickened, with conductive deafness from incudostapedial abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thickened earlobes-conductive deafness syndrome", "shortest_name_length": 20}
{"curie": "MONDO:0017039", "names": ["drug or radiation exposure-related interstitial lung disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "drug or radiation exposure-related interstitial lung disease", "shortest_name_length": 60}
{"curie": "MONDO:0014335", "names": ["MSCCA", "microcephaly, progressive, seizures, and cerebral and cerebellar atrophy", "MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLAR ATROPHY", "microcephaly, progressive, with seizures and cerebral and cerebellar atrophy", "diffuse cerebral and cerebellar atrophy - intractable seizures - progressive microcephaly syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diffuse cerebral and cerebellar atrophy - intractable seizures - progressive microcephaly syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0339108", "names": ["Eyelid Epidermoid Papilloma", "Eyelid Squamous Cell Papilloma", "Epidermoid Papilloma of Eyelid", "Squamous cell papilloma of eyelid", "Squamous Cell Papilloma of Eyelid", "Epidermoid Papilloma of the Eyelid", "Squamous Cell Papilloma of the Eyelid", "Squamous cell papilloma of eyelid (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Squamous cell papilloma of eyelid", "shortest_name_length": 27}
{"curie": "MONDO:0013840", "names": ["COQ10D5", "primary coenzyme Q10 deficiency 5", "COENZYME Q10 DEFICIENCY, PRIMARY, 5", "coenzyme Q10 deficiency, primary, 5", "coenzyme Q10 deficiency, primary, type 5", "encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome", "shortest_name_length": 7}
{"curie": "UMLS:C3274709", "names": ["Contralateral Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Contralateral Breast Carcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0000819", "names": ["Anencephaly", "anencephaly", "ANENCEPHALY", "Anencephalus", "anencephalus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anencephaly", "shortest_name_length": 11}
{"curie": "MONDO:0012947", "names": ["MRD4", "autosomal dominant mental retardation 4", "Mental Retardation, Autosomal Dominant 4", "mental retardation, autosomal dominant 4", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 4", "autosomal dominant intellectual disability 4", "intellectual disability, autosomal dominant 4", "mental retardation, autosomal dominant type 4", "intellectual disability, autosomal dominant type 4", "autosomal dominant intellectual developmental disorder 4", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 4", "autosomal dominant non-syndromic intellectual disability 4", "KIRREL3 autosomal dominant non-syndromic intellectual disability", "autosomal dominant non-syndromic intellectual disability caused by mutation in KIRREL3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 4", "shortest_name_length": 4}
{"curie": "UMLS:C1136209", "names": ["Serogroup Y, Meningococcal Meningitis", "Meningococcal Meningitis, Serogroup Y", "Meningitis, Meningococcal, Serogroup Y"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meningitis, Meningococcal, Serogroup Y", "shortest_name_length": 37}
{"curie": "UMLS:C0334430", "names": ["Neuronevus", "Neuronaevus", "Neural Nevus", "Neuronevus (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neuronevus", "shortest_name_length": 10}
{"curie": "MONDO:0011915", "names": ["MVP2", "MMVP2", "mitral valve prolapse 2", "MITRAL VALVE PROLAPSE 2", "myxomatous mitral valve prolapse 2", "Myxomatous Mitral Valve Prolapse 2", "MYXOMATOUS MITRAL VALVE PROLAPSE 2", "mitral valve prolapse, myxomatous 2", "Mitral Valve Prolapse, Myxomatous 2", "MITRAL VALVE PROLAPSE, MYXOMATOUS 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitral valve prolapse, myxomatous 2", "shortest_name_length": 4}
{"curie": "MONDO:0001216", "names": ["Pulp Degeneration", "Pulp degeneration", "pulp degeneration", "degeneration; dental pulp", "dental pulp; degeneration", "Pulp degeneration (disorder)", "pulp degeneration (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulp degeneration", "shortest_name_length": 17}
{"curie": "MONDO:0000334", "names": ["Multinodular Goiter", "Multinodular goitre", "multinodular goitre", "Multinodular goiter", "multinodular goiter", "MULTINODULAR GOITER", "multinodular; goiter", "multinodular thyroid", "thyroid multinodular", "goiter, multinodular", "goiters multinodular", "struma; multinodular", "MULTINODULAR THYROID", "Goiter, multinodular", "Multiple thyroid nodules", "multiple nodules thyroid", "THYROID GOITER MULTINODULAR", "Thyroid goiter multinodular", "multiple nodules of thyroid", "Thyroid goitre multinodular", "Multinodular goiter (disorder)", "the thyroid had multiple nodules", "multiple nodules of thyroid (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multinodular goiter", "shortest_name_length": 19}
{"curie": "MONDO:0011098", "names": ["HPC1", "Prca1", "PRCA1", "prostate cancer 1", "PROSTATE CANCER, HEREDITARY, 1", "Prostate Cancer, Hereditary, 1", "prostate cancer, hereditary, 1", "RNASEL familial prostate cancer", "prostate cancer, hereditary, type 1", "familial prostate cancer caused by mutation in RNASEL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate cancer, hereditary, 1", "shortest_name_length": 4}
{"curie": "MONDO:0040501", "names": ["EDS 7B", "EDS VIIB", "EDSARTH2", "Ehlers-Danlos syndrome arthrochalasia type 2", "Ehlers-Danlos syndrome, arthrochalasia type, 2", "ehlers-danlos syndrome, arthrochalasia type, 2", "Ehlers-Danlos syndrome, type VIIb, Autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ehlers-danlos syndrome, arthrochalasia type, 2", "shortest_name_length": 6}
{"curie": "MONDO:0023288", "names": ["Green Sandford Davison syndrome", "green sandford davison syndrome", "renal and anogenital malformations with syndactyly", "anal anomalies, renal tract abnormalities, genital malformations, and syndactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "green sandford davison syndrome", "shortest_name_length": 31}
{"curie": "MONDO:0004794", "names": ["exposure keratitis", "Exposure keratitis", "Exposure keratopathy", "lagophthalmic keratitis", "Lagophthalmic keratitis", "Exposure keratoconjunctivitis", "exposure keratoconjunctivitis", "exposure; keratoconjunctivitis", "Exposure keratoconjunctivitis (disorder)", "exposure keratoconjunctivitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exposure keratitis", "shortest_name_length": 18}
{"curie": "EFO:0010269", "names": ["amenorrhea\"@e"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amenorrhea\"@e", "shortest_name_length": 13}
{"curie": "MONDO:0005269", "names": ["CAROTID ARTERY DISEASE", "Carotid Artery Disease", "Carotid artery disease", "carotid artery disease", "Artery Disease, Carotid", "carotid artery disorder", "Carotid Artery Disorder", "Carotid Artery Diseases", "carotid arterial disease", "Carotid Arterial Disease", "carotid artery disorders", "arteries carotid disease", "Artery Disorder, Carotid", "Carotid Artery Disorders", "Artery Diseases, Carotid", "Carotid artery--Diseases", "of carotid artery disease", "Disease of carotid artery", "Carotid Arterial Diseases", "Arterial Disease, Carotid", "Disorders, Carotid Artery", "Artery Disorders, Carotid", "Carotid artery disease NOS", "Arterial Diseases, Carotid", "disorder of carotid artery", "Disorder of carotid artery", "Abnormality of carotid artery", "carotid artery segment disease", "disease of carotid artery segment", "disorder of carotid artery segment", "Disorder of carotid artery (disorder)", "Abnormality of external carotid artery", "carotid artery segment disease or disorder", "disease or disorder of carotid artery segment"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carotid artery disorder", "shortest_name_length": 22}
{"curie": "MONDO:0016238", "names": ["SFT", "hemangiopericytoma", "Hemangiopericytoma", "Haemangiopericytoma", "Solitary Fibrous Tumor", "Solitary fibrous tumor", "solitary fibrous tumor", "Submesothelial Fibroma", "submesothelial fibroma", "Localized fibrous tumor", "localized fibrous tumor", "Fibrous Tumor, Solitary", "solitary fibrous tumour", "Solitary Fibrous Tumors", "Solitary fibrous tumour", "Tumor, Solitary Fibrous", "Localized Fibrous Tumor", "Fibrous Tumors, Solitary", "Tumors, Solitary Fibrous", "Localised fibrous tumour", "Solitary Fibrous Tumor, NOS", "localized fibrous mesothelioma", "Localized fibrous mesothelioma", "Localized Fibrous Mesothelioma", "Localised fibrous mesothelioma", "solitary fibrous tumor/hemangiopericytoma", "Solitary Fibrous Tumor, Not Otherwise Specified", "Solitary fibrous tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "solitary fibrous tumor", "shortest_name_length": 3}
{"curie": "MONDO:0004549", "names": ["SUBEROSIS", "suberosis", "Suberosis", "cork workers lung", "cork worker's lung", "cork handlers' lung", "cork-handlers' lung", "Cork-handlers' lung", "Suberosis (disorder)", "suberosis (diagnosis)", "Corkhandler's disease", "Cork-handlers' disease", "cork-handlers' disease", "corkworker's disease or lung", "Corkworker's disease or lung", "corkhandler's disease or lung", "Corkhandler's disease or lung", "Cork-handlers' disease or lung", "cork-handlers' disease or lung", "hypersensitivity; pneumonitis, corkhandler's", "pneumonitis; hypersensitivity, corkhandler's", "disease (or disorder); corkhandler's or corkworker's"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cork-handlers' disease", "shortest_name_length": 9}
{"curie": "UMLS:C5418568", "names": ["Locally Advanced Gallbladder Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Gallbladder Carcinoma", "shortest_name_length": 38}
{"curie": "MONDO:0016838", "names": ["Del(16)(q24.3)", "monosomy 16q24.3", "Monosomy 16q24.3", "16q24.3 microdeletion syndrome", "16q24.3 microdeletion syndrome (disorder)", "chromosome 16q24.3 microdeletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "16q24.3 microdeletion syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0014501", "names": ["EOMD", "macular degeneration, early-onset", "MACULAR DEGENERATION, EARLY-ONSET"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macular degeneration, early-onset", "shortest_name_length": 4}
{"curie": "UMLS:C0333161", "names": ["Pseudocyst", "PSEUDOCYST", "pseudocyst", "pseudocysts", "Pseudocyst, NOS", "Pseudocyst (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pseudocyst", "shortest_name_length": 10}
{"curie": "MONDO:0020950", "names": ["EYE INFECT VIRAL", "VIRAL EYE INFECT", "viral eye infection", "eye viral infection", "Eye infection viral", "Viral Eye Infection", "Viral eye infection", "OCULAR INFECT VIRAL", "eye infection viral", "eye viral infections", "eye infections viral", "Infection, Viral Eye", "Viral Eye Infections", "Eye Infection, Viral", "viral eye infections", "Infections, Viral Eye", "Eye Infections, Viral", "Viral Ocular Infection", "Eye infection viral NOS", "Ocular Infection, Viral", "Infection, Viral Ocular", "Viral eye infection NOS", "Viral Ocular Infections", "Ocular Infections, Viral", "Infections, Viral Ocular", "Viral ophthalmic infection", "Viral eye infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "viral eye infection", "shortest_name_length": 16}
{"curie": "UMLS:C2930879", "names": ["Subacute cerebellar degeneration", "Cerebellar degeneration, subacute"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebellar degeneration, subacute", "shortest_name_length": 32}
{"curie": "UMLS:C1332542", "names": ["Benign Corpus Uteri Mixed Tumor", "Benign Uterine Body Mixed Tumor", "Benign Uterine Corpus Mixed Tumor", "Benign Corpus Uteri Mixed Neoplasm", "Benign Mixed Tumor of Corpus Uteri", "Benign Uterine Body Mixed Neoplasm", "Benign Mixed Tumor of Uterine Body", "Benign Mixed Tumor of Body of Uterus", "Benign Mixed Tumor of Uterine Corpus", "Benign Mixed Neoplasm of Corpus Uteri", "Benign Mixed Neoplasm of Uterine Body", "Benign Mixed Tumor of the Uterine Body", "Benign Mixed Tumor of the Corpus Uteri", "Benign Mixed Neoplasm of Uterine Corpus", "Benign Mixed Neoplasm of Body of Uterus", "Benign Mixed Tumor of the Uterine Corpus", "Benign Mixed Tumor of the Body of Uterus", "Benign Mixed Neoplasm of the Uterine Body", "Benign Mixed Neoplasm of the Corpus Uteri", "Benign Mixed Neoplasm of the Uterine Corpus", "Benign Mixed Neoplasm of the Body of Uterus", "Benign Uterine Corpus Mixed Epithelial and Mesenchymal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Uterine Corpus Mixed Epithelial and Mesenchymal Neoplasm", "shortest_name_length": 31}
{"curie": "UMLS:C0279590", "names": ["L2 adult ALL", "ALL, adult L2", "adult ALL, L2", "ALL, L2 adult", "L2 Acute Lymphoblastic Leukemia", "L2 adult acute lymphocytic leukemia", "L2 lymphocytic leukemia, acute adult", "L2 acute lymphocytic leukemia, adult", "acute lymphocytic leukemia, adult L2", "adult acute lymphocytic leukemia, L2", "L2 adult acute lymphoblastic leukemia", "Adult L2 Acute Lymphoblastic Leukemia", "leukemia, adult acute lymphocytic , L2", "adult acute lymphoblastic leukemia, L2", "L2 lymphoblastic leukemia, acute adult", "acute lymphoblastic leukemia, adult L2", "L2 acute lymphoblastic leukemia, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult L2 Acute Lymphoblastic Leukemia", "shortest_name_length": 12}
{"curie": "UMLS:C5668174", "names": ["Mesenchymal Cardiac Hamartoma", "Cardiac Mesenchymal Hamartoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiac Mesenchymal Hamartoma", "shortest_name_length": 29}
{"curie": "UMLS:C4722404", "names": ["ARCH", "Age-related Clonal Hematopoiesis", "Age-Related Clonal Hematopoiesis", "Age related Clonal Hematopoiesis", "Clonal Hematopoiesis, Age-related", "Hematopoiesis, Age-related Clonal", "ARCH Age-related Clonal Hematopoiesis", "ARCH Age related Clonal Hematopoiesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Age-Related Clonal Hematopoiesis", "shortest_name_length": 4}
{"curie": "MONDO:0005275", "names": ["pneumopathy", "Pneumopathy", "LUNG DISEASE", "Lung disease", "Lung Disease", "Disease;lung", "lung disease", "lung; disease", "LUNG DISORDER", "disorder lung", "DISORDER LUNG", "lung disorder", "lung diseases", "Lung Diseases", "Lung diseases", "Lung Disorder", "Disease, Lung", "Disorder lung", "Lung disorder", "diseases lungs", "Diseases, Lung", "Lung Disorders", "disorders lung", "lung disorders", "Lungs--Diseases", "disease of lung", "disorder of lung", "Lung disease NOS", "Disorder of lung", "Disorder of Lung", "PULMONARY DISEASE", "Unusal lung shape", "Pulmonary Disease", "Lung disorder NOS", "pulmonary disease", "Pulmonary disease", "pulmonary disorder", "diseases pulmonary", "Pulmonary Disorder", "Pulmonary disorder", "Lung disorder, NOS", "PULMONARY DISORDER", "pulmonary diseases", "Disease, Pulmonary", "Disorder pulmonary", "DISORDER PULMONARY", "Pulmonary Diseases", "Diseases, Pulmonary", "pulmonary; disorder", "PULMONARY DISORDERS", "disorders pulmonary", "LUNG DISORDER (NOS)", "pulmonary disorders", "Pulmonary Disorders", "Disease of lung, NOS", "diseases of the lung", "DISEASES OF THE LUNG", "Abnormally shaped lung", "Pulmonary disease, NOS", "lung disease or disorder", "Abnormal lung morphology", "Abnormality of the lungs", "disease (or disorder); lung", "disease or disorder of lung", "Disorder of lung (disorder)", "pulmonary disease (diagnosis)", "Abnormality of lung structure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung disorder", "shortest_name_length": 11}
{"curie": "MONDO:0013411", "names": ["CTPP2", "CTRCT16", "Zonular cataract", "Lamellar cataract", "cataract 16 multiple types", "posterior polar cataract 2", "congenital zonular cataract", "Congenital zonular cataract", "cataract 16, multiple types", "CATARACT 16, MULTIPLE TYPES", "CATARACT, POSTERIOR POLAR, 2", "Congenital lamellar cataract", "Cataract, Posterior Polar, 2", "cataract, posterior polar, 2", "cataract, congenital lamellar", "CATARACT, CONGENITAL LAMELLAR", "Cataract, congenital, lamellar", "Congenital zonular cataract (disorder)", "Congenital lamellar cataract (disorder)", "congenital zonular cataract (diagnosis)", "CRYAB early-onset non-syndromic cataract", "early-onset non-syndromic cataract caused by mutation in CRYAB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 16 multiple types", "shortest_name_length": 5}
{"curie": "UMLS:C0752244", "names": ["cyst; Rathke", "Rathke; cyst", "SUPRASELLAR CYST", "Suprasellar Cyst", "suprasellar cyst", "Rathke Cleft Cyst", "Rathke pouch cyst", "Cyst, Suprasellar", "rathke cleft cyst", "Suprasellar Cysts", "Rathke Pouch Cyst", "Rathke Cleft Cysts", "Cysts, Suprasellar", "Cyst, Rathke Cleft", "cleft cyst rathkes", "Cleft Cyst, Rathke", "Rathkes Cleft Cyst", "Rathke's Cleft Cyst", "Cysts, Rathke Cleft", "Rathke's cleft cyst", "Rathke's Pouch Cyst", "cleft cyst rathke's", "cyst; pouch, Rathke", "pouch, Rathke; cyst", "rathke's cleft cyst", "Rathkes Cleft Cysts", "Rathke's pouch cyst", "Cleft Cyst, Rathke's", "Cyst, Rathke's Cleft", "Rathke's Cleft Cysts", "Cleft Cysts, Rathke's", "Cyst of Rathke's Pouch", "Cyst of Rathke's pouch", "Rathke's pouch cyst (disorder)", "Rathke's pouch cyst (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rathke Cleft Cysts", "shortest_name_length": 12}
{"curie": "MONDO:0003827", "names": ["Transient Hypogammaglobulinemia", "transient hypogammaglobulinemia", "hypogammaglobulinemia; transient", "transient; hypogammaglobulinemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transient hypogammaglobulinemia", "shortest_name_length": 31}
{"curie": "UMLS:C0686584", "names": ["Leukemia in remission", "Leukemia in Remission", "leukemia in remission", "Leukaemia in remission", "Leukemia (in Remission)", "Leukemia (in remission)", "Leukemia, NOS, in remission", "Leukemia NOS (in remission)", "Leukaemia, NOS, in remission", "Leukaemia NOS (in remission)", "Leukemia in remission (disorder)", "Unspecified leukemia in remission", "leukemia in remission (diagnosis)", "Unspecified leukemia, in remission", "Unspecified leukaemia in remission", "Leukemia, unspecified, in remission", "Leukaemia, unspecified, in remission"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leukemia in remission", "shortest_name_length": 21}
{"curie": "UMLS:C0001577", "names": ["Adnexitis", "adnexitis", "ADNEXITIS", "Uterine adnexitis", "Uterine Adnexitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adnexitis", "shortest_name_length": 9}
{"curie": "UMLS:C0521607", "names": ["peritoneal fibrosis", "Peritoneal fibrosis", "Peritoneal Fibrosis", "Peritoneal Fibroses", "Fibrosis, Peritoneal", "Fibroses, Peritoneal", "Fibrosis of peritoneum", "Peritoneal Fibrosing Syndrome", "Fibrosing Syndrome, Peritoneal", "Syndrome, Peritoneal Fibrosing", "Peritoneal Fibrosing Syndromes", "Syndromes, Peritoneal Fibrosing", "Fibrosing Syndromes, Peritoneal", "Fibrosis of peritoneum (disorder)", "Fibrosis of peritoneal serous membrane"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peritoneal Fibrosis", "shortest_name_length": 19}
{"curie": "UMLS:C0151536", "names": ["BRONCHOSTENOSIS", "Bronchostenosis", "bronchostenosis", "BRONCHUS, STENOSIS", "stenosis; bronchus", "STENOSIS BRONCHIAL", "bronchus; stenosis", "Bronchial stenosis", "bronchial stenosis", "Stenosis bronchial", "Stenosis of bronchus", "bronchial stenosis (diagnosis)", "Stenosis of bronchus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stenosis of bronchus", "shortest_name_length": 15}
{"curie": "UMLS:C1378107", "names": ["Stage III Fallopian Tube Cancer", "FIGO Stage III Fallopian Tube Carcinoma", "Stage III Fallopian Tube Cancer AJCC v6", "Fallopian Tube Cancer Stage III AJCC v6", "AJCC Stage III Fallopian Tube Cancer v6", "FIGO Stage III Carcinoma of Fallopian Tube", "FIGO Stage III Carcinoma of the Fallopian Tube", "FIGO Stage III Carcinoma of the Fallopian Tube AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Stage III Carcinoma of the Fallopian Tube", "shortest_name_length": 31}
{"curie": "MONDO:0013060", "names": ["PARK14", "Parkinson's disease 14", "Dystonia-Parkinsonism Adult-Onset", "Adult-onset dystonia-parkinsonism", "dystonia-Parkinsonism Adult-onset", "Adult-onset dystonia parkinsonism", "Dystonia-Parkinsonism, Adult-Onset", "dystonia-Parkinsonism, adult-onset", "DYSTONIA-PARKINSONISM, ADULT-ONSET", "adult-onset dystonia - parkinsonism", "PLA2G6-related dystonia-parkinsonism", "Dystonia parkinsonism Paisan-Ruiz type", "dystonia-parkinsonism, Paisan-Ruiz type", "Dystonia-parkinsonism, Paisan-Ruiz type", "autosomal recessive Parkinson disease 14", "Parkinson disease 14, autosomal recessive", "Parkinson Disease 14, Autosomal Recessive", "PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE", "autosomal recessive Parkinson's disease 14", "Adult-onset dystonia parkinsonism (disorder)", "autosomal recessive Parkinson disease type 14", "PLA2G6 hereditary late onset Parkinson disease", "PLA2G6 (phospholipase A2 group VI) related dystonia parkinsonism", "hereditary late onset Parkinson disease caused by mutation in PLA2G6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive Parkinson disease 14", "shortest_name_length": 6}
{"curie": "MONDO:0002698", "names": ["Gonadoblastoma, male", "testis gonadoblastoma", "gonadoblastoma of testis", "Testicular Gonadoblastoma", "testicular gonadoblastoma", "Testicular gonadoblastoma", "testicular gonadoblastoma (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular gonadoblastoma", "shortest_name_length": 20}
{"curie": "MONDO:0007913", "names": ["low density lipoprotein, variation in molecular weight of", "LOW DENSITY LIPOPROTEIN, VARIATION IN MOLECULAR WEIGHT OF", "LOW density lipoprotein, variation in molecular weight OF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "low density lipoprotein, variation in molecular weight of", "shortest_name_length": 57}
{"curie": "MONDO:0019935", "names": ["isochromosome Y", "Isochromosome type Y"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isochromosome Y", "shortest_name_length": 15}
{"curie": "UMLS:C0751522", "names": ["Subclinical Status Epilepticus", "Status Epilepticus, Subclinical", "Electrographic Status Epilepticus", "Status Epilepticus, Electrographic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Status Epilepticus, Subclinical", "shortest_name_length": 30}
{"curie": "UMLS:C3838947", "names": ["Invasive Micropapillary Breast Carcinoma", "Invasive Breast Micropapillary Carcinoma", "Invasive micropapillary carcinoma of breast", "Infiltrating Micropapillary Breast Carcinoma", "Invasive micropapillary carcinoma of breast (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Invasive micropapillary carcinoma of breast", "shortest_name_length": 40}
{"curie": "UMLS:C5401226", "names": ["Metastatic Malignant Skin Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Malignant Skin Neoplasm", "shortest_name_length": 34}
{"curie": "UMLS:C0854466", "names": ["Implant expulsion", "Expulsion of implant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Expulsion of implant", "shortest_name_length": 17}
{"curie": "UMLS:C1511235", "names": ["Body Fluid Leakage", "Body Fluid Spillage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Body Fluid Leakage", "shortest_name_length": 18}
{"curie": "MONDO:0013834", "names": ["UVSS3", "UV-SENSITIVE SYNDROME 3", "UV-sensitive syndrome 3", "UV-Sensitive Syndrome 3", "UVSSA UV-sensitive syndrome", "UV-sensitive syndrome type 3", "UV-sensitive syndrome caused by mutation in UVSSA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "UV-sensitive syndrome 3", "shortest_name_length": 5}
{"curie": "UMLS:C3160869", "names": ["Metastatic Transitional Cell Cancer", "Metastatic Transitional Cell Carcinoma", "Transitional cell carcinoma metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transitional cell carcinoma metastatic", "shortest_name_length": 35}
{"curie": "UMLS:C2983712", "names": ["Breast Cancer by AJCC v6 Stage", "Breast Carcinoma by AJCC v6 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Cancer by AJCC v6 Stage", "shortest_name_length": 30}
{"curie": "UMLS:C4054155", "names": ["Primary Collapsing Glomerulopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Collapsing Glomerulopathy", "shortest_name_length": 33}
{"curie": "MONDO:0001969", "names": ["45,X/46,XY MGD", "45,X0/46,XY MGD", "mosaicism 45,x/46,xy", "45, X/46, XY mosaicism", "Mosaicism 45, X; 46, XY", "mixed gonadal dysgenesis", "Mixed Gonadal Dysgenesis", "Mixed gonadal dysgenesis", "gonadal dysgenesis mixed", "Gonadal Dysgenesis, Mixed", "mosaicism 45,x/46,xy (diagnosis)", "Mixed gonadal dysgenesis syndrome", "45,X/46,XY Mixed Gonadal Dysgenesis", "Mixed gonadal dysgenesis (disorder)", "45,X/46,XY mixed gonadal dysgenesis", "45,X0/46,XY mixed gonadal dysgenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed gonadal dysgenesis", "shortest_name_length": 14}
{"curie": "UMLS:C1541332", "names": ["Adult Acute Myeloid Leukemia with t(16;16)(p13;q22)", "adult acute myeloid leukemia with t(16;16)(p13;q22)", "Adult Acute Myeloid Leukemia with t(16;16)(p13.1;q22); CBFB-MYH11", "Acute Myeloid Leukemia (AML) with t(16;16)(p13.1;q22); CBFB-MYH11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Acute Myeloid Leukemia with t(16;16)(p13.1;q22); CBFB-MYH11", "shortest_name_length": 51}
{"curie": "MONDO:0011842", "names": ["HDDD", "FTDU", "FTLDU", "FTLD-TDP, GRN-RELATED", "FTLD-TDP, GRN-related", "aphasia, primary progressive", "FRONTOTEMPORAL DEMENTIA, UBIQUITIN-POSITIVE", "frontotemporal dementia, ubiquitin-positive", "dementia, hereditary dysphasic disinhibition", "DEMENTIA, HEREDITARY DYSPHASIC DISINHIBITION", "frontotemporal dementia with TDP43 inclusions, GRN-related", "FRONTOTEMPORAL DEMENTIA WITH TDP43 INCLUSIONS, GRN-RELATED", "Grn-related frontotemporal lobar degeneration with Tdp43 inclusions", "GRN-related frontotemporal lobar degeneration with Tdp43 inclusions", "FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED", "frontotemporal lobar degeneration with ubiquitin-positive inclusions", "FRONTOTEMPORAL LOBAR DEGENERATION WITH UBIQUITIN-POSITIVE INCLUSIONS", "frontotemporal lobar degeneration with TDP43 inclusions, GRN-related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "GRN-related frontotemporal lobar degeneration with Tdp43 inclusions", "shortest_name_length": 4}
{"curie": "MONDO:0005101", "names": ["uc", "Colitis Gravis", "Colitis gravis", "Colitis ulcerosa", "Ulcerative colitis", "Colitis Ulcerative", "Colitis ulcerative", "Ulcerative Colitis", "ulcerative colitis", "colitis ulcerative", "ULCERATIVE COLITIS", "Colitis;ulcerative", "COLITIS ULCERATIVE", "COLITIS, ULCERATIVE", "colitis; ulcerative", "ulcerative; colitis", "Colitis gravis, NOS", "Colitis, Ulcerative", "Ulcerative colitis, NOS", "UC - Ulcerative colitis", "PROCTOCOLITIS IDIOPATHIC", "Idiopathic proctocolitis", "idiopathic proctocolitis", "Idiopathic Proctocolitis", "Proctocolitis idiopathic", "Proctocolitis, idiopathic", "ulcerative colitis (disease)", "ulcerative proctosigmoiditis", "left-sided ulcerative colitis", "Ulcerative colitis (disorder)", "Left-sided ulcerative colitis", "ulcerative colitis (diagnosis)", "Ulcerative colitis, unspecified", "Chronic left-sided ulcerative colitis", "ulcerative left-sided colitis chronic", "Left-sided ulcerative (chronic) colitis", "left-sided ulcerative colitis (diagnosis)", "INFLAMMATORY BOWEL DISEASE ULCERATIVE COLITIS", "Chronic left-sided ulcerative colitis (disorder)", "Chronic left-sided ulcerative colitis (diagnosis)", "Ulcerative colitis as main diagnosis for the colon", "Inflammatory Bowel Disease, Ulcerative Colitis Type", "Ulcerative colitis as reason for lower g.i. examination"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ulcerative colitis", "shortest_name_length": 2}
{"curie": "UMLS:C5206836", "names": ["Retropharyngeal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retropharyngeal Neoplasm", "shortest_name_length": 24}
{"curie": "UMLS:C1336864", "names": ["Rectal Anaplastic Carcinoma", "carcinoma simplex of rectum", "anaplastic carcinoma of rectum", "Anaplastic Carcinoma of Rectum", "Undifferentiated Rectal Cancer", "carcinoma simplex of the rectum", "Carcinoma Simplex of the Rectum.", "rectal, carcinoma simplex of the", "rectum, carcinoma simplex of the", "Rectal Undifferentiated Carcinoma", "Undifferentiated Rectal Carcinoma", "Anaplastic Carcinoma of the Rectum", "undifferentiated carcinoma of rectum", "Undifferentiated Carcinoma of Rectum", "carcinoma simplex of rectum (diagnosis)", "Undifferentiated Carcinoma of the Rectum", "anaplastic carcinoma of rectum (diagnosis)", "undifferentiated carcinoma of rectum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anaplastic Carcinoma of the Rectum", "shortest_name_length": 27}
{"curie": "MONDO:0009303", "names": ["Goodpasture", "anti gbm disease", "Anti-GMB disease", "Anti-GBM Disease", "anti-GBM disease", "Anti-GBM disease", "Anti GBM Disease", "Anti-GBM syndrome", "anti-GBM syndrome", "Goodpasture disease", "goodpasture syndrome", "Goodpasture syndrome", "pneumorenal syndrome", "GOODPASTURE SYNDROME", "PNEUMORENAL SYNDROME", "Goodpasture Syndrome", "goodpasture's disease", "good posture syndrome", "Goodpasture's disease", "SYNDROME GOOD PASTURE", "good pasture syndrome", "goodpastures syndrome", "Syndrome, Goodpasture", "Goodpastures Syndrome", "Syndrome Goodpasture's", "Goodpasture's Syndrome", "GOODPASTURE'S SYNDROME", "SYNDROME GOOD POSTURES", "goodpasture's syndrome", "Goodpasture's syndrome", "good pastures syndrome", "Syndrome, Goodpasture's", "goodpastures's syndrome", "pulmonary renal syndrome", "Pulmonary-renal syndrome", "Pulmonary renal syndrome", "renal pulmonary syndrome", "pulmonary renal syndromes", "lung purpura with nephritis", "Lung Purpura with Nephritis", "Goodpasture's syndrome (disorder)", "Goodpasture's syndrome (diagnosis)", "Pulmonary renal syndrome (disorder)", "Lung Purpura with Glomerulonephritis", "Lung purpura with nephritis syndrome", "pulmonary; renal syndrome (Goodpasture)", "syndrome; pulmonary-renal (Goodpasture)", "Antiglomerular basement membrane disease", "Anti-Glomerular Basement Membrane Disease", "Anti Glomerular Basement Membrane Disease", "glomerulonephritis - pulmonary hemorrhage", "Glomerulonephritis - pulmonary hemorrhage", "Anti-glomerular basement membrane disease", "anti-glomerular basement membrane disease", "Hemorrhagic pneumonia and glomerulonephritis", "Pulmonary hemorrhage with glomerulonephritis", "Hemorrhagic pneumonia AND glomerulonephritis", "Anti-GBM nephritis with pulmonary hemorrhage", "Haemorrhagic pneumonia AND glomerulonephritis", "Pulmonary haemorrhage with glomerulonephritis", "Anti-GBM nephritis with pulmonary haemorrhage", "Haemorrhagic pneumonia and glomerulonephritis", "Pulmonary hemosiderosis with glomerulonephritis", "Pulmonary haemosiderosis with glomerulonephritis", "anti-glomerular basement membrane antibody disease", "Anti-glomerular basement membrane antibody disease", "Anti GBM - Antiglomerular basement membrane disease", "Anti GBM - antiglomerular basement membrane disease", "Anti-glomerular basement membrane disease (disorder)", "rapidly progressive glomerulonephritis with pulmonary hemorrhage", "Rapidly progressive glomerulonephritis with pulmonary hemorrhage", "Anti-glomerular basement membrane antibody glomerulonephritis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anti-glomerular basement membrane disease", "shortest_name_length": 11}
{"curie": "UMLS:C4687506", "names": ["Stage I Malignant Thymic Germ Cell Tumor", "Stage I Malignant Mediastinal Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Malignant Mediastinal Germ Cell Tumor", "shortest_name_length": 40}
{"curie": "MONDO:0013130", "names": ["MCOP4", "isolated microphthalmia 4", "Microphthalmia, Isolated 4", "MICROPHTHALMIA, ISOLATED 4", "microphthalmia, isolated 4", "GDF6 isolated microphthalmia", "isolated microphthalmia type 4", "microphthalmia, isolated type 4", "isolated microphthalmia caused by mutation in GDF6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated microphthalmia 4", "shortest_name_length": 5}
{"curie": "UMLS:C0853402", "names": ["Exposure to poisonous plant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Exposure to poisonous plant", "shortest_name_length": 27}
{"curie": "MONDO:0003775", "names": ["lateral ventricle meningioma", "Lateral Ventricle Meningioma", "Meningioma of Lateral Ventricle", "meningioma of lateral ventricle", "meningioma of the Lateral Ventricle", "Meningioma of the Lateral Ventricle", "meningioma of the lateral ventricle", "telencephalic ventricle meningioma (disease)", "meningioma (disease) of telencephalic ventricle"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lateral ventricle meningioma", "shortest_name_length": 28}
{"curie": "UMLS:C2986965", "names": ["Stage IIIC2 Uterine Corpus Cancer", "Stage IIIC2 Uterine Corpus Cancer AJCC v7", "Stage IIIC2 Uterine (including Endometrial) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC2 Uterine Corpus Cancer AJCC v7", "shortest_name_length": 33}
{"curie": "UMLS:C1697981", "names": ["Anal necrosis", "anal necrosis", "Anal Necrotic Lesion", "anal necrosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anal Necrotic Lesion", "shortest_name_length": 13}
{"curie": "UMLS:C0334571", "names": ["Fibromatous epulis", "Peripheral Odontogenic Fibroma", "Peripheral odontogenic fibroma", "fibroma; odontogenic, peripheral", "odontogenic; fibroma, peripheral", "Peripheral odontogenic fibroma (disorder)", "Peripheral odontogenic fibroma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peripheral Odontogenic Fibroma", "shortest_name_length": 18}
{"curie": "MONDO:0008338", "names": ["DA8", "CPSFS1A", "CPSKF1A", "DA8, FORMERLY", "AUTOSOMAL DOMINANT", "distal arthrogryposis type 8", "PTERYGIUM SYNDROME, MULTIPLE", "arthrogryposis distal type 8", "Distal arthrogryposis type 8", "Arthrogryposis, Distal, Type 8", "arthrogryposis, distal, type 8", "ARTHROGRYPOSIS, DISTAL, TYPE 8, FORMERLY", "Autosomal dominant multiple pterygium syndrome", "multiple pterygium syndrome autosomal dominant", "multiple pterygium syndrome, autosomal dominant", "Multiple Pterygium Syndrome, Autosomal Dominant", "MULTIPLE PTERYGIUM SYNDROME, AUTOSOMAL DOMINANT", "Pterygium Syndrome, Multiple, Autosomal Dominant", "pterygium syndrome, multiple, autosomal dominant", "Autosomal dominant multiple pterygium syndrome (disorder)", "Autosomal dominant multiple pterygium syndrome (diagnosis)", "CONTRACTURES, PTERYGIA, AND VARIABLE SKELETAL FUSIONS SYNDROME 1A", "CONTRACTURES, PTERYGIA, AND SPONDYLOCARPOTARSAL FUSION SYNDROME 1A", "contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A", "contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A", "shortest_name_length": 3}
{"curie": "UMLS:C0472377", "names": ["Basal ganglia bleeding", "basal ganglia hemorrhage", "Basal Ganglia Hemorrhage", "Basal ganglia hemorrhage", "Hemorrhage, Basal Ganglia", "Basal ganglia haemorrhage", "Basal Ganglionic Hemorrhage", "Ganglionic Hemorrhage, Basal", "Hemorrhage, Basal Ganglionic", "Basal ganglia hemorrhage (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Basal Ganglia Hemorrhage", "shortest_name_length": 22}
{"curie": "MONDO:0100415", "names": ["AML, FLT3-ITD", "AML, FLT3 ITD", "AML, FLT3-ITD Mutation", "AML, FLT3/ITD Mutation", "AML, Activating FLT3-ITD Mutation", "AML, FLT3-ITD Activating Mutation", "AML, FLT3 internal tandem duplication", "AML, Activating FLT3-ITD Gene Mutation", "Acute Myeloid Leukemia (AML) with FLT3/ITD", "Acute Myeloid Leukemia with FLT3/ITD Mutation", "acute myeloid leukemia, FLT3 internal tandem duplication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, FLT3 internal tandem duplication", "shortest_name_length": 13}
{"curie": "MONDO:0009379", "names": ["HBLRR", "Rotor", "Rotor syndrome", "rotor syndrome", "Rotor Syndrome", "ROTOR SYNDROME", "syndrome rotor", "Syndrome, Rotor", "rotors syndrome", "rotor's syndrome", "Rotor's syndrome", "rotor's syndromes", "Hyperbilirubinemia type I", "Rotor syndrome (disorder)", "Hyperbilirubinaemia type I", "Rotor's syndrome (diagnosis)", "Rotor-type hyperbilirubinemia", "Rotor Type Hyperbilirubinemia", "hyperbilirubinemia, ROTOR type", "Hyperbilirubinemia, Rotor type", "HYPERBILIRUBINEMIA, IDIOPATHIC", "Hyperbilirubinemia, Rotor Type", "HYPERBILIRUBINEMIA, ROTOR TYPE", "hyperbilirubinemia, Rotor type", "hyperbilirubinemia, rotor type, digenic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rotor syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0265547", "names": ["Hemimelia", "Limb reduction defect", "limb reduction defect", "defect limbs reduction", "defects limb reduction", "Limb reduction deformity", "Limb reduction defect, NOS", "Reduction deformity of limb", "Reduction defect of limb NOS", "Longitudinal deficiency of limb", "Reduction deformity of limb, NOS", "congenital reduction defect of limb", "Longitudinal deficiency of limb, NOS", "Reduction defects of unspecified limb", "Reduction deformities, unspecified limb", "Longitudinal deficiency of limb (disorder)", "congenital reduction defect of limb (diagnosis)", "Reduction deformities, unspecified limb, congenital", "Longitudinal reduction deformity of unspecified limb(s)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Longitudinal deficiency of limb", "shortest_name_length": 9}
{"curie": "MONDO:0010019", "names": ["Secretory IgA deficiency", "Iga Deficiency, Secretory", "IgA deficiency, secretory", "IgA DEFICIENCY, SECRETORY", "Secretory piece deficiency", "secretory piece deficiency", "Secretory Component Deficiency", "secretory component deficiency", "SECRETORY COMPONENT DEFICIENCY", "Secretory component deficiency", "Secretory piece deficiency (disorder)", "secretory piece deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secretory component deficiency", "shortest_name_length": 24}
{"curie": "MONDO:0006993", "names": ["failure heart systolic", "Systolic Heart Failure", "heart failure systolic", "Systolic heart failure", "systolic heart failure", "Heart Failure, Systolic", "Systolic Heart Failures", "Heart Failures, Systolic", "Systolic heart failure (disorder)", "Systolic heart failure, unspecified", "Heart Failure, Reduced Ejection Fraction", "Unspecified systolic (congestive) heart failure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "systolic heart failure", "shortest_name_length": 22}
{"curie": "UMLS:C0343239", "names": ["neonatal hypotonia", "benign congenital hypotonia", "Benign congenital hypotonia", "Benign Congenital Hypotonia", "hypotonia benign congenital", "Benign congenital hypotonia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign congenital hypotonia", "shortest_name_length": 18}
{"curie": "MONDO:0001181", "names": ["secondary corneal edema", "Secondary corneal edema", "Secondary corneal oedema", "Secondary corneal edema (disorder)", "secondary corneal edema (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary corneal edema", "shortest_name_length": 23}
{"curie": "UMLS:C4725866", "names": ["Resectable Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Sarcoma", "shortest_name_length": 18}
{"curie": "UMLS:C0393683", "names": ["Supplementary Motor Epilepsy", "Supplementary motor epilepsy", "Epilepsy, Supplementary Motor", "Supplementary Motor Epilepsies", "Epilepsies, Supplementary Motor", "Supplementary motor epilepsy (disorder)", "Supplementary motor epilepsy (diagnosis)", "frontal lobe epilepsy supplementary motor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epilepsy, Supplementary Motor", "shortest_name_length": 28}
{"curie": "MONDO:0003142", "names": ["Embryonal Tumor", "intracranial PNET", "Intracranial PNET", "Intracranial Embryonal Tumor, NOS", "brain primitive neuroectodermal tumor", "primitive neuroectodermal tumor of brain", "intracranial primitive neuroectodermal tumor", "Intracranial Primitive Neuroectodermal Tumor", "intracranial primitive neuroectodermal neoplasm", "Intracranial Primitive Neuroectodermal Neoplasm", "Intracranial Embryonal Tumor, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intracranial primitive neuroectodermal tumor", "shortest_name_length": 15}
{"curie": "MONDO:0001001", "names": ["baritosis", "barytosis", "BARITOSIS", "Baritosis", "Barytosis", "Barium lung", "Barium lung disease", "Baritosis (disorder)", "inhalation of barytes", "baritosis (diagnosis)", "Barium pneumoconiosis", "Inhalation of barytes", "Baryta miners' disease", "Deposition of barium in the lungs", "deposition of barium in the lungs"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "baritosis", "shortest_name_length": 9}
{"curie": "UMLS:C4727143", "names": ["Metastatic Unresectable Malignant Tumor", "Metastatic Unresectable Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Unresectable Malignant Neoplasm", "shortest_name_length": 39}
{"curie": "MONDO:0026733", "names": ["MRXSHD", "MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS, 2", "Mental Retardation, X-Linked, With Marfanoid Habitus, 2", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, HACKMANN-DI DONATO TYPE", "intellectual developmental disorder, X-linked, syndromic, Hackmann-Di Donato type", "intellectual developmental disorder, X-linked, syndromic, Hackman-Di Donato type, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder, X-linked, syndromic, Hackmann-Di Donato type", "shortest_name_length": 6}
{"curie": "UMLS:C4331331", "names": ["Stage III Unknown Primary Tumor (Except for EBV-Related and HPV-Related Tumors) and Metastatic Cervical Adenopathy AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Unknown Primary Tumor (Except for EBV-Related and HPV-Related Tumors) and Metastatic Cervical Adenopathy AJCC v8", "shortest_name_length": 122}
{"curie": "MONDO:0006357", "names": ["Parotid Carcinoma ex Pleomorphic Adenoma", "parotid carcinoma ex pleomorphic adenoma", "Carcinoma ex Pleomorphic Adenoma of Parotid", "carcinoma ex pleomorphic adenoma of parotid", "Parotid Gland Carcinoma ex Pleomorphic Adenoma", "parotid gland carcinoma ex pleomorphic adenoma", "Carcinoma ex Pleomorphic Adenoma of the Parotid", "carcinoma ex pleomorphic adenoma of the parotid", "carcinoma ex pleomorphic adenoma of parotid gland", "Carcinoma ex Pleomorphic Adenoma of Parotid Gland", "Carcinoma ex pleomorphic adenoma of parotid gland", "carcinoma ex pleomorphic adenoma of the parotid gland", "Carcinoma ex Pleomorphic Adenoma of the Parotid Gland", "malignant parotid neoplasm carcinoma ex pleomorphic adenoma", "Carcinoma ex pleomorphic adenoma of parotid gland (disorder)", "Carcinoma ex pleomorphic adenoma of parotid gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parotid gland carcinoma ex pleomorphic adenoma", "shortest_name_length": 40}
{"curie": "UMLS:C1393305", "names": ["Complication;prostheses", "Prosthetic Complication", "complications; prosthetic", "complication with prostheses"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prosthetic Complication", "shortest_name_length": 23}
{"curie": "MONDO:0015092", "names": ["cleft hard palate", "Cleft hard palate", "Cleft bony palate", "cleft; palate, hard", "Cleft of hard palate", "Cleft of hard palate (disorder)", "Cleft of hard palate (diagnosis)", "cleft hard palate (physical finding)", "congenital malformation cleft of hard palate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleft hard palate", "shortest_name_length": 17}
{"curie": "UMLS:C0000814", "names": ["abortion miss", "miss abortion", "Abortion missed", "missed abortion", "abortion missed", "Missed Abortion", "ABORTION MISSED", "Missed abortion", "Missed;abortion", "ABORTION, MISSED", "Missed Abortions", "missed abortions", "Abortion, missed", "Abortion, Missed", "missed; abortion", "abortion; missed", "Abortions, Missed", "Missed miscarriage", "Silent miscarriage", "missed miscarriage", "MA - Missed abortion", "missed abortion (history)", "missed abortion; abortion", "abortion; missed abortion", "Missed abortion (disorder)", "missed abortion (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Missed abortion", "shortest_name_length": 13}
{"curie": "MONDO:0009907", "names": ["PRERETINAL VASCULAR LOOPS", "preretinal vascular loops", "Preretinal Vascular Loops", "Prepapillary vascular loop", "Prepapillary Vascular Loops", "PREPAPILLARY VASCULAR LOOPS", "Prepapillary vascular loops", "Prepapillary vascular loop (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prepapillary vascular loops", "shortest_name_length": 25}
{"curie": "MONDO:0016567", "names": ["PSEUDOCOMA", "pseudocoma", "Locked-in state", "locked-in state", "locked syndrome", "lock in syndrome", "locking syndrome", "LOCKED-IN SYNDROME", "Locked-in syndrome", "Locked-In Syndrome", "Locked in syndrome", "locked-in syndrome", "locked in syndrome", "Locked In Syndrome", "Locked-In Syndromes", "DE-EFFERENTED STATE", "'Locked in' syndrome", "Ventral Pontine Syndrome", "Ventral Pontine Syndromes", "Locked in syndrome (disorder)", "locked-in syndrome (diagnosis)", "CEREBROMEDULLOSPINAL DISCONNECTION", "Cerebromedullospinal Disconnection", "Cerebromedullospinal disconnection", "Cerebromedullospinal Disconnections", "Cerebromedullary disconnection syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "locked-in syndrome", "shortest_name_length": 10}
{"curie": "MONDO:0016462", "names": ["Isolated agammaglobulinemia", "isolated agammaglobulinemia", "agammaglobulinemia isolated", "Isolated agammaglobulinaemia", "isolated hypogammaglobulinemia", "Isolated hypogammaglobulinemia", "nonsyndromic agammaglobulinemia", "Isolated agammaglobulinemia (disorder)", "Isolated agammaglobulinemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated agammaglobulinemia", "shortest_name_length": 27}
{"curie": "UMLS:C4553238", "names": ["Stage II Penile Cancer", "Stage II Penile Cancer AJCC v8", "Stage II Penile Squamous Cell Carcinoma AJCC v8", "Stage II Squamous Cell Carcinoma of the Penis AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Penile Cancer AJCC v8", "shortest_name_length": 22}
{"curie": "MONDO:0016112", "names": ["inclusion myopathy", "cytoplasmic body myopathy", "hereditary inclusion-body myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary inclusion-body myopathy", "shortest_name_length": 18}
{"curie": "UMLS:C2347760", "names": ["Grade I Meningioma", "childhood grade I meningioma", "grade I childhood meningioma", "Childhood Grade I Meningioma", "Childhood Grade 1 Meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Grade I Meningioma", "shortest_name_length": 18}
{"curie": "UMLS:C5420825", "names": ["Refractory Acute Myelomonocytic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Acute Myelomonocytic Leukemia", "shortest_name_length": 40}
{"curie": "UMLS:C1332469", "names": ["Benign Adult Cerebral Tumor", "Benign Adult Tumor of Cerebrum", "Benign Adult Cerebral Neoplasm", "Adult Benign Cerebral Neoplasms", "Benign Adult Neoplasm of Cerebrum", "Benign Adult Tumor of the Cerebrum", "Benign Adult Neoplasm of the Cerebrum", "Benign Adult Cerebral Hemispheric Tumor", "Benign Adult Tumor of Cerebral Hemispheres", "Benign Adult Cerebral Hemispheric Neoplasm", "Benign Adult Neoplasm of Cerebral Hemispheres", "Benign Adult Tumor of the Cerebral Hemispheres", "Benign Adult Neoplasm of the Cerebral Hemispheres"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Adult Cerebral Neoplasm", "shortest_name_length": 27}
{"curie": "UMLS:C5421369", "names": ["Eye Melanocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eye Melanocytoma", "shortest_name_length": 16}
{"curie": "MONDO:0012165", "names": ["BNAR", "BNAR syndrome", "Bifid nose, anorectal anomaly, renal anomaly syndrome", "bifid nose with or without anorectal and renal anomalies", "Bifid Nose With Or Without Anorectal And Renal Anomalies", "bifid NOSE with or without anorectal and renal anomalies", "BIFID NOSE WITH OR WITHOUT ANORECTAL AND RENAL ANOMALIES", "Bifid nose with or without anorectal and renal anomalies", "BNAR (bifid nose, anorectal anomaly, renal anomaly) syndrome", "Bifid nose, anorectal anomaly, renal anomaly syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "BNAR syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0044618", "names": ["CLCN4-related X-linked intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CLCN4-related X-linked intellectual disability syndrome", "shortest_name_length": 55}
{"curie": "MONDO:0009001", "names": ["COLOBOMA OF MACULA AND SKELETAL ANOMALIES", "Coloboma of Macula and Skeletal Anomalies", "coloboma of macula and skeletal anomalies", "Macular coloboma-cleft palate-hallux valgus syndrome", "macular coloboma-cleft palate-hallux valgus syndrome", "Macular coloboma, cleft palate, hallux valgus syndrome", "Macular coloboma, cleft palate, hallux valgus syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macular coloboma-cleft palate-hallux valgus syndrome", "shortest_name_length": 41}
{"curie": "UMLS:C2981926", "names": ["Stage III Skin Melanoma AJCC v7", "Stage III Cutaneous (Skin) Melanoma", "Stage III Cutaneous Melanoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Cutaneous Melanoma AJCC v7", "shortest_name_length": 31}
{"curie": "UMLS:C4526604", "names": ["Thymoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thymoma by AJCC v8 Stage", "shortest_name_length": 24}
{"curie": "MONDO:0003341", "names": ["subungual glomus", "glomus tumor of nail", "subungual glomus tumor", "Subungual glomus tumor", "Subungual Glomus Tumor", "subungual glomus tumour", "Subungual glomus tumour", "subungual glomus (diagnosis)", "Subungual glomus tumor (disorder)", "glomus tumor of nail (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subungual glomus tumor", "shortest_name_length": 16}
{"curie": "MONDO:0024381", "names": ["jetlag", "Jetlag", "Jet Lag", "Jet lag", "jet lag", "Lag, Jet", "Jet Lags", "Lags, Jet", "jet lag syndrome", "Jet lag syndrome", "Jet Lag Syndrome", "Jet lag (finding)", "Jet Lag Syndromes", "Time zone syndrome", "Time Zone Syndrome", "Time Zone Syndromes", "time zone change syndrome", "Time Zone Change Syndrome", "Jet Lag Type Circadian Rhythm Sleep Disorder", "circadian rhythm sleep disorder, jet lag type", "sleep disorder circadian rhythm, jet lag type", "Circadian rhythm sleep disorder, jet lag type", "organic circadian rhythm sleep disorder jet lag type", "organic circadian rhythm sleep disorder, jet lag type", "nonorganic circadian rhythm sleep disorder, jet lag type", "Circadian rhythm sleep disorder, jet lag type (diagnosis)", "organic circadian rhythm sleep disorder, jet lag type (diagnosis)", "nonorganic circadian rhythm sleep disorder, jet lag type (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "circadian rhythm sleep disorder, jet lag type", "shortest_name_length": 6}
{"curie": "UMLS:C0581385", "names": ["calcified lymph node", "Calcified lymph nodes", "calcified lymph nodes", "lymph node calcification", "Lymph node calcification", "calcification lymph node", "lymph node; calcification", "calcification lymph nodes", "calcification; lymph node", "calcifications lymph nodes", "Calcified lymph nodes (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Calcified lymph nodes", "shortest_name_length": 20}
{"curie": "MONDO:0014637", "names": ["IMD40", "DOCK2 Deficiency", "DOCK2 deficiency", "immunodeficiency 40", "Immunodeficiency 40", "IMMUNODEFICIENCY 40", "immunodeficiency type 40", "DOCK2-Associated Immunodeficiency", "Dedicator of cytokinesis 2 deficiency", "Dedicator of cytokinesis 2 deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DOCK2 deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0013257", "names": ["LPRS6", "LEPROSY, SUSCEPTIBILITY TO, 6", "leprosy, susceptibility to, 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leprosy, susceptibility to, 6", "shortest_name_length": 5}
{"curie": "MONDO:0003454", "names": ["conjunctiva cancer", "Conjunctival tumor", "conjunctival tumor", "conjunctival cancer", "cancer of conjunctiva", "neoplasm of conjunctiva", "Eye cancer, conjunctival", "Malignant Conjunctiva Tumor", "malignant conjunctiva tumor", "malignant Conjunctival tumor", "malignant conjunctival tumor", "Malignant Conjunctival Tumor", "Ocular spindle cell carcinoma", "Malignant Tumor of Conjunctiva", "Malignant Conjunctiva Neoplasm", "Malignant tumor of conjunctiva", "malignant conjunctiva neoplasm", "malignant tumor of conjunctiva", "malignant conjunctival neoplasm", "Malignant Conjunctival Neoplasm", "Malignant tumour of conjunctiva", "Malignant neoplasm of conjunctiva", "Malignant Neoplasm of Conjunctiva", "malignant neoplasm of conjunctiva", "malignant tumor of the conjunctiva", "Malignant Tumor of the Conjunctiva", "malignant neoplasm of the conjunctiva", "Malignant Neoplasm of the Conjunctiva", "Malignant tumor of conjunctiva (disorder)", "malignant neoplasm of conjunctiva (primary)", "malignant neoplasm of conjunctiva (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "conjunctival cancer", "shortest_name_length": 18}
{"curie": "MONDO:0001639", "names": ["Deficiency anemia", "deficiency anemia", "anemia deficiency", "Deficiency Anemia", "deficiency anaemia", "anemia; deficiency", "deficiency anemias", "deficiency; anemia", "Deficiency anaemia", "Deficiency anemias", "anemia deficiencies", "Anemia deficiencies", "Deficiency anaemias", "Anaemia deficiencies", "ANEMIA DEFICIENCY NOS", "Deficiency anemia NOS", "Deficiency anaemia NOS", "Deficiency anemias (disorder)", "Unspecified deficiency anemia", "unspecified deficiency anemia", "Unspecified deficiency anaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deficiency anemia", "shortest_name_length": 17}
{"curie": "UMLS:C0347180", "names": ["PeIN", "Penile intraepithelial neoplasia", "penile intraepithelial neoplasia", "Penile Intraepithelial Neoplasia", "PIN - Penile intraepithelial neoplasia", "Penile intraepithelial neoplasia (disorder)", "penile intraepithelial neoplasia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Penile intraepithelial neoplasia", "shortest_name_length": 4}
{"curie": "UMLS:C4553416", "names": ["IIB", "Stage IIB Prostate Cancer", "Stage IIB Prostate Cancer AJCC v8", "Stage IIB Prostate Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Prostate Cancer AJCC v8", "shortest_name_length": 3}
{"curie": "MONDO:0008298", "names": ["oligodactyly tetramelic postaxial", "postaxial tetramelic oligodactyly", "Postaxial tetramelic oligodactyly", "postaxial oligodactyly, tetramelic", "POSTAXIAL OLIGODACTYLY, TETRAMELIC", "Postaxial Oligodactyly, Tetramelic", "Postaxial tetramelic oligodactyly (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postaxial tetramelic oligodactyly", "shortest_name_length": 33}
{"curie": "UMLS:C4288046", "names": ["Uterine Corpus Tumor Resembling Ovarian Sex Cord Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Corpus Tumor Resembling Ovarian Sex Cord Tumor", "shortest_name_length": 54}
{"curie": "MONDO:0009254", "names": ["FUCOSIDOSIS", "Fucosidosis", "fucosidosis", "Fucosidosis, NOS", "Fucosidase Deficiency", "Fucosidase deficiency", "Fucosidosis (disorder)", "A-fucosidase deficiency", "fucosidosis (diagnosis)", "mucopolysaccharidosis F", "Alpha-fucosidase deficiency", "Alpha-Fucosidase Deficiency", "alpha fucosidase deficiency", "Alpha-L-fucosidase deficiency", "Fucosidase Deficiency Disease", "ALPHA-L-FUCOSIDASE DEFICIENCY", "alpha-L-Fucosidase Deficiency", "alpha-L-fucosidase deficiency", "Deficiency Disease, Fucosidase", "Disease, Fucosidase Deficiency", "Fucosidase Deficiency Diseases", "Deficiency Diseases, Fucosidase", "Diseases, Fucosidase Deficiency", "alpha Fucosidase Deficiency Disease", "alpha-Fucosidase Deficiency Disease", "Disease, alpha-Fucosidase Deficiency", "Deficiency Disease, alpha-Fucosidase", "alpha-L-fucosidase (FUCA) deficiency", "Deficiency Disease, alpha Fucosidase", "alpha-Fucosidase Deficiency Diseases", "Deficiency Diseases, alpha-Fucosidase", "Diseases, alpha-Fucosidase Deficiency", "alpha L Fucosidase Deficiency Disease", "alpha-L-Fucosidase Deficiency Disease", "Deficiency Disease, alpha L Fucosidase", "Deficiency Disease, alpha-L-Fucosidase", "alpha-L-Fucosidase Deficiency Diseases", "Disease, alpha-L-Fucosidase Deficiency", "Diseases, alpha-L-Fucosidase Deficiency", "Deficiency Diseases, alpha-L-Fucosidase", "lysosomal storage disease caused by defective alpha-L-fucosidase with accumulation of fucose in the tissues"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fucosidosis", "shortest_name_length": 11}
{"curie": "MONDO:0009186", "names": ["EPILEPSY, PHOTOGENIC, WITH SPASTIC DIPLEGIA AND MENTAL RETARDATION", "epilepsy, photogenic, with spastic diplegia and mental retardation", "Epilepsy, Photogenic, with Spastic Diplegia and Mental Retardation", "epilepsy, photogenic, with spastic diplegia and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, photogenic, with spastic diplegia and intellectual disability", "shortest_name_length": 66}
{"curie": "MONDO:0033954", "names": ["MMAS", "Monoclonal MCAD", "Monoclonal mast cell activation syndrome", "Monoclonal Mast Cell Activation Syndrome", "monoclonal mast cell activation syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "monoclonal mast cell activation syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0242354", "names": ["birth disorder", "disorder birth", "DISORDER BIRTH", "birth disorders", "Congenital disease", "congenital disease", "disease congenital", "Congenital disorder", "congenital disorder", "congenital diseases", "Congenital Disorder", "CONGENITAL DISEASES", "congenital disorders", "Congenital Disorders", "BIRTH DISORDER (NOS)", "Disorder, Congenital", "Disorders, Congenital", "Congenital disease, NOS", "Congenital disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Disorders", "shortest_name_length": 14}
{"curie": "UMLS:C0685638", "names": ["Thoracoceloschisis", "thoracogastroschisis", "Thoracogastroschisis", "THORACOGASTROSCHISIS", "Thoracoceloschisis (disorder)", "Congenital thoracogastroschisis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thoracoceloschisis", "shortest_name_length": 18}
{"curie": "UMLS:C0862195", "names": ["Mycosis Fungoides (Working Formulation)", "Mycosis fungoides (Working Formulation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mycosis fungoides (Working Formulation)", "shortest_name_length": 39}
{"curie": "MONDO:0013823", "names": ["DFNA4B", "autosomal dominant deafness 4B", "deafness, autosomal dominant 4B", "deafness, autosomal dominant 4b", "DEAFNESS, AUTOSOMAL DOMINANT 4B", "deafness, autosomal dominant type 4B", "autosomal dominant nonsyndromic deafness 4B", "autosomal dominant nonsyndromic hearing loss 4B", "autosomal dominant nonsyndromic deafness type 4B", "CEACAM16 autosomal dominant nonsyndromic deafness", "autosomal dominant nonsyndromic deafness caused by mutation in CEACAM16"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 4B", "shortest_name_length": 6}
{"curie": "UMLS:C0278675", "names": ["Renal cancer stage I", "Hypernephroma stage I", "stage I hypernephroma", "Kidney cancer stage I", "stage I kidney cancer", "kidney cancer, stage I", "hypernephroma, stage I", "Renal carcinoma stage I", "Carcinoma kidney stage I", "Kidney carcinoma stage I", "Stage I Renal Cell Cancer", "Renal Cell Cancer Stage I", "stage I renal cell cancer", "renal cell cancer, stage I", "stage I renal cell carcinoma", "Renal cell carcinoma stage I", "Stage I Renal Cell Carcinoma", "renal cell carcinoma, stage I", "Renal Cell Carcinoma, Stage I", "Stage I Renal Cell Cancer AJCC v6", "Stage I Renal Cell Cancer AJCC v7", "Stage I Renal Cell Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Renal Cell Carcinoma", "shortest_name_length": 20}
{"curie": "UMLS:C4331224", "names": ["Recurrent T Acute Lymphoblastic Leukemia", "Recurrent Childhood T Acute Lymphoblastic Leukemia", "Recurrent Childhood T-Acute Lymphoblastic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood T Acute Lymphoblastic Leukemia", "shortest_name_length": 40}
{"curie": "MONDO:0008917", "names": ["Heart defects limb shortening", "heart defects and limb shortening", "Cardioskeletal syndrome Kuwaiti type", "cardioskeletal syndrome kuwaiti type", "CARDIOSKELETAL SYNDROME, KUWAITI TYPE", "cardioskeletal syndrome, KUWAITI type", "Cardioskeletal syndrome, Kuwaiti type", "heart defects-limb shortening syndrome", "Heart defects-limb shortening syndrome", "Heart defect and limb shortening syndrome", "heart defect and limb shortening syndrome", "Congenital heart disease and skeletal malformations", "Heart defect and limb shortening syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heart defects-limb shortening syndrome", "shortest_name_length": 29}
{"curie": "MONDO:0015765", "names": ["congenital myopathy with cores"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myopathy with cores", "shortest_name_length": 30}
{"curie": "UMLS:C0948204", "names": ["Citrobacter infection", "Infection caused by Citrobacter", "Infection caused by Citrobacter (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infection caused by Citrobacter", "shortest_name_length": 21}
{"curie": "UMLS:C1720922", "names": ["Respiratory Aspiration", "Aspiration, Respiratory"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Respiratory Aspiration", "shortest_name_length": 22}
{"curie": "MONDO:0006329", "names": ["Asthesioneuroblastoma", "esthesioneuroblastoma", "Esthesioneuroblastoma", "olfactory neuroblastoma", "Olfactory Neuroblastoma", "Olfactory neuroblastoma", "Esthesioneuroepithelioma", "Olfactory Neuroepithelioma", "Olfactory neuroepithelioma", "olfactory neuroepithelioma", "Olfactory Esthesioneuroblastoma", "olfactory esthesioneuroblastoma", "paranasal sinus olfactory neuroblastoma", "paranasal sinus Olfactory neuroblastoma", "esthesioneuroblastoma (morphologic abnormality)", "Asthesioneuroblastoma (morphologic abnormality)", "Esthesioneuroepithelioma (morphologic abnormality)", "Esthesioneuroepithelioma [dup] (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "olfactory neuroblastoma", "shortest_name_length": 21}
{"curie": "MONDO:0011338", "names": ["HMR", "Omenn Syndrome", "Omenn syndrome", "OMENN SYNDROME", "Syndrome, Omenn", "Omenns Syndrome", "Omenn's Syndrome", "Omenn's syndrome", "Syndrome, Omenn's", "Familial Reticuloendothelioses", "Familial Reticuloendotheliosis", "Reticuloendotheliosis, Familial", "Reticuloendothelioses, Familial", "HISTIOCYTIC MEDULLARY RETICULOSIS", "Histiocytic medullary reticulosis", "histiocytic medullary reticulosis", "histiocytic medullary; reticulosis", "RETICULOSIS, HISTIOCYTIC MEDULLARY", "reticulosis; histiocytic medullary", "[M]Histiocytic medullary reticulosis", "Histiocytic medullary reticulosis (disorder)", "histiocytic medullary reticulosis (diagnosis)", "combined immunodeficiency with hypereosinophilia", "Combined immunodeficiency with hypereosinophilia", "reticuloendotheliosis familial with eosinophilia", "Reticuloendotheliosis, familial, with eosinophilia", "reticuloendotheliosis, familial, with eosinophilia", "RETICULOENDOTHELIOSIS, FAMILIAL, WITH EOSINOPHILIA", "SEVERE COMBINED IMMUNODEFICIENCY WITH HYPEREOSINOPHILIA", "Severe combined immunodeficiency with hypereosinophilia", "severe combined immunodeficiency with hypereosinophilia", "Severe combined immunodeficiency with hypereosinophilia (disorder)", "severe combined immunodeficiency with hypereosinophilia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Omenn syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C1708539", "names": ["Intermediate (Rarely Metastasizing) Blood Vessel Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intermediate (Rarely Metastasizing) Blood Vessel Neoplasm", "shortest_name_length": 57}
{"curie": "MONDO:0024746", "names": ["hrade 2 Teratoma", "Grade 2 Teratoma", "Immature Teratoma", "immature teratoma", "Immature teratoma", "Teratoma, Immature", "malignant teratoma", "Embryonal teratoma", "teratoma malignant", "Malignant Teratoma", "embryonal teratoma", "Immature Teratomas", "Malignant teratoma", "Teratoma, Malignant", "Teratomas, Immature", "Teratoma, malignant", "Malignant Teratomas", "Teratomas, Malignant", "Immature teratoma, NOS", "Teratoma, malignant NOS", "Malignant teratoblastoma", "Teratoma, malignant, NOS", "Teratoblastoma, malignant", "Malignant immature teratoma", "[M]Teratoma, malignant, NOS", "Immature teratoma, malignant", "Malignant teratoma (disorder)", "malignant teratoma (diagnosis)", "Malignant teratoma (morphologic abnormality)", "Malignant immature teratoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immature teratoma", "shortest_name_length": 16}
{"curie": "MONDO:0029145", "names": ["OFC8", "orofacial cleft 8", "Orofacial Cleft 8", "OROFACIAL CLEFT 8", "Cleft Lip with or without Cleft Palate, Nonsyndromic, 8", "CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 8", "Cleft 51P With or Without Cleft Palate, Nonsyndromic, 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orofacial cleft 8", "shortest_name_length": 4}
{"curie": "MONDO:0017183", "names": ["hyperinsulinism due to UCP2 deficiency", "Hyperinsulinism due to UCP2 deficiency", "hyperinsulinemic hypoglycemia due to UCP2 deficiency", "Hyperinsulinemic hypoglycemia due to UCP2 deficiency", "Hyperinsulinism due to uncoupling protein 2 deficiency", "Hyperinsulinism due to UCP2 (uncoupling protein 2) deficiency", "Hyperinsulinism due to uncoupling protein 2 deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperinsulinism due to UCP2 deficiency", "shortest_name_length": 38}
{"curie": "MONDO:0019783", "names": ["Rubeotic glaucoma", "neovascular glaucoma", "glaucoma neovascular", "Neovascular Glaucoma", "Neovascular glaucoma", "Glaucoma, Neovascular", "Neovascular Glaucomas", "Glaucomas, Neovascular", "Neovascular glaucoma (disorder)", "Neovascular glaucoma (diagnosis)", "glaucoma secondary angle-closure, neovascular", "Secondary angle closure glaucoma with rubeosis", "secondary angle-closure glaucoma with rubeosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neovascular glaucoma", "shortest_name_length": 17}
{"curie": "UMLS:C0280152", "names": ["Stage II Lymphoblastic Lymphoma", "Adult Stage II Lymphoblastic Lymphoma", "stage II adult lymphoblastic lymphoma", "Adult Lymphoblastic Lymphoma Stage II", "Stage II Adult Lymphoblastic Lymphoma", "adult lymphoblastic lymphoma, stage II", "Stage II Adult Precursor Lymphoblastic Lymphoma", "Ann Arbor Stage II Adult Lymphoblastic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Adult Lymphoblastic Lymphoma", "shortest_name_length": 31}
{"curie": "MONDO:0038268", "names": ["autoimmune neurological channelopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune neurological channelopathy", "shortest_name_length": 37}
{"curie": "MONDO:0021490", "names": ["benign sebaceous tumor", "Benign Sebaceous Tumor", "Benign Sebaceous Neoplasm", "benign sebaceous neoplasm", "Benign Sebaceous Skin Tumor", "benign sebaceous skin tumor", "benign sebaceous gland tumor", "Benign Sebaceous Gland Tumor", "benign sebaceous skin neoplasm", "Benign Sebaceous Skin Neoplasm", "benign tumor of sebaceous gland", "sebaceous gland benign neoplasm", "Benign Sebaceous Gland Neoplasm", "benign sebaceous gland neoplasm", "Benign Tumor of Sebaceous Gland", "Benign Neoplasm of Sebaceous Gland", "Benign neoplasm of sebaceous gland", "benign neoplasm of sebaceous gland", "benign tumor of the sebaceous gland", "benign neoplasm of sebaceous glands", "Benign Tumor of the Sebaceous Gland", "Benign Neoplasm of the Sebaceous Gland", "benign neoplasm of the sebaceous gland", "Benign neoplasm of sebaceous gland (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of sebaceous gland", "shortest_name_length": 22}
{"curie": "MONDO:0011482", "names": ["CMD1I", "dilated cardiomyopathy 1I", "Cardiomyopathy, Dilated, 1i", "cardiomyopathy, dilated, 1I", "CARDIOMYOPATHY, DILATED, 1I", "dilated cardiomyopathy type 1I", "cardiomyopathy, dilated, type 1I", "DES familial isolated dilated cardiomyopathy", "familial isolated dilated cardiomyopathy caused by mutation in DES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1I", "shortest_name_length": 5}
{"curie": "UMLS:C1707674", "names": ["Densely Granulated Lactotroph PitNET/Adenoma", "Densely Granulated Pituitary Gland Lactotroph Adenoma", "Densely Granulated Lactotroph Pituitary Neuroendocrine Tumor", "Densely Granulated Lactotroph Pituitary Neuroendocrine Tumor/Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Densely Granulated Lactotroph Pituitary Neuroendocrine Tumor", "shortest_name_length": 44}
{"curie": "MONDO:0032942", "names": ["NSDVS1", "NEDMIDF", "nabais sa-de vries syndrome, type 1", "NABAIS SA-DE VRIES SYNDROME, TYPE 1", "NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY AND DYSMORPHIC FACIES", "neurodevelopmental disorder with microcephaly and dysmorphic facies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with microcephaly and dysmorphic facies", "shortest_name_length": 6}
{"curie": "MONDO:0013017", "names": ["HYPT5", "hypt5", "Muhh2", "MUHH2", "Hypt5", "HYPOTRICHOSIS 5", "Hypotrichosis 5", "hypotrichosis 5", "hypotrichosis type 5", "Marie Unna hereditary hypotrichosis 2", "Marie Unna Hereditary Hypotrichosis 2", "MARIE UNNA HEREDITARY HYPOTRICHOSIS 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotrichosis 5", "shortest_name_length": 5}
{"curie": "MONDO:0008989", "names": ["Citrulline transport defect", "citrulline transport defect", "CITRULLINE TRANSPORT DEFECT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "citrulline transport defect", "shortest_name_length": 27}
{"curie": "MONDO:0009166", "names": ["PCH4", "Young McKeever Squier syndrome", "Olivopontocerebellar hypoplasia", "olivopontocerebellar hypoplasia", "Pontocerebellar hypoplasia type 4", "Pontocerebellar Hypoplasia Type 4", "pontocerebellar hypoplasia type 4", "pontocerebellar hypoplasia, type 4", "PONTOCEREBELLAR HYPOPLASIA, TYPE 4", "PCH4 - pontocerebellar hypoplasia type 4", "Olivopontocerebellar hypoplasia lethal type", "Congenital pontocerebellar hypoplasia type 4", "Congenital pontocerebellar hypoplasia type 4 (disorder)", "Fatal infantile encephalopathy with olivopontocerebellar hypoplasia", "fatal infantile encephalopathy with olivopontocerebellar hypoplasia", "encephalopathy fatal infantile with olivopontocerebellar hypoplasia", "Encephalopathy, fatal infantile, with olivopontocerebellar hypoplasia", "ENCEPHALOPATHY, FATAL INFANTILE, WITH OLIVOPONTOCEREBELLAR HYPOPLASIA", "encephalopathy, fatal infantile, with olivopontocerebellar Hypoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pontocerebellar hypoplasia type 4", "shortest_name_length": 4}
{"curie": "MONDO:0011571", "names": ["Dfna39/Dgi1 syndrome", "DGI1/DFNA39 SYNDROME", "DFNA39/DGI1 SYNDROME", "Dgi1/Dfna39 syndrome", "DFNA39-Dentinogenesis Imperfecta 1 Syndrome", "Dfna39/dentinogenesis imperfecta 1 syndrome", "DFNA39/DENTINOGENESIS IMPERFECTA 1 SYNDROME", "deafness, autosomal dominant 39, with dentinogenesis", "DEAFNESS, AUTOSOMAL DOMINANT 39, WITH DENTINOGENESIS IMPERFECTA 1", "Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1", "deafness, autosomal dominant 39, with dentinogenesis imperfecta 1", "deafness, autosomal dominant 39, with dentinogenesis imperfecta type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness, autosomal dominant 39, with dentinogenesis imperfecta 1", "shortest_name_length": 20}
{"curie": "MONDO:0018937", "names": ["MPS3", "MPSIII", "heparitinuria", "NAGLU deficiency", "naglu deficiency", "sanfilippo disease", "Sanfilippo disease", "Sanfilippo Syndrome", "sanfilippo syndrome", "SANFILIPPO SYNDROME", "Sanfilippo syndrome", "Sanfilippos Syndrome", "Sanfilippo Syndromes", "San Filippo Syndrome", "Syndrome, Sanfilippo", "Sanfilippo syndromes", "san filippo syndrome", "Sanfilippo's Syndrome", "San Filippos Syndrome", "Sanfilippo syndrome A", "Sanfilippo's syndrome", "Sanfilippo syndrome B", "Syndromes, Sanfilippo", "sanfilippo's syndrome", "Syndrome, Sanfilippo's", "San Filippo's Syndrome", "san filippo's syndrome", "Mucopolysaccharidosis 3", "Syndrome, San Filippo's", "Sanfilippo syndrome, NOS", "HS-mucopolysaccharidosis", "mucopolysaccharidosis III", "MUCOPOLYSACCHARIDOSIS III", "Mucopolysaccharidosis III", "Mucopolysaccharidosis IIIs", "Polydystrophic Oligophrenia", "polydystrophic oligophrenia", "Polydystrophic Oligophrenias", "Mucopolysaccharidosis type 3", "mucopolysaccharidosis type 3", "Oligophrenia, Polydystrophic", "OLIGOPHRENIA, POLYDYSTROPHIC", "Mucopoly-saccharidosis type 3", "Oligophrenias, Polydystrophic", "mucopolysaccharidosis type III", "Mucopolysaccharidosis Type III", "Sanfilippo syndrome (disorder)", "Mucopolysaccharidosis, MPS-III", "mucopolysaccharidosis, MPS-III", "Mucopolysaccharidosis type III", "Sanfilippo disease (A, B, C, D)", "type III; mucopolysaccharidosis", "mucopolysaccharidosis type IIIB", "mucopolysaccharidosis type IIIA", "mucopolysaccharidosis, MPS-III-B", "MPS IIIB - Sanfilippo syndrome B", "MPS IIIA - Sanfilippo syndrome A", "Sanfilippo syndrome (A, B, C, D)", "MPS IIID - Sanfilippo syndrome D", "MPS IIIC - Sanfilippo syndrome C", "heparan sulfate sulfatase deficiency", "mucopolysaccharide storage disease III", "Mucopolysaccharidosis, type III (MPS III)", "mucopolysaccharidosis type III (diagnosis)", "N-acetyl-alpha-D-glucosaminidase deficiency", "mucopolysaccharidosis (MPS) III (A, B, C, D)", "N-sulphoglucosamine sulphohydrolase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucopolysaccharidosis type 3", "shortest_name_length": 4}
{"curie": "UMLS:C0023438", "names": ["CALLA Positive Lymphoblastic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CALLA Positive Lymphoblastic Leukemia", "shortest_name_length": 37}
{"curie": "MONDO:0014490", "names": ["MCT1D", "monocarboxylate transporter 1 deficiency", "MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY", "Ketoacidosis due to monocarboxylate transporter-1 deficiency", "ketoacidosis due to monocarboxylate transporter-1 deficiency", "Ketoacidosis due to monocarboxylate transporter-1 deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ketoacidosis due to monocarboxylate transporter-1 deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C0270425", "names": ["BIPOLAR DISORDER IN REMISSION", "Bipolar disorder in remission", "bipolar disorder in remission", "Bipolar disorder, in remission", "Bipolar disorder in remission (disorder)", "bipolar disorder in remission (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bipolar disorder in remission", "shortest_name_length": 29}
{"curie": "MONDO:0043468", "names": ["acne keloid", "keloid acne", "Acne Keloid", "Acne keloid", "keloid; acne", "Keloid, Acne", "acne; keloid", "acne keloids", "Acne Keloids", "keloid, acne", "Keloidal acne", "Keloids, Acne", "keloids, acne", "keloidal acne", "Keloidal Acne", "Sycosis nuchae", "Acne, Keloidal", "keloidal Acnes", "Keloidal Acnes", "acne, keloidal", "acne Keloidalis", "Acne Keloidalis", "acne keloidalis", "Acne keloidalis", "Acne cheloidalis", "nuchal keloid acne", "Nuchal Keloid Acne", "Keloid Acne, Nuchal", "acne, nuchal keloid", "Nuchal Keloid Acnes", "Acne, Nuchal Keloid", "nuchal keloid Acnes", "keloid acne, nuchal", "Acnes, nuchal keloid", "Keloid Acnes, Nuchal", "Acnes, Nuchal Keloid", "keloid Acnes, nuchal", "keloidal folliculitis", "Keloidal Folliculitis", "Keloidal folliculitis", "Hypertrophic acne scar", "Acne keloidalis nuchae", "Folliculitis Keloidalis", "folliculitis Keloidalis", "Folliculitis keloidalis", "Hypertrophic acne scars", "Lichen Keloidalis Nuchae", "lichen Keloidalis nuchae", "Folliculitis cheloidalis", "FOLLICULITIS CHELOIDALIS", "Keloidalis Nuchae, Lichen", "Keloidalis nuchae, lichen", "nuchae, lichen Keloidalis", "Nuchae, Lichen Keloidalis", "Acne keloidalis (disorder)", "acne keloidalis (diagnosis)", "Folliculitis keloidalis nuchae", "Folliculitis Keloidalis Nuchae", "folliculitis Keloidalis nuchae", "Keloidalis nuchae, folliculitis", "nuchae, folliculitis Keloidalis", "Nuchae, Folliculitis Keloidalis", "Keloidalis Nuchae, Folliculitis", "Dermatitis papillaris capilliti", "dermatitis papillaris Capillitii", "Dermatitis Papillaris Capillitii", "Dermatitis papillaris capillitii", "Capillitii, Dermatitis Papillaris", "Dermatitis Papillaris Capillitius", "dermatitis papillaris Capillitius", "Papillaris Capillitii, Dermatitis", "dermatitis; papillaris capillitii", "papillaris capillitii; dermatitis", "papillaris Capillitii, dermatitis", "Capillitii, dermatitis papillaris", "Hypertrophic acne scar (disorder)", "Capillitius, dermatitis papillaris", "Capillitius, Dermatitis Papillaris", "Papillaris Capillitius, Dermatitis", "papillaris Capillitius, dermatitis", "Folliculitis keloidalis nuchae (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acne keloid", "shortest_name_length": 11}
{"curie": "UMLS:C4528564", "names": ["Vulvar Composite Papillary Hidradenoma and Fibroadenoma", "Vulvar Composite Hidradenoma Papilliferum and Fibroadenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Composite Hidradenoma Papilliferum and Fibroadenoma", "shortest_name_length": 55}
{"curie": "UMLS:C0278714", "names": ["stage IV Wilms tumor", "Stage IV Wilms Tumor", "stage IV Wilms' tumor", "Wilms tumor, stage IV", "stage IV Wilm's tumor", "Wilm's tumor, stage IV", "Wilms' tumor, stage IV", "metastatic Wilms tumor", "metastatic Wilm's tumor", "stage IV nephroblastoma", "metastatic Wilms' tumor", "Wilms tumor, metastatic", "nephroblastoma, stage IV", "Wilm's tumor, metastatic", "Wilms' tumor, metastatic", "metastatic nephroblastoma", "nephroblastoma, metastatic", "Stage IV Renal Wilms Tumor", "Stage IV Renal Wilms' Tumor", "Stage IV Kidney Wilms Tumor", "Stage IV Kidney Nephroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Kidney Wilms Tumor", "shortest_name_length": 20}
{"curie": "MONDO:0001155", "names": ["gastrojejunal ulcer", "Acute stomal ulcer with hemorrhage", "Acute stomal ulcer with haemorrhage", "acute gastrojejunal ulcer with hemorrhage", "Acute gastrojejunal ulcer with hemorrhage", "Gastrojejunal ulcer, acute with hemorrhage", "acute gastrojejunal ulcer with perforation", "Acute gastrojejunal ulcer with perforation", "Acute gastrojejunal ulcer with haemorrhage", "Gastrojejunal ulcer, acute with perforation", "Gastrojejunal ulcer, acute with haemorrhage", "ulcer; gastrojejunal, acute, with hemorrhage", "ulcer; gastrojejunal, acute, with perforation", "Acute gastrojejunal ulcer with hemorrhage (disorder)", "acute gastrojejunal ulcer with hemorrhage (diagnosis)", "Acute gastrojejunal ulcer with perforation (disorder)", "acute gastrojejunal ulcer with perforation (diagnosis)", "acute gastrojejunal ulcer with hemorrhage and perforation", "acute gastrojejunal ulcer with hemorrhage and obstruction", "Acute gastrojejunal ulcer with hemorrhage and perforation", "acute gastrojejunal ulcer with hemorrhage AND perforation", "acute gastrojejunal ulcer with hemorrhage AND obstruction", "Acute gastrojejunal ulcer with hemorrhage and obstruction", "acute gastrojejunal ulcer with perforation and obstruction", "Acute gastrojejunal ulcer with perforation and obstruction", "Acute gastrojejunal ulcer with perforation AND obstruction", "Acute gastrojejunal ulcer with haemorrhage and perforation", "Acute gastrojejunal ulcer with haemorrhage and obstruction", "acute gastrojejunal ulcer with perforation AND obstruction", "acute gastrojejunal ulcer with perforation, with obstruction", "acute gastrojejunal ulcer, with hemorrhage, with obstruction", "Acute gastrojejunal ulcer, with hemorrhage, with obstruction", "Acute gastrojejunal ulcer with perforation, with obstruction", "ulcer; gastrojejunal, acute, with hemorrhage, and perforation", "Acute gastrojejunal ulcer, with haemorrhage, with obstruction", "ulcer; gastrojejunal, acute, with perforation, and hemorrhage", "Chronic gastrojejunal ulcer without hemorrhage or perforation", "Gastrojejunal ulcer, chronic without hemorrhage or perforation", "Chronic gastrojejunal ulcer without haemorrhage or perforation", "Acute gastrojejunal ulcer with both hemorrhage and perforation", "Gastrojejunal ulcer, acute with both hemorrhage and perforation", "Gastrojejunal ulcer, chronic without haemorrhage or perforation", "Gastrojejunal ulcer, acute with both haemorrhage and perforation", "acute gastrojejunal ulcer without hemorrhage AND without perforation", "Acute gastrojejunal ulcer with hemorrhage and obstruction (disorder)", "Acute gastrojejunal ulcer with hemorrhage and perforation (disorder)", "acute gastrojejunal ulcer without hemorrhage and without perforation", "Acute gastrojejunal ulcer with perforation AND obstruction (disorder)", "acute gastrojejunal ulcer with hemorrhage and obstruction (diagnosis)", "acute gastrojejunal ulcer with hemorrhage and perforation (diagnosis)", "Chronic gastrojejunal ulcer without hemorrhage AND without perforation", "chronic gastrojejunal ulcer without hemorrhage AND without perforation", "acute gastrojejunal ulcer with perforation and obstruction (diagnosis)", "chronic gastrojejunal ulcer without hemorrhage and without perforation", "Chronic gastrojejunal ulcer without haemorrhage AND without perforation", "acute gastrojejunal ulcer with hemorrhage, perforation, and obstruction", "Chronic gastrojejunal ulcer without mention of hemorrhage or perforation", "Chronic gastrojejunal ulcer without mention of haemorrhage or perforation", "Acute gastrojejunal ulcer with hemorrhage and perforation, with obstruction", "acute gastrojejunal ulcer with hemorrhage and perforation, with obstruction", "Acute gastrojejunal ulcer with hemorrhage and perforation and with obstruction", "Acute gastrojejunal ulcer with haemorrhage and perforation and with obstruction", "acute gastrojejunal ulcer with hemorrhage, with perforation and with obstruction", "Acute gastrojejunal ulcer with hemorrhage, with perforation and with obstruction", "acute gastrojejunal ulcer with hemorrhage, with perforation AND with obstruction", "Acute gastrojejunal ulcer with haemorrhage, with perforation and with obstruction", "Chronic gastrojejunal ulcer without hemorrhage AND without perforation (disorder)", "chronic gastrojejunal ulcer without hemorrhage and without perforation (diagnosis)", "acute gastrojejunal ulcer with hemorrhage, perforation, and obstruction (diagnosis)", "acute gastrojejunal ulcer without hemorrhage, without perforation and without obstruction", "acute gastrojejunal ulcer without hemorrhage, without perforation AND without obstruction", "chronic gastrojejunal ulcer without hemorrhage, without perforation AND without obstruction", "chronic gastrojejunal ulcer without hemorrhage, without perforation and without obstruction", "Acute gastrojejunal ulcer with hemorrhage, with perforation and with obstruction (disorder)", "acute gastrojejunal ulcer without mention of hemorrhage or perforation, without mention of obstruction", "chronic gastrojejunal ulcer without mention of hemorrhage or perforation, without mention of obstruction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastrojejunal ulcer", "shortest_name_length": 19}
{"curie": "UMLS:C2984897", "names": ["PHEOCHROMOCYTOMA, COMPLEX, BENIGN", "Benign Adrenal Gland Composite Pheochromocytoma", "Non-Metastatic Adrenal Gland Composite Pheochromocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Metastatic Adrenal Gland Composite Pheochromocytoma", "shortest_name_length": 33}
{"curie": "MONDO:0017912", "names": ["X-linked pure spastic paraplegia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked pure spastic paraplegia", "shortest_name_length": 32}
{"curie": "UMLS:C4521622", "names": ["Stage IVB Bone Cancer", "Stage IVB Bone Cancer AJCC v8", "Stage IVB Appendicular Skeleton, Trunk, Skull, and Facial Bones Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Bone Cancer AJCC v8", "shortest_name_length": 21}
{"curie": "MONDO:0013439", "names": ["BASD3", "CBAS3", "congenital bile acid synthesis defect 3", "Oxysterol 7-alpha-hydroxylase deficiency", "Oxysterol 7-alpha hydroxylase deficiency", "oxysterol 7-alpha-hydroxylase deficiency", "BILE ACID SYNTHESIS DEFECT, CONGENITAL, 3", "Bile Acid Synthesis Defect, Congenital, 3", "bile acid synthesis defect, congenital, 3", "congenital bile acid synthesis defect type 3", "CYP7B1 congenital bile acid synthesis defect", "Congenital bile acid synthesis defect type 3", "bile acid synthesis defect, congenital, type 3", "Congenital Bile Acid Synthesis Defect Type 3 (CBAS3)", "Congenital bile acid synthesis defect type 3 (disorder)", "congenital bile acid synthesis defect caused by mutation in CYP7B1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital bile acid synthesis defect 3", "shortest_name_length": 5}
{"curie": "UMLS:C5235061", "names": ["Pancreatic Somatostatin Producing NET", "Pancreatic Somatostatin Producing Tumor", "Pancreatic Somatostatin-Producing Neuroendocrine Tumor", "Pancreatic Somatostatin Producing Neuroendocrine Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Somatostatin-Producing Neuroendocrine Tumor", "shortest_name_length": 37}
{"curie": "MONDO:0022896", "names": ["craniosynostosis contractures cleft"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniosynostosis contractures cleft", "shortest_name_length": 35}
{"curie": "UMLS:C1336025", "names": ["Solid Alveolar Rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Solid Alveolar Rhabdomyosarcoma", "shortest_name_length": 31}
{"curie": "MONDO:0033670", "names": ["DFNB116", "deafness, autosomal recessive 116", "DEAFNESS, AUTOSOMAL RECESSIVE 116", "hearing loss, autosomal recessive 116", "autosomal recessive nonsyndromic deafness 116"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal recessive 116", "shortest_name_length": 7}
{"curie": "UMLS:C4331952", "names": ["STAT5B Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "STAT5B Deficiency", "shortest_name_length": 17}
{"curie": "MONDO:0011818", "names": ["CDT", "Fcd2", "FCD2", "CDTD", "FCDT", "CDTBC", "FCD 2B", "FCD 2A", "FCORD2", "FCD type II", "CORTICAL DYSPLASIA OF TAYLOR", "cortical dysplasia of Taylor", "Cortical dysplasia of Taylor", "focal cortical dysplasia type 2", "cortical dysplasia, Taylor type", "Focal cortical dysplasia type II", "focal cortical dysplasia, type 2", "focal cortical dysplasia type II", "Focal cortical dysplasia, type 2", "focal cortical dysplasia, type 2B", "focal cortical dysplasia, type 2A", "FOCAL CORTICAL DYSPLASIA, TYPE II", "focal cortical dysplasia, type II", "Focal Cortical Dysplasia, Type II", "focal cortical dysplasia of Taylor", "Focal cortical dysplasia of Taylor", "FOCAL CORTICAL DYSPLASIA OF TAYLOR", "isolated focal cortical dysplasia type 2", "isolated focal cortical dysplasia type II", "focal cortical dysplasia, type II, somatic", "focal cortical dysplasia of Taylor, type 2B", "Focal cortical dysplasia type II (disorder)", "focal cortical dysplasia of Taylor, type 2A", "cortical dysplasia of Taylor, dysplasia only", "CORTICAL DYSPLASIA OF TAYLOR, DYSPLASIA ONLY", "Cortical Dysplasia of Taylor, Dysplasia Only", "Focal Cortical Dysplasia of Taylor, Type IIb", "CORTICAL DYSPLASIA OF TAYLOR WITH BALLOON CELLS", "Cortical Dysplasia of Taylor with Balloon Cells", "cortical dysplasia of Taylor with balloon cells", "Cortical Dysplasia of Taylor without Balloon Cells", "CORTICAL DYSPLASIA OF TAYLOR WITHOUT BALLOON CELLS", "cortical dysplasia of Taylor without balloon cells"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated focal cortical dysplasia type II", "shortest_name_length": 3}
{"curie": "MONDO:0007205", "names": ["BDMF", "DMSMFH", "DMS-MFH", "Hardcastle syndrome", "Hardcastle's syndrome", "Hardcastle's Syndrome", "bone dysplasia with medullary fibrosarcoma", "BONE DYSPLASIA WITH MEDULLARY FIBROSARCOMA", "Bone dysplasia with medullary fibrosarcoma", "MYOPATHY, LIMB-GIRDLE, WITH BONE FRAGILITY", "myopathy, limb-girdle, with bone fragility", "Bone dysplasia-medullary fibrosarcoma syndrome", "bone dysplasia-medullary fibrosarcoma syndrome", "BONE DYSPLASIA WITH MALIGNANT FIBROUS HISTIOCYTOMA", "bone dysplasia with malignant fibrous histiocytoma", "Bone dysplasia with malignant fibrous histiocytoma", "diaphyseal medullary stenosis-bone malignancy syndrome", "Diaphyseal medullary stenosis-bone malignancy syndrome", "DIAPHYSEAL MEDULLARY STENOSIS WITH MALIGNANT FIBROUS HISTIOCYTOMA", "Diaphyseal medullary stenosis with malignant fibrous histiocytoma", "diaphyseal medullary stenosis with malignant fibrous histiocytoma", "Diaphyseal Medullary Stenosis with Malignant Fibrous Histiocytoma", "diaphyseal medullary stenosis-malignant fibrous histiocytoma syndrome", "Diaphyseal medullary stenosis-malignant fibrous histiocytoma syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diaphyseal medullary stenosis-bone malignancy syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0036688", "names": ["Rhabdomyoma", "rhabdomyoma", "rhabdomyomas", "Rhabdomyomas", "Rhabdomyoma NOS", "Rhabdomyoma, NOS", "[M]Rhabdomyoma NOS", "RHABDOMYOMA, BENIGN", "rhabdomyoma, benign", "Myoma striocellulare", "Rhabdomyoma (disorder)", "Rhabdomyomatous neoplasm", "Rhabdomyomatous Neoplasm", "Rhabdomyoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rhabdomyoma", "shortest_name_length": 11}
{"curie": "MONDO:0024234", "names": ["Seckel like syndrome majoor-krakauer type", "Bird-headed dwarfism microcephaly micrognathia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Seckel like syndrome majoor-krakauer type", "shortest_name_length": 41}
{"curie": "MONDO:0009413", "names": ["CVID2", "common variable immunodeficiency 2", "IMMUNODEFICIENCY, COMMON VARIABLE, 2", "immunodeficiency, common variable, 2", "ANTIBODY DEFICIENCY DUE TO TACI DEFECT", "antibody deficiency due to TACI defect", "immunodeficiency, common variable, type 2", "hypogammaglobulinemia due to TACI deficiency", "HYPOGAMMAGLOBULINEMIA DUE TO TACI DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency, common variable, 2", "shortest_name_length": 5}
{"curie": "MONDO:0007269", "names": ["IDC", "idc", "DCM", "IDCM", "CMD1A", "CDCD1", "Congestive Cardiomyopathy", "dilated cardiomyopathy 1A", "Dilated Cardiomyopathy-1A", "cardiomyopathy, congestive", "Cardiomyopathy, Congestive", "CARDIOMYOPATHY, CONGESTIVE", "CARDIOMYOPATHY, DILATED, 1A", "Cardiomyopathy, Dilated, 1a", "cardiomyopathy, dilated, 1A", "Congestive Cardiomyopathies", "Cardiomyopathies, Congestive", "Cardiomyopathy, Dilated, LMNA", "Cardiomyopathy, Dilated, CMD1A", "dilated cardiomyopathy type 1A", "cardiomyopathy, dilated, type 1A", "idiopathic dilated cardiomyopathy", "cardiomyopathy dilated idiopathic", "CARDIOMYOPATHY DILATED IDIOPATHIC", "Idiopathic Dilated Cardiomyopathy", "Dilated Cardiomyopathy, Idiopathic", "Familial Idiopathic Cardiomyopathy", "CARDIOMYOPATHY, IDIOPATHIC DILATED", "Cardiomyopathy, Idiopathic Dilated", "cardiomyopathy, idiopathic dilated", "idiopathic dilative cardiomyopathy", "cardiomyopathy, familial idiopathic", "Cardiomyopathy, Familial Idiopathic", "Idiopathic Cardiomyopathy, Familial", "CARDIOMYOPATHY, FAMILIAL IDIOPATHIC", "Idiopathic Dilated Cardiomyopathies", "Familial Idiopathic Cardiomyopathies", "Dilated Cardiomyopathies, Idiopathic", "Cardiomyopathies, Idiopathic Dilated", "Cardiomyopathies, Familial Idiopathic", "Idiopathic Cardiomyopathies, Familial", "Primary idiopathic dilated cardiomyopathy", "Cardiomyopathy, Dilated, Autosomal Recessive", "LMNA familial isolated dilated cardiomyopathy", "dilated cardiomyopathy with conduction defect 1", "CARDIOMYOPATHY, DILATED, WITH CONDUCTION DEFECT 1", "cardiomyopathy, dilated, with conduction defect 1", "Cardiomyopathy, Dilated, with Conduction Deffect1", "Cardiomyopathy, Dilated, With Conduction Defect 1", "Primary idiopathic dilated cardiomyopathy (disorder)", "cardiomyopathy dilated with conduction defect type 1", "familial isolated dilated cardiomyopathy caused by mutation in LMNA", "familial dilated cardiomyopathy with conduction defect due to LMNA mutation", "Familial dilated cardiomyopathy with conduction defect due to LMNA mutation", "Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation", "Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1A", "shortest_name_length": 3}
{"curie": "MONDO:0008234", "names": ["MEN 2", "MEN2a", "MEN2A", "MEA 2a", "MEN II", "men 2A", "MEN 2a", "MEN 2A", "MEA II", "MEA IIa", "MEN IIa", "men type 2", "MEA, type 2", "MEN, type 2", "men type II", "MEA type II", "MEN Type 2a", "men type 2a", "MEA type 2a", "MEA Type 2a", "MEN Type II", "men type ii", "MEA Type II", "PTC SYNDROME", "PTC syndrome", "ptc syndrome", "MEN-2A Syndrome", "men-2A syndrome", "MEN 2A Syndrome", "SIPPLE SYNDROME", "Sipple Syndrome", "MEN 2A syndrome", "sipple syndrome", "Sipple syndrome", "MEN-2A Syndromes", "Sipple's syndrome", "sipple's syndrome", "MEA syndrome, type IIa", "Familial chromaffinomatosis", "Sipple's syndrome (diagnosis)", "multiple endocrine neoplasia II", "multiple endocrine neoplasia IIA", "Multiple Endocrine Neoplasia Type 2", "Multiple endocrine neoplasia, type 2", "multiple endocrine neoplasia type 2A", "Multiple Endocrine Neoplasms Type 2a", "Multiple Endocrine Neoplasia Type 2A", "multiple endocrine neoplasia type II", "MULTIPLE ENDOCRINE NEOPLASIA TYPE II", "Multiple endocrine neoplasia Type 2A", "Multiple endocrine neoplasia type 2A", "Multiple Endocrine Neoplasia Type II", "Multiple Endocrine Neoplasia Type 2a", "multiple endocrine neoplasia, type 2A", "Multiple Endocrine Neoplasia, Type II", "type IIa multiple endocrine neoplasia", "Neoplasms, Multiple Endocrine Type 2a", "Multiple endocrine neoplasia Type IIA", "thyroid carcinoma, familial medullary", "Neoplasia, Multiple Endocrine Type 2a", "multiple endocrine neoplasia, type II", "multiple endocrine neoplasia, type IIA", "Multiple Endocrine Neoplasia, Type IIa", "MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA", "Multiple endocrine adenomatosis, type 2", "multiple endocrine adenomatosis type 2a", "multiple endocrine adenomatosis type 2A", "Multiple Endocrine Adenomatosis Type II", "Multiple Endocrine Adenomatosis Type 2a", "multiple endocrine adenomatosis type II", "Multiple Endocrine Adenomatosis Type 2A", "Multiple Endocrine Adenomatosis, Type II", "Multiple endocrine adenomatosis Type IIa", "multiple endocrine adenomatosis, type II", "Multiple endocrine adenomatosis, type IIa", "MEN (multiple endocrine neoplasia) type 2A", "Multiple endocrine neoplasia [MEN] type IIA", "MEN2A - multiple endocrine neoplasia type 2A", "multiple endocrine neoplasia type 2A (MEN 2A)", "Multiple endocrine neoplasia syndrome type 2A", "Multiple endocrine neoplasia type 2A (disorder)", "type IIa multiple endocrine neoplasia (diagnosis)", "MEN 2A - Multiple endocrine neoplasia syndrome type 2A", "PHEOCHROMOCYTOMA AND AMYLOID-PRODUCING MEDULLARY THYROID CARCINOMA", "pheochromocytoma and amyloid producing medullary thyroid carcinoma", "Pheochromocytoma And Amyloid-Producing Medullary Thyroid Carcinoma", "Pheochromocytoma And Amyloid Producing Medullary Thyroid Carcinoma", "pheochromocytoma and amyloid-producing medullary thyroid carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple endocrine neoplasia type 2A", "shortest_name_length": 5}
{"curie": "UMLS:C1335020", "names": ["Non-Neoplastic Mediastinal Disease", "Non-Neoplastic Mediastinal Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Mediastinal Disorder", "shortest_name_length": 34}
{"curie": "MONDO:0007176", "names": ["AA", "SCRA", "HPCD", "Atrophia Areata", "Atrophia areata", "atrophia areata", "ATROPHIA AREATA", "Sveinsson Chorioretinal Atrophy", "SVEINSSON CHORIORETINAL ATROPHY", "SVEINSSON chorioretinal atrophy", "Sveinsson chorioretinal atrophy", "Helicoid peripapillary chorioretinal degeneration", "helicoid peripapillary chorioretinal degeneration", "HELICOIDAL PERIPAPILLARY CHORIORETINAL DEGENERATION", "helicoidal peripapillary chorioretinal Degeneration", "Helicoidal Peripapillary Chorioretinal Degeneration", "Peripapillary Chorioretinal Degeneration, Icelandic Type", "peripapillary chorioretinal degeneration, Icelandic type", "PERIPAPILLARY CHORIORETINAL DEGENERATION, ICELANDIC TYPE", "peripapillary chorioretinal Degeneration, Icelandic type", "Helicoid peripapillary chorioretinal degeneration (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "helicoid peripapillary chorioretinal degeneration", "shortest_name_length": 2}
{"curie": "UMLS:C1392046", "names": ["Cardiovascular insufficiency", "Cardiovascular Insufficiency", "cardiovascular; insufficiency", "insufficiency; cardiovascular"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiovascular insufficiency", "shortest_name_length": 28}
{"curie": "MONDO:0003943", "names": ["nervous system hibernoma", "Hibernoma of nervous system", "hibernoma of nervous system", "central nervous system hibernoma", "Central Nervous System Hibernoma", "hibernoma of central nervous system", "Hibernoma of Central Nervous System", "hibernoma of the central nervous system", "Hibernoma of the Central Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system hibernoma", "shortest_name_length": 24}
{"curie": "MONDO:0011804", "names": ["Ceds", "CEDS", "ALPS2B", "Caspase 8 deficiency", "caspase-8 deficiency", "caspase 8 deficiency", "Caspase 8 Deficiency", "Caspase-8 Deficiency", "CASPASE 8 DEFICIENCY", "Deficiency, Caspase-8", "Deficiency, Caspase 8", "Caspase 8 Deficiencies", "Caspase-8 Deficiencies", "Deficiencies, Caspase-8", "Deficiencies, Caspase 8", "Caspase 8 deficiency syndrome", "caspase 8 deficiency syndrome", "Caspase eight deficiency state", "caspase eight deficiency state", "ALPS with recurrent viral infections", "CASP8 autoimmune lymphoproliferative syndrome", "autoimmune lymphoproliferative syndrome type 2B", "Autoimmune Lymphoproliferative Syndrome Type 2B", "autoimmune lymphoproliferative syndrome type IIB", "autoimmune lymphoproliferative syndrome, type 2B", "autoimmune lymphoproliferative syndrome, type IIB", "AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIB", "Autoimmune Lymphoproliferative Syndrome, Type IIb", "Autoimmune Lymphoproliferative Syndrome Type 2B (ALPS2B)", "autoimmune lymphoproliferative syndrome caused by mutation in CASP8", "autoimmune lymphoproliferative syndrome with recurrent viral infection", "Autoimmune lymphoproliferative syndrome with recurrent viral infection", "autoimmune lymphoproliferative syndrome with recurrent viral infections", "Autoimmune lymphoproliferative syndrome with recurrent viral infections", "Autoimmune lymphoproliferative syndrome with recurrent viral infection (disorder)", "autoimmune lymphoproliferative syndrome with recurrent viral infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune lymphoproliferative syndrome type 2B", "shortest_name_length": 4}
{"curie": "MONDO:0002471", "names": ["bursitis", "Bursitis", "BURSITIS", "capsulitis", "Bursitides", "Capsulitides", "Bursitis NOS", "Bursitis, NOS", "frozen shoulder", "Bursal synovitis", "frozen shoulders", "shoulder, frozen", "shoulders, frozen", "bursa inflammation", "adhesive capsulitis", "Bursitis (disorder)", "capsulitis, adhesive", "bursitis (diagnosis)", "Inflammation of bursa", "inflammation of bursa", "adhesive Capsulitides", "Capsulitides, adhesive", "synovial bursa inflammation", "shoulder adhesive capsulitis", "capsulitis, shoulder adhesive", "adhesive capsulitis, shoulder", "shoulder adhesive Capsulitides", "inflammation of synovial bursa", "Capsulitides, shoulder adhesive", "adhesive Capsulitides, shoulder", "adhesive capsulitis of the shoulder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bursitis", "shortest_name_length": 8}
{"curie": "UMLS:C0281702", "names": ["Stage II Burkitt Lymphoma", "Stage II Childhood Burkitt Lymphoma", "Stage II Childhood Burkitt's Lymphoma", "Ann Arbor Stage II Childhood Burkitt Lymphoma", "stage II childhood small noncleaved cell lymphoma", "Stage II Childhood Small Non-Cleaved Cell Lymphoma", "childhood small noncleaved cell lymphoma, stage II", "Childhood Small Non-Cleaved Cell Lymphoma Stage II", "Pediatric Small Non-Cleaved Cell Lymphoma Stage II", "lymphoma, stage II childhood small noncleaved cell", "Stage II Pediatric Small Non-Cleaved Cell Lymphoma", "stage II small noncleaved cell lymphoma, childhood", "pediatric small noncleaved cell lymphoma, stage II", "small noncleaved cell lymphoma, childhood, stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Childhood Burkitt Lymphoma", "shortest_name_length": 25}
{"curie": "MONDO:0014813", "names": ["HLD13", "HIKESHI leukodystrophy", "hikeshi leukodystrophy", "hypomyelinating leukodystrophy 13", "leukodystrophy, hypomyelinating, 13", "LEUKODYSTROPHY, HYPOMYELINATING, 13", "hypomyelinating leukodystrophy type 13", "leukodystrophy, hypomyelinating, type 13", "leukodystrophy caused by mutation in HIKESHI", "leukodystrophy caused by mutation in hikeshi"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypomyelinating leukodystrophy 13", "shortest_name_length": 5}
{"curie": "UMLS:C1698036", "names": ["small intestine infection", "Small intestine infection", "Small Intestinal Infection", "small intestine infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Intestinal Infection", "shortest_name_length": 25}
{"curie": "MONDO:0006178", "names": ["Dedifferentiated Solitary Fibrous Tumor", "Dedifferentiated solitary fibrous tumor", "dedifferentiated solitary fibrous tumor", "Dedifferentiated solitary fibrous tumour", "Dedifferentiated solitary fibrous tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dedifferentiated solitary fibrous tumor", "shortest_name_length": 39}
{"curie": "MONDO:0017287", "names": ["IgG4-RD", "IgG4-syndrome", "hyper-IgG4 disease", "IgG4-Related Disease", "IgG4-related disease", "IgG4-associated disease", "multifocal fibrosclerosis", "IgG4-related systemic disease", "IgG4-Related Sclerosing Disease", "IgG4 Related Sclerosing Disease", "IgG4-related sclerosing disease", "IgG4-related autoimmune disease", "IgG4 related sclerosing disease", "IgG4-Related Sclerosing Diseases", "Sclerosing Disease, IgG4-Related", "multifocal idiopathic fibrosclerosis", "IgG4-related systemic sclerosing disease", "systemic IgG4-related sclerosing syndrome", "systemic IgG4-related plasmacytic syndrome", "IgG4-related sclerosing disease (diagnosis)", "Immunoglobulin G4-related sclerosing disease", "Immunoglobulin G4 Related Sclerosing Disease", "Immunoglobulin G4-Related Sclerosing Disease", "Immunoglobulin G4 related sclerosing disease", "IgG4-positive multiorgan lymphoproliferative syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IgG4-related disease", "shortest_name_length": 7}
{"curie": "MONDO:0001316", "names": ["Streptococcal meningitis", "Meningitis streptococcal", "streptococcal meningitis", "meningitis streptococcal", "meningitis; streptoccocal", "streptoccocal; meningitis", "Streptococcus infectious meningitis", "Streptococcal meningitis (disorder)", "Streptococcal meningitis (diagnosis)", "Streptococcus caused infectious meningitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "streptococcal meningitis", "shortest_name_length": 24}
{"curie": "MONDO:0005932", "names": ["Mad itch", "Pseudorabies", "pseudorabies", "Aujeszky Disease", "Aujeszkys Disease", "Aujeszky's Disease", "Aujeszky's disease", "Pseudorabies (disorder)", "Infectious bulbar paralysis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudorabies", "shortest_name_length": 8}
{"curie": "UMLS:C4524926", "names": ["Metastatic Digestive System Cancer", "Metastatic Gastrointestinal Carcinoma", "Metastatic Digestive System Carcinoma", "Metastatic Gastrointestinal System Cancer", "Metastatic Gastrointestinal System Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Digestive System Carcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0035500", "names": ["congenital primary lymphedema of Gordon", "VEGFC-related congenital primary lymphedema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital primary lymphedema of Gordon", "shortest_name_length": 39}
{"curie": "UMLS:C4682801", "names": ["Stage IB Testicular Cancer", "Stage IB Testicular Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Testicular Cancer AJCC v8", "shortest_name_length": 26}
{"curie": "MONDO:0013455", "names": ["CMH16", "hypertrophic cardiomyopathy 16", "cardiomyopathy, hypertrophic, 16", "MYOZ2 hypertrophic cardiomyopathy", "hypertrophic cardiomyopathy type 16", "cardiomyopathy familial hypertrophic 16", "CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 16", "cardiomyopathy, familial hypertrophic, 16", "cardiomyopathy, familial hypertrophic, type 16", "hypertrophic cardiomyopathy caused by mutation in MYOZ2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophic cardiomyopathy 16", "shortest_name_length": 5}
{"curie": "UMLS:C1336380", "names": ["Stage IVB Nasopharynx Keratinizing Epidermoid Carcinoma", "Stage IVB Keratinizing Epidermoid Carcinoma of Nasopharynx", "Stage IVB Nasopharyngeal Keratinizing Epidermoid Carcinoma", "Stage IVB Nasopharynx Keratinizing Squamous Cell Carcinoma", "Stage IVB Nasopharyngeal Keratinizing Squamous Cell Carcinoma", "Stage IVB Keratinizing Squamous Cell Carcinoma of Nasopharynx", "Stage IVB Keratinizing Epidermoid Carcinoma of the Nasopharynx", "Stage IVB Nasopharyngeal Throat Keratinizing Squamous Cell Cancer", "Stage IVB Keratinizing Squamous Cell Carcinoma of the Nasopharynx", "Stage IVB Nasopharyngeal Keratinizing Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Nasopharyngeal Keratinizing Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 55}
{"curie": "UMLS:C0343363", "names": ["Rotaviral Enteritis", "Rotaviral enteritis", "Rotaviral gastroenteritis", "Rotavirus gastroenteritis", "ROTAVIRUS GASTROENTERITIS", "Gastroenteritis rotavirus", "rotavirus gastroenteritis", "rotaviral; gastroenteritis", "gastroenteritis; rotaviral", "gastroenteritis due to rotavirus", "viral gastroenteritis (rotavirus)", "gastroenteritis; viral, rotaviral", "viral; gastroenteritis, rotaviral", "Viral gastroenteritis due to Rotavirus", "Viral gastroenteritis due to Rotaviruses", "Viral gastroenteritis caused by Rotavirus", "gastroenteritis due to rotavirus (diagnosis)", "Viral gastroenteritis caused by Rotavirus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Viral gastroenteritis due to Rotavirus", "shortest_name_length": 19}
{"curie": "UMLS:C0795692", "names": ["Hyperlactatemia", "Hyperlactataemia", "Hyperlactatemias", "Hyperlactacidemia", "Hyperlactacidaemia", "LACTIC ACID INCREASED", "Lactate blood increase", "LACTATE BLOOD INCREASE", "Lactate blood increased", "LACTATE BLOOD INCREASED", "Lactate Blood Increased", "Increased blood lactate", "LACTIC ACID BLOOD INCREASED", "Increased blood lactic acid", "Lactic acid blood increased", "Blood lactic acid increased"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyperlactatemia", "shortest_name_length": 15}
{"curie": "MONDO:0043765", "names": ["presbycusis", "Presbycusis", "PRESBYCUSIS", "Presbycuses", "presbyacusis", "Presbyacusis", "presbyacusia", "PRESBYACUSIS", "Presbyacusia", "Senile deafness", "senile deafness", "Presbycusis;senile", "senile presbyacusis", "Senile presbyacusis", "Presbycusis syndrome", "Presbycusis (disorder)", "Deafness due to old age", "presbycusis (diagnosis)", "age-related hearing loss", "age related hearing loss", "Age-related hearing loss", "Hearing loss, age-related", "Presbycusis, unspecified ear", "hard of hearing (presbyacusis)", "Old-aged sensorineural hearing impairment"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "presbycusis", "shortest_name_length": 11}
{"curie": "UMLS:C0855106", "names": ["Burkitt's tumor stage I", "Burkitt's tumour stage I", "Stage I Burkitt Lymphoma", "Burkitt's Lymphoma Stage I", "Stage I Burkitt's Lymphoma", "Burkitt's lymphoma stage I", "Ann Arbor Stage I Burkitt Lymphoma", "Burkitt's tumor or lymphoma stage I", "Burkitt's tumour or lymphoma stage I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Burkitt Lymphoma", "shortest_name_length": 23}
{"curie": "UMLS:C0264268", "names": ["Nasal septal ulcer", "nasal septum ulcer", "nasal septal ulcers", "ulcer of nasal septum", "Ulcer of nasal septum", "NOSE SEPTUM ULCERATION", "NASAL SEPTUM ULCERATION", "Nasal septum ulceration", "Ulcer of nasal septum (disorder)", "ulcer of nasal septum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ulcer of nasal septum", "shortest_name_length": 18}
{"curie": "MONDO:0009551", "names": ["magnesium, elevated red cell", "MAGNESIUM, ELEVATED RED CELL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "magnesium, elevated red cell", "shortest_name_length": 28}
{"curie": "MONDO:0007834", "names": ["INSDM", "nesidioblastosis", "NESIDIOBLASTOSIS", "Nesidioblastosis", "Nesidioblastoses", "Islet cell hyperplasia", "islet cell hyperplasia", "islet cell adenomatosis", "ISLET CELL ADENOMATOSIS", "Islet Cell Adenomatosis", "Islet cell adenomatosis", "Pancreas Nesidioblastoses", "Pancreas Nesidioblastosis", "Islet cell hyperplasia NOS", "Islet-cell hyperplasia NOS", "Islet cell hyperplasia, NOS", "Pancreatic Nesidioblastoses", "Pancreatic Nesidioblastosis", "Nesidioblastosis, Pancreatic", "Nesidioblastosis of Pancreas", "Nesidioblastoses, Pancreatic", "nesidioblastosis (diagnosis)", "NESIDIOBLASTOSIS OF PANCREAS", "Pancreatic B-cell adenomatosis", "Islet cell hyperplasia (disorder)", "Islet cell adenomatosis (disorder)", "Pancreatic endocrine cell hyperplasia", "INSULINOMATOSIS AND DIABETES MELLITUS", "INSULINOMATOSIS and diabetes mellitus", "Insulinomatosis and diabetes mellitus", "Hyperinsulinemia due to nesidioblastosis", "Pancreatic endocrine cell hyperplasia NOS", "Hyperinsulinaemia due to nesidioblastosis", "Persistent hyperinsulinaemic hypoglycemia of infancy", "Familial hyperinsulinemia with pancreatic nesidioblastosis", "PHHI - Persistent hyperinsulinaemic hypoglycemia of infancy", "Hyperinsulinism, Familial, with Pancreatic Nesidioblastosis", "HYPERINSULINISM, FAMILIAL, WITH PANCREATIC NESIDIOBLASTOSIS", "Familial hyperinsulinaemia with pancreatic nesidioblastosis", "Hyperinsulinemia due to pancreatic islet beta cell hyperplasia", "Hyperinsulinaemia due to pancreatic islet beta cell hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "islet cell adenomatosis", "shortest_name_length": 5}
{"curie": "OMIM:177600", "names": ["PSEUDOCHOLINESTERASE, INCREASE IN PLASMA LEVEL OF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 49}
{"curie": "MONDO:0018870", "names": ["GACI", "IIAC", "Infantile arteriosclerosis", "infantile arteriosclerosis", "occlusive infantile arteriopathy", "Occlusive infantile arteriopathy", "Arteriopathy, Occlusive Infantile", "ARTERIOPATHY, OCCLUSIVE INFANTILE", "Arterial calcification of infancy", "arterial calcification of infancy", "Idiopathic obliterative arteriopathy", "idiopathic obliterative arteriopathy", "Idiopathic infantile arterial calcification", "IDIOPATHIC INFANTILE ARTERIAL CALCIFICATION", "idiopathic infantile arterial calcification", "Arterial Calcification, Idiopathic Infantile", "ARTERIAL CALCIFICATION, IDIOPATHIC INFANTILE", "generalized arterial calcification of infancy", "Generalized arterial calcification in infancy", "Generalized arterial calcification of infancy", "generalized arterial calcification in infancy", "Arterial Calcification, Generalized, Of Infancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arterial calcification of infancy", "shortest_name_length": 4}
{"curie": "MONDO:0800127", "names": ["pulmonary amyloidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary amyloidosis", "shortest_name_length": 21}
{"curie": "UMLS:C3273217", "names": ["Invasive Breast Lobular Carcinoma, Solid Variant", "Invasive Lobular Breast Carcinoma, Solid Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Invasive Breast Lobular Carcinoma, Solid Variant", "shortest_name_length": 48}
{"curie": "UMLS:C0235097", "names": ["Withdrawal fits", "withdrawal seizure", "WITHDRAWAL SEIZURE", "Withdrawal seizures", "seizures withdrawal", "withdrawal seizures", "Withdrawal epilepsy", "WITHDRAWAL CONVULSIONS", "Withdrawal convulsions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Withdrawal convulsions", "shortest_name_length": 15}
{"curie": "MONDO:0020627", "names": ["epileptic encephalopathy, infantile or early childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epileptic encephalopathy, infantile or early childhood", "shortest_name_length": 54}
{"curie": "MONDO:0001508", "names": ["patulous eustachian tube", "Eustachian tube patulous", "Patulous eustachian tube", "Patulous Eustachian tube", "eustachian tube; patulous", "eustachian patulous tubes", "patulous; eustachian tube", "Patulous eustachian tube (disorder)", "patulous eustachian tube (diagnosis)", "Patulous Eustachian tube, unspecified ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "patulous eustachian tube", "shortest_name_length": 24}
{"curie": "MONDO:0013012", "names": ["IBD27", "INFLAMMATORY BOWEL DISEASE 27", "Inflammatory Bowel Disease 27", "inflammatory bowel disease 27", "inflammatory bowel disease type 27"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory bowel disease 27", "shortest_name_length": 5}
{"curie": "UMLS:C0333732", "names": ["Karyolysis", "karyolysis", "karyorrhexis", "Karyorrhexis", "Nuclear degeneration", "Karyorrhexis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Karyorrhexis", "shortest_name_length": 10}
{"curie": "MONDO:0100309", "names": ["SCA", "ataxia hereditary", "Hereditary Ataxia", "hereditary ataxia", "Hereditary ataxia", "hereditary; ataxia", "Ataxia, hereditary", "ataxia; hereditary", "Ataxia, Hereditary", "Hereditary Ataxias", "hereditary ataxias", "Ataxias, Hereditary", "Hereditary ataxia NOS", "rare hereditary ataxia", "Hereditary spinal ataxia", "Hereditary ataxia (disorder)", "hereditary ataxia (diagnosis)", "Hereditary ataxia, unspecified", "Familial Spinocerebellar Degeneration", "Spinocerebellar Degeneration, Familial", "Familial Spinocerebellar Degenerations", "Degeneration, Familial Spinocerebellar", "spinocerebellar; disorder (hereditary)", "Inherited Spinocerebellar Degeneration", "Spinocerebellar Degeneration, Inherited", "Degeneration, Inherited Spinocerebellar", "Inherited Spinocerebellar Degenerations", "Spinocerebellar Degenerations, Familial", "Degenerations, Familial Spinocerebellar", "Hereditary Spinocerebellar Degeneration", "Spinocerebellar Degenerations, Inherited", "Spinocerebellar Degeneration, Hereditary", "Degenerations, Inherited Spinocerebellar", "Degeneration, Hereditary Spinocerebellar", "Hereditary Spinocerebellar Degenerations", "Degenerations, Hereditary Spinocerebellar", "Spinocerebellar Degenerations, Hereditary", "disease (or disorder); spinocerebellar (hereditary)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary ataxia", "shortest_name_length": 3}
{"curie": "MONDO:0017497", "names": ["Femorotibiofibular intercalary transverse meromelia, bilateral", "congenital absence of thigh and lower leg with foot present, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital absence of thigh and lower leg with foot present, bilateral", "shortest_name_length": 62}
{"curie": "UMLS:C4013425", "names": ["Cervical Neuroendocrine Cancer", "Cervical Neuroendocrine Carcinoma", "Neuroendocrine cervical carcinoma", "Cervical High Grade Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neuroendocrine cervical carcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0002217", "names": ["CNS Sarcoma", "CNS sarcoma", "sarcoma of CNS", "Sarcoma of CNS", "Sarcoma of the CNS", "sarcoma of the CNS", "Central Nervous System Sarcoma", "central nervous system sarcoma", "Sarcoma of Central Nervous System", "sarcoma of central nervous system", "sarcoma of the central nervous system", "Sarcoma of the Central Nervous System", "sarcoma of central nervous system (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system sarcoma", "shortest_name_length": 11}
{"curie": "MONDO:0020414", "names": ["persistent fifth aortic arch"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "persistent fifth aortic arch", "shortest_name_length": 28}
{"curie": "MONDO:0011549", "names": ["HTS", "Hts", "Hhs", "HHS", "Hypt1", "HYPT1", "hypotrichosis 1", "HYPOTRICHOSIS 1", "hypotrichosis type 1", "APCDD1 hypotrichosis", "hypotrichosis caused by mutation in APCDD1", "hereditary generalized hypotrichosis simplex", "hypotrichosis simplex, generalized, hereditary", "HYPOTRICHOSIS SIMPLEX, GENERALIZED, HEREDITARY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotrichosis 1", "shortest_name_length": 3}
{"curie": "MONDO:0001574", "names": ["microangiopathy", "Microangiopathy", "capillary disease", "Capillary disease", "CAPILLARY DISORDER", "Capillary disorder", "capillary disorder", "Microangiopathy NOS", "Capillary Disorders", "capillary disorders", "Microangiopathy, NOS", "disease of capillary", "disorder of capillary", "Capillary disease, NOS", "Capillary disorder NOS", "disease of capillaries", "Disease of capillaries", "Capillary disorder, NOS", "Diseases of capillaries", "Disorder of capillaries", "Capillary vascular disease", "DISEASES OF THE CAPILLARIES", "Disease of capillaries, NOS", "capillary disease or disorder", "capillary disease (diagnosis)", "disease or disorder of capillary", "disease (or disorder); capillaries", "Disorder of capillaries (disorder)", "Disease of capillaries, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "capillary disorder", "shortest_name_length": 15}
{"curie": "UMLS:C5554635", "names": ["Locally Advanced Lung Large Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Lung Large Cell Neuroendocrine Carcinoma", "shortest_name_length": 57}
{"curie": "UMLS:C1698447", "names": ["Infusion site mass"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infusion site mass", "shortest_name_length": 18}
{"curie": "MONDO:0014758", "names": ["RUSAT2", "RADIOULNAR SYNOSTOSIS AND AMEGAKARYOCYTIC THROMBOCYTOPENIA 2", "RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 2", "radioulnar synostosis with amegakaryocytic thrombocytopenia 2", "radioulnar synostosis with amegakaryocytic thrombocytopenia type 2", "radioulnar synostosis with amegakaryocytic thrombocytopenia 2; RUSAT2", "MECOM radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome", "radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome caused by mutation in MECOM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radioulnar synostosis with amegakaryocytic thrombocytopenia 2", "shortest_name_length": 6}
{"curie": "UMLS:C2828207", "names": ["Stage IVB Bone Cancer", "Stage IVB Bone Cancer AJCC v7", "Stage IVB Bone Cancer  AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Bone Cancer AJCC v7", "shortest_name_length": 21}
{"curie": "MONDO:0017686", "names": ["aminoacylase deficiency", "inborn aminoacylase deficiency", "inborn error of aminoacylase activity", "inborn aminoacylase activity disorder", "rare inborn error of aminoacylase activity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn aminoacylase deficiency", "shortest_name_length": 23}
{"curie": "UMLS:C0220650", "names": ["Brain Metastase", "brain secondary", "BRAIN METASTASES", "metastasis brain", "Brain metastasis", "Brain Metastasis", "brain metastases", "Brain Metastases", "brain metastasis", "BRAIN METASTASIS", "Brain metastases", "Brain secondaries", "Metastasis to brain", "metastasis to brain", "Metastases to brain", "secondary brain cancer", "metastatic brain tumor", "brain metastatic tumor", "brain tumor metastatic", "brain cancer secondary", "BRAIN TUMOR METASTATIC", "brain cancer metastatic", "metastatic brain cancer", "Brain cancer metastatic", "metastasis to the brain", "brain metastatic tumors", "brain cancers metastatic", "Secondary cancer of brain", "tumors metastatic to brain", "metastatic cancer to brain", "Cancer metastatic to brain", "cancer metastatic to brain", "cancer, metastatic to brain", "Metastatic Tumor to the Brain", "metastasis to brain (diagnosis)", "Metastatic Neoplasm to the Brain", "Metast. to brain parenchyma, NOS", "secondary malignant neoplasm brain", "Metastases to brain parenchyma, NOS", "secondary malignant neoplasm of brain", "Secondary malignant neoplasm of brain", "Metastatic malignant neoplasm to brain", "Metastatic malignant neoplasm of brain", "Metastatic Malignant Neoplasm in the Brain", "Metastatic Malignant Neoplasm to the Brain", "Secondary malignant neoplasm of brain, NOS", "Metastatic malignant neoplasm to brain, NOS", "secondary malignant neoplasm of brain (diagnosis)", "Metastatic malignant neoplasm to brain (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to brain", "shortest_name_length": 15}
{"curie": "MONDO:0010126", "names": ["THYMIC APLASIA WITH FETAL DEATH", "Thymic Aplasia with Fetal Death", "thymic aplasia with fetal death"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thymic aplasia with fetal death", "shortest_name_length": 31}
{"curie": "MONDO:0009803", "names": ["Osteogenesis imperfecta congenita, microcephaly, and cataracts", "osteogenesis imperfecta congenita, microcephaly, and cataracts", "OSTEOGENESIS IMPERFECTA CONGENITA, MICROCEPHALY, AND CATARACTS", "congenital osteogenesis imperfecta-microcephaly-cataracts syndrome", "Congenital osteogenesis imperfecta-microcephaly-cataracts syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital osteogenesis imperfecta-microcephaly-cataracts syndrome", "shortest_name_length": 62}
{"curie": "MONDO:0016364", "names": ["JS-O", "JBTS3", "Joubert syndrome 3", "Joubert syndrome with retinopathy", "Joubert syndrome with ocular defect", "Joubert syndrome with ocular anomalies", "Joubert syndrome with ocular defect (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome with ocular defect", "shortest_name_length": 4}
{"curie": "MONDO:0008229", "names": ["accessory deep peroneal nerve", "Accessory deep peroneal nerve", "PERONEAL NERVE, ACCESSORY DEEP", "peroneal nerve, accessory deep", "Peroneal nerve, accessory deep"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroneal nerve, accessory deep", "shortest_name_length": 29}
{"curie": "UMLS:C5237416", "names": ["Recurrent Metastatic Merkel Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Metastatic Merkel Cell Carcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0012271", "names": ["MSSD", "syndactyly type 9", "Syndactyly type 9", "syndactyly, type 9", "SYNDACTYLY, TYPE IX", "Syndactyly, Type IX", "syndactyly Malik-Percin type", "Syndactyly Malik Percin type", "Syndactyly, Malik-Percin type", "SYNDACTYLY, MALIK-PERCIN TYPE", "syndactyly, Malik-Percin type", "Syndactyly, Malik-Percin Type", "mesoaxial synostotic syndactyly with phalangeal reduction", "Mesoaxial synostotic syndactyly with phalangeal reduction", "syndactyly mesoaxial synostotic with phalangeal reduction", "SYNDACTYLY, MESOAXIAL SYNOSTOTIC, WITH PHALANGEAL REDUCTION", "syndactyly, mesoaxial synostotic, with phalangeal reduction", "Syndactyly, Mesoaxial Synostotic, with Phalangeal Reduction", "Mesoaxial synostotic syndactyly with phalangeal reduction syndrome", "Mesoaxial synostotic syndactyly with phalangeal reduction syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mesoaxial synostotic syndactyly with phalangeal reduction", "shortest_name_length": 4}
{"curie": "MONDO:0032757", "names": ["CILD41", "primary ciliary dyskinesia 41", "CILIARY DYSKINESIA, PRIMARY, 41", "ciliary dyskinesia, primary, 41"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ciliary dyskinesia, primary, 41", "shortest_name_length": 6}
{"curie": "UMLS:C5446574", "names": ["Conjunctival Lymphangioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conjunctival Lymphangioma", "shortest_name_length": 25}
{"curie": "MONDO:0032921", "names": ["NEDHRIT", "NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, NEONATAL RESPIRATORY INSUFFICIENCY, AND THERMODYSREGULATION", "neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation", "shortest_name_length": 7}
{"curie": "UMLS:C0280150", "names": ["high-grade, stage II adult NHL", "NHL, high grade, stage II adult", "adult NHL, stage II, high grade", "Stage II High Grade Adult Non-Hodgkin's Lymphoma", "lymphoma, high grade, stage II adult non-Hodgkin's", "adult non-Hodgkin's lymphoma, high grade, stage II", "non-Hodgkin's lymphoma, high grade, stage II adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II High Grade Adult Non-Hodgkin's Lymphoma", "shortest_name_length": 30}
{"curie": "MONDO:0009062", "names": ["Lubani Al Saleh Teebi syndrome", "Lubani-Al Saleh-Teebi syndrome", "Lubani Al-Saleh Teebi syndrome", "cystic fibrosis gastritis megaloblastic anemia", "Cystic fibrosis-gastritis-megaloblastic anemia syndrome", "cystic fibrosis-gastritis-megaloblastic anemia syndrome", "cystic fibrosis with gastritis and megaloblastic anemia syndrome", "Cystic fibrosis with gastritis and megaloblastic anemia syndrome", "Cystic fibrosis with gastritis and megaloblastic anaemia syndrome", "Cystic fibrosis with gastritis and megaloblastic anemia syndrome (disorder)", "cystic fibrosis with gastritis and megaloblastic anemia syndrome (diagnosis)", "cystic fibrosis with Helicobacter pylori gastritis, megaloblastic anemia, and mental retardation", "CYSTIC FIBROSIS WITH HELICOBACTER PYLORI GASTRITIS, MEGALOBLASTIC ANEMIA, AND MENTAL RETARDATION", "cystic fibrosis with Helicobacter pylori gastritis, megaloblastic anemia, and intellectual disability", "cystic fibrosis, Helicobacter pylori gastritis, megaloblastic anemia, subnormal mentality and minor anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cystic fibrosis-gastritis-megaloblastic anemia syndrome", "shortest_name_length": 30}
{"curie": "MONDO:0032911", "names": ["DFNA75", "deafness, autosomal dominant 75", "DEAFNESS, AUTOSOMAL DOMINANT 75", "hearing loss, autosomal dominant 75", "autosomal dominant nonsyndromic deafness 75"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal dominant 75", "shortest_name_length": 6}
{"curie": "UMLS:C1299564", "names": ["Posthemorrhagic hydrocephalus", "Posthaemorrhagic hydrocephalus", "Post-Hemorrhagic Hydrocephalus", "Post Hemorrhagic Hydrocephalus", "Post-hemorrhagic hydrocephalus", "Post-haemorrhagic hydrocephalus", "Posthemorrhagic hydrocephalus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Posthemorrhagic hydrocephalus", "shortest_name_length": 29}
{"curie": "MONDO:0002487", "names": ["breast granular cell tumor", "Breast Granular Cell Tumor", "granular cell tumor of breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast granular cell tumor", "shortest_name_length": 26}
{"curie": "MONDO:0014383", "names": ["TAM2", "tubular aggregate myopathy 2", "MYOPATHY, TUBULAR AGGREGATE, 2", "myopathy, tubular aggregate, 2", "ORAI1 tubular aggregate myopathy", "myopathy, tubular aggregate, type 2", "tubular aggregate myopathy caused by mutation in ORAI1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy, tubular aggregate, 2", "shortest_name_length": 4}
{"curie": "MONDO:0001703", "names": ["Colorblindness", "blindness color", "BLINDNESS COLOR", "Color blindness", "color blindness", "COLOR BLINDNESS", "Blindness color", "Color Blindness", "Blindness, Color", "Colour blindness", "colour blindness", "Blindness colour", "BLINDNESS COLOUR", "Color vision loss", "Color vision defect", "Color blindness NOS", "Color Vision Defect", "No color perception", "Vision Defect, Color", "Loss in color vision", "Colour blindness NOS", "Colour vision defect", "color vision defects", "No colour perception", "color-vision disease", "Color Vision Defects", "Defect, Color Vision", "Color vision defects", "Color blindness, NOS", "Abnormal color vision", "Impaired color vision", "color vision disorder", "IMPAIRED COLOR VISION", "Loss in colour vision", "Colour vision defects", "Colour blindness, NOS", "Defects, Color Vision", "Vision Defects, Color", "Disturbed color vision", "Defective color vision", "Abnormal colour vision", "Color vision disturbed", "color vision deficiency", "Blindness;colour vision", "Defective colour vision", "Color Vision Deficiency", "Color vision deficiency", "Deficiency, Color Vision", "colour vision deficiency", "DEFECTIVE COULOUR VISION", "Vision Deficiency, Color", "Deficiency;colour vision", "color blindness disorder", "Colour vision deficiency", "Color vision deficiencies", "Color Vision Deficiencies", "Deficiencies, Color Vision", "Colour vision deficiencies", "Color blindness (disorder)", "Abnormal color vision, NOS", "color blindness; blindness", "Color vision abnormalities", "blindness; color blindness", "Color Vision and Blindness", "Vision Deficiencies, Color", "Color vision defect, severe", "Abnormal colour vision, NOS", "Abnormality of color vision", "color blindness (diagnosis)", "Abnormality of colour vision", "Colour vision defect, severe", "Color vision deficiency, NOS", "uncategorized color blindness", "Colour vision deficiency, NOS", "Abnormal color vision (finding)", "Color vision deficiency (disorder)", "uncategorized color blindness (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "color vision disorder", "shortest_name_length": 14}
{"curie": "UMLS:C0268617", "names": ["homocystinemia", "Homocystinemia", "homocystinaemia", "Homocystinaemia", "Homocystinemia, NOS", "Homocystinemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Homocystinemia", "shortest_name_length": 14}
{"curie": "MONDO:0019757", "names": ["alobar holoprosencephaly", "Alobar Holoprosencephaly", "Alobar holoprosencephaly", "Holoprosencephaly, Alobar", "Alobar Holoprosencephalies", "Holoprosencephalies, Alobar", "HOLOPROSENCEPHALY, FAMILIAL ALOBAR", "Holoprosencephaly, Familial Alobar", "Alobar holoprosencephaly (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alobar holoprosencephaly", "shortest_name_length": 24}
{"curie": "MONDO:0042705", "names": ["Prostatic malacoplakia associated with prostatic abscess", "prostatic malacoplakia associated with prostatic abscess", "Prostatic malacoplakia with prostatic and seminal vesicle abscess", "prostatic malacoplakia with prostatic and seminal vesicle abscess"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostatic malacoplakia associated with prostatic abscess", "shortest_name_length": 56}
{"curie": "UMLS:C4553699", "names": ["Stage IV", "Stage IV Uterine Corpus Cancer AJCC v8", "Stage IV Uterine (including Endometrial) Cancer", "Stage IV Uterine Corpus Carcinoma or Carcinosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Uterine Corpus Cancer AJCC v8", "shortest_name_length": 8}
{"curie": "UMLS:C2981699", "names": ["Stage II Eyelid Carcinoma", "Stage II Eyelid Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Eyelid Carcinoma AJCC v7", "shortest_name_length": 25}
{"curie": "UMLS:C5400664", "names": ["EIA", "Endocrine Therapy-Related Alopecia", "Endocrine Therapy-Induced Alopecia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endocrine Therapy-Induced Alopecia", "shortest_name_length": 3}
{"curie": "MONDO:0018278", "names": ["CMD-MR", "CMD with intellectual disability", "congenital muscular dystrophy with intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital muscular dystrophy with intellectual disability", "shortest_name_length": 6}
{"curie": "UMLS:C5668172", "names": ["Heart FA-DLBCL", "Cardiac FA-DLBCL", "Heart Fibrin-Associated Diffuse Large B-Cell Lymphoma", "Cardiac Fibrin-Associated Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiac Fibrin-Associated Diffuse Large B-Cell Lymphoma", "shortest_name_length": 14}
{"curie": "MONDO:0013671", "names": ["HYDM2", "HYDATIDIFORM MOLE, COMPLETE", "hydatidiform Mole, complete", "hydatidiform mole, recurrent, 2", "hydatidiform MOLE, recurrent, 2", "HYDATIDIFORM MOLE, RECURRENT, 2", "KHDC3L complete hydatidiform mole", "hydatidiform Mole, recurrent, type 2", "complete hydatidiform mole caused by mutation in KHDC3L"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hydatidiform mole, recurrent, 2", "shortest_name_length": 5}
{"curie": "MONDO:0002881", "names": ["vagina adenosarcoma", "Vaginal Adenosarcoma", "vaginal adenosarcoma", "adenosarcoma of vagina", "vaginal Müllerian adenosarcoma", "vaginal Mullerian adenosarcoma", "Vaginal Mullerian Adenosarcoma", "Vaginal Müllerian Adenosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vaginal adenosarcoma", "shortest_name_length": 19}
{"curie": "UMLS:C0279649", "names": ["Acute Basophilic Leukemia", "childhood acute basophilic leukemia", "Pediatric Acute Basophilic Leukemia", "pediatric acute basophilic leukemia", "Childhood Acute Basophilic Leukemia", "basophilic leukemia, childhood acute", "leukemia, childhood acute basophilic", "acute basophilic leukemia, childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Acute Basophilic Leukemia", "shortest_name_length": 25}
{"curie": "MONDO:0019725", "names": ["SLE, pediatric onset", "pediatric systemic lupus erythematosus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pediatric systemic lupus erythematosus", "shortest_name_length": 20}
{"curie": "UMLS:C1300818", "names": ["necrotic tumor", "Necrotic tumor", "Necrotic tumour", "necrotic tumour", "Necrotic Neoplasm", "Necrotic tumor (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Necrotic tumor", "shortest_name_length": 14}
{"curie": "UMLS:C4744545", "names": ["Metastatic Vulvar Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Vulvar Carcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C1333950", "names": ["Helicobacter Pylori-Related Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Helicobacter Pylori-Related Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0044301", "names": ["AAT11", "AORTIC ANEURYSM, FAMILIAL THORACIC 11, SUSCEPTIBILITY TO", "aortic aneurysm, familial thoracic 11, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic aneurysm, familial thoracic 11, susceptibility to", "shortest_name_length": 5}
{"curie": "UMLS:C2347925", "names": ["Refractory Childhood Spinal Cord Tumor", "Refractory Childhood Spinal Cord Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Childhood Spinal Cord Neoplasm", "shortest_name_length": 38}
{"curie": "MONDO:0013936", "names": ["CG7", "CGB", "PBD6A", "peroxisome biogenesis disorder 6A", "Peroxisome Biogenesis Disorder 6A", "peroxisome biogenesis disorder 6A (Zellweger)", "PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER)", "PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP B", "peroxisome biogenesis disorder, complementation group B", "peroxisome biogenesis disorder, complementation group 7", "PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 7", "Peroxisome Biogenesis Disorder, Complementation Group B", "Peroxisome Biogenesis Disorder, Complementation Group 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder 6A (Zellweger)", "shortest_name_length": 3}
{"curie": "UMLS:C4553780", "names": ["Stage 0 Penile Cancer", "Stage 0 Penile Cancer AJCC v8", "Stage 0 Penile Squamous Cell Carcinoma AJCC v8", "Stage 0 Squamous Cell Carcinoma of the Penis AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Penile Cancer AJCC v8", "shortest_name_length": 21}
{"curie": "UMLS:C5446635", "names": ["Breast Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Neuroendocrine Carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0003802", "names": ["cornea cancer", "corneal tumor", "Corneal tumor", "cancer of cornea", "neoplasm of cornea", "Malignant Cornea Tumor", "malignant cornea tumor", "malignant corneal tumor", "Malignant Corneal Tumor", "malignant Corneal tumor", "Malignant tumor of cornea", "Malignant Tumor of Cornea", "malignant cornea neoplasm", "Malignant Cornea Neoplasm", "malignant tumor of cornea", "Malignant Corneal Neoplasm", "Malignant tumour of cornea", "malignant corneal neoplasm", "Malignant neoplasm of cornea", "malignant neoplasm of cornea", "Malignant Neoplasm of Cornea", "Malignant Tumor of the Cornea", "malignant tumor of the cornea", "Malignant Neoplasm of the Cornea", "malignant neoplasm of the cornea", "Malignant tumor of cornea (disorder)", "malignant neoplasm of cornea (primary)", "malignant neoplasm of cornea (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cornea cancer", "shortest_name_length": 13}
{"curie": "MONDO:0013913", "names": ["HH11", "TACR3 hypogonadotropic hypogonadism", "hypogonadotropic hypogonadism 11 with or without anosmia", "HYPOGONADOTROPIC HYPOGONADISM 11 WITH OR WITHOUT ANOSMIA", "hypogonadotropic hypogonadism caused by mutation in TACR3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadotropic hypogonadism 11 with or without anosmia", "shortest_name_length": 4}
{"curie": "MONDO:0019265", "names": ["diazoxide-resistant focal hyperinsulinism", "hyperinsulinemic hypoglycemia, diazoxide-resistant focal form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diazoxide-resistant focal hyperinsulinism", "shortest_name_length": 41}
{"curie": "UMLS:C0855151", "names": ["Stage IV B-Lymphoblastic Lymphoma", "Stage IV B Lymphoblastic Lymphoma", "Precursor B-Lymphoblastic Lymphoma Stage IV", "Precursor B-lymphoblastic lymphoma stage IV", "Stage IV Precursor B-Lymphoblastic Lymphoma", "Ann Arbor Stage IV B Lymphoblastic Lymphoma", "Precursor B-lymphoblastic lymphoma NOS stage IV"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Precursor B-lymphoblastic lymphoma stage IV", "shortest_name_length": 33}
{"curie": "UMLS:C1370970", "names": ["stage A prostate cancer", "Prostate cancer stage A", "Stage A Prostate Cancer", "prostate cancer, stage A", "Stage A Prostate Carcinoma", "stage A cancer of the prostate", "cancer of the prostate, stage A", "stage A carcinoma of the prostate", "carcinoma of the prostate, stage A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate cancer stage A", "shortest_name_length": 23}
{"curie": "MONDO:0019284", "names": ["isolated nail anomaly", "nonsyndromic nail anomaly", "inherited isolated nail anomaly", "nonsyndromic congenital nail disorder", "nail disorder, nonsyndromic congenital"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited isolated nail anomaly", "shortest_name_length": 21}
{"curie": "UMLS:C0279954", "names": ["Stage I", "Grade I Follicular Lymphoma Stage I", "stage I grade 1 follicular lymphoma", "Stage I Grade I Follicular Lymphoma", "Stage I Grade 1 Follicular Lymphoma", "Ann Arbor Stage I Grade 1 Follicular Lymphoma", "Follicular Small Cleaved Cell Lymphoma Stage I", "Stage I Follicular Small Cleaved Cell Lymphoma", "stage I follicular small cleaved cell lymphoma", "follicular small cleaved cell lymphoma, stage I", "Stage I Grade I Follicular Small Cleaved Cell Lymphoma", "stage I grade I follicular small cleaved cell lymphoma", "Grade I Follicular Small Cleaved Cell Lymphoma Stage I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage I Grade 1 Follicular Lymphoma", "shortest_name_length": 7}
{"curie": "UMLS:C2931383", "names": ["Chromosomal mosaicism due to mitotic instability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chromosomal mosaicism due to mitotic instability", "shortest_name_length": 48}
{"curie": "MONDO:0002615", "names": ["Xanthomata", "xanthomatosis", "Xanthomatosis", "XANTHOMATOSIS", "Xanthomatoses", "xanthelasmatosis", "Xanthomatosis, NOS", "xanthomatosis (disease)", "Xanthomatosis (disorder)", "Yellow bumps of fatty deposits on skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "xanthomatosis", "shortest_name_length": 10}
{"curie": "MONDO:0001106", "names": ["ESRD", "Renal failure", "renal failure", "Renal Failure", "RENAL FAILURE", "failure; renal", "KIDNEY FAILURE", "failure, renal", "Failure, Renal", "Kidney failure", "Kidney Failure", "Renal Failures", "renal; failure", "Failure kidney", "kidney failure", "FAILURE KIDNEY", "Failures, Renal", "Kidney Failures", "kidney; failure", "Failure, Kidney", "Renal impairment", "Renal Impairment", "renal impairment", "Failures, Kidney", "impairment renal", "Renal failure NOS", "Renal dysfunction", "RENAL FAILURE NOS", "Kidney Impairment", "impairments renal", "Failure;renal;NOS", "RF - Renal failure", "Insufficiency renal", "renal insufficiency", "INSUFFICIENCY RENAL", "RENAL INSUFFICIENCY", "Renal insufficiency", "Renal Insufficiency", "Insufficiency;renal", "Renal impairment NOS", "Kidney Insufficiency", "insufficiency; renal", "kidney insufficiency", "renal insufficiencies", "Insufficiency, Kidney", "Renal Insufficiencies", "kidney; insufficiency", "Kidney Insufficiencies", "renal failure syndrome", "Renal Failure Syndrome", "syndrome renal failure", "Renal failure syndrome", "Impaired renal function", "function impaired renal", "impaired renal function", "renal failure (diagnosis)", "Renal failure unspecified", "Unspecified renal failure", "Renal failure, unspecified", "Unspecified kidney failure", "Renal failure in adulthood", "Renal failure syndrome, NOS", "Renal impairment (disorder)", "Renal impairment (diagnosis)", "Renal insufficiency syndrome", "Renal insufficiency (disorder)", "renal insufficiency (diagnosis)", "renal disorders renal impairment", "Renal failure syndrome (disorder)", "Renal insufficiency syndrome, NOS", "renal failure not otherwise specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kidney failure", "shortest_name_length": 4}
{"curie": "UMLS:C5239591", "names": ["Refractory Gliosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Gliosarcoma", "shortest_name_length": 22}
{"curie": "MONDO:0019168", "names": ["PM", "Pyomyositis", "PYOMYOSITIS", "pyomyositis", "tropical myositis", "Tropical Myositis", "Tropical myositis", "myositis tropicans", "Myositis tropicans", "Myositis, Tropical", "Suppurative myositis", "Tropical pyomyositis", "tropical pyomyositis", "suppurative myositis", "Tropical Pyomyositis", "PYOMYOSITIS, TROPICAL", "Myositis purulenta tropica", "myositis purulenta tropica", "Tropical pyomyositis (disorder)", "MYOSITIS, BACTERIAL, SPONTANEOUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyomyositis", "shortest_name_length": 2}
{"curie": "MONDO:0018378", "names": ["ONJ", "Jaw Osteonecrosis", "jaw osteonecrosis", "osteonecrosis; jaw", "jaw; osteonecrosis", "necrosis; bone, jaw", "bone; necrosis, jaw", "Osteonecrosis of jaw", "osteonecrosis of jaw", "Osteonecrosis of Jaw", "aseptic necrosis of jaw", "Aseptic necrosis of jaw", "Necrosis of bone of jaw", "Osteonecrosis of the jaw", "osteonecrosis of the jaw", "Aseptic necrosis of bone, jaw", "Aseptic necrosis of bone of jaw", "Necrosis of bone of jaw (disorder)", "aseptic necrosis of jaw (diagnosis)", "Aseptic necrosis of bone of jaw (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteonecrosis of the jaw", "shortest_name_length": 3}
{"curie": "MONDO:0017300", "names": ["anomaly; pericardium", "pericardium; anomaly", "pericardium; deformity", "deformity; pericardium", "Congenital pericardium anomaly", "congenital pericardium anomaly", "Congenital anomaly of pericardium", "Congenital anomaly of pericardium, NOS", "Congenital anomaly of pericardium (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital pericardium anomaly", "shortest_name_length": 20}
{"curie": "MONDO:0001530", "names": ["Secondary renal hyperparathyroidism", "renal secondary hyperparathyroidism", "hyperparathyroidism; secondary, renal", "secondary; hyperparathyroidism, renal", "secondary hyperparathyroidism of renal origin", "Secondary hyperparathyroidism of renal origin", "hyperparathyroidism due to renal insufficiency", "Hyperparathyroidism due to renal insufficiency", "Secondary hyperparathyroidism (of renal origin)", "secondary hyperparathyroidism (of renal origin)", "secondary hyperparathyroidism due to renal causes", "Hyperparathyroidism due to renal insufficiency (disorder)", "secondary hyperparathyroidism due to renal causes (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary hyperparathyroidism of renal origin", "shortest_name_length": 35}
{"curie": "UMLS:C0334228", "names": ["SMALL CELL TUMOR MALIGNANT", "Malignant Tumor, Small Cell Type", "Malignant tumor, small cell type", "Malignant tumor - small cell type", "Malignant tumour, small cell type", "Malignant tumour - small cell type", "tumor; malignant, small cell (type)", "tumor; small cell (type), malignant", "Malignant tumor, small cell type (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant tumor, small cell type", "shortest_name_length": 26}
{"curie": "MONDO:0017136", "names": ["omodysplasia", "Omodysplasia", "Omodysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "omodysplasia", "shortest_name_length": 12}
{"curie": "UMLS:C4526713", "names": ["Stage I", "Stage I Lung Cancer", "Stage I Lung Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Lung Cancer AJCC v8", "shortest_name_length": 7}
{"curie": "UMLS:C0153303", "names": ["Mixed helminthiasis NOS", "helminthiasis; mixed types", "mixed; helminthiasis (types)", "mixed intestinal helminthiasis", "Mixed intestinal helminthiasis", "Mixed intestinal helminthiases", "Infection by intestinal helminths", "mixed intestinal helminthiasis (diagnosis)", "Mixed intestinal infection due to Class Cestoda and/or Class Trematoda and/or Phylum Nemata", "Mixed intestinal infection caused by Class Cestoda and/or Class Trematoda and/or Phylum Nemata", "Mixed intestinal infection caused by Class Cestoda and/or Class Trematoda and/or Phylum Nemata (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mixed intestinal helminthiasis", "shortest_name_length": 23}
{"curie": "MONDO:0032729", "names": ["MRT70", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 70", "Mental Retardation, Autosomal Recessive 70", "autosomal recessive intellectual developmental disorder 70", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 70", "intellectual developmental disorder, autosomal recessive 70"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder, autosomal recessive 70", "shortest_name_length": 5}
{"curie": "MONDO:0009610", "names": ["MGA1", "MGCA1", "MGA type I", "MGA, TYPE I", "Mga, type 1", "MGA, Type I", "3-MGCA type I (3-MGCA-1)", "3MG CoA hydratase deficiency", "3MG-CoA hydratase deficiency", "3-MG-CoA-HYDRATASE DEFICIENCY", "3-Mg-Coa-hydratase deficiency", "3-Mg-CoA-Hydratase Deficiency", "auh 3-methylglutaconic aciduria", "AUH 3-methylglutaconic aciduria", "3 methylglutaconic aciduria type 1", "3-methylglutaconic aciduria type 1", "3-Methylglutaconic Aciduria Type 1", "3-methylglutaconic aciduria type I", "3-Methylglutaconic aciduria type 1", "3-Methylglutaconic aciduria, type 1", "3-METHYLGLUTACONIC aciduria, type I", "3-Methylglutaconic Aciduria, Type I", "3-METHYLGLUTACONIC ACIDURIA, TYPE I", "3-@METHYLGLUTACONIC ACIDURIA, TYPE I", "3 alpha methylglutaconic aciduria type I", "3-methylglutaconyl-Coa hydratase deficiency", "3-methylglutaconyl-CoA hydratase deficiency", "3-Methylglutaconyl-CoA Hydratase Deficiency", "3-METHYLGLUTACONYL-CoA HYDRATASE DEFICIENCY", "3 methylglutaconyl CoA hydratase deficiency", "3-Methylglutaconic aciduria type 1 (disorder)", "3-methylglutaconic aciduria caused by mutation in AUH", "3-methylglutaconic aciduria caused by mutation in auh", "3-methylglutaconyl-CoA hydratase deficiency (auh defect)", "3-Methylglutaconyl-CoA hydratase deficiency with 3-methylglutaconic acid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "3-methylglutaconic aciduria type 1", "shortest_name_length": 4}
{"curie": "MONDO:0012363", "names": ["RP32", "Retinitis Pigmentosa 32", "RETINITIS PIGMENTOSA 32", "retinitis pigmentosa 32", "retinitis pigmentosa type 32"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 32", "shortest_name_length": 4}
{"curie": "MONDO:0023170", "names": ["focal or multifocal malformations in neuronal migration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal or multifocal malformations in neuronal migration", "shortest_name_length": 55}
{"curie": "MONDO:0035782", "names": ["Non-syndromic ARM with rectobulbar fistula", "Non-syndromic ARM with rectourethral fistula, bulbar type", "Non-syndromic anorectal malformation with rectobulbar fistula", "non-syndromic anorectal malformation with rectourethral fistula, bulbar type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-syndromic anorectal malformation with rectourethral fistula, bulbar type", "shortest_name_length": 42}
{"curie": "MONDO:0017296", "names": ["glycerol kinase deficiency, adult form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycerol kinase deficiency, adult form", "shortest_name_length": 38}
{"curie": "UMLS:C5552715", "names": ["AN", "ANUBP", "AN/ANUBP", "Atypical Neurofibroma", "Atypical Neurofibromatous Neoplasm of Uncertain Biologic Potential", "Atypical Neurofibromatous Neoplasm with Uncertain Biologic Potential"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypical Neurofibromatous Neoplasm of Uncertain Biologic Potential", "shortest_name_length": 2}
{"curie": "MONDO:0014584", "names": ["CMS3B", "congenital myasthenic syndrome 3B", "congenital myasthenic syndrome type 3B", "congenital myasthenic syndrome 3B, fast-channel", "MYASTHENIC SYNDROME, CONGENITAL, 3B, FAST-CHANNEL", "myasthenic syndrome, congenital, 3B, FAST-channel"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myasthenic syndrome 3B", "shortest_name_length": 5}
{"curie": "MONDO:0011521", "names": ["IBD7", "INFLAMMATORY BOWEL DISEASE 7", "inflammatory bowel disease 7", "Inflammatory Bowel Disease 7", "inflammatory bowel disease type 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory bowel disease 7", "shortest_name_length": 4}
{"curie": "UMLS:C5204069", "names": ["Prostate Neuroendocrine Carcinoma", "Neuroendocrine carcinoma of prostate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neuroendocrine carcinoma of prostate", "shortest_name_length": 33}
{"curie": "MONDO:0011263", "names": ["SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL", "skeletal dysplasia and progressive central nervous system degeneration, lethal", "Skeletal Dysplasia And Progressive Central Nervous System Degeneration, Lethal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skeletal dysplasia and progressive central nervous system degeneration, lethal", "shortest_name_length": 78}
{"curie": "MONDO:0013503", "names": ["CANDF6", "candidiasis, familial, 6", "CANDIDIASIS, FAMILIAL, 6", "candidiasis, familial, type 6", "candidiasis, familial, 6, autosomal dominant", "IL17F familial chronic mucocutaneous candidiasis", "CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL DOMINANT", "candidiasis, familial chronic mucocutaneous, autosomal dominant", "familial chronic mucocutaneous candidiasis caused by mutation in IL17F"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "candidiasis, familial, 6", "shortest_name_length": 6}
{"curie": "MONDO:0003279", "names": ["testicular infarct", "Testicular infarct", "infarction of testis", "Infarction of testis", "Testicular Infarction", "testicular infarction", "Testicular infarction", "infarctions testicular", "Infarction of testis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular infarct", "shortest_name_length": 18}
{"curie": "MONDO:0009500", "names": ["susceptibility to kuru", "KURU, SUSCEPTIBILITY TO", "kuru, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kuru, susceptibility to", "shortest_name_length": 22}
{"curie": "MONDO:0008519", "names": ["SYNS1", "Wl syndrome", "WL SYNDROME", "multiple synostoses syndrome 1", "MULTIPLE SYNOSTOSES SYNDROME 1", "Multiple synostoses syndrome 1", "Facioaudiosymphalangism syndrome", "nog multiple synostoses syndrome", "facioaudiosymphalangism syndrome", "NOG multiple synostoses syndrome", "FACIOAUDIOSYMPHALANGISM SYNDROME", "multiple synostoses syndrome type 1", "SYMPHALANGISM-BRACHYDACTYLY SYNDROME", "Symphalangism-brachydactyly syndrome", "symphalangism-brachydactyly syndrome", "symphalangism brachydactyly syndrome", "synostoses multiple with brachydactyly", "SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY", "Synostoses, multiple, with brachydactyly", "synostoses, multiple, with brachydactyly", "Deafness-symphalangism syndrome of Herrmann", "deafness-symphalangism syndrome of Herrmann", "DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN", "multiple synostoses syndrome caused by mutation in nog", "multiple synostoses syndrome caused by mutation in NOG"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple synostoses syndrome 1", "shortest_name_length": 5}
{"curie": "MONDO:0100311", "names": ["sensory ataxia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sensory ataxia", "shortest_name_length": 14}
{"curie": "UMLS:C1333940", "names": ["Head and Neck Basaloid Carcinoma", "Head and Neck Basaloid Squamous Cell Carcinoma", "Basaloid Squamous Cell Carcinoma of Head and Neck", "Basaloid Squamous Cell Carcinoma of the Head and Neck"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Head and Neck Basaloid Carcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C1334743", "names": ["Metastatic Squamous Cell Breast Carcinoma", "Metastatic Breast Squamous Cell Carcinoma", "Metastatic Squamous Cell Carcinoma of Breast", "Metastatic Squamous Cell Carcinoma of the Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Breast Squamous Cell Carcinoma", "shortest_name_length": 41}
{"curie": "UMLS:C4524751", "names": ["Postneoadjuvant Therapy Stage IVB Gastroesophageal Junction Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postneoadjuvant Therapy Stage IVB Gastroesophageal Junction Adenocarcinoma AJCC v8", "shortest_name_length": 82}
{"curie": "UMLS:C0264909", "names": ["intraventricular block", "INTRAVENTRICULAR BLOCK", "Intraventricular block", "block; intraventricular", "intraventricular; block", "Intraventricular block NOS", "Intraventricular block, NOS", "HEART BLOCK INTRAVENTRICULAR", "Heart block intraventricular", "Intraventricular conduction delay", "intraventricular conduction delay", "DEFECT CONDUCTION INTRAVENTRICULAR", "Intraventricular conduction defect", "Defect conduction intraventricular", "Intraventricular conduction defect, NOS", "Intraventricular conduction defect (disorder)", "intraventricular conduction delay (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraventricular conduction defect", "shortest_name_length": 22}
{"curie": "MONDO:0054785", "names": ["MMDS6", "PMPCB deficiency", "multiple mitochondrial dysfunctions syndrome 6", "MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 6", "Multiple mitochondrial dysfunctions syndrome type 6", "multiple mitochondrial dysfunctions syndrome type 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple mitochondrial dysfunctions syndrome 6", "shortest_name_length": 5}
{"curie": "UMLS:C1336910", "names": ["Endometrial Endometrioid Adenocarcinoma with Papillae"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endometrial Endometrioid Adenocarcinoma with Papillae", "shortest_name_length": 53}
{"curie": "MONDO:0018921", "names": ["Meckel-Gruber", "Meckel syndrome", "meckel gruber syndrome", "Meckel-Gruber syndrome", "Meckel-Gruber Syndrome", "meckel-gruber syndrome", "Meckel syndrome (diagnosis)", "Dysencephalia splanchnocystica", "dysencephalia splanchnocystica", "Meckel-Gruber syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meckel syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0100225", "names": ["collagen 6-related myopathy", "collagen VI-related myopathy", "collagen VI-related muscle disorder", "collagen VI-related muscular dystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "collagen 6-related myopathy", "shortest_name_length": 27}
{"curie": "MONDO:0001293", "names": ["subglottis cancer", "cancer of subglottis", "Ca larynx - subglottis", "Malignant Subglottis Tumor", "malignant subglottic tumor", "malignant subglottis tumor", "Malignant Subglottic Tumor", "malignant Subglottic tumor", "malignant subglottal neoplasm", "Malignant Subglottis Neoplasm", "malignant subglottis neoplasm", "Malignant tumor of subglottis", "malignant subglottic neoplasm", "malignant tumor of subglottis", "Malignant Tumor of Subglottis", "Malignant Subglottic Neoplasm", "Malignant tumour of subglottis", "Malignant neoplasm of subglottis", "Malignant Neoplasm of Subglottis", "malignant neoplasm of subglottis", "Malignant Tumor of the Subglottis", "malignant tumor of the subglottis", "Malignant Neoplasm of the Subglottis", "malignant neoplasm of the subglottis", "Malignant tumor of subglottis (disorder)", "malignant neoplasm of subglottis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subglottis cancer", "shortest_name_length": 17}
{"curie": "UMLS:C1334321", "names": ["Kaposi Sarcoma NCI Grade 3", "Kaposi's Sarcoma NCI Grade 3", "Kaposi's Sarcoma NCI Grade III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kaposi Sarcoma NCI Grade 3", "shortest_name_length": 26}
{"curie": "UMLS:C3536739", "names": ["Thoracic meningomyelocele", "Thoracic Myelomeningocele", "thoracic meningomyelocele", "Thoracic Meningomyelocele", "Thoracic meningomyelocele (disorder)", "thoracic meningomyelocele (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thoracic meningomyelocele", "shortest_name_length": 25}
{"curie": "MONDO:0011468", "names": ["HMSNP", "HMSNO", "HMSNP, FORMERLY", "Hereditary motor and sensory neuropathy Okinawa type", "hereditary motor and sensory neuropathy, Okinawa type", "Hereditary motor and sensory neuropathy, Okinawa type", "HEREDITARY MOTOR AND SENSORY NEUROPATHY, OKINAWA TYPE", "Hereditary motor and sensory neuropathy proximal type", "Neuropathy, hereditary motor and sensory, Okinawa type", "HEREDITARY MOTOR AND SENSORY NEUROPATHY, PROXIMAL TYPE", "NEUROPATHY, HEREDITARY MOTOR AND SENSORY, OKINAWA TYPE", "neuropathy, hereditary motor and sensory, Okinawa type", "Hereditary motor and sensory neuropathy, proximal type", "hereditary motor and sensory neuropathy, proximal type", "Hereditary motor and sensory neuropathy Okinawa type (disorder)", "HEREDITARY MOTOR AND SENSORY NEUROPATHY, PROXIMAL TYPE, FORMERLY", "hereditary motor and sensory neuropathy, proximal type, formerly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary motor and sensory neuropathy, Okinawa type", "shortest_name_length": 5}
{"curie": "UMLS:C0751733", "names": ["degenerative spinal cord disease", "cord degenerative disease spinal", "spinal cord degenerative diseases", "Degenerative Diseases, Spinal Cord"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Degenerative Diseases, Spinal Cord", "shortest_name_length": 32}
{"curie": "MONDO:0005916", "names": ["Placenta acreta", "Placenta Accreta", "placenta Increta", "PLACENTA ACCRETA", "Placenta accreta", "placenta accreta", "accreta placenta", "Accreta, Placenta", "Increta, placenta", "placenta; accreta", "accreta; placenta", "placenta Percreta", "accreta, placenta", "Percreta, placenta", "Placenta accreta, NOS", "Placenta accreta (disorder)", "placenta accreta (diagnosis)", "placenta accreta was observed", "placenta accreta (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "placenta accreta", "shortest_name_length": 15}
{"curie": "MONDO:0001117", "names": ["METHEMOGLOBINEMIA", "methemoglobinemia", "Methemoglobinemia", "Methemoglobinemias", "methemoglobinemias", "methaemoglobinaemia", "METHAEMOGLOBINAEMIA", "Methaemoglobinaemia", "Methemoglobinemia NOS", "Methemoglobinemia, NOS", "Increased methemoglobin", "Methaemoglobinaemia NOS", "Increased methaemoglobin", "Methemoglobinemia (disorder)", "methemoglobinemia (diagnosis)", "Methemoglobinemia, unspecified", "Methaemoglobinaemia, unspecified", "Methemoglobin above reference range", "Methaemoglobin above reference range", "Methemoglobin above reference range (finding)", "Methemoglobin concentration increased above normal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "methemoglobinemia", "shortest_name_length": 17}
{"curie": "UMLS:C5204281", "names": ["Lower pole", "Lower Pole Kidney Tumor", "Kidney Tumor, Lower Pole"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kidney Tumor, Lower Pole", "shortest_name_length": 10}
{"curie": "MONDO:0002083", "names": ["RICHTER SYNDROME", "Richter syndrome", "richter syndrome", "Richter Syndrome", "richters syndrome", "richter's syndrome", "Richter's syndrome", "Richter's Syndrome", "Richter transformation", "Richter's Transformation", "Richter's transformation", "Richter's syndrome (disorder)", "Richter's syndrome (diagnosis)", "leukemia lymphocytic Richter's syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Richter syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0032794", "names": ["LCA19", "Leber congenital amaurosis 19", "leber congenital amaurosis 19", "LEBER CONGENITAL AMAUROSIS 19"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leber congenital amaurosis 19", "shortest_name_length": 5}
{"curie": "UMLS:C5205620", "names": ["Platinum-Sensitive Fallopian Tube Cancer", "Platinum-Sensitive Fallopian Tube Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Platinum-Sensitive Fallopian Tube Carcinoma", "shortest_name_length": 40}
{"curie": "UMLS:C4744444", "names": ["Metastatic Lung Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Lung Adenocarcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0008675", "names": ["FSS", "DA2A", "Whistling face", "whistling face", "Freeman-Sheldon", "Whistling face syndrome", "whistling-face syndrome", "Freeman-Burian syndrome", "whistling face syndrome", "Whistling-Face Syndrome", "Whistling Face Syndrome", "freeman sheldon syndrome", "Freeman-Sheldon syndrome", "FREEMAN-SHELDON SYNDROME", "Freeman Sheldon syndrome", "whistling face; syndrome", "freeman-sheldon syndrome", "Freeman-Sheldon Syndrome", "Freeman Sheldon Syndrome", "syndrome; whistling face", "craniocarpotarsal dysplasia", "Craniocarpotarsal dysplasia", "windmill-vane-hand syndrome", "craniocarpotarsal dystrophy", "Craniocarpotarsal dystrophy", "Craniocarpotarsal Dysplasia", "CRANIOCARPOTARSAL DYSTROPHY", "Windmill-Vane-Hand Syndrome", "CRANIOCARPOTARSAL DYSPLASIA", "cranio-carpo-tarsal syndrome", "Cranio-Carpo-Tarsal Syndrome", "Distal arthrogryposis type 2A", "Distal Arthrogryposis Type 2A", "arthrogryposis distal type 2a", "arthrogryposis distal type 2A", "distal arthrogryposis type 2A", "Distal Arthrogryposis, Type 2A", "arthrogryposis, distal, type 2A", "ARTHROGRYPOSIS, DISTAL, TYPE 2A", "Arthrogryposis, Distal, Type 2A", "Freeman-Sheldon syndrome (disorder)", "arthrogryposis distal type 2a (diagnosis)", "whistling face-windmill vane hand syndrome", "WHISTLING FACE-WINDMILL VANE HAND SYNDROME", "Whistling Face-Windmill Vane Hand Syndrome", "distal arthrogryposis type 2A (Freeman-Sheldon)", "arthrogryposis, distal, type 2A (Freeman-Sheldon)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Freeman-Sheldon syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C1336182", "names": ["Stage IIB Esophageal Squamous Cell Cancer", "Stage IIB Esophagus Squamous Cell Carcinoma", "Stage IIB Esophageal Squamous Cell Carcinoma", "Stage IIB Squamous Cell Carcinoma of Esophagus", "Stage IIB Squamous Cell Carcinoma of the Esophagus", "Stage IIB Esophageal Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Esophageal Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 41}
{"curie": "UMLS:C0334308", "names": ["adenocarcinoma in situ in tubulovillous adenoma", "Adenocarcinoma in situ in tubulovillous adenoma", "Adenocarcinoma In Situ in Tubulovillous Adenoma", "[M] Adenocarcinoma in situ in tubulovillous adenoma", "adenocarcinoma in situ in tubulovillous adenoma (diagnosis)", "Adenocarcinoma in situ in tubulovillous adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma in situ in tubulovillous adenoma", "shortest_name_length": 47}
{"curie": "MONDO:0011103", "names": ["NSRD1", "DFNA3", "DFNA3A", "autosomal dominant deafness 3A", "deafness, autosomal dominant 3a", "Deafness, Autosomal Dominant 3A", "deafness, autosomal dominant 3A", "DEAFNESS, AUTOSOMAL DOMINANT 3A", "deafness, autosomal dominant type 3A", "autosomal dominant nonsyndromic deafness 3A", "neurosensory nonsyndromic dominant deafness 1", "GJB2 autosomal dominant nonsyndromic deafness", "autosomal dominant nonsyndromic hearing loss 3A", "autosomal dominant nonsyndromic deafness type 3A", "deafness, autosomal dominant nonsyndromic sensorineural 3", "autosomal dominant nonsyndromic deafness caused by mutation in GJB2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 3A", "shortest_name_length": 5}
{"curie": "UMLS:C1320183", "names": ["Infection due to enterococcus", "Infection caused by enterococcus", "Infection caused by enterococcus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infection due to enterococcus", "shortest_name_length": 29}
{"curie": "MONDO:0020445", "names": ["absence of the SVC", "Absence of the SVC", "agenesis of the SVC", "Agenesis of the SVC", "Absence of superior vena cava", "absence of the superior vena cava", "Absence of the superior vena cava", "absence of the superior caval vein", "agenesis of the superior vena cava", "Absence of the superior caval vein", "Agenesis of the superior vena cava", "agenesis of the superior caval vein", "Agenesis of the superior caval vein", "Absence of superior vena cava (disorder)", "Congenital absence of superior vena cava", "Congenital absence of superior vena cava (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "agenesis of the superior vena cava", "shortest_name_length": 18}
{"curie": "MONDO:0010101", "names": ["TBSH", "Teebi Shaltout syndrome", "Teebi-Shaltout Syndrome", "Teebi-Shaltout syndrome", "TEEBI-SHALTOUT SYNDROME", "Teebi Shaltout syndrome (disorder)", "CRANIOFACIAL ANOMALIES, ABNORMAL HAIR, CAMPTODACTYLY, AND CAUDAL APPENDAGE", "craniofacial anomalies, abnormal hair, camptodactyly, and caudal appendage", "Craniofacial anomalies, abnormal hair, camptodactyly, and caudal appendage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Teebi-Shaltout syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0009825", "names": ["OPLAHD", "5-oxoprolinase deficiency", "5-OXOPROLINASE DEFICIENCY", "5-Oxoprolinase deficiency", "5-@OXOPROLINASE DEFICIENCY", "Reduced 5-oxoprolinase level", "5-alpha-oxoprolinase deficiency", "Pyroglutamate hydrolase deficiency", "5-oxoprolinase deficiency (disease)", "5-Oxoprolinase deficiency (disorder)", "Oxoprolinuria due to oxoprolinase deficiency", "oxoprolinuria due to oxoprolinase deficiency", "Oxoprolinuria Due To Oxoprolinase Deficiency", "oxoprolinuria due to 5-oxoprolinase deficiency", "Oxoprolinuria due to 5-oxoprolinase deficiency", "OXOPROLINURIA DUE TO 5-OXOPROLINASE DEFICIENCY", "inborn error of 5-oxoprolinase (ATP-hydrolyzing) activity", "inborn 5-oxoprolinase (ATP-hydrolyzing) activity disorder", "rare inborn error of 5-oxoprolinase (ATP-hydrolyzing) activity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "5-oxoprolinase deficiency", "shortest_name_length": 6}
{"curie": "MONDO:0012016", "names": ["CMAVM", "Cm-Avm", "CM-AVM", "CM-AVM syndrome", "Capillary malformation-arteriovenous malformation", "CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION", "Capillary Malformation-Arteriovenous Malformation", "capillary malformation-arteriovenous malformation", "capillary malformation without arteriovenous malformation", "capillary malformation-arteriovenous malformation syndrome", "Capillary Malformation-Arteriovenous Malformation Syndrome", "Capillary malformation-arteriovenous malformation syndrome", "CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION (disorder)", "Cmavm Capillary malformation arteriovenous malformation syndrome", "Cm-Avm Capillary malformation-arteriovenous malformation syndrome", "Capillary malformation-arteriovenous malformation syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "capillary malformation-arteriovenous malformation syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0013833", "names": ["KTCN7", "keratoconus 7", "KERATOCONUS 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratoconus 7", "shortest_name_length": 5}
{"curie": "MONDO:0013368", "names": ["MDNS", "MDN syndrome", "MAMMARY-DIGITAL-NAIL SYNDROME", "Mammary-digital-nail syndrome", "Mammary digital nail syndrome", "mammary-digital-nail syndrome", "Onycho-digito-mammary syndrome", "onycho-digito-mammary syndrome", "MDN (mammary digital nail) syndrome", "Mammary digital nail syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mammary-digital-nail syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0001688", "names": ["toxic neuropathy optic", "Toxic Optic Neuropathy", "toxic optic neuropathy", "Toxic optic neuropathy", "Optic Neuropathy, Toxic", "Neuropathy, Toxic Optic", "Toxic Optic Neuropathies", "Toxic optic neuropathy (disorder)", "toxic optic neuropathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "toxic optic neuropathy", "shortest_name_length": 22}
{"curie": "MONDO:0014525", "names": ["COXPD23", "combined oxidative phosphorylation deficiency 23", "Combined Oxidative Phosphorylation Deficiency 23", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 23", "Combined oxidative phosphorylation defect type 23", "combined oxidative phosphorylation defect type 23", "GTPBP3 combined oxidative phosphorylation deficiency", "combined oxidative phosphorylation deficiency type 23", "COXPD23 - combined oxidative phosphorylation defect type 23", "Combined oxidative phosphorylation defect type 23 (disorder)", "combined oxidative phosphorylation deficiency caused by mutation in GTPBP3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation defect type 23", "shortest_name_length": 7}
{"curie": "MONDO:0014045", "names": ["CWS3", "Cowden syndrome 3", "SDHD Cowden disease", "Cowden syndrome type 3", "Cowden disease caused by mutation in SDHD"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cowden syndrome 3", "shortest_name_length": 4}
{"curie": "UMLS:C4331321", "names": ["Stage II Hypopharyngeal Throat Cancer", "Stage II Hypopharyngeal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Hypopharyngeal Carcinoma AJCC v8", "shortest_name_length": 37}
{"curie": "UMLS:C0268830", "names": ["urethrotrigonitis", "Urethrotrigonitis", "Urethrotrigonitis (disorder)", "urethrotrigonitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urethrotrigonitis", "shortest_name_length": 17}
{"curie": "MONDO:0027687", "names": ["raltegravir toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "raltegravir toxicity", "shortest_name_length": 20}
{"curie": "UMLS:C4524852", "names": ["Refractory Primary Amyloidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Primary Amyloidosis", "shortest_name_length": 30}
{"curie": "MONDO:0018688", "names": ["anti-p200 pemphigoid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anti-p200 pemphigoid", "shortest_name_length": 20}
{"curie": "UMLS:C1384407", "names": ["Metaplastic meningioma", "Metaplastic Meningioma", "Metaplastic meningioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metaplastic meningioma", "shortest_name_length": 22}
{"curie": "UMLS:C1997351", "names": ["left cardiac ventricle dysfunction", "Left ventricular cardiac dysfunction", "myocardial dysfunction left cardiac ventricle", "left cardiac ventricle dysfunction (diagnosis)", "Left ventricular cardiac dysfunction (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Left ventricular cardiac dysfunction", "shortest_name_length": 34}
{"curie": "MONDO:0020790", "names": ["HGPPS", "HGPPS1", "Ophthalmoplegia, Progressive External, and Scoliosis", "GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS 1", "gaze palsy, familial horizontal, with progressive scoliosis 1", "GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS, 1", "gaze palsy, familial horizontal, with progressive scoliosis, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gaze palsy, familial horizontal, with progressive scoliosis 1", "shortest_name_length": 5}
{"curie": "UMLS:C1384489", "names": ["Scratch", "Scratched", "Scratches", "Scratch mark", "Scratch marks", "Scratch marks (finding)", "Scratch (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Scratch marks", "shortest_name_length": 7}
{"curie": "MONDO:0054838", "names": ["CMH27", "cardiomyopathy, FAMILIAL hypertrophic 27", "cardiomyopathy, familial hypertrophic 27", "CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC 27", "CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 27", "Familial Hypertrophic Cardiomyopathy Type 27"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiomyopathy, familial hypertrophic 27", "shortest_name_length": 5}
{"curie": "UMLS:C3272828", "names": ["Colon DLBCL", "Colon Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colon Diffuse Large B-Cell Lymphoma", "shortest_name_length": 11}
{"curie": "MONDO:0035432", "names": ["LGMD type R24", "POMGNT2-related LGMD R24", "POMGNT2-related muscular dystrophy", "limb-girdle muscular dystrophy type R24", "POMGNT2-related limb-girdle muscular dystrophy R24"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "POMGNT2-related limb-girdle muscular dystrophy R24", "shortest_name_length": 13}
{"curie": "MONDO:0001859", "names": ["algoneurodystrophy", "Algoneurodystrophy", "Algoneurodystrophy, unspecified site", "Algoneurodystrophy, site unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "algoneurodystrophy", "shortest_name_length": 18}
{"curie": "MONDO:0019810", "names": ["TEN", "TENS", "lyell", "Lyell", "lyells", "SJS-TEN", "LYELL SYNDROME", "Lyell Syndrome", "lyell syndrome", "Lyell syndrome", "Lyell's disease", "lyells syndrome", "LYELL'S SYNDROME", "SYNDROME LYELL'S", "lyell's syndrome", "Lyell's Syndrome", "Lyell's syndrome", "Syndrome, Lyell's", "Lyell's Syndromes", "Syndromes, Lyell's", "toxic epidermolysis", "Lyell syndrome (disorder)", "Toxic epidermal necrolysis", "Toxic Epidermal Necrolyses", "toxic epidermal necrolyses", "TOXIC EPIDERMAL NECROLYSIS", "toxic epidermal necrolysis", "EPIDERMOLYSIS, ACUTE TOXIC", "Toxic Epidermal Necrolysis", "Necrolysis, Toxic Epidermal", "necrolysis; toxic epidermal", "NECROLYSIS, TOXIC EPIDERMAL", "TOXIC EPIDEONEAL NECROLYSIS", "Necrolyses, Toxic Epidermal", "Epidermal Necrolysis, Toxic", "Epidermal Necrolyses, Toxic", "TEN (toxic epidermal necrolysis)", "TEN - Toxic epidermal necrolysis", "toxic epidermal necrolysis (TEN)", "Toxic epidermal necrolysis [Lyell]", "Toxic epidermal necrolysis (disorder)", "toxic epidermal necrolysis (diagnosis)", "Necrolysis epidermal toxic (Lyell type)", "Nonstaphylococcal Scalded Skin Syndrome", "Scalded Skin Syndrome, Nonstaphylococcal", "Lyell's toxic epidermal necrolysis, subepidermal type", "Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "toxic epidermal necrolysis", "shortest_name_length": 3}
{"curie": "MONDO:0013727", "names": ["RPL", "Rpl", "RPRGL", "Rprgl", "RPRGL1", "stillbirth, recurrent", "STILLBIRTH, RECURRENT", "miscarriage, recurrent", "MISCARRIAGE, RECURRENT", "embryonic loss, recurrent", "EMBRYONIC LOSS, RECURRENT", "ABORTION, SPONTANEOUS, RECURRENT", "abortion, spontaneous, recurrent", "fetal loss, recurrent, susceptibility to", "FETAL LOSS, RECURRENT, SUSCEPTIBILITY TO", "F5 pregnancy loss, recurrent, susceptibility", "pregnancy loss, recurrent, susceptibility to, 1", "PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 1", "pregnancy loss, recurrent, susceptibility to, type 1", "pregnancy loss, recurrent, susceptibility caused by mutation in F5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pregnancy loss, recurrent, susceptibility to, 1", "shortest_name_length": 3}
{"curie": "UMLS:C5418923", "names": ["Locally Advanced Glioblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Glioblastoma", "shortest_name_length": 29}
{"curie": "MONDO:0021588", "names": ["Eyelid SGC", "eyelid SGC", "Eyelid Sebaceous Gland Carcinoma", "eyelid sebaceous gland carcinoma", "sebaceous gland of eyelid carcinoma", "carcinoma of sebaceous gland of eyelid", "Sebaceous Gland Carcinoma of the Eyelid", "sebaceous gland carcinoma of the eyelid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eyelid sebaceous gland carcinoma", "shortest_name_length": 10}
{"curie": "UMLS:C4289791", "names": ["Chronic Eosinophilic Leukemia with FIP1L1-PDGFRA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic Eosinophilic Leukemia with FIP1L1-PDGFRA", "shortest_name_length": 48}
{"curie": "UMLS:C3899977", "names": ["BCLC Stage C Hepatocellular Cancer", "BCLC Stage C Hepatocellular Carcinoma", "Barcelona Clinic Liver Cancer Stage C Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "BCLC Stage C Hepatocellular Carcinoma", "shortest_name_length": 34}
{"curie": "UMLS:C0278725", "names": ["limited stage SCLC", "SCLC, limited stage", "oat cell lung cancer, limited stage", "Small cell lung cancer limited stage", "Limited Stage Small Cell Lung Cancer", "limited-stage small cell lung cancer", "limited stage small cell lung cancer", "small cell lung cancer, limited stage", "lung cancer, limited stage small cell", "Limited Stage Small Cell Lung Carcinoma", "Limited Stage Lung Small Cell Carcinoma", "Limited Stage Small Cell Carcinoma of Lung", "Limited Stage Small Cell Carcinoma of the Lung", "small cell carcinoma of lung with limited stage disease", "small cell carcinoma of lung with limited stage disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small cell lung cancer limited stage", "shortest_name_length": 18}
{"curie": "UMLS:C0334309", "names": ["Papillotubular adenocarcinoma", "Tubulopapillary adenocarcinoma", "Adenocarcinoma in tubolovillous adenoma", "adenocarcinoma in tubulovillous adenoma", "Adenocarcinoma in tubulovillous adenoma", "Adenocarcinoma in Tubulovillous Adenoma", "[M] Adenocarcinoma in tubulovillous adenoma", "adenocarcinoma in tubulovillous adenoma (diagnosis)", "Adenocarcinoma in tubulovillous adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma in tubulovillous adenoma", "shortest_name_length": 29}
{"curie": "MONDO:0022785", "names": ["cleft palate cardiac defect ectrodactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleft palate cardiac defect ectrodactyly", "shortest_name_length": 40}
{"curie": "MONDO:0005614", "names": ["PAASC", "Adenosquamous carcinoma", "Pancreatic Adenoacanthoma", "pancreatic adenoacanthoma", "Pancreatic Adenosquamous Cancer", "pancreatic adenosquamous cancer", "pancreas adenosquamous carcinoma", "adenosquamous pancreas carcinoma", "pancreatic adenosquamous carcinoma", "Pancreatic Adenosquamous Carcinoma", "Adenosquamous carcinoma of pancreas", "adenosquamous carcinoma of pancreas", "Pancreatic Mucoepidermoid Carcinoma", "Adenosquamous Carcinoma of Pancreas", "pancreatic mucoepidermoid carcinoma", "Adenosquamous Carcinoma of the Pancreas", "adenosquamous carcinoma of the pancreas", "pancreatic mixed squamous and adenocarcinoma", "Pancreatic Mixed Squamous and Adenocarcinoma", "adenosquamous carcinoma of pancreas (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic adenosquamous carcinoma", "shortest_name_length": 5}
{"curie": "UMLS:C4682656", "names": ["Stage I Gestational Trophoblastic Neoplasm AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Gestational Trophoblastic Neoplasm AJCC v8", "shortest_name_length": 50}
{"curie": "UMLS:C0852970", "names": ["Dacryoadenitis acquired"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dacryoadenitis acquired", "shortest_name_length": 23}
{"curie": "UMLS:C0392530", "names": ["Procidentia", "procidentia", "procidentias", "Procidentia uteri", "procidentia uteri", "Uterine procidentia", "uterine procidentia", "Procidentia (uteri) NOS", "Complete uterine prolapse", "uterine prolapse complete", "Uterine prolapse, complete", "uterus; prolapse, complete", "prolapse; uterus, complete", "Third Degree Uterine Prolapse", "third degree uterine prolapse", "Third degree uterine prolapse", "prolapse; uterus, third degree", "uterus; prolapse, third degree", "complete uterovaginal prolapse", "Complete uterovaginal prolapse", "Uterine prolapse, third degree", "Uterovaginal prolapse, complete", "UTEROVAGINAL PROLAPSE, COMPLETE", "uterovaginal; prolapse, complete", "prolapse; uterovaginal, complete", "complete uterine prolapse was observed", "Third degree uterine prolapse (disorder)", "third degree uterine prolapse (diagnosis)", "complete uterovaginal prolapse (diagnosis)", "uterine prolapse complete (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Third degree uterine prolapse", "shortest_name_length": 11}
{"curie": "MONDO:0030989", "names": ["SPGF53", "spermatogenic failure 53", "SPERMATOGENIC FAILURE 53"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 53", "shortest_name_length": 6}
{"curie": "MONDO:0035821", "names": ["isolated female hypospadias"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated female hypospadias", "shortest_name_length": 27}
{"curie": "MONDO:0018965", "names": ["Alport", "Alport Syndrome", "Alport syndrome", "alport syndrome", "syndrome alport", "ALPORT SYNDROME", "alports syndrome", "Syndrome, Alport", "Alport's Syndrome", "Alport's syndrome", "alport's syndrome", "Dickinson syndrome", "hereditary nephritis", "Hereditary Nephritis", "Alport syndrome (AS, ATS)", "Alport syndrome (disorder)", "Alport deafness-nephropathy", "deafness-nephritis syndrome", "Alport syndrome (diagnosis)", "hereditary hematuria syndrome", "hematuric hereditary nephritis", "hemorrhagic familial nephritis", "hematuric familial nephropathy", "Alport hearing loss-nephropathy", "hearing loss-nephritis syndrome", "congenital hereditary hematuria", "hemorrhagic hereditary nephritis", "NEPHROPATHY AND DEAFNESS, HEREDITARY", "HEREDITARY NEPHRITIS ALPORTS SYNDROME", "hereditary nephritis-deafness syndrome", "hereditary interstitial pyelonephritis", "Hematuria Nephropathy Deafness Syndrome", "Hematuria-Nephropathy-Deafness Syndrome", "HEREDITARY NEPHRITIS <ALPORTS SYNDROME>", "hematuria-nephropathy-deafness syndrome", "Syndrome, Hematuria-Nephropathy-Deafness", "NEPHRITIS WITH NERVE DEAFNESS, HEREDITARY", "hereditary familial congenital hemorrhagic nephritis", "hereditary nephritis-deafness-abnormal thrombogenesis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alport syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0006543", "names": ["DEB", "epidermolysis bullosa dystrophic", "Dystrophic epidermolysis bullosa", "bullosa dystrophic epidermolysis", "dystrophic epidermolysis bullosa", "Dermolytic epidermolysis bullosa", "Dystrophic Epidermolysis Bullosa", "dermolytic epidermolysis bullosa", "Epidermolysis bullosa, dystrophic", "bullosa dystrophica epidermolysis", "Bullosa, Dystrophic Epidermolysis", "Epidermolysis Bullosa Dystrophica", "Epidermolysis Bullosa, Dystrophic", "epidermolysis bullosa dystrophica", "epidermolysis bullosa, dermolytic", "Dystrophic Epidermolysis Bullosas", "Epidermolysis bullosa dystrophica", "Dystrophica, Epidermolysis Bullosa", "Epidermolysis Bullosas, Dystrophic", "Bullosa Dystrophica, Epidermolysis", "Bullosas, Dystrophic Epidermolysis", "Epidermolysis Bullosa Dystrophicas", "epidermolysis; bullosa, dystrophica", "Dystrophicas, Epidermolysis Bullosa", "Bullosa Dystrophicas, Epidermolysis", "DEB - Dystrophic epidermolysis bullosa", "Dystrophic epidermolysis bullosa (disorder)", "epidermolysis bullosa dystrophica (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolysis bullosa dystrophica", "shortest_name_length": 3}
{"curie": "UMLS:C5446513", "names": ["Conjunctival Follicular Lymphoma", "Primary Conjunctival Follicular Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conjunctival Follicular Lymphoma", "shortest_name_length": 32}
{"curie": "UMLS:C0278553", "names": ["COLON CANCER RECURRENT", "Recurrent Colon Cancer", "Colon cancer recurrent", "recurrent colon cancer", "colon cancer, recurrent", "Recurrent Colon Carcinoma", "Colon carcinoma recurrent", "Carcinoma colon recurrent", "Recurrent Cancer of Colon", "Recurrent Cancer of the Colon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colon cancer recurrent", "shortest_name_length": 22}
{"curie": "MONDO:0015646", "names": ["orgasm-induced seizures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orgasm-induced seizures", "shortest_name_length": 23}
{"curie": "UMLS:C0153886", "names": ["AML in Remission", "ANLL in Remission", "Acute Myeloid Leukemia in Remission", "Acute myeloid leukemia in remission", "Acute myeloid leukaemia in remission", "Acute myeloid leukemia, in remission", "Acute Myeloid Leukemia (in Remission)", "Acute myeloid leukemia (in remission)", "Acute myeloid leukaemia, in remission", "Acute myeloid leukaemia (in remission)", "Acute Myelocytic Leukemia in Remission", "acute myelogenous leukemia in remission", "Acute Myelogenous Leukemia in Remission", "Acute Myeloblastic Leukemia in Remission", "acute myeloblastic leukemia in remission", "Acute Granulocytic Leukemia in Remission", "Acute myeloblastic leukemia, in remission", "Acute Nonlymphocytic Leukemia in Remission", "Acute Non-Lymphocytic Leukemia in Remission", "Acute Nonlymphoblastic Leukemia in Remission", "acute myelogenous leukemia (AML) in remission", "Acute Non-Lymphoblastic Leukemia in Remission", "Acute myeloid leukemia in remission (disorder)", "acute myelogenous leukemia in remission (diagnosis)", "acute myeloblastic leukemia in remission (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute myeloid leukemia in remission", "shortest_name_length": 16}
{"curie": "MONDO:0021245", "names": ["Oral Tumor", "Oral tumor", "oral lesion", "tumor mouth", "mouth tumor", "lesion oral", "Mouth Tumor", "Oral lesion", "MOUTH TUMOR", "ORAL LESION", "Mouth tumor", "tumour mouth", "lesions oral", "mouth lesion", "MOUTH LESION", "mouth tumors", "Mouth--Tumors", "Oral neoplasm", "mouth tumours", "lesions mouth", "oral neoplasm", "Oral Neoplasm", "tumor of mouth", "Tumor of mouth", "NEOPLASM MOUTH", "mouth neoplasm", "Mouth Neoplasm", "Neoplasm, Oral", "Neoplasm mouth", "Mouth neoplasm", "oral neoplasms", "of mouth tumor", "Oral Neoplasms", "Mouth Neoplasms", "mouth neoplasms", "Tumour of mouth", "Neoplasms, Oral", "MOUTH NEOPLASIA", "Neoplasm, Mouth", "Mouth neoplasia", "Neoplasms, Mouth", "Oral neoplasm NOS", "neoplasm of mouth", "Oral Cavity Tumor", "oral cavity tumor", "Neoplasm of mouth", "cavity oral tumors", "Tumor of oral cavity", "Oral Cavity Neoplasm", "oral cavity neoplasm", "tumor of oral cavity", "mouth tumor or cancer", "Tumour of oral cavity", "Neoplasm of the mouth", "Lesion of oral cavity", "Oral lesion (disorder)", "Neoplasm of oral cavity", "neoplasm of oral cavity", "Lip and Oral Cavity Tumor", "Lip and Oral Cavity Tumour", "Neoplasm of the oral cavity", "Lip and Oral Cavity Neoplasm", "Neoplasm of mouth (disorder)", "neoplasm of mouth (diagnosis)", "oral cavity neoplasm (disease)", "Tumor of oral cavity (disorder)", "neoplasm of oral cavity (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oral cavity neoplasm", "shortest_name_length": 10}
{"curie": "UMLS:C1512252", "names": ["Grade 2 Endometrial Endometrioid Carcinoma", "Grade 2 Endometrial Endometrioid Adenocarcinoma", "FIGO Grade 2 Endometrial Endometrioid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Grade 2 Endometrial Endometrioid Adenocarcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0009824", "names": ["HP2", "Oxalosis 2", "Oxalosis II", "oxalosis II", "OXALOSIS II", "Oxalosis type II", "glyceric aciduria", "GLYCERIC ACIDURIA", "Glyceric aciduria", "L-glyceric aciduria", "type II hyperoxaluria", "GRHPR primary hyperoxaluria", "primary hyperoxaluria type 2", "Primary hyperoxaluria type 2", "primary hyperoxaluria type II", "Primary Hyperoxaluria Type II", "Primary hyperoxaluria type II", "Primary hyperoxaluria, type II", "hyperoxaluria, primary, type 2", "HYPEROXALURIA, PRIMARY, TYPE II", "hyperoxaluria, primary, type II", "Hyperoxaluria, Primary, Type II", "Glyoxylate reductase deficiency", "Glyceric dehydrogenase deficiency", "type II hyperoxaluria (diagnosis)", "Deficiency of glyoxylate reductase", "Glycerate dehydrogenase deficiency", "D-glycerate dehydrogenase deficiency", "D-GLYCERATE DEHYDROGENASE DEFICIENCY", "Deficiency of glycerate dehydrogenase", "Primary hyperoxaluria, type II (disorder)", "primary hyperoxaluria caused by mutation in GRHPR", "GLYOXYLATE REDUCTASE/HYDROXYPYRUVATE REDUCTASE DEFICIENCY", "Glyoxylate reductase-hydroxypyruvate reductase deficiency", "glyoxylate reductase/hydroxypyruvate reductase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary hyperoxaluria type 2", "shortest_name_length": 3}
{"curie": "UMLS:C5556905", "names": ["Primary Bone Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Bone Hodgkin Lymphoma", "shortest_name_length": 29}
{"curie": "MONDO:0060781", "names": ["Preeyasombat Varavithya syndrome", "Preeyasombat-Varavithya syndrome", "Fanconi syndrome caused by degraded tetracycline"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Preeyasombat-Varavithya syndrome", "shortest_name_length": 32}
{"curie": "UMLS:C3163829", "names": ["Sepsis due to Gram negative bacteria", "Sepsis caused by Gram negative bacteria", "Sepsis caused by Gram negative bacteria (disorder)", "Severe sepsis with acute organ dysfunction caused by Gram-negative bacteria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sepsis caused by Gram negative bacteria", "shortest_name_length": 36}
{"curie": "MONDO:0018365", "names": ["ovarian non-epithelial cancer", "non-epithelial cancer of ovary", "ovarian malignant non-epithelial tumor", "malignant non-epithelial tumor of ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant non-epithelial tumor of ovary", "shortest_name_length": 29}
{"curie": "MONDO:0030918", "names": ["MRD52", "autosomal dominant mental retardation 52", "mental retardation, autosomal dominant 52", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 52", "autosomal dominant intellectual disability 52", "intellectual disability, autosomal dominant 52", "autosomal dominant intellectual developmental disorder 52", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 52"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 52", "shortest_name_length": 5}
{"curie": "MONDO:0015950", "names": ["genetic skin tumor", "inherited skin tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited skin tumor", "shortest_name_length": 18}
{"curie": "MONDO:0018088", "names": ["FMF", "fmf", "Periodic Disease", "Periodic disease", "armenian disease", "ARMENIAN DISEASE", "periodic disease", "Disease, Periodic", "Periodic diseases", "periodic diseases", "Periodic Diseases", "Diseases, Periodic", "Periodic peritonitis", "Periodic Peritonitis", "peritonitis; periodic", "PERITONITIS, PERIODIC", "Peritonitis, Periodic", "periodic; peritonitis", "Wolff Periodic Disease", "PERIODIC POLYSEROSITIS", "Periodic polyserositis", "Periodic Peritonitides", "periodic; polyserositis", "Recurrent Polyserositis", "polyserositis; periodic", "recurrent polyserositis", "Wolffs Periodic Disease", "Recurrent polyserositis", "Peritonitides, Periodic", "Periodic Disease, Wolff", "Disease, Wolff Periodic", "REIMANN PERIODIC DISEASE", "Polyserositis, Recurrent", "POLYSEROSITIS, RECURRENT", "Wolff's Periodic Disease", "Periodic Disease, Wolffs", "Paroxysmal polyserositis", "Disease, Wolff's Periodic", "Periodic Disease, Wolff's", "Recurrent Polyserositides", "Polyserositides, Recurrent", "SIEGAL-CATTAN-MAMOU DISEASE", "Familial Mediterranean fever", "familial mediterranean fever", "Familial mediterranean fever", "familial Mediterranean fever", "mediterranean fever familial", "mediterranean familial fever", "Familial Mediterranean Fever", "FAMILIAL MEDITERRANEAN FEVER", "Benign paroxysmal peritonitis", "Periodic familial peritonitis", "Mediterranean Fever, Familial", "MEDITERRANEAN FEVER, FAMILIAL", "Benign Paroxysmal Peritonitis", "benign paroxysmal peritonitis", "fever; mediterranean, familial", "Paroxysmal Peritonitis, Benign", "Peritonitis, Benign Paroxysmal", "Benign recurrent polyserositis", "mediterranean; fever, familial", "benign recurrent polyserositis", "Benign Paroxysmal Peritonitides", "Familial recurrent polyserositis", "Paroxysmal Peritonitides, Benign", "Peritonitides, Benign Paroxysmal", "familial paroxysmal polyserositis", "Familial paroxysmal polyserositis", "Familial Paroxysmal Polyserositis", "Paroxysmal Polyserositis, Familial", "FMF - Familial Mediterranean fever", "Polyserositis, Familial Paroxysmal", "POLYSEROSITIS, FAMILIAL PAROXYSMAL", "MEF - Familial Mediterranean fever", "Familial Paroxysmal Polyserositides", "Paroxysmal Polyserositides, Familial", "Polyserositides, Familial Paroxysmal", "Familial Mediterranean fever (disorder)", "familial Mediterranean fever (diagnosis)", "familial Mediterranean fever with recurrent polyserositis", "familial Mediterranean fever with recurrent polyserositis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial Mediterranean fever", "shortest_name_length": 3}
{"curie": "MONDO:0009397", "names": ["NSPH", "NHPT", "Nsph", "NSHPT", "hyperparathyroidism, neonatal", "neonatal severe hyperparathyroidism", "HYPERPARATHYROIDISM, NEONATAL SEVERE", "hyperparathyroidism, neonatal severe", "Neonatal severe primary hyperparathyroidism", "Neonatal Severe Primary Hyperparathyroidism", "neonatal severe primary hyperparathyroidism", "Hyperparathyroidism, Neonatal Severe Primary", "hyperparathyroidism, neonatal severe primary", "HYPERPARATHYROIDISM, NEONATAL SEVERE PRIMARY", "Neonatal severe primary hyperparathyroidism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal severe primary hyperparathyroidism", "shortest_name_length": 4}
{"curie": "UMLS:C4288773", "names": ["Malignant Vulvar Phyllodes Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Vulvar Phyllodes Tumor", "shortest_name_length": 32}
{"curie": "MONDO:0004021", "names": ["mediastinum lymphoma", "mediastinal lymphoma", "Mediastinal Lymphoma", "Lymphoma of Mediastinum", "Lymphoma of mediastinum", "lymphoma of mediastinum", "Lymphoma of the Mediastinum", "lymphoma of the mediastinum", "primary mediastinal lymphoma", "Primary Mediastinal Lymphoma", "Mediastinal Malignant Lymphoma", "mediastinal malignant lymphoma", "malignant lymphoma of mediastinum", "malignant lymphoma of mediastinum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mediastinal malignant lymphoma", "shortest_name_length": 20}
{"curie": "MONDO:0020686", "names": ["Acute tonsillitis", "acute adenoiditis", "acute tonsillitis", "Acute Tonsillitis", "Tonsillitis acute", "Tonsillitis;acute", "TONSILLITIS, ACUTE", "Infective tonsillitis", "Tonsillitis acute NOS", "infective tonsillitis", "Tonsillitis, infective", "Acute tonsillitis, NOS", "Tonsillitis (acute) NOS", "Acute tonsillitis (disorder)", "acute tonsillitis (diagnosis)", "Acute tonsillitis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute tonsillitis", "shortest_name_length": 17}
{"curie": "MONDO:0014644", "names": ["SPG74", "hereditary spastic paraplegia 74", "IBA57 hereditary spastic paraplegia", "hereditary spastic paraplegia type 74", "autosomal recessive spastic paraplegia 74", "SPASTIC PARAPLEGIA 74, AUTOSOMAL RECESSIVE", "spastic paraplegia 74, autosomal recessive", "autosomal recessive spastic paraplegia type 74", "Autosomal recessive spastic paraplegia type 74", "hereditary spastic paraplegia caused by mutation in IBA57", "Autosomal recessive spastic paraplegia type 74 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 74", "shortest_name_length": 5}
{"curie": "UMLS:C1710396", "names": ["Thymic Atypical Carcinoid Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thymic Atypical Carcinoid Tumor", "shortest_name_length": 31}
{"curie": "MONDO:0000551", "names": ["retroperitoneal neuroblastoma", "retroperitoneal space neuroblastoma", "neuroblastoma of retroperitoneal space"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retroperitoneal neuroblastoma", "shortest_name_length": 29}
{"curie": "MONDO:0016696", "names": ["Oligodendroglioma malignant", "Malignant oligodendroglioma", "Malignant Oligodendroglioma", "malignant oligodendroglioma", "Anaplastic Oligodendroglioma", "oligodendroglioma, malignant", "Anaplastic oligodendroglioma", "anaplastic oligodendroglioma", "Oligodendroglioma, Malignant", "Oligodendroglioma, Anaplastic", "Oligodendroglioma, anaplastic", "anaplastic oligodendrogliomas", "Anaplastic Oligodendrogliomas", "Oligodendrogliomas, Anaplastic", "Anaplastic Oligodendroglioma, NOS", "undifferentiated oligodendroglioma", "Oligodendroglioma, anaplastic type", "Undifferentiated Oligodendroglioma", "WHO Grade 3 Oligodendroglial Tumor", "WHO Grade III Oligodendroglial Tumor", "WHO grade III oligodendroglial tumor", "WHO Grade 3 Oligodendroglial Neoplasm", "WHO grade III oligodendroglial neoplasm", "WHO Grade III Oligodendroglial Neoplasm", "malignant oligodendroglioma (diagnosis)", "CNS neoplasm malignant oligodendroglioma", "oligodendroglioma, anaplastic, malignant", "Anaplastic Oligodendroglioma, Not Otherwise Specified", "Oligodendroglioma, anaplastic (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anaplastic oligodendroglioma", "shortest_name_length": 27}
{"curie": "UMLS:C3542500", "names": ["Diabetes Insipidus Renalis", "ADH-Resistant Diabetes Insipidus", "Vasopressin-Resistant Diabetes Insipidus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ADH-Resistant Diabetes Insipidus", "shortest_name_length": 26}
{"curie": "MONDO:0004351", "names": ["iol", "IOL", "PIOL", "Ocular lymphoma", "intraocular lymphoma", "Intraocular Lymphoma", "Intraocular lymphoma", "Lymphoma, Intraocular", "lymphoma, intraocular", "Intraocular Lymphomas", "Vitreoretinal lymphoma", "Lymphomas, Intraocular", "intraocular lymphoma (IOL)", "primary intraocular lymphoma", "Primary Intraocular Lymphoma", "Primary intraocular lymphoma", "intraocular non-Hodgkin's lymphoma", "Primary Intraocular Non-Hodgkin Lymphoma", "Primary intraocular non-Hodgkin lymphoma", "Intraocular non-Hodgkin malignant lymphoma", "primary intraocular non-Hodgkin's lymphoma", "Primary CNS lymphoma with ocular involvement", "intraocular non-Hodgkin's lymphoma (diagnosis)", "Primary intraocular non-Hodgkin malignant lymphoma", "Intraocular non-Hodgkin malignant lymphoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intraocular lymphoma", "shortest_name_length": 3}
{"curie": "MONDO:0013453", "names": ["LCA8", "LEBER CONGENITAL AMAUROSIS 8", "Leber congenital amaurosis 8", "CRB1 Leber congenital amaurosis", "Leber congenital amaurosis type 8", "Leber congenital amaurosis caused by mutation in CRB1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leber congenital amaurosis 8", "shortest_name_length": 4}
{"curie": "MONDO:0017437", "names": ["agenesis; arm", "arm; agenesis", "Amelia of the arm", "upper limb; amelia", "amelia; upper limb", "agenesis; upper limb", "upper limb; agenesis", "amelia of upper limb", "Amelia of upper limb", "limb; agenesis, upper", "agenesis; limb, upper", "amelia of an upper limb", "forelimb non-syndromic amelia", "Congenital absence of upper limb", "absence; limb, congenital, upper", "limb; absence, congenital, upper", "amelia of upper limb (diagnosis)", "non-syndromic amelia of forelimb", "congenital absence of upper limb", "congenital deformity absence upper limb", "Congenital complete absence of upper limb", "Congenital absence of upper limb, complete", "Congenital absence of upper limb (disorder)", "Transverse deficiency of arm, shoulder level", "Congenital complete absence of upper limb(s)", "congenital absence of upper limb (diagnosis)", "congenital deformity absence upper limb complete", "Congenital complete absence of upper limb (disorder)", "Congenital complete absence of upper limb (diagnosis)", "Congenital complete absence of unspecified upper limb"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amelia of upper limb", "shortest_name_length": 13}
{"curie": "MONDO:0004519", "names": ["Synovial Angioma", "synovial angioma", "angioma of synovium", "Synovial Hemangioma", "synovial hemangioma", "Angioma of Synovium", "hemangioma of Synovium", "Hemangioma of Synovium", "hemangioma of synovium", "Angioma of the Synovium", "angioma of the synovium", "hemangioma of the synovium", "Hemangioma of the Synovium", "layer of synovial tissue hemangioma", "hemangioma of layer of synovial tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "synovial angioma", "shortest_name_length": 16}
{"curie": "UMLS:C1378463", "names": ["Relapsed Hypopharynx Carcinoma", "Relapsed Cancer of Hypopharynx", "Relapsed Hypopharyngeal Cancer", "Recurrent Hypopharynx Carcinoma", "Recurrent Hypopharyngeal Cancer", "Recurrent Cancer of Hypopharynx", "Relapsed Carcinoma of Hypopharynx", "Relapsed Hypopharyngeal Carcinoma", "Recurrent Carcinoma of Hypopharynx", "Relapsed Cancer of the Hypopharynx", "Recurrent Hypopharyngeal Carcinoma", "Recurrent Cancer of the Hypopharynx", "Relapsed Carcinoma of the Hypopharynx", "Recurrent Carcinoma of the Hypopharynx", "Recurrent Hypopharyngeal Throat Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Relapsed Hypopharynx Carcinoma", "shortest_name_length": 30}
{"curie": "UMLS:C0393574", "names": ["Late onset Huntington disease", "Late Onset Huntington Disease", "Huntington disease late onset", "Late-Onset Huntington Disease", "Huntington Disease, Late Onset", "Huntington Disease, Late-Onset", "Late onset Huntington's disease", "Late onset Huntington's disease (disorder)", "Late onset Huntington's disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Huntington Disease, Late Onset", "shortest_name_length": 29}
{"curie": "UMLS:C4763832", "names": ["Metastatic Kidney Medullary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Kidney Medullary Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0002991", "names": ["Adenocarcinofibroma", "adenocarcinofibroma", "Malignant Adenofibroma", "malignant adenofibroma", "adenofibroma, malignant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenocarcinofibroma", "shortest_name_length": 19}
{"curie": "UMLS:C0520594", "names": ["microcalcification", "Microcalcification", "microcalcification breast", "breast microcalcification", "Breast microcalcification", "Breast Microcalcification", "breast microcalcifications", "breasts microcalcification", "microcalcifications breast", "Microcalcifications of the breast", "Microcalcifications of the breast (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Microcalcification", "shortest_name_length": 18}
{"curie": "MONDO:0000637", "names": ["skeletal system cancer", "musculoskeletal system cancer", "cancer of musculoskeletal system", "malignant musculoskeletal system neoplasm", "malignant neoplasm of musculoskeletal system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "musculoskeletal system cancer", "shortest_name_length": 22}
{"curie": "MONDO:0100115", "names": ["AFM", "AFM syndrome", "Acute flaccid myelitis", "myelitis acute flaccid", "acute flaccid myelitis", "Acute Flaccid Myelitis", "Acute flaccid myelitis (disorder)", "Acute flaccid myelitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute flaccid myelitis", "shortest_name_length": 3}
{"curie": "UMLS:C1710165", "names": ["Sporadic Gastric Diffuse Adenocarcinoma", "Sporadic Diffuse Gastric Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sporadic Gastric Diffuse Adenocarcinoma", "shortest_name_length": 39}
{"curie": "MONDO:0054588", "names": ["NSLH2", "NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2", "Noonan Syndrome-Like Disorder with Loose Anagen Hair 2", "Noonan syndrome-like disorder with loose anagen hair 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Noonan syndrome-like disorder with loose anagen hair 2", "shortest_name_length": 5}
{"curie": "MONDO:0008795", "names": ["GLSP", "Gillespie syndrome", "GILLESPIE SYNDROME", "gillespie syndrome", "GILLESPIE syndrome", "Gillespie syndrome (disorder)", "Gillespie syndrome (diagnosis)", "Aniridia cerebellar ataxia mental deficiency", "Aniridia, partial-cerebellar ataxia-oligophrenia", "aniridia, cerebellar ataxia and mental deficiency", "Aniridia, Cerebellar Ataxia, And Mental Deficiency", "ANIRIDIA, CEREBELLAR ATAXIA, AND MENTAL RETARDATION", "aniridia, cerebellar ataxia, and mental retardation", "Aniridia, partial-cerebellar ataxia-mental retardation", "aniridia, cerebellar ataxia, and intellectual disability", "Aniridia-cerebellar ataxia-intellectual disability syndrome", "aniridia-cerebellar ataxia-intellectual disability syndrome", "Aniridia, cerebellar ataxia, intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aniridia-cerebellar ataxia-intellectual disability syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0020497", "names": ["Turcot syndrome with polyposis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Turcot syndrome with polyposis", "shortest_name_length": 30}
{"curie": "MONDO:0003692", "names": ["Malignant Mesenchymoma", "malignant mesenchymoma", "adult malignant mesenchymoma", "Adult Malignant Mesenchymoma", "malignant mesenchymoma, adult", "mesenchymoma, malignant, adult", "malignant mesenchymoma of adults"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult malignant mesenchymoma", "shortest_name_length": 22}
{"curie": "MONDO:0035823", "names": ["KLHL7-related BOS-like syndrome", "KLHL7-related Bohring-Opitz-like syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "KLHL7-related Bohring-Opitz-like syndrome", "shortest_name_length": 31}
{"curie": "UMLS:C4761157", "names": ["Laryngeal Chondrosarcoma", "Laryngeal chondrosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laryngeal chondrosarcoma", "shortest_name_length": 24}
{"curie": "UMLS:C0280315", "names": ["Posterior Tongue SCC", "SCC of Posterior Tongue", "SCC of the Posterior Tongue", "Posterior Tongue Squamous Cell Carcinoma", "Squamous Cell Carcinoma of Posterior Tongue", "Squamous Cell Carcinoma of the Posterior Tongue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Posterior Tongue Squamous Cell Carcinoma", "shortest_name_length": 20}
{"curie": "UMLS:C2826781", "names": ["Cellular Pleomorphic Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cellular Pleomorphic Adenoma", "shortest_name_length": 28}
{"curie": "MONDO:0032902", "names": ["JBTS36", "JOUBERT SYNDROME 36", "Joubert syndrome 36"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome 36", "shortest_name_length": 6}
{"curie": "UMLS:C0155556", "names": ["Acute Rheumatic Endocarditis", "acute rheumatic endocarditis", "Acute rheumatic endocarditis", "Rheumatic endocarditis, acute", "Acute rheumatic fever with endocarditis", "acute rheumatic endocarditis (diagnosis)", "Active rheumatic fever with endocarditis", "Acute rheumatic fever with endocarditis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute rheumatic endocarditis", "shortest_name_length": 28}
{"curie": "UMLS:C2697636", "names": ["Hyperdiploid ALL", "Hyperdiploid Acute Lymphoblastic Leukemia", "Hyperdiploid B Acute Lymphoblastic Leukemia", "Hyperdiploid B-Acute Lymphoblastic Leukemia", "Hyperdiploid B-Cell Acute Lymphoblastic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyperdiploid B Acute Lymphoblastic Leukemia", "shortest_name_length": 16}
{"curie": "UMLS:C1697250", "names": ["Testicular Perforation", "Testicular perforation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular perforation", "shortest_name_length": 22}
{"curie": "MONDO:0019988", "names": ["pauci-immune glomerulonephritis with ANCA", "pauci-immune glomerulonephritis with antineutrophil cytoplasmic antibody"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pauci-immune glomerulonephritis with ANCA", "shortest_name_length": 41}
{"curie": "MONDO:0005075", "names": ["TPC", "PTC", "PACT", "cancer papillary thyroid", "papillary thyroid cancer", "thyroid cancer papillary", "papillary cancer thyroid", "THYROID CANCER PAPILLARY", "thyroid papillary cancer", "Papillary thyroid cancer", "Papillary Thyroid Cancer", "Thyroid Cancer, Papillary", "thyroid cancer, papillary", "Thyroid cancer, papillary", "Cancer, Papillary Thyroid", "Papillary Thyroid Cancers", "Thyroid Cancers, Papillary", "Cancers, Papillary Thyroid", "carcinoma papillary thyroid", "Carcinoma papillary thyroid", "Papillary Cancer of Thyroid", "Thyroid papillary carcinoma", "papillary thyroid carcinoma", "Thyroid Papillary Carcinoma", "thyroid papillary carcinoma", "papillary carcinoma thyroid", "Papillary Thyroid Carcinoma", "CARCINOMA PAPILLARY THYROID", "THYROID PAPILLARY CARCINOMA", "papillary cancer of thyroid", "Papillary thyroid carcinoma", "Papillary Thyroid Carcinomas", "Thyroid Carcinoma, Papillary", "Carcinoma, Papillary Thyroid", "Carcinomas, Papillary Thyroid", "Thyroid Carcinomas, Papillary", "THYROID, CARCINOMA, PAPILLARY", "papillary carcinoma of thyroid", "PAPILLARY CARCINOMA OF THYROID", "Thyroid Gland Papillary Cancer", "Papillary Carcinoma of Thyroid", "Papillary Carcinoma Of Thyroid", "Papillary carcinoma of thyroid", "thyroid gland papillary cancer", "papillary cancer of the thyroid", "Papillary Cancer of the Thyroid", "Papillary Thyroid Carcinoma, NOS", "PTC - Papillary thyroid carcinoma", "Thyroid Gland Papillary Carcinoma", "thyroid gland papillary carcinoma", "Papillary Thyroid Gland Carcinoma", "PTC - papillary thyroid carcinoma", "papillary cancer of thyroid gland", "papillary thyroid gland carcinoma", "Papillary Cancer of Thyroid Gland", "Papillary Carcinoma of the Thyroid", "papillary carcinoma of the thyroid", "THYROID CANCER, PAPILLARY CARCINOMA", "Papillary Carcinoma of Thyroid Gland", "papillary carcinoma of thyroid gland", "Papillary Cancer of the Thyroid Gland", "papillary cancer of the thyroid gland", "Papillary thyroid carcinoma (disorder)", "Papillary Carcinoma of the Thyroid Gland", "papillary carcinoma of the thyroid gland", "Papillary carcinoma of the Thyroid gland", "papillary carcinoma of the thyroid gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid gland papillary carcinoma", "shortest_name_length": 3}
{"curie": "UMLS:C0410919", "names": ["fetal bradycardia", "Bradycardia Fetal", "Fetal bradycardia", "Bradycardia fetal", "Fetal Bradycardia", "Foetal bradycardia", "foetal bradycardia", "Bradycardia foetal", "Baseline Fetal Bradycardia", "Fetal bradycardia (disorder)", "fetal bradycardia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fetal bradycardia", "shortest_name_length": 17}
{"curie": "UMLS:C1332674", "names": ["AIDS-Related Anal Non-Hodgkin Lymphoma", "AIDS-Related Anal Non-Hodgkin's Lymphoma", "AIDS-Related Primary Anal Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Anal Non-Hodgkin Lymphoma", "shortest_name_length": 38}
{"curie": "MONDO:0020605", "names": ["X-linked recessive disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked recessive disease", "shortest_name_length": 26}
{"curie": "UMLS:C0862953", "names": ["Unresectable Cholangiocarcinoma", "Cholangiocarcinoma non-resectable", "Non-Resectable Cholangiocarcinoma", "Non-Resectable Cholangiocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cholangiocarcinoma non-resectable", "shortest_name_length": 31}
{"curie": "MONDO:0009990", "names": ["DKCA5", "Revesz syndrome", "REVESZ SYNDROME", "Revesz Syndrome", "Revesz-DeBuse syndrome", "Revesz Debuse syndrome", "Revesz DeBuse syndrome", "REVESZ SYNDROME (disorder)", "Revesz syndrome (disorder)", "DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 5", "dyskeratosis congenita, autosomal dominant 5", "Dyskeratosis Congenita, Autosomal Dominant 5", "Dyskeratosis Congenita, Autosomal Dominant, 5", "exudative retinopathy with bone marrow failure", "EXUDATIVE RETINOPATHY WITH BONE MARROW FAILURE", "Exudative retinopathy with bone marrow failure", "Exudative Retinopathy with Bone Marrow Failure", "dyskeratosis congenita with bilateral exudative retinopathy", "Dyskeratosis congenita with bilateral exudative retinopathy", "retinopathy-anemia-central nervous system anomalies syndrome", "Retinopathy-anemia-central nervous system anomalies syndrome", "Retinopathy, anemia, central nervous system anomalies syndrome", "Retinopathy, anaemia, central nervous system anomalies syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Revesz syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0017651", "names": ["primary myoclonus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary myoclonus", "shortest_name_length": 17}
{"curie": "UMLS:C0494930", "names": ["Unequal limb length", "Unequal Limb Length", "unequal length of limbs", "Unequal limb length (acquired)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unequal Limb Length", "shortest_name_length": 19}
{"curie": "MONDO:0007729", "names": ["DDH1", "acetabular dysplasia", "hip dysplasia, congenital", "hip dysplasia, developmental", "developmental dysplasia of the hip 1", "DEVELOPMENTAL DYSPLASIA OF THE HIP 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental dysplasia of the hip 1", "shortest_name_length": 4}
{"curie": "MONDO:0003699", "names": ["phobia", "Phobia", "PHOBIA", "PHOBIAS", "Phobias", "Phobia NOS", "Phobia, NOS", "Phobic state", "phobic state", "phobic; state", "state; phobia", "Abnormal fear", "abnormal fear", "state; phobic", "phobia; state", "Phobic anxiety", "phobic disorder", "PHOBIC DISORDER", "Phobic Neurosis", "Phobic disorder", "Phobic Disorder", "PHOBIC NEUROSIS", "phobic neurosis", "Phobic neurosis", "Phobic Neuroses", "neurosis; phobic", "Neuroses, Phobic", "Phobic disorders", "Disorder, Phobic", "Phobic Disorders", "Phobia (finding)", "phobic; neurosis", "Phobic state NOS", "phobic disorders", "Neurosis, phobic", "phobia (diagnosis)", "Phobia, unspecified", "Phobic anxiety disorder", "Phobic anxiety disorders", "anxiety disorder; phobic", "phobic; anxiety disorder", "Phobic disorder (disorder)", "Phobic anxiety disorder, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phobic disorder", "shortest_name_length": 6}
{"curie": "UMLS:C5421293", "names": ["Sinonasal Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Lymphoma", "shortest_name_length": 18}
{"curie": "UMLS:C1535888", "names": ["Sleep disorder due to a general medical condition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sleep disorder due to a general medical condition", "shortest_name_length": 49}
{"curie": "MONDO:0005855", "names": ["WATER WART", "water wart", "warts water", "mollusca contagiosa", "Mollusca contagiosa", "Molluscum contagious", "Molluscum verrucosum", "mollusca contagiosum", "Mollusca contagiosum", "molluscum contagious", "Molluscum contagiosum", "molluscum contagiosum", "MOLLUSCUM EPITHELIALE", "MOLLUSCUM CONTAGIOSUM", "contagiosum molluscum", "Molluscum Contagiosum", "MC - Molluscum contagiosum", "Molluscum contagiosum infection", "molluscum contagiosum (diagnosis)", "Molluscum contagiosum virus infection", "Molluscum Contagiosum Virus Infection", "Molluscum contagiosum viral infections", "Infection caused by Molluscum contagiosum", "Infection caused by Molluscum contagiosum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "molluscum contagiosum", "shortest_name_length": 10}
{"curie": "UMLS:C4525306", "names": ["Stage IVA Gallbladder Cancer", "Stage IVA Gallbladder Cancer AJCC v8", "Stage IVA Gallbladder Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Gallbladder Cancer AJCC v8", "shortest_name_length": 28}
{"curie": "UMLS:C5419580", "names": ["Allergy, Ant", "Ant Bite Allergy", "Ant Sting Allergy", "Venomous Ant Bite Allergy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Venomous Ant Bite Allergy", "shortest_name_length": 12}
{"curie": "MONDO:0003544", "names": ["spine cancer", "spinal cancer", "Spine--Cancer", "spinal neoplasm", "Intraspinal tumor", "intraspinal tumor", "spinal cord cancer", "spinal cord neoplasm", "cancer of spinal cord", "tumor of the spinal cord", "tumor of the Spinal Cord", "Neoplasm malig;spinal cord", "Malignant Spinal Cord Tumor", "malignant spinal cord tumor", "Malignant tumor of spinal cord", "malignant spinal cord neoplasm", "malignant tumor of spinal cord", "Malignant Spinal Cord Neoplasm", "Malignant Tumor of Spinal Cord", "Malignant tumour of spinal cord", "Spinal Cord Neoplasms, Malignant", "Malignant neoplasm of spinal cord", "malignant neoplasm of spinal cord", "Malignant Neoplasm of Spinal Cord", "malignant tumor of the Spinal Cord", "malignant tumor of the spinal cord", "Malignant spinal cord neoplasm NOS", "Malignant Tumor of the Spinal Cord", "Malignant Neoplasm of the Spinal Cord", "malignant neoplasm of the spinal cord", "malignant neosplasm of the spinal cord", "malignant spinal cord tumor (diagnosis)", "Malignant tumor of spinal cord (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal cord cancer", "shortest_name_length": 12}
{"curie": "MONDO:0009649", "names": ["MYMY", "MYMY1", "Moyamoya disease", "MOYAMOYA DISEASE", "MOYAMOYA DISEASE 1", "moyamoya disease 1", "Moyamoya disease 1", "spontaneous occlusion of the circle of Willis", "SPONTANEOUS OCCLUSION OF THE CIRCLE OF WILLIS", "Spontaneous occlusion of the circle of Willis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "moyamoya disease 1", "shortest_name_length": 4}
{"curie": "MONDO:0018178", "names": ["Intestinal Lymphangiectasis", "Intestinal Lymphangiectases", "Intestinal lymphangiectasia", "intestinal lymphangiectasia", "Lymphangiectasia intestinal", "Intestinal lymphangiectasis", "intestinal lymphangiectasis", "LYMPHANGIECTASIA, INTESTINAL", "Lymphangiectases, Intestinal", "Lymphangiectasia, Intestinal", "Lymphangiectasis, Intestinal", "Intestinal lymphangiectasia syndrome", "intestinal lymphangiectasia (disease)", "Intestinal lymphangiectasia (disorder)", "Intestinal lymphangiectasis (disorder)", "intestinal lymphangiectasia (diagnosis)", "Hypercatabolic protein-losing enteropathy", "ENTEROPATHY, HYPERCATABOLIC PROTEIN LOSING", "ENTEROPATHY, LYMPHANGIECTATIC PROTEIN-LOSING", "LYMPHEDEMA, NEONATAL, DUE TO EXUDATIVE ENTEROPATHY", "HYPOPROTEINEMIA, FAMILIAL, WITH LYMPHANGIECTATIC ENTEROPATHY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intestinal lymphangiectasia", "shortest_name_length": 27}
{"curie": "UMLS:C0280626", "names": ["stage III uterine sarcoma", "Stage III Uterine Sarcoma", "uterine sarcoma, stage III", "Stage III Uterine Sarcoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Uterine Sarcoma AJCC v7", "shortest_name_length": 25}
{"curie": "MONDO:0018908", "names": ["NHL", "nhl", "NHL, NOS", "nonhodgkin lymphoma", "Nonhodgkins Lymphoma", "Non Hodgkin Lymphoma", "NONHODGKINS LYMPHOMA", "NON-HODGKIN LYMPHOMA", "Non-Hodgkin lymphoma", "non-hodgkin lymphoma", "non-Hodgkin lymphoma", "Non-Hodgkin Lymphoma", "LYMPHOMA NON HODGKIN", "nonhodgkins lymphoma", "non hodgkin lymphoma", "Lymphoma, Nonhodgkin", "non-Hodgkins lymphoma", "NON HODGKINS LYMPHOMA", "nonhodgkin's lymphoma", "Lymphoma, Non-Hodgkin", "Non-Hodgkins Lymphoma", "Non-Hodgkins lymphoma", "non-hodgkins lymphoma", "LYMPHOMA, NON HODGKIN", "nonHodgkin's lymphoma", "Lymphoma;non Hodgkins", "non hodgkins lymphoma", "Lymphoma, Non Hodgkin", "Lymphoma, Nonhodgkins", "Nonhodgkin's Lymphoma", "Non-Hodgkin's lymphoma", "non-hodgkin's lymphoma", "non hodgkin's lymphoma", "Lymphoma, Non-Hodgkins", "NON-HODGKIN'S LYMPHOMA", "Non Hodgkin's Lymphoma", "Lymphoma, Non Hodgkins", "Non-Hodgkin`s lymphoma", "non-Hodgkin's lymphoma", "Non-Hodgkin's Lymphoma", "Lymphoma, Nonhodgkin's", "lymphoma, non-Hodgkin's", "non-Hodgkin's; lymphoma", "Lymphoma, Non-Hodgkin's", "lymphoma; non-Hodgkin's", "Lymphoma, Non Hodgkin's", "Non-Hodgkin lymphoma NOS", "Lymphoma (non-Hodgkin's)", "Non-Hodgkin lymphoma, NOS", "Non-Hodgkin's lymphoma NOS", "Diffuse malignant lymphoma", "Non-Hodgkin's lymphoma, NOS", "non hodgkin's lymphoma (NHL)", "non-Hodgkin's lymphoma (NHL)", "NHL - Non-Hodgkin's lymphoma", "Non-Hodgkin's Lymphoma (NHL)", "Non-Hodgkin malignant lymphoma", "Malignant lymphoma, non-Hodgkin", "Non-Hodgkin's malignant lymphoma", "Non-Hodgkin's lymphoma (disorder)", "Non-Hodgkin's lymphoma (clinical)", "Non-Hodgkin's lymphoma - disorder", "Malignant lymphoma, non-Hodgkin's", "non-Hodgkin's lymphoma (diagnosis)", "Diffuse Small Cleaved Cell Lymphoma", "Diffuse Small Cleaved-Cell Lymphoma", "Small Cleaved-Cell Lymphoma, Diffuse", "Small Cleaved Cell Lymphoma, Diffuse", "MALIGNANT LYMPHOMA NON HODGKINS TYPE", "Lymphoma, Small Cleaved Cell, Diffuse", "Malignant lymphoma, cleaved cell, NOS", "Lymphoma, Small Cleaved-Cell, Diffuse", "Malignant lymphoma, non-Hodgkin's NOS", "Malignant lymphoma, non-Hodgkin's, NOS", "diffuse; lymphoma, small cell, cleaved", "lymphoma; diffuse, small cell, cleaved", "Malignant lymphoma, non-Hodgkin's type", "malignant lymphoma, small cleaved cell", "lymphoma; small cell, cleaved (diffuse)", "small cell; lymphoma, cleaved (diffuse)", "Malignant lymphoma - small cleaved cell", "Non-Hodgkin's lymphoma, unspecified type", "Lymphoma, Atypical Diffuse Small Lymphoid", "Malignant lymphoma, small cleaved cell, NOS", "Lymphocytic lymphoma, poorly differentiated", "Non-Hodgkin lymphoma (morphologic abnormality)", "Malignant lymphoma, small cleaved cell, diffuse", "Malignant lymphoma, diffuse, small cleaved cell", "Malignant lymphoma - small cleaved cell (disorder)", "malignant lymphoma, small cleaved cell (diagnosis)", "Small cleaved cell (diffuse) non-Hodgkin's lymphoma", "Malignant lymphoma, lymphocytic, poorly differentiated", "Malignant lymphoma, lymphocytic - poorly differentiated", "Diffuse non-Hodgkin's small cleaved cell (diffuse) lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-Hodgkin lymphoma", "shortest_name_length": 3}
{"curie": "UMLS:C1261962", "names": ["Gastrointestinal erosion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal erosion", "shortest_name_length": 24}
{"curie": "UMLS:C3898089", "names": ["Orbital Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Orbital Melanoma", "shortest_name_length": 16}
{"curie": "MONDO:0043541", "names": ["Viral Conjunctivitis", "CONJUNCTIVITIS VIRAL", "viral conjunctivitis", "Viral conjunctivitis", "Conjunctivitis;viral", "conjunctivitis viral", "Conjunctivitis viral", "Conjunctivitis, Viral", "Conjunctivitis, viral", "Viral Conjunctivitides", "viral Conjunctivitides", "Conjunctivitides, Viral", "Conjunctivitides, viral", "Conjunctivitis viral NOS", "Viral conjunctivitis NOS", "Viral conjunctivitis, NOS", "Viral conjunctivitis (disorder)", "virus; conjunctivitis (etiology)", "Viruses conjunctivitis (disease)", "viral; infection, conjunctivitis", "viral conjunctivitis (diagnosis)", "infection; viral, conjunctivitis", "conjunctivitis; viral (etiology)", "Viral conjunctivitis, unspecified", "conjunctivitis; viral (manifestation)", "virus; conjunctivitis (manifestation)", "Viruses caused conjunctivitis (disease)", "conjunctiva; disorder, viral (etiology)", "conjunctiva; disorder, viral (manifestation)", "disease (or disorder); conjunctiva, viral (etiology)", "disease (or disorder); conjunctiva, viral (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "viral conjunctivitis", "shortest_name_length": 20}
{"curie": "UMLS:C0751776", "names": ["Atypical Inclusion Body Disease", "Atypical Inclusion-Body Disease", "Atypical Inclusion-Body Diseases", "Inclusion-Body Disease, Atypical", "Inclusion-Body Diseases, Atypical"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypical Inclusion-Body Disease", "shortest_name_length": 31}
{"curie": "MONDO:0000935", "names": ["larynx papilloma", "Larynx Papilloma", "laryngeal papilloma", "Laryngeal papilloma", "Papilloma of Larynx", "papilloma of larynx", "Laryngeal Papilloma", "LARYNGEAL PAPILLOMA", "laryngeal papillomas", "Papilloma of the Larynx", "papilloma of the larynx", "larynx squamous papilloma", "squamous papilloma of larynx", "Squamous Papilloma of Larynx", "squamous papilloma of the larynx", "Squamous Papilloma of the Larynx", "Laryngeal Squamous Cell Papilloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "larynx squamous papilloma", "shortest_name_length": 16}
{"curie": "UMLS:C1336320", "names": ["Stage II Subdiaphragmatic Hodgkin Lymphoma Lymphocyte Depleted", "Stage II Subdiaphragmatic Lymphocyte Depleted Hodgkin Lymphoma", "Stage II Subdiaphragmatic Lymphocyte Depleted Hodgkin's Lymphoma", "Stage II Subdiaphragmatic Hodgkin's Lymphoma Lymphocyte Depleted", "Subdiaphragm Stage II Hodgkin's Lymphoma Lymphocyte Depletion Type", "Stage II Subdiaphragmatic Hodgkin's Disease Lymphocyte Depletion Type", "Stage II Subdiaphragmatic Lymphocyte-Depleted Classical Hodgkin Lymphoma", "Stage II Subdiaphragmatic Lymphocyte Depleted Classical Hodgkin Lymphoma", "Stage II Hodgkin's Disease Lymphocyte Depletion Type below the Diaphragm", "Stage II Hodgkin's Lymphoma Lymphocyte Depletion Type below the Diaphragm", "Ann Arbor Stage II Subdiaphragmatic Lymphocyte-Depleted Classic Hodgkin Lymphoma", "Ann Arbor Stage II Subdiaphragmatic Lymphocyte-Depleted Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage II Subdiaphragmatic Lymphocyte-Depleted Classic Hodgkin Lymphoma", "shortest_name_length": 62}
{"curie": "MONDO:0002441", "names": ["JLNS1", "Jervell's syndrome", "SURDO-CARDIAC SYNDROME", "Lange-Nielsen syndrome", "lange-nielsen syndrome", "Surdo Cardiac Syndrome", "Surdo-cardiac syndrome", "Surdo-Cardiac Syndrome", "Syndrome, Surdo-Cardiac", "Surdo-Cardiac Syndromes", "Cardio-auditory syndrome", "jervell lange-nielsen syndrome", "jervell-lange nielsen syndrome", "Jervell Lange-Nielsen syndrome", "jervell lange nielson syndrome", "Jervell-Lange Nielsen syndrome", "Jervell Lange Nielsen Syndrome", "Jervell-Lange Nielsen Syndrome", "Syndrome, Jervell-Lange Nielsen", "Cardio-Auditory-Syncope Syndrome", "Cardio Auditory Syncope Syndrome", "Cardio-auditory-syncope syndrome", "Syndrome, Cardio-Auditory-Syncope", "Cardio-Auditory-Syncope Syndromes", "Jervell and Lange-Nielsen Syndrome", "Jervell and Lange Nielsen Syndrome", "Jervell and Lange-Nielson syndrome", "long QT interval-deafness syndrome", "Syndromes, Cardio-Auditory-Syncope", "Jervell and Lange Nielsen syndrome", "Jervell and Lange-Nielsen syndrome", "Long QT interval-deafness syndrome", "Jervell and Lange-Nielsen syndrome 1", "Long QT interval-hearing loss syndrome", "Jervell and Lange-Nielsen syndrome type 1", "Jervell and Lange-Nielsen syndrome (disorder)", "Prolonged QT Interval in EKG and Sudden Death", "PROLONGED QT INTERVAL IN EKG AND SUDDEN DEATH", "prolonged QT interval in EKG and sudden death", "Deafness, Congenital, and Functional Heart Disease", "DEAFNESS, CONGENITAL, AND FUNCTIONAL HEART DISEASE", "deafness, congenital, and functional heart disease", "Cardioauditory Syndrome of Jervell and Lange-Nielsen", "Cardioauditory Syndrome of Jervell and Lange Nielsen", "CARDIOAUDITORY SYNDROME OF JERVELL AND LANGE-NIELSEN", "Cardioauditory syndrome of Jervell and Lange-Nielsen"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jervell and Lange-Nielsen syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0013339", "names": ["CMD1GG", "dilated cardiomyopathy 1GG", "CARDIOMYOPATHY, DILATED, 1GG", "cardiomyopathy, dilated, 1GG", "dilated cardiomyopathy type 1GG", "cardiomyopathy, dilated, type 1Gg", "SDHA familial isolated dilated cardiomyopathy", "familial isolated dilated cardiomyopathy caused by mutation in SDHA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1GG", "shortest_name_length": 6}
{"curie": "UMLS:C2212625", "names": ["Bladder Embryonal Rhabdomyosarcoma", "embryonal rhabdomyosarcoma of bladder", "embryonal rhabdomyosarcoma of bladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "embryonal rhabdomyosarcoma of bladder", "shortest_name_length": 34}
{"curie": "MONDO:0009236", "names": ["Kandori's syndrome", "Kandori fleck retina", "FLECK RETINA OF KANDORI", "Fleck retina of Kandori", "FLECK retina of KANDORI", "Fleck Retina of Kandori", "Kandori fleck retina syndrome", "Fleck retina of Kandori syndrome", "Flecked retina-night blindness syndrome", "Kandori fleck retina syndrome (disorder)", "Kandori fleck retina syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kandori fleck retina", "shortest_name_length": 18}
{"curie": "MONDO:0015840", "names": ["total septate uterus", "complete septate uterus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complete septate uterus", "shortest_name_length": 20}
{"curie": "MONDO:0043576", "names": ["ENDARTERITIS", "Endarteritis", "endarteritis", "Endarteritides", "Endarteritis NOS", "Endarteritis, NOS", "Endarteritis (disorder)", "endarteritis (diagnosis)", "tunica intima of artery inflammation", "inflammation of tunica intima of artery"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endarteritis", "shortest_name_length": 12}
{"curie": "UMLS:C4683690", "names": ["Noncutaneous Childhood Anaplastic Large Cell Lymphoma by Ann Arbor Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Noncutaneous Childhood Anaplastic Large Cell Lymphoma by Ann Arbor Stage", "shortest_name_length": 72}
{"curie": "MONDO:0017716", "names": ["disorder of carnitine cycle and carnitine transport"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of carnitine cycle and carnitine transport", "shortest_name_length": 51}
{"curie": "MONDO:0003367", "names": ["Gastric leiomyosarcoma", "stomach leiomyosarcoma", "gastric leiomyosarcoma", "STOMACH LEIOMYOSARCOMA", "Gastric Leiomyosarcoma", "GASTRIC LEIOMYOSARCOMA", "leiomyosarcoma of stomach", "Leiomyosarcoma of stomach", "gastric leiomyosarcoma (disease)", "Leiomyosarcoma of stomach (disorder)", "leiomyosarcoma of stomach (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric leiomyosarcoma", "shortest_name_length": 22}
{"curie": "MONDO:0008251", "names": ["PRP", "Devergie's disease", "pityriasis rubra pilaris", "familial pityriasis rubra pilaris", "Familial pityriasis rubra pilaris", "hereditary pityriasis rubra pilaris", "Pityriasis rubra pilaris--familial type", "pityriasis rubra pilaris--familial type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial pityriasis rubra pilaris", "shortest_name_length": 3}
{"curie": "UMLS:C0015256", "names": ["EXCORIATION", "Excoriation", "excoriation", "excoriations", "SKIN EXCORIATION", "Excoriation of skin", "Excoriation of Skin", "excoriation was seen", "Excoriation of skin (disorder)", "excoriation (physical finding)", "Excoriation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Excoriation", "shortest_name_length": 11}
{"curie": "MONDO:0030988", "names": ["DEFDA", "DEVELOPMENTAL DELAY WITH DYSMORPHIC FACIES AND DENTAL ANOMALIES", "developmental delay with dysmorphic facies and dental anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental delay with dysmorphic facies and dental anomalies", "shortest_name_length": 5}
{"curie": "MONDO:0021143", "names": ["melanomas and nevi", "Melanomas and Nevi", "Nevi and Melanomas", "NEVI AND MELANOMAS", "Melanocytic neoplasm", "Melanocytic Neoplasm", "melanocytic neoplasm", "Melanocytic neoplasm (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melanocytic neoplasm", "shortest_name_length": 18}
{"curie": "UMLS:C0030824", "names": ["pcn allergy", "PENICILLIN ALLERGY", "Penicillin Allergy", "penicillin allergy", "Penicillin allergy", "allergy penicillin", "allergy penicillins", "allergies penicillin", "allergy to penicillin", "Allergy to penicillin", "Allergy to penicillin (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Allergy to penicillin", "shortest_name_length": 11}
{"curie": "MONDO:0007074", "names": ["Ainhum", "AINHUM", "ainhum", "Dactylolysis", "ainhum (disease)", "Ainhum (disorder)", "ainhum (diagnosis)", "Dactylysis spontanea", "dactylolysis spontanea", "Dactylolysis spontanea", "Dactylolysis Spontanea", "Spontaneous Dactylolyses", "Spontaneous Dactylolysis", "spontaneous dactylolysis", "Dactylolyses, Spontaneous", "Dactylolysis, Spontaneous", "Ainhum - dactylolysis spontanea"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ainhum", "shortest_name_length": 6}
{"curie": "MONDO:0004729", "names": ["Esophagism", "Oesophagism", "esophagismus", "esophagospasm", "Esophagospasm", "ESOPHAGOSPASM", "esophagospasms", "Oesophagospasm", "OESOPHAGOSPASM", "esophagus spasm", "esophagus spasms", "Esophageal spasm", "esophageal spasm", "Esophageal Spasm", "esophagus; spasm", "spasm esophageal", "Spasm esophageal", "ESOPHAGEAL SPASM", "ESOPHAGUS, SPASM", "oesophagus spasm", "spasm; esophagus", "SPASM ESOPHAGEAL", "esophageal spasms", "Spasm, Esophageal", "Esophageal spasms", "oesophageal spasm", "Curling esophagus", "Spasm;oesophageal", "curling esophagus", "Oesophageal spasm", "Esophageal Spasms", "oesophagus spasms", "Spasm oesophageal", "Spasms, Esophageal", "spasm of esophagus", "Spasm of esophagus", "Curling oesophagus", "oesophageal spasms", "corkscrew esophagus", "spasm of oesophagus", "Spasm of oesophagus", "Corkscrew esophagus", "Corkscrew oesophagus", "dyskinesia esophagus", "Curling of esophagus", "Rosary bead esophagus", "Curling of oesophagus", "ESOPHAGEAL DYSKINESIA", "OS - Esophageal spasm", "ES - Esophageal spasm", "Dyskinesia esophageal", "esophagus; dyskinesia", "Esophageal dyskinesia", "esophageal dyskinesia", "dyskinesia; esophagus", "OS - Oesophageal spasm", "dysmotility esophageal", "ES - Oesophageal spasm", "Esophageal dysmotility", "Esophageal Dysmotility", "ESOPHAGEAL DYSMOTILITY", "esophageal dysmotility", "Dyskinesia oesophageal", "Rosary bead oesophagus", "Dysmotility, Esophageal", "dyskinesia of esophagus", "Dysmotility;oesophageal", "Barsony-Polgar syndrome", "Dyskinesia of esophagus", "oesophageal dysmotility", "Oesophageal dysmotility", "Diffuse esophageal spasm", "Dyskinesia of oesophagus", "diffuse esophageal spasm", "ESOPHAGEAL SPASM DIFFUSE", "Esophageal Dysmotilities", "Esophagus, diffuse spasm", "Diffuse Esophageal Spasm", "dyskinesia of oesophagus", "esophageal motor disorder", "diffuse oesophageal spasm", "diffuse esophageal spasms", "Diffuse oesophageal spasm", "Spasm, Diffuse Esophageal", "Esophageal Spasm, Diffuse", "Dysmotilities, Esophageal", "Esophageal motor disorder", "Diffuse Esophageal Spasms", "Esophageal Spasms, Diffuse", "oesophageal motor disorder", "Oesophageal motor disorder", "disorders esophageal motor", "Spasms, Diffuse Esophageal", "Diffuse spasm of esophagus", "Diffuse spasm of oesophagus", "Esophageal motility disorder", "Esophageal Motility Disorder", "Barsony-Teschendorf syndrome", "esophageal motility disorder", "Esophageal motility disorders", "Disorder, Esophageal Motility", "motility disorders esophageal", "Esophageal Motility Disorders", "Motility Disorder, Esophageal", "Oesophageal motility disorder", "oesophageal motility disorder", "esophageal motility disorders", "curling esophagus (diagnosis)", "DOS - Diffuse esophageal spasm", "Disorders, Esophageal Motility", "Esophageal motor disorder, NOS", "Motility Disorders, Esophageal", "Oesophageal motor disorder, NOS", "corkscrew esophagus (diagnosis)", "DOS - Diffuse oesophageal spasm", "esophageal dyskinesia (diagnosis)", "Esophageal dysmotility (disorder)", "esophageal dysmotility (diagnosis)", "Pseudo-obstruction of the esophagus", "diffuse esophageal spasm (diagnosis)", "Pseudo-obstruction of the oesophagus", "Diffuse spasm of esophagus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyskinesia of esophagus", "shortest_name_length": 10}
{"curie": "MONDO:0000889", "names": ["hemophilus meningitis", "Meningitis hemophilus", "Hemophilus Meningitis", "Hemophilus meningitis", "Meningitis, Hemophilus", "Meningitis haemophilus", "meningitis; Hemophilus", "meningitis haemophilus", "Haemophilus meningitis", "haemophilus meningitis", "Haemophilus Meningitis", "Hemophilus; meningitis", "Hemophilus Meningitides", "Haemophilus; meningitis", "meningitis; Haemophilus", "Meningitis, Haemophilus", "Haemophilus Meningitides", "Meningitides, Hemophilus", "Meningitides, Haemophilus", "Meningitis due to H. influenzae", "Hemophilus influenza meningitis", "hemophilus influenzae meningitis", "meningitis hemophilus influenzae", "Hemophilus influenzae meningitis", "Haemophilus influenzae meningitis", "Haemophilus meningitis (disorder)", "Hemophilus influenzae; meningitis", "haemophilus influenzae meningitis", "Hemophilus meningitis (diagnosis)", "Haemophilus influenzae; meningitis", "Meningitis due to Hemophilus influenzae", "meningitis due to Hemophilus influenzae", "Haemophilus influenzae bacterial meningitis", "Haemophilus influenzae meningitis (disorder)", "meningitis; influenzal (Hemophilus influenzae)", "meningitis; influenzal (Haemophilus influenzae)", "Haemophilus influenzae caused bacterial meningitis", "meningitis due to Hemophilus influenzae (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "haemophilus meningitis", "shortest_name_length": 21}
{"curie": "MONDO:0009124", "names": ["Dubowitz", "Dubowitz Syndrome", "DUBOWITZ SYNDROME", "Dubowitz syndrome", "Dubowitz syndrome 1", "Dubowitz's syndrome", "Dubowitz's syndrome (disorder)", "Dubowitz's syndrome (diagnosis)", "Dwarfism-eczema-peculiar facies syndrome", "dwarfism-eczema-peculiar facies syndrome", "intrauterine growth retardation, short stature, microcephaly, mild mental retardation with behavior problems, eczema, and unusual and distinctive faci", "intrauterine growth retardation, short stature, microcephaly, mild intellectual disability with behavior problems, eczema, and unusual and distinctive faci"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dubowitz syndrome", "shortest_name_length": 8}
{"curie": "UMLS:C0494164", "names": ["Small intestine metastases", "Metastasis to the Small Bowel", "Metastasis to small intestine", "Metastases to Small Intestine", "Metastases to small intestine", "Metastasis to the Small Intestine", "Cancer metastatic to small intestine", "Metastatic Neoplasm to the Small Intestine", "Secondary Malignant Tumor to the Small Bowel", "small intestine neoplasm malignant secondary", "Secondary Malignant Neoplasm to the Small Bowel", "Secondary malignant neoplasm of small intestine", "Metastatic malignant neoplasm to small intestine", "Secondary Malignant Tumor to the Small Intestine", "Metastatic malignant neoplasm of small intestine", "Secondary Malignant Neoplasm to the Small Intestine", "Secondary malignant neoplasm of small intestine, NOS", "Metastatic Malignant Neoplasm in the Small Intestine", "Metastatic Malignant Neoplasm to the Small Intestine", "Metastatic malignant neoplasm to small intestine, NOS", "Secondary malignant neoplasm of small intestine (diagnosis)", "Metastatic malignant neoplasm to small intestine (disorder)", "Secondary malignant neoplasm of small intestine incl duodenum", "Secondary malignant neoplasm of small intestine including duodenum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to small intestine", "shortest_name_length": 26}
{"curie": "MONDO:0000981", "names": ["Histoplasma pericarditis", "Pericarditis histoplasma", "Histoplasmosis pericarditis", "histoplasmosis pericarditis", "acute Histoplasma pericarditis", "histoplasmosis with pericarditis", "Histoplasmosis with pericarditis", "Histoplasma pericarditis (disease)", "Histoplasma caused pericarditis (disease)", "Histoplasmosis, unspecified, pericarditis", "Histoplasmosis with pericarditis (disorder)", "histoplasmosis with pericarditis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Histoplasma pericarditis", "shortest_name_length": 24}
{"curie": "MONDO:0020441", "names": ["right SVC connecting to left-sided atrium", "right superior vena cava connecting to left-sided atrium", "right superior caval vein connecting to left-sided atrium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "right superior vena cava connecting to left-sided atrium", "shortest_name_length": 41}
{"curie": "MONDO:0010277", "names": ["SMRXS", "MRXS11", "Orofaciodigital syndrome, Shashi type", "Mental retardation X-linked Shashi type", "mental retardation X-linked Shashi type", "X-linked mental retardation Shashi type", "Mental retardation X-linked syndromic 11", "mental retardation X-linked syndromic 11", "Mental Retardation, X-Linked, Shashi Type", "MENTAL RETARDATION, X-LINKED, SHASHI TYPE", "mental retardation, X-linked, Shashi type", "MENTAL RETARDATION, X-LINKED, SYNDROMIC 11", "Mental Retardation, X-Linked, Syndromic 11", "mental retardation, X-linked, syndromic 11", "SHASHI X-LINKED MENTAL RETARDATION SYNDROME", "Shashi X-linked mental retardation syndrome", "intellectual disability X-linked Shashi type", "X-linked intellectual disability Shashi type", "intellectual disability X-linked syndromic 11", "X-linked intellectual disability, Shashi type", "intellectual disability, X-linked, Shashi type", "intellectual disability, X-linked, syndromic 11", "Shashi X-linked intellectual disability syndrome", "Syndromic X-linked intellectual disability type 11", "x-linked intellectual disability syndromic type 11", "syndromic X-linked intellectual disability type 11", "syndromic X-linked intellectual disability Shashi type", "mental retardation, X-linked, syndromic 11, Shashi type", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 11", "intellectual disability, X-linked, syndromic 11, Shashi type", "Syndromic X-linked intellectual disability type 11 (disorder)", "Syndromic X-linked intellectual disability type 11 (diagnosis)", "intellectual developmental disorder, syndromic 11, Shashi type, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic X-linked intellectual disability Shashi type", "shortest_name_length": 5}
{"curie": "MONDO:0001032", "names": ["Mooren", "Mooren ulcer", "Mooren; ulcer", "ulcer; Mooren", "Mooren's ulcer", "Mooren's corneal ulcer", "Mooren's ulcer (disorder)", "Mooren's corneal ulceration", "Mooren's corneal ulcer (diagnosis)", "Mooren's corneal ulceration (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mooren ulcer", "shortest_name_length": 6}
{"curie": "UMLS:C4288936", "names": ["PHA Type 2", "Gordon Hyperkalemia", "Chloride Shunt Syndrome", "Spitzer-Weinstein Syndrome", "Pseudohypoaldosteronism, Type II", "Familial Hyperkalemic Hypertension", "Mineralocorticoid Resistant Hyperkalemia", "Hyperkalemic Mineralocorticoid Resistance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyperkalemic Mineralocorticoid Resistance", "shortest_name_length": 10}
{"curie": "UMLS:C5670661", "names": ["CNS Ewing Sarcoma", "Central Nervous System Ewing Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Ewing Sarcoma", "shortest_name_length": 17}
{"curie": "MONDO:0010219", "names": ["XYLOSIDASE DEFICIENCY", "Xylosidase Deficiency", "xylosidase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "xylosidase deficiency", "shortest_name_length": 21}
{"curie": "MONDO:0020457", "names": ["PGDD", "6PGD DEFICIENCY", "6-PHOSPHOGLUCONATE DEHYDROGENASE DEFICIENCY", "6-phosphogluconate dehydrogenase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "6-phosphogluconate dehydrogenase deficiency", "shortest_name_length": 4}
{"curie": "UMLS:C4682798", "names": ["Stage 0 Testicular Cancer", "Stage 0 Testicular Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Testicular Cancer AJCC v8", "shortest_name_length": 25}
{"curie": "UMLS:C0277528", "names": ["Turista", "turista", "diarrhea travelers", "Travelers' diarrhea", "Traveler's diarrhea", "traveler's diarrhea", "diarrhea travelers'", "diarrhea traveler's", "travelers' diarrhea", "Traveller's diarrhea", "Traveler's diarrhoea", "diarrhoea travellers", "traveller's diarrhea", "Traveller's diarrhoea", "traveller's diarrhoea", "Travellers' diarrhoea", "Traveler's diarrhea (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Traveler's diarrhea", "shortest_name_length": 7}
{"curie": "UMLS:C2717792", "names": ["Airway Remodeling", "Airway remodeling", "Airway remodelling", "Airway Remodelings", "Remodeling, Airway", "Airway Remodelling", "Airway Remodellings", "Remodelings, Airway", "Remodelling, Airway", "Remodellings, Airway", "Airway Wall Remodelling", "Remodelling, Airway Wall", "Airway Wall Remodellings", "Wall Remodelling, Airway", "Remodellings, Airway Wall", "Wall Remodellings, Airway"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Airway Remodeling", "shortest_name_length": 17}
{"curie": "UMLS:C3273034", "names": ["Moderately Differentiated Hepatocellular Cancer", "Moderately Differentiated Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Moderately Differentiated Hepatocellular Carcinoma", "shortest_name_length": 47}
{"curie": "MONDO:0003951", "names": ["Scrotal Angioma", "scrotal angioma", "scrotal hemangioma", "angioma of scrotum", "Angioma of Scrotum", "Scrotal Hemangioma", "scrotum hemangioma", "Hemangioma of Scrotum", "hemangioma of scrotum", "Angioma of the Scrotum", "angioma of the scrotum", "hemangioma of the scrotum", "Hemangioma of the Scrotum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scrotal hemangioma", "shortest_name_length": 15}
{"curie": "UMLS:C4744802", "names": ["Thyroid Gland Langerhans Cell Histiocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Langerhans Cell Histiocytosis", "shortest_name_length": 43}
{"curie": "MONDO:0003285", "names": ["fallopian tube leiomyoma", "Fallopian Tube Leiomyoma", "Fallopian tube leiomyoma", "leiomyoma of fallopian tube"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fallopian tube leiomyoma", "shortest_name_length": 24}
{"curie": "MONDO:0019989", "names": ["pauci-immune glomerulonephritis without ANCA", "pauci-immune glomerulonephritis without antineutrophil cytoplasmic antibody", "antineutrophil cytoplasmic antibody-negative pauci-immune glomerulonephritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pauci-immune glomerulonephritis without ANCA", "shortest_name_length": 44}
{"curie": "UMLS:C3273070", "names": ["Bile Duct MCN with Intermediate Grade Intraepithelial Neoplasia", "Bile Duct Mucinous Cystic Neoplasm with Intermediate Grade Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bile Duct Mucinous Cystic Neoplasm with Intermediate Grade Intraepithelial Neoplasia", "shortest_name_length": 63}
{"curie": "MONDO:0030454", "names": ["JBTS39", "Joubert syndrome 39", "JOUBERT SYNDROME 39"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome 39", "shortest_name_length": 6}
{"curie": "MONDO:0011323", "names": ["BAMS", "Bosma syndrome", "Gifford Bosma syndrome", "Ruprecht Majewski syndrome", "BOSMA ARHINIA MICROPHTHALMIA SYNDROME", "BOSMA arhinia microphthalmia syndrome", "Bosma arhinia microphthalmia syndrome", "Arhinia, choanal atresia and microphthalmia", "Arhinia, choanal atresia, and microphthalmia", "arhinia, choanal atresia, and microphthalmia", "BAMS - Bosma arhinia microphthalmia syndrome", "Arrhinia-choanal atresia-microphthalmia syndrome", "arrhinia-choanal atresia-microphthalmia syndrome", "Arrhinia with choanal atresia and microphthalmia syndrome", "Arrhinia with choanal atresia and microphthalmia syndrome (disorder)", "Arhinia, choanal atresia, microphthalmia, and hypogonadotropic hypogonadism", "arhinia, choanal atresia, microphthalmia, and hypogonadotropic hypogonadism", "ARHINIA, CHOANAL ATRESIA, MICROPHTHALMIA, AND HYPOGONADOTROPIC HYPOGONADISM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arhinia, choanal atresia, and microphthalmia", "shortest_name_length": 4}
{"curie": "UMLS:C4525695", "names": ["Stage III Appendix Neuroendocrine Tumor", "Stage III Appendix Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Appendix Neuroendocrine Tumor AJCC v8", "shortest_name_length": 39}
{"curie": "UMLS:C0856695", "names": ["acute chronic bronchitis", "acute on chronic bronchitis", "Acute on chronic bronchitis", "Acute exacerbation of chronic bronchitis", "chronic bronchitis with acute exacerbation", "BRONCHITIS CHRONIC WITH ACUTE EXACERBATION", "Acute exacerbation of chronic bronchitis NOS", "Acute exacerbation of chronic bronchitis (disorder)", "chronic bronchitis with acute exacerbation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute exacerbation of chronic bronchitis", "shortest_name_length": 24}
{"curie": "MONDO:0013402", "names": ["RP27", "retinitis pigmentosa 27", "RETINITIS PIGMENTOSA 27", "Retinitis Pigmentosa 27", "NRL retinitis pigmentosa", "retinitis pigmentosa type 27", "retinitis pigmentosa caused by mutation in NRL", "RETINAL DEGENERATION, AUTOSOMAL RECESSIVE, CLUMPED PIGMENT TYPE", "retinal Degeneration, autosomal recessive, Clumped pigment type", "Retinal Degeneration, Autosomal Recessive, Clumped Pigment Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 27", "shortest_name_length": 4}
{"curie": "MONDO:0044777", "names": ["POF14", "premature ovarian failure 14", "PREMATURE OVARIAN FAILURE 14", "primary ovarian insufficiency 14", "GDF9-related primary ovarian insufficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "premature ovarian failure 14", "shortest_name_length": 5}
{"curie": "UMLS:C1709884", "names": ["Regional Adrenal Gland Chromaffinoma", "Regional Adrenal Gland Chromaffin Tumor", "Regional Adrenal Gland Pheochromocytoma", "Regional Adrenal Gland Chromaffin Neoplasm", "Regional Adrenal Gland Chromaffin Paraganglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Regional Adrenal Gland Pheochromocytoma", "shortest_name_length": 36}
{"curie": "UMLS:C0451769", "names": ["Heavy-Metal-Induced Nephropathy", "Nephropathy due to heavy metals", "toxic; nephropathy, heavy metals", "nephropathy; heavy metal-induced", "nephropathy; toxic, heavy metals", "Nephropathy caused by heavy metals", "nephropathy induced by heavy metals", "Nephropathy induced by heavy metals", "Nephropathy caused by heavy metals (disorder)", "nephropathy induced by heavy metals (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephropathy induced by heavy metals", "shortest_name_length": 31}
{"curie": "MONDO:0008588", "names": ["GSM1", "GSM 1", "Geniospasm", "geniospasm", "Chin spasms", "GENIOSPASM 1", "geniospasm 1", "Geniospasm 1", "Chin myoclonus", "TREMBLING CHIN", "trembling Chin", "Trembling chin", "hereditary geniospasm", "Hereditary geniospasm", "Hereditary chin myoclonus", "Hereditary chin-trembling", "Hereditary chin trembling", "hereditary chin-trembling", "hereditary chin myoclonus", "Familial trembling of chin", "familial trembling of the chin", "Familial trembling of the chin", "Hereditary geniospasm (disorder)", "hereditary chin tremor/myoclonus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary geniospasm", "shortest_name_length": 4}
{"curie": "UMLS:C4745063", "names": ["Biliary Tract Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Biliary Tract Carcinoma", "shortest_name_length": 23}
{"curie": "UMLS:C0205622", "names": ["Microinvasive", "Microinvasive tumor", "Microinvasive tumour", "Microinvasive Lesion", "Microinvasive tumor (qualifier value)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Microinvasive tumor", "shortest_name_length": 13}
{"curie": "UMLS:C0349774", "names": ["Diverticulitis of gastrointestinal tract", "Diverticulitis of gastrointestinal tract (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diverticulitis of gastrointestinal tract", "shortest_name_length": 40}
{"curie": "UMLS:C1514506", "names": ["Prostate Adenocarcinoma with Neuroendocrine Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Adenocarcinoma with Neuroendocrine Differentiation", "shortest_name_length": 59}
{"curie": "MONDO:0042458", "names": ["Trichinella spiralis infection", "Trichinella spiralis infectious disease", "Trichinella spiralis disease or disorder", "trichinosis caused by Trichinella spiralis", "Trichinosis caused by Trichinella spiralis", "Infection by larvae of Trichinella spiralis", "trichiniasis caused by Trichinella spiralis", "infection by larvae of Trichinella spiralis", "Trichiniasis caused by Trichinella spiralis", "Trichinellosis caused by Trichinella spiralis", "trichinellosis caused by Trichinella spiralis", "Trichinelliasis caused by Trichinella spiralis", "trichinelliasis caused by Trichinella spiralis", "Trichinella spiralis caused disease or disorder", "infection caused by larvae of Trichinella spiralis", "Infection caused by larvae of Trichinella spiralis", "Infection caused by larvae of Trichinella spiralis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Trichinella spiralis infectious disease", "shortest_name_length": 30}
{"curie": "MONDO:0015807", "names": ["Myopic maculopathy", "myopic maculopathy", "Myopic macular degeneration", "myopic macular degeneration", "myopic degeneration of macula", "degeneration of macula myopic", "Myopic macular degeneration (disorder)", "myopic degeneration of macula (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopic macular degeneration", "shortest_name_length": 18}
{"curie": "MONDO:0013048", "names": ["SPG50", "CPSQ3, FORMERLY", "AP-4 deficiency syndrome", "hereditary spastic paraplegia 50", "AP4M1 hereditary spastic paraplegia", "adaptor protein complex 4 deficiency", "hereditary spastic paraplegia type 50", "spastic quadriplegic cerebral palsy 3", "cerebral palsy, spastic quadriplegic, 3", "autosomal recessive spastic paraplegia 50", "spastic paraplegia 50, autosomal recessive", "Spastic Paraplegia-50, Autosomal Recessive", "SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE", "AP-4-Associated Hereditary Spastic Paraplegia", "cerebral palsy, spastic quadriplegic, 3, formerly", "CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3, FORMERLY", "hereditary spastic paraplegia caused by mutation in AP4M1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 50", "shortest_name_length": 5}
{"curie": "UMLS:C4329633", "names": ["Central Nervous System Intravascular Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Intravascular Large B-Cell Lymphoma", "shortest_name_length": 58}
{"curie": "UMLS:C4528641", "names": ["Stage IV Low-CSD Melanoma AJCC v7", "Stage IV Superficial Spreading Melanoma", "Stage IV Superficial Spreading Melanoma AJCC v6 and v7", "Stage IV Superficial Spreading Cutaneous (Skin) Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Low-CSD Melanoma AJCC v7", "shortest_name_length": 33}
{"curie": "UMLS:C1333851", "names": ["Grade 3b Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade 3b Malignant Neoplasm", "shortest_name_length": 27}
{"curie": "UMLS:C4528633", "names": ["Stage I Acral Melanoma AJCC v7", "Stage I Acral Lentiginous Melanoma", "Stage I Acral Lentiginous Melanoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Acral Lentiginous Melanoma AJCC v7", "shortest_name_length": 30}
{"curie": "MONDO:0004868", "names": ["biliary tree disease", "Biliary Tract Disease", "biliary tract disease", "Biliary tract disease", "biliary disease tract", "Tract Disease, Biliary", "biliary tract disorder", "Biliary Tract Diseases", "Biliary tract disorder", "Disease, Biliary Tract", "biliary tract diseases", "biliary tract disorders", "Diseases, Biliary Tract", "disease of biliary tree", "Tract Diseases, Biliary", "Biliary tract--Diseases", "disorder of biliary tree", "Disease of biliary tract", "Disease of biliary system", "BILIARY TRACT ABNORMALITY", "Disorder of biliary tract", "Biliary tract abnormality", "Biliary tract disorder NOS", "BILIARY TRACT DISEASE, NOS", "Hepatobiliary tract disease", "Disease of biliary tract, NOS", "biliary tree disease or disorder", "biliary and gallbladder disorder", "biliary tract disease (diagnosis)", "disease or disorder of biliary tree", "Disorder of biliary tract (disorder)", "Unspecified disorder of biliary tract", "Disease of biliary tract, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "biliary tract disorder", "shortest_name_length": 20}
{"curie": "UMLS:C5667236", "names": ["Recurrent Glioblastoma, IDH-Wildtype"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Glioblastoma, IDH-Wildtype", "shortest_name_length": 36}
{"curie": "MONDO:0005568", "names": ["trash foot", "Trash foot", "atheroembolism", "Atheroembolism", "Atheroembolisms", "Cholesterol embolus", "cholesterol embolus", "purple toe syndrome", "Atheromatous embolus", "cholesterol embolism", "CHOLESTEROL EMBOLISM", "Embolus, cholesterol", "Cholesterol Embolism", "ATHEROMATOUS EMBOLISM", "Cholesterol Embolisms", "Embolism, Cholesterol", "Trash foot (disorder)", "Embolus, atheromatous", "Embolisms, Cholesterol", "Trash foot (diagnosis)", "warfarin blue toe syndrome", "atheroembolism (diagnosis)", "cholesterol crystal embolism", "lower limb ischemia foot trash", "cholesterol embolus (physical finding)", "Atheromatous embolus (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholesterol embolism", "shortest_name_length": 10}
{"curie": "UMLS:C0521500", "names": ["Injection site extravasation", "Injection site extravasation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site extravasation", "shortest_name_length": 28}
{"curie": "MONDO:0004271", "names": ["lactate adenoma", "Lactating Adenoma", "Lactating adenoma", "lactating adenoma", "pregnancy adenoma", "Pregnancy Adenoma", "Lactating adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pregnancy adenoma", "shortest_name_length": 15}
{"curie": "MONDO:0008354", "names": ["PURPURA SIMPLEX", "simplex purpura", "purpura simplex", "Purpura simplex", "Simple bruising", "purpura; simplex", "Purpura, simplex", "simplex; purpura", "Purpura simplex (disorder)", "simplex purpura (diagnosis)", "Hereditary familial purpura simplex"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "purpura simplex", "shortest_name_length": 15}
{"curie": "MONDO:0012276", "names": ["GEPD", "PNKD3", "paroxysmal nonkinesigenic dyskinesia 3", "Generalized Epilepsy and Paroxysmal Dyskinesia", "generalized epilepsy and paroxysmal dyskinesia", "GENERALIZED EPILEPSY AND PAROXYSMAL DYSKINESIA", "epilepsy, generalized, with paroxysmal dyskinesia", "Epilepsy, Generalized, with Paroxysmal Dyskinesia", "Generalized epilepsy-paroxysmal dyskinesia syndrome", "generalized epilepsy-paroxysmal dyskinesia syndrome", "Generalised epilepsy and paroxysmal dyskinesia syndrome", "Generalized epilepsy and paroxysmal dyskinesia syndrome", "epilepsy generalized and paroxysmal dyskinesia syndrome", "Generalized epilepsy and paroxysmal dyskinesia syndrome (disorder)", "Generalized epilepsy and paroxysmal dyskinesia syndrome (diagnosis)", "PAROXYSMAL NONKINESIGENIC DYSKINESIA, 3, WITH OR WITHOUT GENERALIZED EPILEPSY", "paroxysmal nonkinesigenic dyskinesia, 3, with or without generalized epilepsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "generalized epilepsy-paroxysmal dyskinesia syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0011249", "names": ["TORSION DYSTONIA WITH ONSET IN INFANCY", "Torsion dystonia with onset in infancy", "torsion dystonia with onset in infancy", "Autosomal dominant torsion dystonia with onset in infancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "torsion dystonia with onset in infancy", "shortest_name_length": 38}
{"curie": "MONDO:0015874", "names": ["benign ductal tumor of breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign ductal tumor of breast", "shortest_name_length": 29}
{"curie": "MONDO:0018829", "names": ["familial schizencephaly", "Familial schizencephaly", "hereditary schizencephaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial schizencephaly", "shortest_name_length": 23}
{"curie": "MONDO:0009541", "names": ["Lymphopenic Hypergammaglobulinemia, Antibody Deficiency, Autoimmune Hemolytic Anemia, and Glomerulonephritis", "lymphopenic hypergammaglobulinemia, antibody deficiency, autoimmune hemolytic anemia, and glomerulonephritis", "LYMPHOPENIC HYPERGAMMAGLOBULINEMIA, ANTIBODY DEFICIENCY, AUTOIMMUNE HEMOLYTIC ANEMIA, AND GLOMERULONEPHRITIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphopenic hypergammaglobulinemia, antibody deficiency, autoimmune hemolytic anemia, and glomerulonephritis", "shortest_name_length": 108}
{"curie": "MONDO:0011510", "names": ["BOS", "BOPS", "BOS syndrome", "Bos syndrome", "C-like syndrome", "C-LIKE SYNDROME", "Bohring syndrome", "BOHRING SYNDROME", "BOHRING-OPITZ SYNDROME", "BOHRING-Opitz syndrome", "Bohring-Opitz syndrome", "Bohring-Opitz Syndrome", "Bohring Opitz syndrome", "Oberklaid-Danks syndrome", "Bohring Opitz syndrome (disorder)", "OPITZ TRIGONOCEPHALY-LIKE SYNDROME", "Opitz trigonocephaly-like syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bohring-Opitz syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0019280", "names": ["Hairiness", "POLYTRICHIA", "excess hair", "Polytrichia", "polytrichia", "Polytrichosis", "Hypertrichosis", "HYPERTRICHOSIS", "hypertrichosis", "Hypertrichoses", "Hypertrichiasis", "HYPERTRICHIASIS", "Polytrichia, NOS", "Polytrichosis, NOS", "Hypertrichosis NOS", "excessive hairiness", "Hypertrichosis, NOS", "Excessive hairiness", "Hypertrichiasis, NOS", "Excessive hair growth", "excessive; hair growth", "polytrichia (diagnosis)", "Excessive growth of hair", "hypertrichosis (disease)", "Hypertrichosis (disorder)", "hypertrichosis (diagnosis)", "Hirsutism - hypertrichosis", "hypertrichosis polytrichia", "Hypertrichosis (hirsutism)", "Hypertrichosis, unspecified", "Increased hair growth on body", "Excessive hair growth (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrichosis", "shortest_name_length": 9}
{"curie": "UMLS:C2986700", "names": ["Stage II Ovarian Low Malignant Potential Tumor", "stage II ovarian low malignant potential tumor", "stage II ovarian tumors of low malignant potential", "ovarian tumors of low malignant potential, stage II", "Stage II Borderline Ovarian Surface Epithelial-Stromal Tumor", "stage II borderline ovarian surface epithelial-stromal tumor", "borderline ovarian surface epithelial-stromal tumor, stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Borderline Ovarian Surface Epithelial-Stromal Tumor", "shortest_name_length": 46}
{"curie": "UMLS:C0278779", "names": ["Relapsed Osteosarcoma", "Osteosarcoma recurrent", "recurrent osteosarcoma", "Recurrent Osteosarcoma", "Osteosarcoma, Recurrent", "osteosarcoma, recurrent", "Relapsed Osteogenic Sarcoma", "Recurrent Osteogenic Sarcoma", "Osteogenic sarcoma recurrent", "recurrent osteogenic sarcoma", "sarcoma, recurrent osteogenic", "osteogenic sarcoma, recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Osteosarcoma recurrent", "shortest_name_length": 21}
{"curie": "UMLS:C0920045", "names": ["thrombus on catheter", "Thrombus in Catheter", "Thrombus in catheter", "thrombus on the catheter", "thrombus on catheter (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thrombus in catheter", "shortest_name_length": 20}
{"curie": "EFO:1001493", "names": ["cardiac embolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiac embolism", "shortest_name_length": 16}
{"curie": "MONDO:0003231", "names": ["nonparalytic poliomyelitis", "non-paralytic aseptic meningitis", "acute nonparalytic poliomyelitis", "Acute nonparalytic poliomyelitis", "Acute non-paralytic poliomyelitis", "Anterior acute poliomyelitis, nonparalytic", "Epidemic acute poliomyelitis, non paralytic", "Acute nonparalytic poliomyelitis (disorder)", "Anterior acute poliomyelitis specified as nonparalytic", "Epidemic acute poliomyelitis specified as non paralytic", "Acute nonparalytic poliomyelitis, poliovirus, unspecified type", "Acute non-paralytic poliomyelitis, unspecified type poliovirus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute nonparalytic poliomyelitis", "shortest_name_length": 26}
{"curie": "EFO:1001436", "names": ["thyroid nodule"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid nodule", "shortest_name_length": 14}
{"curie": "UMLS:C0858911", "names": ["Blood pressure immeasurable"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Blood pressure immeasurable", "shortest_name_length": 27}
{"curie": "UMLS:C5239116", "names": ["Relapsed HER2 Negative Breast Carcinoma", "Recurrent HER2 Negative Breast Carcinoma", "Recurrent HER2-Negative Breast Carcinoma", "Recurrent HER2 Negative Breast Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent HER2-Negative Breast Carcinoma", "shortest_name_length": 39}
{"curie": "UMLS:C1334641", "names": ["Mature Teratoma of Testis", "testicular mature teratoma", "Testicular Mature Teratoma", "Mature Testicular Teratoma", "Mature Teratoma of the Testis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mature Testicular Teratoma", "shortest_name_length": 25}
{"curie": "MONDO:0024571", "names": ["AIDS-related disease", "AIDS-Related Disorder", "AIDS-related disorder", "AIDS related complication", "AIDS-related complications", "Disease Associated with AIDS", "disease associated with AIDS", "AIDS related complication NOS", "AIDS/HIV - RelatedDisease Associated with AIDS", "AIDS/HIV - relatedDisease associated with AIDS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-related disorder", "shortest_name_length": 20}
{"curie": "MONDO:0044211", "names": ["Urticaria idiopathic", "urticaria idiopathic", "idiopathic urticaria", "Idiopathic urticaria", "urticaria; idiopathic", "idiopathic; urticaria", "Idiopathic urticaria (disorder)", "idiopathic urticaria angioedema", "idiopathic angioedema-urticaria", "idiopathic urticaria (diagnosis)", "Idiopathic angio-edema-urticaria", "Idiopathic angio-oedema-urticaria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic urticaria", "shortest_name_length": 20}
{"curie": "MONDO:0008830", "names": ["AGU", "Aga deficiency", "AGA DEFICIENCY", "AGA Deficiency", "Deficiency, AGA", "AGA Deficiencies", "Deficiencies, AGA", "Glycoasparaginase", "GLYCOASPARAGINASE", "ASPARTYLGLUCOSAMINURIA", "aspartylglycosaminuria", "Aspartylglucosaminuria", "ASPARTYLGLYCOSAMINURIA", "Aspartylglycosaminuria", "aspartylglucosaminuria", "Aspartylglucosaminurias", "Aspartylglycosaminurias", "Glycoasparaginase Deficiency", "aspartylglucosaminuria (AGU)", "Deficiency, Glycoasparaginase", "Glycoasparaginase Deficiencies", "glycosylasparaginase deficiency", "Deficiencies, Glycoasparaginase", "GLYCOSYLASPARAGINASE DEFICIENCY", "Glycosylasparaginase deficiency", "aspartylglucosamidase deficiency", "Aspartylglucosamidase Deficiency", "Aspartylglucosaminuria (disorder)", "Deficiency, Aspartylglucosamidase", "Aspartylglucosaminidase Deficiency", "Aspartylglucosaminidase deficiency", "ASPARTYLGLUCOSAMINIDASE DEFICIENCY", "aspartylglucosaminidase deficiency", "Aspartylglycosylaminase deficiency", "aspartylglucosaminuria (diagnosis)", "Aspartylglucosamidase Deficiencies", "Deficiencies, Aspartylglucosamidase", "High urine aspartylglucosamine levels", "aspartylglucosamidase (AGA) deficiency", "Aspartylglucosamidase (AGA) deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aspartylglucosaminuria", "shortest_name_length": 3}
{"curie": "UMLS:C0920562", "names": ["infection related neoplasm", "Infection-Related Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infection-Related Neoplasm", "shortest_name_length": 26}
{"curie": "MONDO:0044970", "names": ["mitochondrial disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial disease", "shortest_name_length": 21}
{"curie": "MONDO:0003934", "names": ["Apocrine Breast Carcinoma", "Breast Apocrine Carcinoma", "breast apocrine carcinoma", "Apocrine breast carcinoma", "apocrine breast carcinoma", "Apocrine Carcinoma of Breast", "apocrine carcinoma of breast", "breast apocrine adenocarcinoma", "apocrine carcinoma of the breast", "Apocrine Carcinoma of the Breast", "apocrine adenocarcinoma of breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast apocrine carcinoma", "shortest_name_length": 25}
{"curie": "UMLS:C4524377", "names": ["Locally Advanced Solid Tumor", "Locally Advanced Solid Neoplasm", "Locally Advanced Malignant Solid Tumor", "Locally Advanced Malignant Solid Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Malignant Solid Neoplasm", "shortest_name_length": 28}
{"curie": "UMLS:C4289927", "names": ["Uterine Corpus Benign PEComa", "Benign Uterine Corpus PEComa", "Benign Uterine Corpus Perivascular Epithelioid Cell Tumor", "Uterine Corpus Benign Perivascular Epithelioid Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Uterine Corpus PEComa", "shortest_name_length": 28}
{"curie": "MONDO:0011357", "names": ["ECCRINE SYRINGOFIBROADENOMATOSIS WITH EYELID ABNORMALITIES", "eccrine syringofibroadenomatosis with eyelid abnormalities", "Eccrine Syringofibroadenomatosis with Eyelid Abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eccrine syringofibroadenomatosis with eyelid abnormalities", "shortest_name_length": 58}
{"curie": "MONDO:0002361", "names": ["Ca transverse colon", "transverse colon cancer", "Transverse colon cancer", "cancer of transverse colon", "Cancer of transverse colon", "Malignant tumor of transverse colon", "malignant tumor of transverse colon", "malignant transverse colon neoplasm", "Malignant tumour of transverse colon", "malignant neoplasm of transverse colon", "Malignant neoplasm of transverse colon", "Malignant tumor of transverse colon (disorder)", "malignant neoplasm of transverse colon (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transverse colon cancer", "shortest_name_length": 19}
{"curie": "MONDO:0100023", "names": ["self-limited familial neonatal epilepsy", "self-limited familial neonatal-infantile epilepsy", "self-limited familial and non-familial neonatal seizures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "self-limited familial neonatal epilepsy", "shortest_name_length": 39}
{"curie": "MONDO:0005957", "names": ["Setariosis", "setariasis", "Setariasis", "Setariases", "Infection by Setaria", "Infection by Setaria, NOS", "Infection caused by Setaria", "infectious disease by Setaria", "Infectious Disease by Setaria", "Setaria <nematode> infectious disease", "Setaria <nematode> disease or disorder", "Infection caused by Setaria (disorder)", "Setaria <nematode> caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "setariasis", "shortest_name_length": 10}
{"curie": "MONDO:0020601", "names": ["mosquito-borne encephalitis", "Mosquito-Borne Encephalitis", "Mosquito-borne encephalitis", "encephalitis mosquito-borne", "Mosquito Borne Encephalitis", "Encephalitis, Mosquito Borne", "Encephalitis, Mosquito-Borne", "Mosquito-Borne Encephalitides", "Encephalitides, Mosquito-Borne", "Mosquito-borne viral encephalitis", "Mosquito-Borne Viral Encephalitis", "mosquito-borne viral encephalitis", "Mosquito-borne viral encephalitis, NOS", "viral encephalitis due to mosquito-borne virus", "Mosquito-borne viral encephalitis, unspecified", "encephalitis; viral, arthropod-borne, mosquito-borne", "viral; encephalitis, arthropod-borne, mosquito-borne", "Mosquito-borne viral encephalitis (navigational concept)", "viral encephalitis due to mosquito-borne virus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mosquito-borne viral encephalitis", "shortest_name_length": 27}
{"curie": "UMLS:C0264523", "names": ["calcification lung", "lung calcification", "calcification lungs", "calcification; lung", "lung; calcification", "calcifications lung", "calcifications lungs", "Calcification of lung", "calcification of lung", "Pulmonary ossification", "Pulmonary calcification", "pulmonary calcification", "Pulmonary mineralisation", "pulmonary; calcification", "Pulmonary mineralization", "Calcification of lung (disorder)", "calcification of lung (diagnosis)", "Pulmonary ossification (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Calcification of lung", "shortest_name_length": 18}
{"curie": "MONDO:0017525", "names": ["unilateral PPD2", "preaxial polydactyly type 2, unilateral", "polydactyly of a triphalangeal thumb, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polydactyly of a triphalangeal thumb, unilateral", "shortest_name_length": 15}
{"curie": "MONDO:0006446", "names": ["testis cancer, embryonal", "testis embryonal carcinoma", "embryonal testis carcinoma", "testicle cancer, embryonal", "TESTIS, CARCINOMA, EMBRYONAL", "testicular cancer, embryonal", "Embryonal carcinoma of testis", "embryonal carcinoma of testis", "Embryonal Carcinoma of Testis", "testicular embryonal carcinoma", "Testicular Embryonal Carcinoma", "Testicular embryonal carcinoma", "embryonal carcinoma, testicular", "Embryonal Carcinoma of the Testis", "embryonal carcinoma of the testis", "Testicular embryonal carcinoma NOS", "TESTICULAR CANCER, EMBRYONAL CARCINOMA", "embryonal carcinoma of testis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular embryonal carcinoma", "shortest_name_length": 24}
{"curie": "OMIM:613098", "names": ["INCREASED ANALGESIA FROM KAPPA-OPIOID RECEPTOR AGONIST, FEMALE-SPECIFIC", "INCREASED ANALGESIA FROM KAPPA-OPIOID RECEPTOR AGONIST, FEMALE-SPECIFIC (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 71}
{"curie": "UMLS:C1705254", "names": ["Neonatal deformity", "Neonatal Deformity", "Congenital Deformity", "Neonatal Deformities", "Neonatal Malformation", "Congenital Deformation", "Congenital Malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neonatal Deformity", "shortest_name_length": 18}
{"curie": "MONDO:0016028", "names": ["Mitchell", "erythralgia", "Erythralgia", "Erythermalgia", "erythermalgia", "ERYTHERMALGIA", "Erythermalgias", "Erythromelalgia", "ERYTHROMELALGIA", "erythromelalgia", "MITCHELL DISEASE", "gerhardt disease", "Erythromelalgias", "mitchell disease", "GERHARDT DISEASE", "Mitchell's disease", "Weir-Mitchell disease", "WEIR MITCHELL SYNDROME", "Weir Mitchell's disease", "weir mitchell's disease", "Erythromelalgia (disorder)", "erythromelalgia (diagnosis)", "erythromelalgia (red burning extremities)", "erythromelalgia (red burning extremities) (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythromelalgia", "shortest_name_length": 8}
{"curie": "MONDO:0017079", "names": ["cranial meningocele", "Cranial meningocele", "Cranial Meningocele", "CRANIAL MENINGOCELE", "meningoencephalocele", "meningocele cerebral", "Encephalomeningocele", "MENINGOENCEPHALOCELE", "encephalomeningocele", "Cerebral meningocele", "cerebral meningocele", "Meningoencephalocele", "Meningocele, cerebral", "meningocele, cerebral", "Hydrencephalomeningocele", "Cranial hydromeningocele", "Congenital cranial meningocele", "Congenital cerebral meningocele", "Meningoencephalocele (disorder)", "congenital cerebral meningocele", "cranial meningocele (diagnosis)", "cerebral meningocele (diagnosis)", "meningoencephalocele (diagnosis)", "brain meninx cephalocele (disease)", "cephalocele (disease) of brain meninx", "Congenital cerebral meningocele (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "meningoencephalocele", "shortest_name_length": 19}
{"curie": "MONDO:0012464", "names": ["CORD10", "CONE-ROD DYSTROPHY 10", "Cone-Rod Dystrophy 10", "cone-rod dystrophy 10", "SEMA4A cone-rod dystrophy", "cone-rod dystrophy type 10", "cone-rod dystrophy caused by mutation in SEMA4A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cone-rod dystrophy 10", "shortest_name_length": 6}
{"curie": "UMLS:C5206640", "names": ["Penile Lymphoma", "Lymphoma of the Penis", "Primary Penile Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Penile Lymphoma", "shortest_name_length": 15}
{"curie": "UMLS:C3273120", "names": ["Gallbladder NET G2", "Gallbladder Neuroendocrine Tumor G2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gallbladder Neuroendocrine Tumor G2", "shortest_name_length": 18}
{"curie": "MONDO:0000639", "names": ["cartilage cancer", "cartilaginous cancer", "cartilage tissue cancer", "cancer of cartilage tissue", "malignant cartilage tissue neoplasm", "malignant neoplasm of cartilage tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cartilage cancer", "shortest_name_length": 16}
{"curie": "UMLS:C5418918", "names": ["Refractory Primary Peritoneal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Primary Peritoneal Adenocarcinoma", "shortest_name_length": 44}
{"curie": "MONDO:0014823", "names": ["IHPRF3", "TBCK-related intellectual disability syndrome", "TBC1 domain containing kinase-related intellectual disability syndrome", "hypotonia, infantile, with psychomotor retardation and characteristic facies 3", "HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3", "TBC1 domain containing kinase-related intellectual disability syndrome (disorder)", "hypotonia, infantile, with psychomotor retardation and characteristic facies type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotonia, infantile, with psychomotor retardation and characteristic facies 3", "shortest_name_length": 6}
{"curie": "MONDO:0010001", "names": ["RODRIGUES BLINDNESS", "Rodrigues blindness", "RODRIGUES blindness", "ectodermal dysplasia-blindness syndrome", "microphthalmos, microcornea, and sclerocornea with short stature and hair and dental abnormalities", "MICROPHTHALMIA, MICROCORNEA, AND SCLEROCORNEA WITH SHORT STATURE AND HAIR AND DENTAL ABNORMALITIES", "microphthalmia, microcornea, and sclerocornea with short stature and hair and dental abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia-blindness syndrome", "shortest_name_length": 19}
{"curie": "UMLS:C0279604", "names": ["Mixed osteosarcoma", "Mixed Osteosarcoma", "mixed osteosarcoma", "osteosarcoma, mixed", "Mixed Type Osteosarcoma", "mixed type osteosarcoma", "mixed osteogenic sarcoma", "sarcoma, osteogenic mixed", "osteogenic sarcoma, mixed", "Combined Type Osteosarcoma", "combined type osteosarcoma", "mixed cell type osteosarcoma", "mixed type osteogenic sarcoma", "mixed cell type osteogenic sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mixed osteosarcoma", "shortest_name_length": 18}
{"curie": "MONDO:0020074", "names": ["PME", "Myoclonus seizures", "Generalised myoclonic seizure", "Generalized myoclonic seizure", "Generalised myoclonic seizures", "progressive myoclonus epilepsy", "Generalized myoclonic seizures", "progressive myoclonic epilepsy", "Progressive Myoclonic Epilepsy", "Progressive myoclonic epilepsy", "Progressive Myoclonus Epilepsy", "Progressive myoclonus epilepsy", "MYOCLONIC EPILEPSY, PROGRESSIVE", "Myoclonic epilepsy, progressive", "Epilepsy, Progressive Myoclonus", "Generalised epileptic myoclonus", "epilepsy, progressive myoclonic", "Epilepsy, progressive myoclonic", "Generalized epileptic myoclonus", "Myoclonic Epilepsy, Progressive", "Epilepsy, Progressive Myoclonic", "progressive myoclonus epilepsies", "Progressive Myoclonus Epilepsies", "Progressive Myoclonic Epilepsies", "Epilepsies, Progressive Myoclonus", "Myoclonic Epilepsies, Progressive", "Epilepsies, Progressive Myoclonic", "Myoclonus Epilepsies, Progressive", "Seizures, myoclonic and generalized", "familial progressive myoclonic epilepsy", "Progressive myoclonic epilepsy (disorder)", "Progressive myoclonic epilepsy (diagnosis)", "Generalized onset myoclonic epileptic seizure", "Generalized-onset myoclonic epileptic seizure", "Generalised-onset myoclonic epileptic seizure", "Generalised onset myoclonic epileptic seizure", "progressive myoclonic epilepsy (disorder) [ambiguous]", "Generalized onset myoclonic epileptic seizure (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive myoclonus epilepsy", "shortest_name_length": 3}
{"curie": "UMLS:C5239117", "names": ["Refractory HER2-Negative Breast Carcinoma", "Refractory HER2 Negative Breast Carcinoma", "Refractory HER2 Negative Breast Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory HER2-Negative Breast Carcinoma", "shortest_name_length": 41}
{"curie": "UMLS:C0566951", "names": ["sore vaginal", "vaginal sore", "vagina ulcer", "ulcer vagina", "Ulcer, vagina", "VAGINAL ULCER", "sores vaginal", "vaginal ulcer", "vagina; ulcer", "ulcer; vagina", "Vaginal ulcer", "vaginal sores", "ulcer vaginal", "ulcers vaginal", "Ulcer of vagina", "vaginal ulceration", "VAGINAL ULCERATION", "Vaginal ulceration", "ulcerations vaginal", "Ulceration of vagina", "Vaginal ulcer (disorder)", "vaginal ulcer (diagnosis)", "vaginal ulcer (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal ulcer", "shortest_name_length": 12}
{"curie": "UMLS:C4524523", "names": ["Stage III", "Stage III Head and Neck Squamous Cell Cancer", "Stage III Cutaneous Squamous Cell Carcinoma of the Head and Neck AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Cutaneous Squamous Cell Carcinoma of the Head and Neck AJCC v8", "shortest_name_length": 9}
{"curie": "UMLS:C1709872", "names": ["Relapsed Adrenal Gland Chromaffinoma", "Recurrent Adrenal Gland Chromaffinoma", "Relapsed Adrenal Gland Pheochromocytoma", "Relapsed Adrenal Gland Chromaffin Tumor", "Recurrent Adrenal Gland Chromaffin Tumor", "Recurrent Adrenal Gland Pheochromocytoma", "Relapsed Adrenal Gland Chromaffin Neoplasm", "Recurrent Adrenal Gland Chromaffin Neoplasm", "Relapsed Adrenal Gland Chromaffin Paraganglioma", "Recurrent Adrenal Gland Chromaffin Paraganglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Adrenal Gland Pheochromocytoma", "shortest_name_length": 36}
{"curie": "UMLS:C0877613", "names": ["rectal cramps", "Rectal cramps", "cramping rectal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rectal cramps", "shortest_name_length": 13}
{"curie": "UMLS:C4525859", "names": ["Rectal Neuroendocrine Tumor by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rectal Neuroendocrine Tumor by AJCC v8 Stage", "shortest_name_length": 44}
{"curie": "MONDO:0002146", "names": ["Hypogonadism", "hypogonadism", "HYPOGONADISM", "Hypogonadotropism", "Hypogonadism, NOS", "hypogonadotropism", "Gonadotropin Deficiency", "Hypogonadism (disorder)", "gonadotropin deficiency", "hypogonadism (diagnosis)", "Decreased activity of gonads"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadism", "shortest_name_length": 12}
{"curie": "UMLS:C4521617", "names": ["Stage IIA Bone Cancer", "Stage IIA Bone Cancer AJCC v8", "Stage IIA Appendicular Skeleton, Trunk, Skull, and Facial Bones Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Bone Cancer AJCC v8", "shortest_name_length": 21}
{"curie": "DOID:0112124", "names": ["RPSRDF", "primary ciliary dyskinesia-retinitis pigmentosa syndrome", "X-linked retinitis pigmentosa and sinorespiratory infections", "RETINITIS PIGMENTOSA, X-LINKED, AND SINORESPIRATORY INFECTIONS WITH OR WITHOUT DEAFNESS", "Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked retinitis pigmentosa and sinorespiratory infections", "shortest_name_length": 6}
{"curie": "MONDO:0003290", "names": ["simple partial epilepsy", "Partial epilepsy, without mention of impairment of consciousness, with intractable epilepsy", "Localization-related (focal) (partial) epilepsy and epileptic syndromes with simple partial seizures, with intractable epilepsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "simple partial epilepsy", "shortest_name_length": 23}
{"curie": "MONDO:0007501", "names": ["PAFC", "Pafc", "Ear Pit", "Ear pit", "Ear Pits", "EAR PITS", "Ear pits", "Ear Dimple", "Preauricular pit", "preauricular pit", "pits preauricular", "Preauricular pits", "Preauricular sinus", "Preauricular Sinus", "preauricular sinus", "Preauricular dimple", "sinus; preauricular", "preauricular; sinus", "Preauricular earpits", "Preauricular dimples", "Dimple, preauricular", "Periauricular Dimple", "fistula preauricular", "Preauricular fistula", "preauricular fistula", "fistula; preauricular", "Preauricular fistulas", "preauricular; fistula", "Fistula auris congenita", "Pit in front of the ear", "Congenital preauricular pit", "Congenital pit, preauricular", "Congenital auricular fistula", "Congenital preauricular sinus", "Pre-auricular sinus congenital", "Preauricular dimple (disorder)", "preauricular sinus (diagnosis)", "Congenital preauricular fistula", "Preauricular fistula (disorder)", "preauricular fistula (diagnosis)", "preauricular fistulae, congenital", "PREAURICULAR FISTULAE, CONGENITAL", "Preauricular Fistulae, Congenital", "Preauricular sinus (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "preauricular fistulae, congenital", "shortest_name_length": 4}
{"curie": "UMLS:C4049249", "names": ["Rebound eczema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rebound eczema", "shortest_name_length": 14}
{"curie": "UMLS:C0345522", "names": ["Base of Tongue Tumor", "Posterior Tongue Tumor", "Tumor of base of tongue", "Base of Tongue Neoplasm", "Tumor of Base of Tongue", "Base of the Tongue Tumor", "Tumour of base of tongue", "Posterior Tongue Neoplasm", "Tumor of Posterior Tongue", "Neoplasm of Base of Tongue", "Neoplasm of base of tongue", "neoplasm of base of tongue", "Base of the Tongue Neoplasm", "Neoplasm of Posterior Tongue", "Tumor of the Posterior Tongue", "Tumor of the Base of the Tongue", "Neoplasm of the Posterior Tongue", "Neoplasm of the Base of the Tongue", "neoplasm of posterior base of tongue", "Neoplasm of base of tongue (disorder)", "neoplasm of base of tongue (diagnosis)", "neoplasm of posterior base of tongue (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Posterior Tongue Neoplasm", "shortest_name_length": 20}
{"curie": "MONDO:0007033", "names": ["abducens palsy", "VI nerve palsy", "6th nerve palsy", "Sixth nerve palsy", "sixth nerve palsy", "VIth nerve disorder", "VIth Nerve Paralysis", "abducens nerve palsy", "VIth nerve paralysis", "VIth nerve Paralysis", "sixth nerve paralysis", "Sixth Nerve Paralysis", "Cranial nerve palsy VI", "Cranial Nerve VI Palsy", "cranial nerve VI palsy", "abducens nerve disease", "Abducens nerve weakness", "abducens nerve weakness", "abducent nerve paralysis", "Abducens Nerve Paralysis", "cranial mononeuropathy VI", "sixth cranial nerve palsy", "disorder of abducent nerve", "sixth cranial nerve disorder", "Sixth cranial nerve disorder", "sixth or abducens nerve palsy", "abducens nerve cranial nerve palsy", "cranial nerve palsy of abducens nerve", "lateral rectus muscle denervation paresis", "Lateral rectus muscle denervation paresis", "Lateral rectus muscle innervation disorder", "lateral rectus muscle innervation disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "abducens nerve palsy", "shortest_name_length": 14}
{"curie": "UMLS:C0854375", "names": ["mucosal hemorrhage", "Mucosal hemorrhage", "Mucosal haemorrhage", "hemorrhages mucosal", "Mucosa hemorrhage NOS", "Mucosal hemorrhage NOS", "Mucosa haemorrhage NOS", "Mucosal haemorrhage NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mucosal hemorrhage", "shortest_name_length": 18}
{"curie": "MONDO:0014920", "names": ["MDPT3", "MCRPE", "patterned macular dystrophy 3", "MACULAR DYSTROPHY, PATTERNED, 3", "macular dystrophy, patterned, 3", "patterned macular dystrophy type 3", "MAPKAPK3 patterned macular dystrophy", "macular dystrophy, patterned, type 3", "MARTINIQUE CRINKLED RETINAL PIGMENT EPITHELIOPATHY", "Martinique crinkled retinal pigment epitheliopathy", "patterned macular dystrophy caused by mutation in MAPKAPK3", "MCRPE - Martinique crinkled retinal pigment epitheliopathy", "Martinique crinkled retinal pigment epitheliopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "patterned macular dystrophy 3", "shortest_name_length": 5}
{"curie": "UMLS:C0854895", "names": ["Malignant hemangiopericytoma metastatic", "Metastatic Malignant Hemangiopericytoma", "Malignant haemangiopericytoma metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant hemangiopericytoma metastatic", "shortest_name_length": 39}
{"curie": "MONDO:0040998", "names": ["pasteurella multocida", "Pasteurella multocida infection", "Pasteurella; infection, multocida", "infection; Pasteurella, multocida", "Infection by Pasteurella multocida", "infection by Pasteurella multocida", "Pasteurella multocida infectious disease", "Infection caused by Pasteurella multocida", "infection caused by Pasteurella multocida", "Pasteurella multocida infection (diagnosis)", "Infection caused by Pasteurella multocida (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pasteurella multocida infectious disease", "shortest_name_length": 21}
{"curie": "UMLS:C4526722", "names": ["Stage IIIA", "Stage IIIA Lung Cancer", "Stage IIIA Lung Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Lung Cancer AJCC v8", "shortest_name_length": 10}
{"curie": "MONDO:0001590", "names": ["TETRAPLEGIA", "Tetraplegia", "tetraplegia", "Quadriplegia", "QUADRIPLEGIA", "Quadraplegia", "quadriplegia", "QuaDriplegia", "Tetraplegias", "quadraplegia", "QUADRAPLEGIA", "Quadriplegias", "Bilateral Diplegia", "bilateral diplegia", "quadriplegia was seen", "quadriplegia (symptom)", "Quadriplegia (disorder)", "Tetraplegia, unspecified", "paralysis; limb, all four", "Quadriplegia, unspecified", "limb; paralysis, all four", "Paralysis of all four limbs", "quadriplegia (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "quadriplegia", "shortest_name_length": 11}
{"curie": "UMLS:C3272820", "names": ["UC-Associated CRC", "Ulcerative Colitis-Associated Colorectal Carcinoma", "Ulcerative Colitis-Associated Colorectal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ulcerative Colitis-Associated Colorectal Adenocarcinoma", "shortest_name_length": 17}
{"curie": "MONDO:0008880", "names": ["Bowen syndrome", "Bowen syndrome of multiple malformations", "BOWEN SYNDROME OF MULTIPLE MALFORMATIONS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bowen syndrome of multiple malformations", "shortest_name_length": 14}
{"curie": "MONDO:0013808", "names": ["Maffucci", "Kast syndrome", "Kast Syndrome", "MAFFUCCI SYNDROME", "maffucci syndrome", "Maffucci syndrome", "Maffucci Syndrome", "Syndrome, Maffucci", "maffucci's syndrome", "Maffucci's Anomalad", "Maffucci's anomalad", "Maffucci's syndrome", "Chondroplasia angiomatosis", "Chondroplasia Angiomatosis", "hemangioma; chondrodysplasia", "Maffucci syndrome (disorder)", "Maffucci type enchondromatosis", "chondrodysplasia with hemangioma", "Chondrodysplasia with Hemangioma", "Chondrodysplasia with hemangioma", "dyschondroplasia with hemangiomas", "Chondrodysplasia with haemangioma", "chondrodysplasia; with hemangioma", "enchondromatosis with hemangiomata", "Enchondromatosis with hemangiomata", "Enchondromatosis with Hemangiomata", "Hemangiomata with dyschondroplasia", "Hemangiomatosis Chondrodystrophica", "hemangiomata with Dyschondroplasia", "hemangiomatosis Chondrodystrophica", "Hemangiomata with Dyschondroplasia", "Haemangiomata with dyschondroplasia", "Enchondromatosis with haemangiomata", "multiple Angiomas and Endochondromas", "Dyschondrodysplasia with hemangiomas", "Dyschondrodysplasia with Hemangiomas", "Multiple Angiomas and Endochondromas", "MULTIPLE ENCHONDROMATOSIS, MAFFUCCI TYPE", "multiple enchondromatosis, Maffucci type", "Dyschondroplasia and Cavernous Hemangioma", "Dyschondroplasia and cavernous hemangioma", "Dyschondroplasia and cavernous haemangioma", "dyschondroplasia with hemangiomas (diagnosis)", "Enchondromatosis with Multiple Cavernous Hemangiomas", "enchondromatosis with multiple cavernous hemangiomas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Maffucci syndrome", "shortest_name_length": 8}
{"curie": "MONDO:0022883", "names": ["craniofacial and skeletal defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniofacial and skeletal defects", "shortest_name_length": 33}
{"curie": "UMLS:C1336958", "names": ["Very Low Risk Esophageal Gastrointestinal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Very Low Risk Esophageal Gastrointestinal Stromal Tumor", "shortest_name_length": 55}
{"curie": "MONDO:0002037", "names": ["PLEURAL", "pleura disease", "pleural disease", "Pleural Disease", "pleural diseases", "Pleural disorder", "pleural disorder", "Pleural Diseases", "Pleura--Diseases", "Disease, Pleural", "PLEURAL DISORDER", "Pleural Disorder", "Pleural Disorders", "disease of pleura", "Pleural disorders", "Diseases, Pleural", "pleural disorders", "disorder of pleura", "Disorder of pleura", "Pleural disorder NOS", "Pleural disorder, NOS", "Disease of pleura, NOS", "DISEASES OF THE PLEURA", "pleura disease or disorder", "disorders of thoracic pleura", "Disorder of pleura (disorder)", "disease (or disorder); pleura", "disease or disorder of pleura", "non-neoplastic pleural disease", "disorders of thoracic pleura (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pleural disorder", "shortest_name_length": 7}
{"curie": "MONDO:0010855", "names": ["stale", "STALE", "Lopes Gorlin syndrome", "Lopes-Gorlin syndrome", "Short tarsus absence of lower eyelashes", "short tarsus absence of lower eyelashes", "Short Tarsus with Absence of Lower Eyelashes", "SHORT TARSUS WITH ABSENCE OF LOWER EYELASHES", "short tarsus with absence of LOWER eyelashes", "Short tarsus-absence of lower eyelashes syndrome", "short tarsus-absence of lower eyelashes syndrome", "Short tarsus with absence of lower eyelashes syndrome", "Short tarsus with absence of lower eyelashes syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short tarsus-absence of lower eyelashes syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C1167782", "names": ["Lung Overinflation", "Lung hyperinflation", "hyperinflation lung", "lung hyperinflation", "hyperinflation lungs", "Overinflation of lung", "Overinflation of Lung", "Hyperinflation of lung", "Pulmonary hyperinflation", "Hyperinflation of lung (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung hyperinflation", "shortest_name_length": 18}
{"curie": "MONDO:0019948", "names": ["Reducing-body myopathy", "reducing body myopathy", "Reducing body myopathy", "reducing body myopathy 1A", "Reducing-body myopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "reducing body myopathy", "shortest_name_length": 22}
{"curie": "UMLS:C1336474", "names": ["Ovarian Yolk Sac Tumor Stage I", "Stage I Ovarian Yolk Sac Tumor", "Yolk Sac Tumor of Ovary Stage I", "Yolk Sac Tumor of the Ovary Stage I", "Stage I Ovarian Yolk Sac Tumor AJCC v7", "Stage I Ovarian Yolk Sac Tumor AJCC v6", "Stage I Ovarian Yolk Sac Tumor AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Ovarian Yolk Sac Tumor AJCC v6 and v7", "shortest_name_length": 30}
{"curie": "UMLS:C1112210", "names": ["Catheter site infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Catheter site infection", "shortest_name_length": 23}
{"curie": "MONDO:0008058", "names": ["cylindrical spirals myopathy", "Cylindrical spirals myopathy", "Cylindrical spirals myopathy (disorder)", "Cylindrical spirals myopathy (diagnosis)", "MYOTONIC MYOPATHY WITH CYLINDRICAL SPIRALS", "Myotonic Myopathy with Cylindrical Spirals", "myotonic myopathy with cylindrical spirals", "congenital anomaly of skeletal muscle cylindrical spirals myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cylindrical spirals myopathy", "shortest_name_length": 28}
{"curie": "MONDO:0003487", "names": ["adenoacanthoma", "Adenoacanthoma", "ADENOACANTHOMA, MALIGNANT", "adenoid squamous carcinoma", "Adenoid Squamous Carcinoma", "Adenoid squamous cell carcinoma", "Adenoid Squamous Cell Carcinoma", "adenoid squamous cell carcinoma", "Squamous cell carcinoma, adenoid", "squamous cell carcinoma of adenoid", "Pseudoglandular Squamous Carcinoma", "Pseudoglandular squamous carcinoma", "pseudoglandular squamous carcinoma", "pseudoglandular epidermoid carcinoma", "Acantholytic squamous cell carcinoma", "acantholytic squamous cell carcinoma", "Pseudoglandular Epidermoid Carcinoma", "Squamous cell carcinoma, acantholytic", "pseudoglandular squamous cell carcinoma", "Pseudoglandular Squamous Cell Carcinoma", "adenocarcinoma with squamous metaplasia", "Adenocarcinoma with Squamous Metaplasia", "Adenocarcinoma with squamous metaplasia", "Pseudoglandular squamous cell carcinoma", "Squamous cell carcinoma, pseudoglandular", "pharyngeal tonsil squamous cell carcinoma", "Pseudoglandular Epidermoid Cell Carcinoma", "pseudoglandular epidermoid cell carcinoma", "adenoid squamous cell carcinoma (diagnosis)", "squamous cell carcinoma of adenoid (diagnosis)", "Acantholytic squamous cell carcinoma (disorder)", "Acantholytic squamous cell carcinoma (diagnosis)", "adenocarcinoma with squamous metaplasia (diagnosis)", "malignant neoplasm carcinoma squamous cell acantholytic", "adenoid squamous cell carcinoma (morphologic abnormality)", "Adenoid squamous cell carcinoma (morphologic abnormality)", "adenocarcinoma with squamous metaplasia (morphologic abnormality)", "Adenocarcinoma with squamous metaplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudoglandular squamous cell carcinoma", "shortest_name_length": 14}
{"curie": "UMLS:C1328353", "names": ["Infective spondylitis", "infectious; spondylitis", "spondylitis; infectious", "spine or vertebra; arthritis, infectious or infective", "arthritis; spine or vertebra, infectious or infective"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infective spondylitis", "shortest_name_length": 21}
{"curie": "MONDO:0011575", "names": ["CEREBROOCULONASAL SYNDROME", "Cerebrooculonasal syndrome", "cerebrooculonasal syndrome", "Cerebrooculonasal Syndrome", "cerebro-oculo-nasal syndrome", "Cerebro-oculo-nasal syndrome", "Cerebrooculonasal syndrome (disorder)", "cerebrooculonasal syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebrooculonasal syndrome", "shortest_name_length": 26}
{"curie": "UMLS:C1390619", "names": ["Bowel Burn", "bowel; burn", "burn; bowel"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bowel Burn", "shortest_name_length": 10}
{"curie": "MONDO:0002864", "names": ["Anal Rhabdomyosarcoma", "anal rhabdomyosarcoma", "anus rhabdomyosarcoma", "Rhabdomyosarcoma of Anus", "rhabdomyosarcoma of anus", "Rhabdomyosarcoma of the Anus", "rhabdomyosarcoma of the anus", "anus rhabdomyosarcoma (disease)", "rhabdomyosarcoma (disease) of anus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anus rhabdomyosarcoma", "shortest_name_length": 21}
{"curie": "MONDO:0023122", "names": ["Familial prostate cancer", "prostate cancer, somatic", "familial prostate cancer", "prostate cancer, familial", "Prostate cancer, familial", "Hereditary prostate cancer", "Hereditary Prostate Cancer", "hereditary prostate cancer", "prostate cancer, hereditary", "familial prostate carcinoma", "hereditary prostate carcinoma", "Hereditary Prostate Carcinoma", "Familial malignant neoplasm of prostate", "Familial malignant neoplasm of prostate (disorder)", "Familial malignant neoplasm of prostate (diagnosis)", "prostate cancer, autosomal dominant, somatic mutation", "prostate cancer, susceptibility to, autosomal dominant, somatic mutation", "prostate cancer, familial, susceptibility to, autosomal dominant, somatic mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial prostate carcinoma", "shortest_name_length": 24}
{"curie": "UMLS:C4288001", "names": ["Vulvar Papillary Hidradenoma", "Vulvar Hidradenoma Papilliferum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Hidradenoma Papilliferum", "shortest_name_length": 28}
{"curie": "UMLS:C0041891", "names": ["transient organic mental disorder", "Transient organic mental disorder", "Transient Organic Mental Disorder", "Transient organic mental disorder (disorder)", "transient organic mental disorder (diagnosis)", "Unspecified transient organic mental disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transient Organic Mental Disorder", "shortest_name_length": 33}
{"curie": "UMLS:C1828336", "names": ["Skull Osteoma", "Osteoma of skull", "Osteoma of skull (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Osteoma of skull", "shortest_name_length": 13}
{"curie": "UMLS:C0596368", "names": ["Congenital Digestive System Disorder", "Gastrointestinal disorder congenital", "congenital gastrointestinal disorder", "Congenital Gastrointestinal Disorder", "Gastrointestinal disorder congenital NOS", "Congenital Abnormality of the Digestive System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal disorder congenital", "shortest_name_length": 36}
{"curie": "UMLS:C0677690", "names": ["Stage II Diffuse Small Cleaved Cell Lymphoma", "contiguous stage II adult diffuse small cleaved cell lymphoma", "Contiguous Stage II Adult Diffuse Small Cleaved Cell Lymphoma", "Stage II Contiguous Adult Diffuse Small Cleaved Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Contiguous Adult Diffuse Small Cleaved Cell Lymphoma", "shortest_name_length": 44}
{"curie": "MONDO:0005772", "names": ["Geotrichosis", "GEOTRICHOSIS", "Geotrichoses", "geotrichosis", "Geotrichum infection", "Geotrichum; infection", "infection; Geotrichum", "Infection by Geotrichum", "Geotrichosis (disorder)", "geotrichosis (diagnosis)", "Infection by Geotrichum, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "geotrichosis", "shortest_name_length": 12}
{"curie": "UMLS:C0264955", "names": ["Idiopathic arterial calcification of infancy", "Idiopathic arterial calcification of infancy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Idiopathic arterial calcification of infancy", "shortest_name_length": 44}
{"curie": "UMLS:C0241266", "names": ["SUBCUTANEOUS ABSCESS", "subcutaneous abscess", "abscess subcutaneous", "Subcutaneous abscess", "Subcutaneous Abscess", "abscesses subcutaneous", "subcutaneous abscess (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subcutaneous Abscess", "shortest_name_length": 20}
{"curie": "UMLS:C4552019", "names": ["Stage IS", "stage IS cancer of testis", "Stage IS Cancer of Testis", "stage IS testicular cancer", "Stage IS Testicular Cancer", "Stage IS Cancer of the Testis", "stage IS cancer of the testis", "Stage IS Testicular Cancer AJCC v7", "Stage IS Testicular Cancer AJCC v6", "stage IS testicular cancer AJCC v7", "stage IS testicular cancer AJCC v6", "Stage IS Testicular Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IS Testicular Cancer AJCC v6 and v7", "shortest_name_length": 8}
{"curie": "MONDO:0013443", "names": ["SCKL5", "SECKEL SYNDROME 5", "Seckel syndrome 5", "Seckel syndrome type 5", "CEP152 Seckel syndrome", "Seckel syndrome caused by mutation in CEP152"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Seckel syndrome 5", "shortest_name_length": 5}
{"curie": "MONDO:0006311", "names": ["MDS/MPD", "MPD/MDS", "MPD-MDS", "MDS/MPN", "MDS-MPD", "myelodysplastic myeloproliferative cancer", "myelodysplastic/myeloproliferative disease", "myelodysplastic myeloproliferative disease", "Myelodysplastic/Myeloproliferative Disease", "Myelodysplastic/Myeloproliferative Diseases", "myelodysplastic/myeloproliferative disorder", "myelodysplastic/myeloproliferative neoplasm", "myelodysplastic/myeloproliferative diseases", "Myelodysplastic/Myeloproliferative Disorder", "Myelodysplastic/Myeloproliferative Neoplasm", "Myeloproliferative/Myelodysplastic syndromes", "Myelodysplastic/Myeloproliferative Disorders", "myelodysplastic/myeloproliferative disorders", "myeloproliferative/myelodysplastic syndromes", "myeloproliferative/myelodysplastic disorders", "myelodysplastic/myeloproliferative neoplasms", "Myeloproliferative/Myelodysplastic Disorders", "Myeloproliferative/Myelodysplastic Syndromes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myelodysplastic/myeloproliferative neoplasm", "shortest_name_length": 7}
{"curie": "MONDO:0001500", "names": ["transsexualism", "gender dysphoria", "gender incongruence", "Gender role disorder", "Gender Role Disorders", "Gender-role disorder NOS", "Gender Identity Disorder", "gender identify disorder", "disorder gender identity", "Gender identity disorder", "gender identity disorder", "identity gender disorder", "Gender identity disorders", "gender identity; disorder", "GENDER IDENTITY DISORDERS", "gender identity disorders", "Gender identity disorder NOS", "Gender identity disorder, NOS", "Psychosexual identity disorder", "Sexual orientation disturbance", "psychosexual identity disorder", "Disorder;psychosexual identity", "Gender identity disorder (disorder)", "Sexual orientation disturbance, NOS", "gender identity; disorder, childhood", "Gender identity disorder in children", "gender identity disorder (diagnosis)", "Gender identity disorder of childhood", "Gender identity disorder, unspecified", "gender identity disorder of childhood", "Psychosexual identity disorder (disorder)", "psychosexual identity disorder (diagnosis)", "Trans-sexualism with unspecified sexual history", "Gender identity disorder of childhood (disorder)", "gender identity disorder of childhood (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gender identity disorder", "shortest_name_length": 14}
{"curie": "MONDO:0019006", "names": ["SRN1", "Genetic SRNS", "Idiopathic SRNS", "familial idiopathic nephrotic syndrome", "Genetic steroid-resistant nephrotic syndrome", "Hereditary steroid-resistant nephrotic syndrome", "Idiopathic steroid-resistant nephrotic syndrome", "Nephrotic syndrome, idiopathic, steroid-resistant", "Genetic steroid-resistant nephrotic syndrome (disorder)", "familial idiopathic steroid-resistant nephrotic syndrome", "Familial idiopathic steroid-resistant nephrotic syndrome", "NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE", "Nephrotic syndrome, steroid-resistant, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial idiopathic steroid-resistant nephrotic syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C3203547", "names": ["AxSpA", "Axial Spondyloarthritis", "Axial spondyloarthritis", "Spondyloarthritis, Axial", "Axial Spondyloarthritides", "Spondyloarthritides, Axial", "Axial spondyloarthritis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Axial Spondyloarthritis", "shortest_name_length": 5}
{"curie": "UMLS:C1535851", "names": ["Implant site abscess"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Implant site abscess", "shortest_name_length": 20}
{"curie": "UMLS:C0280154", "names": ["low-grade, stage III adult NHL", "adult NHL, stage III, low grade", "NHL, low grade, stage III adult", "Stage III Low Grade Adult Non-Hodgkin's Lymphoma", "non-Hodgkin's lymphoma, low grade, stage III adult", "lymphoma, low grade, stage III adult non-Hodgkin's", "adult non-Hodgkin's lymphoma, low grade, stage III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Low Grade Adult Non-Hodgkin's Lymphoma", "shortest_name_length": 30}
{"curie": "MONDO:0021094", "names": ["immunodeficiency", "Immunodeficiency", "Immune deficiency", "immuno-deficiency", "immunodeficiency disease", "immunodeficiency disorder", "Decreased immune function", "Immunodeficiency Disorder", "Immunodeficiency Syndrome", "immunodeficiency syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency disease", "shortest_name_length": 16}
{"curie": "UMLS:C1336264", "names": ["Paranasal Sinus Cancer Stage III", "Stage III Paranasal Sinus Cancer", "Stage III Paranasal Sinus Carcinoma", "Stage III Accessory Sinus Carcinoma", "Stage III Carcinoma of Accessory Sinus", "Stage III Carcinoma of Paranasal Sinus", "Stage III Paranasal Sinus Cancer AJCC v7", "Stage III Paranasal Sinus Cancer AJCC v6", "Stage III Carcinoma of the Accessory Sinus", "Stage III Carcinoma of the Paranasal Sinus", "Stage III Paranasal Sinus Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Paranasal Sinus Cancer AJCC v6 and v7", "shortest_name_length": 32}
{"curie": "MONDO:0011021", "names": ["NID B", "neuronal intestinal dysplasia type B", "neuronal intestinal dysplasia, type B", "Neuronal Intestinal Dysplasia, Type B", "NEURONAL INTESTINAL DYSPLASIA, TYPE B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuronal intestinal dysplasia, type B", "shortest_name_length": 5}
{"curie": "MONDO:0003236", "names": ["atypical polypoid adenomyoma", "Atypical Polypoid Adenomyoma", "Atypical polypoid adenomyoma", "Atypical polypoid adenomyoma (morphologic abnormality)", "atypical polypoid adenomyoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical polypoid adenomyoma", "shortest_name_length": 28}
{"curie": "MONDO:0000722", "names": ["synpolydactyly", "syndactyly type 2", "isolated synpolydactyly", "nonsyndromic synpolydactyly", "non-syndromic synpolydactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-syndromic synpolydactyly", "shortest_name_length": 14}
{"curie": "MONDO:0018136", "names": ["OCA1-MP", "MP OCA type 1", "Platinum oculocutaneous albinism", "Minimal pigment oculocutaneous albinism", "minimal pigment oculocutaneous albinism type 1", "Minimal pigment oculocutaneous albinism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "minimal pigment oculocutaneous albinism type 1", "shortest_name_length": 7}
{"curie": "UMLS:C0278812", "names": ["recurrent extrahepatic bile duct cancer", "Recurrent Extrahepatic Bile Duct Cancer", "extrahepatic bile duct cancer, recurrent", "bile duct cancer, recurrent extrahepatic", "Relapsed Cancer of Extrahepatic Bile Duct", "Recurrent Extrahepatic Bile Duct Carcinoma", "Recurrent Cancer of Extrahepatic Bile Duct", "Relapsed Cancer of the Extrahepatic Bile Duct", "Recurrent Cancer of the Extrahepatic Bile Duct"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Extrahepatic Bile Duct Carcinoma", "shortest_name_length": 39}
{"curie": "UMLS:C1142075", "names": ["Negative thoughts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Negative thoughts", "shortest_name_length": 17}
{"curie": "UMLS:C4525658", "names": ["Stage III Jejunal Neuroendocrine Tumor", "Stage III Jejunal Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Jejunal Neuroendocrine Tumor AJCC v8", "shortest_name_length": 38}
{"curie": "UMLS:C4553753", "names": ["Stage IV", "Stage IV Renal Cell Cancer", "Stage IV Renal Cell Cancer AJCC v8", "Stage IV Renal Cell Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Renal Cell Cancer AJCC v8", "shortest_name_length": 8}
{"curie": "UMLS:C0156227", "names": ["Nephrotic Syndrome with Lesion of Proliferative Glomerulonephritis", "Nephrotic syndrome with lesion of proliferative glomerulonephritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic syndrome with lesion of proliferative glomerulonephritis", "shortest_name_length": 66}
{"curie": "MONDO:0018894", "names": ["dSMA", "dHMN", "distal spinal muscular atrophy", "Distal spinal muscular atrophy", "Distal Spinal Muscular Atrophy", "spinal muscular atrophy distal", "muscle; atrophy, spinal, distal", "Spinal Muscular Atrophy, Distal", "atrophy; muscle, spinal, distal", "distal hereditary motor neuropathy", "Distal hereditary motor neuropathy", "Distal spinal muscular atrophy (disorder)", "Distal spinal muscular atrophy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal hereditary motor neuropathy", "shortest_name_length": 4}
{"curie": "MONDO:0033926", "names": ["prepubertal anorexia nervosa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prepubertal anorexia nervosa", "shortest_name_length": 28}
{"curie": "UMLS:C0269188", "names": ["uterus cyst", "cyst uterus", "cysts uterus", "uterine cyst", "Cyst;uterine", "cyst; uterus", "uterus; cyst", "UTERINE CYST", "Uterine cyst", "cysts uterine", "cyst of uterus", "Cyst of uterus", "Cyst of uterus (disorder)", "cyst of uterus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cyst of uterus", "shortest_name_length": 11}
{"curie": "UMLS:C1168328", "names": ["LGPIN", "PIN-1", "Grade I PIN", "Grade 1 PIN", "Low-Grade PIN", "Grade 1 Prostatic Intraepithelial Neoplasia", "Grade I Prostatic Intraepithelial Neoplasia", "Low Grade Prostatic Intraepithelial Neoplasia", "Low grade prostatic intraepithelial neoplasia", "low grade prostatic intraepithelial neoplasia", "Low-Grade Intraepithelial Neoplasia of Prostate", "Low-Grade Intraepithelial Neoplasia of the Prostate", "Low grade prostatic intraepithelial neoplasia (disorder)", "low grade prostatic intraepithelial neoplasia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Grade Prostatic Intraepithelial Neoplasia", "shortest_name_length": 5}
{"curie": "UMLS:C2931337", "names": ["del(3p25)", "Monosomy 3p25", "Deletion 3p25", "Chromosome 3, monosomy 3p25"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chromosome 3, monosomy 3p25", "shortest_name_length": 9}
{"curie": "UMLS:C3899641", "names": ["Childhood Small Cell Lung Cancer", "Childhood Lung Small Cell Carcinoma", "Childhood Small Cell Lung Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Lung Small Cell Carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0003281", "names": ["ovary cystic teratoma", "ovarian cystic teratoma", "Ovarian Cystic Teratoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian cystic teratoma", "shortest_name_length": 21}
{"curie": "MONDO:0011436", "names": ["HMN6", "Hmn6", "Dhmn6", "dSMA1", "Dsma1", "Hmnvi", "HMN 6", "DSMA1", "dHMN6", "DHMN6", "SMARD1", "SIANRF", "Sianrf", "Smard1", "HMN VI", "distal-HMN type 6", "Distal-HMN type 6", "IGHMBP2 spinal muscular atrophy", "distal spinal muscular atrophy 1", "Diaphragmatic spinal muscular atrophy", "Diaphragmatic Spinal Muscular Atrophy", "diaphragmatic spinal muscular atrophy", "Distal Spinal Muscular Atrophy Type 1", "Distal spinal muscular atrophy type 1", "SPINAL MUSCULAR ATROPHY, DIAPHRAGMATIC", "spinal muscular atrophy, diaphragmatic", "Spinal Muscular Atrophy, Diaphragmatic", "Distal hereditary motor neuropathy type 6", "distal hereditary motor neuropathy type 6", "Distal Hereditary Motor Neuronopathy Type Vi", "Distal hereditary motor neuronopathy type VI", "neuronopathy, distal hereditary motor, type 6", "Neuronopathy, Distal Hereditary Motor, Type VI", "NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VI", "neuronopathy, distal hereditary motor, type VI", "Spinal muscular atrophy with respiratory distress", "Spinal Muscular Atrophy with Respiratory Distress", "SPINAL MUSCULAR ATROPHY WITH RESPIRATORY DISTRESS 1", "spinal muscular atrophy with respiratory distress 1", "Spinal muscular atrophy with respiratory distress 1", "Autosomal recessive distal spinal muscular atrophy 1", "Autosomal Recessive Distal Spinal Muscular Atrophy 1", "autosomal recessive distal spinal muscular atrophy 1", "spinal muscular atrophy caused by mutation in IGHMBP2", "spinal muscular atrophy, distal, autosomal recessive, 1", "SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1", "Spinal Muscular Atrophy, Distal, Autosomal Recessive, 1", "Spinal Muscular Atrophy with Respiratory Distress Type 1", "Spinal muscular atrophy with respiratory distress type 1", "spinal muscular atrophy with respiratory distress type 1", "autosomal recessive distal spinal muscular atrophy type 1", "Autosomal recessive distal spinal muscular atrophy type 1", "SEVERE INFANTILE AXONAL NEUROPATHY WITH RESPIRATORY FAILURE", "severe infantile axonal neuropathy with respiratory failure", "Severe Infantile Axonal Neuropathy With Respiratory Failure", "Severe infantile axonal neuropathy with respiratory failure", "spinal muscular atrophy, distal, autosomal recessive, type 1", "Neuronopathy, Severe Infantile Axonal, With Respiratory Failure", "neuronopathy, Severe infantile axonal, with respiratory failure", "NEURONOPATHY, SEVERE INFANTILE AXONAL, WITH RESPIRATORY FAILURE", "severe infantile axonal neuropathy with respiratory failure type 1", "Severe infantile axonal neuropathy with respiratory failure type 1", "Spinal muscular atrophy with respiratory distress type 1 (disorder)", "Autosomal recessive spinal muscular atrophy with respiratory distress", "autosomal recessive spinal muscular atrophy with respiratory distress"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive distal spinal muscular atrophy 1", "shortest_name_length": 4}
{"curie": "MONDO:0015474", "names": ["Crypto", "cryptosporidiosis", "Cryptosporidiasis", "cryptosporidiasis", "Cryptosporidiosis", "CRYPTOSPORIDIOSIS", "Cryptosporidioses", "Cryptosporidium Infection", "cryptosporidium infection", "Cryptosporidia infections", "Cryptosporidium infection", "Cryptosporidium; infection", "Cryptosporidium Infections", "Infection, Cryptosporidium", "infection; Cryptosporidium", "Cryptosporidiosis infection", "Cryptosporidiosis (disorder)", "Infection by Cryptosporidium", "Intestinal cryptosporidiosis", "intestinal cryptosporidiosis", "infection by Cryptosporidium", "cryptosporidiosis (diagnosis)", "Cryptosporidial gastroenteritis", "Cryptosporidial Gastroenteritis", "Gastroenteritis cryptosporidial", "gastroenteritis cryptosporidial", "Cryptosporidium; gastroenteritis", "gastroenteritis; Cryptosporidium", "Infection by Cryptosporidium, NOS", "Cryptosporidium infectious disease", "Infection caused by Cryptosporidium", "Cryptosporidium disease or disorder", "Cryptosporidial gastroenteritis (disorder)", "Cryptosporidium caused disease or disorder", "Cryptosporidial gastroenteritis (diagnosis)", "Infection caused by Cryptosporidium (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cryptosporidiosis", "shortest_name_length": 6}
{"curie": "MONDO:0023961", "names": ["visceral neuropathy, familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "visceral neuropathy, familial", "shortest_name_length": 29}
{"curie": "UMLS:C0016479", "names": ["FOOD POISONING", "Food poisoning", "Poisoning;food", "food poisoning", "Food Poisoning", "Poisoning, Food", "Food Poisonings", "food; poisoning", "poisoning; food", "Foodborne Illness", "Food poisoning NOS", "food; intoxication", "intoxication; food", "Food poisoning, NOS", "FP - Food poisoning", "Food toxi-infection", "Food poisoning (disorder)", "food poisoning (diagnosis)", "Food poisoning, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Food Poisoning", "shortest_name_length": 14}
{"curie": "UMLS:C0852928", "names": ["Insomnia exacerbated", "Exacerbated Insomnia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Insomnia exacerbated", "shortest_name_length": 20}
{"curie": "MONDO:0013446", "names": ["LCA6", "Leber Congenital Amaurosis 6", "LEBER CONGENITAL AMAUROSIS 6", "Leber congenital amaurosis 6", "Leber congenital amaurosis type 6", "RPGRIP1 Leber congenital amaurosis", "Leber congenital amaurosis caused by mutation in RPGRIP1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leber congenital amaurosis 6", "shortest_name_length": 4}
{"curie": "UMLS:C5670003", "names": ["Non-Hematologic Toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Hematologic Toxicity", "shortest_name_length": 24}
{"curie": "UMLS:C4521874", "names": ["Stage IB", "Stage IB Pancreatic Cancer", "Stage IB Pancreatic Cancer AJCC v8", "Stage IB Exocrine Pancreatic Cancer AJCC v8", "Stage IB Exocrine Pancreatic Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Pancreatic Cancer AJCC v8", "shortest_name_length": 8}
{"curie": "MONDO:0002603", "names": ["Angiomyolipoma", "angiomyolipoma", "angiomyolipomas", "Angiomyolipomas", "Hamartoma of kidney", "Renal angiomyolipoma", "Renal Angiomyolipoma", "renal angiomyolipoma", "angiomyolipoma kidney", "Kidney angiomyolipoma", "kidney angiomyolipoma", "Kidney Angiomyolipoma", "angiomyolipoma kidneys", "KIDNEY, ANGIOMYOLIPOMA", "Angiomyolipoma of kidney", "Angiomyolipoma of Kidney", "angiomyolipoma of kidney", "angiomyolipoma of the kidney", "Angiomyolipoma of the Kidney", "Angiomyolipoma of kidney (disorder)", "angiomyolipoma of kidney (diagnosis)", "angiomyolipoma (morphologic abnormality)", "Angiomyolipoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angiomyolipoma", "shortest_name_length": 14}
{"curie": "UMLS:C1334369", "names": ["Larynx Carcinoid Tumor", "Laryngeal Carcinoid Tumor", "Carcinoid Tumor of Larynx", "Carcinoid Tumor of the Larynx"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laryngeal Carcinoid Tumor", "shortest_name_length": 22}
{"curie": "MONDO:0001062", "names": ["pyloric antrum cancer", "cancer of pyloric antrum", "malignant pyloric antrum neoplasm", "malignant tumor of pyloric antrum", "Malignant tumor of pyloric antrum", "Malignant tumour of pyloric antrum", "Malignant neoplasm of pyloric antrum", "malignant neoplasm of pyloric antrum", "malignant neoplasm of antrum of stomach", "Malignant neoplasm of antrum of stomach NOS", "Malignant tumor of pyloric antrum (disorder)", "malignant tumor of pyloric antrum of stomach", "Malignant neoplasm of pyloric antrum of stomach", "malignant neoplasm of pyloric antrum of stomach", "malignant neoplasm of pyloric antrum of stomach (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyloric antrum cancer", "shortest_name_length": 21}
{"curie": "MONDO:0001142", "names": ["sialoadenopathy", "salivary disorder", "disorders salivary", "Sialoadenopathy NOS", "Salivary gland disease", "salivary gland disease", "Salivary Gland Problem", "SALIVARY GLAND DISEASE", "Salivary Gland Disease", "Salivary Gland Disorder", "salivary gland diseases", "diseases gland salivary", "Salivary Gland Diseases", "salivary gland disorder", "salivary gland; disease", "Gland Disease, Salivary", "Disease, Salivary Gland", "Salivary gland disorder", "Diseases, Salivary Gland", "Salivary Gland Disorders", "Gland Diseases, Salivary", "salivary glands diseases", "disorders gland salivary", "disorder glands salivary", "Salivary glands--Diseases", "disorders glands salivary", "Disease of salivary glands", "SALIVARY GLAND ABNORMALITY", "Disorder of salivary gland", "Diseases of salivary glands", "Salivary gland disorder NOS", "Disease of salivary gland, NOS", "saliva-secreting gland disease", "DISEASES OF THE SALIVARY GLANDS", "Diseases of the salivary glands", "disease disorders gland salivary", "disease of saliva-secreting gland", "disorder of saliva-secreting gland", "Abnormality of the salivary glands", "Abnormal salivary gland morphology", "salivary gland disorder (diagnosis)", "Non-neoplastic Salivary gland disease", "Disorder of salivary gland (disorder)", "non-neoplastic salivary gland disease", "Disease of salivary gland, unspecified", "Unspecified disease of the salivary glands", "saliva-secreting gland disease or disorder", "disease or disorder of saliva-secreting gland", "Other specified diseases of the salivary glands"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "salivary gland disorder", "shortest_name_length": 15}
{"curie": "MONDO:0001832", "names": ["Esophagitis bacterial", "bacterial esophagitis", "Bacterial esophagitis", "Bacterial Esophagitis", "Bacterial oesophagitis", "Oesophagitis bacterial", "Esophagitis bacterial NOS", "Oesophagitis bacterial NOS", "Bacterial esophagitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bacterial esophagitis", "shortest_name_length": 21}
{"curie": "UMLS:C4683582", "names": ["Lugano Classification Stage III Adult Non-Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage III Adult Non-Hodgkin Lymphoma AJCC v8", "shortest_name_length": 66}
{"curie": "UMLS:C4054361", "names": ["Nephrotic Syndrome - WT1 Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - WT1 Associated", "shortest_name_length": 35}
{"curie": "MONDO:0013916", "names": ["NPHP14", "JBTS19", "NEPHRONOPHTHISIS 14", "Joubert syndrome 19", "JOUBERT SYNDROME 19", "nephronophthisis 14", "nephronophthisis type 14", "ZNF423 nephronophthisis (disease)", "nephronophthisis (disease) caused by mutation in ZNF423"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephronophthisis 14", "shortest_name_length": 6}
{"curie": "MONDO:0002713", "names": ["epidural tumor", "Epidural tumor", "Epidural Tumor", "epidural tumors", "Epidural tumour", "Epidural Tumors", "Extradural Tumor", "Extradural tumor", "extradural tumor", "epidural neoplasm", "Epidural Neoplasm", "Epidural Neoplasms", "Extradural Neoplasm", "extradural neoplasm", "Extradural neoplasm", "Neoplasms, Epidural", "epidural space tumor", "epidural spinal tumors", "Epidural Spinal Tumors", "tumor of epidural space", "epidural space neoplasm", "Extradural Spinal Tumors", "extradural spinal tumors", "Epidural Spinal Neoplasms", "epidural spinal neoplasms", "neoplasm of epidural space", "Neoplasm of epidural space", "Extradural Spinal Neoplasms", "Epidural Spinal Canal Tumor", "epidural spinal canal tumor", "extradural spinal neoplasms", "Neoplasm of extradural space", "Epidural Spinal Canal Tumors", "epidural spinal canal tumors", "extradural spinal canal tumor", "Extradural Spinal Canal Tumor", "epidural spinal canal neoplasm", "Tumor of Epidural Spinal Canal", "Epidural Spinal Canal Neoplasm", "tumor of epidural spinal canal", "tumor of extradural spinal canal", "Extradural Spinal Canal Neoplasm", "extradural spinal canal neoplasm", "Tumor of Extradural Spinal Canal", "neoplasm of epidural spinal canal", "Extradural Spinal Canal Neoplasms", "extradural spinal canal neoplasms", "Neoplasm of Epidural Spinal Canal", "Tumor of the Epidural Spinal Canal", "tumor of the epidural spinal canal", "Neoplasm of Extradural Spinal Canal", "neoplasm of extradural spinal canal", "tumor of the extradural spinal canal", "Tumor of the Extradural Spinal Canal", "Neoplasm of epidural space (disorder)", "neoplasm of the epidural spinal canal", "Neoplasm of the Epidural Spinal Canal", "Neoplasm of the Extradural Spinal Canal", "neoplasm of the extradural spinal canal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidural spinal canal neoplasm", "shortest_name_length": 14}
{"curie": "MONDO:0006514", "names": ["recalcitrant atopic dermatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "recalcitrant atopic dermatitis", "shortest_name_length": 30}
{"curie": "MONDO:0700141", "names": ["Canine Melanoma", "canine melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canine melanoma", "shortest_name_length": 15}
{"curie": "UMLS:C4331337", "names": ["Stage IVA Lip and Oral Cavity Cancer", "Stage IVA Lip and Oral Cavity Cancer AJCC v8", "Stage IVA Lip and Oral Cavity Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Lip and Oral Cavity Cancer AJCC v8", "shortest_name_length": 36}
{"curie": "UMLS:C4682809", "names": ["Stage IIIC Testicular Cancer", "Stage IIIC Testicular Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Testicular Cancer AJCC v8", "shortest_name_length": 28}
{"curie": "UMLS:C0042139", "names": ["uterus perforation", "perforation uterus", "Uterus Perforation", "Uterine perforation", "perforation uterine", "UTERINE PERFORATION", "Perforation uterine", "PERFORATION UTERINE", "Uterine Perforation", "uterine perforation", "Perforation, Uterine", "Uterine Perforations", "Perforations, Uterine", "Perforation of uterus", "perforation of uterus", "Uterus Wall Perforation", "Uterine perforation, NOS", "Perforation of uterus, NOS", "Perforation of uterus (disorder)", "perforation of uterus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Perforation", "shortest_name_length": 18}
{"curie": "MONDO:0800063", "names": ["primordial dwarfism and slender bone disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primordial dwarfism and slender bone disorder", "shortest_name_length": 45}
{"curie": "UMLS:C5557564", "names": ["Metastatic Peritoneal Malignant Mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Peritoneal Malignant Mesothelioma", "shortest_name_length": 44}
{"curie": "MONDO:0013806", "names": ["FCTCS", "cutaneous telangiectasia and cancer syndrome, familial", "CUTANEOUS TELANGIECTASIA AND CANCER SYNDROME, FAMILIAL", "telangiectasia, cutaneous, and cancer syndrome, familial", "TELANGIECTASIA, CUTANEOUS, AND CANCER SYNDROME, FAMILIAL", "familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome", "familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0019503", "names": ["ASOD", "ASGD", "ASMD", "Anterior segment dysgenesis", "anterior segment dysgenesis", "Anterior chamber malformation", "Anterior chamber cleavage defect", "Anterior chamber cleavage disorder", "anterior segment ocular dysgenesis", "Ocular anterior segment dysgenesis", "Anterior segment ocular dysgenesis", "Anterior chamber mesodermal anomalies", "Anterior segment mesencyhmal dysgenesis", "anterior segment mesenchymal dysgenesis", "Anterior segment developmental abnormality", "familial ocular anterior segment mesenchymal dysgenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anterior segment dysgenesis", "shortest_name_length": 4}
{"curie": "MONDO:0012454", "names": ["BMFS7", "AMEDS", "AMeDS", "AMeD Syndrome", "AMeD syndrome", "alcohol intolerance", "AMED SYNDROME, DIGENIC", "acute alcohol sensitivity", "Fanconi Anemia-Like IBMFS", "alcohol sensitivity, acute", "ALCOHOL SENSITIVITY, ACUTE", "HANGOVER, SUSCEPTIBILITY TO", "Hangover, susceptibility to", "HANGOVER, SUSCEPTIBILITY TO (finding)", "ALCOHOL DEPENDENCE, PROTECTION AGAINST", "Bone Marrow Failure Syndrome 7, Digenic", "BONE MARROW FAILURE SYNDROME 7, DIGENIC", "ESOPHAGEAL CANCER, ALCOHOL-RELATED, SUSCEPTIBILITY TO", "Aplastic Anemia, Mental Retardation and Dwarfism Syndrome", "Aplastic anemia-intellectual disability-dwarfism syndrome", "Fanconi Anemia-Like Inherited Bone Marrow Failure Syndrome", "SUBLINGUAL NITROGLYCERIN, SUSCEPTIBILITY TO POOR RESPONSE TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alcohol sensitivity, acute", "shortest_name_length": 5}
{"curie": "UMLS:C4053897", "names": ["Undifferentiated Sarcoma, NOS", "Undifferentiated Sarcoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Undifferentiated Sarcoma, Not Otherwise Specified", "shortest_name_length": 29}
{"curie": "UMLS:C5401300", "names": ["SOC", "Sclerosing Odontogenic Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sclerosing Odontogenic Carcinoma", "shortest_name_length": 3}
{"curie": "MONDO:0021373", "names": ["parietal lobe tumor", "Parietal Lobe Tumor", "Tumor of Parietal Lobe", "Parietal Lobe Neoplasm", "parietal lobe neoplasm", "tumor of parietal lobe", "neoplasm of parietal lobe", "Neoplasm of Parietal Lobe", "Neoplasm of parietal lobe", "Tumor of the Parietal Lobe", "tumor of the parietal lobe", "neoplasm of the parietal lobe", "Neoplasm of the Parietal Lobe", "parietal lobe neoplasm (disease)", "neoplasm of parietal lobe of brain", "Neoplasm of parietal lobe (disorder)", "neoplasm of parietal lobe of brain (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplasm of parietal lobe", "shortest_name_length": 19}
{"curie": "MONDO:0020237", "names": ["lens shape anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lens shape anomaly", "shortest_name_length": 18}
{"curie": "UMLS:C0677685", "names": ["Stage II Non-Hodgkin Lymphoma", "contiguous stage II adult non-Hodgkin lymphoma", "Stage II Contiguous Adult Non-Hodgkin Lymphoma", "stage II contiguous adult non-Hodgkin lymphoma", "Contiguous Stage II Adult Non-Hodgkin's Lymphoma", "contiguous adult non-Hodgkin's lymphoma stage II", "stage II contiguous adult non-Hodgkin's lymphoma", "contiguous stage II adult non-Hodgkin's lymphoma", "Adult Contiguous Stage II Non-Hodgkin's Lymphoma", "Stage II Contiguous Adult Non-Hodgkin's Lymphoma", "Contiguous Adult Non-Hodgkin's Lymphoma Stage II", "adult contiguous stage II non-Hodgkin's lymphoma", "Stage II Adult Contiguous Non-Hodgkin's Lymphoma", "stage II adult contiguous non-Hodgkin's lymphoma", "Adult Contiguous Non-Hodgkin's Lymphoma Stage II", "Ann Arbor Stage II Contiguous Adult Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage II Contiguous Adult Non-Hodgkin Lymphoma", "shortest_name_length": 29}
{"curie": "MONDO:0004797", "names": ["leg mononeuritis", "Mononeuritis;legs", "mononeuritis lower limb", "Mononeuritis lower limb", "mononeuritis; lower limb", "mononeuritis of the legs", "lower limb; mononeuritis", "Mononeuritis of lower limb", "mononeuritis of lower limb", "LOWER EXTREMITY MONONEURITIS", "mononeuritis of a lower limb", "hindlimb mononeuritis simplex", "Mononeuritis of lower limb, NOS", "mononeuritis simplex of hindlimb", "limb lower mononeuritis unspecified", "mononeuritis of lower limb (diagnosis)", "Mononeuritis of lower limb, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mononeuritis of lower limb", "shortest_name_length": 16}
{"curie": "MONDO:0010941", "names": ["ENUR2", "nocturnal enuresis, 2", "Enuresis, Nocturnal, 2", "enuresis, nocturnal, 2", "ENURESIS, NOCTURNAL, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nocturnal enuresis, 2", "shortest_name_length": 5}
{"curie": "UMLS:C1332252", "names": ["Ampullary Tubular Adenoma", "Ampulla of Vater Tubular Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ampulla of Vater Tubular Adenoma", "shortest_name_length": 25}
{"curie": "MONDO:0002505", "names": ["Astrocytic Tumor", "astrocytic tumor", "Juvenile astrocytoma", "juvenile astrocytoma", "pediatric astrocytoma", "Pediatric Astrocytic Tumor", "pediatric astrocytic tumor", "Childhood Astrocytic Tumor", "childhood astrocytic tumor", "Childhood Astrocytic Tumour", "childhood astrocytic tumour", "astrocytic tumors, childhood", "Astrocytic Tumors, Childhood", "Childhood Astrocytic Neoplasm", "Pediatric Astrocytic Neoplasm", "childhood astrocytic neoplasm", "astrocytic tumor of childhood", "pediatric astrocytic neoplasm", "astrocytoma; juvenile, unspecified site", "juvenile; astrocytoma, unspecified site", "juvenile astrocytoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood astrocytic tumor", "shortest_name_length": 16}
{"curie": "MONDO:0002765", "names": ["Carcinoma cuniculatum", "Epithelioma cuniculatum", "Plantar verrucous carcinoma", "Plantar Verrucous Carcinoma", "plantar verrucous skin carcinoma", "Plantar Verrucous Skin Carcinoma", "Plantar Verrucous Carcinoma of Skin", "plantar verrucous carcinoma of skin", "Plantar verrucous carcinoma (disorder)", "Plantar Verrucous Carcinoma of the Skin", "plantar verrucous carcinoma of the skin", "plantar part of pes verrucous carcinoma", "Plantar verrucous carcinoma (diagnosis)", "skin neoplasm squamous cell carcinoma foot plantar verrucous"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "plantar verrucous skin carcinoma", "shortest_name_length": 21}
{"curie": "MONDO:0020380", "names": ["SCA", "ADCA", "spinocerebellar ataxia", "autosomal dominant cerebellar ataxia", "cerebellar ataxia, autosomal dominant", "autosomal dominant spinocerebellar ataxia", "Pierre Marie cerebellar ataxia (formerly)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant cerebellar ataxia", "shortest_name_length": 3}
{"curie": "MONDO:0004813", "names": ["tuberculous pneumothorax", "Tuberculous pneumothorax", "pneumothorax; tuberculous", "Tuberculous pneumothorax (disorder)", "tuberculous pneumothorax (diagnosis)", "Tuberculous pneumothorax, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tuberculous pneumothorax", "shortest_name_length": 24}
{"curie": "MONDO:0000402", "names": ["Small Cell NEC", "small cell NEC", "Oat Cell Cancer", "oat cell cancer", "Small Cell Cancer", "small cell cancer", "Oat cell carcinoma", "oat cell carcinoma", "Oat Cell Carcinoma", "small cell carcinoma", "Small Cell Carcinoma", "Carcinoma, Small Cell", "intermediate type SCLC", "SCLC, intermediate type", "Small cell carcinoma, NOS", "small cell car. (extrapulmonary)", "Small Cell Neuroendocrine Carcinoma", "Small cell neuroendocrine carcinoma", "small cell neuroendocrine carcinoma", "small cell carcinoma (extrapulmonary)", "intermediate cell small cell carcinoma", "Small Cell Intermediate Cell Carcinoma", "Small cell carcinoma, intermediate cell", "Small Cell Carcinoma, Intermediate Cell", "small cell carcinoma, intermediate cell", "small cell carcinoma - intermediate cell", "Small cell carcinoma - intermediate cell", "intermediate type small cell lung cancer", "small cell lung cancer, intermediate type", "Small Cell Cancer, Intermediate Cell Type", "lung cancer, intermediate type, small cell", "[M] Small cell carcinoma, intermediate cell", "carcinoma; small cell, with intermediate cell, unspecified site", "small cell; carcinoma, with intermediate cell, unspecified site", "small cell carcinoma, intermediate cell (morphologic abnormality)", "Small cell carcinoma, intermediate cell (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small cell carcinoma", "shortest_name_length": 14}
{"curie": "UMLS:C5238933", "names": ["Metastatic Pleural Malignant Mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Pleural Malignant Mesothelioma", "shortest_name_length": 41}
{"curie": "UMLS:C3897740", "names": ["Recurrent Combined Thymic Carcinoma", "Recurrent Combined Thymic Epithelial Tumor", "Recurrent Composite Thymoma-Thymic Carcinoma", "Recurrent Combined Thymic Epithelial Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Combined Thymic Epithelial Neoplasm", "shortest_name_length": 35}
{"curie": "MONDO:0011759", "names": ["MPS1-HS", "MPS1H/S", "MPSIH/S", "MPS I H-S", "Scheie's syndrome", "HURLER-SCHEIE SYNDROME", "Hurler Scheie Syndrome", "Hurler–Scheie syndrome", "Hurler-Scheie Syndrome", "Hurler-Scheie syndrome", "mucopolysaccharidosis Ih/s", "mucopolysaccharidosis IH/S", "Scheie disease mps type 1s", "Mucopolysaccharidosis IH/S", "mucopolysaccharidosis type I-S", "mucopolysaccharidosis, mps-I-s", "mucopolysaccharidosis type IH/S", "Mucopolysaccharidosis Type Ih S", "MUCOPOLYSACCHARIDOSIS TYPE IH/S", "mucopolysaccharidosis type 1H/S", "Mucopolysaccharidosis type 1H/S", "Mucopolysaccharidosis type IH/S", "mucopolysaccharidosis type Ih/S", "Mucopolysaccharidosis, MPS-I-H/S", "Mucopolysaccharidosis type I-H/S", "Hurler-Scheie disease MPS type 1H/S", "l-iduronidase deficiency, Scheie type", "mucopolysaccharidosis type I mild form", "Mucopolysaccharidosis type I-H/S (disorder)", "L-iduronidase deficiency, Hurler-Scheie type", "mucopolysaccharidosis type 1H/S (Hurler-Scheie)", "mucopolysaccharidosis type 1H/S (Hurler-Scheie) (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hurler-Scheie syndrome", "shortest_name_length": 7}
{"curie": "MONDO:0002035", "names": ["colon lymphoma", "Colon Lymphoma", "lymphoma colon", "colonic lymphoma", "Colonic Lymphoma", "Colonic lymphoma", "lymphoma of colon", "Lymphoma of Colon", "LYMPHOMA OF COLON", "Lymphoma of colon", "Lymphoma of the Colon", "lymphoma of the colon", "Primary Colon Lymphoma", "primary colon lymphoma", "Lymphoma of colon (disorder)", "Lymphoma of colon (diagnosis)", "large intestine neoplasm malignant lymphoma colon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colon lymphoma", "shortest_name_length": 14}
{"curie": "MONDO:0011229", "names": ["EE", "eme", "EPEMA syndrome", "Epema Syndrome", "Ethylmalonic encephalopathy", "ethylmalonic encephalopathy", "Encephalopathy, ethylmalonic", "encephalopathy, ethylmalonic", "ENCEPHALOPATHY, ETHYLMALONIC", "Ethylmalonic encephalopathy (disorder)", "encephalopathy, petechiae, and ethylmalonic aciduria", "Encephalopathy, Petechiae, and Ethylmalonic Aciduria", "syndrome of encephalopathy, petechiae, and ethylmalonic aciduria", "Syndrome of encephalopathy, petechiae, and ethylmalonic aciduria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ethylmalonic encephalopathy", "shortest_name_length": 2}
{"curie": "MONDO:0008799", "names": ["MCOPS3", "AEG syndrome", "Aeg syndrome", "AEG SYNDROME", "AEG Syndrome", "SOX2-related eye disorder", "Sox2 Anophthalmia Syndrome", "Syndromic Microphthalmia 3", "Syndromic microphthalmia 3", "SOX2-related eye disorders", "syndromic microphthalmia 3", "Sox2-Related Eye Disorders", "SOX2 anophthalmia syndrome", "Microphthalmia, Syndromic 3", "microphthalmia, syndromic 3", "MICROPHTHALMIA, SYNDROMIC 3", "Syndromic microphthalmia type 3", "syndromic microphthalmia type 3", "syndromic microphthalmia, type 3", "microphthalmia, syndromic type 3", "SOX2 anophthalmia syndrome (disorder)", "anophthalmia esophageal genital syndrome", "Anophthalmia-Esophageal-Genital Syndrome", "anophthalmia-esophageal-genital syndrome", "ANOPHTHALMIA-ESOPHAGEAL-GENITAL SYNDROME", "Anophthalmia-esophageal-genital syndrome", "AEG - anophthalmia-esophageal-genital syndrome", "microphthalmia and esophageal atresia syndrome", "anophthalmia microphthalmia esophageal atresia", "MICROPHTHALMIA AND ESOPHAGEAL ATRESIA SYNDROME", "Microphthalmia And Esophageal Atresia Syndrome", "anophthalmia clinical with associated anomalies", "anophthalmia, clinical, with associated anomalies", "ANOPHTHALMIA, CLINICAL, WITH ASSOCIATED ANOMALIES", "Anophthalmia, Clinical, With Associated Anomalies", "Anophthalmia/microphthalmia-esophageal atresia syndrome", "anophthalmia/microphthalmia-esophageal atresia syndrome", "OPTIC NERVE HYPOPLASIA AND ABNORMALITIES OF THE CENTRAL NERVOUS SYSTEM", "optic nerve hypoplasia and abnormalities of the central nervous system", "Optic Nerve Hypoplasia and Abnormalities of the Central Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anophthalmia/microphthalmia-esophageal atresia syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C0852885", "names": ["buck", "bucks", "bucked", "bucking", "Bucking"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bucking", "shortest_name_length": 4}
{"curie": "UMLS:C0854987", "names": ["Adenocarcinoma lung stage III", "Stage III Lung Adenocarcinoma", "Lung adenocarcinoma stage III", "Lung Adenocarcinoma Stage III", "Lung Adenocarcinoma, Stage III", "Adenocarcinoma of lung stage III", "Stage III Adenocarcinoma of Lung", "Adenocarcinoma of lung, stage III", "Stage III Adenocarcinoma of the Lung", "Stage III Lung Adenocarcinoma AJCC v7", "Adenocarcinoma of lung, stage III (disorder)", "Finding of adenocarcinoma of lung, stage III", "clinical finding tumor stage adenocarcinoma of lung, stage III", "Finding of adenocarcinoma of lung, stage III (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma of lung, stage III", "shortest_name_length": 29}
{"curie": "MONDO:0010612", "names": ["cerebellum agenesis hydrocephaly", "Hydrocephalus With Cerebellar Agenesis", "HYDROCEPHALUS WITH CEREBELLAR AGENESIS", "hydrocephalus with cerebellar agenesis", "hydrocephaly-cerebellar agenesis syndrome", "X-linked hydrocephalus-cerebellar agenesis-intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hydrocephaly-cerebellar agenesis syndrome", "shortest_name_length": 32}
{"curie": "UMLS:C4725804", "names": ["Recurrent Malignant Neoplasm of Multiple Primary Sites"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Malignant Neoplasm of Multiple Primary Sites", "shortest_name_length": 54}
{"curie": "MONDO:0013160", "names": ["MDDGB2", "congenital muscular dystrophy POMT2-related", "congenital muscular dystrophy-POMT2 related", "MUSCULAR DYSTROPHY, CONGENITAL, POMT2-RELATED", "muscular dystrophy, congenital, Pomt2-related", "muscular dystrophy-dystroglycanopathy type B2", "Congenital Muscular Dystrophy-Dystroglycanopathy with Mental Retardation Type B2", "congenital muscular dystrophy-dystroglycanopathy with mental retardation type B2", "muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 2", "congenital muscular dystrophy-dystroglycanopathy with intellectual disability type B2", "muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B2", "muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B, 2", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH IMPAIRED INTELLECTUAL DEVELOPMENT), TYPE B, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B2", "shortest_name_length": 6}
{"curie": "MONDO:0019846", "names": ["acquired CDI", "acquired central diabetes insipidus", "acquired neurogenic diabetes insipidus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired central diabetes insipidus", "shortest_name_length": 12}
{"curie": "MONDO:0003622", "names": ["Pancreatic Vipoma", "VIPoma of pancreas", "pancreatic VIP producing NET", "Pancreatic VIP Producing NET", "Pancreatic VIP Producing Tumor", "VIPoma of pancreas (diagnosis)", "pancreatic VIP Producing tumor", "pancreatic VIP producing tumor", "pancreatic VIP Producing tumour", "Pancreatic VIP Producing Neoplasm", "pancreatic VIP producing neoplasm", "pancreatic VIP-producing neuroendocrine tumor", "Pancreatic VIP-Producing Neuroendocrine Tumor", "pancreatic vasoactive intestinal peptide producing tumor", "Pancreatic Vasoactive Intestinal Peptide Producing Tumor", "pancreatic vasoactive intestinal peptide producing tumour", "pancreatic vasoactive intestinal peptide producing neoplasm", "Pancreatic Vasoactive Intestinal Peptide Producing Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic vasoactive intestinal peptide producing tumor", "shortest_name_length": 17}
{"curie": "MONDO:0004335", "names": ["git disease", "GI Disorder", "GIT disease", "GIT diseases", "GI disorders", "Disease;digestive", "gastroenteropathy", "Digestive Disease", "Gastroenteropathy", "digestive disease", "digestive diseases", "digestive disorder", "Digestive Diseases", "digestive disorders", "digestive; disorder", "disorder; digestive", "Gastroenteropathy NOS", "digestive disease tract", "digestive tract disease", "Gastrointestinal disease", "Digestive System Disease", "gastrointestinal disease", "digestive diseases tract", "disease gastrointestinal", "Gastrointestinal Disease", "Digestive system disease", "digestive system disease", "GASTROINTESTINAL DISEASE", "alimentary system disease", "Gastrointestinal disorder", "Disease, Gastrointestinal", "digestive system disorder", "Gastrointestinal diseases", "Digestive System Disorder", "gastrointestinal diseases", "Gastrointestinal Disorder", "Disorder gastrointestinal", "Digestive System Diseases", "Gastrointestinal Diseases", "GASTROINTESTINAL DISORDER", "digestive system diseases", "diseases gastrointestinal", "DISORDER GASTROINTESTINAL", "gastrointestinal disorder", "gastro-intestinal disorder", "gastrointestinal disorders", "disorder; gastrointestinal", "Gastrointestinal Disorders", "gastrointestinal; disorder", "Digestive System Disorders", "disorders gastrointestinal", "GASTROINTESTINAL DISORDERS", "Gastrointestinal disorders", "digestive system disorders", "Diseases, Gastrointestinal", "disorders gastro intestinal", "Abnormality of the GI tract", "System Disorders, Digestive", "disease of digestive system", "Disorder of digestive system", "disorder of digestive system", "Disorder of Digestive System", "gastroenteropathy (diagnosis)", "Gastrointestinal disorder NOS", "disease gastrointestinal tract", "GASTRO-INTESTINAL DISORDER NOS", "Gastro-intestinal disorder NOS", "Gastrointestinal disorder, NOS", "stomach or intestinal disorder", "gastrointestinal system disease", "GASTROINTESTINAL DISORDER (NOS)", "Gastrointestinal System Disease", "diseases gastrointestinal tract", "Disease of digestive system, NOS", "gastrointestinal tract disorders", "disorders gastrointestinal tract", "Gastrointestinal System Disorder", "Diseases of the digestive system", "diseases of the digestive system", "DISEASES OF THE DIGESTIVE SYSTEM", "gastrointestinal system disorder", "disease of gastrointestinal tract", "Disorder of gastrointestinal tract", "gastroenterological system disease", "GASTRO-INTESTINAL SYSTEM DISORDERS", "GASTROINTESTINAL DISORDERS: GENERAL", "gastrointestinal disorder diagnosis", "gastroenterological system disorder", "Unspecified Gastrointestinal Problem", "digestive system disease or disorder", "gastrointestinal disorders (diagnosis)", "Gastrointestinal and digestive disorder", "disease (or disorder); gastrointestinal", "disease of digestive system (diagnosis)", "Disorder of digestive system (disorder)", "Disease or syndrome of digestive system", "Disorder of gastrointestinal tract, NOS", "disease (or disorder); digestive system", "disease or disorder of digestive system", "Disease of digestive system, unspecified", "Abnormality of the gastrointestinal tract", "Diseases and Syndromes of Digestive System", "disease (or disorder); gastrointestinal tract", "Disorder of gastrointestinal tract (disorder)", "DISEASES OF THE DIGESTIVE SYSTEM: GENERAL CONDITIONS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "digestive system disorder", "shortest_name_length": 11}
{"curie": "UMLS:C5447475", "names": ["Locally Advanced Lung Small Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Lung Small Cell Carcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0010631", "names": ["IP", "IP2, FORMERLY", "IP2 (formerly)", "Bloch-Sulzberger", "Asboe-Hansen disease", "asboe-hansen disease", "Bloch-Siemens Syndrome", "Incontinentia pigmenti", "INCONTINENTIA PIGMENTI", "Bloch-Siemans syndrome", "incontinentia pigmenti", "Bloch-Siemens syndrome", "bloch-siemens syndrome", "Incontinentia Pigmenti", "incontinentia pigmenti 1", "Bloch-Sulzberger syndrome", "Bloch Sulzberger Syndrome", "Bloch-Sulzberger Syndrome", "BLOCH-SULZBERGER SYNDROME", "Bloch Sulzberger syndrome", "Syndrome, Bloch-Sulzberger", "IP - Incontinentia pigmenti", "incontinentia pigmenti (IP)", "melanosis corii degenerativa", "nevus pigmentosus systematicus", "Incontinentia Pigmenti Syndrome", "bloch-sulzberger melanoblastoma", "Incontinentia pigmenti syndrome", "Incontinentia pigmenti, type II", "incontinentia pigmenti syndrome", "Bloch-Sulzberger melanoblastoma", "Bloch-Siemens-Sulzberger Syndrome", "Siemens-Bloch pigmented dermatosis", "incontinentia pigmenti (diagnosis)", "Incontinentia pigmenti type 2 (formerly)", "Incontinentia pigmenti, type II, formerly", "incontinentia pigmenti, X-linked dominant", "INCONTINENTIA PIGMENTI, TYPE II, FORMERLY", "Incontinentia pigmenti syndrome (disorder)", "Incontinentia pigmenti of Bloch-Sulzberger", "pigmentation; congenital, incontinentia pigmenti", "Incontinentia pigmenti, familial Male-lethal type", "melanoblastosis cutis linearis sive systematisata", "INCONTINENTIA PIGMENTI, FAMILIAL MALE-LETHAL TYPE", "Incontinentia pigmenti, familial male-lethal type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "incontinentia pigmenti", "shortest_name_length": 2}
{"curie": "MONDO:0023143", "names": ["fetal enterovirus syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fetal enterovirus syndrome", "shortest_name_length": 26}
{"curie": "UMLS:C0278763", "names": ["adult IBL lymphoma", "IBL lymphoma, adult", "Immunoblastic Lymphoma", "Adult Immunoblastic Lymphoma", "adult immunoblastic large cell lymphoma", "Adult Immunoblastic Large Cell Lymphoma", "immunoblastic large cell lymphoma, adult", "large cell lymphoma, adult immunoblastic", "lymphoma, immunoblastic large cell, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Immunoblastic Lymphoma", "shortest_name_length": 18}
{"curie": "UMLS:C0854171", "names": ["Temperature regulation disorder", "temperature regulation disorder", "disorder; temperature regulation", "temperature regulation; disorder", "disorders regulation temperature", "disordered regulation temperature", "Temperature regulation disorder NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Temperature regulation disorder", "shortest_name_length": 31}
{"curie": "UMLS:C4054086", "names": ["Refluxing Obstructed Megaureter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refluxing Obstructed Megaureter", "shortest_name_length": 31}
{"curie": "MONDO:0002807", "names": ["bronchus tumor", "bronchus tumour", "Bronchi--Tumors", "Bronchial tumor", "bronchial tumor", "bronchial tumors", "Bronchial tumour", "bronchus neoplasm", "tumor of bronchus", "Tumor of bronchus", "Bronchial Neoplasm", "Bronchial neoplasm", "bronchial neoplasm", "Tumour of bronchus", "Neoplasm, Bronchial", "Bronchial Neoplasms", "Neoplasm of bronchus", "neoplasm of bronchus", "Neoplasms, Bronchial", "bronchial benign neoplasm", "bronchus neoplasm (disease)", "bronchial neoplasm (disease)", "Neoplasm of bronchus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bronchial neoplasm", "shortest_name_length": 14}
{"curie": "MONDO:0008975", "names": ["OSMED", "OSMEDB", "OSMED syndrome", "Nance-Insley syndrome", "NANCE-INSLEY SYNDROME", "Insley-Astley syndrome", "NANCE-SWEENEY CHONDRODYSPLASIA", "Nance-Sweeney chondrodysplasia", "Nance Sweeney chondrodysplasia", "otospondylmegaepiphyseal dysplasia", "otospondylomegaepiphyseal dysplasia", "Otospondylomegaepiphyseal dysplasia", "oto-spondylo-mega-epiphyseal dysplasia", "chondrodystrophy with sensorineural deafness", "CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS", "Otospondylomegaepiphyseal dysplasia (disorder)", "otospondylomegaepiphyseal dysplasia, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "otospondylomegaepiphyseal dysplasia", "shortest_name_length": 5}
{"curie": "UMLS:C1516071", "names": ["Astler-Coller C2 Colon Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Astler-Coller C2 Colon Carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0016711", "names": ["desmoplastic medulloblastoma", "Desmoplastic Medulloblastoma", "Desmoplastic medulloblastoma", "medulloblastoma; desmoplastic", "Desmoplastic Medulloblastomas", "Medulloblastoma, Desmoplastic", "desmoplastic; medulloblastoma", "Medulloblastomas, Desmoplastic", "Desmoplastic nodular medulloblastoma", "Desmoplastic Nodular Medulloblastoma", "desmoplastic nodular medulloblastoma", "Desmoplastic/Nodular Medulloblastoma", "desmoplastic/nodular medulloblastoma", "Desmoplastic/nodular medulloblastoma", "Circumscribed arachnoidal cerebellar sarcoma", "Arachnoidal Cerebellar Sarcoma, Circumscribed", "Sarcoma, Cerebellar, Circumscribed Arachnoidal", "circumscribed; cerebellar sarcoma (arachnoidal)", "sarcoma; cerebellar, circumscribed (arachnoidal)", "cerebellar; sarcoma, circumscribed (arachnoidal)", "Desmoplastic medulloblastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "desmoplastic/nodular medulloblastoma", "shortest_name_length": 28}
{"curie": "MONDO:0008953", "names": ["Zs", "ZS", "ZWS", "CGE", "CG1", "PBD1A", "Cerebrohepatorenal syndrome", "Peroxisome Biogenesis Disorder 1A", "peroxisome biogenesis disorder 1A", "peroxisome biogenesis disorder 1A (Zellweger)", "PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)", "Peroxisome Biogenesis Disorder, Complementation Group E", "PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 1", "Peroxisome Biogenesis Disorder, Complementation Group 1", "PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP E", "peroxisome biogenesis disorder, complementation group E", "peroxisome biogenesis disorder, complementation group 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder 1A (Zellweger)", "shortest_name_length": 2}
{"curie": "MONDO:0012238", "names": ["PEOA2", "autosomal dominant progressive external ophthalmoplegia 2", "progressive external ophthalmoplegia, autosomal dominant 2", "PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL DOMINANT 2", "Progressive External Ophthalmoplegia, Autosomal Dominant, 2", "SLC25A4 progressive external ophthalmoplegia with mitochondrial DNA deletions", "autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2", "PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 2", "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2", "Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2", "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant type 2", "progressive external ophthalmoplegia with mitochondrial DNA deletions caused by mutation in SLC25A4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2", "shortest_name_length": 5}
{"curie": "MONDO:0004961", "names": ["stage I endometrioid carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stage I endometrioid carcinoma", "shortest_name_length": 30}
{"curie": "UMLS:C0740330", "names": ["Genital infection fungal", "GENITAL FUNGAL INFECTION", "fungal genital infection", "genital fungal infection", "fungal genital infections", "fungal genitals infection", "fungal genitals infections", "Genital infection fungal NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Genital infection fungal", "shortest_name_length": 24}
{"curie": "UMLS:C3272657", "names": ["Urethritis Glandularis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urethritis Glandularis", "shortest_name_length": 22}
{"curie": "MONDO:0005087", "names": ["Disease;respiratory", "Respiratory disease", "respiratory disease", "diseases respiratory", "disorder respiratory", "RESPIRATORY DISORDER", "respiratory disorder", "Respiration Disorder", "Respiratory Diseases", "Respiratory Disorder", "Respiratory disorder", "disorders respiratory", "Disorder, Respiration", "respiratory disorders", "respiratory; disorder", "Respiration Disorders", "Disorders, Respiration", "Respiratory disease NOS", "Respiratory disorder NOS", "Respiratory disease other", "Respiratory Tract Disease", "respiratory tract disease", "Respiratory disorder, NOS", "respiratory system disease", "other respiratory disorder", "diseases other respiratory", "Respiratory system disease", "Respiratory Tract Diseases", "Respiratory tract disorder", "Disease, Respiratory Tract", "Respiratory System Disease", "RESPIRATORY DISORDER (NOS)", "respiratory tract diseases", "Respiratory Tract Disorders", "Disease, Respiratory System", "Respiratory system disorder", "respiratory system diseases", "RESPIRATORY SYSTEM DISORDER", "DISORDER RESPIRATORY SYSTEM", "Other respiratory disorders", "respiratory tract disorders", "Respiratory System Disorder", "respiratory system disorder", "Respiratory System Diseases", "RESPIRATORY SYSTEM DISORDERS", "respiratory system disorders", "disease of respiratory system", "RESPIRATORY SYSTEM DISORDER OF", "Disorder of Respiratory System", "disorder of respiratory system", "Disorder of respiratory system", "Unspecified Respiratory Problem", "Other disease respiratory system", "diseases other respiratory system", "respiratory disorders (diagnosis)", "Respiratory disorder, unspecified", "Other respiratory system diseases", "Disease of respiratory system, NOS", "Diseases of the respiratory system", "DISEASES OF THE RESPIRATORY SYSTEM", "disease (or disorder); respiratory", "RESPIRATORY DISEASES: GENERAL TERMS", "Other diseases of respiratory system", "OTHER DISEASES OF RESPIRATORY SYSTEM", "other respiratory disorder (diagnosis)", "respiratory system disease or disorder", "other diseases of the respiratory system", "Other diseases of the respiratory system", "disease or disorder of respiratory system", "Disease or syndrome of respiratory system", "Disorder of respiratory system (disorder)", "Unspecified disease of respiratory system", "Diseases and Syndromes of Respiratory System", "Diseases of the respiratory system (J00-J99)", "Other diseases of the respiratory system (J96-J99)", "Personal history of unspecified disease of respiratory system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "respiratory system disorder", "shortest_name_length": 19}
{"curie": "MONDO:0019615", "names": ["pituitary dermoid and epidermoid cysts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pituitary dermoid and epidermoid cysts", "shortest_name_length": 38}
{"curie": "UMLS:C0346383", "names": ["Fuchs Adenoma", "Fuchs' adenoma", "Coronal Adenoma", "Fuchs' adenoma (disorder)", "Fuchs' adenoma of ciliary body", "Adenomatous Hyperplasia of the Ciliary Body", "Age-Related Hyperplasia of the Ciliary Body", "Age-Related Hyperplasia of the Nonpigmented Ciliary Body Epithelium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fuchs' adenoma", "shortest_name_length": 13}
{"curie": "UMLS:C1735601", "names": ["floppy iris syndrome", "Floppy iris syndrome", "floppy iris syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Floppy iris syndrome", "shortest_name_length": 20}
{"curie": "MONDO:0032820", "names": ["NEDBAF", "neurodevelopmental disorder with structural brain anomalies and dysmorphic facies", "NEURODEVELOPMENTAL DISORDER WITH STRUCTURAL BRAIN ANOMALIES AND DYSMORPHIC FACIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with structural brain anomalies and dysmorphic facies", "shortest_name_length": 6}
{"curie": "UMLS:C1257963", "names": ["Endogenous Hyperinsulinism", "hyperinsulinism endogenous", "Hyperinsulinism, Endogenous", "hyperinsulinism endogenous (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endogenous Hyperinsulinism", "shortest_name_length": 26}
{"curie": "UMLS:C2981348", "names": ["Stage III Lung Cancer", "Stage III Lung Cancer AJCC v6", "Stage III Lung Carcinoma AJCC v6", "Stage III Carcinoma of Lung AJCC v6", "Stage III Carcinoma of the Lung AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Lung Cancer AJCC v6", "shortest_name_length": 21}
{"curie": "MONDO:0019144", "names": ["THPH6", "autosomal recessive thrombophilia due to protein S deficiency", "hereditary thrombophilia due to congenital protein S deficiency", "severe hereditary thrombophilia due to congenital protein S deficiency", "autosomal recessive thrombophilia due to congenital protein S deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary thrombophilia due to congenital protein S deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0003257", "names": ["Pituicyte Tumor", "PITUICYTOMA, benign", "Neurohypophysis tumor", "Neurohypophysis Tumor", "neurohypophysis tumor", "Pituicyte Tumor Family", "neurohypophysis neoplasm", "tumor of neurohypophysis", "Neurohypophysis neoplasm", "Neurohypophysis Neoplasm", "posterior pituitary tumor", "Posterior Pituitary tumor", "Posterior Pituitary Tumor", "neoplasm of neurohypophysis", "posterior pituitary neoplasm", "Posterior Pituitary Neoplasm", "Posterior Pituitary Gland Tumor", "posterior pituitary gland tumor", "Neoplasm of the neurohypophysis", "Posterior Pituitary Gland Neoplasm", "posterior pituitary gland neoplasm", "neurohypophysis neoplasm (disease)", "Neoplasm of the posterior pituitary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "posterior pituitary gland neoplasm", "shortest_name_length": 15}
{"curie": "UMLS:C3829003", "names": ["Mixed Type Pancreatic IPMN", "Mixed Type Pancreatic Intraductal Papillary-Mucinous Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mixed Type Pancreatic Intraductal Papillary-Mucinous Neoplasm", "shortest_name_length": 26}
{"curie": "MONDO:0003232", "names": ["Alcoholic Pancreatitis", "alcoholic pancreatitis", "Alcoholic pancreatitis", "PANCREATITIS ALCOHOLIC", "pancreatitis alcoholic", "Pancreatitis, Alcoholic", "alcohol-induced pancreatitis", "Alcohol-induced pancreatitis", "Inflammation of pancreas due to alcohol", "alcohol-induced pancreatitis (diagnosis)", "Inflammation of pancreas caused by alcohol", "Inflammation of pancreas caused by alcohol (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alcoholic pancreatitis", "shortest_name_length": 22}
{"curie": "MONDO:0100448", "names": ["CORD18", "RAB28 retinopathy", "cone-rod dystrophy 18", "RAB28 cone-rod dystrophy", "RAB28-related retinopathy", "cone-rod dystrophy type 18", "cone-rod dystrophy caused by mutation in RAB28"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "RAB28-related retinopathy", "shortest_name_length": 6}
{"curie": "UMLS:C0860248", "names": ["Fredrickson Type III lipidemia", "Fredrickson Type III Lipidemia", "Fredrickson Type III lipidaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fredrickson Type III lipidaemia", "shortest_name_length": 30}
{"curie": "MONDO:0004873", "names": ["internal piles", "Internal piles", "Internal hemorrhoid", "HEMORRHOID INTERNAL", "internal hemorrhoid", "hemorrhoid internal", "Internal Hemorrhoid", "internal hemorrhoids", "Internal haemorrhoid", "hemorrhoids internal", "Internal hemorrhoids", "internal; hemorrhoids", "Internal haemorrhoids", "hemorrhoids; internal", "Hemorrhoids, internal", "Internal hemorrhoids, NOS", "Internal hemorrhoids (disorder)", "internal hemorrhoids (diagnosis)", "hemorrhoids without complication", "Hemorrhoids without complication", "Haemorrhoids without complication", "internal hemorrhoids (physical finding)", "Hemorrhoids without complication (disorder)", "Unspecified hemorrhoids without complication", "hemorrhoids without complication (diagnosis)", "Unspecified haemorrhoids without complication", "Unspecified hemorrhoids without mention of complication", "Unspecified haemorrhoids without mention of complication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "internal hemorrhoid", "shortest_name_length": 14}
{"curie": "MONDO:0003056", "names": ["lymphoplasmocyte-rich meningioma", "Lymphoplasmacyte-rich meningioma", "Lymphoplasmacyte-Rich Meningioma", "Lymphoplasmocyte-rich meningioma", "lymphoplasmacyte-rich meningioma", "lymphoplasmocyte-rich meningioma (morphologic abnormality)", "Lymphoplasmocyte-rich meningioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphoplasmacyte-rich meningioma", "shortest_name_length": 32}
{"curie": "UMLS:C0086238", "names": ["Secondary generalized epilepsy", "Secondary generalised epilepsy", "Symptomatic generalised epilepsy", "Symptomatic Generalized Epilepsy", "epilepsy generalized symptomatic", "Symptomatic generalized epilepsy", "Epilepsy, Symptomatic Generalized", "Generalized Epilepsy, Symptomatic", "Symptomatic generalized epilepsy, NOS", "Symptomatic generalized epilepsy (disorder)", "Symptomatic generalized epilepsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary generalized epilepsy", "shortest_name_length": 30}
{"curie": "MONDO:0016746", "names": ["Meninges Melanocytoma", "meninges melanocytoma", "Meningeal Melanocytoma", "meningeal melanocytoma", "Meningeal melanocytoma", "Melanocytoma of Meninges", "melanocytoma of meninges", "Melanocytoma of meninges", "Leptomeningeal Melanocytoma", "Leptomeningeal melanocytoma", "leptomeningeal melanocytoma", "melanocytoma of the meninges", "Melanocytoma of the Meninges", "Melanocytoma of meninges (disorder)", "Melanocytoma of meninges (diagnosis)", "meningeal neoplasm primary melanocytoma", "Meningeal melanocytoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "meningeal melanocytoma", "shortest_name_length": 21}
{"curie": "UMLS:C0347010", "names": ["Metastasis to ureter", "Metastasis to the Ureter", "Metastatic tumor to ureter", "Metastatic tumour to ureter", "Metastatic Tumor to the Ureter", "Metastatic Neoplasm to the Ureter", "ureter neoplasm malignant secondary", "Secondary malignant neoplasm of ureter", "Metastatic malignant neoplasm of ureter", "Metastatic malignant neoplasm to ureter", "Metastatic Malignant Neoplasm in the Ureter", "Metastatic Malignant Neoplasm to the Ureter", "Metastatic malignant neoplasm to ureter (disorder)", "Secondary malignant neoplasm of ureter (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to ureter", "shortest_name_length": 20}
{"curie": "UMLS:C5419870", "names": ["Unresectable Digestive System Mixed Adenoneuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Digestive System Mixed Adenoneuroendocrine Carcinoma", "shortest_name_length": 65}
{"curie": "UMLS:C1336224", "names": ["Stage IIIB Large Cell Lung Cancer", "Stage IIIB Large Cell Lung Carcinoma", "Stage IIIB Large Cell Carcinoma of Lung", "Stage IIIB Large Cell Carcinoma of the Lung", "Stage IIIB Lung Large Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Lung Large Cell Carcinoma AJCC v7", "shortest_name_length": 33}
{"curie": "MONDO:0600001", "names": ["glutaminase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glutaminase deficiency", "shortest_name_length": 22}
{"curie": "UMLS:C0862779", "names": ["Stage IIIA Adenosquamous Lung Cancer", "Stage IIIA Adenosquamous Lung Carcinoma", "Adenosquamous cell lung cancer stage IIIA", "Stage IIIA Adenosquamous Cell Lung Carcinoma", "Stage IIIA Adenosquamous Cell Carcinoma of Lung", "Stage IIIA Lung Adenosquamous Carcinoma AJCC v7", "Stage IIIA Adenosquamous Cell Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenosquamous cell lung cancer stage IIIA", "shortest_name_length": 36}
{"curie": "MONDO:0001009", "names": ["BREAST CYST SOLITARY", "Solitary Breast Cyst", "solitary cyst of breast", "Solitary Cyst of Breast", "Solitary cyst of breast", "solitary cyst of the breast", "Solitary Cyst of the Breast", "Solitary Cyst of the breast", "Solitary cyst of breast (disorder)", "Solitary cyst of unspecified breast", "solitary cyst of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "solitary cyst of breast", "shortest_name_length": 20}
{"curie": "UMLS:C3900096", "names": ["Pineal Gland Astrocytoma", "Adult Pineal Gland Astrocytoma", "adult pineal gland astrocytoma", "pineal gland astrocytoma, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Pineal Gland Astrocytoma", "shortest_name_length": 24}
{"curie": "UMLS:C0015927", "names": ["IUD", "STILLBORN", "Stillborn", "stillborn", "STILLBIRTH", "Stillbirth", "stillborns", "stillbirth", "FETAL DEATH", "stillbirths", "death fetal", "Fetal Death", "fetal death", "Still birth", "Death fetal", "still birth", "Stillbirths", "death fetus", "DEATH FETAL", "Fetal death", "fetus death", "Fetal Deaths", "fetal deaths", "foetal death", "Death foetal", "Fetal demise", "fetus; death", "death; fetal", "DEATH FOETAL", "Death, Fetal", "Fetal Demise", "Foetal death", "births still", "Demise, Fetal", "Deaths, Fetal", "Foetal demise", "Stillbirth NOS", "deadborn fetus", "Prenatal death", "Antenatal death", "Stillbirth, NOS", "SB - Stillbirth", "Late fetal death", "Fetal death, NOS", "stillborn infant", "Foetal death, NOS", "Deadborn fetus NOS", "Death intrauterine", "Death before birth", "INTRAUTERINE DEATH", "intrauterine death", "Intrauterine death", "death intrauterine", "DEATH INTRAUTERINE", "death; intrauterine", "Intra-uterine death", "intrauterine; death", "intra uterine death", "Fetal death (event)", "stillbirth (history)", "Antenatal death, NOS", "fetal death in utero", "Fetal death in utero", "Stillbirth (finding)", "Foetal death in utero", "stillbirth (diagnosis)", "fetal death (diagnosis)", "Intrauterine death, NOS", "IUD - Intrauterine death", "the infant was stillborn", "intrauterine fetal death", "Intrauterine fetal death", "death fetal intrauterine", "Intrauterine Fetal Death", "INTRAUTERINE FETAL DEMISE", "intrauterine fetal demise", "demises fetal intrauterine", "FDIU - Fetal death in utero", "Stillborn or neonatal death", "IUFD - Intrauterine fetal death", "stillborn infant (physical finding)", "peripartum history delivery stillbirth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fetal Death", "shortest_name_length": 3}
{"curie": "MONDO:0016777", "names": ["Inhalation botulism", "inhalation botulism", "Inhalational botulism", "inhalational botulism", "Inhalational botulism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inhalational botulism", "shortest_name_length": 19}
{"curie": "MONDO:0002046", "names": ["aca", "etohism", "Alcoholism", "ETOH ABUSE", "alcoholism", "ETOH abuse", "Alcohol abuse", "Alcohol Abuse", "alcohol abuse", "Ethanol Abuse", "ALCOHOL ABUSE", "Ethanol abuse", "ethanol abuse", "abuse, alcohol", "Abuse, Ethanol", "abuse; alcohol", "alcohol abuses", "alcohol; abuse", "Abuse, Alcohol", "abuses alcohol", "drinking problem", "Problem Drinking", "problem drinking", "drinking problems", "alcohol addiction", "alcohol dependence", "RNDx alcohol abuse", "addiction, alcohol", "AA - Alcohol abuse", "dependence, alcohol", "alcohol use disorder", "problem; alcohol use", "alcohol; use, problem", "Alcohol Use Disorders", "alcohol abuse disorder", "Alcohol abuse (disorder)", "dysfunctional alcohol use", "alcohol abuse (diagnosis)", "Alcohol abuse, unspecified", "RNDx alcohol abuse (diagnosis)", "chronic alcoholic intoxication", "intoxication, chronic alcoholic", "alcoholic intoxication, chronic", "Alcohol abuse, unspecified drinking behavior", "Alcohol abuse, unspecified drinking behaviour"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alcohol abuse", "shortest_name_length": 3}
{"curie": "UMLS:C4525745", "names": ["Stage I Colon Neuroendocrine Tumor", "Stage I Colon Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Colon Neuroendocrine Tumor AJCC v8", "shortest_name_length": 34}
{"curie": "MONDO:0800104", "names": ["IMD105", "immunodeficiency 105", "IMMUNODEFICIENCY 105", "SCID, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive", "severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 105", "shortest_name_length": 6}
{"curie": "MONDO:0004894", "names": ["cyclotropia", "Cyclotropia", "Cyclotropia, NOS", "Cyclotropia (disorder)", "cyclotropia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cyclotropia", "shortest_name_length": 11}
{"curie": "UMLS:C0005417", "names": ["Biliary Fistula", "biliary fistula", "Biliary fistula", "Fistula, Biliary", "Biliary Fistulas", "biliary fistulas", "Bile duct fistula", "Fistulas, Biliary", "bile duct; fistula", "fistula; bile duct", "Fistula of bile duct", "biliary duct fistula", "fistula; common duct", "Biliary tract fistula", "Biliary system fistula", "Fistula of bile duct, NOS", "Fistula of bile duct (disorder)", "biliary duct fistula (diagnosis)", "Perforation of biliary tree with fistula formation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Biliary Fistula", "shortest_name_length": 15}
{"curie": "UMLS:C0280368", "names": ["Stage I Oropharyngeal SCC", "Stage I SCC of Oropharynx", "Stage I SCC of the Oropharynx", "Stage I Oropharyngeal Epidermoid Carcinoma", "Stage I Epidermoid Carcinoma of Oropharynx", "oropharynx squamous cell carcinoma, stage I", "Stage I Oropharyngeal Squamous Cell Carcinoma", "Oropharyngeal squamous cell carcinoma stage I", "Stage I Squamous Cell Carcinoma of Oropharynx", "oropharyngeal squamous cell carcinoma, stage I", "Stage I Epidermoid Carcinoma of the Oropharynx", "epidermoid carcinoma of the oropharynx, stage I", "Stage I Oropharyngeal Throat Squamous Cell Cancer", "Stage I Squamous Cell Carcinoma of the Oropharynx", "stage I squamous cell carcinoma of the oropharynx", "squamous cell carcinoma of the oropharynx, stage I", "Stage I Oropharyngeal Squamous Cell Carcinoma AJCC v6", "Stage I Oropharyngeal Squamous Cell Carcinoma AJCC v7", "Stage I Oropharyngeal Squamous Cell Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oropharyngeal squamous cell carcinoma stage I", "shortest_name_length": 25}
{"curie": "UMLS:C0451948", "names": ["head injury multiple", "Multiple Head Injury", "Injury, Multiple Head", "Head Injury, Multiple", "injury; head, multiple", "multiple head injuries", "Multiple Head Injuries", "Head Injuries, Multiple", "Injuries, Multiple Head", "Multiple injuries of head", "HEAD INJURY TRAUMA MULTIPLE", "multiple head injuries (diagnosis)", "Multiple injuries of head (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Head Injuries, Multiple", "shortest_name_length": 20}
{"curie": "MONDO:0014722", "names": ["RFMN", "ROIFMAN syndrome", "Roifman syndrome", "ROIFMAN SYNDROME", "Roifman syndrome (disorder)", "Roifman syndrome (diagnosis)", "spondyloepiphseal dysplasia, retinal dystrophy and antibody deficiency", "Spondyloepiphseal dysplasia, retinal dystrophy, and antibody deficiency", "SPONDYLOEPIPHYSEAL DYSPLASIA, RETINAL DYSTROPHY, AND ANTIBODY DEFICIENCY", "spondyloepiphyseal dysplasia-retinal dystrophy-immunodeficiency syndrome", "Spondyloepiphyseal dysplasia-retinal dystrophy-immunodeficiency syndrome", "spondyloepiphyseal dysplasia, retinal dystrophy, and antibody deficiency", "Spondyloepiphyseal dysplasia, retinal dystrophy, immunodeficiency syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Roifman syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0004571", "names": ["bowel impaction", "BOWEL IMPACTION", "bowel; impaction", "bowels impaction", "impaction; bowel", "Intestinal impaction", "intestinal impaction", "impaction of intestine", "Impaction of intestine", "Impaction of intestine, NOS", "Other impaction of intestine", "Impaction of intestine (disorder)", "impaction of intestine (diagnosis)", "Impaction of intestine, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intestinal impaction", "shortest_name_length": 15}
{"curie": "MONDO:0003595", "names": ["Sclerosing ALT/WDLPS", "Sclerosing liposarcoma", "Sclerosing Liposarcoma", "sclerosing liposarcoma", "Sclerosing liposarcoma (disorder)", "Sclerosing liposarcoma (diagnosis)", "malignant neoplasm liposarcoma sclerosing", "Sclerosing liposarcoma (morphologic abnormality)", "Sclerosing Atypical Lipomatous Tumor/Well Differentiated Liposarcoma", "Sclerosing Atypical Lipomatous Tumor/Well-Differentiated Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sclerosing liposarcoma", "shortest_name_length": 20}
{"curie": "UMLS:C4321477", "names": ["Hb SS", "Hemoglobin SS", "Sickle Cell (SS only)", "Hemoglobin SS Disease", "Sickle Cell-SS Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sickle Cell-SS Disease", "shortest_name_length": 5}
{"curie": "UMLS:C4289988", "names": ["CMO Type 1", "Aldosterone Synthase Deficiency Type 1", "Corticosterone Methyl Oxidase Deficiency Type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aldosterone Synthase Deficiency Type 1", "shortest_name_length": 10}
{"curie": "UMLS:C4527168", "names": ["Stage IIB Cutaneous (Skin) Melanoma", "Clinical Stage IIB Cutaneous Melanoma AJCC v8", "Clinical Stage IIB Melanoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage IIB Cutaneous Melanoma AJCC v8", "shortest_name_length": 35}
{"curie": "MONDO:0014104", "names": ["CAMRQ4", "ATP8A2 dysequilibrium syndrome", "dysequilibrium syndrome caused by mutation in ATP8A2", "cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4", "CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 4", "cerebellar ataxia, mental retardation, and dysequilibrium syndrome type 4", "cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 4", "cerebellar ataxia, intellectual disability, and dysequilibrium syndrome type 4", "cerebellar ataxia and mental retardation with or without quadrupedal locomotion 4", "CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDAL LOCOMOTION 4", "CEREBELLAR ATAXIA, IMPAIRED INTELLECTUAL DEVELOPMENT, AND DYSEQUILIBRIUM SYNDROME 4", "CEREBELLAR ATAXIA, INTELLECTUAL DEVELOPMENTAL DISORDER, AND DYSEQUILIBRIUM SYNDROME 4", "cerebellar ataxia and intellectual disability with or without quadrupedal locomotion 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 4", "shortest_name_length": 6}
{"curie": "UMLS:C5418810", "names": ["Metastatic Endometrial Endometrioid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Endometrial Endometrioid Adenocarcinoma", "shortest_name_length": 50}
{"curie": "MONDO:0003046", "names": ["Anal Tumor", "anus tumor", "anal tumor", "anal tumors", "Anal Tumors", "Anal neoplasm", "Anus Neoplasm", "tumor of anus", "Tumor of Anus", "anal neoplasm", "Anal Neoplasm", "Tumor of anus", "anus neoplasm", "Tumour of anus", "Neoplasm, Anal", "anus neoplasms", "Neoplasm, Anus", "Anus Neoplasms", "Anal Neoplasms", "Neoplasms, Anal", "Neoplasms, Anus", "neoplasm of anus", "Neoplasm of anus", "Neoplasm of Anus", "tumor of the anus", "Tumor of the Anus", "Anal neoplasm NOS", "Neoplasm of the Anus", "neoplasm of the anus", "anus benign neoplasm", "anus neoplasm (disease)", "Neoplasm of anus (disorder)", "neoplasm of anus (diagnosis)", "Anal Neoplasms, Benign and Malignant", "anal neoplasms, benign and malignant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anus neoplasm", "shortest_name_length": 10}
{"curie": "MONDO:0010877", "names": ["HMSN5", "HMSN 5", "HMSN V", "HMSN Type V", "Type V, HMSN", "CMT with Pyramidal Features", "CMT WITH PYRAMIDAL FEATURES", "CMT with pyramidal features", "Charcot-Marie-Tooth disease type 5", "autosomal dominant spastic paraplegia", "hereditary motor and sensory neuropathy 5", "Hereditary Motor and Sensory Neuropathy 5", "HEREDITARY MOTOR AND SENSORY NEUROPATHY V", "Hereditary Motor And Sensory Neuropathy V", "hereditary motor and sensory neuropathy V", "Hereditary sensory-motor neuropathy type V", "Hereditary sensory-motor neuropathy, type 5", "Hereditary sensory-motor neuropathy, type V", "hereditary motor and sensory neuropathy type 5", "Type V Hereditary Motor and Sensory Neuropathy", "Hereditary motor and sensory neuropathy type V", "Hereditary motor and sensory neuropathy type 5", "familial spastic paraplegia autosomal dominant", "Autosomal Dominant Hereditary Spastic Paraplegia", "Autosomal Dominant Spastic Paraplegia Hereditary", "Autosomal dominant hereditary spastic paraplegia", "Hereditary Autosomal Dominant Spastic Paraplegia", "autosomal dominant spastic paraplegia (diagnosis)", "Hereditary, Spastic Paraplegia, Autosomal Dominant", "Spastic Paraplegia, Autosomal Dominant, Hereditary", "Spastic Paraplegia, Hereditary, Autosomal Dominant", "HMSN V (Hereditary Motor and Sensory Neuropathy Type V)", "Charcot-Marie-Tooth disease-pyramidal features syndrome", "Hereditary motor-sensory neuropathy with pyramidal signs", "Hereditary Motor Sensory Neuropathy with Pyramidal Signs", "Hereditary Motor-Sensory Neuropathy with Pyramidal Signs", "Charcot-Marie-Tooth disease, pyramidal features syndrome", "Hereditary motor and sensory neuropathy type 5 (disorder)", "hereditary motor and sensory neuropathy type 5 (diagnosis)", "Autosomal dominant hereditary spastic paraplegia (disorder)", "hereditary motor and sensory neuropathy with pyramidal features", "PERONEAL MUSCULAR ATROPHY WITH PYRAMIDAL FEATURES, AUTOSOMAL DOMINANT", "Peroneal Muscular Atrophy with Pyramidal Features, Autosomal Dominant", "Spastic paraplegia with hypertrophic sensory-motor neuropathy, type V", "peroneal muscular atrophy with pyramidal features, autosomal dominant", "Spastic paraplegia with hypertrophic motor-sensory neuropathy, type 5", "Charcot-Marie-Tooth Disease with Pyramidal Features, Autosomal Dominant", "CHARCOT-MARIE-TOOTH DISEASE WITH PYRAMIDAL FEATURES, AUTOSOMAL DOMINANT", "Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant", "Charcot Marie Tooth Disease with Pyramidal Features, Autosomal Dominant", "Charcot-Marie-Tooth neuropathy with pyramidal features, autosomal dominant", "CHARCOT-MARIE-TOOTH NEUROPATHY WITH PYRAMIDAL FEATURES, AUTOSOMAL DOMINANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 5", "shortest_name_length": 5}
{"curie": "UMLS:C5446863", "names": ["Locally Advanced Malignant Mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Malignant Mesothelioma", "shortest_name_length": 39}
{"curie": "UMLS:C0677718", "names": ["Stage III Aggressive Non-Hodgkin Lymphoma", "Stage III Aggressive Adult Non-Hodgkin Lymphoma", "stage III aggressive adult non-Hodgkin lymphoma", "aggressive, stage III adult non-Hodgkin lymphoma", "Aggressive Adult Non-Hodgkin's Lymphoma Stage III", "Aggressive Stage III Adult Non-Hodgkin's Lymphoma", "stage III aggressive adult non-Hodgkin's lymphoma", "Stage III Aggressive Adult Non-Hodgkin's Lymphoma", "aggressive adult non-Hodgkin's lymphoma stage III", "aggressive stage III adult non-Hodgkin's lymphoma", "Ann Arbor Stage III Aggressive Adult Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage III Aggressive Adult Non-Hodgkin Lymphoma", "shortest_name_length": 41}
{"curie": "MONDO:0030822", "names": ["RHDA4", "renal hypodysplasia/aplasia 4", "RENAL HYPODYSPLASIA/APLASIA 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal hypodysplasia/aplasia 4", "shortest_name_length": 5}
{"curie": "UMLS:C0273545", "names": ["Superficial injury of eye", "eyeball; injury, superficial", "injury; eyeball, superficial", "injury; superficial, eyeball", "Superficial injury of eye NOS", "Superficial injury of eye, NOS", "Superficial injury of eyeball NOS", "Superficial injury of eye (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Superficial injury of eye", "shortest_name_length": 25}
{"curie": "UMLS:C0339274", "names": ["Corneal epithelial degeneration", "Corneal epithelial degeneration (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Corneal epithelial degeneration", "shortest_name_length": 31}
{"curie": "UMLS:C1511566", "names": ["CBCL", "PCBCL", "B Cell Non-Hodgkin's Lymphoma of Skin", "cutaneous B-cell non-Hodgkin lymphoma", "Cutaneous B-Cell Non-Hodgkin's Lymphoma", "B Cell Non-Hodgkin's Lymphoma of the Skin", "Primary B-Cell Non-Hodgkin Lymphoma of Skin", "Cutaneous (Skin) B-Cell Non-Hodgkin Lymphoma", "Primary Cutaneous B-Cell Non-Hodgkin Lymphoma", "Primary Cutaneous B-Cell Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Cutaneous B-Cell Non-Hodgkin Lymphoma", "shortest_name_length": 4}
{"curie": "UMLS:C0334405", "names": ["Benign androblastoma", "Androblastoma, benign", "Benign arrhenoblastoma", "Arrhenoblastoma, benign", "Sertoli-Leydig cell tumor, well differentiated", "Androblastoma, benign (morphologic abnormality)", "Well Differentiated Ovarian Sertoli-Leydig Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Well Differentiated Ovarian Sertoli-Leydig Cell Tumor", "shortest_name_length": 20}
{"curie": "MONDO:0005216", "names": ["cancer of hypopharynx", "Hypopharyngeal Cancer", "Cancer of Hypopharynx", "hypopharynx carcinoma", "hypopharyngeal cancer", "hypopharyngeal carcinoma", "Carcinoma of Hypopharynx", "carcinoma of hypopharynx", "Hypopharyngeal Carcinoma", "Cancer of the Hypopharynx", "cancer of the hypopharynx", "carcinoma of the hypopharynx", "hypopharyngeal throat cancer", "Hypopharyngeal Throat Cancer", "Carcinoma of the Hypopharynx", "carcinoma of hypopharynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypopharyngeal carcinoma", "shortest_name_length": 21}
{"curie": "MONDO:0054794", "names": ["HYC3", "HYDROCEPHALUS, CONGENITAL, 3, WITH BRAIN ANOMALIES", "hydrocephalus, CONGENITAL, 3, with brain anomalies", "hydrocephalus, congenital, 3, with brain anomalies", "hydrocephalus, nonsyndromic, autosomal recessive 3", "HYDROCEPHALUS, NONSYNDROMIC, AUTOSOMAL RECESSIVE 3, FORMERLY", "hydrocephalus, nonsyndromic, autosomal recessive 3, formerly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hydrocephalus, congenital, 3, with brain anomalies", "shortest_name_length": 4}
{"curie": "UMLS:C0743505", "names": ["ENDOCERVICAL MASS", "Endocervical Mass"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endocervical Mass", "shortest_name_length": 17}
{"curie": "MONDO:0011454", "names": ["patent arterial duct-bicuspid aortic valve-hand anomalies syndrome", "patent ductus arteriosus and bicuspid aortic valve with hand anomalies", "PATENT DUCTUS ARTERIOSUS AND BICUSPID AORTIC VALVE WITH HAND ANOMALIES", "Patent Ductus Arteriosus and Bicuspid Aortic Valve with Hand Anomalies", "patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome", "shortest_name_length": 66}
{"curie": "MONDO:0002636", "names": ["accessory nerve lesion", "disorder of 11th nerve", "Accessory nerve lesion", "Disorder of 11th Nerve", "eleventh nerve disorder", "Eleventh nerve disorder", "Disorders of 11th nerve", "Accessory Nerve Disease", "accessory nerve disease", "n.accessorius; disorder", "Eleventh Nerve Disorder", "Accessory nerve disorder", "Accessory Nerve Disorder", "accessory nerve disorder", "Accessory Nerve Diseases", "disorder accessory nerve", "accessory nerve diseases", "Accessory nerve disorders", "Cranial Nerve XI Diseases", "Disorder of the 11th Nerve", "disorder of the 11th nerve", "accessory XI nerve disease", "disorder of accessory nerve", "Disorder of accessory nerve", "Disorders of accessory nerve", "Disorder of cranial nerve 11", "Accessory nerve disorder NOS", "disease of accessory XI nerve", "Cranial Nerve Eleven Diseases", "disorder of accessory XI nerve", "Eleventh Cranial Nerve Disease", "Cranial Nerve Eleven Disorders", "Spinal Accessory Nerve Diseases", "Eleventh cranial nerve disorder", "Spinal accessory nerve disorder", "Disorder of accessory nerve, NOS", "disorder of accessory [11th] nerve", "Disorders of accessory [11th] nerve", "Disorders of the XIth cranial nerve", "Disorder of accessory nerve (disorder)", "accessory XI nerve disease or disorder", "Disorder of the eleventh cranial nerve", "Disorder of accessory nerve (diagnosis)", "disease (or disorder); nerve, accessory", "Disorders of the eleventh cranial nerve", "disease or disorder of accessory XI nerve", "Eleventh cranial nerve disease or syndrome", "Spinal accessory nerve disease or syndrome", "Disorder of the eleventh cranial nerve, NOS", "cranial nerve; disorder eleventh (accessory)", "disease (or disorder); cranial nerve, eleventh (accessory)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "accessory nerve disorder", "shortest_name_length": 22}
{"curie": "UMLS:C0235834", "names": ["upper motor neuron lesion", "UPPER MOTOR NEURON LESION", "UPPER MOTOR NEURONE LESION", "upper motor neurone lesion", "Upper motor neurone lesion", "lesions motor neuron upper", "lesions motor neurone upper", "Upper motor neurone lesion NOS", "UMNL - Upper motor neurone lesion", "Upper motor neurone lesion (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Upper motor neurone lesion", "shortest_name_length": 25}
{"curie": "MONDO:0015808", "names": ["Follicular Mycosis Fungoides", "Follicular mycosis fungoides", "follicular mycosis fungoides", "folliculotropic mycosis fungoides", "Folliculotropic mycosis fungoides", "Folliculotropic Mycosis Fungoides", "alopecia mucinosa (t cell lymphoma)", "Alopecia mucinosa (T cell lymphoma)", "follicular mucinosis type mycosis fungoides", "Follicular mucinosis type mycosis fungoides", "mycosis fungoides-associated follicular mucinosis", "Mycosis fungoides-associated follicular mucinosis", "Mycosis Fungoides-Associated Follicular Mucinosis", "Follicular mucinosis type mycosis fungoides (disorder)", "Follicular mycosis fungoides (morphologic abnormality)", "follicular mucinosis type mycosis fungoides (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "folliculotropic mycosis fungoides", "shortest_name_length": 28}
{"curie": "MONDO:0008356", "names": ["Posterior radial head dislocation", "posterior dislocation of radial head", "radial heads, posterior dislocation of", "Radial Heads, Posterior Dislocation Of", "RADIAL HEADS, POSTERIOR DISLOCATION OF", "dislocation of the elbow radial head posterior", "posterior dislocation of radial head (diagnosis)", "Congenital Posterior Dislocation of the Radial Head"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radial heads, posterior dislocation of", "shortest_name_length": 33}
{"curie": "UMLS:C4521646", "names": ["0", "Stage 0 Esophageal Adenocarcinoma", "Pathologic Stage 0 Esophageal Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage 0 Esophageal Adenocarcinoma AJCC v8", "shortest_name_length": 1}
{"curie": "MONDO:0001030", "names": ["stable keratoconus", "Keratoconus, stable", "Stable condition keratoconus", "stable condition keratoconus", "keratoconus, stable condition", "Keratoconus, stable condition", "stable keratoconus (diagnosis)", "Keratoconus, stable condition (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratoconus, stable condition", "shortest_name_length": 18}
{"curie": "UMLS:C4683420", "names": ["Stage II Differentiated Thyroid Gland Cancer 55 Years and Older", "Stage II Differentiated Thyroid Gland Carcinoma 55 Years and Older AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Differentiated Thyroid Gland Carcinoma 55 Years and Older AJCC v8", "shortest_name_length": 63}
{"curie": "UMLS:C4552675", "names": ["I", "Stage I Prostate Cancer", "Stage I Prostate Cancer AJCC v8", "Stage I Prostate Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Prostate Cancer AJCC v8", "shortest_name_length": 1}
{"curie": "UMLS:C5420169", "names": ["Nasopharyngeal Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasopharyngeal Lymphoma", "shortest_name_length": 23}
{"curie": "MONDO:0010224", "names": ["Proud syndrome", "Proud Syndrome", "PROUD SYNDROME", "ACC With Abnormal Genitalia", "ACC WITH ABNORMAL GENITALIA", "ACC with abnormal genitalia", "Proud Levine Carpenter syndrome", "Proud-Levine-Carpenter syndrome", "ACC-abnormal genitalia syndrome", "corpus callosum agenesis with abnormal genitalia", "Corpus callosum agenesis-abnormal genitalia syndrome", "corpus callosum agenesis-abnormal genitalia syndrome", "corpus callosum, agenesis of, with abnormal genitalia", "Corpus Callosum, Agenesis of, with Abnormal Genitalia", "CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA", "Corpus callosum agenesis, abnormal genitalia syndrome", "Agenesis of corpus callosum and abnormal genitalia syndrome", "agenesis of corpus callosum and abnormal genitalia syndrome", "Microcephaly-corpus callosum agenesis-abnormal genitalia syndrome", "microcephaly-corpus callosum agenesis-abnormal genitalia syndrome", "seizures-acquired microcephaly-agenesis of corpus callosum syndrome", "Microcephaly, corpus callosum agenesis, abnormal genitalia syndrome", "Agenesis of corpus callosum and abnormal genitalia syndrome (disorder)", "agenesis of corpus callosum and abnormal genitalia syndrome (diagnosis)", "New X-linked syndrome with seizures, acquired micrencephaly, and agenesis of the corpus callosum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corpus callosum agenesis-abnormal genitalia syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0013477", "names": ["CMH20", "hypertrophic cardiomyopathy 20", "NEXN hypertrophic cardiomyopathy", "cardiomyopathy, hypertrophic, 20", "hypertrophic cardiomyopathy type 20", "cardiomyopathy familial hypertrophic 20", "cardiomyopathy, familial hypertrophic, 20", "CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 20", "cardiomyopathy, familial hypertrophic, type 20", "hypertrophic cardiomyopathy caused by mutation in NEXN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophic cardiomyopathy 20", "shortest_name_length": 5}
{"curie": "UMLS:C1266106", "names": ["Sertoli-Leydig cell tumor, retiform", "Sertoli-Leydig cell tumour, retiform", "Ovarian Sertoli-Leydig Cell Tumor with Retiform Elements", "Sertoli-Leydig cell tumor, retiform (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sertoli-Leydig cell tumor, retiform", "shortest_name_length": 35}
{"curie": "UMLS:C5420198", "names": ["Oropharyngeal HPV Negative Squamous Cell Carcinoma", "Oropharyngeal HPV-Negative Squamous Cell Carcinoma", "Oropharyngeal Human Papillomavirus-Negative Squamous Cell Carcinoma", "Oropharyngeal Human Papillomavirus Negative Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oropharyngeal Human Papillomavirus-Negative Squamous Cell Carcinoma", "shortest_name_length": 50}
{"curie": "MONDO:0006630", "names": ["OA spine", "O/A spine", "spondylarthrosis", "Spondarthropathy", "Spondylarthrosis", "Spondyloarthrosis", "spondyloarthrosis", "Bechterew Syndrome", "Spondylarthropathy", "spondylarthropathy", "spondyloarthropathy", "Syndrome, Bechterew", "Spondyloarthropathy", "Spondylarthrosis NOS", "Spondylarthropathies", "Spine Osteoarthritis", "Osteoarthritis;spine", "spinal joint disease", "spondylarthropathies", "Osteoarthritis, Spine", "spondyloarthropathies", "osteoarthritis, spine", "Osteoarthritis spinal", "OSTEOARTHRITIS SPINAL", "Spinal Osteoarthritis", "osteoarthrosis; spine", "spine; osteoarthrosis", "Spondylarthrosis, NOS", "Spinal osteoarthritis", "spinal osteoarthritis", "osteoarthritis spinal", "Spondyloarthropathies", "Osteoarthritis, Spinal", "Osteoarthritis of spine", "Osteoarthritis of Spine", "Spinal osteoarthritis NOS", "Disorder of joint of spine", "Degenerative spine disease", "osteoarthritis of the spine", "Marie-Strumpell Spondylitis", "Marie Strumpell Spondylitis", "Osteoarthritis of the Spine", "Spondylitis, Marie-Strumpell", "OA - Osteoarthritis of spine", "Spondylosis without myelopathy", "spondylosis without myelopathy", "spondyloarthropathy (diagnosis)", "OA - Osteoarthritis of the spine", "spinal joint disease (diagnosis)", "Disorder of joint of spine (disorder)", "Spondylosis without mention of myelopathy", "Spondylosis without myelopathy (disorder)", "spondylosis without myelopathy (diagnosis)", "Spondylosis of unspecified site without mention of myelopathy", "Spondylosis of unspecified site, without mention of myelopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteoarthritis, spine", "shortest_name_length": 8}
{"curie": "MONDO:0044319", "names": ["IDDFSDA", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES", "intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies", "shortest_name_length": 7}
{"curie": "MONDO:0007988", "names": ["autosomal dominant microcephaly", "Microcephaly autosomal dominant", "microcephaly autosomal dominant", "microcephaly, autosomal dominant", "Microcephaly, Autosomal Dominant", "MICROCEPHALY, AUTOSOMAL DOMINANT", "autosomal dominant primary microcephaly", "Autosomal dominant primary microcephaly", "microcephaly (disease), autosomal dominant", "Microcephaly with autosomal dominant inheritance", "microcephaly with autosomal dominant inheritance", "Autosomal dominant primary microcephaly (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant primary microcephaly", "shortest_name_length": 31}
{"curie": "MONDO:0000539", "names": ["striated muscle rhabdoid tumor", "striated muscle tissue rhabdoid tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "striated muscle rhabdoid tumor", "shortest_name_length": 30}
{"curie": "UMLS:C0424024", "names": ["Delusional perception", "Delusional perception (finding)", "Delusion associated with abnormal perception"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Delusional perception", "shortest_name_length": 21}
{"curie": "MONDO:0004419", "names": ["lymphoma-like variant infiltrating bladder urothelial carcinoma", "Infiltrating Bladder Urothelial Carcinoma, Lymphoma-Like Variant", "infiltrating bladder urothelial carcinoma, lymphoma-like variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphoma-like variant infiltrating bladder urothelial carcinoma", "shortest_name_length": 63}
{"curie": "UMLS:C0861611", "names": ["Stage III Mouth Epidermoid Carcinoma", "Stage III Mouth Squamous Cell Carcinoma", "Stage III Epidermoid Carcinoma of Mouth", "Stage III Squamous Cell Carcinoma of Mouth", "Stage III Oral Cavity Squamous Cell Cancer", "Stage III Oral Cavity Epidermoid Carcinoma", "Stage III Epidermoid Carcinoma of the Mouth", "Stage III Epidermoid Carcinoma of Oral Cavity", "Stage III Oral Cavity Squamous Cell Carcinoma", "Stage III Squamous Cell Carcinoma of the Mouth", "Stage III Squamous Cell Carcinoma of Oral Cavity", "Stage III Epidermoid Carcinoma of the Oral Cavity", "Squamous cell carcinoma of the oral cavity stage III", "Stage III Squamous Cell Carcinoma of the Oral Cavity", "Stage III Oral Cavity Squamous Cell Carcinoma AJCC v7", "Stage III Oral Cavity Squamous Cell Carcinoma AJCC v6", "Stage III Oral Cavity Squamous Cell Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Squamous cell carcinoma of the oral cavity stage III", "shortest_name_length": 36}
{"curie": "UMLS:C0160342", "names": ["injury of esophagus with open wound into cavity", "Injury to esophagus with open wound into cavity", "Injury to Esophagus with Open Wound into Cavity", "injury of esophagus with open wound into cavity (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "injury of esophagus with open wound into cavity", "shortest_name_length": 47}
{"curie": "MONDO:0021953", "names": ["Tuberculous fibrosis of lung", "Tuberculous Fibrosis of Lung", "tuberculous fibrosis of lung", "fibrotic pulmonary tuberculosis", "Tuberculous fibrosis of lung (disorder)", "Tuberculous fibrosis of lung, unspecified", "fibrotic pulmonary tuberculosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tuberculous fibrosis of lung", "shortest_name_length": 28}
{"curie": "UMLS:C0272392", "names": ["tonsil ulcer", "tonsils ulcer", "tonsil; ulcer", "tonsil ulcers", "Ulcer, tonsil", "ulcer; tonsil", "tonsils ulcers", "ulcer of tonsil", "Tonsillar ulcer", "Ulcer of tonsil", "tonsillar ulcer", "Tonsil(s) Ulcer(s)", "Ulcer of tonsil (disorder)", "tonsillar ulcer (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ulcer of tonsil", "shortest_name_length": 12}
{"curie": "MONDO:0020814", "names": ["Miliaria alba", "miliaria alba", "miliaria; alba", "alba; miliaria", "Miliaria alba (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "miliaria alba", "shortest_name_length": 13}
{"curie": "MONDO:0021237", "names": ["adrenal medulla tumor", "Adrenal Medulla Tumor", "adrenal medulla cancer", "tumor of adrenal medulla", "Tumor of adrenal medulla", "Adrenal Medulla Neoplasm", "adrenal medulla neoplasm", "Tumour of adrenal medulla", "Medullar adrenal neoplasia", "neoplasm of adrenal medulla", "Neoplasm of adrenal medulla", "Neoplasm of the adrenal medulla", "adrenal medulla neoplasm (disease)", "Neoplasm of adrenal medulla (disorder)", "neoplasm of adrenal medulla (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adrenal medulla neoplasm", "shortest_name_length": 21}
{"curie": "UMLS:C1335667", "names": ["Reactive Lymphocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reactive Lymphocytosis", "shortest_name_length": 22}
{"curie": "MONDO:0016721", "names": ["pineal tumor of neuroepithelial tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pineal tumor of neuroepithelial tissue", "shortest_name_length": 38}
{"curie": "UMLS:C3272824", "names": ["Colorectal Hodgkin Lymphoma", "Primary Colorectal Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Hodgkin Lymphoma", "shortest_name_length": 27}
{"curie": "MONDO:0001053", "names": ["acute infection of pinna", "Acute infection of pinna", "Acute infection of pinna (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute infection of pinna", "shortest_name_length": 24}
{"curie": "UMLS:C3897751", "names": ["Recurrent Gliomatosis Cerebri", "Recurrent Childhood Gliomatosis Cerebri", "recurrent childhood gliomatosis cerebri"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Gliomatosis Cerebri", "shortest_name_length": 29}
{"curie": "MONDO:0014815", "names": ["MRT52", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 52", "mental retardation, autosomal recessive 52", "mental retardation, autosomal recessive type 52", "intellectual disability, autosomal recessive 52", "intellectual disability, autosomal recessive type 52", "autosomal recessive intellectual developmental disorder 52", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 52", "intellectual developmental disorder, autosomal recessive 52", "LMAN2L autosomal recessive non-syndromic intellectual disability", "autosomal recessive non-syndromic intellectual disability caused by mutation in LMAN2L"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 52", "shortest_name_length": 5}
{"curie": "MONDO:0021501", "names": ["Benign Small Intestine Tumor", "benign small intestine tumor", "benign small intestinal tumor", "Benign Small Intestinal Tumor", "benign small intestine neoplasm", "Benign tumor of small intestine", "Benign Small Intestine Neoplasm", "small intestine benign neoplasm", "Benign Tumor of Small Intestine", "benign tumor of small intestine", "Benign small intestinal neoplasm", "Benign tumour of small intestine", "benign small intestinal neoplasm", "Benign Small Intestinal Neoplasm", "Benign Neoplasm of Small Intestine", "benign neoplasm of small intestine", "Benign neoplasm of small intestine", "benign tumor of the small intestine", "Benign Tumor of the Small Intestine", "Benign Small Intestinal Neoplasm NOS", "Benign small intestinal neoplasm NOS", "benign neoplasm of the small intestine", "Benign Neoplasm of the Small Intestine", "Benign neoplasm of small intestine NOS", "Benign neoplasm of small intestine, NOS", "Benign neoplasm of small intestine (disorder)", "Benign neoplasm of duodenum, jejunum and ileum", "benign neoplasm of small intestine (diagnosis)", "Benign neoplasm of duodenum, jejunum, and ileum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of small intestine", "shortest_name_length": 28}
{"curie": "UMLS:C0919662", "names": ["prolong menstruation", "menstruation prolonged", "prolonged menstruation", "Menstrual cycle prolonged", "prolonged menstrual cycle"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Menstrual cycle prolonged", "shortest_name_length": 20}
{"curie": "UMLS:C0334002", "names": ["Stromal Hyperplasia", "Stromal hyperplasia", "stromal hyperplasia", "Hyperplasia, stromal", "Stromal hyperplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stromal hyperplasia", "shortest_name_length": 19}
{"curie": "MONDO:0017910", "names": ["DHS", "Xerocytosis", "xerocytosis", "Dessicocytosis", "Xerocytosis (disorder)", "hereditary xerocytosis", "xerocytosis hereditary", "Hereditary xerocytosis", "Hereditary Xerocytosis", "hereditary desiccytosis", "Desiccytosis hereditary", "Xerocytosis, hereditary", "XEROCYTOSIS, HEREDITARY", "Desiccytosis, hereditary", "DESICCYTOSIS, HEREDITARY", "Dehydrated hereditary stomatocytosis", "dehydrated hereditary stomatocytosis", "DEHYDRATED HEREDITARY STOMATOCYTOSIS", "Dehydrated hereditary stomatocytosis (disorder)", "Dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and-or perinatal edema hemophagocytic lymphohistiocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dehydrated hereditary stomatocytosis", "shortest_name_length": 3}
{"curie": "UMLS:C0279740", "names": ["Grade I Salivary Gland Mucoepidermoid Carcinoma", "low-grade salivary gland mucoepidermoid carcinoma", "salivary gland mucoepidermoid carcinoma low grade", "Low Grade Salivary Gland Mucoepidermoid Carcinoma", "mucoepidermoid carcinoma low grade, salivary gland", "low grade mucoepidermoid carcinoma, salivary gland", "Grade I Mucoepidermoid Carcinoma of Salivary Gland", "Low-Grade Mucoepidermoid Carcinoma of Salivary Gland", "Grade I Mucoepidermoid Carcinoma of the Salivary Gland", "Low-Grade Mucoepidermoid Carcinoma of the Salivary Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Grade Salivary Gland Mucoepidermoid Carcinoma", "shortest_name_length": 47}
{"curie": "MONDO:0024877", "names": ["clitoris tumor", "clitoris neoplasm", "tumor of clitoris", "clitoral neoplasm", "Neoplasm of clitoris", "neoplasm of clitoris", "Neoplasm of clitoris (disorder)", "neoplasm of clitoris (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "clitoris neoplasm", "shortest_name_length": 14}
{"curie": "MONDO:0033810", "names": ["isolated iridoschisis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated iridoschisis", "shortest_name_length": 21}
{"curie": "MONDO:0010744", "names": ["Thrombocytopenia with Elevated Serum Iga and Renal Disease", "thrombocytopenia with elevated serum IgA and renal disease", "THROMBOCYTOPENIA WITH ELEVATED SERUM IgA AND RENAL DISEASE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombocytopenia with elevated serum IgA and renal disease", "shortest_name_length": 58}
{"curie": "MONDO:0009454", "names": ["ICF1", "ICF syndrome 1", "immunodeficiency syndrome, variable", "centromeric instability, immunodeficiency syndrome", "Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1", "IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 1", "immunodeficiency-centromeric instability-facial anomalies syndrome 1", "immunodeficiency-centromeric instability-Facial anomalies syndrome type 1", "DNMT3B immunodeficiency-centromeric instability-facial anomalies syndrome", "immunodeficiency-centromeric instability-facial anomalies syndrome type 1", "immune deficiency, variable, with centromeric instability of chromosomes 1, 9, and 16", "immunodeficiency-centromeric instability-facial anomalies syndrome caused by mutation in DNMT3B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency-centromeric instability-facial anomalies syndrome 1", "shortest_name_length": 4}
{"curie": "UMLS:C1334750", "names": ["Methotrexate-Associated Peripheral T-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Methotrexate-Associated Peripheral T-Cell Lymphoma", "shortest_name_length": 50}
{"curie": "UMLS:C5238361", "names": ["Locally Advanced Primary Peritoneal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Primary Peritoneal Carcinoma", "shortest_name_length": 45}
{"curie": "UMLS:C4317089", "names": ["strawberry nevus", "Strawberry Nevus", "Cellular Hemangioma", "juvenile hemangioma", "cellular hemangioma", "Juvenile Hemangioma", "Juvenile hemangioma", "Infantile hemangioma", "Infantile Hemangioma", "infantile hemangioma", "Infantile haemangioma", "Juvenile Capillary Hemangioma", "juvenile capillary hemangioma", "Infantile Hemangioendothelioma", "infantile hemangioendothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infantile hemangioma", "shortest_name_length": 16}
{"curie": "MONDO:0018338", "names": ["APDS", "IMD14", "PASLI", "IMD14A", "APD Syndrome", "Immunodeficiency 14", "activated PI3K-delta syndrome", "Activated PI3K-delta syndrome", "Activated PI3K-Delta Syndrome", "ACTIVATED PI3K-DELTA SYNDROME", "Activated PI3K-delta Syndrome", "PIK3CD-Associated Immunodeficiency", "APDS (Activated PI3K-delta Syndrome)", "Activated PI3K-delta syndrome (disorder)", "IMMUNODEFICIENCY 14A, AUTOSOMAL DOMINANT", "Immunodeficiency 14A, Autosomal Dominant", "activated phosphoinositide 3-kinase delta syndrome", "activated phosphoinositide 3-kinase delta syndrome (diagnosis)", "p110-delta-activating mutation causing senescent T cells, lymphadenopathy and immunodeficiency", "p110-DELTA-ACTIVATING MUTATION CAUSING SENESCENT T CELLS, LYMPHADENOPATHY, AND IMMUNODEFICIENCY", "Senescent T-cells-lymphadenopathy-immunodeficiency syndrome due to p110delta-activating mutation", "senescent T-cells-lymphadenopathy-immunodeficiency syndrome due to p110delta-activating mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "activated PI3K-delta syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C5239069", "names": ["Advanced Dedifferentiated Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Dedifferentiated Liposarcoma", "shortest_name_length": 37}
{"curie": "MONDO:0006118", "names": ["Fibrosis breast", "Breast Fibrosis", "FIBROSIS BREAST", "Breast fibrosis", "fibrosis breast", "breast fibrosis", "breasts fibrosis", "FIBROSIS, BREAST", "fibrosis; breast", "breast; fibrosis", "Fibrosis of Breast", "fibrosis of breast", "breast fibrosclerosis", "Breast Fibrosclerosis", "Fibrosis of the Breast", "fibrosclerosis; breast", "Fibrosis of the breast", "breast; fibrosclerosis", "fibrosis of the breast", "fibrosclerosis of breast", "Fibrosclerosis of Breast", "Fibrosclerosis of breast", "fibrosclerosis of the breast", "Fibrosclerosis of the Breast", "Fibrosclerosis of breast (disorder)", "fibrosclerosis of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast fibrosis", "shortest_name_length": 15}
{"curie": "UMLS:C0278584", "names": ["metastatic cervix cancer", "Cervix cancer metastatic", "cervix cancer, metastatic", "metastatic cervical cancer", "cervical cancer metastatic", "cervical cancer, metastatic", "metastatic cancer of the cervix", "cancer of the cervix, metastatic", "metastatic uterine cervix cancer", "Secondary Carcinoma to the Cervix", "uterine cervix cancer, metastatic", "Metastatic Carcinoma to the Cervix", "metastatic carcinoma of the cervix", "uterine cervical cancer, metastatic", "carcinoma of the cervix, metastatic", "Secondary Carcinoma to the Cervix Uteri", "Metastatic Carcinoma to the Cervix Uteri", "Secondary Carcinoma to the Uterine Cervix", "Metastatic Carcinoma in the Uterine Cervix", "Metastatic Carcinoma to the Uterine Cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Carcinoma to the Uterine Cervix", "shortest_name_length": 24}
{"curie": "UMLS:C4727358", "names": ["Recurrent Prostate Acinar Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Prostate Acinar Adenocarcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0006951", "names": ["Retinal vein occlusion", "RETINAL VEIN OCCLUSION", "Retinal Vein Occlusion", "Occlusion retinal vein", "retina; occlusion vein", "occlusion retinal vein", "OCCLUSION RETINAL VEIN", "retinal vein occlusion", "retinal vein occlusions", "THROMBOSIS RETINAL VEIN", "Thrombosis;vein;retinal", "vein; retina, occlusion", "Thrombosis retinal vein", "RETINAL VEIN THROMBOSIS", "vein; occlusion, retina", "Retinal Vein Thrombosis", "occlusion; retina, vein", "retinal vein thrombosis", "Retinal Vein Thromboses", "Retinal Vein Occlusions", "Retinal vein thrombosis", "Occlusion, Retinal Vein", "Vein Occlusion, Retinal", "occlusion; vein, retina", "Thrombosis, Retinal Vein", "Vein Thrombosis, Retinal", "occlusion of retinal vein", "Occlusion of retinal vein", "thrombosis of retinal vein", "Occlusion, of retinal vein", "occlusion, of retinal vein", "Thrombosis of retinal vein", "retinal vein thrombosis (diagnosis)", "Occlusion of retinal vein (disorder)", "Thrombosis of retinal vein (disorder)", "occlusion of retinal vein (diagnosis)", "occlusion of retinal vein (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal vein occlusion", "shortest_name_length": 22}
{"curie": "MONDO:0024189", "names": ["neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset", "shortest_name_length": 75}
{"curie": "MONDO:0007728", "names": ["ACNINV1", "Acne inversa, familial", "acne inversa, familial", "ACNE INVERSA, FAMILIAL", "acne inversa, familial, 1", "ACNE INVERSA, FAMILIAL, 1", "NCSTN familial acne inversa", "acne inversa, familial, type 1", "Hidradenitis suppurativa, familial", "hidradenitis suppurativa, familial", "HIDRADENITIS SUPPURATIVA, FAMILIAL", "familial acne inversa caused by mutation in NCSTN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acne inversa, familial, 1", "shortest_name_length": 7}
{"curie": "UMLS:C1332263", "names": ["Anal Extramucosal (Perianal) Adenocarcinoma", "Extramucosal (Perianal) Adenocarcinoma of Anus", "Extramucosal (Perianal) Adenocarcinoma of the Anus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anal Extramucosal (Perianal) Adenocarcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0019653", "names": ["familial idiopathic steroid-resistant nephrotic syndrome with minimal changes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial idiopathic steroid-resistant nephrotic syndrome with minimal changes", "shortest_name_length": 77}
{"curie": "MONDO:0002571", "names": ["PCNSL", "Microglioma", "microglioma", "cns lymphoma", "CNS lymphoma", "CNS LYMPHOMA", "lymphoma cns", "CNS Lymphoma", "cns lymphomas", "[M]Microglioma", "cns lymphoma primary", "Primary CNS Lymphoma", "Primary CNS lymphoma", "primary lymphoma cns", "primary cns lymphoma", "primary CNS lymphoma", "primary lymphoma, CNS", "lymphoma, primary CNS", "CNS lymphoma, primary", "primary brain lymphoma", "Primary brain lymphoma", "Microglioma (disorder)", "primary lymphoma of CNS", "microglioma (diagnosis)", "malignant lymphomas of CNS", "Malignant Lymphomas of CNS", "PCNSL - Primary CNS lymphoma", "Malignant Lymphomas of the CNS", "malignant lymphomas of the CNS", "central nervous system lymphoma", "Central nervous system lymphoma", "central lymphoma nervous system", "Central Nervous System Lymphoma", "lymphoma of central nervous system", "Primary central nervous system lymphoma", "primary central nervous system lymphoma", "Primary Central Nervous System Lymphoma", "lymphoma, primary central nervous system", "central nervous system lymphoma, primary", "malignant lymphoma of central nervous system", "malignant lymphoma of central nervous system (diagnosis)", "malignant neoplasm lymphoma primary central nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary central nervous system lymphoma", "shortest_name_length": 5}
{"curie": "MONDO:0013768", "names": ["GACI2", "ABCC6 arterial calcification of infancy", "ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 2", "arterial calcification, generalized, of infancy, 2", "arterial calcification, generalized, of infancy, type 2", "arterial calcification of infancy caused by mutation in ABCC6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arterial calcification, generalized, of infancy, 2", "shortest_name_length": 5}
{"curie": "UMLS:C0344461", "names": ["Oligodendroblastoma", "Oligodendroblastomas", "Oligodendroblastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oligodendroblastoma", "shortest_name_length": 19}
{"curie": "UMLS:C1960545", "names": ["Cytomegaloviral enteritis", "Cytomegalovirus enteritis", "enteritis viral cytomegaloviral", "Cytomegaloviral enteritis (disorder)", "Cytomegaloviral enteritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cytomegaloviral enteritis", "shortest_name_length": 25}
{"curie": "UMLS:C0948036", "names": ["Gastric ulcer helicobacter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric ulcer helicobacter", "shortest_name_length": 26}
{"curie": "MONDO:0004497", "names": ["Late Syphilis", "late syphilis", "Late syphilis", "syphilis; late", "Syphilis (late)", "late; syphilitic", "syphilis tertiary", "Tertiary syphilis", "tertiary syphilis", "SYPHILIS TERTIARY", "Tertiary Syphilis", "syphilis; tertiary", "Late syphilis, NOS", "Syphilis, tertiary", "tertiary; syphilitic", "late tertiary syphilis", "Late tertiary syphilis", "Late syphilis (disorder)", "late syphilis (diagnosis)", "Late syphilis, unspecified", "Tertiary Treponema pallidum infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tertiary syphilis", "shortest_name_length": 13}
{"curie": "MONDO:0017138", "names": ["G syndrome", "BBB syndrome", "GBBB syndrome", "Opitz syndrome", "Opitz G Syndrome", "Opitz G syndrome", "Opitz GBBB syndrome", "Opitz-GBBB syndrome", "Opitz BBBG syndrome", "Opitz-Frias syndrome", "Opitz G/BBB syndrome", "Opitz G/BBB Syndrome", "Opitz-G syndrome, type 2", "Opitz GBBB syndrome type I", "hypospadias-dysphagia syndrome", "hypospadias-dysphagia, syndrome", "hypertelorism hypospadias syndrome", "hypospadias-hypertelorism syndrome", "telecanthus with associated abnormalities", "Congenital cleft larynx and Opitz-Frias syndrome", "hypertelorism with esophageal abnormality and hypospadias", "hypertelorism-oesophageal abnormality-hypospadias syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Opitz G/BBB syndrome", "shortest_name_length": 10}
{"curie": "UMLS:C1336370", "names": ["Stage IVB Hodgkin Lymphoma", "Stage IVB Hodgkin's Disease", "Hodgkin's Disease Stage IVB", "Stage IVB Hodgkin's Lymphoma", "Hodgkin's Lymphoma Stage IVB", "Ann Arbor Stage IVB Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage IVB Hodgkin Lymphoma", "shortest_name_length": 26}
{"curie": "MONDO:0030718", "names": ["SPGF67", "spermatogenic failure 67", "SPERMATOGENIC FAILURE 67"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 67", "shortest_name_length": 6}
{"curie": "MONDO:0000531", "names": ["bronchus mucoepidermoid carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bronchus mucoepidermoid carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0012547", "names": ["NS4", "NOONAN SYNDROME 4", "Noonan Syndrome 4", "Noonan syndrome 4", "SOS1 Noonan syndrome", "Noonan syndrome type 4", "SOS1 gene related Noonan syndrome", "Noonan syndrome caused by mutation in SOS1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Noonan syndrome 4", "shortest_name_length": 3}
{"curie": "UMLS:C4330179", "names": ["HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma by AJCC v8 cTNM Stage", "HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma by AJCC v8 Clinical Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma by AJCC v8 Clinical Stage", "shortest_name_length": 73}
{"curie": "UMLS:C0001969", "names": ["drunk", "Drunk", "drunks", "inebriety", "DRUNKENNESS", "inebriation", "drunkenness", "Drunkenness", "Drunkennesses", "heavy drinker", "Inebriety NOS", "Drunkenness NOS", "Abuse;alcohol;acute", "Alcohol intoxication", "Alcohol Intoxication", "intoxication alcohol", "alcohol intoxication", "ALCOHOL INTOXICATION", "intoxication; alcohol", "alcohol; intoxication", "Intoxication (Alcohol)", "alcoholic intoxication", "Alcoholic Intoxication", "Intoxication, Alcoholic", "acute alcohol intoxication", "Alcohol intoxication (disorder)", "alcohol intoxication (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alcoholic Intoxication", "shortest_name_length": 5}
{"curie": "UMLS:C0266551", "names": ["iris notch", "Cleft iris", "Notched iris", "IRIS COLOBOMA", "coloboma iris", "iris coloboma", "Iris coloboma", "COLOBOMA IRIDIS", "coloboma iridis", "Coloboma of iris", "coloboma of iris", "Congenital coloboma of iris", "coloboma of iris (diagnosis)", "Congenital coloboma of iris (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital coloboma of iris", "shortest_name_length": 10}
{"curie": "MONDO:0010645", "names": ["OCR", "OCRL", "OCRL1", "Ocrl1", "Lowe disease", "Lowe Disease", "Lowe Syndrome", "lowe syndrome", "disease lowes", "Lowe syndrome", "LOWE SYNDROME", "lowes syndrome", "lowe's syndrome", "Lowe's syndrome", "Lowe syndrome (LS)", "Lowe Bickel Syndrome", "lowe-bickel syndrome", "Lowe-Bickel Syndrome", "Lowe-Bickel syndrome", "Lowe syndrome (disorder)", "oculocerebrorenal syndrome", "Oculocerebrorenal Syndrome", "Cerebrooculorenal Syndrome", "Oculocerebrorenal syndrome", "cerebrooculorenal syndrome", "Oculocerebrorenal dystrophy", "Lowe's syndrome (diagnosis)", "OCULOCEREBRORENAL DYSTROPHY", "Renal-Oculocerebrodystrophy", "Oculocerebrorenal Dystrophy", "Renal-oculocerebrodystrophy", "Renal Oculocerebrodystrophy", "oculocerebrorenal dystrophy", "oculocerebrorenal; dystrophy", "Cerebro-oculorenal dystrophy", "Cerebro-Oculo-Renal Syndrome", "Cerebro Oculo Renal Syndrome", "dystrophy; oculocerebrorenal", "Dystrophy, Oculocerebrorenal", "oculo-cerebro-renal syndrome", "oculo-cerebro-renal dystrophy", "Lowe-Terrey-MacLachlan Syndrome", "Lowe oculocerebrorenal syndrome", "Lowe-Terrey-MacLachlan syndrome", "lowe oculocerebrorenal syndrome", "Lowe Terrey MacLachlan Syndrome", "Lowe Oculocerebrorenal Syndrome", "LOWE OCULOCEREBRORENAL SYNDROME", "Lowe oculocerebrorenal dystrophy", "Lowe syndrome, X-linked recessive", "Lowe oculo-cerebro-renal syndrome", "Lowe oculo-cerebro-renal dystrophy", "oculocerebrorenal syndrome of Lowe", "Oculocerebrorenal Syndrome of Lowe", "Oculocerebrorenal syndrome of Lowe", "oculocerebrorenal (OCR, OCRL) syndrome", "Phosphatidylinositol 4,5-biphosphate 5-phosphatase deficiency", "phosphatidylinositol 4,5-biphosphate 5-phosphatase deficiency", "Phosphatidylinositol 4,5-Bisphosphate 5-Phosphatase Deficiency", "Phosphatidylinositol 4,5 Bisphosphate 5 Phosphatase Deficiency", "Phosphatidylinositol-4,5-bisphosphate-5-phosphatase deficiency", "PHOSPHATIDYLINOSITOL 4,5-BISPHOSPHATE 5-PHOSPHATASE DEFICIENCY", "Phosphatidylinositol-4,5-Bisphosphate-5-Phosphatase Deficiency", "phosphatidylinositol 4,5-bisphosphate 5-phosphatase deficiency", "Deficiency, Phosphatidylinositol-4,5-Bisphosphate-5-Phosphatase"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculocerebrorenal syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0017599", "names": ["SDRPL", "splenic diffuse red pulp lymphoma", "Splenic diffuse red pulp lymphoma", "Splenic diffuse red pulp small B-cell lymphoma", "Splenic Diffuse Red Pulp Small B-Cell Lymphoma", "splenic diffuse red pulp small B-cell lymphoma", "Splenic diffuse red pulp small B-cell lymphoma (disorder)", "Splenic diffuse red pulp small B-cell lymphoma (diagnosis)", "Splenic diffuse red pulp small B-cell lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "splenic diffuse red pulp small B-cell lymphoma", "shortest_name_length": 5}
{"curie": "UMLS:C0399558", "names": ["GOC", "Sialo-odontogenic cyst", "Glandular Odontogenic Cyst", "Glandular odontogenic cyst", "Glandular odontogenic cyst (disorder)", "Glandular odontogenic cyst (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Glandular odontogenic cyst", "shortest_name_length": 3}
{"curie": "MONDO:0014560", "names": ["AI1F", "AMBN amelogenesis imperfecta", "amelogenesis imperfecta type IF", "amelogenesis imperfecta type 1F", "AMELOGENESIS IMPERFECTA, TYPE IF", "amelogenesis imperfecta, type IF", "amelogenesis imperfecta, type 1F", "amelogenesis imperfecta hypoplastic type IF", "amelogenesis imperfecta, hypoplastic type 1F", "AMELOGENESIS IMPERFECTA, HYPOPLASTIC TYPE IF", "amelogenesis imperfecta caused by mutation in AMBN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amelogenesis imperfecta type 1F", "shortest_name_length": 4}
{"curie": "UMLS:C0751713", "names": ["Sporadic inclusion body myositis", "Sporadic Inclusion Body Myositis", "Inclusion Body Myositis, Sporadic", "Inclusion Body Myopathy, Sporadic", "Myositis, Inclusion Body, Sporadic", "Myopathy, Inclusion Body, Sporadic", "Sporadic inclusion body myositis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Inclusion Body Myopathy, Sporadic", "shortest_name_length": 32}
{"curie": "MONDO:0018678", "names": ["polyclonal hyperviscosity syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyclonal hyperviscosity syndrome", "shortest_name_length": 34}
{"curie": "MONDO:0009813", "names": ["NBO", "CMO", "CRMO", "CNO/CRMO", "Non-bacterial Osteomyelitis", "non-bacterial osteomyelitis", "chronic multifocal osteomyelitis", "Chronic multifocal osteomyelitis", "osteomyelitis chronic multifocal", "OSTEOMYELITIS, CHRONIC MULTIFOCAL", "Osteomyelitis, Chronic Multifocal", "Multifocal osteomyelitis, chronic", "osteomyelitis, chronic multifocal", "multifocal osteomyelitis, chronic", "osteomyelitis; chronic, multifocal", "CRMO - Chronic multifocal osteomyelitis", "CHRONIC RECURRENT MULTIFOCAL OSTEOMYELITIS", "Chronic recurrent multifocal osteomyelitis", "chronic recurrent multifocal osteomyelitis", "Chronic Recurrent Multifocal Osteomyelitis", "chronic multifocal osteomyelitis (diagnosis)", "Chronic multifocal osteomyelitis, unspecified site", "Chronic multifocal osteomyelitis, site unspecified", "chronic recurrent multifocal osteomyelitis (disease)", "chronic nonbacterial osteomyelitis/chronic recurrent multifocal osteomyelitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic recurrent multifocal osteomyelitis", "shortest_name_length": 3}
{"curie": "MONDO:0000065", "names": ["microvascular complications of diabetes", "microvascular complications of diabetes, susceptibility"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microvascular complications of diabetes, susceptibility", "shortest_name_length": 39}
{"curie": "UMLS:C5418794", "names": ["Locally Advanced Vulvar Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Vulvar Carcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C2981257", "names": ["Stage IVA Mucosal Melanoma of the Head and Neck", "Stage IVA Mucosal Melanoma of the Head and Neck AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Mucosal Melanoma of the Head and Neck AJCC v7", "shortest_name_length": 47}
{"curie": "MONDO:0012491", "names": ["WM2", "macroglobulinemia, Waldenstrom, 2", "macroglobulinemia, WALDENSTROM, susceptibility to, 2", "MACROGLOBULINEMIA, WALDENSTROM, SUSCEPTIBILITY TO, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macroglobulinemia, Waldenstrom, 2", "shortest_name_length": 3}
{"curie": "MONDO:0012953", "names": ["CRCS10", "POLD1 colorectal cancer", "susceptibility to colorectal cancer 10", "COLORECTAL CANCER, SUSCEPTIBILITY TO, 10", "colorectal cancer, susceptibility to, 10", "colorectal cancer, susceptibility to, type 10", "colorectal cancer caused by mutation in POLD1", "colorectal cancer, susceptibility to, on chromosome 19Q", "COLORECTAL CANCER, SUSCEPTIBILITY TO, ON CHROMOSOME 19q"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorectal cancer, susceptibility to, 10", "shortest_name_length": 6}
{"curie": "UMLS:C4744387", "names": ["Suprasellar Germinoma", "Germinoma of the Suprasellar Region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Suprasellar Germinoma", "shortest_name_length": 21}
{"curie": "MONDO:0012537", "names": ["SHFLD2", "SPLIT-HAND/FOOT MALFORMATION WITH LONG BONE DEFICIENCY 2", "split-hand/foot malformation with long bone deficiency 2", "Split-Hand-Foot Malformation With Long Bone Deficiency 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "split-hand/foot malformation with long bone deficiency 2", "shortest_name_length": 6}
{"curie": "MONDO:0007371", "names": ["Cornea guttata with anterior polar cataract", "cornea guttata with anterior polar cataract", "Cornea Guttata with Anterior Polar Cataracts", "CORNEA GUTTATA WITH ANTERIOR POLAR CATARACTS", "cornea guttata with anterior polar cataracts", "Familial congenital cornea guttata with anterior polar cataracts", "familial congenital cornea guttata with anterior polar cataracts (type)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cornea guttata with anterior polar cataracts", "shortest_name_length": 43}
{"curie": "UMLS:C5420844", "names": ["Simple Hamartoma of the Retinal Pigment Epithelium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Simple Hamartoma of the Retinal Pigment Epithelium", "shortest_name_length": 50}
{"curie": "MONDO:0013196", "names": ["HNPCC8", "LYNCH8", "Lynch syndrome 8", "LYNCH SYNDROME 8", "EPCAM hereditary nonpolyposis colon cancer", "hereditary nonpolyposis colorectal cancer type 8", "COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 8", "Colorectal Cancer, Hereditary Nonpolyposis, Type 8", "colorectal cancer, hereditary nonpolyposis, type 8", "hereditary nonpolyposis colon cancer caused by mutation in EPCAM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lynch syndrome 8", "shortest_name_length": 6}
{"curie": "MONDO:0011801", "names": ["SCAN1", "spinocerebellar ataxia with axonal neuropathy", "spinocerebellar ataxia with axonal neuropathy type 1", "Spinocerebellar ataxia with axonal neuropathy type 1", "spinocerebellar ataxia type 1 with axonal neuropathy", "Spinocerebellar ataxia with axonal neuropathy type 1 (disorder)", "autosomal recessive spinocerebellar ataxia with axonal neuropathy", "spinocerebellar ataxia autosomal recessive with axonal neuropathy", "Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy", "spinocerebellar ataxia, autosomal recessive, with axonal neuropathy", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE, WITH AXONAL NEUROPATHY", "spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE, WITH AXONAL NEUROPATHY 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1", "shortest_name_length": 5}
{"curie": "MONDO:0100441", "names": ["RCD2", "CACD1", "CORD6", "choroidal sclerosis", "cone-rod dystrophy 6", "retinal cone dystrophy 2", "cone-rod dystrophy type 6", "GUCY2D cone-rod dystrophy", "dominant GUCY2D retinopathy", "GUCY2D-related dominant retinopathy", "choroidal dystrophy, central areolar", "choroidal dystrophy, central areolar, 1", "GUCY2D central areolar choroidal dystrophy", "cone-rod dystrophy caused by mutation in GUCY2D", "central areolar choroidal dystrophy caused by mutation in GUCY2D"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "GUCY2D-related dominant retinopathy", "shortest_name_length": 4}
{"curie": "MONDO:0005294", "names": ["PAD", "pvd", "pvds", "artery block", "Blocked artery", "blocked artery", "artery occlusion", "artery occlusions", "arterial occlusion", "ARTERIAL OCCLUSION", "Arterial Occlusion", "Arterial occlusion", "Occlusion;arterial", "artery obstruction", "obstruction; artery", "Arterial occlusions", "Occlusion, Arterial", "artery obstructions", "arterial occlusions", "Arterial Occlusions", "artery; obstruction", "Occlusion of artery", "Arterial Obstruction", "arterial obstruction", "Obstruction of artery", "Peripheral Angiopathy", "Peripheral angiopathy", "peripheral angiopathy", "angiopathy; peripheral", "Angiopathy, Peripheral", "Arterial occlusion NOS", "peripheral; angiopathy", "peripheral angiopathies", "Peripheral Angiopathies", "Arterial disease of legs", "Arterial obstruction NOS", "Occlusion of artery, NOS", "Angiopathies, Peripheral", "Peripheral Artery Disease", "Peripheral angiopathy NOS", "Arterial flow obstruction", "Peripheral artery disease", "vascular occlusive disease", "Arterial Occlusive Disease", "Peripheral Artery Diseases", "Arterial occlusive disease", "occlusive arterial disease", "arterial occlusive disease", "arterial disease occlusive", "Peripheral angiopathy, NOS", "VASCULAR DISEASE OCCLUSIVE", "occlusive vascular disease", "Occlusive vascular disease", "vascular disease occlusive", "Artery Disease, Peripheral", "Disease, Peripheral Artery", "Obstruction of artery, NOS", "Occlusive arterial disease", "Occlusive Disease, Arterial", "Arterial Occlusive Diseases", "Peripheral vascular disease", "peripheral vascular disease", "Disease, Arterial Occlusive", "Diseases, Peripheral Artery", "Disease;peripheral vascular", "artery; disorder, occlusive", "Artery Diseases, Peripheral", "PERIPHERAL VASCULAR DISEASE", "Peripheral Vascular Disease", "Peripheral Arterial Disease", "peripheral arterial disease", "Peripheral arterial disease", "VASCULAR DISEASE PERIPHERAL", "arterial occlusive diseases", "vascular disease, peripheral", "Peripheral Vascular Disorder", "DISORDER PERIPHERAL VASCULAR", "Vascular disorder peripheral", "arterial diseases peripheral", "Disorder peripheral vascular", "VASCULAR DISORDER PERIPHERAL", "arterial obstructive disease", "Disease, Peripheral Arterial", "Peripheral Vascular Diseases", "Disease, Peripheral Vascular", "DISORDER VASCULAR PERIPHERAL", "Arterial Disease, Peripheral", "Peripheral vascular diseases", "disease, peripheral vascular", "obstructive arterial disease", "Peripheral vascular disorder", "peripheral vascular diseases", "PERIPHERAL VASCULAR DISORDER", "Peripheral Arterial Disorder", "peripheral vascular disorder", "Disorder vascular peripheral", "Peripheral Arterial Diseases", "Peripheral arterial stenosis", "Vascular Disease, Peripheral", "Arterial Obstructive Disease", "Diseases, Peripheral Vascular", "vascular; disorder, occlusive", "Obstructive Disease, Arterial", "Diseases, Peripheral Arterial", "Arterial Obstructive Diseases", "Disease, Arterial Obstructive", "Vascular Diseases, Peripheral", "Arterial Diseases, Peripheral", "Occlusion of artery (disorder)", "arterial occlusion (diagnosis)", "circulatory disorder peripheral", "Circulatory disorder peripheral", "Peripheral vascular disease NOS", "PERIPHERAL VASCULAR DISORDER NOS", "Peripheral vascular disorder NOS", "circulatory disorders peripheral", "Peripheral vascular disease, NOS", "peripheral blood vessel disorder", "peripheral vascular disease (PVD)", "PVD - Peripheral vascular disease", "Peripheral angiopathy (diagnosis)", "PVD (peripheral vascular disease)", "PVD - peripheral vascular disease", "Peripheral artery occlusive disease", "Peripheral arterial vascular disease", "Peripheral vascular disease (disorder)", "Peripheral arterial disease (disorder)", "peripheral arterial disease (diagnosis)", "peripheral vascular disease (diagnosis)", "Peripheral vascular disease unspecified", "Peripheral vascular disease, unspecified", "disease (or disorder); artery, occlusive", "disease (or disorder); vascular, occlusive", "disease (or disorder); peripheral, vascular", "peripheral vascular disease peripheral angiopathy", "peripheral angiopathy in diseases classified elsewhere", "Peripheral angiopathy in diseases classified elsewhere", "peripheral angiopathy in diseases classified elsewhere (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peripheral vascular disease", "shortest_name_length": 3}
{"curie": "UMLS:C4525297", "names": ["Gallbladder cancer", "stage 0 gallbladder cancer", "Stage 0 Gallbladder Cancer", "Stage 0 Gallbladder Cancer AJCC v8", "stage 0 gallbladder cancer AJCC v8", "stage 0 gallbladder carcinoma AJCC v8", "Stage 0 Gallbladder Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Gallbladder Cancer AJCC v8", "shortest_name_length": 18}
{"curie": "MONDO:0008939", "names": ["CHEGDD", "Small cerebellum", "Chiari 4 malformation", "Cerebellar hypoplasia", "Hypoplasia cerebellar", "cerebellum hypoplasia", "hypoplasia cerebellum", "cerebellar hypoplasia", "Cerebellar Hypoplasia", "hypoplasia cerebellar", "HYPOPLASIA CEREBELLAR", "hypoplasia; cerebellum", "Chiari IV malformation", "Hypoplastic cerebellum", "cerebellum; hypoplasia", "Hypoplasia of cerebellum", "Underdeveloped cerebellum", "Congenital small cerebellum", "isolated cerebellar agenesis", "Hypoplasia of the cerebellum", "subtotal absence of cerebellum", "Congenital Cerebellar Hypoplasia", "near total absence of cerebellum", "congenital cerebellar hypoplasia", "Congenital cerebellar hypoplasia", "congenital cerebellar Hypoplasia", "Congenital hypoplasia of cerebellum", "isolated cerebellar hypoplasia/agenesis", "Congenital cerebellar hypoplasia (disorder)", "CEREBELLAR HYPOPLASIA/ATROPHY, EPILEPSY, AND GLOBAL DEVELOPMENTAL DELAY", "cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated cerebellar hypoplasia/agenesis", "shortest_name_length": 6}
{"curie": "MONDO:0004274", "names": ["breast carcinosarcoma", "Breast Carcinosarcoma", "mixed type metaplastic breast cancer", "Mixed Epithelial/Mesenchymal Metaplastic Breast Carcinoma", "mixed epithelial/mesenchymal metaplastic breast carcinoma", "Breast Mixed Epithelial/Mesenchymal Metaplastic Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed epithelial/mesenchymal metaplastic breast carcinoma", "shortest_name_length": 21}
{"curie": "MONDO:0021335", "names": ["duodenal cancer", "Duodenal Cancer", "Cancer of Duodenum", "cancer of duodenum", "duodenal carcinoma", "duodenum carcinoma", "Duodenal Carcinoma", "carcinoma of duodenum", "Carcinoma of Duodenum", "Cancer of the Duodenum", "cancer of the duodenum", "Carcinoma of the Duodenum", "carcinoma of the duodenum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma of duodenum", "shortest_name_length": 15}
{"curie": "MONDO:0022685", "names": ["cerebellar agenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellar agenesis", "shortest_name_length": 19}
{"curie": "MONDO:0015841", "names": ["Uterus subseptus", "Subseptate Uteri", "uterus subseptus", "subseptus; uterus", "Subseptate Uterus", "uterus; subseptus", "Subseptate uterus", "Uterus, Subseptate", "Uterus, subseptate", "partial septate uterus", "Partial septate uterus", "subtotal septate uterus", "Subtotal septate uterus", "Incomplete Septate Uterus", "Septate Uterus, Incomplete", "Uterus subseptus (disorder)", "partial septate uterus (diagnosis)", "congenital abnormality of uterus septate partial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial septate uterus", "shortest_name_length": 16}
{"curie": "MONDO:0000044", "names": ["hereditary hypophosphatemic rickets"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary hypophosphatemic rickets", "shortest_name_length": 35}
{"curie": "UMLS:C0267896", "names": ["Gallbladder hydrops", "Gallbladder Hydrops", "Gallbladder Mucocele", "Gallbladder mucocele", "mucocele; gallbladder", "gallbladder; mucocele", "GALLBLADDER, MUCOCELE", "Gallbladder mucocoele", "Mucocele of gallbladder", "Mucocele of gallbladder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mucocele of gallbladder", "shortest_name_length": 19}
{"curie": "UMLS:C4054533", "names": ["Meningothelial Hamartoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meningothelial Hamartoma", "shortest_name_length": 24}
{"curie": "UMLS:C4330010", "names": ["Frontal Lobe and Parietal Lobe Ependymal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Frontal Lobe and Parietal Lobe Ependymal Tumor", "shortest_name_length": 46}
{"curie": "UMLS:C5669686", "names": ["Unresectable Hilar Cholangiocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Hilar Cholangiocarcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0018925", "names": ["Migraine;hemiplegic", "Migraine hemiplegic", "Hemiplegic migraine", "hemiplegic migraine", "migraine; hemiplegic", "Hemiplegic migraines", "hemiplegic; migraine", "hemiplegic migraines", "Hemiplegic migraine NOS", "hemiplegic migraine headache", "Hemiplegic migraine (disorder)", "Familial or sporadic hemiplegic migraine", "hemiplegic migraine headache (diagnosis)", "familial or sporadic hemiplegic migraine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial or sporadic hemiplegic migraine", "shortest_name_length": 19}
{"curie": "MONDO:0017730", "names": ["MLD, adult form", "arylsulfatase A deficiency, adult form", "metachromatic leukodystrophy, adult form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metachromatic leukodystrophy, adult form", "shortest_name_length": 15}
{"curie": "MONDO:0010068", "names": ["SEMDSP", "SPONASTRIME", "Sponastrime dysplasia", "Sponastrime Dysplasia", "sponastrime dysplasia", "SPONASTRIME DYSPLASIA", "SPONASTRIME dysplasia", "Sponastrime dysplasia (disorder)", "spondyloepimetaphyseal dysplasia Sponastrime type", "SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE", "spondyloepimetaphyseal dysplasia, Sponastrime type", "Spondyloepimetaphyseal dysplasia, sponastrime type", "Spondyloepimetaphyseal Dysplasia, Sponastrime Type", "Spondyloepimetaphyseal dysplasia, Sponastrime type", "spondyloepimetaphyseal dysplasia, sponastrime type", "spondylar and nasal alterations with striated metaphyses", "SPONDYLAR AND NASAL ALTERATIONS WITH STRIATED METAPHYSES", "Spondylar and nasal alterations with striated metaphyses", "Spondylar and nasal Alterations-Striated Metaphyses syndrome", "spondylar and nasal alterations-striated metaphyses syndrome", "SPONASTRIME (SPOndylar changes-NAsal anomaly-STRIated-MEtaphyses)", "short limb dwarfism-saddle nose-spinal alterations-metaphyseal striation syndrome", "Short Limb Dwarfism-Saddle Nose-Spinal Alterations-Metaphyseal Striation Syndrome", "short-limb dwarfism with saddle Nose, spinal alterations, and metaphyseal striation", "Short-Limb Dwarfism with Saddle Nose, Spinal Alterations, and Metaphyseal Striation", "SHORT-LIMB DWARFISM WITH SADDLE NOSE, SPINAL ALTERATIONS, AND METAPHYSEAL STRIATION", "short limb dwarfism with saddle nose, spinal alterations, and metaphyseal striation", "spondylar and nasal changes with triations of the metaphyses (SPONASTRIME) dysplasia", "spondylar and nasal changes with striations of the metaphyses (SPONASTRIME) dysplasia", "Spondylar and nasal changes with striations of the metaphyses (SPONASTRIME) dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepimetaphyseal dysplasia, sponastrime type", "shortest_name_length": 6}
{"curie": "UMLS:C1167791", "names": ["skin toxicity", "toxicity skin", "Skin toxicity", "skin toxicities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin toxicity", "shortest_name_length": 13}
{"curie": "MONDO:0011308", "names": ["FLNMS", "Fellman disease", "gracile syndrome", "Fellman syndrome", "FELLMAN SYNDROME", "GRACILE SYNDROME", "GRACILE syndrome", "GRACILE SYNDROME (disorder)", "Finnish lethal neonatal metabolic syndrome", "FINNISH LETHAL NEONATAL METABOLIC SYNDROME", "Finnish lactic acidosis with hepatic hemosiderosis", "Finnish, lactic acidosis with hepatic hemosiderosis", "Lactic Acidosis, Finnish, With Hepatic Hemosiderosis", "lactic acidosis, Finnish, with hepatic hemosiderosis", "LACTIC ACIDOSIS, FINNISH, WITH HEPATIC HEMOSIDEROSIS", "growth delay-aminoaciduria-cholestasis-iron overload-lactic acidosis-early death syndrome", "Growth delay-aminoaciduria-cholestasis-iron overload-lactic acidosis-early death syndrome", "Growth retardation, aminoaciduria, cholestasis, iron overload, lactic acidosis and early death", "Growth restriction-aminoaciduria-cholestasis-iron overload-lactic acidosis-early death syndrome", "growth restriction-aminoaciduria-cholestasis-iron overload-lactic acidosis-early death syndrome", "Growth retardation, amino aciduria, cholestasis, iron overload, lactic acidosis, and early death", "growth retardation, amino aciduria, cholestasis, iron overload, lactic acidosis, and early death", "GROWTH RETARDATION, AMINO ACIDURIA, CHOLESTASIS, IRON OVERLOAD, LACTIC ACIDOSIS, AND EARLY DEATH", "Growth retardation, amino aciduria, cholestasis, iron overload, lactic acidosis, and early death (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "GRACILE syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0032667", "names": ["EV5", "EPIDERMODYSPLASIA VERRUCIFORMIS, SUSCEPTIBILITY TO, 5", "epidermodysplasia verruciformis, susceptibility to, 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermodysplasia verruciformis, susceptibility to, 5", "shortest_name_length": 3}
{"curie": "MONDO:0011909", "names": ["CMTDID", "DI-CMTD", "Di-Cmtd", "MPZ Charcot-Marie-Tooth disease", "Charcot Marie Tooth disease dominant intermediate 3", "Charcot-Marie-Tooth disease dominant intermediate D", "Charcot-Marie-Tooth Disease, Dominant Intermediate D", "CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE D", "Charcot-Marie-Tooth disease, dominant intermediate D", "Charcot-Marie-Tooth disease caused by mutation in MPZ", "Charcot-Marie-Tooth neuropathy dominant intermediate D", "Charcot-Marie-Tooth neuropathy, dominant Intermediate D", "CHARCOT-MARIE-TOOTH NEUROPATHY, DOMINANT INTERMEDIATE D", "Charcot-Marie-Tooth Neuropathy, Dominant Intermediate D", "MPZ-related intermediate Charcot-Marie-Tooth neuropathy", "Charcot-Marie-Tooth disease dominant intermediate type D", "Charcot-Marie-Tooth disease, dominant Intermediate type D", "Charcot-Marie-Tooth disease autosomal dominant intermediate type D", "Autosomal dominant intermediate Charcot-Marie-Tooth disease type D", "autosomal dominant intermediate Charcot-Marie-Tooth disease type D", "Autosomal dominant intermediate Charcot-Marie-Tooth disease type D (disorder)", "Autosomal dominant intermediate Charcot-Marie-Tooth disease type D (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease dominant intermediate D", "shortest_name_length": 6}
{"curie": "UMLS:C0948158", "names": ["Pulmonary sepsis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pulmonary sepsis", "shortest_name_length": 16}
{"curie": "UMLS:C1335124", "names": ["Mouth Sarcoma", "Sarcoma of Mouth", "Oral Cavity Sarcoma", "Sarcoma of the Mouth", "sarcoma of oral cavity", "Sarcoma of Oral Cavity", "Sarcoma of the Oral Cavity", "sarcoma of oral cavity (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sarcoma of oral cavity", "shortest_name_length": 13}
{"curie": "MONDO:0002828", "names": ["Bartholin Gland Transitional Cell Carcinoma", "Bartholin gland transitional cell carcinoma", "Bartholin's Gland Transitional Cell Carcinoma", "Bartholin's gland transitional cell carcinoma", "major vestibular gland transitional cell carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bartholin gland transitional cell carcinoma", "shortest_name_length": 43}
{"curie": "UMLS:C3266101", "names": ["22q11 partial monosomy syndrome", "22q11 partial monosomy syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "22q11 partial monosomy syndrome", "shortest_name_length": 31}
{"curie": "MONDO:0030719", "names": ["DFNA82", "deafness, autosomal dominant 82", "DEAFNESS, AUTOSOMAL DOMINANT 82", "hearing loss, autosomal dominant 82"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal dominant 82", "shortest_name_length": 6}
{"curie": "UMLS:C1331536", "names": ["v.cava; occlusion", "Vena Cava Occlusion", "occlusion; vena cava"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vena Cava Occlusion", "shortest_name_length": 17}
{"curie": "MONDO:0013293", "names": ["MCOP6", "isolated microphthalmia 6", "microphthalmia, isolated 6", "MICROPHTHALMIA, ISOLATED 6", "isolated microphthalmia type 6", "PRSS56 isolated microphthalmia", "microphthalmia, isolated type 6", "posterior nonsyndromic microphthalmia", "MICROPHTHALMIA, POSTERIOR NONSYNDROMIC", "microphthalmia, posterior nonsyndromic", "isolated microphthalmia caused by mutation in PRSS56"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated microphthalmia 6", "shortest_name_length": 5}
{"curie": "MONDO:0012571", "names": ["CILD6", "primary ciliary dyskinesia 6", "Ciliary Dyskinesia, Primary, 6", "ciliary dyskinesia, primary, 6", "CILIARY DYSKINESIA, PRIMARY, 6", "NME8 primary ciliary dyskinesia", "primary ciliary dyskinesia type 6", "ciliary dyskinesia, primary, type 6", "primary ciliary dyskinesia caused by mutation in NME8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia 6", "shortest_name_length": 5}
{"curie": "MONDO:0006572", "names": ["ruber planus", "Ruber planus", "Lichen Planus", "Lichen planus", "LICHEN PLANUS", "lichen planus", "lichen; planus", "planus; lichen", "LP - Lichen planus", "Lichen Ruber Planus", "LICHEN RUBER PLANUS", "lichen ruber planus", "Lichen Rubra Planus", "Lichen, ruber planus", "lichen; ruber planus", "Wilson; lichen ruber", "lichen ruber; Wilson", "lichen, ruber planus", "Lichen planus (disorder)", "lichen; planus, of Wilson", "planus; lichen, of Wilson", "lichen planus (diagnosis)", "Lichen planus, unspecified", "ruber; lichen ruber planus", "planus; lichen ruber planus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lichen planus", "shortest_name_length": 12}
{"curie": "UMLS:C5420045", "names": ["Sinonasal Fibrosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Fibrosarcoma", "shortest_name_length": 22}
{"curie": "UMLS:C0027013", "names": ["METAPLASIA MYELOID", "metaplasia myeloid", "Metaplasia myeloid", "myeloid metaplasia", "MYELOID METAPLASIA", "Myeloid Metaplasia", "Myeloid metaplasia", "Myeloid Metaplasias", "MYELOID METAPLASIAS", "Metaplasia, myeloid", "myeloid; metaplasia", "metaplasia; myeloid", "metaplasia; myelogenous", "myelogenous; metaplasia", "Myeloid metaplasia (disorder)", "Myeloid metaplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myeloid Metaplasia", "shortest_name_length": 18}
{"curie": "UMLS:C1334235", "names": ["Intra-Abdominal Paraganglioma", "Paraganglioma of Intra-Abdominal Area", "Paraganglioma of the Intra-Abdominal Area"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intra-Abdominal Paraganglioma", "shortest_name_length": 29}
{"curie": "MONDO:0060585", "names": ["HMN9", "DHMN9", "distal hereditary motor neuropathy type IX", "distal hereditary motor neuronopathy type 9", "neuropathy, distal hereditary motor, type 9", "NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IX", "neuronopathy, distal hereditary motor, type 9", "neuronopathy, distal hereditary motor, type IX", "NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IX"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuronopathy, distal hereditary motor, type 9", "shortest_name_length": 4}
{"curie": "UMLS:C4683656", "names": ["B-Lymphoblastic Lymphoma by Ann Arbor Stage", "B Lymphoblastic Lymphoma by Ann Arbor Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B Lymphoblastic Lymphoma by Ann Arbor Stage", "shortest_name_length": 43}
{"curie": "MONDO:0010747", "names": ["XDP", "DYT3", "Lubag", "DYT-TAF1", "Dystonia 3", "Lubag Syndrome", "Lubag syndrome", "dystonia 3, torsion, X-linked", "Dystonia 3, Torsion, X-Linked", "DYSTONIA 3, TORSION, X-LINKED", "X-Linked Dystonia Parkinsonism", "X-Linked Dystonia-Parkinsonism", "X-linked dystonia parkinsonism", "X-linked dystonia Parkinsonism", "X-linked dystonia-parkinsonism", "DYSTONIA-PARKINSONISM, X-LINKED", "Dystonia-Parkinsonism, X-Linked", "dystonia-Parkinsonism, X-linked", "XDP - X-linked dystonia parkinsonism", "X-linked dystonia-parkinsonism/Lubag", "X-linked dystonia-Parkinsonism syndrome", "X-Linked Dystonia-Parkinsonism Syndrome", "X-linked dystonia parkinsonism (disorder)", "Torsion dystonia parkinsonism Filipino type", "TORSION DYSTONIA-PARKINSONISM, FILIPINO TYPE", "torsion dystonia-Parkinsonism, Filipino type", "Torsion Dystonia-Parkinsonism, Filipino Type", "X-linked torsion dystonia-Parkinsonism syndrome", "X-Linked Torsion Dystonia-Parkinsonism Syndrome", "X-linked torsion dystonia parkinsonism syndrome", "dystonia-Parkinsonism, X-linked, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked dystonia-parkinsonism", "shortest_name_length": 3}
{"curie": "MONDO:0007997", "names": ["MICROSPHEROPHAKIA WITH HERNIA", "Microspherophakia with hernia", "microspherophakia with hernia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microspherophakia with hernia", "shortest_name_length": 29}
{"curie": "UMLS:C0240371", "names": ["MOUTH MUCOUS MEMBRANE LEUKOPLAKIA", "Mouth Mucous Membrane Leukoplakia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mouth Mucous Membrane Leukoplakia", "shortest_name_length": 33}
{"curie": "MONDO:0011385", "names": ["LDD", "IDD", "Disk Degradation", "Disc Degradation", "disc degeneration", "Disc degeneration", "Degradation, Disk", "Disk Degradations", "Disc Degeneration", "Degradation, Disc", "degeneration disc", "Disc Degradations", "Disk Degeneration", "Disk Degenerations", "Degeneration, Disk", "Degeneration, Disc", "Disc Degenerations", "disc disease lumbar", "LUMBAR DISC DISEASE", "disease lumbar disc", "Lumbar disc disease", "Lumbar Disc Disease", "lumbar disc disease", "vertebral disc disease", "lumbar disc degeneration", "Degenerative Disc Disease", "Degenerative disc disease", "LUMBAR SPINE DISC DISEASE", "disc disease degenerative", "degenerative disc disease", "disc degenerative disease", "Degenerative Disc Diseases", "Disc Disease, Degenerative", "degenerative disc diseases", "intervertebral disc disease", "Degenerative disc disease NOS", "Degenerative disc disease, NOS", "Degenerated intervertebral disc", "intervertebral Disc Degeneration", "Intervertebral Disk Degeneration", "intervertebral disk degeneration", "Intervertebral disc degeneration", "Degenerative intervertebral disk", "degeneration disc intervertebral", "Degenerative intervertebral disc", "Intervertebral Disc Degeneration", "intervertebral disc degeneration", "intervertebral disc; degeneration", "Intervertebral Disk Degenerations", "Disk Degeneration, Intervertebral", "Intervertebral Disc Degenerations", "Disc Degeneration, Intervertebral", "Degeneration, Intervertebral Disc", "Degeneration, Intervertebral Disk", "degeneration; intervertebral disc", "cervical disc degenerative disease", "Vertebral Disc Degenerative Disease", "vertebral Disc degenerative disease", "degeneration of intervertebral disc", "Degeneration of intervertebral disc", "Degeneration of intervertebral disks", "Degeneration of intervertebral discs", "Intervertebral disc degeneration NOS", "Vertebral Disc Degenerative Disorder", "vertebral Disc degenerative disorder", "Degenerative intervertebral disc disease", "intervertebral Disc degenerative disease", "Degeneration of intervertebral disc, NOS", "Intervertebral Disc Degenerative Disease", "Intervertebral Disc Degenerative Disorder", "intervertebral Disc degenerative disorder", "intervertebral disk degenerative disorder", "LUMBAR DISC HERNIATION, SUSCEPTIBILITY TO", "intervertebral disc degenerative disorder", "LUMBAR DISC DEGENERATION, SUSCEPTIBILITY TO", "degenerative disorder of intervertebral disk", "Degeneration of intervertebral disc (disorder)", "degeneration of intervertebral disc (diagnosis)", "Degeneration of intervertebral disc, site unspecified", "disease (or disorder); intervertebral disc, lumbar, lumbosacral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intervertebral disc degenerative disorder", "shortest_name_length": 3}
{"curie": "MONDO:0013964", "names": ["DBA11", "Diamond-Blackfan anemia 11", "DIAMOND-BLACKFAN ANEMIA 11", "Diamond-Blackfan Anemia 11", "RPL26 Diamond-Blackfan anemia", "Diamond-Blackfan Anemia type 11", "RPL26-related Diamond-Blackfan anemia", "Diamond-Blackfan anemia caused by mutation in RPL26"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diamond-Blackfan anemia 11", "shortest_name_length": 5}
{"curie": "UMLS:C4687702", "names": ["Pericardial Synovial Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pericardial Synovial Sarcoma", "shortest_name_length": 28}
{"curie": "UMLS:C1336329", "names": ["urethra cancer stage II", "Urethra Cancer Stage II", "stage II urethral cancer", "Stage II Urethral Cancer", "Stage II Urethra Carcinoma", "stage II urethra carcinoma", "stage II urethral carcinoma", "Stage II Urethral Carcinoma", "stage II carcinoma of urethra", "Stage II Carcinoma of Urethra", "stage II urethral cancer AJCC v7", "Stage II Urethral Cancer AJCC v7", "stage II carcinoma of the urethra", "Stage II Carcinoma of the Urethra"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Urethral Cancer AJCC v7", "shortest_name_length": 23}
{"curie": "UMLS:C5206968", "names": ["Metastatic NMC", "Metastatic NUT Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic NUT Carcinoma", "shortest_name_length": 14}
{"curie": "MONDO:0024240", "names": ["Eccrine carcinoma", "eccrine carcinoma", "Eccrine Carcinoma", "Eccrine adenocarcinoma", "eccrine adenocarcinoma", "eccrine carcinoma of skin", "Eccrine carcinoma of skin", "eccrine carcinoma of the skin", "eccrine sweat gland carcinoma", "carcinoma of eccrine sweat gland", "eccrine sweat gland adenocarcinoma", "CARCINOMA, ECCRINE GLAND, MALIGNANT", "carcinoma, eccrine gland, malignant", "Eccrine carcinoma of skin (disorder)", "Eccrine carcinoma of skin (diagnosis)", "Eccrine adenocarcinoma (morphologic abnormality)", "eccrine adenocarcinoma (morphologic abnormality)", "skin neoplasm malignant adnexa with eccrine differentiation carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eccrine carcinoma", "shortest_name_length": 17}
{"curie": "MONDO:0008532", "names": ["Natal Teeth", "Natal teeth", "Natal Tooth", "natal tooth", "NATAL TEETH", "Natal tooth", "natal teeth", "Teeth, Natal", "Tooth, Natal", "neonatal tooth", "Neonatal teeth", "neonatal teeth", "Neonatal tooth", "teeth; neonatal", "Born with teeth", "neonatal; teeth", "Natal tooth (disorder)", "Teeth present at birth", "Natal teeth (disorder)", "teeth present AT birth", "TEETH PRESENT AT BIRTH", "teeth present at birth", "Teeth Present At Birth", "natal tooth (diagnosis)", "Neonatal tooth (disorder)", "neonatal tooth (diagnosis)", "natal tooth (physical finding)", "teeth present at birth (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "teeth present at birth", "shortest_name_length": 11}
{"curie": "MONDO:0016000", "names": ["familial isolated hypoparathyroidism due to impaired PTH secretion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial isolated hypoparathyroidism due to impaired PTH secretion", "shortest_name_length": 66}
{"curie": "MONDO:0024506", "names": ["AOS", "AOS1", "Adams Oliver syndrome", "Adams-Oliver syndrome", "ADAMS-OLIVER SYNDROME 1", "Adams-Oliver syndrome 1", "Scalp and head syndrome", "ARHGAP31 Adams-Oliver syndrome", "Scalp defects with ectrodactyly", "Congenital defect of skull and scalp", "Absence defect of limbs, scalp, and skull", "absence defect of limbs, scalp, and skull", "ABSENCE DEFECT OF LIMBS, SCALP, AND SKULL", "Familial aplasia cutis congenita of the scalp", "Adams-Oliver syndrome caused by mutation in ARHGAP31", "congenital scalp defects with distal limb reduction anomalies", "Aplasia Cutis Congenita With Terminal Transverse Limb Defects", "APLASIA CUTIS CONGENITA WITH TERMINAL TRANSVERSE LIMB DEFECTS", "CONGENITAL SCALP DEFECTS WITH DISTAL LIMB REDUCTION ANOMALIES", "aplasia cutis congenita with terminal transverse limb defects", "Congenital Scalp Defects With Distal Limb Reduction Anomalies", "aplasia cutis congenita, congenital heart defect, and frontonasal cysts", "Aplasia Cutis Congenita, Congenital Heart Defect, And Frontonasal Cysts", "APLASIA CUTIS CONGENITA, CONGENITAL HEART DEFECT, AND FRONTONASAL CYSTS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adams-Oliver syndrome 1", "shortest_name_length": 3}
{"curie": "UMLS:C0205882", "names": ["Parvovirus infection", "Parvovirus Infection", "infection parvovirus", "parvovirus infection", "Parvovirus infections", "Parvovirus Infections", "Infection, Parvovirus", "Infections, Parvovirus", "infection; viral, parvovirus", "Parvovirus infection (disorder)", "Parvovirus infection, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infections, Parvovirus", "shortest_name_length": 20}
{"curie": "UMLS:C4727429", "names": ["Refractory Malignant Central Nervous System Neoplasm", "Refractory Primary Malignant Central Nervous System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Primary Malignant Central Nervous System Neoplasm", "shortest_name_length": 52}
{"curie": "MONDO:0100152", "names": ["DKC1-related disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DKC1-related disorder", "shortest_name_length": 21}
{"curie": "UMLS:C0454643", "names": ["Word finding difficulty", "Word-finding difficulties", "Lexical retrieval deficit", "Word finding difficulty (disorder)", "Word finding difficulty (diagnosis)", "developmental disorder - language impairment word finding difficulty"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Word finding difficulty (disorder)", "shortest_name_length": 23}
{"curie": "UMLS:C4521625", "names": ["Stage III Sinonasal Cancer AJCC v8", "Stage III Sinonasal Carcinoma AJCC v8", "Stage III Nasal Cavity and Paranasal Sinus Cancer", "Stage III Nasal Cavity and Paranasal Sinus Cancer AJCC v8", "Stage III Nasal Cavity and Paranasal Sinus Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Nasal Cavity and Paranasal Sinus Cancer AJCC v8", "shortest_name_length": 34}
{"curie": "UMLS:C4524732", "names": ["Pathologic Stage IIA Gastroesophageal Junction Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IIA Gastroesophageal Junction Adenocarcinoma AJCC v8", "shortest_name_length": 69}
{"curie": "MONDO:0004830", "names": ["Fascitis", "FASCITIS", "Fasciitis", "fasciitis", "FASCIITIS", "Fascitides", "Fasciitides", "Fasciitis NOS", "Fasciitis, NOS", "fasciitis; diffuse", "diffuse; fasciitis", "FASCIITIS, DIFFUSE", "fascia inflammation", "fasciitis (disease)", "fascia; inflammation", "Fasciitis (disorder)", "inflammation; fascia", "fasciitis (diagnosis)", "Fasciitis, unspecified", "inflammation of fascia", "Inflammation of the fascia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fasciitis", "shortest_name_length": 8}
{"curie": "UMLS:C5444421", "names": ["AHUS4", "Atypical Hemolytic Uremic Syndrome-4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypical Hemolytic Uremic Syndrome-4", "shortest_name_length": 5}
{"curie": "MONDO:0004897", "names": ["hypotropia", "Hypotropia", "sunset sign", "Sunset Sign", "hyop - Hypotropia", "Hypotropia (disorder)", "hypotropia (diagnosis)", "deviation downward eye", "EYE DEVIATION, DOWNWARD", "Downward Ocular Deviation", "downward ocular deviation", "Downward deviation of eyes", "downward deviation of eyes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotropia", "shortest_name_length": 10}
{"curie": "MONDO:0010127", "names": ["Thymic Neoplasia", "THYMIC NEOPLASIA", "thymic neoplasia", "thymoma, familial", "Thymoma, Familial", "THYMOMA, FAMILIAL", "hereditary thymoma (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thymoma, familial", "shortest_name_length": 16}
{"curie": "MONDO:0017636", "names": ["Hp-HA syndrome", "hemiparkinsonism-hemiatrophy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemiparkinsonism-hemiatrophy syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C1336758", "names": ["Tobacco-Related Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tobacco-Related Carcinoma", "shortest_name_length": 25}
{"curie": "UMLS:C5555072", "names": ["Peripheral Atypical Cartilaginous Tumor", "Secondary Peripheral Atypical Cartilaginous Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary Peripheral Atypical Cartilaginous Tumor", "shortest_name_length": 39}
{"curie": "MONDO:0010483", "names": ["MRX98", "XLID98", "X-linked mental retardation 98", "MENTAL RETARDATION, X-LINKED 98", "mental retardation, X-linked 98", "mental retardation, X-linked type 98", "intellectual disability, X-linked 98", "intellectual disability, X-linked type 98", "X-linked intellectual disability Cantagrel type", "X-linked intellectual disability, Cantagrel type", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 98", "non-syndromic X-linked intellectual disability 98", "X-linked intellectual disability Cantagrel type (disorder)", "X-linked intellectual disability Cantagrel type (diagnosis)", "intellectual developmental disorder, X-linked 98, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability, Cantagrel type", "shortest_name_length": 5}
{"curie": "UMLS:C5206448", "names": ["Stage III Cervical Cancer FIGO 2018", "Stage III Cervical Carcinoma FIGO 2018"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Cervical Cancer FIGO 2018", "shortest_name_length": 35}
{"curie": "UMLS:C0332712", "names": ["Spiral", "[Q] Spiral", "Linear spiral", "spiral fracture", "Spiral Fracture", "Spiral fracture", "Spiral Fractures", "Torsion Fracture", "Fracture, spiral", "Fracture, Spiral", "Fractures, Spiral", "Torsion Fractures", "Fracture, Torsion", "Fractures, Torsion", "Fracture, spiral (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fracture, spiral", "shortest_name_length": 6}
{"curie": "UMLS:C1275265", "names": ["Dermal neurothekeoma", "Dermal nerve sheath myxoma", "Dermal Nerve Sheath Myxoma", "Myxoid Variant of Neurothekeoma", "Classic Variant of Neurothekeoma", "Dermal nerve sheath myxoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dermal nerve sheath myxoma", "shortest_name_length": 20}
{"curie": "MONDO:0015751", "names": ["Berant syndrome", "Capra-DeMarco syndrome", "Capra DeMarco syndrome", "Capra DeMarco syndrome (disorder)", "Familial scaphocephaly-radioulnar synostosis syndrome", "familial scaphocephaly-radioulnar synostosis syndrome", "Familial scaphocephaly with radioulnar synostosis syndrome", "Craniosynostosis, hydrocephalus, Arnold Chiari I malformation, radioulnar synostosis", "craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome", "Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0015185", "names": ["Intestinal polyposis syndrome", "Intestinal Polyposis Syndrome", "intestinal polyposis syndrome", "Intestinal polyposis syndrome (disorder)", "intestinal polyposis syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intestinal polyposis syndrome", "shortest_name_length": 29}
{"curie": "UMLS:C5417748", "names": ["TA-TMA", "Transplant-Associated Thrombotic Microangiopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transplant-Associated Thrombotic Microangiopathy", "shortest_name_length": 6}
{"curie": "MONDO:0001901", "names": ["IgG Deficiency", "selective deficiency of IgG", "Selective deficiency of IgG", "selective IgG immunodeficiency", "Selective IgG Immunodeficiency", "selective IgG deficiency disease", "selective IgG subclass deficiency", "Immunoglobin G subclass deficiency", "selective immunoglobulin G deficiency", "Selective immunoglobulin G deficiency", "selective Immunoglobulin G subclass deficiency", "Selective Immunoglobulin G Subclass Deficiency", "Selective Immunoglobulin G Subclass deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "selective IgG subclass deficiency", "shortest_name_length": 14}
{"curie": "UMLS:C2750413", "names": ["Cap Myopathy, Tpm2-Related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cap Myopathy, Tpm2-Related", "shortest_name_length": 26}
{"curie": "MONDO:0009716", "names": ["Richieri Costa-da Silva syndrome", "Richieri Costa Da Silva syndrome", "Tibial hemimelia-split hand-foot syndrome", "Richieri Costa-da Silva syndrome (disorder)", "Richieri Costa-da Silva syndrome (diagnosis)", "MYOTONIA WITH SKELETAL ABNORMALITIES AND MENTAL RETARDATION", "Myotonia with Skeletal Abnormalities and Mental Retardation", "myotonia with skeletal abnormalities and mental retardation", "myotonia-intellectual disability-skeletal anomalies syndrome", "Myotonia-intellectual disability-skeletal anomalies syndrome", "Myotonia, intellectual disability, skeletal anomalies syndrome", "myotonia with skeletal abnormalities and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Richieri Costa-da Silva syndrome", "shortest_name_length": 32}
{"curie": "MONDO:0015435", "names": ["R19", "Ring 19", "(19)r syndrome", "r(19) syndrome", "Chromosome 19 ring", "Ring chromosome 19", "ring chromosome 19", "chromosome 19 ring", "Ring chromosome type 19", "Ring chromosome 19 syndrome", "ring chromosome 19 syndrome", "chromosome 19 ring syndrome", "Ring chromosome 19 syndrome (disorder)", "Ring chromosome 19 syndrome (diagnosis)", "anomaly of chromosome pair ring chromosome 19 syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ring chromosome 19", "shortest_name_length": 3}
{"curie": "MONDO:0006763", "names": ["Duplay", "DUPLAY DISEASE", "shoulder frozen", "Frozen Shoulder", "frozen shoulder", "FROZEN SHOULDER", "Frozen shoulder", "SHOULDER, FROZEN", "frozen; shoulder", "frozen shoulders", "Duplay; bursitis", "shoulder; frozen", "bursitis; Duplay", "Frozen Shoulders", "Shoulder, Frozen", "Subdeltoid bursitis", "adhesive capsulitis", "subdeltoid bursitis", "subdeltoid; bursitis", "BURSITIS, SUBDELTOID", "bursitis; subdeltoid", "Duplay; periarthritis", "periarthritis; Duplay", "periarthritis shoulder", "shoulder; periarthritis", "SHOULDER, PERIARTHRITIS", "periarthritis; shoulder", "BURSITIS, SCAPULOHUMERAL", "scapulohumeral; bursitis", "Frozen shoulder syndrome", "frozen shoulder syndrome", "bursitis; scapulohumeral", "Periarthritis of shoulder", "periarthritis of shoulder", "Pericapsulitis of shoulder", "shoulder adhesive capsulitis", "SHOULDER, BURSITIS, ADHESIVE", "Shoulder Adhesive Capsulitis", "SHOULDER ADHESIVE CAPSULITIS", "adhesive capsulitis shoulder", "Adhesive Capsulitis, Shoulder", "Capsulitis, Shoulder Adhesive", "adhesions-capsulitis,shoulder", "Duplay periarthritis syndrome", "capsulitis; adhesive, shoulder", "adhesive; capsulitis, shoulder", "SHOULDER, TENDINITIS, ADHESIVE", "adhesive; tendinitis, shoulder", "SHOULDER, CAPSULITIS, ADHESIVE", "tendinitis; adhesive, shoulder", "Shoulder Adhesive Capsulitides", "Subdeltoid bursitis (disorder)", "Capsulitides, Shoulder Adhesive", "adhesive capsulitis of shoulder", "Duplay's periarthritis syndrome", "Adhesive Capsulitides, Shoulder", "Adhesive capsulitis of shoulder", "SHOULDER, PERITENDINITIS, ADHESIVE", "Adhesive Capsulitis of the Shoulder", "periarthritis of shoulder (diagnosis)", "Adhesive capsulitis of shoulder (disorder)", "adhesive capsulitis of shoulder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frozen shoulder", "shortest_name_length": 6}
{"curie": "UMLS:C2700620", "names": ["Anorectal Infection", "Anorectal infection", "Anorectal infection (diagnosis)", "intestinal infections anorectal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anorectal infection", "shortest_name_length": 19}
{"curie": "UMLS:C0476201", "names": ["Axonotmeses", "axonotmesis", "Axonotmesis", "Axonotmesis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Axonotmesis", "shortest_name_length": 11}
{"curie": "MONDO:0004572", "names": ["Cyclothymia", "cyclothymia", "Cycloid personality", "cycloid personality", "cyclothymic disorder", "Cyclothymic Disorder", "Cyclothymic disorder", "CYCLOTHYMIC DISORDER", "Disorder cyclothymic", "cyclothymia disorder", "affective personality", "disorder; cyclothymic", "Affective personality", "cyclothymic; disorder", "Disorder, Cyclothymic", "cyclothymic disorders", "Cyclothymic Disorders", "Cyclothymia (disorder)", "Cyclothymic Personality", "Cyclothymic personality", "cyclothymic personality", "Personality, Cyclothymic", "Cyclothymic Personalities", "Unstable personality trait", "Affective personality trait", "Cyclothymic personality trait", "affective personality disorder", "Tends to be unstable in affect", "Affective personality disorder", "personality disorder; affective", "affective; personality disorder", "cyclothymic disorder (diagnosis)", "Cyclothymic personality disorder", "personality disorder; cyclothymic", "cyclothymic; personality disorder", "Affective personality trait (finding)", "affective personality disorder (diagnosis)", "Affective personality disorder, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cyclothymic disorder", "shortest_name_length": 11}
{"curie": "UMLS:C0948087", "names": ["hematoma infection", "Hematoma infection", "Haematoma infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hematoma infection", "shortest_name_length": 18}
{"curie": "MONDO:0009625", "names": ["DMJDS1", "MISSBC", "Microcephaly with spastic quadriplegia", "microcephaly with spastic quadriplegia", "Recessive microcephaly with spastic quadriplegia", "recessive microcephaly with spastic quadriplegia", "diencephalic-mesencephalic junction dysplasia syndrome 1", "DIENCEPHALIC-MESENCEPHALIC JUNCTION DYSPLASIA SYNDROME 1", "microcephaly, seizures, spasticity, and brain calcifications", "MICROCEPHALY, SEIZURES, SPASTICITY, AND BRAIN CALCIFICATIONS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diencephalic-mesencephalic junction dysplasia syndrome 1", "shortest_name_length": 6}
{"curie": "MONDO:0012869", "names": ["MRD22", "CHROMOSOME 1qter DELETION SYNDROME", "chromosome 1Qter deletion syndrome", "Chromosome 1qter Deletion Syndrome", "chromosome 1Q43-q44 deletion syndrome", "Chromosome 1q43-Q44 Deletion Syndrome", "CHROMOSOME 1q43-q44 DELETION SYNDROME", "autosomal dominant mental retardation 22", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 22", "mental retardation, autosomal dominant 22", "autosomal dominant intellectual disability 22", "mental retardation, autosomal dominant type 22", "intellectual disability, autosomal dominant 22", "intellectual disability, autosomal dominant type 22", "autosomal dominant intellectual developmental disorder 22", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 22", "autosomal dominant non-syndromic intellectual disability 22", "ZBTB18 autosomal dominant non-syndromic intellectual disability", "autosomal dominant non-syndromic intellectual disability caused by mutation in ZBTB18"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 22", "shortest_name_length": 5}
{"curie": "MONDO:0013786", "names": ["RP64", "CORD16", "CONE-ROD DYSTROPHY 16", "cone-rod dystrophy 16", "RETINITIS PIGMENTOSA 64", "retinitis pigmentosa 64", "C8orf37 cone-rod dystrophy", "cone-rod dystrophy type 16", "retinal dystrophy with early macular involvement", "cone-rod dystrophy caused by mutation in C8orf37"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cone-rod dystrophy 16", "shortest_name_length": 4}
{"curie": "MONDO:0004146", "names": ["Mixed meningioma", "mixed meningioma", "Mixed Meningioma", "mixed; meningioma", "meningioma; mixed", "Transitional Meningioma", "Transitional meningioma", "transitional meningioma", "Transitional Meningiomas", "transitional; meningioma", "meningioma; transitional", "Meningioma, Transitional", "Meningiomas, Transitional", "transitional (mixed) meningioma", "Transitional (Mixed) Meningioma", "Transitional meningioma (morphologic abnormality)", "transitional meningioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transitional meningioma", "shortest_name_length": 16}
{"curie": "MONDO:0009330", "names": ["malignant hemangiopericytoma", "Malignant hemangiopericytoma", "Malignant Hemangiopericytoma", "Hemangiopericytoma, Malignant", "hemangiopericytoma, malignant", "HEMANGIOPERICYTOMA, MALIGNANT", "Hemangiopericytoma, malignant", "Malignant haemangiopericytoma", "Haemangiopericytoma, malignant", "Malignant hemangiopericytoma NOS", "Malignant Hemangiopericytoma NOS", "Malignant haemangiopericytoma NOS", "malignant hemangiopericytoma (diagnosis)", "Malignant hemangiopericytoma stage unspecified", "Malignant haemangiopericytoma stage unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemangiopericytoma, malignant", "shortest_name_length": 28}
{"curie": "MONDO:0005546", "names": ["FMS", "fms", "Fibro", "Fibrositis", "FIBROSITIS", "fibrositis", "FIBROMYALGIA", "MPD syndrome", "mpd syndrome", "Fibromyalgia", "Fibrositides", "fibromyalgia", "Fibromyositis", "FIBROMYOSITIS", "fibromyalgias", "fibromyositis", "Fibromyalgias", "Fibrositis, NOS", "fibromyalgia (FM)", "Fibromyalgia, NOS", "Fibromyositis NOS", "Fibromyositis, NOS", "fibromyalgia (FMS)", "muscular rheumatism", "Muscular rheumatism", "Muscular Rheumatism", "RHEUMATISM, TENSION", "Rheumatism, Muscular", "Fibrositis (disorder)", "fibromyalgia syndrome", "syndrome fibromyalgia", "Fibromyalgia syndrome", "Fibromyalgia Syndrome", "fibrositis (diagnosis)", "Fibromyalgia (disorder)", "fibromyalgia (diagnosis)", "Fibromyositis (disorder)", "pain syndrome myofascial", "Myofascial pain syndrome", "Fibromyositis (diagnosis)", "MPS - myofascial pain syndrome", "Muscular rheumatism (disorder)", "Diffuse Myofascial Pain Syndrome", "Diffuse myofascial pain syndrome", "Myofascial trigger point syndrome", "Myofascial Pain Syndrome, Diffuse", "fibromyositis fibromyalgia syndrome", "Fibromyositis Fibromyalgia Syndrome", "Fibromyalgia Fibromyositis Syndrome", "Myofascial pain syndrome (disorder)", "Fibromyalgia-Fibromyositis Syndrome", "Myofacial pain dysfunction syndrome", "inflammatory myopathy fibromyositis", "Fibromyositis-Fibromyalgia Syndrome", "Myofascial pain dysfunction syndrome", "Fibromyalgia-Fibromyositis Syndromes", "Syndrome, Fibromyositis-Fibromyalgia", "Syndrome, Fibromyalgia-Fibromyositis", "myofascial pain dysfunction syndrome", "Fibromyositis-Fibromyalgia Syndromes", "Syndromes, Fibromyalgia-Fibromyositis", "Syndromes, Fibromyositis-Fibromyalgia", "MPDS - Myofacial pain dysfunction syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibromyalgia", "shortest_name_length": 3}
{"curie": "MONDO:0030491", "names": ["IMD91", "IMMUNODEFICIENCY 91 AND HYPERINFLAMMATION", "immunodeficiency 91 and hyperinflammation", "immunodeficiency, autosomal recessive, due to ZNFX1 deficiency:"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 91 and hyperinflammation", "shortest_name_length": 5}
{"curie": "UMLS:C0151824", "names": ["BILIARY PAIN", "Pain biliary", "PAIN BILIARY", "Biliary pain", "biliary pain", "Biliary colic", "Hepatic colic", "biliary colic", "Colic;biliary", "Biliary Colic", "Colic biliary", "COLIC BILIARY", "colic biliary", "BILIARY COLIC", "bilious; colic", "colic; bilious", "gallbladder pain", "Gallbladder pain", "Gallbladder Pain", "pain gallbladder", "Pain;gallbladder", "GALL BLADDER PAIN", "bladder gall pain", "gall bladder pain", "gallbladder; colic", "colic; gallbladder", "Biliary colic symptom", "Biliary colic (finding)", "Gallbladder pain (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Biliary Colic", "shortest_name_length": 12}
{"curie": "MONDO:0001438", "names": ["lung; fibrosis, postinflammatory", "fibrosis; lung, postinflammatory", "Postinflammatory pulmonary fibrosis", "postinflammatory pulmonary fibrosis", "post-inflammatory pulmonary fibrosis", "Post-inflammatory pulmonary fibrosis", "Post inflammatory pulmonary fibrosis", "Pulmonary fibrosis (post inflammatory)", "Post-inflammatory pulmonary fibrosis (disorder)", "postinflammatory pulmonary fibrosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postinflammatory pulmonary fibrosis", "shortest_name_length": 32}
{"curie": "UMLS:C4684861", "names": ["Recurrent Malignant Glioma", "Recurrent High-Grade Glioma", "Recurrent High Grade Glioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Malignant Glioma", "shortest_name_length": 26}
{"curie": "MONDO:0012797", "names": ["OTSC8", "Otosclerosis 8", "OTOSCLEROSIS 8", "otosclerosis 8", "OTOSCLEROSIS 8 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "otosclerosis 8", "shortest_name_length": 5}
{"curie": "UMLS:C0280318", "names": ["oropharynx lymphoepithelioma", "Oropharyngeal lymphepithelioma", "oropharyngeal lymphoepithelioma", "Oropharyngeal lymphoepithelioma", "Oropharyngeal Lymphoepithelioma", "lymphoepithelioma, oropharyngeal", "Oropharyngeal Undifferentiated Carcinoma", "Undifferentiated Oropharyngeal Throat Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oropharyngeal lymphepithelioma", "shortest_name_length": 28}
{"curie": "UMLS:C1336115", "names": ["Stage IA Gastric Cancer", "gastric cancer stage IA", "stage IA gastric cancer", "Gastric Cancer Stage IA", "stage IA gastric carcinoma", "Gastric Carcinoma Stage IA", "stage IA stomach carcinoma", "Stomach Carcinoma Stage IA", "stomach carcinoma stage IA", "Stage IA Stomach Carcinoma", "gastric carcinoma stage IA", "Stage IA Gastric Carcinoma", "carcinoma of stomach stage IA", "Carcinoma of Stomach Stage IA", "stage IA carcinoma of stomach", "Stage IA Carcinoma of Stomach", "stage IA gastric cancer AJCC v7", "Stage IA Gastric Cancer AJCC v7", "Stage IA Carcinoma of the Stomach", "Carcinoma of the Stomach Stage IA", "Stage IA Gastric (Stomach) Cancer", "stage IA carcinoma of the stomach", "carcinoma of the stomach stage IA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Gastric Carcinoma", "shortest_name_length": 23}
{"curie": "MONDO:0030843", "names": ["MMRCS4", "MISMATCH REPAIR CANCER SYNDROME 4", "mismatch repair cancer syndrome 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mismatch repair cancer syndrome 4", "shortest_name_length": 6}
{"curie": "MONDO:0006149", "names": ["Clear cell cystadenoma", "clear cell papillary cystadenoma", "Clear Cell Papillary Cystadenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "clear cell papillary cystadenoma", "shortest_name_length": 22}
{"curie": "MONDO:0034150", "names": ["idiopathic gastroparesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic gastroparesis", "shortest_name_length": 24}
{"curie": "UMLS:C3272527", "names": ["Small Intestinal Angiosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Intestinal Angiosarcoma", "shortest_name_length": 29}
{"curie": "UMLS:C4744755", "names": ["Thyroid Gland Benign Vascular Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Benign Vascular Neoplasm", "shortest_name_length": 38}
{"curie": "MONDO:0012587", "names": ["Hyt7", "HYT7", "hypertension, essential, susceptibility to, 7", "HYPERTENSION, ESSENTIAL, SUSCEPTIBILITY TO, 7", "hypertension, essential, susceptibility to, type 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertension, essential, susceptibility to, 7", "shortest_name_length": 4}
{"curie": "UMLS:C1142560", "names": ["Cytomegalovirus infection reactivation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cytomegalovirus infection reactivation", "shortest_name_length": 38}
{"curie": "UMLS:C1333816", "names": ["Giant Fibrovascular Esophagus Polyp", "Giant Fibrovascular Esophageal Polyp", "Giant Fibrovascular Polyp of Esophagus", "Giant Fibrovascular Polyp of the Esophagus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Giant Fibrovascular Esophageal Polyp", "shortest_name_length": 35}
{"curie": "MONDO:0006883", "names": ["PANCOAST TUMOR", "pancoast tumor", "Pancoast Tumor", "Pancoast tumor", "Pancoast tumour", "pancoast tumors", "Tumor, Pancoast", "pancoast tumour", "tumor; Pancoast", "Pancoast; tumor", "Pancoast's Tumor", "Pancoast's tumor", "pancoast's tumor", "Pancoast's tumour", "pancoast's tumour", "Pancoast's syndrome", "superior sulcus tumor", "Superior sulcus tumor", "superior sulcus tumour", "pulmonary sulcus tumor", "Superior sulcus tumour", "Pancoast tumor of lung", "pulmonary sulcus tumour", "Pancoast tumor (disorder)", "malignant Superior Sulcus tumor", "malignant Superior sulcus tumor", "Malignant Superior Sulcus Tumor", "malignant Superior Sulcus tumour", "Pancoast tumor of lung (diagnosis)", "superior pulmonary sulcus syndrome", "Malignant Superior Sulcus Neoplasm", "Superior pulmonary sulcus syndrome", "malignant superior sulcus neoplasm", "malignant Superior sulcus neoplasm", "malignant pulmonary sulcus neoplasm", "malignant Superior sulcus lung tumor", "pulmonary sulcus neoplasm, malignant", "Malignant Superior Sulcus Lung Tumor", "malignant Superior sulcus tumor of lung", "Malignant Superior Sulcus Lung Neoplasm", "Malignant Superior Sulcus Tumor of Lung", "malignant Superior sulcus lung neoplasm", "Malignant Superior Sulcus Neoplasm of Lung", "malignant Superior sulcus neoplasm of lung", "malignant Superior sulcus tumor of the lung", "Malignant Superior Sulcus Tumor of the Lung", "Malignant Superior Sulcus Neoplasm of the Lung", "malignant Superior sulcus neoplasm of the lung", "superior pulmonary sulcus syndrome (disorder) [ambiguous]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant superior sulcus neoplasm", "shortest_name_length": 14}
{"curie": "UMLS:C1517555", "names": ["Gliomatosis Cerebri Type I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gliomatosis Cerebri Type I", "shortest_name_length": 26}
{"curie": "UMLS:C1332054", "names": ["AIDS-Related Pelvic Inflammatory Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Pelvic Inflammatory Disease", "shortest_name_length": 40}
{"curie": "UMLS:C4744521", "names": ["Temporal Lobe Anaplastic Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Temporal Lobe Anaplastic Astrocytoma", "shortest_name_length": 36}
{"curie": "MONDO:0015063", "names": ["Duodenal Neuroendocrine Tumor", "duodenal neuroendocrine tumor", "Duodenal neuroendocrine tumor", "Duodenal neuroendocrine tumour", "duodenal neuroendocrine tumor, well differentiated, low or intermediate grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "duodenal neuroendocrine tumor, well differentiated, low or intermediate grade", "shortest_name_length": 29}
{"curie": "UMLS:C1336043", "names": ["Spinal Cord Hamartoma", "Hamartoma of Spinal Cord", "Hamartoma of the Spinal Cord"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spinal Cord Hamartoma", "shortest_name_length": 21}
{"curie": "UMLS:C2697519", "names": ["Grade 2 Diffuse Follicular Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade 2 Diffuse Follicular Lymphoma", "shortest_name_length": 35}
{"curie": "MONDO:0019903", "names": ["R2", "Ring 2", "rose cluster 2", "ROSE Cluster 2", "Ring chromosome 2", "ring chromosome 2", "chromosome 2 ring", "Ring chromosome type 2", "Ring chromosome 2 syndrome", "Ring chromosome 2 syndrome (disorder)", "Ring chromosome 2 syndrome (diagnosis)", "anomaly of chromosome pair ring chromosome 2 syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ring chromosome 2", "shortest_name_length": 2}
{"curie": "MONDO:0007446", "names": ["DERMATOSIS PAPULOSA NIGRA", "Dermatosis Papulosa Nigra", "Dermatosis papulosa nigra", "dermatosis papulosa nigra", "dermatosis; papulosa nigra", "papulosa nigra; dermatosis", "Dermatosis papulosa nigra (disorder)", "dermatosis papulosa nigra (diagnosis)", "dermatosis papulosa nigra (morphologic abnormality)", "Dermatosis papulosa nigra (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermatosis papulosa nigra", "shortest_name_length": 25}
{"curie": "UMLS:C1334591", "names": ["Malignant Tumor of Inferior Vena Cava", "Malignant Inferior Vena Cava Neoplasm", "Malignant Neoplasm of Inferior Vena Cava", "Malignant Tumor of the Inferior Vena Cava", "Malignant Neoplasm of the Inferior Vena Cava"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Inferior Vena Cava Neoplasm", "shortest_name_length": 37}
{"curie": "MONDO:0003913", "names": ["Choroid Mixed Cell Melanoma", "choroid mixed cell melanoma", "optic choroid mixed cell uveal melanoma", "mixed cell uveal melanoma of optic choroid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choroid mixed cell melanoma", "shortest_name_length": 27}
{"curie": "UMLS:C1609512", "names": ["Vulvovaginal mycotic infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvovaginal mycotic infection", "shortest_name_length": 30}
{"curie": "MONDO:0003707", "names": ["distal bile duct cancer", "Distal Bile Duct Carcinoma", "distal bile duct carcinoma", "distal biliary tract carcinoma", "carcinoma of distal biliary tract", "carcinoma of the distal biliary tract", "carcinoma of the Distal biliary tract", "Extrahepatic (Distal) Bile Duct Cancer", "extrahepatic (distal) bile duct cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal biliary tract carcinoma", "shortest_name_length": 23}
{"curie": "UMLS:C1707449", "names": ["combined thymoma", "composite thymoma", "Combined Thymic Carcinoma", "Combined Thymic Epithelial Tumor", "combined thymic epithelial tumor", "composite thymoma-thymic carcinoma", "Composite Thymoma-Thymic Carcinoma", "combined thymic epithelial neoplasm", "Combined Thymic Epithelial Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Combined Thymic Epithelial Neoplasm", "shortest_name_length": 16}
{"curie": "MONDO:0022938", "names": ["deafness goiter stippled epiphyses"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness goiter stippled epiphyses", "shortest_name_length": 34}
{"curie": "MONDO:0002606", "names": ["Epithelioid Angiomyolipoma", "Epithelioid angiomyolipoma", "epithelioid type angiomyolipoma", "Epithelioid Type Angiomyolipoma", "Epithelioid angiomyolipoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epithelioid type angiomyolipoma", "shortest_name_length": 26}
{"curie": "UMLS:C4521797", "names": ["Stage IV Gastric (Stomach) Cancer", "Postneoadjuvant Therapy Stage IV Gastric Cancer AJCC v8", "Postneoadjuvant Therapy Stage IV Gastric Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postneoadjuvant Therapy Stage IV Gastric Cancer AJCC v8", "shortest_name_length": 33}
{"curie": "UMLS:C0587219", "names": ["tonsil cyst", "cyst tonsil", "cyst tonsils", "cysts tonsil", "tonsil; cyst", "cyst; tonsil", "cysts tonsils", "Tonsillar cyst", "Tonsillar Cyst", "Cyst of tonsil", "tonsillar cyst", "cyst of tonsil", "cysts tonsillar", "Cyst of tonsil (disorder)", "cyst of tonsil (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cyst of tonsil", "shortest_name_length": 11}
{"curie": "MONDO:0017246", "names": ["congenital extrapulmonary sequestration", "extralobar congenital pulmonary sequestration", "extralobar congenital bronchopulmonary sequestration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extralobar congenital pulmonary sequestration", "shortest_name_length": 39}
{"curie": "MONDO:0005004", "names": ["mesonephroma", "carcinoma cell clear", "carcinoma clear cell", "Clear Cell Carcinoma", "clear cell carcinoma", "Clear cell carcinoma", "carcinomas cell clear", "malignant Mesonephroma", "malignant mesonephroma", "Wolffian duct neoplasm", "Mesonephroma, malignant", "mesonephroma, malignant", "Adenocarcinoma Clear Cell", "Clear cell adenocarcinoma", "clear cell adenocarcinoma", "Clear Cell Adenocarcinoma", "adenocarcinoma cell clear", "Adenocarcinoma, Clear Cell", "Clear Cell Adenocarcinomas", "water-clear cell carcinoma", "Water-clear cell carcinoma", "water-clear cell; carcinoma", "carcinoma; water-clear cell", "Adenocarcinomas, Clear Cell", "Clear cell adenocarcinoma NOS", "Clear cell adenocarcinoma, NOS", "Malignant Glandular Clear Cell", "water-clear cell adenocarcinoma", "Water-clear cell adenocarcinoma", "Water-Clear Cell Adenocarcinoma", "adenocarcinoma; water-clear cell", "water-clear cell; adenocarcinoma", "Mesonephroid Clear cell carcinoma", "Mesonephroid Clear Cell Carcinoma", "mesonephroid clear cell carcinoma", "clear cell adenocarcinoma (diagnosis)", "ADENOCARCINOMA, CLEAR CELL, MALIGNANT", "adenocarcinoma, clear cell, malignant", "Mesonephroid Clear Cell Adenocarcinoma", "Mesonephroid clear cell adenocarcinoma", "mesonephroid clear cell adenocarcinoma", "Clear cell adenocarcinoma, mesonephroid", "mesonephroma NOS (morphologic abnormality)", "Clear cell adenocarcinoma, mesonephroid type", "mesonephroma, malignant (morphologic abnormality)", "clear cell adenocarcinoma (morphologic abnormality)", "Clear cell adenocarcinoma (morphologic abnormality)", "clear cell adenocarcinoma NOS (morphologic abnormality)", "water-clear cell adenocarcinoma (morphologic abnormality)", "Water-clear cell adenocarcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "clear cell adenocarcinoma", "shortest_name_length": 12}
{"curie": "OMIM:607457", "names": ["GIL BLOOD GROUP"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 15}
{"curie": "MONDO:0003585", "names": ["Liposarcoma", "liposarcoma", "Adult Liposarcoma", "adult liposarcoma", "liposarcoma, adult", "sarcoma, lipo-, adult", "liposarcoma of adults"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult liposarcoma", "shortest_name_length": 11}
{"curie": "MONDO:0019214", "names": ["carbohydrate metabolic disorder", "carbohydrate metabolism disorder", "Carbohydrate Metabolism Disorder", "disorder of carbohydrate metabolism", "Carbohydrate Metabolism, Inborn Error", "inborn carbohydrate metabolic disorder", "Carbohydrate Metabolism, Inborn Errors", "inborn carbohydrate metabolism disorder", "inborn errors of carbohydrate metabolism", "inborn carbohydrate metabolic process disorder", "inborn error of carbohydrate metabolic process", "disorder of carbohydrate transport and metabolism", "rare inborn error of carbohydrate metabolic process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn carbohydrate metabolic disorder", "shortest_name_length": 31}
{"curie": "MONDO:0003944", "names": ["endobronchial leiomyoma", "bronchus lung leiomyoma", "Endobronchial Leiomyoma", "lung leiomyoma of bronchus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endobronchial leiomyoma", "shortest_name_length": 23}
{"curie": "MONDO:0045055", "names": ["Glycogen-rich carcinoma", "Glycogen-Rich Carcinoma", "glycogen-rich carcinoma", "[M] Glycogen-rich carcinoma", "Glycogen-rich clear cell carcinoma", "Glycogen-rich carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen-rich carcinoma", "shortest_name_length": 23}
{"curie": "UMLS:C1519925", "names": ["Vaginal Mucinous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Mucinous Adenocarcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0004278", "names": ["Bladder Carcinosarcoma", "sarcomatoid carcinoma of the urinary bladder", "Infiltrating Bladder Urothelial Carcinoma Sarcomatoid Variant", "infiltrating bladder urothelial carcinoma sarcomatoid variant", "Infiltrating Bladder Urothelial Carcinoma, Sarcomatoid Variant", "infiltrating bladder urothelial carcinoma, sarcomatoid variant with heterologous elements", "Infiltrating bladder Urothelial carcinoma, sarcomatoid Variant with Heterologous Elements", "Infiltrating Bladder Urothelial Carcinoma, Sarcomatoid Variant with Heterologous Elements", "Infiltrating bladder Urothelial carcinoma, sarcomatoid Variant without Heterologous Elements", "Infiltrating Bladder Urothelial Carcinoma, Sarcomatoid Variant without Heterologous Elements", "infiltrating bladder urothelial carcinoma, sarcomatoid variant without heterologous elements"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infiltrating bladder urothelial carcinoma sarcomatoid variant", "shortest_name_length": 22}
{"curie": "MONDO:0012292", "names": ["HCV, resistance to", "HCV, RESISTANCE TO", "HCV, susceptibility to", "HCV, SUSCEPTIBILITY TO", "Hepatitis C Virus, resistance to", "HEPATITIS C VIRUS, RESISTANCE TO", "HEPATITIS C VIRUS, SUSCEPTIBILITY TO", "hepatitis C virus, susceptibility to", "hepatitis C virus, response to therapy of", "HEPATITIS C VIRUS INFECTION, RESPONSE TO THERAPY OF", "Hepatitis C Virus infection, response to therapy of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatitis C virus, susceptibility to", "shortest_name_length": 18}
{"curie": "MONDO:0015035", "names": ["Lissencephaly with cerebellar hypoplasia type B", "lissencephaly with cerebellar hypoplasia type B", "Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B", "Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lissencephaly with cerebellar hypoplasia type B", "shortest_name_length": 47}
{"curie": "UMLS:C0520532", "names": ["Subcutaneous hematoma", "hematoma subcutaneous", "subcutaneous hematoma", "SUBCUTANEOUS HEMATOMA", "Subcutaneous haematoma", "SUBCUTANEOUS HAEMATOMA", "Subcutaneous hematoma (disorder)", "subcutaneous hematoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subcutaneous hematoma", "shortest_name_length": 21}
{"curie": "MONDO:0010515", "names": ["MRLS", "Meester-Loeys Syndrome", "MEESTER-LOEYS SYNDROME", "Meester-Loeys syndrome", "Meester-Loeys syndrome; MRLS", "X-linked severe syndromic TAAD", "X-linked severe syndromic thoracic aortic aneurysm and dissection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meester-Loeys syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0035236", "names": ["pustular pyoderma gangrenosum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pustular pyoderma gangrenosum", "shortest_name_length": 29}
{"curie": "MONDO:0007040", "names": ["ACPS3", "ACPS 3", "ACPS III", "Sakati syndrome", "Sakati-Nyhan syndrome", "SAKATI-NYHAN SYNDROME", "ACPS with leg hypoplasia", "ACPS WITH LEG HYPOPLASIA", "ACPS with Leg Hypoplasia", "Sakati-Nyhan-Tisdale syndrome", "Acrocephalopolysyndactyly type 3", "acrocephalopolysyndactyly type 3", "acrocephalopolysyndactyly Type III", "Acrocephalopolysyndactyly Type III", "acrocephalopolysyndactyly type III", "Acrocephalopolysyndactyly type III", "ACROCEPHALOPOLYSYNDACTYLY TYPE III", "Acrocephalopolysyndactyly type III (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sakati-Nyhan syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0004466", "names": ["NEURONITIS", "neuronitis", "Neuronitis", "neuroinflammation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuronitis", "shortest_name_length": 10}
{"curie": "MONDO:0035454", "names": ["BILU syndrome", "Hoffman syndrome", "B-cell immunodeficiency-limb anomaly-urogenital malformation syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-cell immunodeficiency-limb anomaly-urogenital malformation syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0016839", "names": ["distal del(17)(p13.3)", "Distal del(17)(p13.3 )", "distal monosomy 17p13.3", "Distal monosomy 17p13.3", "Distal 17p13.3 microdeletion syndrome", "distal 17p13.3 microdeletion syndrome", "Distal 17p13.3 microdeletion syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal 17p13.3 microdeletion syndrome", "shortest_name_length": 21}
{"curie": "UMLS:C0549310", "names": ["VAGINAL MYCOSIS", "Vaginal mycosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal mycosis", "shortest_name_length": 15}
{"curie": "UMLS:C0333564", "names": ["Blue Body", "Concretion", "Corpora Amylacea", "Corpora amylacea", "CORPORA AMYLACEA", "amylacea; corpora", "corpora; amylacea", "Corpora amylacea (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Corpora amylacea", "shortest_name_length": 9}
{"curie": "MONDO:0016032", "names": ["Short femur", "femur; short", "Short femora", "Short femurs", "short; femur", "Short thighbone", "hypoplasia; femur", "femur; hypoplasia", "Femoral hypoplasia", "congenital short femur", "Congenital short femur", "Hypoplasia of the femora", "short; femur, congenital", "femur; short, congenital", "femoral agenesis/hypoplasia", "Femoral agenesis/hypoplasia", "Femoral intercalary meromelia", "femoral intercalary meromelia", "Congenital hypoplasia of femur", "Congenital hypoplasia of femur (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "femoral agenesis/hypoplasia", "shortest_name_length": 11}
{"curie": "UMLS:C5205871", "names": ["Gastrointestinal Radiation Injury", "GASTROINTESTINAL RADIATION INJURY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal Radiation Injury", "shortest_name_length": 33}
{"curie": "UMLS:C4521799", "names": ["Stage IIB Gastric (Stomach) Cancer", "Clinical Stage IIB Gastric Cancer AJCC v8", "Clinical Stage IIB Gastric Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage IIB Gastric Cancer AJCC v8", "shortest_name_length": 34}
{"curie": "MONDO:0007542", "names": ["CED", "PDD", "DPD1", "CAEND", "Engelmann", "engelmann disease", "ENGELMANN DISEASE", "Engelmann disease", "Engelmann Disease", "Camurati-Engelmann", "engelmann syndrome", "Engelmann syndrome", "Engelman's disease", "Engelmann's disease", "Engelmann's Disease", "engelmann's disease", "diaphyseal dysplasia", "Diaphyseal sclerosis", "Diaphyseal dysplasia", "Engelmann's syndrome", "diaphyseal; dysplasia", "dysplasia; diaphyseal", "Diaphyseal Hyperostoses", "Diaphyseal Hyperostosis", "Hyperostoses, Diaphyseal", "Hyperostosis, Diaphyseal", "camurati-engelmann disease", "Camurati Engelmann Disease", "CAMURATI-ENGELMANN DISEASE", "Camurati-Englemann Disease", "Camurati-Engelmann disease", "Camurati-Engelmann Disease", "Camurati-Englemann disease", "Camurati-Engelmann syndrome", "camurati engelmanns disease", "Camurati Engelmann Syndrome", "Camurati-Engelmann Syndrome", "Diaphyseal dysplasia syndrome", "Diaphyseal dysplasia (disorder)", "Progressive Diaphyseal Dysplasia", "progressive diaphyseal dysplasia", "Progressive diaphyseal dysplasia", "PROGRESSIVE DIAPHYSEAL DYSPLASIA", "Diaphyseal Dysplasia, Progressive", "Dysplasia, Progressive Diaphyseal", "Dysplasias, Progressive Diaphyseal", "Diaphyseal Dysplasias, Progressive", "diaphyseal dysplasia 1, progressive", "DIAPHYSEAL DYSPLASIA 1, PROGRESSIVE", "Diaphyseal Dysplasia 1, Progressive", "progressive diaphyseal dysplasia (diagnosis)", "Osteopathia hyperostotica multiplex infantis", "OSTEOPATHIA HYPEROSTOTICA MULTIPLEX INFANTILIS", "Osteopathia hyperostotica scleroticans multiplex infantis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Camurati-Engelmann disease", "shortest_name_length": 3}
{"curie": "MONDO:0100479", "names": ["RR-TB", "rifampicin-resistant TB", "rifampicin-resistant tuberculosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rifampicin-resistant tuberculosis", "shortest_name_length": 5}
{"curie": "MONDO:0017396", "names": ["toxic dermatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "toxic dermatosis", "shortest_name_length": 16}
{"curie": "MONDO:0013629", "names": ["MRT16", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 16", "mental retardation, autosomal recessive 16", "intellectual disability, autosomal recessive 16", "autosomal recessive intellectual developmental disorder 16", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 16"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 16", "shortest_name_length": 5}
{"curie": "MONDO:0020785", "names": ["CMAVM2", "capillary malformation-arteriovenous malformation 2", "CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "capillary malformation-arteriovenous malformation 2", "shortest_name_length": 6}
{"curie": "MONDO:0014465", "names": ["CILD30", "primary ciliary dyskinesia 30", "CILIARY DYSKINESIA, PRIMARY, 30", "ciliary dyskinesia, primary, 30", "primary ciliary dyskinesia type 30", "CCDC151 primary ciliary dyskinesia", "ciliary dyskinesia, primary, type 30", "primary ciliary dyskinesia 30 without situs inversus", "primary ciliary dyskinesia caused by mutation in CCDC151", "ciliary dyskinesia, primary, 30, with or without situs inversus", "CILIARY DYSKINESIA, PRIMARY, 30, WITH OR WITHOUT SITUS INVERSUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia 30", "shortest_name_length": 6}
{"curie": "MONDO:0025293", "names": ["spiking mortality syndrome", "Spiking Mortality Syndrome", "mortality syndrome, spiking", "Mortality Syndrome, Spiking", "Poult Enteritis Mortality Syndrome", "poult enteritis mortality syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "poult enteritis mortality syndrome", "shortest_name_length": 26}
{"curie": "MONDO:0004931", "names": ["residual stage corticosteroid-induced glaucoma", "Corticosteroid-induced glaucoma, residual stage", "Residual stage of corticosteroid-induced glaucoma", "residual stage of corticosteroid-induced glaucoma", "residual stage corticosteroid-induced open-angle glaucoma", "residual stage of corticosteroid-induced glaucoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "residual stage corticosteroid-induced glaucoma", "shortest_name_length": 46}
{"curie": "MONDO:0007914", "names": ["lumbar stenosis, familial", "Lumbar Stenosis, Familial", "LUMBAR STENOSIS, FAMILIAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lumbar stenosis, familial", "shortest_name_length": 25}
{"curie": "MONDO:0002946", "names": ["Gynatresia", "gynatresia", "Gynatresias"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gynatresia", "shortest_name_length": 10}
{"curie": "UMLS:C4522224", "names": ["Recurrent Anaplastic Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Anaplastic Astrocytoma", "shortest_name_length": 32}
{"curie": "MONDO:0006478", "names": ["UCP", "pancreatic carcinosarcoma", "Pancreatic Carcinosarcoma", "Undifferentiated carcinoma", "Sarcomatoid Pancreatic Carcinoma", "sarcomatoid pancreatic carcinoma", "spindle cell pancreatic carcinoma", "Spindle Cell Pancreatic Carcinoma", "pancreas undifferentiated carcinoma", "Undifferentiated Pancreatic Carcinoma", "undifferentiated pancreatic carcinoma", "Pancreatic Undifferentiated Carcinoma", "undifferentiated carcinoma of pancreas", "Undifferentiated Carcinoma of Pancreas", "Undifferentiated Carcinoma of the Pancreas", "undifferentiated carcinoma of the pancreas", "pleomorphic large cell pancreatic carcinoma", "Pleomorphic Large Cell Pancreatic Carcinoma", "undifferentiated (anaplastic) pancreatic carcinoma", "Undifferentiated (Anaplastic) Pancreatic Carcinoma", "undifferentiated carcinoma of pancreas (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "undifferentiated pancreatic carcinoma", "shortest_name_length": 3}
{"curie": "MONDO:0006949", "names": ["DRUSEN BODY", "drusen retina", "Retinal Drusen", "drusen; bodies", "retinal drusen", "Retinal drusen", "bodies; drusen", "Drusen, Retinal", "Drusen of retina", "Drusen (degenerative)", "Colloid bodies in retina", "Retinal drusen (finding)", "Degenerative drusen of retina", "Drusen (degenerative) of retina"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal drusen", "shortest_name_length": 11}
{"curie": "MONDO:0018643", "names": ["susceptibility to localized juvenile periodontitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "susceptibility to localized juvenile periodontitis", "shortest_name_length": 50}
{"curie": "MONDO:0030339", "names": ["MCPH28", "MICROCEPHALY 28, PRIMARY, AUTOSOMAL RECESSIVE", "microcephaly 28, primary, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly 28, primary, autosomal recessive", "shortest_name_length": 6}
{"curie": "UMLS:C1334061", "names": ["Hyaline Membrane Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyaline Membrane Syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0014145", "names": ["LCA17", "LEBER CONGENITAL AMAUROSIS 17", "Leber congenital amaurosis 17", "GDF6 Leber congenital amaurosis", "Leber congenital amaurosis type 17", "Leber congenital amaurosis caused by mutation in GDF6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leber congenital amaurosis 17", "shortest_name_length": 5}
{"curie": "MONDO:0012166", "names": ["ADSA", "Adsa", "SNAX1", "RNF170 hereditary ataxia", "Ataxia, Sensory, Autosomal Dominant", "ATAXIA, SENSORY, AUTOSOMAL DOMINANT", "autosomal dominant sensory ataxia 1", "ataxia, sensory, 1, autosomal dominant", "ATAXIA, SENSORY, 1, AUTOSOMAL DOMINANT", "hereditary ataxia caused by mutation in RNF170"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant sensory ataxia 1", "shortest_name_length": 4}
{"curie": "UMLS:C3272614", "names": ["Colorectal NET G2", "Colorectal Neuroendocrine Tumor G2", "Large Intestinal Neuroendocrine Tumor G2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Neuroendocrine Tumor G2", "shortest_name_length": 17}
{"curie": "MONDO:0007843", "names": ["KABUK1", "Kabuki syndrome", "Kabuki syndrome 1", "KABUKI syndrome 1", "Kabuki syndrome type 1", "Kabuki make-Up syndrome", "Niikawa-Kuroki syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kabuki syndrome 1", "shortest_name_length": 6}
{"curie": "UMLS:C2216695", "names": ["breast cancer stage I", "Stage I Breast Cancer", "Stage I Breast Cancer AJCC v7", "malignant tumor of breast stage I", "malignant breast neoplasm stage I", "malignant neoplasm of breast stage I", "malignant neoplasm of breast stage I (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant neoplasm of breast stage I", "shortest_name_length": 21}
{"curie": "UMLS:C3641106", "names": ["Congenital Bleeding Defect", "Congenital Bleeding Disorder", "Congenital Coagulation Defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Bleeding Disorder", "shortest_name_length": 26}
{"curie": "MONDO:0011065", "names": ["Hunter-McAlpine syndrome", "Hunter-McAlpine craniosynostosis", "Hunter-McAlpine craniosynostosis syndrome", "HUNTER-MCALPINE CRANIOSYNOSTOSIS SYNDROME", "Hunter McAlpine craniosynostosis syndrome", "Hunter McAlpine craniosynostosis syndrome (disorder)", "craniosynostosis, mental deficiency, almond-shaped palpebral fissures, downturned mouth, mild acral-skeletal anomalies, and short stature"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hunter-McAlpine craniosynostosis", "shortest_name_length": 24}
{"curie": "UMLS:C1334767", "names": ["Minor Salivary Gland Acinic Cell Carcinoma", "Acinic Cell Carcinoma of Minor Salivary Gland", "Minor Salivary Gland Acinic Cell Adenocarcinoma", "Acinic Cell Carcinoma of the Minor Salivary Gland", "Acinic Cell Adenocarcinoma of Minor Salivary Gland", "Acinic Cell Adenocarcinoma of the Minor Salivary Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Minor Salivary Gland Acinic Cell Carcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0002225", "names": ["ovary sarcoma", "Ovarian sarcoma", "ovarian sarcoma", "Ovarian Sarcoma", "Sarcoma of Ovary", "ovarian sarcomas", "sarcoma of Ovary", "Sarcoma of ovary", "sarcoma of ovary", "sarcoma, ovarian", "Sarcoma of the Ovary", "sarcoma of the ovary", "Sarcoma of ovary (disorder)", "sarcoma of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian sarcoma", "shortest_name_length": 13}
{"curie": "MONDO:0001245", "names": ["IRIDA", "IRIDA syndrome", "MICROCYTIC ANEMIA", "anemia microcytic", "ANEMIA MICROCYTIC", "Anemia microcytic", "Microcytic anemia", "Microcytic Anemia", "microcytic anemia", "anemia; microcytic", "Microcytic anaemia", "Anaemia microcytic", "Anaemia;microcytic", "anemias microcytic", "Anemia, microcytic", "microcytic anaemia", "ANAEMIA MICROCYTIC", "Microcytic anemia (disorder)", "Pseudo-Iron-Deficiency Anemia", "PSEUDO-IRON-DEFICIENCY ANEMIA", "Iron-Handling Disorder, Hereditary", "IRON-HANDLING DISORDER, HEREDITARY", "Iron-refractory iron deficiency anemia", "Iron-Refractory Iron Deficiency Anemia", "IRON-REFRACTORY IRON DEFICIENCY ANEMIA", "Iron-refractory iron deficiency anaemia", "IRIDA Iron-refractory iron deficiency anemia", "Iron-refractory iron deficiency anemia (disorder)", "IRIDA (iron-refractory iron deficiency anemia) syndrome", "IRIDA (iron-refractory iron deficiency anaemia) syndrome", "Anemia, Hypochromic Microcytic, with Defect in Iron Metabolism", "ANEMIA, HYPOCHROMIC MICROCYTIC, WITH DEFECT IN IRON METABOLISM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcytic anemia", "shortest_name_length": 5}
{"curie": "UMLS:C1737214", "names": ["Injection site injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site injury", "shortest_name_length": 21}
{"curie": "MONDO:0007734", "names": ["HPE4", "HOLOPROSENCEPHALY 4", "Holoprosencephaly 4", "holoprosencephaly 4", "TGIF1 holoprosencephaly", "Holoprosencephaly Type 4", "holoprosencephaly type 4", "HOLOPROSENCEPHALY 4 (disorder)", "holoprosencephaly caused by mutation in TGIF1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "holoprosencephaly 4", "shortest_name_length": 4}
{"curie": "UMLS:C1167728", "names": ["Viral hemorrhagic cystitis", "Viral haemorrhagic cystitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Viral hemorrhagic cystitis", "shortest_name_length": 26}
{"curie": "UMLS:C3272796", "names": ["Colorectal Sporadic Serrated Polyp"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Sporadic Serrated Polyp", "shortest_name_length": 34}
{"curie": "MONDO:0010911", "names": ["PRLoma", "Prolactinoma", "prolactinoma", "PROLACTINOMA", "Prolactinomas", "prolactinomas", "Lactotroph adenoma", "Lactotrope Adenoma", "lactotroph adenoma", "Lactotroph Adenoma", "lactotrope adenoma", "Adenoma, Lactotroph", "Lactotroph Adenomas", "Adenomas, Lactotroph", "familial prolactinoma", "prolactinoma, familial", "Pituitary prolactinoma", "Pituitary Prolactinoma", "PITUITARY PROLACTINOMA", "pituitary prolactinoma", "Prolactinoma, Familial", "pituitary prolactinomas", "lactotroph cell adenoma", "Prolactinoma (disorder)", "Lactotroph Cell Adenoma", "Lactotroph PitNET/Adenoma", "Prolactinoma of Pituitary", "prolactinoma of pituitary", "prolactin secreting adenoma", "adenoma prolactin secreting", "Prolactin Secreting Adenoma", "Pituitary Gland Prolactinoma", "adenoma, prolactin secreting", "pituitary gland prolactinoma", "Prolactinoma of the Pituitary", "prolactinoma of the pituitary", "Pituitary lactotrophic adenoma", "prolactinoma; unspecified site", "pituitary lactotrophic adenoma", "prolactinoma of pituitary gland", "Prolactinoma of Pituitary Gland", "PRL-secreting pituitary adenoma", "PRL-Secreting Pituitary Adenoma", "PRL Secreting Pituitary Adenoma", "Prolactinoma of Pituitary gland", "PRL-Secreting Pituitary Adenomas", "Pituitary Adenoma, PRL-Secreting", "Pituitary prolactin cell adenoma", "Pituitary Adenomas, PRL-Secreting", "PITUITARY NEOPLASM (PROLACTINOMA)", "Forbes-Albright syndrome (formerly)", "prolactinoma of the pituitary gland", "Prolactinoma of the Pituitary Gland", "prolactin-secreting pituitary adenoma", "Prolactin-secreting pituitary adenoma", "Prolactin-Producing Pituitary Adenoma", "Prolactin-Secreting Pituitary Adenoma", "Prolactin Producing Pituitary Adenoma", "prolactin secreting pituitary adenoma", "Prolactin Secreting Pituitary Adenoma", "PRL producing pituitary gland adenoma", "prolactin producing pituitary adenoma", "PRL Producing Pituitary Gland Adenoma", "Pituitary Adenoma, Prolactin-Secreting", "Prolactin-Producing Pituitary Adenomas", "Pituitary Adenoma, Prolactin Secreting", "PITUITARY ADENOMA, PROLACTIN-SECRETING", "Prolactinoma (morphologic abnormality)", "Prolactin-Secreting Pituitary Adenomas", "Pituitary Adenoma, Prolactin-Producing", "PITUITARY ADENOMA, PROLACTIN SECRETING", "pituitary adenoma, prolactin-secreting", "Adenoma, Prolactin-Secreting, Pituitary", "Pituitary Adenomas, Prolactin-Secreting", "Pituitary Adenomas, Prolactin-Producing", "prolactin producing adenoma of pituitary", "Prolactin Secreting Adenoma of Pituitary", "prolactin secreting adenoma of pituitary", "Prolactin Producing Adenoma of Pituitary", "Lactotroph Pituitary Neuroendocrine Tumor", "Prolactin-Producing Pituitary Gland Tumor", "Prolactin Secreting Pituitary Gland Adenoma", "prolactin producing pituitary gland adenoma", "prolactinoma of pituitary gland (diagnosis)", "prolactin secreting pituitary gland adenoma", "Prolactin-Producing Pituitary Gland Adenoma", "prolactin-producing pituitary gland adenoma", "Prolactin Producing Pituitary Gland Adenoma", "prolactin producing adenoma of the pituitary", "prolactin secreting adenoma of the pituitary", "Prolactin Producing Adenoma of the Pituitary", "Prolactin Secreting Adenoma of the Pituitary", "Prolactin Producing Adenoma of Pituitary Gland", "prolactin secreting adenoma of pituitary gland", "prolactin producing adenoma of pituitary gland", "Prolactin Secreting Adenoma of Pituitary Gland", "Lactotroph Pituitary Neuroendocrine Tumor/Adenoma", "Prolactin Secreting Adenoma of the Pituitary Gland", "Prolactin Producing Adenoma of the Pituitary Gland", "prolactin producing adenoma of the pituitary gland", "prolactin secreting adenoma of the pituitary gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prolactin-producing pituitary gland adenoma", "shortest_name_length": 6}
{"curie": "MONDO:0020113", "names": ["red cell aplasia", "primary acquired red cell aplasia", "primary autoimmune red cell aplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary acquired red cell aplasia", "shortest_name_length": 16}
{"curie": "MONDO:0001126", "names": ["GU", "Ulcer stomach", "gastric ulcer", "Stomach Ulcer", "STOMACH ULCER", "Gastric ulcer", "Ulcer;gastric", "Gastric Ulcer", "Stomach ulcer", "Ulcer;stomach", "ULCER GASTRIC", "Ulcer gastric", "ULCER STOMACH", "GASTRIC ULCER", "stomach ulcer", "Ulcer, Stomach", "stomach; ulcer", "Stomach Ulcers", "gastric ulcers", "Ulcer, Gastric", "Gastric Ulcers", "ulcer; gastric", "stomach ulcers", "Stomach--Ulcers", "Ulcers, Gastric", "Ulcers, Stomach", "ULCUS VENTRICULI", "Ulcus ventriculi", "ulcus ventriculi", "Gastric ulceration", "Stomach ulcer, NOS", "Gastric ulcer, NOS", "GASTRIC ULCERATION", "Stomach Ulceration", "GU - Gastric ulcer", "gastric ulceration", "gastric ulcerations", "Gastric peptic ulcer", "gastric ulcer disease", "GASTRIC ULCER DISEASE", "gastric ulcer (disease)", "Peptic ulcer of stomach", "Gastric ulcer (disorder)", "gastric ulcer (diagnosis)", "Gastric ulcer (diagnosis)", "stomach peptic ulcer disease", "bleeding acute gastric ulcer", "peptic ulcer disease of stomach", "acute gastric ulcer with perforation", "acute gastric ulcer with hemorrhage and perforation", "acute gastric ulcer with hemorrhage and obstruction", "acute gastric ulcer with haemorrhage and perforation", "acute gastric ulcer with perforation and obstruction", "acute gastric ulcer with perforation AND obstruction", "acute gastric ulcer with hemorrhage, with obstruction", "acute gastric ulcer with perforation, with obstruction", "acute gastric ulcer without hemorrhage and without perforation", "chronic gastric ulcer without hemorrhage and without perforation", "chronic gastric ulcer without hemorrhage AND without perforation", "acute gastric ulcer with hemorrhage and perforation, with obstruction", "acute gastric ulcer with hemorrhage, with perforation AND with obstruction", "acute gastric ulcer with hemorrhage, with perforation and with obstruction", "acute gastric ulcer with hemorrhage AND with perforation but without obstruction", "acute gastric ulcer with hemorrhage and with perforation but without obstruction", "acute gastric ulcer without hemorrhage, without perforation AND without obstruction", "acute gastric ulcer without hemorrhage, without perforation and without obstruction", "acute gastric ulcer with hemorrhage and perforation, without mention of obstruction", "chronic gastric ulcer without mention of hemorrhage or perforation, with obstruction", "chronic gastric ulcer without hemorrhage and without perforation but with obstruction", "chronic gastric ulcer without hemorrhage AND without perforation but with obstruction", "acute gastric ulcer without mention of hemorrhage or perforation, without mention of obstruction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric ulcer", "shortest_name_length": 2}
{"curie": "UMLS:C0573229", "names": ["calcium channel blocker overdose", "blockers calcium channel overdose", "overdose of calcium-channel blockers", "Overdose of calcium-channel blockers", "Overdose of calcium-channel blockers (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Overdose of calcium-channel blockers", "shortest_name_length": 32}
{"curie": "MONDO:0009257", "names": ["GALE", "GALE-D", "GALAC3", "Galactosemia 3", "galactosemia 3", "Gale deficiency", "GALE DEFICIENCY", "GALE deficiency", "Galactosemia 3s", "GALE Deficiency", "galactosemia III", "Deficiency, GALE", "GALACTOSEMIA III", "Galactosemia III", "Galactosaemia III", "Galactosemia IIIs", "GALE Deficiencies", "Deficiencies, GALE", "Galactosemia type 3", "galactosemia type 3", "Epimerase deficiency", "Galactoepimerase deficiency", "Galactose Epimerase Deficiency", "galactose epimerase deficiency", "Galactose epimerase deficiency", "GALACTOSE EPIMERASE DEFICIENCY", "Deficiency, Galactose Epimerase", "Galactose Epimerase Deficiencies", "Deficiencies, Galactose Epimerase", "Epimerase deficiency galactosemia", "epimerase deficiency galactosemia", "UDPglucose-4-epimerase deficiency", "Galactosemia - epimerase deficiency", "UDPgalactose-4-epimerase deficiency", "UDP Galactose 4 Epimerase Deficiency", "UDP-GALACTOSE-4-EPIMERASE DEFICIENCY", "UDP-Galactose-4-Epimerase Deficiency", "UDP-galactose-4-epimerase deficiency", "Galactosaemia - epimerase deficiency", "Deficiency, UDP-Galactose-4-Epimerase", "UDP-Galactose-4-Epimerase Deficiencies", "Deficiencies, UDP-Galactose-4-Epimerase", "UDPglucose 4 Epimerase Deficiency Disease", "UDPglucose 4-Epimerase Deficiency Disease", "UDPglucose 4-epimerase deficiency disease", "Deficiency Disease, UDPglucose 4 Epimerase", "Deficiency Disease, UDPglucose 4-Epimerase", "UDP-Galactose-4-Epimerase Deficiency Disease", "UDP Galactose 4 Epimerase Deficiency Disease", "Deficiency Disease, UDP-Galactose-4-Epimerase", "UDP-Galactose-4-Epimerase Deficiency Diseases", "Deficiency Disease, UDP Galactose 4 Epimerase", "Deficiency Diseases, UDP-Galactose-4-Epimerase", "Uridine diphosphate glucose-4-epimerase deficiency", "Uridine diphosphate galactose-4-epimerase deficiency", "uridine diphosphate galactose-4-epimerase deficiency", "Uridine diphosphate galactose-4 epimerase deficiency", "Uridine diphosphate (UDP) glucose-4-epimerase deficiency", "Uridine diphosphate glucose-4-epimerase deficiency (disorder)", "Uridine diphosphate glucose-4-epimerase deficiency (diagnosis)", "galactosemia uridine diphosphate glucose-4-epimerase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "galactose epimerase deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0013389", "names": ["DEE12", "EIEE12", "early infantile epileptic encephalopathy 12", "developmental and epileptic encephalopathy 12", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 12", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 12", "epileptic encephalopathy, early infantile, 12", "PLCB1 early infantile epileptic encephalopathy", "developmental and epileptic encephalopathy, 12", "epileptic encephalopathy, early infantile, type 12", "early infantile epileptic encephalopathy caused by mutation in PLCB1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 12", "shortest_name_length": 5}
{"curie": "MONDO:0001174", "names": ["conjunctival vascular disease", "conjunctival vascular disorder", "Conjunctival Vascular Disorder", "Conjunctival vascular disorder", "conjunctiva; disorder, vascular", "vascular; disorder, conjunctiva", "conjunctival vasculature disease", "conjunctival vascular abnormality", "Conjunctival vascular abnormality", "Conjunctival vascular disorder NOS", "Vascular abnormality of conjunctiva", "disease of conjunctival vasculature", "disorder of conjunctival vasculature", "vascular abnormalities of conjunctiva", "Vascular abnormalities of conjunctiva", "Vascular abnormality of conjunctiva, NOS", "conjunctival vascular disorder (diagnosis)", "conjunctival vasculature disease or disorder", "Vascular abnormality of conjunctiva (disorder)", "disease or disorder of conjunctival vasculature"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "conjunctival vascular disorder", "shortest_name_length": 29}
{"curie": "MONDO:0009347", "names": ["Lipochrome histiocytosis", "Histiocytosis, lipochrome", "familial lipochrome histiocytosis", "Familial lipochrome histiocytosis", "Histiocytosis, Familial Lipochrome", "HISTIOCYTOSIS, FAMILIAL LIPOCHROME", "histiocytosis, familial lipochrome", "Lipochrome histiocytosis - familial", "familial lipochrome histiocytosis (diagnosis)", "Lipochrome histiocytosis - familial (disorder)", "Lipochrome histiocytosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial lipochrome histiocytosis", "shortest_name_length": 24}
{"curie": "MONDO:0017728", "names": ["Tay-Sachs disease, B1 variant", "GM2 gangliosidosis, B1 variant", "hexosaminidase A deficiency, B1 variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tay-Sachs disease, B1 variant", "shortest_name_length": 29}
{"curie": "MONDO:0006619", "names": ["Rash;viral", "rash viral", "Viral rash", "viral rash", "Viral Exanthem", "Viral exanthem", "Viral rash NOS", "VIRAL EXANTHEM", "viral exanthem", "exanthem viral", "exanthems viral", "virus; exanthem", "viral exanthema", "Exanthema;viral", "exanthema; virus", "Viral exanthemata", "viral exanthemata", "Viral exanthema NOS", "Nonspecific viral rash", "nonspecific viral rash", "Non-specific viral rash", "non-specific viral rash", "Viral exanthem (disorder)", "viral exanthem (diagnosis)", "Viral exanthem, unspecified", "Viral exanthema, unspecified", "Other specified viral exanthemata", "Viral disease characterized by exanthem", "Viral disease characterised by exanthem"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "viral exanthem", "shortest_name_length": 10}
{"curie": "MONDO:0024313", "names": ["Staph", "staph infection", "STAPH INFECTION", "staphylococcosis", "Staphylococcosis", "Staphylococcal diseases", "staphylococcal diseases", "Staphylococcal infection", "Staphylococcus infection", "Staphylococcal Infection", "staphylococcal infection", "staphylococcus infection", "Infection staphylococcal", "Infection;staphylococcal", "Staphylococcal Infections", "staphylococcal infections", "staphylococcal; infection", "STAPHYLOCOCCAL INFECTIONS", "Staphylococcal infections", "infection; staphylococcal", "Infections, Staphylococcal", "Staphylococcal infection NOS", "Staphylococcal infection, NOS", "staphylococcal skin infections", "staphylococcus bacteria infection", "Staphylococcal infectious disease", "staphylococcal infection (diagnosis)", "Staphylococcal infection, unspecified", "Staphylococcal infectious disease, NOS", "Staphylococcal infectious disease (disorder)", "Bacterial infection due to unspecified staphylococcus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "staphylococcal infection", "shortest_name_length": 5}
{"curie": "MONDO:0024770", "names": ["DEX", "AIFBL2", "DEFICIENCY IN ELF4, X-LINKED", "deficiency 1n ELF4, X-linked", "AUTOINFLAMMATORY SYNDROME, FAMILIAL, X-LINKED, BEHCET-LIKE 2", "autoinflammatory syndrome, familial, X-linked, Behcet-like 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoinflammatory syndrome, familial, X-linked, Behcet-like 2", "shortest_name_length": 3}
{"curie": "MONDO:0001035", "names": ["Hypopyon ulcer", "hypopyon ulcer", "ulcer; hypopyon", "hypopyon; ulcer", "hypopyon corneal ulcer", "Hypopyon ulcer (disorder)", "Corneal ulcer with hypopyon", "hypopyon corneal ulcer (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypopyon ulcer", "shortest_name_length": 14}
{"curie": "MONDO:0100281", "names": ["WM1", "macroglobulinemia, Waldenstrom, 1", "macroglobulinemia, Waldenstrom, somatic", "macroglobulinemia, waldenstrom, susceptibility to, 1", "MACROGLOBULINEMIA, WALDENSTROM, SUSCEPTIBILITY TO, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macroglobulinemia, Waldenstrom, 1", "shortest_name_length": 3}
{"curie": "UMLS:C3898127", "names": ["Soft Tissue Sarcoma", "Localized Childhood Soft Tissue Sarcoma", "Non-Metastatic Childhood Soft Tissue Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Metastatic Childhood Soft Tissue Sarcoma", "shortest_name_length": 19}
{"curie": "MONDO:0010492", "names": ["PAGH2", "PITA2", "X-linked acromegaly", "acromegaly, X-linked", "ACROMEGALY, X-LINKED", "GPR101 pituitary gland adenoma", "GH-secreting pituitary adenoma 2", "pituitary adenoma 2, GH-secreting", "ACROMEGALY DUE TO PITUITARY ADENOMA 2", "acromegaly due to pituitary adenoma 2", "growth hormone secreting pituitary adenoma 2", "PITUITARY ADENOMA 2, GROWTH HORMONE-SECRETING", "pituitary adenoma 2, growth hormone-secreting", "pituitary adenoma 2, Growth hormone-secreting", "pituitary adenoma, growth hormone-secreting, 2", "pituitary adenoma, Growth hormone-secreting, type 2", "pituitary gland adenoma caused by mutation in GPR101"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pituitary adenoma, growth hormone-secreting, 2", "shortest_name_length": 5}
{"curie": "UMLS:C2981411", "names": ["Stage II Gastric Gastrointestinal Stromal Tumor", "Stage II Gastric Gastrointestinal Stromal Tumor AJCC v7", "Stage II Gastric (Stomach) Gastrointestinal Stromal Tumor (GIST)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Gastric Gastrointestinal Stromal Tumor", "shortest_name_length": 47}
{"curie": "UMLS:C4552931", "names": ["II", "Stage II Bladder Cancer", "Stage II Bladder Cancer AJCC v8", "Stage II Bladder Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Bladder Cancer AJCC v8", "shortest_name_length": 2}
{"curie": "UMLS:C2984108", "names": ["Nasopharyngeal Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasopharyngeal Carcinoma by AJCC v7 Stage", "shortest_name_length": 41}
{"curie": "UMLS:C4054163", "names": ["Posterior Urethral Valves Type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Posterior Urethral Valves Type 1", "shortest_name_length": 32}
{"curie": "UMLS:C4525744", "names": ["Colon Neuroendocrine Tumor by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colon Neuroendocrine Tumor by AJCC v8 Stage", "shortest_name_length": 43}
{"curie": "MONDO:0019911", "names": ["UPD(4)mat", "maternal uniparental disomy chromosome 4", "Maternal uniparental disomy of chromosome 4", "maternal uniparental disomy of chromosome 4", "maternal uniparental disomy of chromosome type 4", "Maternal uniparental disomy of chromosome 4 (disorder)", "Maternal uniparental disomy of chromosome 4 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maternal uniparental disomy of chromosome 4", "shortest_name_length": 9}
{"curie": "MONDO:0013796", "names": ["Dup(17)(q12)", "dup(17)(q12)", "Trisomy 17q12", "trisomy 17q12", "17q12 duplication", "17q12 microduplication", "17q12 duplication syndrome", "recurrent duplication of 17q12", "17q12 microduplication syndrome", "CHROMOSOME 17q12 DUPLICATION SYNDROME", "Chromosome 17q12 duplication syndrome", "chromosome 17q12 duplication syndrome", "17q12 microduplication syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 17q12 duplication syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0007019", "names": ["VULVOVAGINITIS", "Vulvovaginitis", "vulvovaginitis", "Vulvo-vaginitis", "Vulvovaginitides", "Vulvovaginitis NOS", "Vulvovaginitis, NOS", "Vulvovaginitis (disorder)", "vulvovaginitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvovaginitis", "shortest_name_length": 14}
{"curie": "MONDO:0003321", "names": ["WT1", "Familiar Wilms Tumor", "familial Wilms tumor", "Wilms tumor, familial", "familial Wilms' tumor", "Familial Wilms' Tumor", "hereditary Wilms tumor", "Hereditary Wilms Tumor", "Hereditary Wilms tumor", "Hereditary Wilms tumour", "Hereditary Wilms' Tumor", "hereditary Wilms' tumor", "hereditary Wilms' tumour", "hereditary nephroblastoma", "Familial Kidney Wilms Tumor", "hereditary renal adenosarcoma", "Hereditary Kidney Wilms Tumor", "Hereditary Renal Adenosarcoma", "hereditary Wilms' tumor (WT1)", "Hereditary Kidney Adenosarcoma", "hereditary kidney adenosarcoma", "Hereditary Nephroblastoma (WT1)", "Hereditary Kidney Nephroblastoma", "Hereditary Renal Adenosarcoma (WT1)", "Hereditary Kidney Adenosarcoma (WT1)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary Wilms tumor", "shortest_name_length": 3}
{"curie": "UMLS:C4329967", "names": ["Factor V Inactivation", "Factor V Inhibitor Present"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Factor V Inactivation", "shortest_name_length": 21}
{"curie": "UMLS:C1332486", "names": ["Benign Pediatric Supratentorial Tumor", "Benign Childhood Supratentorial Tumor", "Childhood Benign Supratentorial Tumors", "Benign Pediatric Supratentorial Neoplasm", "Benign Childhood Supratentorial Neoplasm", "Childhood Benign Supratentorial Neoplasms"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Childhood Supratentorial Neoplasm", "shortest_name_length": 37}
{"curie": "UMLS:C4521800", "names": ["Stage 0 Anal Cancer", "Stage 0 Anal Cancer AJCC v8", "Stage 0 Anal Carcinoma AJCC v8", "Stage 0 Anal Canal and Perianal (Anal Margin) Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Anal Cancer AJCC v8", "shortest_name_length": 19}
{"curie": "UMLS:C4528743", "names": ["Refractory High Risk Myelodysplastic Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory High Risk Myelodysplastic Syndrome", "shortest_name_length": 45}
{"curie": "UMLS:C0279737", "names": ["low-grade salivary gland cancer", "Low Grade Salivary Gland Cancer", "salivary gland cancer, low grade", "Low Grade Salivary Gland Carcinoma", "low-grade salivary gland carcinoma", "salivary gland carcinoma, low grade", "Low-Grade Carcinoma of Salivary Gland", "cancer of the salivary gland, low grade", "Low-Grade Carcinoma of the Salivary Gland", "carcinoma of the salivary gland, low grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Grade Salivary Gland Carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0000415", "names": ["adolescence-adult electroclinical syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adolescence-adult electroclinical syndrome", "shortest_name_length": 42}
{"curie": "UMLS:C2217809", "names": ["stage IVA vulvar cancer", "Stage IVA Vulvar Cancer", "vulvar cancer stage IVa", "Stage IVA Vulvar Carcinoma", "stage IVA vulvar carcinoma", "stage IVA vulvar cancer AJCC v7", "Stage IVA Vulvar Cancer AJCC v7", "malignant tumor of vulva stage IVa", "Stage IVA Vulvar Carcinoma AJCC v7", "stage IVA vulvar carcinoma AJCC v7", "malignant neoplasm of vulva stage IVa", "malignant neoplasm of vulva stage IVa (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Vulvar Cancer AJCC v7", "shortest_name_length": 23}
{"curie": "MONDO:0044660", "names": ["luteal-phase-dependent periodic fever", "Luteal-phase-dependent periodic fever", "Luteal phase dependent periodic fever", "Luteal-phase-dependent febrile episode", "Periodic fever, luteal phase-dependent", "luteal-phase-dependent febrile episode", "Luteal phase dependent febrile episode", "Menstrual cycle-dependent periodic fever", "Menstrual cycle dependent periodic fever", "menstrual cycle-dependent periodic fever", "periodic fever, menstrual cycle-dependent", "periodic fever, menstrual cycle dependent", "PERIODIC FEVER, MENSTRUAL CYCLE-DEPENDENT", "Menstrual cycle dependent febrile episode", "Menstrual cycle-dependent febrile episode", "menstrual cycle-dependent febrile episode", "Menstrual cycle dependent periodic fever (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "menstrual cycle-dependent periodic fever", "shortest_name_length": 37}
{"curie": "UMLS:C0149732", "names": ["myorrhexis", "Myorrhexis", "muscle tear", "Tear;muscle", "Muscle tear", "Torn muscle", "torn muscle", "Muscle tears", "muscles tear", "muscle tears", "muscles tears", "muscle rupture", "MUSCLE RUPTURE", "muscle tearing", "Muscle rupture", "muscle ruptures", "muscles ruptures", "Rupture of muscle", "rupture of muscle", "Rupture of muscle (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rupture of muscle", "shortest_name_length": 10}
{"curie": "UMLS:C3899192", "names": ["Extended Oligoarticular JIA", "Extended Oligoarticular Juvenile Idiopathic Arthritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extended Oligoarticular Juvenile Idiopathic Arthritis", "shortest_name_length": 27}
{"curie": "UMLS:C0151698", "names": ["INJECTION SITE BLEEDING", "Injection site bleeding", "Hemorrhage injection site", "INJECTION SITE HEMORRHAGE", "HEMORRHAGE INJECTION SITE", "Injection site hemorrhage", "Injection site haemorrhage", "Haemorrhage injection site", "Injection site bleeding spot", "Injection site hemorrhage (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site hemorrhage", "shortest_name_length": 23}
{"curie": "UMLS:C0266336", "names": ["Acystia", "acystia", "atresia; bladder", "Bladder agenesis", "bladder; atresia", "bladder agenesis", "absence; bladder", "bladder; agenesis", "agenesis; bladder", "Absence of bladder", "Agenesis of bladder", "Absence of the bladder", "bladder; absence, congenital", "absence; bladder, congenital", "congenital absence of bladder", "Congenital absence of bladder", "Agenesis of bladder (disorder)", "Congenital absence of bladder (disorder)", "congenital absence of bladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Agenesis of bladder", "shortest_name_length": 7}
{"curie": "MONDO:0032909", "names": ["MC3DN10", "mitochondrial complex 3 deficiency, nuclear type 10", "MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 3 deficiency, nuclear type 10", "shortest_name_length": 7}
{"curie": "UMLS:C1611713", "names": ["hyperperfusion syndrome", "Cerebral Hyperperfusion Syndrome", "cerebral hyperperfusion syndrome", "Cerebral hyperperfusion syndrome", "cerebral hyperperfusion syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebral hyperperfusion syndrome", "shortest_name_length": 23}
{"curie": "UMLS:C0039437", "names": ["teething", "Teething", "teeth syndrome", "Teething syndrome", "TEETHING SYNDROME", "Teething Syndrome", "teething syndrome", "Teething syndrome (finding)", "teething syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Teething syndrome", "shortest_name_length": 8}
{"curie": "MONDO:0032582", "names": ["NPHS19", "nephrotic syndrome type 19", "NEPHROTIC SYNDROME, TYPE 19", "nephrotic syndrome, type 19"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrotic syndrome, type 19", "shortest_name_length": 6}
{"curie": "MONDO:0003818", "names": ["childhood mature ovarian teratoma", "pediatric ovarian mature teratoma", "childhood ovarian mature teratoma", "Childhood Ovarian Mature Teratoma", "Pediatric Ovarian Mature Teratoma", "pediatric mature ovarian teratoma", "Pediatric Mature Teratoma of Ovary", "childhood mature teratoma of ovary", "pediatric mature teratoma of ovary", "Childhood Mature Teratoma of Ovary", "pediatric Mature teratoma of Ovary", "mature ovarian teratoma of childhood", "pediatric mature teratoma of the ovary", "childhood mature teratoma of the ovary", "Pediatric Mature Teratoma of the Ovary", "Childhood Mature Teratoma of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood mature teratoma of the ovary", "shortest_name_length": 33}
{"curie": "UMLS:C4524797", "names": ["Gastric Cancer by AJCC v8 cTNM Stage", "Gastric Cancer by AJCC v8 Clinical Stage", "Gastric Carcinoma by AJCC v8 Clinical Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Cancer by AJCC v8 Clinical Stage", "shortest_name_length": 36}
{"curie": "UMLS:C0855111", "names": ["Relapsed Diffuse Large B-Cell Lymphoma", "Diffuse large B-cell lymphoma recurrent", "Recurrent Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse large B-cell lymphoma recurrent", "shortest_name_length": 38}
{"curie": "MONDO:0002257", "names": ["Ankyloses", "ankyloses", "Ankylosis", "ANKYLOSIS", "ANKYLOSES", "ankylosis", "Joint fused", "Frozen joint", "frozen joint", "joint fusion", "Joint fusion", "joint; fusion", "fusion; joint", "frozen joints", "Ankylosis, NOS", "Fusion of joint", "fusion of joint", "Joint ankylosis", "joint ankylosis", "Joint Ankylosis", "Ankylosed joints", "ankylosis was seen", "Ankylosis of joint", "ankylosis of joint", "ankylosis (disease)", "Fusion of joint, NOS", "Ankylosis of joint (disorder)", "ankylosis of joint (diagnosis)", "Ankylosis (morphologic abnormality)", "Ankylosis of joint, site unspecified", "ankylosis of joint (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ankylosis", "shortest_name_length": 9}
{"curie": "MONDO:0004004", "names": ["NEURITIS MOTOR", "Motor neuritis", "motor neuritis", "Motor Neuritis", "Neuritis motor", "Neuritis, Motor", "Motor Neuritides", "motor neuropathy", "Motor neuropathy", "Neuritides, Motor", "motor nerve neuritis", "motor peripheral neuropathy", "Motor peripheral neuropathy", "PERIPHERAL MOTOR NEUROPATHY", "Peripheral motor neuropathy", "peripheral motor neuropathy", "Peripheral Motor Neuropathy", "peripheral neuropathy motor", "Peripheral motor neuropathy (disorder)", "Peripheral motor neuropathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "motor nerve neuritis", "shortest_name_length": 14}
{"curie": "UMLS:C1368669", "names": ["Benign Adrenal Cortex Tumor", "Benign adrenal cortical tumor", "Benign adrenal cortical tumour", "Benign Adrenal Cortex Neoplasm", "Benign tumor of adrenal cortex", "Adrenal cortical tumor, benign", "Benign tumour of adrenal cortex", "Adrenal cortical tumour, benign", "Benign Adrenal Cortical Neoplasm", "benign neoplasm of adrenal cortex", "Benign neoplasm of adrenal cortex", "Benign neoplasm of adrenal cortex (disorder)", "benign neoplasm of adrenal cortex (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign neoplasm of adrenal cortex", "shortest_name_length": 27}
{"curie": "MONDO:0018108", "names": ["idiopathic disseminated CMV infection", "idiopathic disseminated cytomegalovirus infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic disseminated cytomegalovirus infection", "shortest_name_length": 37}
{"curie": "UMLS:C0280952", "names": ["drug extravasation", "Drug Extravasation", "extravasation, drug", "Extravasation of drug", "Extravasation of drug (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extravasation of drug", "shortest_name_length": 18}
{"curie": "MONDO:0030985", "names": ["POI19", "POF19", "PREMATURE OVARIAN FAILURE 19", "premature ovarian failure 19", "primary ovarian insufficiency 19"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "premature ovarian failure 19", "shortest_name_length": 5}
{"curie": "MONDO:0007234", "names": ["Branchial Myoclonus with Spastic Paraparesis and Cerebellar Ataxia", "branchial myoclonus with spastic paraparesis and cerebellar ataxia", "BRANCHIAL MYOCLONUS WITH SPASTIC PARAPARESIS AND CEREBELLAR ATAXIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "branchial myoclonus with spastic paraparesis and cerebellar ataxia", "shortest_name_length": 66}
{"curie": "MONDO:0014079", "names": ["RLS8", "restless legs syndrome 8", "RESTLESS LEGS SYNDROME, SUSCEPTIBILITY TO, 8", "restless legs syndrome, susceptibility to, 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "restless legs syndrome, susceptibility to, 8", "shortest_name_length": 4}
{"curie": "MONDO:0006005", "names": ["VEE", "Venezuelan equine fever", "Venezuelan Equine Fever", "fever; Venezuelan equine", "Venezuelan equine; fever", "Venezuelan Equine Encephalitis", "Encephalitis venezuelan equine", "Venezuelan equine encephalitis", "venezuelan equine encephalitis", "Encephalitis, Venezuelan Equine", "Equine Encephalitis, Venezuelan", "Venezuelan equine encephalomyelitis", "Venezuelan Equine Encephalomyelitis", "VEE - Venezuelan equine encephalitis", "Equine Encephalomyelitis, Venezuelan", "Encephalomyelitis, Venezuelan Equine", "Equine encephalitis, Venezuelan (VEE)", "Venezuelan Equine Encephalomyelitides", "Equine Encephalomyelitides, Venezuelan", "Encephalomyelitides, Venezuelan Equine", "Venezuelan equine encephalitis (diagnosis)", "Venezuelan equine encephalitis virus infection", "Disorder due to Venezuelan equine encephalitis virus", "Venezuelan equine encephalitis virus infectious disease", "Disorder caused by Venezuelan equine encephalitis virus", "Venezuelan equine encephalitis virus disease or disorder", "Venezuelan equine encephalitis virus non-neuroinvasive disease", "Venezuelan equine encephalitis virus caused disease or disorder", "Disorder caused by Venezuelan equine encephalitis virus (disorder)", "Venezuelan equine encephalitis virus non-neuroinvasive disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Venezuelan equine encephalitis", "shortest_name_length": 3}
{"curie": "MONDO:0015082", "names": ["IPP-Gelfand syndrome", "alopecia antibody deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alopecia antibody deficiency", "shortest_name_length": 20}
{"curie": "UMLS:C3146252", "names": ["Stage II Colorectal Cancer", "Stage II Colorectal Cancer AJCC v7", "Stage II Colorectal (Colon or Rectal) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Colorectal Cancer AJCC v7", "shortest_name_length": 26}
{"curie": "MONDO:0016734", "names": ["AGNG", "Anaplastic Ganglioglioma", "anaplastic ganglioglioma", "Anaplastic ganglioglioma", "Ganglioglioma, anaplastic", "Anaplastic ganglioglioma (disorder)", "anaplastic ganglioglioma (diagnosis)", "Ganglioglioma, anaplastic (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anaplastic ganglioglioma", "shortest_name_length": 4}
{"curie": "MONDO:0013895", "names": ["AOS3", "ADAMS-OLIVER SYNDROME 3", "Adams-Oliver syndrome 3", "RBPJ Adams-Oliver syndrome", "Adams-Oliver syndrome type 3", "Adams-Oliver syndrome caused by mutation in RBPJ"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adams-Oliver syndrome 3", "shortest_name_length": 4}
{"curie": "UMLS:C0279958", "names": ["Stage I Diffuse Small Cleaved Cell Lymphoma", "stage I adult diffuse small cleaved cell lymphoma", "Stage I Adult Diffuse Small Cleaved Cell Lymphoma", "Adult Diffuse Small Cleaved Cell Lymphoma Stage I", "adult diffuse small cleaved cell lymphoma, stage I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Adult Diffuse Small Cleaved Cell Lymphoma", "shortest_name_length": 43}
{"curie": "UMLS:C0403677", "names": ["bladder injury", "injury bladder", "BLADDER INJURY", "Bladder injury", "Bladder Injury", "bladder; injury", "injury; bladder", "bladder injuries", "Injury of bladder", "Bladder injury NOS", "Injury of bladder, NOS", "bladder injury (diagnosis)", "Injury of bladder (disorder)", "Unspecified injury of bladder", "Injury of bladder, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of bladder", "shortest_name_length": 14}
{"curie": "MONDO:0013020", "names": ["NRCLP5", "narcolepsy 5", "NARCOLEPSY 5, SUSCEPTIBILITY TO", "narcolepsy 5, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "narcolepsy 5, susceptibility to", "shortest_name_length": 6}
{"curie": "MONDO:0006700", "names": ["Choroid Tumor", "choroid cancer", "choroidal tumor", "Choroidal tumor", "Choroidal Tumor", "Tumor of choroid", "Choroid Neoplasm", "choroid neoplasm", "Tumor of Choroid", "neoplasm choroid", "Choroid neoplasm", "Neoplasm, Choroid", "Tumour of choroid", "Choroid Neoplasms", "Neoplasms, Choroid", "Choroidal Neoplasm", "Choroidal Neoplasms", "Neoplasm of choroid", "neoplasm of choroid", "Neoplasm of Choroid", "Neoplasm, Choroidal", "eye neoplasm choroid", "optic choroid cancer", "Neoplasms, Choroidal", "Tumor of the Choroid", "Malignant Choroid Tumor", "malignant choroid tumor", "cancer of optic choroid", "Neoplasm of the Choroid", "malignant tumor of choroid", "malignant choroid neoplasm", "Malignant Choroid Neoplasm", "Malignant tumor of choroid", "Malignant Tumor of Choroid", "Malignant tumour of choroid", "Malignant neoplasm of choroid", "Malignant Neoplasm of Choroid", "malignant neoplasm of choroid", "malignant tumor of the Choroid", "Neoplasm of choroid (disorder)", "malignant tumor of the choroid", "Malignant Tumor of the Choroid", "Neoplasm of choroid (diagnosis)", "malignant optic choroid neoplasm", "malignant neoplasm of the choroid", "Malignant Neoplasm of the Choroid", "malignant neoplasm of optic choroid", "malignant neoplasm of choroid of eye", "Malignant tumor of choroid (disorder)", "malignant neoplasm of choroid of eye (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choroid cancer", "shortest_name_length": 13}
{"curie": "UMLS:C5206569", "names": ["Refractory High Risk Acute Myeloid Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory High Risk Acute Myeloid Leukemia", "shortest_name_length": 43}
{"curie": "MONDO:0018690", "names": ["Adie", "adie pupil", "Adie Pupil", "ADIE PUPIL", "PUPIL ADIE", "Adie pupil", "Tonic Pupil", "tonic pupil", "Adies Pupil", "Tonic pupil", "adies pupil", "Pupil, Adie", "Pupil, Tonic", "Adie's Pupil", "Tonic Pupils", "adies pupils", "Adie's pupil", "tonic pupils", "adie's pupil", "Pupil Adie's", "Pupillotonia", "pupillotonia", "Pupils, Tonic", "adie syndrome", "ADIE SYNDROME", "Adie syndrome", "Adie Syndrome", "Pupillotonias", "Pupil, Adie's", "Pupils, Adie's", "Myotonic pupil", "Myotonic Pupil", "Syndrome, Adie", "Pupil, Myotonic", "Adie's syndrome", "Adie's Syndrome", "adie's syndrome", "Myotonic Pupils", "Syndrome, Adie's", "Pupils, Myotonic", "Holmes-Adie pupil", "Adie's tonic pupil", "HOLMES-ADIE SYNDROME", "Holmes-Adie syndrome", "Holmes Adie Syndrome", "Holmes-Adie Syndrome", "adie holmes syndrome", "holmes adie syndrome", "holmes-adie syndrome", "Poorly Reacting Pupil", "Syndrome, Holmes-Adie", "Adie's pupil syndrome", "POORLY REACTING PUPILS", "Pupil, Poorly Reacting", "Poorly Reacting Pupils", "poorly Reacting pupils", "Pupils, Poorly Reacting", "Tonic pupillary reaction", "Adie's pupil or syndrome", "Adie's tonic pupil (diagnosis)", "Adie's pupil (physical finding)", "Tonic pupillary reaction (disorder)", "Tonic pupil-tendon areflexia syndrome", "tonic pupil-tendon areflexia syndrome", "accommodation Adie's pupil (large, slowly reactive)", "the pupils reacted sluggishly but completely to light", "tonic, sluggishly reacting pupil and hypoactive or absent tendon reflexes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Holmes-Adie syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0045058", "names": ["ACTH producing pituitary tumor", "ACTH-producing pituitary tumor", "ACTH-producing pituitary tumour", "pituitary tumor, ACTH-producing", "ACTH-secreting tumor of pituitary", "ACTH-producing pituitary neoplasm", "ACTH-Producing Pituitary Gland Tumor", "ACTH-secreting tumor of the pituitary", "ACTH producing pituitary gland neoplasm", "pituitary corticotropin secreting tumor", "ACTH-Producing Pituitary Gland Neoplasm", "ACTH-producing pituitary gland neoplasm", "pituitary corticotropin secreting neoplasm", "adrenocorticotropin secreting tumor of pituitary", "corticotropin secreting pituitary gland neoplasm", "adrenocorticotropin secreting neoplasm of pituitary", "adrenocorticotropin secreting pituitary gland tumor", "adrenocorticotropin producing pituitary gland tumor", "adrenocorticotropin secreting tumor of the pituitary", "adrenocorticotropin secreting neoplasm of the pituitary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ACTH-producing pituitary gland neoplasm", "shortest_name_length": 30}
{"curie": "MONDO:0019712", "names": ["patellar dysostosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "patellar dysostosis", "shortest_name_length": 19}
{"curie": "UMLS:C4684863", "names": ["Refractory Peripheral Primitive Neuroectodermal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Peripheral Primitive Neuroectodermal Tumor", "shortest_name_length": 53}
{"curie": "UMLS:C1333836", "names": ["Grade 2 Cutaneous Follicular Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade 2 Cutaneous Follicular Lymphoma", "shortest_name_length": 37}
{"curie": "MONDO:0019412", "names": ["Dysspondyloenchondromatosis", "dysspondyloenchondromatosis", "Dysspondyloenchondromatosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dysspondyloenchondromatosis", "shortest_name_length": 27}
{"curie": "MONDO:0006068", "names": ["ACTHoma", "Corticotropinoma", "corticotroph adenoma", "Corticotropic Adenoma", "corticotropic adenoma", "Corticotroph PitNET/Adenoma", "Pituitary ACTH Secreting Adenoma", "Pituitary ACTH-Secreting Adenoma", "pituitary ACTH secreting adenoma", "ACTH-Producing Pituitary Adenoma", "pituitary ACTH-secreting adenoma", "ACTH-producing pituitary adenoma", "ACTH secreting adenoma of pituitary", "ACTH-secreting adenoma of pituitary", "ACTH Secreting Adenoma of Pituitary", "ACTH Producing Pituitary Gland Adenoma", "pituitary gland ACTH-secreting adenoma", "ACTH-Producing Pituitary Gland Adenoma", "Pituitary Gland ACTH-Secreting Adenoma", "ACTH-producing pituitary gland adenoma", "ACTH producing pituitary gland adenoma", "ACTH secreting adenoma of the pituitary", "ACTH-secreting adenoma of the pituitary", "ACTH Secreting Adenoma of the Pituitary", "pituitary corticotropin secreting adenoma", "Pituitary Corticotropin Secreting Adenoma", "ACTH-secreting adenoma of pituitary gland", "Corticotroph Pituitary Neuroendocrine Tumor", "ACTH-secreting adenoma of the pituitary gland", "Corticotropin Secreting Pituitary Gland Adenoma", "Adrenocorticotropin Producing Pituitary Adenoma", "Adrenocorticotropin Secreting Pituitary Adenoma", "corticotropin secreting pituitary gland adenoma", "adrenocorticotropin producing pituitary adenoma", "adrenocorticotropin secreting pituitary adenoma", "corticotropin secreting adenoma of the pituitary", "Corticotropin Secreting Adenoma of the Pituitary", "Adrenocorticotropin Producing Adenoma of Pituitary", "adrenocorticotropin producing adenoma of pituitary", "Adrenocorticotropin Secreting Adenoma of Pituitary", "adrenocorticotropin secreting adenoma of pituitary", "Corticotroph Pituitary Neuroendocrine Tumor/Adenoma", "Adrenocorticotropin Producing Pituitary Gland Adenoma", "adrenocorticotropin secreting pituitary gland adenoma", "Adrenocorticotropin Secreting Pituitary Gland Adenoma", "adrenocorticotropin producing pituitary gland adenoma", "Adrenocorticotropin Secreting Adenoma of the Pituitary", "adrenocorticotropin secreting adenoma of the pituitary", "Adrenocorticotropin Producing Adenoma of the Pituitary", "adrenocorticotropin producing adenoma of the pituitary", "adrenocorticotropin producing adenoma of pituitary gland", "Adrenocorticotropin Secreting Adenoma of Pituitary Gland", "adrenocorticotropin secreting adenoma of pituitary gland", "Adrenocorticotropin Producing Adenoma of Pituitary Gland", "adrenocorticotropin secreting adenoma of the pituitary gland", "Adrenocorticotropin Secreting Adenoma of the Pituitary Gland", "adrenocorticotropin producing adenoma of the pituitary gland", "Adrenocorticotropin Producing Adenoma of the Pituitary Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ACTH-producing pituitary gland adenoma", "shortest_name_length": 7}
{"curie": "UMLS:C0269164", "names": ["rupture ovary", "ovary rupture", "ovary; rupture", "rupture; ovary", "Ovarian rupture", "ovarian rupture", "Ovarian Rupture", "rupture of ovary", "Rupture of ovary", "Rupture of ovary (disorder)", "rupture of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Rupture", "shortest_name_length": 13}
{"curie": "UMLS:C1332363", "names": ["B-Cell Proliferation of Uncertain Malignant Potential"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-Cell Proliferation of Uncertain Malignant Potential", "shortest_name_length": 53}
{"curie": "UMLS:C2700125", "names": ["Urinary Tract Stenosis", "Urinary Tract Stricture"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urinary Tract Stenosis", "shortest_name_length": 22}
{"curie": "UMLS:C1388177", "names": ["Aortic plaque", "Complex aortic plaque", "aortic arteriosclerosis", "Aortic arteriosclerosis", "Aortic Arteriosclerosis", "arteriosclerosis; aorta", "aorta; arteriosclerosis", "Arteriosclerosis of aorta", "arteriosclerosis of aorta", "Arteriosclerosis of aorta (disorder)", "arteriosclerosis of aorta (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arteriosclerosis of aorta", "shortest_name_length": 13}
{"curie": "MONDO:0008035", "names": ["muscular hypoplasia, congenital universal, of Krabbe", "MUSCULAR HYPOPLASIA, CONGENITAL UNIVERSAL, OF KRABBE", "Muscular Hypoplasia, Congenital Universal, of Krabbe"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular hypoplasia, congenital universal, of Krabbe", "shortest_name_length": 52}
{"curie": "MONDO:0021123", "names": ["Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor of Bone", "Ewing sarcoma/peripheral primitive neuroectodermal tumor of bone", "Ewing's Sarcoma/Peripheral Primitive Neuroectodermal Tumor of Bone", "Ewing's sarcoma/peripheral primitive neuroectodermal tumor of bone", "bone tissue Ewing sarcoma/peripheral primitive neuroectodermal tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ewing sarcoma/peripheral primitive neuroectodermal tumor of bone", "shortest_name_length": 64}
{"curie": "UMLS:C1333401", "names": ["ECL Cell NET G1", "Enterochromaffin-Like Cell NET G1", "Enterochromaffin-Like Cell Carcinoid Tumor", "Enterochromaffin-Like Cell Neuroendocrine Tumor", "Enterochromaffin-Like Cell Neuroendocrine Tumor G1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Enterochromaffin-Like Cell Neuroendocrine Tumor G1", "shortest_name_length": 15}
{"curie": "UMLS:C4525300", "names": ["Gallbladder cancer", "Stage IIA Gallbladder Cancer", "stage IIA gallbladder cancer", "Stage IIA Gallbladder Cancer AJCC v8", "stage IIA gallbladder cancer AJCC v8", "stage IIA gallbladder carcinoma AJCC v8", "Stage IIA Gallbladder Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Gallbladder Cancer AJCC v8", "shortest_name_length": 18}
{"curie": "MONDO:0006690", "names": ["Thrombosis carotid", "Carotid thrombosis", "Carotid Thrombosis", "carotid thrombosis", "THROMBOSIS CAROTID", "CAROTID THROMBOSIS", "Thrombosis, Carotid", "thrombosis; carotid", "carotid; thrombosis", "a.carotis; thrombosis", "Carotid artery thrombosis", "Carotid Artery Thromboses", "carotid artery thrombosis", "THROMBOSIS CAROTID ARTERY", "Carotid Artery Thrombosis", "carotid artery thromboses", "artery carotid thrombosis", "Thrombosis carotid artery", "Thrombosis, Carotid Artery", "thrombosis; carotid artery", "Carotid artery thrombosis (disorder)", "carotid artery thrombosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carotid artery thrombosis", "shortest_name_length": 18}
{"curie": "MONDO:0021742", "names": ["Puerperal Infection", "Puerperal infection", "puerperal infection", "Infection;puerperal", "PUERPERAL INFECTION", "Puerperal infections", "Puerperal Infections", "puerperal; infection", "infection; puerperal", "Infection, Puerperal", "Infections, Puerperal", "puerperal infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "puerperal infection", "shortest_name_length": 19}
{"curie": "MONDO:0008879", "names": ["BWCNS", "Hutterite syndrome", "Bowen-Conradi syndrome", "BOWEN-CONRADI SYNDROME", "Bowen Hutterite syndrome", "Bowen syndrome, Hutterite type", "Bowen-Conradi Hutterite syndrome", "Bowen-Conradi syndrome (disorder)", "BOWEN HUTTERITE SYNDROME, FORMERLY", "Bowen Hutterite syndrome, formerly", "Bowen Hutterite syndrome (formerly)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bowen-Conradi syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0235802", "names": ["Impaired pupillary reflex", "Pupillary reflex impaired", "PUPILLARY REFLEX IMPAIRED", "Impaired pupillary reflex (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Impaired pupillary reflex", "shortest_name_length": 25}
{"curie": "MONDO:0012730", "names": ["Aat6", "AAT6", "aortic aneurysm, familial thoracic 6", "Aortic Aneurysm, Familial Thoracic 6", "AORTIC ANEURYSM, FAMILIAL THORACIC 6", "aortic aneurysm, familial thoracic type 6", "ACTA2 familial thoracic aortic aneurysm and aortic dissection", "Familial Thoracic Aortic Aneurysm With Livedo Reticularis And Iris Flocculi", "FAMILIAL THORACIC AORTIC ANEURYSM WITH LIVEDO RETICULARIS AND IRIS FLOCCULI", "familial thoracic aortic aneurysm with livedo reticularis and iris flocculi", "familial thoracic aortic aneurysm and aortic dissection caused by mutation in ACTA2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic aneurysm, familial thoracic 6", "shortest_name_length": 4}
{"curie": "UMLS:C0751569", "names": ["Urogenital Cancer", "Cancer, Urogenital", "Urogenital Cancers", "Cancers, Urogenital", "Genitourinary Cancer", "Genitourinary Cancers", "Cancer, Genitourinary", "Genito-urinary Cancer", "Genito urinary Cancer", "Cancers, Genitourinary", "Cancer, Genito-urinary", "Genito-urinary Cancers", "Cancers, Genito-urinary", "Genitourinary System Cancer", "Malignant Genitourinary Neoplasm", "Malignant Genitourinary System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Genitourinary Cancer", "shortest_name_length": 17}
{"curie": "MONDO:0010684", "names": ["XMEA", "MEAX", "Vacuolar myopathy", "vacuolar myopathy", "Autophagic vacuolar myopathy", "X-linked myopathy with excessive autophagy", "Myopathy, X-Linked, with Excessive Autophagy", "myopathy, X-linked, with excessive autophagy", "MYOPATHY, X-LINKED, WITH EXCESSIVE AUTOPHAGY", "Myopathy, Autophagic Vacuolar, Infantile-Onset", "MYOPATHY, AUTOPHAGIC VACUOLAR, INFANTILE-ONSET", "X-linked myopathy with excessive autophagy (disorder)", "myopathy, X-linked, with excessive autophagy, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked myopathy with excessive autophagy", "shortest_name_length": 4}
{"curie": "UMLS:C0394996", "names": ["drunk", "Drunk", "drunks", "Drink Dosing Unit", "Intoxication;alcohol;acute", "Acute alcohol intoxication", "Alcohol intoxication acute", "acute alcohol intoxication", "Acute alcohol overingestion", "Alcohol intoxication, acute", "Acute Alcoholic Intoxication", "Acute alcoholic intoxication", "acute alcoholic intoxication", "Acute alcohol intoxication (disorder)", "Mental and behavioral disorders due to use of alcohol, acute intoxication", "Mental and behavioural disorders due to use of alcohol, acute intoxication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute alcoholic intoxication", "shortest_name_length": 5}
{"curie": "UMLS:C1707406", "names": ["Clear Cell Intrahepatic Cholangiocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clear Cell Intrahepatic Cholangiocarcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0019421", "names": ["X-linked intellectual disability Seemanova type", "X-linked intellectual disability, Seemanova type", "X-linked intellectual disability Seemanova type (disorder)", "X-linked intellectual disability Seemanova type (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability, Seemanova type", "shortest_name_length": 47}
{"curie": "MONDO:0021358", "names": ["hypopharynx tumor", "Tumor of hypopharynx", "Hypopharyngeal Tumor", "Tumor of Hypopharynx", "hypopharyngeal tumor", "hypopharynx neoplasm", "tumor of hypopharynx", "Tumour of hypopharynx", "Neoplasm of hypopharynx", "Neoplasm of Hypopharynx", "hypopharyngeal neoplasm", "Tumor of laryngopharynx", "neoplasm of hypopharynx", "Hypopharyngeal Neoplasm", "Hypopharyngeal neoplasm", "tumor of the hypopharynx", "hypopharyngeal neoplasms", "Hypopharyngeal Neoplasms", "Neoplasm, Hypopharyngeal", "Tumor of the Hypopharynx", "Tumour of laryngopharynx", "Neoplasms, Hypopharyngeal", "neoplasm of the hypopharynx", "Neoplasm of the Hypopharynx", "hypopharynx neoplasm (disease)", "Neoplasm of hypopharynx (disorder)", "neoplasm of hypopharynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplasm of hypopharynx", "shortest_name_length": 17}
{"curie": "MONDO:0014620", "names": ["DYT26", "myoclonic dystonia 26", "dystonia 26, myoclonic", "DYSTONIA 26, MYOCLONIC", "myoclonic dystonia type 26", "KCTD17 myoclonus-dystonia syndrome", "myoclonus-dystonia syndrome caused by mutation in KCTD17"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myoclonic dystonia 26", "shortest_name_length": 5}
{"curie": "MONDO:0015130", "names": ["acquired chronic primary adrenal insufficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired chronic primary adrenal insufficiency", "shortest_name_length": 46}
{"curie": "MONDO:0026765", "names": ["CDG2R", "CDGIIR", "CDG IIr", "congenital disorder of glycosylation, type IIr", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIr", "congenital disorder of glycosylation, type IIr, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital disorder of glycosylation, type IIr", "shortest_name_length": 5}
{"curie": "MONDO:0021254", "names": ["Uterine Body Tumor", "Corpus Uteri Tumor", "uterine body tumor", "corpus uteri tumor", "Uterine Corpus Tumor", "body of uterus tumor", "uterine corpus tumor", "Tumor of Uterine Body", "tumor of uterine body", "tumor of corpus uteri", "corpus uteri neoplasm", "Tumor of Corpus Uteri", "Uterine Body Neoplasm", "uterine body neoplasm", "Corpus Uteri Neoplasm", "tumor of uterine corpus", "body of uterus neoplasm", "uterine corpus neoplasm", "Uterine Corpus Neoplasm", "tumor of body of uterus", "Tumor of Uterine Corpus", "neoplasm of corpus uteri", "neoplasm of uterine body", "Neoplasm of Corpus Uteri", "Neoplasm of Uterine Body", "Tumor of the Corpus Uteri", "Tumor of the Uterine Body", "tumor of the uterine body", "tumor of the corpus uteri", "neoplasm of body of uterus", "Neoplasm of Uterine Corpus", "Neoplasm of Body of Uterus", "neoplasm of uterine corpus", "Neoplasm of body of uterus", "Tumor of the Uterine Corpus", "tumor of the uterine corpus", "Neoplasm of the Uterine Body", "neoplasm of the uterine body", "Neoplasm of the Corpus Uteri", "neoplasm of the corpus uteri", "neoplasm of the body of uterus", "Neoplasm of the Uterine Corpus", "neoplasm of the uterine corpus", "Neoplasm of the Body of Uterus", "body of uterus neoplasm (disease)", "Neoplasm of body of uterus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corpus uteri neoplasm", "shortest_name_length": 18}
{"curie": "UMLS:C1333056", "names": ["Classic Lymphocytic Colitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Classic Lymphocytic Colitis", "shortest_name_length": 27}
{"curie": "UMLS:C4743636", "names": ["Unresectable Renal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Renal Cell Carcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C1531510", "names": ["Bacterial endophthalmitis", "Bacterial Endophthalmitis", "endophthalmitis bacterial", "Bacterial endophthalmitis (disorder)", "Bacterial endophthalmitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bacterial endophthalmitis", "shortest_name_length": 25}
{"curie": "MONDO:0006170", "names": ["conjunctiva disease", "disease conjunctiva", "conjunctiva diseases", "conjunctival disease", "disease conjunctival", "Conjunctival Disease", "Disease, Conjunctival", "conjunctival diseases", "Conjunctival Diseases", "Conjunctival Disorder", "Conjunctival disorder", "conjunctiva; disorder", "conjunctival disorder", "Conjunctiva--Diseases", "conjunctival disorders", "Disease of conjunctiva", "disease of conjunctiva", "Diseases, Conjunctival", "disorder of conjunctiva", "Disorder of conjunctiva", "Disorders of conjunctiva", "Conjunctival disorder NOS", "Disorder of conjunctiva, NOS", "DISORDERS OF THE CONJUNCTIVA", "conjunctiva disease or disorder", "conjunctival disorder (diagnosis)", "Disorders of conjunctiva (H10-H11)", "Disorder of conjunctiva (disorder)", "disease (or disorder); conjunctiva", "disease or disorder of conjunctiva", "Unspecified disorder of conjunctiva", "Disorder of conjunctiva, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "conjunctival disorder", "shortest_name_length": 19}
{"curie": "MONDO:0020663", "names": ["Spindle Cell Cancer", "spindle cell cancer", "spindle cell type neoplasm", "malignant spindle cell tumor", "Malignant Spindle Cell Tumor", "Malignant Spindle Cell Neoplasm", "malignant spindle cell neoplasm", "Malignant tumor, spindle cell type", "Malignant tumor, fusiform cell type", "Malignant tumour, spindle cell type", "Malignant tumor - spindle cell type", "Malignant tumour, fusiform cell type", "Malignant tumour - spindle cell type", "Malignant tumor - fusiform cell type", "Malignant tumour - fusiform cell type", "tumor; fusiform cell (type), malignant", "tumor; malignant, fusiform cell (type)", "spindle cell type neoplasm (diagnosis)", "Malignant tumor, fusiform cell type (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant spindle cell neoplasm", "shortest_name_length": 19}
{"curie": "MONDO:0500018", "names": ["AFOP", "acute fibrinous and organizing pneumonia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute fibrinous and organizing pneumonia", "shortest_name_length": 4}
{"curie": "MONDO:0016281", "names": ["SRXX1", "OVOTESTICULAR DSD", "Ovotesticular DSD", "ovotesticular DSD", "DSD, Ovotesticular", "Ovotesticular DSDs", "DSDs, Ovotesticular", "true hermaphroditism", "True Hermaphroditism", "46,XX Sex Reversal 1", "46,XX SEX REVERSAL 1", "XX MALE, SRY-POSITIVE", "XX Male, SRY-Positive", "46,XX ovotesticular DSD", "XX Male Syndrome, Sry-Positive", "XX Male Syndrome, Sry Positive", "46,XX SEX REVERSAL, SRY-POSITIVE", "46,XX TRUE HERMAPHRODITISM, SRY-POSITIVE", "46,XX True Hermaphroditism, Sry-Positive", "Ovotesticular disorder of sex development", "Ovotesticular Disorder Of Sex Development", "OVOTESTICULAR DISORDER OF SEX DEVELOPMENT", "Ovotesticular Disorders of Sex Development", "ovotesticular disorders of sex development", "46,XX TESTICULAR DISORDER OF SEX DEVELOPMENT", "Ovotesticular Differences of Sex Development", "ovotesticular differences of sex development", "46,XX ovotesticular disorder of sex development", "46,XX GONADAL DYSGENESIS, COMPLETE, SRY-POSITIVE", "46,XX Gonadal Dysgenesis, Complete, Sry-Positive", "Ovotesticular disorder of sex development (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XX ovotesticular disorder of sex development", "shortest_name_length": 5}
{"curie": "MONDO:0013249", "names": ["DFNB84", "DFNB84A", "DEAFNESS, AUTOSOMAL RECESSIVE 84", "deafness, autosomal recessive 84", "autosomal recessive deafness 84A", "DEAFNESS, AUTOSOMAL RECESSIVE 84A", "deafness, autosomal recessive 84a", "deafness, autosomal recessive 84A", "deafness, autosomal recessive type 84A", "autosomal recessive nonsyndromic deafness 84A", "PTPRQ autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 84A", "autosomal recessive nonsyndromic deafness type 84A", "autosomal recessive deafness 84A with vestibular dysfunction", "deafness, autosomal recessive 84A, with vestibular dysfunction", "DEAFNESS, AUTOSOMAL RECESSIVE 84A, WITH VESTIBULAR DYSFUNCTION", "autosomal recessive nonsyndromic deafness caused by mutation in PTPRQ"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 84A", "shortest_name_length": 6}
{"curie": "MONDO:0003499", "names": ["Pseudosarcoma of skin", "Pseudosarcoma of the skin", "Epidermoid Spindle Cell Carcinoma", "Epidermoid carcinoma, spindle cell", "Sarcomatoid Squamous Cell Carcinoma", "Epidermoid carcinoma - spindle cell", "Sarcomatoid squamous cell carcinoma", "squamous cell carcinoma, sarcomatoid", "Spindle Cell Squamous Cell Carcinoma", "Squamous Cell Carcinoma, Sarcomatoid", "Squamous cell carcinoma, sarcomatoid", "spindle cell squamous cell carcinoma", "Squamous Cell Spindle Cell Carcinoma", "Spindle cell squamous cell carcinoma", "Squamous Cell Carcinoma, Spindle Cell", "Squamous cell carcinoma, spindle cell", "Squamous cell carcinoma - spindle cell", "Spindle cell squamous carcinoma of skin", "Epidermoid carcinoma, spindle cell type", "spindle cell squamous carcinoma of skin", "Spindle Cell Squamous Carcinoma of Skin", "sarcomatoid squamous cell skin carcinoma", "Skin Spindle Cell Squamous Cell Carcinoma", "Squamous cell carcinoma, spindle cell type", "Spindle Cell Squamous Carcinoma of the Skin", "spindle cell squamous carcinoma of the skin", "skin neoplasm carcinoma squamous spindle cell", "Squamous Cell Carcinoma, Spindle Cell Variant", "Skin Pseudosarcomatous Squamous Cell Carcinoma", "Spindle cell squamous cell carcinoma (disorder)", "spindle cell squamous cell carcinoma (diagnosis)", "spindle cell (sarcomatoid) squamous cell carcinoma", "Spindle Cell (Sarcomatoid) Squamous Cell Carcinoma", "Spindle cell squamous carcinoma of skin (disorder)", "Spindle cell squamous carcinoma of skin (diagnosis)", "Spindle Cell (Sarcomatoid) Squamous Cell Skin Carcinoma", "spindle cell (sarcomatoid) squamous cell skin carcinoma", "Skin Spindle Cell (Sarcomatoid) Squamous Cell Carcinoma", "Squamous cell carcinoma, spindle cell (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sarcomatoid squamous cell skin carcinoma", "shortest_name_length": 21}
{"curie": "MONDO:0100283", "names": ["overgrowth syndrome and/or cerebral malformations due to abnormalities in MTOR pathway genes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "overgrowth syndrome and/or cerebral malformations due to abnormalities in MTOR pathway genes", "shortest_name_length": 92}
{"curie": "MONDO:0002071", "names": ["Supratentorial Tumor", "Tumor, Supratentorial", "Supratentorial Tumors", "supratentorial cancer", "Supratentorial Cancer", "Supratentorial Cancers", "Tumors, Supratentorial", "Cancer, Supratentorial", "Supratentorial neoplasm", "Supratentorial Neoplasm", "Cancers, Supratentorial", "Pineal parenchymal tumor", "Supratentorial Neoplasms", "Neoplasm, Supratentorial", "Pineal parenchymal tumour", "Neoplasms, Supratentorial", "malignant supratentorial tumor", "brain neoplasm, supratentorial", "malignant Supratentorial tumor", "Malignant Supratentorial Tumor", "Brain neoplasm, Supratentorial", "Brain Neoplasms, Supratentorial", "malignant supratentorial neoplasm", "Malignant Supratentorial Neoplasm", "Supratentorial Neoplasm, Malignant", "Malignant Supratentorial Neoplasms", "Neoplasm, Malignant Supratentorial", "Neoplasms, Malignant Supratentorial", "Supratentorial Neoplasms, Malignant", "supratentorial neoplasms, malignant", "Malignant Supratentorial Brain Tumor", "Malignant neoplasm of supratentorial NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "supratentorial cancer", "shortest_name_length": 20}
{"curie": "UMLS:C4086170", "names": ["Childhood Seminoma", "Childhood Testicular Germinomatous Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Seminoma", "shortest_name_length": 18}
{"curie": "UMLS:C4329270", "names": ["Acute Myeloid Leukemia with Monoallelic Mutations of CEBPA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Myeloid Leukemia with Monoallelic Mutations of CEBPA", "shortest_name_length": 58}
{"curie": "UMLS:C1336422", "names": ["Stage IV Lip Cancer", "Stage IV Cancer of Lip", "Stage IV Lip Carcinoma", "Stage IV Carcinoma of Lip", "Stage IV Cancer of the Lip", "Stage IV Lip Cancer AJCC v6", "Stage IV Lip Cancer AJCC v7", "Stage IV Carcinoma of the Lip", "Stage IV Lip Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Lip Cancer AJCC v6 and v7", "shortest_name_length": 19}
{"curie": "UMLS:C0858677", "names": ["Nephritis allergic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephritis allergic", "shortest_name_length": 18}
{"curie": "MONDO:0010600", "names": ["CGD", "CDGX", "CGDX", "X-linked chronic granulomatous disease", "X-linked Chronic Granulomatous Disease", "X Linked Chronic Granulomatous Disease", "X-Linked Chronic Granulomatous Disease", "Chronic Granulomatous Disease, X Linked", "Chronic Granulomatous Disease, Atypical", "CHRONIC GRANULOMATOUS DISEASE, X-LINKED", "chronic granulomatous disease, X-linked", "CHRONIC GRANULOMATOUS DISEASE, ATYPICAL", "Chronic Granulomatous Disease, X-Linked", "chronic granulomatous disease, atypical", "granulomatous disease, chronic, X-linked", "Granulomatous Disease, Chronic, X-Linked", "GRANULOMATOUS DISEASE, CHRONIC, X-LINKED", "granulomatous disease, chronic, X-linked, variant", "GRANULOMATOUS DISEASE, CHRONIC, X-LINKED, VARIANT", "Granulomatous Disease, Chronic, X-Linked, Variant", "Granulomatous Disease, Chronic, Autosomal Dominant Type", "granulomatous disease, chronic, autosomal dominant type", "chronic granulomatous disease, X-linked, X-linked recessive", "X-linked chronic cytochrome b-negative granulomatous disease", "cytochrome B-positive granulomatous disease, chronic, X-linked", "CYTOCHROME b-POSITIVE GRANULOMATOUS DISEASE, CHRONIC, X-LINKED", "Cytochrome B-Positive Granulomatous Disease, Chronic, X-Linked", "CYTOCHROME b-NEGATIVE GRANULOMATOUS DISEASE, CHRONIC, X-LINKED", "cytochrome B-negative granulomatous disease, chronic, X-linked", "Cytochrome B-Negative Granulomatous Disease, Chronic, X-Linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "granulomatous disease, chronic, X-linked", "shortest_name_length": 3}
{"curie": "UMLS:C1334552", "names": ["Major Salivary Gland Non-Hodgkin Lymphoma", "Major Salivary Gland Non-Hodgkin's Lymphoma", "Non-Hodgkin's Lymphoma of Major Salivary Gland", "Non-Hodgkin's Lymphoma of the Major Salivary Gland", "Primary Major Salivary Gland Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Major Salivary Gland Non-Hodgkin Lymphoma", "shortest_name_length": 41}
{"curie": "UMLS:C1335500", "names": ["Proliferating Breast Lesion without Atypia", "Proliferating Lesion of Breast without Atypia", "Proliferating Lesion of the Breast without Atypia", "Breast Fibrocystic Change, Proliferative Type without Atypia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Fibrocystic Change, Proliferative Type without Atypia", "shortest_name_length": 42}
{"curie": "MONDO:0043089", "names": ["AMPPE", "apmppe", "APMPPE", "acute placoid pigment epitheliopathy", "multifocal placoid pigment epitheliopathy", "Acute multifocal placoid pigment epitheliopathy", "acute multifocal placoid pigment epitheliopathy", "AMPPE - Acute multifocal placoid pigment epitheliopathy", "amppe - acute multifocal placoid pigment epitheliopathy", "acute posterior multifocal placoid pigment epitheliopathy", "Acute posterior multifocal placoid pigment epitheliopathy", "Acute Posterior Multifocal Placoid Pigment Epitheliopathy", "epitheliopathy, acute posterior multifocal placoid pigment", "Acute multifocal placoid pigment epitheliopathy (disorder)", "pigment epitheliopathy, disseminated retinitis and retinochoroiditis", "Disseminated retinitis and retinochoroiditis, pigment epitheliopathy", "Pigment epitheliopathy, disseminated retinitis and retinochoroiditis", "Pigment epitheliopathy, disseminated retinitis AND retinochoroiditis", "acute posterior multifocal placoid pigment epitheliopathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute posterior multifocal placoid pigment epitheliopathy", "shortest_name_length": 5}
{"curie": "MONDO:0015291", "names": ["Stromal keratitis", "stromal keratitis", "stromal keratitis (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stromal keratitis", "shortest_name_length": 17}
{"curie": "MONDO:0006544", "names": ["fifth disease", "Fifth Disease", "Disease;Fifth", "Fifth disease", "FIFTH DISEASE", "fifth; disease", "slap cheek syndrome", "erythema contagiosum", "Erythema infectiosum", "Erythema Infectiosum", "Erythema contagiosum", "erythema infectiosum", "ERYTHEMA INFECTIOSUM", "Erythema;infectiosum", "erythema; infectiosum", "infectiosum; erythema", "ertythema infectiosum", "slapped cheek syndrome", "Slapped cheek syndrome", "parvovirus b19 infection", "Parvovirus B19 infection", "parvovirus B19 infection", "Parvovirus B19 Infection", "Infection, Parvovirus B19", "Parvovirus B19 Infections", "erythema infectiosum (diagnosis)", "erythema infectiosum (fifth disease)", "Erythema Infectiosum (Fifth Disease)", "Erythema infectiosum [fifth disease]", "parvovirus B19 infection (diagnosis)", "disease (or disorder); fifth disease", "Erythema infectiosum (fifth disease)", "Primate erythroparvovirus 1 infection", "Primate erythroparvovirus 1 infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythema infectiosum", "shortest_name_length": 13}
{"curie": "UMLS:C2828187", "names": ["Stage IIB Gestational Trophoblastic Tumor", "Stage IIB Gestational Trophoblastic Tumor AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Gestational Trophoblastic Tumor AJCC v7", "shortest_name_length": 41}
{"curie": "UMLS:C0020457", "names": ["hhnc", "nkhhc", "Hyperosmolar coma", "hyperosmolar coma", "HYPEROSMOLAR COMA", "coma hyperosmolar", "hyperosmolar; coma", "coma; hyperosmolar", "Diabetic hyperosmolar coma", "diabetic hyperosmolar coma", "Hyperosmolar Nonketotic Coma", "nonketotic hyperosmolar coma", "hyperosmolar nonketotic coma", "Hyperosmolar nonketotic coma", "Nonketotic Hyperosmolar Coma", "Nonketotic Hyperosmolar Comas", "Hyperosmolar Nonketotic Comas", "Nonketotic Hyperglycemic Coma", "Coma, Hyperosmolar Nonketotic", "Hyperosmolar Coma, Nonketotic", "Coma, Nonketotic Hyperosmolar", "NON-KETOTIC HYPEROSMOLAR COMA", "hyperosmolar non-ketotic coma", "Nonketotic Coma, Hyperosmolar", "Nonketotic Comas, Hyperosmolar", "Hyperglycemic Coma, Nonketotic", "Comas, Nonketotic Hyperosmolar", "Coma, Nonketotic Hyperglycemic", "Comas, Hyperosmolar Nonketotic", "Hyperosmolar Comas, Nonketotic", "Hyperosmolar (non-ketotic) coma", "Diabetes with hyperosmolar coma", "DIABETIC NONKETOTIC HYPEROSMOLAR COMA", "Hyperosmolar non-ketotic diabetic coma", "Hyperosmolar nonketotic coma in diabetes", "Hyperosmolar Hyperglycemic Nonketotic Coma", "Nonketotic hyperglycemic-hyperosmolar coma", "Hyperglycemic Hyperosmolar Nonketotic Coma", "Nonketotic hyperglycaemic-hyperosmolar coma", "Coma, Hyperglycemic Hyperosmolar Nonketotic", "diabetic hyperosmolar nonketotic state with coma", "diabetes mellitus with hyperglycemic hyperosmolar nonketotic state with coma", "diabetes mellitus with hyperglycemic hyperosmolar nonketotic state with coma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyperglycemic Hyperosmolar Nonketotic Coma", "shortest_name_length": 4}
{"curie": "UMLS:C0079741", "names": ["intermediate-grade lymphoma", "Intermediate-Grade Lymphoma", "Intermediate grade lymphoma", "Intermediate Grade Lymphoma", "Lymphoma, Intermediate-Grade", "Intermediate-Grade Lymphomas", "Lymphoma, Intermediate Grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoma, Intermediate-Grade", "shortest_name_length": 27}
{"curie": "MONDO:0006297", "names": ["maxillary sinus adenoid cystic carcinoma", "Maxillary Sinus Adenoid Cystic Carcinoma", "adenoid cystic carcinoma of maxillary sinus", "Adenoid Cystic Carcinoma of Maxillary Sinus", "adenoid cystic carcinoma of the maxillary sinus", "Adenoid Cystic Carcinoma of the Maxillary Sinus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maxillary sinus adenoid cystic carcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0016914", "names": ["partial deletion of chromosome 16q", "partial monosomy of chromosome 16q", "partial deletion of the long arm of chromosome 16", "partial monosomy of the long arm of chromosome 16", "partial deletion of the long arm of chromosome type 16"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of the long arm of chromosome 16", "shortest_name_length": 34}
{"curie": "UMLS:C0236988", "names": ["Schizophrenia and Other Psychotic Disorders", "Schizophrenia and other psychotic disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Schizophrenia and other psychotic disorders", "shortest_name_length": 43}
{"curie": "MONDO:0600010", "names": ["moderate hypophosphatasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "moderate hypophosphatasia", "shortest_name_length": 25}
{"curie": "MONDO:0001089", "names": ["acute inferolateral myocardial infarction", "Acute inferolateral myocardial infarction", "Acute myocardial infarction of inferolateral wall", "acute myocardial infarction of inferolateral wall", "Acute myocardial infarction, of inferolateral wall", "acute inferolateral myocardial infarction (diagnosis)", "Acute myocardial infarction of inferolateral wall (disorder)", "Acute myocardial infarction of inferolateral wall, episode of care unspecified", "Acute myocardial infarction, of inferolateral wall, episode of care unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute inferolateral myocardial infarction", "shortest_name_length": 41}
{"curie": "UMLS:C0340990", "names": ["rejection; graft, bone marrow", "Rejection of bone marrow graft", "BONE MARROW TRANSPLANT REJECTION", "Bone marrow transplant rejection", "bone marrow transplant rejection", "Bone-marrow transplant rejection", "bone marrow transplant; rejection", "rejection; transplant, bone marrow", "Bone marrow transplant rejection (disorder)", "bone marrow transplant rejection (diagnosis)", "complications bone marrow transplant rejection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone marrow transplant rejection", "shortest_name_length": 29}
{"curie": "UMLS:C4725839", "names": ["Infiltrating Bladder Cancer", "Infiltrating Bladder Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infiltrating Bladder Carcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0013693", "names": ["NISBD1", "INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 1", "inflammatory skin and bowel disease, neonatal, 1", "ADAM17 neonatal inflammatory skin and bowel disease", "inflammatory skin and bowel disease, neonatal, type 1", "neonatal inflammatory skin and bowel disease caused by mutation in ADAM17"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory skin and bowel disease, neonatal, 1", "shortest_name_length": 6}
{"curie": "MONDO:0005198", "names": ["vin", "VIN", "vulva dysplasia", "dysplasia vulvar", "dysplasia; vulva", "Vulvar dysplasia", "vulval dysplasia", "vulvar dysplasia", "vulva; dysplasia", "cancer situ vulvar", "Dysplasia of vulva", "dysplasia of vulva", "carcinoma situ vulva", "vulvar cancer in situ", "dysplasia of the vulva", "Vulvar intraepithelial tumor", "vulvar intraepithelial tumor", "Dysplasia of vulva (disorder)", "dysplasia of vulva (diagnosis)", "Vulva Intraepithelial Neoplasia", "Dysplasia of vulva, unspecified", "vulva intraepithelial neoplasia", "vulvar intraepithelial neoplasia", "Vulvar intraepithelial neoplasia", "Vulval intraepithelial neoplasia", "Vulval Intraepithelial Neoplasia", "vulva; intraepithelial neoplasia", "Vulvar Intraepithelial Neoplasia", "vulval intraepithelial neoplasia", "neoplasia; intraepithelial, vulva", "intraepithelial neoplasia of vulva", "Intraepithelial Neoplasia of Vulva", "VIN - Vulval intraepithelial neoplasia", "Vulval intraepithelial neoplasia (VIN)", "Intraepithelial Neoplasia of the Vulva", "intraepithelial neoplasia of the vulva", "Squamous Vulvar Intraepithelial Neoplasia", "squamous vulvar intraepithelial neoplasia", "Vulval intraepithelial neoplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar intraepithelial neoplasia", "shortest_name_length": 3}
{"curie": "MONDO:0004231", "names": ["spindle cell variant squamous cell breast carcinoma", "Squamous Cell Breast Carcinoma, Spindle Cell Variant", "squamous cell breast carcinoma, spindle cell variant", "Breast Squamous Cell Carcinoma, Spindle Cell Variant", "metaplastic adenocarcinoma with spindle cell differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spindle cell variant squamous cell breast carcinoma", "shortest_name_length": 51}
{"curie": "MONDO:0000429", "names": ["autosomal genetic disease", "autosomal inherited disease", "autosomal inherited disorder", "Autosomal hereditary disorder", "autosomal hereditary disorder", "Hereditary disorder, autosomal", "Autosomal hereditary disorder, NOS", "inherited genetic conditions autosomal", "Autosomal hereditary disorder (disorder)", "autosomal hereditary disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal genetic disease", "shortest_name_length": 25}
{"curie": "MONDO:0000119", "names": ["CHTD", "congenital heart defects, multiple types"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital heart defects, multiple types", "shortest_name_length": 4}
{"curie": "UMLS:C4016951", "names": ["BREAST CANCER, EARLY-ONSET", "Breast cancer, early-onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "BREAST CANCER, EARLY-ONSET", "shortest_name_length": 26}
{"curie": "MONDO:0008887", "names": ["BESC1", "bronchiectasis 1", "cystic fibrosis-like syndrome", "CYSTIC FIBROSIS-LIKE SYNDROME", "Bronchiectasis With Or Without Elevated Sweat Chloride 1", "BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 1", "bronchiectasis with or without elevated sweat chloride 1", "bronchiectasis with or without elevated sweat chloride type 1", "bronchiectasis with or without elevated sweat chloride 1, modifier of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bronchiectasis with or without elevated sweat chloride 1", "shortest_name_length": 5}
{"curie": "MONDO:0016981", "names": ["infantile spams-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome", "infantile spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile spams-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome", "shortest_name_length": 96}
{"curie": "MONDO:0005352", "names": ["Conduct Disorder", "Disorder;conduct", "CONDUCT DISORDER", "Conduct disorder", "conduct disorder", "conduct disorders", "Conduct disorders", "Conduct Disorders", "Conduct disorder NOS", "Conduct behavior disorder", "Conduct behaviour disorder", "Conduct disorder (disorder)", "conduct disorder (diagnosis)", "Conduct disorder, unspecified", "Unspecified disturbance of conduct"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "conduct disorder", "shortest_name_length": 16}
{"curie": "UMLS:C2931210", "names": ["Usher syndrome type 1F", "Usher syndrome, type 1F", "Usher syndrome type 1F (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Usher syndrome, type 1F", "shortest_name_length": 22}
{"curie": "MONDO:0005086", "names": ["rcc", "RCC", "rccs", "Grawitz tumor", "Hypernephroma", "hypernephroma", "grawitz tumor", "Grawitz tumour", "Renal Carcinoma", "RENAL CARCINOMA", "carcinoma renal", "Renal carcinoma", "renal carcinoma", "Renal Carcinomas", "Carcinoma;kidney", "Carcinoma, Renal", "kidney carcinoma", "carcinomas renal", "carcinoma kidney", "Renal Cell Cancer", "Renal cell cancer", "renal cell cancer", "cell renal cancer", "cancer cell renal", "Renal Cell Cancers", "cancer cells renal", "Cancer, Renal Cell", "Nephroid Carcinoma", "carcinoma of kidney", "Carcinoma, Nephroid", "of kidney carcinoma", "Nephroid Carcinomas", "renal adenocarcinoma", "carcinoma cell renal", "adenocarcinoma renal", "Renal Adenocarcinoma", "Renal Cell Carcinoma", "Renal adenocarcinoma", "renal cell carcinoma", "RENAL CELL CARCINOMA", "Renal cell carcinoma", "carcinoma; renal cell", "renal cell; carcinoma", "Renal Adenocarcinomas", "Carcinoma, Renal Cell", "Adenocarcinoma, Renal", "Kidney Adenocarcinoma", "kidney adenocarcinoma", "Renal Cell Carcinomas", "carcinoma cells renal", "Carcinomas, Renal Cell", "adenocarcinoma kidneys", "Adenocarcinoma of kidney", "Adenocarcinoma of Kidney", "Adenocarcinoma Of Kidney", "ADENOCARCINOMA OF KIDNEY", "adenocarcinoma of kidney", "Renal cell carcinoma NOS", "hypernephroid carcinomas", "renal cell adenocarcinoma", "Adenocarcinoma Of Kidneys", "Renal cell adenocarcinoma", "Kidney, Adenocarcinoma Of", "Renal Cell Adenocarcinoma", "Renal Cell Adenocarcinomas", "renal cell; adenocarcinoma", "adenocarcinoma; renal cell", "adenocarcinoma cells renal", "Adenocarcinoma, Renal Cell", "Adenocarcinomas, Renal Cell", "adenocarcinoma of the kidney", "RENAL CANCER, ADENOCARCINOMA", "Adenocarcinoma of the Kidney", "renal cell carcinoma (disease)", "Renal cell carcinoma (disorder)", "renal cell carcinoma (diagnosis)", "Renal cell carcinoma - morphology", "Adenocarcinoma of kidney (disorder)", "adenocarcinoma of kidney (diagnosis)", "Renal cell carcinoma stage unspecified", "renal cell carcinoma, stage unspecified", "Renal Cell Carcinoma, Stage Unspecified", "Cancer starting in small tubes in kidneys", "Renal cell carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal cell carcinoma", "shortest_name_length": 3}
{"curie": "MONDO:0100477", "names": ["disorder of methylamine metabolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of methylamine metabolism", "shortest_name_length": 34}
{"curie": "MONDO:0001310", "names": ["Bowman membrane folds or rupture", "Bowman's membrane folds or rupture", "Folds and rupture of bowman's membrane", "Folds and rupture of Bowman's membrane", "Folds and rupture in Bowman's membrane", "folds and rupture of Bowman's membrane", "folds and rupture in bowman's membrane", "Folds AND/OR rupture of Bowman membrane", "Folds AND/OR rupture of Bowman's membrane", "folds and/or rupture of bowman's membrane", "folds and rupture in bowman's membrane (diagnosis)", "Folds AND/OR rupture of Bowman's membrane (disorder)", "folds and rupture of Bowman's membrane (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bowman's membrane folds or rupture", "shortest_name_length": 32}
{"curie": "MONDO:0019742", "names": ["late-onset nephronophthisis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "late-onset nephronophthisis", "shortest_name_length": 27}
{"curie": "MONDO:0030302", "names": ["IMD81", "immunodeficiency 81", "IMMUNODEFICIENCY 81", "T-B+ severe combined immunodeficiency due to SLP76 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 81", "shortest_name_length": 5}
{"curie": "MONDO:0023664", "names": ["SPGF54", "spermatogenic failure 54", "SPERMATOGENIC FAILURE 54"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 54", "shortest_name_length": 6}
{"curie": "UMLS:C0456844", "names": ["myeloma light chain", "Light chain myeloma", "light chain myeloma", "Light Chain Myeloma", "Light Chain Multiple Myeloma", "Light chain myeloma (disorder)", "Light chain myeloma (diagnosis)", "malignant neoplasm multiple myeloma light chain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Light chain myeloma", "shortest_name_length": 19}
{"curie": "UMLS:C1112573", "names": ["delay orgasm", "delay orgasms", "Delayed Orgasm", "delayed orgasm", "Delayed orgasm", "orgasm; delayed", "delayed; orgasm", "delayed orgasm (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Delayed Orgasm", "shortest_name_length": 12}
{"curie": "UMLS:C1096343", "names": ["Infusion site reaction", "Infusion Site Reaction", "Infusion Site Reactions", "Infusion site reactions", "Infusion Site Adverse Event", "Infusion Site Adverse Reaction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infusion site reaction", "shortest_name_length": 22}
{"curie": "UMLS:C4744566", "names": ["Metastatic Rectal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Rectal Carcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C0347396", "names": ["Benign Skin Vascular Tumor", "Benign Skin Vascular Neoplasm", "Benign Cutaneous Vascular Tumor", "Benign cutaneous vascular tumor", "Benign cutaneous vascular tumour", "Benign Cutaneous Vascular Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Skin Vascular Neoplasm", "shortest_name_length": 26}
{"curie": "MONDO:0011402", "names": ["CCFDN", "Congenital cataracts, facial dysmorphism and neuropathy", "CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY", "congenital cataracts, facial dysmorphism, and neuropathy", "Congenital Cataracts, Facial Dysmorphism, And Neuropathy", "congenital cataracts-facial dysmorphism-neuropathy syndrome", "Congenital cataracts-facial dysmorphism-neuropathy syndrome", "Cataract, Congenital, With Facial Dysmorphism And Neuropathy", "cataract, congenital, with Facial Dysmorphism and neuropathy", "CATARACT, CONGENITAL, WITH FACIAL DYSMORPHISM AND NEUROPATHY", "CCFDN - congenital cataracts, facial dysmorphism and neuropathy", "Congenital cataracts, facial dysmorphism and neuropathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital cataracts-facial dysmorphism-neuropathy syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0006040", "names": ["lactacidosis", "Lacticacidosis", "Lacticacidemia", "Lactic Acidosis", "acidosis lactic", "Acidosis lactic", "lactic acidemia", "Lactic acidosis", "Lactic acidemia", "lactic acidosis", "ACIDOSIS LACTIC", "LACTIC ACIDOSIS", "Lactic acidaemia", "Acidosis, Lactic", "lactic acidaemia", "Lactic acidosis NOS", "Hyperlacticacidemia", "Increased lactate in body", "Lactic acidemia (disorder)", "Lactic acidosis (disorder)", "lactic acidosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lactic acidosis", "shortest_name_length": 12}
{"curie": "MONDO:0003034", "names": ["Mediastinal Angiosarcoma", "mediastinum angiosarcoma", "mediastinal angiosarcoma", "angiosarcoma of mediastinum", "Mediastinal Hemangiosarcoma", "mediastinal hemangiosarcoma", "Angiosarcoma of Mediastinum", "hemangiosarcoma of mediastinum", "Hemangiosarcoma of Mediastinum", "Angiosarcoma of the Mediastinum", "angiosarcoma of the mediastinum", "Hemangiosarcoma of the Mediastinum", "mediastinum angiosarcoma (disease)", "hemangiosarcoma of the mediastinum", "angiosarcoma (disease) of mediastinum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mediastinum angiosarcoma", "shortest_name_length": 24}
{"curie": "UMLS:C0347014", "names": ["Metastases to Nervous System", "Metastasis to nervous system", "Metastases to nervous system", "Nervous system metastases NOS", "Metastasis to the Nervous System", "Metastases to nervous system NOS", "Metastatic nervous system neoplasm", "Cancer metastatic to nervous system", "Metastatic Tumor to the Nervous System", "Metastasis to nervous system (diagnosis)", "Metastatic Neoplasm to the Nervous System", "secondary malignant neoplasm nervous system", "nervous system neoplasm malignant metastasis", "secondary malignant neoplasm of nervous system", "Secondary malignant neoplasm of nervous system", "Metastatic malignant neoplasm to nervous system", "Secondary Malignant Tumor to the Nervous System", "Metastatic malignant neoplasm of nervous system", "Secondary Malignant Neoplasm to the Nervous System", "Secondary malignant neoplasm of nervous system, NOS", "Metastatic Malignant Neoplasm to the Nervous System", "Metastatic Malignant Neoplasm in the Nervous System", "Metastatic malignant neoplasm to nervous system, NOS", "secondary malignant neoplasm of nervous system (diagnosis)", "Metastatic malignant neoplasm to nervous system (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to nervous system", "shortest_name_length": 28}
{"curie": "MONDO:0015790", "names": ["CDI", "central diabetes insipidus", "neurogenic diabetes insipidus", "diabetes insipidus neurogenic", "diabetes insipidus cranial type", "diabetes insipidus neurohypophyseal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central diabetes insipidus", "shortest_name_length": 3}
{"curie": "MONDO:0035759", "names": ["factor V atlanta bleeding disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "factor V atlanta bleeding disorder", "shortest_name_length": 34}
{"curie": "MONDO:0003631", "names": ["Cervical Serous Adenocarcinoma", "cervical serous adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical serous adenocarcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0005039", "names": ["Genital Disorders", "genital disorders", "reproductive disease", "genital system disease", "reproductive system disease", "Reproductive tract disorder", "Reproductive System Disease", "Reproductive System Disorder", "reproductive system disorder", "disorders reproductive system", "disease of reproductive system", "disorders reproductive systems", "Disorder of reproductive system", "Reproductive tract disorder NOS", "disorder of reproductive system", "Disorder of Reproductive System", "reproductive system disease or disorder", "Non-Neoplastic Reproductive System Disease", "disease or disorder of reproductive system", "Disorder of reproductive system (disorder)", "Non-Neoplastic Reproductive System Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "reproductive system disorder", "shortest_name_length": 17}
{"curie": "UMLS:C3273052", "names": ["Bile Duct Papillary Adenocarcinoma", "Bile Duct IPN with an Associated Invasive Carcinoma", "Bile Duct Papillary Neoplasm with an Associated Invasive Carcinoma", "Intraductal Papillary Neoplasm with an Associated Invasive Carcinoma", "Bile Duct Intraductal Papillary Neoplasm with an Associated Invasive Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bile Duct Papillary Neoplasm with an Associated Invasive Carcinoma", "shortest_name_length": 34}
{"curie": "UMLS:C0334037", "names": ["Intestinal metaplasia", "intestinal metaplasia", "Intestinal Metaplasia", "metaplasia intestinal", "Metaplasia, intestinal", "Intestinal metaplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal metaplasia", "shortest_name_length": 21}
{"curie": "UMLS:C0391996", "names": ["liver atrophy", "Atrophy liver", "ATROPHY LIVER", "Liver atrophy", "atrophy liver", "atrophy; liver", "liver; atrophy", "Hepatic atrophy", "Atrophy of liver", "Hepatic atrophy, NOS", "Atrophy of liver, NOS", "Atrophy of liver (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atrophy of liver", "shortest_name_length": 13}
{"curie": "MONDO:0001261", "names": ["mobitz ii", "Mobitz II", "Möbitz II", "non-wenckebach", "type 2 2nd degree AV block", "Type 2 2nd degree AV Block", "AV block-2nd degree-type 2", "Second degree AV heart block", "type 2 second degree AV block", "Type 2 Second Degree AV Block", "type II second degree AV block", "Type II Second Degree AV Block", "AV BLOCK SECOND DEGREE MOBITZ II", "Mobitz II atrioventricular block", "Mobitz type 2 atrioventricular block", "Möbitz Type II Second Degree AV Block", "AV block second degree Möbitz type II", "AV Block Second Degree Mobitz Type II", "AV block second degree Mobitz type II", "Mobitz type II second degree AV block", "Möbitz type II second degree AV block", "Mobitz Type II Second Degree AV Block", "Mobitz type II atrioventricular block", "AV Block Second Degree Möbitz Type II", "Second degree AV block, Mobitz type II", "MOBITZ TYPE 2 SECOND DEGREE HEART BLOCK", "Mobitz (type) II atrioventricular block", "second degree A-V block, Mobitz type II", "Mobitz type II atrioventricular heart block", "type II second degree atrioventricular block", "Type II Second Degree Atrioventricular Block", "Incomplete atrioventricular block, Mobitz II", "Second degree AV heart block - Mobitz type 2", "Type II second degree atrioventricular block", "Mobitz type II atrioventricular block (disorder)", "Mobitz type II incomplete atrioventricular block", "Mobitz type II atrioventricular block (diagnosis)", "Incomplete atrioventricular block, Mobitz type II", "Mobitz type 2 second degree atrioventricular block", "Second Degree Atrioventricular Block Möbitz Type II", "second degree atrioventricular block Möbitz type II", "Second Degree Atrioventricular Block Mobitz Type II", "second degree atrioventricular block Mobitz type II", "Incomplete atrioventricular block, second degree, Mobitz II", "Second degree Mobitz type II incomplete atrioventricular block", "Incomplete atrioventricular block, second degree, Mobitz type II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mobitz type II atrioventricular block", "shortest_name_length": 9}
{"curie": "UMLS:C5557385", "names": ["Vulvar Rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Rhabdomyosarcoma", "shortest_name_length": 23}
{"curie": "MONDO:0027772", "names": ["Lung Colloid Adenocarcinoma", "lung colloid adenocarcinoma", "mucinous lung adenocarcinoma", "Mucinous adenocarcinoma of lung", "mucinous adenocarcinoma of lung", "lung mucinous cystadenocarcinoma", "Lung Mucinous Cystadenocarcinoma", "Mucinous adenocarcinoma of lung (disorder)", "mucinous adenocarcinoma of lung (diagnosis)", "Mucinous cystic tumor of borderline malignancy", "lung mucinous cystic tumor of borderline malignancy", "Lung Mucinous Cystic Tumor of Borderline Malignancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung colloid adenocarcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0100453", "names": ["LCA", "CRB", "RCD2", "LCA1", "CORD6", "cone-rod dystrophy 6", "retinal cone dystrophy 2", "cone-rod dystrophy type 6", "GUCY2D cone-rod dystrophy", "Leber congenital amaurosis 1", "recessive GUCY2D retinopathy", "retinal blindness, congenital", "amaurosis congenita of Leber I", "amaurosis congenita of Leber 1", "Leber congenital amaurosis type 1", "GUCY2D Leber congenital amaurosis", "amaurosis congenita of Leber, type 1", "GUCY2D-related recessive retinopathy", "night blindness, congenital stationary, type 1I", "cone-rod dystrophy caused by mutation in GUCY2D", "Leber congenital amaurosis caused by mutation in GUCY2D"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "GUCY2D-related recessive retinopathy", "shortest_name_length": 3}
{"curie": "MONDO:0002326", "names": ["alcohol-induced mental disorder", "Other alcohol-induced mental disorders", "Other specified alcohol-induced mental disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alcohol-induced mental disorder", "shortest_name_length": 31}
{"curie": "UMLS:C4683665", "names": ["Extranodal Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue by Ann Arbor Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extranodal Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue by Ann Arbor Stage", "shortest_name_length": 89}
{"curie": "MONDO:0019733", "names": ["AFib amyloidosis", "fibrinogen A alpha-chain amyloidosis", "hereditary renal amyloidosis due to fibrinogen A alpha-chain variant", "familial amyloid nephropathy due to fibrinogen A alpha-chain variant", "hereditary amyloid nephropathy due to fibrinogen A alpha-chain variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AFib amyloidosis", "shortest_name_length": 16}
{"curie": "UMLS:C0018674", "names": ["head injury", "Injury;head", "Head trauma", "Injury-head", "head trauma", "Head Trauma", "Head Injury", "HEAD TRAUMA", "HEAD INJURY", "Head injury", "head; injury", "head traumas", "Injury, Head", "Head Traumas", "injury; head", "Trauma, Head", "Traumas, Head", "head injuries", "Head Injuries", "Injury of Head", "Injury of head", "Injuries, Head", "Head injury NOS", "HI - Head injury", "Head injury, NOS", "Injury of head, NOS", "injuries to the head", "Injuries to the head", "craniocerebral trauma", "Craniocerebral Trauma", "Craniocerebral Injury", "Craniocerebral injury", "craniocerebral injury", "Injury of head region", "Injury, Craniocerebral", "Trauma, Craniocerebral", "Craniocerebral Traumas", "Traumas, Craniocerebral", "Craniocerebral Injuries", "head trauma (diagnosis)", "head injury (diagnosis)", "Cranioencephalic trauma", "Injuries, Craniocerebral", "Head injury, unspecified", "Injury of head (disorder)", "Unspecified injury of head", "Injuries to the head (S00-S09)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Craniocerebral Trauma", "shortest_name_length": 11}
{"curie": "MONDO:0014451", "names": ["FSGS7", "FOCAL SEGMENTAL GLOMERULOSCLEROSIS 7", "focal segmental glomerulosclerosis 7", "glomerulosclerosis, focal segmental, 7", "GLOMERULOSCLEROSIS, FOCAL SEGMENTAL, 7", "PAX2 focal segmental glomerulosclerosis", "focal segmental glomerulosclerosis type 7", "focal segmental glomerulosclerosis caused by mutation in PAX2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal segmental glomerulosclerosis 7", "shortest_name_length": 5}
{"curie": "UMLS:C0152155", "names": ["Threatened labor", "threatened labor", "Labor, threatened", "threatened labour", "Threatened labour", "Labour;threatened"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Threatened labor", "shortest_name_length": 16}
{"curie": "MONDO:0006868", "names": ["BOWEL NEUROGENIC", "neurogenic bowel", "Neurogenic bowel", "Neurogenic Bowel", "neurogenic; bowel", "Bowel, Neurogenic", "bowel; neurogenic", "Neurogenic Bowels", "Bowels, Neurogenic", "Neurogenic bowel (disorder)", "neurogenic bowel (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurogenic bowel", "shortest_name_length": 16}
{"curie": "MONDO:0008179", "names": ["PEPD", "Pexpd", "PEXPD", "familial rectal pain", "Familial rectal pain", "Familial Rectal Pain", "RECTAL PAIN, FAMILIAL", "rectal pain, familial", "Rectal Pain, Familial", "familial rectal syndrome", "paroxysmal extreme pain disorder", "Paroxysmal Extreme Pain Disorder", "Paroxysmal extreme pain disorder", "PAROXYSMAL EXTREME PAIN DISORDER", "Paroxysmal extreme pain disorder (disorder)", "submandibular, ocular and rectal pain with flushing", "Submandibular, ocular and rectal pain with flushing", "Submandibular, Ocular, and Rectal Pain with Flushing", "submandibular, ocular, and rectal pain with flushing", "Pain, Submandibular, Ocular, wnd Rectal, with Flushing", "pain, submandibular, ocular, and rectal, with flushing", "PAIN, SUBMANDIBULAR, OCULAR, AND RECTAL, WITH FLUSHING"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paroxysmal extreme pain disorder", "shortest_name_length": 4}
{"curie": "MONDO:0005110", "names": ["CARDIOMYOPATHY PRIMARY", "cardiomyopathy primary", "Primary Cardiomyopathy", "primary cardiomyopathy", "Cardiomyopathy primary", "Cardiomyopathy;primary", "Primary cardiomyopathy", "Cardiomyopathy, Primary", "primary; cardiomyopathy", "cardiomyopathy; primary", "Idiopathic cardiomegaly", "cardiomegaly; idiopathic", "Primary Cardiomyopathies", "idiopathic; cardiomegaly", "CARDIOMEGALY, IDIOPATHIC", "Idiopathic Cardiomyopathy", "CARDIOMYOPATHY IDIOPATHIC", "Cardiomyopathies, Primary", "idiopathic cardiomyopathy", "Idiopathic cardiomyopathy", "IDIOPATHIC CARDIOMYOPATHY", "Cardiomyopathy primary NOS", "Primary Myocardial Disease", "Cardiomyopathy, idiopathic", "Disease, Primary Myocardial", "Primary Myocardial Diseases", "Myocardial Disease, Primary", "CARDIOMYOPATHY, NONCORONARY", "Diseases, Primary Myocardial", "Myocardial Diseases, Primary", "Primary cardiomyopathy (disorder)", "Primary idiopathic cardiomyopathy", "myocardium; disease, primary (idiopathic)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic cardiomyopathy", "shortest_name_length": 22}
{"curie": "UMLS:C5418759", "names": ["Primary Peritoneal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Peritoneal Adenocarcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0019473", "names": ["ETTL", "EATL", "EATCL", "EATL, type I", "EATL, Type I", "Intestinal T-cell lymphoma", "intestinal T-cell lymphoma", "Enteropathy-type T-cell lymphoma", "Enteropathy-Type T-Cell Lymphoma", "enteropathy-type T-cell lymphoma", "Enteropathy Associated T-Cell Lymphoma", "enteropathy-associated T-cell lymphoma", "Enteropathy Associated T Cell Lymphoma", "Enteropathy associated T-cell lymphoma", "Enteropathy-Associated T-Cell Lymphoma", "enteropathy associated T-cell lymphoma", "Enteropathy-associated T-cell lymphoma", "T Cell Lymphoma, Enteropathy Associated", "Enteropathy-Associated T-Cell Lymphomas", "T-Cell Lymphoma, Enteropathy-Associated", "Lymphoma, T-Cell, Enteropathy-Associated", "Lymphomas, Enteropathy-Associated T-Cell", "T-Cell Lymphomas, Enteropathy-Associated", "Enteropathy type intestinal T-cell lymphoma", "EATL - enteropathy-associated T-cell lymphoma", "Enteropathy-type (intestinal) T-cell lymphoma", "Enteropathy type (intestinal) T-cell lymphoma", "EACTL - Enteropathy-associated T-cell lymphoma", "Enteropathy-Associated T-Cell Lymphoma, Type I", "enteropathy-associated T-cell lymphoma, type I", "digestive malignant lymphoma intestinal T-cell", "Enteropathy-associated T-cell lymphoma (disorder)", "high-grade pleomorphic peripheral T-cell lymphoma", "Enteropathy associated T-cell lymphoma (diagnosis)", "Enteropathy-associated T-cell lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "enteropathy-associated T-cell lymphoma", "shortest_name_length": 4}
{"curie": "MONDO:0007626", "names": ["hereditary fourth cranial nerve palsy", "strabismus from Superior oblique palsy", "Strabismus from Superior Oblique Palsy", "STRABISMUS FROM SUPERIOR OBLIQUE PALSY", "trochlear nerve palsy, familial congenital", "Trochlear Nerve Palsy, Familial Congenital", "TROCHLEAR NERVE PALSY, FAMILIAL CONGENITAL", "Familial congenital palsy of trochlear nerve", "familial congenital palsy of trochlear nerve", "fourth cranial nerve palsy, familial congenital", "FOURTH CRANIAL NERVE PALSY, FAMILIAL CONGENITAL", "superior oblique oculomotor palsy, familial congenital", "Superior Oblique Oculomotor Palsy, Familial Congenital", "SUPERIOR OBLIQUE OCULOMOTOR PALSY, FAMILIAL CONGENITAL", "Familial congenital palsy of trochlear nerve (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial congenital palsy of trochlear nerve", "shortest_name_length": 37}
{"curie": "UMLS:C5206445", "names": ["Stage IIA1 Cervical Cancer FIGO 2018", "Stage IIA1 Cervical Carcinoma FIGO 2018"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA1 Cervical Cancer FIGO 2018", "shortest_name_length": 36}
{"curie": "UMLS:C1444214", "names": ["Atresia", "ATRESIA", "Atretic", "Impatent structure", "Impatent structure (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Impatent structure", "shortest_name_length": 7}
{"curie": "UMLS:C5418982", "names": ["Central Nervous System Involvement in Relapsed B Acute Lymphoblastic Leukemia", "Central Nervous System Involvement in Recurrent B Acute Lymphoblastic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Involvement in Recurrent B Acute Lymphoblastic Leukemia", "shortest_name_length": 77}
{"curie": "MONDO:0004759", "names": ["Zoophilia", "zoophilia", "bestiality", "Bestiality", "zoophilia (diagnosis)", "Bestiality (disorder)", "Bestiality (Zoophilia)", "bestiality (Zoophilia)", "deviation; sexual, bestiality", "sexual; deviation, bestiality"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bestiality", "shortest_name_length": 9}
{"curie": "UMLS:C4724853", "names": ["Refractory Head and Neck Squamous Cell Cancer", "Refractory Head and Neck Squamous Cell Carcinoma", "Refractory Squamous Cell Carcinoma of the Head and Neck"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Head and Neck Squamous Cell Carcinoma", "shortest_name_length": 45}
{"curie": "MONDO:0014056", "names": ["CMM9", "melanoma, cutaneous malignant, 9", "susceptibility to cutaneous malignant melanoma 9", "melanoma, cutaneous malignant, susceptibility to, 9", "MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 9", "melanoma, cutaneous malignant, susceptibility to, type 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melanoma, cutaneous malignant, susceptibility to, 9", "shortest_name_length": 4}
{"curie": "UMLS:C5442486", "names": ["Immune-mediated lung disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immune-mediated lung disease", "shortest_name_length": 28}
{"curie": "UMLS:C4551869", "names": ["Stage I Nasopharyngeal Carcinoma", "Stage I Nasopharyngeal Throat Cancer", "Stage I Nasopharyngeal Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Nasopharyngeal Carcinoma AJCC v7", "shortest_name_length": 32}
{"curie": "MONDO:0006344", "names": ["yolk sac tumor", "ovary yolk sac tumor", "Ovarian Yolk Sac tumor", "ovarian yolk sac tumor", "Ovarian Yolk Sac Tumor", "Ovarian Yolk Sac tumour", "Yolk Sac Tumor of Ovary", "Yolk sac tumor of ovary", "yolk sac tumor of ovary", "yolk Sac tumor of ovary", "Yolk sac tumour of ovary", "ovarian yolk Sac neoplasm", "Ovarian Yolk Sac Neoplasm", "Yolk Sac Neoplasm of Ovary", "yolk Sac neoplasm of ovary", "yolk Sac tumor of the ovary", "Yolk Sac Tumor of the Ovary", "Yolk Sac Neoplasm of the Ovary", "Ovarian Endodermal Sinus Tumor", "yolk Sac neoplasm of the ovary", "ovarian endodermal sinus tumor", "Endodermal Sinus Tumor of Ovary", "ovarian endodermal sinus tumour", "endodermal sinus tumor of ovary", "Endodermal sinus tumor of ovary", "Ovarian germ cell yolk sac tumor", "Endodermal sinus tumour of ovary", "ovarian endodermal sinus neoplasm", "Ovarian Endodermal Sinus Neoplasm", "Ovarian germ cell yolk sac tumour", "Endodermal Sinus Neoplasm of Ovary", "endodermal sinus neoplasm of ovary", "endodermal sinus tumor of the ovary", "yolk sac tumor of ovary (diagnosis)", "Endodermal Sinus Tumor of the Ovary", "endodermal sinus neoplasm of the ovary", "Endodermal Sinus Neoplasm of the Ovary", "Ovarian Germ Cell Endodermal Sinus Tumor", "ovarian germ cell endodermal sinus tumor", "Ovarian germ cell endodermal sinus tumor", "Ovarian germ cell endodermal sinus tumour", "germ cell endodermal sinus tumor of ovary", "Germ Cell Endodermal Sinus Tumor of Ovary", "Endodermal sinus tumor of ovary (disorder)", "Ovarian Germ Cell Endodermal Sinus Neoplasm", "ovarian germ cell endodermal sinus neoplasm", "Endodermal sinus tumor of ovary (diagnosis)", "germ cell endodermal sinus neoplasm of ovary", "Germ Cell Endodermal Sinus Neoplasm of Ovary", "germ cell endodermal sinus tumor of the ovary", "Germ Cell Endodermal Sinus Tumor of the Ovary", "germ cell endodermal sinus neoplasm of the ovary", "Germ Cell Endodermal Sinus Neoplasm of the Ovary", "ovarian neoplasm malignant germ cell tumor endodermal sinus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian yolk sac tumor", "shortest_name_length": 14}
{"curie": "UMLS:C0597457", "names": ["Skeletal injury", "skeletal injury", "injuries skeletal", "Skeletal injury NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skeletal injury", "shortest_name_length": 15}
{"curie": "MONDO:0700171", "names": ["Horse Melanoma", "horse melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "horse melanoma", "shortest_name_length": 14}
{"curie": "MONDO:0002852", "names": ["Mediastinal Sarcoma", "mediastinum sarcoma", "mediastinal sarcoma", "Sarcoma of Mediastinum", "sarcoma of mediastinum", "Sarcoma of the Mediastinum", "sarcoma of the mediastinum", "sarcoma of mediastinum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mediastinum sarcoma", "shortest_name_length": 19}
{"curie": "MONDO:0011401", "names": ["AD15", "Alzheimer Disease 15", "Alzheimer disease 15", "ALZHEIMER DISEASE 15", "Alzheimer disease-15", "Alzheimer's disease 15", "Alzheimer's disease type 15", "Alzheimer's disease 15, late onset", "Alzheimer's disease without Tau pathology", "ALZHEIMER DISEASE WITHOUT NEUROFIBRILLARY TANGLES", "Alzheimer disease without neurofibrillary tangles", "Alzheimer Disease Without Neurofibrillary Tangles", "Alzheimer's disease without neurofibrillary tangles", "Alzheimer's disease without Neurofibrillary tangles"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alzheimer disease without neurofibrillary tangles", "shortest_name_length": 4}
{"curie": "MONDO:0014350", "names": ["SCKL8", "SECKEL SYNDROME 8", "Seckel syndrome 8", "DNA2 Seckel syndrome", "Seckel syndrome type 8", "Seckel syndrome caused by mutation in DNA2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Seckel syndrome 8", "shortest_name_length": 5}
{"curie": "MONDO:0019042", "names": ["MCAHS", "multiple congenital anomalies/dysmorphic syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple congenital anomalies/dysmorphic syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0015357", "names": ["secondary hypoparathyroidism due to impaired parathormon secretion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary hypoparathyroidism due to impaired parathormon secretion", "shortest_name_length": 66}
{"curie": "UMLS:C1707332", "names": ["Cellular Myxoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cellular Myxoma", "shortest_name_length": 15}
{"curie": "OMIM:210750", "names": ["Shep6", "SHEP6", "Skin-Hair-Eye Pigmentation, Variation In, 6", "SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 6", "Skin-Hair-Eye Pigmentation 6, Blue-Green Eyes", "SKIN/HAIR/EYE PIGMENTATION 6, BLUE/GREEN EYES", "Skin-Hair-Eye Pigmentation 6, Blond-Brown Hair", "SKIN/HAIR/EYE PIGMENTATION 6, BLOND/BROWN HAIR", "SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 6 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 5}
{"curie": "UMLS:C0025061", "names": ["mediastinum disease", "Mediastinal Disease", "Mediastinal disease", "mediastinal disease", "Mediastinal Disorder", "Mediastinal disorder", "Mediastinal Diseases", "Disease, Mediastinal", "Mediastinal Disorders", "Mediastinal disorders", "Mediastinum--Diseases", "Diseases, Mediastinal", "mediastinum; disorder", "DISEASE OF MEDIASTINUM", "Disorder of mediastinum", "Mediastinal disorder NOS", "DISEASES OF THE MEDIASTINUM", "Disease of mediastinum, NOS", "Mediastinal disorders (diagnosis)", "Disorder of mediastinum (disorder)", "disease (or disorder); mediastinum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mediastinal Diseases", "shortest_name_length": 19}
{"curie": "UMLS:C4316808", "names": ["childhood cerebral ependymoma", "Childhood Cerebral Ependymoma, NOS", "Childhood Cerebral Ependymoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Cerebral Ependymoma, Not Otherwise Specified", "shortest_name_length": 29}
{"curie": "UMLS:C4721659", "names": ["Stage III Ovarian Teratoma", "Stage III Ovarian Teratoma AJCC v7", "Stage III Ovarian Teratoma AJCC v6", "Ovarian Germ Cell Teratoma Stage III", "Stage III Ovarian Germ Cell Teratoma", "Ovarian Germ Cell Teratoma, Stage III", "Stage III Ovarian Teratoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Ovarian Teratoma AJCC v6 and v7", "shortest_name_length": 26}
{"curie": "UMLS:C4528623", "names": ["Stage IIIC Vulvar Cancer", "Stage IIIC Vulvar Cancer AJCC v8", "Stage IIIC Vulvar Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Vulvar Cancer AJCC v8", "shortest_name_length": 24}
{"curie": "UMLS:C0015734", "names": ["Scybala", "Scybalum", "Coprostasis", "COPROSTASIS", "coprostasis", "impacted stool", "STOOL IMPACTED", "Impacted feces", "impacted feces", "feces impacted", "Impacted faeces", "Impaction fecal", "Fecal impaction", "FECAL IMPACTION", "FECES, IMPACTED", "Stool impaction", "IMPACTION FECAL", "fecal impaction", "impacted stools", "Fecal Impaction", "impacted faeces", "fecal impactions", "faecal impaction", "Impaction, Fecal", "Feces - impacted", "FAECAL IMPACTION", "fecal; impaction", "Faecal impaction", "impaction; fecal", "Impaction faecal", "Faecal Impaction", "Impaction, fecal", "Faeces - impacted", "Fecal impaction NOS", "impacted with feces", "impacted with stool", "RNDx fecal impaction", "Impacted stool in rectum", "Fecal impaction (disorder)", "fecal impaction (diagnosis)", "fecal impaction was discovered", "RNDx fecal impaction (diagnosis)", "fecal impaction (physical finding)", "Fecal impaction (excl obstruction)", "Faecal impaction (excl obstruction)", "Fecal impaction (excluding obstruction)", "Fecal impaction (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fecal Impaction", "shortest_name_length": 7}
{"curie": "UMLS:C0919986", "names": ["Edema infusion site", "Infusion site edema", "Infusion site oedema", "Oedema infusion site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infusion site edema", "shortest_name_length": 19}
{"curie": "UMLS:C2749602", "names": ["AUTOIMMUNE POLYENDOCRINOPATHY SYNDROME, TYPE I, WITH REVERSIBLE METAPHYSEAL DYSPLASIA", "Autoimmune Polyendocrinopathy Syndrome, Type I, With Reversible Metaphyseal Dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AUTOIMMUNE POLYENDOCRINOPATHY SYNDROME, TYPE I, WITH REVERSIBLE METAPHYSEAL DYSPLASIA", "shortest_name_length": 85}
{"curie": "UMLS:C5669877", "names": ["Diffuse Midline Glioma, H3 K27-Altered"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse Midline Glioma, H3 K27-Altered", "shortest_name_length": 38}
{"curie": "UMLS:C4553667", "names": ["Stage IIIB Ovarian Cancer", "Stage IIIB Ovarian Cancer AJCC v8", "Stage IIIB Ovarian Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Ovarian Cancer AJCC v8", "shortest_name_length": 25}
{"curie": "MONDO:0003973", "names": ["tubular variant testicular seminoma", "testicular seminoma, tubular variant", "Testicular Seminoma, Tubular Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tubular variant testicular seminoma", "shortest_name_length": 35}
{"curie": "UMLS:C4086178", "names": ["Childhood Papillary Thyroid Carcinoma", "Childhood Thyroid Gland Papillary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Thyroid Gland Papillary Carcinoma", "shortest_name_length": 37}
{"curie": "UMLS:C4721421", "names": ["breast cancer stage iii", "stage III breast cancer", "Breast Cancer Stage III", "Breast cancer stage III", "stage iii breast cancer", "breast cancer, stage III", "Breast cancer NOS stage III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast cancer stage III", "shortest_name_length": 23}
{"curie": "MONDO:0004995", "names": ["CVD", "CVD, NOS", "CVS disease", "CV disorders", "circulatory disorder", "circulation disorder", "circulatory; disorder", "circulation disorders", "circulatory disorders", "Circulatory Disorders", "Cardiovascular_Disease", "Disease;cardiovascular", "CARDIOVASCULAR DISEASE", "cardiovascular disease", "Cardiovascular disease", "Cardiovascular Disease", "Cardiovascular disorder", "Cardiovascular Diseases", "cardiovascular disorder", "cardiovascular diseases", "Disease, Cardiovascular", "Cardiovascular Disorder", "CARDIOVASCULAR DISORDER", "CARDIOVASCULAR DISORDERS", "cardiovascular; disorder", "cardiovascular disorders", "Cardiovascular Disorders", "Circulation, Disorders of", "circulatory system disease", "circulatory disease system", "disease circulatory system", "Cardiovascular abnormality", "CARDIOVASCULAR ABNORMALITY", "Cardiovascular Abnormality", "DISORDER CIRCULATORY SYSTEM", "circulatory diseases system", "Cardiovascular disease, NOS", "circulatory disorder system", "Cardiovascular disorder NOS", "Abnormality, Cardiovascular", "circulatory system diseases", "circulatory system disorder", "Disorder circulatory system", "circulatory disorders system", "cardiovascular disease (CVD)", "cardiovascular abnormalities", "abnormalities cardiovascular", "Cardiovascular Abnormalities", "CVD - cardiovascular disease", "Cardiovascular Disorder, NOS", "Cardiovascular Disease (CVD)", "Cardiovascular disorder, NOS", "Abnormalities, Cardiovascular", "cardiovascular system disease", "CARDIOVASCULAR DISORDER (NOS)", "DISORDER CARDIOVASCULAR (NOS)", "Cardiovascular system disease", "Disorder of circulatory system", "cardiovascular system diseases", "anomaly; cardiovascular system", "cardiovascular system; anomaly", "Cardiovascular system--Diseases", "deformity; cardiovascular system", "cardiovascular system; deformity", "disease of cardiovascular system", "CIRCULATORY SYSTEM DISORDER (NOS)", "Disorder of cardiovascular system", "Disorder of Cardiovascular System", "CARDIOVASCULAR DISORDERS, GENERAL", "disorder of cardiovascular system", "Diseases of the circulatory system", "disease (or disorder); circulatory", "DISEASES OF THE CIRCULATORY SYSTEM", "Disorder of the circulatory system", "Cardiovascular disease, unspecified", "Disorder of circulatory system, NOS", "Cardiovascular system--Abnormalities", "cardiovascular disorders (diagnosis)", "DISEASES OF THE CARDIOVASCULAR SYSTEM", "disease (or disorder); cardiovascular", "Disease of cardiovascular system, NOS", "Unspecified circulatory system disorder", "CARDIOVASCULAR DISORDERS: GENERAL TERMS", "Abnormality of the cardiovascular system", "cardiovascular system disease or disorder", "Unspecified disorder of circulatory system", "CVS disease - cardiovascular system disease", "Diseases of the circulatory system (I00-I99)", "Disorder of cardiovascular system (disorder)", "disease or disorder of cardiovascular system", "Disease or syndrome of cardiovascular system", "disease of subdivision of hemolymphoid system", "Diseases and Syndromes of Cardiovascular System", "DISEASES AFFECTING THE ENTIRE CARDIOVASCULAR SYSTEM", "General Cardiovascular System Diseases and Syndromes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiovascular disorder", "shortest_name_length": 3}
{"curie": "UMLS:C0280169", "names": ["Stage IV", "Stage IV Grade 1 Follicular Lymphoma", "Grade I Follicular Lymphoma Stage IV", "stage IV grade 1 follicular lymphoma", "Grade I Stage IV Follicular Lymphoma", "Metastatic Grade I Follicular Lymphoma", "Ann Arbor Stage IV Grade 1 Follicular Lymphoma", "Follicular Small Cleaved Cell Lymphoma Stage IV", "Stage IV Follicular Small Cleaved Cell Lymphoma", "follicular small cleaved cell lymphoma, stage IV", "metastatic follicular small cleaved cell lymphoma", "follicular small cleaved cell lymphoma, metastatic", "stage IV grade I follicular small cleaved cell lymphoma", "Grade I Follicular Small Cleaved Cell Lymphoma Stage IV", "Grade I Stage IV Follicular Small Cleaved Cell Lymphoma", "Metastatic Grade I Follicular Small Cleaved Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage IV Grade 1 Follicular Lymphoma", "shortest_name_length": 8}
{"curie": "UMLS:C4288052", "names": ["Uterine Corpus Carcinoid Tumor", "Uterine Corpus Neuroendocrine Tumor G1", "Uterine Corpus Neuroendocrine Tumor Grade 1", "Uterine Corpus Well Differentiated Neuroendocrine Tumor, Grade 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Corpus Neuroendocrine Tumor G1", "shortest_name_length": 30}
{"curie": "MONDO:0003812", "names": ["ovary endometrioid tumor", "ovarian endometrial cancer", "Ovarian Endometrioid Tumor", "endometrioid tumor of ovary", "Ovarian Endometrioid Neoplasm", "ovarian endometrioid neoplasm", "Endometrioid Neoplasm of Ovary", "endometrioid neoplasm of Ovary", "endometrioid neoplasm of ovary", "Endometrioid Neoplasm of the Ovary", "Malignant Ovarian Endometrioid Tumor", "malignant ovarian endometrioid tumor", "ovary female reproductive endometrioid cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian endometrial cancer", "shortest_name_length": 24}
{"curie": "UMLS:C4329965", "names": ["Factor III Inactivation", "Factor III Inhibitor Present", "Tissue Factor Inhibitor Present"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Factor III Inactivation", "shortest_name_length": 23}
{"curie": "UMLS:C5208352", "names": ["Cutaneous Langerhans cell histiocytosis", "Cutaneous Langerhans Cell Histiocytosis", "Cutaneous Langerhans cell histiocytosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous Langerhans cell histiocytosis", "shortest_name_length": 39}
{"curie": "MONDO:0018924", "names": ["MCOPS1", "Lenz dysplasia", "MAA (formerly)", "Lenz microphthalmia", "microphthalmia Lenz type", "microphthalmia, Lenz type", "microphthalmia syndromic 1", "Lenz microphthamia syndrome", "syndromic microphthalmia type 1", "microphthalmia or anophthalmos with associated anomalies (formerly)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microphthalmia, Lenz type", "shortest_name_length": 6}
{"curie": "UMLS:C1299539", "names": ["Scrotal infection", "infection scrotum", "scrotal infection", "scrotum infection", "Scrotal Infection", "infection; scrotum", "infections scrotal", "infections scrotum", "scrotum; infection", "infection of scrotum", "Infection of scrotum", "Scrotal infection NOS", "Scrotal infection (diagnosis)", "Infection of scrotum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Scrotal Infection", "shortest_name_length": 17}
{"curie": "MONDO:0003003", "names": ["cervical alveolar soft part sarcoma", "Cervical Alveolar Soft Part Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical alveolar soft part sarcoma", "shortest_name_length": 35}
{"curie": "MONDO:0800064", "names": ["osteogenesis imperfecta and a reduction of bone mineral density."], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteogenesis imperfecta and a reduction of bone mineral density.", "shortest_name_length": 64}
{"curie": "MONDO:0009572", "names": ["FMF", "FMF autosomal recessive", "polyserositis, recurrent", "familial Mediterranean fever", "familial MEDITERRANEAN FEVER", "familial Mediterranean fever, AR", "polyserositis, familial paroxysmal", "FMF autosomal recessive (diagnosis)", "familial Mediterranean fever autosomal recessive", "autosomal recessive familial Mediterranean fever", "Familial Mediterranean Fever, Autosomal Recessive", "familial Mediterranean fever, autosomal recessive", "FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive familial Mediterranean fever", "shortest_name_length": 3}
{"curie": "UMLS:C0751917", "names": ["Transitional PMD", "Transitional Pelizaeus-Merzbacher Disease", "Transitional Pelizaeus Merzbacher Disease", "Pelizaeus-Merzbacher Disease, Transitional", "Pelizaeus Merzbacher Disease, Transitional", "Pelizaeus-Merzbacher disease, transitional form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pelizaeus-Merzbacher Disease, Transitional", "shortest_name_length": 16}
{"curie": "UMLS:C0524679", "names": ["neuropapillitis", "Neuropapillitis", "Neuropapillitides", "Anterior Optic Neuritis", "Neuritis, Anterior Optic", "Optic Neuritis, Anterior", "Anterior Optic Neuritides", "Optic Neuritides, Anterior", "Neuritides, Anterior Optic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neuropapillitis", "shortest_name_length": 15}
{"curie": "MONDO:0004043", "names": ["ureter inverted papilloma", "Ureter Inverted Papilloma", "ureteral inverted papilloma", "ureteral Inverted papilloma", "Ureteral Inverted Papilloma", "inverted papilloma of ureter", "Inverted Papilloma of Ureter", "Inverted Papilloma of the Ureter", "inverted papilloma of the ureter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ureter inverted papilloma", "shortest_name_length": 25}
{"curie": "MONDO:0011584", "names": ["FAD1", "Fad1", "FANCD1", "Fanconi anemia complementation group D1", "Fanconi Anemia, Complementation Group D1", "Fanconi anemia, complementation group D1", "FANCONI ANEMIA, COMPLEMENTATION GROUP D1", "Fanconi anemia complementation group D1 (diagnosis)", "Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutation", "inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations", "Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations", "Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fanconi anemia complementation group D1", "shortest_name_length": 4}
{"curie": "MONDO:0012524", "names": ["FHHA1B", "Cmo 2 deficiency", "CMO II DEFICIENCY", "CMO II deficiency", "18-oxidase deficiency", "18-OXIDASE DEFICIENCY", "aldosterone deficiency 2", "ALDOSTERONE DEFICIENCY II", "STEROID 18-OXIDASE DEFICIENCY", "steroid 18-oxidase deficiency", "hyperreninemic hypoaldosteronism, familial, 1", "HYPERRENINEMIC HYPOALDOSTERONISM, FAMILIAL, 1", "corticosterone methyloxidase type 2 deficiency", "CORTICOSTERONE METHYLOXIDASE TYPE II DEFICIENCY", "corticosterone methyloxidase type II deficiency", "Corticosterone Methyl Oxidase Type II Deficiency", "Corticosterone methyl oxidase type II deficiency", "18-Hydroxycorticosterone dehydrogenase deficiency", "hypoaldosteronism, congenital, due to CMO II deficiency", "aldosterone deficiency due to deficiency of steroid 18-oxidase", "ALDOSTERONE DEFICIENCY DUE TO DEFICIENCY OF STEROID 18-OXIDASE", "Aldosterone deficiency due to 18-hydroxysteroid dehydrogenase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corticosterone methyloxidase type 2 deficiency", "shortest_name_length": 6}
{"curie": "MONDO:0009680", "names": ["Bassoe syndrome", "Familial congenital muscular dystrophy with gonadal dysgenesis", "familial congenital muscular dystrophy with gonadal dysgenesis", "Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome", "congenital muscular dystrophy-infantile cataract-hypogonadism syndrome", "Muscular Dystrophy, Congenital, with Infantile Cataract and Hypogonadism", "muscular dystrophy, congenital, with infantile cataract and hypogonadism", "Muscular dystrophy, congenital, infantile with cataract and hypogonadism", "muscular dystrophy, congenital, infantile with cataract and hypogonadism", "MUSCULAR DYSTROPHY, CONGENITAL, WITH INFANTILE CATARACT AND HYPOGONADISM", "Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome", "benign muscular dystrophy with hypergonadotrophic hypogonadism and congenital cataract", "Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital muscular dystrophy-infantile cataract-hypogonadism syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0010125", "names": ["upper limb defect-eye and ear abnormalities syndrome", "thumb, hypoplastic, with choroid coloboma, poorly developed antihelix, and deafness", "Thumb, Hypoplastic, with Choroid Coloboma, Poorly Developed Antihelix, and Deafness", "THUMB, HYPOPLASTIC, WITH CHOROID COLOBOMA, POORLY DEVELOPED ANTIHELIX, AND DEAFNESS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "upper limb defect-eye and ear abnormalities syndrome", "shortest_name_length": 52}
{"curie": "MONDO:0007034", "names": ["AOS", "Type 2 aplasia cutis", "adam oliver syndrome", "adam oliver syndromes", "adams oliver syndrome", "Adams-Oliver syndrome", "syndrome adams-oliver", "adams-oliver syndrome", "Adams Oliver syndrome", "limb scalp and skull defects", "limb, scalp and skull defects", "Limb, scalp and skull defects", "Adams-Oliver syndrome (disorder)", "congenital scalp defects with distal limb anomalies", "Congenital scalp defects with distal limb anomalies", "congenital scalp defects with distal limb reduction anomalies", "Congenital scalp defects with distal limb reduction anomalies", "Congenital absence of skin on scalp with limb-reduction anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adams-Oliver syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C3897238", "names": ["Untreated Anaplastic Oligoastrocytoma", "untreated childhood anaplastic oligoastrocytoma", "Untreated Childhood Anaplastic Oligoastrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Untreated Childhood Anaplastic Oligoastrocytoma", "shortest_name_length": 37}
{"curie": "MONDO:0100417", "names": ["AML, WT1 mutation", "AML, WT1 gene mutation", "AML, GUD Gene Mutation", "AML, WAGR Gene Mutation", "AML, WT33 Gene Mutation", "AML, WIT-2 Gene Mutation", "AML, Wilms Tumor 1 Gene Mutation", "acute myeloid leukemia, WT1 gene mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, WT1 gene mutation", "shortest_name_length": 17}
{"curie": "MONDO:0015129", "names": ["CPAI", "adrenalitis", "ADDISON DISEASE", "Addison Disease", "Addison disease", "addison disease", "Hypocortisolism", "adrenal aplasia", "Addisons disease", "Disease;Addisons", "Addisons Disease", "Disease, Addison", "syndrome; Addison", "DISEASE ADDISON'S", "Addison's disease", "Disease Addison's", "addison's disease", "ADDISON'S DISEASE", "Addison's Disease", "adrenal hypoplasia", "Addison's disease NOS", "primary hypoadrenalism", "Autoimmune Adrenalitis", "autoimmune adrenalitis", "Addison's disease, NOS", "Primary Hypoadrenalism", "Primary hypoadrenalism", "Autoimmune adrenalitis", "adrenalitis; autoimmune", "autoimmune; adrenalitis", "Classic Addison disease", "Hypoadrenalism, Primary", "Primary Addison disease", "Hypoadrenalisms, Primary", "classic Addison's disease", "primary Addison's disease", "adrenal gland hypofunction", "autoimmune Addison disease", "Primary adrenal deficiency", "Autoimmune adrenal atrophy", "Autoimmune Addison disease", "primary; hypoadrenocorticism", "Addison; disease or syndrome", "Addison's disease (disorder)", "hypoadrenocorticism familial", "hypoadrenocorticism; primary", "Autoimmune Addison's disease", "autoimmune addison's disease", "Autoimmune Addison's Disease", "Familial Hypoadrenocorticism", "Adrenocortical insufficiency", "Adrenal atrophy (autoimmune)", "Primary adrenal insufficiency", "Familial Hypoadrenocorticisms", "Hypoadrenocorticism, Familial", "primary adrenal insufficiency", "Hypoadrenocorticism, familial", "HYPOADRENOCORTICISM, FAMILIAL", "Primary Adrenal Insufficiency", "hypoadrenocorticism, familial", "Primary adrenocortical failure", "Adrenal Insufficiency, Primary", "Hypoadrenocorticisms, Familial", "insufficiency; adrenal, primary", "adrenal; insufficiency, primary", "suprarenal; insufficiency, primary", "insufficiency; suprarenal, primary", "corticoadrenal; deficiency, primary", "Addison disease due to autoimmunity", "adrenal cortex; deficiency, primary", "deficiency; corticoadrenal, primary", "deficiency; adrenocortical, primary", "Primary adrenocortical insufficiency", "primary adrenocortical insufficiency", "Primary Adrenocortical Insufficiency", "Chronic adrenocorticoid insufficiency", "Addison's disease due to autoimmunity", "Insufficiency, Primary Adrenocortical", "chronic primary adrenal insufficiency", "Chronic Primary Adrenal Insufficiency", "Adrenocortical Insufficiency, Primary", "adrenal cortex; hypofunction, primary", "chronic adrenocorticoid insufficiency", "Chronic primary adrenal insufficiency", "Primary Adrenocortical Insufficiencies", "primary adrenal insufficiency, chronic", "Adrenal insufficiency (Addison disease)", "Adrenocortical Insufficiencies, Primary", "Insufficiencies, Primary Adrenocortical", "Autoimmune Primary Adrenal Insufficiency", "autoimmune primary adrenal insufficiency", "primary adrenal insufficiency (diagnosis)", "ADRENAL INSUFFICIENCY (ADDISON'S DISEASE)", "ADRENOCORTICAL INSUFFICIENCY, PRIMARY FAILURE", "Addison disease, chronic adrenal insufficiency", "Primary adrenocortical insufficiency (disorder)", "Addison's disease due to autoimmunity (disorder)", "autoimmune primary adrenal insufficiency (diagnosis)", "disease (or disorder); bronzed skin (Addison) (bronze disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic primary adrenal insufficiency", "shortest_name_length": 4}
{"curie": "MONDO:0018420", "names": ["SPG68", "autosomal recessive spastic paraplegia type 68"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive spastic paraplegia type 68", "shortest_name_length": 5}
{"curie": "UMLS:C1881236", "names": ["Interstitial Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Interstitial Disease", "shortest_name_length": 20}
{"curie": "MONDO:0007157", "names": ["AMC", "DA1A", "DA2B4", "distal arthrogryposis type 1A", "arthrogryposis, distal, type 1", "arthrogryposis, distal, type 1A", "arthrogryposis, distal, type 2B4", "ARTHROGRYPOSIS, DISTAL, TYPE 2B4", "arthrogryposis multiplex congenita", "arthrogryposis multiplex congenita, distal, type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis, distal, type 1A", "shortest_name_length": 3}
{"curie": "UMLS:C4687711", "names": ["Progressive Medulloblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Progressive Medulloblastoma", "shortest_name_length": 27}
{"curie": "MONDO:0001223", "names": ["Parathyroid disease", "PARATHYOID DISORDER", "parathyroid disease", "PARATHYROID DISEASE", "Parathyroid Disease", "Parathyroid Diseases", "Parathyroid Disorder", "parathyroid diseases", "PARATHYROID DISORDER", "DISORDER PARATHYROID", "parathyroid disorder", "Disease, Parathyroid", "Parathyroid disorder", "Disorder parathyroid", "parathyroid disorders", "Diseases, Parathyroid", "disorders parathyroid", "Parathyroid Disorders", "Disorder, Parathyroid", "Disorders, Parathyroid", "Dysfunction parathyroid", "parathyroid dysfunction", "DYSFUNCTION PARATHYROID", "Dysfunction;parathyroid", "PARATHYROID DYSFUNCTIUON", "Parathyroid disorder NOS", "Parathyroid Gland Disease", "parathyroid gland disease", "Parathyroid gland disorder", "Parathyroid Gland Diseases", "parathyroid gland disorder", "parathyroid gland diseases", "Parathyroid Gland Disorder", "disorder parathyroid gland", "Parathyroid gland disorders", "Parathyroid Gland Disorders", "parathyroid gland disorders", "disease of parathyroid gland", "Parathyroid glands--Diseases", "disorders glands parathyroid", "disease of parathyroid glands", "Disorder of parathyroid gland", "Disease of parathyroid glands", "disorder of parathyroid gland", "Diseases of Parathyroid Glands", "Disorder of parathyroid glands", "Disorders of parathyroid gland", "DISEASES OF THE PARATHYROID GLANDS", "Disease of parathyroid glands, NOS", "disease (or disorder); parathyroid", "Disorder of parathyroid glands, NOS", "Abnormality of the parathyroid gland", "parathyroid gland disease or disorder", "parathyroid gland disorder (diagnosis)", "disease or disorder of parathyroid gland", "Disorder of parathyroid gland (disorder)", "Unspecified disorder of parathyroid gland", "Disorder of parathyroid gland, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parathyroid gland disorder", "shortest_name_length": 19}
{"curie": "MONDO:0020753", "names": ["coronavirus infectious disease", "Coronavirus infectious disease", "Orthocoronavirinae infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Orthocoronavirinae infectious disease", "shortest_name_length": 30}
{"curie": "MONDO:0023696", "names": ["Marinesco-Sjogren-like syndrome", "Marinesco-Sjogren-like syndrome (MSLS)", "juvenile cataract, cerebellar atrophy, mental retardation, and myopathy", "juvenile cataract-cerebellar atrophy-mental retardation-myopathy syndrome", "juvenile cataract, cerebellar atrophy, intellectual disability, and myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Marinesco-Sjogren-like syndrome", "shortest_name_length": 31}
{"curie": "MONDO:0700159", "names": ["canine acanthomatous epulis", "Canine Acanthomatous Epulis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canine acanthomatous epulis", "shortest_name_length": 27}
{"curie": "UMLS:C3542499", "names": ["ASP Deficiency", "ASPA Deficiency", "ACY2 Deficiency", "Aspartoacylase Deficiency", "Aminoacylase 2 Deficiency", "Deficiency Disease, Aspartoacylase"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aminoacylase 2 Deficiency", "shortest_name_length": 14}
{"curie": "UMLS:C2007068", "names": ["Extrahepatic Bile Duct Carcinosarcoma", "extrahepatic bile duct carcinosarcoma", "carcinosarcoma of extrahepatic bile duct", "carcinosarcoma of the extrahepatic bile duct", "carcinosarcoma of extrahepatic bile duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinosarcoma of extrahepatic bile duct", "shortest_name_length": 37}
{"curie": "UMLS:C4688336", "names": ["Malignant Solid Tumor", "Childhood Malignant Solid Tumor", "Childhood Malignant Solid Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Malignant Solid Neoplasm", "shortest_name_length": 21}
{"curie": "MONDO:0012098", "names": ["SCA20", "Spinocerebellar ataxia 20", "spinocerebellar ataxia 20", "SPINOCEREBELLAR ATAXIA 20", "Spinocerebellar ataxia type 20", "spinocerebellar ataxia type 20", "SCA20 Spinocerebellar ataxia 20", "spinocerebellar ataxia with dysphonia", "Spinocerebellar Ataxia With Dysphonia", "SPINOCEREBELLAR ATAXIA WITH DYSPHONIA", "Spinocerebellar ataxia type 20 (disorder)", "SPINOCEREBELLAR ATAXIA WITH SPASMODIC COUGH", "spinocerebellar ataxia with spasmodic cough", "Spinocerebellar Ataxia With Spasmodic Cough", "chromosome 11q12 duplication syndrome, 260-Kb", "CHROMOSOME 11q12 DUPLICATION SYNDROME, 260-KB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia type 20", "shortest_name_length": 5}
{"curie": "MONDO:0001488", "names": ["Anterior corneal pigmentation", "anterior corneal pigmentation", "anterior corneal pigmentations", "Anterior corneal pigmentations", "Anterior corneal pigmentation (disorder)", "Anterior corneal pigmentations (diagnosis)", "anterior corneal pigmentation (physical finding)", "corneal pigmentations and deposits anterior pigmentation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anterior corneal pigmentation", "shortest_name_length": 29}
{"curie": "UMLS:C5237196", "names": ["Unresectable Digestive System Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Digestive System Neuroendocrine Neoplasm", "shortest_name_length": 53}
{"curie": "EFO:0009459", "names": ["ACPA-positive rheumatoid arthritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ACPA-positive rheumatoid arthritis", "shortest_name_length": 34}
{"curie": "UMLS:C5206583", "names": ["Paratesticular Adenomatoid Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paratesticular Adenomatoid Tumor", "shortest_name_length": 32}
{"curie": "MONDO:0023102", "names": ["Ripperger Aase syndrome", "facio skeletal genital syndrome rippberger type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "facio skeletal genital syndrome rippberger type", "shortest_name_length": 23}
{"curie": "UMLS:C4724966", "names": ["Refractory Undifferentiated Pleomorphic Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Undifferentiated Pleomorphic Sarcoma", "shortest_name_length": 47}
{"curie": "MONDO:0013328", "names": ["RP58", "retinitis pigmentosa 58", "RETINITIS PIGMENTOSA 58", "ZNF513 retinitis pigmentosa", "retinitis pigmentosa type 58", "retinitis pigmentosa caused by mutation in ZNF513"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 58", "shortest_name_length": 4}
{"curie": "UMLS:C1335130", "names": ["Orbit Paraganglioma", "Orbital Paraganglioma", "Paraganglioma of Orbit", "Paraganglioma of the Orbit"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Orbit Paraganglioma", "shortest_name_length": 19}
{"curie": "UMLS:C3899267", "names": ["Encephalopathy of Prematurity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Encephalopathy of Prematurity", "shortest_name_length": 29}
{"curie": "MONDO:0000769", "names": ["chicken egg allergy", "Gallus gallus egg allergy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chicken egg allergy", "shortest_name_length": 19}
{"curie": "MONDO:0007646", "names": ["NMAN", "ARAN-NM", "ARCMT2-NM", "Gamstorp-Wohlfart syndrome", "GAMSTORP-WOHLFART SYNDROME", "myokymia, myotonia and muscle wasting", "Myokymia, myotonia and muscle wasting", "myokymia, myotonia, and muscle wasting", "MYOKYMIA, MYOTONIA, AND MUSCLE WASTING", "autosomal recessive neuromyotonia and axonal neuropathy", "NEUROMYOTONIA AND AXONAL NEUROPATHY, AUTOSOMAL RECESSIVE", "autosomal recessive axonal neuropathy with neuromyotonia", "Autosomal recessive neuromyotonia with axonal neuropathy", "neuromyotonia and axonal neuropathy, autosomal recessive", "Autosomal recessive axonal neuropathy with neuromyotonia", "Autosomal recessive axonal neuropathy with neuromyotonia (disorder)", "Autosomal recessive Charcot-Marie-Tooth disease type 2 with neuromyotonia", "autosomal recessive Charcot-Marie-Tooth disease type 2 with neuromyotonia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gamstorp-Wohlfart syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0009021", "names": ["TORIELLO-CAREY SYNDROME", "Toriello-Carey syndrome", "Toriello Carey syndrome", "Toriello-Carey Syndrome", "Toriello Carey syndrome (disorder)", "Toriello Carey syndrome (diagnosis)", "corpus callosum agenesis facial anomalies Robin sequence", "corpus callosum agenesis-facial anomalies-Robin sequence syndrome", "corpus callosum agenesis-blepharophimosis-Robin sequence syndrome", "Corpus callosum agenesis-blepharophimosis-Robin sequence syndrome", "agenesis of corpus callosum with facial anomalies and Robin sequence", "Corpus Callosum, Agenesis of, with Facial Anomalies and Robin Sequence", "corpus callosum, agenesis of, with facial anomalies and ROBIN sequence", "CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Toriello-Carey syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0015908", "names": ["CHROMOMYCOSIS", "Chromomycosis", "Chromomycoses", "chromomycosis", "mossy foot disease", "Mossy foot disease", "Chromoblastomycoses", "Chromoblastomycosis", "CHROMOBLASTOMYCOSIS", "chromoblastomycosis", "Dermatitis Verrucosa", "dermatitis Verrucosa", "Dermatitis verrucosa", "Chromomycosis, unspecified", "chromoblastomycosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromomycosis", "shortest_name_length": 13}
{"curie": "MONDO:0004174", "names": ["Endometrioid adenocarcinoma, secretory variant", "secretory uterine corpus endometrioid adenocarcinoma", "Secretory Uterine Corpus Endometrioid Adenocarcinoma", "endometrial endometrioid adenocarcinoma, secretory variant", "Endometrial Endometrioid Adenocarcinoma, Secretory Variant", "Endometrioid adenocarcinoma, secretory variant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secretory uterine corpus endometrioid adenocarcinoma", "shortest_name_length": 46}
{"curie": "MONDO:0017100", "names": ["neutropenia-monocytopenia-deafness syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neutropenia-monocytopenia-deafness syndrome", "shortest_name_length": 43}
{"curie": "UMLS:C4316897", "names": ["Atrophic Arthritis", "Atrophic arthritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atrophic arthritis", "shortest_name_length": 18}
{"curie": "MONDO:0016662", "names": ["Idiopathic relapsing pericarditis", "idiopathic relapsing pericarditis", "pericarditis idiopathic recurrent", "idiopathic recurrent pericarditis", "Idiopathic recurrent pericarditis", "Idiopathic recurrent pericarditis (disorder)", "Idiopathic recurrent pericarditis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic recurrent pericarditis", "shortest_name_length": 33}
{"curie": "MONDO:0018025", "names": ["Actinic reticuloid", "actinic reticuloid", "reticuloid; actinic", "Chronic Actinic Dermatitis", "chronic actinic dermatitis", "Chronic actinic dermatitis", "Dermatitis, Chronic Actinic", "Actinic Reticuloid Syndrome", "Actinic Dermatitis, Chronic", "Reticuloid Syndrome, Actinic", "Chronic Actinic Dermatitides", "Syndrome, Actinic Reticuloid", "Actinic Reticuloid Syndromes", "Actinic Dermatitides, Chronic", "Syndromes, Actinic Reticuloid", "Reticuloid Syndromes, Actinic", "Dermatitides, Chronic Actinic", "Actinic reticuloid (disorder)", "actinic reticuloid (diagnosis)", "CAD - Chronic actinic dermatitis", "chronic photosensitivity dermatitis", "Chronic photosensitivity dermatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic actinic dermatitis", "shortest_name_length": 18}
{"curie": "MONDO:0020558", "names": ["CMT2K", "Charcot-Marie-Tooth disease type 2K", "Charcot-Marie-Tooth Disease Type 2K", "autosomal dominant Charcot-Marie-Tooth disease type 2K", "Autosomal dominant Charcot-Marie-Tooth disease type 2K", "Charcot-Marie-Tooth Disease, Autosomal Dominant, Type 2k", "CHARCOT-MARIE-TOOTH DISEASE, AUTOSOMAL DOMINANT, TYPE 2K", "Autosomal dominant Charcot-Marie-Tooth disease type 2K (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant Charcot-Marie-Tooth disease type 2K", "shortest_name_length": 5}
{"curie": "MONDO:0011285", "names": ["ARMD1", "age related maculopathy 1", "MACULOPATHY, AGE-RELATED, 1", "Maculopathy, Age-Related, 1", "maculopathy, age-related, 1", "macular degeneration, age-related", "age related macular degeneration 1", "Macular Degeneration, Age-Related, 1", "macular degeneration, age-related, 1", "MACULAR DEGENERATION, AGE-RELATED, 1", "age related macular degeneration type 1", "macular Degeneration, age-related, type 1", "macular degeneration, age-related, reduced risk of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "age related macular degeneration 1", "shortest_name_length": 5}
{"curie": "UMLS:C4764254", "names": ["Platinum-Resistant Lung Small Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Platinum-Resistant Lung Small Cell Carcinoma", "shortest_name_length": 44}
{"curie": "UMLS:C0595876", "names": ["CALCIUM INTOXICATION", "Calcium intoxication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Calcium intoxication", "shortest_name_length": 20}
{"curie": "UMLS:C0333884", "names": ["Urothelial cell atypia", "Transitional Cell Atypia", "Transitional cell atypia", "Atypia, transitional cell", "Transitional cell atypia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transitional cell atypia", "shortest_name_length": 22}
{"curie": "MONDO:0040566", "names": ["disorder of glutathione metabolism", "inborn error of glutathione metabolism", "Inborn error of glutathione metabolism", "inherited glutathione metabolism disease", "glutathione metabolism disorder, inherited", "Inborn error of glutathione metabolism, NOS", "inborn error of glutathione metabolic process", "inborn glutathione metabolic process disorder", "Inborn error of glutathione metabolism (disorder)", "rare inborn error of glutathione metabolic process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited glutathione metabolism disease", "shortest_name_length": 34}
{"curie": "MONDO:0001220", "names": ["HYPOPARATHYROID", "hypoparathyroid", "Deficiency of PTH", "HYPOPARATHYROIDISM", "Hypoparathyroidism", "hypoparathyroidism", "deficiency; parathyroid", "parathyroid; deficiency", "Low parathyroid hormone", "Hypoparathyroidism, NOS", "Deficiency of parathyrin", "parathyroid; insufficiency", "insufficiency; parathyroid", "Hypoparathyroidism (disorder)", "parathyroid, underactivity of", "hypoparathyroidism (diagnosis)", "Hypoparathyroidism, unspecified", "Deficiency of parathyroid hormone", "Decreased parathyroid hormone secretion", "hypoparathyroidism, idiopathic (subtype)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypoparathyroidism", "shortest_name_length": 15}
{"curie": "UMLS:C0019287", "names": ["Epigastric Hernia", "hernia epigastric", "epigastric hernia", "Epigastric hernia", "epigastric hernias", "HERNIA, EPIGASTRIC", "Hernia, epigastric", "abdomen hernia epigastric", "Fatty hernia of linea alba", "Epigastric hernia (disorder)", "epigastric hernia (diagnosis)", "abdomen hernia epigastric (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epigastric hernia", "shortest_name_length": 17}
{"curie": "MONDO:0007272", "names": ["HCVAD", "Hereditary hypercarotenemia and vitamin A deficiency", "hereditary hypercarotenemia and vitamin A deficiency", "Hereditary hypercarotenaemia and vitamin A deficiency", "CAROTENOIDS, PLASMA LEVEL OF, QUANTITATIVE TRAIT LOCUS 1", "Carotenoids, plasma level of, quantitative trait locus 1", "hypercarotenemia and vitamin A deficiency, autosomal dominant", "HYPERCAROTENEMIA AND VITAMIN A DEFICIENCY, AUTOSOMAL DOMINANT", "Hypercarotenemia And Vitamin A Deficiency, Autosomal Dominant", "Hereditary hypercarotenemia and vitamin A deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary hypercarotenemia and vitamin A deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C1710418", "names": ["Thyroid Gland Teratoma", "Primary Thyroid Gland Teratoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Teratoma", "shortest_name_length": 22}
{"curie": "UMLS:C1332053", "names": ["AIDS-Related Oropharyngeal Candidiasis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Oropharyngeal Candidiasis", "shortest_name_length": 38}
{"curie": "UMLS:C5446482", "names": ["Unresectable Anal Canal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Anal Canal Squamous Cell Carcinoma", "shortest_name_length": 47}
{"curie": "MONDO:0008196", "names": ["Parastremmatic dwarfism", "PARASTREMMATIC DWARFISM", "parastremmatic dwarfism", "parastremmatic dysplasia", "Parastremmatic dysplasia", "Parastremmatic dwarfism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parastremmatic dwarfism", "shortest_name_length": 23}
{"curie": "MONDO:0008881", "names": ["Kyphomelic dysplasia", "KYPHOMELIC DYSPLASIA", "kyphomelic dysplasia", "Kyphomelic dysplasia (disorder)", "congenital bowing with short bones", "BOWING, CONGENITAL, WITH SHORT BONES", "Bowing, congenital, with short bones", "bowing, congenital, with short bones"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kyphomelic dysplasia", "shortest_name_length": 20}
{"curie": "MONDO:0001617", "names": ["transient global amnesia", "global transient amnesia", "Transient global amnesia", "Transient Global Amnesia", "Amnesia, Transient Global", "Global Amnesia, Transient", "transient global; amnesia", "amnesia; transient global", "TGA (Transient Global Amnesia)", "TGA - transient global amnesia", "TGA - Transient global amnesia", "TGAs (Transient Global Amnesia)", "transient global amnesia (disease)", "Transient global amnesia (finding)", "transient global amnesia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transient global amnesia", "shortest_name_length": 24}
{"curie": "MONDO:0043135", "names": ["microcephaly microphthalmos blindness", "Microcephaly microphthalmos blindness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly microphthalmos blindness", "shortest_name_length": 37}
{"curie": "MONDO:0019554", "names": ["idiopathic localized lipodystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic localized lipodystrophy", "shortest_name_length": 34}
{"curie": "MONDO:0007921", "names": ["Yns", "YNS", "yellow nail", "nail yellow", "yellow nails", "nail yellowing", "nails yellowing", "Yellow nail syndrome", "yellow nail syndrome", "YELLOW NAIL SYNDROME", "nail syndrome yellow", "Yellow Nail Syndrome", "syndrome; yellow nail", "Nail Syndrome, Yellow", "yellow nail; syndrome", "Yellow Nail Syndromes", "nails syndrome yellow", "Syndrome, Yellow Nail", "Nail Syndromes, Yellow", "Syndromes, Yellow Nail", "lymphedema and Yellow nails", "Lymphedema And Yellow Nails", "LYMPHEDEMA AND YELLOW NAILS", "Lymphedema with yellow nails", "lymphedema with yellow nails", "yellow nail syndrome (diagnosis)", "Hereditary lymphedema and yellow nails", "Hereditary lymphoedema and yellow nails", "Hereditary lymphedema and yellow nails (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "yellow nail syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0014140", "names": ["MDDGA14", "muscle-eye-brain-GMPPB related", "congenital muscular dystrophy-dystroglycanopathy A14", "Walker-Warburg syndrome or muscle-eye-brain disease GMPPB-related", "Walker-Warburg syndrome or muscle-eye-brain disease, GMPPB-related", "WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, GMPPB-RELATED", "congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A14", "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A14", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 14", "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A14", "shortest_name_length": 7}
{"curie": "MONDO:0007937", "names": ["HOMG2", "renal hypomagnesemia 2", "hypomagnesemia 2, renal", "Renal magnesium wasting", "Hypomagnesemia 2, renal", "HYPOMAGNESEMIA 2, RENAL", "Magnesium wasting, renal", "MAGNESIUM WASTING, RENAL", "magnesium wasting, renal", "Renal hypomagnesemia type 2", "renal hypomagnesemia type 2", "FXYD2 primary hypomagnesemia", "Magnesium loss, isolated renal", "MAGNESIUM LOSS, ISOLATED RENAL", "magnesium loss, isolated renal", "Isolated renal magnesium wasting", "isolated renal magnesium wasting", "HOMG2 - renal hypomagnesemia type 2", "HOMG2 - renal hypomagnesaemia type 2", "FXYD2 familial primary hypomagnesemia", "Isolated autosomal dominant hypomagnesemia", "isolated autosomal dominant hypomagnesemia", "Isolated autosomal dominant hypomagnesaemia", "primary hypomagnesemia caused by mutation in FXYD2", "familial primary hypomagnesemia caused by mutation in FXYD2", "Autosomal dominant primary hypomagnesemia with hypocalciuria", "autosomal dominant primary hypomagnesemia with hypocalciuria", "Autosomal dominant primary hypomagnesaemia with hypocalciuria", "Autosomal dominant primary hypomagnesemia with hypocalciuria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal hypomagnesemia 2", "shortest_name_length": 5}
{"curie": "UMLS:C3536718", "names": ["Growth Hormone Secretion Abnormality"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Growth Hormone Secretion Abnormality", "shortest_name_length": 36}
{"curie": "MONDO:0022869", "names": ["coronary arteries congenital malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coronary arteries congenital malformation", "shortest_name_length": 41}
{"curie": "MONDO:0000920", "names": ["Duodenal mass", "DUODENAL MASS", "duodenal mass", "tumor duodenal", "Duodenal tumor", "duodenum tumor", "duodenal tumor", "Duodenal Tumor", "Duodenal cancer", "duodenal cancer", "duodenum tumors", "duodenum cancer", "duodenum tumours", "Duodenal Neoplasm", "duodenal neoplasm", "Tumor of Duodenum", "Tumor of duodenum", "Duodenal neoplasm", "Duodenal Neoplasms", "duodenal neoplasms", "Tumour of duodenum", "Neoplasm, Duodenal", "cancer of duodenum", "Neoplasms, Duodenal", "neoplasm of duodenum", "Neoplasm of Duodenum", "Neoplasm of duodenum", "Tumor of the Duodenum", "Duodenal neoplasm NOS", "cancer of the duodenum", "Duodenal malignant tumor", "Malignant Duodenal Tumor", "Neoplasm of the Duodenum", "malignant duodenal tumor", "malignant duodenal neoplasm", "malignant duodenum neoplasm", "malignant tumor of duodenum", "Malignant Duodenal Neoplasm", "Malignant tumor of duodenum", "Malignant Tumor of Duodenum", "Malignant tumour of duodenum", "malignant neoplasm of duodenum", "Malignant neoplasm of duodenum", "Malignant Neoplasm of Duodenum", "Malignant Tumor of the Duodenum", "malignant tumor of the duodenum", "Neoplasm of duodenum (disorder)", "neoplasm of duodenum (diagnosis)", "malignant neoplasm of the duodenum", "Malignant neoplasm of duodenum NOS", "Malignant Neoplasm of the Duodenum", "Malignant tumor of duodenum (disorder)", "malignant neoplasm of duodenum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "duodenum cancer", "shortest_name_length": 13}
{"curie": "UMLS:C0520724", "names": ["retinal cyst", "cyst; retina", "retina; cyst", "Retinal cyst", "Cyst of retina", "Retinal cyst, NOS", "retinal cyst (diagnosis)", "Cyst of retina (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retinal cyst", "shortest_name_length": 12}
{"curie": "UMLS:C4331759", "names": ["WT1 Syndromes", "WT1 Gene Syndromes", "Wilms Tumor 1 Gene Syndromes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wilms Tumor 1 Gene Syndromes", "shortest_name_length": 13}
{"curie": "MONDO:0017531", "names": ["postaxial polydactyly type A, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postaxial polydactyly type A, unilateral", "shortest_name_length": 40}
{"curie": "MONDO:0042603", "names": ["Sanderson-Fraser syndrome", "Sanderson Fraser syndrome", "Proptosis, Robin association, clenched hands, and multiple abnormalities", "proptosis, Robin association, clenched hands, and multiple abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sanderson-Fraser syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0002641", "names": ["subclavian; aneurysm", "aneurysm; subclavian", "a.subclavia; aneurysm", "Subclavian artery aneurysm", "subclavian artery aneurysm", "aneurysm; subclavian artery", "Aneurysm of subclavian artery", "aneurysm of subclavian artery", "Aneurysm of subclavian artery (disorder)", "aneurysm of subclavian artery (diagnosis)", "aneurysm of subclavian artery (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subclavian artery aneurysm", "shortest_name_length": 20}
{"curie": "MONDO:0011425", "names": ["CMD1H", "dilated cardiomyopathy 1H", "cardiomyopathy, dilated, 1H", "Cardiomyopathy, Dilated, 1h", "CARDIOMYOPATHY, DILATED, 1H", "dilated cardiomyopathy type 1H", "Idiopathic dilation cardiomyopathy", "CARDIOMYOPATHY, DILATED, 1H (disorder)", "Dilated cardiomyopathy with conduction defect", "dilated cardiomyopathy with conduction defect", "cardiomyopathy, dilated, with conduction defect", "Cardiomyopathy, Dilated, With Conduction Defect", "CARDIOMYOPATHY, DILATED, WITH CONDUCTION DEFECT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1H", "shortest_name_length": 5}
{"curie": "UMLS:C0278835", "names": ["Prostate cancer stage II", "stage II prostate cancer", "prostate cancer, stage II", "Prostatic cancer stage II", "stage II cancer of the prostate", "cancer of the prostate, stage II", "stage II carcinoma of the prostate", "Carcinoma of the prostate stage II", "carcinoma of the prostate, stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carcinoma of the prostate stage II", "shortest_name_length": 24}
{"curie": "MONDO:0020789", "names": ["PTORCH1", "pseudo-TORCH syndrome", "pseudo-TORCH syndrome 1", "PSEUDO-TORCH SYNDROME 1", "pseudo-TORCH syndrome type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudo-TORCH syndrome 1", "shortest_name_length": 7}
{"curie": "UMLS:C5231079", "names": ["Syringocystadenocarcinoma Papilliferum", "Syringocystadenocarcinoma papilliferum", "Syringocystadenocarcinoma papilliferum (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Syringocystadenocarcinoma papilliferum", "shortest_name_length": 38}
{"curie": "UMLS:C1514688", "names": ["Radiation-Induced DNA Damage", "Radiation Induced DNA Damage", "DNA Damage, Radiation Induced", "Genotoxicity, Radiation Induced"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radiation Induced DNA Damage", "shortest_name_length": 28}
{"curie": "MONDO:0006945", "names": ["Renal artery stenosis", "stenosis renal artery", "Stenosis;artery;renal", "Renal Artery Stenosis", "RENAL ARTERY STENOSIS", "stenosis artery renal", "renal artery stenosis", "artery renal stenosis", "Renal Artery Stenoses", "Stenosis, Renal Artery", "Stenoses, Renal Artery", "stenosis; renal artery", "renal artery; stenosis", "a.renalis; obstruction", "arteries renal stenosis", "stenosis; artery, renal", "artery; stenosis, renal", "Renal Artery Obstruction", "Renal artery obstruction", "renal artery obstruction", "obstruction; renal artery", "Renal Artery Obstructions", "Obstruction, Renal Artery", "Renal artery stenosis NOS", "Obstructions, Renal Artery", "Renal artery stenosis, NOS", "Narrowing of kidney artery", "RAS - Renal artery stenosis", "Renal artery stenosis (disorder)", "renal artery stenosis (diagnosis)", "Renal artery stenosis of unknown cause", "Renal artery stenosis of unknown cause (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal artery obstruction", "shortest_name_length": 21}
{"curie": "MONDO:0010463", "names": ["X-linked dominant chondrodysplasia Chassaing Lacombe type", "X-linked dominant chondrodysplasia, Chassaing-Lacombe type", "X-linked dominant chondrodysplasia Chassaing Lacombe type (disorder)", "X-linked dominant chondrodysplasia-hydrocephaly-microphthalmia syndrome", "CHONDRODYSPLASIA WITH PLATYSPONDYLY, DISTINCTIVE BRACHYDACTYLY, HYDROCEPHALY, AND MICROPHTHALMIA", "chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia", "chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked dominant chondrodysplasia, Chassaing-Lacombe type", "shortest_name_length": 57}
{"curie": "UMLS:C4054381", "names": ["Nephrotic Syndrome - ITGB4 Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - ITGB4 Associated", "shortest_name_length": 37}
{"curie": "MONDO:0022545", "names": ["Barnicoat-Baraitser syndrome", "Barnicoat Baraitser syndrome", "polysyndactyly overgrowth syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Barnicoat Baraitser syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0017400", "names": ["MTCHRS", "Mitchell-Riley syndrome", "Mitchell-Riley Syndrome", "MITCHELL-RILEY SYNDROME", "hypoplastic pancreas-intestinal atresia-hypoplastic gallbalder syndrome", "hypoplastic pancreas-intestinal atresia-hypoplastic gallbladder syndrome", "DIABETES, NEONATAL, WITH PANCREATIC HYPOPLASIA, INTESTINAL ATRESIA, AND GALLBLADDER APLASIA OR HYPOPLASIA", "diabetes, neonatal, with pancreatic hypoplasia, intestinal atresia, and gallbladder aplasia or hypoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypoplastic pancreas-intestinal atresia-hypoplastic gallbalder syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0009683", "names": ["LGMD2H", "LGMDR8", "LGMD type 2H", "Sarcotubular myopathy", "sarcotubular myopathy", "SARCOTUBULAR MYOPATHY", "TRIM32-related LGMD R8", "LGMD due to TRIM32 deficiency", "Sarcotubular myopathy (disorder)", "Muscular dystrophy Hutterite type", "muscular dystrophy Hutterite type", "MUSCULAR DYSTROPHY, HUTTERITE TYPE", "Muscular Dystrophy, Hutterite Type", "muscular dystrophy, Hutterite type", "Hutterite type of muscular dystrophy", "muscular dystrophy limb-girdle type 2H", "Limb-girdle muscular dystrophy type 2H", "limb-girdle muscular dystrophy type 2H", "Muscular dystrophy, limb-girdle type 2H", "Muscular Dystrophy, Limb-Girdle, Type 2H", "muscular dystrophy, limb-girdle, type 2H", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2H", "Hutterite type of muscular dystrophy (disorder)", "TRIM32-related limb-girdle muscular dystrophy R8", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 8", "muscular dystrophy, limb-girdle, autosomal recessive 8", "Limb-girdle muscular dystrophy due to TRIM32 deficiency", "limb-girdle muscular dystrophy due to TRIM32 deficiency", "TRIM32 autosomal recessive limb-girdle muscular dystrophy", "Autosomal recessive limb-girdle muscular dystrophy type 2H", "autosomal recessive limb-girdle muscular dystrophy type 2H", "autosomal recessive limb-girdle muscular dystrophy caused by mutation in TRIM32"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive limb-girdle muscular dystrophy type 2H", "shortest_name_length": 6}
{"curie": "MONDO:0016190", "names": ["qualitative or quantitative defects of protein ZASP"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of protein ZASP", "shortest_name_length": 51}
{"curie": "UMLS:C5206744", "names": ["Severe Chronic Active EBV Infection", "Severe Chronic Active Epstein-Barr Virus Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Severe Chronic Active EBV Infection", "shortest_name_length": 35}
{"curie": "UMLS:C1512432", "names": ["High Grade Burkitt-Like Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Burkitt-Like Lymphoma", "shortest_name_length": 32}
{"curie": "UMLS:C0038538", "names": ["Subdural Effusion", "Subdural effusion", "effusion subdural", "subdural effusion", "Effusion, Subdural", "effusions subdural", "Subdural effusion (disorder)", "Subdural Cerebrospinal Fluid Leakage", "Cerebrospinal Fluid Leakage, Subdural", "Subdural Cerebrospinal Fluid Effusion", "Cerebrospinal Fluid Effusion, Subdural"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subdural Effusion", "shortest_name_length": 17}
{"curie": "UMLS:C2170313", "names": ["renal transplant failure", "Renal transplant failure", "renal transplant failure (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal transplant failure", "shortest_name_length": 24}
{"curie": "MONDO:0004285", "names": ["IPMN", "Pancreatic Intraductal Papillary-Colloid Carcinoma", "pancreatic intraductal papillary-colloid carcinoma", "intraductal papillary-colloid carcinoma of pancreas", "Pancreatic Intraductal Papillary-Mucinous Carcinoma", "pancreatic intraductal papillary-mucinous carcinoma", "pancreatic intraductal papillary mucinous carcinoma", "Pancreatic intraductal papillary mucinous carcinoma", "Intraductal Papillary-Colloid Carcinoma of Pancreas", "Intraductal papillary mucinous carcinoma of pancreas", "Intraductal Papillary-Mucinous Carcinoma of Pancreas", "intraductal papillary mucinous carcinoma of pancreas", "Pancreatic Intraductal Papillary-Colloidal Carcinoma", "Intraductal Papillary-mucinous carcinoma of pancreas", "intraductal papillary-mucinous carcinoma of pancreas", "pancreatic intraductal papillary-colloidal carcinoma", "Intraductal papillary-mucinous carcinoma of pancreas", "intraductal papillary-colloidal carcinoma of pancreas", "Intraductal Papillary-Colloidal Carcinoma of Pancreas", "Intraductal Papillary-Colloid Carcinoma of the Pancreas", "intraductal papillary-colloid carcinoma of the pancreas", "Intraductal Papillary-Mucinous Carcinoma of the Pancreas", "intraductal papillary-mucinous carcinoma of the pancreas", "intraductal papillary-colloidal carcinoma of the pancreas", "Intraductal Papillary-Colloidal Carcinoma of the Pancreas", "intraductal papillary-mucinous carcinoma of pancreas (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic intraductal papillary-mucinous carcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0012745", "names": ["CMD1Z", "dilated cardiomyopathy 1Z", "cardiomyopathy, dilated, 1Z", "Cardiomyopathy, Dilated, 1z", "CARDIOMYOPATHY, DILATED, 1Z", "dilated cardiomyopathy type 1Z", "cardiomyopathy, dilated, type 1Z", "TNNC1 familial isolated dilated cardiomyopathy", "familial isolated dilated cardiomyopathy caused by mutation in TNNC1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1Z", "shortest_name_length": 5}
{"curie": "MONDO:0056822", "names": ["Oppenheim", "Ziehen-Oppenheim", "OPPENHEIM DISEASE", "Oppenheim disease", "Oppenheim Disease", "Oppenheims Disease", "amyotonia congenita", "Amyotonia congenita", "oppenheim's disease", "Oppenheim's Disease", "Oppenheim's disease", "Amyotonia Congenita", "AMYOTONIA CONGENITA", "congenital; amyotonia", "amyotonia; congenital", "Oppenheim's amyotonia", "floppy amyotonic infant", "Amyotonia congenita (disorder)", "amyotonia congenita (diagnosis)", "congenital atonic pseudoparalysis", "Congenital atonic pseudoparalysis", "Oppenheim's disease (amyotonia congenita)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyotonia congenita", "shortest_name_length": 9}
{"curie": "MONDO:0008932", "names": ["PCD", "PREMATURE CENTROMERE DIVISION", "premature centromere division", "X-chromosome centromere peculiarity", "X-CHROMOSOME CENTROMERE PECULIARITY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "premature centromere division", "shortest_name_length": 3}
{"curie": "MONDO:0009018", "names": ["CCDF", "corneal dystrophy, central type", "CORNEAL DYSTROPHY, CENTRAL TYPE", "Corneal Dystrophy, Central Type", "Central Cloudy Dystrophy of Francois", "Central cloudy dystrophy of Francois", "Central cloudy dystrophy of François", "Francois' cloudy dystrophy of cornea", "central cloudy dystrophy of François", "central cloudy dystrophy of Francois", "CENTRAL CLOUDY DYSTROPHY OF FRANCOIS", "central cloudy corneal dystrophy of François", "Central cloudy corneal dystrophy of François", "Central cloudy dystrophy of Francois (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central cloudy dystrophy of François", "shortest_name_length": 4}
{"curie": "MONDO:0032872", "names": ["CILD42", "primary ciliary dyskinesia 42", "CILIARY DYSKINESIA, PRIMARY, 42", "ciliary dyskinesia, primary, 42", "primary ciliary dyskinesia 42 without situs inversus", "Ciliary Dyskinesia, Primary, 42, Without Situs Inversus", "CILIARY DYSKINESIA, PRIMARY, 42, WITHOUT SITUS INVERSUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ciliary dyskinesia, primary, 42", "shortest_name_length": 6}
{"curie": "UMLS:C4330970", "names": ["Stage II HPV-Mediated (p16-Positive) Oropharyngeal Throat Cancer", "Pathologic Stage II HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage II HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8", "shortest_name_length": 64}
{"curie": "MONDO:0008786", "names": ["B6-responsive sideroblastic anemia", "vitamin B6 responsive sideroblastic anemia", "Pyridoxine-responsive sideroblastic anemia", "pyridoxine-responsive sideroblastic anemia", "Pyridoxine responsive sideroblastic anemia", "Pyridoxine responsive sideroblastic anaemia", "Sideroblastic anemia, pyridoxine responsive", "Pyridoxine-responsive sideroblastic anaemia", "sideroblastic; anemia, pyridoxine-responsive", "anemia; sideroblastic, pyridoxine-responsive", "anemia congenital sideroblastic B6-responsive", "anemia, congenital sideroblastic, B6-responsive", "Anemia, Congenital Sideroblastic, B6-Responsive", "ANEMIA, CONGENITAL SIDEROBLASTIC, B6-RESPONSIVE", "Pyridoxine-responsive sideroblastic anemia (disorder)", "pyridoxine-responsive sideroblastic anemia (diagnosis)", "X chromosome-linked pyridoxine responsive sideroblastic anemia", "sideroblastic anemia pyridoxine-responsive autosomal recessive", "X chromosome-linked pyridoxine responsive sideroblastic anaemia", "anemia, sideroblastic, pyridoxine-responsive, autosomal recessive", "Anemia, Sideroblastic, Pyridoxine-Responsive, Autosomal Recessive", "ANEMIA, SIDEROBLASTIC, PYRIDOXINE-RESPONSIVE, AUTOSOMAL RECESSIVE", "X chromosome-linked pyridoxine responsive sideroblastic anemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyridoxine-responsive sideroblastic anemia", "shortest_name_length": 34}
{"curie": "MONDO:0006254", "names": ["Intestinal Type Carcinoma", "intestinal type carcinoma", "Carcinoma, intestinal type", "Carcinoma - intestinal type", "intestinal-type adenocarcinoma", "Intestinal-type adenocarcinoma", "Intestinal Type Adenocarcinoma", "Intestinal-Type Adenocarcinoma", "intestinal type adenocarcinoma", "Adenocarcinoma, intestinal type", "Adenocarcinoma - intestinal type", "Adenocarcinoma, intestinal type (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intestinal type adenocarcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0007070", "names": ["Dercum", "Adiposalgia", "Adiposalgias", "Morbus Dercum", "Ander Syndrome", "Dercum disease", "Dercum Disease", "dercum disease", "Dercum, Morbus", "DERCUM DISEASE", "Morbus Dercums", "Disease, Dercum", "Anders Syndrome", "Dercums, Morbus", "dercums disease", "Dercums Disease", "DERCUM'S DISEASE", "Dercum's disease", "dercum's disease", "Dercum's Disease", "Anders Syndromes", "Syndrome, Anders", "dercum s disease", "Neurolipomatosis", "Ander's Syndrome", "adiposis dolorosa", "Disease, Dercum's", "Syndromes, Anders", "Adiposis Dolorosa", "ADIPOSIS DOLOROSA", "Adiposis dolorosa", "Syndrome, Ander's", "dolorosa; adiposis", "adiposis; dolorosa", "lipomatosis dolorosa", "Lipomatosis dolorosa", "Lipomatosis Dolorosa", "Decum Vitaut Syndrome", "Decum-Vitaut Syndrome", "dolorosa; lipomatosis", "lipomatosis; dolorosa", "Dolorosa, Lipomatosis", "Lipomatosis Dolorosas", "Syndrome, Decum-Vitaut", "Dolorosas, Lipomatosis", "Adipose Tissue Rheumatism", "adipose tissue rheumatism", "Adipose tissue rheumatism", "Tissue Rheumatism, Adipose", "Rheumatism, Adipose Tissue", "Adipose Tissue Rheumatisms", "Tissue Rheumatisms, Adipose", "Rheumatisms, Adipose Tissue", "adiposis dolorosa (diagnosis)", "Lipomatosis dolorosa (disorder)", "adiposis dolorosa (Dercum's disease)", "Lipomatosis (Check) dolorosa [Dercum]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adiposis dolorosa", "shortest_name_length": 6}
{"curie": "MONDO:0021070", "names": ["sublingual gland cancer", "Sublingual Gland Cancer", "Sublingual Gland Carcinoma", "sublingual gland carcinoma", "Carcinoma of sublingual gland", "carcinoma of sublingual gland", "Carcinoma of Sublingual Gland", "Carcinoma of the Sublingual Gland", "carcinoma of the sublingual gland", "Carcinoma of sublingual gland (disorder)", "Carcinoma of sublingual gland (diagnosis)", "malignant salivary gland neoplasm sublingual carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sublingual gland carcinoma", "shortest_name_length": 23}
{"curie": "UMLS:C0854954", "names": ["Ovarian germ cell teratoma benign"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian germ cell teratoma benign", "shortest_name_length": 33}
{"curie": "MONDO:0014547", "names": ["COXPD24", "combined oxidative phosphorylation deficiency 24", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 24", "Combined oxidative phosphorylation defect type 24", "combined oxidative phosphorylation defect type 24", "NARS2 combined oxidative phosphorylation deficiency", "combined oxidative phosphorylation deficiency type 24", "COXPD24 - combined oxidative phosphorylation defect type 24", "Combined oxidative phosphorylation defect type 24 (disorder)", "combined oxidative phosphorylation deficiency caused by mutation in NARS2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation defect type 24", "shortest_name_length": 7}
{"curie": "UMLS:C0349218", "names": ["Recurrent depressive disorder", "Recurrent depressive disorder, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent depressive disorder", "shortest_name_length": 29}
{"curie": "MONDO:0043424", "names": ["gi infection", "GI infection", "GI infections", "gi infections", "gastrointestinal infection", "infection gastrointestinal", "Digestive System Infection", "GASTROINTESTINAL INFECTION", "Gastrointestinal infection", "Gastrointestinal Infection", "digestive system infection", "gastrointestinal infections", "Gastrointestinal infections", "infection; gastrointestinal", "gastrointestinal; infection", "Infection of digestive system", "Gastrointestinal infection NOS", "Gastrointestinal tract infections", "gastrointestinal system infection", "Gastrointestinal System Infection", "Recurrent infection of the GI tract", "Infection of gastrointestinal tract", "infection of gastrointestinal tract", "digestive system infectious disorder", "Infectious disease of digestive tract", "Recurrent gastrointestinal infections", "Gastrointestinal infections, recurrent", "gastrointestinal infections (diagnosis)", "Infection of digestive system (disorder)", "Gastrointestinal tract infections, recurrent", "Infection of gastrointestinal tract (disorder)", "Infectious disease of digestive tract (disorder)", "Recurrent infection of the gastrointestinal tract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "digestive system infectious disorder", "shortest_name_length": 12}
{"curie": "MONDO:0001965", "names": ["Sclerokeratitis", "sclerokeratitis", "Keratitis sclerosing", "Sclerosing keratitis", "sclerosing keratitis", "keratitis; sclerosing", "sclerosing; keratitis", "Sclerokeratitis (disorder)", "sclerokeratitis (diagnosis)", "Sclerosing keratitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sclerosing keratitis", "shortest_name_length": 15}
{"curie": "MONDO:0008538", "names": ["GCA", "gca", "horton disease", "Horton Disease", "HORTON DISEASE", "Horton disease", "Hortons Disease", "Horton's Disease", "Horton's disease", "Horton’s disease", "horton's disease", "CRANIAL ARTERITIS", "cranial arteritis", "Cranial arteritis", "arteritis cranial", "Cranial Arteritis", "Horton’s syndrome", "Temporal Arteritis", "ARTERITIS TEMPORAL", "Horton's arteritis", "temporal arteritis", "ARTERITIS, CRANIAL", "arteritis temporal", "Arteritis, Cranial", "TEMPORAL ARTERITIS", "Temporal arteritis", "horton's arteritis", "Arteritis;temporal", "arteritis cranialis", "arteritis; temporal", "Cranial Arteritides", "ARTERITIS, TEMPORAL", "Arteritis, Temporal", "temporal; arteritis", "Giant cell arteritis", "Temporal Arteritides", "Giant Cell Arteritis", "Arteritides, Cranial", "giant cell arteritis", "GIANT CELL ARTERITIS", "arteritis cell giant", "arteritis temporalis", "ARTERITIS, GIANT CELL", "giant cell; arteritis", "ARTERITIS OF THE AGED", "arteritis; giant cell", "Arteritis, Giant Cell", "Arteritides, Temporal", "polymyalgia rheumatica", "Giant Cell Arteritides", "POLYMYALGIA RHEUMATICA", "TA - Temporal arteritis", "Arteritides, Giant Cell", "GCA - Giant cell arteritis", "Temporal arteritis syndrome", "Horton's temporal arteritis", "Horton Giant Cell Arteritis", "temporal artery inflammation", "Giant Cell Arteritis, Horton", "Arteritis, Giant Cell, Horton", "Temporal giant cell arteritis", "Giant cell arteritis syndrome", "Horton's giant cell arteritis", "Horton's Giant Cell Arteritis", "Temporal arteritis (disorder)", "cranial arteritis (diagnosis)", "temporal arteritis (diagnosis)", "Arteritis, Giant Cell, Horton's", "inflammation of temporal artery", "giant cell arteritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "temporal arteritis", "shortest_name_length": 3}
{"curie": "UMLS:C2752056", "names": ["Nasopharyngeal Hairy Polyp", "Nasopharyngeal hairy polyp", "Nasopharyngeal Dermoid Polyp", "Nasopharyngeal Teratoid Polyp"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasopharyngeal hairy polyp", "shortest_name_length": 26}
{"curie": "MONDO:0001978", "names": ["Ureter cancer local", "Ureteric cancer local", "Ureter cancer regional", "Ureteric cancer regional", "regional ureteric cancer", "regional ureter carcinoma", "Regional Ureter Carcinoma", "regional Ureteric carcinoma", "Regional Ureteric Carcinoma", "regional ureteric carcinoma", "Local Malignant Ureter Tumor", "Local Malignant Ureteral Tumor", "Regional Malignant Ureter Tumor", "Local Malignant Ureter Neoplasm", "Regional Malignant Ureteral Tumor", "regional malignant ureteral tumor", "Local Malignant Ureteral Neoplasm", "Malignant neoplasm of ureter local", "Regional Malignant Ureter Neoplasm", "Regional Malignant Ureteral Neoplasm", "Malignant neoplasm of ureter regional"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "regional ureteric cancer", "shortest_name_length": 19}
{"curie": "MONDO:0001271", "names": ["Lens Subluxation", "lens subluxation", "Lens subluxation", "lens; subluxation", "Lens Subluxations", "subluxation; lens", "Subluxation, Lens", "Subluxations, Lens", "subluxation of lens", "Subluxation of lens", "lenticular subluxation", "Partially dislocated lens", "lens subluxation (disease)", "Partial dislocation of lens", "Subluxation of lens (disorder)", "subluxation of lens (diagnosis)", "lenticular subluxation (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lens subluxation", "shortest_name_length": 16}
{"curie": "UMLS:C0010828", "names": ["cytopenia", "CYTOPENIA", "Cytopenia", "cytopenias", "Cytopenias", "Cytopenia, NOS", "Cytopenia (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cytopenia", "shortest_name_length": 9}
{"curie": "MONDO:0017014", "names": ["chILD", "chILD syndrome", "ILD specific to childhood", "childhood interstitial lung disease", "pediatric interstitial lung disease", "Interstitial lung disease of childhood", "interstitial lung disease of childhood", "Interstitial lung diseases of childhood", "interstitial lung disease specific to childhood", "Interstitial lung disease of childhood (disorder)", "interstitial lung disease of childhood (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "interstitial lung disease specific to childhood", "shortest_name_length": 5}
{"curie": "UMLS:C0348993", "names": ["Penicillosis", "penicillosis", "Talaromycosis", "Penicilliosis", "talaromycosis", "Talaromyces infection", "Penicillium infection", "Penicillium; infection", "infection; Penicillium", "Talaromyces infections", "Penicillosis (disorder)", "Talaromycosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "talaromycosis", "shortest_name_length": 12}
{"curie": "UMLS:C1336385", "names": ["Stage IVB Mouth Verrucous Carcinoma", "Stage IVB Oral Cavity Verrucous Cancer", "Stage IVB Verrucous Carcinoma of Mouth", "Stage IVB Oral Cavity Verrucous Carcinoma", "Stage IVB Verrucous Carcinoma of the Mouth", "Stage IVB Verrucous Carcinoma of Oral Cavity", "stage IVB verrucous carcinoma of the oral cavity", "Stage IVB Verrucous Carcinoma of the Oral Cavity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Oral Cavity Verrucous Carcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C5418597", "names": ["Advanced Thyroid Gland Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Thyroid Gland Carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0003930", "names": ["Stage 0 Bladder Urothelial Cancer", "stage 0 bladder urothelial cancer", "stage 0 bladder urothelial carcinoma", "Stage 0 Bladder Urothelial Carcinoma", "Non-Invasive Bladder Urothelial Carcinoma", "non-invasive bladder urothelial carcinoma", "Bladder transitional cell carcinoma stage 0", "stage 0 bladder urothelial carcinoma aJCC v6", "Stage 0 Bladder Urothelial Carcinoma AJCC v7", "stage 0 bladder urothelial carcinoma aJCC v7", "Stage 0 Transitional Cell Carcinoma of Bladder", "stage 0 transitional cell carcinoma of bladder", "Stage 0 Transitional Cell Carcinoma of the Bladder", "stage 0 transitional cell carcinoma of the bladder", "Stage 0 Urinary Bladder Transitional Cell Carcinoma", "stage 0 urinary bladder transitional cell carcinoma", "stage 0 bladder urothelial carcinoma aJCC v6 and v7", "Stage 0 Bladder Urothelial Carcinoma AJCC v6 and v7", "Stage 0 Transitional Cell Carcinoma of Urinary Bladder", "stage 0 transitional cell carcinoma of urinary bladder", "stage 0 transitional cell carcinoma of the urinary bladder", "Stage 0 Transitional Cell Carcinoma of the Urinary Bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-invasive bladder urothelial carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0012277", "names": ["MFM4", "zaspopathy", "MFM, Zasp-related", "myofibrillar myopathy 4", "MYOPATHY, MYOFIBRILLAR, 4", "myopathy, myofibrillar, 4", "myofibrillar myopathy type 4", "myopathy, myofibrillar, type 4", "ZASP-related myofibrillar myopathy", "ZASP related myofibrillar myopathy", "Myopathy, Myofibrillar, Zasp-Related", "LDB3 myofibrillar myopathy (disease)", "Late-onset distal myopathy Markesbery Griggs type", "late-onset distal myopathy, Markesbery-Griggs type", "Late-onset distal myopathy, Markesbery-Griggs type", "myofibrillar myopathy (disease) caused by mutation in LDB3", "Late-onset distal myopathy Markesbery Griggs type (disorder)", "ZASP (Z-band alternatively spliced PDZ motif protein) related myofibrillar myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myofibrillar myopathy 4", "shortest_name_length": 4}
{"curie": "UMLS:C2981416", "names": ["Stage II Small Intestinal Gastrointestinal Stromal Tumor", "Stage II Small Intestinal Gastrointestinal Stromal Tumor (GIST)", "Stage II Small Intestinal Gastrointestinal Stromal Tumor AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Small Intestinal Gastrointestinal Stromal Tumor", "shortest_name_length": 56}
{"curie": "MONDO:0024883", "names": ["Metastatic", "Tumor embolus", "Tumor embolism", "Tumor Embolism", "Tumour embolus", "Tumor Embolisms", "Embolism, Tumor", "Tumour embolism", "metastatic tumor", "Embolisms, Tumor", "Metastatic Tumor", "Tumor, secondary", "Tumor, metastatic", "metastatic cancer", "Tumour, secondary", "Metastatic cancer", "METASTATIC DISEASE", "Metastatic disease", "cancer, metastatic", "metastatic disease", "Tumour, metastatic", "metastatic neoplasm", "Metastatic neoplasm", "Metastatic Neoplasm", "Neoplasm, secondary", "Neoplasm, metastatic", "neoplasm; metastatic", "Metastatic cancer NOS", "Metastatic disease NOS", "Tumor embolus (disorder)", "Metastatic Malignant Neoplasm", "metastasis from malignant neoplasm", "Neoplasm, metastatic (morphologic abnormality)", "metastasis from malignant neoplasm (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metastatic neoplasm", "shortest_name_length": 10}
{"curie": "UMLS:C4086611", "names": ["Mucolipidosis Type IIIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mucolipidosis Type IIIA", "shortest_name_length": 23}
{"curie": "UMLS:C0342387", "names": ["LH deficiency", "Lutropin Deficiency", "Luteinizing Hormone Deficiency", "Luteinising hormone deficiency", "Luteinizing hormone deficiency", "Luteinizing hormone (LH) deficiency", "LH - luteinizing hormone deficiency", "LH - luteinising hormone deficiency", "Luteinizing hormone deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "LH - luteinizing hormone deficiency", "shortest_name_length": 13}
{"curie": "MONDO:0003963", "names": ["diffuse infiltra. lymph. sydrome", "Diffuse infiltra. lymph. syndrome", "diffuse infiltra. lymph. syndrome", "diffuse infiltrative lymphocytosis syndrome", "Diffuse Infiltrative Lymphocytosis Syndrome", "Diffuse infiltrative lymphocytosis syndrome", "DILS - diffuse infiltrative lymphocytosis syndrome", "Diffuse infiltrative lymphocytosis syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diffuse infiltrative lymphocytosis syndrome", "shortest_name_length": 32}
{"curie": "MONDO:0001827", "names": ["piedra; alba", "tinea blanca", "Tinea blanca", "alba; piedra", "White piedra", "White Piedra", "white piedra", "Piedra, White", "blanca; tinea", "tinea; blanca", "White Piedras", "Piedras, White", "White piedra (disorder)", "white piedra (diagnosis)", "Piedra due to Trichosporon", "Piedra due to Trichosporon cutaneum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "white piedra", "shortest_name_length": 12}
{"curie": "UMLS:C5238243", "names": ["Unresectable Bladder Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Bladder Carcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0017875", "names": ["Black typhus", "Bolivian fever", "fever; Machupo", "Machupo; fever", "Machupo hemorrhagic fever", "hemorrhagic fever; Machupo", "Machupo haemorrhagic fever", "Bolivian Hemorrhagic Fever", "Bolivian hemorrhagic fever", "Machupo; hemorrhagic fever", "Hemorrhagic Fever, Bolivian", "Bolivian hemorrhagic; fever", "hemorrhagic fever; Bolivian", "fever; Bolivian hemorrhagic", "Bolivian; hemorrhagic fever", "Hemorrhagic fever, Bolivian", "Fever, Bolivian Hemorrhagic", "Bolivian haemorrhagic fever", "BHF - Bolivian hemorrhagic fever", "Hemorrhagic fever, Machupo virus", "virus; Machupo, hemorrhagic fever", "BHF - Bolivian haemorrhagic fever", "Bolivian hemorrhagic fever (disorder)", "Bolivian hemorrhagic fever (diagnosis)", "Hemorrhagic fever due to Machupo virus", "Haemorrhagic fever due to Machupo virus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bolivian hemorrhagic fever", "shortest_name_length": 12}
{"curie": "MONDO:0022461", "names": ["anophthalmia cleft palate micrognathia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anophthalmia cleft palate micrognathia", "shortest_name_length": 38}
{"curie": "MONDO:0011761", "names": ["DFNA21", "autosomal dominant deafness 21", "Deafness, Autosomal Dominant 21", "DEAFNESS, AUTOSOMAL DOMINANT 21", "deafness, autosomal dominant 21", "DEAFNESS, AUTOSOMAL DOMINANT 21 (disorder)", "autosomal dominant nonsyndromic deafness 21", "autosomal dominant nonsyndromic hearing loss 21", "autosomal dominant nonsyndromic deafness type 21"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 21", "shortest_name_length": 6}
{"curie": "MONDO:0005369", "names": ["NET G1", "Carcinoid", "CARCINOID", "carcinoid", "Carcinoids", "carcinoids", "CARCINOID TUMOR", "Carcinoid tumor", "carcinoid tumor", "Carcinoid Tumor", "Carcinoid tumors", "Tumor, Carcinoid", "carcinoid tumour", "Carcinoid tumour", "Carcinoid Tumors", "carcinoid tumors", "carcinoid tumours", "Carcinoid tumours", "Tumors, Carcinoid", "[M]Carcinoid tumors", "Carcinoid tumor NOS", "[M]Carcinoid tumours", "Carcinoid tumour NOS", "neuroendocrine tumor G1", "carcinoid tumor (disease)", "Carcinoid tumor (disorder)", "neuroendocrine neoplasm G1", "carcinoid tumor (diagnosis)", "Carcinoid tumor - morphology", "Carcinoid tumour - morphology", "neuroendocrine tumor carcinoid", "Enterochromaffin cell carcinoid", "Carcinoid tumor - morphology (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoid tumor", "shortest_name_length": 6}
{"curie": "UMLS:C1335493", "names": ["Primary T-Cell Breast Lymphoma", "Primary T-Cell Lymphoma of Breast", "Breast T-Cell Non-Hodgkin Lymphoma", "Breast T-Cell Non-Hodgkin's Lymphoma", "Primary T-Cell Lymphoma of the Breast", "T-Cell Non-Hodgkin's Lymphoma of the Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast T-Cell Non-Hodgkin Lymphoma", "shortest_name_length": 30}
{"curie": "UMLS:C4521829", "names": ["IV", "Stage IV Distal Bile Duct Cancer AJCC v8", "Stage IV Distal Bile Duct Carcinoma AJCC v8", "Stage IV Extrahepatic (Distal) Bile Duct Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Distal Bile Duct Cancer AJCC v8", "shortest_name_length": 2}
{"curie": "UMLS:C0276623", "names": ["Chronic viral hepatitis", "Chronic Viral Hepatitis", "chronic viral hepatitis", "hepatitis chronic viral", "hepatitis; virus, chronic", "Chronic viral hepatitis (disorder)", "chronic viral hepatitis (diagnosis)", "Chronic viral hepatitis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic viral hepatitis", "shortest_name_length": 23}
{"curie": "UMLS:C5555509", "names": ["Recurrent Pseudomyxoma Peritonei"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Pseudomyxoma Peritonei", "shortest_name_length": 32}
{"curie": "UMLS:C1334713", "names": ["Metastatic Bone Ewing Sarcoma", "Metastatic Bone Ewing's Sarcoma", "Metastatic Osseous Ewing's Sarcoma", "Metastatic Ewing's Sarcoma of Bone", "Metastatic Skeletal Ewing's Sarcoma", "Metastatic Ewing's Sarcoma of the Bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Bone Ewing Sarcoma", "shortest_name_length": 29}
{"curie": "MONDO:0013341", "names": ["CD320 methylmalonic acidemia", "Methylmalonic acidemia TCb1R type", "methylmalonic acidemia, TCbIR type", "Methylmalonic acidaemia TCb1R type", "methylmalonic acidemia, TCb1R type", "Methylmalonic acidemia, TCb1R type", "METHYLMALONIC ACIDEMIA, TCblR TYPE", "Methylmalonic acidemia, TCbIR type", "Methylmalonic Acidemia, TcblR Type", "methylmalonic acidemia, Tcblr type", "methylmalonic acidemia, TCblR type", "methylmalonic acidemia caused by mutation in CD320", "methylmalonic acidemia due to transcobalamin receptor defect", "Methylmalonic Aciduria due to Transcobalamin Receptor Defect", "methylmalonic aciduria due to transcobalamin receptor defect", "Methylmalonic aciduria due to transcobalamin receptor defect", "Methylmalonic aciduria due to transcobalamin receptor defect (disorder)", "METHYLMALONIC ACIDURIA, TRANSIENT, DUE TO TRANSCOBALAMIN RECEPTOR DEFECT", "methylmalonic aciduria, transient, due to transcobalamin receptor defect", "Methylmalonic Aciduria, Transient, due to Transcobalamin Receptor Defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "methylmalonic acidemia due to transcobalamin receptor defect", "shortest_name_length": 28}
{"curie": "UMLS:C3241936", "names": ["noncardiac pulmonary edema", "Noncardiogenic Pulmonary Edema", "Non-cardiogenic pulmonary edema", "Non-Cardiogenic Pulmonary Edema", "non-cardiogenic pulmonary edema", "Non-cardiogenic pulmonary oedema", "noncardiac pulmonary edema (diagnosis)", "Non-cardiogenic pulmonary edema (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-cardiogenic pulmonary edema", "shortest_name_length": 26}
{"curie": "MONDO:0001319", "names": ["Wall, Lateral", "Lateral wall of bladder", "Lateral Wall of bladder", "Lateral Wall of Bladder", "Lateral Wall of the Bladder", "bladder lateral wall cancer", "malignant tumor of lateral wall of bladder", "Malignant neoplasm of lateral wall of bladder", "malignant neoplasm of lateral wall of bladder", "Malignant neoplasm of lateral wall of urinary bladder", "malignant neoplasm of lateral wall of urinary bladder", "malignant neoplasm of lateral wall of bladder (diagnosis)", "Malignant neoplasm of lateral wall of urinary bladder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder lateral wall cancer", "shortest_name_length": 13}
{"curie": "UMLS:C0406047", "names": ["Local infection skin/subcut tissue NOS", "local infections skin and subcutaneous tissue", "Local Infection of Skin and Subcutaneous Tissue", "local infections of skin and subcutaneous tissue", "Unspecified local infection of skin and subcutaneous tissue", "Local infection of skin and subcutaneous tissue, unspecified", "local infections of skin and subcutaneous tissue (diagnosis)", "Local infection of the skin and subcutaneous tissue, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Local infection skin/subcut tissue NOS", "shortest_name_length": 38}
{"curie": "UMLS:C0338757", "names": ["continuous cannabis dependence", "Cannabis dependence, continuous", "Cannabis dependence, continuous use", "Cannabis Dependence, Continuous Use", "continuous cannabis dependence (diagnosis)", "Cannabis dependence, continuous (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cannabis dependence, continuous", "shortest_name_length": 30}
{"curie": "UMLS:C1516058", "names": ["Astler-Coller A Rectal Carcinoma", "Astler-Coller A Carcinoma of Rectum", "Astler-Coller A Carcinoma of the Rectum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Astler-Coller A Rectal Carcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C1518733", "names": ["Ovarian Sex Cord-Stromal Tumor Associated with Peutz-Jeghers Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Sex Cord-Stromal Tumor Associated with Peutz-Jeghers Syndrome", "shortest_name_length": 69}
{"curie": "UMLS:C0279986", "names": ["Leiomyosarcoma", "childhood leiomyosarcoma", "Childhood Leiomyosarcoma", "Pediatric Leiomyosarcoma", "pediatric leiomyosarcoma", "leiomyosarcoma, pediatric", "leiomyosarcoma, childhood", "sarcoma, leiomyo-, pediatric", "sarcoma, leiomyo-, childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Leiomyosarcoma", "shortest_name_length": 14}
{"curie": "MONDO:0011561", "names": ["AD6", "Alzheimer Disease 6", "Alzheimer disease 6", "ALZHEIMER DISEASE 6", "Alzheimer's disease 6", "Alzheimer disease type 6", "Alzheimer's disease type 6", "Alzheimer disease 6, late-onset", "Alzheimer disease 6, late onset", "Alzheimer Disease 6, Late-Onset", "ALZHEIMER DISEASE 6, LATE-ONSET", "plasma Beta-amyloid-42 level quantitative trait locus", "PLASMA BETA-AMYLOID-42 LEVEL QUANTITATIVE TRAIT LOCUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alzheimer disease 6", "shortest_name_length": 3}
{"curie": "MONDO:0017667", "names": ["isolated diffuse PPK", "isolated diffuse keratosis palmoplantaris", "isolated diffuse palmoplantar keratoderma", "isolated diffuse palmoplantar hyperkeratosis", "nonsyndromic diffuse palmoplantar keratoderma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated diffuse palmoplantar keratoderma", "shortest_name_length": 20}
{"curie": "MONDO:0003592", "names": ["Gastric Liposarcoma", "gastric liposarcoma", "stomach liposarcoma", "Stomach Liposarcoma", "liposarcoma of stomach", "Liposarcoma of Stomach", "liposarcoma of the stomach", "Liposarcoma of the stomach", "Liposarcoma of the Stomach", "liposarcoma of stomach (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric liposarcoma", "shortest_name_length": 19}
{"curie": "MONDO:0012272", "names": ["Mental retardation, keratoconus, febrile seizures, and sinoatrial block", "MENTAL RETARDATION, KERATOCONUS, FEBRILE SEIZURES, AND SINOATRIAL BLOCK", "mental retardation, keratoconus, febrile seizures, and sinoatrial block", "intellectual disability, keratoconus, febrile seizures, and sinoatrial block"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, keratoconus, febrile seizures, and sinoatrial block", "shortest_name_length": 71}
{"curie": "MONDO:0022871", "names": ["corpus callosum agenesis of blepharophimosis robin type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corpus callosum agenesis of blepharophimosis robin type", "shortest_name_length": 55}
{"curie": "UMLS:C4330472", "names": ["Accelerated Starvation", "Idiopathic Ketotic Hypoglycemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Idiopathic Ketotic Hypoglycemia", "shortest_name_length": 22}
{"curie": "MONDO:0006774", "names": ["habitual aborter", "Habitual aborter", "habitual abortion", "abortion habitual", "Habitual abortion", "Habitual Abortion", "Recurrent aborter", "Abortion;habitual", "ABORTION HABITUAL", "abortion recurrent", "Abortion, habitual", "recurrent abortion", "Recurrent abortion", "habitual; abortion", "Recurrent Abortion", "Habitual Abortions", "Abortion, Habitual", "habitual abortions", "abortion; habitual", "Abortion, Recurrent", "Recurrent Abortions", "recurrent abortions", "Recurrent miscarriage", "recurrent miscarriage", "Recurrent Miscarriage", "miscarriage recurrent", "Recurrent Miscarriages", "Miscarriage, Recurrent", "recurrent miscarriages", "chronic spontaneous abortion", "habitual spontaneous abortion", "Recurrent Early Pregnancy Loss", "abortion; habitual or recurrent", "habitual or recurrent; abortion", "Recurrent miscarriage (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "habitual spontaneous abortion", "shortest_name_length": 16}
{"curie": "MONDO:0024521", "names": ["AAA1", "abdominal aortic aneurysm", "aneurysm, abdominal aortic", "aortic aneurysm, familial abdominal 1", "Aortic Aneurysm, Familial Abdominal 1", "AORTIC ANEURYSM, FAMILIAL ABDOMINAL 1", "AORTIC ANEURYSM, FAMILIAL ABDOMINAL, 1", "aortic aneurysm, familial abdominal, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic aneurysm, familial abdominal, 1", "shortest_name_length": 4}
{"curie": "UMLS:C0686055", "names": ["ESOPHAGEAL METASTASIS", "Esophageal Metastasis", "Metastases to esophagus", "Metastases to Esophagus", "Metastasis to Esophagus", "Metastases to oesophagus", "Metastases to the Esophagus", "Metastasis to the Esophagus", "Metastatic Tumor to the Esophagus", "Metastatic Neoplasm to the Esophagus", "esophageal malignant neoplasm secondary", "Secondary malignant neoplasm of esophagus", "Secondary malignant neoplasm of oesophagus", "Metastatic malignant neoplasm to esophagus", "Metastatic malignant neoplasm of esophagus", "Metastatic malignant neoplasm of oesophagus", "Metastatic malignant neoplasm to oesophagus", "Metastatic Malignant Neoplasm in the Esophagus", "Secondary malignant neoplasm of esophagus, NOS", "Metastatic Malignant Neoplasm to the Esophagus", "Metastatic malignant neoplasm to esophagus, NOS", "Secondary malignant neoplasm of oesophagus, NOS", "Metastatic malignant neoplasm to oesophagus, NOS", "Secondary malignant neoplasm of esophagus (diagnosis)", "Metastatic malignant neoplasm to esophagus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to esophagus", "shortest_name_length": 21}
{"curie": "UMLS:C3266958", "names": ["Pre-engraftment immune reaction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pre-engraftment immune reaction", "shortest_name_length": 31}
{"curie": "MONDO:0005851", "names": ["Fisher Syndrome", "Fisher syndrome", "fisher syndrome", "Syndrome, Fisher", "syndrome, Fisher", "Fisher's syndrome", "fisher miller syndrome", "Miller-Fisher Syndrome", "Miller-Fisher syndrome", "cranial variant of GBS", "Miller Fisher syndrome", "miller-fisher syndrome", "Miller Fisher Syndrome", "syndrome miller fisher", "miller fisher syndrome", "Cranial variant of GBS", "syndrome, Miller Fisher", "Syndrome, Miller Fisher", "syndrome, Miller-Fisher", "Syndrome, Miller-Fisher", "Fisher's syndrome (disorder)", "Miller-Fisher syndrome (diagnosis)", "Cranial variant of Guillain-Barré syndrome", "cranial variant of Guillain-Barré syndrome", "cranial variant of Guillain-Barre syndrome", "Ophthalmoplegia, ataxia, areflexia syndrome", "ophthalmoplegia, ataxia and areflexia syndrome", "Guillain-Barre syndrome, Miller Fisher variant", "Ophthalmoplegia, Ataxia and Areflexia Syndrome", "Guillain Barre syndrome, Miller Fisher variant", "Guillain Barre Syndrome, Miller Fisher Variant", "Guillain-Barre Syndrome, Miller Fisher Variant", "Miller Fisher variant of Guillain Barre syndrome", "Miller-Fisher variant of Guillain-Barre syndrome", "Miller Fisher Variant of Guillain Barre Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Miller Fisher syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0022826", "names": ["congenital cystic eye multiple ocular and intracranial anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital cystic eye multiple ocular and intracranial anomalies", "shortest_name_length": 64}
{"curie": "MONDO:0014349", "names": ["PCH10", "pontocerebellar hypoplasia type 10", "Pontocerebellar hypoplasia type 10", "PONTOCEREBELLAR HYPOPLASIA, TYPE 10", "pontocerebellar hypoplasia, type 10", "CLP1-related pontocerebellar hypoplasia", "Congenital pontocerebellar hypoplasia type 10", "CLP1 non-syndromic pontocerebellar hypoplasia", "Congenital pontocerebellar hypoplasia type 10 (disorder)", "non-syndromic pontocerebellar hypoplasia caused by mutation in CLP1", "CLP1 (cleavage and polyadenylation factor I subunit 1) related pontocerebellar hypoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pontocerebellar hypoplasia type 10", "shortest_name_length": 5}
{"curie": "UMLS:C2347482", "names": ["Perinatal Brain Injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perinatal Brain Injury", "shortest_name_length": 22}
{"curie": "MONDO:0021925", "names": ["Tracheobronchitis", "tracheobronchitis", "TRACHEOBRONCHITIS", "Tracheobronchitis NOS", "tracheitis; bronchitis", "Tracheobronchitis, NOS", "Tracheobronchitis (disorder)", "tracheobronchitis (diagnosis)", "Bronchitis with tracheitis NOS", "Bronchitis NOS, with tracheitis NOS", "bronchitis; tracheitis (tracheobronchitis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tracheobronchitis", "shortest_name_length": 17}
{"curie": "MONDO:0016609", "names": ["IMAM", "imam", "inflammatory myopathy with abundant macrophages", "Inflammatory myopathy with abundant macrophages", "Inflammatory myopathy with abundant macrophages (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory myopathy with abundant macrophages", "shortest_name_length": 4}
{"curie": "UMLS:C4329998", "names": ["Focal KATP-Associated Hyperinsulinism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Focal KATP-Associated Hyperinsulinism", "shortest_name_length": 37}
{"curie": "MONDO:0008309", "names": ["primary release disorder of platelets", "Primary Release Disorder Of Platelets", "PRIMARY RELEASE DISORDER OF PLATELETS", "bleeding disorder due to primary defects in platelet release mechanism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary release disorder of platelets", "shortest_name_length": 37}
{"curie": "MONDO:0006652", "names": ["AMI", "ami", "almi", "Anterior MI", "anterior mi", "anterior infarction", "anterior heart attack", "Anterior myocardial infarction", "anterior myocardial infarction", "MYOCARDIAL INFARCTION ANTERIOR", "anteroseptal myocardial infarction", "infarction, anteroseptal myocardial", "MYOCARDIAL INFARCTION ANTEROLATERAL", "anterolateral myocardial infarction", "Anterior Wall Myocardial Infarction", "myocardial infarction, anteroseptal", "anteroseptal myocardial infarctions", "Anterolateral Myocardial Infarction", "Anterolateral myocardial infarction", "infarctions, anteroseptal myocardial", "myocardial infarction, anterior wall", "myocardial infarctions, anteroseptal", "anterolateral myocardial infarctions", "myocardial infarction, anterolateral", "anterior myocardial infarction (AMI)", "Infarction, Anterolateral Myocardial", "Myocardial Infarction, Anterior Wall", "Anterolateral Myocardial Infarctions", "infarction, anterolateral myocardial", "Myocardial Infarction, Anterolateral", "MYOCARDIAL INFARCTION (ANTERIOR WALL)", "infarctions, anterolateral myocardial", "Infarctions, Anterolateral Myocardial", "MYOCARDIAL INFARCTION (ANTEROLATERAL)", "Myocardial Infarctions, Anterolateral", "myocardial infarctions, anterolateral", "acute anterior wall myocardial infarction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anterolateral myocardial infarction", "shortest_name_length": 3}
{"curie": "UMLS:C1846386", "names": ["Focal Cortical Dysplasia of Taylor, Type IIa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Focal Cortical Dysplasia of Taylor, Type IIa", "shortest_name_length": 44}
{"curie": "UMLS:C0278472", "names": ["stage III adult HD", "adult HD, stage III", "HD, adult, stage III", "HD, stage III, adult", "Stage III Hodgkin Lymphoma", "Stage III Adult Hodgkin Lymphoma", "stage III adult Hodgkin lymphoma", "Adult Hodgkin's Disease Stage III", "stage III adult Hodgkin's disease", "Stage III Adult Hodgkin's Disease", "adult Hodgkin's disease, stage III", "Adult Hodgkin's Lymphoma Stage III", "Stage III Adult Hodgkin's Lymphoma", "lymphoma, stage III adult Hodgkin's", "Hodgkin's disease, stage III, adult", "Hodgkin's lymphoma, stage III, adult", "Ann Arbor Stage III Adult Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Adult Hodgkin Lymphoma", "shortest_name_length": 18}
{"curie": "MONDO:0024280", "names": ["Polyarthritis", "polyarthritis", "POLYARTHRITIS", "Polyarthritides", "polyarthritides", "Polyarthritis, NOS", "Polyarticular arthritis", "polyarticular arthritis", "Polyarticular Arthritis", "polyarthritis (diagnosis)", "POLYARTHRITIS INFLAMMATORY", "Polyarthritis, unspecified", "Inflammatory Polyarthritis", "inflammatory polyarthritis", "Inflammatory polyarthritis", "inflammatory; polyarthritis", "polyarthritis; inflammatory", "inflammatory polyarthropathy", "polyarthropathy inflammatory", "Inflammatory polyarthropathy", "Inflammatory polyarthropathies", "Inflammatory polyarthritis, NOS", "Inflammatory polyarthropathy, NOS", "ARTHRITIS, MULTIPLE JOINT INVOLVEMENT", "Inflammatory polyarthropathy (disorder)", "Inflammatory polyarthropathies (M05-M14)", "Inflammatory polyarthropathy (diagnosis)", "Unspecified inflammatory polyarthropathy", "Inflammatory arthritis of multiple joints", "Undifferentiated inflammatory polyarthritis", "Inflammatory polyarthropathy, site unspecified", "Inflammatory polyarthropathy or polyarthritis NOS", "Undifferentiated inflammatory polyarthritis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyarticular arthritis", "shortest_name_length": 13}
{"curie": "UMLS:C1333482", "names": ["Syncytial Endometritis", "Exaggerated placental site", "Exaggerated Placental Site", "Exaggerated placental site reaction", "Exaggerated Placental Site Reaction", "Exaggerated placental site (disorder)", "Exaggerated placental site (diagnosis)", "Exaggerated placental site (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Exaggerated placental site", "shortest_name_length": 22}
{"curie": "MONDO:0004605", "names": ["Callous ulcer", "callous ulcer", "Indolent ulcer", "indolent ulcer", "Chronic skin ulcer", "SKIN ULCER CHRONIC", "chronic skin ulcer", "Chronic ulcer skin", "Ulcer;skin;chronic", "chronic skin ulcers", "Chronic skin ulcers", "Chronic ulcer of skin", "chronic ulcer of skin", "chronic cutaneous ulcer", "Chronic ulcer of skin NOS", "Chronic ulcer of skin, NOS", "Chronic ulcer of skin (disorder)", "chronic cutaneous ulcer (diagnosis)", "Chronic skin ulcer of unspecified site", "Chronic ulcer of skin, unspecified site", "callous ulcer (morphologic abnormality)", "Chronic ulcer skin (including varicose)", "indolent ulcer (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic ulcer of skin", "shortest_name_length": 13}
{"curie": "MONDO:0020409", "names": ["univentricular heart with single atrio-ventricular valve"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "univentricular heart with single atrio-ventricular valve", "shortest_name_length": 56}
{"curie": "UMLS:C2350233", "names": ["Antley-Bixler Syndrome Phenotype", "Antley Bixler Syndrome Phenotype", "Phenotype, Antley-Bixler Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Antley-Bixler Syndrome Phenotype", "shortest_name_length": 32}
{"curie": "UMLS:C4744563", "names": ["Metastatic Lung Small Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Lung Small Cell Carcinoma", "shortest_name_length": 36}
{"curie": "UMLS:C1706727", "names": ["Adrenal Gland Angiosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adrenal Gland Angiosarcoma", "shortest_name_length": 26}
{"curie": "MONDO:0001498", "names": ["varicole", "Varicole", "varicoles", "varicocele", "VARICOCELE", "Varicocele", "varicocoele", "varicoceles", "Pampinocele", "Varicoceles", "Varicocoele", "scrotum; varix", "scrotal varices", "Scrotal varices", "varices; scrotum", "scrotal varicocele", "Vaginal varicocele", "Varicocele (disorder)", "scrotum varicose vein", "varicocele (diagnosis)", "scrotal varicose veins", "varicose veins scrotum", "Varicose veins;scrotum", "scrotum varicose veins", "Scrotal varicose veins", "scrotum varicose disease", "varicocele; spermatic cord", "spermatic cord; varicocele", "scrotal varices (diagnosis)", "varicose disease of scrotum", "Scrotal varices - varicocele", "varicocele (physical finding)", "varicose veins on the scrotum", "scrotal varicocele (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "varicocele", "shortest_name_length": 8}
{"curie": "UMLS:C2986682", "names": ["Loco-Regional", "Locoregional Recurrence", "Locally Recurrent Cancer", "locally recurrent cancer", "Locally Recurrent Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Recurrent Malignant Neoplasm", "shortest_name_length": 13}
{"curie": "UMLS:C4521827", "names": ["IIB", "Stage IIB Distal Bile Duct Cancer AJCC v8", "Stage IIB Distal Bile Duct Carcinoma AJCC v8", "Stage IIB Extrahepatic (Distal) Bile Duct Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Distal Bile Duct Cancer AJCC v8", "shortest_name_length": 3}
{"curie": "UMLS:C1336273", "names": ["Stage III Seminoma", "Stage III Testicular Seminoma", "Stage III Testicular Seminoma AJCC v6", "Stage III Testicular Seminoma AJCC v7", "Stage III Testicular Seminoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Testicular Seminoma AJCC v6 and v7", "shortest_name_length": 18}
{"curie": "UMLS:C5446649", "names": ["Recurrent Endometrial Adenosquamous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Endometrial Adenosquamous Carcinoma", "shortest_name_length": 45}
{"curie": "MONDO:0030063", "names": ["NEDSHBA", "neurodevelopmental disorder with seizures, hypotonia, and brain abnormalities", "neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities", "NEURODEVELOPMENTAL DISORDER WITH SEIZURES, HYPOTONIA, AND BRAIN IMAGING ABNORMALITIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities", "shortest_name_length": 7}
{"curie": "MONDO:0000944", "names": ["a.cerebri; occlusion", "Cerebral artery occlusion", "cerebral artery occlusion", "artery cerebral occlusion", "occlusion; cerebral artery", "Cerebral arterial occlusion", "occlusion; artery, cerebral", "Occlusion of cerebral artery", "Occlusion of cerebral arteries", "occlusion of cerebral arteries", "Cerebral artery occlusion, NOS", "Cerebral artery occlusion syndrome", "cerebral artery occlusion (diagnosis)", "Cerebral artery occlusion, unspecified", "Occlusion of cerebral artery (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral artery occlusion", "shortest_name_length": 20}
{"curie": "UMLS:C2044987", "names": ["CGIN", "Cervical Glandular Intraepithelial Neoplasia", "cervical intraepithelial glandular neoplasia", "intraepithelial glandular neoplasia of cervix", "intraepithelial glandular neoplasia of cervix (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intraepithelial glandular neoplasia of cervix", "shortest_name_length": 4}
{"curie": "MONDO:0016862", "names": ["ALGS1", "Alagille syndrome 1", "Alagille Syndrome 1", "ALAGILLE SYNDROME 1", "arteriohepatic dysplasia", "Alagille syndrome type 1", "Alagille-Watson syndrome", "hepatic ductular hypoplasia, syndromatic", "cholestasis with peripheral pulmonary stenosis", "Alagille syndrome due to a JAG1 point mutation", "arteriohepatic dysplasia due to a JAG1 point mutation", "Alagille-Watson syndrome due to a JAG1 point mutation", "syndromic bile duct paucity due to a JAG1 point mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alagille syndrome due to a JAG1 point mutation", "shortest_name_length": 5}
{"curie": "MONDO:0021232", "names": ["Pinealoma", "pinealoma", "pineal tumor", "Pineal Tumor", "pineal neoplasm", "Pineal Neoplasm", "Pineal neoplasms", "Pineal Area Tumor", "Pineal Body Tumor", "pineal area tumor", "pineal body tumor", "pineal region tumor", "Pineal Region Tumor", "pineal body neoplasm", "Pineal Area Neoplasm", "Tumor of Pineal Area", "pineal area neoplasm", "tumor of pineal area", "tumor of pineal body", "Pineal Body Neoplasm", "Pineal Region Neoplasm", "pineal region neoplasm", "tumor of pineal region", "Tumor of Pineal Region", "neoplasm of pineal area", "Neoplasm of Pineal Area", "neoplasm of pineal body", "Tumor of the Pineal Area", "tumor of the pineal area", "Neoplasm of Pineal Region", "neoplasm of pineal region", "tumor of the pineal region", "Tumor of the Pineal Region", "neoplasm of the pineal area", "Neoplasm of the Pineal Area", "Neoplasm of the Pineal Region", "neoplasm of the pineal region", "pineal body neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pineal body neoplasm", "shortest_name_length": 9}
{"curie": "MONDO:0015987", "names": ["APVR", "Halasz syndrome", "Scimitar Anomaly", "Scimitar anomaly", "SCIMITAR ANOMALY", "Scimitar Syndrome", "scimitar syndrome", "Anomaly, Scimitar", "Scimitar syndrome", "SCIMITAR SYNDROME", "syndrome; scimitar", "scimitar; syndrome", "hypogenetic lung syndrome", "Hypogenetic lung syndrome", "Scimitar syndrome (disorder)", "Pulmonary venolobar syndrome", "Scimitar syndrome (diagnosis)", "Pulmonary Venous Return Anomaly", "ANOMALOUS PULMONARY VENOUS RETURN", "Anomalous Pulmonary Venous Return", "Anomalous pulmonary venous return", "anomalous pulmonary venous return", "Congenital pulmonary venolobar syndrome", "congenital pulmonary venolobar syndrome", "Epibronchial right pulmonary vein syndrome", "anomalous pulmonary venous return (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scimitar syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0751081", "names": ["Trisomy 21, Mitotic Nondisjunction", "trisomy; 21, mitotic nondisjunction", "trisomy; syndrome, 21, mitotic nondisjunction", "syndrome; trisomy, 21, mitotic nondisjunction", "chromosome; 21, trisomy, mitotic nondisjunction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Trisomy 21, Mitotic Nondisjunction", "shortest_name_length": 34}
{"curie": "UMLS:C1336451", "names": ["Stage I Bone Sarcoma", "Stage I Sarcoma of Bone", "Stage I Sarcoma of the Bone", "Stage I Bone Sarcoma AJCC v7", "Stage I Bone Sarcoma  AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Bone Sarcoma AJCC v7", "shortest_name_length": 20}
{"curie": "MONDO:0004387", "names": ["luteoma", "Luteoma", "Luteomas", "Luteinoma", "luteinoma", "Luteoma NOS", "Luteoma, NOS", "LUTEOMA, BENIGN", "Luteal cell tumor", "Luteal Cell Tumor", "Luteal cell tumour", "Luteal Cell Neoplasm", "luteoma of pregnancy", "Leuteoma of Pregnancy", "leuteoma of pregnancy", "Ovarian Stroma Luteoma", "Ovarian Stromal Luteoma", "Luteoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "luteoma of pregnancy", "shortest_name_length": 7}
{"curie": "MONDO:0003026", "names": ["gallbladder angiosarcoma", "Gallbladder Angiosarcoma", "Gallbladder Hemangiosarcoma", "gallbladder hemangiosarcoma", "angiosarcoma of gallbladder", "Angiosarcoma of Gallbladder", "hemangiosarcoma of gallbladder", "Hemangiosarcoma of Gallbladder", "angiosarcoma of the gallbladder", "Angiosarcoma of the Gallbladder", "Hemangiosarcoma of the Gallbladder", "hemangiosarcoma of the gallbladder", "gall bladder angiosarcoma (disease)", "angiosarcoma (disease) of gall bladder", "angiosarcoma of gallbladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gallbladder angiosarcoma", "shortest_name_length": 24}
{"curie": "MONDO:0004866", "names": ["auditory tube disorder", "Auditory tube disorder", "eustachian tube disease", "eustachian tube disorder", "diseases eustachian tube", "Eustachian tube disorder", "Eustachian tube disorders", "tube disorders eustachian", "eustachian tube disorders", "disease of eustachian tube", "Dysfunction;eustachian tube", "EUSTACHIAN TUBE DYSFUNCTION", "Eustachian tube dysfunction", "disorder of eustachian tube", "eustachian tube dysfunction", "Disorder of Eustachian tube", "dysfunction eustachian tube", "Eustachian tube disorder NOS", "dysfunction eustachian tubes", "ET - Eustachian tube disorder", "pharyngotympanic tube disease", "Eustachian tube disorder, NOS", "eustachian tube disorder other", "Dysfunction of eustachian tube", "Dysfunction of Eustachian tube", "other eustachian tube disorder", "disease of pharyngotympanic tube", "DISORDERS OF THE EUSTACHIAN TUBE", "ETD - Eustachian tube dysfunction", "disorder of pharyngotympanic tube", "Other disorders of Eustachian tube", "Eustachian tube disorder (disorder)", "Unspecified Eustachian tube disorder", "Eustachian tube disorder, unspecified", "disease (or disorder); eustachian tube", "disorder of eustachian tube (diagnosis)", "eustachian tube dysfunction (diagnosis)", "Dysfunction of eustachian tube (disorder)", "pharyngotympanic tube disease or disorder", "other eustachian tube disorder (diagnosis)", "disease or disorder of pharyngotympanic tube", "Unspecified Eustachian tube disorder, unspecified ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eustachian tube disorder", "shortest_name_length": 22}
{"curie": "MONDO:0015624", "names": ["diazoxide-sensitive diffuse hyperinsulinism", "hyperinsulinemic hypoglycemia, diazoxide-sensitive diffuse form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diazoxide-sensitive diffuse hyperinsulinism", "shortest_name_length": 43}
{"curie": "MONDO:0010466", "names": ["DEE20", "MCAHS2", "EIEE20", "GPIBD4", "MCAHS type 2", "early infantile epileptic encephalopathy 20", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 20", "epileptic encephalopathy, early infantile, 20", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 20", "developmental and epileptic encephalopathy 20", "GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 4", "glycosylphosphatidylinositol biosynthesis defect 4", "multiple congenital anomalies-hypotonia-seizures syndrome 2", "MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2", "multiple congenital anomalies-hypotonia-seizures syndrome type 2", "PIGA multiple congenital anomalies/dysmorphic syndrome-intellectual disability", "multiple congenital anomalies-hypotonia-seizures syndrome 2, X-linked recessive", "multiple congenital anomalies/dysmorphic syndrome-intellectual disability caused by mutation in PIGA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple congenital anomalies-hypotonia-seizures syndrome 2", "shortest_name_length": 5}
{"curie": "UMLS:C4302111", "names": ["Familial Ménière disease", "Familial Ménière disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Familial Ménière disease", "shortest_name_length": 24}
{"curie": "MONDO:0011112", "names": ["WT5", "WTSL", "Wilms tumor 5", "WILMS TUMOR 5", "Wilms tumor type 5", "Wilms tumor, susceptibility to", "WILMS TUMOR, SUSCEPTIBILITY TO", "Wilms tumor and radial bilateral aplasia", "Bilateral radial aplasia with Wilms tumor", "bilateral radial aplasia with Wilms tumor", "Wilms tumor susceptibility-5, autosomal dominant, somatic mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wilms tumor 5", "shortest_name_length": 3}
{"curie": "MONDO:0012546", "names": ["Nphs3", "NPHS3", "PLCE1 nephrotic syndrome", "nephrotic syndrome type 3", "Nephrotic Syndrome, Type 3", "NEPHROTIC SYNDROME, TYPE 3", "nephrotic syndrome, type 3", "early onset nephrotic syndrome type 3", "NEPHROTIC SYNDROME, EARLY-ONSET, TYPE 3", "nephrotic syndrome, early-onset, type 3", "Nephrotic Syndrome, Early-Onset, Type 3", "nephrotic syndrome caused by mutation in PLCE1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrotic syndrome, type 3", "shortest_name_length": 5}
{"curie": "MONDO:0004145", "names": ["Syncytial meningioma", "meningioma; syncytial", "syncytial; meningioma", "meningothelial meningioma", "Meningothelial Meningioma", "Meningothelial meningioma", "Endotheliomatous meningioma", "meningioma; endotheliomatous", "endotheliomatous; meningioma", "Meningotheliomatous meningioma", "Meningotheliomatous Meningioma", "Meningotheliomatous Meningiomas", "meningotheliomatous; meningioma", "Meningioma, Meningotheliomatous", "meningioma; meningotheliomatous", "Meningiomas, Meningotheliomatous", "meningothelial meningioma (morphologic abnormality)", "Meningothelial meningioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "meningothelial meningioma", "shortest_name_length": 20}
{"curie": "MONDO:0005408", "names": ["diabetes mellitus type 2 associated cataract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diabetes mellitus type 2 associated cataract", "shortest_name_length": 44}
{"curie": "UMLS:C0345237", "names": ["Short Segment Hirschsprung Disease", "Short segment Hirschsprung disease", "Short Segment Hirschsprung's Disease", "Short segment Hirschsprung's disease", "Short segment Hirschsprung's disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Short segment Hirschsprung's disease", "shortest_name_length": 34}
{"curie": "UMLS:C3278252", "names": ["Red Cell Adenylate Kinase Deficiency", "Red cell adenylate kinase deficiency", "Erythrocyte Adenylate Kinase Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Red cell adenylate kinase deficiency", "shortest_name_length": 36}
{"curie": "UMLS:C0750910", "names": ["Pre Ictal Memory Loss", "Pre-Ictal Memory Loss", "Memory Loss, Pre-Ictal", "Pre-Ictal Memory Losses", "Memory Losses, Pre-Ictal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pre-Ictal Memory Loss", "shortest_name_length": 21}
{"curie": "MONDO:0002448", "names": ["Larynx Sarcoma", "larynx sarcoma", "sarcoma of larynx", "Sarcoma of Larynx", "laryngeal sarcoma", "Laryngeal Sarcoma", "sarcoma of the larynx", "Sarcoma of the Larynx", "sarcoma of larynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laryngeal sarcoma", "shortest_name_length": 14}
{"curie": "MONDO:0800129", "names": ["SAIDX", "NEMO deleted exon 5 syndrome", "autoinflammatory disease, X-linked", "autoinflammatory syndrome, X-linked", "AUTOINFLAMMATORY DISEASE, SYSTEMIC, X-LINKED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoinflammatory disease, X-linked", "shortest_name_length": 5}
{"curie": "UMLS:C0220647", "names": ["CUP", "cancer of unknown origin", "unknown primary carcinoma", "CARCINOMA PRIMARY UNKNOWN", "carcinoma of unknown primary", "Carcinoma of unknown primary", "Carcinoma of Unknown Primary", "Cancer of unknown primary origin", "carcinoma of unknown primary (CUP)", "Carcinoma of Unknown Primary Origin", "METASTATIC CARCINOMA WITH UNKNOWN PRIMARY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carcinoma of unknown primary", "shortest_name_length": 3}
{"curie": "MONDO:0014535", "names": ["HYPERPROINSULINEMIA", "Hyperproinsulinemia", "hyperproinsulinemia", "Hyperproinsulinaemia", "Hyperproinsulinemia (disorder)", "Hyperproinsulinemia (diagnosis)", "diabetes mellitus hyperproinsulinemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperproinsulinemia", "shortest_name_length": 19}
{"curie": "MONDO:0001600", "names": ["RANULA", "Ranula", "ranula", "ranulas", "Ranulas", "Sialocele", "sialocele", "Ptyalocele", "salivary cyst", "Salivary Cyst", "Salivary cyst", "cysts salivary", "Sublingual cyst", "sublingual cyst", "Cyst, sublingual", "cysts sublingual", "Ranula (disorder)", "Salivary mucocele", "ranula (diagnosis)", "Sublingual mucocele", "Sublingual ptyalocele", "salivary gland mucocele", "Salivary gland mucocele", "Salivary gland mucocoele", "Mucocoele;salivary gland", "mucocele; salivary gland", "salivary gland mucocoele", "salivary gland; mucocele", "Ranula of floor of mouth", "Mucocele of salivary gland", "mucocele of salivary gland", "Mucocoele of salivary gland", "Retention cyst of salivary gland", "Mucocele of salivary gland (disorder)", "mucocele of salivary gland (diagnosis)", "mucous retention cyst of salivary gland", "Mucous retention cyst of salivary gland", "Ranula of salivary gland of floor of mouth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucocele of salivary gland", "shortest_name_length": 6}
{"curie": "MONDO:0020214", "names": ["Posterior corneal dystrophy", "posterior corneal dystrophy", "Dystrophy of posterior cornea", "posterior corneal dystrophy (diagnosis)", "Dystrophy of posterior cornea (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "posterior corneal dystrophy", "shortest_name_length": 27}
{"curie": "UMLS:C0280347", "names": ["Stage I Mouth Adenoid Cystic Carcinoma", "Stage I Adenoid Cystic Carcinoma of Mouth", "Stage I Oral Cavity Adenoid Cystic Cancer", "Stage I Oral Cavity Adenoid Cystic Carcinoma", "Stage I Adenoid Cystic Carcinoma of the Mouth", "oral cavity adenoid cystic carcinoma, stage I", "Stage I Adenoid Cystic Carcinoma of Oral Cavity", "stage I adenoid cystic carcinoma of the oral cavity", "Stage I Adenoid Cystic Carcinoma of the Oral Cavity", "Adenoid cystic carcinoma of the oral cavity stage I", "Stage I Oral Cavity Adenoid Cystic Carcinoma AJCC v6", "adenoid cystic carcinoma of the oral cavity, stage I", "Stage I Oral Cavity Adenoid Cystic Carcinoma AJCC v7", "Stage I Oral Cavity Adenoid Cystic Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenoid cystic carcinoma of the oral cavity stage I", "shortest_name_length": 38}
{"curie": "UMLS:C2827598", "names": ["XXXY and XXXXY Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "XXXY and XXXXY Syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0035646", "names": ["Congenital-onset Steinert disease", "Congenital-onset myotonic dystrophy type 1", "congenital-onset Steinert myotonic dystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital-onset Steinert myotonic dystrophy", "shortest_name_length": 33}
{"curie": "MONDO:0002413", "names": ["GSD1", "GSD I", "GSD type 1", "Von Gierke", "GSD type I", "G6P deficiency", "Glycogenosis 1", "Gierke Disease", "Gierkes Disease", "Disease, Gierke", "Gierke's Disease", "gierke's disease", "Disease, Gierke's", "VON GIERKE DISEASE", "von Gierke disease", "von Gierke Disease", "Von Gierke disease", "von gierke disease", "Disease, von Gierke", "von gierkes disease", "von Gierkes Disease", "Glycogenosis type I", "Glycogenosis type 1", "glycogenosis type i", "glycogenosis type I", "glycogenosis type 1", "von Gierke's disease", "von Gierke's Disease", "GLYCOGENOSIS, TYPE I", "Von Gierke's disease", "von gierke's disease", "Disease, von Gierke's", "diseases gierke's von", "Liver glycogen disease", "Van Creveld-von Gierke", "Hepatorenal glycogenosis", "hepatorenal glycogenosis", "HEPATORENAL GLYCOGENOSIS", "GSD due to G6P deficiency", "GLYCOGENOSIS, HEPATORENAL", "glycogen storage disease I", "i glycogen storage disease", "Glycogen storage disease 1", "glycogen storage disease i", "glycogen storage disease Ia", "Glucosephosphatase Deficiency", "Deficiency, Glucosephosphatase", "Type I glycogen storage disease", "Glycogen Storage Disease Type I", "glycogen storage disease type I", "disease glycogen i storage type", "Glucosephosphatase Deficiencies", "glycogen storage disease type i", "Glycogen storage disease type I", "Glycogen storage disease type 1", "glycogen storage disease type 1", "GLYCOGEN STORAGE DISEASE TYPE I", "type i glycogen storage disease", "Glycogen storage disease type Ia", "glycogen storage disease, type I", "Glucose-6-Phosphatase Deficiency", "glucose-6-phosphatase deficiency", "Glycogen storage disease, type I", "Glycogen storage disease, type 1", "Glucose 6 Phosphatase Deficiency", "Deficiencies, Glucosephosphatase", "GLUCOSE 6 PHOSPHATASE DEFICIENCY", "Glucose-6-phosphatase deficiency", "glucose 6 phosphatase deficiency", "von Gierke's disease (GSD type I)", "Deficiency, Glucose-6-Phosphatase", "glucose-6-phosphatase; deficiency", "deficiency; glucose-6-phosphatase", "Glucose-6-Phosphatase Deficiencies", "Glycogen Storage Disease 1 (GSD I)", "Deficiency of glucose-6-phosphatase", "Deficiencies, Glucose-6-Phosphatase", "deficiency of glucose-6-phosphatase", "Hepatorenal Glycogen Storage Disease", "Hepatorenal glycogen storage disease", "hepatorenal glycogen storage disease", "glycogen storage; disease, hepatorenal", "Glycogen storage disease, type I (disorder)", "glucose-6-phosphatase deficiency (diagnosis)", "von Gierke's disease (GSD type I) (diagnosis)", "Deficiency of glucose-6-phosphatase (disorder)", "Glycogen storage disease due to G6P deficiency", "glycogen storage disease due to G6P deficiency", "Glycogen storage disease due to glucose-6-phosphatase deficiency", "glycogen storage disease due to glucose-6-phosphatase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease I", "shortest_name_length": 4}
{"curie": "UMLS:C0475739", "names": ["Perinatal Subependymal Hemorrhage with Intraventricular and Intracerebral Extension", "Perinatal subependymal hemorrhage with intraventricular and intracerebral extension", "Perinatal subependymal haemorrhage with intraventricular and intracerebral extension", "Perinatal subependymal hemorrhage with intraventricular and intracerebral extension (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perinatal subependymal hemorrhage with intraventricular and intracerebral extension", "shortest_name_length": 83}
{"curie": "MONDO:0011604", "names": ["SOS", "SPONDYLOOCULAR SYNDROME", "Spondyloocular syndrome", "spondyloocular syndrome", "spondylo-ocular syndrome", "Spondylo-ocular syndrome", "Spondyloocular syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondylo-ocular syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C0751508", "names": ["Long sleeper syndrome", "Long Sleeper Syndrome", "Long Sleeper Syndromes", "Sleeper Syndrome, Long", "Syndrome, Long Sleeper", "Sleeper Syndromes, Long", "Syndromes, Long Sleeper", "Long sleeper syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Long Sleeper Syndrome", "shortest_name_length": 21}
{"curie": "MONDO:0016642", "names": ["meningioma", "Meningioma", "Meningiomas", "Meningioma, NOS", "brain meningioma", "Cranial meningioma", "cranial meningioma", "meningeal neoplasm", "Meningioma of brain", "meningioma of brain", "meningioma (disease)", "intracranial meningioma", "Intracranial Meningioma", "Intracranial meningioma", "primary Meningeal tumor", "primary meningeal tumor", "Meningioma, Intracranial", "Intracranial Meningiomas", "neoplasm of the meninges", "Meningiomas, Intracranial", "meningothelial cell tumor", "supratentorial meningioma", "Intracranial meningioma (disorder)", "Intracranial meningioma (diagnosis)", "meningeal neoplasm intracranial meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "meningioma", "shortest_name_length": 10}
{"curie": "UMLS:C5554910", "names": ["Locally Advanced Microsatellite Stable Colon Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Microsatellite Stable Colon Carcinoma", "shortest_name_length": 54}
{"curie": "MONDO:0000741", "names": ["perleche", "Perleche", "Perlèche", "PERLECHE", "perlèche", "CHEILOSIS", "Cheilosis", "cheilosis", "cheilosis of lip", "angular cheilosis", "angular cheilitis", "Angular Cheilitis", "Angular cheilitis", "Angular cheilosis", "Angular stomatitis", "angular stomatitis", "STOMATITIS ANGULAR", "stomatitis angular", "Cheilitis, angular", "stomatitis; angular", "angular; stomatitis", "angulus infectiosus", "Intertrigo labialis", "perleche (diagnosis)", "Cheilosis (disorder)", "commissural cheilitis", "Commissural cheilitis", "cheilosis of lip (diagnosis)", "Angular cheilitis (disorder)", "angular cheilitis (diagnosis)", "Inflammation of oral commisures", "angle of oral opening cheilitis", "Red and sore corners of the mouth", "cheilitis of angle of oral opening", "cheilosis of lip (physical finding)", "Inflammation of corners of the mouth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angular cheilitis", "shortest_name_length": 8}
{"curie": "MONDO:0002334", "names": ["Blood tumor", "blood tumor", "cancer blood", "Blood cancer", "Blood tumour", "blood cancer", "Blood Cancer", "Cancer, Blood", "blood cancers", "Blood Cancers", "tumor of blood", "Carcinoma;blood", "neoplasm of blood", "Hematologic Cancer", "Hematologic cancer", "hematologic cancer", "Hematopoietic Tumor", "Hematological Tumor", "hematological tumors", "Hematopoietic Cancer", "hematologic neoplasm", "Hematologic Neoplasm", "Hematologic neoplasm", "Hematopoietic Tumors", "hematopoietic cancer", "hematopoietic tumors", "Hematological Tumors", "HEMATOPOIETIC CANCER", "Hematological tumors", "Hematologic Neoplasms", "bone marrow carcinoma", "Neoplasm, Hematologic", "Haematologic neoplasm", "carcinoma bone marrow", "hematologic neoplasms", "Carcinoma;bone;marrow", "bone carcinoma marrow", "Hematopoietic Neoplasm", "Hematopoietic neoplasm", "Hematologic malignancy", "Hematological Neoplasm", "hematopoietic neoplasm", "Hematologic Malignancy", "hematologic malignancy", "Neoplasms, Hematologic", "Hematological neoplasm", "Neoplasm, Hematological", "neoplasms hematopoietic", "Haematological neoplasm", "Hematopoietic Neoplasms", "Hematological Neoplasms", "Neoplasm, Hematopoietic", "Haematologic malignancy", "Haematopoietic neoplasm", "Malignancy, Hematologic", "blood neoplasm (disease)", "hematologic malignancies", "Hematopoietic Malignancy", "Hematological Malignancy", "Hematological malignancy", "malignancies hematologic", "hematopoietic malignancy", "Hematopoietic Cell Tumor", "hematological malignancy", "Neoplasms, Hematopoietic", "Hematologic Malignancies", "haematological malignancy", "Malignancies, Hematologic", "Malignancy, Hematopoietic", "Haematological malignancy", "Malignancy, Hematological", "hematopoietic system tumor", "Hematological Malignancies", "hematological malignancies", "Hematopoietic Malignancies", "Hematopoietic neoplasm NOS", "Haematopoietic neoplasm NOS", "tumor of hematopoietic system", "hematopoietic/lymphoid cancer", "hematopoietic system neoplasm", "Malignant Hematologic Neoplasm", "Hematologic neoplasm (disorder)", "Malignant hematopoietic neoplasm", "malignant hematopoietic neoplasm", "Malignant Hematopoietic Neoplasm", "Hematopoietic, Including Myeloma", "neoplasm of hematopoietic system", "Malignant haematopoietic neoplasm", "Hematopoietic and Lymphoid Neoplasm", "Hematopoietic and Lymphoid Neoplasms", "Hematopoietic and Lymphoid System Tumor", "hematopoietic and lymphoid system tumor", "Hematopoietic and Lymphoid Cell Neoplasm", "Hematopoietic and Lymphoid System Neoplasm", "hematopoietic and lymphoid system neoplasm", "Hematopoietic Neoplasms including Lymphomas", "Hematopoietic Neoplasms Including Lymphomas", "Cancer of lymphatic and hematopoietic tissue", "Hematopoietic neoplasm (morphologic abnormality)", "hematopoietic neoplasm (morphologic abnormality)", "Malignant neoplasm of lymphatic and hemopoietic tissue", "Malignant neoplasm of lymphatic and haemopoietic tissue", "MALIGNANT NEOPLASM OF LYMPHATIC AND HEMATOPOIETIC TISSUE", "malignant hematopoietic neoplasm (morphologic abnormality)", "Malignant hematopoietic neoplasm (morphologic abnormality)", "Malignant tumor of lymphoid hemopoietic and related tissue", "Malignant tumour of lymphoid haemopoietic and related tissue", "Malignant tumor of lymphoid, hemopoietic AND/OR related tissue", "Malignant neoplasms of lymphoid, hematopoietic and related tissue", "malignant neoplasm of lymphoid, hemopoietic and/or related tissue", "Malignant neoplasms of lymphoid, haematopoietic and related tissue", "Malignant tumor of lymphoid, hemopoietic AND/OR related tissue (disorder)", "Malignant neoplasms of lymphoid, hematopoietic and related tissue (C81-C96)", "malignant neoplasm of lymphoid, hemopoietic and/or related tissue (diagnosis)", "Malignant neoplasm of lymphoid, hematopoietic and related tissue, unspecified", "Malignant neoplasm of lymphoid, haematopoietic and related tissue, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hematopoietic and lymphoid system neoplasm", "shortest_name_length": 11}
{"curie": "MONDO:0004316", "names": ["Skin Adenoid Squamous Cell Carcinoma", "Acantholytic squamous cell carcinoma", "Acantholytic Squamous Cell Skin Carcinoma", "Skin Acantholytic Squamous Cell Carcinoma", "acantholytic squamous cell skin carcinoma", "Acantholytic Squamous Cell Carcinoma of Skin", "Acantholytic squamous cell carcinoma of skin", "Skin Pseudoglandular Squamous Cell Carcinoma", "acantholytic squamous cell carcinoma of skin", "acantholytic squamous cell carcinoma of the skin", "Acantholytic Squamous Cell Carcinoma of the Skin", "SCC - Acantholytic squamous cell carcinoma of skin", "skin neoplasm carcinoma squamous cell acantholytic", "Acantholytic squamous cell carcinoma of skin (disorder)", "Acantholytic squamous cell carcinoma of skin (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acantholytic squamous cell skin carcinoma", "shortest_name_length": 36}
{"curie": "UMLS:C5419072", "names": ["Locally Advanced Cutaneous Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Cutaneous Melanoma", "shortest_name_length": 35}
{"curie": "MONDO:0033304", "names": ["DFNY", "Y-linked deafness", "nonsyndromic deafness, Y-linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nonsyndromic deafness, Y-linked", "shortest_name_length": 4}
{"curie": "MONDO:0013562", "names": ["susceptibility to aspergillosis", "aspergillosis, susceptibility to", "ASPERGILLOSIS, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aspergillosis, susceptibility to", "shortest_name_length": 31}
{"curie": "MONDO:0009228", "names": ["gingival fibromatosis with distinctive facies", "FIBROMATOSIS, GINGIVAL, WITH DISTINCTIVE FACIES", "Fibromatosis, Gingival, with Distinctive Facies", "fibromatosis, gingival, with distinctive facies", "gingival fibromatosis-facial dysmorphism syndrome", "gingival fibromatosis with craniofacial dysmorphism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gingival fibromatosis-facial dysmorphism syndrome", "shortest_name_length": 45}
{"curie": "MONDO:0007165", "names": ["SPAX7", "spastic ataxia 7", "spastic ataxia type 7", "SPASTIC ATAXIA 7, AUTOSOMAL DOMINANT", "spastic ataxia 7, autosomal dominant", "spastic ataxia with congenital miosis", "Spastic ataxia with congenital miosis", "SPASTIC ATAXIA WITH CONGENITAL MIOSIS", "Ataxia, Spastic, with Congenital Miosis", "MIOSIS, CONGENITAL, WITH SPASTIC ATAXIA", "miosis, congenital, with spastic ataxia", "Miosis, Congenital, with Spastic Ataxia", "Autosomal dominant spastic ataxia type 7", "autosomal dominant spastic ataxia type 7", "Spastic ataxia with congenital miosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic ataxia 7", "shortest_name_length": 5}
{"curie": "MONDO:0016899", "names": ["Duchenne and Becker muscular dystrophy", "severe dystrophinopathy, Duchenne and Becker type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Duchenne and Becker muscular dystrophy", "shortest_name_length": 38}
{"curie": "UMLS:C1096393", "names": ["Body fat disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Body fat disorder", "shortest_name_length": 17}
{"curie": "MONDO:0001548", "names": ["Coma;hepatic", "HEPATIC COMA", "Coma hepatic", "coma hepatic", "Hepatic Coma", "COMA HEPATIC", "Hepatic coma", "hepatic coma", "Hepatic Comas", "coma; hepatic", "COMA, HEPATIC", "Coma, Hepatic", "hepatic; coma", "Comas, Hepatic", "Hepatic coma NOS", "Hepatic coma (disorder)", "Hepatocerebral intoxication", "hepatocerebral intoxication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatic coma", "shortest_name_length": 12}
{"curie": "MONDO:0004355", "names": ["Leukemia", "leukemia", "childhood leukemia", "Childhood Leukemia", "Leukemia, Childhood", "Leukemia in children", "pediatric leukemia (disease)", "childhood leukemia (disease)", "leukemia (disease) of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood leukemia", "shortest_name_length": 8}
{"curie": "MONDO:0022742", "names": ["industrial asthma", "asthma industrial", "Industrial asthma", "Occupational asthma", "asthma occupational", "Occupational Asthma", "occupational asthma", "Asthma, Occupational", "Occupational Asthmas", "Asthmas, Occupational", "Occupational asthma (disorder)", "occupational asthma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "occupational asthma", "shortest_name_length": 17}
{"curie": "MONDO:0030341", "names": ["CMS7B", "myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive", "MYASTHENIC SYNDROME, CONGENITAL, 7B, PRESYNAPTIC, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive", "shortest_name_length": 5}
{"curie": "MONDO:0012956", "names": ["MS2", "MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO, 2", "multiple sclerosis, susceptibility to, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple sclerosis, susceptibility to, 2", "shortest_name_length": 3}
{"curie": "MONDO:0010568", "names": ["AIC", "AICARDI SYNDROME", "Aicardi Syndrome", "Aicardi syndrome", "aicardi syndrome", "Syndrome, Aicardi", "Aicardi's syndrome", "aicardi's syndrome", "Aicardi's Syndrome", "Syndrome, Aicardi's", "AIC - Aicardi syndrome", "Aicardi's syndrome (disorder)", "Chorioretinal Anomalies with Acc", "Aicardi syndrome, X-linked dominant", "Callosal Agenesis and Ocular Abnormalities", "Microphthalmia, seizure, hypsarrhythmia syndrome", "corpus callosum agenesis of with chorioretinal abnormality", "Agenesis of corpus callosum with chorioretinal abnormality", "agenesis of corpus callosum with chorioretinal abnormality", "Agenesis of Corpus Callosum with Chorioretinal Abnormality", "corpus callosum agenesis-chorioretinal abnormality syndrome", "corpus callosum, agenesis of, with chorioretinal Abnormality", "CORPUS CALLOSUM, AGENESIS OF, WITH CHORIORETINAL ABNORMALITY", "Corpus Callosum, Agenesis Of, With Chorioretinal Abnormality", "corpus callosum agenesis-ocular anomalies-salaam seizures syndrome", "corpus callosum agenesis-chorioretinopathy-infantile spasms syndrome", "chorioretinal anomalies-corpus callosum agenesis-infantile spasms syndrome", "Agenesis of Corpus Callosum with Infantile Spasms and Ocular Abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aicardi syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C5205889", "names": ["PERSISTENT HYALOID VESSELS", "Persistent Hyaloid Vessels"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Persistent Hyaloid Vessels", "shortest_name_length": 26}
{"curie": "UMLS:C1513716", "names": ["Ovarian Mucinous Cystic Tumor with Mural Nodules"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Mucinous Cystic Tumor with Mural Nodules", "shortest_name_length": 48}
{"curie": "MONDO:0013029", "names": ["SCA9", "SPINOCEREBELLAR ATAXIA 9", "cerebellar ataxia type 9", "spinocerebellar ataxia 9", "spinocerebellar ataxia type 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellar ataxia type 9", "shortest_name_length": 4}
{"curie": "MONDO:0013921", "names": ["IIAE6", "TICAM1 herpes simplex encephalitis", "herpes simplex encephalitis, susceptibility to, 4", "HERPES SIMPLEX ENCEPHALITIS, SUSCEPTIBILITY TO, 4", "Herpes simplex encephalitis, susceptibility to, type 4", "herpes simplex encephalitis caused by mutation in TICAM1", "encephalopathy, acute, infection-induced, susceptibility to, 6", "encephalopathy, acute, infection-induced (HERPES-specific), susceptibility to, 6", "ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 6", "encephalopathy, acute, infection-induced (Herpes-specific), susceptibility to, 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "herpes simplex encephalitis, susceptibility to, 4", "shortest_name_length": 5}
{"curie": "MONDO:0006203", "names": ["squamous cell bile duct carcinoma", "bile duct squamous cell carcinoma", "Squamous Cell Bile Duct Carcinoma", "Bile Duct Squamous Cell Carcinoma", "Squamous Cell Carcinoma of Bile Duct", "squamous cell carcinoma of bile duct", "squamous cell carcinoma of the bile duct", "Squamous Cell Carcinoma of the Bile Duct", "Extrahepatic Bile Duct Squamous Cell Carcinoma", "extrahepatic bile duct squamous cell carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extrahepatic bile duct squamous cell carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0011250", "names": ["microcephaly, macrotia, and mental retardation", "Microcephaly, Macrotia, And Mental Retardation", "MICROCEPHALY, MACROTIA, AND MENTAL RETARDATION", "microcephaly, macrotia, and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly, macrotia, and intellectual disability", "shortest_name_length": 46}
{"curie": "MONDO:0021977", "names": ["basaloid follicular hamartoma", "Basaloid follicular hamartoma", "basal cell nevus with comedones", "Basal Cell Nevus with Comedones", "Basal cell nevus with comedones", "Basal cell naevus with comedones", "Basal cell nevus with comedones (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "basaloid follicular hamartoma", "shortest_name_length": 29}
{"curie": "UMLS:C2109308", "names": ["Keratinizing squamous cell carcinoma", "Lung Keratinizing Squamous Cell Carcinoma", "Keratinizing Squamous Cell Lung Carcinoma", "keratinizing squamous cell carcinoma of lung", "keratinizing squamous cell carcinoma of lung (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratinizing squamous cell carcinoma of lung", "shortest_name_length": 36}
{"curie": "MONDO:0006395", "names": ["rectal Villotubular adenoma", "Rectal Villotubular Adenoma", "rectal tubulovillous adenoma", "Rectal Tubulovillous Adenoma", "Villotubular Adenoma of Rectum", "Villotubular adenoma of rectum", "Tubulovillous Adenoma of Rectum", "Tubulovillous adenoma of rectum", "tubulovillous adenoma of rectum", "Villotubular adenoma of the rectum", "Villotubular Adenoma of the Rectum", "tubulovillous adenoma of the rectum", "Tubulovillous Adenoma of the Rectum", "Tubulovillous adenoma of rectum (disorder)", "tubulovillous adenoma of rectum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rectal tubulovillous adenoma", "shortest_name_length": 27}
{"curie": "UMLS:C1096256", "names": ["Cryptococcal cutaneous infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cryptococcal cutaneous infection", "shortest_name_length": 32}
{"curie": "UMLS:C5203125", "names": ["Metastatic Biliary Tract Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Biliary Tract Carcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0013815", "names": ["BBDS", "BBDS1", "bent bone dysplasia syndrome", "BENT BONE DYSPLASIA SYNDROME", "bent bone dysplasia syndrome 1", "BENT BONE DYSPLASIA SYNDROME 1", "FGFR2-related bent bone dysplasia", "bent bone dysplasia (BBD)-FGFR2 type", "perinatal lethal bent bone dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bent bone dysplasia syndrome 1", "shortest_name_length": 4}
{"curie": "MONDO:0002943", "names": ["basal cell external ear carcinoma", "external Ear basal cell carcinoma", "external ear basal cell carcinoma", "External Ear Basal Cell Carcinoma", "Basal Cell Carcinoma of External Ear", "basal cell carcinoma of external Ear", "basal cell carcinoma of external ear", "external ear skin basal cell carcinoma", "Basal cell carcinoma of the External ear", "basal cell carcinoma of the external ear", "Basal Cell Carcinoma of the External Ear", "basal cell carcinoma of the external Ear", "skin basal cell carcinoma of external ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "external ear basal cell carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0011470", "names": ["FCHL2", "hyplip2", "HYPLIP2", "hyperlipidemia, combined, 2", "Hyperlipidemia, Combined, 2", "HYPERLIPIDEMIA, COMBINED, 2", "hyperlipidemia, combined, type 2", "Hyperlipidemia, Familial Combined, 2", "HYPERLIPIDEMIA, FAMILIAL COMBINED, 2", "hyperlipidemia, familial combined, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperlipidemia, combined, 2", "shortest_name_length": 5}
{"curie": "MONDO:0007899", "names": ["LSA", "Lichen Sclerosus", "Lichen Scleroses", "sclerosus lichen", "Lichen Sclerosis", "lichen sclerosis", "Lichen sclerosus", "lichen sclerosus", "lichens sclerosus", "lichen; sclerosus", "Sclerosus, Lichen", "Scleroses, Lichen", "Sclerosis, Lichen", "sclerosus; lichen", "White spot disease", "white spot disease", "white spot; disease", "disease; white spot", "Lichen sclerosus (disorder)", "lichen sclerosis atrophicus", "Lichen sclerosis atrophicus", "atrophicus lichens sclerosis", "lichen sclerosis et atrophicus", "lichen SCLEROSUS ET ATROPHICUS", "lichen et sclerosus atrophicus", "Lichen sclerosus et atrophicus", "Lichen Sclerosus et Atrophicus", "lichen et atrophicus sclerosus", "LICHEN SCLEROSUS ET ATROPHICUS", "Lichen Sclerosis et Atrophicus", "lichen sclerosus et atrophicus", "Lichen sclerosus et atrophicus, NOS", "lichen sclerosus et atrophicus (diagnosis)", "white spot; lichen sclerosus et atrophicus", "Lichen sclerosus (morphologic abnormality)", "disease (or disorder); white spot (lichen sclerosus et atrophicus)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lichen sclerosus et atrophicus", "shortest_name_length": 3}
{"curie": "MONDO:0016156", "names": ["qualitative or quantitative defects of FKRP"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of FKRP", "shortest_name_length": 43}
{"curie": "MONDO:0022071", "names": ["carbon baby syndrome", "Universal acquired melanosis", "universal acquired melanosis", "Universal acquired melanosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carbon baby syndrome", "shortest_name_length": 20}
{"curie": "UMLS:C4055190", "names": ["Toxoplasma Associated Congenital Nephrotic Syndrome", "Congenital Nephrotic Syndrome - Toxoplasma Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Nephrotic Syndrome - Toxoplasma Associated", "shortest_name_length": 51}
{"curie": "UMLS:C3898462", "names": ["Masaoka Stage IV", "Masaoka-Koga Stage IV"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Masaoka-Koga Stage IV", "shortest_name_length": 16}
{"curie": "MONDO:0044348", "names": ["hemoglobinopathy", "globin abnormality", "hemoglobin disease", "hemoglobin disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemoglobinopathy", "shortest_name_length": 16}
{"curie": "UMLS:C0340855", "names": ["Micturition Syncope", "micturition syncope", "SYNCOPE MICTURITION", "Micturition syncope", "Syncope micturition", "Micturition Syncopes", "Syncope, Micturition", "Syncopes, Micturition", "Micturition syncope (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Syncope, Micturition", "shortest_name_length": 19}
{"curie": "UMLS:C1333978", "names": ["Liver Cancer Secondary to Hepatitis C", "Hepatitis C Virus Related Hepatocellular Carcinoma", "Hepatitis C Virus-Related Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatitis C Virus-Related Hepatocellular Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0017964", "names": ["46,XX DSD induced by exogenous maternal-derived androgen", "46,XX disorder of sex development induced by exogenous maternal-derived androgen"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XX disorder of sex development induced by exogenous maternal-derived androgen", "shortest_name_length": 56}
{"curie": "MONDO:0010876", "names": ["Recessive aplasia cutis congenita of limbs", "recessive aplasia cutis congenita of limbs", "aplasia cutis congenita of limbs recessive", "Aplasia cutis congenita of limbs recessive", "Aplasia Cutis Congenita of Limbs, Recessive", "recessive aplasia cutis congenita of the limbs", "Recessive aplasia cutis congenita of the limbs", "Autosomal recessive aplasia cutis congenita of limb", "aplasia cutis congenita of limbs, autosomal recessive", "APLASIA CUTIS CONGENITA OF LIMBS, AUTOSOMAL RECESSIVE", "congenital absence of skin on the upper or lower limbs", "Congenital absence of skin on the upper or lower limbs", "Autosomal recessive aplasia cutis congenita of limb (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "recessive aplasia cutis congenita of limbs", "shortest_name_length": 42}
{"curie": "MONDO:0008003", "names": ["PEOA1", "adPEO", "autosomal dominant progressive external ophthalmoplegia", "progressive external ophthalmoplegia, autosomal dominant", "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1", "Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1", "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant progressive external ophthalmoplegia", "shortest_name_length": 5}
{"curie": "MONDO:0013798", "names": ["chromosome 16q22 deletion syndrome", "CHROMOSOME 16q22 DELETION SYNDROME", "chromosome 16q22 deletion syndrome, isolated cases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 16q22 deletion syndrome", "shortest_name_length": 34}
{"curie": "MONDO:0032895", "names": ["DEE83", "EIEE83", "BARAKAT-PERENTHALER SYNDROME", "Barakat-Perenthaler Syndrome", "early infantile epileptic encephalopathy 83", "developmental and epileptic encephalopathy 83", "epileptic encephalopathy, early infantile, 83", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 83", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 83", "developmental and epileptic encephalopathy, 83"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 83", "shortest_name_length": 5}
{"curie": "MONDO:0004169", "names": ["pmt", "PREMENSTRUAL TENSION", "premenstrual tension", "Premenstrual tension", "Premenstrual Tension", "Tension, Premenstrual", "premenstrual; tension", "Premenstrual Syndrome", "Premenstrual Tensions", "tension; premenstrual", "Tensions, Premenstrual", "Premenstrual tension NOS", "PMT - Premenstrual tension", "Premenstrual tension syndrom", "premenstrual tension syndrome", "Premenstrual tension syndrome", "syndrome; premenstrual tension", "Premenstrual tension syndromes", "premenstrual tension; syndrome", "Premenstrual tension syndrome, NOS", "Premenstrual tension syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "premenstrual tension", "shortest_name_length": 3}
{"curie": "UMLS:C0280345", "names": ["Stage I Mouth Verrucous Carcinoma", "Stage I Oral Cavity Verrucous Cancer", "Stage I Verrucous Carcinoma of Mouth", "Stage I Oral Cavity Verrucous Carcinoma", "Stage I Verrucous Carcinoma of the Mouth", "oral cavity verrucous carcinoma, stage I", "Stage I Verrucous Carcinoma of Oral Cavity", "Stage I Verrucous Carcinoma of the Oral Cavity", "Verrucous carcinoma of the oral cavity stage I", "stage I verrucous carcinoma of the oral cavity", "verrucous carcinoma of the oral cavity, stage I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Verrucous carcinoma of the oral cavity stage I", "shortest_name_length": 33}
{"curie": "MONDO:0037256", "names": ["Serous Neoplasm", "serous neoplasm", "Serous Neoplasms", "Neoplasm, Serous", "Neoplasms, Serous"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "serous neoplasm", "shortest_name_length": 15}
{"curie": "MONDO:0008155", "names": ["Osteomesopycnosis", "osteomesopyknosis", "Osteomesopyknosis", "OSTEOMESOPYKNOSIS", "Axial osteosclerosis", "axial osteosclerosis", "AXIAL OSTEOSCLEROSIS", "Axial osteosclerosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteomesopyknosis", "shortest_name_length": 17}
{"curie": "MONDO:0002058", "names": ["Breast adenoma", "breast adenoma", "Breast Adenoma", "Ademoma - breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast adenoma", "shortest_name_length": 14}
{"curie": "UMLS:C0342490", "names": ["ATROPHY ADRENAL", "adrenal atrophy", "Atrophy adrenal", "Adrenal atrophy", "adrenal; atrophy", "atrophy; adrenal", "Atrophy of adrenal gland", "Adrenal atrophy (disorder)", "adrenal atrophy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adrenal atrophy", "shortest_name_length": 15}
{"curie": "MONDO:0020046", "names": ["autosomal recessive degenerative and progressive cerebellar ataxia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive degenerative and progressive cerebellar ataxia", "shortest_name_length": 66}
{"curie": "UMLS:C1864499", "names": ["Renal Tubular Acidosis, Distal, Autosomal Recessive, with Late-Onset Sensorineural Hearing Loss"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal Tubular Acidosis, Distal, Autosomal Recessive, with Late-Onset Sensorineural Hearing Loss", "shortest_name_length": 95}
{"curie": "UMLS:C2987143", "names": ["PanIN-1B", "Pancreatic Intraepithelial Neoplasia-1B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Intraepithelial Neoplasia-1B", "shortest_name_length": 8}
{"curie": "UMLS:C4744469", "names": ["Cerebral Hemangioblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebral Hemangioblastoma", "shortest_name_length": 25}
{"curie": "MONDO:0035551", "names": ["CARASAL", "cathepsin a-related arteriopathy-strokes-leukoencephalopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cathepsin a-related arteriopathy-strokes-leukoencephalopathy", "shortest_name_length": 7}
{"curie": "UMLS:C5419869", "names": ["Unresectable Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Neuroendocrine Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0002927", "names": ["spindle cell sarcoma", "Spindle cell sarcoma", "Spindle Cell Sarcoma", "sarcoma spindle cell", "spindle cell; sarcoma", "sarcoma; spindle cell", "Spindle Cell Sarcomas", "Sarcoma, Spindle Cell", "Sarcomas, Spindle Cell", "spindle cell sarcoma (diagnosis)", "Undifferentiated Spindle Cell Sarcoma", "Undifferentiated spindle cell sarcoma", "Spindle cell sarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spindle cell sarcoma", "shortest_name_length": 20}
{"curie": "UMLS:C0750906", "names": ["Tactile Amnesia", "Amnesia, Tactile", "Tactile Amnesias", "Amnesias, Tactile"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tactile Amnesia", "shortest_name_length": 15}
{"curie": "MONDO:0008240", "names": ["6PGL DEFICIENCY", "6Pgl deficiency", "6PGL Deficiency", "PGLS DEFICIENCY", "Pgls deficiency", "6-PHOSPHOGLUCONOLACTONASE DEFICIENCY", "6-Phosphogluconolactonase Deficiency", "6-phosphogluconolactonase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "6-phosphogluconolactonase deficiency", "shortest_name_length": 15}
{"curie": "MONDO:0016094", "names": ["vaginal germ cell cancer", "vagina malignant germ cell tumor", "vaginal germ cell malignant tumor", "malignant germ cell tumor of the vagina"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vaginal germ cell malignant tumor", "shortest_name_length": 24}
{"curie": "UMLS:C5205654", "names": ["Refractory Anaplastic Ganglioglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Anaplastic Ganglioglioma", "shortest_name_length": 35}
{"curie": "OMIM:616093", "names": [], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"]}
{"curie": "MONDO:0044302", "names": ["CHDFIDD", "CDK13-Related CHDFIDD", "CDK13-Related Disorder", "congenital heart defects, dysmorphic FACIAL features, and intellectual developmental disorder", "congenital heart defects, dysmorphic facial features, and intellectual developmental disorder", "CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital heart defects, dysmorphic facial features, and intellectual developmental disorder", "shortest_name_length": 7}
{"curie": "UMLS:C0156181", "names": ["Peritoneal band", "peritoneal band", "peritoneal; band", "bands peritoneal", "band; peritoneal", "peritoneal adhesion", "Peritoneal adhesion", "Peritoneal Adhesions", "peritoneum adhesions", "peritoneal adhesions", "adhesion; peritoneum", "Peritoneal adhesions", "peritoneum; adhesion", "PERITONEUM, ADHESIONS", "Peritoneal adhesion, NOS", "Adhesive peritoneal band", "Adhesive peritoneal band, NOS", "Peritoneal adhesion (disorder)", "intra-abdominal adhesions of peritoneum", "intra-abdominal adhesions of peritoneum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peritoneal adhesion", "shortest_name_length": 15}
{"curie": "UMLS:C4552689", "names": ["Stage IA Uterine Corpus Cancer AJCC v8", "Stage IA Uterine (including Endometrial) Cancer", "Stage IA Uterine Corpus Carcinoma or Carcinosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Uterine Corpus Cancer AJCC v8", "shortest_name_length": 38}
{"curie": "UMLS:C4687505", "names": ["Malignant Thymic Germ Cell Tumor Stage Grouping of the Pediatric Study Group", "Malignant Mediastinal Germ Cell Tumor Stage Grouping of the Pediatric Study Group"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Mediastinal Germ Cell Tumor Stage Grouping of the Pediatric Study Group", "shortest_name_length": 76}
{"curie": "MONDO:0021133", "names": ["aFXIII", "FIBRINASE DEFICIENCY, ACQUIRED", "acquired factor XIII deficiency", "Acquired Factor XIII Deficiency", "Acquired factor XIII deficiency", "FACTOR XIII DEFICIENCY, ACQUIRED", "LAKI-LORAND FACTOR DEFICIENCY, ACQUIRED", "FIBRIN STABILIZING FACTOR DEFICIENCY, ACQUIRED", "fibrin-stabilizing factor; deficiency, acquired", "deficiency; fibrin-stabilizing factor, acquired"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired factor XIII deficiency", "shortest_name_length": 6}
{"curie": "UMLS:C0334030", "names": ["Atypical Squamous Metaplasia", "Atypical squamous metaplasia", "Atypical epidermoid metaplasia", "Squamous Metaplasia with Atypia", "Atypical squamous metaplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypical squamous metaplasia", "shortest_name_length": 28}
{"curie": "UMLS:C4726595", "names": ["Refractory Double-Hit Lymphoma", "Refractory High Grade B-Cell Lymphoma with MYC and BCL2 or BCL6 Rearrangements", "Refractory High-Grade B-Cell Lymphoma with MYC and BCL2 or BCL6 Rearrangements"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory High Grade B-Cell Lymphoma with MYC and BCL2 or BCL6 Rearrangements", "shortest_name_length": 30}
{"curie": "UMLS:C1335721", "names": ["Recurrent Urinary Tract Cancer", "Recurrent Urinary Tract Carcinoma", "Recurrent Urinary System Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Urinary System Carcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0010150", "names": ["HNSCC", "SCCHN", "carcinoma of the head and neck", "HEAD NECK CANCER SQUAMOUS CELL", "carcinoma cell head neck squamous", "carcinomas cell head neck squamous", "SQUAMOUS CELL CANCER, HEAD AND NECK", "head and neck squamous cell carcinoma", "Head and Neck Squamous Cell Carcinoma", "Head And Neck Squamous Cell Carcinomas", "Squamous Cell Carcinoma, Head And Neck", "squamous cell carcinoma, head and neck", "SQUAMOUS CELL CARCINOMA, HEAD AND NECK", "Squamous Cell Carcinoma of Head and Neck", "Squamous cell carcinoma of head and neck", "squamous cell carcinoma of head and neck", "squamous cell carcinomas of head and neck", "Carcinoma, Squamous Cell of Head and Neck", "Head and neck squamous cell carcinoma, NOS", "Squamous cell carcinoma of the head and neck", "Squamous Cell Carcinoma of the Head and Neck", "squamous cell carcinoma of the head and neck", "craniocervical region squamous cell carcinoma", "squamous cell carcinoma, head and neck, somatic", "Squamous cell carcinoma of head and neck (disorder)", "[OBSOLETE] Carcinoma, squamous cell of head and neck", "squamous cell carcinoma of head and neck (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "head and neck squamous cell carcinoma", "shortest_name_length": 5}
{"curie": "MONDO:0017473", "names": ["patella aplasia/hypoplasia, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "patella aplasia/hypoplasia, bilateral", "shortest_name_length": 37}
{"curie": "UMLS:C0862468", "names": ["Recurrent Urethral Urothelial Cancer", "Urothelial carcinoma urethra recurrent", "Recurrent Urethral Urothelial Carcinoma", "Recurrent Urothelial Carcinoma of the Urethra"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urothelial carcinoma urethra recurrent", "shortest_name_length": 36}
{"curie": "MONDO:0044792", "names": ["GMN", "LCMN", "CMNS", "GPHN", "spitz nevus", "nevus spilus", "pigmented moles", "PIGMENTED MOLES", "congenital nevus", "giant hairy nevus", "Bathing Trunk Nevus", "Bathing trunk nevus", "bathing trunk nevus", "Bathing trunk naevus", "Giant pigmented mole", "bathing trunk; nevus", "nevus; bathing trunk", "Giant pigmented nevus", "Congenital Skin Nevus", "giant pigmented nevus", "congenital skin nevus", "Giant pigmented naevus", "Giant Congenital Nevus", "congenital hairy nevus", "giant congenital nevus", "congenital nevus of skin", "Congenital Nevus of Skin", "Giant pigmented nevus NOS", "nevus pigmented congenital", "Congenital pigmented nevus", "Giant pigmented naevus NOS", "congenital pigmented nevus", "Giant pigmented nevus, NOS", "GIANT PIGMENTED HAIRY NEVUS", "Giant pigmented naevus, NOS", "congenital pigmented naevus", "giant pigmented hairy nevus", "Congenital pigmented naevus", "Giant pigmented hairy nevus", "Congenital Melanocytic Nevi", "congenital melanocytic nevi", "Congenital Melanocytic Nevus", "Congenital Nevus of the Skin", "congenital nevus of the skin", "Congenital melanocytic nevus", "congenital melanocytic nevus", "Giant Pigmented Nevus of Skin", "Giant pigmented nevus of skin", "congenital melanocytic naevus", "giant pigmented nevus of skin", "Congenital melanocytic naevus", "Giant pigmented naevus of skin", "Congenital Pigmented Skin Nevus", "congenital pigmented skin nevus", "GIANT CONGENITAL PIGMENTED NEVUS", "congenital giant pigmented nevus", "giant congenital pigmented Nevus", "Giant congenital pigmented nevus", "nevus pigmented congenital giant", "Congenital giant pigmented nevus", "giant pigmented nevus of the skin", "Giant Pigmented Nevus of the Skin", "Congenital giant pigmented naevus", "Congenital melanocytic nevus, NOS", "congenital giant naevus pigmented", "Congenital melanocytic naevus, NOS", "Congenital giant melanocytic nevus", "Congenital Pigmented Nevus of Skin", "congenital pigmented nevus of skin", "Giant congenital melanocytic nevus", "large congenital melanocytic nevus", "giant congenital melanocytic nevus", "Congenital pigmented nevus of skin", "Large congenital melanocytic nevus", "Congenital pigmented naevus of skin", "Congenital dermal melanocytic nevus", "Congenital Melanocytic Nevus of Skin", "Congenital melanocytic nevus of skin", "spitz nevus or nevus spilus, somatic", "Congenital dermal melanocytic naevus", "congenital melanocytic nevus of skin", "Congenital melanocytic naevus of skin", "Congenital Pigmented Melanocytic Nevus", "MELANOCYTIC NEVUS SYNDROME, CONGENITAL", "melanocytic nevus syndrome, congenital", "Melanocytic nevus syndrome, congenital", "Congenital Pigmented Nevus of the Skin", "congenital pigmented nevus of the skin", "Congenital pigmented melanocytic nevus", "congenital pigmented melanocytic Nevus", "Congenital pigmented melanocytic naevus", "Intermediate and giant congenital nevus", "Congenital Melanocytic Nevus of the Skin", "congenital melanocytic nevus of the skin", "Congenital giant pigmented nevus of skin", "Intermediate and giant congenital naevus", "Congenital giant pigmented naevus of skin", "Congenital pigmented melanocytic nevus of skin", "Giant pigmented nevus (morphologic abnormality)", "Congenital pigmented melanocytic naevus of skin", "melanocytic nevus syndrome, congenital, somatic", "Congenital pigmented melanocytic nevus (disorder)", "Giant pigmented nevus of uncertain behavior of skin", "Giant pigmented naevus of uncertain behaviour of skin", "Congenital pigmented melanocytic nevus of skin (disorder)", "Giant pigmented nevus of uncertain behavior of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "large congenital melanocytic nevus", "shortest_name_length": 3}
{"curie": "UMLS:C0549445", "names": ["Anemia aggravated", "ANEMIA AGGRAVATED", "ANAEMIA AGGRAVATED", "Anaemia aggravated", "Anemia NOS aggravated", "Anaemia NOS aggravated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anaemia NOS aggravated", "shortest_name_length": 17}
{"curie": "UMLS:C5239042", "names": ["High Risk Chronic Myelogenous Leukemia, BCR-ABL1 Positive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Risk Chronic Myelogenous Leukemia, BCR-ABL1 Positive", "shortest_name_length": 57}
{"curie": "MONDO:0011653", "names": ["NMTC3", "NMTC1, FORMERLY", "thyroid cancer, nonmedullary, 3", "thyroid cancer, nonmedullary, 1", "THYROID CANCER, NONMEDULLARY, 3", "Nonmedullary Thyroid Carcinoma 1", "Thyroid Carcinoma, Nonmedullary 1", "thyroid carcinoma, nonmedullary, 3", "thyroid cancer, nonmedullary, 1, formerly", "THYROID CANCER, NONMEDULLARY, 1, FORMERLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid cancer, nonmedullary, 3", "shortest_name_length": 5}
{"curie": "MONDO:0002375", "names": ["TS", "TSC", "Epiloia", "Epiloya", "Pringle", "epiloia", "EPILOIA", "epiploia", "Bourneville", "phacomatosis", "Pringle tumor", "Pringle tumour", "Brain sclerosis", "brain sclerosis", "Pringle disease", "sclerosis brain", "adenoma sebaceum", "Adenoma sebaceum", "brain; sclerosis", "sclerosis; brain", "Adenoma Sebaceum", "sebaceous adenoma", "Sebaceous adenoma", "Sebaceous Adenoma", "Sebaceous adenomas", "TUBEROSE SCLEROSIS", "Tuberous sclerosis", "Cerebral Scleroses", "tuberose sclerosis", "Tuberose Sclerosis", "tuberous sclerosis", "TUBEROUS SCLEROSIS", "tuberosa sclerosis", "sclerosis tuberous", "cerebral sclerosis", "Sclerosis Tuberosa", "Cerebral Sclerosis", "sclerosis tuberosa", "Tuberous Sclerosis", "Bourneville Disease", "Sclerosis, Tuberose", "tuberous; sclerosis", "sclerosis; tuberous", "Facial angiofibroma", "facial angiofibroma", "Sclerosis, Cerebral", "Bourneville disease", "Sclerosis, Tuberous", "bourneville disease", "angiofibromas facial", "Bourneville syndrome", "Bourneville Syndrome", "Facial angiofibromas", "[M]Sebaceous adenoma", "Bourneville's disease", "sebaceous epithelioma", "Bourneville's Disease", "Syndrome, Bourneville", "Sebaceous epithelioma", "Bourneville's Syndrome", "Sebaceous epitheliomas", "sebaceous gland adenoma", "Sebaceous Gland Adenoma", "Syndrome, Bourneville's", "Adenoma, Sebaceous Cell", "Sebaceous gland adenoma", "TS - Tuberous sclerosis", "neuromatosis universalis", "Bourneville Phakomatosis", "neurinomatosis centralis", "Bourneville Phacomatosis", "Phacomatosis, Bourneville", "Adenoma sebaceum syndrome", "Phakomatosis, Bourneville", "phakomatosis; Bourneville", "Sebaceous adenoma of skin", "PHAKOMATOSIS, BOURNEVILLE", "Bourneville; phakomatosis", "ADENOMA, SEBACEOUS, BENIGN", "Tuberous sclerosis complex", "Adenoma of Sebaceous Gland", "tuberous sclerosis complex", "adenoma, sebaceous, benign", "adenoma of sebaceous gland", "TUBEROUS SCLEROSIS COMPLEX", "Tuberous Sclerosis Complex", "Bourneville Pringle Disease", "Bourneville-Pringle Disease", "tuberous sclerosis syndrome", "Tuberous sclerosis syndrome", "Disease, Bourneville-Pringle", "BOURNEVILLE-PRINGLE SYNDROME", "Bourneville-Brissaud disease", "Bourneville-Pringles Disease", "Bourneville-Pringle syndrome", "Bourneville-Pringle's Disease", "neurospongioblastosis diffusa", "Bourneville Pringle's Disease", "adenoma of the Sebaceous gland", "spongioblastosis circumscripta", "Disease, Bourneville-Pringle's", "tuberous sclerosis (diagnosis)", "adenoma of the sebaceous gland", "Adenoma of the Sebaceous Gland", "skin appendage sebaceous adenoma", "Sebaceous epithelioma (disorder)", "Skin Appendage Sebaceous Adenoma", "Angiokeratoma in tuberous sclerosis", "Sebaceous adenoma of skin (disorder)", "Tuberous sclerosis syndrome (disorder)", "fibrous skin tumor of tuberous sclerosis", "Fibrous skin tumor of tuberous sclerosis", "Fibrous skin tumour of tuberous sclerosis", "hereditary multiple system hamartomatosis", "sebaceous adenoma (morphologic abnormality)", "Sebaceous adenoma (morphologic abnormality)", "Fibrous skin tumor of tuberous sclerosis (disorder)", "fibrous skin tumor of tuberous sclerosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sebaceous adenoma", "shortest_name_length": 2}
{"curie": "MONDO:0030976", "names": ["OCABSN", "oculomotor-abducens synkinesis", "OCULOMOTOR-ABDUCENS SYNKINESIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculomotor-abducens synkinesis", "shortest_name_length": 6}
{"curie": "MONDO:0017997", "names": ["telecanthus-hypertelorism-strabismus-pes cavus syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "telecanthus-hypertelorism-strabismus-pes cavus syndrome", "shortest_name_length": 55}
{"curie": "MONDO:0012699", "names": ["LGMD2M", "MDDGC4", "LGMDR13", "LGMD type 2M", "LGMD-FKTN related", "Fukutin-related LGMD R13", "Autosomal recessive LGMD type 2M", "limb-girdle muscular dystrophy type 2M", "Muscular Dystrophy, Limb-Girdle, Type 2M", "muscular dystrophy, limb-girdle, type 2M", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2M", "Fukutin-related limb-girdle muscular dystrophy R13", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 13", "FKTN autosomal recessive limb-girdle muscular dystrophy", "Autosomal recessive limb girdle muscular dystrophy type 2M", "autosomal recessive limb-girdle muscular dystrophy type 2M", "Autosomal recessive limb-girdle muscular dystrophy type 2M", "muscular dystrophy-dystroglycanopathy (limb-girdle) type C 4", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4", "muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 4", "Autosomal recessive limb girdle muscular dystrophy type 2M (disorder)", "autosomal recessive limb-girdle muscular dystrophy caused by mutation in FKTN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive limb-girdle muscular dystrophy type 2M", "shortest_name_length": 6}
{"curie": "UMLS:C1404574", "names": ["Laryngeal nerve palsy", "Laryngeal Nerve Palsy", "n.laryngeus; paralysis", "Laryngeal Nerve Paralysis", "paralysis; laryngeal nerve"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laryngeal nerve palsy", "shortest_name_length": 21}
{"curie": "MONDO:0001484", "names": ["Paraphrenia - late", "paraphrenia - late", "Paranoid schizophrenia", "SCHIZOPHRENIA PARANOID", "Paranoid Schizophrenia", "schizophrenia paranoid", "paranoid schizophrenia", "Schizophrenia;paranoid", "PARANOID SCHIZOPHRENIA", "Paranoid Schizophrenias", "schizophrenia; paranoid", "Schizophrenia, Paranoid", "paranoid; schizophrenia", "Schizophrenias, Paranoid", "paraphrenic schizophrenia", "Paraphrenic schizophrenia", "schizophrenia; paraphrenic", "paraphrenic; schizophrenic", "SCHIZOPHRENIA PARANOID TYPE", "paranoid schizophrenia type", "PARANOID TYPE SCHIZOPHRENIA", "paranoid type schizophrenia", "Paranoid type schizophrenia", "Paranoid Type Schizophrenia", "Paranoid schizophrenia, NOS", "schizophrenia paranoid type", "Schizophrenia, paranoid type", "Chronic paranoid schizophrenia", "chronic paranoid schizophrenia", "Paranoid schizophrenia (disorder)", "paranoid schizophrenia (diagnosis)", "SCHIZOPHRENIA PARANOID TYPE CHRONIC", "Paranoid type schizophrenia, chronic", "Paranoid type schizophrenia, unspecified", "Chronic paranoid schizophrenia (disorder)", "chronic paranoid schizophrenia (diagnosis)", "Paranoid type schizophrenia, chronic state", "paranoid type schizophrenia subchronic state", "Paranoid type schizophrenia, unspecified state"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paranoid schizophrenia", "shortest_name_length": 18}
{"curie": "UMLS:C4551868", "names": ["Cervical Cancer Stage II", "Stage IIB Cervical Cancer", "AJCC Stage IIB Cervical Cancer", "FIGO Stage IIB Cervix Carcinoma", "Stage IIB Cervical Cancer AJCC v7", "FIGO Stage IIB Cervical Carcinoma", "Stage IIB Cervical Cancer AJCC v6", "FIGO Stage IIB Carcinoma of Cervix", "FIGO Stage IIB Cervix Uteri Carcinoma", "FIGO Stage IIB Carcinoma of the Cervix", "FIGO Stage IIB Uterine Cervix Carcinoma", "Stage IIB Cervical Cancer AJCC v6 and v7", "FIGO Stage IIB Carcinoma of Cervix Uteri", "FIGO Stage IIB Carcinoma of Uterine Cervix", "FIGO Stage IIB Carcinoma of the Cervix Uteri", "FIGO Stage IIB Carcinoma of the Uterine Cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Cervical Cancer AJCC v6 and v7", "shortest_name_length": 24}
{"curie": "MONDO:0017233", "names": ["Familial Alzheimer-like prion disease", "familial Alzheimer-like prion disease", "Familial Alzheimer-like prion disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial Alzheimer-like prion disease", "shortest_name_length": 37}
{"curie": "MONDO:0008573", "names": ["tibial torsion, bilateral medial", "Tibial Torsion, Bilateral Medial", "TIBIAL TORSION, BILATERAL MEDIAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tibial torsion, bilateral medial", "shortest_name_length": 32}
{"curie": "UMLS:C0011268", "names": ["Dementia;senile", "senile dementia", "DEMENTIA SENILE", "Senile dementia", "dementia senile", "Senile Dementia", "senile; dementia", "dementia; senile", "Dementia, Senile", "old age; dementia", "Dementia (Senile)", "dementia; old age", "Senile dementia NOS", "Senile dementia, NOS", "SD - Senile dementia", "Senile dementia (disorder)", "senile dementia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Senile dementia", "shortest_name_length": 15}
{"curie": "UMLS:C1709577", "names": ["Pleural Monophasic Synovial Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pleural Monophasic Synovial Sarcoma", "shortest_name_length": 35}
{"curie": "UMLS:C0581391", "names": ["Chronic depression", "chronic depression", "depression chronic", "chronic depression (symptom)", "Chronic depression (disorder)", "chronic depression (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic depression", "shortest_name_length": 18}
{"curie": "UMLS:C3899640", "names": ["Thyroid Gland Cancer", "Childhood Thyroid Carcinoma", "Childhood Thyroid Gland Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Thyroid Gland Carcinoma", "shortest_name_length": 20}
{"curie": "MONDO:0100452", "names": ["RP87", "retinitis pigmentosa 87", "dominant RPE65 retinopathy", "RPE65-related dominant retinopathy", "retinitis pigmentosa 87 with choroidal involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "RPE65-related dominant retinopathy", "shortest_name_length": 4}
{"curie": "UMLS:C5206443", "names": ["Stage II Cervical Cancer FIGO 2018", "Stage II Cervical Carcinoma FIGO 2018"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Cervical Cancer FIGO 2018", "shortest_name_length": 34}
{"curie": "UMLS:C1336383", "names": ["Stage IVB Mouth Mucoepidermoid Carcinoma", "Stage IVB Oral Cavity Mucoepidermoid Cancer", "Stage IVB Mucoepidermoid Carcinoma of Mouth", "Stage IVB Oral Cavity Mucoepidermoid Carcinoma", "Stage IVB Mucoepidermoid Carcinoma of the Mouth", "Stage IVB Mucoepidermoid Carcinoma of Oral Cavity", "Stage IVB Mucoepidermoid Carcinoma of the Oral Cavity", "Stage IVB Oral Cavity Mucoepidermoid Carcinoma AJCC v7", "Stage IVB Oral Cavity Mucoepidermoid Carcinoma AJCC v6", "Stage IVB Oral Cavity Mucoepidermoid Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Oral Cavity Mucoepidermoid Carcinoma AJCC v6 and v7", "shortest_name_length": 40}
{"curie": "UMLS:C5667307", "names": ["Advanced Appendix Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Appendix Adenocarcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C3714042", "names": ["46,XY Disorder of Sex Development Due To LH Defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XY Disorder of Sex Development Due To LH Defects", "shortest_name_length": 51}
{"curie": "UMLS:C5419800", "names": ["Inflammatory Bowel Disease-Associated Colorectal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Inflammatory Bowel Disease-Associated Colorectal Adenocarcinoma", "shortest_name_length": 63}
{"curie": "MONDO:0009512", "names": ["Lethal Larsen-like syndrome", "lethal Larsen-like syndrome", "LARSEN-LIKE SYNDROME, LETHAL TYPE", "Larsen-Like Syndrome, Lethal Type", "Larsen like syndrome, lethal type", "Larsen-like syndrome, lethal type", "Lethal Larsen-like syndrome (disorder)", "Larsen-like multiple joint dislocation syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal Larsen-like syndrome", "shortest_name_length": 27}
{"curie": "MONDO:0013745", "names": ["JBTS14", "JOUBERT SYNDROME 14", "Joubert syndrome 14", "TMEM237 Joubert syndrome", "Joubert syndrome type 14", "Joubert syndrome caused by mutation in TMEM237"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome 14", "shortest_name_length": 6}
{"curie": "MONDO:0044327", "names": ["PCLD4", "POLYCYSTIC LIVER DISEASE 4 WITH OR WITHOUT KIDNEY CYSTS", "polycystic liver disease 4 with or without kidney cysts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polycystic liver disease 4 with or without kidney cysts", "shortest_name_length": 5}
{"curie": "UMLS:C1720965", "names": ["Ectodermal Dysplasia 3, Anhidrotic", "Ectodermal Dysplasia, Hypohidrotic, Autosomal Dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ectodermal Dysplasia 3, Anhidrotic", "shortest_name_length": 34}
{"curie": "MONDO:0018072", "names": ["TAC", "PTA", "Common truncus", "truncus; common", "common; truncus", "Truncus Arteriosus", "truncus arteriosus", "Truncus arteriosus", "truncus; arteriosus", "arteriosus; truncus", "artery; common trunk", "common arterial trunk", "Common arterial trunk", "common; arterial trunk", "Common truncus arteriosus", "Common Truncus Arteriosus", "common truncus arteriosus", "Truncus Arteriosus Communi", "Common aortopulmonary trunk", "Truncus Arteriosus Communis", "TRUNCUS ARTERIOSUS COMMUNIS", "Truncus arteriosus communis", "CAT - Common arterial trunk", "Arteriosus Communis, Truncus", "Truncus arteriosus persistent", "persistent truncus arteriosus", "common aorticopulmonary trunk", "Common aorticopulmonary trunk", "PERSISTENT TRUNCUS ARTERIOSUS", "Persistent Truncus Arteriosus", "Persistent truncus arteriosus", "Truncus arteriosus, Persistent", "TRUNCUS ARTERIOSUS, PERSISTENT", "Truncus Arteriosus, Persistent", "common arterial trunk (diagnosis)", "Common truncus arteriosus (disorder)", "Common truncus arteriosus (diagnosis)", "persistent truncus arteriosus (disease)", "Common arterial trunk (truncus arteriosus)", "Absent septum between aorta and pulmonary artery", "Persistent truncus arteriosus (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "persistent truncus arteriosus", "shortest_name_length": 3}
{"curie": "MONDO:0006226", "names": ["Gastric MALToma", "gastric MALToma", "MALToma of stomach", "MALToma of Stomach", "stomach MALT lymphoma", "Gastric MALT Lymphoma", "gastric MALT lymphoma", "MALToma of the stomach", "MALToma of the Stomach", "MALT lymphoma of stomach", "MALT Lymphoma of Stomach", "MALT Lymphoma of the Stomach", "MALT lymphoma of the stomach", "Primary Gastric MALT Lymphoma", "primary gastric MALT lymphoma", "Primary MALT Lymphoma of Stomach", "primary MALT lymphoma of stomach", "primary gastric B-cell MALT lymphoma", "Primary MALT Lymphoma of the Stomach", "primary MALT lymphoma of the stomach", "Primary Gastric B-Cell MALT Lymphoma", "MALT lymphoma of stomach (diagnosis)", "gastric mucosa-associated lymphoid tissue lymphoma", "Gastric Mucosa-Associated Lymphoid Tissue Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric mucosa-associated lymphoid tissue lymphoma", "shortest_name_length": 15}
{"curie": "MONDO:0014950", "names": ["AAT10", "AORTIC ANEURYSM, FAMILIAL THORACIC 10", "aortic aneurysm, familial thoracic 10", "aortic aneurysm, familial thoracic type 10", "LOX familial thoracic aortic aneurysm and aortic dissection", "AORTIC ANEURYSM, THORACIC, WITH OR WITHOUT AORTIC DISSECTION", "familial thoracic aortic aneurysm and aortic dissection caused by mutation in LOX"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic aneurysm, familial thoracic 10", "shortest_name_length": 5}
{"curie": "UMLS:C4086288", "names": ["EXTERNAL AURAL FISTULA", "External Auditory Canal Fistula"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "External Auditory Canal Fistula", "shortest_name_length": 22}
{"curie": "UMLS:C0016428", "names": ["eruption cyst", "cyst eruption", "Eruption cyst", "Eruption Cyst", "cyst; eruption", "eruption; cyst", "eruption jaw cyst", "Tooth eruption cyst", "Eruption cyst of jaw", "eruption cyst of jaw", "Follicular cyst of jaw", "Tooth eruption hematoma", "Tooth eruption haematoma", "Eruptive odontogenic cyst", "Cyst, eruptive odontogenic", "Eruption cyst of jaw (disorder)", "eruption cyst of jaw (diagnosis)", "Follicular eruption of cyst of jaw"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eruption cyst of jaw", "shortest_name_length": 13}
{"curie": "MONDO:0011019", "names": ["Devriendt Vandenberghe Fryns syndrome", "Devriendt-Vandenberghe-Fryns syndrome", "alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome", "Alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome", "Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome", "Alopecia-Mental Retardation Syndrome with Convulsions and Hypergonadotropic Hypogonadism", "alopecia-mental retardation syndrome with convulsions and hypergonadotropic hypogonadism", "ALOPECIA-MENTAL RETARDATION SYNDROME WITH CONVULSIONS AND HYPERGONADOTROPIC HYPOGONADISM", "Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder)", "alopecia-intellectual disability syndrome with convulsions and hypergonadotropic hypogonadism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome", "shortest_name_length": 37}
{"curie": "UMLS:C4724831", "names": ["Unresectable Thymic Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Thymic Carcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0002877", "names": ["cervical carcinosarcoma", "Cervical carcinosarcoma", "Cervical Carcinosarcoma", "uterine cervix carcinosarcoma", "Carcinosarcoma of cervix uteri", "Carcinosarcoma of the cervix uteri", "carcinosarcoma of the cervix uteri", "cervical malignant Mullerian mixed tumor", "cervical malignant Müllerian mixed tumor", "cervical malignant mixed Mullerian tumor", "Cervical malignant Müllerian mixed tumor", "Carcinosarcoma of cervix uteri (disorder)", "Malignant Müllerian mixed tumor of cervix uteri", "Malignant Müllerian mixed tumour of cervix uteri", "Malignant Müllerian mixed neoplasm of cervix uteri", "cervical mixed epithelial and mesenchymal neoplasm", "Cervical Mixed Epithelial and Mesenchymal Neoplasm", "malignant Mullerian mixed tumor of the cervix uteri", "cervical malignant mixed mesodermal mullerian tumor", "malignant Müllerian mixed tumor of the cervix uteri", "Malignant Müllerian mixed tumor of the cervix uteri", "Cervical Malignant Mixed Mesodermal (Müllerian) Tumor", "Cervical Malignant Mixed Mesodermal (Mullerian) Tumor", "cervical malignant mixed mesodermal (Mullerian) tumor", "cervical malignant mixed mesodermal (Müllerian) tumor", "Malignant Cervical Mixed Epithelial and Mesenchymal Neoplasm", "Malignant Mixed Epithelial and Mesenchymal Neoplasm of the Cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical carcinosarcoma", "shortest_name_length": 23}
{"curie": "UMLS:C0410719", "names": ["bone deformity", "Bone deformity", "bone; deformity", "deformity; bone", "Bone deformities", "bone deformities", "deformity of bone", "Deformity of bone", "Deformity of bone (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Deformity of bone", "shortest_name_length": 14}
{"curie": "UMLS:C5206636", "names": ["Basaloid PeIN", "Basaloid (Undifferentiated) PeIN", "Basaloid Penile Intraepithelial Neoplasia", "Basaloid (Undifferentiated) Penile Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Basaloid (Undifferentiated) Penile Intraepithelial Neoplasia", "shortest_name_length": 13}
{"curie": "UMLS:C0948693", "names": ["Postoperative discharge", "Post procedural drainage", "Post procedural discharge"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post procedural discharge", "shortest_name_length": 23}
{"curie": "MONDO:0001167", "names": ["Little", "little disease", "Little Disease", "Little disease", "Littles disease", "Little's Disease", "Little's disease", "diplegia spastic", "spastic diplegia", "Spastic Diplegia", "little's disease", "Spastic diplegic", "Spastic diplegia", "Diplegia, Spastic", "Spastic Diplegias", "Spastic diparesis", "Diplegias, Spastic", "Congenital diplegia", "congenital diplegia", "congenital; diplegia", "diplegic cerebral palsy", "Palsy;infantile spastic", "infantile spastic palsy", "Diplegic cerebral palsy", "Spastic diplegia syndrome", "Spastic palsy (infantile)", "spastic infantile paralysis", "infantile spastic paralysis", "Spastic diplegia (disorder)", "Spastic infantile paralysis", "Paralysis;infantile spastic", "PARALYSIS SPASTIC CONGENITAL", "Paralysis spastic congenital", "Congenital spastic paralysis", "Little's disease (diagnosis)", "infantile; paralysis, spastic", "paralysis; congenital, spastic", "congenital; paralysis, spastic", "cerebral palsy spastic diplegia", "cerebral palsy spastic diplegic", "Spastic diplegic cerebral palsy", "Spastic Diplegia Cerebral Palsy", "spastic diplegia cerebral palsy", "Spastic diplegia cerebral palsy", "infantile spastic cerebral palsy", "Infantile spastic cerebral palsy", "Diplegic Infantile Cerebral Palsy", "infantile diplegic cerebral palsy", "Cerebral palsy, spastic, diplegic", "diplegic infantile cerebral palsy", "Diplegic infantile cerebral palsy", "Infantile cerebral palsy, diplegic", "Diplegic cerebral palsy (disorder)", "Infantile Cerebral Palsy, Diplegic", "diplegic cerebral palsy (diagnosis)", "Cerebral Palsy, Diplegic, Infantile", "cerebral spastic infantile paralysis", "Cerebral palsy with spastic diplegia", "spastic; paralysis, cerebral infantile", "paralysis; spastic, cerebral infantile", "paralysis; cerebral, diplegic (spastic)", "cerebral; paralysis, diplegic (spastic)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic diplegia", "shortest_name_length": 6}
{"curie": "MONDO:0003373", "names": ["renal leiomyosarcoma", "Renal Leiomyosarcoma", "Kidney Leiomyosarcoma", "kidney leiomyosarcoma", "Leiomyosarcoma of Kidney", "leiomyosarcoma of kidney", "leiomyosarcoma of the kidney", "Leiomyosarcoma of the Kidney", "leiomyosarcoma of kidney (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kidney leiomyosarcoma", "shortest_name_length": 20}
{"curie": "MONDO:0018907", "names": ["cystoma", "Cystoma", "CRANIOPHARYNGIOMA", "craniopharyngioma", "Craniopharyngioma", "RATHKE POUCH TUMOR", "Rathke Pouch Tumor", "Rathke pouch tumor", "rathke pouch tumor", "craniopharyngiomas", "Craniopharyngiomas", "Tumor, Rathke Pouch", "Rathkes Pouch Tumor", "Rathke's Pouch Tumor", "Rathke's pouch tumor", "[M]Craniopharyngioma", "Rathke pouch neoplasm", "Rathke Cleft Neoplasm", "Rathke's pouch tumour", "rathke's pouch tumour", "tumor; Rathke's pouch", "Rathke Pouch Neoplasm", "Rathke's pouch; tumor", "Tumor, Rathke's Pouch", "Neoplasm, Rathke Cleft", "Rathkes Cleft Neoplasm", "Adamantinomatous tumor", "[M]Rathke's pouch tumor", "Tumor of Rathke's Pouch", "tumor of Rathke's pouch", "Neoplasm, Rathkes Cleft", "ADAMANTINOMA, PITUITARY", "Rathke's Cleft Neoplasm", "Rathke's Pouch Neoplasm", "Rathke's pouch neoplasm", "[M]Rathke's pouch tumour", "Neoplasm, Rathke's Cleft", "CRANIOPHARYNGIOMA, BENIGN", "craniopharyngioma, benign", "Neoplasm of Rathke's Pouch", "neoplasm of Rathke's Pouch", "neoplasm of Rathke's pouch", "PITUITARY EPIDERMOID TUMOR", "craniopharyngeal duct tumor", "Craniopharyngioma (disorder)", "craniopharyngioma (diagnosis)", "BRAIN TUMOR, CRANIOPHARYNGIOMA", "craniopharyngioma (WHO grade I)", "Dysodontogenic epithelial tumor", "Craniopharyngioma (WHO Grade 1)", "Craniopharyngioma (WHO Grade I)", "INTRACRANIAL NEOPLASM, CRANIOPHARYNGIOMA", "craniopharyngioma (morphologic abnormality)", "Craniopharyngioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniopharyngioma", "shortest_name_length": 7}
{"curie": "MONDO:0007062", "names": ["adactylia unilateral", "Adactylia, Unilateral", "adactylia, unilateral", "ADACTYLIA, UNILATERAL", "Adactyly of hand, unilateral", "Digits 2-5 hypodactyly, unilateral", "digits 2-5 hypodactyly, unilateral", "Digits 2-5 oligodactyly, unilateral", "digits 2-5 oligodactyly, unilateral", "TERMINAL TRANSVERSE DEFECTS OF HAND, UNILATERAL", "Terminal Transverse Defects of Hand, Unilateral", "terminal transverse defects of hand, unilateral", "congenital absence/hypoplasia of fingers excluding thumb, unilateral", "Congenital absence/hypoplasia of fingers excluding thumb, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital absence/hypoplasia of fingers excluding thumb, unilateral", "shortest_name_length": 20}
{"curie": "UMLS:C5556766", "names": ["Refractory Clear Cell Sarcoma of Soft Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Clear Cell Sarcoma of Soft Tissue", "shortest_name_length": 44}
{"curie": "EFO:0010133", "names": ["diabetic maculopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diabetic maculopathy", "shortest_name_length": 20}
{"curie": "MONDO:0013904", "names": ["MDDGA8", "muscle-eye-brain-POMGNT2 related", "POMGNT2 muscular dystrophy-dystroglycanopathy, type A", "congenital muscular dystrophy-dystroglycanopathy type A8", "Walker-Warburg syndrome or muscle-eye-brain disease GTDC2-related", "WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, GTDC2-RELATED", "Walker-Warburg syndrome or muscle-eye-brain disease, Gtdc2-related", "muscular dystrophy-dystroglycanopathy, type A caused by mutation in POMGNT2", "congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A8", "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 8", "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 8", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 8", "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 8", "shortest_name_length": 6}
{"curie": "MONDO:0003173", "names": ["brainstem astrocytoma", "Brainstem Astrocytoma", "Brainstem astrocytoma", "Brain Stem Astrocytoma", "brain stem astrocytoma", "Astrocytoma of brain stem", "brain stem astrocytic neoplasm", "Astrocytoma of brain stem (disorder)", "Astrocytoma of brain stem (diagnosis)", "brain tumor malignant astrocytoma stem", "brainstem astrocytoma (excluding glioblastoma)", "astrocytoma (excluding glioblastoma) of brainstem"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brain stem astrocytic neoplasm", "shortest_name_length": 21}
{"curie": "UMLS:C0152965", "names": ["STAPH SEPSIS", "staph sepsis", "sepsis staph", "staphylococcemia", "bacteremia staph", "staph bacteremia", "STAPH BACTEREMIA", "Staphylococcal sepsis", "staphylococcal sepsis", "staphylococcus; sepsis", "sepsis; Staphylococcus", "Staphylococcal bacteremia", "staphylococcal bacteremia", "SEPTICEMIA STAPHYLOCOCCAL", "Septicemia staphylococcal", "staphylococcal septicemia", "Staphylococcal septicemia", "Staphylococcal septicaemia", "Septicaemia staphylococcal", "staphylococcal septicaemia", "Staphylococcal bacteraemia", "SEPTICAEMIA STAPHYLOCOCCAL", "staphylococcal septicemia (diagnosis)", "staphylococcal bacteremia (diagnosis)", "Staphylococcal septicemia, unspecified", "Septicemia due to unspecified staphylococcus", "Septicaemia due to unspecified staphylococcus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Staphylococcal bacteremia", "shortest_name_length": 12}
{"curie": "MONDO:0016141", "names": ["alpha-sarcoglycanopathy", "qualitative or quantitative defects of alpha-sarcoglycan"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of alpha-sarcoglycan", "shortest_name_length": 23}
{"curie": "UMLS:C0042300", "names": ["valvular incompetence", "Valvular incompetence", "valvular insufficiency", "Valvular insufficiency", "valvular regurgitation", "Valvular regurgitation", "regurgitation valvular", "valvular incompetence NOS", "valvular insufficiency NOS", "valvular regurgitation NOS", "Incompetence of any valvular structure", "Valvular insufficiency (morphologic abnormality)", "Incompetence of any valvular structure (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Valvular regurgitation", "shortest_name_length": 21}
{"curie": "MONDO:0001682", "names": ["Diphtheritic peritonitis", "diphtheritic peritonitis", "Diphtheritic peritonitis (disorder)", "diphtheritic peritonitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diphtheritic peritonitis", "shortest_name_length": 24}
{"curie": "UMLS:C1318559", "names": ["Fusospirochetal pharyngitis", "pharyngitis fusospirochetal", "PHARYNGITIS, FUSOSPIROCHETAL", "fusospirochetal; pharyngitis", "Fusospirochaetal pharyngitis", "pharyngitis; fusospirochetal", "Fusospirochetal pharyngitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fusospirochetal pharyngitis", "shortest_name_length": 27}
{"curie": "UMLS:C0275556", "names": ["sinusitis acute bacterial", "Acute bacterial sinusitis", "Acute bacterial sinusitis (disorder)", "Acute bacterial sinusitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute bacterial sinusitis", "shortest_name_length": 25}
{"curie": "MONDO:0001308", "names": ["DEPOSIT CORNEAL", "Corneal deposit", "CORNEAL DEPOSIT", "Deposit corneal", "cornea; deposit", "corneal deposit", "corneal deposits", "Corneal deposits", "CORNEAL DEPOSITS", "deposits - cornea", "Deposits - cornea", "Corneal deposit, NOS", "Corneal deposit (disorder)", "Unspecified corneal deposit", "corneal deposits (diagnosis)", "unspecified corneal deposits", "Corneal deposit, unspecified", "unspecified corneal deposits (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal deposit", "shortest_name_length": 15}
{"curie": "MONDO:0009144", "names": ["EBSTEIN ANOMALY", "Ebstein Anomaly", "Ebstein anomaly", "ebstein anomaly", "ebsteins anomaly", "Ebsteins anomaly", "anomaly; Ebstein", "Anomaly, Ebstein", "Ebsteins Anomaly", "Ebstein; anomaly", "Ebstein's anomaly", "ebstein's anomaly", "syndrome; Ebstein", "Ebstein's Anomaly", "Anomaly, Ebstein's", "anomalies ebstein's", "Ebstein malformation", "Ebstein Malformation", "Ebsteins Malformation", "Ebstein's Malformation", "Ebstein's malformation", "Malformation, Ebstein's", "Ebstein anomaly (disease)", "Ebstein; anomaly or syndrome", "Ebstein's anomaly (diagnosis)", "anomaly ebstein tricuspid valve", "TRICUSPID VALVE, EBSTEIN ANOMALY", "Ebstein anomaly of tricuspid valve", "tricuspid (valve); anomaly, Ebstein", "anomaly; tricuspid (valve), Ebstein", "Ebstein's Anomaly of Tricuspid Valve", "Ebstein's anomaly of tricuspid valve", "Ebstein anomaly of the tricuspid valve", "Ebstein's malformation, tricuspid valve", "Ebstein's anomaly of the tricuspid valve", "Ebstein's anomaly (disorder) [ambiguous]", "Ebstein's malformation of tricuspid valve", "Ebstein malformation of the tricuspid valve", "Ebstein's anomaly of tricuspid valve (disorder)", "tricuspid (valve); deformity, congenital, Ebstein", "Ebstein's anomaly of right atrioventricular valve", "deformity; tricuspid (valve), congenital, Ebstein", "Ebstein's anomaly of common atrioventricular valve"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ebstein anomaly", "shortest_name_length": 15}
{"curie": "UMLS:C0011609", "names": ["Drug Rash", "drug rash", "Drug rash", "DRUG RASH", "drug; rash", "drugs rash", "rash; drug", "Drug eruption", "Drug Eruption", "drug eruption", "DRUG ERUPTION", "DRUG ERUPTIONS", "drug; eruption", "Drug rash, NOS", "Eruption, Drug", "Drug Skin Rash", "drug eruptions", "eruption; drug", "Drug Eruptions", "Eruptions, Drug", "Drug-induced rash", "drug induced rash", "Drug-Induced Rash", "Drug eruption NOS", "Drug eruption, NOS", "Eruption due to drug", "drug induced dermatits", "Dermatitis;drug induced", "DERMATITIS DRUG INDUCED", "drug induced dermatitis", "Drug-induced dermatosis", "Eruption caused by drug", "drug-induced dermatosis", "Dermatitis medicamentosa", "Dermatitis Medicamentosa", "medicamentosa dermatitis", "DERMATITIS MEDICAMENTOSA", "dermatitis medicamentosa", "Eruption due to drug, NOS", "DERMATITIS, MEDICAMENTOSA", "Dermatitis medicamentosa NOS", "Drug-induced cutaneous eruption", "Dermatitis, Adverse Drug Reaction", "Drug-induced dermatosis (disorder)", "Eruption caused by drug (disorder)", "drug-induced dermatosis (diagnosis)", "dermatitis medicamentosa (diagnosis)", "generalized dermatitis due to drugs and medicines", "generalized dermatitis due to drugs and medicines (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drug Eruptions", "shortest_name_length": 9}
{"curie": "MONDO:0015405", "names": ["CAMS", "cerebrofacial arteriovenous metameric syndrome", "Cerebrofacial arteriovenous metameric syndrome", "Cerebrofacial arteriovenous metameric syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebrofacial arteriovenous metameric syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0013320", "names": ["Del(16)(p11.2p12.2)", "monosomy 16p11.2p12.2", "Monosomy 16p11.2p12.2", "monosomy 16p11.2-p12.2", "16p11.2p12.2 microdeletion syndrome", "16p11.2-p12.2 microdeletion syndrome", "chromosome 16p12.2-p11.2 deletion syndrome", "16p11.2p12.2 microdeletion syndrome (disorder)", "chromosome 16p12.2-p11.2 deletion syndrome, isolated cases", "chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-MB", "CHROMOSOME 16p12.2-p11.2 DELETION SYNDROME, 7.1- TO 8.7-MB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 16p12.2-p11.2 deletion syndrome", "shortest_name_length": 19}
{"curie": "UMLS:C2205189", "names": ["Anal NEC", "Anal NEC G3", "Anal Canal NEC", "Anal Canal NEC G3", "Anal Neuroendocrine Carcinoma", "Anal Canal Neuroendocrine Carcinoma", "neuroendocrine carcinoma of anal canal", "Anal High Grade Neuroendocrine Carcinoma", "Anal Canal High Grade Neuroendocrine Carcinoma", "neuroendocrine carcinoma of anal canal (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuroendocrine carcinoma of anal canal", "shortest_name_length": 8}
{"curie": "MONDO:0011334", "names": ["LMS", "LIMB-MAMMARY SYNDROME", "Limb-mammary syndrome", "Limb mammary syndrome", "limb-mammary syndrome", "Limb mammary syndrome (disorder)", "mammary hypoplasia, ectrodactyly, and other hand/foot anomalies", "Mammary hypoplasia, ectrodactyly, and other hand-foot anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "limb-mammary syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0015648", "names": ["startle epilepsy", "Startle epilepsy", "epilepsy reflex startle", "Startle epilepsy (disorder)", "Startle epilepsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "startle epilepsy", "shortest_name_length": 16}
{"curie": "UMLS:C0271148", "names": ["Secondary open-angle glaucoma", "Secondary Open Angle Glaucoma", "secondary open-angle glaucoma", "Glaucoma, Secondary Open Angle", "Glaucoma, open angle, secondary", "Secondary open-angle glaucoma, NOS", "Secondary open-angle glaucoma (disorder)", "secondary open-angle glaucoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary Open Angle Glaucoma", "shortest_name_length": 29}
{"curie": "MONDO:0020320", "names": ["AM", "M2", "FAB M2", "AML M2", "LAM M2", "AML with maturation", "AML with Maturation", "M2 Acute Myeloid Leukemia", "M2 acute myeloid leukemia", "Acute M2 Myeloid Leukemia", "acute M2 myeloid leukemia", "Myeloid Leukemia, Acute, M2", "Leukemia, Myeloid, Acute, M2", "M2 Acute Myelogenous Leukemia", "M2 acute myelogenous leukemia", "acute myeloblastic leukemia M2", "M2 acute granulocytic leukemia", "M2 Acute Myeloblastic Leukemia", "Acute myeloblastic leukemia M2", "M2 Acute Granulocytic Leukemia", "M2 acute myeloblastic leukemia", "Acute Myeloid Leukemia (AML-M2)", "acute myeloid leukemia (AML-M2)", "acute myeloblastic leukemia type 2", "acute myeloid leukemia with maturation", "Acute myeloid leukemia with maturation", "Acute Myeloid Leukemia with Maturation", "Acute myeloid leukaemia with maturation", "Acute myelocytic leukemia with maturation", "M2 acute myeloid leukemia with maturation", "Acute Myelocytic Leukemia with Maturation", "acute myelocytic leukemia with maturation", "M2 Acute Myeloid Leukemia with Maturation", "acute myelogenous leukemia with maturation", "Acute myelogenous leukemia with maturation", "Acute Myelogenous Leukemia with Maturation", "Acute myelocytic leukaemia with maturation", "Acute myelogenous leukaemia with maturation", "Acute granulocytic leukemia with maturation", "Acute myeloblastic leukemia with maturation", "Acute Myeloblastic Leukemia with Maturation", "acute myeloblastic leukemia with maturation", "M2 Acute Myelocytic Leukemia with Maturation", "Acute myeloblastic leukaemia with maturation", "Acute granulocytic leukaemia with maturation", "M2 acute myelocytic leukemia with maturation", "Acute myeloblastic leukemia (with maturation)", "M2 Acute Myelogenous Leukemia with Maturation", "M2 acute myelogenous leukemia with maturation", "M2 Acute Myeloblastic Leukemia with Maturation", "M2 acute myeloblastic leukemia with maturation", "Acute myeloid leukemia with maturation, FAB M2", "Acute myeloid leukaemia with maturation, FAB M2", "acute myelogenous leukemia (AML) with maturation", "M2 - Acute myeloblastic leukemia with maturation", "M2 - Acute myeloblastic leukaemia with maturation", "acute myelogenous leukemia with maturation (diagnosis)", "Acute myeloid leukemia with maturation, FAB M2 (disorder)", "Acute myeloid leukemia with maturation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloblastic leukemia with maturation", "shortest_name_length": 2}
{"curie": "UMLS:C0000822", "names": ["Tubal Abortion", "Tubal abortion", "Abortion, Tubal", "Tubal Abortions", "tubal; abortion", "abortion; tubal", "Abortions, Tubal", "Miscarriage of tubal ectopic pregnancy", "Miscarriage of tubal ectopic pregnancy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abortion, Tubal", "shortest_name_length": 14}
{"curie": "MONDO:0016053", "names": ["isolated cerebellar vermis hypoplasia", "Isolated cerebellar vermis hypoplasia", "Isolated hypoplasia of cerebellar vermis", "Isolated hypoplasia of cerebellar vermis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated cerebellar vermis hypoplasia", "shortest_name_length": 37}
{"curie": "MONDO:0018053", "names": ["TTD", "Trichothiodystrophy", "trichothiodystrophy", "Trichothiodystrophies", "trichothiodystrophy syndrome", "Trichothiodystrophy Syndrome", "Trichothiodystrophy Syndromes", "Trichothiodystrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichothiodystrophy", "shortest_name_length": 3}
{"curie": "UMLS:C0263664", "names": ["Generalized Morphea", "Generalized morphea", "morphea generalized", "generalized morphea", "Generalised morphoea", "Morphea, generalized", "Generalized morphoea", "Generalized scleroderma", "Generalised scleroderma", "Generalized morphea (disorder)", "generalized morphea (diagnosis)", "Circumscribed scleroderma, generalized type", "Circumscribed scleroderma, generalised type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Generalized morphea", "shortest_name_length": 19}
{"curie": "MONDO:0010812", "names": ["MACROCYTOSIS, FAMILIAL", "macrocytosis, familial", "Macrocytosis, Familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macrocytosis, familial", "shortest_name_length": 22}
{"curie": "MONDO:0013781", "names": ["FHHT", "PHA2D", "Pseudohypoaldosteronism type 2D", "pseudohypoaldosteronism type 2D", "pseudohypoaldosteronism, type 2D", "PSEUDOHYPOALDOSTERONISM, TYPE IID", "pseudohypoaldosteronism, type IID", "FAMILIAL HYPERKALEMIC HYPERTENSION", "familial hyperkalemic hypertension", "KLHL3 pseudohypoaldosteronism type 2", "pseudohypoaldosteronism type 2 caused by mutation in KLHL3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudohypoaldosteronism type 2D", "shortest_name_length": 4}
{"curie": "MONDO:0011494", "names": ["HYALURONAN METABOLISM, DEFECT IN", "hyaluronan metabolism, defect IN", "hyaluronan metabolism, defect 1N", "Hyaluronan Metabolism, Defect in", "hyaluronan metabolism, defect type 1N"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyaluronan metabolism, defect 1N", "shortest_name_length": 32}
{"curie": "UMLS:C3899672", "names": ["childhood CNS embryonal tumor", "Central Nervous System Embryonal Neoplasm", "Childhood Central Nervous System Embryonal Tumor", "childhood central nervous system embryonal tumor", "Childhood Central Nervous System Embryonal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Central Nervous System Embryonal Neoplasm", "shortest_name_length": 29}
{"curie": "MONDO:0019453", "names": ["RCMD", "MDS-MLD", "Refractory cytopenia with multilineage dysplasia", "refractory cytopenia with multilineage dysplasia", "Refractory Cytopenia with Multilineage Dysplasia", "Refractory cytopaenia with multilineage dysplasia", "myelodysplastic syndrome with multilineage dysplasia", "Myelodysplastic syndrome with multilineage dysplasia", "Myelodysplastic Syndrome with Multilineage Dysplasia", "refractory cytopenia with multilineage dysplasia (diagnosis)", "Myelodysplastic syndrome with multilineage dysplasia (disorder)", "Myelodysplastic syndrome with multilineage dysplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myelodysplastic syndrome with multilineage dysplasia", "shortest_name_length": 4}
{"curie": "MONDO:0019878", "names": ["dup(3)(q26)", "trisomy 3q26", "dup(3q) syndrome", "3q26 microduplication syndrome", "Cornelia de Lange-like syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "3q26 microduplication syndrome", "shortest_name_length": 11}
{"curie": "UMLS:C5418904", "names": ["Advanced Adenocarcinoma of Unknown Primary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Adenocarcinoma of Unknown Primary", "shortest_name_length": 42}
{"curie": "UMLS:C1334423", "names": ["Grade I Glandular Intraepithelial Neoplasia", "Grade 1 Glandular Intraepithelial Neoplasia", "Glandular intraepithelial neoplasia, grade I", "Low Grade Glandular Intraepithelial Neoplasia", "Glandular intraepithelial neoplasia, low grade", "Glandular intraepithelial neoplasia, low grade (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Glandular intraepithelial neoplasia, low grade", "shortest_name_length": 43}
{"curie": "UMLS:C3665763", "names": ["Instillation site swelling"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Instillation site swelling", "shortest_name_length": 26}
{"curie": "MONDO:0018085", "names": ["umbilical ulceration and intestinal atresia", "Umbilical ulceration and intestinal atresia", "umbilical cord ulcer with intestinal atresia", "Umbilical cord ulcer with intestinal atresia", "umbilical cord ulceration and intestinal atresia", "Umbilical cord ulceration and intestinal atresia", "umbilical cord ulceration-intestinal atresia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "umbilical cord ulceration-intestinal atresia syndrome", "shortest_name_length": 43}
{"curie": "MONDO:0003340", "names": ["Glomoid sarcoma", "sarcoma; glomoid", "glomoid; sarcoma", "glomangiosarcoma", "Glomangiosarcoma", "malignant glomus tumor", "Malignant Glomus Tumor", "Glomus tumor, malignant", "glomus tumor, malignant", "Glomus tumour, malignant", "malignant glomus neoplasm", "Malignant Glomus Neoplasm", "malignant Glomus neoplasm", "glomangiosarcoma (diagnosis)", "Glomangiosarcoma (morphologic abnormality)", "Glomus tumor, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant glomus tumor", "shortest_name_length": 15}
{"curie": "MONDO:0024363", "names": ["rapid eye movement sleep disorder", "Repeated rapid eye movement sleep interruptions", "repeated rapid eye movement sleep interruptions", "Repeated rapid eye movement sleep interruptions (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rapid eye movement sleep disorder", "shortest_name_length": 33}
{"curie": "UMLS:C5555620", "names": ["Ovarian Dedifferentiated Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Dedifferentiated Carcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0015005", "names": ["EPVB6D", "early-onset vitamin B6-dependent epilepsy", "EPILEPSY, EARLY-ONSET, VITAMIN B6-DEPENDENT", "epilepsy, early-onset, vitamin B6-dependent", "epilepsy, early-onset, vitamin B6-dependent; EPVB6D"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, early-onset, vitamin B6-dependent", "shortest_name_length": 6}
{"curie": "MONDO:0015933", "names": ["isolated urogenital tract malformation of male", "nonsyndromic urogenital tract malformation of male", "non-syndromic urogenital tract malformation of male", "male organism non-syndromic urogenital tract malformation", "non-syndromic urogenital tract malformation of male organism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-syndromic urogenital tract malformation of male", "shortest_name_length": 46}
{"curie": "MONDO:0014071", "names": ["MDDGA11", "B3GALNT2 muscular dystrophy-dystroglycanopathy, type A", "congenital muscular dystrophy-dystroglycanopathy type A11", "Walker-Warburg syndrome or muscle-eye-brain disease B3GALNT2-related", "WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, B3GALNT2-RELATED", "Walker-Warburg syndrome or muscle-eye-brain disease, B3Galnt2-related", "muscular dystrophy-dystroglycanopathy, type A caused by mutation in B3GALNT2", "congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A11", "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 11", "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 11", "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11", "shortest_name_length": 7}
{"curie": "MONDO:0002597", "names": ["notochord tumor", "notochord cancer", "notochordal tumor", "Notochordal Tumor", "notochordal cancer", "tumor of notochord", "notochord neoplasm", "cancer of notochord", "notochordal neoplasm", "Notochordal Neoplasm", "neoplasm of notochord", "malignant notochord neoplasm", "malignant neoplasm of notochord"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "notochordal tumor", "shortest_name_length": 15}
{"curie": "MONDO:0003214", "names": ["apocrine carcinoma", "Apocrine Carcinoma", "apocrine adenocarcinoma", "Apocrine adenocarcinoma", "Apocrine gland carcinoma", "Apocrine Gland Carcinoma", "apocrine gland carcinoma", "Carcinoma of Apocrine Gland", "Carcinoma of apocrine gland", "carcinoma of apocrine gland", "apocrine gland adenocarcinoma", "carcinoma of the Apocrine gland", "carcinoma of the apocrine gland", "apocrine adenocarcinoma (diagnosis)", "Carcinoma of apocrine gland (disorder)", "adenocarcinoma; apocrine, unspecified site", "apocrine; adenocarcinoma, unspecified site", "Apocrine adenocarcinoma (morphologic abnormality)", "apocrine adenocarcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "apocrine adenocarcinoma", "shortest_name_length": 18}
{"curie": "UMLS:C2609042", "names": ["Post embolization syndrome", "Post embolisation syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post embolization syndrome", "shortest_name_length": 26}
{"curie": "UMLS:C4330858", "names": ["OED", "Oral dysplasia", "Oral Dysplasia", "Oral Epithelial Dysplasia", "Oral epithelial dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral Epithelial Dysplasia", "shortest_name_length": 3}
{"curie": "MONDO:0011279", "names": ["DFNB17", "autosomal recessive deafness 17", "Deafness, Autosomal Recessive 17", "deafness, autosomal recessive 17", "DEAFNESS, AUTOSOMAL RECESSIVE 17", "autosomal recessive nonsyndromic deafness 17", "autosomal recessive nonsyndromic hearing loss 17", "autosomal recessive nonsyndromic deafness type 17"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 17", "shortest_name_length": 6}
{"curie": "MONDO:0003979", "names": ["Intrahepatic Bile Duct MCN", "intrahepatic bile duct cystadenoma", "Intrahepatic Bile Duct Cystadenoma", "cystadenoma of intrahepatic bile duct", "cystadenoma of the intrahepatic bile duct", "Cystadenoma of the Intrahepatic bile duct", "intrahepatic bile duct mucinous cystic neoplasm", "Intrahepatic Bile Duct Mucinous Cystic Neoplasm", "cystadenoma of intrahepatic bile duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intrahepatic bile duct cystadenoma", "shortest_name_length": 26}
{"curie": "MONDO:0019769", "names": ["X-linked intellectual disability, Sutherland-Haan type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability, Sutherland-Haan type", "shortest_name_length": 54}
{"curie": "UMLS:C0549202", "names": ["chapped skin", "SKIN CHAPPED", "Skin chapped", "Chapped skin", "chapping skin", "Chapping of skin", "Desiccation eczema", "Chapped skin (finding)", "Desiccation eczema (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chapped skin", "shortest_name_length": 12}
{"curie": "MONDO:0013161", "names": ["LGMD2O", "MDDGC3", "LGMDR15", "LGMD type 2O", "LGMD-POMGNT1 related", "POMGNT1-related LGMD R15", "limb-girdle muscular dystrophy type 2O", "Limb-girdle muscular dystrophy type 2O", "muscular dystrophy, limb-girdle, type 2O", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2O", "POMGNT1-related limb-girdle muscular dystrophy R15", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 15", "Limb-girdle muscular dystrophy 2O POMGNT1 gene mutation", "autosomal recessive limb-girdle muscular dystrophy type 2O", "POMGNT1 autosomal recessive limb-girdle muscular dystrophy", "Autosomal recessive limb girdle muscular dystrophy type 2O", "Autosomal recessive limb-girdle muscular dystrophy type 2O", "muscular dystrophy-dystroglycanopathy (limb-girdle) type C3", "muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 3", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3", "muscular dystrophy-dystroglycanopathy limb-girdle POMGNT1-related", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, POMGNT1-RELATED", "muscular dystrophy-dystroglycanopathy, limb-girdle, POMGNT1-related", "Autosomal recessive limb girdle muscular dystrophy type 2O (disorder)", "autosomal recessive limb-girdle muscular dystrophy caused by mutation in POMGNT1", "Limb-girdle muscular dystrophy 2O POMGNT1 (protein o-mannose beta-1,2-n-acetylglucosaminyltransferase) gene mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive limb-girdle muscular dystrophy type 2O", "shortest_name_length": 6}
{"curie": "MONDO:0024247", "names": ["Benign Eccrine Tumor", "benign eccrine tumor", "Benign Eccrine Neoplasm", "benign eccrine neoplasm", "Benign Eccrine Skin Tumor", "benign eccrine skin tumor", "benign eccrine skin neoplasm", "Benign Eccrine Tumor of Skin", "benign eccrine tumor of skin", "Benign Eccrine Skin Neoplasm", "Benign Eccrine Neoplasm of Skin", "benign eccrine neoplasm of skin", "Benign Eccrine Tumor of the Skin", "benign eccrine tumor of the skin", "benign eccrine sweat gland neoplasm", "Benign Eccrine Neoplasm of the Skin", "benign eccrine neoplasm of the skin", "eccrine sweat gland neoplasm, benign", "benign skin tumor with eccrine differentiation", "Benign skin tumor with eccrine differentiation", "Benign skin tumour with eccrine differentiation", "Benign skin tumor with eccrine differentiation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign eccrine neoplasm", "shortest_name_length": 20}
{"curie": "MONDO:0022577", "names": ["billet-bear syndrome", "Billet bear syndrome", "Lower limb partial duplication renal agenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Billet bear syndrome", "shortest_name_length": 20}
{"curie": "UMLS:C4055108", "names": ["Pelvic Elimination Syndrome", "Dysfunctional Elimination Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dysfunctional Elimination Syndrome", "shortest_name_length": 27}
{"curie": "UMLS:C0334629", "names": ["Grade 1 Nodular Sclerosis Hodgkin Lymphoma", "Grade I Nodular Sclerosis Hodgkin's Lymphoma", "Hodgkin lymphoma, nodular sclerosis, grade 1", "Grade 1 Nodular Sclerosis Hodgkin's Lymphoma", "Hodgkin; nodular sclerosis, mixed cellularity", "Hodgkin; mixed cellularity, nodular sclerosis", "Grade 1 Nodular Sclerosis Classic Hodgkin Lymphoma", "Grade 1 Nodular Sclerosis Classical Hodgkin Lymphoma", "Hodgkin; lymphocytic predominance, nodular sclerosis", "Hodgkin; nodular sclerosis, lymphocytic predominance", "Hodgkin disease, nodular sclerosis, mixed cellularity", "Hodgkin disease, nodular sclerosis - mixed cellularity", "Classical Hodgkin lymphoma, nodular sclerosis, grade 1", "Hodgkin's Disease, Nodular Sclerosis, Mixed Cellularity", "Hodgkin's disease, nodular sclerosis, mixed cellularity", "Hodgkin's disease, nodular sclerosis - mixed cellularity", "disease; Hodgkin's, nodular sclerosis, mixed cellularity", "disease; Hodgkin's, mixed cellularity, nodular sclerosis", "nodular sclerosis Hodgkin lymphoma with mixed cellularity", "Hodgkin lymphoma, nodular sclerosis with mixed cellularity", "Hodgkin disease, nodular sclerosis, lymphocyte predominance", "Hodgkin's Disease, Nodular Sclerosis, Lymphocyte Predominance", "Hodgkin disease, nodular sclerosis - lymphocytic predominance", "Hodgkin's disease, nodular sclerosis, lymphocytic predominance", "disease; Hodgkin's, nodular sclerosis, lymphocytic predominance", "Hodgkin's disease, nodular sclerosis - lymphocytic predominance", "nodular sclerosis Hodgkin lymphoma with lymphocytic predominance", "Hodgkin lymphoma nodular sclerosis with lymphocytic predominance", "Hodgkin's disease, nodular sclerosis - mixed cellularity (disorder)", "nodular sclerosis Hodgkin lymphoma with mixed cellularity (diagnosis)", "Hodgkin lymphoma, nodular sclerosis, grade 1 (morphologic abnormality)", "Hodgkin's disease, nodular sclerosis - lymphocytic predominance (disorder)", "nodular sclerosis Hodgkin lymphoma with lymphocytic predominance (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's disease, nodular sclerosis - mixed cellularity", "shortest_name_length": 42}
{"curie": "MONDO:0001769", "names": ["Acquired dacryostenosis", "acquired tear duct stenosis", "Acquired tear duct stenosis", "tear duct - acquired stenosis", "Tear duct - acquired stenosis", "acquired nasolacrimal duct stenosis", "Acquired nasolacrimal duct stenosis", "Acquired stenosis of nasolacrimal duct", "acquired stenosis of nasolacrimal duct", "stenosis of nasolacrimal duct, acquired", "Stenosis of nasolacrimal duct, acquired", "lacrimal stenosis nasolacrimal duct acquired", "Acquired nasolacrimal duct stenosis (disorder)", "acquired stenosis of nasolacrimal duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired tear duct stenosis", "shortest_name_length": 23}
{"curie": "MONDO:0017575", "names": ["MNGIE", "mngie", "OGIMD", "POLIP", "MNGIE Disease", "MNGIE Syndrome", "MNGIE syndrome", "MNGIE syndrome (diagnosis)", "thymidine phosphorylase deficiency", "Thymidine Phosphorylase Deficiency", "oculogastrointestinal muscular dystrophy", "Myoneurogastrointestinal encephalopathy syndrome", "MYONEUROGASTROINTESTINAL ENCEPHALOPATHY SYNDROME", "myoneurogastrointestinal encephalopathy syndrome", "Mitochondrial Neurogastrointestinal Encephalopathy", "Mitochondrial neurogastrointestinal encephalopathy", "mitochondrial Neurogastrointestingal encephalopathy", "mitochondrial neurogastrointestinal encephalomyopathy", "Mitochondrial neurogastrointestinal encephalomyopathy", "Mitochondrial Neurogastrointestinal Encephalopathy Disease", "MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOPATHY SYNDROME", "Mitochondrial neurogastrointestinal encephalopathy syndrome", "mitochondrial neurogastrointestinal encephalopathy syndrome", "MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOMYOPATHY SYNDROME", "Mitochondrial neurogastrointestinal encephalomyopathy syndrome", "[OBSOLETE] Mitochondrial neurogastrointestinal encephalopathy syndrome", "mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) syndrome", "Mitochondrial neurogastrointestinal encephalomyopathy syndrome (disorder)", "MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOPATHY SYNDROME, TYMP-RELATED", "polyneuropathy, ophthalmoplegia, leukoencephalopathy, and intestinal pseudo-obstruction", "Mitochondrial Myopathy with Sensorimotor Polyneuropathy, Ophthalmoplegia, and Pseudo-Obstruction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial neurogastrointestinal encephalomyopathy", "shortest_name_length": 5}
{"curie": "UMLS:C1377918", "names": ["stage III nasopharynx cancer", "nasopharynx cancer, stage III", "Stage III Nasopharynx Carcinoma", "stage III nasopharyngeal cancer", "nasopharyngeal cancer, stage III", "Stage III Nasopharyngeal Carcinoma", "Stage III Carcinoma of Nasopharynx", "Stage III Nasopharyngeal Throat Cancer", "Stage III Carcinoma of the Nasopharynx", "Stage III Nasopharyngeal Cancer AJCC v6", "Stage III Nasopharynx Carcinoma AJCC v6", "Nasopharyngeal Cancer, Stage III AJCC v6", "Stage III Nasopharyngeal Carcinoma AJCC v6", "Stage III Carcinoma of Nasopharynx AJCC v6", "Stage III Carcinoma of the Nasopharynx AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Nasopharyngeal Carcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0008546", "names": ["TD", "TD1", "PLSD San Diego type", "THANATOPHORIC DWARFISM", "thanatophoric dwarfism", "thanatophoric dysplasia", "THANATOPHORIC DYSPLASIA", "thanatophoric dwarfism 1", "thanatophoric dwarfism type 1", "Thanatophoric dwarfism type 1", "type 1 thanatophoric dysplasia", "thanatophoric dysplasia type 1", "Thanatophoric dysplasia type 1", "Type 1 Thanatophoric Dysplasia", "thanatophoric dysplasia type I", "Thanatophoric Dysplasia, Type 1", "Thanatophoric Dysplasia, Type I", "thanatophoric dysplasia, type 1", "THANATOPHORIC DYSPLASIA, TYPE I", "thanatophoric dysplasia, type I", "Thanatophoric dysplasia, type 1", "Thanatophoric dysplasia, type 1 (disorder)", "Platyspondylic lethal skeletal dysplasia, San Diego type", "Platyspondylic Lethal Skeletal Dysplasia, San Diego Type", "PLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, SAN DIEGO TYPE", "lethal short-limbed Platyspondylic dwarfism, San Diego type", "Lethal Short-Limbed Platyspondylic Dwarfism, San Diego Type", "LETHAL SHORT-LIMBED PLATYSPONDYLIC DWARFISM, SAN DIEGO TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thanatophoric dysplasia type 1", "shortest_name_length": 2}
{"curie": "MONDO:0024417", "names": ["perceptual disorder", "Perceptual Disorder", "perception disorder", "Perceptual disorders", "Perceptual Disorders", "disorders perception", "perceptual disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "perceptual disorders", "shortest_name_length": 19}
{"curie": "MONDO:0011060", "names": ["Age-related nuclear cataract", "CATARACT, AGE-RELATED NUCLEAR", "Nuclear Sclerosis of the Lens", "cataract, age-related nuclear", "nuclear sclerosis of the lens", "Cataract, Age-Related Nuclear", "NUCLEAR SCLEROSIS OF THE LENS", "early-onset non-syndromic cataract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early-onset non-syndromic cataract", "shortest_name_length": 28}
{"curie": "UMLS:C1334955", "names": ["Neuroblastomas of Adrenal Gland and Sympathetic Nervous System", "Neuroblastoma of the Adrenal Gland and Sympathetic Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neuroblastoma of the Adrenal Gland and Sympathetic Nervous System", "shortest_name_length": 62}
{"curie": "MONDO:0001219", "names": ["Serous conjunctivitis, excl viral", "serous conjunctivitis except viral", "Serous conjunctivitis, except viral", "serous conjunctivitis, except viral", "Serous conjunctivitis, excluding viral", "Serous conjunctivitis, except viral (disorder)", "serous conjunctivitis, except viral (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "serous conjunctivitis except viral", "shortest_name_length": 33}
{"curie": "MONDO:0010421", "names": ["XLA", "IMD1", "AGMX1", "bruton disease", "BRUTON DISEASE", "BTK deficiency", "Bruton disease", "BTK-deficiency", "immunodeficiency 1", "IMMUNODEFICIENCY 1", "Immunodeficiency 1", "Agammaglobulinemia, BTK", "agammaglobulinemia, BTK", "Bruton; agammaglobulinemia", "agammaglobulinemia; Bruton", "agammaglobulinemia x-linked", "Bruton's Agammaglobulinemia", "X-Linked Agammaglobulinemia", "x-linked agammaglobulinemia", "bruton's agammaglobulinemia", "X linked agammaglobulinemia", "agammaglobulinemia X-linked", "X-linked agammaglobulinemia", "Bruton's agammaglobulinemia", "Bruton's agammaglobulinaemia", "X-linked agammaglobulinaemia", "X linked agammaglobulinaemia", "agammaglobulinemia; X-linked", "agammaglobulinemia, X-linked", "X-linked; agammaglobulinemia", "AGAMMAGLOBULINEMIA, X-LINKED", "Agammaglobulinemia, X-Linked", "CONGENITAL AGAMMAGLOBULINEMIA", "Congenital Agammaglobulinemia", "agammaglobulinemia (X-linked)", "sex-linked agammaglobulinemia", "Congenital agammaglobulinemia", "X-linked hypogammaglobulinemia", "Bruton-type agammaglobulinemia", "Bruton type agammaglobulinemia", "Bruton's hypogammaglobulinemia", "hypogammaglobulinemia x-linked", "AGAMMAGLOBULINEMIA, CONGENITAL", "Bruton-Type Agammaglobulinemia", "BRUTON-TYPE AGAMMAGLOBULINEMIA", "AGAMMAGLOBULINEMIA, SEX-LINKED", "hypogammaglobulinemia, X-linked", "Bruton's hypogammaglobulinaemia", "Hypogammaglobulinemia, X-Linked", "HYPOGAMMAGLOBULINEMIA, X-LINKED", "X-linked hypogammaglobulinaemia", "Bruton's type agammaglobulinemia", "XLA - X-linked agammaglobulinemia", "Bruton's type agammaglobulinaemia", "XLA - X-linked agammaglobulinaemia", "Bruton; X-linked agammaglobulinemia", "AGAMMAGLOBULINEMIA, X-LINKED, TYPE 1", "Agammaglobulinemia, X-Linked, Type I", "agammaglobulinemia, X-linked, type 1", "Bruton's X-linked agammaglobulinemia", "Bruton's X-Linked Agammaglobulinemia", "Infantile X-linked agammaglobulinemia", "X-linked agammaglobulinemia (disorder)", "Bruton's Sex-linked agammaglobulinemia", "Bruton's Sex-Linked Agammaglobulinemia", "AGAMMAGLOBULINEMIA, X-LINKED INFANTILE", "X-linked agammaglobulinemia (diagnosis)", "X-linked hypogammaglobulinemia (diagnosis)", "agammaglobulinemia, Bruton tyrosine kinase", "Agammaglobulinemia, Bruton tyrosine kinase", "Bruton's type agammaglobulinemia (diagnosis)", "agammaglobulinemia, X-linked 1, X-linked recessive", "Bruton-type (congenital X-linked) agammaglobulinemia", "Bruton agammaglobulinemia tyrosine kinase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bruton-type agammaglobulinemia", "shortest_name_length": 3}
{"curie": "MONDO:0043373", "names": ["sudden deafness", "deafness, sudden", "sudden hear loss", "Sudden Hearing Loss", "hearing loss sudden", "Sudden hearing loss", "sudden hearing loss", "Hearing Loss, Sudden", "sudden loss of hearing", "Sudden hearing loss NOS", "Sudden hearing loss, NOS", "Sudden hearing loss (disorder)", "Sudden hearing loss, unspecified", "sudden loss of hearing (symptom)", "sudden sensorineural hearing loss", "Sudden sensorineural hearing loss", "Sudden sensorineural hearing loss (disorder)", "sudden sensorineural hearing loss (diagnosis)", "acute sensorineural hearing loss by acute acoustic trauma or sudden deafness or surgery induced acoustic trauma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sudden sensorineural hearing loss", "shortest_name_length": 15}
{"curie": "MONDO:0017200", "names": ["FOWLER SYNDROME", "Fowler syndrome", "Fowler's syndrome", "fowler's syndrome", "Fowler syndrome (disorder)", "fowler Christmas Chapple syndrome", "Fowler-Christmas-Chapple syndrome", "Fowler Christmas Chapple syndrome", "fowler-Christmas-Chapple syndrome", "voiding dysfunction and polycystic ovaries", "Voiding dysfunction, and polycystic ovaries", "Fowler urethral sphincter dysfunction syndrome", "polycystic ovaries urethral sphincter dysfunction", "polycystic ovaries-urethral sphincter dysfunction syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polycystic ovaries-urethral sphincter dysfunction syndrome", "shortest_name_length": 15}
{"curie": "UMLS:C1332519", "names": ["Benign Nipple Tumor", "Benign nipple neoplasm", "Benign Nipple Neoplasm", "Benign Tumor of Nipple", "Benign Neoplasm of Nipple", "Benign Tumor of the Nipple", "Benign Neoplasm of the Nipple"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign nipple neoplasm", "shortest_name_length": 19}
{"curie": "MONDO:0007024", "names": ["Pseudotuberculosis", "pseudotuberculosis", "Rodent pseudotuberculosis", "Pseudotuberculosis (disorder)", "pseudotuberculosis (diagnosis)", "Pasteurella pseudotuberculosis", "Pasteurella Pseudotuberculosis", "Pasteurella Pseudotuberculoses", "pseudotuberculosis, Pasteurella", "Pseudotuberculoses, Pasteurella", "Pseudotuberculosis, Pasteurella", "Yersinia pseudotuberculosis infection", "Yersinia pseudotuberculosis Infections", "Yersinia pseudotuberculosis; infection", "infection; Yersinia pseudotuberculosis", "Infections, Yersinia pseudotuberculosis", "infections, Yersinia pseudotuberculosis", "Pasteurella pseudotuberculosis infection", "Infection by Yersinia pseudotuberculosis", "infection by Yersinia pseudotuberculosis", "Infection by Pasteurella pseudotuberculosis", "infection by Pasteurella pseudotuberculosis", "Yersinia pseudotuberculosis infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Yersinia pseudotuberculosis infectious disease", "shortest_name_length": 18}
{"curie": "MONDO:0016990", "names": ["Acquired hypoprothrombinemia", "acquired hypoprothrombinemia", "Hypoprothrombinemia, acquired", "hypoprothrombinemia, acquired", "Acquired Factor II Deficiency", "Acquired factor II deficiency", "acquired factor II deficiency", "Acquired hypoprothrombinaemia", "acquired prothrombin deficiency", "Acquired prothrombin deficiency", "prothrombin; deficiency, acquired", "Acquired hypoprothrombinemia, NOS", "deficiency; prothrombin, acquired", "Acquired factor II deficiency disease", "Acquired factor II deficiency (disorder)", "acquired hypoprothrombinemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired prothrombin deficiency", "shortest_name_length": 28}
{"curie": "MONDO:0032889", "names": ["POBINDS", "Poirier-Bienvenu neurodevelopmental syndrome", "POIRIER-BIENVENU NEURODEVELOPMENTAL SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Poirier-Bienvenu neurodevelopmental syndrome", "shortest_name_length": 7}
{"curie": "UMLS:C4525857", "names": ["Stage IIIB Colon Neuroendocrine Tumor", "Stage IIIB Colon Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Colon Neuroendocrine Tumor AJCC v8", "shortest_name_length": 37}
{"curie": "MONDO:0100193", "names": ["ESLD", "Chronic Liver Failure", "Chronic liver failure", "chronic liver failure", "Liver Failure, Chronic", "Chronic Liver Failures", "Failure, Chronic Liver", "chronic hepatic failure", "end-stage liver disease", "HEPATIC FAILURE CHRONIC", "end stage liver disease", "End stage liver disease", "End-Stage Liver Disease", "End Stage Liver Disease", "Chronic hepatic failure", "Liver Failures, Chronic", "Failures, Chronic Liver", "liver disease end stage", "LIVER DISEASE END STAGE", "disease end liver stage", "disease end liver stages", "end stage hepatic failure", "HEPATIC FAILURE END STAGE", "insufficiency; hepatic, chronic", "Chronic hepatic failure (disorder)", "End stage liver disease (disorder)", "chronic hepatic failure (diagnosis)", "end stage hepatic failure (diagnosis)", "End Stage Liver Disease (Decompensated Liver Disease)", "end stage liver disease (decompensated liver disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic liver failure", "shortest_name_length": 4}
{"curie": "MONDO:0005907", "names": ["Gulf War Syndrome", "gulf syndrome war", "Gulf war syndrome", "gulf war syndrome", "Syndrome, Gulf War", "Persian Gulf Syndrome", "persian gulf syndrome", "Persian Gulf syndrome", "Gulf war syndrome, NOS", "Syndrome, Persian Gulf", "Persian Gulf war syndrome", "Gulf war syndrome (disorder)", "Persian Gulf war syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "persian gulf syndrome", "shortest_name_length": 17}
{"curie": "UMLS:C5555053", "names": ["EWSR1-PATZ1 Sarcoma", "EWSR1::PATZ1 Sarcoma", "Round Cell Sarcoma with EWSR1-PATZ1 Gene Fusion", "Round Cell Sarcoma with EWSR1::PATZ1 Gene Fusion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Round Cell Sarcoma with EWSR1-PATZ1 Gene Fusion", "shortest_name_length": 19}
{"curie": "UMLS:C4289316", "names": ["FIGO Stage IIIA1(ii) Ovarian Cancer", "FIGO Stage IIIA1(ii) Ovarian Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Stage IIIA1(ii) Ovarian Cancer", "shortest_name_length": 35}
{"curie": "MONDO:0009860", "names": ["phenformin 4-hydroxylation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phenformin 4-hydroxylation", "shortest_name_length": 26}
{"curie": "MONDO:0700028", "names": ["chromosome Y disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome Y disorder", "shortest_name_length": 21}
{"curie": "UMLS:C0456876", "names": ["Low Grade T-Cell Lymphoma", "Low grade T-cell lymphoma", "Low grade T-cell lymphoma (disorder)", "Low grade T-cell lymphoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low grade T-cell lymphoma", "shortest_name_length": 25}
{"curie": "UMLS:C0001819", "names": ["Agoraphobia without mention of panic attacks", "Agoraphobia without mention of panic disorder", "Agoraphobia without history of panic disorder", "agoraphobia without history of panic disorder", "Agoraphobia without a History of Panic Disorder", "Agoraphobia without a history of panic disorder", "Agoraphobia without history of panic disorder, NOS", "Agoraphobia without history of panic disorder (disorder)", "agoraphobia without history of panic disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Agoraphobia without history of panic disorder", "shortest_name_length": 44}
{"curie": "MONDO:0033369", "names": ["DEE60", "EIEE60", "early infantile epileptic encephalopathy 60", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 60", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 60", "developmental and epileptic encephalopathy 60", "epileptic encephalopathy, early infantile, 60", "developmental and epileptic encephalopathy, 60"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 60", "shortest_name_length": 5}
{"curie": "UMLS:C1707827", "names": ["Ductal Eccrine Carcinoma with Abundant Fibromyxoid Stroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ductal Eccrine Carcinoma with Abundant Fibromyxoid Stroma", "shortest_name_length": 57}
{"curie": "MONDO:0004498", "names": ["Sacral Intraspinal Meningioma", "sacral intraspinal meningioma", "sacral spinal canal and spinal cord meningioma", "Sacral Spinal Canal and Spinal Cord Meningioma", "meningioma of sacral spinal canal and spinal cord", "Meningioma of Sacral Spinal Canal and Spinal Cord", "meningioma of the sacral spinal canal and spinal cord", "meningioma of the Sacral Spinal canal and Spinal Cord", "Meningioma of the Sacral Spinal Canal and Spinal Cord"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sacral spinal canal and spinal cord meningioma", "shortest_name_length": 29}
{"curie": "MONDO:0003645", "names": ["face cavernous hemangioma", "cavernous hemangioma of face", "Cavernous Hemangioma of Face", "Cavernous Hemangioma of the Face", "Cavernous hemangioma of the face", "cavernous hemangioma of the Face"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cavernous hemangioma of face", "shortest_name_length": 25}
{"curie": "MONDO:0009580", "names": ["MRT1", "Mental Retardation, Autosomal Recessive 1", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 1", "mental retardation, autosomal recessive 1", "intellectual disability, autosomal recessive 1", "mental retardation, autosomal recessive type 1", "intellectual disability, autosomal recessive type 1", "autosomal recessive intellectual developmental disorder 1", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 1", "PRSS12 autosomal recessive non-syndromic intellectual disability", "autosomal recessive non-syndromic intellectual disability caused by mutation in PRSS12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 1", "shortest_name_length": 4}
{"curie": "UMLS:C0238258", "names": ["LUNG, LYMPHANGITIC CANCER", "Lymphangitis carcinomatosa", "lymphangitis carcinomatosa", "LYMPHANGITIS CARCINOMATOSIS", "lymphangitis carcinomatosis", "Lymphangitis carcinomatosis", "lymphangitic carcinomatosis", "Lymphangitic Carcinomatosis", "LYMPHANGITIC CARCINOMATOSIS", "LYMPHANGITIC METASTATIC DISEASE", "Lymphangitis carcinomatosa (disorder)", "lymphangitis carcinomatosa (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphangitis carcinomatosa", "shortest_name_length": 25}
{"curie": "UMLS:C0751855", "names": ["Hatter's shakes", "mercury encephalopathy", "Mercury Encephalopathy", "Encephalopathy, Mercury", "Encephalopathy due to mercury", "Encephalopathy caused by mercury", "Toxic encephalitis due to mercury", "mercury encephalopathy (diagnosis)", "Toxic encephalopathy due to mercury", "Toxic encephalopathy caused by mercury", "Toxic encephalopathy caused by mercury (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mercury Encephalopathy", "shortest_name_length": 15}
{"curie": "MONDO:0032795", "names": ["MRD59", "intellectual developmental disorder 59", "INTELLECTUAL DEVELOPMENTAL DISORDER 59", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 59", "Mental Retardation, Autosomal Dominant 59", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 59"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder 59", "shortest_name_length": 5}
{"curie": "MONDO:0005358", "names": ["DHF", "dengue hemorrhagic fever", "Dengue hemorrhagic fever", "Dengue Hemorrhagic Fever", "Dengue haemorrhagic fever"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dengue hemorrhagic fever", "shortest_name_length": 3}
{"curie": "UMLS:C0280184", "names": ["intermediate-grade, relapsed adult NHL", "relapsed adult NHL, intermediate grade", "recurrent adult NHL, intermediate grade", "adult NHL, relapsed, intermediate grade", "NHL, intermediate grade, relapsed adult", "intermediate-grade, recurrent adult NHL", "NHL, intermediate grade, recurrent adult", "adult NHL, recurrent, intermediate grade", "intermediate-grade, relapsed adult non-Hodgkin's lymphoma", "Recurrent Intermediate Grade Adult Non-Hodgkin's Lymphoma", "relapsed adult non-Hodgkin's lymphoma, intermediate grade", "non-Hodgin's lymphoma intermediate grade, recurrent adult", "recurrent adult non-Hodgkin's lymphoma, intermediate grade", "adult non-Hodgkin's lymphoma, intermediate grade, relapsed", "non-Hodgkin's lymphoma, intermediate grade, relapsed adult", "adult non-Hodgkin's lymphoma, intermediate grade, recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Intermediate Grade Adult Non-Hodgkin's Lymphoma", "shortest_name_length": 38}
{"curie": "UMLS:C2983707", "names": ["Rectal Cancer by AJCC v6 Stage", "Rectal Carcinoma by AJCC v6 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rectal Cancer by AJCC v6 Stage", "shortest_name_length": 30}
{"curie": "UMLS:C1370913", "names": ["Borderline Phyllodes Tumor", "Borderline phyllodes tumor", "Borderline phyllodes tumour", "Phyllodes tumor, borderline", "Phyllodes tumour, borderline", "Borderline Phyllodes Neoplasm", "Borderline cystosarcoma phyllodes", "Borderline phyllodes tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline phyllodes tumor", "shortest_name_length": 26}
{"curie": "MONDO:0013602", "names": ["PGL5", "PARAGANGLIOMAS 5", "paragangliomas 5", "SDHA paraganglioma", "paragangliomas type 5", "paraganglioma caused by mutation in SDHA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paragangliomas 5", "shortest_name_length": 4}
{"curie": "UMLS:C1721017", "names": ["Paraneoplastic Opsoclonus-Myoclonus Ataxia", "Paraneoplastic Opsoclonus Myoclonus Ataxia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paraneoplastic Opsoclonus-Myoclonus Ataxia", "shortest_name_length": 42}
{"curie": "MONDO:0006145", "names": ["Chondroid Chordoma", "Chondroid chordoma", "chondroid chordoma", "chondroid chordoma (diagnosis)", "chondroid chordoma (morphologic abnormality)", "Chondroid chordoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chondroid chordoma", "shortest_name_length": 18}
{"curie": "MONDO:0016771", "names": ["Annular atrophic LP", "annular atrophic LP", "annular atrophic lichen planus", "Annular atrophic lichen planus", "Annular atrophic lichen planus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "annular atrophic lichen planus", "shortest_name_length": 19}
{"curie": "MONDO:0037738", "names": ["cauda equina cancer", "cancer of cauda equina", "malignant cauda equina neoplasm", "malignant neoplasm of cauda equina", "Malignant neoplasm of cauda equina", "Malignant neoplasm of cauda equina (disorder)", "malignant neoplasm of cauda equina (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cauda equina cancer", "shortest_name_length": 19}
{"curie": "UMLS:C1333552", "names": ["FIGO Stage IIA GTT", "FIGO Stage IIA Gestational Trophoblastic Tumor", "FIGO Stage IIA Gestational Trophoblastic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Stage IIA Gestational Trophoblastic Tumor", "shortest_name_length": 18}
{"curie": "MONDO:0011196", "names": ["ALS5", "ALS5 (diagnosis)", "AMYOTROPHIC LATERAL SCLEROSIS 5", "amyotrophic lateral sclerosis 5", "Amyotrophic Lateral Sclerosis 5", "amyotrophic lateral sclerosis ALS5", "SPG11 amyotrophic lateral sclerosis", "amyotrophic lateral sclerosis type 5", "amyotrophic lateral sclerosis 5, juvenile", "AMYOTROPHIC LATERAL SCLEROSIS 5, JUVENILE", "amyotrophic lateral sclerosis caused by mutation in SPG11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyotrophic lateral sclerosis type 5", "shortest_name_length": 4}
{"curie": "UMLS:C0238032", "names": ["breast hamartoma", "Breast Hamartoma", "Breast hamartoma", "BREAST, HAMARTOMA", "Breast fibroadenolipoma", "BREAST, FIBROADENOLIPOMA", "BREAST, POSTLACTATIONAL TUMOR"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast fibroadenolipoma", "shortest_name_length": 16}
{"curie": "UMLS:C1336405", "names": ["Stage IVC Mouth Verrucous Carcinoma", "Stage IVC Verrucous Carcinoma of Mouth", "Stage IVC Oral Cavity Verrucous Cancer", "Stage IVC Oral Cavity Verrucous Carcinoma", "Stage IVC Verrucous Carcinoma of the Mouth", "Stage IVC Verrucous Carcinoma of Oral Cavity", "Stage IVC Verrucous Carcinoma of the Oral Cavity", "stage IVC verrucous carcinoma of the oral cavity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Oral Cavity Verrucous Carcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C0751953", "names": ["Posterior Circulation Brain Infarction", "Posterior Circulation Infarction, Brain", "Brain Infarction, Posterior Circulation", "Infarction, Posterior Circulation, Brain", "Infarction, Brain, Posterior Circulation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brain Infarction, Posterior Circulation", "shortest_name_length": 38}
{"curie": "UMLS:C4087137", "names": ["Needle fatigue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Needle fatigue", "shortest_name_length": 14}
{"curie": "MONDO:0003392", "names": ["Fallopian Tube Germ Cell Tumor", "fallopian tube germ cell tumor", "fallopian tube germ cell cancer", "fallopian tube germ cell neoplasm", "Fallopian Tube Germ Cell Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fallopian tube germ cell tumor", "shortest_name_length": 30}
{"curie": "MONDO:0042911", "names": ["Schwartz-Cohen-addad-Lambert syndrome", "Schwartz Cohen-Addad Lambert syndrome", "Congenital melanocytosis with myelomeningocele and hydrocephalus", "congenital melanocytosis with myelomeningocele and hydrocephalus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Schwartz-Cohen-addad-Lambert syndrome", "shortest_name_length": 37}
{"curie": "UMLS:C2987269", "names": ["Esophageal MALT Lymphoma", "Esophageal Mucosa-Associated Lymphoid Tissue Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Mucosa-Associated Lymphoid Tissue Lymphoma", "shortest_name_length": 24}
{"curie": "UMLS:C0920569", "names": ["liver ischemia", "Hepatic ischemia", "hepatic ischemia", "Hepatic ischaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatic ischemia", "shortest_name_length": 14}
{"curie": "MONDO:0009474", "names": ["isovaleric acid, inability to smell", "ISOVALERIC ACID, INABILITY TO SMELL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isovaleric acid, inability to smell", "shortest_name_length": 35}
{"curie": "MONDO:0040503", "names": ["BCDS2", "blepharocheilodontic syndrome 2", "BLEPHAROCHEILODONTIC SYNDROME 2", "BLEPHAROCHEILODONTIC syndrome 2", "CTNND1 blepharo-cheilo-odontic syndrome", "blepharo-cheilo-odontic syndrome caused by mutation in CTNND1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blepharocheilodontic syndrome 2", "shortest_name_length": 5}
{"curie": "UMLS:C2983708", "names": ["Rectosigmoid Cancer by AJCC v6 Stage", "Rectosigmoid Carcinoma by AJCC v6 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rectosigmoid Cancer by AJCC v6 Stage", "shortest_name_length": 36}
{"curie": "UMLS:C1708667", "names": ["Leaflet Disruption Due To Calcification"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leaflet Disruption Due To Calcification", "shortest_name_length": 39}
{"curie": "UMLS:C5237459", "names": ["Refractory T-MF", "Refractory Transformed Mycosis Fungoides"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Transformed Mycosis Fungoides", "shortest_name_length": 15}
{"curie": "UMLS:C1333564", "names": ["FIGO Stage I GTT", "FIGO Stage I Gestational Trophoblastic Tumor", "FIGO Stage I Gestational Trophoblastic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Stage I Gestational Trophoblastic Tumor", "shortest_name_length": 16}
{"curie": "MONDO:0004720", "names": ["Amaas", "milkpox", "alastrim", "Alastrim", "whitepox", "cottonpox", "Kaffir pox", "Variola minor", "Variola Minor", "variola minor", "Minor, Variola", "Variola Minors", "Minors, Variola", "Alastrim (disorder)", "alastrim (diagnosis)", "variola minor infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "variola minor infection", "shortest_name_length": 5}
{"curie": "MONDO:0014031", "names": ["ALAZS", "Alazami syndrome", "ALAZAMI SYNDROME", "Microcephalic primordial dwarfism Alazami type", "microcephaly primordial dwarfism, Alazami type", "Microcephalic primordial dwarfism, Alazami type", "microcephalic primordial dwarfism, Alazami type", "Microcephalic primordial dwarfism Alazami type (disorder)", "microcephaly primordial dwarfism, Alazami type (diagnosis)", "FACIAL DYSMORPHISM, INTELLECTUAL DISABILITY, AND PRIMORDIAL DWARFISM", "facial dysmorphism, intellectual disability, and primordial dwarfism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephalic primordial dwarfism, Alazami type", "shortest_name_length": 5}
{"curie": "MONDO:0012884", "names": ["SLEB13", "systemic lupus erythematosus, susceptibility to, 13", "SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 13"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "systemic lupus erythematosus, susceptibility to, 13", "shortest_name_length": 6}
{"curie": "UMLS:C0156231", "names": ["Chronic Glomerulonephritis with Lesion of Proliferative Glomerulonephritis", "Chronic glomerulonephritis with lesion of proliferative glomerulonephritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic glomerulonephritis with lesion of proliferative glomerulonephritis", "shortest_name_length": 74}
{"curie": "UMLS:C1336153", "names": ["Stage IIA Adenosquamous Lung Cancer", "Stage IIA Adenosquamous Lung Carcinoma", "Stage IIA Adenosquamous Cell Lung Carcinoma", "Stage IIA Adenosquamous Cell Carcinoma of Lung", "Stage IIA Lung Adenosquamous Carcinoma AJCC v7", "Stage IIA Adenosquamous Cell Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Lung Adenosquamous Carcinoma AJCC v7", "shortest_name_length": 35}
{"curie": "UMLS:C0854135", "names": ["Pseudomonas; aeruginosa", "aeruginosa; Pseudomonas", "Pseudomonas aeruginosa infection", "pseudomonas aeruginosa infection", "Infection Pseudomonas aeruginosa", "aeruginosa infections pseudomona", "Pseudomonas aeruginosa Infection", "Pseudomonas aeruginosa Infections", "aeruginosa infections pseudomonas", "Pseudomonas aeruginosa infection NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pseudomonas aeruginosa infection", "shortest_name_length": 23}
{"curie": "MONDO:0100449", "names": ["PCARP", "AXPC1", "FLVCR1 retinopathy with or without ataxia", "posterior column ataxia with retinitis pigmentosa", "FLVCR1-related retinopathy with or without ataxia", "ataxia, posterior column, with retinitis pigmentosa", "posterior column ataxia-retinitis pigmentosa syndrome", "autosomal recessive posterior column ataxia and retinitis pigmentosa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FLVCR1-related retinopathy with or without ataxia", "shortest_name_length": 5}
{"curie": "MONDO:0006573", "names": ["lipoatrophy", "Lipodystrophy", "LIPODYSTROPHY", "lipodystrophy", "Lipodystrophies", "Lipodystrophy NOS", "Lipodystrophy, NOS", "CUTANEOUS LIPODYSTROPHY", "lipodystrophy (disease)", "Dystrophy, fatty tissue", "lipodsystrophic syndrome", "Lipodystrophy (disorder)", "Lipodsystrophic Syndromes", "lipodsystrophic syndromes", "lipodystrophy (diagnosis)", "Dystrophy of fatty tissue", "Inability to make and keep healthy fat tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lipodystrophy", "shortest_name_length": 11}
{"curie": "MONDO:0010729", "names": ["SCHIMKE X-LINKED MENTAL RETARDATION SYNDROME", "Schimke X-linked mental retardation syndrome", "X-linked intellectual disability Schimke type", "X-linked intellectual disability, Schimke type", "choreoathetosis with mental retardation X- linked", "choreoathetosis with mental retardation, X-linked", "Schimke X-linked intellectual disability syndrome", "Choreoathetosis With Mental Retardation, X-Linked", "CHOREOATHETOSIS WITH MENTAL RETARDATION, X-LINKED", "Choreoathetosis with mental retardation X- linked", "choreoathetosis with intellectual disability, X-linked", "choreoathetosis with intellectual disability X- linked", "X-linked intellectual disability Schimke type (disorder)", "X-linked intellectual disability Schimke type (diagnosis)", "progressive basal ganglion dysfunction, mental and growth retardation, external ophthalmoplegia, postnatal microcephaly and deafness", "Progressive basal ganglion dysfunction, mental and growth retardation, external ophthalmoplegia, postnatal microcephaly and deafness", "childhood-onset choreoathetosis with spasticity, postnatal microcephaly, growth and mental retardation, ophthalmoplegia, and deafness", "Childhood-onset choreoathetosis with spasticity, postnatal microcephaly, growth and mental retardation, ophthalmoplegia, and deafness", "childhood-onset choreoathetosis with spasticity, postnatal microcephaly, growth and intellectual disability, ophthalmoplegia, and deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability, Schimke type", "shortest_name_length": 44}
{"curie": "UMLS:C5555771", "names": ["Mesenteric Calcifying Fibrous Tumor", "Peritoneal Calcifying Fibrous Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peritoneal Calcifying Fibrous Tumor", "shortest_name_length": 35}
{"curie": "UMLS:C0153734", "names": ["Hodgkin's paragranuloma, spleen", "Hodgkin's paragranuloma of spleen", "Hodgkin lymphoma paragranuloma of spleen", "Hodgkin's paragranuloma involving spleen", "Hodgkin's Paragranuloma Involving Spleen", "Hodgkin lymphoma paragranuloma of spleen (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's Paragranuloma Involving Spleen", "shortest_name_length": 31}
{"curie": "MONDO:0022236", "names": ["colpocephaly", "Colpocephaly", "Colpocephaly (disorder)", "colpocephaly (diagnosis)", "congenital malformation brain colpocephaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colpocephaly", "shortest_name_length": 12}
{"curie": "MONDO:0024622", "names": ["ADENOCARCINOMA THYROID", "Thyroid adenocarcinoma", "Adenocarcinoma thyroid", "Thyroid Adenocarcinoma", "thyroid adenocarcinoma", "THYROID, ADENOCARCINOMA", "Adenocarcinoma of thyroid", "thyroid gland adenocarcinoma", "Thyroid Gland Adenocarcinoma", "Adenocarcinoma of thyroid gland", "adenocarcinoma of thyroid gland", "thyroid adenocarcinoma (diagnosis)", "Adenocarcinoma of thyroid gland (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid gland adenocarcinoma", "shortest_name_length": 22}
{"curie": "MONDO:0000936", "names": ["Meningeal syphilis", "meningeal syphilis", "syphilitic meningitis", "Syphilitic meningitis", "Meningitis, syphilitic", "meningitis, syphilitic", "meningeal neurosyphilis", "syphilitic aseptic meningitis", "Syphilitic aseptic meningitis", "Treponema infectious meningitis", "Syphilitic meningitis (disorder)", "meningeal neurosyphilis (diagnosis)", "Treponema caused infectious meningitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syphilitic meningitis", "shortest_name_length": 18}
{"curie": "MONDO:0032899", "names": ["SCN8", "SDSL", "Shwachman-Diamond Syndrome-Like", "Shwachman-Diamond syndrome-like", "severe congenital neutropenia 8", "SHWACHMAN-DIAMOND SYNDROME-LIKE", "neutropenia, severe congenital, 8, autosomal dominant", "NEUTROPENIA, SEVERE CONGENITAL, 8, AUTOSOMAL DOMINANT", "autosomal dominant severe congenital neutropenia 8 with or without pancreatic dysfunction and/or neurological abnormalities", "Neutropenia, Severe Congenital, 8, Autosomal Dominant, With or Without Pancreatic Dysfunction And/Or Neurologic Abnormalities", "NEUTROPENIA, SEVERE CONGENITAL, 8, AUTOSOMAL DOMINANT, WITH OR WITHOUT PANCREATIC DYSFUNCTION AND/OR NEUROLOGIC ABNORMALITIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neutropenia, severe congenital, 8, autosomal dominant", "shortest_name_length": 4}
{"curie": "UMLS:C3838825", "names": ["ACT", "Chondrosarcoma, grade 1", "Atypical cartilaginous tumor", "Atypical Cartilaginous Tumor", "Atypical cartilaginous tumour", "Atypical cartilaginous tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypical cartilaginous tumor", "shortest_name_length": 3}
{"curie": "MONDO:0019811", "names": ["tricuspid valve agenesis", "congenital unguarded tricuspid orifice"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tricuspid valve agenesis", "shortest_name_length": 24}
{"curie": "UMLS:C3872606", "names": ["recurrent vaginal candidiasis", "candidiasis vaginal recurrent", "Recurrent candidiasis of vagina", "recurrent vaginal candidiasis (diagnosis)", "Recurrent candidiasis of vagina (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent candidiasis of vagina", "shortest_name_length": 29}
{"curie": "MONDO:0003864", "names": ["CLL/SLL", "B-cell lymphocytic leukemia/small lymphocytic lymphoma", "Chronic lymphocytic leukemia/small lymphocytic lymphoma", "chronic lymphocytic leukemia/small lymphocytic lymphoma", "Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma", "chronic lymphocytic leukemia/small lymphocytic lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic lymphocytic leukemia/small lymphocytic lymphoma", "shortest_name_length": 7}
{"curie": "MONDO:0009194", "names": ["CEBV", "IMD32B", "CAEBV syndrome", "CAEBV infection", "immunodeficiency 32B", "IMMUNODEFICIENCY 32B", "chronic EBV infection syndrome", "chronic active Epstein-Barr disease", "autosomal recessive IRF8 deficiency", "IRF8 DEFICIENCY, AUTOSOMAL RECESSIVE", "IRF8 deficiency, autosomal recessive", "chronic active Epstein-Barr virus infection", "chronic Epstein-Barr virus infection syndrome", "EPSTEIN-BARR VIRUS, SUSCEPTIBILITY TO CHRONIC INFECTION BY", "Epstein-Barr VIRUS, susceptibility to chronic infection by", "monocyte and dendritic cell deficiency, autosomal recessive", "immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive", "immunodeficiency 32B, monocyte, Dendritic cell, and natural Killer cell deficiency, autosomal recessive", "IMMUNODEFICIENCY 32B, MONOCYTE, DENDRITIC CELL, AND NATURAL KILLER CELL DEFICIENCY, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 32B", "shortest_name_length": 4}
{"curie": "UMLS:C0271629", "names": ["MIS Deficiency", "Mullerian Inhibiting Factor Deficiency", "Mullerian inhibiting factor deficiency", "Mullerian regression factor deficiency", "Müllerian Inhibiting Factor Deficiency", "Mullerian Inhibiting Substance Deficiency", "Müllerian Inhibiting Substance Deficiency", "Mullerian inhibiting factor deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mullerian inhibiting factor deficiency", "shortest_name_length": 14}
{"curie": "MONDO:0032612", "names": ["MC1DN7", "nuclear type mitochondrial complex I deficiency 7", "mitochondrial complex 1 deficiency, nuclear type 7", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 7", "shortest_name_length": 6}
{"curie": "UMLS:C0751120", "names": ["Neonatal myoclonic epilepsy", "Myoclonic epilepsy of infancy", "Benign Infantile Myoclonic Epilepsy", "Benign myoclonic epilepsy in infancy", "Myoclonic Epilepsy, Benign Infantile", "benign myoclonic epilepsy in infancy", "Benign myoclonus epilepsy of infancy", "Benign myoclonic epilepsy of infancy", "Myoclonic Epilepsy, Infantile, Benign", "Epilepsy, Myoclonic, Infantile, Benign", "myoclonic; epileptic, benign, of infancy", "Benign myoclonic epilepsy in infancy (disorder)", "benign myoclonic epilepsy in infancy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Infantile Myoclonic Epilepsy", "shortest_name_length": 27}
{"curie": "MONDO:0014057", "names": ["MSUDMV", "maple syrup urine disease, mild variant", "MAPLE SYRUP URINE DISEASE, MILD VARIANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maple syrup urine disease, mild variant", "shortest_name_length": 6}
{"curie": "UMLS:C0855190", "names": ["Stage III Bladder Squamous Cell Cancer", "Bladder squamous cell carcinoma stage III", "Squamous cell bladder carcinoma stage III", "Stage III Bladder Squamous Cell Carcinoma", "Squamous cell carcinoma of the bladder stage III", "Stage III Bladder Squamous Cell Carcinoma AJCC v6", "Stage III Bladder Squamous Cell Carcinoma AJCC v7", "Stage III Bladder Squamous Cell Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder squamous cell carcinoma stage III", "shortest_name_length": 38}
{"curie": "MONDO:0008123", "names": ["OMOD2", "omodysplasia 2", "Omodysplasia 2", "OMODYSPLASIA 2", "autosomal dominant omodysplasia", "Autosomal dominant omodysplasia", "omodysplasia, autosomal dominant", "OMODYSPLASIA, AUTOSOMAL DOMINANT", "Omodysplasia, Autosomal Dominant", "Autosomal dominant omodysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant omodysplasia", "shortest_name_length": 5}
{"curie": "MONDO:0020125", "names": ["acquired neuromuscular junction disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired neuromuscular junction disease", "shortest_name_length": 39}
{"curie": "MONDO:0017517", "names": ["short toes, unilateral", "brachydactyly of toes, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly of toes, unilateral", "shortest_name_length": 22}
{"curie": "MONDO:0022622", "names": ["CDG syndrome type 4", "congenital disorder of glycosylation syndrome type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital disorder of glycosylation syndrome type 4", "shortest_name_length": 19}
{"curie": "UMLS:C5204067", "names": ["Locally Advanced Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Neuroendocrine Carcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0014474", "names": ["MDDGC7", "LGMD2U", "LGMDR20", "LGMD type 2U", "ISPD-related LGMD R20", "muscular dystrophy limb-girdle type 2U", "Limb-girdle muscular dystrophy type 2U", "muscular dystrophy, limb-girdle, type 2U", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2U", "ISPD-related limb-girdle muscular dystrophy R20", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 20", "ISPD autosomal recessive limb-girdle muscular dystrophy", "Autosomal recessive limb-girdle muscular dystrophy type 2U", "autosomal recessive limb-girdle muscular dystrophy type 2U", "Autosomal recessive limb girdle muscular dystrophy type 2U", "muscular dystrophy-dystroglycanopathy (limb-girdle) type C7", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7", "muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 7", "LGMD2U - autosomal recessive limb girdle muscular dystrophy type 2U", "Autosomal recessive limb girdle muscular dystrophy type 2U (disorder)", "Autosomal recessive limb girdle muscular dystrophy due to ISPD deficiency", "autosomal recessive limb-girdle muscular dystrophy due to ISPD deficiency", "autosomal recessive limb-girdle muscular dystrophy caused by mutation in ISPD"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive limb-girdle muscular dystrophy type 2U", "shortest_name_length": 6}
{"curie": "MONDO:0020696", "names": ["Hypocobalaminemia", "hypocobalaminemia", "Hypocobalaminaemia", "cobalamin deficiency", "deficiency cobalamin", "Cobalamin deficiency", "Deficiency;vitamin B12", "VITAMIN B12 DEFICIENCY", "deficiency vitamin b12", "b12 vitamin deficiency", "b12 deficiency vitamin", "vitamin b12 deficiency", "Vitamin B12 Deficiency", "vitamin B12 deficiency", "Vitamin B12 deficiency", "Deficiency, Vitamin B12", "Vitamin B 12 Deficiency", "b12 deficiency vitamins", "VITAMIN B 12 DEFICIENCY", "vitamin b 12 deficiency", "deficiency; vitamin, B12", "Vitamin B12 Deficiencies", "Deficiency, Vitamin B 12", "vitamin; deficiency, B12", "vitamin b12 deficiencies", "deficiency of vitamin b12", "of vitamin b12 deficiency", "Cyanocobalamin deficiency", "Deficiency of vitamin B12", "CYANOCOBALAMIN DEFICIENCY", "Deficiencies, Vitamin B12", "cyanocobalamin deficiency", "deficiency; cyanocobalamin", "cyanocobalamin; deficiency", "of vitamin b 12 deficiency", "deficiency of vitamin b 12", "Deficiency of vitamin B>12<", "vitamin b12 deficiency disease", "Vitamin B12 deficiency disease", "b12 deficiency disease vitamin", "Cobalamin deficiency (disorder)", "vitamin B12 deficiency (diagnosis)", "Deficiency of vitamin B<sub>12</sub>"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitamin B12 deficiency", "shortest_name_length": 17}
{"curie": "MONDO:0012169", "names": ["POF3", "Pof3", "premature ovarian failure 3", "Premature Ovarian Failure 3", "PREMATURE OVARIAN FAILURE 3", "primary ovarian insufficiency 3", "premature ovarian failure type 3", "PREMATURE OVARIAN FAILURE 3 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "premature ovarian failure 3", "shortest_name_length": 4}
{"curie": "MONDO:0011714", "names": ["FPLD7", "LCCNS", "lipodystrophy, familial partial, type 7", "LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 7", "lipodystrophy, partial, with congenital cataracts and neurodegeneration", "PARTIAL LIPODYSTROPHY, CONGENITAL CATARACTS, AND NEURODEGENERATION SYNDROME", "partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome", "PARTIAL LIPODYSTROPHY, CONGENITAL CATARACTS, WITH OR WITHOUT NEURODEGENERATION SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C4082301", "names": ["Developmental Porencephaly", "Porencephaly, Developmental"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Developmental Porencephaly", "shortest_name_length": 26}
{"curie": "UMLS:C4763743", "names": ["BAP1-Mutant Clear Cell Renal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "BAP1-Mutant Clear Cell Renal Cell Carcinoma", "shortest_name_length": 43}
{"curie": "UMLS:C4525079", "names": ["Recurrent Langerhans Cell Histiocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Langerhans Cell Histiocytosis", "shortest_name_length": 39}
{"curie": "UMLS:C0161002", "names": ["corneal foreign body", "Corneal foreign body", "cornea; foreign body", "Corneal Foreign Body", "foreign body; cornea", "Foreign body in cornea", "Corneal foreign body (disorder)", "corneal foreign body (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Corneal foreign body (disorder)", "shortest_name_length": 20}
{"curie": "MONDO:0007681", "names": ["FMNG", "MNG1", "Familial MNG", "familial MNG", "SIMPLE GOITER", "simple goiter", "Simple goiter", "Euthyroid goitre", "euthyroid goiter", "EUTHYROID GOITER", "euthyroid goitre", "Euthyroid Goiter", "Euthyroid goiter", "GOITER, EUTHYROID", "Familial multinodular goiter", "multinodular goiter, adolescent", "MULTINODULAR GOITER, ADOLESCENT", "Multinodular goiter, adolescent", "Familial multinodular goiter syndrome", "Goiter, nontoxic, with intrathyroidal calcification", "goiter, nontoxic, with Intrathyroidal calcification", "GOITER, NONTOXIC, WITH INTRATHYROIDAL CALCIFICATION", "goiter, multinodular 1, with or without Sertoli-Leydig cell tumors", "GOITER, MULTINODULAR 1, WITH OR WITHOUT SERTOLI-LEYDIG CELL TUMORS", "Goiter, multinodular 1, with or without sertoli-leydig cell tumors"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "goiter, multinodular 1, with or without Sertoli-Leydig cell tumors", "shortest_name_length": 4}
{"curie": "UMLS:C4055496", "names": ["APL with t(17;17)(q21;q21); STAT5B-RARA", "Acute Myeloid Leukemia with t(17;17)(q21;q21)", "Acute Promyelocytic Leukemia with t(17;17)(q21;q21); STAT5B-RARA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Myeloid Leukemia with t(17;17)(q21;q21)", "shortest_name_length": 39}
{"curie": "MONDO:0020474", "names": ["Cheirospondyloenchondromatosis", "cheirospondyloenchondromatosis", "Cheirospondyloenchondromatosis (disorder)", "Generalised enchondromatosis with platyspondyly", "Generalized enchondromatosis with platyspondyly", "generalized enchondromatosis with platyspondyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cheirospondyloenchondromatosis", "shortest_name_length": 30}
{"curie": "MONDO:0001182", "names": ["idiopathic corneal edema", "Idiopathic corneal edema", "Idiopathic corneal oedema", "Idiopathic corneal edema (disorder)", "idiopathic corneal edema (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic corneal edema", "shortest_name_length": 24}
{"curie": "UMLS:C0751643", "names": ["Orbitofrontal epilepsy", "Orbito-Frontal Epilepsy", "Epilepsy, Orbito-Frontal", "Epilepsy, Orbito Frontal", "Orbito-Frontal Epilepsies", "Epilepsies, Orbito-Frontal", "Orbitofrontal epilepsy (disorder)", "Orbitofrontal epilepsy (diagnosis)", "frontal lobe epilepsy orbitofrontal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epilepsy, Orbito-Frontal", "shortest_name_length": 22}
{"curie": "MONDO:0016269", "names": ["high-grade neuroendocrine carcinoma of the corpus uteri", "high-grade neuroendocrine carcinoma of the uterine corpus", "poorly differentiated neuroendocrine carcinoma of the endometrium", "poorly differentiated neuroendocrine carcinoma of the corpus uteri"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "high-grade neuroendocrine carcinoma of the corpus uteri", "shortest_name_length": 55}
{"curie": "UMLS:C4331013", "names": ["Plasma Kallikrein Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Plasma Kallikrein Deficiency", "shortest_name_length": 28}
{"curie": "UMLS:C5237069", "names": ["Refractory Endometrial Undifferentiated Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Endometrial Undifferentiated Carcinoma", "shortest_name_length": 49}
{"curie": "MONDO:0005943", "names": ["Rhabditida Infection", "Rhabditida infection", "Rhabditida Infections", "Rhabditida infections", "Infection, Rhabditida", "infection, Rhabditida", "Infections, Rhabditida", "infections, Rhabditida", "Rhabditida infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rhabditida infectious disease", "shortest_name_length": 20}
{"curie": "UMLS:C1336077", "names": ["Sporadic Burkitt lymphoma", "Sporadic Burkitt Lymphoma", "Sporadic Burkitt's Lymphoma", "Sporadic Burkitt's lymphoma", "Non-endemic Burkitt's lymphoma", "Sporadic Burkitt's lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sporadic Burkitt's lymphoma", "shortest_name_length": 25}
{"curie": "MONDO:0018919", "names": ["MAS", "PFD", "POFD", "McCune-Albright", "ALBRIGHT DISEASE", "albright disease", "albright syndrome", "ALBRIGHT SYNDROME", "Albright Syndrome", "Albright syndrome", "Syndrome, Albright", "Albright's Disease", "albright's disease", "albrights syndrome", "Albright's disease", "Albright's syndrome", "ALBRIGHT'S SYNDROME", "albright's syndrome", "Albright's Syndrome", "Syndrome, Albright's", "albright's disease bone", "McCune Albright Syndrome", "mccune albright syndrome", "MCCUNE-ALBRIGHT SYNDROME", "McCune Albright syndrome", "McCune-Albright syndrome", "McCune-Albright Syndrome", "Albright's disease, bone", "mccune-albright syndrome", "fibrous dysplasia of bone", "Syndrome, McCune-Albright", "albrights mccune syndrome", "Albright's disease of bone", "Albright's Disease of Bone", "Albright-Sternberg Syndrome", "Albright-Sternberg syndrome", "polyostotic; fibrodysplasia", "fibrodysplasia; polyostotic", "osteitis fibrosa disseminata", "Osteitis fibrosa disseminata", "polyostotic fibrous dysplasia", "Polyostotic fibrous dysplasia", "POLYOSTOTIC FIBROUS DYSPLASIA", "Polyostotic Fibrous Dysplasia", "Fibrous Dysplasia, Polyostotic", "dysplasia; polyostotic fibrous", "Polyostotic Fibrous Dysplasias", "polyostotic fibrous; dysplasia", "osteitis; fibrosa, disseminata", "polyostotic; fibrous dysplasia", "Dysplasia, Polyostotic Fibrous", "MAS - McCune-Albright syndrome", "fibrosa; osteitis, disseminata", "Dysplasias, Polyostotic Fibrous", "Fibrous Dysplasias, Polyostotic", "fibrous; dysplasia, polyostotic", "Dysplasia, fibrous, polyostotic", "polyostotic; dysplasia, fibrous", "dysplasia; fibrous, polyostotic", "Albright-Mccune-Sternberg Syndrome", "Albright-McCune-Sternberg syndrome", "McCune Albright syndrome (disorder)", "PFD - Polyostotic fibrous dysplasia", "McCune-Albright syndrome (diagnosis)", "POFD - Polyostotic fibrous dysplasia", "Polyostotic fibrous dysplasia of bone", "Polyostotic Fibrous Dysplasia of Bone", "Albright(-McCune)(-Sternberg) syndrome", "albright(-McCune)(-Sternberg) syndrome", "polyostotic fibrous dysplasia (diagnosis)", "mccune-albright syndrome, somatic, mosaic", "Polyostotic fibrous dysplasia of bone, NOS", "Albright's Syndrome with Precocious Puberty", "Albright's syndrome with precocious puberty", "Polyostotic fibrous dysplasia of bone (disorder)", "gonadotropin-independent female-limited sexual precocity", "Gonadotropin-independent female-limited sexual precocity", "Fibrous Dysplasia with Pigmentary Skin Changes and Precocious Puberty", "Fibrous dysplasia with pigmentary skin changes and precocious puberty"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "McCune-Albright syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C1514423", "names": ["Primary Low Grade B-Cell Dural Lymphoma", "Primary Low-Grade B-Cell Lymphoma of Dura", "Primary Low-Grade B-Cell Lymphoma of the Dura"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Low Grade B-Cell Dural Lymphoma", "shortest_name_length": 39}
{"curie": "UMLS:C5420048", "names": ["Sinonasal Angiosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Angiosarcoma", "shortest_name_length": 22}
{"curie": "UMLS:C0854761", "names": ["Recurrent Esophagus Cancer", "Relapsed Esophageal Cancer", "esophagus cancer, recurrent", "Recurrent Esophageal Cancer", "recurrent esophageal cancer", "ESOPHAGEAL CANCER RECURRENT", "esophageal cancer, recurrent", "Relapsed Cancer of Esophagus", "Relapsed Esophagus Carcinoma", "Recurrent Cancer of Esophagus", "Esophageal carcinoma recurrent", "Recurrent Esophageal Carcinoma", "Oesophageal carcinoma recurrent", "Oesophageal Carcinoma Recurrent", "Relapsed Carcinoma of Esophagus", "Esophageal Carcinoma, Recurrent", "Relapsed Cancer of the Esophagus", "Recurrent Carcinoma of Esophagus", "Recurrent Cancer of the Esophagus", "Relapsed Carcinoma of the Esophagus", "Recurrent Carcinoma of the Esophagus", "Esophageal carcinoma site unspecified recurrent", "Oesophageal carcinoma site unspecified recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal carcinoma recurrent", "shortest_name_length": 26}
{"curie": "MONDO:0019548", "names": ["CMTDI", "autosomal dominant intermediate Charcot-Marie-Tooth", "autosomal dominant intermediate Charcot-Marie-Tooth disease", "intermediate Charcot-Marie-Tooth disease, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant intermediate Charcot-Marie-Tooth disease", "shortest_name_length": 5}
{"curie": "MONDO:0015453", "names": ["cogan syndrome", "Cogan syndrome", "Cogan Syndrome", "Syndrome, Cogan", "Cogans Syndrome", "cogans syndrome", "Cogan's syndrome", "Syndrome, Cogans", "Cogan's Syndrome", "cogan's syndrome", "Syndrome, Cogan's", "Oculomotor apraxia", "oculomotor apraxia", "apraxia oculomotor", "Cogan's syndrome (disorder)", "Cogan's syndrome (diagnosis)", "diffuse interstitual keratitis", "Oculovestibuloauditory syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cogan syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0007107", "names": ["anal sphincter myopathy, internal", "Anal Sphincter Myopathy, Internal", "ANAL SPHINCTER MYOPATHY, INTERNAL", "PROCTALGIA FUGAX DUE TO ANAL SPHINCTER MYOPATHY", "proctalgia fugax due to anal sphincter myopathy", "Proctalgia Fugax due to Anal Sphincter Myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anal sphincter myopathy, internal", "shortest_name_length": 33}
{"curie": "MONDO:0044700", "names": ["SIN3A-related intellectual disability syndrome due to a point mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SIN3A-related intellectual disability syndrome due to a point mutation", "shortest_name_length": 70}
{"curie": "UMLS:C0796611", "names": ["Ependymoma", "Newly Diagnosed Childhood Ependymoma", "newly diagnosed childhood ependymoma", "ependymoma, newly diagnosed childhood", "childhood ependymoma, newly diagnosed", "ependymoma, childhood, newly diagnosed"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Newly Diagnosed Childhood Ependymoma", "shortest_name_length": 10}
{"curie": "MONDO:0007277", "names": ["Wellesley Carman French syndrome", "Wellesley-Carman-French syndrome", "Wellesley Carmen French syndrome", "Cataract-aberrant oral frenula-growth delay syndrome", "cataract-aberrant oral frenula-growth delay syndrome", "CATARACT, ABERRANT ORAL FRENULA, AND GROWTH RETARDATION", "Cataract, Aberrant Oral Frenula, And Growth Retardation", "cataract, aberrant oral frenula, and growth retardation", "Cataracts, aberrant oral frenula, and growth retardation", "cataracts, aberrant oral frenula, and growth retardation", "Cataract with aberrant oral frenula and growth delay syndrome", "Cataract with aberrant oral frenula and growth delay syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract-aberrant oral frenula-growth delay syndrome", "shortest_name_length": 32}
{"curie": "UMLS:C5238241", "names": ["Unresectable Ovarian Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Ovarian Carcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0015042", "names": ["primary plasmacytoma of the bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary plasmacytoma of the bone", "shortest_name_length": 32}
{"curie": "MONDO:0009980", "names": ["Frenkel Russe syndrome", "retinal telangiectasia and hypogammaglobulinemia", "RETINAL TELANGIECTASIA AND HYPOGAMMAGLOBULINEMIA", "Retinal Telangiectasia and Hypogammaglobulinemia", "retinal telangiectasia associated with hypogammaglobulinemia", "Retinal telangiectasia associated with hypogammaglobulinemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal telangiectasia and hypogammaglobulinemia", "shortest_name_length": 22}
{"curie": "MONDO:0017018", "names": ["Isolated pulmonary capillaritis", "isolated pulmonary capillaritis", "Isolated pulmonary capillaritis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated pulmonary capillaritis", "shortest_name_length": 31}
{"curie": "UMLS:C2984902", "names": ["Malignant Intraocular Peripheral Nerve Sheath Tumor", "Intraocular Malignant Peripheral Nerve Sheath Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraocular Malignant Peripheral Nerve Sheath Tumor", "shortest_name_length": 51}
{"curie": "UMLS:C1970095", "names": ["Cleft Palate, Isolated, And Mental Retardation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cleft Palate, Isolated, And Mental Retardation", "shortest_name_length": 46}
{"curie": "UMLS:C1335006", "names": ["Non-Neoplastic Ear Disease", "Non-Neoplastic Ear Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Ear Disorder", "shortest_name_length": 26}
{"curie": "UMLS:C1720144", "names": ["Herpes zoster associated with AIDS", "Herpes zoster associated with AIDS (diagnosis)", "Herpes zoster with acquired immunodeficiency syndrome", "Herpes zoster with AIDS (acquired immunodeficiency syndrome)", "Herpes zoster with acquired immunodeficiency syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Herpes zoster with AIDS (acquired immunodeficiency syndrome)", "shortest_name_length": 34}
{"curie": "MONDO:0004750", "names": ["Language Disorder", "language handicap", "Language disorder", "language disorder", "disorder language", "language disorders", "Language Disorders", "disorders language", "Language disorders", "language disability", "language impairment", "impairment language", "disability language", "Language impairment", "Disorder of language", "impairments language", "Language disabilities", "disabilities language", "Language disorder NOS", "Disorder of language, NOS", "Disorder of language (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "language disorder", "shortest_name_length": 17}
{"curie": "UMLS:C0861624", "names": ["Stage IV Mouth Epidermoid Carcinoma", "Stage IV Mouth Squamous Cell Carcinoma", "Stage IV Epidermoid Carcinoma of Mouth", "Stage IV Oral Cavity Epidermoid Carcinoma", "Stage IV Squamous Cell Carcinoma of Mouth", "Stage IV Oral Cavity Squamous Cell Cancer", "Stage IV Epidermoid Carcinoma of the Mouth", "Stage IV Epidermoid Carcinoma of Oral Cavity", "Stage IV Oral Cavity Squamous Cell Carcinoma", "Stage IV Squamous Cell Carcinoma of the Mouth", "Stage IV Squamous Cell Carcinoma of Oral Cavity", "Stage IV Epidermoid Carcinoma of the Oral Cavity", "Squamous cell carcinoma of the oral cavity stage IV", "Stage IV Squamous Cell Carcinoma of the Oral Cavity", "Stage IV Oral Cavity Squamous Cell Carcinoma AJCC v7", "Stage IV Oral Cavity Squamous Cell Carcinoma AJCC v6", "Stage IV Oral Cavity Squamous Cell Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Squamous cell carcinoma of the oral cavity stage IV", "shortest_name_length": 35}
{"curie": "MONDO:0019270", "names": ["erythrokeratoderma", "Erythrokeratoderma", "Erythrokeratoderma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythrokeratoderma", "shortest_name_length": 18}
{"curie": "UMLS:C0347203", "names": ["Benign Palate Tumor", "Benign Palate Neoplasm", "Benign tumor of palate", "Benign Tumor of Palate", "Benign tumour of palate", "Benign neoplasm of palate", "benign neoplasm of palate", "Benign Neoplasm of Palate", "Benign Tumor of the Palate", "Benign Neoplasm of the Palate", "Benign tumor of roof of mouth", "Benign neoplasm of the palate", "Benign neoplasm of palate, NOS", "Benign tumour of roof of mouth", "Benign neoplasm of palate (disorder)", "benign neoplasm of palate (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign neoplasm of palate", "shortest_name_length": 19}
{"curie": "UMLS:C4330492", "names": ["Insulin Receptor Mutation - Associated Insulin Resistance Syndromes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Insulin Receptor Mutation - Associated Insulin Resistance Syndromes", "shortest_name_length": 67}
{"curie": "UMLS:C0151538", "names": ["Buccoglossal syndrome", "Syndrome buccoglossal", "SYNDROME BUCCOGLOSSAL", "BUCCOGLOSSAL SYNDROME", "DYSKINESIA BUCCOGLOSSAL", "Dyskinesia buccoglossal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Buccoglossal syndrome", "shortest_name_length": 21}
{"curie": "MONDO:0001098", "names": ["Separation anxiety", "anxiety separation", "separation anxiety", "Separation Anxiety", "anxiety separations", "Anxiety, Separation", "Separation anxiety disorder", "separation anxiety disorder", "anxiety disorder separation", "Separation Anxiety Disorder", "anxiety separation disorder", "childhood separation anxiety", "separation anxiety; disorder", "Anxiety Disorder, Separation", "disorder; separation anxiety", "Separation anxiety (disorder)", "Separation anxiety, childhood", "separation anxiety (diagnosis)", "Separation anxiety in children", "Separation anxiety disorder of childhood", "separation anxiety disorder of childhood", "Separation anxiety disorder of childhood (disorder)", "separation anxiety disorder of childhood (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "separation anxiety disorder", "shortest_name_length": 18}
{"curie": "UMLS:C1336336", "names": ["Esophageal Cancer Stage IVA", "Stage IVA Esophageal Cancer", "Stage IVA Esophagus Carcinoma", "Stage IVA Esophageal Carcinoma", "Stage IVA Carcinoma of Esophagus", "Stage IVA Carcinoma of the Esophagus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Esophageal Carcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0030519", "names": ["AGM9", "agammaglobulinemia 9", "agammaglobulinemia 9, autosomal recessive", "AGAMMAGLOBULINEMIA 9, AUTOSOMAL RECESSIVE", "AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO SLC39A7 DEFECT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "agammaglobulinemia 9, autosomal recessive", "shortest_name_length": 4}
{"curie": "MONDO:0006408", "names": ["Sex Hormone-Producing Adrenal Gland Adenoma", "Sex Hormone-Producing Adrenal Cortex Adenoma", "Sex hormone producing adrenal cortex adenoma", "Sex Hormone Producing Adrenal Cortex Adenoma", "sex hormone-producing adrenal cortex adenoma", "Sex Hormone-Producing Adrenal Cortical Adenoma", "Sex Hormone Producing Adrenal Cortical Adenoma", "Sex hormone producing adrenal cortical adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sex hormone-producing adrenal cortex adenoma", "shortest_name_length": 43}
{"curie": "MONDO:0002643", "names": ["VESTIBULAR PROBLEM", "Vestibular disease", "Vestibular Disease", "vestibular problem", "vestibular disease", "disorder vestibular", "Disorder vestibular", "Disease, Vestibular", "Vestibular Diseases", "vestibular diseases", "problems vestibular", "Vestibular syndrome", "DISORDER VESTIBULAR", "VESTIBULAR DISORDER", "vestibular disorder", "Vestibular disorder", "Diseases, Vestibular", "disorders vestibular", "Vestibular disorder NOS", "Vestibular disorder, NOS", "vestibular system disease", "vestibular system disorder", "Disorder;vestibular system", "disorders system vestibular", "vestibular labyrinth disease", "vertigo, vestibular disorder", "Vertigo, vestibular disorder", "disease of vestibular system", "Vestibular function disorder", "disorder; vestibular function", "vestibular function; disorder", "Vestibular disease (disorder)", "disorder of vestibular system", "Vestibular disease or syndrome", "disease of vestibular labyrinth", "disorder of vestibular function", "disorder of vestibular labyrinth", "Disorders of vestibular function", "disease (or disorder); labyrinth, ear", "vestibular labyrinth disease or disorder", "disease or disorder of vestibular labyrinth", "disorder of vestibular function (diagnosis)", "Unspecified disorder of vestibular function", "Disorder of vestibular function, unspecified", "Unspecified disorder of vestibular function, unspecified ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vestibular disorder", "shortest_name_length": 18}
{"curie": "MONDO:0013329", "names": ["CHROMOSOME 17q23.1-q23.2 DUPLICATION SYNDROME", "chromosome 17q23.1-q23.2 DUPLICATION syndrome", "familial clubfoot due to 17q23.1q23.2 microduplication", "Familial clubfoot due to 17q23.1q23.2 microduplication", "Hereditary clubfoot due to 17q23.1-q23.2 microduplication", "hereditary clubfoot due to 17q23.1-q23.2 microduplication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial clubfoot due to 17q23.1q23.2 microduplication", "shortest_name_length": 45}
{"curie": "UMLS:C0152972", "names": ["Pseudomonal sepsis", "pseudomonas sepsis", "PSEUDOMONAS SEPSIS", "Septicemia pseudomonal", "pseudomonas septicemia", "Pseudomonas septicemia", "Septicaemia pseudomonal", "Pseudomonas septicaemia", "Septicemia due to pseudomonas", "Septicemia due to Pseudomonas", "Septicaemia due to pseudomonas", "Septicaemia due to Pseudomonas", "Pseudomonas septicemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pseudomonal sepsis", "shortest_name_length": 18}
{"curie": "MONDO:0005800", "names": ["STY", "Sty", "sty", "STYE", "stye", "Stye", "styes", "Styes", "Hordeola", "HORDEOLUM", "hordeolum", "Hordeolum", "Hordeolas", "Hordeolum NOS", "Stye of eyelid", "Boil of eyelid", "Hordeolum, NOS", "boil of eyelid", "Red bump on eyelid", "Hordeolum externum", "Furuncle of eyelid", "furuncle of eyelid", "Hordeolum (disorder)", "eyelid gland blepharitis", "blepharitis of eyelid gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hordeolum", "shortest_name_length": 3}
{"curie": "MONDO:0007068", "names": ["ADSLD", "ADSL Deficiency", "Adsl deficiency", "ADSL DEFICIENCY", "ADSL deficiency", "Succinyladenosinuria", "Succinylpurinemic autism", "Succinylpurinaemic autism", "Adenylosuccinase deficiency", "Adenylosuccinate deficiency", "ADENYLOSUCCINASE DEFICIENCY", "adenylosuccinase deficiency", "ADENYLOSUCCINATE LYASE DEFICIENCY", "Adenylosuccinate lyase deficiency", "adenylosuccinate lyase deficiency", "adenylosuccinase lyase deficiency", "Deficiency of adenylosuccinate lyase", "ASase - Adenylosuccinate lyase deficiency", "Adenylosuccinate lyase deficiency (disorder)", "inborn error of (S)-2-(5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxamido)succinate AMP-lyase (fumarate-forming) activity", "inborn (S)-2-(5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxamido)succinate AMP-lyase (fumarate-forming) activity disorder", "rare inborn error of (S)-2-(5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxamido)succinate AMP-lyase (fumarate-forming) activity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenylosuccinate lyase deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0018603", "names": ["interstitial lung disease due to SP-C deficiency", "interstitial lung disease due to surfactant protein C deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "interstitial lung disease due to SP-C deficiency", "shortest_name_length": 48}
{"curie": "UMLS:C0013922", "names": ["Embolic", "embolism", "EMBOLISM", "Embolism", "Embolisms", "Embolism NOS", "Embolism, NOS", "Embolism/Embolus", "Embolism (disorder)", "embolism (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Embolism", "shortest_name_length": 7}
{"curie": "UMLS:C5206897", "names": ["Localized Childhood Rhabdomyosarcoma", "Non-Metastatic Childhood Rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized Childhood Rhabdomyosarcoma", "shortest_name_length": 36}
{"curie": "UMLS:C5239595", "names": ["Myelodysplastic Syndrome, Unclassifiable, with Single Lineage Dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myelodysplastic Syndrome, Unclassifiable, with Single Lineage Dysplasia", "shortest_name_length": 71}
{"curie": "UMLS:C0751460", "names": ["Flaccid tetraplegia", "Flaccid Tetraplegia", "tetraplegia; flaccid", "Tetraplegia, Flaccid", "Flaccid Quadriplegia", "flaccid quadriplegia", "Flaccid quadriplegia", "quadriplegia flaccid", "flaccid; tetraplegia", "Flaccid Tetraplegias", "Flaccid Quadriplegias", "Tetraplegias, Flaccid", "quadriplegia; flaccid", "flaccid; quadriplegia", "Quadriplegia, Flaccid", "Quadriplegias, Flaccid", "Flaccid tetraplegia (disorder)", "flaccid quadriplegia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Flaccid Quadriplegia", "shortest_name_length": 19}
{"curie": "UMLS:C0744235", "names": ["Fungal sepsis", "FUNGAL SEPSIS", "fungal sepsis", "Mycotic sepsis", "Sepsis due to fungus", "Sepsis caused by fungus", "Sepsis caused by fungus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sepsis due to fungus", "shortest_name_length": 13}
{"curie": "MONDO:0019109", "names": ["CANDA syndrome", "CANOMAD syndrome", "chronic sensory ataxic neuropathy with anti-disialosyl antibodies", "chronic sensory ataxic neuropathy with anti-dyalosyl IgM antibodies", "Chronic sensory ataxic neuropathy with anti-dyalosyl IgM antibodies", "Chronic sensory ataxic neuropathy with anti-disialosyl IgM antibodies", "chronic ataxic neuropathy ophthalmoplegia M-protein agglutination disialosyl antibodies syndrome", "chronic ataxic neuropathy-ophthalmoplegia-IgM paraprotein-cold agglutinins-disialosyl antibodies syndrome", "Chronic ataxic neuropathy-ophthalmoplegia-IgM paraprotein-cold agglutinins-disialosyl antibodies syndrome", "Chronic ataxic neuropathy, ophthalmoplegia, monoclonal IgM protein, cold agglutinins and disialosyl antibodies", "CANOMAD (chronic ataxic neuropathy, ophthalmoplegia, monoclonal IgM protein, cold agglutinins and disialosyl antibodies) syndrome", "Chronic ataxic neuropathy, ophthalmoplegia, monoclonal immunoglobulin M protein, cold agglutinin and disialosyl antibody syndrome", "Chronic ataxic neuropathy, ophthalmoplegia, monoclonal immunoglobulin M protein, cold agglutinin and disialosyl antibody syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CANOMAD syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0001790", "names": ["Spinal cord lipoma", "Spinal Cord Lipoma", "spinal cord lipoma", "Lipoma of spinal cord", "Lipoma of Spinal Cord", "lipoma of spinal cord", "Lipoma of spinal cord (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal cord lipoma", "shortest_name_length": 18}
{"curie": "UMLS:C0028047", "names": ["Nicotine Withdrawal", "withdrawal nicotine", "Nicotine withdrawal", "nicotine withdrawal", "nicotine withdrawals", "Nicotine withdrawal syndrome", "nicotine withdrawal (diagnosis)", "Nicotine withdrawal syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nicotine withdrawal", "shortest_name_length": 19}
{"curie": "MONDO:0011871", "names": ["NPD-B", "ASMD, VISCERAL TYPE", "Chronic visceral ASMD", "Niemann Pick disease type B", "type B Niemann-Pick disease", "Type B Niemann-Pick Disease", "Type B Niemann Pick Disease", "Niemann-Pick disease type B", "Niemann-Pick disease, type F", "Niemann-Pick Disease, Type B", "Niemann-Pick disease, type B", "Niemann Pick Disease, Type B", "Niemann-Pick disease, type E", "Niemann-Pick Disease, Type F", "Niemann Pick Disease, Type E", "Niemann-PICK disease, type B", "NIEMANN-PICK DISEASE, TYPE E", "Niemann-Pick Disease, Type E", "NIEMANN-PICK DISEASE, TYPE F", "NIEMANN-PICK DISEASE, TYPE B", "Niemann Pick's Disease Type E", "Niemann-Pick's Disease Type B", "Niemann-Pick's Disease Type E", "Niemann Pick's Disease Type B", "Niemann-Pick Disease, Visceral", "Niemann Pick Disease, Visceral", "Niemann-Pick disease type B (diagnosis)", "Niemann-Pick disease, type B (disorder)", "Niemann-Pick disease non-neuropathic type", "Niemann-Pick Disease, Non-Neuronopathic Type", "Niemann Pick Disease, Non Neuronopathic Type", "Niemann-Pick disease, adult non-neuronopathic", "Niemann Pick Disease, Adult Non Neuronopathic", "Niemann-Pick Disease, Adult Non-Neuronopathic", "ACID SPHINGOMYELINASE DEFICIENCY, VISCERAL TYPE", "Niemann-Pick disease, chronic non-neuronopathic", "Chronic visceral acid sphingomyelinase deficiency", "Niemann-Pick disease, Intermediate, with visceral involvement and rapid progression", "Niemann-Pick Disease, Intermediate, With Visceral Involvement And Rapid Progression", "NIEMANN-PICK DISEASE, INTERMEDIATE, WITH VISCERAL INVOLVEMENT AND RAPID PROGRESSION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Niemann-Pick disease type B", "shortest_name_length": 5}
{"curie": "MONDO:0001642", "names": ["stye", "Stye", "Hordeolum", "Eyelid boil", "sty external", "external stye", "STY, EXTERNAL", "Boil of eyelid", "eyelid; furuncle", "furuncle; eyelid", "externum hordeolum", "hordeolum externum", "hordeolum external", "Hordeolum externum", "Furuncle of eyelid", "External hordeolum", "external hordeolum", "HORDEOLUM, EXTERNAL", "Hordeolum, external", "furuncles on eyelid", "Hordeolum externum (disorder)", "hordeolum externum (diagnosis)", "furuncles on eyelid (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hordeolum externum", "shortest_name_length": 4}
{"curie": "UMLS:C0855039", "names": ["Metastatic Epithelioid Sarcoma", "Epithelioid sarcoma metastatic", "Epithelioid Sarcoma, Metastatic", "Metastatic Epithelioid Cell Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epithelioid sarcoma metastatic", "shortest_name_length": 30}
{"curie": "UMLS:C5205934", "names": ["Prostate Cystadenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Cystadenoma", "shortest_name_length": 20}
{"curie": "UMLS:C0030330", "names": ["Peritoneal Panniculitis", "Panniculitis, Peritoneal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Panniculitis, Peritoneal", "shortest_name_length": 23}
{"curie": "MONDO:0008095", "names": ["Nevus Anemicus", "NEVUS anemicus", "anemicus Nevus", "Anemicus Nevus", "nevus anemicus", "Nevus anemicus", "NEVUS ANEMICUS", "Naevus anemicus", "Nevus oligemicus", "Naevus anaemicus", "Nevus oligaemicus", "Naevus oligaemicus", "nevus anemicus (disease)", "Nevus anemicus (disorder)", "Nevus anemicus et oligemicus", "Nevus anemicus et oligaemicus", "Naevus anaemicus et oligaemicus", "anomalies of skin nevus anemicus", "anomalies of skin nevus anemicus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nevus anemicus", "shortest_name_length": 14}
{"curie": "MONDO:0018742", "names": ["familial type 1 gNET", "hereditary type 1 gNET", "familial gastric type 1 neuroendocrine tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial gastric type 1 neuroendocrine tumor", "shortest_name_length": 20}
{"curie": "MONDO:0100160", "names": ["alcoholic ketosis", "alcoholic acidosis", "alcoholic ketoacidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alcoholic ketoacidosis", "shortest_name_length": 17}
{"curie": "MONDO:0019236", "names": ["disorder of purine metabolism", "inborn disorder of purine metabolism", "inborn purine nucleobase metabolic process disorder", "inborn error of purine nucleobase metabolic process", "rare inborn error of purine nucleobase metabolic process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of purine metabolism", "shortest_name_length": 29}
{"curie": "MONDO:0008510", "names": ["Learman syndrome", "Symphalangism with Multiple Anomalies of Hands and Feet", "Symphalangism with multiple anomalies of hands and feet", "symphalangism with multiple anomalies of hands and feet", "SYMPHALANGISM WITH MULTIPLE ANOMALIES OF HANDS AND FEET", "Symphalangism with multiple anomalies of hands and feet syndrome", "Symphalangism with multiple anomalies of hands and feet syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "symphalangism with multiple anomalies of hands and feet", "shortest_name_length": 16}
{"curie": "MONDO:0010851", "names": ["Lowry-MacLean syndrome", "LOWRY-MACLEAN SYNDROME", "Lowry Maclean syndrome", "Lowry MacLean syndrome", "Lowry-Maclean Syndrome", "Lowry MacLean syndrome (disorder)", "Lowry MacLean syndrome (diagnosis)", "mental retardation, cleft palate, eventration of diaphragm, congenital heart defect, glaucoma, craniosynostosis and growth failure", "Mental retardation, cleft palate, eventration of diaphragm, congenital heart defect, glaucoma, craniosynostosis, and growth failure", "intellectual disability, cleft palate, eventration of diaphragm, congenital heart defect, glaucoma, craniosynostosis and growth failure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lowry-MacLean syndrome", "shortest_name_length": 22}
{"curie": "UMLS:C1377599", "names": ["Childhood CNS Teratoma", "Pediatric CNS Teratoma", "childhood CNS teratoma", "Childhood Teratoma of CNS", "Pediatric Teratoma of CNS", "Childhood Teratoma of the CNS", "Pediatric Teratoma of the CNS", "Central Nervous System Teratoma", "Childhood Central Nervous System Teratoma", "childhood central nervous system teratoma", "Pediatric Central Nervous System Teratoma", "Childhood Teratoma of Central Nervous System", "Pediatric Teratoma of Central Nervous System", "Childhood Teratoma of the Central Nervous System", "Pediatric Teratoma of the Central Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Central Nervous System Teratoma", "shortest_name_length": 22}
{"curie": "UMLS:C4521803", "names": ["Stage III Anal Cancer", "Stage III Anal Cancer AJCC v8", "Stage III Anal Carcinoma AJCC v8", "Stage III Anal Canal and Perianal (Anal Margin) Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Anal Cancer AJCC v8", "shortest_name_length": 21}
{"curie": "UMLS:C4329365", "names": ["Atypical PitNET/Adenoma", "Atypical Pituitary Gland Adenoma", "Atypical Pituitary Neuroendocrine Tumor", "Atypical Pituitary Neuroendocrine Tumor/Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypical Pituitary Neuroendocrine Tumor", "shortest_name_length": 23}
{"curie": "UMLS:C4526978", "names": ["Stage III Small Intestinal, Esophageal, Colorectal, Mesenteric, and Peritoneal GIST AJCC v8", "Stage III Small Intestinal, Esophageal, Colorectal, Mesenteric, and Peritoneal Gastrointestinal Stromal Tumor (GIST)", "Stage III Small Intestinal, Esophageal, Colorectal, Mesenteric, and Peritoneal Gastrointestinal Stromal Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Small Intestinal, Esophageal, Colorectal, Mesenteric, and Peritoneal Gastrointestinal Stromal Tumor AJCC v8", "shortest_name_length": 91}
{"curie": "UMLS:C1336119", "names": ["Stage IA Non-Small Cell Lung Cancer", "stage IA non-small cell lung cancer", "Stage IA Non-Oat Cell Lung Carcinoma", "Stage IA Non-Small Cell Lung Carcinoma", "stage IA non-small cell lung carcinoma", "Stage IA Non-Oat Cell Carcinoma of Lung", "Stage IA Non-Small Cell Carcinoma of Lung", "stage IA non-small cell carcinoma of lung", "Stage IA Non-Oat Cell Carcinoma of the Lung", "Stage IA Non-Small Cell Carcinoma of the Lung", "stage IA non-small cell carcinoma of the lung", "Stage IA Non-Small Cell Lung Carcinoma AJCC v7", "Stage IA Lung Non-Small Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Lung Non-Small Cell Carcinoma AJCC v7", "shortest_name_length": 35}
{"curie": "UMLS:C5420384", "names": ["Fibrinolysis Shutdown"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fibrinolysis Shutdown", "shortest_name_length": 21}
{"curie": "UMLS:C2981673", "names": ["Stage IIB Ampulla of Vater Cancer", "Stage IIB Ampulla of Vater Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Ampulla of Vater Cancer AJCC v7", "shortest_name_length": 33}
{"curie": "MONDO:0006992", "names": ["AORTITIS SYPHILITIC", "Syphilitic Aortitis", "syphilitic aortitis", "Aortitis syphilitic", "aortitis syphilitic", "Syphilitic aortitis", "AORTITIS, SYPHILITIC", "Aortitis, Syphilitic", "Aortitis, syphilitic", "Syphilitic Aortitides", "DOEHLE-HELLER AORTITIS", "Aortitides, Syphilitic", "Doehle-Heller (etiology)", "CV syphilis of aortic artery", "Doehle-Heller (manifestation)", "Syphilitic aortitis (disorder)", "syphilitic aortitis (diagnosis)", "aortitis; Doehle-Heller (etiology)", "Doehle-Heller; aortitis (etiology)", "Late quaternary syphilitic aortitis", "Doehle-Heller; aortitis (manifestation)", "aortitis; Doehle-Heller (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syphilitic aortitis", "shortest_name_length": 19}
{"curie": "UMLS:C0750977", "names": ["Recurrent Brain Tumor", "recurrent brain tumors", "Recurrent Brain Tumors", "Brain Tumor, Recurrent", "brain tumors recurrent", "Brain Tumors, Recurrent", "Recurrent Brain Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Brain Neoplasm", "shortest_name_length": 21}
{"curie": "UMLS:C2987166", "names": ["Medullary carcinoma", "Pancreatic Medullary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Medullary Carcinoma", "shortest_name_length": 19}
{"curie": "UMLS:C2586050", "names": ["ulcerative esophagitis", "Esophagitis ulcerative", "Ulcerative esophagitis", "Oesophagitis ulcerative", "Ulcerative oesophagitis", "ulcerative oesophagitis", "peptic ulcer of esophagus", "Ulcerative esophagitis (disorder)", "ulcerative esophagitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ulcerative esophagitis", "shortest_name_length": 22}
{"curie": "MONDO:0007214", "names": ["CHRISTIAN BRACHYDACTYLY", "Christian brachydactyly", "Christian Brachydactyly", "brachydactyly-preaxial hallux varus syndrome", "preaxial brachydactyly with hallux varus and thumb abduction", "brachydactyly preaxial with hallux varus and thumb abduction", "Brachydactyly preaxial with hallux varus and thumb abduction", "BRACHYDACTYLY, PREAXIAL, WITH HALLUX VARUS AND THUMB ABDUCTION", "Brachydactyly, Preaxial, With Hallux Varus And Thumb Abduction", "brachydactyly, preaxial, with hallux varus and thumb abduction", "dominant preaxial brachydactyly with hallux varus and thumb abduction", "Dominant preaxial brachydactyly with hallux varus and thumb abduction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly-preaxial hallux varus syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0045063", "names": ["major salivary gland adenoid cystic cancer", "Major Salivary Gland Adenoid Cystic Cancer", "Major Salivary Gland Adenoid Cystic Carcinoma", "major salivary gland adenoid cystic carcinoma", "adenoid cystic carcinoma of major salivary gland", "Adenoid Cystic Carcinoma of Major Salivary Gland", "Adenoid Cystic Carcinoma of the Major Salivary Gland", "adenoid cystic carcinoma of the major salivary gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "major salivary gland adenoid cystic carcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0008141", "names": ["familial ossicular malformations", "Familial ossicular malformations", "Ossicular Malformations, familial", "ossicular malformations, familial", "OSSICULAR MALFORMATIONS, FAMILIAL", "familial middle ear ossicular anomalies", "Familial middle ear ossicular anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ossicular malformations, familial", "shortest_name_length": 32}
{"curie": "MONDO:0007616", "names": ["FIBULA, RECURRENT DISLOCATION OF HEAD OF", "fibula, recurrent dislocation of head of", "Fibula, Recurrent Dislocation of Head of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibula, recurrent dislocation of head of", "shortest_name_length": 40}
{"curie": "UMLS:C4528637", "names": ["Stage I Lentigo Maligna AJCC v7", "Stage I Lentigo Maligna Melanoma", "Stage I Lentigo Maligna Melanoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Lentigo Maligna Melanoma AJCC v7", "shortest_name_length": 31}
{"curie": "MONDO:0016477", "names": ["Beckwith-Wiedemann syndrome due to 11p15 microdeletion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Beckwith-Wiedemann syndrome due to 11p15 microdeletion", "shortest_name_length": 54}
{"curie": "MONDO:0007857", "names": ["palmoplantar keratoderma-clinodactyly syndrome", "Keratosis Palmaris et Plantaris with Clinodactyly", "keratosis palmaris ET plantaris with clinodactyly", "KERATOSIS PALMARIS ET PLANTARIS WITH CLINODACTYLY", "keratosis palmaris et plantaris-clinodactyly syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratosis palmaris et plantaris-clinodactyly syndrome", "shortest_name_length": 46}
{"curie": "MONDO:0032618", "names": ["MC1DN13", "nuclear type mitochondrial complex I deficiency 13", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 13", "mitochondrial complex 1 deficiency, nuclear type 13"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 13", "shortest_name_length": 7}
{"curie": "UMLS:C0279916", "names": ["stage III childhood HD", "childhood HD, stage III", "pediatric HD, stage III", "HD, stage III, childhood", "HD, childhood, stage III", "Stage III Hodgkin Lymphoma", "Stage III Childhood Hodgkin Lymphoma", "stage III childhood Hodgkin lymphoma", "stage III pediatric Hodgkin's disease", "Childhood Hodgkin's Disease Stage III", "Pediatric Hodgkin's Disease Stage III", "stage III childhood Hodgkin's disease", "stage III Hodgkin's disease, childhood", "Pediatric Hodgkin's Lymphoma Stage III", "Stage III Pediatric Hodgkin's Lymphoma", "Childhood Hodgkin's Lymphoma Stage III", "Stage III Childhood Hodgkin's Lymphoma", "pediatric Hodgkin's disease, stage III", "childhood Hodgkin's lymphoma, stage III", "Hodgkin's disease, stage III, childhood", "lymphoma, stage III childhood Hodgkin's", "Hodgkin's lymphoma, stage III, childhood", "Ann Arbor Stage III Childhood Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Childhood Hodgkin Lymphoma", "shortest_name_length": 22}
{"curie": "MONDO:0015183", "names": ["Short-gut syndrome", "Short gut syndrome", "SHORT GUT SYNDROME", "short gut syndrome", "SHORT-BOWEL SYNDROME", "Short-bowel syndrome", "short bowel syndrome", "Short Bowel Syndrome", "bowel short syndrome", "short-bowel syndrome", "Short bowel syndrome", "short bowel syndromes", "Bowel Syndrome, Short", "Syndrome, Short Bowel", "Short Bowel Syndromes", "Bowel Syndromes, Short", "Syndromes, Short Bowel", "SGS - Short gut syndrome", "syndrome intestine short", "Short intestine syndrome", "BOWEL SHORT BOWEL SYNDROME", "SBS - Short bowel syndrome", "Post-resection malabsorption", "short bowel syndrome acquired", "acquired short bowel syndrome", "Acquired short bowel syndrome", "Short bowel syndrome (disorder)", "MASSIVE BOWEL RESECTION SYNDROME", "short bowel syndrome (diagnosis)", "Post-resection short bowel syndrome", "Postresectional malabsorption syndrome", "Acquired short bowel syndrome (disorder)", "Acquired short bowel syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short bowel syndrome", "shortest_name_length": 18}
{"curie": "MONDO:0017376", "names": ["PIRA", "Reiter", "triad; Reiter", "Reiter; triad", "Reiter Disease", "reiter disease", "Reiter disease", "Reiters Disease", "reiter syndrome", "REITER SYNDROME", "Reiters disease", "disease reiters", "REITERS DISEASE", "Reiter syndrome", "syndrome reiter", "Reiter Syndrome", "reiters disease", "reiter's disease", "Reiter's disease", "reiters syndrome", "REITER'S DISEASE", "REITERS SYNDROME", "Reiters syndrome", "Reiters Syndrome", "Reiter's Disease", "reiter's syndrome", "Reiter's Syndrome", "REITER'S SYNDROME", "syndrome reiter's", "Reiter's syndrome", "Reactive arthritis", "Arthritis reactive", "venereal arthritis", "Venereal arthritis", "Reactive Arthritis", "reactive arthritis", "Arthritis, Reactive", "Reactive Arthritides", "Arthritis urethritica", "ARTHRITIS URETHRITICA", "arthritis urethritica", "Polyarthritis enterica", "polyarthritis enterica", "arthropathy; dysentery", "dysentery; arthropathy", "arthritis; urethritica", "urethritica; arthritis", "INFECTIOUS UROARTHRITIS", "Reactive arthritis triad", "uroarthritis; infectious", "Postinfectious Arthritis", "Post-infective arthritis", "Fiessinger-Leroy disease", "arthritis; postdysenteric", "postdysenteric; arthritis", "post-infectious arthritis", "Post-Infectious Arthritis", "Post Infectious Arthritis", "Arthritis, Postinfectious", "postdysenteric arthropathy", "Enteric reactive arthritis", "Post-infective arthropathy", "Arthritis, Post Infectious", "Post-bacterial arthropathy", "Arthritis, Post-Infectious", "Postinfectious Arthritides", "Postdysenteric arthropathy", "post-bacterial arthropathy", "Post-Infectious Arthritides", "Post dysenteric arthropathy", "postdysenteric; arthropathy", "Post-dysenteric arthropathy", "arthropathy; postdysenteric", "Reiter's syndrome (diagnosis)", "Reactive arthritis (disorder)", "Reiter's or Reactive arthritis", "Urethrooculoarticular syndrome", "reactive arthritis (diagnosis)", "dysentery; arthritis (etiology)", "Fiessinger-Leroy-Reiter syndrome", "ERA - Enteric reactive arthritis", "URETHRO-OCULO-ARTICULAR SYNDROME", "Fiessinger Leroy Reiter syndrome", "urethro-oculo-articular; syndrome", "syndrome; urethro-oculo-articular", "Reiter's syndrome with arthropathy", "ARTHRITIS, IDIOPATHIC BLENNORRHEAL", "Reiter's disease, site unspecified", "Reiter's disease, unspecified site", "Post-infective arthritis (disorder)", "Arthritis occurring after infection", "Reactive arthritis triad (disorder)", "Enteric acquired reactive arthritis", "Postdysenteric reactive arthropathy", "dysentery; arthritis (manifestation)", "Post-dysenteric reactive arthropathy", "post-infectious reactive arthropathy", "Post-bacterial arthropathy (disorder)", "postdysenteric arthropathy (diagnosis)", "Post-dysenteric arthropathy (disorder)", "Reiter's Syndrome or Reactive Arthritis", "EARA - Enteric acquired reactive arthritis", "Postdysenteric arthropathy, site unspecified", "Postdysenteric arthropathy, unspecified site", "Reiter's syndrome with arthropathy (diagnosis)", "infectious; arthritis, postinfective reaction (etiology)", "infectious; arthritis, postinfective reaction (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "reactive arthritis", "shortest_name_length": 4}
{"curie": "MONDO:0009956", "names": ["Red skin pigment, New Guinea type", "RED SKIN PIGMENT ANOMALY OF NEW GUINEA", "Red skin pigment anomaly of New Guinea", "red skin pigment anomaly of new guinea"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "red skin pigment anomaly of new guinea", "shortest_name_length": 33}
{"curie": "UMLS:C4687707", "names": ["Refractory Glioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Glioma", "shortest_name_length": 17}
{"curie": "MONDO:0018446", "names": ["autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome", "shortest_name_length": 83}
{"curie": "UMLS:C4763733", "names": ["Metastatic Lung Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Lung Neuroendocrine Neoplasm", "shortest_name_length": 39}
{"curie": "MONDO:0012641", "names": ["RLS5", "RLS 5", "restless legs syndrome 5", "RESTLESS LEGS SYNDROME, SUSCEPTIBILITY TO, 5", "restless legs syndrome, susceptibility to, 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "restless legs syndrome, susceptibility to, 5", "shortest_name_length": 4}
{"curie": "MONDO:0021032", "names": ["Herpes zoster eyelid dermatitis", "Herpes zoster dermatitis of eyelid", "Herpes Zoster Dermatitis of Eyelid", "herpes zoster dermatitis of eyelid", "Herpes zoster dermatitis of eyelids", "herpes zoster dermatitis of eyelids", "Herpes zoster with dermatitis of eyelid", "herpes zoster with dermatitis of eyelid", "Herpes zoster dermatitis of eyelid (diagnosis)", "Infection of skin of eyelid due to herpes zoster", "Infection of skin of eyelid due to herpes zoster (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "herpes zoster with dermatitis of eyelid", "shortest_name_length": 31}
{"curie": "UMLS:C4520759", "names": ["Stage III Larynx Epidermoid Carcinoma", "Stage III Larynx Squamous Cell Carcinoma", "Stage III Laryngeal Epidermoid Carcinoma", "Stage III Epidermoid Carcinoma of Larynx", "Stage III Laryngeal Squamous Cell Carcinoma", "Stage III Squamous Cell Carcinoma of Larynx", "Stage III Epidermoid Carcinoma of the Larynx", "Stage III Squamous Cell Carcinoma of the Larynx", "Stage III Laryngeal Throat Squamous Cell Cancer", "Stage III Laryngeal Squamous Cell Carcinoma AJCC v6", "Stage III Laryngeal Squamous Cell Carcinoma AJCC v7", "Stage III Laryngeal Squamous Cell Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Laryngeal Squamous Cell Carcinoma AJCC v6 and v7", "shortest_name_length": 37}
{"curie": "MONDO:0006956", "names": ["Rickettsiosis", "Rickettsioses", "rickettsiosis", "Rickettsiosis NOS", "Rickettsiae disease", "Rickettsial Disease", "Rickettsial disease", "rickettsial disease", "Rickettsial diseases", "Rickettsial Diseases", "Rickettsia Infection", "rickettsial diseases", "Rickettsia infection", "Rickettsial infection", "Infection, Rickettsia", "infection, Rickettsia", "Rickettsiales disease", "rickettsial infection", "Rickettsia Infections", "RICKETTSIAL INFECTIONS", "infections, Rickettsia", "Infections, Rickettsia", "Rickettsioses (A75-A79)", "Disease due to Rickettsia", "Rickettsial infection NOS", "rickettsiosis; Rickettsia", "Rickettsia; rickettsiosis", "Rickettsiosis, unspecified", "Rickettsial infection, NOS", "Disease due to Rickettsiales", "Disease caused by Rickettsia", "Rickettsia infectious disease", "Disease caused by rickettsiae", "Rickettsia disease or disorder", "Rickettsial Infectious Disease", "Diseases Caused by Rickettsiae", "Rickettsial infectious disease", "Disease caused by Rickettsiales", "Disease due to Genus Rickettsia", "Rickettsial Infectious Disorder", "Rickettsial disease (diagnosis)", "Rickettsial infectious disorder", "Rickettsial infectious disorders", "Disease caused by Rickettsia, NOS", "Disease caused by Genus Rickettsia", "Rickettsial infectious disease, NOS", "Rickettsia caused disease or disorder", "Disease caused by rickettsiae (disorder)", "Disease caused by Rickettsiales (disorder)", "Disease caused by Genus Rickettsia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rickettsiosis", "shortest_name_length": 13}
{"curie": "MONDO:0020530", "names": ["IFNGR1 deficiency", "interferon gamma, receptor 1, deficiency", "Interferon gamma, receptor 1, deficiency", "MSMD due to complete IFNgammaR1 deficiency", "MSMD due to complete interferon gamma receptor 1 deficiency", "Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR1 deficiency", "Mendelian susceptibility to mycobacterial diseases due to complete interferon gamma receptor 1 deficiency", "IFNGR1 autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency", "autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency caused by mutation in IFNGR1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR1 deficiency", "shortest_name_length": 17}
{"curie": "MONDO:0024250", "names": ["PLEVA", "pleva", "Mucha-Habermann", "Habermann disease", "disease, Habermann", "Habermanns disease", "Habermann's disease", "Acute parapsoriasis", "disease, Habermann's", "Mucha Habermann disease", "Mucha-Habermann Disease", "mucha-habermann disease", "Mucha-Habermann disease", "Mucha Habermann Disease", "mucha habermann disease", "mucha-habermann syndrome", "disease, Mucha-Habermann", "Disease, Mucha-Habermann", "Mucha-Habermann syndrome", "acute lichenoid pityriasis", "Acute lichenoid pityriasis", "Parapsoriasis varioliformis", "parapsoriasis varioliformis", "parapsoriasis; varioliformis", "Acute Pityriasis Lichenoides", "pityriasis lichenoides acuta", "Pityriasis lichenoides acuta", "varioliformis; parapsoriasis", "Pityriasis Lichenoides, Acute", "Acute vasculitic parapsoriasis", "parapsoriasis varioliformis acuta", "Parapsoriasis varioliformis acuta", "Acute parapsoriasis varioliformis", "acuta parapsoriasis varioliformis", "PLA - Pityriasis lichenoides acuta", "Acute lichenoid pityriasis (disorder)", "Parapsoriasis varioliformis (disorder)", "Pityriasis lichenoides et varioliformis acuta", "Pityriasis Lichenoides et Varioliformis Acuta", "pityriasis lichenoides et varioliformis acuta", "Parapsoriasis lichenoides et varioliformis acuta", "parapsoriasis lichenoides et varioliformis acuta", "pityriasis; lichenoides, et varioliformis (acuta)", "lichenoides; pityriasis, et varioliformis (acuta)", "PLEVA - Pityriasis lichenoides et varioliformis acuta", "pityriasis lichenoides et varioliformis acuta (diagnosis)", "Pityriasis lichenoides et varioliformis of Mucha-Habermann"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute lichenoid pityriasis", "shortest_name_length": 5}
{"curie": "MONDO:0007510", "names": ["ED2", "ECTD2", "Clouston", "HED2, FORMERLY", "clouston syndrome", "Clouston Syndrome", "Clouston syndrome", "CLOUSTON SYNDROME", "Cloustons Syndrome", "Syndrome, Clouston", "Clouston's syndrome", "Clouston's Syndrome", "Syndrome, Clouston's", "Patel Bixler syndrome", "Hydrotic Ectodermal Dysplasia", "Hidrotic Ectodermal Dysplasia", "hidrotic ectodermal dysplasia", "Hidrotic ectodermal dysplasia", "Dysplasia, Hidrotic Ectodermal", "Hidrotic Ectodermal Dysplasias", "ectodermal dysplasia, hidrotic", "ECTODERMAL DYSPLASIA, HIDROTIC", "Ectodermal Dysplasia, Hidrotic", "Ectodermal Dysplasia, Hydrotic", "Hydrotic Ectodermal Dysplasias", "Dysplasia, Hydrotic Ectodermal", "Dysplasias, Hidrotic Ectodermal", "ectodermal; dysplasia, hydrotic", "Dysplasias, Hydrotic Ectodermal", "Ectodermal Dysplasias, Hydrotic", "dysplasia; ectodermal, hydrotic", "Ectodermal Dysplasia 2, Hidrotic", "ectodermal dysplasia, hidrotic, 2", "ECTODERMAL DYSPLASIA 2, CLOUSTON TYPE", "ectodermal dysplasia 2, Clouston type", "CLOUSTON HIDROTIC ECTODERMAL DYSPLASIA", "Hidrotic ectodermal dysplasia syndrome", "Clouston Hidrotic Ectodermal Dysplasia", "Clouston hidrotic ectodermal dysplasia", "hidrotic ectodermal dysplasia syndrome", "Clouston's Hidrotic Ectodermal Dysplasia", "palmoplantar hyperkeratosis and alopecia", "Clouston's hidrotic ectodermal dysplasia", "ectodermal dysplasia, hidrotic, 2, formerly", "ECTODERMAL DYSPLASIA, HIDROTIC, 2, FORMERLY", "autosomal dominant hidrotic ectodermal dysplasia", "Autosomal Dominant Hidrotic Ectodermal Dysplasia", "Hidrotic ectodermal dysplasia syndrome (disorder)", "hidrotic ectodermal dysplasia, autosomal dominant", "Hidrotic Ectodermal Dysplasia, Autosomal Dominant", "Ectodermal Dysplasia, Hidrotic, Autosomal Dominant", "ECTODERMAL DYSPLASIA, HIDROTIC, AUTOSOMAL DOMINANT", "ectodermal dysplasia, hidrotic, autosomal dominant", "alopecia, dysplastic nails, palmar and plantar hyperkeratosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clouston syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0005936", "names": ["Lung Infection", "lung infection", "Lung infection", "lung; infection", "infection; lung", "Lung infection NOS", "pulmonary infection", "Recurrent pneumonia", "recurrent pneumonia", "Pulmonary infection", "Pneumonia recurrent", "PNEUMONIA RECURRENT", "pneumonia recurrent", "PULMONARY INFECTION", "pulmonary infections", "Pulmonary infections", "Pneumonia, recurrent", "infectious lung disease", "Infectious Lung Disease", "Infectious Lung Diseases", "Infectious Lung Disorder", "Infectious Lung Disorders", "Infectious disease of lung", "PULMONARY INFECTION MULTIPLE", "recurrent pneumonia (disease)", "Pneumonia, recurrent episodes", "Multiple pulmonary infections", "Recurrent pulmonary infection", "Recurrent pulmonary infections", "Recurrent pneumonia (disorder)", "Pulmonary infections, recurrent", "Recurrent episodes of pneumonia", "pulmonary infections, recurrent", "Recurrent pneumonia (diagnosis)", "pulmonary infections (diagnosis)", "Infectious disease of lung (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "recurrent pneumonia", "shortest_name_length": 14}
{"curie": "MONDO:0019621", "names": ["CPI", "chronic pneumonitis of infancy", "Chronic pneumonitis of infancy", "CPI - chronic pneumonitis of infancy", "Chronic pneumonitis of infancy (disorder)", "Chronic pneumonitis of infancy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic pneumonitis of infancy", "shortest_name_length": 3}
{"curie": "MONDO:0005688", "names": ["Campylobacterioses", "CAMPYLOBACTERIOSES", "Campylobacteriosis", "campylobacteriosis", "Campylobacter infection", "Campylobacter Infection", "campylobacter infection", "Campylobacteriosis, NOS", "Campylobacter; infection", "infection; Campylobacter", "Campylobacter Infections", "campylobacter infections", "Campylobacter infections", "Infection, Campylobacter", "Infections, Campylobacter", "Campylobacteriosis (disorder)", "Infection due to Campylobacter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "campylobacteriosis", "shortest_name_length": 18}
{"curie": "MONDO:0016439", "names": ["Elastoderma", "elastoderma", "Elastoderma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "elastoderma", "shortest_name_length": 11}
{"curie": "MONDO:0014361", "names": ["MRD26", "AUTS2 syndrome", "ASD due to AUTS2 deficiency", "intellectual disability type 26", "autosomal dominant mental retardation 26", "mental retardation, autosomal dominant 26", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 26", "mental retardation, autosomal dominant type 26", "autism spectrum disorder due to AUTS2 deficiency", "autosomal dominant intellectual developmental disorder 26", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 26", "intellectual developmental disorder, autosomal dominant 26", "autosomal dominant non-syndromic intellectual disability 26"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autism spectrum disorder due to AUTS2 deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0001340", "names": ["tumor heart", "Heart Tumor", "HEART TUMOR", "Heart tumor", "heart tumor", "Heart Cancer", "heart tumour", "Heart tumour", "heart tumors", "heart cancer", "Cardiac Tumor", "heart tumours", "Heart--Tumors", "Cardiac tumor", "Cardiac Tumors", "Tumor of Heart", "Tumor of heart", "tumor of heart", "Tumor, Cardiac", "Heart Neoplasm", "Heart Neoplasms", "tumour of heart", "Tumour of heart", "heart neoplasms", "Cardiac cancers", "Tumors, Cardiac", "cancer of heart", "Neoplasm, Heart", "cardiac neoplasm", "Cardiac Neoplasm", "Cardiac neoplasm", "Neoplasms, Heart", "cardiac neoplasms", "Neoplasm of heart", "Neoplasm, Cardiac", "Cardiac Neoplasms", "Cardiac neoplasia", "Neoplasm of Heart", "Cardiac neoplasms", "neoplasm of heart", "Tumor of the Heart", "Neoplasms, Cardiac", "Malignant Heart Tumor", "malignant heart tumor", "Neoplasm of the heart", "Neoplasm of the Heart", "Malignant Cardiac Tumor", "malignant Cardiac tumor", "Malignant Heart Neoplasm", "malignant tumor of heart", "Malignant tumor of heart", "Malignant Tumor of Heart", "malignant heart neoplasm", "Malignant tumour of heart", "Malignant Cardiac Neoplasm", "malignant Cardiac neoplasm", "Cardiac neoplasm malignant", "Cardiac Neoplasm, Malignant", "Malignant Neoplasm of Heart", "Cardiac neoplasm, malignant", "malignant neoplasm of heart", "Malignant neoplasm of heart", "Neoplasm of heart (disorder)", "malignant tumor of the heart", "Malignant Tumor of the Heart", "neoplasm of heart (diagnosis)", "Malignant cardiac neoplasm NOS", "Cardiac neoplasm malignant NOS", "malignant neoplasm of the heart", "Malignant Neoplasm of the Heart", "Malignant neoplasm of heart, NOS", "Malignant tumor of heart (disorder)", "malignant neoplasm of heart (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heart cancer", "shortest_name_length": 11}
{"curie": "MONDO:0001658", "names": ["goiter nontoxic", "Nontoxic goiter", "NONTOXIC GOITER", "Goitre nontoxic", "Nontoxic Goiter", "nontoxic goiter", "Goiter nontoxic", "Nontoxic goitre", "Non-toxic goitre", "nontoxic; goiter", "Non-toxic goiter", "non toxic goiter", "euthyroid goiter", "non-toxic goiter", "Non-toxic Goiter", "Euthyroid Goiter", "struma; nontoxic", "non-toxic goitre", "goitres non toxic", "goiter, non-toxic", "Goiter, non-toxic", "goiters non toxic", "goitre, non-toxic", "Goitre, non-toxic", "Simple nontoxic goiter", "Non-toxic simple goiter", "Nodule-thyroid, non tox", "non-toxic simple goitre", "Non-toxic simple goitre", "struma; nontoxic, simple", "nontoxic; goiter, simple", "nontoxic goiter (diagnosis)", "Nontoxic goiter, unspecified", "Nontoxic goitre, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nontoxic goiter", "shortest_name_length": 15}
{"curie": "UMLS:C3831024", "names": ["Congenital Hand and Foot Deformity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Hand and Foot Deformity", "shortest_name_length": 34}
{"curie": "UMLS:C3828505", "names": ["Postpartum Obstetric Thromboembolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postpartum Obstetric Thromboembolism", "shortest_name_length": 36}
{"curie": "MONDO:0007080", "names": ["GRA", "GSH", "FH1", "FH-I", "FH 1", "FH I", "HALD1", "CYP11B1/CYP11B2 Chimerism", "Familial Hyperaldosteronism Type 1", "Familial hyperaldosteronism type 1", "familial hyperaldosteronism type 1", "familial hyperaldosteronism type I", "Familial hyperaldosteronism type I", "hyperaldosteronism, familial type 1", "dexamethasone sensitive hypertension", "Hyperaldosteronism, Familial, Type I", "hyperaldosteronism, familial, type 1", "HYPERALDOSTERONISM, FAMILIAL, TYPE I", "Dexamethasone-sensitive hypertension", "hyperaldosteronism, familial, type I", "dexamethasone-sensitive hypertension", "glucocorticoid sensitive hypertension", "glucocorticoid-sensitive hypertension", "Glucocorticoid-sensitive hypertension", "GLUCOCORTICOID-REMEDIABLE ALDOSTERONISM", "Glucocorticoid Remediable Aldosteronism", "Glucocorticoid-Remediable Aldosteronism", "glucocorticoid-remediable aldosteronism", "Glucocorticoid-remediable aldosteronism", "aldosteronism, glucocorticoid-remediable", "Glucocorticoid Suppressible Hypertension", "aldosteronism, sensitive to dexamethasone", "ALDOSTERONISM, SENSITIVE TO DEXAMETHASONE", "Aldosteronism, Sensitive to Dexamethasone", "ACTH-dependent hyperaldosteronism syndrome", "ACTH-Dependent Hyperaldosteronism Syndrome", "ACTH-DEPENDENT HYPERALDOSTERONISM SYNDROME", "Familial hyperaldosteronism type 1 (disorder)", "GRA - glucocorticoid-remediable aldosteronism", "Glucocorticoid-Suppressible Hyperaldosteronism", "Glucocorticoid Suppressible Hyperaldosteronism", "glucocorticoid-suppressible hyperaldosteronism", "Glucocorticoid-suppressible hyperaldosteronism", "GLUCOCORTICOID-SUPPRESSIBLE HYPERALDOSTERONISM", "glucocorticoid-remediable aldosteronism (diagnosis)", "GSH - Glucocorticoid-suppressible hyperaldosteronism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glucocorticoid-remediable aldosteronism", "shortest_name_length": 3}
{"curie": "MONDO:0015403", "names": ["NICH", "Noninvoluting congenital hemangioma", "noninvoluting congenital hemangioma", "non-involuting congenital hemangioma", "Non-Involuting Congenital Hemangioma", "Non-involuting congenital hemangioma", "Noninvoluting congenital haemangioma", "Non-involuting congenital haemangioma", "NICH - noninvoluting congenital hemangioma", "NICH - non-involuting congenital hemangioma", "NICH - noninvoluting congenital haemangioma", "NICH - non-involuting congenital haemangioma", "Noninvoluting congenital hemangioma (disorder)", "Non-involuting congenital hemangioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-involuting congenital hemangioma", "shortest_name_length": 4}
{"curie": "MONDO:0032860", "names": ["MRT72", "autosomal recessive mental retardation 72", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 72", "Mental Retardation, Autosomal Recessive 72", "autosomal recessive intellectual developmental disorder-72", "autosomal recessive intellectual developmental disorder 72", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 72", "intellectual developmental disorder, autosomal recessive 72"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder, autosomal recessive 72", "shortest_name_length": 5}
{"curie": "MONDO:0001090", "names": ["Acute anterolateral myocardial infarction", "MYOCARDIAL INFARCTION ANTEROLATERAL ACUTE", "acute anterolateral myocardial infarction", "anterolateral myocardial infarction, acute", "acute myocardial infarction of anterolateral wall", "Acute myocardial infarction of anterolateral wall", "Acute myocardial infarction, of anterolateral wall", "acute anterolateral myocardial infarction (diagnosis)", "Acute myocardial infarction of anterolateral wall (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute anterolateral myocardial infarction", "shortest_name_length": 41}
{"curie": "MONDO:0009371", "names": ["3-hydroxyisobutyric aciduria", "3-HYDROXYISOBUTYRIC ACIDURIA", "3-Hydroxyisobutyric aciduria", "disorder of valine metabolism", "3-Hydroxyisobutyric aciduria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "3-hydroxyisobutyric aciduria", "shortest_name_length": 28}
{"curie": "MONDO:0024685", "names": ["Ph1-positive myeloid leukemia", "Ph1-Positive Myeloid Leukemia", "Ph1-Positive Myelocytic Leukemia", "Ph1-positive myelocytic leukemia", "Ph1-Positive Myelogenous Leukemia", "Ph1-positive myelogenous leukemia", "Ph1-Positive Granulocytic Leukemia", "Ph1-positive granulocytic leukemia", "Philadelphia-positive myeloid leukemia", "Philadelphia-Positive Myeloid Leukemia", "Philadelphia-Positive Myelocytic Leukemia", "Philadelphia-positive myelocytic leukemia", "Philadelphia-positive myelogenous leukemia", "Philadelphia-Positive Myelogenous Leukemia", "Philadelphia-positive granulocytic leukemia", "Philadelphia-Positive Granulocytic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Philadelphia-positive myelogenous leukemia", "shortest_name_length": 29}
{"curie": "MONDO:0016145", "names": ["dysferlinopathy", "Dysferlinopathy", "Qualitative or quantitative defects of dysferlin", "qualitative or quantitative defects of dysferlin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of dysferlin", "shortest_name_length": 15}
{"curie": "MONDO:0005551", "names": ["eye allergy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eye allergy", "shortest_name_length": 11}
{"curie": "MONDO:0002758", "names": ["vulva verrucous carcinoma", "Vulvar Verrucous Carcinoma", "vulvar verrucous carcinoma", "verrucous carcinoma of Vulva", "Verrucous Carcinoma of Vulva", "verrucous carcinoma of vulva", "verrucous carcinoma of the vulva", "Verrucous Carcinoma of the Vulva", "mammalian vulva verrucous carcinoma", "verrucous carcinoma of vulva (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulva verrucous carcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0018905", "names": ["DLBCL", "Histiocytic Lymphoma", "Lymphoma, Histiocytic", "Histiocytic Lymphomas", "Diffuse Large-Cell Lymphoma", "large cell diffuse lymphoma", "Diffuse Large Cell Lymphoma", "diffuse large cell lymphoma", "Lymphoma, Diffuse Large Cell", "Lymphoma, Diffuse Large-Cell", "Large Cell Lymphoma, Diffuse", "Large-Cell Lymphoma, Diffuse", "Diffuse Histiocytic Lymphoma", "Diffuse Large-Cell Lymphomas", "diffuse histiocytic lymphoma", "Diffuse large B-cell lymphoma", "Lymphoma, Diffuse Histiocytic", "Lymphoma, Large-Cell, Diffuse", "diffuse large b cell lymphoma", "Diffuse Large B Cell Lymphoma", "Noncleaved malignant lymphoma", "Diffuse Histiocytic Lymphomas", "diffuse large b-cell lymphoma", "Diffuse Large B-Cell Lymphoma", "lymphoma; diffuse, large cell", "diffuse; lymphoma, large cell", "Lymphoma, Large Cell, Diffuse", "Diffuse large B cell lymphoma", "Histiocytic Lymphoma, Diffuse", "diffuse large B-cell lymphoma", "Large cell malignant lymphoma", "lymphoma; large cell (diffuse)", "diffuse; lymphoma, histiocytic", "lymphoma; diffuse, histiocytic", "Diffuse large B-cell lymphomas", "Histiocytic malignant lymphoma", "Lymphoma, Histiocytic, Diffuse", "Lymphoma, Large B-Cell, Diffuse", "Diffuse, Large B-Cell, Lymphoma", "Large B-cell malignant lymphoma", "Large Lymphoid Lymphoma, Diffuse", "Centroblastic malignant lymphoma", "Lymphoma, Large Lymphoid, Diffuse", "Diffuse large B-cell lymphoma NOS", "DLBCL - diffuse large B cell lymphoma", "Diffuse Large B-Cell Lymphoma (DLBCL)", "Large cleaved cell malignant lymphoma", "Histiocytic diffuse malignant lymphoma", "Diffuse malignant lymphoma - large cell", "Malignant lymphoma, diffuse, large cell", "Diffuse large B cell malignant lymphoma", "Diffuse non-Hodgkin lymphoma, large cell", "Centroblastic diffuse malignant lymphoma", "Diffuse malignant lymphoma - histiocytic", "Malignant lymphoma, histiocytic, diffuse", "Large noncleaved cell malignant lymphoma", "Diffuse large B-cell lymphoma (diagnosis)", "Diffuse non-Hodgkin's lymphoma, large cell", "Diffuse large B-cell lymphoma (DLBCL), NOS", "Malignant lymphoma, large cell, diffuse NOS", "Large cell (diffuse) non-Hodgkin's lymphoma", "Malignant lymphoma, large cell, diffuse, NOS", "Lymphoma, diffuse large B cell, non Hodgkins", "Diffuse large cleaved cell malignant lymphoma", "Diffuse large noncleaved cell malignant lymphoma", "Centroblastic diffuse large B-cell malignant lymphoma", "Diffuse non-Hodgkin's lymphoma, large cell (clinical)", "Diffuse non-Hodgkin's lymphoma, large cell (disorder)", "Diffuse Large B-Cell Lymphoma, Not Otherwise Specified", "Malignant lymphoma, large cell, cleaved and noncleaved", "Malignant lymphoma - large cell cleaved and non-cleaved", "Large cleaved cell and noncleaved cell malignant lymphoma", "Diffuse large B cell malignant lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diffuse large B-cell lymphoma", "shortest_name_length": 5}
{"curie": "MONDO:0004758", "names": ["SCOTOMA", "scotoma", "Scotoma", "scotomas", "Scotomas", "scotomata", "SCOTOMATA", "blind spot", "Blind spot", "Blind Spot", "Optic Disk", "Spot, Blind", "Scotoma NOS", "blind spots", "Blind Spots", "Scotoma, NOS", "visual scotoma", "scotoma (symptom)", "scotoma (disease)", "Retina, blind spot", "visual blind spots", "Retinal blind spot", "enlarged blind spot", "Enlarged blind spot", "Blind spot enlarged", "Visual field scotoma", "defects field visual", "visual field scotoma", "enlarged angioscotoma", "Enlarged angioscotoma", "Blind spot area scotoma", "blind spot; enlargement", "enlargement; blind spot", "blind spot area scotoma", "Mariotte's spot enlarged", "scotoma of blind spot area", "Enlarged paracecal scotoma", "Scotoma of blind spot area", "enlarged paracaecal scotoma", "Enlarged paracaecal scotoma", "enlarged blind spot (___ mm)", "Enlarged blind spot (finding)", "Visual field scotoma (finding)", "Other localized visual field defect", "enlarged blind spot (physical finding)", "sector or arcuate visual field defects", "Sector or arcuate visual field defects", "Generalized visual field contraction or constriction", "generalized visual field contraction or constriction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scotoma", "shortest_name_length": 7}
{"curie": "UMLS:C5239365", "names": ["Refractory Anaplastic Oligodendroglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Anaplastic Oligodendroglioma", "shortest_name_length": 39}
{"curie": "MONDO:0004836", "names": ["Intravascular Fasciitis", "intravascular fasciitis", "Intravascular fasciitis", "intravascular nodular fasciitis", "Intravascular Nodular Fasciitis", "Intravascular fasciitis (disorder)", "Intravascular Pseudosarcomatous Fasciitis", "intravascular pseudosarcomatous fasciitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intravascular fasciitis", "shortest_name_length": 23}
{"curie": "UMLS:C0400990", "names": ["Biliary cyst", "biliary cyst", "Biliary Cyst", "biliary cysts", "cyst of biliary tract", "Cyst of biliary tract", "Cyst of biliary tract (disorder)", "cyst of biliary tract (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cyst of biliary tract", "shortest_name_length": 12}
{"curie": "MONDO:0005211", "names": ["Serous carcinoma", "serous ovarian cancer", "Ovarian Serous Carcinoma", "ovarian serous carcinoma", "serous carcinoma of ovary", "Serous Carcinoma of Ovary", "serous carcinoma of Ovary", "ovary serous adenocarcinoma", "ovarian serous adenocarcinoma", "serous carcinoma of the ovary", "Ovarian Serous Adenocarcinoma", "Serous Carcinoma of the Ovary", "ovarian adenocarcinoma serous", "Serous Adenocarcinoma of Ovary", "serous adenocarcinoma of ovary", "malignant ovarian serous tumor", "serous adenocarcinoma of the ovary", "Serous Adenocarcinoma of the Ovary", "serous adenocarcinoma of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian serous adenocarcinoma", "shortest_name_length": 16}
{"curie": "MONDO:0012747", "names": ["GSD12", "GSD 12", "GSD XII", "GSD type 12", "GSD type XII", "Aldoa deficiency", "ALDOA Deficiency", "ALDOA DEFICIENCY", "Glycogenosis type 12", "glycogenosis type 12", "Aldolase A deficiency", "Glycogenosis type XII", "Aldolase A Deficiency", "ALDOLASE A DEFICIENCY", "glycogenosis type XII", "aldolase a deficiency", "glycogen storage disease 12", "glycogen storage disease XII", "Red cell aldolase deficiency", "RED CELL ALDOLASE DEFICIENCY", "GLYCOGEN STORAGE DISEASE XII", "Glycogen Storage Disease XII", "Red Cell Aldolase Deficiency", "aldolase deficiency red cell", "Aldolase Deficiency, Red Cell", "aldolase deficiency, Red cell", "ALDOLASE DEFICIENCY, RED CELL", "HNSHA due to aldolase deficiency", "glycogen storage disease type 12", "GSD due to aldolase A deficiency", "Glycogen storage disease type 12", "glycogen storage disease type XII", "Glycogen storage disease type XII", "Glycogenosis due to aldolase A deficiency", "glycogenosis due to aldolase A deficiency", "glycogen storage disease due to aldolase A deficiency", "Glycogen storage disease due to aldolase A deficiency", "Glycogen storage disease due to aldolase A deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease due to aldolase A deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C0023656", "names": ["lichenoid drug reaction", "Lichenoid Drug Eruption", "Lichenoid drug eruption", "Lichenoid drug reaction", "drug eruptions lichenoid", "reaction; drug, lichenoid", "drug-induced lichen planus", "lichen planus drug-induced", "Drug-induced Lichen Planus", "Drug eruption lichen planus-like", "Lichenoid drug eruption (disorder)", "drug-induced lichen planus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lichenoid drug eruption", "shortest_name_length": 23}
{"curie": "MONDO:0010362", "names": ["GSD9D", "GSD Vb", "GSD IXD", "GSD IXd", "GSD type 9D", "GSD type 9E", "GSD type IXe", "GSD type IXd", "glycogenosis type 9D", "glycogenosis type 9E", "Glycogenosis type 9E", "Glycogenosis type 9D", "Glycogenosis type IXd", "Glycogenosis type IXe", "glycogenosis type IXe", "glycogenosis type IXd", "X-linked muscke glycogenosis", "GLYCOGEN STORAGE DISEASE IXd", "glycogen storage disease IXd", "Muscle Glycogenosis, X-Linked", "MUSCLE GLYCOGENOSIS, X-LINKED", "muscle glycogenosis, X-linked", "PHKA1 glycogen storage disease", "Glycogen storage disease type 9D", "Glycogen storage disease type 9E", "glycogen storage disease type 9E", "glycogen storage disease type 9D", "glycogen storage disease type IXd", "glycogen storage disease type IXe", "Glycogen storage disease type IXe", "Glycogen storage disease type IXd", "glycogen storage disease, type IXd", "Glycogen Storage Disease, Type IXD", "GLYCOGEN STORAGE DISEASE, TYPE IXd", "muscle phosphorylase kinase deficiency", "Muscle Phosphorylase Kinase Deficiency", "MUSCLE PHOSPHORYLASE KINASE DEFICIENCY", "muscle glycogenosis, X-linked recessive", "muscular phosphorylase kinase deficiency", "PHKA1-related glycogen storage disease type IX", "GSD due to muscle phosphorylase kinase deficiency", "glycogen storage disease caused by mutation in PHKA1", "Glycogenosis due to muscle phosphorylase kinase deficiency", "glycogenosis due to muscle phosphorylase kinase deficiency", "glycogen storage disease due to muscle phosphorylase kinase deficiency", "Glycogen storage disease due to muscle phosphorylase kinase deficiency", "Glycogen storage disease due to muscle phosphorylase kinase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease IXd", "shortest_name_length": 5}
{"curie": "UMLS:C3273219", "names": ["Condyloma with Dysplasia", "Condyloma Acuminatum with Dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Condyloma Acuminatum with Dysplasia", "shortest_name_length": 24}
{"curie": "MONDO:0014327", "names": ["PPKNEFD", "focal or diffuse nonepidermolytic palmoplantar keratoderma", "PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL OR DIFFUSE", "palmoplantar keratoderma, nonepidermolytic, focal or diffuse", "autosomal dominant focal non-epidermolytic palmoplantar keratoderma with plantar blistering"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "palmoplantar keratoderma, nonepidermolytic, focal or diffuse", "shortest_name_length": 7}
{"curie": "UMLS:C0152027", "names": ["Sensory disorder", "SENSORY DISORDER", "Sensory Disorder", "sensory disorder", "disorder sensory", "SENSORY DISORDERS", "sensory disorders", "Sensory Disorders", "Sensory disorders", "Sensory disturbance", "SENSORY DISTURBANCE", "sensory disturbance", "Sensory disturbances", "disturbances sensory", "sensory disturbances", "Sensory disorder, NOS", "Neurosensory Disorder", "sensory function defect", "sensory system disorder", "Sensory disturbance NOS", "Sensory disturbance, NOS", "Sensory System Disorders", "sensory disorder diagnosis", "Sensory disorder (disorder)", "Sensory disease or syndrome", "sensory disorder (diagnosis)", "sensory disturbances (symptom)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sensory Disorders", "shortest_name_length": 16}
{"curie": "MONDO:0014476", "names": ["EA8", "episodic ataxia type 8", "Episodic ataxia type 8", "EPISODIC ATAXIA, TYPE 8", "episodic ataxia, type 8", "episodic ataxia with slurred speech", "Episodic ataxia with slurred speech", "Episodic ataxia with slurred speech (disorder)", "ataxia hereditary episodic with slurred speech", "Episodic ataxia with slurred speech (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "episodic ataxia type 8", "shortest_name_length": 3}
{"curie": "MONDO:0020640", "names": ["Autoimmune Encephalitis", "autoimmune encephalitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune encephalitis", "shortest_name_length": 23}
{"curie": "MONDO:0008150", "names": ["OGD", "Fairbank-Keats syndrome", "osteoglophonic dwarfism", "OSTEOGLOPHONIC DWARFISM", "Osteoglophonic dwarfism", "Osteoglophonic dysplasia", "osteoglophonic dysplasia", "OSTEOGLOPHONIC dysplasia", "OSTEOGLOPHONIC DYSPLASIA", "Osteoglosphonic dysplasia", "Osteoglophonic dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteoglophonic dwarfism", "shortest_name_length": 3}
{"curie": "MONDO:0056815", "names": ["liver adenosquamous cancer", "Liver Adenosquamous Cancer", "Liver Adenosquamous Carcinoma", "liver adenosquamous carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "liver adenosquamous carcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0001744", "names": ["close angle glaucoma", "NARROW ANGLE GLAUCOMA", "glaucoma; obstructive", "glaucoma narrow angle", "obstructive; glaucoma", "glaucoma closed angle", "Closed angle glaucoma", "Angle glaucoma closed", "GLAUCOMA NARROW ANGLE", "Narrow Angle Glaucoma", "closed-angle glaucoma", "Narrow angle glaucoma", "GLAUCOMA, OBSTRUCTIVE", "narrow angle glaucoma", "Closed Angle Glaucoma", "Narrow cleft glaucoma", "narrow-angle glaucoma", "Glaucoma closed angle", "closed angle glaucoma", "narrow glaucoma angle", "Narrow-angle glaucoma", "Narrow-Angle Glaucoma", "Closed-Angle Glaucoma", "angles glaucoma narrow", "narrow angle; glaucoma", "Glaucoma, Narrow Angle", "GLAUCOMA, NARROW ANGLE", "Glaucoma, Closed Angle", "angle-closure glaucoma", "Uncompensated Glaucoma", "GLAUCOMA, CLOSED ANGLE", "Angle-closure glaucoma", "Closure-angle glaucoma", "Angle-Closure Glaucoma", "glaucoma angle-closure", "glaucoma; narrow angle", "Angle closure glaucoma", "angle closure glaucoma", "Glaucoma, Narrow-Angle", "Glaucoma, Closed-Angle", "Narrow-Angle Glaucomas", "Closed-Angle Glaucomas", "Angle Closure Glaucoma", "Angle Closure Glaucomas", "Glaucoma, Angle-Closure", "Uncompensated Glaucomas", "Glaucomas, Narrow-Angle", "Glaucoma, angle-closure", "Uncompensative Glaucoma", "Glaucomas, Closed-Angle", "Glaucoma, Uncompensated", "angle-closure; glaucoma", "Glaucoma, Angle Closure", "glaucoma; angle-closure", "Angle-Closure Glaucomas", "Glaucomas, Uncompensated", "Glaucoma, Uncompensative", "Glaucomas, Angle-Closure", "Uncompensative Glaucomas", "Glaucomas, Angle Closure", "Glaucomas, Uncompensative", "ACG - Angle-closure glaucoma", "ACG - angle-closure glaucoma", "ACG - Angle closure glaucoma", "obsolete Narrow angle glaucoma", "Primary Angle Closure Glaucoma", "Angle-closure glaucoma, primary", "Angle-closure glaucoma (disorder)", "angle-closure glaucoma (diagnosis)", "primary open-angle glaucoma with narrow angles"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angle-closure glaucoma", "shortest_name_length": 20}
{"curie": "MONDO:0030995", "names": ["GDSBA", "global developmental delay with speech and behavioral abnormalities", "GLOBAL DEVELOPMENTAL DELAY WITH SPEECH AND BEHAVIORAL ABNORMALITIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "global developmental delay with speech and behavioral abnormalities", "shortest_name_length": 5}
{"curie": "MONDO:0002787", "names": ["ACP", "Adamantinous craniopharyngioma", "Adamantinous Craniopharyngioma", "adamantinous craniopharyngioma", "Adamantinous Craniopharyngiomas", "Craniopharyngioma, Adamantinous", "Craniopharyngiomas, Adamantinous", "Adamantinous Rathke's Pouch tumor", "Adamantinous Rathke's Pouch Tumor", "adamantinous Rathke's pouch tumor", "adamantinomatous craniopharyngioma", "Adamantinomatous Craniopharyngioma", "Adamantinomatous craniopharyngioma", "Craniopharyngioma, adamantinomatous", "craniopharyngioma, adamantinomatous", "Adamantinous Rathke's Pouch Neoplasm", "adamantinous tumor of Rathke's pouch", "Adamantinous Tumor of Rathke's Pouch", "adamantinous Rathke's pouch neoplasm", "Adamantinous Neoplasm of Rathke's Pouch", "adamantinous neoplasm of Rathke's pouch", "adamantinous craniopharyngioma (morphologic abnormality)", "Craniopharyngioma, adamantinomatous (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adamantinous craniopharyngioma", "shortest_name_length": 3}
{"curie": "MONDO:0100097", "names": ["CAD due to TBX4", "congenital alveolar dysplasia due to TBX4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital alveolar dysplasia due to TBX4", "shortest_name_length": 15}
{"curie": "UMLS:C0854742", "names": ["Recurrent AIDS-Related Anal Cancer", "AIDS-related anal cancer recurrent", "Recurrent AIDS-Related Anal Carcinoma", "Recurrent AIDS-Related Anal Canal Cancer", "Recurrent AIDS-Related Anal Canal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-related anal cancer recurrent", "shortest_name_length": 34}
{"curie": "MONDO:0015793", "names": ["moderate multiminicore disease with hand involvement", "Moderate multiminicore disease with hand involvement", "Multiminicore Disease, Moderate, with Hand Involvement", "MULTIMINICORE DISEASE, MODERATE, WITH HAND INVOLVEMENT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "moderate multiminicore disease with hand involvement", "shortest_name_length": 52}
{"curie": "MONDO:0025484", "names": ["said", "SAIDS", "saids", "Simian AIDS", "simian AIDS", "AIDS, Simian", "Simian AIDSs", "AIDSs, Simian", "simian lymphoproliferative syndrome", "Simian Acquired Immunodeficiency Syndrome", "simian acquired immunodeficiency syndrome", "Simian acquired immuno deficiency syndrome", "Simian Acquired Immuno Deficiency Syndrome", "Simian Acquired Immuno-Deficiency Syndrome", "Simian Acquired Immune Deficiency Syndrome", "Simian acquired immuno-deficiency syndrome", "Simian acquired immune deficiency syndrome", "Simian immunodeficiency virus monkey disease", "Simian immunodeficiency virus caused monkey disease", "Simian acquired immune deficiency syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "simian acquired immunodeficiency syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0000001", "names": ["DISEASE", "Disease", "disease", "diseases", "Disorder", "disorder", "Diseases", "Disorders", "condition", "Diagnosis", "disorders", "disease_type", "disease term", "disease_term", "disease type", "Disease, NOS", "Other Disease", "Disorder, NOS", "other disease", "disease/disorder", "medical condition", "Disease (disorder)", "disease or disorder", "Disease or Disorder", "disease (or disorder)", "Diseases and Disorders", "diseases and disorders", "Disease or syndrome present", "Clinical disease or syndrome", "Disease or syndrome present, NOS", "Clinical disease AND/OR syndrome", "Clinical disease or syndrome, NOS", "disease or disorder, non-neoplastic", "Disease or Disorder, Non-Neoplastic", "diagnoses, syndromes, and conditions", "Clinical disease or syndrome present", "Clinical disease or syndrome present, NOS", "diagnoses, syndromes, and conditions (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disease", "shortest_name_length": 7}
{"curie": "UMLS:C4763836", "names": ["Metastatic Bladder Large Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Bladder Large Cell Neuroendocrine Carcinoma", "shortest_name_length": 54}
{"curie": "MONDO:0019771", "names": ["oromandibular dystonia", "Isolated oromandibular dystonia", "Isolated oromandibular dystonia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oromandibular dystonia", "shortest_name_length": 22}
{"curie": "MONDO:0014066", "names": ["MC3DN5", "UQCRC2 mitochondrial complex III deficiency", "mitochondrial Complex 3 deficiency, nuclear type 5", "mitochondrial complex III deficiency nuclear type 5", "MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 5", "mitochondrial complex III deficiency, nuclear type 5", "mitochondrial complex III deficiency caused by mutation in UQCRC2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex III deficiency nuclear type 5", "shortest_name_length": 6}
{"curie": "MONDO:0013512", "names": ["HbH", "HBH", "HbH disease", "Hemoglobin H", "Haemoglobin H", "HbH hemoglobin", "HbH haemoglobin", "HEMOGLOBIN H DISEASE", "HEMOGLOBIN H disease", "Hemoglobin H Disease", "hemoglobin H disease", "Hemoglobin H disease", "haemoglobin H disease", "Haemoglobin H disease", "alpha-thalassemia intermedia", "Alpha-thalassemia intermedia", "Alpha thalassemia intermedia", "Alpha thalassaemia intermedia", "Hemoglobin H disease (disorder)", "Hemoglobin H disease, Deletional", "hemoglobin H disease, deletional", "HEMOGLOBIN H DISEASE, DELETIONAL", "hemoglobin H disease (diagnosis)", "haemoglobin H disease, deletional", "HEMOGLOBIN H DISEASE, NONDELETIONAL", "Hemoglobin H disease, Nondeletional", "Alpha-thalassemia, Hemoglobin H type", "alpha thalassemia, hemoglobin H type", "ALPHA-THALASSEMIA, HEMOGLOBIN H TYPE", "alpha thalassemia, haemoglobin H type", "alpha Thalassemia, hemoglobin H disease", "hemoglobin H disease, deletional and nondeletional"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemoglobin H disease", "shortest_name_length": 3}
{"curie": "MONDO:0012407", "names": ["PNPOD", "Pnpo deficiency", "PNPO Deficiency", "PNPO deficiency", "PNPO DEFICIENCY", "pyridoxamine 5'-oxidase deficiency", "Pyridoxamine 5'-oxidase deficiency", "Pyridoxal phosphate-dependent seizures", "pyridoxal phosphate-dependent seizures", "pyridoxal phosphate-responsive seizures", "Pyridoxal phosphate-responsive seizures", "epilepsy pyridoxal 5-phosphate dependent", "Pyridoxal 5-phosphate dependent epilepsy", "pyridoxal 5'-phosphate-dependent epilepsy", "Pyridoxal 5'-Phosphate-Dependent Epilepsy", "pyridoxine 5' phosphate oxidase deficiency", "pyridoxine-5'-phosphate oxidase deficiency", "Pyridoxine-5'-Phosphate Oxidase Deficiency", "pyridoxamine 5'-phosphate oxidase deficiency", "Pyridoxamine 5'-phosphate oxidase deficiency", "Seizures, Pyridoxine-Resistant, PLP-Sensitive", "seizures, pyridoxine-resistant, PLP-sensitive", "SEIZURES, PYRIDOXINE-RESISTANT, PLP-SENSITIVE", "PNPO-Related Neonatal Epileptic Encephalopathy", "PNPO-related neonatal epileptic encephalopathy", "EPILEPTIC ENCEPHALOPATHY, NEONATAL, PNPO-RELATED", "epileptic encephalopathy, neonatal, Pnpo-related", "Epileptic Encephalopathy, Neonatal, PNPO-Related", "Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency", "PYRIDOXAMINE 5-PRIME-PHOSPHATE OXIDASE DEFICIENCY", "pyridoxamine 5-prime-phosphate oxidase deficiency", "Pyridoxal 5-phosphate dependent epilepsy (disorder)", "Pyridoxal 5-phosphate dependent epilepsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyridoxal phosphate-responsive seizures", "shortest_name_length": 5}
{"curie": "UMLS:C0948976", "names": ["Leukemia cutis", "leukemia cutis", "Leukemia Cutis", "Leukaemia cutis", "leukaemia cutis", "Leukemic infiltration of skin", "Leukaemic infiltration of skin", "Leukemic infiltration of skin (disorder)", "Leukemic infiltration of skin (diagnosis)", "skin neoplasm malignant secondary leukemic infiltration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leukemic infiltration of skin", "shortest_name_length": 14}
{"curie": "UMLS:C1709024", "names": ["Micronodular Thymoma", "Micronodular Thymoma with Lymphoid Stroma", "Micronodular thymoma with lymphoid stroma", "Micronodular Thymoma with Lymphoid B-Cell Hyperplasia", "Micronodular thymoma with lymphoid stroma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Micronodular thymoma with lymphoid stroma", "shortest_name_length": 20}
{"curie": "MONDO:0017089", "names": ["isolated macrencephaly", "isolated megalencephaly", "isolated megalencephaly (disease)", "nonsyndromic megalencephaly (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated megalencephaly", "shortest_name_length": 22}
{"curie": "MONDO:0022647", "names": ["cardiomelic syndrome stratton Koehler type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiomelic syndrome stratton Koehler type", "shortest_name_length": 42}
{"curie": "MONDO:0019949", "names": ["Zebra body myopathy", "zebra body myopathy", "Zebra body myopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "zebra body myopathy", "shortest_name_length": 19}
{"curie": "MONDO:0014628", "names": ["IBGC6", "BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 6", "basal ganglia calcification, idiopathic, 6", "XPR1 bilateral striopallidodentate calcinosis", "basal ganglia calcification, idiopathic, type 6", "bilateral striopallidodentate calcinosis caused by mutation in XPR1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "basal ganglia calcification, idiopathic, 6", "shortest_name_length": 5}
{"curie": "UMLS:C0000846", "names": ["APLASIA", "agenesis", "Agenesis", "Agenesis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Agenesis", "shortest_name_length": 7}
{"curie": "MONDO:0005517", "names": ["Pharynx Tumor", "Pharnyx Cancer", "Pharynx Cancer", "pharynx tumors", "pharynx cancer", "cancer pharynx", "Pharynx Cancers", "Pharnyx Cancers", "Cancer, Pharnyx", "Pharynx--Cancer", "Pharynx--Tumors", "pharynx tumours", "Pharyngeal Tumor", "Tumor of Pharynx", "Tumor of pharynx", "Pharynx Neoplasm", "Cancers, Pharnyx", "pharynx neoplasm", "Cancer of Pharynx", "Pharyngeal cancer", "Cancer of pharynx", "Tumour of pharynx", "cancer pharyngeal", "Neoplasm, Pharynx", "pharyngeal cancer", "pharynx neoplasms", "Pharyngeal Cancer", "Pharynx Neoplasms", "cancer of pharynx", "Neoplasms, Pharynx", "pharyngeal cancers", "Pharyngeal Cancers", "Cancer, Pharyngeal", "Pharyngeal Neoplasm", "Neoplasm of pharynx", "Cancers, Pharyngeal", "Neoplasm of Pharynx", "neoplasm of pharynx", "pharyngeal neoplasm", "Pharyngeal neoplasm", "Tumor of the pharynx", "Tumor of the Pharynx", "Neoplasm, Pharyngeal", "Pharyngeal Neoplasms", "cancer of the pharynx", "Tumour of the pharynx", "Neoplasms, Pharyngeal", "Cancer of the Pharynx", "CA - Cancer of pharynx", "neoplasm of the throat", "chordate pharynx cancer", "Neoplasm of the pharynx", "Neoplasm of the Pharynx", "Malignant Pharynx Tumor", "malignant pharynx tumor", "pharynx tumor or cancer", "Pharyngeal neoplasm NOS", "Neoplasia of the pharynx", "Malignant Pharynx Neoplasm", "malignant pharyngeal tumor", "pharyngeal tumor or cancer", "cancer of chordate pharynx", "Pharynx neoplasm malignant", "Malignant tumor of pharynx", "malignant pharynx neoplasm", "PHARYNX NEOPLASM MALIGNANT", "Malignant Tumor of Pharynx", "malignant tumor of pharynx", "Malignant Pharyngeal Tumor", "Malignant tumour of pharynx", "Malignant neoplasm of pharynx", "Malignant Pharyngeal Neoplasm", "malignant pharyngeal neoplasm", "malignant neoplasm of pharynx", "Malignant Tumor of the Pharynx", "Neoplasm of pharynx (disorder)", "malignant tumor of the pharynx", "neoplasm of pharynx (diagnosis)", "Malignant neoplasm of pharynx, NOS", "neoplasm of the throat (diagnosis)", "malignant chordate pharynx neoplasm", "Pharyngeal cancer stage unspecified", "malignant neoplasm of chordate pharynx", "Malignant neoplasm of pharynx (disorder)", "malignant neoplasm of pharynx (diagnosis)", "Malignant neoplasm of pharynx, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pharynx cancer", "shortest_name_length": 13}
{"curie": "MONDO:0026045", "names": ["prurigo nodularis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prurigo nodularis", "shortest_name_length": 17}
{"curie": "UMLS:C4521789", "names": ["Stage III Gastric (Stomach) Cancer", "Pathologic Stage III Gastric Cancer AJCC v8", "Pathologic Stage III Gastric Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage III Gastric Cancer AJCC v8", "shortest_name_length": 34}
{"curie": "MONDO:0010902", "names": ["Spondyloepiphyseal dysplasia Reardon type", "spondyloepiphyseal dysplasia, Reardon type", "Spondyloepiphyseal dysplasia, Reardon type", "Spondyloepiphyseal dysplasia Reardon type (disorder)", "SPONDYLOEPIPHYSEAL DYSPLASIA WITH ATLANTOAXIAL INSTABILITY", "spondyloepiphyseal dysplasia with atlantoaxial instability", "Spondyloepiphyseal Dysplasia with Atlantoaxial Instability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepiphyseal dysplasia, Reardon type", "shortest_name_length": 41}
{"curie": "UMLS:C4764278", "names": ["Unresectable Bladder Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Bladder Urothelial Carcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0000923", "names": ["PIE", "pie", "Soft tissue emphysema", "emphysema subcutaneous", "interstitial emphysema", "Subcutaneous emphysema", "Subcutaneous Emphysema", "Interstitial emphysema", "emphysema interstitial", "SUBCUTANEOUS EMPHYSEMA", "subcutaneous emphysema", "Subcutaneous Emphysemas", "Emphysema, Subcutaneous", "emphysema; subcutaneous", "subcutaneous; emphysema", "interstitial; emphysema", "Emphysema, interstitial", "EMPHYSEMA, SUBCUTANEOUS", "emphysema; interstitial", "Emphysemas, Subcutaneous", "Interstitial Emphysema of Lung", "interstitial emphysema of lung", "Interstitial emphysema of lung", "Pulmonary Interstitial Emphysema", "Interstitial pulmonary emphysema", "pulmonary interstitial emphysema", "Subcutaneous emphysema (disorder)", "interstitial emphysema (diagnosis)", "Interstitial emphysema of lung (disorder)", "Interstitial emphysema (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "interstitial emphysema", "shortest_name_length": 3}
{"curie": "MONDO:0004936", "names": ["inversion uterus", "Uterus Inversion", "Uterine Inversion", "UTERINE INVERSION", "Uterine inversion", "uterus; inversion", "inversion uterine", "uterine inversion", "inversion; uterus", "Inversion, Uterine", "Inversion of Uterus", "Inversion of uterus", "inversion of uterus", "Uterine inversion, NOS", "Uterine inversion (disorder)", "uterine inversion (diagnosis)", "Obstetrical inversion of uterus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine inversion", "shortest_name_length": 16}
{"curie": "UMLS:C4683744", "names": ["Stage IIB Mycosis Fungoides and Sezary Syndrome AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Mycosis Fungoides and Sezary Syndrome AJCC v8", "shortest_name_length": 55}
{"curie": "UMLS:C0854504", "names": ["Enterococcal bacteremia", "Enterococcal bacteraemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Enterococcal bacteremia", "shortest_name_length": 23}
{"curie": "MONDO:0017788", "names": ["Dinno syndrome", "contractures - webbed neck - micrognathia - hypoplastic nipples syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "contractures - webbed neck - micrognathia - hypoplastic nipples syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0005066", "names": ["Thesaurismosis", "RNDx metabolic", "Thesaurismoses", "Metabolic Disease", "metabolic disease", "Metabolic disease", "Metabolic Disorder", "Disorder;metabolic", "metabolic disorder", "metabolic diseases", "Disease, Metabolic", "Metabolic disorder", "Metabolic Diseases", "METABOLIC DISORDERS", "metabolic disorders", "Metabolic Disorders", "Metabolic disorders", "metabolism disorder", "Diseases, Metabolic", "disorder; metabolism", "metabolism; disorder", "Metabolism Disorders", "Metabolic derangement", "Metabolism--Disorders", "disease of metabolism", "Metabolic disease, NOS", "Metabolic disorder NOS", "Metabolic disorder, NOS", "MD - Metabolic disorders", "metabolic process disease", "RNDx metabolic (diagnosis)", "general; metabolic disorder", "metabolic disorder; general", "Metabolic disease (disorder)", "METABOLIC DISORDERS: GENERAL", "disorder of metabolic process", "metabolism; disorder, general", "Generalized metabolic disorder", "Generalised metabolic disorder", "Metabolic disorder, unspecified", "metabolic disorders (diagnosis)", "Unspecified disorder of metabolism", "Generalized metabolic disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metabolic disease", "shortest_name_length": 14}
{"curie": "MONDO:0031169", "names": ["odontochondrodysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "odontochondrodysplasia", "shortest_name_length": 22}
{"curie": "MONDO:0011134", "names": ["CRJS", "curry Jones syndrome", "curry-Jones syndrome", "Curry-Jones Syndrome", "CURRY-JONES SYNDROME", "curry-JONES syndrome", "Curry Jones syndrome", "Curry-Jones syndrome", "Curry Jones syndrome (disorder)", "Winter Shortland Temple syndrome", "Curry-Jones syndrome, somatic mosaic", "corpus callosum agenesis polysyndactyly", "corpus callosum agenesis-polysyndactyly syndrome", "Corpus callosum agenesis-polysyndactyly syndrome", "Agenesis of corpus callosum with polysyndactyly syndrome", "craniofacial malformations, asymmetric, with polysyndactyly and abnormal skin and gut development", "Craniofacial malformations, asymmetric, with polysyndactyly and abnormal skin and gut development", "CRANIOFACIAL MALFORMATIONS, ASYMMETRIC, WITH POLYSYNDACTYLY AND ABNORMAL SKIN AND GUT DEVELOPMENT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Curry-Jones syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C4054601", "names": ["Undifferentiated High Grade Pleomorphic Sarcoma of Bone", "Localized Adult Undifferentiated High Grade Pleomorphic Sarcoma", "Localized Adult Undifferentiated High Grade Pleomorphic Sarcoma of Bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized Adult Undifferentiated High Grade Pleomorphic Sarcoma of Bone", "shortest_name_length": 55}
{"curie": "MONDO:0004643", "names": ["myelosis", "myeloid leukemia", "Leukemia Myeloid", "Myeloid Leukemia", "leukemia myeloid", "Myeloid leukemia", "LEUKEMIA MYELOID", "Leukemia myeloid", "LEUKAEMIA MYELOID", "Myeloid leukemias", "myeloid; leukemia", "Leukemia, Myeloid", "Leukaemia myeloid", "Myeloid leukaemia", "myeloid leukaemia", "Myeloid Leukemias", "leukemia; myeloid", "Myeloid leukaemias", "Leukemias, Myeloid", "Myelocytic Leukemia", "Myelocytic leukemia", "leukemia myelocytic", "myelocytic leukemia", "Myelogenous leukemia", "myelocytic leukaemia", "myelogenous leukemia", "Myelocytic Leukemias", "Myeloid leukemia NOS", "[M]Myeloid leukemias", "leukemia myelogenous", "Leukemia myelogenous", "myelocytic; leukemia", "LEUKEMIA MYELOGENOUS", "Leukemia, Myelocytic", "leukemia; myelocytic", "Myelogenous Leukemia", "Myelocytic leukaemia", "Myelogenous Leukemias", "myelogenous leukaemia", "Myeloid leukaemia NOS", "Granulocytic Leukemia", "Leukaemia myelogenous", "granulocytic leukemia", "Myelogenous leukaemia", "Leukemia granulocytic", "Myeloid leukemia, NOS", "Leukemias, Myelocytic", "LEUKAEMIA MYELOGENOUS", "LEUKEMIA GRANULOCYTIC", "leukaemia myelogenous", "Leukemia, Myelogenous", "Leukemia Granulocytic", "leukemia granulocytic", "[M]Myeloid leukaemias", "Granulocytic leukemia", "Leukemias, Myelogenous", "Leukaemia granulocytic", "Myeloid leukaemia, NOS", "granulocytic; leukemia", "Leukemia, Granulocytic", "Granulocytic Leukemias", "LEUKAEMIA GRANULOCYTIC", "Granulocytic leukaemia", "granulocytic leukaemia", "leukemia; granulocytic", "Leukemias, Granulocytic", "Myelocytic leukemia, NOS", "Non-lymphocytic Leukemia", "Non-lymphocytic leukemia", "non-lymphocytic leukemia", "Non-Lymphocytic Leukemia", "Myelocytic leukaemia, NOS", "Myelogenous leukemia, NOS", "Non-lymphocytic leukaemia", "Leukemia granulocytic NOS", "Non-Lymphoblastic Leukemia", "Myelogenous leukaemia, NOS", "non-lymphoblastic leukemia", "Leukaemia granulocytic NOS", "Granulocytic leukemia, NOS", "Non-lymphoblastic Leukemia", "Myeloid leukemia (disorder)", "Granulocytic leukaemia, NOS", "Unspecified myeloid leukemia", "Myeloid leukemia, unspecified", "myeloid granulocytic leukemia", "Unspecified myeloid leukaemia", "Non-lymphoblastic leukemia NOS", "myeloid granulocytic leukaemia", "Myeloid leukaemia, unspecified", "Non-lymphoblastic leukaemia NOS", "MYELOID (GRANULOCYTIC) LEUKEMIAS", "Granulocytic leukemia (disorder)", "myelogenous leukemia (diagnosis)", "LEUKEMIA, GRANULOCYTIC, MALIGNANT", "Myeloid leukemia, unspecified NOS", "leukemia, granulocytic, malignant", "Myeloid leukemia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myeloid leukemia", "shortest_name_length": 8}
{"curie": "UMLS:C1336494", "names": ["I", "Stage I Uveal Melanoma", "Stage I Melanoma of Uvea", "Stage I Melanoma of the Uvea", "Stage I Uveal Melanoma AJCC v7", "Stage I Uveal Malignant Melanoma", "Stage I Malignant Melanoma of Uvea", "Stage I Malignant Melanoma of the Uvea"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Uveal Melanoma AJCC v7", "shortest_name_length": 1}
{"curie": "UMLS:C0684817", "names": ["NECK METASTASIS", "Metastases to Neck", "Metastases to neck", "Metastasis to the Neck", "Metastatic Tumor to the Neck", "Metastatic Neoplasm to the Neck", "malignant neoplasm of neck secondary", "Secondary malignant neoplasm of neck", "Metastatic malignant neoplasm of neck", "Metastatic malignant neoplasm to neck", "Secondary malignant neoplasm of neck, NOS", "Metastatic Malignant Neoplasm to the Neck", "Metastatic Malignant Neoplasm in the Neck", "Metastatic malignant neoplasm to neck, NOS", "Secondary malignant neoplasm of neck (diagnosis)", "Metastatic malignant neoplasm to neck (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to neck", "shortest_name_length": 15}
{"curie": "MONDO:0015756", "names": ["myeloid hemopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myeloid hemopathy", "shortest_name_length": 17}
{"curie": "MONDO:0015961", "names": ["genetic head and neck malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genetic head and neck malformation", "shortest_name_length": 34}
{"curie": "MONDO:0011557", "names": ["radiation sensitivity/chromosome instability syndrome, autosomal dominant", "RADIATION SENSITIVITY/CHROMOSOME INSTABILITY SYNDROME, AUTOSOMAL DOMINANT", "Radiation Sensitivity Chromosome Instability Syndrome, Autosomal Dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radiation sensitivity/chromosome instability syndrome, autosomal dominant", "shortest_name_length": 73}
{"curie": "EFO:0004609", "names": ["treatment refractory schizophrenia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "treatment refractory schizophrenia", "shortest_name_length": 34}
{"curie": "MONDO:0025356", "names": ["OAZON", "azoospermia, obstructive, with nephrolithiasis", "AZOOSPERMIA, OBSTRUCTIVE, WITH NEPHROLITHIASIS", "azoospermia, obstructive, with nephrolithiasis, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "azoospermia, obstructive, with nephrolithiasis", "shortest_name_length": 5}
{"curie": "MONDO:0012387", "names": ["osteosclerosis with ichthyosis and POF", "OSTEOSCLEROSIS WITH ICHTHYOSIS AND PREMATURE OVARIAN FAILURE", "Osteosclerosis-ichthyosis-premature ovarian failure syndrome", "osteosclerosis-ichthyosis-premature ovarian failure syndrome", "osteosclerosis with ichthyosis and premature ovarian failure", "Osteosclerosis with ichthyosis and premature ovarian failure", "Osteosclerosis, ichthyosis, premature ovarian failure syndrome", "sclerosing dysplasia of bone-ichthyosis-premature ovarian failure syndrome", "Sclerosing dysplasia of bone with ichthyosis and premature ovarian failure", "sclerosing dysplasia of bone with ichthyosis and premature ovarian failure", "SCLEROSING DYSPLASIA OF BONE WITH ICHTHYOSIS AND PREMATURE OVARIAN FAILURE", "Sclerosing dysplasia of bone-ichthyosis-premature ovarian failure syndrome", "Sclerosing dysplasia of bone, ichthyosis, premature ovarian failure syndrome", "Sclerosing dysplasia of bone, ichthyosis, premature ovarian failure syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteosclerosis-ichthyosis-premature ovarian failure syndrome", "shortest_name_length": 38}
{"curie": "UMLS:C0475319", "names": ["pelvic hematoma", "Pelvic hematoma", "pelvis; hematoma", "hematoma; pelvic", "Pelvic haematoma", "Pelvic hematoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pelvic hematoma", "shortest_name_length": 15}
{"curie": "UMLS:C0280175", "names": ["Stage IV Diffuse Large Cell Lymphoma", "Adult Diffuse Large Cell Lymphoma Stage IV", "stage IV adult diffuse large cell lymphoma", "Stage IV Adult Diffuse Large Cell Lymphoma", "adult diffuse large cell lymphoma, stage IV", "metastatic adult diffuse large cell lymphoma", "adult diffuse large cell lymphoma, metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Adult Diffuse Large Cell Lymphoma", "shortest_name_length": 36}
{"curie": "MONDO:0004657", "names": ["diffuse chorioretinitis", "diffuse retinochoroiditis", "Disseminated chorioretinitis", "disseminated chorioretinitis", "chorioretinitis; disseminated", "disseminated; chorioretinitis", "Disseminated retinochoroiditis", "retinochoroiditis; disseminated", "disseminated; retinochoroiditis", "Disseminated chorioretinitis NOS", "Disseminated chorioretinitis, NOS", "Disseminated retinochoroiditis NOS", "Disseminated chorioretinal inflammation", "Disseminated chorioretinitis (disorder)", "disseminated chorioretinitis (diagnosis)", "Disseminated chorioretinitis, unspecified", "Disseminated chorioretinitis and disseminated retinochoroiditis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disseminated chorioretinitis", "shortest_name_length": 23}
{"curie": "MONDO:0008832", "names": ["RAI", "POLYASPLENIA", "Polyasplenia", "Right isomerism", "right isomerism", "RIGHT ISOMERISM", "IVEMARK SYNDROME", "ivemark syndrome", "Ivemark syndrome", "Asplenia complex", "Ivemark Syndrome", "Asplenia syndrome", "asplenia syndrome", "Asplenia Syndrome", "Syndrome, Ivemark", "Ivemark's syndrome", "Asplenia Syndromes", "Syndrome, Asplenia", "Syndromes, Asplenia", "Polysplenia Syndrome", "Polysplenia syndrome", "polysplenia syndrome", "POLYSPLENIA SYNDROME", "Syndrome, Polysplenia", "Right-sided isomerism", "Polysplenia Syndromes", "right atrial isomerism", "Syndromes, Polysplenia", "Vah, autosomal recessive", "VAH, AUTOSOMAL RECESSIVE", "Bilateral left-sidedness", "splenic agenesis syndrome", "SPLENIC AGENESIS SYNDROME", "Splenic agenesis syndrome", "Situs Ambiguus with Asplenia", "Isomerism of right appendage", "Situs Ambiguus with Polysplenia", "right atrial isomerism (disease)", "right atrial isomerism (ivemark)", "Bilateral left-sidedness sequence", "bilateral right-sidedness sequence", "RAI - right sided atrial isomerism", "Bilateral right-sidedness sequence", "Isomerism of right atrial appendage", "Right Atrial Isomerism with Asplenia", "Congenital absence of spleen syndrome", "asplenia with cardiovascular anomalies", "Left Atrial Isomerism with Polysplenia", "Asplenia with Cardiovascular Anomalies", "ASPLENIA WITH CARDIOVASCULAR ANOMALIES", "Asplenia with Cardiovascular Abnormalities", "Bilateral left-sidedness sequence (disorder)", "Heterotaxy, Visceroatrial, Autosomal Recessive", "HETEROTAXY, VISCEROATRIAL, AUTOSOMAL RECESSIVE", "heterotaxy, Visceroatrial, autosomal recessive", "Isomerism of right atrial appendage (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "right atrial isomerism", "shortest_name_length": 3}
{"curie": "MONDO:0021297", "names": ["nasopharynx cancer, stage 0", "Nasopharyngeal cancer stage 0", "nasopharynx in situ carcinoma", "Stage 0 Nasopharynx Carcinoma", "stage 0 nasopharyngeal cancer", "nasopharynx carcinoma in situ", "stage 0 nasopharynx carcinoma", "Stage 0 Nasopharyngeal Cancer", "nasopharyngeal cancer, stage 0", "Carcinoma in situ of epipharynx", "nasopharyngeal carcinoma in situ", "Carcinoma in situ of Nasopharynx", "stage 0 carcinoma of nasopharynx", "Stage 0 Carcinoma of Nasopharynx", "Stage 0 Nasopharyngeal Carcinoma", "Nasopharyngeal Carcinoma in situ", "Carcinoma in situ of nasopharynx", "carcinoma in situ of nasopharynx", "stage 0 nasopharyngeal carcinoma", "stage 0 nasopharyngeal throat cancer", "Stage 0 Carcinoma of the Nasopharynx", "Carcinoma in situ of the Nasopharynx", "carcinoma in situ of the nasopharynx", "Carcinoma in situ of postnasal space", "Stage 0 Nasopharyngeal Throat Cancer", "stage 0 carcinoma of the nasopharynx", "Carcinoma in situ of nasopharynx, NOS", "Stage 0 Nasopharyngeal Carcinoma AJCC v8", "stage 0 nasopharyngeal carcinoma in situ", "Stage 0 Nasopharyngeal Carcinoma AJCC v7", "Stage 0 Nasopharyngeal Carcinoma AJCC v6", "stage 0 nasopharyngeal carcinoma aJCC v7", "stage 0 nasopharyngeal carcinoma aJCC v6", "Carcinoma in situ of nasopharyngeal wall", "stage 0 nasopharyngeal carcinoma aJCC v8", "PNS - carcinoma in situ of postnasal space", "Carcinoma in situ of nasopharynx (disorder)", "carcinoma in situ of nasopharynx (diagnosis)", "Carcinoma in situ of nasopharyngeal wall, NOS", "Stage 0 Nasopharyngeal Carcinoma AJCC v6, v7, and v8", "stage 0 nasopharyngeal carcinoma aJCC v6, v7, and v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma in situ of nasopharynx", "shortest_name_length": 27}
{"curie": "UMLS:C0854199", "names": ["CMML in Remission", "CMML in remission", "Chronic Myelomonocytic Leukemia in Remission", "chronic myelomonocytic leukemia in remission", "Chronic myelomonocytic leukemia, in remission", "Chronic myelomonocytic leukemia (in remission)", "Chronic Myelomonocytic Leukaemia (in Remission)", "Chronic myelomonocytic leukaemia (in remission)", "Chronic Myelomonocytic Leukemia (CMML) in Remission", "chronic myelomonocytic leukemia in remission (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic myelomonocytic leukemia (in remission)", "shortest_name_length": 17}
{"curie": "UMLS:C5555667", "names": ["GCRO", "Giant Cell-Rich Osteosarcoma", "Giant Cell Rich Osteosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Giant Cell-Rich Osteosarcoma", "shortest_name_length": 4}
{"curie": "UMLS:C3899278", "names": ["Early Rheumatoid Arthritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Early Rheumatoid Arthritis", "shortest_name_length": 26}
{"curie": "MONDO:0018094", "names": ["Waardenburg", "Mende syndrome", "syndrome waardenburg", "Waardenburg syndrome", "Waardenburg Syndrome", "waardenburg syndrome", "Syndrome, Waardenburg", "Waardenburgs Syndrome", "waardenburgs syndrome", "waardenburg's syndrome", "Waardenburg's syndrome", "Waardenburg's Syndrome", "Syndrome, Waardenburg's", "White forelock syndrome", "Waardenburg Shah syndrome", "Waardenburg, types I and II", "Waardenburg, types I and/or II", "Waardenburg syndrome (disorder)", "Waardenburg syndrome (diagnosis)", "van der Hoeve Halbertsona Waardenburg syndrome", "Van der Hoeve Halbertsma Waardenburg Gualdi syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Waardenburg syndrome", "shortest_name_length": 11}
{"curie": "UMLS:C4551544", "names": ["Stage II", "Stage II Cancer of Testis", "stage II testicular cancer", "Stage II Testicular Cancer", "Stage II Cancer of the Testis", "Stage II Testicular Cancer AJCC v7", "Stage II Testicular Cancer AJCC v6", "Stage II Testicular Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Testicular Cancer AJCC v6 and v7", "shortest_name_length": 8}
{"curie": "MONDO:0017868", "names": ["diencephalic-mesencephalic junction dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diencephalic-mesencephalic junction dysplasia", "shortest_name_length": 45}
{"curie": "MONDO:0009477", "names": ["STROMS", "CILD31", "Stromme syndrome", "Stromme Syndrome", "STROMME SYNDROME", "CILD31, FORMERLY", "stromme syndrome", "Stromme syndrome (disorder)", "primary ciliary dyskinesia 31", "ciliary dyskinesia, primary, 31", "ciliary dyskinesia, primary, type 31", "ciliary dyskinesia, primary, 31, formerly", "CILIARY DYSKINESIA, PRIMARY, 31, FORMERLY", "JEJUNAL ATRESIA WITH MICROCEPHALY AND OCULAR ANOMALIES", "Jejunal atresia-microcephaly-ocular anomalies syndrome", "jejunal atresia with microcephaly and ocular anomalies", "jejunal atresia-microcephaly-ocular anomalies syndrome", "Jejunal Atresia with Microcephaly and Ocular Anomalies", "Jejunal atresia, microcephaly, ocular anomalies syndrome", "apple peel syndrome with microcephaly and ocular anomalies", "APPLE PEEL SYNDROME WITH MICROCEPHALY AND OCULAR ANOMALIES", "Apple Peel Syndrome with Microcephaly and Ocular Anomalies", "apple-peel intestinal atresia-ocular anomalies-microcephaly syndrome", "Apple-peel intestinal atresia-ocular anomalies-microcephaly syndrome", "Apple peel intestinal atresia, ocular anomalies, microcephaly syndrome", "lethal fetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stromme syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0010310", "names": ["OSCS", "Robinow-Unger syndrome", "Osteopathia striata cranial sclerosis", "osteopathia striata cranial sclerosis", "osteopathia striata - cranial sclerosis", "HYPEROSTOSIS GENERALISATA WITH STRIATIONS", "hyperostosis generalisata with striations", "Hyperostosis Generalisata with Striations", "Hyperostosis generalisata with striations", "osteopathia striata with cranial sclerosis", "Osteopathia striata with cranial sclerosis", "OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS", "Osteopathia Striata with Cranial Sclerosis", "osteopathia striata-cranial sclerosis syndrome", "Osteopathia striata-cranial sclerosis syndrome", "Osteopathia striata with cranial sclerosis (disorder)", "Osteopathia striata with cranial sclerosis, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteopathia striata with cranial sclerosis", "shortest_name_length": 4}
{"curie": "MONDO:0016931", "names": ["Duplication of chromosome 10", "partial trisomy of chromosome 10", "Partial trisomy of chromosome 10", "partial duplication of chromosome 10", "Partial duplication of chromosome 10", "Partial trisomy of chromosome 10 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of chromosome 10", "shortest_name_length": 28}
{"curie": "UMLS:C4053908", "names": ["Type A Tylosis", "Late Onset Tylosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Type A Tylosis", "shortest_name_length": 14}
{"curie": "MONDO:0019910", "names": ["UPD(2)mat", "maternal uniparental disomy chromosome 2", "maternal uniparental disomy of chromosome 2", "Maternal uniparental disomy of chromosome 2", "maternal uniparental disomy of chromosome type 2", "Maternal uniparental disomy of chromosome 2 (disorder)", "Maternal uniparental disomy of chromosome 2 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maternal uniparental disomy of chromosome 2", "shortest_name_length": 9}
{"curie": "MONDO:0044201", "names": ["T+B+ SCID", "T-cell positive B-cell positive SCID", "T+ B+ severe combined immunodeficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T+ B+ severe combined immunodeficiency", "shortest_name_length": 9}
{"curie": "UMLS:C0152486", "names": ["salmonella sepsis", "Salmonella sepsis", "sepsis; Salmonella", "Salmonella; sepsis", "Salmonella septicemia", "Salmonella Septicemia", "salmonella septicemia", "SALMONELLA SEPTICEMIA", "Septicemia salmonella", "Salmonella septicaemia", "Septicaemia salmonella", "salmonella septicaemia", "Salmonella septicemia (diagnosis)", "infection; Salmonella, with sepsis", "Salmonella; infection, with sepsis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Salmonella sepsis", "shortest_name_length": 17}
{"curie": "MONDO:0013277", "names": ["DEE5", "EIEE5", "early infantile epileptic encephalopathy 5", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 5", "epileptic encephalopathy, early infantile, 5", "developmental and epileptic encephalopathy 5", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5", "developmental and epileptic encephalopathy, 5", "SPTAN1 early infantile epileptic encephalopathy", "epileptic encephalopathy, early infantile, type 5", "early infantile epileptic encephalopathy caused by mutation in SPTAN1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 5", "shortest_name_length": 4}
{"curie": "UMLS:C3274141", "names": ["Small Intestinal G Cell NET", "Small Intestinal Gastrinoma", "Small Intestinal Gastrin-Producing NET", "Small Intestinal Gastrin-Producing Neuroendocrine Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Intestinal Gastrin-Producing Neuroendocrine Tumor", "shortest_name_length": 27}
{"curie": "MONDO:0004039", "names": ["Bile duct papillary adenocarcinoma", "papillary extrahepatic bile duct adenocarcinoma", "papillary adenocarcinoma of extrahepatic bile duct", "papillary adenocarcinoma of extrahepatic bile duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papillary extrahepatic bile duct adenocarcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0013534", "names": ["HALP2", "HYPERALPHALIPOPROTEINEMIA 2", "hyperalphalipoproteinemia 2", "apolipoprotein c-III deficiency", "apolipoprotein C-III deficiency", "APOLIPOPROTEIN C-III DEFICIENCY", "Apolipoprotein C-III Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "apolipoprotein c-III deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0011834", "names": ["SMNA", "SCA18", "Spinocerebellar ataxia 18", "SPINOCEREBELLAR ATAXIA 18", "spinocerebellar ataxia 18", "Spinocerebellar ataxia type 18", "spinocerebellar ataxia type 18", "Spinocerebellar ataxia type 18 (disorder)", "sensorimotor neuropathy with ataxia autosomal dominant", "Sensorimotor neuropathy with ataxia, autosomal dominant", "SENSORIMOTOR NEUROPATHY WITH ATAXIA, AUTOSOMAL DOMINANT", "sensorimotor neuropathy with ataxia, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia type 18", "shortest_name_length": 4}
{"curie": "UMLS:C4521723", "names": ["Stage 0 Esophageal Squamous Cell Cancer", "Clinical Stage 0 Esophageal Squamous Cell Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage 0 Esophageal Squamous Cell Carcinoma AJCC v8", "shortest_name_length": 39}
{"curie": "MONDO:0020572", "names": ["CRPS II", "Causalgia", "causalgia", "CRPS Type II", "crps type ii", "Causalgia NOS", "CAUSALGIA SYNDROME", "Causalgia Syndrome", "causalgia syndrome", "Causalgia Syndromes", "causalgia; syndrome", "Syndrome, Causalgia", "syndrome; causalgia", "Deafferentation Pain", "Deafferentation pain", "Syndromes, Causalgia", "Pain, Deafferentation", "WEIR MITCHELL CAUSALGIA", "ERYTHROMELALGIA, TRAUMATIC", "Complex regional pain syndrome II", "Complex Regional Pain Syndrome II", "Complex regional pain syndrome type 2", "complex regional pain syndrome type 2", "Complex regional pain syndrome type II", "Complex Regional Pain Syndrome Type II", "Type II Complex Regional Pain Syndrome", "Complex regional pain syndrome Type II", "Complex regional pain syndrome, type II", "CRPS - Complex regional pain syndrome type II", "Complex regional pain syndrome, type II (disorder)", "Complex regional pain syndrome type II (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complex regional pain syndrome type 2", "shortest_name_length": 7}
{"curie": "MONDO:0004478", "names": ["CLL/SLL with unmutated IGVH", "CLL/SLL with Unmutated IGVH", "Pregerminal Center Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma", "pregerminal center chronic lymphocytic leukemia/small lymphocytic lymphoma", "chronic lymphocytic leukemia/small lymphocytic lymphoma with unmutated Immunoglobulin heavy chain variable-region Gene", "Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma with Unmutated Immunoglobulin Heavy Chain Variable-Region Gene"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pregerminal center chronic lymphocytic leukemia/small lymphocytic lymphoma", "shortest_name_length": 27}
{"curie": "UMLS:C5418892", "names": ["Metastatic Ovarian Clear Cell Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Ovarian Clear Cell Adenocarcinoma", "shortest_name_length": 44}
{"curie": "MONDO:0011789", "names": ["meningioma", "familial meningioma", "hereditary meningioma", "meningioma, SIS-related", "hereditary meningioma (disease)", "meningioma, NF2-related, somatic", "susceptibility to familial meningioma", "meningioma, familial, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial meningioma", "shortest_name_length": 10}
{"curie": "UMLS:C4526610", "names": ["Stage IIIA Thymoma", "Stage IIIA Thymoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Thymoma AJCC v8", "shortest_name_length": 18}
{"curie": "UMLS:C0264009", "names": ["Osteodystrophy", "osteodystrophy", "osteodystrophies", "Osteodystrophy NOS", "Osteodystrophy, NOS", "Osteodystrophy (disorder)", "osteodystrophy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Osteodystrophy", "shortest_name_length": 14}
{"curie": "UMLS:C1334772", "names": ["Minor Salivary Gland Carcinoma ex Pleomorphic Adenoma", "Carcinoma ex Pleomorphic Adenoma of Minor Salivary Gland", "Carcinoma ex Pleomorphic Adenoma of the Minor Salivary Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Minor Salivary Gland Carcinoma ex Pleomorphic Adenoma", "shortest_name_length": 53}
{"curie": "UMLS:C0553737", "names": ["CERVICAL DISCHARGE", "Cervical discharge", "cervical discharge", "Discharge uterine cervix", "DISCHARGE UTERINE CERVIX", "Pathologic Cervical Discharge"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Cervical Discharge", "shortest_name_length": 18}
{"curie": "MONDO:0010799", "names": ["Streptomycin Ototoxicity", "Streptomycin ototoxicity", "streptomycin ototoxicity", "STREPTOMYCIN OTOTOXICITY", "streptomycin-induced deafness", "DEAFNESS, STREPTOMYCIN-INDUCED", "Deafness, Streptomycin-Induced", "deafness, streptomycin-induced", "aminoglycoside-induced deafness", "DEAFNESS, AMINOGLYCOSIDE-INDUCED", "Deafness, Aminoglycoside-Induced", "deafness, aminoglycoside-induced", "aminoglycoside-induced hearing loss", "deafness, mitochondrial, modifier of, mitochondrial", "mitochondrial isolated neurosensory deafness with susceptibility to aminoglycoside exposure", "mitochondrial isolated sensorineural deafness with susceptibility to aminoglycoside exposure", "mitochondrial isolated neurosensory hearing loss with susceptibility to aminoglycoside exposure", "mitochondrial isolated sensorineural hearing loss with susceptibility to aminoglycoside exposure", "mitochondrial non-syndromic neurosensory deafness with susceptibility to aminoglycoside exposure", "mitochondrial non-syndromic sensorineural deafness with susceptibility to aminoglycoside exposure", "mitochondrial non-syndromic neurosensory hearing loss with susceptibility to aminoglycoside exposure", "mitochondrial non-syndromic sensorineural hearing loss with susceptibility to aminoglycoside exposure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness, aminoglycoside-induced", "shortest_name_length": 24}
{"curie": "UMLS:C0263454", "names": ["Chloracne", "CHLORACNE", "chloracne", "Chloracnes", "Chlorine acne", "Chlorine Acne", "Acne, Chlorine", "Chlorine Acnes", "Acnes, Chlorine", "chloracne (diagnosis)", "Chlorine acne (disorder)", "chloracne (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chloracne", "shortest_name_length": 9}
{"curie": "MONDO:0004520", "names": ["Intratubular Non-Seminoma", "intratubular embryonal carcinoma", "Intratubular Embryonal Carcinoma", "Stage 0 Testicular Embryonal Carcinoma", "stage 0 testicular embryonal carcinoma", "stage 0 testicular embryonal carcinoma aJCC v7", "stage 0 testicular embryonal carcinoma aJCC v6", "stage 0 testicular embryonal carcinoma aJCC v6 and v7", "Stage 0 Testicular Embryonal Carcinoma AJCC v6, v7, and v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intratubular embryonal carcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0007489", "names": ["TREVOR DISEASE", "Trevor disease", "Trevor's disease", "dysplasia epiphysealis hemimelica", "DYSPLASIA EPIPHYSEALIS HEMIMELICA", "Dysplasia epiphysealis hemimelica", "Dysplasia epiphysealis hemimelica (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dysplasia epiphysealis hemimelica", "shortest_name_length": 14}
{"curie": "MONDO:0009669", "names": ["SMA1", "SMA I", "SMA-I", "SMA type 1", "SMA type I", "Werdnig-Hoffmann", "werdnig hoffman disease", "WERDNIG-HOFFMAN DISEASE", "Werdnig-Hoffman disease", "Werdnig Hoffman Disease", "werdnig-hoffman disease", "Werdnig-Hoffmann Disease", "WERDNIG-HOFFMANN DISEASE", "WERDNIG HOFFMANN DISEASE", "werdnig-hoffmann disease", "werdnig hoffmann disease", "disease werdnig hoffmans", "Werdnig Hoffmann disease", "Werdnig-Hoffmann disease", "Werdnig Hoffmann Disease", "Spinal Muscular Atrophy 1", "SMA, INFANTILE ACUTE FORM", "Spinal muscular atrophy 1", "spinal muscular atrophy-1", "spinal muscular atrophy 1", "SMA, infantile acute form", "SMA, Infantile Acute Form", "Infantile Muscular Atrophy", "infantile muscular atrophy", "MUSCULAR ATROPHY, INFANTILE", "Muscular Atrophy, Infantile", "muscular atrophy, infantile", "type i spinal muscular atrophy", "Type I Spinal Muscular Atrophy", "WHD - Werdnig-Hoffmann disease", "Spinal muscular atrophy type I", "Spinal Muscular Atrophy Type I", "Spinal Muscular Atrophy, Type I", "Spinal muscular atrophy, type I", "SPINAL MUSCULAR ATROPHY, TYPE I", "spinal muscular atrophy, type I", "spinal muscular atrophy, type 1", "Muscular Atrophy, Spinal, Type I", "Infantile Spinal Muscular Atrophy", "infantile spinal muscular atrophy", "Infantile spinal muscular atrophy", "INFANTILE SPINAL MUSCULAR ATROPHY", "Spinal muscular atrophy, infantile", "Spinal Muscular Atrophy, Infantile", "Werdnig-Hoffmann disease (disorder)", "Muscular Atrophy, Spinal, Infantile", "infantile muscular atrophy (diagnosis)", "spinal muscular atrophies of childhood", "proximal spinal muscular atrophy type 1", "Proximal spinal muscular atrophy type 1", "progressive muscular atrophy of infancy", "Progressive muscular atrophy of infancy", "Spinal muscular atrophy infantile onset", "Infantile-onset spinal muscular atrophy", "Severe Infantile Spinal Muscular Atrophy", "proximal spinal muscular atrophy, type 1", "severe infantile spinal muscular atrophy", "Proximal Hereditary Motor Neuropathy Type I", "hereditary motor neuropathy proximal type I", "survival motor neuron spinal muscular atrophy", "HMN (Hereditary Motor Neuropathy) Proximal Type I", "HMN (Hereditary motor Neuropathy) Proximal type I", "HMN (hereditary motor neuropathy) proximal type I", "infantile spinal muscular atrophy, type 1 (Werdnig-Hoffman)", "Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]", "muscle; atrophy, spinal, infantile, type I (Werdnig-Hoffmann)", "atrophy; muscle, spinal, infantile, type I (Werdnig-Hoffmann)", "infantile spinal muscular atrophy, type 1 (Werdnig-Hoffman) (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal muscular atrophy, type 1", "shortest_name_length": 4}
{"curie": "UMLS:C4289580", "names": ["E-GB", "e-GB", "e-GBM", "E-GBM", "Epithelioid Glioblastoma", "Epithelioid glioblastoma", "Epithelioid glioblastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epithelioid glioblastoma", "shortest_name_length": 4}
{"curie": "MONDO:0008679", "names": ["WT1", "Wilms' tumor", "Wilms tumor 1", "nephroblastoma", "renal Wilms tumor", "Wilms tumor type 1", "Wilms tumor, somatic", "Wilms tumor, autosomal dominant, somatic mutation", "Wilms tumor, type 1, autosomal dominant, somatic mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wilms tumor 1", "shortest_name_length": 3}
{"curie": "MONDO:0009745", "names": ["CLN5", "VLINCL", "CLN5 disease", "Finnish Vlincl", "FINNISH vLINCL", "Finnish VLINCL", "CLN5 disease, adult", "CLN5 disease, juvenile", "neuronal ceroid lipofuscinosis 5", "Ceroid lipofuscinosis, neuronal 5", "Neuronal ceroid lipofuscinosis, 5", "ceroid lipofuscinosis, neuronal, 5", "CEROID LIPOFUSCINOSIS, NEURONAL, 5", "CLN5 neuronal ceroid lipofuscinosis", "neuronal ceroid lipofuscinosis type 5", "CLN5 disease, late infantile (subtype)", "ceroid lipofuscinosis, neuronal, type 5", "neuronal ceroid lipofuscinosis Finnish variant", "neuronal ceroid lipofuscinosis 5 variable age of onset", "Ceroid Lipofuscinosis, Neuronal, 5, Variable Age At Onset", "neuronal ceroid lipofuscinosis caused by mutation in CLN5", "CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSET", "ceroid lipofuscinosis, neuronal, 5, variable Age at onset", "neuronal ceroid lipofuscinosis, late infantile, Finnish variant", "NEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT", "Neuronal ceroid lipofuscinosis, Finnish variant, late infantile"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuronal ceroid lipofuscinosis 5", "shortest_name_length": 4}
{"curie": "UMLS:C1321861", "names": ["Carcinoma in a polyp", "Carcinoma in a Polyp", "Carcinoma in a polyp, NOS", "Adenocarcinoma in a polyp", "Adenocarcinoma in a polyp, NOS", "Carcinoma in adenomatous polyp", "Adenocarcinoma in tubular adenoma", "Adenocarcinoma in Tubular Adenoma", "Adenocarcinoma in polypoid adenoma", "Adenocarcinoma in Adenomatous Polyp", "Adenocarcinoma in adenomatous polyp", "adenocarcinoma in adenomatous polyp", "Adenocarcinoma in adenomatous polyp (disorder)", "adenocarcinoma in adenomatous polyp (diagnosis)", "Adenocarcinoma in adenomatous polyp (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma in adenomatous polyp", "shortest_name_length": 20}
{"curie": "MONDO:0035499", "names": ["CELSR1-related late-onset primary lymphedema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CELSR1-related late-onset primary lymphedema", "shortest_name_length": 44}
{"curie": "UMLS:C4526712", "names": ["Stage 0 Lung Cancer", "Stage 0 Lung Cancer AJCC v8", "Stage 0 Lung Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Lung Cancer AJCC v8", "shortest_name_length": 19}
{"curie": "UMLS:C0751883", "names": ["Postsynaptic Congenital Myasthenic Syndrome", "Postsynaptic Congenital Myasthenic Syndromes", "Postsynaptic congenital myasthenic syndromes", "Congenital Myasthenic Syndromes, Postsynaptic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Myasthenic Syndromes, Postsynaptic", "shortest_name_length": 43}
{"curie": "MONDO:0001104", "names": ["diffuse toxic goiter", "toxic diffuse goiter", "diffuse toxic goitre", "Diffuse toxic goitre", "Toxic diffuse goitre", "Diffuse toxic goiter", "Toxic diffuse goiter", "GOITER, TOXIC, DIFFUSE", "Toxic diffuse thyroid goiter", "THYROID GOITER TOXIC DIFFUSE", "Toxic diffuse thyroid goitre", "Toxic diffuse goiter (disorder)", "Toxic primary thyroid hyperplasia", "Thyrotoxicosis with diffuse goitre", "Thyrotoxicosis with diffuse goiter", "Toxic diffuse goiter without mention of thyrotoxic crisis or storm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "toxic diffuse goiter", "shortest_name_length": 20}
{"curie": "UMLS:C4067209", "names": ["Recurrent Acute Biphenotypic Leukemia", "Acute Biphenotypic Leukemia in Relapse", "leukemia acute biphenotypic in relapse", "acute biphenotypic leukemia in relapse", "acute biphenotypic leukemia in relapse (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute biphenotypic leukemia in relapse", "shortest_name_length": 37}
{"curie": "UMLS:C4525352", "names": ["II", "Stage II Intrahepatic Cholangiocarcinoma AJCC v8", "Stage II Intrahepatic Bile Duct Cancer (Cholangiocarcinoma)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Intrahepatic Cholangiocarcinoma AJCC v8", "shortest_name_length": 2}
{"curie": "UMLS:C1720821", "names": ["Membranoproliferative Glomerulonephritis, Type III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Membranoproliferative Glomerulonephritis, Type III", "shortest_name_length": 50}
{"curie": "UMLS:C0858355", "names": ["cocaine addict", "addicts cocaine", "cocaine addicted", "addicted cocaine", "addicted to cocaine", "Addicted to cocaine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Addicted to cocaine", "shortest_name_length": 14}
{"curie": "MONDO:0021653", "names": ["focal mucinosis", "focal mucinoses", "Focal cutaneous mucinosis", "cutaneous focal mucinosis", "Focal cutaneous mucinosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous focal mucinosis", "shortest_name_length": 15}
{"curie": "UMLS:C5555081", "names": ["Central Chondrosarcoma, Grade 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Chondrosarcoma, Grade 3", "shortest_name_length": 31}
{"curie": "MONDO:0007083", "names": ["PPKCA1", "PPKCA Stevanovic type", "PPKCA, STEVANOVIC TYPE", "Ppkca, Stevanovic type", "PPK-CA, Stevanovic type", "palmoplantar keratoderma with congenital alopecia", "palmoplantar keratoderma and congenital alopecia 1", "PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 1", "keratoderma-hypotrichosis-leukonychia totalis syndrome", "KERATODERMA-HYPOTRICHOSIS-LEUKONYCHIA TOTALIS SYNDROME", "palmoplantar keratoderma and congenital alopecia type 1", "alopecia congenita with hyperkeratosis of the palms and soles", "Palmoplantar keratoderma and congenital alopecia Stevanovic type", "palmoplantar keratoderma and congenital alopecia, Stevanovic type", "Palmoplantar keratoderma and congenital alopecia, Stevanovic type", "autosomal dominant palmoplantar keratoderma and congenital alopecia", "Autosomal dominant palmoplantar keratoderma and congenital alopecia", "autosomal dominant palmoplantar hyperkeratosis and congenital alopecia", "Autosomal dominant palmoplantar hyperkeratosis and congenital alopecia", "Autosomal dominant palmoplantar keratoderma and congenital alopecia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant palmoplantar keratoderma and congenital alopecia", "shortest_name_length": 6}
{"curie": "UMLS:C1335918", "names": ["Sarcoma NCI Grade 3", "Sarcoma NCI Grade III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sarcoma NCI Grade 3", "shortest_name_length": 19}
{"curie": "MONDO:0015412", "names": ["median facial cleft", "Midline facial cleft", "Tessier number 0-14 and 30 facial cleft"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "median facial cleft", "shortest_name_length": 19}
{"curie": "MONDO:0008206", "names": ["Ouvrier Billson syndrome", "Ouvrier-Billson syndrome", "PAROXYSMAL TONIC UPGAZE, BENIGN CHILDHOOD, WITH ATAXIA", "paroxysmal tonic upgaze, benign childhood, with ataxia", "Paroxysmal Tonic Upgaze, Benign Childhood, With Ataxia", "benign paroxysmal tonic upgaze of childhood with ataxia", "Benign paroxysmal tonic upgaze of childhood with ataxia", "Benign paroxysmal tonic upgaze of childhood with ataxia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign paroxysmal tonic upgaze of childhood with ataxia", "shortest_name_length": 24}
{"curie": "MONDO:0001638", "names": ["Protein-deficiency anemia", "protein deficiency anemia", "Protein deficiency anemia", "protein-deficiency anemia", "protein deficiency anaemia", "Protein-deficiency anaemia", "anemia; protein deficiency", "anemia; deficiency protein", "Anaemia;protein deficiency", "Protein deficiency anaemia", "protein-deficiency anaemia", "deficiency; anemia, protein", "anemia; deficiency, protein", "Anemia related to kwashiorkor", "Anaemia related to kwashiorkor", "protein; deficiency with anemia", "anemia due to protein deficiency", "Anemia due to protein deficiency", "Anaemia due to protein deficiency", "protein-deficiency anemia (diagnosis)", "Anemia due to protein deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "protein-deficiency anemia", "shortest_name_length": 25}
{"curie": "MONDO:0044817", "names": ["Idiopathic nonfamilial dystonia", "idiopathic nonfamilial dystonia", "dystonia idiopathic nonfamilial", "Idiopathic non-familial dystonia", "non-Familial Idiopathic dystonia", "idiopathic non-familial dystonia", "Non-Familial Idiopathic Dystonia", "dystonia; idiopathic, nonfamilial", "acquired idiopathic torsion dystonia", "idiopathic nonfamilial dystonia (diagnosis)", "Idiopathic non-familial dystonia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired idiopathic torsion dystonia", "shortest_name_length": 31}
{"curie": "MONDO:0001920", "names": ["CSOM", "chronic purulent otitis media", "Chronic purulent otitis media", "Otitis media;suppurative;chron", "Chronic Suppurative Otitis Media", "chronic media otitis suppurative", "chronic suppurative otitis Media", "Otitis media suppurative chronic", "chronic suppurative otitis media", "Chronic suppurative otitis media", "suppurative otitis media, chronic", "OTITIS MEDIA, CHRONIC, SUPPURATIVE", "otitis; media, chronic, suppurative", "Otitis media suppurative chronic NOS", "Chronic suppurative otitis media NOS", "Chronic otitis media with perforation", "CSOM - Chronic suppurative otitis media", "Chronic purulent otitis media (disorder)", "Chronic secretory otitis media, purulent", "Unspecified chronic suppurative otitis media", "chronic suppurative otitis media (diagnosis)", "Chronic otitis media with effusion, purulent", "Chronic non-suppurative otitis media with effusion - purulent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic purulent otitis media", "shortest_name_length": 4}
{"curie": "UMLS:C1142256", "names": ["Cardiac Perforation", "Cardiac perforation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiac perforation", "shortest_name_length": 19}
{"curie": "UMLS:C1711326", "names": ["Small Intestinal Medullary Cancer", "Small Intestinal Medullary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Intestinal Medullary Carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0016582", "names": ["congenital mitral malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital mitral malformation", "shortest_name_length": 30}
{"curie": "MONDO:0024418", "names": ["muscular fibrosis multifocal obstructed vessels"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular fibrosis multifocal obstructed vessels", "shortest_name_length": 47}
{"curie": "MONDO:0001072", "names": ["preeclampsia mild", "mild preeclampsia", "mild pre-eclampsia", "Mild pre-eclampsia", "mild; pre-eclampsia", "Pre-eclamptic, mild", "pre-eclampsia; mild", "Mild pre-eclamptic toxemia", "Mild pre-eclamptic toxaemia", "mild preeclampsia (diagnosis)", "Mild pre-eclampsia (disorder)", "PET - Mild pre-eclamptic toxemia", "Mild or unspecified pre-eclampsia", "PET - Mild pre-eclamptic toxaemia", "Mild proteinuric hypertension of pregnancy", "Mild or unspecified pre-eclampsia, unspecified as to episode of care", "Mild or unspecified pre-eclampsia, unspecified as to episode of care or not applicable"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mild pre-eclampsia", "shortest_name_length": 17}
{"curie": "UMLS:C1336820", "names": ["Treatment-Induced Anemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Treatment-Induced Anemia", "shortest_name_length": 24}
{"curie": "UMLS:C5555152", "names": ["Bone Erdheim-Chester Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone Erdheim-Chester Disease", "shortest_name_length": 28}
{"curie": "UMLS:C5235850", "names": ["Refractory Small Cell Glioblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Small Cell Glioblastoma", "shortest_name_length": 34}
{"curie": "MONDO:0020674", "names": ["Vascular insufficiency", "VASCULAR INSUFFICIENCY", "vascular insufficiency", "insufficiency vascular", "insufficiency; vascular", "vascular; insufficiency", "Vascular insufficiency, NOS", "vascular insufficiency disorder", "Vascular insufficiency (disorder)", "vascular insufficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vascular insufficiency disorder", "shortest_name_length": 22}
{"curie": "MONDO:0008478", "names": ["Schmid metaphyseal dysostosis", "spondylometaphyseal dysplasia Schmidt type", "Spondylometaphyseal dysplasia Schmidt type", "Spondylometaphyseal Dysplasia, Schmidt Type", "spondylometaphyseal dysplasia, Schmidt type", "SPONDYLOMETAPHYSEAL DYSPLASIA, SCHMIDT TYPE", "Spondylometaphyseal dysplasia Algerian type", "Spondylometaphyseal dysplasia, Schmidt type", "spondylometaphyseal dysplasia Algerian type", "SPONDYLOMETAPHYSEAL DYSPLASIA, ALGERIAN TYPE", "Spondylometaphyseal dysplasia, Algerian type", "spondylometaphyseal dysplasia, Algerian type", "Spondylometaphyseal dysplasia Schmidt type (disorder)", "Spondylometaphyseal Dysplasia With Severe Genu Valgum", "Spondylometaphyseal dysplasia with severe genu valgum", "SPONDYLOMETAPHYSEAL DYSPLASIA WITH SEVERE GENU VALGUM", "spondylometaphyseal dysplasia with severe genu valgum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondylometaphyseal dysplasia, Schmidt type", "shortest_name_length": 29}
{"curie": "UMLS:C0265833", "names": ["Congenital pulmonary regurgitation", "pulmonary regurgitation congenital", "Congenital Pulmonary Insufficiency", "congenital pulmonary regurgitation", "Pulmonary regurgitation, congenital", "regurgitation; pulmonary, congenital", "pulmonary; regurgitation, congenital", "Congenital Pulmonary Valve Insufficiency", "Congenital pulmonary valve insufficiency", "pulmonary valve; insufficiency, congenital", "Congenital insufficiency of pulmonary valve", "pulmonary; insufficiency, valve, congenital", "Congenital Insufficiency of Pulmonary Valve", "insufficiency; pulmonary, valve, congenital", "congenital pulmonary regurgitation (diagnosis)", "Congenital insufficiency of the pulmonary valve", "Congenital insufficiency of pulmonary valve (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital insufficiency of pulmonary valve", "shortest_name_length": 34}
{"curie": "UMLS:C0751846", "names": ["stroke of left middle cerebral artery", "Left Middle Cerebral Artery Infarction", "stroke of left middle cerebral artery (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Left Middle Cerebral Artery Infarction", "shortest_name_length": 37}
{"curie": "UMLS:C5237217", "names": ["hATTR-CM", "Hereditary Transthyretin Amyloid Cardiomyopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hereditary Transthyretin Amyloid Cardiomyopathy", "shortest_name_length": 8}
{"curie": "MONDO:0010500", "names": ["MRXS33", "MENTAL RETARDATION, X-LINKED, SYNDROMIC 33", "mental retardation, X-linked, syndromic 33", "mental retardation, X-linked, syndromic type 33", "intellectual disability, X-linked, syndromic 33", "TAF1 X-linked syndromic intellectual disability", "intellectual disability, X-linked, syndromic type 33", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33", "X-linked syndromic intellectual disability caused by mutation in TAF1", "intellectual developmental disorder, X-linked syndromic 33, X-linked recessive", "X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome", "X-linked intellectual disability, global development delay, facial dysmorphism, sacral caudal remnant syndrome", "X-linked intellectual disability, global development delay, facial dysmorphism, sacral caudal remnant syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked, syndromic 33", "shortest_name_length": 6}
{"curie": "UMLS:C0750815", "names": ["nhl colon", "Colon Non-Hodgkin Lymphoma", "Colon NonHodgkin's Lymphoma", "Colon Non-Hodgkin's Lymphoma", "lymphoma, nonhodgkins, colon", "Colonic NonHodgkin's Lymphoma", "Non-hodgkin lymphoma of colon", "Colonic Non-Hodgkin's Lymphoma", "lymphoma, non-hodgkin's, colon", "Non-Hodgkin's Lymphoma of Colon", "Non-Hodgkin's Lymphoma of the Colon", "Primary Colon Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-hodgkin lymphoma of colon", "shortest_name_length": 9}
{"curie": "UMLS:C3489628", "names": ["Autosomal Dominant Thrombocytoses", "Autosomal Dominant Thrombocytosis", "Thrombocytoses, Autosomal Dominant", "Dominant Thrombocytoses, Autosomal", "Dominant Thrombocytosis, Autosomal", "Thrombocytosis, Autosomal Dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thrombocytosis, Autosomal Dominant", "shortest_name_length": 33}
{"curie": "MONDO:0001685", "names": ["Chronic follicular conjunctivitis", "chronic follicular conjunctivitis", "Chronic follicular conjunctivitis (disorder)", "chronic follicular conjunctivitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic follicular conjunctivitis", "shortest_name_length": 33}
{"curie": "MONDO:0008777", "names": ["GDLD", "GDCD", "Cdgdl", "CDGDL", "Amyloid of cornea", "amyloidosis corneal", "Corneal amyloidosis", "corneal amyloidosis", "amyloidosis, corneal", "AMYLOIDOSIS, CORNEAL", "Amyloidosis, corneal", "Lattice corneal dystrophy type3", "lattice corneal dystrophy type 3", "Corneal dystrophy, Lattice type 3", "lattice corneal dystrophy, type 3", "corneal dystrophy, lattice type 3", "Lattice corneal dystrophy type III", "CORNEAL DYSTROPHY, LATTICE TYPE III", "Lattice Corneal Dystrophy, Type III", "Corneal Dystrophy, Lattice Type III", "lattice corneal dystrophy, type III", "LATTICE CORNEAL DYSTROPHY, TYPE III", "corneal dystrophy gelatinous droplike", "Gelatinous droplike corneal dystrophy", "GELATINOUS DROP-LIKE CORNEAL DYSTROPHY", "gelatinous drop-like corneal dystrophy", "Gelatinous Drop-Like Corneal Dystrophy", "Gelatinous drop-like corneal dystrophy", "subepithelial amyloidosis of the cornea", "Corneal dystrophy, gelatinous drop-like", "CORNEAL DYSTROPHY, GELATINOUS DROP-LIKE", "corneal dystrophy, gelatinous drop-like", "Subepithelial amyloidosis of the cornea", "amyloid corneal dystrophy, Japanese type", "AMYLOID CORNEAL DYSTROPHY, JAPANESE TYPE", "Amyloid corneal dystrophy, Japanese type", "Primary familial amyloidosis of the cornea", "primary familial amyloidosis of the cornea", "lattice corneal dystrophy, type III (diagnosis)", "Gelatinous droplike corneal dystrophy (disorder)", "Gelatinous droplike corneal dystrophy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gelatinous drop-like corneal dystrophy", "shortest_name_length": 4}
{"curie": "MONDO:0009565", "names": ["microcephaly glomerulonephritis Marfanoid habitus", "MARFANOID HABITUS WITH MICROCEPHALY AND GLOMERULONEPHRITIS", "MARFANOID habitus with microcephaly and glomerulonephritis", "Microcephaly-glomerulonephritis-marfanoid habitus syndrome", "microcephaly-glomerulonephritis-marfanoid habitus syndrome", "marfanoid habitus-microcephaly-glomerulonephritis syndrome", "Marfanoid Habitus with Microcephaly and Glomerulonephritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly-glomerulonephritis-marfanoid habitus syndrome", "shortest_name_length": 49}
{"curie": "MONDO:0009707", "names": ["myopathy with giant abnormal mitochondria", "MYOPATHY WITH GIANT ABNORMAL MITOCHONDRIA", "Myopathy with Giant Abnormal Mitochondria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy with giant abnormal mitochondria", "shortest_name_length": 41}
{"curie": "MONDO:0002814", "names": ["adrenal carcinoma", "adrenal gland carcinoma", "carcinoma of adrenal gland", "carcinoma of the adrenal gland", "carcinoma of the Adrenal gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adrenal carcinoma", "shortest_name_length": 17}
{"curie": "UMLS:C1266003", "names": ["Papillary squamous cell carcinoma in situ", "Non-Invasive Papillary Squamous Cell Carcinoma", "Papillary squamous cell carcinoma, non-invasive", "Papillary squamous cell carcinoma, non-invasive (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Papillary squamous cell carcinoma, non-invasive", "shortest_name_length": 41}
{"curie": "MONDO:0012309", "names": ["PFM2", "PARIETAL FORAMINA 2", "Parietal Foramina 2", "parietal foramina 2", "ALX4 parietal foramina", "parietal foramina type 2", "parietal foramina caused by mutation in ALX4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parietal foramina 2", "shortest_name_length": 4}
{"curie": "MONDO:0036212", "names": ["CSPSD", "Fatty acyl-CoA reductase 1 superactivity", "CATARACTS, SPASTIC PARAPARESIS, AND SPEECH DELAY", "spastic paraparesis-cataracts-speech delay syndrome", "Spastic paraparesis-cataracts-speech delay syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic paraparesis-cataracts-speech delay syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C1335046", "names": ["Non-Neoplastic Thymus Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Thymus Disorder", "shortest_name_length": 30}
{"curie": "MONDO:0000447", "names": ["PCLD", "ADPLD", "polycystic; liver", "liver; polycystic", "cystic liver disease", "cystic disease liver", "cystic diseases liver", "Congenital cystic liver", "cystic disease of liver", "congenital hepatic cyst", "Cystic disease of liver", "of liver cystic disease", "Congenital hepatic cyst", "liver polycystic disease", "Polycystic Liver Disease", "Polycystic liver disease", "disease liver polycystic", "POLYCYSTIC LIVER DISEASE", "polycystic liver disease", "fibrocystic liver disease", "Fibrocystic liver disease", "diseases liver polycystic", "polycystic; disease, liver", "AD polycystic liver disease", "Fibrocystic disease of liver", "PLD - Polycystic liver disease", "congenital cystic liver disease", "isolated polycystic liver disease", "Isolated polycystic liver disease", "Congenital cystic disease of liver", "Congenital polycystic liver disease", "Congenital polycystic disease of liver", "liver; disease, polycystic (congenital)", "disease (or disorder); polycystic, liver", "autosomal dominant polycystic liver disease", "isolated congenital polycystic liver disease", "Congenital cystic disease of liver (disorder)", "Isolated autosomal dominant polycystic liver disease", "disease (or disorder); liver, polycystic (congenital)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant polycystic liver disease", "shortest_name_length": 4}
{"curie": "MONDO:0019620", "names": ["pouch; esophagus", "esophagus; pouch", "Esophageal pouch", "esophageal pouch", "Oesophageal pouch", "oesophageal pouch", "esophageal diverticula", "diverticulum esophagus", "Esophageal Diverticula", "ESOPHAGEAL DIVERTICULA", "Esophagus--Diverticula", "Diverticulum esophagus", "diverticula esophageal", "esophagus diverticulum", "Diverticulum esophageal", "Diverticulum oesophagus", "Esophageal diverticulum", "ESOPHAGEAL DIVERTICULUM", "Esophageal Diverticulum", "esophageal diverticulum", "Diverticula, Esophageal", "esophagus; diverticulum", "diverticulum; esophagus", "Diverticulum oesophageal", "Oesophageal diverticulum", "oesophageal diverticulum", "Diverticulum, Esophageal", "Diverticulum of esophagus", "diverticulum of esophagus", "Diverticulum of oesophagus", "congenital esophageal pouch", "Congenital esophageal pouch", "esophageal pouch (diagnosis)", "Congenital oesophageal pouch", "CONGENITAL ESOPHAGEAL DIVERTICULUM", "congenital esophageal diverticulum", "Congenital esophageal diverticulum", "Esophageal diverticulum (diagnosis)", "esophageal diverticulum (diagnosis)", "Congenital diverticulum of esophagus", "Diverticulum of esophagus (disorder)", "Congenital diverticulum of oesophagus", "diverticulum of esophagus (diagnosis)", "Congenital esophageal pouch (disorder)", "congenital esophageal diverticulum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital esophageal diverticulum", "shortest_name_length": 16}
{"curie": "MONDO:0054868", "names": ["Ileus meconium", "Meconium Ileus", "meconium ileus", "ileus meconium", "Meconium ileus", "MECONIUM ILEUS", "ILEUS, MECONIUM", "Ileus, Meconium", "Meconium ileus NOS", "Meconium obstruction", "Meconium ileus of newborn", "Meconium ileus (disorder)", "Meconium ileus equivalent", "Meconium ileus in neonates", "Meconium ileus of the newborn", "meconium ileus cystic fibrosis", "MIE - Meconium ileus equivalent", "Meconium ileus in cystic fibrosis", "Meconium ileus on ultrasonography", "Meconium ileus equivalent syndrome", "cystic fibrosis with meconium ileus", "Cystic Fibrosis with Meconium Ileus", "Cystic fibrosis with meconium ileus", "Distal intestinal obstruction syndrome", "meconium obstruction due to meconium ileus", "DIOS - Distal intestinal obstruction syndrome", "Cystic fibrosis with meconium ileus (disorder)", "cystic fibrosis with meconium ileus (diagnosis)", "Distal intestinal obstruction syndrome (disorder)", "Meconium obstruction of intestine in mucoviscidosis", "meconium obstruction due to meconium ileus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "meconium ileus", "shortest_name_length": 14}
{"curie": "UMLS:C5420435", "names": ["Maxillofacial Osteoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Maxillofacial Osteoma", "shortest_name_length": 21}
{"curie": "MONDO:0015675", "names": ["Worms NOS", "Distomiasis", "distomiasis", "Trematodosis", "Distomatosis", "trematodosis", "distomatosis", "trematodiasis", "Fluke disease", "Trematodiasis", "fluke disease", "Fluke infection", "fluke infection", "diseases flukes", "Distomiasis NOS", "infection; fluke", "fluke; infection", "flukes infection", "flukes infections", "Fluke disease NOS", "Fluke disease, NOS", "trematode infection", "Trematode infection", "Fluke infection NOS", "Trematode Infection", "Trematode infections", "Infection, Trematode", "Trematode Infections", "infection trematodes", "Trematode infestation", "Infections, Trematode", "Infection by Trematode", "Disease due to Trematoda", "Trematode infection, NOS", "DISEASES DUE TO TREMATODA", "Infection by Trematode, NOS", "Fluke infection, unspecified", "Trematode infection (disorder)", "trematode infection (diagnosis)", "Trematode infection, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distomatosis", "shortest_name_length": 9}
{"curie": "MONDO:0001480", "names": ["Cancer of undescended testis", "Malignant tumor of retained testis", "malignant tumor of retained testis", "Malignant tumour of retained testis", "malignant tumour of retained testis", "Malignant tumor of undescended testis", "malignant neoplasm of retained testis", "Malignant neoplasm of retained testis", "malignant tumor of undescended testis", "malignant tumour of undescended testis", "Malignant tumour of undescended testis", "Malignant neoplasm of undescended testis", "malignant neoplasm of undescended testis", "Malignant neoplasm of testis, undescended", "Malignant tumor of undescended testis (disorder)", "malignant neoplasm of retained testis (diagnosis)", "malignant neoplasm of undescended testis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant tumor of undescended testis", "shortest_name_length": 28}
{"curie": "MONDO:0014182", "names": ["DFNB88", "autosomal recessive deafness 88", "DEAFNESS, AUTOSOMAL RECESSIVE 88", "deafness, autosomal recessive 88", "deafness, autosomal recessive type 88", "autosomal recessive nonsyndromic deafness 88", "ELMOD3 autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 88", "autosomal recessive nonsyndromic deafness type 88", "autosomal recessive nonsyndromic deafness caused by mutation in ELMOD3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 88", "shortest_name_length": 6}
{"curie": "UMLS:C1335698", "names": ["Recurrent Childhood Optic Nerve Astrocytoma", "Recurrent Pediatric Optic Nerve Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Optic Nerve Astrocytoma", "shortest_name_length": 43}
{"curie": "MONDO:0006976", "names": ["somatostatinoma", "SOMATOSTATINOMA", "Somatostatinoma", "Somatostatinomas", "Delta cell tumor", "Delta Cell Tumor", "Delta cell tumour", "tumor of Delta cells", "Tumor of Delta Cells", "Somatostatinoma, NOS", "somatostatin cell tumor", "Somatostatin Cell Tumor", "Somatostatin cell tumor", "somatostatin cell tumour", "Somatostatin cell tumour", "tumor of the Delta cells", "Tumor of the Delta Cells", "ampullary somatostatinoma", "carcinoid somatostatinoma", "malignant islet cell tumor", "Somatostatin-Producing NET", "Somatostatinoma (disorder)", "somatostatin cell neoplasm", "somatostatin-producing NET", "Somatostatin cell neoplasm", "Somatostatin cell tumor, NOS", "Somatostatin Producing Tumor", "somatostatin-producing tumor", "Somatostatin-Producing Tumor", "somatostatin producing tumor", "Somatomedin-secreting carcinoid", "Somatostatinoma (morphologic abnormality)", "somatostatin-secreting pancreatic neoplasm", "somatostatin-producing neuroendocrine tumor", "Somatostatin-Producing Neuroendocrine Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "somatostatinoma", "shortest_name_length": 15}
{"curie": "UMLS:C3899654", "names": ["Laryngeal Throat Cancer", "Childhood Laryngeal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Laryngeal Carcinoma", "shortest_name_length": 23}
{"curie": "MONDO:0035592", "names": ["CIL-F", "facial infused lipomatosis", "fibroadipose infiltrating lipomatosis", "congenital infiltrating lipomatosis of the face"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital infiltrating lipomatosis of the face", "shortest_name_length": 5}
{"curie": "MONDO:0005083", "names": ["psoriasi", "psoriases", "Psoriases", "PSORIASIS", "Psoriasis", "psoriasis", "Psoriasis, NOS", "Psoriasiform eczema", "Psoriasis (disorder)", "psoriasis (diagnosis)", "Psoriasis, unspecified", "Psoriasiform Dermatitis", "DERMATITIS PSORIASIFORM", "psoriasiform dermatitis", "Dermatitis psoriasiform", "Psoriasiform dermatitis", "Psoriasiform eczema (disorder)", "Psoriasiform dermatitis (disorder)", "psoriasiform dermatitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "psoriasis", "shortest_name_length": 8}
{"curie": "MONDO:0100391", "names": ["AML, t(2;12)", "acute myeloid leukemia, t(2;12)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, t(2;12)", "shortest_name_length": 12}
{"curie": "MONDO:0016660", "names": ["MCPH", "true microcephaly", "microcephaly vera", "True Microcephaly", "Microcephaly vera", "True microcephaly", "microcephalia vera", "Microcephalia vera", "Microcephaly Primary Hereditary", "autosomal recessive primary microcephaly", "primary autosomal recessive microcephaly", "Autosomal Recessive Primary Microcephaly", "Primary Autosomal Recessive Microcephaly", "Autosomal recessive primary microcephaly", "microcephaly, primary autosomal recessive", "microcephaly, primary, autosomal recessive", "Autosomal recessive primary microcephaly (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive primary microcephaly", "shortest_name_length": 4}
{"curie": "MONDO:0010884", "names": ["Scapulohumeral muscular dystrophy", "muscular dystrophy, scapulohumeral", "MUSCULAR DYSTROPHY, SCAPULOHUMERAL", "Muscular Dystrophy, Scapulohumeral", "Scapulohumeral muscular dystrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy, scapulohumeral", "shortest_name_length": 33}
{"curie": "UMLS:C0856808", "names": ["Polymorphonuclear leucocytosis", "Polymorphonuclear leukocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Polymorphonuclear leucocytosis", "shortest_name_length": 30}
{"curie": "MONDO:0016527", "names": ["Ldh Deficiency", "LDH deficiency", "Lactate dehydrogenase deficiency", "Lactate Dehydrogenase Deficiency", "deficiency dehydrogenase lactate", "lactate dehydrogenase deficiency", "Deficiency of Lactate Dehydrogenase", "Lactic acid dehydrogenase deficiency", "Deficiency of L-lactate dehydrogenase", "LDH - Lactate dehydrogenase deficiency", "Deficiency of lactic acid dehydrogenase", "Lactate Dehydrogenase Subunit Deficiencies", "GSD due to lactate dehydrogenase deficiency", "Lactate dehydrogenase deficiency (disorder)", "Deficiency of L-lactate dehydrogenase (disorder)", "glycogenosis due to lactate dehydrogenase deficiency", "glycogen storage disease due to lactate dehydrogenase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease due to lactate dehydrogenase deficiency", "shortest_name_length": 14}
{"curie": "MONDO:0014977", "names": ["LGMD2Z", "LGMDR21", "LGMD type 2Z", "POGLUT1-related LGMD R21", "limb-girdle muscular dystrophy 21", "Limb girdle muscular dystrophy type 2Z", "limb-girdle muscular dystrophy type 2Z", "Limb-Girdle Muscular Dystrophy Type 2Z", "Limb-girdle muscular dystrophy type 2Z", "muscular dystrophy, limb-girdle, type 2Z", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Z", "POGLUT1-related limb girdle muscular dystrophy R21", "POGLUT1-related limb-girdle muscular dystrophy R21", "muscular dystrophy, limb-girdle, autosomal recessive 21", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 21", "POGLUT1 autosomal recessive limb-girdle muscular dystrophy", "autosomal recessive limb-girdle muscular dystrophy type 2Z", "Autosomal recessive limb girdle muscular dystrophy type 2Z", "Autosomal recessive limb-girdle muscular dystrophy type 2Z", "autosomal recessive limb-girdle muscular dystrophy type 2R1", "Protein O-glucosyltransferase 1-related limb girdle muscular dystrophy R21", "autosomal recessive limb-girdle muscular dystrophy caused by mutation in POGLUT1", "Protein O-glucosyltransferase 1-related limb girdle muscular dystrophy R21 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive limb-girdle muscular dystrophy type 2R1", "shortest_name_length": 6}
{"curie": "MONDO:0002605", "names": ["liver PEComa", "Liver PEComa", "liver angiomyolipoma", "Liver Angiomyolipoma", "hepatic angiomyolipoma", "Hepatic angiomyolipoma", "Hepatic Angiomyolipoma", "angiomyolipoma of liver", "Angiomyolipoma of liver", "Angiomyolipoma of liver (disorder)", "angiomyolipoma of liver (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatic angiomyolipoma", "shortest_name_length": 12}
{"curie": "UMLS:C0578735", "names": ["Axillary Adenopathy", "axillary adenopathy", "Axillary adenopathy", "axillary lymphadenopathy", "AXILLARY LYMPHADENOPATHY", "Axillary lymphadenopathy", "Lymphadenopathy axillary", "Axillary Lymphadenopathy", "enlarged axillary lymph node", "Axillary lymph nodes enlarged", "axillary lymph nodes enlarged", "AXILLARY LYMPH NODE ENLARGEMENT", "Enlargement of axillary lymph node", "Axillary lymphadenopathy (disorder)", "enlarged axillary lymph node (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Axillary lymphadenopathy", "shortest_name_length": 19}
{"curie": "MONDO:0016139", "names": ["qualitative or quantitative protein defects in neuromuscular diseases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative protein defects in neuromuscular diseases", "shortest_name_length": 69}
{"curie": "MONDO:0700184", "names": ["Feline Large Granular Lymphocyte Lymphoma", "feline large granular lymphocyte lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "feline large granular lymphocyte lymphoma", "shortest_name_length": 41}
{"curie": "MONDO:0024616", "names": ["MYRINGITIS", "Tympanitis", "tympanitis", "myringitis", "Myringitis", "Myringitis NOS", "Myringitis, NOS", "EARDRUM INFLAMMATION", "Myringitis (disorder)", "Unspecified myringitis", "myringitis (diagnosis)", "Inflammation;tympanic membra", "TYMPANIC MEMBRANE INFLAMMATION", "tympanic membrane inflammation", "Tympanic membrane inflammation", "inflammation of tympanic membrane", "inflammation of the tympanic membrane", "Unspecified myringitis, unspecified ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tympanitis", "shortest_name_length": 10}
{"curie": "MONDO:0010112", "names": ["symmetric infantile thalamic degeneration", "THALAMIC DEGENERATION, SYMMETRIC INFANTILE", "thalamic degeneration, symmetric infantile", "Thalamic Degeneration, Symmetric Infantile", "Thalamic degeneration symmetrical infantile", "Symmetrical infantile thalamic degeneration", "symmetrical thalamic degeneration in infants"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thalamic degeneration, symmetric infantile", "shortest_name_length": 41}
{"curie": "UMLS:C4288372", "names": ["Primary Peritoneal High-Grade Serous Adenocarcinoma", "Primary Peritoneal High Grade Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Peritoneal High Grade Serous Adenocarcinoma", "shortest_name_length": 51}
{"curie": "MONDO:0000291", "names": ["Acanthamoeba encephalitis", "granulomatous amebic encephalitis", "Granulomatous amebic encephalitis", "Granulomatous amoebic encephalitis", "granulomatous amoebic encephalitis", "Granulomatous amebic encephalomyelitis", "Granulomatous amoebic encephalomyelitis", "Acanthamoeba granulomatous encephalitis", "PAM - Primary amebic meningoencephalitis", "PAM - Primary amoebic meningoencephalitis", "Granulomatous amebic encephalitis (disorder)", "GAE - Granulomatous amebic encephalomyelitis", "GAE - Granulomatous amoebic encephalomyelitis", "granulomatous amebic encephalitis due to Acanthamoeba", "Granulomatous Amebic Encephalitis due to Acanthamoeba"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "granulomatous amebic encephalitis", "shortest_name_length": 25}
{"curie": "UMLS:C3272836", "names": ["Colorectal Perineurioma", "Colorectal Fibroblastic Polyp"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Perineurioma", "shortest_name_length": 23}
{"curie": "MONDO:0024270", "names": ["INTESTINAL PARASITE", "intestinal parasite", "intestinal parasites", "parasites intestinal", "Parasites;intestinal", "Intestinal parasitism", "intestinal parasitism", "intestinal; parasitism", "parasitism; intestinal", "intestinal; infestation", "infestation; intestinal", "GASTROINTESTINAL PARASITE", "gastrointestinal parasite", "parasite gastrointestinal", "Intestinal parasitism, NOS", "gastrointestinal parasites", "Parasitic Intestinal Disease", "parasitic intestinal disease", "intestine parasitic infection", "Intestinal Disease, Parasitic", "parasitic intestinal disorder", "parasitic intestinal diseases", "intestinal parasitic diseases", "Disease, Parasitic Intestinal", "disease, parasitic intestinal", "intestinal disease, parasitic", "Parasitic Intestinal Diseases", "Parasitic infection intestinal", "Intestinal Diseases, Parasitic", "Diseases, Parasitic Intestinal", "parasitic intestinal infection", "intestinal parasitic infection", "parasitic; disease, intestinal", "diseases, parasitic intestinal", "infections intestinal parasitic", "intestinal infections parasitic", "Intestinal parasitism (disorder)", "intestinal parasitism (diagnosis)", "Unspecified intestinal parasitism", "Intestinal parasitism, unspecified", "parasitic; infestation, intestinal", "parasitic gastrointestinal disorder", "parasitic intestinal infection (diagnosis)", "infestation; parasite, parasitic, intestinal", "disease (or disorder); parasitic, intestinal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parasitic intestinal disorder", "shortest_name_length": 19}
{"curie": "UMLS:C5204621", "names": ["Bladder Granular Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder Granular Cell Tumor", "shortest_name_length": 27}
{"curie": "UMLS:C3899349", "names": ["Disorder of AMH Receptor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disorder of AMH Receptor", "shortest_name_length": 24}
{"curie": "MONDO:0019391", "names": ["FA", "fanconi anemia", "FANCONI ANEMIA", "anemia fanconi", "Fanconi anemia", "Fanconi Anemia", "Fanconi Anemias", "fanconi anemias", "Fanconi; anemia", "anemia; Fanconi", "anemia fanconis", "Anemia, Fanconi", "Fanconi anaemia", "Fanconi's Anemia", "Fanconi's anemia", "fanconi syndrome", "FANCONI'S ANEMIA", "anemia fanconi's", "Anemias, Fanconi", "fanconi's anemia", "fanconis syndrome", "fanconi's anaemia", "Fanconi dysplasia", "Anemia, Fanconi's", "Fanconi's anaemia", "Fanconi Pancytopenia", "Fanconi pancytopenia", "Fanconi Panmyelopathy", "Fanconi panmyelopathy", "PANMYELOPATHY, FANCONI", "Panmyelopathy, Fanconi", "congenital pancytopenia", "PANCYTOPENIA, CONGENITAL", "pancytopenia; congenital", "pancytopenia, congenital", "Pancytopenia, Congenital", "congenital; pancytopenia", "Fanconi Hypoplastic Anemia", "congenital aplastic anemia", "Fanconi's anemia (disorder)", "Primary Erythroid Hypoplasia", "Fanconi's anemia (diagnosis)", "PRIMARY ERYTHROID HYPOPLASIA", "Fanconi's hypoplastic anemia", "primary erythroid hypoplasia", "Fanconi pancytopenia syndrome", "Fanconi's hypoplastic anaemia", "Pancytopenia-dysmelia syndrome", "constitutional aplastic anemia", "Fanconi's pancytopenia syndrome", "Fanconi's familial refractory anemia", "Fanconi's familial refractory anaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fanconi anemia", "shortest_name_length": 2}
{"curie": "MONDO:0002805", "names": ["hidradenoma", "Hidradenoma", "Acrospiroma", "acrospiroma", "Syringoadenoma", "syringoadenoma", "Hidradenoma, NOS", "eccrine acrospiroma", "sweat gland adenoma", "Sweat gland adenoma", "hidradenoma of skin", "Eccrine acrospiroma", "Eccrine Acrospiroma", "Hidradenoma of skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hidradenoma", "shortest_name_length": 11}
{"curie": "UMLS:C4526584", "names": ["Stage I Thymus Epithelial Neoplasm", "Stage I Thymic Epithelial Neoplasm AJCC v8", "Stage I Thymus Epithelial Neoplasm AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Thymic Epithelial Neoplasm AJCC v8", "shortest_name_length": 34}
{"curie": "MONDO:0021009", "names": ["Salivary Gland Mucoepidermoid Carcinoma", "salivary gland mucoepidermoid carcinoma", "Mucoepidermoid Carcinoma of Salivary Gland", "mucoepidermoid carcinoma of salivary gland", "Mucoepidermoid carcinoma of salivary gland", "mucoepidermoid carcinoma of the salivary gland", "Mucoepidermoid Carcinoma of the Salivary Gland", "saliva-secreting gland mucoepidermoid carcinoma", "Mucoepidermoid carcinoma of salivary gland (disorder)", "mucoepidermoid carcinoma of salivary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "salivary gland mucoepidermoid carcinoma", "shortest_name_length": 39}
{"curie": "UMLS:C4545065", "names": ["Large intestine infection", "infection of large intestine", "Infection of large intestine", "Infection of large intestine (disorder)", "infection of large intestine (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infection of large intestine", "shortest_name_length": 25}
{"curie": "MONDO:0003072", "names": ["Retina tumor", "Retina Tumor", "Retinal Tumor", "Retina tumour", "retinal tumor", "retina cancer", "Retinal tumor", "Retinal Cancer", "Retinal Tumors", "Retina--Cancer", "retinal cancer", "Tumor, Retinal", "Tumor of Retina", "Tumor of retina", "Cancer, Retinal", "Tumors, Retinal", "Retinal Cancers", "Retina Neoplasm", "Tumour of retina", "Retinal Neoplasm", "Cancers, Retinal", "Retinal neoplasm", "cancer of retina", "Neoplasm, Retinal", "Retinal Neoplasms", "Neoplasm of Retina", "neoplasm of retina", "Neoplasm of retina", "Neoplasms, Retinal", "eye neoplasm retina", "Tumor of the Retina", "Cancer of the Retina", "Neoplasm of the Retina", "malignant retina tumor", "Malignant Retina Tumor", "malignant retinal tumor", "Malignant Retinal Tumor", "Malignant retinal tumor", "Malignant retinal tumour", "Malignant Retina Neoplasm", "malignant retina neoplasm", "Malignant Tumor of Retina", "Malignant tumor of retina", "malignant tumor of retina", "Malignant tumour of retina", "malignant Retinal neoplasm", "malignant retinal neoplasm", "Malignant Retinal Neoplasm", "Malignant Neoplasm of Retina", "malignant neoplasm of retina", "Malignant neoplasm of retina", "Malignant Tumor of the Retina", "Neoplasm of retina (disorder)", "malignant tumor of the retina", "Neoplasm of retina (diagnosis)", "Malignant neoplasm of retina NOS", "malignant neoplasm of the retina", "Malignant Neoplasm of the Retina", "Malignant tumor of retina (disorder)", "malignant neoplasm of retina (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal cancer", "shortest_name_length": 12}
{"curie": "MONDO:0001885", "names": ["lateral cystocele", "Lateral cystocele", "Cystocele, lateral", "Lateral cystocele (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lateral cystocele", "shortest_name_length": 17}
{"curie": "UMLS:C5419174", "names": ["COVID-19-Associated Coagulopathy", "SARS-CoV-2-Associated Coagulopathy", "COVID-19-Associated Coagulation Disorder", "SARS-CoV-2-Associated Coagulation Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "COVID-19-Associated Coagulation Disorder", "shortest_name_length": 32}
{"curie": "MONDO:0019607", "names": ["unspecified JIA", "unspecified juvenile idiopathic arthritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "unspecified juvenile idiopathic arthritis", "shortest_name_length": 15}
{"curie": "MONDO:0013943", "names": ["PBD8B", "Peroxisome Biogenesis Disorder 8B", "PEROXISOME BIOGENESIS DISORDER 8B", "peroxisome biogenesis disorder 8B", "peroxisome biogenesis disorder type 8B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder 8B", "shortest_name_length": 5}
{"curie": "UMLS:C2930927", "names": ["Kallmann Syndrome 3", "Kallmann Syndrome, Type 3, Recessive", "Kallmann syndrome, type 3, recessive", "Autosomal Recessive Form of Kallmann Syndrome", "Hypogonadotropic Hypogonadism, Anosmia, and Midline Cranial Anomalies (Cleft Lip, Cleft Palate and Imperfect Fusion)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kallmann syndrome, type 3, recessive", "shortest_name_length": 19}
{"curie": "UMLS:C1699328", "names": ["Spermatic cord anastomotic leak", "anastomotic leak spermatic cord", "anastomotic leak of spermatic cord", "Spermatic Cord Anastomotic Leakage", "anastomotic leak of spermatic cord (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spermatic Cord Anastomotic Leakage", "shortest_name_length": 31}
{"curie": "MONDO:0009380", "names": ["DJS", "HBLRDJ", "Dubin-Johnson", "Dubin-Sprinz disease", "hyperbilirubinemia 2", "Hyperbilirubinemia 2", "DUBIN-SPRINZ DISEASE", "Hyperbilirubinemia 2s", "Spinz-Nelson syndrome", "Hyperbilirubinemia II", "Dubin-Sprinz syndrome", "HYPERBILIRUBINEMIA II", "DUBIN-JOHNSON SYNDROME", "Dubin-Johnson syndrome", "Sprinz Nelson syndrome", "dubin-johnson syndrome", "Hyperbilirubinaemia II", "Dubin-Johnson Syndrome", "Sprinz-Nelson syndrome", "DUBIN JOHNSON SYNDROME", "Dubin Johnson syndrome", "dubin johnson syndrome", "Hyperbilirubinemia IIs", "Dubin Johnson Syndrome", "dubin johnsons syndrome", "Syndrome, Dubin-Johnson", "hyperbilirubinemia type 2", "Hyperbilirubinemia type 2", "chronic idiopathic jaundice", "Chronic Idiopathic Jaundice", "CHRONIC IDIOPATHIC JAUNDICE", "Chronic idiopathic jaundice", "Jaundice, Chronic Idiopathic", "Idiopathic Jaundice, Chronic", "DJS - Dubin-Johnson syndrome", "Chronic Idiopathic Jaundices", "Jaundices, Chronic Idiopathic", "Idiopathic Jaundices, Chronic", "conjugated hyperbilirubinemia", "Black liver-jaundice syndrome", "Dubin-Johnson syndrome (disorder)", "Dubin-Johnson syndrome (diagnosis)", "Icterus-hepatic pigmentation syndrome", "HYPERBILIRUBINEMIA, DUBIN-JOHNSON TYPE", "hyperbilirubinemia, Dubin-Johnson type", "Chronic idiopathic jaundice with pigmented liver"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dubin-Johnson syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0001986", "names": ["Argyll Robertson pupil", "atypical; Argyll Robertson", "Argyll Robertson; atypical", "atypical Argyll-Robertson pupil", "Atypical Argyll-Robertson pupil", "Argyll Robertson pupil, atypical", "Nonsyphilitic Argyll-Robertson phenomenon", "Atypical Argyll-Robertson pupil (disorder)", "Argyll Robertson pupil, atypical (diagnosis)", "Argyll Robertson phenomenon or pupil, nonsyphilitic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Argyll Robertson pupil", "shortest_name_length": 22}
{"curie": "MONDO:0035943", "names": ["B-ALL with hyperdiploidy", "B lymphoblastic leukemia/lymphoma with hyperdiploidy", "B-Lymphoblastic Leukemia/Lymphoma with Hyperdiploidy", "B lymphoblastic leukemia lymphoma with hyperdiploidy", "B Lymphoblastic Leukemia/Lymphoma with Hyperdiploidy", "B-lymphoblastic leukemia/lymphoma with hyperdiploidy", "B lymphoblastic leukaemia lymphoma with hyperdiploidy", "B lymphoblastic leukemia lymphoma with hyperdiploidy (disorder)", "B lymphoblastic leukemia lymphoma with hyperdiploidy (diagnosis)", "B lymphoblastic leukemia lymphoma with hyperdiploidy (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-lymphoblastic leukemia/lymphoma with hyperdiploidy", "shortest_name_length": 24}
{"curie": "MONDO:0012146", "names": ["Hlh3", "HLH3", "FHL3", "Hplh3", "HPLH3", "familial hemophagocytic lymphohistiocytosis 3", "HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 3", "hemophagocytic lymphohistiocytosis, familial, 3", "Hemophagocytic lymphohistiocytosis, familial, 3", "UNC13D genetic hemophagocytic lymphohistiocytosis", "familial hemophagocytic lymphohistiocytosis type 3", "hemophagocytic lymphohistiocytosis, familial, type 3", "genetic hemophagocytic lymphohistiocytosis caused by mutation in UNC13D"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial hemophagocytic lymphohistiocytosis 3", "shortest_name_length": 4}
{"curie": "UMLS:C5447648", "names": ["Unresectable Lung Carcinoid Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Lung Carcinoid Tumor", "shortest_name_length": 33}
{"curie": "UMLS:C1399310", "names": ["Spinal cord hematoma", "hematoma; spinal cord", "spinal cord; hematoma", "Spinal cord haematoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spinal cord hematoma", "shortest_name_length": 20}
{"curie": "UMLS:C1520078", "names": ["Vulvar Deep Angiomyxoma", "Vulvar Aggressive Angiomyxoma", "Vulvar Deep \"Aggressive\" Angiomyxoma", "Vulvar Deep (Aggressive) Angiomyxoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Deep (Aggressive) Angiomyxoma", "shortest_name_length": 23}
{"curie": "UMLS:C0014574", "names": ["physitis", "Physitis", "EPIPHYSITIS", "epiphysitis", "Epiphysitis", "Epiphysitis NOS", "Epiphysitis, NOS", "Physeal dysplasia", "PHYSEAL DYSPLASIA", "Physeal Dysplasia", "Epiphysitis (disorder)", "Dysplasia of growth plate", "Epiphysitis not specified as adult or juvenile, of unspecified site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epiphysitis", "shortest_name_length": 8}
{"curie": "MONDO:0018408", "names": ["Hydatidoses", "Hydatidosis", "Hydatid Cyst", "Cyst, Hydatid", "Hydatid Cysts", "Cysts, Hydatid", "Hydatid disease", "Hydatid Disease", "hydatid disease", "Hydatid Diseases", "Cystic Echinocccosis", "Cystic Echinococcosis", "Cystic Echinococcoses", "Cystic echinococcosis", "cystic echinococcosis", "Echinococcosis, Cystic", "Echinococcoses, Cystic", "echinococcus granulosus", "unilocular echinococcosis", "Unilocular echinococcosis", "unilocular hydatid disease", "lung echinococcus granulosus", "Liver echinococcus granulosus", "liver echinococcus granulosus", "echinococcus granulosus of lung", "Thyroid echinococcus granulosus", "thyroid echinococcus granulosus", "Cystic echinococcosis (disorder)", "Echinococcus Granulosus Infection", "Echinococcus granulosus infection", "echinococcus granulosus of thyroid", "Echinococcus Granulosus Infections", "Infection, Echinococcus Granulosus", "Granulosus Infection, Echinococcus", "Granulosus Infections, Echinococcus", "Infections, Echinococcus Granulosus", "Echinococcus granulosus lung infection", "Echinococcus granulosus infection of lung", "echinococcus granulosus infectious disease", "Echinococcus granulosus pulmonary infection", "thyroid; Echinococcus granulosus (etiology)", "echinococcus granulosus of lung (diagnosis)", "Echinococcus granulosus infection of thyroid", "Echinococcus; granulosus, thyroid (etiology)", "echinococcus granulosus of thyroid (diagnosis)", "Echinococcus granulosus thyroid gland infection", "Echinococcus granulosus infection, thyroid gland", "thyroid; Echinococcus granulosus (manifestation)", "echinococcus granulosus infectious disease of liver", "Echinococcus granulosus infectious disease of liver", "Echinococcus granulosus infection of lung (disorder)", "echinococcus granulosus infectious disease of thyroid", "Echinococcus granulosus infection of thyroid (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cystic echinococcosis", "shortest_name_length": 11}
{"curie": "UMLS:C5447285", "names": ["Vulvar Angiosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Angiosarcoma", "shortest_name_length": 19}
{"curie": "MONDO:0003724", "names": ["non-proliferative fibrocystic change", "Non-Proliferative Fibrocystic Change", "Non-Proliferative Fibrocystic Change of Breast", "non-proliferative fibrocystic change of breast", "breast fibrocystic change, non-proliferative type", "Breast Fibrocystic Change, Non-Proliferative Type", "Non-Proliferative Fibrocystic Change of the Breast", "non-proliferative fibrocystic change of the breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-proliferative fibrocystic change of the breast", "shortest_name_length": 36}
{"curie": "UMLS:C2987142", "names": ["PanIN-1A", "Pancreatic Intraepithelial Neoplasia-1A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Intraepithelial Neoplasia-1A", "shortest_name_length": 8}
{"curie": "UMLS:C0393947", "names": ["cholinergic crisis", "Cholinergic crisis", "Cholinergic paralysis", "Cholinergic crisis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cholinergic crisis", "shortest_name_length": 18}
{"curie": "MONDO:0025100", "names": ["mastitis bovine", "Bovine Mastitis", "bovine mastitis", "Mastitis, Bovine", "mastitis, bovine", "bovine Mastitides", "Bovine Mastitides", "Mastitides, Bovine", "Mastitides, bovine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mastitis, bovine", "shortest_name_length": 15}
{"curie": "MONDO:0004541", "names": ["pseudoglandular variant testicular seminoma", "Testicular Seminoma, Pseudoglandular Variant", "testicular seminoma, pseudoglandular variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudoglandular variant testicular seminoma", "shortest_name_length": 43}
{"curie": "MONDO:0006849", "names": ["MASTITIS", "Mammitis", "mastitis", "Mastitis", "Mastitis NOS", "Mastitis, NOS", "breast infection", "INFECTION BREAST", "Infection breast", "BREAST INFECTION", "Breast infection", "infection breast", "breast; infection", "Breast infections", "breast infections", "infection; mammary", "Breast inflammation", "BREAST INFLAMMATION", "breast inflammation", "mastitis (diagnosis)", "Breast infection NOS", "inflammation of breast", "Inflammatory breast disease", "Breast infection (disorder)", "inflammatory breast disease", "Breast infection (diagnosis)", "inflammatory disease of breast", "Inflammatory disease of breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mastitis", "shortest_name_length": 8}
{"curie": "UMLS:C3671878", "names": ["Cystine Urolithiasis", "Cystine urolithiasis", "Cystine urolithiasis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cystine urolithiasis", "shortest_name_length": 20}
{"curie": "UMLS:C3273124", "names": ["Gallbladder Tubular Carcinoid", "Gallbladder Tubular Carcinoid Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gallbladder Tubular Carcinoid", "shortest_name_length": 29}
{"curie": "UMLS:C0432267", "names": ["syndrome tay", "tay syndrome", "Tay syndrome", "Tay Syndrome", "syndrome tays", "IBIDS Syndrome", "IBIDS Syndromes", "Tricho-thiodystrophy", "trichothiodystrophy 2", "trichothiodystrophy 2 (TTD 2)", "sulfur-deficient brittle hair syndrome", "Trichothiodystrophy with Congenital Ichtyosis", "congenital ichthyosis-trichodystrophy syndrome", "Recessive congenital ichthyosiform erythroderma", "trichothiodystrophy-congenital ichthyosis syndrome", "trichothiodystrophy-xeroderma pigmentosum syndrome", "Ichthyosiform erythroderma with hair abnormality, mental and growth retardation", "ichthyosiform erythroderma-hair abnormality-mental and growth retardation syndrome", "Ichthyosiform Erythroderma with Hair Abnormality and Mental and Growth Retardation", "Ichthyosis, Brittle Hair, Intellectual Impairment, Decreased Fertility, and Short Stature", "IBIDS (ichthyosis-brittle hair-impaired intelligence-decreased fertility-short stature) syndrome", "PIBI(D)S [photosensitivity-ichthyosis-brittle hair-impaired intelligence-(possibly decreased fertility)-short stature] syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IBIDS Syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0019293", "names": ["Vascular Skin Disease", "Skin vascular disease", "skin vascular disease", "vascular skin disease", "Vascular skin disorder", "skin vascular disorder", "Vascular Skin Diseases", "Skin Disease, Vascular", "Skin Vascular Disorder", "Skin Diseases, Vascular", "vasculature skin disease", "vascular disease of skin", "Vascular skin abnormality", "vascular disorder of skin", "Vascular disorder of skin", "Vascular disorders of skin", "Skin vascular malformation", "vascular disorders of skin", "Vascular skin condition NOS", "Skin vascular abnormalities", "Vascular disease of the skin", "vascular disease of the skin", "VASCULAR DISEASES OF THE SKIN", "Vascular disorder of skin, NOS", "superficial vasculature disease", "Vascular disease of the skin, NOS", "peripheral vascular disease of skin", "vascular disease of skin (diagnosis)", "Vascular disease of the skin (disorder)", "disorder of blood vessels affecting skin", "Disorder of blood vessels affecting skin", "Vascular abnormalities restricted to skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin vascular disease", "shortest_name_length": 21}
{"curie": "MONDO:0018054", "names": ["ATFB", "familial atrial fibrillation", "Familial Atrial Fibrillation", "Familial atrial fibrillation", "Fibrillation, Familial Atrial", "Atrial Fibrillation, Familial", "atrial fibrillation, familial", "Familial Atrial Fibrillations", "Atrial Fibrillations, Familial", "Fibrillations, Familial Atrial", "atrial fibrillation autosomal dominant", "autosomal dominant atrial fibrillation", "Familial atrial fibrillation (disorder)", "familial atrial fibrillation (diagnosis)", "hereditary atrial fibrillation (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial atrial fibrillation", "shortest_name_length": 4}
{"curie": "MONDO:0006809", "names": ["cerebral emboli", "Cerebral Emboli", "Embolus cerebral", "Emboli, Cerebral", "Cerebral Embolus", "cerebral embolus", "EMBOLUS CEREBRAL", "Cerebral embolus", "Embolism cerebral", "Cerebral Embolism", "Embolus, Cerebral", "CEREBRAL EMBOLISM", "cerebral embolism", "Cerebral embolism", "EMBOLISM CEREBRAL", "Embolism;cerebral", "cerebral; embolism", "embolism; cerebral", "EMBOLISM, CEREBRAL", "cerebral embolisms", "Embolism, Cerebral", "intracranial embolism", "Intracranial Embolism", "Embolism, Intracranial", "embolism; intracranial", "intracranial; embolism", "Cerebral artery embolism", "cerebral artery embolism", "embolism; cerebral artery", "arteries cerebral embolism", "Cerebral arterial embolism", "embolism of cerebral artery", "Cerebral embolism (disorder)", "cerebral embolism (diagnosis)", "intracranial embolism (diagnosis)", "Cerebral embolism (vessel unspecified)", "cerebral embolism with cerebral infarction", "Cerebral embolism with cerebral infarction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intracranial embolism", "shortest_name_length": 15}
{"curie": "MONDO:0012555", "names": ["CDLS3", "Cornelia de Lange syndrome 3", "Cornelia de Lange Syndrome 3", "CORNELIA DE LANGE SYNDROME 3", "Cornelia DE Lange syndrome 3", "Smc3 Cornelia de Lange syndrome", "SMC3 Cornelia de Lange syndrome", "Cornelia De Lange syndrome type 3", "Cornelia de Lange syndrome caused by mutation in Smc3", "Cornelia de Lange syndrome caused by mutation in SMC3", "Cornelia De Lange syndrome 3 with or without midline brain defects", "CORNELIA DE LANGE SYNDROME 3 WITH OR WITHOUT MIDLINE BRAIN DEFECTS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cornelia de Lange syndrome 3", "shortest_name_length": 5}
{"curie": "MONDO:0022636", "names": ["candida glabrata", "candida glabrata infection", "Torulopsis glabrata (formerly)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "candida glabrata infection", "shortest_name_length": 16}
{"curie": "MONDO:0005879", "names": ["ocular toxoplasmosis", "Ocular Toxoplasmoses", "Ocular Toxoplasmosis", "Ocular toxoplasmosis", "Toxoplasmoses, Ocular", "Toxoplasma oculopathy", "Toxoplasmosis, Ocular", "Eye infection toxoplasmal", "Ocular toxoplasmosis (disorder)", "Toxoplasma oculopathy, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ocular toxoplasmosis", "shortest_name_length": 20}
{"curie": "UMLS:C1336718", "names": ["testicular yolk sac tumor and embryonal carcinoma", "testicular embryonal carcinoma and yolk sac tumor", "embryonal carcinoma and yolk sac tumor, testicular", "yolk sac tumor and embryonal carcinoma of the testis", "testis cancer, embryonal carcinoma and yolk sac tumor", "testis cancer, yolk sac tumor and embryonal carcinoma", "Mixed Embryonal Carcinoma and Yolk Sac Tumor of Testis", "Testicular Mixed Embryonal Carcinoma and Yolk Sac Tumor", "testicle cancer, yolk sac tumor and embryonal carcinoma", "testicular cancer, embryonal carcinoma and yolk sac tumor", "Mixed Embryonal Carcinoma and Yolk Sac Neoplasm of Testis", "testicular cancer, yolk sac tumor and embryonal carcinoma", "Mixed Embryonal Carcinoma and Yolk Sac Tumor of the Testis", "Testicular Mixed Embryonal Carcinoma and Yolk Sac Neoplasm", "Mixed Embryonal Carcinoma and Yolk Sac Neoplasm of the Testis", "Mixed Embryonal Carcinoma and Endodermal Sinus Tumor of Testis", "Testicular Mixed Embryonal Carcinoma and Endodermal Sinus Tumor", "Mixed Embryonal Carcinoma and Endodermal Sinus Neoplasm of Testis", "Mixed Embryonal Carcinoma and Endodermal Sinus Tumor of the Testis", "Testicular Mixed Embryonal Carcinoma and Endodermal Sinus Neoplasm", "Mixed Embryonal Carcinoma and Endodermal Sinus Neoplasm of the Testis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular Mixed Embryonal Carcinoma and Yolk Sac Tumor", "shortest_name_length": 49}
{"curie": "UMLS:C0948016", "names": ["Soft tissue bleeding", "Soft tissue hemorrhage", "Soft tissue haemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Soft tissue hemorrhage", "shortest_name_length": 20}
{"curie": "UMLS:C5419139", "names": ["Immediately Life-Threatening Disorder", "immediately life-threatening disease or condition", "Immediately Life-Threatening Disease or Condition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immediately Life-Threatening Disorder", "shortest_name_length": 37}
{"curie": "MONDO:0002409", "names": ["auditory disease", "auditory system disease", "ear and mastoid disease", "auditory system disorder", "disease of auditory system", "disorder of auditory system", "auditory system disease or disorder", "disease or disorder of auditory system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "auditory system disorder", "shortest_name_length": 16}
{"curie": "UMLS:C0334610", "names": ["Hemangiopericytic meningioma", "Hemangiopericytic Meningioma", "meningioma; hemangiopericytic", "hemangiopericytic; meningioma", "Meningioma, Hemangiopericytic", "Haemangiopericytic meningioma", "Hemangiopericytic Meningiomas", "Meningiomas, Hemangiopericytic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemangiopericytic Meningioma", "shortest_name_length": 28}
{"curie": "MONDO:0037748", "names": ["hyperlipidemia", "Hyperlipoproteinemia", "hyperlipoproteinemia", "HYPERLIPOPROTEINEMIA", "Hyperlipoproteinaemia", "hyperlipoproteinaemia", "hyperlipoproteinemias", "Hyperlipoproteinemias", "hyperlipoproteinaemias", "Hyperlipoproteinemia NOS", "Hyperlipoproteinemia, NOS", "Hyperlipoproteinaemia, NOS", "hyperlipidemia (diagnosis)", "Hyperlipoproteinemia (disorder)", "hyperlipoproteinemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperlipoproteinemia", "shortest_name_length": 14}
{"curie": "MONDO:0031011", "names": ["NEDDFAS", "NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND VARIABLE SEIZURES", "neurodevelopmental disorder with dysmorphic facies and variable seizures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with dysmorphic facies and variable seizures", "shortest_name_length": 7}
{"curie": "MONDO:0007482", "names": ["dyschondrosteosis nephritis", "dyschondrosteosis and nephritis", "DYSCHONDROSTEOSIS AND NEPHRITIS", "Dyschondrosteosis and Nephritis", "dyschondrosteosis-nephritis syndrome", "mesomelic shortening and hereditary nephritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyschondrosteosis-nephritis syndrome", "shortest_name_length": 27}
{"curie": "UMLS:C5420274", "names": ["Oropharyngeal Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oropharyngeal Hodgkin Lymphoma", "shortest_name_length": 30}
{"curie": "UMLS:C5237920", "names": ["Benign Musculoskeletal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Musculoskeletal Neoplasm", "shortest_name_length": 31}
{"curie": "MONDO:0010351", "names": ["FA2", "FACB", "FANCB", "Fanconi pancytopenia type 2", "FANCONI PANCYTOPENIA, TYPE 2", "Fanconi Pancytopenia, Type 2", "Fanconi pancytopenia, type 2", "Fanconi anemia complementation group B", "Fanconi Anemia, Complementation Group B", "FANCONI ANEMIA, COMPLEMENTATION GROUP B", "Fanconi anemia, complementation group B", "Fanconi anemia complementation group type B", "Fanconi Anemia, complementation group type B", "Fanconi anemia complementation group B (diagnosis)", "Fanconi anemia, complementation group B, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fanconi anemia complementation group B", "shortest_name_length": 3}
{"curie": "MONDO:0020300", "names": ["ENFL", "Adnfle", "ADNFLE", "frontal lobe epilepsy autosomal dominant nocturnal", "Autosomal Dominant Nocturnal Frontal Lobe Epilepsy", "autosomal dominant nocturnal frontal lobe epilepsy", "Autosomal dominant nocturnal frontal lobe epilepsy", "Autosomal dominant sleep-related hypermotor epilepsy", "ADNFLE - Autosomal dominant nocturnal frontal lobe epilepsy", "Autosomal dominant nocturnal frontal lobe epilepsy (disorder)", "Autosomal dominant nocturnal frontal lobe epilepsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nocturnal frontal lobe epilepsy", "shortest_name_length": 4}
{"curie": "MONDO:0003627", "names": ["rheumatic pulmonary incompetence", "Rheumatic pulmonary incompetence", "Rheumatic pulmonary valve disease", "rheumatic pulmonary valve disease", "pulmonary valve disease rheumatic", "Rheumatic disease of pulmonary valve", "rheumatic disease of pulmonary valve", "Rheumatic diseases of pulmonary valve", "pulmonary valve rheumatologic disorder", "Rheumatic pulmonary valve disease, NOS", "rheumatologic disorder of pulmonary valve", "Rheumatic disease of pulmonary valve, NOS", "Rheumatic disease of pulmonary valve (disorder)", "rheumatic disease of pulmonary valve (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rheumatic pulmonary valve disease", "shortest_name_length": 32}
{"curie": "MONDO:0003789", "names": ["HPRCC", "RCCP1", "renal cell carcinoma, papillary", "RENAL CELL CARCINOMA, PAPILLARY, 1", "Familial Renal Papillary Carcinoma", "familial renal papillary carcinoma", "Type 1 Papillary Renal Cell Cancer", "Hereditary Papillary Renal Carcinoma", "Hereditary papillary renal carcinoma", "Hereditary Papillary renal carcinoma", "hereditary papillary renal carcinoma", "Type 1 Papillary Renal Cell Carcinoma", "Papillary renal cell carcinoma type 1", "Hereditary Kidney Papillary Carcinoma", "hereditary kidney papillary carcinoma", "type 1 papillary renal cell carcinoma", "Hereditary Papillary Renal Cell Cancer", "hereditary papillary renal cell cancer", "Hereditary Papillary Carcinoma of Kidney", "hereditary papillary carcinoma of kidney", "Hereditary papillary renal cell carcinoma", "Hereditary Papillary Renal Cell Carcinoma", "hereditary papillary renal cell carcinoma", "Hereditary Papillary Carcinoma of the Kidney", "hereditary papillary carcinoma of the kidney", "Hereditary papillary renal cell carcinoma (disorder)", "renal cell carcinoma, papillary, 1, familial and somatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary papillary renal cell carcinoma", "shortest_name_length": 5}
{"curie": "UMLS:C5446669", "names": ["Locally Advanced Adenoid Cystic Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Adenoid Cystic Carcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0013144", "names": ["AT3D", "THPH7", "AT III deficiency", "AT-III deficiency", "antithrombin deficiency", "Antithrombin deficiency", "Antithrombin 3 deficiency", "antithrombin 3 deficiency", "antithrombin deficiencies", "Antithrombin 3 Deficiency", "Deficiency, Antithrombin 3", "Decreased antithrombin III", "Antithombin III deficiency", "Antithrombin III deficiency", "Antithrombin 3 Deficiencies", "antithrombin iii deficiency", "ANTITHROMBIN III DEFICIENCY", "Antithrombin III Deficiency", "antithrombin III deficiency", "Deficiency, Antithrombin III", "AT (antithrombin) deficiency", "congenital AT-III deficiency", "Anti-thrombin III deficiency", "Deficiencies, Antithrombin 3", "Antithrombin III Deficiencies", "Deficiencies, Antithrombin III", "Reduced antithrombin III activity", "inherited antithrombin deficiency", "hereditary antithrombin deficiency", "congenital antithrombin III deficiency", "Antithrombin III deficiency (disorder)", "AT deficiency - Antithrombin deficiency", "antithrombin III deficiency (diagnosis)", "thrombophilia due to antithrombin 3 deficiency", "THROMBOPHILIA DUE TO ANTITHROMBIN III DEFICIENCY", "thrombophilia due to antithrombin III deficiency", "thrombophilia 7 due to antithrombin III deficiency", "hereditary thrombophilia due to congenital antithrombin deficiency", "hereditary thrombophilia due to congenital antithrombin 3 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary antithrombin deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0005435", "names": ["anti-neutrophil antibody associated vasculitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anti-neutrophil antibody associated vasculitis", "shortest_name_length": 46}
{"curie": "MONDO:0016907", "names": ["Monosomy 8q", "8q monosomy", "deletion 8q", "Deletion 8q", "monosomy 8q", "8q deletion", "8q- syndrome", "del(8q) syndrome", "partial monosomy 8q", "8q deletion syndrome", "deletion 8q syndrome", "chromosome 8q monosomy", "chromosome 8q deletion", "Chromosome 8, monosomy 8q", "chromosome 8q deletion syndrome", "Partial deletion of chromosome 8q", "partial monosomy of chromosome 8q", "partial deletion of chromosome 8q", "Partial monosomy of chromosome 8q", "partial deletion of the long arm of chromosome 8", "Partial deletion of the long arm of chromosome 8", "Partial monosomy of the long arm of chromosome 8", "partial monosomy of the long arm of chromosome 8", "partial deletion of the long arm of chromosome type 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of the long arm of chromosome 8", "shortest_name_length": 11}
{"curie": "UMLS:C1332920", "names": ["Cervical Non-Neoplastic Disease", "Cervical Non-Neoplastic Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Non-Neoplastic Disorder", "shortest_name_length": 31}
{"curie": "MONDO:0026720", "names": ["MC1DN12", "nuclear type mitochondrial complex I deficiency 12", "mitochondrial complex 1 deficiency, nuclear type 12", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 12", "mitochondrial complex i deficiency, nuclear type 12, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 12", "shortest_name_length": 7}
{"curie": "MONDO:0012900", "names": ["RCM3", "Rcm3", "restrictive cardiomyopathy 3", "familial restrictive cardiomyopathy 3", "CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3", "cardiomyopathy, familial restrictive, 3", "Cardiomyopathy, Familial Restrictive, 3", "CARDIOMYOPATHY, FAMILIAL, RESTRICTIVE, 3", "cardiomyopathy, familial restrictive, type 3", "TNNT2 familial isolated restrictive cardiomyopathy", "CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)", "familial isolated restrictive cardiomyopathy caused by mutation in TNNT2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiomyopathy, familial restrictive, 3", "shortest_name_length": 4}
{"curie": "MONDO:0022892", "names": ["craniosynostosis alopecia brain defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniosynostosis alopecia brain defect", "shortest_name_length": 38}
{"curie": "UMLS:C4055502", "names": ["Acquired Hypogonadotropic Hypogonadism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired Hypogonadotropic Hypogonadism", "shortest_name_length": 38}
{"curie": "UMLS:C1334013", "names": ["High Grade Corneal Intraepithelial Neoplasia", "High Grade Corneal Squamous Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Corneal Squamous Intraepithelial Neoplasia", "shortest_name_length": 44}
{"curie": "UMLS:C0852336", "names": ["immunohemolytic anemia", "Immune hemolytic anemia", "immune hemolytic anemia", "anemia hemolytic immune", "Immune Hemolytic Anemia", "anemias hemolytic immune", "immune hemolytic anemias", "Anemias hemolytic immune", "Immune haemolytic anaemia", "Anaemias haemolytic immune", "immune complex hemolytic anemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immune Hemolytic Anemia", "shortest_name_length": 22}
{"curie": "MONDO:0017783", "names": ["Congenital pancreatic cyst", "PANCREAS, CYST, CONGENITAL", "congenital pancreatic cyst", "pancreatic cyst congenital", "cyst; pancreas, congenital", "Congenital cyst of pancreas", "True congenital pancreatic cyst", "true congenital pancreatic cyst", "Neonatal congenital pancreatic cyst", "neonatal congenital pancreatic cyst", "Congenital cyst of pancreas (disorder)", "congenital pancreatic cyst (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital pancreatic cyst", "shortest_name_length": 26}
{"curie": "UMLS:C0079757", "names": ["Diffuse Mixed Cell Lymphoma", "Diffuse Mixed-Cell Lymphoma", "Mixed-Cell Lymphoma, Diffuse", "Diffuse Mixed-Cell Lymphomas", "Mixed Cell Lymphoma, Diffuse", "Lymphoma, Diffuse Mixed-Cell", "Lymphoma, Mixed-Cell, Diffuse", "Lymphoma, Mixed Cell, Diffuse", "lymphoma; mixed cell type, diffuse", "lymphoma; diffuse, mixed cell type", "diffuse; lymphoma, mixed cell type", "Diffuse Mixed Small and Large Cell Lymphoma", "Diffuse Mixed Large and Small Cell Lymphoma", "Mixed Small and Large Cell Lymphoma, Diffuse", "Lymphoma, Mixed Small and Large Cell, Diffuse", "Diffuse mixed lymphocytic-histiocytic lymphoma", "Lymphoma, Small and Large Cleaved-Cell, Diffuse", "Lymphoma, Diffuse, Mixed Lymphocytic-Histiocytic", "small cell; lymphoma, with large cell, mixed (diffuse)", "lymphoma; small cell, with large cell, mixed (diffuse)", "lymphoma; diffuse, mixed cell type, small and large cell", "diffuse; lymphoma, mixed cell type, small and large cell", "lymphoma; mixed cell type, small and large cell (diffuse)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse Mixed-Cell Lymphoma", "shortest_name_length": 27}
{"curie": "UMLS:C4744708", "names": ["Parotid Gland Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parotid Gland Sarcoma", "shortest_name_length": 21}
{"curie": "UMLS:C2984067", "names": ["Renal Cell Cancer by AJCC v7 Stage", "Renal Cell Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal Cell Cancer by AJCC v7 Stage", "shortest_name_length": 34}
{"curie": "MONDO:0001466", "names": ["punctate keratitis", "Keratitis punctate", "Punctate keratitis", "PK - Punctate keratitis", "Punctate keratitis (disorder)", "Punctate epithelial keratitis", "Superficial punctate keratitis", "superficial punctate keratitis", "punctate keratitis (diagnosis)", "Thygeson superficial punctate keratitis", "punctate epithelial keratoconjunctivitis", "Punctate epithelial keratoconjunctivitis", "Thygeson's superficial punctate keratitis", "Thygeson superficial punctate keratopathy", "Thygeson superficial punctate keratitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "punctate epithelial keratoconjunctivitis", "shortest_name_length": 18}
{"curie": "MONDO:0001468", "names": ["Plica syndrome", "plica syndrome", "Plica Syndrome", "plica syndromes", "synovial plica of knee", "Synovial plica of knee", "Synovial Plica Syndrome", "synovial plica syndrome", "Plica Syndrome, Synovial", "plica syndrome (diagnosis)", "Synovial plica of knee (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "synovial plica syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C4688342", "names": ["Recurrent Grade III Glioma", "Recurrent WHO Grade 3 Glioma", "Recurrent WHO Grade III Glioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent WHO Grade 3 Glioma", "shortest_name_length": 26}
{"curie": "MONDO:0031008", "names": ["NPHS24", "idiopathic SRNS", "nephrotic syndrome, type 24", "NEPHROTIC SYNDROME, TYPE 24", "idiopathic steroid-resistant nephrotic syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrotic syndrome, type 24", "shortest_name_length": 6}
{"curie": "MONDO:0004984", "names": ["Basal-Like Breast Cancer", "basal-like breast cancer", "Basal-Like Breast Carcinoma", "basal-like breast carcinoma", "basal-like subtype of breast carcinoma", "Basal-Like Subtype of Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "basal-like breast carcinoma", "shortest_name_length": 24}
{"curie": "UMLS:C1336391", "names": ["Stage IVC Lip Basal Cell Cancer", "Stage IVC Basal Cell Lip Carcinoma", "Stage IVC Basal Cell Carcinoma of Lip", "stage IVC basal cell carcinoma of the lip", "Stage IVC Basal Cell Carcinoma of the Lip"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Basal Cell Lip Carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0014511", "names": ["CMT2S", "Charcot-Marie-Tooth disease type 2S", "IGHMBP2 Charcot-Marie-Tooth disease", "Charcot-Marie-Tooth neuropathy type 2S", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2S", "Charcot-Marie-Tooth neuropathy, type 2S", "Charcot-Marie-Tooth disease axonal type 2S", "Charcot-Marie-Tooth disease, axonal, type 2S", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2S", "Charcot-Marie-Tooth disease type 2S (disorder)", "autosomal recessive axonal Charcot-Marie-Tooth type 2S", "Charcot-Marie-Tooth disease caused by mutation in IGHMBP2", "Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2S", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2S"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease axonal type 2S", "shortest_name_length": 5}
{"curie": "UMLS:C0856088", "names": ["Constipation aggravated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Constipation aggravated", "shortest_name_length": 23}
{"curie": "UMLS:C4521728", "names": ["Stage IVA Esophageal Squamous Cell Cancer", "Clinical Stage IVA Esophageal Squamous Cell Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage IVA Esophageal Squamous Cell Carcinoma AJCC v8", "shortest_name_length": 41}
{"curie": "MONDO:0004601", "names": ["ankle ulcer", "Ankle ulcer", "ANKLE ULCER", "ankle ulcers", "Ulcer of calf", "ulcer on ankle", "Ulcer of ankle", "Ulcer of thigh", "ulcer of ankle", "ulcer of lower limbs", "Ankle ulcer (disorder)", "Ulcer of heel and midfoot", "ulcer of ankle (diagnosis)", "ulcer of ankle (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ulcer of lower limbs", "shortest_name_length": 11}
{"curie": "UMLS:C0234304", "names": ["Secondary sweet taste disorder", "Taste Disorder, Secondary, Sweet", "Taste disorder, secondary, sweet", "Secondary sweet taste disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Taste Disorder, Secondary, Sweet", "shortest_name_length": 30}
{"curie": "MONDO:0019386", "names": ["rubella panencephalitis", "Progressive rubella panencephalitis", "progressive rubella panencephalitis", "Progressive rubella panencephalitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive rubella panencephalitis", "shortest_name_length": 23}
{"curie": "UMLS:C4721425", "names": ["Recurrent Corpus Uteri Cancer", "Recurrent Uterine Corpus Cancer", "Recurrent Uterine (Including Endometrial) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Uterine Corpus Cancer", "shortest_name_length": 29}
{"curie": "MONDO:0600024", "names": ["IIM", "Idiopathic myopathy", "familial idiopathic myositis", "familial idiopathic inflammatory myopathy", "Myopathy, familial idiopathic inflammatory", "Idiopathic inflammatory myopathy, familial", "MYOPATHY, FAMILIAL IDIOPATHIC INFLAMMATORY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial idiopathic inflammatory myopathy", "shortest_name_length": 3}
{"curie": "MONDO:0019137", "names": ["non-24", "hypernychthemeral syndrome", "Non-24 hour sleep-wake cycle", "non-24-hour sleep-wake rhythm", "non 24 hour sleep wake disorder", "non-24-hour sleep-wake syndrome", "Free-running sleep-wake cycle disorder", "Non-24 hour sleep-wake cycle (disorder)", "non-24-hour sleep-wake rhythm (diagnosis)", "Circadian rhythm sleep disorder, free running", "circadian rhythm sleep disorder, free-running type", "circadian rhythm sleep disorder, free running type", "Circadian rhythm sleep disorder, free-running type", "Circadian rhythm sleep disorder, free running type", "sleep disorder circadian rhythm, free running type", "Circadian rhythm sleep disorder, free running type (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-24-hour sleep-wake syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0010456", "names": ["RCCX1", "renal cell carcinoma, papillary, 1", "renal cell carcinoma, Xp11-associated", "RENAL CELL CARCINOMA, Xp11-ASSOCIATED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal cell carcinoma, Xp11-associated", "shortest_name_length": 5}
{"curie": "MONDO:0018312", "names": ["Darling", "HISTOPLASMOSIS", "histoplasmosis", "Histoplasmosis", "histoplasmoses", "darling disease", "Darling disease", "Histoplasmosis NOS", "Histoplasmosis, NOS", "Histoplasma Infection", "Histoplasma; infection", "Histoplasma Infections", "infection; Histoplasma", "Histoplasma infections", "Infection, Histoplasma", "Darling; histoplasmosis", "histoplasmosis; Darling", "Infection histoplasmosis", "Histoplasmosis (disorder)", "histoplasmosis (diagnosis)", "Histoplasmosis, unspecified", "Histoplasma infectious disease", "Histoplasma disease or disorder", "Histoplasma caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "histoplasmosis", "shortest_name_length": 7}
{"curie": "UMLS:C0919882", "names": ["Incision site bleeding", "Incision site hemorrhage", "Incision site haemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Incision site hemorrhage", "shortest_name_length": 22}
{"curie": "UMLS:C1336184", "names": ["Stage IIB Large Cell Lung Cancer", "Stage IIB Large Cell Lung Carcinoma", "Stage IIB Large Cell Carcinoma of Lung", "Stage IIB Large Cell Carcinoma of the Lung", "Stage IIB Lung Large Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Lung Large Cell Carcinoma AJCC v7", "shortest_name_length": 32}
{"curie": "MONDO:0013753", "names": ["CMT2P", "Cmt2g", "CMT2G", "CMT 2G", "CMT2G, FORMERLY", "LRSAM1 Charcot-Marie-Tooth disease", "Charcot Marie Tooth disease type 2G", "Charcot-Marie-Tooth disease type 2P", "Charcot-Marie-Tooth disease type 2G", "Charcot-Marie-Tooth disease, Type 2G", "Charcot-Marie-Tooth neuropathy type 2P", "Charcot-Marie-Tooth Neuropathy, Type 2g", "Charcot-Marie-Tooth neuropathy, type 2G", "Charcot-Marie-Tooth neuropathy, type 2P", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2P", "Charcot-Marie-Tooth disease axonal type 2P", "CMT2P - Charcot-Marie-Tooth disease type 2P", "Charcot-Marie-Tooth disease, axonal, type 2G", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2P", "Charcot-Marie-Tooth disease, axonal, type 2P", "Charcot-Marie-Tooth disease, axonal, Type 2G", "Charcot-Marie-Toothe disease, axonal, type 2P", "Charcot-Marie-Tooth disease type 2P (disorder)", "Charcot-Marie-Tooth disease type 2P (diagnosis)", "Charcot-Marie-Tooth disease type 2G (diagnosis)", "Charcot-Marie-Tooth disease, type 4A, axonal form", "autosomal dominant Charcot-Marie-Tooth disease type 2G", "Autosomal dominant Charcot-Marie-Tooth disease type 2G", "Charcot-Marie-Tooth disease, axonal, type 2G, formerly", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2G, FORMERLY", "Charcot-Marie-Tooth disease caused by mutation in LRSAM1", "Autosomal dominant Charcot-Marie-Tooth disease type 2G (disorder)", "Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease axonal type 2P", "shortest_name_length": 5}
{"curie": "MONDO:0054723", "names": ["SPGF19", "SPERMATOGENIC FAILURE 19", "spermatogenic failure 19"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 19", "shortest_name_length": 6}
{"curie": "MONDO:0013148", "names": ["BRGDA8", "BRUGADA SYNDROME 8", "Brugada syndrome 8", "Brugada Syndrome 8", "HCN4 Brugada syndrome", "Brugada syndrome type 8", "Brugada syndrome 8 (diagnosis)", "Brugada syndrome caused by mutation in HCN4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brugada syndrome 8", "shortest_name_length": 6}
{"curie": "UMLS:C0156406", "names": ["post coital bleed", "bleeding postcoital", "Postcoital bleeding", "Bleeding;postcoital", "postcoital bleeding", "Postcoital Bleeding", "bleeding coital post", "bleeding post coital", "post coital bleeding", "Post coital bleeding", "postcoital; hemorrhage", "hemorrhage; postcoital", "bleed after intercourse", "PCB - Postcoital bleeding", "Bleeding after intercourse", "bleeding after intercourse", "after bleeding intercourse", "Postcoital bleeding (finding)", "postcoital bleeding (diagnosis)", "bleeding after sexual intercourse", "bleeding after sexual intercourse (symptom)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postcoital bleeding", "shortest_name_length": 17}
{"curie": "MONDO:0000451", "names": ["PPMS", "Primary-progressive MS", "primary-progressive MS", "Primary progressive multiple sclerosis", "Primary Progressive Multiple Sclerosis", "multiple sclerosis progressive primary", "primary progressive multiple sclerosis", "Multiple Sclerosis, Primary Progressive", "Multiple sclerosis (MS) primary progressive", "Primary progressive multiple sclerosis (disorder)", "Primary progressive multiple sclerosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary progressive multiple sclerosis", "shortest_name_length": 4}
{"curie": "MONDO:0019173", "names": ["LYSSA", "lyssa", "Lyssa", "RABIES", "Rabies", "Lyssas", "rabies", "hydrophobia", "Rabies, NOS", "HYDROPHOBIA", "Hydrophobia", "Lyssa - rabies", "Rabies (disorder)", "rabies (diagnosis)", "Rabies encephalitis", "Rabies, unspecified", "St Hubert's disease", "Rabies virus infection", "Rabies viral infections", "Infection due to Rabies virus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rabies", "shortest_name_length": 5}
{"curie": "UMLS:C2826543", "names": ["Halo Eczema", "Meyerson Nevus", "Halo Dermatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meyerson Nevus", "shortest_name_length": 11}
{"curie": "MONDO:0008753", "names": ["aku", "AKU", "Alcaptonuria", "Alkaptonuria", "ALKAPTONURIA", "alcaptonuria", "ALCAPTONURIA", "alkaptonuria", "Alcaptonurias", "Homogentisicaciduria", "HOMOGENTISICACIDURIA", "Homogentisic Acidura", "homogentisic acidura", "Hereditary ochronosis", "hereditary ochronosis", "Ochronosis, hereditary", "ochronosis, hereditary", "alkaptonuric ochronosis", "alkaptonuria (diagnosis)", "deficiency of homogentisicase", "Deficiency of homogentisicase", "Homogentisic Acid Oxidase Deficiency", "HOMOGENTISIC ACID OXIDASE DEFICIENCY", "Homogentisic acid oxidase deficiency", "homogentisic acid oxidase deficiency", "Deficiency of homogentisate oxygenase", "Homogentisate 1,2-dioxygenase deficiency", "homogentisate 1,2-dioxygenase deficiency", "homogentisate l,2-dioxygenase deficiency", "homogentisate 1,2-dioxygenase; deficiency", "deficiency; homogentisate 1,2-dioxygenase", "Deficiency of homogentisate 1,2-dioxygenase", "Homogentisate 1,2-dioxygenase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alkaptonuria", "shortest_name_length": 3}
{"curie": "UMLS:C1335661", "names": ["Radiation-Induced Angiosarcoma", "Radiation-Related Angiosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radiation-Related Angiosarcoma", "shortest_name_length": 30}
{"curie": "MONDO:0010039", "names": ["Sonoda syndrome", "SONODA SYNDROME", "Congenital heart defect-round face-developmental delay syndrome", "congenital heart defect-round face-developmental delay syndrome", "Congenital heart defect with round face and developmental delay syndrome", "Congenital heart defect with round face and developmental delay syndrome (disorder)", "round face with depressed nasal Bridge and small mouth, congenital heart defect, and retarded development", "ROUND FACE WITH DEPRESSED NASAL BRIDGE AND SMALL MOUTH, CONGENITAL HEART DEFECT, AND RETARDED DEVELOPMENT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital heart defect-round face-developmental delay syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0009414", "names": ["GSD0A", "GSD 0a", "GSD 0A", "GSD type 0", "GSD type 0a", "liver GSD 0", "glycogenosis type 0a", "glycogen synthase deficiency", "Glycogen synthase deficiency", "glycogen synthetase deficiency", "glycogen synthetase; deficiency", "glycogen storage disease type 0", "Glycogen storage disease type 0", "deficiency; glycogen synthetase", "Liver Glycogen Storage Disease 0", "liver glycogen storage disease 0", "glycogen storage disease type 0a", "LIVER GLYCOGEN STORAGE DISEASE 0", "GLYCOGEN STORAGE DISEASE 0, LIVER", "glycogen storage disease 0, liver", "Glycogen Storage Disease 0, Liver", "LIVER GLYCOGEN SYNTHASE DEFICIENCY", "Liver Glycogen Synthase Deficiency", "liver glycogen synthase deficiency", "Glycogen synthase deficiency disease", "hepatic glycogen synthase deficiency", "glycogen storage disease type 0, liver", "Glycogen synthase deficiency (disorder)", "glycogen synthetase deficiency (diagnosis)", "GSD due to hepatic glycogen synthase deficiency", "Hypoglycemia With Deficiency Of Glycogen Synthetase In The Liver", "hypoglycemia with deficiency of glycogen synthetase in the liver", "HYPOGLYCEMIA WITH DEFICIENCY OF GLYCOGEN SYNTHETASE IN THE LIVER", "glycogen storage disease due to liver glycogen synthase deficiency", "liver glycogen storage disease due to glycogen synthase deficiency", "glycogen storage disease due to hepatic glycogen synthase deficiency", "glycogen storage disease due to glycogen synthase deficiency of liver", "glycogen storage disorder due to hepatic glycogen synthase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disorder due to hepatic glycogen synthase deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C0948279", "names": ["Beta hemolytic streptococcal infection", "Beta haemolytic streptococcal infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Beta hemolytic streptococcal infection", "shortest_name_length": 38}
{"curie": "MONDO:0060650", "names": ["LCAEOD", "LEBER CONGENITAL AMAUROSIS AND EARLY-ONSET DEAFNESS", "LEBER CONGENITAL AMAUROSIS WITH EARLY-ONSET DEAFNESS", "Leber congenital amaurosis with early-onset deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leber congenital amaurosis with early-onset deafness", "shortest_name_length": 6}
{"curie": "UMLS:C0339383", "names": ["chorioretinopathy", "Chorioretinopathy", "Retinochoroidopathy", "Chorioretinal disorder", "Chorioretinal disorders", "Chorioretinal disorder NOS", "Chorioretinal disorder (disorder)", "Choroidal and chorioretinal disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chorioretinal disorder", "shortest_name_length": 17}
{"curie": "UMLS:C4744999", "names": ["Transformed Marginal Zone Lymphoma to Diffuse Large B-Cell Lymphoma", "Diffuse Large B-Cell Lymphoma Transformed from Underlying Marginal Zone Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transformed Marginal Zone Lymphoma to Diffuse Large B-Cell Lymphoma", "shortest_name_length": 67}
{"curie": "MONDO:0030088", "names": ["DEND2", "PNDM3", "diabetes mellitus, permanent neonatal 3", "DIABETES MELLITUS, PERMANENT NEONATAL 3", "DIABETES MELLITUS, PERMANENT NEONATAL, 3", "Developmental Delay, Epilepsy, and Neonatal Diabetes 2", "DEVELOPMENTAL DELAY, EPILEPSY, AND NEONATAL DIABETES 2", "diabetes mellitus, permanent neonatal 3, with or without neurologic features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diabetes mellitus, permanent neonatal 3", "shortest_name_length": 5}
{"curie": "UMLS:C0009041", "names": ["Simple dislocation of hip", "Closed Dislocation of Hip", "closed dislocation of hip", "Closed dislocation of hip", "Dislocation of hip, simple", "Closed dislocation of hip, NOS", "closed dislocation of hip (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Closed dislocation of hip", "shortest_name_length": 25}
{"curie": "UMLS:C0860621", "names": ["medical condition; causing delirium", "condition; medical as cause of delirium", "Delirium due to a general medical condition", "Delirium Due to a General Medical Condition", "delirium; general medical condition as cause", "delirium; caused by general medical condition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Delirium due to a general medical condition", "shortest_name_length": 35}
{"curie": "MONDO:0005392", "names": ["scoliosis", "Scoliosis", "SCOLIOSIS", "scolioses", "Scolioses", "Scoliosis,", "Scoliosis, NOS", "SPINE CURVATURE", "curvature spine", "spine curvature", "curvature; spine", "curvature spinal", "spinal curvature", "Spinal Curvature", "spine; curvature", "Spinal Curvatures", "spinal curvatures", "Curvature, Spinal", "Curvature of spine", "Curvatures, Spinal", "CURVATURE OF SPINE", "curvature of spine", "Acquired scoliosis", "Unspecified scoliosis", "scoliosis (diagnosis)", "Scoliosis, unspecified", "Curvature of spine NOS", "Curvature of spine, NOS", "Scoliosis deformity of spine", "Scoliosis deviation of spine", "Acquired scoliosis (disorder)", "Curvature of spine (disorder)", "Unspecified curvature of spine", "curvature of spine (diagnosis)", "Idiopathic curvature of spine NOS", "Scoliosis deformity of spine (disorder)", "lateral curvature of the spine developed after birth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scoliosis", "shortest_name_length": 9}
{"curie": "MONDO:0010459", "names": ["ALS15", "ALS15 (diagnosis)", "amyotrophic lateral sclerosis 15", "amyotrophic lateral sclerosis ALS15", "UBQLN2 amyotrophic lateral sclerosis", "amyotrophic lateral sclerosis type 15", "amyotrophic lateral sclerosis caused by mutation in UBQLN2", "amyotrophic lateral sclerosis 15 with or without frontotemporal dementia", "AMYOTROPHIC LATERAL SCLEROSIS 15 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA", "AMYOTROPHIC LATERAL SCLEROSIS 15, WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA", "amyotrophic lateral sclerosis 15, with or without frontotemporal dementia", "amyotrophic lateral sclerosis 15, with or without frontotemporal dementia, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyotrophic lateral sclerosis type 15", "shortest_name_length": 5}
{"curie": "UMLS:C2363784", "names": ["Recurrence of neuromuscular blockade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrence of neuromuscular blockade", "shortest_name_length": 36}
{"curie": "MONDO:0021444", "names": ["benign colorectal tumor", "Benign Colorectal Tumor", "benign large bowel tumor", "Benign Colorectal Tumors", "Benign Large Bowel Tumor", "benign colorectal tumors", "colorectal tumors, benign", "Colorectal Tumors, Benign", "Tumors, Colorectal, Benign", "benign colorectal neoplasm", "tumors, colorectal, benign", "Benign Colorectal Neoplasm", "benign tumor of large bowel", "Benign Colorectal Neoplasms", "Benign Large Bowel Neoplasm", "benign large bowel neoplasm", "benign colorectal neoplasms", "Benign Tumor of Large Bowel", "Colorectal Neoplasms, Benign", "Benign Large Intestine Tumor", "colorectal neoplasms, benign", "benign large intestine tumor", "neoplasms, colorectal, benign", "Neoplasms, Colorectal, Benign", "benign neoplasm of large bowel", "Benign Neoplasm of Large Bowel", "benign tumor of the large bowel", "Benign Tumor of the Large Bowel", "Benign Large Intestine Neoplasm", "Benign Tumor of Large Intestine", "benign large intestine neoplasm", "benign tumor of large intestine", "Large intestine benign neoplasm", "large intestine benign neoplasm", "Benign tumor of large intestine", "Benign tumour of large intestine", "Benign neoplasm of large intestine", "benign neoplasm of large intestine", "Benign Neoplasm of Large Intestine", "Benign Neoplasm of the Large Bowel", "benign neoplasm of the large bowel", "Benign Tumor of the Large Intestine", "benign tumor of the large intestine", "Benign Neoplasm of the Large Intestine", "Benign neoplasm of large intestine NOS", "benign neoplasm of the large intestine", "Benign neoplasm of large intestine, NOS", "Benign neoplasm of large intestine (disorder)", "benign neoplasm of large intestine (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of large intestine", "shortest_name_length": 23}
{"curie": "UMLS:C0155842", "names": ["Peripharyngeal abscess", "Parapharyngeal abscess", "PARAPHARYNGEAL ABSCESS", "Parapharyngeal Abscess", "abscess; peripharyngeal", "peripharyngeal; abscess", "parapharyngeal; abscess", "Parapharyngeal abscess NOS", "Lateral Pharyngeal Abscess", "abscess of parapharyngeal space", "Abscess of parapharyngeal space", "Parapharyngeal abscess (disorder)", "Abscess of lateral pharyngeal space", "abscess of parapharyngeal space (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parapharyngeal abscess", "shortest_name_length": 22}
{"curie": "MONDO:0035337", "names": ["DRS with deafness", "DURS with deafness", "DRS with hearing loss", "DURS with hearing loss", "Duane retraction syndrome with congenital deafness", "Duane retraction syndrome with congenital hearing loss"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Duane retraction syndrome with congenital deafness", "shortest_name_length": 17}
{"curie": "UMLS:C5418755", "names": ["Recurrent Malignant Breast Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Malignant Breast Neoplasm", "shortest_name_length": 35}
{"curie": "MONDO:0024645", "names": ["Retroperitoneal Neoplasm", "retroperitoneal neoplasm", "retroperitoneal space tumor", "tumor of retroperitoneal space", "retroperitoneal space neoplasm", "neoplasm of retroperitoneal space"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retroperitoneal neoplasm", "shortest_name_length": 24}
{"curie": "UMLS:C1696704", "names": ["Ovarian bleeding", "Ovarian Hemorrhage", "Ovarian hemorrhage", "ovarian hemorrhage", "Ovarian haemorrhage", "ovarian hemorrhage (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Hemorrhage", "shortest_name_length": 16}
{"curie": "MONDO:0011286", "names": ["DFNB13", "autosomal recessive deafness 13", "Deafness, Autosomal Recessive 13", "DEAFNESS, AUTOSOMAL RECESSIVE 13", "deafness, autosomal recessive 13", "autosomal recessive nonsyndromic deafness 13", "autosomal recessive nonsyndromic hearing loss 13", "autosomal recessive nonsyndromic deafness type 13"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 13", "shortest_name_length": 6}
{"curie": "MONDO:0010472", "names": ["CDG1S", "DEE36", "CDGIs", "EIEE36", "CDG-Is", "CDG Is", "ALG13-CDG", "CDG syndrome type Is", "Early Infantile Epileptic Encephalopathy 36", "early infantile epileptic encephalopathy 36", "Congenital disorder of glycosylation type Is", "congenital disorder of glycosylation type 1s", "congenital disorder of glycosylation type Is", "Congenital disorder of glycosylation type 1s", "developmental and epileptic encephalopathy 36", "Developmental and Epileptic Encephalopathy 36", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 36", "epileptic encephalopathy, early infantile, 36", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Is", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 36", "congenital disorder of glycosylation, type Is", "developmental and epileptic encephalopathy, 36", "ALG13-CDG (congenital disorder of glycosylation)", "Congenital disorder of glycosylation type 1s (disorder)", "Congenital disorder of glycosylation type 1s (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 36", "shortest_name_length": 5}
{"curie": "UMLS:C3899648", "names": ["Childhood Paranasal Sinus Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Paranasal Sinus Carcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C0272230", "names": ["SCID due to absent ADA", "SCID due to absent adenosine deaminase", "severe combined immunodeficiency - adenosine deaminase deficiency", "severe combined immunodeficiency due to absent adenosine deaminase", "Severe combined immunodeficiency due to absent adenosine deaminase", "Severe combined immunodeficiency (SCID) due to absent adenosine deaminase", "Severe combined immunodeficiency due to absent adenosine deaminase (disorder)", "severe combined immunodeficiency due to absent adenosine deaminase (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SCID due to absent adenosine deaminase", "shortest_name_length": 22}
{"curie": "MONDO:0019957", "names": ["PPoma", "pancreatic polypeptidoma", "Pancreatic polypeptidoma", "Pancreatic polypeptide-oma", "pancreatic polypeptide tumor", "Pancreatic Polypeptide Tumor", "pancreatic polypeptide neoplasm", "Pancreatic Polypeptide Neoplasm", "Pancreatic polypeptidoma (disorder)", "pancreatic multiple hormonal syndrome", "multiple hormonal syndrome, pancreatic", "interacinar cell pancreatic polypeptide tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PPoma", "shortest_name_length": 5}
{"curie": "UMLS:C1332067", "names": ["AJCC G2 Sarcoma", "AJCC Grade 2 Sarcoma", "AJCC Grade II Sarcoma", "Moderately Differentiated Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AJCC Grade 2 Sarcoma", "shortest_name_length": 15}
{"curie": "UMLS:C3897515", "names": ["Stage IVB Sinonasal Squamous Cell Carcinoma AJCC v7", "Stage IVB Nasal Cavity and Paranasal Sinus Squamous Cell Cancer", "Stage IVB Nasal Cavity and Paranasal Sinus Squamous Cell Carcinoma", "Stage IVB Nasal Cavity and Paranasal Sinus Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Sinonasal Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 51}
{"curie": "UMLS:C1335323", "names": ["Papillary Breast Hyperplasia", "Papillary Hyperplasia of Breast", "Papillary Hyperplasia of the Breast", "Papillary Ductal Breast Hyperplasia", "Breast Papillary Ductal Hyperplasia", "Papillary Duct Hyperplasia of Breast", "Papillary Duct Hyperplasia of the Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Papillary Ductal Hyperplasia", "shortest_name_length": 28}
{"curie": "UMLS:C0000925", "names": ["cut", "Cut", "cuts", "cut wound", "Cut wound", "Incised wound", "incised wound", "Wound, incised", "Incised wound, NOS", "Incised wound (disorder)", "Incised wound - morphology", "Incised wound - morphology (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Incised wound", "shortest_name_length": 3}
{"curie": "MONDO:0023682", "names": ["Tympanic nerve tumor", "Tympanic nerve tumour", "Tympanic nerve tumors", "tympanic paraganglioma", "Tympanic paraganglioma", "Tympanic Paraganglioma", "Tympanic nerve tumours", "Glomus tympanicum tumor", "Glomus Tympanicum Tumor", "GLOMUS TYMPANICUM TUMOR", "Tumor, Glomus Tympanicum", "Glomus Tympanicum Tumors", "Glomus tympanicum tumour", "GLOMEROCYTOMA TYMPANICUM", "Tumors, Glomus Tympanicum", "glomus tympanicum neoplasm", "Glomus tympanicum paraganglioma", "Glomus tympanicum tumor (disorder)", "glomus tympanicum neoplasm (diagnosis)", "Tympanic nerve tumors (glomus tympanicum)", "neoplasm of paraganglioma extra-adrenal glomus tympanicum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tympanic paraganglioma", "shortest_name_length": 20}
{"curie": "MONDO:0800148", "names": ["autoinflammatory syndrome due to TBK1 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoinflammatory syndrome due to TBK1 deficiency", "shortest_name_length": 48}
{"curie": "UMLS:C4525400", "names": ["IIIB", "stage IIIB distal bile duct cancer", "stage IIIB distal bile duct cancer AJCC v7", "Stage IIIB Distal Bile Duct Cancer AJCC v8", "Stage IIIB Distal Bile Duct Carcinoma AJCC v8", "stage IIIB extrahepatic distal bile duct cancer", "Stage IIIB Extrahepatic (Distal) Bile Duct Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Distal Bile Duct Cancer AJCC v8", "shortest_name_length": 4}
{"curie": "MONDO:0035682", "names": ["FD/MAS spectrum", "FD/MAS syndrome", "Fibrous dysplasia/McCune-Albright spectrum", "fibrous dysplasia/McCune-Albright syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibrous dysplasia/McCune-Albright syndrome", "shortest_name_length": 15}
{"curie": "UMLS:C4054734", "names": ["Incontinent Epispadias"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Incontinent Epispadias", "shortest_name_length": 22}
{"curie": "MONDO:0021446", "names": ["Benign Epiglottic Tumor", "Benign Epiglottis Tumor", "benign epiglottic tumor", "benign Epiglottis tumor", "Benign Tumor of Epiglottis", "benign tumor of Epiglottis", "benign Epiglottis neoplasm", "benign epiglottic neoplasm", "epiglottis benign neoplasm", "Benign Epiglottic Neoplasm", "Benign Epiglottis Neoplasm", "benign neoplasm of epiglottis", "Benign Neoplasm of Epiglottis", "Benign neoplasm of epiglottis", "Benign Tumor of the Epiglottis", "benign tumor of the Epiglottis", "benign neoplasm of the Epiglottis", "Benign neoplasm of epiglottis NOS", "Benign Neoplasm of the Epiglottis", "Benign neoplasm of epiglottis, NOS", "Benign neoplasm of epiglottis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of epiglottis", "shortest_name_length": 23}
{"curie": "UMLS:C0086512", "names": ["Kock pouch", "Kock Pouch", "Pouch, Kock", "Continent ileostomy - stoma", "Continent ileostomy - stoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kock Pouch", "shortest_name_length": 10}
{"curie": "UMLS:C1513146", "names": ["Mesenteric EGIST", "Mesenteric Gastrointestinal Stromal Tumor", "Mesenteric Extragastrointestinal Stromal Tumor", "Mesenteric Gastrointestinal Stromal Tumor (GIST)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mesenteric Gastrointestinal Stromal Tumor", "shortest_name_length": 16}
{"curie": "MONDO:0001870", "names": ["GLOMERULONEPHRITIS POST STREPTOCOCCAL", "Post streptococcal glomerulonephritis", "poststreptococcal; glomerulonephritis", "post-streptococcal glomerulonephritis", "Post-Streptococcal Glomerulonephritis", "Post-streptococcal glomerulonephritis", "glomerulonephritis; poststreptococcal", "Acute Proliferative Glomerulonephritis", "GLOMERULONEPHRITIS, STREPTOCOCCAL, ACUTE", "acute poststreptococcal glomerulonephritis", "Acute poststreptococcal glomerulonephritis", "Acute post-streptococcal glomerulonephritis", "poststreptococcal; glomerulonephritis, acute", "PSGN - Post-streptococcal glomerulonephritis", "PSGN - post-streptococcal glomerulonephritis", "glomerulonephritis; poststreptococcal, acute", "Acute poststreptococcal glomerulonephritis syndrome", "acute poststreptococcal glomerulonephritis (diagnosis)", "Acute glomerulonephritis due to and following streptococcal infection", "Acute glomerulonephritis due to and following streptococcal infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute poststreptococcal glomerulonephritis", "shortest_name_length": 37}
{"curie": "UMLS:C1332047", "names": ["AIDS-Related Isosporiasis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Isosporiasis", "shortest_name_length": 25}
{"curie": "UMLS:C4289323", "names": ["FIGO Stage IC2 Ovarian Cancer", "FIGO Stage IC2 Ovarian Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Stage IC2 Ovarian Cancer", "shortest_name_length": 29}
{"curie": "MONDO:0004594", "names": ["Obstetric pulmonary embolus", "puerperal pulmonary embolism", "Puerperal pulmonary embolism", "Obstetric pulmonary embolism", "Obstetrical pulmonary embolism", "obstetrical pulmonary embolism", "Puerperal pulmonary embolism NOS", "Puerperal pulmonary embolism, NOS", "Puerperal (pulmonary) embolism NOS", "Obstetric (pulmonary) embolism NOS", "Obstetrical pulmonary embolism, NOS", "Obstetric pulmonary embolism (disorder)", "puerperal pulmonary embolism (diagnosis)", "obstetrical pulmonary embolism (diagnosis)", "Pulmonary embolism in pregnancy childbirth or puerperium, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "puerperal pulmonary embolism", "shortest_name_length": 27}
{"curie": "MONDO:0035474", "names": ["PIEZO1-related LRHF/GLD", "generalized lymphatic dysplasia of Fotiou", "PIEZO1-related lymphatic-related hydrops fetalis", "PIEZO1-related generalized lymphatic dysplasia with systemic involvement", "PIEZO1-related generalized lymphatic dysplasia with non-immune hydrops fetalis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PIEZO1-related generalized lymphatic dysplasia with non-immune hydrops fetalis", "shortest_name_length": 23}
{"curie": "MONDO:0023569", "names": ["Kozlowski Ouvrier syndrome", "Agenesis of the corpus callosum with mental retardation and osseous lesions", "agenesis of the corpus callosum with mental retardation and osseous lesions", "agenesis of the corpus callosum with intellectual disability and osseous lesions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kozlowski Ouvrier syndrome", "shortest_name_length": 26}
{"curie": "MONDO:0004310", "names": ["adult ependymoblastoma", "Adult Ependymoblastoma", "ependymoblastoma, adult", "ependymoblastoma of adults", "Embryonal Tumor with Multilayered Rosettes, C19MC-Altered", "embryonal tumor with multilayered rosettes, C19MC-altered", "adult embryonal tumor with multilayered rosettes, C19MC-altered", "adult embryonal tumor with multilayered rosettes, c19mc-altered", "Adult Embryonal Tumor with Multilayered Rosettes, C19MC-Altered"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult embryonal tumor with multilayered rosettes, c19mc-altered", "shortest_name_length": 22}
{"curie": "UMLS:C0281709", "names": ["Recurrent Large Cell Lymphoma", "Relapsed Pediatric Large Cell Lymphoma", "Relapsed Childhood Large Cell Lymphoma", "relapsed pediatric large cell lymphoma", "relapsed childhood large cell lymphoma", "lymphoma, relapsed childhood large cell", "recurrent pediatric large cell lymphoma", "pediatric large cell lymphoma, relapsed", "Recurrent Pediatric Large Cell Lymphoma", "recurrent childhood large cell lymphoma", "relapsed large cell lymphoma, childhood", "Recurrent Childhood Large Cell Lymphoma", "childhood large cell lymphoma, relapsed", "childhood large cell lymphoma, recurrent", "pediatric large cell lymphoma, recurrent", "large cell lymphoma, childhood, relapsed", "lymphoma, recurrent childhood large cell", "recurrent large cell lymphoma, childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Large Cell Lymphoma", "shortest_name_length": 29}
{"curie": "MONDO:0003684", "names": ["Clear cell chondrosarcoma", "Clear Cell Chondrosarcoma", "clear cell chondrosarcoma", "Clear Cell Chondrosarcomas", "Chondrosarcoma, Clear Cell", "Chondrosarcomas, Clear Cell", "clear cell chondrosarcoma (morphologic abnormality)", "Clear cell chondrosarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "clear cell chondrosarcoma", "shortest_name_length": 25}
{"curie": "EFO:0005524", "names": ["large artery stroke"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "large artery stroke", "shortest_name_length": 19}
{"curie": "UMLS:C1274301", "names": ["Benign Lymph Vessel Tumor", "Benign Tumor of Lymph Vessel", "Benign Lymph Vessel Neoplasm", "Benign Lymphatic Vessel Tumor", "Benign Neoplasm of Lymph Vessel", "Benign Tumor of the Lymph Vessel", "Benign neoplasm of lymph vessels", "Benign Lymphatic Vessel Neoplasm", "Benign Tumor of Lymphatic Vessel", "Benign Neoplasm of Lymphatic Vessel", "Benign Neoplasm of the Lymph Vessel", "Benign Tumor of the Lymphatic Vessel", "Benign Neoplasm of the Lymphatic Vessel", "Benign neoplasm of lymph vessels (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign neoplasm of lymph vessels", "shortest_name_length": 25}
{"curie": "UMLS:C5419073", "names": ["Recurrent Lung Non-Small Cell Squamous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Lung Non-Small Cell Squamous Carcinoma", "shortest_name_length": 48}
{"curie": "MONDO:0015285", "names": ["CAR", "CNC", "LAMB", "lamb", "NAME SYNDROME", "NAME syndrome", "NAME Syndrome", "LAMB Syndrome", "LAMB syndrome", "lamb syndrome", "LAMB SYNDROME", "LAMB Syndromes", "Carney complex", "Syndrome, LAMB", "CARNEY COMPLEX", "NAME Syndromes", "Carney Complex", "Syndromes, LAMB", "Carney Syndrome", "Complex, Carney", "Carney syndrome", "CARNEY SYNDROME", "Syndrome, Carney", "Carney's syndrome", "Carney's Syndrome", "Carney Complex, Type 1", "Carney Complex, type 2", "Carney complex variant", "Carney Complex, type 1", "Carney Complex, Type 2", "Carney complex (disorder)", "Carney complex (diagnosis)", "atrial myxoma with lentigines", "Atrial myxoma with lentigines", "Atrial Myxoma with Lentigines", "Carney complex, types I and II", "Carney Myxoma-Endocrine Complex", "CARNEY MYXOMA-ENDOCRINE COMPLEX", "Carney Myxoma Endocrine Complex", "Complex, Carney Myxoma-Endocrine", "Myxoma-Endocrine Complex, Carney", "Atrial myxoma with lentigines (diagnosis)", "Nevi, atrial myxoma, skin myxoma, ephelides syndrome", "LAMB (lentigines, atrial myxoma, blue nevi) syndrome", "nevi, atrial myxoma, skin myxoma, ephelides syndrome", "Nevi, Atrial Myxoma, Skin Myxoma, Ephelides Syndrome", "LAMB (lentigines, atrial myxoma, blue naevi) syndrome", "Naevi, atrial myxoma, skin myxoma, ephelides syndrome", "Myxoma - spotty pigmentation - endocrine overactivity", "MYXOMA, SPOTTY PIGMENTATION, AND ENDOCRINE OVERACTIVITY", "Myxoma, Spotty Pigmentation, and Endocrine Overactivity", "Myxoma-spotty pigmentation-endocrine overactivity syndrome", "NAME - Nevi, atrial myxoma, skin myxoma, ephelides syndrome", "NAME - Naevi, atrial myxoma, skin myxoma, ephelides syndrome", "Myxoma, spotty pigmentation, endocrine overactivity syndrome", "Lentigines, Atrial Myxoma, Mucocutaneous Myoma, Blue Nevus Syndrome", "Lentigines, atrial myxoma, mucocutaneous myoma, blue nevus syndrome", "lentigines, atrial myxoma, mucocutaneous myoma, blue Nevus syndrome", "Lentigines, atrial myxoma, mucocutaneous myoma, blue naevus syndrome", "LAMB - Lentigines, atrial myxoma, mucocutaneous myoma, blue nevus syndrome", "LAMB - Lentigines, Atrial Myxoma, Mucocutaneous Myoma, Blue Nevus Syndrome", "LAMB - Lentigines, atrial myxoma, mucocutaneous myoma, blue naevus syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carney complex", "shortest_name_length": 3}
{"curie": "MONDO:0001561", "names": ["GOO", "pyloric stenosi", "Stenosis pyloric", "Pyloric Stenosis", "pyloric stenoses", "pyloric stenosis", "Pyloric stenosis", "Pylorus stenosis", "PYLORIC STENOSIS", "STENOSIS PYLORIC", "stenosis; pylorus", "Stenosis, Pyloric", "PYLORIC STRICTURE", "Pylorus--Stenosis", "pylorus; stenosis", "stricture; pylorus", "pylorus; stricture", "Pylorus Obstruction", "Obstruction pyloric", "OBSTRUCTION PYLORIC", "Pyloric obstruction", "Pyloric Obstruction", "pyloric obstruction", "PYLORIC OBSTRUCTION", "Obstruction, Pyloric", "Pylorus Obstructions", "Obstruction, Pylorus", "Pyloric Obstructions", "Pyloric stenosis NOS", "PS - Pyloric stenosis", "Gastric outlet obstruction", "pyloric stenosis (disease)", "gastric outlet obstruction", "Gastric Outlet Obstruction", "GASTRIC OUTLET OBSTRUCTION", "obstruction; gastric outlet", "Gastric Outlet Obstructions", "Outlet Obstruction, Gastric", "Pyloric stenosis (disorder)", "GASTRIC OUT LET OBSTRUCTION", "gastric outflow obstruction", "Obstruction, Gastric Outlet", "Gastric outflow obstruction", "gastric outlet; obstruction", "pyloric stenosis (diagnosis)", "Outlet Obstructions, Gastric", "Obstructions, Gastric Outlet", "Pyloric obstruction (disorder)", "gastric outlet obstruction (diagnosis)", "Infantile hypertrophic pyloric stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyloric stenosis", "shortest_name_length": 3}
{"curie": "UMLS:C1332345", "names": ["AAH", "Atypical Alveolar Hyperplasia", "Bronchioloalveolar Cell Adenoma", "Atypical Adenomatous Lung Hyperplasia", "Atypical Adenomatous Hyperplasia of Lung", "Atypical Adenomatous Hyperplasia of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypical Adenomatous Lung Hyperplasia", "shortest_name_length": 3}
{"curie": "UMLS:C0751891", "names": ["Hypertensive Intracranial Hemorrhage", "Intracranial Hypertensive Hemorrhage", "Intracranial Hypertensive Hemorrhages", "Hemorrhage, Intracranial Hypertensive", "Intracranial Hemorrhage, Hypertensive", "Hemorrhage, Hypertensive Intracranial", "Hypertensive Intracranial Hemorrhages", "Hypertensive Hemorrhage, Intracranial", "Hypertensive Hemorrhages, Intracranial", "Hemorrhages, Hypertensive Intracranial", "Intracranial Hemorrhages, Hypertensive", "Hemorrhages, Intracranial Hypertensive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intracranial Hemorrhage, Hypertensive", "shortest_name_length": 36}
{"curie": "MONDO:0032641", "names": ["MRMV4", "MIRROR MOVEMENTS 4", "mirror movements 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mirror movements 4", "shortest_name_length": 5}
{"curie": "UMLS:C4682635", "names": ["Primary Peritoneal Cancer by AJCC v7 Stage", "Primary Peritoneal Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Peritoneal Cancer by AJCC v7 Stage", "shortest_name_length": 42}
{"curie": "UMLS:C1336137", "names": ["Stage IB Lung Adenocarcinoma", "Stage IB Adenocarcinoma of Lung", "Stage IB Adenocarcinoma of the Lung", "Stage IB Lung Adenocarcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Lung Adenocarcinoma AJCC v7", "shortest_name_length": 28}
{"curie": "UMLS:C0751586", "names": ["West Nile Fever Myelitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "West Nile Fever Myelitis", "shortest_name_length": 24}
{"curie": "UMLS:C4682754", "names": ["IIIC", "Stage IIIC Prostate Cancer", "stage IIIC prostate cancer", "Stage IIIC Prostate Cancer AJCC v8", "stage IIIC prostate cancer AJCC v8", "Stage IIIC Prostate Carcinoma AJCC v8", "stage IIIC prostate carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Prostate Cancer AJCC v8", "shortest_name_length": 4}
{"curie": "MONDO:0020384", "names": ["Niemann-Pick disease type E"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Niemann-Pick disease type E", "shortest_name_length": 27}
{"curie": "MONDO:0018102", "names": ["cornea dystrophy", "Corneal Dystrophy", "cornea; dystrophy", "Dystrophy, cornea", "CORNEAL DYSTROPHY", "dystrophy corneal", "dystrophy; cornea", "corneal dystrophy", "Corneal dystrophy", "cornea dystrophies", "Dystrophy, Corneal", "Corneal Dystrophies", "corneal dystrophies", "Corneal dystrophy, NOS", "corneal dystrophy (disease)", "Hereditary Corneal Dystrophy", "Corneal dystrophy (disorder)", "Hereditary corneal dystrophy", "Corneal Dystrophy, Hereditary", "corneal dystrophy (diagnosis)", "Dystrophy, Hereditary Corneal", "Hereditary Corneal Dystrophies", "Hereditary corneal dystrophies", "Corneal Dystrophies, Hereditary", "Hereditary corneal dystrophy, NOS", "corneal dystrophy (physical finding)", "Hereditary corneal dystrophy (disorder)", "Hereditary corneal dystrophy, unspecified", "Unspecified hereditary corneal dystrophies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal dystrophy", "shortest_name_length": 16}
{"curie": "MONDO:0017973", "names": ["non-classic congenital lipoid adrenal hyperplasia due to STAR deficency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-classic congenital lipoid adrenal hyperplasia due to STAR deficency", "shortest_name_length": 71}
{"curie": "MONDO:0014177", "names": ["MYP22", "MYOPIA 22, AUTOSOMAL DOMINANT", "myopia 22, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopia 22, autosomal dominant", "shortest_name_length": 5}
{"curie": "MONDO:0019676", "names": ["Type B brachydactyly", "Brachydactyly type B", "brachydactyly type B", "Brachydactyly syndrome type B", "Brachydactyly syndrome type B (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly type B", "shortest_name_length": 20}
{"curie": "UMLS:C1608389", "names": ["Autoimmune myocarditis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Autoimmune myocarditis", "shortest_name_length": 22}
{"curie": "UMLS:C0521494", "names": ["Application site pigmentation changes", "Application site pigmentation changes (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Application site pigmentation changes", "shortest_name_length": 37}
{"curie": "MONDO:0003318", "names": ["Mixed cell type Wilms tumor", "mixed cell type Wilms tumor", "Mixed Cell Type Wilms Tumor", "mixed cell type Wilms' tumor", "Wilms tumor, mixed cell type", "mixed cell type Wilm's tumor", "Wilms' tumor, mixed cell type", "Wilm's tumor, mixed cell type", "mixed cell type nephroblastoma", "Mixed Cell Type Nephroblastoma", "Mixed Cell Type Renal Wilms Tumor", "mixed cell type renal Wilms tumor", "mixed cell type renal adenosarcoma", "Mixed Cell Type Renal Wilm's Tumor", "mixed cell type renal Wilms' tumor", "Mixed Cell Type Renal Wilms' Tumor", "Mixed Cell Type Renal Adenosarcoma", "Mixed Cell Type Kidney Wilms Tumor", "mixed cell type renal Wilm's tumor", "mixed cell type kidney Wilms tumor", "mixed cell type renal Wilms tumour", "Mixed Cell Type Kidney Adenosarcoma", "mixed cell type kidney adenosarcoma", "mixed cell type kidney Wilms' tumor", "mixed cell type kidney Wilms' tumour", "Mixed Cell Type Kidney Nephroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed cell type kidney Wilms' tumor", "shortest_name_length": 27}
{"curie": "MONDO:0011041", "names": ["ECTODERMAL DYSPLASIA, HAIR/TOOTH TYPE", "ectodermal dysplasia, hair/Tooth type", "ectodermal dysplasia with natal teeth Turnpenny type", "Ectodermal dysplasia with natal teeth Turnpenny type", "Ectodermal Dysplasia with Natal Teeth, Turnpenny Type", "Ectodermal dysplasia with natal teeth, Turnpenny type", "ectodermal dysplasia with natal teeth, Turnpenny type", "ECTODERMAL DYSPLASIA WITH NATAL TEETH, TURNPENNY TYPE", "Ectodermal dysplasia with natal teeth Turnpenny type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia with natal teeth, Turnpenny type", "shortest_name_length": 37}
{"curie": "MONDO:0008783", "names": ["tgd", "FHD", "FHA", "TGD", "HDLD", "HDLC", "HDLDT1", "Tangier", "Tangier Disease", "TANGIER DISEASE", "tangier disease", "Tangier disease", "disease tangiers", "Tangier; disease", "diseases tangiers", "Analphaliproteinemia", "Analphaliproteinaemia", "analphalipoproteinemia", "ANALPHALIPOPROTEINEMIA", "Analphalipoproteinemia", "familial HDL deficiency", "Analphalipoproteinemias", "Familial HDL deficiency", "Analphalipoproteinaemia", "Analphalipo-proteinemia", "FAMILIAL HDL DEFICIENCY", "Cholesterol Thesaurismosis", "Tangier disease (disorder)", "Cholesterol thesaurismosis", "Tangier Disease Neuropathy", "Cholesterol Thesaurismoses", "cholesterol thesaurismosis", "HDL CHOLESTEROL, LOW SERUM", "Thesaurismosis, Cholesterol", "Thesaurismoses, Cholesterol", "Tangier disease (diagnosis)", "ALPHA LIPOPROTEIN DEFICIENCY", "alpha lipoprotein deficiency", "Neuropathy of Tangier Disease", "A-alphalipoprotein Neuropathy", "Tangier Hereditary Neuropathy", "A-alphalipoprotein neuropathy", "disease (or disorder); Tangier", "Neuropathy, A-alphalipoprotein", "Alphalipoproteinemia neuropathy", "A-alphalipoprotein Neuropathies", "Neuropathies, A-alphalipoprotein", "Alphalipoproteinaemia neuropathy", "Familial Hypoalphalipoproteinemia", "Familial hypoalphalipoproteinemia", "Hypoalphalipoproteinemia, Primary", "Primary Hypoalphalipoproteinemias", "HDL lipoprotein deficiency disease", "Familial Hypoalphalipoproteinemias", "Hypoalphalipoproteinemia, Familial", "HDL Lipoprotein Deficiency Disease", "Hypoalphalipoproteinemias, Primary", "HYPOALPHALIPOPROTEINEMIA, FAMILIAL", "familial Hypoalphalipo-proteinemia", "Familial hypoalphalipoproteinaemia", "A - alphalipoproteinemia neuropathy", "HIGH DENSITY LIPOPROTEIN DEFICIENCY", "Hypoalphalipoproteinemias, Familial", "A - alphalipoproteinaemia neuropathy", "familial alpha-lipoprotein deficiency", "Familial high density lipoprotein syndrome", "High Density Lipoprotein Deficiency, Type 1", "High-Density Lipoprotein Deficiency, Type I", "High Density Lipoprotein Deficiency, Type I", "high density lipoprotein deficiency, type 1", "HIGH DENSITY LIPOPROTEIN DEFICIENCY, TYPE 1", "LIPOPROTEIN DEFICIENCY, ALPHA, HIGH-DENSITY", "Familial high density lipoprotein deficiency", "familial high density lipoprotein deficiency", "Familial hypoalphalipoproteinemia (disorder)", "Familial alpha-Lipoprotein Deficiency Disease", "Lipoprotein Deficiency Disease, HDL, Familial", "Familial alpha Lipoprotein Deficiency Disease", "alpha-Lipoprotein Deficiency Disease, Familial", "ATP-binding cassette transporter A1 deficiency", "alpha Lipoprotein Deficiency Disease, Familial", "High-Density Lipoprotein Deficiency, Tangier Type", "high density lipoprotein deficiency, Tangier type", "Alpha high density lipoprotein deficiency disease", "HIGH DENSITY LIPOPROTEIN DEFICIENCY, TANGIER TYPE", "Alpha High Density Lipoprotein Deficiency Disease", "High Density Lipoprotein Deficiency, Tangier Type", "Familial High-Density Lipoprotein Deficiency Disease", "Familial High Density Lipoprotein Deficiency Disease", "familial high density lipoprotein deficiency disease", "High-Density Lipoprotein Deficiency Disease, Familial", "High Density Lipoprotein Deficiency Disease, Familial", "defective adenosine triphosphate-binding cassette transporter A1", "Defective adenosine triphosphate-binding cassette transporter A1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tangier disease", "shortest_name_length": 3}
{"curie": "MONDO:0003868", "names": ["Anterior Foramen Magnum Meningioma", "anterior foramen magnum meningioma", "Meningioma of Anterior Foramen Magnum", "meningioma of anterior Foramen magnum", "meningioma of the anterior Foramen magnum", "meningioma of the Anterior Foramen Magnum", "Meningioma of the Anterior Foramen Magnum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anterior foramen magnum meningioma", "shortest_name_length": 34}
{"curie": "UMLS:C3495832", "names": ["Rheumatic disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rheumatic disorder", "shortest_name_length": 18}
{"curie": "MONDO:0006545", "names": ["EM", "Target lesion", "erythema multiforme", "Erythema;multiforme", "erythema polymorphe", "Erythema polymorphe", "Erythema Multiforme", "multiforme erythema", "Erythema multiforme", "ERYTHEMA MULTIFORME", "erythema; multiforme", "erythema multiformes", "Erythaema polymorphe", "multiforme; erythema", "Oral erythema multiforme", "EM - Erythema multiforme", "Erythema multiforme, NOS", "erythema multiforme bullosum", "febrile mucocutaneous syndrome", "Erythema multiforme (disorder)", "erythema multiforme (diagnosis)", "Erythema multiforme, unspecified", "Herpes iris, erythema multiforme type", "Dermatostomatitis, erythema multiforme type", "erythema polymorphe, erythema multiforme type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythema multiforme", "shortest_name_length": 2}
{"curie": "MONDO:0024388", "names": ["Clostridiosis", "clostridia infection", "clostridial infection", "Clostridial infection", "Clostridium infection", "Clostridium Infection", "Clostridia infections", "Infection, Clostridium", "Clostridium Infections", "infection, Clostridium", "clostridial infections", "CLOSTRIDIAL INFECTIONS", "infections, Clostridium", "Infections, Clostridium", "Clostridial infection NOS", "Clostridial infection, NOS", "Clostridium infectious disease", "commensal Clostridium infection", "commensal infection, Clostridium", "Clostridial infection (disorder)", "commensal infections, Clostridium", "commensal Clostridium infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clostridium infectious disease", "shortest_name_length": 13}
{"curie": "MONDO:0007408", "names": ["Cryptotia, Familial", "CRYPTOTIA, FAMILIAL", "cryptotia, familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cryptotia, familial", "shortest_name_length": 19}
{"curie": "UMLS:C4525351", "names": ["IB", "Stage IB Intrahepatic Cholangiocarcinoma AJCC v8", "Stage IB Intrahepatic Bile Duct Cancer (Cholangiocarcinoma)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Intrahepatic Cholangiocarcinoma AJCC v8", "shortest_name_length": 2}
{"curie": "UMLS:C2983724", "names": ["Sinonasal Cancer by AJCC v6 Stage", "Sinonasal Carcinoma by AJCC v6 Stage", "Nasal Cavity and Paranasal Sinus Cancer by AJCC v6 Stage", "Nasal Cavity and Paranasal Sinus Carcinoma by AJCC v6 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Cancer by AJCC v6 Stage", "shortest_name_length": 33}
{"curie": "MONDO:0015272", "names": ["Camptodactyly taurinuria", "camptodactyly taurinuria", "Camptodactyly with Taurinuria", "camptodactyly with taurinuria", "Camptodactyly taurinuria syndrome", "camptodactyly-taurinuria syndrome", "Camptodactyly-taurinuria syndrome", "Familial streblodactyly with amino-aciduria", "familial streblodactyly with amino-aciduria", "Camptodactyly taurinuria syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "camptodactyly-taurinuria syndrome", "shortest_name_length": 24}
{"curie": "UMLS:C3899383", "names": ["Dialysis Catheter Tunnel Infection", "Tunnel Infection Associated with Dialysis Access"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dialysis Catheter Tunnel Infection", "shortest_name_length": 34}
{"curie": "UMLS:C0854696", "names": ["Malignant melanoma in situ"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant melanoma in situ", "shortest_name_length": 26}
{"curie": "MONDO:0011558", "names": ["USH2C", "USH2B, FORMERLY", "Usher syndrome type 2C", "Usher Syndrome Type 2C", "Usher syndrome, type 2C", "Usher syndrome type IIC", "USHER syndrome, type IIC", "USHER SYNDROME, TYPE IIC", "Usher Syndrome, Type IIC", "Usher syndrome, type IIb", "USHER SYNDROME, TYPE IIB, FORMERLY", "Usher syndrome type 2C (diagnosis)", "Usher syndrome, type IIb, formerly", "USHER SYNDROME, TYPE IIC, GPR98/PDZD7 DIGENIC", "Usher syndrome, type IIc, Gpr98/Pdzd7, digenic", "USHER SYNDROME, TYPE IIC, GPR98/PDZD7, DIGENIC", "Usher syndrome, type 2C, autosomal recessive, digenic dominant", "Usher syndrome, type 2C, GPR98/PDZD7 digenic, autosomal recessive, digenic dominant", "Usher syndrome, type IIC, GPR98/PDZD7 digenic, autosomal recessive, digenic dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Usher syndrome type 2C", "shortest_name_length": 5}
{"curie": "MONDO:0013951", "names": ["Cgj", "CGJ", "CG14", "Cg14", "PBD12A", "peroxisome biogenesis disorder 12A", "PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)", "peroxisome biogenesis disorder 12A (Zellweger)", "PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP J", "peroxisome biogenesis disorder, complementation group J", "Peroxisome Biogenesis Disorder, Complementation Group J", "PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 14", "peroxisome biogenesis disorder, complementation group 14", "Peroxisome Biogenesis Disorder, Complementation Group 14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder 12A (Zellweger)", "shortest_name_length": 3}
{"curie": "MONDO:0014585", "names": ["CMS3C", "congenital myasthenic syndrome 3C", "congenital myasthenic syndrome type 3C", "congenital myasthenic syndrome 3C associated with acetylcholine receptor deficiency", "MYASTHENIC SYNDROME, CONGENITAL, 3C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY", "myasthenic syndrome, congenital, 3C, associated with acetylcholine receptor deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myasthenic syndrome 3C", "shortest_name_length": 5}
{"curie": "MONDO:0003172", "names": ["Glomeruloid hemangioma", "glomeruloid hemangioma", "Glomeruloid Hemangioma", "Glomeruloid haemangioma", "Glomeruloid hemangioma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glomeruloid hemangioma", "shortest_name_length": 22}
{"curie": "MONDO:0019189", "names": ["disorder of amino acid and organic acid metabolism", "Disorder of amino acid and organic acid metabolism", "disorder of amino acid and other organic acid metabolism", "Disorder of amino acid and other organic acid metabolism", "Disorder of amino acid and organic acid metabolism (disorder)", "inborn disorder of amino acid and other organic acid metabolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of amino acid and other organic acid metabolism", "shortest_name_length": 50}
{"curie": "MONDO:0018806", "names": ["PIHL", "primary hepatolithiasis", "primary intrahepatic lithiasis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary intrahepatic lithiasis", "shortest_name_length": 4}
{"curie": "UMLS:C3495811", "names": ["Neonatal behavioral syndrome", "Neonatal behavioural syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neonatal behavioral syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0013171", "names": ["PNPD", "NP deficiency", "PNP Deficiency", "PNP deficiency", "PNPase deficiency", "nucleoside phosphorylase deficiency", "deficiency of inosine phosphorylase", "Deficiency of inosine phosphorylase", "Nucleoside phosphorylase deficiency", "Nucleoside Phosphorylase Deficiency", "NUCLEOSIDE PHOSPHORYLASE DEFICIENCY", "NP - Nucleoside phosphorylase deficiency", "purine nucleoside phosphorylase deficiency", "Purine-nucleoside phosphorylase deficiency", "PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY", "purine-nucleoside phosphorylase deficiency", "Purine nucleoside phosphorylase deficiency", "Purine Nucleoside Phosphorylase Deficiency", "Purine-Nucleoside Phosphorylase deficiency", "Purine-Nucleoside Phosphorylase Deficiency", "purine nucleoside phosphorylase; deficiency", "deficiency; purine nucleoside phosphorylase", "Deficiency of purine-nucleoside phosphorylase", "purine nucleoside phosphorylase deficiency (PNP)", "Purine nucleoside phosphorylase [PNP] deficiency", "PNP - Purine nucleoside phosphorylase deficiency", "Purine-nucleoside phosphorylase deficiency (disorder)", "purine nucleoside phosphorylase deficiency (diagnosis)", "immunodeficiency due to purine nucleoside phosphorylase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "purine nucleoside phosphorylase deficiency", "shortest_name_length": 4}
{"curie": "UMLS:C4521869", "names": ["Stage III Ampulla of Vater Cancer", "Stage III Ampulla of Vater Cancer AJCC v8", "Stage III Ampulla of Vater Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Ampulla of Vater Cancer AJCC v8", "shortest_name_length": 33}
{"curie": "MONDO:0001627", "names": ["amentia", "Amentia", "AMENTIA", "DEMENTIA", "Amentias", "Dementia", "dementia", "Dementias", "dementias", "Dementia NOS", "Dementia, NOS", "Organic dementia", "dementia disorder", "dementia disorders", "dementia (disease)", "Dementia (disorder)", "Unspecified dementia", "Progressive dementia", "progressive dementia", "DEMENTIA PROGRESSIVE", "dementia progressive", "dementia (diagnosis)", "Dementia, unspecified", "Dementia, progressive", "Dementia, neurological", "dementia; progressive (etiology)", "Dementing neurological disease or syndrome", "Other specified senile psychotic conditions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dementia", "shortest_name_length": 7}
{"curie": "EFO:0005140", "names": ["autoimmune disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune disease", "shortest_name_length": 18}
{"curie": "MONDO:0021562", "names": ["omphalitis", "Omphalitis", "Umbilicitis", "Cord infected", "Omphalitis;newborn", "newborn omphalitis", "Umbilical infection", "neonatal omphalitis", "Neonatal omphalitis", "Omphalitis of newborn", "Omphalitis (disorder)", "omphalitis (diagnosis)", "Umbilical inflammation", "Infection of umbilicus", "Infection of navel cord", "Inflammation of umbilicus", "infection; navel, newborn", "Omphalitis of newborn NOS", "Omphalitis of the newborn", "navel; infection, newborn", "Infection of umbilical stump", "Umbilical cord stump infected", "Umbilical cord stump infection", "Umbilical infection of newborn", "neonatal omphalitis (diagnosis)", "Omphalitis of newborn (disorder)", "neonatal omphalitis of navel cord", "Umbilical stump infection of newborn", "Umbilical stump infection of the newborn", "neonatal omphalitis of navel cord (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "omphalitis", "shortest_name_length": 10}
{"curie": "MONDO:0018438", "names": ["EGID", "eosinophilic gastrointestinal disease", "primary eosinophilic gastrointestinal disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eosinophilic gastrointestinal disease", "shortest_name_length": 4}
{"curie": "MONDO:0010815", "names": ["SPONDYLOEPIPHYSEAL DYSPLASIA TARDA WITH CHARACTERISTIC FACIES", "spondyloepiphyseal dysplasia tarda with characteristic facies", "Spondyloepiphyseal Dysplasia Tarda with Characteristic Facies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepiphyseal dysplasia tarda with characteristic facies", "shortest_name_length": 61}
{"curie": "MONDO:0006611", "names": ["skin sarcoidosis", "sarcoidosis skin", "Skin sarcoidosis", "SARCOIDOSIS SKIN", "sarcoidosis; skin", "cutaneous sarcoid", "Cutaneous sarcoid", "skin; sarcoidosis", "Sarcoidosis of skin", "sarcoidosis of skin", "cutaneous sarcoidosis", "Sarcoidosis cutaneous", "Cutaneous sarcoidosis", "sarcoidosis cutaneous", "SARCOIDOSIS CUTANEOUS", "Cutaneous Sarcoidosis", "Sarcoidosis, cutaneous", "Skin sarcoidosis lesion", "zone of skin sarcoidosis", "lesions sarcoidosis skin", "sarcoidosis of zone of skin", "Cutaneous sarcoidosis (disorder)", "sarcoidosis with skin involvement", "sarcoidosis with skin involvement (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin sarcoidosis", "shortest_name_length": 16}
{"curie": "UMLS:C0475073", "names": ["SUBARACHNOID HEMORRHAGE TRAUMATIC", "Traumatic Subarachnoid Hemorrhage", "Traumatic subarachnoid hemorrhage", "Traumatic Subarachnoid Hemorrhages", "Subarachnoid Hemorrhage, Traumatic", "Traumatic subarachnoid haemorrhage", "Hemorrhage, Traumatic Subarachnoid", "hemorrhage; subarachnoid, traumatic", "Subarachnoid Hemorrhages, Traumatic", "subarachnoid; hemorrhage, traumatic", "Traumatic subarachnoid hemorrhage NOS", "Post Traumatic Subarachnoid Hemorrhage", "Post-Traumatic Subarachnoid Hemorrhage", "Subarachnoid Hemorrhage, Post-Traumatic", "Post-Traumatic Subarachnoid Hemorrhages", "Hemorrhage, Post-Traumatic Subarachnoid", "Subarachnoid hemorrhage following injury", "Hemorrhages, Post-Traumatic Subarachnoid", "Subarachnoid Hemorrhages, Post-Traumatic", "Traumatic cranial subarachnoid hemorrhage", "Subarachnoid haemorrhage following injury", "Traumatic cranial subarachnoid haemorrhage", "subarachnoid hemorrhage intracranial traumatic", "Traumatic intracranial subarachnoid hemorrhage", "traumatic subarachnoid intracranial hemorrhage", "Traumatic intracranial subarachnoid haemorrhage", "Subarachnoid hemorrhage due to traumatic injury", "Subarachnoid haemorrhage due to traumatic injury", "Traumatic hemorrhage into subarachnoid space of neuraxis", "Traumatic haemorrhage into subarachnoid space of neuraxis", "traumatic subarachnoid intracranial hemorrhage (diagnosis)", "Subarachnoid hemorrhage due to traumatic injury (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subarachnoid Hemorrhage, Traumatic", "shortest_name_length": 33}
{"curie": "UMLS:C0679403", "names": ["Vascular Stenosis", "stenosis vascular", "Vascular stenosis", "vascular stenosis", "vascular narrowing"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vascular stenosis", "shortest_name_length": 17}
{"curie": "MONDO:0006603", "names": ["Reactive Cutaneous Fibrous Lesion", "reactive cutaneous fibrous lesion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "reactive cutaneous fibrous lesion", "shortest_name_length": 33}
{"curie": "MONDO:0013114", "names": ["DFNA50", "autosomal dominant deafness 50", "DEAFNESS, AUTOSOMAL DOMINANT 50", "deafness, autosomal dominant 50", "deafness, autosomal dominant type 50", "autosomal dominant nonsyndromic deafness 50", "autosomal dominant nonsyndromic hearing loss 50", "autosomal dominant nonsyndromic deafness type 50"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 50", "shortest_name_length": 6}
{"curie": "MONDO:0021018", "names": ["LGMD1", "LGMD1E", "LGMD1D", "LGMDD1", "LGMD type 1D", "LGMD1D (DNAJB6)", "DNAJB6-related LGMD D1", "LGMD1E (Bushby and Beckmann, 2003)", "Limb girdle muscular dystrophy type 1", "Limb-girdle muscular dystrophy type 1D", "muscular dystrophy limb-girdle type 1D", "muscular dystrophy, limb-girdle type 1", "muscular dystrophy limb-girdle type 1E", "limb-girdle muscular dystrophy type 1D", "Muscular Dystrophy, Limb-Girdle, Type 1D", "muscular dystrophy, limb-girdle, type 1E", "muscular dystrophy, limb-girdle, type 1D", "DNAJB6-related limb-girdle muscular dystrophy D1", "muscular dystrophy, limb-girdle, type 1D, formerly", "muscular dystrophy, limb-girdle type 1 (diagnosis)", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 1", "muscular dystrophy, limb-girdle, autosomal dominant 1", "DNAJB6 autosomal dominant limb-girdle muscular dystrophy", "autosomal dominant limb-girdle muscular dystrophy type 1", "autosomal dominant limb-girdle muscular dystrophy type 1E", "autosomal dominant limb-girdle muscular dystrophy type 1D", "Autosomal dominant limb-girdle muscular dystrophy type 1D", "Autosomal dominant limb girdle muscular dystrophy type 1D", "autosomal dominant limb-girdle muscular dystrophy type 1D (DNAJB6)", "Autosomal dominant limb girdle muscular dystrophy type 1D (disorder)", "autosomal dominant limb-girdle muscular dystrophy caused by mutation in DNAJB6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant limb-girdle muscular dystrophy type 1D (DNAJB6)", "shortest_name_length": 5}
{"curie": "MONDO:0004129", "names": ["Anal Canal Carcinoma", "Cloacogenic Carcinoma", "Cloacogenic carcinoma", "CLOACOGENIC CARCINOMA", "cloacogenic carcinoma", "cloacogenic anal carcinoma", "Anal Cloacogenic Carcinoma", "Cloacogenic Anal Carcinoma", "Cloacogenic anal carcinoma", "anal cloacogenic carcinoma", "Anal Canal Cloacogenic Cancer", "Cloacogenic Carcinoma of Anus", "anal canal cloacogenic cancer", "cloacogenic carcinoma of anus", "anal canal cloacogenic carcinoma", "Anal Canal Cloacogenic Carcinoma", "Cloacogenic Carcinoma of the Anus", "cloacogenic carcinoma of the anus", "cloacogenic carcinoma (diagnosis)", "anal cancer, cloacogenic carcinoma", "anus cancer, cloacogenic carcinoma", "cloacogenic carcinoma of anal canal", "Anal Canal Transitional Zone Carcinoma", "cloacogenic carcinoma of anus (diagnosis)", "cloacogenic carcinoma (morphologic abnormality)", "Cloacogenic carcinoma (morphologic abnormality)", "cloacogenic carcinoma of anal canal (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cloacogenic carcinoma", "shortest_name_length": 20}
{"curie": "MONDO:0006284", "names": ["Major Salivary Gland Cancer", "major salivary gland cancer", "Major Salivary Gland Carcinoma", "major salivary gland carcinoma", "carcinoma of major salivary gland", "carcinoma of Major salivary gland", "Carcinoma of Major Salivary Gland", "carcinoma of the major salivary gland", "Carcinoma of the Major Salivary Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "major salivary gland carcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0030680", "names": ["CMD2F", "dilated cardiomyopathy 2F", "CARDIOMYOPATHY, DILATED, 2F", "cardiomyopathy, dilated, 2F"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiomyopathy, dilated, 2F", "shortest_name_length": 5}
{"curie": "MONDO:0017859", "names": ["colchicine toxicity", "colchicine poisoning", "Colchicine poisoning", "Poisoning by colchicine", "toxicity from colchicine", "Poisoning caused by colchicine", "colchicine toxicity (diagnosis)", "Poisoning caused by colchicine (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colchicine poisoning", "shortest_name_length": 19}
{"curie": "OMIM:612542", "names": ["B12QTL1", "VITAMIN B12 PLASMA LEVEL QUANTITATIVE TRAIT LOCUS 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 7}
{"curie": "UMLS:C1696946", "names": ["Polyomavirus-associated nephropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Polyomavirus-associated nephropathy", "shortest_name_length": 35}
{"curie": "MONDO:0008559", "names": ["THPH1", "Vein thrombosis", "vein thrombosis", "Phlebothrombosis", "PHLEBOTHROMBOSIS", "phlebothrombosis", "Phlebothromboses", "thrombosis venous", "Venous thrombosis", "Thrombosis venous", "Venous Thromboses", "venous thrombosis", "THROMBOSIS VENOUS", "venous thromboses", "Thrombosis;venous", "Venous Thrombosis", "VENOUS THROMBOSIS", "vein; clot (blood)", "clot (blood); vein", "Thromboses, Venous", "Blood clot in vein", "Thrombosis, Venous", "hyperprothrombinemia", "Venous thrombosis NOS", "Thrombosis (vein) NOS", "Phlebothrombosis, NOS", "Venous thromboembolism", "Venous thrombosis, NOS", "a blood clot in the vein", "prothrombin thrombophilia", "Venous thrombosis (disorder)", "venous thrombosis (diagnosis)", "thrombosis, protection against", "THROMBOSIS, PROTECTION AGAINST", "factor II-related thrombophilia", "prothrombin-related thrombophilia", "prothrombin G20210A thrombophilia", "prothrombin 20210G>A thrombophilia", "thromboembolism, susceptibility to", "thrombophilia due to thrombin defect", "THROMBOPHILIA DUE TO FACTOR 2 DEFECT", "thrombophilia due to Factor 2 defect", "THROMBOPHILIA DUE TO THROMBIN DEFECT", "thrombophilia due to factor 2 defect", "venous thrombosis, protection against", "thrombophilia 1 due to thrombin defect", "venous thromboembolism, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombophilia due to thrombin defect", "shortest_name_length": 5}
{"curie": "UMLS:C2987267", "names": ["Esophageal Synovial Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Synovial Sarcoma", "shortest_name_length": 27}
{"curie": "MONDO:0025956", "names": ["ovarian remnant syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian remnant syndrome", "shortest_name_length": 24}
{"curie": "UMLS:C4525621", "names": ["Stage I Ampulla of Vater Neuroendocrine Tumor", "Stage I Ampulla of Vater Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Ampulla of Vater Neuroendocrine Tumor AJCC v8", "shortest_name_length": 45}
{"curie": "UMLS:C4330340", "names": ["Hypogonadotropic Hypogonadism with Adrenal Hypoplasia Congenita"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypogonadotropic Hypogonadism with Adrenal Hypoplasia Congenita", "shortest_name_length": 63}
{"curie": "UMLS:C4316923", "names": ["Benign Osteoclastic Giant Cell-Rich Tumor of Bone", "Benign Osteoclastic Giant Cell-Rich Tumor of the Bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Osteoclastic Giant Cell-Rich Tumor of Bone", "shortest_name_length": 49}
{"curie": "MONDO:0006381", "names": ["Plexiform ameloblastoma", "plexiform ameloblastoma", "Plexiform Ameloblastoma", "Plexiform ameloblastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "plexiform ameloblastoma", "shortest_name_length": 23}
{"curie": "MONDO:0021380", "names": ["myocardial tumor", "myocardium tumor", "Myocardial Tumor", "myocardial neoplasm", "myocardium neoplasm", "tumor of myocardium", "Myocardial Neoplasm", "Tumor of Myocardium", "neoplasm of myocardium", "Neoplasm of myocardium", "Neoplasm of Myocardium", "Tumor of the Myocardium", "tumor of the myocardium", "Neoplasm of the Myocardium", "neoplasm of the myocardium", "myocardium neoplasm (disease)", "Neoplasm of myocardium (disorder)", "neoplasm of myocardium (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplasm of myocardium", "shortest_name_length": 16}
{"curie": "UMLS:C3160846", "names": ["Seizure like phenomena"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Seizure like phenomena", "shortest_name_length": 22}
{"curie": "MONDO:0006075", "names": ["myelolipoma", "Myelolipoma", "Myelolipomas", "myelolipomas", "MYELOLIPOMA, benign", "MYELOLIPOMA, BENIGN", "Adrenal myelolipoma", "Myelolipoma (disorder)", "Adrenal Gland Myelolipoma", "adrenal gland myelolipoma", "adipose tissue myelolipoma", "myelolipoma of fatty tissue", "Myelolipoma of adrenal gland", "Myelolipoma (morphologic abnormality)", "Myelolipoma of adrenal gland (disorder)", "myelolipoma of fatty tissue (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adrenal gland myelolipoma", "shortest_name_length": 11}
{"curie": "UMLS:C0278679", "names": ["Hypernephroma recurrent", "recurrent hypernephroma", "hypernephroma, recurrent", "Renal carcinoma recurrent", "Carcinoma kidney recurrent", "Kidney carcinoma recurrent", "cancer cell recurrent renal", "recurrent renal cell cancer", "Recurrent Renal Cell Cancer", "Relapsed Renal Cell Carcinoma", "Renal cell carcinoma recurrent", "recurrent renal cell carcinoma", "Recurrent Renal Cell Carcinoma", "renal cell carcinoma, recurrent", "Renal Cell Carcinoma, Recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal cell carcinoma recurrent", "shortest_name_length": 23}
{"curie": "UMLS:C4725951", "names": ["Metastatic Gastrointestinal Stromal Tumor", "Metastatic Gastrointestinal Stromal Tumor (GIST)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Gastrointestinal Stromal Tumor", "shortest_name_length": 41}
{"curie": "UMLS:C0279627", "names": ["adult AMML", "adult AMMoL", "Adult AMMoL", "AMML, adult", "AMMoL, adult", "M4 Adult Acute Leukemia", "Adult Acute M4 Leukemia", "adult acute M4 leukemia", "M4 leukemia, adult acute", "Acute Myelomonocytic Leukemia", "Adult Acute Myelomonocytic Leukemia", "myelomonocytic leukemia, adult acute", "acute myelomonocytic leukemia, adult", "leukemia, adult acute myelomonocytic", "adult acute myelomonoblastic leukemia", "M4 adult acute myelomonocytic leukemia", "M4 Adult Acute Myelomonocytic Leukemia", "myelomonoblastic leukemia, adult acute", "acute myelomonoblastic leukemia, adult", "Adult Acute Myelomonocytic Leukemia (M4)", "adult acute myelomonocytic leukemia (M4)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Acute Myelomonocytic Leukemia", "shortest_name_length": 10}
{"curie": "MONDO:0005765", "names": ["Aphthosis", "aphthosis", "Aphthus fever", "aphthous fever", "Aphthous fever", "FEVER, APHTHOUS", "fever; aphthous", "aphthous; fever", "Epizootic aphtae", "Epizootic aphthae", "EPIZOOTIC APHTHAE", "mouth disease foot", "mouth foot disease", "epizootic; aphthae", "aphthae; epizootic", "foot mouth disease", "disease foot mouth", "foot & mouth disease", "Epizootic stomatitis", "stomatitis; epizootic", "epizootic; stomatitis", "foot and mouth disease", "Foot and Mouth Disease", "hoof-and-mouth disease", "Hoof-and-mouth disease", "Foot-and-Mouth Disease", "disease foot and mouth", "disease foot-and-mouth", "foot-and-mouth disease", "Foot-and-mouth disease", "FOOT AND MOUTH DISEASE", "Foot and mouth disease", "Foot-and-Mouth Diseases", "Disease, Foot-and-Mouth", "Diseases, Foot-and-Mouth", "Foot-and-mouth disease (disorder)", "foot and mouth disease (diagnosis)", "disease (or disorder); foot and mouth disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "foot and mouth disease", "shortest_name_length": 9}
{"curie": "UMLS:C0919924", "names": ["pulmonary toxicity", "Pulmonary toxicity", "Pulmonary Toxicity", "Pulmonary toxicity NOS", "Drug-induced pulmonary toxicity", "Drug-induced pulmonary toxicity (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pulmonary toxicity", "shortest_name_length": 18}
{"curie": "MONDO:0019701", "names": ["CDP", "Stippled Epiphyses", "stippled epiphyses", "Stippled epiphyses", "dysplasia; punctata", "Epiphyses, Stippled", "Epiphyseal stippling", "Chondrodysplasia punctata", "chondrodysplasia punctata", "Chondrodysplasia Punctata", "Stippling of the epiphyses", "chondrodysplasia; punctata", "punctata; chondrodysplasia", "Chondrodysplasia calcificans", "dysplasia; epiphysis, punctata", "Chondrodysplasia punctata, NOS", "Dysplasia Epiphysialis Punctata", "Epiphyseal punctate calcifications", "chondrodysplasia punctata congenita", "Chondrodysplasia punctata congenita", "chondrodysplasia punctata (diagnosis)", "chondrodysplasia calcificans congenita", "Chondrodysplasia calcificans congenita", "Chondrodystrophia Calcificans Congenita", "calcificans congenita; chondrodysplasia", "chondrodysplasia; calcificans congenita", "epiphysis; dysplasia epiphysealis punctata", "Speckled calcifications in end part of bone", "Chondrodysplasia punctata congenita (disorder)", "Chondrodysplasia punctata (stippled epiphyses) group", "Chondrodysplasia Punctata (Stippled Epiphyses) Group", "chondrodysplasia punctata (stippled epiphyses) Group", "Chondrodysplasia punctata (stippled epiphyses) group (disorder)", "osteochondrodysplasia with defects of growth of tubular bones and spine chondrodysplasia punctata"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chondrodysplasia punctata", "shortest_name_length": 3}
{"curie": "MONDO:0006396", "names": ["rectal villous adenoma", "Rectal Villous Adenoma", "rectum villous adenoma", "Rectal villous adenoma", "Villous Adenoma of Rectum", "Villous adenoma of rectum", "villous adenoma of rectum", "Villous Adenoma of the Rectum", "villous adenoma of the rectum", "Villous adenoma of rectum (disorder)", "villous adenoma of rectum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rectal villous adenoma", "shortest_name_length": 22}
{"curie": "MONDO:0007276", "names": ["CES", "CAT EYE SYNDROME", "Inv dup(22)(q11)", "Cat-Eye Syndrome", "INV DUP(22)(q11)", "cat-eye syndrome", "Cat eye syndrome", "cat eye syndrome", "INV DUP(22)(Q11)", "Cat Eye syndrome", "Cat-eye syndrome", "CAT eye syndrome", "cats eye syndrome", "cat eye syndrome (CES)", "CES - Cat eye syndrome", "Schachenmann's syndrome", "schmid-fraccaro syndrome", "SCHMID-FRACCARO SYNDROME", "Schmid Fraccaro syndrome", "schmid fraccaro syndrome", "Schmid-Fraccaro syndrome", "cat-eye syndrome (Type I)", "Partial trisomy 6 syndrome", "Cat eye syndrome (disorder)", "coloboma-anal atresia syndrome", "chromosome 22 partial tetrasomy", "CHROMOSOME 22 PARTIAL TETRASOMY", "Chromosome 22 partial tetrasomy", "ocular coloboma-imperforate anus syndrome", "Chromosomal imbalance syndrome, pair 6, partial trisomy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cat-eye syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0032573", "names": ["BMFS5", "BONE MARROW FAILURE SYNDROME 5", "bone marrow failure syndrome 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bone marrow failure syndrome 5", "shortest_name_length": 5}
{"curie": "MONDO:0002311", "names": ["retinal vascular disease", "RETINAL VASCULAR DISORDER", "Disorder vascular retinal", "Retinal Vascular Disorder", "VASCULAR DISORDER RETINAL", "Retinal vascular disorder", "DISORDER VASCULAR RETINAL", "Vascular disorder retinal", "retinal vascular disorder", "vascular appearance; change", "retina circulation disorder", "change; vascular appearance", "RETINAL VASCULAR DISORDER NOS", "Retinal vascular disorder NOS", "retina; change, vascular appearance", "Retinal vascular disorder (disorder)", "retinal vascular disorder (diagnosis)", "Changes in retinal vascular appearance", "Changes in vascular appearance of retina", "changes in vascular appearance of retina", "changes in vascular appearance of retina (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal vascular disorder", "shortest_name_length": 24}
{"curie": "MONDO:0006797", "names": ["RETINOPATHY HYPERTENSIVE", "hypertensive retinopathy", "Retinopathy;hypertensive", "Hypertensive retinopathy", "retinopathy hypertensive", "Retinopathy hypertensive", "Hypertensive Retinopathy", "Retinopathy, Hypertensive", "Hypertensive Retinopathies", "Retinopathies, Hypertensive", "Hypertensive retinopathy (disorder)", "hypertensive retinopathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertensive retinopathy", "shortest_name_length": 24}
{"curie": "UMLS:C1697974", "names": ["Bladder anastomotic leak", "anastomotic leak bladder", "Bladder Anastomotic Leakage", "Bladder anastomotic leak (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder Anastomotic Leakage", "shortest_name_length": 24}
{"curie": "MONDO:0003049", "names": ["Ovarian Large Cell NEC", "ovarian large cell NEC", "ovary large cell neuroendocrine carcinoma", "ovarian large cell neuroendocrine carcinoma", "Ovarian Large Cell Neuroendocrine Carcinoma", "ovarian large-cell neuroendocrine carcinoma", "Large-Cell Neuroendocrine Carcinoma of Ovary", "large cell neuroendocrine carcinoma of ovary", "Large Cell Neuroendocrine Carcinoma of Ovary", "large-cell neuroendocrine carcinoma of ovary", "Large Cell Neuroendocrine Carcinoma of the Ovary", "Large-Cell Neuroendocrine Carcinoma of the Ovary", "large cell neuroendocrine carcinoma of the ovary", "large-cell neuroendocrine carcinoma of the ovary", "ovarian non-small-cell type neuroendocrine carcinoma", "Ovarian Non-Small-Cell Type Neuroendocrine Carcinoma", "Non-Small-Cell Type Neuroendocrine Carcinoma of Ovary", "Non-small-cell type neuroendocrine carcinoma of Ovary", "non-small-cell type neuroendocrine carcinoma of ovary", "large cell neuroendocrine carcinoma of ovary (diagnosis)", "non-small-cell type neuroendocrine carcinoma of the ovary", "Non-Small-Cell Type Neuroendocrine Carcinoma of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian large-cell neuroendocrine carcinoma", "shortest_name_length": 22}
{"curie": "UMLS:C0278761", "names": ["DML, adult", "adult DM lymphoma", "DM lymphoma, adult", "Diffuse Mixed Cell Lymphoma", "diffuse mixed lymphoma, adult", "adult diffuse mixed cell lymphoma", "Adult Diffuse Mixed Cell Lymphoma", "diffuse mixed cell lymphoma, adult", "mixed cell lymphoma, diffuse, adult", "lymphoma, diffuse mixed cell, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Diffuse Mixed Cell Lymphoma", "shortest_name_length": 10}
{"curie": "MONDO:0004087", "names": ["basaloid lung carcinoma", "Lung Basaloid Large Cell Carcinoma", "basaloid large cell lung carcinoma", "basaloid large cell carcinoma of the lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "basaloid large cell lung carcinoma", "shortest_name_length": 23}
{"curie": "UMLS:C0861148", "names": ["Proarrhythmia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Proarrhythmia", "shortest_name_length": 13}
{"curie": "MONDO:0013398", "names": ["ACNINV3", "acne inversa, familial, 3", "ACNE INVERSA, FAMILIAL, 3", "PSEN1 familial acne inversa", "acne inversa, familial, type 3", "familial acne inversa caused by mutation in PSEN1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acne inversa, familial, 3", "shortest_name_length": 7}
{"curie": "MONDO:0018281", "names": ["CMDH", "Congenital muscular dystrophy with hyperlaxity", "congenital muscular dystrophy with hyperlaxity", "Congenital muscular dystrophy with hyperlaxity (disorder)", "congenital muscular dystrophy with hyperlaxity (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital muscular dystrophy with hyperlaxity", "shortest_name_length": 4}
{"curie": "UMLS:C0751500", "names": ["Petrous Sinus Thrombophlebitis", "Thrombophlebitis, Petrous Sinus", "Sinus Thrombophlebitis, Petrous", "Petrous Sinus Thrombophlebitides", "Thrombophlebitides, Petrous Sinus", "Sinus Thrombophlebitides, Petrous"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Petrous Sinus Thrombophlebitis", "shortest_name_length": 30}
{"curie": "MONDO:0003980", "names": ["jugular foramen schwannoma", "Jugular Foramen Schwannoma", "Jugular Foramen Neurilemmoma", "jugular Foramen neurilemmoma", "schwannoma of jugular foramen", "Schwannoma of Jugular Foramen", "Neurilemmoma of Jugular Foramen", "neurilemmoma of jugular Foramen", "schwannoma of the jugular Foramen", "Schwannoma of the Jugular Foramen", "Neurilemmoma of the Jugular Foramen", "neurilemmoma of the jugular Foramen"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schwannoma of jugular foramen", "shortest_name_length": 26}
{"curie": "UMLS:C4329636", "names": ["Central Nervous System Mesenchymal Chondrosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Mesenchymal Chondrosarcoma", "shortest_name_length": 49}
{"curie": "UMLS:C1699739", "names": ["Intraoperative reproductive tract injury", "intraoperative reproductive tract injury", "Intraoperative Reproductive System Injury", "intraoperative reproductive tract injury (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraoperative Reproductive System Injury", "shortest_name_length": 40}
{"curie": "MONDO:0006948", "names": ["artery occlusion retinal", "OCCLUSION RETINAL ARTERY", "Retinal artery occlusion", "RETINAL ARTERY OCCLUSION", "retinal artery occlusion", "Retinal Artery Occlusion", "retina; occlusion artery", "Occlusion retinal artery", "occlusion; retina, artery", "Retinal Artery Occlusions", "occlusion; artery, retina", "retinal artery occlusions", "Occlusion, Retinal Artery", "Retinal arterial occlusion", "Occlusions, Retinal Artery", "RAO - Retinal artery occlusion", "artery; retina, occlusion artery", "artery; occlusion, artery, retinal", "Retinal artery occlusion (disorder)", "retinal artery occlusion (diagnosis)", "retinal artery occlusion (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal artery occlusion", "shortest_name_length": 24}
{"curie": "UMLS:C0877373", "names": ["Advanced cancer", "Advanced Cancer", "cancer advanced", "advanced cancer", "Advanced Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced cancer", "shortest_name_length": 15}
{"curie": "UMLS:C2902961", "names": ["page kidney", "Page Kidney", "Page kidney", "Renal compression", "page kidney (diagnosis)", "Hypertension due to compression of renal parenchyma", "Hypertension due to compression of renal parenchyma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Page kidney", "shortest_name_length": 11}
{"curie": "MONDO:0000108", "names": ["BACTEREMIA, RESISTANCE TO", "bacteremia, susceptibility"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bacteremia, susceptibility", "shortest_name_length": 25}
{"curie": "MONDO:0006436", "names": ["submandibular gland adenoid cystic carcinoma", "Submandibular Gland Adenoid Cystic Carcinoma", "Cancer of submandibular gland, adenoid cystic", "Adenoid cystic carcinoma of submandibular gland", "Adenoid Cystic Carcinoma of Submandibular Gland", "adenoid cystic carcinoma of submandibular gland", "Adenoid Cystic Carcinoma of the Submandibular Gland", "adenoid cystic carcinoma of the submandibular gland", "salivary gland carcinoma adenoid cystic submandibular", "Adenoid cystic carcinoma of submandibular gland (disorder)", "Adenoid cystic carcinoma of submandibular gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "submandibular gland adenoid cystic carcinoma", "shortest_name_length": 44}
{"curie": "MONDO:0018460", "names": ["Eales", "Eales disease", "disease eales", "eales' disease", "Eales' disease", "Eale's disease", "eale's disease", "perivasculitis; retina", "Retinal perivasculitis", "retinal perivasculitis", "Retinal, perivasculitis", "Eales' disease (disorder)", "Eales' disease (diagnosis)", "idiopathic retinal vasculitis", "Idiopathic retinal vasculitis", "Idiopathic retinal perivasculitis", "idiopathic retinal perivasculitis", "retinal perivasculitis (diagnosis)", "idiopathic obliterative vasculopathy", "Idiopathic obliterative vasculopathy", "Idiopathic recurrent vitreal hemorrhage", "idiopathic recurrent vitreal hemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eales disease", "shortest_name_length": 5}
{"curie": "UMLS:C0276931", "names": ["Schistosoma; bovis", "Infection by Schistosoma Bovis", "Infection by Schistosoma bovis", "Infection by Schistosoma, bovis", "schistosomiasis; Schistosoma bovis", "Infection caused by Schistosoma bovis", "schistosomiasis due to Schistosoma bovis", "Infection caused by Schistosoma bovis (disorder)", "schistosomiasis due to Schistosoma bovis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infection by Schistosoma bovis", "shortest_name_length": 18}
{"curie": "MONDO:0019439", "names": ["amyloidosis AA", "AA amyloidosis", "aa amyloidosis", "Reactive amyloidosis", "reactive amyloidosis", "amyloid A amyloidosis", "Amyloid A amyloidosis", "Secondary Amyloidosis", "secondary amyloidosis", "Secondary amyloidosis", "amyloidosis secondary", "Amyloidosis, secondary", "AMYLOIDOSIS, SECONDARY", "Inflammatory amyloidosis", "inflammatory amyloidosis", "serum amyloid A amyloidosis", "inflammation AA amyloidosis", "Reactive systemic amyloidosis", "Apo serum amyloid A amyloidosis", "Amyloid A amyloidosis (disorder)", "secondary amyloidosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AA amyloidosis", "shortest_name_length": 14}
{"curie": "UMLS:C5556340", "names": ["Recurrent Polymorphous Low-Grade Neuroepithelial Tumor of the Young", "Recurrent Polymorphous Low Grade Neuroepithelial Tumor of the Young"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Polymorphous Low Grade Neuroepithelial Tumor of the Young", "shortest_name_length": 67}
{"curie": "MONDO:0007809", "names": ["IHL", "Porcupine man", "PORCUPINE MAN", "porcupine Man", "Lambert type ichthyosis", "Ichthyosis Lambert type", "ichthyosis, Lambert type", "Ichthyosis, Lambert Type", "Ichthyosis hystrix gravior", "ICHTHYOSIS HYSTRIX GRAVIOR", "ichthyosis hystrix gravior", "ICHTHYOSIS HYSTRIX, LAMBERT TYPE", "ichthyosis histrix, Lambert type", "Ichthyosis hystrix gravior (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ichthyosis histrix, Lambert type", "shortest_name_length": 3}
{"curie": "MONDO:0043287", "names": ["SVCS", "SVC syndrome", "SVC SYNDROME", "SVC Syndrome", "svc syndrome", "SVC Syndromes", "Syndrome, SVC", "SVC Obstruction", "SVC obstruction", "svc obstruction", "Obstruction, SVC", "SVC Obstructions", "Cranial vena cava syndrome", "superior vena cava syndrome", "SUPERIOR VENA CAVA SYNDROME", "VENA CAVA SUPERIOR SYNDROME", "Superior vena cava syndrome", "Superior Vena Cava Syndrome", "vena cava superior syndrome", "Superior vena cava occlusion", "superior vena caval syndrome", "Superior vena caval syndrome", "Superior Vena Cava Occlusion", "cava superior syndromes vena", "superior vena cava thrombosis", "Superior vena cava obstruction", "Superior Vena Cava Obstruction", "SUPERIOR VENA CAVA OBSTRUCTION", "VENA CAVA SUPERIOR OBSTRUCTION", "superior vena cava obstruction", "caval obstruction superior vena", "Superior caval vein obstruction", "Superior vena caval obstruction", "VENA CAVA OBSTRUCTION, SUPERIOR", "Occlusion of superior vena cava", "superior vena caval obstruction", "Obstruction of superior vena cava", "SVC - Superior vena cava obstruction", "SVCO - Superior vena cava obstruction", "Obstruction of the superior vena cava", "Obstruction of the Superior Vena Cava", "Superior vena cava syndrome (disorder)", "superior vena cava syndrome (diagnosis)", "Occlusion of superior vena cava (disorder)", "Obstruction of superior vena cava (disorder)", "Obstruction of superior vena cava (diagnosis)", "vascular system disorders obstruction superior vena cava"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "superior vena cava syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0005518", "names": ["Pseudohermaphroditism", "PSEUDOHERMAPHRODITISM", "pseudohermaphroditism", "Pseudohermaphroditism NOS", "Pseudohermaphroditism syndrome", "Pseudohermaphroditism (disorder)", "pseudohermaphroditism (diagnosis)", "Pseudohermaphroditism, unspecified", "Dysgenetic pseudohermaphroditism syndrome", "Indeterminate sex and pseudohermaphroditism", "indeterminate sex and pseudohermaphroditism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudohermaphroditism", "shortest_name_length": 21}
{"curie": "MONDO:0020730", "names": ["CTS", "CTS1", "carpal tunnel syndrome", "carpal tunnel syndrome 1", "carpal tunnel syndrome, familial", "amyotrophy, thenar, of carpal origin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carpal tunnel syndrome 1", "shortest_name_length": 3}
{"curie": "UMLS:C4682630", "names": ["Fallopian Tube Cancer by AJCC v8 Stage", "Fallopian Tube Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fallopian Tube Cancer by AJCC v8 Stage", "shortest_name_length": 38}
{"curie": "MONDO:0013541", "names": ["CDCBM1", "complex cortical dysplasia with other brain malformations 1", "CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 1", "cortical dysplasia, complex, with other brain malformations 1", "TUBB3 complex cortical dysplasia with other brain malformations", "complex cortical dysplasia with other brain malformations type 1", "cortical dysplasia, Complex, with Other brain malformations type 1", "cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation", "complex cortical dysplasia with other brain malformations caused by mutation in TUBB3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complex cortical dysplasia with other brain malformations 1", "shortest_name_length": 6}
{"curie": "MONDO:0011501", "names": ["Suarez-Stickler syndrome", "cortical defects wormian bones and dentinogenesis imperfecta", "Cortical Defects, Wormian Bones, and Dentinogenesis Imperfecta", "cortical defects, WORMIAN bones, and dentinogenesis imperfecta", "CORTICAL DEFECTS, WORMIAN BONES, AND DENTINOGENESIS IMPERFECTA", "wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia", "shortest_name_length": 24}
{"curie": "UMLS:C0343205", "names": ["Lupus vasculitis", "vasculitis lupus", "lupus vasculitis", "Lupus vasculitis (disorder)", "lupus vasculitis (diagnosis)", "Vasculitis due to lupus erythematosus", "Lupus erythematosus-associated vasculitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lupus vasculitis", "shortest_name_length": 16}
{"curie": "UMLS:C0004063", "names": ["mug", "mugs", "Mugged", "MUGGED", "Assault", "ASSAULT", "assault", "assaults", "attacked", "Attacked", "[X]Mugged", "Assault(s)", "assault(s)", "[X]Assault", "[X]Attacked", "ASSAULT NOS", "Assault (event)", "Assault by unspecified means", "[X]Assault by unspecified means"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Assault", "shortest_name_length": 3}
{"curie": "MONDO:0013035", "names": ["OFD11", "Ofds 11", "OFDS XI", "OFD syndrome 11", "Gabrielli syndrome", "GABRIELLI SYNDROME", "Orofaciodigital syndrome 11", "OROFACIODIGITAL SYNDROME XI", "Orofaciodigital syndrome XI", "orofaciodigital syndrome XI", "orofaciodigital syndrome 11", "Oral-facial-digital syndrome 11", "oral facial digital syndrome 11", "orofaciodigital syndrome type XI", "Orofaciodigital syndrome type 11", "orofaciodigital syndrome type 11", "Oro-facial digital syndrome type 11", "oral-facial-digital syndrome type 11", "oral facial digital syndrome type 11", "Oral-facial-digital syndrome type 11", "Oral-Facial-Digital Syndrome, Type XI", "oral-Facial-digital syndrome, type 11", "ORAL-FACIAL-DIGITAL SYNDROME, TYPE XI", "Orofaciodigital syndrome Gabrielli type", "Orofaciodigital syndrome, Gabrielli type", "orofaciodigital syndrome, Gabrielli type", "Oral-facial-digital syndrome Gabrielli type", "oral-facial-digital syndrome, Gabrielli type", "Oral-facial-digital syndrome, Gabrielli type", "Oro-facial digital syndrome type 11 (disorder)", "oral-facial-digital syndrome type 11 (diagnosis)", "Oral-Facial-Digital Syndrome with Skeletal Anomalies", "oral-Facial-digital syndrome with skeletal anomalies", "ORAL-FACIAL-DIGITAL SYNDROME WITH SKELETAL ANOMALIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orofaciodigital syndrome XI", "shortest_name_length": 5}
{"curie": "MONDO:0009674", "names": ["muscular dystrophy, adult-onset, with leukoencephalopathy", "MUSCULAR DYSTROPHY, ADULT-ONSET, WITH LEUKOENCEPHALOPATHY", "Muscular Dystrophy, Adult-Onset, with Leukoencephalopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy, adult-onset, with leukoencephalopathy", "shortest_name_length": 57}
{"curie": "MONDO:0013637", "names": ["PBC5", "primary biliary cholangitis 5", "biliary cirrhosis, primary, 5", "BILIARY CIRRHOSIS, PRIMARY, 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary biliary cholangitis 5", "shortest_name_length": 4}
{"curie": "MONDO:0100079", "names": ["DEE6", "EIEE6", "Dravet syndrome", "epileptic encephalopathy, early infantile, 6", "developmental and epileptic encephalopathy, 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 6", "shortest_name_length": 4}
{"curie": "MONDO:0009642", "names": ["Mohr", "OFD2", "Ofds 2", "OFDS II", "mohr syndrome", "Mohr Syndrome", "MOHR SYNDROME", "MOHR syndrome", "Mohr syndrome", "Syndrome, Mohr", "OFD syndrome 2", "mohrs syndrome", "Mohr's syndrome", "mohr's syndrome", "OFD syndrome type II", "Mohr-Claussen syndrome", "Mohr syndrome (disorder)", "orofaciodigital syndrome 2", "Orofaciodigital Syndrome II", "OROFACIODIGITAL SYNDROME II", "orofaciodigital syndrome II", "digito-orofacial syndrome II", "Orofaciodigital Syndrome IIs", "Orofacial-digital syndrome II", "oral facial digital syndrome 2", "orofaciodigital syndrome type 2", "oral-facial-digital syndrome II", "Orofaciodigital syndrome type 2", "orofaciodigital syndrome type II", "orofaciodigital (OFD) syndrome II", "oral facial digital syndrome type 2", "Oral-facial-digital syndrome type 2", "oral-facial-digital syndrome type 2", "Oral-facial-digital syndrome type II", "oral-Facial-digital syndrome, type 2", "Oral Facial Digital Syndrome, Type II", "ORAL-FACIAL-DIGITAL SYNDROME, TYPE II", "Oral-Facial-Digital Syndrome, Type II", "OFD II - Orofacial-digital syndrome II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orofaciodigital syndrome type II", "shortest_name_length": 4}
{"curie": "MONDO:0019223", "names": ["disorder of fatty acid and ketone body metabolism", "disorder of fatty acid oxidation and ketone body metabolism", "inborn disorder of fatty acid oxidation and ketone body metabolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of fatty acid and ketone body metabolism", "shortest_name_length": 49}
{"curie": "MONDO:0021658", "names": ["angiectasia", "Angiectasis", "angiectasis", "ANGIECTASIS", "Angiectasia", "angiectasias", "angioectasia", "Angioectasia", "angioectasias", "hemangiectasia", "Hemangiectasia", "Hemangiectasis", "Hemangiectases", "Angiectasis, NOS", "VASCULAR ECTASIA", "vascular ectasia", "Vascular Ectasia", "Vascular ectasia", "Angiectasia, NOS", "ectasias vascular", "Phlebarteriectasis", "Phlebarteriectasia", "Hemangiectasis, NOS", "Hemangiectasia, NOS", "Vascular ectasia, NOS", "angiectasis (diagnosis)", "Angiectasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vascular ectasia", "shortest_name_length": 11}
{"curie": "UMLS:C5239294", "names": ["Locally Advanced Cholangiocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Cholangiocarcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C4727009", "names": ["Metastatic Pancreatic Neuroendocrine Cancer", "Metastatic Pancreatic Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Pancreatic Neuroendocrine Carcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0019472", "names": ["NKTCL", "T/NK-cell lymphoma", "NK/T-cell lymphoma", "Angiocentric lymphoma", "RETICULOSIS, MALIGNANT", "Angiocentric lymphomas", "reticulosis, malignant", "lethal midline granuloma", "Lethal midline granuloma", "Angiocentric lymphoma NOS", "Angiocentric T-Cell Lymphoma", "Angiocentric T-cell lymphoma", "angiocentric T-cell lymphoma", "lymphoma; angiocentric T-cell", "angiocentric T-cell; lymphoma", "Extranodal NK/T lymphoma-nasal", "lymphoma; T-cell, angiocentric", "T-cell; lymphoma, angiocentric", "Extranodal nasal NK/T cell lymphoma", "extranodal nasal NK/T cell lymphoma", "nasal T/natural killer-cell lymphoma", "Extranodal NK T Cell Lymphoma, Nasal", "Extranodal NK-T-Cell Lymphoma, Nasal", "Nasal T/natural killer-cell lymphoma", "Nasal Type Extranodal NK/T-Cell Lymphoma", "nasal type Extranodal NK/T-cell lymphoma", "nasal type extranodal NK/T-cell lymphoma", "NK/T-cell lymphoma, nasal and nasal-type", "Extranodal NK/T-Cell Lymphoma, Nasal Type", "Extranodal NK T Cell Lymphoma, Nasal Type", "Extranodal NK/T-cell lymphoma, nasal type", "Extranodal NK-T-Cell Lymphoma, Nasal Type", "extranodal NK/T-cell lymphoma of nasal cavity", "Extranodal NK-T-Cell Lymphoma, Nasal and Nasal-Type", "Extranodal NK T Cell Lymphoma, Nasal and Nasal Type", "Extranodal natural killer/T-cell lymphoma, nasal type", "extranodal NK/T-cell lymphoma of nasal cavity (diagnosis)", "Extranodal natural killer/T-cell lymphoma, nasal type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extranodal nasal NK/T cell lymphoma", "shortest_name_length": 5}
{"curie": "UMLS:C1262005", "names": ["Ischemic cerebral infarction", "ischemic cerebral infarction", "Ischaemic cerebral infarction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ischemic cerebral infarction", "shortest_name_length": 28}
{"curie": "MONDO:0036218", "names": ["Lethal 1p36.33 deletion syndrome", "lethal pontocerebellar hypoplasia-hypotonia-respiratory insufficiency syndrome due to biallelic deletions in the ATAD3 gene cluster"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal pontocerebellar hypoplasia-hypotonia-respiratory insufficiency syndrome due to biallelic deletions in the ATAD3 gene cluster", "shortest_name_length": 32}
{"curie": "UMLS:C1709467", "names": ["Parathyroid Gland Hamartoma", "Parathyroid Gland Lipoadenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parathyroid Gland Lipoadenoma", "shortest_name_length": 27}
{"curie": "MONDO:0011048", "names": ["Battaglia-Neri syndrome", "epilepsy - microcephaly - skeletal dysplasia", "epilepsy-microcephaly-skeletal dysplasia syndrome", "MENTAL RETARDATION, MICROCEPHALY, EPILEPSY, AND COARSE FACE", "Mental Retardation, Microcephaly, Epilepsy, And Coarse Face", "mental retardation, microcephaly, epilepsy, and coarse face", "intellectual disability, microcephaly, epilepsy, and coarse face"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy-microcephaly-skeletal dysplasia syndrome", "shortest_name_length": 23}
{"curie": "UMLS:C0854198", "names": ["Intra-abdominal metastases", "Metastases to abdominal cavity", "Metastases to the Abdominal Cavity", "Metastasis to the Abdominal Cavity", "Metastatic Tumor to the Abdominal Cavity", "Metastatic Neoplasm to the Abdominal Cavity", "Metastatic Malignant Neoplasm in the Abdominal Cavity", "Metastatic Malignant Neoplasm to the Abdominal Cavity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastases to abdominal cavity", "shortest_name_length": 26}
{"curie": "UMLS:C4724929", "names": ["Recurrent Grade 3a Follicular Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Grade 3a Follicular Lymphoma", "shortest_name_length": 38}
{"curie": "MONDO:0009127", "names": ["dwarfism, low-birth-weight type with unresponsiveness to growth hormone", "Dwarfism, Low-Birth-Weight Type, with Unresponsiveness to Growth Hormone", "DWARFISM, LOW-BIRTH-WEIGHT TYPE, WITH UNRESPONSIVENESS TO GROWTH HORMONE", "dwarfism, low-birth-weight type, with unresponsiveness to growth hormone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dwarfism, low-birth-weight type, with unresponsiveness to growth hormone", "shortest_name_length": 71}
{"curie": "UMLS:C1449718", "names": ["Endocrine Breast Disease", "Breast Disease, Endocrine", "Endocrine Breast Diseases", "Disease, Endocrine Breast", "Breast Diseases, Endocrine", "Diseases, Endocrine Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endocrine Breast Diseases", "shortest_name_length": 24}
{"curie": "MONDO:0032804", "names": ["ECTD15", "ectodermal dysplasia 15", "ECTODERMAL DYSPLASIA 15, HYPOHIDROTIC/HAIR TYPE", "ectodermal dysplasia 15, hypohidrotic/hair type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia 15, hypohidrotic/hair type", "shortest_name_length": 6}
{"curie": "MONDO:0011017", "names": ["NXD", "KWWH type I", "MAL DE NAXOS", "Mal de Naxos", "Mal De Naxos", "NAXOS disease", "NAXOS DISEASE", "Naxos disease", "Keratoderma with wooly hair type I", "Keratoderma with woolly hair type I", "keratoderma with woolly hair type I", "palmoplantar keratoderma with arrythmogenic cardiomyopathy", "keratosis palmoplantaris with arrythmogenic cardiomyopathy", "Palmoplantar keratoderma with arrythmogenic cardiomyopathy", "Keratosis palmoplantaris with arrythmogenic cardiomyopathy", "woolly hair palmoplantar keratoderma cardiac abnormalities", "keratosis palmoplantaris with arrhythmogenic cardiomyopathy", "Keratosis palmoplantaris with arrhythmogenic cardiomyopathy", "KERATOSIS PALMOPLANTARIS WITH ARRHYTHMOGENIC CARDIOMYOPATHY", "palmoplantar hyperkeratosis with arrythmogenic cardiomyopathy", "Palmoplantar hyperkeratosis with arrythmogenic cardiomyopathy", "Palmoplantar hyperkeratosis with arrhythmogenic cardiomyopathy", "Woolly hair, palmoplantar keratoderma, and cardiac abnormalities", "woolly hair, palmoplantar keratoderma, and Cardiac abnormalities", "WOOLLY HAIR, PALMOPLANTAR KERATODERMA, AND CARDIAC ABNORMALITIES", "keratosis palmoplantaris arrythmogenic cardiomyopathy woolly hair", "Keratosis palmoplantaris and arrhythmogenic cardiomyopathy syndrome", "Keratosis palmoplantaris and arrhythmogenic cardiomyopathy syndrome (disorder)", "cardiomyopathy, arrhythmogenic right ventricular, with skin, hair, and nail abnormalities", "CARDIOMYOPATHY, ARRHYTHMOGENIC RIGHT VENTRICULAR, WITH SKIN, HAIR, AND NAIL ABNORMALITIES", "Palmoplantar keratoderma with arrhythmogenic right ventricular cardiomyopathy and woolly hair", "palmoplantar keratoderma with arrhythmogenic right ventricular cardiomyopathy and woolly hair", "PALMOPLANTAR KERATODERMA WITH ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY AND WOOLLY HAIR"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Naxos disease", "shortest_name_length": 3}
{"curie": "UMLS:C1334240", "names": ["Intracranial Germinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intracranial Germinoma", "shortest_name_length": 22}
{"curie": "MONDO:0000627", "names": ["benign endocrine tumor", "Benign endocrine tumor", "Benign Endocrine Tumor", "Benign endocrine tumour", "Benign Endocrine Neoplasm", "benign endocrine neoplasm", "Benign endocrine neoplasm", "Endocrine neoplasms benign", "Benign Endocrine Gland Tumor", "benign endocrine gland tumor", "Benign endocrine neoplasm NOS", "Benign Tumor of Endocrine Gland", "endocrine gland benign neoplasm", "benign tumor of endocrine gland", "Benign tumor of endocrine gland", "endocrine organ benign neoplasm", "benign endocrine gland neoplasm", "Benign Endocrine Gland Neoplasm", "benign tumor of endocrine glands", "Benign tumour of endocrine gland", "benign neoplasm of endocrine gland", "Benign neoplasm of endocrine gland", "Benign Neoplasm of Endocrine Gland", "benign tumor of the endocrine gland", "Benign Tumor of the Endocrine Gland", "benign neoplasm of endocrine glands", "Benign Neoplasm of the Endocrine Gland", "benign neoplasm of the endocrine gland", "Benign neoplasm of endocrine gland, NOS", "Benign neoplasm of endocrine gland (disorder)", "Benign neoplasm of unspecified endocrine gland", "Benign neoplasm of endocrine gland, unspecified", "benign neoplasm of endocrine glands (diagnosis)", "Benign endocrine tumor (morphologic abnormality)", "Benign neoplasm of endocrine gland, site unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign endocrine neoplasm", "shortest_name_length": 22}
{"curie": "UMLS:C2609105", "names": ["Respiratory tract inflammation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Respiratory tract inflammation", "shortest_name_length": 30}
{"curie": "UMLS:C1304299", "names": ["Pilar Basal Cell Carcinoma", "Keratotic basal cell carcinoma", "Keratotic Basal Cell Carcinoma", "Basal cell carcinoma - keratotic", "Skin Keratotic Basal Cell Carcinoma", "Basal cell carcinoma - keratotic (disorder)", "Basal cell carcinoma - keratotic (diagnosis)", "malignant neoplasm carcinoma basal cell keratotic", "Keratotic basal cell carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Basal cell carcinoma - keratotic", "shortest_name_length": 26}
{"curie": "UMLS:C0854776", "names": ["Unresectable Pancreatic Cancer", "Unresectable Pancreatic Carcinoma", "Non-Resectable Pancreas Carcinoma", "Pancreatic carcinoma non-resectable", "Non-Resectable Pancreatic Carcinoma", "Non-Resectable Carcinoma of Pancreas", "Pancreatic Carcinoma, Non-Resectable", "Non-Resectable Carcinoma of the Pancreas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic carcinoma non-resectable", "shortest_name_length": 30}
{"curie": "MONDO:0007429", "names": ["DOA+", "optic atrophy plus syndrome", "optic atrophy 1 and deafness", "DOMINANT OPTIC ATROPHY PLUS SYNDROME", "dominant optic atrophy plus syndrome", "ADOA (autosomal dominant optic atrophy) plus", "Autosomal dominant optic atrophy plus syndrome", "optic atrophy hereditary dominant plus syndrome", "Optic atrophy-deafness-polyneuropathy-myopathy syndrome", "Autosomal dominant optic atrophy plus syndrome (disorder)", "Autosomal dominant optic atrophy plus syndrome (diagnosis)", "Optic atrophy-hearing loss-polyneuropathy-myopathy syndrome", "OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY", "optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy", "shortest_name_length": 4}
{"curie": "MONDO:0023061", "names": ["enamel hypoplasia cataract hydrocephaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "enamel hypoplasia cataract hydrocephaly", "shortest_name_length": 39}
{"curie": "MONDO:0019344", "names": ["AS syndrome", "Anti-Jo1 syndrome", "anti-Jo1 syndrome", "Antisynthetase syndrome", "antisynthetase syndrome", "Antisynthetase syndrome (disorder)", "antisynthetase syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "antisynthetase syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0017621", "names": ["CSID with starch and lactose intolerance", "disaccharide intolerance with starch and lactose intolerance", "congenital sucrose intolerance with starch and lactose intolerance", "congenital sucrase-isomaltase deficiency with starch and lactose intolerance", "congenital sucrase-isomaltose malabsorption with starch and lactose intolerance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital sucrase-isomaltase deficiency with starch and lactose intolerance", "shortest_name_length": 40}
{"curie": "MONDO:0008061", "names": ["NPS", "NPS1", "NPS 1", "Fong Disease", "FONG DISEASE", "Fong disease", "Disease, Fong", "FONG SYNDROME", "fong syndrome", "iliac horn syndrome", "Osterreicher-Turner", "onychoosteodysplasia", "Pelvic Horn Syndrome", "Onychoosteodysplasia", "ONYCHOOSTEODYSPLASIA", "Nail patella syndrome", "Nail Patella Syndrome", "NAIL-PATELLA SYNDROME", "osteo-onychodysplasia", "Nail-Patella Syndrome", "Nail-patella syndrome", "Syndrome, Pelvic Horn", "Turner-Kiser syndrome", "Osterreicher Syndrome", "nail-patella syndrome", "nail patella syndrome", "Syndrome, Nail-Patella", "TURNER-KIESER SYNDROME", "Turner-Kieser syndrome", "arthro-onychodysplasia", "Turner Kieser syndrome", "Syndrome, Osterreicher", "nail patella; syndrome", "turner kieser syndrome", "Turner-Kieser Syndrome", "syndrome; nail patella", "turner-kieser syndrome", "Turner Kieser Syndrome", "Syndrome, Turner-Kieser", "hereditary onychoostedysplasia", "Hereditary onycho-osteodysplasia", "hereditary Osteo-onychodysplasia", "Nail-patella syndrome (disorder)", "Hereditary Onycho-Osteodysplasia", "Hereditary Osteo-Onychodysplasia", "Hereditary osteo-onychodysplasia", "Osteo-Onychodysplasia, Hereditary", "Osteo Onychodysplasia, Hereditary", "Hereditary Osteo-Onychodysplasias", "nail-patella syndrome (diagnosis)", "Osteo-Onychodysplasias, Hereditary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nail-patella syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C0851881", "names": ["enterococcal infection", "Enterococcal infection", "enterococcal infections", "Enterococcal infections", "Enterococcal infection NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Enterococcal infection", "shortest_name_length": 22}
{"curie": "UMLS:C0752305", "names": ["Anoxic-ischemic encephalopathy", "Anoxic Ischemic Encephalopathy", "Anoxic-Ischemic Encephalopathy", "anoxic-ischemic encephalopathy", "Anoxic-ischaemic encephalopathy", "Encephalopathy, Anoxic-Ischemic", "Encephalopathy, Anoxic Ischemic", "Anoxic-Ischemic Encephalopathies", "Encephalopathies, Anoxic-Ischemic", "Anoxic-ischemic encephalopathy (disorder)", "anoxic-ischemic encephalopathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anoxic-Ischemic Encephalopathy", "shortest_name_length": 30}
{"curie": "MONDO:0019380", "names": ["WEE", "Encephalitis western equine", "Western equine encephalitis", "Western Equine Encephalitis", "western equine encephalitis", "western equine; encephalitis", "Encephalitis, Western Equine", "western; equine encephalitis", "encephalitis; western equine", "Encephalitis, Western equine", "ENCEPHALITIS, WESTERN EQUINE", "Equine Encephalitis, Western", "WESTERN EQUINE ENCEPHALOMYELITIS", "Western Equine Encephalomyelitis", "western equine encephalomyelitis", "Western equine encephalomyelitis", "Encephalomyelitis, Western Equine", "Western Equine Encephalitis (WEE)", "WEE - Western equine encephalitis", "Equine encephalitis, Western (WEE)", "Western equine encephalitis (disorder)", "Western equine encephalitis (diagnosis)", "Western equine encephalitis virus infection", "Western equine encephalitis virus infectious encephalitis", "Western equine encephalitis virus caused infectious encephalitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "western equine encephalitis", "shortest_name_length": 3}
{"curie": "MONDO:0010817", "names": ["DFNA2A", "autosomal dominant deafness 2A", "deafness, autosomal dominant 2A", "deafness, autosomal dominant 2a", "Deafness, Autosomal Dominant 2A", "DEAFNESS, AUTOSOMAL DOMINANT 2A", "deafness, autosomal dominant type 2A", "autosomal dominant nonsyndromic deafness 2A", "KCNQ4 autosomal dominant nonsyndromic deafness", "autosomal dominant nonsyndromic hearing loss 2A", "autosomal dominant nonsyndromic deafness type 2A", "autosomal dominant nonsyndromic deafness caused by mutation in KCNQ4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 2A", "shortest_name_length": 6}
{"curie": "MONDO:0000396", "names": ["Little's disease", "cerebrospasticity", "Spastic cerebral palsy", "cerebral palsy spastic", "spastic cerebral palsy", "Spastic Cerebral Palsy", "Cerebral Palsy, Spastic", "Cerebral palsy, spastic", "Spastic Cerebral Palsies", "Pyramidal cerebral palsy", "hypertonic cerebral palsy", "Spastic cerebral palsy NOS", "Spastic infantile paralysis", "cerebral; paralysis, spastic", "Congenital spastic paralysis", "paralysis; cerebral, spastic", "Infantile spastic cerebral palsy", "Congenital spastic cerebral palsy", "Spastic cerebral palsy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic cerebral palsy", "shortest_name_length": 16}
{"curie": "MONDO:0018061", "names": ["Pinheiro-Freire Maia-Miranda syndrome", "Pinheiro Freire-Maia Miranda syndrome", "Pinheiro, Freire Maia, Miranda syndrome", "Trichodermodysplasia with dental alterations", "trichodermodysplasia-dental alterations syndrome", "Trichodermodysplasia-dental alterations syndrome", "Trichodermodysplasia and dental alterations syndrome", "Trichodermodysplasia and dental alterations syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichodermodysplasia-dental alterations syndrome", "shortest_name_length": 37}
{"curie": "MONDO:0036484", "names": ["CMTDIG", "Charcot-Marie-Tooth disease dominant intermediate G", "CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G", "Charcot-Marie-Tooth disease, dominant intermediate G"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease, dominant intermediate G", "shortest_name_length": 6}
{"curie": "MONDO:0005407", "names": ["pediatric eosinophilic esophagitis", "childhood eosinophilic esophagitis", "eosinophilic esophagitis of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood eosinophilic esophagitis", "shortest_name_length": 34}
{"curie": "UMLS:C5206869", "names": ["Non-Invasive Cribriform Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Invasive Cribriform Carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0014691", "names": ["NS9", "Noonan syndrome 9", "Noonan Syndrome 9", "NOONAN SYNDROME 9", "SOS2 Noonan syndrome", "Noonan syndrome type 9", "Noonan syndrome caused by mutation in SOS2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Noonan syndrome 9", "shortest_name_length": 3}
{"curie": "UMLS:C0270720", "names": ["Hydrocephalus ex vacuo", "hydrocephalus ex vacuo", "Hydrocephalus Ex Vacuo", "hydrocephalus ex-vacuo", "Hydrocephalus Ex-Vacuo", "Hydrocephalus, ex vacuo", "Hydrocephalus Ex-Vacuos", "Hydrocephalus ex vacuo (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hydrocephalus Ex-Vacuo", "shortest_name_length": 22}
{"curie": "MONDO:0011772", "names": ["CDG2D", "CDGIId", "CDG 2D", "CDG IId", "CDG-IId", "B4GALT1-CDG", "B4GALT1-CDG (CDG-IId)", "CDG syndrome type IId", "Beta-1,4-galactosyltransferase deficiency", "Congenital disorder of glycosylation type 2D", "B4GALT1-congenital disorder of glycosylation", "congenital disorder of glycosylation type 2d", "Congenital disorder of glycosylation type 2d", "congenital disorder of glycosylation type IId", "Congenital disorder of glycosylation type IId", "congenital disorder of glycosylation, type IId", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IId", "Carbohydrate deficient glycoprotein syndrome type 2d", "Carbohydrate deficient glycoprotein syndrome type IId", "carbohydrate deficient glycoprotein syndrome type IId", "Carbohydrate deficient glycoprotein syndrome type 2d (disorder)", "B4GALT1-CDG - Beta-1,4-galactosyltransferase deficiency congenital disorder of glycosylation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B4GALT1-congenital disorder of glycosylation", "shortest_name_length": 5}
{"curie": "MONDO:0011697", "names": ["WS2C", "Waardenburg syndrome type 2C", "WAARDENBURG SYNDROME, TYPE 2C", "Waardenburg Syndrome, Type 2C", "Waardenburg syndrome, type 2C", "Waardenburg syndrome type IIC", "WAARDENBURG SYNDROME, TYPE IIC", "Waardenburg Syndrome, Type IIC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Waardenburg syndrome type 2C", "shortest_name_length": 4}
{"curie": "UMLS:C5420667", "names": ["Refractory Intrahepatic Cholangiocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Intrahepatic Cholangiocarcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0006522", "names": ["acquired keratosis", "Acquired Keratoderma", "acquired keratoderma", "Acquired keratoderma", "keratoderma acquired", "keratoderma, acquired", "Keratoderma, acquired", "Keratoderma - acquired", "keratoderma - acquired", "keratodermia; acquired", "acquired; keratodermia", "Keratoderma acquisitum", "acquired hyperkeratosis", "Acquired keratoderma, NOS", "Acquired hyperkeratosis NOS", "Acquired keratoderma (disorder)", "acquired keratoderma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired keratosis", "shortest_name_length": 18}
{"curie": "MONDO:0017572", "names": ["TBE", "Far Eastern TBE", "Taiga encephalitis", "taiga encephalitis", "Diphasic milk fever", "taiga; encephalitis", "encephalitis; taiga", "Biundulant milk fever", "Tick Borne Encephalitis", "tick-borne encephalitis", "Tick-Borne Encephalitis", "tick borne encephalitis", "Tick-borne encephalitis", "Encephalitis, Tick-borne", "Encephalitis, Tick Borne", "Encephalitis, Tick-Borne", "Forest-spring encephalitis", "west-Siberian encephalitis", "Diphasic meningoencephalitis", "Czechoslovakian; encephalitis", "Tick-borne viral encephalitis", "Central european encephalitis", "central European encephalitis", "Central European Encephalitis", "Central European encephalitis", "Tick-Borne Viral Encephalitis", "encephalitis; Czechoslovakian", "encephalitis; Central European", "Central European; encephalitis", "Encephalitis, Central European", "Biundulant meningoencephalitis", "Far Eastern Russian Encephalitis", "Siberian tick-borne encephalitis", "Encephalitis, Far Eastern Russian", "Russian Spring-Summer Encephalitis", "Russian spring-summer encephalitis", "Russian Spring-Summer encephalitis", "Russian Spring Summer Encephalitis", "Tick-borne viral encephalitis, NOS", "Encephalitis, Russian Spring-Summer", "Far Eastern tick-borne encephalitis", "Central European viral encephalitis", "CEE - Central European encephalitis", "Spring-Summer Encephalitis, Russian", "Russian; spring-summer encephalitis", "Encephalitis, Russian Spring Summer", "encephalitis; Russian, spring-summer", "encephalitis due to tick-borne virus", "Viral encephalitis transmitted by tick", "East Russian spring-summer encephalitis", "Central European encephalitis (disorder)", "Central European tick-borne encephalitis", "Western European tick-borne encephalitis", "RSSE - Russian spring-summer encephalitis", "Russian spring-summer [taiga] encephalitis", "summer; Russian spring-summer encephalitis", "Tick-borne viral encephalitis, unspecified", "Russian spring-summer encephalitis (disorder)", "TBE - Central European tick-borne encephalitis", "encephalitis due to tick-borne virus (diagnosis)", "Encephalitis due to tick-borne encephalitis virus", "encephalitis due to European tick-borne encephalitis virus", "encephalitis due to Far Eastern tick-borne encephalitis virus", "Viral encephalitis transmitted by tick (navigational concept)", "Encephalitis due to Far Eastern tick-borne encephalitis virus", "infection; viral, central nervous system, encephalitis, tick-borne", "Encephalitis due to European subtype of tick-borne encephalitis virus", "encephalitis due to European tick-borne encephalitis virus (diagnosis)", "Encephalitis due to tick-borne encephalitis virus (navigational concept)", "Far Eastern tick-borne encephalitis [Russian spring-summer encephalitis]", "encephalitis due to Far Eastern tick-borne encephalitis virus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tick-borne encephalitis", "shortest_name_length": 3}
{"curie": "UMLS:C0750900", "names": ["Focal Onset Alzheimer's Disease", "Alzheimer's Disease, Focal Onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alzheimer's Disease, Focal Onset", "shortest_name_length": 31}
{"curie": "UMLS:C5555930", "names": ["Cerebellar Peduncle Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebellar Peduncle Neoplasm", "shortest_name_length": 28}
{"curie": "MONDO:0018786", "names": ["PADMAL", "pontine autosomal dominant microangiopathy with leukoencephalopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pontine autosomal dominant microangiopathy with leukoencephalopathy", "shortest_name_length": 6}
{"curie": "UMLS:C1142140", "names": ["Pseudomonal bacteremia", "Pseudomonal bacteraemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pseudomonal bacteremia", "shortest_name_length": 22}
{"curie": "MONDO:0005413", "names": ["cystic fibrosis associated meconium ileus", "cystic fibrosis associated meconium ileum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cystic fibrosis associated meconium ileus", "shortest_name_length": 41}
{"curie": "MONDO:0022733", "names": ["choreoacanthocytosis amyotrophic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choreoacanthocytosis amyotrophic", "shortest_name_length": 32}
{"curie": "UMLS:C0264315", "names": ["glottis edema", "edema glottic", "GLOTTIC EDEMA", "EDEMA GLOTTIS", "Edema glottis", "glottic edema", "Glottic edema", "Glottic oedema", "Oedema glottis", "glottis; edema", "GLOTTIC OEDEMA", "edema; glottis", "glottic oedema", "Edema, glottis", "Edema of glottis", "edema of glottis", "Oedema of glottis", "Edema (of) glottis", "Edema of glottis (disorder)", "edema of glottis (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Edema of glottis", "shortest_name_length": 13}
{"curie": "MONDO:0007814", "names": ["immune deficiency, familial variable", "Immune Deficiency, Familial Variable", "IMMUNE DEFICIENCY, FAMILIAL VARIABLE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immune deficiency, familial variable", "shortest_name_length": 36}
{"curie": "MONDO:0012161", "names": ["familial CD8 deficiency", "Familial CD8 deficiency", "CD8 Deficiency, Familial", "CD8 deficiency, familial", "CD8 DEFICIENCY, FAMILIAL", "Susceptibility to respiratory infection associated with CD8alpha chain mutation", "Susceptibility to respiratory infections associated with CD8alpha chain mutation", "susceptibility to respiratory infections associated with CD8alpha chain mutation", "Susceptibility to respiratory infection associated with CD8alpha chain mutation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "susceptibility to respiratory infections associated with CD8alpha chain mutation", "shortest_name_length": 23}
{"curie": "MONDO:0011681", "names": ["EA4", "PATX", "Episodic ataxia type 4", "episodic ataxia type 4", "EPISODIC ATAXIA, TYPE 4", "Episodic Ataxia, Type 4", "episodic ataxia, type 4", "Episodic ataxia type 4 (disorder)", "Periodic Vestibulocerebellar Ataxia", "Periodic vestibulocerebellar ataxia", "periodic vestibulocerebellar ataxia", "PERIODIC VESTIBULOCEREBELLAR ATAXIA", "Ataxia, Periodic Vestibulocerebellar", "ataxia, periodic vestibulocerebellar", "ATAXIA, PERIODIC VESTIBULOCEREBELLAR"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "episodic ataxia type 4", "shortest_name_length": 3}
{"curie": "UMLS:C1142160", "names": ["Application site discoloration", "Application site discolouration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Application site discoloration", "shortest_name_length": 30}
{"curie": "MONDO:0002695", "names": ["Sagittal Sinus Thromboses", "SAGITTAL SINUS THROMBOSIS", "Sagittal Sinus Thrombosis", "sagittal sinus thrombosis", "Sagittal sinus thrombosis", "Sinus Thromboses, Sagittal", "Thrombosis, Sagittal Sinus", "Thromboses, Sagittal Sinus", "Sinus Thrombosis, Sagittal", "Superior sagittal sinus thrombosis", "sagittal sinus superior thrombosis", "THROMBOSIS, SUPERIOR SAGITTAL SINUS", "Thrombosis of superior sagittal sinus", "thrombosis of superior sagittal sinus", "THROMBOSIS, SUPERIOR LONGITUDINAL SINUS", "thrombosis of superior longitudinal sinus", "Thrombosis of superior longitudinal sinus", "Cerebral venous thrombosis of sagittal sinus", "Thrombosis of superior sagittal sinus (disorder)", "cerebral vein thrombosis of superior sagittal sinus", "Thrombosis of superior longitudinal sinus (disorder)", "cerebral vein thrombosis of superior sagittal sinus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sagittal sinus thrombosis", "shortest_name_length": 25}
{"curie": "MONDO:0023258", "names": ["G6P translocase deficiency", "SLC37A4 glycogen storage disease I", "glucose-6-phosphate translocase deficiency", "Glucose-6-phosphate translocase deficiency", "glycogen storage disease type 1 due to SLC37A4 mutation", "glycogen storage disease I caused by mutation in SLC37A4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease type 1 due to SLC37A4 mutation", "shortest_name_length": 26}
{"curie": "UMLS:C4527067", "names": ["Pathologic Stage I Merkel Cell Carcinoma AJCC v8", "Pathologic Stage I Neuroendocrine Carcinoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage I Merkel Cell Carcinoma AJCC v8", "shortest_name_length": 48}
{"curie": "UMLS:C0747733", "names": ["polychondritis", "Polychondritis", "POLYCHONDRITIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Polychondritis", "shortest_name_length": 14}
{"curie": "MONDO:0010494", "names": ["LSDMCA3", "LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 3", "linear skin defects with multiple congenital anomalies 3", "NDUFB11 microphthalmia with linear skin defects syndrome", "linear skin defects with multiple congenital anomalies type 3", "linear skin defects with cardiomyopathy and Other congenital anomalies", "LINEAR SKIN DEFECTS WITH CARDIOMYOPATHY AND OTHER CONGENITAL ANOMALIES", "linear skin defects with cardiomyopathy and other congenital anomalies", "linear skin defects with multiple congenital anomalies 3, X-linked dominant", "microphthalmia with linear skin defects syndrome caused by mutation in NDUFB11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "linear skin defects with multiple congenital anomalies 3", "shortest_name_length": 7}
{"curie": "UMLS:C3899989", "names": ["Autosomal Dominant Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Autosomal Dominant Disorder", "shortest_name_length": 27}
{"curie": "UMLS:C1567427", "names": ["Bilateral Multicystic Dysplastic Kidneys"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bilateral Multicystic Dysplastic Kidneys", "shortest_name_length": 40}
{"curie": "MONDO:0044889", "names": ["HGBL", "High-grade B-cell lymphoma", "High grade B-cell lymphoma", "High-Grade B-Cell Lymphoma", "high grade B-cell lymphoma", "High Grade B-Cell Lymphoma", "high-grade B-cell lymphoma", "High-grade B-cell lymphoma, NOS", "High grade B-cell lymphoma (disorder)", "High grade B-cell lymphoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "high grade B-cell lymphoma", "shortest_name_length": 4}
{"curie": "UMLS:C4688316", "names": ["Refractory Breast Cancer", "Refractory Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Breast Carcinoma", "shortest_name_length": 24}
{"curie": "MONDO:0006393", "names": ["rectal TSA", "Rectal TSA", "rectal serrated adenoma", "Rectal Serrated Adenoma", "rectal serrated adenoma type II", "Rectal Serrated Adenoma Type II", "Rectal Traditional Serrated Adenoma", "rectal traditional serrated adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rectal traditional serrated adenoma", "shortest_name_length": 10}
{"curie": "MONDO:0021121", "names": ["Angioendothelioma", "angioendothelioma", "hemangioendothelioma", "Hemangioendothelioma", "Hemangio Endothelioma", "Hemangioendotheliomas", "Vascular Endothelioma", "Haemangioendothelioma", "haemangioendothelioma", "vascular endothelioma", "hemangioendotheliomas", "Hemangio-Endothelioma", "Hemangio-Endotheliomas", "Endothelioma, Vascular", "Vascular Endotheliomas", "Endotheliomas, Vascular", "[M]Hemangioendothelioma", "[M]Haemangioendothelioma", "Hemangioendothelioma NOS", "Hemangioendothelioma, NOS", "Haemangioendothelioma NOS", "Haemangioendothelioma, NOS", "Hemangioendothelioma (disorder)", "hemangioendothelioma (diagnosis)", "Hemangioendothelioma (morphologic abnormality)", "neoplasm - soft tissue types blood vessel hemangioendothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemangioendothelioma", "shortest_name_length": 17}
{"curie": "MONDO:0018804", "names": ["MYO5B deficiency", "MYO5B-related progressive familial intrahepatic cholestasis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MYO5B-related progressive familial intrahepatic cholestasis", "shortest_name_length": 16}
{"curie": "MONDO:0022895", "names": ["craniosynostosis cleft lip palate arthrogryposis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniosynostosis cleft lip palate arthrogryposis", "shortest_name_length": 48}
{"curie": "MONDO:0011283", "names": ["MTDPS1", "Polip syndrome", "POLIP Syndrome", "POLIP SYNDROME", "MNGIE, TYMP-RELATED", "Mngie, tymp-related", "Dacarbazine/Oblimersen", "Mitochondrial DNA Depletion Syndrome 1", "mitochondrial DNA depletion syndrome 1", "mitochondrial DNA depletion syndrome type 1", "myoneurogastrointestinal encephalopathy syndrome", "MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE)", "mitochondrial DNA depletion syndrome 1 (MNGIE type)", "mitochondrial neurogastrointestinal encephalopathy syndrome, TYMP-related", "mitochondrial neurogastrointestinal encephalopathy syndrome, tymp-related", "POLYNEUROPATHY, OPHTHALMOPLEGIA, LEUKOENCEPHALOPATHY, AND INTESTINAL PSEUDOOBSTRUCTION", "polyneuropathy, ophthalmoplegia, leukoencephalopathy, and intestinal pseudoobstruction", "Polyneuropathy, ophthalmoplegia, leukoencephalopathy, and intestinal pseudoobstruction", "Polyneuropathy, Ophthalmoplegia, Leukoencephalopathy, and Intestinal Pseudo-Obstruction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial DNA depletion syndrome 1", "shortest_name_length": 6}
{"curie": "UMLS:C4521741", "names": ["IB", "Stage IB Esophageal Squamous Cell Cancer", "Pathologic Stage IB Esophageal Squamous Cell Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IB Esophageal Squamous Cell Carcinoma AJCC v8", "shortest_name_length": 2}
{"curie": "UMLS:C0032320", "names": ["Pneumoabdomen", "Pneumoperitoneum", "PNEUMOPERITONEUM", "pneumoperitoneum", "Free air in abdomen", "PERITONEAL FREE AIR", "PP - Pneumoperitoneum", "Intraperitoneal free air", "Peritoneal cavity free air", "Pneumoperitoneum (disorder)", "Free air in peritoneal cavity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pneumoperitoneum", "shortest_name_length": 13}
{"curie": "UMLS:C3273122", "names": ["Gallbladder MANEC", "Gallbladder Mixed Adenoneuroendocrine Cancer", "Gallbladder Mixed Adenoneuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gallbladder Mixed Adenoneuroendocrine Carcinoma", "shortest_name_length": 17}
{"curie": "MONDO:0100032", "names": ["familial temporal lobe epilepsy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial temporal lobe epilepsy syndrome", "shortest_name_length": 40}
{"curie": "MONDO:0042982", "names": ["GATA2 deficiency", "MonoMAC Syndrome", "GATA2 Deficiency", "Immunodeficiency 21", "GATA2 deficiency/MonoMac syndrome", "GATA2 deficiency with susceptibility to MDS/AML", "Monocytopenia and Mycobacterial Infection Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "GATA2 deficiency with susceptibility to MDS/AML", "shortest_name_length": 16}
{"curie": "MONDO:0004094", "names": ["multiple skull base meningioma", "multiple skull base meningiomas", "Multiple Skull Base Meningiomas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple skull base meningioma", "shortest_name_length": 30}
{"curie": "MONDO:0017435", "names": ["PPS", "Popliteal web syndrome", "popliteal web syndrome", "syndrome; popliteal web", "popliteal syndrome; web", "web; popliteal syndrome", "popliteal web; syndrome", "Popliteal Pterygium Syndrome", "Popliteal pterygium syndrome", "popliteal pterygium syndrome", "POPLITEAL PTERYGIUM SYNDROME", "FACIOGENITOPOPLITEAL SYNDROME", "Faciogenitopopliteal Syndrome", "facio-genito-popliteal syndrome", "Facio-genito-popliteal syndrome", "Facio-Genito-Popliteal Syndrome", "Popliteal pterygium syndrome (disorder)", "popliteal pterygium syndrome (diagnosis)", "Autosomal dominant popliteal pterygium syndrome", "Autosomal Dominant Popliteal Pterygium Syndrome", "Autosomal dominant popliteal pterygium syndrome (disorder)", "Cleft Lip-Palate, Paramedian Mucous Cysts Of The Lower Lip, Popliteal Pterygium, Digital And Genital Anomalies", "CLEFT LIP/PALATE, PARAMEDIAN MUCOUS CYSTS OF THE LOWER LIP, POPLITEAL PTERYGIUM, DIGITAL AND GENITAL ANOMALIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "popliteal pterygium syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0010677", "names": ["Muscular Dystrophy, Mabry Type", "MUSCULAR DYSTROPHY, MABRY TYPE", "muscular dystrophy, Mabry type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy, Mabry type", "shortest_name_length": 30}
{"curie": "MONDO:0018371", "names": ["distal nebulin myopathy", "nebulin-related early-onset distal myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nebulin-related early-onset distal myopathy", "shortest_name_length": 23}
{"curie": "MONDO:0003136", "names": ["anti-GBM antibody disease", "Anti-GBM Antibody Disease", "anti-GBM glomerulonephritis", "anti-basement membrane glomerulonephritis", "Anti-Basement Membrane Glomerulonephritis", "Anti-Glomerular Basement Membrane Antibody Disease", "anti-glomerular basement Membrane antibody disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anti-basement membrane glomerulonephritis", "shortest_name_length": 25}
{"curie": "UMLS:C0542007", "names": ["Hematoma cerebral", "cerebral hematoma", "Cerebral hematoma", "CEREBRAL HEMATOMA", "HEMATOMA CEREBRAL", "Cerebral haematoma", "cerebral haematoma", "Haematoma cerebral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebral hematoma", "shortest_name_length": 17}
{"curie": "MONDO:0016885", "names": ["partial monosomy of chromosome 3p", "partial deletion of chromosome 3p", "partial deletion of the short arm of chromosome 3", "partial monosomy of the short arm of chromosome 3", "partial deletion of the short arm of chromosome type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of the short arm of chromosome 3", "shortest_name_length": 33}
{"curie": "MONDO:0011003", "names": ["CDCD2", "CMD1E", "dilated cardiomyopathy 1E", "Cardiomyopathy, Dilated, 1E", "CARDIOMYOPATHY, DILATED, 1E", "cardiomyopathy, dilated, 1E", "dilated cardiomyopathy type 1E", "cardiomyopathy, dilated, type 1E", "SCN5A familial isolated dilated cardiomyopathy", "dilated cardiomyopathy with conduction defect 2", "cardiomyopathy, dilated, with conduction defect 2", "CARDIOMYOPATHY, DILATED, WITH CONDUCTION DEFECT 2", "Cardiomyopathy, Dilated, with Conduction Defect 2", "cardiomyopathy dilated with conduction defect type 2", "dilated cardiomyopathy with conduction disorder and arrhythmia", "cardiomyopathy, dilated, with conduction disorder and arrhythmia", "CARDIOMYOPATHY, DILATED, WITH CONDUCTION DISORDER AND ARRHYTHMIA", "Cardiomyopathy, Dilated, with Conduction Disorder and Arrhythmia", "familial isolated dilated cardiomyopathy caused by mutation in SCN5A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1E", "shortest_name_length": 5}
{"curie": "UMLS:C1135746", "names": ["Serogroup B Meningococcal Meningitis", "Meningococcal Meningitis, Serogroup B", "Meningitis, Meningococcal, Serogroup B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meningitis, Meningococcal, Serogroup B", "shortest_name_length": 36}
{"curie": "MONDO:0020744", "names": ["mobitz i", "Möbitz I", "Mobitz I", "Wenckebach", "wenckebach", "WENCKEBACH", "Mobitz type I", "Block;Wenckebach", "Wenckebach Block", "Wenckebach block", "WENCKEBACH PAUSE", "wenckebach block", "block; Wenckebach", "Wenckebach; block", "Wenckebach's block", "Wenckebach phenomenon", "WENCKEBACH PHENOMENON", "wenckebach phenomenon", "Wenckebach; phenomenon", "phenomenon; Wenckebach", "Wenckebach's phenomenon", "type 1 2nd degree AV block", "Type 1 2nd degree AV Block", "AV block-2nd degree-type 1", "Type 1 Second Degree AV Block", "type 1 second degree AV block", "Mobitz I atrioventricular block", "AV BLOCK SECOND DEGREE MOBITZ I", "Wenckebach's incomplete AV block", "AV block second degree Möbitz type I", "AV Block Second Degree Möbitz Type I", "Mobitz type 1 atrioventricular block", "AV block second degree Mobitz type I", "Mobitz Type I Second Degree AV Block", "Mobitz type I second degree AV block", "Möbitz type I second degree AV block", "Mobitz type I atrioventricular block", "AV Block Second Degree Mobitz Type I", "Möbitz Type I Second Degree AV Block", "Second degree AV block, Mobitz type I", "second degree A-V block, Mobitz type I", "A-V block second degree: Mobitz type I", "Incomplete atrioventricular block, Mobitz I", "Type 1 Second Degree Atrioventricular Block", "type 1 second degree atrioventricular block", "Second degree AV heart block - Mobitz type 1", "Mobitz type I Wenckebach atrioventricular block", "Incomplete atrioventricular block, Wenckebach's", "Mobitz type I incomplete atrioventricular block", "Mobitz type I atrioventricular block (diagnosis)", "Incomplete atrioventricular block, Mobitz type I", "Second Degree Atrioventricular Block Mobitz Type I", "second degree atrioventricular block Mobitz type I", "Mobitz type 1 second degree atrioventricular block", "second degree atrioventricular block Möbitz type I", "Second Degree Atrioventricular Block Möbitz Type I", "Mobitz type I incomplete atrioventricular block (disorder)", "Incomplete atrioventricular block, second degree, Mobitz I", "Incomplete atrioventricular block, second degree, Mobitz type I", "Incomplete atrioventricular block, with 2:1 atrioventricular block", "Incomplete atrioventricular block, with 2:1 atrioventricular response"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mobitz type I atrioventricular block", "shortest_name_length": 8}
{"curie": "MONDO:0005151", "names": ["dysendocrinism", "endocrinopathy", "Endocrinopathy", "endocrinopathies", "endocrine disease", "Endocrine disease", "Endocrine Disease", "disease endocrine", "ENDOCRINE PROBLEM", "endocrine problem", "DISORDER ENDOCRINE", "Disorder endocrine", "endocrine diseases", "Endocrine disorder", "IMBALANCE HORMONAL", "Disorder;endocrine", "diseases endocrine", "endocrine problems", "endocrine disorder", "Endocrine Diseases", "HORMONAL IMBALANCE", "Endocrine Disorder", "Disease, Endocrine", "disorder endocrine", "ENDOCRINE DISORDER", "ENDOCRINE DISORDERS", "Endocrine disorders", "disorder; endocrine", "endocrine; disorder", "Hormone disturbance", "endocrine disorders", "Endocrinopathy, NOS", "disorders endocrine", "Diseases, Endocrine", "Endocrine Disorders", "imbalance; endocrine", "endocrine; imbalance", "disturbance endocrine", "Endocrine disturbance", "disturbance; endocrine", "ENDOCRINE DISORDER NOS", "Endocrine disorder NOS", "ENDOCRINE PROBLEM, NOS", "Hormone disturbance NOS", "endocrine gland disease", "Endocrine disorder, NOS", "endocrine system disease", "Endocrine System Disease", "disorder endocrine gland", "General Endocrinopathies", "Endocrine system disease", "diseases endocrine gland", "ENDOCRINE DISORDER (NOS)", "disease endocrine system", "diseases endocrine glands", "Endocrine disturbance NOS", "Endocrine System Diseases", "diseases endocrine system", "endocrine system disorder", "Endocrine System Disorder", "Disease, Endocrine System", "System Disease, Endocrine", "endocrine system diseases", "Disease of endocrine gland", "disorders endocrine system", "System Diseases, Endocrine", "Diseases, Endocrine System", "Endocrine disturbance, NOS", "diseases endocrine systems", "disorders endocrine glands", "Endocrine glands--Diseases", "endocrine; gland, disorder", "Disorder of endocrine gland", "disease of endocrine system", "Disorder of Endocrine System", "disease (or disorder); gland", "Diseases of Endocrine System", "disorder of endocrine system", "Disorder of endocrine system", "Endocrine system disease, NOS", "Unspecified endocrine disorder", "Endocrine disorder, unspecified", "endocrine disorders (diagnosis)", "Disease of endocrine glands, NOS", "DISEASES OF THE ENDOCRINE SYSTEM", "of the endocrine diseases system", "diseases of the endocrine system", "Abnormality of the endocrine system", "endocrine system disease or disorder", "Thyroid or other glandular disorders", "thyroid or other glandular disorders", "Disorder of endocrine system (disorder)", "disease or disorder of endocrine system", "disease (or disorder); endocrine glands"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endocrine system disorder", "shortest_name_length": 14}
{"curie": "MONDO:0033361", "names": ["DEE52", "EIEE52", "early infantile epileptic encephalopathy 52", "developmental and epileptic encephalopathy 52", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 52", "epileptic encephalopathy, early infantile, 52", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 52", "developmental and epileptic encephalopathy, 52"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 52", "shortest_name_length": 5}
{"curie": "UMLS:C0751664", "names": ["Type I Canavan Disease", "Canavan Disease, Type I", "Neonatal Canavan Disease", "Canavan Disease, Neonatal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Canavan Disease, Neonatal", "shortest_name_length": 22}
{"curie": "MONDO:0021239", "names": ["tumor urethra", "urethra tumor", "Urethra Tumor", "urethra tumors", "Urethral tumor", "urethral tumor", "Urethral Tumor", "tumors urethra", "Urethra Tumors", "Urethral Tumors", "tumors urethral", "Tumors. Urethra", "tumors. urethra", "urethral tumors", "Urethral tumour", "tumor of urethra", "urethra neoplasm", "Urethra Neoplasm", "Tumor of urethra", "Tumor of Urethra", "urethral neoplasm", "Urethral neoplasm", "Tumour of urethra", "Neoplasm, Urethra", "Urethral Neoplasm", "urethra neoplasms", "Urethra Neoplasms", "neoplasms. urethra", "Neoplasms. Urethra", "urethral neoplasms", "Urethral Neoplasms", "Neoplasms, Urethra", "Neoplasm, Urethral", "Urethral neoplasms", "neoplasm of urethra", "Neoplasm of urethra", "Neoplasm of Urethra", "Neoplasms, Urethral", "Tumor of the Urethra", "tumor of the urethra", "Urethral neoplasm NOS", "Neoplasm of the urethra", "neoplasm of the urethra", "Neoplasm of the Urethra", "Neoplasia of the urethra", "urethra neoplasm (disease)", "Neoplasm of urethra (disorder)", "neoplasm of urethra (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urethra neoplasm", "shortest_name_length": 13}
{"curie": "MONDO:0011896", "names": ["PARK11", "Parkinson Disease 11", "Parkinson disease 11", "GIGYF2 hereditary late onset Parkinson disease", "susceptibility to autosomal dominant Parkinson disease 11", "Parkinson disease 11, autosomal dominant, susceptibility to", "PARKINSON DISEASE 11, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO", "hereditary late onset Parkinson disease caused by mutation in GIGYF2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parkinson disease 11, autosomal dominant, susceptibility to", "shortest_name_length": 6}
{"curie": "MONDO:0016915", "names": ["partial monosomy of chromosome 17q", "partial deletion of chromosome 17q", "partial monosomy of the long arm of chromosome 17", "partial deletion of the long arm of chromosome 17", "partial deletion of the long arm of chromosome type 17"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of the long arm of chromosome 17", "shortest_name_length": 34}
{"curie": "MONDO:0004250", "names": ["extrahepatic bile duct papillary adenoma", "Extrahepatic Bile Duct Papillary Adenoma", "papillary adenoma of extrahepatic bile duct", "Papillary Adenoma of Extrahepatic Bile Duct", "Papillary adenoma of the extrahepatic bile duct", "Papillary Adenoma of the Extrahepatic Bile Duct", "papillary adenoma of the extrahepatic bile duct", "papillary adenoma of extrahepatic bile duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extrahepatic bile duct papillary adenoma", "shortest_name_length": 40}
{"curie": "MONDO:0019281", "names": ["isolated hair shaft abnormality", "isolated genetic hair shaft abnormality"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated genetic hair shaft abnormality", "shortest_name_length": 31}
{"curie": "UMLS:C5669727", "names": ["Extramedullary Disease in Multiple Myeloma Involving the Kidney", "Extramedullary Disease in Plasma Cell Myeloma Involving the Kidney"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extramedullary Disease in Plasma Cell Myeloma Involving the Kidney", "shortest_name_length": 63}
{"curie": "MONDO:0007400", "names": ["JWS", "Jackson-Weiss Syndrome", "jackson-weiss syndrome", "jackson weiss syndrome", "JACKSON-WEISS SYNDROME", "Jackson-Weiss syndrome", "Jackson-Weiss syndrome (JWS)", "Jackson-Weiss syndrome (disorder)", "Acrocephalosyndactyly Jackson Weiss type", "Enlarged great toes and craniofacial abnormalities", "craniosynostosis, midfacial hypoplasia, and foot abnormalities", "CRANIOSYNOSTOSIS, MIDFACIAL HYPOPLASIA, AND FOOT ABNORMALITIES", "Craniosynostosis, midfacial hypoplasia, and foot abnormalities", "craniosynostosis-midfacial hypoplasia-foot abnormalities syndrome", "Craniosynostosis-midfacial hypoplasia-foot abnormalities syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jackson-Weiss syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0030449", "names": ["DFNB118", "deafness, autosomal recessive 118, with cochlear aplasia", "DEAFNESS, AUTOSOMAL RECESSIVE 118, WITH COCHLEAR APLASIA", "hearing loss, autosomal recessive 118, with cochlear aplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal recessive 118, with cochlear aplasia", "shortest_name_length": 7}
{"curie": "MONDO:0018664", "names": ["Ectopic heart", "ectopic heart", "ECTOPIA CORDIS", "Ectopia Cordis", "Ectopia cordis", "ectopic cordis", "ectopia cordis", "Cordis, Ectopia", "cordis; ectopia", "ectopia; cordis", "Extrathoracic heart", "ectopia cordis (disease)", "Ectopia cordis (disorder)", "ectopic cordis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectopia cordis", "shortest_name_length": 13}
{"curie": "MONDO:0016745", "names": ["DLM", "leptomeningeal melanomatosis", "diffuse leptomeningeal melanocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diffuse leptomeningeal melanocytosis", "shortest_name_length": 3}
{"curie": "MONDO:0011255", "names": ["MEHM", "VERLOES-LESENFANTS SYNDROME", "Verloes-Lesenfants syndrome", "macroblepharon, ectropion, hypertelorism, and macrostomia", "MACROBLEPHARON, ECTROPION, HYPERTELORISM, AND MACROSTOMIA", "macroblepharon-ectropion-hypertelorism-macrostomia syndrome", "mandibulofacial dysostosis-macroblepharon-macrostomia syndrome", "mandibulofacial dysostosis with macroblepharon and macrostomia", "MANDIBULOFACIAL DYSOSTOSIS WITH MACROBLEPHARON AND MACROSTOMIA", "Mandibulofacial Dysostosis with Macroblepharon and Macrostomia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mandibulofacial dysostosis-macroblepharon-macrostomia syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0020820", "names": ["DA2B1", "distal arthrogryposis type 2B1", "ARTHROGRYPOSIS, DISTAL, TYPE 2B1", "arthrogryposis, distal, type 2B1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal arthrogryposis type 2B1", "shortest_name_length": 5}
{"curie": "UMLS:C4551865", "names": ["Stage IA", "Stage IA Cancer of Testis", "stage IA cancer of testis", "stage IA testicular cancer", "Stage IA Testicular Cancer", "Stage IA Cancer of the Testis", "stage IA cancer of the testis", "stage IA testicular cancer AJCC v6", "stage IA testicular cancer AJCC v7", "Stage IA Testicular Cancer AJCC v7", "Stage IA Testicular Cancer AJCC v6", "Stage IA Testicular Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Testicular Cancer AJCC v6 and v7", "shortest_name_length": 8}
{"curie": "MONDO:0017569", "names": ["De Barsy syndrome", "de Barsy syndrome", "de Barsey syndrome", "de Barsy syndrome (disorder)", "Progeroid syndrome of De Barsy", "progeroid syndrome of de Barsy", "Progeroid syndrome of de Barsey", "De Barsy Moens Diercks syndrome", "de Barsey-Moens-Dierckx syndrome", "progeroid syndrome, de Barsy type", "progeroid syndrome, De Barsy type", "Progeroid syndrome, De Barsy type", "cutis laxa growth deficiency syndrome", "autosomal recessive cutis laxa type III", "Corneal clouding cutis laxa mental retardation", "Cutis laxa-corneal clouding-oligophrenia syndrome", "Cutis laxa, corneal clouding and mental retardation", "Cutis laxa, corneal clouding AND mental retardation", "corneal clouding, cutis laxa and mental retardation", "Cutis Laxa, Corneal Clouding, And Mental Retardation", "corneal clouding, cutis laxa and intellectual disability", "cutis laxa autosomal recessive type III (de Barsy syndrome)", "Cutis laxa-corneal clouding-oligophrenia syndrome (disorder)", "Cutis laxa-corneal clouding-intellectual disability syndrome", "cutis laxa-corneal clouding-intellectual disability syndrome", "cutis laxa autosomal recessive type III (de Barsy syndrome) (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "de Barsy syndrome", "shortest_name_length": 17}
{"curie": "UMLS:C4525694", "names": ["Stage II Appendix Neuroendocrine Tumor", "Stage II Appendix Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Appendix Neuroendocrine Tumor AJCC v8", "shortest_name_length": 38}
{"curie": "MONDO:0027653", "names": ["abacavir toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "abacavir toxicity", "shortest_name_length": 17}
{"curie": "MONDO:0005814", "names": ["Bowel cancer", "bowel cancer", "Bowel Cancer", "bowel cancers", "Cancer of bowel", "intestine cancer", "INTESTINAL CANCER", "intestinal cancer", "intestines cancer", "Intestinal Cancer", "Intestines Cancer", "Intestinal cancer", "intestinal cancers", "Cancer, Intestines", "Cancer, Intestinal", "Intestines--Cancer", "Intestines Cancers", "Intestinal Cancers", "Cancer of intestine", "Cancer of Intestine", "cancer of intestine", "Cancers, Intestinal", "Cancers, Intestines", "cancer of intestines", "Cancer of Intestines", "CA - Cancer of bowel", "Intestinal Neoplasms", "Cancer of the Intestine", "cancer of the intestine", "CA - Cancer of intestine", "Cancer of the Intestines", "Malignant Intestine Tumor", "malignant intestine tumor", "malignant intestinal tumor", "Malignant Intestinal Tumor", "malignant intestinal tumors", "Malignant Intestinal Tumors", "Malignant Tumor of Intestine", "malignant tumor of intestine", "intestinal tumors, malignant", "Intestinal Tumors, Malignant", "Malignant Intestine Neoplasm", "Malignant tumor of intestine", "malignant intestine neoplasm", "Malignant tumour of intestine", "malignant intestinal neoplasm", "Malignant Intestinal Neoplasm", "Malignant intestinal neoplasms", "Malignant Intestinal Neoplasms", "malignant intestinal neoplasms", "intestinal neoplasms, malignant", "Intestinal Neoplasms, Malignant", "Malignant Neoplasm of Intestine", "Malignant neoplasm of intestine", "malignant neoplasm of intestine", "Malignant Tumor of the Intestine", "malignant tumor of the intestine", "malignant neoplasm of the intestine", "Malignant neoplasm of intestine NOS", "Malignant Neoplasm of the Intestine", "malignant neoplasm of intestinal tract", "Malignant tumor of intestine (disorder)", "Malignant neoplasm of intestinal tract, NOS", "malignant neoplasm of intestinal tract (diagnosis)", "Malignant neoplasm of intestinal tract, part unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intestinal cancer", "shortest_name_length": 12}
{"curie": "UMLS:C0748505", "names": ["Metastatic sarcoma", "SARCOMA METASTATIC", "Sarcoma metastatic", "Metastatic Sarcoma", "sarcoma metastatic", "Sarcoma, metastatic", "Metastatic sarcoma (disorder)", "Metastatic sarcoma (diagnosis)", "Sarcoma, metastatic (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic sarcoma", "shortest_name_length": 18}
{"curie": "UMLS:C0235398", "names": ["DIABETES MELLITUS AGGRAVATED", "Diabetes mellitus aggravated", "Diabetes mellitus exacerbated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diabetes mellitus aggravated", "shortest_name_length": 28}
{"curie": "MONDO:0008843", "names": ["Feigenbaum-Bergeron-Richardson syndrome", "Feigenbaum Bergeron Richardson syndrome", "Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome", "atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome", "Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome", "Atherosclerosis-hearing loss-diabetes-epilepsy-nephropathy syndrome", "atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome", "Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome (disorder)", "atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome (diagnosis)", "Atherosclerosis, Premature, with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease", "ATHEROSCLEROSIS, PREMATURE, WITH DEAFNESS, NEPHROPATHY, DIABETES MELLITUS, PHOTOMYOCLONUS, AND DEGENERATIVE NEUROLOGIC DISEASE", "atherosclerosis, premature, with deafness, nephropathy, diabetes mellitus, photomyoclonus, and degenerative neurologic disease", "premature atherosclerosis with photomyoclonic epilepsy, deafness, diabetes mellitus, nephropathy, and neurodegenerative disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome", "shortest_name_length": 39}
{"curie": "MONDO:0007404", "names": ["monosomy 5p", "5p Syndrome", "Deletion 5p", "5p syndrome", "deletion 5p", "Monosomy 5p", "5p- syndrome", "5p- Syndrome", "5p- Syndromes", "Syndrome, 5p-", "Cat-Cry syndrome", "Cat Cry syndrome", "del(5p) syndrome", "cat cry syndrome", "Lejeune syndrome", "cry cat syndrome", "monosomy type 5p", "Cat Cry Syndrome", "Cat-Cry Syndrome", "CAT CRY SYNDROME", "5p Minus Syndrome", "cats cry syndrome", "5p minus syndrome", "Cat Cry Syndromes", "cat-cry; syndrome", "Syndrome, Cat Cry", "syndrome; cat-cry", "Syndromes, Cat Cry", "5p Minus Syndromes", "Minus Syndrome, 5p", "cat's cry syndrome", "Lejeune's syndrome", "Syndrome, 5p Minus", "cat crying syndrome", "Crying Cat Syndrome", "crying cat syndrome", "Syndromes, 5p Minus", "partial monosomy 5p", "Minus Syndromes, 5p", "5p deletion syndrome", "chat du cri syndrome", "Cri-du-Chat Syndrome", "cri du chat syndrome", "Syndrome, Crying Cat", "Crying Cat Syndromes", "CRI-DU-CHAT SYNDROME", "Deletion 5p syndrome", "Cri-Du-Chat syndrome", "Cri du Chat Syndrome", "5p Deletion Syndrome", "Cri-du-chat syndrome", "cri-du-chat syndrome", "Cri du Chat syndrome", "chat cri du syndrome", "Cri du chat syndrome", "Cri Du Chat Syndrome", "Syndrome, 5p Deletion", "cris du chat syndrome", "Syndromes, Crying Cat", "Cri-du-Chat Syndromes", "cri du chats syndrome", "cri-du-chat syndromes", "Syndrome, Cri-du-Chat", "5p Deletion Syndromes", "Deletion Syndrome, 5p", "chromosome 5p monosomy", "Syndromes, Cri-du-Chat", "Deletion Syndromes, 5p", "Syndromes, 5p Deletion", "Chromosome 5p- Syndrome", "chromosome 5p- syndrome", "Syndrome, Chromosome 5p-", "5p- Syndrome, Chromosome", "Chromosome 5p- Syndromes", "Syndromes, Chromosome 5p-", "5p- Syndromes, Chromosome", "5P minus (partial) syndrome", "5p partial monosomy syndrome", "5p Partial Monosomy Syndrome", "Chromosome 5p Deletion Syndrome", "CHROMOSOME 5p DELETION SYNDROME", "chromosome 5p deletion syndrome", "Chromosome 5p deletion syndrome", "chromosome 5P deletion syndrome", "chromosome; 5 short arm deletion", "cri du chat syndrome (diagnosis)", "Partial monosomy of chromosome 5p", "Partial deletion of chromosome 5p", "deletion; short arm of chromosome 5", "Deletion of short arm of chromosome 5", "5p partial monosomy syndrome (disorder)", "Chromosome 5 Short Arm Deletion Syndrome", "chromosome 5 short arm deletion syndrome", "chromosome; syndrome, 5 short arm deletion", "syndrome; chromosome, 5 short arm deletion", "deletion of part of chromosome 5 short arm", "Deletion of Short Arm of Chromosome 5 Syndrome", "Partial monosomy of the short arm of chromosome 5", "Partial deletion of the short arm of chromosome 5", "Deletion of short arm of chromosome 5 (diagnosis)", "Partial deletion of short arm of chromosome 5 syndrome", "Chromosomal imbalance syndrome, pair 5, deletion, short arm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cri-du-chat syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0006483", "names": ["Urothelial Dysplasia", "Urothelial dysplasia", "urothelial dysplasia", "Urothelial cell dysplasia", "Transitional cell dysplasia", "Bladder Urothelial Dysplasia", "Low-grade intraurothelial neoplasia", "Bladder Low Grade Intraurothelial Neoplasia", "Low-Grade Bladder Intraurothelial Neoplasia", "Transitional Cell Dysplasia of the Urinary Tract", "transitional cell dysplasia of the urinary tract", "Transitional cell dysplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urothelial dysplasia", "shortest_name_length": 20}
{"curie": "MONDO:0007581", "names": ["EAR BUMP", "Ear Bump", "Ear bump", "EXCHONDROSIS OF PINNA, POSTERIOR", "exchondrosis of pinna, posterior", "Exchondrosis Of Pinna, Posterior"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exchondrosis of pinna, posterior", "shortest_name_length": 8}
{"curie": "UMLS:C2063866", "names": ["Refractory Depression", "Refractory Depressions", "Depression, Refractory", "Depressions, Refractory", "Therapy-Resistant Depression", "Therapy Resistant Depression", "Depression, Therapy-Resistant", "Therapy-Resistant Depressions", "depression resistant treatment", "Treatment resistant depression", "Treatment Resistant Depression", "treatment resistant depression", "Depressions, Therapy-Resistant", "Treatment Resistant Depressions", "treatment-refractory depression", "Resistant Depression, Treatment", "Depression, Treatment Resistant", "Resistant Depressions, Treatment", "Depressions, Treatment Resistant", "Treatment-Resistant Depressive Disorder", "Depressive Disorder, Treatment Resistant", "Disorder, Treatment-Resistant Depressive", "Treatment-Resistant Depressive Disorders", "Depressive Disorder, Treatment-Resistant", "Treatment resistant depression (disorder)", "Depressive Disorders, Treatment-Resistant", "Disorders, Treatment-Resistant Depressive", "treatment-refractory depression (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Depressive Disorder, Treatment-Resistant", "shortest_name_length": 21}
{"curie": "UMLS:C1336267", "names": ["Stage III Renal Pelvis and Ureter Cancer", "Stage III Renal Pelvis and Ureter Carcinoma", "Stage III Renal Pelvis and Ureter Cancer AJCC v7", "Stage III Renal Pelvis and Ureter Carcinoma AJCC v7", "stage III transitional cell cancer of the renal pelvis and ureter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Renal Pelvis and Ureter Cancer AJCC v7", "shortest_name_length": 40}
{"curie": "UMLS:C4526611", "names": ["Stage IIIB Thymoma", "Stage IIIB Thymoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Thymoma AJCC v8", "shortest_name_length": 18}
{"curie": "MONDO:0015019", "names": ["YAOS", "YAO SYNDROME", "Yao syndrome", "NOD2-associated autoinflammatory disease", "NOD2-associated autoinflammatory disease (diagnosis)", "inflammatory disorder chronic NOD2-associated autoinflammatory disease", "Nucleotide binding oligomerization domain containing 2-associated autoinflammatory disease", "NOD2 (nucleotide binding oligomerization domain containing 2) associated autoinflammatory disease", "Nucleotide binding oligomerization domain containing 2-associated autoinflammatory disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Yao syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0005679", "names": ["bovine hemorrhagic syndrome", "Bovine Hemorrhagic Syndrome", "Hemorrhagic Syndrome, Bovine", "hemorrhagic syndrome, bovine", "Bovine Virus Diarrhea-Mucosal Disease", "bovine virus diarrhea-mucosal disease", "Bovine Virus Diarrhea Mucosal Disease", "Mucosal Disease, Bovine Viral Diarrhea"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bovine virus diarrhea-mucosal disease", "shortest_name_length": 27}
{"curie": "UMLS:C0521613", "names": ["pancreatic bleeding", "Pancreatic bleeding", "Pancreas hemorrhage", "hemorrhage; pancreas", "Pancreas haemorrhage", "pancreas; hemorrhage", "Pancreatic hemorrhage", "Pancreatic Hemorrhage", "Pancreatic haemorrhage", "Hemorrhage of pancreas", "Haemorrhage of pancreas", "pancreatic bleeding (diagnosis)", "Hemorrhage of pancreas (disorder)", "gastrointestinal bleeding pancreas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemorrhage of pancreas", "shortest_name_length": 19}
{"curie": "UMLS:C4682584", "names": ["Stage IIIA Uterine Corpus Adenosarcoma", "Stage IIIA Uterine Corpus Adenosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Uterine Corpus Adenosarcoma AJCC v8", "shortest_name_length": 38}
{"curie": "MONDO:0043543", "names": ["iatrogenic disease", "Iatrogenic Disease", "Iatrogenic disorder", "iatrogenic disorder", "iatrogenic diseases", "Iatrogenic diseases", "Disease, Iatrogenic", "Iatrogenic Diseases", "disease, iatrogenic", "Diseases, Iatrogenic", "disorders iatrogenic", "diseases, iatrogenic", "Iatrogenic disease, NOS", "Hospital Acquired Condition", "hospital-acquired condition", "hospital acquired condition", "Hospital-Acquired Condition", "hospital-acquired conditions", "Condition, Hospital-Acquired", "Hospital-Acquired Conditions", "condition, hospital-acquired", "conditions, hospital-acquired", "Conditions, Hospital-Acquired", "Iatrogenic disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "iatrogenic disease", "shortest_name_length": 18}
{"curie": "UMLS:C1706698", "names": ["ASCA", "Acidophil Stem Cell Adenoma", "Acidophil Stem Cell PitNET/Adenoma", "Acidophil Stem Cell Pituitary Neuroendocrine Tumor", "Acidophil Stem Cell Pituitary Neuroendocrine Tumor/Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acidophil Stem Cell Pituitary Neuroendocrine Tumor", "shortest_name_length": 4}
{"curie": "UMLS:C5420066", "names": ["Recurrent Intracranial Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Intracranial Neoplasm", "shortest_name_length": 31}
{"curie": "MONDO:0004067", "names": ["gallbladder colloid carcinoma", "Gallbladder Colloid Carcinoma", "gallbladder mucinous carcinoma", "gallbladder colloidal carcinoma", "Gallbladder Colloidal Carcinoma", "Colloid Carcinoma of Gallbladder", "colloid carcinoma of gallbladder", "Mucinous Carcinoma of Gallbladder", "mucinous carcinoma of gallbladder", "colloidal carcinoma of gallbladder", "Colloidal Carcinoma of Gallbladder", "Gallbladder Mucinous Adenocarcinoma", "gallbladder mucinous adenocarcinoma", "gall bladder mucinous adenocarcinoma", "Colloid Carcinoma of the Gallbladder", "colloid carcinoma of the gallbladder", "mucinous carcinoma of the gallbladder", "Mucinous Carcinoma of the Gallbladder", "Colloidal Carcinoma of the Gallbladder", "colloidal carcinoma of the gallbladder", "Colloidal carcinoma of the gallbladder", "mucinous adenocarcinoma of gallbladder", "mucinous adenocarcinoma of gallbladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gallbladder mucinous adenocarcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0800180", "names": ["CPOX-related hereditary coproporphyria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CPOX-related hereditary coproporphyria", "shortest_name_length": 38}
{"curie": "UMLS:C2986680", "names": ["Stage IV Non-Hodgkin Lymphoma", "stage IV childhood non-Hodgkin lymphoma", "Stage IV Childhood Non-Hodgkin Lymphoma", "Ann Arbor Stage IV Childhood Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Childhood Non-Hodgkin Lymphoma", "shortest_name_length": 29}
{"curie": "MONDO:0017833", "names": ["HES-M", "HES-N", "primary HES", "clonal hypereosinophilic syndrome", "primary hypereosinophilic syndrome", "neoplastic hypereosinophilic syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary hypereosinophilic syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0862643", "names": ["Stage IV Prostate Adenocarcinoma", "Adenocarcinoma of the prostate stage IV", "Stage IV Prostate Adenocarcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma of the prostate stage IV", "shortest_name_length": 32}
{"curie": "UMLS:C0275518", "names": ["infection acute", "acute infection", "Acute infection", "acute infections", "Acute infectious disease", "Acute infectious disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute infectious disease", "shortest_name_length": 15}
{"curie": "UMLS:C2347748", "names": ["Erythroleukemia", "adult erythroleukemia", "Adult Erythroleukemia", "adult erythroleukemia (M6a)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Erythroleukemia", "shortest_name_length": 15}
{"curie": "MONDO:0010158", "names": ["T-SUBSTANCE ANOMALY", "T-substance anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-substance anomaly", "shortest_name_length": 19}
{"curie": "MONDO:0019359", "names": ["RMSF", "Choix", "Tobia fever", "Tick typhus", "So Paulo fever", "Fiebre maculosa", "Fiebre manchada", "FIEBRE MANCHADA", "Sao Paulo fever", "FIEBRE MACULOSA", "Sao Paulo typhus", "sao Paulo typhus", "FIEBRE PETEQUIAL", "Sao Paulo; fever", "Fiebre petequial", "Sao Paulo Typhus", "fever; Sao Paulo", "Typhus, Sao Paulo", "Fiebre macuculosa", "Brazillian spotted", "Rocky Mountain fever", "American tick typhus", "Sao Paulo tick typhus", "Brazilian spotted fever", "Brazilian Spotted Fever", "Sao Paulo; spotted fever", "spotted fever; Sao Paulo", "Fever, Brazilian Spotted", "Spotted Fever, Brazilian", "Sao Paulo fever or typhus", "rocky mountain tick fever", "Rocky Mountain tick fever", "Rocky mountain tick fever", "South American tick typhus", "Sao Paulo fever (diagnosis)", "Rocky Mountain spotted fever", "Rocky mountain spotted fever", "rocky spotted mountain fever", "Rocky Mountain Spotted Fever", "ROCKY MOUNTAIN SPOTTED FEVER", "rocky mountain spotted fever", "fever mountain rocky spotted", "Rocky Mountain; spotted fever", "spotted fever; Rocky Mountain", "Rickettsia rickettsii Infection", "Rickettsia rickettsii infection", "Rickettsia rickettsii Infections", "Exanthematic typhus of Sao Paulo", "exanthematic typhus of sao Paulo", "Infection, Rickettsia rickettsii", "RMSF - Rocky Mountain spotted fever", "spotted fever; Rickettsia rickettsii", "rickettsiosis; Rickettsia rickettsii", "Rickettsia; rickettsii, spotted fever", "Rocky Mountain spotted fever (disorder)", "Rocky mountain spotted fever (diagnosis)", "Spotted fever due to Rickettsia rickettsii", "spotted fever due to rickettsia rickettsii", "mountain; fever, Rocky Mountain spotted fever", "fever; mountain, Rocky Mountain spotted fever", "rickettsii; Rickettsia rickettsii, spotted fever", "spotted fever due to rickettsia rickettsii (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rocky mountain spotted fever", "shortest_name_length": 4}
{"curie": "UMLS:C5556684", "names": ["Cervical Mucoepidermoid Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Mucoepidermoid Carcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C1562029", "names": ["breast neoplasm malignant hormone receptor positive", "Hormone receptor positive malignant neoplasm of breast", "Hormone receptor positive malignant neoplasm of breast (disorder)", "Hormone receptor positive malignant neoplasm of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hormone receptor positive malignant neoplasm of breast", "shortest_name_length": 51}
{"curie": "UMLS:C3203548", "names": ["Mycobacterium chelonae infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mycobacterium chelonae infection", "shortest_name_length": 32}
{"curie": "MONDO:0008025", "names": ["HMN2A", "DHMN2A", "HMN 2A", "HMN IIA", "spinal Charcot-Marie-Tooth disease IIA", "Charcot-Marie-Tooth disease, spinal, 2A", "Charcot-Marie-Tooth Disease, Spinal, IIA", "CHARCOT-MARIE-TOOTH DISEASE, SPINAL, IIA", "distal hereditary motor neuropathy type IIA", "HSPB8 neuronopathy, distal hereditary motor", "neuropathy, distal hereditary motor, type 2A", "distal hereditary motor neuronopathy type 2A", "NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IIA", "Neuropathy, Distal Hereditary Motor, Type IIA", "neuronopathy, distal hereditary motor, type 2A", "NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIA", "neuronopathy, distal hereditary motor, type IIA", "Neuronopathy, Distal Hereditary Motor, Type IIA", "autosomal dominant adult spinal muscular atrophy IIA", "Spinal Muscular Atrophy, Distal Adult Autosomal Dominant, IIA", "spinal muscular atrophy, distal, adult, autosomal dominant, 2A", "SPINAL MUSCULAR ATROPHY, DISTAL, ADULT, AUTOSOMAL DOMINANT, IIA", "neuronopathy, distal hereditary motor caused by mutation in HSPB8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuronopathy, distal hereditary motor, type 2A", "shortest_name_length": 5}
{"curie": "UMLS:C0275778", "names": ["lyme carditis", "Lyme carditis", "carditis lymes", "Lyme carditis (disorder)", "Lyme carditis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lyme carditis", "shortest_name_length": 13}
{"curie": "MONDO:0004183", "names": ["Axonal neuropathy", "axonal neuropathy", "Axonal Neuropathy", "axonal neuropathies", "Axonal neuropathy, NOS", "axon peripheral neuropathy", "axonal neuropathy peripheral", "axonal peripheral neuropathy", "peripheral axonal neuropathy", "Axonal peripheral neuropathy", "Axonal neuropathy (disorder)", "Peripheral axonal neuropathy", "peripheral neuropathy of axon", "Peripheral axonal neuropathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "axonal neuropathy", "shortest_name_length": 17}
{"curie": "MONDO:0000395", "names": ["ARBD", "alcohol related birth defect", "Alcohol Related Birth Defect", "alcohol-related birth defect", "alcohol related birth defects", "Alcohol-Related Birth Defects", "Alcohol Related Birth Defects", "alcohol-related birth defects", "Birth Defects, Alcohol-Related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alcohol-related birth defect", "shortest_name_length": 4}
{"curie": "UMLS:C4553415", "names": ["Stage IIB Ovarian Cancer", "Stage IIB Ovarian Cancer AJCC v8", "Stage IIB Ovarian Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Ovarian Cancer AJCC v8", "shortest_name_length": 24}
{"curie": "UMLS:C0920165", "names": ["vascular access complication", "Vascular access complication", "Vascular Access Complication", "Vascular access NOS complication", "vascular access complication (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vascular Access Complication", "shortest_name_length": 28}
{"curie": "MONDO:0016041", "names": ["microgastria", "Microgastria", "congenital microgastria", "Congenital microgastria", "Congenital small stomach", "microgastria (diagnosis)", "Congenital gastric hypoplasia", "Congenital microgastria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital microgastria", "shortest_name_length": 12}
{"curie": "UMLS:C0751339", "names": ["Generalized Myasthenia Gravis", "Myasthenia Gravis, Generalized"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myasthenia Gravis, Generalized", "shortest_name_length": 29}
{"curie": "UMLS:C0242129", "names": ["thrombotic stroke", "THROMBOTIC STROKE", "Thrombotic stroke", "Thrombotic Stroke", "strokes thrombotic", "Stroke, Thrombotic", "Thrombotic Strokes", "stroke - thrombotic", "APOPLEXY, THROMBOTIC", "thrombotic; apoplexy", "thrombosis; apoplexy", "apoplexy; thrombosis", "apoplexy; thrombotic", "Thrombotic stroke (disorder)", "Thrombotic stroke (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thrombotic Stroke", "shortest_name_length": 17}
{"curie": "MONDO:0003678", "names": ["silent MI", "infarction myocardial silent", "MYOCARDIAL INFARCTION SILENT", "Silent Myocardial Infarction", "silent myocardial infarction", "Silent myocardial infarction", "MI - Silent myocardial infarction", "Silent myocardial infarction (disorder)", "silent myocardial infarction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "silent myocardial infarction", "shortest_name_length": 9}
{"curie": "MONDO:0045069", "names": ["Minor Salivary Gland Cancer", "minor salivary gland cancer", "Minor Salivary Gland Carcinoma", "minor salivary gland carcinoma", "Carcinoma of Minor Salivary Gland", "carcinoma of minor salivary gland", "carcinoma of the minor salivary gland", "Carcinoma of the Minor Salivary Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "minor salivary gland carcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C0206247", "names": ["Amyloid neuropathy", "amyloid neuropathy", "Amyloid Neuropathy", "Neuropathy, Amyloid", "amyloid neuropathies", "Amyloid Neuropathies", "Neuropathies, Amyloid", "Amyloid polyneuropathy", "Amyloid Polyneuropathy", "amyloid polyneuropathy", "Polyneuropathy, Amyloid", "Amyloid Polyneuropathies", "Polyneuropathies, Amyloid", "amyloidosis polyneuropathy", "polyneuropathy amyloidosis", "Polyneuropathy in amyloidosis", "Polyneuropathy due to amyloidosis", "amyloid polyneuropathy (diagnosis)", "Polyneuropathy due to amyloidosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Amyloid Neuropathies", "shortest_name_length": 18}
{"curie": "MONDO:0013620", "names": ["CMS16", "congenital myasthenic syndrome 16", "myasthenic syndrome, congenital, 16", "MYASTHENIC SYNDROME, CONGENITAL, 16", "SCN4A congenital myasthenic syndrome", "congenital myasthenic syndrome type 16", "myasthenic syndrome, congenital, type 16", "congenital myasthenic syndrome acetazolamide-responsive", "MYASTHENIC SYNDROME, CONGENITAL, ACETAZOLAMIDE-RESPONSIVE", "myasthenic syndrome, congenital, Acetazolamide-responsive", "congenital myasthenic syndrome caused by mutation in SCN4A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myasthenic syndrome 16", "shortest_name_length": 5}
{"curie": "UMLS:C5206650", "names": ["Primary Peritoneal Clear Cell Carcinoma", "Clear cell adenocarcinoma of peritoneum", "Primary Peritoneal Clear Cell Adenocarcinoma", "Clear cell adenocarcinoma of peritoneum (disorder)", "Clear cell adenocarcinoma of peritoneum (diagnosis)", "peritoneal neoplasm malignant clear cell adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clear cell adenocarcinoma of peritoneum", "shortest_name_length": 39}
{"curie": "UMLS:C1336444", "names": ["stage IV urethra cancer", "Stage IV Urethra Cancer", "Urethra Cancer Stage IV", "stage IV urethral cancer", "Stage IV Urethral Cancer", "stage IV urethra carcinoma", "Stage IV Urethra Carcinoma", "Stage IV Urethral Carcinoma", "stage IV urethral carcinoma", "stage IV carcinoma of urethra", "Stage IV Carcinoma of Urethra", "Stage IV Urethral Cancer AJCC v7", "stage IV urethral cancer AJCC v7", "stage IV carcinoma of the urethra", "Stage IV Carcinoma of the Urethra"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Urethral Cancer AJCC v7", "shortest_name_length": 23}
{"curie": "MONDO:0030326", "names": ["MTDPS16B", "mitochondrial DNA depletion syndrome 16B", "MITOCHONDRIAL DNA DEPLETION SYNDROME 16B (NEUROOPHTHALMIC TYPE)", "mitochondrial DNA depletion syndrome 16B (neuroophthalmic type)", "mitochondrial dna depletion syndrome 16B (neuroophthalmic type)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial dna depletion syndrome 16B (neuroophthalmic type)", "shortest_name_length": 8}
{"curie": "MONDO:0006669", "names": ["be", "Endocarditis bacterial", "ENDOCARDITIS BACTERIAL", "BACTERIAL ENDOCARDITIS", "Bacterial endocarditis", "Infective endocarditis", "Endocarditis infective", "Bacterial Endocarditis", "Endocarditis;bacterial", "bacterial endocarditis", "infective endocarditis", "bacterial; endocarditis", "Endocarditis, bacterial", "Endocarditis, Bacterial", "endocarditis; bacterial", "Bacterial Endocarditides", "Endocarditides, Bacterial", "Endocarditis bacterial NOS", "Endocarditis, infective NOS", "BE - Bacterial endocarditis", "Bacterial endocarditis, NOS", "Bacteria endocarditis (disease)", "bacterial endocarditis (disease)", "Bacterial endocarditis (disorder)", "bacterial endocarditis (diagnosis)", "Bacteria caused endocarditis (disease)", "bacterial infection of the heart valve"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bacterial endocarditis", "shortest_name_length": 2}
{"curie": "MONDO:0005590", "names": ["Duct carcinoma", "Duct Carcinoma", "duct carcinoma", "carcinoma ducts", "Ductal Carcinoma", "carcinoma ducted", "Ductal carcinoma", "carcinoma ductal", "ductal carcinoma", "ductal carcinomas", "carcinomas ductal", "Ductal Carcinomas", "Carcinoma, Ductal", "Carcinomas, Ductal", "Duct carcinoma, NOS", "Duct adenocarcinoma", "Duct cell carcinoma", "Duct Adenocarcinoma", "adenocarcinoma duct", "duct adenocarcinoma", "duct cell carcinoma", "BREAST CANCER DUCTAL", "breast cancer ductal", "ductal breast cancer", "ductal adenocarcinoma", "Ductal adenocarcinoma", "Ductal Adenocarcinoma", "Breast cancer (ductal)", "breast ductal carcinoma", "ductal carcinoma breast", "Ductal Breast Carcinoma", "breast carcinoma ductal", "ductal breast carcinoma", "Breast ductal carcinoma", "Breast Ductal Carcinoma", "carcinoma ductal mammary", "Duct adenocarcinoma, NOS", "mammary ductal carcinoma", "mammary carcinoma ductal", "Carcinoma, Ductal, Breast", "Ductal Carcinoma of Breast", "ductal carcinoma of breast", "carcinoma infiltrating duct", "Infiltrating duct carcinoma", "infiltrating duct carcinoma", "mammary duct adenocarcinoma", "ductal breast adenocarcinoma", "breast ductal adenocarcinoma", "ductal carcinoma of the breast", "Ductal Carcinoma of the Breast", "Infiltrating duct adenocarcinoma", "Infiltrating duct carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast ductal adenocarcinoma", "shortest_name_length": 14}
{"curie": "UMLS:C2931861", "names": ["Hereditary Hematuria Syndrome", "Hemorrhagic Familial Nephritis", "Hematuric Hereditary Nephritis", "Congenital Hereditary Hematuria", "Nephritis, Hematuric Hereditary", "Nephritis, Hemorrhagic Familial", "Hematuria, Congenital Hereditary", "Hemorrhagic Hereditary Nephritis", "Hemorrhagic hereditary nephritis", "Nephritis, Hemorrhagic Hereditary", "Hereditary Familial Congenital Hemorrhagic Nephritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemorrhagic hereditary nephritis", "shortest_name_length": 29}
{"curie": "MONDO:0016713", "names": ["CNS PNET", "central nervous system PNET", "central nervous system primitive neuroectodermal tumor", "Central Nervous System Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor", "central nervous system Ewing sarcoma/peripheral primitive neuroectodermal tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system Ewing sarcoma/peripheral primitive neuroectodermal tumor", "shortest_name_length": 8}
{"curie": "UMLS:C5205652", "names": ["Refractory Anaplastic Ependymoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Anaplastic Ependymoma", "shortest_name_length": 32}
{"curie": "UMLS:C3272803", "names": ["Colorectal Cowden-Associated Polyp"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Cowden-Associated Polyp", "shortest_name_length": 34}
{"curie": "MONDO:0017642", "names": ["intellectual disability-microcephaly-phalangeal-facial abnormalities syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability-microcephaly-phalangeal-facial abnormalities syndrome", "shortest_name_length": 77}
{"curie": "UMLS:C1334976", "names": ["Liver and Intrahepatic Bile Duct Non-Epithelial Neoplasm", "Hepatic and Intrahepatic Bile Duct Non-Epithelial Neoplasm", "Non-Epithelial Hepatic and Intrahepatic Bile Duct Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liver and Intrahepatic Bile Duct Non-Epithelial Neoplasm", "shortest_name_length": 56}
{"curie": "UMLS:C3502107", "names": ["Breastfeeding Jaundice"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breastfeeding Jaundice", "shortest_name_length": 22}
{"curie": "MONDO:0018282", "names": ["dystroglycanopathy", "alpha-dystroglycanopathy", "qualitative or quantitative defects of alpha-dystroglycan"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of alpha-dystroglycan", "shortest_name_length": 18}
{"curie": "UMLS:C4682895", "names": ["Ureter Cancer by AJCC v7 Stage", "Ureter Urothelial Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ureter Cancer by AJCC v7 Stage", "shortest_name_length": 30}
{"curie": "UMLS:C0347521", "names": ["Benign Lacrimal Duct Tumor", "Benign Tumor of Lacrimal Duct", "Benign Lacrimal Duct Neoplasm", "Benign Neoplasm of Lacrimal Duct", "Benign Nasolacrimal Duct Neoplasm", "Benign neoplasm nasolacrimal duct", "Benign Tumor of the Lacrimal Duct", "Benign neoplasm of nasolacrimal duct", "Benign Neoplasm of the Lacrimal Duct", "Benign neoplasm nasolacrimal duct (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Nasolacrimal Duct Neoplasm", "shortest_name_length": 26}
{"curie": "MONDO:0003325", "names": ["GNBn", "Nodular ganglioneuroblastoma", "nodular ganglioneuroblastoma", "Ganglioneuroblastoma, Nodular", "ganglioneuroblastoma, nodular", "Ganglioneuroblastoma, nodular", "Nodular ganglioneuroblastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nodular ganglioneuroblastoma", "shortest_name_length": 4}
{"curie": "MONDO:0014575", "names": ["SGMRT2", "Singleton-Merten syndrome 2", "SINGLETON-MERTEN SYNDROME 2", "singleton-Merten syndrome 2", "singleton-Merten syndrome type 2", "DDX58 singleton-Merten dysplasia", "singleton-Merten dysplasia caused by mutation in DDX58"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Singleton-Merten syndrome 2", "shortest_name_length": 6}
{"curie": "MONDO:0700067", "names": ["FKTN myopathy", "FKTN-related myopathy", "myopathy caused by mutation in FKTN", "myopathy caused by variation in FKTN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy caused by variation in FKTN", "shortest_name_length": 13}
{"curie": "MONDO:0009182", "names": ["JEB-H", "JEB1B", "Herlitz", "Herlitz Disease", "Herlitzs Disease", "JEB-Herlitz type", "Herlitz syndrome", "JEB-HERLITZ TYPE", "Disease, Herlitz", "Herlitz's Disease", "Herlitz' syndrome", "Herlitz's disease", "Disease, Herlitz's", "Severe generalized JEB", "JEB, generalized severe", "Epidermolysis Bullosa Letali", "epidermolysis bullosa letalis", "Epidermolysis bullosa letalis", "Epidermolysis Bullosa Letalis", "EPIDERMOLYSIS BULLOSA LETALIS", "Bullosa Letali, Epidermolysis", "Letali, Epidermolysis Bullosa", "Bullosa Letalis, Epidermolysis", "Letalis, Epidermolysis Bullosa", "epidermolysis; bullosa, letalis", "bullosa; epidermolysis, letalis", "Lethal Junctional Epidermolysis Bullosa", "Epidermolysis bullosa hereditaria letalis", "epidermolysis bullosa letalis (diagnosis)", "Herlitz Pearson Type Epidermolysis Bullosa", "Herlitz-Pearson Type Epidermolysis Bullosa", "HERLITZ-PEARSON-TYPE EPIDERMOLYSIS BULLOSA", "Herlitz-Pearson type epidermolysis bullosa", "Herlitz-Pearson-Type Epidermolysis Bullosa", "Herlitz-Pearson-type epidermolysis bullosa", "Bullosa, Herlitz-Pearson-Type Epidermolysis", "Epidermolysis Bullosa, Herlitz-Pearson-Type", "EPIDERMOLYSIS BULLOSA, JUNCTIONAL 1B, SEVERE", "junctional epidermolysis bullosa Herlitz type", "Junctional epidermolysis bullosa, Herlitz type", "junctional epidermolysis bullosa, Herlitz type", "Epidermolysis Bullosa, Junctional, Herlitz Type", "epidermolysis bullosa, junctional, Herlitz type", "Herlitz type epidermolysis bullosa junctionalis", "EPIDERMOLYSIS BULLOSA, JUNCTIONAL, HERLITZ TYPE", "Epidermolysis Bullosa Junctionalis, Herlitz Type", "EPIDERMOLYSIS BULLOSA JUNCTIONALIS, HERLITZ TYPE", "epidermolysis bullosa Junctionalis, Herlitz type", "Junctional epidermolysis bullosa gravis of Herlitz", "Severe generalized junctional epidermolysis bullosa", "junctional epidermolysis bullosa, generalized severe", "Junctional epidermolysis bullosa generalisata gravis", "junctional epidermolysis bullosa generalisata gravis", "EPIDERMOLYSIS BULLOSA, JUNCTIONAL, GENERALIZED SEVERE", "junctional epidermolysis bullosa, Herlitz-Pearson type", "Junctional epidermolysis bullosa, lethal type, Herlitz", "Epidermolysis bullosa, junctional Herlitz-Pearson type", "Junctional epidermolysis bullosa, Herlitz-Pearson type", "EPIDERMOLYSIS BULLOSA, JUNCTIONAL, HERLITZ-PEARSON TYPE", "Epidermolysis Bullosa, Junctional, Herlitz-Pearson Type", "epidermolysis bullosa, junctional, Herlitz-Pearson type", "Junctional epidermolysis bullosa gravis of Herlitz (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "junctional epidermolysis bullosa Herlitz type", "shortest_name_length": 5}
{"curie": "UMLS:C4725612", "names": ["Refractory Ovarian Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Ovarian Carcinoma", "shortest_name_length": 28}
{"curie": "UMLS:C2945767", "names": ["hepatoma, childhood", "hepatoma, pediatric", "Pediatric Liver Cancer", "liver cancer pediatric", "childhood liver cancer", "pediatric liver cancer", "Childhood Liver Cancer", "liver cancer, pediatric", "liver cancer, childhood", "Malignant Liver Neoplasm", "Childhood Cancer of Liver", "Pediatric Cancer of Liver", "Liver cancer, child primary", "Pediatric Cancer of the Liver", "Childhood Cancer of the Liver", "Childhood Malignant Liver Tumor", "Childhood Malignant Liver Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Malignant Liver Neoplasm", "shortest_name_length": 19}
{"curie": "MONDO:0010183", "names": ["cblF", "MAHCF", "CblF defect", "cblF defect", "cobalamin F defect", "Cobalamin F defect", "COBALAMIN F DISEASE", "Cobalamin F Disease", "cobalamin F disease", "Cobalamin F deficiency", "cobalamin F deficiency", "cobalamin locus f variant", "Cobalamin locus F variant", "Vitamin B12 Storage Disease", "vitamin B12 storage disease", "VITAMIN B12 STORAGE DISEASE", "CblF - Cobalamin locus F variant", "Vitamin B12 Lysosomal Release Defect", "vitamin B12 lysosomal release defect", "VITAMIN B12 LYSOSOMAL RELEASE DEFECT", "COBALAMIN, DEFECT IN LYSOSOMAL RELEASE OF", "Cobalamin, Defect in Lysosomal Release of", "cobalamin, defect in lysosomal release of", "cblF methylmalonic acidemia and homocystinuria", "CblF methylmalonic acidemia and homocystinuria", "CblF methylmalonic acidaemia and homocystinuria", "Inherited methylmalonic acidemia AND homocystinuria", "Inherited methylmalonic acidemia and homocystinuria", "lysosomal membrane cobalamin transporter deficiency", "methylmalonic aciduria and homocystinuria type cblF", "Lysosomal membrane cobalamin transporter deficiency", "inherited methylmalonic acidemia and homocystinuria", "Methylmalonic acidemia with homocystinuria type cblF", "methylmalonic aciduria and homocystinuria, cblF type", "Methylmalonic Acidemia and Homocystinuria, CblF Type", "Methylmalonic Aciduria and Homocystinuria, cblF Type", "METHYLMALONIC ACIDEMIA AND HOMOCYSTINURIA, cblF TYPE", "Inherited methylmalonic acidaemia AND homocystinuria", "methylmalonic acidemia and homocystinuria, cblF type", "METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblF TYPE", "Methylmalonic Aciduria and Homocystinuria, CblF Type", "methylmalonic acidemia with homocystinuria type cblF", "Methylmalonic aciduria with homocystinuria, type cblF", "methylmalonic aciduria with homocystinuria, type cblF", "Adenosylcobalamin and methylcobalamin synthesis defect", "adenosylcobalamin and methylcobalamin synthesis defect", "METHYLMALONIC ACIDURIA DUE TO VITAMIN B12-RELEASE DEFECT", "methylmalonic aciduria due to vitamin B12-release defect", "Methylmalonic Aciduria due to Vitamin B12-Release Defect", "Adenosylcobalamin and methylcobalamin synthesis defect, NOS", "Inherited methylmalonic acidemia AND homocystinuria (disorder)", "Adenosylcobalamin and methylcobalamin synthesis defect (disorder)", "adenosylcobalamin and methylcobalamin synthesis defect (diagnosis)", "combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblF", "Combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblF", "Combined methylmalonic acidemia and homocystinuria due to defects in adenosylcobalamin and methylcobalamin synthesis", "Combined methylmalonic acidaemia and homocystinuria due to defects in adenosylcobalamin and methylcobalamin synthesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "methylmalonic aciduria and homocystinuria type cblF", "shortest_name_length": 4}
{"curie": "MONDO:0009269", "names": ["GPHYSD1", "GELEOPHYSIC dysplasia 1", "geleophysic dysplasia 1", "GELEOPHYSIC DYSPLASIA 1", "Geleophysic dysplasia type 1", "ADAMTSL2 geleophysic dysplasia", "geleophysic dysplasia caused by mutation in ADAMTSL2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "geleophysic dysplasia 1", "shortest_name_length": 7}
{"curie": "MONDO:0045045", "names": ["igg deficiency", "IgG deficiency", "IgG Deficiency", "Deficiency, IgG", "IgG Deficiencies", "igg deficiencies", "Deficiencies, IgG", "igg subclass deficiency", "IgG subclass deficiency", "IgG Deficiency disorder", "IGG SUBCLASS DEFICIENCY", "selective IgG deficiency", "deficiencies igg subclass", "IgG deficiency (diagnosis)", "Selective deficiency of IgG", "Immunoglobulin G deficiency", "Selective IgG immunodeficiency", "selective IgG immunodeficiency", "Selective IgG Immunodeficiency", "Selective IgG subclass deficiency", "selective IgG deficiency (diagnosis)", "Immunoglobulin G subclass deficiency", "Selective immunoglobulin G deficiency", "Immunoglobulin G deficiency (disorder)", "Selective Immunoglobulin G Subclass Deficiency", "Selective immunoglobulin G deficiency (disorder)", "immunodeficiency disorders immunoglobulin g deficiency", "Selective deficiency of immunoglobulin G [IgG] subclasses"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "selective IgG immunodeficiency", "shortest_name_length": 14}
{"curie": "MONDO:0002347", "names": ["barbiturate dependence", "Barbiturate dependence", "Barbiturate dependency", "dependence; barbiturate(s)", "barbiturate(s); dependence", "Dependence on barbiturates", "Barbiturate dependence (disorder)", "barbiturate dependence (diagnosis)", "Drug dependence of barbiturate type", "Sedative, hypnotic or anxiolytic dependence, continuous", "Barbiturate and similarly acting sedative or hypnotic dependence, continuous use"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "barbiturate dependence", "shortest_name_length": 22}
{"curie": "MONDO:0012155", "names": ["PCA", "atresia; nares", "nares; atresia", "choana; atresia", "choanal; fusion", "choanal atresia", "atresia; choana", "fusion; choanal", "Choanal atresia", "atresia choanal", "Choanal Atresia", "Atresia of nares", "Atresia, Choanal", "Choanal Atresias", "atresia of nares", "Imperforate nares", "Atresias, Choanal", "imperforate nares", "posterior choanal atresia", "choanal atresia, POSTERIOR", "Atresia of posterior naris", "Choanal atresia (disorder)", "Atresia of posterior nares", "Choanal Atresia, Posterior", "CHOANAL ATRESIA, POSTERIOR", "choanal atresia (diagnosis)", "Congenital atresia of choana", "choanal atresia (physical finding)", "Congenital atresia of posterior nares", "Blockage of the rear opening of the nasal cavity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choanal atresia", "shortest_name_length": 3}
{"curie": "MONDO:0014936", "names": ["ZTTKS", "TOKIMS", "ZTTK SYNDROME", "ZTTK syndrome", "Tokita-Kim syndrome", "Zhu Tokita Takenouchi Kim syndrome", "ZHU-TOKITA-TAKENOUCHI-KIM SYNDROME", "Zhu-Tokita-Takenouchi-Kim syndrome", "ZTTK MULTIPLE CONGENITAL ANOMALIES-MENTAL RETARDATION SYNDROME", "ZTTK multiple congenital anomalies-mental retardation syndrome", "ZTTK multiple congenital anomalies-intellectual disability syndrome", "brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome", "Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome", "Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome", "Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ZTTK syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0014839", "names": ["COCPMR", "chorea, childhood-onset, with psychomotor retardation", "CHOREA, CHILDHOOD-ONSET, WITH PSYCHOMOTOR RETARDATION", "chorea, childhood-onset, with psychomotor retardation; COCPMR"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chorea, childhood-onset, with psychomotor retardation", "shortest_name_length": 6}
{"curie": "UMLS:C0175816", "names": ["CAS", "CAD", "cAHA", "cAIHA", "Cold AIHA", "Cold Antibody Disease", "Cold Antibody Diseases", "Cold hemolytic disease", "Cold Agglutinin Disease", "Cold haemolytic disease", "Cold agglutinin disease", "cold agglutinin disease", "Cold agglutinin syndrome", "Agglutinin Disease, Cold", "agglutinins cold disease", "Cold Agglutinin Diseases", "cold hemagglutinin disease", "Cold hemagglutinin disease", "Cold type hemolytic anemia", "hemolytic anemia cold type", "Cold Hemagglutinin Disease", "Cryopathic hemolytic anemia", "Cold haemagglutinin disease", "Cold type haemolytic anaemia", "Cryopathic haemolytic anaemia", "Cold Antibody Hemolytic Anemia", "Cold antibody hemolytic anemia", "cold antibody hemolytic anemia", "Chronic cold agglutinin disease", "cold autoimmune hemolytic anemia", "Anemia, Hemolytic, Cold Antibody", "Cold antibody haemolytic anaemia", "Cold autoimmune hemolytic anemia", "CHAD - Cold hemagglutinin disease", "Cold autoimmune haemolytic anaemia", "CHAD - Cold haemagglutinin disease", "Hemolytic anemia due to cold antibody", "Autoimmune hemolytic anemia, cold type", "CRYOPATHIC AUTOIMMUNE HEMOLYTIC ANEMIA", "AIHA - Cold autoimmune hemolytic anemia", "Haemolytic anaemia due to cold antibody", "AIHA - Cold autoimmune haemolytic anaemia", "Hemolytic anemia due to cold antibody, NOS", "Cold autoimmune hemolytic anemia (disorder)", "Haemolytic anaemia due to cold antibody, NOS", "hemolytic anemia due to cold agglutinin disease", "Autoimmune hemolytic anemia, cold antibody type", "anemia hemolytic acquired cold agglutinin disease", "hemolytic anemia due to cold agglutinin disease (diagnosis)", "Cold type (primary) (secondary) (symptomatic) autoimmune hemolytic anemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cold Hemagglutinin Disease", "shortest_name_length": 3}
{"curie": "UMLS:C4527167", "names": ["Stage IIA Cutaneous (Skin) Melanoma", "Clinical Stage IIA Cutaneous Melanoma AJCC v8", "Clinical Stage IIA Melanoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage IIA Cutaneous Melanoma AJCC v8", "shortest_name_length": 35}
{"curie": "MONDO:0014982", "names": ["MYP25", "P4HA2 myopia (disease)", "myopia 25, autosomal dominant", "MYOPIA 25, AUTOSOMAL DOMINANT", "myopia 25, autosomal dominant; MYP25", "myopia (disease) caused by mutation in P4HA2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopia 25, autosomal dominant", "shortest_name_length": 5}
{"curie": "MONDO:0024472", "names": ["Kenya fever", "Marseilles fever", "marseilles fever", "boutonneuse fever", "BOUTONNEUSE FEVER", "Marseilles; fever", "fever; Marseilles", "Kenya tick typhus", "Boutonneuse Fever", "kenya tick typhus", "Boutonneuse fever", "Kenyan tick typhus", "Fievre boutonneuse", "fievre boutonneuse", "fièvre boutonneuse", "FEVER, BOUTONNEUSE", "Fever, Boutonneuse", "Boutonneuse Fevers", "African tick typhus", "Fevers, Boutonneuse", "boutonneuse disease", "Boutonneuse disease", "Mediterranean tick fever", "tick fever; mediterranean", "Conor and Bruch's disease", "FEVER, MEDITERRANEAN TICK", "mediterranean; tick fever", "mediterranean spotted fever", "Mediterranean spotted fever", "Mediterranean Spotted Fever", "Boutonneuse fever (disorder)", "mediterranean; spotted fever", "Spotted Fever, Mediterranean", "Rickettsia conorii infection", "Rickettsia conorii Infection", "spotted fever; mediterranean", "Infection, Rickettsia conorii", "boutonneuse fever (diagnosis)", "Rickettsia conorii Infections", "South African tick-bite fever", "Infections, Rickettsia conorii", "Rickettsia conorii spotted fever", "spotted fever; Rickettsia conorii", "Rickettsia; conorii, spotted fever", "Tick typhus due to Rickettsia conorii", "tick typhus due to rickettsia conorii", "spotted fever due to Rickettsia conorii", "Spotted fever due to Rickettsia conorii", "conorii; Rickettsia conorii, spotted fever", "TICK-BORNE RICKETTSIOSIS, EASTERN HEMISPHERE", "spotted fever due to Rickettsia conorii (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "boutonneuse fever", "shortest_name_length": 11}
{"curie": "UMLS:C1332872", "names": ["Cellular Precursor of Cancer", "Precancerous Cellular Change"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cellular Precursor of Cancer", "shortest_name_length": 28}
{"curie": "MONDO:0018090", "names": ["DOLV", "double outlet left ventricle", "Double-outlet left ventricle", "Double outlet left ventricle", "outlet; double left ventricle", "ventricle; double outlet left", "double; outlet, left ventricle", "ventricle; left, double outlet", "double outlet of left ventricle", "DOLV - Double outlet left ventricle", "double outlet left ventricle (disease)", "Double outlet left ventricle (disorder)", "double outlet from morphologic LV chamber", "double outlet of left ventricle (diagnosis)", "Origin of both great vessels from left ventricle", "double outlet from morphologic left ventricular chamber", "double outlet from morphologic left ventricular chamber (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "double outlet left ventricle", "shortest_name_length": 4}
{"curie": "UMLS:C0238132", "names": ["Bronchopleural fistula", "bronchopleural fistula", "Bronchopleural Fistula", "fistula; bronchopleural", "Fistula, bronchopleural", "FISTULA, BRONCHOPLEURAL", "bronchopleural; fistula", "Bronchopleural fistula (disorder)", "bronchopleural fistula (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bronchopleural Fistula", "shortest_name_length": 22}
{"curie": "UMLS:C1608950", "names": ["Device dislocation", "Device dislodgement", "Device septum dislodgement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Device dislocation", "shortest_name_length": 18}
{"curie": "MONDO:0003469", "names": ["Epithelial Synovial Sarcoma", "epithelial synovial sarcoma", "epithelioid Synovial sarcoma", "Epithelioid Synovial Sarcoma", "epithelioid synovial sarcoma", "Epithelial Sarcoma of Synovium", "epithelial sarcoma of synovium", "Epithelioid Cell Synovial Sarcoma", "synovial epithelioid cell sarcoma", "epithelioid cell synovial sarcoma", "epithelial sarcoma of the synovium", "Epithelial Sarcoma of the Synovium", "Synovial sarcoma, epithelioid cell", "synovial sarcoma, epithelioid cell", "Synovial sarcoma - epithelioid cell", "Epithelioid Cell Sarcoma of Synovium", "epithelioid cell sarcoma of synovium", "Synovial sarcoma, epithelioid cell type", "epithelioid cell sarcoma of the synovium", "Epithelioid Cell Sarcoma of the Synovium", "epithelioid cell synovial sarcoma (diagnosis)", "Synovial sarcoma, epithelioid cell (morphologic abnormality)", "synovial sarcoma, epithelioid cell (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epithelioid cell synovial sarcoma", "shortest_name_length": 27}
{"curie": "MONDO:0100286", "names": ["RSV bronchiolitis", "respiratory syncytial virus bronchiolitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "respiratory syncytial virus bronchiolitis", "shortest_name_length": 17}
{"curie": "MONDO:0004910", "names": ["mvp", "MVP", "HEART, SOLDIER", "Click syndrome", "click syndrome", "Mitral prolapse", "BARLOW SYNDROME", "mitral; prolapse", "prolapse; mitral", "barlow's syndrome", "Barlow's syndrome", "Floppy Mitral Valve", "Floppy mitral valve", "floppy mitral valve", "Floppy Mitral Valves", "Mitral Valve, Floppy", "mitral valve; floppy", "J.B. Barlow syndrome", "MITRAL VALVE PROLAPSE", "Prolapse;mitral valve", "Click Murmur Syndrome", "Mitral Valve Prolapse", "Click-murmur syndrome", "Floppy valve syndrome", "CLICK MURMUR SYNDROME", "Mitral Valves, Floppy", "floppy valve syndrome", "mitral valve prolapse", "Click-Murmur Syndrome", "click-murmur syndrome", "Mitral valve prolapse", "prolapse, mitral valve", "Syndrome, Click-Murmur", "Valve Prolapse, Mitral", "Mitral Valve Prolapses", "Click-Murmur Syndromes", "J.B. Barlow's syndrome", "Prolapsed mitral valve", "Prolapse, Mitral Valve", "Mitral valve prolapsed", "Prolapsed Mitral Valve", "Valve, Prolapsed Mitral", "Prolapses, Mitral Valve", "Prolapsed Mitral Valves", "Syndromes, Click-Murmur", "Mitral leaflet prolapse", "Mitral Valve, Prolapsed", "Valve Prolapses, Mitral", "mitral leaflet syndrome", "Mitral (valve) prolapse", "Mitral Valves, Prolapsed", "Valves, Prolapsed Mitral", "valve, prolapse Of mitral", "MVP - Mitral valve prolapse", "mitral valve prolapse (MVP)", "MITRAL CLICK-MURMUR SYNDROME", "Mitral Click-Murmur Syndrome", "floppy mitral valve syndrome", "Mitral Click Murmur Syndrome", "Click-Murmur Syndrome, Mitral", "Syndrome, Mitral Click-Murmur", "Mitral valve prolapse syndrome", "mitral valve prolapse syndrome", "Systolic Click-Murmur Syndrome", "SYSTOLIC MURMUR-CLICK SYNDROME", "Mitral Valve Prolapse Syndrome", "systolic click-murmur syndrome", "syndrome; floppy, mitral valve", "Systolic Click Murmur Syndrome", "MITRAL VALVE PROLAPSE SYNDROME", "floppy; syndrome, mitral valve", "Syndrome, Systolic Click-Murmur", "Click-Murmur Syndrome, Systolic", "mitral valve prolapse (disease)", "myxomatous mitral valve prolapse", "Mitral valve prolapse (disorder)", "mitral valve prolapse (diagnosis)", "mitral valve prolapse, myxomatous", "J.B. Barlow's syndrome (diagnosis)", "Asynchronous valve closure syndrome", "mitral; floppy mitral valve syndrome", "syndrome; floppy mitral valve syndrome", "Mitral regurgitation due to cusp prolapse", "Mitral valve prolapse syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitral valve prolapse", "shortest_name_length": 3}
{"curie": "UMLS:C4683660", "names": ["Diffuse Large B-Cell Lymphoma by Ann Arbor Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse Large B-Cell Lymphoma by Ann Arbor Stage", "shortest_name_length": 48}
{"curie": "MONDO:0014581", "names": ["CMS2A", "SCCMS", "CMS IIa", "congenital myasthenic syndrome 2A", "congenital myasthenic syndrome type 2A", "myasthenic syndrome, congenital, type IIa", "slow channel congenital myasthenic syndrome", "myasthenic syndrome, congenital, slow-channel", "congenital myasthenic syndrome 2A slow-channel", "MYASTHENIC SYNDROME, CONGENITAL, 2A, SLOW-CHANNEL", "myasthenic syndrome, congenital, 2A, slow-channel", "myasthenic syndrome, congenital, postsynaptic slow-channel"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myasthenic syndrome 2A", "shortest_name_length": 5}
{"curie": "MONDO:0019073", "names": ["HLTRS", "HLT-renal defect syndrome", "Glomerulonephritis sparse hair telangiectases", "Glomerulonephritis With Sparse Hair And Telangiectases", "GLOMERULONEPHRITIS WITH SPARSE HAIR AND TELANGIECTASES", "glomerulonephritis with sparse hair and telangiectases", "Telangiectatic membranoproliferative glomerulonephritis", "TELANGIECTATIC MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS", "telangiectatic membranoproliferative glomerulonephritis", "Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome", "HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME", "hypotrichosis-lymphedema-telangiectasia-renal defect syndrome", "Hypotrichosis, lymphedema, telangiectasia, renal defect syndrome", "Hypotrichosis, lymphoedema, telangiectasia, renal defect syndrome", "HLTRS (hypotrichosis, lymphedema, telangiectasia, renal defect) syndrome", "HLTRS (hypotrichosis, lymphoedema, telangiectasia, renal defect) syndrome", "Hypotrichosis, lymphedema, telangiectasia, renal defect syndrome (disorder)", "Cutaneous telangiectasia, sparse hair and membranoproliferative glomerulonephritis", "hypotrichosis-lymphedema-telangiectasia-membranoproliferative glomerulonephritis syndrome", "Hypotrichosis-lymphedema-telangiectasia-membranoproliferative glomerulonephritis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotrichosis-lymphedema-telangiectasia-renal defect syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0011118", "names": ["Acute Bilineal Leukemia", "acute bilineal leukemia", "Acute bilineal leukemia", "bilineal acute leukemia", "Acute bilineal leukaemia", "bilineal acute myeloid leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bilineal acute myeloid leukemia", "shortest_name_length": 23}
{"curie": "MONDO:0011738", "names": ["BFPP", "bilateral frontoparietal polymicrogyria", "Bilateral Frontoparietal Polymicrogyria", "Bilateral frontoparietal polymicrogyria", "POLYMICROGYRIA, BILATERAL FRONTOPARIETAL", "Polymicrogyria, Bilateral Frontoparietal", "polymicrogyria, bilateral frontoparietal", "BFPP - bilateral frontoparietal polymicrogyria", "CEREBELLAR ATAXIA WITH NEURONAL MIGRATION DEFECT", "Cerebellar Ataxia with Neuronal Migration Defect", "cerebellar ataxia with neuronal migration defect", "Bilateral frontoparietal polymicrogyria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bilateral frontoparietal polymicrogyria", "shortest_name_length": 4}
{"curie": "UMLS:C0235746", "names": ["SALIVA ALTERED", "Altered saliva", "Saliva altered"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Saliva altered", "shortest_name_length": 14}
{"curie": "UMLS:C5419514", "names": ["Locally Advanced Sarcomatoid Renal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Sarcomatoid Renal Cell Carcinoma", "shortest_name_length": 49}
{"curie": "UMLS:C0854825", "names": ["Anaplastic Large Cell Lymphoma Stage IV", "Stage IV Anaplastic Large Cell Lymphoma", "Ann Arbor Stage IV Anaplastic Large Cell Lymphoma", "Anaplastic large cell lymphoma T- and null-cell types stage IV", "Ann Arbor Stage IV Noncutaneous Anaplastic Large Cell Lymphoma", "Anaplastic Large Cell Lymphoma T- and Null-Cell Types Stage IV"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Anaplastic Large Cell Lymphoma", "shortest_name_length": 39}
{"curie": "UMLS:C3897237", "names": ["Untreated Anaplastic Oligodendroglioma", "Untreated Childhood Anaplastic Oligodendroglioma", "untreated childhood anaplastic oligodendroglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Untreated Childhood Anaplastic Oligodendroglioma", "shortest_name_length": 38}
{"curie": "MONDO:0024361", "names": ["Sleep rhythm problem", "Circadian Dysregulation", "Circadian dysregulation", "circadian sleep disorder", "Dysregulation, Circadian", "Sleep-Wake Cycle Disorder", "Circadian Rhythm Disorder", "Sleep Wake Cycle Disorder", "circadian rhythm disorder", "Circadian Rhythm Disorders", "Sleep-Wake Cycle Disorders", "circadian rhythm disorders", "Sleep Wake Cycle Disorders", "Sleep-Wake Schedule Disorder", "sleep wake schedule disorder", "Disorder of sleep-wake cycle", "Sleep Wake Schedule Disorder", "sleep-wake schedule disorder", "Sleep-wake schedule disorder", "Disturbed nyctohemeral rhythm", "Disturbed Nyctohemeral Rhythm", "Sleep-Wake Schedule Disorders", "Sleep Wake Schedule Disorders", "Disturbed Nyctohemeral Rhythms", "Nyctohemeral Rhythm, Disturbed", "Disorder of sleep-wake schedule", "Circadian rhythm sleep disorder", "circadian rhythm sleep disorder", "Nyctohemeral Rhythms, Disturbed", "sleep disorder circadian rhythm", "Circadian Rhythm Sleep Disorder", "circadian rhythm; sleep disorder", "sleep disorder; circadian rhythm", "Circadian rhythm sleep disorders", "Circadian Rhythm Sleep Disorders", "Sleep wake schedule disorder NOS", "circadian rhythm sleep disorders", "Sleep-wake schedule disorder, NOS", "Sleep Disorders, Circadian Rhythm", "Disorders of the sleep-wake schedule", "Circadian rhythm sleep disorder, NOS", "Circadian rhythm sleep-wake disorder", "disorders of the sleep-wake schedule", "Disorders of the sleep wake schedule", "Disorder of sleep-wake cycle (disorder)", "circadian rhythm sleep disorder (diagnosis)", "sleep-wake pattern or schedule; sleep disorder", "sleep disorder; sleep-wake pattern or schedule"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "circadian rhythm sleep disorder", "shortest_name_length": 20}
{"curie": "UMLS:C0037367", "names": ["Smoke inhalation", "INHALATION SMOKE", "inhalation smoke", "Smoke Inhalation", "Inhalation;smoke", "smoke inhalation", "Smoke inhalation NOS", "Smoke inhalation injury", "smoke inhalation injury", "Smoke Inhalation Injury", "Injury, Smoke Inhalation", "Inhalation Injury, Smoke", "smoke inhalation injuries", "Smoke Inhalation Injuries", "Injuries, Smoke Inhalation", "Inhalation Injuries, Smoke", "Smoke inhalation injury (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Smoke Inhalation Injury", "shortest_name_length": 16}
{"curie": "UMLS:C1336112", "names": ["Stage IA Bone Sarcoma", "Stage IA Sarcoma of Bone", "Stage IA Sarcoma of the Bone", "Stage IA Bone Sarcoma AJCC v7", "Stage IA Bone Sarcoma  AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Bone Sarcoma AJCC v7", "shortest_name_length": 21}
{"curie": "UMLS:C5420167", "names": ["Pharyngeal Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pharyngeal Non-Hodgkin Lymphoma", "shortest_name_length": 31}
{"curie": "UMLS:C0158940", "names": ["TTN", "Wet lung syndrome", "Wet Lung Syndrome", "wet lung syndrome", "Retained Fetal Lung Fluid", "Wet-lung disease of newborn", "Newborn Transient Tachypnea", "transient newborn tachypnea", "transient tachypnea newborn", "newborn tachypnea transient", "Wet lung disease of newborn", "Newborn transitory tachypnea", "Tachypnoea;transient;newborn", "Wet lung syndrome in newborn", "transient newborn tachypnoea", "Newborn Transient Tachypneas", "TACHYPNEA, TRANSIENT, NEWBORN", "Newborn transitory tachypnoea", "Transient tachypnea of newborn", "transient tachypnea of newborn", "Transient Tachypnea of Newborn", "Transitory Tachypnea of Newborn", "Idiopathic tachypnea of newborn", "Transient tachypnoea of newborn", "Transitory tachypnea of newborn", "Transitory tachypnoea of newborn", "Idiopathic tachypnoea of newborn", "Transient Tachypnea of the Newborn", "Transient tachypnea of the newborn", "Transient tachypnoea of the newborn", "TTN - Transient tachypnea of newborn", "RESPIRATORY DISTRESS SYNDROME TYPE II", "TTN - Transient tachypnoea of newborn", "Type II Respiratory Distress Syndrome", "Respiratory distress syndrome, type II", "rapid; respiratory, transient, of newborn", "respiration; rapid, transient, of newborn", "transient tachypnea of newborn (diagnosis)", "Transitory tachypnea of newborn (disorder)", "Tachypnea resolving about 6 hours postnatally", "Tachypnoea resolving about 6 hours postnatally"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transitory tachypnea of newborn", "shortest_name_length": 3}
{"curie": "MONDO:0044338", "names": ["Autoimmune primary ovarian failure", "autoimmune primary ovarian failure", "Autoimmune primary ovarian failure (disorder)", "primary ovarian failure arising through autoimmunity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune primary ovarian failure", "shortest_name_length": 34}
{"curie": "MONDO:0015079", "names": ["multiple polyglandular tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple polyglandular tumor", "shortest_name_length": 28}
{"curie": "MONDO:0016733", "names": ["Glioneuroma", "glioneuroma", "Ganglioglioma", "ganglioglioma", "gangliogliomas", "Gangliogliomas", "Neuroastrocytoma", "neuroastrocytoma", "CNS ganglioglioma", "Ganglioglioma, NOS", "Adult Ganglioglioma", "adult ganglioglioma", "Childhood Ganglioglioma", "childhood ganglioglioma", "Ganglioglioma (disorder)", "Ganglioglioma (morphologic abnormality)", "mixed cell tumors containing both neural ganglionic cells and neural glial cell components"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ganglioglioma", "shortest_name_length": 11}
{"curie": "MONDO:0010306", "names": ["MRSS", "MRXSC", "MRXS15", "Cabezas syndrome", "Cabezas Syndrome", "CABEZAS SYNDROME", "mental retardation, X-linked, syndromic 15", "Mental Retardation, X-Linked, Syndromic 15", "MENTAL RETARDATION, X-LINKED, SYNDROMIC 15", "Cabezas X-Linked Mental Retardation Syndrome", "X-linked intellectual disability Cabezas type", "Cul4B-related X-linked intellectual disability", "X-linked mental retardation with short stature", "X-linked intellectual disability, Cabezas type", "intellectual disability, X-linked, syndromic 15", "mental retardation, X-linked, with short stature", "MENTAL RETARDATION, X-LINKED, WITH SHORT STATURE", "Mental Retardation, X-Linked, with Short Stature", "X-linked intellectual disability with short stature", "MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE", "intellectual disability, X-linked, with short stature", "mental retardation, X-linked, syndromic, Cabezas type", "Mental Retardation, X-Linked, Syndromic, Cabezas Type", "syndromic X-linked intellectual disability Cabezas type", "X-linked intellectual disability Cabezas type (disorder)", "mental retardation, X-linked, syndromic 15 (Cabezas type)", "X-linked intellectual disability Cabezas type (diagnosis)", "Cabezas type of X-linked syndromic intellectual disability", "intellectual disability, X-linked, syndromic, Cabezas type", "Cabezas syndrome; syndromic X-linked mental retardation 15", "intellectual disability, X-linked, syndromic 15 (Cabezas type)", "Cabezas syndrome; syndromic X-linked intellectual disability 15", "Mental Retardation, X-Linked, With Brachydactyly And Macroglossia", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CABEZAS TYPE", "mental retardation, X-linked, syndromic 15 (Cabezas type), X-linked recessive", "X-linked mental retardation with short stature, hypogonadism, and abnormal gait", "Mental Retardation, X-Linked, with Short Stature, Hypogonadism, and Abnormal Gait", "MENTAL RETARDATION, X-LINKED, WITH SHORT STATURE, HYPOGONADISM, AND ABNORMAL GAIT", "mental retardation, X-linked, with short stature, hypogonadism, and abnormal Gait", "X-linked intellectual disability with short stature, hypogonadism, and abnormal gait", "intellectual disability, X-linked, with short stature, hypogonadism, and abnormal Gait", "Mental Retardation, X-Linked, With Short Stature, Small Testes, Muscle Wasting, And Tremor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability, Cabezas type", "shortest_name_length": 4}
{"curie": "UMLS:C0454560", "names": ["Acquired language disorder", "Acquired Language Disorder", "Language Disorder, Acquired", "Acquired Language Disorders", "Language Disorders, Acquired", "Acquired language disorder (disorder)", "Acquired language disorder (diagnosis)", "communication disorder acquired language"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired Language Disorders", "shortest_name_length": 26}
{"curie": "UMLS:C0333233", "names": ["Active Hyperemia", "Active hyperemia", "Hyperemia, active", "Active hyperaemia", "Hyperemia, Active", "Active congestion", "Arterial Hyperemia", "Congestion, active", "Hyperemia, Arterial", "Active congestion (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Active Hyperemia", "shortest_name_length": 16}
{"curie": "MONDO:0018131", "names": ["Del(9)(q21)", "9q21 microdeletion syndrome", "neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome due to 9q21 microdeletion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome due to 9q21 microdeletion", "shortest_name_length": 11}
{"curie": "UMLS:C0279646", "names": ["Acute Monocytic Leukemia", "Pediatric Acute M5b Leukemia", "childhood acute M5b leukemia", "pediatric acute M5b leukemia", "Childhood Acute M5b Leukemia", "M5b leukemia, childhood acute", "pediatric AMOL, differentiated", "childhood AMOL, differentiated", "Childhood Acute Monocytic Leukemia", "M5b childhood AMOL, differentiated", "childhood acute monocytic leukemia (M5b)", "pediatric acute differentiated monocytic leukemia", "Pediatric Acute Differentiated Monocytic Leukemia", "M5b Childhood Acute Differentiated Monocytic Leukemia", "M5b Pediatric Acute Differentiated Monocytic Leukemia", "childhood acute differentiated monocytic leukemia (M5b)", "Childhood Acute Monocytic Leukemia with Differentiation", "Childhood Acute Differentiated Monocytic Leukemia (M5b)", "childhood acute monocytic leukemia with differentiation", "pediatric acute monocytic leukemia with differentiation", "Pediatric Acute Monocytic Leukemia with Differentiation", "leukemia, childhood acute monocytic with differentiation", "monocytic leukemia with differentiation, childhood acute", "acute monocytic leukemia with differentiation, childhood", "M5b pediatric acute monocytic leukemia with differentiation", "M5b childhood acute monocytic leukemia with differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Acute Monocytic Leukemia", "shortest_name_length": 24}
{"curie": "MONDO:0018493", "names": ["MH", "malignant fever", "Fever malignant", "FEVER MALIGNANT", "malignant hyperthemia", "MALIGNANT HYPERTHEMIA", "Hyperthermia malignant", "Malignant Hyperpyrexia", "hyperpyrexia malignant", "Hyperpyrexia malignant", "malignant hyperpyrexia", "HYPERPYREXIA MALIGNANT", "Malignant Hyperthermia", "Malignant hyperpyrexia", "MALIGNANT HYPERTHERMIA", "Malignant hyperthermia", "malignant hyperthermia", "hyperthermia malignant", "HYPERTHERMIA MALIGNANT", "malignant; hyperthermia", "Hyperpyrexia, Malignant", "hyperpyrexia; malignant", "HYPERPYREXIA, MALIGNANT", "HYPERTHERMIA, MALIGNANT", "Anesthesia Hyperthermia", "Malignant Hyperpyrexias", "malignant; hyperpyrexia", "hyperthermia; malignant", "Hyperthermia, Malignant", "HYPERPYREXIA, FULMINATING", "Hyperthermia of anesthesia", "hyperthermia of anesthesia", "Hyperthermia of Anesthesia", "HYPERTHERMIA OF ANESTHESIA", "MH - Malignant hyperpyrexia", "Hyperthermia of anaesthesia", "MHS - Malignant hyperthermia", "anesthesia related hyperthermia", "malignant hyperthermia syndrome", "Anesthesia Related Hyperthermia", "Malignant Hyperthermia Syndrome", "Hyperthermia, Anesthesia Related", "Malignant hyperthermia (finding)", "malignant hyperthermia (diagnosis)", "malignant hyperthermia of anesthesia", "Malignant hyperthermia of anesthesia", "Malignant hyperthermia with anesthesia", "Malignant hyperthermia with anaesthesia", "Malignant hyperthermia due to anesthesia", "Malignant hyperpyrexia due to anesthesia", "Malignant hyperpyrexia due to anesthetic", "malignant hyperthermia due to anesthesia", "malignant hyperpyrexia due to anesthesia", "Malignant hyperthermia due to anaesthesia", "Malignant hyperpyrexia due to anaesthetic", "Malignant hyperpyrexia due to anaesthesia", "Malignant hyperpyrexia caused by anesthetic", "Malignant hyperpyrexia caused by anesthesia", "Malignant hyperthermia caused by anesthesia", "Malignant hyperpyrexia caused by anaesthetic", "Malignant hyperpyrexia caused by anaesthesia", "Malignant hyperthermia caused by anaesthesia", "anesthesia; complication, malignant hyperthermia", "anesthesia; complication, hyperthermia, malignant", "complications; anesthesia, malignant hyperthermia", "complications; anesthesia, hyperthermia, malignant", "malignant hyperthermia due to anesthesia (diagnosis)", "Malignant hyperpyrexia caused by anesthetic (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant hyperthermia of anesthesia", "shortest_name_length": 2}
{"curie": "UMLS:C3502073", "names": ["Woolly Hair, Autosomal Recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Woolly Hair, Autosomal Recessive", "shortest_name_length": 32}
{"curie": "MONDO:0004422", "names": ["falx meningioma", "Falx meningioma", "meningioma (falx)", "Falcine Meningioma", "Falcine meningioma", "falx cerebri meningioma", "Falx Cerebri Meningioma", "Cerebral Falx Meningioma", "cerebral falx meningioma", "meningioma of falx cerebri", "Meningioma of Falx Cerebri", "Meningioma of Cerebral Falx", "meningioma of cerebral falx", "meningioma of the falx cerebri", "Meningioma of Falx of Cerebrum", "meningioma of falx of cerebrum", "Meningioma of the Falx Cerebri", "meningioma of the cerebral falx", "Meningioma of the Cerebral Falx", "falx cerebri meningioma (disease)", "meningioma (disease) of falx cerebri", "Meningioma of the Falx of the Cerebrum", "meningioma of the falx of the cerebrum", "meningioma of falx cerebri (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral falx meningioma", "shortest_name_length": 15}
{"curie": "UMLS:C4553247", "names": ["Stage II Urethral Cancer", "Stage II Urethral Cancer AJCC v8", "Stage II Urethral Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Urethral Cancer AJCC v8", "shortest_name_length": 24}
{"curie": "MONDO:0012205", "names": ["ADSD", "ADSD1", "striatal degeneration, autosomal dominant", "STRIATAL DEGENERATION, AUTOSOMAL DOMINANT 1", "striatal Degeneration, autosomal dominant 1", "striatal degeneration, autosomal dominant 1", "autosomal dominant striatal neurodegeneration", "Autosomal dominant striatal neurodegeneration", "PDE8B striatal degeneration, autosomal dominant", "autosomal dominant striatal neurodegeneration type 1", "ADSD - autosomal dominant striatal neurodegeneration", "Autosomal dominant striatal neurodegeneration (disorder)", "striatal degeneration, autosomal dominant caused by mutation in PDE8B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant striatal neurodegeneration type 1", "shortest_name_length": 4}
{"curie": "MONDO:0010658", "names": ["MRXS12", "Mental Retardation, X-Linked, Syndromic 12", "mental retardation, X-linked, syndromic 12", "MENTAL RETARDATION, X-LINKED, SYNDROMIC 12", "X-linked intellectual disability Wilson type", "syndromic X-linked intellectual disability 12", "X-linked intellectual disability, Wilson type", "intellectual disability, X-linked, syndromic 12", "syndromic X-linked intellectual disability type 12", "X-linked intellectual disability Wilson type (disorder)", "X-linked intellectual disability Wilson type (diagnosis)", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic X-linked intellectual disability 12", "shortest_name_length": 6}
{"curie": "MONDO:0005674", "names": ["GCT of bone", "OSTEOCLASTOMA", "Osteoclastoma", "osteoclastoma", "osteoclastomas", "giant cell myeloma", "Osteoclastoma, NOS", "giant cell tumor bone", "giant cell bone tumor", "Osteoclastoma, benign", "bone giant cell tumor", "Osteoclastoma, Benign", "Bone giant cell tumor", "bone cell giant tumor", "bone giant cell tumour", "BONE, GIANT CELL TUMOR", "Bone giant cell tumour", "giant cell; tumor, bone", "bone cell giant tumours", "tumor; giant cell, bone", "Giant cell tumor of bone", "GIANT CELL TUMOR OF BONE", "giant cell tumor of bone", "Giant Cell Tumor of Bone", "giant cell tumor, benign", "GIANT CELL TUMOR, BENIGN", "Giant cell tumour of bone", "giant cell neoplasm of bone", "Giant cell neoplasm of bone", "Giant cell tumor of bone NOS", "giant cell tumor of the bone", "benign bone giant cell tumor", "Benign Bone Giant Cell Tumor", "Bone giant cell tumor benign", "Benign bone giant cell tumor", "Giant Cell Tumor of the Bone", "Bone giant cell tumour benign", "Giant cell tumour of bone NOS", "Benign bone giant cell tumour", "Giant cell tumor of bone, NOS", "Giant cell tumour of bone, NOS", "benign giant cell tumor of bone", "GTCT - Giant cell tumor of bone", "benign giant-cell tumor in bone", "Giant cell tumor of bone (disorder)", "giant cell tumor of bone (diagnosis)", "benign giant-cell tumor in bone (diagnosis)", "Giant cell tumor of bone (morphologic abnormality)", "giant cell tumor of bone (morphologic abnormality)", "giant cell tumor of bone NOS (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bone giant cell tumor", "shortest_name_length": 11}
{"curie": "UMLS:C0279579", "names": ["Anaplastic Adrenal Cortex Cancer", "anaplastic adrenocortical cancer", "adrenal cortex cancer, anaplastic", "Anaplastic Adrenal Cortex Carcinoma", "anaplastic adrenocortical carcinoma", "Anaplastic adrenocortical carcinoma", "Adrenal Cortex Anaplastic Carcinoma", "carcinoma, anaplastic adrenocortical", "adrenocortical carcinoma, anaplastic", "Adrenal Cortex Sarcomatoid Carcinoma", "carcinoma, adrenocortical, anaplastic", "adrenal cortical, anaplastic carcinoma", "adrenal cortical carcinoma, anaplastic", "Adrenal Cortical Sarcomatoid Carcinoma", "undifferentiated adrenocortical carcinoma", "carcinoma, undifferentiated adrenocortical"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anaplastic adrenocortical carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0025087", "names": ["Swine Fever", "Hog cholera", "swine fever", "hog cholera", "Hog Cholera", "cholera, Hog", "Cholera, Hog", "Classical swine fever", "classical swine fever", "Classical Swine Fever", "swine fever, classical", "Swine Fever, Classical", "Hog cholera (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "classical swine fever", "shortest_name_length": 11}
{"curie": "UMLS:C1963737", "names": ["Radiation necrosis", "radiation necrosis", "Radiation Necrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radiation necrosis", "shortest_name_length": 18}
{"curie": "MONDO:0000214", "names": ["hypermanganesemia with dystonia", "Hypermanganesemia with dystonia", "Familial manganese-induced neurotoxicity", "HMNDYT - hypermanganesemia with dystonia", "Hypermanganesemia with dystonia (disorder)", "Hypermanganesemia with dystonia (diagnosis)", "disorders of manganese metabolism hypermanganesemia with dystonia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypermanganesemia with dystonia", "shortest_name_length": 31}
{"curie": "MONDO:0012557", "names": ["Mpcd", "MPCD", "Mitochondrial Phosphate Carrier Deficiency", "MITOCHONDRIAL PHOSPHATE CARRIER DEFICIENCY", "mitochondrial phosphate carrier deficiency", "Mitochondrial phosphate carrier deficiency", "cardiomyopathy-hypotonia-lactic acidosis syndrome", "Mitochondrial phosphate carrier deficiency (disorder)", "Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome", "hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome", "Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder)", "NEONATAL HYPERTROPHIC CARDIOMYOPATHY, RESPIRATORY INSUFFICIENCY, HYPOTONIA, AND LACTIC ACIDOSIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiomyopathy-hypotonia-lactic acidosis syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0016673", "names": ["JEB-nH loc", "localized junctional epidermolysis bullosa, non-Herlitz type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "localized junctional epidermolysis bullosa, non-Herlitz type", "shortest_name_length": 10}
{"curie": "MONDO:0100465", "names": ["complex neurodevelopmental disorder with or without congenital anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complex neurodevelopmental disorder with or without congenital anomalies", "shortest_name_length": 72}
{"curie": "MONDO:0012362", "names": ["CMD1P", "Dilated Cardiomyopathy-1P", "dilated cardiomyopathy 1P", "CARDIOMYOPATHY, DILATED, 1P", "Cardiomyopathy, Dilated, 1p", "cardiomyopathy, dilated, 1P", "dilated cardiomyopathy type 1P", "cardiomyopathy, dilated, type 1P", "PLN familial isolated dilated cardiomyopathy", "familial isolated dilated cardiomyopathy caused by mutation in PLN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1P", "shortest_name_length": 5}
{"curie": "MONDO:0001886", "names": ["Midline cystocele", "midline cystocele", "Cystocele, midline", "Midline cystocele (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "midline cystocele", "shortest_name_length": 17}
{"curie": "UMLS:C1565885", "names": ["Neonatal Direct Hyperbilirubinemia", "Direct Hyperbilirubinemia, Neonatal", "Hyperbilirubinemia, Neonatal Direct"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Direct Hyperbilirubinemia, Neonatal", "shortest_name_length": 34}
{"curie": "UMLS:C5394779", "names": ["Malignant melanoma with BRAF V600E mutation", "Malignant melanoma with B-Raf proto-oncogene, serine/threonine kinase V600E mutation", "Malignant melanoma with B-Raf proto-oncogene, serine/threonine kinase V600E mutation (disorder)", "Malignant melanoma with B-Raf proto-oncogene, serine/threonine kinase V600E mutation (diagnosis)", "Malignant melanoma with B-Raf proto-oncogene, serine/threonine kinase V600E mutation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant melanoma with BRAF V600E mutation", "shortest_name_length": 43}
{"curie": "MONDO:0012589", "names": ["PTHS", "Pitt Hopkins syndrome", "Pitt-Hopkins syndrome", "PITT-HOPKINS SYNDROME", "Pitt-Hopkins Syndrome", "PTHS - Pitt-Hopkins syndrome", "Pitt-Hopkins syndrome (disorder)", "Pitt-Hopkins syndrome (diagnosis)", "encephalopathy, Severe epileptic, with autonomic dysfunction", "Encephalopathy, Severe Epileptic, With Autonomic Dysfunction", "ENCEPHALOPATHY, SEVERE EPILEPTIC, WITH AUTONOMIC DYSFUNCTION", "MENTAL RETARDATION, SYNDROMAL, WITH INTERMITTENT HYPERVENTILATION", "Mental Retardation, Syndromal, With Intermittent Hyperventilation", "mental retardation, Syndromal, with intermittent hyperventilation", "intellectual disability, Syndromal, with intermittent hyperventilation", "intellectual disability, wide mouth, distinctive facial features, and intermittent hyperventilation followed by apnea"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pitt-Hopkins syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0854211", "names": ["Bacterial keratitis", "Keratitis bacterial", "bacterial keratitis", "Keratitis bacterial NOS", "Bacterial keratitis (disorder)", "Bacterial keratoconjunctivitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bacterial keratitis", "shortest_name_length": 19}
{"curie": "UMLS:C0234298", "names": ["Primary sweet taste disorder", "Taste Disorder, Primary, Sweet", "Taste disorder, primary, sweet", "Primary sweet taste disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Taste Disorder, Primary, Sweet", "shortest_name_length": 28}
{"curie": "MONDO:0001576", "names": ["hyphenwebs", "Hyphenwebs", "Spider vein", "Spider Vein", "spider vein", "vein spider", "thread vein", "Spider Veins", "spider veins", "Spider veins", "Thread veins", "thread veins", "Vein, Spider", "Spider-burst", "Veins, Spider", "Veins, spider", "telangiectasis", "TELANGIECTASIS", "Telangiectases", "Telangiectasia", "TELANGIECTASIA", "telangiectases", "Telangiectasis", "TELANGIECTASES", "telangiectasia", "TELANGIECTASIAS", "Telangiectasias", "telangiectasias", "Telangiectasis, NOS", "Telangiectasia, NOS", "Telangiectasia disorder", "spider vein (diagnosis)", "Cutaneous telangiectasia", "telangiectasia (physical finding)", "Telangiectasia disorder (disorder)", "Telangiectasia disorder (diagnosis)", "Telangiectasis (morphologic abnormality)", "peripheral vascular disease telangiectasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "telangiectasis", "shortest_name_length": 10}
{"curie": "UMLS:C0751402", "names": ["OPTIC DISC DISEASE", "optic disc disease", "Optic disk disorder", "optic disc disorder", "Optic Disk Disorder", "Optic Disc Disorder", "Optic disc disorder", "disc diseases optic", "optic disc disorders", "Disk Disorder, Optic", "Disc Disorder, Optic", "Optic Disc Disorders", "Disorder, Optic Disc", "Optic Disk Disorders", "Disorder of optic disc", "Optic disc disorder NOS", "Optic disc disorder (disorder)", "optic disc disorders (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Optic Disk Disorders", "shortest_name_length": 18}
{"curie": "MONDO:0044720", "names": ["CANVAS", "CABV syndrome", "cerebellar ataxia with bilateral vestibulopathy syndrome", "Cerebellar ataxia with bilateral vestibulopathy syndrome", "CABV (cerebellar ataxia, bilateral vestibulopathy) syndrome", "CEREBELLAR ATAXIA, NEUROPATHY, AND VESTIBULAR AREFLEXIA SYNDROME", "cerebellar ataxia, neuropathy, and vestibular areflexia syndrome", "CANVAS - cerebellar ataxia, neuropathy, vestibular areflexia syndrome", "cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome", "Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome", "Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0012739", "names": ["Balikova-Vermeesch syndrome", "MICROTIA WITH NASOLACRIMAL DUCT IMPERFORATION AND EYE COLOBOMA", "Microtia With Nasolacrimal Duct Imperforation And Eye Coloboma", "microtia with nasolacrimal duct imperforation and eye coloboma", "microtia eye coloboma and imperforation of the nasolacrimal duct", "microtia-eye coloboma-imperforation of the nasolacrimal duct syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microtia-eye coloboma-imperforation of the nasolacrimal duct syndrome", "shortest_name_length": 27}
{"curie": "MONDO:0003128", "names": ["classic pulmonary blastoma", "Classic Pulmonary Blastoma", "biphasic pulmonary blastoma", "Biphasic Pulmonary Blastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "classic pulmonary blastoma", "shortest_name_length": 26}
{"curie": "MONDO:0009420", "names": ["Al Awadi Farag Teebi syndrome", "Al Awadi Teebi Farag syndrome", "Al Awadi-Farag-Teebi syndrome", "Teebi Naguib Al Awadi syndrome", "Hypergonadotropic Hypogonadism And Partial Alopecia", "HYPERGONADOTROPIC HYPOGONADISM AND PARTIAL ALOPECIA", "hypergonadotropic hypogonadism and partial alopecia", "Primary hypergonadotropic hypogonadism-partial alopecia syndrome", "primary hypergonadotropic hypogonadism-partial alopecia syndrome", "Primary hypergonadotropic hypogonadism and partial alopecia syndrome", "Primary hypergonadotropic hypogonadism and partial alopecia syndrome (disorder)", "Profound limb deficiency, thoracic dystrophy, unusual facies, and normal intelligence"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary hypergonadotropic hypogonadism-partial alopecia syndrome", "shortest_name_length": 29}
{"curie": "MONDO:0007819", "names": ["SMMCI", "SMMCI SYNDROME", "SMMCI Syndrome", "SMMCI syndrome", "FUSED INCISORS", "Fused incisors", "incisors fused", "Incisors, Fused", "INCISORS, FUSED", "incisors, Fused", "Single median incisor", "Single central incisor", "Only one upper front tooth", "Single upper central incisor", "single upper central incisor", "Single central upper incisor", "SINGLE UPPER CENTRAL INCISOR", "Single median maxillary incisor", "Single midline upper front tooth", "Single maxillary central incisor", "Single midline maxillary incisor", "SINGLE CENTRAL MAXILLARY INCISOR", "single central maxillary incisor", "Single central maxillary incisor", "single median maxillary central incisor", "Solitary median maxillary central incisor", "solitary MEDIAN maxillary central incisor", "SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR", "Solitary midline maxillary central incisor", "SMMCI Solitary median maxillary central incisor", "solitary median maxillary central incisor syndrome", "Solitary median maxillary central incisor syndrome", "SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR SYNDROME", "Solitary median maxillary central incisor syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "solitary median maxillary central incisor syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C4330675", "names": ["Metastatic Prostate Cancer in the Soft Tissue", "Metastatic Prostate Carcinoma in the Soft Tissue", "Prostate Carcinoma Metastatic in the Soft Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Carcinoma Metastatic in the Soft Tissue", "shortest_name_length": 45}
{"curie": "MONDO:0001992", "names": ["Rete Testis Adenocarcinoma", "rete testis adenocarcinoma", "adenocarcinoma of rete testis", "Adenocarcinoma of Rete Testis", "adenocarcinoma of the rete testis", "carcinoma, rete testis, malignant", "Adenocarcinoma of the rete testis", "CARCINOMA, RETE TESTIS, MALIGNANT", "Adenocarcinoma of the Rete Testis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rete testis adenocarcinoma", "shortest_name_length": 26}
{"curie": "UMLS:C4727586", "names": ["Recurrent Peripheral T-Cell Lymphoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Peripheral T-Cell Lymphoma, Not Otherwise Specified", "shortest_name_length": 61}
{"curie": "UMLS:C1334936", "names": ["Tumor of Uncertain Origin", "Neoplasm of Uncertain Origin", "Tumor of Uncertain Histogenesis", "Neoplasm of Uncertain Histogenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplasm of Uncertain Histogenesis", "shortest_name_length": 25}
{"curie": "MONDO:0017191", "names": ["sporadic pheochromocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sporadic pheochromocytoma", "shortest_name_length": 25}
{"curie": "UMLS:C5204071", "names": ["Locally Advanced Prostate Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Prostate Neuroendocrine Carcinoma", "shortest_name_length": 50}
{"curie": "MONDO:0012666", "names": ["ASRT6", "asthma-related traits, susceptibility to, 6", "ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 6", "asthma-related traits, susceptibility to, type 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "asthma-related traits, susceptibility to, 6", "shortest_name_length": 5}
{"curie": "UMLS:C5419809", "names": ["Small pHCC", "Small Progressed Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Progressed Hepatocellular Carcinoma", "shortest_name_length": 10}
{"curie": "MONDO:0013456", "names": ["DHFR DEFICIENCY", "DHFR Deficiency", "DHFR deficiency", "dihydrofolate reductase deficiency", "Dihydrofolate reductase deficiency", "Deficiency of dihydrofolate reductase", "Deficiency of tetrahydrofolate dehydrogenase", "dihydrofolate reductase deficiency (diagnosis)", "Deficiency of dihydrofolate reductase (disorder)", "Megaloblastic Anemia due to Dihydrofolate Reductase Deficiency", "Megaloblastic anemia due to dihydrofolate reductase deficiency", "megaloblastic anemia due to dihydrofolate reductase deficiency", "MEGALOBLASTIC ANEMIA DUE TO DIHYDROFOLATE REDUCTASE DEFICIENCY", "Megaloblastic anaemia due to dihydrofolate reductase deficiency", "Constitutional megaloblastic anemia with severe neurologic disease", "constitutional megaloblastic anemia with severe neurologic disease", "Megaloblastic anemia due to dihydrofolate reductase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "constitutional megaloblastic anemia with severe neurologic disease", "shortest_name_length": 15}
{"curie": "MONDO:0700131", "names": ["sarcoma, non-human animal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sarcoma, non-human animal", "shortest_name_length": 25}
{"curie": "UMLS:C1541844", "names": ["Presenile And Senile Dementia", "PRESENILE AND SENILE DEMENTIA", "Presenile and senile dementia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PRESENILE AND SENILE DEMENTIA", "shortest_name_length": 29}
{"curie": "MONDO:0011650", "names": ["AVSD2", "CRELD1 atrioventricular septal defect", "susceptibility to atrioventricular septal defect 2", "atrioventricular septal defect, susceptibility to, 2", "ATRIOVENTRICULAR SEPTAL DEFECT, SUSCEPTIBILITY TO, 2", "atrioventricular septal defect, susceptibility to, type 2", "atrioventricular septal defect caused by mutation in CRELD1", "ATRIOVENTRICULAR SEPTAL DEFECT, PARTIAL, WITH HETEROTAXY SYNDROME", "Atrioventricular Septal Defect, Partial, with Heterotaxy Syndrome", "atrioventricular septal defect, partial, with heterotaxy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrioventricular septal defect, susceptibility to, 2", "shortest_name_length": 5}
{"curie": "MONDO:0032603", "names": ["PAPA9", "POLYDACTYLY, POSTAXIAL, TYPE A9", "polydactyly, postaxial, type A9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polydactyly, postaxial, type A9", "shortest_name_length": 5}
{"curie": "MONDO:0011318", "names": ["TONOKI SYNDROME", "Tonoki syndrome", "short stature, brachydactyly, nail dysplasia and mental retardation", "Short stature, brachydactyly, nail dysplasia, and mental retardation", "short stature, brachydactyly, nail dysplasia and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tonoki syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0017515", "names": ["short fingers, unilateral", "brachydactyly of fingers, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly of fingers, unilateral", "shortest_name_length": 25}
{"curie": "UMLS:C1841973", "names": ["Pseudohermaphroditism, Female, With Hypokalemia, Due To Glucocorticoid Resistance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pseudohermaphroditism, Female, With Hypokalemia, Due To Glucocorticoid Resistance", "shortest_name_length": 81}
{"curie": "UMLS:C2204358", "names": ["Salivary Gland Follicular Lymphoma", "follicular lymphoma of salivary gland", "Primary Salivary Gland Follicular Lymphoma", "follicular lymphoma of salivary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "follicular lymphoma of salivary gland", "shortest_name_length": 34}
{"curie": "UMLS:C5204613", "names": ["Bladder Angiosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder Angiosarcoma", "shortest_name_length": 20}
{"curie": "MONDO:0043101", "names": ["Hypothalamic syndrome", "hypothalamic syndrome", "dysfunction hypothalamic", "Hypothalamic dysfunction", "hypothalamic dysfunction", "dysfunction; hypothalamic", "Hypothalamic syndrome, NOS", "Hypothalamic syndrome (disorder)", "Hypothalamic Dysfunction Syndrome", "Hypothalamic Dysfunction Syndromes", "Syndrome, Hypothalamic Dysfunction", "Dysfunction Syndrome, Hypothalamic", "Syndromes, Hypothalamic Dysfunction", "Dysfunction Syndromes, Hypothalamic", "hypothalamic dysfunction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypothalamic dysfunction", "shortest_name_length": 21}
{"curie": "MONDO:0017692", "names": ["generalized GALE-D", "Generalized GALE-D", "Generalized GALE deficiency", "generalized GALE deficiency", "Generalized galactose epimerase deficiency", "generalized galactose epimerase deficiency", "Generalized epimerase deficiency galactosemia", "generalized epimerase deficiency galactosemia", "Generalized UDP-galactose-4-epimerase deficiency", "generalized UDP-galactose-4-epimerase deficiency", "Generalised uridine diphosphate galactose-4-epimerase deficiency", "Generalized uridine diphosphate galactose-4-epimerase deficiency", "generalized uridine diphosphate galactose-4-epimerase deficiency", "Generalized uridine diphosphate galactose-4-epimerase deficiency (disorder)", "Generalized uridine diphosphate galactose-4-epimerase deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "generalized galactose epimerase deficiency", "shortest_name_length": 18}
{"curie": "UMLS:C4520993", "names": ["Stage I Liver Cell Cancer", "Liver Cell Cancer Stage I", "Stage I Liver Cell Carcinoma", "Stage I Hepatocellular Cancer", "Hepatocellular Cancer Stage I", "Stage I Hepatocellular Carcinoma AJCC v6", "Stage I Hepatocellular Carcinoma AJCC v7", "Stage I Hepatocellular Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Hepatocellular Carcinoma AJCC v6 and v7", "shortest_name_length": 25}
{"curie": "MONDO:0006598", "names": ["phototoxicity", "Phototoxicity", "Photodermatitis", "Photosensitized", "photosensitizing", "Phototoxic eczema", "Photosensitiveness", "photosensitiveness", "Photosensitive rash", "phototoxic reaction", "Phototoxic reaction", "phototoxic reactions", "photosensitivity rash", "Phototoxic dermatitis", "phototoxic dermatitis", "RASH PHOTOSENSITIVITY", "Phototoxic Dermatitis", "Rash photosensitivity", "Dermatitis, Phototoxic", "Phototoxicity (finding)", "Phototoxic Dermatitides", "Photosensitive reaction", "Dermatitides, Phototoxic", "Photosensitivity Reaction", "Photosensitive Dermatitis", "photosensitive dermatitis", "PHOTOSENSITIVITY REACTION", "photosensitivity reaction", "Photosensitive dermatitis", "Dermatitis photosensitive", "Photosensitivity reaction", "Phototoxic dermatitis, NOS", "photosensitivity reactions", "Photosensitization reaction", "Photosensitisation reaction", "Phototoxic Contact Dermatitis", "phototoxic contact dermatitis", "Photosensitivity reaction NOS", "Dermatitis, Phototoxic Contact", "Contact Dermatitis, Phototoxic", "Phototoxic Contact Dermatitides", "PHOTOSENSITIVITY REACTION (NOS)", "REACTION PHOTOSENSITIVITY (NOS)", "PHOTOSENSITIVITY TOXIC REACTION", "Dermatitis, Contact, Phototoxic", "Photosensitivity toxic reaction", "Phototoxic dermatitis (disorder)", "Dermatitides, Phototoxic Contact", "Contact Dermatitides, Phototoxic", "phototoxic contact dermatitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phototoxic dermatitis", "shortest_name_length": 13}
{"curie": "UMLS:C1261281", "names": ["Renal transplant disorder", "Kidney transplant disorder", "complication kidney transplant", "Disorder of transplanted kidney", "complications kidney transplant", "complications; kidney transplant", "kidney transplant; complications", "Transplanted Kidney Complication", "complication of renal transplant", "Complications of kidney transplant", "Complication of Transplanted Kidney", "complication of transplanted kidney", "Complication of transplanted kidney", "Complications of transplanted kidney", "complication of renal transplant (diagnosis)", "Complication of transplanted kidney (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disorder of transplanted kidney", "shortest_name_length": 25}
{"curie": "MONDO:0000716", "names": ["Agraphia", "AGRAPHIA", "agraphia", "Agraphias", "dysgraphia", "Dysgraphia", "Dysgraphias", "Agraphia NOS", "Agraphia (finding)", "Dysgraphia (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "agraphia", "shortest_name_length": 8}
{"curie": "UMLS:C5419818", "names": ["Gallbladder Adenoma, Intestinal-Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gallbladder Adenoma, Intestinal-Type", "shortest_name_length": 36}
{"curie": "UMLS:C3814879", "names": ["Phosphaturic mesenchymal tumor", "Phosphaturic mesenchymal tumour", "Benign Phosphaturic Mesenchymal Tumor", "Phosphaturic mesenchymal tumor, benign", "Phosphaturic mesenchymal tumour, benign", "Phosphaturic mesenchymal tumor, benign (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Phosphaturic mesenchymal tumor, benign", "shortest_name_length": 30}
{"curie": "MONDO:0030868", "names": ["SPGF98", "SPGF49", "SPERMATOGENIC FAILURE 49", "spermatogenic failure 49"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 49", "shortest_name_length": 6}
{"curie": "MONDO:0018852", "names": ["ACHM", "Achromatism", "achromatism", "achromatopsia", "Achromatopsia", "monochromatism", "Achromatopsias", "Monochromatism", "Achromatopsia 1", "Rod monochromacy", "Rod monochromatism", "Pingelapese blindness", "total color blindness", "Total color blindness", "Blindness colour total", "Complete color blindness", "Achromatopsia (disorder)", "achromatopsia (diagnosis)", "achromatopsia (physical finding)", "complete or incomplete color blindness", "Complete or incomplete color blindness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "achromatopsia", "shortest_name_length": 4}
{"curie": "MONDO:0003095", "names": ["larynx mucoepidermoid carcinoma", "mucoepidermoid carcinoma of larynx", "Mucoepidermoid carcinoma of Larynx", "laryngeal mucoepidermoid carcinoma", "Laryngeal Mucoepidermoid Carcinoma", "Mucoepidermoid Carcinoma of Larynx", "mucoepidermoid carcinoma of the larynx", "laryngeal throat mucoepidermoid cancer", "Laryngeal Throat Mucoepidermoid Cancer", "Mucoepidermoid Carcinoma of the Larynx", "mucoepidermoid carcinoma of larynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laryngeal mucoepidermoid carcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C0021508", "names": ["disorder of environmental origin", "Disorders of Environmental Origin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disorders of Environmental Origin", "shortest_name_length": 32}
{"curie": "MONDO:0016301", "names": ["L-transposition", "Double discordance", "ventricle; inversion", "ventricular inversion", "Ventricular inversion", "ventricular; inversion", "inversion; ventricular", "Congenitally Corrected TGA", "TGA, Congenitally Corrected", "Congenitally Corrected TGAs", "L-transposition of the great vessels", "L-Transposition of the Great Vessels", "Congenitally Corrected Transposition", "Congenitally Corrected Transpositions", "L-transposition of the great arteries", "Transposition, Congenitally Corrected", "Levo-Transposition of the Great Vessels", "levo-transposition of the great vessels", "Levo-Transposition of the Great Arteries", "Levo-transposition of the great arteries", "levo-transposition of the great arteries", "Corrected transposition of great vessels", "Ventriculoarterial and atrioventricular discordance", "Corrected transposition of great vessels (disorder)", "ventriculoarterial and atrioventricular discordance", "Congenitally corrected transposition of great arteries", "congenitally corrected transposition of the great vessels", "Transposition of great vessels with ventricular inversion", "Congenitally Corrected Transposition of the Great Vessels", "Congenitally corrected transposition of the great vessels", "congenitally corrected transposition of the great arteries", "Congenitally corrected transposition of the great arteries", "transposition of the great vessels, congenitally corrected", "Congenitally Corrected Transposition of the Great Arteries", "transposition of the great arteries, congenitally corrected", "Discordant ventriculoarterial and atrioventricular connections", "discordant ventriculoarterial and atrioventricular connections", "[OBSOLETE] Congenitally corrected transposition of the great arteries", "Discordant ventriculoarterial connection with discordant atrioventricular connection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenitally corrected transposition of the great arteries", "shortest_name_length": 15}
{"curie": "MONDO:0003464", "names": ["cystadenofibroma", "Cystadenofibroma", "Cystadenofibromas", "cystadenofibromas", "Cystadenofibroma, NOS", "Clear cell adenofibroma", "Clear Cell Adenofibroma", "Clear Cell Adenofibromas", "Adenofibroma, Clear Cell", "Adenofibromas, Clear Cell", "cystadenofibroma; unspecified site", "Clear cell adenofibroma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cystadenofibroma", "shortest_name_length": 16}
{"curie": "UMLS:C0860634", "names": ["pseudocoma", "Pseudocoma", "pseudocomas", "Pseudocomas", "psychogenic coma", "Psychogenic coma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Psychogenic coma", "shortest_name_length": 10}
{"curie": "MONDO:0014609", "names": ["CHOPS", "CHOPS syndrome", "CHOPS SYNDROME", "Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome", "COGNITIVE IMPAIRMENT, COARSE FACIES, HEART DEFECTS, OBESITY, PULMONARY INVOLVEMENT, SHORT STATURE, AND SKELETAL DYSPLASIA", "cognitive impairment, coarse facies, heart defects, obesity, pulmonary involvement, short stature, and skeletal dysplasia", "Cognitive impairment, coarse facies, heart defects, obesity, pulmonary involvement, short stature, skeletal dysplasia syndrome", "cognitive impairment, coarse facies, heart defects, obesity, pulmonary involvement, short stature, skeletal dysplasia syndrome", "cognitive impairment - coarse facies - heart defects - obesity - pulmonary involvement - short stature - skeletal dysplasia syndrome", "Cognitive impairment, coarse facies, heart defects, obesity, pulmonary involvement, short stature, skeletal dysplasia syndrome (disorder)", "cognitive impairment, coarse facies, heart defects, obesity, pulmonary involvement, short stature, skeletal dysplasia syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cognitive impairment - coarse facies - heart defects - obesity - pulmonary involvement - short stature - skeletal dysplasia syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0002056", "names": ["FA", "fibroadenoma", "Breast mouse", "Fibroadenoma", "breast mouse", "fibroadenomas", "Fibroadenomas", "Fibroadenoma NOS", "Fibroadenoma, NOS", "Benign fibroadenoma", "breast fibroadenoma", "Breast Fibroadenoma", "fibroadenoma breast", "Breast fibroadenoma", "adenofibroma breast", "fibroadenoma, benign", "FIBROADENOMA, BENIGN", "Breast fibroadenosis", "BREAST, ADENOFIBROMA", "Breast fibroadenomas", "BREAST, FIBROADENOMA", "Complex Fibroadenoma", "breast fibroadenomas", "cellular fibroadenoma", "cellular Fibroadenoma", "juvenile fibroadenoma", "Juvenile fibroadenoma", "Juvenile Fibroadenoma", "Cellular fibroadenoma", "fibroadenoma; juvenile", "FIBROADENOMA OF BREAST", "Fibroadenoma of Breast", "fibroadenoma of breast", "Fibroadenoma of breast", "juvenile; fibroadenoma", "Fibroadenosis - breast", "Fibroadenosis of breast", "Fibroadenoma of the Breast", "Fibroadenoma of the breast", "fibroadenoma of the breast", "Breast Complex Fibroadenoma", "Complex Breast Fibroadenoma", "Breast Juvenile Fibroadenoma", "Juvenile Breast Fibroadenoma", "Complex fibroadenoma of breast", "fibroadenoma; unspecified site", "Complex Fibroadenoma of breast", "Complex Fibroadenoma of Breast", "Juvenile Fibroadenoma of Breast", "juvenile fibroadenoma of breast", "Juvenile fibroadenoma of breast", "Fibroadenoma of breast (disorder)", "fibroadenoma of breast (diagnosis)", "Complex Fibroadenoma of the Breast", "Juvenile Fibroadenoma of the Breast", "Juvenile fibroadenoma of breast (disorder)", "Benign fibroadenoma (morphologic abnormality)", "juvenile fibroadenoma (morphologic abnormality)", "Juvenile fibroadenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast fibroadenoma", "shortest_name_length": 2}
{"curie": "MONDO:0021313", "names": ["eyelid cancer", "cancer of eyelid", "Malignant Eyelid Tumor", "malignant eyelid tumor", "malignant eyelid neoplasm", "Malignant Tumor of Eyelid", "Malignant Eyelid Neoplasm", "malignant tumor of eyelid", "malignant neoplasm of eyelid", "Malignant Neoplasm of Eyelid", "malignant tumor of the eyelid", "Malignant Tumor of the Eyelid", "Malignant Neoplasm of the Eyelid", "malignant neoplasm of the eyelid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eyelid cancer", "shortest_name_length": 13}
{"curie": "MONDO:0043969", "names": ["sleep related dystonia", "Sleep-related dystonia", "sleep-related dystonia", "Sleep-Related Dystonia", "Sleep Related Dystonia", "Dystonia, Sleep-Related", "Sleep-Related Dystonias", "dystonia, sleep-related", "sleep-related dystonias", "dystonias, sleep-related", "Dystonias, Sleep-Related", "nocturnal paroxysmal dystonia", "paroxysmal nocturnal dystonia", "Nocturnal Paroxysmal Dystonia", "dystonia, nocturnal paroxysmal", "Nocturnal Paroxysmal Dystonias", "nocturnal paroxysmal dystonias", "Paroxysmal Dystonia, Nocturnal", "paroxysmal dystonia, nocturnal", "hypnogenic paroxysmal dystonia", "Dystonia, Nocturnal Paroxysmal", "Hypnogenic Paroxysmal Dystonia", "paroxysmal dystonia, hypnogenic", "dystonia, nocturnal, paroxysmal", "Dystonias, Nocturnal Paroxysmal", "dystonias, nocturnal paroxysmal", "Paroxysmal Dystonias, Nocturnal", "paroxysmal dystonias, nocturnal", "Paroxysmal Dystonia, Hypnogenic", "hypnogenic paroxysmal dystonias", "dystonia, hypnogenic paroxysmal", "Dystonia, Nocturnal, Paroxysmal", "Dystonia, Hypnogenic Paroxysmal", "Hypnogenic Paroxysmal Dystonias", "Dystonias, Hypnogenic Paroxysmal", "paroxysmal dystonias, hypnogenic", "dystonias, hypnogenic paroxysmal", "Paroxysmal Dystonias, Hypnogenic", "Sleep-related dystonia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nocturnal paroxysmal dystonia", "shortest_name_length": 22}
{"curie": "UMLS:C0334372", "names": ["Papillary DCIS", "DCIS, papillary", "Breast Papillary DCIS", "Intraductal papillary carcinoma", "Intraductal Papillary Carcinoma", "Papillary Ductal Carcinoma In Situ", "Ductal carcinoma in situ, papillary", "Intraductal Papillary Adenocarcinoma", "Intraductal papillary carcinoma, NOS", "Intraductal papillary adenocarcinoma", "Intraductal Papillary Breast Carcinoma", "Breast Intracystic Papillary Carcinoma", "Breast Intraductal Papillary Carcinoma", "breast; intraductal papillary carcinoma", "Non-Invasive Papillary Breast Carcinoma", "breast; carcinoma, intraductal papillary", "Breast Papillary Ductal Carcinoma In Situ", "carcinoma; intraductal, papillary, breast", "intraductal; carcinoma, papillary, breast", "Intraductal papillary adenocarcinoma, NOS", "Non-Infiltrating Papillary Breast Carcinoma", "Intraductal Papillary Breast Adenocarcinoma", "Non-Invasive Papillary Breast Adenocarcinoma", "Non-Invasive Intraductal Papillary Carcinoma", "papillary; adenocarcinoma, intraductal, breast", "adenocarcinoma; intraductal, papillary, breast", "adenocarcinoma; papillary, intraductal, breast", "Noninfiltrating intraductal papillary carcinoma", "Non-Infiltrating Intraductal Papillary Carcinoma", "Non-infiltrating intraductal papillary carcinoma", "Non-Infiltrating Papillary Breast Adenocarcinoma", "Non-Invasive Intraductal Papillary Adenocarcinoma", "Noninfiltrating intraductal papillary adenocarcinoma", "Non-infiltrating intraductal papillary adenocarcinoma", "Non-Infiltrating Intraductal Papillary Adenocarcinoma", "Noninfiltrating intraductal papillary adenocarcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Noninfiltrating intraductal papillary adenocarcinoma (morphologic abnormality)", "shortest_name_length": 14}
{"curie": "MONDO:0800108", "names": ["cleft tricuspid valve", "Cleft leaflet, tricuspid valve", "True cleft of tricuspid leaflet", "Cleft leaflet of tricuspid valve", "cleft leaflet of tricuspid valve", "Cleft leaflet of tricuspid valve (disorder)", "Cleft leaflet of tricuspid valve (diagnosis)", "congenital heart defect malformations tricuspid valve cleft leaflet"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleft leaflet of tricuspid valve", "shortest_name_length": 21}
{"curie": "UMLS:C1336349", "names": ["Stage IVA Nasopharynx Keratinizing Epidermoid Carcinoma", "Stage IVA Keratinizing Epidermoid Carcinoma of Nasopharynx", "Stage IVA Nasopharynx Keratinizing Squamous Cell Carcinoma", "Stage IVA Nasopharyngeal Keratinizing Epidermoid Carcinoma", "Stage IVA Keratinizing Squamous Cell Carcinoma of Nasopharynx", "Stage IVA Nasopharyngeal Keratinizing Squamous Cell Carcinoma", "Stage IVA Keratinizing Epidermoid Carcinoma of the Nasopharynx", "Stage IVA Keratinizing Squamous Cell Carcinoma of the Nasopharynx", "Stage IVA Nasopharyngeal Throat Keratinizing Squamous Cell Cancer", "Stage IVA Nasopharyngeal Keratinizing Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Nasopharyngeal Keratinizing Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 55}
{"curie": "UMLS:C4552296", "names": ["Ocular procedural complication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ocular procedural complication", "shortest_name_length": 30}
{"curie": "MONDO:0002531", "names": ["skin", "Skin tumor", "skin tumor", "Skin Tumor", "tumor skin", "SKIN TUMOR", "skin tumors", "Skin tumour", "SKIN TUMORS", "skin tumour", "tumors skin", "Skin tumors", "Skin cancer", "Skin tumours", "skin tumours", "Skin--Tumors", "NEOPLASM SKIN", "Tumor of skin", "Tumor of Skin", "Skin Neoplasm", "Neoplasm skin", "skin neoplasm", "tumor of skin", "Neoplasm;skin", "skin neoplasms", "Neoplasm, Skin", "Tumour of skin", "Skin tumor NOS", "Skin Neoplasms", "Cutaneous tumor", "Neoplasms, Skin", "cutaneous tumor", "cutaneous tumors", "Neoplasm of skin", "Cutaneous tumour", "Neoplasm of Skin", "neoplasm of skin", "Skin neoplasm NOS", "Tumor of the Skin", "tumor of the skin", "Tumor of the skin", "Cutaneous neoplasm", "Tumour of the skin", "zone of skin tumor", "skin benign neoplasm", "Neoplasm of the Skin", "Neoplasm of the skin", "neoplasm of the skin", "Dermatological tumors", "zone of skin neoplasm", "tumor of zone of skin", "Neoplasia of the skin", "Dermatological tumours", "neoplasm of zone of skin", "neoplasm of skin by site", "Skin cancer (non-melanoma)", "Neoplasm of skin (disorder)", "neoplasm of skin (diagnosis)", "zone of skin neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin neoplasm", "shortest_name_length": 4}
{"curie": "MONDO:0003555", "names": ["Bartholin gland adenosquamous carcinoma", "Bartholin Gland Adenosquamous Carcinoma", "Bartholin's gland adenosquamous carcinoma", "Bartholin's Gland Adenosquamous Carcinoma", "major vestibular gland adenosquamous carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bartholin gland adenosquamous carcinoma", "shortest_name_length": 39}
{"curie": "MONDO:0018616", "names": ["CSC", "CSCR", "Central Serous Retinopathy", "central serous retinopathy", "Central serous retinopathy", "Serous Retinopathy, Central", "retinopathy; central serous", "central serous; retinopathy", "Retinopathy, Central Serous", "Central serous choroidopathy", "Central Serous Retinopathies", "central serous choroidopathy", "Serous Retinopathies, Central", "Retinopathies, Central Serous", "Central serous chorioretinopathy", "CSR - central serous retinopathy", "CSR - Central serous retinopathy", "central serous chorioretinopathy", "Central Serous Chorioretinopathy", "Serous Chorioretinopathy, Central", "chorioretinopathy; central serous", "Chorioretinopathy, Central Serous", "Central Serous Chorioretinopathies", "CSC - Central serous choroidopathy", "choroidoretinopathy; central serous", "Serous Chorioretinopathies, Central", "Chorioretinopathies, Central Serous", "central serous retinopathy (diagnosis)", "Central serous chorioretinopathy (disorder)", "central serous chorioretinopathy after bone marrow transplantation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central serous chorioretinopathy", "shortest_name_length": 3}
{"curie": "MONDO:0013306", "names": ["COXPD7", "Severe C12ORF65-related COXPD", "severe C12ORF65-related COXPD", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7", "combined oxidative phosphorylation deficiency 7", "combined oxidative phosphorylation defect type 7", "Combined oxidative phosphorylation defect type 7", "combined oxidative phosphorylation deficiency type 7", "C12ORF65 combined oxidative phosphorylation deficiency", "C12orf65 combined oxidative phosphorylation deficiency", "COXPD7 - combined oxidative phosphorylation defect type 7", "Combined oxidative phosphorylation defect type 7 (disorder)", "combined oxidative phosphorylation defect type 7 (diagnosis)", "severe C12ORF65-related combined oxidative phosphorylation defect", "Severe C12ORF65-related combined oxidative phosphorylation defect", "combined oxidative phosphorylation deficiency caused by mutation in C12ORF65", "combined oxidative phosphorylation deficiency caused by mutation in C12orf65"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation defect type 7", "shortest_name_length": 6}
{"curie": "MONDO:0033282", "names": ["MMDS5", "ISCA1 deficiency", "MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 5", "multiple mitochondrial dysfunctions syndrome 5", "Multiple mitochondrial dysfunctions syndrome type 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple mitochondrial dysfunctions syndrome 5", "shortest_name_length": 5}
{"curie": "UMLS:C3272838", "names": ["Colorectal Benign Granular Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Benign Granular Cell Tumor", "shortest_name_length": 37}
{"curie": "MONDO:0015813", "names": ["PCMZL", "C-MALT", "salt lymphoma", "SALT Lymphoma", "SALT lymphoma", "Cutaneous Immunocytoma", "cutaneous Immunocytoma", "SALT type B-cell lymphoma", "marginal zone B cell lymphoma of skin", "Marginal Zone B Cell Lymphoma of Skin", "marginal zone B-cell lymphoma of skin", "Skin-associated lymphoid tissue lymphoma", "Skin-Associated Lymphoid Tissue Lymphoma", "skin-associated lymphoid tissue lymphoma", "marginal zone B cell lymphoma of the skin", "Marginal Zone B Cell Lymphoma of the Skin", "primary cutaneous marginal zone B-cell lymphoma", "Primary cutaneous marginal zone B-cell lymphoma", "marginal zone B-cell lymphoma of skin (diagnosis)", "Skin-associated lymphoid tissue type B-cell lymphoma", "Primary cutaneous marginal zone B-cell lymphoma (disorder)", "Primary cutaneous marginal zone B-cell lymphoma (diagnosis)", "Primary cutaneous marginal zone B-cell lymphoma (morphologic abnormality)", "Primary Cutaneous Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue", "Primary cutaneous marginal zone lymphoma of mucosa-associated lymphoid tissue", "Primary Cutaneous Marginal Zone B-Cell Lymphoma of Mucosa-Associated Lymphoid Tissue", "Primary cutaneous marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue", "Primary cutaneous marginal zone B cell lymphoma of mucosa-associated lymphoid tissue", "Primary Cutaneous Marginal Zone B Cell Lymphoma of Mucosa-Associated Lymphoid Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary cutaneous marginal zone B-cell lymphoma", "shortest_name_length": 5}
{"curie": "UMLS:C1333139", "names": ["Complex without cytologic atypia", "Complex endometrial hyperplasia without atypia", "Complex Endometrial Hyperplasia without Atypia", "Complex endometrial hyperplasia without atypia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Complex endometrial hyperplasia without atypia", "shortest_name_length": 32}
{"curie": "MONDO:0015737", "names": ["typical nemaline myopathy", "typical congenital nemaline myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "typical nemaline myopathy", "shortest_name_length": 25}
{"curie": "MONDO:0001635", "names": ["bladder squamous papilloma", "Bladder Squamous Papilloma", "Bladder Keratotic Papilloma", "Bladder Squamous Cell Papilloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder squamous papilloma", "shortest_name_length": 26}
{"curie": "UMLS:C5418915", "names": ["Metastatic Primary Peritoneal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Primary Peritoneal Adenocarcinoma", "shortest_name_length": 44}
{"curie": "MONDO:0021019", "names": ["OA1", "XLOA", "Ocular albinism type 1", "Ocular Albinism Type 1", "Ocular Albinism type 1", "ocular albinism type 1", "Ocular albinism, type I", "ALBINISM, OCULAR, TYPE I", "albinism, ocular, type I", "albinism, ocular, type 1", "ocular albinism x-linked", "X linked ocular albinism", "Albinism, Ocular, Type I", "X-linked ocular albinism", "Nettleship-Falls Syndrome", "Nettleship-Falls syndrome", "OA1 - X-linked ocular albinism", "X-linked recessive ocular albinism", "Ocular albinism, type I (disorder)", "ocular albinism x-linked (diagnosis)", "NETTLESHIP-FALLS TYPE OCULAR ALBINISM", "Nettleship-Falls type ocular albinism", "Ocular albinism, Nettleship-Falls type", "ocular albinism, Nettleship-Falls type", "X-linked ocular albinism, Nettleship type", "ocular albinism, type I, Nettleship-Falls type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked recessive ocular albinism", "shortest_name_length": 3}
{"curie": "MONDO:0015219", "names": ["isolated central nervous system malformation", "nonsyndromic central nervous system malformation", "non-syndromic central nervous system malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-syndromic central nervous system malformation", "shortest_name_length": 44}
{"curie": "MONDO:0008219", "names": ["Pemphigus vulgaris", "Pemphigus Vulgaris", "pemphigus vulgaris", "PEMPHIGUS VULGARIS", "pemphigus; vulgaris", "Pemphigus, vulgaris", "vulgaris; pemphigus", "pemphigus pv vulgaris", "PV - Pemphigus vulgaris", "Familial pemphigus vulgaris", "familial pemphigus vulgaris", "pemphigus vulgaris, familial", "Pemphigus vulgaris, familial", "PEMPHIGUS VULGARIS, FAMILIAL", "Pemphigus vulgaris (disorder)", "pemphigus vulgaris (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pemphigus vulgaris", "shortest_name_length": 18}
{"curie": "MONDO:0032690", "names": ["MIGSB", "MICROCEPHALY, GROWTH DEFICIENCY, SEIZURES, AND BRAIN MALFORMATIONS", "microcephaly, growth deficiency, seizures, and brain malformations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly, growth deficiency, seizures, and brain malformations", "shortest_name_length": 5}
{"curie": "UMLS:C3827733", "names": ["Umbilical cord occlusion", "Umbilical Cord Occlusion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Umbilical cord occlusion", "shortest_name_length": 24}
{"curie": "MONDO:0033636", "names": ["MC4DN4", "mitochondrial complex 4 deficiency, nuclear type 4", "mitochondrial complex IV deficiency, nuclear type 4", "MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 4 deficiency, nuclear type 4", "shortest_name_length": 6}
{"curie": "MONDO:0005298", "names": ["BMND", "osteoporosis", "OSTEOPOROSIS", "Osteoporoses", "Osteoporosis", "Osteoporosis NOS", "Bone rarefaction", "OP - Osteoporosis", "rarefaction; bone", "Osteoporosis, NOS", "Osteoporosis senile", "Senile Osteoporosis", "Senile osteoporosis", "senile osteoporosis", "Senile Osteoporoses", "osteoporosis senile", "senile; osteoporosis", "type ii osteoporosis", "Type II osteoporosis", "Osteoporoses, Senile", "Osteoporosis, Senile", "osteoporosis; senile", "Age-Related Bone Loss", "age related bone loss", "Bone Loss, Age-Related", "Bone Loss, Age Related", "Osteoporosis (disorder)", "Age-Related Bone Losses", "Age related osteoporosis", "Age Related Osteoporosis", "Bone Losses, Age-Related", "age-related osteoporosis", "osteoporosis (diagnosis)", "age related osteoporosis", "Age-Related Osteoporoses", "Unspecified osteoporosis", "Age-related osteoporosis", "Age-Related Osteoporosis", "Osteoporoses, Age-Related", "Osteoporosis, unspecified", "Involutional osteoporosis", "Osteoporosis, Age-Related", "Osteoporosis, Age Related", "Osteoporosis, Involutional", "osteoporosis, involutional", "OSTEOPOROSIS, INVOLUTIONAL", "osteoporosis, postmenopausal", "Senile osteoporosis (disorder)", "senile osteoporosis (diagnosis)", "osteoporosis, susceptibility to", "fracture, hip, susceptibility to", "FRACTURE, HIP, SUSCEPTIBILITY TO", "Unspecified osteoporosis, site unspecified", "osteoporosis, postmenopausal, susceptibility", "BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS", "bone mineral density variation QTL, osteoporosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteoporosis", "shortest_name_length": 4}
{"curie": "MONDO:0010136", "names": ["TDH4", "GDTH IV", "DEIODINASE DEFICIENCY", "Deiodinase Deficiency", "deiodinase deficiency", "Deiodinase deficiency", "Dehalogenase Deficiency", "thyroid dyshormonogenesis 4", "THYROID DYSHORMONOGENESIS 4", "Thyroid Dyshormonogenesis 4", "Iodotyrosine deiodination defect", "thyroid dyshormonogenesis type 4", "Iodotyrosine deiodinase deficiency", "iodotyrosine dehalogenase deficiency", "IODOTYROSINE DEHALOGENASE DEFICIENCY", "Iodotyrosine Dehalogenase Deficiency", "Iodotyrosine dehalogenase deficiency", "Hypothyroidism due to deiodase defect", "IYD familial thyroid dyshormonogenesis", "genetic defect in thyroid hormonogenesis 4", "Iodotyrosine deiodinase deficiency syndrome", "Genetic defect in thyroid hormonogenesis IV", "Iodotyrosine deiodination defect (disorder)", "THYROID HORMONOGENESIS, GENETIC DEFECT IN, 4", "Thyroid Hormonogenesis, Genetic Defect in, 4", "thyroid hormonogenesis, genetic defect in, 4", "Hypothyroidism due to iodotyrosine deiodinase defect", "hypothyroidism, congenital, due to dyshormonogenesis, 4", "Hypothyroidism, Congenital, due to Dyshormonogenesis, 4", "HYPOTHYROIDISM, CONGENITAL, DUE TO DYSHORMONOGENESIS, 4", "familial thyroid dyshormonogenesis caused by mutation in IYD"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid dyshormonogenesis 4", "shortest_name_length": 4}
{"curie": "UMLS:C2825221", "names": ["Left Main Coronary Artery Stenosis, Percentage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Left Main Coronary Artery Stenosis, Percentage", "shortest_name_length": 46}
{"curie": "UMLS:C0275794", "names": ["Staphylococcal pharyngitis", "staphylococcal; pharyngitis", "Pharyngitis, staphylococcal", "pharyngitis; staphylococcal", "Staphylococcal pharyngitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Staphylococcal pharyngitis", "shortest_name_length": 26}
{"curie": "UMLS:C0346208", "names": ["VAIN", "Vaginal SIL", "Vaginal Intraepithelial Tumor", "Intraepithelial Tumor of Vagina", "Vaginal Intraepithelial Neoplasm", "vagina; intraepithelial neoplasia", "VAGINAL INTRAEPITHELIAL NEOPLASIA", "Vaginal Intraepithelial Neoplasia", "Vaginal intraepithelial neoplasia", "Intraepithelial Neoplasm of Vagina", "neoplasia; intraepithelial, vagina", "Intraepithelial Neoplasia of Vagina", "Intraepithelial Tumor of the Vagina", "Intraepithelial Neoplasm of the Vagina", "Vaginal Squamous Intraepithelial Lesion", "Intraepithelial Neoplasia of the Vagina", "VAIN - Vaginal intraepithelial neoplasia", "vaginal neoplasm intraepithelial neoplasia", "Vaginal intraepithelial neoplasia (disorder)", "Vaginal intraepithelial neoplasia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal intraepithelial neoplasia", "shortest_name_length": 4}
{"curie": "UMLS:C1518696", "names": ["Ovarian Dermoid Cyst with Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Dermoid Cyst with Adenocarcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0044208", "names": ["SGD2", "SPECIFIC GRANULE DEFICIENCY 2", "specific granule deficiency 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "specific granule deficiency 2", "shortest_name_length": 4}
{"curie": "MONDO:0024881", "names": ["Secondary Cancer", "secondary cancer", "secondary malignancy", "Secondary Malignancy", "secondary malignant neoplasm", "Secondary Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary malignant neoplasm", "shortest_name_length": 16}
{"curie": "UMLS:C0278496", "names": ["stage II gastric cancer", "Gastric cancer stage II", "gastric cancer stage II", "Stomach cancer stage II", "Stage II Gastric Cancer", "gastric cancer, stage II", "stomach cancer, stage II", "Gastric malignancy stage II", "Stage II Gastric Cancer AJCC v7", "Stage II Gastric (Stomach) Cancer", "malignant tumor of stomach stage II", "malignant neoplasm of stomach stage II", "Malignant neoplasm of stomach stage II", "malignant neoplasm of stomach stage II (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant neoplasm of stomach stage II", "shortest_name_length": 23}
{"curie": "UMLS:C0334458", "names": ["Fascial fibrosarcoma", "fascial fibrosarcoma", "Fascial Fibrosarcoma", "fascial fibrosarcoma (diagnosis)", "Fascial fibrosarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fascial fibrosarcoma", "shortest_name_length": 20}
{"curie": "UMLS:C1377787", "names": ["stage IVB vagina cancer", "Vaginal cancer stage IVB", "Vaginal Cancer Stage IVB", "metastatic vagina cancer", "Stage IVB Vaginal Cancer", "stage IVB vaginal cancer", "vagina cancer, stage IVB", "Vaginal cancer metastatic", "vaginal cancer, stage IVB", "metastatic vaginal cancer", "vagina cancer, metastatic", "Cancer of vagina stage IVB", "vaginal cancer, metastatic", "Cancer of vagina metastatic", "AJCC Stage IVB Vaginal Cancer", "stage IVB cancer of the vagina", "metastatic cancer of the vagina", "cancer of the vagina, stage IVB", "FIGO Stage IVB Vagina Carcinoma", "Stage IVB Vaginal Cancer AJCC v7", "FIGO Stage IVB Vaginal Carcinoma", "cancer of the vagina, metastatic", "Stage IVB Vaginal Cancer AJCC v6", "stage IVB carcinoma of the vagina", "metastatic carcinoma of the vagina", "carcinoma of the vagina, stage IVB", "FIGO Stage IVB Carcinoma of Vagina", "carcinoma of the vagina, metastatic", "Stage IVB Vaginal Carcinoma AJCC v6", "Stage IVB Vaginal Carcinoma AJCC v7", "FIGO Stage IVB Carcinoma of the Vagina", "Stage IVB Vaginal Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Vaginal Cancer AJCC v6 and v7", "shortest_name_length": 23}
{"curie": "MONDO:0002592", "names": ["Invasive Thymoma", "invasive thymoma", "Infiltrating Thymoma", "infiltrating thymoma", "Thymoma malignant Invasive", "Thymoma Malignant Invasive", "Invasive Malignant Thymoma", "thymoma malignant invasive", "invasive malignant thymoma", "Thymoma malignant invasive", "malignant thymoma, invasive", "Malignant Thymoma, Invasive", "invasive thymoma and thymic carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "invasive malignant thymoma", "shortest_name_length": 16}
{"curie": "UMLS:C1333843", "names": ["Grade 3 Invasive Breast Carcinoma", "Grade 3 Infiltrating Breast Carcinoma", "Unfavorable Infiltrating Breast Carcinoma", "Poorly Differentiated Invasive Breast Carcinoma", "Poorly Differentiated Infiltrating Breast Carcinoma", "High Combined Histologic Grade Infiltrating Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade 3 Invasive Breast Carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0018008", "names": ["IGCM", "idiopathic giant cell myocarditis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic giant cell myocarditis", "shortest_name_length": 4}
{"curie": "MONDO:0011359", "names": ["AFND", "Toriello syndrome", "Toriello syndrome II", "frontonasal dysplasia acromelic", "acromelic frontonasal dysplasia", "Acromelic frontonasal dysplasia", "Acromelic Frontonasal Dysostosis", "acromelic frontonasal dysostosis", "ACROMELIC FRONTONASAL DYSOSTOSIS", "Acromelic frontonasal dysostosis", "Acromelic frontonasal dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acromelic frontonasal dysostosis", "shortest_name_length": 4}
{"curie": "MONDO:0014249", "names": ["MFAB", "mammary polyadenomatosis", "Multiple fibroadenomas of breast", "multiple fibroadenoma of the breast", "MULTIPLE FIBROADENOMAS OF THE BREAST", "multiple fibroadenomas of the breast", "Multiple fibroadenomas of breast (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple fibroadenoma of the breast", "shortest_name_length": 4}
{"curie": "MONDO:0010789", "names": ["mela", "melas", "MELAS", "mela syndrome", "MELAS Syndrome", "MELAS syndrome", "MELAS SYNDROME", "syndrome melas", "melas syndrome", "Syndrome, MELAS", "Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke", "mitochondrial encephalomyopathy, lactic acidosis and stroke", "Mitochondrial Myopathy, Lactic Acidosis, Stroke-Like Episode", "Juvenile myopathy, encephalopathy, lactic acidosis and stroke", "Juvenile myopathy, encephalopathy, lactic acidosis AND stroke", "Myopathy, Mitochondrial-Encephalopathy-Lactic Acidosis-Stroke", "Mitochondrial encephalopathy, lactic acidosis and stroke-like episodes", "Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes", "Juvenile myopathy, encephalopathy, lactic acidosis AND stroke (disorder)", "mitochondrial encephalomyopathy lactic acidosis and stroke-like episodes", "Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes", "mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes", "Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes", "Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes", "mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS)", "MELAS - Mitochondrial encephalopathy, lactic acidosis and stroke-like episodes", "mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes", "Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes", "Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, And Stroke-Like Episodes", "mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes", "MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES", "MELAS - Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes", "mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MELAS syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0863193", "names": ["Stage IV Gastric Cancer without Metastasis", "Stomach Carcinoma Stage IV without Metastasis", "Gastric carcinoma stage IV without metastases", "Gastric Carcinoma Stage IV without Metastasis", "Stomach carcinoma stage IV without metastases", "Gastric Carcinoma, Stage IV Without Metastases", "Carcinoma of Stomach Stage IV without Metastasis", "Carcinoma of the Stomach Stage IV without Metastasis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric carcinoma stage IV without metastases", "shortest_name_length": 42}
{"curie": "MONDO:0013729", "names": ["RPRGL3", "PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 3", "ANXA5 pregnancy loss, recurrent, susceptibility", "pregnancy loss, recurrent, susceptibility to, 3", "pregnancy loss, recurrent, susceptibility to, type 3", "pregnancy loss, recurrent, susceptibility caused by mutation in ANXA5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pregnancy loss, recurrent, susceptibility to, 3", "shortest_name_length": 6}
{"curie": "UMLS:C1608408", "names": ["Malignant transformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant transformation", "shortest_name_length": 24}
{"curie": "MONDO:0021100", "names": ["Breast Tumor", "Breast tumor", "breast tumor", "breast tumour", "Tumor, Breast", "mammary tumor", "Breast tumour", "breast tumors", "Breast Tumors", "Breast--Tumors", "breast tumours", "Tumors, Breast", "Tumor of breast", "breast neoplasm", "Tumor of Breast", "Breast Neoplasm", "BREAST NEOPLASM", "Neoplasm breast", "NEOPLASM BREAST", "tumor of breast", "Breast neoplasm", "Tumour of breast", "Breast Neoplasms", "neoplasm, breast", "Neoplasm, Breast", "breast neoplasms", "Neoplasms, Breast", "Mammary Neoplasms", "Neoplasm of Breast", "Neoplasm of breast", "neoplasm of breast", "Tumor of the Breast", "Breast neoplasm NOS", "tumor of the breast", "Tumours of the breast", "Neoplasm of the Breast", "Neoplasm of the breast", "neoplasm of the breast", "Neoplasia of the breast", "breast neoplasm diagnosis", "breast neoplasm (disease)", "Neoplasm of breast (disorder)", "location of neoplasm of breast", "neoplasm of breast (diagnosis)", "location of neoplasm of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast neoplasm", "shortest_name_length": 12}
{"curie": "MONDO:0033365", "names": ["DEE56", "EIEE56", "infantile epileptic encephalopathy 56", "early infantile epileptic encephalopathy 56", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 56", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 56", "developmental and epileptic encephalopathy 56", "epileptic encephalopathy, early infantile, 56", "developmental and epileptic encephalopathy, 56"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 56", "shortest_name_length": 5}
{"curie": "MONDO:0000227", "names": ["Kenya; fever", "fever; Kenya", "Kenya tick typhus", "Kenyan tick typhus", "African tick typhus", "AFRICAN TICK TYPHUS", "spotted fever; Kenya", "Kenya; spotted fever", "African Tick Bite Fever", "African tick bite fever", "African Tick-Bite Fever", "African tick-bite fever", "Tick-Bite Fever, African", "African tick-borne fever", "Fever, African Tick-Bite", "South African tick fever", "South African tick typhus", "Rickettsia africae Infection", "Rickettsia africae Infections", "Infection, Rickettsia africae", "Kenya tick typhus (diagnosis)", "South African tick-bite fever", "south african tick-bite fever", "FEVER, SOUTH AFRICAN TICK BITE", "South African; tick-bite fever", "Infections, Rickettsia africae", "tick-bite; fever, South African", "Rickettsia africae spotted fever", "African tick bite fever (disorder)", "South African tick fever (diagnosis)", "South African tick-bite fever (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "African tick-bite fever", "shortest_name_length": 12}
{"curie": "MONDO:0003113", "names": ["extragonadal germ cell cancer", "tumor of extragonadal germ cell", "neoplasm of Extragonadal germ cell", "malignant extragonadal germ cell tumor", "extragonadal germ cell malignant tumor", "Malignant Extragonadal Germ Cell Tumor", "extragonadal germ cell tumor, malignant", "Malignant Tumor of Extragonadal Germ Cell", "malignant tumor of extragonadal germ cell", "Malignant Neoplasm of Extragonadal Germ Cell", "malignant neoplasm of extragonadal germ cell", "Malignant Tumor of the Extragonadal Germ Cell", "malignant tumor of the extragonadal germ cell", "malignant neoplasm of the extragonadal germ cell", "Malignant Neoplasm of the Extragonadal Germ Cell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extragonadal germ cell cancer", "shortest_name_length": 29}
{"curie": "MONDO:0014060", "names": ["RDCCAS", "retinol dystrophy-iris coloboma-comedogenic acne syndrome", "progressive retinal dystrophy due to retinol transport defect", "retinal dystrophy, iris coloboma, and comedogenic acne syndrome", "RETINAL DYSTROPHY, IRIS COLOBOMA, AND COMEDOGENIC ACNE SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive retinal dystrophy due to retinol transport defect", "shortest_name_length": 6}
{"curie": "UMLS:C5670414", "names": ["Unresectable Primary Peritoneal Endometrioid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Primary Peritoneal Endometrioid Adenocarcinoma", "shortest_name_length": 59}
{"curie": "MONDO:0024676", "names": ["Wilms tumor", "Wilms Tumor", "kidney Wilms tumor", "Childhood Wilms Tumor", "childhood Wilms tumor", "Childhood Renal Wilms Tumor", "childhood renal Wilms tumor", "Childhood Kidney Wilms Tumor", "childhood kidney Wilms tumor", "Childhood Renal Wilms' Tumor", "childhood renal Wilms' tumor", "Childhood Kidney Nephroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood kidney Wilms tumor", "shortest_name_length": 11}
{"curie": "MONDO:0009437", "names": ["BAMLAZ", "Bamforth syndrome", "BAMFORTH SYNDROME", "Bamforth-Lazarus syndrome", "BAMFORTH-LAZARUS SYNDROME", "Bamforth Lazarus syndrome", "Hypothyroidism cleft palate", "Hypothyroidism-cleft palate syndrome", "Bamforth Lazarus syndrome (disorder)", "hypothyroidism-cleft palate syndrome", "Hypothyroidism and cleft palate syndrome", "Athyroidal hypothyroidism-spiky hair-cleft palate syndrome", "HYPOTHYROIDISM, ATHYROIDAL, WITH SPIKY HAIR AND CLEFT PALATE", "hypothyroidism, ATHYROIDAL, with spiky hair and cleft palate", "Hypothyroidism, athyroidal, with spiky hair and cleft palate", "Athyroidal hypothyroidism with spiky hair and cleft palate syndrome", "hypothyroidism, thyroidal or ATHYROIDAL, with spiky hair and cleft palate", "HYPOTHYROIDISM, THYROIDAL OR ATHYROIDAL, WITH SPIKY HAIR AND CLEFT PALATE", "hypothyroidism cleft palate hypothyroidism, athyroidal, with spiky hair and cleft palate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bamforth-Lazarus syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0044997", "names": ["midbrain disease", "midbrain disorder", "Midbrain disorder", "disease of midbrain", "disorder of midbrain", "Disorder of midbrain", "Midbrain disorder, NOS", "Disease of midbrain, NOS", "midbrain disease or disorder", "Disorder of midbrain (disorder)", "disease or disorder of midbrain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "midbrain disorder", "shortest_name_length": 16}
{"curie": "MONDO:0007280", "names": ["CCV", "CTRCT8", "cataract 8 multiple types", "cataract 8, multiple types", "CATARACT 8, MULTIPLE TYPES", "cataract congenital Volkmann type", "Cataract congenital Volkmann type", "Cataract, Congenital, Volkmann Type", "cataract, congenital, Volkmann type", "CATARACT, CONGENITAL, VOLKMANN TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 8 multiple types", "shortest_name_length": 3}
{"curie": "UMLS:C3273010", "names": ["IHCA", "Telangiectatic Adenoma", "Inflammatory Hepatocellular Adenoma", "Telangiectatic Hepatocellular Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Inflammatory Hepatocellular Adenoma", "shortest_name_length": 4}
{"curie": "MONDO:0044763", "names": ["diarrhea from decreased bowel motility", "diarrheal disease secondary to decreased bowel motility"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diarrheal disease secondary to decreased bowel motility", "shortest_name_length": 38}
{"curie": "UMLS:C4764226", "names": ["Refractory Desmoplastic Small Round Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Desmoplastic Small Round Cell Tumor", "shortest_name_length": 46}
{"curie": "MONDO:0008289", "names": ["T1P", "BSVD", "ADT1P", "BSVD1", "POREN1", "T1P, FORMERLY", "porencephaly 1", "ADT1P, FORMERLY", "GOULD SYNDROME 1", "POREN1, FORMERLY", "Type 1 Porencephaly", "Porencephaly Type 1", "porencephaly type 1", "COL4A1 porencephaly", "Porencephaly, Type 1", "Familial Porencephaly", "infantile hemiparesis", "Porencephaly, Familial", "PORENCEPHALY 1, FORMERLY", "brain small vessel disease 1", "PORENCEPHALY, TYPE 1, FORMERLY", "Familial vascular leukoencephalopathy", "Infantile Hemiplegia with Porencephaly", "Autosomal Dominant Porencephaly Type 1", "HEMIPLEGIA, INFANTILE, WITH PORENCEPHALY", "porencephaly, type 1, autosomal dominant", "Porencephaly, Type 1, Autosomal Dominant", "hemiplegia, infantile, with porencephaly", "Col4a1-Related Brain Small-Vessel Disease", "Col4a1 Related Brain Small Vessel Disease", "porencephaly caused by mutation in COL4A1", "Brain Small Vessel Disease with Hemorrhage", "brain small vessel disease with hemorrhage", "BRAIN SMALL VESSEL DISEASE WITH HEMORRHAGE", "Brain Small-Vessel Disease with Hemorrhage", "Familial Porencephalic White Matter Disease", "Leukoencephalopathy with Axenfeld-Rieger Anomaly", "Leukoencephalopathy with Axenfeld Rieger Anomaly", "LEUKOENCEPHALOPATHY WITH AXENFELD-RIEGER ANOMALY", "leukoencephalopathy with Axenfeld-Riegar anomaly", "leukoencephalopathy with axenfeld-rieger anomaly", "PORENCEPHALY, TYPE 1, AUTOSOMAL DOMINANT, FORMERLY", "COL4A1-related familial vascular leukoencephalopathy", "[OBSOLETE] Brain Small Vessel Disease with Hemorrhage", "Brain Small Vessel Disease With Axenfeld-Rieger Anomaly", "Brain Small Vessel Disease With Axenfeld Rieger Anomaly", "BRAIN SMALL VESSEL DISEASE WITH AXENFELD-RIEGER ANOMALY", "brain small vessel disease with Axenfeld-Riegar anomaly", "brain small vessel disease with axenfeld-rieger anomaly", "COL4A1-related brain small vessel disease with hemorrhage", "brain small vessel disease with or without ocular anomalies", "BRAIN SMALL VESSEL DISEASE 1 WITH OR WITHOUT OCULAR ANOMALIES", "hemiplegia, infantile, with porencephaly porencephaly, type 1", "brain small vessel disease 1 with or without ocular anomalies", "autosomal dominant retinal arteriolar tortuosity, infantile hemiparesis, and leukencephalopathy", "RETINAL ARTERIOLAR TORTUOSITY, INFANTILE HEMIPARESIS, AND LEUKOENCEPHALOPATHY, AUTOSOMAL DOMINANT", "retinal arteriolar tortuosity, infantile hemiparesis, and leukoencephalopathy, autosomal dominant", "Retinal Arteriolar Tortuosity, Infantile Hemiparesis, and Leukoencephalopathy, Autosomal Dominant", "COL4A1-related retinal arteriolar tortuosity-infantile hemiparesis-autosomal dominant leukoencephalopathy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brain small vessel disease 1 with or without ocular anomalies", "shortest_name_length": 3}
{"curie": "UMLS:C0751025", "names": ["Rolandic Type Cerebral Palsy", "Cerebral Palsy, Rolandic Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebral Palsy, Rolandic Type", "shortest_name_length": 28}
{"curie": "MONDO:0020235", "names": ["lens size anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lens size anomaly", "shortest_name_length": 17}
{"curie": "UMLS:C0023886", "names": ["Hepatic Amebiasis", "Hepatic amebiasis", "hepatic amebiasis", "Amebiasis, Hepatic", "hepatic amoebiasis", "hepatic; amebiasis", "Hepatic Amoebiasis", "amebiasis; hepatic", "Hepatic amoebiasis", "Amoebiasis, Hepatic", "abscess amebic liver", "Amebic liver abscess", "Amebic Liver Abscess", "amebic liver abscess", "Liver Abscess, Amebic", "Amoebic Liver Abscess", "abscess amoebic liver", "Abscess, Amebic Liver", "LIVER ABSCESS AMOEBIC", "Amoebic liver abscess", "amoebic liver abscess", "Liver abscess, Amebic", "Abscess, Liver, Amebic", "Abscess, Amoebic Liver", "Amebic liver infection", "Amebic Liver Abscesses", "LIVER, ABSCESS, AMEBIC", "Liver Abscess, Amoebic", "Liver Abscesses, Amebic", "Amebic abscess of liver", "Amoebic Liver Abscesses", "Amoebic Hepatic Abscess", "Abscesses, Amebic Liver", "Abscess, Hepatic, Amebic", "Abscess, Amebic, Hepatic", "Hepatic Abscess, Amoebic", "Abscesses, Amoebic Liver", "Abscess, Amoebic Hepatic", "Liver Abscesses, Amoebic", "Amoebic Hepatic Abscesses", "Abscesses, Amoebic Hepatic", "Hepatic Abscesses, Amoebic", "ALA - Amebic liver abscess", "ALA - Amoebic liver abscess", "Amebic liver abscess (disorder)", "amebic liver abscess (diagnosis)", "Entameba histolytica liver abscess", "Entamoeba histolytica liver abscess"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liver Abscess, Amebic", "shortest_name_length": 17}
{"curie": "UMLS:C0042135", "names": ["uterus atony", "ATONY UTERINE", "Uterine Atony", "inertia uteri", "Uterine atony", "uterine atony", "Atony uterine", "INERTIA UTERI", "atony; uterus", "Inertia uteri", "UTERINE ATONY", "UTERUS, ATONY", "Atonic uterus", "atony uterine", "Uterine atonia", "uterine atonia", "Atony, Uterine", "uterus; atonic", "Uterus atony of", "inertia; uterus", "Atony of uterus", "atony of uterus", "uterus; inertia", "Uterine inertia", "Uterine Inertia", "UTERUS ATONY OF", "uterine inertia", "inertia uterine", "Inertia, Uterine", "Poor contractions", "poor; contractions", "contractions; poor", "Atony of uterus NOS", "Uterine inertia NOS", "Uterine inertia, NOS", "atony of gravid uterus", "Hypotonic contractions", "Poor labor contractions", "Hypotonic uterine action", "Poor labour contractions", "poor uterine contractions", "Uterine inertia (disorder)", "Atony of uterus (disorder)", "Hypotonic uterine activity", "uterine inertia (diagnosis)", "atony of uterus (diagnosis)", "Inadequate uterine activity", "Inefficient uterine activity", "Uterine contraction, hypotonic", "contraction; uterus, hypotonic", "uterus; contraction, hypotonic", "poor uterine contractions (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Inertia", "shortest_name_length": 12}
{"curie": "MONDO:0001138", "names": ["intestine angiodysplasia", "angiodysplasia intestine", "angiodysplasia intestines", "Angiodysplasia of intestine", "angiodysplasia of intestine", "Intestinal vascular dysplasia", "Angiodysplasia of intestine (disorder)", "Angiodysplasia of intestinal tract, NOS", "Angiodysplasia of intestine without mention of hemorrhage", "Angiodysplasia of intestine (without mention of hemorrhage)", "Angiodysplasia of intestine (without mention of haemorrhage)", "Localized arteriovenous malformations of intestinal tract, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angiodysplasia of intestine", "shortest_name_length": 24}
{"curie": "MONDO:0005887", "names": ["oral tuberculosis", "Oral tuberculosis", "Oral Tuberculoses", "Oral Tuberculosis", "Tuberculoses, Oral", "Tuberculosis, Oral", "Oral tuberculosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oral tuberculosis", "shortest_name_length": 17}
{"curie": "UMLS:C5205964", "names": ["Seminal Vesicle Soft Tissue Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Seminal Vesicle Soft Tissue Neoplasm", "shortest_name_length": 36}
{"curie": "UMLS:C5205404", "names": ["Recurrent Malignant Ovarian Granulosa Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Malignant Ovarian Granulosa Cell Tumor", "shortest_name_length": 48}
{"curie": "MONDO:0017990", "names": ["CPVT", "CPVT1", "VTSIP", "syncopal paroxysmal tachycardia", "multifocal ventricular premature beats", "double tachycardia induced by catecholamines", "Malignant paroxysmal ventricular tachycardia", "familial polymorphic ventricular tachycardia", "malignant paroxysmal ventricular tachycardia", "Polymorphic catecholergic ventricular tachycardia", "polymorphic catecholergic ventricular tachycardia", "stress-induced polymorphic ventricular tachycardia", "bidirectional tachycardia induced by catecholamine", "VENTRICULAR TACHYCARDIA, STRESS-INDUCED POLYMORPHIC", "Bidirectional Tachycardia Induced By Catecholamines", "Catecholaminergic polymorphic ventricular tachycardia", "catecholaminergic polymorphic ventricular tachycardia", "CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR TACHYCARDIA", "Catecholaminergic Polymorphic Ventricular Tachycardia", "ventricular tachycardia, catecholaminergic polymorphic", "catecholamine-induced polymorphic ventricular tachycardia", "VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1", "Ventricular Tachycardia, Catecholaminergic Polymorphic, 1", "Catecholamine-induced polymorphic ventricular tachycardia", "Catecholaminergic Polymorphic Ventricular Tachycardia Type 1", "Polymorphic ventricular tachycardia induced by catecholamines", "Bidirectional ventricular tachycardia induced by catecholamine", "Catecholaminergic polymorphic ventricular tachycardia (disorder)", "VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder)", "Catecholaminergic Polymorphic Ventricular Tachycardia by ECG Finding", "Catecholaminergic Polymorphic Ventricular Tachycardia by EKG Finding", "VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "catecholaminergic polymorphic ventricular tachycardia", "shortest_name_length": 4}
{"curie": "UMLS:C4288011", "names": ["Vulvar Cloacogenic Carcinoma", "Vulvar Cloacogenic Adenocarcinoma", "Vulvar Adenocarcinoma, Intestinal-Type", "Vulvar Adenocarcinoma of Intestinal Type", "Primary Villoglandular Mucinous Adenocarcinoma Arising in the Surface Epithelium of the Vulva"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Adenocarcinoma, Intestinal-Type", "shortest_name_length": 28}
{"curie": "MONDO:0013390", "names": ["LGMD2Q", "LGMDR17", "LGMD type 2Q", "Plectin-related LGMD R17", "limb-girdle muscular dystrophy type 2Q", "Limb-girdle muscular dystrophy type 2Q", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q", "muscular dystrophy, limb-girdle, type 2Q", "Plectin-related limb-girdle muscular dystrophy R17", "muscular dystrophy, limb-girdle, autosomal recessive 17", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 17", "Autosomal recessive limb girdle muscular dystrophy type 2Q", "autosomal recessive limb-girdle muscular dystrophy type 2Q", "Autosomal recessive limb-girdle muscular dystrophy type 2Q", "Autosomal recessive limb girdle muscular dystrophy type 2Q (disorder)", "autosomal recessive limb-girdle muscular dystrophy due to plectin deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive limb-girdle muscular dystrophy type 2Q", "shortest_name_length": 6}
{"curie": "MONDO:0015382", "names": ["lower lip fistula", "lower lip cysts and fistulae of the face and oral cavity", "cysts and fistulae of the face and oral cavity of lower lip"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lower lip fistula", "shortest_name_length": 17}
{"curie": "UMLS:C4682568", "names": ["Stage IA Uterine Corpus Endometrial Stromal Sarcoma", "Stage IA Uterine Corpus Endometrial Stromal Sarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Uterine Corpus Endometrial Stromal Sarcoma AJCC v8", "shortest_name_length": 51}
{"curie": "MONDO:0014483", "names": ["RDGCA", "retinal dystrophy with inner nuclear layer and ganglion cell anomalies", "retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies", "retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities", "Retinal Dystrophy with Inner Retinal Dysfunction and Ganglion Cell Abnormalities", "RETINAL DYSTROPHY WITH INNER RETINAL DYSFUNCTION AND GANGLION CELL ABNORMALITIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies", "shortest_name_length": 5}
{"curie": "MONDO:0005163", "names": ["simian immunodeficiency virus infection", "Simian immunodeficiency virus infectious disease", "Simian immunodeficiency virus disease or disorder", "Simian immunodeficiency virus caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "simian immunodeficiency virus infection", "shortest_name_length": 39}
{"curie": "MONDO:0018197", "names": ["mtDNA depletion syndrome, hepatocerebrorenal form", "mitochondrial DNA depletion syndrome, hepatocerebrorenal form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial DNA depletion syndrome, hepatocerebrorenal form", "shortest_name_length": 49}
{"curie": "UMLS:C4329267", "names": ["Acute Megakaryoblastic Leukemia with NUP98-KDM5A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Megakaryoblastic Leukemia with NUP98-KDM5A", "shortest_name_length": 48}
{"curie": "MONDO:0010760", "names": ["XH antigen", "XH ANTIGEN", "Xh antigen", "Xh antigen phenotype"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "XH antigen", "shortest_name_length": 10}
{"curie": "UMLS:C1336980", "names": ["Vulvar Non-Neoplastic Disease", "Vulvar Non-Neoplastic Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Non-Neoplastic Disorder", "shortest_name_length": 29}
{"curie": "UMLS:C0016659", "names": ["close fracture", "Closed Fracture", "Closed fracture", "Fracture-closed", "closed fracture", "closed fractures", "CLOSED FRACTURES", "Fracture, Closed", "Closed Fractures", "Fracture, closed", "Fractures, Closed", "closed bone fracture", "Fracture, closed, NOS", "Closed fracture of bone", "closed bone fracture (diagnosis)", "Closed fracture of bone (disorder)", "Fracture of unspecified bone, closed", "Fracture, closed (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fractures, Closed", "shortest_name_length": 14}
{"curie": "UMLS:C0936256", "names": ["Lysine Alpha Ketoglutarate Reductase Deficiency Disease", "Lysine Alpha-Ketoglutarate Reductase Deficiency Disease", "Deficiency Disease, Lysine Alpha-Ketoglutarate Reductase", "Deficiency Disease, Lysine Alpha Ketoglutarate Reductase"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lysine Alpha-Ketoglutarate Reductase Deficiency Disease", "shortest_name_length": 55}
{"curie": "UMLS:C1336303", "names": ["Stage II Nodular Sclerosis Hodgkin Lymphoma", "Hodgkin's disease nodular sclerosis stage II", "Stage II Nodular Sclerosis Hodgkin's Disease", "Nodular Sclerosis Hodgkin's Disease Stage II", "Nodular Sclerosis Hodgkin's Lymphoma Stage II", "Stage II Nodular Sclerosis Hodgkin's Lymphoma", "Stage II Nodular Sclerosis Classical Hodgkin Lymphoma", "Hodgkin's disease nodular sclerosis stage II site unspecified", "Ann Arbor Stage II Nodular Sclerosis Classic Hodgkin Lymphoma", "Ann Arbor Stage II Nodular Sclerosis Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's disease nodular sclerosis stage II", "shortest_name_length": 43}
{"curie": "UMLS:C0085621", "names": ["SPASTIC PARALYSIS", "paralysis spastic", "PARALYSIS SPASTIC", "Spastic paralysis", "Paralysis spastic", "spastic paralysis", "spastic; paralysis", "paralysis; spastic", "Spastic paralysis, NOS", "Spastic paralysis (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spastic paralysis", "shortest_name_length": 17}
{"curie": "UMLS:C1699142", "names": ["Cecal hemorrhage", "Cecal Hemorrhage", "Caecal haemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cecal Hemorrhage", "shortest_name_length": 16}
{"curie": "MONDO:0010931", "names": ["VDDR2B", "Vitamin D Resistant Rickets", "vitamin D resistant rickets", "Vitamin D Dependent Rickets 2b", "vitamin D dependent rickets 2b", "vitamin D-dependent rickets type 2B", "vitamin D-dependent rickets, type 2B", "VDDR IIb - Vitamin D-dependent rickets IIb", "Vitamin D Receptor Signaling Defect Rickets", "vitamin D receptor signaling defect rickets", "Vitamin D-dependent rickets type II without alopecia", "vitamin D-dependent rickets type II without alopecia", "Vitamin D-dependent rickets type II without alopecia (disorder)", "VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR", "Vitamin D-Dependent Rickets, Type 2B, With Normal Vitamin D Receptor", "vitamin D-dependent rickets, type 2B, with normal vitamin D receptor", "hereditary 1,25 dihydroxyvitamin D-resistant rickets with abnormal vitamin D receptor without alopecia", "Hereditary 1,25 Dihydroxyvitamin D-Resistant Rickets with Abnormal Vitamin D Receptor without Alopecia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitamin D-dependent rickets, type 2B", "shortest_name_length": 6}
{"curie": "MONDO:0800132", "names": ["AIPCS", "AUTOINFLAMMATORY-PANCYTOPENIA SYNDROME", "autoinflammatory-pancytopenia syndrome due to DNASE2 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoinflammatory-pancytopenia syndrome due to DNASE2 deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C4054682", "names": ["LH-producing Adenoma", "LH-Producing Pituitary Gland Adenoma", "Luteinizing Hormone-Producing Adenoma", "LH-Producing Pituitary Neuroendocrine Tumor", "Luteinizing Hormone-Producing Gonadotroph Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "LH-Producing Pituitary Neuroendocrine Tumor", "shortest_name_length": 20}
{"curie": "UMLS:C0338479", "names": ["Symptomatic myoclonic epilepsy", "Symptomatic Myoclonic Epilepsy", "Myoclonic Epilepsy, Symptomatic", "Epilepsy, Symptomatic Myoclonic", "Symptomatic Myoclonic Epilepsies", "Myoclonic Epilepsies, Symptomatic", "Epilepsies, Symptomatic Myoclonic", "Symptomatic myoclonic epilepsy (disorder)", "epilepsy generalized symptomatic myoclonic", "Symptomatic myoclonic epilepsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Symptomatic Myoclonic Epilepsy", "shortest_name_length": 30}
{"curie": "UMLS:C0852683", "names": ["Glomerular Disease", "Glomerular disease", "Glomerular vascular disorder", "Glomerular Vascular Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Glomerular vascular disorder", "shortest_name_length": 18}
{"curie": "MONDO:0002427", "names": ["cerebellar disease", "Cerebellum Disease", "Cerebellar disease", "Cerebellar Disease", "cerebellum disease", "CEREBELLAR SYNDROME", "Cerebellar syndrome", "cerebellar diseases", "Cerebellum Diseases", "Cerebellar Disorder", "Cerebellar Diseases", "Cerebellar disorder", "Disease, Cerebellum", "Cerebellar Syndrome", "Syndrome cerebellar", "cerebellar disorder", "Disease, Cerebellar", "SYNDROME CEREBELLAR", "cerebellum diseases", "cerebellar syndrome", "Cerebellum--Diseases", "syndrome; cerebellar", "cerebellar disorders", "Disorder, Cerebellar", "Syndrome, Cerebellar", "Cerebellar Disorders", "Cerebellar Syndromes", "cerebellar; syndrome", "disease of cerebellum", "disorder of cerebellum", "CEREBELLAR DYSFUNCTION", "Cerebellar Dysfunction", "cerebellar dysfunction", "Cerebellar dysfunction", "Cerebellar Dysfunctions", "Dysfunction, Cerebellar", "Cerebellar disorder NOS", "Cerebellar syndrome, NOS", "cerebellum disease or disorder", "Cerebellar disorder (disorder)", "Cerebellar deficiency syndrome", "disease or disorder of cerebellum", "Cerebellar deficiency syndrome, NOS", "Cerebellar deficiency syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellar disorder", "shortest_name_length": 18}
{"curie": "UMLS:C5418994", "names": ["Metastatic Primary Central Chondrosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Primary Central Chondrosarcoma", "shortest_name_length": 41}
{"curie": "UMLS:C2981253", "names": ["Stage IVC Sinonasal Cancer AJCC v7", "Stage IVC Sinonasal Carcinoma AJCC v7", "Stage IVC Nasal Cavity and Paranasal Sinus Cancer", "Stage IVC Nasal Cavity and Paranasal Sinus Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Nasal Cavity and Paranasal Sinus Cancer AJCC v7", "shortest_name_length": 34}
{"curie": "MONDO:0021301", "names": ["Nipple Adenoma", "nipple adenoma", "adenoma; nipple", "adenomas nipple", "nipple; adenoma", "Adenoma of nipple", "Adenoma of Nipple", "adenoma of nipple", "Adenoma of the nipple", "adenoma of the nipple", "Adenoma of the Nipple", "Erosive Nipple Adenomatosis", "Adenoma of nipple (disorder)", "subareolar duct papillomatosis", "Subareolar Duct Papillomatosis", "Subareolar duct papillomatosis", "papillomatosis, subareolar duct", "Adenoma of the nipple (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenoma of nipple", "shortest_name_length": 14}
{"curie": "MONDO:0006245", "names": ["Hidradenocarcinoma", "hidradenocarcinoma", "Clear Cell Eccrine Carcinoma", "clear cell eccrine carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hidradenocarcinoma", "shortest_name_length": 18}
{"curie": "MONDO:0008222", "names": ["ATS", "LQT7", "ANDERSEN SYNDROME", "Andersen syndrome", "Andersen Syndrome", "long QT syndrome 7", "LONG QT SYNDROME 7", "Syndrome, Andersen", "Long QT Syndrome 7", "Long QT syndrome 7", "ANDERSEN-TAWIL SYNDROME", "long QT syndrome type 7", "Andersen-Tawil syndrome", "Andersen-Tawil Syndrome", "Long QT syndrome type 7", "Andersen Tawil Syndrome", "Andersen Tawil syndrome", "Syndrome, Andersen Tawil", "Andersen Tawil syndrome (disorder)", "Andersen-Tawil syndrome (diagnosis)", "Potassium-sensitive cardiodysrhythmic type", "Potassium-Sensitive Cardiodysrhythmic Type", "Andersen Cardiodysrythmic Periodic Paralysis", "Andersen Cardiodysrhythmic Periodic Paralysis", "Andersen cardiodysrhythmic periodic paralysis", "ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS", "cardiodysrhythmic potassium-sensitive periodic paralysis", "Periodic Paralysis, Potassium Sensitive Cardiodysrhythmic Type", "Periodic paralysis, potassium-sensitive cardiodysrhythmic type", "PERIODIC PARALYSIS, POTASSIUM-SENSITIVE CARDIODYSRHYTHMIC TYPE", "Periodic Paralysis, Potassium-Sensitive Cardiodysrhythmic Type", "periodic paralysis, Potassium-sensitive cardiodysrhythmic type", "Potassium-Sensitive Periodic Paralysis, Ventricular Ectopy, and Dysmorphic Features", "Potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Andersen-Tawil syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0010209", "names": ["XAN1", "XO deficiency", "XDH Deficiency", "XDH DEFICIENCY", "XOR deficiency", "XDH deficiency", "xanthinuria type I", "type 1 xanthinuria", "xanthinuria type 1", "Xanthinuria type I", "xanthinuria, type I", "xanthinuria, type 1", "Xanthinuria, Type I", "XANTHINURIA, TYPE I", "Classical xanthinuria", "xanthine oxidase deficiency", "Xanthine Oxidase Deficiency", "XANTHINE OXIDASE DEFICIENCY", "Xanthine oxidase deficiency", "Hereditary xanthinuria type 1", "Hereditary xanthinuria, type I", "hereditary xanthinuria, type I", "Deficiency of xanthine oxidase", "Xanthine Dehydrogenase Deficiency", "XANTHINE DEHYDROGENASE DEFICIENCY", "Xanthine dehydrogenase deficiency", "xanthine dehydrogenase deficiency", "xanthine oxidoreductase deficiency", "Deficiency of hypoxanthine oxidase", "Xanthine oxidoreductase deficiency", "isolated xanthine oxidase deficiency", "Isolated xanthine oxidase deficiency", "Reduced xanthine dehydrogenase level", "Hereditary xanthinuria type 1 (disorder)", "Deficiency of xanthine oxidase (disorder)", "Deficiency of xanthine oxidase (diagnosis)", "Isolated xanthine oxidase deficiency (disorder)", "disorders of purine and pyrimidine metabolism deficiency of xanthine oxidase"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "xanthinuria type I", "shortest_name_length": 4}
{"curie": "UMLS:C4525348", "names": ["0", "Stage 0 Intrahepatic Cholangiocarcinoma AJCC v8", "Stage 0 Intrahepatic Bile Duct Cancer (Cholangiocarcinoma)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Intrahepatic Cholangiocarcinoma AJCC v8", "shortest_name_length": 1}
{"curie": "UMLS:C1533592", "names": ["Malignant paraganglioma", "malignant paraganglioma", "Malignant Paraganglioma", "Metastatic Paraganglioma", "PARAGANGLIOMA, MALIGNANT", "Paraganglioma, malignant", "extra-adrenal paraganglioma", "Malignant Paraganglion Tumor", "Malignant Paraganglionic Tumor", "malignant tumor of paraganglia", "malignant paraganglia neoplasm", "Malignant Tumor of Paraganglion", "Paraganglion neoplasm malignant", "Malignant Paraganglion Neoplasm", "Malignant paraganglion neoplasm", "Paraganglion Neoplasm, Malignant", "Malignant Paraganglionic Neoplasm", "malignant neoplasm of paraganglia", "Malignant Neoplasm of Paraganglion", "malignant paraganglioma (diagnosis)", "Malignant Tumor of the Paraganglion", "Malignant Neoplasm of the Paraganglion", "Malignant neoplasm of paraganglion, NOS", "malignant neoplasm of paraganglia (diagnosis)", "Paraganglioma, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Paraganglionic Neoplasm", "shortest_name_length": 23}
{"curie": "UMLS:C1739104", "names": ["Acute graft versus host disease in liver"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute graft versus host disease in liver", "shortest_name_length": 40}
{"curie": "UMLS:C2721575", "names": ["Ischemic nephropathy", "Ischemic Nephropathy", "Ischaemic nephropathy", "nephropathy due to ischemia", "Nephropathy due to ischemia", "Nephropathy due to ischaemia", "Nephropathy due to ischemia (disorder)", "nephropathy due to ischemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ischemic nephropathy", "shortest_name_length": 20}
{"curie": "MONDO:0008705", "names": ["ACID PHOSPHATASE DEFICIENCY", "acid phosphatase deficiency", "Acid phosphatase deficiency", "Acid Phosphatase Deficiency", "acid phosphatase; deficiency", "deficiency; acid phosphatase", "Lysosomal acid phosphatase deficiency", "lysosomal acid phosphatase deficiency", "Acid phosphatase deficiency (disorder)", "ACID PHOSPHATASE, LYSOSOMAL, DEFICIENCY", "Lysosomal acid phosphatase deficiency syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lysosomal acid phosphatase deficiency", "shortest_name_length": 27}
{"curie": "MONDO:0017365", "names": ["congenital poikiloderma with bullae, Weary type", "hereditary acrokeratotic poikiloderma, Weary type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary acrokeratotic poikiloderma, Weary type", "shortest_name_length": 47}
{"curie": "MONDO:0013946", "names": ["HH15", "HS6ST1 hypogonadotropic hypogonadism", "HYPOGONADOTROPIC HYPOGONADISM 15 WITH OR WITHOUT ANOSMIA", "hypogonadotropic hypogonadism 15 with or without anosmia", "hypogonadotropic hypogonadism caused by mutation in HS6ST1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadotropic hypogonadism 15 with or without anosmia", "shortest_name_length": 4}
{"curie": "MONDO:0019205", "names": ["trichodysplasia-amelogenesis imperfecta syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichodysplasia-amelogenesis imperfecta syndrome", "shortest_name_length": 48}
{"curie": "MONDO:0060666", "names": ["HADDTS", "HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME", "hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C5418824", "names": ["Metastatic Desmoplastic Small Round Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Desmoplastic Small Round Cell Tumor", "shortest_name_length": 46}
{"curie": "UMLS:C0158371", "names": ["bone abscess", "abscess bone", "Osteomyelitis;acute", "Acute osteomyelitis", "osteomyelitis acute", "OSTEOMYELITIS ACUTE", "acute osteomyelitis", "Osteomyelitis acute", "acute; osteomyelitis", "osteomyelitis; acute", "Osteomyelitis acute NOS", "Acute osteomyelitis, NOS", "Acute osteomyelitis (disorder)", "acute osteomyelitis (diagnosis)", "Acute osteomyelitis, site unspecified", "Acute osteomyelitis with or without periostitis", "Acute or subacute osteomyelitis with or without mention of periostitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute osteomyelitis", "shortest_name_length": 12}
{"curie": "MONDO:0006532", "names": ["cholesteatoma; external ear", "external ear; cholesteatoma", "external canal cholesteatoma", "Cholesteatoma of external ear", "cholesteatoma of external ear", "external ear cholesteatoma (disease)", "cholesteatoma (disease) of external ear", "Cholesteatoma of external ear (disorder)", "cholesteatoma of external ear (diagnosis)", "Cholesteatoma of external ear, unspecified ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholesteatoma of external ear", "shortest_name_length": 27}
{"curie": "MONDO:0025377", "names": ["ASF", "Wart Hog Disease", "Wart-Hog Disease", "wart Hog disease", "wart-Hog disease", "Wart hog disease", "Wart-Hog Diseases", "wart-Hog diseases", "Asfivirus Infection", "African Swine Fever", "African swine fever", "Infection, Asfivirus", "swine fever, African", "Swine Fever, African", "Asfivirus Infections", "Infections, Asfivirus", "African swine fever (disorder)", "African Swine Fever Virus Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "African swine fever", "shortest_name_length": 3}
{"curie": "MONDO:0012399", "names": ["PMGYSA", "CDCBM7", "polymicrogyria due to TUBB2B mutation", "POLYMICROGYRIA, SYMMETRIC OR ASYMMETRIC", "polymicrogyria, symmetric or asymmetric", "complex cortical dysplasia with other brain malformations 7", "CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 7", "cortical dysplasia, Complex, with Other brain malformations 7", "cortical dysplasia, COMPLEX, with OTHER brain malformations 7", "TUBB2B complex cortical dysplasia with other brain malformations", "complex cortical dysplasia with other brain malformations type 7", "complex cortical dysplasia with other brain malformations caused by mutation in TUBB2B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complex cortical dysplasia with other brain malformations 7", "shortest_name_length": 6}
{"curie": "MONDO:0017380", "names": ["JIP", "JPS", "jPS", "PJI", "juvenile polyposis", "Juvenile Polyposis", "Juvenile Polyposis Coli", "JUVENILE POLYPOSIS COLI", "JUVENILE POLYPOSIS SYNDROME", "Juvenile polyposis syndrome", "Juvenile Polyposis Syndrome", "juvenile polyposis syndrome", "juvenile intestinal polyposis", "Juvenile Polyposis Of Infancy", "JUVENILE INTESTINAL POLYPOSIS", "JUVENILE POLYPOSIS, INFANTILE", "Juvenile intestinal polyposis", "polyposis juvenile intestinal", "JUVENILE POLYPOSIS OF STOMACH", "Juvenile Polyposis, Infantile", "JUVENILE POLYPOSIS OF INFANCY", "Juvenile Polyposis Of Stomach", "polyposis, juvenile intestinal", "POLYPOSIS, JUVENILE INTESTINAL", "Polyposis, juvenile intestinal", "Juvenile polyposis of intestine", "juvenile multiple polyps syndrome", "Juvenile Multiple Polyps Syndrome", "juvenile gastrointestinal polyposis", "Juvenile gastrointestinal polyposis", "Juvenile polyposis syndrome (disorder)", "polyposis familial of entire gastrointestinal tract", "POLYPOSIS, FAMILIAL, OF ENTIRE GASTROINTESTINAL TRACT", "Polyposis, familial, of entire gastrointestinal tract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile polyposis syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0007113", "names": ["AS", "ANCR", "puppet children", "Puppet Children", "Children, Puppet", "ANGELMAN SYNDROME", "angelman syndrome", "Angelman Syndrome", "syndrome angelman", "Angelman syndrome", "Syndrome, Angelman", "angelmans syndrome", "puppetlike syndrome", "Angelman's syndrome", "angelman's syndrome", "angelman's syndromes", "Happy puppet syndrome", "Happy Puppet Syndrome", "happy puppet syndrome", "Angelman syndrome (AS)", "Syndrome, Happy Puppet", "Angelman syndrome (Type 1)", "Angelman syndrome (Type 2)", "Angelman syndrome (disorder)", "Angelman syndrome (diagnosis)", "HAPPY PUPPET SYNDROME, FORMERLY", "happy puppet syndrome, formerly", "happy puppet syndrome (formerly)", "Happy puppet syndrome (formerly)", "Angelman syndrome chromosome region", "ANGELMAN SYNDROME CHROMOSOME REGION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Angelman syndrome", "shortest_name_length": 2}
{"curie": "MONDO:0037253", "names": ["ovary thecoma", "ovarian thecoma", "Ovarian thecoma", "Ovarian Thecoma", "Thecoma of Ovary", "Thecoma of ovary", "thecoma of ovary", "thecoma of the ovary", "Thecoma of the Ovary", "OVARY, THECA CELL TUMOR", "Ovarian Theca Cell Tumor", "Ovarian theca cell tumor", "ovarian theca cell tumor", "theca cell tumor of ovary", "Theca cell tumor of ovary", "Theca Cell Tumor of Ovary", "Ovarian theca cell tumour", "Theca cell tumour of ovary", "Ovarian Theca Cell Neoplasm", "ovarian theca cell neoplasm", "Theca Cell Neoplasm of Ovary", "theca cell neoplasm of ovary", "Theca Cell Tumor of the Ovary", "theca cell tumor of the ovary", "theca cell neoplasm of the ovary", "Theca Cell Neoplasm of the Ovary", "Theca cell tumor of ovary (disorder)", "theca cell tumor of ovary (diagnosis)", "malignant granulosa-theca cell tumor of ovary", "malignant granulosa-theca cell tumor of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian thecoma", "shortest_name_length": 13}
{"curie": "MONDO:0060622", "names": ["NEDMIAL", "NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE", "neurodevelopmental disorder with severe motor impairment and absent language"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with severe motor impairment and absent language", "shortest_name_length": 7}
{"curie": "MONDO:0003414", "names": ["Matrical carcinoma", "matrical carcinoma", "Matrical Carcinoma", "pilomatrix carcinoma", "Pilomatrix Carcinoma", "Pilomatrix carcinoma", "invasive pilomatrixoma", "Pilomatrical carcinoma", "Pilomatrical Carcinoma", "Invasive Pilomatrixoma", "malignant Pilomatricoma", "Malignant pilomatrixoma", "Malignant pilomatricoma", "malignant pilomatricoma", "Pilomatricoma, malignant", "Trichomatrical carcinoma", "pilomatricoma, malignant", "Pilomatrixoma, malignant", "pilomatrix skin carcinoma", "skin pilomatrix carcinoma", "Pilomatrix Skin Carcinoma", "Pilomatrix carcinoma of skin", "pilomatrix carcinoma of skin", "Pilomatrix Carcinoma of Skin", "Calcifying epitheliocarcinoma", "calcifying epitheliocarcinoma", "pilomatrix carcinoma of the skin", "Pilomatrix Carcinoma of the Skin", "Pilomatrix carcinoma of skin (disorder)", "pilomatrix carcinoma of skin (diagnosis)", "Calcified epithelial carcinoma of Malherbe", "calcified epithelial carcinoma of Malherbe", "Pilomatrix carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin pilomatrix carcinoma", "shortest_name_length": 18}
{"curie": "UMLS:C1334711", "names": ["Metastasizing Mixed Tumor of Salivary Gland", "Metastasizing Mixed Tumor of the Salivary Gland", "Metastasizing Pleomorphic Adenoma of the Salivary Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastasizing Pleomorphic Adenoma of the Salivary Gland", "shortest_name_length": 43}
{"curie": "UMLS:C0085622", "names": ["MONOPLEGIA", "Monoplegia", "monoplegia", "Monoplegias", "Monoplegia, NOS", "monoplegia was seen", "Monoplegia (disorder)", "Unspecified monoplegia", "Monoplegia, unspecified", "Paralysis of single limb", "monoplegia (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Monoplegia", "shortest_name_length": 10}
{"curie": "MONDO:0008083", "names": ["CLN4", "CLN4B", "CLN4B disease", "Kuf's disease type B", "autosomal dominant Kufs disease", "Autosomal Dominant Kufs Disease", "Kufs disease, autosomal dominant", "neuronal ceroid lipofuscinosis 4", "Kufs Disease, Autosomal Dominant", "neuronal ceroid lipofuscinosis 4B", "Kuf's disease, autosomal dominant", "Neuronal Ceroid Lipofuscinosis Type 4B", "neuronal ceroid lipofuscinosis type 4B", "adult neuronal ceroid lipofuscinosis 4B", "neuronal ceroid lipofuscinosis, parry type", "Neuronal Ceroid Lipofuscinosis, Parry Type", "Ceroid Lipofuscinosis, Neuronal, Parry Type", "ceroid lipofuscinosis, neuronal, parry type", "neuronal ceroid lipofuscinosis 4 Parry type", "CEROID LIPOFUSCINOSIS, NEURONAL, PARRY TYPE", "neuronal ceroid lipofuscinosis 4 parry type", "ceroid lipofuscinosis, neuronal, 4 (Kufs type)", "CEROID LIPOFUSCINOSIS, NEURONAL, 4 (KUFS TYPE)", "autosomal dominant neuronal ceroid lipofuscinosis 4B", "Ceroid Lipofuscinosis, Neuronal, 4B, Autosomal Dominant", "ceroid lipofuscinosis, neuronal, 4B, autosomal dominant", "ceroid lipofuscinosis, neuronal, 4 (Kufs type), autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ceroid lipofuscinosis, neuronal, 4 (Kufs type)", "shortest_name_length": 4}
{"curie": "UMLS:C5419206", "names": ["Advanced Esophageal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Esophageal Squamous Cell Carcinoma", "shortest_name_length": 43}
{"curie": "UMLS:C0267442", "names": ["gastroenteritis radiation", "Gastroenteritis radiation", "Radiation gastroenteritis", "radiation; gastroenteritis", "gastroenteritis; radiation", "gastroenteritis due to radiation", "Gastroenteritis due to radiation", "Radiation gastroenteritis (disorder)", "gastroenteritis due to radiation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radiation gastroenteritis", "shortest_name_length": 25}
{"curie": "UMLS:C0267516", "names": ["COLON ATONIC", "Colon atonic", "atonic colon", "Colonic atony", "colonic atony", "atony of colon", "Atony of colon", "Atony of colon (disorder)", "atony of colon (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atony of colon", "shortest_name_length": 12}
{"curie": "MONDO:0100288", "names": ["ESCS", "enhanced S-cone syndrome", "Enhanced S-Cone Syndrome", "ENHANCED S-CONE SYNDROME", "retinoschisis with early nyctalopia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "enhanced S-cone syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0002287", "names": ["glandular cystitis", "Cystitis Glandularis", "cystitis glandularis", "glandularis cystitis", "Cystitis glandularis", "Cystitis, glandularis", "Cystitis glandularis (disorder)", "glandularis cystitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glandular cystitis", "shortest_name_length": 18}
{"curie": "UMLS:C0223567", "names": ["L6 VERTEBRA", "L6 Vertebra", "Bone structure of L6", "Sixth lumbar vertebra", "sixth lumbar vertebra", "Extra Lumbar Vertebra", "Bone structure of L6 (body structure)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extra Lumbar Vertebra", "shortest_name_length": 11}
{"curie": "UMLS:C0520764", "names": ["Gastroenteritis clostridial", "gastroenteritis clostridial", "Clostridial gastroenteritis", "GASTROENTERITIS, CLOSTRIDIUM", "Clostridial gastroenteritis (disorder)", "Clostridial gastroenteritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clostridial gastroenteritis", "shortest_name_length": 27}
{"curie": "MONDO:0006793", "names": ["Hyperpituitarism", "hyperpituitarism", "HYPERPITUITARISM", "Hyperpituitarism NOS", "Hyperpituitarism, NOS", "Pituitary hyperfunction", "pituitary hyperfunction", "pituitary; hyperfunction", "hyperfunction; pituitary", "Hyperpituitarism (disorder)", "Pituitary hyperfunction, NOS", "Pituitary hyperfunction (ant.)", "anterior pituitary hyperfunction", "Anterior pituitary hyperfunction", "anterior pituitary hyperfunction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperpituitarism", "shortest_name_length": 16}
{"curie": "UMLS:C0751267", "names": ["Infantile Leigh Disease", "Leigh Disease, Infantile", "Infantile Subacute Necrotizing Encephalopathy", "Subacute Necrotizing Encephalopathy, Infantile", "Encephalopathy, Subacute Necrotizing, Infantile", "Subacute Necrotizing Encephalomyelitis, Infantile"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Encephalopathy, Subacute Necrotizing, Infantile", "shortest_name_length": 23}
{"curie": "MONDO:0010055", "names": ["Spinal Muscular Atrophy with Microcephaly and Mental Subnormality", "SPINAL MUSCULAR ATROPHY WITH MICROCEPHALY AND MENTAL SUBNORMALITY", "spinal muscular atrophy with microcephaly and mental subnormality"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal muscular atrophy with microcephaly and mental subnormality", "shortest_name_length": 65}
{"curie": "UMLS:C0920207", "names": ["Gastrointestinal Noninvasive Neoplasia", "Digestive System Intraepithelial Neoplasia", "Gastrointestinal Intraepithelial Neoplasia", "Gastrointestinal System Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal Intraepithelial Neoplasia", "shortest_name_length": 38}
{"curie": "MONDO:0004583", "names": ["transient retinal artery occlusion", "Transient retinal artery occlusion", "retina; occlusion artery, transient", "Transient arterial retinal occlusion", "occlusion; artery, retina, transient", "transient retinal arterial occlusion", "occlusion; retina, artery, transient", "Retinal transient arterial occlusion", "Transient Retinal Arterial Occlusion", "Transient retinal arterial occlusion", "transient arterial retinal occlusion", "retinal transient arterial occlusion", "obstruction; artery, retina, transient", "artery; retina, obstruction, transient", "transient retinal artery occlusion (diagnosis)", "Transient arterial retinal occlusion (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transient retinal arterial occlusion", "shortest_name_length": 34}
{"curie": "MONDO:0017748", "names": ["disorder of glycosphingolipid and GPI-anchored proteins glycosylation", "disorder of glycosphingolipid and glycosylphosphatidylinositol anchor glycosylation", "inborn disorder of glycosphingolipid and glycosylphosphatidylinositol anchor glycosylation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of glycosphingolipid and glycosylphosphatidylinositol anchor glycosylation", "shortest_name_length": 69}
{"curie": "UMLS:C1335711", "names": ["Relapsed Peripheral T-cell Lymphoma", "Recurrent Peripheral T-cell Lymphoma", "Recurrent Mature T- and NK-Cell Lymphoma", "Recurrent Mature T- and NK-Cell Non-Hodgkin's Lymphoma", "Recurrent Mature T-Cell and NK-Cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Mature T-Cell and NK-Cell Non-Hodgkin Lymphoma", "shortest_name_length": 35}
{"curie": "MONDO:0001586", "names": ["MPSI", "MPS1", "MPS I", "mps i", "MPS 1", "IDUA deficiency", "Hurler syndrome", "Lipochondrodystrophy", "lipochondrodystrophy", "Lipochondrodystrophies", "Hurler-Scheie syndrome", "mucopolysaccharidosis i", "MPS I - Hurler syndrome", "mucopolysaccharidosis I", "Mucopolysaccharidosis 1", "MUCOPOLYSACCHARIDOSIS I", "Mucopolysaccharidosis I", "i mucopolysaccharidosis", "Mucopolysaccharidosis Is", "L-iduronidase deficiency", "Hurler syndrome (subtype)", "mucopolysaccharidosis, MPS-I", "Mucopolysaccharidosis type I", "mucopolysaccharidosis type I", "mucopolysaccharidosis type 1", "Mucopolysaccharidosis, MPS-I", "Mucopolysaccharidosis type 1", "Mucopolysaccharidosis Type I", "mucopolysaccharidosis type i", "Mucopolysaccharidosis, type I", "mucopolysaccharidosis; type I", "type I; mucopolysaccharidosis", "mucopolysaccharidosis (MPS) I", "Mucopolysaccharidosis, type 1", "mucopolysaccharidosis, type 1", "iduronidase deficiency disease", "alpha-L-iduronidase deficiency", "Alpha-L-iduronidase deficiency", "lipochondrodystrophy (diagnosis)", "Hurler-Scheie syndrome (subtype)", "MPSI - Mucopolysaccharidosis type I", "mucopolysaccharide storage disease I", "Mucopolysaccharidosis, type I (MPS I)", "Mucopolysaccharidosis type I (disorder)", "mucopolysaccharidosis type 1 (diagnosis)", "alpha-L-iduronidase (IDA, IDUA) deficiency", "severe MPS I (subtype, also known as Hurler syndrome)", "attenuated MPS I (subtype, includes Hurler-Scheie and Scheie syndrome)", "Scheie syndrome (subtype) formerly known as Mucopoly-saccharidosis type V)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucopolysaccharidosis type 1", "shortest_name_length": 4}
{"curie": "MONDO:0043905", "names": ["pneumonias", "pulmonitis", "Pneumonitis", "pneumonitis", "PNEUMONITIS", "Pneumonitides", "Pneumonitis NOS", "inflammation lung", "Lung Inflammation", "Lung inflammation", "inflammation; lung", "lung; inflammation", "Lung Inflammations", "Inflammation, Lung", "Inflammations, Lung", "Pulmonary inflammation", "Pneumonitis (disorder)", "Pulmonary Inflammation", "pneumonitis (diagnosis)", "Inflammation, Pulmonary", "Pulmonary Inflammations", "Inflammations, Pulmonary", "lung parenchyma inflammation", "inflammation of lung parenchyma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pneumonitis", "shortest_name_length": 10}
{"curie": "MONDO:0011924", "names": ["PAND2", "Pand2", "panic disorder 2", "PANIC DISORDER 2", "panic disorder type 2", "panic disorder susceptibility locus, chromosome 9Q-related", "PANIC DISORDER SUSCEPTIBILITY LOCUS, CHROMOSOME 9q-RELATED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "panic disorder 2", "shortest_name_length": 5}
{"curie": "MONDO:0012258", "names": ["EBS2E", "EBS-migr", "EBS with circinate migratory erythema", "Epidermolysis bullosa simplex with circinate migratory erythema", "epidermolysis bullosa simplex with migratory circinate erythema", "Epidermolysis Bullosa Simplex with Migratory Circinate Erythema", "EPIDERMOLYSIS BULLOSA SIMPLEX WITH MIGRATORY CIRCINATE ERYTHEMA", "EPIDERMOLYSIS BULLOSA SIMPLEX 2E, WITH MIGRATORY CIRCINATE ERYTHEMA", "epidermolysis bullosa simplex 2E, with migratory circinate erythema", "Epidermolysis bullosa simplex with circinate migratory erythema (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolysis bullosa simplex 2E, with migratory circinate erythema", "shortest_name_length": 5}
{"curie": "UMLS:C0677705", "names": ["Stage II Mantle Cell Lymphoma", "noncontiguous stage II mantle cell lymphoma", "Stage II Non-Contiguous Mantle Cell Lymphoma", "Non-Contiguous Stage II Mantle Cell Lymphoma", "non-contiguous mantle cell lymphoma stage II", "Non-Contiguous Mantle Cell Lymphoma Stage II", "stage II non-contiguous mantle cell lymphoma", "Ann Arbor Stage II Non-Contiguous Mantle Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage II Non-Contiguous Mantle Cell Lymphoma", "shortest_name_length": 29}
{"curie": "MONDO:0006326", "names": ["extraocular extension melanoma", "extension, extrauveal melanoma", "Extraocular Extension Melanoma", "extraocular extension of melanoma", "Extraocular Extension of Melanoma", "intraocular melanoma extrauveal extension", "melanoma, intraocular extrauveal extension", "ocular melanoma with extraocular extension", "Ocular Melanoma with Extraocular Extension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ocular melanoma with extraocular extension", "shortest_name_length": 30}
{"curie": "UMLS:C0279920", "names": ["Pediatric LDHD", "Childhood LDHD", "HDLD, childhood", "LDHD, childhood", "LD HD, childhood", "HD LD, childhood", "lymphocyte depleted HD, childhood", "HD lymphocyte depleted, childhood", "childhood HD, lymphocyte depletion", "pediatric HD, lymphocyte depletion", "lymphocyte depletion HD, childhood", "Childhood Lymphocyte Depleted Hodgkin Lymphoma", "Lymphocyte Depleted Classical Hodgkin Lymphoma", "childhood lymphocyte depletion Hodgkin lymphoma", "pediatric lymphocyte depletion Hodgkin's disease", "Pediatric Lymphocyte Depletion Hodgkin's Disease", "Childhood Lymphocyte Depleted Hodgkin's Lymphoma", "childhood lymphocyte depletion Hodgkin's disease", "Pediatric Lymphocyte Depleted Hodgkin's Lymphoma", "childhood Hodgkin's disease, lymphocyte depleted", "Childhood Lymphocyte Depletion Hodgkin's Disease", "lymphocyte depleted Hodgkin's disease, childhood", "lymphocyte depletion Hodgkin's disease, childhood", "lymphoma, lymphocyte depleted childhood Hodgkin's", "Hodgkin's disease, lymphocyte depleted, childhood", "Pediatric Lymphocyte Depletion Hodgkin's Lymphoma", "pediatric Hodgkin's disease, lymphocyte depletion", "Childhood Lymphocyte Depletion Hodgkin's Lymphoma", "Childhood Lymphocyte-Depleted Classic Hodgkin Lymphoma", "Childhood Lymphocyte Depleted Classical Hodgkin Lymphoma", "Childhood Lymphocyte-Depleted Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Lymphocyte-Depleted Classic Hodgkin Lymphoma", "shortest_name_length": 14}
{"curie": "UMLS:C1510449", "names": ["Chronic Uveitis", "Chronic uveitis", "chronic uveitis", "Chronic Iridocyclitis", "iridocyclitis chronic", "chronic iridocyclitis", "Chronic iridocyclitis", "chronic; iridocyclitis", "iridocyclitis; chronic", "Chronic iridocyclitis, NOS", "chronic uveitis (diagnosis)", "chronic iridocyclitis (diagnosis)", "Chronic iridocyclitis, unspecified", "Chronic inflammation of uveal tract", "Chronic inflammation of uveal tract (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic iridocyclitis", "shortest_name_length": 15}
{"curie": "MONDO:0006869", "names": ["nodular goitre", "Goitre nodular", "Nodular goiter", "nodular goiter", "Goiter nodular", "GOITER NODULAR", "Nodular goitre", "Nodular Goiter", "nodular; goiter", "Nodular Goiters", "Goiter, nodular", "Goiter, Nodular", "struma; nodular", "nodular goiters", "goiter, nodular", "Goiters, Nodular", "Nodular goiter NOS", "Nodular Hyperplasia", "THYROID GOITER NODULAR", "nodular goiter (disease)", "Nodular goiter (disorder)", "Nodular goiter (diagnosis)", "Nodular hyperplasia of thyroid", "thyroid disorders goiter nodular"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nodular goiter", "shortest_name_length": 14}
{"curie": "MONDO:0016236", "names": ["KH", "KHE", "childhood Kaposi sarcoma", "Kaposiform Hemangioendothelioma", "Kaposiform hemangioendothelioma", "kaposiform hemangioendothelioma", "Kaposiform haemangioendothelioma", "Kaposiform hemangio-endothelioma", "Kaposiform hemangioendothelioma (disorder)", "Kaposiform hemangioendothelioma (diagnosis)", "Congenital cutaneous multifocal kaposiform hemangioendothelioma", "congenital cutaneous multifocal kaposiform hemangioendothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kaposiform hemangioendothelioma", "shortest_name_length": 2}
{"curie": "MONDO:0054770", "names": ["OFD18", "Ofds 18", "OFDS XVIII", "orofaciodigital syndrome 18", "orofaciodigital syndrome XVIII", "OROFACIODIGITAL SYNDROME XVIII", "Orofaciodigital syndrome type 18", "Oral-facial-digital syndrome type 18", "oral-Facial-digital syndrome, type 18", "ORAL-FACIAL-DIGITAL SYNDROME, TYPE XVIII", "OFD18 - oral-facial-digital syndrome type 18", "Oral-facial-digital syndrome with short stature and brachymesophalangy", "Oral-facial-digital syndrome with short stature and brachymesophalangia", "Oral-facial-digital syndrome with short stature and brachymesophalangia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orofaciodigital syndrome 18", "shortest_name_length": 5}
{"curie": "UMLS:C1332226", "names": ["Alcohol-Related Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alcohol-Related Carcinoma", "shortest_name_length": 25}
{"curie": "UMLS:C0232826", "names": ["antidiuresis", "Antidiuresis", "ANTIDIURESIS", "Anti-diuresis", "Anti-diuresis (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anti-diuresis (finding)", "shortest_name_length": 12}
{"curie": "MONDO:0012981", "names": ["HS4", "SPH4", "spherocytosis, type 4", "Spherocytosis, Type 4", "SPHEROCYTOSIS, TYPE 4", "hereditary spherocytosis 4", "spherocytosis, hereditary, 4", "Spherocytosis, Hereditary, 4", "SPHEROCYTOSIS, HEREDITARY, 4", "SLC4A1 hereditary spherocytosis", "hereditary spherocytosis type 4", "hereditary spherocytosis caused by mutation in SLC4A1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spherocytosis type 4", "shortest_name_length": 3}
{"curie": "UMLS:C1698769", "names": ["Urostomy Stenosis", "Urostomy stenosis", "Urostomy stenosis (diagnosis)", "postprocedural complications urostomy stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urostomy Stenosis", "shortest_name_length": 17}
{"curie": "MONDO:0030074", "names": ["SMDCD", "SMD-corneal dystrophy syndrome", "spondylometaphyseal dysplasia with corneal dystrophy", "SPONDYLOMETAPHYSEAL DYSPLASIA WITH CORNEAL DYSTROPHY", "Spondylometaphyseal dysplasia-corneal dystrophy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondylometaphyseal dysplasia with corneal dystrophy", "shortest_name_length": 5}
{"curie": "UMLS:C1336326", "names": ["Stage II Seminoma", "Stage II Seminoma of Testis", "Stage II Testicular Seminoma", "Stage II Seminoma of the Testis", "Stage II Testicular Seminoma AJCC v6", "Stage II Testicular Seminoma AJCC v7", "Stage II Testicular Seminoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Testicular Seminoma AJCC v6 and v7", "shortest_name_length": 17}
{"curie": "MONDO:0006286", "names": ["major salivary gland mucoepidermoid cancer", "Major Salivary Gland Mucoepidermoid Cancer", "Major Salivary Gland Mucoepidermoid Carcinoma", "major salivary gland mucoepidermoid carcinoma", "mucoepidermoid carcinoma of Major salivary gland", "Mucoepidermoid Carcinoma of Major Salivary Gland", "Mucoepidermoid Carcinoma of the Major Salivary Gland", "mucoepidermoid carcinoma of the Major salivary gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "major salivary gland mucoepidermoid carcinoma", "shortest_name_length": 42}
{"curie": "OMIM:612975", "names": ["FNSS1", "SHORT SLEEP PHENOTYPE", "SHORT SLEEP, FAMILIAL NATURAL, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 5}
{"curie": "UMLS:C4688416", "names": ["Stage I Uterine Corpus Adenosarcoma", "Stage I Uterine Corpus Adenosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Uterine Corpus Adenosarcoma AJCC v8", "shortest_name_length": 35}
{"curie": "MONDO:0011749", "names": ["OCA1B", "Oca1-Ts", "Amish albinism", "Yellow albinism", "YELLOW ALBINISM", "Xanthos albinism", "Xanthous albinism", "Yellow-type albinism", "Yellow mutant albinism", "albinism, Yellow mutant type", "Albinism, yellow mutant type", "Albinism, Yellow Mutant Type", "ALBINISM, YELLOW MUTANT TYPE", "Yellow oculocutaneous albinism", "Oculocutaneous albinism type 1B", "oculocutaneous albinism type 1B", "oculocutaneous albinism type IB", "oculocutaneous albinism type 1b", "platinum oculocutaneous albinism", "OCULOCUTANEOUS ALBINISM, TYPE IB", "Oculocutaneous Albinism, Type Ib", "oculocutaneous albinism, type 1B", "Platinum oculocutaneous albinism", "albinism, oculocutaneous, type IB", "albinism, oculocutaneous, type 1B", "ALBINISM, OCULOCUTANEOUS, TYPE IB", "Albinism, Oculocutaneous, Type Ib", "Oculocutaneous albinism, Amish type", "oculocutaneous albinism, Amish type", "Yellow mutant oculocutaneous albinism", "oculocutaneous albinism type 1b (diagnosis)", "Yellow mutant oculocutaneous albinism (disorder)", "albinism, oculocutaneous, type I, temperature-sensitive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculocutaneous albinism type 1B", "shortest_name_length": 5}
{"curie": "MONDO:0003927", "names": ["posterior uveal melanoma", "small size posterior uveal melanoma", "medium/large size posterior uveal melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "posterior uveal melanoma", "shortest_name_length": 24}
{"curie": "MONDO:0030936", "names": ["EPM12", "EPILEPSY, PROGRESSIVE MYOCLONIC, 12", "epilepsy, progressive myoclonic, 12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, progressive myoclonic, 12", "shortest_name_length": 5}
{"curie": "MONDO:0002738", "names": ["acute serous otitis media", "Acute middle ear effusion", "otitis media acute serous", "Acute secretory otitis media", "acute secretory otitis media", "otitis; media, effusion, acute", "otitis; media, secretory, acute", "acute transudative otitis media", "otitis; media, acute, secretory", "Acute transudative otitis media", "acute otitis media with effusion", "otitis media acute with effusion", "Acute otitis media with effusion", "otitis media acute nonsuppurative", "acute nonsuppurative otitis media", "Acute nonsuppurative otitis media", "Acute non-suppurative otitis media", "acute non-suppurative otitis media", "non-suppurative otitis media, acute", "otitis; media, acute, with effusion", "otitis; media, acute, nonsuppurative", "otitis; media, nonsuppurative, acute", "Acute MEE - Acute middle ear effusion", "Acute nonsuppurative otitis media, NOS", "Acute transudative otitis media (disorder)", "Acute otitis media with effusion (disorder)", "Acute otitis media with effusion (diagnosis)", "Acute non-suppurative otitis media (disorder)", "acute nonsuppurative otitis media (diagnosis)", "Acute nonsuppurative otitis media, unspecified", "Acute non-suppurative otitis media, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute transudative otitis media", "shortest_name_length": 25}
{"curie": "UMLS:C1336472", "names": ["Stage I Ovarian Embryonal Carcinoma", "Ovarian Embryonal Carcinoma, Stage I", "Stage I Ovarian Embryonal Carcinoma AJCC v6", "Stage I Ovarian Embryonal Carcinoma AJCC v7", "Stage I Ovarian Embryonal Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Ovarian Embryonal Carcinoma AJCC v6 and v7", "shortest_name_length": 35}
{"curie": "MONDO:0600009", "names": ["severe hypophosphatasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe hypophosphatasia", "shortest_name_length": 23}
{"curie": "MONDO:0010246", "names": ["EFMR", "DEE9", "EIEE9", "PCDH19-related FLE", "Juberg Hellman syndrome", "Juberg-Hellman syndrome", "JUBERG-HELLMAN SYNDROME", "PCDH19-related female-limited epilepsy", "early infantile epileptic encephalopathy 9", "Convulsive Disorder and Mental Retardation", "developmental and epileptic encephalopathy 9", "epileptic encephalopathy, early infantile, 9", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 9", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 9", "developmental and epileptic encephalopathy, 9", "PCDH19 early infantile epileptic encephalopathy", "early infantile epileptic encephalopathy type 9", "epileptic encephalopathy, early infantile, type 9", "PCDH19-related infantile epileptic encephalopathy", "epilepsy and mental retardation limited to females", "female restricted epilepsy with mental retardation", "female restricted epilepsy with intellectual deficit", "Epilepsy, Female-Restricted, with Mental Retardation", "epilepsy, female restricted, with mental retardation", "epilepsy, female-restricted, with mental retardation", "EPILEPSY, FEMALE-RESTRICTED, WITH MENTAL RETARDATION", "female restricted epilepsy with intellectual disability", "Female restricted epilepsy with intellectual disability", "epilepsy and intellectual disability limited to females", "early infantile female-limited epilecptic encephalopathy", "epilepsy, female restricted, with intellectual disability", "epilepsy, female-restricted, with intellectual disability", "familial epilepsy and mental retardation limited to females", "familial epilepsy and intellectual disability limited to females", "early infantile epileptic encephalopathy caused by mutation in PCDH19"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 9", "shortest_name_length": 4}
{"curie": "MONDO:0019648", "names": ["Achondrogenesis", "achondrogenesis", "Achondrogenesis, NOS", "Achondrogenesis Syndrome", "Achondrogenesis syndrome", "Achondrogenesis (disorder)", "Achondrogenesis (diagnosis)", "osteochondrodysplasia with defects of growth of tubular bones and spine achondrogenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "achondrogenesis", "shortest_name_length": 15}
{"curie": "UMLS:C5237350", "names": ["High-CSD Melanoma", "Cutaneous Melanoma with a High Degree of Cumulative Sun Damage", "Cutaneous Melanoma with a High Degree of Cumulative Sun Damage (CSD)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High-CSD Melanoma", "shortest_name_length": 17}
{"curie": "MONDO:0010965", "names": ["NSRD6", "DFNB6", "autosomal recessive deafness 6", "Deafness, Autosomal Recessive 6", "deafness, autosomal recessive 6", "DEAFNESS, AUTOSOMAL RECESSIVE 6", "deafness, autosomal recessive type 6", "autosomal recessive nonsyndromic deafness 6", "Neurosensory Nonsyndromic Recessive Deafness 6", "neurosensory nonsyndromic recessive deafness 6", "TMIE autosomal recessive nonsyndromic deafness", "NEUROSENSORY NONSYNDROMIC RECESSIVE DEAFNESS 6", "autosomal recessive nonsyndromic hearing loss 6", "autosomal recessive nonsyndromic deafness type 6", "autosomal recessive nonsyndromic deafness caused by mutation in TMIE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 6", "shortest_name_length": 5}
{"curie": "MONDO:0006894", "names": ["Patellofemoral syndrome", "patellofemoral syndrome", "Patellofemoral Syndrome", "patello femoral syndrome", "Patello femoral syndrome", "Anterior knee pain syndrome", "Anterior Knee Pain Syndrome", "pain patellofemoral syndrome", "Patellofemoral Pain Syndrome", "patellofemoral pain syndrome", "Patellofemoral pain syndrome", "Pain Syndrome, Patellofemoral", "Patellofemoral stress syndrome", "patellofemoral syndrome (diagnosis)", "Patellofemoral stress syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "patellofemoral pain syndrome", "shortest_name_length": 23}
{"curie": "UMLS:C0520775", "names": ["cystitis klebsiella", "Klebsiella cystitis", "Cystitis klebsiella", "Klebsiellal cystitis", "Klebsiella pneumoniae cystitis", "Klebsiella cystitis (disorder)", "Klebsiella cystitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Klebsiella cystitis", "shortest_name_length": 19}
{"curie": "UMLS:C0280351", "names": ["Stage II Mouth Mucoepidermoid Carcinoma", "Stage II Mucoepidermoid Carcinoma of Mouth", "Stage II Oral Cavity Mucoepidermoid Cancer", "Stage II Oral Cavity Mucoepidermoid Carcinoma", "oral cavity mucoepidermoid carcinoma, stage II", "Stage II Mucoepidermoid Carcinoma of the Mouth", "Stage II Mucoepidermoid Carcinoma of Oral Cavity", "stage II mucoepidermoid carcinoma of the oral cavity", "Stage II Mucoepidermoid Carcinoma of the Oral Cavity", "Mucoepidermoid carcinoma of the oral cavity stage II", "Stage II Oral Cavity Mucoepidermoid Carcinoma AJCC v7", "mucoepidermoid carcinoma of the oral cavity, stage II", "Stage II Oral Cavity Mucoepidermoid Carcinoma AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mucoepidermoid carcinoma of the oral cavity stage II", "shortest_name_length": 39}
{"curie": "MONDO:0006211", "names": ["fibrous hamartoma", "Fibrous Hamartoma", "Fibrous hamartoma", "Hamartoma, fibrous", "Infantile Fibrous Hamartoma", "infantile fibrous hamartoma", "fibrous hamartoma of infancy", "Fibrous hamartoma of infancy", "Fibrous Hamartoma of Infancy", "Fibrous hamartoma of infancy (disorder)", "Fibrous hamartoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibrous hamartoma of infancy", "shortest_name_length": 17}
{"curie": "UMLS:C4744524", "names": ["Fourth Ventricle Medulloblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fourth Ventricle Medulloblastoma", "shortest_name_length": 32}
{"curie": "MONDO:0012961", "names": ["T1D23", "IDDM23", "TYPE 1 DIABETES MELLITUS 23", "type 1 diabetes mellitus 23", "Insulin-Dependent Diabetes Mellitus 23", "insulin-dependent diabetes mellitus 23", "Diabetes Mellitus, Insulin-Dependent, 23", "diabetes mellitus, insulin-dependent, 23", "DIABETES MELLITUS, INSULIN-DEPENDENT, 23"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type 1 diabetes mellitus 23", "shortest_name_length": 5}
{"curie": "UMLS:C1332200", "names": ["Diffuse Astrocytoma", "WHO Grade 2 Astrocytoma", "WHO Grade II Astrocytoma", "Adult Diffuse Astrocytoma", "adult diffuse astrocytoma", "diffuse astrocytoma, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Diffuse Astrocytoma", "shortest_name_length": 19}
{"curie": "MONDO:0015312", "names": ["choanal atresia, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choanal atresia, unilateral", "shortest_name_length": 27}
{"curie": "MONDO:0001065", "names": ["shock obstetric syndrome", "Obstetric shock syndrome", "Supine hypotensive syndrome", "supine hypotensive syndrome", "syndrome; supine hypotensive", "supine hypotensive; syndrome", "maternal hypotension syndrome", "Maternal hypotension syndrome", "hypotension; maternal syndrome", "syndrome; maternal hypotension", "maternal; hypotension syndrome", "maternal; syndrome, hypotension", "Maternal hypotension syndrome (disorder)", "antepartum maternal hypotension syndrome", "postpartum maternal hypotension syndrome", "maternal hypotension syndrome (diagnosis)", "Maternal hypotension syndrome, unspecified trimester", "Maternal hypotension syndrome, unspecified as to episode of care or not applicable", "Maternal hypotension syndrome complicating labor and delivery, unspecified as to episode of care"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "supine hypotensive syndrome", "shortest_name_length": 24}
{"curie": "MONDO:0011662", "names": ["Gambling", "Gambling disorder", "addiction gambling", "Gambling addiction", "betting; addiction", "addiction; betting", "gambling addiction", "Compulsive Gambling", "Compulsive gambling", "addictions gambling", "compulsive gambling", "addiction; gambling", "gambling compulsive", "gambling; addiction", "pathologic; gambling", "gambling, pathologic", "gambling; dependence", "compulsion; gambling", "Gambling, Pathologic", "GAMBLING, PATHOLOGIC", "gambling; compulsion", "dependence; gambling", "pathological; betting", "Pathological gambling", "Gambling pathological", "betting; pathological", "Pathological Gambling", "gambling pathological", "pathological gambling", "gambling; pathological", "Gambling, Pathological", "Pathological Gamblings", "Gamblings, Pathological", "compulsive gambling disorder", "Pathological gambling disorder", "Compulsive gambling (disorder)", "pathological gambling (diagnosis)", "compulsive gambling disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pathological gambling", "shortest_name_length": 8}
{"curie": "MONDO:0019591", "names": ["Simmonds' disease", "Simmond's disease", "PANHYPOPITUITARISM", "Panhypopituitarism", "panhypopituitarism", "Panhypopituitarism, NOS", "primary hypopituitarism", "Primary hypopituitarism", "Complete Hypopituitarism", "complete hypopituitarism", "panhypopituitarism; syndrome", "syndrome; panhypopituitarism", "Panhypopituitarism (disorder)", "panhypopituitarism (diagnosis)", "combined pituitary hormone deficiency", "Combined Pituitary Hormone Deficiency", "Combined pituitary hormone deficiency", "Deficient secretion of all pituitary hormones"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "panhypopituitarism", "shortest_name_length": 17}
{"curie": "MONDO:0012299", "names": ["NNO2", "NANOPHTHALMOS 2", "Nanophthalmia 2", "NANOPHTHALMIA 2", "nanophthalmos 2", "Nanophthalmos 2", "MFRP nanophthalmia", "nanophthalmos type 2", "NANOPHTHALMOS 2 (disorder)", "NANOPHTHALMOS, AUTOSOMAL RECESSIVE", "nanophthalmos, autosomal recessive", "Nanophthalmos, Autosomal Recessive", "nanophthalmia caused by mutation in MFRP"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nanophthalmos 2", "shortest_name_length": 4}
{"curie": "UMLS:C1332901", "names": ["Cerebellar Glioneuronal and Neuronal Tumors", "Cerebellar Neuronal and Mixed Neuronal-Glial Tumor", "Neuronal and Mixed Neuronal-Glial Tumor of Cerebellum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebellar Glioneuronal and Neuronal Tumors", "shortest_name_length": 43}
{"curie": "MONDO:0017877", "names": ["Sabia hemorrhagic fever", "Sabia haemorrhagic fever", "Brazilian hemorrhagic fever", "Brazilian haemorrhagic fever", "Brazilian hemorrhagic fever (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brazilian hemorrhagic fever", "shortest_name_length": 23}
{"curie": "UMLS:C5557625", "names": ["Refractory T-Cell Large Granular Lymphocyte Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory T-Cell Large Granular Lymphocyte Leukemia", "shortest_name_length": 52}
{"curie": "UMLS:C3501849", "names": ["Mngie Without Leukoencephalopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mngie Without Leukoencephalopathy", "shortest_name_length": 33}
{"curie": "UMLS:C2609072", "names": ["Cleft Jaw", "Gnathoschisis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gnathoschisis", "shortest_name_length": 9}
{"curie": "MONDO:0014665", "names": ["CMT2V", "NAGLU Charcot-Marie-Tooth disease", "Charcot-Marie-Tooth neuropathy type 2V", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2V", "Charcot-Marie-Tooth neuropathy, type 2V", "Charcot-Marie-Tooth disease axonal type 2V", "Charcot-Marie-Tooth disease, axonal, type 2V", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2V", "hereditary adult-onset painful axonal polyneuropathy", "Hereditary adult onset painful axonal polyneuropathy", "Hereditary adult-onset painful axonal polyneuropathy", "Autosomal dominant Charcot-Marie-Tooth disease type 2V", "autosomal dominant Charcot-Marie-Tooth disease type 2V", "Charcot-Marie-Tooth disease caused by mutation in NAGLU", "autosomal dominant axonal Charcot-Marie-Tooth disease type 2V", "Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2V", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2V", "Autosomal dominant Charcot-Marie-Tooth disease type 2V (disorder)", "Autosomal dominant Charcot-Marie-Tooth disease type 2 due to NAGLU mutation", "autosomal dominant Charcot-Marie-Tooth disease type 2 due to NAGLU mutation", "Autosomal dominant Charcot-Marie-Tooth disease type 2 due to NAGLU (N-acetyl-alpha-glucosaminidase) mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease axonal type 2V", "shortest_name_length": 5}
{"curie": "MONDO:0010163", "names": ["TYROSINOSIS", "tyrosinosis", "Tyrosinosis", "Tyrosinosis, NOS", "Tyrosinosis (disorder)", "tyrosinosis (diagnosis)", "Excessive accumulation of tyrosine in tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tyrosinosis", "shortest_name_length": 11}
{"curie": "MONDO:0007557", "names": ["EBD, Bart type", "epidermolysis bullosa dystrophica, Bart type", "Epidermolysis Bullosa Dystrophica, Bart Type", "EPIDERMOLYSIS BULLOSA DYSTROPHICA, BART TYPE", "Epidermolysis bullosa dystrophica, Bart type", "Dominant dystrophic epidermolysis bullosa with absence of skin", "Dominant dystrophic epidermolysis bullosa with absence of skin (disorder)", "EPIDERMOLYSIS BULLOSA WITH CONGENITAL LOCALIZED ABSENCE OF SKIN AND DEFORMITY OF NAILS", "Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails", "epidermolysis bullosa with congenital localized absence of skin and deformity of nails"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolysis bullosa with congenital localized absence of skin and deformity of nails", "shortest_name_length": 14}
{"curie": "UMLS:C1334792", "names": ["Moderately Differentiated Prostate Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Moderately Differentiated Prostate Adenocarcinoma", "shortest_name_length": 49}
{"curie": "MONDO:0020783", "names": ["PKWS", "CMAVM1", "Parkes-Weber syndrome", "Parkes Weber syndrome", "parkes weber syndrome", "Parkes Weber syndrome (disorder)", "Capillary Malformation-Arteriovenous Malformation", "CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION 1", "capillary malformation-arteriovenous malformation 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "capillary malformation-arteriovenous malformation 1", "shortest_name_length": 4}
{"curie": "UMLS:C1516066", "names": ["Astler-Coller B3 Colorectal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Astler-Coller B3 Colorectal Carcinoma", "shortest_name_length": 37}
{"curie": "UMLS:C0278844", "names": ["childhood IBL lymphoma", "Immunoblastic Lymphoma", "pediatric IBL lymphoma", "IBL lymphoma, childhood", "Pediatric Immunoblastic Lymphoma", "Childhood Immunoblastic Lymphoma", "Childhood Immunoblastic Large Cell Lymphoma", "Pediatric Immunoblastic Large Cell Lymphoma", "childhood immunoblastic large cell lymphoma", "pediatric immunoblastic large cell lymphoma", "immunoblastic large cell lymphoma, childhood", "lymphoma, immunoblastic large cell childhood", "large cell lymphoma, childhood immunoblastic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Immunoblastic Lymphoma", "shortest_name_length": 22}
{"curie": "MONDO:0003993", "names": ["Vaginal Childhood Sarcoma Botryoides", "vaginal childhood sarcoma Botryoides", "Childhood Sarcoma Botryoides of the Vagina", "childhood sarcoma Botryoides of the vagina", "childhood vagina botryoid rhabdomyosarcoma", "Childhood Vaginal Embryonal Rhabdomyosarcoma", "vaginal childhood botryoid-type embryonal rhabdomyosarcoma", "Vaginal Childhood Botryoid-Type Embryonal Rhabdomyosarcoma", "Childhood Vaginal Botryoid-Type Embryonal Rhabdomyosarcoma", "childhood botryoid-type embryonal rhabdomyosarcoma of the vagina", "pediatric botryoid-type embryonal rhabdomyosarcoma of the vagina", "Childhood Botryoid-Type Embryonal Rhabdomyosarcoma of the Vagina", "botryoid-type embryonal rhabdomyosarcoma of the vagina of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood vagina botryoid rhabdomyosarcoma", "shortest_name_length": 36}
{"curie": "UMLS:C5206670", "names": ["Penile Rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Penile Rhabdomyosarcoma", "shortest_name_length": 23}
{"curie": "MONDO:0004786", "names": ["Chronic Cholangitis", "Chronic cholangitis", "Cholangitis chronic", "chronic cholangitis", "cholangitis, chronic", "Cholangitis chronic NOS", "Chronic cholangitis NOS", "Chronic cholangitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic cholangitis", "shortest_name_length": 19}
{"curie": "MONDO:0016523", "names": ["Bronchial cyst", "Bronchial Cyst", "bronchial cyst", "Cyst, Bronchial", "Bronchial Cysts", "Single lung cyst", "Cysts, Bronchial", "Bronchogenic cyst", "Bronchogenic Cyst", "bronchogenic cyst", "Cyst, bronchogenic", "bronchogenic cysts", "Bronchogenic Cysts", "Cyst, Bronchogenic", "cyst; bronchogenic", "bronchogenic; cyst", "Cysts, Bronchogenic", "Congenital bronchial cyst", "bronchogenic cyst (disease)", "Congenital bronchogenic cyst", "cyst; bronchogenic, congenital", "bronchogenic; cyst, congenital", "Congenital bronchogenic cyst (disorder)", "Bronchogenic cyst (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bronchogenic cyst", "shortest_name_length": 14}
{"curie": "UMLS:C5555517", "names": ["Leaky SCID", "Leaky Severe Combined Immunodeficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leaky Severe Combined Immunodeficiency", "shortest_name_length": 10}
{"curie": "UMLS:C2981670", "names": ["Stage IA Ampulla of Vater Cancer", "Stage IA Ampulla of Vater Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Ampulla of Vater Cancer AJCC v7", "shortest_name_length": 32}
{"curie": "MONDO:0017612", "names": ["JEB", "EBJ", "junctional epidermolysis bullosa", "Junctional epidermolysis bullosa", "epidermolysis bullosa junctional", "Junctional Epidermolysis Bullosa", "epidermolysis bullosa atrophicans", "epidermolysis bullosa, junctional", "Epidermolysis Bullosa, Junctional", "Epidermolysis bullosa atrophicans", "Junctional epidermolysis bullosa, NOS", "epidermolysis bullosa hereditaria letalis", "Congenital junctional epidermolysis bullosa", "Junctional epidermolysis bullosa (disorder)", "congenital junctional epidermolysis bullosa", "Junctional epidermolysis bullosa (diagnosis)", "EPIDERMOLYSIS BULLOSA JUNCTIONALIS, DISENTIS TYPE", "Epidermolysis Bullosa Junctionalis, Disentis Type", "Epidermolysis Bullosa, Generalized Atrophic Benign", "Epidermolysis Bullosa Junctionalis, Severe Nonlethal", "EPIDERMOLYSIS BULLOSA JUNCTIONALIS, SEVERE NONLETHAL", "Congenital junctional epidermolysis bullosa (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "junctional epidermolysis bullosa", "shortest_name_length": 3}
{"curie": "UMLS:C0080032", "names": ["malignant effusion", "effusion malignant", "Malignant effusion", "Malignant pleural effusion", "pleural effusion malignant", "effusion pleural malignant", "PLEURAL EFFUSION MALIGNANT", "Malignant Pleural Effusion", "effusion malignant pleural", "malignant pleural effusion", "effusion; pleura, malignant", "malignant pleural effusions", "Pleural Effusion, Malignant", "Malignant Pleural Effusions", "Effusion, Malignant Pleural", "pleural effusion, malignant", "Neoplastic pleural effusion", "pleura; effusion, malignant", "Effusions, Malignant Pleural", "Pleural Effusions, Malignant", "malignant pleural effusion (diagnosis)", "Pleural effusion due to neoplastic disease", "Pleural effusion due to neoplastic disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pleural Effusion, Malignant", "shortest_name_length": 18}
{"curie": "MONDO:0008078", "names": ["Fsnf", "FSNF", "Familial spinal neurofibromatosis", "NEUROFIBROMATOSIS, FAMILIAL SPINAL", "neurofibromatosis, familial spinal", "Neurofibromatosis, Familial Spinal", "Familial spinal neurofibromatosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurofibromatosis, familial spinal", "shortest_name_length": 4}
{"curie": "MONDO:0013666", "names": ["STL5", "STICKLER SYNDROME, TYPE V", "Stickler syndrome, type 5", "STICKLER syndrome, type V", "COL9A2 autosomal recessive Stickler syndrome", "autosomal recessive Stickler syndrome caused by mutation in COL9A2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stickler syndrome, type 5", "shortest_name_length": 4}
{"curie": "MONDO:0006844", "names": ["Magnesium Deficiency", "deficiency magnesium", "Magnesium deficiency", "magnesium deficiency", "deficiency; magnesium", "Deficiency, Magnesium", "magnesium; deficiency", "Magnesium Deficiencies", "magnesium deficiencies", "Deficiencies, Magnesium", "Magnesium deficiency (disorder)", "magnesium deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "magnesium deficiency", "shortest_name_length": 20}
{"curie": "UMLS:C4527329", "names": ["Refractory Central Nervous System Lymphoma", "Refractory Primary Central Nervous System Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Central Nervous System Lymphoma", "shortest_name_length": 42}
{"curie": "MONDO:0001038", "names": ["PERFORATED CORNEAL ULCER", "ULCER CORNEAL PERFORATED", "Perforated corneal ulcer", "perforated corneal ulcer", "Ulcer corneal perforated", "Perforated corneal ulcer (disorder)", "perforated corneal ulcer (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "perforated corneal ulcer", "shortest_name_length": 24}
{"curie": "MONDO:0023563", "names": ["Kotzot-Richter syndrome", "albinism with immune and hematologic defects", "Albinism with immune and hematologic defects", "Oculocutaneous albinism, immunodeficiency, hematological disorders, and minor anomalies", "oculocutaneous albinism, immunodeficiency, hematological disorders, and minor anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kotzot-Richter syndrome", "shortest_name_length": 23}
{"curie": "UMLS:C1334233", "names": ["Intestinal Precancerous Condition", "Intestinal Premalignant Condition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal Precancerous Condition", "shortest_name_length": 33}
{"curie": "MONDO:0006028", "names": ["cecum adenocarcinoma", "cecal adenocarcinoma", "Cecal Adenocarcinoma", "Cecal adenocarcinoma", "Cecum Adenocarcinoma", "caecum adenocarcinoma", "Adenocarcinoma of cecum", "adenocarcinoma of cecum", "Adenocarcinoma of Cecum", "Adenocarcinoma of caecum", "adenocarcinoma of the cecum", "Adenocarcinoma of the Cecum", "Adenocarcinoma of cecum (disorder)", "adenocarcinoma of cecum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cecum adenocarcinoma", "shortest_name_length": 20}
{"curie": "MONDO:0012539", "names": ["JBTS6", "Joubert syndrome 6", "JOUBERT SYNDROME 6", "TMEM67 Joubert syndrome", "Joubert syndrome type 6", "Joubert syndrome caused by mutation in TMEM67"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome 6", "shortest_name_length": 5}
{"curie": "MONDO:0015283", "names": ["maternally-inherited cardiomyopathy and deafness", "maternally-inherited cardiomyopathy and hearing loss", "tRNA-LYS-related cardiomyopathy-hearing loss syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maternally-inherited cardiomyopathy and hearing loss", "shortest_name_length": 48}
{"curie": "MONDO:0012383", "names": ["NKCD", "IMD54", "NKGCD", "IMMUNODEFICIENCY 54", "Immunodeficiency 54", "immunodeficiency 54", "mini-chromosome maintenance 4", "Mini-chromosome Maintenance 4", "Primary immunodeficiency due to MCM4 deficiency", "primary immunodeficiency due to MCM4 deficiency", "familial isolated natural killer cell deficiency", "NATURAL KILLER CELL DEFICIENCY, FAMILIAL ISOLATED", "Natural Killer Cell Deficiency, Familial Isolated", "natural Killer cell deficiency, familial isolated", "natural KILLER cell and glucocorticoid deficiency with DNA repair defect", "Natural Killer Cell and Glucocorticoid Deficiency with DNA Repair Defect", "NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT", "Primary immunodeficiency with natural killer cell deficiency and adrenal insufficiency", "Primary immunodeficiency with natural-killer cell deficiency and adrenal insufficiency", "primary immunodeficiency with natural-killer cell deficiency and adrenal insufficiency", "Primary immunodeficiency due to MCM4 (mini-chromosome maintenance complex component 4) deficiency", "Primary immunodeficiency with natural killer cell deficiency and adrenal insufficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary immunodeficiency with natural-killer cell deficiency and adrenal insufficiency", "shortest_name_length": 4}
{"curie": "MONDO:0001877", "names": ["infertility due to extratesticular cause", "Infertility due to extratesticular cause", "Infertility due to extratesticular causes", "infertility due to extratesticular causes", "Infertility due to extratesticular cause (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infertility due to extratesticular cause", "shortest_name_length": 40}
{"curie": "MONDO:0019650", "names": ["steroid-sensitive MCNS", "idiopathic steroid-sensitive nephrotic syndrome with minimal change"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic steroid-sensitive nephrotic syndrome with minimal change", "shortest_name_length": 22}
{"curie": "MONDO:0032732", "names": ["DFNB113", "autosomal recessive deafness 113", "DEAFNESS, AUTOSOMAL RECESSIVE 113", "deafness, autosomal recessive 113", "hearing loss, autosomal recessive 113", "autosomal recessive nonsyndromic deafness 113"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal recessive 113", "shortest_name_length": 7}
{"curie": "UMLS:C4285731", "names": ["Leptomeningeal Myelomatosis", "Leptomeningeal myelomatosis", "Leptomeningeal Plasma Cell Myeloma", "Extramedullary Disease in Multiple Myeloma Involving the Leptomeninges", "Extramedullary Disease in Plasma Cell Myeloma Involving the Leptomeninges"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leptomeningeal myelomatosis", "shortest_name_length": 27}
{"curie": "MONDO:0003939", "names": ["muscular disease", "muscular disorder", "muscle organ disease", "muscle tissue disease", "muscle tissue disorder", "disease of muscle organ", "disorder of muscle organ", "disease of muscle tissue", "disorder of muscle tissue", "muscle organ disease or disorder", "muscle tissue disease or disorder", "disease or disorder of muscle organ", "disease or disorder of muscle tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscle tissue disorder", "shortest_name_length": 16}
{"curie": "MONDO:0018462", "names": ["Angelman syndrome due to imprinting defect in 15q11-q13"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Angelman syndrome due to imprinting defect in 15q11-q13", "shortest_name_length": 55}
{"curie": "EFO:0000266", "names": ["aortic stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic stenosis", "shortest_name_length": 15}
{"curie": "UMLS:C1328409", "names": ["Propofol syndrome", "Propofol Syndrome", "Propofol Syndromes", "Propofol Infusion Syndrome", "Propofol infusion syndrome", "Propofol Infusion Syndromes", "Propofol-Related Infusion Syndrome", "Propofol Related Infusion Syndrome", "Propofol-Related Infusion Syndromes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Propofol Infusion Syndrome", "shortest_name_length": 17}
{"curie": "MONDO:0014447", "names": ["BBS19", "Bardet-Biedl syndrome 19", "BARDET-BIEDL SYNDROME 19", "IFT27 Bardet-Biedl syndrome", "Bardet-Biedl syndrome type 19", "Bardet-Biedl syndrome caused by mutation in IFT27"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bardet-Biedl syndrome 19", "shortest_name_length": 5}
{"curie": "MONDO:0044308", "names": ["BBS21", "Bardet-Biedl syndrome 21", "bardet-biedl syndrome 21", "BARDET-BIEDL SYNDROME 21"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bardet-biedl syndrome 21", "shortest_name_length": 5}
{"curie": "MONDO:0003565", "names": ["urethra villous adenoma", "Urethral Villous Adenoma", "urethral villous adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urethral villous adenoma", "shortest_name_length": 23}
{"curie": "UMLS:C3272265", "names": ["THREE VESSEL DISEASE", "Three Vessel Coronary Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Three Vessel Coronary Disease", "shortest_name_length": 20}
{"curie": "UMLS:C1879677", "names": ["Alcohol Toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alcohol Toxicity", "shortest_name_length": 16}
{"curie": "MONDO:0000487", "names": ["Hemidystonia", "hemidystonia", "Hemidystonia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemidystonia", "shortest_name_length": 12}
{"curie": "UMLS:C0278473", "names": ["stage IV adult HD", "adult HD, stage IV", "HD, adult, stage IV", "HD, stage IV, adult", "adult HD, metastatic", "HD, adult, metastatic", "HD, metastatic, adult", "Stage IV Hodgkin Lymphoma", "Stage IV Adult Hodgkin Lymphoma", "stage IV adult Hodgkin lymphoma", "Stage IV Adult Hodgkin's Disease", "stage IV adult Hodgkin's disease", "Adult Hodgkin's Disease Stage IV", "Stage IV Adult Hodgkin's Lymphoma", "adult Hodgkin's disease, stage IV", "Adult Hodgkin's Lymphoma Stage IV", "metastatic adult Hodgkin's disease", "lymphoma, stage IV adult Hodgkin's", "Hodgkin's disease, stage IV, adult", "Hodgkin's lymphoma, stage IV, adult", "Metastatic Adult Hodgkin's Lymphoma", "adult Hodgkin's disease, metastatic", "lymphoma, metastatic adult Hodgkin's", "Hodgkin's disease, metastatic, adult", "Hodgkin's lymphoma, metastatic, adult", "Ann Arbor Stage IV Adult Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Adult Hodgkin Lymphoma", "shortest_name_length": 17}
{"curie": "MONDO:0018897", "names": ["primary cutaneous CD30+ T-cell lymphoproliferative disease", "primary cutaneous Ki-1+ T-cell lymphoproliferative disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary cutaneous CD30+ T-cell lymphoproliferative disease", "shortest_name_length": 58}
{"curie": "MONDO:0005832", "names": ["LYMPHANGITIS", "Lymphangitis", "lymphangitis", "Lymphangitides", "Lymphangitis NOS", "Lymphangitis, NOS", "inflammation lymphatic", "Lymphangitis (disorder)", "lymphangitis (diagnosis)", "Inflammation of lymphatics", "lymphatic vessel inflammation", "lymphatic vessel; inflammation", "inflammation; lymphatic vessel", "inflammation of lymphatic vessel"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphangitis", "shortest_name_length": 12}
{"curie": "MONDO:0020179", "names": ["EYELID NEVUS", "eyelid nevus", "Eyelid Nevus", "Eyelid nevus", "Eyelid naevus", "Nevus of eyelid", "nevus of eyelid", "palpebral nevus", "Nevus of Eyelid", "Naevus of eyelid", "nevus of the eyelid", "Nevus of the Eyelid", "Nevus of eyelid (disorder)", "skin of eyelid melanocytic nevus", "melanocytic nevus of skin of eyelid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "palpebral nevus", "shortest_name_length": 12}
{"curie": "MONDO:0021534", "names": ["Rectal NET G1", "rectal NET G1", "rectum NET G1", "Rectal Carcinoid", "rectal carcinoid", "Carcinoid of Rectum", "carcinoid of rectum", "Rectal Carcinoid Tumor", "rectum carcinoid tumor", "rectal carcinoid tumor", "carcinoid of the rectum", "Carcinoid of the Rectum", "Carcinoid tumor of rectum", "Carcinoid Tumor of Rectum", "carcinoid tumor of rectum", "Carcinoid tumour of rectum", "carcinoid tumor of the rectum", "Carcinoid tumor in the rectum", "Carcinoid Tumor of the Rectum", "rectal neuroendocrine tumor G1", "Rectal Neuroendocrine Tumor G1", "Carcinoid tumour in the rectum", "rectum carcinoid tumor (disease)", "rectum neuroendocrine neoplasm G1", "Carcinoid tumor of rectum (disorder)", "grade 1 neuroendocrine neoplasm of rectum", "rectum neuroendocrine tumor, well differentiated, low grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rectal neuroendocrine tumor G1", "shortest_name_length": 13}
{"curie": "UMLS:C4525728", "names": ["Cortical Cataract Grade 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cortical Cataract Grade 2", "shortest_name_length": 25}
{"curie": "UMLS:C0281197", "names": ["skin changes due to radiation therapy", "radiation therapy, secondary skin reactions", "Skin Reaction Secondary to Radiation Therapy", "skin reactions secondary to radiation therapy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin Reaction Secondary to Radiation Therapy", "shortest_name_length": 37}
{"curie": "MONDO:0009927", "names": ["3MC2", "OSA SYNDROME", "Osa syndrome", "3MC syndrome 2", "3MC SYNDROME 2", "Carnevale syndrome", "3MC syndrome type 2", "3Mc syndrome type 2", "COLEC11 3MC syndrome", "CARNEVALE SYNDROME, FORMERLY", "Carnevale syndrome, formerly", "oculo-skeletal-abdominal syndrome", "OCULO-SKELETAL-ABDOMINAL SYNDROME", "Oculo-skeletal-abdominal syndrome", "Carnevale Krajewska Fischetto syndrome", "3MC syndrome caused by mutation in COLEC11", "Ptosis of eyelids with diastasis recti and hip dysplasia", "PTOSIS OF EYELIDS WITH DIASTASIS RECTI AND HIP DYSPLASIA", "ptosis of eyelids-diastasis recti-hip dysplasia syndrome", "ptosis of eyelids with diastasis recti and hip dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "3MC syndrome 2", "shortest_name_length": 4}
{"curie": "UMLS:C1336766", "names": ["Tonsillar Lymphoepithelioma", "Tonsillar Undifferentiated Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tonsillar Undifferentiated Carcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C5554728", "names": ["Relapsed B Acute Lymphoblastic Leukemia with t(9;22)(q34.1;q11.2); BCR-ABL1", "Recurrent B Acute Lymphoblastic Leukemia with t(9;22)(q34.1;q11.2); BCR-ABL1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent B Acute Lymphoblastic Leukemia with t(9;22)(q34.1;q11.2); BCR-ABL1", "shortest_name_length": 75}
{"curie": "UMLS:C0342856", "names": ["COPROPORPHYRIA", "Coproporphyria", "coproporphyria", "Porphyria hepatica II", "Coproporphyria (disorder)", "coproporphyria (diagnosis)", "Porphyria Hepatica, Coproporphyria", "Hereditary coproporphyria porphyria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Coproporphyria", "shortest_name_length": 14}
{"curie": "UMLS:C1516059", "names": ["Astler-Coller B1 Colon Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Astler-Coller B1 Colon Carcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C1334592", "names": ["Malignant Intracranial Germ Cell Tumor", "Malignant Intracranial Germ Cell Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Intracranial Germ Cell Tumor", "shortest_name_length": 38}
{"curie": "MONDO:0019225", "names": ["gluconeogenesis disorder", "disorder of gluconeogenesis", "inborn error of gluconeogenesis", "inborn gluconeogenesis disorder", "rare inborn error of gluconeogenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of gluconeogenesis", "shortest_name_length": 24}
{"curie": "UMLS:C5421319", "names": ["Endometrial Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endometrial Neuroendocrine Carcinoma", "shortest_name_length": 36}
{"curie": "UMLS:C4725027", "names": ["Refractory Acute Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Acute Leukemia", "shortest_name_length": 25}
{"curie": "MONDO:0005299", "names": ["Brain Ischemia", "brain ischemia", "Brain ischemia", "ischemia brain", "brain; ischemic", "Ischemia, Brain", "ischemia; brain", "Brain Ischemias", "cerebral ischemia", "Cerebral Ischemia", "Ischemia cerebral", "ISCHEMIA CEREBRAL", "ischemia cerebral", "CEREBRAL ISCHEMIA", "Cerebral ischemia", "Ischaemia cerebral", "Cerebral ischaemia", "cerebral ischaemia", "CEREBRAL ISCHAEMIA", "ischemia; cerebral", "cerebral; ischemic", "Cerebral Ischemias", "Ischemia, Cerebral", "Ischaemia;cerebral", "Ischemias, Cerebral", "Cerebral ischemia, NOS", "brain ischemic disease", "Cerebral ischaemia, NOS", "Ischemic Encephalopathy", "encephalopathy ischemic", "ischemic encephalopathy", "Ischemic encephalopathy", "Encephalopathy, Ischemic", "ischaemic encephalopathy", "Ischemia cerebrovascular", "Cerebrovascular Ischemia", "ischemia cerebrovascular", "Ischaemic encephalopathy", "cerebrovascular ischemia", "ISCHEMIA CEREBROVASCULAR", "Cerebrovascular ischemia", "cerebrovascular ischaemia", "ischemic disease of brain", "Ischaemia cerebrovascular", "Ischemic Encephalopathies", "cerebrovascular; ischemic", "Cerebral ischemia (disorder)", "cerebral ischemia (diagnosis)", "CEREBRAL VASCULAR INSUFFICIENCY", "Ischemic encephalopathy (disorder)", "Cerebrovascular insufficiency syndrome", "Disruption of blood oxygen supply to brain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brain ischemia", "shortest_name_length": 14}
{"curie": "MONDO:0014957", "names": ["LADCI", "language delay and ADHD/cognitive impairment with or without cardiac arrhythmia", "LANGUAGE DELAY AND ATTENTION DEFICIT-HYPERACTIVITY DISORDER/COGNITIVE IMPAIRMENT WITH OR WITHOUT CARDIAC ARRHYTHMIA", "language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia", "language delay and attention Deficit-hyperactivity disorder/cognitive impairment with or without Cardiac arrhythmia", "language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia; LADCI"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia", "shortest_name_length": 5}
{"curie": "MONDO:0015044", "names": ["MU HCD", "mu-HCD", "mu Chain Disease", "MU CHAIN DISEASE", "mu-Chain Disease", "mu chain disease", "mu-Chain Diseases", "mu heavy chain disease", "Mu Heavy Chain Disease", "mu-heavy chain disease", "MU HEAVY-CHAIN DISEASE", "Mu-heavy chain disease", "heavy chain disease mu", "MU HEAVY CHAIN DISEASE", "Mu heavy chain disease", "IGM HEAVY CHAIN DISEASE", "IgM heavy chain disease", "Heavy chain disease, IgM type", "Mu heavy chain disease (disorder)", "Mu heavy chain disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mu-heavy chain disease", "shortest_name_length": 6}
{"curie": "MONDO:0012114", "names": ["Ehlers-Danlos syndrome, Beasley-Cohen type", "Ehlers-Danlos Syndrome, Beasley-Cohen Type", "Ehlers-Danlos syndrome, Beasley Cohen type", "EHLERS-DANLOS SYNDROME, BEASLEY-COHEN TYPE", "Ehlers-Danlos syndrome with mental retardation, deafness, and cataract", "EHLERS-DANLOS SYNDROME WITH MENTAL RETARDATION, DEAFNESS, AND CATARACT", "Ehlers-Danlos syndrome with intellectual disability, deafness, and cataract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ehlers-Danlos syndrome, Beasley-Cohen type", "shortest_name_length": 42}
{"curie": "MONDO:0054581", "names": ["TBS1", "rear syndrome", "Townes-Brocks syndrome 1", "TOWNES-BROCKS SYNDROME 1", "renal-ear-anal-radial syndrome", "townes-brocks branchiootorenal-like syndrome", "TOWNES-BROCKS-BRANCHIOOTORENAL-LIKE SYNDROME", "Townes-Brocks-Branchiootorenal-Like Syndrome", "Townes-Brocks-branchiootorenal-like syndrome", "anus, imperforate, with hand, Foot, and Ear anomalies", "deafness, sensorineural, with imperforate anus and thumb anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Townes-Brocks syndrome 1", "shortest_name_length": 4}
{"curie": "UMLS:C5206719", "names": ["Advanced Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Breast Carcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0001260", "names": ["lake Itch", "Lake Itch", "Duck Itch", "duck Itch", "Swamp itch", "swimmer itch", "SWIMMER ITCH", "itch swimmers", "Sea lice rash", "swimmer's itch", "Swimmers' itch", "itch swimmer's", "Swimmer's itch", "Swimmer's Itch", "swimmers' itch", "itch; swimmer's", "CLAM DIGGER ITCH", "Marine dermatitis", "Clam-digger's itch", "Clam digger's itch", "clam digger's; itch", "itch; clam digger's", "cercarial dermatitis", "Cercarial dermatitis", "Cercarial Dermatitis", "Sea bather's eruption", "cercarial; dermatitis", "dermatitis; cercarial", "sea bather's eruption", "Schistosome dermatitis", "Schistosoma; cercariae", "SCHISTOSOME DERMATITIS", "cutaneous schistosomiasis", "Schistosomiasis cutaneous", "Cutaneous Schistosomiasis", "Cutaneous schistosomiasis", "SCHISTOSOMIASIS, CUTANEOUS", "schistosomiasis; cutaneous", "cutaneous; schistosomiasis", "Sea bather's eruption (disorder)", "Schistosomal cercarial dermatitis", "Cutaneous schistosomiasis (disorder)", "Infection by cercariae of Schistosoma", "Infection by cercariae of schistosoma", "schistosomiasis; Schistosoma cercariae", "schistosomiasis dermatitis (swimmer's itch)", "schistosomiasis dermatitis (swimmer's itch) (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cercarial dermatitis", "shortest_name_length": 9}
{"curie": "UMLS:C1334211", "names": ["Skin Intermediate Fibrohistiocytic Neoplasm", "Intermediate Cutaneous Fibrohistiocytic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin Intermediate Fibrohistiocytic Neoplasm", "shortest_name_length": 43}
{"curie": "MONDO:0005182", "names": ["serous cystadenofibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "serous cystadenofibroma", "shortest_name_length": 23}
{"curie": "UMLS:C4055195", "names": ["Congenital TSH Deficiency", "Congenital Isolated TSH Deficiency", "Congenital Isolated Thyroid Stimulating Hormone Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Isolated Thyroid Stimulating Hormone Deficiency", "shortest_name_length": 25}
{"curie": "MONDO:0019656", "names": ["sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis", "shortest_name_length": 89}
{"curie": "UMLS:C4725091", "names": ["Metastatic Uveal Melanoma", "metastatic uveal melanoma", "uveal melanoma, metastatic", "melanoma, uveal metastatic", "metastatic intraocular melanoma", "intraocular melanoma, metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Uveal Melanoma", "shortest_name_length": 25}
{"curie": "MONDO:0006004", "names": ["Vasomotor Rhinitis", "RHINITIS VASOMOTOR", "Rhinitis;vasomotor", "Vasomotor rhinitis", "vasomotor rhinitis", "VASOMOTOR RHINITIS", "vasomotor; rhinitis", "Rhinitis, Vasomotor", "rhinitis; vasomotor", "Vasomotor Rhinitides", "Rhinitides, Vasomotor", "Vasomotor rhinitis, NOS", "VMR - Vasomotor rhinitis", "Vasomotor rhinitis (disorder)", "vasomotor rhinitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vasomotor rhinitis", "shortest_name_length": 18}
{"curie": "MONDO:0001956", "names": ["CLS", "SCLS", "AVLS", "Capillary leak", "Clarkson disease", "Clarkson Disease", "Capillary leak syndrome", "CAPILLARY LEAK SYNDROME", "capillary leak syndrome", "Capillary Leak Syndrome", "Capillary Leak Syndromes", "capillary leaking syndrome", "acute vascular leak syndrome", "Acute vascular leak syndrome", "Acute Vascular Leak Syndrome", "Systemic Capillary Leak Syndrome", "systemic capillary leak syndrome", "Increased capillary permeability", "Systemic capillary leak syndrome", "idiopathic capillary leak syndrome", "Idiopathic capillary leak syndrome", "Capillary leak syndrome (disorder)", "capillary leak syndrome (diagnosis)", "Capillary hyperpermeability syndrome", "capillary hyperpermeability syndrome", "periodic systemic capillary leak syndrome", "Increased capillary permeability (finding)", "capillary leak syndrome with monoclonal gammopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "capillary leak syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C0750949", "names": ["Vertebral hyperesthesia", "Vertebrogenic Pain Syndrome", "Vertebrogenic pain syndrome", "Syndrome, Vertebrogenic Pain", "Pain Syndrome, Vertebrogenic", "Vertebrogenic Pain Syndromes", "Syndromes, Vertebrogenic Pain", "Pain Syndromes, Vertebrogenic", "Vertebrogenic pain syndrome, NOS", "Vertebrogenic (pain) syndrome NOS", "Vertebrogenic pain syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vertebrogenic Pain Syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0004727", "names": ["oral opening cancer", "cancer of oral opening", "vestibule of mouth cancer", "malignant oral opening neoplasm", "malignant neoplasm of oral opening", "Malignant tumor of vestibule of mouth", "malignant tumor of vestibule of mouth", "Malignant tumour of vestibule of mouth", "Malignant neoplasm of vestibule of mouth", "malignant neoplasm of vestibule of mouth", "Malignant tumor of vestibule of mouth (disorder)", "oral cavity neoplasm malignant vestibule of mouth", "malignant neoplasm of vestibule of mouth (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vestibule of mouth cancer", "shortest_name_length": 19}
{"curie": "UMLS:C4329666", "names": ["Chronic Myelomonocytic Leukemia with Eosinophilia Associated with t(5;12)", "Chronic Myelomonocytic Leukemia with Eosinophilia Associated with t(5;12)(q31;p12)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic Myelomonocytic Leukemia with Eosinophilia Associated with t(5;12)(q31;p12)", "shortest_name_length": 73}
{"curie": "UMLS:C4687715", "names": ["Progressive Medulloblastoma, SHH-Activated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Progressive Medulloblastoma, SHH-Activated", "shortest_name_length": 42}
{"curie": "MONDO:0020447", "names": ["coronary sinus atresia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coronary sinus atresia", "shortest_name_length": 22}
{"curie": "MONDO:0000659", "names": ["delta chain disease", "IgD heavy chain disease", "delta heavy chain disease", "Delta heavy chain disease", "delta-heavy chain disease", "heavy chain disease delta", "Heavy chain disease, IgD type", "Delta heavy chain disease (disorder)", "Delta heavy chain disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "delta-heavy chain disease", "shortest_name_length": 19}
{"curie": "UMLS:C1112459", "names": ["Unresectable Hepatocellular Cancer", "Liver cell carcinoma non-resectable", "Unresectable Hepatocellular Carcinoma", "Hepatocellular carcinoma non-resectable", "Non-Resectable Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Hepatocellular Carcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0033643", "names": ["IBD30", "inflammatory bowel disease 30", "INFLAMMATORY BOWEL DISEASE (CROHN DISEASE) 30", "inflammatory bowel disease (Crohn disease) 30"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory bowel disease 30", "shortest_name_length": 5}
{"curie": "MONDO:0054802", "names": ["ECYT7", "erythrocytosis 7", "familial erythrocytosis 7", "ERYTHROCYTOSIS, FAMILIAL, 7", "erythrocytosis, familial, 7", "erythrocytosis, FAMILIAL, 7", "alpha-globin type polycythemia", "POLYCYTHEMIA, ALPHA-GLOBIN TYPE", "polycythemia, Alpha-globin type", "alpha-globin type erythrocytosis", "ERYTHROCYTOSIS, ALPHA-GLOBIN TYPE", "erythrocytosis, Alpha-globin type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythrocytosis, familial, 7", "shortest_name_length": 5}
{"curie": "UMLS:C1541263", "names": ["Stage I Marginal Zone Lymphoma", "Marginal zone lymphoma stage I", "stage I marginal zone lymphoma", "stage I marginal zone B-cell lymphoma", "Stage I Marginal Zone B-Cell Lymphoma", "Ann Arbor Stage I Marginal Zone Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Marginal zone lymphoma stage I", "shortest_name_length": 30}
{"curie": "MONDO:0008927", "names": ["ODRMD", "MCOPCT2", "Microphthalmia and Cataract 2", "Microphthalmia, Cataract, and Nystagmus", "Microphthalmia, Isolated, with Cataract 2", "optic DISC anomalies with retinal and/or macular dystrophy", "OPTIC DISC ANOMALIES WITH RETINAL AND/OR MACULAR DYSTROPHY", "optic disc anomalies with retinal and/or macular dystrophy", "Colobomatous optic disc-macular atrophy-chorioretinopathy syndrome", "colobomatous optic disc-macular atrophy-chorioretinopathy syndrome", "Colobomatous optic disc, macular atrophy, chorioretinopathy syndrome", "Colobomatous optic disc, macular atrophy, chorioretinopathy syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colobomatous optic disc-macular atrophy-chorioretinopathy syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0281773", "names": ["acute glaucoma", "Acute glaucoma", "Acute Glaucoma", "glaucoma; acute", "acute; glaucoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute glaucoma", "shortest_name_length": 14}
{"curie": "UMLS:C4528664", "names": ["Stage II Appendix Cancer", "Stage II Appendix Carcinoma AJCC v8", "Stage II Appendiceal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Appendix Carcinoma AJCC v8", "shortest_name_length": 24}
{"curie": "UMLS:C0862201", "names": ["Recurrent Sezary Syndrome", "Sezary syndrome recurrent", "Sezary's disease recurrent", "Sezary's syndrome recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sezary syndrome recurrent", "shortest_name_length": 25}
{"curie": "UMLS:C4763787", "names": ["Recurrent Plasmablastic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Plasmablastic Lymphoma", "shortest_name_length": 32}
{"curie": "MONDO:0032785", "names": ["PAPA10", "polydactyly, postaxial, type a10", "POLYDACTYLY, POSTAXIAL, TYPE A10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polydactyly, postaxial, type a10", "shortest_name_length": 6}
{"curie": "UMLS:C0948824", "names": ["ANEMIA BLOOD LOSS", "blood loss anemia", "Blood loss anemia", "hemorrhagic anemia", "blood loss anaemia", "Anaemia;blood loss", "anemia hemorrhagic", "blood loss; anemia", "hemorrhage; anemia", "anemia; hemorrhage", "anemia; blood loss", "Hemorrhagic anemia", "Blood loss anaemia", "anemia; hemorrhagic", "hemorrhagic; anemia", "Haemorrhagic anaemia", "haemorrhagic anaemia", "anemia blood due loss", "Anemia due to blood loss", "anemia due to blood loss", "anemia; due to blood loss", "Anaemia due to blood loss", "anemia secondary to blood loss", "Anemia due to blood loss (disorder)", "anemia secondary to blood loss (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anemia due to blood loss", "shortest_name_length": 17}
{"curie": "MONDO:0008036", "names": ["myasthenia gravis, limb-girdle", "Myasthenia Gravis, Limb-Girdle", "MYASTHENIA GRAVIS, LIMB-GIRDLE", "MYASTHENIA, LIMB-GIRDLE, AUTOIMMUNE", "Myasthenia, Limb-Girdle, Autoimmune", "myasthenia, limb-girdle, autoimmune"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myasthenia, limb-girdle, autoimmune", "shortest_name_length": 30}
{"curie": "MONDO:0018028", "names": ["5p tetrasomy", "tetrasomy 5p", "Tetrasomy 5p", "Isochromosome 5p", "tetrasomy type 5p", "Tetrasomy 5p syndrome", "chromosome 5p tetrasomy syndrome", "Tetrasomy 5p syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tetrasomy 5p", "shortest_name_length": 12}
{"curie": "MONDO:0018003", "names": ["limbic encephalitis with DPPX antibodies", "limbic encephalitis with DPP6 antibodies", "limbic encephalitis with dipeptidyl-peptidase 6 antibodies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "limbic encephalitis with DPP6 antibodies", "shortest_name_length": 40}
{"curie": "MONDO:0100111", "names": ["FSGSNEDS", "FOCAL SEGMENTAL GLOMERULOSCLEROSIS AND NEURODEVELOPMENTAL SYNDROME", "focal segmental glomerulosclerosis and neurodevelopmental syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal segmental glomerulosclerosis and neurodevelopmental syndrome", "shortest_name_length": 8}
{"curie": "UMLS:C0677957", "names": ["Stage III Non-Hodgkin Lymphoma", "Stage III Non-Hodgkin's Lymphoma", "Non-Hodgkin's Lymphoma Stage III", "Non-Hodgkin's lymphoma stage III", "Non-Hodgkin's lymphoma NOS stage III", "Ann Arbor Stage III Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Non-Hodgkin Lymphoma", "shortest_name_length": 30}
{"curie": "UMLS:C0525041", "names": ["Cognitive Symptom", "Cognitive Symptoms", "cognitive symptoms", "Symptom, Cognitive", "Symptoms, Cognitive", "Cognitive Manifestation", "Manifestation, Cognitive", "Cognitive Manifestations", "Manifestations, Cognitive", "Neurobehavioral Manifestation", "Manifestation, Neurobehavioral", "Neurobehavioral Manifestations", "Manifestations, Neurobehavioral", "Neurobehavioral Signs and Symptoms", "Signs and Symptoms, Neurobehavioral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neurobehavioral Manifestations", "shortest_name_length": 17}
{"curie": "MONDO:0030915", "names": ["MRT61", "ALWADEI SYNDROME", "Alwadei syndrome", "autosomal recessive mental retardation 61", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 61", "mental retardation, autosomal recessive 61", "autosomal recessive intellectual disability 61", "intellectual disability, autosomal recessive 61", "autosomal recessive intellectual developmental disorder-61", "autosomal recessive intellectual developmental disorder 61", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 61"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 61", "shortest_name_length": 5}
{"curie": "UMLS:C0281706", "names": ["Stage IV Burkitt Lymphoma", "Stage IV Childhood Burkitt Lymphoma", "Stage IV Childhood Burkitt's Lymphoma", "Ann Arbor Stage IV Childhood Burkitt Lymphoma", "stage IV childhood small noncleaved cell lymphoma", "lymphoma, stage IV childhood small noncleaved cell", "Stage IV Childhood Small Non-Cleaved Cell Lymphoma", "Stage IV Pediatric Small Non-Cleaved Cell Lymphoma", "Childhood Small Non-Cleaved Cell Lymphoma Stage IV", "pediatric small noncleaved cell lymphoma, stage IV", "childhood small noncleaved cell lymphoma, stage IV", "Pediatric Small Non-Cleaved Cell Lymphoma Stage IV", "metastatic childhood small noncleaved cell lymphoma", "small noncleaved cell lymphoma, childhood, stage IV", "lymphoma, metastatic childhood small noncleaved cell", "Metastatic Pediatric Small Non-Cleaved Cell Lymphoma", "childhood small noncleaved cell lymphoma, metastatic", "Metastatic Childhood Small Non-Cleaved Cell Lymphoma", "pediatric small noncleaved cell lymphoma, metastatic", "small noncleaved cell lymphoma, childhood, metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Childhood Burkitt Lymphoma", "shortest_name_length": 25}
{"curie": "MONDO:0005525", "names": ["t cell leukemia", "T-cell leukemia", "leukemia t cell", "T Cell Leukemia", "t-cell leukemia", "T-Cell Leukemia", "leukemia t-cell", "cells leukemia t", "Leukemia, T Cell", "T-Cell Leukemias", "Leukemia, T-Cell", "Leukemias, T-Cell", "T-Lymphocytic Leukemia", "T Lymphocytic Leukemia", "Leukemia, T Lymphocytic", "Leukemia, T-Lymphocytic", "T-Lymphocytic Leukemias", "Lymphocytic Leukemia, T", "T Lymphocytic Leukemias", "Leukemias, T-Lymphocytic", "Lymphocytic Leukemias, T", "Leukemias, T Lymphocytic", "T cell leukemia (disease)", "T-cell lymphocytic leukemia", "t-cell lymphocytic leukemia", "T-Cell Lymphocytic Leukemia", "Lymphocytic Leukemia, T Cell", "leukemia (disease) of T cell", "Lymphocytic Leukemia, T-Cell", "Leukemia, T-Cell Lymphocytic", "T-Cell Lymphocytic Leukemias", "Lymphocytic Leukemias, T-Cell", "Leukemia, Lymphocytic, T Cell", "Leukemia, Lymphocytic, T-Cell", "Leukemias, T-Cell Lymphocytic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-cell leukemia", "shortest_name_length": 15}
{"curie": "UMLS:C4552921", "names": ["IA2", "Stage IA2 Cervical Cancer", "Stage IA2 Cervical Cancer AJCC v8", "Stage IA2 Cervical Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA2 Cervical Cancer AJCC v8", "shortest_name_length": 3}
{"curie": "MONDO:0032584", "names": ["ECTN14", "ECTD14", "ectodermal dysplasia 14", "ectodermal dysplasia 14, hair/tooth type with or without hypohidrosis", "ECTODERMAL DYSPLASIA 14, HAIR/TOOTH TYPE WITH OR WITHOUT HYPOHIDROSIS", "ECTODERMAL DYSPLASIA 14, HAIR/TOOTH TYPE, WITH OR WITHOUT HYPOHIDROSIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia 14, hair/tooth type with or without hypohidrosis", "shortest_name_length": 6}
{"curie": "UMLS:C1336389", "names": ["Stage IVB Paranasal Sinus Cancer", "Stage IVB Accessory Sinus Carcinoma", "Stage IVB Paranasal Sinus Carcinoma", "Stage IVB Carcinoma of Accessory Sinus", "Stage IVB Carcinoma of Paranasal Sinus", "Stage IVB Paranasal Sinus Cancer AJCC v7", "Stage IVB Carcinoma of the Paranasal Sinus", "Stage IVB Carcinoma of the Accessory Sinus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Paranasal Sinus Cancer AJCC v7", "shortest_name_length": 32}
{"curie": "MONDO:0044406", "names": ["Stoll-Alembik-Finck syndrome", "arthrogryposis-ectodermal dysplasia-other anomalies syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis-ectodermal dysplasia-other anomalies syndrome", "shortest_name_length": 28}
{"curie": "UMLS:C4525586", "names": ["Stage II Gastric Neuroendocrine Tumor", "Stage II Gastric Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Gastric Neuroendocrine Tumor AJCC v8", "shortest_name_length": 37}
{"curie": "UMLS:C0275761", "names": ["Pneumococcal pharyngitis", "Pharyngitis, pneumococcal", "pharyngitis; pneumococcal", "pneumococcal; pharyngitis", "Pneumococcal pharyngitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pneumococcal pharyngitis", "shortest_name_length": 24}
{"curie": "MONDO:0006196", "names": ["Uterine Serous Carcinoma", "uterine serous carcinoma", "papillary carcinoma of uterus", "uterine serous adenocarcinoma", "Uterine Serous Adenocarcinoma", "papillary carcinoma of the uterus", "endometrial serous adenocarcinoma", "serous endometrial adenocarcinoma", "Serous endometrial adenocarcinoma", "Endometrial Serous Adenocarcinoma", "carcinoma, papillary, endometrial", "carcinoma of the uterus, papillary", "uterus cancer, papillary carcinoma", "uterine papillary serous carcinoma", "Uterine Papillary Serous Carcinoma", "uterine cancer, papillary carcinoma", "uterine corpus serous adenocarcinoma", "Uterine Corpus Serous Adenocarcinoma", "endometrial papillary serous carcinoma", "Papillary serous endometrial carcinoma", "uterine serous papillary adenocarcinoma", "Uterine Serous Papillary Adenocarcinoma", "papillary carcinoma of uterus (diagnosis)", "uterine corpus cancer, papillary carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometrial serous adenocarcinoma", "shortest_name_length": 24}
{"curie": "MONDO:0015515", "names": ["CPT2", "CPTII", "CPT-II", "Cpt2 Deficiency", "CPT II Deficiency", "CPT II deficiency", "Cpt Ii Deficiency", "Carnitine palmitoyltransferase 2 deficiency", "Carnitine Palmitoyltransferase 2 Deficiency", "Carnitine Palmitoyltransferase II Deficiency", "Carnitine palmitoyltransferase II deficiency", "Carnitine Palmitoyltransferase Ii Deficiency", "carnitine palmitoyltransferase II deficiency", "Carnitine palmitoyl transferase 2 deficiency", "Carnitine palmitoyltransferase deficiency type 2", "Carnitine palmitoyltransferase type II deficiency", "CPT2 - Carnitine palmitoyltransferase II deficiency", "Carnitine palmitoyltransferase II (CPT II) deficiency", "infantile carnitine palmitoyltransferase II deficiency", "Carnitine palmitoyltransferase II deficiency (disorder)", "late-onset carnitine palmitoyltransferase II deficiency", "Muscle form of carnitine palmitoyltransferase deficiency", "CPTII - Carnitine palmitoyltransferase deficiency type II", "lethal neonatal carnitine palmitoyltransferase II deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carnitine palmitoyltransferase II deficiency", "shortest_name_length": 4}
{"curie": "UMLS:C0877424", "names": ["cytomegalovirus infection systemic", "Disseminated cytomegalovirus infection", "CYTOMEGALOVIRUS INFECTION DISSEMINATED", "Disseminated cytomegaloviral infection", "Disseminated cytomegalovirus infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disseminated cytomegalovirus infection", "shortest_name_length": 34}
{"curie": "UMLS:C5669816", "names": ["Myeloid Neoplasms with Germline SAMD9 Mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myeloid Neoplasms with Germline SAMD9 Mutation", "shortest_name_length": 46}
{"curie": "UMLS:C2987477", "names": ["Stage II Vulvar Cancer", "Stage II Vulvar Carcinoma", "Stage II Vulvar Cancer AJCC v7", "Stage II Vulvar Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Vulvar Cancer AJCC v7", "shortest_name_length": 22}
{"curie": "UMLS:C5418576", "names": ["Skin Spindle Cell/Pleomorphic Lipoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin Spindle Cell/Pleomorphic Lipoma", "shortest_name_length": 36}
{"curie": "MONDO:0004535", "names": ["Childhood Ovarian Choriocarcinoma", "pediatric ovarian choriocarcinoma", "childhood ovarian choriocarcinoma", "Pediatric Ovarian Choriocarcinoma", "pediatric choriocarcinoma of ovary", "Pediatric Choriocarcinoma of Ovary", "childhood choriocarcinoma of ovary", "pediatric Choriocarcinoma of Ovary", "Childhood Choriocarcinoma of Ovary", "choriocarcinoma of ovary of childhood", "pediatric choriocarcinoma of the ovary", "childhood choriocarcinoma of the ovary", "Pediatric Choriocarcinoma of the Ovary", "Childhood Choriocarcinoma of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood choriocarcinoma of the ovary", "shortest_name_length": 33}
{"curie": "MONDO:0020818", "names": ["DENTIN SECOND", "SECOND DENTIN", "tertiary dentine", "irregular dentin", "Irregular dentin", "secondary dentin", "Secondary Dentin", "Tertiary dentine", "Secondary dentin", "secondary; dentin", "dentin; irregular", "irregular dentine", "secondary dentine", "Secondary dentine", "Dentin, Secondary", "irregular; dentin", "Irregular dentine", "sclerotic dentine", "Sclerotic dentine", "dentin; secondary", "Secondary Dentins", "Reparative dentine", "reparative dentine", "Dentins, Secondary", "Secondary dentin (disorder)", "secondary dentin (diagnosis)", "secondary dentin formation in the pulp", "secondary dentin formation in pulp of tooth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary dentine", "shortest_name_length": 13}
{"curie": "MONDO:0011059", "names": ["Genoa syndrome", "GENOA SYNDROME", "Camera Lituania Cohen syndrome", "Camero Lituania Cohen syndrome", "camera Lituania Cohen syndrome", "Camero-Lituania-Cohen syndrome", "Holoprosencephaly craniosynostosis", "holoprosencephaly craniosynostosis", "Holoprosencephaly craniosynostosis syndrome", "holoprosencephaly-craniosynostosis syndrome", "Holoprosencephaly-craniosynostosis syndrome", "holoprosencephaly, SEMILOBAR, with craniosynostosis", "Holoprosencephaly, Semilobar, With Craniosynostosis", "HOLOPROSENCEPHALY, SEMILOBAR, WITH CRANIOSYNOSTOSIS", "Holoprosencephaly craniosynostosis syndrome (disorder)", "Semilobar holoprosencephaly and primary craniosynostosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "holoprosencephaly-craniosynostosis syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0010716", "names": ["pterygium syndrome multiple X-linked", "multiple pterygium syndrome X-linked", "multiple pterygium syndrome, X-linked", "Multiple Pterygium Syndrome, X-Linked", "MULTIPLE PTERYGIUM SYNDROME, X-LINKED", "pterygium syndrome, multiple, X-linked", "Pterygium Syndrome, Multiple, X-Linked", "PTERYGIUM SYNDROME, MULTIPLE, X-LINKED", "X-linked lethal multiple pterygium syndrome", "lethal multiple pterygium syndrome, X-linked", "X-linked lethal multiple pterygium syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked lethal multiple pterygium syndrome", "shortest_name_length": 36}
{"curie": "MONDO:0002824", "names": ["extrinsic cardiomyopathy", "Secondary cardiomyopathy", "secondary cardiomyopathy", "Cardiomyopathy, secondary", "Cardiomyopathy associated with another disorder", "Cardiomyopathy in other diseases classified elsewhere", "Cardiomyopathy associated with another disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extrinsic cardiomyopathy", "shortest_name_length": 24}
{"curie": "MONDO:0018075", "names": ["NTD", "NTDS", "Spinal Dysraphism", "spinal dysraphism", "Neural tube defect", "neural tube defect", "defect neural tube", "NEURAL TUBE DEFECT", "Neural Tube Defect", "Defect, Neural Tube", "Neural Tube Defects", "neural tube defects", "defects neural tube", "Neural tube defects", "tube neural defects", "Defects, Neural Tube", "NTD - Neural tube defect", "Neural tube defect (disorder)", "Neural tube defect (diagnosis)", "Neural Tube Developmental Defects", "Developmental Neural Tube Defects", "Abnormality of neural tube closure", "Developmental Defects, Neural Tube"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neural tube defect", "shortest_name_length": 3}
{"curie": "MONDO:0044200", "names": ["T-B+ SCID", "T-cell negative B-cell positive SCID", "T-B+ severe combined immunodeficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-B+ severe combined immunodeficiency", "shortest_name_length": 9}
{"curie": "MONDO:0015505", "names": ["tracheal anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tracheal anomaly", "shortest_name_length": 16}
{"curie": "MONDO:0011052", "names": ["ACLH", "Yim Ebbin syndrome", "BRACHIAL AMELIA, CLEFT LIP, AND HOLOPROSENCEPHALY", "brachial AMELIA, cleft LIP, and holoprosencephaly", "amelia cleft lip palate hydrocephalus iris coloboma", "brachial amelia, forebrain defects and facial clefts", "Brachial amelia, forebrain defects and facial clefts", "Brachial Amelia, Forebrain Defects, and Facial Clefts", "brachial amelia, forebrain defects, and Facial clefts", "BRACHIAL AMELIA, FOREBRAIN DEFECTS, AND FACIAL CLEFTS", "Amelia, cleft lip, palate, hydrocephalus, iris coloboma", "bilateral brachial amelia, facial clefts, encephalocele, orbital cyst and omphalocele"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amelia cleft lip palate hydrocephalus iris coloboma", "shortest_name_length": 4}
{"curie": "UMLS:C1334648", "names": ["Meckel Diverticulum NET G1", "Meckel Diverticulum Carcinoid Tumor", "Meckel's Diverticulum Carcinoid Tumor", "Carcinoid Tumor of Meckel's Diverticulum", "Meckel Diverticulum Neuroendocrine Tumor G1", "Carcinoid Tumor of the Meckel's Diverticulum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meckel Diverticulum Neuroendocrine Tumor G1", "shortest_name_length": 26}
{"curie": "MONDO:0008267", "names": ["OFD5", "Ofds 5", "OFDS V", "OFD syndrome 5", "THURSTON SYNDROME", "Thurston syndrome", "OROFACIODIGITAL SYNDROME V", "Orofaciodigital syndrome 5", "Orofaciodigital syndrome V", "orofaciodigital syndrome V", "orofaciodigital syndrome 5", "oral-facial-digital syndrome 5", "oral facial digital syndrome 5", "Oral-facial-digital syndrome 5", "orofaciodigital syndrome type V", "Orofaciodigital syndrome type 5", "orofaciodigital syndrome type 5", "Oro-facial digital syndrome type 5", "oral facial digital syndrome type 5", "Oral-facial-digital syndrome type 5", "oral-facial-digital syndrome type 5", "Oral-Facial-Digital Syndrome, Type V", "ORAL-FACIAL-DIGITAL SYNDROME, TYPE V", "oral-Facial-digital syndrome, type 5", "orofaciodigital syndrome Thurston type", "Orofaciodigital syndrome Thurston type", "orofaciodigital syndrome, Thurston type", "OROFACIODIGITAL SYNDROME, THURSTON TYPE", "Orofaciodigital syndrome, Thurston type", "Oro-facial digital syndrome type 5 (disorder)", "oral-facial-digital syndrome type 5 (diagnosis)", "Polydactyly postaxial with median cleft of upper lip", "polydactyly postaxial with median cleft of upper lip", "POLYDACTYLY, POSTAXIAL, WITH MEDIAN CLEFT OF UPPER LIP", "polydactyly, postaxial, with Median cleft of upper lip", "polydactyly, postaxial, with median cleft of upper lip", "Polydactyly, Postaxial, With Median Cleft Of Upper Lip"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orofaciodigital syndrome V", "shortest_name_length": 4}
{"curie": "UMLS:C0003132", "names": ["Anoxic brain injury", "Anoxic Brain Damage", "Anoxic brain damage", "anoxic brain injury", "anoxic brain damage", "brain anoxic damage", "Damage, Anoxic Brain", "Brain Damage, Anoxic", "anoxic brain injuries", "Anoxic encephalopathy", "anoxic encephalopathy", "Anoxic Encephalopathy", "ENCEPHALOPATHY ANOXIC", "encephalopathy anoxic", "Encephalopathy, Anoxic", "Anoxic Encephalopathies", "Anoxic brain damage, NOS", "Encephalopathies, Anoxic", "Anoxic encephalopathy, NOS", "Anoxic brain damage syndrome", "Anoxic encephalopathy syndrome", "Anoxic encephalopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anoxic Encephalopathy", "shortest_name_length": 19}
{"curie": "UMLS:C5419020", "names": ["Ann Arbor Stage IIX (Bulky) Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage IIX (Bulky) Non-Hodgkin Lymphoma", "shortest_name_length": 48}
{"curie": "UMLS:C4520750", "names": ["Stage III Larynx Carcinoma", "stage III laryngeal cancer", "Stage III Laryngeal Cancer", "Laryngeal Cancer, Stage III", "Stage III Laryngeal Carcinoma", "Stage III Carcinoma of Larynx", "Stage III Carcinoma of the Larynx", "Stage III Laryngeal Throat Cancer", "Stage III Laryngeal Cancer AJCC v7", "Stage III Laryngeal Cancer AJCC v6", "Stage III Laryngeal Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Laryngeal Cancer AJCC v6 and v7", "shortest_name_length": 26}
{"curie": "UMLS:C0334467", "names": ["fibrolipoma", "Fibrolipoma", "FIBROLIPOMA, BENIGN", "adipose tissue fibrolipoma", "fibrolipoma of fatty tissue", "Fibrolipoma (morphologic abnormality)", "fibrolipoma of fatty tissue (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fibrolipoma", "shortest_name_length": 11}
{"curie": "UMLS:C4521862", "names": ["Stage 0 Ampulla of Vater Cancer", "Stage 0 Ampulla of Vater Cancer AJCC v8", "Stage 0 Ampulla of Vater Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Ampulla of Vater Cancer AJCC v8", "shortest_name_length": 31}
{"curie": "MONDO:0033373", "names": ["DEE64", "EIEE64", "early infantile epileptic encephalopathy 64", "developmental and epileptic encephalopathy 64", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 64", "epileptic encephalopathy, early infantile, 64", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 64", "developmental and epileptic encephalopathy, 64"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 64", "shortest_name_length": 5}
{"curie": "MONDO:0009561", "names": ["MANSA", "Mannosidoses", "mannosidosis", "Mannosidosis", "Mannosidosis, NOS", "alpha-Mannosidosis", "Alpha-Mannosidosis", "alpha Mannosidosis", "alpha-mannosidosis", "alpha-Mannosidoses", "alpha mannosidosis", "ALPHA-MANNOSIDOSIS", "Alpha-mannosidosis", "Alpha-D-mannosidosis", "Alpha-D-Mannosidosis", "mannosidase deficiency", "Mannosidosis (disorder)", "mannosidosis (diagnosis)", "Alpha-Mannosidosis, Type I", "alpha-Mannosidase deficiency", "alpha-Mannosidase Deficiency", "alpha Mannosidase Deficiency", "alpha-mannosidase deficiency", "Alpha-mannosidase deficiency", "Deficiency, alpha-Mannosidase", "Alpha-mannosidase B deficiency", "Alpha-Mannosidase B Deficiency", "alpha-Mannosidase Deficiencies", "Alpha mannosidase B deficiency", "ALPHA-MANNOSIDASE B DEFICIENCY", "Mannosidase Deficiency Disease", "alpha Mannosidase B Deficiency", "Lysosomal Alpha B Mannosidosis", "Deficiencies, alpha-Mannosidase", "Deficiency of alpha-mannosidase", "Deficiency Disease, Mannosidase", "mannosidosis, alpha B lysosomal", "deficiency of alpha-mannosidase", "Mannosidase Deficiency Diseases", "Mannosidase Deficiency Syndrome", "Mannosidosis, alpha B Lysosomal", "Deficiency Diseases, Mannosidase", "Deficiency Syndrome, Mannosidase", "Diseases, Mannosidase Deficiency", "Mannosidosis, alpha B, Lysosomal", "MANNOSIDOSIS, ALPHA B, LYSOSOMAL", "mannosidosis, ALPHA B, lysosomal", "Mannosidase Deficiency Syndromes", "Deficiency Syndromes, Mannosidase", "mannosidosis, alpha-, types I and II", "Lysosomal alpha D Mannosidase Deficiency", "Lysosomal alpha-D-Mannosidase Deficiency", "LYSOSOMAL ALPHA-D-MANNOSIDASE DEFICIENCY", "lysosomal alpha-D-mannosidase deficiency", "Lysosomal alpha-D-mannosidase deficiency", "lysosomal Alpha-D-mannosidase deficiency", "alpha-D-Mannosidase Deficiency, Lysosomal", "Deficiency, Lysosomal alpha-D-Mannosidase", "Lysosomal alpha-D-Mannosidase Deficiencies", "Deficiency of alpha-mannosidase (disorder)", "Deficiencies, Lysosomal alpha-D-Mannosidase", "alpha-D-Mannosidase Deficiencies, Lysosomal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alpha-mannosidosis", "shortest_name_length": 5}
{"curie": "UMLS:C0334528", "names": ["Trophoblastic malignant teratoma", "malignant trophoblastic teratoma", "trophoblastic malignant teratoma", "Malignant Trophoblastic Teratoma", "Malignant teratoma, trophoblastic", "trophoblastic malignant teratoma (diagnosis)", "teratoma; malignant, trophoblastic, unspecified site", "malignant; teratoma, trophoblastic, unspecified site", "Malignant teratoma, trophoblastic (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Trophoblastic Teratoma", "shortest_name_length": 32}
{"curie": "MONDO:0010233", "names": ["NHBP", "BPNH", "PVNH1", "PVNH4, FORMERLY", "Familial Nodular Heterotopia", "heterotopia familial nodular", "heterotopia, familial nodular", "HETEROTOPIA, FAMILIAL NODULAR", "Heterotopia, Familial Nodular", "Nodular Heterotopia, Familial", "Familial Nodular Heterotopias", "PVH - Periventricular heterotopia", "X-linked periventricular heterotopia", "X-Linked Periventricular Heterotopia", "periventricular nodular heterotopia 1", "periventricular nodular heterotopia 4", "X-Linked Periventricular Heterotopias", "PERIVENTRICULAR NODULAR HETEROTOPIA 1", "Heterotopia, X-Linked Periventricular", "Periventricular Nodular Heterotopia 4", "Periventricular Heterotopia, X-Linked", "Periventricular Heterotopia, X Linked", "Periventricular Nodular Heterotopia 1", "HETEROTOPIA, PERIVENTRICULAR NODULAR, 1", "bilateral periventricular nodular heterotopia", "nodular heterotopia bilateral periventricular", "Bilateral Periventricular Nodular Heterotopia", "heterotopia periventricular X-linked dominant", "nodular heterotopia, bilateral periventricular", "Nodular Heterotopia, Bilateral Periventricular", "NODULAR HETEROTOPIA, BILATERAL PERIVENTRICULAR", "X-linked periventricular heterotopia (disorder)", "heterotopia, periventricular, X-linked dominant", "PERIVENTRICULAR NODULAR HETEROTOPIA 4, FORMERLY", "periventricular nodular heterotopia 4, formerly", "Heterotopia, Periventricular, X-Linked Dominant", "HETEROTOPIA, PERIVENTRICULAR, X-LINKED DOMINANT", "heterotopia, periventricular, 1, X-linked dominant", "heterotopia, periventricular, Ehlers-Danlos variant", "HETEROTOPIA, PERIVENTRICULAR, EHLERS-DANLOS VARIANT", "Heterotopia, Periventricular, Ehlers-Danlos Variant", "heterotopia, periventricular nodular, with Frontometaphyseal dysplasia", "Heterotopia, Periventricular Nodular, with Frontometaphyseal Dysplasia", "HETEROTOPIA, PERIVENTRICULAR NODULAR, WITH FRONTOMETAPHYSEAL DYSPLASIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heterotopia, periventricular, X-linked dominant", "shortest_name_length": 4}
{"curie": "UMLS:C4551538", "names": ["refractory multiple myeloma", "multiple myeloma, recurrent", "Refractory Multiple Myeloma", "multiple myeloma, refractory", "Refractory Plasma Cell Myeloma", "Plasma cell myeloma refractory", "Refractory Multiple Myeloma/Plasma Cell Myeloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Plasma cell myeloma refractory", "shortest_name_length": 27}
{"curie": "MONDO:0006735", "names": ["duodenal reflux", "Duodenal Reflux", "Duodenal Refluxs", "Reflux, Duodenal", "duodenogastric reflux", "Duodenogastric reflux", "Duodenogastric Reflux", "Duodeno Gastric Reflux", "Reflux, Duodenogastric", "Duodeno-Gastric Reflux", "Reflux, Duodeno-Gastric", "DGR - Duodenogastric reflux", "duodenogastric reflux (finding)", "Duodenogastric reflux (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "duodenogastric reflux", "shortest_name_length": 15}
{"curie": "MONDO:0012270", "names": ["CFEOM4", "Cfeom-U", "CFEOM-U", "TUKEL SYNDROME", "Tukel syndrome", "FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 4", "fibrosis of extraocular muscles, congenital, 4", "congenital fibrosis of the extraocular muscles 4", "congenital extraocular muscle fibrosis with ulnar hand anomalies", "Congenital extraocular muscle fibrosis with ulnar hand anomalies", "fibrosis of extraocular muscles, congenital, with ulnar hand anomalies", "Fibrosis Of Extraocular Muscles, Congenital, with Ulnar Hand Anomalies", "FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, WITH ULNAR HAND ANOMALIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tukel syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C4726594", "names": ["Refractory Lymphoblastic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Lymphoblastic Lymphoma", "shortest_name_length": 33}
{"curie": "UMLS:C3812410", "names": ["retinopathy of prematurity stage 0", "Retinopathy of Prematurity Stage 0", "Retinopathy of prematurity stage 0", "Retinopathy of prematurity, stage 0", "Retinopathy of prematurity stage 0 (finding)", "retinopathy of prematurity stage 0 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retinopathy of prematurity stage 0", "shortest_name_length": 34}
{"curie": "UMLS:C1334770", "names": ["Minor Salivary Gland Oat Cell Carcinoma", "Oat Cell Carcinoma of Minor Salivary Gland", "Minor Salivary Gland Neuroendocrine Carcinoma", "Oat Cell Carcinoma of the Minor Salivary Gland", "Neuroendocrine Carcinoma of Minor Salivary Gland", "Neuroendocrine Carcinoma of the Minor Salivary Gland", "Minor Salivary Gland Small Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Minor Salivary Gland Small Cell Neuroendocrine Carcinoma", "shortest_name_length": 39}
{"curie": "MONDO:0007038", "names": ["ACHOO SYNDROME", "Achoo syndrome", "Peroutka sneeze", "PEROUTKA SNEEZE", "photic sneeze reflex", "Photic sneeze reflex", "PHOTIC SNEEZE REFLEX", "sneezing from Light exposure", "SNEEZING FROM LIGHT EXPOSURE", "autosomal dominant compelling Helioophthalmic outburst syndrome", "Autosomal Dominant Compelling Helioophthalmic Outburst Syndrome", "AUTOSOMAL DOMINANT COMPELLING HELIOOPHTHALMIC OUTBURST SYNDROME", "autosomal dominant compelling helio ophthalmic outburst syndrome", "Autosomal dominant compelling helio ophthalmic outburst syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Achoo syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C5420406", "names": ["Maxillofacial Chondrosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Maxillofacial Chondrosarcoma", "shortest_name_length": 28}
{"curie": "MONDO:0001690", "names": ["Parasitic conjunctivitis", "parasitic conjunctivitis", "Parasitic conjunctivitis, NOS", "Parasitic conjunctivitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parasitic conjunctivitis", "shortest_name_length": 24}
{"curie": "MONDO:0016975", "names": ["mixed thymoma", "Thymoma type AB", "Thymoma Type AB", "type AB thymoma", "thymoma type AB", "Mixed Type Thymoma", "mixed type thymoma", "thymoma, mixed type", "Thymoma, mixed type", "Thymoma, type AB, NOS", "Thymoma type AB (disorder)", "type AB thymoma (diagnosis)", "Primary thymic epithelial tumor type AB", "primary thymic epithelial tumor type AB", "Primary thymic epithelial neoplasm type AB", "primary thymic epithelial neoplasm type AB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thymoma type AB", "shortest_name_length": 13}
{"curie": "MONDO:0007376", "names": ["CFD", "FCD", "Cfd", "fleck corneal dystrophy", "Fleck corneal dystrophy", "corneal dystrophy Fleck", "Fleck Corneal Dystrophy", "corneal fleck dystrophy", "FLECK CORNEAL DYSTROPHY", "Corneal Dystrophy, Fleck", "CORNEAL DYSTROPHY, FLECK", "corneal dystrophy, FLECK", "Fleck corneal dystrophy (disorder)", "Fleck corneal dystrophy (diagnosis)", "François-Neetens speckled corneal dystrophy", "Francois-Neetens speckled corneal dystrophy", "FranC'ois-Neetens speckled corneal dystrophy", "Corneal Dystrophy, Francois-Neetens Speckled or Flecked", "corneal dystrophy, Francois-Neetens speckled or flecked", "CORNEAL DYSTROPHY, FRANCOIS-NEETENS SPECKLED OR FLECKED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fleck corneal dystrophy", "shortest_name_length": 3}
{"curie": "MONDO:0012777", "names": ["CELIAC8", "celiac disease, susceptibility to, 8", "CELIAC DISEASE, SUSCEPTIBILITY TO, 8", "gluten-sensitive enteropathy, susceptibility to, 8", "GLUTEN-SENSITIVE ENTEROPATHY, SUSCEPTIBILITY TO, 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "celiac disease, susceptibility to, 8", "shortest_name_length": 7}
{"curie": "UMLS:C0028431", "names": ["Acquired Nose Deformity", "Acquired nasal deformity", "Nose Deformity, Acquired", "Acquired anomaly of nose", "Acquired Nasal Deformity", "Nasal Deformity, Acquired", "Acquired Nose Deformities", "Nose Deformities, Acquired", "Acquired Nasal Deformities", "Acquired deformity of nose", "acquired deformity of nose", "Acquired Deformity of Nose", "Nasal Deformities, Acquired", "Acquired deformity of nose (disorder)", "acquired deformity of nose (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nose Deformities, Acquired", "shortest_name_length": 23}
{"curie": "MONDO:0022983", "names": ["Dieterich disease", "Dieterich's disease", "avascular necrosis of the metacarpal head", "Avascular necrosis of the metacarpal head"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dieterich disease", "shortest_name_length": 17}
{"curie": "MONDO:0003090", "names": ["extrahepatic bile duct cancer", "Extrahepatic Bile Duct Cancer", "extrahepatic bile duct carcinoma", "Extrahepatic bile duct carcinoma", "Extrahepatic Bile Duct Carcinoma", "BILE DUCT, EXTRAHEPATIC, CARCINOMA", "carcinoma of extrahepatic bile duct", "Carcinoma of Extrahepatic Bile Duct", "Carcinoma of extrahepatic bile duct", "carcinoma of the extrahepatic bile duct", "Carcinoma of the Extrahepatic Bile Duct", "EXTRAHEPATIC BILE DUCT CANCER, CARCINOMA", "Carcinoma of extrahepatic bile duct (disorder)", "carcinoma of extrahepatic bile duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extrahepatic bile duct carcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0012328", "names": ["wen", "Wen", "TRICY1", "PILAR CYST", "Pilar cyst", "pilar cyst", "Pilar Cyst", "pilar; cyst", "Cyst, Pilar", "pilar cysts", "cyst; pilar", "Pilar Cysts", "Cyst, pilar", "Cysts, Pilar", "Trichilemmal cyst", "Tricholemmal Cyst", "trichilemmal cyst", "TRICHOLEMMAL CYST", "Tricholemmal cyst", "Trichilemmal cysts", "cyst; trichilemmal", "trichilemmal; cyst", "trichilemmal cyst 1", "TRICHILEMMAL CYST 1", "Trichilemmal Cyst 1", "Isthmus catagen cyst", "pilar cyst (diagnosis)", "Follicular isthmus cyst", "Trichilemmal cyst (disorder)", "Trichilemmal cyst (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichilemmal cyst", "shortest_name_length": 3}
{"curie": "UMLS:C5555543", "names": ["Recurrent Pineal Parenchymal Cell Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Pineal Parenchymal Cell Neoplasm", "shortest_name_length": 42}
{"curie": "MONDO:0011153", "names": ["HHF2", "nesidioblastosis", "hyperinsulinism, familial", "hyperinsulinism, neonatal", "hyperinsulinism, congenital", "hyperinsulinemic hypoglycemia familial 2", "familial hyperinsulinemic hypoglycemia 2", "hyperinsulinemic hypoglycemia, persistent", "Hyperinsulinemic hypoglycemia, familial, 2", "HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 2", "Hyperinsulinemic Hypoglycemia, Familial, 2", "hyperinsulinemic hypoglycemia, familial, 2", "KCNJ11 hyperinsulinemic hypoglycemia (disease)", "hyperinsulinemic hypoglycemia, familial, type 2", "persistent hyperinsulinemic hypoglycemia of infancy", "hyperinsulinemic hypoglycemia due to Kir6.2 deficiency", "hyperinsulinemic hypoglycemia due to focal adenomatous hyperplasia", "HYPERINSULINEMIC HYPOGLYCEMIA DUE TO FOCAL ADENOMATOUS HYPERPLASIA", "hyperinsulinemic hypoglycemia (disease) caused by mutation in KCNJ11", "Autosomal recessive hyperinsulinemic hypoglycemia due to Kir6.2 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperinsulinemic hypoglycemia, familial, 2", "shortest_name_length": 4}
{"curie": "UMLS:C3641105", "names": ["Postnatal Drug Withdrawal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postnatal Drug Withdrawal", "shortest_name_length": 25}
{"curie": "UMLS:C4524681", "names": ["Breast Carcinoma Metastatic in the CNS", "Metastatic Breast Cancer in the Central Nervous System", "Breast Carcinoma Metastatic in the Central Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Carcinoma Metastatic in the Central Nervous System", "shortest_name_length": 38}
{"curie": "MONDO:0016691", "names": ["Spongioblastoma", "Spongioblastomas", "Piloid astrocytoma", "Spongioblastoma NOS", "Grade I Astrocytoma", "grade I astrocytoma", "Grade 1 Astrocytoma", "astrocytoma, benign", "Spongioblastoma, NOS", "Pilocytic Astrocytoma", "Pilocytic astrocytoma", "pilocytic astrocytoma", "astrocytoma pilocytic", "pilocytic astrocytomas", "Astrocytoma, Pilocytic", "Pilocytic Astrocytomas", "grade I astrocytic tumor", "Grade I Astrocytic Tumor", "Grade 1 Astrocytic Tumor", "grade I Astrocytic tumor", "Grade 1 Astrocytic Neoplasm", "grade I astrocytic neoplasm", "Grade I Astrocytic Neoplasm", "astrocytoma, pilocytic, benign", "Pilocytic astrocytoma (disorder)", "Pilocytic astrocytoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pilocytic astrocytoma", "shortest_name_length": 15}
{"curie": "UMLS:C4288006", "names": ["Vulvar Large Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Large Cell Neuroendocrine Carcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0025459", "names": ["rinderpest", "Rinderpest", "RP infection", "Cattle Plague", "Cattle plague", "cattle plague", "Plague, Cattle", "plague, cattle", "Rinderpest (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rinderpest", "shortest_name_length": 10}
{"curie": "MONDO:0008486", "names": ["Natal teeth and steatocystoma multiplex", "STEATOCYSTOMA multiplex with NATAL teeth", "STEATOCYSTOMA MULTIPLEX WITH NATAL TEETH", "Steatocystoma multiplex with natal teeth", "steatocystoma multiplex-natal teeth syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "steatocystoma multiplex-natal teeth syndrome", "shortest_name_length": 39}
{"curie": "UMLS:C0854967", "names": ["penis cancer, stage III", "stage III penile cancer", "penile cancer, stage III", "Penis carcinoma stage III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Penis carcinoma stage III", "shortest_name_length": 23}
{"curie": "MONDO:0002250", "names": ["Basilar Insufficiency", "Basilar insufficiency", "Insufficiency;basilar", "basilar insufficiency", "a.basilaris; syndrome", "Insufficiency, Basilar", "Basilar Artery Ischemia", "basilar artery syndrome", "Basilar Insufficiencies", "artery basilar syndrome", "Basilar Artery Syndrome", "Basilar artery syndrome", "Artery Ischemia, Basilar", "Basilar Artery Ischemias", "Ischemia, Basilar Artery", "syndrome; basilar artery", "Insufficiencies, Basilar", "Ischemias, Basilar Artery", "Artery Ischemias, Basilar", "a.basilaris; insufficiency", "Basilar Artery Insufficiency", "basilar artery insufficiency", "insufficiency; basilar artery", "Artery Insufficiency, Basilar", "Insufficiency, Basilar Artery", "Insufficiency - basilar artery", "Basilar Artery Insufficiencies", "Insufficiencies, Basilar Artery", "Artery Insufficiencies, Basilar", "Basilar artery syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "basilar artery insufficiency", "shortest_name_length": 21}
{"curie": "UMLS:C3540828", "names": ["Miscellaneous Neoplasm", "Miscellaneous neoplasm, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Miscellaneous Neoplasm", "shortest_name_length": 22}
{"curie": "MONDO:0011901", "names": ["CMT2H", "Cmt2h", "CMT 2H", "AR-CMT2C", "autosomal recessive axonal CMT4C2", "Autosomal recessive axonal CMT4C2", "Charcot Marie Tooth disease type 2H", "Charcot-Marie-Tooth disease type 2H", "Charcot-Marie-Tooth disease, Type 2H", "Charcot-Marie-Tooth disease axonal type 2H", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2H", "Charcot-Marie-Tooth disease, axonal, Type 2H", "Charcot-Marie-Tooth disease, axonal, type 2H", "Charcot-Marie-Tooth disease type 2H (disorder)", "Charcot-Marie-Tooth disease type 2H (diagnosis)", "Axonal Charcot-Marie-Tooth disease with pyramidal involvement", "axonal Charcot-Marie-Tooth disease with pyramidal involvement", "autosomal recessive axonal Charcot-Marie-Tooth disease with pyramidal features", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH PYRAMIDAL FEATURES, AUTOSOMAL RECESSIVE", "autosomal recessive axonal Charcot-Marie-Tooth neuropathy with pyramidal features", "Charcot-Marie-Tooth disease, axonal, with pyramidal features, autosomal recessive", "CHARCOT-MARIE-TOOTH NEUROPATHY, AXONAL, WITH PYRAMIDAL FEATURES, AUTOSOMAL RECESSIVE", "Charcot-Marie-Tooth Neuropathy, Axonal, With Pyramidal Features, Autosomal Recessive", "Charcot-Marie-Tooth neuropathy, axonal, with pyramidal features, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease axonal type 2H", "shortest_name_length": 5}
{"curie": "MONDO:0014020", "names": ["SPG55", "hereditary spastic paraplegia 55", "hereditary spastic paraplegia type 55", "autosomal recessive spastic paraplegia 55", "SPASTIC PARAPLEGIA 55, AUTOSOMAL RECESSIVE", "spastic paraplegia 55, autosomal recessive", "autosomal recessive spastic paraplegia type 55", "Autosomal recessive spastic paraplegia type 55", "familial spastic paraplegia autosomal recessive type 55", "Autosomal recessive spastic paraplegia type 55 (disorder)", "Autosomal recessive spastic paraplegia type 55 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 55", "shortest_name_length": 5}
{"curie": "UMLS:C0027612", "names": ["Congenital, Hereditary, and Neonatal Diseases and Abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital, Hereditary, and Neonatal Diseases and Abnormalities", "shortest_name_length": 63}
{"curie": "UMLS:C0412857", "names": ["Poisoning by sodium valproate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Poisoning by sodium valproate", "shortest_name_length": 29}
{"curie": "MONDO:0013038", "names": ["CLOVE syndrome", "Clove Syndrome", "CLOVE SYNDROME", "CLOVE Syndrome", "Cloves Syndrome", "CLOVES syndrome", "CLOVES Syndrome", "CLOVES SYNDROME", "CLOVE syndrome, somatic", "congenital lipomatous overgrowth - vascular malformation - epidermal nevi", "Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi", "CONGENITAL LIPOMATOUS OVERGROWTH, VASCULAR MALFORMATIONS, AND EPIDERMAL NEVI", "congenital lipomatous overgrowth, vascular malformations, and epidermal nevi", "congenital lipomatous overgrowth, vascular malformations, and EPIDERMAL nevi", "Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi Syndrome", "Congenital lipomatous overgrowth-vascular malformation-epidermal nevi-spinal anomaly syndrome", "congenital lipomatous overgrowth-vascular malformation-epidermal nevi-spinal anomaly syndrome", "Congenital lipomatous overgrowth-vascular malformation-epidermal nevi-skeletal anomaly syndrome", "congenital lipomatous overgrowth-vascular malformation-epidermal nevi-skeletal anomaly syndrome", "Congenital lipomatous overgrowth, vascular malformation, epidermal nevi, skeletal anomaly syndrome", "Congenital lipomatous overgrowth, vascular malformation, epidermal naevi, skeletal anomaly syndrome", "CONGENITAL LIPOMATOUS OVERGROWTH, VASCULAR MALFORMATIONS, EPIDERMAL NEVI, AND SKELETAL/SPINAL ABNORMALITIES", "congenital lipomatous overgrowth, vascular malformations, Epidermal nevi, and skeletal/spinal abnormalities", "Congenital Lipomatous Overgrowth, Vascular Malformations, Epidermal Nevi, and Skeletal-Spinal Abnormalities", "Congenital lipomatous overgrowth, vascular malformation, epidermal nevi, skeletal anomaly syndrome (disorder)", "Congenital Lipomatous Overgrowth, Vascular Malformations, Epidermal Nevi, and Skeletal/Spinal Abnormalities Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CLOVES syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0004568", "names": ["bowel ileus", "adynamic ileus", "Adynamic ileus", "Ileus;paralytic", "ILEUS, ADYNAMIC", "ileus; adynamic", "Paralytic ileus", "Ileus paralytic", "adynamic; ileus", "paralytic ileus", "ileus paralytic", "Paralysis ileum", "Paralytic Ileus", "PARLAYSIS ILEUM", "ILEUS PARALYTIC", "ILEUS, PARALYTIC", "paralysis; bowel", "ileus; paralytic", "bowel; paralysis", "ileus; paralysis", "paralysis; ileus", "paralytic; ileus", "ILEUS, INHIBITORY", "Paralysis of bowel", "intestine paralysis", "intestinal paralysis", "paralysis intestinal", "Paralysis intestinal", "ILEUS, NON-MECHANICAL", "Paralysis of intestine", "paralytic ileus (disease)", "Paralytic ileus (disorder)", "paralytic ileus (diagnosis)", "bowel; obstruction, adynamic", "obstruction; bowel, adynamic", "Paralysis of intestine or colon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paralytic ileus", "shortest_name_length": 11}
{"curie": "MONDO:0011511", "names": ["Chzam", "CHZAM", "clavicular hypoplasia, zygomatic arch hypoplasia, and micrognathia", "Clavicular Hypoplasia, Zygomatic Arch Hypoplasia, and Micrognathia", "CLAVICULAR HYPOPLASIA, ZYGOMATIC ARCH HYPOPLASIA, AND MICROGNATHIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "clavicular hypoplasia, zygomatic arch hypoplasia, and micrognathia", "shortest_name_length": 5}
{"curie": "UMLS:C4524963", "names": ["stage II small intestine cancer", "Stage II Small Intestinal Adenocarcinoma", "Stage II Small Intestinal Adenocarcinoma AJCC v8", "stage II small intestinal adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Small Intestinal Adenocarcinoma AJCC v8", "shortest_name_length": 31}
{"curie": "MONDO:0012078", "names": ["JBTS3", "Joubert syndrome 3", "Joubert Syndrome 3", "JOUBERT SYNDROME 3", "AHI1 Joubert syndrome", "Joubert syndrome type 3", "Joubert syndrome caused by mutation in AHI1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome 3", "shortest_name_length": 5}
{"curie": "MONDO:0006351", "names": ["parachordoma", "Parachordoma", "Parachordoma (disorder)", "Parachordoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parachordoma", "shortest_name_length": 12}
{"curie": "UMLS:C0677950", "names": ["Colorectal cancer Dukes D", "Colorectal cancer stage IV", "stage IV colorectal cancer", "Stage IV Colorectal Cancer", "Dukes D Colorectal Carcinoma", "Astler-Coller D Colorectal Cancer", "Stage IV Colorectal Cancer AJCC v6", "Colorectal Cancer, Stage IV AJCC v6", "Stage IV Colorectal Carcinoma AJCC v6", "Colorectal Carcinoma Stage IV AJCC v6", "Stage IV Colorectal (Colon or Rectal) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Colorectal Cancer", "shortest_name_length": 25}
{"curie": "UMLS:C1709253", "names": ["Non-Neoplastic Vision Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Vision Disorder", "shortest_name_length": 30}
{"curie": "UMLS:C1868753", "names": ["Procedural vomiting"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Procedural vomiting", "shortest_name_length": 19}
{"curie": "UMLS:C1332580", "names": ["Bone Lipoma", "Lipoma of Bone", "lipoma of bone", "Lipoma of the Bone", "lipoma of bone (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lipoma of bone", "shortest_name_length": 11}
{"curie": "MONDO:0035685", "names": ["EBS with extracutaneous involvement", "epidermolysis bullosa simplex with extracutaneous involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolysis bullosa simplex with extracutaneous involvement", "shortest_name_length": 35}
{"curie": "MONDO:0012062", "names": ["CMD1O", "dilated cardiomyopathy 1O", "Cardiomyopathy, Dilated, 1o", "CARDIOMYOPATHY, DILATED, 1O", "cardiomyopathy, dilated, 1O", "dilated cardiomyopathy type 1O", "cardiomyopathy, dilated, type 1O", "ABCC9 familial isolated dilated cardiomyopathy", "dilated cardiomyopathy with ventricular tachycardia", "cardiomyopathy, dilated, with ventricular tachycardia", "CARDIOMYOPATHY, DILATED, WITH VENTRICULAR TACHYCARDIA", "Cardiomyopathy, Dilated, with Ventricular Tachycardia", "familial isolated dilated cardiomyopathy caused by mutation in ABCC9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1O", "shortest_name_length": 5}
{"curie": "MONDO:0014374", "names": ["NPHP18", "nephronophthisis 18", "NEPHRONOPHTHISIS 18", "nephronophthisis type 18", "CEP83 nephronophthisis (disease)", "nephronophthisis (disease) caused by mutation in CEP83"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephronophthisis 18", "shortest_name_length": 6}
{"curie": "UMLS:C1563709", "names": ["Myopathic Ophthalmopathy", "Ophthalmopathy, Myopathic", "Myopathic Ophthalmopathies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myopathic Ophthalmopathy", "shortest_name_length": 24}
{"curie": "MONDO:0018877", "names": ["RPA", "RETINITIS PUNCTATA ALBESCENS", "Retinitis Punctata Albescens", "retinitis punctata albescens", "Retinitis punctata albescens", "punctata albescens; retinitis", "retinitis; punctata albescens", "Retinitis punctata albescens (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis punctata albescens", "shortest_name_length": 3}
{"curie": "MONDO:0009025", "names": ["AME", "APE", "AME1", "Ame1", "AME 1", "Ulick syndrome", "Apparent Mineralocorticoid Excess", "apparent mineralocorticoid excess", "Apparent mineralocorticoid excess", "APPARENT MINERALOCORTICOID EXCESS", "apparent mineralocorticoid EXCESS", "AME - apparent mineralocorticoid excess", "cortisol 11-Beta-ketoreductase deficiency", "cortisol 11-beta-ketoreductase deficiency", "CORTISOL 11-BETA-KETOREDUCTASE DEFICIENCY", "Cortisol 11-beta-ketoreductase deficiency", "Apparent Mineralocorticoid Excess Syndrome", "apparent mineralocorticoid excess syndrome", "Mineralocorticoid Excess Syndrome, Apparent", "Syndrome of Apparent Mineralocorticoid Excess", "Syndrome of apparent mineralocorticoid excess", "syndrome of apparent mineralocorticoid excess", "syndrome of apparent mineralocorticoid Excess", "11 Beta-hydroxysteroid dehydrogenase type 2 deficiency", "11-beta-hydroxysteroid dehydrogenase deficiency type 2", "11 Beta-Hydroxysteroid Dehydrogenase Type 2 Deficiency", "Syndrome of apparent mineralocorticoid excess (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "apparent mineralocorticoid excess", "shortest_name_length": 3}
{"curie": "MONDO:0006765", "names": ["Infection due to Fusobacterium", "infection due to Fusobacterium", "Fusobacterium infectious disease", "Fusobacterium disease or disorder", "infection caused by Fusobacterium", "Infection caused by Fusobacterium", "Fusobacterium caused disease or disorder", "Infection caused by Fusobacterium (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fusobacterium infectious disease", "shortest_name_length": 30}
{"curie": "MONDO:0010160", "names": ["TYRSN2", "tyrosinemia II", "Tat deficiency", "tyrosinosis II", "Tat Deficiency", "Tyrosinemia II", "TAT DEFICIENCY", "Deficiency, Tat", "Tat Deficiencies", "Richner syndrome", "Deficiencies, Tat", "Tyrosinemia type 2", "tyrosinemia type 2", "Type 2 Tyrosinemia", "tyrosinemia, type 2", "hypertyrosinemia II", "Tyrosinemia type II", "Type 2 Tyrosinemias", "Tyrosinemia Type II", "Type II Tyrosinemia", "Tyrosinaemia type 2", "tyrosinemia type II", "Tyrosinemia, Type 2", "Type II Tyrosinemias", "TYROSINEMIA, TYPE II", "Tyrosinaemia type II", "Tyrosinemias, Type 2", "Tyrosinemia, type II", "tyrosinemia, type II", "2 Tyrosinemias, Type", "Tyrosinemia, Type II", "Tyrosinemias, Type II", "Oregon Type Tyrosinemia", "OREGON TYPE TYROSINEMIA", "Oregon type tyrosinemia", "Oregon-type tyrosinemia", "RICHNER-HANHART SYNDROME", "Richner-Hanhart syndrome", "Richner-Hanhart Syndrome", "Richner Hanhart syndrome", "Richner Hanhart Syndrome", "Richner-Hanhart Syndromes", "Syndrome, Richner-Hanhart", "Oculocutaneous tyrosinemia", "oculocutaneous tyrosinemia", "Syndromes, Richner-Hanhart", "Oculocutaneous tyrosinaemia", "Persistent hypertyrosinemia", "Persistent hypertyrosinaemia", "Hypertyrosinemia, Oregon type", "Hypertyrosinaemia, Oregon type", "Oculocutaneous Type Tyrosinosis", "Tyrosinosis oculocutaneous type", "tyrosinemia type II (diagnosis)", "Hereditary Tyrosinemia, Type II", "Oculocutaneous Type Tyrosinoses", "tyrosine transaminase deficiency", "Tyrosine transaminase deficiency", "Tyrosinoses, Oculocutaneous Type", "Tyrosine Transaminase Deficiency", "TYROSINOSIS, OCULOCUTANEOUS TYPE", "Type Tyrosinoses, Oculocutaneous", "Type Tyrosinosis, Oculocutaneous", "Tyrosinosis, Oculocutaneous Type", "Tyrosinosis, oculocutaneous type", "TYROSINE TRANSAMINASE DEFICIENCY", "tyrosinemia due to TAT deficiency", "Tyrosinemia due to TAT deficiency", "Hereditary hypertyrosinemia, type II", "tyrosine aminotransferase deficiency", "TYROSINE AMINOTRANSFERASE DEFICIENCY", "Tyrosine Aminotransferase Deficiency", "Hereditary hypertyrosinaemia, type II", "Hypertyrosinemia, Richner-Hanhart type", "Hypertyrosinaemia, Richner-Hanhart type", "Deficiency of tyrosine aminotransferase", "Tyrosine Transaminase Deficiency Disease", "Deficiency Disease, Tyrosine Transaminase", "oculocutaneous tyrosinemia or tyrosinosis", "cytosolic tyrosine transaminase deficiency", "palmar and plantar keratosis and keratitis", "Tyrosinemia without hepatorenal dysfunction", "Tyrosinaemia without hepatorenal dysfunction", "Keratosis Palmoplantaris with Corneal Dystrophy", "KERATOSIS PALMOPLANTARIS WITH CORNEAL DYSTROPHY", "keratosis palmoplantaris with corneal dystrophy", "Keratosis palmoplantaris with corneal dystrophy", "Hypertyrosinemia, Richner-Hanhart type (disorder)", "tyrosine aminotransferase (TAT) deficiency (TATD)", "Deficiency of tyrosine aminotransferase (disorder)", "Keratosis palmoplantaris-corneal dystrophy syndrome", "keratosis palmoplantaris-corneal dystrophy syndrome", "tyrosinemia due to tyrosine aminotransferase deficiency", "Tyrosinemia due to tyrosine aminotransferase deficiency", "Tyrosinaemia due to tyrosine aminotransferase deficiency", "Richner-Hanhart Syndrome, Tyrosinosis, Oculocutaneous Type", "keratosis palmaris et plantaris-corneal dystrophy syndrome", "tyrosinemia-palmar and plantar keratosis-ocular keratitis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tyrosinemia type II", "shortest_name_length": 6}
{"curie": "UMLS:C1336127", "names": ["Stage IA Vulvar Cancer", "Stage IA Vulva Carcinoma AJCC v6", "Stage IA Vulvar Carcinoma AJCC v6", "Stage IA Carcinoma of Vulva AJCC v6", "Stage IA Carcinoma of the Vulva AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Vulvar Carcinoma AJCC v6", "shortest_name_length": 22}
{"curie": "MONDO:0014339", "names": ["SCAR16", "Spinocerebellar Ataxia Type 16", "STUB1 autosomal recessive cerebellar ataxia", "autosomal recessive spinocerebellar ataxia 16", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 16", "spinocerebellar ataxia, autosomal recessive 16", "Spinocerebellar ataxia autosomal recessive type 16", "autosomal recessive spinocerebellar ataxia type 16", "spinocerebellar ataxia autosomal recessive type 16", "spinocerebellar ataxia, autosomal recessive type 16", "SCAR16 - spinocerebellar ataxia autosomal recessive type 16", "autosomal recessive cerebellar ataxia due to STUB1 deficiency", "Autosomal recessive cerebellar ataxia due to STUB1 deficiency", "autosomal recessive cerebellar ataxia caused by mutation in STUB1", "Autosomal recessive cerebellar ataxia due to STIP1 homology and U-box containing protein 1 deficiency", "Autosomal recessive cerebellar ataxia due to STUB1 (STIP1 homology and U-box containing protein 1) deficiency", "Autosomal recessive cerebellar ataxia due to STIP1 homology and U-box containing protein 1 deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive spinocerebellar ataxia 16", "shortest_name_length": 6}
{"curie": "UMLS:C1167767", "names": ["Gallbladder necrosis", "gallbladder necrosis", "necrosis; gallbladder", "gallbladder; necrosis", "Gallbladder Necrotic Lesion", "gallbladder necrosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gallbladder necrosis", "shortest_name_length": 20}
{"curie": "MONDO:0007748", "names": ["HCA2", "Hypercalciuria, Absorptive, 2", "HYPERCALCIURIA, ABSORPTIVE, 2", "hypercalciuria, absorptive, 2", "Familial idiopathic hypercalciuria", "hypercalciuria, absorptive, type 2", "hypercalciuria, familial idiopathic", "HYPERCALCIURIA, FAMILIAL IDIOPATHIC", "Hypercalciuria, Familial Idiopathic", "Familial idiopathic hypercalciuria (disorder)", "hypercalciuria, absorptive, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypercalciuria, absorptive, 2", "shortest_name_length": 4}
{"curie": "UMLS:C0149700", "names": ["OBSTRUCTION GASTRIC", "Obstruction gastric", "gastric obstruction", "GASTRIC OBSTRUCTION", "Gastric Obstruction", "gastric obstructions", "stomach; obstruction", "obstruction; stomach", "obstruction, gastric"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Obstruction", "shortest_name_length": 19}
{"curie": "MONDO:0015164", "names": ["AML and myelodysplastic syndromes related to alkylating agent", "acute myeloid leukemia and myelodysplastic syndromes related to alkylating agent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia and myelodysplastic syndromes related to alkylating agent", "shortest_name_length": 61}
{"curie": "MONDO:0009092", "names": ["NHD", "PLOSL", "Plo-Sl", "PLO-SL", "Nasu-Hakola disease", "brain-bone-fat disease", "Brain-bone-fat disease", "presenile dementia with bone cysts", "Presenile dementia with bone cysts", "dementia, prefrontal, with bone cysts", "Dementia, prefrontal, with bone cysts", "dementia, progressive, with lipomembranous polycystic osteodysplasia", "Dementia, progressive, with lipomembranous polycystic osteodysplasia", "polycystic lipomembranous osteodysplasia with sclerosing leukoencephaly", "POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY", "Polycystic lipomembranous osteodysplasia with sclerosing leucoencephalopathy", "polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy", "Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy", "PLOSL - polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy", "PLOSL - polycystic lipomembranous osteodysplasia with sclerosing leucoencephalopathy", "Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (disorder)", "progressive dementia with lipomembranous polycystic osteodysplasia; brain-bone-fat disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polycystic lipomembranous osteodysplasia with sclerosing leukoencephaly", "shortest_name_length": 3}
{"curie": "MONDO:0013977", "names": ["COXPD13", "combined oxidative phosphorylation deficiency 13", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 13", "Combined oxidative phosphorylation defect type 13", "combined oxidative phosphorylation defect type 13", "PNPT1 combined oxidative phosphorylation deficiency", "combined oxidative phosphorylation deficiency type 13", "COXPD13 - combined oxidative phosphorylation defect type 13", "Combined oxidative phosphorylation defect type 13 (disorder)", "Combined oxidative phosphorylation defect type 13 (diagnosis)", "combined oxidative phosphorylation deficiency caused by mutation in PNPT1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation defect type 13", "shortest_name_length": 7}
{"curie": "UMLS:C0334048", "names": ["Severe", "Severe Dysplasia", "Severe dysplasia", "dysplasia severe", "severe dysplasia", "Severe dysplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Severe dysplasia", "shortest_name_length": 6}
{"curie": "MONDO:0002472", "names": ["Carcinoma in pleomorphic adenoma", "Carcinoma ex-pleomorphic adenoma", "Carcinoma in Pleomorphic Adenoma", "Carcinoma ex Pleomorphic Adenoma", "carcinoma ex pleomorphic adenoma", "carcinoma in pleomorphic adenoma", "Carcinoma ex pleomorphic adenoma", "[M] Carcinoma in pleomorphic adenoma", "carcinoma ex pleomorphic adenoma (diagnosis)", "malignant neoplasm carcinoma ex pleomorphic adenoma", "carcinoma ex pleomorphic adenoma (morphologic abnormality)", "Carcinoma ex pleomorphic adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma ex pleomorphic adenoma", "shortest_name_length": 32}
{"curie": "MONDO:0013723", "names": ["BACTS1", "bacteremia, resistance to", "bacteremia, protection against", "bacteremia, susceptibility to, 1", "BACTEREMIA, SUSCEPTIBILITY TO, 1", "TIRAP bacteremia, susceptibility", "bacteremia, susceptibility to, type 1", "bacteremia, susceptibility caused by mutation in TIRAP"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bacteremia, susceptibility to, 1", "shortest_name_length": 6}
{"curie": "MONDO:0022772", "names": ["Classic Kaposi Sarcoma", "classic Kaposi sarcoma", "Kaposi sarcoma, classic", "Kaposi Sarcoma, Classic", "classic Kaposi's sarcoma", "Classic Kaposi's Sarcoma", "Kaposi's sarcoma classical", "sarcoma, classical Kaposi's", "Kaposi's sarcoma, classical", "Kaposi Sarcoma Classical Type", "Kaposi sarcoma classical type", "Kaposi's sarcoma classical type", "Kaposi's Sarcoma, Classical Type", "Kaposi's sarcoma, classical type", "Classical type hemorrhagic sarcoma", "Classical type haemorrhagic sarcoma", "classical multiple hemorrhagic sarcoma", "multiple hemorrhagic sarcoma, classical", "sarcoma, classical multiple hemorrhagic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "classic Kaposi sarcoma", "shortest_name_length": 22}
{"curie": "MONDO:0012282", "names": ["ALGAZ", "Al Gazali syndrome", "Al-Gazali syndrome", "AL-GAZALI SYNDROME", "Al-Gazali Syndrome", "Al Gazali Lytle syndrome", "Al Gazali-Lytle syndrome", "Al Gazali Al Talabani syndrome", "Al Gazali-Al Talabani syndrome", "eye defects arachnodactyly cardiopathy", "Eye defects-arachnodactyly-cardiopathy syndrome", "Eye defects, arachnodactyly, cardiopathy syndrome", "Eye defects, arachnodactyly, cardiopathy syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Al-Gazali syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0022778", "names": ["cleft lip palate intellectual disability corneal opacity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleft lip palate intellectual disability corneal opacity", "shortest_name_length": 56}
{"curie": "MONDO:0000477", "names": ["Focal dystonia", "focal dystonia", "DYSTONIA FOCAL", "Focal Dystonia", "Dystonia, focal", "focal dystonias", "Dystonia, Focal", "Focal Dystonias", "Dystonias, Focal", "Focal dystonia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal dystonia", "shortest_name_length": 14}
{"curie": "MONDO:0045046", "names": ["inherited thyroid metabolism disease", "Inherited disorder of thyroid metabolism", "inherited disorder of thyroid metabolism", "INHERITED DISORDERS OF THYROID METABOLISM", "Inherited disorder of thyroid metabolism, NOS", "inborn error of thyroid hormone metabolic process", "inborn thyroid hormone metabolic process disorder", "Inherited disorder of thyroid metabolism (disorder)", "rare inborn error of thyroid hormone metabolic process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited thyroid metabolism disease", "shortest_name_length": 36}
{"curie": "UMLS:C1336954", "names": ["Ventral Hernia with Obstruction without Mention of Gangrene"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ventral Hernia with Obstruction without Mention of Gangrene", "shortest_name_length": 59}
{"curie": "UMLS:C4527429", "names": ["ISMCN", "In Situ Mantle Cell Lymphoma", "In Situ Mantle Cell Neoplasia", "In situ mantle cell neoplasia", "In situ mantle cell neoplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "In situ mantle cell neoplasia", "shortest_name_length": 5}
{"curie": "UMLS:C4524187", "names": ["Duodenal-Type Follicular Lymphoma", "Duodenal-type follicular lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Duodenal-type follicular lymphoma", "shortest_name_length": 33}
{"curie": "MONDO:0008555", "names": ["THC2", "thrombocytopenia 2", "THROMBOCYTOPENIA 2", "Thrombocytopenia 2", "thrombocytopenia type 2", "Helmerhorst Heaton Crossen syndrome", "Thrombocytopenia, autosomal dominant", "Thrombocytopenia chromosome breakage", "thrombocytopenia autosomal dominant 2", "thrombocytopenia, autosomal dominant, 2", "THROMBOCYTOPENIA, AUTOSOMAL DOMINANT, 2", "Thrombocytopenia, Autosomal Dominant, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombocytopenia 2", "shortest_name_length": 4}
{"curie": "UMLS:C5420343", "names": ["Advanced Pharyngeal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Pharyngeal Squamous Cell Carcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0009994", "names": ["arms", "RMSA", "ARMS", "RMS2", "RHABDOMYOSARCOMA 2", "Rhabdomyosarcoma 2", "rhabdomyosarcoma 2", "rhabdomyosarcoma type 2", "rhabdomyosarcoma alveolar", "Alveolar Rhabdomyosarcoma", "alveolar rhabdomyosarcoma", "Alveolar rhabdomyosarcoma", "rhabdomyosarcoma; alveolar", "Rhabdomyosarcoma, Alveolar", "alveolar; rhabdomyosarcoma", "rhabdomyosarcoma, alveolar", "alveolar rhabdomyosarcomas", "RHABDOMYOSARCOMA, ALVEOLAR", "Alveolar Rhabdomyosarcomas", "Rhabdomyosarcomas, Alveolar", "alveolar pediatric rhabdomyosarcoma", "Childhood Alveolar Rhabdomyosarcoma", "Alveolar Childhood Rhabdomyosarcoma", "Pediatric Alveolar Rhabdomyosarcoma", "alveolar childhood rhabdomyosarcoma", "alveolar rhabdomyosarcoma (disease)", "pediatric alveolar rhabdomyosarcoma", "rhabdomyosarcoma, pediatric alveolar", "Alveolar rhabdomyosarcoma (disorder)", "childhood rhabdomyosarcoma, alveolar", "pediatric rhabdomyosarcoma, alveolar", "rhabdomyosarcoma, alveolar childhood", "rhabdomyosarcoma, childhood alveolar", "alveolar rhabdomyosarcoma (diagnosis)", "monomorphous round cell rhabdomyosarcoma", "Monomorphous Round Cell Rhabdomyosarcoma", "rhabdomyosarcoma, alveolar, somatic mutation", "rhabdomyosarcoma 2, alveolar, somatic mutation", "Alveolar rhabdomyosarcoma (morphologic abnormality)", "alveolar rhabdomyosarcoma (morphologic abnormality)", "malignant neoplasm myosarcoma rhabdomyosarcoma alveolar"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alveolar rhabdomyosarcoma", "shortest_name_length": 4}
{"curie": "UMLS:C1517112", "names": ["Fallopian Tube Endometrioid Polyp", "Fallopian Tube Endometrioid Adenomatous Polyp"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fallopian Tube Endometrioid Polyp", "shortest_name_length": 33}
{"curie": "MONDO:0021116", "names": ["Luminal A", "Luminal A Breast Cancer", "Luminal A breast cancer", "Luminal A Breast Carcinoma", "Luminal A breast carcinoma", "luminal A breast carcinoma", "Luminal A Subtype of Breast Carcinoma", "Luminal A subtype of breast carcinoma", "Luminal A Estrogen Receptor Positive Subtype of Breast Carcinoma", "Luminal A estrogen receptor positive subtype of breast carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "luminal A breast carcinoma", "shortest_name_length": 9}
{"curie": "UMLS:C1112371", "names": ["Anterior chamber pigmentation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anterior chamber pigmentation", "shortest_name_length": 29}
{"curie": "MONDO:0001533", "names": ["Pes anserinus tendinitis or bursitis", "pes anserinus tendinitis or bursitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pes anserinus tendinitis or bursitis", "shortest_name_length": 36}
{"curie": "UMLS:C0265312", "names": ["Brachydactyly syndrome type E", "Brachydactyly syndrome type E (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brachydactyly syndrome type E", "shortest_name_length": 29}
{"curie": "UMLS:C5554578", "names": ["Unresectable Cervical Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Cervical Squamous Cell Carcinoma", "shortest_name_length": 45}
{"curie": "MONDO:0012971", "names": ["MVCD7", "NEPHROPATHY, DIABETIC, SUSCEPTIBILITY TO", "nephropathy, diabetic, susceptibility to", "microvascular complications of diabetes 7", "proliferative retinopathy, diabetic, susceptibility to", "PROLIFERATIVE RETINOPATHY, DIABETIC, SUSCEPTIBILITY TO", "NONPROLIFERATIVE RETINOPATHY, DIABETIC, SUSCEPTIBILITY TO", "nonproliferative retinopathy, diabetic, susceptibility to", "HFE microvascular complications of diabetes, susceptibility", "MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7", "microvascular complications of diabetes, susceptibility to, 7", "microvascular complications of diabetes, susceptibility to, type 7", "MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding)", "microvascular complications of diabetes, susceptibility caused by mutation in HFE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microvascular complications of diabetes, susceptibility to, 7", "shortest_name_length": 5}
{"curie": "UMLS:C0854834", "names": ["Angioimmunoblastic T-cell lymphoma refractory", "Angioimmunoblastic T-Cell Lymphoma Refractory", "Refractory Angioimmunoblastic T-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Angioimmunoblastic T-cell lymphoma refractory", "shortest_name_length": 45}
{"curie": "UMLS:C4727187", "names": ["Recurrent Ovarian Carcinosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Ovarian Carcinosarcoma", "shortest_name_length": 32}
{"curie": "MONDO:0008591", "names": ["tremor nystagmus duodenal ulcer", "Tremor nystagmus duodenal ulcer", "Neuhauser Daly Magnelli syndrome", "Neuhauser-Daly-Magnelli syndrome", "Tremor, Nystagmus, and Duodenal Ulcer", "TREMOR, NYSTAGMUS, AND DUODENAL ULCER", "tremor, NYSTAGMUS, and duodenal ulcer", "Tremors, nystagmus and duodenal ulcers", "tremor-nystagmus-duodenal ulcer syndrome", "Tremor-nystagmus-duodenal ulcer syndrome", "Tremor, nystagmus, duodenal ulcer syndrome", "Essential tremors, nystagmus and duodenal ulceration", "Tremor, nystagmus, duodenal ulcer syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tremor-nystagmus-duodenal ulcer syndrome", "shortest_name_length": 31}
{"curie": "MONDO:0016580", "names": ["CPAM", "CCAM", "Cystic adenomatoid lung disease", "congenital cystic disease of the lung", "Congenital cystic disease of the lung", "cystic adenomatoid malformation of lung", "Cystic Adenomatoid Malformation of Lung", "congenital pulmonary airway malformation", "Congenital pulmonary airway malformation", "congenital cystic adenomatoid malformation", "Congenital Cystic Adenomatoid Malformation", "Cystic adenomatoid malformation, congenital", "CPAM - Congenital pulmonary airway malformation", "Lung Malformation, Congenital Cystic Adenomatoid", "Lung Malformation, Cystic Adenomatoid, Congenital", "Congenital Cystic Adenomatoid Malformation of Lung", "Congenital cystic adenomatoid malformation of lung", "congenital cystic adenomatoid malformation of lung", "Cystic Adenomatoid Malformation of Lung, Congenital", "congenital cystic adenomatous malformation of the lung", "congenital cystic adenomatoid malformation of the lung", "Congenital Cystic Adenomatoid Malformation of the Lung", "Congenital cystic adenomatoid malformation of the lung", "Congenital cystic adenomatous malformation of the lung", "Congenital cystic adenomatoid malformation of lung (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital pulmonary airway malformation", "shortest_name_length": 4}
{"curie": "MONDO:0030669", "names": ["GIDID2", "multiple intestinal atresia with or without leukopenia", "MULTIPLE INTESTINAL ATRESIA WITH OR WITHOUT LEUKOPENIA", "GASTROINTESTINAL DEFECTS AND IMMUNODEFICIENCY SYNDROME 2", "gastrointestinal defects and immunodeficiency syndrome 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastrointestinal defects and immunodeficiency syndrome 2", "shortest_name_length": 6}
{"curie": "MONDO:0006618", "names": ["VBU", "CIndU", "Vibratory urticaria", "vibratory urticaria", "VIBRATORY URTICARIA", "Vibratory Urticaria", "Urticaria vibratory", "vibration; urticaria", "Urticaria, Vibratory", "Vibratory Urticarias", "urticaria; vibration", "Chronic Inducible Urticaria", "Inducible Urticaria, Chronic", "Chronic Inducible Urticarias", "Vibratory urticaria (disorder)", "vibratory urticaria (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vibratory urticaria", "shortest_name_length": 3}
{"curie": "MONDO:0010743", "names": ["THC", "XLT", "THC1", "THROMBOCYTOPENIA 1", "Thrombocytopenia 1", "thrombocytopenia 1", "XL-Thrombocytopenia", "thrombocytopenia type 1", "X-linked thrombocytopenia", "X-Linked Thrombocytopenia", "Thrombocytopenia, X-Linked", "thrombocytopenia, X-linked", "THROMBOCYTOPENIA, X-LINKED", "Thrombocytopenia, X-Linked, 1", "THROMBOCYTOPENIA, X-LINKED, 1", "thrombocytopenia, X-linked, 1", "THROMBOCYTOPENIA, X-LINKED, INTERMITTENT", "Thrombocytopenia, X-Linked, Intermittent", "thrombocytopenia, X-linked, intermittent", "thrombocytopenia, X-linked, X-linked recessive", "X-linked thrombocytopenia with normal platelets", "thrombocytopenia, X-linked, intermittent, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombocytopenia 1", "shortest_name_length": 3}
{"curie": "UMLS:C4725792", "names": ["Metastatic Urethral Urothelial Cancer", "Metastatic Urethral Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Urethral Urothelial Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0010691", "names": ["ND", "nd", "NDP", "Pseudoglioma", "pseudoglioma", "Norrie disease", "norrie disease", "NORRIE DISEASE", "norrie syndrome", "Norrie Syndrome", "Norrie syndrome", "Norrie's disease", "norrie's disease", "Norrie's Disease", "Episkopi blindness", "episkopi blindness", "EPISKOPI BLINDNESS", "Norrie disease (ND)", "fetal iritis syndrome", "Fetal Iritis Syndrome", "Norrie-Warburg disease", "pseudoglioma congenita", "Pseudoglioma Congenita", "Norrie-Warburg syndrome", "Whitnall-Norman Syndrome", "Anderson-Warburg Syndrome", "Anderson-Warburg syndrome", "Norrie disease (diagnosis)", "Oligophrenia Microphthalmus", "Oligophrenia microphthalmus", "Atrophia bulborum hereditaria", "atrophia bulborum hereditaria", "ATROPHIA BULBORUM HEREDITARIA", "Norrie disease, X-linked recessive", "Atrophia bulborum hereditaria (disorder)", "Congenital Progressive Oculo-Acoustico-Cerebral Degeneration", "congenital progressive oculo-acoustico-cerebral degeneration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Norrie disease", "shortest_name_length": 2}
{"curie": "MONDO:0005296", "names": ["SDB", "SLEEP APNEA", "Sleep Apnea", "Sleep apnea", "sleep apnea", "sleep apnoea", "apnea, sleep", "sleep apneas", "SLEEP APNOEA", "apnea; sleep", "Sleep Apneas", "Sleep apnoea", "sleep; apnea", "Apnea, Sleep", "apneas, sleep", "Apneas, Sleep", "Sleep apnoeas", "Sleep hypopnea", "sleep hypopnea", "Sleep Hypopnea", "Apnea syndrome", "Sleep apnea NOS", "Hypopnea, Sleep", "hypopnea, sleep", "Apnoea syndrome", "Sleep Hypopneas", "sleep hypopneas", "Sleep hypopnoea", "Sleep apnea, NOS", "hypopneas, sleep", "Hypopneas, Sleep", "mixed sleep apnea", "Sleep apnoea, NOS", "sleep apnea, mixed", "mixed sleep Apneas", "sleep apneas, mixed", "SLEEP APNEA SYNDROME", "Sleep Apnea Syndrome", "sleep apnea syndrome", "Sleep apnea syndrome", "Sleep Apnea Syndromes", "sleep apnea syndromes", "apnea syndrome, sleep", "Apnea Syndrome, Sleep", "SLEEP APNOEA SYNDROME", "Sleep apnoea syndrome", "sleep apnoea syndrome", "Sleep apnea syndromes", "Sleep apnoea syndromes", "Sleep apnea (disorder)", "Apnea Syndromes, Sleep", "apnea syndromes, sleep", "Unspecified sleep apnea", "Sleep apnea, unspecified", "Sleep apnoea, unspecified", "SAS - Sleep apnea syndrome", "Sleep Disordered Breathing", "Sleep-disordered Breathing", "Sleep-disordered breathing", "Sleep-Disordered Breathing", "sleep hypopnea (diagnosis)", "sleep-disordered breathing", "sleep disordered breathing", "SAS - Sleep apnoea syndrome", "Breathing, Sleep-Disordered", "breathing, sleep-disordered", "breathing-related sleep disorder", "Breathing-related sleep disorder", "sleep disorder; breathing-related", "Pauses in breathing while sleeping", "breathing disorder during sleeping", "periods of not breathing while asleep", "hypersomnia with periodic respiration", "Breathing-related sleep disorder, NOS", "mixed central and obstructive sleep apnea", "sleep apnea, mixed central and obstructive", "Breathing-related sleep disorder (disorder)", "breathing-related sleep disorder (diagnosis)", "periods of not breathing while asleep (symptom)", "periods of not breathing while asleep (sleep apnea)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sleep apnea syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0013978", "names": ["DFNB70", "autosomal recessive deafness 70", "deafness, autosomal recessive 70", "DEAFNESS, AUTOSOMAL RECESSIVE 70", "deafness, autosomal recessive type 70", "autosomal recessive nonsyndromic deafness 70", "PNPT1 autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 70", "autosomal recessive nonsyndromic deafness type 70", "autosomal recessive nonsyndromic deafness caused by mutation in PNPT1", "DEAFNESS, AUTOSOMAL RECESSIVE 70, WITH OR WITHOUT ADULT-ONSET NEURODEGENERATION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 70", "shortest_name_length": 6}
{"curie": "MONDO:0020129", "names": ["acquired motor neuron disease", "acquired anterior horn cell disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired motor neuron disease", "shortest_name_length": 29}
{"curie": "MONDO:0012167", "names": ["ATFB2", "ATRIAL FIBRILLATION, FAMILIAL, 2", "Atrial Fibrillation, Familial, 2", "atrial fibrillation, familial, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial fibrillation, familial, 2", "shortest_name_length": 5}
{"curie": "MONDO:0012915", "names": ["dup(1)(q21.1)", "trisomy 1q21.1", "1q21.1 microduplication syndrome", "chromosome 1q21.1 duplication syndrome", "Chromosome 1q21.1 Duplication Syndrome", "CHROMOSOME 1q21.1 DUPLICATION SYNDROME", "chromosome 1q21.1 duplication syndrome, isolated cases", "1q21.1 recurrent microduplication (possible susceptibility locus for neurodevelopmental disorders)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 1q21.1 duplication syndrome", "shortest_name_length": 13}
{"curie": "UMLS:C4744704", "names": ["Tongue Alveolar Soft Part Sarcoma'"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tongue Alveolar Soft Part Sarcoma'", "shortest_name_length": 34}
{"curie": "EFO:1001925", "names": ["pneumococcal bacteremia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pneumococcal bacteremia", "shortest_name_length": 23}
{"curie": "MONDO:0003698", "names": ["penis verrucous carcinoma", "verrucous penile carcinoma", "Verrucous Penile Carcinoma", "Verrucous Carcinoma of Penis", "Verrucous carcinoma of penis", "verrucous carcinoma of penis", "verrucous carcinoma of the penis", "Verrucous Carcinoma of the Penis", "Verrucous Penile Squamous Carcinoma", "verrucous penile squamous carcinoma", "verrucous squamous carcinoma of penis", "Verrucous Squamous Carcinoma of Penis", "verrucous penile squamous cell carcinoma", "verrucous carcinoma of penis (diagnosis)", "Verrucous Squamous Carcinoma of the Penis", "verrucous squamous carcinoma of the penis", "squamous carcinoma of penis, verrucous type", "Squamous Carcinoma of Penis, Verrucous Type", "squamous carcinoma of the penis, verrucous type", "Squamous Carcinoma of the Penis, Verrucous Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "penis verrucous carcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0019521", "names": ["RDEB-Ce", "RDEB, centripetalis", "centripetal dystrophic epidermolysis bullosa", "Centripetal recessive dystrophic epidermolysis bullosa", "centripetal recessive dystrophic epidermolysis bullosa", "Centripetalis recessive dystrophic epidermolysis bullosa", "centripetalis recessive dystrophic epidermolysis bullosa", "RDEB-Ce - recessive dystrophic epidermolysis bullosa centripetalis", "Centripetalis recessive dystrophic epidermolysis bullosa (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "centripetalis recessive dystrophic epidermolysis bullosa", "shortest_name_length": 7}
{"curie": "OMIM:615970", "names": ["HPAFP", "Hereditary persistence of alpha-fetoprotein", "ALPHA-FETOPROTEIN, HEREDITARY PERSISTENCE OF", "Hereditary persistence of alpha-fetoprotein (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 5}
{"curie": "UMLS:C1336367", "names": ["Stage IVB Esophagus Squamous Cell Carcinoma", "Stage IVB Esophageal Squamous Cell Carcinoma", "Stage IVB Squamous Cell Carcinoma of Esophagus", "Stage IVB Squamous Cell Carcinoma of the Esophagus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Esophageal Squamous Cell Carcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0019317", "names": ["follicular atrophoderma-basal cell carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "follicular atrophoderma-basal cell carcinoma", "shortest_name_length": 44}
{"curie": "UMLS:C5418790", "names": ["Locally Advanced Rectal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Rectal Squamous Cell Carcinoma", "shortest_name_length": 47}
{"curie": "MONDO:0009478", "names": ["HIES2", "AR-HIES", "DOCK8 Deficiency", "DOCK8 deficiency", "HIES autosomal recessive", "Autosomal Recessive HIES", "Autosomal Recessive HIESs", "HIES, autosomal recessive", "HIES, AUTOSOMAL RECESSIVE", "HIES, Autosomal Recessive", "HIESs, Autosomal Recessive", "Cid due to DOCK8 deficiency", "DOCK8 immunodeficiency syndrome", "AR hyperimmunoglobulin E syndrome", "dedicator of cytokinesis 8 deficiency", "Dedicator of Cytokinesis 8 Deficiency", "Autosomal Recessive hyper IgE syndrome", "autosomal recessive hyper IgE syndrome", "Hyper IgE Syndrome, Autosomal Recessive", "Hyper-IgE Syndrome, Autosomal Recessive", "hyper-IgE syndrome, autosomal recessive", "HYPER-IgE SYNDROME, AUTOSOMAL RECESSIVE", "hyper IgE recurrent infection syndrome 2", "hyper Ig E syndrome, autosomal recessive", "combined immunodeficiency due to DOCK8 deficiency", "Hyper Immunoglobulin E Syndrome, Autosomal Recessive", "Hyper-Immunoglobulin E Syndrome, Autosomal Recessive", "Hyper IgE Recurrent Infection Syndrome, Autosomal Recessive", "Hyper-IgE Recurrent Infection Syndrome, Autosomal Recessive", "hyper-IgE recurrent infection syndrome, autosomal recessive", "HYPER-IgE RECURRENT INFECTION SYNDROME 2, AUTOSOMAL RECESSIVE", "hyperimmunoglobulin E recurrent infection syndrome, autosomal recessive", "combined immunodeficiency due to dedicator of cytokinesis 8 protein deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined immunodeficiency due to DOCK8 deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C4525655", "names": ["Jejunal Neuroendocrine Tumor by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jejunal Neuroendocrine Tumor by AJCC v8 Stage", "shortest_name_length": 45}
{"curie": "MONDO:0013759", "names": ["GEY", "CMM8", "EYCL1", "SHEP3", "EYE COLOR 1", "EYE COLOR, GREEN/BLUE", "SKIN/HAIR/EYE PIGMENTATION 3, FRECKLING", "SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 3", "SKIN/HAIR/EYE PIGMENTATION 3, LIGHT/DARK SKIN", "susceptibility to cutaneous malignant melanoma 8", "SKIN/HAIR/EYE PIGMENTATION 3, BLUE/GREEN EYE COLOR", "melanoma, cutaneous malignant, susceptibility to, 8", "MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 8", "melanoma and renal cell carcinoma, susceptibility to", "MELANOMA AND RENAL CELL CARCINOMA, SUSCEPTIBILITY TO", "melanoma, cutaneous malignant, susceptibility to, type 8", "MITF-related melanoma and renal cell carcinoma predisposition syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melanoma, cutaneous malignant, susceptibility to, 8", "shortest_name_length": 3}
{"curie": "UMLS:C1513734", "names": ["Conventional ameloblastoma", "Intraosseous Ameloblastoma", "Conventional Ameloblastoma", "Solid/Multicystic Ameloblastoma", "Conventional ameloblastoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conventional ameloblastoma", "shortest_name_length": 26}
{"curie": "UMLS:C0154769", "names": ["Myotoxicity", "Myotoxicities", "toxic myopathy", "Toxic myopathy", "Myopathy toxic", "Toxic Myopathy", "myopathy; toxic", "Myopathy, Toxic", "toxic; myopathy", "myopathies toxic", "Toxic Myopathies", "Toxic myopathy, NOS", "Toxic muscle disease", "Toxic myopathy (disorder)", "toxic myopathy (diagnosis)", "myopathy due to toxic agents", "myopathy due to toxic agents (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myotoxicity", "shortest_name_length": 11}
{"curie": "MONDO:0054865", "names": ["encephalopathy due to mitochondrial and peroxisomal fission defect", "encephalopathy due to defective mitochondrial and peroxisomal fission"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephalopathy due to mitochondrial and peroxisomal fission defect", "shortest_name_length": 66}
{"curie": "MONDO:0000616", "names": ["progesterone-receptor negative breast cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progesterone-receptor negative breast cancer", "shortest_name_length": 44}
{"curie": "UMLS:C1336177", "names": ["Stage IIB Bone Sarcoma", "Stage IIB Sarcoma of Bone", "Stage IIB Sarcoma of the Bone", "Stage IIB Bone Sarcoma AJCC v7", "Stage IIB Bone Sarcoma  AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Bone Sarcoma AJCC v7", "shortest_name_length": 22}
{"curie": "MONDO:0005705", "names": ["CLONORCHIASIS", "Clonorchiases", "Clonorchiosis", "Clonorchiasis", "clonorchiasis", "Clonorchis Infection", "Clonorchis Infections", "Infection, Clonorchis", "Clonorchis; infestation", "infestation; Clonorchis", "Clonorchiasis (disorder)", "clonorchiasis (diagnosis)", "Chinese liver fluke disease", "Oriental liver fluke disease", "Clonorchis sinensis infection", "liver fluke disease; oriental", "oriental; liver fluke disease", "Clonorchis sinensis Infection", "Infection, Clonorchis sinensis", "liver; disease, fluke, Chinese", "Clonorchis sinensis Infections", "liver; disease, fluke, oriental", "Opisthorchis sinensis Infection", "Infection, Opisthorchis sinensis", "Opisthorchis sinensis Infections", "fluke; infestation, liver, Chinese", "infestation; fluke, liver, Chinese", "liver; fluke disease, Chinese, oriental", "fluke disease; liver, Chinese, oriental", "disease (or disorder); liver, fluke, Chinese", "disease (or disorder); liver, fluke, oriental", "Hepatic distomiasis due to Clonorchis sinensis", "fluke disease; liver, due to Clonorchis sinensis", "liver; fluke disease, due to Clonorchis sinensis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "clonorchiasis", "shortest_name_length": 13}
{"curie": "MONDO:0044204", "names": ["SDS1", "Shwachman-Bodian syndrome", "Shwachman-Diamond syndrome", "SHWACHMAN-DIAMOND SYNDROME 1", "Shwachman-Diamond syndrome 1", "lipomatosis of pancreas, congenital", "pancreatic insufficiency and bone marrow dysfunction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Shwachman-Diamond syndrome 1", "shortest_name_length": 4}
{"curie": "UMLS:C0948981", "names": ["Persecutory Type Delusional Disorder", "Delusional disorder, persecutory type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Delusional disorder, persecutory type", "shortest_name_length": 36}
{"curie": "MONDO:0008116", "names": ["OPMD", "Oculopharyngeal Dystrophy", "Oculopharyngeal dystrophy", "oculopharyngeal; dystrophy", "dystrophy; oculopharyngeal", "Oculopharyngeal Muscular Dystrophy", "Oculopharyngeal muscular dystrophy", "oculopharyngeal muscular dystrophy", "OCULOPHARYNGEAL MUSCULAR DYSTROPHY", "MUSCULAR DYSTROPHY, OCULOPHARYNGEAL", "Muscular Dystrophy, Oculopharyngeal", "muscular dystrophy, oculopharyngeal", "Muscular dystrophy, oculopharyngeal", "Dystrophy, Oculopharyngeal Muscular", "Oculopharyngeal Muscular Dystrophies", "Dystrophies, Oculopharyngeal Muscular", "Muscular Dystrophies, Oculopharyngeal", "Oculopharyngeal muscular dystrophy (disorder)", "oculopharyngeal muscular dystrophy (diagnosis)", "Progressive muscular dystrophy, oculopharyngeal type", "Progressive Muscular Dystrophy, Oculopharyngeal Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculopharyngeal muscular dystrophy", "shortest_name_length": 4}
{"curie": "UMLS:C0221520", "names": ["Schizophrenia simple", "Simple schizophrenia", "simple schizophrenia", "Simple Schizophrenia", "simple; schizophrenic", "Schizophrenia simplex", "schizophrenia; simple", "schizophrenia simplex", "schizophrenia; simplex", "simplex; schizophrenic", "Simple Type Schizophrenia", "Simple type schizophrenia", "Schizophrenia, simple type", "Simple schizophrenia (disorder)", "simple schizophrenia (diagnosis)", "Simple type schizophrenia, unspecified", "Simple type schizophrenia, unspecified state"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Simple schizophrenia", "shortest_name_length": 20}
{"curie": "UMLS:C1321778", "names": ["Localized Askin Tumor", "Localized Askin's Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized Askin Tumor", "shortest_name_length": 21}
{"curie": "MONDO:0014539", "names": ["FSGS9", "focal segmental glomerulosclerosis 9", "FOCAL SEGMENTAL GLOMERULOSCLEROSIS 9", "glomerulosclerosis, focal segmental, 9", "GLOMERULOSCLEROSIS, FOCAL SEGMENTAL, 9", "CRB2 focal segmental glomerulosclerosis", "focal segmental glomerulosclerosis type 9", "focal segmental glomerulosclerosis caused by mutation in CRB2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal segmental glomerulosclerosis 9", "shortest_name_length": 5}
{"curie": "UMLS:C1335378", "names": ["Pericardial Carcinomatosis", "Carcinomatosis of the Pericardium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pericardial Carcinomatosis", "shortest_name_length": 26}
{"curie": "UMLS:C2986863", "names": ["Thymoliposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thymoliposarcoma", "shortest_name_length": 16}
{"curie": "UMLS:C0233523", "names": ["sociopathy", "SOCIOPATHY", "Sociopathy", "Sociopathology", "sociopathology", "REACTION ASOCIAL", "ASOCIAL REACTION", "Reaction asocial", "Asocial reaction", "Antisocial reaction", "REACTION ANTISOCIAL", "BEHAVIOR ANTISOCIAL", "Reaction antisocial", "Antisocial behavior", "ANTISOCIAL REACTION", "antisocial behavior", "Antisocial Behavior", "antisocial behaviour", "antisocial; behavior", "anti-social behavior", "anti social behavior", "Anti-social behavior", "Behavior, Antisocial", "antisocial behaviors", "behavior; antisocial", "Antisocial Behaviors", "Antisocial behaviour", "anti-social behaviour", "Anti-social behaviour", "Behaviors, Antisocial", "Antisocial behavior (finding)", "antisocial behavior (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Antisocial behavior", "shortest_name_length": 10}
{"curie": "MONDO:0014728", "names": ["COXPD27", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 27", "combined oxidative phosphorylation deficiency 27", "Combined Oxidative Phosphorylation Deficiency 27", "Combined oxidative phosphorylation defect type 27", "combined oxidative phosphorylation defect type 27", "CARS2 combined oxidative phosphorylation deficiency", "combined oxidative phosphorylation deficiency type 27", "COXPD27 - combined oxidative phosphorylation defect type 27", "Combined oxidative phosphorylation defect type 27 (disorder)", "combined oxidative phosphorylation deficiency caused by mutation in CARS2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation defect type 27", "shortest_name_length": 7}
{"curie": "MONDO:0003716", "names": ["renal pelvis papillary carcinoma", "Kidney Pelvis Papillary Carcinoma", "kidney pelvis papillary carcinoma", "Papillary Carcinoma of Renal Pelvis", "papillary carcinoma of renal pelvis", "Papillary carcinoma of renal Pelvis", "Papillary Carcinoma of Kidney Pelvis", "KIDNEY, PELVIS, CARCINOMA, PAPILLARY", "papillary carcinoma of kidney pelvis", "papillary carcinoma of the renal pelvis", "Papillary Carcinoma of the Renal Pelvis", "papillary carcinoma of the kidney pelvis", "Papillary Carcinoma of the Kidney Pelvis", "renal pelvis papillary urothelial carcinoma", "Renal Pelvis Papillary Urothelial Carcinoma", "papillary carcinoma of renal pelvis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal pelvis papillary urothelial carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0018490", "names": ["Cono-spondylar dysplasia", "cono-spondylar dysplasia", "Cono-spondylar dysplasia (disorder)", "short stature-kyphosis-hypoplasia of basal ilia-cone epiphyses-facial dysmorphism syndrome", "Short stature-kyphosis-hypoplasia of basal ilia-cone epiphyses-facial dysmorphism syndrome", "Short stature, kyphosis, hypoplasia of basal ilia-cone epiphyses, facial dysmorphism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cono-spondylar dysplasia", "shortest_name_length": 24}
{"curie": "MONDO:0018214", "names": ["GEFS+", "genetic epilepsy with febrile seizures-plus", "genetic epilepsy with febrile seizures plus", "Genetic epilepsy with febrile seizures-plus", "Generalised epilepsy with febrile seizures plus", "Generalized epilepsy with febrile seizures-plus", "Generalized Epilepsy with Febrile Seizures Plus", "generalized epilepsy with febrile seizures-plus", "generalized epilepsy with febrile seizures plus", "epilepsy generalized with febrile seizures plus", "Generalized epilepsy with febrile seizures plus", "epilepsy, generalized, with febrile seizures plus", "Generalized epilepsy with febrile seizures plus (disorder)", "Generalized epilepsy with febrile seizures plus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "generalized epilepsy with febrile seizures plus", "shortest_name_length": 5}
{"curie": "MONDO:0003738", "names": ["Selective IgE deficiency", "Selective IgE Immunodeficiency", "selective IgE immunodeficiency", "selective IgE deficiency disease", "Selective immunoglobulin E deficiency", "selective immunoglobulin E deficiency", "Selective immunoglobulin E deficiency (disorder)", "Selective immunoglobulin E deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "selective IgE deficiency disease", "shortest_name_length": 24}
{"curie": "UMLS:C1696087", "names": ["Uterine Fistula", "Uterine fistula"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Fistula", "shortest_name_length": 15}
{"curie": "MONDO:0004190", "names": ["Bladder Nephrogenic Adenoma", "Urinary Bladder Nephrogenic Adenoma", "urinary bladder nephrogenic adenoma", "Nephrogenic Adenoma of Urinary Bladder", "nephrogenic adenoma of urinary bladder", "nephrogenic adenoma of the urinary bladder", "Nephrogenic Adenoma of the Urinary Bladder", "Nephrogenic adenoma of the urinary bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrogenic adenoma of urinary bladder", "shortest_name_length": 27}
{"curie": "MONDO:0002378", "names": ["Dermoid", "dermoid", "Dermoids", "dermoids", "horn cyst", "DERMOID CYST", "Dermoid Cyst", "dermoid cyst", "Dermoid cyst", "Dermoid, NOS", "Cyst;dermoid", "Dermoid Tumor", "Dermoid tumor", "Dermoid sinus", "Cyst, Dermoid", "Dermoid Cysts", "dermoid tumor", "dermoid cysts", "Dermoid tumour", "Cysts, Dermoid", "dermoid tumour", "benign teratoma", "[M]Dermoid cyst", "mature teratoma", "cystic teratoma", "teratoma, benign", "Dermoid cyst NOS", "Dermoid cyst, NOS", "Dermoid choristoma", "dermoid choristoma", "DERMOID CYST, BENIGN", "dermoid cyst, benign", "Mature Cystic Teratoma", "mature cystic teratoma", "Mature cystic teratoma", "benign cystic teratoma", "Benign Cystic Teratoma", "Dermoid cyst (disorder)", "Cystic dermoid choristoma", "cystic dermoid choristoma", "subcutaneous cystic teratoma", "Subcutaneous Cystic Teratoma", "Dermoid cyst (morphologic abnormality)", "Dermoid tumor (morphologic abnormality)", "teratoma, benign (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermoid cyst", "shortest_name_length": 7}
{"curie": "UMLS:C4553620", "names": ["I", "Stage I Cervical Cancer", "Stage I Cervical Cancer AJCC v8", "Stage I Cervical Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Cervical Cancer AJCC v8", "shortest_name_length": 1}
{"curie": "MONDO:0001258", "names": ["a.vertebralis; occlusion", "Vertebral artery occlusion", "vertebral artery occlusion", "occlusion; vertebral artery", "Vertebral artery obstruction", "obstruction; vertebral artery", "vertebrobasial artery occlusion", "Vertebral artery occlusion (disorder)", "vertebral artery occlusion (diagnosis)", "Vertebral artery obstruction (disorder)", "occlusion and stenosis of vertebral artery", "Occlusion and stenosis of vertebral artery"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vertebral artery occlusion", "shortest_name_length": 24}
{"curie": "MONDO:0012619", "names": ["MRT11", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 11", "mental retardation, autosomal recessive 11", "Mental Retardation, Autosomal Recessive 11", "mental retardation, autosomal recessive, 11", "intellectual disability, autosomal recessive 11", "autosomal recessive intellectual developmental disorder 11", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 11", "shortest_name_length": 5}
{"curie": "MONDO:0015069", "names": ["anal NET", "Anal NET", "Anal Canal NET", "anal canal NET", "NET of anal canal", "NET of the anal canal", "Anal Neuroendocrine Tumor", "anal Neuroendocrine tumor", "anal canal neuroendocrine tumor", "Anal Canal Neuroendocrine Tumor", "anal canal neuroendocrine neoplasm", "neuroendocrine tumor of anal canal", "Neuroendocrine tumor of anal canal", "Anal Canal Well Differentiated Tumor", "anal canal well differentiated tumor", "neuroendocrine tumor of the anal canal", "neuroendocrine neoplasm of the anal canal", "anal canal well differentiated tumor/carcinoma", "Anal Canal Well Differentiated Tumor/Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuroendocrine tumor of the anal canal", "shortest_name_length": 8}
{"curie": "UMLS:C0235950", "names": ["Zinc low", "low zinc", "Zn++ low", "Zn levels low", "Zinc decreased", "deficiency zinc", "zinc deficiency", "Zinc deficiency", "ZINC DEFICIENCY", "zinc; deficiency", "deficiency; zinc", "deficiencies zinc", "Zinc Deficiency Disorder", "Zinc deficiency (disorder)", "zinc deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Zinc deficiency", "shortest_name_length": 8}
{"curie": "MONDO:0013406", "names": ["ARMD6", "age related macular degeneration 6", "Macular Degeneration, Age-Related, 6", "macular degeneration, age-related, 6", "MACULAR DEGENERATION, AGE-RELATED, 6", "RAX2 age-related macular degeneration", "age related macular degeneration type 6", "macular Degeneration, age-related, type 6", "age-related macular degeneration caused by mutation in RAX2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "age related macular degeneration 6", "shortest_name_length": 5}
{"curie": "MONDO:0019694", "names": ["spondylodysplastic dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondylodysplastic dysplasia", "shortest_name_length": 28}
{"curie": "MONDO:0003316", "names": ["Nonanaplastic Renal Wilms Tumor", "nonanaplastic renal Wilms tumor", "Nonanaplastic Renal Wilms' Tumor", "nonanaplastic renal Wilm's tumor", "nonanaplastic renal Wilms' tumor", "Nonanaplastic Kidney Wilms Tumor", "Nonanaplastic Renal Wilm's Tumor", "nonanaplastic kidney Wilms tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nonanaplastic kidney Wilms tumor", "shortest_name_length": 31}
{"curie": "UMLS:C0280745", "names": ["Secondary MDS", "secondary MDS", "Secondary Myelodysplastic Syndrome", "secondary myelodysplastic syndrome", "secondary myelodysplastic syndromes", "myelodysplastic syndromes, secondary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary Myelodysplastic Syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0015344", "names": ["ATM/TM", "idiopathic acute transverse myelitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic acute transverse myelitis", "shortest_name_length": 6}
{"curie": "UMLS:C3273127", "names": ["Extrahepatic Bile Duct Adenocarcinoma, Gastric Foveolar Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extrahepatic Bile Duct Adenocarcinoma, Gastric Foveolar Type", "shortest_name_length": 60}
{"curie": "MONDO:0020459", "names": ["unstable hemoglobin disease", "Unstable hemoglobin disease", "Unstable haemoglobin disease", "Congenital Heinz body anemia", "Congenital Heinz-body anemia", "Congenital Heinz body anaemia", "Heinz body anemia; congenital", "congenital; anemia, Heinz body", "anemia; congenital, Heinz body", "Unstable hemoglobin disease, NOS", "Unstable haemoglobin disease, NOS", "unstable hemoglobin hemolytic disease", "Unstable hemoglobin hemolytic disease", "Congenital Heinz body hemolytic anemia", "congenital Heinz body hemolytic anemia", "Unstable hemoglobin disease (disorder)", "unstable hemoglobin disease (diagnosis)", "Congenital Heinz body haemolytic anaemia", "CHBHA - Congenital Heinz body hemolytic anemia", "CHBHA - Congenital Heinz body haemolytic anaemia", "congenital Heinz body hemolytic anemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "unstable hemoglobin disease", "shortest_name_length": 27}
{"curie": "UMLS:C4520755", "names": ["Stage I Larynx Epidermoid Carcinoma", "Stage I Epidermoid Carcinoma of Larynx", "Stage I Laryngeal Epidermoid Carcinoma", "Stage I Larynx Squamous Cell Carcinoma", "Stage I Squamous Cell Carcinoma of Larynx", "Stage I Laryngeal Squamous Cell Carcinoma", "Stage I Epidermoid Carcinoma of the Larynx", "Stage I Squamous Cell Carcinoma of the Larynx", "Stage I Laryngeal Throat Squamous Cell Cancer", "Stage I Laryngeal Squamous Cell Carcinoma AJCC v6", "Stage I Laryngeal Squamous Cell Carcinoma AJCC v7", "Stage I Laryngeal Squamous Cell Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Laryngeal Squamous Cell Carcinoma AJCC v6 and v7", "shortest_name_length": 35}
{"curie": "MONDO:0020559", "names": ["O'Sullivan-McLeod syndrome", "O'Sullivan - McLeod syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "O'Sullivan-McLeod syndrome", "shortest_name_length": 26}
{"curie": "UMLS:C5555508", "names": ["Refractory Appendix Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Appendix Adenocarcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0012436", "names": ["NDH", "NDH SYNDROME", "NDH syndrome", "Ndh syndrome", "neonatal diabetes mellitus with congenital hypothyroidism", "Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism", "diabetes mellitus, neonatal, with congenital hypothyroidism", "DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM", "neonatal diabetes-congenital hypothyroidism-congenital glaucoma-hepatic fibrosis-polycystic kidneys syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal diabetes mellitus with congenital hypothyroidism", "shortest_name_length": 3}
{"curie": "MONDO:0005340", "names": ["alopecia areata", "patchy loss of hair", "alopecia circumscripta", "circumscribed alopecia", "Circumscribed alopecia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alopecia areata", "shortest_name_length": 15}
{"curie": "UMLS:C4763661", "names": ["Castration-Resistant Prostate Carcinoma Refractory to Second-Generation ARAT Agents", "Castration-Resistant Prostate Carcinoma Refractory to Second-Generation Androgen Receptor Axis-Targeted Agents"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Castration-Resistant Prostate Carcinoma Refractory to Second-Generation Androgen Receptor Axis-Targeted Agents", "shortest_name_length": 83}
{"curie": "MONDO:0016705", "names": ["ANGL", "angiocentric glioma", "Angiocentric Glioma", "Angiocentric glioma", "Monomorphus Angiocentric Glioma", "Monomorphus angiocentric glioma", "angiocentric glioma (WHO grade I)", "Angiocentric Glioma (WHO Grade I)", "Angiocentric Glioma (WHO Grade 1)", "Angiocentric neurepithelial tumor", "Angiocentric Neuroepithelial Tumor", "angiocentric neuroepithelial tumor", "Angiocentric neuroepithelial tumor", "Angiocentric neuroepithelial tumour", "Angiocentric glioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angiocentric glioma", "shortest_name_length": 4}
{"curie": "MONDO:0011027", "names": ["T2D1", "NIDDM1", "TYPE 2 DIABETES MELLITUS 1", "NONINSULIN-DEPENDENT DIABETES MELLITUS 1", "Noninsulin-Dependent Diabetes Mellitus 1", "noninsulin-dependent diabetes mellitus 1", "diabetes mellitus, noninsulin-dependent 1", "diabetes mellitus, noninsulin-dependent, 1", "Diabetes Mellitus, Noninsulin-Dependent, 1", "DIABETES MELLITUS, NONINSULIN-DEPENDENT, 1", "diabetes mellitus, noninsulin-dependent, type 1", "DIABETES MELLITUS, NONINSULIN-DEPENDENT, 1 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diabetes mellitus, noninsulin-dependent, 1", "shortest_name_length": 4}
{"curie": "MONDO:0003480", "names": ["Pineal Dysgerminoma", "pineal dysgerminoma", "pineal region dysgerminoma", "Pineal Region Dysgerminoma", "pineal body dysgerminoma (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pineal region dysgerminoma", "shortest_name_length": 19}
{"curie": "MONDO:0006846", "names": ["MHT", "Hypertensive emergency", "hypertension malignant", "hypertensive emergency", "Hypertension;malignant", "HYPERTENSIVE EMERGENCY", "HYPERTENSION MALIGNANT", "emergency hypertensive", "Malignant Hypertension", "malignant hypertension", "Malignant hypertension", "Hypertension malignant", "HYPERTENSION, MALIGNANT", "Hypertension, Malignant", "HYPERTENSION ACCELERATED", "emergencies hypertensive", "accelerated hypertension", "Accelerated hypertension", "HYPERTENSION, ACCELERATED", "Malignant hypertension NOS", "malignant phase hypertension", "Hypertensive emergency (disorder)", "Malignant hypertension (disorder)", "accelerated-malignant hypertension", "hypertensive emergency (diagnosis)", "malignant hypertension (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant hypertension", "shortest_name_length": 3}
{"curie": "MONDO:0008096", "names": ["UNNA NEVUS", "Unna Nevus", "Erythema Nuchae", "ERYTHEMA NUCHAE", "erythema nuchae", "nevus flammeus of nape of neck", "NEVUS FLAMMEUS OF NAPE OF NECK", "Nevus Flammeus of Nape of Neck"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nevus flammeus of nape of neck", "shortest_name_length": 10}
{"curie": "MONDO:0056819", "names": ["sinonasal carcinoma", "Sinonasal Carcinoma", "Paranasal sinus and nasal cavity cancer", "Nasal Cavity and Paranasal Sinus Cancer", "nasal cavity and paranasal sinus cancer", "paranasal sinus and nasal cavity cancer", "Nasal Cavity and Paranasal Sinus Carcinoma", "nasal cavity and paranasal sinus carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasal cavity and paranasal sinus carcinoma", "shortest_name_length": 19}
{"curie": "MONDO:0003008", "names": ["Familial Renal Cancer", "familial renal carcinoma", "Familial renal carcinoma", "hereditary renal carcinoma", "hereditary renal cell cancer", "Hereditary Renal Cell Cancer", "renal cell cancer, hereditary", "Familial renal cell carcinoma", "hereditary renal cell carcinoma", "Hereditary Renal Cell Carcinoma", "Familial renal cell carcinoma (disorder)", "hereditary renal cell carcinoma (disease)", "Familial renal cell carcinoma (diagnosis)", "renal malignant carcinoma renal cell familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary renal cell carcinoma", "shortest_name_length": 21}
{"curie": "EFO:1001459", "names": ["diabetic foot"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diabetic foot", "shortest_name_length": 13}
{"curie": "MONDO:0021895", "names": ["TMJ", "TMD", "Costen", "jaw snap", "jaw snaps", "syndrome tmj", "TMJ syndrome", "jaw snapping", "TMJ SYNDROME", "TMJ Syndrome", "Snapping jaw", "tmj syndrome", "Syndrome, TMJ", "costen syndrome", "dysfunction tmj", "Costen; complex", "complex; Costen", "tmj dysfunction", "Costen Syndrome", "costens syndrome", "Costens Syndrome", "Costen's complex", "Costen's Syndrome", "Costen's syndrome", "costen's syndrome", "Syndrome, Costen's", "Clicking jaw syndrome", "Mandibular dysfunction", "mandibular dysfunction", "pain-dysfunction syndrome", "PAIN-DYSFUNCTION SYNDROME", "TMJ-pain-dysfunction syndrome", "TMJ pain dysfunction syndrome", "TEMPO MANDIBULAR JOINT DYSFUNC", "TEMPOROMANDIBULAR JOINT SYNDROME", "Temporomandibular joint syndrome", "temporomandibular joint syndrome", "Temporomandibular Joint Syndrome", "Syndrome, Temporomandibular Joint", "Joint Syndrome, Temporomandibular", "Temporomandibular joint dysfunction", "TEMPOROMANDIBULAR JOINT DYSFUNCTION", "temporomandibular joint dysfunction", "Temporomandibular Joint Dysfunction", "Temporomandibular joint syndrome, NOS", "temporomandibular dysfunction syndrome", "temporomandibular joint dysfunction syndrome", "Temporomandibular Joint Dysfunction Syndrome", "Myofascial pain - dysfunction syndrome of TMJ", "TEMPOROMANDIBULAR JOINT PAIN-DYSFUNCTION SYNDROME", "temporomandibular joint-pain dysfunction syndrome", "TEMPOROMANDIBULAR JOINT-PAIN-DYSFUNCTION SYNDROME", "Temporomandibular joint pain dysfunction syndrome", "Temporomandibular joint-pain-dysfunction syndrome", "syndrome; pain-dysfunction, temporomandibular joint", "pain-dysfunction; syndrome, temporomandibular joint", "TMJPDS - Temporomandibular joint pain dysfunction syndrome", "Temporomandibular joint-pain-dysfunction syndrome (disorder)", "temporomandibular joint-pain dysfunction syndrome (diagnosis)", "Myofascial Pain Dysfunction Syndrome, Temporomandibular Joint"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "temporomandibular joint dysfunction syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0025113", "names": ["poultry disease", "Poultry Disease", "disease poultry", "Poultry Diseases", "Disease, Poultry", "poultry diseases", "disease, poultry", "Poultry--Diseases", "diseases, poultry", "Diseases, Poultry"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "poultry disease", "shortest_name_length": 15}
{"curie": "UMLS:C5231190", "names": ["Accessory Nerve Palsy", "Cranial nerve palsy XI", "Cranial Nerve XI Palsy", "Palsy of accessory nerve", "Eleventh Cranial Nerve Palsy", "Spinal Accessory Nerve Palsy", "Palsy of eleventh cranial nerve", "Palsy of accessory nerve (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Palsy of accessory nerve", "shortest_name_length": 21}
{"curie": "UMLS:C1112155", "names": ["Hereditary non-polyposis colorectal cancer syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hereditary non-polyposis colorectal cancer syndrome", "shortest_name_length": 51}
{"curie": "UMLS:C5446591", "names": ["Allergy, Dairy or Lactose", "Dairy or Lactose Intolerance Allergy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dairy or Lactose Intolerance Allergy", "shortest_name_length": 25}
{"curie": "MONDO:0012994", "names": ["SRD", "DYT-SPR", "SPR DEFICIENCY", "Spr Deficiency", "SPR deficiency", "DRD due to SRD", "Biopterin deficiency", "Sepiapterin reductase deficiency", "Sepiapterin Reductase Deficiency", "sepiapterin reductase deficiency", "SEPIAPTERIN REDUCTASE DEFICIENCY", "7,8-Dihydrobiopterin synthetase deficiency", "Sepiapterin reductase deficiency (disorder)", "autosomal recessive sepiapterin reductase-deficient DRD", "Autosomal recessive sepiapterin reductase-deficient DRD", "Dopa responsive dystonia due to sepiapterin reductase deficiency", "Dopa-responsive dystonia due to sepiapterin reductase deficiency", "Dopa-Responsive Dystonia Due To Sepiapterin Reductase Deficiency", "dopa-responsive dystonia due to sepiapterin reductase deficiency", "Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency", "DYSTONIA, DOPA-RESPONSIVE, DUE TO SEPIAPTERIN REDUCTASE DEFICIENCY", "dystonia, DOPA-responsive, due to sepiapterin reductase deficiency", "Dopa responsive dystonia due to sepiapterin reductase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dopa-responsive dystonia due to sepiapterin reductase deficiency", "shortest_name_length": 3}
{"curie": "MONDO:0006200", "names": ["Epitheliod Cell Uveal Melanoma", "uvea epithelioid cell melanoma", "uveal epithelioid cell melanoma", "Epithelioid Cell Uveal Melanoma", "Uveal Epithelioid Cell Melanoma", "epithelioid cell uveal melanoma", "epithelioid cell melanoma of uvea", "epithelioid cell intraocular melanoma", "intraocular melanoma, epithelioid cell", "melanoma, epithelioid cell intraocular", "melanoma, intraocular, epithelioid cell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epithelioid cell uveal melanoma", "shortest_name_length": 30}
{"curie": "UMLS:C0855078", "names": ["Relapsed Mixed Cellularity Hodgkin's Disease", "Recurrent Mixed Cellularity Hodgkin Lymphoma", "Hodgkin's disease mixed cellularity recurrent", "Relapsed Mixed Cellularity Hodgkin's Lymphoma", "Recurrent Mixed Cellularity Hodgkin's Disease", "Recurrent Mixed Cellularity Hodgkin's Lymphoma", "Recurrent Mixed Cellularity Classic Hodgkin Lymphoma", "Recurrent Mixed Cellularity Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's disease mixed cellularity recurrent", "shortest_name_length": 44}
{"curie": "MONDO:0014157", "names": ["MDPL", "MDP syndrome", "MDPL syndrome", "mandibular hypoplasia-deafness-progeroid syndrome", "mandibular hypoplasia, deafness, progeroid features", "mandibular hypoplasia-hearing loss-progeroid syndrome", "Mandibular hypoplasia-hearing loss-progeroid syndrome", "Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome", "MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME", "mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mandibular hypoplasia-deafness-progeroid syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0001989", "names": ["bald tongue", "Bald tongue", "smooth tongue", "Glazed tongue", "Smooth tongue", "TONGUE GLAZING", "Hunter; glossitis", "glossitis; Hunter", "atrophic glossitis", "Hunter's glossitis", "hunter's glossitis", "glossitis atrophic", "Atrophic glossitis", "Moeller's glossitis", "glossitis, Hunter's", "Glossitis, Hunter's", "glossitis; atrophic", "atrophic; glossitis", "glossitis; moeller's", "Glossitis, Moeller's", "Smooth lingual surface", "Smooth atrophic tongue", "smooth atrophic tongue", "tongue atrophy papillae", "Glossodynia exfoliativa", "Smooth dorsum of tongue", "Tongue Papillary Atrophy", "Smooth surface of tongue", "Atrophy of tongue surface", "tongue; atrophy, papillae", "atrophy; tongue, papillae", "atrophy of tongue papillae", "Atrophy of tongue papillae", "Atrophy of lingual surface", "Tongue denuded of papillae", "Atrophy of dorsum of tongue", "Tongue papillary atrophy NOS", "atrophy of the tongue papillae", "atrophic glossitis (diagnosis)", "Hunter's glossitis (diagnosis)", "Moeller's glossitis (diagnosis)", "Moeller's glossodynia exfoliativa", "Atrophy of tongue papillae (disorder)", "smooth atrophic tongue (physical finding)", "atrophy of the tongue papillae (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrophic glossitis", "shortest_name_length": 11}
{"curie": "UMLS:C0554591", "names": ["idiopathic polymyositis", "Idiopathic Polymyositis", "Idiopathic polymyositis", "Polymyositis, Idiopathic", "Idiopathic Polymyositides", "Polymyositides, Idiopathic", "Idiopathic polymyositis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Polymyositis, Idiopathic", "shortest_name_length": 23}
{"curie": "MONDO:0014067", "names": ["MRT35", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 35", "mental retardation, autosomal recessive 35", "intellectual disability, autosomal recessive 35", "autosomal recessive intellectual developmental disorder 35", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 35", "short ulna-dysmorphism-hypotonia-intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short ulna-dysmorphism-hypotonia-intellectual disability syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0044737", "names": ["SPG81", "hereditary spastic paraplegia 81", "spastic paraplegia 81 autosomal recessive", "autosomal recessive complex SPG due to Kennedy pathway dysfunction", "autosomal recessive complex spastic paraplegia due to kennedy pathway dysfunction", "autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive complex spastic paraplegia due to kennedy pathway dysfunction", "shortest_name_length": 5}
{"curie": "MONDO:0017167", "names": ["malignant epithelial tumor of salivary glands", "malignant epithelial tumor of the salivary glands"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant epithelial tumor of salivary glands", "shortest_name_length": 45}
{"curie": "MONDO:0033123", "names": ["EVR7", "EXUDATIVE VITREORETINOPATHY 7", "exudative vitreoretinopathy 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exudative vitreoretinopathy 7", "shortest_name_length": 4}
{"curie": "MONDO:0018206", "names": ["childhood-onset autosomal recessive myopathy with external ophthalmoplegia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood-onset autosomal recessive myopathy with external ophthalmoplegia", "shortest_name_length": 74}
{"curie": "MONDO:0012748", "names": ["CILD7", "Cild7", "primary ciliary dyskinesia 7", "CILIARY DYSKINESIA, PRIMARY, 7", "ciliary dyskinesia, primary, 7", "Ciliary Dyskinesia, Primary, 7", "primary ciliary dyskinesia type 7", "DNAH11 primary ciliary dyskinesia", "ciliary dyskinesia, primary, type 7", "primary ciliary dyskinesia caused by mutation in DNAH11", "primary ciliary dyskinesia 7 with or without situs inversus", "Ciliary Dyskinesia, Primary, 7, With Or Without Situs Inversus", "ciliary dyskinesia, primary, 7, with or without situs inversus", "CILIARY DYSKINESIA, PRIMARY, 7, WITH OR WITHOUT SITUS INVERSUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia 7", "shortest_name_length": 5}
{"curie": "MONDO:0034103", "names": ["infection-related hemolytic uremic syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infection-related hemolytic uremic syndrome", "shortest_name_length": 43}
{"curie": "MONDO:0004890", "names": ["Circinate choroidal dystrophy", "circinate choroidal dystrophy", "Choroidal dystrophy, circinate", "Partial central choroid dystrophy", "partial central choroid dystrophy", "partial central choroidal dystrophy", "partial central dystrophy of choroid", "Partial central dystrophy of choroid", "Choroidal dystrophy, central areolar", "choroidal dystrophy, central areolar", "Central dystrophy of choroid, partial", "circinate choroidal dystrophy (diagnosis)", "Partial central choroid dystrophy (disorder)", "partial central hereditary choroidal dystrophy", "partial central choroidal dystrophy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial central choroid dystrophy", "shortest_name_length": 29}
{"curie": "MONDO:0010535", "names": ["BZX", "BDCS", "Bazex syndrome", "BAZEX SYNDROME", "bazex syndrome", "acrokeratosis of Bazex", "Acrokeratosis of Bazex", "Bazex-Dupre-Christol syndrome", "Bazex-Dupré-Christol syndrome", "acrokeratosis paraneoplastica", "Acrokeratosis paraneoplastica", "BAZEX-DUPRE-CHRISTOL SYNDROME", "Bazex syndrome, X-linked dominant", "Bazex syndrome - acquired keratoderma", "Acrokeratosis paraneoplastica of Bazex", "acrokeratosis paraneoplastica of Bazex", "follicular atrophoderma and basal cell carcinomas", "FOLLICULAR ATROPHODERMA AND BASAL CELL CARCINOMAS", "Acrokeratosis paraneoplastica of Bazex (disorder)", "Follicular atrophoderma and basal cell carcinomas", "Follicular atrophoderma and basal cell epitheliomata", "Follicular atrophoderma-basal cell carcinoma syndrome", "follicular atrophoderma-basal cell carcinoma syndrome", "Follicular atrophoderma and basal cell epitheliomata (disorder)", "Follicular atrophoderma and basal cell epitheliomata (diagnosis)", "Follicular atrophoderma-basocellular proliferations-hypotrichosis syndrome", "follicular atrophoderma-basocellular proliferations-hypotrichosis syndrome", "skin neoplasm malignant follicular atrophoderma and basal cell epitheliomata"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bazex-Dupre-Christol syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0016591", "names": ["SAOA", "idiopathic late-onset cerebellar ataxia", "Idiopathic late-onset cerebellar ataxia", "Sporadic adult-onset ataxia of unknown origin", "sporadic adult-onset ataxia of unknown etiology", "Sporadic adult-onset ataxia of unknown etiology", "Sporadic adult-onset ataxia of unknown aetiology", "Sporadic adult-onset ataxia of unknown etiology (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sporadic adult-onset ataxia of unknown etiology", "shortest_name_length": 4}
{"curie": "UMLS:C3640088", "names": ["Heterotaxy, Asplenia", "Heterotaxy Syndrome with Asplenia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Heterotaxy Syndrome with Asplenia", "shortest_name_length": 20}
{"curie": "UMLS:C1332928", "names": ["Chest Wall Disease", "Chest Wall Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chest Wall Disorder", "shortest_name_length": 18}
{"curie": "MONDO:0024525", "names": ["FRTS1", "adult Fanconi syndrome", "renal Fanconi syndrome", "Luder-Sheldon syndrome", "Fanconi renotubular syndrome", "DeToni-Debré-Fanconi syndrome", "FANCONI RENOTUBULAR SYNDROME 1", "Fanconi renotubular syndrome 1", "primary Fanconi renal syndrome", "Fanconi syndrome without cystinosis", "primary Fanconi renotubular syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fanconi renotubular syndrome 1", "shortest_name_length": 5}
{"curie": "MONDO:0700190", "names": ["Chicken Bursal Lymphoma", "chicken bursal lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chicken bursal lymphoma", "shortest_name_length": 23}
{"curie": "MONDO:0008208", "names": ["Patella, Familial Recurrent Dislocation Of", "PATELLA, FAMILIAL RECURRENT DISLOCATION OF", "patella, familial recurrent dislocation of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "patella, familial recurrent dislocation of", "shortest_name_length": 42}
{"curie": "MONDO:0003928", "names": ["uterine myxoid leiomyosarcoma", "uterine corpus myxoid leiomyosarcoma", "body of uterus myxoid leiomyosarcoma", "Uterine Corpus Myxoid Leiomyosarcoma", "myxoid leiomyosarcoma of body of uterus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine corpus myxoid leiomyosarcoma", "shortest_name_length": 29}
{"curie": "MONDO:0015061", "names": ["NTOS", "Neurogenic TOS", "neurogenic TOS", "neurogenic cervical rib syndrome", "Neurogenic cervical rib syndrome", "neurogenic thoracic outlet syndrome", "Neurogenic Thoracic Outlet Syndrome", "Neurogenic costoclavicular syndrome", "neurogenic costoclavicular syndrome", "Neurogenic thoracic outlet syndrome", "Thoracic Outlet Syndrome, Neurogenic", "Neurogenic thoracic outlet syndrome (disorder)", "Neurogenic thoracic outlet compression syndrome", "neurogenic thoracic outlet compression syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurogenic thoracic outlet syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0017343", "names": ["EBV Lymphoproliferation", "EBV-Related Lymphoproliferative Disorder", "EBV-associated lymphoproliferative disorder", "Epstein-Barr Virus-Related Lymphoproliferative Disorder", "Epstein-Barr Virus-Associated Lymphoproliferative Disorder", "Epstein-Barr virus associated lymphoproliferative disorder", "Epstein-Barr virus-associated malignant lymphoproliferative disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epstein-Barr virus-associated malignant lymphoproliferative disorder", "shortest_name_length": 23}
{"curie": "UMLS:C2007070", "names": ["Gallbladder Carcinosarcoma", "carcinosarcoma of gallbladder", "carcinosarcoma of gallbladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinosarcoma of gallbladder", "shortest_name_length": 26}
{"curie": "MONDO:0006633", "names": ["acalculous cholecystitis", "Acalculous cholecystitis", "cholecystitis acalculous", "Acalculous Cholecystitis", "Cholecystitis, Acalculous", "Acute acalculous cholecystitis", "cholecystitis without calculus", "Cholecystitis without calculus", "acute acalculous cholecystitis", "Acute Acalculous Cholecystitis", "Cholecystitis, NOS without calculus", "Acalculous Gallbladder Inflammation", "Acute cholecystitis without calculus", "acalculous cholecystitis (diagnosis)", "acute cholecystitis without calculus", "Gallbladder Inflammation, Acalculous", "Cholecystitis without calculus (disorder)", "Acute cholecystitis without calculus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acalculous cholecystitis", "shortest_name_length": 24}
{"curie": "MONDO:0004401", "names": ["refractory testis cancer", "testis refractory cancer", "testis cancer, refractory", "refractory cancer of testis", "Refractory Cancer of Testis", "Refractory Testicular Cancer", "refractory testicular cancer", "testicular cancer, refractory", "refractory testicular carcinoma", "Refractory Cancer of the Testis", "refractory cancer of the testis", "Refractory testicular carcinoma", "cancer of the testis, refractory", "refractory carcinoma of the testis", "carcinoma of the testis, refractory", "refractory malignant testicular germ cell tumor", "Refractory Malignant Testicular Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testis refractory cancer", "shortest_name_length": 24}
{"curie": "UMLS:C1333773", "names": ["Gastric Hodgkin Lymphoma", "Gastric Hodgkin's Disease", "Gastric Hodgkin's Lymphoma", "Hodgkin's lymphoma of stomach", "Hodgkin's Lymphoma of Stomach", "Primary Gastric Hodgkin Lymphoma", "Hodgkin's Lymphoma of the Stomach", "Primary Gastric Hodgkin's Lymphoma", "Hodgkin's lymphoma of stomach (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Hodgkin's Lymphoma", "shortest_name_length": 24}
{"curie": "MONDO:0006369", "names": ["PPTID", "Pineal parenchymal tumor of intermediate differenciation", "pineal parenchymal tumor of intermediate differentiation", "Pineal parenchymal tumor of intermediate differentiation", "Pineal Parenchymal Tumor of Intermediate Differentiation", "pineal parenchymal tumors of intermediate differentiation", "Pineal parenchymal tumour of intermediate differentiation", "pineal parenchymal tumour of intermediate differentiation", "Pineal parenchymal tumor of intermediate differentiation (disorder)", "pineal parenchymal tumor of intermediate differentiation (diagnosis)", "pineal parenchymal tumor of intermediate differentiation (morphologic abnormality)", "Pineal parenchymal tumor of intermediate differentiation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pineal parenchymal tumor of intermediate differentiation", "shortest_name_length": 5}
{"curie": "UMLS:C0457521", "names": ["Unicystic ameloblastoma", "Unicystic Ameloblastoma", "Cystogenic Ameloblastoma", "Ameloblastoma, Unicystic Type", "Unicystic ameloblastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unicystic ameloblastoma", "shortest_name_length": 23}
{"curie": "MONDO:0010041", "names": ["SACS", "sacs", "SPAX6", "ARSACS", "Spastic Ataxia 6", "Charlevoix-Saguenay spastic ataxia", "CHARLEVOIX-SAGUENAY SPASTIC ATAXIA", "Spastic ataxia 6, autosomal recessive", "Spastic ataxia of Charlevoix-Saguenay", "SPASTIC ATAXIA 6, AUTOSOMAL RECESSIVE", "spastic ataxia 6, autosomal recessive", "spastic ataxia of Charlevoix-Saguenay", "Spastic ataxia Charlevoix-Saguenay type", "spastic ataxia Charlevoix-Saguenay type", "Spastic Ataxia, Charlevoix-Saguenay Type", "spastic ataxia, Charlevoix-Saguenay type", "SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE", "autosomal recessive spastic ataxia type 6", "Autosomal recessive spastic ataxia type 6", "Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay", "autosomal recessive spastic ataxia of Charlevoix-Saguenay", "Autosomal recessive spastic ataxia of Charlevoix-Saguenay", "AUTOSOMAL RECESSIVE SPASTIC ATAXIA OF CHARLEVOIX-SAGUENAY", "ARSACS - autosomal recessive spastic ataxia of Charlevoix-Saguenay", "Autosomal recessive spastic ataxia of Charlevoix-Saguenay (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charlevoix-Saguenay spastic ataxia", "shortest_name_length": 4}
{"curie": "MONDO:0000428", "names": ["Y-linked disease", "disease, Y-linked", "Y-linked genetic disease", "Y-Linked Genetic Disease", "Disease, Y-Linked Genetic", "Y Linked Genetic Diseases", "Genetic Disease, Y-Linked", "genetic disease, Y-linked", "disease, Y-linked genetic", "Y-Linked Genetic Diseases", "Y linked genetic diseases", "Y-linked genetic diseases", "Diseases, Y-Linked Genetic", "diseases, Y-linked genetic", "Y-linked monogenic disease", "genetic diseases, Y linked", "Genetic Diseases, Y-Linked", "Genetic Diseases, Y Linked", "Y-linked disease or disorder", "disease or disorder, Y-linked", "Genetic Diseases, Y-Chromosome Linked", "genetic diseases, Y-chromosome linked", "Genetic Diseases, Y Chromosome Linked", "genetic diseases, Y chromosome linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Y-linked disease", "shortest_name_length": 16}
{"curie": "UMLS:C0026635", "names": ["mouth breath", "Jaw breathing", "breathing mouth", "MOUTH BREATHING", "Mouth Breathing", "mouth breathing", "Mouth breathing", "Breathing orally", "Breathing, Mouth", "Mouth Breathings", "Breathings, Mouth", "respiration; mouth", "mouth; respiratory", "Open mouth breathing", "mouth breathing was seen", "Mouth breathing (finding)", "mouth breathing (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mouth Breathing", "shortest_name_length": 12}
{"curie": "MONDO:0100354", "names": ["MMIHS", "MMIHS1", "MMIH Syndrome", "MMIH syndrome", "Berdon syndrome", "BERDON SYNDROME", "Berdon's syndrome", "visceral myopathy", "Megacystis, microcolon, hypoperistalsis syndrome", "Megacystis, Microcolon, Hypoperistalsis Syndrome", "megacystis, microcolon, hypoperistalsis syndrome", "Megacystis microcolon intestinal hypoperistalsis syndrome", "MEGACYSTIS-MICROCOLON-INTESTINAL HYPOPERISTALSIS SYNDROME", "megacystis microcolon intestinal hypoperistalsis syndrome", "Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome", "Megacystis-microcolon-intestinal hypoperistalsis syndrome", "megacystis-microcolon-intestinal hypoperistalsis syndrome", "megacystis, microcolon, intestinal hypoperistalsis syndrome", "megacystis-microcolon-intestinal hypoperistalsis syndrome 1", "MEGACYSTIS-MICROCOLON-INTESTINAL HYPOPERISTALSIS SYNDROME 1", "Megacystis, Microcolon, Intestinal Hypoperistalsis Syndrome", "Megacystis, microcolon, hypoperistalsis syndrome (disorder)", "megacystis-microcolon-intestinal hypoperistalsis syndrome, MMIH", "MMIHS Megacystis microcolon intestinal hypoperistalsis syndrome", "megacystis-microcolon-intestinal hypoperistalsis-hydronephrosis syndrome", "Megacystis-microcolon-intestinal hypoperistalsis-hydronephrosis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "megacystis-microcolon-intestinal hypoperistalsis syndrome 1", "shortest_name_length": 5}
{"curie": "MONDO:0013785", "names": ["MRT34", "Mental Retardation, Autosomal Recessive 34", "mental retardation, autosomal recessive 34", "mental retardation, autosomal recessive type 34", "intellectual disability, autosomal recessive 34", "intellectual disability, autosomal recessive type 34", "autosomal recessive intellectual developmental disorder 34", "CRADD autosomal recessive non-syndromic intellectual disability", "mental retardation, autosomal recessive 34, with variant lissencephaly", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 34, WITH VARIANT LISSENCEPHALY", "Mental Retardation, Autosomal Recessive 34, with Variant Lissencephaly", "intellectual disability, autosomal recessive 34, with variant lissencephaly", "autosomal recessive non-syndromic intellectual disability caused by mutation in CRADD", "intellectual developmental disorder, autosomal recessive 34, with variant lissencephaly", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 34, WITH VARIANT LISSENCEPHALY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 34", "shortest_name_length": 5}
{"curie": "UMLS:C2825772", "names": ["Benign Leiomyoblastoma", "Benign Epithelioid Cell Type Gastrointestinal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Epithelioid Cell Type Gastrointestinal Stromal Tumor", "shortest_name_length": 22}
{"curie": "MONDO:0001531", "names": ["CLOTTING", "Coagulopathy", "COAGULOPATHY", "coagulopathy", "coagulopathies", "Coagulopathies", "clotting disorder", "bleeding disorder", "Clotting disorder", "Coagulopathy, NOS", "bleeding tendency", "bleeding disorders", "bleeding diathesis", "Bleeding disorders", "Clotting disorders", "COAGULATION DEFECT", "Coagulation Defect", "coagulation defect", "clotting disorders", "Hemostatic disorder", "coagulation defects", "hemostatic disorder", "Coagulation defects", "disorder; hemostasis", "DISORDER COAGULATION", "Coagulation Disorder", "Disorder coagulation", "Disorder, hemostasis", "coagulation disorder", "COAGULATION DISORDER", "Coagulation disorder", "Abnormal;coagulation", "abnormal coagulation", "Coagulation Disorders", "Disorder, coagulation", "coagulation disorders", "Coagulopathy, specify", "Disorder of hemostasis", "Blood clotting disorder", "blood clotting disorder", "Disorder of haemostasis", "Defect coagulation (NOS)", "blood clotting disorders", "BLOOD COAGULATION DEFECT", "disorder; blood clotting", "Coagulation disorder NOS", "DEFECT COAGULATION (NOS)", "blood clotting; disorder", "disorders of coagulation", "blood coagulation disease", "Coagulation, Disorders of", "Defective coagulation NOS", "Coagulation disorder, NOS", "blood coagulation disorder", "BLOOD COAGULATION DISORDER", "Blood Coagulation Disorder", "Blood coagulation disorder", "COAGULATION DISORDER (NOS)", "coagulation disorder, blood", "Disorder of hemostasis, NOS", "Disorder, Blood Coagulation", "Blood coagulation disorders", "Blood Coagulation Disorders", "blood coagulation disorders", "disorder, blood coagulation", "coagulation protein disease", "disturbance; blood clotting", "Coagulation Disorder, Blood", "Blood clotting disorder, NOS", "disorders, blood coagulation", "Disorders, Blood Coagulation", "Coagulation Disorders, Blood", "coagulation disorders, blood", "Disorder of haemostasis, NOS", "Disorder of hemostatic system", "disorder of hemostatic system", "postpartum coagulation defect", "Hemostatic function, abnormal", "DISORDERS OF BLOOD COAGULATION", "Disorder of haemostatic system", "Blood coagulation disorder, NOS", "Coagulation defect, unspecified", "coagulation defects (diagnosis)", "inherited blood coagulation disease", "Blood coagulation disorder (disorder)", "blood coagulation disorder (diagnosis)", "Abnormality of the coagulation cascade", "Disorder of hemostatic system (disorder)", "disorder of hemostatic system (diagnosis)", "postpartum coagulation defect with delivery", "Blood coagulation disorder, disease or syndrome", "DISORDERS OF BLOOD COAGULATION: GENERAL CONDITIONS", "Blood Coagulation Disorders, Diseases and Syndromes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blood coagulation disease", "shortest_name_length": 8}
{"curie": "MONDO:0018068", "names": ["Patau", "D1 Trisomy", "trisomy 13", "D1 trisomy", "13 trisomy", "Trisomy 13", "trisomy; 13", "13 trisomies", "Patau Syndrome", "syndrome patau", "patau syndrome", "Patau syndrome", "Pataus Syndrome", "trisomy type 13", "Patau's Syndrome", "patau's syndrome", "Patau's syndrome", "Trisomy 13 Syndrome", "trisomy syndrome 13", "trisomy 13 syndrome", "Trisomy 13 syndrome", "D1 trisomy syndrome", "Trisomy 13 Syndromes", "D>1< trisomy syndrome", "trisomy; syndrome, 13", "syndrome; trisomy, 13", "trisomy 13 (diagnosis)", "Trisomy 13, unspecified", "chromosome; 13, trisomy", "Bartholin Patau Syndrome", "Bartholin-Patau syndrome", "Bartholin-Patau Syndrome", "Complete Trisomy 13 Syndrome", "Complete trisomy 13 syndrome", "D trisomy syndrome (formerly)", "Patau's syndrome, unspecified", "chromosome 13 trisomy syndrome", "D<sub>1</sub> trisomy syndrome", "Chromosome 13 Trisomy Syndrome", "[OBSOLETE] Trisomy 13 syndrome", "chromosome 13, trisomy 13 complete", "Complete trisomy 13 syndrome (disorder)", "Chromosomal imbalance syndrome, pair 13, trisomy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trisomy 13", "shortest_name_length": 5}
{"curie": "MONDO:0015846", "names": ["syndromic uterovaginal malformation", "syndrome associated with uterovaginal malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic uterovaginal malformation", "shortest_name_length": 35}
{"curie": "MONDO:0021752", "names": ["Achard Thiers syndrome", "Achard-Thiers syndrome", "Diabetes in bearded women", "diabetes in bearded women", "Bearded female with diabetes", "Diabetic-bearded women syndrome", "Diabetic-bearded woman syndrome", "diabetic-bearded woman syndrome", "Achard-Thiers syndrome (disorder)", "Achard-Thiers syndrome (diagnosis)", "Adenoma associated virilism of older women"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Achard-Thiers syndrome", "shortest_name_length": 22}
{"curie": "MONDO:0032774", "names": ["COFG", "cerebellar, ocular, craniofacial, and genital syndrome", "CEREBELLAR, OCULAR, CRANIOFACIAL, AND GENITAL SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellar, ocular, craniofacial, and genital syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0030061", "names": ["PVNH9", "PERIVENTRICULAR NODULAR HETEROTOPIA 9", "periventricular nodular heterotopia 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "periventricular nodular heterotopia 9", "shortest_name_length": 5}
{"curie": "MONDO:0002715", "names": ["Uterus Cancer", "uterine tumor", "uterus cancer", "UTERINE CANCER", "uterine cancer", "Uterine Cancer", "Uterus--Cancer", "Uterus Cancers", "Cancer, Uterus", "Uterine cancer", "uterine cancers", "Cancer, Uterine", "Uterine Cancers", "Cancers, Uterus", "uterus neoplasm", "Tumour of uterus", "Cancer of uterus", "tumour of uterus", "Cancers, Uterine", "Cancer of Uterus", "cancer of uterus", "Uterine Neoplasms", "neoplasm of uterus", "Uterine cancer NOS", "Uterine cancer, NOS", "cancer of the uterus", "Cancer of the Uterus", "CA - cancer of uterus", "Neoplasm malig;uterus", "CA - Cancer of uterus", "Malignant Uterine Tumor", "malignant uterine tumor", "Malignant Tumor of Uterus", "malignant tumor of uterus", "Malignant tumor of uterus", "malignant uterus neoplasm", "Malignant Uterine Neoplasm", "Malignant tumour of uterus", "malignant uterine neoplasm", "uterine cancer (diagnosis)", "Malignant neoplasm of uterus", "malignant neoplasm of uterus", "Malignant Neoplasm of Uterus", "malignant tumor of the uterus", "Malignant Tumor of the Uterus", "Malignant Neoplasm of the Uterus", "malignant neoplasm of the uterus", "malignant neosplasm of the uterus", "Malignant neoplasm of uterus, NOS", "Malignant neoplasm of uterus (disorder)", "malignant neoplasm of uterus (diagnosis)", "Malignant neoplasm of uterus, part unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine cancer", "shortest_name_length": 13}
{"curie": "MONDO:0009491", "names": ["HMS", "Haim-Munk syndrome", "HAIM-Munk syndrome", "HAIM-MUNK SYNDROME", "Haim Munk syndrome", "COCHIN JEWISH DISORDER", "Cochin Jewish disorder", "Haim Munk syndrome (disorder)", "keratosis palmoplantaris with periodontopathia and onychogryposis", "KERATOSIS PALMOPLANTARIS WITH PERIODONTOPATHIA AND ONYCHOGRYPOSIS", "Keratosis palmoplantaris-periodontopathia-onychogryposis syndrome", "Palmoplantar keratoderma-periodontopathia-onychogryposis syndrome", "Keratosis palmoplantaris with periodontopathia and onychogryposis", "palmoplantar keratoderma-periodontopathia-onychogryposis syndrome", "keratosis palmoplantaris-periodontopathia-onychogryposis syndrome", "Palmoplantar hyperkeratosis-periodontopathia-onychogryposis syndrome", "palmoplantar hyperkeratosis-periodontopathia-onychogryposis syndrome", "Keratosis palmoplantaris with periodontopathia and onychogryposis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Haim-Munk syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0004117", "names": ["ampullary small cell carcinoma", "Ampullary Small Cell Carcinoma", "Ampulla of Vater Small Cell NEC", "ampulla of Vater small cell NEC", "ampulla of Vater small cell carcinoma", "Ampulla of Vater Small Cell Carcinoma", "hepatopancreatic ampulla small cell carcinoma", "ampulla of vater small cell neuroendocrine carcinoma", "Ampulla of Vater Small Cell Neuroendocrine Carcinoma", "ampulla of Vater small cell neuroendocrine carcinoma", "small cell neuroendocrine carcinoma of the ampullary region", "Small Cell Neuroendocrine Carcinoma of the Ampullary Region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ampulla of vater small cell neuroendocrine carcinoma", "shortest_name_length": 30}
{"curie": "UMLS:C0237979", "names": ["Toxic amblyopia", "amblyopia toxic", "toxic amblyopia", "AMBLYOPIA, TOXIC", "toxic; amblyopia", "amblyopia; toxic", "Toxic amblyopia (disorder)", "Toxic amblyopia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Toxic amblyopia", "shortest_name_length": 15}
{"curie": "UMLS:C1832033", "names": ["Subependymal Giant Cell Astrocytoma", "adult subependymal giant cell astrocytoma", "Adult Subependymal Giant Cell Astrocytoma", "astrocytoma, adult subependymal giant cell", "subependymal giant cell astrocytoma, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Subependymal Giant Cell Astrocytoma", "shortest_name_length": 35}
{"curie": "UMLS:C1709573", "names": ["Pleural Epithelioid Hemangioendothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pleural Epithelioid Hemangioendothelioma", "shortest_name_length": 40}
{"curie": "MONDO:0011771", "names": ["HMN3", "HMN4", "HMN 4", "HMN 3", "DSMA3", "DHMN3", "dHMN3", "dSMA3", "dHMN4", "DHMN4", "HMN IV", "HMN III", "dHMN3 and dHMN4", "Distal spinal muscular atrophy type 3", "distal spinal muscular atrophy type 3", "neuropathy, distal hereditary motor, type 4", "Neuropathy, Distal Hereditary Motor, Type IV", "NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IV", "neuronopathy, distal hereditary motor, type 3", "neuronopathy, distal hereditary motor, type 4", "NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IV", "Neuronopathy, Distal Hereditary Motor, Type IV", "Neuronopathy, Distal Hereditary Motor, Type III", "NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE III", "distal hereditary motor neuropathy type 3 and type 4", "Distal hereditary motor neuropathy type 3 and type 4", "Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3", "SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 3", "spinal muscular atrophy, distal, autosomal recessive, 3", "autosomal recessive distal spinal muscular atrophy type 3", "Autosomal recessive distal spinal muscular atrophy type 3", "spinal muscular atrophy, chronic distal, autosomal recessive", "Autosomal recessive distal spinal muscular atrophy type 3 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal spinal muscular atrophy type 3", "shortest_name_length": 4}
{"curie": "UMLS:C0159765", "names": ["Open fracture of wrist, NOS", "Open Fracture of Carpal Bone", "Open fracture of carpal bone", "open fracture of carpal bone", "Open fractures of carpal bones", "Open fracture of carpal bone, NOS", "Open fracture of carpal bone of wrist", "Open fracture of carpal bone (disorder)", "open fracture of carpal bone (diagnosis)", "Open fracture of carpal bone, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Open fracture of carpal bone, unspecified", "shortest_name_length": 27}
{"curie": "UMLS:C1336340", "names": ["stage IVA hypopharyngeal cancer", "Stage IVA Hypopharynx Carcinoma", "Stage IVA Carcinoma of Hypopharynx", "Stage IVA Hypopharyngeal Carcinoma", "Stage IVA Carcinoma of the Hypopharynx", "Stage IVA Hypopharyngeal Throat Cancer", "Stage IVA Hypopharyngeal Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Hypopharyngeal Carcinoma AJCC v7", "shortest_name_length": 31}
{"curie": "UMLS:C0157987", "names": ["allergic arthritis", "Arthritis;allergic", "Allergic arthritis", "Arthritis allergic", "Allergic Arthritis", "arthritis allergic", "allergic; arthritis", "arthritis; allergic", "Arthritis allergic NOS", "Allergic arthritis (disorder)", "allergic arthritis (diagnosis)", "Allergic arthritis, site unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Allergic arthritis", "shortest_name_length": 18}
{"curie": "UMLS:C1516410", "names": ["Cervical Blue Nevus", "Blue Nevus of the Cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Blue Nevus", "shortest_name_length": 19}
{"curie": "MONDO:0006521", "names": ["Rash acneiform", "Acneiform Dermatitis", "Dermatitis acneiform", "Acneiform dermatitis", "ACNEIFORM DERMATITIS", "acneiform dermatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acneiform dermatitis", "shortest_name_length": 14}
{"curie": "MONDO:0021175", "names": ["Herpetic vulvovaginitis", "Herpetic Vulvovaginitis", "herpetic vulvovaginitis", "Herpetic vulvovaginitis (disorder)", "herpetic vulvovaginitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "herpetic vulvovaginitis", "shortest_name_length": 23}
{"curie": "MONDO:0016883", "names": ["del(1p)", "1p deletion", "deletion 1p", "1p monosomy", "Deletion 1p", "monosomy 1p", "Monosomy 1p", "1p- syndrome", "del(1p) syndrome", "partial monosomy 1p", "1p partial monosomy", "deletion 1p syndrome", "1p deletion syndrome", "loss of chromosome 1p", "chromosome 1p deletion", "chromosome 1p monosomy", "Chromosome 1, monosomy 1p", "1p partial monosomy syndrome", "1p partial monosomy (disorder)", "chromosome 1p deletion syndrome", "1p chromosome deletion syndrome", "Partial deletion of chromosome 1p", "partial monosomy of chromosome 1p", "partial deletion of chromosome 1p", "Partial monosomy of chromosome 1p", "1p partial monosomy syndrome (diagnosis)", "Partial monosomy of the short arm of chromosome 1", "Partial deletion of the short arm of chromosome 1", "partial deletion of the short arm of chromosome 1", "partial monosomy of the short arm of chromosome 1", "partial deletion of the short arm of chromosome type 1", "anomaly of chromosome pair 1p partial monosomy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of the short arm of chromosome 1", "shortest_name_length": 7}
{"curie": "UMLS:C4521620", "names": ["Stage IV Bone Cancer", "Stage IV Bone Cancer AJCC v8", "Stage IV Appendicular Skeleton, Trunk, Skull, and Facial Bones Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Bone Cancer AJCC v8", "shortest_name_length": 20}
{"curie": "MONDO:0021351", "names": ["Neck Tumor", "neck tumor", "tumor neck", "NECK TUMOR", "neck tumors", "neck tumour", "Neck--Tumors", "tumor of neck", "Tumor of neck", "neoplasm neck", "neck neoplasm", "Neck Neoplasm", "Tumor of Neck", "Tumour of neck", "Neoplasm, Neck", "Neck Neoplasms", "Neoplasms, Neck", "neoplasm of neck", "Neoplasm of Neck", "Neoplasm of neck", "Tumor of the Neck", "tumor of the neck", "neoplasm of the neck", "Neoplasm of the Neck", "neck neoplasm (disease)", "Neoplasm of neck (disorder)", "neoplasm of neck (diagnosis)", "Neck Neoplasms (Including All Pharyngeal Related Neoplasms)", "neck neoplasms (Including All pharyngeal related neoplasms)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplasm of neck", "shortest_name_length": 10}
{"curie": "MONDO:0007789", "names": ["HYPERTROPHIA MUSCULORUM VERA", "Hypertrophia Musculorum Vera", "hypertrophia musculorum vera"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophia musculorum vera", "shortest_name_length": 28}
{"curie": "MONDO:0021491", "names": ["benign gum tumor", "Benign Gum Tumor", "benign tumor of gum", "Benign Tumor of Gum", "Benign Gum Neoplasm", "Benign tumor of gum", "benign gum neoplasm", "Benign tumour of gum", "Benign Gingival Tumor", "benign gingival tumor", "Benign neoplasm of gum", "Benign Neoplasm of Gum", "benign neoplasm of gum", "Benign Tumor of the Gum", "benign tumor of gingiva", "Benign tumor of gingiva", "benign tumor of the gum", "Benign Tumor of Gingiva", "gingiva benign neoplasm", "Benign Gingival Neoplasm", "benign gingival neoplasm", "Benign tumour of gingiva", "Benign neoplasm of the gum", "benign neoplasm of gingiva", "Benign Neoplasm of the Gum", "benign neoplasm of the gum", "Benign Neoplasm of Gingiva", "Benign neoplasm of gum, NOS", "Benign Tumor of the Gingiva", "benign tumor of the gingiva", "benign neoplasm of the gingiva", "Benign Neoplasm of the Gingiva", "Benign neoplasm of the gingiva", "Benign tumor of alveolar mucosa", "Benign tumour of alveolar mucosa", "Benign neoplasm of gum (disorder)", "benign neoplasm of gingiva (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of gum", "shortest_name_length": 16}
{"curie": "MONDO:0000496", "names": ["Cystitis hemorrhagic", "Hemorrhagic Cystitis", "hemorrhagic cystitis", "CYSTITIS HEMORRHAGIC", "Hemorrhagic cystitis", "cystitis hemorrhagic", "HEMORRHAGIC CYSTITIS", "Haemorrhagic cystitis", "haemorrhagic cystitis", "CYSTITIS HAEMORRHAGIC", "Cystitis haemorrhagic", "Hemorrhagic cystitis (disorder)", "Hemorrhagic cystitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemorrhagic cystitis", "shortest_name_length": 20}
{"curie": "MONDO:0009034", "names": ["BLSS", "Craniofacial dyssynostosis", "craniofacial dyssynostosis", "Bilateral lambdoid and sagittal synostosis", "bilateral lambdoid and sagittal synostosis", "BILATERAL LAMBDOID AND SAGITTAL SYNOSTOSIS", "craniofacial dyssynostosis and short stature", "Craniofacial dyssynostosis and short stature", "Craniofacial Dyssynostosis with Short Stature", "craniofacial dyssynostosis with short stature", "CRANIOFACIAL DYSSYNOSTOSIS WITH SHORT STATURE", "Isolated sagittal and bilambdoid craniosynostosis", "craniosynostosis-craniofacial dysostosis syndrome", "Craniosynostosis-craniofacial dysostosis syndrome", "Non-syndromic bilambdoid and sagittal craniosynostosis", "Non-syndromic sagittal and bilateral lambdoid synostosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniofacial dyssynostosis", "shortest_name_length": 4}
{"curie": "UMLS:C4725682", "names": ["Platinum-Resistant Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Platinum-Resistant Urothelial Carcinoma", "shortest_name_length": 39}
{"curie": "UMLS:C3495144", "names": ["Articulatory Apraxia", "Apraxia, Articulatory", "Articulatory Apraxias", "Articulatory Dyspraxia", "Apraxias, Articulatory", "Dyspraxia, Articulatory", "Articulatory Dyspraxias", "Dyspraxias, Articulatory"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Apraxia, Articulatory", "shortest_name_length": 20}
{"curie": "UMLS:C2981258", "names": ["Stage IVB Mucosal Melanoma of the Head and Neck", "Stage IVB Mucosal Melanoma of the Head and Neck AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Mucosal Melanoma of the Head and Neck AJCC v7", "shortest_name_length": 47}
{"curie": "MONDO:0013570", "names": ["COXPD8", "Combined Oxidative Phosphorylation Deficiency 8", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 8", "combined oxidative phosphorylation deficiency 8", "Combined Oxidative Phosphorylation Defect Type 8", "Combined oxidative phosphorylation defect type 8", "combined oxidative phosphorylation defect type 8", "AARS2 combined oxidative phosphorylation deficiency", "combined oxidative phosphorylation deficiency type 8", "COXPD8 - combined oxidative phosphorylation defect type 8", "cardiomyopathy, hypertrophic mitochondrial, fatal infantile", "Combined oxidative phosphorylation defect type 8 (disorder)", "CARDIOMYOPATHY, HYPERTROPHIC MITOCHONDRIAL, FATAL INFANTILE", "combined oxidative phosphorylation defect type 8 (diagnosis)", "combined oxidative phosphorylation deficiency caused by mutation in AARS2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation defect type 8", "shortest_name_length": 6}
{"curie": "UMLS:C0235074", "names": ["glossoplegia", "Glossoplegia", "TONGUE PARALYSIS", "Tongue paralysis", "paralysis; tongue", "tongue; paralysis", "Glossoplegia, NOS", "Paralysis of tongue", "Paralysis of tongue, NOS", "Paralysis of tongue (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paralysis of tongue", "shortest_name_length": 12}
{"curie": "UMLS:C0920103", "names": ["Hematotoxicity", "Haematotoxicity", "Hematotoxicosis", "Haematotoxicosis", "Haematotoxicity NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Haematotoxicity", "shortest_name_length": 14}
{"curie": "UMLS:C0280116", "names": ["stage III adult NHL", "NHL, stage III adult", "Stage III Non-Hodgkin Lymphoma", "Stage III Adult Non-Hodgkin Lymphoma", "stage III adult non-Hodgkin lymphoma", "Adult Non-Hodgkin's Lymphoma Stage III", "Stage III Adult Non-Hodgkin's Lymphoma", "non-Hodgkin's lymphoma, stage III adult", "adult non-Hodgkin's lymphoma, stage III", "lymphoma, stage III, adult non-Hodgkin's", "Ann Arbor Stage III Adult Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Adult Non-Hodgkin Lymphoma", "shortest_name_length": 19}
{"curie": "MONDO:0018006", "names": ["adult-onset distal myopathy due to VCP mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult-onset distal myopathy due to VCP mutation", "shortest_name_length": 47}
{"curie": "UMLS:C4520922", "names": ["stage I laryngeal cancer", "Stage I Larynx Carcinoma", "Stage I Laryngeal Cancer", "Laryngeal Cancer, Stage I", "Stage I Carcinoma of Larynx", "Stage I Laryngeal Carcinoma", "Stage I Laryngeal Throat Cancer", "Stage I Carcinoma of the Larynx", "Stage I Laryngeal Cancer AJCC v6", "Stage I Laryngeal Cancer AJCC v7", "Stage I Laryngeal Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Laryngeal Cancer AJCC v6 and v7", "shortest_name_length": 24}
{"curie": "UMLS:C4725797", "names": ["Recurrent Renal Pelvis Urothelial Cancer", "Recurrent Renal Pelvis Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Renal Pelvis Urothelial Carcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0006921", "names": ["actinomycosis", "Actinomycete Infection", "actinomycete infection", "actinomycete infections", "infection, actinomycete", "actinomycotic infection", "Infection, Actinomycete", "Actinomycete Infections", "Infections, Actinomycete", "infections, actinomycete", "Actinomycetales Infection", "Actinomycetales infection", "actinomycetales infection", "Actinomycetales Infections", "actinomycetales infections", "Infection, Actinomycetales", "infection, actinomycetales", "Infections, Actinomycetales", "infections, actinomycetales", "actinomycotic infectious disease", "Actinomycetales infectious disease", "actinomycetales disease or disorder", "infection caused by actinomycetales", "Infection caused by Actinomycetales", "actinomycetales caused disease or disorder", "primary Actinomycetales infectious disease", "Infection caused by Actinomycetales (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Actinomycetales infectious disease", "shortest_name_length": 13}
{"curie": "MONDO:0013610", "names": ["RP61", "RETINITIS PIGMENTOSA 61", "retinitis pigmentosa 61", "CLRN1 retinitis pigmentosa", "retinitis pigmentosa type 61", "retinitis pigmentosa caused by mutation in CLRN1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 61", "shortest_name_length": 4}
{"curie": "MONDO:0005328", "names": ["Oculopathy", "oculopathy", "Eye Disease", "Eye disease", "EYE ANOMALY", "eye disease", "Disease;eye", "EYE DISORDER", "eye diseases", "anomaly; eye", "eye; anomaly", "Abnormal eye", "Eye Disorder", "Eye disorder", "eye disorder", "Eye Diseases", "DISORDER EYE", "Disorder eye", "Eye disorders", "eye disorders", "eye; disorder", "anomalies eye", "Eye--Diseases", "Eye Disorders", "globe disease", "ophthalmopathy", "globe disorder", "GLOBE DISORDER", "deformity; eye", "disease of eye", "Ophthalmopathy", "eye; deformity", "Disorder of eye", "Occular disease", "Eye Abnormality", "disorder of eye", "eye abnormality", "EYE ABNORMALITY", "Eye abnormality", "Abnormality, Eye", "Eye disorder NOS", "Eye malformation", "EYE MALFORMATION", "disorder of globe", "Disorder of globe", "Eye Abnormalities", "Eye abnormalities", "abnormalities eye", "eye malformations", "eye abnormalities", "deformity; eyeball", "eyeball; deformity", "EYE DISORDER (NOS)", "Abnormalities, Eye", "disorders of globe", "Ophthalmopathy NOS", "Disorders of globe", "Disease of eyeball", "Eye--Abnormalities", "disease of eyeball", "Disorder of eyeball", "DISEASES OF THE EYE", "disorder of eyeball", "diseases of the eye", "Eye abnormality NOS", "Disease of eye, NOS", "OPHTHALMIC DISORDERS", "ophthalmic disorders", "EYE ABNORMALITY (NOS)", "Congenital eye disease", "EYE ANOMALY CONGENITAL", "Disorder of eye proper", "Congenital anomaly;eye", "Disorder of eye region", "disorder of eye proper", "Disorders of the globe", "Disorder of globe, NOS", "Abnormality of the eye", "congenital eye disorder", "congenital eye syndrome", "Congenital eye syndrome", "Congenital Eye Disorder", "congenital diseases eye", "Eye disease or syndrome", "congenital disorder eye", "Congenital eye disorder", "Eye disorders congenital", "Congenital eye anomalies", "Congenital anomaly of eye", "Ophthalmological disorder", "OPHTHAMOLOGIC ABNORMALITY", "eye disorders (diagnosis)", "Ophthalmologic Abnormality", "Disorder of orbital region", "Congenital ocular syndrome", "Unspecified anomaly of eye", "congenital eye abnormality", "Congenital deformity of eye", "congenital anomalies of eye", "Congenital anomalies of eye", "Unspecified disorder of eye", "Ophthalmologic abnormalities", "Congenital eye malformations", "Disorder of eye, unspecified", "Congenital eye deformity NOS", "Eye deformity congenital NOS", "Congenital anomaly NOS of eye", "Congenital abnormality of eye", "congenital anomaly of the eye", "Unspecified disorder of globe", "Diseases and Syndromes of Eye", "DISORDERS AFFECTING THE GLOBE", "disorders of globe (diagnosis)", "Congenital anomaly of eye, NOS", "Congenital malformation of eye", "disease (or disorder); eyeball", "Disorder of globe, unspecified", "Congenital syndrome of the eye", "OPHTHALMOLOGIC ABNORMALITY, NOS", "Congenital deformity NOS of eye", "Congenital anomaly of the globe", "Congenital deformity of eye, NOS", "Disorder of eye region (disorder)", "Disorder of eye proper (disorder)", "General Eye Diseases and Syndromes", "eyeball of camera-type eye disease", "Congenital anomaly of eye (disorder)", "Congenital Ophthalmologic Abnormality", "disease of eyeball of camera-type eye", "Other degenerative disorders of globe", "Congenital disease or syndrome of eye", "Unspecified anomaly of eye, congenital", "disorder of eyeball of camera-type eye", "congenital anomalies of eye (diagnosis)", "Congenital Diseases and Syndromes of Eye", "CONGENITAL ANOMALIES OF THE EYE AND ORBIT", "Congenital anomaly NOS of any part of eye", "Congenital deformity NOS of any part of eye", "Congenital malformation of eye, unspecified", "eyeball of camera-type eye disease or disorder", "disease or disorder of eyeball of camera-type eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eye disorder", "shortest_name_length": 10}
{"curie": "UMLS:C4763738", "names": ["Complication due to Medical/Surgical Care"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Complication due to Medical/Surgical Care", "shortest_name_length": 41}
{"curie": "MONDO:0010788", "names": ["LHON", "Leber Disease", "atrophy; Leber", "Lebers Disease", "Leber; atrophy", "Leber's disease", "Leber's Disease", "Leber’s disease", "Disease, Leber's", "Leber's Diseases", "Diseases, Leber's", "Leber optic atrophy", "LEBER OPTIC ATROPHY", "Leber Optic Atrophy", "leber optic atrophy", "Optic Atrophy, Leber", "Leber; optic atrophy", "optic atrophy; Leber", "Leber's Optic Atrophy", "leber's optic atrophy", "Leber's optic atrophy", "Leber Optic Neuropathy", "Optic atrophy, Leber's", "Atrophy, optic, Leber's", "Lebers Optic Neuropathy", "Leber's Optic Neuropathy", "Leber optic degeneration", "optic atrophy, Leber type", "Optic Atrophy, Leber Type", "Optic Neuropathy, Leber's", "Neuropathy, Leber's Optic", "Leber optic atrophy features", "Leber Hereditary optic atrophy", "Leber Hereditary Optic Atrophy", "Leber's Hereditary Optic Atrophy", "Leber Optic Atrophy and Dystonia", "Leber's optic atrophy (disorder)", "Optic Atrophy, Leber, Hereditary", "Optic Atrophy, Hereditary, Leber", "Leber's optic atrophy (diagnosis)", "Hereditary Optic Neuroretinopathy", "LEBER HEREDITARY OPTIC NEUROPATHY", "Leber Hereditary Optic Neuropathy", "Leber hereditary optic neuropathy", "Neuroretinopathy, Hereditary Optic", "Optic Neuroretinopathy, Hereditary", "Hereditary Optic Neuroretinopathies", "Leber's hereditary optic neuropathy", "Leber's Hereditary Optic Neuropathy", "Optic Neuroretinopathies, Hereditary", "Neuroretinopathies, Hereditary Optic", "LHON - Leber hereditary optic neuropathy", "LHON (Leber's hereditary optic neuropathy)", "LHON - Leber's hereditary optic neuropathy", "Leber's hereditary optic neuropathy (LHON)", "Leber's hereditary optic atrophy neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leber hereditary optic neuropathy", "shortest_name_length": 4}
{"curie": "UMLS:C5206597", "names": ["Paratesticular Leiomyoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paratesticular Leiomyoma", "shortest_name_length": 24}
{"curie": "UMLS:C0275521", "names": ["Clinical infection", "Clinical Infection", "clinical infection", "infection clinical", "clinical infections", "Clinical infection (disorder)", "infectious disease - clinical", "Clinical infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical infection", "shortest_name_length": 18}
{"curie": "MONDO:0008735", "names": ["Adrenocortical Unresponsiveness To Acth With Postreceptor Defect", "adrenocortical unresponsiveness to ACTH with postreceptor defect", "ADRENOCORTICAL UNRESPONSIVENESS TO ACTH WITH POSTRECEPTOR DEFECT", "FAMILIAL GLUCOCORTICOID DEFICIENCY DUE TO DEFECT DISTAL TO ACTH RECEPTOR", "familial glucocorticoid deficiency due to defect distal to ACTH receptor", "Familial Glucocorticoid Deficiency Due To Defect Distal To Acth Receptor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adrenocortical unresponsiveness to ACTH with postreceptor defect", "shortest_name_length": 64}
{"curie": "MONDO:0022953", "names": ["delta-1-pyrroline-5-carboxylate dehydrogenase deficiency", "1-pyrroline-5-carboxylate dehydrogenase activity disease", "disorder of 1-pyrroline-5-carboxylate dehydrogenase activity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "delta-1-pyrroline-5-carboxylate dehydrogenase deficiency", "shortest_name_length": 56}
{"curie": "UMLS:C5206449", "names": ["Stage IIIA Cervical Cancer FIGO 2018", "Stage IIIA Cervical Carcinoma FIGO 2018"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Cervical Cancer FIGO 2018", "shortest_name_length": 36}
{"curie": "MONDO:0015304", "names": ["arachnitis", "Arachnitis", "ARACHNOIDITIS", "Arachnoiditis", "arachnoiditis", "Arachnoiditides", "arachnoiditis NOS", "Arachnoiditis, NOS", "Adhesive arachnitis", "chronic arachnoiditis", "Chronic arachnoiditis", "Adhesive arachnoiditis", "arachnoiditis adhesive", "adhesive arachnoiditis", "Arachnoiditis (disorder)", "arachnoiditis (diagnosis)", "arachnoid mater inflammation", "Arachnoid Membrane Inflammation", "inflammation of arachnoid mater", "Inflammation, Arachnoid Membrane", "Arachnoid Membrane Inflammations", "Inflammations, Arachnoid Membrane", "Adhesive arachnoiditis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arachnoiditis", "shortest_name_length": 10}
{"curie": "UMLS:C4743579", "names": ["Unresectable Pleural Malignant Mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Pleural Malignant Mesothelioma", "shortest_name_length": 43}
{"curie": "UMLS:C0023220", "names": ["injury leg", "Injury;leg", "LEG INJURY", "leg injury", "Leg Injury", "Leg injury", "Injury, Leg", "Leg Injuries", "leg injuries", "injuries leg", "Injuries, Leg", "injury to leg", "lower limb injury", "injuries limb lower", "injury; limb, lower", "Injury of lower limb", "disorders injuries leg", "LOWER EXTREMITY INJURY", "extremity injuries lower", "Injury of lower extremity", "Injury to lower extremity", "injury of lower extremity", "Injury of lower limb (disorder)", "injury of lower extremity (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leg Injuries", "shortest_name_length": 10}
{"curie": "MONDO:0032917", "names": ["DFNA76", "deafness, autosomal dominant 76", "DEAFNESS, AUTOSOMAL DOMINANT 76", "hearing loss, autosomal dominant 76", "autosomal dominant nonsyndromic deafness 76"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal dominant 76", "shortest_name_length": 6}
{"curie": "UMLS:C0012765", "names": ["disorder; salivary secretion", "salivary secretion; disorder", "Salivary secretion disturbance", "salivary secretion disturbance", "disturbance; salivary secretion", "Disturbance of salivary secretion", "disturbance of salivary secretion", "Disturbances of salivary secretion", "deficiency; secretion salivary gland", "deficiency; salivary gland secretion", "Disturbance of salivary secretion, NOS", "salivary gland; deficiency (secretion)", "Disturbance of salivary secretion (disorder)", "disturbance of salivary secretion (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disturbance of salivary secretion", "shortest_name_length": 28}
{"curie": "MONDO:0016127", "names": ["Purulent myositis", "Myositis, purulent", "myositis; purulent", "Bacterial myositis", "purulent; myositis", "bacterial myositis", "Suppurative myositis", "myositis; suppurative", "suppurative; myositis", "Myositis, suppurative", "Purulent myositis (disorder)", "bacterial myositis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bacterial myositis", "shortest_name_length": 17}
{"curie": "UMLS:C5419579", "names": ["Mold or Dust Allergy", "Allergy, Mold or Dust"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mold or Dust Allergy", "shortest_name_length": 20}
{"curie": "MONDO:0009571", "names": ["MKS", "Mes", "MES", "MKS1", "Meckel Syndrome", "MECKEL SYNDROME", "GRUBER SYNDROME", "Meckel syndrome", "Gruber syndrome", "Meckel syndrome 1", "MKS1 Meckel syndrome", "Meckel syndrome type1", "Meckel Gruber syndrome", "Meckel-Gruber syndrome", "Meckel-Gruber Syndrome", "MECKEL-GRUBER SYNDROME", "Meckel syndrome type 1", "MECKEL SYNDROME, TYPE 1", "Meckel syndrome, type 1", "Meckel Syndrome, Type 1", "Dysencephalia splachnocystica", "MECKEL-GRUBER SYNDROME, TYPE 1", "Meckel-Gruber syndrome, type 1", "Meckel-Gruber Syndrome, Type 1", "Dysencephalia Splanchnocystica", "DYSENCEPHALIA SPLANCHNOCYSTICA", "Meckel syndrome type 1 (diagnosis)", "Meckel syndrome caused by mutation in MKS1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meckel syndrome, type 1", "shortest_name_length": 3}
{"curie": "MONDO:0010735", "names": ["KD", "XBSN", "SBMA", "SMAX1", "X-linked BSMA", "Kennedy disease", "Kennedy Disease", "KENNEDY DISEASE", "Kennedy syndrome", "Kennedy Syndrome", "Kennedy's Disease", "Kennedy's disease", "kennedy's syndrome", "Kennedy's syndrome", "Kennedy disease (diagnosis)", "spinobulbar muscular atrophy", "X-linked bulbospinal atrophy", "Spinobulbar Muscular Atrophy", "Bulbospinal muscular atrophy", "Muscular Atrophy, Spinobulbar", "Atrophy, Spinobulbar Muscular", "X-Linked Bulbo-Spinal Atrophy", "X Linked Bulbo Spinal Atrophy", "X-linked bulbo-spinal atrophy", "Bulbo Spinal Atrophy, X Linked", "Atrophy, X-Linked Bulbo-Spinal", "Bulbo-Spinal Atrophy, X-Linked", "spinal bulbar muscular atrophy", "Atrophy, Muscular, Spinobulbar", "Spinobulbar Muscular Atrophies", "X-linked bulbospinal amyotrophy", "X-Linked Bulbo-Spinal Atrophies", "Atrophies, X-Linked Bulbo-Spinal", "Bulbo-Spinal Atrophies, X-Linked", "spinal and bulbar muscular atrophy", "SPINAL AND BULBAR MUSCULAR ATROPHY", "Spinal and Bulbar Muscular Atrophy", "X-linked bulbospinal muscular atrophy", "X-linked Bulbospinal Muscular Atrophy", "X linked Bulbospinal Muscular Atrophy", "Bulbospinal Muscular Atrophy, X linked", "Bulbospinal Muscular Atrophy, X-linked", "BULBOSPINAL MUSCULAR ATROPHY, X-LINKED", "bulbospinal muscular atrophy, X-linked", "KENNEDY SPINAL AND BULBAR MUSCULAR ATROPHY", "Kennedy Spinal and Bulbar Muscular Atrophy", "Kennedy spinal and bulbar muscular atrophy", "X-linked Spinal and Bulbar Muscular Atrophy", "X-Linked Spinal and Bulbar Muscular Atrophy", "X Linked Spinal and Bulbar Muscular Atrophy", "X-linked spinal and bulbar muscular atrophy", "Bulbospinal neuronopathy, X-linked recessive", "bulbospinal neuronopathy, X-linked recessive", "BULBOSPINAL NEURONOPATHY, X-LINKED RECESSIVE", "Spinal And Bulbar Muscular Atrophy, X Linked 1", "spinal and bulbar muscular atrophy, X-linked 1", "Spinal And Bulbar Muscular Atrophy, X-Linked 1", "SPINAL AND BULBAR MUSCULAR ATROPHY, X-LINKED 1", "Spinal and Bulbar Muscular Atrophy, X-linked 1", "spinal and bulbar muscular atrophy, X-linked type 1", "spinal and bulbar muscular atrophy of Kennedy, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kennedy disease", "shortest_name_length": 2}
{"curie": "UMLS:C1333562", "names": ["FIGO Stage IVC GTT", "FIGO Stage IVC Gestational Trophoblastic Tumor", "FIGO Stage IVC Gestational Trophoblastic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Stage IVC Gestational Trophoblastic Tumor", "shortest_name_length": 18}
{"curie": "UMLS:C1335896", "names": ["Canalicular adenoma", "Salivary Gland Canalicular Adenoma", "canalicular adenoma of salivary gland", "Canalicular Adenoma of Salivary Gland", "Canalicular Adenoma of the Salivary Gland", "canalicular adenoma of salivary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canalicular adenoma of salivary gland", "shortest_name_length": 19}
{"curie": "MONDO:0007775", "names": ["Familial hypersecretion of adrenal androgens", "familial hypersecretion of adrenal androgens", "Hypersecretion of adrenal androgens, familial", "HYPERSECRETION OF ADRENAL ANDROGENS, FAMILIAL", "hypersecretion of adrenal androgens, familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypersecretion of adrenal androgens, familial", "shortest_name_length": 44}
{"curie": "MONDO:0010336", "names": ["OFD8", "Ofds 8", "OFDS VIII", "OFD syndrome 8", "Edwards syndrome", "orofaciodigital syndrome 8", "Orofaciodigital syndrome 8", "OROFACIODIGITAL SYNDROME VIII", "orofaciodigital syndrome VIII", "Orofaciodigital syndrome VIII", "oral facial digital syndrome 8", "Oral-facial-digital syndrome 8", "digito-orofacial syndrome VIII", "Orofaciodigital syndrome type 8", "orofaciodigital syndrome type 8", "oral-facial-digital syndrome VIII", "orofaciodigital syndrome type VIII", "Oro-facial digital syndrome type 8", "Oral-facial-digital syndrome type 8", "oral facial digital syndrome type 8", "orofaciodigital (OFD) syndrome VIII", "oral-facial-digital syndrome type 8", "oral-Facial-digital syndrome, type 8", "Orofaciodigital syndrome Edwards type", "Orofaciodigital syndrome, Edwards type", "orofaciodigital syndrome, Edwards type", "ORAL-FACIAL-DIGITAL SYNDROME, TYPE VIII", "Oral-facial-digital syndrome Edwards type", "Oral-facial-digital syndrome, Edwards type", "oral-facial-digital syndrome, Edwards type", "Oro-facial digital syndrome type 8 (disorder)", "oral-facial-digital syndrome type 8 (diagnosis)", "orofaciodigital syndrome VIII, X-linked recessive", "oral-Facial-digital syndrome with hypoplastic Epiglottis", "ORAL-FACIAL-DIGITAL SYNDROME WITH HYPOPLASTIC EPIGLOTTIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orofaciodigital syndrome VIII", "shortest_name_length": 4}
{"curie": "UMLS:C5552983", "names": ["SMILE", "Stratified Mucin-Producing Intraepithelial Lesion", "Cervical Stratified Mucin-Producing Intraepithelial Lesion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Stratified Mucin-Producing Intraepithelial Lesion", "shortest_name_length": 5}
{"curie": "MONDO:0011030", "names": ["EBCR", "Ebcr", "epithelial basolateral chloride conductance regulator, rabbit, homolog of", "EPITHELIAL BASOLATERAL CHLORIDE CONDUCTANCE REGULATOR, RABBIT, HOMOLOG OF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epithelial basolateral chloride conductance regulator, rabbit, homolog of", "shortest_name_length": 4}
{"curie": "MONDO:0013653", "names": ["PARK18", "Parkinson disease 18", "PARKINSON DISEASE 18", "EIF4G1 hereditary late onset Parkinson disease", "susceptibility to autosomal dominant Parkinson disease 18", "PARKINSON DISEASE 18, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO", "Parkinson disease 18, autosomal dominant, susceptibility to", "hereditary late onset Parkinson disease caused by mutation in EIF4G1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parkinson disease 18, autosomal dominant, susceptibility to", "shortest_name_length": 6}
{"curie": "UMLS:C4528563", "names": ["Perineal Ectopic Fibroadenoma", "Fibroadenoma of Anogenital Mammary-Like Glands", "Fibroadenoma of Anogenital Mammary-Type Glands"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fibroadenoma of Anogenital Mammary-Type Glands", "shortest_name_length": 29}
{"curie": "MONDO:0011340", "names": ["stenosis of trachea", "Congenital narrowed trachea", "congenital tracheal stenosis", "Stenosis;tracheal;congenital", "Congenital stenosis, trachea", "Congenital tracheal stenosis", "trachea; stenosis, congenital", "Tracheal stenosis, congenital", "stenosis; trachea, congenital", "stricture; trachea, congenital", "Congenital stenosis of trachea", "trachea; stricture, congenital", "stenosis of trachea (diagnosis)", "Congenital tracheobronchial stenosis", "tracheobronchial stenosis, congenital", "TRACHEOBRONCHIAL STENOSIS, CONGENITAL", "Tracheobronchial Stenosis, Congenital", "Congenital stenosis of trachea (disorder)", "Congenital stenosis of the tracheobronchial tree", "Congenital stenosis of the tracheobronchial tree (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital tracheal stenosis", "shortest_name_length": 19}
{"curie": "MONDO:0004810", "names": ["Acute ethmoiditis", "acute ethmoiditis", "acute ethmoid sinusitis", "ethmoidal sinus - acute", "ethmoid sinusitis, acute", "Acute ethmoidal sinusitis", "acute ethmoidal sinusitis", "Acute sinusitis, ethmoidal", "sinusitis; acute, ethmoidal", "sinusitis; ethmoidal, acute", "Acute ethmoidal sinusitis (disorder)", "acute ethmoidal sinusitis (diagnosis)", "Acute ethmoidal sinusitis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute ethmoiditis", "shortest_name_length": 17}
{"curie": "MONDO:0054860", "names": ["DFNB110", "autosomal recessive deafness 110", "deafness, autosomal recessive 110", "DEAFNESS, AUTOSOMAL RECESSIVE 110", "hearing loss, autosomal recessive 110", "autosomal recessive nonsyndromic deafness 110"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal recessive 110", "shortest_name_length": 7}
{"curie": "MONDO:0006158", "names": ["colorectal DLBCL", "Colorectal DLBCL", "Colorectal Diffuse Large B-Cell Lymphoma", "colorectum diffuse large B-cell lymphoma", "colorectal diffuse large B-cell lymphoma", "diffuse large B-cell lymphoma of colorectum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorectal diffuse large B-cell lymphoma", "shortest_name_length": 16}
{"curie": "MONDO:0008685", "names": ["WPW", "wpw", "wpws", "Kent Bundle", "syndrome wpw", "WPW syndrome", "WPW SYNDROME", "wpw syndrome", "WPW Syndrome", "Wpw syndrome", "Bundle, Kent", "Syndrome, WPW", "Bundle of Kent", "PRE-EXCITATION", "Pre-excitation", "accessory pathway", "Accessory pathway", "accessory pathways", "Preexcitation Syndrome", "Preexcitation syndrome", "preexcitation syndrome", "PREEXCITATION SYNDROME", "pre-excitation syndrome", "Pre-Excitation Syndrome", "Preexcitation Syndromes", "Pre-excitation syndrome", "Pre Excitation Syndromes", "Pre-Excitation Syndromes", "anomalous A-V excitation", "Anomalous A-V excitation", "Ventricular preexcitation", "Accessory Conducting Pathway", "parkinson wolf white syndrome", "Wolf-Parkinson-White syndrome", "wolf white parkinson syndrome", "Accessory Conducting Pathways", "Wolff-Parkinson-White pattern", "Conducting Pathway, Accessory", "wolf-parkinson-white syndrome", "Wolf Parkinson White Syndrome", "Pathway, Accessory Conducting", "wolf parkinson white syndrome", "Wolf-Parkinson-White Syndrome", "parkinsons syndrome white wolf", "wolff parkinson white syndrome", "wolff-Parkinson-White syndrome", "Conducting Pathways, Accessory", "parkinson syndrome whites wolf", "Syndrome, Wolf-Parkinson-White", "WOLFF PARKINSON WHITE SYNDROME", "wolff-parkinson-white syndrome", "Wolff-Parkinson-White Syndrome", "parkinson syndrome white wolff", "Wolff Parkinson White Syndrome", "WOLFF-PARKINSON-WHITE SYNDROME", "syndrome wolf parkinsons white", "Wolff-Parkinson-White syndrome", "Wolff Parkinson White syndrome", "syndrome wolff-parkinson-white", "wolff parkinson syndrome white", "Pathways, Accessory Conducting", "parkinsons syndrome white wolfs", "parkinson syndrome whites wolfs", "Syndrome, Wolff-Parkinson-White", "syndrome wolff parkinsons white", "parkinsons syndrome white wolff", "Wolff-Parkinson-White arrhythmia", "Accessory Atrioventricular Bundle", "False Bundle-Branch Block Syndrome", "Accessory Atrioventricular Pathway", "Atrioventricular accessory pathway", "Bundle, Accessory Atrioventricular", "Accessory Atrioventricular Bundles", "Atrioventricular Bundle, Accessory", "ACCESSORY ATRIOVENTRICULAR PATHWAYS", "pre-excitation syndrome (diagnosis)", "Atrioventricular Pathway, Accessory", "accessory atrioventricular pathways", "Bundles, Accessory Atrioventricular", "Atrioventricular Bundles, Accessory", "Accessory Atrioventricular Pathways", "Pathway, Accessory Atrioventricular", "WPW - Wolff-Parkinson-White pattern", "WPW - Wolff-Parkinson-White syndrome", "Pathways, Accessory Atrioventricular", "atrioventricular; excitation anomaly", "Atrioventricular Pathways, Accessory", "anomaly; atrioventricular excitation", "Wolff-Parkinson-White (WPW) syndrome", "Accessory atrioventricular conduction", "Anomalous atrioventricular excitation", "anomalous atrioventricular excitation", "accessory; atrioventricular conduction", "atrioventricular; conduction accessory", "ATRIOVENTRICULAR EXCITATION, ANOMALOUS", "Atrioventricular conduction, accessory", "accelerated atrioventricular conduction", "Wolff-Parkinson-White pattern (finding)", "Accelerated atrioventricular conduction", "Wolff-Parkinson-white syndrome (disease)", "Atrioventricular conduction, accelerated", "Wolff-Parkinson-White pattern (disorder)", "WOLFF PARKINSON WHITE SYNDROME CONGENITAL", "Anomalous Ventricular Excitation Syndrome", "Wolff-Parkinson-White syndrome congenital", "Pre-excitation atrioventricular conduction", "Wolff Parkinson White syndrome (diagnosis)", "Ventricular Pre-Excitation with Arrhythmia", "pre-excitation atrioventricular conduction", "Ventricular pre-excitation with arrhythmia", "Atrioventricular conduction, pre-excitation", "ventricular familial preexcitation syndrome", "Accessory Atrioventricular Bundle (disorder)", "Auriculoventricular Accessory Pathway Syndrome", "Ventricular pre-excitation with arrhythmia, NOS", "Wolff-Parkinson-White ventricular preexcitation", "Anomalous atrioventricular excitation (disorder)", "Ventricular preexcitation, Wolff-Parkinson-White", "anomalous atrioventricular excitation (diagnosis)", "Accelerated atrioventricular conduction (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wolff-Parkinson-White syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C2981625", "names": ["Stage II Intrahepatic Cholangiocarcinoma", "Stage II Intrahepatic Cholangiocarcinoma AJCC v7", "Stage II Intrahepatic Bile Duct Cancer (Cholangiocarcinoma)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Intrahepatic Cholangiocarcinoma AJCC v7", "shortest_name_length": 40}
{"curie": "MONDO:0020247", "names": ["Vitreoretinal dysplasia", "vitreoretinal dysplasia", "congenital vitreoretinal dysplasia", "Vitreoretinal dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital vitreoretinal dysplasia", "shortest_name_length": 23}
{"curie": "MONDO:0100005", "names": ["primary MACS", "primary mast cell activation syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary mast cell activation syndrome", "shortest_name_length": 12}
{"curie": "UMLS:C3827806", "names": ["Tortuous colon", "Tortuous Colon", "tortuous colon", "Tortuous colon (disorder)", "tortuous colon (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tortuous colon", "shortest_name_length": 14}
{"curie": "UMLS:C0475072", "names": ["Traumatic Cerebral Hemorrhage", "traumatic cerebral hemorrhage", "Traumatic cerebral hemorrhage", "Cerebral hemorrhage traumatic", "traumatic cerebral haemorrhage", "Traumatic Cerebral Hemorrhages", "Hemorrhage, Traumatic Cerebral", "Traumatic cerebral haemorrhage", "Cerebral Hemorrhage, Traumatic", "Cerebral haemorrhage traumatic", "Haemorrhage;cerebral;traumatic", "Hemorrhages, Traumatic Cerebral", "Cerebral Hemorrhages, Traumatic", "Traumatic intracerebral hemorrhage", "Traumatic cerebral hemorrhage, NOS", "Traumatic Intracerebral Hemorrhage", "Hemorrhage, Traumatic Intracerebral", "Traumatic intracerebral haemorrhage", "Traumatic Intracerebral Hemorrhages", "Traumatic cerebral haemorrhage, NOS", "Intracerebral Hemorrhage, Traumatic", "Intracerebral Hemorrhages, Traumatic", "Cerebral hemorrhage following injury", "Hemorrhages, Traumatic Intracerebral", "Cerebral haemorrhage following injury", "Brain Hemorrhage, Cerebral, Traumatic", "traumatic cerebral hemorrhage (diagnosis)", "Traumatic Cerebral Parenchymal Hemorrhage", "Cerebral Parenchymal Hemorrhage, Traumatic", "Traumatic Cerebral Intraparenchymal Hemorrhage", "Cerebral Intraparenchymal Hemorrhage, Traumatic", "Cerebral hemorrhage following injury (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Traumatic cerebral hemorrhage", "shortest_name_length": 29}
{"curie": "MONDO:0004539", "names": ["aorta cancer", "cancer of aorta", "Aortic Malignant Tumor", "aortic malignant tumor", "malignant tumor of aorta", "Malignant Tumor of Aorta", "malignant aorta neoplasm", "aortic malignant neoplasm", "Malignant Aortic Neoplasm", "Aortic Malignant Neoplasm", "malignant aortic neoplasm", "Malignant Neoplasm of Aorta", "malignant neoplasm of aorta", "Malignant Tumor of the Aorta", "malignant tumor of the aorta", "malignant neoplasm of the aorta", "Malignant Neoplasm of the Aorta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic malignant tumor", "shortest_name_length": 12}
{"curie": "MONDO:0022316", "names": ["Calderon Gonzalez-Cantu syndrome", "Calderón González Cantu syndrome", "Calderón-González-Cantu syndrome", "hair defect with photosensitivity and mental retardation", "Hair defect with photosensitivity and mental retardation", "HAIR DEFECT WITH PHOTOSENSITIVITY AND MENTAL RETARDATION", "hair defect with photosensitivity and intellectual disability", "hair defect-photosensitivity-intellectual disability syndrome", "Hair defect with photosensitivity and intellectual disability syndrome", "hair defect with photosensitivity and intellectual disability syndrome", "Hair defect with photosensitivity and intellectual disability syndrome (disorder)", "hair defect with photosensitivity and intellectual disability syndrome (diagnosis)", "kinky hair, photosensitivity, broken eyebrows and eyelashes, and nonprogressive mental retardation", "Kinky hair, photosensitivity, broken eyebrows and eyelashes, and nonprogressive mental retardation", "kinky hair, photosensitivity, broken eyebrows and eyelashes, and nonprogressive intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hair defect with photosensitivity and intellectual disability syndrome", "shortest_name_length": 32}
{"curie": "MONDO:0008181", "names": ["absence of palmaris longus muscle", "PALMARIS LONGUS MUSCLE, ABSENCE OF", "palmaris longus muscle, absence of", "absence of palmaris longus muscle (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "palmaris longus muscle, absence of", "shortest_name_length": 33}
{"curie": "MONDO:0021449", "names": ["benign gastric tumor", "stomach benign tumor", "benign stomach tumor", "Gastric benign tumor", "Benign Gastric Tumor", "benign gastric tumors", "Benign Stomach Tumors", "benign stomach tumors", "Benign Gastric Tumors", "stomach tumors, benign", "Gastric Tumors, Benign", "gastric tumors, benign", "Stomach Tumors, Benign", "benign gastric neoplasm", "stomach benign neoplasm", "Benign Gastric Neoplasm", "Benign gastric neoplasm", "Benign tumor of stomach", "benign tumor of stomach", "Benign Tumor of Stomach", "Benign tumour of stomach", "Benign Tumors of Stomach", "benign stomach neoplasms", "Benign Stomach Neoplasms", "benign tumors of stomach", "Gastric Neoplasms, Benign", "gastric neoplasms, benign", "Stomach Neoplasms, Benign", "stomach neoplasms, benign", "benign neoplasm of stomach", "Benign Neoplasm of Stomach", "Benign neoplasm of stomach", "benign tumor of the stomach", "Benign Tumor of the Stomach", "Benign Tumors of the Stomach", "benign tumors of the stomach", "benign neoplasm of the stomach", "Benign Neoplasm of the Stomach", "Benign neoplasm of stomach, NOS", "Benign neoplasm of stomach (disorder)", "benign neoplasm of stomach (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of stomach", "shortest_name_length": 20}
{"curie": "MONDO:0006353", "names": ["Paranasal Sinus Papilloma", "paranasal sinus Schneiderian papilloma", "accessory sinus Schneiderian papilloma", "Paranasal Sinus Schneiderian Papilloma", "Accessory Sinus Schneiderian Papilloma", "Schneiderian Papilloma of Accessory Sinus", "Schneiderian papilloma of accessory sinus", "Schneiderian papilloma of paranasal sinus", "Schneiderian Papilloma of Paranasal Sinus", "Schneiderian papilloma of the accessory sinus", "Schneiderian Papilloma of the Paranasal Sinus", "Schneiderian Papilloma of the Accessory Sinus", "Schneiderian papilloma of the paranasal sinus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paranasal sinus Schneiderian papilloma", "shortest_name_length": 25}
{"curie": "MONDO:0002779", "names": ["CNS Chondroma", "CNS chondroma", "chondroma of CNS", "Chondroma of CNS", "CNS Osteochondroma", "CNS osteochondroma", "chondroma of the CNS", "Chondroma of the CNS", "Osteochondroma of CNS", "osteochondroma of CNS", "osteochondroma of the CNS", "Osteochondroma of the CNS", "central nervous system chondroma", "Central Nervous System Chondroma", "chondroma of central nervous system", "Chondroma of Central Nervous System", "Central Nervous System Osteochondroma", "central nervous system osteochondroma", "chondroma of the central nervous system", "Chondroma of the Central Nervous System", "osteochondroma of central nervous system", "Osteochondroma of Central Nervous System", "osteochondroma of the central nervous system", "Osteochondroma of the Central Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system chondroma", "shortest_name_length": 13}
{"curie": "MONDO:0056795", "names": ["SPGFX1", "Germinal cell aplasia", "Del Castillo syndrome", "Sertoli cell-only syndrome", "X-linked spermatogenic failure 1", "spermatogenic failure, X-linked, 1", "spermatogenic failure, X-linked, type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked spermatogenic failure 1", "shortest_name_length": 6}
{"curie": "MONDO:0004389", "names": ["acariasis", "Acariasis", "Acarinosis", "Acariasis NOS", "mite infestation", "Mite Infestation", "Mite infestation", "Mite Infestations", "Infestation, Mite", "mite infestations", "Acarine dermatitis", "Acarine dermatosis", "infestation; mites", "Infestations, Mite", "dermatitis; acarine", "Cutaneous acariasis", "Acariasis (disorder)", "infestation by mites", "acariasis (diagnosis)", "Mite infestation, NOS", "Infestation by Acarina", "Acariasis, unspecified", "Infestation (by);mites", "Dermatosis due to mites", "Infestation by mites NOS", "Dermatosis caused by mites", "Infestation by Acarina, NOS", "infestation by mites (diagnosis)", "Dermatosis caused by mites (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mite infestation", "shortest_name_length": 9}
{"curie": "MONDO:0018324", "names": ["late-onset myasthenia gravis", "adult-onset myasthenia gravis", "adult-onset acquired myasthenia", "adult-onset autoimmune myasthenia gravis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult-onset myasthenia gravis", "shortest_name_length": 28}
{"curie": "MONDO:0022890", "names": ["craniosynostosis Fontaine type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniosynostosis Fontaine type", "shortest_name_length": 30}
{"curie": "UMLS:C0920186", "names": ["Hepatic artery stenosis", "hepatic artery stenosis", "Stenosis of hepatic artery", "hepatic artery stenosis (diagnosis)", "Stenosis of hepatic artery (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatic artery stenosis", "shortest_name_length": 23}
{"curie": "UMLS:C0238311", "names": ["Nicotinism", "nicotine poison", "NICOTINE POISONING", "nicotine poisoning", "Nicotine poisoning", "Nicotine poisoning (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nicotine poisoning", "shortest_name_length": 10}
{"curie": "MONDO:0003482", "names": ["body lice", "Body Lice", "lice body", "Body lice", "Body louse", "body louse", "lice; body lice", "Body pediculosis", "Pediculus corporis", "PEDICULOSIS CORPORIS", "pediculosis corporis", "Pediculosis corporis", "body lice infestation", "body louse infestation", "Body louse infestation", "Body-louse infestation", "Infestation (by);lice;body", "body lice (physical finding)", "Pediculus humanus infestation", "Pediculus corporis infestation", "Pediculus corporis - body lice", "Pediculus corporis (body louse)", "Pediculus corporis [body louse]", "Pediculosis corporis (disorder)", "pediculosis corporis (diagnosis)", "Pediculus humanus corporis infection", "Pediculus humanus corporis infestation", "infections, Pediculus humanus corporis", "pediculosis; Pediculus humanus corporis", "Pediculus humanus corporis; pediculosis", "Pediculosis due to Pediculus humanus corporis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pediculus humanus corporis infestation", "shortest_name_length": 9}
{"curie": "MONDO:0016712", "names": ["Classic Medulloblastoma", "Classic medulloblastoma", "classic medulloblastoma", "Medulloblastoma, classic", "Classic medulloblastoma (disorder)", "classic medulloblastoma (diagnosis)", "Classic medulloblastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "classic medulloblastoma", "shortest_name_length": 23}
{"curie": "MONDO:0012792", "names": ["MTDPS8B", "MTDPS8A", "MNGIE, RRM2B-RELATED", "Mngie, Rrm2b-Related", "Mngie, Rrm2B-related", "mitochondrial DNA depletion syndrome 8b", "mitochondrial DNA depletion syndrome 8a", "RRM2B mitochondrial DNA depletion syndrome", "mitochondrial DNA depletion syndrome type 8a", "encephalomyopathic type with renal tubulopathy", "RRM2B-related mitochondrial DNA depletion syndrome", "MITOCHONDRIAL DNA DEPLETION SYNDROME 8B (MNGIE TYPE)", "mitochondrial DNA depletion syndrome 8B (Mngie type)", "mitochondrial DNA depletion syndrome caused by mutation in RRM2B", "mtDNA depletion syndrome, encephalomyopathic form with renal tubulopathy", "Mitochondrial Neurogastrointestinal Encephalopathy Syndrome, Rrm2b-Related", "MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOPATHY SYNDROME, RRM2B-RELATED", "mitochondrial neurogastrointestinal encephalopathy syndrome, RRM2B-related", "mitochondrial neurogastrointestinal encephalopathy syndrome, Rrm2B-related", "mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy", "Mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy", "Mitochondrial DNA depletion syndrome 8A encephalomyopathic type with renal tubulopathy", "MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY)", "mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy)", "RRM2B-related mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy", "mitochondrial DNA depletion syndrome, encephalomyopathic, with renal tubulopathy, autosomal recessive", "MITOCHONDRIAL DNA DEPLETION SYNDROME, ENCEPHALOMYOPATHIC, WITH RENAL TUBULOPATHY, AUTOSOMAL RECESSIVE", "Ribonucleotide reductase regulatory TP53 inducible subunit M2B-related mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form with renal tubulopathy", "Ribonucleotide reductase regulatory TP53 inducible subunit M2B-related mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form with renal tubulopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial DNA depletion syndrome 8a", "shortest_name_length": 7}
{"curie": "MONDO:0013423", "names": ["LCAPD2", "MASP2 deficiency", "MASP2 Deficiency", "MASP2 DEFICIENCY", "immunodeficiency due to MASP-2 deficiency", "LECTIN COMPLEMENT ACTIVATION PATHWAY, DEFECT IN, 2", "lectin complement activation pathway, defect in, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency due to MASP-2 deficiency", "shortest_name_length": 6}
{"curie": "MONDO:0001994", "names": ["sphenoidal sinus cancer", "cancer of sphenoidal sinus", "malignant sphenoid sinus tumor", "Malignant Sphenoid Sinus Tumor", "malignant sphenoidal sinus tumor", "Malignant Sphenoidal Sinus Tumor", "Malignant Sphenoid Sinus Neoplasm", "Malignant tumor of sphenoid sinus", "malignant sphenoid sinus neoplasm", "Malignant Tumor of Sphenoid Sinus", "malignant tumor of sphenoid sinus", "Malignant tumour of sphenoid sinus", "malignant sphenoidal sinus neoplasm", "malignant tumor of sphenoidal sinus", "Malignant Sphenoidal Sinus Neoplasm", "Malignant Tumor of Sphenoidal Sinus", "malignant tumor of Sphenoidal sinus", "Malignant Neoplasm of Sphenoid Sinus", "Malignant neoplasm of sphenoid sinus", "malignant neoplasm of sphenoid sinus", "Malignant Tumor of the Sphenoid Sinus", "malignant tumor of the sphenoid sinus", "Malignant Neoplasm of Sphenoidal Sinus", "malignant neoplasm of sphenoidal sinus", "Malignant neoplasm of sphenoidal sinus", "malignant tumor of the sphenoidal sinus", "Malignant Tumor of the Sphenoidal Sinus", "malignant neoplasm of the sphenoid sinus", "Malignant Neoplasm of the Sphenoid Sinus", "malignant neoplasm of the sphenoidal sinus", "Malignant Neoplasm of the Sphenoidal Sinus", "Malignant tumor of sphenoid sinus (disorder)", "malignant neoplasm of sphenoid sinus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sphenoidal sinus cancer", "shortest_name_length": 23}
{"curie": "MONDO:0008341", "names": ["McPherson-Hall syndrome", "ptosis strabismus ectopic pupils", "PTOSIS, STRABISMUS, AND ECTOPIC PUPILS", "ptosis, strabismus, and ectopic pupils", "Ptosis, Strabismus, And Ectopic Pupils", "ptosis-strabismus-ectopic pupils syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ptosis-strabismus-ectopic pupils syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0033010", "names": ["EKVP1", "Greither disease", "GREITHER DISEASE", "Greither Disease", "Progressive diffuse PPK", "erythrokeratodermia variabilis", "Transgrediens et progrediens PPK", "erythrokeratodermia, progressive symmetric", "Progressive diffuse palmoplantar keratoderma", "erythrokeratodermia variabilis Et progressiva", "Keratosis extremitatum hereditaria progrediens", "erythrokeratodermia variabilis et progressiva 1", "erythrokeratodermia variabilis ET progressiva 1", "Transgrediens et progrediens palmoplantar keratoderma", "Transgrediens et Progrediens Palmoplantar Keratoderma", "Keratosis palmoplantaris transgrediens et progrediens", "keratosis palmoplantaris transgrediens Et progrediens", "erythrokeratodermia variabilis with erythema Gyratum Repens", "erythrokeratodermia Figurata, congenital familial, in plaques"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythrokeratodermia variabilis et progressiva 1", "shortest_name_length": 5}
{"curie": "UMLS:C4329627", "names": ["Central Nervous System Angiolipoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Angiolipoma", "shortest_name_length": 34}
{"curie": "UMLS:C0151998", "names": ["uterus; spasm", "Uterine spasm", "spasm; uterus", "SPASM UTERINE", "Spasm uterine", "uterine spasm", "UTERINE SPASM", "spasms uterine", "Spasm of uterus", "uterine spasm (diagnosis)", "Spasm of uterus (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine spasm", "shortest_name_length": 13}
{"curie": "UMLS:C4054085", "names": ["Refractory Acute Lymphoblastic Leukemia (ALL)", "Refractory Childhood Acute Lymphoblastic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Childhood Acute Lymphoblastic Leukemia", "shortest_name_length": 45}
{"curie": "UMLS:C4330265", "names": ["Triple hit lymphoma", "Triple Hit Lymphoma", "Triple-Hit Lymphoma", "High-Grade B-Cell Lymphoma with MYC, BCL2, and BCL6 Rearrangements", "High Grade B-Cell Lymphoma with MYC, BCL2, and BCL6 Rearrangements"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Triple hit lymphoma", "shortest_name_length": 19}
{"curie": "MONDO:0000903", "names": ["DYT11", "DYT-SGCE", "Dystonia 11", "dystonia 11", "Myoclonus-Dystonia", "MYOCLONIC DYSTONIA", "myoclonic dystonia", "myoclonus-Dystonia", "Myoclonic dystonia", "Myoclonus dystonia", "myoclonus-dystonia", "DYSTONIA 11, MYOCLONIC", "dystonia-11, myoclonic", "dystonia 11, myoclonic", "dystonia with myoclonus", "Alcohol-responsive dystonia", "MYOCLONUS-DYSTONIA SYNDROME", "Alcohol-Responsive Dystonia", "myoclonus-dystonia syndrome", "Myoclonus-dystonia syndrome", "alcohol-responsive dystonia", "DYSTONIA, ALCOHOL-RESPONSIVE", "dystonia, alcohol-responsive", "Dystonia, Alcohol-Responsive", "dystonia, alcohol responsive", "Myoclonic dystonia (disorder)", "hereditary essential myoclonus", "Hereditary essential myoclonus", "myoclonus, hereditary essential", "MYOCLONUS, HEREDITARY ESSENTIAL", "Myoclonus, hereditary essential"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myoclonus-dystonia syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0278572", "names": ["Skin T-Cell Lymphoma Stage IV", "T-Cell Lymphoma of Skin Stage IV", "Cutaneous T-Cell Lymphoma Stage IV", "stage IV cutaneous T-cell lymphoma", "Cutaneous T-cell lymphoma stage IV", "cutaneous T-cell lymphoma, stage IV", "T-Cell Lymphoma of the Skin Stage IV", "metastatic cutaneous T-cell lymphoma", "cutaneous T-cell lymphoma, metastatic", "stage IV cutaneous T-cell non-Hodgkin lymphoma", "Stage IV Cutaneous T-Cell Non-Hodgkin Lymphoma", "Stage IV Cutaneous T-Cell Non-Hodgkin's Lymphoma", "Stage IV Cutaneous (Skin) T-Cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous T-cell lymphoma stage IV", "shortest_name_length": 29}
{"curie": "MONDO:0002896", "names": ["Primary Syphilis", "Syphilis Primary", "primary syphilis", "Primary syphilis", "SYPHILIS PRIMARY", "Syphilis, primary", "syphilis; primary", "SYPHILIS, PRIMARY", "primary; syphilitic", "Symptomatic early syphilis", "early symptomatic syphilis", "symptomatic early syphilis", "Early symptomatic syphilis", "syphilis early symptomatic", "Primary syphilis (disorder)", "early syphilis, symptomatic", "Early syphilis, symptomatic", "syphilis; early, symptomatic", "primary syphilis (diagnosis)", "early; syphilitic, symptomatic", "Symptomatic early syphilis, NOS", "Early symptomatic syphilis (disorder)", "early symptomatic syphilis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary syphilis", "shortest_name_length": 16}
{"curie": "MONDO:0100054", "names": ["Idiopathic anaphylaxis", "anaphylaxis idiopathic", "idiopathic anaphylaxis", "Idiopathic anaphylaxis (disorder)", "Syndrome of idiopathic anaphylaxis", "idiopathic anaphylaxis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic anaphylaxis", "shortest_name_length": 22}
{"curie": "MONDO:0005426", "names": ["MRI defined brain infarct"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MRI defined brain infarct", "shortest_name_length": 25}
{"curie": "MONDO:0005928", "names": ["Postphlebitic Disease", "venous stress disorder", "Disease, Postphlebitic", "Postphlebitic Syndrome", "Postphlebitic Diseases", "POSTPHLEBITIC SYNDROME", "postphlebitic syndrome", "Postphlebitic syndrome", "syndrome; postphlebitic", "postphlebitic; syndrome", "post-phlebitic syndrome", "Diseases, Postphlebitic", "POST-PHLEBITIC SYNDROME", "Postphlebitic Syndromes", "postthrombotic syndrome", "phlebitic post syndrome", "Post-phlebitic syndrome", "Syndrome, Postphlebitic", "post phlebitic syndrome", "POST PHLEBITIC SYNDROME", "Post phlebitic syndrome", "Postthrombotic syndrome", "Syndromes, Postphlebitic", "post-thrombotic syndrome", "Venous ulcer-leg syndrome", "Postphlebetic syndrome with ulcer", "postphlebetic syndrome with ulcer", "Postphlebitic syndrome (disorder)", "postthrombotic syndrome (diagnosis)", "Post-phlebitic dermatosis of lower leg", "Postphlebetic syndrome with inflammation", "postphlebetic syndrome with inflammation", "Post-phlebitic dermatosis of lower leg (disorder)", "Postphlebetic syndrome with ulcer and inflammation", "postphlebetic syndrome with ulcer and inflammation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "post-thrombotic syndrome", "shortest_name_length": 21}
{"curie": "MONDO:0019245", "names": ["Lipidoses", "lipidosis", "LIPIDOSIS", "Lipidosis", "lipidoses", "lipoidosis", "Lipoidosis", "lipoidoses", "Lipidosis NOS", "Lipidosis, NOS", "Lipoidosis, NOS", "Lipidosis congenital", "lipid storage disease", "lipoid storage diseas", "Lipoid storage diseas", "disease lipid storage", "Lipoidosis (disorder)", "Lipid storage disease", "diseases lipid storage", "storage disease; lipid", "lipid-storage; disease", "lipoid storage disease", "lipid-storage; disorder", "disorder; lipid storage", "disorder; lipid-storage", "lipoid storage disorder", "lipid; storage disorder", "Lipid storage disease, NOS", "Lipoid storage disease NOS", "inborn lipid storage disorder", "inborn error of lipid storage", "Lipid storage disease (disorder)", "lysosomal lipid storage disorder", "rare inborn error of lipid storage", "Lipid storage disorder, unspecified", "Other disorders of lipoid metabolism", "disease (or disorder); lipid-storage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lysosomal lipid storage disorder", "shortest_name_length": 9}
{"curie": "MONDO:0001987", "names": ["Senile brain degen.", "senile brain degeneration", "Senile brain degeneration", "degeneration; brain, senile", "degeneration; senile, brain", "Senile degeneration of brain", "senile degeneration of brain", "Age-related degeneration of brain", "Senile degeneration of brain (disorder)", "senile degeneration of brain (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "senile degeneration of brain", "shortest_name_length": 19}
{"curie": "MONDO:0009988", "names": ["foveal retinoschisis", "Foveal retinoschisis", "RETINOSCHISIS OF FOVEA", "retinoschisis of fovea", "Retinoschisis of Fovea", "familial foveal retinoschisis", "Familial foveal retinoschisis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinoschisis of fovea", "shortest_name_length": 20}
{"curie": "UMLS:C5238463", "names": ["Midgut Neuroendocrine Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Midgut Neuroendocrine Tumor", "shortest_name_length": 27}
{"curie": "UMLS:C1333138", "names": ["Complex Endometrial Hyperplasia with Atypia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Complex Endometrial Hyperplasia with Atypia", "shortest_name_length": 43}
{"curie": "MONDO:0017593", "names": ["JALS", "juvenile ALS", "juvenile Charcot disease", "juvenile ALS (diagnosis)", "Juvenile Charcot disease", "Juvenile Lou Gehrig disease", "juvenile Lou Gehrig disease", "Juvenile amyotrophic lateral sclerosis", "amyotrophic lateral sclerosis juvenile", "juvenile amyotrophic lateral sclerosis", "amyotrophic lateral sclerosis, juvenile", "JALS - juvenile amyotrophic lateral sclerosis", "Juvenile amyotrophic lateral sclerosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile amyotrophic lateral sclerosis", "shortest_name_length": 4}
{"curie": "UMLS:C1699653", "names": ["Anal Mucositis", "Anal mucositis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anal Mucositis", "shortest_name_length": 14}
{"curie": "UMLS:C0854889", "names": ["Pleural mesothelioma malignant advanced", "Advanced Pleural Malignant Mesothelioma", "Malignant Pleural Mesothelioma, Advanced", "Advanced Malignant Mesothelioma of Pleura", "Advanced Malignant Mesothelioma of the Pleura"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pleural mesothelioma malignant advanced", "shortest_name_length": 39}
{"curie": "MONDO:0019027", "names": ["type 2 (Andre syndrome)", "otopalatodigital syndrome", "oto-palato-digital syndrome", "oto-palatal-digital syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "otopalatodigital syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0008724", "names": ["adducted thumbs syndrome", "adducted thumbs-arthrogryposis syndrome, Christian type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adducted thumbs-arthrogryposis syndrome, Christian type", "shortest_name_length": 24}
{"curie": "MONDO:0018644", "names": ["AD-SPG9B", "autosomal dominant complex spastic paraplegia type 9B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant complex spastic paraplegia type 9B", "shortest_name_length": 8}
{"curie": "MONDO:0013881", "names": ["JEB7", "ILNEB", "JEB-RR", "ILNEB syndrome", "congenital NEP syndrome", "congenital ILNEB syndrome", "JEB with respiratory and renal involvement", "JEB with interstitial lung disease and nephrotic syndrome", "junctional epidermolysis bullosa with respiratory and renal involvement", "Interstitial lung disease-nephrotic syndrome-epidermolysis bullosa syndrome", "congenital nephrotic syndrome-epidermolysis bullosa-pulmonary disease syndrome", "congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa", "Congenital nephrotic syndrome, epidermolysis bullosa, pulmonary disease syndrome", "INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL", "interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital", "Junctional epidermolysis bullosa with interstitial lung disease and nephrotic syndrome", "congenital interstitial lung disease-nephrotic syndrome-epidermolysis bullosa syndrome", "Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome", "pidermolysis bullosa, junctional 7, with interstitial lung disease and nephrotic syndrome", "EPIDERMOLYSIS BULLOSA, JUNCTIONAL 7, WITH INTERSTITIAL LUNG DISEASE AND NEPHROTIC SYNDROME", "congenital nephrotic syndrome - interstitial lung disease - epidermolysis bullosa syndrome", "Congenital ILNEB (interstitial lung disease, nephrotic syndrome, epidermolysis bullosa) syndrome", "Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome (disorder)", "Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pidermolysis bullosa, junctional 7, with interstitial lung disease and nephrotic syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C5237420", "names": ["ER and PR Negative Breast Carcinoma", "Hormone Receptor Negative Breast Carcinoma", "Hormone Receptor-Negative Breast Carcinoma", "Hormone Receptor Negative Breast Adenocarcinoma", "Estrogen Receptor and Progesterone Receptor Negative Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hormone Receptor-Negative Breast Carcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C4525088", "names": ["Stage IIB Colorectal Cancer AJCC v8", "Stage IIB Colorectal Carcinoma AJCC v8", "Stage IIB Colorectal (Colon or Rectal) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Colorectal Cancer AJCC v8", "shortest_name_length": 35}
{"curie": "MONDO:0030311", "names": ["COXPD52", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 52", "combined oxidative phosphorylation deficiency 52"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation deficiency 52", "shortest_name_length": 7}
{"curie": "UMLS:C0679401", "names": ["vascular rupture", "Vascular rupture"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vascular rupture", "shortest_name_length": 16}
{"curie": "UMLS:C1527396", "names": ["CYSTIC FIBROSIS PANCREAS", "Cystic fibrosis pancreas", "Mucoviscidosis of pancreas", "Pancreatic Cystic Fibrosis", "CYSTIC FIBROSIS PANCREATIC", "Cystic fibrosis pancreatic", "Cystic fibrosis of pancreas", "cystic fibrosis of pancreas", "Cystic Fibrosis, Pancreatic", "Cystic Fibrosis of Pancreas", "DISEASE FIBROCYSTIC PANCREAS", "Disease fibrocystic pancreas", "Pancreas Fibrocystic Disease", "Pancreas Fibrocystic Diseases", "fibrocystic; disease, pancreas", "disease; fibrocystic, pancreas", "Fibrocystic disease of pancreas", "Cystic fibrosis of the pancreas", "FIBROCYSTIC DISEASE OF PANCREAS", "Fibrocystic Disease of Pancreas", "Fibrocystic disease of the pancreas", "fibrocystic disease of the pancreas", "Cystic fibrosis of pancreas (disorder)", "cystic fibrosis of pancreas (diagnosis)", "disease (or disorder); pancreas, fibrocystic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fibrocystic Disease of Pancreas", "shortest_name_length": 24}
{"curie": "DOID:8651", "names": ["Hodgkin granuloma", "Hodgkin's granuloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's granuloma", "shortest_name_length": 17}
{"curie": "MONDO:0007700", "names": ["HWKS", "HAWKINSINURIA", "hawkinsinuria", "Hawkinsinuria", "4-HPPD deficiency", "Hawkinsinuria (disorder)", "4-Hydroxyphenylpyruvate hydroxylase deficiency", "4-hydroxyphenylpyruvic acid dioxygenase deficiency", "4-alpha-hydroxyphenylpyruvate hydroxylase deficiency", "4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hawkinsinuria", "shortest_name_length": 4}
{"curie": "UMLS:C2986667", "names": ["Stage II Liver Cancer", "stage II adult primary liver cancer", "Stage II Adult Liver Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Adult Liver Cancer AJCC v7", "shortest_name_length": 21}
{"curie": "MONDO:0008748", "names": ["HPS1", "Delta storage pool disease", "DELTA STORAGE POOL DISEASE", "HERMANSKY-PUDLAK SYNDROME 1", "Hermansky-Pudlak syndrome 1", "Hermansky-Pudlak Syndrome 1", "HPS1 Hermansky-Pudlak syndrome", "Hermansky-Pudlak syndrome type 1", "Hermansky-Pudlak syndrome caused by mutation in HPS1", "albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells", "ALBINISM WITH HEMORRHAGIC DIATHESIS AND PIGMENTED RETICULOENDOTHELIAL CELLS", "Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hermansky-Pudlak syndrome 1", "shortest_name_length": 4}
{"curie": "MONDO:0700015", "names": ["chromosome 8 disorder", "Anomaly of chromosome pair 8", "anomaly of chromosome pair 8", "Anomaly of chromosome pair 8, NOS", "Anomaly of chromosome pair 8 (disorder)", "anomaly of chromosome pair 8 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 8 disorder", "shortest_name_length": 21}
{"curie": "MONDO:0024338", "names": ["Mucinous Tumor", "mucinous tumor", "mucinous neoplasm", "Mucinous Neoplasm", "Mucinous neoplasm", "Neoplasm, Mucinous", "Mucinous Neoplasms", "Neoplasms, Mucinous", "tumor; mucinous, unspecified site", "mucinous; tumor, unspecified site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucinous neoplasm", "shortest_name_length": 14}
{"curie": "MONDO:0016047", "names": ["Ophthalmia", "ophthalmia", "Ophthalmias", "OPHTHALMITIS", "Ophthalmitis", "ENDOPHTHALMITIS", "endophthalmitis", "Ophthalmia, NOS", "Endophthalmitis", "Eye inflammation", "Endophthalmitides", "Ophthalmitis, NOS", "Endophthalmitis, NOS", "Endophthalmitis (disorder)", "endophthalmitis (diagnosis)", "eye; disorder, inflammatory", "inflammatory disorder of eye", "Inflammatory disorder of the eye", "inflammatory disorder of eye (diagnosis)", "disease (or disorder); eye, inflammatory", "Inflammatory disorder of the eye (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endophthalmitis", "shortest_name_length": 10}
{"curie": "MONDO:0007918", "names": ["MLCRD", "MCLMR", "Mlcrd syndrome", "MLCRD SYNDROME", "CDMMR SYNDROME", "Cdmmr syndrome", "Microcephaly lymphedema chorioretinal dysplasia", "microcephaly lymphedema chorioretinal dysplasia", "microcephaly-lymphedema-chorioretinopathy syndrome", "Microcephaly-lymphedema-chorioretinopathy syndrome", "Lymphedema, Microcephaly, Chorioretinopathy Syndrome", "lymphedema, microcephaly, chorioretinopathy syndrome", "LYMPHEDEMA, MICROCEPHALY, CHORIORETINOPATHY SYNDROME", "Lymphedema, microcephaly and chorioretinopathy syndrome", "lymphedema, microcephaly and chorioretinopathy syndrome", "MICROCEPHALY, LYMPHEDEMA, CHORIORETINAL DYSPLASIA SYNDROME", "Microcephaly, Lymphedema, Chorioretinal Dysplasia Syndrome", "microcephaly, lymphedema, chorioretinal dysplasia syndrome", "Chorioretinal dysplasia-microcephaly-mental retardation syndrome", "chorioretinal dysplasia-microcephaly-mental retardation syndrome", "lymphedema and retinal folds with ficrocephaly and microphthalmos", "lymphedema and retinal Folds with microcephaly and microphthalmos", "LYMPHEDEMA AND RETINAL FOLDS WITH MICROCEPHALY AND MICROPHTHALMOS", "Lymphedema and Retinal Folds with Microcephaly and Microphthalmos", "chorioretinal dysplasia-microcephaly-intellectual disability syndrome", "microcephaly with or without chorioretinopathy, lymphedema, or mental retardation", "MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION", "microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability", "MICROCEPHALY AND CHORIORETINOPATHY WITH OR WITHOUT MENTAL RETARDATION, AUTOSOMAL DOMINANT", "microcephaly and chorioretinopathy with or without mental retardation, autosomal dominant", "microcephaly and chorioretinopathy with or without intellectual disability, autosomal dominant", "MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR IMPAIRED INTELLECTUAL DEVELOPMENT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability", "shortest_name_length": 5}
{"curie": "MONDO:0001815", "names": ["extrapyramidal and movement disease", "Extrapyramidal and movement disorders", "Extrapyramidal and movement disorders (G20-G26)", "Extrapyramidal and movement disorder, unspecified", "Unspecified extrapyramidal disease and abnormal movement disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extrapyramidal and movement disease", "shortest_name_length": 35}
{"curie": "MONDO:0003539", "names": ["ATLL", "adult t-cell", "adult t cell", "T cell adult ALL", "T Cell Adult ALL", "T-cell adult ALL", "T-Cell Adult ALL", "adult ALL, T-cell", "ALL, adult T-cell", "ALL, adult T cell", "adult ALL, T cell", "T Acute Lymphoblastic Leukemia", "Acute Adult T-cell Leukemia-Lymphoma", "Adult T-Acute Lymphoblastic Leukemia", "Adult T Acute Lymphoblastic Leukemia", "acute Adult T-cell Leukemia-lymphoma", "adult T acute lymphoblastic leukemia", "T-cell adult acute lymphocytic leukemia", "T cell adult acute lymphocytic leukemia", "T-Cell Adult Acute Lymphocytic Leukemia", "leukemia, adult acute lymphocytic T-cell", "adult Precursor T Lymphoblastic Leukemia", "T cell lymphocytic leukemia, acute adult", "T cell acute lymphocytic leukemia, adult", "adult precursor T-lymphoblastic leukemia", "acute lymphocytic leukemia, adult T-cell", "T-cell acute lymphocytic leukemia, adult", "T-cell lymphocytic leukemia, acute adult", "Adult Precursor T-Lymphoblastic Leukemia", "adult acute lymphocytic leukemia, T-cell", "adult precursor T lymphoblastic leukemia", "t-cell adult acute lymphoblastic leukemia", "T-cell adult acute lymphoblastic leukemia", "Adult T-Cell Acute Lymphoblastic Leukemia", "adult T-cell acute lymphoblastic leukemia", "T cell adult acute lymphoblastic leukemia", "T-cell acute lymphoblastic leukemia, adult", "acute lymphoblastic leukemia, adult T-cell", "adult acute lymphoblastic leukemia, T-cell", "T-cell lymphoblastic leukemia, acute adult", "adult acute lymphoblastic leukemia of T cell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-cell adult acute lymphocytic leukemia", "shortest_name_length": 4}
{"curie": "MONDO:0800114", "names": ["follicular bronchiolits"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "follicular bronchiolits", "shortest_name_length": 23}
{"curie": "MONDO:0011016", "names": ["T1D11", "IDDM11", "TYPE 1 DIABETES MELLITUS 11", "type 1 diabetes mellitus 11", "Insulin-Dependent Diabetes Mellitus 11", "insulin-dependent diabetes mellitus 11", "INSULIN-DEPENDENT DIABETES MELLITUS 11", "DIABETES MELLITUS, INSULIN-DEPENDENT, 11", "diabetes mellitus, insulin-dependent, 11", "Diabetes Mellitus, Insulin-Dependent, 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type 1 diabetes mellitus 11", "shortest_name_length": 5}
{"curie": "MONDO:0007870", "names": ["labia minora, incomplete adhesion of", "LABIA MINORA, INCOMPLETE ADHESION OF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "labia minora, incomplete adhesion of", "shortest_name_length": 36}
{"curie": "MONDO:0005217", "names": ["Familial cardiomyopathy", "familial cardiomyopathy", "Cardiomyopathy, familial", "hereditary cardiomyopathy", "Primary familial cardiomyopathy", "Familial cardiomyopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial cardiomyopathy", "shortest_name_length": 23}
{"curie": "OMIM:616060", "names": [], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"]}
{"curie": "MONDO:0034204", "names": ["syndromic congenital sodium diarrhea"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic congenital sodium diarrhea", "shortest_name_length": 36}
{"curie": "MONDO:0011606", "names": ["Baby rattle pelvic dysplasia", "Baby Rattle Pelvis Dysplasia", "baby rattle pelvis dysplasia", "BABY RATTLE PELVIS DYSPLASIA", "baby rattle pelvic dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "baby rattle pelvis dysplasia", "shortest_name_length": 28}
{"curie": "UMLS:C0432526", "names": ["Desmoplastic Trichoepithelioma", "Desmoplastic trichoepithelioma", "Sclerosing epithelial hamartoma", "Sclerosing Epithelial Hamartoma", "Desmoplastic trichoepithelioma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Desmoplastic trichoepithelioma", "shortest_name_length": 30}
{"curie": "UMLS:C0151814", "names": ["coronary occlusion", "occlusion coronary", "Occlusion;coronary", "Coronary occlusion", "Occlusion coronary", "CORONARY OCCLUSION", "Coronary Occlusion", "OCCLUSION, CORONARY", "Coronary Occlusions", "Occlusion, Coronary", "Occlusions, Coronary", "Coronary occlusion NOS", "Coronary occlusion, NOS", "coronary artery occluded", "Coronary artery occluded", "OCCLUSION CORONARY ARTERY", "coronary artery occlusion", "Occlusion coronary artery", "CORONARY ARTERY OCCLUSION", "Coronary artery occlusion", "artery coronary occlusion", "arteries coronary occluded", "coronary (artery) occlusion", "Coronary occlusion (disorder)", "coronary artery occlusion (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Coronary Occlusion", "shortest_name_length": 18}
{"curie": "UMLS:C5207074", "names": ["Penile Epithelioid Hemangioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Penile Epithelioid Hemangioma", "shortest_name_length": 29}
{"curie": "MONDO:0011303", "names": ["FSGS1", "GLOMERULOSCLEROSIS SEGMENTAL", "Segmental glomerulosclerosis", "glomerulosclerosis segmental", "segmental glomerulosclerosis", "Glomerulosclerosis, segmental", "Focal sclerosis with hyalinosis", "focal segmental glomerulosclerosis 1", "FOCAL SEGMENTAL GLOMERULOSCLEROSIS 1", "Focal segmental glomerulosclerosis 1", "Glomerulosclerosis, Focal Segmental, 1", "glomerulosclerosis, focal segmental, 1", "GLOMERULOSCLEROSIS, FOCAL SEGMENTAL, 1", "ACTN4 focal segmental glomerulosclerosis", "focal segmental glomerulosclerosis type 1", "Segmental glomerulosclerosis (morphologic abnormality)", "focal segmental glomerulosclerosis caused by mutation in ACTN4", "familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis", "familial idiopathic steroid-resistant nephrotic syndrome with focal segmental glomerulosclerosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal segmental glomerulosclerosis 1", "shortest_name_length": 5}
{"curie": "MONDO:0004034", "names": ["eye lymphoma", "Eye Lymphoma", "Ocular lymphoma", "Lymphoma of eye", "ocular lymphoma", "Ocular Lymphoma", "lymphoma ocular", "primary eye lymphoma", "Primary Eye Lymphoma", "Primary Ocular Lymphoma", "malignant lymphoma of eye", "Lymphoma of eye (disorder)", "eyeball of camera-type eye lymphoma", "lymphoma of eyeball of camera-type eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eye lymphoma", "shortest_name_length": 12}
{"curie": "MONDO:0000306", "names": ["Trichosporonosis", "trichosporonosis", "Trichosporonoses", "Trichosporon infection", "Trichosporon Infection", "Trichosporon Infections", "Trichosporon; infection", "Infection, Trichosporon", "infection; Trichosporon", "Trichosporonosis (disorder)", "trichosporonosis (diagnosis)", "Trichosporon infectious disease", "Trichosporon disease or disorder", "Trichosporon caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichosporonosis", "shortest_name_length": 16}
{"curie": "UMLS:C0751665", "names": ["Canavan Disease, Sporadic Form", "Sporadic Form of Canavan Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Canavan Disease, Sporadic Form", "shortest_name_length": 30}
{"curie": "UMLS:C0549356", "names": ["INFLICTED INJURY", "Inflicted injury", "inflicted injury", "inflicted injuries"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Inflicted injury", "shortest_name_length": 16}
{"curie": "MONDO:0005460", "names": ["H1N1 Flu", "H1N1 flu", "Swine Flu", "swine flu", "Swine flu", "H1N1 Influenza", "H1N1 influenza", "Swine Influenza", "swine influenza", "influenza A H1N1", "influenza A(H1N1)", "Influenza A (H1N1)", "H1N1 Virus infection", "H1N1 Flu (Swine Flu)", "H1N1 Virus Infection", "Swine influenza virus influenza", "Influenza A (H1N1) Virus infection", "influenza A subtype H1N1 infection", "Influenza A (H1N1) Virus Infection", "Swine influenza virus caused influenza", "influenza A subtype H1N1 infection (diagnosis)", "Influenza due to Influenza A virus subtype H1N1", "Influenza caused by Influenza A virus subtype H1N1", "Influenza caused by Influenza A virus subtype H1N1 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "swine influenza", "shortest_name_length": 8}
{"curie": "UMLS:C0263252", "names": ["Dermatitis due to arnica", "Contact dermatitis due to arnica", "contact dermatitis due to arnica", "Allergic Dermatitis due to Arnica", "Allergic dermatitis due to arnica", "dermatitis due to skin contact with arnica", "contact dermatitis due to arnica (diagnosis)", "Allergic contact dermatitis caused by Arnica", "Allergic contact dermatitis caused by Arnica (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Allergic contact dermatitis caused by Arnica", "shortest_name_length": 24}
{"curie": "MONDO:0032782", "names": ["IMD63", "CD122 DEFICIENCY", "IL2RB DEFICIENCY", "Il2Rb Deficiency", "IL2RB deficiency", "Cd122 Deficiency", "immunodeficiency 63", "Interleukin 2 Receptor, Beta, Deficiency of", "INTERLEUKIN 2 RECEPTOR, BETA, DEFICIENCY OF", "IMMUNODEFICIENCY 63 WITH LYMPHOPROLIFERATION AND AUTOIMMUNITY", "immunodeficiency 63 with lymphoproliferation and autoimmunity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 63 with lymphoproliferation and autoimmunity", "shortest_name_length": 5}
{"curie": "UMLS:C1707546", "names": ["Skin Fibrous Histiocytoma, Histiocytic Variant", "Cutaneous Fibrous Histiocytoma, Histiocytic Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin Fibrous Histiocytoma, Histiocytic Variant", "shortest_name_length": 46}
{"curie": "MONDO:0008250", "names": ["IGHD2", "IGHD 2", "IGHD II", "congenital IGHD type II", "Congenital IGHD type II", "isolated growth hormone deficiency type 2", "congenital isolated GH deficiency type II", "Congenital isolated GH deficiency type II", "isolated growth hormone deficiency type II", "isolated Growth hormone deficiency, type 2", "Isolated growth hormone deficiency type II", "isolated growth hormone deficiency, type II", "ISOLATED GROWTH HORMONE DEFICIENCY, TYPE II", "Isolated Growth Hormone Deficiency, Type II", "growth hormone deficiency, isolated, type II", "Autosomal dominant isolated somatotropin deficiency", "Congenital isolated growth hormone deficiency type II", "congenital isolated growth hormone deficiency type II", "autosomal dominant isolated growth hormone deficiency", "Growth hormone deficiency, isolated autosomal dominant", "GROWTH HORMONE DEFICIENCY, ISOLATED, AUTOSOMAL DOMINANT", "Growth hormone deficiency, isolated, autosomal dominant", "Isolated growth hormone deficiency - autosomal dominant", "Growth Hormone Deficiency, Isolated, Autosomal Dominant", "Isolated growth hormone deficiency - autosomal dominant (disorder)", "autosomal dominant pituitary dwarfism due to isolated growth hormone deficiency", "pituitary dwarfism due to isolated growth hormone deficiency autosomal dominant", "pituitary dwarfism due to isolated Growth hormone deficiency, autosomal dominant", "PITUITARY DWARFISM DUE TO ISOLATED GROWTH HORMONE DEFICIENCY, AUTOSOMAL DOMINANT", "Pituitary Dwarfism Due To Isolated Growth Hormone Deficiency, Autosomal Dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated growth hormone deficiency type II", "shortest_name_length": 5}
{"curie": "UMLS:C4682636", "names": ["Primary Peritoneal Cancer by AJCC v8 Stage", "Primary Peritoneal Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Peritoneal Cancer by AJCC v8 Stage", "shortest_name_length": 42}
{"curie": "MONDO:0006277", "names": ["lymphangiomyomatosis", "lymphangioleiomyomatosis", "Lung Lymphangiomyomatosis", "lung lymphangiomyomatosis", "lung lymphangioleiomyomatosis", "Lung Lymphangioleiomyomatosis", "pulmonary lymphangiomyomatosis", "pulmonary lymphangioleiomyomatosis", "Pulmonary lymphangioleiomyomatosis", "Pulmonary lymphangioleiomyomatosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung lymphangioleiomyomatosis", "shortest_name_length": 20}
{"curie": "OMIM:615311", "names": ["BMND17", "BONE MINERAL DENSITY, LOW, SUSCEPTIBILITY TO", "BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 17"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 6}
{"curie": "UMLS:C0178540", "names": ["Cerebral Ischemia Hypoxia", "Cerebral Hypoxia-Ischemia", "Cerebral Hypoxia Ischemia", "cerebral ischemia/hypoxia", "Cerebral Ischemia-Hypoxia", "Cerebral Hypoxia-Ischemias", "Ischemia-Hypoxia, Cerebral", "Cerebral Ischemia-Hypoxias", "Ischemia Hypoxia, Cerebral", "Hypoxia Ischemia, Cerebral", "Hypoxia-Ischemia, Cerebral", "Ischemia-Hypoxias, Cerebral", "Hypoxia-Ischemias, Cerebral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebral Hypoxia-Ischemia", "shortest_name_length": 25}
{"curie": "UMLS:C4683603", "names": ["Lugano Classification Stage IV Childhood Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage IV Childhood Hodgkin Lymphoma AJCC v8", "shortest_name_length": 65}
{"curie": "MONDO:0007905", "names": ["LIP, HAMARTOMATOUS", "Lip, Hamartomatous", "lip, hamartomatous", "ENLARGEMENT OF LOWER LIP", "enlargement of Lower lip", "Enlargement of Lower Lip"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lip, hamartomatous", "shortest_name_length": 18}
{"curie": "UMLS:C1333854", "names": ["Grade 4 Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade 4 Malignant Neoplasm", "shortest_name_length": 26}
{"curie": "MONDO:0056816", "names": ["vulvar Neuroendocrine cancer", "Vulvar Neuroendocrine Cancer", "Vulvar Neuroendocrine Carcinoma", "vulvar neuroendocrine carcinoma", "vulvar Neuroendocrine carcinoma", "mammalian vulva neuroendocrine carcinoma", "vulvar high grade Neuroendocrine neoplasm", "Vulvar High Grade Neuroendocrine Neoplasm", "Vulvar High Grade Neuroendocrine Carcinoma", "vulvar high grade Neuroendocrine carcinoma", "neuroendocrine carcinoma of mammalian vulva"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar neuroendocrine carcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0010366", "names": ["FGS5", "FG syndrome 5", "Fg Syndrome 5", "FG SYNDROME 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FG syndrome 5", "shortest_name_length": 4}
{"curie": "MONDO:0032763", "names": ["IMD62", "IMMUNODEFICIENCY 62", "immunodeficiency 62"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 62", "shortest_name_length": 5}
{"curie": "MONDO:0033308", "names": ["JBTS30", "JOUBERT SYNDROME 30", "Joubert syndrome 30"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome 30", "shortest_name_length": 6}
{"curie": "MONDO:0017560", "names": ["Back knee", "Genu recurvata", "genu recurvatum", "Genu recurvatum", "Genu Recurvatum", "recurvatum; genu", "genu; recurvatum", "Knee hyperextension", "congenital genu recurvatum", "Congenital genu recurvatum", "genu; recurvatum, congenital", "knee deformity genu recurvatum", "Hyperextension of Knee Deformity", "Hyperextension Deformity of Knee", "hyperextension of knee deformity", "Hyperextension deformity of knee", "hyperextension deformity of knee", "genu recurvatum (physical finding)", "Congenital genu recurvatum (disorder)", "congenital genu recurvatum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital genu recurvatum", "shortest_name_length": 9}
{"curie": "MONDO:0013164", "names": ["UPB1D", "BETA-ureidopropionase deficiency", "beta-ureidopropionase deficiency", "Beta-alanine synthase deficiency", "BETA-UREIDOPROPIONASE DEFICIENCY", "Beta-Ureidopropionase Deficiency", "Beta-ureidopropionase deficiency", "Deficiency of beta-ureidopropionase", "Deficiency of beta-ureidopropionase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "beta-ureidopropionase deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C5668297", "names": ["Advanced Malignant Abdominal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Malignant Abdominal Neoplasm", "shortest_name_length": 37}
{"curie": "UMLS:C0276908", "names": ["P carinii Infection", "P carinii Infections", "P. carinii Infection", "Infection, P carinii", "P. carinii Infections", "P jirovecii Infection", "Infection, P. carinii", "P jirovecii Infections", "Infection, P jirovecii", "P. jirovecii Infection", "Infection, P. jirovecii", "P. jirovecii Infections", "Pneumocystis carinii Infection", "Pneumocystis jiroveci infection", "Pneumocystis jirovecii infection", "Pneumocystis jirovecii Infection", "Infection, Pneumocystis jirovecii", "Pneumocystis jirovecii Infections", "Infection by Pneumocystis jiroveci", "Infection by Pneumocystis jirovecii", "Infection caused by Pneumocystis jirovecii", "Infection by Pneumocystis jirovecii (disorder)", "Infection caused by Pneumocystis jirovecii (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infection by Pneumocystis jirovecii (disorder)", "shortest_name_length": 19}
{"curie": "MONDO:0007091", "names": ["Amelia and Terminal Transverse Hemimelia", "AMELIA AND TERMINAL TRANSVERSE HEMIMELIA", "amelia and terminal transverse hemimelia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amelia and terminal transverse hemimelia", "shortest_name_length": 40}
{"curie": "UMLS:C0752205", "names": ["secondary dystonia", "Secondary Dystonia", "Dystonia, Secondary", "Secondary Dystonias", "Dystonias, Secondary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dystonia, Secondary", "shortest_name_length": 18}
{"curie": "UMLS:C0279599", "names": ["TdT negative adult ALL", "adult ALL, TdT negative", "TdT negative ALL, adult", "ALL, adult TdT negative", "ALL, TdT negative, adult", "TdT Negative Acute Lymphoblastic Leukemia", "TdT negative adult acute lymphocytic leukemia", "leukemia, adult acute lymphocytic TdT negative", "TdT negative acute lymphocytic leukemia, adult", "TdT negative lymphocytic leukemia, acute adult", "acute lymphocytic leukemia, adult TdT negative", "Adult TdT Negative Acute Lymphoblastic Leukemia", "TdT negative adult acute lymphoblastic leukemia", "acute lymphoblastic leukemia, adult TdT negative"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult TdT Negative Acute Lymphoblastic Leukemia", "shortest_name_length": 22}
{"curie": "UMLS:C2828030", "names": ["Stage IB Skin Melanoma AJCC v7", "Stage IB Cutaneous (Skin) Melanoma", "Stage IB Cutaneous Melanoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Cutaneous Melanoma AJCC v7", "shortest_name_length": 30}
{"curie": "MONDO:0021370", "names": ["Minor Salivary Gland Tumor", "minor salivary gland tumor", "Minor Salivary Gland Neoplasm", "tumor of minor salivary gland", "minor salivary gland neoplasm", "Tumor of Minor Salivary Gland", "Tumor of minor salivary gland", "Tumour of minor salivary gland", "Neoplasm of Minor Salivary Gland", "Neoplasm of minor salivary gland", "neoplasm of minor salivary gland", "Tumor of the Minor Salivary Gland", "tumor of the minor salivary gland", "Neoplasm of the Minor Salivary Gland", "neoplasm of the minor salivary gland", "minor salivary gland neoplasm (disease)", "Neoplasm of minor salivary gland (disorder)", "neoplasm of minor salivary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplasm of minor salivary gland", "shortest_name_length": 26}
{"curie": "MONDO:0017769", "names": ["acquired immunodeficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired immunodeficiency", "shortest_name_length": 25}
{"curie": "MONDO:0004570", "names": ["volvulus", "VOLVULUS", "Volvulus", "bowel torsion", "bowel; torsion", "torsion; bowel", "bowel volvulus", "Torsion of bowel", "Volvulus of bowel", "intestine volvulus", "volvulus of midgut", "INTESTINE VOLVULUS", "intestinal volvulus", "Intestinal volvulus", "Volvulus, Intestine", "Intestinal Volvulus", "INTESTINAL VOLVULUS", "Volvulus, Intestinal", "volvulus (diagnosis)", "Obstruction by torsion", "Obstruction by kinking", "Obstruction by twisting", "Intestinal volvulus, NOS", "Obstruction by kinking, NOS", "Obstruction by torsion, NOS", "Obstruction by twisting, NOS", "Intestinal volvulus (disorder)", "familial intestinal malrotation", "Twist of intestine, bowel, or colon", "twist of intestine, bowel, or colon", "Torsion of intestine, bowel, or colon", "Knotting of intestine, bowel, or colon", "Twisting of intestine on mesenteric axis", "Strangulation of intestine, bowel, or colon", "Obstruction by torsion (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intestinal volvulus", "shortest_name_length": 8}
{"curie": "MONDO:0009284", "names": ["GSSDE", "glutathione synthetase deficiency of erythrocytes", "Glutathione synthetase deficiency without 5-oxoprolinuria", "glutathione synthetase deficiency without 5-oxoprolinuria", "hemolytic anemia due to glutathione synthetase deficiency", "glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to", "Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to", "GLUTATHIONE SYNTHETASE DEFICIENCY OF ERYTHROCYTES, HEMOLYTIC ANEMIA DUE TO", "[OBSOLETE] Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glutathione synthetase deficiency without 5-oxoprolinuria", "shortest_name_length": 5}
{"curie": "MONDO:0006213", "names": ["mouth floor mucoepidermoid carcinoma", "floor of mouth mucoepidermoid carcinoma", "Floor of Mouth Mucoepidermoid Carcinoma", "Mucoepidermoid Carcinoma of Floor of Mouth", "mucoepidermoid carcinoma of floor of mouth", "Mucoepidermoid Carcinoma of the Floor of Mouth", "mucoepidermoid carcinoma of the floor of mouth", "mucoepidermoid carcinoma of floor of mouth (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "floor of mouth mucoepidermoid carcinoma", "shortest_name_length": 36}
{"curie": "UMLS:C0349554", "names": ["VIN I", "vin i", "VAIN 1", "VAIN I", "vain i", "VAIN Grade 1", "Vaginal LSIL", "Low Grade VAIN", "mild vaginal dysplasia", "Mild vaginal dysplasia", "mild vaginal dysplasia (diagnosis)", "Grade I Vaginal Intraepithelial Neoplasia", "Vaginal intraepithelial neoplasia grade 1", "Vaginal Intraepithelial Neoplasia Grade 1", "Grade 1 Vaginal Intraepithelial Neoplasia", "Vaginal intraepithelial neoplasia grade I", "VAIN - Vaginal intraepithelial neoplasia 1", "vagina; intraepithelial neoplasia, grade I", "Low Grade Vaginal Intraepithelial Neoplasia", "neoplasia; intraepithelial, vagina, grade I", "Intraepithelial Neoplasia of Vagina Grade 1", "Intraepithelial Neoplasia of the Vagina Grade 1", "Vaginal low grade squamous intraepithelial lesion", "Vaginal intraepithelial neoplasia [VAIN], grade I", "Low-Grade Vaginal Squamous Intraepithelial Lesion", "Low Grade Vaginal Squamous Intraepithelial Lesion", "Vaginal Low-Grade Squamous Intraepithelial Lesion", "Vaginal Low Grade Squamous Intraepithelial Lesion", "Vaginal intraepithelial neoplasia grade 1 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal intraepithelial neoplasia grade 1", "shortest_name_length": 5}
{"curie": "MONDO:0032724", "names": ["SEMDJL3", "spondyloepimetaphyseal dysplasia with joint laxity type 3", "spondyloepimetaphyseal dysplasia with joint laxity, type 3", "SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepimetaphyseal dysplasia with joint laxity, type 3", "shortest_name_length": 7}
{"curie": "UMLS:C0392519", "names": ["Calcium deficiency", "calcium deficiency", "CALCIUM DEFICIENCY", "deficiency; calcium", "calcium; deficiency", "calcium deficiencies", "Calcium deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Calcium deficiency", "shortest_name_length": 18}
{"curie": "MONDO:0008320", "names": ["Otto pelvis", "Pelvis, Otto", "otto's pelvis", "Otto's pelvis", "otto's disease", "Otto's disease", "Arthrokatadysis", "Chroback's pelvis", "Protrusio acetabuli", "protrusio acetabuli", "PROTRUSIO ACETABULI", "PROTRUSIO acetabuli", "Protrusio acetabulae", "Protrusio acetabularis", "Otto's pelvis (disorder)", "Otto's disease or pelvis", "Protrusio acetabuli, NOS", "Protrusio acetabuli (disease)", "Abnormally indented hip sockets", "Intrapelvic protrusion of acetabulum", "intrapelvic protrusion of acetabulum", "Intrapelvic protrusion of acetabulum, NOS", "Intrapelvic protrusion of acetabulum (disorder)", "intrapelvic protrusion of acetabulum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Protrusio acetabuli", "shortest_name_length": 11}
{"curie": "UMLS:C0279594", "names": ["non-T, non-B adult ALL", "non T, non B adult ALL", "adult ALL, non-T, non-B", "adult ALL, non T, non B", "ALL, adult non T, non B", "non T, non B ALL, adult", "non-T, non-B ALL, adult", "ALL, adult non-T, non-B", "ALL, non T, non B, adult", "ALL, non-T, non-B, adult", "leukemia, adult ALL non-T, non-B", "Non-T Non-B Acute Lymphoblastic Leukemia", "non-T, non-B adult acute lymphocytic leukemia", "non-B, non-T adult acute lymphocytic leukemia", "non T, non B adult acute lymphocytic leukemia", "non B, non T adult acute lymphocytic leukemia", "adult acute lymphocytic leukemia, non-T, non-B", "non-T, non-B lymphocytic leukemia, acute adult", "Adult Non-T Non-B Acute Lymphoblastic Leukemia", "non T, non B acute lymphocytic leukemia, adult", "non T, non B lymphocytic leukemia, acute adult", "leukemia, adult acute lymphocytic non-T, non-B", "acute lymphocytic leukemia, adult non-T, non-B", "non-T, non-B acute lymphocytic leukemia, adult", "non-T, non-B adult acute lymphoblastic leukemia", "acute lymphoblastic leukemia, adult non-T, non-B", "adult acute lymphoblastic leukemia, non-T, non-B", "non-T, non-B lymphoblastic leukemia, acute adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Non-T Non-B Acute Lymphoblastic Leukemia", "shortest_name_length": 22}
{"curie": "MONDO:0018768", "names": ["FCU", "FCAS", "COLD HYPERSENSITIVITY", "Familial Cold Urticaria", "familial cold urticaria", "Familial cold urticaria", "Cold Urticaria, Familial", "Familial Cold Urticarias", "COLD URTICARIA, FAMILIAL", "Urticaria, Familial Cold", "FCU - familial cold urticaria", "Familial cold urticaria (disorder)", "familial polymorphous cold eruption", "Familial Cold Autoinflammatory Syndrome", "Familial cold autoinflammatory syndrome", "familial cold autoinflammatory syndrome", "FCAS - familial cold autoinflammatory syndrome", "familial cold autoinflammatory syndrome (FCAS)", "Familial Cold Induced Autoinflammatory Syndrome", "Familial Cold-Induced Autoinflammatory Syndrome", "Cold-Induced Autoinflammatory Syndrome, Familial", "COLD-INDUCED AUTOINFLAMMATORY SYNDROME, FAMILIAL", "Cold Induced Autoinflammatory Syndrome, Familial", "familial cold autoinflammatory syndrome (FCAS) (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial cold autoinflammatory syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C4764217", "names": ["Refractory Adrenal Gland Pheochromocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Adrenal Gland Pheochromocytoma", "shortest_name_length": 41}
{"curie": "MONDO:0009777", "names": ["OLIVER SYNDROME", "Oliver Syndrome", "Oliver syndrome", "postaxial polydactyly and mental retardation", "POSTAXIAL POLYDACTYLY AND MENTAL RETARDATION", "Postaxial Polydactyly and Mental Retardation", "postaxial polydactyly and intellectual disability", "postaxial polydactyly-intellectual disability syndrome", "Postaxial polydactyly-intellectual disability syndrome", "Postaxial polydactyly and intellectual disability syndrome", "postaxial polydactyly and intellectual disability syndrome", "Postaxial polydactyly and intellectual disability syndrome (disorder)", "postaxial polydactyly and intellectual disability syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oliver syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0012520", "names": ["IRAN, TYPE A", "IRAN, Type A", "Iran, type a", "insulin resistance type A", "Type A insulin resistance", "insulin resistance, type A", "Insulin resistance - type A", "type A insulin resistance syndrome", "Type A Insulin Resistance Syndrome", "insulin-resistance syndrome type A", "Insulin-resistance syndrome type A", "Insulin resistance syndrome, type A", "Insulin resistance - type A (disorder)", "insulin resistance, type A (diagnosis)", "Insulin-resistant acanthosis nigricans type A", "insulin-resistant acanthosis nigricans, type A", "Hereditary benign acanthosis nigricans with insulin resistance", "DIABETES MELLITUS, INSULIN-RESISTANT, WITH ACANTHOSIS NIGRICANS", "diabetes mellitus, insulin-resistant, with acanthosis nigricans", "Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans", "Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans, Type A", "DIABETES MELLITUS, INSULIN-RESISTANT, WITH ACANTHOSIS NIGRICANS, TYPE A", "diabetes mellitus, insulin-resistant, with acanthosis nigricans, type a", "Hereditary benign acanthosis nigricans with insulin resistance (disorder)", "insulin resistant diabetes mellitus with acanthosis nigricans and hyperandrogenism", "Insulin Resistant Diabetes Mellitus with Acanthosis Nigricans and Hyperandrogenism", "Insulin Receptor Defect with Insulin-Resistant Diabetes Mellitus and Acanthosis Nigricans", "Insulin receptor defect with insulin-resistant diabetes mellitus and acanthosis nigricans", "insulin receptor, defect in, with insulin-resistant diabetes mellitus and acanthosis nigricans", "INSULIN RECEPTOR, DEFECT IN, WITH INSULIN-RESISTANT DIABETES MELLITUS AND ACANTHOSIS NIGRICANS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "insulin-resistance syndrome type A", "shortest_name_length": 12}
{"curie": "MONDO:0013726", "names": ["EMPF", "EMPF1", "ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 1", "encephalopathy due to defective mitochondrial and peroxisomal fission 1", "lethal encephalopathy due to mitochondrial and peroxisomal fission defect", "encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 1", "encephalopathy, lethal, due to defective mitochondrial and peroxisomal fission", "ENCEPHALOPATHY, LETHAL, DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION", "DNM1L-related encephalopathy due to mitochondrial and peroxisomal fission defect", "DNM1L-associated encephalopathy due to peroxisomal and mitochondrial fission defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 1", "shortest_name_length": 4}
{"curie": "MONDO:0024414", "names": ["Anaerobic cellulitis", "anaerobic cellulitis", "cellulitis anaerobic", "CELLULITIS, ANAEROBIC", "anaerobic; cellulitis", "cellulitis; anaerobic", "Anaerobic cellulitis (disorder)", "Anaerobic cellulitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anaerobic cellulitis", "shortest_name_length": 20}
{"curie": "MONDO:0021429", "names": ["floor of mouth scc", "Floor of Mouth SCC", "SCC of Floor of Mouth", "scc of floor of mouth", "scc of the floor of mouth", "SCC of the Floor of Mouth", "mouth floor squamous cell carcinoma", "Floor of Mouth Squamous Cell Carcinoma", "floor of mouth squamous cell carcinoma", "squamous cell carcinoma of floor of mouth", "Squamous cell carcinoma of floor of mouth", "Squamous Cell Carcinoma of Floor of Mouth", "MOUTH FLOOR CANCER SQUAMOUS CELL CARCINOMA", "squamous cell carcinoma of the floor of mouth", "Squamous Cell Carcinoma of the Floor of Mouth", "SCC - Squamous cell carcinoma of floor of mouth", "Squamous cell carcinoma of floor of mouth (disorder)", "squamous cell carcinoma of floor of mouth (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "squamous cell carcinoma of floor of mouth", "shortest_name_length": 18}
{"curie": "UMLS:C5203813", "names": ["Endometrioid Adenocarcinoma, Variant with Squamous Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endometrioid Adenocarcinoma, Variant with Squamous Differentiation", "shortest_name_length": 66}
{"curie": "UMLS:C1709454", "names": ["Pancreatic Endocrine Microadenoma", "Pancreatic Neuroendocrine Microtumor", "Pancreatic Neuroendocrine Microadenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Neuroendocrine Microtumor", "shortest_name_length": 33}
{"curie": "MONDO:0012433", "names": ["SLSN6", "Senior-Loken Syndrome 6", "Senior-Loken syndrome 6", "SENIOR-LOKEN SYNDROME 6", "SENIOR-Loken syndrome 6", "Senior-Loken syndrome type 6", "CEP290 Senior-Loken syndrome", "Senior-Loken syndrome caused by mutation in CEP290"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Senior-Loken syndrome 6", "shortest_name_length": 5}
{"curie": "MONDO:0020404", "names": ["shone complex", "Shone complex", "shone syndrome", "Shone syndrome", "Shone Syndrome", "Shone's syndrome", "Shone complex (disorder)", "Shone's Syndrome (Greater than 3 Sites)", "shone's syndrome (greater than 3 sites)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "shone complex", "shortest_name_length": 13}
{"curie": "UMLS:C5419744", "names": ["Cutaneous Perineurioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous Perineurioma", "shortest_name_length": 22}
{"curie": "UMLS:C4725023", "names": ["Recurrent Mixed Phenotype Acute Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Mixed Phenotype Acute Leukemia", "shortest_name_length": 40}
{"curie": "MONDO:0011025", "names": ["ATCAY", "CAYMAN ATAXIA", "Cayman ataxia", "Cayman cerebellar ataxia", "Cayman type cerebellar ataxia", "Cerebellar ataxia Cayman type", "cerebellar ataxia, CAYMAN type", "Cerebellar Ataxia, Cayman Type", "CEREBELLAR ATAXIA, CAYMAN TYPE", "cerebellar ataxia, Cayman type", "Cerebellar ataxia, Cayman type", "ataxia, cerebellar, Cayman type", "Cerebellar ataxia Cayman type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cayman type cerebellar ataxia", "shortest_name_length": 5}
{"curie": "UMLS:C4763626", "names": ["Peripheral Hemangioblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peripheral Hemangioblastoma", "shortest_name_length": 27}
{"curie": "MONDO:0004414", "names": ["Tamoxifen-Related Endometrial Lesion", "tamoxifen-related endometrial lesion", "Tamoxifen-Related Endometrial Disorder", "tamoxifen-related endometrial disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tamoxifen-related endometrial lesion", "shortest_name_length": 36}
{"curie": "UMLS:C4725842", "names": ["Localized Cerebral Neoplasm", "Non-Metastatic Cerebral Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized Cerebral Neoplasm", "shortest_name_length": 27}
{"curie": "UMLS:C5670553", "names": ["Metastatic Prostate Adenocarcinoma with Neuroendocrine Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Prostate Adenocarcinoma with Neuroendocrine Differentiation", "shortest_name_length": 70}
{"curie": "MONDO:0004982", "names": ["Pancreatitis", "pancreatitis", "PANCREATITIS", "Pancreatitis NOS", "Pancreatitis, NOS", "Pancreas inflamed", "pancreas inflammation", "pancreas Inflammation", "Pancreatitis (disorder)", "Pancreatic inflammation", "pancreatitis (diagnosis)", "inflammation of pancreas", "Inflammation of pancreas", "Inflammatory Pancreatic Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatitis", "shortest_name_length": 12}
{"curie": "MONDO:0019470", "names": ["ANKL", "ANKCL", "NK cell leukemia", "NK-Cell Leukemia", "NK Cell Leukemia", "NK-cell leukemia", "NK-cell leukaemia", "NK-cell LGL leukemia", "aggressive NK-cell leukemia", "leukemia aggressive NK-cell", "Aggressive NK-Cell Leukemia", "Aggressive NK cell leukemia", "aggressive NK-cell lymphoma", "aggressive NK cell leukemia", "Aggressive NK-cell lymphoma", "Aggressive NK-cell leukemia", "Aggressive NK-cell leukaemia", "natural Killer cell leukemia", "natural killer cell leukemia", "aggressive NK-cell leukaemia", "Aggressive NK cell leukaemia", "Natural killer-cell leukemia", "Natural Killer Cell Leukemia", "Natural killer-cell leukaemia", "natural killer cell leukaemia", "aggressive NK-cell leukemia/lymphoma", "Aggressive NK-Cell Leukemia/Lymphoma", "natural killer cell leukemia (disease)", "Aggressive natural killer-cell leukemia", "aggressive NK-cell leukemia (diagnosis)", "aggressive natural killer cell leukemia", "Aggressive natural killer-cell leukaemia", "leukemia (disease) of natural killer cell", "NK-cell large granular lymphocyte leukemia", "large granular Lymphocyte Leukemia, NK-cell type", "large granular lymphocyte leukemia, NK-cell type", "Aggressive natural killer-cell leukemia (disorder)", "Aggressive natural killer-cell leukemia (diagnosis)", "aggressive NK-cell leukemia (morphologic abnormality)", "leukemia lymphocytic acute (all) aggressive natural killer-cell", "Aggressive natural killer-cell leukemia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aggressive NK-cell leukemia", "shortest_name_length": 4}
{"curie": "UMLS:C4552680", "names": ["Stage I Thyroid Gland Medullary Cancer", "Stage I Thyroid Gland Medullary Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Thyroid Gland Medullary Carcinoma AJCC v8", "shortest_name_length": 38}
{"curie": "UMLS:C3887516", "names": ["Brain Stem Mixed Glioma", "childhood brainstem mixed glioma", "mixed glioma, childhood brainstem", "childhood brain stem mixed glioma", "Childhood Brain Stem Mixed Glioma", "mixed glioma, childhood brain stem"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Brain Stem Mixed Glioma", "shortest_name_length": 23}
{"curie": "UMLS:C4521634", "names": ["Stage IVA Laryngeal Throat Cancer", "Stage IVA Laryngeal Cancer AJCC v8", "Stage IVA Laryngeal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Laryngeal Cancer AJCC v8", "shortest_name_length": 33}
{"curie": "MONDO:0009200", "names": ["eyebrow duplication-syndactyly syndrome", "eyebrows duplication of, with stretchable skin and syndactyly", "Eyebrows duplication of, with stretchable skin and syndactyly", "Eyebrows, Duplication of, with Stretchable Skin and Syndactyly", "EYEBROWS, DUPLICATION OF, WITH STRETCHABLE SKIN AND SYNDACTYLY", "eyebrows, DUPLICATION of, with stretchable skin and syndactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eyebrow duplication-syndactyly syndrome", "shortest_name_length": 39}
{"curie": "MONDO:0800144", "names": ["autoimmune pulmonary disease due to PD-1 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune pulmonary disease due to PD-1 deficiency", "shortest_name_length": 51}
{"curie": "MONDO:0037829", "names": ["Purine Disorder", "purine metabolism disease", "Purine metabolism disorder", "purine metabolism disorder", "metabolic disorder; purine", "purine; metabolic disorder", "disorder of purine metabolism", "Disorder of purine metabolism", "Disorders of purine metabolism", "DISORDERS OF PURINE METABOLISM", "disorders of purine metabolism", "Purine metabolism disorder NOS", "Disorder of purine metabolism, NOS", "Disorder of purine metabolism (disorder)", "disorders of purine metabolism (diagnosis)", "purine nucleobase metabolic process disease", "disorder of purine nucleobase metabolic process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "purine metabolism disease", "shortest_name_length": 15}
{"curie": "UMLS:C1707675", "names": ["Densely Granulated Somatotroph PitNET/Adenoma", "Densely Granulated Pituitary Gland Somatotroph Adenoma", "Densely Granulated Somatotroph Pituitary Neuroendocrine Tumor", "Densely Granulated Somatotroph Pituitary Neuroendocrine Tumor/Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Densely Granulated Somatotroph Pituitary Neuroendocrine Tumor", "shortest_name_length": 45}
{"curie": "MONDO:0020162", "names": ["secondary ectropion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary ectropion", "shortest_name_length": 19}
{"curie": "MONDO:0007295", "names": ["ECT", "BRE", "BECTS", "BECRS", "BCECTS", "sylvan seizures", "epilepsy roland", "Rolands Epilepsy", "Sylvian Epilepsy", "rolandic epilepsy", "Rolandic epilepsy", "Rolandic Epilepsy", "Epilepsy, Rolands", "Epilepsy, Sylvian", "Epilepsy, Rolandic", "Rolandic Epilepsies", "Epilepsies, Rolandic", "Centrotemporal Epilepsy", "CENTRALOPATHIC EPILEPSY", "centralopathic epilepsy", "Centralopathic epilepsy", "CENTROTEMPORAL EPILEPSY", "Centrotemporal epilepsy", "Centralopathic Epilepsy", "centrotemporal epilepsy", "benign Rolandic epilepsy", "Benign rolandic epilepsy", "benign rolandic epilepsy", "Benign Rolandic Epilepsy", "Epilepsy, Centralopathic", "Benign Rolandic epilepsy", "BENIGN ROLANDIC EPILEPSY", "Epilepsy, Centrotemporal", "Centralopathic Epilepsies", "Centrotemporal Epilepsies", "Rolandic Epilepsy, Benign", "Epilepsy, Benign Rolandic", "Epilepsies, Centralopathic", "Epilepsies, Centrotemporal", "benign Rolandic epilepsy (BRE)", "Temporal-central focal epilepsy", "TEMPORAL-CENTRAL FOCAL EPILEPSY", "Temporal Central Focal Epilepsy", "temporal-central focal epilepsy", "Temporal-Central Focal Epilepsy", "Epilepsy, Temporal-Central Focal", "Focal Epilepsy, Temporal-Central", "Temporal-Central Focal Epilepsies", "Epilepsies, Temporal-Central Focal", "Focal Epilepsies, Temporal-Central", "Benign Rolandic epilepsy (disorder)", "benign Rolandic epilepsy (diagnosis)", "Benign Rolandic Epilepsy of Childhood", "centrotemporal epilepsy, isolated cases", "benign epilepsy with centrotemporal spikes", "Benign Epilepsy With Centrotemporal Spikes", "benign Rolandic epilepsy of childhood (BREC)", "childhood epilepsy with centrotemporal spikes", "Benign childhood epilepsy with centrotemporal spike", "benign epilepsy with centro-temporal spikes (BECTS)", "benign childhood epilepsy with centrotemporal spike", "Benign Childhood Epilepsy With Centrotemporal Spikes", "Benign Childhood Epilepsy with Centrotemporal Spikes", "benign childhood epilepsy with centrotemporal spikes", "Benign Childhood Epilepsy With Centro Temporal Spikes", "Benign Childhood Epilepsy With Centro-Temporal Spikes", "Benign Epilepsy Of Childhood With Centrotemporal Spikes", "Benign epilepsy of childhood with centrotemporal spikes", "benign epilepsy of childhood with centrotemporal spikes", "BENIGN EPILEPSY OF CHILDHOOD WITH CENTROTEMPORAL SPIKES", "Benign familial epilepsy of childhood with rolandic spikes", "benign familial epilepsy of childhood with rolandic spikes", "benign epilepsy of childhood with centrotemporal spikes (BECCT)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood epilepsy with centrotemporal spikes", "shortest_name_length": 3}
{"curie": "MONDO:0014301", "names": ["DDD3", "Dowling-Degos disease 3", "dowling-degos disease 3", "DOWLING-DEGOS DISEASE 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dowling-degos disease 3", "shortest_name_length": 4}
{"curie": "MONDO:0025263", "names": ["equine Strongyloses", "Equine Strongylosis", "Equine Strongyloses", "equine Strongylosis", "Strongylosis, Equine", "Strongylosis, equine", "Strongyloses, equine", "Strongyloses, Equine", "equine strongyle infection", "Equine Strongyle Infection", "strongyle infection, equine", "equine strongyle infections", "Equine Strongyle Infections", "infection, equine strongyle", "Strongyle Infection, Equine", "Infection, Equine Strongyle", "strongyle infections, equine", "infections, equine strongyle", "Strongyle Infections, Equine", "Infections, Equine Strongyle", "Infection by Strongylus equinus", "Infection by Strongylus equinus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "strongyle infections, equine", "shortest_name_length": 19}
{"curie": "MONDO:0011713", "names": ["FAMMMPC", "FAMMMPC Syndrome", "melanoma-pancreatic cancer syndrome", "Melanoma-Pancreatic Cancer Syndrome", "MELANOMA-PANCREATIC CANCER SYNDROME", "Familial Atypical Multiple Mole Melanoma-Pancreatic Carcinoma Syndrome", "familial atypical multiple Mole melanoma-pancreatic carcinoma syndrome", "FAMILIAL ATYPICAL MULTIPLE MOLE MELANOMA-PANCREATIC CARCINOMA SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melanoma-pancreatic cancer syndrome", "shortest_name_length": 7}
{"curie": "MONDO:0002077", "names": ["low implantation of placenta", "Placenta previa without hemorrhage", "PLACENTA PREVIA WITHOUT HEMORRHAGE", "placenta previa without hemorrhage", "placenta; previa, without hemorrhage", "Placenta praevia without haemorrhage", "Placenta previa without hemorrhage (disorder)", "pregnancy; placenta, previa without hemorrhage", "placenta previa without hemorrhage (diagnosis)", "Placenta previa specified as without hemorrhage", "Low implantation of placenta without hemorrhage", "Placenta praevia specified as without hemorrhage", "Low implantation of placenta without haemorrhage", "Placenta praevia specified as without haemorrhage", "Placenta previa found during pregnancy without hemorrhage", "Placenta praevia found during pregnancy without haemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "low implantation of placenta", "shortest_name_length": 28}
{"curie": "UMLS:C4288594", "names": ["Bartholin Gland Hyperplasia", "Bartholin Gland Nodular Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bartholin Gland Hyperplasia", "shortest_name_length": 27}
{"curie": "UMLS:C5419775", "names": ["Jejunal Neuroendocrine Tumor G3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jejunal Neuroendocrine Tumor G3", "shortest_name_length": 31}
{"curie": "UMLS:C4745056", "names": ["Locally Advanced Basal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Basal Cell Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0044644", "names": ["congenital scrotal absence", "congenital scrotal agenesis", "congenital absence of the scrotum", "congenital agenesis of the scrotum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital agenesis of the scrotum", "shortest_name_length": 26}
{"curie": "MONDO:0032566", "names": ["SQSD", "squalene synthase deficiency", "SQUALENE SYNTHASE DEFICIENCY", "neurodevelopmental disorder with low cholesterol and abnormal urine organic acids", "NEURODEVELOPMENTAL DISORDER WITH LOW CHOLESTEROL AND ABNORMAL URINE ORGANIC ACIDS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "squalene synthase deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0003765", "names": ["Adult Meningeal Melanoma", "adult meningeal melanoma", "Adult Leptomeningeal Melanoma", "adult leptomeningeal melanoma", "melanoma of adult leptomeninges", "melanoma of adult Leptomeninges", "Melanoma of Adult Leptomeninges", "Melanoma of the Adult Leptomeninges", "melanoma of the adult leptomeninges"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult leptomeningeal melanoma", "shortest_name_length": 24}
{"curie": "MONDO:0001118", "names": ["fever; Australian", "Australian; fever", "Australian; Q fever", "Q fever; Australian", "FEVER, AUSTRALIAN Q", "QUEENSLAND TICK TYPHUS", "Queensland Tick Typhus", "Queensland tick typhus", "Australian tick typhus", "Tick Typhus, Queensland", "Typhus, Queensland Tick", "North Queensland tick typhus", "Rickettsia australis infection", "Rickettsia australis Infection", "Rickettsia australis Infections", "Infection, Rickettsia australis", "Infections, Rickettsia australis", "Queensland tick typhus (disorder)", "Queensland tick typhus (diagnosis)", "Rickettsia australis spotted fever", "spotted fever; Rickettsia australis", "rickettsiosis; Rickettsia australis", "Rickettsia; australis, spotted fever", "Tick typhus due to Rickettsia australis", "Spotted fever due to Rickettsia australis", "australis; Rickettsia australis, spotted fever"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Queensland tick typhus", "shortest_name_length": 17}
{"curie": "MONDO:0012380", "names": ["DFNA53", "autosomal dominant deafness 53", "Deafness, Autosomal Dominant 53", "DEAFNESS, AUTOSOMAL DOMINANT 53", "deafness, autosomal dominant 53", "DEAFNESS, AUTOSOMAL DOMINANT 53 (disorder)", "autosomal dominant nonsyndromic deafness 53", "autosomal dominant nonsyndromic hearing loss 53", "autosomal dominant nonsyndromic deafness type 53", "deafness, autosomal dominant nonsyndromic sensorineural 53"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 53", "shortest_name_length": 6}
{"curie": "MONDO:0009301", "names": ["SRXY7", "GDXYM", "46XY sex reversal 7", "46,XY SEX reversal 7", "46,XY SEX REVERSAL 7", "46,XY sex reversal 7", "46,XY Sex reversal type 7", "GONADAL DYSGENESIS, XY, MALE-LIMITED", "gonadal dysgenesis, XY, male limited", "gonadal dysgenesis, XY, Male-limited", "Gonadal Dysgenesis, XY, Male Limited", "46,XY sex reversal, partial or complete, DHH-related", "46,XY Sex reversal, partial or complete, Dhh-related", "46,XY SEX REVERSAL, PARTIAL OR COMPLETE, DHH-RELATED", "46,XY Gonadal Dysgenesis, Complete or Partial, DHH-Related", "46,XY gonadal dysgenesis, partial or complete, Dhh-related", "46,XY gonadal dysgenesis, partial or complete, DHH-related", "46,XY GONADAL DYSGENESIS, PARTIAL OR COMPLETE, DHH-RELATED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XY sex reversal 7", "shortest_name_length": 5}
{"curie": "MONDO:0017534", "names": ["postaxial polydactyly type B, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postaxial polydactyly type B, bilateral", "shortest_name_length": 39}
{"curie": "MONDO:0100026", "names": ["myoclonic encephalopathy in non-progressive disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myoclonic encephalopathy in non-progressive disorder", "shortest_name_length": 52}
{"curie": "UMLS:C3272309", "names": ["Coronary Venous Dissection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Coronary Venous Dissection", "shortest_name_length": 26}
{"curie": "UMLS:C1332228", "names": ["Alcohol-Related Hepatocellular Cancer", "Liver Cancer Secondary to Alcohol Use", "Alcohol-Related Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alcohol-Related Hepatocellular Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0012874", "names": ["DSAP4", "POROK6", "POROKERATOSIS 6, MULTIPLE TYPES", "porokeratosis 6, multiple types", "porokeratosis 6, disseminated superficial", "POROKERATOSIS 6, DISSEMINATED SUPERFICIAL", "porokeratosis, disseminated superficial actinic, 4", "POROKERATOSIS, DISSEMINATED SUPERFICIAL ACTINIC, 4", "Porokeratosis, Disseminated Superficial Actinic, 4", "porokeratosis 6, disseminated superficial actinic type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "porokeratosis 6, disseminated superficial actinic type", "shortest_name_length": 5}
{"curie": "UMLS:C0333878", "names": ["Moderate Columnar Cell Atypia", "Moderate columnar cell atypia", "Moderate columnar cell atypia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Moderate columnar cell atypia", "shortest_name_length": 29}
{"curie": "UMLS:C0518443", "names": ["Abrasion", "abrasion skin", "Abrasion;skin", "skin abrasion", "Skin Abrasion", "skin abrasions", "Skin abrasions", "Abrasion of skin", "Abrasion and/or friction burn of skin", "Abrasion and/or friction burn of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin abrasion", "shortest_name_length": 8}
{"curie": "MONDO:0018548", "names": ["acute poisoning by drugs with membrane-stabilizing effect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute poisoning by drugs with membrane-stabilizing effect", "shortest_name_length": 57}
{"curie": "MONDO:0004223", "names": ["Ear polyp", "Ear Polyp", "polyp ear", "ear polyp", "ear polyps", "Otic polyp", "Aural polyp", "aural polyp", "Aural Polyp", "Polyp of Ear", "aural polyps", "Polyp of ear", "Polyp(s);ear(s)", "middle ear polyp", "Middle Ear Polyp", "Polyp of the Ear", "middle Ear polyp", "middle ear; polyp", "polyp; middle ear", "polyp - middle ear", "Polyp of middle ear", "Polyp of Middle Ear", "polyp of middle ear", "Polyp of the Middle Ear", "polyp of the middle ear", "Aural polyp of middle ear", "middle ear polyp (___ mm)", "Polyp of middle ear (disorder)", "polyp of middle ear (diagnosis)", "polyp of middle ear (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyp of middle ear", "shortest_name_length": 9}
{"curie": "UMLS:C0280298", "names": ["Anterior Tongue SCC", "Anterior Tongue Squamous Cell Carcinoma", "Squamous Cell Carcinoma of Anterior Tongue", "Squamous Cell Carcinoma of the Anterior Tongue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anterior Tongue Squamous Cell Carcinoma", "shortest_name_length": 19}
{"curie": "MONDO:0021474", "names": ["benign Ear tumor", "Benign Ear Tumor", "Benign Ear Neoplasm", "Neoplasm benign;ear", "Benign Tumor of Ear", "benign Ear neoplasm", "Benign ear neoplasm", "benign tumor of Ear", "ear benign neoplasm", "Aural neoplasms benign", "benign neoplasm of ear", "Benign Neoplasm of Ear", "Benign neoplasm of ear", "Benign Tumor of the Ear", "Aural Neoplasms, Benign", "benign tumor of the Ear", "aural neoplasms, benign", "benign neoplasm of the Ear", "benign neoplasm of the ear", "Benign Neoplasm of the Ear", "Benign neoplasm of ear (disorder)", "benign neoplasm of ear (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of ear", "shortest_name_length": 16}
{"curie": "MONDO:0007223", "names": ["BDE", "BDE1", "Brachydactyly type E", "Type E brachydactyly", "Brachydactyly, Type E", "brachydactyly type E1", "BRACHYDACTYLY, TYPE E", "brachydactyly, type E", "Brachydactyly, type E", "brachydactyly, type E1", "BRACHYDACTYLY, TYPE E1", "HOXD13 brachydactyly type E", "brachydactyly type E caused by mutation in HOXD13"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly type E1", "shortest_name_length": 3}
{"curie": "UMLS:C4727105", "names": ["Metastatic Breast Cancer in the Spine", "Breast Carcinoma Metastatic in the Spine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Carcinoma Metastatic in the Spine", "shortest_name_length": 37}
{"curie": "MONDO:0021029", "names": ["genetic sebaceous gland anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genetic sebaceous gland anomaly", "shortest_name_length": 31}
{"curie": "UMLS:C1706733", "names": ["Advanced Favorable Non-Hodgkin Lymphoma", "Advanced Favorable Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Favorable Non-Hodgkin Lymphoma", "shortest_name_length": 39}
{"curie": "MONDO:0009012", "names": ["froster-Iskenius-Waterson syndrome", "froster-Iskenius-Waterson-Hall syndrome", "malignant hyperthermia arthrogryposis torticollis", "multiple pterygium-malignant hyperthermia syndrome", "malignant hyperthermia - arthrogryposis - torticollis", "malignant hyperthermia-arthrogryposis-torticollis syndrome", "contractures, congenital, torticollis, and malignant hyperthermia", "Contractures, Congenital, Torticollis, and Malignant Hyperthermia", "CONTRACTURES, CONGENITAL, TORTICOLLIS, AND MALIGNANT HYPERTHERMIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple pterygium-malignant hyperthermia syndrome", "shortest_name_length": 34}
{"curie": "MONDO:0006411", "names": ["SNUC", "Sinonasal Anaplastic Carcinoma", "Sinonasal anaplastic carcinoma", "undifferentiated Sinonasal cancer", "Undifferentiated Sinonasal Cancer", "sinonasal undifferentiated carcinoma", "Sinonasal Undifferentiated Carcinoma", "Sinonasal undifferentiated carcinoma", "Undifferentiated carcinoma of nasal sinus", "SNUC - sinonasal undifferentiated carcinoma", "Undifferentiated carcinoma of nasal sinus (disorder)", "Undifferentiated carcinoma of nasal sinus (diagnosis)", "nasal sinus neoplasm malignant carcinoma undifferentiated", "highly aggressive undifferentiated carcinoma of the nasal cavity and paranasal sinuses"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sinonasal undifferentiated carcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0015726", "names": ["Trisomy 14qter", "trisomy 14qter", "distal trisomy 14q", "Distal trisomy 14q", "Duplication 14qter", "distal duplication 14q", "Distal duplication 14q", "distal trisomy type 14q", "Telomeric duplication 14q", "telomeric duplication 14q", "Chromosome 14q, terminal duplication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal trisomy 14q", "shortest_name_length": 14}
{"curie": "DOID:14275", "names": ["atrophy vulva", "vulvar atrophy", "vulva; atrophy", "Atrophic vulva", "atrophy; vulva", "atrophic vulva", "Vulval atrophic", "atrophied vulva", "atrophy of vulva", "Atrophy of vulva", "Atrophic vulvitis", "Atrophic vulva (disorder)", "atrophy of vulva (diagnosis)", "vulvar atrophy (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrophic vulva", "shortest_name_length": 13}
{"curie": "UMLS:C5417721", "names": ["SGAT", "Salivary Gland Anlage Tumor", "Congenital Salivary Gland Anlage Tumor", "Nasopharyngeal Salivary Gland Anlage Tumor", "Nasopharyngeal Congenital Pleomorphic Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasopharyngeal Salivary Gland Anlage Tumor", "shortest_name_length": 4}
{"curie": "UMLS:C4725848", "names": ["Unresectable Adrenal Cortex Carcinoma", "Unresectable Adrenal Cortical Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Adrenal Cortical Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0100503", "names": ["DPH5-related diphthamide-deficiency syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DPH5-related diphthamide-deficiency syndrome", "shortest_name_length": 44}
{"curie": "MONDO:0004012", "names": ["Adult Botryoid Sarcoma", "adult botryoid sarcoma", "adult botryoid rhabdomyosarcoma", "botryoid rhabdomyosarcoma of adults", "adult botryoid-type embryonal rhabdomyosarcoma", "Adult Botryoid-Type Embryonal Rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult botryoid rhabdomyosarcoma", "shortest_name_length": 22}
{"curie": "MONDO:0002858", "names": ["ovary rhabdomyosarcoma", "Ovarian Rhabdomyosarcoma", "ovarian rhabdomyosarcoma", "Rhabdomyosarcoma of Ovary", "rhabdomyosarcoma of ovary", "Rhabdomyosarcoma of the Ovary", "rhabdomyosarcoma of the ovary", "ovary rhabdomyosarcoma (disease)", "rhabdomyosarcoma (disease) of ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovary rhabdomyosarcoma", "shortest_name_length": 22}
{"curie": "MONDO:0013603", "names": ["MYP20", "myopia 20, autosomal dominant", "MYOPIA 20, AUTOSOMAL DOMINANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopia 20, autosomal dominant", "shortest_name_length": 5}
{"curie": "MONDO:0010401", "names": ["EDMD6", "XMPMA", "Emery-Dreifuss Muscular Dystrophy 6", "EMERY-DREIFUSS MUSCULAR DYSTROPHY 6", "Emery Dreifuss Muscular Dystrophy 6", "Ehlers-Danlos syndrome, classic-like, 1", "X-linked Emery-Dreifuss muscular dystrophy 6", "Emery-Dreifuss muscular dystrophy 6, X-linked", "Emery-Dreifuss Muscular Dystrophy 6, X-Linked", "EMERY-DREIFUSS MUSCULAR DYSTROPHY 6, X-LINKED", "Emery Dreifuss Muscular Dystrophy 6, X Linked", "X-linked myopathy with postural muscle atrophy", "Myopathy, X-Linked, With Postural Muscle Atrophy", "MYOPATHY, X-LINKED, WITH POSTURAL MUSCLE ATROPHY", "myopathy, X-linked, with postural muscle atrophy", "XMPMA - X-linked myopathy with postural muscle atrophy", "X-linked myopathy with postural muscle atrophy (disorder)", "MYOPATHY, X-LINKED, WITH POSTURAL MUSCLE ATROPHY (disorder)", "myopathy, X-linked, with postural muscle atrophy, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked myopathy with postural muscle atrophy", "shortest_name_length": 5}
{"curie": "UMLS:C4288243", "names": ["Borderline Broad Ligament Serous Tumor", "Serous Borderline Broad Ligament Tumor/Atypical Proliferative Serous Broad Ligament Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Broad Ligament Serous Tumor", "shortest_name_length": 38}
{"curie": "MONDO:0013324", "names": ["CATLPH", "choanal atresia and lymphedema", "CHOANAL ATRESIA AND LYMPHEDEMA", "Lymphedema-posterior choanal atresia syndrome", "lymphedema-posterior choanal atresia syndrome", "Lymphedema, posterior choanal atresia syndrome", "Lymphoedema, posterior choanal atresia syndrome", "Lymphedema, posterior choanal atresia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphedema-posterior choanal atresia syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C5235849", "names": ["Unresectable Metastatic PitNET", "Unresectable Pituitary Gland Carcinoma", "Metastatic Unresectable Pituitary Neuroendocrine Tumor", "Unresectable Metastatic Pituitary Neuroendocrine Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Unresectable Pituitary Neuroendocrine Tumor", "shortest_name_length": 30}
{"curie": "MONDO:0006287", "names": ["bone giant cell sarcoma", "Malignant osteoclastoma", "Giant Cell Bone Sarcoma", "giant cell bone sarcoma", "OSTEOCLASTOMA, MALIGNANT", "Osteoclastoma, malignant", "OSTEOCLASTOMA, malignant", "giant cell sarcoma of bone", "Giant Cell Sarcoma of Bone", "Giant cell sarcoma of bone", "giant cell sarcoma of the bone", "Giant Cell Sarcoma of the Bone", "Giant cell sarcoma of the bone", "Bone giant cell tumor malignant", "Bone giant cell tumour malignant", "Dedifferentiated giant cell tumor", "Dedifferentiated Giant Cell Tumor", "Malignant Giant Cell Tumor of Bone", "malignant giant cell tumor of bone", "Malignant giant cell tumor of bone", "giant cell tumor of bone, malignant", "Malignant giant cell tumour of bone", "Giant cell tumor of bone, malignant", "Giant cell tumour of bone, malignant", "giant cell sarcoma of bone (diagnosis)", "malignancy in giant cell tumor of bone", "Malignancy in Giant Cell Tumor of Bone", "malignancy in giant cell tumor of the bone", "Malignancy in Giant Cell Tumor of the Bone", "giant cell tumor of bone, malignant (morphologic abnormality)", "Giant cell tumor of bone, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignancy in giant cell tumor of bone", "shortest_name_length": 23}
{"curie": "UMLS:C1868846", "names": ["Injection site macule"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site macule", "shortest_name_length": 21}
{"curie": "UMLS:C0279779", "names": ["hairy cell leukemia, progressive post-splenectomy", "Progressive Hairy Cell Leukemia Initial Treatment", "Progressive Hairy Cell Leukemia, Initial Treatment", "leukemia, progressive hairy cell, post-splenectomy", "progressive hairy cell leukemia, initial treatment"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Progressive Hairy Cell Leukemia Initial Treatment", "shortest_name_length": 49}
{"curie": "UMLS:C1336118", "names": ["Stage IA Lung Cancer", "Stage IA Lung Carcinoma", "Stage IA Carcinoma of Lung", "Stage IA Lung Cancer AJCC v7", "Stage IA Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Lung Cancer AJCC v7", "shortest_name_length": 20}
{"curie": "UMLS:C0263465", "names": ["Skin xerosis", "skin; xerosis", "xerosis cutis", "Xerosis cutis", "xerosis; skin", "cutis; xerosis", "xerosis; cutis", "asteatosis cutis", "Asteatosis cutis", "xerosis cutis (diagnosis)", "Asteatosis cutis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Asteatosis cutis", "shortest_name_length": 12}
{"curie": "MONDO:0015133", "names": ["quantitative and/or qualitative congenital phagocyte defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "quantitative and/or qualitative congenital phagocyte defect", "shortest_name_length": 59}
{"curie": "UMLS:C0859872", "names": ["Corrosive Injury", "Corrosive injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Corrosive injury", "shortest_name_length": 16}
{"curie": "MONDO:0006766", "names": ["gait apraxia", "Apraxic gait", "Gait Apraxia", "apraxic gait", "Gait apraxia", "Gait Apraxias", "Apraxia, Gait", "Gait Dyspraxia", "Apraxias, Gait", "Apraxia of gait", "apraxia of gait", "Apraxia of Gait", "Gait Dyspraxias", "Dyspraxia of Gait", "Bruns Gait Apraxia", "Bruns Apraxia, Gait", "Bruns' Gait Apraxia", "Bruns' Gait Apraxias", "Apraxia, Bruns' Gait", "Bruns' Apraxia, Gait", "Gait Apraxia, Bruns'", "Apraxias, Bruns' Gait", "Bruns apraxia of gait", "Gait Apraxias, Bruns'", "Bruns' apraxia of gait", "Gait apraxia (finding)", "Bruns' Apraxia of Gait", "apraxic gait (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gait apraxia", "shortest_name_length": 12}
{"curie": "MONDO:0006957", "names": ["Root caries", "caries root", "root caries", "Root Caries", "Caries, Root", "caries roots", "Cementum caries", "cementum caries", "caries; cementum", "cementum; caries", "caries of cementum", "Caries of cementum", "Root surface caries", "Root caries (disorder)", "cementum dental caries", "caries of root surface", "Root caries (diagnosis)", "dental caries of cementum", "Cementum caries (disorder)", "Dental caries of root surface", "dental caries of root surface", "caries of cementum (diagnosis)", "caries of root surface (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "root caries", "shortest_name_length": 11}
{"curie": "MONDO:0022113", "names": ["CCCA", "Hot comb alopecia", "hot comb alopecia", "central centrifugal alopecia", "central centrifugal cicatricial alopecia", "CENTRAL CENTRIFUGAL CICATRICIAL ALOPECIA", "Central centrifugal cicatricial alopecia", "Central centrifugal cicatricial alopecia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central centrifugal cicatricial alopecia", "shortest_name_length": 4}
{"curie": "UMLS:C4521792", "names": ["IIIC", "Stage IIIC Gastric (Stomach) Cancer", "Pathologic Stage IIIC Gastric Cancer AJCC v8", "Pathologic Stage IIIC Gastric Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IIIC Gastric Cancer AJCC v8", "shortest_name_length": 4}
{"curie": "UMLS:C0572583", "names": ["Antimetabolite overdose", "Antimetabolite overdose (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Antimetabolite overdose", "shortest_name_length": 23}
{"curie": "MONDO:0005321", "names": ["FCED", "FECD", "Fuchs Atrophy", "dystrophy fuch", "dystrophy fuchs", "Atrophy, Fuchs'", "Fuchs Dystrophy", "Fuchs; dystrophy", "fuchs' dystrophy", "Fuchs' dystrophy", "dystrophy; Fuchs", "corneal dystrophy fuchs", "Fuchs corneal dystrophy", "Fuchs Corneal Dystrophy", "Fuchs' corneal dystrophy", "fuchs' corneal dystrophy", "corneal dystrophies fuchs", "Fuch Endothelial Dystrophy", "fuch endothelial dystrophy", "Fuchs Endothelial Dystrophy", "Fuchs endothelial dystrophy", "fuchs endothelial dystrophy", "fuch's endothelial dystrophy", "Fuch's Endothelial Dystrophy", "fuchs' endothelial dystrophy", "Fuch's endothelial dystrophy", "Fuchs' Endothelial Dystrophy", "Fuchs' endothelial dystrophy", "Endothelial Dystrophy, Fuch's", "Endothelial Dystrophy, Fuchs'", "Dystrophy, Fuch's Endothelial", "Dystrophy, Fuchs' Endothelial", "dystrophia epithelialis corneae", "Endoepithelial corneal dystrophy", "Fuchs Endothelial Corneal Dystrophy", "Fuchs' corneal dystrophy (disorder)", "Fuchs endothelial corneal dystrophy", "corneal dystrophy, Fuchs endothelial", "Fuch's endothelial corneal dystrophy", "Fuchs' endothelial corneal dystrophy", "corneal dystrophy endothelial Fuchs'", "obsolete_Fuchs' endothelial dystrophy", "Late hereditary endothelial dystrophy", "late hereditary endothelial dystrophy", "Fuchs' endothelial corneal dystrophy (diagnosis)", "Fuchs endothelial corneal dystrophy (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fuchs' endothelial dystrophy", "shortest_name_length": 4}
{"curie": "MONDO:0011299", "names": ["HLN1", "HDL1", "Huntington Disease-Like 1", "Huntington disease-like 1", "HUNTINGTON DISEASE-LIKE 1", "Huntington's disease-like 1", "Huntington disease-like type 1", "HDL1 - Huntington disease-like 1", "Huntington disease-like 1 (disorder)", "PRNP neurodegenerative disease with chorea", "Huntington-like neurodegenerative disorder 1", "Huntington-Like Neurodegenerative Disorder 1", "HUNTINGTON-LIKE NEURODEGENERATIVE DISORDER 1", "autosomal dominant Huntington-like neurodegenerative disorder", "Early-onset prion disease with prominent psychiatric features", "early-onset prion disease with prominent psychiatric features", "Huntington-Like Neurodegenerative Disorder, Autosomal Dominant", "Huntington-like neurodegenerative disorder, autosomal dominant", "HUNTINGTON-LIKE NEURODEGENERATIVE DISORDER, AUTOSOMAL DOMINANT", "Prion Disease, Early-Onset, With Prominent Psychiatric Features", "prion disease, early-onset, with prominent psychiatric features", "PRION DISEASE, EARLY-ONSET, WITH PROMINENT PSYCHIATRIC FEATURES", "neurodegenerative disease with chorea caused by mutation in PRNP"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Huntington disease-like 1", "shortest_name_length": 4}
{"curie": "UMLS:C4289818", "names": ["Cervical Leiomyoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Leiomyoma", "shortest_name_length": 18}
{"curie": "MONDO:0009220", "names": ["steatosis of liver", "Visceral steatosis", "visceral steatosis", "STEATOSIS OF LIVER", "White liver disease", "WHITE LIVER DISEASE", "Visceral Steatosis, Congenital", "fatty metamorphosis of viscera", "FATTY METAMORPHOSIS OF VISCERA", "visceral steatosis, congenital", "VISCERAL STEATOSIS, CONGENITAL", "Fatty metamorphosis of viscera", "Fatty Liver Disease, Congenital", "FATTY LIVER DISEASE, CONGENITAL", "fatty liver disease, congenital", "fatal neonatal hepatic steatosis", "Fatal neonatal hepatic steatosis", "Fatty metamorphosis of viscera (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "visceral steatosis, congenital", "shortest_name_length": 18}
{"curie": "UMLS:C4683150", "names": ["Stage IIB Posterior Uveal Melanoma AJCC v8", "Stage IIB Choroidal and Ciliary Body Melanoma", "Stage IIB Choroidal and Ciliary Body Melanoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Choroidal and Ciliary Body Melanoma AJCC v8", "shortest_name_length": 42}
{"curie": "MONDO:0020848", "names": ["OPTA3", "OSTEOPETROSIS, AUTOSOMAL DOMINANT 3", "OSTEOPETROSIS, autosomal dominant 3", "osteopetrosis, autosomal dominant 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteopetrosis, autosomal dominant 3", "shortest_name_length": 5}
{"curie": "MONDO:0016870", "names": ["partial monosomy of chromosome 5", "partial deletion of chromosome 5", "partial deletion of chromosome type 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of chromosome 5", "shortest_name_length": 32}
{"curie": "UMLS:C4727843", "names": ["Recurrent Submandibular Gland Carcinoma ex Pleomorphic Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Submandibular Gland Carcinoma ex Pleomorphic Adenoma", "shortest_name_length": 62}
{"curie": "UMLS:C0036903", "names": ["Sexual aversion", "sexual aversion", "sexual; aversion", "aversion; sexual", "Sexual aversion disorder", "sexual aversion disorder", "Sexual Aversion Disorder", "sexual aversion disorders", "Sexual Aversion Disorders", "sexual; disorder, aversion", "Disorders, Sexual Aversion", "disorder; sexual, aversion", "Aversion Disorders, Sexual", "Sexual aversion disorder (disorder)", "sexual aversion disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sexual Aversion Disorder", "shortest_name_length": 15}
{"curie": "UMLS:C4744371", "names": ["Intrasellar Meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intrasellar Meningioma", "shortest_name_length": 22}
{"curie": "UMLS:C1512255", "names": ["High Grade Endometrial Endometrioid Carcinoma", "High-Grade Endometrial Endometrioid Carcinoma", "Grade 3 Endometrial Endometrioid Adenocarcinoma", "High-Grade Endometrial Endometrioid Adenocarcinoma", "High Grade Endometrial Endometrioid Adenocarcinoma", "FIGO Grade 3 Endometrial Endometrioid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Endometrial Endometrioid Adenocarcinoma", "shortest_name_length": 45}
{"curie": "MONDO:0033262", "names": ["NPHS15", "nephrotic syndrome 15", "nephrotic syndrome type 15", "nephrotic syndrome, type 15", "NEPHROTIC SYNDROME, TYPE 15"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrotic syndrome 15", "shortest_name_length": 6}
{"curie": "MONDO:0011005", "names": ["trisomy 18-like syndrome", "TRISOMY 18-LIKE SYNDROME", "Trisomy 18-Like Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trisomy 18-like syndrome", "shortest_name_length": 24}
{"curie": "MONDO:0035401", "names": ["isolated anencephaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated anencephaly", "shortest_name_length": 20}
{"curie": "MONDO:0019172", "names": ["anirida", "aniridia", "Aniridia", "ANIRIDIA", "Irideremia", "irideremia", "Absent Iris", "Irideraemia", "Absent iris", "iris; absent", "absence; iris", "agenesis; iris", "iris; agenesis", "Absence of iris", "Aplasia of iris", "aplasia of iris", "Agenesis of iris", "Congenital Aniridia", "congenital aniridia", "Congenital aniridia", "aniridia (diagnosis)", "Congenital absence of iris", "aniridia (physical finding)", "Congenital aniridia (disorder)", "congenital aniridia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aniridia", "shortest_name_length": 7}
{"curie": "UMLS:C3160814", "names": ["cannabis use", "Cannabis use", "cannabis use (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cannabis use", "shortest_name_length": 12}
{"curie": "MONDO:0012929", "names": ["MYPCN", "congenital myopathy 12", "Compton-North congenital myopathy", "myopathy, congenital, Compton-NORTH", "MYOPATHY, CONGENITAL, COMPTON-NORTH", "Myopathy, Congenital, Compton-North", "congenital lethal myopathy, Compton-North type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Compton-North congenital myopathy", "shortest_name_length": 5}
{"curie": "UMLS:C5557351", "names": ["Benign Vulvar Phyllodes Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Vulvar Phyllodes Tumor", "shortest_name_length": 29}
{"curie": "UMLS:C4682585", "names": ["Stage IIIB Uterine Corpus Adenosarcoma", "Stage IIIB Uterine Corpus Adenosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Uterine Corpus Adenosarcoma AJCC v8", "shortest_name_length": 38}
{"curie": "MONDO:0012543", "names": ["OPA5", "optic atrophy 5", "OPTIC ATROPHY 5", "Optic atrophy 5", "OPTIC ATROPHY 5 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "optic atrophy 5", "shortest_name_length": 4}
{"curie": "MONDO:0002751", "names": ["blad", "Bladder Adenocarcinoma", "bladder adenocarcinoma", "Bladder adenocarcinoma", "adenocarcinoma, bladder", "Adenocarcinoma of bladder", "Adenocarcinoma of Bladder", "adenocarcinoma of bladder", "Bladder Adenocarcinoma NOS", "Bladder Adenocarcinoma, NOS", "Adenocarcinoma of the Bladder", "adenocarcinoma of the bladder", "BLADDER CANCER ADENOCARCINOMA", "Urinary Bladder Adenocarcinoma", "urinary bladder adenocarcinoma", "bladder cancer, adenocarcinoma", "Adenocarcinoma of Urinary Bladder", "adenocarcinoma of urinary bladder", "Adenocarcinoma of bladder (disorder)", "Adenocarcinoma of the Urinary Bladder", "adenocarcinoma of bladder (diagnosis)", "adenocarcinoma of the urinary bladder", "Bladder Adenocarcinoma, Not Otherwise Specified", "bladder adenocarcinoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder adenocarcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0014012", "names": ["CMT2Q", "DHTKD1 Charcot-Marie-Tooth disease", "Charcot-Marie-Tooth disease type 2Q", "Charcot-Marie-Tooth neuropathy type 2Q", "Charcot-Marie-Tooth neuropathy, type 2Q", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2Q", "Charcot-Marie-Tooth disease axonal type 2Q", "Charcot-Marie-Tooth disease, axonal, type 2Q", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Q", "autosomal dominant Charcot-Marie-Tooth disease type 2Q", "Autosomal dominant Charcot-Marie-Tooth disease type 2Q", "Charcot-Marie-Tooth disease caused by mutation in DHTKD1", "autosomal dominant axonal Charcot-Marie-Tooth disease type 2Q", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2Q", "Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2Q", "Autosomal dominant Charcot-Marie-Tooth disease type 2Q (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease axonal type 2Q", "shortest_name_length": 5}
{"curie": "UMLS:C1334055", "names": ["HPV-Related Malignancy", "Human Papilloma Virus-Related Malignancy", "Human Papillomavirus-Related Malignant Neoplasm", "Human Papilloma Virus-Related Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Human Papillomavirus-Related Malignant Neoplasm", "shortest_name_length": 22}
{"curie": "MONDO:0008233", "names": ["Chromaffinoma", "Pheochromocytoma", "PHEOCHROMOCYTOMA", "Chromaffin tumor", "pheochromocytoma", "Pheochromocytomas", "Chromaffin tumour", "Chromaffin tumors", "PHAEOCHROMOCYTOMA", "phaeochromocytoma", "Chromaffin tumours", "Pheochromocytoma NOS", "Pheochromocytoma, NOS", "Phaeochromocytoma NOS", "Phaeochromocytoma, NOS", "Chromaffin paraganglioma", "Pheochromocytoma syndrome", "pheochromocytoma, susceptibility to", "PHEOCHROMOCYTOMA, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pheochromocytoma", "shortest_name_length": 13}
{"curie": "UMLS:C4721660", "names": ["Stage IV Ovarian Teratoma", "Stage IV Ovarian Teratoma AJCC v7", "Stage IV Ovarian Teratoma AJCC v6", "Stage IV Ovarian Germ Cell Teratoma", "Ovarian Germ Cell Teratoma Stage IV", "Ovarian Germ Cell Teratoma, Stage IV", "Stage IV Ovarian Teratoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Ovarian Teratoma AJCC v6 and v7", "shortest_name_length": 25}
{"curie": "UMLS:C5420332", "names": ["Salivary Gland Lipoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Salivary Gland Lipoma", "shortest_name_length": 21}
{"curie": "MONDO:0012191", "names": ["COXPD1", "Hepatoencephalopathy due to COXPD1", "hepatoencephalopathy due to COXPD1", "early fatal progressive hepatoencephalopathy", "Hepatoencephalopathy, Early Fatal Progressive", "HEPATOENCEPHALOPATHY, EARLY FATAL PROGRESSIVE", "Hepatoencephalopathy, early fatal progressive", "Combined Oxidative Phosphorylation Deficiency 1", "combined oxidative phosphorylation deficiency 1", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 1", "GFM1 combined oxidative phosphorylation deficiency", "combined oxidative phosphorylation deficiency type 1", "combined oxidative phosphorylation deficiency caused by mutation in GFM1", "Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1", "hepatoencephalopathy due to combined oxidative phosphorylation defect type 1", "Hepatoencephalopathy due to COXPD1 (combined oxidative phosphorylation defect type 1)", "Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatoencephalopathy due to combined oxidative phosphorylation defect type 1", "shortest_name_length": 6}
{"curie": "UMLS:C0013589", "names": ["ectromelia", "ECTROMELIA", "Ectromelia", "Ectromelia, NOS", "Ectromelia (disorder)", "Ectromelia of unspecified limb", "Congenital Limb Reduction Deformity", "Congenital Limb Reduction Deformities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ectromelia", "shortest_name_length": 10}
{"curie": "UMLS:C5447726", "names": ["SOMATIC_MALIGNANCY_TYPE", "Somatic-Type Malignancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Somatic-Type Malignancy", "shortest_name_length": 23}
{"curie": "UMLS:C3897758", "names": ["Recurrent Astrocytic Tumor", "Recurrent Childhood Astrocytic Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Astrocytic Tumor", "shortest_name_length": 26}
{"curie": "MONDO:0012516", "names": ["MFDM", "MFDGA", "MFDM syndrome", "mandibulofacial dysostosis with microcephaly", "MANDIBULOFACIAL DYSOSTOSIS WITH MICROCEPHALY", "Mandibulofacial dysostosis with microcephaly", "Mandibulofacial dysostosis, Guion-Almeida type", "mandibulofacial dysostosis, Guion-Almeida type", "MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE", "mandibulofacial dysostosis-microcephaly syndrome", "Mandibulofacial dysostosis-microcephaly syndrome", "Mandibulofacial dysostosis with microcephaly (disorder)", "GROWTH AND MENTAL RETARDATION, MANDIBULOFACIAL DYSOSTOSIS, MICROCEPHALY, AND CLEFT PALATE", "Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate", "Growth and intellectual disability, mandibulofacial dysostosis, microcephaly, and cleft palate", "Growth delay - intellectual disability - mandibulofacial dysostosis - microcephaly - cleft palate", "Growth delay-intellectual disability-mandibulofacial dysostosis-microcephaly-cleft palate syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mandibulofacial dysostosis-microcephaly syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0027663", "names": ["Synchronous Neoplasm", "Synchronous Neoplasms", "Neoplasm, Synchronous", "synchronous neoplasms", "Neoplasms, Synchronous", "Multiple Primary Neoplasm", "multiple primary neoplasia", "Primary Neoplasm, Multiple", "Multiple Primary Neoplasms", "Neoplasm, Multiple Primary", "Primary Neoplasms, Multiple", "Neoplasms, Multiple Primary", "synchronous multiple primary neoplasm", "Synchronous Multiple Primary Neoplasms", "Multiple Primary Neoplasms, Synchronous", "Neoplasms, Synchronous Multiple Primary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplasms, Multiple Primary", "shortest_name_length": 20}
{"curie": "UMLS:C5446581", "names": ["Locally Advanced Distal Bile Duct Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Distal Bile Duct Carcinoma", "shortest_name_length": 43}
{"curie": "UMLS:C1334414", "names": ["Low Grade Dysplasia in Barrett Esophagus", "Low Grade Dysplasia in Barrett's Esophagus", "Barretts esophagus with low grade dysplasia", "Barrett's esophagus with low grade dysplasia", "Barretts oesophagus with low grade dysplasia", "Barretts esophagus with low grade dysplasia (disorder)", "Barrett's esophagus with low grade dysplasia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Barretts esophagus with low grade dysplasia", "shortest_name_length": 40}
{"curie": "MONDO:0020593", "names": ["Brooke tumor", "Brooke's tumor", "trichoblastoma", "Trichoblastoma", "Brooke's Tumor", "Brooke's tumour", "Trichoepithelioma", "trichoepithelioma", "trichoepitheliomas", "Trichoblastoma (disorder)", "Trichogenic Adnexal Tumor", "TRICHOEPITHELIOMA, BENIGN", "trichogenic adnexal tumor", "trichoepithelioma, benign", "trichogenic trichoblastoma", "Trichogenic Trichoblastoma", "Trichoepithelioma (disorder)", "trichoepithelioma (diagnosis)", "epithelioma adenoides cysticum", "Epithelioma adenoides cysticum", "Trichoblastoma (morphologic abnormality)", "Trichoepithelioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichoblastoma", "shortest_name_length": 12}
{"curie": "UMLS:C0751858", "names": ["Mercury Psychosis", "Psychosis, Mercury", "Mercurial Psychosis", "Psychosis, Mercurial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mercury Psychosis", "shortest_name_length": 17}
{"curie": "UMLS:C0275566", "names": ["Thoracic actinomycosis", "THORACIC ACTINOMYCOSIS", "pulmonary actinomycosis", "Pulmonary actinomycosis", "actinomycosis; pulmonary", "pulmonary; actinomycosis", "Actinomycotic pulmonary infection", "Pulmonary actinomycotic infection", "Pulmonary actinomycosis (disorder)", "pulmonary actinomycosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pulmonary actinomycosis", "shortest_name_length": 22}
{"curie": "MONDO:0032636", "names": ["MC1DN33", "nuclear type mitochondrial complex I deficiency 33", "mitochondrial complex 1 deficiency, nuclear type 33", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 33"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 33", "shortest_name_length": 7}
{"curie": "MONDO:0002706", "names": ["cervix endometriosis", "Endometriosis, cervix", "cervical Endometriosis", "cervical endometriosis", "Cervical Endometriosis", "Cervical endometriosis", "endometriosis of cervix", "Endometriosis of cervix", "Endometriosis of the cervix", "Endometriosis of cervix (disorder)", "endometriosis of cervix (diagnosis)", "uterine cervix endometriosis (disease)", "endometriosis (disease) of uterine cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervix endometriosis", "shortest_name_length": 20}
{"curie": "MONDO:0012010", "names": ["CHDS4", "Chds4", "CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 4", "coronary heart disease, susceptibility to, 4", "coronary heart disease, susceptibility to, type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coronary heart disease, susceptibility to, 4", "shortest_name_length": 5}
{"curie": "MONDO:0017190", "names": ["sporadic pheochromocytoma/secreting paraganglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sporadic pheochromocytoma/secreting paraganglioma", "shortest_name_length": 49}
{"curie": "UMLS:C1335662", "names": ["Radiation anemia", "Radiation Anemia", "Radiation anaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radiation anemia", "shortest_name_length": 16}
{"curie": "MONDO:0011846", "names": ["BN", "BULN", "BULN2", "BULN1", "BULIMIA NERVOSA, SUSCEPTIBILITY TO", "bulimia nervosa, susceptibility to", "susceptibility to bulimia nervosa 2", "bulimia nervosa, susceptibility to, 1", "bulimia nervosa, susceptibility to, 2", "BULIMIA NERVOSA, SUSCEPTIBILITY TO, 1", "anorexia nervosa, susceptibility to, 2", "bulimia nervosa, susceptibility to, type 2", "BULIMIA NERVOSA, SUSCEPTIBILITY TO, 1 (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bulimia nervosa, susceptibility to, 1", "shortest_name_length": 2}
{"curie": "MONDO:0003413", "names": ["Hair matrix tumor", "Hair Matrix Tumor", "hair matrix tumor", "hair matrix tumour", "Hair matrix tumour", "Hair Follicle Tumor", "hair follicle tumor", "Hair follicle tumor", "Hair Matrix Neoplasm", "hair matrix neoplasm", "Hair Matrix neoplasm", "Hair follicle tumour", "Hair follicle neoplasm", "Hair Follicle Neoplasm", "tumor of hair follicle", "hair follicle neoplasm", "neoplasm of hair follicle", "Neoplasm of Hair Follicle", "neoplasm of the hair follicle", "Neoplasm of the Hair Follicle", "hair follicle neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hair follicle neoplasm", "shortest_name_length": 17}
{"curie": "UMLS:C0751366", "names": ["Radiation Induced Cancer", "Radiation-Related Cancer", "radiation related cancer", "Radiation-Induced Cancer", "radiation induced cancer", "cancer induced radiation", "radiation-induced cancers", "Radiation-Induced Cancers", "Cancer, Radiation Induced", "Cancer, Radiation-Induced", "Cancers, Radiation-Induced", "radiation related neoplasm/cancer", "Radiation-Related Malignant Neoplasm", "Radiation-Induced Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radiation-Induced Cancer", "shortest_name_length": 24}
{"curie": "MONDO:0009362", "names": ["game-Friedman-Paradice syndrome", "game Friedman Paradice syndrome", "Game-Friedman-Paradice syndrome", "Game Friedman Paradice syndrome", "HYDROCEPHALUS WITH ASSOCIATED MALFORMATIONS", "hydrocephalus with associated malformations", "Hydrocephalus with associated malformations", "growth delay-hydrocephaly-lung hypoplasia syndrome", "Growth delay-hydrocephaly-lung hypoplasia syndrome", "Growth delay with hydrocephalus and lung hypoplasia syndrome", "Growth delay with hydrocephalus and lung hypoplasia syndrome (disorder)", "retarded growth, hydrocephalus, micrognathia, intestinal malrotation, omphalocele, short lower limbs and foot deformities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "growth delay-hydrocephaly-lung hypoplasia syndrome", "shortest_name_length": 31}
{"curie": "MONDO:0009085", "names": ["deafness vitiligo achalasia", "deafness-vitiligo-achalasia syndrome", "congenital deafness with vitiligo and achalasia", "Deafness, Congenital, with Vitiligo and Achalasia", "deafness, congenital, with vitiligo and achalasia", "DEAFNESS, CONGENITAL, WITH VITILIGO AND ACHALASIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness-vitiligo-achalasia syndrome", "shortest_name_length": 27}
{"curie": "MONDO:0014158", "names": ["NPHP16", "nephronophthisis 16", "NEPHRONOPHTHISIS 16", "nephronophthisis type 16", "infantile nephronophthisis", "ANKS6 nephronophthisis (disease)", "autosomal recessive infantile NPHP", "autosomal recessive infantile nephronophthisis", "nephronophthisis (disease) caused by mutation in ANKS6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephronophthisis 16", "shortest_name_length": 6}
{"curie": "MONDO:0032798", "names": ["IKSHD", "ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facies", "ICHTHYOTIC KERATODERMA, SPASTICITY, HYPOMYELINATION, AND DYSMORPHIC FACIAL FEATURES", "ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features", "shortest_name_length": 5}
{"curie": "MONDO:0001699", "names": ["tinea manus", "Tinea manus", "tinea manuum", "Tinea manuum", "Tinea of hand", "manuum; tinea", "Hand ringworm", "tinea; manuum", "ringworm; hand", "hand; ringworm", "manus dermatophytosis", "hand; dermatophytosis", "dermatophytosis; hand", "Tinea manus (disorder)", "Dermatophytosis of hand", "dermatophytosis of hand", "tinea manuum (diagnosis)", "dermatophytosis of manus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tinea manuum", "shortest_name_length": 11}
{"curie": "MONDO:0013788", "names": ["USH3B", "HARS Usher syndrome", "Usher syndrome type 3B", "Usher syndrome, type 3B", "Usher syndrome type IIIB", "USHER syndrome, type IIIB", "USHER SYNDROME, TYPE IIIB", "Usher syndrome caused by mutation in HARS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Usher syndrome type 3B", "shortest_name_length": 5}
{"curie": "UMLS:C4763839", "names": ["Metastatic Micropapillary Urothelial Carcinoma", "Metastatic Micropapillary Bladder Urothelial Carcinoma", "Metastatic Micropapillary Urothelial Carcinoma of the Bladder", "Metastatic Infiltrating Bladder Urothelial Carcinoma, Micropapillary Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Infiltrating Bladder Urothelial Carcinoma, Micropapillary Variant", "shortest_name_length": 46}
{"curie": "UMLS:C0549294", "names": ["Neutropenia aggravated", "NEUTROPENIA AGGRAVATED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neutropenia aggravated", "shortest_name_length": 22}
{"curie": "UMLS:C0011346", "names": ["Materia Alba", "Tooth deposit", "dental deposit", "DEPOSITS TOOTH", "Deposits tooth", "Dental Deposit", "teeth; deposit", "Dental Deposits", "Deposit, Dental", "Dental deposits", "Deposits, Dental", "Deposits on tooth", "deposition; teeth", "accretions; teeth", "Tooth deposit, NOS", "Accretion on tooth", "Accretion on teeth", "Deposition on teeth", "Accretions on teeth", "Accretions on tooth", "accretions on tooth", "Accretion on teeth, NOS", "Deposition on teeth, NOS", "Accretion on tooth (disorder)", "Accretion on teeth (disorder)", "Deposits [accretions] on teeth", "accretions on tooth (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dental Deposits", "shortest_name_length": 12}
{"curie": "UMLS:C5420156", "names": ["Nasopharyngeal Non-Neoplastic Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasopharyngeal Non-Neoplastic Disorder", "shortest_name_length": 38}
{"curie": "MONDO:0015777", "names": ["adult hypothyroidism", "rare adult hypothyroidism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult hypothyroidism", "shortest_name_length": 20}
{"curie": "MONDO:0035404", "names": ["mucinous cystadenoma of childhood", "Mucinous cystadenoma of ovary in childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucinous cystadenoma of childhood", "shortest_name_length": 33}
{"curie": "MONDO:0001875", "names": ["TENNIS ELBOW", "Tennis elbow", "Tennis Elbow", "tennis elbow", "hockey elbow", "tennis elbows", "epicondylitis", "Tennis Elbows", "EPICONDYLITIS", "Epicondylitis", "ELBOW, TENNIS", "Elbow, Tennis", "Epitrochleitis", "golfer's elbow", "archer's elbow", "shooter's elbow", "Epicondylitis NOS", "Epicondylitis, NOS", "andrel epicondylitis", "medial epicondylitis", "lateral epicondylitis", "Lateral Epicondylitis", "Lateral epicondylitis", "Tennis elbow syndrome", "radiohumeral bursitis", "radiohumeral; bursitis", "Epicondylitis, Lateral", "lateral; epicondylitis", "BURSITIS, RADIOHUMERAL", "epicondylitis; lateral", "bursitis; radiohumeral", "lateralis epicondylitis", "epicondylitis lateralis", "Lateral Epicondylitides", "Epicondylitis;lateralis", "Epicondylitis (disorder)", "Epicondylitides, Lateral", "epicondylitis (diagnosis)", "EPICONDYLITIS, RADIOHUMERAL", "lateral humeral epicondylitis", "Lateral Humeral Epicondylitis", "Epicondylitis, Lateral Humeral", "Lateral epicondylitis of elbow", "Humeral Epicondylitis, Lateral", "Lateral Humeral Epicondylitides", "Epicondylitis syndrome of elbow", "Epicondylitides, Lateral Humeral", "Humeral Epicondylitides, Lateral", "Lateral epicondylitis (disorder)", "lateral epicondylitis (diagnosis)", "Lateral Epicondylitis (Tennis Elbow)", "lateral epicondylitis (tennis elbow)", "ectepicondyle of humerus inflammation", "inflammation of ectepicondyle of humerus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epicondylitis", "shortest_name_length": 12}
{"curie": "MONDO:0016449", "names": ["mid-dermal elastolysis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mid-dermal elastolysis", "shortest_name_length": 22}
{"curie": "MONDO:0006309", "names": ["MSTAD", "Mucinous adenocarcinoma gastric", "mucinous gastric adenocarcinoma", "stomach mucinous adenocarcinoma", "Mucinous Stomach Adenocarcinoma", "Gastric Mucinous Adenocarcinoma", "mucinous stomach adenocarcinoma", "Mucinous Gastric Adenocarcinoma", "Mucinous (colloid) adenocarcinoma", "Mucinous (Colloid) adenocarcinoma", "Mucinous Adenocarcinoma of Stomach", "mucinous adenocarcinoma of stomach", "mucinous adenocarcinoma of the stomach", "Mucinous Adenocarcinoma of the Stomach", "mucinous adenocarcinoma of stomach (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucinous gastric adenocarcinoma", "shortest_name_length": 5}
{"curie": "UMLS:C3272524", "names": ["Small Intestinal High Grade B-Cell Lymphoma, Not Otherwise Specified", "Small Intestinal B-Cell Lymphoma, Unclassifiable, with Features Intermediate between Diffuse Large B-Cell Lymphoma and Burkitt Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Intestinal High Grade B-Cell Lymphoma, Not Otherwise Specified", "shortest_name_length": 68}
{"curie": "MONDO:0007409", "names": ["Tonoki Ohura Niikawa syndrome", "Tonoki-Ohura-Niikawa syndrome", "Cryptomicrotia-brachydactyly syndrome", "CRYPTOMICROTIA-brachydactyly syndrome", "Cryptomicrotia brachydactyly syndrome", "Cryptomicrotia-Brachydactyly Syndrome", "CRYPTOMICROTIA-BRACHYDACTYLY SYNDROME", "Cryptomicrotia brachydactyly syndrome (disorder)", "Cryptomicrotia brachydactyly syndrome excess fingertip arch", "Cryptomicrotia-brachydactyly-excess fingertip arch syndrome", "cryptomicrotia-brachydactyly-excess fingertip arch syndrome", "Cryptomicrotia, brachydactyly, excess fingertip arch syndrome", "bilateral cryptomicrotia, brachytelomesophalangy, hypoplastic toe nails, and excess fingertip arch"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cryptomicrotia-brachydactyly-excess fingertip arch syndrome", "shortest_name_length": 29}
{"curie": "MONDO:0100244", "names": ["PNH", "pnh", "Marchiafava-Micheli", "paroxysmal hemoglobinuria", "Paroxysmal Hemoglobinuria", "Paroxysmal hemoglobinuria", "paroxysmal haemoglobinuria", "Hemoglobinuria, Paroxysmal", "hemoglobinuria; paroxysmal", "paroxysmal; hemoglobinuria", "Marchiafava-Micheli disease", "Marchiafava Micheli disease", "Marchiafava-Micheli syndrome", "MARCHIAFAVA-MICHELI SYNDROME", "Marchiafava Micheli Syndrome", "marchiafava-micheli syndrome", "Marchiafava-Micheli Syndrome", "Syndrome, Marchiafava-Micheli", "Paroxysmal nocturnal hemoglobinuria", "PAROXYSMAL NOCTURNAL HEMOGLOBINURIA", "Nocturnal Paroxysmal Hemoglobinuria", "Nocturnal paroxysmal hemoglobinuria", "HEMOGLOBINURIA PAROXYSMAL NOCTURNAL", "Paroxysmal Nocturnal Hemoglobinuria", "paroxysmal nocturnal hemoglobinuria", "Paroxysmal Hemoglobinuria, Nocturnal", "Hemoglobinuria, Paroxysmal Nocturnal", "Paroxysmal nocturnal haemoglobinuria", "Hemoglobinuria, Nocturnal Paroxysmal", "HEMOGLOBINURIA, PAROXYSMAL, NOCTURNAL", "hemoglobinuria; paroxysmal, nocturnal", "paroxysmal; hemoglobinuria, nocturnal", "Paroxysmal nocturnal hemoglobinuria (PNH)", "PNH - Paroxysmal nocturnal hemoglobinuria", "paroxysmal nocturnal hemoglobinuria (PNH)", "PNH - Paroxysmal nocturnal haemoglobinuria", "acquired paroxysmal nocturnal hemoglobinuria", "inherited paroxysmal nocturnal hemoglobinuria", "Paroxysmal nocturnal hemoglobinuria (disorder)", "hereditary paroxysmal nocturnal hemoglobinuria", "paroxysmal nocturnal hemoglobinuria (diagnosis)", "Paroxysmal nocturnal hemoglobinuria [Marchiafava-Micheli]", "Paroxysmal nocturnal haemoglobinuria [Marchiafava-Micheli]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paroxysmal nocturnal hemoglobinuria", "shortest_name_length": 3}
{"curie": "MONDO:0013205", "names": ["FECD5", "Fcd3 locus", "FCD3 LOCUS", "Corneal Dystrophy, Fuchs Endothelial, 5", "corneal dystrophy, Fuchs endothelial, 5", "CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 5", "corneal dystrophy, fuchs endothelial, 5", "CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, LATE-ONSET", "corneal dystrophy, Fuchs endothelial, late-onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal dystrophy, fuchs endothelial, 5", "shortest_name_length": 5}
{"curie": "UMLS:C1332596", "names": ["Borderline Ovarian Seromucinous Tumor/Atypical Proliferative Ovarian Seromucinous Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Ovarian Seromucinous Tumor/Atypical Proliferative Ovarian Seromucinous Tumor", "shortest_name_length": 87}
{"curie": "MONDO:0001555", "names": ["Neonatal thyrotoxicosis", "neonatal thyrotoxicosis", "Neonatal Thyrotoxicosis", "thyrotoxicosis; neonatal", "neonatal; thyrotoxicosis", "infantile hyperthyroidism", "Infantile Hyperthyroidism", "Neonatal thyrotoxicosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal thyrotoxicosis", "shortest_name_length": 23}
{"curie": "UMLS:C1707300", "names": ["Heart Intramuscular Hemangioma", "Cardiac Intramuscular Hemangioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiac Intramuscular Hemangioma", "shortest_name_length": 30}
{"curie": "MONDO:0009670", "names": ["Lccs", "LCCS", "LCCS1", "Herva disease", "Lethal congenital contracture syndrome", "Lethal congenital contracture syndrome 1", "lethal congenital contracture syndrome 1", "LETHAL CONGENITAL CONTRACTURE SYNDROME 1", "Multiple contracture syndrome Finnish type", "GLE1 lethal congenital contracture syndrome", "MULTIPLE CONTRACTURE SYNDROME, FINNISH TYPE", "multiple contracture syndrome, Finnish type", "Multiple contracture syndrome, Finnish type", "lethal congenital contracture syndrome type 1", "Lethal congenital contracture syndrome type 1", "Lethal congenital contracture syndrome type 1 (disorder)", "lethal congenital contracture syndrome caused by mutation in GLE1", "Lethal autosomal recessive syndrome of multiple congenital contractures", "lethal autosomal recessive syndrome of multiple congenital contractures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal congenital contracture syndrome 1", "shortest_name_length": 4}
{"curie": "UMLS:C0028313", "names": ["Nonpsychotic Organic Brain Syndrome", "Organic Brain Syndrome, Nonpsychotic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Organic Brain Syndrome, Nonpsychotic", "shortest_name_length": 35}
{"curie": "UMLS:C0339961", "names": ["Fungal pneumonia", "fungal pneumonia", "PNEUMONIA FUNGAL", "Pneumonia fungal", "pneumonia fungal", "pneumonia; fungus", "fungal pneumonias", "fungus; pneumonia", "Pneumonia fungal NOS", "Pneumonia in mycoses", "pneumonia in mycoses", "Fungal pneumonia (disorder)", "fungal pneumonia (diagnosis)", "pneumonia in mycoses (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fungal pneumonia", "shortest_name_length": 16}
{"curie": "UMLS:C1290161", "names": ["Infected bursa", "Septic bursitis", "septic bursitis", "BURSITIS SEPTIC", "Bursitis infective", "infective bursitis", "bursitis infective", "Infectious bursitis", "infective; bursitis", "bursitis; infective", "Bursitis infective NOS", "Infected bursa (disorder)", "septic bursitis (diagnosis)", "infective bursitis (diagnosis)", "bursitis caused by bacterial infection", "Bursitis caused by bacterial infection", "Bursitis caused by bacterial infection (disorder)", "bursitis caused by bacterial infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bursitis caused by bacterial infection", "shortest_name_length": 14}
{"curie": "MONDO:0003450", "names": ["eccrine papillary adenoma", "Papillary eccrine adenoma", "Papillary Eccrine Adenoma", "Eccrine papillary adenoma", "Eccrine Papillary Adenoma", "papillary eccrine adenoma", "eccrine papillary adenoma of skin", "Eccrine papillary adenoma of skin", "Eccrine papillary adenoma morphology", "Eccrine papillary adenoma of skin (disorder)", "Eccrine papillary adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eccrine papillary adenoma", "shortest_name_length": 25}
{"curie": "MONDO:0018604", "names": ["FCCTX", "Familial colorectal cancer type X", "Familial colorectal cancer Type X", "Familial Colorectal Cancer Type X", "familial colorectal cancer type X", "FCCTX - familial colorectal cancer type X", "Familial colorectal cancer type X (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial colorectal cancer type X", "shortest_name_length": 5}
{"curie": "UMLS:C4053898", "names": ["Undifferentiated epithelioid sarcoma", "Undifferentiated Epithelioid Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Undifferentiated Epithelioid Sarcoma", "shortest_name_length": 36}
{"curie": "MONDO:0013756", "names": ["PHOAR2", "PDP, AUTOSOMAL RECESSIVE", "PDP, autosomal recessive", "pachydermoperiostosis, autosomal recessive", "PACHYDERMOPERIOSTOSIS, AUTOSOMAL RECESSIVE", "SLCO2A1 primary hypertrophic osteoarthropathy", "hypertrophic osteoarthropathy, primary, autosomal recessive 2", "hypertrophic osteoarthropathy, primary, autosomal recessive, 2", "HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 2", "hypertrophic osteoarthropathy, primary, autosomal recessive, type 2", "primary hypertrophic osteoarthropathy caused by mutation in SLCO2A1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophic osteoarthropathy, primary, autosomal recessive, 2", "shortest_name_length": 6}
{"curie": "MONDO:0002949", "names": ["basal cell carcinoma, morphea", "Basal cell carcinoma, morphea", "Morpheic basal cell carcinoma", "Basal cell carcinoma, morphoea", "Basal cell carcinoma, morpheic", "Basal cell carcinoma - morpheic", "Cicatrising basal cell carcinoma", "cicatricial basal-cell carcinoma", "Cicatricial basal-cell carcinoma", "Morpheaform Basal Cell Carcinoma", "morpheaform basal cell carcinoma", "Basal cell carcinoma - morphoeic", "Morpheaform basal cell carcinoma", "Morphea-Type Basal Cell Carcinoma", "morphea-type basal cell carcinoma", "Morphoeaform basal cell carcinoma", "Basal cell carcinoma, morphea type", "basal cell carcinoma sclerosing type", "Sclerosing Type Basal Cell Carcinoma", "Basal Cell Carcinoma Sclerosing Type", "sclerosing type basal cell carcinoma", "Basal cell carcinoma, sclerosing type", "Basal cell carcinoma - sclerosing type", "Morpheic basal cell carcinoma (disorder)", "Morpheic basal cell carcinoma (diagnosis)", "Morphea-Type (Sclerosing) Basal Cell Carcinoma", "Morphea-type (Sclerosing) Basal cell carcinoma", "Skin Sclerosing/Morphoeic Basal Cell Carcinoma", "morphea-type (sclerosing) basal cell carcinoma", "malignant neoplasm carcinoma basal cell morpheic", "Skin Morphea-Type (Sclerosing) Basal Cell Carcinoma", "skin morphea-type (sclerosing) basal cell carcinoma", "Basal cell carcinoma - morpheic (morphologic abnormality)", "Basal cell carcinoma - sclerosing type (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "morpheaform basal cell carcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0005984", "names": ["Foot tinea", "tinea; foot", "pedis tinea", "foot; tinea", "tinea pedis", "TINEA PEDIS", "Tinea Pedis", "Tinea pedis", "tinea; pedis", "athlete foot", "Athlete Foot", "pedis; tinea", "Foot ringworm", "foot ringworm", "Athletes Foot", "athletes foot", "Mycosis pedis", "foot; ringworm", "athlete's foot", "ringworm; foot", "athletes foots", "Athlete's Foot", "Athlete's foot", "ringworm of foot", "TP - Tinea pedis", "Ringworm of foot", "pes dermatophytosis", "foot; dermatophytosis", "dermatophytosis; foot", "Epidermophytosis pedis", "dermatophytosis of pes", "Tinea pedis (disorder)", "tinea pedis (diagnosis)", "Dermatophytosis of foot", "dermatophytosis of foot"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tinea pedis", "shortest_name_length": 10}
{"curie": "MONDO:0015411", "names": ["Cleft face", "cleft face", "face cleft", "Facial cleft", "Facial Cleft", "cleft facial", "facial cleft", "Facial clefts", "facial clefts", "Prosoposchisis", "prosoposchisis", "Cleft of the face", "craniofacial cleft", "Craniofacial cleft", "Tessier facial cleft", "Craniofacial cleft (disorder)", "Craniofacial cleft (diagnosis)", "congenital deformity of head craniofacial cleft"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "facial cleft", "shortest_name_length": 10}
{"curie": "UMLS:C5237064", "names": ["Resectable Liver and Intrahepatic Bile Duct Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Liver and Intrahepatic Bile Duct Carcinoma", "shortest_name_length": 53}
{"curie": "MONDO:0034217", "names": ["resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta", "shortest_name_length": 80}
{"curie": "UMLS:C4086902", "names": ["Third Trimester Antepartum Hemorrhage", "Antepartum Hemorrhage, Third Trimester"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Third Trimester Antepartum Hemorrhage", "shortest_name_length": 37}
{"curie": "MONDO:0016263", "names": ["body of uterus primitive neuroectodermal tumor", "primitive neuroectodermal tumor of body of uterus", "primitive neuroectodermal tumor of the corpus uteri", "peripheral neuroectodermal cancer of the corpus uteri", "malignant peripheral neuroectodermal tumor of the corpus uteri"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primitive neuroectodermal tumor of the corpus uteri", "shortest_name_length": 46}
{"curie": "UMLS:C0263266", "names": ["Dermatitis due to Alkalis", "Dermatitis due to alkalis", "Contact dermatitis due to alkali", "contact dermatitis due to alkalis", "Contact dermatitis caused by alkali", "contact dermatitis due to alkalis (diagnosis)", "Contact dermatitis caused by alkali (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Contact dermatitis due to alkali", "shortest_name_length": 25}
{"curie": "UMLS:C4288551", "names": ["Oropharyngeal Basaloid Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oropharyngeal Basaloid Carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0007351", "names": ["Macular coloboma", "macular coloboma", "Coloboma of macula", "AGENESIS OF MACULA", "COLOBOMA OF MACULA", "agenesis of macula", "coloboma of macula", "Agenesis of macula", "Coloboma of the macula", "Hereditary macular coloboma", "Congenital coloboma of macula lutea", "hereditary macular coloboma (subtype)", "Congenital coloboma of macula lutea (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coloboma of macula", "shortest_name_length": 16}
{"curie": "UMLS:C1266089", "names": ["Metaplastic Carcinoma", "Metaplastic carcinoma", "metaplastic carcinoma", "Metaplastic carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metaplastic carcinoma", "shortest_name_length": 21}
{"curie": "MONDO:0010814", "names": ["NNMS", "NIVELON-NIVELON-MABILLE SYNDROME", "Nivelon Nivelon Mabille syndrome", "Nivelon-Nivelon-Mabille syndrome", "Pseudohermaphrodism and chondrodysplasia", "chondrodysplasia-pseudohermaphrodism syndrome", "Chondrodysplasia pseudohermaphrodism syndrome", "Chondrodysplasia pseudohermaphroditism syndrome", "CHONDRODYSPLASIA-PSEUDOHERMAPHRODITISM SYNDROME", "chondrodysplasia-pseudohermaphroditism syndrome", "Chondrodysplasia-pseudohermaphroditism syndrome", "chondrodysplasia-disorder of sex development syndrome", "Chondrodysplasia-disorder of sex development syndrome", "Chondrodysplasia with disorder of sex development syndrome", "Chondrodysplasia with disorder of sex development syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chondrodysplasia-pseudohermaphroditism syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0006820", "names": ["Cortical necrosis", "necrosis; cortical", "cortical; necrosis", "Cortical necrosis NOS", "Kidney cortex necrosis", "NECROSIS KIDNEY CORTEX", "Necrosis kidney cortex", "Kidney Cortex Necrosis", "KIDNEY CORTEX NECROSIS", "kidney cortex necrosis", "Necrosis, Kidney Cortex", "Renal Cortical Necrosis", "Renal cortical necrosis", "RENAL CORTICAL NECROSIS", "renal cortical necrosis", "Necrosis, Renal Cortical", "Renal cortical necrosis NOS", "Necrosis of cortex of kidney", "Necrosis of the kidney cortex", "renal cortical necrosis (diagnosis)", "nephropathy renal cortical necrosis", "Nephropathy NOS with cortical necrosis", "Necrosis of cortex of kidney (disorder)", "Nephropathy NOS with renal cortical necrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kidney cortex necrosis", "shortest_name_length": 17}
{"curie": "MONDO:0000105", "names": ["anemia, nonspherocytic hemolytic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anemia, nonspherocytic hemolytic", "shortest_name_length": 32}
{"curie": "MONDO:0005754", "names": ["Grand mal", "grand mal", "Major Epilepsy", "Major epilepsy", "Epilepsy, Major", "EPILEPSY, MAJOR", "epilepsy; major", "Major convulsion", "major; epileptic", "Major Epilepsies", "grand mal seizure", "Epilepsy grand mal", "Grand mal epilepsy", "Epilepsy;grand mal", "EPILEPSY GRAND MAL", "grand mal epilepsy", "Grand Mal epilepsy", "grand Mal epilepsy", "Grand Mal Epilepsy", "grand mal; epilepsy", "EPILEPSY, GRAND MAL", "Epilepsy, Grand Mal", "epilepsy; grand mal", "CONVULSION GRAND MAL", "grand mal convulsion", "Grand Mal Convulsion", "Grand mal convulsion", "Convulsion grand mal", "GRAND MAL CONVULSION", "tonic-clonic epilepsy", "Convulsions grand mal", "Tonic-clonic epilepsy", "clonic epilepsy tonic", "Tonic-Clonic Epilepsy", "Convulsion, Grand Mal", "CONVULSIONS GRAND MAL", "Grand Mal Convulsions", "Epilepsy, Tonic-Clonic", "Convulsions, Grand Mal", "Epilepsy, Tonic Clonic", "Tonic-Clonic Epilepsies", "Tonic-clonic convulsion", "tonic clonic convulsion", "tonic-clonic convulsion", "Tonic Clonic Convulsion", "Convulsion, Tonic Clonic", "Clonic-tonic convulsions", "Tonic Clonic Convulsions", "Epilepsies, Tonic-Clonic", "Tonic/ clonic convulsions", "TONIC/ CLONIC CONVULSIONS", "Convulsions, Tonic Clonic", "Grand Mal Seizure Disorder", "Seizure Disorder, Grand Mal", "Major Motor Seizure Disorder", "disorders grand mal seizures", "Tonic Clonic Seizure Disorder", "Tonic Clonic Seizure Syndrome", "Tonic-clonic seizure syndrome", "SEIZURE DISORDER TONIC CLONIC", "grand mal seizure (diagnosis)", "Seizure Disorder, Major Motor", "Tonic-Clonic Seizure Disorder", "Tonic-Clonic Seizure Syndrome", "Syndrome, Tonic-Clonic Seizure", "Disorder, Tonic-Clonic Seizure", "Seizure Syndrome, Tonic-Clonic", "Seizure Disorder, Tonic-Clonic", "Seizure Disorder, Tonic Clonic", "Tonic-Clonic Seizure Syndromes", "Tonic-Clonic Seizure Disorders", "Seizure Disorders, Tonic-Clonic", "Seizure Syndromes, Tonic-Clonic", "Disorders, Tonic-Clonic Seizure", "Syndromes, Tonic-Clonic Seizure", "Tonic-Clonic Convulsion Disorder", "Tonic Clonic Convulsion Syndrome", "Tonic-Clonic Convulsion Syndrome", "Tonic-clonic epilepsy (disorder)", "epileptic seizures, tonic-clonic", "Epileptic seizures, tonic-clonic", "Tonic Clonic Convulsion Disorder", "Disorder, Tonic-Clonic Convulsion", "Convulsion Disorder, Tonic-Clonic", "Syndrome, Tonic-Clonic Convulsion", "Tonic-Clonic Convulsion Disorders", "Convulsion Syndrome, Tonic-Clonic", "tonic-clonic epilepsy (diagnosis)", "Tonic-Clonic Convulsion Syndromes", "Syndromes, Tonic-Clonic Convulsion", "Convulsion Disorders, Tonic-Clonic", "Convulsion Syndromes, Tonic-Clonic", "Disorders, Tonic-Clonic Convulsion", "PRIMARY GENERALIZED EPILEPSY, MAJOR", "generalized convulsive grand mal seizure", "generalized convulsive tonic-clonic seizure", "epilepsy with generalized tonic-clonic seizures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy with generalized tonic-clonic seizures", "shortest_name_length": 9}
{"curie": "MONDO:0009630", "names": ["MAC", "MCOPCB4", "Colobomatous microphthalmia", "Microphthalmia with colobomatous cyst", "MICROPHTHALMIA WITH COLOBOMATOUS CYST", "Microphthalmia With Colobomatous Cyst", "microphthalmia with colobomatous cyst", "MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 4", "microphthalmia, isolated, with coloboma 4", "Microphthalmia, Isolated, with Coloboma 4", "Microphthalmia-anophthalmia-coloboma syndrome", "microphthalmia, isolated, with coloboma type 4", "Microphthalmos co-occurrent with congenital ocular coloboma", "Microphthalmos co-occurrent with congenital ocular coloboma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microphthalmia, isolated, with coloboma 4", "shortest_name_length": 3}
{"curie": "MONDO:0021300", "names": ["oropharynx adenoid cystic carcinoma", "oropharyngeal adenoid cystic carcinoma", "adenoid cystic carcinoma of oropharynx", "Adenoid cystic carcinoma of oropharynx", "Adenoid Cystic Carcinoma of Oropharynx", "Oropharyngeal Adenoid Cystic Carcinoma", "oropharyngeal throat adenoid cystic cancer", "Adenoid Cystic Carcinoma of the Oropharynx", "Oropharyngeal Throat Adenoid Cystic Cancer", "adenoid cystic carcinoma of the oropharynx", "Adenoid cystic carcinoma of oropharynx (disorder)", "adenoid cystic carcinoma of oropharynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenoid cystic carcinoma of oropharynx", "shortest_name_length": 35}
{"curie": "UMLS:C2363734", "names": ["Placentomegaly", "Placental Hypertrophy", "Placental hypertrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Placental hypertrophy", "shortest_name_length": 14}
{"curie": "MONDO:0012230", "names": ["MYP10", "Myopia 10", "MYOPIA 10", "myopia 10", "MYOPIA 10 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopia 10", "shortest_name_length": 5}
{"curie": "MONDO:0006663", "names": ["HIE", "birth asphyxia", "Birth Asphyxia", "Birth asphyxia", "asphyxia birth", "Fetal Asphyxia", "fetal asphyxia", "birth; asphyxia", "Asphyxia - birth", "newborn asphyxia", "birth depression", "Birth Depression", "Asphyxia;newborn", "asphyxia - birth", "asphyxia newborn", "Asphyxia neonatal", "perinatal hypoxia", "neonatal asphyxia", "Neonatal asphyxia", "ASPHYXIA NEONATAL", "asphyxia; newborn", "asphyxia neonatal", "newborn; asphyxia", "asphyxia newborns", "Perinatal asphyxia", "postnatal asphyxia", "Perinatal Asphyxia", "asphyxia perinatal", "perinatal asphyxia", "hypoxia neonatorum", "asphyxia neonatorum", "Asphyxia neonatorum", "Asphyxia Neonatorum", "Perinatal Depression", "perinatal depression", "Intrapartum asphyxia", "intrapartum asphyxia", "Intrapartum Asphyxia", "Neonatal asphyxia, NOS", "Asphyxia of newborn NOS", "Birth asphyxia (disorder)", "Birth asphyxia (diagnosis)", "Intrapartum fetal asphyxia", "Asphyxia in liveborn infant", "Birth asphyxia, unspecified", "Intrapartum foetal asphyxia", "Asphyxia, in liveborn infant", "fetal hypoxia birth asphyxia", "asphyxia, in liveborn infant", "Perinatal asphyxia (disorder)", "Asphyxia NOS in liveborn infant", "hypoxic-ischemic encephalopathy", "Asphyxia, NOS, in liveborn infant", "Asphyxia in liveborn infant (disorder)", "neonatal hypoxic and ischemic brain injury", "hypoxic and ischemic brain injury in the newborn", "Unspecified severity of birth asphyxia in liveborn infant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "perinatal asphyxia", "shortest_name_length": 3}
{"curie": "MONDO:0008758", "names": ["AHD", "AHS", "PNDC", "Alpers", "MTDPS4A", "alper disease", "Alper Disease", "alper syndrome", "Alper Syndrome", "Poliodystrophy", "Alper syndrome", "alpers disease", "ALPER SYNDROME", "Alpers Disease", "Alpers disease", "Alpers Syndrome", "Alpers syndrome", "Alpers' Disease", "alper's disease", "alpers syndrome", "ALPERS SYNDROME", "Alpers' disease", "alpers' disease", "Alper's disease", "Alper's Disease", "Alper's Syndrome", "Syndrome, Alpers", "Alper's syndrome", "Alpers' Syndrome", "Disease, Alpers'", "Poliodystrophy, NOS", "Grey-matter degeneration", "Gray matter degeneration", "infantile poliodystrophy", "Grey matter degeneration", "grey matter; degeneration", "gray matter; degeneration", "degeneration; grey matter", "degeneration; gray matter", "Alpers Huttenlocher Disease", "Alpers' disease (diagnosis)", "Alpers Huttenlocher disease", "ALPERS-HUTTENLOCHER SYNDROME", "Alpers Huttenlocher syndrome", "Alpers-Huttenlocher syndrome", "Alpers Huttenlocher Syndrome", "Alpers-Huttenlocher Syndrome", "Syndrome, Alpers-Huttenlocher", "Spongy glioneuronal dystrophy", "Poliodystrophia cerebri progressiva", "progressive cerebral poliodystrophy", "progressive sclerosing poliodystrophy", "Progressive sclerosing poliodystrophy", "Progressive Sclerosing Poliodystrophy", "Diffuse Cerebral Sclerosis of Schilder", "mitochondrial DNA depletion syndrome 4a", "mitochondrial DNA depletion syndrome 4A", "Progressive Sclerosing Poliodystrophies", "diffuse cerebral degeneration in infancy", "Alpers' disease or gray-matter degeneration", "Alpers Progressive Infantile Poliodystrophy", "Alpers progressive infantile poliodystrophy", "ALPERS PROGRESSIVE INFANTILE POLIODYSTROPHY", "mitochondrial DNA depletion syndrome type 4a", "Alpers progressive sclerosing poliodystrophy", "Progressive degeneration, cerebral gray matter", "Progressive sclerosing poliodystrophy (disorder)", "mitochondrial DNA depletion syndrome 4A (Alpers type)", "MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)", "Progressive neuronal degeneration with liver cirrhosis", "Progressive Neuronal Degeneration of Childhood with Liver Disease", "progressive neuronal degeneration of childhood with liver disease", "Progressive neuronal degeneration of childhood with liver disease", "neuronal Degeneration of childhood with liver disease, progressive", "Neuronal Degeneration Of Childhood With Liver Disease, Progressive", "NEURONAL DEGENERATION OF CHILDHOOD WITH LIVER DISEASE, PROGRESSIVE", "Alpers diffuse Degeneration of cerebral Gray matter with hepatic cirrhosis", "ALPERS DIFFUSE DEGENERATION OF CEREBRAL GRAY MATTER WITH HEPATIC CIRRHOSIS", "Alpers Diffuse Degeneration of Cerebral Gray Matter with Hepatic Cirrhosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial DNA depletion syndrome 4a", "shortest_name_length": 3}
{"curie": "MONDO:0054752", "names": ["SYNS4", "multiple synostoses syndrome 4", "MULTIPLE SYNOSTOSES SYNDROME 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple synostoses syndrome 4", "shortest_name_length": 5}
{"curie": "UMLS:C1335938", "names": ["Secondary Chondrosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary Chondrosarcoma", "shortest_name_length": 24}
{"curie": "MONDO:0012757", "names": ["IMMUNODEFICIENCY, OVARIAN DYSGENESIS, AND PULMONARY FIBROSIS", "immunodeficiency, ovarian dysgenesis, and pulmonary fibrosis", "lung fibrosis-immunodeficiency-46,XX gonadal dysgenesis syndrome", "Lung fibrosis-immunodeficiency-46,XX gonadal dysgenesis syndrome", "Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome", "lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome", "Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome (disorder)", "lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung fibrosis-immunodeficiency-46,XX gonadal dysgenesis syndrome", "shortest_name_length": 60}
{"curie": "MONDO:0010109", "names": ["Madokoro Ohdo Sonoda syndrome", "tetra-amelia, ectodermal dysplasia, and lacrimal duct abnormality", "Tetraamelia With Ectodermal Dysplasia And Lacrimal Duct Abnormalities", "TETRAAMELIA WITH ECTODERMAL DYSPLASIA AND LACRIMAL DUCT ABNORMALITIES", "tetraamelia with ectodermal dysplasia and lacrimal duct abnormalities", "Tetra amelia with ectodermal dysplasia and lacrimal duct abnormalities", "Absence of all four limbs with ectodermal dysplasia and lacrimal duct abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tetraamelia with ectodermal dysplasia and lacrimal duct abnormalities", "shortest_name_length": 29}
{"curie": "UMLS:C5447973", "names": ["Refractory Malignant Salivary Gland Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Malignant Salivary Gland Neoplasm", "shortest_name_length": 44}
{"curie": "MONDO:0012660", "names": ["KAZA2", "kala-AZAR, susceptibility to, 2", "KALA-AZAR, SUSCEPTIBILITY TO, 2", "susceptibility to visceral leishmaniasis, 2", "leishmaniasis, visceral, susceptibility to, 2", "LEISHMANIASIS, VISCERAL, SUSCEPTIBILITY TO, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "susceptibility to visceral leishmaniasis, 2", "shortest_name_length": 5}
{"curie": "MONDO:0013575", "names": ["Plasma fibronectin deficiency", "plasma fibronectin deficiency", "PLASMA FIBRONECTIN DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "plasma fibronectin deficiency", "shortest_name_length": 29}
{"curie": "MONDO:0011274", "names": ["MNKES", "Muenke syndrome", "MUENKE SYNDROME", "muenke syndrome", "Muenke Syndrome", "Muenke syndrome (disorder)", "muenke syndrome (diagnosis)", "FGFR3-related craniosynostosis", "FGFR3-Related Craniosynostosis", "FGFR3-Associated Coronal Synostosis", "Syndrome of coronal craniosynostosis", "syndrome of coronal craniosynostosis", "MUENKE NONSYNDROMIC CORONAL CRANIOSYNOSTOSIS", "Muenke nonsyndromic coronal craniosynostosis", "Fibroblast growth factor receptor 3-related craniosynostosis", "Fibroblast growth factor receptor 3 (FGFR3) related craniosynostosis", "Fibroblast growth factor receptor 3-related craniosynostosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Muenke syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0013297", "names": ["LGMD1H", "muscular dystrophy limb-girdle type 1H", "limb-girdle muscular dystrophy type 1H", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1H", "muscular dystrophy, limb-girdle, type 1H", "Autosomal dominant limb-girdle muscular dystrophy type 1H", "autosomal dominant limb-girdle muscular dystrophy type 1H", "Autosomal dominant limb-girdle muscular dystrophy type 1H (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant limb-girdle muscular dystrophy type 1H", "shortest_name_length": 6}
{"curie": "MONDO:0016719", "names": ["Microcephaly seizures mental retardation heart disorders", "microcephaly seizures mental retardation heart disorders", "microcephaly seizures intellectual disability heart disorders", "microcephaly-seizures-intellectual disability-heart disease syndrome", "microcephaly, seizures, mental retardation, congenital heart disease, and skeletal abnormalities", "Microcephaly, seizures, mental retardation, congenital heart disease, and skeletal abnormalities", "microcephaly, seizures, intellectual disability, congenital heart disease, and skeletal abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly-seizures-intellectual disability-heart disease syndrome", "shortest_name_length": 56}
{"curie": "MONDO:0018216", "names": ["KDVS", "KdVS", "Koolen Syndrome", "Del(17)(q21.31)", "Monosomy 17q21.31", "monosomy 17q21.31", "Koolen De Vries syndrome", "Koolen de Vries syndrome", "Koolen-De Vries syndrome", "KOOLEN-DE VRIES SYNDROME", "Koolen-De Vries Syndrome", "17q21.31 Deletion Syndrome", "17q21.31 Microdeletion Syndrome", "Microdeletion 17q21.31 Syndrome", "17q21.31 microdeletion syndrome", "MICRODELETION 17q21.31 SYNDROME", "Koolen De Vries syndrome (disorder)", "Chromosome 17q21.31 Deletion Syndrome", "CHROMOSOME 17q21.31 DELETION SYNDROME", "17q21.31 recurrent microdeletion syndrome", "Chromosome 17q21.31 Microdeletion Syndrome", "KANSL1-related intellectual disability syndrome", "Koolen-de Vries syndrome due to 17q21.31 microdeletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Koolen-de Vries syndrome due to 17q21.31 microdeletion syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C4054386", "names": ["Hepatitis B Virus Associated Nephrotic Syndrome", "Nephrotic Syndrome - Hepatitis B Virus Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - Hepatitis B Virus Associated", "shortest_name_length": 47}
{"curie": "MONDO:0021091", "names": ["Papillary cystadenoma", "papillary cystadenoma", "Papillary Cystadenoma", "Cystadenoma, Papillary", "Papillary Cystadenomas", "Cystadenomas, Papillary", "Papillary cystadenoma NOS", "Papillary cystadenoma, NOS", "CYSTADENOMA, PAPILLARY, BENIGN", "cystadenoma, papillary, benign", "cystadenoma; papillary, unspecified site", "papillary; cystadenoma, unspecified site", "Papillary cystadenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papillary cystadenoma", "shortest_name_length": 21}
{"curie": "MONDO:0016996", "names": ["NK-cell enteropathy", "Natural killer cell enteropathy", "NK (natural killer) cell enteropathy", "Natural killer cell enteropathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "NK-cell enteropathy", "shortest_name_length": 19}
{"curie": "UMLS:C5670002", "names": ["Hematologic Toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hematologic Toxicity", "shortest_name_length": 20}
{"curie": "MONDO:0010858", "names": ["Fryns Macrocephaly", "Fryns macrocephaly", "FRYNS MACROCEPHALY", "Macrocephaly-spastic paraplegia-dysmorphism syndrome", "macrocephaly-spastic paraplegia-dysmorphism syndrome", "Macrocephaly with spastic paraplegia and dysmorphism syndrome", "Macrocephaly with spastic paraplegia and dysmorphism syndrome (disorder)", "MACROCEPHALY WITH SPASTIC PARAPLEGIA AND DISTINCTIVE CRANIOFACIAL APPEARANCE", "Macrocephaly with Spastic Paraplegia and Distinctive Craniofacial Appearance", "macrocephaly with spastic paraplegia and distinctive craniofacial appearance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macrocephaly-spastic paraplegia-dysmorphism syndrome", "shortest_name_length": 18}
{"curie": "MONDO:0019946", "names": ["conjunctivitis lignosa", "Ligneous conjunctivitis", "ligneous conjunctivitis", "Ligneous Conjunctivitis", "LIGNEOUS CONJUNCTIVITIS", "Ligneous conjunctivitis (disorder)", "ligneous conjunctivitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ligneous conjunctivitis", "shortest_name_length": 22}
{"curie": "MONDO:0013351", "names": ["postnatal progressive microcephaly, seizures, and brain atrophy", "MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY", "microcephaly, postnatal progressive, with seizures and brain atrophy", "infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly", "shortest_name_length": 63}
{"curie": "MONDO:0018546", "names": ["Serotonin storm", "serotonin storm", "syndrome serotonin", "SEROTONIN SYNDROME", "Serotonin Syndrome", "serotonin syndrome", "serotonin toxicity", "Serotonin toxicity", "Serotonin syndrome", "Serotonin Syndromes", "Serotonin toxidrome", "Syndrome, Serotonin", "serotonin toxidrome", "serotonin syndromes", "Syndromes, Serotonin", "Serotonergic syndrome", "serotonergic syndrome", "serotonin syndrome toxicity", "Serotonin syndrome (disorder)", "serotonin syndrome toxicity (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "serotonin syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0013632", "names": ["DFNA33", "autosomal dominant deafness 33", "deafness, autosomal dominant 33", "DEAFNESS, AUTOSOMAL DOMINANT 33", "autosomal dominant nonsyndromic deafness 33", "autosomal dominant nonsyndromic hearing loss 33", "autosomal dominant nonsyndromic deafness type 33"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 33", "shortest_name_length": 6}
{"curie": "MONDO:0012310", "names": ["EXTERNAL OPHTHALMOPLEGIA WITH SYNERGISTIC DIVERGENCE", "External Ophthalmoplegia with Synergistic Divergence", "external ophthalmoplegia with synergistic divergence", "congenital fibrosis syndrome with synergistic divergence", "Congenital Fibrosis Syndrome with Synergistic Divergence", "CONGENITAL FIBROSIS SYNDROME WITH SYNERGISTIC DIVERGENCE", "fibrosis of extraocular muscles, congenital, with synergistic divergence", "FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, WITH SYNERGISTIC DIVERGENCE", "EXTERNAL OPHTHALMOPLEGIA, SYNERGISTIC DIVERGENCE, JAW WINKING, AND OCULOCUTANEOUS HYPOPIGMENTATION", "external ophthalmoplegia, synergistic divergence, jaw winking, and oculocutaneous hypopigmentation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibrosis of extraocular muscles, congenital, with synergistic divergence", "shortest_name_length": 52}
{"curie": "MONDO:0011576", "names": ["FH2", "FH 2", "FHII", "FH-II", "FH II", "HALD2", "familial adrenal adenoma", "Familial adrenal adenoma", "Familial hyperaldosteronism type 2", "Familial Hyperaldosteronism Type 2", "familial hyperaldosteronism type 2", "Familial hyperaldosteronism type II", "familial hyperaldosteronism type II", "Hyperaldosteronism, Familial, Type II", "HYPERALDOSTERONISM, FAMILIAL, TYPE II", "hyperaldosteronism, familial, type II", "Familial hyperaldosteronism type 2 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial hyperaldosteronism type II", "shortest_name_length": 3}
{"curie": "MONDO:0016014", "names": ["fetal minoxidil syndrome", "Fetal minoxidil syndrome", "Foetal minoxidil syndrome", "minoxidil antenatal exposure", "Minoxidil antenatal infection", "minoxidil antenatal infection", "Fetal minoxidil syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fetal minoxidil syndrome", "shortest_name_length": 24}
{"curie": "UMLS:C1167868", "names": ["Perinephric collection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perinephric collection", "shortest_name_length": 22}
{"curie": "UMLS:C0011265", "names": ["dementia", "Dementia presenile", "Presenile dementia", "presenile dementia", "dementia presenile", "Presenile Dementia", "DEMENTIA PRESENILE", "pre senile dementia", "Pre-Senile Dementia", "pre-senile dementia", "Dementia, Presenile", "dementia; presenile", "presenile psychosis", "presenile; dementia", "Pre-senile dementia", "Psychosis;presenile", "DEMENTIA, PRESENILE", "presenile; psychosis", "Dementia (Presenile)", "psychosis; presenile", "Presenile dementia NOS", "Presenile dementia, NOS", "Presenile psychosis NOS", "Presenile dementia (disorder)", "presenile dementia (diagnosis)", "presenile organic psychotic conditions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Presenile dementia", "shortest_name_length": 8}
{"curie": "MONDO:0020489", "names": ["FHHA1", "CMO I", "CMO II", "18-oxidase deficiency", "18-hydroxylase deficiency", "Aldosterone Synthase Deficiency", "aldosterone synthase deficiency", "Corticosterone Methyl Oxidase Deficiency", "corticosterone methyloxidase deficiency type I", "familial hyperreninemic hypoaldosteronism type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial hyperreninemic hypoaldosteronism type 1", "shortest_name_length": 5}
{"curie": "UMLS:C1332255", "names": ["Ampullary Villous Adenoma", "Ampulla of Vater Villous Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ampulla of Vater Villous Adenoma", "shortest_name_length": 25}
{"curie": "MONDO:0044767", "names": ["pheochromocytoma, childhood", "childhood adrenal gland pheochromocytoma", "Childhood Adrenal Gland Pheochromocytoma", "malignant pediatric adrenal gland pheochromocytoma", "malignant childhood adrenal gland pheochromocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood adrenal gland pheochromocytoma", "shortest_name_length": 27}
{"curie": "MONDO:0012799", "names": ["CMH11", "hypertrophic cardiomyopathy 11", "cardiomyopathy, hypertrophic, 11", "ACTC1 hypertrophic cardiomyopathy", "hypertrophic cardiomyopathy type 11", "cardiomyopathy familial hypertrophic 11", "cardiomyopathy, familial hypertrophic, 11", "Cardiomyopathy, Familial Hypertrophic, 11", "CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 11", "Familial Hypertrophic Cardiomyopathy Type 11", "cardiomyopathy, familial hypertrophic, type 11", "hypertrophic cardiomyopathy caused by mutation in ACTC1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophic cardiomyopathy 11", "shortest_name_length": 5}
{"curie": "UMLS:C1334667", "names": ["Mediastinal MPNST", "MPNST of Mediastinum", "MPNST of mediastinum", "MPNST of the Mediastinum", "Mediastinal Malignant Peripheral Nerve Sheath Tumor", "Malignant Mediastinal Peripheral Nerve Sheath Tumor", "Malignant Peripheral Nerve Sheath Tumor of Mediastinum", "Malignant Mediastinal Peripheral Nerve Sheath Neoplasm", "Malignant Peripheral Nerve Sheath Neoplasm of Mediastinum", "Malignant Peripheral Nerve Sheath Tumor of the Mediastinum", "Malignant Peripheral Nerve Sheath Neoplasm of the Mediastinum", "malignant peripheral nerve sheath tumor (MPNST) of mediastinum", "malignant peripheral nerve sheath tumor (MPNST) of mediastinum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant peripheral nerve sheath tumor (MPNST) of mediastinum", "shortest_name_length": 17}
{"curie": "UMLS:C0405106", "names": ["Retained fetal membrane", "Retained placenta or membranes", "Retained placenta and membranes", "retained placenta and membranes", "Retained fetal membrane (disorder)", "Retained placenta and membranes (disorder)", "retained placenta and membranes (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retained placenta and membranes (disorder)", "shortest_name_length": 23}
{"curie": "MONDO:0005908", "names": ["PPR infection", "Pseudorinderpest", "Peste des petits ruminants", "Peste-des-Petits-Ruminants", "Peste des Petits Ruminants", "Peste des petits ruminants Infection", "Peste des petits ruminants (disorder)", "peste des petits ruminants infectious disease", "Small ruminant morbillivirus infectious disease", "Small ruminant morbillivirus disease or disorder", "Small ruminant morbillivirus caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peste des petits ruminants infectious disease", "shortest_name_length": 13}
{"curie": "UMLS:C4763427", "names": ["Unresectable Adrenal Gland Pheochromocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Adrenal Gland Pheochromocytoma", "shortest_name_length": 43}
{"curie": "MONDO:8000003", "names": ["streptococcus pneumoniae discitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "streptococcus pneumoniae discitis", "shortest_name_length": 33}
{"curie": "UMLS:C0861843", "names": ["Carcinoma duodenum resectable", "Resectable Duodenal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carcinoma duodenum resectable", "shortest_name_length": 29}
{"curie": "MONDO:0004946", "names": ["Hypoglycemia", "HYPOGLYCEMIA", "hypoglycemia", "hypoglycaemia", "Hypoglycaemia", "HYPOGLYCAEMIA", "Low Blood Sugar", "Low blood sugar", "blood sugar; low", "hypoglycemia nos", "low; blood sugar", "Hypoglycemia NOS", "sugar; blood, low", "Hypoglycemia, NOS", "Hypoglycaemia NOS", "low blood glucose", "blood; sugar, low", "glucose, Low blood", "Hypoglycaemia, NOS", "blood glucose, Low", "Hypoglycemic disorder", "Hypoglycemic syndrome", "low blood sugar level", "hypoglycemic disorder", "Hypoglycaemic disorder", "Hypoglycaemic syndrome", "Hypoglycemia (disorder)", "hypoglycemia (diagnosis)", "Hypoglycemia, unspecified", "Hypoglycaemia, unspecified", "Hypoglycemic syndrome, NOS", "Hypoglycaemic syndrome, NOS", "Hypoglycemic disorder (disorder)", "Hypoglycemic syndrome (disorder)", "hypoglycemic disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypoglycemia", "shortest_name_length": 12}
{"curie": "MONDO:0017284", "names": ["dup(X)(p22)", "Duplication Xp22", "dup(X)(p22.13p22.2)", "Xp22.13p22.2 duplication syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Xp22.13p22.2 duplication syndrome", "shortest_name_length": 11}
{"curie": "UMLS:C1710641", "names": ["Vulvar Angiomyofibroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Angiomyofibroblastoma", "shortest_name_length": 28}
{"curie": "UMLS:C0856697", "names": ["Tuberculous Bronchopneumonia", "Tuberculous bronchopneumonia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tuberculous bronchopneumonia", "shortest_name_length": 28}
{"curie": "UMLS:C1698088", "names": ["Malignant solid tumor", "Malignant Solid Tumor", "Malignant solid tumour", "Malignant Solid Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Solid Neoplasm", "shortest_name_length": 21}
{"curie": "UMLS:C0238706", "names": ["Right atrial hypertrophy", "ATRIAL HYPERTROPHY, RIGHT", "Right atrial hypertrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Right atrial hypertrophy", "shortest_name_length": 24}
{"curie": "MONDO:0011036", "names": ["Bonnemann-Meinecke syndrome", "Bonnemann Meinecke syndrome", "Porencephaly cerebellar hypoplasia malformations", "porencephaly cerebellar hypoplasia internal malformations", "porencephaly, cerebellar hypoplasia, and internal malformations", "Porencephaly, cerebellar hypoplasia, and internal malformations", "PORENCEPHALY, CEREBELLAR HYPOPLASIA, AND INTERNAL MALFORMATIONS", "Porencephaly-cerebellar hypoplasia-internal malformations syndrome", "porencephaly-cerebellar hypoplasia-internal malformations syndrome", "Porencephaly, cerebellar hypoplasia, internal malformations syndrome", "Porencephaly, cerebellar hypoplasia, internal malformations syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "porencephaly-cerebellar hypoplasia-internal malformations syndrome", "shortest_name_length": 27}
{"curie": "UMLS:C1336478", "names": ["Stage I Renal Pelvis and Ureter Cancer", "Stage I Renal Pelvis and Ureter Carcinoma", "Stage I Renal Pelvis and Ureter Cancer AJCC v7", "Stage I Renal Pelvis and Ureter Carcinoma AJCC v7", "stage I transitional cell cancer of the renal pelvis and ureter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Renal Pelvis and Ureter Cancer AJCC v7", "shortest_name_length": 38}
{"curie": "UMLS:C0333987", "names": ["Mesothelial hyperplasia", "Mesothelial Hyperplasia", "Hyperplasia, mesothelial", "Mesothelial hyperplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mesothelial hyperplasia", "shortest_name_length": 23}
{"curie": "UMLS:C0151713", "names": ["Hyperacidity", "HYPERACIDITY", "hyperacidity", "Hyperchlorhydria", "gastrosuccorrhea", "hyperchlorhydria", "HYPERCHLORHYDRIA", "gastric hyperacidity", "Gastric hyperacidity", "Hyperacidity, gastric", "Gastric acid increased", "Increased gastric acidity", "Hyperchlorhydria, gastric", "Gastric acidity, increased", "Hyperchlorhydria (disorder)", "hyperchlorhydria (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyperchlorhydria", "shortest_name_length": 12}
{"curie": "MONDO:0100082", "names": ["LPRD1", "LEOPARD SYNDROME 1", "Leopard Syndrome 1", "LEOPARD syndrome 1", "LEOPARD Syndrome, 1", "LEOPARD syndrome type 1", "multiple lentigines syndrome", "lentiginosis, cardiomyopathic", "Noonan syndrome with multiple lentigines 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "LEOPARD syndrome 1", "shortest_name_length": 5}
{"curie": "UMLS:C0233746", "names": ["Perception Disturbance", "Perceptual disturbance", "perceptual disturbance", "perceptual disturbances", "disturbances perception", "Perceptual Disturbances", "Disturbance of perception", "Disturbance of perception, NOS", "perceptual disturbances (physical finding)", "cognitive functions perceptual disturbances"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perceptual disturbance", "shortest_name_length": 22}
{"curie": "MONDO:0006233", "names": ["gonadal teratoma", "Gonadal Teratoma", "Teratoma, Gonads", "teratoma, gonads"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gonadal teratoma", "shortest_name_length": 16}
{"curie": "MONDO:0023006", "names": ["doxorubicin induced cardiomyopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "doxorubicin induced cardiomyopathy", "shortest_name_length": 34}
{"curie": "UMLS:C0013985", "names": ["Disturbance;emotional", "disturbance emotional", "emotional disturbance", "Emotional Disturbance", "Emotional disturbance", "Disturbance, Emotional", "Emotional Disturbances", "emotional disturbances", "Disturbances, Emotional", "Emotional disturbance NOS", "emotional disturbance (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Emotional Disturbances", "shortest_name_length": 21}
{"curie": "MONDO:0001302", "names": ["heart; hypertension", "Hypertensive cardiopathy", "cardiopathy hypertensive", "hypertensive cardiopathy", "Hypertensive Cardiomegaly", "hypertensive cardiomegaly", "Hypertensive cardiomegaly", "hypertension heart disease", "Hypertension;heart disease", "heart disease hypertension", "Hypertensive Heart Disease", "HYPERTENSIVE HEART DISEASE", "Hypertensive heart disease", "hypertensive heart disease", "Hypertensive Heart Diseaase", "diseases heart hypertensive", "Hypertensive heart disease NOS", "Hypertensive heart disease, NOS", "HHD - hypertensive heart disease", "HHD - Hypertensive heart disease", "Cardiomegaly due to hypertension", "HYPERTENSIVE CARDIOVASCULAR DISEASE", "Hypertensive cardiovascular disease", "hypertensive cardiovascular disease", "Hypertensive heart disease (disorder)", "Unspecified hypertensive heart disease", "hypertensive heart disease (diagnosis)", "Hypertensive heart disease, unspecified", "Cardiomegaly due to hypertension (disorder)", "hypertensive heart disease with cardiomegaly", "hypertensive heart disease with cardiomegaly (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertensive heart disease", "shortest_name_length": 19}
{"curie": "MONDO:0020345", "names": ["presynaptic congenital myasthenic syndrome", "presynaptic congenital myasthenic syndromes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "presynaptic congenital myasthenic syndrome", "shortest_name_length": 42}
{"curie": "MONDO:0007603", "names": ["Felty", "FELTY SYNDROME", "Felty syndrome", "felty syndrome", "Felty Syndrome", "Feltys Syndrome", "feltys syndrome", "Syndrome, Felty", "FELTYS SYNDROME", "Felty's syndrome", "Felty's Syndrome", "felty's syndrome", "Syndrome, Felty's", "familial Felty's syndrome", "Felty's syndrome (disorder)", "Felty's syndrome (diagnosis)", "Felty's syndrome, site unspecified", "Felty's syndrome, unspecified site", "Rheumatoid arthritis-hypersplenism syndrome", "Rheumatoid arthritis, leucopenia AND splenomegaly", "Rheumatoid arthritis, leukopenia and splenomegaly", "Rheumatoid arthritis, leukopenia AND splenomegaly", "rheumatoid arthritis, splenomegaly and neutropenia", "splenomegaly-neutropenia-rheumatoid arthritis syndrome", "Splenomegaly-neutropenia-rheumatoid arthritis syndrome", "Rheumatoid arthritis with splenoadenomegaly and leukopenia", "rheumatoid arthritis with splenoadenomegaly and leukopenia", "rheumatoid; arthritis, with splenoadenomegaly and leukopenia", "arthritis; rheumatoid, with splenoadenomegaly and leukopenia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Felty syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C1514948", "names": ["Stage IV High Grade Burkitt-Like Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV High Grade Burkitt-Like Lymphoma", "shortest_name_length": 41}
{"curie": "MONDO:0011502", "names": ["WFS2", "WOLFRAM SYNDROME 2", "Wolfram syndrome 2", "Wolfram Syndrome 2", "WOLFRAM syndrome 2", "CISD2 Wolfram syndrome", "Wolfram syndrome type 2", "Wolfram syndrome caused by mutation in CISD2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wolfram syndrome 2", "shortest_name_length": 4}
{"curie": "UMLS:C4505390", "names": ["Heroin Smoking", "Smoking, Heroin", "Heroin Smokings"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Heroin Smoking", "shortest_name_length": 14}
{"curie": "MONDO:0020355", "names": ["coloboma of eye lens"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coloboma of eye lens", "shortest_name_length": 20}
{"curie": "UMLS:C0392180", "names": ["Necrosis placenta", "NECROSIS PLACENTA", "Placental necrosis", "necrosis; placenta", "Placental Necrosis", "placenta; necrosis", "necrosis of placenta", "Necrosis of placenta", "Necrosis of placenta (disorder)", "necrosis of placenta (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Necrosis of placenta", "shortest_name_length": 17}
{"curie": "MONDO:0017359", "names": ["3-Methylglutaconicaciduria", "3-Methylglutaconic Aciduria", "3-Methylglutaconic aciduria", "3-methylglutaconic aciduria", "3-@METHYLGLUTACONIC ACIDURIA", "3mga (3-Methylglutaconic Aciduria)", "3-Methylglutaconic aciduria (disorder)", "3-methylglutaconic aciduria (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "3-methylglutaconic aciduria", "shortest_name_length": 26}
{"curie": "UMLS:C3850157", "names": ["Metabolic Side Effects of Drugs and Substances"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metabolic Side Effects of Drugs and Substances", "shortest_name_length": 46}
{"curie": "MONDO:0010549", "names": ["CMT2", "CMTX", "CMTX1", "Cmtx1", "CMT1X", "CMTX 1", "CMT2, FORMERLY", "CMT2, formerly", "HMSN, X-linked", "HMSN, X-LINKED", "Charcot Marie Tooth disease X-linked 1", "GJB1 Charcot-Marie-Tooth disease type X", "Charcot-Marie-Tooth neuropathy X type 1", "Charcot-Marie-Tooth Neuropathy X Type 1", "Charcot-Marie-Tooth disease, X-linked, 1", "X-linked Charcot-Marie-Tooth disease type 1", "CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1", "Charcot-Marie-Tooth neuropathy, X-linked, 1", "Charcot-Marie-Tooth Neuropathy, X-Linked, 1", "Charcot-Marie-Tooth disease X-linked, 1 (CMTX1)", "Charcot-Marie-Tooth disease X-linked dominant 1", "HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED", "Hereditary motor and sensory neuropathy, X-linked", "CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1", "Charcot-Marie-Tooth disease, X-linked dominant, 1", "hereditary motor and sensory neuropathy, X-linked", "Charcot-Marie-Tooth neuropathy X-linked dominant 1", "Charcot-Marie-Tooth disease X-linked dominant type 1", "Charcot-Marie-Tooth disease, X-linked dominant, type 1", "X-linked Charcot-Marie-Tooth disease type 1 (disorder)", "Charcot-Marie-Tooth peroneal muscular atrophy, X-linked", "CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED", "Charcot-Marie-Tooth disease X-linked, 1 (CMTX1) (diagnosis)", "Charcot-Marie-Tooth disease type X caused by mutation in GJB1", "Charcot-Marie-Tooth neuropathy, X-linked dominant, 1, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease X-linked dominant 1", "shortest_name_length": 4}
{"curie": "UMLS:C0015398", "names": ["eye disease hereditary", "Hereditary Eye Disease", "Eye Disease, Hereditary", "Hereditary Eye Diseases", "hereditary eye diseases", "Eye Diseases, Hereditary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eye Diseases, Hereditary", "shortest_name_length": 22}
{"curie": "UMLS:C0205696", "names": ["anaplastic carcinoma", "Anaplastic carcinoma", "carcinoma anaplastic", "Anaplastic Carcinoma", "Anaplastic Carcinomas", "Carcinoma, Anaplastic", "Carcinoma, anaplastic", "anaplastic carcinomas", "Carcinoma, anaplastic NOS", "Carcinoma, anaplastic type", "Carcinoma, anaplastic, NOS", "anaplastic carcinoma (diagnosis)", "Carcinoma, anaplastic (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anaplastic carcinoma", "shortest_name_length": 20}
{"curie": "UMLS:C0271852", "names": ["Hypercalcemia due to hyperthyroidism", "Hypercalcaemia due to hyperthyroidism", "Hypercalcemia due to hyperthyroidism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypercalcemia due to hyperthyroidism", "shortest_name_length": 36}
{"curie": "MONDO:0015636", "names": ["Dirofilariasis", "DIROFILARIASIS", "Dirofilariases", "dirofilariosis", "Dirofilariosis", "dirofilariasis", "Heartworm Disease", "heartworm disease", "Disease, Heartworm", "Dirofilaria infection", "infection; Dirofilaria", "Dirofilaria; infection", "infection by Dirofilaria", "Infection by Dirofilaria", "dirofilariasis (diagnosis)", "Infection by Dirofilaria, NOS", "Dirofilaria infectious disease", "Dirofilaria disease or disorder", "Infection caused by Dirofilaria", "Dirofilaria caused disease or disorder", "Infection caused by Dirofilaria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dirofilariasis", "shortest_name_length": 14}
{"curie": "UMLS:C1112626", "names": ["Allergic exanthema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Allergic exanthema", "shortest_name_length": 18}
{"curie": "MONDO:0006345", "names": ["Dupuytren", "Palmar fibromatosis", "Palmar Fibromatosis", "palmar fibromatosis", "fibromatosis palmar", "fibromatosis; palmar", "palmar; fibromatosis", "dupuytren contracture", "DUPUYTREN CONTRACTURE", "contracture dupuytren", "CONTRACTURE DUPUYTREN", "Dupuytren Contracture", "Dupuytren contracture", "Dupuytrens contracture", "Contracture, Dupuytren", "Dupuytren contractures", "DUPUYTRENS CONTRACTURE", "Dupuytren; contracture", "dupytren's contracture", "dupuytrens contracture", "contractures dupuytren", "contracture; Dupuytren", "CONTRACTURE DUPYTREN'S", "Dupuytrens Contracture", "contracture dupuytren's", "dupuytren's contracture", "Dupuytren's contracture", "contractures dupuytrens", "Dupuytren's Contracture", "DUPUYTREN'S CONTRACTURE", "Contracture, Dupuytren's", "contractures dupuytren's", "contracture dupuytrens's", "Fibromatosis, Dupuytren's", "Dupuytren disease of palm", "Palmar fascial fibromatosis", "Dupuytren's disease of palm", "fascia palmaris; retraction", "retraction; fascia palmaris", "Contracture of palmar fascia", "Dupuytren's contracture of hand", "Dupuytren contracture (disease)", "Dupuytren's contracture syndrome", "Hand(s) Dupuytrens Contracture(s)", "palmar part of manus fibromatosis", "Dupuytren's contracture (disorder)", "Dupuytren's contracture (diagnosis)", "Dupuytren's contracture was observed", "Dupuytren's disease of palm (disorder)", "Contracture of palmar fascia (disorder)", "Dupuytren's disease of palm (diagnosis)", "Palmar fascial fibromatosis [Dupuytren]", "Dupuytren's contracture (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "palmar fibromatosis", "shortest_name_length": 9}
{"curie": "UMLS:C0031094", "names": ["Periodontal pocket", "PERIODONTAL POCKET", "Periodontal Pocket", "periodontal pocket", "Periodontal Pockets", "Pocket, Periodontal", "periodontal pockets", "Periodontal pockets", "Pockets, Periodontal", "Periodontal pocketing", "Periodontal pocket deepened", "Periodontal pocket (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Periodontal Pocket", "shortest_name_length": 18}
{"curie": "UMLS:C0454655", "names": ["semantic pragmatic disorder", "semantic-pragmatic disorder", "Semantic-Pragmatic Disorder", "Semantic-pragmatic disorder", "Semantic Pragmatic Disorder", "Semantic-Pragmatic Disorders", "Semantic-pragmatic disorder (disorder)", "Semantic-pragmatic disorder (diagnosis)", "communication disorder speech and language semantic-pragmatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Semantic-Pragmatic Disorder", "shortest_name_length": 27}
{"curie": "MONDO:0013939", "names": ["PBD7B", "Peroxisome Biogenesis Disorder 7B", "PEROXISOME BIOGENESIS DISORDER 7B", "peroxisome biogenesis disorder 7B", "peroxisome biogenesis disorder type 7B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder 7B", "shortest_name_length": 5}
{"curie": "MONDO:0005520", "names": ["RICKETS", "Rickets", "RICKETT", "rickets", "rachitis", "Rachitis", "ricketts", "Rachitides", "Rickets NOS", "Rickets, NOS", "active rickets", "hypovitaminosis d", "hypovitaminosis D", "rickets (disease)", "Hypovitaminosis D", "HYPOVITAMINOSIS D", "Rickets (disorder)", "Weak and soft bones", "rickets (diagnosis)", "nutritional rickets", "Infantile osteomalacia", "osteomalacia; infantile", "infantile; osteomalacia", "OSTEOMALACIA, INFANTILE", "vitamin-D deficiency rickets", "vitamin D deficiency disease", "Vitamin D deficiency disease", "vitamin D hydroxylation-deficient rickets"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rickets", "shortest_name_length": 7}
{"curie": "UMLS:C4289946", "names": ["Ph1-Negative ALL", "Philadelphia-Negative ALL", "Philadelphia Chromosome Negative ALL", "Ph1-Negative Acute Lymphoblastic Leukemia", "Philadelphia-Negative Acute Lymphoblastic Leukemia", "Philadelphia Chromosome Negative Acute Lymphoblastic Leukemia", "Acute Lymphoblastic Leukemia, Philadelphia Chromosome Negative", "B Acute Lymphoblastic Leukemia, Philadelphia Chromosome Negative", "Precursor B Lymphoblastic Leukemia, Philadelphia Chromosome Negative", "Precursor B-Lymphoblastic Leukemia, Philadelphia Chromosome Negative", "B-Cell Acute Lymphoblastic Leukemia, Philadelphia Chromosome Negative"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B Acute Lymphoblastic Leukemia, Philadelphia Chromosome Negative", "shortest_name_length": 16}
{"curie": "MONDO:0013484", "names": ["CATC4", "CTRCT36", "cataract 36", "CATARACT 36", "cataract type 36", "TDRD7 cataract (disease)", "autosomal recessive congenital cataract 4", "cataract, autosomal recessive congenital 4", "CATARACT, AUTOSOMAL RECESSIVE CONGENITAL 4", "cataract (disease) caused by mutation in TDRD7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 36", "shortest_name_length": 5}
{"curie": "MONDO:0019541", "names": ["non-infectious choroiditis", "non-infectious posterior uveitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-infectious posterior uveitis", "shortest_name_length": 26}
{"curie": "MONDO:0011675", "names": ["CMTDIA", "CMT2GG", "Di-Cmta", "DI-CMTA", "CMTDIA, FORMERLY", "DI-CMTA, FORMERLY", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2GG", "Charcot-Marie-Tooth Disease, axonal, type 2GG", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2GG", "Charcot-Marie-Tooth disease dominant intermediate A", "Charcot-Marie-Tooth disease, dominant intermediate A", "Charcot-Marie-Tooth Disease, Dominant Intermediate A", "Charcot-Marie-Tooth neuropathy dominant intermediate A", "Charcot-Marie-Tooth neuropathy, dominant Intermediate a", "Charcot-Marie-Tooth Neuropathy, Dominant Intermediate A", "Charcot-Marie-Tooth disease dominant intermediate type A", "CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE A, FORMERLY", "CHARCOT-MARIE-TOOTH NEUROPATHY, DOMINANT INTERMEDIATE A, FORMERLY", "autosomal dominant intermediate Charcot-Marie-Tooth disease type A", "Autosomal dominant intermediate Charcot-Marie-Tooth disease type A", "Charcot-Marie-Tooth disease autosomal dominant intermediate type A", "Autosomal dominant intermediate Charcot-Marie-Tooth disease type A (disorder)", "Autosomal dominant intermediate Charcot-Marie-Tooth disease type A (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth Disease, axonal, type 2GG", "shortest_name_length": 6}
{"curie": "MONDO:0019157", "names": ["RARS", "AISA", "MDS-RS", "MDS-RS-SLD", "Pure Sideroblastic Anemia", "pure sideroblastic anemia", "Pure sideroblastic Anemia", "MDS with ring sideroblasts", "Refractory anemia with sideroblasts", "Myelodysplasia with sideroblastosis", "Refractory anaemia with sideroblasts", "anemia; refractory, with sideroblasts", "refractory; anemia, with sideroblasts", "primary acquired sideroblastic anemia", "refractory Anemia with Ring sideroblasts", "refractory anemia with ring sideroblasts", "Refractory Anemia with Ring Sideroblasts", "Refractory anemia with ring sideroblasts", "acquired idiopathic sideroblastic anemia", "Refractory anemia with ringed sideroblasts", "refractory anemia with ringed sideroblasts", "refractory Anemia with ringed sideroblasts", "Refractory Anemia with Ringed Sideroblasts", "Refractory anaemia with ringed sideroblasts", "Myelodysplastic Syndrome with Ring Sideroblasts", "Myelodysplastic syndrome with ring sideroblasts", "myelodysplastic syndrome with Ring sideroblasts", "myelodysplastic syndrome with ring sideroblasts", "RARS - Refractory anemia with ringed sideroblasts", "Refractory anemia with ringed sideroblasts (RARS)", "RARS - Refractory anaemia with ringed sideroblasts", "refractory anemia with ring sideroblasts (diagnosis)", "MDS-RS - myelodysplastic syndrome with ring sideroblasts", "Myelodysplastic syndrome with ring sideroblasts and single lineage dysplasia", "Myelodysplastic Syndrome with Ring Sideroblasts and Single Lineage Dysplasia", "Refractory anemia with ring sideroblasts associated with marked thrombocytosis", "Refractory anaemia with ring sideroblasts associated with marked thrombocytosis", "Refractory anemia with ringed sideroblasts associated with marked thrombocytosis", "Refractory anaemia with ringed sideroblasts associated with marked thrombocytosis", "Myelodysplastic syndrome with ring sideroblasts and single lineage dysplasia (disorder)", "Myelodysplastic syndrome with ring sideroblasts and single lineage dysplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myelodysplastic syndrome with ring sideroblasts", "shortest_name_length": 4}
{"curie": "UMLS:C0334630", "names": ["Grade 2 Nodular Sclerosis Hodgkin Lymphoma", "Hodgkin lymphoma, nodular sclerosis, grade 2", "Grade 2 Nodular Sclerosis Hodgkin's Lymphoma", "Grade II Nodular Sclerosis Hodgkin's Lymphoma", "Grade 2 Nodular Sclerosis Classic Hodgkin Lymphoma", "Grade 2 Nodular Sclerosis Classical Hodgkin Lymphoma", "Classical Hodgkin lymphoma, nodular sclerosis, grade 2", "Hodgkin's disease, nodular sclerosis, syncytial variant", "Hodgkin's disease, nodular sclerosis, lymphocyte depletion", "Hodgkin's disease, nodular sclerosis, lymphocytic depletion", "Hodgkin lymphoma, nodular sclerosis, grade 2 (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade 2 Nodular Sclerosis Classic Hodgkin Lymphoma", "shortest_name_length": 42}
{"curie": "UMLS:C1332525", "names": ["Benign Ovarian Seromucinous Tumor", "Benign Seromucinous Cystadenoma/Adenofibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Ovarian Seromucinous Tumor", "shortest_name_length": 33}
{"curie": "UMLS:C0205642", "names": ["Oncocytic carcinoma", "Oncocytic Carcinoma", "carcinoma oncocytic", "ONCOCYTOMA, MALIGNANT", "hurthle cell carcinoma", "Hurthle cell carcinoma", "Hurthle Cell Carcinoma", "Hurthle cell; carcinoma", "Huerthle cell carcinoma", "carcinoma; Hurthle cell", "Oxyphilic Adenocarcinoma", "oxyphilic adenocarcinoma", "Oncocytic adenocarcinoma", "Oxyphilic adenocarcinoma", "Oncocytic Adenocarcinoma", "Oxyphilic Adenocarcinomas", "Adenocarcinoma, Oxyphilic", "Adenocarcinomas, Oxyphilic", "Hurthle Cell Adenocarcinoma", "Hurthle cell adenocarcinoma", "adenocarcinoma; Hurthle cell", "Hurthle cell; adenocarcinoma", "Oxyphilic adenocarcinoma (disorder)", "oxyphilic adenocarcinoma (diagnosis)", "Follicular carcinoma, oxyphilic cell", "Oxyphilic adenocarcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma, Oxyphilic", "shortest_name_length": 19}
{"curie": "MONDO:0007257", "names": ["Cmct", "CMCT", "CANDF1", "candidiasis, familial, 1", "CANDIDIASIS, FAMILIAL, 1", "Candidiasis, Familial, 1", "candidiasis, familial, 1, autosomal dominant", "CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL DOMINANT, WITH OR WITHOUT THYROID DISEASE", "Candidiasis, Familial Chronic Mucocutaneous, Autosomal Dominant, With Or Without Thyroid Disease", "candidiasis, familial chronic mucocutaneous, autosomal dominant, with or without thyroid disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "candidiasis, familial, 1", "shortest_name_length": 4}
{"curie": "UMLS:C5239401", "names": ["Myelodysplastic Syndrome with Point Mutations", "Myelodysplastic Syndrome with Somatic Mutations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myelodysplastic Syndrome with Somatic Mutations", "shortest_name_length": 45}
{"curie": "MONDO:0006737", "names": ["Dystocia", "dystocia", "dystocias", "Dystocias", "Dystocia NOS", "Labor problem", "Dystocia, NOS", "abnormal labor", "Abnormal labor", "LABOR ABNORMAL", "ABNORMAL LABOR", "Labor abnormal", "Labor Dystocia", "Labour problem", "Difficult labor", "Labour abnormal", "abnormal; labor", "difficult labor", "Abnormal labour", "labour problems", "Labor, abnormal", "Delivery problem", "delivery problem", "Difficult labour", "LABOR DIFFICULTY", "delivery problems", "dysfunctional labor", "Failure to Progress", "Dysfunctional Labor", "Dysfunctional labor", "Abnormal labor, NOS", "Labor, dysfunctional", "Dysfunctional labour", "Arrest of Dilatation", "Abnormal labour, NOS", "Labor problem (finding)", "Delivery problem (finding)", "dysfunctional labor was observed", "Unspecified abnormality of labor", "Unspecified abnormality of labour", "dysfunctional labor (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dystocia", "shortest_name_length": 8}
{"curie": "MONDO:0009780", "names": ["Czeizel syndrome", "Lethal omphalocele-cleft palate syndrome", "lethal omphalocele-cleft palate syndrome", "Omphalocele cleft palate syndrome lethal", "omphalocele cleft palate syndrome lethal", "cleft palate-omphalocele syndrome, lethal", "Omphalocele-Cleft Palate Syndrome, Lethal", "Cleft palate-omphalocele syndrome, lethal", "CLEFT PALATE-OMPHALOCELE SYNDROME, LETHAL", "OMPHALOCELE-CLEFT PALATE SYNDROME, LETHAL", "omphalocele-cleft palate syndrome, lethal", "Lethal omphalocele with cleft palate syndrome", "Lethal omphalocele with cleft palate syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal omphalocele-cleft palate syndrome", "shortest_name_length": 16}
{"curie": "UMLS:C4682623", "names": ["Ovarian Cancer by AJCC v8 Stage", "Ovarian Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Cancer by AJCC v8 Stage", "shortest_name_length": 31}
{"curie": "UMLS:C0877550", "names": ["Carcinomatous ascites", "Carcinomatous Ascites"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carcinomatous ascites", "shortest_name_length": 21}
{"curie": "UMLS:C1333861", "names": ["Moderate Glandular Dysplasia", "Grade 2 Glandular Intraepithelial Neoplasia", "Grade II Glandular Intraepithelial Neoplasia", "Glandular intraepithelial neoplasia, grade II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade II Glandular Intraepithelial Neoplasia", "shortest_name_length": 28}
{"curie": "MONDO:0021124", "names": ["Infertility;F", "Subfertility;F", "female sterility", "sterility, female", "female infertility", "Infertility female", "FEMALE INFERTILITY", "Female infertility", "Female Infertility", "infertility female", "female subfertility", "Female Subfertility", "females infertility", "infertility; female", "Infertility, female", "Female subfertility", "Infertility, Female", "female sub-fertility", "Subfertility, Female", "postpartum sterility", "Female Sub-Fertility", "subfertility, female", "Sub-Fertility, Female", "Sub Fertility, Female", "sub fertility, female", "sub-fertility, female", "Subfertility (female)", "sterility, postpartum", "Female infertility, NOS", "FEMALE INFERTILITY DISORDERS", "Female infertility (disorder)", "female infertility (diagnosis)", "Female infertility, unspecified", "female reproductive system infertility", "Infertility, female, of unspecified origin", "female reproductive system infertility disorder", "infertility disorder of female reproductive system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "female infertility", "shortest_name_length": 13}
{"curie": "UMLS:C0854693", "names": ["Anesthetic complication neurological", "Anaesthetic complication neurological"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anesthetic complication neurological", "shortest_name_length": 36}
{"curie": "UMLS:C5206770", "names": ["Refractory Epithelioid Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Epithelioid Sarcoma", "shortest_name_length": 30}
{"curie": "MONDO:0011937", "names": ["PSS4", "peeling skin syndrome 4", "PEELING SKIN SYNDROME 4", "CSTA peeling skin syndrome", "peeling skin syndrome type 4", "ichthyosis bullosa of Siemens-like", "ichthyosis, exfoliative, autosomal recessive", "peeling skin syndrome caused by mutation in CSTA", "Exfoliative Ichthyosis, Autosomal Recessive, IBS-Like", "Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa of Siemens-like"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peeling skin syndrome 4", "shortest_name_length": 4}
{"curie": "UMLS:C0392445", "names": ["Urbach-Oppenheim", "Oppenheim-Urbach", "Appenheim's disease", "necrobiosis diabeticorum", "Oppenheim-Urbach disease", "OPPENHEIM-URBACH DISEASE", "Necrobiosis diabeticorum", "diabetic necrobiosis lipoidica", "Diabetic necrobiosis lipoidica", "necrobiosis lipoidica diabetic", "Necrobiosis lipoidica diabetic", "Necrobiosis lipoidica diabeticorum", "NECROBIOSIS LIPOIDICA DIABETICORUM", "Necrobiosis Lipoidica Diabeticorum", "necrobiosis lipoidica diabeticorum", "Diabeticorum, Necrobiosis Lipoidica", "NLD - Necrobiosis lipoidica diabeticorum", "Necrobiosis lipoidica diabeticorum (disorder)", "necrobiosis lipoidica diabeticorum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Necrobiosis Lipoidica Diabeticorum", "shortest_name_length": 16}
{"curie": "UMLS:C5554887", "names": ["MYOD1-Mutant Spindle Cell/Sclerosing Rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MYOD1-Mutant Spindle Cell/Sclerosing Rhabdomyosarcoma", "shortest_name_length": 53}
{"curie": "MONDO:0010688", "names": ["hereditary sensory neuropathy X-linked", "neuropathy, hereditary sensory, X-linked", "NEUROPATHY, HEREDITARY SENSORY, X-LINKED", "Neuropathy, Hereditary Sensory, X-Linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary sensory neuropathy X-linked", "shortest_name_length": 38}
{"curie": "UMLS:C0919603", "names": ["Application site urticaria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Application site urticaria", "shortest_name_length": 26}
{"curie": "UMLS:C3273032", "names": ["Lymphocyte-Rich Hepatocellular Carcinoma", "Lymphoepithelioma-Like Hepatocellular Cancer", "Lymphoepithelioma-Like Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphocyte-Rich Hepatocellular Carcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0009656", "names": ["MPS3B", "MPS 3B", "MPSIIIB", "MPS 3 B", "MPS IIIB", "MPS III B", "Sanfilippo", "Sanfilippo B", "NAGLU DEFICIENCY", "NAGLU deficiency", "NAGLU Deficiency", "Deficiency, NAGLU", "NAGLU Deficiencies", "Deficiencies, NAGLU", "SANFILIPPO SYNDROME B", "Sanfilippo syndrome B", "Sanfilippo Syndrome B", "Sanfilippo B syndrome", "type B Sanfilippo syndrome", "Sanfilippo syndrome type B", "Sanfilippo syndrome, type B", "Mucopolysaccharidosis III-B", "Mucopolysaccharidosis type 3B", "mucopolysaccharidosis type 3B", "Mucopoly-saccharidosis type 3B", "mucopolysaccharidosis, type 3B", "Mucopolysaccharidosis Type 3 B", "Mucopolysaccharidosis Type IIIB", "mucopolysaccharidosis type IIIB", "Mucopolysaccharidosis type IIIB", "mucopolysaccharidosis type III-B", "Mucopolysaccharidosis, type IIIB", "Mucopolysaccharidosis, MPS-III-B", "Mucopolysaccharidosis Type IIIBs", "mucopolysaccharidosis, type IIIB", "MUCOPOLYSACCHARIDOSIS, TYPE IIIB", "Mucopolysaccharidosis III-B (disorder)", "MPS III-B - Mucopolysaccharidosis III-B", "Alpha-N-acetylglucosaminidase deficiency", "alpha-N-acetylglucosaminidase deficiency", "MPSIIIB - Mucopolysaccharidosis type IIIB", "N-acetyl-alpha-glucosaminidase deficiency", "N-Acetyl-alpha-D-glucosaminidase deficiency", "N-Acetyl-alpha-D-Glucosaminidase Deficiency", "N-ACETYL-ALPHA-D-GLUCOSAMINIDASE DEFICIENCY", "N Acetyl alpha D Glucosaminidase Deficiency", "N-Acetyl-Alpha-D-glucosaminidase deficiency", "Deficiency, N-Acetyl-alpha-D-Glucosaminidase", "mucopolysaccharidosis type III-B (diagnosis)", "N-Acetyl-alpha-D-Glucosaminidase Deficiencies", "mucopolysaccharidosis type IIIB (Sanfilippo B)", "Deficiencies, N-Acetyl-alpha-D-Glucosaminidase"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucopolysaccharidosis type 3B", "shortest_name_length": 5}
{"curie": "UMLS:C0029231", "names": ["Organic Mental Disorders, Substance-Induced", "Organic Mental Disorders, Substance Induced"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Organic Mental Disorders, Substance-Induced", "shortest_name_length": 43}
{"curie": "MONDO:0012027", "names": ["AIS2", "VAMAS3", "autoimmune disease, susceptibility to, 2", "AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 2", "AUTOIMMUNE DISEASE SUSCEPTIBILITY LOCUS, CHROMOSOME 7-RELATED", "autoimmune disease susceptibility locus, chromosome 7-related", "vitiligo-associated multiple autoimmune disease susceptibility 3", "VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune disease, susceptibility to, 2", "shortest_name_length": 4}
{"curie": "MONDO:0005323", "names": ["bacterial venereal disease", "venereal disease bacterial", "Bacterial Venereal Disease", "Bacterial Venereal Diseases", "Venereal Disease, Bacterial", "Disease, Bacterial Venereal", "Venereal Diseases, Bacterial", "sexually transmitted disease bacterial", "sexually transmitted bacterial disease", "Bacterial Sexually Transmitted Disease", "bacterial sexually transmitted disease", "Sexually Transmitted Disease, Bacterial", "Bacterial Sexually Transmitted Diseases", "Sexually Transmitted Diseases, Bacterial", "sexually transmitted bacterial disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bacterial sexually transmitted disease", "shortest_name_length": 26}
{"curie": "MONDO:0014835", "names": ["ADSD2", "striatal degeneration, autosomal dominant", "striatal degeneration, autosomal dominant 2", "STRIATAL DEGENERATION, AUTOSOMAL DOMINANT 2", "striatal Degeneration, autosomal dominant 2", "striatal Degeneration, autosomal dominant type 2", "PDE10A striatal degeneration, autosomal dominant", "striatal degeneration, autosomal dominant 2; ADSD2", "striatal degeneration, autosomal dominant caused by mutation in PDE10A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "striatal degeneration, autosomal dominant 2", "shortest_name_length": 5}
{"curie": "MONDO:0043762", "names": ["pregnancy tubal", "Pregnancy;tubal", "Tubal Pregnancy", "Tubal pregnancy", "tubal pregnancy", "Pregnancy, tubal", "tubal; pregnancy", "PREGNANCY, TUBAL", "Pregnancy, Tubal", "tubal Pregnancies", "Tubal Pregnancies", "tubal pregnancies", "Pregnancies, Tubal", "Pregnancies, tubal", "fallopian pregnancy", "pregnancy fallopian", "Fallopian pregnancy", "Tubal pregnancy NOS", "tubal ectopic pregnancy", "ECTOPIC PREGNANCY TUBAL", "ectopic pregnancy tubal", "TUBAL ECTOPIC PREGNANCY", "fallopian tube pregnancy", "Fallopian tube pregnancy", "FALLOPIAN TUBE PREGNANCY", "fallopian pregnancy tube", "fallopian pregnancies tube", "Tubal pregnancy (disorder)", "tubal pregnancy (diagnosis)", "fallopian tube ectopic pregnancy", "ectopic pregnancy of fallopian tube"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tubal pregnancy", "shortest_name_length": 15}
{"curie": "MONDO:0005659", "names": ["Ozena", "ozena", "OZENA", "ozaena", "Ozaena", "Ozenas", "dry rhinitis", "rhinitis sicca", "Ozena (disorder)", "Atrophic Rhinitis", "Atrophic rhinitis", "RHINITIS ATROPHIC", "Rhinitis atrophic", "ATROPHIC RHINITIS", "atrophic rhinitis", "ozena (diagnosis)", "rhinitis atrophic", "rhinitis; atrophic", "Rhinitis, Atrophic", "Rhinitis, atrophic", "RHINITIS, ATROPHIC", "rhinitis, atrophic", "atrophic; rhinitis", "Atrophic Rhinitides", "Rhinitides, Atrophic", "Severe chronic rhinitis", "Primary atrophic rhinitis", "Atrophic rhinitis (chronic)", "Atrophic rhinitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrophic rhinitis", "shortest_name_length": 5}
{"curie": "UMLS:C0160447", "names": ["Injury to Peritoneum without mention of Open Wound into Cavity", "Injury to peritoneum without mention of open wound into cavity", "Injury to other intra-abdominal organs without mention of open wound into cavity, peritoneum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury to peritoneum without mention of open wound into cavity", "shortest_name_length": 62}
{"curie": "UMLS:C4526608", "names": ["Stage II Thymoma", "Stage II Thymoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Thymoma AJCC v8", "shortest_name_length": 16}
{"curie": "UMLS:C0270830", "names": ["Somatosensory Seizure", "Somatosensory seizure", "Somatosensory attacks", "Somatosensory Seizures", "Seizure, Somatosensory", "Seizures, Somatosensory", "Seizure(s) Somatosensory", "Seizure, somatosensory, partial", "Somatosensory seizure (disorder)", "Simple partial seizures with somatosensory symptoms", "Simple partial seizure with somatosensory or special sensory dysfunction", "Simple partial seizure with somatosensory or special sensory dysfunction (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Simple partial seizure with somatosensory or special sensory dysfunction", "shortest_name_length": 21}
{"curie": "MONDO:0800155", "names": ["inborn disorder of glycine and serine metabolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of glycine and serine metabolism", "shortest_name_length": 48}
{"curie": "UMLS:C0268889", "names": ["prostatic obstruction", "Prostatic obstruction", "obstruction prostatic", "Obstruction;prostatic", "Prostatic Obstruction", "Prostatic obstruction NOS", "Prostatic obstruction, NOS", "Prostatic obstruction (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostatic Obstruction", "shortest_name_length": 21}
{"curie": "MONDO:0019796", "names": ["ACS", "Apert syndrome", "acrocephalosyndactyly", "Acrocephalosyndactyly", "acrocephalosyndactylia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acrocephalosyndactyly", "shortest_name_length": 3}
{"curie": "MONDO:0010311", "names": ["BMD", "Becker", "Becker dystrophy", "Becker's disease", "becker dystrophy", "beckers dystrophy", "dystrophy; Becker", "Becker; dystrophy", "Becker dystrophinopathy", "dystrophy; Becker's type", "Becker Muscular Dystrophy", "Becker muscular dystrophy", "BECKER MUSCULAR DYSTROPHY", "MUSCULAR DYSTROPHY BECKER", "becker dystrophy muscular", "becker muscular dystrophy", "benign congenital myopathy", "congenital myopathy benign", "Muscular Dystrophy, Becker", "Benign congenital myopathy", "beckers dystrophy muscular", "becker's dystrophy muscular", "becker dystrophies muscular", "Becker's muscular dystrophy", "becker's muscular dystrophy", "Becker's Muscular Dystrophy", "Muscular Dystrophy, Becker's", "MUSCULAR DYSTROPHY, BECKER TYPE", "BMD - Becker muscular dystrophy", "muscular dystrophy, Becker type", "Muscular Dystrophy, Becker Type", "Becker muscular dystrophy (BMD)", "Becker-Kiener muscular dystrophy", "Duchenne/Becker muscular dystrophy", "Becker muscular dystrophy (disorder)", "Benign congenital myopathy (disorder)", "Becker muscular dystrophy (diagnosis)", "benign congenital myopathy (diagnosis)", "progressive muscular dystrophy, Becker type", "muscular; dystrophy, benign (Becker's type)", "dystrophy; muscular, benign (Becker's type)", "Duchenne/Becker muscular dystrophy (DMD/BMD)", "Benign pseudohypertrophic muscular dystrophy", "Becker pseudohypertrophic muscular dystrophy", "Benign Pseudohypertrophic Muscular Dystrophy", "benign pseudohypertrophic muscular dystrophy", "Becker muscular dystrophy, X-linked recessive", "Pseudohypertrophic muscular dystrophy, Becker's type", "muscular dystrophy pseudohypertrophic progressive, Becker type", "Muscular Dystrophy Pseudohypertrophic Progressive, Becker Type", "Muscular Dystrophy, Pseudohypertrophic Progressive, Becker Type", "muscular dystrophy, pseudohypertrophic progressive, Becker type", "MUSCULAR DYSTROPHY, PSEUDOHYPERTROPHIC PROGRESSIVE, BECKER TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Becker muscular dystrophy", "shortest_name_length": 3}
{"curie": "MONDO:0011115", "names": ["SPASTIC PARAPLEGIA AND EVANS SYNDROME", "Spastic Paraplegia And Evans Syndrome", "spastic paraplegia and Evans syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic paraplegia and Evans syndrome", "shortest_name_length": 37}
{"curie": "MONDO:0035740", "names": ["aFXI", "Acquired Factor XI Deficiency", "acquired factor XI deficiency", "Acquired factor XI deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired factor XI deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0054636", "names": ["SKDEAS", "Skraban-Deardorff syndrome", "SKRABAN-DEARDORFF SYNDROME", "Skraban Deardorff syndrome", "Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome", "Intellectual disability, seizures, abnormal gait, facial dysmorphism syndrome", "intellectual disability with seizures, abnormal Gait, and distinctive Facial features", "INTELLECTUAL DISABILITY WITH SEIZURES, ABNORMAL GAIT, AND DISTINCTIVE FACIAL FEATURES", "Intellectual disability, seizures, abnormal gait, facial dysmorphism syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skraban-Deardorff syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C5236143", "names": ["NF1-Associated Malignant Peripheral Nerve Sheath Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "NF1-Associated Malignant Peripheral Nerve Sheath Tumor", "shortest_name_length": 54}
{"curie": "MONDO:0014690", "names": ["DKCB7", "DKCA6", "autosomal dominant dyskeratosis congenita 6", "DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 6", "Dyskeratosis Congenita, Autosomal Dominant 6", "dyskeratosis congenita, autosomal dominant 6", "Dyskeratosis Congenita, Autosomal Recessive 7", "dyskeratosis congenita, autosomal recessive 7", "DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 7", "dyskeratosis congenita, autosomal dominant type 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyskeratosis congenita, autosomal dominant 6", "shortest_name_length": 5}
{"curie": "UMLS:C0280399", "names": ["larynx squamous cell carcinoma, stage IV", "Laryngeal squamous cell carcinoma stage IV", "larynx squamous cell carcinoma, metastatic", "laryngeal squamous cell carcinoma, stage IV", "epidermoid carcinoma of the larynx, stage IV", "Metastatic Laryngeal Squamous Cell Carcinoma", "Laryngeal squamous cell carcinoma metastatic", "laryngeal squamous cell carcinoma, metastatic", "epidermoid carcinoma of the larynx, metastatic", "stage IV squamous cell carcinoma of the larynx", "squamous cell carcinoma of the larynx, stage IV", "metastatic squamous cell carcinoma of the larynx", "Metastatic Squamous Cell Carcinoma of the Larynx", "Metastatic Laryngeal Throat Squamous Cell Cancer", "squamous cell carcinoma of the larynx, metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Squamous Cell Carcinoma of the Larynx", "shortest_name_length": 40}
{"curie": "MONDO:0020332", "names": ["SMAHN", "SM-AHN", "SM-AHNMD", "Systemic mastocytosis with AHNMD", "systemic mastocytosis with associated hematologic neoplasm", "Systemic mastocytosis with associated hematologic neoplasm", "systemic mastocytosis with an associated hematological neoplasm", "Systemic Mastocytosis with an Associated Hematological Neoplasm", "systemic mastocytosis with an associated hematological neoplasm (SM-AHN)", "Systemic Mastocytosis with an Associated Hematological Neoplasm (SM-AHN)", "Systemic mastocytosis with associated hematological clonal non-mast cell disorder", "Systemic mastocytosis with associated haematological clonal non-mast cell disorder", "systemic mastocytosis with associated clonal hematologic non-mast cell lineage disease", "Systemic mastocytosis with associated clonal, hematologic non-mast-cell lineage disease", "systemic mastocytosis with associated clonal, hematologic non-mast-cell lineage disease", "Systemic Mastocytosis with Associated Clonal Hematological non-Mast-Cell Lineage Disease", "systemic mastocytosis with associated clonal hematological non-mast-cell lineage disease", "Systemic mastocytosis with associated clonal, haematologic non-mast-cell lineage disease", "Systemic mastocytosis with associated clonal hematological non-mast cell lineage disease", "systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease", "systemic mastocytosis with associated clonal haematological non-mast cell lineage disease", "Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease", "Systemic mastocytosis with associated clonal haematological non-mast cell lineage disease", "systemic mastocytosis with associated clonal hematologic non-mast cell lineage disease (diagnosis)", "Systemic mastocytosis with associated clonal hematological non-mast cell lineage disease (disorder)", "Systemic mastocytosis with associated clonal, hematologic non-mast-cell lineage disease (morphologic abnormality)", "systemic mastocytosis with associated clonal, hematologic non-mast-cell lineage disease (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease", "shortest_name_length": 5}
{"curie": "UMLS:C1518719", "names": ["Ovarian Leydig Cell Tumor, Non-Hilar Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Leydig Cell Tumor, Non-Hilar Type", "shortest_name_length": 41}
{"curie": "MONDO:0033668", "names": ["DFNA79", "DEAFNESS, AUTOSOMAL DOMINANT 79", "deafness, autosomal dominant 79", "hearing loss, autosomal dominant 79", "autosomal dominant nonsyndromic deafness 79"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal dominant 79", "shortest_name_length": 6}
{"curie": "UMLS:C0694549", "names": ["Community-acquired Pneumonia", "Community-acquired pneumonia", "community acquired pneumonia", "acquired community pneumonia", "Community-Acquired Pneumonia", "community-acquired pneumonia", "Community acquired pneumonia", "PNEUMONIA COMMUNITY ACQUIRED", "CAP - community acquired pneumonia", "Community acquired pneumonia (disorder)", "community-acquired pneumonia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Community acquired pneumonia", "shortest_name_length": 28}
{"curie": "MONDO:0016199", "names": ["qualitative or quantitative defects of protein SERCA1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of protein SERCA1", "shortest_name_length": 53}
{"curie": "MONDO:0015625", "names": ["diazoxide-resistant diffuse hyperinsulinism", "hyperinsulinemic hypoglycemia, diazoxide-resistant diffuse form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diazoxide-resistant diffuse hyperinsulinism", "shortest_name_length": 43}
{"curie": "MONDO:0012265", "names": ["PEE3", "PREECLAMPSIA/eclampsia 3", "preeclampsia/eclampsia 3", "Preeclampsia Eclampsia 3", "PREECLAMPSIA/ECLAMPSIA 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "preeclampsia/eclampsia 3", "shortest_name_length": 4}
{"curie": "MONDO:0014089", "names": ["MSPC", "CIDED", "CIDED, FORMERLY", "PALMOPLANTAR CARCINOMA, MULTIPLE SELF-HEALING", "palmoplantar carcinoma, multiple self-healing", "palmoplantar carcinoma, multiple self-healing; MSPC", "corneal intraepithelial dyskeratosis and ectodermal dysplasia", "corneal intraepithelial dyskeratosis and ectodermal dysplasia, formerly", "CORNEAL INTRAEPITHELIAL DYSKERATOSIS AND ECTODERMAL DYSPLASIA, FORMERLY", "corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0043179", "names": ["piepkorn karp hickok syndrome", "Piepkorn Karp Hickok syndrome", "short ribs, polysyndactyly, cranial synostosis, cleft palate cardiovascular and urogenital anomalies and severe ossification defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "piepkorn karp hickok syndrome", "shortest_name_length": 29}
{"curie": "MONDO:0030506", "names": ["ODG9", "ovarian dysgenesis 9", "OVARIAN DYSGENESIS 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian dysgenesis 9", "shortest_name_length": 4}
{"curie": "MONDO:0003155", "names": ["cavernoma", "Cavernoma", "cavernous nevus", "Cavernous nevus", "cavernous; nevus", "Cavernous naevus", "Naevus;cavernous", "cavernous naevus", "nevus; cavernous", "Cavernous Angioma", "cavernous angioma", "angioma cavernous", "Cavernous angioma", "HEMANGIOMA, MATURE", "Angioma, Cavernous", "angiomas cavernous", "cavernous angiomas", "cavernous hemangioma", "Cavernous Hemangioma", "Cavernous hemangioma", "hemangioma cavernous", "Hemangioma cavernous", "Strawberry Hemangioma", "Haemangioma cavernous", "Cavernous haemangioma", "cavernous hemangiomas", "HEMANGIOMA, CAVERNOUS", "Hemangioma, Cavernous", "Strawberry hemangioma", "Cavernous Hemangiomas", "hemangioma; cavernous", "cavernous haemangioma", "cavernous; hemangioma", "Hemangiomas, Cavernous", "Strawberry Hemangiomas", "Strawberry haemangioma", "Hemangioma, Strawberry", "hemangioma; strawberry", "strawberry; hemangioma", "Cavernous nevus of skin", "Hemangiomas, Strawberry", "[M]Cavernous hemangioma", "[M]Cavernous haemangioma", "Cavernous naevus of skin", "Cavernous angioma of skin", "Cavernous hemangioma (disorder)", "cavernous hemangioma (diagnosis)", "cavernous hemangioma (physical finding)", "cavernous hemangioma (morphologic abnormality)", "Cavernous hemangioma (morphologic abnormality)", "Collection of dilated blood vessels that forms mass"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cavernous hemangioma", "shortest_name_length": 9}
{"curie": "MONDO:0024614", "names": ["DEPRESSION NEUROTIC", "depressive neurosis", "Neurotic depression", "neurotic depression", "Neurotic Depression", "Depression neurotic", "depression; neurotic", "neurotic; depression", "Neurotic Depressions", "Depression, Neurotic", "Depressions, Neurotic", "neurotic depressive state", "Neurotic depressive state", "state; depressive, neurotic", "depressive; state, neurotic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurotic depression", "shortest_name_length": 19}
{"curie": "UMLS:C0334236", "names": ["Polygonal Cell Carcinoma", "polygonal cell carcinoma", "Polygonal cell carcinoma", "polygonal cell carcinoma (diagnosis)", "Polygonal cell carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Polygonal cell carcinoma", "shortest_name_length": 24}
{"curie": "MONDO:0015111", "names": ["gastroesophageal disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastroesophageal disease", "shortest_name_length": 24}
{"curie": "MONDO:0014274", "names": ["LFTD", "L-FERRITIN DEFICIENCY", "L-ferritin deficiency", "LFTD - L-ferritin deficiency", "L-ferritin deficiency (disorder)", "L-ferritin deficiency, dominant and recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "L-ferritin deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0015926", "names": ["PNEUMOCONIOSES", "PNEUMOCONIOSIS", "Pneumoconioses", "pneumoconiosis", "Pneumoconiosis", "pneumoconioses", "Pneumoconiosis NOS", "Black lung disease", "PK - Pneumoconiosis", "Pneumoconiosis, NOS", "Pneumoconiosis (disorder)", "pneumoconiosis (diagnosis)", "Unspecified pneumoconiosis", "Pneumoconiosis, unspecified", "coal worker's pneumoconiosis", "lung; fibrosis, with pneumoconiosis", "fibrosis; lung, with pneumoconiosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pneumoconiosis", "shortest_name_length": 14}
{"curie": "MONDO:0006202", "names": ["Adenosquamous Bile Duct Carcinoma", "bile duct adenosquamous carcinoma", "adenosquamous bile duct carcinoma", "Bile Duct Adenosquamous Carcinoma", "Adenosquamous Carcinoma of Bile Duct", "adenosquamous carcinoma of bile duct", "Adenosquamous Carcinoma of the Bile Duct", "adenosquamous carcinoma of the bile duct", "Extrahepatic Bile Duct Adenosquamous Carcinoma", "extrahepatic bile duct adenosquamous carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extrahepatic bile duct adenosquamous carcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C4330613", "names": ["Burkitt-Like Lymphoma with 11q Aberration", "Burkitt-like lymphoma with 11q aberration", "Large B-Cell Lymphoma with 11q Aberration", "B-Cell Lymphoma with 11q Aberration Resembling Burkitt Lymphoma", "Burkitt-like lymphoma with 11q aberration (morphologic abnormality)", "MYC-Negative B-Cell Lymphoma with 11q Aberration Resembling Burkitt Lymphoma", "MYC-Negative High-Grade B-Cell Lymphoma with 11q Aberration Resembling Burkitt Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Burkitt-like lymphoma with 11q aberration", "shortest_name_length": 41}
{"curie": "UMLS:C3838669", "names": ["Simple Virilizing 21-OHD", "Simple Virilizing 21-Hydroxylase Deficiency", "21-hydroxylase deficiency - simple virilizing", "21-hydroxylase deficiency - simple virilizing (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "21-hydroxylase deficiency - simple virilizing", "shortest_name_length": 24}
{"curie": "MONDO:0004315", "names": ["CLC", "Cholangiolocellular Carcinoma", "cholangiolocellular carcinoma", "intralobular bile duct cholangiocarcinoma", "cholangiocarcinoma of intralobular bile duct"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholangiolocellular carcinoma", "shortest_name_length": 3}
{"curie": "MONDO:0000335", "names": ["parenchymatous neurosyphilis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parenchymatous neurosyphilis", "shortest_name_length": 28}
{"curie": "MONDO:0001879", "names": ["anal cancer", "cancer anus", "anus cancer", "anal cancers", "cancer of anus", "cancer of the anus", "Neoplasm malig;anus", "malignant anal tumor", "Malignant Anal Tumor", "Malignant Tumor of Anus", "Malignant tumor of anus", "malignant anus neoplasm", "Malignant Anal Neoplasm", "malignant tumor of anus", "malignant anal neoplasm", "Malignant tumour of anus", "Malignant Neoplasm of Anus", "Malignant neoplasm of anus", "malignant neoplasm of anus", "malignant tumor of the anus", "Malignant Tumor of the Anus", "malignant neoplasm of the anus", "Malignant Neoplasm of the Anus", "Malignant tumor of anal margin", "malignant neosplasm of the anus", "Malignant tumour of anal margin", "Malignant tumor of anus (disorder)", "malignant neoplasm of anus (diagnosis)", "Malignant neoplasm of anus, unspecified", "Malignant neoplasm of anus, unspecified site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anus cancer", "shortest_name_length": 11}
{"curie": "MONDO:0012334", "names": ["SPG29", "spastic paraplegia 29", "hereditary spastic paraplegia 29", "hereditary spastic paraplegia type 29", "autosomal dominant spastic paraplegia 29", "SPASTIC PARAPLEGIA 29, AUTOSOMAL DOMINANT", "Spastic paraplegia 29, autosomal dominant", "spastic paraplegia 29, autosomal dominant", "Autosomal dominant spastic paraplegia type 29", "autosomal dominant spastic paraplegia type 29", "familial spastic paraplegia autosomal dominant type 29", "Autosomal dominant spastic paraplegia type 29 (disorder)", "Autosomal dominant spastic paraplegia type 29 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 29", "shortest_name_length": 5}
{"curie": "UMLS:C5669784", "names": ["Familial Catecholamine-Induced QT Prolongation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Familial Catecholamine-Induced QT Prolongation", "shortest_name_length": 46}
{"curie": "MONDO:0017566", "names": ["macrodactyly of foot, unilateral", "macrodactyly of toes, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macrodactyly of toes, unilateral", "shortest_name_length": 32}
{"curie": "UMLS:C1708955", "names": ["Malignant Mediastinal Germ Cell Tumor with Associated Hematologic Malignancy", "Malignant Mediastinal Germ Cell Tumor with Associated Hematological Malignancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Mediastinal Germ Cell Tumor with Associated Hematologic Malignancy", "shortest_name_length": 76}
{"curie": "MONDO:0007852", "names": ["Ppk with Deafness", "Ppk-Deafness Syndrome", "PPK-deafness syndrome", "Keratoderma palmoplantar deafness", "keratoderma palmoplantar deafness", "palmoplantar keratoderma with deafness", "Palmoplantar Keratoderma with Deafness", "keratoderma palmoplantar, with deafness", "Keratoderma palmoplantar, with deafness", "KERATODERMA, PALMOPLANTAR, WITH DEAFNESS", "Keratoderma, Palmoplantar, With Deafness", "keratoderma, palmoplantar, with deafness", "Palmoplantar Keratoderma-Deafness Syndrome", "palmoplantar keratoderma-deafness syndrome", "Palmoplantar keratoderma-deafness syndrome", "palmoplantar hyperkeratosis-deafness syndrome", "Palmoplantar Hyperkeratosis-Deafness Syndrome", "Palmoplantar hyperkeratosis-deafness syndrome", "Diffuse palmoplantar keratoderma with deafness", "palmoplantar keratoderma-hearing loss syndrome", "Palmoplantar keratoderma-hearing loss syndrome", "Palmoplantar Keratoderma-Hearing Loss Syndrome", "Palmoplantar keratoderma with deafness syndrome", "Palmoplantar Hyperkeratosis-Hearing Loss Syndrome", "palmoplantar hyperkeratosis-hearing loss syndrome", "Palmoplantar hyperkeratosis-hearing loss syndrome", "Hereditary palmoplantar keratoderma with deafness", "palmoplantar keratoderma and sensorineural deafness", "Palmoplantar keratoderma and sensorineural deafness", "diffuse palmoplantar keratoderma with deafness (subtype)", "Palmoplantar keratoderma with deafness syndrome (disorder)", "Focal palmoplantar keratoderma with sensorineural deafness", "hereditary palmoplantar keratoderma with deafness (subtype)", "focal palmoplantar keratoderma with sensorineural deafness (subtype)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "palmoplantar keratoderma-deafness syndrome", "shortest_name_length": 17}
{"curie": "UMLS:C0338945", "names": ["somatoform autonomic dysfunction respiratory tract", "Respiratory Malfunction Arising from Mental Factor", "Respiratory malfunction arising from mental factors", "Somatoform autonomic dysfunction, respiratory system", "Somatoform autonomic dysfunction - respiratory tract", "somatoform autonomic dysfunction of respiratory tract", "Somatoform autonomic dysfunction - respiratory tract (disorder)", "somatoform autonomic dysfunction of respiratory tract (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Somatoform autonomic dysfunction - respiratory tract", "shortest_name_length": 50}
{"curie": "UMLS:C0005659", "names": ["sting bite", "Sting/bite", "bite sting", "bites sting", "bites stings", "stings bites", "bites stinging", "Bites and stings", "Bites and Stings", "Stings and Bites"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bites and Stings", "shortest_name_length": 10}
{"curie": "MONDO:0020510", "names": ["idiopathic syringomyelia", "Idiopathic syringomyelia", "Idiopathic syringomyelia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic syringomyelia", "shortest_name_length": 24}
{"curie": "UMLS:C0278688", "names": ["Stage IV Ovarian Carcinoma", "stage IV ovarian carcinoma", "ovarian carcinoma, stage IV", "metastatic ovarian carcinoma", "Metastatic Ovarian Carcinoma", "ovarian carcinoma, metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Ovarian Carcinoma", "shortest_name_length": 26}
{"curie": "UMLS:C4331349", "names": ["StAR Deficiency", "Steroidogenic Acute Regulatory Protein Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Steroidogenic Acute Regulatory Protein Deficiency", "shortest_name_length": 15}
{"curie": "MONDO:0001895", "names": ["Retrobulbar neuritis", "Acute retrobulbar neuritis", "acute retrobulbar neuritis", "retrobulbar neuritis acute", "retrobulbar neuritis, acute", "Retrobulbar neuritis (acute)", "retrobulbar neuritis (acute)", "Acute retrobulbar optic neuritis", "Acute retrobulbar neuritis (disorder)", "Acute retrobulbar neuritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute retrobulbar neuritis", "shortest_name_length": 20}
{"curie": "MONDO:0003497", "names": ["RENAL PELVIS EPIDERMOID CARCINOMA", "Renal Pelvis Epidermoid Carcinoma", "Renal Pelvis Squamous Cell Cancer", "renal pelvis squamous cell cancer", "renal pelvis epidermoid carcinoma", "kidney pelvis epidermoid carcinoma", "Kidney Pelvis Epidermoid Carcinoma", "Epidermoid Carcinoma of Renal Pelvis", "Renal Pelvis Squamous Cell Carcinoma", "renal pelvis squamous cell carcinoma", "epidermoid carcinoma of renal pelvis", "kidney pelvis squamous cell carcinoma", "epidermoid carcinoma of kidney pelvis", "Kidney Pelvis Squamous Cell Carcinoma", "Epidermoid Carcinoma of Kidney Pelvis", "squamous cell carcinoma of renal pelvis", "Squamous Cell Carcinoma of Renal Pelvis", "kidney renal pelvis squamous cell cancer", "KIDNEY, PELVIS, CARCINOMA, SQUAMOUS CELL", "squamous cell carcinoma of kidney pelvis", "Epidermoid Carcinoma of the Renal Pelvis", "Squamous Cell Carcinoma of Kidney Pelvis", "epidermoid carcinoma of the renal pelvis", "epidermoid carcinoma of the kidney pelvis", "RENAL CANCER, PELVIS EPIDERMOID CARCINOMA", "Epidermoid carcinoma of the kidney Pelvis", "Epidermoid Carcinoma of the Kidney Pelvis", "Squamous Cell Carcinoma of the Renal Pelvis", "squamous cell carcinoma of the renal pelvis", "Squamous Cell Carcinoma of the Kidney Pelvis", "squamous cell carcinoma of the kidney pelvis", "squamous cell carcinoma of renal pelvis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal pelvis squamous cell carcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C0274727", "names": ["toxicity digoxin", "Digoxin toxicity", "DIGOXIN TOXICITY", "digoxin toxicity", "Digoxin poisoning", "digoxin poisoning", "digoxin toxicities", "DIGOXIN INTOXICATION", "digoxin intoxication", "Poisoning by digoxin", "toxicity from digoxin", "Poisoning caused by digoxin", "digoxin toxicity (diagnosis)", "Poisoning caused by digoxin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Poisoning by digoxin", "shortest_name_length": 16}
{"curie": "UMLS:C4054281", "names": ["P1 Hydronephrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "P1 Hydronephrosis", "shortest_name_length": 17}
{"curie": "MONDO:0008974", "names": ["hem", "GRBGD", "HEM dysplasia", "hem dysplasia", "Greenberg dysplasia", "GREENBERG DYSPLASIA", "Hem Skeletal Dysplasia", "hem skeletal dysplasia", "HEM SKELETAL DYSPLASIA", "hem/Greenberg dysplasia", "Greenberg Skeletal Dysplasia", "Greenberg skeletal dysplasia", "MOTH-EATEN SKELETAL DYSPLASIA", "moth-eaten skeletal dysplasia", "Moth-Eaten Skeletal Dysplasia", "Greenberg dysplasia (disorder)", "skeletal dysplasia, Greenberg type", "Skeletal dysplasia, Greenberg type", "hydrops-ectopic calcification-motheaten syndrome", "Hydrops-ectopic calcification-motheaten syndrome", "CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE", "Chondrodystrophy, Hydropic And Prenatally Lethal Type", "chondrodystrophy, hydropic and prenatally lethal type", "HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA", "hydrops-ectopic calcification-moth-eaten skeletal dysplasia", "Hydrops-Ectopic Calcification-Moth-Eaten Skeletal Dysplasia", "hydrops, ectopic calcification, moth-eaten skeletal dysplasia", "Hydrops - Ectopic Calcification - Moth-Eaten Skeletal Dysplasia", "autosomal recessive lethal chondrodystrophy with congenital hydrops"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Greenberg dysplasia", "shortest_name_length": 3}
{"curie": "UMLS:C1720894", "names": ["Male Urogenital Disease", "Urogenital Disease, Male", "Male Urogenital Diseases", "Urogenital Diseases, Male", "Male Genitourinary Disease", "Genitourinary Disease, Male", "Male Genitourinary Diseases", "Genitourinary Diseases, Male"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Male Urogenital Diseases", "shortest_name_length": 23}
{"curie": "MONDO:0020636", "names": ["Mendelian susceptibility to mycobacterial diseases due to a complete deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mendelian susceptibility to mycobacterial diseases due to a complete deficiency", "shortest_name_length": 79}
{"curie": "MONDO:0019154", "names": ["TFM", "AIS", "AR deficiency", "AR DEFICIENCY", "DHTR deficiency", "Morris syndrome", "DHTR DEFICIENCY", "testicular feminization", "Feminisation - testicular", "Goldberg-Maxwell syndrome", "Goldberg - Maxwell syndrome", "androgen receptor deficiency", "Androgen Resistance Syndrome", "androgen resistance syndrome", "Androgen resistance syndrome", "ANDROGEN RECEPTOR DEFICIENCY", "Androgen Resistance Syndromes", "syndrome; androgen resistance", "Resistance Syndrome, Androgen", "androgen resistance; syndrome", "Resistance Syndromes, Androgen", "ANDROGEN INSENSITIVITY SYNDROME", "Androgen-Insensitivity Syndrome", "Androgen Insensitivity Syndrome", "androgen insensitivity syndrome", "Androgen insensitivity syndrome", "androgen-insensitivity syndrome", "Androgen Insensitivity Syndromes", "Testicular Feminization Syndrome", "Testicular feminization syndrome", "Insensitivity Syndrome, Androgen", "TESTICULAR FEMINIZATION SYNDROME", "testicular feminization syndrome", "Androgen-Insensitivity Syndromes", "testicular Feminization syndrome", "Androgen resistance syndrome, NOS", "Insensitivity Syndromes, Androgen", "dihydrotestosterone receptor deficiency", "Androgen resistance syndrome (disorder)", "DIHYDROTESTOSTERONE RECEPTOR DEFICIENCY", "androgen insensitivity, X-linked recessive", "androgen insensitivity syndrome (diagnosis)", "testicular feminization syndrome (formerly)", "Androgen insensitivity syndrome, unspecified", "pseudohermaphroditism; male, with androgen resistance", "Male Pseudohermaphroditism Due to Androgen Insensitivity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "androgen insensitivity syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0008765", "names": ["LCA2", "Leber congenital amaurosis 2", "Leber Congenital Amaurosis 2", "LEBER CONGENITAL AMAUROSIS 2", "amaurosis congenita of Leber 2", "amaurosis congenita of Leber II", "AMAUROSIS CONGENITA OF LEBER II", "Amaurosis Congenita Of Leber Ii", "RPE65 Leber congenital amaurosis", "Leber congenital amaurosis type 2", "Amaurosis congenita of Leber, type 2", "amaurosis congenita of Leber, type 2", "LEBER CONGENITAL AMAUROSIS, TYPE II (disorder)", "Leber congenital amaurosis caused by mutation in RPE65"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leber congenital amaurosis 2", "shortest_name_length": 4}
{"curie": "MONDO:0004116", "names": ["Esophageal Small Cell NEC", "esophageal small cell NEC", "Esophagus Oat Cell Carcinoma", "esophagus Oat cell carcinoma", "esophageal Oat cell carcinoma", "Esophageal Oat Cell Carcinoma", "Esophagus Small Cell Carcinoma", "esophagus small cell carcinoma", "Esophageal Small Cell Carcinoma", "esophageal small cell carcinoma", "oesophagus small cell carcinoma", "small cell carcinoma, esophagus", "Oat Cell Carcinoma of Esophagus", "Oat cell carcinoma of esophagus", "Small Cell Carcinoma, Esophagus", "Oat cell carcinoma of oesophagus", "small cell carcinoma of esophagus", "Small Cell Carcinoma of Esophagus", "Small cell carcinoma of esophagus", "Small cell carcinoma of oesophagus", "Oat cell carcinoma of the esophagus", "Oat Cell Carcinoma of the Esophagus", "small cell carcinoma of the esophagus", "Small Cell Carcinoma of the Esophagus", "small cell carcinoma of esophagus (diagnosis)", "esophageal small cell neuroendocrine carcinoma", "Esophageal Small Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophageal small cell neuroendocrine carcinoma", "shortest_name_length": 25}
{"curie": "UMLS:C5204262", "names": ["Central Lung", "Central Lung Parenchyma Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Lung Parenchyma Tumor", "shortest_name_length": 12}
{"curie": "MONDO:0800137", "names": ["early-onset pulmonary and cutaneous vasculitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early-onset pulmonary and cutaneous vasculitis", "shortest_name_length": 46}
{"curie": "MONDO:0007229", "names": ["Short 4th toe", "Short fourth toe", "toe, fourth, short", "Brachymetatarsus 4", "TOE, FOURTH, SHORT", "BRACHYMETATARSUS IV", "metatarsus IV, short", "METATARSUS IV, SHORT", "Brachymetatarsus type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brachymetatarsus 4", "shortest_name_length": 13}
{"curie": "MONDO:0008521", "names": ["TCC", "Tarsal-Carpal Coalition Syndrome", "tarsal carpal coalition syndrome", "Tarsal carpal coalition syndrome", "Tarsal-carpal coalition syndrome", "tarsal-carpal coalition syndrome", "TARSAL-CARPAL COALITION SYNDROME", "NOG-Related-Symphalangism Spectrum Disorder", "Tarsal-carpal coalition syndrome (disorder)", "NOG gene-related symphalangism spectrum disorder", "Synostosis of Talus and Calcaneus with Short Stature", "SYNOSTOSIS OF TALUS AND CALCANEUS WITH SHORT STATURE", "synostosis of talus and calcaneus with short stature"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tarsal-carpal coalition syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0024664", "names": ["pregnancy; hypertension", "Gestational hypertension", "gestational hypertension", "GESTATIONAL HYPERTENSION", "Hypertension gestational", "Gestational Hypertension", "hypertension, gestational", "hypertension in pregnancy", "Hypertension, Gestational", "gestational hypertension NOS", "GH - Gestational hypertension", "Pregnancy-Induced Hypertension", "pregnancy induced hypertension", "PREGNANCY INDUCED HYPERTENSION", "Pregnancy-induced hypertension", "Pregnancy Induced Hypertension", "Pregnancy induced hypertension", "pregnancy-induced hypertension", "induced hypertension, pregnancy", "Induced Hypertension, Pregnancy", "Hypertension, Pregnancy Induced", "hypertension, pregnancy induced", "Hypertension, Pregnancy-Induced", "HYPERTENSION, PREGNANCY-INDUCED", "hypertension, pregnancy-induced", "induced Hypertensions, pregnancy", "hypertensions, pregnancy induced", "pregnancy transient hypertension", "Hypertensions, Pregnancy Induced", "Induced Hypertensions, Pregnancy", "Pregnancy associated hypertension", "Pregnancy Associated Hypertension", "transient hypertension, pregnancy", "hypertension induced by pregnancy", "hypertension, pregnancy transient", "Hypertension induced by pregnancy", "PIH Pregnancy induced hypertension", "hypertension complicating pregnancy", "Hypertensive Disorders of Pregnancy", "Pregnancy-induced hypertension, NOS", "PIH - Pregnancy-induced hypertension", "Gestational hypertension (diagnosis)", "high blood pressure caused by pregnancy", "Pregnancy-induced hypertension (disorder)", "Hypertension-Associated Pregnancy Disorder", "hypertension-associated pregnancy disorder", "hypertension associated disorders of pregnancy", "Hypertension associated disorders of pregnancy", "Hypertension Associated Disorders of Pregnancy", "high blood pressure disorder caused by pregnancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertension, pregnancy-induced", "shortest_name_length": 23}
{"curie": "MONDO:0018931", "names": ["ML3", "ML 3", "MLIII", "ML III", "ML 3 A", "ML IIIA", "Hurler; pseudo", "pseudo; Hurler", "ML 3 Alpha/Beta", "ML 3 alpha/beta", "pseudo-Hurler's", "mucolipidosis 3", "mucolipidosis 3A", "Mucolipidosis III", "ML III ALPHA/BETA", "ML III alpha/beta", "mucolipidosis III", "MUCOLIPIDOSIS III", "MUCOLIPIDOSIS IIIA", "Mucolipidosis IIIa", "psuedo hurler disease", "Pseudo-Hurler disease", "mucolipidosis type 3A", "Psuedo Hurler Disease", "Psuedo-Hurler Disease", "Mucolipidosis Type III", "Type III Mucolipidoses", "mucolipidosis type III", "Type III Mucolipidosis", "Mucolipidosis type III", "Psuedo-Hurler Diseases", "Mucolipidosis, Type III", "Mucolipidosis, type III", "Mucolipidoses, Type III", "Pseudo-Hurler's disease", "pseudo-Hurler's; disease", "mucolipidosis 3 Alpha/Beta", "pseudo-hurler polydystrophy", "Pseudo-Hurler Polydystrophy", "pseudo-Hurler polydystrophy", "Pseudo-Hurler polydystrophy", "PSEUDO-HURLER POLYDYSTROPHY", "Pseudo Hurler Polydystrophy", "MUCOLIPIDOSIS III ALPHA/BETA", "Polydystrophy, Pseudo-Hurler", "Mucolipidosis III Alpha Beta", "mucolipidosis III ALPHA/BETA", "mucolipidosis III alpha/beta", "polydystrophy; pseudo-Hurler's", "Mucolipidosis type 3 alpha/beta", "mucolipidosis type 3 alpha/beta", "Mucolipidosis type III alpha/beta", "mucolipidosis type III alpha/beta", "mucolipidosis type III, alpha/beta", "mucolipidosis 3 Alpha/Beta, atypical", "Mucolipidosis III Alpha Beta, Atypical", "Pseudo-Hurler polydystrophy (disorder)", "MUCOLIPIDOSIS III ALPHA/BETA, ATYPICAL", "disease (or disorder); pseudo-Hurler's"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucolipidosis type III, alpha/beta", "shortest_name_length": 3}
{"curie": "MONDO:0024574", "names": ["VWD", "von Willebrand Disease", "von Willebrand disease", "von Willebrand Disorder", "von Willebrand disorder", "von Willebrand Diseases", "von Willebrand's disease", "von Willebrand's Disease", "von Willebrand disease (hereditary or acquired)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "von Willebrand disease (hereditary or acquired)", "shortest_name_length": 3}
{"curie": "UMLS:C1334433", "names": ["Low Risk Small Intestinal GIST", "Low Risk Small Intestinal Gastrointestinal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Risk Small Intestinal Gastrointestinal Stromal Tumor", "shortest_name_length": 30}
{"curie": "MONDO:0001329", "names": ["accommodative spasm", "ACCOMMODATION SPASM", "Accommodative spasm", "Accommodation spasm", "spasm; accommodation", "accommodation; spasm", "Ciliary muscle spasm", "Spasm of accommodation", "spasm of accommodation", "Spasm of accommodation (disorder)", "spasm of accommodation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "accommodative spasm", "shortest_name_length": 19}
{"curie": "MONDO:0021011", "names": ["BHC", "BCH", "Benign familial chorea", "Benign Hereditary Chorea", "Benign hereditary chorea", "Chorea, Benign Hereditary", "Benign Hereditary Choreas", "Hereditary Chorea, Benign", "chorea, hereditary benign", "chorea, benign hereditary", "CHOREA, BENIGN HEREDITARY", "Hereditary Choreas, Benign", "Choreas, Benign Hereditary", "Benign hereditary chorea (disorder)", "hereditary progressive chorea without dementia", "Hereditary Progressive Chorea Without Dementia", "HEREDITARY PROGRESSIVE CHOREA WITHOUT DEMENTIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary progressive chorea without dementia", "shortest_name_length": 3}
{"curie": "MONDO:0100319", "names": ["MIS-A", "COVID-19–associated multisystem inflammatory syndrome in adults"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "COVID-19–associated multisystem inflammatory syndrome in adults", "shortest_name_length": 5}
{"curie": "MONDO:0005477", "names": ["VT", "vt", "v tach", "ventricular tachycardia", "Tachycardia;ventricular", "Ventricular Tachycardia", "VENTRICULAR TACHYCARDIA", "Tachycardia ventricular", "TACHYCARDIA VENTRICULAR", "Ventricular tachycardia", "Tachycardia, ventricular", "Ventricular Tachycardias", "Tachycardia, Ventricular", "ventricular; tachycardia", "tachycardia; ventricular", "TACHYCARDIA, VENTRICULAR", "Ventricular Tachyarrhythmia", "Ventricular Tachyarrhythmias", "Tachyarrhythmia, Ventricular", "VT - ventricular tachycardia", "VT - Ventricular tachycardia", "Ventricular tachycardia, NOS", "Ventricular tachycardia (Vtach)", "ventricular tachycardia (V-tach)", "Ventricular tachycardia (disorder)", "ventricular tachycardia (diagnosis)", "Ventricular tachycardia, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ventricular tachycardia", "shortest_name_length": 2}
{"curie": "UMLS:C3827678", "names": ["Uterine Carcinosarcoma, Heterologous Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Carcinosarcoma, Heterologous Type", "shortest_name_length": 41}
{"curie": "MONDO:0006358", "names": ["Parotid Squamous Cell Carcinoma", "parotid squamous cell carcinoma", "squamous cell carcinoma of parotid", "Squamous Cell Carcinoma of Parotid", "Parotid Gland Squamous Cell Carcinoma", "parotid gland squamous cell carcinoma", "Squamous Cell Carcinoma of the Parotid", "squamous cell carcinoma of the parotid", "squamous cell carcinoma of parotid gland", "Squamous Cell Carcinoma of Parotid Gland", "squamous cell carcinoma of the parotid gland", "Squamous cell carcinoma of the parotid gland", "Squamous Cell Carcinoma of the Parotid Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parotid gland squamous cell carcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C0948808", "names": ["Catheter blockage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Catheter blockage", "shortest_name_length": 17}
{"curie": "UMLS:C1456786", "names": ["Paranoid state", "PARANOID STATE", "paranoid state", "Paranoid States", "state; paranoid", "paranoid; state", "Paranoid states", "Paranoid state NOS", "Unspecified paranoid state"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paranoid state", "shortest_name_length": 14}
{"curie": "MONDO:0000541", "names": ["Jejunal adenocarcinoma", "jejunal adenocarcinoma", "jejunum adenocarcinoma", "Jejunal Adenocarcinoma", "jejunal adenocarcinoma (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "jejunal adenocarcinoma", "shortest_name_length": 22}
{"curie": "MONDO:0018766", "names": ["CEAS", "chronic enteropathy associated with SLCO2A1 gene"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic enteropathy associated with SLCO2A1 gene", "shortest_name_length": 4}
{"curie": "MONDO:0018011", "names": ["Juvenile overlap myositis", "juvenile overlap myositis", "Juvenile overlap myositis (disorder)", "Juvenile overlap myositis (diagnosis)", "inflammatory myopathy idiopathic juvenile overlap myositis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile overlap myositis", "shortest_name_length": 25}
{"curie": "MONDO:0013203", "names": ["FECD3", "Fcd2 locus", "FCD2 LOCUS", "TCF4 Fuchs' endothelial dystrophy", "Corneal Dystrophy, Fuchs Endothelial, 3", "CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 3", "corneal dystrophy, Fuchs endothelial, 3", "corneal dystrophy, Fuchs endothelial, type 3", "CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, LATE-ONSET", "corneal dystrophy, Fuchs endothelial, late-onset", "Fuchs' endothelial dystrophy caused by mutation in TCF4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal dystrophy, Fuchs endothelial, 3", "shortest_name_length": 5}
{"curie": "MONDO:0019570", "names": ["CSB", "Cockayne syndrome B", "Cockayne syndrome 2", "COCKAYNE SYNDROME B", "Type B Cockayne Syndrome", "Cockayne syndrome type 2", "Cockayne syndrome type B", "Cockayne Syndrome Type B", "Cockayne syndrome type II", "Group B Cockayne Syndrome", "Cockayne Syndrome, Type B", "Type II Cockayne Syndrome", "Cockayne syndrome, type B", "Cockayne Syndrome, Group B", "Cockayne Syndrome, Type II", "Early onset Cockayne syndrome", "Cockayne syndrome type 2 (disorder)", "Cockayne syndrome type B (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cockayne syndrome type 2", "shortest_name_length": 3}
{"curie": "UMLS:C5238508", "names": ["Advanced Epithelioid Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Epithelioid Sarcoma", "shortest_name_length": 28}
{"curie": "MONDO:0001383", "names": ["Malignant myopia", "malignant myopia", "malignant; myopia", "myopia; malignant", "myopia pathological", "Pathological myopia", "pathological myopia", "Degenerative Myopia", "Pathological Myopia", "degenerative myopia", "Degenerative myopia", "Pathological Myopias", "Myopia, Degenerative", "degenerative; myopia", "Myopia, Pathological", "myopia; degenerative", "Degenerative Myopias", "Myopias, Degenerative", "Myopias, Pathological", "Progressive high myopia", "progressive high myopia", "High myopia, progressive", "malignant myopia (diagnosis)", "Degenerative myopia (diagnosis)", "Degenerative progressive high myopia", "Progressive high degenerative myopia", "degenerative progressive high myopia", "progressive high (degenerative) myopia", "Progressive high (degenerative) myopia", "Degenerative progressive high myopia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "degenerative myopia", "shortest_name_length": 16}
{"curie": "UMLS:C4330626", "names": ["Major Salivary Gland Cancer by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Major Salivary Gland Cancer by AJCC v7 Stage", "shortest_name_length": 44}
{"curie": "UMLS:C2939061", "names": ["Intentional medical device removal by patient"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intentional medical device removal by patient", "shortest_name_length": 45}
{"curie": "MONDO:0700039", "names": ["EEC", "BEEC", "Exstrophy-epispadias complex", "Exstrophy epispadias complex", "EEC - exstrophy epispadias complex", "Exstrophy epispadias complex (disorder)", "Bladder Exstrophy and Epispadias Complex", "BLADDER EXSTROPHY AND EPISPADIAS COMPLEX", "Bladder exstrophy-epispadias-cloacal extrophy complex", "bladder exstrophy-epispadias-cloacal extrophy complex", "BEEC - bladder exstrophy, epispadias, cloacal exstrophy complex"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder exstrophy-epispadias-cloacal extrophy complex", "shortest_name_length": 3}
{"curie": "UMLS:C0948815", "names": ["Catheter site erythema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Catheter site erythema", "shortest_name_length": 22}
{"curie": "MONDO:0010069", "names": ["CMn syndrome", "CMN SYNDROME", "CASAMASSIMA-MORTON-NANCE SYNDROME", "Casamassima Morton Nance syndrome", "Casamassima-Morton-Nance syndrome", "Casamassima-Morton-Nance Syndrome", "spondylocostal dysostosis with anal atresia and urogenital anomalies", "SPONDYLOCOSTAL DYSOSTOSIS WITH ANAL ATRESIA AND UROGENITAL ANOMALIES", "Spondylocostal Dysostosis with Anal Atresia and Urogenital Anomalies", "spondylocostal dysostosis-anal and genitourinary malformations syndrome", "spondylocostal dysostosis-anal atresia-genitourinary malformation syndrome", "Spondylocostal dysostosis with anal atresia and genitourinary malformation syndrome", "Spondylocostal dysostosis with anal atresia and genitourinary malformation syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondylocostal dysostosis-anal and genitourinary malformations syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0007396", "names": ["Stanescu osteosclerosis", "dysostosis Stanescu type", "dysostosis, Stanescu type", "Dysostosis, Stanescu type", "OSTEOSCLEROSIS, STANESCU TYPE", "osteosclerosis, Stanescu type", "Osteosclerosis, Stanescu Type", "Osteosclerosis - Stanescu type", "Osteosclerosis - Stanescu type (disorder)", "autosomal dominant osteosclerosis, Stanescu type", "Autosomal dominant osteosclerosis, Stanescu type", "CRANIOFACIAL DYSOSTOSIS WITH DIAPHYSEAL HYPERPLASIA", "Craniofacial Dysostosis with Diaphyseal Hyperplasia", "craniofacial dysostosis with diaphyseal hyperplasia", "craniofacial dysostosis-diaphyseal hyperplasia syndrome", "Craniofacial dysostosis-diaphyseal hyperplasia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dysostosis, Stanescu type", "shortest_name_length": 23}
{"curie": "MONDO:0002275", "names": ["ATHEROSCLEROSIS DIFFUSE", "generalised atherosclerosis", "Generalized Atherosclerosis", "Generalized atherosclerosis", "generalized atherosclerosis", "atherosclerosis generalized", "Generalised atherosclerosis", "ATHEROSCLEROSIS GENERALIZED", "Atherosclerosis generalized", "Atherosclerosis generalised", "Generalized atherosclerosis (disorder)", "generalized atherosclerosis (diagnosis)", "Generalised and unspecified atherosclerosis", "Generalized and unspecified atherosclerosis", "generalized and unspecified atherosclerosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "generalized atherosclerosis", "shortest_name_length": 23}
{"curie": "UMLS:C0086922", "names": ["Rheumatic purpura", "rheumatoid purpura", "purpura rheumatoid", "Rheumatoid Purpura", "Purpura, Rheumatoid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rheumatoid Purpura", "shortest_name_length": 17}
{"curie": "UMLS:C0236036", "names": ["oculomucocutaneous syndrome", "Oculomucocutaneous syndrome", "Muco-cutaneo-ocular syndrome", "muco-cutaneo-ocular syndrome", "Oculo-muco-cutaneous syndrome", "OCULO-MUCO-CUTANEOUS SYNDROME", "Ocular-mucous membrane syndrome", "Stevens-Johnson syndrome with associated ocular and genital lesions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oculomucocutaneous syndrome", "shortest_name_length": 27}
{"curie": "MONDO:0020710", "names": ["Amnionitis", "amnionitis", "Amnionitides", "amnionitides", "Inflammation of amnion", "Amniotic cavity infection", "amniotic cavity infection", "amniotic infection syndrome", "infection of amniotic cavity", "Infection of amniotic cavity", "Amniotic cavity infection NOS", "Inflammation of amnion (disorder)", "Infection of amniotic cavity, NOS", "Infection of amniotic cavity (disorder)", "infection of amniotic cavity (diagnosis)", "Infection of amniotic cavity, unspecified as to episode of care", "Infection of amniotic cavity, unspecified as to episode of care or not applicable"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amnionitis", "shortest_name_length": 10}
{"curie": "MONDO:0045037", "names": ["Hyalohyphomycosis", "hyalohyphomycosis", "Hyalohyphomycoses"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyalohyphomycosis", "shortest_name_length": 17}
{"curie": "UMLS:C5667244", "names": ["Recurrent Nervous System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Nervous System Neoplasm", "shortest_name_length": 33}
{"curie": "MONDO:0007009", "names": ["ureter stone", "stone ureter", "stones ureter", "Ureteric stone", "ureteric stone", "stone ureteral", "Ureteral stone", "ureteral stone", "stone ureteric", "stones ureteric", "ureter calculus", "stones ureteral", "Ureterolithiasis", "ureterolithiasis", "Ureterolithiases", "UERTEROLITHIASIS", "ureteral calculi", "Ureteral calculus", "ureteric calculus", "calculus ureteral", "ureteral calculus", "calculus ureteric", "Ureteric calculus", "calculus of ureter", "Calculus of ureter", "Ureteric stone (disorder)", "calculus of ureter (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ureterolithiasis", "shortest_name_length": 12}
{"curie": "UMLS:C5418795", "names": ["Advanced Vulvar Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Vulvar Carcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0011969", "names": ["CDGIh", "CDG1H", "CDG 1H", "CDG-Ih", "CDG Ih", "ALG8-CDG", "ALG8-CDG (CDG-Ih)", "CDG syndrome type Ih", "Glucosyltransferase 2 deficiency", "glucosyltransferase 2 deficiency", "congenital disorder of glycosylation Ih", "congenital disorder of glycosylation 1h", "ALG8 congenital disorder of glycosylation", "ALG8-congenital disorder of glycosylation", "Congenital disorder of glycosylation type 1h", "congenital disorder of glycosylation type Ih", "Congenital disorder of glycosylation type Ih", "Congenital disorder of glycosylation type 1H", "congenital disorder of glycosylation type 1h", "Congenital Disorder of Glycosylation, Type IH", "congenital disorder of glycosylation, type Ih", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ih", "Carbohydrate deficient glycoprotein syndrome type Ih", "carbohydrate deficient glycoprotein syndrome type Ih", "Asparagine-linked glycosylation 8 congenital disorder of glycosylation", "Asparagine-linked glycosylation 8 congenital disorder of glycosylation (disorder)", "ALG8-CDG - asparagine-linked glycosylation 8 congenital disorder of glycosylation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ALG8-congenital disorder of glycosylation", "shortest_name_length": 5}
{"curie": "MONDO:0020639", "names": ["monosomy", "Monosomy", "monosomies", "Monosomies", "Autosomal deletion", "Autosomal monosomy", "Whole chromosome depletion", "Deletion, whole chromosome", "Monosomy (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "monosomy", "shortest_name_length": 8}
{"curie": "UMLS:C4521616", "names": ["Stage II Bone Cancer", "Stage II Bone Cancer AJCC v8", "Stage II Appendicular Skeleton, Trunk, Skull, and Facial Bones Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Bone Cancer AJCC v8", "shortest_name_length": 20}
{"curie": "MONDO:0013579", "names": ["MMSDHD", "MMSDH deficiency", "MMSDH Deficiency", "MMSDH DEFICIENCY", "developmental delay due to MMSDH deficiency", "developmental delay due to ALDH6A1 deficiency", "methylmalonate semialdehyde dehydrogenase deficiency", "Methylmalonate Semialdehyde Dehydrogenase Deficiency", "METHYLMALONATE SEMIALDEHYDE DEHYDROGENASE DEFICIENCY", "developmental delay due to methylmalonate semialdehyde dehydrogenase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "methylmalonate semialdehyde dehydrogenase deficiency", "shortest_name_length": 6}
{"curie": "MONDO:0005690", "names": ["Caplan syndrome", "caplan syndrome", "CAPLAN SYNDROME", "Caplan Syndrome", "Caplans syndrome", "Caplan's disease", "caplans syndrome", "Caplans Syndrome", "Caplan Syndromes", "Caplan (etiology)", "caplan's syndrome", "Caplan's syndrome", "Caplan's Syndrome", "Caplan (manifestation)", "COLINET-CAPLAN SYNDROME", "Rheumatoid pneumoconiosis", "rheumatoid pneumoconiosis", "PNEUMOCONIOSIS, RHEUMATOID", "Caplan's syndrome (diagnosis)", "Rheumatoid arthritis with pneumoconiosis", "Rheumatoid arthritis-pneumoconiosis syndrome", "Rheumatoid arthritis with pneumoconiosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Caplan syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0024567", "names": ["IHPRF", "Ihprf", "IHPRF1", "HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1", "hypotonia, infantile, with psychomotor retardation and characteristic facies 1", "NALCN hypotonia, infantile, with psychomotor retardation and characteristic facies", "hypotonia, infantile, with psychomotor retardation and characteristic facies caused by mutation in NALCN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotonia, infantile, with psychomotor retardation and characteristic facies 1", "shortest_name_length": 5}
{"curie": "MONDO:0012975", "names": ["DFNA3B", "autosomal dominant deafness 3B", "DEAFNESS, AUTOSOMAL DOMINANT 3B", "Deafness, Autosomal Dominant 3B", "deafness, autosomal dominant 3B", "deafness, autosomal dominant 3b", "deafness, autosomal dominant type 3B", "autosomal dominant nonsyndromic deafness 3B", "GJB6 autosomal dominant nonsyndromic deafness", "autosomal dominant nonsyndromic hearing loss 3B", "autosomal dominant nonsyndromic deafness type 3B", "autosomal dominant nonsyndromic deafness caused by mutation in GJB6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 3B", "shortest_name_length": 6}
{"curie": "UMLS:C0278721", "names": ["NHL, lymphoblastic", "Lymphoblastic Lymphoma", "Adult Lymphoblastic Lymphoma", "adult lymphoblastic lymphoma", "lymphoma, adult lymphoblastic", "lymphoblastic lymphoma, adult", "Adult Precursor Lymphoblastic Lymphoma", "adult precursor lymphoblastic lymphoma", "non-Hodgkin's lymphoma, adult lymphoblastic", "diffuse lymphoblastic lymphoma, with or without convoluted cells"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Lymphoblastic Lymphoma", "shortest_name_length": 18}
{"curie": "MONDO:0011484", "names": ["CPVT1", "CVPT1", "arrhythmogenic right ventricular dysplasia 2", "ventricular tachycardia, stress-induced polymorphic", "catecholaminergic polymorphic ventricular tachycardia 1", "ventricular tachycardia, catecholaminergic polymorphic, 1", "Catecholaminergic Polymorphic Ventricular Tachycardia Type 1", "catecholaminergic polymorphic ventricular tachycardia type 1", "ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "catecholaminergic polymorphic ventricular tachycardia 1", "shortest_name_length": 5}
{"curie": "MONDO:0007669", "names": ["RCAD", "MODY5", "ADTKD3", "HNF1B-MODY", "MODY type 5", "ADTKD-HNF1B", "RCAD syndrome", "atypical FJHN", "FJHN atypical", "RCAD Syndrome", "FJHN, atypical", "FJHN, ATYPICAL", "CAKUT with diabetes", "CAKUT WITH DIABETES", "HNF1B-related nephropathy", "HNF1B monogenic diabetes mellitus", "renal cysts and diabetes syndrome", "Renal Cysts and Diabetes Syndrome", "Renal cysts and diabetes syndrome", "RENAL CYSTS AND DIABETES SYNDROME", "maturity-onset diabetes of the young type 5", "familial hypoplastic glomerulocystic kidney", "Maturity-onset diabetes of the young type 5", "maturity-onset diabetes of the Young, type 5", "Maturity-onset diabetes of the young, type 5", "GLOMERULOCYSTIC KIDNEY, FAMILIAL HYPOPLASTIC", "Maturity Onset Diabetes of the Young, Type 5", "glomerulocystic kidney, familial hypoplastic", "familial hypoplastic, glomerulocystic kidney", "MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 5", "maturity onset diabetes of the Young, type 5", "Familial hypoplastic, glomerulocystic kidney", "Glomerulocystic kidney, familial hypoplastic", "maturity-onset diabetes of the young - type 5", "HNF1B-related renal cysts and diabetes syndrome", "renal dysfunction-early-onset diabetes syndrome", "hypoplastic type glomerulocystic kidney disease", "Renal dysfunction-early-onset diabetes syndrome", "glomerulocystic kidney disease, hypoplastic type", "Glomerulocystic kidney disease, hypoplastic type", "GLOMERULOCYSTIC KIDNEY DISEASE, HYPOPLASTIC TYPE", "MODY5 - maturity-onset diabetes of the young type 5", "HNF1B (HNF1 homeobox B) monogenic diabetes mellitus", "atypical familial juvenile hyperuricemic nephropathy", "hyperuricemic nephropathy, familial juvenile, atypical", "Hyperuricemic nephropathy, familial juvenile, atypical", "HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, ATYPICAL", "Familial hypoplastic, glomerulocystic kidney (disorder)", "Maturity-onset diabetes of the young, type 5 (disorder)", "TUBULOINTERSTITIAL KIDNEY DISEASE, AUTOSOMAL DOMINANT, 3", "familial hypoplastic, glomerulocystic kidney (diagnosis)", "renal cysts-maturity-onset diabetes of the young syndrome", "maturity-onset diabetes of the young - type 5 (diagnosis)", "Hepatocyte Nuclear Factor 1-Beta-Associated Monogenic Diabetes", "hepatocyte nuclear Factor 1-beta-associated monogenic diabetes", "HNF1B-related autosomal dominant tubulointerstitial kidney disease", "congenital anomalies of the kidney and urinary tract with diabetes", "CONGENITAL ANOMALIES OF THE KIDNEY AND URINARY TRACT WITH DIABETES", "HNF1B-Related Autosomal Dominant Tubulointerstitial Kidney Disease", "HNF1B-MODY - HNF1 homeobox B maturity-onset diabetes of the young type 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal cysts and diabetes syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C1963745", "names": ["HAIR-AN syndrome", "HAIR-AN Syndrome", "Hyperandrogenic, insulin-resistant acanthosis nigricans syndrome", "Hyperandrogenism, Insulin Resistance, Acanthosis Nigricans Syndrome", "Hyperandrogenism (HA), insulin resistance (IR), and acanthosis nigricans (AN)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HAIR-AN syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0011223", "names": ["ALS4", "ALS 4", "amyotrophic lateral sclerosis 4", "dHMN with upper motor neuron signs", "SETX amyotrophic lateral sclerosis", "amyotrophic lateral sclerosis ALS4", "amyotrophic lateral sclerosis type 4", "Amyotrophic lateral sclerosis type 4", "amyotrophic lateral sclerosis 4, juvenile", "AMYOTROPHIC LATERAL SCLEROSIS 4, JUVENILE", "Amyotrophic Lateral Sclerosis 4, Juvenile", "ALS4 - amyotrophic lateral sclerosis type 4", "Amyotrophic lateral sclerosis type 4 (disorder)", "Amyotrophic lateral sclerosis type 4 (diagnosis)", "amyotrophic lateral sclerosis caused by mutation in SETX", "distal hereditary motor neuropathy with pyramidal features", "NEURONOPATHY, DISTAL HEREDITARY MOTOR, WITH PYRAMIDAL FEATURES", "Neuronopathy, Distal Hereditary Motor, With Pyramidal Features", "neuronopathy, distal hereditary motor, with pyramidal features", "Distal hereditary motor neuropathy with upper motor neuron signs", "distal hereditary motor neuropathy with upper motor neuron signs", "dHMN (distal hereditary motor neuropathy) with upper motor neuron signs"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyotrophic lateral sclerosis type 4", "shortest_name_length": 4}
{"curie": "MONDO:0009921", "names": ["Young-Maders syndrome", "Pseudotrisomy 13 syndrome", "PSEUDOTRISOMY 13 SYNDROME", "Pseudotrisomy 13 Syndrome", "PSEUDOTRISOMY 13 syndrome", "pseudo-trisomy 13 syndrome", "Pseudo-trisomy 13 syndrome", "pseudo trisomy 13 syndrome", "Pseudo trisomy 13 syndrome", "holoprosencephaly polydactyly syndrome", "Holoprosencephaly polydactyly syndrome", "holoprosencephaly-polydactyly syndrome", "Holoprosencephaly-Polydactyly Syndrome", "HOLOPROSENCEPHALY-POLYDACTYLY SYNDROME", "holoprosencephaly-postaxial polydactyly syndrome", "Holoprosencephaly-postaxial polydactyly syndrome", "Holoprosencephaly and postaxial polydactyly syndrome", "Holoprosencephaly and postaxial polydactyly syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "holoprosencephaly-postaxial polydactyly syndrome", "shortest_name_length": 21}
{"curie": "MONDO:0008520", "names": ["LBNBG", "Liebenberg Syndrome", "Liebenberg syndrome", "LIEBENBERG syndrome", "LIEBENBERG SYNDROME", "Brachydactyly with Joint Dysplasia", "Brachydactyly with joint dysplasia", "brachydactyly with joint dysplasia", "brachydactyly with Joint dysplasia", "BRACHYDACTYLY WITH JOINT DYSPLASIA", "brachydactyly elbow wrist dysplasia", "Brachydactyly elbow wrist dysplasia", "brachydactyly-joint dysplasia syndrome", "Brachydactyly-joint dysplasia syndrome", "brachydactyly-elbow wrist dysplasia syndrome", "Brachydactyly-elbow wrist dysplasia syndrome", "Brachydactyly elbow wrist dysplasia (disorder)", "carpal synostosis with dysplastic elbow joints and brachydactyly", "synostosis, carpal, with dysplastic elbow joints and brachydactyly", "Synostosis, Carpal, with Dysplastic Elbow Joints and Brachydactyly", "SYNOSTOSIS, CARPAL, WITH DYSPLASTIC ELBOW JOINTS AND BRACHYDACTYLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly-elbow wrist dysplasia syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0014955", "names": ["RDEOA", "RCBTB1-related retinopathy", "RETINAL DYSTROPHY WITH OR WITHOUT EXTRAOCULAR ANOMALIES", "retinal dystrophy with or without extraocular anomalies", "Retinal Dystrophy with or without Extraocular Anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "RCBTB1-related retinopathy", "shortest_name_length": 5}
{"curie": "MONDO:0001330", "names": ["PRESBYOPIA", "Presbyopia", "presbyopia", "Presbyopias", "Presbyopia (disorder)", "presbyopia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "presbyopia", "shortest_name_length": 10}
{"curie": "MONDO:0021808", "names": ["ACD", "Acute cholinergic dysautonomia", "acute cholinergic dysautonomia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute cholinergic dysautonomia", "shortest_name_length": 3}
{"curie": "MONDO:0006015", "names": ["WFS", "ADRENAL HEMORRHAGE SYNDROME", "adrenal hemorrhage syndrome", "Meningococcic adrenal syndrome", "MENINGOCOCCIC ADRENAL SYNDROME", "Meningococcal adrenal syndrome", "Waterhouse-Friderichsen disease", "Waterhouse Friderichsen Syndrome", "waterhouse-friderichsen syndrome", "waterhouse friderichsen syndrome", "friderichsen-waterhouse syndrome", "WATERHOUSE-FRIDERICHSEN SYNDROME", "Waterhouse-Friderichsen Syndrome", "Waterhouse-Friderichsen syndrome", "Friderichsen-Waterhouse syndrome", "syndrome waterhouse friderichsen", "WATERHOUSE FRIDERICHSEN SYNDROME", "Waterhouse–Friderichsen syndrome", "Waterhouse Friederichsen Syndrome", "Waterhouse-Friederichsen Syndrome", "Waterhouse-Friderichsen syndrome NOS", "meningococcal hemorrhagic adrenalitis", "Waterhouse-Friderichsen syndrome, NOS", "Meningococcal Hemorrhagic Adrenalitis", "Meningococcal hemorrhagic adrenalitis", "Meningococcal haemorrhagic adrenalitis", "Hemorrhagic Adrenalitis, Meningococcal", "Adrenalitis, Meningococcal Hemorrhagic", "Meningococcal Hemorrhagic Adrenalitides", "Hemorrhagic Adrenalitides, Meningococcal", "Adrenalitides, Meningococcal Hemorrhagic", "Meningococcal Waterhouse-Friderichsen Syndrome", "Meningococcal Waterhouse Friderichsen Syndrome", "Meningococcal Waterhouse-Friderichsen syndrome", "Waterhouse-Friderichsen Syndrome, Meningococcal", "Syndrome, Meningococcal Waterhouse-Friderichsen", "Waterhouse-Friderichsen syndrome, meningococcal", "Acute adrenal insufficiency with meningococcemia", "Acute adrenal insufficiency with meningococcaemia", "fatal pneumococcal Waterhouse-Friderichsen syndrome", "Fulminant Meningococcal Sepsis with Adrenal Apoplexy", "Purpura Fulminans (Waterhouse-Friderichsen Syndrome)", "meningococcemia with Waterhouse-Friderichsen syndrome", "Acute adrenal insufficiency with meningococcal septicemia", "Acute adrenal insufficiency with meningococcal septicaemia", "Acute adrenal insufficiency with meningococcemia (disorder)", "meningococcemia with Waterhouse-Friderichsen syndrome (diagnosis)", "meningococcus; infection, adrenalitis, hemorrhagic (manifestation)", "infection; meningococcal, adrenalitis, hemorrhagic (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Waterhouse-Friderichsen syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0011496", "names": ["NHD", "OSCDP", "Namaqualand hip dysplasia", "NAMAQUALAND HIP DYSPLASIA", "Namaqualand hip dysplasia (disorder)", "osteoarthritis with mild chondrodysplasia", "Osteoarthritis with Mild Chondrodysplasia", "OSTEOARTHRITIS WITH MILD CHONDRODYSPLASIA", "mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early-onset osteoarthritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early-onset osteoarthritis", "shortest_name_length": 3}
{"curie": "MONDO:0019064", "names": ["FSP", "SPG", "HSP", "Strumpell disease", "spastic paraplegia", "Strumpell-Lorrain disease", "Strümpell-Lorrain disease", "French settlement disease", "Familial spastic paraplegia", "familial spastic paraplegia", "familial spastic paraparesis", "paralysis; familial, spastic", "hereditary spastic paraplegia", "Spastic congenital paraplegia", "Hereditary Spastic Paraplegia", "Hereditary spastic paraplegia", "spastic paraplegia hereditary", "hereditary spastic paraparesis", "PARAPLEGIA, SPASTIC HEREDITARY", "spastic; paralysis, hereditary", "Hereditary spastic paraparesis", "paralysis; spastic, hereditary", "Paraplegia, Hereditary Spastic", "Spastic Paraplegia, Hereditary", "Hereditary Spastic Paraplegias", "hereditary spastic paraplegias", "PARAPLEGIA, SPASTIC CONGENITAL", "congenital; paraplegia, spastic", "Paraplegias, Hereditary Spastic", "Paraplegia, Spastic, Hereditary", "spastic; paraplegia, hereditary", "Spastic Paraplegias, Hereditary", "paraplegia; spastic, hereditary", "PARAPLEGIA, SPASMODIC INFANTILE", "PARALYSIS, SPASTIC SPINAL FAMILIAL", "HSP - Hereditary spastic paraplegia", "Familial spastic paraplegia syndrome", "Hereditary spastic paraplegia (disorder)", "Spastic Paraplegia Hypertrophic Motor Sensory Neuropathy", "Hypertrophic Motor-Sensory Neuropathy-Spastic Paraplegia", "Spastic Paraplegia-Hypertrophic Motor-Sensory Neuropathy", "Hypertrophic Motor Sensory Neuropathy Spastic Paraplegia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia", "shortest_name_length": 3}
{"curie": "MONDO:0004201", "names": ["Pituitary hypoplasia", "Pituitary Hypoplasia", "hypoplasia pituitary", "pituitary hypoplasia", "hypoplasia; pituitary", "pituitary; hypoplasia", "pituitary gland hypoplasia", "Pituitary Gland Hypoplasia", "Pituitary gland hypoplasia", "Anterior pituitary hypoplasia", "Underdeveloped pituitary gland", "Hypoplasia of anterior pituitary", "Hypoplasia of the pituitary gland", "Hypoplasia of the anterior pituitary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pituitary hypoplasia", "shortest_name_length": 20}
{"curie": "MONDO:0020434", "names": ["osASD", "ostium secundum ASD", "ASD ostium secundum type", "ASD, ostium secundum type", "ostium secundum atrial septal defect", "atrial septal defect, ostium secundum type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial septal defect, ostium secundum type", "shortest_name_length": 5}
{"curie": "MONDO:0020461", "names": ["epiblepharon", "Epiblepharon", "congenital epiblepharon", "Congenital epiblepharon", "Epiblepharon (disorder)", "congenital epiblepharon (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epiblepharon", "shortest_name_length": 12}
{"curie": "UMLS:C0948349", "names": ["respiratory tract congestion", "Respiratory tract congestion", "Respiratory tract congestion (disorder)", "respiratory tract congestion (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Respiratory tract congestion", "shortest_name_length": 28}
{"curie": "UMLS:C0854821", "names": ["Refractory Anaplastic Large Cell Lymphoma", "Anaplastic large cell lymphoma T- and null-cell types refractory", "Anaplastic Large Cell Lymphoma T- and Null-cell Types Refractory"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anaplastic large cell lymphoma T- and null-cell types refractory", "shortest_name_length": 41}
{"curie": "UMLS:C4727192", "names": ["Refractory Bile Duct Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Bile Duct Carcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0011507", "names": ["diabetes mellitus, congenital autoimmune", "Diabetes Mellitus, Congenital Autoimmune", "DIABETES MELLITUS, CONGENITAL AUTOIMMUNE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diabetes mellitus, congenital autoimmune", "shortest_name_length": 40}
{"curie": "MONDO:0018769", "names": ["isosporosis", "Isosporosis", "isosporiasis", "ISOSPORIASIS", "Isosporiases", "Isosporiasis", "cystoisosporiasis", "Cystoisosporiasis", "Isospora Infection", "Isospora infections", "Isospora Infections", "Infection, Isospora", "Isosporiasis (disorder)", "isosporiasis (diagnosis)", "Cystoisospora belli infectious disease", "Cystoisospora belli disease or disorder", "Cystoisospora belli caused disease or disorder", "infection by Isospora belli and Isospora hominis", "Infection by Isospora belli and Isospora hominis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isosporiasis", "shortest_name_length": 11}
{"curie": "UMLS:C4721797", "names": ["stage II hypopharyngeal cancer", "Stage II Hypopharynx Carcinoma", "Stage II Carcinoma of Hypopharynx", "Stage II Hypopharyngeal Carcinoma", "Stage II Carcinoma of the Hypopharynx", "Stage II Hypopharyngeal Throat Cancer", "Stage II Hypopharyngeal Carcinoma AJCC v7", "Stage II Hypopharyngeal Carcinoma AJCC v6", "Stage II Hypopharyngeal Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Hypopharyngeal Carcinoma AJCC v6 and v7", "shortest_name_length": 30}
{"curie": "UMLS:C1721093", "names": ["Necrotic DNA Degradation", "DNA Degradation, Necrotic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DNA Degradation, Necrotic", "shortest_name_length": 24}
{"curie": "UMLS:C3272826", "names": ["Colorectal Burkitt Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Burkitt Lymphoma", "shortest_name_length": 27}
{"curie": "MONDO:0011534", "names": ["HMSNR", "Cmt4g", "CMT4G", "Charcot-Marie-Tooth disease type 4G", "CHARCOT-MARIE-TOOTH DISEASE, TYPE 4G", "Charcot-Marie-Tooth disease, type 4g", "Charcot-Marie-Tooth disease, type 4G", "HK1 Charcot-Marie-Tooth disease type 4", "Charcot-Marie-Tooth neuropathy type 4G", "Charcot-Marie-Tooth neuropathy, type 4G", "Charcot-Marie-Tooth Neuropathy, Type 4g", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4G", "Charcot-Marie-Tooth disease type 4G (disorder)", "Hereditary motor and sensory neuropathy Russe type", "hereditary motor and sensory neuropathy Russe type", "HEREDITARY MOTOR AND SENSORY NEUROPATHY, RUSSE TYPE", "Hereditary motor and sensory neuropathy, Russe type", "Hereditary motor and sensory neuropathy, Russe Type", "hereditary motor and sensory neuropathy, Russe type", "NEUROPATHY, HEREDITARY MOTOR AND SENSORY, RUSSE TYPE", "Neuropathy, hereditary motor and sensory, Russe type", "neuropathy, hereditary motor and sensory, Russe type", "autosomal recessive Charcot-Marie-Tooth disease type 4G", "Charcot-Marie-Tooth disease, autosomal recessive, type 4g", "CHARCOT-MARIE-TOOTH DISEASE, AUTOSOMAL RECESSIVE, TYPE 4G", "Charcot-Marie-Tooth disease, autosomal recessive, type 4G", "Charcot-Marie-Tooth disease type 4 caused by mutation in HK1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 4G", "shortest_name_length": 5}
{"curie": "UMLS:C0302356", "names": ["hemicrania", "Hemicrania", "hemianencephaly", "Hemianencephaly", "Partial Anencephaly", "Anencephaly, Partial", "Partial Anencephalies", "Anencephalies, Partial", "Incomplete Anencephaly", "Incomplete anencephaly", "anencephaly incomplete", "incomplete anencephaly", "Anencephaly, Incomplete", "Hemicranial Anencephaly", "Anencephaly, Hemicranial", "Hemianencephaly (disorder)", "hemianencephaly (diagnosis)", "Incomplete anencephaly (disorder)", "incomplete anencephaly (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Incomplete Anencephaly", "shortest_name_length": 10}
{"curie": "MONDO:0032746", "names": ["HYDM3", "HYDATIDIFORM MOLE, RECURRENT, 3", "hydatidiform mole, recurrent, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hydatidiform mole, recurrent, 3", "shortest_name_length": 5}
{"curie": "MONDO:0008572", "names": ["THYP", "Werner mesomelic syndrome", "Polydactyly with absent tibia", "polydactyly with absent tibia", "absent tibia-polydactyly syndrome", "absence of tibia with polydactyly", "Absence of tibia with polydactyly", "Tibia, Absence of, with Polydactyly", "Tibia, Hypoplasia of, with Polydactyly", "hypoplastic or aplastic tibia with polydactyly", "TIBIA, HYPOPLASIA OR APLASIA OF, WITH POLYDACTYLY", "hypoplastic tibiae-postaxial polydactyly syndrome", "tibia, hypoplasia or aplasia of, with polydactyly", "Hypoplastic tibia and postaxial polydactyly syndrome", "tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome", "Bilateral hypoplasia of tibia and postaxial polydactyly syndrome", "tibial hemimelia-polydactyly-triphalangeal thumbs with fibular dimelia", "Tibial Hemimelia-Polydactyly-Triphalangeal Thumbs with Fibular Dimelia", "TIBIAL HEMIMELIA-POLYDACTYLY-TRIPHALANGEAL THUMBS WITH FIBULAR DIMELIA", "Bilateral hypoplasia of tibia and postaxial polydactyly syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tibia, hypoplasia or aplasia of, with polydactyly", "shortest_name_length": 4}
{"curie": "UMLS:C4527183", "names": ["Stage IIC", "Stage IIC Cutaneous (Skin) Melanoma", "Pathologic Stage IIC Cutaneous Melanoma AJCC v8", "Pathologic Stage IIC Melanoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IIC Cutaneous Melanoma AJCC v8", "shortest_name_length": 9}
{"curie": "MONDO:0800099", "names": ["LCA13", "retinitis pigmentosa 53", "Leber congenital amaurosis 13", "RDH12 Leber congenital amaurosis", "Leber congenital amaurosis type 13", "RDH12-related recessive retinopathy", "Leber congenital amaurosis caused by mutation in RDH12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "RDH12-related recessive retinopathy", "shortest_name_length": 5}
{"curie": "MONDO:0001804", "names": ["Anterior scleritis", "anterior scleritis", "Anterior scleritis (disorder)", "anterior scleritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anterior scleritis", "shortest_name_length": 18}
{"curie": "MONDO:0011063", "names": ["Christianson-Fourie syndrome", "Christianson Fourie syndrome", "Hidrotic ectodermal dysplasia Christianson Fourie type", "hidrotic ectodermal dysplasia, Christianson-Fourie type", "Hidrotic ectodermal dysplasia, Christianson-Fourie type", "ectodermal dysplasia, hidrotic, Christianson-Fourie type", "ECTODERMAL DYSPLASIA, HIDROTIC, CHRISTIANSON-FOURIE TYPE", "Ectodermal dysplasia, hidrotic, Christianson-Fourie type", "Hidrotic ectodermal dysplasia Christianson Fourie type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hidrotic ectodermal dysplasia, Christianson-Fourie type", "shortest_name_length": 28}
{"curie": "UMLS:C0752110", "names": ["CNS Metabolic Disorders, Inborn", "Metabolic Disorders, CNS, Inborn", "Central Nervous System Inborn Metabolic Diseases", "Central Nervous System Inborn Metabolic Disorders", "Metabolic Diseases, Inborn, Central Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Inborn Metabolic Diseases", "shortest_name_length": 31}
{"curie": "MONDO:0008011", "names": ["MSK2", "Msk2", "ANTIGEN DEFINED BY MONOCLONAL ANTIBODY T87", "antigen defined by monoclonal antibody T87"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "antigen defined by monoclonal antibody T87", "shortest_name_length": 4}
{"curie": "UMLS:C1709669", "names": ["Primary Systemic Mastocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Systemic Mastocytosis", "shortest_name_length": 29}
{"curie": "MONDO:0018832", "names": ["HTRA1-related autosomal dominant cerebral angiopathy", "HTRA1-related autosomal dominant cerebral small vessel disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HTRA1-related autosomal dominant cerebral small vessel disease", "shortest_name_length": 52}
{"curie": "UMLS:C0853237", "names": ["Hypothalamo-pituitary disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypothalamo-pituitary disorder", "shortest_name_length": 30}
{"curie": "MONDO:0015333", "names": ["progeroid disease", "progeroid syndrome", "progeroid syndromes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progeroid syndrome", "shortest_name_length": 17}
{"curie": "UMLS:C4727013", "names": ["Resectable Soft Tissue Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Soft Tissue Sarcoma", "shortest_name_length": 30}
{"curie": "MONDO:0008955", "names": ["COFS1", "COFS syndrome", "ERCC6 COFS syndrome", "Pena-Shokeir syndrome, type 2", "Cerebrooculofacioskeletal Syndrome 1", "cerebrooculofacioskeletal syndrome 1", "cerebrooculofacioskeletal syndrome type 1", "COFS syndrome caused by mutation in ERCC6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebrooculofacioskeletal syndrome 1", "shortest_name_length": 5}
{"curie": "MONDO:0032660", "names": ["SMALED2B", "spinal muscular atrophy with lower extremity predominant 2B", "spinal muscular atrophy with lower extremity predominance 2B", "spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant", "SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2B, PRENATAL ONSET, AUTOSOMAL DOMINANT", "spinal muscular atrophy, lower extremity-predominant, 2b, prenatal onset, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal muscular atrophy, lower extremity-predominant, 2b, prenatal onset, autosomal dominant", "shortest_name_length": 8}
{"curie": "UMLS:C2981369", "names": ["Stage IB Esophageal Squamous Cell Cancer", "Stage IB Esophageal Squamous Cell Carcinoma", "Stage IB Esophageal Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Esophageal Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 40}
{"curie": "MONDO:0009006", "names": ["C2D", "C2 deficiency", "C2 DEFICIENCY", "C2 Deficiency", "C2 complement deficiency", "complement component 2 deficiency", "COMPLEMENT COMPONENT 2 DEFICIENCY", "complement deficiency caused by mutation in C2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complement component 2 deficiency", "shortest_name_length": 3}
{"curie": "UMLS:C1336013", "names": ["SLL with Unmutated IGVH", "Pregerminal Center Small Lymphocytic Lymphoma", "Small Lymphocytic Lymphoma with Unmutated Immunoglobulin Heavy Chain Variable-Region Gene"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Lymphocytic Lymphoma with Unmutated Immunoglobulin Heavy Chain Variable-Region Gene", "shortest_name_length": 23}
{"curie": "UMLS:C4743577", "names": ["Resectable Malignant Mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Malignant Mesothelioma", "shortest_name_length": 33}
{"curie": "UMLS:C1167727", "names": ["Postrenal failure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postrenal failure", "shortest_name_length": 17}
{"curie": "UMLS:C0273115", "names": ["lung injury", "injury lung", "Lung Injury", "Lung injury", "injury lungs", "lung; injury", "injury; lung", "Injury, Lung", "injuries lung", "Lung Injuries", "Injury of lung", "Injuries, Lung", "Lung injury NOS", "Pulmonary Injury", "Injury, Pulmonary", "Pulmonary Injuries", "Injuries, Pulmonary", "Traumatic lung injury", "lung injury (diagnosis)", "Injury of lung (disorder)", "Unspecified injury of lung", "Unspecified injury of lung, NOS", "Unspecified injury of lung, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Injury", "shortest_name_length": 11}
{"curie": "UMLS:C1707591", "names": ["Cutaneous T-Lymphoblastic Leukemia/Lymphoma", "Cutaneous T Lymphoblastic Leukemia/Lymphoma", "Cutaneous Precursor T-Lymphoblastic Lymphoma/Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous T Lymphoblastic Leukemia/Lymphoma", "shortest_name_length": 43}
{"curie": "UMLS:C2936665", "names": ["Late-Onset Immunoglobulin Deficiency", "Immunoglobulin Deficiency, Late-Onset", "Deficiency, Late-Onset Immunoglobulin", "Immunoglobulin Deficiency, Late Onset", "Late-Onset Immunoglobulin Deficiencies", "Immunoglobulin Deficiencies, Late-Onset", "Deficiencies, Late-Onset Immunoglobulin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immunoglobulin Deficiency, Late-Onset", "shortest_name_length": 36}
{"curie": "MONDO:0008842", "names": ["AOA", "AOA1", "EAOH", "EOCA-HA", "Ataxia-oculomotor apraxia 1", "ATAXIA-OCULOMOTOR APRAXIA 1", "ataxia-oculomotor apraxia 1", "ataxia-oculomotor apraxia type 1", "Ataxia-Oculomotor Apraxia Type 1", "Ataxia-oculomotor apraxia type 1", "Ataxia oculomotor apraxia type 1", "ATAXIA-OCULOMOTOR APRAXIA SYNDROME", "ataxia-oculomotor apraxia syndrome", "Ataxia-oculomotor apraxia syndrome", "ataxia-telangiectasia-like syndrome", "Ataxia-telangiectasia-like syndrome", "ATAXIA-TELANGIECTASIA-LIKE SYNDROME", "ataxia with oculomotor apraxia type 1", "AOA1 (ataxia oculomotor apraxia type 1)", "Ataxia, Adult-Onset, With Oculomotor Apraxia", "ataxia, adult-onset, with oculomotor apraxia", "ATAXIA, ADULT-ONSET, WITH OCULOMOTOR APRAXIA", "early-onset cerebellar ataxia with hypoalbuminemia", "Early-onset cerebellar ataxia with hypoalbuminemia", "cerebellar ataxia, early-onset, with hypoalbuminemia", "CEREBELLAR ATAXIA, EARLY-ONSET, WITH HYPOALBUMINEMIA", "Cerebellar Ataxia, Early-Onset, With Hypoalbuminemia", "APTX oculomotor apraxia or related oculomotor disease", "Autosomal recessive ataxia with oculomotor apraxia type 1", "early-onset ataxia with oculomotor apraxia and hypoalbuminemia", "Early-onset ataxia with oculomotor apraxia and hypoalbuminemia", "ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia", "ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA", "Ataxia, Early-Onset, With Oculomotor Apraxia And Hypoalbuminemia", "Early-Onset Ataxia with Ocular Motor Apraxia and Hypoalbuminemia", "Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia", "Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1", "oculomotor apraxia or related oculomotor disease caused by mutation in APTX", "Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia", "shortest_name_length": 3}
{"curie": "MONDO:0042973", "names": ["familial osteosclerosis", "hereditary osteosclerosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial osteosclerosis", "shortest_name_length": 23}
{"curie": "MONDO:0005385", "names": ["Aneurysm", "ANEURYSM", "aneurysm", "aneurysms", "ANEURYSMS", "Aneurysms", "Angiopathy", "angiopathy", "vasculopathy", "Vasculopathy", "Aneurysm, NOS", "Angiopathy, NOS", "vascular disease", "VASCULAR DISEASE", "vascular problem", "Vascular Disease", "Vascular disease", "VASCULAR PROBLEM", "vascular disorder", "Disorder vascular", "VASCULAR DISEASES", "vascular diseases", "Vascular disorder", "Vascular Diseases", "Disease, Vascular", "DISORDER VASCULAR", "Vascular Disorder", "Aneurysm - lesion", "VASCULAR DISORDER", "Vascular Disorders", "vascular disorders", "vascular; disorder", "artery; dilatation", "Vascular disorders", "disorder; vascular", "Aneurysmal disease", "Diseases, Vascular", "Vascular dilatation", "Aneurysm (disorder)", "vasculature disease", "blood vessel disease", "VASCULAR_NOS PROBLEM", "aneurysmal dilatation", "Aneurysmal dilatation", "Vascular disorder NOS", "blood vessel disorder", "VASCULAR PROBLEM, NOS", "Vascular disease, NOS", "disease of vasculature", "Vascular disorder, NOS", "disorder of vasculature", "Blood-vessels--Diseases", "blood vessels; disorder", "vascular tissue disease", "Disorder of blood vessel", "vascular system disorders", "Aneurysmal dilatation, NOS", "Aneurysm of unspecified site", "Unspecified Vascular Problem", "Vascular disease or syndrome", "aneurysm of unspecified site", "Spinal Cord Vascular Diseases", "Vascular Diseases, Spinal Cord", "Vascular Diseases and Syndromes", "vasculature disease or disorder", "disease (or disorder); vascular", "Wider than typical opening or gap", "VASCULAR (EXTRACARDIAC) DISORDERS", "Aneurysm (morphologic abnormality)", "disease or disorder of vasculature", "Disorder of blood vessel (disorder)", "disease (or disorder); blood vessels", "vascular system disorders (diagnosis)", "aneurysm of unspecified site (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vascular disorder", "shortest_name_length": 8}
{"curie": "MONDO:0011473", "names": ["LCA5", "Leber Congenital Amaurosis 5", "Leber congenital amaurosis 5", "LEBER CONGENITAL AMAUROSIS 5", "LCA5 Leber congenital amaurosis", "Leber congenital amaurosis type 5", "Leber congenital amaurosis, type 5", "amaurosis congenita of Leber, type 5", "Amaurosis congenita of Leber, type 5", "Leber congenital amaurosis caused by mutation in LCA5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leber congenital amaurosis 5", "shortest_name_length": 4}
{"curie": "MONDO:0011106", "names": ["FDLAB", "FDLAB syndrome", "TRABOULSI SYNDROME", "Traboulsi syndrome", "SHAWAF-TRABOULSI SYNDROME", "ECTOPIA LENTIS, SPONTANEOUS FILTERING BLEBS, AND CRANIOFACIAL DYSMORPHISM", "ectopia lentis, spontaneous filtering blebs, and craniofacial Dysmorphism", "Ectopia Lentis, Spontaneous Filtering Blebs, and Craniofacial Dysmorphism", "facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs", "FACIAL DYSMORPHISM, LENS DISLOCATION, ANTERIOR SEGMENT ABNORMALITIES, AND SPONTANEOUS FILTERING BLEBS", "facial dysmorphism-lens dislocation-anterior segment abnormalities-spontaneous filtering blebs syndrome", "Facial dysmorphism-lens dislocation-anterior segment abnormalities-spontaneous filtering blebs syndrome", "Facial dysmorphism, lens dislocation, anterior segment abnormalities, spontaneous filtering bleb syndrome", "Facial dysmorphism-lens dislocation-anterior segment abnormalities-nontraumatic conjunctive cysts syndrome", "facial dysmorphism-lens dislocation-anterior segment abnormalities-nontraumatic conjunctive cysts syndrome", "Facial dysmorphism, lens dislocation, anterior segment abnormalities, nontraumatic conjunctive cyst syndrome", "FDLAB (facial dysmorphism, lens dislocation, anterior segment abnormalities, spontaneous filtering bleb) syndrome", "Facial dysmorphism, lens dislocation, anterior segment abnormalities, spontaneous filtering bleb syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "facial dysmorphism-lens dislocation-anterior segment abnormalities-spontaneous filtering blebs syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0520676", "names": ["pmdd", "PMDD", "premenstrual disorder", "Premenstrual dysphoric disorder", "Premenstrual Dysphoric Syndrome", "Premenstrual Dysphoric Disorder", "premenstrual dysphoric disorder", "disorder dysphoric premenstrual", "Dysphoric Disorder, Premenstrual", "Disorder, Premenstrual Dysphoric", "Syndrome, Premenstrual Dysphoric", "Premenstrual dysphoric disorder (disorder)", "premenstrual dysphoric disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Premenstrual Dysphoric Disorder", "shortest_name_length": 4}
{"curie": "MONDO:0015666", "names": ["Familial idiopathic dilation of right atrium", "Familial idiopathic dilatation of right atrium", "Familial idiopathic dilatation of the right atrium", "familial idiopathic dilatation of the right atrium", "Familial idiopathic dilatation of right atrium (disorder)", "familial idiopathic dilatation of the right atrium (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial idiopathic dilatation of the right atrium", "shortest_name_length": 44}
{"curie": "UMLS:C0410158", "names": ["Muscle damage", "muscle damage", "damage muscle", "damage muscles", "damages muscles"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Muscle damage", "shortest_name_length": 13}
{"curie": "UMLS:C1332048", "names": ["AIDS-Related Kaposi Sarcoma-Associated Human Herpes Virus 8 Positive Extracavity Lymphoma", "AIDS-Related Kaposi's Sarcoma-Associated Human Herpes Virus 8 Positive Extracavity Lymphoma", "AIDS-Related Large B-Cell Lymphoma Arising in HHV8-Associated Multicentric Castleman Disease", "AIDS-Related Large B-Cell Lymphoma Arising in HHV 8-Associated Multicentric Castleman Disease", "AIDS-Related Diffuse Large B-Cell Lymphoma Arising in HHV8-Positive Multicentric Castleman Disease", "AIDS-Related Large B-Cell Lymphoma Arising in Human Herpes Virus 8-Associated Multicentric Castleman Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Diffuse Large B-Cell Lymphoma Arising in HHV8-Positive Multicentric Castleman Disease", "shortest_name_length": 89}
{"curie": "MONDO:0002541", "names": ["spinal cord oligodendroglioma", "Spinal Cord Oligodendroglioma", "Oligodendroglioma of Spinal Cord", "oligodendroglioma of spinal cord", "Oligodendroglioma of spinal cord", "Oligodendroglioma of spinal cord (disorder)", "oligodendroglioma of spinal cord (diagnosis)", "Well Differentiated Spinal Cord Oligodendroglioma", "Well differentiated Spinal Cord Oligodendroglioma", "well differentiated spinal cord oligodendroglioma", "well differentiated spinal cord oligodendroglial tumor", "Well Differentiated Spinal Cord Oligodendroglial Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal cord oligodendroglioma", "shortest_name_length": 29}
{"curie": "UMLS:C1336061", "names": ["Splenic Manifestation of B-Cell Prolymphocytic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Splenic Manifestation of B-Cell Prolymphocytic Leukemia", "shortest_name_length": 55}
{"curie": "UMLS:C0395955", "names": ["noise-induced tinnitus", "Noise-induced tinnitus", "Noise Induced Tinnitus", "Induced Tinnitus, Noise", "Tinnitus, Noise Induced", "Noise-induced tinnitus (disorder)", "noise-induced tinnitus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tinnitus, Noise Induced", "shortest_name_length": 22}
{"curie": "MONDO:0014338", "names": ["CVID11", "IL21 deficiency", "IL21 DEFICIENCY", "IL21 Deficiency", "IL21-related infantile IBD", "common variable immunodeficiency 11", "Immunodeficiency, Common Variable, 11", "IMMUNODEFICIENCY, COMMON VARIABLE, 11", "immunodeficiency, common variable, 11", "immunodeficiency, common variable, type 11", "IL21-related infantile inflammatory bowel disease", "Interleukin 21 related infantile inflammatory bowel disease", "Interleukin 21 related infantile inflammatory bowel disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IL21-related infantile inflammatory bowel disease", "shortest_name_length": 6}
{"curie": "MONDO:0011816", "names": ["LATHOS", "Lathosterolosis", "Sc5D deficiency", "LATHOSTEROLOSIS", "SC5D DEFICIENCY", "lathosterolosis", "Lathosterolosis (disorder)", "Sterol C5-Desaturase Deficiency", "Sterol C5-desaturase deficiency", "STEROL C5-DESATURASE DEFICIENCY", "sterol C5-desaturase deficiency", "Sterol C5 desaturase deficiency", "3-beta-hydroxysteroid-delta(5)-desaturase deficiency", "Deficiency of 3-beta-hydroxysteroid-delta(5)-desaturase"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lathosterolosis", "shortest_name_length": 6}
{"curie": "MONDO:0011936", "names": ["MCOPS6", "Bakrania Ragge syndrome", "Bakrania-Ragge syndrome", "microphthalmia syndromic 6", "syndromic microphthalmia 6", "microphthalmia, syndromic 6", "Microphthalmia, Syndromic 6", "MICROPHTHALMIA, SYNDROMIC 6", "Syndromic microphthalmia type 6", "syndromic microphthalmia type 6", "microphthalmia, syndromic type 6", "MICROPHTHALMIA AND PITUITARY ANOMALIES", "microphthalmia and pituitary anomalies", "Microphthalmia And Pituitary Anomalies", "Microphthalmia with brain and digit anomaly", "Microphthalmia with brain and digit anomalies", "microphthalmia with brain and digit anomalies", "Microphthalmia with brain and digit anomaly (disorder)", "Microphthalmia With Brain And Digit Developmental Anomalies", "microphthalmia with brain and digit developmental anomalies", "MICROPHTHALMIA WITH BRAIN AND DIGIT DEVELOPMENTAL ANOMALIES", "anophthalmia clinical with micrognathia malformed ears digital anomalies and abnormal external genitalia", "ANOPHTHALMIA, CLINICAL, WITH MICROGNATHIA, MALFORMED EARS, DIGITAL ANOMALIES, AND ABNORMAL EXTERNAL GENITALIA", "Anophthalmia, Clinical, With Micrognathia, Malformed Ears, Digital Anomalies, And Abnormal External Genitalia", "anophthalmia, clinical, with micrognathia, malformed ears, digital anomalies, and abnormal external genitalia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microphthalmia with brain and digit anomalies", "shortest_name_length": 6}
{"curie": "MONDO:0012058", "names": ["Mci2", "MCI2", "myocardial infarction, susceptibility to, 2", "MYOCARDIAL INFARCTION, SUSCEPTIBILITY TO, 2", "myocardial infarction, susceptibility to, type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myocardial infarction, susceptibility to, 2", "shortest_name_length": 4}
{"curie": "MONDO:0013526", "names": ["EPM6", "PME type 6", "progressive myoclonus epilepsy 6", "epilepsy, progressive myoclonic 6", "epilepsy, progressive myoclonic, 6", "EPILEPSY, PROGRESSIVE MYOCLONIC, 6", "GOSR2 progressive myoclonic epilepsy", "progressive myoclonus epilepsy type 6", "Progressive myoclonic epilepsy type 6", "progressive myoclonic epilepsy type 6", "Progressive myoclonus epilepsy type 6", "epilepsy, progressive myoclonic, type 6", "North Sea progressive myoclonus epilepsy", "GOSR2-related progressive myoclonus ataxia", "progressive familial myoclonic epilepsy type 6", "Progressive myoclonic epilepsy type 6 (disorder)", "PME type 6 - progressive myoclonic epilepsy type 6", "progressive familial myoclonic epilepsy type 6 (diagnosis)", "progressive myoclonic epilepsy caused by mutation in GOSR2", "GOSR2 (golgi SNAP receptor complex member 2) related progressive myoclonus ataxia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive myoclonic epilepsy type 6", "shortest_name_length": 4}
{"curie": "MONDO:0017604", "names": ["MZL", "MZBCL", "Marginal zone lymphoma", "Marginal Zone Lymphoma", "marginal zone lymphoma", "Marginal zone lymphoma, NOS", "Marginal Zone B-Cell Lymphoma", "Marginal zone B-cell lymphoma", "marginal zone B cell lymphoma", "marginal zone B-cell lymphoma", "lymphoma of marginal zone B cell", "Marginal zone lymphoma (disorder)", "marginal zone lymphoma (diagnosis)", "marginal zone B-cell lymphoma (diagnosis)", "Marginal zone B-cell lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "marginal zone lymphoma", "shortest_name_length": 3}
{"curie": "UMLS:C5239075", "names": ["Advanced Round Cell Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Round Cell Liposarcoma", "shortest_name_length": 31}
{"curie": "MONDO:0013744", "names": ["CCA5", "CTRCT37", "cataract 37", "CATARACT 37", "cataract type 37", "cataract 37, autosomal dominant", "congenital cataract cerulean type 5", "CATARACT, CONGENITAL, CERULEAN TYPE, 5", "cataract, congenital, cerulean type, 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 37", "shortest_name_length": 4}
{"curie": "MONDO:0012412", "names": ["C7D", "C7 deficiency", "C7 DEFICIENCY", "C7 Deficiency", "COMPLEMENT COMPONENT 7 DEFICIENCY", "Complement Component 7 Deficiency", "complement component 7 deficiency", "C7 classic complement early component deficiency", "classic complement early component deficiency caused by mutation in C7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complement component 7 deficiency", "shortest_name_length": 3}
{"curie": "UMLS:C0279743", "names": ["High Grade Salivary Gland Cancer", "high-grade salivary gland cancer", "salivary gland cancer, high grade", "High Grade Salivary Gland Carcinoma", "high-grade salivary gland carcinoma", "salivary gland carcinoma, high grade", "High-Grade Carcinoma of Salivary Gland", "cancer of the salivary gland, high grade", "High-Grade Carcinoma of the Salivary Gland", "carcinoma of the salivary gland, high grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Salivary Gland Carcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C1335917", "names": ["Sarcoma NCI Grade 2", "Sarcoma NCI Grade II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sarcoma NCI Grade 2", "shortest_name_length": 19}
{"curie": "MONDO:0016194", "names": ["qualitative or quantitative defects of nebulin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of nebulin", "shortest_name_length": 46}
{"curie": "MONDO:0007832", "names": ["INTERFERON ANTIVIRAL DEPRESSOR", "interferon antiviral depressor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "interferon antiviral depressor", "shortest_name_length": 30}
{"curie": "MONDO:0003108", "names": ["Cervicomedullary Junction Tumor", "cervicomedullary junction tumor", "Tumor of Cervicomedullary Junction", "Cervicomedullary Junction Neoplasm", "tumor of cervicomedullary junction", "cervicomedullary junction neoplasm", "Cervicomedullary Junction Neoplasms", "cervicomedullary junction neoplasms", "Neoplasm of Cervicomedullary Junction", "neoplasm of cervicomedullary junction", "tumor of the Cervicomedullary Junction", "Tumor of the Cervicomedullary Junction", "tumor of the cervicomedullary junction", "neoplasm of the cervicomedullary junction", "Neoplasm of the Cervicomedullary Junction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervicomedullary junction neoplasm", "shortest_name_length": 31}
{"curie": "UMLS:C5667179", "names": ["HIV-Related Lymphoproliferative Disorder", "HIV-Associated Lymphoproliferative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HIV-Related Lymphoproliferative Disorder", "shortest_name_length": 40}
{"curie": "MONDO:0010268", "names": ["XLAG", "XLISG", "XLIS2", "Xlisg", "LISX2", "XLAG syndrome", "X-linked lissencephaly 2", "lissencephaly, X-linked 2", "LISSENCEPHALY, X-LINKED, 2", "lissencephaly, X-linked, 2", "Lissencephaly, X-Linked, 2", "lissencephaly, X-linked, type 2", "HYDRANENCEPHALY AND ABNORMAL GENITALIA", "hydranencephaly and abnormal genitalia", "Hydranencephaly and Abnormal Genitalia", "hydranencephaly with abnormal genitalia", "HYDRANENCEPHALY WITH ABNORMAL GENITALIA", "X-linked lissencephaly with abnormal genitalia", "X-linked lissencephaly with ambiguous genitalia", "Lissencephaly, X-Linked, with Ambiguous Genitalia", "LISSENCEPHALY, X-LINKED, WITH AMBIGUOUS GENITALIA", "lissencephaly, X-linked, with ambiguous genitalia", "X-linked lissencephaly with abnormal genitalia syndrome", "XLAG (X-linked lissencephaly with abnormal genitalia) syndrome", "X-linked lissencephaly-corpus callosum agenesis-genital anomalies syndrome", "X-linked lissencephaly - agenesis of the corpus callosum - genital anomalies", "X-linked lissencephaly-agenesis of the corpus callosum-genital anomalies syndrome", "X-linked lissencephaly with agenesis of corpus callosum and genital anomaly syndrome", "X-linked lissencephaly with agenesis of corpus callosum and genital anomaly syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked lissencephaly with abnormal genitalia", "shortest_name_length": 4}
{"curie": "UMLS:C1883018", "names": ["SAA", "Severe Aplastic Anemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Severe Aplastic Anemia", "shortest_name_length": 3}
{"curie": "UMLS:C3160888", "names": ["Metastatic gastric adenocarcinoma", "Metastatic Gastric Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic gastric adenocarcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C4552674", "names": ["Stage I Penile Cancer", "Stage I Penile Cancer AJCC v8", "Stage I Penile Squamous Cell Carcinoma AJCC v8", "Stage I Squamous Cell Carcinoma of the Penis AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Penile Cancer AJCC v8", "shortest_name_length": 21}
{"curie": "UMLS:C0263332", "names": ["heat urticaria", "Urticaria heat", "Heat urticaria", "URTICARIA HEAT", "heat; urticaria", "urticaria; heat", "Thermal urticaria", "thermal urticaria", "Urticaria thermal", "urticaria; thermal", "thermal; urticaria", "Urticaria due to heat", "Urticaria thermal NOS", "Urticaria caused by heat", "heat urticaria (diagnosis)", "Urticaria caused by heat (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urticaria due to heat", "shortest_name_length": 14}
{"curie": "UMLS:C1257840", "names": ["Rectosigmoid Aganglionosis", "Aganglionosis, Rectosigmoid", "Rectosigmoid Colon Aganglionosis", "Aganglionosis, Rectosigmoid Colon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aganglionosis, Rectosigmoid Colon", "shortest_name_length": 26}
{"curie": "UMLS:C5446470", "names": ["Advanced Rectal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Rectal Adenocarcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0032715", "names": ["MRT69", "Mental Retardation, Autosomal Recessive 69", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 69", "autosomal recessive intellectual developmental disorder 69", "intellectual developmental disorder, autosomal recessive 69", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 69"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder, autosomal recessive 69", "shortest_name_length": 5}
{"curie": "MONDO:0030796", "names": ["leukoencephalopathy, hereditary diffuse, with spheroids"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukoencephalopathy, hereditary diffuse, with spheroids", "shortest_name_length": 55}
{"curie": "MONDO:0002894", "names": ["spinal chordoma", "Spinal Chordoma", "Spinal Chordomas", "spinal Chordomas", "Chordoma of Spine", "chordoma of spine", "Vertebral chordoma", "spinal column chordoma", "Spinal Column Chordoma", "chordoma of spinal column", "Chordoma of Spinal Column", "chordoma of the spinal column", "Chordoma of the Spinal Column"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal chordoma", "shortest_name_length": 15}
{"curie": "UMLS:C4745011", "names": ["Malignant Abdominal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Abdominal Neoplasm", "shortest_name_length": 28}
{"curie": "UMLS:C1336247", "names": ["Follicular lymphoma stage III", "Stage III Follicular Lymphoma", "Ann Arbor Stage III Follicular Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Follicular lymphoma stage III", "shortest_name_length": 29}
{"curie": "UMLS:C0751406", "names": ["Posttraumatic osteoporosis", "Post-Traumatic Osteoporoses", "Post-Traumatic Osteoporosis", "Post-traumatic osteoporosis", "Osteoporosis, Post Traumatic", "post-traumatic; osteoporosis", "Osteoporosis, post-traumatic", "osteoporosis; post-traumatic", "Osteoporosis, Post-Traumatic", "Posttraumatic atrophy of bone", "Posttraumatic osteoporosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post-Traumatic Osteoporosis", "shortest_name_length": 26}
{"curie": "MONDO:0000687", "names": ["pelade", "alopecia celsi", "ALOPECIA AREATA", "Alopecia areata", "ALOPECIA, CELSI", "alopecia areata", "Patchy alopecia", "areata alopecia", "patchy alopecia", "Alopecia Areata", "Patchy baldness", "diffuse alopecia", "patchy hair loss", "Patchy hair loss", "areata; alopecia", "alopecia diffuse", "ALOPECIA, AREATA", "Celsus' vitiligo", "alopecia; areata", "Vitiligo capitis", "Diffuse alopecia", "marginal alopecia", "Jonston's alopecia", "Cazenave's vitiligo", "Patchy loss of hair", "Multifocal alopecia", "AA - Alopecia areata", "Circumscribed alopecia", "Alopecia Circumscripta", "Alopecia circumscripta", "ALOPECIA CIRCUMSCRIPTA", "diffuse alopecia areata", "circumscripta; alopecia", "Diffuse alopecia areata", "alopecia; circumscripta", "Alopecia areata, diffuse", "Alopecia areata (disorder)", "alopecia areata (diagnosis)", "Diffuse alopecia (disorder)", "patchy alopecia was observed", "Alopecia areata, unspecified", "diffuse alopecia was observed", "Diffuse alopecia areata (disorder)", "patchy alopecia (physical finding)", "diffuse alopecia (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diffuse alopecia areata", "shortest_name_length": 6}
{"curie": "UMLS:C5420535", "names": ["Non-Neoplastic Middle Ear Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Middle Ear Disorder", "shortest_name_length": 34}
{"curie": "MONDO:0007856", "names": ["TOC", "Toc", "Howel Evans syndrome", "howel-Evans syndrome", "Howell-Evans syndrome", "Howell Evans syndrome", "Howel-Evans' syndrome", "Howel-Evans-Clark syndrome", "Bennion-Patterson syndrome", "esophageal cancer with tylosis", "tylosis with esophageal cancer", "Tylosis with esophageal cancer", "TYLOSIS WITH ESOPHAGEAL CANCER", "tylosis - oesophageal carcinoma", "Howel-Evans' syndrome (disorder)", "Howel-Evans' syndrome (diagnosis)", "tylosis-oesophageal carcinoma syndrome", "Tylosis-oesophageal carcinoma syndrome", "Keratoderma with carcinoma of esophagus", "Keratoderma with carcinoma of oesophagus", "Keratosis palmoplantaris with esophageal cancer", "keratosis palmoplantaris with esophageal cancer", "palmoplantar keratoderma with esophageal cancer", "PALMOPLANTAR KERATODERMA WITH ESOPHAGEAL CANCER", "KERATOSIS PALMARIS ET PLANTARIS WITH ESOPHAGEAL CANCER", "keratosis palmaris et plantaris with esophageal cancer", "palmoplantar keratoderma-esophageal carcinoma syndrome", "Keratosis palmoplantaris-esophageal carcinoma syndrome", "Keratosis Palmaris Et Plantaris With Esophageal Cancer", "keratosis palmoplantaris-esophageal carcinoma syndrome", "keratosis palmaris Et plantaris with esophageal cancer", "Palmoplantar keratoderma-esophageal carcinoma syndrome", "Diffuse palmoplantar keratoderma with esophageal cancer", "Diffuse palmoplantar keratoderma with oesophageal cancer", "Palmoplantar hyperkeratosis-esophageal carcinoma syndrome", "palmoplantar hyperkeratosis-esophageal carcinoma syndrome", "hereditary palmoplantar keratoderma Howel-Evans' syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "palmoplantar keratoderma-esophageal carcinoma syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0012718", "names": ["COXPD5", "Combined Oxidative Phosphorylation Deficiency 5", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 5", "combined oxidative phosphorylation deficiency 5", "Combined oxidative phosphorylation defect type 5", "combined oxidative phosphorylation defect type 5", "Hypotonia with lactic acidemia and hyperammonemia", "hypotonia with lactic acidemia and hyperammonemia", "Hypotonia with lactic acidaemia and hyperammonaemia", "COXPD5 - combined oxidative phosphorylation defect 5", "MRPS22 combined oxidative phosphorylation deficiency", "combined oxidative phosphorylation deficiency type 5", "Combined oxidative phosphorylation defect type 5 (disorder)", "combined oxidative phosphorylation defect type 5 (diagnosis)", "combined oxidative phosphorylation deficiency caused by mutation in MRPS22"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotonia with lactic acidemia and hyperammonemia", "shortest_name_length": 6}
{"curie": "MONDO:0014673", "names": ["CTRCT44", "CATARACT 44", "cataract 44", "cataract type 44", "total early-onset cataract", "CATARACT 44 AND HYPOTRICHOSIS", "LSS early-onset non-syndromic cataract", "early-onset non-syndromic cataract caused by mutation in LSS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 44", "shortest_name_length": 7}
{"curie": "MONDO:0000994", "names": ["Phyllodes Tumor of the Prostate", "prostate malignant phyllodes tumor", "Malignant Prostate Phyllodes Tumor", "malignant prostate phyllodes tumor", "malignant prostate phyllodes neoplasm", "malignant phyllodes tumor of prostate", "Malignant Phyllodes Tumor of Prostate", "Malignant Prostate Phyllodes Neoplasm", "Malignant Phyllodes Neoplasm of Prostate", "malignant phyllodes neoplasm of prostate", "malignant phyllodes tumor of the prostate", "Malignant Phyllodes Tumor of the Prostate", "Malignant Phyllodes Neoplasm of the Prostate", "malignant phyllodes neoplasm of the prostate", "malignant Phyllodes neoplasm of the prostate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant prostate phyllodes tumor", "shortest_name_length": 31}
{"curie": "UMLS:C0751509", "names": ["Short Sleep Phenotype", "Phenotype, Short Sleep", "Short Sleep Phenotypes", "Short Sleeper Syndrome", "Short Sleeper Syndromes", "Sleeper Syndrome, Short", "Phenotypes, Short Sleep", "Syndrome, Short Sleeper", "Sleep Phenotypes, Short", "Syndromes, Short Sleeper", "Sleeper Syndromes, Short"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Short Sleeper Syndrome", "shortest_name_length": 21}
{"curie": "UMLS:C1299599", "names": ["psychosis; senile dementia", "psychosis; dementia, senile", "senile; dementia, psychosis", "Senile dementia with psychosis", "Senile dementia with psychosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Senile dementia with psychosis", "shortest_name_length": 26}
{"curie": "UMLS:C4727844", "names": ["Myeloid Neoplasms with Germline Predisposition Associated with Inherited Bone Marrow Failure Syndromes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myeloid Neoplasms with Germline Predisposition Associated with Inherited Bone Marrow Failure Syndromes", "shortest_name_length": 102}
{"curie": "UMLS:C5447647", "names": ["Advanced Lung Carcinoid Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Lung Carcinoid Tumor", "shortest_name_length": 29}
{"curie": "MONDO:0004708", "names": ["esophagus cancer, stage 0", "Stage 0 Esophageal Cancer", "stage 0 esophageal cancer", "esophageal cancer, stage 0", "severe esophageal dysplasia", "Severe Esophageal Dysplasia", "Cancer in situ of esophagus", "Severe esophageal dysplasia", "stage 0 esophagus carcinoma", "esophagus carcinoma in situ", "esophagus in situ carcinoma", "Esophageal carcinoma in situ", "Esophageal Carcinoma in situ", "oesophagus carcinoma in situ", "Esophageal carcinoma stage 0", "esophageal carcinoma in situ", "Cancer in situ of oesophagus", "Severe oesophageal dysplasia", "Oesophageal carcinoma in situ", "Oesophageal carcinoma stage 0", "carcinoma in situ of esophagus", "Carcinoma in situ of esophagus", "Carcinoma in situ of oesophagus", "carcinoma in situ of oesophagus", "Esophageal carcinoma NOS stage 0", "Stage 0 Esophageal Cancer AJCC v7", "stage 0 esophageal cancer aJCC v7", "Oesophageal carcinoma NOS stage 0", "stage 0 carcinoma of the esophagus", "Severe Esophageal Dysplasia AJCC v7", "Carcinoma in situ of esophagus, NOS", "severe esophageal dysplasia aJCC v7", "stage 0 carcinoma of the oesophagus", "esophageal carcinoma in situ aJCC v7", "stage 0 esophageal carcinoma in situ", "Esophageal Carcinoma in situ AJCC v7", "Carcinoma in situ of oesophagus, NOS", "Severe esophageal dysplasia (disorder)", "Carcinoma in situ of esophagus (disorder)", "carcinoma in situ of esophagus (diagnosis)", "Esophageal carcinoma site unspecified stage 0", "Oesophageal carcinoma site unspecified stage 0"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophagus carcinoma in situ", "shortest_name_length": 25}
{"curie": "MONDO:0019772", "names": ["Meige syndrome", "Meige dystonia", "Meige Syndrome", "meige syndrome", "meiges syndrome", "meige's syndrome", "Meige's syndrome", "Brueghel syndrome", "Brueghel Syndrome", "oral facial dystonia", "Meige syndrome (disorder)", "segmental cranial dystonia", "Idiopathic Orofacial Dyskinesia", "Idiopathic Orofacial Dyskinesias", "Orofacial Dyskinesia, Idiopathic", "Dyskinesia, Idiopathic Orofacial", "Dyskinesias, Idiopathic Orofacial", "Orofacial Dyskinesias, Idiopathic", "Blepharospasm-Oromandibular Dystonia", "Blepharospasm Oromandibular Dystonia", "blepharospasm-oromandibular dystonia", "Dystonia, Blepharospasm-Oromandibular", "Blepharospasm-Oromandibular Dystonias", "Blepharospasm - oromandibular dystonia", "blepharospasm - oromandibular dystonia", "Blepharospasm Oromandibular Dyskinesia", "Dystonias, Blepharospasm-Oromandibular", "Blepharospasm-Oromandibular Dyskinesia", "Blepharospasm-Oromandibular Dyskinesias", "Dyskinesia, Blepharospasm-Oromandibular", "Dyskinesias, Blepharospasm-Oromandibular", "blepharospasm-oromandibular dystonia syndrome", "Blepharospasm-oromandibular dystonia syndrome", "Blepharospasm Oromandibular Dystonia Syndrome", "Blepharospasm-Oromandibular Dystonia Syndrome", "Syndrome, Blepharospasm-Oromandibular Dystonia", "Blepharospasm-Oromandibular Dystonia Syndromes", "Dystonia Syndrome, Blepharospasm-Oromandibular", "Dystonia Syndromes, Blepharospasm-Oromandibular", "Idiopathic Blepharospasm Oromandibular Dystonia Syndrome", "Idiopathic Blepharospasm-Oromandibular Dystonia Syndrome", "idiopathic blepharospasm-oromandibular dystonia syndrome", "Blepharospasm Oromandibular Dystonia Syndrome, Idiopathic", "Blepharospasm-Oromandibular Dystonia Syndrome, Idiopathic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blepharospasm-oromandibular dystonia syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C1334161", "names": ["Immunodeficiency-Related Neoplasm", "Immunosuppression-Related Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immunodeficiency-Related Neoplasm", "shortest_name_length": 33}
{"curie": "UMLS:C0270276", "names": ["Gray syndrome", "grey syndrome", "Grey syndrome", "gray syndrome", "Grey Syndrome", "Gray Syndrome", "gray; syndrome", "syndrome; gray", "gray baby syndrome", "grey baby syndrome", "GRAY BABY SYNDROME", "Gray baby syndrome", "Gray Baby Syndrome", "Grey baby syndrome", "Grey syndrome neonatal", "GRAY SYNDROME NEONATAL", "Gray syndrome neonatal", "GREY SYNDROME NEONATAL", "gray syndrome (newborn)", "Grey syndrome of newborn", "Gray syndrome of newborn", "gray baby syndrome (diagnosis)", "Chloramphenicol toxicity in newborn", "Grey syndrome from chloramphenicol administration in newborn", "Gray syndrome from chloramphenicol administration in newborn", "Gray syndrome from chloramphenicol administration in newborn (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gray syndrome from chloramphenicol administration in newborn", "shortest_name_length": 13}
{"curie": "MONDO:0035525", "names": ["BPES type 2", "blepharophimosis-ptosis-epicanthus inversus syndrome type 2", "blepharophimosis-ptosis-epicanthus inversus syndrome without premature ovarian failure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blepharophimosis-ptosis-epicanthus inversus syndrome type 2", "shortest_name_length": 11}
{"curie": "UMLS:C5237729", "names": ["Recurrent Myelodysplastic/Myeloproliferative Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Myelodysplastic/Myeloproliferative Neoplasm", "shortest_name_length": 53}
{"curie": "MONDO:0044740", "names": ["salivary gland SCC", "Salivary Gland SCC", "SCC of Salivary Gland", "SCC of salivary gland", "SCC of the Salivary Gland", "SCC of the salivary gland", "salivary gland squamous cell cancer", "salivary gland epidermoid carcinoma", "Salivary Gland Epidermoid Carcinoma", "Salivary Gland Squamous Cell Cancer", "epidermoid carcinoma, salivary gland", "epidermoid carcinoma of salivary gland", "Epidermoid Carcinoma of Salivary Gland", "Salivary Gland Squamous Cell Carcinoma", "salivary gland squamous cell carcinoma", "squamous cell carcinoma of salivary gland", "Squamous Cell Carcinoma of Salivary Gland", "squamous cell carcinoma of salivary glands", "Squamous cell carcinoma of salivary glands", "Epidermoid Carcinoma of the Salivary Gland", "epidermoid carcinoma of the salivary gland", "Squamous Cell Carcinoma of the Salivary Gland", "squamous cell carcinoma of the salivary gland", "saliva-secreting gland squamous cell carcinoma", "salivary gland cancer, squamous cell carcinoma", "squamous cell carcinoma of salivary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "salivary gland squamous cell carcinoma", "shortest_name_length": 18}
{"curie": "MONDO:0015867", "names": ["vagina cancer", "Vagina Cancer", "Vaginal Cancer", "vaginal cancer", "Cancer of Vagina", "Vagina Carcinoma", "carcinoma vagina", "vagina carcinoma", "cancer of vagina", "VAGINAL CARCINOMA", "Vaginal Carcinoma", "carcinoma vaginal", "vaginal carcinoma", "Vaginal carcinoma", "carcinoma of vagina", "vaginal cancer, NOS", "Vaginal cancer, NOS", "Carcinoma of vagina", "Carcinoma of Vagina", "cancer of the vagina", "Cancer of the Vagina", "Carcinoma of the Vagina", "carcinoma of the vagina", "Carcinoma of vagina (disorder)", "carcinoma of vagina (diagnosis)", "vaginal malignant epithelial tumor", "Vaginal malignant epithelial tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vaginal carcinoma", "shortest_name_length": 13}
{"curie": "MONDO:0700198", "names": ["Porcine Lymphoma", "porcine lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "porcine lymphoma", "shortest_name_length": 16}
{"curie": "MONDO:0009708", "names": ["MSMB", "congenital myopathy 7B", "autosomal recessive hyaline body myopathy", "Myopathy, Hyaline Body, Autosomal Recessive", "MYOPATHY, HYALINE BODY, AUTOSOMAL RECESSIVE", "myopathy, hyaline body, autosomal recessive", "Myopathy, myosin storage, autosomal recessive", "MYOPATHY, MYOSIN STORAGE, AUTOSOMAL RECESSIVE", "myopathy, myosin storage, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy, myosin storage, autosomal recessive", "shortest_name_length": 4}
{"curie": "MONDO:0011960", "names": ["SCZD11", "Sczd11", "schizophrenia 11", "SCHIZOPHRENIA 11", "schizophrenia type 11", "SCHIZOPHRENIA SUSCEPTIBILITY LOCUS, CHROMOSOME 10q-RELATED", "schizophrenia susceptibility locus, chromosome 10Q-related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schizophrenia 11", "shortest_name_length": 6}
{"curie": "MONDO:0014322", "names": ["Pof9", "POF9", "PREMATURE OVARIAN FAILURE 9", "premature ovarian failure 9", "HFM1 primary ovarian failure", "primary ovarian insufficiency 9", "premature ovarian failure type 9", "primary ovarian failure caused by mutation in HFM1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "premature ovarian failure 9", "shortest_name_length": 4}
{"curie": "MONDO:0008915", "names": ["DCM-HH", "Najjar Syndrome", "Malouf Syndrome", "NAJJAR SYNDROME", "MALOUF SYNDROME", "Najjar syndrome", "Malouf syndrome", "CARDIOGENITAL SYNDROME", "Cardiogenital syndrome", "cardiogenital syndrome", "GENITAL ANOMALY WITH CARDIOMYOPATHY", "Genital Anomaly With Cardiomyopathy", "genital anomaly with cardiomyopathy", "genital anomaly-cardiomyopathy syndrome", "cardiomyopathy with primary testicular failure", "cardiomyopathy eith primary testicular failure", "CARDIOMYOPATHY WITH PRIMARY TESTICULAR FAILURE", "dilated cardiomyopathy with premature ovarian failure", "CARDIOMYOPATHY, DILATED, WITH PREMATURE OVARIAN FAILURE", "cardiomyopathy, dilated, with premature ovarian failure", "dilated cardiomyopathy with hypergonadotropic hypogonadism", "CARDIOMYOPATHY, DILATED, WITH HYPERGONADOTROPIC HYPOGONADISM", "cardiomyopathy, dilated, with hypergonadotropic hypogonadism", "congestive cardiomyopathy with hypergonadotropic hypogonadism", "dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome", "Dilated Cardiomyopathy-Hypergonadotropic Hypogonadism Syndrome", "Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome", "cardiomyopathy, congestive, with hypergonadotropic hypogonadism", "CARDIOMYOPATHY, CONGESTIVE, WITH HYPERGONADOTROPIC HYPOGONADISM", "Cardiomyopathy, Congestive, With Hypergonadotropic Hypogonadism", "Congestive cardiomyopathy-hypergonadotropic hypogonadism syndrome", "congestive cardiomyopathy-hypergonadotropic hypogonadism syndrome", "Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome", "Congestive or dilated cardiomyopathy with hypergonadotropic hypogonadism", "Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0007971", "names": ["Gonzales-del Angel syndrome", "Delayed membranous cranial ossification", "delayed membranous cranial ossification", "membranous cranial ossification, delayed", "Membranous Cranial Ossification, Delayed", "MEMBRANOUS CRANIAL OSSIFICATION, DELAYED", "Delayed membranous cranial ossification (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "delayed membranous cranial ossification", "shortest_name_length": 27}
{"curie": "MONDO:0005165", "names": ["BENIGN TUMOR", "benign tumor", "Benign tumor", "Benign Tumor", "Benign tumour", "benign tumour", "Tumor, benign", "Benign Tumors", "benign tumors", "Tumors, Benign", "Tumour, benign", "benign tumours", "Benign neoplasm", "benign neoplasm", "Benign Neoplasm", "NEOPLASM, BENIGN", "Neoplasm, benign", "Neoplasm, Benign", "Benign neoplasms", "neoplasm, benign", "BENIGN NEOPLASMS", "benign neoplasms", "Benign Neoplasms", "Neoplasms, Benign", "nonmalignant tumor", "Benign neoplasm NOS", "Noncancerous tumors", "NONMALIGNANT TUMORS", "NEOPLASM BENIGN NOS", "nonmalignant tumors", "nonmalignant neoplasm", "Benign tumor morphology", "Benign tumour morphology", "benign neoplasm (disease)", "Benign neoplastic disease", "cell type benign neoplasm", "neoplasm (disease), benign", "Unclassified tumor, benign", "Neoplastic disease, benign", "benign unclassifiable tumor", "Benign Unclassifiable Tumor", "Unclassified tumour, benign", "benign neoplasm (diagnosis)", "organ system benign neoplasm", "Benign tumor or blood disorder", "Neoplasm benign;site unspecifi", "Benign neoplasm, unspecified site", "Benign neoplasm, site unspecified", "Benign neoplasm of unspecified site", "benign neoplasm of unspecified site", "Benign neoplastic disease (disorder)", "Neoplasm, benign (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm", "shortest_name_length": 12}
{"curie": "MONDO:0007390", "names": ["CYPA6*2", "CYP2A6*3", "CYP2A6*11", "CYP2A6*4A", "CYP2A6, V1", "CYP2A6*12A", "CYP2A6, V2", "CYPA6*2 PHENOTYPE", "CYP2A6*3 PHENOTYPE", "COUMARIN RESISTANCE", "warfarin resistance", "Coumarin Resistance", "coumarin resistance", "CYP2A6*4A PHENOTYPE", "Warfarin resistance", "CYP2A6*11 PHENOTYPE", "WARFARIN RESISTANCE", "Warfarin Resistance", "Warfarin Sensitivity", "CYP2A6, V2 PHENOTYPE", "WARFARIN SENSITIVITY", "Warfarin sensitivity", "coumarin sensitivity", "CYP2A6*12A PHENOTYPE", "CYP2A6, V1 PHENOTYPE", "warfarin sensitivity", "Coumarin Sensitivity", "COUMARIN SENSITIVITY", "TEGAFUR, POOR METABOLISM OF", "Coumarin, Poor Metabolism Of", "NICOTINE, POOR METABOLISM OF", "COUMARIN, POOR METABOLISM OF", "coumarin, poor metabolism of", "Warfarin sensitivity (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coumarin resistance", "shortest_name_length": 7}
{"curie": "MONDO:0006223", "names": ["gastric diffuse large B-cell lymphoma", "Gastric Diffuse Large B-Cell Lymphoma", "Primary Diffuse Large B-Cell Gastric Lymphoma", "primary diffuse large B-cell gastric lymphoma", "primary gastric diffuse large B-cell lymphoma", "Primary Gastric Diffuse Large B-Cell Lymphoma", "primary diffuse large B-cell lymphoma of stomach", "Primary Diffuse Large B-Cell Lymphoma of Stomach", "Primary Diffuse Large B-Cell Lymphoma of the Stomach", "primary diffuse large B-cell lymphoma of the stomach"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric diffuse large B-cell lymphoma", "shortest_name_length": 37}
{"curie": "MONDO:0009175", "names": ["EF", "Shulman syndrome", "Shulman Syndrome", "Shulman's syndrome", "shulman's syndrome", "Schulman's syndrome", "EOSINOPHILIC FASCIITIS", "fasciitis eosinophilic", "Eosinophilic fasciitis", "eosinophilic fasciitis", "Eosinophilic Fasciitis", "Fasciitis eosinophilic", "FASCIITIS, EOSINOPHILIC", "eosinophilic fasciitis (disease)", "eosinophilic fasciitis (diagnosis)", "Diffuse fasciitis with eosinophilia", "diffuse fasciitis with eosinophilia", "Fasciitis with eosinophilia syndrome", "eosinophilic fasciitis (Schulman's syndrome)", "Fasciitis with eosinophilia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eosinophilic fasciitis", "shortest_name_length": 2}
{"curie": "UMLS:C5420193", "names": ["Laryngeal Chondroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laryngeal Chondroma", "shortest_name_length": 19}
{"curie": "UMLS:C0854830", "names": ["Stage III T Cell Lymphoma", "Stage III T-Cell Lymphoma", "T-Cell Lymphoma Stage III", "T-cell lymphoma stage III", "T Cell Lymphoma Stage III", "T-cell lymphoma NOS stage III", "Stage III T-Cell Non-Hodgkin Lymphoma", "Stage III T-Cell Non-Hodgkin's Lymphoma", "Ann Arbor Stage III T-Cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-cell lymphoma stage III", "shortest_name_length": 25}
{"curie": "UMLS:C0221480", "names": ["Recurrent Depression", "recurrent depression", "depression recurrent", "Recurrent depression", "recurrent depression (symptom)", "Recurrent depression (disorder)", "recurrent depression (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent depression", "shortest_name_length": 20}
{"curie": "MONDO:0018063", "names": ["WCD", "Weber-Christian", "Christian-Weber", "panniculitis relapsing", "Weber-Kindler syndrome", "Relapsing panniculitis", "relapsing panniculitis", "Weber Christian Disease", "Weber-Christian Disease", "Weber-Christian disease", "weber-christian disease", "WEBER-CHRISTIAN DISEASE", "Weber Christian disease", "christian weber disease", "WEBER CHRISTIAN DISEASE", "weber christian disease", "Disease, Weber-Christian", "disease weber christians", "Weber - Christian disease", "Weber-Christian panniculitis", "Weber Christian panniculitis", "Systemic nodular panniculitis", "Idiopathic lobular panniculitis", "Idiopathic nodular panniculitis", "idiopathic nodular panniculitis", "idiopathic lobular panniculitis", "PFEIFFER-WEBER-CHRISTIAN SYNDROME", "Pfeiffer-Weber-Christian syndrome", "relapsing panniculitis (diagnosis)", "panniculitis nodular nonsuppurative", "nodular nonsuppurative panniculitis", "Nodular Nonsuppurative Panniculitis", "Nonsuppurative Panniculitis, Nodular", "PANNICULITIS, NODULAR NONSUPPURATIVE", "nodular non-suppurative panniculitis", "Panniculitis, Nodular Nonsuppurative", "Nodular non-suppurative panniculitis", "Nodular Nonsuppurative Panniculitides", "Nonsuppurative Panniculitides, Nodular", "Relapsing febrile nodular panniculitis", "Panniculitides, Nodular Nonsuppurative", "Relapsing panniculitis [Weber-Christian]", "Nodular non-suppurative febrile panniculitis", "nodular non-suppurative febrile panniculitis", "Panniculitis, non-suppurative relapsing nodular", "Relapsing febrile nodular nonsuppurative panniculitis", "Relapsing febrile nodular nonsuppurative panniculitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nodular non-suppurative panniculitis", "shortest_name_length": 3}
{"curie": "UMLS:C3661921", "names": ["Perioperative hypertension", "Perioperative hypertension (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perioperative hypertension", "shortest_name_length": 26}
{"curie": "MONDO:0021279", "names": ["submandibular gland mucoepidermoid carcinoma", "Submandibular Gland Mucoepidermoid Carcinoma", "Cancer of submandibular gland, mucoepidermoid", "Mucoepidermoid Carcinoma of Submandibular Gland", "Mucoepidermoid carcinoma of submandibular gland", "mucoepidermoid carcinoma of submandibular gland", "mucoepidermoid carcinoma of the submandibular gland", "Mucoepidermoid Carcinoma of the Submandibular Gland", "Mucoepidermoid carcinoma of submandibular gland (disorder)", "mucoepidermoid carcinoma of submandibular gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucoepidermoid carcinoma of submandibular gland", "shortest_name_length": 44}
{"curie": "EFO:0008532", "names": ["clinically amyopathic dermatomyositis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "clinically amyopathic dermatomyositis", "shortest_name_length": 37}
{"curie": "UMLS:C5420760", "names": ["Conjunctival Reactive Epithelial Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conjunctival Reactive Epithelial Hyperplasia", "shortest_name_length": 44}
{"curie": "MONDO:0008455", "names": ["Segmental spinal muscular atrophy", "SPINAL MUSCULAR ATROPHY, SEGMENTAL", "spinal muscular atrophy, segmental", "Spinal Muscular Atrophy, Segmental"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal muscular atrophy, segmental", "shortest_name_length": 33}
{"curie": "UMLS:C0677730", "names": ["Aggressive Non-Hodgkin Lymphoma", "Aggressive Adult Non-Hodgkin Lymphoma", "aggressive adult non-Hodgkin lymphoma", "aggressive, adult non-Hodgkin lymphoma", "adult aggressive non-Hodgkin's lymphoma", "Adult Aggressive Non-Hodgkin's Lymphoma", "aggressive adult non-Hodgkin's lymphoma", "Aggressive Adult Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aggressive Adult Non-Hodgkin Lymphoma", "shortest_name_length": 31}
{"curie": "UMLS:C1336357", "names": ["Stage IVA Osteosarcoma", "Stage IVA Osteogenic Sarcoma", "Stage IVA Osteosarcoma AJCC v7", "Stage IVA Osteosarcoma  AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Osteosarcoma AJCC v7", "shortest_name_length": 22}
{"curie": "MONDO:0018222", "names": ["X-linked intellectual disability due to GRIA3 anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability due to GRIA3 anomalies", "shortest_name_length": 55}
{"curie": "MONDO:0005605", "names": ["Transitional papilloma", "transitional papilloma", "Transitional Papilloma", "transitional cell papilloma", "Transitional Cell Papilloma", "Transitional cell papilloma", "Transitional cell papilloma NOS", "Transitional cell papilloma, NOS", "PAPILLOMA, UROTHELIAL CELL, BENIGN", "transitional cell papilloma, benign", "Transitional cell papilloma, benign", "papilloma, transitional cell, benign", "transitional cell papilloma NOS (morphologic abnormality)", "Transitional cell papilloma, benign (morphologic abnormality)", "transitional cell papilloma, benign (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transitional cell papilloma", "shortest_name_length": 22}
{"curie": "MONDO:0043982", "names": ["cubital syndrome tunnel", "Cubital Tunnel Syndrome", "Cubital tunnel syndrome", "cubital tunnel syndrome", "Syndrome, Cubital Tunnel", "Tunnel Syndrome, Cubital", "Cubital Tunnel Syndromes", "syndrome, cubital tunnel", "cubital tunnel syndromes", "tunnel syndrome, cubital", "Syndromes, Cubital Tunnel", "tunnel syndromes, cubital", "Tunnel Syndromes, Cubital", "syndromes, cubital tunnel", "ulnar nerve entrapment elbow", "ulnar nerve entrapment, elbow", "Ulnar Nerve Entrapment, Elbow", "Ulnar nerve entrapment at elbow", "cubital tunnel syndrome (diagnosis)", "Ulnar Nerve Compression, Cubital Tunnel", "ulnar nerve compression, cubital tunnel", "Ulnar nerve entrapment at elbow (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cubital tunnel syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0016017", "names": ["MMI/CMZ embryopathy", "MMI/CMZ embryofetopathy", "fetal methimazole syndrome", "methimazole embryofetopathy", "Methimazole embryofetopathy", "Methimazole antenatal exposure", "Methimazole/carbimazole embryopathy", "Embryofetopathy caused by methimazole", "Methimazole/carbimazole embryofetopathy", "Embryofetopathy caused by methimazole (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "methimazole embryofetopathy", "shortest_name_length": 19}
{"curie": "MONDO:0017245", "names": ["congenital intrapulmonary sequestration", "intralobar congenital pulmonary sequestration", "intralobar congenital bronchopulmonary sequestration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intralobar congenital pulmonary sequestration", "shortest_name_length": 39}
{"curie": "UMLS:C0862493", "names": ["Adenocarcinoma endometrial recurrent", "Recurrent Endometrial Adenocarcinoma", "Endometrial adenocarcinoma recurrent", "Endometrioid adenocarcinoma recurrent", "Recurrent Endometrioid Adenocarcinoma", "Recurrent Endometrial Adenocarcinoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma endometrial recurrent", "shortest_name_length": 36}
{"curie": "MONDO:0700110", "names": ["pneumonia, non-human animal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pneumonia, non-human animal", "shortest_name_length": 27}
{"curie": "MONDO:0020326", "names": ["LyP", "LYP", "Lymphomatoid papulosis", "Lymphomatoid Papuloses", "Lymphomatoid Papulosis", "lymphomatoid papulosis", "Papuloses, Lymphomatoid", "papulosis; lymphomatoid", "Papulosis, Lymphomatoid", "Lymphomatoid papulosis (disorder)", "lymphomatoid papulosis (diagnosis)", "Lymphomatoid papulosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphomatoid papulosis", "shortest_name_length": 3}
{"curie": "UMLS:C1514294", "names": ["Pre-pre-B ALL", "Pre-Pre-B Acute Lymphoblastic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pre-Pre-B Acute Lymphoblastic Leukemia", "shortest_name_length": 13}
{"curie": "MONDO:0013265", "names": ["AUTS17", "autism susceptibility 17", "susceptibility to autism 17", "AUTISM, SUSCEPTIBILITY TO, 17", "autism, susceptibility to, 17", "autism, susceptibility to, type 17"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autism, susceptibility to, 17", "shortest_name_length": 6}
{"curie": "MONDO:0023071", "names": ["enterovirus antenatal infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "enterovirus antenatal infection", "shortest_name_length": 31}
{"curie": "MONDO:0013606", "names": ["HPS9", "Hermansky-Pudlak syndrome 9", "HERMANSKY-PUDLAK SYNDROME 9", "Hermansky-Pudlak syndrome type 9", "BLOC1S6 Hermansky-Pudlak syndrome", "Hermansky-Pudlak syndrome caused by mutation in BLOC1S6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hermansky-Pudlak syndrome 9", "shortest_name_length": 4}
{"curie": "MONDO:0007017", "names": ["Detachment;vitreous", "Vitreous detachment", "vitreous detachment", "VITREOUS DETACHMENT", "detachment vitreous", "Vitreous Detachment", "Vitreous separation", "Detachment, Vitreous", "vitreous detachments", "Vitreous Detachments", "Detachments, Vitreous", "eye vitreous detached", "detachment Of vitreous", "vitreous, detachment Of", "post vitreous detachment", "Posterior Vitreous Detachment", "posterior vitreous detachment", "VITREOUS DETACHMENT POSTERIOR", "Posterior vitreous detachment", "Detachment, Posterior Vitreous", "Vitreous detachment (disorder)", "Vitreous Detachment, Posterior", "Posterior Vitreous Detachments", "Posterior Vitreous Detatchment", "Detachments, Posterior Vitreous", "Vitreous Detachments, Posterior", "vitreous detachment (diagnosis)", "PVD - Posterior vitreous detachment", "vitreous detachment (physical finding)", "Posterior vitreous detachment (disorder)", "posterior vitreous detachment (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitreous detachment", "shortest_name_length": 19}
{"curie": "MONDO:0015871", "names": ["BPT", "Phyllodes neoplasm", "phyllodes neoplasm", "cystosarcoma phyllode", "Cystosarcoma phyllodes", "cystosarcoma phylloide", "cystosarcoma phyllodes", "benign phyllodes neoplasm", "benign Phyllodes neoplasm", "phyllode tumor of the breast", "Benign Breast Phyllodes Tumor", "phylloide tumor of the breast", "benign cystosarcoma phyllodes", "benign breast phyllodes tumor", "breast phyllodes tumor, benign", "Benign Phyllodes Tumor of Breast", "Breast Benign Phyllodes Neoplasm", "benign phyllodes tumor of breast", "breast benign phyllodes neoplasm", "cystosarcoma phyllode of the breast", "Benign phyllodes neoplasm of breast", "benign phyllodes neoplasm of breast", "Benign Phyllodes Neoplasm of Breast", "benign phyllodes tumor of the breast", "cystosarcoma phylloide of the breast", "Benign Phyllodes Tumor of the Breast", "Benign Phyllodes Neoplasm of the Breast", "benign Phyllodes neoplasm of the breast", "benign phyllodes neoplasm of the breast", "Benign phyllodes neoplasm of breast (disorder)", "phyllodes tumor, benign (morphologic abnormality)", "cystosarcoma phyllodes NOS (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign breast phyllodes tumor", "shortest_name_length": 3}
{"curie": "MONDO:0032688", "names": ["PMGEDSV", "polymicrogyria with or without vascular-type EDS", "POLYMICROGYRIA WITH OR WITHOUT VASCULAR-TYPE EHLERS-DANLOS SYNDROME", "polymicrogyria with or without vascular-type ehlers-danlos syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polymicrogyria with or without vascular-type ehlers-danlos syndrome", "shortest_name_length": 7}
{"curie": "UMLS:C0265935", "names": ["Congenital anomaly of artery", "Congenital arterial malformation", "Congenital abnormality of artery", "Congenital anomaly of artery, NOS", "Congenital arterial malformation NOS", "CONGENITAL ANOMALIES OF THE ARTERIES", "Congenital arterial malformation, NOS", "Congenital anomaly of artery (diagnosis)", "congenital anomaly of cardiovascular system artery"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital anomaly of artery", "shortest_name_length": 28}
{"curie": "MONDO:0018499", "names": ["DORV with atrioventricular septal defect, pulmonary stenosis, heterotaxy", "double outlet right ventricle with atrioventricular septal defect, pulmonary stenosis, heterotaxy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "double outlet right ventricle with atrioventricular septal defect, pulmonary stenosis, heterotaxy", "shortest_name_length": 72}
{"curie": "UMLS:C0438696", "names": ["SUICIDAL", "suicidal", "Suicidal", "Suicidal (finding)", "suicidal (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Suicidal", "shortest_name_length": 8}
{"curie": "MONDO:0014248", "names": ["AMRS", "SLC35A3-CDG", "arthrogryposis, mental retardation, and seizures", "ARTHROGRYPOSIS, MENTAL RETARDATION, AND SEIZURES", "arthrogryposis, intellectual disability, and seizures", "autism spectrum disorder - epilepsy - arthrogryposis syndrome", "ARTHROGRYPOSIS, IMPAIRED INTELLECTUAL DEVELOPMENT, AND SEIZURES", "arthrogryposis, impaired intellectual development, and seizures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autism spectrum disorder - epilepsy - arthrogryposis syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0011778", "names": ["AGBK", "Mmedf", "MMEDF", "AL-Gazali-BAKALINOVA syndrome", "AL-GAZALI-BAKALINOVA SYNDROME", "Al-Gazali-Bakalinova syndrome", "Multiple epiphyseal dysplasia Al-Gazali type", "multiple epiphyseal dysplasia, Al-Gazali type", "Multiple epiphyseal dysplasia, Al-Gazali type", "Multiple epiphyseal dysplasia Al-Gazali type (disorder)", "macrocephaly with multiple epiphyseal dysplasia and distinctive facies", "multiple epiphyseal dysplasia-macrocephaly-distinctive facies syndrome", "Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies", "MACROCEPHALY WITH MULTIPLE EPIPHYSEAL DYSPLASIA AND DISTINCTIVE FACIES", "Multiple epiphyseal dysplasia-macrocephaly-distinctive facies syndrome", "Multiple epiphyseal dysplasia and macrocephaly with distinctive facies syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple epiphyseal dysplasia, Al-Gazali type", "shortest_name_length": 4}
{"curie": "MONDO:0012152", "names": ["ADHD4", "ATTENTION DEFICIT-HYPERACTIVITY DISORDER, SUSCEPTIBILITY TO, 4", "attention deficit-hyperactivity disorder, susceptibility to, 4", "attention Deficit-hyperactivity disorder, susceptibility to, type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "attention deficit-hyperactivity disorder, susceptibility to, 4", "shortest_name_length": 5}
{"curie": "UMLS:C0332434", "names": ["Stage IV Lymphoma", "stage iv lymphoma", "lymphoma stage iv", "Lymphoma Stage IV", "Lymphoma stage IV", "Ann Arbor Stage IV Lymphoma", "Lymphoma stage IV (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoma stage IV", "shortest_name_length": 17}
{"curie": "UMLS:C3897236", "names": ["Untreated Cerebral Astrocytoma", "untreated childhood cerebral astrocytoma", "Untreated Childhood Cerebral Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Untreated Childhood Cerebral Astrocytoma", "shortest_name_length": 30}
{"curie": "MONDO:0010229", "names": ["ALPC", "Atrichia congenita", "alopecia congenita", "atrichia congenita", "Congenital Alopecia", "congenital alopecia", "Congenital alopecia", "Alopecia congenital", "ALOPECIA, CONGENITAL", "congenital; alopecia", "Alopecia, Congenital", "congenital; atrichia", "atrichia; congenital", "alopecia, congenital", "Alopecia, congenital", "alopecia; congenital", "Congenital atrichosis", "Nevoid congenital alopecia", "Naevoid congenital alopecia", "Congenital alopecia X-linked", "Atrichia congenita (disorder)", "Congenital alopecia (disorder)", "congenital alopecia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alopecia, congenital", "shortest_name_length": 4}
{"curie": "MONDO:0004306", "names": ["childhood conventional osteosarcoma", "Childhood Conventional Osteosarcoma", "childhood intracortical osteosarcoma", "Childhood Intracortical Osteosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood intracortical osteosarcoma", "shortest_name_length": 35}
{"curie": "UMLS:C1336816", "names": ["TCSSC", "Transplant-Related Skin Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transplant-Related Skin Squamous Cell Carcinoma", "shortest_name_length": 5}
{"curie": "UMLS:C5555593", "names": ["Idiopathic Basal Ganglia Calcification"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Idiopathic Basal Ganglia Calcification", "shortest_name_length": 38}
{"curie": "MONDO:0100486", "names": ["adult acne", "ACNE, ADULT", "Acne, Adult", "acne, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult acne", "shortest_name_length": 10}
{"curie": "UMLS:C4524463", "names": ["Metastatic Thyroid Gland Cancer", "Metastatic Thyroid Gland Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Thyroid Gland Carcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C4763896", "names": ["H influenze type B Pneumonia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "H influenze type B Pneumonia", "shortest_name_length": 28}
{"curie": "UMLS:C0862200", "names": ["recurrent mycosis fungoides/Sezary syndrome", "Mycosis fungoides/Sezary syndrome recurrent", "mycosis fungoides/Sezary syndrome, recurrent", "Recurrent Mycosis Fungoides and Sézary Syndrome", "Recurrent Mycosis Fungoides and Sezary Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mycosis fungoides/Sezary syndrome recurrent", "shortest_name_length": 43}
{"curie": "MONDO:0004662", "names": ["Heterophyosis", "heterophyiasis", "HETEROPHYIASIS", "Heterophyiasis", "Heterophyes infection", "infections, Heterophyes", "heterophyiasis (diagnosis)", "Heterophyes infectious disease", "heterophyes infectious disease", "Heterophyes heterophyes infection", "Infection by Heterophyes heterophyes", "Infection caused by Heterophyes heterophyes", "Infection caused by Heterophyes heterophyes (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heterophyiasis", "shortest_name_length": 13}
{"curie": "UMLS:C4725087", "names": ["Recurrent Human Papillomavirus-Related Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Human Papillomavirus-Related Malignant Neoplasm", "shortest_name_length": 57}
{"curie": "UMLS:C0684256", "names": ["Bacterial sepsis", "bacterial sepsis", "sepsis bacterial", "sepsis; bacterial", "bacterial; sepsis", "bacterial septicemia", "Bacterial septicemia", "Bacterial sepsis, NOS", "Bacterial septicaemia", "Bacterial septicemia, NOS", "Bacterial septicaemia, NOS", "Bacterial sepsis (disorder)", "MISCELLANEOUS BACTERIAL SEPTICEMIAS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bacterial sepsis", "shortest_name_length": 16}
{"curie": "MONDO:0015009", "names": ["HFASD", "LMPHM7", "LYMPHATIC MALFORMATION 7", "lymphatic malformation 7", "CENTRAL CONDUCTION LYMPHATIC ANOMALY", "HYDROPS FETALIS, NONIMMUNE, AND/OR ATRIAL SEPTAL DEFECT", "hydrops fetalis, nonimmune, and/or atrial septal defect, susceptibility to", "hydrops fetalis, nonimmune, and/or atrial septal defect, susceptibility to; HFASD"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphatic malformation 7", "shortest_name_length": 5}
{"curie": "UMLS:C0751445", "names": ["poliencephalitis", "Poliencephalitis", "POLIENCEPHALITIS", "POLIOENCEPHALITIS", "Polioencephalitis", "polioencephalitis", "polio encephalitis", "Polio Encephalitis", "Encephalitis, Polio", "Poliomyelitis encephalitis", "Polioencephalitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Encephalitis, Polio", "shortest_name_length": 16}
{"curie": "MONDO:0013856", "names": ["hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, mental retardation, and recurrent inflammatory episodes", "HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITAL ABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES", "hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, intellectual disability, and recurrent inflammatory episodes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, intellectual disability, and recurrent inflammatory episodes", "shortest_name_length": 137}
{"curie": "MONDO:0018027", "names": ["Idic(15)", "idic(15)", "Invdup(15)", "Inv Dup(15)", "Inv dup(15)", "tetrasomy 15q", "idic (15) syndrome", "Inv dup (15) syndrome", "Inverted duplication 15", "Inverted Duplication 15", "inverted duplication 15", "non-distal tetrasomy 15q", "Non-distal tetrasomy 15q", "Non-Distal Tetrasomy 15q", "chromosome 15q tetrasomy", "Isodicentric Chromosome 15", "Isodicentric 15 chromosome", "Duplication/inversion 15q11", "Non-telomeric tetrasomy 15q", "duplication/inversion 15q11", "Duplication-Inversion 15q11", "non-telomeric tetrasomy 15q", "Duplication/inversion type 15q11", "Isodicentric Chromosome 15 Syndrome", "Isodicentric chromosome 15 syndrome", "Inverted duplicated chromosome 15 syndrome", "Isodicentric chromosome 15 syndrome (disorder)", "Isodicentric chromosome 15 syndrome (diagnosis)", "anomaly of chromosome pair isodicentric chromosome 15 syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "duplication/inversion 15q11", "shortest_name_length": 8}
{"curie": "MONDO:0013445", "names": ["C9D", "C9 deficiency", "C9 Deficiency", "C9 DEFICIENCY", "COMPLEMENT COMPONENT 9 DEFICIENCY", "Complement Component 9 Deficiency", "complement component 9 deficiency", "C9 classic complement early component deficiency", "classic complement early component deficiency caused by mutation in C9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complement component 9 deficiency", "shortest_name_length": 3}
{"curie": "MONDO:0014028", "names": ["DA5D", "ECEL1 distal arthrogryposis", "Distal arthrogryposis type 5D", "distal type 5D arthrogryposis", "distal arthrogryposis type 5D", "ARTHROGRYPOSIS, DISTAL, TYPE 5D", "arthrogryposis, distal, type 5D", "DA5D - distal arthrogryposis type 5D", "Distal arthrogryposis type 5D (disorder)", "distal type 5D arthrogryposis (diagnosis)", "distal arthrogryposis caused by mutation in ECEL1", "distal arthrogryposis type 5 without ophthalmoplegia", "Distal arthrogryposis type 5 without ophthalmoplegia", "Distal arthrogryposis type 5 without ophthalmoparesis", "distal arthrogryposis type 5 without ophthalmoparesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal arthrogryposis type 5D", "shortest_name_length": 4}
{"curie": "MONDO:0024285", "names": ["IgE heavy chain disease", "heavy chain disease epsilon", "epsilon-heavy chain disease", "Epsilon heavy chain disease", "Heavy chain disease, IgE type", "Epsilon heavy chain disease (disorder)", "Epsilon heavy chain disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epsilon-heavy chain disease", "shortest_name_length": 23}
{"curie": "UMLS:C4330469", "names": ["Iatrogenic Contrasexual Pubertal Development"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Iatrogenic Contrasexual Pubertal Development", "shortest_name_length": 44}
{"curie": "MONDO:0019698", "names": ["bent bone dysplasia", "Bent bone dysplasia", "campomelic dysplasia and related disorders", "Campomelic dysplasia and related disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bent bone dysplasia", "shortest_name_length": 19}
{"curie": "MONDO:0013886", "names": ["CECBA", "CANPMR", "nonprogressive cerebellar ataxia with mental retardation", "CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION", "cerebellar ataxia, nonprogressive, with mental retardation", "nonprogressive cerebellar atxia with intellectual disability", "nonprogressive cerebellar ataxia with intellectual disability", "non-progressive cerebellar ataxia with intellectual disability", "Non-progressive cerebellar ataxia with intellectual disability", "cerebellar ataxia, nonprogressive, with intellectual disability", "Non-progressive cerebellar ataxia with intellectual disability (disorder)", "non-progressive cerebellar ataxia with intellectual disability (diagnosis)", "cerebellar dysfunction with variable cognitive and behavioral abnormalities", "CEREBELLAR DYSFUNCTION WITH VARIABLE COGNITIVE AND BEHAVIORAL ABNORMALITIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellar dysfunction with variable cognitive and behavioral abnormalities", "shortest_name_length": 5}
{"curie": "MONDO:0005890", "names": ["Big head", "big head", "big heads", "brown tumor", "Brown tumor", "brown tumors", "Brown tumour", "Bran disease", "browns tumor", "brans disease", "osteitis fibrosa", "Fibro-osteoclasia", "OSTEITIS, PARATHYROID", "fibrous osteodystrophy", "Fibrous osteodystrophy", "Osteodystrophia fibrosa", "osteitis cystica fibrosa", "OSTEITIS FIBROSA CYSTICA", "Osteitis fibrosa cystica", "osteitis fibrosa cystica", "Osteitis Fibrosa Cystica", "Recklinghausen Disease, Bone", "von Recklinghausen's in bone", "Recklinghausen; bone disease", "bone disease; Recklinghausen", "ENGEL-RECKLINGHAUSEN SYNDROME", "hyperparathyroid bone disease", "Hyperparathyroid bone disease", "Recklinghausens Disease, Bone", "Recklinghausen Disease of Bone", "RECKLINGHAUSEN DISEASE OF BONES", "Recklinghausen's Disease of Bone", "type I neurofibromatosis in bone", "von Recklinghausen's bone disease", "Von Recklinghausen; disease, bone", "Von Recklinghausen's bone disease", "disease; Von Recklinghausen, bone", "Von Recklinghausen disease of Bone", "Von Recklinghausen Disease of Bone", "Osteitis fibrosa cystica (disorder)", "von Recklinghausen's disease of bone", "Von Recklinghausen's disease of bone", "Von Recklinghausen's Disease of Bone", "Von Recklinghausen's disease of Bone", "OSTEITIS FIBROSA CYSTICA GENERALISATA", "osteitis fibrosa cystica generalisata", "Osteitis fibrosa cystica generalisata", "osteitis; fibrosa, cystica (generalisata)", "fibrosa; osteitis, cystica (generalisata)", "type I neurofibromatosis in bone (diagnosis)", "neurofibromatosis type I (von Recklinghausen's) in bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteitis fibrosa", "shortest_name_length": 8}
{"curie": "MONDO:0005664", "names": ["bartonellosis", "Bartonellosis", "BARTONELLOSIS", "Bartonelloses", "Guaitara fever", "bartonelliasis", "CARRION DISEASE", "carrion's disease", "Carrion's disease", "Bartonella infection", "Bartonella Infection", "Bartonella; infection", "Bartonella infections", "Rochalimaea Infection", "infection; Bartonella", "Rochalimaea infection", "Bartonella Infections", "Infection, Bartonella", "Rochalimaea infections", "Infection, Rochalimaea", "Rochalimaea Infections", "Infections, Bartonella", "Infections, Rochalimaea", "Bartonellosis (disorder)", "Bartonellosis (diagnosis)", "Bartonellosis, unspecified", "Bartonella infectious disease", "Bartonella disease or disorder", "Rochalimaea infection (disorder)", "bartonellosis (Carrion's disease)", "Bartonella caused disease or disorder", "infection by Bartonella bacilliformis (Carrion's disease)", "infection by Bartonella bacilliformis (Carrion's disease) (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bartonellosis", "shortest_name_length": 13}
{"curie": "MONDO:0000723", "names": ["stammer", "stutter", "Stutter", "Stammer", "stutters", "Dysphemia", "stuttered", "STUTTERING", "stuttering", "stammering", "Stammering", "Stuttering", "STAMMERING", "adults stutter", "Stuttering NOS", "stutter disorder", "adult stuttering", "Adult Stuttering", "adults stuttering", "Non-fluent speech", "Stuttering, Adult", "stammering acquired", "Acquired Stuttering", "Acquired stuttering", "Acquired stammering", "Childhood Stuttering", "stuttering (symptom)", "Stuttering, Acquired", "Stuttering (finding)", "Stuttering, Childhood", "stammering (diagnosis)", "Stuttering in children", "stuttering (diagnosis)", "Developmental Stuttering", "speech rhythm stammering", "Stuttering, Developmental", "speech fluency stuttering", "stuttering (physical finding)", "stammering (physical finding)", "Acquired stammering (disorder)", "familial persistent stuttering", "Acquired stammering (diagnosis)", "stuttering, familial persistent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stutter disorder", "shortest_name_length": 7}
{"curie": "UMLS:C5554633", "names": ["Refractory WHO Grade 1 Glioma", "Refractory WHO Grade I Glioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory WHO Grade 1 Glioma", "shortest_name_length": 29}
{"curie": "MONDO:0013516", "names": ["RP60", "RETINITIS PIGMENTOSA 60", "retinitis pigmentosa 60", "PRPF6 retinitis pigmentosa", "retinitis pigmentosa type 60", "retinitis pigmentosa caused by mutation in PRPF6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 60", "shortest_name_length": 4}
{"curie": "UMLS:C5206440", "names": ["Stage IB1 Cervical Cancer FIGO 2018", "Stage IB1 Cervical Carcinoma FIGO 2018"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB1 Cervical Cancer FIGO 2018", "shortest_name_length": 35}
{"curie": "MONDO:0016594", "names": ["superficial siderosis", "superficial siderosis of the CNS", "superficial hemosiderosis of the CNS", "hemosiderosis of the central nervous system", "superficial siderosis of the central nervous system", "superficial hemosiderosis of the central nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "superficial siderosis", "shortest_name_length": 21}
{"curie": "MONDO:0017144", "names": ["alpha-thalassemia and related diseases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alpha-thalassemia and related diseases", "shortest_name_length": 38}
{"curie": "MONDO:0043352", "names": ["fournier disease", "Fournier disease", "Fournier Disease", "fourniers disease", "FOURNIER GANGRENE", "fournier gangrene", "Fournier Gangrene", "Fournier gangrene", "Fourniers Disease", "Fourniers disease", "Fournier; gangrene", "fourniers gangrene", "gangrene; Fournier", "gangrene, Fournier", "Fournier's Disease", "Fourniers Gangrene", "Fournier's disease", "Gangrene, Fournier", "fournier's disease", "Fourniers gangrene", "gangrene fournier's", "fournier's gangrene", "Fournier's gangrene", "Fournier's Gangrene", "Gangrene, Fournier's", "gangrene, Fournier's", "fournier gangrene (diagnosis)", "Fournier's gangrene (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fournier gangrene", "shortest_name_length": 16}
{"curie": "MONDO:0013585", "names": ["HLS2", "HYDROLETHALUS SYNDROME 2", "hydrolethalus syndrome 2", "Hydrolethalus Syndrome 2", "KIF7 hydrolethalus syndrome", "hydrolethalus syndrome type 2", "hydrolethalus syndrome caused by mutation in KIF7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hydrolethalus syndrome 2", "shortest_name_length": 4}
{"curie": "MONDO:0043168", "names": ["Panostotic fibrous dysplasia", "panostotic fibrous dysplasia", "unusual facial appearance, bone fragility, hyperphosphatasemia, and hypophosphatemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "panostotic fibrous dysplasia", "shortest_name_length": 28}
{"curie": "MONDO:0015277", "names": ["MTC", "THME", "C Cell Carcinoma", "C cell carcinoma", "C-Cell Carcinoma", "Medullary carcinoma", "Medullary Carcinoma", "medullary carcinoma", "Medullary Carcinomas", "Carcinoma, Medullary", "Carcinomas, Medullary", "Medullary carcinoma NOS", "Medullary adenocarcinoma", "cancer medullary thyroid", "Medullary Carcinoma, NOS", "THYROID CANCER MEDULLARY", "Medullary thyroid cancer", "Medullary Thyroid Cancer", "medullary thyroid cancer", "Medullary carcinoma, NOS", "thyroid cancer, medullary", "THYROID, CARCINOMA, SOLID", "Thyroid cancer, medullary", "Medullary thyroid carcinoma", "medullary carcinoma thyroid", "thyroid medullary carcinoma", "Thyroid Medullary Carcinoma", "Medullary Thyroid Carcinoma", "THYROID MEDULLARY CARCINOMA", "medullary thyroid carcinoma", "carcinoma medullary thyroid", "thyroid carcinoma, medullary", "carcinoma, C-cell, malignant", "CARCINOMA, C-CELL, MALIGNANT", "carcinomas medullary thyroid", "Thyroid carcinoma, medullary", "THYROID, CARCINOMA, MEDULLARY", "STRUMA, METASTASIZING AMYLOID", "Ultimobranchial thyroid tumor", "ultimobranchial thyroid tumor", "Parafollicular cell carcinoma", "parafollicular cell carcinoma", "Parafollicular Cell Carcinoma", "Thyroid Gland Medullary Cancer", "ultimobranchial thyroid tumour", "thyroid gland medullary cancer", "Medullary carcinoma of thyroid", "medullary carcinoma of thyroid", "Ultimobranchial thyroid tumour", "Medullary Carcinoma of Thyroid", "Medullary thyroid cancer (MTC)", "of medullary carcinoma thyroid", "medullary thyroid cancer (MTC)", "medullary carcinoma (diagnosis)", "solid carcinoma of thyroid gland", "carcinoma of parafollicular cell", "medullary thyroid gland carcinoma", "Medullary Thyroid Gland Carcinoma", "MTC - Medullary thyroid carcinoma", "Thyroid Gland Medullary Carcinoma", "thyroid gland medullary carcinoma", "medullary carcinoma of the thyroid", "Medullary Carcinoma of the Thyroid", "Solid carcinoma with amyloid stroma", "THYROID CANCER, MEDULLARY CARCINOMA", "solid carcinoma of the thyroid gland", "medullary carcinoma of thyroid gland", "C Cell Carcinoma with Amyloid Stroma", "Medullary Carcinoma of Thyroid Gland", "Thyroid Gland Neuroendocrine Carcinoma", "Medullary thyroid carcinoma (disorder)", "thyroid gland neuroendocrine carcinoma", "Medullary Carcinoma with Amyloid Stroma", "Medullary carcinoma with amyloid stroma", "Medullary carcinoma of thyroid syndrome", "medullary thyroid carcinoma (diagnosis)", "Medullary Carcinoma of the Thyroid Gland", "Medullary carcinoma of the Thyroid gland", "Parafollicular cell carcinoma (disorder)", "medullary carcinoma of the thyroid gland", "C Cell Adenocarcinoma with Amyloid Stroma", "Medullary Carcinoma, Not Otherwise Specified", "Medullary Adenocarcinoma with Amyloid Stroma", "Medullary carcinoma (morphologic abnormality)", "medullary thyroid carcinoma with amyloid stroma", "solid carcinoma of the thyroid gland (diagnosis)", "Parafollicular Cell Carcinoma with Amyloid Stroma", "medullary carcinoma of thyroid with amyloid stroma", "Thyroid Gland Medullary Carcinoma with Amyloid Stroma", "Medullary Thyroid Gland Carcinoma with Amyloid Stroma", "Parafollicular Cell Adenocarcinoma with Amyloid Stroma", "medullary carcinoma of thyroid gland with amyloid stroma", "medullary; carcinoma with amyloid stroma, unspecified site", "carcinoma; medullary with amyloid stroma, unspecified site", "medullary thyroid carcinoma with amyloid stroma (diagnosis)", "Medullary carcinoma with amyloid stroma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "medullary thyroid gland carcinoma", "shortest_name_length": 3}
{"curie": "UMLS:C1336477", "names": ["Stage I Renal Pelvis Cancer", "Stage I Renal Pelvis Carcinoma", "Stage I Carcinoma of Renal Pelvis", "Stage I Renal Pelvis Cancer AJCC v7", "Stage I Carcinoma of the Renal Pelvis", "Stage I Renal Pelvis Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Renal Pelvis Cancer AJCC v7", "shortest_name_length": 27}
{"curie": "UMLS:C2347539", "names": ["Adult Acute Myeloid Leukemia with Recurrent Genetic Abnormalities", "Acute Myeloid Leukemia (AML) with Recurrent Genetic Abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Acute Myeloid Leukemia with Recurrent Genetic Abnormalities", "shortest_name_length": 65}
{"curie": "MONDO:0007942", "names": ["Mammastatin", "MAMMASTATIN", "mammastatin", "MAMMASTATIN PHENOTYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mammastatin", "shortest_name_length": 11}
{"curie": "MONDO:0021559", "names": ["nonautoimmune hemolytic anemia", "non-autoimmune hemolytic anemia", "Non-Autoimmune Hemolytic Anemia", "Non-autoimmune hemolytic anemia", "anemia; hemolytic, nonautoimmune", "Non-autoimmune hemolytic anemias", "hemolytic; anemia, nonautoimmune", "Non-autoimmune haemolytic anaemia", "drug; nonautoimmune hemolytic anemia", "non-autoimmune acquired hemolytic anemia", "Non-autoimmune hemolytic anemia (disorder)", "anemia; hemolytic, acquired, nonautoimmune", "hemolytic; anemia, acquired, nonautoimmune", "non-autoimmune hemolytic anemia (diagnosis)", "Non-autoimmune hemolytic anemia, unspecified", "disease (or disorder); nonautoimmune hemolytic", "Non-autoimmune haemolytic anaemia, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-autoimmune hemolytic anemia", "shortest_name_length": 30}
{"curie": "MONDO:0032762", "names": ["DFNB115", "autosomal recessive deafness 115", "DEAFNESS, AUTOSOMAL RECESSIVE 115", "deafness, autosomal recessive 115", "hearing loss, autosomal recessive 115", "autosomal recessive nonsyndromic deafness 115"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal recessive 115", "shortest_name_length": 7}
{"curie": "MONDO:0007121", "names": ["aniridia, microcornea, and spontaneously Reabsorbed cataract", "Aniridia, Microcornea, And Spontaneously Reabsorbed Cataract", "ANIRIDIA, MICROCORNEA, AND SPONTANEOUSLY REABSORBED CATARACT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aniridia, microcornea, and spontaneously Reabsorbed cataract", "shortest_name_length": 60}
{"curie": "MONDO:0003889", "names": ["Clear cell (glycogen-rich) urothelial carcinoma", "clear cell variant infiltrating bladder urothelial carcinoma", "Infiltrating Bladder Urothelial Carcinoma, Clear Cell Variant", "infiltrating bladder urothelial carcinoma, clear cell variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infiltrating bladder urothelial carcinoma, clear cell variant", "shortest_name_length": 47}
{"curie": "DOID:4548", "names": ["mesenchymal extraosseous chondrosarcoma", "Mesenchymal Extraosseous Chondrosarcoma", "extraskeletal mesenchymal chondrosarcoma", "Extraskeletal Mesenchymal Chondrosarcoma", "Mesenchymal Extraskeletal Chondrosarcoma", "Extraskeletal mesenchymal chondrosarcoma", "Extraskeletal mesenchymal chondrosarcoma (disorder)", "Extraskeletal mesenchymal chondrosarcoma (diagnosis)", "malignant neoplasm chondrosarcoma extraskeletal mesenchymal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extraskeletal mesenchymal chondrosarcoma", "shortest_name_length": 39}
{"curie": "MONDO:0019964", "names": ["thymus NET", "thymic neuroendocrine tumor", "thymus neuroendocrine tumor", "thymus neuroendocrine neoplasm", "neuroendocrine neoplasm of thymus", "thymus neuroendocrine tumor, well differentiated, low or intermediate grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thymic neuroendocrine tumor", "shortest_name_length": 10}
{"curie": "UMLS:C4304383", "names": ["Influenza caused by pandemic influenza virus", "Influenza caused by pandemic influenza virus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Influenza caused by pandemic influenza virus", "shortest_name_length": 44}
{"curie": "MONDO:0006093", "names": ["ascending colon NET G1", "Ascending Colon NET G1", "ascending colon carcinoid tumor", "Ascending Colon Carcinoid Tumor", "Carcinoid Tumor of Ascending Colon", "carcinoid tumor of ascending colon", "carcinoid tumor of the ascending colon", "Carcinoid Tumor of the Ascending Colon", "ascending colon neuroendocrine tumor G1", "Ascending Colon Neuroendocrine Tumor G1", "ascending colon carcinoid tumor (disease)", "ascending colon neuroendocrine neoplasm G1", "grade 1 neuroendocrine neoplasm of ascending colon", "ascending colon neuroendocrine tumor, well differentiated, low grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ascending colon neuroendocrine tumor G1", "shortest_name_length": 22}
{"curie": "MONDO:0017634", "names": ["Non-infectious iridocyclitis", "non-infectious iridocyclitis", "non-infectious anterior uveitis", "Non-infectious anterior uveitis", "non-infectious anterior iridocyclitis", "iridocyclitis non-infectious anterior", "Non-infectious anterior uveitis (disorder)", "non-infectious anterior iridocyclitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-infectious anterior uveitis", "shortest_name_length": 28}
{"curie": "MONDO:0000462", "names": ["eye adnexa disease", "eye adnexa disorder", "ocular adnexa disease", "ocular adnexa disorder", "disease of ocular adnexa", "Disorder of ocular adnexa", "disorder of ocular adnexa", "ocular adnexa disease or disorder", "ocular adnexa disorder (diagnosis)", "Disorder of ocular adnexa (disorder)", "disease or disorder of ocular adnexa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eye adnexa disorder", "shortest_name_length": 18}
{"curie": "UMLS:C0406378", "names": ["Oral erosive lichen", "Erosive oral lichen planus", "erosive oral lichen planus", "Erosive oral lichen planus (disorder)", "erosive oral lichen planus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Erosive oral lichen planus", "shortest_name_length": 19}
{"curie": "UMLS:C4329646", "names": ["Cerebellar, Brain Stem, and Cervical Spinal Cord Ependymal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebellar, Brain Stem, and Cervical Spinal Cord Ependymal Tumor", "shortest_name_length": 64}
{"curie": "MONDO:0017623", "names": ["PHTS", "PTEN HAMARTOMA TUMOR SYNDROME", "PTEN hamartoma tumor syndrome", "PTEN Hamartoma Tumor Syndrome", "PTEN hamartoma tumour syndrome", "PTEN hamartoma tumor syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PTEN hamartoma tumor syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0581395", "names": ["PENIS INFECTION", "penis infection", "infection penis", "penile infection", "penis; infection", "Penile infection", "infection penile", "infections penis", "Penile Infection", "infection; penis", "infections penile", "infection of penis", "Infection of penis", "Penile infection NOS", "Penile infection (diagnosis)", "Infection of penis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Penile Infection", "shortest_name_length": 15}
{"curie": "EFO:1001930", "names": ["idiopathic osteonecrosis of the femoral head"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic osteonecrosis of the femoral head", "shortest_name_length": 44}
{"curie": "UMLS:C5419873", "names": ["Pancreatic Undifferentiated Rhabdoid Carcinoma", "Pancreatic Undifferentiated Carcinoma with Rhabdoid Cells"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Undifferentiated Carcinoma with Rhabdoid Cells", "shortest_name_length": 46}
{"curie": "MONDO:0002442", "names": ["LQT", "Long QT syndrome", "long QT syndrome", "long qt syndrome", "Long QT Syndrome", "LONG QT SYNDROME", "long Q-T syndrome", "Long Q-T syndrome", "long q-t syndrome", "long q t syndrome", "Romano-Ward syndrome", "Long QT syndrome, NOS", "Long QT syndrome (disorder)", "long QT syndrome (diagnosis)", "Prolonged Q-T interval syndrome", "Prolonged Q-T interval syndrome, NOS", "Ventricular arrhythmia associated with long QT syndrome", "ventricular arrhythmia associated with long QT syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "long QT syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0002467", "names": ["Labyrinthitis", "labyrinthitis", "disease inner ear", "inner ear disease", "Labyrinth Disease", "disease ear inner", "Inner Ear Disease", "labyrinth disease", "Disorder;labyrinth", "inner ear diseases", "labyrinth disorder", "Ear Disease, Inner", "inner ear disorder", "Inner ear disorder", "Inner Ear Diseases", "diseases ear inner", "Inner Ear Disorder", "Labyrinth Diseases", "diseases inner ear", "inner Ear disorder", "Ear Diseases, Inner", "vestibular disorder", "Labyrinth Disorders", "Inner Ear Infection", "inner ear disorders", "disorders ear inner", "Vestibular Disorder", "Vestibular disorder", "Labyrinthine vertigo", "labyrinthine disease", "VERTIGO LABYRINTHINE", "Vertigo labyrinthine", "internal ear disease", "internal Ear disorder", "diseases of inner ear", "Disorder of inner ear", "Labyrinthine disorder", "Internal Ear Disorder", "labyrinthine disorder", "DISORDER LABYRINTHINE", "Diseases of inner ear", "disorder of inner ear", "labyrinthine; vertigo", "Vertigo, labyrinthine", "Disorder labyrinthine", "LABYRINTHINE DISORDER", "vertigo; labyrinthine", "Internal Ear Infection", "Labyrinthine disorders", "LABYRINTHINE DISORDERS", "labyrinthine disorders", "Inner ear disorder NOS", "disease of internal ear", "disorder of labyrinthine", "disorder of internal ear", "Labyrinthine disorder NOS", "Infectious Otitis Interna", "Labyrinthine disorder, NOS", "Diseases of inner ear (H80-H83)", "Labyrinthine disorder (disorder)", "disease (or disorder); inner ear", "internal ear disease or disorder", "Disorder of inner ear (disorder)", "Unspecified disease of inner ear", "Disease of inner ear, unspecified", "disorder of inner ear (diagnosis)", "labyrinthine disorders (diagnosis)", "disease or disorder of internal ear", "Unspecified disease of inner ear, unspecified ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inner ear disorder", "shortest_name_length": 13}
{"curie": "MONDO:0024665", "names": ["gynandrism", "indeterminate sex and/or pseudohermaphroditism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "indeterminate sex and/or pseudohermaphroditism", "shortest_name_length": 10}
{"curie": "MONDO:0001640", "names": ["Gonococcal spondylitis", "gonococcal spondylitis", "Gonococcal spondylitis (disorder)", "gonococcal spondylitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gonococcal spondylitis", "shortest_name_length": 22}
{"curie": "MONDO:0021957", "names": ["Congenital nuclear cataract, autosomal recessive", "congenital nuclear cataract, autosomal recessive", "Autosomal recessive nonsyndromic congenital nuclear cataract", "autosomal recessive nonsyndromic congenital nuclear cataract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic congenital nuclear cataract", "shortest_name_length": 48}
{"curie": "MONDO:0022608", "names": ["brittle bone syndrome lethal type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brittle bone syndrome lethal type", "shortest_name_length": 33}
{"curie": "MONDO:0004742", "names": ["spinocerebellar disease", "Spinocerebellar Disease", "Spinocerebellar disease", "SPINOCEREBELLAR DISEASES", "Spinocerebellar Diseases", "Spinocerebellar disorder", "spinocerebellar disorder", "Spinocerebellar disorder NOS", "Spinocerebellar degeneration", "Spinocerebellar disease, NOS", "Spinocerebellar Degeneration", "spinocerebellar degeneration", "SPINOCEREBELLAR DEGENERATION", "spinocerebellar degenerations", "Degeneration, Spinocerebellar", "spino-cerebellar degeneration", "Spinocerebellar Degenerations", "Spino Cerebellar Degeneration", "Spino-Cerebellar Degeneration", "spino cerebellar degeneration", "Degeneration, Spino Cerebellar", "Degeneration, Spino-Cerebellar", "Spino Cerebellar Degenerations", "Degenerations, Spinocerebellar", "Spino-Cerebellar Degenerations", "Primary Cerebellar Degeneration", "Primary cerebellar degeneration", "Degenerations, Spino Cerebellar", "PRIMARY CEREBELLAR DEGENERATION", "primary cerebellar degeneration", "Cerebellar Degeneration, Primary", "Primary Cerebellar Degenerations", "Degeneration, Primary Cerebellar", "Cerebellar Degenerations, Primary", "Degenerations, Primary Cerebellar", "Spinocerebellar disease (disorder)", "Unspecified spinocerebellar disease", "Primary cerebellar degeneration NOS", "Primary cerebellar degeneration, NOS", "Spinocerebellar disease, unspecified", "Primary cerebellar degeneration (disorder)", "primary cerebellar degeneration (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary cerebellar degeneration", "shortest_name_length": 23}
{"curie": "MONDO:0001481", "names": ["FEMUR THROMBOPHLEBITIS", "THROMBOPHLEBITIS, FEMORAL", "thrombophlebitis; femoral", "femoral; thrombophlebitis", "femoral vein thrombophlebitis", "FEMORAL VEIN THROMBOPHLEBITIS", "thrombophlebitis of femoral vein", "Thrombophlebitis of the femoral vein", "thrombophlebitis of the femoral vein", "Thrombophlebitis of deep femoral vein", "thrombophlebitis of deep femoral vein", "thrombophlebitis of femoral vein (diagnosis)", "phlebitis and thrombophlebitis of femoral vein", "Phlebitis and thrombophlebitis of femoral vein", "Thrombophlebitis of the femoral vein (disorder)", "Thrombophlebitis of deep femoral vein (disorder)", "Phlebitis and thrombophlebitis of deep femoral vein", "Phlebitis and thrombophlebitis of femoral vein (deep) (superficial)", "phlebitis and thrombophlebitis of femoral vein (deep) (superficial)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "femoral vein thrombophlebitis", "shortest_name_length": 22}
{"curie": "UMLS:C1520090", "names": ["Vulvar Melanocytic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Melanocytic Neoplasm", "shortest_name_length": 27}
{"curie": "MONDO:0021493", "names": ["Benign Minor Salivary Gland Tumor", "benign minor salivary gland tumor", "benign tumor of minor salivary gland", "Benign Minor Salivary Gland Neoplasm", "benign minor salivary gland neoplasm", "minor salivary gland benign neoplasm", "Benign tumor of minor salivary gland", "Benign Tumor of Minor Salivary Gland", "Benign tumour of minor salivary gland", "benign neoplasm of minor salivary gland", "Benign neoplasm of minor salivary gland", "Benign Neoplasm of Minor Salivary Gland", "Benign Tumor of the Minor Salivary Gland", "benign tumor of the minor salivary gland", "Benign neoplasm of minor salivary gland NOS", "benign neoplasm of the minor salivary gland", "Benign Neoplasm of the Minor Salivary Gland", "Benign neoplasm of minor salivary gland (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of minor salivary gland", "shortest_name_length": 33}
{"curie": "UMLS:C0086743", "names": ["kaschin-beck disease", "Osteoarthritis deformans", "osteoarthritis deformans", "Osteoarthrosis deformans", "Osteoarthrosis Deformans", "Osteoarthritis deformans (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Osteoarthrosis Deformans", "shortest_name_length": 20}
{"curie": "MONDO:0007718", "names": ["familial hepatic adenoma", "hepatic adenoma, somatic", "HEPATIC ADENOMAS, FAMILIAL", "Hepatic Adenomas, Familial", "hepatic adenomas, familial", "familial liver cell adenomas", "LIVER CELL ADENOMAS, FAMILIAL", "Liver Cell Adenomas, Familial", "liver cell adenomas, familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatic adenomas, familial", "shortest_name_length": 24}
{"curie": "MONDO:0004323", "names": ["amyotrophy", "AMYOTROPHY", "Amyotrophy", "amyotrophia", "Amyotrophia", "amyotrophies", "loss; muscle", "muscle; loss", "Muscle atrophy", "Amyotrophy NOS", "ATROPHY MUSCLE", "Atrophy muscle", "MUSCLE ATROPHY", "Muscle Wasting", "muscle atrophy", "Muscle Atrophy", "Muscle wasting", "muscle wasting", "MUSCLE WASTING", "muscle; atrophy", "Muscle thinning", "atrophy; muscle", "Amyotrophia NOS", "Atrophy, Muscle", "Amyotrophy, NOS", "wasting - muscle", "Muscular atrophy", "Amyotrophia, NOS", "muscular atrophy", "Atrophy;muscular", "Muscular Atrophy", "Wasting - muscle", "Muscle Atrophies", "Atrophies, Muscle", "Atrophy, Muscular", "Wasting;muscle(s)", "Muscle hypotrophy", "Atrophy (Muscular)", "muscular atrophies", "Muscular Atrophies", "Muscle wasting, NOS", "DEGENERATION MUSCLE", "Atrophies, Muscular", "Muscle degeneration", "degeneration muscle", "Degeneration muscle", "muscle degeneration", "Muscle atrophy, NOS", "MUSCLE DEGENERATION", "muscle; degeneration", "degeneration; muscle", "Muscular atrophy, NOS", "Muscle wasting disorder", "Atrophy skeletal muscle", "Skeletal muscle atrophy", "skeletal muscle atrophy", "muscle atrophy was seen", "ATROPHY SKELETAL MUSCLE", "Muscle atrophy (disorder)", "Neurogenic muscle atrophy", "Muscle atrophy, neurogenic", "Denervation atrophy, muscle", "Neurogenic Muscular Atrophy", "Neurogenic muscular atrophy", "neurogenic muscular atrophy", "muscular atrophy (diagnosis)", "Muscular atrophy, neurogenic", "Muscular Atrophy, Neurogenic", "Atrophy, Neurogenic Muscular", "Neurotrophic Muscular Atrophy", "Neurogenic Muscular Atrophies", "Denervation atrophy of muscle", "Atrophy, Neurotrophic Muscular", "Atrophies, Neurogenic Muscular", "Group atrophy of muscle fibers", "Muscular Atrophies, Neurogenic", "Muscular Atrophy, Neurotrophic", "Group atrophy of muscle fibres", "Atrophy of the skeletal muscles", "Neurotrophic Muscular Atrophies", "Muscular Atrophies, Neurotrophic", "Atrophies, Neurotrophic Muscular", "muscle atrophy (physical finding)", "Amyotrophy involving the extremities", "Denervation atrophy of muscle (disorder)", "Neurogenic muscle atrophy, especially in the lower limbs"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular atrophy", "shortest_name_length": 10}
{"curie": "MONDO:0014135", "names": ["PPH3", "PULMONARY HYPERTENSION, PRIMARY, 3", "pulmonary hypertension, primary, 3", "CAV1 primary pulmonary hypertension", "pulmonary hypertension, primary, type 3", "primary pulmonary hypertension caused by mutation in CAV1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary hypertension, primary, 3", "shortest_name_length": 4}
{"curie": "MONDO:0004940", "names": ["Female acute pelvic peritonitis", "Acute female pelvic peritonitis", "acute female pelvic peritonitis", "peritonitis; pelvic, female, acute", "acute female pelvic peritonitis (diagnosis)", "Acute or unspecified pelvic peritonitis, female"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute female pelvic peritonitis", "shortest_name_length": 31}
{"curie": "UMLS:C0521794", "names": ["Ectopic growth hormone secretion", "Ectopic Growth Hormone Secretion", "Ectopic Growth Hormone Secretion Syndrome", "Ectopic growth hormone secretion (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ectopic growth hormone secretion", "shortest_name_length": 32}
{"curie": "MONDO:0009495", "names": ["KTLS", "KEUTEL SYNDROME", "KEUTEL syndrome", "Keutel syndrome", "Keutel syndrome (disorder)", "pulmonic stenosis brachytelephalangism and calcification of cartilages", "Pulmonic stenosis, brachytelephalangism, and calcification of cartilages", "pulmonic stenosis, brachytelephalangism, and calcification of cartilages", "PULMONIC STENOSIS, BRACHYTELEPHALANGISM, AND CALCIFICATION OF CARTILAGES", "Pulmonic stenosis-brachytelephalangism-calcification of cartilages syndrome", "pulmonic stenosis-brachytelephalangism-calcification of cartilages syndrome", "Pulmonic stenosis, brachytelephalangism, calcification of cartilage syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Keutel syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0002913", "names": ["Cerebellar Tumor", "cerebellar tumor", "tumor cerebellar", "Cerebellar tumor", "cerebellum tumor", "cerebellar tumors", "Cerebellar Tumors", "Cerebellar tumour", "cerebellum cancer", "cerebellar cancer", "Tumor, Cerebellar", "cerebellar neoplasm", "cerebellum neoplasm", "Tumor of Cerebellum", "Cerebellar Neoplasm", "tumor of cerebellum", "Neoplasm, Cerebellar", "Cerebellar Neoplasms", "Cerebellar tumor NOS", "Cerebellar tumour NOS", "Neoplasms, Cerebellar", "Neoplasm of Cerebellum", "neoplasm of cerebellum", "Neoplasm of cerebellum", "Tumor of the Cerebellum", "tumor of the cerebellum", "Neoplasm of the Cerebellum", "neoplasm of the cerebellum", "cerebellum neoplasm (disease)", "malignant tumor of cerebellum", "malignant tumor of Cerebellum", "Neoplasm of cerebellum (disorder)", "neoplasm of cerebellum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellar neoplasm", "shortest_name_length": 16}
{"curie": "MONDO:0002960", "names": ["polyradiculopathy", "Polyradiculopathy", "Polyradiculopathies", "polyradiculopathies", "Polyradiculopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyradiculopathy", "shortest_name_length": 17}
{"curie": "UMLS:C4683687", "names": ["Noncutaneous Anaplastic Large Cell Lymphoma by Ann Arbor Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Noncutaneous Anaplastic Large Cell Lymphoma by Ann Arbor Stage", "shortest_name_length": 62}
{"curie": "UMLS:C3898654", "names": ["TYPE 4B MYOCARDIAL INFARCTION", "Myocardial infarction type 4b", "Joint Task Force Type 4B Myocardial Infarction", "Joint ESC/ACCF/AHA/WHF Task Force Type 4B Myocardial Infarction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joint Task Force Type 4B Myocardial Infarction", "shortest_name_length": 29}
{"curie": "UMLS:C1519503", "names": ["Stage 0 Renal Pelvis and Ureter Cancer", "Stage 0 Renal Pelvis and Ureter Cancer AJCC v7", "Stage 0 Renal Pelvis and Ureter Urothelial Carcinoma", "Stage 0 Renal Pelvis and Ureter Transitional Cell Carcinoma", "Stage 0 Renal Pelvis and Ureter Urothelial Carcinoma AJCC v7", "stage 0 transitional cell carcinoma in situ of the renal pelvis and ureter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Renal Pelvis and Ureter Cancer AJCC v7", "shortest_name_length": 38}
{"curie": "MONDO:0005640", "names": ["vigil coma", "Coma vigil", "coma vigil", "Coma Vigil", "Coma, vigil", "Vigil, Coma", "Vigils, Coma", "Coma Vigilans", "Coma vigilans", "Akinetic Autism", "akinetic mutism", "Akinetic Mutism", "Akinetic autism", "Agrypnodal coma", "AKINETIC MUTISM", "Akinetic mutism", "mutism akinetic", "Autism, Akinetic", "Akinetic Mutisms", "Mutism, Akinetic", "akinetic; mutism", "Coma vigilans (finding)", "Akinetic mutism (disorder)", "Akinetic mutism (diagnosis)", "disorder speech and language neurologic voice akinetic mutism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "akinetic mutism", "shortest_name_length": 10}
{"curie": "MONDO:0018957", "names": ["Pudendalgia", "pudendal algia", "Pudendal algia", "Alcock syndrome", "pudendal neuralgia", "Pudendal neuralgia", "Pudendal Neuralgia", "Pudendal Neuropathy", "Pudendal Neuralgias", "Neuralgia, Pudendal", "Neuropathy, Pudendal", "Neuralgias, Pudendal", "Pudendal Neuropathies", "Neuropathies, Pudendal", "pudendal nerve neuralgia", "Pudendal Nerve Entrapment", "Nerve Entrapment, Pudendal", "Pudendal Nerve Entrapments", "Entrapment, Pudendal Nerve", "Entrapments, Pudendal Nerve", "neuralgia of pudendal nerve", "Nerve Entrapments, Pudendal", "Pudendal neuralgia (finding)", "Pudendal Canal Entrapment Syndrome", "Pudendal nerve entrapment syndrome", "pudendal nerve entrapment syndrome", "Pudendal Nerve Entrapment Syndrome", "Pudendal neuralgia by pudendal nerve entrapment", "pudendal neuralgia by pudendal nerve entrapment"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pudendal neuralgia", "shortest_name_length": 11}
{"curie": "MONDO:0011411", "names": ["CMCS", "DFNB82, FORMERLY", "Chudley McCullough syndrome", "CHUDLEY-MCCULLOUGH SYNDROME", "Chudley-McCullough syndrome", "Chudley-Mccullough syndrome", "deafness, autosomal recessive 82", "Chudley McCullough syndrome (disorder)", "deafness, autosomal recessive 82, formerly", "DEAFNESS, AUTOSOMAL RECESSIVE 82, FORMERLY", "deafness, bilateral sensorineural, and hydrocephalus due to foramen of Monro obstruction", "Deafness, bilateral sensorineural, and hydrocephalus due to foramen of monro obstruction", "DEAFNESS, SENSORINEURAL, WITH PARTIAL AGENESIS OF THE CORPUS CALLOSUM AND ARACHNOID CYSTS", "Deafness, sensorineural, with partial agenesis of the corpus callosum and arachnoid cysts", "deafness, sensorineural, with partial agenesis of the corpus callosum and arachnoid cysts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chudley-McCullough syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C4763645", "names": ["Relapsed Monomorphic Post-Transplant Lymphoproliferative Disorder", "Recurrent Monomorphic Post-Transplant Lymphoproliferative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Monomorphic Post-Transplant Lymphoproliferative Disorder", "shortest_name_length": 65}
{"curie": "MONDO:0800125", "names": ["disseminated visceral giant cell angiitis", "disseminated visceral giant cell arteritis", "disseminated visceral giant cell arteristic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disseminated visceral giant cell angiitis", "shortest_name_length": 41}
{"curie": "MONDO:0700151", "names": ["canine glioma", "Canine Glioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canine glioma", "shortest_name_length": 13}
{"curie": "MONDO:0012158", "names": ["KTCN2", "keratoconus 2", "KERATOCONUS 2", "Keratoconus 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratoconus 2", "shortest_name_length": 5}
{"curie": "MONDO:0100113", "names": ["hearing loss with skin disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss with skin disease", "shortest_name_length": 30}
{"curie": "UMLS:C5206859", "names": ["Metastatic Sinonasal Squamous Cell Carcinoma", "Metastatic Nasal Cavity and Paranasal Sinus Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Sinonasal Squamous Cell Carcinoma", "shortest_name_length": 44}
{"curie": "UMLS:C0266312", "names": ["Microcystic renal disease", "Microcystic Renal Disease", "Microcystic renal disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Microcystic renal disease", "shortest_name_length": 25}
{"curie": "UMLS:C3640089", "names": ["Respiratory Failure due to Neuromuscular Disorder", "Respiratory Failure Related to Neuromuscular Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Respiratory Failure Related to Neuromuscular Disorder", "shortest_name_length": 49}
{"curie": "UMLS:C5418580", "names": ["Skin Angiolipoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin Angiolipoma", "shortest_name_length": 16}
{"curie": "MONDO:0011464", "names": ["SCA11", "spinocerebellar ataxia 11", "Spinocerebellar Ataxia 11", "SPINOCEREBELLAR ATAXIA 11", "Spinocerebellar ataxia type 11", "spinocerebellar ataxia type 11", "SCA 11 Spinocerebellar Ataxia 11", "Spinocerebellar ataxia type 11 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia type 11", "shortest_name_length": 5}
{"curie": "OMIM:618079", "names": ["LDLCQ8", "LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 6}
{"curie": "UMLS:C0235887", "names": ["Sclerosing peritonitis", "Sclerosing Peritonitis", "PERITONITIS SCLEROSING", "Peritonitis sclerosing", "Sclerosing peritonitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sclerosing peritonitis", "shortest_name_length": 22}
{"curie": "UMLS:C1959797", "names": ["Allergic hepatitis", "Allergic hepatitis (disorder)", "Drug induced immunoallergic hepatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Allergic hepatitis", "shortest_name_length": 18}
{"curie": "UMLS:C2987191", "names": ["Gastric foveolar", "Pancreatic Intraductal Papillary Mucinous Neoplasm, Gastric-Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Intraductal Papillary Mucinous Neoplasm, Gastric-Type", "shortest_name_length": 16}
{"curie": "UMLS:C1970386", "names": ["Cataract, Posterior Polar, 4, With Microphthalmia And Neurodevelopmental Abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cataract, Posterior Polar, 4, With Microphthalmia And Neurodevelopmental Abnormalities", "shortest_name_length": 86}
{"curie": "UMLS:C0234303", "names": ["Secondary Taste Disorder", "Secondary taste disorder", "Taste Disorder, Secondary", "Taste disorder, secondary", "Secondary Taste Disorders", "Taste Disorders, Secondary", "Secondary taste disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Taste Disorder, Secondary", "shortest_name_length": 24}
{"curie": "MONDO:0015057", "names": ["RAE", "AEACEI", "Raas-blocker-induced angioedema", "Reactive angioendotheliomatosis", "reactive angioendotheliomatosis", "Raas-blocker-induced angioneurotic edema", "susceptibility to angioedema induced by ace inhibitors", "angioedema induced by ACE inhibitors, susceptibility to", "Reactive angioendotheliomatosis (morphologic abnormality)", "Angioedema due to angiotensin-converting-enzyme inhibitor", "Angio-oedema due to angiotensin-converting-enzyme inhibitor", "Angioedema caused by angiotensin-converting-enzyme inhibitor", "Angio-oedema caused by angiotensin-converting-enzyme inhibitor", "renin-angiotensin-aldosterone system-blocker-induced angioedema", "Angioedema caused by angiotensin-converting-enzyme inhibitor (disorder)", "renin-angiotensin-aldosterone system-blocker-induced angioneurotic edema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renin-angiotensin-aldosterone system-blocker-induced angioedema", "shortest_name_length": 3}
{"curie": "MONDO:0017101", "names": ["FCD type IIa", "isolated focal cortical dysplasia type IIa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated focal cortical dysplasia type IIa", "shortest_name_length": 12}
{"curie": "MONDO:0012391", "names": ["EPMR", "CLN8", "Northern epilepsy", "CLN8 disease, EPMR (subtype)", "NCL, Northern epilepsy variant", "neuronal ceroid lipofuscinosis 8", "ceroid lipofuscinosis neuronal 8", "CLN8 disease, late infantile (subtype)", "CLN8 disease, Northern epilepsy variant", "epilepsy mental deterioration Finnish type", "epilepsy, progressive, with mental retardation", "epilepsy, progressive, with intellectual disability", "neuronal ceroid lipofuscinosis, Northern epilepsy variant", "neuronal ceroid lipofuscinosis 8 northern epilepsy variant", "progressive epilepsy - intellectual disability, Finnish type", "ceroid lipofuscinosis, neuronal, 8, NORTHERN epilepsy variant", "progressive epilepsy with mental retardation, northern epilepsy", "progressive epilepsy-intellectual disability syndrome, Finnish type", "progressive epilepsy with intellectual disability, northern epilepsy", "northern epilepsy variant, neuronal ceroid lipofuscinosis, Northern epilepsy variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuronal ceroid lipofuscinosis 8 northern epilepsy variant", "shortest_name_length": 4}
{"curie": "UMLS:C0149821", "names": ["ACUTE ALCOHOL WITHDRAWAL", "ALCOHOL WITHDRAWAL ACUTE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ACUTE ALCOHOL WITHDRAWAL", "shortest_name_length": 24}
{"curie": "UMLS:C0919939", "names": ["graft thrombosis", "Graft thrombosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Graft thrombosis", "shortest_name_length": 16}
{"curie": "UMLS:C4744526", "names": ["Supratentorial Pleomorphic Xanthoastrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Supratentorial Pleomorphic Xanthoastrocytoma", "shortest_name_length": 44}
{"curie": "MONDO:0019691", "names": ["SRP", "short rib syndrome", "Short rib syndrome", "Short rib dysplasia", "rib syndrome; short", "short rib; syndrome", "short; rib syndrome", "syndrome; short rib", "short rib dysplasia", "Short rib dysplasia (disorder)", "short rib syndrome (diagnosis)", "ciliopathies with major skeletal involvement", "Ciliopathies with major skeletal involvement", "short-rib dysplasia (with or without polydactyly)", "osteochondrodysplasia with defects of growth of tubular bones and spine short rib syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short rib dysplasia", "shortest_name_length": 3}
{"curie": "UMLS:C0334412", "names": ["steroid cell tumor", "Steroid cell tumor", "Masculinovoblastoma", "Steroid cell tumour", "cell steroid tumors", "tumor; fat cell, ovary", "Ovarian Lipid Cell Tumor", "Lipid cell tumor of ovary", "Lipid Cell Tumor of Ovary", "Lipoid cell tumor of ovary", "Ovarian Steroid Cell Tumor", "lipoid cell tumor of ovary", "Lipid cell tumour of ovary", "Lipoid cell tumour of ovary", "Steroid Cell Tumor of Ovary", "Ovarian Lipid Cell Neoplasm", "Lipid Cell Neoplasm of Ovary", "Ovarian Lipoid Cell Neoplasm", "Ovarian Steroid Cell Neoplasm", "Lipid Cell Tumor of the Ovary", "Steroid Cell Tumor of the Ovary", "Lipid Cell Neoplasm of the Ovary", "lipoid cell tumor of ovary (diagnosis)", "Lipid cell tumor of ovary (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lipid cell tumor of ovary", "shortest_name_length": 18}
{"curie": "UMLS:C1334376", "names": ["Laryngeal Precancerous Condition", "Laryngeal Premalignant Condition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laryngeal Precancerous Condition", "shortest_name_length": 32}
{"curie": "UMLS:C4553253", "names": ["IIA", "Stage IIA Prostate Cancer", "Stage IIA Prostate Cancer AJCC v8", "Stage IIA Prostate Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Prostate Cancer AJCC v8", "shortest_name_length": 3}
{"curie": "MONDO:0045056", "names": ["Grade 2 Meningioma", "grade 2 meningioma", "Grade II Meningioma", "grade II meningioma", "WHO Grade 2 Meningioma", "WHO Grade II Meningioma", "WHO grade II meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "grade II meningioma", "shortest_name_length": 18}
{"curie": "UMLS:C2987393", "names": ["Poorly Cohesive Gastric Carcinoma", "Gastric Poorly Cohesive Carcinoma", "Poorly Cohesive Gastric Adenocarcinoma", "Gastric Poorly Cohesive Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Poorly Cohesive Adenocarcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C4553879", "names": ["Stage IVB Thyroid Gland Follicular Cancer", "Stage IVB Thyroid Gland Follicular Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Thyroid Gland Follicular Carcinoma AJCC v8", "shortest_name_length": 41}
{"curie": "UMLS:C0740304", "names": ["COPD exacerbation", "COPD EXACERBATION", "exacerbation copd", "copd exacerbation", "Chronic obstructive airways disease exacerbated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "COPD exacerbation", "shortest_name_length": 17}
{"curie": "MONDO:0011232", "names": ["Mhp2", "FHM2", "MHP2", "MIGRAINE, FAMILIAL BASILAR", "migraine, familial basilar", "Migraine, Familial Basilar", "familial hemiplegic migraine 2", "Familial hemiplegic migraine-2", "migraine, familial hemiplegic, 2", "MIGRAINE, FAMILIAL HEMIPLEGIC, 2", "Migraine, familial hemiplegic, 2", "familial hemiplegic migraine type 2", "hemiplegic migraine, familial type 2", "Familial hemiplegic migraine, type 2", "Hemiplegic migraine, familial type 2", "migraine, familial hemiplegic, type 2", "ATP1A2 familial or sporadic hemiplegic migraine", "familial or sporadic hemiplegic migraine caused by mutation in ATP1A2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "migraine, familial hemiplegic, 2", "shortest_name_length": 4}
{"curie": "MONDO:0017003", "names": ["partial monosomy of chromosome X", "partial deletion of chromosome X", "partial deletion of chromosome type X"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of chromosome X", "shortest_name_length": 32}
{"curie": "MONDO:0002196", "names": ["perinatal intestinal perforation", "Perinatal intestinal perforation", "bowel; perforation, fetus or newborn", "perforation; bowel, fetus or newborn", "Perinatal intestinal perforation (disorder)", "perinatal intestinal perforation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "perinatal intestinal perforation", "shortest_name_length": 32}
{"curie": "UMLS:C4763498", "names": ["Welding Exposure", "Welding dust and fumes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Welding Exposure", "shortest_name_length": 16}
{"curie": "MONDO:0005188", "names": ["iatrogenic Kaposi sarcoma", "Iatrogenic Kaposi Sarcoma", "Iatrogenic Kaposi's Sarcoma", "iatrogenic Kaposi's sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "iatrogenic Kaposi's sarcoma", "shortest_name_length": 25}
{"curie": "UMLS:C4330706", "names": ["Monogenic Hyperinsulinism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Monogenic Hyperinsulinism", "shortest_name_length": 25}
{"curie": "MONDO:0012891", "names": ["PCH2C", "Pontocerebellar Hypoplasia Type 2C", "pontocerebellar hypoplasia type 2C", "pontocerebellar hypoplasia, type 2C", "PONTOCEREBELLAR HYPOPLASIA, TYPE 2C", "TSEN34 non-syndromic pontocerebellar hypoplasia", "non-syndromic pontocerebellar hypoplasia caused by mutation in TSEN34"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pontocerebellar hypoplasia type 2C", "shortest_name_length": 5}
{"curie": "MONDO:0017362", "names": ["neuralgic amyotrophy", "brachial plexus neuritis", "neuralgic shoulder amyotrophy", "acute brachial plexus neuritis", "immune brachial plexus neuropathy", "mononeuritis multiplex with brachial predilection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuralgic amyotrophy", "shortest_name_length": 20}
{"curie": "UMLS:C0474800", "names": ["Benign squamous cell tumor", "Benign Squamous Cell Tumor", "Benign squamous cell tumour", "Benign Epidermoid Cell Tumor", "Benign Squamous Cell Neoplasm", "Benign Epidermoid Cell Neoplasm", "Benign squamous cell tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign squamous cell tumor", "shortest_name_length": 26}
{"curie": "UMLS:C4330845", "names": ["Nutritional Rickets"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nutritional Rickets", "shortest_name_length": 19}
{"curie": "MONDO:0011626", "names": ["Aoch", "AOCH", "acromegaloid features, overgrowth, cleft palate and hernia", "ACROMEGALOID FEATURES, OVERGROWTH, CLEFT PALATE, AND HERNIA", "Acromegaloid features, overgrowth, cleft palate, and hernia", "acromegaloid features, overgrowth, cleft palate, and hernia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acromegaloid features, overgrowth, cleft palate, and hernia", "shortest_name_length": 4}
{"curie": "MONDO:0006350", "names": ["Papillary urothelial carcinoma", "Papillary Transitional Carcinoma", "papillary transitional carcinoma", "Papillary transitional cell carcinoma", "Papillary Transitional Cell Carcinoma", "papillary transitional cell carcinoma", "papillary transitional cell carcinoma (diagnosis)", "Papillary transitional cell carcinoma (morphologic abnormality)", "papillary transitional cell carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papillary transitional cell carcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0010426", "names": ["XECD", "X-linked endothelial corneal dystrophy", "ENDOTHELIAL CORNEAL DYSTROPHY, X-LINKED", "endothelial corneal dystrophy, X-linked", "Endothelial Corneal Dystrophy, X-Linked", "X-linked endothelial dystrophy of cornea", "Corneal Dystrophy, Endothelial, X-Linked", "CORNEAL DYSTROPHY, ENDOTHELIAL, X-LINKED", "corneal dystrophy, endothelial, X-linked", "X-linked endothelial dystrophy of cornea (disorder)", "corneal dystrophy, endothelial, X-linked, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked endothelial corneal dystrophy", "shortest_name_length": 4}
{"curie": "MONDO:0100330", "names": ["latent infection", "disease arising from reactivation of latent virus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disease arising from reactivation of latent virus", "shortest_name_length": 16}
{"curie": "UMLS:C4524796", "names": ["Gastric Cancer by AJCC v8 Stage", "Gastric Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Cancer by AJCC v8 Stage", "shortest_name_length": 31}
{"curie": "UMLS:C1334315", "names": ["Kadish Stage A Olfactory Neuroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kadish Stage A Olfactory Neuroblastoma", "shortest_name_length": 38}
{"curie": "MONDO:0014747", "names": ["RDICC", "retinal dystrophy and iris coloboma with or without cataract", "RETINAL DYSTROPHY AND IRIS COLOBOMA WITH OR WITHOUT CONGENITAL CATARACT", "retinal dystrophy and iris coloboma with or without congenital cataract", "familial progressive retinal dystrophy-iris coloboma-congenital cataract syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial progressive retinal dystrophy-iris coloboma-congenital cataract syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0011844", "names": ["DYT15", "myoclonic dystonia 15", "Dystonia 15, myoclonic", "dystonia 15, myoclonic", "dystonia-15, myoclonic", "DYSTONIA 15, MYOCLONIC", "myoclonic dystonia type 15"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myoclonic dystonia 15", "shortest_name_length": 5}
{"curie": "UMLS:C0345562", "names": ["Benign Uvula Tumor", "Benign Uvular Tumor", "Benign Uvula Tumour", "benign tumor of uvula", "Benign Uvula Neoplasm", "Benign tumor of uvula", "Benign Uvular Neoplasm", "Benign tumour of uvula", "benign neoplasm of uvula", "Benign neoplasm of uvula", "Benign neoplasm of the uvula", "Benign neoplasm of uvula (disorder)", "benign neoplasm of uvula (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign neoplasm of uvula", "shortest_name_length": 18}
{"curie": "UMLS:C1868844", "names": ["Injection site laceration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site laceration", "shortest_name_length": 25}
{"curie": "MONDO:0021311", "names": ["parathyroid cancer", "cancer parathyroids", "of parathyroid cancer", "parathyroid gland cancer", "malignant parathyroid tumor", "cancer of parathyroid gland", "Parathyroid tumor malignant", "Malignant Parathyroid Tumor", "Parathyroid tumour malignant", "malignant tumor of parathyroid", "Malignant Tumor of Parathyroid", "malignant parathyroid neoplasm", "Malignant Parathyroid Neoplasm", "Malignant Parathyroid Gland Tumor", "malignant parathyroid gland tumor", "Malignant Neoplasm of Parathyroid", "malignant neoplasm of parathyroid", "malignant tumor of the parathyroid", "Malignant Tumor of the Parathyroid", "Malignant Parathyroid Gland Neoplasm", "Malignant Tumor of Parathyroid Gland", "malignant parathyroid gland neoplasm", "Malignant tumor of parathyroid gland", "malignant tumor of parathyroid gland", "Malignant Neoplasm of the Parathyroid", "malignant neoplasm of the parathyroid", "Malignant tumour of parathyroid gland", "Malignant neoplasm of parathyroid gland", "malignant neoplasm of parathyroid gland", "Malignant Neoplasm of Parathyroid Gland", "Malignant Tumor of the Parathyroid Gland", "malignant tumor of the parathyroid gland", "Malignant Neoplasm of the Parathyroid Gland", "malignant neoplasm of the parathyroid gland", "Malignant tumor of parathyroid gland (disorder)", "malignant neoplasm of parathyroid gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant tumor of parathyroid gland", "shortest_name_length": 18}
{"curie": "MONDO:0015273", "names": ["CAVC", "AVSD; complete", "Persistent A-V Canal", "Atrioventricular canal", "Complete common AV canal", "complete AV septal defect", "Atrioventricular canal, NOS", "Common atrioventricular valve", "COMMON ATRIOVENTRICULAR CANAL", "Common atrioventricular canal", "ATRIOVENTRICULAR CANAL, COMMON", "canal; atrioventricular common", "common; atrioventricular canal", "Complete atrioventricular canal", "atrioventricular; canal, common", "complete atrioventricular canal", "Ostium atrioventriculare commune", "ostium atrioventriculare commune", "Persistent Atrioventricular Canal", "PERSISTENT ATRIOVENTRICULAR CANAL", "Persistent atrioventricular canal", "atrioventriculare; ostium commune", "atrioventricular; canal persistent", "persistent; atrioventricular canal", "common atrioventricular canal inlet", "Complete atrioventricular canal defect", "Complete atrioventricular septal defect", "complete atrioventricular septal defect", "Common atrioventricular canal (disorder)", "Endocardial cushion defect, complete type", "complete atrioventricular canal (diagnosis)", "Endocardial cushion ventricular septal defect", "common atrioventricular canal inlet (diagnosis)", "complete atrioventricular septal defect (diagnosis)", "Atrioventricular canal type ventricular septal defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complete atrioventricular canal", "shortest_name_length": 4}
{"curie": "MONDO:0014953", "names": ["IDDCA", "intellectual developmental disorder with cardiac arrhythmia", "Intellectual Developmental Disorder with Cardiac Arrhythmia", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC ARRHYTHMIA", "gnb5-related intellectual disability-cardiac arrhythmia syndrome", "GNB5-related intellectual disability-cardiac arrhythmia syndrome", "GNB5-related intellectual disability, cardiac arrhythmia syndrome", "intellectual developmental disorder with cardiac arrhythmia; IDDCA", "G protein subunit beta 5-related intellectual disability, cardiac arrhythmia syndrome", "G protein subunit beta 5-related intellectual disability, cardiac arrhythmia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gnb5-related intellectual disability-cardiac arrhythmia syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0008393", "names": ["RSTS", "RSTS1", "Rubinstein syndrome", "Rubinstein-Taybi syndrome 1", "broad thumb-hallux syndrome", "RUBINSTEIN-TAYBI SYNDROME 1", "CREBBP Rubinstein-Taybi syndrome", "Rubinstein-Taybi Syndrome Type 1", "Rubinstein-Taybi syndrome type 1", "Rubinstein-Taybi syndrome due to CREBBP mutations", "Rubinstein-Taybi syndrome caused by mutation in CREBBP", "broad thumbs and great toes, characteristic facies, and mental retardation", "broad thumbs and great toes, characteristic facies, and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rubinstein-Taybi syndrome due to CREBBP mutations", "shortest_name_length": 4}
{"curie": "UMLS:C2699776", "names": ["DLBCL-CI", "Diffuse Large B-Cell Lymphoma Associated with Chronic Inflammation", "Diffuse large B-cell lymphoma associated with chronic inflammation", "DLBCL (diffuse large B-cell lymphoma) associated with chronic inflammation", "Diffuse large B-cell lymphoma associated with chronic inflammation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse large B-cell lymphoma associated with chronic inflammation", "shortest_name_length": 8}
{"curie": "MONDO:0006052", "names": ["lung TB", "Lung TB", "phthisis", "PHTHISIS", "Phthisis", "pulmonary TB", "Pulmonary TB", "Lung Tuberculosis", "lung tuberculosis", "Pulmonary Phthisis", "Pulmonary Phthises", "Phthisis, Pulmonary", "Phthises, Pulmonary", "Tuberculosis of lung", "Pulmonary Consumption", "Pulmonary Tuberculoses", "Pulmonary tuberculosis", "Pulmonary Tuberculosis", "pulmonary tuberculoses", "pulmonary; tuberculous", "PULMONARY TUBERCULOSIS", "Consumption, Pulmonary", "pulmonary tuberculosis", "Pulmonary Consumptions", "Tuberculoses, Pulmonary", "Consumptions, Pulmonary", "Tuberculosis, pulmonary", "tuberculosis; pulmonary", "TUBERCULOSIS, PULMONARY", "Tuberculosis, Pulmonary", "respiratory tuberculosis", "Respiratory tuberculosis", "tuberculosis respiratory", "Tuberculosis;respiratory", "Tuberculosis respiratory", "Tuberculosis of lung NOS", "tuberculosis; respiratory", "TB - Pulmonary tuberculosis", "lung; infection, tuberculous", "infection; lung, tuberculous", "Respiratory tuberculosis NOS", "PTB - Pulmonary tuberculosis", "RTB - Respiratory tuberculosis", "Pulmonary tuberculosis (disorder)", "Tuberculosis of respiratory system", "Unspecified pulmonary tuberculosis", "pulmonary tuberculosis (diagnosis)", "Pulmonary tuberculosis, unspecified", "tuberculosis respiratory (diagnosis)", "Drug-sensitive pulmonary tuberculosis", "Tuberculosis respiratory (excluding A70)", "Tuberculosis of respiratory system (disorder)", "Pulmonary tuberculosis, unspecified, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary tuberculosis", "shortest_name_length": 7}
{"curie": "UMLS:C0568062", "names": ["METHOTREXATE TOXICITY", "methotrexate toxicity", "Methotrexate toxicity", "Methotrexate Toxicity", "Methotrexate poisoning", "Poisoning by methotrexate", "toxicity from methotrexate", "methotrexate toxicity (diagnosis)", "Methotrexate poisoning (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Methotrexate poisoning", "shortest_name_length": 21}
{"curie": "MONDO:0001795", "names": ["Plantar wart", "PLANTAR WART", "plantar wart", "Plantar Wart", "wart plantar", "plantars wart", "plantar warts", "Plantar Warts", "PLANTAR WARTS", "Plantar warts", "warts plantar", "Verruca pedis", "verruca pedis", "plantar's wart", "plantars warts", "plantar's warts", "Wart(s);plantar", "verruca plantaris", "Verruca plantaris", "Verruca Plantaris", "VP - verruca pedis", "VP - Verrucae pedis", "plantar warts (diagnosis)", "Verruca plantaris (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "plantar wart", "shortest_name_length": 12}
{"curie": "MONDO:0002380", "names": ["Myoepithelioma", "myoepithelioma", "Myoepitheliomas", "Myoepithelial Tumor", "myoepithelial tumor", "Myoepithelial tumor", "Myoepithelial tumour", "Tumor, Myoepithelial", "Myoepithelial Tumors", "myoepithelial adenoma", "Myoepithelial adenoma", "Benign myoepithelioma", "Benign Myoepithelioma", "benign myoepithelioma", "Tumors, Myoepithelial", "MYOEPITHELIOMA, BENIGN", "Myoepithelial Neoplasm", "myoepithelial neoplasm", "Myoepithelial neoplasm", "Myoepithelial Tumor of Soft Tissue", "Myoepithelioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myoepithelial tumor", "shortest_name_length": 14}
{"curie": "MONDO:0018551", "names": ["patent urachus", "urachus patent", "Patent Urachus", "Patent urachus", "Patent of urachus", "Persistent urachus", "Patent urachal duct", "persistent; urachus", "urachus; persistent", "patent urachus (disease)", "Patent urachus (disorder)", "Persistent umbilical sinus", "patent urachus (diagnosis)", "urachus; patent or persistent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "patent urachus", "shortest_name_length": 14}
{"curie": "UMLS:C4684888", "names": ["Refractory Alveolar Rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Alveolar Rhabdomyosarcoma", "shortest_name_length": 36}
{"curie": "UMLS:C0085742", "names": ["Acute Brain Injury", "Injury, Acute Brain", "Brain Injury, Acute", "Acute Brain Injuries", "Injuries, Acute Brain", "Brain Injuries, Acute"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injuries, Acute Brain", "shortest_name_length": 18}
{"curie": "UMLS:C0751633", "names": ["carotid artery plaque", "Carotid Artery Plaque", "Artery Plaque, Carotid", "Carotid Artery Plaques", "Plaque, Carotid Artery", "Artery Plaques, Carotid", "Plaques, Carotid Artery", "carotid artery plaque (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carotid Artery Plaque", "shortest_name_length": 21}
{"curie": "MONDO:0012626", "names": ["MKS4", "Meckel syndrome 4", "Meckel syndrome type 4", "CEP290 Meckel syndrome", "Meckel syndrome, type 4", "MECKEL SYNDROME, TYPE 4", "Meckel Syndrome, Type 4", "Meckel-Gruber syndrome, type 4", "MECKEL-GRUBER SYNDROME, TYPE 4", "Meckel-Gruber Syndrome, Type 4", "Meckel syndrome type 4 (diagnosis)", "Meckel-Like Cerebrorenodigital Syndrome", "MECKEL-LIKE CEREBRORENODIGITAL SYNDROME", "Meckel-like Cerebrorenodigital syndrome", "Meckel syndrome caused by mutation in CEP290"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meckel syndrome, type 4", "shortest_name_length": 4}
{"curie": "MONDO:0017255", "names": ["Panuveitis", "panuveitis", "total uveitis", "Total uveitis", "Diffuse uveitis", "diffuse uveitis", "panuveitis (disease)", "Panuveitis (disorder)", "panuveitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "panuveitis", "shortest_name_length": 10}
{"curie": "MONDO:0100020", "names": ["pseudo-Lennox syndrome", "atypical benign partial epilepsy of childhood", "atypical childhood epilepsy with centrotemporal spikes", "atonic-benign childhood epilepsy with centrotemporal spikes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical childhood epilepsy with centrotemporal spikes", "shortest_name_length": 22}
{"curie": "MONDO:0014469", "names": ["DFNB103", "autosomal recessive deafness 103", "deafness, autosomal recessive 103", "DEAFNESS, AUTOSOMAL RECESSIVE 103", "deafness, autosomal recessive type 103", "autosomal recessive nonsyndromic deafness 103", "CLIC5 autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 103", "autosomal recessive nonsyndromic deafness type 103", "autosomal recessive nonsyndromic deafness caused by mutation in CLIC5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 103", "shortest_name_length": 7}
{"curie": "MONDO:0013972", "names": ["PRLTS2", "Perrault syndrome 2", "PERRAULT SYNDROME 2", "HARS2 Perrault syndrome", "Perrault syndrome type 2", "Perrault syndrome caused by mutation in HARS2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perrault syndrome 2", "shortest_name_length": 6}
{"curie": "UMLS:C2936351", "names": ["Fibroatheroma", "Fibroatheromas", "Fibroatheromatous Plaque", "Fibroatheromatous Plaques", "Plaque, Fibroatheromatous"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fibroatheroma", "shortest_name_length": 13}
{"curie": "UMLS:C1710409", "names": ["ADENOMA, LIGHT CELL, BENIGN", "Thyroid Gland Clear Cell Follicular Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Clear Cell Follicular Adenoma", "shortest_name_length": 27}
{"curie": "MONDO:0006279", "names": ["Lung Sarcomatoid Carcinoma", "lung sarcomatoid carcinoma", "Sarcomatoid carcinoma of lung", "pulmonary sarcomatoid carcinoma", "sarcomatoid carcinoma of the lung", "Sarcomatoid carcinoma of the lung", "pseudosarcomatous carcinoma of lung", "Pseudosarcomatous carcinoma of lung", "Primary pseudosarcomatous carcinoma of lung", "Pseudosarcomatous carcinoma of lung (disorder)", "pseudosarcomatous carcinoma of lung (diagnosis)", "Primary pseudosarcomatous carcinoma of lung (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung sarcomatoid carcinoma", "shortest_name_length": 26}
{"curie": "UMLS:C1168220", "names": ["Stage III Extrahepatic Bile Duct Cancer", "stage III extrahepatic bile duct cancer", "Extrahepatic Bile Duct Cancer Stage III", "Extrahepatic bile duct cancer stage III", "Stage III Extrahepatic Bile Duct Carcinoma", "Stage III Carcinoma of Extrahepatic Bile Duct", "Stage III Carcinoma of the Extrahepatic Bile Duct"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extrahepatic bile duct cancer stage III", "shortest_name_length": 39}
{"curie": "MONDO:0019371", "names": ["Narcolepsy type 2", "Narcolepsy without cataplexy", "narcolepsy without cataplexy", "Narcolepsy, without cataplexy", "Narcolepsy without cataplexy (disorder)", "narcolepsy without cataplexy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "narcolepsy without cataplexy", "shortest_name_length": 17}
{"curie": "UMLS:C4329968", "names": ["Factor VII Inactivation", "Factor VII Inhibitor Present"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Factor VII Inactivation", "shortest_name_length": 23}
{"curie": "UMLS:C1334740", "names": ["Metastatic SRC Breast Carcinoma", "Metastatic SRC Carcinoma of Breast", "Metastatic SRC Carcinoma of the Breast", "Metastatic Signet Ring Cell Breast Carcinoma", "Metastatic Breast Signet-Ring Cell Carcinoma", "Metastatic Breast Signet Ring Cell Carcinoma", "Metastatic Mammary Signet Ring Cell Carcinoma", "Metastatic Signet Ring Cell Carcinoma of Breast", "Metastatic Signet Ring Cell Carcinoma of the Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Breast Signet Ring Cell Carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0021571", "names": ["MS", "MS1", "DISSEMINATED SCLEROSIS", "disseminated sclerosis", "susceptibility to multiple sclerosis", "multiple sclerosis, susceptibility to", "MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO", "multiple sclerosis, susceptibility to 1", "MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO, 1", "multiple sclerosis, susceptibility to, 1", "multiple sclerosis, disease progression, modifier of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple sclerosis, susceptibility to 1", "shortest_name_length": 2}
{"curie": "UMLS:C1449720", "names": ["Pubertal gynecomastia", "pubertal gynecomastia", "Pubertal Gynecomastia", "Transient Gynecomastia", "Pubertal gynaecomastia", "Adolescent Gynecomastia", "Gynecomastia, Adolescent", "Pubertal gynecomastia (disorder)", "pubertal gynecomastia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adolescent Gynecomastia", "shortest_name_length": 21}
{"curie": "MONDO:0014833", "names": ["HBMS", "NEDHBM", "heart and brain malformation syndrome", "HEART AND BRAIN MALFORMATION SYNDROME", "heart and brain malformation syndrome; HBMS", "NEURODEVELOPMENTAL DISORDER WITH HEART AND BRAIN MALFORMATIONS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heart and brain malformation syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0005995", "names": ["trichostrongylosis", "Trichostrongylosis", "Trichostrongyloses", "TRICHOSTRONGYLIASIS", "Trichostrongyliasis", "trichostrongyliasis", "Trichostrongylus; infection", "Infection by Trichostrongylus", "infection by Trichostrongylus", "Trichostrongylus; infestation", "infestation; Trichostrongylus", "Trichostrongyliasis (disorder)", "trichostrongyliasis (diagnosis)", "Trichostrongylus infectious disease", "Trichostrongylus disease or disorder", "infection by Trichostrongylus species", "Infection by Trichostrongylus species", "Trichostrongylus caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichostrongylosis", "shortest_name_length": 18}
{"curie": "MONDO:0017703", "names": ["disorder of glyoxylate metabolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of glyoxylate metabolism", "shortest_name_length": 33}
{"curie": "UMLS:C0278824", "names": ["Stage III Bladder Cancer", "Bladder cancer stage III", "stage III bladder cancer", "bladder cancer, stage III", "Carcinoma bladder stage III", "Stage III Bladder Carcinoma", "Bladder carcinoma stage III", "Cancer of Bladder Stage III", "Stage III Carcinoma of Bladder", "Cancer of the Bladder Stage III", "stage III cancer of the bladder", "Stage III Bladder Cancer AJCC v6", "Stage III Bladder Cancer AJCC v7", "cancer of the bladder, stage III", "stage III carcinoma of the bladder", "Stage III Carcinoma of the Bladder", "carcinoma of the bladder, stage III", "Carcinoma urinary bladder stage III", "Stage III Bladder Carcinoma AJCC v6", "Stage III Urinary Bladder Carcinoma", "Stage III Bladder Carcinoma AJCC v7", "Urinary bladder carcinoma stage III", "Jewett-Marshall Stage C Bladder Cancer", "Stage III Carcinoma of Urinary Bladder", "Stage III Bladder Cancer AJCC v6 and v7", "Stage III Carcinoma of the Urinary Bladder", "Jewett-Marshall Stage C Urinary Bladder Cancer", "Jewett-Marshall Stage C Urinary Bladder Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Bladder Cancer AJCC v6 and v7", "shortest_name_length": 24}
{"curie": "UMLS:C0679247", "names": ["terminal disease", "terminal illness", "disease terminal", "Terminal illness", "Terminal Illness", "Terminal disease", "illness terminal", "Terminal Disease", "diseases terminal", "end stage disease", "disease end stage", "illnesses terminal", "Terminal illness (finding)", "terminal illness (physical finding)", "general body state finding illness terminal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Terminal illness", "shortest_name_length": 16}
{"curie": "MONDO:0005968", "names": ["Schenck", "De Beurmann", "Beurmann, De", "sporotrichosis", "SPOROTRICHOSIS", "Sporotrichosis", "Sporotrichoses", "schenck disease", "SCHENCK DISEASE", "BEURMANN DISEASE", "Sporotrichosis NOS", "Sporothrix Infection", "Sporothrix Infections", "Infection, Sporothrix", "rose gardener's disease", "Sporotrichosis (disorder)", "sporotrichosis (diagnosis)", "Sporotrichosis, unspecified", "Infection by Sporothrix schenkii"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sporotrichosis", "shortest_name_length": 7}
{"curie": "MONDO:0005053", "names": ["ischemia", "Ischemia", "ISCHEMIA", "Ischemias", "ischaemia", "Ischaemia", "Ischemia NOS", "Ischemia, NOS", "Ischaemia NOS", "Ischaemia, NOS", "ischemic disease", "Ischemia (disorder)", "ischemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ischemic disease", "shortest_name_length": 8}
{"curie": "MONDO:0002701", "names": ["Mucinous cystadenocarcinoma ovary", "ovary mucinous cystadenocarcinoma", "ovarian mucinous cystadenocarcinoma", "cystadenocarcinoma mucinous ovaries", "Ovarian Mucinous Cystadenocarcinoma", "mucinous cystadenocarcinoma of ovary", "cystadenocarcinoma, ovarian mucinous", "Mucinous cystadenocarcinoma of ovary", "Mucinous Cystadenocarcinoma of Ovary", "cystadenocarcinoma, mucinous, ovarian", "Mucinous Cystadenocarcinoma of the Ovary", "mucinous cystadenocarcinoma of the ovary", "cystadenocarcinoma of the ovary, mucinous", "ovary cancer, mucinous cystadenocarcinoma", "OVARIAN CANCER MUCINOUS CYSTADENOCARCINOMA", "ovarian cancer, mucinous cystadenocarcinoma", "Mucinous cystadenocarcinoma of ovary (disorder)", "mucinous cystadenocarcinoma of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian mucinous cystadenocarcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0018961", "names": ["MLM", "DNS", "FAMMM", "FAMM Syndrome", "FAMMM syndrome", "FAMM-PC syndrome", "Familial Melanoma", "Familial melanoma", "B-K mole syndrome", "familial melanoma", "MELANOMA, FAMILIAL", "Melanoma, Familial", "Hereditary Melanoma", "Familial Cutaneous Melanoma", "hereditary multiple melanoma", "Hereditary Cutaneous Melanoma", "hereditary melanoma (disease)", "melanoma, hereditary, multiple", "Familial atypical mole syndrome", "Familial dysplastic nevus syndrome", "Melanoma-pancreatic cancer syndrome", "Hereditary Cutaneous (Skin) Melanoma", "DYSPLASTIC NEVUS SYNDROME, HEREDITARY", "Familial Atypical Mole Melanoma Syndrome", "Familial atypical multiple mole melanoma syndrome", "FAMILIAL ATYPICAL MOLE-MALIGNANT MELANOMA SYNDROME", "Familial atypical multiple mole melanoma-pancreatic carcinoma syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial melanoma", "shortest_name_length": 3}
{"curie": "UMLS:C0855007", "names": ["PNET of bone localised", "Localized PNET of Bone", "PNET of bone localized", "Localized Neuroepithelioma of Bone", "Peripheral neuroepithelioma of bone localized", "Peripheral neuroepithelioma of bone localised", "Localized Peripheral Primitive Neuroectodermal Tumor of Bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PNET of bone localised", "shortest_name_length": 22}
{"curie": "MONDO:0010435", "names": ["NYS6", "congenital nystagmus 6", "X-linked congenital nystagmus 6", "NYSTAGMUS 6, congenital, X-linked", "nystagmus 6, congenital, X-linked", "NYSTAGMUS 6, CONGENITAL, X-LINKED", "NYSTAGMUS, 6, CONGENITAL, X-LINKED", "nystagmus 6, congenital, X-linked, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nystagmus 6, congenital, X-linked", "shortest_name_length": 4}
{"curie": "UMLS:C4521746", "names": ["IIIA", "Stage IIIA Esophageal Squamous Cell Cancer", "Pathologic Stage IIIA Esophageal Squamous Cell Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IIIA Esophageal Squamous Cell Carcinoma AJCC v8", "shortest_name_length": 4}
{"curie": "UMLS:C0278984", "names": ["stage IIIB NSCLC", "Stage IIIB NSCLC", "NSCLC, stage IIIB", "non-oat cell lung cancer, stage IIIB", "stage IIIB nonsmall cell lung cancer", "Non Small Cell Lung Cancer Stage IIIB", "stage IIIB non-small cell lung cancer", "Non-small cell lung cancer stage IIIB", "nonsmall cell lung cancer, stage IIIB", "Stage IIIB Non-Small Cell Lung Cancer", "Lung cancer non-small cell stage IIIB", "lung cancer, non-oat cell, stage IIIB", "Non Small Cell Lung Cancer, Stage IIIB", "Stage IIIB Non-Oat Cell Lung Carcinoma", "lung cancer, nonsmall cell, stage IIIB", "non-small cell lung cancer, stage IIIB", "lung cancer, non-small cell, stage IIIB", "Stage IIIB Non-Small Cell Lung Carcinoma", "Stage IIIB Non-Oat Cell Carcinoma of Lung", "Stage IIIB Non-Small Cell Carcinoma of Lung", "Stage IIIB Lung Non-Small Cell Cancer AJCC v7", "Stage IIIB Non-Small Cell Lung Cancer AJCC v7", "Stage IIIB Non-Oat Cell Carcinoma of the Lung", "Stage IIIB Non-Small Cell Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-small cell lung cancer stage IIIB", "shortest_name_length": 16}
{"curie": "MONDO:0006150", "names": ["Colon Burkitt Lymphoma", "colon Burkitt lymphoma", "colon Burkitts lymphoma", "colon Burkitt's lymphoma", "Colon Burkitt's Lymphoma", "Burkitt lymphoma of colon", "Burkitts lymphoma of colon", "Primary Colon Burkitt's Lymphoma", "primary colon Burkitt's lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colon Burkitt lymphoma", "shortest_name_length": 22}
{"curie": "MONDO:0012554", "names": ["COFS4", "ERCC1 COFS syndrome", "cerebrooculofacioskeletal syndrome 4", "Cerebrooculofacioskeletal Syndrome 4", "CEREBROOCULOFACIOSKELETAL SYNDROME 4", "cerebrooculofacioskeletal syndrome type 4", "COFS syndrome caused by mutation in ERCC1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebrooculofacioskeletal syndrome 4", "shortest_name_length": 5}
{"curie": "UMLS:C0279959", "names": ["Stage I Diffuse Mixed Cell Lymphoma", "Adult Diffuse Mixed Cell Lymphoma Stage I", "stage I adult diffuse mixed cell lymphoma", "Stage I Adult Diffuse Mixed Cell Lymphoma", "adult diffuse mixed cell lymphoma, stage I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Adult Diffuse Mixed Cell Lymphoma", "shortest_name_length": 35}
{"curie": "MONDO:0002941", "names": ["anal carcinoma", "Anal Margin Cancer", "anal margin cancer", "anal margin carcinoma", "Anal Margin Carcinoma", "Perianal Skin Carcinoma", "Perianal skin carcinoma", "perianal skin carcinoma", "Carcinoma of anal margin", "Carcinoma of Anal Margin", "carcinoma of anal margin", "Anal margin carcinoma NOS", "carcinoma of perianal skin", "anal carcinoma cell squamous", "anal squamous cell carcinoma", "Carcinoma of the Anal Margin", "carcinoma of the anal margin", "squamous cell carcinoma anal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anal margin carcinoma", "shortest_name_length": 14}
{"curie": "UMLS:C5557156", "names": ["Stage IB1 Cervical Cancer AJCC v9", "Stage IB1 Cervical Carcinoma AJCC v9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB1 Cervical Cancer AJCC v9", "shortest_name_length": 33}
{"curie": "MONDO:0022424", "names": ["Alpha-mannosidosis type 1", "alpha-mannosidosis type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alpha-mannosidosis type 1", "shortest_name_length": 25}
{"curie": "UMLS:C0151689", "names": ["hair discolor", "HAIR DISCOLORED", "Hair discolored", "Hair discoloured", "HAIR DISCOLORATION", "hair discoloration", "Hair discoloration", "discolorations hair", "hair discolouration", "HAIR DISCOLOURATION", "Hair discolouration", "Hair discoloration, NOS", "Hair discolouration, NOS", "hair discoloration (symptom)", "Hair discoloration (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hair discoloration", "shortest_name_length": 13}
{"curie": "MONDO:0004095", "names": ["B-cell NHL", "b-cell lymphoma", "B Cell Lymphoma", "B-Cell Neoplasm", "b cell lymphoma", "B-cell lymphoma", "lymphoma b cell", "B-cell neoplasm", "LYMPHOMA B CELL", "B cell lymphoma", "B-Cell Lymphoma", "cell b lymphoma", "lymphoma b-cell", "Lymphoma, B Cell", "lymphoma; B-cell", "lymphoma, B-cell", "b cells lymphoma", "B-cell; lymphoma", "Lymphoma, B-Cell", "B-Cell Lymphomas", "b cell lymphomas", "b-cell lymphomas", "Lymphomas, B-Cell", "b cells lymphomas", "B-cell lymphoma NOS", "B-cell lymphoma (clinical)", "B-cell lymphoma (disorder)", "B-cell lymphocytic neoplasm", "B-cell non-Hodgkin lymphoma", "B-Cell Non-Hodgkin Lymphoma", "B-cell lymphoma (diagnosis)", "non-Hodgkin's B-cell lymphoma", "b cell lymphoma non hodgkin's", "B-Cell Non Hodgkin's Lymphoma", "B-cell non-Hodgkin's lymphoma", "Non-Hodgkin's B-Cell Lymphoma", "non-Hodgkin's lymphoma B-cell", "B-Cell Non-Hodgkin's Lymphoma", "B-Cell non Hodgkin's lymphoma", "Non-Hodgkin's Lymphoma B-Cell", "lymphomas non-hodgkin's b-cell", "Lymphomas non-Hodgkin's B-cell", "lymphomas non-Hodgkin's B-cell", "Lymphomas Non-Hodgkin's B-Cell", "Malignant lymphoma, B-cell type", "Lymphoma, non-Hodgkin lymphoma, B-cell", "B-cell neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-cell neoplasm", "shortest_name_length": 10}
{"curie": "MONDO:0007790", "names": ["DSN", "DSS", "CMT3", "HMSN3", "CMT4f", "HMSN 3", "hmsn iii", "HMSN III", "HSMN III", "HMSN Type III", "HMSN Type IIIs", "Déjerine-Sottas", "Dejerine-Sottas Disease", "dejerine-sottas disease", "Dejerine-Sottas disease", "Dejerine Sottas Disease", "Déjérine-Sottas disease", "Dejerine Sottas disease", "dejerine sottas disease", "DEJERINE-SOTTAS DISEASE", "Dejerine-Sottas syndrome", "Disease, Dejerine-Sottas", "Dejerine Sottas Syndrome", "DEJERINE-SOTTAS SYNDROME", "Dejerine-Sottas Syndrome", "Syndrome, Dejerine-Sottas", "DéJérine-Sottas disease", "dejerines diseases sottas", "Dejerine-Sottas Neuropathy", "Dejerine-Sottas neuropathy", "DEJERINE-SOTTAS NEUROPATHY", "Dejerine Sottas Neuropathy", "Neuropathy, Dejerine-Sottas", "neuropathy; Déjerine-Sottas", "Déjerine-Sottas; neuropathic", "Hypertrophic hereditary neuropathy", "Hereditary hypertrophic neuropathy", "hypertrophic neuropathy of infancy", "Charcot-Marie-Tooth disease type 3", "Déjérine-Sottas disease (disorder)", "Charcot Marie Tooth Disease, Type 3", "CHARCOT-MARIE-TOOTH DISEASE, TYPE 3", "Charcot-Marie-Tooth Disease, Type 3", "Charcot-Marie-Tooth disease, type 3", "Neuropathy of infancy, Dejerine-Sottas", "progressive hypertrophic polyneuropathy", "Dejerine-Sottas Hypertrophic Neuropathy", "Hereditary Motor and Sensory Neuropathy 3", "neuropathy; hypertrophic, Déjerine-Sottas", "hereditary motor and sensory neuropathy 3", "hypertrophic; neuropathic, Déjerine-Sottas", "Hypertrophic Neuropathy of Dejerine-Sottas", "Hypertrophic Neuropathy of Dejerine Sottas", "hypertrophic neuropathy of Dejerine-Sottas", "HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS", "Hereditary sensory-motor neuropathy, type 3", "Hereditary sensory-motor neuropathy, type III", "Hereditary motor and sensory neuropathy type 3", "hereditary motor and sensory neuropathy type 3", "Hypertrophic demyelinative neuropathy of infancy", "Progressive hypertrophic interstitial neuropathy", "hereditary motor and sensory neuropathy type III", "Hereditary Motor and Sensory Neuropathy Type III", "Hereditary motor and sensory neuropathy type III", "HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPE III", "Hereditary motor and sensory neuropathy, type III", "neuropathy; hypertrophic, interstitial progressive", "Hereditary, Type III, Motor and Sensory Neuropathy", "progressive hypertrophic polyneuropathy (diagnosis)", "Charcot-Marie-Tooth Disease, Demyelinating, Type 4f", "progressive hypertrophic polyneuropathy (Dejerine-Sottas)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 3", "shortest_name_length": 3}
{"curie": "MONDO:0018274", "names": ["SPDRS", "ST3GAL5-CDG", "salt & pepper syndrome", "GM3 Synthase Deficiency", "GM3 synthase deficiency", "GM3 SYNTHASE DEFICIENCY", "salt-and-pepper syndrome", "salt and pepper syndrome", "Amish Infantile Epilepsy Syndrome", "AMISH INFANTILE EPILEPSY SYNDROME", "Amish infantile epilepsy syndrome", "Ganglioside GM3 synthase deficiency", "salt and pepper mental retardation syndrome", "SALT AND PEPPER MENTAL RETARDATION SYNDROME", "Infantile-onset symptomatic epilepsy syndrome", "epilepsy syndrome, infantile-onset symptomatic", "EPILEPSY SYNDROME, INFANTILE-ONSET SYMPTOMATIC", "Epilepsy Syndrome, Infantile-Onset Symptomatic", "Ganglioside GM3 synthase deficiency (disorder)", "Ganglioside GM3 synthase deficiency (diagnosis)", "salt and pepper developmental regression syndrome", "SALT AND PEPPER DEVELOPMENTAL REGRESSION SYNDROME", "lactosylceramide alpha-2,3-sialyltransferase activity disease", "disorder of lactosylceramide alpha-2,3-sialyltransferase activity", "infantile-onset symptomatic epilepsy syndrome - developmental stagnation - blindness", "infantile-onset symptomatic epilepsy syndrome-developmental stagnation-blindness syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "GM3 synthase deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0015353", "names": ["HMN5", "HMN5A", "HMN V", "DHMN5", "dHMN5", "DSMAV", "DSMAVA", "DHMN5A", "DHMN V", "HMN 5A", "Dhmn-V", "DHMN VA", "dHMN 5A", "distal HMN V", "Distal HMN V", "distal HMN VA", "Distal spinal muscular atrophy type 5", "distal spinal muscular atrophy type 5", "distal spinal muscular atrophy type VA", "Distal Spinal Muscular Atrophy, Type V", "Spinal Muscular Atrophy, Distal Type V", "Spinal Muscular Atrophy, Distal, Type V", "spinal muscular atrophy, distal, type 5", "SPINAL MUSCULAR ATROPHY, DISTAL, TYPE V", "spinal muscular atrophy, distal, type 5A", "SPINAL MUSCULAR ATROPHY, DISTAL, TYPE VA", "Distal hereditary motor neuropathy type V", "Distal hereditary motor neuropathy type 5", "distal hereditary motor neuropathy type V", "Distal Hereditary Motor Neuropathy, Type V", "Neuropathy, Distal Hereditary Motor, Type V", "Distal Hereditary Motor Neuronopathy, Type V", "distal hereditary motor neuronopathy type 5A", "neuropathy, distal hereditary motor, type 5A", "NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VA", "Neuronopathy, Distal Hereditary Motor, Type V", "NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE V", "neuronopathy, distal hereditary motor, type 5", "NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VA", "neuronopathy, distal hereditary motor, type 5A", "neuronopathy, distal hereditary motor, type VA", "dHMN5 - distal hereditary motor neuropathy type 5", "Distal hereditary motor neuropathy type 5 (disorder)", "Spinal Muscular Atrophy, Distal, With Upper Limb Predominance", "spinal muscular atrophy, distal, with upper limb predominance", "SPINAL MUSCULAR ATROPHY, DISTAL, WITH UPPER LIMB PREDOMINANCE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuronopathy, distal hereditary motor, type 5A", "shortest_name_length": 4}
{"curie": "UMLS:C4744987", "names": ["Metastatic Small Intestinal Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Small Intestinal Neuroendocrine Carcinoma", "shortest_name_length": 52}
{"curie": "UMLS:C5419762", "names": ["Metastatic Salivary Gland Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Salivary Gland Squamous Cell Carcinoma", "shortest_name_length": 49}
{"curie": "MONDO:0008558", "names": ["ITP", "itp", "AITP", "Frank", "Werlhof", "ITP, NOS", "WERLHOF DISEASE", "Werlhof Disease", "Disease, Werlhof", "Werlhofs Disease", "werlhof's disease", "Werlhof's disease", "Werlhof's Disease", "idiopathic purpura", "Disease, Werlhof's", "Idiopathic purpura", "Werlhof's syndrome", "idiopathic; purpura", "purpura; idiopathic", "immune thrombocytopenia", "Idiopathic purpura, NOS", "Immune Thrombocytopenia", "Immune thrombocytopenia", "Thrombocytopenia, Immune", "Immune Thrombocytopenias", "Thrombocytopenias, Immune", "Idiopathic Thrombocytopenia", "Autoimmune Thrombocytopenia", "idiopathic thrombocytopenia", "Autoimmune Thrombocytopenias", "Thrombocytopenia, Autoimmune", "ideopath thrombocytopenic pur", "Ideopath thrombocytopenic pur", "Thrombocytopenias, Autoimmune", "Idiopath Thrombocytopenic Purp", "Primary Immune Thrombocytopenia", "immune purpura thrombocytopenic", "Immune thrombocytopenic purpura", "thrombocytopenic purpura immune", "Primary immune thrombocytopenia", "IMMUNE THROMBOCYTOPENIC PURPURA", "immune thrombocytopenic purpura", "Immune Thrombocytopenic Purpura", "Immune Thrombocytopenic Purpuras", "Purpura, Immune Thrombocytopenic", "Thrombocytopenic Purpura, Immune", "primary thrombocytopenic purpura", "Thrombocytopenic Purpuras, Immune", "Purpuras, Immune Thrombocytopenic", "idiopathic thrombocytopenic purpura", "Autoimmune Thrombocytopenic Purpura", "Idiopathic Thrombocytopenic Purpura", "Autoimmune thrombocytopenic purpura", "autoimmune thrombocytopenic purpura", "idiopathic thrombocytopenia purpura", "thrombocytopenic purpura autoimmune", "IDIOPATHIC THROMBOCYTOPENIC PURPURA", "Idiopathic thrombocytopenic purpura", "Idiopathic thrombocytopenia purpura", "Idiopathic Thrombocytopenia Purpura", "thrombocytopenic purpura, autoimmune", "THROMBOCYTOPENIC PURPURA, AUTOIMMUNE", "Idiopathic Thrombocytopenic Purpuras", "Purpura, Idiopathic Thrombocytopenic", "Autoimmune Thrombocytopenic Purpuras", "Thrombocytopenic Purpura, Idiopathic", "Thrombocytopenic Purpura, Autoimmune", "Purpura, Autoimmune Thrombocytopenic", "thrombocytopenic; purpura, idiopathic", "Purpura, Thrombocytopenic, Autoimmune", "purpura; thrombocytopenic, idiopathic", "Purpura, Thrombocytopenic, Idiopathic", "PURPURA, THROMBOCYTOPENIC, IDIOPATHIC", "Thrombocytopenic Purpuras, Idiopathic", "Purpuras, Autoimmune Thrombocytopenic", "Purpuras, Idiopathic Thrombocytopenic", "ITP (immune thrombocytopenic purpura)", "Idiopathic thrombocytopenic purpura, NOS", "Idiopathic thrombocytopenic purpura (ITP)", "ITP (idiopathic thrombocytopenic purpura)", "idiopathic thrombocytopenic purpura (ITP)", "ITP - Idiopathic thrombocytopenic purpura", "immune thrombocytopenic purpura (diagnosis)", "idiopathic thrombocytopenic purpura (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune thrombocytopenic purpura", "shortest_name_length": 3}
{"curie": "MONDO:0011911", "names": ["CLSD", "Boyadjiev Jabs syndrome", "BOYADJIEV-JABS SYNDROME", "Boyadjiev-Jabs syndrome", "Boyadjiev-Jabs Syndrome", "craniolenticulosutural dysplasia", "CRANIOLENTICULOSUTURAL DYSPLASIA", "Craniolenticulosutural Dysplasia", "Craniolenticulosutural dysplasia", "cranio-lenticulo-sutural dysplasia, CLSD", "Craniolenticulosutural dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniolenticulosutural dysplasia", "shortest_name_length": 4}
{"curie": "UMLS:C1142463", "names": ["Blood stem cell transplant failure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Blood stem cell transplant failure", "shortest_name_length": 34}
{"curie": "MONDO:0008469", "names": ["WHYTE SYNDROME", "Whyte syndrome", "Whyte Petersen McAlister syndrome", "SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH HYPOTRICHOSIS", "Spondyloepimetaphyseal dysplasia with hypotrichosis", "spondyloepimetaphyseal dysplasia with hypotrichosis", "Spondyloepimetaphyseal dysplasia-hypotrichosis syndrome", "spondyloepimetaphyseal dysplasia-hypotrichosis syndrome", "Spondyloepimetaphyseal dysplasia, hypotrichosis syndrome", "Spondyloepimetaphyseal dysplasia, hypotrichosis syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepimetaphyseal dysplasia-hypotrichosis syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C5554636", "names": ["Advanced Large Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Large Cell Neuroendocrine Carcinoma", "shortest_name_length": 44}
{"curie": "UMLS:C0334601", "names": ["Undifferentiated Retinoblastoma", "undifferentiated retinoblastoma", "Retinoblastoma, undifferentiated", "undifferentiated; retinoblastoma", "retinoblastoma; undifferentiated", "Retinoblastoma - undifferentiated", "undifferentiated retinoblastoma (diagnosis)", "Retinoblastoma, undifferentiated (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retinoblastoma, undifferentiated", "shortest_name_length": 31}
{"curie": "MONDO:0030708", "names": ["Trichomonas cervicitis", "CERVICITIS TRICHOMONAS", "Trichomonas Cervicitis", "Trichomonas vaginalis cervicitis (disease)", "Trichomonas vaginalis caused cervicitis (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Trichomonas cervicitis", "shortest_name_length": 22}
{"curie": "UMLS:C1514418", "names": ["Peritoneal SBT", "Borderline Peritoneal Serous Tumor", "Peritoneal Serous Borderline Tumor", "Primary Peritoneal Serous Borderline Tumor", "Primary Borderline Peritoneal Epithelial Tumor", "Primary Peritoneal Borderline Epithelial Tumor", "Primary Borderline Peritoneal Epithelial Neoplasm", "Primary Peritoneal Borderline Epithelial Neoplasm", "Primary Peritoneal Serous Borderline Tumor/ Primary Peritoneal Atypical Proliferative Serous Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Peritoneal Serous Tumor", "shortest_name_length": 14}
{"curie": "UMLS:C0021124", "names": ["Impulse-Ridden Personality", "Impulse Ridden Personality", "Personality, Impulse-Ridden"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Impulse-Ridden Personality", "shortest_name_length": 26}
{"curie": "UMLS:C5555148", "names": ["Fibrocartilaginous Mesenchymoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fibrocartilaginous Mesenchymoma", "shortest_name_length": 31}
{"curie": "UMLS:C0457530", "names": ["Follicular ameloblastoma", "Follicular Ameloblastoma", "Follicular ameloblastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Follicular ameloblastoma", "shortest_name_length": 24}
{"curie": "MONDO:0022557", "names": ["oculo-cerebral dysplasia", "Oculo-cerebral dysplasia", "Behrens Baumann dust syndrome", "Behrens Baumann Dust syndrome", "Behrens-Baumann-Vogel syndrome", "microphthalmia-optic nerve dysplasia", "unilateral aplasia of the optic nerve with cryptophthalmus and contralateral microphthalmus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Behrens Baumann dust syndrome", "shortest_name_length": 24}
{"curie": "UMLS:C1879758", "names": ["Atypical medullary carcinoma", "Atypical Medullary Breast Carcinoma", "Breast Atypical Medullary Carcinoma", "atypical medullary carcinoma of breast", "atypical medullary carcinoma of breast (diagnosis)", "Infiltrating Ductal Breast Carcinoma with Medullary Features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypical Medullary Breast Carcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0024797", "names": ["Adult Brainstem Tumor", "adult brainstem tumor", "Adult Brain Stem Tumor", "adult brain stem tumor", "tumor of adult brainstem", "adult brainstem neoplasm", "Adult Brainstem Neoplasm", "Tumor of Adult Brainstem", "tumor of adult brain stem", "Tumor of Adult Brain Stem", "Adult Brain Stem Neoplasm", "adult brain stem neoplasm", "neoplasm of adult brainstem", "Neoplasm of Adult Brainstem", "Tumor of the Adult Brainstem", "brainstem neoplasm of adults", "tumor of the adult brainstem", "neoplasm of adult brain stem", "Neoplasm of Adult Brain Stem", "tumor of the adult brain stem", "Tumor of the Adult Brain Stem", "Neoplasm of the Adult Brainstem", "neoplasm of the adult brainstem", "neoplasm of the adult brain stem", "Neoplasm of the Adult Brain Stem"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult brain stem neoplasm", "shortest_name_length": 21}
{"curie": "MONDO:0003903", "names": ["benign vaginal mixed tumor", "Benign Vaginal Mixed Tumor", "vaginal spindle cell epithelioma", "Vaginal Spindle Cell Epithelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign vaginal mixed tumor", "shortest_name_length": 26}
{"curie": "UMLS:C1332479", "names": ["Cardiac Schwannoma", "Benign Heart Schwannoma", "Benign Cardiac Schwannoma", "Benign Heart Neurilemmoma", "CARDIAC SCHWANNOMA, BENIGN", "Benign Neurilemoma of Heart", "Benign Cardiac Neurilemmoma", "Schwannoma, Endocardial, Benign", "Benign Neurilemoma of the Heart"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiac Schwannoma", "shortest_name_length": 18}
{"curie": "UMLS:C0206143", "names": ["Loeffler endocarditis", "loeffler endocarditis", "Loeffler Endocarditis", "Loefflers Endocarditis", "loefflers endocarditis", "Endocarditis, Loeffler", "Loeffler's Endocarditis", "Loeffler's endocarditis", "Endocarditis, Loefflers", "Endocarditis, Loeffler's", "Eosinophilic endocarditis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Loeffler's Endocarditis", "shortest_name_length": 21}
{"curie": "MONDO:0008024", "names": ["HMN7A", "Dhmnvp", "HMN 7A", "DHMN7A", "DHMNVP", "Dhmn7A", "HMN VIIA", "Harper-Young myopath", "HARPER-YOUNG MYOPATHY", "Harper-Young Myopathy", "Harper-Young myopathy", "distal hereditary motor neuronopathy type 7A", "neuropathy, distal hereditary motor, type 7A", "distal hereditary motor neuropathy type VIIA", "SLC5A7 neuronopathy, distal hereditary motor", "NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIA", "neuronopathy, distal hereditary motor, type 7A", "Neuropathy, Distal Hereditary Motor, Type VIIA", "neuronopathy, distal hereditary motor, type VIIA", "NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIA", "SPINAL MUSCULAR ATROPHY, DISTAL, WITH VOCAL CORD PARALYSIS", "Spinal Muscular Atrophy, Distal, With Vocal Cord Paralysis", "spinal muscular atrophy, distal, with vocal cord paralysis", "distal spinal muscular atrophy with vocal cord paralysis type 7A", "neuronopathy, distal hereditary motor caused by mutation in SLC5A7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuronopathy, distal hereditary motor, type 7A", "shortest_name_length": 5}
{"curie": "UMLS:C1335258", "names": ["Stage 4 Hepatoblastoma", "PRETEXT Stage 4 Hepatoblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PRETEXT Stage 4 Hepatoblastoma", "shortest_name_length": 22}
{"curie": "MONDO:0009530", "names": ["Urbach", "Urbach-Wiethe", "lipoproteinosis", "Lipoproteinosis", "LIPOPROTEINOSIS", "lipid proteinosis", "Lipid proteinosis", "Lipoidproteinosis", "LIPOID PROTEINOSIS", "lipoid proteinosis", "Lipoid proteinosis", "PROTEINOSIS, LIPOID", "lipids; proteinosis", "Urbach Wiethe Disease", "Urbach-Wiethe disease", "URBACH-WIETHE DISEASE", "Urbach Wiethe disease", "Urbach-Wiethe Disease", "Urbach-Wiethe Syndrome", "URBACH-WIETHE SYNDROME", "urbach-wiethe syndrome", "Hyalinosis cutis et mucosae", "Hyalinosis Cutis et Mucosae", "hyalinosis cutis et mucosae", "Lipoidosis cutis et mucosae", "HYALINOSIS CUTIS ET MUCOSAE", "hyalinosis cutis Et mucosae", "lipoidosis cutis et mucosae", "proteinosis; lipid or lipoid", "Lipid proteinosis (disorder)", "lipoid; proteinosis (Urbach)", "proteinosis of Urbach; lipoid", "Urbach-Wiethe Lipoid Proteinosis", "Urbach Wiethe Lipoid Proteinosis", "Lipoid Proteinosis, Urbach-Wiethe", "LIPOID PROTEINOSIS OF URBACH AND WIETHE", "Lipoid Proteinosis of Urbach and Wiethe", "lipoid proteinosis of Urbach and Wiethe"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lipoid proteinosis", "shortest_name_length": 6}
{"curie": "MONDO:0016200", "names": ["qualitative or quantitative defects of glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase", "qualitative or quantitative defects of glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase type -"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase", "shortest_name_length": 104}
{"curie": "UMLS:C0679429", "names": ["platelet dysfunction", "Platelet dysfunction", "dysfunction platelets", "PLATELET FUNCTIONAL DISORDER", "disorders functional platelet", "platelet dysfunction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Platelet dysfunction", "shortest_name_length": 20}
{"curie": "MONDO:0016231", "names": ["CMC", "CMAL", "anomaly; capillary", "capillary; anomaly", "Capillary malformation", "capillary malformation", "CAPILLARY MALFORMATIONS", "Capillary Malformations", "Capillary malformations", "rare capillary malformation", "Congenital anomaly of capillary", "Capillary malformation (disorder)", "Capillary malformation (diagnosis)", "CAPILLARY MALFORMATIONS, CONGENITAL", "congenital malformation of capillary", "Capillary Malformations, Congenital, 1", "congenital anomaly of cardiovascular system capillary malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "capillary malformation", "shortest_name_length": 3}
{"curie": "MONDO:0011408", "names": ["SPG10", "spastic paraplegia 10", "hereditary spastic paraplegia 10", "KIF5A hereditary spastic paraplegia", "hereditary spastic paraplegia type 10", "autosomal dominant spastic paraplegia", "Autosomal dominant spastic paraplegia", "autosomal dominant spastic paraplegia 10", "SPASTIC PARAPLEGIA 10, AUTOSOMAL DOMINANT", "spastic paraplegia 10, autosomal dominant", "Spastic paraplegia 10, autosomal dominant", "Autosomal dominant spastic paraplegia type 10", "autosomal dominant spastic paraplegia type 10", "familial spastic paraplegia autosomal dominant type 10", "Autosomal dominant spastic paraplegia type 10 (disorder)", "Autosomal dominant spastic paraplegia type 10 (diagnosis)", "hereditary spastic paraplegia caused by mutation in KIF5A", "SPASTIC PARAPLEGIA 10 WITH OR WITHOUT PERIPHERAL NEUROPATHY", "spastic paraplegia 10 with or without peripheral neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 10", "shortest_name_length": 5}
{"curie": "MONDO:0044345", "names": ["Manson", "Schistosoma; mansoni", "Schistosomiasis mansoni", "Manson; schistosomiasis", "schistosomiasis; Manson", "SCHISTOSOMIASIS MANSONI", "schistosomiasis mansoni", "Schistosoma mansoni Infection", "Schistosoma mansoni infection", "Schistosoma Mansoni Infection", "Infection, Schistosoma mansoni", "Schistosoma mansoni Infections", "Schistosoma mansonii infection", "Infections, Schistosoma mansoni", "schistosomiasis; Schistosoma mansoni", "Schistosoma mansoni infectious disease", "Schistosoma mansoni disease or disorder", "Schistosoma mansoni infection (disorder)", "Schistosomiasis due to schistosoma mansoni", "Schistosoma mansoni caused disease or disorder", "Schistosomiasis due to Schistosoma mansoni [intestinal schistosomiasis]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Schistosoma mansoni infectious disease", "shortest_name_length": 6}
{"curie": "MONDO:0011965", "names": ["ETL2", "Ftle", "temporal epilepsy, familial", "Temporal epilepsy, familial", "familial temporal lobe epilepsy", "epilepsy, familial temporal lobe", "familial temporal lobe epilepsy 2", "epilepsy, familial temporal lobe, 2", "EPILEPSY, FAMILIAL TEMPORAL LOBE, 2", "familial temporal lobe epilepsy type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial temporal lobe epilepsy 2", "shortest_name_length": 4}
{"curie": "MONDO:0011449", "names": ["SD", "sialuria", "salla disease", "Salla disease", "Salla Disease", "SALLA DISEASE", "Finnish Type Sialuria", "sialuria, Finnish type", "Sialuria, Finnish Type", "Finnish Type Sialurias", "Sialuria, Finnish type", "SIALURIA, FINNISH TYPE", "Sialurias, Finnish Type", "Salla disease (disorder)", "Sialic Acid Storage Disease", "sialic acid storage disease", "Adult sialic acid storage disease", "Sialic Acid Storage Disease, Finnish Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Salla disease", "shortest_name_length": 2}
{"curie": "UMLS:C4524839", "names": ["HEAD NECK CANCER SQUAMOUS CELL RECURRENT", "Recurrent Head and Neck Squamous Cell Cancer", "Recurrent Head and Neck Squamous Cell Carcinoma", "Recurrent Squamous Cell Carcinoma of the Head and Neck"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Head and Neck Squamous Cell Carcinoma", "shortest_name_length": 40}
{"curie": "UMLS:C0346323", "names": ["Malignant Optic Nerve Tumor", "Optic Nerve Tumor, Malignant", "Tumor, Optic Nerve, Malignant", "Tumor, Malignant, Optic Nerve", "Malignant Optic Nerve Neoplasm", "Malignant tumor of optic nerve", "Malignant tumour of optic nerve", "Malignant neoplasm of optic nerve", "Malignant tumor of optic nerve (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant tumor of optic nerve", "shortest_name_length": 27}
{"curie": "MONDO:0033092", "names": ["ARCI13", "autosomal recessive congenital ichthyosis 13", "ichthyosis, congenital, autosomal recessive 13", "ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 13"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ichthyosis, congenital, autosomal recessive 13", "shortest_name_length": 6}
{"curie": "UMLS:C1368821", "names": ["Sclerosing Stromal Tumor", "Ovarian Sclerosing Stromal Tumor", "Sclerosing Stromal Tumor of Ovary", "Ovarian Sclerosing Stromal Neoplasm", "Sclerosing Stromal Neoplasm of Ovary", "Sclerosing Stromal Tumor of the Ovary", "Sclerosing Stromal Neoplasm of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Sclerosing Stromal Tumor", "shortest_name_length": 24}
{"curie": "UMLS:C0700031", "names": ["attack anxiety", "Anxiety attack", "ANXIETY ATTACK", "anxiety attack", "Anxiety attacks", "anxiety attacks", "Attack(s);anxiety", "anxiety attacking", "Anxiety attack (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anxiety attack", "shortest_name_length": 14}
{"curie": "MONDO:0009912", "names": ["PRL deficiency with obesity and enlarged testes", "PRL DEFICIENCY WITH OBESITY AND ENLARGED TESTES", "Prolactin Deficiency with Obesity and Enlarged Testes", "prolactin deficiency with obesity and enlarged testes", "PROLACTIN DEFICIENCY WITH OBESITY AND ENLARGED TESTES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prolactin deficiency with obesity and enlarged testes", "shortest_name_length": 47}
{"curie": "MONDO:0010329", "names": ["MRX77", "XLID77", "X-linked mental retardation 77", "MENTAL RETARDATION, X-LINKED 77", "Mental Retardation, X-Linked 77", "mental retardation, X-linked 77", "intellectual disability, X-linked 77", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 77", "non-syndromic X-linked intellectual disability 77", "mental retardation, X-linked 77, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 77", "shortest_name_length": 5}
{"curie": "MONDO:0016078", "names": ["congenital systemic arteriovenous fistula"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital systemic arteriovenous fistula", "shortest_name_length": 41}
{"curie": "UMLS:C4524740", "names": ["Pathologic Stage IV Gastroesophageal Junction Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IV Gastroesophageal Junction Adenocarcinoma AJCC v8", "shortest_name_length": 68}
{"curie": "UMLS:C5237269", "names": ["Locally Advanced Laryngeal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Laryngeal Carcinoma", "shortest_name_length": 36}
{"curie": "MONDO:0045016", "names": ["cholesterol catabolism disease", "disorder of cholesterol catabolism", "Disorder of cholesterol catabolism", "cholesterol catabolic process disease", "disorder of cholesterol catabolic process", "Disorder of cholesterol catabolism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholesterol catabolic process disease", "shortest_name_length": 30}
{"curie": "MONDO:0032914", "names": ["CILD44", "primary ciliary dyskinesia 44", "CILIARY DYSKINESIA, PRIMARY, 44", "ciliary dyskinesia, primary, 44", "primary ciliary dyskinesia 44 without situs inversus", "CILIARY DYSKINESIA, PRIMARY, 44, WITHOUT SITUS INVERSUS", "Ciliary Dyskinesia, Primary, 44, Without Situs Inversus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ciliary dyskinesia, primary, 44", "shortest_name_length": 6}
{"curie": "MONDO:0020853", "names": ["MERS", "MMERV", "Encephalitis/encephalopathy, mild, with reversible splenial lesion", "ENCEPHALITIS/ENCEPHALOPATHY, MILD, WITH REVERSIBLE SPLENIAL LESION", "ENCEPHALITIS/ENCEPHALOPATHY, MILD, WITH REVERSIBLE MYELIN VACUOLIZATION", "encephalitis/encephalopathy, mild, with reversible myelin vacuolization"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephalitis/encephalopathy, mild, with reversible myelin vacuolization", "shortest_name_length": 4}
{"curie": "MONDO:0011803", "names": ["SPG7", "Spastic Paraplegia 7", "spastic paraplegia 7", "Spastic paraplegia type 7", "spastic paraplegia type 7", "Spastic Paraplegia Type 7", "hereditary spastic paraplegia 7", "SPG7 hereditary spastic paraplegia", "hereditary spastic paraplegia type 7", "Spastic paraplegia type 7 (disorder)", "autosomal recessive spastic paraplegia 7", "Spastic Paraplegia 7, Autosomal Recessive", "spastic paraplegia 7, autosomal recessive", "SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE", "hereditary spastic paraplegia paraplegin type", "Hereditary Spastic Paraplegia, Paraplegin Type", "hereditary spastic paraplegia caused by mutation in SPG7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 7", "shortest_name_length": 4}
{"curie": "MONDO:0014753", "names": ["autosomal recessive optic atrophy", "autosomal recessive isolated optic atrophy", "autosomal recessive nonsyndromic optic atrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive optic atrophy", "shortest_name_length": 33}
{"curie": "MONDO:0054869", "names": ["NDM", "Nondystrophic myotonia", "nondystrophic myotonia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nondystrophic myotonia", "shortest_name_length": 3}
{"curie": "UMLS:C0334355", "names": ["Serous borderline tumor", "Serous borderline tumour", "Borderline Serous Cystadenoma", "Atypical proliferating serous tumor", "Atypical proliferating serous tumour", "Serous tumor, atypical proliferative", "Serous tumour, atypical proliferative", "Serous tumor of low malignant potential", "Borderline Malignancy Serous Cystadenoma", "Serous tumour of low malignant potential", "Serous cystadenoma, borderline malignancy", "Serous cystadenoma - borderline malignancy", "Low Malignancy Potential Serous Cystadenoma", "Serous tumor, NOS, of low malignant potential", "[M] Serous cystadenoma, borderline malignancy", "Serous Tumor of Borderline Malignant Potential", "Serous tumour, NOS, of low malignant potential", "Serous cystadenoma, borderline malignancy (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Serous cystadenoma, borderline malignancy", "shortest_name_length": 23}
{"curie": "MONDO:0011049", "names": ["Aymé-Gripp syndrome", "Fine Lubinsky syndrome", "FINE-LUBINSKY SYNDROME", "Fine-Lubinsky syndrome", "fine-Lubinsky syndrome", "Fine Lubinsky syndrome (disorder)", "Fine Lubinsky syndrome (diagnosis)", "brachycephaly, deafness, cataract and mental retardation", "Brachycephaly, deafness, cataract and mental retardation", "brachycephaly, deafness, cataract and intellectual disability", "Brachycephaly-deafness-cataract-intellectual disability syndrome", "brachycephaly-deafness-cataract-intellectual disability syndrome", "Brachycephaly, deafness, cataract, intellectual disability syndrome", "Brachycephaly-hearing loss-cataract-intellectual disability syndrome", "Brachycephaly, Deafness, Cataract, Microstomia, And Mental Retardation", "BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION", "brachycephaly, deafness, cataract, microstomia, and mental retardation", "brachycephaly-deafness-cataract-microstomia-mental retardation syndrome", "brachycephaly, deafness, cataract, microstomia, and intellectual disability", "BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND IMPAIRED INTELLECTUAL DEVELOPMENT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fine-Lubinsky syndrome", "shortest_name_length": 19}
{"curie": "UMLS:C0334637", "names": ["CB/CC", "Germinoblastoma, diffuse", "Diffuse Centroblastic-Centrocytic Lymphoma", "diffuse centroblastic-centrocytic lymphoma", "Malignant lymphoma, centroblasticcentrocytic, NOS", "Malignant lymphoma, centroblastic-centrocytic, NOS", "Malignant lymphoma, centroblastic-centrocytic, diffuse", "Diffuse malignant lymphoma - centroblastic-centrocytic", "diffuse centroblastic-centrocytic lymphoma (diagnosis)", "[M]Malignant lymphoma, centroblastic-centrocytic, diffuse", "Diffuse malignant lymphoma - centroblastic-centrocytic (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse malignant lymphoma - centroblastic-centrocytic", "shortest_name_length": 5}
{"curie": "MONDO:0013926", "names": ["HH14", "WDR11 hypogonadotropic hypogonadism", "hypogonadotropic hypogonadism 14 with or without anosmia", "HYPOGONADOTROPIC HYPOGONADISM 14 WITH OR WITHOUT ANOSMIA", "hypogonadotropic hypogonadism caused by mutation in WDR11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadotropic hypogonadism 14 with or without anosmia", "shortest_name_length": 4}
{"curie": "UMLS:C1335358", "names": ["Parotid Angioma", "Angioma of Parotid", "Parotid Hemangioma", "Parotid Gland Angioma", "Hemangioma of Parotid", "Angioma of the Parotid", "Parotid Gland Hemangioma", "Angioma of Parotid Gland", "Hemangioma of the Parotid", "Hemangioma of Parotid Gland", "Angioma of the Parotid Gland", "Hemangioma of the Parotid Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parotid Gland Hemangioma", "shortest_name_length": 15}
{"curie": "MONDO:0009962", "names": ["SLSN", "SLSN1", "LOKEN-SENIOR SYNDROME", "SENIOR-LOKEN SYNDROME", "Senior-Løken Syndrome", "Loken Senior syndrome", "Loken-Senior syndrome", "Senior-Loken Syndrome", "Senior-Loken syndrome", "Loken-Senior Syndrome", "Senior Loken Syndrome", "Renal-retinal syndrome", "RENAL-RETINAL SYNDROME", "renal-retinal syndrome", "senior-loken syndrome-1", "Senior-Loken Syndrome 1", "SENIOR-Loken syndrome 1", "Senior-Loken syndrome 1", "SENIOR-LOKEN SYNDROME 1", "NPHP1 Senior-Loken syndrome", "Senior-Loken syndrome type 1", "Renal dysplasia retinal aplasia", "Renal Dysplasia And Retinal Aplasia", "RENAL DYSPLASIA AND RETINAL APLASIA", "renal dysplasia and retinal aplasia", "Renal dysplasia and retinal aplasia", "Nephronophthisis with retinal dystrophy", "Renal dysplasia-retinal aplasia syndrome", "juvenile nephronophthisis with Leber amaurosis", "Juvenile nephronophthisis with Leber amaurosis", "Renal dysplasia and retinal aplasia (disorder)", "JUVENILE NEPHRONOPHTHISIS WITH LEBER AMAUROSIS", "Senior-Loken syndrome caused by mutation in NPHP1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Senior-Loken syndrome 1", "shortest_name_length": 4}
{"curie": "MONDO:0016108", "names": ["autosomal dominant distal myopathy", "distal myopathy, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant distal myopathy", "shortest_name_length": 34}
{"curie": "UMLS:C0853857", "names": ["Cellulitis staphylococcal", "Staphylococcal cellulitis", "Cellulitis caused by Staphylococcus aureus", "Cellulitis caused by Staphylococcus aureus (disorder)", "Cellulitis caused by Staphylococcus aureus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cellulitis caused by Staphylococcus aureus", "shortest_name_length": 25}
{"curie": "MONDO:0017915", "names": ["pure or complex autosomal recessive spastic paraplegia", "Pure or complicated autosomal recessive spastic paraplegia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pure or complex autosomal recessive spastic paraplegia", "shortest_name_length": 54}
{"curie": "MONDO:0020585", "names": ["Anemia due to Erythrocyte Enzyme Disorder", "anemia due to erythrocyte enzyme disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anemia due to erythrocyte enzyme disorder", "shortest_name_length": 41}
{"curie": "MONDO:0100349", "names": ["JS-H", "COACH SYNDROME", "COACH syndrome", "gentile syndrome", "Gentile syndrome", "Joubert syndrome with hepatic defect", "JOUBERT SYNDROME WITH CONGENITAL HEPATIC FIBROSIS", "Joubert syndrome with congenital hepatic fibrosis", "Joubert syndrome with congenital hepatic fibrosis (disorder)", "cerebellar vermis hypoplasia-oligophrenia-congenital ataxia-coloboma-hepatic fibrosis", "Cerebellar vermis hypoplasia-oligophrenia-congenital ataxia-coloboma-hepatic fibrosis", "Cerebellar vermis hypoplasia, oligophrenia, congenital ataxia, coloboma, hepatic fibrosis", "cerebellar vermis hypo/aplasia, oligophrenia, ataxia congenital, coloboma, and hepatic fibrosis", "Cerebellar vermis hypo-aplasia, Oligophrenia, Ataxia congenital, Coloboma, and Hepatic fibrosis", "CEREBELLAR VERMIS HYPO/APLASIA, OLIGOPHRENIA, CONGENITAL ATAXIA, OCULAR COLOBOMA, AND HEPATIC FIBROSIS", "Cerebellar Vermis Hypo-Aplasia, Oligophrenia, Congenital Ataxia, Ocular Coloboma, And Hepatic Fibrosis", "cerebellar vermis hypo/aplasia, oligophrenia, congenital ataxia, ocular coloboma, and hepatic fibrosis", "COACH (cerebellar vermis hypoplasia, oligophrenia, congenital ataxia, coloboma, hepatic fibrosis) syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "COACH syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0341016", "names": ["Streptococcal stomatitis", "Streptococcal infection of mouth", "Streptococcal infection of mouth (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Streptococcal infection of mouth", "shortest_name_length": 24}
{"curie": "UMLS:C1266156", "names": ["Cystic Mesothelioma", "Multicystic Mesothelioma", "Intermediate Mesothelioma", "Cystic mesothelioma, benign", "Multicystic mesothelioma, benign", "Multicystic mesothelioma, benign (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Multicystic mesothelioma, benign", "shortest_name_length": 19}
{"curie": "MONDO:0010461", "names": ["MRXSN", "MRXS30", "mental retardation, X-linked, syndromic 30", "MENTAL RETARDATION, X-LINKED, SYNDROMIC 30", "intellectual disability, X-linked, syndromic 30", "X-linked intellectual disability, Nascimento type", "mental retardation, X-linked syndromic, Nascimento-type", "mental retardation, X-linked, syndromic, Nascimento type", "MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE", "syndromic X-linked intellectual disability Nascimento type", "intellectual disability, X-linked syndromic, Nascimento-type", "intellectual disability, X-linked, syndromic, Nascimento type", "X-linked intellectual disability-nail dystrophy-seizures syndrome", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, NASCIMENTO TYPE", "intellectual developmental disorder, X-linked syndromic, Nascimento type, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic X-linked intellectual disability Nascimento type", "shortest_name_length": 5}
{"curie": "UMLS:C4744990", "names": ["Advanced Small Intestinal Large Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Small Intestinal Large Cell Neuroendocrine Carcinoma", "shortest_name_length": 61}
{"curie": "UMLS:C4727502", "names": ["Unresectable Gastric Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Gastric Adenocarcinoma", "shortest_name_length": 35}
{"curie": "MONDO:0014481", "names": ["NISBD2", "INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 2", "inflammatory skin and bowel disease, neonatal, 2", "EGFR neonatal inflammatory skin and bowel disease", "inflammatory skin and bowel disease, neonatal, type 2", "neonatal inflammatory skin and bowel disease caused by mutation in EGFR"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory skin and bowel disease, neonatal, 2", "shortest_name_length": 6}
{"curie": "MONDO:0054791", "names": ["HLD16", "hypomyelinating leukodystrophy 16", "LEUKODYSTROPHY, HYPOMYELINATING, 16", "leukodystrophy, hypomyelinating, 16"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukodystrophy, hypomyelinating, 16", "shortest_name_length": 5}
{"curie": "MONDO:0009650", "names": ["ICD", "ML 2", "GNPTA", "ML II", "Leroy disease", "LEROY DISEASE", "I-CELL DISEASE", "I-cell disease", "I-Cell Disease", "i-cell disease", "i cell disease", "I cell disease", "cell disease i", "I Cell Disease", "I-Cell Diseases", "mucolipidosis 2", "I-cell; disease", "Mucolipidosis 2", "ML 2 Alpha/Beta", "Mucolipidosis II", "mucolipidosis ii", "mucolipidosis II", "ML II ALPHA/BETA", "MUCOLIPIDOSIS II", "mucolipidosis; II", "II; mucolipidosis", "ML disorder type 2", "Mucolipidosis type II", "Mucolipidosis Type II", "mucolipidosis type ii", "mucolipidosis type II", "Type II Mucolipidosis", "Type II Mucolipidoses", "Mucolipidoses, Type II", "Mucolipidosis, Type II", "inclusion cell disease", "inclusion-cell disease", "INCLUSION CELL DISEASE", "Mucolipidosis, type II", "Inclusion-cell Disease", "Inclusion Cell Disease", "Inclusion Cell Diseases", "I-cell disease (disorder)", "mucolipidosis 2 alpha/beta", "I-cell disease (diagnosis)", "MUCOLIPIDOSIS II ALPHA/BETA", "Mucolipidosis II Alpha Beta", "mucolipidosis II alpha/beta", "cell disease i cell inclusion", "disease (or disorder); I-cell", "I-cell - Inclusion cell disease", "Mucolipidosis type II alpha/beta", "mucolipidosis type II alpha/beta", "MUCOLIPIDOSIS II ALPHA/BETA (disorder)", "N-acetylglucosamine 1phosphotransferase deficiency", "N-acetylglucosamine-1-phosphotransferase deficiency", "N-acetylglucosamine 1-phosphotransferase deficiency", "N-Acetylglucosamine-1-phosphotransferase deficiency", "Deficiency of N-acetylglucosamine-1-phosphotransferase"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucolipidosis type II", "shortest_name_length": 3}
{"curie": "UMLS:C1516069", "names": ["Astler-Coller C1 Colorectal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Astler-Coller C1 Colorectal Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0004939", "names": ["hallucinogen dependence", "Hallucinogen Dependence", "Hallucinogen dependence", "dependence; hallucinogenics", "hallucinogenics; dependence", "Dependence on hallucinogens", "Hallucinogen dependence (disorder)", "hallucinogen dependence (diagnosis)", "Hallucinogen dependence, unspecified", "Hallucinogen dependence, unspecified use"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hallucinogen dependence", "shortest_name_length": 23}
{"curie": "MONDO:0023567", "names": ["Kozlowski Brown Hardwick syndrome", "unusual facies, hooked clavicles, 13 pairs of ribs, widened metaphyses, square shaped vertebral bodies and communicating hydrocephalus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kozlowski Brown Hardwick syndrome", "shortest_name_length": 33}
{"curie": "MONDO:0017838", "names": ["SOST", "sclerosteosis", "Sclerosteosis", "SCLEROSTEOSIS 1", "Sclerosteosis (disorder)", "CORTICAL HYPEROSTOSIS WITH SYNDACTYLY", "Cortical Hyperostosis with Syndactyly", "Cortical hyperostosis with syndactyly", "cortical hyperostosis with syndactyly", "cortical hyperostosis-syndactyly syndrome", "Cortical hyperostosis-syndactyly syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sclerosteosis", "shortest_name_length": 4}
{"curie": "MONDO:0000232", "names": ["FISF", "Thai tick typhus", "Flinders Island spotted fever", "Flinders island spotted fever", "Flinders Island Spotted Fever"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Flinders island spotted fever", "shortest_name_length": 4}
{"curie": "MONDO:0003138", "names": ["glomerulonephritis subacute", "subacute glomerulonephritis", "Subacute Glomerulonephritis", "Subacute glomerulonephritis", "Subacute glomerulonephritis syndrome", "Subacute glomerulonephritis (disorder)", "Subacute glomerulonephritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subacute glomerulonephritis", "shortest_name_length": 27}
{"curie": "MONDO:0017109", "names": ["isolated partial cerebellar vermis agenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated partial cerebellar vermis agenesis", "shortest_name_length": 43}
{"curie": "MONDO:0020413", "names": ["Encircling double aortic arch", "encircling double aortic arch", "double aortic arch encircling", "Encircling double aortic arch (disorder)", "Encircling double aortic arch (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encircling double aortic arch", "shortest_name_length": 29}
{"curie": "UMLS:C0264231", "names": ["sinus polyp", "SINUS POLYP", "Sinus polyp", "polyp sinus", "polyps sinus", "polyp; sinus", "sinus; polyp", "Polyp(s);sinus", "Nasal sinus polyp", "Polyp of nasal sinus", "Accessory Sinus Polyp", "Paranasal Sinus Polyp", "Accessory polyp of sinus", "Polyp of accessory sinus", "Polyp of Accessory Sinus", "Polyp of Paranasal Sinus", "Polyp of sinus, accessory", "Polyp of nasal sinus, NOS", "Polyp of the Paranasal Sinus", "Polyp of the Accessory Sinus", "Polyp of accessory sinus, NOS", "Nasal sinus polyp (diagnosis)", "Polyp of nasal sinus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Polyp of nasal sinus", "shortest_name_length": 11}
{"curie": "UMLS:C1279264", "names": ["Genitourinary tract infection", "Genitourinary System Infection", "Genitourinary tract infection NOS", "Infectious disease of genitourinary tract", "Infectious disease of genitourinary system", "Infectious disease of genitourinary system (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infectious disease of genitourinary system", "shortest_name_length": 29}
{"curie": "UMLS:C0751250", "names": ["psychophysiological insomnia", "Psychophysiological Insomnia", "Psychophysiological insomnia", "Insomnia, Psychophysiological", "psychophysiological insomnia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Psychophysiological Insomnia", "shortest_name_length": 28}
{"curie": "MONDO:0005710", "names": ["Composite Lymphoma", "Composite lymphoma", "composite lymphoma", "Composite Lymphomas", "Lymphoma, Composite", "Lymphomas, Composite", "Composite Hodgkin and non-Hodgkin lymphoma", "composite Hodgkin and non-Hodgkin lymphoma", "Composite Hodgkin and non-Hodgkin lymphoma (disorder)", "composite Hodgkin and non-Hodgkin lymphoma (diagnosis)", "Composite Hodgkin and non-Hodgkin lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "composite lymphoma", "shortest_name_length": 18}
{"curie": "MONDO:0024517", "names": ["SWNTS1", "Schwannomatosis 1", "SCHWANNOMATOSIS 1", "schwannomatosis 1", "schwannomatosis, somatic", "schwannomatosis-1, susceptibility to", "Neurilemmomatosis, congenital cutaneous", "neurilemmomatosis, congenital cutaneous", "NEURILEMMOMATOSIS, CONGENITAL CUTANEOUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schwannomatosis 1", "shortest_name_length": 6}
{"curie": "MONDO:0017548", "names": ["humero-radio-ulnar fusion, unilateral", "humero-radio-ulnar synostosis, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "humero-radio-ulnar synostosis, unilateral", "shortest_name_length": 37}
{"curie": "UMLS:C1335660", "names": ["Radiation-Induced Vascular Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radiation-Induced Vascular Disease", "shortest_name_length": 34}
{"curie": "UMLS:C3669122", "names": ["5-Alpha Reductase Deficiency", "Steroid 5-Alpha-Reductase Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "5-Alpha Reductase Deficiency", "shortest_name_length": 28}
{"curie": "MONDO:0018422", "names": ["SPG70", "autosomal recessive spastic paraplegia type 70"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive spastic paraplegia type 70", "shortest_name_length": 5}
{"curie": "MONDO:0021315", "names": ["nasopharynx cancer", "Nasopharynx Cancer", "cancer nasopharynx", "Nasopharynx Cancers", "Cancer, Nasopharynx", "Nasopharynx--Cancer", "Cancers, Nasopharynx", "Cancer of Nasopharynx", "Cancer of nasopharynx", "NASOPHARYNGEAL CANCER", "nasopharyngeal cancer", "cancer nasopharyngeal", "Nasopharyngeal Cancer", "Nasopharyngeal cancer", "cancer of nasopharynx", "Nasopharyngeal Cancers", "Cancer, Nasopharyngeal", "Cancers, Nasopharyngeal", "Cancer of the Nasopharynx", "Nasopharyngeal cancer NOS", "CA - Cancer of nasopharynx", "NASOPHARYNX CANCER MALIGNANT", "Malignant tumor of epipharynx", "Malignant Tumor of Nasopharynx", "Malignant Nasopharyngeal Tumor", "Malignant tumor of nasopharynx", "malignant tumor of nasopharynx", "Malignant tumour of epipharynx", "malignant nasopharynx neoplasm", "malignant nasopharyngeal tumor", "Malignant tumour of nasopharynx", "malignant nasopharyngeal neoplasm", "Malignant neoplasm of nasopharynx", "malignant neoplasm of nasopharynx", "Malignant nasopharyngeal neoplasm", "Malignant Neoplasm of Nasopharynx", "Malignant Nasopharyngeal Neoplasm", "malignant tumor of the nasopharynx", "Malignant tumor of postnasal space", "Malignant Tumor of the Nasopharynx", "Malignant tumour of postnasal space", "malignant neoplasm of the nasopharynx", "Malignant Neoplasm of the Nasopharynx", "Malignant neoplasm of nasopharynx, NOS", "Malignant tumor of nasopharynx (disorder)", "malignant neoplasm of nasopharynx (diagnosis)", "Malignant neoplasm of nasopharynx, unspecified", "Malignant neoplasm of nasopharynx, unspecified site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant tumor of nasopharynx", "shortest_name_length": 18}
{"curie": "MONDO:0010255", "names": ["T1DX", "IDDMX", "Iddmx", "diabetes mellitus, insulin-dependent, X-linked", "TYPE 1 DIABETES MELLITUS, X-LINKED, SUSCEPTIBILITY TO", "INSULIN-DEPENDENT DIABETES MELLITUS, X-LINKED, SUSCEPTIBILITY TO", "insulin-dependent diabetes mellitus, X-linked, susceptibility to", "DIABETES MELLITUS, INSULIN-DEPENDENT, X-LINKED, SUSCEPTIBILITY TO", "diabetes mellitus, insulin-dependent, X-linked, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diabetes mellitus, insulin-dependent, X-linked, susceptibility to", "shortest_name_length": 4}
{"curie": "MONDO:0019094", "names": ["antenatal EBV infection", "Antenatal EBV infection", "congenital EBV infection", "Congenital EBV infection", "Antenatal Epstein-Barr virus infection", "antenatal Epstein-Barr virus infection", "Congenital Epstein-Barr virus infection", "congenital Epstein-Barr virus infection", "Congenital infection caused by Epstein-Barr virus", "Congenital infection caused by Human herpesvirus 4", "Mother-to-child transmission of Epstein-Barr virus infection", "Congenital infection caused by Epstein-Barr virus (disorder)", "mother-to-child transmission of Epstein-Barr virus infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital Epstein-Barr virus infection", "shortest_name_length": 23}
{"curie": "UMLS:C5235848", "names": ["Locally Advanced Parathyroid Gland Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Parathyroid Gland Carcinoma", "shortest_name_length": 44}
{"curie": "MONDO:0008186", "names": ["PANCYTOPENIA AND OCCLUSIVE VASCULAR DISEASE", "pancytopenia and occlusive vascular disease", "Pancytopenia and Occlusive Vascular Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancytopenia and occlusive vascular disease", "shortest_name_length": 43}
{"curie": "MONDO:0002954", "names": ["multifocal basal cell carcinoma", "Multifocal basal cell carcinoma", "basal cell carcinoma superficial", "Superficial basal cell carcinoma", "superficial basal cell carcinoma", "Superficial Basal Cell Carcinoma", "Multicentric Basal Cell Carcinoma", "Multicentric basal cell carcinoma", "multicentric basal cell carcinoma", "Superficial basal cell carcinoma (disorder)", "multifocal superficial basal cell carcinoma", "superficial multifocal basal cell carcinoma", "Superficial Multifocal Basal Cell Carcinoma", "Multifocal superficial basal cell carcinoma", "Superficial basal cell carcinoma (diagnosis)", "Superficial multicentric basal-cell carcinoma", "superficial multicentric basal-cell carcinoma", "skin neoplasm malignant carcinoma basal cell superficial", "Multifocal superficial basal cell carcinoma (morphologic abnormality)", "multifocal superficial basal cell carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "superficial multifocal basal cell carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0600026", "names": ["VLS", "vanishing lung syndrome", "idiopathic giant bullous emphysema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vanishing lung syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0015518", "names": ["SNDI", "IBSN", "Striatal degeneration familial", "familial striatal degeneration", "striatal degeneration familial", "Striatal Degeneration, Familial", "STRIATAL DEGENERATION, FAMILIAL", "infantile striatonigral necrosis", "Infantile striatonigral necrosis", "Infantile striatonigral degeneration", "infantile striatonigral degeneration", "striatonigral degeneration infantile", "Striatonigral degeneration infantile", "INFANTILE BILATERAL STRIATAL NECROSIS", "Striatonigral Degeneration, Infantile", "infantile bilateral striatal necrosis", "Infantile bilateral striatal necrosis", "STRIATONIGRAL DEGENERATION, INFANTILE", "BILATERAL STRIATAL NECROSIS, INFANTILE", "Bilateral Striatal Necrosis, Infantile", "infantile bilateral striatal necrosis syndrome", "Infantile striatonigral degeneration (disorder)", "infantile bilateral striatal necrosis (IBSN) syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile bilateral striatal necrosis", "shortest_name_length": 4}
{"curie": "MONDO:0018130", "names": ["brain dopamine-serotonin vesicular transport disease", "Brain dopamine-serotonin vesicular transport disease", "Brain dopamine-serotonin vesicular transport disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brain dopamine-serotonin vesicular transport disease", "shortest_name_length": 52}
{"curie": "MONDO:0016489", "names": ["HPFH", "HBFQTL1", "F thalassemia", "F thalassaemia", "delta-beta thalassemia", "Delta-beta thalassemia", "DELTA-BETA THALASSEMIA", "delta-beta-thalassemia", "delta-beta Thalassemia", "Delta-Beta Thalassemia", "DELTA/BETA THALASSEMIA", "Delta-beta-thalassemia", "Delta beta thalassemia", "delta beta-thalassemia", "thalassemia; delta-beta", "Delta beta thalassaemia", "delta-beta; thalassemia", "Delta-beta thalassaemia", "delta beta thalassaemia", "Delta Beta 0 Thalassemia", "Hb delta beta0 Thalassemia", "delta beta Thalassemia, NOS", "Delta beta thalassemia (disorder)", "HEMOGLOBIN F, HEREDITARY PERSISTENCE OF", "FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 1", "HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN, HB GENE CLUSTER-RELATED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "delta-beta-thalassemia", "shortest_name_length": 4}
{"curie": "MONDO:0014614", "names": ["CSNB1G", "congenital stationary night blindness 1G", "congenital stationary night blindness type 1G", "night blindness, congenital stationary, type 1G", "NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1G"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital stationary night blindness 1G", "shortest_name_length": 6}
{"curie": "DOID:0060164", "names": ["pain disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pain disorder", "shortest_name_length": 13}
{"curie": "MONDO:0010322", "names": ["MRX2", "XLID2", "X-linked mental retardation 2", "Mental Retardation, X-Linked 2", "MENTAL RETARDATION, X-LINKED 2", "mental retardation, X-linked 2", "intellectual disability, X-linked 2", "X-linked mental retardation 2 (MRX2, XLMR2)", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 2", "non-syndromic X-linked intellectual disability 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 2", "shortest_name_length": 4}
{"curie": "MONDO:0042967", "names": ["mitral valve diseases", "Diseases of mitral valve", "Rheumatic mitral valve disease", "rheumatic mitral valve disease", "Rheumatic mitral valve changes", "rheumatic valve mitral disease", "rheumatic mitral valve changes", "rheumatic mitral valve disorder", "Rheumatic mitral valve diseases", "mitral valve disorder rheumatic", "Mitral valve disease, unspecified", "mitral valve; disorder, rheumatic", "rheumatic disease of mitral valve", "Rheumatic disease of mitral valve", "mitral valve rheumatologic disorder", "Rheumatic disease of mitral valve, NOS", "rheumatologic disorder of mitral valve", "rheumatic mitral valve disorder (diagnosis)", "Rheumatic disease of mitral valve (disorder)", "Rheumatic mitral (valve) disorder (chronic) NOS", "disease (or disorder); mitral(valve) (rheumatic)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rheumatic disease of mitral valve", "shortest_name_length": 21}
{"curie": "MONDO:0001953", "names": ["PYURIA", "Pyuria", "pyuria", "Pyurias", "urine WBC", "pus urine", "pus; urine", "urine; pus", "pus in urine", "leukocyturia", "Leukocyturia", "Pus in urine", "cell pus urine", "URINE PURULENT", "Urine purulent", "urine leukocyte", "leukocyte urine", "cells pus urine", "reported pyuria", "leucocyte urine", "pyuria (disease)", "leucocytes urine", "leukocytes urine", "urine leukocytes", "Pyuria (finding)", "URINE LEUKOCYTES", "purulent; urinary", "pus cells in urine", "Pus cells in urine", "Urine WBC increased", "Leucocytes in urine", "leucocytes in urine", "leukocytes in urine", "Leukocytes in urine", "URINE WBC INCREASED", "in urine leukocytes", "URINE CONTAINING PUS", "Urine containing pus", "pus in urine (symptom)", "urinalysis results: WBC", "URINE LEUKOCYTES INCREASED", "urine leukocytes (lab test)", "High urine neutrophil count", "Pus cells in urine (finding)", "Urine Microscopy: white cells", "Leukocytes in urine (finding)", "urinalysis results: leukocyte", "Urine micr.:leucocytes present", "Urine micr.:leukocytes present", "the urine contains pus (pyuria)", "White blood cells urine positive", "Urine white blood cell increased", "URINE WHITE BLOOD CELLS INCREASED", "White blood cells urine increased", "Urine microscopy: leukocytes present", "Urine microscopy: leucocytes present", "Urine microscopy: white cells present", "Urine microscopy: leukocytes present (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyuria", "shortest_name_length": 6}
{"curie": "MONDO:0007656", "names": ["GSD", "GSS", "GSS syndrome", "PRION DEMENTIA", "prion dementia", "Prion Dementia", "GERSTMANN-STRAUSSLER DISEASE", "Gerstmann-Straussler Disease", "Gerstmann Straussler Disease", "Gerstmann-Straussler disease", "Disease, Gerstmann-Straussler", "Gerstmann Straussler syndrome", "Gerstmann-Straussler Syndrome", "Gerstmann Straussler Syndrome", "Gerstmann-Straussler Diseases", "Diseases, Gerstmann-Straussler", "Gerstmann-Straussler-Scheinker disease", "GERSTMANN-STRAUSSLER-SCHEINKER DISEASE", "Gerstmann Straussler Scheinker Disease", "Gerstmann-Straussler-Scheinker Disease", "Gerstmann-Sträussler-Scheinker syndrome", "Gerstmann Straussler Scheinker syndrome", "Gerstmann-Straussler-Scheinker syndrome", "Gerstmann-Straussler-Scheinker Syndrome", "Gerstmann Straussler Scheinker Syndrome", "Gerstmann-Straeussler-Scheinker syndrome", "CEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED", "cerebral amyloid angiopathy, Prnp-related", "GSS - Gerstmann-Straussler-Scheinker syndrome", "Gerstmann-Straussler-Scheinker syndrome (disorder)", "Gerstmann-Straussler-Scheinker syndrome (diagnosis)", "amyloidosis cerebral with spongiform encephalopathy", "amyloidosis, cerebral, with spongiform encephalopathy", "AMYLOIDOSIS, CEREBRAL, WITH SPONGIFORM ENCEPHALOPATHY", "Amyloidosis, Cerebral, with Spongiform Encephalopathy", "Gerstmann Straussler Inherited Spongiform Encephalopathy", "Gerstmann-Straussler Inherited Spongiform Encephalopathy", "Inherited Spongiform Encephalopathy, Gerstmann-Straussler", "Inherited Spongiform Encephalopathy, Gerstmann Straussler", "encephalopathy subacute spongiform Gerstmann-Straussler type", "subacute spongiform encephalopathy, Gerstmann-Straussler type", "Subacute spongiform encephalopathy, Gerstmann-Straussler type", "ENCEPHALOPATHY, SUBACUTE SPONGIFORM, GERSTMANN-STRAUSSLER TYPE", "Encephalopathy, Subacute Spongiform, Gerstmann-Straussler Type", "encephalopathy, Subacute spongiform, Gerstmann-Straussler type", "Cerebellar Ataxia, Progressive Dementia, and Amyloid Deposits In CNS", "cerebellar ataxia, progressive dementia, and amyloid deposits in CNS", "CEREBELLAR ATAXIA, PROGRESSIVE DEMENTIA, AND AMYLOID DEPOSITS IN CNS", "cerebellar ataxia, progressive dementia, and amyloid deposits in the central nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gerstmann-Straussler-Scheinker syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C1571984", "names": ["Involutional Psychoses", "Involutional Psychosis", "Psychoses, Involutional", "Psychosis, Involutional"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Psychosis, Involutional", "shortest_name_length": 22}
{"curie": "MONDO:0032797", "names": ["MYOTREM", "MYOGENIC TREMOR", "Myogenic Tremor", "congenital myopathy 16", "MYOPATHY, CONGENITAL, WITH TREMOR", "myopathy, congenital, with tremor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy, congenital, with tremor", "shortest_name_length": 7}
{"curie": "UMLS:C0020452", "names": ["HYPEREMIA", "Hyperemia", "hyperemia", "hyperaemia", "Hyperaemia", "Hyperemias", "HYPERAEMIA", "engorgement", "Engorgement", "Engorgements", "Hyperemia, NOS", "Hyperaemia, NOS", "Local congestion", "Engorgement, NOS", "Vascular engorgement", "Hyperemia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyperemia", "shortest_name_length": 9}
{"curie": "MONDO:0017743", "names": ["disorder of O-N-acetylgalactosaminylglycan synthesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of O-N-acetylgalactosaminylglycan synthesis", "shortest_name_length": 52}
{"curie": "UMLS:C1336221", "names": ["fallopian tube cancer stage IIIB", "Fallopian Tube Cancer Stage IIIB", "stage IIIB fallopian tube cancer", "Stage IIIB Fallopian Tube Cancer", "AJCC stage IIIB fallopian tube cancer", "AJCC Stage IIIB Fallopian Tube Cancer", "Stage IIIB Fallopian Tube Cancer AJCC v7", "FIGO stage IIIB fallopian tube carcinoma", "stage IIIB fallopian tube cancer AJCC v7", "FIGO Stage IIIB Fallopian Tube Carcinoma", "FIGO stage IIIB carcinoma of fallopian tube", "FIGO Stage IIIB Carcinoma of Fallopian Tube", "FIGO stage IIIB carcinoma of the fallopian tube", "FIGO Stage IIIB Carcinoma of the Fallopian Tube"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Fallopian Tube Cancer AJCC v7", "shortest_name_length": 32}
{"curie": "MONDO:0016610", "names": ["idiopathic eosinophilic myositis", "idiopathic eosinophilia-associated myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic eosinophilic myositis", "shortest_name_length": 32}
{"curie": "MONDO:0044880", "names": ["cystic tumor of the pancreas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cystic tumor of the pancreas", "shortest_name_length": 28}
{"curie": "MONDO:0024228", "names": ["Mamillaria", "Miliaria profunda", "miliaria profunda", "profunda; miliaria", "miliaria; profunda", "Miliaria profunda (disorder)", "miliaria profunda (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "miliaria profunda", "shortest_name_length": 10}
{"curie": "MONDO:0015011", "names": ["OPA11", "optic atrophy 11", "OPTIC ATROPHY 11", "optic atrophy type 11", "YME1L1 autosomal recessive isolated optic atrophy", "autosomal recessive isolated optic atrophy caused by mutation in YME1L1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "optic atrophy 11", "shortest_name_length": 5}
{"curie": "MONDO:0012430", "names": ["CAMRQ2", "WDR81 dysequilibrium syndrome", "dysequilibrium syndrome caused by mutation in WDR81", "CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 2", "Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2", "cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2", "cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 2", "cerebellar ataxia, mental retardation, and dysequilibrium syndrome type 2", "cerebellar ataxia, intellectual disability, and dysequilibrium syndrome type 2", "cerebellar ataxia and mental retardation with or without quadrupedal locomotion 2", "CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDAL LOCOMOTION 2", "Cerebellar Ataxia And Mental Retardation With Or Without Quadrupedal Locomotion 2", "CEREBELLAR ATAXIA, IMPAIRED INTELLECTUAL DEVELOPMENT, AND DYSEQUILIBRIUM SYNDROME 2", "cerebellar ataxia and intellectual disability with or without quadrupedal locomotion 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 2", "shortest_name_length": 6}
{"curie": "MONDO:0002055", "names": ["Breast Spiradenoma", "Benign Breast Eccrine Spiradenoma", "benign eccrine breast spiradenoma", "Benign Eccrine Breast Spiradenoma", "benign breast eccrine spiradenoma", "Benign Eccrine Spiradenoma of Breast", "benign eccrine spiradenoma of breast", "Benign Eccrine Spiradenoma of the Breast", "benign eccrine spiradenoma of the breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign eccrine breast spiradenoma", "shortest_name_length": 18}
{"curie": "UMLS:C2981623", "names": ["Stage 0 Intrahepatic Cholangiocarcinoma AJCC v7", "Stage 0 Intrahepatic Bile Duct Cancer (Cholangiocarcinoma)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Intrahepatic Cholangiocarcinoma AJCC v7", "shortest_name_length": 47}
{"curie": "UMLS:C1275317", "names": ["anaplastic large T-cell systemic lymphoma", "Anaplastic large T-cell systemic malignant lymphoma", "anaplastic large T-cell systemic lymphoma (diagnosis)", "Anaplastic large T-cell systemic malignant lymphoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anaplastic large T-cell systemic malignant lymphoma", "shortest_name_length": 41}
{"curie": "MONDO:0016331", "names": ["Infantile systemic hyalinosis", "infantile systemic hyalinosis", "Infantile systemic hyalinosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile systemic hyalinosis", "shortest_name_length": 29}
{"curie": "MONDO:0013542", "names": ["MYMY5", "Moyamoya disease 5", "MOYAMOYA DISEASE 5", "ACTA2 Moyamoya disease", "Moyamoya disease type 5", "Moyamoya disease caused by mutation in ACTA2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Moyamoya disease 5", "shortest_name_length": 5}
{"curie": "MONDO:0024193", "names": ["portal hypertension, noncirrhotic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "portal hypertension, noncirrhotic", "shortest_name_length": 33}
{"curie": "MONDO:0006267", "names": ["Liver Cavernous Hemangioma", "liver cavernous hemangioma", "Cavernous hemangioma of liver", "cavernous hemangioma of liver", "Cavernous haemangioma of liver", "Cavernous hemangioma of liver (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "liver cavernous hemangioma", "shortest_name_length": 26}
{"curie": "MONDO:0008994", "names": ["cleidocranial dysplasia recessive form", "cleidocranial dysplasia, recessive form", "Cleidocranial Dysplasia, Recessive Form", "CLEIDOCRANIAL DYSPLASIA, RECESSIVE FORM", "autosomal recessive form of cleidocranial dysostosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleidocranial dysplasia, recessive form", "shortest_name_length": 38}
{"curie": "MONDO:0020257", "names": ["gaze palsy", "conjugate gaze palsy", "supranuclear ocular palsy", "supranuclear oculomotor palsy", "supranuclear disorder of eye movement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "supranuclear oculomotor palsy", "shortest_name_length": 10}
{"curie": "MONDO:0007243", "names": ["BL", "Burkitt Tumor", "burkitt tumor", "tumor; Burkitt", "Burkitts Tumor", "Burkitt; tumor", "Tumor, Burkitt", "burkitts tumor", "NHL, Burkitt's", "Burkitt's Tumor", "burkitt's tumor", "Burkitt's tumor", "Burkitt lymphoma", "Tumor, Burkitt's", "Burkitt Lymphoma", "Burkitt's tumour", "burkitt lymphoma", "BURKITT LYMPHOMA", "LYMPHOMA BURKITT", "Burkitts Lymphoma", "Burkitt; lymphoma", "LYMPHOMA, BURKITT", "burkitts lymphoma", "Lymphoma, Burkitt", "burkitt lymphomas", "lymphoma; Burkitt", "Burkitts lymphoma", "Burkitt's Lymphoma", "Burkitt's leukemia", "burkitt's lymphoma", "Burkitt's lymphoma", "Lymphoma, Burkitt's", "Burkitt's lymphomas", "Burkitt's leukaemia", "lymphoma, Burkitt's", "Burkitt-like lymphoma", "Burkitt lymphoma, NOS", "Burkitt-like Lymphoma", "Burkitt's lymphoma NOS", "Burkitt's-like Lymphoma", "BL - Burkitt's lymphoma", "Burkitt's lymphoma, NOS", "burkitt lymphoma, somatic", "Burkitt lymphoma/leukemia", "childhood Burkitt lymphoma", "NHL, Burkitt lymphoma (BL)", "Burkitt lymphoma/leukaemia", "Burkitt's tumor or lymphoma", "Burkitt's tumour or lymphoma", "Burkitt's lymphoma (clinical)", "Burkitt's lymphoma (disorder)", "Burkitt's lymphoma - disorder", "Malignant lymphoma, Burkitt's", "Small Noncleaved-Cell Lymphoma", "Small Noncleaved Cell Lymphoma", "Burkitt's lymphoma (diagnosis)", "Small Non-Cleaved-Cell Lymphoma", "Noncleaved-Cell Lymphoma, Small", "Small non-cleaved cell lymphoma", "Lymphoma, Small Noncleaved Cell", "Small Noncleaved-Cell Lymphomas", "Lymphoma, Small Noncleaved-Cell", "Small Non Cleaved Cell Lymphoma", "small non-cleaved cell lymphoma", "Lymphoma, Small Non Cleaved Cell", "Small Non-Cleaved-Cell Lymphomas", "Non-Cleaved-Cell Lymphoma, Small", "Lymphoma, Small Non-Cleaved-Cell", "burkitt's non-hodgkin's lymphoma", "Diffuse Undifferentiated Lymphoma", "non-Hodgkin's lymphoma, Burkitt's", "malignant lymphoma, Burkitt's type", "Lymphoma, Diffuse Undifferentiated", "Burkitt lymphoma, unspecified site", "Undifferentiated Lymphoma, Diffuse", "Malignant lymphoma, Burkitt's type", "Diffuse Undifferentiated Lymphomas", "Lymphoma, Undifferentiated, Diffuse", "Burkitt's tumor non-Hodgkin's lymphoma", "Atypical Burkitt/Burkitt-Like Lymphoma", "Burkitt's tumour non-Hodgkin's lymphoma", "Atypical Burkitt's/Burkitt's-Like Lymphoma", "Burkitt lymphoma (morphologic abnormality)", "Malignant lymphoma, small non-cleaved cell", "Small Non-Cleaved Cell Lymphoma, Burkitt's Type", "small Non-Cleaved cell Lymphoma, Burkitt's type", "lymphoma; undifferentiated cell, Burkitt's type", "small non-cleaved cell lymphoma, Burkitt's type", "Malignant lymphoma, lymphoblastic, Burkitt's type", "Burkitt lymphoma/leukemia (morphologic abnormality)", "Malignant lymphoma, undifferentiated, Burkitt's type", "Burkitt's type malignant lymphoma - undifferentiated", "Burkitt's type malignant lymphoma - small non-cleaved", "Malignant lymphoma, small noncleaved, Burkitt's, diffuse"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Burkitt lymphoma", "shortest_name_length": 2}
{"curie": "MONDO:0019249", "names": ["MPS", "Mucopolysaccharidoses", "Mucopolysaccharidosis", "mucopolysaccharidoses", "mucopolysaccharidosis", "Mucopolysaccharidosis NOS", "Mucopolysaccharidosis, NOS", "MPS - Mucopolysaccharidosis", "Mucopolysaccharidosis (disorder)", "mucopolysaccharidosis (diagnosis)", "Mucopolysaccharidosis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucopolysaccharidosis", "shortest_name_length": 3}
{"curie": "EFO:1001507", "names": ["asparaginase-induced acute pancreatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "asparaginase-induced acute pancreatitis", "shortest_name_length": 39}
{"curie": "UMLS:C0403639", "names": ["Chemical cystitis", "cystitis chemical", "Chemical cystitis (disorder)", "Chemical cystitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chemical cystitis", "shortest_name_length": 17}
{"curie": "UMLS:C4520832", "names": ["Stage 0 Pancreatic Cancer", "Pancreatic Cancer Stage 0", "Pancreatic Carcinoma in Situ", "Stage 0 Pancreatic Carcinoma", "Stage 0 Carcinoma of Pancreas", "Stage 0 Pancreatic Cancer AJCC v6", "Stage 0 Pancreatic Cancer AJCC v7", "Stage 0 Carcinoma of the Pancreas", "stage 0 pancreatic carcinoma in situ", "Stage 0 Pancreatic Cancer AJCC v6 and v7", "Stage 0 Exocrine and Endocrine Pancreatic Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Pancreatic Cancer AJCC v6 and v7", "shortest_name_length": 25}
{"curie": "UMLS:C3900105", "names": ["Combined Hepatocellular Cancer and Cholangiocarcinoma", "Adult Combined Hepatocellular Carcinoma and Cholangiocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Combined Hepatocellular Carcinoma and Cholangiocarcinoma", "shortest_name_length": 53}
{"curie": "MONDO:0020511", "names": ["B-ALL", "B-Cell ALL", "B-precursor ALL", "B-Cell Type Acute Leukemia", "B-cell type acute leukemia", "B-cell lymphoblastic leukemia", "B-Cell Lymphoblastic Leukemia", "B Acute Lymphoblastic Leukemia", "B-Acute Lymphoblastic Leukemia", "B acute lymphoblastic leukemia", "B-cell acute lymphocytic leukemia", "Acute B-Cell Lymphocytic Leukemia", "B-Cell Acute Lymphocytic Leukemia", "B Cell Acute Lymphocytic Leukemia", "B cell acute lymphocytic leukemia", "acute B cell lymphocytic leukemia", "Acute B Cell Lymphocytic Leukemia", "acute B-cell lymphocytic leukemia", "precursor B-lymphoblastic leukemia", "Precursor B-Lymphoblastic Leukemia", "B-Cell Acute Lymphoblastic Leukemia", "B-cell acute lymphoblastic leukemia", "B-Cell Precursor Type Acute Leukemia", "B cell precursor type acute leukemia", "B-cell precursor type acute leukemia", "B Cell Precursor Type Acute Leukemia", "Precursor B-cell lymphoblastic leukemia", "precursor B-cell acute lymphocytic leukemia", "precursor B-cell acute lymphoblastic leukemia", "precursor B-cell acute lymphocytic leukemia/lymphoma", "precursor B-lymphoblastic leukemia (B-precursor ALL)", "Precursor B-lymphoblastic leukemia (B-precursor ALL)", "precursor B-cell acute lymphoblastic leukemia/lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "precursor B-cell acute lymphoblastic leukemia", "shortest_name_length": 5}
{"curie": "UMLS:C1708177", "names": ["Gallbladder Papillary BilIN", "Gallbladder Papillary Intraepithelial Neoplasia", "Gallbladder Papillary Biliary Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gallbladder Papillary Biliary Intraepithelial Neoplasia", "shortest_name_length": 27}
{"curie": "MONDO:0021962", "names": ["Baetz-Greenwalt syndrome", "baetz-greenwalt syndrome", "hypoplastic right-sided heart complex", "Hypoplastic right-sided heart complex"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "baetz-greenwalt syndrome", "shortest_name_length": 24}
{"curie": "UMLS:C0581289", "names": ["Injection site swelling", "injection site swelling", "Swelling at injection site", "Swelling of injection site", "Injection site swelling (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Swelling at injection site", "shortest_name_length": 23}
{"curie": "MONDO:0010004", "names": ["EEC syndrome", "EEC Syndrome", "RUDIGER SYNDROME", "RUDIGER syndrome", "Rudiger's syndrome", "Rudiger syndrome 1", "Walker-Clodius syndrome", "split hand/feet syndrome", "Ectrodactyly-cleft lip-palate syndrome", "ectrodactyly-cleft lip/palate syndrome", "lobster-claw with ectodermal defects syndrome", "ectrodactyly-ectodermal dysplasia-cleft syndrome", "Ectrodactyly-Ectodermal Dysplasia-Cleft Syndrome", "Ectrodactyly-ectodermal dysplasia-clefting syndrome", "ectrodactyly-ectodermal dysplasia-clefting syndrome", "split hand-cleft lip/palate and ectodermal dysplasia", "cleft lip-cleft palate-lobster claw deformity syndrome", "Cleft lip-cleft palate-lobster claw deformity syndrome", "ectrodactyly-ectodermal dysplasia-cleft palate syndrome", "ectrodactyly-ectodermal dysplasia-cleft lip/cleft palate", "ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome", "Ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome", "split hand-cleft lip/palate and ectodermal (SCE) dysplasia", "Ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome", "ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome", "Ectrodactyly-ectodermal dysplasia-clefting syndrome (disorder)", "Ectodermal dysplasia with ectrodactyly and cleft lip or palate", "ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome", "EEC - Ectodermal dysplasia with ectrodactyly and cleft lip or palate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "EEC syndrome", "shortest_name_length": 12}
{"curie": "UMLS:C1516060", "names": ["Astler-Coller B1 Colorectal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Astler-Coller B1 Colorectal Carcinoma", "shortest_name_length": 37}
{"curie": "UMLS:C3536738", "names": ["Lumbar Meningomyelocele", "Lumbar meningomyelocele", "Lumbar Myelomeningocele", "lumbar meningomyelocele", "Lumbar meningomyelocele (disorder)", "lumbar meningomyelocele (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lumbar meningomyelocele", "shortest_name_length": 23}
{"curie": "MONDO:0003362", "names": ["AISMN", "Skin Leiomyosarcoma", "skin leiomyosarcoma", "leiomyosarcoma of skin", "Leiomyosarcoma of Skin", "Cutaneous leiomyosarcoma", "cutaneous leiomyosarcoma", "Cutaneous Leiomyosarcoma", "Leiomyosarcoma of the Skin", "leiomyosarcoma of the skin", "zone of skin leiomyosarcoma", "leiomyosarcoma of zone of skin", "cutaneous leiomyosarcoma (disease)", "leiomyosarcoma of skin (diagnosis)", "Cutaneous leiomyosarcoma (disorder)", "Atypical Intradermal Smooth Muscle Tumor", "Atypical Intradermal Smooth Muscle Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous leiomyosarcoma", "shortest_name_length": 5}
{"curie": "MONDO:0012231", "names": ["CMT2A2", "CMT2A2A", "HMSN2A2", "HMSNIIA2", "HMSN IIA2", "HMSN IIa2", "Charcot-Marie-Tooth Disease Type 2A2", "Charcot-Marie-Tooth disease type 2A2", "Charcot-Marie-Tooth disease Type 2A2", "Charcot-Marie-Tooth Disease Type 2A2A", "Charcot-Marie-Tooth disease type 2A2A", "Charcot-Marie-Tooth neuronal type 2A2", "MFN2 Charcot-Marie-Tooth disease type 2", "Charcot-Marie-Tooth neuropathy type 2A2", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2A2", "Charcot-Marie-Tooth Neuropathy, Type 2A2", "Charcot-Marie-Tooth neuropathy, type 2A2", "Hereditary Motor And Sensory Neuropathy IIA2", "HEREDITARY MOTOR AND SENSORY NEUROPATHY IIA2", "hereditary motor and sensory neuropathy IIA2", "hereditary motor and sensory neuropathy IIa2", "Charcot-Marie-Tooth Disease, Axonal, Type 2A2", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2", "Charcot-Marie-Tooth disease, axonal, type 2A2", "Charcot-Marie-Tooth disease, axonal, type 2A2A", "Charcot-Marie-Tooth Disease, Neuronal, Type 2A2", "Charcot-Marie-Tooth disease, neuronal, type 2A2", "CHARCOT-MARIE-TOOTH DISEASE, NEURONAL, TYPE 2A2", "Charcot-Marie-Tooth disease Type 2A2 (diagnosis)", "autosomal dominant Charcot-Marie-Tooth disease type 2A2", "Autosomal dominant Charcot-Marie-Tooth disease type 2A2", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2 (disorder)", "Charcot-Marie-Tooth disease type 2 caused by mutation in MFN2", "autosomal dominant axonal Charcot-Marie-Tooth disease type 2A2", "Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2A2", "Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2A2", "Autosomal dominant Charcot-Marie-Tooth disease type 2A2 (disorder)", "Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2A2A", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A2A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 2A2", "shortest_name_length": 6}
{"curie": "UMLS:C1333260", "names": ["Primary ameloblastic carcinoma", "De novo Ameloblastic Carcinoma", "Primary Ameloblastic Carcinoma", "Ameloblastic Carcinoma-Primary Type", "Primary ameloblastic carcinoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary ameloblastic carcinoma", "shortest_name_length": 30}
{"curie": "UMLS:C0277565", "names": ["Local", "local disease", "disease local", "Local disease", "Localised disease", "localized disease", "disease localized", "diseases localize", "Localized Disease", "Localized disease", "Local disease, NOS", "Localized disease, NOS", "Local disease (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Local disease", "shortest_name_length": 5}
{"curie": "MONDO:0021396", "names": ["Vulva Polyp", "vulva polyp", "Vulval polyp", "vulvar polyp", "Vulvar Polyp", "vulva; polyp", "polyp; vulva", "Polyp of vulva", "polyp of vulva", "Polyp of Vulva", "polyp of the vulva", "Polyp of the Vulva", "Polyp of vulva, NOS", "mammalian vulva polyp", "vulvar polyp (diagnosis)", "Polyp of vulva (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyp of vulva", "shortest_name_length": 11}
{"curie": "MONDO:0011085", "names": ["NMSL", "CMT4D", "HMSNL", "HMSN4D", "HMSN-Lom", "HMSN Lom type", "HMSN, Lom type", "Charcot-Marie-Tooth disease type 4D", "Charcot-Marie-Tooth disease Type 4D", "Charcot-Marie-Tooth disease, type 4D", "CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D", "Charcot-Marie-Tooth Disease, Type 4D", "Charcot-Marie-Tooth neuropathy type 4D", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4D", "Charcot-Marie-Tooth neuropathy, type 4D", "Charcot-Marie-Tooth Neuropathy, Type 4d", "NDRG1 Charcot-Marie-Tooth disease type 4", "Charcot-Marie-Tooth disease type 4D (disorder)", "Charcot-Marie-Tooth disease Type 4D (diagnosis)", "Hereditary motor and sensory neuropathy Lom type", "hereditary motor and sensory neuropathy LOM type", "hereditary motor ABD sensory neuropathy Lom type", "hereditary motor and sensory neuropathy, Lom type", "Hereditary motor and sensory neuropathy, Lom type", "Hereditary motor and sensory neuropathy, LOM type", "NEUROPATHY, HEREDITARY MOTOR AND SENSORY, LOM TYPE", "neuropathy, hereditary motor and sensory, Lom type", "Neuropathy, hereditary motor and sensory, LOM type", "Charcot-Marie-Tooth disease type 4 caused by mutation in NDRG1", "autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4D", "CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, AUTOSOMAL RECESSIVE, TYPE 4D", "Charcot-Marie-Tooth Disease, Demyelinating, Autosomal Recessive, Type 4d", "Charcot-Marie-Tooth disease, demyelinating, autosomal recessive, type 4D"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 4D", "shortest_name_length": 4}
{"curie": "UMLS:C0280191", "names": ["Recurrent Lymphoblastic Lymphoma", "relapsed adult lymphoblastic lymphoma", "Adult Recurrent Lymphoblastic Lymphoma", "recurrent adult lymphoblastic lymphoma", "Recurrent Adult Lymphoblastic Lymphoma", "adult lymphoblastic lymphoma, relapsed", "adult lymphoblastic lymphoma, recurrent", "lymphoblastic lymphoma, adult, recurrent", "lymphoblastic lymphoma, recurrent, adult", "Recurrent Adult Precursor Lymphoblastic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Adult Lymphoblastic Lymphoma", "shortest_name_length": 32}
{"curie": "UMLS:C1332230", "names": ["Aleukemic Lymphoblastic Leukemia", "Aleukemic Acute Lymphoblastic Leukemia", "Aleukemic Precursor Lymphoblastic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aleukemic Acute Lymphoblastic Leukemia", "shortest_name_length": 32}
{"curie": "MONDO:0009046", "names": ["Fraser", "cyclopism", "Fraser syndrome", "Fraser Syndrome", "fraser syndrome", "FRASER SYNDROME", "Syndrome, Fraser", "Fraser's syndrome", "fraser's syndrome", "Cryptophthalmos syndrome", "cryptophthalmos syndrome", "Fraser-Francois syndrome", "Cryptophthalmos Syndrome", "cryptophthalmos; syndrome", "syndrome; cryptophthalmos", "Ulrich-Feichtiger syndrome", "Fraser syndrome (diagnosis)", "Meyer-Schwickerath's syndrome", "Cryptophthalmos syndrome (disorder)", "CRYPTOPHTHALMOS-SYNDACTYLY SYNDROME", "Cryptophthalmos-Syndactyly Syndrome", "cryptophthalmos-syndactyly syndrome", "Cryptophthalmos-syndactyly syndrome", "Cryptophthalmos Syndactyly Syndrome", "Cryptophthalmos-Syndactyly Syndromes", "cryptophthalmos with other malformations", "Cryptophthalmos with Other Malformations", "CRYPTOPHTHALMOS WITH OTHER MALFORMATIONS", "cryptophthalmos with Other malformations", "congenital deformity of head Fraser syndrome", "Cryptophthalmos, defect of auricle and genital anomaly", "Cryptophthalmos, defect of auricle AND genital anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fraser syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C1518706", "names": ["Ovarian Dermoid Cyst with Secondary Melanocytic Lesion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Dermoid Cyst with Secondary Melanocytic Lesion", "shortest_name_length": 54}
{"curie": "UMLS:C5420147", "names": ["Advanced Lung Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Lung Squamous Cell Carcinoma", "shortest_name_length": 37}
{"curie": "UMLS:C1275515", "names": ["Venomous bite", "venomous; bite", "bite; venomous", "Venomous bite wound", "animal; bite, venomous", "bite; animal, venomous", "Venomous bite wound (disorder)", "Wound from bite of venomous animal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Venomous bite wound", "shortest_name_length": 13}
{"curie": "MONDO:0011216", "names": ["HFE2A", "hemochromatosis, type 2", "hemochromatosis type 2A", "Hemochromatosis, Type 2A", "hemochromatosis, type 2A", "HEMOCHROMATOSIS, TYPE 2A", "hemochromatosis, juvenile", "HJV hemochromatosis type 2", "hemochromatosis type 2 caused by mutation in HJV"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemochromatosis type 2A", "shortest_name_length": 5}
{"curie": "UMLS:C0520893", "names": ["Peeling", "PEELING", "Localised exfoliation", "Localized exfoliation", "Localized desquamation", "Localised desquamation", "Localized desquamation (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized desquamation", "shortest_name_length": 7}
{"curie": "UMLS:C1737223", "names": ["Secondary hypoparathyroidism", "Hypoparathyroidism secondary", "secondary hypoparathyroidism", "Secondary hypoparathyroidism (disorder)", "secondary hypoparathyroidism (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary hypoparathyroidism", "shortest_name_length": 28}
{"curie": "UMLS:C1096460", "names": ["Infusion site phlebitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infusion site phlebitis", "shortest_name_length": 23}
{"curie": "UMLS:C0751712", "names": ["Posterior Ischemic Optic Neuropathy", "Posterior ischemic optic neuropathy", "ischemic optic neuropathy posterior", "Posterior ischaemic optic neuropathy", "Optic Neuropathy, Posterior Ischemic", "PION - posterior ischemic optic neuropathy", "PION - posterior ischaemic optic neuropathy", "Posterior ischemic optic neuropathy (disorder)", "Posterior ischemic optic neuropathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Posterior Ischemic Optic Neuropathy", "shortest_name_length": 35}
{"curie": "MONDO:0019409", "names": ["Ijo", "IJO", "Juvenile osteoporosis", "juvenile osteoporosis", "osteoporosis, juvenile", "OSTEOPOROSIS, JUVENILE", "Osteoporosis, juvenile", "Pediatric osteoporosis", "Pediatric Osteoporosis", "Idiopathic osteoporosis", "idiopathic osteoporosis", "osteoporosis; idiopathic", "idiopathic; osteoporosis", "Idiopathic juvenile osteoporosis", "idiopathic juvenile osteoporosis", "IDIOPATHIC JUVENILE OSTEOPOROSIS", "Idiopathic Juvenile Osteoporosis", "Idiopathic osteoporosis (disorder)", "idiopathic osteoporosis (diagnosis)", "Idiopathic osteoporosis, site unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic juvenile osteoporosis", "shortest_name_length": 3}
{"curie": "MONDO:0008912", "names": ["cardiac septal defects with coarctation of the aorta", "CARDIAC SEPTAL DEFECTS WITH COARCTATION OF THE AORTA", "Cardiac Septal Defects with Coarctation of the Aorta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiac septal defects with coarctation of the aorta", "shortest_name_length": 52}
{"curie": "UMLS:C1711268", "names": ["Cerebellar Paraganglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebellar Paraganglioma", "shortest_name_length": 24}
{"curie": "MONDO:0011290", "names": ["DISLOCATED ELBOWS, BOWED TIBIAS, SCOLIOSIS, DEAFNESS, CATARACT, MICROCEPHALY, AND MENTAL RETARDATION", "Dislocated Elbows, Bowed Tibias, Scoliosis, Deafness, Cataract, Microcephaly, And Mental Retardation", "dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, and mental retardation", "dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, and intellectual disability", "shortest_name_length": 100}
{"curie": "MONDO:0013483", "names": ["OBHD", "Obesity, Hyperphagia, and Developmental Delay", "OBESITY, HYPERPHAGIA, AND DEVELOPMENTAL DELAY", "obesity, hyperphagia, and developmental delay", "Early-onset obesity-hyperphagia-severe developmental delay syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "obesity, hyperphagia, and developmental delay", "shortest_name_length": 4}
{"curie": "UMLS:C1141930", "names": ["Post procedural complication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post procedural complication", "shortest_name_length": 28}
{"curie": "MONDO:0032670", "names": ["DBA20", "Diamond-Blackfan anemia 20", "DIAMOND-BLACKFAN ANEMIA 20", "RPS15A-related Diamond-Blackfan anemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diamond-Blackfan anemia 20", "shortest_name_length": 5}
{"curie": "UMLS:C5555093", "names": ["Desmoplastic Myxoid Tumor, SMARCB1-Mutant", "Desmoplastic Myxoid Tumor of the Pineal Region, SMARCB1-Mutant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Desmoplastic Myxoid Tumor of the Pineal Region, SMARCB1-Mutant", "shortest_name_length": 41}
{"curie": "MONDO:0008971", "names": ["Chondrodysplasia Calcificans Metaphysealis", "chondrodysplasia calcificans Metaphysealis", "CHONDRODYSPLASIA CALCIFICANS METAPHYSEALIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chondrodysplasia calcificans Metaphysealis", "shortest_name_length": 42}
{"curie": "MONDO:0010464", "names": ["X-linked intellectual disability Kroes type", "X-linked intellectual disability, Kroes type", "X-linked cerebral-cerebellar-coloboma syndrome", "CEREBRAL-CEREBELLAR-COLOBOMA SYNDROME, X-LINKED", "cerebral-cerebellar-coloboma syndrome, X-linked", "X-linked cerebral, cerebellar, coloboma syndrome", "X-linked cerebral-cerebellar-coloboma syndrome syndrome", "X-linked cerebral, cerebellar, coloboma syndrome (disorder)", "X-linked cerebral, cerebellar, coloboma syndrome (diagnosis)", "cerebral-cerebellar-coloboma syndrome, X-linked, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked cerebral-cerebellar-coloboma syndrome syndrome", "shortest_name_length": 43}
{"curie": "UMLS:C0341563", "names": ["anastomotic leak esophagus", "Esophageal anastomotic leak", "Oesophageal anastomotic leak", "Esophageal Anastomotic Leakage", "Esophageal anastomotic leak (disorder)", "Esophageal anastomotic leak (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Anastomotic Leakage", "shortest_name_length": 26}
{"curie": "UMLS:C3658339", "names": ["Chemically-Induced Disorder", "Chemically Induced Disorders", "Chemically-Induced Disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chemically-Induced Disorders", "shortest_name_length": 27}
{"curie": "UMLS:C1336867", "names": ["Anaplastic Urethra Carcinoma", "Anaplastic Urethral Carcinoma", "Anaplastic Carcinoma of Urethra", "anaplastic carcinoma of urethra", "Undifferentiated Urethral Cancer", "Undifferentiated Urethra Carcinoma", "Undifferentiated Urethral Carcinoma", "Urethral Undifferentiated Carcinoma", "Anaplastic Carcinoma of the Urethra", "undifferentiated carcinoma of urethra", "Undifferentiated Carcinoma of Urethra", "Undifferentiated Carcinoma of the Urethra", "anaplastic carcinoma of urethra (diagnosis)", "undifferentiated carcinoma of urethra (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anaplastic carcinoma of urethra", "shortest_name_length": 28}
{"curie": "MONDO:0008522", "names": ["synovial chondromatosis, familial with dwarfism", "SYNOVIAL CHONDROMATOSIS, FAMILIAL, WITH DWARFISM", "synovial chondromatosis, familial, with dwarfism", "Synovial Chondromatosis, Familial, with Dwarfism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "synovial chondromatosis, familial, with dwarfism", "shortest_name_length": 47}
{"curie": "UMLS:C4764202", "names": ["Bladder Non-Invasive Urothelial Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder Non-Invasive Urothelial Neoplasm", "shortest_name_length": 40}
{"curie": "UMLS:C0279615", "names": ["Mixed Alveolar Rhabdomyosarcoma", "mixed pediatric rhabdomyosarcoma", "Pediatric Mixed Rhabdomyosarcoma", "mixed childhood rhabdomyosarcoma", "Mixed Childhood Rhabdomyosarcoma", "childhood rhabdomyosarcoma, mixed", "rhabdomyosarcoma, childhood mixed", "rhabdomyosarcoma, pediatric mixed", "rhabdomyosarcoma, mixed childhood", "pediatric rhabdomyosarcoma, mixed", "Childhood Mixed Type Rhabdomyosarcoma", "mixed type pediatric rhabdomyosarcoma", "mixed type childhood rhabdomyosarcoma", "Pediatric Mixed Type Rhabdomyosarcoma", "Childhood Mixed Alveolar Rhabdomyosarcoma", "Pediatric Mixed Cell Type Rhabdomyosarcoma", "mixed cell type pediatric rhabdomyosarcoma", "mixed cell type childhood rhabdomyosarcoma", "Childhood Mixed Cell Type Rhabdomyosarcoma", "Childhood Rhabdomyosarcoma with Mixed Embryonal and Alveolar Features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Rhabdomyosarcoma with Mixed Embryonal and Alveolar Features", "shortest_name_length": 31}
{"curie": "UMLS:C0544796", "names": ["Proliferative Myositis", "Proliferative myositis", "Myositis, Proliferative", "Proliferative Myositides", "Myositides, Proliferative", "Proliferative myositis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myositis, Proliferative", "shortest_name_length": 22}
{"curie": "MONDO:0016749", "names": ["tumor of cranial and spinal nerves", "rare tumor of cranial and spinal nerves"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tumor of cranial and spinal nerves", "shortest_name_length": 34}
{"curie": "UMLS:C1332500", "names": ["Benign Fibrohistiocytic Tumor", "Benign fibrohistiocytic tumor", "Benign fibrohistiocytic tumour", "Benign fibrohistiocytic neoplasm", "Benign Fibrohistiocytic Neoplasm", "Benign fibrohistiocytic neoplasm (disorder)", "Benign fibrohistiocytic neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign fibrohistiocytic neoplasm", "shortest_name_length": 29}
{"curie": "UMLS:C1335909", "names": ["Salivary Gland Sebaceous Lymphadenoma", "Sebaceous Lymphadenoma of Salivary Gland", "Sebaceous Lymphadenoma of the Salivary Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Salivary Gland Sebaceous Lymphadenoma", "shortest_name_length": 37}
{"curie": "MONDO:0012092", "names": ["HSAN5", "HSAN 5", "HSAN V", "Asymbolia", "asymbolia", "HSAN Type V", "Congenital Analgesia", "congenital analgesia", "Analgesia, Congenital", "Congenital pain asymbolia", "Congenital Pain Indifference", "Pain Indifference, Congenital", "Congenital Pain Insensitivity", "Congenital Pain Indifferences", "congenital insensitivity pain", "congenital pain insensitivity", "PAIN INDIFFERENCE, CONGENITAL", "Insensitivity, Congenital Pain", "Pain Insensitivity, Congenital", "Congenital Indifference to Pain", "Congenital indifference to pain", "Congenital Insensitivity To Pain", "Congenital insensitivity to pain", "Insensitivity To Pain, Congenital", "INSENSITIVITY TO PAIN, CONGENITAL", "insensitivity to pain, congenital", "Congenital indifference to pain (finding)", "Channelopathy-Associated Insensitivity To Pain", "Hereditary Sensory Autonomic Neuropathy, Type 5", "Hereditary sensory and autonomic neuropathy type 5", "Hereditary Sensory and Autonomic Neuropathy Type V", "hereditary sensory and autonomic neuropathy type 5", "hereditary sensory and autonomic neuropathy type V", "Hereditary sensory and autonomic neuropathy type V", "Hereditary sensory and autonomic neuropathy, type V", "Hereditary Sensory and Autonomic Neuropathy, Type 5", "Neuropathy, Hereditary Sensory And Autonomic, Type V", "Neuropathy, Hereditary Sensory and Autonomic, Type V", "NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE V", "neuropathy, hereditary sensory and autonomic, type V", "neuropathy, hereditary sensory and autonomic, type 5", "Congenital insensitivity to pain and thermal analgesia", "congenital insensitivity to pain and thermal analgesia", "NGF autosomal recessive hereditary sensory and autonomic neuropathy", "Congenital sensory neuropathy with selective loss of small myelinated fibres", "Congenital sensory neuropathy with selective loss of small myelinated fibers", "Congenital sensory neuropathy with selective loss of small myelinated fibers (disorder)", "autosomal recessive hereditary sensory and autonomic neuropathy caused by mutation in NGF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary sensory and autonomic neuropathy type 5", "shortest_name_length": 5}
{"curie": "MONDO:0015151", "names": ["autosomal dominant limb-girdle muscular dystrophy", "limb-girdle muscular dystrophy, autosomal dominant", "muscular dystrophy, limb-girdle, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy, limb-girdle, autosomal dominant", "shortest_name_length": 49}
{"curie": "MONDO:0018271", "names": ["PNE", "pnet", "pPNET", "PPNET", "Peripheral PNET", "peripheral PNET", "sarcoma, Ewing's", "Ewing sarcoma/PNET", "Ewing tumor of bone", "Ewing sarcoma / PNET", "Peripheral neuroblastoma", "Peripheral Neuroblastoma", "Ewing's family of tumors", "Peripheral Neuroepithelioma", "peripheral neuroepithelioma", "Peripheral neuroepithelioma", "neuroepithelioma, peripheral", "NEUROEPITHELIOMA, PERIPHERAL", "Neuroepithelioma, Peripheral", "Peripheral Neuroepitheliomas", "Neuroepitheliomas, Peripheral", "peripheral neuroectodermal tumor", "Neuro-Differentiated Ewing Tumor", "Peripheral Neuroectodermal Tumor", "Peripheral neuroectodermal tumor", "Peripheral Neuroectodermal Tumors", "Tumor, Peripheral Neuroectodermal", "Peripheral neuroectodermal tumour", "Neuroectodermal Tumor, Peripheral", "PNE - Peripheral neuroepithelioma", "Neuroectodermal Tumors, Peripheral", "Tumors, Peripheral Neuroectodermal", "Peripheral Neuroectodermal Neoplasm", "peripheral neuroectodermal neoplasm", "Peripheral neuroepithelioma (disorder)", "primitive neuroectodermal tumor (PNET)", "peripheral neuroectodermal tumor (PNET)", "Peripheral neuroepithelioma (diagnosis)", "peripheral primitive neuroectodermal tumor", "Peripheral primitive neuroectodermal tumor", "primitive peripheral neuroectodermal tumor", "Peripheral Primitive Neuroectodermal Tumor", "Peripheral Primitive Neuroectodermal Tumors", "primitive neuroectodermal tumor, peripheral", "Neuroectodermal Tumor, Peripheral Primitive", "Peripheral neuroectodermal tumor (disorder)", "Peripheral primitive neuroectodermal tumour", "peripheral neuroectodermal tumor (diagnosis)", "Extracranial Primitive Neuroectodermal Tumor", "Primitive Neuroectodermal Tumor, Extracranial", "peripheral primitive neuroectodermal neoplasm", "Peripheral primitive neuroectodermal neoplasm", "Peripheral Primitive Neuroectodermal Neoplasm", "Neuroectodermal Tumors, Primitive, Peripheral", "Neuroectodermal Neoplasm, Peripheral Primitive", "Ewing sarcoma / peripheral neuroectodermal tumor", "Ewing sarcoma / peripheral neuroectodermal tumour", "(pPNET) Peripheral Primitive Neuroectodermal Tumors", "Ewing sarcoma/primitive neuroectodermal tumor (PNET)", "Ewing's sarcoma/primitive neuroectodermal tumor (PNET)", "Peripheral neuroectodermal tumor (morphologic abnormality)", "skin neoplasm malignant primary peripheral neuroepithelioma", "malignant neoplasm primary peripheral neuroectodermal tumor", "Ewing sarcoma/peripheral primitive neuroectodermal tumor (PNET)", "Ewing sarcoma / peripheral neuroectodermal tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peripheral primitive neuroectodermal tumor", "shortest_name_length": 3}
{"curie": "MONDO:0013702", "names": ["MRT27", "mental retardation, autosomal recessive 27", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 27", "intellectual disability, autosomal recessive 27", "mental retardation, autosomal recessive type 27", "intellectual disability, autosomal recessive type 27", "autosomal recessive intellectual developmental disorder 27", "intellectual developmental disorder, autosomal recessive 27", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 27", "LINS1 autosomal recessive non-syndromic intellectual disability", "autosomal recessive non-syndromic intellectual disability caused by mutation in LINS1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 27", "shortest_name_length": 5}
{"curie": "MONDO:0019540", "names": ["diffuse alveolar hemorrhage", "diffuse alveolar hemorrhage (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diffuse alveolar hemorrhage", "shortest_name_length": 27}
{"curie": "UMLS:C4553583", "names": ["IIIA", "Stage IIIA Cervical Cancer", "Stage IIIA Cervical Cancer AJCC v8", "Stage IIIA Cervical Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Cervical Cancer AJCC v8", "shortest_name_length": 4}
{"curie": "UMLS:C1336204", "names": ["stage IIIA cervical cancer", "cervical cancer stage IIIA", "Stage IIIA Cervical Cancer", "Cervical Cancer Stage IIIA", "AJCC Stage IIIA Cervical Cancer", "AJCC stage IIIA cervical cancer", "FIGO Stage IIIA Cervix Carcinoma", "FIGO stage IIIA cervix carcinoma", "Stage IIIA Cervical Cancer AJCC v7", "FIGO Stage IIIA Cervical Carcinoma", "stage IIIA cervical cancer AJCC v7", "FIGO stage IIIA cervical carcinoma", "Stage IIIA Cervical Cancer AJCC v6", "stage IIIA cervical cancer AJCC v6", "FIGO stage IIIA carcinoma of cervix", "FIGO Stage IIIA Carcinoma of Cervix", "FIGO Stage IIIA Cervix Uteri Carcinoma", "FIGO stage IIIA cervix uteri carcinoma", "FIGO stage IIIA carcinoma of the cervix", "FIGO Stage IIIA Carcinoma of the Cervix", "FIGO Stage IIIA Uterine Cervix Carcinoma", "FIGO stage IIIA uterine cervix carcinoma", "FIGO stage IIIA carcinoma of cervix uteri", "FIGO Stage IIIA Carcinoma of Cervix Uteri", "Stage IIIA Cervical Cancer AJCC v6 and v7", "FIGO Stage IIIA Carcinoma of Uterine Cervix", "FIGO Stage IIIA carcinoma of uterine cervix", "FIGO stage IIIA carcinoma of the cervix uteri", "FIGO Stage IIIA Carcinoma of the Cervix Uteri", "FIGO stage IIIA carcinoma of the uterine cervix", "FIGO Stage IIIA Carcinoma of the Uterine Cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Cervical Cancer AJCC v6 and v7", "shortest_name_length": 26}
{"curie": "MONDO:0043549", "names": ["Bywaters", "Crush kidney", "crush kidney", "Crush syndrome", "Crush Syndrome", "crush syndrome", "syndrome; crush", "crush; syndrome", "syndrome, crush", "Crush Syndromes", "crush syndromes", "Syndrome, Crush", "Syndromes, Crush", "syndromes, crush", "crushing syndrome", "Bywaters' syndrome", "bywaters' syndrome", "Injury-crush syndrome", "Myoglobinuric nephrosis", "myoglobinuric nephrosis", "Nephrosis, myoglobinuric", "syndrome; crushing injury", "crushing injury; syndrome", "Crush syndrome (disorder)", "crush syndrome (diagnosis)", "kidney injury crush syndrome", "Renal failure following crushing", "Myoglobinuric acute renal failure", "myoglobinuric acute renal failure", "ischemic muscular necrosis syndrome", "Ischemic muscular necrosis syndrome", "Ischaemic muscular necrosis syndrome", "renal failure following crushing injury", "Renal failure following crushing injury", "acute renal failure due to rhabdomyolysis", "Acute renal failure due to rhabdomyolysis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "crush syndrome", "shortest_name_length": 8}
{"curie": "UMLS:C0403527", "names": ["scleroderma acute renal crisis", "Acute scleroderma renal crisis", "Acute scleroderma renal crisis (disorder)", "Acute scleroderma renal crisis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute scleroderma renal crisis", "shortest_name_length": 30}
{"curie": "UMLS:C0679407", "names": ["Gastrointestinal Dysfunction", "Gastrointestinal dysfunction", "gastrointestinal dysfunction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal dysfunction", "shortest_name_length": 28}
{"curie": "MONDO:0018193", "names": ["testis; teratoma", "teratoma; testis", "TESTIS, TERATOMA", "Teratoma of testis", "teratoma of testes", "teratoma of testis", "Teratoma of Testis", "Teratoma of testes", "Testicular teratoma", "testicular teratoma", "TESTICULAR TERATOMA", "Testicular Teratoma", "TERATOMA, TESTICULAR", "Teratoma, Testicular", "teratomas testicular", "teratoma, testicular", "Teratoma of the testis", "Teratoma of the Testis", "teratoma of the testis", "testis cancer, teratoma", "testicle cancer, teratoma", "teratoma testicular cancer", "testicular cancer, teratoma", "Teratoma of testis (disorder)", "testicular teratoma (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular teratoma", "shortest_name_length": 16}
{"curie": "UMLS:C3887486", "names": ["Interstitial fibrosis", "interstitial fibrosis", "fibrosis interstitial", "FIBROSIS, INTERSTITIAL", "interstitial lung fibrosis", "Interstitial lung fibrosis", "Lung fibrosis interstitial", "LUNG FIBROSIS INTERSTITIAL", "fibrosis interstitial lungs", "PULMONARY FIBROSIS INTERSTITIAL", "fibrosis interstitial pulmonary", "INTERSTITIAL PULMONARY FIBROSIS", "interstitial pulmonary fibrosis", "pulmonary interstitial fibrosis", "Interstitial pulmonary fibrosis", "pulmonary fibrosis interstitial", "Fibrosing interstitial pneumonitis", "Interstitial fibrosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Interstitial lung fibrosis", "shortest_name_length": 21}
{"curie": "MONDO:0020432", "names": ["ectasia of the right atrial auricle", "ectasia of the right atrial appendage", "dilatation of the right atrial auricle", "dilatation of the right atrial appendage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectasia of the right atrial appendage", "shortest_name_length": 35}
{"curie": "MONDO:0000476", "names": ["Dystonia 12", "dystonia 12", "torsion dystonia", "familial dystonia", "dystonias, torsion", "Generalized dystonia", "Generalised dystonia", "generalized dystonia", "Dystonia, generalized", "Oppenheim Ziehen disease", "Oppenheim-Ziehen disease", "Progressive torsion spasm", "childhood torsion disease", "spasm, Progressive torsion", "torsion spasm, Progressive", "torsion disease, childhood", "Idiopathic torsion dystonia", "idiopathic torsion dystonia", "torsion disease of childhood", "idiopathic familial dystonia", "symptomatic torsion dystonia", "Idiopathic torsion dystonias", "dystonia, Idiopathic torsion", "Symptomatic torsion dystonia", "torsion dystonia, Idiopathic", "fragments of torsion dystonia", "dystonia deformans musculorum", "Fragments of torsion dystonia", "generalized isolated dystonia", "dystonia musculorum deformans", "Dystonia Musculorum Deformans", "dystonias, Idiopathic torsion", "dystonia; torsion, symptomatic", "dystonia deformans progressiva", "Generalized dystonia (disorder)", "idiopathic non-familial dystonia", "Fragment of torsion dystonia, NOS", "Symptomatic torsion dystonia (disorder)", "Fragments of torsion dystonia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "generalized dystonia", "shortest_name_length": 11}
{"curie": "MONDO:0800140", "names": ["ITPKB deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ITPKB deficiency", "shortest_name_length": 16}
{"curie": "MONDO:0009126", "names": ["atresia duodenal", "Duodenal Atresia", "Duodenal atresia", "duodenal atresia", "Duodenum atresia", "DUODENAL ATRESIA", "atresia; duodenum", "DUODENUM, ATRESIA", "duodenum; atresia", "duodenal stenosis", "Atresia of duodenum", "atresia of duodenum", "Atresia of Duodenum", "Familial duodenal atresia", "duodenal atresia (disease)", "Duodenal atresia congenital", "Congenital duodenal atresia", "Congenital Duodenal Atresia", "DUODENAL ATRESIA CONGENITAL", "congenital duodenal atresia", "Congenital atresia of duodenum", "congenital atresia of duodenum", "Congenital Atresia of Duodenum", "atresia of duodenum (diagnosis)", "Congenital atresia of duodenum (disorder)", "Absence or narrowing of first part of small bowel"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "duodenal atresia", "shortest_name_length": 16}
{"curie": "MONDO:0013735", "names": ["MCHCCD", "ZAKI-GLEESON SYNDROME", "Zaki-Gleeson syndrome", "Zaki Gleeson syndrome", "microcephaly-cerebellar hypoplasia-cardiac conduction defect syndrome", "Microcephaly-cerebellar hypoplasia-cardiac conduction defect syndrome", "Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome", "microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome", "MICROCEPHALY, CEREBELLAR HYPOPLASIA, AND CARDIAC CONDUCTION DEFECT SYNDROME", "microcephaly, cerebellar hypoplasia, and CARDIAC conduction defect syndrome", "Microcephaly-cerebellar hypoplasia-congenital heart conduction defect syndrome", "microcephaly-cerebellar hypoplasia-congenital heart conduction defect syndrome", "Microcephaly, cerebellar hypoplasia, congenital heart conduction defect syndrome", "Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome (disorder)", "microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly-cerebellar hypoplasia-cardiac conduction defect syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0800131", "names": ["HIES4A", "HYPER-IgE RECURRENT INFECTION SYNDROME 4A, AUTOSOMAL DOMINANT", "hyper-IgE recurrent infection syndrome 4A, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyper-IgE recurrent infection syndrome 4A, autosomal dominant", "shortest_name_length": 6}
{"curie": "MONDO:0018229", "names": ["Stevens-Johnson", "johnson steven syndrome", "steven johnson syndrome", "steven jonhson syndrome", "STEVEN JOHNSON SYNDROME", "STEVENS JOHNSON SYNDROME", "johnson reaction stevens", "Stevens-Johnson Syndrome", "steven johnsons syndrome", "stevens johnson reaction", "Stevens-Johnson syndrome", "Stevens Johnson reaction", "johnson stevens syndrome", "SYNDROME STEVENS-JOHNSON", "stevens-johnson syndrome", "johnsons steven syndrome", "STEVENS-JOHNSON SYNDROME", "Stevens Johnson syndrome", "stevens johnson syndrome", "Stevens Johnson Syndrome", "Syndrome Stevens-Johnson", "johnsons stevens syndrome", "erythema multiforme major", "Erythema multiforme major", "stevens johnsons syndrome", "Erythema Multiforme Major", "Bullous erythema multiforme", "bullous erythema multiforme", "Erythema multiforme bullosum", "Erythema Multiforme Bullosum", "erythema; multiforme bullosum", "Erythema exudativum multiforme", "erythema multiforme exudativum", "FEBRILE MUCOCUTANEOUS SYNDROME", "Erythema multiforme exudativum", "ERYTHEMA MULTIFORME EXUDATIVUM", "Erythema exsudativum multiforme", "erythema exsudativum multiforme", "Stevens-Johnson syndrome (disorder)", "Stevens-Johnson syndrome (EM major)", "Stevens-Johnson syndrome (diagnosis)", "Ectodermosis erosiva pluriorificialis", "SYNOVITIS, CHRONIC, SUSCEPTIBILITY TO", "ectodermosis erosiva pluriorificialis", "Dermatostomatitis, Stevens Johnson type", "Erythema multiforme, Stevens-Johnson type", "STEVENS-JOHNSON SYNDROME, SUSCEPTIBILITY TO", "Stevens-Johnson syndrome, susceptibility to", "ABACAVIR HYPERSENSITIVITY, SUSCEPTIBILITY TO", "ANKYLOSING SPONDYLITIS, SUSCEPTIBILITY TO, 1", "TOXIC EPIDERMAL NECROLYSIS, SUSCEPTIBILITY TO", "toxic Epidermal necrolysis, susceptibility to", "DRUG-INDUCED LIVER INJURY DUE TO FLUCLOXACILLIN", "severe cutaneous adverse reaction, susceptibility to", "SEVERE CUTANEOUS ADVERSE REACTION, SUSCEPTIBILITY TO", "Erythema Multiforme Bullosum (Stevens Johnson Syndrome)", "HYPERSENSITIVITY SYNDROME, CARBAMAZEPINE-INDUCED, SUSCEPTIBILITY TO", "hypersensitivity syndrome, carbamazepine-induced, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stevens-Johnson syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0005255", "names": ["mild heart failure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mild heart failure", "shortest_name_length": 18}
{"curie": "MONDO:0002382", "names": ["Benign Mesenchymoma", "benign mesenchymoma", "Benign mesenchymoma", "Mesenchymoma, benign", "mesenchymoma, benign", "mesenchymal tumor, benign", "MESENCHYMAL TUMOR, BENIGN", "Mesenchymoma, benign (morphologic abnormality)", "mesenchymoma, benign (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign mesenchymoma", "shortest_name_length": 19}
{"curie": "MONDO:0008299", "names": ["BIEMOND ATAXIA", "Biemond ataxia", "posterior column ataxia", "POSTERIOR COLUMN ATAXIA", "Posterior column ataxia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "posterior column ataxia", "shortest_name_length": 14}
{"curie": "MONDO:0011647", "names": ["Ad7", "AD7", "Alzheimer disease-7", "Alzheimer disease 7", "Alzheimer Disease 7", "ALZHEIMER DISEASE 7", "Alzheimer's disease 7", "Alzheimer disease type 7", "Alzheimer's disease type 7", "Alzheimer disease, familial 7", "Alzheimer Disease, Familial, 7", "Alzheimer disease, familial, 7", "ALZHEIMER DISEASE, FAMILIAL, 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alzheimer disease 7", "shortest_name_length": 3}
{"curie": "MONDO:0042912", "names": ["Schlegelberger-Grote syndrome", "Schlegelberger Grote syndrome", "Triphalangeal thumbs thrombocytopathy deafness", "triphalangeal thumbs thrombocytopathy deafness", "Syndrome with triphalangia of thumbs, thrombasthenia Glanzmann and deafness of internal ear", "syndrome with triphalangia of thumbs, thrombasthenia Glanzmann and deafness of internal ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Schlegelberger-Grote syndrome", "shortest_name_length": 29}
{"curie": "UMLS:C1334219", "names": ["Intermediate Risk Colorectal Gastrointestinal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intermediate Risk Colorectal Gastrointestinal Stromal Tumor", "shortest_name_length": 59}
{"curie": "MONDO:0000450", "names": ["SPMS", "secondary-progressive MS", "Secondary-progressive MS", "secondary progressive multiple sclerosis", "multiple sclerosis progressive secondary", "Secondary progressive multiple sclerosis", "Secondary Progressive Multiple Sclerosis", "Multiple Sclerosis, Secondary Progressive", "Multiple sclerosis (MS) secondary progressive", "Secondary progressive multiple sclerosis (disorder)", "Secondary progressive multiple sclerosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary progressive multiple sclerosis", "shortest_name_length": 4}
{"curie": "UMLS:C3640036", "names": ["Thoracic Meningocele"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thoracic Meningocele", "shortest_name_length": 20}
{"curie": "MONDO:0018445", "names": ["GLOW", "GLOW syndrome", "glow syndrome", "GLOW SYNDROME", "GLOW syndrome, somatic mosaic", "global developmental delay, lung cysts, overgrowth, and wilms tumor", "GLOBAL DEVELOPMENTAL DELAY, LUNG CYSTS, OVERGROWTH, AND WILMS TUMOR", "Global developmental delay-lung cysts-overgrowth-Wilms tumor syndrome", "Global developmental delay, lung cysts, overgrowth, Wilms tumor syndrome", "Global developmental delay, lung cysts, overgrowth, Wilms tumour syndrome", "global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome", "GLOW (global developmental delay, lung cysts, overgrowth, Wilms tumor) syndrome", "GLOW (global developmental delay, lung cysts, overgrowth, Wilms tumour) syndrome", "Global developmental delay, lung cysts, overgrowth, Wilms tumor syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0005464", "names": ["Retinal detachment with break", "Retinal detachments and breaks", "Rhegmatogenous retinal detachment", "Rhegmatogenous Retinal Detachment", "retinal detachment rhegmatogenous", "rhegmatogenous retinal detachment", "detachment retinal rhegmatogenous", "retina; detachment, rhegmatogenous", "detachments retinal rhegmatogenous", "detachment; retina, rhegmatogenous", "rhegmatogenous detachment of retina", "Retinal detachment with retinal break", "Rhegmatogenous retinal detachment (disorder)", "rhegmatogenous retinal detachment (diagnosis)", "Retinal detachment due to full thickness retinal tear", "rhegmatogenous detachment of retina (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rhegmatogenous retinal detachment", "shortest_name_length": 29}
{"curie": "MONDO:0003962", "names": ["Fröhlich", "Fröhlich syndrome", "Fröhlich Syndrome", "Adiposodysgenesis", "Frohlich syndrome", "frohlich syndrome", "Frohlich Syndrome", "Froelich syndrome", "sexual infantilism", "Frolich's Syndrome", "frohlichs syndrome", "FROEHLICH SYNDROME", "froehlich syndrome", "Frolich's syndrome", "Froehlich syndrome", "Sexual Infantilism", "Froehlich Syndrome", "Frohlich's Syndrome", "Froehlichs Syndrome", "Froelich's Syndrome", "Frohlich's syndrome", "frohlich's syndrome", "Froelich's syndrome", "Froehlich's Syndrome", "Froelich's adiposity", "Froehlich's syndrome", "Syndrome, Froehlich's", "adiposogenital syndrome", "Launois-Cleret Syndrome", "Adiposogenital syndrome", "Launois-Cleret syndrome", "syndrome; adiposogenital", "adiposogenital dystrophy", "Adiposogenital dystrophy", "adiposogenital; syndrome", "ADIPOSOGENITAL DYSTROPHY", "Adiposogenital Dystrophy", "adiposogenital; dystrophy", "dystrophy; adiposogenital", "Babinski-Froelich Syndrome", "Babinski-Froelich syndrome", "dystrophia Adiposogenitalis", "Dystrophia Adiposogenitalis", "Hypothalamic Infantilism-Obesity", "hypothalamic infantilism-obesity", "Froehlich's syndrome (diagnosis)", "Adiposogenital dystrophy syndrome", "Adiposogenital dystrophy (disorder)", "Hypothalamic infantilism with obesity syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Froelich syndrome", "shortest_name_length": 8}
{"curie": "UMLS:C0342386", "names": ["FSH Deficiency", "Follicle Stimulating Hormone Deficiency", "Follicle stimulating hormone deficiency", "FSH - follicle stimulating hormone deficiency", "Follicle stimulating hormone deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Follicle stimulating hormone deficiency", "shortest_name_length": 14}
{"curie": "MONDO:0007662", "names": ["IHGA", "IGDS", "ASGD4", "IRID2", "PITX2 iridogoniodysgenesis", "iridogoniodysgenesis type 2", "Iridogoniodysgenesis type 2", "Iridogoniodysgenesis, Type 2", "iridogoniodysgenesis, type 2", "IRIDOGONIODYSGENESIS, TYPE 2", "Iridogoniodysgenesis syndrome", "iridogoniodysgenesis syndrome", "IRIDOGONIODYSGENESIS SYNDROME", "ANTERIOR SEGMENT DYSGENESIS 4", "anterior segment dysgenesis 4", "Iridogoniodysgenesis, dominant type", "iridogoniodysgenesis caused by mutation in PITX2", "Iris hypoplasia with early onset glaucoma, autosomal dominant", "iris hypoplasia with early-onset glaucoma, autosomal dominant", "Iris Hypoplasia With Early-Onset Glaucoma, Autosomal Dominant", "IRIS HYPOPLASIA WITH EARLY-ONSET GLAUCOMA, AUTOSOMAL DOMINANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anterior segment dysgenesis 4", "shortest_name_length": 4}
{"curie": "UMLS:C3272607", "names": ["Colorectal NEC", "Colorectal NEC G3", "Colorectal Neuroendocrine Carcinoma", "Large Intestinal Neuroendocrine Carcinoma", "Colorectal (Colon or Rectal) Neuroendocrine Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Neuroendocrine Carcinoma", "shortest_name_length": 14}
{"curie": "UMLS:C5419564", "names": ["Refractory Myeloid Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Myeloid Neoplasm", "shortest_name_length": 27}
{"curie": "UMLS:C2936406", "names": ["Dystroglycanopathy", "Alpha-dystroglycanopathy", "alpha Dystroglycanopathies", "alpha-Dystroglycanopathies", "Qualitative or quantitative defects of alpha-dystroglycan"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alpha-Dystroglycanopathies", "shortest_name_length": 18}
{"curie": "MONDO:0005803", "names": ["nesidioblastosis", "islet cell hyperplasia", "Islet cell hyperplasia", "hyperinsulinemic hypoglycemia", "hyperinsulinemia hypoglycemia", "hyperinsulinemic hypoglycemia (disease)", "persistent hyperinsulinemia hypoglycemia of infancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperinsulinemic hypoglycemia", "shortest_name_length": 16}
{"curie": "UMLS:C2348377", "names": ["Ectopic ventricular rhythm", "ECTOPIC VENTRICULAR RHYTHM", "Ectopic Ventricular Rhythm", "Ectopic Ventricular Rhythm by ECG Finding", "Ectopic Ventricular Rhythm by EKG Finding"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ectopic Ventricular Rhythm by ECG Finding", "shortest_name_length": 26}
{"curie": "UMLS:C0149676", "names": ["Enzyme Deficiency", "Deficiency;enzyme", "ENZYME DEFICIENCY", "deficiency enzyme", "enzyme deficiency", "deficiency enzymes", "enzymes; deficiency", "deficiencies enzyme", "deficiency; enzymes", "deficiencies enzymes", "Specific enzyme deficiency", "Specific Enzyme Deficiency", "Specific enzyme deficiency (disorder)", "Specific enzyme deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Enzyme Deficiency", "shortest_name_length": 17}
{"curie": "UMLS:C0280149", "names": ["Stage II Diffuse Large Cell Lymphoma", "Stage II Adult Diffuse Large Cell Lymphoma", "stage II adult diffuse large cell lymphoma", "Adult Diffuse Large Cell Lymphoma Stage II", "adult diffuse large cell lymphoma, stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Adult Diffuse Large Cell Lymphoma", "shortest_name_length": 36}
{"curie": "MONDO:0043904", "names": ["cheloid leishmaniasis", "Leproid leishmaniasis", "Cheloid leishmaniasis", "leproid leishmaniasis", "Diffuse Cutaneous Leishmaniases", "diffuse cutaneous Leishmaniases", "diffuse cutaneous leishmaniasis", "Diffuse cutaneous leishmaniasis", "Diffuse Cutaneous Leishmaniasis", "leishmaniasis cutaneous diffuse", "Cutaneous Leishmaniases, Diffuse", "Leishmaniases, diffuse cutaneous", "Leishmaniases, Diffuse Cutaneous", "Leishmaniasis, Diffuse Cutaneous", "cutaneous leishmaniasis, diffuse", "Cutaneous leishmaniasis, diffuse", "Cutaneous Leishmaniasis, Diffuse", "cutaneous Leishmaniases, diffuse", "leishmaniasis, diffuse cutaneous", "Leishmania; infection, aethiopica", "infection; Leishmania, aethiopica", "Ethiopian cutaneous leishmaniasis", "Infection by Leishmania ethiopica", "Cutaneous leishmaniasis, Ethiopian", "Cutaneous, ethiopian leishmaniasis", "Infection by Leishmania aethiopica", "Lepromatous cutaneous leishmaniasis", "Leishmaniasis, cutaneous, Ethiopian", "lepromatous cutaneous leishmaniasis", "Cutaneous leishmaniasis, lepromatous", "dcl - diffuse cutaneous leishmaniasis", "DCL - Diffuse cutaneous leishmaniasis", "Diffuse Old World cutaneous leishmaniasis", "diffuse Ethiopian cutaneous leishmaniasis", "Infection caused by Leishmania aethiopica", "Diffuse cutaneous leishmaniasis (disorder)", "Diffuse cutaneous leishmaniasis (diagnosis)", "Ethiopian cutaneous leishmaniasis (diagnosis)", "lepromatous Ethiopian cutaneous leishmaniasis", "Infection caused by Leishmania aethiopica (disorder)", "diffuse Ethiopian cutaneous leishmaniasis (diagnosis)", "lepromatous Ethiopian cutaneous leishmaniasis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leishmaniasis, diffuse cutaneous", "shortest_name_length": 21}
{"curie": "UMLS:C4527255", "names": ["Refractory Pancreatic Neuroendocrine Cancer", "Refractory Pancreatic Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Pancreatic Neuroendocrine Carcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0032642", "names": ["ACCIID", "Craniosynostosis-microretrognathia-severe intellectual disability syndrome", "ARTHROGRYPOSIS, CLEFT PALATE, CRANIOSYNOSTOSIS, AND IMPAIRED INTELLECTUAL DEVELOPMENT", "arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development", "shortest_name_length": 6}
{"curie": "UMLS:C3899125", "names": ["Fetal Chorionic Vasculitis", "Acute Chorionic Vasculitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fetal Chorionic Vasculitis", "shortest_name_length": 26}
{"curie": "UMLS:C5556498", "names": ["High-Grade Bladder Urothelial Carcinoma", "High Grade Bladder Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Bladder Urothelial Carcinoma", "shortest_name_length": 39}
{"curie": "MONDO:0020145", "names": ["developmental defect of the eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental defect of the eye", "shortest_name_length": 31}
{"curie": "MONDO:0003538", "names": ["Precursor Lymphoid Neoplasm", "precursor lymphoid neoplasm", "precursor lymphoblastic leukemia/lymphoma", "Precursor Lymphoblastic Leukemia/Lymphoma", "Precursor Lymphoblastic Lymphoma/Leukemia", "precursor lymphoblastic lymphoma/leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "precursor lymphoblastic lymphoma/leukemia", "shortest_name_length": 27}
{"curie": "UMLS:C0036347", "names": ["Hebephrenia", "hebephrenia", "HEBEPHRENIA", "hebephrenic schizophrenia", "Hebephrenic Schizophrenia", "Hebephrenic schizophrenia", "hebrephrenic schizophrenia", "Schizophrenia, Hebephrenic", "Disorganised schizophrenia", "hebephrenic; schizophrenic", "disorganized schizophrenia", "Hebephrenic Schizophrenias", "Disorganized Schizophrenia", "schizophrenia disorganized", "schizophrenia; hebephrenic", "Disorganized schizophrenia", "disorganized; schizophrenic", "schizophrenia; disorganized", "Schizophrenia, Disorganized", "Schizophrenias, Hebephrenic", "Disorganized Schizophrenias", "Schizophrenias, Disorganized", "Hebephrenic type schizophrenia", "Disorganized Type Schizophrenia", "Disorganized type schizophrenia", "Schizophrenia, hebephrenic type", "Disorganized schizophrenia, NOS", "disorganized schizophrenia type", "Schizophrenia, disorganised type", "Schizophrenia, disorganized type", "Schizophrenia (Disorganized Type)", "Disorganized schizophrenia (disorder)", "disorganized schizophrenia (diagnosis)", "disorganized type schizophrenic disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Schizophrenia, Disorganized", "shortest_name_length": 11}
{"curie": "UMLS:C4688341", "names": ["Recurrent Grade 2 Glioma", "Recurrent Grade II Glioma", "Recurrent WHO Grade 2 Glioma", "Recurrent WHO Grade II Glioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent WHO Grade 2 Glioma", "shortest_name_length": 24}
{"curie": "MONDO:0002940", "names": ["Anal Margin Basal Cell Carcinoma", "Anal margin basal cell carcinoma", "anal margin basal cell carcinoma", "perianal skin basal cell carcinoma", "Perianal Skin Basal Cell Carcinoma", "basal cell carcinoma of anal margin", "Basal Cell Carcinoma of Anal Margin", "Basal cell carcinoma of anal margin", "basal cell carcinoma of perianal skin", "Basal cell carcinoma of perianal skin", "Basal cell carcinoma of Perianal skin", "Basal Cell Carcinoma of Perianal Skin", "perianal skin skin basal cell carcinoma", "basal cell carcinoma of the anal margin", "Basal Cell Carcinoma of the Anal Margin", "basal cell carcinoma of the perianal skin", "Basal Cell Carcinoma of the Perianal Skin", "skin basal cell carcinoma of perianal skin", "basal cell carcinoma of anal margin (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anal margin basal cell carcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C0018775", "names": ["hearing loss bilateral", "Bilateral hearing loss", "Hearing loss bilateral", "Bilateral Hearing Loss", "HEARING LOSS BILATERAL", "bilateral hearing loss", "Hearing loss, bilateral", "Hearing Loss, Bilateral", "Loss, Bilateral Hearing", "Bilateral Hearing Losses", "hearing loss bilaterally", "hearing loss in both ears", "loss of hearing on both sides", "Bilateral hearing loss (disorder)", "hearing loss in both ears (diagnosis)", "loss of hearing on both sides (symptom)", "bilateral hearing loss (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hearing Loss, Bilateral", "shortest_name_length": 22}
{"curie": "MONDO:0043164", "names": ["Palmer Pagon syndrome", "palmer pagon syndrome", "Palmer-Pagon syndrome", "hydrocephaly - low insertion umbilicus", "Hydrocephaly-low insertion umbilicus syndrome", "familial hydrocephalus with a low-insertion umbilicus", "Congenital hydrocephalus, low insertion of umbilicus syndrome", "Congenital hydrocephalus, low insertion of umbilicus syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "palmer pagon syndrome", "shortest_name_length": 21}
{"curie": "UMLS:C3899646", "names": ["Pilomyxoid Astrocytoma", "childhood pilomyxoid astrocytoma", "Childhood Pilomyxoid Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Pilomyxoid Astrocytoma", "shortest_name_length": 22}
{"curie": "UMLS:C0855179", "names": ["Stage IV Bladder Adenocarcinoma", "Bladder adenocarcinoma stage IV", "Stage IV Bladder Adenocarcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder adenocarcinoma stage IV", "shortest_name_length": 31}
{"curie": "UMLS:C5420752", "names": ["Conjunctival Oncocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conjunctival Oncocytoma", "shortest_name_length": 23}
{"curie": "MONDO:0014910", "names": ["CILD35", "primary ciliary dyskinesia 35", "ciliary dyskinesia, primary, 35", "CILIARY DYSKINESIA, PRIMARY, 35", "TTC25 primary ciliary dyskinesia", "primary ciliary dyskinesia type 35", "ciliary dyskinesia, primary, type 35", "primary ciliary dyskinesia caused by mutation in TTC25", "primary ciliary dyskinesia 35 with or without situs inversus", "CILIARY DYSKINESIA, PRIMARY, 35, WITH OR WITHOUT SITUS INVERSUS", "ciliary dyskinesia, primary, 35, with or without situs inversus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia 35", "shortest_name_length": 6}
{"curie": "MONDO:0019262", "names": ["JNCL", "juvenile NCL", "batten disease", "Spielmeyer-Vogt disease", "juvenile neuronal ceroid lipofuscinosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile neuronal ceroid lipofuscinosis", "shortest_name_length": 4}
{"curie": "UMLS:C1696942", "names": ["Application site cellulitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Application site cellulitis", "shortest_name_length": 27}
{"curie": "MONDO:0004671", "names": ["Queyrat Erythroplasia", "erythroplasia queyrat", "Queyrat erythroplasia", "Bowen disease of penis", "ERYTHROPLASIA, QUEYRAT", "Queyrat's erythroplasia", "penis carcinoma in situ", "Cancer in situ of penis", "stage 0 penis carcinoma", "Penis carcinoma in situ", "Queyrat's Erythroplasia", "penis in situ carcinoma", "Bowen's disease of penis", "penile carcinoma in situ", "Bowen's Disease of Penis", "Erythroplasia of Queyrat", "Penile Carcinoma In Situ", "erythroplasia of Queyrat", "erythroplasia of queyrat", "Bowen disease of the penis", "Bowen Disease of the Penis", "carcinoma in situ of penis", "Carcinoma in situ of penis", "Carcinoma in situ of Penis", "Erythroplasia of Queyrat NOS", "Bowen's Disease of the Penis", "Bowen's disease of the penis", "carcinoma in situ of the penis", "Bowen's disease of glans penis", "Carcinoma in situ of the Penis", "Carcinoma in situ of penis, NOS", "Penile Carcinoma In Situ AJCC v7", "CIS - Carcinoma in situ of penis", "penile carcinoma in situ aJCC v7", "stage 0 penile carcinoma in situ", "Queyrat's erythroplasia (disorder)", "Bowen's disease of penis (disorder)", "Bowen's disease of penis (diagnosis)", "Queyrat erythroplasia of glans penis", "Carcinoma in situ of penis (disorder)", "carcinoma in situ of penis (diagnosis)", "penile intraepithelial neoplasia grade III", "Penile intraepithelial neoplasia grade III", "grade III penile intraepithelial neoplasia", "Grade III Penile Intraepithelial Neoplasia", "Queyrat erythroplasia of glans penis (diagnosis)", "Queyrat's erythroplasia (morphologic abnormality)", "grade III squamous intraepithelial lesion of penis", "grade III squamous Intraepithelial Lesion of penis", "Grade III Squamous Intraepithelial Lesion of Penis", "Penile intraepithelial neoplasia grade III (disorder)", "Grade III Squamous Intraepithelial Lesion of the Penis", "grade III squamous intraepithelial lesion of the penis", "Penile intraepithelial neoplasia grade III (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "penis carcinoma in situ", "shortest_name_length": 21}
{"curie": "MONDO:0018467", "names": ["CTNS", "cystinosin, defect of", "nephropathic infantile cystinosis", "cystinosis, atypical nephropathic", "cystinosis, infantile nephropathic", "lysosomal cystine transport protein, defect of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephropathic infantile cystinosis", "shortest_name_length": 4}
{"curie": "MONDO:0012013", "names": ["WMS2", "GEMSS", "GEMSS syndrome", "WEILL-MARCHESANI SYNDROME 2", "Weill-Marchesani syndrome 2", "Weill-Marchesani syndrome type 2", "SPHEROPHAKIA-BRACHYMORPHIA SYNDROME", "spherophakia-brachymorphia syndrome", "Weill-Marchesani syndrome 2, dominant", "MESODERMAL DYSMORPHODYSTROPHY, CONGENITAL", "mesodermal Dysmorphodystrophy, congenital", "Weill-Marchesani Syndrome, Autosomal Dominant", "Weill-Marchesani syndrome, autosomal dominant", "WEILL-MARCHESANI SYNDROME, AUTOSOMAL DOMINANT", "Weill Marchesani Syndrome, Autosomal Dominant", "glaucoma-lens ectopia-microspherophakia-stiffness-shortness syndrome", "Glaucoma-Lens Ectopia-Microspherophakia-Stiffness-Shortness Syndrome", "GLAUCOMA-LENS ECTOPIA-MICROSPHEROPHAKIA-STIFFNESS-SHORTNESS SYNDROME", "Glaucoma, ectopia, microspherophakia, stiff joint, short stature syndrome", "Glaucoma, Ectopia, Microspherophakia, Stiff joints, Short stature syndrome", "glaucoma, ectopia, microspherophakia, Stiff joints and short stature syndrome", "Glaucoma-ectopia lentis-microspherophakia-stiff joints-short stature syndrome", "GEMSS (glaucoma, ectopia, microspherophakia, stiff joint, short stature) syndrome", "Glaucoma, ectopia, microspherophakia, stiff joint, short stature syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Weill-Marchesani syndrome 2, dominant", "shortest_name_length": 4}
{"curie": "UMLS:C0340865", "names": ["anaphylactoid shock", "Anaphylactoid shock", "ANAPHYLACTOID REACTION", "anaphylactoid reaction", "Anaphylactoid reaction", "Anaphylactoid Reaction", "anaphylactoid reactions", "Non-allergic anaphylaxis", "Anaphylactoid reaction NOS", "Anaphylactic type reaction", "SHOCK ANAPHYLACTIC ANAPHYLACTOID", "REACTION ANAPHYLACTIC ANAPHYLACTOID", "Non-allergic anaphylaxis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anaphylactoid Reaction", "shortest_name_length": 19}
{"curie": "UMLS:C0747637", "names": ["Large Pleural Effusion", "PLEURAL EFFUSION LARGE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Large Pleural Effusion", "shortest_name_length": 22}
{"curie": "MONDO:0007871", "names": ["LCDD", "Punctal atresia", "lacrimal duct defect", "LACRIMAL DUCT DEFECT", "Lacrimal duct defects", "Absent lacrimal puncta", "Absent lacrimal punctum", "Lacrimal puncta aplasia", "Absent lacrimal openings", "punctum lacrimale; absent", "Agenesis;lacrimal punctum", "lacrimal punctum agenesis", "Lacrimal punctum, absence", "Lacrimal punctum agenesis", "absence; punctum lacrimale", "Aplasia of lacrimal puncta", "Atresia of lacrimal puncta", "punctum lacrimale; agenesis", "lacrimal puncta, absence of", "LACRIMAL PUNCTA, ABSENCE OF", "agenesis; punctum lacrimale", "Atresia of lacrimal punctum", "Lacrimal Puncta, Absence of", "Agenesis of lacrimal punctum", "Absent lacrimal gland puncta", "Imperforate lacrimal punctum", "Imperforate punctum lacrimale", "nasolacrimal duct obstruction", "Agenesis of punctum lacrimale", "Agenesis of the lacrimal punctum", "Congenital absence of punctum lacrimale", "Imperforate lacrimal punctum (disorder)", "Agenesis of punctum lacrimale (disorder)", "Absence or agenesis of punctum lacrimale", "familial congenital nasolacrimal duct obstruction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial congenital nasolacrimal duct obstruction", "shortest_name_length": 4}
{"curie": "MONDO:0023267", "names": ["goldstein hutt syndrome", "Goldstein Hutt syndrome", "trichomegaly, cataract, and hereditary spherocytosis", "Trichomegaly, cataract, and hereditary spherocytosis", "long eyelashes, cataract, and hereditary spherocytosis", "Long eyelashes, cataract, and hereditary spherocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "goldstein hutt syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0035321", "names": ["Mild aldosterone synthase deficiency", "late-onset familial hypoaldosteronism", "Late-onset familial hyperreninemic hypoaldosteronism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "late-onset familial hypoaldosteronism", "shortest_name_length": 36}
{"curie": "MONDO:0008101", "names": ["POLYMASTIA", "polymastia", "Polymastia", "polythelia", "Polythelia", "Hyperthelia", "hyperthelia", "nipple extra", "extra nipple", "Extra nipple", "extra nipples", "extra; nipple", "Ectopic nipple", "accessory nipple", "Accessory nipple", "ACCESSORY NIPPLE", "nipple accessory", "accessory; nipple", "ACCESSORY NIPPLES", "Accessory Nipples", "accessory nipples", "Accessory nipples", "nipple; accessory", "accessory mamilla", "accessory mamillas", "isolated polythelia", "supernumerary nipple", "Polythelia, Familial", "POLYTHELIA, FAMILIAL", "Nipple supernumerary", "polythelia, familial", "Supernumerary nipple", "Supernumerary nipples", "nipple; supernumerary", "nipples supernumerary", "NIPPLES, SUPERNUMERARY", "Nipples, Supernumerary", "nipples, supernumerary", "Increased nipple number", "Accessory nipple (disorder)", "Congenital accessory nipple", "accessory nipple (diagnosis)", "polythelia (physical finding)", "familial supernumerary nipples", "Supernumerary nipples (polythelia)", "breast appearance nipple polythelia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial supernumerary nipples", "shortest_name_length": 10}
{"curie": "UMLS:C2347922", "names": ["Refractory Adult Spinal Cord Tumor", "Refractory Adult Spinal Cord Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Adult Spinal Cord Neoplasm", "shortest_name_length": 34}
{"curie": "UMLS:C0854786", "names": ["Metastatic Small Bowel Carcinoma", "Metastatic Small Intestine Cancer", "Metastatic Small Intestinal Cancer", "Small intestine carcinoma metastatic", "Metastatic Small Intestinal Carcinoma", "Metastatic Carcinoma from the Small Bowel", "Metastatic Carcinoma from the Small Intestine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small intestine carcinoma metastatic", "shortest_name_length": 32}
{"curie": "MONDO:0004663", "names": ["Colon cancer stage 0", "Stage 0 Colon Cancer", "stage 0 colon cancer", "Colon Cancer Stage 0", "colon cancer stage 0", "colon cancer, stage 0", "Colon carcinoma stage 0", "Stage 0 Colon Carcinoma", "stage 0 colon carcinoma", "Cancer in situ of colon", "colon carcinoma in situ", "Colon Carcinoma in situ", "colon in situ carcinoma", "COLON NOS CANCER IN SITU", "stage 0 colonic carcinoma", "Stage 0 Colonic Carcinoma", "stage 0 Colonic carcinoma", "Colonic carcinoma in situ", "Colonic Carcinoma in situ", "colonic carcinoma in situ", "Carcinoma in situ of Colon", "stage 0 carcinoma of colon", "carcinoma in situ of colon", "Carcinoma in situ of colon", "Stage 0 Carcinoma of Colon", "Stage 0 Colon Cancer AJCC v6", "Stage 0 Colon Cancer AJCC v7", "stage 0 colon cancer aJCC v6", "stage 0 colon cancer aJCC v7", "Stage 0 Carcinoma of the Colon", "Carcinoma in situ of the Colon", "carcinoma in situ of the colon", "stage 0 carcinoma of the colon", "Carcinoma in situ of colon, NOS", "stage 0 colon cancer aJCC v6 and v7", "Stage 0 Colon Cancer AJCC v6 and v7", "Carcinoma in situ of colon (disorder)", "carcinoma in situ of colon (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colon carcinoma in situ", "shortest_name_length": 20}
{"curie": "UMLS:C1334052", "names": ["HPVA Cervical Squamous Cell Carcinoma", "HPV-Related Cervical Squamous Cell Carcinoma", "HPV-Associated Cervical Squamous Cell Carcinoma", "Human Papillomavirus-Related Cervical Squamous Cell Carcinoma", "Human Papilloma Virus-Related Cervical Squamous Cell Carcinoma", "Human Papilloma Virus Related Cervical Squamous Cell Carcinoma", "Human Papillomavirus-Associated Cervical Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Human Papillomavirus-Related Cervical Squamous Cell Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0017248", "names": ["CPAM type 0", "congenital pulmonary airway malformation type 0", "congenital cystic adenomatoid malformation of the lung type 0", "congenital cystic adenomatous malformation of the lung type 0"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital pulmonary airway malformation type 0", "shortest_name_length": 11}
{"curie": "UMLS:C0422853", "names": ["Olfactory Seizure", "Olfactory seizure", "Seizure, Olfactory", "Olfactory Seizures", "Seizures, Olfactory", "Olfactory uncinate fit", "Uncinate fit, olfactory", "Olfactory seizure (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Olfactory seizure", "shortest_name_length": 17}
{"curie": "UMLS:C0026936", "names": ["mycoplasma", "Mycoplasma", "mycoplasmosis", "Mycoplasmosis", "Mycoplasmosis, NOS", "Mycoplasma Infection", "MYCOPLASMA INFECTION", "mycoplasma infection", "Mycoplasma infection", "mycoplasma infections", "infection; Mycoplasma", "Mycoplasma infections", "MYCOPLASMA INFECTIONS", "Mycoplasma; infection", "Infection, Mycoplasma", "Mycoplasma Infections", "Infection by PPLO, NOS", "Infections, Mycoplasma", "Mycoplasma infection NOS", "Disease caused by mycoplasma", "Infection by Mycoplasma, NOS", "Mycoplasma infection (disorder)", "Mycoplasma infection (diagnosis)", "Mycoplasma infection, unspecified", "Disease caused by Mycoplasma, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mycoplasma Infections", "shortest_name_length": 10}
{"curie": "MONDO:0002866", "names": ["Duodenal disease", "Duodenal Disease", "duodenum disease", "duodenal disease", "duodenal disorder", "diseases duodenum", "Duodenal Diseases", "Disease, Duodenal", "duodenal diseases", "duodenum; disease", "duodenum disorder", "Diseases, Duodenal", "disorders duodenum", "Duodenum--Diseases", "disease of duodenum", "Disease of duodenum", "disorder of duodenum", "Disorder of duodenum", "diseases of the duodenum", "DISEASES OF THE DUODENUM", "Disease of duodenum, NOS", "duodenum disease or disorder", "Disorder of duodenum (disorder)", "disease or disorder of duodenum", "disease (or disorder); duodenum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "duodenal disorder", "shortest_name_length": 16}
{"curie": "UMLS:C5237067", "names": ["Recurrent Very High-Risk Myelodysplastic Syndrome", "Recurrent Very High Risk Myelodysplastic Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Very High Risk Myelodysplastic Syndrome", "shortest_name_length": 49}
{"curie": "MONDO:0016825", "names": ["MMLA", "MITOCHONDRIAL MYOPATHY WITH LACTIC ACIDOSIS", "mitochondrial myopathy with lactic acidosis", "Mitochondrial myopathy with lactic acidosis", "mitochondrial myopathy-lactic acidosis-deafness syndrome", "mitochondrial myopathy-lactic acidosis-hearing loss syndrome", "metabolic myopathy associated with chronic lactic acidemia, growth failure, and nerve deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial myopathy-lactic acidosis-deafness syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0012518", "names": ["CMS12", "CMSTA1", "congenital myasthenic syndrome 12", "Congenital Myasthenic Syndrome 12", "MYASTHENIC SYNDROME, CONGENITAL, 12", "myasthenic syndrome, congenital, 12", "congenital myasthenic syndrome type 12", "myasthenic syndrome, congenital, type 12", "congenital myasthenia 12 with tubular aggregates", "myasthenia, congenital, 12, with tubular aggregates", "MYASTHENIC SYNDROME, CONGENITAL, WITH TUBULAR AGGREGATES 1", "myasthenic syndrome, congenital, with tubular aggregates 1", "GFPT1 congenital myasthenic syndromes with glycosylation defect", "congenital myasthenic syndromes with glycosylation defect caused by mutation in GFPT1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myasthenic syndrome 12", "shortest_name_length": 5}
{"curie": "MONDO:0007874", "names": ["LGS", "TRPS2", "TRPS 2", "TRPSII", "Deletion 8q24.1", "deletion 8q24.1", "monosomy 8q24.1", "Monosomy 8q24.1", "Acrodysplasia V", "Acrodysplasia Vs", "Ale-Calo syndrome", "Giedion-Langer Syndrome", "Giedion Langer Syndrome", "LANGER-GIEDION SYNDROME", "Langer Giedion Syndrome", "langer-giedion syndrome", "giedion langer syndrome", "Giedion-Langer syndrome", "Langer-Giedion syndrome", "Langer-Giedion Syndrome", "Langer Giedion syndrome", "langer giedion syndrome", "Syndrome, Giedion-Langer", "Syndrome, Langer-Giedion", "Trigorhinophalangeal dysplasia", "trichorhinophalangeal syndrome 2", "Trichorhinophalangeal syndrome II", "trichorhinophalangeal dysplasia 2", "acrodysplasia-dysostoses syndrome", "Langer-Giedion syndrome (disorder)", "CHROMOSOME 8q24.1 DELETION SYNDROME", "Langer-Giedion syndrome (diagnosis)", "chromosome 8Q24.1 deletion syndrome", "Trichorhinophalangeal Syndrome Type 2", "trichorhinophalangeal syndrome type 2", "Trichorhinophalangeal syndrome type 2", "trichorhinophalangeal syndrome, type 2", "trichorhinophalangeal syndrome type II", "Trichorhinophalangeal Syndrome Type II", "TRICHORHINOPHALANGEAL SYNDROME, TYPE II", "trichorhinophalangeal dysplasia type II", "Trichorhinophalangeal Syndrome, Type II", "Trichorhinophalangeal dysplasia type II", "trichorhinophalangeal syndrome, type II", "Tricho-Rhino-Phalangeal Syndrome Type II", "Tricho Rhino Phalangeal Syndrome Type II", "TRPS II - Trichorhinophalangeal syndrome II", "Trichorhinophalangeal syndrome with exostosis", "Trichorhinophalangeal Syndrome with Exostoses", "trichorhinophalangeal (TRP) syndrome 2 (TRPS2)", "multiple exostoses-mental retardation syndrome", "Langer-Giedion type of trichorhinophalangeal syndrome", "multiple exostoses-mental retardation (MEMR) syndrome", "trichorhino-auriculophalangeal multiple exostoses dysplasia", "trichorhino-auriculophalangeal multiple exostoses (TRAMPE) dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichorhinophalangeal syndrome type II", "shortest_name_length": 3}
{"curie": "MONDO:0014556", "names": ["CLIFAHDD", "CLIFAHDD syndrome", "Congenital limbs-face contractures-hypotonia-developmental delay syndrome", "congenital limbs-face contractures-hypotonia-developmental delay syndrome", "CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY", "Congenital contracture of limbs and face, hypotonia, developmental delay syndrome", "congenital contractures of the limbs and face, hypotonia, and developmental delay", "CLIFAHDD (congenital limbs, face contractures, hypotonia, developmental delay) syndrome", "Congenital contracture of limbs and face, hypotonia, developmental delay syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital contractures of the limbs and face, hypotonia, and developmental delay", "shortest_name_length": 8}
{"curie": "UMLS:C4086155", "names": ["Childhood Choriocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Choriocarcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0014766", "names": ["LDAMD", "LEUKODYSTROPHY AND ACQUIRED MICROCEPHALY WITH OR WITHOUT DYSTONIA", "leukodystrophy and acquired microcephaly with or without dystonia", "leukodystrophy and acquired microcephaly with or without dystonia;"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukodystrophy and acquired microcephaly with or without dystonia;", "shortest_name_length": 5}
{"curie": "UMLS:C1707299", "names": ["Heart Inflammatory Myofibroblastic Tumor", "Cardiac Inflammatory Myofibroblastic Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiac Inflammatory Myofibroblastic Tumor", "shortest_name_length": 40}
{"curie": "MONDO:0022771", "names": ["circumscribed disseminated keratosis Jadassohn lew type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "circumscribed disseminated keratosis Jadassohn lew type", "shortest_name_length": 55}
{"curie": "MONDO:0018188", "names": ["genetic intestinal polyposis", "Genetic intestinal polyposis", "Familial Intestinal Polyposis", "familial intestinal polyposis", "Familial Intestinal Polyposes", "Familial intestinal polyposis", "Intestinal Polyposes, Familial", "Intestinal Polyposis, Familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genetic intestinal polyposis", "shortest_name_length": 28}
{"curie": "MONDO:0001490", "names": ["Granular corneal dystrophy", "corneal dystrophy granular", "Corneal Granular Dystrophy", "Granular Corneal Dystrophy", "corneal granular dystrophy", "granular corneal dystrophy", "Dystrophy, Corneal Granular", "Granular Dystrophy, Corneal", "Corneal Granular Dystrophies", "Granular corneal dystrophy (disorder)", "granular corneal dystrophy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal granular dystrophy", "shortest_name_length": 26}
{"curie": "MONDO:0010382", "names": ["FXTAS", "Fxtas", "FXTAS syndrome", "Fragile X Tremor Ataxia Syndrome", "Fragile X Tremor/Ataxia Syndrome", "FRAGILE X TREMOR/ATAXIA SYNDROME", "fragile X tremor/ataxia syndrome", "fragile 10 tremor/ataxia syndrome", "FXTAS Fragile X Tremor Ataxia Syndrome", "fragile X-associated tremor/ataxia syndrome", "Fragile X associated tremor ataxia syndrome", "Fragile X-Associated Tremor Ataxia Syndrome", "Fragile X-associated tremor/ataxia syndrome", "Fragile X tremor/ataxia syndrome, X-linked dominant", "Fragile X associated tremor ataxia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fragile X-associated tremor/ataxia syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0001724", "names": ["supraglottis", "supraglottis cancer", "Ca larynx - supraglottis", "Malignant Supraglottis Tumor", "malignant supraglottic tumor", "Malignant Supraglottic Tumor", "malignant supraglottis tumor", "malignant Supraglottic tumor", "SUPRAGLOTTIC CANCER MALIGNANT", "Malignant Supraglottis Neoplasm", "malignant supraglottal neoplasm", "Malignant Tumor of Supraglottis", "malignant tumor of supraglottis", "malignant supraglottic neoplasm", "Malignant Supraglottic Neoplasm", "Malignant tumor of supraglottis", "malignant supraglottis neoplasm", "Malignant tumour of supraglottis", "malignant neoplasm of supraglottis", "Malignant Neoplasm of Supraglottis", "Malignant neoplasm of supraglottis", "supraglottic part of larynx cancer", "malignant tumor of the supraglottis", "Malignant Tumor of the Supraglottis", "cancer of supraglottic part of larynx", "Malignant Neoplasm of the Supraglottis", "malignant neoplasm of the supraglottis", "malignant neoplasm of extrinsic larynx", "Malignant neoplasm of extrinsic larynx", "Malignant tumor of supraglottis (disorder)", "malignant neoplasm of supraglottis (diagnosis)", "malignant supraglottic part of larynx neoplasm", "malignant neoplasm of supraglottic part of larynx"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "supraglottis cancer", "shortest_name_length": 12}
{"curie": "UMLS:C0278747", "names": ["Localized GI Carcinoid Tumor", "Localized Digestive Carcinoid Tumor", "Localized Gastrointestinal Carcinoid Tumor", "localized gastrointestinal carcinoid tumor", "gastrointestinal carcinoid tumor, localized", "Localized Gastrointestinal Neuroendocrine Tumor G1", "Localized Digestive System Neuroendocrine Tumor G1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized Digestive System Neuroendocrine Tumor G1", "shortest_name_length": 28}
{"curie": "UMLS:C0549225", "names": ["Myasthenic syndrome", "Myasthenic Syndrome", "MYASTHENIC SYNDROME", "myasthenic syndrome", "syndrome; myasthenic", "myasthenic syndromes", "myasthenic; syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myasthenic Syndrome", "shortest_name_length": 19}
{"curie": "UMLS:C2987193", "names": ["Pancreatic Intraductal Papillary Mucinous Neoplasm, Intestinal-Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Intraductal Papillary Mucinous Neoplasm, Intestinal-Type", "shortest_name_length": 67}
{"curie": "MONDO:0016516", "names": ["KCS2", "KENNY SYNDROME", "Kenny syndrome", "kenny syndrome", "Kenny's syndrome", "kenny's syndrome", "Kenny Caffey syndrome", "kenny caffey syndrome", "Kenny-Caffey Syndrome", "Kenny-Caffey syndrome", "kenny-caffey syndrome", "Kenny-Linarelli syndrome", "Kenny syndrome (disorder)", "congenital tubular stenosis", "Kenny-Caffey syndrome (KCS)", "Kenny-Caffey Syndrome Type 2", "Kenny-Caffey syndrome, type 2", "KENNY-CAFFEY SYNDROME, TYPE 2", "Kenny-Caffey syndrome (diagnosis)", "dwarfism-congenital medullary stenosis syndrome", "dwarfism and cortical thickening of tubular bones", "hypocalcemia-dwarfism-cortical thickening syndrome", "Dwarfism, cortical thickening of tubular bones, and transient hypocalcemia", "DWARFISM, CORTICAL THICKENING OF TUBULAR BONES, AND TRANSIENT HYPOCALCEMIA", "dwarfism-cortical thickening of tubular bones-transient hypocalcemia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kenny-Caffey syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0010908", "names": ["loose anagen syndrome", "Loose anagen syndrome", "Loose Anagen Syndrome", "Syndrome, Loose Anagen", "Loose Anagen Syndromes", "Anagen Syndrome, Loose", "Anagen Syndromes, Loose", "Syndromes, Loose Anagen", "LOOSE ANAGEN HAIR SYNDROME", "loose anagen hair syndrome", "Loose anagen hair syndrome", "Loose Anagen Hair Syndrome", "Loose anagen hair syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "loose anagen syndrome", "shortest_name_length": 21}
{"curie": "MONDO:0011177", "names": ["HNED", "PHNED", "ECTD4", "ectodermal dysplasia 4", "pili torti onychodysplasia", "Hair-nail ectodermal dysplasia", "twisted hair with nail dysplasias", "ectodermal dysplasia 4, hair/nail type", "ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE", "Pure hair and nail ectodermal dysplasia", "Ectodermal Dysplasia, Pure Hair-Nail Type", "ectodermal dysplasia, 'Pure' hair/nail type", "ECTODERMAL DYSPLASIA, 'PURE' HAIR/NAIL TYPE", "KRT85 pure hair and nail ectodermal dysplasia", "pure hair and nail ectodermal dysplasia caused by mutation in KRT85"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia 4, hair/nail type", "shortest_name_length": 4}
{"curie": "MONDO:0030498", "names": ["IMD92", "IMMUNODEFICIENCY 92", "immunodeficiency 92", "immunodeficiency due to REL deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 92", "shortest_name_length": 5}
{"curie": "MONDO:0021400", "names": ["Colon Polyp", "colon polyp", "Polyp colon", "COLON POLYP", "polyp; colon", "colon polyps", "polyps colon", "Colon polyps", "Colon Polyps", "colon; polyp", "colonic polyp", "COLONIC POLYP", "Colonic Polyp", "Colonic polyp", "Polyp(s);colon", "Colonic polyps", "Colonic Polyps", "Polyp of Colon", "Polyp of colon", "colonic polyps", "Polyp, Colonic", "polyp of colon", "Polyps, Colonic", "polyps of colon", "COLON NOS POLYP", "Colonic polyp, NOS", "Polyp of the Colon", "polyp of the colon", "Polyp of colon, NOS", "Polyp of colon (disorder)", "polyps of colon (diagnosis)", "Colonic polyp(s) (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyp of colon", "shortest_name_length": 11}
{"curie": "UMLS:C2721603", "names": ["Henoch-Schonlein purpura nephritis", "Henoch-Schönlein Purpura Nephritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Henoch-Schonlein purpura nephritis", "shortest_name_length": 34}
{"curie": "MONDO:0018340", "names": ["hereditary isolated aplastic anemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary isolated aplastic anemia", "shortest_name_length": 35}
{"curie": "MONDO:0013532", "names": ["protein Z deficiency", "protein z deficiency", "PROTEIN Z DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "protein Z deficiency", "shortest_name_length": 20}
{"curie": "MONDO:0010694", "names": ["myoclonic nystagmus", "Nystagmus, Myoclonic", "nystagmus, myoclonic", "NYSTAGMUS, MYOCLONIC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nystagmus, myoclonic", "shortest_name_length": 19}
{"curie": "UMLS:C1305904", "names": ["Familial hematuria", "Familial haematuria", "Familial hematuria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Familial hematuria", "shortest_name_length": 18}
{"curie": "UMLS:C1708780", "names": ["Lung Pleomorphic Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Pleomorphic Adenoma", "shortest_name_length": 24}
{"curie": "MONDO:0015699", "names": ["immunodeficiency due to an early component of complement deficiency", "immunodeficiency due to C1, C4, or C2 component complement deficiency", "immunodeficiency due to a C1, C4, or C2 component complement deficiency", "immunodeficiency due to a classical component pathway complement deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency due to a classical component pathway complement deficiency", "shortest_name_length": 67}
{"curie": "MONDO:0002309", "names": ["Papillary conjunctivitis", "Conjunctivitis papillary", "papillary conjunctivitis", "Papillary Conjunctivitis", "Papillary conjunctivitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papillary conjunctivitis", "shortest_name_length": 24}
{"curie": "MONDO:0002882", "names": ["colon NET", "Colonic NET", "NET of the colon", "colon neuroendocrine tumor", "colonic neuroendocrine tumor", "Colonic neuroendocrine tumor", "colon neuroendocrine neoplasm", "Colon Neuroendocrine Neoplasm", "colonic neuroendocrine neoplasm", "Colonic Neuroendocrine Neoplasm", "Neuroendocrine neoplasm of colon", "Neuroendocrine Neoplasm of Colon", "neuroendocrine neoplasm of colon", "Neuroendocrine tumor of the colon", "neuroendocrine tumor of the colon", "Neuroendocrine Neoplasm of the Colon", "Neuroendocrine neoplasm of the colon", "neuroendocrine neoplasm of the colon", "Neuroendocrine neoplasm of colon (disorder)", "colon neuroendocrine tumor, well differentiated, low or intermediate grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colon neuroendocrine neoplasm", "shortest_name_length": 9}
{"curie": "MONDO:0100421", "names": ["AML, GATA1 Mutation", "AML, GF1 Gene Mutation", "AML, GF-1 Gene Mutation", "AML, NFE1 Gene Mutation", "AML, ERYF1 Gene Mutation", "AML, NF-E1 Gene Mutation", "AML, GATA1 gene mutation", "AML, GATA-1 Gene Mutation", "AML, GATA Binding Protein 1 Gene Mutation", "acute myeloid leukemia, GATA1 gene mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, GATA1 gene mutation", "shortest_name_length": 19}
{"curie": "MONDO:0003731", "names": ["Adult CNS Teratoma", "adult CNS teratoma", "Teratoma of Adult CNS", "teratoma of adult CNS", "teratoma of the adult CNS", "Teratoma of the Adult CNS", "Central Nervous System Teratoma", "Central nervous system teratoma", "Adult Central Nervous System Teratoma", "adult central nervous system teratoma", "Teratoma of Adult Central Nervous System", "teratoma of adult central nervous system", "central nervous system teratoma of adults", "Teratoma of the Adult Central Nervous System", "teratoma of the adult central nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult central nervous system teratoma", "shortest_name_length": 18}
{"curie": "MONDO:0027767", "names": ["simons syndrome", "Partial Lipodystrophy", "Partial lipodystrophy", "PARTIAL LIPODYSTROPHY", "partial lipodystrophy", "acquired partial lipodystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial lipodystrophy", "shortest_name_length": 15}
{"curie": "UMLS:C4520901", "names": ["Stage 0 Hypopharynx Epidermoid Carcinoma", "Hypopharynx Epidermoid Carcinoma in situ", "Stage 0 Epidermoid Carcinoma of Hypopharynx", "Hypopharyngeal Epidermoid Carcinoma in situ", "Stage 0 Hypopharynx Squamous Cell Carcinoma", "Epidermoid Carcinoma in situ of Hypopharynx", "Hypopharynx Squamous Cell Carcinoma in situ", "Stage 0 Hypopharyngeal Epidermoid Carcinoma", "Stage 0 Squamous Cell Carcinoma of Hypopharynx", "Stage 0 Hypopharyngeal Squamous Cell Carcinoma", "Squamous Cell Carcinoma in situ of Hypopharynx", "Hypopharyngeal Squamous Cell Carcinoma in situ", "Stage 0 Epidermoid Carcinoma of the Hypopharynx", "Epidermoid Carcinoma in situ of the Hypopharynx", "Squamous Cell Carcinoma in situ of the Hypopharynx", "Stage 0 Squamous Cell Carcinoma of the Hypopharynx", "Stage 0 Hypopharyngeal Throat Squamous Cell Cancer", "Stage 0 Hypopharyngeal Squamous Cell Carcinoma AJCC v6", "Stage 0 Hypopharyngeal Squamous Cell Carcinoma AJCC v8", "Stage 0 Hypopharyngeal Squamous Cell Carcinoma AJCC v7", "Stage 0 Hypopharyngeal Squamous Cell Carcinoma AJCC v6, v7, and v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Hypopharyngeal Squamous Cell Carcinoma AJCC v6, v7, and v8", "shortest_name_length": 40}
{"curie": "MONDO:0019133", "names": ["visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome", "shortest_name_length": 83}
{"curie": "MONDO:0003671", "names": ["Septal myocardial infarction", "MYOCARDIAL INFARCTION SEPTAL", "septal myocardial infarction", "infarction myocardial septal", "cardiac septum myocardial infarction (disease)", "myocardial infarction (disease) of cardiac septum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "septal myocardial infarction", "shortest_name_length": 28}
{"curie": "UMLS:C4289034", "names": ["Glioblastoma with PNET-Like Component", "Glioblastoma with Primitive Neuronal Component"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Glioblastoma with Primitive Neuronal Component", "shortest_name_length": 37}
{"curie": "MONDO:0060642", "names": ["NEDMAGA", "NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES", "neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features", "shortest_name_length": 7}
{"curie": "UMLS:C1336894", "names": ["Urinary Tract Paraganglioma", "Urinary System Paraganglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urinary System Paraganglioma", "shortest_name_length": 27}
{"curie": "MONDO:0002633", "names": ["cranial nerve tumor", "Cranial Nerve Tumor", "cranial nerves tumors", "Cranial Nerve Neoplasm", "cranial nerve neoplasm", "Tumor of Cranial Nerve", "tumor of cranial nerve", "Cranial nerve neoplasm", "Tumor of cranial nerve", "Tumour of cranial nerve", "Neoplasm, Cranial Nerve", "cranial nerve neoplasms", "Cranial Nerve Neoplasms", "Neoplasms, Cranial Nerve", "Neoplasm of Cranial Nerve", "neoplasm of cranial nerve", "Neoplasm of cranial nerve", "Tumor of the Cranial Nerve", "tumor of the cranial nerve", "Neoplasm of the Cranial Nerve", "neoplasm of the cranial nerve", "cranial nerve neoplasm (disease)", "Neoplasm of cranial nerve (disorder)", "neoplasm of cranial nerve (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cranial nerve neoplasm", "shortest_name_length": 19}
{"curie": "MONDO:0015720", "names": ["moderately severe hemophilia A", "moderately severe hemophilia type A", "moderately severe factor VIII deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "moderately severe hemophilia A", "shortest_name_length": 30}
{"curie": "MONDO:0018951", "names": ["MPD2", "VCPDM", "distal myopathy 2", "MATR3-related distal myopathy", "distal myopathy with vocal cord weakness", "vocal cord and pharyngeal distal myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal myopathy with vocal cord weakness", "shortest_name_length": 4}
{"curie": "MONDO:0008904", "names": ["Campomelic syndrome long limb type", "campomelic syndrome long limb type", "campomelic syndrome, long-limb type", "Campomelic Syndrome, Long-Limb Type", "CAMPOMELIC SYNDROME, LONG-LIMB TYPE", "Camptomelic syndrome long limb type", "Camptomelic Syndrome, Long-Limb Type", "CAMPTOMELIC SYNDROME, LONG-LIMB TYPE", "camptomelic syndrome, long-limb type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "camptomelic syndrome, long-limb type", "shortest_name_length": 34}
{"curie": "MONDO:0003356", "names": ["Epithelioid Leiomyosarcoma", "Epithelioid leiomyosarcoma", "epithelioid leiomyosarcoma", "Epithelioid Leiomyosarcomas", "Leiomyosarcoma, Epithelioid", "Leiomyosarcomas, Epithelioid", "epithelioid leiomyosarcoma (diagnosis)", "Epithelioid leiomyosarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epithelioid leiomyosarcoma", "shortest_name_length": 26}
{"curie": "MONDO:0030015", "names": ["BMFS6", "bone marrow failure syndrome 6", "BONE MARROW FAILURE SYNDROME 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bone marrow failure syndrome 6", "shortest_name_length": 5}
{"curie": "UMLS:C5669921", "names": ["Infant-Type Hemispheric Glioma, ROS1-Altered"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infant-Type Hemispheric Glioma, ROS1-Altered", "shortest_name_length": 44}
{"curie": "MONDO:0024536", "names": ["GCCD1", "ACTH resistance", "glucocorticoid deficiency 1", "adrenal unresponsiveness to ACTH", "familial glucocorticoid deficiency 1", "MC2R familial glucocorticoid deficiency", "glucocorticoid deficiency, due to ACTH unresponsiveness", "familial glucocorticoid deficiency caused by mutation in MC2R"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glucocorticoid deficiency 1", "shortest_name_length": 5}
{"curie": "MONDO:0021039", "names": ["extraosseous Ewing's tumor", "extraosseous Ewing's tumour", "extraosseous Ewings sarcoma-primitive neuroepithelial tumor", "extraosseous Ewings sarcoma-primitive neuroepithelial tumour", "Extraosseous Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor", "extraosseous Ewing sarcoma/peripheral primitive neuroectodermal tumor", "Extraskeletal Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor", "extraskeletal Ewing sarcoma/peripheral primitive neuroectodermal tumor", "extraosseous Ewing's sarcoma/peripheral primitive neuroectodermal tumor", "Extraosseous Ewing's Sarcoma/Peripheral Primitive Neuroectodermal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extraskeletal Ewing sarcoma/peripheral primitive neuroectodermal tumor", "shortest_name_length": 26}
{"curie": "MONDO:0013149", "names": ["HYDROPS FETALIS, NONIMMUNE, WITH GRACILE BONES AND DYSMORPHISM", "hydrops fetalis, nonimmune, with gracile bones and dysmorphic features", "Hydrops Fetalis, Nonimmune, With Gracile Bones And Dysmorphic Features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hydrops fetalis, nonimmune, with gracile bones and dysmorphic features", "shortest_name_length": 62}
{"curie": "MONDO:0015753", "names": ["Cap Disease", "Cap disease", "Cap Myopathy", "Cap myopathy", "cap myopathy", "Cap myopathy (disorder)", "Congenital myopathy with caps", "congenital myopathy with caps", "Congenital Myopathy with Caps"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cap myopathy", "shortest_name_length": 11}
{"curie": "MONDO:0010403", "names": ["ALDS", "ADFN", "Woolf syndrome", "Woolf's syndrome", "albinism-deafness syndrome", "Albinism-deafness syndrome", "ALBINISM-DEAFNESS SYNDROME", "albinism deafness syndrome", "Albinism-Deafness Syndrome", "Albinism deafness syndrome", "Woolf's syndrome (disorder)", "Ziprkowski–Margolis syndrome", "albinism-hearing loss syndrome", "Albinism-hearing loss syndrome", "Albinism with deafness syndrome", "Albinism with deafness syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "albinism-hearing loss syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C3897007", "names": ["Neonatal Herpes Simplex Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neonatal Herpes Simplex Infection", "shortest_name_length": 33}
{"curie": "MONDO:0015414", "names": ["CLEFT NOSE", "Alar cleft", "alar cleft", "cleft nose", "Cleft nose", "cleft; nose", "nose; cleft", "Alar rim cleft", "alar rim cleft", "Congenital cleft nose", "Tessier number 1 cleft", "cleft nose (diagnosis)", "Paramedian nasal cleft", "paramedian nasal cleft", "isolated coloboma of the nose", "Isolated coloboma of the nose", "cleft nose (physical finding)", "isolated cleft of the ala nasi", "Isolated cleft of the ala nasi", "Congenital cleft nose (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paramedian nasal cleft", "shortest_name_length": 10}
{"curie": "MONDO:0004622", "names": ["ischemia; bowel, chronic", "chronic intestinal ischemia", "chronic mesenteric ischemia", "Chronic mesenteric ischemia", "Chronic intestinal ischemia", "Chronic intestinal ischaemia", "Chronic mesenteric ischaemia", "CMI - Chronic mesenteric ischemia", "CMI - Chronic mesenteric ischaemia", "CMI - chronic mesenteric ischaemia", "Chronic intestinal ischemic syndrome", "Chronic intestinal ischaemic syndrome", "Chronic intestinal vascular insufficiency", "Chronic intestinal ischemic syndrome, NOS", "chronic intestinal vascular insufficiency", "MESENTERIC VASCULAR INSUFFICIENCY, CHRONIC", "Chronic intestinal ischaemic syndrome, NOS", "Chronic vascular insufficiency of intestine", "Chronic vascular insufficiency of intestine, NOS", "Chronic mesenteric arterial insufficiency syndrome", "Chronic vascular insufficiency of intestine (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic intestinal vascular insufficiency", "shortest_name_length": 24}
{"curie": "MONDO:0023510", "names": ["Jaffer Beighton syndrome", "Jaffer-Beighton syndrome", "arachnodactyly, joint laxity, and spondylolisthesis", "Arachnodactyly, joint laxity, and spondylolisthesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jaffer-Beighton syndrome", "shortest_name_length": 24}
{"curie": "UMLS:C1328361", "names": ["Low turnover osteopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low turnover osteopathy", "shortest_name_length": 23}
{"curie": "MONDO:0016546", "names": ["OT", "POT", "pot", "shaky leg syndrome", "Shaky leg syndrome", "primary orthostatic tremor", "orthostatic tremor primary", "Primary orthostatic tremor", "Orthostatic tremor, primary", "orthostatic tremor, primary", "POT - Primary orthostatic tremor", "Primary orthostatic tremor (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary orthostatic tremor", "shortest_name_length": 2}
{"curie": "UMLS:C1708784", "names": ["Lung Spindle Cell Carcinoma", "Spindle cell carcinoma of lung", "spindle cell carcinoma of lung", "Spindle cell carcinoma of the lung", "Spindle cell carcinoma of lung (disorder)", "spindle cell carcinoma of lung (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Spindle Cell Carcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0013499", "names": ["FANCP", "SLX4 Fanconi anemia", "Slx4 Fanconi anemia", "Fanconi anemia complementation group P", "Fanconi anemia, complementation group P", "FANCONI ANEMIA, COMPLEMENTATION GROUP P", "Fanconi anemia caused by mutation in SLX4", "Fanconi anemia caused by mutation in Slx4", "Fanconi anemia complementation group type P", "Fanconi Anemia, complementation group type P", "Fanconi anemia complementation group P (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fanconi anemia complementation group P", "shortest_name_length": 5}
{"curie": "MONDO:0004561", "names": ["retina melanoma", "retina; melanoma", "melanoma; retina", "Retinal Melanoma", "Retinal melanoma", "retinal melanoma", "Melanoma of retina", "melanoma of retina", "Melanoma of Retina", "Melanoma of the Retina", "melanoma of the retina", "retina melanoma (disease)", "malignant retinal melanoma", "malignant Retinal melanoma", "Malignant Retinal Melanoma", "malignant melanoma of retina", "Malignant Melanoma of Retina", "melanoma (disease) of retina", "Malignant melanoma of retina", "Malignant Melanoma of the Retina", "malignant melanoma of the retina", "retinal neoplasm malignant melanoma", "Malignant melanoma of retina (disorder)", "malignant melanoma of the retina (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal melanoma", "shortest_name_length": 15}
{"curie": "MONDO:0003899", "names": ["Adult Myxoid Chondrosarcoma", "adult myxoid chondrosarcoma", "myxoid chondrosarcoma of adults", "adult extraosseous chondrosarcoma", "adult extraskeletal chondrosarcoma", "Extraskeletal Myxoid Chondrosarcoma", "chondrosarcoma, adult extraskeletal", "extraskeletal chondrosarcoma, adult", "Adult Extraosseous Myxoid Chondrosarcoma", "Adult Extraskeletal Myxoid Chondrosarcoma", "adult extraskeletal myxoid chondrosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult myxoid chondrosarcoma", "shortest_name_length": 27}
{"curie": "UMLS:C2910233", "names": ["Superior Vesical Fissure", "bladder exstrophy supravesical fissure", "Supravesical Fissure of Urinary Bladder", "supravesical fissure of urinary bladder", "Supravesical fissure of urinary bladder", "supravesical fissure of urinary bladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "supravesical fissure of urinary bladder", "shortest_name_length": 24}
{"curie": "MONDO:0017677", "names": ["Focal acral hyperkeratosis", "focal acral hyperkeratosis", "PPPK3 without elastoidosis", "PPKP3 without elastoidosis", "Focal acral hyperkeratosis (disorder)", "focal acral hyperkeratosis (diagnosis)", "Punctate palmoplantar keratoderma type 3 without elastoidosis", "punctate palmoplantar keratoderma type 3 without elastoidosis", "punctate palmoplantar hyperkeratosis type 3 without elastoidosis", "Punctate palmoplantar hyperkeratosis type 3 without elastoidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal acral hyperkeratosis", "shortest_name_length": 26}
{"curie": "MONDO:0006821", "names": ["papillary necrosis", "necrosis papillary", "Papillary necrosis", "PAPILLARY NECROSIS", "Medullary necrosis", "papillary; necrosis", "medullary; necrosis", "necrosis; medullary", "necrosis; papillary", "Necrotizing papillitis", "Necrotising papillitis", "Renal Medullary Necrosis", "Renal papillary necrosis", "Renal Papillary Necrosis", "Necrosis;renal;papillary", "RENAL PAPILLARY NECROSIS", "PAPILLARY NECROSIS RENAL", "renal papillary necrosis", "Papillary necrosis renal", "renal medullary necrosis", "Renal medullary necrosis", "Necrosis papillary kidney", "Kidney Papillary Necrosis", "NECROSIS KIDNEY PAPILLARY", "Necrosis kidney papillary", "kidney papillary necrosis", "Papillary kidney necrosis", "PAPILLARY KIDNEY NECROSIS", "Necrosis, Renal Medullary", "NECROSIS PAPILLARY KIDNEY", "Necrosis, Kidney Papillary", "KIDNEY, PAPILLARY NECROSIS", "Papillary Necrosis, Kidney", "necrosis; kidney, papillary", "kidney; necrosis, papillary", "RENAL PAPILLITIS NECROTISING", "Papillitis renal necrotising", "PAPILLITIS RENAL NECROTIZING", "RENAL PAPILLITIS NECROTIZING", "Necrotising renal papillitis", "Necrotizing renal papillitis", "Papillitis renal necrotizing", "Renal papillitis necrotizing", "Necrotizing Renal Papillitis", "renal papillitis necrotizing", "Renal papillitis necrotising", "renal PAPILLITIS NECROTIZING", "necrotizing renal papillitis", "Renal Papillitis, Necrotizing", "Papillary necrosis (disorder)", "PAPILLITIS, RENAL, NECROTIZING", "Necrotizing Renal Papillitides", "papillary necrosis (diagnosis)", "Renal Papillitides, Necrotizing", "Papillitides, Necrotizing Renal", "renal medullary necrosis (diagnosis)", "nephropathy renal medullary necrosis", "Nephropathy NOS with renal medullary necrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kidney papillary necrosis", "shortest_name_length": 18}
{"curie": "MONDO:0009333", "names": ["Urioste syndrome", "URIOSTE SYNDROME", "Urioste Martinez-Frias syndrome", "Müllerian derivatives-lymphangiectasia-polydactyly syndrome", "mullerian derivatives-lymphangiectasia-polydactyly syndrome", "persistence of mullerian derivatives with lymphangiectasia and postaxial polydactyly", "MULLERIAN derivatives, persistence of, with lymphangiectasia and postaxial polydactyly", "MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY", "renal and craniofacial anomalies with persistence of mullerian derivatives, lymphangiectasis, hepatic failure, postaxial polydactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mullerian derivatives-lymphangiectasia-polydactyly syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0004509", "names": ["Intrahepatic Bile Duct IPN", "intrahepatic biliary papillomatosis", "Intrahepatic Biliary Papillomatosis", "Intrahepatic Bile Duct Papillomatosis", "intrahepatic bile duct papillomatosis", "Intrahepatic Bile Duct Papillary Neoplasm", "intrahepatic bile duct papillary neoplasm", "Intrahepatic Bile Duct Intraductal Papillary Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intrahepatic biliary papillomatosis", "shortest_name_length": 26}
{"curie": "MONDO:0032920", "names": ["JUVAR", "JUVENILE ARTHRITIS", "juvenile arthritis due to defect in LACC1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile arthritis due to defect in LACC1", "shortest_name_length": 5}
{"curie": "UMLS:C0009566", "names": ["complication", "Complication", "complications", "Complications", "Complication, NOS", "Other complication", "Medical Complication", "Medical complication", "medical complication", "complications medical"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Complication", "shortest_name_length": 12}
{"curie": "MONDO:0004178", "names": ["endodermal sinus pattern testicular yolk sac tumor", "Testicular Yolk Sac Tumor, Endodermal Sinus Pattern", "testicular yolk sac tumor, endodermal sinus pattern", "Testicular Yolk Sac Tumor, Endodermal Sinus/Perivascular Pattern"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular yolk sac tumor, endodermal sinus pattern", "shortest_name_length": 50}
{"curie": "UMLS:C0280189", "names": ["high-grade, relapsed adult NHL", "relapsed adult NHL, high grade", "adult NHL, relapsed, high grade", "recurrent adult NHL, high grade", "NHL, high grade, relapsed adult", "high-grade, recurrent adult NHL", "adult NHL, recurrent, high grade", "NHL, high grade, recurrent adult", "relapsed adult non-Hodgkin's lymphoma, high grade", "Recurrent High Grade Adult Non-Hodgkin's Lymphoma", "high-grade, relapsed adult non-Hodgkin's lymphoma", "recurrent adult non-Hodgkin's lymphoma, high grade", "lymphoma, high grade, relapsed adult non-Hodgkin's", "adult non-Hodgkin's lymphoma, high grade, relapsed", "non-Hodgkin's lymphoma, high grade, relapsed adult", "non-hodgkin's lymphoma, high grade, recurrent adult", "adult non-Hodgkin's lymphoma, high grade, recurrent", "lymphoma, high grade, recurrent adult non-Hodgkin's"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent High Grade Adult Non-Hodgkin's Lymphoma", "shortest_name_length": 30}
{"curie": "MONDO:0012229", "names": ["MYP9", "MYOPIA 9", "Myopia 9", "myopia 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopia 9", "shortest_name_length": 4}
{"curie": "MONDO:0011383", "names": ["ALPS2", "ALPS2A", "Type 2 ALPS", "ALPS-CASP10", "type 2 ALPS", "CASP10 autoimmune lymphoproliferative syndrome", "Type 2 Autoimmune Lymphoproliferative Syndrome", "type 2 autoimmune lymphoproliferative syndrome", "autoimmune lymphoproliferative syndrome type 2A", "autoimmune lymphoproliferative syndrome, type 2", "autoimmune lymphoproliferative syndrome, type 2A", "autoimmune lymphoproliferative syndrome type IIA", "autoimmune lymphoproliferative syndrome, type II", "AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE II", "autoimmune lymphoproliferative syndrome, type IIA", "Autoimmune Lymphoproliferative Syndrome, Type IIA", "AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA", "Autoimmune Lymphoproliferative Syndrome-CASP10 variant", "autoimmune lymphoproliferative syndrome-CASP10 variant", "autoimmune lymphoproliferative syndrome caused by mutation in CASP10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune lymphoproliferative syndrome type 2A", "shortest_name_length": 5}
{"curie": "UMLS:C0855628", "names": ["Stage I Supradiaphragmatic Nodular Sclerosis Hodgkin Lymphoma", "Hodgkin's disease nodular sclerosis stage I supradiaphragmatic", "Stage I Supradiaphragmatic Nodular Sclerosis Hodgkin's Disease", "Stage I Supradiaphragmatic Nodular Sclerosis Hodgkin's Lymphoma", "Stage I Nodular Sclerosis Hodgkin's Disease above the Diaphragm", "Stage I Nodular Sclerosis Hodgkin's Lymphoma above the Diaphragm", "Stage I Supradiaphragmatic Nodular Sclerosis Classical Hodgkin Lymphoma", "Ann Arbor Stage I Supradiaphragmatic Nodular Sclerosis Classic Hodgkin Lymphoma", "Ann Arbor Stage I Supradiaphragmatic Nodular Sclerosis Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's disease nodular sclerosis stage I supradiaphragmatic", "shortest_name_length": 61}
{"curie": "MONDO:0007493", "names": ["DYT4", "torsion dystonia 4", "whispering dysphonia", "torsion dystonia type 4", "Primary dystonia type 4", "Primary dystonia DYT4 type", "Primary dystonia, DYT4 type", "primary dystonia, DYT4 type", "Hereditary whispering dysphonia", "DYSTONIA MUSCULORUM DEFORMANS 4", "hereditary whispering dysphonia", "Dystonia musculorum deformans 4", "dystonia musculorum deformans 4", "whispering dysphonia, hereditary", "Whispering dysphonia, hereditary", "WHISPERING DYSPHONIA, HEREDITARY", "Primary dystonia type 4 (disorder)", "autosomal dominant torsion dystonia-4", "dystonia 4, torsion, autosomal dominant", "DYSTONIA 4, TORSION, AUTOSOMAL DOMINANT", "Dystonia 4, Torsion, Autosomal Dominant", "Torsion dystonia 4, autosomal dominant type", "DYSTONIA 4, TORSION, AUTOSOMAL DOMINANT (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "torsion dystonia 4", "shortest_name_length": 4}
{"curie": "UMLS:C0855081", "names": ["Stage IV Mixed Cellularity Hodgkin Lymphoma", "Hodgkin's disease mixed cellularity stage IV", "Mixed Cellularity Hodgkin's Disease Stage IV", "Stage IV Mixed Cellularity Hodgkin's Disease", "Stage IV Mixed Cellularity Hodgkin's Lymphoma", "Mixed Cellularity Hodgkin's Lymphoma Stage IV", "Stage IV Mixed Cellularity Classical Hodgkin Lymphoma", "Ann Arbor Stage IV Mixed Cellularity Classic Hodgkin Lymphoma", "Ann Arbor Stage IV Mixed Cellularity Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's disease mixed cellularity stage IV", "shortest_name_length": 43}
{"curie": "MONDO:0003514", "names": ["Grade 3 Teratoma", "Immature teratoma", "Malignant Teratoma", "malignant teratoma", "teratoma, malignant", "TERATOMA, MALIGNANT", "Teratoma, malignant, NOS", "Malignant teratoma, anaplastic", "malignant extragonadal teratoma", "malignant Extragonadal teratoma", "Malignant teratoma, undifferentiated", "primary malignant extragonadal teratoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant teratoma", "shortest_name_length": 16}
{"curie": "MONDO:0015379", "names": ["dermoid cyst of neck", "Dermoid cyst of neck", "Cervical dermoid cyst", "cervical dermoid cyst", "Dermoid cyst of the neck", "dermoid cyst of the neck", "Dermoid cyst of neck (disorder)", "dermoid cyst of neck (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical dermoid cyst", "shortest_name_length": 20}
{"curie": "MONDO:0014682", "names": ["NMTC5", "THYROID CANCER, NONMEDULLARY, 5", "thyroid cancer, nonmedullary, 5", "HABP2 thyroid cancer, nonmedullary", "thyroid cancer, nonmedullary, type 5", "thyroid cancer, nonmedullary caused by mutation in HABP2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid cancer, nonmedullary, 5", "shortest_name_length": 5}
{"curie": "UMLS:C4744710", "names": ["Scrotal Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Scrotal Liposarcoma", "shortest_name_length": 19}
{"curie": "MONDO:0020420", "names": ["pulmonary branch stenosis", "peripheral pulmonary stenosis", "Branch Pulmonary Artery Stenosis", "branch pulmonary artery stenosis", "stenosis of pulmonary artery branch", "pulmonary artery stenosis, branch (not PPS)", "Pulmonary Artery Stenosis, Branch (not PPS)", "stenosis of pulmonary artery branch (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary branch stenosis", "shortest_name_length": 25}
{"curie": "MONDO:0005711", "names": ["CDH", "DIH", "HCD", "diaphragmatic hernia", "hernia diaphragmatic", "Hernia;diaphragmatic", "Diaphragmatic Hernia", "DIAPHRAGMATIC HERNIA", "Diaphragmatic hernia", "Hernia, Diaphragmatic", "HERNIA, DIAPHRAGMATIC", "Diaphragmatic Hernias", "hernia; diaphragmatic", "diaphragmatic; hernia", "diaphragmatic hernias", "Diaphragmatic hernias", "Hemidiaphragm Agenesis", "Hernias, Diaphragmatic", "Hemidiaphragm Ageneses", "Diaphragmatic hernia NOS", "agenesis of hemidiaphragm", "Diaphragmatic hernia, NOS", "Agenesis of Hemidiaphragm", "HEMIDIAPHRAGM, AGENESIS OF", "Diaphragm Unilateral Ageneses", "Diaphragm Unilateral Agenesis", "Diaphragmatic hernia (disorder)", "Congenital Diaphragmatic Defect", "Congenital diaphragmatic hernia", "DIAPHRAGMATIC HERNIA CONGENITAL", "Diaphragmatic hernia congenital", "congenital diaphragmatic defect", "congenital diaphragmatic hernia", "Congenital Diaphragmatic Hernia", "diaphragmatic hernia (diagnosis)", "Defect, Congenital Diaphragmatic", "Diaphragmatic hernia, congenital", "DIAPHRAGMATIC DEFECT, CONGENITAL", "Hernia, Congenital Diaphragmatic", "Congenital hernia, diaphragmatic", "DIAPHRAGMATIC HERNIA, CONGENITAL", "Congenital Diaphragmatic Hernias", "unilateral agenesis of diaphragm", "HERNIA, CONGENITAL DIAPHRAGMATIC", "Diaphragmatic Defect, Congenital", "Congenital Diaphragmatic Defects", "Diaphragmatic Hernia, Congenital", "Unilateral Agenesis of Diaphragm", "Diaphragmatic Defects, Congenital", "hernia; diaphragmatic, congenital", "Hernias, Congenital Diaphragmatic", "HERNIA, DIAPHRAGMATIC, CONGENITAL", "Diaphragmatic Hernias, Congenital", "Defects, Congenital Diaphragmatic", "DIAPHRAGM, UNILATERAL AGENESIS OF", "Hernias, Diaphragmatic, Congenital", "hernia; diaphragm defect, congenital", "Congenital diaphragmatic hernia, NOS", "CDH - Congenital diaphragmatic hernia", "diaphragm; defect, congenital with hernia", "Congenital diaphragmatic hernia (disorder)", "defect; diaphragm, congenital, with hernia", "congenital diaphragmatic hernia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital diaphragmatic hernia", "shortest_name_length": 3}
{"curie": "MONDO:0005160", "names": ["TAA", "AAA", "ruptured AAA", "Aortic ectasy", "aortic ectasia", "AORTA DILATION", "Aortic ectasia", "dilation aorta", "aorta aneurysm", "aorta dilation", "AORTA ANEURYSM", "Aortic aneurysm", "Aneurysm aortic", "Aortic dilation", "AORTIC ANEURYSM", "Aortic Aneurysm", "Aortic Dilation", "aneurysm; aorta", "Aneurysm;aortic", "aortic aneurysm", "Aortic Aneurysms", "aortic aneurysms", "Aortic aneurysms", "Aneurysm, Aortic", "aortic dilatation", "dilatation; aorta", "Aortic Dilatation", "Aneurysm of aorta", "aorta; dilatation", "aneurysm of aorta", "Aortic dilatation", "Aneurysms, Aortic", "dilatation of aorta", "Dilatation of aorta", "AA - Aortic aneurysm", "Aortic aneurysm, NOS", "AORTA ANEURYSM RUPTURE", "Aneurysm of aorta, NOS", "AORTIC ANEURYSM RUPTURE", "Aortic aneurysm rupture", "rupture aortic aneurysm", "aortic aneurysm rupture", "ruptured aortic aneurysm", "Ruptured Aortic Aneurysm", "Ruptured aortic aneurysm", "Aneurysm, Ruptured Aortic", "aorta; aneurysm, ruptured", "aortic aneurysm (disease)", "rupture; aortic, aneurysm", "Aortic Aneurysm, Ruptured", "aneurysm; aorta, ruptured", "Ruptured Aortic Aneurysms", "Ruptured Thoracic Aneurysm", "Aneurysms, Ruptured Aortic", "ruptured thoracic aneurysm", "Aortic aneurysm (disorder)", "aortic ectasia (diagnosis)", "Ruptured aneurysm of aorta", "thorax; aneurysm, ruptured", "Aortic Aneurysms, Ruptured", "Thoracic aneurysm, ruptured", "aortic aneurysm (diagnosis)", "Abdominal aneurysm, ruptured", "aneurysm; abdominal, ruptured", "Ruptured aortic aneurysm, NOS", "Dilatation of aorta (disorder)", "Ruptured thoracic aortic aneurysm", "rupture; aneurysm, thoracic aorta", "rupture; thoracic aorta, aneurysm", "ruptured thoracic aortic aneurysm", "Ruptured Abdominal Aortic Aneurysm", "aorta thoracic; aneurysm, ruptured", "Thoracic aortic aneurysm, ruptured", "rupture; abdominal aorta, aneurysm", "thoracic aortic aneurysm, ruptured", "Ruptured abdominal aortic aneurysm", "aneurysm; thoracic aorta, ruptured", "ruptured abdominal aortic aneurysm", "rupture; aneurysm, abdominal aorta", "abdominal aortic aneurysm, ruptured", "Thoracoabdominal aneurysm, ruptured", "Ruptured aortic aneurysm (disorder)", "Abdominal aortic aneurysm, ruptured", "aneurysm; abdominal aorta, ruptured", "ANEURYSM, AORTA, ABDOMINAL, RUPTURED", "aneurysm; thoracoabdominal, ruptured", "Ruptured aneurysm of abdominal aorta", "ruptured aortic aneurysm (diagnosis)", "ruptured aneurysm of abdominal aorta", "aorta abdominalis; aneurysm, ruptured", "thorax; aneurysm, dissecans (ruptured)", "ruptured thoracoabdominal aortic aneurysm", "Thoracoabdominal aortic aneurysm, ruptured", "thoracoabdominal aortic aneurysm, ruptured", "aneurysm; aorta, thoracoabdominal, ruptured", "rupture; aortic, thoracoabdominal, aneurysm", "aorta; thoracoabdominal, aneurysm, ruptured", "ruptured aneurysm of thoracoabdominal aorta", "Thoracic aortic aneurysm which has ruptured", "aorta; aneurysm, thoracoabdominal, ruptured", "rupture; aneurysm, aortic, thoracoabdominal", "thoracic aortic aneurysm which HAS ruptured", "Abdominal aortic aneurysm which has ruptured", "thoracoabdominal; aortic, aneurysm, ruptured", "Ruptured abdominal aortic aneurysm (disorder)", "Aortic aneurysm of unspecified site, ruptured", "ruptured thoracic aortic aneurysm (diagnosis)", "aortic aneurysm of unspecified site, ruptured", "Thoracic aortic aneurysm, ruptured, unspecified", "Abdominal aortic aneurysm, ruptured, unspecified", "ruptured aneurysm of abdominal aorta (diagnosis)", "Thoracoabdominal aortic aneurysm, ruptured (disorder)", "Thoracic aortic aneurysm which has ruptured (disorder)", "ruptured aneurysm of thoracoabdominal aorta (diagnosis)", "Thoracoabdominal aortic aneurysm, ruptured, unspecified", "Bulge in wall of large artery that carries blood away from heart"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic aneurysm", "shortest_name_length": 3}
{"curie": "MONDO:0001401", "names": ["female breast nipple and areola cancer", "malignant tumor of nipple or areola of female breast", "malignant neoplasm of nipple or areola of female breast", "malignant neoplasm of nipple and areola of female breast", "Malignant neoplasm of nipple and areola of female breast", "Malignant neoplasm of nipple and areola of female breast (disorder)", "malignant neoplasm of nipple or areola of female breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "female breast nipple and areola cancer", "shortest_name_length": 38}
{"curie": "UMLS:C0856108", "names": ["Hypercholesterolemia aggravated", "Hypercholesterolaemia aggravated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypercholesterolaemia aggravated", "shortest_name_length": 31}
{"curie": "MONDO:0021633", "names": ["Cerebral Astrocytoma", "cerebral astrocytoma", "Cerebral Astrocytomas", "Astrocytoma, Cerebral", "Astrocytoma of Cerebrum", "astrocytoma of cerebrum", "Astrocytoma of cerebrum", "Astrocytoma of the Cerebrum", "astrocytoma of the cerebrum", "Cerebral Hemispheric Astrocytoma", "cerebral hemispheric astrocytoma", "Astrocytoma of cerebrum (disorder)", "astrocytoma of cerebral hemispheres", "Astrocytoma of cerebrum (diagnosis)", "Astrocytoma of Cerebral Hemispheres", "Astrocytoma of the Cerebral Hemispheres", "astrocytoma of the cerebral hemispheres", "brain tumor malignant astrocytoma cerebrum", "cerebral hemisphere astrocytoma (excluding glioblastoma)", "astrocytoma (excluding glioblastoma) of cerebral hemisphere"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral astrocytoma", "shortest_name_length": 20}
{"curie": "MONDO:0044702", "names": ["DFNX7", "X-linked deafness 7", "deafness, X-linked 7", "DEAFNESS, X-LINKED 7", "deafness, X-linked 7, X-linked recessive", "X-linked external auditory canal atresia-dilated internal auditory canal-facial dysmorphism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked external auditory canal atresia-dilated internal auditory canal-facial dysmorphism syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0100257", "names": ["peroxisomal single enzyme/protein defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisomal single enzyme/protein defect", "shortest_name_length": 40}
{"curie": "MONDO:0005272", "names": ["RA", "RCUD", "MDS-SLD", "Erythrodysplasia", "REFRACTORY ANEMIA", "anemia refractory", "ANEMIA REFRACTORY", "Refractory Anemia", "Anemia refractory", "refractory anemia", "Refractory anemia", "refractory anemias", "Anemia, Refractory", "Refractory anemias", "refractory; anemia", "anemia; refractory", "ANEMIA, REFRACTORY", "Anaemia refractory", "Refractory anaemia", "Refractory Anemias", "refractory anaemia", "Anemias, Refractory", "Aregenerative Anemia", "aregenerative anemia", "Refractory anemia NOS", "Refractory anemia (RA)", "RA - Refractory anemia", "Refractory anaemia NOS", "Refractory anemia, NOS", "Refractory anaemia, NOS", "RA - Refractory anaemia", "Refractory anemia (clinical)", "Refractory anaemia (clinical)", "refractory anemia (diagnosis)", "MDS with single lineage dysplasia", "Refractory anemia without sideroblasts", "Refractory anaemia without sideroblasts", "anemia; refractory, without sideroblasts", "refractory; anemia, without sideroblasts", "Refractory anemia (morphologic abnormality)", "Refractory Cytopenia with Unilineage Dysplasia", "Refractory cytopenia with unilineage dysplasia", "Refractory cytopaenia with unilineage dysplasia", "Myelodysplastic Syndrome with Single Lineage Dysplasia", "myelodysplastic syndrome with single lineage dysplasia", "Myelodysplastic syndrome with single lineage dysplasia", "myelodysplastic syndromes with single lineage dysplasia", "Myelodysplastic syndrome with single lineage dysplasia (disorder)", "myelodysplastic syndromes with single lineage dysplasia (diagnosis)", "Refractory anemia, without ringed sideroblasts, without excess blasts", "Myelodysplastic syndrome with single lineage dysplasia (morphologic abnormality)", "Myelodysplastic syndrome: Refractory anemia, without ringed sideroblasts, without excess blasts", "Myelodysplastic syndrome: refractory anemia, without ringed sideroblasts, without excess blasts", "Myelodysplastic syndrome: Refractory anaemia, without ringed sideroblasts, without excess blasts", "Myelodysplastic syndrome: Refractory anemia, without ringed sideroblasts, without excess blasts (disorder)", "Myelodysplastic syndrome: refractory anemia, without ringed sideroblasts, without excess blasts (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myelodysplastic syndrome with single lineage dysplasia", "shortest_name_length": 2}
{"curie": "MONDO:0011974", "names": ["RP7", "RP 7", "LCA18", "retinitis pigmentosa 7", "Retinitis Pigmentosa 7", "RETINITIS PIGMENTOSA 7", "retinitis pigmentosa type 7", "Leber congenital amaurosis 18", "LEBER CONGENITAL AMAUROSIS 18", "RETINITIS PIGMENTOSA 7, DIGENIC", "Retinitis Pigmentosa 7, Digenic", "retinitis pigmentosa 7, digenic", "leber congenital amaurosis 18, autosomal recessive, autosomal dominant, digenic dominant", "retinitis pigmentosa 7, digenic form, autosomal recessive, autosomal dominant, digenic dominant", "retinitis pigmentosa 7 and digenic form, autosomal recessive, autosomal dominant, digenic dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 7", "shortest_name_length": 3}
{"curie": "MONDO:0035826", "names": ["Symptomatic form of XLMTM in female carriers", "Symptomatic form of XLCNM in female carriers", "Symptomatic form of X-linked myotubular myopathy in female carriers", "symptomatic form of X-linked centronuclear myopathy in female carriers"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "symptomatic form of X-linked centronuclear myopathy in female carriers", "shortest_name_length": 44}
{"curie": "UMLS:C5669922", "names": ["Infant-Type Hemispheric Glioma, ALK-Altered"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infant-Type Hemispheric Glioma, ALK-Altered", "shortest_name_length": 43}
{"curie": "MONDO:0002677", "names": ["classic fibrosarcoma", "Classic Fibrosarcoma", "Classical Fibrosarcoma", "classical fibrosarcoma", "Conventional Fibrosarcoma", "conventional fibrosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "conventional fibrosarcoma", "shortest_name_length": 20}
{"curie": "UMLS:C4722306", "names": ["Metastatic Neuroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Neuroblastoma", "shortest_name_length": 24}
{"curie": "MONDO:0019489", "names": ["diffuse palmoplantar keratoderma - acrocyanosis syndrome", "diffuse palmoplantar hyperkeratosis-acrocyanosis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diffuse palmoplantar keratoderma - acrocyanosis syndrome", "shortest_name_length": 56}
{"curie": "UMLS:C5420222", "names": ["Oral Verruca Vulgaris"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral Verruca Vulgaris", "shortest_name_length": 21}
{"curie": "UMLS:C2936915", "names": ["Deficiency of dextrin", "Amylo-1,6-glucosidase deficiency", "Deficiency of 6-alpha-D-glucosidase", "Deficiency of amylo-1,6-glucosidase", "Deficiency of amylo-1,6-glucosidase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Amylo-1,6-glucosidase deficiency", "shortest_name_length": 21}
{"curie": "MONDO:0016775", "names": ["LP pemphigoides", "Lichen planus pemphigoides", "lichen planus pemphigoides", "Lichen planus pemphigoides (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lichen planus pemphigoides", "shortest_name_length": 15}
{"curie": "UMLS:C0267158", "names": ["Reflux gastritis", "reflux gastritis", "Reflux gastritis (disorder)", "reflux gastritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reflux gastritis", "shortest_name_length": 16}
{"curie": "MONDO:0022089", "names": ["Carnevale hernandez castillo syndrome", "Carnevale Hernandez Castillo syndrome", "Triphalyngeal thumbs and brachyectrodactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carnevale hernandez castillo syndrome", "shortest_name_length": 37}
{"curie": "UMLS:C5447499", "names": ["Advanced Distal Bile Duct Adenocarcinoma", "Advanced Extrahepatic Cholangiocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Distal Bile Duct Adenocarcinoma", "shortest_name_length": 40}
{"curie": "UMLS:C4055192", "names": ["Infection Associated Congenital Nephrotic Syndrome", "Congenital Nephrotic Syndrome - Infection Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Nephrotic Syndrome - Infection Associated", "shortest_name_length": 50}
{"curie": "MONDO:0030533", "names": ["MRT73", "autosomal recessive intellectual developmental disorder 73", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 73", "intellectual developmental disorder, autosomal recessive 73"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder, autosomal recessive 73", "shortest_name_length": 5}
{"curie": "MONDO:0015517", "names": ["cvid", "CVAG", "CVID", "Primary antibody deficiency", "primary antibody deficiency", "Acquired Agammaglobulinemia", "acquired agammaglobulinemia", "acquired; agammaglobulinemia", "Primary dysgammaglobulinemia", "agammaglobulinemia; acquired", "primary hypogammaglobulinemia", "Primary hypogammaglobulinemia", "Acquired dysgammaglobulinemia", "Acquired Hypogammaglobulinemia", "acquired hypogammaglobulinemia", "Acquired hypogammaglobulinemia", "COMMON VARIED IMMUNODEFICIENCY", "Sporadic hypogammaglobulinemia", "sporadic hypogammaglobulinemia", "secondary hypogammaglobulinemia", "Acquired hypogammaglobulinaemia", "Acquired Hypogammaglobulinemias", "Congenital dysgammaglobulinemia", "Secondary Hypogammaglobulinemia", "Hypogammaglobulinemia, Acquired", "Hypogammaglobulinemias, Acquired", "Common Variable Immunodeficiency", "IMMUNODEFICIENCY COMMON VARIABLE", "COMMON VARIABLE IMMUNODEFICIENCY", "common variable immunodeficiency", "common immunodeficiency variable", "Common variable immunodeficiency", "Immunodeficiency common variable", "hypogamma-globulinemia, acquired", "IMMUNODEFICIENCY, COMMON VARIABLE", "common variable immune deficiency", "common variable; immunodeficiency", "Common Variable Immune Deficiency", "immunodeficiency; common variable", "Immunodeficiency, Common Variable", "Common variable agammaglobulinemia", "Common Variable Immunodeficiencies", "common variable agammaglobulinemia", "Variable immunodeficiency syndrome", "Common variable agammaglobulinaemia", "agammaglobulinemia; common variable", "common variable; agammaglobulinemia", "Immunodeficiencies, Common Variable", "Idiopathic immunoglobulin deficiency", "idiopathic immunoglobulin deficiency", "Late onset immunoglobulin deficiency", "Immunoglobulin deficiency, late-onset", "common variable hypogammaglobulinemia", "Common Variable Hypogammaglobulinemia", "Common variable hypogammaglobulinemia", "Acquired primary hypogammaglobulinemia", "Variable Hypogammaglobulinemia, Common", "CVI - Common variable immunodeficiency", "Primary acquired hypogammaglobulinemia", "Common variable hypogammaglobulinaemia", "Hypogammaglobulinemia, Common Variable", "common variable hypogamma-globulinemia", "Common Variable Hypogammaglobulinemias", "Hypogammaglobulinemias, Common Variable", "Variable Hypogammaglobulinemias, Common", "Primary acquired hypogammaglobulinaemia", "Acquired agammaglobulinemia, late onset", "CVID - Common variable immunodeficiency", "Common variable immune deficiency (CVID)", "Common variable immunodeficiency, unspecified", "Common variable agammaglobulinemia (disorder)", "Congenital non-sex-linked hypogammaglobulinemia", "common variable hypogammaglobulinemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "common variable immunodeficiency", "shortest_name_length": 4}
{"curie": "UMLS:C4086161", "names": ["Childhood Immature Teratoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Immature Teratoma", "shortest_name_length": 27}
{"curie": "MONDO:0007087", "names": ["AHC1", "alternating hemiplegia of childhood 1", "ALTERNATING HEMIPLEGIA OF CHILDHOOD 1", "alternating hemiplegia of childhood type 1", "ATP1A2 alternating hemiplegia of childhood", "alternating hemiplegia of childhood caused by mutation in ATP1A2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alternating hemiplegia of childhood 1", "shortest_name_length": 4}
{"curie": "MONDO:0032927", "names": ["TKFCD", "triokinase and FMN cyclase deficiency syndrome", "TRIOKINASE AND FMN CYCLASE DEFICIENCY SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "triokinase and FMN cyclase deficiency syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0017221", "names": ["severe PMD", "connatal PMD", "Pelizaeus-Merzbacher disease type II", "Pelizaeus-Merzbacher disease, connatal form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pelizaeus-Merzbacher disease, connatal form", "shortest_name_length": 10}
{"curie": "UMLS:C5205447", "names": ["HMCSCC", "Hematologic Malignancy-Associated Skin Squamous Cell Carcinoma", "Hematologic Malignancy-Associated Cutaneous Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hematologic Malignancy-Associated Skin Squamous Cell Carcinoma", "shortest_name_length": 6}
{"curie": "MONDO:0008310", "names": ["HGPS", "Progeria", "progeria", "PROGERIA", "Progeria syndrome", "Senilism syndrome", "Hutchinson-Gilford", "Gilford-Hutchinson", "Gilford's syndrome", "progeria (diagnosis)", "Hutchinson-Gilford disease", "Hutchinson-Gilford Disease", "Hutchinson-Gilford Syndrome", "Premature Senility Syndrome", "Hutchinson Gilford Syndrome", "Premature senility syndrome", "Hutchinson Gilford syndrome", "hutchinson-gilford syndrome", "hutchinson gilford syndrome", "premature senility syndrome", "Hutchinson-Gilford syndrome", "Hutchinson-Gilford progeria", "syndrome; premature senility", "premature senility; syndrome", "PROGERIA SYNDROME, CHILDHOOD-ONSET", "progeria syndrome, childhood-onset", "Progeria Syndrome, Childhood-Onset", "HUTCHINSON-GILFORD PROGERIA SYNDROME", "Hutchinson-Gilford Progeria syndrome", "Hutchinson-Gilford progeria syndrome", "Hutchinson Gilford progeria syndrome", "Hutchinson-Gilford Progeria Syndrome", "Hutchinson Gilford Progeria Syndrome", "Progeria Syndrome, Hutchinson-Gilford", "Hutchinson-Gilford Progeria Syndromes", "Progeria Syndromes, Hutchinson-Gilford", "Hutchinson-Gilford syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hutchinson-Gilford progeria syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0023488", "names": ["leukemia radiation", "radiation leukemia", "Radiation-Related Leukemia", "Radiation Induced Leukemia", "radiation induced leukemia", "Radiation-Induced Leukemia", "Leukemia, Radiation-Induced", "Leukemia, Radiation-induced", "Leukemia, Radiation Induced", "Radiation-Induced Leukemias", "Leukemias, Radiation-Induced"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leukemia, Radiation-Induced", "shortest_name_length": 18}
{"curie": "MONDO:0019599", "names": ["primary lipodystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary lipodystrophy", "shortest_name_length": 21}
{"curie": "MONDO:0005452", "names": ["Bulimia", "bulimia", "bulimia nervosa", "Bulimia nervosa", "Bulimia Nervosa", "Nervosa, Bulimia", "hyperorexia nervosa", "BN - Bulimia nervosa", "Bulimia nervosa (disorder)", "bulimia nervosa (diagnosis)", "EATING DISORDER BULIMIA NERVOSA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bulimia nervosa", "shortest_name_length": 7}
{"curie": "UMLS:C5552685", "names": ["Thrombotic Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thrombotic Disorder", "shortest_name_length": 19}
{"curie": "UMLS:C0403452", "names": ["Acute cortical necrosis", "Acute Cortical Necrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Cortical Necrosis", "shortest_name_length": 23}
{"curie": "MONDO:0003831", "names": ["type 2 renal papillary adenoma", "Type 2 Renal Papillary Adenoma", "Type 2 Papillary Adenoma of the Kidney", "type 2 papillary adenoma of the kidney"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type 2 papillary adenoma of the kidney", "shortest_name_length": 30}
{"curie": "MONDO:0005982", "names": ["Tinea", "TINEA", "tinea", "tineas", "Tineas", "ringworm", "Ringworm", "Tinea NOS", "ringworms", "Tinea, NOS", "Ringworm NOS", "Ringworm, NOS", "TINEA INFECTION", "tinea infection", "Dermatophytoses", "Tinea Infection", "infection tinea", "Tinea infection", "Dermatophytosis", "Tinea Infections", "tinea infections", "Tinea infections", "Microsporic tinea", "tinea; microsporic", "Tinea infection NOS", "Microsporic tinea NOS", "Microsporic tinea, NOS", "Tinea infectious disease", "Tinea disease or disorder", "Tinea caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tinea infection", "shortest_name_length": 5}
{"curie": "MONDO:0010173", "names": ["CAUV", "MRKH", "MRK anomaly", "Mrk anomaly", "MRK ANOMALY", "RKH syndrome", "MRKH ANOMALY", "MRKH anomaly", "MRKH syndrome", "MRKH Syndrome", "MRKH SYNDROME", "Müllerian agenesis", "Rokitansky sequence", "Rokitansky syndrome", "MRKH syndrome type 1", "Mullerian dysgenesis", "urogenital adysplasia", "Urogenital adysplasia", "UROGENITAL ADYSPLASIA", "genital renal ear syndrome", "Mullerian aplasia/dysgenesis", "MULLERIAN APLASIA/DYSGENESIS", "Mullerian Aplasia-Dysgenesis", "Rokitansky sequence (disorder)", "Mayer-Rokitansky-Kuster syndrome", "urogenital adysplasia (diagnosis)", "Rokitansky Kuster Hauser syndrome", "Von Mayer-Rokitansky-Kuster Anomaly", "VON MAYER-ROKITANSKY-KUSTER ANOMALY", "Von Mayer Rokitansky Kuster anomaly", "Von Mayer-Rokitansky-Kuster anomaly", "CONGENITAL ABSENCE OF UTERUS AND VAGINA", "Mayer Rokitansky Kuster Hauser syndrome", "MAYER-ROKITANSKY-KUSTER-HAUSER SYNDROME", "Mayer-Rokitansky-KUSTER-Hauser syndrome", "Congenital absence of uterus and vagina", "Mayer-Rokitansky-Kuster-Hauser Syndrome", "congenital absence of uterus and vagina", "Mayer-Rokitansky-Kuster-Hauser syndrome", "Mayer-Rokitansky-Küster-Hauser syndrome", "Mayer-Rokitansky-Kuster-Hauser syndrome type 1", "Mayer-Rokitansky-Küster-Hauser syndrome type 1", "Mayer-Rokitansky-Kuster-Hauser syndrome (MRKH)", "congenital absence of the uterus and vagina (CAUV)", "Uterus bipartitus solidus rudimentarius cum vagina solida", "uterus Bipartitus solidus Rudimentarius cum vagina Solida", "UTERUS BIPARTITUS SOLIDUS RUDIMENTARIUS CUM VAGINA SOLIDA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mayer-Rokitansky-Kuster-Hauser syndrome type 1", "shortest_name_length": 4}
{"curie": "UMLS:C1336187", "names": ["Stage IIB Melanoma", "Stage IIB Melanoma of Skin", "Stage IIB Melanoma of the Skin", "Stage IIB Skin Melanoma AJCC v6", "Stage IIB Skin Melanoma AJCC v7", "Stage IIB Cutaneous (Skin) Melanoma", "Stage IIB Cutaneous Melanoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Cutaneous Melanoma AJCC v6 and v7", "shortest_name_length": 18}
{"curie": "UMLS:C4526725", "names": ["Stage IV", "Stage IV Lung Cancer", "Stage IV Lung Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Lung Cancer AJCC v8", "shortest_name_length": 8}
{"curie": "MONDO:0009883", "names": ["antiplasmin defiency", "Antiplasmin Deficiency", "ANTIPLASMIN DEFICIENCY", "antiplasmin deficiency", "PLASMIN INHIBITOR DEFICIENCY", "Plasmin Inhibitor Deficiency", "plasmin inhibitor deficiency", "antiplasmin deficiency, congenital", "Antiplasmin deficiency, congenital", "anti-plasmin deficiency, congenital", "Anti-plasmin deficiency, congenital", "alpha-2-plasmin inhibitor deficiency", "ALPHA-2-PLASMIN INHIBITOR DEFICIENCY", "Alpha-2-plasmin inhibitor deficiency", "Congenital alpha2-antiplasmin deficiency", "congenital alpha2-antiplasmin deficiency", "Congenital alpha-2-antiplasmin deficiency", "Congenital alpha-2-antiplasmin deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alpha-2-plasmin inhibitor deficiency", "shortest_name_length": 20}
{"curie": "MONDO:0015532", "names": ["Nodular non-X histiocytosis", "Generalized eruptive histiocytoma", "Generalised eruptive histiocytoma", "generalized eruptive histiocytoma", "Generalized eruptive histiocytosis", "generalized eruptive histiocytosis", "Histiocytosis, generalized eruptive", "Generalized eruptive histiocytoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "generalized eruptive histiocytosis", "shortest_name_length": 27}
{"curie": "MONDO:0010032", "names": ["Sjogren-Larsson-like syndrome", "Sjogren-Larsson-like ichthyosis without CNS or eye involvement", "SJOGREN-LARSSON-LIKE ICHTHYOSIS WITHOUT CNS OR EYE INVOLVEMENT", "ichthyosis, Sjogren-Larsson-like, without CNS or eye involvement", "Ichthyosis, Sjogren-Larsson-Like, Without CNS Or Eye Involvement", "ICHTHYOSIS, SJOGREN-LARSSON-LIKE, WITHOUT CNS OR EYE INVOLVEMENT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sjogren-Larsson-like ichthyosis without CNS or eye involvement", "shortest_name_length": 29}
{"curie": "MONDO:0007884", "names": ["LEG ULCERS, FAMILIAL, OF JUVENILE ONSET", "Leg Ulcers, Familial, of Juvenile Onset", "leg ulcers, familial, of juvenile onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leg ulcers, familial, of juvenile onset", "shortest_name_length": 39}
{"curie": "UMLS:C0677930", "names": ["primary", "Primary", "Primary Tumor", "primary tumor", "primary tumors", "Primary Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Neoplasm", "shortest_name_length": 7}
{"curie": "MONDO:0005904", "names": ["PERICARDITIS", "Pericarditis", "pericarditis", "Pericarditis NOS", "Pericarditis, NOS", "pericarditis (disease)", "Pericarditis (disorder)", "pericarditis (diagnosis)", "pericardium inflammation", "inflammation; pericardium", "pericardium; inflammation", "inflammation of pericardium", "Swelling or irritation of membrane around heart", "an inflammation of the membrane surrounding the heart"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pericarditis", "shortest_name_length": 12}
{"curie": "UMLS:C0424605", "names": ["development delay", "developmental delay", "DEVELOPMENTAL DELAY", "Delayed Development", "Developmental delay", "Delayed development", "Developmental Delay", "delayed development", "delays developmental", "Developmental delays", "disturbance; learning", "Developmental delay NOS", "development; retardation", "DEVELOPMENTAL RETARDATION", "child developmental delay", "developmental retardation", "retardation; developmental", "Developmental delay (disorder)", "Delayed developmental milestones", "Unspecified delay in development"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Developmental delay", "shortest_name_length": 17}
{"curie": "UMLS:C5554874", "names": ["Dedifferentiated Leiomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dedifferentiated Leiomyosarcoma", "shortest_name_length": 31}
{"curie": "MONDO:0021167", "names": ["Myositis", "MYOSITIS", "myositis", "Myositides", "myositis nos", "Myositis, NOS", "myositis disease", "Myositis (disorder)", "muscle inflammation", "Muscle inflammation", "inflammation; muscle", "Unspecified myositis", "muscle; inflammation", "myositis (diagnosis)", "Inflammatory Myopathy", "MYOSITIS INFLAMMATORY", "Myositis, unspecified", "Inflammatory myopathy", "inflammatory myopathy", "Inflammation;muscle(s)", "Myopathy, Inflammatory", "myopathy; inflammatory", "inflammatory; myopathy", "Inflammatory Myopathies", "inflammatory myopathies", "Myopathies, Inflammatory", "Inflammatory myopathy NOS", "muscle tissue inflammation", "inflammatory muscle disease", "Inflammatory Muscle Disease", "Inflammatory Muscle Diseases", "inflammatory muscle diseases", "Muscle Disease, Inflammatory", "Muscle Diseases, Inflammatory", "inflammation of the muscle(s)", "inflammation of muscle tissue", "muscle; disease, inflammatory", "Inflammatory disorder of muscle", "inflammatory disorder of muscle", "inflammatory myopathy (diagnosis)", "inflammation of the skeletal muscle", "inflammatory disorder of muscle (disorder)", "disease (or disorder); muscle, inflammatory"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myositis disease", "shortest_name_length": 8}
{"curie": "MONDO:0800187", "names": ["IIAE2", "IMD83", "HERPES SIMPLEX ENCEPHALITIS, SUSCEPTIBILITY TO, 2", "IMMUNODEFICIENCY 83, SUSCEPTIBILITY TO VIRAL INFECTIONS", "immunodeficiency 83, susceptibility to viral infections", "PNEUMONITIS, INFECTION (VIRAL)-INDUCED, SUSCEPTIBILITY TO", "ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 83, susceptibility to viral infections", "shortest_name_length": 5}
{"curie": "MONDO:0014677", "names": ["ACHM7", "ACHROMATOPSIA 7", "achromatopsia 7", "ATF6 achromatopsia", "achromatopsia type 7", "achromatopsia caused by mutation in ATF6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "achromatopsia 7", "shortest_name_length": 5}
{"curie": "MONDO:0009162", "names": ["EVC", "Ellis-van Creveld", "mesodermic dysplasia", "Mesodermic dysplasia", "six-fingered dwarfism", "Mesoectodermal dysplasia", "mesoectodermal dysplasia", "Mesoectodermal Dysplasia", "MESOECTODERMAL DYSPLASIA", "Dysplasia, Mesoectodermal", "Mesoectodermal Dysplasias", "creveld ellis-van syndrome", "ELLIS VAN CREVELD SYNDROME", "Ellis-van Creveld syndrome", "Ellis-VAN Creveld syndrome", "Ellis Van Creveld syndrome", "ELLIS-VAN CREVELD SYNDROME", "ellis van creveld syndrome", "Ellis-Van Creveld syndrome", "Ellis Van Creveld Syndrome", "ellis-van creveld syndrome", "Ellis-Van Creveld Syndrome", "Ellis-Van Creveld Dysplasia", "Chondroectodermal dysplasia", "Chondroectodermal Dysplasia", "CHONDROECTODERMAL DYSPLASIA", "chondroectodermal dysplasia", "Ellis Van Creveld Dysplasia", "Syndrome, Ellis-Van Creveld", "chondroectodermal; dysplasia", "Dysplasia, Chondroectodermal", "Chondroectodermal Dysplasias", "dysplasia; chondroectodermal", "Dysplasia, Ellis-Van Creveld", "chondrodysplasia ectodermica", "Ellis-van Creveld (EvC) syndrome", "EVC - Ellis-van Creveld syndrome", "chondroectodermal dysplasia (CED)", "Chondroectodermal dysplasia syndrome", "polydactyly-chondrodystrophy syndrome", "Chondroectodermal dysplasia (disorder)", "Ellis-van Creveld syndrome (diagnosis)", "dwarfism-polydactyly-dysplastic nails syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ellis-van Creveld syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0700079", "names": ["HR-positive HER2-negative breast cancer", "hormone receptor-positive breast cancer", "Hormone receptor positive HER2 negative breast cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hormone receptor-positive breast cancer", "shortest_name_length": 39}
{"curie": "UMLS:C4688586", "names": ["Stage IV Malignant Thymic Germ Cell Tumor", "Stage IV Malignant Mediastinal Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Malignant Mediastinal Germ Cell Tumor", "shortest_name_length": 41}
{"curie": "UMLS:C1323189", "names": ["Infected dermatitis", "Dermatitis infected", "Impetigenized dermatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infected dermatitis", "shortest_name_length": 19}
{"curie": "MONDO:0024284", "names": ["sebaceous gland demodicidosis", "demodicidosis of sebaceous gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "demodicidosis of sebaceous gland", "shortest_name_length": 29}
{"curie": "MONDO:0013366", "names": ["SCDO4", "spondylocostal dysostosis 4", "autosomal recessive spondylocostal dysostosis 4", "SPONDYLOCOSTAL DYSOSTOSIS 4, AUTOSOMAL RECESSIVE", "spondylocostal dysostosis 4, autosomal recessive", "HES7 autosomal recessive spondylocostal dysostosis", "Hes7 autosomal recessive spondylocostal dysostosis", "autosomal recessive spondylocostal dysostosis caused by mutation in HES7", "autosomal recessive spondylocostal dysostosis caused by mutation in Hes7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondylocostal dysostosis 4, autosomal recessive", "shortest_name_length": 5}
{"curie": "UMLS:C4289588", "names": ["Endometrial Large Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endometrial Large Cell Neuroendocrine Carcinoma", "shortest_name_length": 47}
{"curie": "UMLS:C1262098", "names": ["hyperthyroidism congenital", "congenital hyperthyroidism", "Congenital hyperthyroidism", "Congenital Hyperthyroidism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital hyperthyroidism", "shortest_name_length": 26}
{"curie": "MONDO:0013385", "names": ["TCS2", "Treacher Collins syndrome 2", "TREACHER COLLINS SYNDROME 2", "TREACHER COLLINS syndrome 2", "Treacher Collins syndrome type 2", "POLR1D Treacher-Collins syndrome", "Treacher-Collins syndrome caused by mutation in POLR1D"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Treacher Collins syndrome 2", "shortest_name_length": 4}
{"curie": "MONDO:0004619", "names": ["measle", "MEASLE", "rubeola", "Measles", "MEASLES", "measles", "RUBEOLA", "Rubeola", "Morbilli", "RUBEOLLA", "morbilli", "Measles NOS", "Measles disease", "Rubeola Infection", "rubeola infection", "Measles (disorder)", "measles (diagnosis)", "Rubeola virus infection", "Measles morbillivirus infectious disease", "Measles morbillivirus disease or disorder", "Measles morbillivirus caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "measles", "shortest_name_length": 6}
{"curie": "UMLS:C1335034", "names": ["Non-Neoplastic Pleural Disease", "Non-Neoplastic Pleural Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Pleural Disorder", "shortest_name_length": 30}
{"curie": "MONDO:0015102", "names": ["non-secreting chemodectoma", "non-functioning chemodectoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-secreting chemodectoma", "shortest_name_length": 26}
{"curie": "UMLS:C1516056", "names": ["Astler-Coller A Colon Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Astler-Coller A Colon Carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0011013", "names": ["HYPOC1", "hypocalcemia, familial", "hypercalciuric hypocalcemia", "hypocalcemia, autosomal dominant", "autosomal dominant hypocalcemia 1", "hypocalcemia, autosomal dominant 1", "CASR autosomal dominant hypocalcemia", "autosomal dominant hypocalcemia type 1", "hypocalcemia, autosomal dominant type 1", "hypocalcemia, autosomal dominant, with Bartter syndrome", "hypocalcemia, autosomal dominant 1, with Bartter syndrome", "HYPOCALCEMIA, AUTOSOMAL DOMINANT 1, WITH BARTTER SYNDROME", "autosomal dominant hypocalcemia caused by mutation in CASR"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant hypocalcemia 1", "shortest_name_length": 6}
{"curie": "UMLS:C0752155", "names": ["CNS Vascular Malformation", "CNS Vascular Malformations", "Vascular Malformation, CNS", "Malformation, CNS Vascular", "Malformations, CNS Vascular", "Vascular Malformations, CNS", "Vascular Malformation of CNS", "Vascular Malformation of the CNS", "Central Nervous System Vascular Anomalies", "Vascular Anomalies, Central Nervous System", "Vascular malformation of the nervous system", "Central Nervous System Vascular Malformation", "Central Nervous System Vascular Malformations", "Vascular Malformations, Central Nervous System", "Vascular Malformations of Central Nervous System", "Vascular Malformations of the Central Nervous System", "Vascular malformation of the nervous system (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Vascular Malformations", "shortest_name_length": 25}
{"curie": "UMLS:C4553669", "names": ["Stage IIIB Primary Peritoneal Cancer", "Stage IIIB Primary Peritoneal Cancer AJCC v8", "Stage IIIB Primary Peritoneal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Primary Peritoneal Cancer AJCC v8", "shortest_name_length": 36}
{"curie": "MONDO:0016049", "names": ["congenital myopathy, Paradas type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myopathy, Paradas type", "shortest_name_length": 33}
{"curie": "MONDO:0009673", "names": ["SMA2", "sma2", "Sma 2", "SMA-II", "SMA II", "SMA type 2", "SMA type II", "Dubowitz disease", "spinal muscular atrophy-2", "spinal muscular atrophy 2", "Spinal Muscular Atrophy Type 2", "spinal muscular atrophy type 2", "Spinal muscular atrophy type II", "Spinal Muscular Atrophy Type II", "chronic spinal muscular atrophy", "Type II Spinal Muscular Atrophy", "spinal muscular atrophy type ii", "spinal muscular atrophy, type 2", "spinal muscular atrophy type II", "spinal muscular atrophy, type II", "SPINAL MUSCULAR ATROPHY, TYPE II", "Spinal muscular atrophy, type II", "Spinal Muscular Atrophy, Type II", "Muscular Atrophy, Spinal, Type II", "intermediate spinal muscular atrophy", "Intermediate spinal muscular atrophy", "Late infantile spinal muscular atrophy", "proximal spinal muscular atrophy type 2", "Proximal spinal muscular atrophy type 2", "chronic infantile spinal muscular atrophy", "muscular atrophy, spinal, intermediate type", "Muscular Atrophy, Spinal, Intermediate Type", "MUSCULAR ATROPHY, SPINAL, INTERMEDIATE TYPE", "Spinal muscular atrophy, type II (disorder)", "muscular atrophy, spinal, Intermediate type", "muscle; atrophy, spinal, of childhood, type II", "atrophy; muscle, spinal, of childhood, type II", "MUSCULAR ATROPHY, SPINAL, INFANTILE CHRONIC FORM", "muscular atrophy, spinal, infantile chronic form", "Muscular atrophy, spinal, infantile chronic form", "Muscular Atrophy, Spinal, Infantile Chronic Form", "[OBSOLETE] Muscular atrophy, spinal, infantile chronic form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal muscular atrophy, type II", "shortest_name_length": 4}
{"curie": "UMLS:C5419763", "names": ["Recurrent Salivary Gland Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Salivary Gland Squamous Cell Carcinoma", "shortest_name_length": 48}
{"curie": "MONDO:0009677", "names": ["DMDA", "Dmda", "DMDA1", "LGMDR5", "SCARMD", "LGMD2C", "LGMD type 2C", "MAGHREBIAN MYOPATHY", "Maghrebian myopathy", "Gamma-sarcoglycanopathy", "gamma-sarcoglycanopathy", "Gamma sarcoglycanopathy", "ADHALIN DEFICIENCY, SECONDARY", "Adhalin deficiency, secondary", "deficiency of sarcoglycan gamma", "sarcoglycan, gamma, deficiency of", "MUSCULAR DYSTROPHY, DUCHENNE-LIKE", "muscular dystrophy, Duchenne-like", "SARCOGLYCAN, GAMMA, DEFICIENCY OF", "Gamma-sarcoglycan-related LGMD R5", "Muscular dystrophy, Duchenne-like", "Limb girdle muscular dystrophy type 2C", "Limb-girdle muscular dystrophy type 2C", "Limb-girdle muscular dystrophy, type 2C", "limb-girdle muscular dystrophy, type 2C", "Muscular Dystrophy, Limb-Girdle, Type 2C", "muscular dystrophy, limb-girdle, type 2C", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2C", "LGMD due to gamma-sarcoglycan deficiency", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 5", "muscular dystrophy, limb-girdle, autosomal recessive 5", "SGCG autosomal recessive limb-girdle muscular dystrophy", "Autosomal recessive limb-girdle muscular dystrophy type 2C", "autosomal recessive limb-girdle muscular dystrophy type 2C", "Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5", "autosomal recessive Duchenne-like muscular dystrophy type 1", "Duchenne-like muscular dystrophy, autosomal recessive, type 1", "DUCHENNE-LIKE MUSCULAR DYSTROPHY, AUTOSOMAL RECESSIVE, TYPE 1", "Limb-girdle muscular dystrophy with gamma-sarcoglycan deficiency", "limb-girdle muscular dystrophy with gamma-sarcoglycan deficiency", "Limb-girdle muscular dystrophy due to gamma-sarcoglycan deficiency", "limb-girdle muscular dystrophy due to gamma-sarcoglycan deficiency", "severe childhood autosomal recessive muscular dystrophy North African type", "severe childhood autosomal recessive muscular dystrophy, North African type", "Severe childhood autosomal recessive muscular dystrophy, North African type", "SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, NORTH AFRICAN TYPE", "autosomal recessive limb-girdle muscular dystrophy caused by mutation in SGCG", "Severe autosomal recessive muscular dystrophy of childhood - North African type", "Severe autosomal recessive muscular dystrophy of childhood - North African type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive limb-girdle muscular dystrophy type 2C", "shortest_name_length": 4}
{"curie": "UMLS:C1290870", "names": ["Axillary Disease", "Axillary Disorder", "disorder of axilla", "Disorder of axilla", "Disorder of axilla (disorder)", "disorder of axilla (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disorder of axilla", "shortest_name_length": 16}
{"curie": "MONDO:0035437", "names": ["CAIN", "CEBPE-associated autoinflammation-immunodeficiency-neutrophil dysfunction syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CEBPE-associated autoinflammation-immunodeficiency-neutrophil dysfunction syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0009498", "names": ["lethal Kniest-like dysplasia", "Kniest like dysplasia lethal", "Lethal Kniest-like dysplasia", "KNIEST-LIKE DYSPLASIA, LETHAL", "Kniest-Like Dysplasia, Lethal", "Kniest-like dysplasia, lethal", "Arthrosis, flat face, hypotonia, short neck and macrocephaly", "arthrosis, flat face, hypotonia, short neck and macrocephaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal Kniest-like dysplasia", "shortest_name_length": 28}
{"curie": "UMLS:C0751381", "names": ["Foley-Denny-Brown Syndrome", "Foley Denny Brown Syndrome", "Syndrome, Foley-Denny-Brown", "Cramp-fasciculation syndrome", "cramp fasciculation syndrome", "cramp-fasciculation syndrome", "Cramp Fasciculation Syndrome", "Cramp-Fasciculation Syndrome", "Syndrome, Cramp-Fasciculation", "Cramp-Fasciculation Syndromes", "Syndromes, Cramp-Fasciculation", "cramping fasciculation syndrome", "Syndrome of Foley and Denny-Brown", "Benign fasciculation cramp syndrome", "Benign fasciculation-cramp syndrome", "Benign Fasciculation-Cramp Syndrome", "Fasciculation Cramp Syndrome, Benign", "Benign Fasciculation-Cramp Syndromes", "Fasciculation-Cramp Syndrome, Benign", "Fasciculation-Cramp Syndromes, Benign", "Benign fasciculation-cramp syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Foley-Denny-Brown Syndrome", "shortest_name_length": 26}
{"curie": "MONDO:0022965", "names": ["DIG", "Desmoplastic Infantile Astrocytoma", "desmoplastic infantile ganglioglioma", "Desmoplastic infantile ganglioglioma", "Desmoplastic Infantile Ganglioglioma", "desmoplastic infantile ganglioglioma / desmoplastic infantile astrocytoma", "desmoplastic infantile ganglioglioma and desmoplastic infantile astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "desmoplastic infantile ganglioglioma", "shortest_name_length": 3}
{"curie": "MONDO:0019569", "names": ["CSA", "Cockayne syndrome A", "COCKAYNE SYNDROME A", "ERCC8 Cockayne syndrome", "Cockayne syndrome type A", "Cockayne Syndrome Type A", "Cockayne syndrome type 1", "Cockayne syndrome type a", "Type I Cockayne Syndrome", "Type A Cockayne Syndrome", "Cockayne syndrome type I", "Cockayne syndrome, type A", "Group A Cockayne Syndrome", "Cockayne Syndrome, Type I", "Cockayne Syndrome, Type A", "Cockayne Syndrome, Group A", "Cockayne syndrome classical", "Classical Cockayne syndrome", "Cockayne syndrome classic form", "Cockayne syndrome type 1 (disorder)", "Cockayne syndrome type A (diagnosis)", "Cockayne syndrome caused by mutation in ERCC8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cockayne syndrome type 1", "shortest_name_length": 3}
{"curie": "MONDO:0014488", "names": ["T2D5", "NIDDM5", "TYPE 2 DIABETES 5", "TBC1D4 type 2 diabetes mellitus", "DIABETES MELLITUS, NONINSULIN-DEPENDENT, 5", "diabetes mellitus, noninsulin-dependent, 5", "diabetes mellitus, noninsulin-dependent, type 5", "type 2 diabetes mellitus caused by mutation in TBC1D4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diabetes mellitus, noninsulin-dependent, 5", "shortest_name_length": 4}
{"curie": "UMLS:C5237415", "names": ["Locally Recurrent Skin Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Recurrent Skin Squamous Cell Carcinoma", "shortest_name_length": 46}
{"curie": "UMLS:C0854145", "names": ["Feeding disorder", "feeding disorder", "Feeding Disorder", "disorder; feeding", "feeding; disorder", "Disorder, Feeding", "Feeding Disorders", "disorders feeding", "Disorders, Feeding", "Feeding disorder NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Feeding Disorders", "shortest_name_length": 16}
{"curie": "UMLS:C1709286", "names": ["Null Cell Adenoma", "Null Cell PitNET/Adenoma", "Hormone Immunonegative Adenoma", "Null Cell Pituitary Neuroendocrine Tumor", "Transcription Factor-Immunonegative Adenoma", "Hormone Immunonegative Pituitary Gland Adenoma", "Null Cell Pituitary Neuroendocrine Tumor/Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Null Cell Pituitary Neuroendocrine Tumor", "shortest_name_length": 17}
{"curie": "MONDO:0019514", "names": ["hepatic Vod", "veno-occlusive disease", "venoocclusive liver disease", "Venoocclusive liver disease", "VENOOCCLUSIVE LIVER DISEASE", "liver veno-occlusive disease", "Liver Veno-Occlusive Disease", "disease liver veno-occlusive", "Hepatic Veno Occlusive Disease", "Hepatic Veno-Occlusive Disease", "hepatic veno-occlusive disease", "Hepatic veno-occlusive disease", "veno-occlusive disease hepatic", "sinusoidal obstruction syndrome", "Hepatic Veno-Occlusive Diseases", "Sinusoidal Obstruction Syndrome", "Disease, Hepatic Veno-Occlusive", "Veno Occlusive Disease, Hepatic", "Veno-Occlusive Disease, Hepatic", "Sinusoidal obstruction syndrome", "Syndrome, Sinusoidal Obstruction", "Venoocclusive syndrome of the liver", "Veno-occlusive disease of the liver", "Hepatic sinusoidal obstruction syndrome", "hepatic veno-occlusive disease (diagnosis)", "Veno-occlusive disease of the liver (disorder)", "disease (or disorder); liver, veno-occlusive [VOD]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatic veno-occlusive disease", "shortest_name_length": 11}
{"curie": "MONDO:0002125", "names": ["SE", "GCSE", "Grand mal status", "epilepsy; status", "grand mal status", "status; epileptic", "Prolonged seizure", "epilepticus status", "Prolonged seizures", "Status Epilepticus", "STATUS EPILEPTICUS", "Status epilepticus", "status epilepticus", "epilepticus; status", "status; epilepticus", "Status epilepticus NOS", "Status epilepticus (disorder)", "Generalized Status Epilepticus", "Status epilepticus (diagnosis)", "Status Epilepticus, Generalized", "Status epilepticus, unspecified", "Repeated seizure without recovery", "seizure disorder status epilepticus", "generalized convulsive status epilepticus", "Repeated seizures without recovery between them"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "status epilepticus", "shortest_name_length": 2}
{"curie": "UMLS:C4683549", "names": ["Stage IV Adrenal Gland Pheochromocytoma and Sympathetic Paraganglioma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Adrenal Gland Pheochromocytoma and Sympathetic Paraganglioma AJCC v8", "shortest_name_length": 77}
{"curie": "UMLS:C0085232", "names": ["zenker diverticula", "Zenker Diverticula", "zenkers diverticula", "Zenker Diverticulum", "Zenkers Diverticula", "diverticulum zenker", "Zenker diverticulum", "zenker diverticulum", "Zenker; diverticulum", "zenkers diverticulum", "Zenker's Diverticula", "Zenkers Diverticulum", "zenker's diverticula", "Diverticulum, Zenker", "diverticulum; Zenker", "Zenker's diverticulum", "Zenker's Diverticulum", "zenker's diverticulum", "Diverticula, Zenker's", "diverticulum zenker's", "Diverticulum, Zenker's", "Pharyngeal Diverticula", "Diverticula, Pharyngeal", "pharyngeal diverticulum", "Pharyngeal Diverticulum", "Diverticulum, Pharyngeal", "hypopharyngeal diverticulum", "Hypopharyngeal diverticulum", "Pharyngoesophageal Diverticula", "Pharyngo-Esophageal Diverticula", "Esophagopharyngeal Diverticulum", "Esophago-Pharyngeal Diverticula", "Esophago Pharyngeal Diverticula", "pharyngoesophageal diverticulum", "Pharyngoesophageal diverticulum", "Pharyngo Esophageal Diverticula", "Pharyngoesophageal Diverticulum", "Diverticula, Pharyngoesophageal", "Pharyngo-Esophageal Diverticulum", "Diverticula, Pharyngo-Esophageal", "pharyngoesophageal; diverticulum", "Diverticula, Esophago-Pharyngeal", "Esophago-Pharyngeal Diverticulum", "Diverticulum, Pharyngoesophageal", "Esophago Pharyngeal Diverticulum", "Esophagopharyngeal Diverticulums", "Diverticulum, Esophagopharyngeal", "diverticulum; pharyngoesophageal", "Pharyngo Esophageal Diverticulum", "Pharyngo-esophageal diverticulum", "Pharyngo-oesophageal diverticulum", "Diverticulum, Esophago-Pharyngeal", "Diverticulums, Esophagopharyngeal", "Diverticulum, Pharyngo-Esophageal", "Zenker's diverticulum (diagnosis)", "Zenker's hypopharyngeal diverticulum", "Pharyngoesophageal Pulsion Diverticula", "Diverticula, Pharyngoesophageal Pulsion", "Pulsion Diverticula, Pharyngoesophageal", "Pharyngoesophageal Pulsion Diverticulum", "Diverticulum, Pharyngoesophageal Pulsion", "Acquired pharyngoesophageal diverticulum", "Pulsion Diverticulum, Pharyngoesophageal", "Acquired pharyngo-oesophageal diverticulum", "Pharyngoesophageal diverticulum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Zenker Diverticulum", "shortest_name_length": 18}
{"curie": "MONDO:0007911", "names": ["Beta-lipoprotein, Double", "BETA-LIPOPROTEIN, DOUBLE", "LIPOPROTEIN, VARIANT OF BETA", "lipoprotein, variant of beta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lipoprotein, variant of beta", "shortest_name_length": 24}
{"curie": "UMLS:C0585186", "names": ["Allergy;skin", "allergy skin", "Skin allergy", "skin allergy", "allergies skin", "Cutaneous allergy", "Allergic skin rash", "allergic skin rash", "skin rash allergic", "skin hypersensitivity", "Skin hypersensitivity", "allergic skin disorder", "Allergic Skin Disorders", "Allergic disorder of skin", "Cutaneous hypersensitivity", "cutaneous hypersensitivity", "hypersensitivity cutaneous", "Hypersensitivity, cutaneous", "allergic skin disorder (diagnosis)", "nature of allergic reaction - rash", "Allergic disorder of skin (disorder)", "Cutaneous hypersensitivity (disorder)", "nature of allergic reaction - rash (history)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Allergic disorder of skin", "shortest_name_length": 12}
{"curie": "MONDO:0021292", "names": ["Stage 0 Gastric Body Carcinoma", "Gastric Body Carcinoma In Situ", "stage 0 gastric body carcinoma", "gastric body carcinoma in situ", "body of stomach in situ carcinoma", "carcinoma in situ of gastric body", "stage 0 body of stomach carcinoma", "Carcinoma in situ of Gastric Body", "body of stomach carcinoma in situ", "Carcinoma in situ of gastric body", "Cancer in situ of body of stomach", "Carcinoma in situ of body of stomach", "Carcinoma in situ of Body of Stomach", "carcinoma in situ of body of stomach", "Carcinoma in situ of the Gastric Body", "carcinoma in situ of the gastric body", "Carcinoma in situ of the Body of the Stomach", "carcinoma in situ of the body of the stomach", "Gastric Body Carcinoma In Situ AJCC v6 and v7", "gastric body carcinoma in situ aJCC v6 and v7", "Carcinoma in situ of body of stomach (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma in situ of gastric body", "shortest_name_length": 30}
{"curie": "MONDO:0000507", "names": ["IBMPFD", "Pagetoid Neuroskeletal Syndrome", "PAGETOID NEUROSKELETAL SYNDROME", "Pagetoid neuroskeletal syndrome", "pagetoid neuroskeletal syndrome", "Pagetoid Amyotrophic Lateral Sclerosis", "Pagetoid amyotrophic lateral sclerosis", "PAGETOID AMYOTROPHIC LATERAL SCLEROSIS", "pagetoid amyotrophic lateral sclerosis", "limb-girdle muscular dystrophy with Paget disease of bone", "Muscular dystrophy limb-girdle with Paget disease of bone", "Limb-girdle muscular dystrophy with Paget disease of bone", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, WITH PAGET DISEASE OF BONE", "Muscular Dystrophy, Limb-Girdle, With Paget Disease Of Bone", "Lower Motor Neuron Degeneration With Paget-Like Bone Disease", "LOWER MOTOR NEURON DEGENERATION WITH PAGET-LIKE BONE DISEASE", "Lower motor neuron degeneration with Paget-like bone disease", "inclusion body myopathy/Paget disease/frontotemporal dementia", "inclusion body myopathy with Paget disease of bone and frontotemporal dementia", "Inclusion body myopathy with Paget disease of bone and frontotemporal dementia", "inclusion body myopathy with Paget's disease of bone and frontotemporal dementia", "Inclusion Body Myopathy with Paget Disease of Bone and-or Frontotemporal Dementia", "inclusion body myopathy with early-onset Paget disease and frontotemporal dementia", "Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia", "Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia", "INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE AND FRONTOTEMPORAL DEMENTIA", "IBMPFD - Inclusion body myopathy with early onset Paget disease and frontotemporal dementia", "Inclusion Body Myopathy with Early-Onset Paget Disease of Bone and-or Frontotemporal Dementia", "Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia (disorder)", "Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia (diagnosis)", "inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inclusion body myopathy with Paget disease of bone and frontotemporal dementia", "shortest_name_length": 6}
{"curie": "UMLS:C0346564", "names": ["Base of Tongue Carcinoma", "Posterior Tongue Carcinoma", "Carcinoma of Base of Tongue", "Carcinoma of base of tongue", "Base of the Tongue Carcinoma", "Carcinoma of Posterior Tongue", "Carcinoma of the Posterior Tongue", "Carcinoma of the Base of the Tongue", "Carcinoma of base of tongue (disorder)", "Carcinoma of base of tongue (diagnosis)", "tongue neoplasm malignant carcinoma at base"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carcinoma of base of tongue", "shortest_name_length": 24}
{"curie": "MONDO:0015307", "names": ["MMND", "Madras motor neuron disease", "Madras-type motor neurone disease", "Madras-type motor neurone disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Madras motor neuron disease", "shortest_name_length": 4}
{"curie": "UMLS:C5206824", "names": ["Resectable Oropharyngeal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Oropharyngeal Squamous Cell Carcinoma", "shortest_name_length": 48}
{"curie": "MONDO:0023275", "names": ["Graham-Boyle-Troxell syndrome", "Graham Boyle Troxell syndrome", "graham Boyle Troxell syndrome", "Cystic hamartoma of lung and kidney", "cystic hamartoma of lung and kidney", "cystic hamartomata of lung and kidney", "Cystic hamartomata of lung and kidney", "Cystic hamartoma of lung and kidney (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Graham-Boyle-Troxell syndrome", "shortest_name_length": 29}
{"curie": "UMLS:C0581394", "names": ["Swollen;leg", "swollen leg", "Swollen leg", "leg swollen", "swollen legs", "Leg swelling", "leg swelling", "legs swelling", "swelling; leg", "leg; swelling", "swollen feet leg", "Swelling of legs", "swelling of legs", "swollen feet/legs", "swollen legs feet", "feet legs swollen", "Hindlimb swelling", "swollen feet legs", "legs feet swollen", "Swelling of lower limb", "LOWER EXTREMITY SWOLLEN", "lower extremity swelling", "LOWER EXTREMITY SWELLING", "Swelling of lower extremities", "Swelling of lower limb (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Swelling of lower limb", "shortest_name_length": 11}
{"curie": "UMLS:C5418899", "names": ["Recurrent Mucosal Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Mucosal Melanoma", "shortest_name_length": 26}
{"curie": "UMLS:C0685895", "names": ["Rhinocephaly", "RHINOCEPHALY", "Rhinocephaly (disorder)", "Rhinocephaly (diagnosis)", "congenital anomalies of respiratory system rhinocephaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rhinocephaly", "shortest_name_length": 12}
{"curie": "MONDO:0016126", "names": ["myositis viral", "VIRAL MYOSITIS", "viral myositis", "Viral myositis", "Viral myositis (disorder)", "viral myositis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "viral myositis", "shortest_name_length": 14}
{"curie": "UMLS:C5428719", "names": ["Malignant Lacrimal System Neoplasm", "Malignant Lacrimal Apparatus Neoplasm", "malignant neoplasm of lacrimal apparatus", "eye neoplasm malignant lacrimal apparatus", "malignant neoplasm of lacrimal apparatus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant neoplasm of lacrimal apparatus", "shortest_name_length": 34}
{"curie": "UMLS:C1710415", "names": ["Thyroid Gland Mucinous Follicular Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Mucinous Follicular Adenoma", "shortest_name_length": 41}
{"curie": "MONDO:0018841", "names": ["CBA", "BASD", "Congenital bile acid synthesis defect", "congenital bile acid synthesis defect", "bile acid synthesis defect, congenital", "3-beta-hydroxy-delta-5-C27-steroid oxidoreductase deficiency", "cholestasis with delta(4)-3-oxosteroid-5-beta-reductase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital bile acid synthesis defect", "shortest_name_length": 3}
{"curie": "UMLS:C3897940", "names": ["Anti-Mullerian Hormone Resistance", "Persistent Mullerian Duct Syndrome Type 2", "Persistent Mullerian Duct Syndrome Type II", "PERSISTENT MULLERIAN DUCT SYNDROME, TYPE II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PERSISTENT MULLERIAN DUCT SYNDROME, TYPE II", "shortest_name_length": 33}
{"curie": "MONDO:0100076", "names": ["juvenile idiopathic scoliosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile idiopathic scoliosis", "shortest_name_length": 29}
{"curie": "UMLS:C0030922", "names": ["pu bleeding", "Bleeding PU", "bleeding pus", "bleeding peptic ulcer", "Bleeding peptic ulcer", "ULCER BLEEDING PEPTIC", "Ulcer bleeding peptic", "peptic ulcer bleeding", "peptic ulcer hemorrhage", "PEPTIC ULCER HEMORRHAGE", "Peptic Ulcer Hemorrhage", "Peptic ulcer hemorrhage", "Ulcer Hemorrhage, Peptic", "PEPTIC ULCER HEMORRHAGIC", "Peptic ulcer hemorrhagic", "Hemorrhage, Peptic Ulcer", "Peptic ulcer haemorrhage", "Peptic Ulcer Hemorrhages", "PEPTIC ULCER HAEMORRHAGIC", "Peptic ulcer haemorrhagic", "Ulcer peptic with hemorrhage", "PEPTIC ULCER WITH HEMORRHAGE", "ULCER PEPTIC WITH HEMORRHAGE", "Peptic ulcer with hemorrhage", "Peptic ulcer with haemorrhage", "Ulcer peptic with haemorrhage", "peptic; ulcer, with hemorrhage", "ulcer; peptic, with hemorrhage", "Peptic ulcer, NOS with hemorrhage", "Peptic ulcer, NOS with haemorrhage", "Peptic ulcer with hemorrhage (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peptic Ulcer Hemorrhage", "shortest_name_length": 11}
{"curie": "MONDO:0004256", "names": ["lumbar intraspinal meningioma", "Lumbar Intraspinal Meningioma", "lumbar spinal canal and spinal cord meningioma", "Lumbar Spinal Canal and Spinal Cord Meningioma", "Meningioma of Lumbar Spinal Canal and Spinal Cord", "meningioma of lumbar spinal canal and spinal cord", "meningioma of Lumbar Spinal canal and Spinal Cord", "Meningioma of the Lumbar Spinal Canal and Spinal Cord", "meningioma of the lumbar spinal canal and spinal cord"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lumbar spinal canal and spinal cord meningioma", "shortest_name_length": 29}
{"curie": "MONDO:0011377", "names": ["LQT3", "LQT3 syndrome", "LQT2/3, DIGENIC", "LONG QT SYNDROME 3", "long QT syndrome 3", "Long QT Syndrome 3", "Long Qt Syndrome 3", "SCN5A long QT syndrome", "Long QT syndrome type 3", "long QT syndrome type 3", "LQT3 syndrome (diagnosis)", "long QT syndrome 3/6, digenic", "LONG QT SYNDROME 2/3, DIGENIC", "long QT syndrome 2/3, digenic", "Long QT syndrome type 3 (disorder)", "long QT syndrome caused by mutation in SCN5A", "LONG QT SYNDROME 3, ACQUIRED, SUSCEPTIBILITY TO", "long QT syndrome 3, acquired, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "long QT syndrome 3", "shortest_name_length": 4}
{"curie": "UMLS:C5447756", "names": ["Immune Checkpoint Inhibitor-related Myocarditis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immune Checkpoint Inhibitor-related Myocarditis", "shortest_name_length": 47}
{"curie": "UMLS:C1510741", "names": ["Abscess Leakage", "Abscess Spillage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abscess Leakage", "shortest_name_length": 15}
{"curie": "MONDO:0009165", "names": ["Ags", "AGS1", "Cree encephalitis", "Cree Encephalitis", "Pseudotoxoplasmosis syndrome", "Pseudotoxoplasmosis Syndrome", "AICARDI-GOUTIERES SYNDROME 1", "Aicardi-Goutieres Syndrome 1", "Aicardi-Goutieres syndrome 1", "TREX1 Aicardi-Goutieres syndrome", "Aicardi-Goutieres syndrome type 1", "Aicardi-Goutieres syndrome 1, autosomal dominant", "AICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT", "Aicardi-Goutieres syndrome 1, dominant and recessive", "Aicardi-Goutieres syndrome caused by mutation in TREX1", "encephalopathy, familial infantile, with intracranial calcification and chronic cerebrospinal fluid lymphocytosis", "Encephalopathy, Familial Infantile, with Intracranial Calcification and Chronic Cerebrospinal Fluid Lymphocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aicardi-Goutieres syndrome 1", "shortest_name_length": 3}
{"curie": "UMLS:C4520954", "names": ["stage IV gallbladder cancer", "Stage IV Gallbladder Cancer", "Stage IV Gallbladder Cancer AJCC v7", "Stage IV Gallbladder Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Gallbladder Cancer AJCC v7", "shortest_name_length": 27}
{"curie": "MONDO:0030733", "names": ["SPGF70", "spermatogenic failure 70", "SPERMATOGENIC FAILURE 70"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 70", "shortest_name_length": 6}
{"curie": "MONDO:0009290", "names": ["AMD", "GSD2", "GSD2s", "Pompe", "GSD 2", "GSD II", "GSD IIIc", "GSD IIIC", "GSD type 2", "GSD type II", "Pompe disease", "pompe disease", "POMPE DISEASE", "Pompe Disease", "Disease, Pompe", "GAA deficiency", "Pompes Disease", "2 glycogenosis", "GAA Deficiency", "pompes disease", "GAA DEFICIENCY", "Glycogenosis 2", "disease pompe's", "Pompe's disease", "pompe's disease", "Deficiency, GAA", "Pompe's Disease", "Disease, Pompe's", "GAA Deficiencies", "Aglucosidase alfa", "Deficiencies, GAA", "maltase deficiency", "Glycogenosis type 2", "glycogenosis type 2", "glycogenosis, type 2", "Glycogenosis Type II", "Glycogenosis type II", "glycogenosis type II", "Glycogenosis, type 2", "Type II, Glycogenosis", "deficiency of maltase", "GLYCOGENOSIS, TYPE II", "Glycogen heart disease", "Type IIs, Glycogenosis", "maltase acid deficiency", "Acid maltase deficiency", "ACID MALTASE DEFICIENCY", "acid maltase deficiency", "Generalized Glycogenosis", "Generalized Glycogenoses", "Generalized glycogenosis", "generalized glycogenosis", "Glycogenoses, Generalized", "Glycogenosis, Generalized", "Glycogen storage disease 2", "deficiency of glucoamylase", "glycogen storage disease 2", "GLYCOGEN STORAGE DISEASE II", "Glycogen Storage Disease II", "glycogen storage disease II", "ALPHA-GLUCOSIDASE DEFICIENCY", "GAA glycogen storage disease", "Alpha-Glucosidase Deficiency", "alpha-Glucosidase deficiency", "ALPHA GLUCOSIDASE DEFICIENCY", "AMD - Acid maltase deficiency", "GLYCOGEN STORAGE DISEASE IIIc", "Glycogen Storage Disease IIIC", "Alpha-Glucosidase Deficiencies", "Glycogen Storage Disease Type 2", "Deficiency of Alpha Glucosidase", "Glycogen storage disease type 2", "acid maltase deficiency disease", "Deficiency of Alpha-Glucosidase", "deficiency of alpha-glucosidase", "glycogen storage disease type 2", "Acid Maltase Deficiency Disease", "glycogen storage disease type II", "Type II glycogen storage disease", "Alpha-1,4-glucosidase deficiency", "alpha 1,4 glucosidase deficiency", "LYSOSOMAL GLUCOSIDASE DEFICIENCY", "glycogen storage disease type ii", "ALPHA-1,4-GLUCOSIDASE DEFICIENCY", "Glycogen storage disease type II", "Deficiency Disease, Acid Maltase", "Glycogen Storage Disease Type II", "GLYCOGEN STORAGE DISEASE TYPE II", "alpha-1,4-Glucosidase deficiency", "CARDIOMEGALIA GLYCOGENICA DIFFUSA", "Cardiomegalia Glycogenica diffusa", "Glycogen storage disease, type II", "ACID ALPHA-GLUCOSIDASE DEFICIENCY", "Cardiomegalia glycogenica diffusa", "glycogen storage disease, type II", "Acid Alpha-Glucosidase Deficiency", "Acid Alpha Glucosidase Deficiency", "GSD due to acid maltase deficiency", "Alpha-Glucosidase Deficiency, Acid", "Deficiency, Acid Alpha-Glucosidase", "Acid Alpha-Glucosidase Deficiencies", "Alpha-Glucosidase Deficiencies, Acid", "Deficiencies, Acid Alpha-Glucosidase", "Alpha-1,4-glucosidase acid deficiency", "glucosidase acid-1,4-alpha deficiency", "GLYCOGENOSIS, GENERALIZED, CARDIAC FORM", "Glycogenosis, Generalized, Cardiac Form", "glycogenosis, generalized, Cardiac form", "Cardiac form of generalized glycogenosis", "deficiency of lysosomal alpha-glucosidase", "lysosomal alpha-1,4-glucosidase deficiency", "Lysosomal alpha-1,4-glucosidase deficiency", "glycogenosis due to acid maltase deficiency", "Glycogenosis due to acid maltase deficiency", "glycogen storage disease type II (diagnosis)", "Glycogen storage disease, type II (disorder)", "Generalized glycogen storage disease of infants", "glycogen storage disease caused by mutation in GAA", "Lysosomal alpha-1,4-Glucosidase Deficiency Disease", "Lysosomal alpha 1,4 Glucosidase Deficiency Disease", "Deficiency Disease, Lysosomal alpha-1,4-Glucosidase", "glycogen storage disease due to acid maltase deficiency", "Glycogen storage disease due to acid maltase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease II", "shortest_name_length": 3}
{"curie": "UMLS:C5556345", "names": ["Tectal Glioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tectal Glioma", "shortest_name_length": 13}
{"curie": "MONDO:0003787", "names": ["Pediatric Testicular Mixed Germ Cell Tumor", "Childhood Testicular Mixed Germ Cell Tumor", "pediatric testicular mixed germ cell tumor", "childhood testicular mixed germ cell tumor", "childhood testicular mixed germ cell tumour", "childhood mixed testicular germ cell cancer", "pediatric mixed testicular germ cell cancer", "childhood testicular mixed germ cell cancer", "paediatric testicular mixed germ cell tumour", "pediatric testicular mixed germ cell neoplasm", "Pediatric Testicular Mixed Germ Cell Neoplasm", "Childhood Testicular Mixed Germ Cell Neoplasm", "childhood testicular mixed germ cell neoplasm", "mixed testicular germ cell cancer of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood testicular mixed germ cell cancer", "shortest_name_length": 42}
{"curie": "MONDO:0016819", "names": ["Moebius axonal neuropathy hypogonadism", "Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome", "shortest_name_length": 38}
{"curie": "MONDO:0012776", "names": ["CELIAC7", "CELIAC DISEASE, SUSCEPTIBILITY TO, 7", "celiac disease, susceptibility to, 7", "GLUTEN-SENSITIVE ENTEROPATHY, SUSCEPTIBILITY TO, 7", "gluten-sensitive enteropathy, susceptibility to, 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "celiac disease, susceptibility to, 7", "shortest_name_length": 7}
{"curie": "UMLS:C0751604", "names": ["SPASTIC PARAPLEGIA 2", "Spastic Paraplegia 2", "Spastic Paraplegia Type 2", "Hereditary X Linked Recessive Spastic Paraplegia", "Hereditary X-Linked Recessive Spastic Paraplegia", "X-linked Recessive Hereditary Spastic Paraplegia", "X Linked Recessive Hereditary Spastic Paraplegia", "Spastic Paraplegia, X-Linked Recessive, Hereditary", "Hereditary, Spastic Paraplegia, X-Linked Recessive", "Spastic Paraplegia, Hereditary, X-Linked Recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hereditary X-Linked Recessive Spastic Paraplegia", "shortest_name_length": 20}
{"curie": "MONDO:0006078", "names": ["AIDS-Related Primary CNS Lymphoma", "AIDS-related primary CNS lymphoma", "AIDS related primary CNS lymphoma", "AIDS Related Primary CNS Lymphoma", "primary CNS lymphoma, AIDS-related", "AIDS Related Primary Central Nervous System Lymphoma", "AIDS-Related Primary Central Nervous System Lymphoma", "AIDS-related primary central nervous system lymphoma", "AIDS related primary central nervous system lymphoma", "AIDS-related lymphoma of primary central nervous system", "AIDS related lymphoma of primary central nervous system", "AIDS-Related Lymphoma of Primary Central Nervous System", "AIDS Related Lymphoma of Primary Central Nervous System", "AIDS-related lymphoma of the primary central nervous system", "AIDS related lymphoma of the primary central nervous system", "AIDS-Related Lymphoma of the Primary Central Nervous System", "AIDS Related Lymphoma of the Primary Central Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-related primary central nervous system lymphoma", "shortest_name_length": 33}
{"curie": "UMLS:C0221765", "names": ["Chronic schizophrenia", "CHRONIC SCHIZOPHRENIA", "SCHIZOPHRENIA CHRONIC", "Chronic Schizophrenia", "chronic schizophrenic", "chronic schizophrenia", "Chronic schizophrenic", "Chronic schizophrenia, NOS", "Chronic schizophrenia (disorder)", "chronic schizophrenia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic schizophrenia", "shortest_name_length": 21}
{"curie": "MONDO:0042604", "names": ["Sandhaus-Ben-Ami syndrome", "Sandhaus Ben-Ami syndrome", "Patella hypoplasia skeletal malformations", "patella hypoplasia skeletal malformations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sandhaus-Ben-Ami syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0017490", "names": ["tibial hemimelia, unilateral", "tibial longitudinal meromelia, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tibial hemimelia, unilateral", "shortest_name_length": 28}
{"curie": "UMLS:C4329631", "names": ["Central Nervous System Erdheim-Chester Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Erdheim-Chester Disease", "shortest_name_length": 46}
{"curie": "UMLS:C0518959", "names": ["left atrial myxoma", "atrial left myxoma", "ATRIAL MYXOMA LEFT", "Left atrial myxoma", "atrial myxoma left", "Left Atrial Myxoma", "atrial left myxomas", "Myxoma of Left Atrium", "myxoma of left atrium", "Myxoma of the Left Atrium", "myxoma of left atrium (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Left atrial myxoma", "shortest_name_length": 18}
{"curie": "UMLS:C1708960", "names": ["Mediastinal Solitary Fibrous Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mediastinal Solitary Fibrous Tumor", "shortest_name_length": 34}
{"curie": "UMLS:C3888446", "names": ["Stoma site discharge", "Stoma site secretion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stoma site discharge", "shortest_name_length": 20}
{"curie": "MONDO:0004983", "names": ["SPGF", "spermatogenic failure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure", "shortest_name_length": 4}
{"curie": "MONDO:0015941", "names": ["Finucane Kurtz Scott syndrome", "Finucane-Kurtz-Scott syndrome", "epiphyseal dysplasia hearing loss dysmorphism", "Epiphyseal dysplasia-deafness-dysmorphism syndrome", "epiphyseal dysplasia-hearing loss-dysmorphism syndrome", "Epiphyseal dysplasia-hearing loss-dysmorphism syndrome", "Epiphyseal dysplasia, hearing loss, dysmorphism syndrome", "Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder)", "Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (diagnosis)", "multiple malformation syndrome epiphyseal dysplasia, hearing loss, dysmorphism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epiphyseal dysplasia-hearing loss-dysmorphism syndrome", "shortest_name_length": 29}
{"curie": "MONDO:0100274", "names": ["AGPS deficiency", "alkylglycerone-phosphate synthase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alkylglycerone-phosphate synthase deficiency", "shortest_name_length": 15}
{"curie": "MONDO:0014641", "names": ["FTDALS4", "FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4", "frontotemporal dementia and/or amyotrophic lateral sclerosis-4", "frontotemporal dementia and/or amyotrophic lateral sclerosis 4", "frontotemporal dementia and/or amyotrophic lateral sclerosis type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontotemporal dementia and/or amyotrophic lateral sclerosis 4", "shortest_name_length": 7}
{"curie": "UMLS:C1290140", "names": ["PSRA", "Post-Streptococcal Arthritis", "Post-Streptococcal Reactive Arthritis", "Post-streptococcal reactive arthritis", "post-streptococcal reactive arthritis", "Post-streptococcal reactive arthritis (disorder)", "post-streptococcal reactive arthritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post-streptococcal reactive arthritis", "shortest_name_length": 4}
{"curie": "MONDO:0018710", "names": ["megalencephaly-severe kyphoscoliosis-overgrowth syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "megalencephaly-severe kyphoscoliosis-overgrowth syndrome", "shortest_name_length": 56}
{"curie": "UMLS:C4744384", "names": ["Pituitary Gland Diffuse Large B-Cell Lymphoma", "Primary Pituitary Gland Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pituitary Gland Diffuse Large B-Cell Lymphoma", "shortest_name_length": 45}
{"curie": "UMLS:C0576091", "names": ["knee deformity", "Knee deformity", "deformity knee", "KNEE DEFORMITY", "knee; deformity", "Stifle deformed", "deformity; knee", "Knee deformities", "deformities knee", "deformity of knee", "Deformity of Knees", "Knee deformity NOS", "Deformity of knee NOS", "Deformity of knee joint", "Deformity of knee joint (finding)", "deformity of knee (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Deformity of knee joint", "shortest_name_length": 14}
{"curie": "MONDO:0014138", "names": ["NEM8", "Nemaline Myopathy 8", "NEMALINE MYOPATHY 8", "nemaline myopathy 8", "nemaline myopathy type 8", "KLHL40 nemaline myopathy", "nemaline myopathy 8, autosomal recessive", "nemaline myopathy caused by mutation in KLHL40"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nemaline myopathy 8", "shortest_name_length": 4}
{"curie": "MONDO:0004972", "names": ["Adenoma", "adenoma", "ADENOMA", "adenomas", "Adenomas", "ADENOMA NOS", "Adenoma NOS", "Adenoma, NOS", "Acinar Adenoma", "Benign adenoma", "Acinar adenoma", "benign adenoma", "Adenoma benign", "ADENOMA, BENIGN", "adenoma, benign", "Adenoma benign NOS", "tumor of the gland", "Acinic Cell Adenoma", "Acinar cell adenoma", "acinic cell adenoma", "acinar cell adenoma", "Acinar Cell Adenoma", "Acinic cell adenoma", "Benign adenoma (disorder)", "Benign adenomatous neoplasm", "ADENOMA, ACINAR CELL, BENIGN", "Adenoma (morphologic abnormality)", "Benign adenomatous neoplasm (disorder)", "acinar cell adenoma (morphologic abnormality)", "Acinar cell adenoma (morphologic abnormality)", "Benign adenomatous neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenoma", "shortest_name_length": 7}
{"curie": "MONDO:0019667", "names": ["spondyloepiphyseal dysplasia tarda", "X-linked spondyloepiphyseal dysplasia tarda"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepiphyseal dysplasia tarda", "shortest_name_length": 34}
{"curie": "MONDO:0003529", "names": ["Acute pyelonephritis", "pyelonephritis acute", "Acute Pyelonephritis", "PYELONEPHRITIS ACUTE", "Pyelonephritis acute", "acute pyelonephritis", "pyelonephritis; acute", "pyelonephritis, acute", "PYELONEPHRITIS, ACUTE", "acute; pyelonephritis", "Acute kidney infection", "Pyelonephritis acute NOS", "Acute PN - pyelonephritis", "APN - Acute pyelonephritis", "Acute pyelonephritis (disorder)", "Acute pyelonephritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute pyelonephritis", "shortest_name_length": 20}
{"curie": "MONDO:0005634", "names": ["Apollo disease", "viral conjunctivitis", "Apollo conjunctivitis", "Apollo; disease (etiology)", "Apollo; disease (manifestation)", "ACUTE HEMORRHAGIC CONJUNCTIVITIS", "conjunctivitis acute hemorrhagic", "acute hemorrhagic conjunctivitis", "Acute hemorrhagic conjunctivitis", "Acute Hemorrhagic Conjunctivitis", "Acute haemorrhagic conjunctivitis", "conjunctivitis; Apollo (etiology)", "Apollo conjunctivitis (diagnosis)", "Hemorrhagic Conjunctivitis, Acute", "Apollo; conjunctivitis (etiology)", "Conjunctivitis, Acute Hemorrhagic", "Acute Hemorrhagic Conjunctivitides", "CONJUNCTIVITIS, HEMORRHAGIC, ACUTE", "Hemorrhagic Conjunctivitides, Acute", "Epidemic hemorrhagic conjunctivitis", "Conjunctivitides, Acute Hemorrhagic", "epidemic hemorrhagic conjunctivitis", "Epidemic haemorrhagic conjunctivitis", "CONJUNCTIVITIS, EPIDEMIC HEMORRHAGIC", "Enteroviral hemorrhagic conjunctivitis", "Apollo; conjunctivitis (manifestation)", "AHC - Acute hemorrhagic conjunctivitis", "conjunctivitis; Apollo (manifestation)", "Enteroviral haemorrhagic conjunctivitis", "AHC - Acute haemorrhagic conjunctivitis", "disease (or disorder); Apollo (etiology)", "EHC - Epidemic hemorrhagic conjunctivitis", "EHC - Epidemic haemorrhagic conjunctivitis", "Acute hemorrhagic conjunctivitis (disorder)", "acute hemorrhagic conjunctivitis (diagnosis)", "disease (or disorder); Apollo (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute hemorrhagic conjunctivitis", "shortest_name_length": 14}
{"curie": "MONDO:0021003", "names": ["Polydactyly", "polydactyly", "POLYDACTYLY", "Hyperdactyly", "hyperdactyly", "Polydactylia", "polydactylia", "Polydactylias", "polydactylism", "Polydactylies", "Polydactylism", "Hyperdactylies", "Polydactylisms", "Accessory digit", "Multiple digits", "multiple; digits", "Polydactyly, NOS", "supernumerary digit", "Supernumerary digit", "supernumerary digits", "Supernumerary digits", "polydactyly (disease)", "postaxial polydactyly", "Polydactyly (disorder)", "polydactyly (diagnosis)", "Polydactyly, unspecified", "Non-syndromic polydactyly", "Supernumerary digit(s) NOS", "Polydactyly, unspecified digits", "More than five fingers or toes on hands or feet"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polydactyly", "shortest_name_length": 11}
{"curie": "DOID:0080839", "names": ["X-linked warfarin sensitivity", "COUMARIN SENSITIVITY, X-LINKED", "WARFARIN SENSITIVITY, X-LINKED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked warfarin sensitivity", "shortest_name_length": 29}
{"curie": "MONDO:0013697", "names": ["MRT29", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 29", "mental retardation, autosomal recessive 29", "intellectual disability, autosomal recessive 29", "autosomal recessive intellectual developmental disorder 29", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 29"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 29", "shortest_name_length": 5}
{"curie": "MONDO:0000471", "names": ["Tricuspid disease", "tricuspid disease", "Tricuspid valve disease", "Tricuspid Valve Disease", "tricuspid valve disease", "Tricuspid valve disorder", "Tricuspid valve abnormal", "tricuspid valve disorder", "Tricuspid Valve Disorder", "tricuspid valve disorders", "disease of tricuspid valve", "Tricuspid valve disease NOS", "disorder of tricuspid valve", "Diseases of tricuspid valve", "RH. tricuspid valve disease", "Tricuspid valve disorder, NOS", "Rheumatic tricuspid valve disease", "rheumatic tricuspid valve disease", "Tricuspid valve rheumatic disease", "rheumatic tricuspid valve disorder", "Rheumatic tricuspid valve diseases", "tricuspid valve disease or disorder", "Tricuspid valve disorder (disorder)", "Tricuspid valve disease, unspecified", "rheumatic disease of tricuspid valve", "tricuspid valve disorder (diagnosis)", "Rheumatic disease of tricuspid valve", "Rheumatic tricuspid valve disease, NOS", "Rheumatic tricuspid valve disorder NOS", "disease or disorder of tricuspid valve", "tricuspid (valve); disorder (rheumatic)", "Rheumatic disease of tricuspid valve, NOS", "rheumatic tricuspid valve disorder (diagnosis)", "Rheumatic disease of tricuspid valve (disorder)", "disease (or disorder); tricuspid (valve) (rheumatic)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tricuspid valve disorder", "shortest_name_length": 17}
{"curie": "UMLS:C0751188", "names": ["Postdural Puncture Headache", "postdural puncture headache", "post dural puncture headache", "Post-dural puncture headache", "post-dural puncture headache", "dural headache post puncture", "Headache, Postdural Puncture", "Post-Dural Puncture Headache", "Post Dural Puncture Headache", "Postdural Puncture Headaches", "Post dural puncture headache", "dural headaches post puncture", "Post-Dural Puncture Headaches", "Headache, Post-Dural Puncture", "Headaches, Postdural Puncture", "Headaches, Post-Dural Puncture", "PDPH - Post dural puncture headache", "Post dural puncture headache (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post-Dural Puncture Headaches", "shortest_name_length": 27}
{"curie": "MONDO:0020444", "names": ["subaortic course of innominate vein", "Subaortic course of innominate vein", "subaortic course of brachiocephalic vein", "Subaortic course of brachiocephalic vein", "Subaortic course of innominate vein (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subaortic course of innominate vein", "shortest_name_length": 35}
{"curie": "UMLS:C4525354", "names": ["IIIB", "Stage IIIB Intrahepatic Cholangiocarcinoma AJCC v8", "Stage IIIB Intrahepatic Bile Duct Cancer (Cholangiocarcinoma)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Intrahepatic Cholangiocarcinoma AJCC v8", "shortest_name_length": 4}
{"curie": "MONDO:0011873", "names": ["NPC2", "type C2 Niemann-Pick disease", "Type C2 Niemann-Pick Disease", "Niemann-Pick disease type C2", "NIEMANN-PICK DISEASE, TYPE C2", "Niemann-Pick disease, type C2", "Niemann-PICK disease, type C2", "Niemann-Pick Disease, Type C2", "Niemann-Pick disease type C2 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Niemann-Pick disease, type C2", "shortest_name_length": 4}
{"curie": "UMLS:C1142115", "names": ["infectious enterocolitis", "Enterocolitis infectious", "Infectious Enterocolitis", "infectious enterocolitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infectious Enterocolitis", "shortest_name_length": 24}
{"curie": "UMLS:C5206777", "names": ["Refractory Dedifferentiated Chordoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Dedifferentiated Chordoma", "shortest_name_length": 36}
{"curie": "MONDO:0018210", "names": ["AxD type II", "Alexander disease type II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alexander disease type II", "shortest_name_length": 11}
{"curie": "UMLS:C0577618", "names": ["allergy perfume", "Perfume allergy", "perfume allergy", "allergy perfumes", "allergies perfume", "Perfume sensitivity", "perfume sensitivities", "perfumes sensitivities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perfume sensitivity", "shortest_name_length": 15}
{"curie": "UMLS:C5556870", "names": ["Female Reproductive System Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Female Reproductive System Carcinoma", "shortest_name_length": 36}
{"curie": "UMLS:C4524522", "names": ["Stage II", "Stage II Head and Neck Squamous Cell Cancer", "Stage II Cutaneous Squamous Cell Carcinoma of the Head and Neck AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Cutaneous Squamous Cell Carcinoma of the Head and Neck AJCC v8", "shortest_name_length": 8}
{"curie": "MONDO:0800095", "names": ["syndrome with synostosis or other joint formation defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndrome with synostosis or other joint formation defect", "shortest_name_length": 56}
{"curie": "UMLS:C0494827", "names": ["Childhood linear IgA disease", "Childhood Linear IgA Disease", "Chronic Bullous Disease of Childhood", "Chronic bullous disease of childhood", "bullous; disorder, chronic, childhood", "chronic; bullous disease of childhood", "Linear IgA bullous disease in children", "Linear IgA bullous disease of childhood", "Chronic bullous dermatosis of childhood", "Benign chronic bullous dermatosis of childhood", "Chronic bullous dermatosis of childhood (disorder)", "disease (or disorder); bullous, chronic, childhood", "disease (or disorder); chronic bullous of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic Bullous Disease of Childhood", "shortest_name_length": 28}
{"curie": "UMLS:C4054113", "names": ["Recurrent Childhood Lymphomatoid Granulomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Lymphomatoid Granulomatosis", "shortest_name_length": 47}
{"curie": "UMLS:C1704315", "names": ["Necrotizing Pyelonephritis", "PYELONEPHRITIS ACUTE NECROTIZING", "Pyelonephritis acute necrotizing", "Pyelonephritis acute necrotising", "PYELONEPHRITIS ACUTE NECROTISING", "Pyelonephritis, Acute Necrotizing"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pyelonephritis acute necrotizing", "shortest_name_length": 26}
{"curie": "UMLS:C3897045", "names": ["SHOX Deficiency", "Short Stature Homeobox Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Short Stature Homeobox Deficiency", "shortest_name_length": 15}
{"curie": "UMLS:C0348898", "names": ["bowel; irritable, with diarrhea", "irritable bowel syndrome; diarrhea", "diarrhea; irritable bowel syndrome", "irritability; bowel, with diarrhea", "Irritable bowel syndrome with diarrhea", "irritable bowel syndrome with diarrhea", "Irritable bowel syndrome with diarrhoea", "syndrome; irritable bowel, with diarrhea", "Irritable bowel syndrome with diarrhea (disorder)", "irritable bowel syndrome with diarrhea (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Irritable bowel syndrome with diarrhea", "shortest_name_length": 31}
{"curie": "MONDO:0021472", "names": ["Benign Scrotal Tumor", "benign scrotal tumor", "benign scrotal neoplasm", "scrotum benign neoplasm", "Benign Tumor of Scrotum", "Benign Scrotal Neoplasm", "benign tumor of scrotum", "benign neoplasm of scrotum", "Benign Neoplasm of Scrotum", "Benign neoplasm of scrotum", "benign tumor of the scrotum", "Benign scrotal neoplasm NOS", "Benign Tumor of the Scrotum", "Benign Neoplasm of the Scrotum", "benign neoplasm of the scrotum", "Benign neoplasm of scrotum (disorder)", "benign neoplasm of scrotum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of scrotum", "shortest_name_length": 20}
{"curie": "MONDO:0000989", "names": ["MUMPS", "mumps", "Mumps", "Mumps NOS", "Mumps, NOS", "Clinical mumps", "Mumps parotitis", "mumps parotitis", "Mumps (disorder)", "mumps (diagnosis)", "EPIDEMIC PAROTITIS", "parotitis epidemic", "Epidemic Parotitis", "Epidemic parotitis", "epidemic parotitis", "Parotitis, Epidemic", "parotitis; epidemic", "Mumps parotitis NOS", "epidemic; parotitis", "Infectious parotitis", "infectious parotitis", "parotitis infectious", "epidemic parotiditis", "Epidemic Parotitides", "Rubulavirus infection", "parotitis; infectious", "Parotitides, Epidemic", "infectious; parotitis", "Rubulavirus Infection", "Infection, Rubulavirus", "Rubulavirus Infections", "Infections, Rubulavirus", "mumps infectious disease", "Mumps parotitis (disorder)", "epidemic parotitis (diagnosis)", "mumps virus infectious disease", "Mumps virus infectious disease", "Infection caused by Rubulavirus", "Mumps virus disease or disorder", "infectious parotitis (diagnosis)", "Mumps virus caused disease or disorder", "Infection caused by Rubulavirus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mumps infectious disease", "shortest_name_length": 5}
{"curie": "MONDO:0013646", "names": ["Del(8)(q21.11)", "deletion 8q21.11", "Deletion 8q21.11", "monosomy 8q21.11", "Monosomy 8q21.11", "8q21.11 microdeletion syndrome", "chromosome 8q21.11 deletion syndrome", "CHROMOSOME 8q21.11 DELETION SYNDROME", "8q21.11 microdeletion syndrome (disorder)", "chromosome 8q21.11 deletion syndrome, isolated cases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 8q21.11 deletion syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0009686", "names": ["MUSK, INABILITY TO SMELL", "Musk, Inability to Smell", "musk, inability to smell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "musk, inability to smell", "shortest_name_length": 24}
{"curie": "UMLS:C5446551", "names": ["Secondary Choroidal Lymphoma", "Secondary Choroidal Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary Choroidal Non-Hodgkin Lymphoma", "shortest_name_length": 28}
{"curie": "UMLS:C4331342", "names": ["Stage IVB Lip and Oral Cavity Cancer", "Stage IVB Lip and Oral Cavity Cancer AJCC v8", "Stage IVB Lip and Oral Cavity Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Lip and Oral Cavity Cancer AJCC v8", "shortest_name_length": 36}
{"curie": "MONDO:0035459", "names": ["idiopathic multidrug-resistant nephrotic syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic multidrug-resistant nephrotic syndrome", "shortest_name_length": 49}
{"curie": "UMLS:C3640030", "names": ["Congenital SVT", "Congenital Supraventricular Tachycardia", "Congenital supraventricular tachycardia", "Supraventricular Tachycardia (SVT), Congential", "Supraventricular Tachycardia (SVT), Congenital"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital supraventricular tachycardia", "shortest_name_length": 14}
{"curie": "MONDO:0009408", "names": ["Hyperuricemia, Infantile, with Abnormal Behavior and Normal Hypoxanthine Guanine Phosphoribosyltransferase", "HYPERURICEMIA, INFANTILE, WITH ABNORMAL BEHAVIOR AND NORMAL HYPOXANTHINE GUANINE PHOSPHORIBOSYLTRANSFERASE", "hyperuricemia, infantile, with abnormal behavior and normal hypoxanthine guanine phosphoribosyltransferase"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperuricemia, infantile, with abnormal behavior and normal hypoxanthine guanine phosphoribosyltransferase", "shortest_name_length": 106}
{"curie": "MONDO:0006780", "names": ["Cowdriosis", "COWDRIOSES", "Heartwater", "heartwater disease", "Heartwater Disease", "Disease, Heartwater", "disease, heartwater", "Heartwater (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heartwater disease", "shortest_name_length": 10}
{"curie": "UMLS:C0521492", "names": ["Application site ulcer", "Application site ulcer (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Application site ulcer", "shortest_name_length": 22}
{"curie": "UMLS:C0234944", "names": ["ANESTHESIA INJECTION SITE", "INJECTION SITE ANESTHESIA", "Injection site anesthesia", "Anesthesia injection site", "INJECTION SITE ANAESTHESIA", "Anaesthesia injection site", "Injection site anaesthesia", "Injection site anesthesia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site anesthesia", "shortest_name_length": 25}
{"curie": "UMLS:C2063616", "names": ["DITP", "Drug-Induced Thrombocytopenia", "Drug Induced Thrombocytopenia", "drug-induced thrombocytopenia", "Drug-Induced Immune Thrombocytopenia", "drug-induced thrombocytopenia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drug Induced Thrombocytopenia", "shortest_name_length": 4}
{"curie": "UMLS:C0521501", "names": ["Injection site thrombosis", "Injection site thrombosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site thrombosis", "shortest_name_length": 25}
{"curie": "UMLS:C5239287", "names": ["Locally Advanced Biliary Tract Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Biliary Tract Carcinoma", "shortest_name_length": 40}
{"curie": "UMLS:C2030354", "names": ["Heart Angiosarcoma", "cardiac angiosarcoma", "Cardiac Angiosarcoma", "angiosarcoma of heart", "cardiac hemangiosarcoma", "Cardiac hemangiosarcoma", "Hemangiosarcoma of heart", "hemangiosarcoma of heart", "angiosarcoma of heart (diagnosis)", "Hemangiosarcoma of heart (disorder)", "hemangiosarcoma of heart (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemangiosarcoma of heart", "shortest_name_length": 18}
{"curie": "MONDO:0100514", "names": ["hereditary ovarian cancer", "Hereditary Ovarian Cancer", "Familial Ovarian Carcinoma", "familiar ovarian carcinoma", "familial ovarian carcinoma", "hereditary ovarian carcinoma", "Hereditary Ovarian Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial ovarian carcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0033543", "names": ["CRSDS", "cone-rod synaptic disorder syndrome, congenital nonprogressive", "CONE-ROD SYNAPTIC DISORDER SYNDROME, CONGENITAL NONPROGRESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cone-rod synaptic disorder syndrome, congenital nonprogressive", "shortest_name_length": 5}
{"curie": "MONDO:0014909", "names": ["CILD34", "primary ciliary dyskinesia 34", "CILIARY DYSKINESIA, PRIMARY, 34", "ciliary dyskinesia, primary, 34", "DNAJB13 primary ciliary dyskinesia", "primary ciliary dyskinesia type 34", "ciliary dyskinesia, primary, type 34", "primary ciliary dyskinesia 34 without situs inversus", "ciliary dyskinesia, primary, 34, without situs inversus", "CILIARY DYSKINESIA, PRIMARY, 34, WITHOUT SITUS INVERSUS", "primary ciliary dyskinesia caused by mutation in DNAJB13"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia 34", "shortest_name_length": 6}
{"curie": "UMLS:C0279595", "names": ["non-T, non-B, cALLa positive adult ALL", "non-B, non-T, cALLa positive adult ALL", "adult ALL, non T, non B, cALLa positive", "ALL, adult non T, non B, cALLa positive", "adult ALL, non-T, non-B, cALLa positive", "non T, non B, adult ALL, cALLa positive", "cALLa positive, non-T, non-B, adult ALL", "ALL, adult non-T, non-B, cALLa positive", "cALLa positive, non T, non B, adult ALL", "ALL, non-T, non-B, cALLa positive, adult", "ALL, cALLa positive, non T, non B, adult", "ALL, non T, non B, cALLa positive, adult", "leukemia, cALLa positive, non-T, non-B, adult", "leukemia, ALL non T, non B, cALLa positive, adult", "Non-T Non-B CALLA Positive Acute Lymphoblastic Leukemia", "Non-T Non-B CALLA Positive Adult Acute Lymphoblastic Leukemia", "non B, non T, cALLa positive adult acute lymphocytic leukemia", "cALLa positive, non-T, non-B adult acute lymphocytic leukemia", "non-T, non-B, cALLa positive adult acute lymphocytic leukemia", "non T, non B, cALLa positive adult acute lymphocytic leukemia", "leukemia, adult acute lymphocytic non-T, non-B, cALLa positive", "acute lymphocytic leukemia, adult non-T, non-B, cALLa positive", "non-T, non-B, cALLa positive adult acute lymphoblastic leukemia", "acute lymphoblastic leukemia, adult non-T, non-B, cALLa positive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-T Non-B CALLA Positive Adult Acute Lymphoblastic Leukemia", "shortest_name_length": 38}
{"curie": "MONDO:0044098", "names": ["Ovarian Pregnancy", "ovarian pregnancy", "Ovarian pregnancy", "pregnancy ovarian", "PREGNANCY, OVARIAN", "Pregnancy, Ovarian", "Pregnancy, ovarian", "ovarian; pregnancy", "pregnancy; ovarian", "ovarian Pregnancies", "Ovarian Pregnancies", "Pregnancies, ovarian", "Pregnancies, Ovarian", "Ovarian pregnancy NOS", "ovary ectopic pregnancy", "ovarian ectopic pregnancy", "ectopic pregnancy of ovary", "Ovarian pregnancy (disorder)", "ovarian pregnancy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian ectopic pregnancy", "shortest_name_length": 17}
{"curie": "UMLS:C0919671", "names": ["subileus", "Subileus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subileus", "shortest_name_length": 8}
{"curie": "UMLS:C2217676", "names": ["Thyroid cancer stage I", "thyroid cancer stage I", "malignant tumor of thyroid stage I", "malignant neoplasm of thyroid stage I", "malignant neoplasm of thyroid stage I (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid cancer stage I", "shortest_name_length": 22}
{"curie": "MONDO:0018111", "names": ["idiopathic severe pneumococcemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic severe pneumococcemia", "shortest_name_length": 32}
{"curie": "UMLS:C1708980", "names": ["Mesenchymal Chondrosarcoma of Bone", "mesenchymal chondrosarcoma of bone", "Mesenchymal Chondrosarcoma of the Bone", "mesenchymal chondrosarcoma of bone (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mesenchymal chondrosarcoma of bone", "shortest_name_length": 34}
{"curie": "UMLS:C5401356", "names": ["OGA", "Oxyntic Gland Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oxyntic Gland Adenoma", "shortest_name_length": 3}
{"curie": "MONDO:0010909", "names": ["UVSS1", "UV-Sensitive Syndrome 1", "UV-sensitive syndrome 1", "UV-SENSITIVE SYNDROME 1", "ERCC6 UV-sensitive syndrome", "UV-sensitive syndrome type 1", "UV-sensitive syndrome caused by mutation in ERCC6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "UV-sensitive syndrome 1", "shortest_name_length": 5}
{"curie": "UMLS:C5575459", "names": ["IVLBCL", "Lung Intravascular Large B-Cell Lymphoma", "Pulmonary Intravascular Large B-Cell Lymphoma", "Intravascular Large B-Cell Lymphoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Intravascular Large B-Cell Lymphoma", "shortest_name_length": 6}
{"curie": "MONDO:0008379", "names": ["RP10", "Retinitis Pigmentosa 10", "RETINITIS PIGMENTOSA 10", "retinitis pigmentosa 10", "IMPDH1 retinitis pigmentosa", "retinitis pigmentosa type 10", "retinitis pigmentosa caused by mutation in IMPDH1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 10", "shortest_name_length": 4}
{"curie": "UMLS:C4725953", "names": ["Unresectable Gastrointestinal Stromal Tumor", "Unresectable Gastrointestinal Stromal Tumor (GIST)", "Unresectable Malignant Gastrointestinal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Malignant Gastrointestinal Stromal Tumor", "shortest_name_length": 43}
{"curie": "MONDO:0100025", "names": ["epilepsy of infancy with migrating focal seizures", "Epilepsy of infancy with migrating focal seizures", "Epilepsy of infancy with migrating focal seizures (disorder)", "epilepsy of infancy with migrating focal seizures (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy of infancy with migrating focal seizures", "shortest_name_length": 49}
{"curie": "UMLS:C5235951", "names": ["Unresectable Alveolar Soft Part Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Alveolar Soft Part Sarcoma", "shortest_name_length": 39}
{"curie": "UMLS:C1266107", "names": ["Sertoli-Leydig cell tumor, retiform, with heterologous elements", "Sertoli-Leydig cell tumour, retiform, with heterologous elements", "Sertoli-Leydig cell tumor, moderately differentiated, with heterologous elements", "Sertoli-Leydig cell tumour, moderately differentiated, with heterologous elements", "Sertoli-Leydig cell tumor, intermediate differentiation, with heterologous elements", "Sertoli-Leydig cell tumour, intermediate differentiation, with heterologous elements", "Moderately Differentiated Ovarian Sertoli-Leydig Cell Tumor, Variant with Heterologous Elements", "Intermediate Differentiated Ovarian Sertoli-Leydig Cell Tumor, Variant with Heterologous Elements", "Sertoli-Leydig cell tumor, intermediate differentiation, with heterologous elements (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sertoli-Leydig cell tumor, intermediate differentiation, with heterologous elements", "shortest_name_length": 63}
{"curie": "UMLS:C0338715", "names": ["depression drug-induced", "Drug-induced depression", "Drug-induced depressive state", "Depressive state induced by drugs", "Depressive disorder caused by drug", "Drug-induced organic affective syndrome", "Drug-induced depressive state (diagnosis)", "Depressive disorder caused by drug (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drug-induced depressive state", "shortest_name_length": 23}
{"curie": "MONDO:0003500", "names": ["squamous cell bile duct carcinoma", "bile duct squamous cell carcinoma", "Squamous Cell Bile Duct Carcinoma", "Bile duct squamous cell carcinoma", "Bile Duct Squamous Cell Carcinoma", "Squamous Cell Carcinoma of Bile Duct", "Squamous Cell Carcinoma of the Bile Duct", "Extrahepatic Bile Duct Squamous Cell Carcinoma", "extrahepatic bile duct squamous cell carcinoma", "squamous cell carcinoma of extrahepatic bile duct", "squamous cell carcinoma of the extrahepatic bile duct", "squamous cell carcinoma of extrahepatic bile duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "squamous cell bile duct carcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C5419044", "names": ["Adverse Drug Reaction to Systemic Antibiotic", "Adverse Drug Reaction to Systemic Antibiotics"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adverse Drug Reaction to Systemic Antibiotic", "shortest_name_length": 44}
{"curie": "UMLS:C2713367", "names": ["Severe Teratoid Abnormality", "Teratoid Abnormality, Severe", "Abnormality, Severe Teratoid", "Severe Teratoid Abnormalities", "Abnormalities, Severe Teratoid", "Teratoid Abnormalities, Severe"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abnormality, Severe Teratoid", "shortest_name_length": 27}
{"curie": "UMLS:C0919896", "names": ["Myeloblastoma", "Blastic Granulocytic Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Blastic Granulocytic Sarcoma", "shortest_name_length": 13}
{"curie": "UMLS:C5446940", "names": ["Breast Cellular Fibroadenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Cellular Fibroadenoma", "shortest_name_length": 28}
{"curie": "UMLS:C1880953", "names": ["Germ Cell Tumor (Antiquated)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Germ Cell Tumor (Antiquated)", "shortest_name_length": 28}
{"curie": "MONDO:0007554", "names": ["EBS-K", "EBS1B", "EB simplex", "Kobner disease", "generalized EBS", "Generalized EBS", "EBS, Generalized", "EBS, generalized", "Kabner's disease", "Generalized EBSs", "EBSs, Generalized", "EBS, generalized intermediate", "Koebner epidermolysis bullosa", "Epidermolysis Bullosa Simplex Kobner", "generalized EBS, non-Dowling-Meara type", "Generalized epidermolysis bullosa simplex", "Generalised epidermolysis bullosa simplex", "epidermolysis bullosa simplex, Köbner type", "epidermolysis bullosa simplex, Kobner type", "Epidermolysis Bullosa Simplex, Generalized", "epidermolysis bullosa simplex, generalized", "Epidermolysis bullosa simplex, Kobner type", "epidermolysis bullosa simplex Koebner type", "Epidermolysis bullosa simplex, Köbner type", "Epidermolysis Bullosa Simplex, Koebner Type", "epidermolysis bullosa simplex, Koebner type", "Epidermolysis bullosa simplex, Koebner type", "epidermolysis bullosa simplex generalized type", "EPIDERMOLYSIS BULLOSA SIMPLEX 1B, KOEBNER TYPE", "Generalized epidermolysis bullosa simplex (disorder)", "Autosomal dominant generalized EBS, intermediate form", "epidermolysis bullosa simplex, generalized intermediate", "epidermolysis bullosa simplex 1B, generalized intermediate", "EPIDERMOLYSIS BULLOSA SIMPLEX 1B, GENERALIZED INTERMEDIATE", "epidermolysis bullosa simplex, generalized non-Dowling-Meara", "generalized epidermolysis bullosa simplex, non-Dowling-Meara type", "Autosomal dominant generalized epidermolysis bullosa simplex, intermediate form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolysis bullosa simplex 1B, generalized intermediate", "shortest_name_length": 5}
{"curie": "UMLS:C0543800", "names": ["idiopathic hypercalciuria", "Idiopathic hypercalciuria", "hypercalciuria; idiopathic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Idiopathic hypercalciuria", "shortest_name_length": 25}
{"curie": "MONDO:0100043", "names": ["epidermodysplasia verruciformis, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermodysplasia verruciformis, susceptibility to", "shortest_name_length": 50}
{"curie": "MONDO:0008782", "names": ["AMYOTROPHIC LATERAL SCLEROSIS WITH POLYGLUCOSAN BODIES", "amyotrophic lateral sclerosis with polyglucosan bodies", "Amyotrophic Lateral Sclerosis With Polyglucosan Bodies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyotrophic lateral sclerosis with polyglucosan bodies", "shortest_name_length": 54}
{"curie": "MONDO:0010730", "names": ["Xcid", "CIDX", "immunodeficiency 6", "combined immunodeficiency, X-linked", "X-Linked Combined Immunodeficiency Diseases", "combined immunodeficiency, X-linked, moderate, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined immunodeficiency, X-linked", "shortest_name_length": 4}
{"curie": "UMLS:C5557350", "names": ["Vulvar Phyllodes Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Phyllodes Tumor", "shortest_name_length": 22}
{"curie": "UMLS:C0220597", "names": ["Adult HD", "adult HD", "HD, adult", "Hodgkin Lymphoma", "adult Hodgkin disease", "adult Hodgkin lymphoma", "adult Hodgkins disease", "Adult Hodgkin Lymphoma", "adult hodgkin's disease", "adult Hodgkins lymphoma", "adult Hodgkin's disease", "Adult Hodgkin's Disease", "Hodgkin Lymphoma, Adult", "Hodgkin's disease, adult", "adult hodgkin's lymphoma", "adult Hodgkin's lymphoma", "adults disease hodgkin's", "Adult Hodgkin's Lymphoma", "Hodgkin's lymphoma, adult", "lymphoma, Hodgkin's, adult", "Lymphoma, Hodgkin lymphoma, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Hodgkin Lymphoma", "shortest_name_length": 8}
{"curie": "MONDO:0008632", "names": ["Aquagenic Urticaria", "Aquagenic urticaria", "Urticaria aquagenic", "aquagenic urticaria", "Aquagenic Urticarias", "URTICARIA, AQUAGENIC", "urticaria, aquagenic", "Urticaria, Aquagenic", "Aquagenic urticaria (disorder)", "[OBSOLETE] Urticaria, Aquagenic", "Aquagenic angio-edema-urticaria", "Aquagenic angio-oedema-urticaria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urticaria, aquagenic", "shortest_name_length": 19}
{"curie": "UMLS:C2981634", "names": ["Stage II Hilar Cholangiocarcinoma", "Stage II Hilar Cholangiocarcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Hilar Cholangiocarcinoma AJCC v7", "shortest_name_length": 33}
{"curie": "MONDO:0005040", "names": ["Germ cell tumor", "GERM CELL TUMOR", "Germ Cell Tumor", "germ cell tumor", "germ cell tumour", "Tumor, Germ Cell", "Germ Cell Tumors", "Germ cell tumour", "germ cell cancer", "germ cell tumors", "germ cells tumors", "cell germ tumours", "Tumors, Germ Cell", "cells germ tumors", "Germ Cell Neoplasm", "Tumor of Germ Cell", "tumor of germ cell", "Germ cell neoplasm", "germ cell neoplasm", "germ cell neoplasms", "Germ Cell Neoplasms", "GERM CELL NEOPLASMS", "Germ cell tumor, NOS", "Neoplasms, Germ Cell", "Neoplasm of Germ Cell", "Germ cell tumour, NOS", "neoplasm of germ cell", "Tumor of the Germ Cell", "tumor of the germ cell", "neoplasm of the germ cell", "Neoplasm of the Germ Cell", "Germ cell tumor (disorder)", "germ cell tumor (diagnosis)", "germ cell and embryonal cancer", "malignant tumor of the germ cell", "germ cell and embryonal neoplasm", "Germ Cell and Embryonic Neoplasms", "Germ Cell and Embryonal Neoplasms", "Neoplasms, Germ Cell and Embryonic", "Neoplasms, Germ Cell and Embryonal", "Germ cell neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "germ cell tumor", "shortest_name_length": 15}
{"curie": "UMLS:C5206435", "names": ["Stage I Cervical Cancer FIGO 2018", "Stage I Cervical Carcinoma FIGO 2018"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Cervical Cancer FIGO 2018", "shortest_name_length": 33}
{"curie": "MONDO:0024386", "names": ["clear cell carcinoma of the lung", "Clear Cell Lung Carcinoma, Large Cell Type", "clear cell lung carcinoma, large cell type", "clear cell carcinoma of lung, large cell type", "Lung Large Cell Carcinoma, Clear Cell Variant", "large cell lung carcinoma, clear cell variant", "Large Cell Lung Carcinoma, Clear Cell Variant", "Clear Cell Carcinoma of Lung, Large Cell Type", "Clear Cell Carcinoma of the Lung, Large Cell Type", "clear cell carcinoma of the lung, large cell type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "large cell lung carcinoma, clear cell variant", "shortest_name_length": 32}
{"curie": "MONDO:0018332", "names": ["MADD, severe neonatal type", "MAD deficiency, severe neonatal type", "glutaric aciduria type 2, severe neonatal type", "multiple acyl-CoA dehydrogenase deficiency, severe neonatal type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple acyl-CoA dehydrogenase deficiency, severe neonatal type", "shortest_name_length": 26}
{"curie": "UMLS:C1707445", "names": ["Columnar Cell Change with Atypia", "Columnar Cell Change of Breast with Atypia", "Columnar Cell Change of the Breast with Atypia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Columnar Cell Change of the Breast with Atypia", "shortest_name_length": 32}
{"curie": "UMLS:C1336162", "names": ["Stage IIA Large Cell Lung Cancer", "Stage IIA Large Cell Lung Carcinoma", "Stage IIA Large Cell Carcinoma of Lung", "Stage IIA Large Cell Carcinoma of the Lung", "Stage IIA Lung Large Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Lung Large Cell Carcinoma AJCC v7", "shortest_name_length": 32}
{"curie": "MONDO:0008400", "names": ["calculus; Wharton", "Wharton; calculus", "Sialodocholithiasis", "duct salivary stone", "sialodocholithiasis", "salivary duct stone", "Salivary Duct Stone", "Stone, Salivary Duct", "Salivary Duct Stones", "parotid duct calculi", "salivary duct stones", "Parotid Duct Calculi", "Duct Stone, Salivary", "PAROTID DUCT CALCULI", "SALIVARY DUCT CALCULI", "Salivary Duct Calculi", "Stones, Salivary Duct", "Duct Stones, Salivary", "calculi duct salivary", "salivary duct calculi", "Stone of salivary duct", "Sialolithiases, Ductal", "Salivary duct calculus", "Sialolithiasis, Ductal", "Calculi, Salivary Duct", "Duct Calculi, Salivary", "Calculus salivary duct", "Salivary Duct Calculus", "salivary duct; calculus", "Duct Calculus, Salivary", "Calculus, Salivary Duct", "calculus of salivary duct", "Calculus of salivary duct", "Calculus in salivary duct", "Submandibular Duct Calculi", "submandibular duct calculi", "SUBMANDIBULAR DUCT CALCULI", "calculus; submandibular duct", "Sialodocholithiasis (disorder)", "calculus of salivary duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "salivary duct calculi", "shortest_name_length": 17}
{"curie": "UMLS:C4525208", "names": ["IVB", "Stage IVB Hepatocellular Cancer", "Stage IVB Liver Cell Carcinoma AJCC v8", "Stage IVB Hepatocellular Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Hepatocellular Carcinoma AJCC v8", "shortest_name_length": 3}
{"curie": "UMLS:C1519696", "names": ["Tumor of the Thecoma/Fibroma Group"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tumor of the Thecoma/Fibroma Group", "shortest_name_length": 34}
{"curie": "UMLS:C5447286", "names": ["Localized Prostate Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized Prostate Carcinoma", "shortest_name_length": 28}
{"curie": "UMLS:C4721925", "names": ["Stage IC Uterine Sarcoma", "stage IC uterine sarcoma", "Stage IC Uterine Sarcoma AJCC v7", "stage IC uterine sarcoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IC Uterine Sarcoma AJCC v7", "shortest_name_length": 24}
{"curie": "UMLS:C0235895", "names": ["implant complication", "implant complications", "complications implants", "Complication;implant(s)", "Complication of implant", "implantation complication", "Implantation complication", "complication with implant", "IMPLANTATION COMPLICATION", "Complication of implant (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Complication of implant", "shortest_name_length": 20}
{"curie": "MONDO:0005135", "names": ["parasitism", "Parasitosis", "Infestation", "infestation", "parasitemia", "parasitosis", "Parasitosis, NOS", "parasitic disease", "Parasitic disease", "Parasitic Disease", "Disease;parasitic", "Disease, Parasitic", "Parasite Infection", "Parasitic diseases", "disease, parasitic", "parasitic diseases", "PARASITIC DISEASES", "Parasitic Diseases", "parasitic; disease", "Parasite Infections", "Infection, Parasite", "Infection parasitic", "INFECTION PARASITIC", "parasitic infection", "diseases, parasitic", "Diseases, Parasitic", "PARASITIC INFECTION", "Parasitic infection", "Parasitic Infection", "Parasitic Disorders", "parasite infestation", "infection; parasitic", "parasitic; infection", "Parasite infestation", "Infections, Parasite", "Infection, Parasitic", "Parasitic Infections", "Parasitic disease NOS", "parasite; infestation", "Ectoparasitic disease", "ectoparasitic disease", "Infections, Parasitic", "Parasitic Infestation", "infestation; parasite", "PARASITIC INFESTATION", "Parasitic disease, NOS", "Parasitic infection NOS", "Parasitic infection, NOS", "Parasite infestation, NOS", "Disease caused by parasite", "disease caused by parasite", "disease caused by a parasite", "parasitic infectious disease", "Parasitic infectious disease", "PARASITIC INFECTION INFECTIOUS", "parasitic infection (diagnosis)", "Disease caused by parasite, NOS", "Parasitic infectious disease, NOS", "Disease caused by parasite (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parasitic infectious disease", "shortest_name_length": 10}
{"curie": "MONDO:0024985", "names": ["sheep disease", "Ovine Disease", "Ovine disease", "Sheep Disease", "Sheep Diseases", "Ovine Diseases", "disease, Ovine", "Disease, Sheep", "disease, sheep", "Ovine diseases", "Disease, Ovine", "diseases, Ovine", "Sheep--Diseases", "diseases, sheep", "Diseases, Ovine", "Diseases, Sheep"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sheep disease", "shortest_name_length": 13}
{"curie": "MONDO:0009607", "names": ["MAT Deficiency", "MAT deficiency", "MAT I/III Deficiency", "MAT I/III deficiency", "Mat I/III deficiency", "isolated persistent hypermethioninemia", "Isolated Persistent Hypermethioninemia", "hypermethioninemia, isolated persistent", "Hypermethioninemia, Isolated Persistent", "Methionine Adenosyltransferase Deficiency", "methionine adenosyltransferase deficiency", "methionine adenosyltransferase I/III deficiency", "methionine adenosyltransferase deficiency, autosomal recessive", "brain demyelination due to methionine adenosyltransferase deficiency", "hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase I/III deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "methionine adenosyltransferase deficiency", "shortest_name_length": 14}
{"curie": "MONDO:0022453", "names": ["angiomyomatous hamartoma", "Angiomyomatous hamartoma", "Angiomyomatous hamartoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angiomyomatous hamartoma", "shortest_name_length": 24}
{"curie": "UMLS:C5556806", "names": ["Refractory Primary Cutaneous Anaplastic Large Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Primary Cutaneous Anaplastic Large Cell Lymphoma", "shortest_name_length": 59}
{"curie": "MONDO:0005802", "names": ["Hymenolepis", "Hymenolepiosis", "hymenolepiasis", "Hymenolepiases", "Dwarf tapeworm", "Hymenolepiasis", "dwarf tapeworms", "hymenolepiasis nana", "HYMENOLEPIASIS NANA", "Hymenolepis infection", "Hymenolepis Infection", "Hymenolepis Infections", "Infection, Hymenolepis", "Hymenolepsis infection", "Infections, Hymenolepis", "dwarf tapeworm infection", "Dwarf tapeworm infection", "dwarf tapeworm; infection", "Hymenolepiasis (disorder)", "hyemolepis nana infection", "hymenolepis infection nana", "Hymenolepis nana infection", "hymenolepiasis (diagnosis)", "infestation; dwarf tapeworm", "Hymenolepsis nana infection", "dwarf tapeworm; infestation", "infestation; tapeworm, dwarf", "Hymenolepis infectious disease", "Hymenolepis nana infection (disorder)", "Hymenolepis nana infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hymenolepiasis", "shortest_name_length": 11}
{"curie": "MONDO:0054801", "names": ["ECYT6", "erythrocytosis 6", "familial erythrocytosis 6", "ERYTHROCYTOSIS, FAMILIAL, 6", "erythrocytosis, FAMILIAL, 6", "erythrocytosis, familial, 6", "beta-globin type polycythemia", "polycythemia, Beta-globin type", "POLYCYTHEMIA, BETA-GLOBIN TYPE", "beta-globin type erythrocytosis", "erythrocytosis, Beta-globin type", "ERYTHROCYTOSIS, BETA-GLOBIN TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythrocytosis, familial, 6", "shortest_name_length": 5}
{"curie": "UMLS:C1336334", "names": ["stage IVA endometrial cancer", "stage IVA uterine corpus cancer", "stage IVA endometrial carcinoma", "Stage IVA Uterine Corpus Cancer", "stage IVA uterine corpus cancer AJCC v7", "Stage IVA Uterine Corpus Cancer AJCC v7", "Stage IVA Uterine (including Endometrial) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Uterine Corpus Cancer AJCC v7", "shortest_name_length": 28}
{"curie": "UMLS:C0855161", "names": ["Stage I Extragonadal Mixed Germ Cell Tumor", "Extragonadal primary germ cell tumor mixed stage I", "Stage I Extragonadal Primary Mixed Germ Cell Tumor", "Stage I Extragonadal Primary Germ Cell Tumor Mixed", "Extragonadal primary germ cell tumour mixed stage I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extragonadal primary germ cell tumor mixed stage I", "shortest_name_length": 42}
{"curie": "MONDO:0013935", "names": ["USH1J", "CIB2 Usher syndrome", "Usher syndrome type Ij", "Usher syndrome type 1J", "Usher syndrome type IJ", "USHER SYNDROME, TYPE IJ", "Usher syndrome, type 1J", "USHER syndrome, type Ij", "Usher syndrome caused by mutation in CIB2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Usher syndrome type 1J", "shortest_name_length": 5}
{"curie": "UMLS:C0029104", "names": ["opioid withdrawal", "OPIOID WITHDRAWAL", "Opioid withdrawal", "withdrawal narcotic", "narcotic withdrawal", "Narcotic withdrawal", "narcotics withdrawal", "opioids; withdrawal state", "withdrawal state; opioids", "Opioid withdrawal syndrome", "opioid withdrawal (diagnosis)", "Drug withdrawal syndrome to opium", "Opioid withdrawal syndrome (disorder)", "Mental and behavioral disorders due to use of opioids, withdrawal state", "Mental and behavioural disorders due to use of opioids, withdrawal state"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Opioid withdrawal", "shortest_name_length": 17}
{"curie": "MONDO:0009872", "names": ["PTD", "BJS", "PTND", "Björnstad syndrome", "BJörnstad syndrome", "Bjornstad syndrome", "BJORNSTAD SYNDROME", "Bjornstad's syndrome", "Pili torti-deafness syndrome", "PILI TORTI AND NERVE DEAFNESS", "Pili torti and nerve deafness", "pili torti and nerve deafness", "pili torti-sensorineural hearing loss", "Pili torti-sensorineural hearing loss", "Deafness and pili torti, Bjornstad type", "deafness and pili torti, Bjornstad type", "Pili torti-deafness syndrome (disorder)", "deafness-pili torti-hypogonadism syndrome", "Deafness-pili torti-hypogonadism syndrome", "Hearing loss-pili torti-hypogonadism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bjornstad syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0010545", "names": ["NHS", "Nance-Horan syndrome", "NANCE-HORAN SYNDROME", "Cataract-Dental Syndrome", "CATARACT-DENTAL SYNDROME", "cataract dental syndrome", "cataract-dental syndrome", "Nance-Horan syndrome (NHS)", "Mesiodens-Cataract Syndrome", "mesiodens-cataract syndrome", "Mesiodens-cataract syndrome", "Mesiodens cataract syndrome", "MESIODENS-CATARACT SYNDROME", "Nance-Horan syndrome (disorder)", "X-linked cataract-dental syndrome", "nance-horan syndrome, X-linked dominant", "X-linked cataract with hutchinsonian teeth", "cataract X-linked with Hutchinsonian teeth", "CATARACT, X-LINKED, WITH HUTCHINSONIAN TEETH", "cataract, X-linked, with Hutchinsonian teeth", "Cataract, X-linked, with Hutchinsonian Teeth", "brachymetacarpalia-cataract-mesiodens syndrome", "X-linked congenital cataracts-microcornea syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nance-Horan syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C5418872", "names": ["Locally Advanced Colon Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Colon Carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0003479", "names": ["toxic pneumonitis", "Toxic pneumonitis", "chemical pneumonia", "Pneumonia, chemical", "chemicals pneumonia", "chemical pneumonitis", "pneumonitis chemical", "CHEMICAL PNEUMONITIS", "Chemical Pneumonitis", "Chemical pneumonitis", "PNEUMONITIS CHEMICAL", "Pneumonitis chemical", "pneumonitis; chemicals", "chemicals; pneumonitis", "Toxic pneumonitis (disorder)", "acute chemical pulmonary edema", "Chemical pneumonitis (diagnosis)", "acute chemical fume pulmonary edema", "Unspecified respiratory conditions due to fumes and vapors"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "toxic pneumonitis", "shortest_name_length": 17}
{"curie": "MONDO:0019537", "names": ["Hb-D disease", "Hb D-disease", "Homozygous for Hb D", "Hemoglobin D Disease", "Hemoglobin D disease", "hemoglobin D disease", "Haemoglobin D disease", "Hemoglobin D-D disease", "Haemoglobin D-D disease", "Hemoglobin D disease (disorder)", "Sickle Cell-Hemoglobin D Disease", "hemoglobin D disease (diagnosis)", "disease (or disorder); hemoglobin or Hb, D (Hb-D)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemoglobin D disease", "shortest_name_length": 12}
{"curie": "MONDO:0005364", "names": ["Graves", "Basedow", "Flajani", "GRAVE DISEASE", "parry disease", "Morbus Basedow", "Graves disease", "Disease;Graves", "GRAVES DISEASE", "graves disease", "Graves Disease", "disease graves", "BASEDOW DISEASE", "Graves' Disease", "Basedow disease", "graves' disease", "DISEASE GRAVES'", "Grave's disease", "grave's disease", "FLAJANI DISEASE", "basedow disease", "Basedow Disease", "Graves' disease", "Disease, Graves", "diseases graves", "GRAVES' DISEASE", "basedows disease", "Disease, Graves'", "Disease;Basedows", "Basedows disease", "Basedows Disease", "Disease, Basedow", "Basedow's disease", "basedow's disease", "Basedow's Disease", "Disease, Basedow's", "Exophthalmic goitre", "GOITER EXOPHTHALMIC", "Goitre exophthalmic", "EXOPHTHALMIC GOITRE", "Exophthalmic Goiter", "Exophthalmic goiter", "exophthalmic goiter", "Goiter exophthalmic", "EXOPHTHALMIC GOITER", "exophthalmic; goiter", "GOITER, EXOPHTHALMIC", "Goiter, Exophthalmic", "Exophthalmic Goiters", "struma; exophthalmic", "Goiters, Exophthalmic", "Graves-Basedow disease", "Graves' hyperthyroidism", "Autoimmune hyperthyroidism", "Graves' disease (disorder)", "Graves' disease (diagnosis)", "HYPERTHYROIDISM, AUTOIMMUNE", "Hyperthyroidism, Autoimmune", "HYPERTHYROIDISM GRAVES DISEASE", "hyperthyroidism graves disease", "goiter; exophthalmos (etiology)", "exophthalmos; goiter (etiology)", "HYPERTHYROIDISM <GRAVES DISEASE>", "Graves' Disease - hyperthyroidism", "Graves' disease with exophthalmos", "exophthalmos; goiter (manifestation)", "goiter; exophthalmos (manifestation)", "Toxic diffuse goiter with exophthalmos", "Toxic diffuse goitre with exophthalmos", "Graves' disease (diffuse toxic goiter)", "Exophthalmos due to toxic diffuse goitre", "Exophthalmos due to toxic diffuse goiter", "Graves' disease due to toxic diffuse goitre", "Graves' disease due to toxic diffuse goiter", "Exophthalmos due to toxic diffuse goiter (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Graves disease", "shortest_name_length": 6}
{"curie": "MONDO:0002138", "names": ["eyelid allergic contact dermatitis", "allergic contact dermatitis of eyelid", "Allergic contact dermatitis of eyelid", "dermatitis of eyelid contact, allergic", "Contact and allergic dermatitis of eyelid", "contact and allergic dermatitis of eyelid", "Allergic contact dermatitis of eyelid (disorder)", "allergic contact dermatitis of eyelid (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "allergic contact dermatitis of eyelid", "shortest_name_length": 34}
{"curie": "MONDO:0012651", "names": ["SPAX2", "SPG58", "spastic ataxia 2", "KIF1C spastic ataxia", "spastic ataxia type 2", "Autosomal spastic ataxia type 2", "Autosomal Recessive Spastic Ataxia-2", "Autosomal Spastic Paraplegia Type 58", "Autosomal spastic paraplegia type 58", "SPASTIC ATAXIA 2, AUTOSOMAL RECESSIVE", "spastic ataxia 2, autosomal recessive", "Ataxia, Spastic, 2, Autosomal Recessive", "autosomal recessive spastic ataxia type 2", "spastic ataxia caused by mutation in KIF1C", "autosomal recessive spastic paraplegia type 58"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic ataxia 2", "shortest_name_length": 5}
{"curie": "MONDO:0001614", "names": ["intra-abdominal lymph node mast cell malignancy", "mast cell malignancy of lymph nodes intra-abdominal", "mast cell malignancy of intra-abdominal lymph nodes", "Mast cell malignancy of intra-abdominal lymph nodes", "malignant mastocytosis of intra-abdominal lymph nodes", "Malignant mast cell tumors, intra-abdominal lymph nodes", "Mast cell malignancy of intra-abdominal lymph nodes (diagnosis)", "malignant mast cell tumors involving intra-abdominal lymph nodes", "Malignant mast cell tumors involving intra-abdominal lymph nodes", "malignant mastocytosis of intra-abdominal lymph nodes (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intra-abdominal lymph node mast cell malignancy", "shortest_name_length": 47}
{"curie": "MONDO:0000878", "names": ["RETINITIS CMV", "cmv retinitis", "retinitis cmv", "CMV retinitis", "cytomegalovirus retinitis", "Cytomegalovirus retinitis", "RETINITIS CYTOMEGALOVIRUS", "Cytomegaloviral Retinitis", "Cytomegalovirus Retinitis", "Cytomegaloviral retinitis", "Retinitis, Cytomegaloviral", "Retinitis, Cytomegalovirus", "CMV - Cytomegalovirus retinitis", "Cytomegalovirus caused retinitis", "Cytomegaloviral retinitis (disorder)", "cytomegalovirus retinitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cytomegalovirus retinitis", "shortest_name_length": 13}
{"curie": "MONDO:0004291", "names": ["subglottis epidermoid carcinoma", "Subglottis Epidermoid Carcinoma", "Subglottic Epidermoid Carcinoma", "subglottic epidermoid carcinoma", "subglottic squamous cell carcinoma", "Subglottis Squamous Cell Carcinoma", "Subglottic Squamous Cell Carcinoma", "epidermoid carcinoma of subglottis", "Epidermoid Carcinoma of Subglottis", "subglottis squamous cell carcinoma", "Squamous Cell Carcinoma of Subglottis", "squamous cell carcinoma of subglottis", "Epidermoid Carcinoma of the Subglottis", "epidermoid carcinoma of the subglottis", "Epidermoid carcinoma of the Subglottis", "squamous cell carcinoma of the subglottis", "Squamous Cell Carcinoma of the Subglottis", "squamous cell carcinoma of subglottis (diagnosis)", "malignant subglottis neoplasm carcinoma squamous cell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subglottis squamous cell carcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C4552927", "names": ["IB2", "Stage IB2 Cervical Cancer", "Stage IB2 Cervical Cancer AJCC v8", "Stage IB2 Cervical Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB2 Cervical Cancer AJCC v8", "shortest_name_length": 3}
{"curie": "UMLS:C4744983", "names": ["Metastatic Gastric Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Gastric Neuroendocrine Carcinoma", "shortest_name_length": 43}
{"curie": "UMLS:C1335516", "names": ["Prostate Non-Hodgkin Lymphoma", "Prostate Non-Hodgkin's Lymphoma", "Non-Hodgkin lymphoma of prostate", "Non-Hodgkin's Lymphoma of Prostate", "Non-Hodgkin's lymphoma of prostate", "Non-Hodgkin's Lymphoma of the Prostate", "Primary Prostate Non-Hodgkin's Lymphoma", "Non-Hodgkin's lymphoma of prostate (disorder)", "Non-Hodgkin's lymphoma of prostate (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Hodgkin's lymphoma of prostate", "shortest_name_length": 29}
{"curie": "MONDO:0700179", "names": ["Feline Osteosarcoma", "feline osteosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "feline osteosarcoma", "shortest_name_length": 19}
{"curie": "UMLS:C0265072", "names": ["IVC syndrome", "ivc obstruction", "IVC obstruction", "Caudal vena cava syndrome", "inferior vena cava syndrome", "VENA CAVA INFERIOR SYNDROME", "Inferior vena cava syndrome", "Inferior vena caval syndrome", "VENA CAVA INFERIOR OBSTRUCTION", "Inferior vena cava obstruction", "inferior vena cava obstruction", "Inferior vena caval obstruction", "VENA CAVA OBSTRUCTION, INFERIOR", "obstruction of inferior vena cava", "IVC - Inferior vena cava obstruction", "Inferior vena cava syndrome (disorder)", "inferior vena cava syndrome (diagnosis)", "VENA CAVA, INFERIOR, OBSTRUCTION SYNDROME", "obstruction of inferior vena cava (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Inferior vena cava syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0021253", "names": ["Gallbladder Tumor", "gallbladder tumor", "Gallbladder tumor", "gallbladder tumors", "Gallbladder tumour", "gallbladder tumour", "gall bladder tumor", "Gallbladder Neoplasm", "Tumor of gallbladder", "Gallbladder neoplasm", "tumor of gallbladder", "gallbladder neoplasm", "Tumor of Gallbladder", "Gallbladder Neoplasms", "gall bladder neoplasm", "Neoplasm, Gallbladder", "tumor of gall bladder", "gallbladder neoplasms", "Tumour of gallbladder", "Neoplasms, Gallbladder", "Neoplasm of Gallbladder", "neoplasm of gallbladder", "Neoplasm of gallbladder", "Tumor of the gallbladder", "neoplasm of gall bladder", "tumor of the gallbladder", "Tumor of the Gallbladder", "neoplasm of the gallbladder", "Neoplasm of the Gallbladder", "Neoplasm of the gallbladder", "Neoplasia of the gallbladder", "gall bladder neoplasm (disease)", "Neoplasm of gallbladder (disorder)", "neoplasm of gallbladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gallbladder neoplasm", "shortest_name_length": 17}
{"curie": "MONDO:0016093", "names": ["ovarian tum. of low malig. poten.", "Ovarian tum. of low malig. poten.", "ovarian borderline malignant tumor", "Borderline ovarian epithelial tumor", "borderline ovarian epithelial tumor", "Borderline Ovarian Epithelial Tumor", "Borderline ovarian epithelial tumour", "borderline epithelial tumor of ovary", "Borderline Epithelial Tumor of Ovary", "Borderline epithelial tumor of ovary", "Borderline epithelial tumour of ovary", "Ovarian low malignant potential tumor", "low malignant potential ovarian tumor", "Low Malignant Potential Ovarian Tumor", "ovarian low malignant potential tumor", "Borderline Ovarian Epithelial Neoplasm", "ovarian neoplasm epithelial borderline", "Ovarian low malignant potential tumour", "borderline ovarian epithelial neoplasm", "Borderline Epithelial Neoplasm of Ovary", "Borderline epithelial neoplasm of ovary", "borderline epithelial neoplasm of ovary", "ovarian tumor of low malignant potential", "Borderline Epithelial Tumor of the Ovary", "borderline epithelial tumor of the ovary", "Ovarian tumor of low malignant potential", "Ovarian tumors of low malignant potential", "ovarian tumors of low malignant potential", "neoplasm of borderline malignancy of ovary", "borderline epithelial neoplasm of the ovary", "Borderline Epithelial Neoplasm of the Ovary", "Epithelial Ovarian Tumor of Borderline Malignancy", "epithelial ovarian tumor of borderline malignancy", "Borderline epithelial neoplasm of ovary (disorder)", "epithelial tumor of ovary of borderline malignancy", "Epithelial Tumor of Ovary of Borderline Malignancy", "borderline ovarian surface epithelial-stromal tumor", "Borderline Ovarian Surface Epithelial-Stromal Tumor", "borderline epithelial neoplasm of ovary (diagnosis)", "epithelial ovarian neoplasm of borderline malignancy", "Epithelial Ovarian Neoplasm of Borderline Malignancy", "epithelial neoplasm of ovary of borderline malignancy", "Epithelial Neoplasm of Ovary of Borderline Malignancy", "epithelial tumor of the ovary of borderline malignancy", "neoplasm of borderline malignancy of ovary (diagnosis)", "Epithelial Tumor of the Ovary of Borderline Malignancy", "Epithelial Neoplasm of the Ovary of Borderline Malignancy", "epithelial neoplasm of the ovary of borderline malignancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "borderline epithelial tumor of ovary", "shortest_name_length": 33}
{"curie": "MONDO:0020513", "names": ["spermatocytoma", "Spermatocytoma", "Spermatocytic Tumor", "Spermatocytic Seminoma", "SPERMATOCYTIC SEMINOMA", "Spermatocytic seminoma", "spermatocytic seminoma", "Testicular Spermatocytic Tumor", "Testicular Spermatocytic Seminoma", "testicular spermatocytic seminoma", "Spermatocytic seminoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatocytic seminoma", "shortest_name_length": 14}
{"curie": "MONDO:0019992", "names": ["Albright syndrome 1", "pseudohypoparathyroidism", "MARTIN-ALBRIGHT SYNDROME", "Pseudohypoparathyroidism", "PSEUDOHYPOPARATHYROIDISM", "pseudo-hypoparathyroidism", "seabright bantam syndrome", "pseudohypoparathyroidisms", "Seabright Bantam syndrome", "SEABRIGHT-BANTAM SYNDROME", "Pseudo-hypoparathyroidism", "pseudo hypoparathyroidism", "Pseudohypoparathyroidisms", "Fuller Albright syndrome 1", "Pseudohypoparathyroidism, NOS", "PHP - Pseudohypoparathyroidism", "pseudopseudohypoparathyroidism", "Familial pseudohypoparathyroidism", "pseudohypoparathyroidism syndrome", "Albright hereditary osteodystrophy", "Pseudohypoparathyroidism (disorder)", "Constitutional chronic hypocalcemia", "pseudohypoparathyroidism (PHP, PHPT)", "Constitutional chronic hypocalcaemia", "pseudo hypoparathyroidism (diagnosis)", "Albright hereditary osteodystrophy, NOS", "Albright hereditary osteodystrophy (AHO)", "AHO - Albright hereditary osteodystrophy", "Parathyroid hormone resistant hypoparathyroidism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudohypoparathyroidism", "shortest_name_length": 19}
{"curie": "UMLS:C4683009", "names": ["Eyelid Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eyelid Carcinoma by AJCC v8 Stage", "shortest_name_length": 33}
{"curie": "MONDO:0100056", "names": ["EIAn", "exercise-induced anaphylaxis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exercise-induced anaphylaxis", "shortest_name_length": 4}
{"curie": "MONDO:0019286", "names": ["sebaceous gland anomaly", "sebaceous gland epidermal appendage anomaly", "epidermal appendage anomaly of sebaceous gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sebaceous gland anomaly", "shortest_name_length": 23}
{"curie": "MONDO:0002959", "names": ["Radiculopathy", "pinched nerve", "RADICULOPATHY", "radiculopathy", "radiculopathies", "Radiculopathies", "Radiculopathy NOS", "Radiculopathy, NOS", "Radicular Syndrome", "radicular syndrome", "Radicular syndrome", "Nerve Root Disorder", "Nerve root disorder", "syndrome; radicular", "radicular; syndrome", "nerve root disorder", "Nerve Root Disorders", "neuropathy; radicular", "radicular; neuropathic", "Nerve root disorder, NOS", "radiculopathy (diagnosis)", "Spinal nerve root disorder NOS", "Nerve root disorder (disorder)", "Radiculopathy, site unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radiculopathy", "shortest_name_length": 13}
{"curie": "UMLS:C4331339", "names": ["Stage IVA Nasopharyngeal Throat Cancer", "Stage IVA Nasopharyngeal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Nasopharyngeal Carcinoma AJCC v8", "shortest_name_length": 38}
{"curie": "MONDO:0007430", "names": ["Talon cusp", "Talon cusps", "dens evaginatus", "DENS EVAGINATUS", "Dens evaginatus", "Evaginated odontome", "Talon cusp (disorder)", "Dens evaginatus (disorder)", "dens evaginatus (diagnosis)", "Evagination of cusp of tooth", "Extra cusp on inside of front tooth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dens evaginatus", "shortest_name_length": 10}
{"curie": "UMLS:C4725675", "names": ["Refractory Bladder Cancer", "Refractory Bladder Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Bladder Carcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0032852", "names": ["MSCD", "MYOCOZ", "congenital myopathy 8", "Multiple Structured Core Disease", "MULTIPLE STRUCTURED CORE DISEASE", "myopathy, congenital with structured cores and z-line abnormalities", "MYOPATHY, CONGENITAL, WITH STRUCTURED CORES AND Z-LINE ABNORMALITIES", "myopathy, congenital, with structured cores and z-line abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy, congenital, with structured cores and z-line abnormalities", "shortest_name_length": 4}
{"curie": "MONDO:0011838", "names": ["VASTERBOTTEN DYSTROPHY", "Vasterbotten dystrophy", "Västerbotten dystrophy", "Vasterbotten Dystrophy", "VC$sterbotten dystrophy", "Bothnia retinal dystrophy", "BOTHNIA RETINAL DYSTROPHY", "Bothnia Retinal Dystrophy", "Bothnia retinal dystrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bothnia retinal dystrophy", "shortest_name_length": 22}
{"curie": "MONDO:0008053", "names": ["MYP2", "Myopia 2", "MYOPIA 2, AUTOSOMAL DOMINANT", "myopia 2, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopia 2, autosomal dominant", "shortest_name_length": 4}
{"curie": "MONDO:0009841", "names": ["peho", "PEHO", "PEHO SYNDROME", "PEHO syndrome", "peho syndrome", "peho-like syndrome", "Infantile cerebellooptic atrophy", "infantile Cerebellooptic atrophy", "INFANTILE CEREBELLOOPTIC ATROPHY", "infantile cerebello-optic atrophy", "progressive encephalopathy-optic atrophy syndrome", "Progressive encephalopathy-optic atrophy syndrome", "progressive encephalopathy-edema-hypsarrhythmia-optic atrophy syndrome", "progressive encephalopathy with edema, hypsarrhythmia and optic atrophy", "Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy", "PROGRESSIVE ENCEPHALOPATHY WITH EDEMA, HYPSARRHYTHMIA, AND OPTIC ATROPHY", "progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy", "Progressive Encephalopathy with edema, Hypsarrhythmia, and Optic atrophy", "progressive encephalopathy-edema-hypsarrhythmia-optic atrophy (PEHO) syndrome", "Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome", "Progressive encephalopathy with oedema, hypsarrhythmia and optic atrophy syndrome", "progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy syndrome", "PEHO (progressive encephalopathy with edema, hypsarrhythmia and optic atrophy) syndrome", "PEHO (progressive encephalopathy with oedema, hypsarrhythmia and optic atrophy) syndrome", "Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome (disorder)", "progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PEHO syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0010349", "names": ["ODG2", "POF4", "Ovarian Dysgenesis 2", "ovarian dysgenesis 2", "OVARIAN DYSGENESIS 2", "ovarian dysgenesis type 2", "premature ovarian failure 4", "Premature Ovarian Failure 4", "PREMATURE OVARIAN FAILURE 4", "BMP15 primary ovarian failure", "primary ovarian insufficiency 4", "ovarian dysgenesis, hypergonadotropic, X-linked", "OVARIAN DYSGENESIS, HYPERGONADOTROPIC, X-LINKED", "Ovarian Dysgenesis, Hypergonadotropic, X-Linked", "primary ovarian failure caused by mutation in BMP15", "ovarian failure, hypergonadotropic, due to ovarian dysgenesis", "Ovarian Failure, Hypergonadotropic, Due To Ovarian Dysgenesis", "OVARIAN FAILURE, HYPERGONADOTROPIC, DUE TO OVARIAN DYSGENESIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian dysgenesis 2", "shortest_name_length": 4}
{"curie": "UMLS:C1709881", "names": ["Refractory Cutaneous T-Cell Non-Hodgkin Lymphoma", "Refractory Cutaneous T-Cell Non-Hodgkin's Lymphoma", "Refractory Primary Cutaneous T-Cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Primary Cutaneous T-Cell Non-Hodgkin Lymphoma", "shortest_name_length": 48}
{"curie": "MONDO:0013005", "names": ["SESAMES", "EAST syndrome", "EAST SYNDROME", "SESAME SYNDROME", "sesame syndrome", "SeSAME syndrome", "SESAME syndrome", "Epilepsy, ataxia, sensorineural deafness and tubulopathy", "epilepsy, ataxia, sensorineural deafness and tubulopathy", "EPILEPSY, ATAXIA, SENSORINEURAL DEAFNESS, AND TUBULOPATHY", "Epilepsy, Ataxia, Sensorineural Deafness, And Tubulopathy", "epilepsy, ataxia, sensorineural deafness, and tubulopathy", "Epilepsy-ataxia-sensorineural deafness-tubulopathy syndrome", "Epilepsy-ataxia-sensorineural hearing loss-tubulopathy syndrome", "EAST (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome", "seizures, sensorineural deafness, ataxia, mental retardation and electrolyte imbalance", "Seizures, sensorineural deafness, ataxia, mental retardation and electrolyte imbalance", "Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, And Electrolyte Imbalance", "seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance", "seizures, sensorineural deafness, ataxia, intellectual disability and electrolyte imbalance", "seizures, sensorineural deafness, ataxia, intellectual disability, and electrolyte imbalance", "seizures - sensorineural deafness - ataxia - intellectual disability - electrolyte imbalance", "seizures-sensorineural deafness-ataxia-intellectual disability-electrolyte imbalance syndrome", "Seizures-sensorineural deafness-ataxia-intellectual disability-electrolyte imbalance syndrome", "Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome", "Seizures-sensorineural hearing loss-ataxia-intellectual disability-electrolyte imbalance syndrome", "SESAME (seizures, sensorineural deafness, ataxia, mental retardation, electrolyte imbalance) syndrome", "SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, IMPAIRED INTELLECTUAL DEVELOPMENT, AND ELECTROLYTE IMBALANCE", "Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome (disorder)", "Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "EAST syndrome", "shortest_name_length": 7}
{"curie": "UMLS:C4687701", "names": ["Pericardial Angiosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pericardial Angiosarcoma", "shortest_name_length": 24}
{"curie": "MONDO:0005355", "names": ["coronary restenosis", "Coronary Restenoses", "Coronary Restenosis", "Coronary restenosis", "Restenoses, Coronary", "Restenosis, Coronary", "Coronary artery restenosis", "coronary artery restenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coronary restenosis", "shortest_name_length": 19}
{"curie": "OMIM:132500", "names": ["hereditary epistaxis", "Hereditary epistaxis", "EPISTAXIS, HEREDITARY", "Epistaxis, Hereditary", "hereditary epistaxis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 20}
{"curie": "MONDO:0020084", "names": ["lymphoproliferative disease associated with primary immune disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphoproliferative disease associated with primary immune disease", "shortest_name_length": 66}
{"curie": "MONDO:0032617", "names": ["MC1DN11", "nuclear type mitochondrial complex I deficiency 11", "mitochondrial complex 1 deficiency, nuclear type 11", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 11", "shortest_name_length": 7}
{"curie": "UMLS:C1337016", "names": ["Well Differentiated Leiomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Well Differentiated Leiomyosarcoma", "shortest_name_length": 34}
{"curie": "UMLS:C0751845", "names": ["Middle Cerebral Artery Embolus", "Embolus, Middle Cerebral Artery"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Middle Cerebral Artery Embolus", "shortest_name_length": 30}
{"curie": "MONDO:0007360", "names": ["BOS2", "BO SYNDROME 2", "BO Syndrome 2", "bo syndrome 2", "BRANCHIOOTIC SYNDROME 2", "Branchiootic Syndrome 2", "branchiootic syndrome 2", "branchiootic syndrome type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "branchiootic syndrome 2", "shortest_name_length": 4}
{"curie": "MONDO:0043226", "names": ["Frommel Disease", "Frommel disease", "Disease, Frommel", "disease, Frommel", "frommel's disease", "Frommel's disease", "Frommel's Disease", "Disease, Frommel's", "disease, Frommel's", "Chiari Frommel syndrome", "Chiari Frommel Syndrome", "Chiari-Frommel syndrome", "Chiari-frommel syndrome", "chiari-frommel syndrome", "CHIARI-FROMMEL SYNDROME", "Chiari-Frommel Syndrome", "syndrome, Chiari-Frommel", "Syndrome, Chiari-Frommel", "Pregnancy-related A-G syndrome", "LACTATION WITH ATROPHY OF UTERUS", "postpartum amenorrhea-galactorrhea syndrome", "Postpartum amenorrhea-galactorrhea syndrome", "Postpartum amenorrhoea-galactorrhea syndrome", "postpartum amenorrhoea-galactorrhea syndrome", "Persistent postpartum amenorrhea-galactorrhea syndrome", "persistent postpartum amenorrhea-galactorrhea syndrome", "Postpartum amenorrhea-galactorrhea syndrome (disorder)", "Postpartum amenorrhea-galactorrhea syndrome (diagnosis)", "Persistent postpartum amenorrhoea-galactorrhoea syndrome", "puerperal complications amenorrhea-galactorrhea syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postpartum amenorrhea-galactorrhea syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0013554", "names": ["PSORS13", "psoriasis 13", "TRAF3IP2 psoriasis", "psoriasis susceptibility 13", "susceptibility to psoriasis 13", "PSORIASIS 13, SUSCEPTIBILITY TO", "psoriasis 13, susceptibility to", "psoriasis caused by mutation in TRAF3IP2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "psoriasis 13, susceptibility to", "shortest_name_length": 7}
{"curie": "MONDO:0024252", "names": ["global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome", "shortest_name_length": 105}
{"curie": "MONDO:0014916", "names": ["DEE41", "EIEE41", "early infantile epileptic encephalopathy 41", "developmental and epileptic encephalopathy 41", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 41", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 41", "epileptic encephalopathy, early infantile, 41", "developmental and epileptic encephalopathy, 41", "SLC1A2 early infantile epileptic encephalopathy", "epileptic encephalopathy, early infantile, type 41", "epileptic encephalopathy, early infantile, 41; EIEE41", "early infantile epileptic encephalopathy caused by mutation in SLC1A2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 41", "shortest_name_length": 5}
{"curie": "MONDO:0021046", "names": ["BFN", "breast fibroepithelial tumor", "Breast Fibroepithelial Tumor", "Breast Fibroepithelial Neoplasm", "breast fibroepithelial neoplasm", "breast fibroepithelial neoplasms"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast fibroepithelial neoplasm", "shortest_name_length": 3}
{"curie": "UMLS:C4520771", "names": ["Gastric Pylorus Carcinoma In Situ", "Stage 0 Gastric Pylorus Carcinoma", "Carcinoma in situ of Gastric Pylorus", "Carcinoma in situ of Pylorus of Stomach", "Carcinoma in situ of the Gastric Pylorus", "Carcinoma in situ of the Pylorus of the Stomach", "Gastric Pylorus Carcinoma In Situ AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Pylorus Carcinoma In Situ AJCC v6 and v7", "shortest_name_length": 33}
{"curie": "MONDO:0003212", "names": ["nasal cavity cancer", "Nasal cavity cancer", "Nasal Cavity Cancer", "nasal cavity carcinoma", "Nasal cavity carcinoma", "Nasal Cavity Carcinoma", "cancer of nasal cavity", "Cancer of Nasal Cavity", "Nasal cavity cancer NOS", "Carcinoma of nasal cavity", "carcinoma of nasal cavity", "Carcinoma of Nasal Cavity", "cancer of the nasal cavity", "Cancer of the Nasal Cavity", "carcinoma of the nasal cavity", "Carcinoma of the Nasal Cavity", "carcinoma of nasal cavity (diagnosis)", "Malignant epithelial neoplasm of nasal cavity", "Malignant epithelial neoplasm of nasal cavity (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasal cavity carcinoma", "shortest_name_length": 19}
{"curie": "MONDO:0004120", "names": ["Bartholin Gland Small Cell Carcinoma", "Bartholin gland small cell carcinoma", "Bartholin's Gland Small Cell Carcinoma", "Bartholin's gland small cell carcinoma", "major vestibular gland small cell carcinoma", "small cell carcinoma of major vestibular gland", "Bartholin Gland Small Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bartholin gland small cell carcinoma", "shortest_name_length": 36}
{"curie": "UMLS:C0334234", "names": ["Giant cell and spindle cell carcinoma", "giant cell and spindle cell carcinoma", "Giant Cell and Spindle Cell Carcinoma", "giant cell and spindle cell carcinoma (diagnosis)", "Giant cell and spindle cell carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Giant cell and spindle cell carcinoma", "shortest_name_length": 37}
{"curie": "UMLS:C1167945", "names": ["Infusion site rash"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infusion site rash", "shortest_name_length": 18}
{"curie": "MONDO:0002308", "names": ["GPC", "Giant Papillary Conjunctivitis", "giant papillary conjunctivitis", "Giant papillary conjunctivitis", "Papillary Conjunctivitis, Giant", "Conjunctivitis, Giant Papillary", "Giant Papillary Conjunctivitides", "Papillary Conjunctivitides, Giant", "Conjunctivitides, Giant Papillary", "GPC - Giant papillary conjunctivitis", "Giant papillary conjunctivitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "giant papillary conjunctivitis", "shortest_name_length": 3}
{"curie": "MONDO:0012087", "names": ["CILD4", "primary ciliary dyskinesia 4", "Primary ciliary dyskinesia, 4", "ciliary dyskinesia, primary, 4", "CILIARY DYSKINESIA, PRIMARY, 4", "Ciliary Dyskinesia, Primary, 4", "primary ciliary dyskinesia type 4", "primary ciliary dyskinesia 4 with or without situs inversus", "Ciliary Dyskinesia, Primary, 4, with or without Situs Inversus", "ciliary dyskinesia, primary, 4, with or without situs inversus", "CILIARY DYSKINESIA, PRIMARY, 4, WITH OR WITHOUT SITUS INVERSUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia 4", "shortest_name_length": 5}
{"curie": "MONDO:0033646", "names": ["MC4DN12", "mitochondrial complex 4 deficiency, nuclear type 12", "MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 12", "mitochondrial complex IV deficiency, nuclear type 12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 4 deficiency, nuclear type 12", "shortest_name_length": 7}
{"curie": "MONDO:0020843", "names": ["conjunctival diphtheria", "Conjunctival diphtheria", "Diphtheria, conjunctival", "Diphtheritic conjunctivitis", "CONJUNCTIVITIS, DIPHTHERITIC", "Conjunctival diphtheria (disorder)", "conjunctival diphtheria (diagnosis)", "Pseudomembranous diphtheritic conjunctivitis", "Pseudomembranous Diphtheritic Conjunctivitis", "pseudomembranous diphtheritic conjunctivitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudomembranous diphtheritic conjunctivitis", "shortest_name_length": 23}
{"curie": "MONDO:0008459", "names": ["Spinocerebellar Atrophy With Pupillary Paralysis", "SPINOCEREBELLAR ATROPHY WITH PUPILLARY PARALYSIS", "spinocerebellar atrophy with pupillary paralysis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar atrophy with pupillary paralysis", "shortest_name_length": 48}
{"curie": "UMLS:C0345604", "names": ["mixed parotid tumor", "Mixed parotid tumor", "Tumour;mixed parotid", "Mixed parotid tumour", "mixed parotid tumour", "Mixed Tumor of Parotid Gland", "Mixed parotid tumor (disorder)", "Mixed Tumor of the Parotid Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mixed parotid tumor", "shortest_name_length": 19}
{"curie": "MONDO:0022712", "names": ["oculo digital syndrome", "Chemke-Oliver-Mallek syndrome", "Chemke Oliver Mallek syndrome", "multiple ophthalmic anomalies and digital hypoplasia", "Multiple ophthalmic anomalies and digital hypoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculo digital syndrome", "shortest_name_length": 22}
{"curie": "UMLS:C5238244", "names": ["Refractory Triple-Negative Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Triple-Negative Breast Carcinoma", "shortest_name_length": 43}
{"curie": "UMLS:C0740387", "names": ["posterior cerebral artery aneurysm", "Posterior cerebral artery aneurysm", "Posterior Cerebral Artery Aneurysm", "Aneurysm, Posterior Cerebral Artery", "aneurysm of posterior cerebral artery", "Aneurysm of posterior cerebral artery", "Aneurysm of posterior cerebral artery (disorder)", "aneurysm of posterior cerebral artery (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aneurysm, Posterior Cerebral Artery", "shortest_name_length": 34}
{"curie": "MONDO:0005462", "names": ["PNET", "PNET, NOS", "neuroepithelioma", "Neuroepithelioma", "Neuroectodermal tumor", "Neuroectodermal Tumor", "neuroectodermal tumor", "Tumor, Neuroectodermal", "neuroectodermal tumors", "neuroectodermal; tumor", "Neuroectodermal Tumors", "Neuroectodermal tumour", "tumor; neuroectodermal", "Tumors, Neuroectodermal", "Neuroectodermal neoplasm", "Neuroectodermal Neoplasm", "neuroectodermal neoplasm", "Neuroectodermal tumor, NOS", "Neuroectodermal tumour, NOS", "primitive neuroectodermal tumor", "Primitive Neuroectodermal Tumor", "primitive Neuroectodermal neoplasm", "primitive neuroectodermal neoplasm", "Primitive Neuroectodermal Neoplasm", "Primitive neuroectodermal tumor, NOS", "primitive neuroectodermal tumor (PNET)", "Primitive Neuroectodermal Tumor (PNET)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primitive neuroectodermal tumor", "shortest_name_length": 4}
{"curie": "UMLS:C4743986", "names": ["Bilateral Proliferative Retinopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bilateral Proliferative Retinopathy", "shortest_name_length": 35}
{"curie": "MONDO:0001288", "names": ["Vaginal Endometriosis", "vaginal endometriosis", "Endometriosis of rectovaginal septum and vagina", "endometriosis of rectovaginal septum and vagina", "endometriosis of rectovaginal septum and vagina (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometriosis of rectovaginal septum and vagina", "shortest_name_length": 21}
{"curie": "MONDO:0045053", "names": ["osseous tumor", "Osseous Tumor", "osseous neoplasm", "Osseous Neoplasm", "Osteogenic Tumor", "osteogenic tumor", "Osteogenic Neoplasm", "osteogenic neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteogenic neoplasm", "shortest_name_length": 13}
{"curie": "UMLS:C4331917", "names": ["Nasopharyngeal Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasopharyngeal Carcinoma by AJCC v8 Stage", "shortest_name_length": 41}
{"curie": "MONDO:0012807", "names": ["EBSPA", "EBS5C", "Ebs-Pa", "EBS-PA", "Ebs With Pyloric Atresia", "EBS with pyloric atresia", "epidermolysis bullosa simplex with pyloric atresia", "Epidermolysis Bullosa Simplex With Pyloric Atresia", "Epidermolysis bullosa simplex with pyloric atresia", "EPIDERMOLYSIS BULLOSA SIMPLEX WITH PYLORIC ATRESIA", "EPIDERMOLYSIS BULLOSA SIMPLEX 5C, WITH PYLORIC ATRESIA", "epidermolysis bullosa simplex 5C, with pyloric atresia", "Epidermolysis bullosa simplex co-occurrent with pyloric atresia", "Epidermolysis bullosa simplex co-occurrent with pyloric atresia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolysis bullosa simplex 5C, with pyloric atresia", "shortest_name_length": 5}
{"curie": "MONDO:0009198", "names": ["lethal congenital erythroderma", "Congenital lethal erythroderma", "Lethal congenital erythroderma", "Erythroderma lethal congenital", "erythroderma lethal congenital", "congenital lethal erythroderma", "Erythroderma, Lethal Congenital", "ERYTHRODERMA, LETHAL CONGENITAL", "erythroderma, lethal congenital", "Congenital lethal erythroderma (disorder)", "congenital exfoliative erythroderma resistant to treatment"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital lethal erythroderma", "shortest_name_length": 30}
{"curie": "MONDO:0021111", "names": ["ureter tumor", "Ureter Tumor", "tumor ureter", "tumors ureter", "Ureteral Tumor", "ureteral tumor", "ureter neoplasm", "tumor of ureter", "Ureter Neoplasm", "Tumor of ureter", "Tumor of Ureter", "Ureters--Tumors", "Tumour of ureter", "Ureter Neoplasms", "ureteral neoplasm", "ureter, cancer of", "Ureteral Neoplasm", "Ureteral neoplasm", "neoplasm of ureter", "ureteral neoplasms", "Neoplasm of ureter", "Neoplasm of Ureter", "Neoplasm, Ureteral", "Ureteral Neoplasms", "neoplasms of ureter", "Tumor of the Ureter", "Neoplasms, Ureteral", "Neoplasms of Ureter", "tumor of the ureter", "Ureteral neoplasm NOS", "neoplasm of the ureter", "Neoplasm of the Ureter", "Neoplasm of the ureter", "Neoplasms of the Ureter", "neoplasms of the ureter", "Neoplasia of the ureters", "ureter neoplasm (disease)", "Neoplasm of ureter (disorder)", "neoplasm of ureter (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ureter neoplasm", "shortest_name_length": 12}
{"curie": "MONDO:0006577", "names": ["Maxillary Sinus Cholesteatoma", "maxillary sinus cholesteatoma", "maxillary sinus cholesteatoma (disease)", "cholesteatoma (disease) of maxillary sinus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maxillary sinus cholesteatoma", "shortest_name_length": 29}
{"curie": "MONDO:0007973", "names": ["mental and growth retardation with amblyopia", "Mental and Growth Retardation with Amblyopia", "MENTAL AND GROWTH RETARDATION WITH AMBLYOPIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mental and growth retardation with amblyopia", "shortest_name_length": 44}
{"curie": "UMLS:C1848186", "names": ["Malignant sex-cord stromal tumor", "Malignant Sex Cord-Stromal Tumor", "STROMAL TUMOR, GONADAL, MALIGNANT", "Sex Cord Stromal Tumor, Malignant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant sex-cord stromal tumor", "shortest_name_length": 32}
{"curie": "MONDO:0019079", "names": ["SMA", "proximal spinal muscular atrophy", "Proximal spinal muscular atrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "proximal spinal muscular atrophy", "shortest_name_length": 3}
{"curie": "UMLS:C3640025", "names": ["Acquired Bilateral Cataracts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired Bilateral Cataracts", "shortest_name_length": 28}
{"curie": "UMLS:C4527069", "names": ["stage IIA Merkel cell carcinoma", "Pathologic Stage IIA Merkel Cell Carcinoma AJCC v8", "pathologic stage IIA Merkel cell carcinoma AJCC v8", "pathologic stage IIA neuroendocrine carcinoma of the skin AJCC v8", "Pathologic Stage IIA Neuroendocrine Carcinoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IIA Merkel Cell Carcinoma AJCC v8", "shortest_name_length": 31}
{"curie": "UMLS:C1698195", "names": ["Small intestinal anastomotic leak", "Small Intestinal Anastomotic Leakage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Intestinal Anastomotic Leakage", "shortest_name_length": 33}
{"curie": "UMLS:C2828203", "names": ["Stage IIB Bone Cancer", "Stage IIB Bone Cancer AJCC v7", "Stage IIB Bone Cancer  AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Bone Cancer AJCC v7", "shortest_name_length": 21}
{"curie": "MONDO:0003783", "names": ["lymphopenia", "Lymphopenia", "LYMPHOPENIA", "Lymphopenias", "alymphocytosis", "Alymphocytosis", "lymphocytopenia", "Lymphocytopenia", "LYMPHOCYTOPENIA", "Lymphocytopenias", "decreased lymphocyte", "Lymphocytopenia, NOS", "decreased lymphocytes", "Low lymphocyte number", "Decreased lymphocytes", "lymphopenia (disease)", "lymphopenia (diagnosis)", "Lymphocytopenia (disorder)", "lymphocytopenia (diagnosis)", "Decreased blood lymphocyte number", "Absolute lymphocyte count decrease", "Disorder characterized by lymphopenia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphopenia", "shortest_name_length": 11}
{"curie": "MONDO:0017347", "names": ["PBL", "PLBL", "plasmablastic lymphoma", "Plasmablastic lymphoma", "Plasmablastic Lymphoma", "Plasmablastic Lymphomas", "Lymphoma, Plasmablastic", "Lymphomas, Plasmablastic", "Plasmablastic lymphoma (disorder)", "plasmablastic lymphoma (diagnosis)", "Plasmablasts Diffuse Large B-cell Lymphoma", "Plasmablasts Diffuse Large B cell Lymphoma", "Plasmablastic Diffuse Large B-cell Lymphoma", "Plasmablastic diffuse large B-cell lymphoma", "Plasmablastic Diffuse Large B cell Lymphoma", "Plasmablastic lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "plasmablastic lymphoma", "shortest_name_length": 3}
{"curie": "UMLS:C1336827", "names": ["Tropical Disease", "Tropical Diseases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tropical Disease", "shortest_name_length": 16}
{"curie": "MONDO:0000167", "names": ["Huntington disease and related disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Huntington disease and related disorders", "shortest_name_length": 40}
{"curie": "UMLS:C0751584", "names": ["West Nile Fever Meningitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "West Nile Fever Meningitis", "shortest_name_length": 26}
{"curie": "MONDO:0014894", "names": ["MGORS7", "MEIER-GORLIN SYNDROME 7", "Meier-Gorlin syndrome 7", "CDC45 Meier-Gorlin syndrome", "Meier-Gorlin syndrome type 7", "Meier-Gorlin syndrome 7; MGORS7", "Meier-Gorlin syndrome caused by mutation in CDC45"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meier-Gorlin syndrome 7", "shortest_name_length": 6}
{"curie": "MONDO:0019720", "names": ["isolated renal or urinary tract malformation", "nonsyndromic renal or urinary tract malformation", "non-syndromic renal or urinary tract malformation", "isolated congenital anomaly of kidney and urinary tract", "nonsyndromic congenital anomaly of kidney and urinary tract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-syndromic renal or urinary tract malformation", "shortest_name_length": 44}
{"curie": "MONDO:0009830", "names": ["PKPS", "PARK15", "Parkinson's disease 15", "Pallido-pyramidal disease", "Pallidopyramidal syndrome", "PALLIDOPYRAMIDAL SYNDROME", "pallido-pyramidal disease", "pallidopyramidal syndrome", "pallido-pyramidal syndrome", "Pallido-Pyramidal Syndrome", "PALLIDO-PYRAMIDAL SYNDROME", "Parkinsonian pyramidal syndrome", "Parkinsonian-pyramidal syndrome", "PARKINSONIAN-PYRAMIDAL SYNDROME", "parkinsonian-pyramidal syndrome", "Parkinsonian-Pyramidal Syndrome", "Parkinson disease 15, autosomal recessive", "Parkinson Disease 15, Autosomal Recessive", "PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE", "Parkinsonian pyramidal syndrome (disorder)", "PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE (disorder)", "autosomal recessive early-onset Parkinson disease 15", "PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET", "Parkinson disease 15, autosomal recessive early-onset", "autosomal recessive early-onset Parkinson's disease 15", "autosomal recessive early-onset Parkinson disease type 15"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parkinsonian-pyramidal syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0010886", "names": ["BDMR", "Del(2)(q37)", "Deletion 2q37", "deletion 2q37", "2q37 monosomy", "Monosomy 2q37", "Monosomy 2q37qter", "monosomy 2q37qter", "monosomy 2q37-qter", "deletion 2q37-qter", "2q37 deletion syndrome", "2q37 microdeletion syndrome", "Chromosome 2, monosomy 2q37", "Chromosome 2q37 deletion syndrome", "CHROMOSOME 2q37 DELETION SYNDROME", "chromosome 2q37 deletion syndrome", "Chromosome 2q37 Deletion Syndrome", "brachydactyly-mental retardation syndrome", "Brachydactyly mental retardation syndrome", "Albright hereditary osteodystrophy type 3", "Brachydactyly Mental Retardation Syndrome", "Brachydactyly-Mental Retardation syndrome", "brachydactyly mental retardation syndrome", "BRACHYDACTYLY-MENTAL RETARDATION SYNDROME", "Chromosome 2q37 deletion syndrome (disorder)", "brachydactyly intellectual disability syndrome", "Brachydactyly-intellectual disability syndrome", "brachydactyly-intellectual disability syndrome", "ALBRIGHT HEREDITARY OSTEODYSTROPHY-LIKE SYNDROME", "Albright hereditary osteodystrophy-like syndrome", "Albright's hereditary osteodystrophy-like syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "2q37 microdeletion syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0005048", "names": ["insulinoma", "Beta cell tumor", "Beta Cell Tumor", "beta cell neoplasm", "pancreatic Beta cell tumor", "Pancreatic Beta Cell Tumor", "Beta Cell Tumor of Pancreas", "Beta cell tumor of pancreas", "Beta Cell Tumor of the Pancreas", "Beta cell tumor of the pancreas", "beta cell tumor of the pancreas", "Pancreatic Insulin Producing NET", "pancreatic insulin producing NET", "insulin-producing islet cell tumor", "Pancreatic Insulin Producing Tumor", "pancreatic insulin producing tumor", "pancreatic insulin-producing tumor", "Insulin-Producing Islet Cell Tumor", "Pancreatic Insulin Producing Neoplasm", "pancreatic insulin producing neoplasm", "insulin-producing tumor of islet cells", "Insulin-Producing Tumor of Islet Cells", "Insulin-Producing Tumor of the Islet Cells", "insulin-producing tumor of the islet cells", "Pancreatic Insulin-Producing Neuroendocrine Tumor", "pancreatic insulin-producing neuroendocrine tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic insulin-producing neuroendocrine tumor", "shortest_name_length": 10}
{"curie": "MONDO:0007680", "names": ["MNG/CRD/Da", "MNG/CRD/DA", "Daneman Davy Mancer syndrome", "Daneman-Davy-Mancer syndrome", "Thyroid-renal-digital anomalies", "thyroid-renal-digital anomalies", "Thyroid, renal, digital anomaly syndrome", "multinodular goiter - cystic kidney - polydactyly", "multinodular goiter-cystic kidney-polydactyly syndrome", "Multinodular goiter-cystic kidney-polydactyly syndrome", "Multinodular goitre, cystic kidney, polydactyly syndrome", "Multinodular goiter, cystic kidney, polydactyly syndrome", "MULTINODULAR GOITER/CYSTIC RENAL DISEASE/DIGITAL ANOMALIES", "Multinodular Goiter-Cystic Renal Disease-Digital Anomalies", "multinodular goiter/cystic renal disease/digital anomalies", "multinodular goiter, cystic renal disease, and digital anomalies", "Multinodular goiter, cystic renal disease, and digital anomalies", "Goiter, Multinodular, Cystic Renal Disease, and Digital Anomalies", "GOITER, MULTINODULAR, CYSTIC RENAL DISEASE, AND DIGITAL ANOMALIES", "goiter, multinodular, cystic renal disease, and digital anomalies", "Multinodular goiter, cystic kidney, polydactyly syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multinodular goiter-cystic kidney-polydactyly syndrome", "shortest_name_length": 10}
{"curie": "MONDO:0024757", "names": ["Cardiovascular Tumor", "cardiovascular tumor", "cardiovascular neoplasm", "Cardiovascular Neoplasm", "cardiovascular system tumor", "tumor of cardiovascular system", "cardiovascular system neoplasm", "neoplasm of cardiovascular system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiovascular neoplasm", "shortest_name_length": 20}
{"curie": "UMLS:C0856027", "names": ["Stage IV Splenic Marginal Zone Lymphoma", "Splenic Marginal Zone Lymphoma Stage IV", "Splenic marginal zone lymphoma stage IV", "Stage IV Splenic Marginal Zone B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Splenic marginal zone lymphoma stage IV", "shortest_name_length": 39}
{"curie": "MONDO:0009091", "names": ["CPHD3", "Winkelman Bethge Pfeiffer syndrome", "Winkelmann-Bethge-Pfeiffer syndrome", "PITUITARY HORMONE DEFICIENCY, COMBINED, 3", "pituitary hormone deficiency, combined, 3", "Pituitary Hormone Deficiency, Combined, 3", "pituitary hormone deficiency, combined, type 3", "Sensorineural deafness with Pituitary dwarfism", "Deafness, sensorineural with pituitary dwarfism", "Deafness, Sensorineural, With Pituitary Dwarfism", "DEAFNESS, SENSORINEURAL, WITH PITUITARY DWARFISM", "deafness, sensorineural, with pituitary dwarfism", "Pituitary hormone deficiency, combined with rigid cervical spine", "pituitary hormone deficiency, combined, with rigid cervical spine", "PITUITARY HORMONE DEFICIENCY, COMBINED, WITH RIGID CERVICAL SPINE", "Pituitary Hormone Deficiency, Combined, With Rigid Cervical Spine", "non-acquired combined pituitary hormone deficiency with spine abnormalities", "non-acquired combined pituitary hormone deficiency-deafness-rigid cervical spine syndrome", "non-acquired combined pituitary hormone deficiency-sensorineural hearing loss-spine abnormalities syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-acquired combined pituitary hormone deficiency with spine abnormalities", "shortest_name_length": 5}
{"curie": "MONDO:0006579", "names": ["Melanoacanthoma", "melanoacanthoma", "Melanoacanthoma (disorder)", "pigmented seborrheic keratosis", "Pigmented seborrheic keratosis", "Pigmented seborrhoeic keratosis", "pigmented seborrheic keratosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melanoacanthoma", "shortest_name_length": 15}
{"curie": "UMLS:C5669823", "names": ["Refractory Pancreatobiliary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Pancreatobiliary Carcinoma", "shortest_name_length": 37}
{"curie": "UMLS:C1456865", "names": ["Stone;ureter", "ureteric stone", "Ureteral stone", "Ureteric Stone", "URETERAL STONE", "URETER CALCULUS", "Calculus;ureter", "calculus; ureter", "ureter; calculus", "Ureteral calculi", "Ureteral Calculi", "URETER, CALCULUS", "URETERAL CALCULUS", "Calculi, Ureteral", "Ureteric Calculus", "Calculus ureteral", "Calculus ureteric", "Ureteral Calculus", "Ureteral calculus", "ureteric calculus", "Ureteric calculus", "CALCULUS URETERAL", "Calculus of ureter", "Calculus, Ureteral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ureteral Calculi", "shortest_name_length": 12}
{"curie": "UMLS:C0281940", "names": ["Pelvic peritonitis", "peritonitis pelvic", "Pelvic Peritonitis", "pelvic peritonitis", "Pelvic peritonitis (disorder)", "pelvic peritonitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pelvic peritonitis", "shortest_name_length": 18}
{"curie": "UMLS:C0015459", "names": ["Face Injury", "FACE INJURY", "wound; face", "face injury", "face; wound", "Face injury", "facial injury", "Facial Injury", "injury facial", "face injuries", "wound of face", "Facial injury", "Injury, Facial", "injury of face", "Injury of face", "facial injuries", "Facial Injuries", "injuries facial", "Injuries, Facial", "Injury of face NOS", "Injury of face (disorder)", "injury of face (diagnosis)", "wound of face (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Facial Injuries", "shortest_name_length": 11}
{"curie": "MONDO:0006512", "names": ["ER+ breast cancer", "estrogen receptor positive breast cancer", "estrogen-receptor positive breast cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "estrogen-receptor positive breast cancer", "shortest_name_length": 17}
{"curie": "UMLS:C4329629", "names": ["CNS Embryonal tumor with rhabdoid features", "CNS Embryonal Tumor with Rhabdoid Features", "Central Nervous System Embryonal Tumor with Rhabdoid Features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Embryonal Tumor with Rhabdoid Features", "shortest_name_length": 42}
{"curie": "MONDO:0011276", "names": ["OFC2", "OROFACIAL CLEFT 2", "orofacial cleft 2", "Orofacial Cleft 2", "nonsyndromic cleft lip with or without cleft palate 2", "cleft lip with or without cleft palate, nonsyndromic, 2", "CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 2", "Cleft Lip with or without Cleft Palate, Nonsyndromic, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orofacial cleft 2", "shortest_name_length": 4}
{"curie": "UMLS:C0334448", "names": ["Giant blue nevus", "Cellular Blue Nevi", "Blue Nevi, Cellular", "Nevi, Cellular Blue", "Cellular blue nevus", "cellular blue nevus", "Cellular Blue Nevus", "Blue Nevus, Cellular", "Nevus, Cellular Blue", "Cellular blue naevus", "Cellular Blue Nevus of Skin", "Cellular blue nevus of skin", "Cellular blue naevus of skin", "Cellular Blue Nevus of the Skin", "Cellular blue nevus of skin (disorder)", "Cellular blue nevus (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cellular Blue Nevus", "shortest_name_length": 16}
{"curie": "MONDO:0011904", "names": ["BFIC3", "BFIS3", "BFNIS", "benign neonatal-infantile epilepsy", "epilepsy, benign neonatal-infantile", "convulsions benign familial neonatal", "benign familial infantile seizures 3", "Benign Familial Infantile Seizures, 3", "benign familial infantile convulsions", "Seizures, Benign Familial Infantile, 3", "seizures, benign familial infantile, 3", "SEIZURES, BENIGN FAMILIAL INFANTILE, 3", "SCN2A benign familial infantile epilepsy", "convulsions, benign familial infantile, 3", "CONVULSIONS, BENIGN FAMILIAL INFANTILE, 3", "Convulsions, Benign Familial Infantile, 3", "benign familial neonatal-infantile seizures", "seizures, benign familial infantile, type 3", "SEIZURES, BENIGN FAMILIAL NEONATAL-INFANTILE", "seizures, benign familial neonatal-infantile", "benign familial infantile epilepsy caused by mutation in SCN2A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "seizures, benign familial infantile, 3", "shortest_name_length": 5}
{"curie": "MONDO:0030430", "names": ["SPGF56", "SPERMATOGENIC FAILURE 56", "spermatogenic failure 56"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 56", "shortest_name_length": 6}
{"curie": "MONDO:0005129", "names": ["cataract", "CATARACT", "Cataract", "Cataracts", "CATARACTS", "cataracts", "Cloudy lens", "CATARACT NOS", "Lens Opacity", "Lens opacity", "Cataract NOS", "LENS OPACITY", "lens opacity", "opacity; lens", "Opacity, lens", "Cataract form", "Cataract, NOS", "Opacity, Lens", "lens; opacity", "Other cataract", "Lens Opacities", "Lens opacities", "Opacities, Lens", "LO - Lens opacity", "lenticular opacity", "Lenticular opacity", "LENTICULAR OPACITY", "OPACITY LENTICULAR", "Opacity lenticular", "cataract (disease)", "Cataract (disorder)", "opacity of the lens", "Cataract unspecified", "CATARACT UNSPECIFIED", "Unspecified cataract", "lenticular opacities", "Lenticular opacities", "cataract (diagnosis)", "Cataract, unspecified", "eye disease; cataract", "cataract; eye disease", "Lens opacity (finding)", "Clouding of the lens of the eye", "Cataract form (observable entity)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract", "shortest_name_length": 8}
{"curie": "MONDO:0005382", "names": ["Paget; bone", "bone; Paget", "Paget disease", "PAGET DISEASE", "Paget's Disease", "paget's disease", "Paget's disease", "PAGET DISEASE BONE", "paget bone disease", "OSTEITIS DEFORMANS", "bone Paget disease", "Bone Paget Disease", "Osteitis deformans", "Osteitis Deformans", "osteitis deformans", "PAGET DISEASE, BONE", "Paget Disease, Bone", "osteitis; deformans", "deformans; osteitis", "bone Paget's disease", "Bone Paget's Disease", "PAGET'S BONE DISEASE", "Pagets Disease, Bone", "Paget's bone disease", "paget's bone disease", "Pagets disease (bone)", "Paget Disease of Bone", "Paget disease of bone", "Pagets Disease (Bone)", "Disease;Pagets (bone)", "Pagets (bone) disease", "PAGETS DISEASE OF BONE", "Pagets disease of bone", "Paget's disease (bone)", "osseous Paget's disease", "paget's disease of bone", "Osseous Paget's Disease", "Paget's disease of bone", "PAGET'S DISEASE OF BONE", "Paget's Disease of Bone", "osteitis deformans; Paget", "Paget; osteitis deformans", "Paget's disease (diagnosis)", "Paget's Disease of the Bone", "paget's disease of the bone", "PAGET'S DISEASE OF THE BONE", "Paget's disease of the bone", "Osteitis deformans (disorder)", "Familial Paget's disease of bone", "familial Paget's disease of bone", "Unspecified Paget's disease of bone", "Paget's disease of bone, unspecified", "Osteitis deformans [Paget's disease of bone]", "Paget's disease of bone [osteitis deformans]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bone Paget disease", "shortest_name_length": 11}
{"curie": "MONDO:0021114", "names": ["Bartholin's Gland Tumor", "Bartholin's gland tumor", "Bartholin Gland Neoplasm", "Bartholin gland neoplasm", "Bartholin's gland neoplasm", "Tumor of Bartholin's Gland", "Bartholin's Gland Neoplasm", "tumor of Bartholin's gland", "major vestibular gland tumor", "Neoplasm of Bartholin's Gland", "neoplasm of Bartholin's gland", "Tumor of the Bartholin's Gland", "tumor of the Bartholin's gland", "tumor of major vestibular gland", "major vestibular gland neoplasm", "Neoplasm of the Bartholin's Gland", "neoplasm of the Bartholin's gland", "neoplasm of major vestibular gland", "major vestibular gland neoplasm (disease)", "neoplasm of Bartholin's gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bartholin gland neoplasm", "shortest_name_length": 23}
{"curie": "MONDO:0007454", "names": ["T1D2", "IDDM2", "type 1 diabetes mellitus 2", "TYPE 1 DIABETES MELLITUS 2", "INS type 1 diabetes mellitus", "insulin-dependent diabetes mellitus 2", "Insulin-Dependent Diabetes Mellitus 2", "INSULIN-DEPENDENT DIABETES MELLITUS 2", "Diabetes Mellitus, Insulin-Dependent, 2", "diabetes mellitus, insulin-dependent, 2", "DIABETES MELLITUS, INSULIN-DEPENDENT, 2", "diabetes mellitus, insulin-dependent, type 2", "type 1 diabetes mellitus caused by mutation in INS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type 1 diabetes mellitus 2", "shortest_name_length": 4}
{"curie": "UMLS:C0153256", "names": ["Meningitis candida", "candidal meningitis", "Candidal meningitis", "Candidal meningitis (disorder)", "candidal meningitis (diagnosis)", "meningitis; candidiasis (manifestation)", "candidiasis; meningitis (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Candidal meningitis", "shortest_name_length": 18}
{"curie": "MONDO:0003561", "names": ["malignant Osteoclastoma", "Giant Cell Fibrous Histiocytoma", "giant cell fibrous histiocytoma", "Malignant Giant Cell Tumor of Soft Parts", "malignant giant cell tumor of soft parts", "Malignant giant cell tumor of soft parts", "Malignant giant cell tumor of soft tissue", "giant cell malignant fibrous histiocytoma", "Malignant giant cell tumour of soft parts", "Giant Cell Malignant Fibrous Histiocytoma", "Malignant giant cell fibrous histiocytoma", "Malignant giant cell tumour of soft tissue", "malignant Giant cell neoplasm of soft Parts", "Malignant Giant Cell Neoplasm of Soft Parts", "malignant giant cell neoplasm of soft parts", "malignant giant cell tumor of soft parts (morphologic abnormality)", "Malignant giant cell tumor of soft parts (morphologic abnormality)", "undifferentiated pleomorphic sarcoma with osteoclast-like giant cells", "Undifferentiated Pleomorphic Sarcoma with Osteoclast-Like Giant Cells"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant giant cell tumor of soft parts", "shortest_name_length": 23}
{"curie": "MONDO:0022205", "names": ["Pustular psoriasis", "psoriasis pustular", "pustular psoriasis", "Psoriasis pustular", "PSORIASIS PUSTULAR", "psoriasis; pustular", "pustular; psoriasis", "PSORIASIS, PUSTULAR", "PSEUDOPSORIASIS, PUSTULAR", "Pustular psoriasis (disorder)", "pustular psoriasis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pustular psoriasis", "shortest_name_length": 18}
{"curie": "MONDO:0034216", "names": ["resistance to thyroid hormone alpha", "resistance to thyroid hormone due to a mutation in thyroid hormone receptor alpha"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "resistance to thyroid hormone due to a mutation in thyroid hormone receptor alpha", "shortest_name_length": 35}
{"curie": "MONDO:0002402", "names": ["giant cell type neoplasm", "Malignant giant cell tumor", "Malignant Giant Cell Tumor", "malignant giant cell tumor", "Malignant giant cell tumour", "GIANT CELL TUMOR, MALIGNANT", "giant cell tumor, malignant", "Malignant Giant Cell Neoplasm", "malignant Giant cell neoplasm", "malignant giant cell neoplasm", "malignant tumor, giant cell type", "Malignant tumor, giant cell type", "Malignant tumor - giant cell type", "Malignant tumour, giant cell type", "Malignant tumour - giant cell type", "tumor; malignant, giant cell (type)", "tumor; giant cell (type), malignant", "giant cell type neoplasm (diagnosis)", "malignant tumor, giant cell type (morphologic abnormality)", "Malignant tumor, giant cell type (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant giant cell tumor", "shortest_name_length": 24}
{"curie": "MONDO:0000244", "names": ["endothrix infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endothrix infectious disease", "shortest_name_length": 28}
{"curie": "MONDO:0010650", "names": ["MNS", "Osteodysplasty", "osteodysplasty", "melnick needle syndrome", "melnick needles syndrome", "Melnick-Needles Syndrome", "MELNICK-NEEDLES SYNDROME", "MELNICK-NEEDLES syndrome", "Melnick Needles Syndrome", "melnick-needles syndrome", "Melnick-Needles syndrome", "Melnick Needles Osteodysplasty", "MELNICK-NEEDLES OSTEODYSPLASTY", "Melnick-Needles osteodysplasty", "Melnick-Needles Osteodysplasty", "Osteodysplasty, Melnick-Needles", "Melnick-Needles syndrome (disorder)", "Osteodysplasty of Melnick and Needles", "OSTEODYSPLASTY OF MELNICK AND NEEDLES", "osteodysplasty of Melnick and Needles", "Melnick-Needles syndrome, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Melnick-Needles syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C1328291", "names": ["Dysesthesia pharynx", "Dysaesthesia pharynx"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dysesthesia pharynx", "shortest_name_length": 19}
{"curie": "UMLS:C0339807", "names": ["House dust allergy", "Allergy to house dust", "Allergy to house dust (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "House dust allergy", "shortest_name_length": 18}
{"curie": "MONDO:0015647", "names": ["Thinking seizures", "Thinking epilepsy", "thinking seizures", "epilepsy reflex thinking", "Thinking epilepsy (disorder)", "Thinking epilepsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thinking seizures", "shortest_name_length": 17}
{"curie": "MONDO:0016814", "names": ["MILS", "mtDNA-associated Leigh syndrome", "Maternally inherited Leigh disease", "Maternally-inherited Leigh disease", "maternally-inherited Leigh disease", "maternally-inherited Leigh syndrome", "Maternally inherited Leigh syndrome", "Maternally Inherited Leigh Syndrome", "Leigh disease, maternally inherited", "maternally inherited Leigh syndrome", "mitochondrial DNA-associated Leigh syndrome", "Mitochondrial DNA-associated Leigh syndrome", "Maternally inherited Leigh syndrome (disorder)", "Subacute necrotizing encephalomyelopathy maternally inherited", "Maternally inherited infantile subacute necrotizing encephalopathy", "maternally-inherited infantile subacute necrotizing encephalopathy", "Maternally-inherited infantile subacute necrotizing encephalopathy", "Maternally inherited infantile subacute necrotising encephalopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maternally-inherited Leigh syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0017239", "names": ["FPHH", "familial progressive hyper- and hypopigmentation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial progressive hyper- and hypopigmentation", "shortest_name_length": 4}
{"curie": "MONDO:0004650", "names": ["carotid body cancer", "cancer of carotid body", "Cancer of carotid body", "chemodectoma, malignant", "CHEMODECTOMA, MALIGNANT", "Malignant Carotid Body Tumor", "Malignant carotid body tumor", "carotid body tumor malignant", "malignant carotid body tumor", "Malignant carotid body tumour", "Malignant Carotid Body Neoplasm", "Malignant Tumor of Carotid Body", "malignant carotid body neoplasm", "malignant tumor of carotid body", "Malignant Neoplasm of Carotid Body", "Malignant neoplasm of carotid body", "malignant neoplasm of carotid body", "malignant tumor of the carotid body", "Malignant Tumor of the Carotid Body", "Malignant Carotid Body Paraganglioma", "malignant Carotid body Paraganglioma", "malignant carotid body paraganglioma", "Metastatic Carotid Body Paraganglioma", "carotid body paraganglioma, malignant", "Malignant Neoplasm of the Carotid Body", "malignant neoplasm of the carotid body", "Malignant neoplasm of carotid body (disorder)", "malignant neoplasm of carotid body (diagnosis)", "Malignant carotid body tumor (morphologic abnormality)", "malignant carotid body tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant carotid body paraganglioma", "shortest_name_length": 19}
{"curie": "UMLS:C0267019", "names": ["Oral pyogenic granuloma", "Oral Mucosa Pyogenic Granuloma", "pyogenic; granuloma, oral mucosa", "Pyogenic Granuloma of Oral Mucosa", "pyogenic granuloma of oral mucosa", "Pyogenic granuloma of oral mucosa", "Pyogenic Granuloma of the Oral Mucosa", "Oral Mucosa Lobular Capillary Hemangioma", "Pyogenic granuloma of oral mucosa (disorder)", "pyogenic granuloma of oral mucosa (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pyogenic granuloma of oral mucosa", "shortest_name_length": 23}
{"curie": "UMLS:C1335487", "names": ["Primary Intraosseous Carcinoma Ex Odontogenic Cyst", "Primary Intraosseous Squamous Cell Carcinoma Derived From Odontogenic Cyst"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Intraosseous Squamous Cell Carcinoma Derived From Odontogenic Cyst", "shortest_name_length": 50}
{"curie": "UMLS:C3495846", "names": ["KS-IRIS", "IRIS-KS", "IRIS-Associated KS", "KS-Associated IRIS", "IRIS associated Kaposi's sarcoma", "Kaposi Sarcoma Immune Reconstitution Syndrome", "Kaposi Sarcoma-Associated Immune Reconstitution Syndrome", "Immune reconstitution inflammatory syndrome associated Kaposi's sarcoma", "Immune Reconstitution Inflammatory Syndrome Associated with Kaposi Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immune reconstitution inflammatory syndrome associated Kaposi's sarcoma", "shortest_name_length": 7}
{"curie": "UMLS:C5419191", "names": ["Advanced Unclassified Renal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Unclassified Renal Cell Carcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0016216", "names": ["adult HCC", "Adult HCC", "Adult Hepatoma", "adult hepatoma", "hepatocellular cancer", "Hepatocellular Cancer", "adult primary hepatoma", "Adult Primary Hepatoma", "hepatoma, adult primary", "adult hepatocellular carcinoma", "Adult hepatocellular carcinoma", "Adult Hepatocellular Carcinoma", "Adult Primary Liver Cell Carcinoma", "adult primary liver cell carcinoma", "hepatocellular carcinoma of adults", "Adult HCC (hepatocellular carcinoma)", "Adult Primary Carcinoma of Liver Cell", "adult primary carcinoma of liver cell", "Adult Primary Hepatocellular Carcinoma", "adult primary hepatocellular carcinoma", "hepatocellular carcinoma, adult primary", "Adult Primary Carcinoma of the Liver Cell", "adult primary carcinoma of the liver cell", "Adult hepatocellular carcinoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult hepatocellular carcinoma", "shortest_name_length": 9}
{"curie": "MONDO:0008780", "names": ["ALSJ", "ALS2", "ALS, juvenile", "ALS, Juvenile", "ALS, JUVENILE", "ALS2 (diagnosis)", "amyotrophic lateral sclerosis 2", "amyotrophic lateral sclerosis ALS2", "ALS2 amyotrophic lateral sclerosis", "amyotrophic lateral sclerosis type 2", "amyotrophic lateral sclerosis 2, juvenile", "Amyotrophic Lateral Sclerosis 2, Juvenile", "AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE", "amyotrophic lateral sclerosis type 2, juvenile", "AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE (disorder)", "amyotrophic lateral sclerosis caused by mutation in ALS2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyotrophic lateral sclerosis type 2, juvenile", "shortest_name_length": 4}
{"curie": "MONDO:0017846", "names": ["AD-SPAX", "autosomal dominant spastic ataxia", "spastic ataxia, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant spastic ataxia", "shortest_name_length": 7}
{"curie": "UMLS:C0686457", "names": ["malignant conjunctival neoplasm secondary", "secondary malignant conjunctival neoplasm", "Secondary malignant neoplasm of conjunctiva", "secondary malignant neoplasm of conjunctiva", "Metastatic malignant neoplasm to conjunctiva", "Metastatic malignant neoplasm of conjunctiva", "Metastatic Malignant Neoplasm in the Conjunctiva", "secondary malignant neoplasm of conjunctiva (diagnosis)", "Metastatic malignant neoplasm to conjunctiva (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to conjunctiva", "shortest_name_length": 41}
{"curie": "UMLS:C0855798", "names": ["Stage II Subdiaphragmatic Nodular Sclerosis Hodgkin Lymphoma", "Stage II Subdiaphragmatic Nodular Sclerosis Hodgkin's Disease", "Hodgkin's disease nodular sclerosis stage II subdiaphragmatic", "Stage II Subdiaphragmatic Nodular Sclerosis Hodgkin's Lymphoma", "Stage II Nodular Sclerosis Hodgkin's Disease below the Diaphragm", "Stage II Nodular Sclerosis Hodgkin's Lymphoma below the Diaphragm", "Stage II Subdiaphragmatic Nodular Sclerosis Classical Hodgkin Lymphoma", "Ann Arbor Stage II Subdiaphragmatic Nodular Sclerosis Classic Hodgkin Lymphoma", "Ann Arbor Stage II Subdiaphragmatic Nodular Sclerosis Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's disease nodular sclerosis stage II subdiaphragmatic", "shortest_name_length": 60}
{"curie": "MONDO:0013525", "names": ["CILD16", "primary ciliary dyskinesia 16", "ciliary dyskinesia, primary, 16", "CILIARY DYSKINESIA, PRIMARY, 16", "DNAL1 primary ciliary dyskinesia", "primary ciliary dyskinesia type 16", "ciliary dyskinesia, primary, type 16", "primary ciliary dyskinesia caused by mutation in DNAL1", "primary ciliary dyskinesia 16 with or without situs inversus", "ciliary dyskinesia, primary, 16, with or without situs inversus", "CILIARY DYSKINESIA, PRIMARY, 16, WITH OR WITHOUT SITUS INVERSUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia 16", "shortest_name_length": 6}
{"curie": "MONDO:0003141", "names": ["C-P Angle PNET", "C-P angle PNET", "Cerebellopontine Angle PNET", "cerebellopontine angle PNET", "Cerebellar Pontine Angle PNET", "cerebellar Pontine angle PNET", "cerebellopontine angle embryonal tumor", "C-P angle primitive neuroectodermal tumor", "C-P Angle Primitive Neuroectodermal Tumor", "Cerebellopontine Angle Embryonal Tumor, NOS", "C-P angle primitive neuroectodermal neoplasm", "Primitive Neuroectodermal Tumor of C-P Angle", "C-P Angle Primitive Neuroectodermal Neoplasm", "primitive neuroectodermal tumor of C-P angle", "primitive neuroectodermal neoplasm of C-P angle", "Primitive Neuroectodermal Neoplasm of C-P Angle", "Primitive Neuroectodermal Tumor of the C-P Angle", "cerebellopontine angle primitive neuroectodermal", "primitive neuroectodermal tumor of the C-P angle", "Primitive Neuroectodermal Neoplasm of the C-P Angle", "primitive neuroectodermal neoplasm of the C-P angle", "Cerebellopontine Angle Primitive Neuroectodermal Tumor", "cerebellopontine angle primitive neuroectodermal tumor", "Cerebellar Pontine Angle Primitive Neuroectodermal Tumor", "cerebellar Pontine angle primitive neuroectodermal tumor", "cerebellopontine angle primitive neuroectodermal neoplasm", "Cerebellopontine Angle Primitive Neuroectodermal Neoplasm", "Primitive Neuroectodermal Tumor of Cerebellopontine Angle", "primitive neuroectodermal tumor of cerebellopontine angle", "primitive neuroectodermal tumor of cerebellar Pontine angle", "Cerebellar Pontine Angle Primitive Neuroectodermal Neoplasm", "Primitive Neuroectodermal Tumor of Cerebellar Pontine Angle", "cerebellar Pontine angle primitive neuroectodermal neoplasm", "primitive neuroectodermal neoplasm of cerebellopontine angle", "Primitive Neuroectodermal Neoplasm of Cerebellopontine Angle", "primitive neuroectodermal tumor of the cerebellopontine angle", "Primitive Neuroectodermal Tumor of the Cerebellopontine Angle", "primitive neuroectodermal neoplasm of cerebellar Pontine angle", "Primitive Neuroectodermal Neoplasm of Cerebellar Pontine Angle", "primitive neuroectodermal tumor of the cerebellar Pontine angle", "Primitive Neuroectodermal Tumor of the Cerebellar Pontine Angle", "Cerebellopontine Angle Embryonal Tumor, Not Otherwise Specified", "primitive neuroectodermal neoplasm of the cerebellopontine angle", "Primitive Neuroectodermal Neoplasm of the Cerebellopontine Angle", "Primitive Neuroectodermal Neoplasm of the Cerebellar Pontine Angle", "primitive neuroectodermal neoplasm of the cerebellar Pontine angle"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellopontine angle embryonal tumor", "shortest_name_length": 14}
{"curie": "MONDO:0017175", "names": ["SCA3, Thomas type", "Azorean disease, type II", "azorean disease, type ii", "Machado-Joseph disease type 2", "Azorean disease, type II (disorder)", "spinocerebellar ataxia, Thomas type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Machado-Joseph disease type 2", "shortest_name_length": 17}
{"curie": "MONDO:0001369", "names": ["Laryngitis chronic", "Chronic Laryngitis", "Chronic laryngitis", "Laryngitis;chronic", "chronic laryngitis", "laryngitis chronic", "laryngitis, chronic", "chronic; laryngitis", "LARYNGITIS, CHRONIC", "laryngitis; chronic", "Laryngitis chronic NOS", "Chronic laryngitis, NOS", "Chronic laryngitis (disorder)", "chronic laryngitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic laryngitis", "shortest_name_length": 18}
{"curie": "UMLS:C0278983", "names": ["stage IIIA NSCLC", "Stage IIIA NSCLC", "NSCLC, stage IIIA", "non-oat cell lung cancer, stage IIIA", "stage IIIA nonsmall cell lung cancer", "Lung cancer non-small cell stage IIIA", "stage IIIA non-small cell lung cancer", "lung cancer, non-oat cell, stage IIIA", "Non Small Cell Lung Cancer Stage IIIA", "nonsmall cell lung cancer, stage IIIA", "Non-small cell lung cancer stage IIIA", "Stage IIIA Non-Small Cell Lung Cancer", "lung cancer, nonsmall cell, stage IIIA", "Non Small Cell Lung Cancer, Stage IIIA", "non-small cell lung cancer, stage IIIA", "Stage IIIA Non-Oat Cell Lung Carcinoma", "lung cancer, non-small cell, stage IIIA", "Stage IIIA Non-Small Cell Lung Carcinoma", "Stage IIIA Non-Oat Cell Carcinoma of Lung", "Stage IIIA Non-Small Cell Carcinoma of Lung", "Stage IIIA Non-Small Cell Lung Cancer AJCC v7", "Stage IIIA Non-Oat Cell Carcinoma of the Lung", "Stage IIIA Lung Non-Small Cell Cancer AJCC v7", "Stage IIIA Non-Small Cell Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-small cell lung cancer stage IIIA", "shortest_name_length": 16}
{"curie": "UMLS:C0473575", "names": ["Darier-like epidermal nevus", "Darier-like epidermal naevus", "Acantholytic Dyskeratotic Epidermal Nevi", "Acantholytic Dyskeratotic Epidermal Nevus", "Acantholytic dyskeratotic epidermal nevus", "Acantholytic dyskeratotic epidermal naevus", "ADEN - Acantholytic dyskeratotic epidermal nevus", "ADEN - Acantholytic dyskeratotic epidermal naevus", "Acantholytic dyskeratotic epidermal nevus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acantholytic Dyskeratotic Epidermal Nevus", "shortest_name_length": 27}
{"curie": "UMLS:C0545071", "names": ["nevoid melanoma", "Nevoid melanoma", "Nevoid Melanoma", "Naevoid melanoma", "Minimal deviation melanoma", "Minimal Deviation Melanoma", "minimal deviation melanoma", "MDM - Minimal deviation melanoma", "Nevoid Cutaneous (Skin) Melanoma", "Minimal deviation (nevoid) melanoma", "Minimal Deviation Cutaneous (Skin) Melanoma", "Minimal deviation melanoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Minimal Deviation Melanoma", "shortest_name_length": 15}
{"curie": "UMLS:C0343386", "names": ["C. diff Infection", "C. diff Infections", "CLOSTRIDIA DIFFICILE INFECTION", "Clostridium difficile Infection", "Clostridium difficile infection", "clostridium difficile infection", "clostridium difficile infections", "Clostridium difficile infections", "Infection, Clostridium difficile", "Clostridium difficile Infections", "Clostridioides difficile infection", "Clostridioides difficile (c. diff)", "Clostridioides difficile Infection", "Clostridioides difficile infections", "Infection, Clostridioides difficile", "Clostridium difficile gastroenteritis", "Infection with Clostridioides difficile", "gastroenteritis due to Clostridium difficile", "Infection caused by Clostridioides difficile", "Clostridium difficile gastrointestinal tract infection", "Infection caused by Clostridioides difficile (disorder)", "gastroenteritis due to Clostridium difficile (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clostridium difficile infection", "shortest_name_length": 17}
{"curie": "UMLS:C4684864", "names": ["Refractory Rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Rhabdomyosarcoma", "shortest_name_length": 27}
{"curie": "MONDO:0009094", "names": ["DCCD", "Francois syndrome", "François syndrome", "FRANCOIS SYNDROME", "FranC'ois syndrome", "Francois syndrome (disorder)", "Dermochondrocorneal dystrophy", "dermochondrocorneal dystrophy", "DERMOCHONDROCORNEAL DYSTROPHY", "Dermochondrocorneal dystrophy of François"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermochondrocorneal dystrophy", "shortest_name_length": 4}
{"curie": "MONDO:0012453", "names": ["SPG31", "Spastic Paraplegia 31", "spastic paraplegia 31", "hereditary spastic paraplegia 31", "REEP1 hereditary spastic paraplegia", "hereditary spastic paraplegia type 31", "autosomal dominant spastic paraplegia 31", "Spastic Paraplegia 31, Autosomal Dominant", "SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT", "spastic paraplegia 31, autosomal dominant", "Autosomal dominant spastic paraplegia type 31", "autosomal dominant spastic paraplegia type 31", "familial spastic paraplegia autosomal dominant type 31", "Autosomal dominant spastic paraplegia type 31 (disorder)", "hereditary spastic paraplegia caused by mutation in REEP1", "Autosomal dominant spastic paraplegia type 31 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 31", "shortest_name_length": 5}
{"curie": "MONDO:0001740", "names": ["cornea epidermoid carcinoma", "Cornea Epidermoid Carcinoma", "Corneal Epidermoid Carcinoma", "Corneal Epidermoid carcinoma", "corneal epidermoid carcinoma", "Epidermoid Carcinoma of Cornea", "Cornea Squamous Cell Carcinoma", "cornea squamous cell carcinoma", "epidermoid carcinoma of cornea", "Corneal Squamous Cell Carcinoma", "corneal squamous cell carcinoma", "Squamous cell carcinoma of cornea", "Squamous Cell Carcinoma of Cornea", "squamous cell carcinoma of cornea", "epidermoid carcinoma of the cornea", "Epidermoid Carcinoma of the Cornea", "squamous cell carcinoma of the cornea", "Squamous Cell Carcinoma of the Cornea", "corneal neoplasm squamous cell carcinoma", "Squamous cell carcinoma of cornea (disorder)", "Squamous cell carcinoma of cornea (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cornea squamous cell carcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C0751156", "names": ["FRAXA", "FRAXA Syndrome", "FRAXA Syndromes", "Syndrome, FRAXA", "FRAXA (disorder)", "Syndromes, FRAXA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FRAXA Syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0001380", "names": ["Dome", "BLADDER, DOME", "Dome of Bladder", "Dome of bladder", "bladder dome cancer", "Dome of the Bladder", "Superior Surface of bladder", "superior surface of bladder", "Superior Surface of Bladder", "Superior Surface of the Bladder", "Malignant tumor of bladder dome", "fundus of urinary bladder cancer", "Malignant tumour of bladder dome", "malignant tumor of dome of bladder", "Malignant tumor of vault of bladder", "malignant tumor of vault of bladder", "cancer of fundus of urinary bladder", "Malignant tumour of vault of bladder", "malignant neoplasm of dome of bladder", "Malignant neoplasm of dome of bladder", "Malignant neoplasm of vault of bladder", "malignant fundus of urinary bladder neoplasm", "Malignant neoplasm of apex of urinary bladder", "malignant neoplasm of apex of urinary bladder", "malignant neoplasm of dome of urinary bladder", "Malignant neoplasm of dome of urinary bladder", "Malignant tumor of vault of bladder (disorder)", "malignant neoplasm of fundus of urinary bladder", "malignant neoplasm of dome of bladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder dome cancer", "shortest_name_length": 4}
{"curie": "MONDO:0009088", "names": ["Deafness, Neural, with Atypical Atopic Dermatitis", "DEAFNESS, NEURAL, WITH ATYPICAL ATOPIC DERMATITIS", "deafness, neural, with atypical atopic dermatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness, neural, with atypical atopic dermatitis", "shortest_name_length": 49}
{"curie": "MONDO:0000586", "names": ["exocrine system autoimmune disease", "autoimmune disease of exocrine system", "autoimmune disorder of exocrine system", "exocrine system hypersensitivity reaction type II disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune disorder of exocrine system", "shortest_name_length": 34}
{"curie": "UMLS:C4727579", "names": ["Locally Advanced Sinonasal Squamous Cell Carcinoma", "Locally Advanced Nasal Cavity and Paranasal Sinus Squamous Cell Carcinoma", "Locally Advanced Squamous Cell Carcinoma of the Nasal Cavity and Paranasal Sinus", "Locally Advanced Squamous Cell Carcinoma of the Nasal Cavity and/or Paranasal Sinuses"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Sinonasal Squamous Cell Carcinoma", "shortest_name_length": 50}
{"curie": "MONDO:0024508", "names": ["HWE1", "bathing epilepsy", "hot water epilepsy 1", "Hot Water Epilepsy, 1", "epilepsy, hot water, 1", "EPILEPSY, HOT WATER, 1", "water immersion epilepsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, hot water, 1", "shortest_name_length": 4}
{"curie": "MONDO:0016299", "names": ["holoprosencephaly-caudal dysgenesis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "holoprosencephaly-caudal dysgenesis syndrome", "shortest_name_length": 44}
{"curie": "UMLS:C4682633", "names": ["Stage IVA Fallopian Tube Cancer", "Stage IVA Fallopian Tube Cancer AJCC v8", "Stage IVA Fallopian Tube Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Fallopian Tube Cancer AJCC v8", "shortest_name_length": 31}
{"curie": "UMLS:C0334046", "names": ["Mild", "dysplasia mild", "mild dysplasia", "Mild dysplasia", "Mild Dysplasia", "Mild dysplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mild dysplasia", "shortest_name_length": 4}
{"curie": "MONDO:0011951", "names": ["ALS6", "ALS6 (diagnosis)", "FUS amyotrophic lateral sclerosis", "amyotrophic lateral sclerosis ALS6", "amyotrophic lateral sclerosis type 6", "AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)", "autosomal recessive amyotrophic lateral sclerosis 6", "AMYOTROPHIC LATERAL SCLEROSIS 6, AUTOSOMAL RECESSIVE", "Amyotrophic Lateral Sclerosis 6, Autosomal Recessive", "amyotrophic lateral sclerosis caused by mutation in FUS", "amyotrophic lateral sclerosis 6 with or without frontotemporal dementia", "AMYOTROPHIC LATERAL SCLEROSIS 6 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA", "amyotrophic lateral sclerosis 6, with or without frontotemporal dementia", "Amyotrophic Lateral Sclerosis 6, With or Without Frontotemporal Dementia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyotrophic lateral sclerosis type 6", "shortest_name_length": 4}
{"curie": "UMLS:C3472608", "names": ["Micropapillary carcinoma", "Micropapillary Carcinoma", "Micropapillary Carcinoma, NOS", "Micropapillary Carcinoma, Not Otherwise Specified", "Micropapillary carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Micropapillary carcinoma", "shortest_name_length": 24}
{"curie": "UMLS:C4526976", "names": ["Stage II Small Intestinal, Esophageal, Colorectal, Mesenteric, and Peritoneal GIST AJCC v8", "Stage II Small Intestinal, Esophageal, Colorectal, Mesenteric, and Peritoneal Gastrointestinal Stromal Tumor (GIST)", "Stage II Small Intestinal, Esophageal, Colorectal, Mesenteric, and Peritoneal Gastrointestinal Stromal Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Small Intestinal, Esophageal, Colorectal, Mesenteric, and Peritoneal Gastrointestinal Stromal Tumor AJCC v8", "shortest_name_length": 90}
{"curie": "MONDO:0033551", "names": ["IMD72", "immunodeficiency 72", "immunodeficiency 72 with autoinflammation", "IMMUNODEFICIENCY 72 WITH AUTOINFLAMMATION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 72 with autoinflammation", "shortest_name_length": 5}
{"curie": "MONDO:0012750", "names": ["AAHD", "CAAHD", "LAAHD", "LAAHD, FORMERLY", "Vuopala disease", "Arthrogryposis-anterior horn cell disease syndrome", "lethal arthrogryposis with anterior horn cell disease", "Lethal Arthrogryposis With Anterior Horn Cell Disease", "Lethal arthrogryposis with anterior horn cell disease", "lethal arthrogryposis-anterior horn cell disease syndrome", "CONGENITAL ARTHROGRYPOSIS WITH ANTERIOR HORN CELL DISEASE", "congenital arthrogryposis with anterior horn cell disease", "LETHAL ARTHROGRYPOSIS WITH ANTERIOR HORN CELL DISEASE, FORMERLY", "Lethal arthrogryposis co-occurrent with anterior horn cell disease", "Lethal arthrogryposis co-occurrent with anterior horn cell disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal arthrogryposis-anterior horn cell disease syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0100260", "names": ["PEX2 related Zellweger spectrum disorder", "peroxisome biogenesis disorder due to PEX2 defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder due to PEX2 defect", "shortest_name_length": 40}
{"curie": "MONDO:0006183", "names": ["DPL", "LPD", "Diffuse peritoneal leiomyomatosis", "diffuse peritoneal leiomyomatosis", "Diffuse Peritoneal Leiomyomatosis", "Disseminated peritoneal leiomyomatosis", "Disseminated Peritoneal Leiomyomatosis", "disseminated peritoneal leiomyomatosis", "Leiomyomatosis peritonealis disseminata", "Leiomyomatosis Peritonealis Disseminata", "leiomyomatosis peritonealis disseminata", "leiomyomatosis peritonealis disseminate", "Leiomyomatosis peritonealis disseminate", "Leiomyomatosis, peritonealis disseminata", "Leiomyomatosis peritonealis disseminata (disorder)", "Leiomyomatosis, peritonealis disseminata (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disseminated peritoneal leiomyomatosis", "shortest_name_length": 3}
{"curie": "MONDO:0012901", "names": ["PKK deficiency", "Prekallikrein Deficiency", "prekallikrein deficiency", "Fletcher Factor deficiency", "inherited prekallikrein deficiency", "congenital prekallikrein deficiency", "hereditary prekallikrein deficiency", "prekallikrein deficiency, congenital", "fletcher factor (prekallikrein) deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited prekallikrein deficiency", "shortest_name_length": 14}
{"curie": "UMLS:C5670046", "names": ["Extranodal Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extranodal Non-Hodgkin Lymphoma", "shortest_name_length": 31}
{"curie": "MONDO:0015166", "names": ["AML with t(8;21)(q22;q22) translocation", "acute myeloid leukemia with t(8;21)(q22;q22) translocation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia with t(8;21)(q22;q22) translocation", "shortest_name_length": 39}
{"curie": "UMLS:C4329787", "names": ["Embryonal Tumor with Multilayered Rosettes, NOS", "Embryonal tumor with multilayered rosettes, NOS", "Embryonal Tumor with Multilayered Rosettes without C19MC Alteration", "Embryonal Tumor with Multilayered Rosettes, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Embryonal Tumor with Multilayered Rosettes without C19MC Alteration", "shortest_name_length": 47}
{"curie": "MONDO:0007837", "names": ["JMS", "Aadh syndrome", "AADH syndrome", "AADH SYNDROME", "Johnson-McMillin syndrome", "JOHNSON-MCMILLIN SYNDROME", "Johnson McMillin syndrome", "Johnson-Mcmillin syndrome", "Johnson neuroectodermal syndrome", "JOHNSON NEUROECTODERMAL SYNDROME", "Johnson neuroectodermal syndrome (disorder)", "alopecia anosmia deafness hypogonadism syndrome", "Alopecia-Anosmia-Deafness-Hypogonadism Syndrome", "Alopecia anosmia deafness hypogonadism syndrome", "Alopecia-anosmia-deafness-hypogonadism syndrome", "alopecia-anosmia-deafness-hypogonadism syndrome", "ALOPECIA-ANOSMIA-DEAFNESS-HYPOGONADISM SYNDROME", "Alopecia, anosmia, deafness, hypogonadism syndrome", "alopecia-anosmia-deafness-hypogonadism (AADH) syndrome", "alopecia-anosmia-conductive hearing loss-hypogonadism syndrome", "Alopecia-anosmia-conductive hearing loss-hypogonadism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Johnson neuroectodermal syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0020303", "names": ["UPD(15)pat", "Angelman syndrome due to paternal uniparental disomy of chromosome 15", "Angelman syndrome due to paternal uniparental disomy of chromosome type 15"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Angelman syndrome due to paternal uniparental disomy of chromosome 15", "shortest_name_length": 10}
{"curie": "UMLS:C0730607", "names": ["chronic obstructive pulmonary disease severe", "Severe chronic obstructive pulmonary disease", "Severe chronic obstructive pulmonary disease (disorder)", "Severe chronic obstructive pulmonary disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Severe chronic obstructive pulmonary disease", "shortest_name_length": 44}
{"curie": "MONDO:0007320", "names": ["Familial Apatite disease", "FAMILIAL APATITE DISEASE", "familial apatite disease", "CHONDROCALCINOSIS DUE TO APATITE CRYSTAL DEPOSITION", "chondrocalcinosis due to apatite crystal deposition", "Chondrocalcinosis due to Apatite crystal deposition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chondrocalcinosis due to apatite crystal deposition", "shortest_name_length": 24}
{"curie": "UMLS:C5670724", "names": ["Therapy-Related Cytogenetically Normal Acute Myeloid Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Therapy-Related Cytogenetically Normal Acute Myeloid Leukemia", "shortest_name_length": 61}
{"curie": "UMLS:C2987170", "names": ["Pancreatic Macrocystic Serous Cystadenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Macrocystic Serous Cystadenoma", "shortest_name_length": 41}
{"curie": "MONDO:0007187", "names": ["BCNS", "NBCCS", "Gorlin Syndrome", "GORLIN SYNDROME", "gorlin syndrome", "Gorlin syndrome", "gorlins syndrome", "Syndrome, Gorlin", "gorlin's syndrome", "Gorlin's syndrome", "Gorlin syndrome 2", "gorlins's syndrome", "fifth phacomatosis", "Fifth Phacomatosis", "Fifth Phacomatoses", "Gorlin Goltz Syndrome", "gorlin-goltz syndrome", "gorlin goltz syndrome", "Gorlin-Goltz syndrome", "GORLIN-GOLTZ SYNDROME", "Gorlin-Goltz Syndrome", "Syndrome, Gorlin-Goltz", "basal cell nevus syndrome", "BASAL CELL NEVUS SYNDROME", "basal-cell nevus syndrome", "Basal Cell Nevus Syndrome", "Basal cell nevus syndrome", "Nevus Syndrome, Basal Cell", "Basal cell naevus syndrome", "Gorlin syndrome (disorder)", "basal cell nevus syndrome 1", "basal cell carcinoma syndrome", "Basal cell carcinoma syndrome", "multiple basal cell carcinomas", "Multiple Basal Cell Carcinomas", "BCNS - Basal cell nevus syndrome", "basal-cell nevus syndrome (BCNS)", "BCNS - Basal cell naevus syndrome", "nevoid basal cell cancer syndrome", "Nevoid Basal Cell Cancer Syndrome", "Nevoid basal-cell carcinoma syndrome", "NEVOID BASAL CELL CARCINOMA SYNDROME", "Nevoid basal cell carcinoma syndrome", "nevoid basal cell carcinoma syndrome", "Nevoid Basal Cell Carcinoma Syndrome", "nevoid basal-cell carcinoma syndrome", "Naevoid basal cell carcinoma syndrome", "basal cell nevus syndrome (diagnosis)", "nevoid basal cell carcinoma syndrome 1", "hereditary cutaneomandibular polyoncosis", "NBCCS - Nevoid basal cell carcinoma syndrome", "multiple nevoid basal-cell carcinoma syndrome", "NBCCS - Naevoid basal cell carcinoma syndrome", "multiple hereditary cutaneomandibular polyoncosis", "odontogenic keratocytosis-skeletal anomalies syndrome", "multiple nevoid basal-cell carcinoma syndrome (MNBCCS)", "jaw cysts-basal cell tumors-skeletal anomalies syndrome", "nevoid basal-cell carcinoma (NBCC) syndrome (NBCCS, NBS)", "nevoid basal-cell epithelioma-jaw cysts-bifid rib syndrome", "multiple nevoid basal-cell epithelioma-jaw cysts-bifid rib syndrome", "multiple basal-cell carcinoma syndrome multiple basal-cell nevus syndrome", "multiple basal cell nevi, odontogenic keratocysts, and skeletal anomalies", "Multiple Basal Cell Nevi, Odontogenic Keratocysts, and Skeletal Anomalies", "MULTIPLE BASAL CELL NEVI, ODONTOGENIC KERATOCYSTS, AND SKELETAL ANOMALIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nevoid basal cell carcinoma syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0005479", "names": ["Atrial Tachycardia", "atrial tachycardia", "TACHYCARDIA ATRIAL", "ATRIAL TACHYCARDIA", "Tachycardia atrial", "tachycardia atrial", "Atrial tachycardia", "atrium; tachycardia", "tachycardia; atrial", "atrial tachycardias", "auricular; tachycardia", "tachycardia; auricular", "Atrial tachycardia, NOS", "Atrial tachycardia (disorder)", "atrial tachycardia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial tachycardia", "shortest_name_length": 18}
{"curie": "MONDO:0024357", "names": ["Drug induced central sleep apnea", "drug induced central sleep apnea", "Drug induced central sleep apnoea", "Drug induced central sleep apnea (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "drug induced central sleep apnea", "shortest_name_length": 32}
{"curie": "MONDO:0041526", "names": ["abortion", "Abortion", "ABORTION", "ABORTIONS", "Abortions", "abortions", "ABORTION NOS", "Abortion NOS", "Abortion, NOS", "Pregnancy Loss", "Abortion Finding", "Unspecified abortion", "abortion (diagnosis)", "Unspecified Abortion", "miscarriage or abortion", "Pregnancy with abortive outcome", "pregnancy with abortive outcome", "pregnancy resulting in fetal death", "pregnancy disorder with abortive outcome", "Pregnancy with abortive outcome (O00-O08)", "Pregnancy with abortive outcome (disorder)", "Pregnancy with abortive outcome (diagnosis)", "pregnancy complications with abortive outcome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pregnancy disorder with abortive outcome", "shortest_name_length": 8}
{"curie": "MONDO:0030677", "names": ["CMT1I", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 1I", "Charcot-Marie-Tooth disease neuropathy, IIA 1I", "Charcot-Marie-Tooth disease, demyelinating, IIA 1I", "CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease, demyelinating, IIA 1I", "shortest_name_length": 5}
{"curie": "MONDO:0016735", "names": ["PGNT", "papillary glioneuronal tumor", "Papillary glioneuronal tumor", "Papillary Glioneuronal Tumor", "Papillary glioneuronal tumour", "Pseudopapillary ganglioglioneurocytoma", "pseudopapillary ganglioglioneurocytoma", "Papillary Glioneuronal Tumor (WHO Grade 1)", "papillary glioneuronal tumor (WHO grade I)", "Papillary Glioneuronal Tumor (WHO Grade I)", "Papillary glioneuronal tumor (morphologic abnormality)", "Pseudopapillary neurocytoma with glial differentiation", "pseudopapillary neurocytoma with glial differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papillary glioneuronal tumor", "shortest_name_length": 4}
{"curie": "UMLS:C4525353", "names": ["III", "Stage III Intrahepatic Cholangiocarcinoma AJCC v8", "Stage III Intrahepatic Bile Duct Cancer (Cholangiocarcinoma)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Intrahepatic Cholangiocarcinoma AJCC v8", "shortest_name_length": 3}
{"curie": "MONDO:0023603", "names": ["heritable connective tissue disorder", "Mendelian connective tissue disorder", "Connective Tissue Hereditary Disorder", "connective tissue hereditary disorder", "hereditary connective tissue disorder", "Hereditary Connective Tissue Disorder", "Connective tissue hereditary disorder", "inherited disorder of connective tissue", "Inherited disorder of connective tissue", "hereditary disorder of connective tissue", "Connective tissue hereditary disorder (disorder)", "inherited disorder of connective tissue (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary disorder of connective tissue", "shortest_name_length": 36}
{"curie": "MONDO:0013973", "names": ["ECTD5", "ectodermal dysplasia 5", "ectodermal dysplasia 5, hair/nail type", "ECTODERMAL DYSPLASIA 5, HAIR/NAIL TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia 5, hair/nail type", "shortest_name_length": 5}
{"curie": "MONDO:0015072", "names": ["HNEC", "PHNEC", "Liver Neuroendocrine Cancer", "liver neuroendocrine cancer", "liver neuroendocrine carcinoma", "Liver Neuroendocrine Carcinoma", "hepatic neuroendocrine carcinoma", "Hepatic Neuroendocrine Carcinoma", "neuroendocrine carcinoma of liver", "Liver Neuroendocrine Carcinoma, NOS", "primary liver neuroendocrine carcinoma", "Primary Liver Neuroendocrine Carcinoma", "Primary hepatic neuroendocrine carcinoma", "primary hepatic neuroendocrine carcinoma", "Primary Hepatic Neuroendocrine Carcinoma", "Primary hepatic neuroendocrine carcinoma (disorder)", "Liver Neuroendocrine Carcinoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "liver neuroendocrine carcinoma", "shortest_name_length": 4}
{"curie": "UMLS:C1135773", "names": ["Nervous System Acquired Metabolic Diseases", "Acquired Metabolic Diseases, Nervous System", "Metabolic Diseases, Acquired, Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired Metabolic Diseases, Nervous System", "shortest_name_length": 42}
{"curie": "UMLS:C5446385", "names": ["Lacrimal Gland Oncocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lacrimal Gland Oncocytoma", "shortest_name_length": 25}
{"curie": "UMLS:C0151618", "names": ["EMBOLUS LEG", "Embolus leg", "embolism; leg", "leg; embolism", "EMBOLUS LOWER EXTREMITY", "Embolus lower extremity", "lower extremity; embolism", "embolism; lower extremity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Embolus leg", "shortest_name_length": 11}
{"curie": "MONDO:0005559", "names": ["neurodegeneration", "Neurodegeneration", "nerve degeneration", "brain degeneration", "Nerve degeneration", "Nerve Degeneration", "neural degeneration", "Neuron Degeneration", "Nerve Degenerations", "degeneration neuron", "neuron degeneration", "degeneration nerves", "Degeneration, Nerve", "Neuron Degenerations", "degenerative disease", "Degeneration, Neuron", "degeneration neurons", "Degenerations, Nerve", "Degenerative disease", "Degenerative Disease", "Degenerative Disorder", "Degenerative disorder", "Degenerations, Neuron", "degenerative disorder", "degenerative disorders", "cns degenerative disease", "CNS degenerative disease", "neurodegenerative disease", "Neurodegenerative Disease", "Neurodegenerative disease", "cns degenerative diseases", "CNS degenerative disorder", "disease neurodegenerative", "diseases neurodegenerative", "Neurodegenerative Disorder", "NEURODEGENERATIVE DISORDER", "cns degenerative disorders", "Neurodegenerative diseases", "Neurodegenerative Diseases", "Neuro-degenerative disease", "neurodegenerative disorder", "neurodegenerative diseases", "Neurodegenerative disorder", "Neurodegenerative Disorders", "neurodegenerative disorders", "Ongoing loss of nerve cells", "cerebral degeneration disease", "Neurologic Degenerative Disease", "Degenerative Neurologic Disease", "Degenerative Neurologic Disorder", "Neurologic Degenerative Diseases", "degenerative neurologic diseases", "Degenerative disorder (disorder)", "degenerative neurologic disorder", "Neurologic Disease, Degenerative", "Degenerative Neurologic Diseases", "Neurologic Degenerative Condition", "degenerative disorder (diagnosis)", "Degenerative Neurologic Disorders", "degenerative disorders neurologic", "Neurologic Diseases, Degenerative", "Neurologic Disorder, Degenerative", "Degenerative Diseases, Neurologic", "Neurologic Disorders, Degenerative", "Neurologic Degenerative Conditions", "Degenerative Condition, Neurologic", "degenerative disease nervous system", "Degenerative Conditions, Neurologic", "Nervous System Degenerative Diseases", "Degenerative Diseases, Nervous System", "degenerative disease of nervous system", "Progressive neurodegenerative disorder", "Central Nervous System Degenerative Disorder", "central nervous system degenerative disorder", "Degenerative Diseases, Central Nervous System", "degenerative disorder of central nervous system", "central nervous system neurodegenerative disorder", "Central Nervous System Neurodegenerative Disorder", "degenerative disease of nervous system (diagnosis)", "Degenerative disease of the central nervous system", "Degenerative disease or syndrome of nervous system", "Degenerative disease of nervous system, unspecified", "Degenerative Diseases and Syndromes of Nervous System", "Degenerative disease of the central nervous system, NOS", "Degenerative disease of the central nervous system (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodegenerative disease", "shortest_name_length": 17}
{"curie": "UMLS:C0677701", "names": ["Stage II Grade 1 Follicular Lymphoma", "noncontiguous stage II grade 1 follicular lymphoma", "Stage II Grade 1 Non-Contiguous Follicular Lymphoma", "Non-Contiguous Grade I Follicular Lymphoma Stage II", "Non-Contiguous Stage II Grade I Follicular Lymphoma", "Ann Arbor Stage II Grade 1 Non-Contiguous Follicular Lymphoma", "Stage II Non-Contiguous Follicular Small Cleaved Cell Lymphoma", "Non-Contiguous Follicular Small Cleaved Cell Lymphoma Stage II", "Non-Contiguous Stage II Follicular Small Cleaved Cell Lymphoma", "noncontiguous stage II grade I follicular small cleaved cell lymphoma", "Non-Contiguous Grade I Follicular Small Cleaved Cell Lymphoma Stage II", "Non-Contiguous Stage II Grade I Follicular Small Cleaved Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage II Grade 1 Non-Contiguous Follicular Lymphoma", "shortest_name_length": 36}
{"curie": "MONDO:0011363", "names": ["T2D3", "NIDDM3", "TYPE 2 DIABETES MELLITUS 3", "type 2 diabetes mellitus 3", "Noninsulin-Dependent Diabetes Mellitus 3", "NONINSULIN-DEPENDENT DIABETES MELLITUS 3", "noninsulin-dependent diabetes mellitus 3", "DIABETES MELLITUS, NONINSULIN-DEPENDENT, 3", "diabetes mellitus, noninsulin-dependent, 3", "Diabetes Mellitus, Noninsulin-Dependent, 3", "diabetes mellitus, noninsulin-dependent, type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diabetes mellitus, noninsulin-dependent, 3", "shortest_name_length": 4}
{"curie": "MONDO:0025514", "names": ["White atrophy", "White Atrophy", "white atrophy", "Livedo Vasculitis", "livedo vasculitis", "Vasculitis, Livedo", "Livedo Vasculitides", "Livedoid vasculitis", "vasculitis livedoid", "Livedoid Vasculitis", "livedoid vasculitis", "Vasculitis, Livedoid", "livedoid vasculopathy", "Livedoid vasculopathy", "Livedoid Vasculopathy", "Vasculopathy, Livedoid", "Livedoid Vasculopathies", "Milian atrophie blanche", "idiopathic atrophic blanche", "Idiopathic Atrophic Blanche", "Idiopathic atrophic blanche", "Atrophic Blanche, Idiopathic", "Blanches, Idiopathic Atrophic", "Livedoid vasculitis (diagnosis)", "Segmental hyalinizing vasculitis", "segmental hyalinizing vasculopathy", "Livedo Reticularis with Summer Ulceration", "livedo reticularis with summer ulcerations", "Livedo reticularis with summer ulcerations", "livedo reticularis with winter ulcerations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "livedoid vasculopathy", "shortest_name_length": 13}
{"curie": "UMLS:C0338758", "names": ["episodic cannabis dependence", "Cannabis dependence, episodic", "Cannabis dependence, episodic use", "Cannabis Dependence, Episodic Use", "episodic cannabis dependence (diagnosis)", "Cannabis dependence, episodic (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cannabis dependence, episodic", "shortest_name_length": 28}
{"curie": "UMLS:C5668148", "names": ["Invasive Lung Non-Mucinous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Invasive Lung Non-Mucinous Adenocarcinoma", "shortest_name_length": 41}
{"curie": "UMLS:C0586372", "names": ["Moderate Rectal Dysplasia", "Moderate Dysplasia of Rectum", "Moderate dysplasia of rectum", "Moderate Dysplasia of the Rectum", "Moderate dysplasia of rectum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Moderate dysplasia of rectum", "shortest_name_length": 25}
{"curie": "MONDO:0030991", "names": ["BACD1", "BILE ACID CONJUGATION DEFECT 1", "bile acid conjugation defect 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bile acid conjugation defect 1", "shortest_name_length": 5}
{"curie": "UMLS:C5204263", "names": ["Renal Lymphangioma", "Kidney Lymphangioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kidney Lymphangioma", "shortest_name_length": 18}
{"curie": "MONDO:0015653", "names": ["monogenic epilepsy", "monogenic disease with epilepsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "monogenic epilepsy", "shortest_name_length": 18}
{"curie": "MONDO:0001433", "names": ["vaginosis", "disease vagina", "vagina disease", "disease vaginal", "diseases vagina", "Vaginal Disease", "vaginal disease", "vagina disorder", "Vaginal Disorder", "vaginal diseases", "Vagina--Diseases", "Disease, Vaginal", "Vaginal disorder", "disorders vagina", "diseases vaginal", "vaginal disorder", "Vaginal Diseases", "Diseases, Vaginal", "disease of vagina", "diseases vaginals", "disorders vaginal", "Disorder of vagina", "disorder of vagina", "Vaginal disorder NOS", "Vaginal disorder, NOS", "disease of the vagina", "Disease of vagina, NOS", "vagina disease or disorder", "vaginal disorder (diagnosis)", "disease or disorder of vagina", "Disorder of vagina (disorder)", "disease (or disorder); vagina"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vaginal disorder", "shortest_name_length": 9}
{"curie": "MONDO:0033480", "names": ["SCA45", "spinocerebellar ataxia 45", "SPINOCEREBELLAR ATAXIA 45", "Spinocerebellar ataxia type 45"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia 45", "shortest_name_length": 5}
{"curie": "UMLS:C1333108", "names": ["Colorectal Adenoma with Severe Dysplasia", "Colorectal Adenoma with Marked Dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Adenoma with Severe Dysplasia", "shortest_name_length": 40}
{"curie": "MONDO:0015007", "names": ["SINO", "SINO syndrome", "spastic paraplegia, intellectual disability, nystagmus, and obesity", "SPASTIC PARAPLEGIA, INTELLECTUAL DISABILITY, NYSTAGMUS, AND OBESITY", "spastic paraplegia, intellectual disability, nystagmus, and obesity;", "Spastic paraplegia-intellectual disability-nystagmus-obesity syndrome", "Spastic paraplegia, intellectual disability, nystagmus, obesity syndrome", "Spastic paraplegia, intellectual disability, nystagmus, obesity syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic paraplegia, intellectual disability, nystagmus, and obesity;", "shortest_name_length": 4}
{"curie": "MONDO:0015534", "names": ["JXG", "Juvenile xanthoma", "juvenile xanthoma", "Juvenile Xanthoma", "Xanthoma multiplex", "Xanthoma, Juvenile", "xanthoma neviforme", "Xanthoma neviforme", "Juvenile Xanthomas", "Xanthoma naeviforme", "Xanthomas, Juvenile", "Nevoid histiocytoma", "Nevoxanthoendothelioma", "nevoxanthoendothelioma", "Nevoxanthoendotheliomas", "Naevoxanthoendothelioma", "Juvenile Xanthogranuloma", "juvenile xanthogranuloma", "Juvenile xanthogranuloma", "xanthogranuloma juvenile", "juvenile xanthogranulomas", "Xanthogranuloma, Juvenile", "Xanthogranuloma, juvenile", "Juvenile Xanthogranulomas", "Xanthogranulomas, Juvenile", "Juvenile giant cell granuloma", "Congenital xanthoma tuberosum", "JXG - Juvenile xanthogranuloma", "Juvenile Solitary Xanthogranuloma", "Juvenile xanthogranuloma (disorder)", "Multiple eruptive xanthoma in infancy", "Multiple eruptive juvenile xanthogranuloma", "multiple eruptive juvenile xanthogranuloma", "Multiple eruptive juvenile xanthogranuloma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile xanthogranuloma", "shortest_name_length": 3}
{"curie": "UMLS:C4520720", "names": ["stage IIIB anal cancer", "Stage IIIB Anal Canal Cancer", "Stage IIIB Anal Canal Cancer AJCC v7", "Stage IIIB Anal Canal Cancer AJCC v6", "Stage IIIB Anal Carcinoma AJCC v6 and v7", "Stage IIIB Anal Canal Cancer AJCC v6 and v7", "Stage IIIB Anal Canal Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Anal Canal Cancer AJCC v6 and v7", "shortest_name_length": 22}
{"curie": "MONDO:0014694", "names": ["SCDO6", "spondylocostal dysostosis 6", "autosomal recessive spondylocostal dysostosis 6", "spondylocostal dysostosis 6, autosomal recessive", "SPONDYLOCOSTAL DYSOSTOSIS 6, AUTOSOMAL RECESSIVE", "RIPPLY2 autosomal recessive spondylocostal dysostosis", "autosomal recessive spondylocostal dysostosis caused by mutation in RIPPLY2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondylocostal dysostosis 6, autosomal recessive", "shortest_name_length": 5}
{"curie": "MONDO:0009405", "names": ["Cervical hypertrichosis neuropathy", "cervical hypertrichosis peripheral neuropathy", "cervical hypertrichosis-peripheral neuropathy syndrome", "Hypertrichosis, Congenital Anterior Cervical, with Peripheral Sensory and Motor Neuropathy", "HYPERTRICHOSIS, CONGENITAL ANTERIOR CERVICAL, WITH PERIPHERAL SENSORY AND MOTOR NEUROPATHY", "hypertrichosis, congenital anterior cervical, with peripheral sensory and motor neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical hypertrichosis-peripheral neuropathy syndrome", "shortest_name_length": 34}
{"curie": "MONDO:0014577", "names": ["SRTD13", "short-rib thoracic dysplasia 13 with or without polydactyly", "SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short-rib thoracic dysplasia 13 with or without polydactyly", "shortest_name_length": 6}
{"curie": "MONDO:0005811", "names": ["infectious myxomatosis", "Infectious Myxomatoses", "Infectious Myxomatosis", "Myxomatosis, Infectious", "Myxomatoses, Infectious"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infectious myxomatosis", "shortest_name_length": 22}
{"curie": "MONDO:0011958", "names": ["bile and pancreatic ducts, complete absence of", "BILE AND PANCREATIC DUCTS, COMPLETE ABSENCE OF", "Bile and Pancreatic Ducts, Complete Absence of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bile and pancreatic ducts, complete absence of", "shortest_name_length": 46}
{"curie": "MONDO:0018021", "names": ["hypotrichosis-deafness syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotrichosis-deafness syndrome", "shortest_name_length": 31}
{"curie": "MONDO:0017046", "names": ["neuroepithelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuroepithelioma", "shortest_name_length": 16}
{"curie": "UMLS:C0342219", "names": ["Hypoglucagonemia", "hypoglucagonemia", "Hypoglucagonaemia", "Glucagon deficiency", "glucagon deficiency", "Glucagon Deficiency", "Depleted glucagon secretion", "Glucagon deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Glucagon deficiency", "shortest_name_length": 16}
{"curie": "MONDO:0018110", "names": ["lethal idiopathic viral infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal idiopathic viral infection", "shortest_name_length": 33}
{"curie": "MONDO:0001714", "names": ["BEJEL", "bejel", "Bejel", "Frenga", "Bejels", "Njovera", "Dichuchwa", "Endemic syphilis", "Bejel (disorder)", "endemic syphilis", "Bejel (diagnosis)", "nonvenereal syphilis", "Non-venereal syphilis", "Nonvenereal endemic syphilis", "nonvenereal endemic syphilis", "Treponema pallidum subsp. endemicum infectious disease", "Treponema pallidum subsp. endemicum disease or disorder", "Treponema pallidum subsp. endemicum caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bejel", "shortest_name_length": 5}
{"curie": "MONDO:0032604", "names": ["RP84", "retinitis pigmentosa 84", "RETINITIS PIGMENTOSA 84"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 84", "shortest_name_length": 4}
{"curie": "UMLS:C1168327", "names": ["HGPIN", "High-Grade PIN", "High grade prostatic intraepithelial neoplasia", "high grade prostatic intraepithelial neoplasia", "High Grade Prostatic Intraepithelial Neoplasia", "High-Grade Intraepithelial Neoplasia of Prostate", "High-Grade Intraepithelial Neoplasia of the Prostate", "High-grade Prostatic Intraepithelial Neoplasia (PIN)", "high grade prostatic intraepithelial neoplasia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Prostatic Intraepithelial Neoplasia", "shortest_name_length": 5}
{"curie": "UMLS:C3899377", "names": ["Digestive System Hemorrhage", "Hemorrhage of digestive system", "Haemorrhage of digestive system", "Hemorrhage of digestive system (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemorrhage of digestive system", "shortest_name_length": 27}
{"curie": "MONDO:0006791", "names": ["Hyperemesis", "pregnancy hyperemesis", "hyperemesis pregnancy", "gravidarum hyperemesis", "Hyperemesis gravidarum", "Hyperemesis Gravidarum", "HYPEREMESIS GRAVIDARUM", "hyperemesis gravidarum", "gravidarum; hyperemesis", "hyperemesis; gravidarum", "hyperemesis in pregnancy", "hyperemesis of pregnancy", "Hyperemesis in pregnancy", "Hyperemesis of pregnancy", "Excess vomiting in pregnancy", "Excessive pregnancy vomiting", "excessive vomiting pregnancy", "Pregnancy Pernicious Vomiting", "pregnancy pernicious vomiting", "excessive vomiting in pregnancy", "Excessive vomiting in pregnancy", "Pernicious Vomiting of Pregnancy", "hyperemesis gravidarum (disease)", "pernicious vomiting of pregnancy", "VOMITING, PERNICIOUS, OF PREGNANCY", "hyperemesis gravidarum (diagnosis)", "Hyperemesis arising during pregnancy", "Excessive vomiting in pregnancy (disorder)", "Persistent or vicious vomiting arising during pregnancy", "Persistent AND/OR vicious vomiting arising during pregnancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperemesis gravidarum", "shortest_name_length": 11}
{"curie": "MONDO:0007161", "names": ["ASG", "SPGF2", "ASPERMIOGENESIS FACTOR", "Aspermiogenesis Factor", "spermatogenic failure 2", "SPERMATOGENIC FAILURE 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 2", "shortest_name_length": 3}
{"curie": "UMLS:C1332481", "names": ["Benign CNS Soft Tissue Tumor", "Benign CNS Soft Tissue Neoplasm", "Benign Soft Tissue Tumor of CNS", "Benign Soft Tissue Neoplasm of CNS", "Benign Soft Tissue Tumor of the CNS", "Benign Soft Tissue Neoplasm of the CNS", "Benign Central Nervous System Soft Tissue Tumor", "Benign Central Nervous System Soft Tissue Neoplasm", "Benign Soft Tissue Tumor of Central Nervous System", "Benign Soft Tissue Neoplasm of Central Nervous System", "Benign Soft Tissue Tumor of the Central Nervous System", "Benign Soft Tissue Neoplasm of the Central Nervous System", "Benign Central Nervous System Mesenchymal, Non-Meningothelial Tumor", "Benign Central Nervous System Mesenchymal, Non-Meningothelial Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Central Nervous System Mesenchymal, Non-Meningothelial Neoplasm", "shortest_name_length": 28}
{"curie": "UMLS:C1708565", "names": ["Invasive Melanoma", "Infiltrating Melanoma", "Invasive Skin Melanoma", "Invasive Cutaneous Melanoma", "Invasive Cutaneous (Skin) Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Invasive Cutaneous Melanoma", "shortest_name_length": 17}
{"curie": "MONDO:0011616", "names": ["HPE6", "HOLOPROSENCEPHALY 6", "Holoprosencephaly 6", "holoprosencephaly 6", "holoprosencephaly type 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "holoprosencephaly 6", "shortest_name_length": 4}
{"curie": "MONDO:0013008", "names": ["IMD10", "STIM1 deficiency", "STIM1 DEFICIENCY", "IMMUNODEFICIENCY 10", "immunodeficiency 10", "immunodeficiency type 10", "CID due to STIM1 deficiency", "combined immunodeficiency due to STIM1 deficiency", "Combined immunodeficiency due to STIM1 deficiency", "immune dysfunction with T-cell inactivation due to calcium entry defect 2", "IMMUNE DYSFUNCTION WITH T-CELL INACTIVATION DUE TO CALCIUM ENTRY DEFECT 2", "Immune dysfunction with T-cell inactivation due to calcium entry defect 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined immunodeficiency due to STIM1 deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0018574", "names": ["intellectual disability-expressive aphasia-facial dysmorphism syndrome", "intellectual disability-loss of expressive language-facial dysmorphism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability-expressive aphasia-facial dysmorphism syndrome", "shortest_name_length": 70}
{"curie": "MONDO:0017292", "names": ["WDFA", "fetal adenocarcinoma", "Fetal adenocarcinoma", "Fetal Adenocarcinoma", "Foetal adenocarcinoma", "Fetal Lung Adenocarcinoma", "Lung Fetal Adenocarcinoma", "fetal lung adenocarcinoma", "Fetal adenocarcinoma of lung", "Foetal adenocarcinoma of lung", "lung malignant adenocarcinoma fetal", "Pulmonary Adenocarcinoma of Fetal Type", "pulmonary adenocarcinoma of fetal type", "Fetal adenocarcinoma of lung (disorder)", "Fetal adenocarcinoma of lung (diagnosis)", "well-differentiated fetal lung adenocarcinoma", "Well-Differentiated Fetal Lung Adenocarcinoma", "Fetal adenocarcinoma (morphologic abnormality)", "Pulmonary Endodermal Tumor Resembling Fetal Lung", "pulmonary endodermal tumor resembling fetal lung", "well-differentiated fetal adenocarcinoma of the lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "well-differentiated fetal adenocarcinoma of the lung", "shortest_name_length": 4}
{"curie": "MONDO:0000141", "names": ["MVA1", "MVA SYNDROME", "MVA Syndrome", "Warburton Anyane Yeboa syndrome", "Warburton-Anyane-Yeboa syndrome", "Mosaic variegated aneuploidy syndrome", "mosaic variegated aneuploidy syndrome", "Mosaic variegated aneuploidy syndrome 1", "Mosaic Variegated Aneuploidy Syndrome 1", "MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1", "Instability mitotic non disjunction syndrome", "Mosaic variegated aneuploidy syndrome (disorder)", "Mosaic variegated aneuplody microcephaly syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mosaic variegated aneuploidy syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C4524524", "names": ["Stage IV", "Stage IV Head and Neck Squamous Cell Cancer", "Stage IV Cutaneous Squamous Cell Carcinoma of the Head and Neck AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Cutaneous Squamous Cell Carcinoma of the Head and Neck AJCC v8", "shortest_name_length": 8}
{"curie": "MONDO:0012398", "names": ["RCD3A", "ACHM6", "achromatopsia 6", "ACHROMATOPSIA 6", "retinal cone dystrophy 3", "retinal cone dystrophy 3A", "Retinal Cone Dystrophy 3A", "RETINAL CONE DYSTROPHY 3A", "retinal cone dystrophy type 3A", "cone dystrophy with night blindness and supernormal rod responses PDE6H-related", "Cone Dystrophy with Night Blindness and Supernormal Rod Responses, PDE6H-Related", "CONE DYSTROPHY WITH NIGHT BLINDNESS AND SUPERNORMAL ROD RESPONSES, PDE6H-RELATED", "cone dystrophy with night blindness and supernormal Rod responses, Pde6H-related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal cone dystrophy 3A", "shortest_name_length": 5}
{"curie": "MONDO:0023290", "names": ["grix Blankenship Peterson syndrome", "craniofacial and osseous defects mental retardation", "craniofacial and osseous defects intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "grix Blankenship Peterson syndrome", "shortest_name_length": 34}
{"curie": "MONDO:0100267", "names": ["PEX13 related Zellweger spectrum disorder", "peroxisome biogenesis disorder due to PEX13 defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder due to PEX13 defect", "shortest_name_length": 41}
{"curie": "MONDO:0031199", "names": ["inherited interstitial lung disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited interstitial lung disease", "shortest_name_length": 35}
{"curie": "UMLS:C0863189", "names": ["Stomach carcinoma stage II", "Gastric carcinoma stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric carcinoma stage II", "shortest_name_length": 26}
{"curie": "MONDO:0015550", "names": ["suprabasal epidermolysis bullosa simplex", "Suprabasal epidermolysis bullosa simplex", "Suprabasal epidermolysis bullosa simplex (disorder)", "epidermis suprabasal layer epidermolysis bullosa simplex", "epidermolysis bullosa simplex of epidermis suprabasal layer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "suprabasal epidermolysis bullosa simplex", "shortest_name_length": 40}
{"curie": "MONDO:0023138", "names": ["Feingold trainer syndrome", "Feingold Trainer syndrome", "Unusual facies, cleft palate, short stature, and mental retardation", "unusual facies, cleft palate, short stature, and mental retardation", "unusual facies, cleft palate, short stature, and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Feingold trainer syndrome", "shortest_name_length": 25}
{"curie": "UMLS:C4763633", "names": ["Islet Glucagon Cell Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Islet Glucagon Cell Hyperplasia", "shortest_name_length": 31}
{"curie": "UMLS:C5419192", "names": ["Metastatic Unclassified Renal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Unclassified Renal Cell Carcinoma", "shortest_name_length": 44}
{"curie": "MONDO:0011683", "names": ["OCA4", "Oculocutaneous albinism type 4", "oculocutaneous albinism type 4", "oculocutaneous albinism type IV", "SLC45A2 oculocutaneous albinism", "Oculocutaneous albinism, type 4", "oculocutaneous albinism, type 4", "OCULOCUTANEOUS ALBINISM, TYPE IV", "Oculocutaneous Albinism, Type IV", "albinism, oculocutaneous, type 4", "Albinism, Oculocutaneous, Type IV", "ALBINISM, OCULOCUTANEOUS, TYPE IV", "albinism, oculocutaneous, type IV", "Oculocutaneous albinism type 4 (disorder)", "oculocutaneous albinism type 4 (diagnosis)", "oculocutaneous albinism caused by mutation in SLC45A2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculocutaneous albinism type 4", "shortest_name_length": 4}
{"curie": "UMLS:C4726551", "names": ["Myeloid Neoplasms with Germline Predisposition Associated with Other Organ Dysfunction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myeloid Neoplasms with Germline Predisposition Associated with Other Organ Dysfunction", "shortest_name_length": 86}
{"curie": "UMLS:C1266016", "names": ["Enteroglucagonoma", "Enteroglucagonoma, NOS", "Enteroglucagonoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Enteroglucagonoma", "shortest_name_length": 17}
{"curie": "MONDO:0019463", "names": ["Randall disease", "non-amyloid MIDD", "non-amyloid monoclonal immunoglobulin deposition disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-amyloid monoclonal immunoglobulin deposition disease", "shortest_name_length": 15}
{"curie": "MONDO:0010404", "names": ["SCAX5", "Scax5", "X-linked spinocerebellar ataxia 5", "Spinocerebellar Ataxia, X-Linked 5", "SPINOCEREBELLAR ATAXIA, X-LINKED 5", "spinocerebellar ataxia, X-linked 5", "X-linked spinocerebellar ataxia type 5", "X-linked non progressive cerebellar ataxia", "X-linked non progressive cerebellar ataxia (disorder)", "spinocerebellar ataxia, X-linked 5, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked non progressive cerebellar ataxia", "shortest_name_length": 5}
{"curie": "MONDO:0014667", "names": ["MC4DN9", "CEMCOX3", "COA5 fatal infantile encephalocardiomyopathy", "mitochondrial complex IV deficiency nuclear type 9", "MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 9", "mitochondrial complex IV, deficiency, nuclear type 9", "fatal infantile encephalocardiomyopathy caused by mutation in COA5", "fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 3", "CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 3", "cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3", "cardioencephalomyopathy, fatal infantile, due to cytochrome C oxidase deficiency type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3", "shortest_name_length": 6}
{"curie": "MONDO:0018996", "names": ["AOA2", "SCAN2", "SCAR1", "SCAN 2", "SCAR1, FORMERLY", "ataxia-ocular apraxia 2", "Ataxia-ocular apraxia 2", "ATAXIA-OCULAR APRAXIA 2", "Ataxia-oculomotor apraxia 2", "ATAXIA-OCULOMOTOR APRAXIA 2", "ataxia-oculomotor apraxia 2", "Ataxia with Oculomotor Apraxia", "ataxia-oculomotor apraxia type 2", "Ataxia-oculomotor apraxia type 2", "Ataxia with Oculomotor Apraxia Type 2", "ataxia with oculomotor apraxia type 2", "Ataxia  with Oculomotor Apraxia Type 2", "AOA2 - ataxia oculomotor apraxia type 2", "autosomal recessive spinocerebellar ataxia-1", "spinocerebellar ataxia, autosomal recessive 1", "Spinocerebellar ataxia, autosomal recessive 1", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1", "spinocerebellar ataxia, autosomal recessive type 1", "Spinocerebellar ataxia with axonal neuropathy type 2", "SCAR1 - spinocerebellar ataxia autosomal recessive 1", "spinocerebellar ataxia with axonal neuropathy type 2", "Spinocerebellar Ataxia with Axonal Neuropathy Type 2", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1, FORMERLY", "Spinocerebellar Ataxia, Recessive, Non-Friedreich Type 1", "Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2", "Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy 2", "spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE, WITH AXONAL NEUROPATHY 2", "Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2", "shortest_name_length": 4}
{"curie": "UMLS:C2348509", "names": ["Fascicular Tachycardia", "Fascicular Tachycardia by ECG Finding", "Fascicular Tachycardia by EKG Finding"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fascicular Tachycardia by ECG Finding", "shortest_name_length": 22}
{"curie": "MONDO:0006983", "names": ["Basilar Steal Syndrome", "Steal Syndrome, Basilar", "Basilar Steal Syndromes", "Steal Syndromes, Basilar", "Subclavian steal syndrome", "steal subclavian syndrome", "Subclavian Steal Syndrome", "subclavian steal syndrome", "SUBCLAVIAN STEAL SYNDROME", "SUBCLAVIAN ARTERY STENOSIS", "subclavian artery stenosis", "Steal Syndrome, Subclavian", "subclavian steal; syndrome", "Subclavian artery stenosis", "Subclavian Artery Stenoses", "Subclavian Steal Syndromes", "artery stenosis subclavian", "syndrome; subclavian steal", "Subclavian Artery Stenosis", "Stenosis, Subclavian Artery", "Artery Stenoses, Subclavian", "Stenoses, Subclavian Artery", "Steal Syndromes, Subclavian", "subclavian steal phenomenon", "Artery Stenosis, Subclavian", "stenosis of subclavian artery", "Subclavian steal syndrome (disorder)", "Subclavian artery stenosis (disorder)", "subclavian steal syndrome (diagnosis)", "Brachial-Basilar Insufficiency Syndrome", "Brachial Basilar Insufficiency Syndrome", "BRACHIAL-BASILAR INSUFFICIENCY SYNDROME", "Insufficiency Syndrome, Brachial-Basilar", "subclavian steal steno-occlusive disease", "Brachial-Basilar Insufficiency Syndromes", "Syndrome, Brachial-Basilar Insufficiency", "Insufficiency Syndromes, Brachial-Basilar", "Syndromes, Brachial-Basilar Insufficiency", "stenosis of subclavian artery (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subclavian steal syndrome", "shortest_name_length": 22}
{"curie": "MONDO:0008601", "names": ["TRIGLYCERIDE STORAGE DISEASE, TYPE I", "Triglyceride Storage Disease, Type I", "triglyceride storage disease, type 1", "triglyceride storage disease, type I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "triglyceride storage disease, type 1", "shortest_name_length": 36}
{"curie": "MONDO:0013362", "names": ["BBIS", "BEAULIEU-BOYCOTT-INNES SYNDROME", "BEAULIEU-BOYCOTT-Innes syndrome", "Beaulieu Boycott Innes syndrome", "Beaulieu-Boycott-Innes syndrome", "BBIS - Beaulieu Boycott Innes syndrome", "THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome", "THO complex 6-related developmental delay, microcephaly, facial dysmorphism syndrome", "THO complex 6-related developmental delay, microcephaly, facial dysmorphism syndrome (disorder)", "THO complex 6-related developmental delay, microcephaly, facial dysmorphism syndrome (diagnosis)", "MICROCEPHALY, MENTAL RETARDATION, AND DISTINCTIVE FACIES, WITH CARDIAC AND GENITOURINARY MALFORMATIONS", "microcephaly, mental retardation, and distinctive facies, with Cardiac and genitourinary malformations", "microcephaly, intellectual disability, and distinctive facies, with Cardiac and genitourinary malformations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0016091", "names": ["adult Krabbe disease", "Krabbe disease of adults"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult Krabbe disease", "shortest_name_length": 20}
{"curie": "MONDO:0018946", "names": ["rhombencephalosynapsis", "Rhombencephalosynapsis", "Rhombencephalosynapsis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rhombencephalosynapsis", "shortest_name_length": 22}
{"curie": "MONDO:0019283", "names": ["nail anomaly", "nail epidermal appendage anomaly", "epidermal appendage anomaly of nail"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nail anomaly", "shortest_name_length": 12}
{"curie": "UMLS:C4759669", "names": ["Iodine deficiency", "iodine-deficiency", "iodine deficiency", "Iodine Deficiency", "deficiency iodine", "deficiency; iodine", "deficiencies iodine", "iodine deficiency disorder", "deficiency disorders iodine", "Iodine deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Iodine deficiency", "shortest_name_length": 17}
{"curie": "MONDO:0003649", "names": ["esophagus NET", "esophageal NEN", "esophageal NET", "Esophageal NET", "Esophageal NEN", "NEN of esophagus", "esophagus neuroendocrine tumor", "esophageal neuroendocrine tumor", "Esophageal Neuroendocrine Tumor", "esophageal neuroendocrine tumour", "neuroendocrine tumor of esophagus", "esophagus neuroendocrine neoplasm", "Esophageal Neuroendocrine Neoplasm", "esophageal neuroendocrine neoplasm", "Esophageal neuroendocrine neoplasm", "neuroendocrine tumour of oesophagus", "Neuroendocrine Neoplasm of Esophagus", "neuroendocrine neoplasm of esophagus", "Neuroendocrine neoplasm of esophagus", "Neuroendocrine Neoplasm of the Esophagus", "Esophageal Well Differentiated Endocrine Tumor", "esophageal well differentiated endocrine tumor", "esophageal well differentiated endocrine tumor/carcinoma", "Esophageal Well Differentiated Endocrine Tumor/Carcinoma", "esophagus neuroendocrine tumor, well differentiated, low or intermediate grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophageal neuroendocrine tumor", "shortest_name_length": 13}
{"curie": "UMLS:C2981676", "names": ["Stage IIA Pancreatic Cancer", "Stage IIA Pancreatic Cancer AJCC v6 and v7", "Stage IIA Exocrine and Endocrine Pancreatic Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Pancreatic Cancer AJCC v6 and v7", "shortest_name_length": 27}
{"curie": "MONDO:0021529", "names": ["Benign Chest Wall Tumor", "benign chest wall tumor", "chest wall benign neoplasm", "Benign Chest Wall Neoplasm", "benign tumor of chest wall", "Benign Tumor of Chest Wall", "benign chest wall neoplasm", "Benign Neoplasm of Chest Wall", "Benign neoplasm of chest wall", "benign neoplasm of chest wall", "Benign Tumor of the Chest Wall", "benign tumor of the chest wall", "benign neoplasm of the chest wall", "Benign Neoplasm of the Chest Wall", "Benign neoplasm of chest wall, NOS", "Benign neoplasm of chest wall (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of chest wall", "shortest_name_length": 23}
{"curie": "MONDO:0015301", "names": ["PCA", "PLCA", "Amyloid lichen", "amyloidosis IX", "skin amyloidosis", "Amyloidosis cutis", "amyloidosis cutis", "Lichen amyloidosus", "Lichen amyloidosis", "lichen amyloidosis", "amyloidosis lichen", "lichen amyloidosus", "Amyloidosis of skin", "amyloidosis of skin", "AD type amyloidosis", "cutaneous amyloidosis", "Cutaneous amyloidosis", "amyloidosis cutaneous", "CUTANEOUS AMYLOIDOSIS", "Amyloidosis of dermis", "lichen amyloidosis familial", "Primary cutaneous amyloidosis", "primary cutaneous amyloidosis", "Lichen amyloidosis (disorder)", "amyloidosis; lichen (etiology)", "lichen; amyloidosis (etiology)", "Amyloidosis of skin (disorder)", "Amyloidosis, Primary Cutaneous", "amyloidosis of skin (diagnosis)", "amyloidosis skin primary localized", "lichen; amyloidosis (manifestation)", "amyloidosis; lichen (manifestation)", "amyloidosis familial cutaneous lichen", "Primary Localized Cutaneous Amyloidosis", "primary localized cutaneous amyloidosis", "Primary localized cutaneous amyloidosis", "Primary localised cutaneous amyloidosis", "amyloidosis, primary localized cutaneous", "familial primary localized cutaneous amyloidosis", "Primary localized cutaneous amyloidosis (disorder)", "Primary localized cutaneous amyloidosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary cutaneous amyloidosis", "shortest_name_length": 3}
{"curie": "UMLS:C0751793", "names": ["Craniocervical Injury", "Craniocervical Injuries"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Craniocervical Injuries", "shortest_name_length": 21}
{"curie": "UMLS:C1519863", "names": ["Uterine Corpus Smooth Muscle Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Corpus Smooth Muscle Neoplasm", "shortest_name_length": 37}
{"curie": "UMLS:C5238474", "names": ["Advanced Bladder Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Bladder Carcinoma", "shortest_name_length": 26}
{"curie": "UMLS:C2987221", "names": ["Pancreatic Acinar Cell Cystadenoma", "Pancreatic Acinar Cystic Transformation", "Acinar Cystic Transformation of the Pancreas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acinar Cystic Transformation of the Pancreas", "shortest_name_length": 34}
{"curie": "UMLS:C3272410", "names": ["Gastric Large Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Large Cell Neuroendocrine Carcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0012688", "names": ["CATCN3", "CTRCT17", "cataract 17 multiple types", "CATARACT 17, MULTIPLE TYPES", "cataract 17, multiple types", "CRYBB1 early-onset non-syndromic cataract", "autosomal recessive congenital nuclear cataract 3", "cataract, congenital nuclear, autosomal recessive 3", "CATARACT, CONGENITAL NUCLEAR, AUTOSOMAL RECESSIVE 3", "Cataract, Congenital Nuclear, Autosomal Recessive 3", "CATARACT 17, MULTIPLE TYPES, WITH OR WITHOUT MICROCORNEA", "cataract 17, multiple types, with or without microcornea", "early-onset non-syndromic cataract caused by mutation in CRYBB1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 17 multiple types", "shortest_name_length": 6}
{"curie": "MONDO:0003654", "names": ["childhood parosteal osteosarcoma", "Childhood Parosteal Osteosarcoma", "Childhood Parosteal Osteogenic Sarcoma", "childhood parosteal osteogenic sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood parosteal osteosarcoma", "shortest_name_length": 32}
{"curie": "UMLS:C4054708", "names": ["Intermediate Chondrogenic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intermediate Chondrogenic Neoplasm", "shortest_name_length": 34}
{"curie": "UMLS:C1332894", "names": ["CNS T-Cell Lymphoma", "T-Cell Lymphoma of CNS", "T-Cell Lymphoma of the CNS", "Central Nervous System T-Cell Lymphoma", "T-Cell Lymphoma of Central Nervous System", "T-Cell Lymphoma of the Central Nervous System", "Central Nervous System T-Cell Non-Hodgkin Lymphoma", "Central Nervous System T-Cell Non-Hodgkin's Lymphoma", "Primary Central Nervous System T-Cell Non-Hodgkin's Lymphoma", "Central Nervous System T-Cell and NK-Cell Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System T-Cell Non-Hodgkin Lymphoma", "shortest_name_length": 19}
{"curie": "MONDO:0008080", "names": ["NF3", "Nf 3", "NF3A", "NF III", "neurofibromas, palmar cutaneous", "Neurofibromas, Palmar Cutaneous", "NEUROFIBROMAS, PALMAR CUTANEOUS", "Neurofibromatosis, Type III, of Riccardi", "NEUROFIBROMATOSIS, TYPE III, OF RICCARDI", "neurofibromatosis, type III, of Riccardi", "Neurofibromatosis, Type 3, Riccardi type", "neurofibromatosis, type III, Riccardi type", "Neurofibromatosis, Type III, Riccardi Type", "NEUROFIBROMATOSIS, TYPE III, RICCARDI TYPE", "Neurofibromatosis, Type 3, mixed central and peripheral", "Neurofibromatosis, Type III, Mixed Central and Peripheral", "neurofibromatosis, type III, mixed central and peripheral", "NEUROFIBROMATOSIS, TYPE III, MIXED CENTRAL AND PERIPHERAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurofibromatosis, type III, mixed central and peripheral", "shortest_name_length": 3}
{"curie": "MONDO:0007826", "names": ["Sinodonty", "SINODONTY", "Shovel-shaped incisor", "shovel-shaped incisors", "incisors, shovel-shaped", "INCISORS, SHOVEL-SHAPED", "Shovel-shaped incisor (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "incisors, shovel-shaped", "shortest_name_length": 9}
{"curie": "UMLS:C4324395", "names": ["Immune-mediated enterocolitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immune-mediated enterocolitis", "shortest_name_length": 29}
{"curie": "MONDO:0015018", "names": ["ARCI12", "ichthyosis, congenital, autosomal recessive 12", "ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 12", "ichthyosis, congenital, autosomal recessive type 12", "ichthyosis, congenital, autosomal recessive 12; ARCI12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ichthyosis, congenital, autosomal recessive 12", "shortest_name_length": 6}
{"curie": "MONDO:0007544", "names": ["EOS", "Eos", "Familial eosinophilia", "familial eosinophilia", "Eosinophilia, Familial", "EOSINOPHILIA, FAMILIAL", "eosinophilia, familial", "Hereditary eosinophilia", "hereditary eosinophilia", "Familial eosinophilia (disorder)", "Hereditary eosinophilia (disorder)", "hereditary eosinophilia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eosinophilia, familial", "shortest_name_length": 3}
{"curie": "MONDO:0010862", "names": ["T1D4", "IDDM4", "TYPE 1 DIABETES MELLITUS 4", "type 1 diabetes mellitus 4", "insulin-dependent diabetes mellitus 4", "Insulin-Dependent Diabetes Mellitus 4", "INSULIN-DEPENDENT DIABETES MELLITUS 4", "DIABETES MELLITUS, INSULIN-DEPENDENT, 4", "Diabetes Mellitus, Insulin-Dependent, 4", "diabetes mellitus, insulin-dependent, 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type 1 diabetes mellitus 4", "shortest_name_length": 4}
{"curie": "MONDO:0007373", "names": ["Band Keratopathy with Deafness", "band keratopathy with deafness", "BAND KERATOPATHY WITH DEAFNESS", "corneal degeneration, ribbonlike, with deafness", "Corneal Degeneration, Ribbonlike, with Deafness", "CORNEAL DEGENERATION, RIBBONLIKE, WITH DEAFNESS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal degeneration, ribbonlike, with deafness", "shortest_name_length": 30}
{"curie": "MONDO:0018669", "names": ["Snakebite", "snake bite", "Snake Bite", "Snakebites", "Bite, Snake", "Snake Bites", "snake bites", "Snake Envenoming", "Snake Envenomings", "Envenoming, Snake", "snake bite poison", "Snake envenomation", "snake envenomation", "Envenomings, Snake", "snake envenomations", "Snake bite poisoning", "snake bite poisoning", "snake venom poisoning", "Snake venom poisoning", "Snakebite envenomation", "snakebite envenomation", "bite; poisoning, snake", "Snakebite Envenomation", "Snakebite Envenomations", "Envenomation, Snakebite", "Snake bite poisoning, NOS", "Snake venom poisoning, NOS", "Adverse effect;venom;snake", "Toxic effect of snake venom", "poisoning by venomous snake", "Poisoning by venomous snake", "Snake venom causing toxic effect", "snake venom causing toxic effect", "Poisoning by venomous snake, NOS", "Poisoning caused by venomous snake", "poisoning caused by venomous snake", "Toxic effect of bite of venomous snake", "toxic effect of bite of venomous snake", "Toxic effect of bite of venomous snake, NOS", "Poisoning caused by venomous snake (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "snakebite envenomation", "shortest_name_length": 9}
{"curie": "MONDO:0002107", "names": ["Unilateral hyperactive labyrinth", "unilateral hyperactive labyrinth", "Hyperactive labyrinth, unilateral", "hyperactive labyrinth, unilateral", "unilateral hyperactive labyrinth (diagnosis)", "hyperactive unilateral labyrinthine dysfunction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "unilateral hyperactive labyrinth", "shortest_name_length": 32}
{"curie": "MONDO:0012376", "names": ["DFNB55", "autosomal recessive deafness 55", "DEAFNESS, AUTOSOMAL RECESSIVE 55", "Deafness, autosomal recessive 55", "deafness, autosomal recessive 55", "autosomal recessive nonsyndromic deafness 55", "autosomal recessive nonsyndromic hearing loss 55", "autosomal recessive nonsyndromic deafness type 55"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 55", "shortest_name_length": 6}
{"curie": "UMLS:C4054370", "names": ["Nephrotic Syndrome - PTPRO Associated", "Nephrotic Syndrome - GLEPP1 Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - PTPRO Associated", "shortest_name_length": 37}
{"curie": "MONDO:0100377", "names": ["AML, t(10;11)(p12;q23)", "acute myeloid leukemia, t(10;11)(p12;q23)", "Acute Myeloid Leukemia with t(10;11)(p12;q23); MLL-MLLT10", "Acute Myeloid Leukemia with t(10;11)(p12;q23); MLLT10-MLL", "Acute Myeloid Leukemia (AML) with t(10;11)(p12;q23); MLL-MLLT10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, t(10;11)(p12;q23)", "shortest_name_length": 22}
{"curie": "MONDO:0015759", "names": ["B-cell NHL", "B-cell lymphoma", "B-Cell Non-Hodgkin Lymphoma", "B-cell non-Hodgkin lymphoma", "B-cell non-Hodgkins lymphoma", "B-Cell Non-Hodgkin's Lymphoma", "B-cell non-Hodgkin's lymphoma", "non-Hodgkin's B-cell lymphoma", "Non-Hodgkin's B-Cell Lymphoma", "Non-Hodgkin's Lymphoma B-Cell", "B-Cell Non Hodgkin's Lymphoma", "non-Hodgkin's lymphoma B-cell", "B-cell non Hodgkin's lymphoma", "lymphomas non-Hodgkin's B-cell", "Lymphomas Non-Hodgkin's B-Cell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-cell non-Hodgkin lymphoma", "shortest_name_length": 10}
{"curie": "MONDO:0004124", "names": ["Prostate Stromal Sarcoma", "prostate stromal sarcoma", "stromal sarcoma of prostate", "Stromal Sarcoma of Prostate", "stromal sarcoma of the prostate", "Stromal Sarcoma of the Prostate", "Stromal sarcoma of the prostate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate stromal sarcoma", "shortest_name_length": 24}
{"curie": "MONDO:0005249", "names": ["pneum", "PNEUM", "Pneumonia", "PNEUMONIA", "pneumonia", "Pneumonias", "Pulmonitis", "Lung inflamed", "Pneumonia NOS", "Pneumonia, NOS", "acute pneumonia", "Pneumonitis, NOS", "lung inflammation", "Lung inflammation", "inflammation lungs", "Pneumonia (disorder)", "unspecified pneumonia", "pneumonia (diagnosis)", "Pneumonia, unspecified", "pulmonary inflammation", "Pulmonary inflammation", "Patient_developed_pneumonia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pneumonia", "shortest_name_length": 5}
{"curie": "MONDO:0004860", "names": ["vitreous disease", "vitreous disorder", "vitreous humor disease", "Other vitreous opacities", "disease of vitreous humor", "disorder of vitreous humor", "vitreous humor disease or disorder", "disease or disorder of vitreous humor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitreous disorder", "shortest_name_length": 16}
{"curie": "UMLS:C3272419", "names": ["Benign Gastric Gastrointestinal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Gastric Gastrointestinal Stromal Tumor", "shortest_name_length": 45}
{"curie": "UMLS:C0405169", "names": ["Secondary uterine inertia", "secondary uterine inertia", "Uterine inertia, secondary", "uterus; inertia, secondary", "Secondary uterine inertia (disorder)", "secondary uterine inertia (diagnosis)", "Secondary hypotonic uterine dysfunction", "secondary hypotonic uterine dysfunction", "Hypotonic uterine dysfunction, secondary", "inertia; uterus, during labor, secondary", "secondary hypotonic uterine dysfunction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary uterine inertia", "shortest_name_length": 25}
{"curie": "UMLS:C4053936", "names": ["Thyroglobulin Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroglobulin Deficiency", "shortest_name_length": 24}
{"curie": "UMLS:C1333829", "names": ["Grade 1 Clear Cell Renal Cell Carcinoma", "Grade 1 Conventional (Clear Cell) Renal Cell Carcinoma", "G1 Nuclei round, uniform, approximately 10 um; nucleoli inconspicuous or absent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade 1 Clear Cell Renal Cell Carcinoma", "shortest_name_length": 39}
{"curie": "MONDO:0011038", "names": ["CAPOS", "CAPOS syndrome", "CAPOS SYNDROME", "Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural deafness syndrome", "cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss", "Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss", "Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorineural hearing loss", "CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURAL HEARING LOSS", "cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss", "Cerebellar Ataxia, Areflexia, Pes Cavus, Optic Atrophy, And Sensorineural Hearing Loss", "cerebellar ataxia - areflexia - pes cavus - optic atrophy - sensorineural hearing loss", "cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome", "Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome", "Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome", "CAPOS (cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss) syndrome", "Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0025363", "names": ["Psychosocial Mental Retardation", "Psychosocial Mental Retardations", "Retardation, Psychosocial Mental", "Mental Retardation, Psychosocial", "Mental Retardations, Psychosocial", "Retardations, Psychosocial Mental", "Cultural Familial Mental Retardation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mental Retardation, Psychosocial", "shortest_name_length": 31}
{"curie": "MONDO:0002098", "names": ["Facial Myokymia", "Facial myokymia", "facial myokymia", "Facial Myokymias", "facial myokymias", "Myokymia, Facial", "myokymia; facial", "facial neuropathy", "Facial Neuropathy", "Myokymias, Facial", "Facial neuropathy", "Neuropathy, Facial", "Facial Neuropathies", "Neuropathies, Facial", "Facial Nerve Disease", "facial nerve palsies", "facial nerve disease", "facial nerve diseases", "disorder facial nerve", "Facial Nerve Disorder", "facial nerve disorder", "Disease, Facial Nerve", "Facial Nerve Diseases", "Facial nerve disorder", "Facial nerve--Diseases", "facial nerve disorders", "Facial Nerve Disorders", "Facial nerve disorders", "Disorder, Facial Nerve", "Diseases, Facial Nerve", "disease of facial nerve", "Disorders, Facial Nerve", "facial myokymia was seen", "disorder of facial nerve", "Disorder of facial nerve", "Facial myokymia (finding)", "Facial nerve disorder NOS", "cranial nerve vii diseases", "Cranial Nerve VII Diseases", "Facial nerve disorder, NOS", "Disorder of cranial nerve 7", "facial myokymia (diagnosis)", "Cranial Nerve VII Disorders", "Involuntary facial quivering", "disorders of the seventh nerve", "Involuntary facial contraction", "Seventh Cranial Nerve Diseases", "Seventh cranial nerve disorder", "Facial cranial nerve disorders", "Disorders of the seventh nerve", "Facial nerve disease or syndrome", "facial nerve disease or disorder", "Facial nerve disorder (disorder)", "Disorder of seventh cranial nerve", "disorder of seventh cranial nerve", "Facial nerve disorder, unspecified", "facial myokymia (physical finding)", "Facial myokymia (muscle quivering)", "disease (or disorder); facial nerve", "disease or disorder of facial nerve", "disorder of facial nerve (diagnosis)", "Disorders of the VIIth cranial nerve", "disorders of the VIIth cranial nerve", "Disorder of facial nerve, unspecified", "Disorder of seventh cranial nerve, NOS", "Seventh cranial nerve disease or syndrome", "disease (or disorder); cranial nerve, seventh"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "facial nerve disorder", "shortest_name_length": 15}
{"curie": "MONDO:0018435", "names": ["AML with inv3(p21;q26.2) or t(3;3)(p21;q26.2)", "AML with inv3(q21;q26.2) or t(3;3)(q21;q26.2)", "acute myeloid leukemia with inv3(p21;q26.2) or t(3;3)(p21;q26.2)", "acute myeloid leukemia with inv3(q21;q26.2) or t(3;3)(q21;q26.2)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia with inv3(p21;q26.2) or t(3;3)(p21;q26.2)", "shortest_name_length": 45}
{"curie": "MONDO:0010932", "names": ["Crapb", "CRAPB", "PBCRA", "PROGRESSIVE BIFOCAL CHORIORETINAL ATROPHY", "progressive bifocal chorioretinal atrophy", "Progressive bifocal chorioretinal atrophy", "CHORIORETINAL ATROPHY, PROGRESSIVE BIFOCAL", "chorioretinal atrophy, progressive bifocal", "Chorioretinal atrophy, progressive bifocal", "CRAPB Chorioretinal atrophy progressive bifocal", "PBCRA Progressive bifocal chorioretinal atrophy", "Progressive bifocal chorioretinal atrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive bifocal chorioretinal atrophy", "shortest_name_length": 5}
{"curie": "MONDO:0003200", "names": ["UAD", "urethra adenocarcinoma", "Urethra Adenocarcinoma", "Urethral Adenocarcinoma", "urethral adenocarcinoma", "Adenocarcinoma of Urethra", "adenocarcinoma of urethra", "adenocarcinoma of the urethra", "Adenocarcinoma of the Urethra", "adenocarcinoma of urethra (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urethra adenocarcinoma", "shortest_name_length": 3}
{"curie": "UMLS:C0854961", "names": ["stage II vulvar cancer", "Stage II Vulvar Cancer", "FIGO Stage II Vulva Carcinoma", "Vulva Cancer Stage II AJCC v6", "AJCC Stage II Vulva Cancer v6", "Stage II Vulva Cancer AJCC v6", "Stage II Vulvar Cancer AJCC v6", "Vulval Cancer Stage II AJCC v6", "FIGO Stage II Vulvar Carcinoma", "FIGO Stage II Carcinoma of Vulva", "FIGO Stage II Carcinoma of the Vulva"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Vulva Cancer AJCC v6", "shortest_name_length": 22}
{"curie": "MONDO:0003821", "names": ["ovarian biphasic or triphasic teratoma", "Ovarian Biphasic or Triphasic Teratoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian biphasic or triphasic teratoma", "shortest_name_length": 38}
{"curie": "OMIM:611742", "names": ["SHEP9", "Shep9", "SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 9", "Skin-Hair-Eye Pigmentation, Variation In, 9", "Skin-Hair-Eye Pigmentation 9, Red-Nonred Hair", "SKIN/HAIR/EYE PIGMENTATION 9, DARK/LIGHT HAIR", "SKIN/HAIR/EYE PIGMENTATION 9, RED/NONRED HAIR", "Skin-Hair-Eye Pigmentation 9, Dark-Light Hair", "SKIN/HAIR/EYE PIGMENTATION 9, FRECKLING/SUNBURN", "Skin-Hair-Eye Pigmentation 9, Brown-Nonbrown Eyes", "SKIN/HAIR/EYE PIGMENTATION 9, BROWN/NONBROWN EYES", "Skin-Hair-Eye Pigmentation 9, Freckling And Burning", "SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 9 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 5}
{"curie": "MONDO:0800139", "names": ["HELIOS deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HELIOS deficiency", "shortest_name_length": 17}
{"curie": "UMLS:C4525093", "names": ["Stage IIIC Colorectal Cancer AJCC v8", "Stage IIIC Colorectal Carcinoma AJCC v8", "Stage IIIC Colorectal (Colon or Rectal) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Colorectal Cancer AJCC v8", "shortest_name_length": 36}
{"curie": "MONDO:0008500", "names": ["STRIAE DISTENSAE, FAMILIAL", "striae distensae, familial", "Striae Distensae, Familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "striae distensae, familial", "shortest_name_length": 26}
{"curie": "MONDO:0100285", "names": ["EHBA", "Extrahepatic Biliary Atresia", "extrahepatic biliary atresia", "Extrahepatic biliary atresia", "Biliary atresia, extrahepatic", "Biliary Atresia, Extrahepatic", "biliary atresia, extrahepatic", "BILIARY ATRESIA, EXTRAHEPATIC", "Atresia, Extrahepatic Biliary", "Extrahepatic bile duct atresia", "Extrahepatic biliary duct atresia", "EHBA - Extrahepatic biliary atresia", "Congenital Extrahepatic Biliary Atresia", "Congenital atresia of extrahepatic bile duct", "Congenital atresia of extrahepatic bile duct (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extrahepatic biliary atresia", "shortest_name_length": 4}
{"curie": "UMLS:C0162699", "names": ["Tick-Borne Infection", "Tick Borne Infection", "Tick-Borne Infections", "Infection, Tick-Borne", "Tick Borne Infections", "Infections, Tick Borne", "Infections, Tick-Borne"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tick-Borne Infections", "shortest_name_length": 20}
{"curie": "UMLS:C0040441", "names": ["Crack", "chip tooth", "Broken tooth", "broken tooth", "teeth broken", "Broken teeth", "broken teeth", "teeth; broken", "broken; tooth", "tooth chipped", "Chipped tooth", "chipped tooth", "tooth fracture", "Tooth fracture", "Tooth Fracture", "fracture tooth", "Tooth Fractures", "Fractured tooth", "fracture; tooth", "Fractured teeth", "tooth; fracture", "Fracture, Tooth", "tooth fractures", "fractured tooth", "tooth fractured", "Fractures, Tooth", "BT - Broken tooth", "Fracture of teeth", "Fracture of tooth", "fracture of tooth", "BT - broken tooth", "Fracture of Tooth", "Fracture;tooth/teeth", "chipped tooth (symptom)", "fracture of tooth or teeth", "Fracture of teeth (disorder)", "Fracture of tooth (disorder)", "fracture of tooth (diagnosis)", "tooth fracture (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tooth Fractures", "shortest_name_length": 5}
{"curie": "UMLS:C3160756", "names": ["Infection reactivation", "Reactivation Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reactivation Infection", "shortest_name_length": 22}
{"curie": "MONDO:0010299", "names": ["HRH", "HPRT-related gout", "Gout, HPRT-Related", "GOUT, HPRT-RELATED", "gout, HPRT-related", "HPRT partial deficiency", "HPRT Deficiency, Partial", "HPRT deficiency, grade I", "HPRT deficiency, partial", "HPRT DEFICIENCY, PARTIAL", "HPRT1 partial deficiency", "Partial HGPRT deficiency", "HPRT1 Deficiency, Partial", "HPRT1 DEFICIENCY, PARTIAL", "Hprt1 deficiency, partial", "Kelley-Seegmiller Syndrome", "KELLEY-SEEGMILLER SYNDROME", "HPRT-related hyperuricemia", "Kelley-Seegmiller syndrome", "KELLEY-Seegmiller syndrome", "HRPT-related hyperuricemia", "HYPERURICEMIA, HPRT-RELATED", "hyperuricemia, HRPT-related, X-linked recessive", "Hypoxanthine guanine phosphoribosyltransferase partial deficiency", "Partial hypoxanthine-guanine phosphoribosyltransferase deficiency", "hypoxanthine guanine phosphoribosyltransferase partial deficiency", "hypoxanthine guanine phosphoribosyltransferase deficiency, grade I", "Partial hypoxanthine-guanine phosphoribosyl transferase deficiency", "Hypoxanthine guanine phosphoribosyltransferase deficiency, grade I", "Hypoxanthine guanine phosphoribosyltransferase 1 partial deficiency", "hypoxanthine guanine phosphoribosyltransferase 1 partial deficiency", "hypoxanthine guanine phosphoribosyltransferase 1 deficiency, partial", "HYPOXANTHINE GUANINE PHOSPHORIBOSYLTRANSFERASE 1 DEFICIENCY, PARTIAL", "Hypoxanthine Guanine Phosphoribosyltransferase 1 Deficiency, Partial", "Partial hypoxanthine-guanine phosphoribosyltransferase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypoxanthine guanine phosphoribosyltransferase partial deficiency", "shortest_name_length": 3}
{"curie": "UMLS:C0269190", "names": ["cervix squamous metaplasia", "squamous metaplasia cervix", "cervix metaplasia squamous", "CERVICAL METAPLASIA SQUAMOUS", "Cervical Metaplasia Squamous", "Cervical Squamous Metaplasia", "cervical squamous metaplasia", "Squamous Metaplasia of Cervix", "Squamous metaplasia of cervix", "squamous metaplasia of cervix", "Uterine cervical squamous metaplasia", "Squamous metaplasia of cervix (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Squamous metaplasia of cervix", "shortest_name_length": 26}
{"curie": "UMLS:C1334774", "names": ["Minor Salivary Gland Epidermoid Carcinoma", "Minor Salivary Gland Squamous Cell Carcinoma", "Epidermoid Carcinoma of Minor Salivary Gland", "Squamous Cell Carcinoma of Minor Salivary Gland", "Epidermoid Carcinoma of the Minor Salivary Gland", "Squamous Cell Carcinoma of the Minor Salivary Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Minor Salivary Gland Squamous Cell Carcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0018326", "names": ["NMG", "Neonatal myasthenia gravis", "neonatal myasthenia gravis", "Transient neonatal myasthenia", "Transient neonatal myasthenia gravis", "Transient Neonatal Myasthenia Gravis", "myasthenia gravis neonatal transient", "transient neonatal myasthenia gravis", "Neonatal Myasthenia Gravis, Transient", "Myasthenia Gravis, Transient, Neonatal", "Transient neonatal acquired myasthenia", "Myasthenia Gravis, Neonatal, Transient", "transient neonatal acquired myasthenia", "myasthenia; gravis, neonatal, transient", "transient neonatal autoimmune myasthenia gravis", "Transient neonatal autoimmune myasthenia gravis", "Transient neonatal myasthenia gravis (disorder)", "Transient neonatal myasthenia gravis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transient neonatal myasthenia gravis", "shortest_name_length": 3}
{"curie": "UMLS:C3272805", "names": ["Colorectal Adenomatous Polyp", "Large Bowel Adenomatous Polyp", "Adenomatous Polyp of Large Bowel", "Adenomatous Polyp of the Large Bowel"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Adenomatous Polyp", "shortest_name_length": 28}
{"curie": "UMLS:C0496871", "names": ["Benign Extrahepatic Bile Duct Tumor", "Benign Tumor of Extrahepatic Bile Duct", "Benign Extrahepatic Bile Duct Neoplasm", "Benign tumor of extrahepatic bile duct", "benign tumor of extrahepatic bile duct", "Benign tumour of extrahepatic bile duct", "benign neoplasm of extrahepatic bile duct", "Benign Neoplasm of Extrahepatic Bile Duct", "Benign Tumor of the Extrahepatic Bile Duct", "Benign neoplasm of extrahepatic bile ducts", "Benign Neoplasm of the Extrahepatic Bile Duct", "Benign neoplasm of extrahepatic bile ducts, NOS", "benign neoplasm of extrahepatic bile duct (diagnosis)", "Benign neoplasm of extrahepatic bile ducts (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign neoplasm of extrahepatic bile ducts", "shortest_name_length": 35}
{"curie": "MONDO:0010950", "names": ["T1D8", "IDDM8", "TYPE 1 DIABETES MELLITUS 8", "type 1 diabetes mellitus 8", "INSULIN-DEPENDENT DIABETES MELLITUS 8", "insulin-dependent diabetes mellitus 8", "Insulin-Dependent Diabetes Mellitus 8", "Diabetes Mellitus, Insulin-Dependent, 8", "diabetes mellitus, insulin-dependent, 8", "DIABETES MELLITUS, INSULIN-DEPENDENT, 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type 1 diabetes mellitus 8", "shortest_name_length": 4}
{"curie": "UMLS:C0158337", "names": ["synovium rupture", "Synovial rupture", "ruptured synovium", "synovium; rupture", "rupture; synovium", "Rupture of synovium", "rupture of synovium", "Rupture of synovium, NOS", "ruptured synovium (diagnosis)", "Rupture of synovium (disorder)", "Rupture of synovium, unspecified", "Rupture of synovium, site unspecified", "Rupture of synovium, unspecified joint"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rupture of synovium", "shortest_name_length": 16}
{"curie": "MONDO:0024512", "names": ["SPDA", "spondyloarthropathy, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloarthropathy, susceptibility to", "shortest_name_length": 4}
{"curie": "MONDO:0006595", "names": ["perinatal jaundice from hepatocellular damage", "perinatal jaundice due to hepatocellular damage", "Perinatal jaundice due to hepatocellular damage", "perinatal jaundice from hepatocellular damage (diagnosis)", "Perinatal jaundice due to hepatocellular damage (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "perinatal jaundice due to hepatocellular damage", "shortest_name_length": 45}
{"curie": "UMLS:C4725865", "names": ["Resectable Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Carcinoma", "shortest_name_length": 20}
{"curie": "MONDO:0002330", "names": ["alcohol psychosis", "Alcoholic Psychosis", "Alcoholic Psychoses", "ALCOHOLIC PSYCHOSIS", "alcoholic psychoses", "Psychosis;alcoholic", "Psychosis alcoholic", "Alcoholic psychosis", "Alcoholic psychoses", "alcoholic psychosis", "psychosis; alcoholic", "Psychoses, Alcoholic", "alcoholism; psychosis", "Alcoholic psychosis NOS", "Alcoholic psychosis, NOS", "Alcohol-induced psychosis", "Alcoholism with psychosis", "alcohol induced psychosis", "Ethanol-induced psychosis", "Psychosis caused by ethanol", "Alcohol-induced psychosis, NOS", "Alcoholic neurologic psychosis", "Unspecified alcoholic psychosis", "Alcoholic psychosis, unspecified", "Alcohol-induced psychotic disorder", "alcohol-induced psychotic disorder", "Psychosis caused by ethanol (disorder)", "Unspecified alcohol-induced mental disorders", "alcohol-induced psychotic disorder (diagnosis)", "disorder; psychotic, alcohol (due to), alcoholic", "psychotic; disorder, alcohol (due to), alcoholic", "Mental and behavioral disorders due to use of alcohol, psychotic disorder", "Mental and behavioural disorders due to use of alcohol, psychotic disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alcoholic psychosis", "shortest_name_length": 17}
{"curie": "MONDO:0021138", "names": ["bone marrow cancer", "Bone marrow--Cancer", "cancer of bone marrow", "Neoplasm malig;bone;marrow", "Malignant Bone Marrow Tumor", "malignant bone marrow tumor", "malignant tumor of bone marrow", "malignant bone marrow neoplasm", "Malignant Bone Marrow Neoplasm", "malignant neoplasm of bone marrow", "malignant neosplasm of the bonemarrow", "Malignant neoplasm of bone marrow NOS", "malignant neoplasm of bone marrow (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bone marrow cancer", "shortest_name_length": 18}
{"curie": "MONDO:0009851", "names": ["Peripheral Neuropathy, Ataxia, Focal Necrotizing Encephalopathy, and Spongy Degeneration of Brain", "peripheral neuropathy, ataxia, focal necrotizing encephalopathy, and spongy degeneration of brain", "PERIPHERAL NEUROPATHY, ATAXIA, FOCAL NECROTIZING ENCEPHALOPATHY, AND SPONGY DEGENERATION OF BRAIN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peripheral neuropathy, ataxia, focal necrotizing encephalopathy, and spongy degeneration of brain", "shortest_name_length": 97}
{"curie": "UMLS:C0852694", "names": ["cartilage injury", "Cartilage damage", "Cartilage injury", "Cartilage Injury", "cartilage injuries", "Injury of cartilage", "Injury of cartilage (disorder)", "Injury of cartilage (diagnosis)", "disorders of connective tissue injury of cartilage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cartilage injury", "shortest_name_length": 16}
{"curie": "MONDO:0013919", "names": ["EIG12", "idiopathic generalized epilepsy 12", "susceptibility to idiopathic generalized epilepsy 12", "EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 12", "epilepsy, idiopathic generalized, susceptibility to, 12", "epilepsy, idiopathic generalized, susceptibility to, type 12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, idiopathic generalized, susceptibility to, 12", "shortest_name_length": 5}
{"curie": "UMLS:C5575342", "names": ["Astrocytoma, NOS", "Astrocytoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Astrocytoma, Not Otherwise Specified", "shortest_name_length": 16}
{"curie": "MONDO:0004558", "names": ["Colloid Adenoma", "colloid adenoma", "Colloid adenoma", "macrofollicular adenoma", "Macrofollicular Adenoma", "Macrofollicular adenoma", "colloid; adenoma, unspecified site", "thyroid gland macrofollicular adenoma", "Thyroid Gland Macrofollicular Adenoma", "Macrofollicular adenoma (morphologic abnormality)", "macrofollicular adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid gland macrofollicular adenoma", "shortest_name_length": 15}
{"curie": "MONDO:0030891", "names": ["MRD66", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 66", "mental retardation, autosomal dominant 66", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 66", "intellectual developmental disorder, autosomal dominant 66"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder, autosomal dominant 66", "shortest_name_length": 5}
{"curie": "MONDO:0017685", "names": ["vitamin B12-responsive methylmalonic aciduria, type cblDv2", "vitamin B12-responsive methylmalonic acidemia, type cblDv2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitamin B12-responsive methylmalonic acidemia, type cblDv2", "shortest_name_length": 58}
{"curie": "UMLS:C0434028", "names": ["Gallbladder injury", "Gallbladder Injury", "gallbladder; injury", "injury; gallbladder", "injury of gallbladder", "Injury of gallbladder", "Injury of gallbladder (disorder)", "injury of gallbladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of gallbladder", "shortest_name_length": 18}
{"curie": "UMLS:C1707401", "names": ["Classical Poroma", "Classical Eccrine Poroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Classical Poroma", "shortest_name_length": 16}
{"curie": "MONDO:0004279", "names": ["Glossopharyngeal Motor Neuropathy", "glossopharyngeal motor neuropathy", "Motor Neuropathy, Glossopharyngeal", "Glossopharyngeal Motor Neuropathies", "Motor Neuropathies, Glossopharyngeal", "glossopharyngeal nerve motor peripheral neuropathy", "motor peripheral neuropathy of glossopharyngeal nerve"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glossopharyngeal motor neuropathy", "shortest_name_length": 33}
{"curie": "MONDO:0007946", "names": ["jaw wink", "jaw winking", "JAW-WINKING", "winking jaw", "jaw-winking", "Marcus Gunn", "Jaw-winking", "Jaw winking", "Jaw-blinking", "Jaw blinking", "jaw-blinking", "Marcus Gunn syndrome", "Jaw-winking syndrome", "jaw winking syndrome", "Jaw winking syndrome", "marcus gunn syndrome", "Marcus-Gunn syndrome", "jaw-winking syndrome", "syndrome; jaw-winking", "jaw-winking; syndrome", "Marcus Gunn's syndrome", "Marcus Gunn phenonemon", "Marcus Gunn phenomenon", "MARCUS GUNN PHENOMENON", "Marcus-Gunn phenomenon", "Marcus-Gunn jaw winking", "Marcus Gunn jaw winking", "maxillopalpebral synkinesis", "MAXILLOPALPEBRAL SYNKINESIS", "Maxillopalpebral synkinesis", "Pterygoid-levator synkinesis", "pterygoid-levator synkinesis", "Marcus-Gunn jaw-wink syndrome", "Jaw-winking syndrome (disorder)", "Trigemino-oculomotor synkinesis", "familial Marcus Gunn phenomenon", "Marcus-Gunn syndrome (diagnosis)", "Marcus Gunn jaw-winking syndrome", "Marcus Gunn jaw winking synkinesis", "Abnormal eyelid innervation syndrome", "Abnormal innervation syndrome of eyelid", "abnormal innervation syndrome of eyelid", "familial Marcus Gunn phenomenon (subtype)", "Mandibulo-palpebral synkinesis-ptosis syndrome", "mandibulo-palpebral synkinesis-ptosis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "jaw-winking syndrome", "shortest_name_length": 8}
{"curie": "MONDO:0001358", "names": ["BRONCHOSPASM", "bronchospasm", "Bronchospasm", "Bronchospasms", "bronchospasms", "Spasm bronchial", "SPASM BRONCHIAL", "Bronchial spasm", "bronchus; spasm", "Bronchial Spasm", "bronchial spasm", "Bronchial Spasms", "bronchus disease", "spasm; bronchial", "Spasm, Bronchial", "Bronchospasm NOS", "bronchial spasms", "Bronchial Disease", "Bronchi--Diseases", "Bronchial disease", "bronchial disease", "Spasms, Bronchial", "bronchus disorder", "bronchus; disorder", "bronchial disorder", "Bronchial disorder", "bronchial diseases", "Disease, Bronchial", "Bronchial Diseases", "Diseases, Bronchial", "Bronchial Disorders", "disease of bronchus", "bronchial disorders", "Disorder of bronchus", "disorder of bronchus", "Bronchospasm (finding)", "constriction; bronchus", "bronchus; constriction", "DISEASES OF THE BRONCHI", "Disease of bronchus, NOS", "bronchospasm (diagnosis)", "bronchus disease or disorder", "disease or disorder of bronchus", "disease (or disorder); bronchus", "Disorder of bronchus (disorder)", "disease of bronchus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bronchial disorder", "shortest_name_length": 12}
{"curie": "MONDO:0015249", "names": ["Mitral atresia", "mitral atresia", "mitral; atresia", "atresia; mitral", "MA - Mitral atresia", "Mitral valve atresia", "Mitral Valve Atresia", "mitral valve atresia", "mitral atresia disorder", "mitral atresia (diagnosis)", "congenital mitral valve atresia", "Congenital Mitral Valve Atresia", "congenital atresia of mitral valve", "Congenital atresia of mitral valve", "Congenital Atresia of Mitral Valve", "Congenital atresia of mitral valve (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitral atresia disorder", "shortest_name_length": 14}
{"curie": "MONDO:0004503", "names": ["upper clivus meningioma", "Upper Clivus Meningioma", "meningioma of upper clivus", "Meningioma of Upper Clivus", "Meningioma of the Upper Clivus", "meningioma of the upper clivus", "meningioma of the Upper Clivus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "upper clivus meningioma", "shortest_name_length": 23}
{"curie": "MONDO:0007016", "names": ["HYPOVITAMINOSIS A", "Hypovitaminosis A", "deficiency vitamins", "Vitamin A Deficiency", "vitamin a deficiency", "Vitamin A deficiency", "deficiency vitamin a", "vitamin A deficiency", "VITAMIN A DEFICIENCY", "deficiencies vitamin", "deficiencies vitamins", "Hypovitaminosis A NOS", "deficiency, vitamin A", "Deficiency, Vitamin A", "Hypovitaminosis A, NOS", "Vitamin A Deficiencies", "vitamin A deficiencies", "deficiency; vitamin, A", "vitamin; deficiency, A", "vitamin a deficiencies", "deficiencies, vitamin A", "of vitamin a deficiency", "deficiency of vitamin a", "Deficiency of vitamin A", "Deficiencies, Vitamin A", "Low levels of vitamin A", "Vitamin A deficiency, NOS", "vitamin deficiency disease", "deficiency diseases vitamin", "Vitamin A deficiency disease", "vitamin a deficiency disorder", "deficiencies disease vitamins", "vitamin A deficiency (disease)", "Vitamin A deficiency (disorder)", "Unspecified vitamin A deficiency", "vitamin a deficiency (diagnosis)", "Vitamin A deficiency, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitamin A deficiency", "shortest_name_length": 17}
{"curie": "UMLS:C5555883", "names": ["Metaplastic Papillary Lesion", "Fallopian Tube Metaplastic Papillary Lesion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fallopian Tube Metaplastic Papillary Lesion", "shortest_name_length": 28}
{"curie": "MONDO:0034556", "names": ["vibratory angioedema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vibratory angioedema", "shortest_name_length": 20}
{"curie": "MONDO:0043127", "names": ["mehta lewis patton syndrome", "Mehta Lewis Patton syndrome", "Congenital heart disease, ptosis, hypodontia, and craniosynostosis", "congenital heart disease, ptosis, hypodontia, and craniosynostosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mehta lewis patton syndrome", "shortest_name_length": 27}
{"curie": "MONDO:0000345", "names": ["Oropouche Fever", "Oropouche fever", "fever; Oropouche", "Oropouche Fevers", "Oropouche; fever", "Oropouche Infection", "Oropouche virus disease", "Oropouche Virus Infection", "Virus Infection, Oropouche", "Oropouche fever (diagnosis)", "Oropouche virus infectious disease", "Oropouche virus disease (disorder)", "Oropouche Orthobunyavirus Infection", "Oropouche virus disease or disorder", "Orthobunyavirus Infection, Oropouche", "Mosquito-borne viral fever, Oropouche", "Oropouche virus caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oropouche fever", "shortest_name_length": 15}
{"curie": "UMLS:C2981678", "names": ["stage IIIA penile cancer", "Stage IIIa Penile Cancer", "Stage IIIA Penile Cancer", "Stage IIIa Penile Cancer AJCC v7", "stage IIIA penile cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIa Penile Cancer AJCC v7", "shortest_name_length": 24}
{"curie": "UMLS:C0877339", "names": ["Cardio-respiratory distress"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardio-respiratory distress", "shortest_name_length": 27}
{"curie": "MONDO:0019365", "names": ["Scrub Typhus", "Kedani fever", "scrub typhus", "Scrub typhus", "TYPHUS, SCRUB", "scrub; typhus", "kedani; fever", "tsutsugamushi", "fever; kedani", "scrubs typhus", "typhus; scrub", "Typhus, Scrub", "Tsutsugamushi", "typhus; kedani", "kedani; typhus", "Tropical typhus", "tropical typhus", "Japanese; typhus", "typhus; tropical", "tropical; typhus", "typhus; Japanese", "TYPHUS, TROPICAL", "Mite-borne typhus", "mite-borne; typhus", "typhus; mite-borne", "Tsutsugamushi Fever", "tsutsugamushi fever", "Tsutsugamushi fever", "fever; Sumatran mite", "fever; tsutsugamushi", "Sumatran mite; fever", "Chigger-borne typhus", "Tsutsugamushi Fevers", "tsutsugamushi; fever", "Japanese river fever", "chigger-borne typhus", "Fever, Tsutsugamushi", "tsutsugamushi disease", "Tsutsugamushi Disease", "Fevers, Tsutsugamushi", "Sumatran mite; typhus", "Japanese river; fever", "typhus; Sumatran mite", "fever; Japanese river", "TSUTSUGAMUSHI DISEASE", "FEVER, JAPANESE RIVER", "Tsutsugamushi disease", "Disease, Tsutsugamushi", "Tsutsugamushi Diseases", "Diseases, Tsutsugamushi", "scrub mite-borne typhus", "Scrub mite-borne typhus", "Scrub typhus (disorder)", "Mite-borne rickettsiosis", "scrub (mite-borne) typhus", "Scrub (mite-borne) typhus", "Chigger-borne rickettsiosis", "chigger-borne rickettsiosis", "typhus; Rickettsia tsutsugamushi", "Orientia tsutsugamushi Infection", "Orientia tsutsugamushi Infections", "Infection, Orientia tsutsugamushi", "Rickettsia; tsutsugamushi, typhus", "Infections, Orientia tsutsugamushi", "Rickettsia tsutsugamushi infection", "scrub typhus (Tsutsugamushi disease)", "rickettsiosis; Rickettsia tsutsugamushi", "typhus fever due to Rickettsia tsutsugamushi", "Typhus fever due to Rickettsia tsutsugamushi", "tsutsugamushi; Rickettsia tsutsugamushi, typhus", "scrub typhus (Tsutsugamushi disease) (diagnosis)", "Mite-borne typhus due to Rickettsia tsutsugamushi", "Typhus fever due to Orientia Tsutsugamushi (scrub typhus)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scrub typhus", "shortest_name_length": 12}
{"curie": "UMLS:C1335373", "names": ["Penile Non-Neoplastic Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Penile Non-Neoplastic Disorder", "shortest_name_length": 30}
{"curie": "UMLS:C5555539", "names": ["Recurrent Anaplastic (Malignant) Meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Anaplastic (Malignant) Meningioma", "shortest_name_length": 43}
{"curie": "MONDO:0040677", "names": ["invasive carcinoma", "Invasive Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "invasive carcinoma", "shortest_name_length": 18}
{"curie": "UMLS:C3896960", "names": ["Pre-B Acute Lymphoblastic Leukemia", "Childhood Pre-B Acute Lymphoblastic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Pre-B Acute Lymphoblastic Leukemia", "shortest_name_length": 34}
{"curie": "MONDO:0010398", "names": ["MRXS14", "MENTAL RETARDATION, X-LINKED, SYNDROMIC 14", "Mental Retardation, X-Linked, Syndromic 14", "mental retardation, X-linked, syndromic 14", "syndromic X-linked intellectual disability 14", "intellectual disability, X-linked, syndromic 14", "mental retardation, X-linked, syndromic type 14", "UPF3B X-linked syndromic intellectual disability", "syndromic X-linked intellectual disability type 14", "intellectual disability, X-linked, syndromic type 14", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 14", "X-linked syndromic intellectual disability caused by mutation in UPF3B", "intellectual developmental disorder, X-linked syndromic 14, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic X-linked intellectual disability 14", "shortest_name_length": 6}
{"curie": "MONDO:0024306", "names": ["lactic acidosis", "acquired lactic acidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired lactic acidosis", "shortest_name_length": 15}
{"curie": "MONDO:0014106", "names": ["HH20", "FGF17 hypogonadotropic hypogonadism", "HYPOGONADOTROPIC HYPOGONADISM 20 WITH OR WITHOUT ANOSMIA", "hypogonadotropic hypogonadism 20 with or without anosmia", "hypogonadotropic hypogonadism caused by mutation in FGF17"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadotropic hypogonadism 20 with or without anosmia", "shortest_name_length": 4}
{"curie": "UMLS:C4054404", "names": ["Nephropathy due to Ciclosporin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephropathy due to Ciclosporin", "shortest_name_length": 30}
{"curie": "MONDO:0013797", "names": ["Del(17)(q12)", "Monosomy 17q12", "monosomy 17q12", "17q12 deletion syndrome", "17q12 microdeletion syndrome", "17q12 recurrent deletion syndrome", "chromosome 17q12 deletion syndrome", "CHROMOSOME 17q12 DELETION SYNDROME", "17q12 microdeletion syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 17q12 deletion syndrome", "shortest_name_length": 12}
{"curie": "UMLS:C3840002", "names": ["Non-small cell lung cancer with mutation in epidermal growth factor receptor", "Non-small cell lung cancer with mutation in epidermal growth factor receptor (disorder)", "Non-small cell lung cancer with mutation in epidermal growth factor receptor (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-small cell lung cancer with mutation in epidermal growth factor receptor", "shortest_name_length": 76}
{"curie": "UMLS:C0862207", "names": ["Refractory Sezary Syndrome", "Sezary syndrome refractory", "Sezary's disease refractory", "Sezary's syndrome refractory"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sezary syndrome refractory", "shortest_name_length": 26}
{"curie": "UMLS:C0266648", "names": ["blight ovum", "ovum blighted", "blighted ovum", "BLIGHTED OVUM", "Blighted ovum", "blighted ovums", "Resorbed fetus", "Pathologic ovum", "Resorbed foetus", "pathologic; ovum", "ovum; pathologic", "Pre-Embryonic Loss", "anembryonic pregnancy", "Anembryonic Pregnancy", "Anembryonic pregnancy", "Blighted ovum (disorder)", "blighted ovum (diagnosis)", "Empty gestational sac with ongoing pregnancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Blighted ovum", "shortest_name_length": 11}
{"curie": "MONDO:0005016", "names": ["DKD", "DIABETIC NEPHROPATHY", "NEPHROPATHY DIABETIC", "nephropathy diabetic", "diabetic nephropathy", "Diabetic Nephropathy", "Diabetic nephropathy", "Nephropathy;diabetic", "Nephropathy, Diabetic", "diabetic renal disease", "Diabetic nephropathies", "Diabetic renal disease", "Diabetic Nephropathies", "diabetic nephropathies", "Diabetic Kidney Disease", "Diabetic kidney disease", "diabetic kidney disease", "Nephropathies, Diabetic", "Diabetic Kidney Problems", "Kidney Disease, Diabetic", "Diabetic nephropathy NOS", "Diabetic Kidney Diseases", "Kidney Diseases, Diabetic", "type 1 diabetes nephropathy", "type 2 diabetes nephropathy", "DIABETIC RENAL MANIFESTATION", "Diabetic nephropathy syndrome", "diabetic nephropathy (diagnosis)", "Diabetes with renal manifestations", "diabetes with renal manifestations", "diabetes; nephropathy (manifestation)", "nephropathy; diabetes (manifestation)", "Kidney disorder due to diabetes mellitus", "Disorder of kidney due to diabetes mellitus", "diabetes with renal manifestations (diagnosis)", "Renal disorder associated with diabetes mellitus", "Disorder of kidney due to diabetes mellitus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diabetic kidney disease", "shortest_name_length": 3}
{"curie": "UMLS:C0041862", "names": ["Nonpsychotic Mental Disorder Following Organic Brain Damage", "nonpsychotic mental disorder following organic brain damage", "nonpsychotic mental disorder following organic brain damage (diagnosis)", "Unspecified nonpsychotic mental disorder following organic brain damage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unspecified nonpsychotic mental disorder following organic brain damage", "shortest_name_length": 59}
{"curie": "UMLS:C3898764", "names": ["Infiltrating Bladder Urothelial Cancer Associated with Urethral Cancer", "Infiltrating Bladder Urothelial Carcinoma Associated with Urethral Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infiltrating Bladder Urothelial Carcinoma Associated with Urethral Carcinoma", "shortest_name_length": 70}
{"curie": "UMLS:C1335344", "names": ["Paraneoplastic Subacute Sensory Neuropathy", "Paraneoplastic Subacute Sensory Neuronopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paraneoplastic Subacute Sensory Neuronopathy", "shortest_name_length": 42}
{"curie": "UMLS:C0741698", "names": ["Ductal Breast Hyperplasia", "breast ductal hyperplasia", "Breast Ductal Hyperplasia", "BREAST DUCTAL HYPERPLASIA", "Ductal Hyperplasia of Breast", "Breast Epithelial Hyperplasia", "Ductal Hyperplasia of the Breast", "Epithelial Hyperplasia of Breast", "Epithelial Hyperplasia of the Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Ductal Hyperplasia", "shortest_name_length": 25}
{"curie": "MONDO:0020130", "names": ["malformation of the cerebellar vermis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malformation of the cerebellar vermis", "shortest_name_length": 37}
{"curie": "UMLS:C4331318", "names": ["Stage I Oropharyngeal (p16-Negative) Throat Cancer", "Stage I Oropharyngeal (p16-Negative) Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Oropharyngeal (p16-Negative) Carcinoma AJCC v8", "shortest_name_length": 50}
{"curie": "MONDO:0000193", "names": ["CORTRD", "HSD 11B1 deficiency", "Cortisone reductase deficiency", "cortisone reductase deficiency", "deficiency of cortisone reductase", "Deficiency of cortisone reductase", "Deficiency of (R)-20-hydroxysteroid dehydrogenase", "deficiency of (R)-20-hydroxysteroid dehydrogenase", "hyperandrogenism due to cortisone reductase deficiency", "11-beta-hydroxysteroid dehydrogenase deficiency type 1", "11-beta-hydroxysteroid dehydrogenase, type i, deficiency of", "Deficiency of (R)-20-hydroxysteroid dehydrogenase (disorder)", "11-alpha beta-hydroxysteroid dehydrogenase type I deficiency of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cortisone reductase deficiency", "shortest_name_length": 6}
{"curie": "MONDO:0018904", "names": ["MPGN", "Mesangiocapillary glomerulonephritis", "membranoproliferative glomerulonephritis", "primary membranoproliferative glomerulonephritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary membranoproliferative glomerulonephritis", "shortest_name_length": 4}
{"curie": "UMLS:C1707954", "names": ["Estrogen-Producing Adrenal Gland Adenoma", "Estrogen Producing Adrenal Cortex Adenoma", "Estrogen-Producing Adrenal Cortex Adenoma", "Estrogen-Producing Adrenal Cortical Adenoma", "Estrogen Producing Adrenal Cortical Adenoma", "estrogen-producing adrenal cortical adenoma", "estrogen-producing adrenal cortical adenoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "estrogen-producing adrenal cortical adenoma", "shortest_name_length": 40}
{"curie": "MONDO:0021630", "names": ["face lipoma", "face; lipoma", "lipoma; face", "Lipoma of face", "lipoma of face", "Lipoma of skin and subcutaneous tissue of face", "Lipoma of skin and subcutaneous tissue of face (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lipoma of face", "shortest_name_length": 11}
{"curie": "UMLS:C1333149", "names": ["Conjunctival squamous papilloma", "Conjunctival Squamous Papilloma", "Pedunculated conjunctival papilloma", "Conjunctival Squamous Cell Papilloma", "Squamous Cell Papilloma of Conjunctiva", "Squamous Cell Papilloma of the Conjunctiva", "Pedunculated conjunctival papilloma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pedunculated conjunctival papilloma", "shortest_name_length": 31}
{"curie": "MONDO:0012911", "names": ["Php1c", "PHP1C", "Php Ic", "PHP IC", "Php 1C", "pseudohypoparathyroidism Ic", "Pseudohypoparathyroidism type 1C", "Pseudohypoparathyroidism Type 1C", "pseudohypoparathyroidism type 1C", "PSEUDOHYPOPARATHYROIDISM, TYPE IC", "pseudohypoparathyroidism, type IC", "pseudohypoparathyroidism, type 1C", "Pseudohypoparathyroidism, Type Ic", "Pseudohypoparathyroidism type 1C (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudohypoparathyroidism type 1C", "shortest_name_length": 5}
{"curie": "MONDO:0006982", "names": ["THYROIDITIS SUBACUTE", "SUBACUTE THYROIDITIS", "Subacute thyroiditis", "thyroiditis subacute", "Subacute Thyroiditis", "Thyroiditis subacute", "subacute thyroiditis", "thyroiditis; subacute", "THYROIDITIS, SUBACUTE", "subacute; thyroiditis", "Thyroiditis, Subacute", "Subacute Thyroiditides", "DeQuervain thyroiditis", "giant-cell thyroiditis", "Giant cell thyroiditis", "Giant Cell Thyroiditis", "Giant-cell thyroiditis", "DeQuervain Thyroiditis", "Cell Thyroiditis, Giant", "Thyroiditis, Giant Cell", "Thyroiditides, Subacute", "giant cell; thyroiditis", "De Quervain thyroiditis", "de Quervain thyroiditis", "de quervain thyroiditis", "THYROIDITIS, GIANT CELL", "Giant cell thyroiditis,", "thyroiditis de quervain", "thyroiditis; giant cell", "De Quervain Thyroiditis", "dequervain's thyroiditis", "de quervains thyroiditis", "THYROIDITIS, DE QUERVAIN", "Giant Cell Thyroiditides", "de Quervain; thyroiditis", "Thyroiditis, De Quervain", "thyroiditis; de Quervain", "de Quervain's thyroiditis", "Thyroiditides, Giant Cell", "Granulomatous thyroiditis", "De Quervain's thyroiditis", "granulomatous thyroiditis", "Cell Thyroiditides, Giant", "de quervain's thyroiditis", "De Quervain's Thyroiditis", "Granulomatous Thyroiditis", "thyroiditis; granulomatous", "Thyroiditis, Granulomatous", "granulomatous; thyroiditis", "Granulomatous Thyroiditides", "Subacute Painful Thyroiditis", "Thyroiditides, Granulomatous", "Thyroiditis, Subacute Painful", "Painful Thyroiditis, Subacute", "thyroiditis; pseudotuberculous", "THYROIDITIS, PSEUDOTUBERCULOUS", "Subacute Painful Thyroiditides", "pseudotuberculous; thyroiditis", "Thyroiditides, Subacute Painful", "Subacute thyroiditis (disorder)", "Pseudogranulomatous thyroiditis", "Painful Thyroiditides, Subacute", "subacute thyroiditis (diagnosis)", "Subacute Granulomatous Thyroiditis", "Subacute granulomatous thyroiditis", "Subacute Nonsuppurative Thyroiditis", "Thyroiditis, Subacute Nonsuppurative", "Non-suppurative subacute thyroiditis", "Nonsuppurative Thyroiditis, Subacute", "Subacute Nonsuppurative Thyroiditides", "Nonsuppurative Thyroiditides, Subacute", "Thyroiditides, Subacute Nonsuppurative", "Subacute granulomatous thyroiditis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subacute thyroiditis", "shortest_name_length": 20}
{"curie": "MONDO:0054591", "names": ["STISS", "Stankiewicz-Isidor syndrome", "STANKIEWICZ-ISIDOR SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stankiewicz-Isidor syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C3272763", "names": ["Appendix Dysplasia", "Appendiceal Dysplasia", "Appendix Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Appendix Intraepithelial Neoplasia", "shortest_name_length": 18}
{"curie": "MONDO:0004695", "names": ["liver lymphoma", "lymphoma liver", "Liver Lymphoma", "Hepatic lymphoma", "Hepatic Lymphoma", "lymphoma hepatic", "hepatic lymphoma", "Lymphoma of Liver", "lymphoma of liver", "lymphoma of the liver", "Lymphoma of the Liver", "Primary Liver Lymphoma", "primary liver lymphoma", "Primary Hepatic Lymphoma", "primary hepatic lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "liver lymphoma", "shortest_name_length": 14}
{"curie": "UMLS:C0521759", "names": ["Convergence Nystagmus", "nystagmus convergence", "Convergence nystagmus", "convergence nystagmus", "Nystagmus, Convergence", "Convergence nystagmus (disorder)", "convergence nystagmus (diagnosis)", "convergence nystagmus (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Convergence Nystagmus", "shortest_name_length": 21}
{"curie": "UMLS:C5557313", "names": ["DS Stage IIA Plasma Cell Myeloma", "Durie/Salmon Stage IIA Plasma Cell Myeloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DS Stage IIA Plasma Cell Myeloma", "shortest_name_length": 32}
{"curie": "MONDO:0009039", "names": ["BGS", "Baller-Gerold syndrome", "BALLER-GEROLD SYNDROME", "baller-gerold syndrome", "baller gerold syndrome", "BALLER-Gerold syndrome", "Baller-Gerold syndrome (BGS)", "Baller-Gerold syndrome (disorder)", "CRANIOSYNOSTOSIS WITH RADIAL DEFECTS", "craniosynostosis with radial defects", "Craniosynostosis with radial defects", "Craniosynostosis radial aplasia syndrome", "Craniosynostosis-Radial Aplasia Syndrome", "CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME", "Craniosynostosis-radial aplasia syndrome", "craniosynostosis-radial aplasia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Baller-Gerold syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0021964", "names": ["Bagatelle Cassidy syndrome", "bagatelle Cassidy syndrome", "macrocephaly short limbs deafness", "Macrocephaly short limbs deafness", "macrocephaly, hypertelorism, short limbs, hearing loss, and developmental delay", "Macrocephaly, hypertelorism, short limbs, hearing loss, and developmental delay"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bagatelle Cassidy syndrome", "shortest_name_length": 26}
{"curie": "UMLS:C0162494", "names": ["Parasitic Pregnancy Complication", "Complication, Parasitic Pregnancy", "Parasitic Complications Pregnancy", "Pregnancy Complication, Parasitic", "Parasitic Pregnancy Complications", "Pregnancy, Parasitic Complications", "Complications, Parasitic Pregnancy", "Complications Pregnancy, Parasitic", "Pregnancy Complications, Parasitic", "Parasitic Complications Pregnancies", "Complications Pregnancies, Parasitic", "Pregnancies, Parasitic Complications"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pregnancy Complications, Parasitic", "shortest_name_length": 32}
{"curie": "MONDO:0032747", "names": ["HYDM4", "hydatidiform mole, recurrent, 4", "HYDATIDIFORM MOLE, RECURRENT, 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hydatidiform mole, recurrent, 4", "shortest_name_length": 5}
{"curie": "MONDO:0011226", "names": ["DFNA15", "autosomal dominant deafness 15", "deafness, autosomal dominant 15", "Deafness, Autosomal Dominant 15", "DEAFNESS, AUTOSOMAL DOMINANT 15", "deafness, autosomal dominant type 15", "autosomal dominant nonsyndromic deafness 15", "autosomal dominant nonsyndromic hearing loss 15", "POU4F3 autosomal dominant nonsyndromic deafness", "autosomal dominant nonsyndromic deafness type 15", "autosomal dominant nonsyndromic deafness caused by mutation in POU4F3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 15", "shortest_name_length": 6}
{"curie": "MONDO:0004788", "names": ["cervix squamous papilloma", "Cervix Squamous Papilloma", "Cervical Squamous Papilloma", "cervical squamous papilloma", "Squamous Papilloma of Cervix", "squamous papilloma of cervix", "Cervix Uteri Squamous Papilloma", "cervix uteri squamous papilloma", "squamous papilloma of the cervix", "Squamous Papilloma of the Cervix", "Cervical Squamous Cell Papilloma", "uterine cervix squamous papilloma", "Uterine Cervix Squamous Papilloma", "squamous papilloma of cervix uteri", "Squamous Papilloma of Cervix Uteri", "Squamous Papilloma of Uterine Cervix", "squamous papilloma of uterine cervix", "squamous papilloma of the Cervix Uteri", "Squamous Papilloma of the Cervix Uteri", "squamous papilloma of the cervix uteri", "squamous papilloma of the uterine cervix", "Squamous Papilloma of the Uterine Cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervix squamous papilloma", "shortest_name_length": 25}
{"curie": "UMLS:C4727088", "names": ["Advanced Lung Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Lung Carcinoma", "shortest_name_length": 23}
{"curie": "UMLS:C5557381", "names": ["Vaginal Smooth Muscle Tumor of Uncertain Malignant Potential", "Vaginal Smooth Muscle Neoplasm of Uncertain Malignant Potential"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Smooth Muscle Tumor of Uncertain Malignant Potential", "shortest_name_length": 60}
{"curie": "MONDO:0022500", "names": ["arthrogryposis multiplex congenita CNS calcification"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis multiplex congenita CNS calcification", "shortest_name_length": 52}
{"curie": "OMIM:612560", "names": ["BMND12", "BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 6}
{"curie": "MONDO:0003941", "names": ["Classic Variant of Chromophobe Renal Cell Carcinoma", "classic variant of chromophobe renal cell carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "classic variant of chromophobe renal cell carcinoma", "shortest_name_length": 51}
{"curie": "MONDO:0019818", "names": ["cleft mitral valve"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleft mitral valve", "shortest_name_length": 18}
{"curie": "UMLS:C0855085", "names": ["Recurrent Hodgkin's Nodular Sclerosis", "Recurrent Nodular Sclerosis Hodgkin Lymphoma", "Relapsed Nodular Sclerosis Hodgkin's Disease", "Recurrent Nodular Sclerosis Hodgkin's Disease", "Hodgkin's disease nodular sclerosis recurrent", "Relapsed Nodular Sclerosis Hodgkin's Lymphoma", "Recurrent Nodular Sclerosis Hodgkin's Lymphoma", "Recurrent Nodular Sclerosis Classic Hodgkin Lymphoma", "Recurrent Nodular Sclerosis Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's disease nodular sclerosis recurrent", "shortest_name_length": 37}
{"curie": "MONDO:0012287", "names": ["STICKLER SYNDROME, ATYPICAL", "Stickler Syndrome, Atypical", "Stickler syndrome, atypical", "STICKLER SYNDROME, TYPE I, NONSYNDROMIC OCULAR", "Stickler Syndrome, Type I, Nonsyndromic Ocular", "Stickler syndrome, type I, nonsyndromic ocular", "Stickler syndrome, type i, nonsyndromic ocular", "STICKLER SYNDROME, TYPE I, PREDOMINANTLY OCULAR", "Stickler syndrome, type I, predominantly ocular", "Stickler Syndrome, Type I, Predominantly Ocular", "rhegmatogenous retinal detachment, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stickler syndrome, type I, nonsyndromic ocular", "shortest_name_length": 27}
{"curie": "MONDO:0002062", "names": ["Breast Myofibroblastoma", "breast myofibroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast myofibroblastoma", "shortest_name_length": 23}
{"curie": "MONDO:0800136", "names": ["non-severe combined immunodeficiency due to COPG1 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-severe combined immunodeficiency due to COPG1 deficiency", "shortest_name_length": 60}
{"curie": "UMLS:C0155713", "names": ["Papillary muscle rupture", "papillary muscle rupture", "rupture; papillary muscle", "papillary muscle; rupture", "Ruptured papillary muscle", "rupture of papillary muscle", "Rupture of papillary muscle", "Rupture of papillary muscle (disorder)", "rupture of papillary muscle (diagnosis)", "complications heart disease rupture papillary muscle"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rupture of papillary muscle", "shortest_name_length": 24}
{"curie": "UMLS:C0221714", "names": ["Infection injection site", "INFECTION INJECTION SITE", "INJECTION SITE INFECTION", "Injection site infection", "injection site infection", "Injection site infection (disorder)", "local infection following injection", "Injection site infection (diagnosis)", "local infection following injection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site infection", "shortest_name_length": 24}
{"curie": "UMLS:C4289908", "names": ["Broad Ligament Serous Cystadenofibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Broad Ligament Serous Cystadenofibroma", "shortest_name_length": 38}
{"curie": "MONDO:0010114", "names": ["Thanatophoric dysplasia Glasgow variant", "thanatophoric dysplasia, Glasgow variant", "Thanatophoric Dysplasia, Glasgow Variant", "THANATOPHORIC DYSPLASIA, GLASGOW VARIANT", "NEONATALLY LETHAL SHORT-LIMB SKELETAL DYSPLASIA, GLASGOW TYPE", "neonatally lethal short-limb skeletal dysplasia, Glasgow type", "Neonatally lethal short-limb skeletal dysplasia, glasgow type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thanatophoric dysplasia, Glasgow variant", "shortest_name_length": 39}
{"curie": "MONDO:0010944", "names": ["MSF", "mitochondrial import-stimulating factor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial import-stimulating factor", "shortest_name_length": 3}
{"curie": "UMLS:C4682697", "names": ["Refractory Transformed Lymphoma", "Refractory Transformed Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Transformed Non-Hodgkin Lymphoma", "shortest_name_length": 31}
{"curie": "MONDO:0004365", "names": ["Uveal Necrotic Melanoma", "Necrotic Uveal Melanoma", "necrotic uveal melanoma", "necrotic intraocular melanoma", "Necrotic intraocular melanoma", "intraocular melanoma, necrotic", "melanoma, necrotic intraocular", "melanoma, intraocular, necrotic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "necrotic uveal melanoma", "shortest_name_length": 23}
{"curie": "MONDO:0014255", "names": ["CFBD", "complement factor b deficiency", "COMPLEMENT FACTOR B DEFICIENCY", "complement factor B deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complement factor b deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0014630", "names": ["FAP3", "NTHL1-related AFAP", "NTHL1-related attenuated FAP", "FAMILIAL ADENOMATOUS POLYPOSIS 3", "familial adenomatous polyposis 3", "familial adenomatous polyposis type 3", "NTHL1-related attenuated familial adenomatous polyposis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial adenomatous polyposis 3", "shortest_name_length": 4}
{"curie": "UMLS:C0153299", "names": ["infection by Ancylostoma braziliense", "Ancylostomiasis due to Ancylostoma Braziliense", "Ancylostomiasis due to ancylostoma braziliense", "Ancylostomiasis due to Ancylostoma braziliense", "infection by Ancylostoma braziliense (diagnosis)", "Ancylostomiasis caused by Ancylostoma braziliense", "Ancylostomiasis due to Ancylostoma braziliense (disorder)", "Ancylostomiasis caused by Ancylostoma braziliense (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ancylostomiasis due to Ancylostoma braziliense (disorder)", "shortest_name_length": 36}
{"curie": "MONDO:0015016", "names": ["ASGD6", "anterior segment dysgenesis 6", "ANTERIOR SEGMENT DYSGENESIS 6", "anterior segment dysgenesis type 6", "anterior segment dysgenesis 6, multiple subtypes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anterior segment dysgenesis 6", "shortest_name_length": 5}
{"curie": "UMLS:C5446614", "names": ["Metastatic Primary Malignant Brain Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Primary Malignant Brain Neoplasm", "shortest_name_length": 43}
{"curie": "MONDO:0015256", "names": ["Rodini-Richieri Costa syndrome", "blepharoptosis-cleft palate-ectrodactyly-dental anomalies syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blepharoptosis-cleft palate-ectrodactyly-dental anomalies syndrome", "shortest_name_length": 30}
{"curie": "MONDO:0006733", "names": ["kc", "kcs", "KCS", "Dry Eye", "dry eye", "Dry eye", "DRY EYES", "Dry eyes", "dry eye(s)", "Dry Eye(s)", "eye(s), dry", "Xerophthalmia", "Keratitis sicca", "keratitis sicca", "sicca keratitis", "Dry Eye Disease", "dry eye disease", "Dry Eye Syndrome", "syndrome dry eye", "Dry Eye Diseases", "Dry eye syndrome", "dry eye syndrome", "dry eyes syndrome", "Dry Eye Syndromes", "Dry eye syndromes", "dry eye; syndrome", "syndrome; dry eye", "dry eye syndromes", "Tear film deficiency", "Tear film insufficiency", "tear film insufficiency", "Keratoconjunctivitis sicca", "Keratoconjunctivitis Sicca", "keratoconjunctivitis sicca", "KERATOCONJUNCTIVITIS SICCA", "kerato conjunctivitis sicca", "Sicca, Keratoconjunctivitis", "sicca, keratoconjunctivitis", "Kerato conjunctivitis sicca", "dry eye syndrome (diagnosis)", "KCS - Keratoconjunctivitis sicca", "Keratoconjunctivitis sicca (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dry eye syndrome", "shortest_name_length": 2}
{"curie": "UMLS:C4521613", "names": ["Stage I Bone Cancer", "Stage I Bone Cancer AJCC v8", "Stage I Appendicular Skeleton, Trunk, Skull, and Facial Bones Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Bone Cancer AJCC v8", "shortest_name_length": 19}
{"curie": "MONDO:0011072", "names": ["T2D2", "NIDDM2", "TYPE 2 DIABETES MELLITUS 2", "Noninsulin-Dependent Diabetes Mellitus 2", "noninsulin-dependent diabetes mellitus 2", "NONINSULIN-DEPENDENT DIABETES MELLITUS 2", "DIABETES MELLITUS, NONINSULIN-DEPENDENT, 2", "diabetes mellitus, noninsulin-dependent, 2", "Diabetes Mellitus, Noninsulin-Dependent, 2", "DIABETES MELLITUS, NONINSULIN-DEPENDENT, 2 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diabetes mellitus, noninsulin-dependent, 2", "shortest_name_length": 4}
{"curie": "UMLS:C2350170", "names": ["Unilateral Nasal Obstruction", "Nasal Obstruction, Unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unilateral Nasal Obstruction", "shortest_name_length": 28}
{"curie": "UMLS:C0264734", "names": ["Atrium dilated", "Dilated atrium", "Atrial dilation", "atrial dilatation", "Atrial dilatation", "dilatation atrial", "Dilatation atrial", "Atrial dilatation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atrial dilatation", "shortest_name_length": 14}
{"curie": "MONDO:0002710", "names": ["Infiltrating Angiolipoma", "Infiltrating angiolipoma", "infiltrating angiolipoma", "angiolipoma, infiltrating", "Angiolipoma, infiltrating", "angiolipoma, infiltrating (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infiltrating angiolipoma", "shortest_name_length": 24}
{"curie": "MONDO:0015396", "names": ["larynx cyst", "cyst; larynx", "cysts larynx", "larynx; cyst", "Laryngeal cyst", "Cyst of larynx", "laryngeal cyst", "cysts laryngeal", "congenital; cyst, larynx", "cyst; congenital, larynx", "Congenital laryngeal cyst", "Cyst of larynx (disorder)", "congenital laryngeal cyst", "Congenital cyst of larynx", "Congenital cyst of larynx (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital laryngeal cyst", "shortest_name_length": 11}
{"curie": "UMLS:C0237962", "names": ["retroperitoneal abscess", "Retroperitoneal abscess", "RETROPERITONEAL ABSCESS", "Retroperitoneal Abscess", "retroperitoneal; abscess", "abscess; retroperitoneal", "ABSCESS, RETROPERITONEAL", "Retroperitoneal abscess (disorder)", "retroperitoneal abscess (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retroperitoneal abscess", "shortest_name_length": 23}
{"curie": "MONDO:0015855", "names": ["isolated congenital amastia", "isolated congenital breast hypoplasia/aplasia", "breasts and/or nipples, aplasia or hypoplasia of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated congenital breast hypoplasia/aplasia", "shortest_name_length": 27}
{"curie": "UMLS:C1333324", "names": ["Dysplasia in Barrett Esophagus", "Dysplasia in Barrett's Esophagus", "Barretts esophagus with dysplasia", "Barretts oesophagus with dysplasia", "Barrett's esophagus with dysplasia", "Barretts esophagus with dysplasia (disorder)", "Barrett's esophagus with dysplasia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Barretts esophagus with dysplasia", "shortest_name_length": 30}
{"curie": "MONDO:0007696", "names": ["Emery-Nelson syndrome", "hand and foot deformity - flat facies", "Hand and foot deformity with flat facies", "hand and foot deformity with flat facies", "HAND AND FOOT DEFORMITY WITH FLAT FACIES", "hand and foot deformity-flat facies syndrome", "familial syndrome of short stature, deformities of the hands and feet, and unusual facies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Emery-Nelson syndrome", "shortest_name_length": 21}
{"curie": "UMLS:C1541447", "names": ["Recurrent Grade III Lymphomatoid Granulomatosis", "recurrent childhood grade III lymphomatoid granulomatosis", "Recurrent Childhood Grade III Lymphomatoid Granulomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Grade III Lymphomatoid Granulomatosis", "shortest_name_length": 47}
{"curie": "MONDO:0008497", "names": ["YPS", "STRMK", "Stormorken Syndrome", "Stormorken syndrome", "STORMORKEN SYNDROME", "york Platelet syndrome", "YORK PLATELET SYNDROME", "Thrombocytopathy asplenia miosis", "Thrombocytopathy, asplenia and miosis", "thrombocytopathy, asplenia and miosis", "Stormorken-Sjaastad-Langslet syndrome", "THROMBOCYTOPATHY, ASPLENIA, AND MIOSIS", "Thrombocytopathy, Asplenia, and Miosis", "Thrombocytopathy, asplenia, and miosis", "Thrombocytopathy-asplenia-miosis syndrome", "Thrombocytopathy, asplenia and miosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stormorken syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C1266009", "names": ["Trichilemmocarcinoma", "Trichilemmal Carcinoma", "Trichilemmal carcinoma", "Trichilemmal carcinoma (disorder)", "Trichilemmal carcinoma (diagnosis)", "skin neoplasm malignant trichilemmal carcinoma", "Trichilemmocarcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Trichilemmal carcinoma", "shortest_name_length": 20}
{"curie": "MONDO:0017377", "names": ["Pfeiffer Mayer syndrome", "Pfeiffer-Mayer syndrome", "preaxial polydactyly-colobomata-intellectual disability syndrome", "Preaxial polydactyly-colobomata-intellectual disability syndrome", "Preaxial polydactyly, colobomata, intellectual disability syndrome", "preaxial polydactyly, colobomata, intellectual disability syndrome", "Preaxial polydactyly, colobomata, intellectual disability syndrome (disorder)", "preaxial polydactyly, colobomata, intellectual disability syndrome (diagnosis)", "short stature mental retardation type I preaxial polydactyly with colobomatous abnormalities", "short stature intellectual disability type I preaxial polydactyly with colobomatous abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "preaxial polydactyly-colobomata-intellectual disability syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0016293", "names": ["Congenital night blindness", "Night blindness, congenital", "Night blindness since birth", "Night blindness, stationary", "Static congenital hemeralopia", "Congenital essential nyctalopia", "congenital essential nyctalopia", "Congenital stationary night blindness", "congenital stationary night blindness", "night blindness, congenital stationary", "Night blindness, congenital stationary", "CSNB - Congenital stationary night blindness", "Congenital stationary night blindness (disorder)", "Night blindness, congenital stationary, complete", "congenital stationary night blindness (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital stationary night blindness", "shortest_name_length": 26}
{"curie": "MONDO:0006479", "names": ["OGCT of pancreas", "Pancreatic osteoclastic giant cell tumor", "pancreatic osteoclastic giant cell tumor", "osteoclastic giant cell tumor of pancreas", "Osteoclastic giant cell tumor of pancreas", "osteoclast-like giant cell neoplasm of pancreas", "pancreatic osteoclast-like giant cell carcinoma", "Osteoclast-like Giant Cell Neoplasm of Pancreas", "Osteoclast-like Giant cell neoplasm of pancreas", "Pancreatic Osteoclast-Like Giant Cell Carcinoma", "Osteoclast-like Giant Cell Neoplasm of the Pancreas", "osteoclast-like giant cell neoplasm of the pancreas", "pancreatic carcinoma with osteoclast-like giant cells", "carcinoma of pancreas with osteoclast-like giant cells", "Undifferentiated carcinoma with osteoclast-like giant cells", "carcinoma of pancreas with osteoclast-like giant cells (diagnosis)", "pancreatic undifferentiated carcinoma with osteoclast-like giant cells", "undifferentiated pancreatic carcinoma with osteoclast-like giant cells", "Pancreatic Undifferentiated Carcinoma with Osteoclast-Like Giant Cells", "Pancreatic undifferentiated carcinoma with osteoclast-like giant cells", "Undifferentiated Pancreatic Carcinoma with Osteoclast-Like Giant Cells", "Undifferentiated carcinoma of pancreas with osteoclast-like giant cells", "undifferentiated carcinoma of pancreas with osteoclast-like giant cells"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "undifferentiated pancreatic carcinoma with osteoclast-like giant cells", "shortest_name_length": 16}
{"curie": "MONDO:0012611", "names": ["PMSE", "PMSE SYNDROME", "PMSE syndrome", "pretzel syndrome", "polyhydramnios, megalencephaly, and symptomatic epilepsy", "Polyhydramnios, Megalencephaly, And Symptomatic Epilepsy", "POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY", "Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome", "polyhydramnios-megalencephaly-symptomatic epilepsy syndrome", "Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome", "polyhydramnios, megalencephaly, and symptomatic epilepsy syndrome", "PMSE (polyhydramnios, megalencephaly, symptomatic epilepsy) syndrome", "Polyhydramnios, megalencephaly, symptomatic epilepsy syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyhydramnios, megalencephaly, and symptomatic epilepsy", "shortest_name_length": 4}
{"curie": "UMLS:C2200127", "names": ["Lung Neuroendocrine Carcinoma", "neuroendocrine carcinoma of lung", "High Grade Lung Neuroendocrine Neoplasm", "neuroendocrine carcinoma of lung (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuroendocrine carcinoma of lung", "shortest_name_length": 29}
{"curie": "UMLS:C0282074", "names": ["Bile sludging", "Biliary Sludge", "biliary sludge", "Biliary sludge", "BILIARY SLUDGE", "Sludge, Biliary", "Biliary sludge (disorder)", "biliary sludge (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Biliary Sludge", "shortest_name_length": 13}
{"curie": "MONDO:0016375", "names": ["acquired peripheral movement disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired peripheral movement disorder", "shortest_name_length": 37}
{"curie": "MONDO:0020669", "names": ["NASAL SINUS CANCER", "cancer nasal sinus", "nasal sinus cancer", "Nasal sinus cancer", "paranasal sinus cancer", "Malignant Accessory Sinus Tumor", "malignant accessory sinus tumor", "malignant paranasal sinus tumor", "Malignant Paranasal Sinus Tumor", "Malignant tumor of nasal sinuses", "Malignant tumour of nasal sinuses", "malignant tumor of paranasal sinus", "Malignant Accessory Sinus Neoplasm", "Malignant Tumor of Paranasal Sinus", "Malignant Paranasal Sinus Neoplasm", "malignant accessory sinus neoplasm", "Malignant Tumor of Accessory Sinus", "malignant paranasal sinus neoplasm", "malignant tumor of accessory sinus", "Malignant Neoplasm of Accessory Sinus", "Malignant Neoplasm of Paranasal Sinus", "malignant neoplasm of paranasal sinus", "malignant neoplasm of accessory sinus", "malignant tumor of the accessory sinus", "Malignant Tumor of the Accessory Sinus", "Malignant Tumor of the Paranasal Sinus", "malignant tumor of the paranasal sinus", "Malignant neoplasm of accessory sinuses", "malignant neoplasm of the paranasal sinus", "Malignant Neoplasm of the Paranasal Sinus", "malignant neoplasm of the accessory sinus", "Malignant Neoplasm of the Accessory Sinus", "Malignant neoplasm of accessory sinus, NOS", "Malignant tumor of nasal sinuses (disorder)", "malignant neoplasm of accessory sinus (diagnosis)", "Malignant neoplasm of accessory sinus, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paranasal sinus cancer", "shortest_name_length": 18}
{"curie": "UMLS:C5206782", "names": ["Non-M3 Acute Myeloid Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-M3 Acute Myeloid Leukemia", "shortest_name_length": 29}
{"curie": "MONDO:0027048", "names": ["DFNY2", "Y-linked deafness 2", "DEAFNESS, Y-LINKED 2", "deafness, Y-linked 2", "deafness, y-linked 2, y-linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness, Y-linked 2", "shortest_name_length": 5}
{"curie": "MONDO:0015313", "names": ["choanal atresia, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choanal atresia, bilateral", "shortest_name_length": 26}
{"curie": "UMLS:C5419584", "names": ["Refractory Grade 3a Follicular Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Grade 3a Follicular Lymphoma", "shortest_name_length": 39}
{"curie": "MONDO:0012877", "names": ["MAFD8", "MAJOR affective disorder 8", "MAJOR AFFECTIVE DISORDER 8", "BIPOLAR AFFECTIVE DISORDER", "bipolar affective disorder", "Major Affective Disorder 8", "major affective disorder 8", "major affective disorder-8, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "major affective disorder 8", "shortest_name_length": 5}
{"curie": "MONDO:0008199", "names": ["PD", "LOPD", "PARK", "late-onset Parkinson disease", "Parkinson disease late onset", "late onset Parkinson disease", "Parkinson disease, late-onset", "Parkinson disease, late onset", "PARKINSON DISEASE, LATE-ONSET", "late onset Parkinson's disease", "hereditary late onset Parkinson disease", "Hereditary late onset Parkinson disease", "Hereditary late-onset Parkinson disease", "hereditary late-onset Parkinson disease", "Parkinson disease, late onset (diagnosis)", "Autosomal dominant late onset Parkinson disease", "autosomal dominant late-onset Parkinson disease", "Parkinson disease autosomal dominant late onset", "Autosomal dominant late-onset Parkinson disease", "Parkinson disease, susceptibility to, Multifactorial", "Parkinson disease, age of onset, modifier, Multifactorial", "Autosomal dominant late onset Parkinson disease (disorder)", "Autosomal dominant late onset Parkinson disease (diagnosis)", "Parkinson disease, late-onset, susceptibility to, Multifactorial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "late-onset Parkinson disease", "shortest_name_length": 2}
{"curie": "MONDO:0000022", "names": ["ENUR1", "wet bed", "bed wet", "bed wets", "wets bed", "Wets bed", "enuresis", "BEDWETTING", "bedwetting", "Bedwetting", "bed-wetting", "wetting bed", "Bed wetting", "BED WETTING", "bed wetting", "sleep enuresis", "Sleep Enuresis", "Enuresis nocturna", "NOCTURNAL ENURESIS", "Nocturnal enuresis", "enuresis nocturnal", "Nocturnal Enuresis", "nocturnal enuresis", "Enuresis, Nocturnal", "enuresis; nocturnal", "bedwetting/enuresis", "Enuresis, nocturnal", "bedwetting enuresis", "nocturnal; enuresis", "enuresis bedwetting", "Bedwetting/enuresis", "enuresis, nocturnal", "ENURESIS, NOCTURNAL, 1", "Nocturnal only enuresis", "Nocturnal enuresis (finding)", "Nighttime Urinary Incontinence", "nocturnal enuresis (diagnosis)", "Urinary Incontinence, Nighttime", "Nocturnal incontinence of urine", "Incontinence, Nighttime Urinary", "Bedwetting/enuresis (excluding U04)", "unable to restrain urination at night while asleep", "unable to restrain urination at night while asleep (symptom)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nocturnal enuresis", "shortest_name_length": 5}
{"curie": "UMLS:C4724834", "names": ["Locally Advanced Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Carcinoma", "shortest_name_length": 26}
{"curie": "UMLS:C0278884", "names": ["Recurrent Melanoma", "melanoma recurrent", "Melanoma recurrent", "recurrent melanoma", "melanoma, recurrent", "Recurrent Melanoma of Skin", "recurrent cutaneous melanoma", "Recurrent Malignant Melanoma", "Recurrent Cutaneous Melanoma", "melanoma, cutaneous recurrent", "cutaneous melanoma, recurrent", "Recurrent Melanoma of the Skin", "Recurrent Malignant Skin Melanoma", "Recurrent Cutaneous (Skin) Melanoma", "Recurrent Malignant Melanoma of Skin", "Recurrent Malignant Melanoma of the Skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Melanoma recurrent", "shortest_name_length": 18}
{"curie": "MONDO:0002206", "names": ["sweat gland cancer", "cancer of sweat gland", "Malignant sweat gland tumor", "Sweat gland tumor, malignant", "Malignant sweat gland tumour", "Sweat gland tumour, malignant", "Malignant Tumor of Sweat Gland", "malignant tumor of sweat gland", "malignant sweat gland neoplasm", "Malignant sweat gland neoplasm", "Malignant Sweat Gland Neoplasm", "Sweat Gland Neoplasms, Malignant", "sweat gland neoplasms, malignant", "Malignant Neoplasm of Sweat Gland", "Malignant neoplasm of sweat gland", "malignant neoplasm of sweat gland", "malignant tumor of the sweat gland", "Malignant Tumor of the Sweat Gland", "malignant tumor of the Sweat gland", "malignant neoplasm of sweat glands", "malignant neoplasm of the sweat gland", "Malignant Neoplasm of the Sweat Gland", "malignant neoplasm of sweat gland (diagnosis)", "neoplasm of integumentary system sweat gland malignant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sweat gland cancer", "shortest_name_length": 18}
{"curie": "MONDO:0011197", "names": ["hereditary thermosensitive neuropathy", "Hereditary thermosensitive neuropathy", "Neuropathy, Hereditary Thermosensitive", "NEUROPATHY, HEREDITARY THERMOSENSITIVE", "neuropathy, hereditary thermosensitive", "Hereditary thermosensitive neuropathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary thermosensitive neuropathy", "shortest_name_length": 37}
{"curie": "MONDO:0013673", "names": ["WFSL", "Wolfram-like syndrome", "Wolfram-like syndrome (disorder)", "Wolfram-like syndrome (diagnosis)", "autosomal dominant Wolfram syndrome", "Wolfram-Like Syndrome, Autosomal Dominant", "Wolfram-like syndrome, autosomal dominant", "WOLFRAM-LIKE SYNDROME, AUTOSOMAL DOMINANT", "inherited genetic conditions autosomal dominant Wolfram-like syndrome", "hearing loss, progressive, with optic atrophy and/or impaired glucose Regulation", "HEARING LOSS, PROGRESSIVE, WITH OPTIC ATROPHY AND/OR IMPAIRED GLUCOSE REGULATION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wolfram-like syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0342313", "names": ["Hypoglycemic state in diabetes", "Hypoglycaemic state in diabetes", "Hypoglycemia due to diabetes mellitus", "Hypoglycaemia due to diabetes mellitus", "Hypoglycemic state due to diabetes mellitus", "Hypoglycaemic state due to diabetes mellitus", "Hypoglycemia due to diabetes mellitus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypoglycemia due to diabetes mellitus", "shortest_name_length": 30}
{"curie": "MONDO:0009007", "names": ["Jalili syndrome", "JALILI SYNDROME", "cone-rod dystrophy amelogenesis imperfecta", "Cone-Rod Dystrophy And Amelogenesis Imperfecta", "CONE-ROD DYSTROPHY AND AMELOGENESIS IMPERFECTA", "cone-rod dystrophy and amelogenesis imperfecta", "cone-rod dystrophy with amelogenesis imperfecta", "cone rod dystrophy-amelogenesis imperfecta syndrome", "Cone rod dystrophy-amelogenesis imperfecta syndrome", "Amelogenesis imperfecta co-occurrent with cone rod dystrophy", "Amelogenesis imperfecta co-occurrent with cone rod dystrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jalili syndrome", "shortest_name_length": 15}
{"curie": "UMLS:C1699324", "names": ["Pharyngeal Mucositis", "Pharyngeal mucositis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pharyngeal Mucositis", "shortest_name_length": 20}
{"curie": "UMLS:C0238156", "names": ["Hematoma, Subdural, Cranial", "Intracranial subdural hematoma", "Intracranial Subdural Hematoma", "INTRACRANIAL SUBDURAL HEMATOMA", "Hematoma, Intracranial Subdural", "Intracranial Subdural Hematomas", "Intracranial subdural haematoma", "Subdural Hematoma, Intracranial", "Hematoma, Subdural, Intracranial", "HEMATOMA, SUBDURAL, INTRACRANIAL", "Subdural Hematomas, Intracranial", "Hematomas, Intracranial Subdural", "PACHYMENINGITIS, HEMORRHAGIC INTERNAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hematoma, Subdural, Intracranial", "shortest_name_length": 27}
{"curie": "UMLS:C0751198", "names": ["Hepatic Stupor", "Hepatic Stupors", "Stupor, Hepatic", "Stupors, Hepatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatic Stupor", "shortest_name_length": 14}
{"curie": "UMLS:C0376338", "names": ["diagnosis psychiatric", "Psychiatric Diagnosis", "psychiatric diagnosis", "Diagnosis, Psychiatric"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diagnosis, Psychiatric", "shortest_name_length": 21}
{"curie": "UMLS:C4054087", "names": ["Refluxing Megaureter", "Refluxing Non-Obstructed Megaureter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refluxing Megaureter", "shortest_name_length": 20}
{"curie": "MONDO:0019207", "names": ["DEND syndrome", "DEND Syndrome", "Developmental Delay, Epilepsy, and Neonatal Diabetes", "developmental delay-epilepsy-neonatal diabetes syndrome", "Developmental delay-epilepsy-neonatal diabetes syndrome", "Developmental delay, epilepsy, neonatal diabetes syndrome", "DEND (developmental delay, epilepsy, neonatal diabetes) syndrome", "neonatal diabetes mellitus, developmental delay, epilepsy syndrome", "Developmental delay, epilepsy, neonatal diabetes syndrome (disorder)", "K ATP associated developmental delay, epilepsy and neonatal diabetes", "K ATP Associated Developmental Delay, Epilepsy and Neonatal Diabetes", "neonatal diabetes mellitus, developmental delay, epilepsy syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DEND syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0010498", "names": ["MEND", "MEND syndrome", "MEND SYNDROME", "MEND syndrome, X-linked recessive", "MALE EBP DISORDER WITH NEUROLOGIC DEFECTS", "Male EBP disorder with neurologic defects", "Male EBP disorder with neurological defects", "male EBP disorder with neurological defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MEND syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C1711322", "names": ["Atypical Mesothelial Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypical Mesothelial Hyperplasia", "shortest_name_length": 32}
{"curie": "MONDO:0016815", "names": ["Leigh disease with leukodystrophy", "Leigh syndrome with leukodystrophy", "infantile subacute necrotizing encephalopathy with leukodystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leigh syndrome with leukodystrophy", "shortest_name_length": 33}
{"curie": "UMLS:C2986660", "names": ["Stage 0 Paranasal Sinus Cancer", "Stage 0 Paranasal Sinus Cancer AJCC v8", "Stage 0 Paranasal Sinus Cancer AJCC v6", "Stage 0 Paranasal Sinus Cancer AJCC v7", "stage 0 maxillary sinus carcinoma in situ", "Stage 0 Paranasal Sinus Cancer AJCC v6, v7, and v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Paranasal Sinus Cancer AJCC v6, v7, and v8", "shortest_name_length": 30}
{"curie": "UMLS:C2986875", "names": ["Thymic Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thymic Hodgkin Lymphoma", "shortest_name_length": 23}
{"curie": "UMLS:C0280182", "names": ["Relapsed Grade I Follicular Lymphoma", "recurrent grade 1 follicular lymphoma", "Recurrent Grade 1 Follicular Lymphoma", "Recurrent Grade I Follicular Lymphoma", "Relapsed Follicular Small Cleaved Cell Lymphoma", "relapsed follicular small cleaved cell lymphoma", "follicular small cleaved cell lymphoma, relapsed", "Recurrent Follicular Small Cleaved Cell Lymphoma", "follicular small cleaved cell lymphoma, recurrent", "Relapsed Grade I Follicular Small Cleaved Cell Lymphoma", "recurrent grade I follicular small cleaved cell lymphoma", "Recurrent Grade I Follicular Small Cleaved Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Grade 1 Follicular Lymphoma", "shortest_name_length": 36}
{"curie": "UMLS:C1336925", "names": ["AIDS-Related Gastric Kaposi Sarcoma", "AIDS-Related Gastric Kaposi's Sarcoma", "AIDS-Related Kaposi's Sarcoma of Stomach", "AIDS-Related Kaposi's Sarcoma of the Stomach"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Gastric Kaposi Sarcoma", "shortest_name_length": 35}
{"curie": "UMLS:C4329373", "names": ["Autonomous Ovarian Follicular Cyst"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Autonomous Ovarian Follicular Cyst", "shortest_name_length": 34}
{"curie": "MONDO:0018511", "names": ["appendiceal epithelial tumor", "epithelial tumor of the appendix", "vermiform appendix epithelial neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epithelial tumor of the appendix", "shortest_name_length": 28}
{"curie": "UMLS:C5447401", "names": ["PALB2-Mutated Malignant Neoplasm", "PALB2-Associated Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PALB2-Associated Malignant Neoplasm", "shortest_name_length": 32}
{"curie": "MONDO:0012186", "names": ["FANCI", "Fanconi anemia complementation group I", "Fanconi Anemia, complementation Group 1", "FANCONI ANEMIA, COMPLEMENTATION GROUP I", "Fanconi Anemia, Complementation Group I", "Fanconi anemia, complementation group I", "Fanconi anemia complementation group type I", "Fanconi Anemia, complementation group type 1", "Fanconi anemia complementation group I (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fanconi anemia complementation group I", "shortest_name_length": 5}
{"curie": "UMLS:C2887091", "names": ["Sepsis due to Hemophilus influenzae", "Sepsis due to Haemophilus influenzae", "Sepsis caused by Haemophilus influenzae", "Sepsis caused by Haemophilus influenzae (disorder)", "Severe sepsis with acute organ dysfunction caused by Haemophilus influenzae"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sepsis caused by Haemophilus influenzae", "shortest_name_length": 35}
{"curie": "MONDO:0012784", "names": ["ARCA2", "SCAR9", "COQ10D4", "primary coenzyme Q10 deficiency 4", "coenzyme Q10 deficiency, primary, 4", "COENZYME Q10 DEFICIENCY, PRIMARY, 4", "coenzyme Q10 deficiency, primary, type 4", "autosomal recessive spinocerebellar ataxia 9", "Autosomal recessive cerebellar ataxia type 2", "autosomal recessive cerebellar ataxia type 2", "spinocerebellar ataxia, autosomal recessive 9", "Spinocerebellar Ataxia, Autosomal Recessive 9", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 9", "Cerebellar Ataxia, Autosomal Recessive, Type 2", "autosomal recessive spinocerebellar ataxia type 9", "Autosomal recessive spinocerebellar ataxia type 9", "ARCA2 - autosomal recessive cerebellar ataxia type 2", "autosomal recessive ataxia due to ubiquinone deficiency", "Autosomal recessive ataxia due to ubiquinone deficiency", "autosomal recessive ataxia due to coenzyme Q10 deficiency", "Autosomal recessive ataxia due to coenzyme Q10 deficiency", "Autosomal recessive ataxia due to ubiquinone deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive ataxia due to ubiquinone deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0011472", "names": ["EDSFS", "McGrath syndrome", "MCGRATH SYNDROME", "Mcgrath syndrome", "Ectodermal dysplasia skin fragility syndrome", "Ectodermal Dysplasia-Skin Fragility Syndrome", "ectodermal dysplasia-skin fragility syndrome", "ectodermal dysplasia/skin fragility syndrome", "ECTODERMAL DYSPLASIA/SKIN FRAGILITY SYNDROME", "Ectodermal dysplasia-skin fragility syndrome", "ectodermal dysplasia skin fragility syndrome", "Ectodermal dysplasia- skin fragility syndrome", "Ectodermal dysplasia/ skin fragility syndrome", "ectodermal dysplasia - skin fragility syndrome", "Epidermolysis bullosa simplex due to plakophilin deficiency", "epidermolysis bullosa simplex due to plakophilin deficiency", "Epidermolysis bullosa simplex due to plakophilin deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolysis bullosa simplex due to plakophilin deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C1336442", "names": ["Stage IV Thyroid Medullary Carcinoma", "Stage IV Medullary Carcinoma of Thyroid", "Stage IV Thyroid Gland Medullary Cancer", "Stage IV Thyroid Gland Medullary Carcinoma", "Stage IV Medullary Thyroid Gland Carcinoma", "Stage IV Medullary Carcinoma of the Thyroid", "Stage IV Medullary Carcinoma of Thyroid Gland", "Stage IV Medullary Carcinoma of the Thyroid Gland", "Stage IV Thyroid Gland Medullary Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Thyroid Gland Medullary Carcinoma AJCC v7", "shortest_name_length": 36}
{"curie": "UMLS:C1519009", "names": ["Peritoneal EGIST", "Peritoneal Gastrointestinal Stromal Tumor", "Peritoneal Extragastrointestinal Stromal Tumor", "Peritoneal Gastrointestinal Stromal Tumor (GIST)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peritoneal Gastrointestinal Stromal Tumor", "shortest_name_length": 16}
{"curie": "MONDO:0001678", "names": ["intestine tuberculosis", "intestinal tuberculosis", "INTESTINAL TUBERCULOSIS", "Tuberculosis;intestinal", "tuberculosis intestinal", "Intestinal tuberculosis", "tuberculosis intestines", "Intestines--Tuberculosis", "Tuberculosis of intestine", "tuberculosis of intestine", "ENTEROCOLITIS, TUBERCULOUS", "tuberculosis of intestines", "Tuberculosis of intestines", "bowel; tuberculous (etiology)", "Tuberculosis of intestinal tract", "intestine; tuberculous (etiology)", "Tuberculous enteritis of intestine", "bowel; tuberculous (manifestation)", "Tuberculosis of intestine (disorder)", "intestine; tuberculous (manifestation)", "tuberculosis of intestines (diagnosis)", "Tuberculosis of intestines and mesenteric glands"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intestinal tuberculosis", "shortest_name_length": 22}
{"curie": "MONDO:0011463", "names": ["Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy", "polyneuropathy, lethal neonatal, axonal sensorimotor, autosomal recessive", "POLYNEUROPATHY, LETHAL NEONATAL, AXONAL SENSORIMOTOR, AUTOSOMAL RECESSIVE", "Polyneuropathy, Lethal Neonatal, Axonal Sensorimotor, Autosomal Recessive", "Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyneuropathy, lethal neonatal, axonal sensorimotor, autosomal recessive", "shortest_name_length": 70}
{"curie": "MONDO:0013175", "names": ["RP50", "Retinitis Pigmentosa 50", "RETINITIS PIGMENTOSA 50", "retinitis pigmentosa-50", "retinitis pigmentosa 50", "BEST1 retinitis pigmentosa", "retinitis pigmentosa type 50", "Retinitis Pigmentosa, Concentric", "RETINITIS PIGMENTOSA, CONCENTRIC", "retinitis pigmentosa, concentric", "RETINITIS PIGMENTOSA, CONCENTRIC (disorder)", "retinitis pigmentosa caused by mutation in BEST1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 50", "shortest_name_length": 4}
{"curie": "MONDO:0023148", "names": ["fetal phenothiazine syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fetal phenothiazine syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0008841", "names": ["ataxia-telangiectasia with generalized skin pigmentation and early death", "Ataxia-Telangiectasia with Generalized Skin Pigmentation and Early Death", "ATAXIA-TELANGIECTASIA WITH GENERALIZED SKIN PIGMENTATION AND EARLY DEATH"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ataxia-telangiectasia with generalized skin pigmentation and early death", "shortest_name_length": 72}
{"curie": "UMLS:C5205712", "names": ["Sinonasal Adenocarcinoma, Intestinal-Type with Mixed Pattern"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Adenocarcinoma, Intestinal-Type with Mixed Pattern", "shortest_name_length": 60}
{"curie": "MONDO:0018824", "names": ["Pyoderma gangenosum", "pyoderma gangrenous", "PYODERMA GANGRENOSA", "Pyoderma gangrenous", "PYODERMA GANGRENOUS", "gangrenous pyoderma", "pyoderma gangenosum", "pyoderma gangrenosa", "gangrenosum pyoderma", "Pyoderma Gangrenosum", "pyoderma gangrenosum", "Pyoderma gangrenosum", "PYODERMA GANGRENOSUM", "gangrenosum; pyoderma", "pyoderma; gangrenosum", "Pyoderma gangrenosum (disorder)", "pyoderma gangrenosum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyoderma gangrenosum", "shortest_name_length": 19}
{"curie": "UMLS:C0334602", "names": ["olfactory neurogenic tumor", "Olfactory neurogenic tumor", "Olfactory Neurogenic Tumor", "tumor; neurogenic olfactory", "neurogenic olfactory; tumor", "Olfactory neurogenic tumour", "olfactory neurogenic tumor (diagnosis)", "Olfactory neurogenic tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Olfactory neurogenic tumor", "shortest_name_length": 26}
{"curie": "MONDO:0024377", "names": ["DSPD", "DSPS", "delayed phase sleep syndrome", "Delayed sleep phase syndrome", "Delayed Sleep Phase Syndrome", "delayed sleep phase syndrome", "Delayed Sleep-Phase Syndrome", "syndrome; delayed sleep phase", "Delayed Sleep-Phase Syndromes", "delayed; sleep phase, syndrome", "Delayed sleep-wake phase disorder", "sleepwake schedule disorder, delayed phase", "sleep-wake schedule disorder, delayed phase", "Sleep-wake schedule disorder, delayed phase type", "sleep wake schedule disorder, delayed phase type", "Circadian rhythm sleep disorder, delayed sleep phase", "Delayed Sleep Phase Type Circadian Rhythm Sleep Disorder", "circadian rhythm sleep disorder, delayed sleep phase type", "Circadian rhythm sleep disorder, delayed sleep phase type", "sleep disorder circadian rhythm, delayed sleep phase type", "organic circadian rhythm sleep disorder delayed sleep phase", "Sleep-wake schedule disorder, delayed phase type (disorder)", "organic circadian rhythm sleep disorder, delayed sleep phase type", "Circadian rhythm sleep disorder, delayed sleep phase type (diagnosis)", "organic circadian rhythm sleep disorder, delayed sleep phase type (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "circadian rhythm sleep disorder, delayed sleep phase type", "shortest_name_length": 4}
{"curie": "MONDO:0021119", "names": ["nonfunctioning tumor", "endocrine-inactive tumor", "nonfunctional Endocrine neoplasm", "Nonfunctional Endocrine Neoplasm", "Nonfunctioning Endocrine Neoplasm", "non-functioning endocrine neoplasm", "Non-Functioning Endocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-functioning endocrine neoplasm", "shortest_name_length": 20}
{"curie": "MONDO:0014906", "names": ["CMT2A2B", "AR-CMT2, Ouvrier type", "SEOAN due to MFN2 deficiency", "Charcot-Marie-Tooth disease type 2A2B", "Charcot-Marie-Tooth Disease Type 2A2B", "Charcot-Marie-Tooth disease, axonal, type 2A2B", "severe early-onset axonal neuropathy due to MFN2 deficiency", "autosomal recessive Charcot-Marie-Tooth disease, Ouvrier type", "Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2A2B", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2A2B", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2B, AUTOSOMAL RECESSIVE", "Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2a2b;"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2a2b;", "shortest_name_length": 7}
{"curie": "MONDO:0100408", "names": ["AML, t(16;21)(q24;q22)", "acute myeloid leukemia, t(16;21)(q24;q22)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, t(16;21)(q24;q22)", "shortest_name_length": 22}
{"curie": "MONDO:0015533", "names": ["benign cephalic histiocytosis", "Benign cephalic histiocytosis", "Papular histiocytosis of head", "Benign cephalic histiocytosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign cephalic histiocytosis", "shortest_name_length": 29}
{"curie": "MONDO:0020115", "names": ["Acquired polycythemia", "secondary; erythremia", "acquired polycythemia", "erythremia; secondary", "Secondary Polycythemia", "Polycythemia, acquired", "secondary polycythemia", "SECONDARY POLYCYTHEMIA", "Acquired polycythaemia", "polycythemia secondary", "Secondary polycythemia", "acquired; polycythemia", "polycythemia; acquired", "POLYCYTHEMIA, SECONDARY", "SECONDARY POLYCYTHEMIAS", "secondary polycythaemia", "Secondary polycythaemia", "Polycythaemia;secondary", "secondary; polycythemia", "Polycythemia, secondary", "polycythemia; secondary", "Secondary erythrocytosis", "secondary erythrocytosis", "Polycythaemia, secondary", "Erythrocytosis, secondary", "Acquired polycythemia, NOS", "Secondary polycythemia, NOS", "Acquired polycythaemia, NOS", "Secondary polycythaemia, NOS", "Secondary erythrocytosis, NOS", "secondary polycythemia acquired", "Acquired secondary polycythemia", "Secondary polycythemia (disorder)", "Acquired secondary erythrocytosis", "acquired polycythemia (diagnosis)", "secondary polycythemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary polycythemia", "shortest_name_length": 21}
{"curie": "MONDO:0100473", "names": ["disorder of peptide and amine metabolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of peptide and amine metabolism", "shortest_name_length": 40}
{"curie": "MONDO:0005057", "names": ["LCNEC", "Large Cell NEC", "large cell NEC", "Large Cell Neuroendocrine Carcinoma", "large-cell neuroendocrine carcinoma", "large cell neuroendocrine carcinoma", "Large-cell neuroendocrine carcinoma", "Large cell neuroendocrine carcinoma", "large cell neuroendocrine carcinoma (diagnosis)", "Large cell neuroendocrine carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "large cell neuroendocrine carcinoma", "shortest_name_length": 5}
{"curie": "MONDO:0016037", "names": ["superficial Fibromatosis", "Superficial Fibromatosis", "Superficial fibromatosis", "Superficial fibromatosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "superficial Fibromatosis", "shortest_name_length": 24}
{"curie": "UMLS:C2675370", "names": ["Capillary Malformation Without Arteriovenous Malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Capillary Malformation Without Arteriovenous Malformation", "shortest_name_length": 57}
{"curie": "UMLS:C5419822", "names": ["Gallbladder Neuroendocrine Tumor G3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gallbladder Neuroendocrine Tumor G3", "shortest_name_length": 35}
{"curie": "UMLS:C5446611", "names": ["Advanced Malignant Digestive System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Malignant Digestive System Neoplasm", "shortest_name_length": 44}
{"curie": "MONDO:0002741", "names": ["Broad Ligament Adenocarcinoma", "uterine ligament adenocarcinoma", "adenocarcinoma of uterine ligament", "adenocarcinoma of uterine ligament (diagnosis)", "uterine ligament neoplasm malignant adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine ligament adenocarcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0008002", "names": ["MRMV1", "bimanual synergia", "BIMANUAL SYNERGIA", "mirror movements 1", "MIRROR MOVEMENTS 1", "mirror movements type 1", "mirror movements, congenital", "MIRROR MOVEMENTS, CONGENITAL", "DCC familial congenital mirror movements", "mirror movements 1 and/Or agenesis of the corpus callosum", "MIRROR MOVEMENTS 1 AND/OR AGENESIS OF THE CORPUS CALLOSUM", "familial congenital mirror movements caused by mutation in DCC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mirror movements 1", "shortest_name_length": 5}
{"curie": "MONDO:0019424", "names": ["X-linked intellectual disability-acromegaly-hyperactivity syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability-acromegaly-hyperactivity syndrome", "shortest_name_length": 66}
{"curie": "MONDO:0009212", "names": ["F10 deficiency", "factor X deficiency", "factor 10 deficiency", "disease, Stuart-Prower", "Hereditary Factor X Deficiency", "hereditary Factor X deficiency", "congenital factor X deficiency", "Stuart-Prower Factor deficiency", "Stuart-Prower factor deficiency", "Stuart-Prower Factor Deficiency", "factor X deficiency, congenital", "congenital Stuart factor deficiency", "Stuart factor deficiency, congenital", "Hereditary factor X deficiency disease", "congenital factor X deficiency (diagnosis)", "Hereditary Stuart-Prower deficiency disease", "Hereditary Stuart factor deficiency disease", "Hereditary factor X deficiency disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital factor X deficiency", "shortest_name_length": 14}
{"curie": "MONDO:0013560", "names": ["HPS8", "HERMANSKY-PUDLAK SYNDROME 8", "Hermansky-Pudlak syndrome 8", "Hermansky-Pudlak syndrome type 8", "BLOC1S3 Hermansky-Pudlak syndrome", "Hermansky-Pudlak syndrome caused by mutation in BLOC1S3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hermansky-Pudlak syndrome 8", "shortest_name_length": 4}
{"curie": "MONDO:0044320", "names": ["RP79", "retinitis pigmentosa 79", "RETINITIS PIGMENTOSA 79"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 79", "shortest_name_length": 4}
{"curie": "UMLS:C4682572", "names": ["Stage IIIA Uterine Corpus Endometrial Stromal Sarcoma", "Stage IIIA Uterine Corpus Endometrial Stromal Sarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Uterine Corpus Endometrial Stromal Sarcoma AJCC v8", "shortest_name_length": 53}
{"curie": "UMLS:C1275975", "names": ["Skin Myxofibrosarcoma", "Dermal Myxofibrosarcoma", "Myxofibrosarcoma of skin", "soft tissue myxofibrosarcoma", "Myxofibrosarcoma of skin (disorder)", "Myxofibrosarcoma of skin (diagnosis)", "Myxoid malignant fibrous histiocytoma of skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myxofibrosarcoma of skin", "shortest_name_length": 21}
{"curie": "UMLS:C4763993", "names": ["Venomous Animal Contact"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Venomous Animal Contact", "shortest_name_length": 23}
{"curie": "MONDO:0013546", "names": ["MC5DN2", "TMEM70 defect", "3-MGCA type IV (3-MGCA-4) (formerly)", "TMEM70 related mitochondrial encephalo-cardio-myopathy", "TMEM70-related mitochondrial encephalo-cardio-myopathy", "mitochondrial Complex 5 (ATP synthase) deficiency, Tmem70 type", "MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, TMEM70 TYPE", "mitochondrial complex V (ATP synthase) deficiency nuclear type 2", "mitochondrial Complex 5 (ATP synthase) deficiency, nuclear type 2", "mitochondrial complex V (ATP synthase) deficiency, nuclear type 2", "MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2", "Mitochondrial encephalo-cardio-myopathy due to F1Fo ATPase deficiency", "mitochondrial encephalo-cardio-myopathy due to F1Fo ATPase deficiency", "neonatal mitochondrial encephalocardiomyopathy due to ATP synthase deficiency", "Mitochondrial encephalocardiomyopathy due to transmembrane protein 70 mutation", "Mitochondrial encephalo-cardio-myopathy due to isolated ATP synthase deficiency", "mitochondrial encephalo-cardio-myopathy due to isolated ATP synthase deficiency", "Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency", "encephalocardiomyopathy, mitochondrial, neonatal, due to ATP synthase deficiency", "ENCEPHALOCARDIOMYOPATHY, MITOCHONDRIAL, NEONATAL, DUE TO ATP SYNTHASE DEFICIENCY", "Mitochondrial encephalocardiomyopathy due to transmembrane protein 70 mutation (disorder)", "Mitochondrial encephalo-cardio-myopathy due to isolated mitochondrial respiratory chain complex V deficiency", "mitochondrial encephalo-cardio-myopathy due to isolated mitochondrial respiratory chain complex V deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex V (ATP synthase) deficiency nuclear type 2", "shortest_name_length": 6}
{"curie": "MONDO:0032629", "names": ["MC1DN25", "nuclear type mitochondrial complex I deficiency 25", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 25", "mitochondrial complex 1 deficiency, nuclear type 25"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 25", "shortest_name_length": 7}
{"curie": "MONDO:0001115", "names": ["primary polycythemia", "Familial Polycythemia", "familial polycythemia", "Familiar Polycythemia", "familial erythrocytosis", "Familial Erythrocytosis", "erythrocytosis, familial", "hereditary polycythemia (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial polycythemia", "shortest_name_length": 20}
{"curie": "MONDO:0030876", "names": ["CAFD1", "CARDIOACROFACIAL DYSPLASIA 1", "cardioacrofacial dysplasia 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardioacrofacial dysplasia 1", "shortest_name_length": 5}
{"curie": "MONDO:0017117", "names": ["Congenital obstructive hydrocephalus", "congenital obstructive hydrocephalus", "congenital non-communicating hydrocephalus", "Congenital non-communicating hydrocephalus", "Congenital obstructive hydrocephalus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital non-communicating hydrocephalus", "shortest_name_length": 36}
{"curie": "MONDO:0004289", "names": ["Glottic verrucous carcinoma", "Glottic Verrucous Carcinoma", "Glottis Verrucous Carcinoma", "glottis verrucous carcinoma", "glottic verrucous carcinoma", "Verrucous Carcinoma of Glottis", "verrucous carcinoma of glottis", "Verrucous Carcinoma of the Glottis", "verrucous carcinoma of the glottis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glottis verrucous carcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C5419076", "names": ["Locally Advanced Non-Cutaneous Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Non-Cutaneous Melanoma", "shortest_name_length": 39}
{"curie": "UMLS:C2981371", "names": ["Stage IB Esophageal Adenocarcinoma", "Stage IB Esophageal Adenocarcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Esophageal Adenocarcinoma AJCC v7", "shortest_name_length": 34}
{"curie": "UMLS:C0085397", "names": ["Pasteurellaceae Infection", "Infection, Pasteurellaceae", "Pasteurellaceae Infections", "Infections, Pasteurellaceae"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pasteurellaceae Infections", "shortest_name_length": 25}
{"curie": "MONDO:0000153", "names": ["TGV", "TGA", "Complete transposition", "complete transposition", "TRANSPOSITION GREAT VESSEL", "great transposition vessel", "artery great transposition", "great vessels transposition", "great transposition vessels", "Great Vessels Transposition", "transposition great vessels", "Transposition;great vessels", "arteris great transposition", "arteries great transposition", "great vessels; transposition", "transposition; great vessels", "Great Arteries Transposition", "transposition great arteries", "Great Vessels Transpositions", "transposition of great artery", "transposition of great vessel", "Great Arteries Transpositions", "transposition of great vessels", "Transposition of Great Vessels", "Transposition of great vessels", "TRANSPOSITION OF GREAT VESSELS", "Transposition of great arteries", "transposition of great arteries", "Transposition of Great Arteries", "Total great vessel transposition", "Aorta-pulmonary art transposition", "AORTA-PULMONARY ART TRANSPOSITION", "Transposition of the great vessels", "Transposition of the Great Vessels", "transposition of the great vessels", "transposition of the great arteries", "TRANSPOSITION OF THE GREAT ARTERIES", "Transposition of the great arteries", "Transposition of great vessels, NOS", "TRANSPOSITION AORTA-PULMONARY ARTERY", "TGV - Transposition of great vessels", "Transposition aorta-pulmonary artery", "TGA - Transposition of great arteries", "Aorta-pulmonary arterial transposition", "TRANSPOSITION, GREAT VESSELS, COMPLETE", "Complete transposition of great vessels", "complete transposition of great vessels", "Classical transposition of great vessels", "complete transposition of great arteries", "Discordant ventriculoarterial connection", "Complete transposition of great arteries", "Discordant Ventriculoarterial Connection", "Transposition of great vessels (complete)", "Transposition of great vessels, classical", "Transposition of the great arteries (TGA)", "Dextro-looped transposition of the great arteries", "Complete transposition of great vessels (disorder)", "complete transposition of great vessels (diagnosis)", "Discordant ventriculoarterial connection (disorder)", "complete transposition of great arteries (diagnosis)", "Discordant ventriculoarterial connection with concordant atrioventricular connection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transposition of the great arteries", "shortest_name_length": 3}
{"curie": "MONDO:0010768", "names": ["GBY", "Gonocytoma", "gonadoblastoma", "gonad blastoma", "Gonadoblastoma", "GONADOBLASTOMA", "gonadoblastomas", "Gonadoblastomas", "GBY - Gonadoblastoma", "Gonadoblastoma (disorder)", "Gonadoblastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gonadoblastoma", "shortest_name_length": 3}
{"curie": "MONDO:0006578", "names": ["mediastinal lipomatosis", "Mediastinal Lipomatosis", "mediastinal lipomatosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mediastinal lipomatosis", "shortest_name_length": 23}
{"curie": "UMLS:C0751074", "names": ["Diabetic Neuralgia", "diabetic neuralgia", "Neuralgia, Diabetic", "Diabetic Neuralgias", "Neuralgias, Diabetic", "painful diabetic neuropathy", "Painful Diabetic Neuropathy", "Neuropathy, Painful Diabetic", "Diabetic Neuropathy, Painful", "Painful Diabetic Neuropathies", "Diabetic Neuropathies, Painful", "Neuropathies, Painful Diabetic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diabetic Neuralgia", "shortest_name_length": 18}
{"curie": "MONDO:0034976", "names": ["iatrogenic Creutzfeldt-Jakob disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "iatrogenic Creutzfeldt-Jakob disease", "shortest_name_length": 36}
{"curie": "UMLS:C4524967", "names": ["stage IIIA small intestine cancer", "Stage IIIA Small Intestinal Adenocarcinoma", "stage IIIA small intestinal adenocarcinoma AJCC v8", "Stage IIIA Small Intestinal Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Small Intestinal Adenocarcinoma AJCC v8", "shortest_name_length": 33}
{"curie": "MONDO:0021637", "names": ["LGG", "benign glioma", "Low grade glioma", "low grade glioma", "Low Grade Glioma", "low-grade glioma", "Low-Grade Glioma", "Low-grade glioma", "CNS, low grade glioma (LGG)", "Low grade glioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "low grade glioma", "shortest_name_length": 3}
{"curie": "UMLS:C1334559", "names": ["Malignant Anterior Tongue Tumor", "Malignant Anterior Tongue Neoplasm", "Malignant Tumor of Anterior Tongue", "Malignant Neoplasm of Anterior Tongue", "Malignant Tumor of the Anterior Tongue", "Malignant Neoplasm of the Anterior Tongue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Anterior Tongue Neoplasm", "shortest_name_length": 31}
{"curie": "MONDO:0011949", "names": ["Thai Symphalangism Syndrome", "THAI SYMPHALANGISM SYNDROME", "Thai symphalangism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thai symphalangism syndrome", "shortest_name_length": 27}
{"curie": "MONDO:0015947", "names": ["fish-skin", "fish skin", "Fish skin", "ichthyosis", "Ichthyosis", "Fish skin, NOS", "Fish scale disease", "genetic ichthyosis", "fish scale disease", "inherited ichthyosis", "ICHTHYOSIS CONGENITA", "ichthyosis congenita", "Ichthyosis Congenita", "Ichthyosis congenita", "ichthyosis congenital", "congenital ichthyosis", "Congenital ichthyosis", "Ichthyosis congenital", "inherited genetic ichthyosis", "Newborn Lamellar Exfoliation", "Newborn Lamellar Exfoliations", "Congenital ichthyosis of skin", "congenital ichthyosis of skin", "hereditary ichthyosis (disease)", "Lamellar Exfoliation of Newborn", "LAMELLAR EXFOLIATION OF NEWBORN", "disease (or disorder); fish-skin", "congenital ichthyosis (diagnosis)", "Congenital ichthyosis of skin, NOS", "Congenital ichthyosis, unspecified", "Congenital ichthyosis of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited ichthyosis", "shortest_name_length": 9}
{"curie": "MONDO:0018674", "names": ["Kuttner tumor", "Kuttner Tumor", "Küttner tumor", "Kuttner's Tumor", "Kuttner's tumor", "IgG4-related sialadenitis", "Chronic sclerosing sialadenitis", "chronic sclerosing sialadenitis", "Chronic Sclerosing Sialadenitis", "IgG4-related submandibular gland disease", "Chronic sclerosing sialadenitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IgG4-related submandibular gland disease", "shortest_name_length": 13}
{"curie": "UMLS:C0751177", "names": ["Head Cancer", "head cancer", "cancer head", "Head Cancers", "Head--Cancer", "Cancer, Head", "cancers head", "Cancers, Head", "Cancer of Head", "of head cancer", "cancer of the head", "Cancer of the Head", "malignant neoplasm of head", "Malignant neoplasm of head, NOS", "malignant neoplasm of head (diagnosis)", "malignant neoplasm of ill-defined site head"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cancer of Head", "shortest_name_length": 11}
{"curie": "MONDO:0025420", "names": ["TGE", "swine transmissible gastroenteritis", "Swine Transmissible Gastroenteritis", "Gastroenteritis, Swine Transmissible", "gastroenteritis, swine transmissible", "transmissible gastroenteritis, swine", "Transmissible Gastroenteritis, Swine", "swine transmissible Gastroenteritides", "transmissible porcine gastroenteritis", "Porcine Transmissible Gastroenteritis", "porcine transmissible gastroenteritis", "Transmissible Porcine Gastroenteritis", "Swine Transmissible Gastroenteritides", "gastroenteritis, porcine transmissible", "Transmissible Gastroenteritis, Porcine", "Transmissible Gastroenteritides, Swine", "gastroenteritis, transmissible porcine", "transmissible gastroenteritis, porcine", "Gastroenteritides, Swine Transmissible", "Gastroenteritis, Porcine Transmissible", "Gastroenteritis, Transmissible Porcine", "porcine gastroenteritis, transmissible", "Porcine Gastroenteritis, Transmissible", "transmissible Gastroenteritides, swine", "Transmissible Gastroenteritis of Swine", "Transmissible gastroenteritis of swine", "transmissible gastroenteritis of swine", "Gastroenteritides, swine transmissible", "Transmissible Porcine Gastroenteritides", "gastroenteritis, transmissible, porcine", "Gastroenteritis, Transmissible, Porcine", "porcine transmissible Gastroenteritides", "transmissible porcine Gastroenteritides", "Porcine Transmissible Gastroenteritides", "Gastroenteritis, Transmissible, of Swine", "Transmissible Gastroenteritides, Porcine", "gastroenteritis, transmissible, of swine", "Gastroenteritides, Transmissible Porcine", "Gastroenteritides, Porcine Transmissible", "Porcine Gastroenteritides, Transmissible", "porcine Gastroenteritides, transmissible", "Gastroenteritides, transmissible porcine", "Gastroenteritides, porcine transmissible", "transmissible Gastroenteritides, porcine", "Transmissible gastroenteritis of swine (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastroenteritis, transmissible, of swine", "shortest_name_length": 3}
{"curie": "MONDO:0004028", "names": ["small bowel fibrosarcoma", "Small Bowel Fibrosarcoma", "fibrosarcoma of small bowel", "Fibrosarcoma of Small Bowel", "small intestine fibrosarcoma", "Small Intestine Fibrosarcoma", "small intestinal fibrosarcoma", "Small Intestinal Fibrosarcoma", "Fibrosarcoma, small Intestine", "Fibrosarcoma, Small Intestine", "fibrosarcoma, small intestine", "fibrosarcoma of the small bowel", "fibrosarcoma of small intestine", "Fibrosarcoma of the Small Bowel", "Fibrosarcoma of Small Intestine", "fibrosarcoma of the small intestine", "Fibrosarcoma of the Small Intestine", "small intestine fibrosarcoma (disease)", "fibrosarcoma of small intestine (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small intestinal fibrosarcoma", "shortest_name_length": 24}
{"curie": "MONDO:0006968", "names": ["Shoulder Impingement", "Impingement, Shoulder", "Shoulder Impingements", "Subacromial impingement", "subacromial impingement", "Rotator Cuff Impingement", "Impingement, Rotator Cuff", "Rotator Cuff Impingements", "Impingements, Rotator Cuff", "Shoulder Impingement Syndrome", "impingement syndrome shoulder", "Shoulder impingement syndrome", "shoulder impingement syndrome", "shoulder syndrome impingement", "Impingement syndrome shoulder", "Shoulder Impingement Syndromes", "subacromial impingement syndrome", "Impingement syndrome of shoulder", "Rotator Cuff Impingement Syndrome", "Subacromial impingement (disorder)", "subacromial impingement (diagnosis)", "Impingement syndrome of shoulder region", "Impingement syndrome of shoulder region (disorder)", "shoulder impingement syndrome (disorder) [ambiguous]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "shoulder impingement syndrome", "shortest_name_length": 20}
{"curie": "MONDO:0017203", "names": ["chronic endophthalmitis", "Chronic endophthalmitis", "endophthalmitis, chronic", "Chronic endophthalmitis (disorder)", "chronic endophthalmitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic endophthalmitis", "shortest_name_length": 23}
{"curie": "MONDO:0006685", "names": ["Brain Hypoxia Ischemia", "Brain Ischemia Hypoxia", "Brain Ischemia-Hypoxia", "Brain Hypoxia-Ischemia", "Brain Hypoxia-Ischemias", "Ischemia-Hypoxia, Brain", "Hypoxia-Ischemia, Brain", "Hypoxia Ischemia, Brain", "Ischemia Hypoxia, Brain", "Brain Ischemia-Hypoxias", "brain hypoxia - ischemia", "Hypoxia-Ischemias, Brain", "Ischemia-Hypoxias, Brain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brain hypoxia - ischemia", "shortest_name_length": 22}
{"curie": "MONDO:0030696", "names": ["MTDPS20", "mitochondrial DNA depletion syndrome 20", "mitochondrial DNA depletion syndrome 20 (mngie type)", "MITOCHONDRIAL DNA DEPLETION SYNDROME 20 (MNGIE TYPE)", "mitochondrial DNA depletion syndrome 20 (MNGIE type)", "mitochondrial neurogastrointestinal encephalomyopathy syndrome, lig3-related", "MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOMYOPATHY SYNDROME, LIG3-RELATED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial DNA depletion syndrome 20 (mngie type)", "shortest_name_length": 7}
{"curie": "UMLS:C5668296", "names": ["Metastatic Malignant Abdominal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Malignant Abdominal Neoplasm", "shortest_name_length": 39}
{"curie": "MONDO:0018617", "names": ["baroreflex failure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "baroreflex failure", "shortest_name_length": 18}
{"curie": "UMLS:C3897756", "names": ["Recurrent Diffuse Astrocytoma", "recurrent childhood diffuse astrocytoma", "Recurrent Childhood Diffuse Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Diffuse Astrocytoma", "shortest_name_length": 29}
{"curie": "MONDO:0015049", "names": ["Hepatic solitary necrotic nodule", "hepatic solitary necrotic nodule", "Solitary necrotic nodule of liver", "solitary necrotic nodule of the liver", "Solitary necrotic nodule of the liver", "Solitary necrotic nodule of liver (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "solitary necrotic nodule of the liver", "shortest_name_length": 32}
{"curie": "MONDO:0027676", "names": ["MCRD", "PUJO", "UPJO", "CAKUT2", "Bilateral MCDK", "Ureteropelvic obstruction", "Pelviureteric obstruction", "Pelvi-ureteric obstruction", "HYDRONEPHROSIS DUE TO PUJO", "hydronephrosis due to Pujo", "Hydronephrosis Due To Pujo", "Ureteropelvic junction stenosis", "PUJ - Pelviureteric obstruction", "UPJ - Ureteropelvic obstruction", "PUO - Pelviureteric obstruction", "stenosis; ureteropelvic junction", "ureteropelvic junction; stenosis", "ureteropelvic junction; stricture", "stricture; ureteropelvic junction", "Pelviureteric Junction Obstruction", "Ureteropelvic Junction Obstruction", "URETEROPELVIC JUNCTION OBSTRUCTION", "Pelviureteric junction obstruction", "PELVIURETERIC JUNCTION OBSTRUCTION", "pelviureteric junction obstruction", "Ureteropelvic junction obstruction", "ureteropelvic junction obstruction", "Pelvi-ureteric junction obstruction", "obstruction; ureteropelvic junction", "ureteropelvic junction; obstruction", "Bilateral multicystic renal dysplasia", "Obstruction of pelviureteric junction", "Obstruction of Pelviureteric Junction", "Multicystic renal dysplasia, bilateral", "MULTICYSTIC RENAL DYSPLASIA, BILATERAL", "Ureteropelvic junction obstruction NOS", "multicystic renal dysplasia, bilateral", "Bilateral multicystic dysplastic kidney", "Obstruction of pelviureteric junction (disorder)", "Bilateral multicystic renal dysplasia (disorder)", "congenital anomalies of kidney and urinary tract 2", "CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 2", "TBX18 congenital anomaly of kidney and urinary tract", "Congenital anomalies of the kidney and urinary tract 2", "congenital anomalies of kidney and urinary tract type 2", "congenital anomaly of kidney and urinary tract caused by mutation in TBX18"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital anomalies of kidney and urinary tract 2", "shortest_name_length": 4}
{"curie": "MONDO:0016553", "names": ["isolated congenital hypogonadotropic hypogonadism", "nonsyndromic congenital hypogonadotropic hypogonadism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated congenital hypogonadotropic hypogonadism", "shortest_name_length": 49}
{"curie": "MONDO:0018207", "names": ["Del(2)(p13.2)", "2p13.2 microdeletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "2p13.2 microdeletion syndrome", "shortest_name_length": 13}
{"curie": "UMLS:C3889038", "names": ["Nr-axSpA", "Non Radiographic Axial Spondyloarthritis", "Non-Radiographic Axial Spondyloarthritis", "Non-radiographic axial spondyloarthritis", "Spondyloarthritis, Non-Radiographic Axial", "Axial Spondyloarthritis, Non-Radiographic", "Non-Radiographic Axial Spondyloarthritides", "nr-axSpA - non-radiographic axial spondylitis", "ankylosing spondylitis non-radiographic axial", "Non-radiographic axial spondyloarthritis (disorder)", "Non-radiographic axial spondyloarthritis (diagnosis)", "Axial spondyloarthritis without radiographic evidence of ankylosing spondylitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Radiographic Axial Spondyloarthritis", "shortest_name_length": 8}
{"curie": "UMLS:C1142397", "names": ["myoglobinemia", "Myoglobinemia", "myoglobinaemia", "Myoglobinaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myoglobinaemia", "shortest_name_length": 13}
{"curie": "MONDO:0011698", "names": ["GNMT deficiency", "GNMT Deficiency", "GNMT DEFICIENCY", "Glycine N-Methyltransferase Deficiency", "GLYCINE N-METHYLTRANSFERASE DEFICIENCY", "glycine N-methyltransferase deficiency", "Glycine N-methyltransferase deficiency", "Hypermethioninemia due to GNMT deficiency", "hypermethioninemia due to GNMT deficiency", "Hypermethioninemia due to glycine N-methyltransferase deficiency", "hypermethioninemia due to glycine N-methyltransferase deficiency", "Hypermethioninemia due to deficiency of glycine N-methyltransferase", "hypermethioninemia due to deficiency of glycine n-methyltransferase", "Hypermethioninaemia due to deficiency of glycine N-methyltransferase", "Hypermethioninemia due to GNMT (glycine N-methyltransferase) deficiency", "Hypermethioninaemia due to GNMT (glycine N-methyltransferase) deficiency", "Hypermethioninemia due to deficiency of glycine N-methyltransferase (disorder)", "hypermethioninemia due to deficiency of glycine n-methyltransferase (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycine N-methyltransferase deficiency", "shortest_name_length": 15}
{"curie": "MONDO:0008854", "names": ["BBS1", "BARDET-BIEDL SYNDROME 1", "Bardet-Biedl syndrome 1", "Bardet-Biedl syndrome type 1", "Bardet-Biedl syndrome 1, modifier of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bardet-Biedl syndrome 1", "shortest_name_length": 4}
{"curie": "UMLS:C0271175", "names": ["Cataract radiation", "Radiation cataract", "radiation cataract", "cataract radiation", "cataract; radiation", "radiation; cataract", "cataracts radiation", "irradiation; cataract", "cataract; irradiation", "Radiation-induced cataract", "radiation-induced cataract", "Radiation-Induced Cataract", "Cataract associated with radiation", "radiation-induced cataract (diagnosis)", "Cataract associated with radiation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cataract associated with radiation", "shortest_name_length": 18}
{"curie": "MONDO:0011272", "names": ["RP25", "RP 25", "retinitis pigmentosa 25", "RETINITIS PIGMENTOSA 25", "Retinitis Pigmentosa 25", "EYS retinitis pigmentosa", "retinitis pigmentosa type 25", "retinitis pigmentosa caused by mutation in EYS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 25", "shortest_name_length": 4}
{"curie": "UMLS:C0268821", "names": ["Urinary tract infect;lower", "lower urinary tract infection", "Lower urinary tract infection", "urinary tract infection, lower", "UTI - Lower urinary tract infection", "urinary tract lower infectious disease", "Lower urinary tract infectious disease", "Lower urinary tract infectious disease, NOS", "Lower urinary tract infectious disease (disorder)", "Lower urinary tract infectious disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lower urinary tract infectious disease", "shortest_name_length": 26}
{"curie": "MONDO:0020399", "names": ["Hypoplasia of mitral valve annulus", "Hypoplasia of the mitral valve annulus", "Hypoplasia of mitral valve annulus (disorder)", "Hypoplasia of mitral valve annulus (diagnosis)", "congenital hypoplasia of the mitral valve annulus", "mitral valve disorder congenital hypoplasia annulus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital hypoplasia of the mitral valve annulus", "shortest_name_length": 34}
{"curie": "UMLS:C4521491", "names": ["Stage III Liver Cancer", "Stage IIIC Adult Liver Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Adult Liver Cancer AJCC v7", "shortest_name_length": 22}
{"curie": "MONDO:0018850", "names": ["Pilar cyst", "Pilar Cyst", "pilar tumor", "Pilar Tumor", "Pilar tumor", "Pilar tumour", "pilar tumors", "proliferating pilar cyst", "Proliferating pilar cyst", "Proliferating Pilar Tumor", "proliferating Pilar tumor", "Proliferating Trichilemmal Cyst", "proliferating trichilemmal cyst", "Proliferating trichilemmal cyst", "Trichilemmal proliferating cyst", "trichilemmal proliferating cyst", "Proliferating tricholemmal cyst", "proliferating pilar cystic tumor", "Proliferating trichilemmal tumor", "proliferating Tricholemmal tumor", "proliferating trichilemmal tumor", "Proliferating Trichilemmal Tumor", "Proliferating Tricholemmal Tumor", "Trichilemmal (proliferating) cyst", "Proliferating trichilemmal tumour", "Proliferating pilar cyst (disorder)", "Pilar tumor (morphologic abnormality)", "trichilemmal proliferating cyst (diagnosis)", "Proliferating trichilemmal tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "proliferating trichilemmal cyst", "shortest_name_length": 10}
{"curie": "MONDO:0033364", "names": ["DEE55", "EIEE55", "GPIBD14", "infantile epileptic encephalopathy 55", "early infantile epileptic encephalopathy 55", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 55", "epileptic encephalopathy, early infantile, 55", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 55", "developmental and epileptic encephalopathy 55", "developmental and epileptic encephalopathy, 55", "GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 14", "glycosylphosphatidylinositol biosynthesis defect 14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 55", "shortest_name_length": 5}
{"curie": "MONDO:0009082", "names": ["DFNMYP", "deafness and myopia", "DEAFNESS AND MYOPIA", "Deafness and myopia syndrome", "deafness and myopia syndrome", "High myopia and sensorineural deafness", "Deafness and myopia syndrome (disorder)", "high myopia-sensorineural deafness syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "high myopia-sensorineural deafness syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C5446471", "names": ["Locally Recurrent Anal Canal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Recurrent Anal Canal Squamous Cell Carcinoma", "shortest_name_length": 52}
{"curie": "MONDO:0033309", "names": ["JBTS32", "JOUBERT SYNDROME 32", "Joubert syndrome 32"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome 32", "shortest_name_length": 6}
{"curie": "UMLS:C5420391", "names": ["Non-Neoplastic Appendix Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Appendix Disorder", "shortest_name_length": 32}
{"curie": "UMLS:C1298714", "names": ["Congenital ureteropelvic junction stenosis", "Congenital pelviureteric junction obstruction", "Congenital Ureteropelvic Junction Obstruction", "Congenital ureteropelvic junction obstruction", "obstruction; ureteropelvic junction, congenital", "ureteropelvic junction; obstruction, congenital", "Congenital obstruction of ureteropelvic junction", "congenital obstruction of ureteropelvic junction", "Congenital obstruction of ureteropelvic junction (disorder)", "congenital obstruction of ureteropelvic junction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital obstruction of ureteropelvic junction", "shortest_name_length": 42}
{"curie": "MONDO:0100425", "names": ["AML, KRAS gene mutation", "AML, KRAS Gene Mutation", "AML, KRAS2 Gene Mutation", "AML, KRAS-2 Gene Mutation", "AML, c-K-ras Gene Mutation", "acute myeloid leukemia, KRAS gene mutation", "AML, v-Ki-ras2 Kirsten Rat Sarcoma Viral Oncogene Homolog Gene Mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, KRAS gene mutation", "shortest_name_length": 23}
{"curie": "MONDO:0054549", "names": ["PBD10B", "PEROXISOME BIOGENESIS DISORDER 10B", "peroxisome biogenesis disorder 10B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder 10B", "shortest_name_length": 6}
{"curie": "MONDO:0018137", "names": ["OCA1TS", "OCA1-TS", "TS OCA type 1", "Temperature-sensitive oculocutaneous albinism type 1", "temperature-sensitive oculocutaneous albinism type 1", "ALBINISM, OCULOCUTANEOUS TYPE I, TEMPERATURE-SENSITIVE", "Albinism, Oculocutaneous, Type I, Temperature-Sensitive", "ALBINISM, OCULOCUTANEOUS, TYPE I, TEMPERATURE-SENSITIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "temperature-sensitive oculocutaneous albinism type 1", "shortest_name_length": 6}
{"curie": "MONDO:0004319", "names": ["SCCOHT", "hypercalcemic type ovarian small cell carcinoma", "ovarian small cell carcinoma, hypercalcemic type", "Ovarian Small Cell Carcinoma, Hypercalcemic Type", "small-cell carcinoma of the ovary of hypercalcemic type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypercalcemic type ovarian small cell carcinoma", "shortest_name_length": 6}
{"curie": "MONDO:0007745", "names": ["HBLRG", "Gilbert", "Gilbert disease", "GILBERT DISEASE", "gilbert disease", "Gilbert Disease", "GILBERT SYNDROME", "Gilbert syndrome", "gilberts disease", "Gilbert Syndrome", "diseases gilbert", "Gilberts disease", "Gilberts Disease", "gilbert syndrome", "Disease;Gilberts", "Disease, Gilbert", "GILBERT'S DISEASE", "Gilberts syndrome", "gilbert syndromes", "familial cholemia", "cholemia; Gilbert", "gilbert's disease", "Gilbert's Disease", "Gilbert; cholemia", "Syndrome, Gilbert", "GILBERTS SYNDROME", "Gilbert's disease", "Gilberts Syndrome", "gilberts syndrome", "Gilbert's Syndrome", "gilbert's syndrome", "Gilbert's syndrome", "familial; cholemia", "Disease, Gilbert's", "syndrome gilbert's", "cholemia; familial", "Syndrome, Gilbert's", "Hyperbilirubinemia 1", "Hyperbilirubinemia I", "hyperbilirubinemia 1", "HYPERBILIRUBINEMIA I", "meulengracht syndrome", "Meulengracht syndrome", "Hyperbilirubinemia 1s", "Meulengracht Syndrome", "hyperbilirubinemia type 1", "Gilbert Disease (disorder)", "Cholemia familiaris simplex", "Gilbert-Lereboullet Syndrome", "GILBERT-LEREBOULLET SYNDROME", "Congenital familial cholemia", "Cholaemia familiaris simplex", "Gilbert-Lereboullet syndrome", "Arias Type Hyperbilirubinemia", "Gilbert-Meulengracht syndrome", "Gilbert's syndrome (disorder)", "Congenital familial cholaemia", "HYPERBILIRUBINEMIA, ARIAS TYPE", "Arias Type Hyperbilirubinemias", "Familial nonhemolytic jaundice", "Gilbert's syndrome (diagnosis)", "hyperbilirubinemia, Arias type", "Familial Nonhemolytic Jaundice", "Hyperbilirubinemia, Arias Type", "familial nonhemolytic jaundice", "Hyperbilirubinemias, Arias Type", "Familial nonhaemolytic jaundice", "Familial non-hemolytic jaundice", "familial; nonhemolytic jaundice", "jaundice; familial nonhemolytic", "hereditary nonhemolytic jaundice", "HYPERBILIRUBINEMIA, GILBERT TYPE", "congenital nonhemolytic jaundice", "familial; jaundice, nonhemolytic", "hyperbilirubinemia, Gilbert type", "Hereditary nonhemolytic jaundice", "Constitutional Liver Dysfunction", "Unconjugated Benign Bilirubinemia", "Jaundice, congenital nonhemolytic", "Hereditary nonhaemolytic jaundice", "constitutional hyperbilirubinemia", "Constitutional hyperbilirubinemia", "constitutional; hyperbilirubinemia", "Constitutional hepatic dysfunction", "Hyperbilirubinemia, constitutional", "hyperbilirubinemia; constitutional", "Familial nonhemolytic bilirubinemia", "bilirubinemia; familial nonhemolytic", "Familial nonhaemolytic bilirubinaemia", "Chronic intermittent juvenile jaundice", "HYPERBILIRUBINEMIA, CHRONIC UNCONJUGATED", "HYPERBILIRUBINEMIA, FAMILIAL UNCONJUGATED", "jaundice; nonhemolitic congenital familial", "nonhemolitic congenital familial; jaundice", "Benign unconjugated bilirubinemia syndrome", "Benign unconjugated bilirubinaemia syndrome", "Constitutional hepatic dysfunction syndrome", "Low-grade chronic hyperbilirubinemia syndrome", "constitutional hyperbilirubinemia (diagnosis)", "Low-grade chronic hyperbilirubinaemia syndrome", "Hyperbilirubinemia, unconjugated, chronic non-hemolytic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gilbert syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C1335491", "names": ["Primary Systemic ALK-Negative Anaplastic Large Cell Lymphoma", "Primary Systemic Anaplastic Large Cell Lymphoma, ALK-Negative"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Systemic Anaplastic Large Cell Lymphoma, ALK-Negative", "shortest_name_length": 60}
{"curie": "UMLS:C0265512", "names": ["Enostosis", "bone island", "Bone island", "bone islands", "Enostosis of bone", "Enostosis (diagnosis)", "Enostosis of bone (finding)", "Enostosis (morphologic abnormality)", "non-articular bone disorders enostosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone island", "shortest_name_length": 9}
{"curie": "UMLS:C0686589", "names": ["chronic leukemia in remission", "Chronic Leukemia in Remission", "Chronic leukemia in remission", "Chronic leukaemia in remission", "Chronic Leukemia (in Remission)", "Chronic leukemia (in remission)", "Chronic leukemia, NOS, in remission", "Chronic leukemia NOS (in remission)", "Chronic leukaemia, NOS, in remission", "Chronic leukaemia NOS (in remission)", "Chronic leukemia in remission (disorder)", "chronic leukemia in remission (diagnosis)", "Chronic leukemia of unspecified cell type in remission", "Chronic leukaemia of unspecified cell type in remission", "Chronic leukemia of unspecified cell type, in remission", "Chronic leukaemia of unspecified cell type, in remission"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic leukemia in remission", "shortest_name_length": 29}
{"curie": "UMLS:C1708954", "names": ["Mediastinal Germ Cell Tumor with Somatic-Type Malignancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mediastinal Germ Cell Tumor with Somatic-Type Malignancy", "shortest_name_length": 56}
{"curie": "UMLS:C3897533", "names": ["Stage III Primary Peritoneal Cancer", "Stage III Primary Peritoneal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Primary Peritoneal Cancer AJCC v7", "shortest_name_length": 35}
{"curie": "MONDO:0012381", "names": ["HHF5", "hyperinsulinism due to INSR deficiency", "familial hyperinsulinemic hypoglycemia 5", "HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 5", "hyperinsulinemic hypoglycemia, familial, 5", "Hyperinsulinemic Hypoglycemia, Familial, 5", "hyperinsulinemic hypoglycemia, familial, type 5", "Hyperinsulinism due to insulin receptor deficiency", "hyperinsulinemic hypoglycemia due to INSR deficiency", "Hyperinsulinism due to INSR (insulin receptor) deficiency", "Hyperinsulinism due to insulin receptor deficiency (disorder)", "hyperinsulinemic hypoglycemia due to insulin receptor deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperinsulinism due to INSR deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0013686", "names": ["MPDT", "CAV3-related distal myopathy", "distal myopathy, Tateyama type", "Distal myopathy, Tateyama type", "myopathy, distal, Tateyama type", "MYOPATHY, DISTAL, TATEYAMA TYPE", "Caveolin 3 related distal myopathy", "distal muscular dystrophy Tateyama type", "Caveolin 3 related distal myopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal myopathy, Tateyama type", "shortest_name_length": 4}
{"curie": "MONDO:0000914", "names": ["CASIL", "CADASIL", "cadasil", "CADASIL1", "CADASIL 1", "CADASIL type 1", "CADASIL syndrome", "CADASIL Syndrome", "CADASIL (diagnosis)", "hereditary multi-infarct dementia", "Hereditary multi-infarct dementia", "familial vascular leukoencephalopathy", "DEMENTIA, HEREDITARY MULTIINFARCT TYPE", "dementia, hereditary multi-infarct type", "Dementia, Hereditary Multi Infarct Type", "Dementia, Hereditary Multi-Infarct Type", "Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy", "cerebral arteriopathy with subcortical infarcts and leukoencephalopathy", "cerebral arteriopathy with subcortical infarcts and leukoencephalopathy 1", "Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy", "cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy", "Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy", "Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy", "Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy", "autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1", "CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1", "cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1", "Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1", "shortest_name_length": 5}
{"curie": "MONDO:0007361", "names": ["Quincke edema", "C1 inhibitor deficiency", "Complement Component 4, Partial Deficiency Of", "COMPLEMENT COMPONENT 4, PARTIAL DEFICIENCY OF", "complement component 4, partial deficiency OF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "C1 inhibitor deficiency", "shortest_name_length": 13}
{"curie": "UMLS:C0024649", "names": ["Malposition of Heart and Cardiac Apex", "Malposition of heart and cardiac apex"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malposition of heart and cardiac apex", "shortest_name_length": 37}
{"curie": "MONDO:0011782", "names": ["Knapp streaks", "Angioid Streak", "angioid streaks", "Streak, Angioid", "Angioid streaks", "ANGIOID STREAKS", "Angioid Streaks", "Streaks, Angioid", "Angioid streaks, retina", "Laquer cracks of the retina", "Angioid streaks of the retina", "Angioid streaks of the fundus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angioid streaks", "shortest_name_length": 13}
{"curie": "MONDO:0012081", "names": ["AUTS4", "dup(15)(q11q13)", "Dup(15)(q11q13)", "Trisomy 15q11q13", "trisomy 15q11q13", "trisomy 15q11-q13", "autism susceptibility 4", "AUTISM, SUSCEPTIBILITY TO, 4", "autism, susceptibility to, 4", "15q11q13 duplication syndrome", "Duplication 15Q11-q13 syndrome", "DUPLICATION 15q11-q13 SYNDROME", "15q11-q13 duplication syndrome", "Duplication 15q11-q13 Syndrome", "15q11q13 microduplication syndrome", "15q11-q13 microduplication syndrome", "CHROMOSOME 15q11.2 DUPLICATION SYNDROME", "chromosome 15Q11.2 Duplication syndrome", "CHROMOSOME 15q11-q13 DUPLICATION SYNDROME", "Chromosome 15q11-q13 Duplication Syndrome", "chromosome 15q11-q13 DUPLICATION syndrome", "15q11q13 microduplication syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "15q11q13 microduplication syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C5447360", "names": ["Functional defects", "Immunodeficiency due to Functional Defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immunodeficiency due to Functional Defects", "shortest_name_length": 18}
{"curie": "MONDO:0001044", "names": ["atresia esophagus", "Atresia esophagus", "ATRESIA ESOPHAGUS", "esophagus atresia", "atresia; esophagus", "ESOPHAGEAL ATRESIA", "atresia esophageal", "Esophagus--Atresia", "esophageal atresia", "ESOPHAGUS, ATRESIA", "Esophageal Atresia", "Atresia oesophagus", "esophagus; atresia", "Esophageal atresia", "OESOPHAGEAL ATRESIA", "Atresia, Esophageal", "oesophageal atresia", "Esophageal Atresias", "Oesophageal atresia", "Atresia of esophagus", "atresia of esophagus", "Atresias, Esophageal", "Esophagus imperforate", "imperforate esophagus", "Imperforate esophagus", "Atresia of oesophagus", "esophagus; imperforate", "Imperforate oesophagus", "imperforate; esophagus", "Oesophagus imperforate", "OA - Esophageal atresia", "OA - Oesophageal atresia", "Atresia of esophagus NOS", "esophageal atresia (disease)", "congenital esophageal atresia", "Congenital Esophageal Atresia", "Congenital atresia of esophagus", "Congenital Atresia of Esophagus", "congenital atresia of esophagus", "Congenital imperforate esophagus", "congenital imperforate esophagus", "Congenital atresia of oesophagus", "Congenital atresia of esophagus (disorder)", "Birth defect in which part of esophagus did not develop", "Birth defect in which part of oesophagus did not develop"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophageal atresia", "shortest_name_length": 17}
{"curie": "MONDO:0009337", "names": ["HKLLS1", "CCBE1 Hennekam syndrome", "Lymphatic Dysplasia, Generalized", "lymphatic dysplasia, generalized", "LYMPHATIC DYSPLASIA, GENERALIZED", "Hennekam syndrome caused by mutation in CCBE1", "Hennekam lymphangiectasia-lymphedema syndrome", "Hennekam lymphangiectasia-lymphedema syndrome 1", "HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 1", "Hennekam lymphangiectasia-lymphedema syndrome type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hennekam lymphangiectasia-lymphedema syndrome 1", "shortest_name_length": 6}
{"curie": "MONDO:0007648", "names": ["LBC", "HDGC", "FDGC", "DGLBC", "diffuse gastric cancer", "familial gastric cancer", "gastric cancer, familial", "signet cell adenocarcinoma", "signet ring gastric carcinoma", "Familial diffuse gastric cancer", "familial diffuse gastric cancer", "Gastric Cancer, Familial Diffuse", "Hereditary Diffuse Gastric Cancer", "hereditary diffuse gastric cancer", "Hereditary diffuse gastric cancer", "GASTRIC CANCER, HEREDITARY DIFFUSE", "signet ring cell gastric carcinoma", "gastric cancer, hereditary diffuse", "Familial diffuse cancer of stomach", "familial diffuse cancer of stomach", "hereditary diffuse cancer of stomach", "Hereditary diffuse cancer of stomach", "hereditary diffuse carcinoma of stomach", "Hereditary diffuse carcinoma of stomach", "Hereditary Diffuse Gastric Adenocarcinoma", "hereditary diffuse gastric adenocarcinoma", "Hereditary diffuse gastric adenocarcinoma", "Hereditary Gastric Diffuse Adenocarcinoma", "gastric malignant carcinoma hereditary diffuse", "E-cadherin-associated hereditary gastric cancer", "Hereditary diffuse carcinoma of stomach (disorder)", "DIFFUSE GASTRIC AND LOBULAR BREAST CANCER SYNDROME", "hereditary diffuse carcinoma of stomach (diagnosis)", "GASTRIC CANCER, FAMILIAL DIFFUSE BREAST CANCER, LOBULAR"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary diffuse gastric adenocarcinoma", "shortest_name_length": 3}
{"curie": "MONDO:0005822", "names": ["syphilis latent", "latent syphilis", "SYPHILIS LATENT", "Latent Syphilis", "Latent syphilis", "SYPHILIS, LATENT", "syphilis; latent", "Syphilis, Latent", "latent; syphilitic", "Latent syphilis NOS", "SYPHILIS, INAPPARENT", "Latent Stage Syphilis", "Syphilis, Latent Stage", "Latent syphilis (disorder)", "latent syphilis (diagnosis)", "Latent syphilis, unspecified", "Latent syphilis, unspecified as early or late"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "latent syphilis", "shortest_name_length": 15}
{"curie": "MONDO:0004088", "names": ["cervical basaloid carcinoma", "Cervical Basaloid Carcinoma", "Cervical Basaloid Squamous Cell Carcinoma", "cervical basaloid squamous cell carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical basaloid carcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0013332", "names": ["Tsukahara syndrome", "Tsukahara Syndrome", "TSUKAHARA SYNDROME", "Giuffré-Tsukahara syndrome", "Giuffre Tsukahara syndrome", "Radioulnar synostosis-microcephaly-scoliosis syndrome", "radioulnar synostosis with microcephaly and scoliosis syndrome", "Radioulnar synostosis with microcephaly and scoliosis syndrome", "Radioulnar synostosis with microcephaly and scoliosis syndrome (disorder)", "radioulnar synostosis with microcephaly and scoliosis syndrome (diagnosis)", "Radioulnar Synostosis with Microcephaly, Short Stature, Scoliosis, and Mental Retardation", "BRACHYDACTYLY, TYPE A1, WITH SHORT STATURE, SCOLIOSIS, MICROCEPHALY, PTOSIS, HEARING LOSS, AND MENTAL RETARDATION", "brachydactyly, type A1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and mental retardation", "brachydactyly, type A1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly, type A1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and intellectual disability", "shortest_name_length": 18}
{"curie": "UMLS:C0278733", "names": ["Stage IV Vulvar Cancer", "Vulval cancer stage IV", "stage IV vulvar cancer", "Stage IV Vulva Cancer AJCC v6", "FIGO Stage IV Vulva Carcinoma", "AJCC Stage IV Vulva Cancer v6", "Vulva Cancer Stage IV AJCC v6", "Stage IV Vulvar Cancer AJCC v6", "Vulval Cancer Stage IV AJCC v6", "FIGO Stage IV Vulvar Carcinoma", "FIGO Stage IV Carcinoma of Vulva", "FIGO Stage IV Carcinoma of the Vulva"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Vulvar Cancer AJCC v6", "shortest_name_length": 22}
{"curie": "MONDO:0044645", "names": ["familial monosomy 7 syndrome", "monosomy 7 myelodysplasia and leukemia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial monosomy 7 syndrome", "shortest_name_length": 28}
{"curie": "UMLS:C1336433", "names": ["Stage IV Ovarian Yolk Sac Tumor", "Ovarian Yolk Sac Tumor Stage IV", "Yolk Sac Tumor of Ovary Stage IV", "Yolk Sac Tumor of the Ovary Stage IV", "Stage IV Ovarian Yolk Sac Tumor AJCC v7", "Stage IV Ovarian Yolk Sac Tumor AJCC v6", "Stage IV Ovarian Yolk Sac Tumor AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Ovarian Yolk Sac Tumor AJCC v6 and v7", "shortest_name_length": 31}
{"curie": "UMLS:C1707588", "names": ["Cutaneous Nasal Type Extranodal NK/T-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous Nasal Type Extranodal NK/T-Cell Lymphoma", "shortest_name_length": 50}
{"curie": "MONDO:0008544", "names": ["Sommer Hines syndrome", "Sommer-Hines syndrome", "Tetramelic monodactyly", "Tetramelic Monodactyly", "tetramelic monodactyly", "TETRAMELIC MONODACTYLY", "Tetramelic monodactyly (disorder)", "tetramelic monodactyly with autosomal dominant inheritance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tetramelic monodactyly", "shortest_name_length": 21}
{"curie": "UMLS:C1096272", "names": ["vanishing bile duct syndrome", "Vanishing bile duct syndrome", "bile duct syndrome vanishing", "Vanishing bile duct syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vanishing bile duct syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0001464", "names": ["Sigmoid Cancer", "sigmoid cancer", "cancer sigmoid", "Cancer, Sigmoid", "Sigmoidal Cancer", "Ca sigmoid colon", "Cancer of Sigmoid", "cancer colon sigmoid", "Sigmoid Colon Cancer", "cancer sigmoid colon", "Sigmoid colon cancer", "sigmoid colon cancer", "Colon Cancer, Sigmoid", "Cancer of the Sigmoid", "Cancer, Sigmoid Colon", "cancer of sigmoid colon", "malignant sigmoid colon neoplasm", "Malignant tumor of sigmoid colon", "malignant tumor of sigmoid colon", "Malignant tumour of sigmoid colon", "malignant neoplasm of sigmoid colon", "Malignant neoplasm of sigmoid colon", "Malignant tumor of sigmoid colon (disorder)", "malignant neoplasm of sigmoid colon (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sigmoid colon cancer", "shortest_name_length": 14}
{"curie": "MONDO:0007550", "names": ["EBS1A", "EBSDM", "EBS-DM", "EBS-gen sev", "EBS, generalized severe", "Dowling-Meara epidermolysis bullosa", "Simplex epidermolysis bullosa herpetiformis", "Epidermolysis bullosa simplex herpetiformis", "epidermolysis bullosa simplex, herpetiformis", "Autosomal dominant generalized EBS, severe form", "epidermolysis bullosa simplex Dowling-Meara type", "Dowling-Meara type epidermolysis bullosa simplex", "generalized severe epidermolysis bullosa simplex", "epidermolysis bullosa simplex, generalized severe", "EPIDERMOLYSIS BULLOSA SIMPLEX, DOWLING-MEARA TYPE", "Epidermolysis Bullosa Simplex, Dowling Meara Type", "epidermolysis bullosa simplex, Dowling-Meara type", "Epidermolysis Bullosa Herpetiformis Dowling Meara", "Epidermolysis Bullosa Herpetiformis Dowling-Meara", "Epidermolysis bullosa simplex, Dowling-Meara type", "Epidermolysis Bullosa Simplex, Dowling-Meara Type", "Epidermolysis Bullosa Herpetiformis, Dowling-Meara", "Epidermolysis Bullosa Herpetiformis, Dowling Meara", "EPIDERMOLYSIS BULLOSA SIMPLEX 1A, GENERALIZED SEVERE", "EPIDERMOLYSIS BULLOSA SIMPLEX 1A, DOWLING-MEARA TYPE", "epidermolysis bullosa simplex 1A, generalized severe", "epidermolysis bullosa herpetiformis Dowling-Meara type", "Epidermolysis bullosa simplex herpetiformis (disorder)", "Epidermolysis Bullosa Herpetiformis, Dowling-Meara Type", "Epidermolysis Bullosa Herpetiformis, Dowling Meara Type", "EPIDERMOLYSIS BULLOSA HERPETIFORMIS, DOWLING-MEARA TYPE", "epidermolysis bullosa herpetiformis, Dowling-Meara type", "Autosomal dominant generalized epidermolysis bullosa simplex, severe form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolysis bullosa simplex 1A, generalized severe", "shortest_name_length": 5}
{"curie": "UMLS:C0855196", "names": ["Testicular embryonal carcinoma stage III", "Stage III Testicular Embryonal Carcinoma", "Stage III Testicular Embryonal Carcinoma AJCC v7", "Stage III Testicular Embryonal Carcinoma AJCC v6", "Stage III Testicular Embryonal Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular embryonal carcinoma stage III", "shortest_name_length": 40}
{"curie": "MONDO:0013179", "names": ["SPG44", "hereditary spastic paraplegia 44", "hereditary spastic paraplegia type 44", "autosomal recessive spastic paraplegia 44", "Spastic Paraplegia 44, Autosomal Recessive", "SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE", "spastic paraplegia 44, autosomal recessive", "autosomal recessive spastic paraplegia type 44", "Autosomal recessive spastic paraplegia type 44", "GJC2 autosomal recessive complex spastic paraplegia", "familial spastic paraplegia autosomal recessive type 44", "Autosomal recessive spastic paraplegia type 44 (disorder)", "Autosomal recessive spastic paraplegia type 44 (diagnosis)", "autosomal recessive complex spastic paraplegia caused by mutation in GJC2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 44", "shortest_name_length": 5}
{"curie": "UMLS:C2828017", "names": ["Stage IIIB Merkel Cell Carcinoma", "Stage IIIB Merkel Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Merkel Cell Carcinoma AJCC v7", "shortest_name_length": 32}
{"curie": "UMLS:C0151565", "names": ["COLITIS HEMORRHAGIC", "Hemorrhagic colitis", "hemorrhagic colitis", "Colitis hemorrhagic", "HEMORRHAGIC COLITIS", "Colitis haemorrhagic", "haemorrhagic colitis", "COLITIS HAEMORRHAGIC", "Haemorrhagic colitis", "Hemorrhagic colitis, NOS", "Haemorrhagic colitis, NOS", "Hemorrhagic colitis (disorder)", "hemorrhagic colitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemorrhagic colitis", "shortest_name_length": 19}
{"curie": "MONDO:0011527", "names": ["CHN", "CHN1", "CMT4E", "CMT 4E", "Lyon's hypomyelinating neuropathy", "Hypomyelination, severe congenital", "hypomyelination, Severe congenital", "HYPOMYELINATION, SEVERE CONGENITAL", "Charcot Marie Tooth disease type 4E", "Charcot-Marie-Tooth disease type 4E", "Charcot-Marie-Tooth disease, type 4E", "Charcot-Marie-Tooth disease, Type 4E", "CHARCOT-MARIE-TOOTH DISEASE, TYPE 4E", "congenital hypomyelination neuropathy", "Congenital hypomyelinating neuropathy", "Congenital Hypomyelinating Neuropathy", "neuropathy, congenital hypomyelinating", "Charcot-Marie-Tooth neuropathy type 4E", "Neuropathy, congenital hypomyelinating", "Charcot-Marie-Tooth Neuropathy, Type 4e", "Charcot-Marie-Tooth neuropathy, type 4E", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4E", "hypomyelinating neuropathy, congenital, 1", "Neuropathy, congenital hypomyelinating, 1", "neuropathy, congenital hypomyelinating, 1", "congenital hypomyelinating neuropathy (CHN)", "Congenital hypomyelinating neuropathy (CHN)", "Charcot-Marie-Tooth disease type 4E (disorder)", "Charcot-Marie-Tooth disease type 4E (diagnosis)", "Congenital hypomyelinating neuropathy (disorder)", "Autosomal recessive congenital hypomyelinating neuropathy", "autosomal recessive congenital hypomyelinating neuropathy", "neuropathy, congenital hypomyelinating, autosomal dominant", "NEUROPATHY, CONGENITAL HYPOMYELINATING, 1, AUTOSOMAL DOMINANT", "NEUROPATHY, CONGENITAL HYPOMYELINATING, 1, AUTOSOMAL RECESSIVE", "autosomal recessive congenital hypomyelinating or amyelinating neuropathy", "NEUROPATHY, CONGENITAL HYPOMYELINATING OR AMYELINATING, AUTOSOMAL RECESSIVE", "neuropathy, congenital hypomyelinating or AMYELINATING, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 4E", "shortest_name_length": 3}
{"curie": "UMLS:C1336128", "names": ["Cervical Cancer Stage IB1", "Stage IB1 Cervical Cancer", "AJCC Stage IB1 Cervical Cancer", "FIGO Stage IB1 Cervix Carcinoma", "Stage IB1 Cervical Cancer AJCC v7", "Stage IB1 Cervical Cancer AJCC v6", "FIGO Stage IB1 Cervical Carcinoma", "FIGO Stage IB1 Carcinoma of Cervix", "FIGO Stage IB1 Cervix Uteri Carcinoma", "FIGO Stage IB1 Carcinoma of the Cervix", "FIGO Stage IB1 Uterine Cervix Carcinoma", "FIGO Stage IB1 Carcinoma of Cervix Uteri", "Stage IB1 Cervical Cancer AJCC v6 and v7", "FIGO Stage IB1 Carcinoma of Uterine Cervix", "FIGO Stage IB1 Carcinoma of the Cervix Uteri", "FIGO Stage IB1 Carcinoma of the Uterine Cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB1 Cervical Cancer", "shortest_name_length": 25}
{"curie": "MONDO:0005607", "names": ["CHRONIC BRONCHITIS", "Bronchitis;chronic", "BRONCHITIS CHRONIC", "Chronic bronchitis", "Chronic Bronchitis", "Bronchitis chronic", "chronic bronchitis", "bronchitis, chronic", "Bronchitis, Chronic", "bronchitis; chronic", "chronic; bronchitis", "BRONCHITIS, CHRONIC", "Bronchitis chronic NOS", "Chronic bronchitis NOS", "Chronic bronchitis, NOS", "Chronic emphysema syndrome", "Chronic bronchitis (disorder)", "chronic bronchitis (diagnosis)", "Unspecified chronic bronchitis", "Chronic bronchitis, unspecified", "Chronic bronchitis, clinical syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic bronchitis", "shortest_name_length": 18}
{"curie": "MONDO:0013016", "names": ["IADD", "LAD3", "LAD1V", "LAD-3", "lad-III", "LAD-III", "LAD1 variant", "lad-1 variant", "LAD-1 variant", "LEUKOCYTE ADHESION DEFICIENCY 3", "Leukocyte Adhesion Deficiency 3", "leukocyte adhesion deficiency 3", "Leukocyte Adhesion Deficiency Type 3", "FERMT3 leukocyte adhesion deficiency", "leukocyte adhesion deficiency type 3", "leukocyte adhesion deficiency, type 3", "integrin Activation deficiency disease", "integrin activation deficiency disease", "Integrin Activation Deficiency Disease", "INTEGRIN ACTIVATION DEFICIENCY DISEASE", "Leukocyte adhesion deficiency type III", "leukocyte adhesion deficiency type III", "Leukocyte Adhesion Deficiency, Type III", "leukocyte adhesion deficiency-1 variant", "Leukocyte Adhesion Deficiency 1 Variant", "LEUKOCYTE ADHESION DEFICIENCY 1 VARIANT", "Leukocyte adhesion deficiency-1 variant", "leukocyte adhesion deficiency 1 variant", "leukocyte adhesion deficiency, type III", "LEUKOCYTE ADHESION DEFICIENCY, TYPE III", "leukocyte adhesion deficiency caused by mutation in FERMT3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukocyte adhesion deficiency 3", "shortest_name_length": 4}
{"curie": "MONDO:0008073", "names": ["HNFJ", "FJHN", "HNFJ1", "MCKD2", "Mckd2", "ADTKD1", "ADMCKD2", "ADTKD-UMOD", "FJHN type 1", "Juvenile gout", "UMOD-related ADTKD", "UMOD-associated FJHN", "uromodulin storage disease", "Uromodulin Storage Disease", "Familial Gouty Nephropathy", "UMOD-related kidney disease", "Umod-Related Kidney Disease", "Familial Gout-Kidney Disease", "familial nephropathy with gout", "Nephropathy, familial, with gout", "nephropathy, familial, with gout", "MEDULLARY CYSTIC KIDNEY DISEASE 2", "medullary cystic kidney disease 2", "familial juvenile gouty nephropathy", "uromodulin-associated kidney disease", "gouty nephropathy, familial juvenile", "Uromodulin-Associated Kidney Disease", "GOUTY NEPHROPATHY, FAMILIAL JUVENILE", "Gouty nephropathy, familial juvenile", "Medullary Cystic Kidney Disease Type 2", "medullary cystic kidney disease type 2", "Medullary Cystic Kidney Disease Type II", "medullary cystic kidney disease type II", "Familial Juvenile Hyperuricemic Nephropathy", "FAMILIAL JUVENILE HYPERURICEMIC NEPHROPATHY", "familial juvenile hyperuricaemic nephropathy", "Hyperuricemic Nephropathy, Familial Juvenile", "hyperuricemic nephropathy, familial juvenile", "Hyperuricemic Nephropathy, Familial Juvenile 1", "HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 1", "hyperuricemic nephropathy, familial juvenile, 1", "UMOD familial juvenile hyperuricemic nephropathy", "familial juvenile hyperuricemic nephropathy type 1", "hyperuricemic nephropathy, familial juvenile, type 1", "medullary cystic kidney disease 2, autosomal dominant", "MEDULLARY CYSTIC KIDNEY DISEASE 2, AUTOSOMAL DOMINANT", "tubulointerstitial kidney disease, autosomal dominant, 1", "TUBULOINTERSTITIAL KIDNEY DISEASE, AUTOSOMAL DOMINANT, 1", "autosomal dominant medullary cystic kidney disease type 2", "UMOD-associated familial juvenile hyperuricemic nephropathy", "UMOD-related autosomal dominant tubulointerstitial kidney disease", "Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria", "glomerulocystic kidney disease with hyperuricemia and isosthenuria", "GLOMERULOCYSTIC KIDNEY DISEASE WITH HYPERURICEMIA AND ISOSTHENURIA", "autosomal dominant medullary cystic kidney disease with hyperuricemia", "familial juvenile hyperuricemic nephropathy caused by mutation in UMOD", "autosomal dominant tubulointerstitial kidney disease due to mutations in UMOD"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial juvenile hyperuricemic nephropathy type 1", "shortest_name_length": 4}
{"curie": "MONDO:0009376", "names": ["CPS1D", "CPS deficiency", "CAPS deficiency", "CPS1 deficiency", "CPS 1 deficiency", "CPS I DEFICIENCY", "CPS I deficiency", "deficiency disease", "Hyperammonemia, type I", "carbamoyl-phosphate synthase", "congenital hyperammonemia type I", "Congenital hyperammonemia, type I", "Congenital hyperammonaemia, type I", "Carbamylphosphate synthetase deficiency", "Carbamoyl-phosphate synthase deficiency", "carbamyl phosphate synthetase deficiency", "Carbamoyl Phosphate Synthetase Deficiency", "Carbamoyl phosphate synthetase deficiency", "Carbomyl-phosphate synthethase deficiency", "carbamoyl phosphate synthetase deficiency", "Carbamoyl-phosphate synthetase deficiency", "carbamoyl-phosphate synthetase deficiency", "carbamoylphosphate synthetase I deficiency", "carbamoyl phosphate synthetase 1 deficiency", "carbamoyl-phosphate synthetase 1 deficiency", "CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY", "carbamoyl-phosphate synthetase I deficiency", "Carbamoyl-phosphate synthetase I deficiency", "Carbamoyl-Phosphate Synthetase I Deficiency", "Carbamoyl-phosphate synthetase 1 deficiency", "CPS - Carbamoyl-phosphate synthase deficiency", "carbamyl phosphate synthetase (CPS) deficiency", "Carbamyl Phosphate Synthetase Deficiency Disease", "Carbamoyl Phosphate Synthase 1 Deficiency Disease", "Carbamoyl-Phosphate Synthase I Deficiency Disease", "Carbamoyl-Phosphate Synthase 1 Deficiency Disease", "Carbamyl-Phosphate Synthetase 1 Deficiency Disease", "Carbamyl-Phosphate Synthetase I Deficiency Disease", "Carbamyl Phosphate Synthetase I Deficiency Disease", "CPS1 (carbamoyl-phosphate synthetase 1) deficiency", "Carbamoylphosphate Synthetase I Deficiency Disease", "Carbamoylphosphate Synthetase 1 Deficiency Disease", "Carbamyl Phosphate Synthetase 1 Deficiency Disease", "Carbamoyl Phosphate Synthetase I Deficiency Disease", "Carbamoyl-Phosphate Synthetase I Deficiency Disease", "carbamoyl phosphate synthetase I deficiency disease", "Carbamoylphosphate Synthetase 1 Deficiency Disease -", "carbamoyl phosphate synthetase deficiency (diagnosis)", "Carbamoyl-phosphate synthetase 1 deficiency (disorder)", "Carbamoyl Phosphate Synthase (Ammonia) Deficiency Disease", "Hyperammonemia Due to Carbamoyl Phosphate Synthetase 1 Deficiency", "hyperammonemia due to carbamoyl phosphate synthetase 1 deficiency", "carbamoyl phosphate synthetase I deficiency, hyperammonemia due to", "CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY, HYPERAMMONEMIA DUE TO", "Carbamoyl Phosphate Synthetase I Deficiency, Hyperammonemia Due To", "carbamoyl phosphate synthetase 1 deficiency, hyperammonemia due to", "Carbamoyl-Phosphate Synthase 1 Deficiency Disease (Ornithine Carbamoyl Phosphate Deficiency)", "Carbamoyl Phosphate Synthase 1 Deficiency Disease (Ornithine Carbamoyl Phosphate Deficiency)", "Carbamoyl-Phosphate Synthase I Deficiency Disease (Ornithine Carbamoyl Phosphate Deficiency)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carbamoyl phosphate synthetase I deficiency disease", "shortest_name_length": 5}
{"curie": "MONDO:0016168", "names": ["CAPS", "caps", "Cryopyrinopathy", "Cryopyrinopathies", "Cryopyrin-Associated Periodic Syndrome", "Cryopyrin Associated Periodic Syndrome", "Cryopyrin-associated periodic syndrome", "cryopyrin-associated periodic syndrome", "Cryopyrin associated periodic syndrome", "cryopyrin-associated periodic syndromes", "Cryopyrin-associated periodic syndromes", "Cryopyrin-Associated Periodic Syndromes", "Cryopyrin Associated Periodic Syndromes", "Cryopyrin associated periodic syndrome (disorder)", "NLRP3-associated systemic autoinflammatory disease", "cryopyrin-associated periodic syndromes (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cryopyrin-associated periodic syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0009774", "names": ["OEIS complex", "OEIS syndrome", "cloaca exstrophy", "Cloacal exstrophy", "cloacal exstrophy", "exstrophy of cloaca", "Exstrophy of cloaca", "cloacal exstrophy sequence", "cloacal exstrophy (disease)", "Exstrophy of cloaca sequence", "bladder exstrophy cloacal exstrophy", "cloacal exstrophy of urinary bladder", "Cloacal exstrophy of urinary bladder", "Omphalocele exstrophy imperforate anus", "Exstrophy of cloaca sequence (disorder)", "cloacal exstrophy of urinary bladder (diagnosis)", "omphalocele-exstrophy-imperforate anus-spinal defects", "omphalocele - cloacal exstrophy - imperforate anus - spinal defect", "omphalocele-cloacal exstrophy-imperforate anus-spinal defect syndrome", "omphalocele, exstrophy of the cloaca, imperforate anus, and spinal defects", "omphalocele, exstrophy of the cloaca, imperforate anus, and spinal defects complex"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cloacal exstrophy", "shortest_name_length": 12}
{"curie": "UMLS:C1332522", "names": ["Benign Orbit Hemangiopericytoma", "Benign Hemangiopericytoma of Orbit", "Benign Hemangiopericytoma of the Orbit"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Orbit Hemangiopericytoma", "shortest_name_length": 31}
{"curie": "MONDO:0010381", "names": ["TNPS", "TN syndrome", "Tn Syndrome", "TN POLYAGGLUTINATION SYNDROME", "Tn polyagglutination syndrome", "GALACTOSYLTRANSFERASE DEFICIENCY", "Galactosyltransferase Deficiency", "galactosyltransferase deficiency", "Polyagglutinable erythrocyte syndrome", "Tn polyagglutination syndrome, somatic", "Polyagglutinable erythrocyte syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tn polyagglutination syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C2984110", "names": ["Oropharyngeal Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oropharyngeal Carcinoma by AJCC v7 Stage", "shortest_name_length": 40}
{"curie": "UMLS:C5418779", "names": ["Recurrent Primary Peritoneal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Primary Peritoneal Adenocarcinoma", "shortest_name_length": 43}
{"curie": "UMLS:C0346979", "names": ["bone marrow metastasis", "Metastases to bone marrow", "Metastasis to bone marrow", "Metastases to the Bone Marrow", "Metastasis to the Bone Marrow", "Cancer metastatic to bone marrow", "Metastatic Tumor to the Bone Marrow", "Metastatic Neoplasm to the Bone Marrow", "secondary malignant neoplasm bone marrow", "secondary malignant neoplasm of bone marrow", "Secondary malignant neoplasm of bone marrow", "Metastatic malignant neoplasm of bone marrow", "Metastatic malignant neoplasm to bone marrow", "Metastatic Malignant Neoplasm in the Bone Marrow", "Metastatic Malignant Neoplasm to the Bone Marrow", "Secondary malignant neoplasm of bone marrow, NOS", "Metastatic malignant neoplasm to bone marrow, NOS", "secondary malignant neoplasm of bone marrow (diagnosis)", "Metastatic malignant neoplasm to bone marrow (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to bone marrow", "shortest_name_length": 22}
{"curie": "UMLS:C0280186", "names": ["Recurrent Diffuse Small Cleaved Cell Lymphoma", "relapsed adult diffuse small cleaved cell lymphoma", "adult diffuse small cleaved cell lymphoma, relapsed", "Recurrent Adult Diffuse Small Cleaved Cell Lymphoma", "recurrent adult diffuse small cleaved cell lymphoma", "adult diffuse small cleaved cell lymphoma, recurrent", "diffuse small cleaved cell lymphoma, adult, recurrent", "diffuse small cleaved cell lymphoma, recurrent, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Adult Diffuse Small Cleaved Cell Lymphoma", "shortest_name_length": 45}
{"curie": "UMLS:C5420846", "names": ["Adenoma of the Retinal Pigment Epithelium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenoma of the Retinal Pigment Epithelium", "shortest_name_length": 41}
{"curie": "UMLS:C0747154", "names": ["Soft Palate SCC", "SCC of Soft Palate", "SCC of the Soft Palate", "Soft Palate Squamous Cell Carcinoma", "Squamous Cell Carcinoma of Soft Palate", "PALATE CANCER SQUAMOUS CELL SOFT PALATE", "Squamous Cell Carcinoma of the Soft Palate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Soft Palate Squamous Cell Carcinoma", "shortest_name_length": 15}
{"curie": "MONDO:0004014", "names": ["ethmoid sinus ectopic meningioma", "ethmoid sinus primary ectopic meningioma", "Ethmoid Sinus Primary Ectopic Meningioma", "ethmoidal sinus primary ectopic meningioma", "Ethmoidal Sinus Primary Ectopic Meningioma", "primary ectopic meningioma of ethmoid sinus", "Primary Ectopic Meningioma of Ethmoid Sinus", "Primary Ectopic Meningioma of Ethmoidal Sinus", "primary Ectopic meningioma of ethmoidal sinus", "primary ectopic meningioma of ethmoidal sinus", "primary ectopic meningioma of the ethmoid sinus", "Primary Ectopic Meningioma of the Ethmoid Sinus", "Primary Ectopic Meningioma of the Ethmoidal Sinus", "primary ectopic meningioma of the ethmoidal sinus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ethmoid sinus ectopic meningioma", "shortest_name_length": 32}
{"curie": "MONDO:0013864", "names": ["CDLS4", "Cornelia de Lange syndrome 4", "Cornelia DE Lange syndrome 4", "CORNELIA DE LANGE SYNDROME 4", "RAD21 Cornelia de Lange syndrome", "Cornelia De Lange syndrome type 4", "Cornelia de Lange syndrome caused by mutation in RAD21", "CORNELIA DE LANGE SYNDROME 4 WITH OR WITHOUT MIDLINE BRAIN DEFECTS", "Cornelia De Lange syndrome 4 with or without midline brain defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cornelia de Lange syndrome 4", "shortest_name_length": 5}
{"curie": "MONDO:0018440", "names": ["AR dRTA", "autosomal recessive distal RTA", "Autosomal recessive distal RTA", "RTA, distal, autosomal recessive", "Autosomal recessive distal renal tubular acidosis", "autosomal recessive distal renal tubular acidosis", "Renal tubular acidosis, distal, autosomal recessive", "RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE", "autosomal recessive distal renal tubular acidosis (disease)", "distal renal tubular acidosis (disease), autosomal recessive", "Renal tubular acidosis, autosomal recessive with preserved hearing", "Renal Tubular Acidosis, Autosomal Recessive, With Preserved Hearing"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive distal renal tubular acidosis", "shortest_name_length": 7}
{"curie": "UMLS:C4683568", "names": ["Lugano Classification Stage IE Adult Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage IE Adult Lymphoma AJCC v8", "shortest_name_length": 53}
{"curie": "MONDO:0032756", "names": ["LQT8", "LONG QT SYNDROME 8", "long qt syndrome 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "long qt syndrome 8", "shortest_name_length": 4}
{"curie": "UMLS:C5206341", "names": ["Unresectable Colon Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Colon Adenocarcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0016374", "names": ["facial neuralgia", "Facial neuralgia", "neuralgia cranial", "cranial neuralgia", "Cranial neuralgia", "Cranial neuralgia (disorder)", "cranial neuron projection bundle neuralgia", "neuralgia of cranial neuron projection bundle"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cranial neuralgia", "shortest_name_length": 16}
{"curie": "UMLS:C1707042", "names": ["Breast Carcinoma with Chondroid Metaplasia", "Breast Carcinoma with Cartilaginous Metaplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Carcinoma with Chondroid Metaplasia", "shortest_name_length": 42}
{"curie": "MONDO:0005404", "names": ["CFS", "SEID", "ME/CFS", "Akureyri", "YUPPIE FLU", "yuppie flu", "Iceland disease", "ICELAND DISEASE", "Iceland; disease", "Akureyri disease", "Icelandic disease", "postviral fatigue", "Royal Free disease", "Royal Free Disease", "Myalgic encephalitis", "myalgic encephalitis", "FATIGUE CHRONIC SYNDROME", "Chronic Fatigue Syndrome", "chronic fatigue syndrome", "CHRONIC FATIGUE SYNDROME", "Epidemic neuromyasthenia", "Chronic Fatigue Disorder", "Chronic fatigue syndrome", "Chronic Fatigue Disorders", "Myalgic Encephalomyelitis", "Myalgic encephalomyelitis", "encephalomyelitis myalgic", "Fatigue Disorder, Chronic", "Fatigue Syndrome, Chronic", "NEUROMYASTHENIA, EPIDEMIC", "myalgic encephalomyelitis", "Chronic Fatigue Syndromes", "Encephalomyelitis, Myalgic", "Fatigue Syndromes, Chronic", "syndrome; fatigue, chronic", "myalgic; encephalomyelitis", "Postviral fatigue syndrome", "fatigue; syndrome, chronic", "encephalomyelitis; myalgic", "Fatigue Disorders, Chronic", "Postviral Fatigue Syndrome", "postviral fatigue syndrome", "POST-VIRAL FATIGUE SYNDROME", "Syndrome, Postviral Fatigue", "Postviral Fatigue Syndromes", "Fatigue Syndrome, Postviral", "Post viral fatigue syndrome", "fatigue syndrome; postviral", "post viral fatigue syndrome", "post-viral fatigue syndrome", "syndrome; postviral, fatigue", "Chronic fatigue, unspecified", "syndrome; fatigue, postviral", "fatigue; syndrome, postviral", "Syndromes, Postviral Fatigue", "postviral; syndrome, fatigue", "Fatigue Syndromes, Postviral", "chronic fatigue syndrome (CFS)", "ME - Myalgic encephalomyelitis", "CFS - Chronic fatigue syndrome", "CFS (chronic fatigue syndrome)", "Postviral fatigue syndrome, NOS", "Benign myalgic encephalomyelitis", "encephalomyelitis; benign myalgic", "benign; myalgic encephalomyelitis", "PVFS - Postviral fatigue syndrome", "Myalgic encephalomyelitis syndrome", "Chronic fatigue syndrome (disorder)", "ENCEPHALOMYELITIS, EPIDEMIC MYALGIC", "chronic fatigue syndrome (diagnosis)", "Chronic Fatigue Fibromyalgia Syndrome", "Systemic Exertion Intolerance Disease", "systemic exertion intolerance disease", "Chronic Fatigue-Fibromyalgia Syndrome", "Postviral fatigue syndrome (disorder)", "Chronic Fatigue-Fibromyalgia Syndromes", "Fatigue-Fibromyalgia Syndrome, Chronic", "postviral fatigue syndrome (diagnosis)", "Fatigue-Fibromyalgia Syndromes, Chronic", "chronic fatigue immune dysfunction syndrome", "Chronic Fatigue and Immune Dysfunction Syndrome", "chronic fatigue and immune dysfunction syndrome", "Infectious Mononucleosis Like Syndrome, Chronic", "Infectious Mononucleosis-Like Syndrome, Chronic", "Myalgic encephalomyelitis/chronic fatigue syndrome", "myalgic encephalomyelitis/chronic fatigue syndrome", "myalgic encephalomeyelitis/chronic fatigue syndrome", "myalgic encephalomyelitis/chronic fatigue syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myalgic encephalomeyelitis/chronic fatigue syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0035645", "names": ["inherited gynecological cancer-predisposing syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited gynecological cancer-predisposing syndrome", "shortest_name_length": 52}
{"curie": "MONDO:0005429", "names": ["TSE", "disease prion", "Prion disease", "Prion Disease", "prion disease", "Prion Diseases", "prion diseases", "disease prions", "PRION DISEASES", "Prion diseases", "diseases prion", "diseases prions", "Prion disease, NOS", "Human prion disease", "Prion protein disease", "prion disease pathway", "Prion disease pathway", "Prion Protein Disease", "prion protein disease", "Prion Protein Diseases", "Prion Induced Disorder", "prion induced disorder", "Transmissible Dementia", "Prion-Induced Disorder", "Transmissible Dementias", "Prion-Induced Disorders", "Disorder, Prion-Induced", "Dementia, Transmissible", "Dementias, Transmissible", "Prion disease (disorder)", "Disorders, Prion-Induced", "prion disease (diagnosis)", "spongiform encephalopathy", "Spongiform encephalopathy", "Spongiform Encephalopathy", "Prion-associated disorders", "Prion-Associated Disorders", "encephalopathy; spongiform", "spongiform; encephalopathy", "encephalopathies spongiform", "Spongiform encephalopathy (disorder)", "Transmissible spongiform encephalopathy", "Transmissible Spongiform Encephalopathy", "transmissible spongiform encephalopathy", "prion disease of central nervous system", "Spongiform Encephalopathy, Transmissible", "Encephalopathy, Transmissible Spongiform", "Transmissible Spongiform Encephalopathies", "Encephalopathies, Transmissible Spongiform", "Spongiform Encephalopathies, Transmissible", "Encephalopathies, Spongiform, Transmissible", "Transmissible Spongiform Encephalopathy(TSE)", "Prion diseases of the central nervous system NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prion disease", "shortest_name_length": 3}
{"curie": "MONDO:0021201", "names": ["Skin Infection", "Skin infection", "Infection;skin", "skin infection", "SKIN INFECTION", "infection; skin", "skin; infection", "Skin Infections", "Skin infections", "Skin--Infections", "Infection of skin", "infection of skin", "Skin infection NOS", "infectious skin disease", "Infectious Skin Disease", "Skin Disease, Infectious", "infectious skin diseases", "Disease, Infectious Skin", "Infectious Skin Diseases", "Diseases, Infectious Skin", "Skin Diseases, Infectious", "Infection of skin (disorder)", "infection of skin (diagnosis)", "Infective dermatological disorders", "Skin and subcutaneous tissue infection", "infections skin and subcutaneous tissue", "Skin and subcutaneous tissue infections", "INFECTIONS OF SKIN AND SUBCUTANEOUS TISSUE", "infections of skin and subcutaneous tissue", "Infection of skin and/or subcutaneous tissue", "Infection of skin and subcutaneous tissue, NOS", "Infections of the skin and subcutaneous tissue", "INFECTIONS OF THE SKIN AND SUBCUTANEOUS TISSUES", "infections of skin and subcutaneous tissue (diagnosis)", "Infection of skin and/or subcutaneous tissue (disorder)", "Infections of the skin and subcutaneous tissue (L00-L08)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin infection", "shortest_name_length": 14}
{"curie": "UMLS:C1736167", "names": ["Systemic allergic reaction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Systemic allergic reaction", "shortest_name_length": 26}
{"curie": "UMLS:C0348828", "names": ["Postprocedural Respiratory Disorder", "Postprocedural respiratory disorders", "Post-Procedural Respiratory Disorder", "Postprocedural respiratory disorders (disorder)", "Postprocedural respiratory disorder, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postprocedural respiratory disorders", "shortest_name_length": 35}
{"curie": "MONDO:0025163", "names": ["White Heifer Disease", "White heifer disease", "white heifer disease", "disease, White heifer", "Disease, White Heifer", "Segmental uterine aplasia", "Segmental uterine aplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "white heifer disease", "shortest_name_length": 20}
{"curie": "MONDO:0030847", "names": ["DA1C", "distal arthrogryposis type 1C", "arthrogryposis, distal, type 1C", "ARTHROGRYPOSIS, DISTAL, TYPE 1C"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis, distal, type 1C", "shortest_name_length": 4}
{"curie": "UMLS:C0271271", "names": ["Xerotic keratitis", "Xerotic Keratitis", "xerotic keratitis", "xerotic; keratitis", "keratitis; xerotic", "Xerotic keratitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Xerotic keratitis", "shortest_name_length": 17}
{"curie": "UMLS:C0524686", "names": ["Acute Nonsuppurative Periodontitis", "Nonsuppurative Periodontitis, Acute", "Periodontitis, Acute Nonsuppurative", "Acute Nonsuppurative Periodontitides", "Periodontitides, Acute Nonsuppurative", "Nonsuppurative Periodontitides, Acute"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Periodontitis, Acute Nonsuppurative", "shortest_name_length": 34}
{"curie": "UMLS:C0332428", "names": ["Lymphoma stage III", "Lymphoma Stage III", "Stage III Lymphoma", "Lymphoma stage III (finding)", "Ann Arbor Stage III Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoma stage III", "shortest_name_length": 18}
{"curie": "MONDO:0017342", "names": ["EBV-related tumor", "Epstein-Barr virus-related tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epstein-Barr virus-related tumor", "shortest_name_length": 17}
{"curie": "UMLS:C1709263", "names": ["Nonestrogen-Dependent Cancer", "Nonestrogen-Dependent Carcinoma", "Nonestrogen-Dependent Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nonestrogen-Dependent Malignant Neoplasm", "shortest_name_length": 28}
{"curie": "MONDO:0022481", "names": ["APO A-i deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "APO A-i deficiency", "shortest_name_length": 18}
{"curie": "UMLS:C0683357", "names": ["drinking; excess", "excessive drinking", "Excessive drinking", "drinking excessive", "drinking; excessive", "excessive; drinking"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Excessive drinking", "shortest_name_length": 16}
{"curie": "MONDO:0008015", "names": ["swing; nausea", "nausea; swing", "Riders' vertigo", "Travel Sickness", "Motion Sickness", "travel sickness", "Travel sickness", "motion sickness", "Motion sickness", "TRAVEL SICKNESS", "MOTION SICKNESS", "Sickness, Motion", "nausea; roundabout", "roundabout; nausea", "Travel sickness NOS", "Motion sickness, NOS", "Motion sickness (finding)", "motion sickness (diagnosis)", "travel sickness (diagnosis)", "nausea occurs with body motion while traveling", "disease (or disorder); travel sickness (any vehicle)", "nausea occurs with body motion while traveling (symptom)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "motion sickness", "shortest_name_length": 13}
{"curie": "UMLS:C0861727", "names": ["Pancreatic adenocarcinoma metastatic", "Metastatic Pancreatic Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic adenocarcinoma metastatic", "shortest_name_length": 36}
{"curie": "UMLS:C1336219", "names": ["Cervical Cancer Stage IIIB", "stage IIIB cervical cancer", "cervical cancer stage IIIB", "Stage IIIB Cervical Cancer", "AJCC stage IIIB cervical cancer", "AJCC Stage IIIB Cervical Cancer", "FIGO Stage IIIB Cervix Carcinoma", "FIGO stage IIIB cervix carcinoma", "Stage IIIB Cervical Cancer AJCC v6", "Stage IIIB Cervical Cancer AJCC v7", "stage IIIB cervical cancer AJCC v7", "FIGO stage IIIB cervical carcinoma", "FIGO Stage IIIB Cervical Carcinoma", "stage IIIB cervical cancer AJCC v6", "FIGO Stage IIIB Carcinoma of Cervix", "FIGO stage IIIB carcinoma of cervix", "FIGO stage IIIB cervix uteri carcinoma", "FIGO Stage IIIB Cervix Uteri Carcinoma", "FIGO stage IIIB carcinoma of the cervix", "FIGO Stage IIIB Carcinoma of the Cervix", "FIGO stage IIIB uterine cervix carcinoma", "FIGO Stage IIIB Uterine Cervix Carcinoma", "FIGO stage IIIB carcinoma of cervix uteri", "FIGO Stage IIIB Carcinoma of Cervix Uteri", "Stage IIIB Cervical Cancer AJCC v6 and v7", "FIGO Stage IIIB Carcinoma of Uterine Cervix", "FIGO stage IIIB carcinoma of uterine cervix", "FIGO Stage IIIB Carcinoma of the Cervix Uteri", "FIGO stage IIIB carcinoma of the cervix uteri", "FIGO Stage IIIB Carcinoma of the Uterine Cervix", "FIGO stage IIIB carcinoma of the uterine cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Cervical Cancer AJCC v6 and v7", "shortest_name_length": 26}
{"curie": "UMLS:C0346976", "names": ["metastasis pancreas", "pancreas metastases", "Pancreatic metastasis", "Metastases to pancreas", "Metastasis to pancreas", "metastatic pancreas cancer", "PANCREAS CANCER METASTATIC", "cancer metastatic pancreas", "pancreas cancer, metastatic", "Pancreatic cancer metastatic", "metastatic pancreatic cancer", "cancer metastatic pancreatic", "pancreatic cancer, metastatic", "Cancer metastatic to pancreas", "Metastatic Tumor to the Pancreas", "Secondary Cancer to the Pancreas", "Metastatic Cancer to the Pancreas", "Metastatic Neoplasm to the Pancreas", "Pancreas neoplasm malignant metastatic", "Secondary malignant deposit in pancreas", "pancreatic malignant neoplasm secondary", "Secondary malignant neoplasm of pancreas", "Secondary Malignant Tumor to the Pancreas", "Metastatic malignant neoplasm of pancreas", "Metastatic malignant neoplasm to pancreas", "Malignant neoplasm of pancreas metastatic", "Secondary Malignant Neoplasm to the Pancreas", "Metastatic Malignant Neoplasm in the Pancreas", "Metastatic Malignant Neoplasm to the Pancreas", "Secondary malignant neoplasm of pancreas, NOS", "Metastatic malignant neoplasm to pancreas, NOS", "Secondary malignant neoplasm of pancreas (diagnosis)", "Metastatic malignant neoplasm to pancreas (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to pancreas", "shortest_name_length": 19}
{"curie": "EFO:0010820", "names": ["spontaneous coronary artery dissection\"@e"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spontaneous coronary artery dissection\"@e", "shortest_name_length": 41}
{"curie": "MONDO:0013154", "names": ["MDDGA2", "muscle-eye-brain-POMT2 related", "congenital muscular dystrophy-dystroglycanopathy type A2", "Walker-Warburg syndrome or muscle-eye-brain disease, POMT2-related", "Walker-Warburg syndrome or muscle-eye-brain disease, Pomt2-related", "WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED", "congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A2", "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A2", "Muscular Dystrophy-Dystroglycanopathy (Congenital with Brain and Eye Anomalies) Type A, 2", "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type A, 2", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2", "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A2", "shortest_name_length": 6}
{"curie": "UMLS:C4524025", "names": ["Reaction to excipient"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reaction to excipient", "shortest_name_length": 21}
{"curie": "UMLS:C2316827", "names": ["Second trimester bleeding", "second trimester bleeding", "bleeding during second trimester", "Second trimester bleeding (disorder)", "second trimester bleeding (diagnosis)", "Second Trimester Antepartum Hemorrhage", "Antepartum Hemorrhage, Second Trimester", "antepartum hemorrhage - second trimester", "bleeding during second trimester (symptom)", "bleeding during the second trimester of pregnancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Second trimester bleeding", "shortest_name_length": 25}
{"curie": "MONDO:0016698", "names": ["ependymoma", "EPENDYMOMA", "Ependymoma", "Ependymomas", "ependymomas", "Ependymoma NOS", "CNS, ependymoma", "Ependymoma, NOS", "benign ependymoma", "ependymoma, benign", "Classic ependymoma", "ependymoma, familial", "epithelial ependymoma", "Ependymoma (disorder)", "Epithelial ependymoma", "WHO Grade 2 Ependymal Tumor", "WHO Grade II Ependymal Tumor", "WHO grade II Ependymal tumor", "WHO grade II ependymal tumor", "ependymoma; unspecified site", "WHO Grade 2 Ependymal Neoplasm", "WHO Grade II Ependymal Neoplasm", "WHO grade II ependymal neoplasm", "Ependymoma (morphologic abnormality)", "tanycytic ependymoma (histologic variant)", "papillary ependymoma (histologic variant)", "clear cell ependymoma (histologic variant)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ependymoma", "shortest_name_length": 10}
{"curie": "EFO:0009752", "names": ["visuospatial impairment"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "visuospatial impairment", "shortest_name_length": 23}
{"curie": "MONDO:0011122", "names": ["Obese", "obese", "OBESE", "Obesity", "obesity", "OBESITY", "Adiposity", "Obesities", "adiposity", "Obesity NOS", "Obesity, NOS", "obesity disease", "Obese (finding)", "obesity disorder", "Obesity (disorder)", "obesity (diagnosis)", "Obesity, unspecified", "Having too much body fat"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "obesity disorder", "shortest_name_length": 5}
{"curie": "MONDO:0002731", "names": ["Cerebral Cancer", "cancer cerebral", "cerebral cancer", "cerebrum cancer", "tumor of Cerebrum", "tumor of cerebrum", "neoplasm of cerebrum", "telencephalon cancer", "cancer of telencephalon", "malignant cerebral tumor", "Malignant Cerebral Tumor", "cerebral hemisphere cancer", "Malignant Tumor of Cerebrum", "malignant tumor of cerebrum", "malignant cerebral neoplasm", "Malignant Cerebral Neoplasm", "cancer of cerebral hemisphere", "Malignant Neoplasm of Cerebrum", "Malignant neoplasm of cerebrum", "malignant neoplasm of cerebrum", "malignant tumor of the cerebrum", "Malignant Tumor of the Cerebrum", "malignant telencephalon neoplasm", "brain tumor malignant of cerebrum", "malignant neoplasm of the cerebrum", "Malignant Neoplasm of the Cerebrum", "Malignant neoplasm of cerebrum, NOS", "malignant neoplasm of telencephalon", "malignant cerebral hemispheric tumor", "Malignant Cerebral Hemispheric Tumor", "malignant cerebral hemisphere neoplasm", "malignant tumor of cerebral hemisphere", "Malignant Tumor of Cerebral Hemispheres", "Malignant Cerebral Hemispheric Neoplasm", "malignant tumor of cerebral hemispheres", "malignant cerebral hemispheric neoplasm", "malignant neoplasm of cerebral hemisphere", "Malignant neoplasm of cerebrum (disorder)", "malignant neoplasm of cerebral hemispheres", "Malignant neoplasm of other parts of brain", "malignant neoplasm of cerebrum (diagnosis)", "Malignant Neoplasm of Cerebral Hemispheres", "malignant tumor of the cerebral hemispheres", "Malignant Tumor of the Cerebral Hemispheres", "Malignant Neoplasm of the Cerebral Hemispheres", "malignant neoplasm of the cerebral hemispheres", "malignant neoplasm of cerebral hemisphere (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral hemisphere cancer", "shortest_name_length": 15}
{"curie": "UMLS:C5239373", "names": ["Metastatic Choroid Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Choroid Melanoma", "shortest_name_length": 27}
{"curie": "MONDO:0008197", "names": ["PFM", "PFM1", "catlin Marks", "parietal foramina", "parietal foramina 1", "Parietal Foramina 1", "PARIETAL FORAMINA 1", "MSX2 parietal foramina", "cranium bifidum occultum", "cranium bifidum, hereditary", "foramina parietalia permagna", "parietal foramina, symmetric", "parietal foramina caused by mutation in MSX2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parietal foramina 1", "shortest_name_length": 3}
{"curie": "MONDO:0013618", "names": ["CAASDS", "craniofacial anomalies and anterior segment dysgenesis syndrome", "CRANIOFACIAL ANOMALIES AND ANTERIOR SEGMENT DYSGENESIS SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniofacial anomalies and anterior segment dysgenesis syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C0740401", "names": ["PERFORATION DUODENAL", "perforated duodenal ulcer", "PERFORATED DUODENAL ULCER", "duodenal perforated ulcer", "DUODENAL ULCER PERFORATED", "Ulcer;perforated;duodenal", "Duodenal ulcer perforated", "duodenal perforated ulcers", "Duodenal ulcer perforation", "duodenal ulcer perforation", "DUODENAL ULCER PERFORATION", "Perforation of duodenal ulcer", "DU - Perforated duodenal ulcer", "Ulcer duodenal with perforation", "Duodenal ulcer with perforation", "Duodenal ulcers and perforation", "ULCER DUODENAL WITH PERFORATION", "Duodenal ulcer, NOS with perforation", "peptic ulcer duodenal with perforation", "Duodenal ulcer with perforation (disorder)", "Duodenal ulcer with perforation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Duodenal ulcer perforation", "shortest_name_length": 20}
{"curie": "OMIM:227220", "names": ["BEY2", "HCL3", "SHEP1", "EYCL3", "EYE COLOR 3", "HAIR COLOR 3", "BROWN EYE COLOR 2", "EYE COLOR, BROWN/BLUE", "EYE COLOR, BLUE/NONBLUE", "SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 1", "SKIN/HAIR/EYE PIGMENTATION 1, BLUE/BROWN EYES", "SKIN/HAIR/EYE PIGMENTATION 1, BLOND/BROWN HAIR", "SKIN/HAIR/EYE PIGMENTATION 1, BLUE/NONBLUE EYES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 4}
{"curie": "MONDO:0032716", "names": ["ARLIAK", "acute reversible leukoencephalopathy due to SLC13A3 deficiency", "Acute reversible leukoencephalopathy due to SLC13A3 deficiency", "acute reversible leukoencephalopathy with increased urinary alpha-ketoglutarate", "Acute reversible leukoencephalopathy with increased urinary alpha-ketoglutarate", "leukoencephalopathy, acute reversible, with increased urinary alpha-ketoglutarate", "LEUKOENCEPHALOPATHY, ACUTE REVERSIBLE, WITH INCREASED URINARY ALPHA-KETOGLUTARATE", "acute reversible leukoencephalopathy due to sodium-dependent dicarboxylate transporter deficiency", "Acute reversible leukoencephalopathy due to sodium-dependent dicarboxylate transporter deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukoencephalopathy, acute reversible, with increased urinary alpha-ketoglutarate", "shortest_name_length": 6}
{"curie": "MONDO:0002423", "names": ["Rectosigmoid Tumor", "rectosigmoid tumor", "Rectosigmoid tumor", "Rectosigmoid Neoplasm", "rectosigmoid neoplasm", "rectosigmoid junction tumor", "rectosigmoid tumor or cancer", "tumor of rectosigmoid junction", "Tumor of rectosigmoid junction", "rectosigmoid junction neoplasm", "Tumor of Rectosigmoid Junction", "Tumour of rectosigmoid junction", "Neoplasm of Rectosigmoid Junction", "Neoplasm of rectosigmoid junction", "neoplasm of rectosigmoid junction", "Tumor of the Rectosigmoid Junction", "tumor of the rectosigmoid junction", "neoplasm of the rectosigmoid junction", "Neoplasm of the Rectosigmoid Junction", "rectosigmoid junction neoplasm (disease)", "Neoplasm of rectosigmoid junction (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rectosigmoid junction neoplasm", "shortest_name_length": 18}
{"curie": "MONDO:0010682", "names": ["myoclonic epilepsy, progressive", "myoclonic epilepsy, progressive, X-linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myoclonic epilepsy, progressive, X-linked", "shortest_name_length": 31}
{"curie": "MONDO:0003086", "names": ["Thymus Mucoepidermoid Carcinoma", "Thymus mucoepidermoid carcinoma", "thymic mucoepidermoid carcinoma", "thymus mucoepidermoid carcinoma", "Thymic Mucoepidermoid Carcinoma", "Mucoepidermoid Carcinoma of Thymus", "mucoepidermoid carcinoma of Thymus", "Mucoepidermoid Carcinoma of the Thymus", "mucoepidermoid carcinoma of the Thymus", "Mucoepidermoid carcinoma of the Thymus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thymic mucoepidermoid carcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C5238405", "names": ["Refractory Prostate Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Prostate Adenocarcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0015860", "names": ["anomaly of puberty or/and menstrual cycle"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anomaly of puberty or/and menstrual cycle", "shortest_name_length": 41}
{"curie": "MONDO:0003135", "names": ["GLOMERULONEPHRITIS, LOCAL", "Focal Embolic Glomerulonephritis", "focal embolic glomerulonephritis", "GLOMERULONEPHRITIS, FOCAL EMBOLIC", "GLOMERULONEPHRITIS PROLIFERATIVE FOCAL", "GLOMERULONEPHRITIS, FOCAL PROLIFERATIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal embolic glomerulonephritis", "shortest_name_length": 25}
{"curie": "UMLS:C0341037", "names": ["LPC", "periodontal lateral cyst", "Lateral periodontal cyst", "cyst periodontal lateral", "Lateral Periodontal Cyst", "lateral periodontal; cyst", "cyst; lateral periodontal", "cyst; periodontal, lateral", "periodontal; cyst, lateral", "lateral periodontal jaw cyst", "lateral developmental jaw cyst", "lateral periodontal cyst of jaw", "Lateral periodontal cyst of jaw", "Lateral developmental cyst of jaw", "lateral developmental cyst of jaw", "lateral periodontal cyst of jaw (diagnosis)", "Lateral developmental cyst of jaw (disorder)", "lateral developmental cyst of jaw (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lateral developmental cyst of jaw", "shortest_name_length": 3}
{"curie": "MONDO:0020118", "names": ["Delta granule disease", "dense granule disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dense granule disease", "shortest_name_length": 21}
{"curie": "UMLS:C4521815", "names": ["Stage IVA Appendix Cancer", "Stage IVA Appendix Carcinoma AJCC v8", "Stage IVA Appendiceal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Appendix Carcinoma AJCC v8", "shortest_name_length": 25}
{"curie": "MONDO:0001910", "names": ["Ochronoses", "ochronosis", "Ochronosis", "ochronoses", "Pseudo-ochronosis", "Ocular ochronosis", "ochronosis disorder", "Exogenous ochronosis", "ochronosis (diagnosis)", "Alcaptonuric ochronosis", "Alkaptonuric ochronosis", "Ochronosis due to alkaptonuria", "Exogenous ochronosis (disorder)", "Pigmentation due to alkaptonuria", "Ochronosis due to homogentisate 1,2-dioxygenase deficiency", "Ochronosis due to homogentisate 1,2-dioxygenase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ochronosis disorder", "shortest_name_length": 10}
{"curie": "UMLS:C1881154", "names": ["In-Hospital Cardiac Arrest"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "In-Hospital Cardiac Arrest", "shortest_name_length": 26}
{"curie": "MONDO:0016537", "names": ["Duncan's syndrome", "Lymphoproliferative disease", "lymphoproliferative disease", "Lymphoproliferative Disorder", "lymphoproliferative disorder", "Lymphoproliferative disorder", "Lymphoproliferative syndrome", "lymphoproliferative syndrome", "diseases lymphoproliferative", "lymphoproliferative disorders", "lymphoproliferative; disorder", "Lymphoproliferative Disorders", "disorders lymphoproliferative", "Disorder, Lymphoproliferative", "Lymphoproliferative disorders", "Disorders, Lymphoproliferative", "Lymphoproliferative disease NOS", "Lymphoproliferative disease, NOS", "Lymphoproliferative disorder NOS", "lymphoproliferative disorder nos", "Lymphoproliferative disorder, NOS", "lymphoproliferative disease (diagnosis)", "Lymphoproliferative disorder (disorder)", "disease (or disorder); lymphoproliferative", "Combined immunodeficiency due to ITK deficiency", "Lymphoproliferative disorder (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphoproliferative syndrome", "shortest_name_length": 17}
{"curie": "MONDO:0019016", "names": ["maternally-inherited CPEO", "maternally-inherited progressive external ophthalmoplegia", "maternally-inherited chronic progressive external ophthalmoplegia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maternally-inherited progressive external ophthalmoplegia", "shortest_name_length": 25}
{"curie": "UMLS:C1519214", "names": ["Secondary Glioblastoma", "Secondary Glioblastoma Multiforme"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary Glioblastoma", "shortest_name_length": 22}
{"curie": "UMLS:C1332506", "names": ["Benign Glomus Tumor", "Benign Glomus Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Glomus Tumor", "shortest_name_length": 19}
{"curie": "UMLS:C0030437", "names": ["Parakeratosis Variegata", "Parakeratosis variegata", "parakeratosis; variegata", "variegata; parakeratosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parakeratosis Variegata", "shortest_name_length": 23}
{"curie": "MONDO:0008563", "names": ["Piussan-Lenaerts-Mathieu syndrome", "Thumb ankylosis with mental retardation", "thumb stiff brachydactyly mental retardation", "Thumb ankylosis with intellectual disability", "thumb stiff brachydactyly intellectual disability", "thumb stiffness-brachydactyly-intellectual disability syndrome", "THUMBS, STIFF, WITH BRACHYDACTYLY TYPE A1 AND DEVELOPMENTAL DELAY", "Thumbs, Stiff, With Brachydactyly Type A1 And Developmental Delay", "thumbs, STIFF, with brachydactyly type A1 and developmental delay"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thumb stiffness-brachydactyly-intellectual disability syndrome", "shortest_name_length": 33}
{"curie": "MONDO:0001821", "names": ["Lack of erotic interest", "Lack or loss of sexual desire", "lack or loss of sexual desire", "Hypoactive Sexual Desire Disorder", "hypoactive sexual desire disorder", "Hypoactive sexual desire disorder", "Lack or loss of sexual desire (disorder)", "dysfunction; sexual, lack of sexual desire", "dysfunction; sexual, or loss of sexual desire", "hypoactive sexual desire disorder (diagnosis)", "sexual; functional disturbance, lack of sexual desire"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypoactive sexual desire disorder", "shortest_name_length": 23}
{"curie": "UMLS:C2903008", "names": ["enlarged prostate with lower urinary tract symptoms", "Enlarged Prostate with Lower Urinary Tract Symptoms", "enlarged prostate with lower urinary tract symptoms (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "enlarged prostate with lower urinary tract symptoms", "shortest_name_length": 51}
{"curie": "UMLS:C4525347", "names": ["Intrahepatic Cholangiocarcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intrahepatic Cholangiocarcinoma by AJCC v8 Stage", "shortest_name_length": 48}
{"curie": "MONDO:0005941", "names": ["retroperitoneal cancer", "Retroperitoneal cancer", "Tumor of retroperitoneum", "Retroperitoneal Neoplasm", "retroperitoneal neoplasm", "Retroperitoneal neoplasm", "tumor of retroperitoneum", "RETROPERITONEAL NEOPLASM", "Neoplasm, Retroperitoneal", "Tumour of retroperitoneum", "Retroperitoneal Neoplasms", "Neoplasms, Retroperitoneal", "Neoplasm of retroperitoneum", "neoplasm of retroperitoneum", "retroperitoneal space cancer", "neoplasm of the retroperitoneum", "Neoplasm of the retroperitoneum", "cancer of retroperitoneal space", "Malignant retroperitoneal tumor", "malignant retroperitoneal cancer", "Malignant retroperitoneal tumour", "Malignant Retroperitoneal Neoplasm", "malignant tumor of retroperitoneum", "malignant retroperitoneal neoplasm", "Malignant neoplasm of retroperitoneum", "malignant neoplasm of retroperitoneum", "Neoplasm of retroperitoneum (disorder)", "neoplasm of retroperitoneum (diagnosis)", "malignant retroperitoneal space neoplasm", "Malignant neoplasm of the retroperitoneum", "Malignant retroperitoneal tumor (disorder)", "malignant neoplasm of retroperitoneal space", "Malignant tumor of peritoneum and retroperitoneum", "malignant neoplasm of retroperitoneum (diagnosis)", "malignant tumor of peritoneum and retroperitoneum", "Malignant tumour of peritoneum and retroperitoneum", "malignant neoplasm of retroperitoneum and peritoneum", "Malignant neoplasm of retroperitoneum and peritoneum", "malignant neoplasm of peritoneum and retroperitoneum", "Malignant tumor of peritoneum and retroperitoneum (disorder)", "malignant neoplasm of peritoneum and retroperitoneum (diagnosis)", "Malignant neoplasm of malignant neoplasm of retroperitoneum and peritoneum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retroperitoneal cancer", "shortest_name_length": 22}
{"curie": "UMLS:C5418244", "names": ["Refractory Uterine Corpus Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Uterine Corpus Cancer", "shortest_name_length": 32}
{"curie": "MONDO:0018741", "names": ["TYLENOL TOXICITY", "tylenol toxicity", "toxicity tylenol", "paracetamol toxicity", "paracetamol poisoning", "Paracetamol poisoning", "acetaminophen toxicity", "toxicity acetaminophen", "ACETAMINOPHEN TOXICITY", "acetaminophen poisoning", "Acetaminophen poisoning", "Poisoning by paracetamol", "toxicity from paracetamol", "Poisoning by acetaminophen", "Acetaminophen intoxication", "toxicity from acetaminophen", "Poisoning caused by paracetamol", "paracetamol toxicity (diagnosis)", "Poisoning caused by acetaminophen", "acetaminophen toxicity (diagnosis)", "Poisoning caused by paracetamol (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paracetamol poisoning", "shortest_name_length": 16}
{"curie": "MONDO:0014684", "names": ["PNSED", "COXPD26", "combined oxidative phosphorylation deficiency 26", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 26", "Combined oxidative phosphorylation defect type 26", "combined oxidative phosphorylation defect type 26", "TRMT5 combined oxidative phosphorylation deficiency", "combined oxidative phosphorylation deficiency type 26", "COXPD26 - combined oxidative phosphorylation defect type 26", "Combined oxidative phosphorylation defect type 26 (disorder)", "combined oxidative phosphorylation deficiency caused by mutation in TRMT5", "PERIPHERAL NEUROPATHY WITH VARIABLE SPASTICITY, EXERCISE INTOLERANCE, AND DEVELOPMENTAL DELAY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation defect type 26", "shortest_name_length": 5}
{"curie": "UMLS:C5419158", "names": ["Endogenous Cushing Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endogenous Cushing Syndrome", "shortest_name_length": 27}
{"curie": "MONDO:0013349", "names": ["CDG1P", "CDG-Ip", "ALG11-CDG", "ALG11-CDG (CDG-Ip)", "CDG syndrome type Ip", "congenital disorder of glycosylation 1p", "congenital disorder of glycosylation Ip", "ALG11-congenital disorder of glycosylation", "Congenital disorder of glycosylation type Ip", "congenital disorder of glycosylation type 1p", "congenital disorder of glycosylation type Ip", "Congenital disorder of glycosylation type 1p", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip", "congenital disorder of glycosylation, type Ip", "Carbohydrate deficient glycoprotein syndrome type Ip", "carbohydrate deficient glycoprotein syndrome type Ip", "Congenital disorder of glycosylation type 1p (disorder)", "Congenital disorder of glycosylation type Ip (diagnosis)", "Asparagine-linked glycosylation 11 congenital disorder of glycosylation", "ALG11-CDG - asparagine-linked glycosylation 11 congenital disorder of glycosylation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ALG11-congenital disorder of glycosylation", "shortest_name_length": 5}
{"curie": "UMLS:C2828251", "names": ["stage IVA lip and oral cavity cancer", "Stage IVA Lip and Oral Cavity Cancer", "Stage IVA Lip and Oral Cavity Cancer AJCC v7", "Stage IVA Lip and Oral Cavity Cancer AJCC v6", "Stage IVA Lip and Oral Cavity Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Lip and Oral Cavity Cancer AJCC v6 and v7", "shortest_name_length": 36}
{"curie": "MONDO:0014899", "names": ["PEOB4", "autosomal recessive progressive external ophthalmoplegia 4", "PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE 4", "progressive external ophthalmoplegia, autosomal recessive 4", "adult-onset multiple mtDNA deletion syndrome due to DGUOK deficiency", "Adult-onset multiple mtDNA deletion syndrome due to DGUOK deficiency", "adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency", "Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency", "autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 4", "PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 4", "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4", "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive type 4", "Adult-onset multiple mitochondrial deoxyribonucleic acid deletion syndrome due to deoxyguanosine kinase deficiency", "Adult-onset multiple mitochondrial deoxyribonucleic acid deletion syndrome due to deoxyguanosine kinase deficiency (disorder)", "Adult-onset multiple mitochondrial DNA (deoxyribonucleic acid) deletion syndrome due to DGUOK (deoxyguanosine kinase) deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C5234872", "names": ["nasopharynx squamous cell carcinoma", "epidermoid carcinoma, nasopharyngeal", "nasopharyngeal squamous cell carcinoma", "squamous cell carcinoma, nasopharyngeal", "Keratinizing Epidermoid Carcinoma of Nasopharynx", "Nasopharyngeal Keratinizing Epidermoid Carcinoma", "Nasopharyngeal Keratinizing Squamous Cell Carcinoma", "Keratinizing Squamous Cell Carcinoma of Nasopharynx", "Keratinising squamous cell carcinoma of nasopharynx", "keratinizing squamous cell carcinoma of nasopharynx", "Keratinizing squamous cell carcinoma of nasopharynx", "Keratinizing Epidermoid Carcinoma of the Nasopharynx", "Keratinizing Squamous Cell Carcinoma of the Nasopharynx", "nasopharyngeal malignant carcinoma squamous cell keratinizing", "Keratinizing squamous cell carcinoma of nasopharynx (disorder)", "keratinizing squamous cell carcinoma of nasopharynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasopharyngeal Keratinizing Squamous Cell Carcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C1336232", "names": ["Stage IIIB Small Cell Lung Cancer without Pleural Effusion", "Stage IIIB Small Cell Cancer of Lung without Pleural Effusion", "Stage IIIB Small Cell Carcinoma of Lung without Pleural Effusion", "Stage IIIB Small Cell Cancer of the Lung without Pleural Effusion", "Stage IIIB Small Cell Carcinoma of the Lung without Pleural Effusion", "Stage IIIB Lung Small Cell Carcinoma without Pleural Effusion AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Lung Small Cell Carcinoma without Pleural Effusion AJCC v7", "shortest_name_length": 58}
{"curie": "UMLS:C4744854", "names": ["Genitourinary System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Genitourinary System Neoplasm", "shortest_name_length": 29}
{"curie": "UMLS:C0854143", "names": ["Relapsed Angiocentric Lymphoma", "Angiocentric lymphoma recurrent", "Recurrent Angiocentric Lymphoma", "Nasal T-cell lymphoma recurrent", "Polymorphic reticulosis recurrent", "Relapsed Nasal Type NK/T-Cell Lymphoma", "Recurrent Nasal Type Extranodal NK/T-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Angiocentric lymphoma recurrent", "shortest_name_length": 30}
{"curie": "UMLS:C4726600", "names": ["Undifferentiated Pelvic Pleomorphic Sarcoma", "Pelvic Undifferentiated High Grade Pleomorphic Sarcoma", "Undifferentiated High Grade Pleomorphic Sarcoma of the Pelvis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pelvic Undifferentiated High Grade Pleomorphic Sarcoma", "shortest_name_length": 43}
{"curie": "UMLS:C0558348", "names": ["Gastroenteritis bacterial", "Bacterial gastroenteritis", "Bacterial Gastroenteritis", "gastroenteritis bacterial", "bacterial gastroenteritis", "Gastroenteritis bacterial NOS", "bacterial intestinal infections", "Bacterial gastroenteritis (disorder)", "bacterial gastroenteritis (diagnosis)", "bacterial intestinal infections (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bacterial gastroenteritis", "shortest_name_length": 25}
{"curie": "UMLS:C1336552", "names": ["T-Cell Prolymphocytic Leukemia, Small Cell Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-Cell Prolymphocytic Leukemia, Small Cell Variant", "shortest_name_length": 50}
{"curie": "MONDO:0002870", "names": ["tr", "Tricuspid incompetence", "tricuspid incompetence", "Tricuspid Incompetence", "Incompetence;tricuspid", "tricuspid regurgitation", "Incompetence, Tricuspid", "incompetency; tricuspid", "tricuspid insufficiency", "TRICUSPID INSUFFICIENCY", "Tricuspid regurgitation", "Tricuspid Insufficiency", "Tricuspid insufficiency", "TRICUSPID REGURGITATION", "Tricuspid Regurgitation", "insufficiency, tricuspid", "regurgitation; tricuspid", "Regurgitation, Tricuspid", "insufficiency; tricuspid", "TI - Tricuspid incompetence", "Tricuspid valve incompetence", "TR - Tricuspid regurgitation", "Tricuspid Valve Incompetence", "Tricuspid regurgitation, NOS", "Tricuspid Valve Insufficiency", "Tricuspid valve insufficiency", "Tricuspid valve regurgitation", "tricuspid valve insufficiency", "Valve Incompetence, Tricuspid", "TRICUSPID VALVE REGURGITATION", "TRICUSPID VALVE INSUFFICIENCY", "Tricuspid Valve Regurgitation", "tricuspid valve regurgitation", "Incompetence, Tricuspid Valve", "TRICUSPID VALVE, REGURGITATION", "Insufficiency, Tricuspid Valve", "Regurgitation, Tricuspid Valve", "Valve Insufficiency, Tricuspid", "TRICUSPID VALVE, INSUFFICIENCY", "Valve Regurgitation, Tricuspid", "tricuspid (valve); incompetency", "tricuspid (valve); regurgitation", "Insufficiency of tricuspid valve", "tricuspid (valve); insufficiency", "Tricuspid valve incompetence, NOS", "Tricuspid valve insufficiency, NOS", "Tricuspid valve regurgitation, NOS", "tricuspid regurgitation (diagnosis)", "Tricuspid valve regurgitation (disorder)", "Right atrioventricular valve regurgitation", "Tricuspid Valve Insufficiency/ Regurgitation", "Regurgitation of right atrioventricular valve", "Right atrioventricular valve regurgitation (diagnosis)", "heart valve disorder atrioventricular right leaflet abnormality regurgitation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tricuspid valve insufficiency", "shortest_name_length": 2}
{"curie": "UMLS:C0858195", "names": ["MAC Lymphadenitis", "MAC lymphadenitis", "MAI Lymphadenitis", "MAI lymphadenitis", "Mycobacterium tuberculosis", "Mycobacterium Avium Complex Lymphadenitis", "Mycobacterium avium complex lymphadenitis", "Mycobacterium avium intracellulare lymphadenitis", "Mycobacterium Avium Intracellulare Lymphadenitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MAC lymphadenitis", "shortest_name_length": 17}
{"curie": "UMLS:C4520741", "names": ["stage III salivary gland cancer", "Stage III Salivary Gland Cancer", "Stage III Major Salivary Gland Cancer", "Stage III Major Salivary Gland Carcinoma", "Stage III Carcinoma of Major Salivary Gland", "Stage III Major Salivary Gland Cancer AJCC v7", "Stage III Carcinoma of the Major Salivary Gland", "Stage III Major Salivary Gland Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Major Salivary Gland Cancer AJCC v7", "shortest_name_length": 31}
{"curie": "MONDO:0020089", "names": ["Acquired lipodystrophy", "Lipodystrophy acquired", "acquired lipodystrophy", "acquired lipodystrophy (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired lipodystrophy", "shortest_name_length": 22}
{"curie": "UMLS:C1167866", "names": ["Renal Lymphocele", "Renal lymphocele", "Kidney Lymphocele"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal lymphocele", "shortest_name_length": 16}
{"curie": "MONDO:0020204", "names": ["Conjunctiva Tumor", "conjunctiva tumor", "conjunctiva tumors", "Conjunctival Tumor", "conjunctival tumor", "Conjunctiva--Tumors", "Tumor of conjunctiva", "tumor of conjunctiva", "Conjunctiva Neoplasm", "Tumor of Conjunctiva", "conjunctiva neoplasm", "conjunctival neoplasm", "Tumour of conjunctiva", "Conjunctival neoplasm", "Conjunctival Neoplasm", "conjunctival neoplasms", "Neoplasm, Conjunctival", "Conjunctival Neoplasms", "Neoplasm of Conjunctiva", "Neoplasms, Conjunctival", "neoplasm of conjunctiva", "Neoplasm of conjunctiva", "eye neoplasm conjunctiva", "tumor of the conjunctiva", "Tumor of the Conjunctiva", "Neoplasm of the Conjunctiva", "neoplasm of the conjunctiva", "conjunctiva neoplasm (disease)", "Neoplasm of conjunctiva (disorder)", "Neoplasm of conjunctiva (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "conjunctival tumor", "shortest_name_length": 17}
{"curie": "MONDO:0019516", "names": ["FEVR", "background retinopathy", "Retinopathy background", "Criswick-Schepens syndrome", "Background retinopathy, NOS", "exudative vitreoretinopathy", "Exudative vitreoretinopathy", "Unspecified background retinopathy", "Background retinopathy, unspecified", "Familial Exudative Vitreoretinopathy", "familial exudative vitreoretinopathy", "Familial exudative vitreoretinopathy", "exudative vitreoretinopathy, familial", "Exudative Vitreoretinopathy, Familial", "Vitreoretinopathy, Familial Exudative", "Familial Exudative Vitreoretinopathies", "FEVR - Familial exudative vitreoretinopathy", "[OBSOLETE] Familial Exudative Vitreoretinopathy", "Familial exudative vitreoretinopathy (disorder)", "familial exudative vitreoretinopathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exudative vitreoretinopathy", "shortest_name_length": 4}
{"curie": "MONDO:0019889", "names": ["trisomy 22qter", "Trisomy 22qter", "distal trisomy 22q", "Distal trisomy 22q", "distal duplication 22q", "Distal duplication 22q", "distal trisomy type 22q", "Telomeric duplication 22q", "telomeric duplication 22q", "partial trisomy 22q distal", "Distal trisomy 22q syndrome", "Distal trisomy 22q (diagnosis)", "Distal trisomy 22q syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal trisomy 22q", "shortest_name_length": 14}
{"curie": "UMLS:C5419875", "names": ["Pancreatic Neuroendocrine Tumor G3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Neuroendocrine Tumor G3", "shortest_name_length": 34}
{"curie": "MONDO:0024644", "names": ["ihd", "IHD", "ischemia; heart", "Cardiac ischemia", "cardiac ischemia", "cardiac ischaemia", "Cardiac ischaemia", "ISCHEMIA MYOCARDIAL", "Myocardial Ischemia", "Ischemia myocardial", "Myocardial ischemia", "MYOCARDIAL ISCHEMIA", "myocardial ischemia", "Ischemia, Myocardial", "Myocardial ischaemia", "ischemia; myocardial", "myocardium; ischemic", "myocardial Ischemias", "myocardial ischaemia", "Ischaemia myocardial", "Myocardial Ischemias", "ischemia, myocardial", "MYOCARDIAL ISCHAEMIA", "ischemias, myocardial", "Ischemias, Myocardial", "Ischemic heart disease", "ischemic heart disease", "Ischemic Heart Disease", "ISCHEMIC HEART DISEASE", "disease, ischemic heart", "ISCHEMIC HEART DISEASES", "Disease, Ischemic Heart", "heart disease, ischemic", "ischemic heart diseases", "Disease;ischaemic heart", "ischaemic heart disease", "Heart Disease, Ischemic", "Ischemic heart diseases", "Ischemic Heart Diseases", "HEART, ISCHEMIC DISEASE", "Ischaemic heart disease", "diseases, ischemic heart", "Heart Diseases, Ischemic", "heart diseases, ischemic", "Myocardial ischemia, NOS", "Ischaemic heart diseases", "Diseases, Ischemic Heart", "Myocardial ischaemia, NOS", "Ischemic heart disease NOS", "myocardium ischemic disease", "myocardial ischemia/hypoxia", "Ischemic heart disease, NOS", "Ischaemic heart disease, NOS", "IHD - Ischemic heart disease", "IHD - Ischaemic heart disease", "ischemic disease of myocardium", "Myocardial ischemia (disorder)", "myocardial ischemia (diagnosis)", "Ischemic heart diseases (I20-I25)", "Ischemic heart disease (disorder)", "ischemic heart disease (diagnosis)", "Ischemic heart disease or syndrome", "Ischemic Heart Diseases and Syndromes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myocardial ischemia", "shortest_name_length": 3}
{"curie": "UMLS:C3888435", "names": ["Product use issue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Product use issue", "shortest_name_length": 17}
{"curie": "MONDO:0012917", "names": ["SLI4", "Specific Language Impairment 4", "specific language impairment 4", "SPECIFIC LANGUAGE IMPAIRMENT 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "specific language impairment 4", "shortest_name_length": 4}
{"curie": "MONDO:0005771", "names": ["Annulus migrans", "erythema migran", "erythema migrans", "Geographic Tongue", "Tongue geographic", "TONGUE GEOGRAPHIC", "tongue geographic", "geographic tongue", "Geographic tongue", "LINGUA GEOGRAPHICA", "Tongue, Geographic", "Lingua geographica", "Pityriasis linguae", "TONGUE, GEOGRAPHIC", "lingua geographica", "Geographical tongue", "lingual geographica", "geographica; lingua", "Lingual geographica", "geographical tongue", "lingua; geographica", "Oral erythema migrans", "Psoriasiform mucositis", "Wandering rash of mouth", "wandering; rash, tongue", "rash; tongue, wandering", "Lingual Erythema Migrans", "Glossitis areata migrans", "Lingual erythema migrans", "erythema; migrans, tongue", "migrans; erythema, tongue", "Erythema Migrans, Lingual", "Denuded islands on tongue", "Benign migrating glossitis", "benign migratory glossitis", "Benign Migratory Glossitis", "Benign migratory glossitis", "migratory benign glossitis", "glossitis; benign migratory", "Migratory Glossitis, Benign", "Glossitis, Benign Migratory", "GLOSSITIS, BENIGN MIGRATORY", "Wandering rash of the tongue", "Glossitis Areata Exfoliativa", "Glossitis areata exfoliativa", "glossitis areata exfoliativa", "benign; glossitis, migratory", "Geographic tongue (disorder)", "geographic tongue (diagnosis)", "glossitis; exfoliativa areata", "exfoliativa areata; glossitis", "the tongue appeared geographic", "geographic tongue (physical finding)", "glossitis areata exfoliativa (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "geographic tongue", "shortest_name_length": 15}
{"curie": "MONDO:0020747", "names": ["STSL1", "SITOSTEROLEMIA 1", "sitosterolemia 1", "Macrothrombocytopenia-Stomatocytosis, Mediterranean", "MACROTHROMBOCYTOPENIA/STOMATOCYTOSIS, MEDITERRANEAN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sitosterolemia 1", "shortest_name_length": 5}
{"curie": "UMLS:C1710630", "names": ["Ventricular Perforation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ventricular Perforation", "shortest_name_length": 23}
{"curie": "UMLS:C0347634", "names": ["spleen hematoma", "splenic hematoma", "Splenic hematoma", "Splenic haematoma", "hematoma of spleen", "Hematoma of spleen", "Haematoma of spleen", "Splenic hematoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Splenic hematoma", "shortest_name_length": 15}
{"curie": "MONDO:0015629", "names": ["VWD2B", "Von Willebrand disease type 2B", "Type 2B von Willebrand Disease", "von Willebrand disease type 2B", "Type IIB von Willebrand Disease", "von Willebrand Disease, Type 2B", "Von Willebrand disease, type 2B", "VON WILLEBRAND DISEASE, TYPE 2B", "von Willebrand disease, type 2B", "von Willebrand disease, type IIB", "von Willebrand Disease, Type IIB", "Hereditary von Willebrand disease type 2B", "von Willebrand disease type 2B (diagnosis)", "Hereditary von Willebrand disease type 2B (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "von Willebrand disease type 2B", "shortest_name_length": 5}
{"curie": "MONDO:0008471", "names": ["SEDC", "SED CONGENITA", "SED Congenita", "SED congenita", "Sed, Congenital Type", "Spranger-Wiedemann disease", "Spondyloepiphyseal dysplasia", "spondyloepiphyseal; dysplasia", "dysplasia; spondyloepiphyseal", "Late Spondyloepiphyseal Dysplasia", "Spondyloepiphyseal dysplasia, NOS", "SED - Spondyloepiphyseal dysplasia", "SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA", "spondyloepiphyseal dysplasia congenita", "Spondyloepiphyseal dysplasia congenita", "Spondyloepiphyseal Dysplasia Congenita", "Congenital spondyloepiphyseal dysplasia", "Spondyloepiphyseal dysplasia, congenita", "congenital spondyloepiphyseal dysplasia", "Spondyloepiphyseal dysplasia congenita group", "Spondyloepiphyseal dysplasia, congenital type", "spondyloepiphyseal dysplasia, congenital type", "SEDC - Spondyloepiphyseal dysplasia congenita", "SPONDYLOEPIPHYSEAL DYSPLASIA, CONGENITAL TYPE", "Spondyloepiphyseal dysplasia congenita syndrome", "Spondyloepiphyseal dysplasia congenita group (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepiphyseal dysplasia congenita", "shortest_name_length": 4}
{"curie": "MONDO:0010402", "names": ["MRX94", "MRXSW", "MRXS29", "mental retardation, X-linked 94", "Mental Retardation, X-Linked 94", "MENTAL RETARDATION, X-LINKED 94", "intellectual disability, X-linked 94", "syndromic X-linked mental retardation 29", "MENTAL RETARDATION, X-LINKED, SYNDROMIC 29", "mental retardation, X-linked, syndromic 29", "syndromic X-linked mental retardation Wu type", "syndromic X-linked intellectual disability 94", "syndromic X-linked intellectual disability 29", "intellectual disability, X-linked, syndromic 29", "mental retardation, X-linked, syndromic, Wu type", "syndromic X-linked intellectual disability type 94", "syndromic X-linked intellectual disability Wu type", "intellectual disability, X-linked, syndromic, Wu type", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, WU TYPE", "syndromic X-linked intellectual disability due to GRIA3 anomalies", "intellectual developmental disorder, X-linked, syndromic, Wu type, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic X-linked intellectual disability 94", "shortest_name_length": 5}
{"curie": "MONDO:0700172", "names": ["horse lymphoma", "Horse Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "horse lymphoma", "shortest_name_length": 14}
{"curie": "MONDO:0032819", "names": ["CHNG7", "TRH resistance syndrome", "congenital nongoitrous hypothyroidism 7", "HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 7", "hypothyroidism, congenital, nongoitrous, 7", "Resistance to thyrotropin-releasing hormone syndrome", "resistance to thyrotropin-releasing hormone syndrome", "Thyrotropin-Releasing Hormone Resistance, Generalized", "thyrotropin-releasing hormone resistance, generalized", "Central hypothyroidism due to TRH receptor deficiency", "central hypothyroidism due to TRH receptor deficiency", "THYROTROPIN-RELEASING HORMONE RESISTANCE, GENERALIZED", "TRH (thyrotropin-releasing hormone) resistance syndrome", "Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency", "Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypothyroidism, congenital, nongoitrous, 7", "shortest_name_length": 5}
{"curie": "MONDO:0011321", "names": ["Expansile Bone Lesions", "EXPANSILE BONE LESIONS", "expansile bone lesions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "expansile bone lesions", "shortest_name_length": 22}
{"curie": "MONDO:0003191", "names": ["Rete Ovarii Adenocarcinoma", "rete ovarii adenocarcinoma", "Adenocarcinoma of rete ovarii", "Adenocarcinoma of rete ovarii (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rete ovarii adenocarcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0002101", "names": ["facial nerve tumor", "Facial Nerve Tumor", "facial nerve tumors", "Facial Nerve Tumors", "tumor of Facial nerve", "Facial Nerve Neoplasm", "tumor of facial nerve", "facial nerve neoplasm", "Tumor of Facial Nerve", "facial nerve neoplasms", "Facial Nerve Neoplasms", "neoplasm of Facial nerve", "Neoplasm of Facial Nerve", "Neoplasm of facial nerve", "neoplasm of facial nerve", "tumor of the Facial nerve", "Tumor of the Facial Nerve", "VIIth Cranial Nerve Tumors", "VIIth cranial nerve tumors", "seventh cranial nerve tumor", "Seventh Cranial Nerve Tumor", "neoplasm of the Facial nerve", "Seventh Cranial Nerve Tumors", "seventh cranial nerve tumors", "Neoplasm of the Facial Nerve", "VIIth cranial nerve neoplasms", "VIIth Cranial Nerve Neoplasms", "seventh cranial nerve neoplasm", "tumor of seventh cranial nerve", "Tumor of Seventh Cranial Nerve", "Seventh Cranial Nerve Neoplasm", "Seventh Cranial Nerve Neoplasms", "facial nerve neoplasm (disease)", "seventh cranial nerve neoplasms", "Neoplasm of Seventh Cranial Nerve", "neoplasm of seventh cranial nerve", "Tumor of the Seventh Cranial Nerve", "tumor of the seventh cranial nerve", "Neoplasm of facial nerve (disorder)", "neoplasm of the seventh cranial nerve", "Neoplasm of the Seventh Cranial Nerve", "neoplasm of seventh cranial nerve (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "facial nerve neoplasm", "shortest_name_length": 18}
{"curie": "MONDO:0054846", "names": ["FAME6", "FCMTE6", "BAFME6", "familial adult myoclonic epilepsy 6", "EPILEPSY, FAMILIAL ADULT MYOCLONIC, 6", "epilepsy, familial adult myoclonic, 6", "epilepsy, FAMILIAL ADULT myoclonic, 6", "benign Adult Familial myoclonic epilepsy 6", "benign adult familial myoclonic epilepsy 6", "BENIGN ADULT FAMILIAL MYOCLONIC EPILEPSY 6", "familial cortical myoclonic tremor and epilepsy 6", "cortical myoclonic tremor with epilepsy, Familial, 6", "CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, familial adult myoclonic, 6", "shortest_name_length": 5}
{"curie": "MONDO:0004680", "names": ["Primary thrombocytopenia", "primary thrombocytopenia", "primary; thrombocytopenia", "thrombocytopenia; primary", "primary thrombocytopenias", "Primary thrombocytopenia NOS", "Other primary thrombocytopenia", "Primary thrombocytopenia (disorder)", "primary thrombocytopenia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary thrombocytopenia", "shortest_name_length": 24}
{"curie": "MONDO:0003431", "names": ["adenolipoma", "Lipoadenoma", "lipoadenoma", "Adenolipoma", "adenolipoma, benign", "ADENOLIPOMA, BENIGN", "lipoadenoma (morphologic abnormality)", "Lipoadenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lipoadenoma", "shortest_name_length": 11}
{"curie": "MONDO:0002671", "names": ["SRC breast carcinoma", "SRC Breast Carcinoma", "SRC carcinoma of breast", "SRC Carcinoma of Breast", "SRC carcinoma of the breast", "SRC Carcinoma of the Breast", "primary SRC breast carcinoma", "Primary SRC Breast Carcinoma", "Primary SRC Carcinoma of Breast", "primary SRC carcinoma of breast", "signet ring cell breast carcinoma", "Breast Signet Ring Cell Carcinoma", "Signet Ring Cell Breast Carcinoma", "breast carcinoma with signet ring", "Breast Signet-Ring Cell Carcinoma", "breast signet ring cell carcinoma", "signet Ring cell breast carcinoma", "mammary signet Ring cell carcinoma", "Mammary Signet Ring cell carcinoma", "Mammary Signet Ring Cell Carcinoma", "primary SRC carcinoma of the breast", "Primary SRC Carcinoma of the Breast", "Signet Ring Cell Carcinoma of Breast", "signet ring cell carcinoma of breast", "signet Ring cell carcinoma of breast", "breast signet ring cell adenocarcinoma", "Signet Ring Cell Carcinoma of the Breast", "signet Ring cell carcinoma of the breast", "Primary Signet Ring Cell Breast Carcinoma", "primary signet Ring cell breast carcinoma", "Primary Mammary Signet Ring Cell Carcinoma", "primary mammary signet Ring cell carcinoma", "Primary Signet Ring Cell Carcinoma of Breast", "primary signet Ring cell carcinoma of breast", "primary signet Ring cell carcinoma of the breast", "Primary Signet Ring Cell Carcinoma of the Breast", "signet ring cell carcinoma of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "signet ring cell breast carcinoma", "shortest_name_length": 20}
{"curie": "MONDO:0019971", "names": ["melanoma of soft tissue", "clear cell sarcoma of the tendons and aponeuroses"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melanoma of soft tissue", "shortest_name_length": 23}
{"curie": "MONDO:0016371", "names": ["combined hyperactive dysfunction syndrome of the cranial nerves"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined hyperactive dysfunction syndrome of the cranial nerves", "shortest_name_length": 63}
{"curie": "MONDO:0100210", "names": ["growth hormone insensitivity syndrome with immune dysregulation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "growth hormone insensitivity syndrome with immune dysregulation", "shortest_name_length": 63}
{"curie": "MONDO:0012468", "names": ["rhizomelic dysplasia, scoliosis, and retinitis pigmentosa", "RHIZOMELIC DYSPLASIA, SCOLIOSIS, AND RETINITIS PIGMENTOSA", "Rhizomelic dysplasia, scoliosis, and retinitis pigmentosa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rhizomelic dysplasia, scoliosis, and retinitis pigmentosa", "shortest_name_length": 57}
{"curie": "MONDO:0017348", "names": ["lymphoepithelial-like carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphoepithelial-like carcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C1336175", "names": ["Stage IIB Adenosquamous Lung Cancer", "Stage IIB Adenosquamous Lung Carcinoma", "Stage IIB Adenosquamous Cell Lung Carcinoma", "Stage IIB Adenosquamous Cell Carcinoma of Lung", "Stage IIB Lung Adenosquamous Carcinoma AJCC v7", "Stage IIB Adenosquamous Cell Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Lung Adenosquamous Carcinoma AJCC v7", "shortest_name_length": 35}
{"curie": "UMLS:C0854835", "names": ["Stage I Angioimmunoblastic T-Cell Lymphoma", "Angioimmunoblastic T-Cell Lymphoma Stage I", "Angioimmunoblastic T-cell lymphoma stage I", "Ann Arbor Stage I Angioimmunoblastic T-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Angioimmunoblastic T-cell lymphoma stage I", "shortest_name_length": 42}
{"curie": "UMLS:C2982461", "names": ["Stage III Oropharyngeal Carcinoma", "Stage III Oropharyngeal Throat Cancer", "Stage III Oropharyngeal Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Oropharyngeal Carcinoma AJCC v7", "shortest_name_length": 33}
{"curie": "MONDO:0019976", "names": ["Boxer's dementia", "dementia pugilistica", "punch-drunk syndrome", "Chronic Brain Injury", "chronic brain injury", "Brain Injury, Chronic", "Chronic Brain Injuries", "Brain Injuries, Chronic", "chronic traumatic encephalopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dementia pugilistica", "shortest_name_length": 16}
{"curie": "MONDO:0013109", "names": ["ALL2", "LEUKEMIA, ACUTE LYMPHOCYTIC, SUSCEPTIBILITY TO, 2", "leukemia, acute lymphocytic, susceptibility to, 2", "leukemia, acute lymphoblastic, susceptibility to, 2", "LEUKEMIA, ACUTE LYMPHOBLASTIC, SUSCEPTIBILITY TO, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukemia, acute lymphocytic, susceptibility to, 2", "shortest_name_length": 4}
{"curie": "MONDO:0013111", "names": ["LFIT", "TRMU infantile liver failure", "acute infantile liver failure", "transient infantile liver failure", "liver failure, transient infantile", "liver failure, infantile, transient", "LIVER FAILURE, INFANTILE, TRANSIENT", "infantile liver failure caused by mutation in TRMU", "acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins", "acute infantile liver failure due to synthesis defect of mitochondrial DNA-encoded proteins"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins", "shortest_name_length": 4}
{"curie": "UMLS:C1709869", "names": ["Rectosigmoid Signet-Ring Cell Carcinoma", "Rectosigmoid Signet Ring Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rectosigmoid Signet Ring Cell Carcinoma", "shortest_name_length": 39}
{"curie": "UMLS:C4289806", "names": ["Cesarean Scar Pregnancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cesarean Scar Pregnancy", "shortest_name_length": 23}
{"curie": "MONDO:0007722", "names": ["heterochromia", "Heterochromic iris", "Heterochromia irides", "heterochromia iridis", "Heterochromia iridis", "HETEROCHROMIA IRIDIS", "Different colored eyes", "Different coloured eyes", "Heterochromic iris (finding)", "heterochromia iridis (disease)", "Asymmetry of iris pigmentation", "Asymmetry in the pigmentation of the irides", "Pigmentary abnormality of the anterior segment of the eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heterochromia iridis", "shortest_name_length": 13}
{"curie": "UMLS:C0007370", "names": ["CATALEPSY", "catalepsy", "Catalepsy", "Anochlesia", "Anochlesias", "Catalepsies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Catalepsy", "shortest_name_length": 9}
{"curie": "MONDO:0100120", "names": ["Vectorborne Disease", "Vectorborne Diseases", "Vector-Borne Disease", "vector-borne disease", "Vector-borne disease", "Vector Borne Disease", "Vector-Borne Diseases", "Vector Borne Diseases", "vector-borne infection", "Vector-transmitted disease", "Vector-borne infectious disease", "vector-borne infectious disease", "Vector-transmitted infectious disease", "Vector-transmitted infectious disease (navigational concept)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vector-borne disease", "shortest_name_length": 19}
{"curie": "MONDO:0010852", "names": ["CHROMOSOME 8q12.1-q21.2 DELETION SYNDROME", "chromosome 8Q12.1-q21.2 deletion syndrome", "bor-Duane hydrocephalus contiguous Gene syndrome", "BOR-DUANE HYDROCEPHALUS CONTIGUOUS GENE SYNDROME", "Bor-Duane hydrocephalus contiguous gene syndrome", "Branchio-Oto-renal Duane hydrocephalus contiguous gene syndrome", "Branchio-Oto-Renal Duane hydrocephalus contiguous gene syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 8Q12.1-q21.2 deletion syndrome", "shortest_name_length": 41}
{"curie": "MONDO:0001926", "names": ["Ureter Disease", "ureter disease", "ureter disorder", "Ureter Disorder", "Ureteric Disease", "ureter; disorder", "ureteric disease", "Ureteral Disease", "disorders ureter", "ureteral disease", "ureteral disorder", "Ureters--Diseases", "Ureteric Disorder", "Ureteral disorder", "Disease, Ureteral", "ureteric disorder", "Ureteral Diseases", "disease of ureter", "disorder of ureter", "Diseases, Ureteral", "Ureteral Disorders", "Ureteric disorders", "Disorder of ureter", "Ureteral disorder NOS", "ureter disease or disorder", "Ureteral disease or syndrome", "Disorder of ureter (disorder)", "disease (or disorder); ureter", "disease or disorder of ureter", "disorder of ureter (diagnosis)", "Ureteral Diseases and Syndromes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ureteral disorder", "shortest_name_length": 14}
{"curie": "MONDO:0014625", "names": ["DEE33", "EIEE33", "early infantile epileptic encephalopathy 33", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 33", "epileptic encephalopathy, early infantile, 33", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 33", "developmental and epileptic encephalopathy 33", "developmental and epileptic encephalopathy, 33", "EEF1A2 early infantile epileptic encephalopathy", "epileptic encephalopathy, early infantile, type 33", "early infantile epileptic encephalopathy caused by mutation in EEF1A2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 33", "shortest_name_length": 5}
{"curie": "MONDO:0016583", "names": ["Stalker-Chitayat syndrome", "Stalker Chitayat syndrome", "intestinal malrotation facial anomalies familial type", "familial intestinal malrotation-facial anomalies syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial intestinal malrotation-facial anomalies syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0024559", "names": ["AAT1", "FAA1", "Familial Taad", "Annuloaortic Ectasia", "ANNULOAORTIC ECTASIA", "Annuloaortic ectasia", "annuloaortic ectasia", "annulo aortic ectasia", "Annulo-aortic ectasia", "Familial Aortic Aneurysm", "aneurysm, thoracic aortic", "Familial aortic dissection", "Familial Aortic Dissection", "Aortic Dissection, Familial", "aortic dissection, familial", "AORTIC DISSECTION, FAMILIAL", "Cystic medial necrosis of aorta", "annuloaortic ectasia (diagnosis)", "Familial Thoracic Aortic Aneurysm", "thoracic aortic aneurysm, familial", "Aortic Aneurysm, Familial Thoracic", "AORTIC ANEURYSM, FAMILIAL THORACIC", "aortic aneurysm, familial thoracic", "Aortic Aneurysm, Familial Thoracic 1", "aortic aneurysm, familial thoracic 1", "AORTIC ANEURYSM, FAMILIAL THORACIC 1", "Congenital aneurysm of ascending aorta", "Erdheim cystic medial necrosis of aorta", "thoracic aortic aneurysm, familial (diagnosis)", "Familial Thoracic Aortic Aneurysm and Dissection", "Congenital aneurysm of ascending aorta (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic aneurysm, familial thoracic 1", "shortest_name_length": 4}
{"curie": "MONDO:0012756", "names": ["AUTS14A", "Del(16)(p11.2)", "monosomy 16p11.2", "microdeletion 16p11.2", "proximal del(16)(p11.2)", "Proximal del(16)(p11.2)", "Proximal monosomy 16p11.2", "16p11.2 Deletion Syndrome", "16p11.2 deletion syndrome", "autism susceptibility 14A", "proximal monosomy 16p11.2", "autism, susceptibility to, 14A", "AUTISM, SUSCEPTIBILITY TO, 14A", "chromosome 16p11.2 deletion syndrome", "Chromosome 16p11.2 deletion syndrome", "Chromosome 16p11.2 Deletion Syndrome", "proximal 16p11.2 microdeletion syndrome", "Proximal 16p11.2 microdeletion syndrome", "chromosome 16p11.2 deletion syndrome, 593kb", "CHROMOSOME 16p11.2 DELETION SYNDROME, 593-KB", "chromosome 16p11.2 deletion syndrome, 593-KB", "Chromosome 16p11.2 deletion syndrome (disorder)", "Proximal 16p11.2 microdeletion syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "proximal 16p11.2 microdeletion syndrome", "shortest_name_length": 7}
{"curie": "MONDO:0004352", "names": ["brain ependymoma", "Brain Ependymoma", "adult brain ependymoma", "Adult Brain Ependymoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult brain ependymoma", "shortest_name_length": 16}
{"curie": "MONDO:0019233", "names": ["disorder of peroxisomal beta oxidation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of peroxisomal beta oxidation", "shortest_name_length": 38}
{"curie": "MONDO:0021678", "names": ["Gram-negative bacilli; infection", "infection; gram-negative bacilli", "Gram-negative bacteria infection", "Gram-Negative Bacterial Infection", "gram-negative bacterial infection", "Bacterial Infection, Gram-Negative", "infection, gram-negative bacterial", "Gram Negative Bacterial Infections", "Gram-Negative Bacterial Infections", "Infection, Gram-Negative Bacterial", "Gram-negative bacterial infections", "gram-negative bacterial infections", "bacterial infection, gram-negative", "gram negative bacterial infections", "infections, gram-negative bacterial", "bacterial infections, gram negative", "Infections, Gram-Negative Bacterial", "Bacterial Infections, Gram-Negative", "bacterial infections, gram-negative", "infections, gram negative bacterial", "Gram-negative bacterial infection NOS", "Disease due to Gram-negative bacteria", "Disease caused by Gram-negative bacteria", "Gram-negative bacteria infection (diagnosis)", "Bacterial infection with gram-negative bacteria NOS", "Disease caused by Gram-negative bacteria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gram-negative bacterial infections", "shortest_name_length": 32}
{"curie": "UMLS:C0262395", "names": ["borderline bp", "borderline htn", "BORDERLINE HYPERTENSION", "Borderline hypertension", "hypertension borderline", "Borderline Hypertension", "borderline hypertension", "hypertension; borderline", "borderline; hypertension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline hypertension", "shortest_name_length": 13}
{"curie": "MONDO:0014365", "names": ["SPGF13", "TAF4B azoospermia", "spermatogenic failure 13", "SPERMATOGENIC FAILURE 13", "spermatogenic failure type 13", "azoospermia caused by mutation in TAF4B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 13", "shortest_name_length": 6}
{"curie": "MONDO:0007175", "names": ["PR interval, variation in", "PR INTERVAL, VARIATION IN", "PR interval, variation type in", "Atrioventricular conduction time, variation in", "ATRIOVENTRICULAR CONDUCTION TIME, VARIATION IN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PR interval, variation in", "shortest_name_length": 25}
{"curie": "UMLS:C0854980", "names": ["Large cell lung cancer stage II", "Stage II Large Cell Lung Cancer", "Stage II Large Cell Lung Carcinoma", "Stage II Large Cell Carcinoma of Lung", "Stage II Large Cell Carcinoma of the Lung", "Stage II Lung Large Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Large cell lung cancer stage II", "shortest_name_length": 31}
{"curie": "MONDO:0005737", "names": ["EHF", "Ebola", "Ebola fever", "disease ebola", "Ebola disease", "Ebola Infection", "Infection, Ebola", "Ebola virus disease", "ebola virus disease", "Ebola Virus Disease", "Ebolavirus Infection", "Ebola virus infection", "Ebola Virus Infection", "Infection, Ebolavirus", "ebola virus infection", "Ebolavirus Infections", "Infections, Ebolavirus", "Virus Infection, Ebola", "Infection, Ebola Virus", "Ebola hemorrhagic fever", "Ebola Hemorrhagic Fever", "ebola fever hemorrhagic", "ebola hemorrhagic fever", "Ebola haemorrhagic fever", "ebola haemorrhagic fever", "Hemorrhagic Fever, Ebola", "EVD - Ebola virus disease", "Ebolavirus infectious disease", "Ebola virus hemorrhagic fever", "Viral hemorrhagic fever, Ebola", "Ebola virus disease (disorder)", "Ebolavirus disease or disorder", "Viral haemorrhagic fever, Ebola", "Ebolavirus caused disease or disorder", "Ebola virus hemorrhagic fever (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ebola hemorrhagic fever", "shortest_name_length": 3}
{"curie": "UMLS:C0856069", "names": ["Vasculitis gastrointestinal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vasculitis gastrointestinal", "shortest_name_length": 27}
{"curie": "MONDO:0015667", "names": ["AML, NOS", "unclassified AML", "acute myeloid leukemia", "Acute myeloid leukemia", "Acute Myeloid Leukemia NOS", "acute myeloid leukemia NOS", "Acute myeloid leukemia, NOS", "Acute Myeloid Leukemia, NOS", "AML not otherwise specified", "acute myeloid leukemia, NOS", "AML, Not Otherwise Specified", "unclassified acute myeloid leukemia", "acute myeloid leukemia by FAB classification", "acute myeloid leukemia not otherwise specified", "Acute Myeloid Leukemia Not Otherwise Specified", "acute myeloid leukemia not otherwise categorized", "Acute Myeloid Leukemia Not Otherwise Categorized"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia by FAB classification", "shortest_name_length": 8}
{"curie": "UMLS:C4525397", "names": ["I", "Stage I Distal Bile Duct Cancer AJCC v8", "Stage I Distal Bile Duct Carcinoma AJCC v8", "Stage I Extrahepatic (Distal) Bile Duct Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Distal Bile Duct Cancer AJCC v8", "shortest_name_length": 1}
{"curie": "MONDO:0007392", "names": ["COXOAURICULAR SYNDROME", "Coxoauricular syndrome", "coxoauricular syndrome", "Coxoauricular Syndrome", "Coxoauricular syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coxoauricular syndrome", "shortest_name_length": 22}
{"curie": "MONDO:0003421", "names": ["Mixed Cell Adenoma", "Mixed cell adenoma", "mixed cell adenoma", "Mixed cell adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed cell adenoma", "shortest_name_length": 18}
{"curie": "MONDO:0014364", "names": ["MC3DN8", "LYRM7 mitochondrial complex III deficiency", "mitochondrial Complex 3 deficiency, nuclear type 8", "mitochondrial complex III deficiency nuclear type 8", "MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8", "mitochondrial complex III deficiency, nuclear type 8", "mitochondrial complex III deficiency caused by mutation in LYRM7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex III deficiency nuclear type 8", "shortest_name_length": 6}
{"curie": "UMLS:C1335004", "names": ["Non-Neoplastic Corneal Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Corneal Disorder", "shortest_name_length": 31}
{"curie": "MONDO:0022070", "names": ["Cantu sanchez-corona hernandez syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cantu sanchez-corona hernandez syndrome", "shortest_name_length": 39}
{"curie": "MONDO:0001894", "names": ["Spinal Cord Sarcoma", "spinal cord sarcoma", "sarcoma of spinal cord", "Sarcoma of Spinal Cord", "sarcoma of the Spinal Cord", "Sarcoma of the Spinal Cord", "sarcoma of the spinal cord", "sarcoma of spinal cord (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal cord sarcoma", "shortest_name_length": 19}
{"curie": "UMLS:C4761243", "names": ["Complete neonatal hearing loss", "Complete Neonatal Hearing Loss"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Complete neonatal hearing loss", "shortest_name_length": 30}
{"curie": "MONDO:0010474", "names": ["APLCC", "LSDMCA2", "COX7B microphthalmia with linear skin defects syndrome", "linear skin defects with multiple congenital anomalies 2", "LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2", "linear skin defects with multiple congenital anomalies type 2", "linear skin defects with multiple congenital anomalies 2, X-linked dominant", "microphthalmia with linear skin defects syndrome caused by mutation in COX7B", "aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies", "APLASIA CUTIS CONGENITA, RETICULOLINEAR, WITH MICROCEPHALY, FACIAL DYSMORPHISM, AND OTHER CONGENITAL ANOMALIES", "aplasia cutis congenita, Reticulolinear, with microcephaly, Facial Dysmorphism, and Other congenital anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "linear skin defects with multiple congenital anomalies 2", "shortest_name_length": 5}
{"curie": "MONDO:0030947", "names": ["CONRIBA", "CLCN6-related childhood-onset progressive neurodegeneration-peripheral neuropathy syndrome", "neurodegeneration, childhood-onset, hypotonia, respiratory insufficiency and brain imaging abnormalities", "neurodegeneration, childhood-onset, with hypotonia, respiratory insufficiency, and brain imaging abnormalities", "NEURODEGENERATION, CHILDHOOD-ONSET, WITH HYPOTONIA, RESPIRATORY INSUFFICIENCY, AND BRAIN IMAGING ABNORMALITIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodegeneration, childhood-onset, with hypotonia, respiratory insufficiency, and brain imaging abnormalities", "shortest_name_length": 7}
{"curie": "MONDO:0004212", "names": ["vulvar keratoacanthoma", "Vulvar Keratoacanthoma", "vulvar keratoacanthoma-like carcinoma", "Vulvar Keratoacanthoma-Like Carcinoma", "vulvar squamous cell carcinoma, keratoacanthoma type", "Vulvar Squamous Cell Carcinoma, Keratoacanthoma Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar keratoacanthoma-like carcinoma", "shortest_name_length": 22}
{"curie": "MONDO:0003319", "names": ["scrotal Ca", "Scrotal Ca", "Scrotal Tumor", "scrotum tumor", "tumor scrotum", "Scrotal tumor", "scrotal tumor", "Scrotum tumor", "Scrotum tumour", "scrotum cancer", "scrotal neoplasm", "Tumor of Scrotum", "Tumor of scrotum", "Scrotal Neoplasm", "tumor of scrotum", "scrotum neoplasm", "Scrotal neoplasms", "Tumour of scrotum", "Neoplasm of Scrotum", "neoplasm of scrotum", "Neoplasm of scrotum", "Tumor of the Scrotum", "tumor of the scrotum", "Neoplasm of the Scrotum", "neoplasm of the scrotum", "Neoplasm of the scrotum", "Neoplasia of the scrotum", "malignant scrotal neoplasm", "scrotum neoplasm (disease)", "malignant tumor of scrotum", "malignant Scrotal neoplasm", "malignant tumour of scrotum", "Neoplasm of scrotum (disorder)", "neoplasm of scrotum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scrotum neoplasm", "shortest_name_length": 10}
{"curie": "MONDO:0000171", "names": ["WWS", "HARD SYNDROME", "HARD Syndrome", "HARD syndrome", "hard syndrome", "Syndrome, HARD", "Pagon syndrome", "HARD Syndromes", "Pagon Syndrome", "COD MD Syndrome", "Hard E syndrome", "Chemke Syndrome", "Syndrome, Pagon", "Pagon Syndromes", "Chemke syndrome", "COD-MD Syndrome", "COD-MD SYNDROME", "Warburg syndrome", "COD-MD Syndromes", "Warburg Syndrome", "warburg syndrome", "Syndrome, COD-MD", "Syndrome, Chemke", "syndrome warburgs", "Syndrome, Warburg", "hard +/- E syndrome", "Walker-Warburg syndrome", "walker warburg syndrome", "syndrome walker warburg", "Walker Warburg Syndrome", "walker-warburg syndrome", "Walker Warburg syndrome", "Walker-Warburg Syndrome", "Syndrome, Walker-Warburg", "cerebroocular dysgenesis", "cerebro-ocular dysgenesis", "Walker lissencephaly syndrome", "Walker-Warburg syndrome (WWS)", "cerebro-ocular dysgenesis (COD)", "Walker-Warburg muscular dystrophy", "Walker-Warburg Muscular Dystrophy", "congenital encephalo-ophthalmic dysplasia", "Hydrocephalus, agyria and retinal dysplasia", "hydrocephalus, agyria and retinal dysplasia", "cerebro-ocular dysplasia-muscular dystrophy", "Walker-Warburg congenital muscular dystrophy", "Hydrocephalus, Agyria, And Retinal Dysplasia", "HYDROCEPHALUS, AGYRIA, AND RETINAL DYSPLASIA", "muscular dystrophy-dystroglycanopathy, type A", "Hydrocephalus-agyria-retinal dysplasia syndrome", "hydrocephalus-agyria-retinal dysplasia syndrome", "HARD - Hydrocephalus, agyria and retinal dysplasia", "Cerebroocular Dysplasia Muscular Dystrophy Syndrome", "cerebroocular dysplasia muscular dystrophy syndrome", "Cerebroocular Dysplasia-Muscular Dystrophy Syndrome", "CEREBROOCULAR DYSPLASIA-MUSCULAR DYSTROPHY SYNDROME", "cerebroocular dysplasia-muscular dystrophy syndrome", "cerebro-ocular dysgenesis-muscular dystrophy syndrome", "Walker-Warburg congenital muscular dystrophy (disorder)", "HARD (hydrocephalus, agyria, retinal dysplasia) syndrome", "cerebro-ocular dysgenesis-muscular dystrophy (COD-MD) syndrome", "hydrocephalus, agyria, retinal dysplasia with or without encephalocele syndrome", "hydrocephalus, agyria, retinal dysplasia with or without encephalocele (HARD+/-E) syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy-dystroglycanopathy, type A", "shortest_name_length": 3}
{"curie": "UMLS:C1262242", "names": ["Stomal hernia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stomal hernia", "shortest_name_length": 13}
{"curie": "UMLS:C0036346", "names": ["children schizophrenia", "schizophrenia children", "Childhood Schizophrenia", "Schizophrenia childhood", "Childhood schizophrenia", "schizophrenia childhood", "childhood schizophrenia", "Schizophrenia, Childhood", "Schizophrenia in children", "schizophrenia in children", "Childhood Onset Schizophrenia", "schizophrenia; childhood type", "Childhood-Onset Schizophrenia", "Schizophrenia, childhood type", "childhood type; schizophrenic", "Schizophrenia, Childhood-Onset", "Schizophrenia, childhood type NOS", "Schizophrenic syndrome of childhood", "childhood schizophrenia (diagnosis)", "syndrome; schizophrenic of childhood", "schizophrenia; syndrome of childhood", "Schizophrenic syndrome of childhood NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Schizophrenia, Childhood", "shortest_name_length": 22}
{"curie": "MONDO:0004485", "names": ["interstitial myocarditis", "Interstitial Myocarditis", "MYOCARDITIS INTERSTITIAL", "Interstitial myocarditis", "Myocarditis interstitial", "Myocarditis, interstitial", "Interstitial myocarditis, NOS", "Interstitial myocarditis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "interstitial myocarditis", "shortest_name_length": 24}
{"curie": "UMLS:C3273260", "names": ["Non-Neoplastic Brain Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Brain Disorder", "shortest_name_length": 29}
{"curie": "MONDO:0005791", "names": ["HERPANGINA", "herpangina", "Herpangina", "Herpanginas", "aphthous pharyngitis", "vesicular pharyngitis", "Herpangina (disorder)", "Vesicular pharyngitis", "PHARYNGITIS, APHTHOUS", "pharyngitis; aphthous", "aphthous; pharyngitis", "PHARYNGITIS, VESICULAR", "vesicular; pharyngitis", "pharyngitis; vesicular", "pharyngitis; coxsackievirus", "coxsackievirus; pharyngitis", "Vesicular pharyngitis (disorder)", "Enteroviral vesicular pharyngitis", "enteroviral vesicular; pharyngitis", "coxsackie group A virus herpangina", "infection; pharynx, Coxsackievirus", "pharyngitis; enteroviral vesicular", "herpangina due to group A coxsackie virus", "herpangina due to group A coxsackie virus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "herpangina", "shortest_name_length": 10}
{"curie": "EFO:1000653", "names": ["sarcopenia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sarcopenia", "shortest_name_length": 10}
{"curie": "MONDO:0011161", "names": ["FA1", "SSFA1", "FERTILIZATION ANTIGEN 1", "fertilization antigen 1", "SPERM-SPECIFIC ANTIGEN 1", "sperm-specific antigen 1", "sperm-specific antigen type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sperm-specific antigen 1", "shortest_name_length": 3}
{"curie": "MONDO:0006705", "names": ["Bacteroidaceae infection", "Bacteroidaceae Infection", "Bacteroidaceae Infections", "Infection, Bacteroidaceae", "infection, Bacteroidaceae", "Infections, Bacteroidaceae", "infections, Bacteroidaceae", "Bacteroidaceae infectious disease", "Bacteroidaceae disease or disorder", "Bacteroidaceae caused disease or disorder", "commensal Bacteroidaceae infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bacteroidaceae infectious disease", "shortest_name_length": 24}
{"curie": "MONDO:0012370", "names": ["DFNB51", "autosomal recessive deafness 51", "DEAFNESS, AUTOSOMAL RECESSIVE 51", "Deafness, autosomal recessive 51", "deafness, autosomal recessive 51", "autosomal recessive nonsyndromic deafness 51", "autosomal recessive nonsyndromic hearing loss 51", "autosomal recessive nonsyndromic deafness type 51"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 51", "shortest_name_length": 6}
{"curie": "MONDO:0007763", "names": ["RCC", "NRC1", "CCRCC", "hypernephroma", "renal cell carcinoma", "adenocarcinoma of kidney", "renal cell carcinoma, somatic", "clear cell renal cell carcinoma", "renal cell carcinoma, clear cell", "nonpapillary renal cell carcinoma", "renal cell carcinoma, nonpapillary", "NONPAPILLARY RENAL CARCINOMA 1 LOCUS", "clear cell renal cell adenocarcinoma", "nonpapillary renal carcinoma 1 locus", "renal carcinoma, chromophobe, somatic", "renal cell carcinoma, clear cell, somatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nonpapillary renal cell carcinoma", "shortest_name_length": 3}
{"curie": "MONDO:0016367", "names": ["DM", "DERMATOMYOSITIS", "dermatomyositis", "Dermatomyositis", "dermatomyositides", "Dermatopolymyositis", "dermatopolymyositis", "DM - Dermatomyositis", "DERMATOMUCOSOMYOSITIS", "dermatomucosomyositis", "Adult dermatomyositis", "adult dermatomyositis", "Amyopathic dermatomyositis", "Wagner-Unverricht syndrome", "WAGNER-UNVERRICHT SYNDROME", "Dermatomyositis (disorder)", "dermatomyositis (diagnosis)", "Polymyositis-Dermatomyositis", "Polymyositis Dermatomyositis", "POLYMYOSITIS DERMATOMYOSITIS", "POLYMYOSITIS/DERMATOMYOSITIS", "Dermatopolymyositis (diagnosis)", "Dermatopolymyositis, unspecified", "polymyositis with skin involvement", "Polymyositis with skin involvement", "polymyositis; with involvement of skin", "Dermatopolymyositis, unspecified, organ involvement unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermatomyositis", "shortest_name_length": 2}
{"curie": "MONDO:0006184", "names": ["DCIS and LCIS of Breast", "DCIS and LCIS of breast", "DCIS and LCIS of the Breast", "DCIS and LCIS of the breast", "Ductal and Lobular Breast Carcinoma in situ", "ductal and lobular breast carcinoma in situ", "Ductal and Lobular Carcinoma in situ of Breast", "ductal and lobular carcinoma in situ of breast", "Intraductal and Lobular Breast Carcinoma in situ", "intraductal and lobular breast carcinoma in situ", "ductal and lobular carcinoma in situ of the breast", "Ductal and Lobular Carcinoma in situ of the Breast", "Intraductal Carcinoma and Lobular Carcinoma in situ", "Intraductal carcinoma and lobular carcinoma in situ", "carcinoma in situ; lobular with intraductal, breast", "intraductal and lobular carcinoma in situ of breast", "breast; carcinoma in situ, lobular with intraductal", "intraductal carcinoma and lobular carcinoma in situ", "Intraductal and Lobular Carcinoma in situ of Breast", "lobular; carcinoma in situ, with intraductal, breast", "Non-Invasive Ductal and Non-Invasive Lobular Carcinoma", "non-invasive ductal and non-invasive lobular carcinoma", "intraductal and lobular carcinoma in situ of the breast", "Intraductal and Lobular Carcinoma in situ of the Breast", "Ductal Breast Carcinoma In Situ and Lobular Carcinoma In Situ", "Breast Ductal Carcinoma In Situ and Lobular Carcinoma In Situ", "ductal breast carcinoma in situ and lobular carcinoma in situ", "Non-Invasive Ductal and Non-Invasive Lobular Breast Carcinoma", "non-invasive ductal and non-invasive lobular breast carcinoma", "Non-Invasive Ductal with Non-Invasive Lobular Breast Carcinoma", "non-invasive ductal with non-invasive lobular breast carcinoma", "intraductal and lobular carcinoma in situ of breast (diagnosis)", "ductal carcinoma in situ with lobular carcinoma in situ of breast", "Ductal Carcinoma in situ with Lobular Carcinoma in situ of Breast", "ductal carcinoma in situ with lobular carcinoma in situ of the breast", "Ductal Carcinoma in situ with Lobular Carcinoma in situ of the Breast", "Non-Infiltrating Ductal and Non-Infiltrating Lobular Breast Carcinoma", "non-infiltrating ductal and non-infiltrating lobular breast carcinoma", "Non-Infiltrating Ductal with Non-Infiltrating Lobular Carcinoma of Breast", "non-infiltrating ductal with non-infiltrating lobular carcinoma of breast", "Non-Invasive Ductal Carcinoma with Non-Invasive Lobular Carcinoma of Breast", "non-invasive ductal carcinoma with non-invasive lobular carcinoma of breast", "Non-Infiltrating Ductal with Non-Infiltrating Lobular Carcinoma of the Breast", "Intraductal carcinoma and lobular carcinoma in situ (morphologic abnormality)", "non-infiltrating ductal with non-infiltrating lobular carcinoma of the breast", "Non-Invasive Ductal Breast Carcinoma with Non-Invasive Lobular Breast Carcinoma", "non-invasive ductal carcinoma with non-invasive lobular carcinoma of the breast", "Non-Invasive Ductal Carcinoma with Non-Invasive Lobular Carcinoma of the Breast", "non-invasive ductal breast carcinoma with non-invasive lobular breast carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ductal breast carcinoma in situ and lobular carcinoma in situ", "shortest_name_length": 23}
{"curie": "UMLS:C0855087", "names": ["Stage I Nodular Sclerosis Hodgkin Lymphoma", "Hodgkin's disease nodular sclerosis stage I", "Nodular Sclerosis Hodgkin's Disease Stage I", "Stage I Nodular Sclerosis Hodgkin's Disease", "Stage I Nodular Sclerosis Hodgkin's Lymphoma", "Nodular Sclerosis Hodgkin's Lymphoma Stage I", "Stage I Nodular Sclerosis Classical Hodgkin Lymphoma", "Hodgkin's disease nodular sclerosis stage I site unspecified", "Ann Arbor Stage I Nodular Sclerosis Classic Hodgkin Lymphoma", "Ann Arbor Stage I Nodular Sclerosis Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's disease nodular sclerosis stage I", "shortest_name_length": 42}
{"curie": "UMLS:C3854347", "names": ["Intentional product misuse", "Intentional product misuses"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intentional product misuse", "shortest_name_length": 26}
{"curie": "UMLS:C3897221", "names": ["Untreated Protoplasmic Astrocytoma", "untreated childhood protoplasmic astrocytoma", "Untreated Childhood Protoplasmic Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Untreated Childhood Protoplasmic Astrocytoma", "shortest_name_length": 34}
{"curie": "MONDO:0044315", "names": ["CRS7", "Crs7, digenic", "CRS7, DIGENIC", "CRANIOSYNOSTOSIS 7", "craniosynostosis 7", "CRANIOSYNOSTOSIS 7, DIGENIC", "craniosynostosis 7, digenic", "craniosynostosis 7, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniosynostosis 7", "shortest_name_length": 4}
{"curie": "MONDO:0021162", "names": ["CAROTENEMIA", "aurantiasis", "carotenemia", "Carotenemia", "carotinosis", "Aurantiasis", "Carotenaemia", "excess; carotene", "hypercarotinemia", "carotene; excess", "Hypercarotenemia", "Hypercarotinemia", "Hypercarotenaemia", "hypercarotenaemia", "Hypercarotinaemia", "acquired carotenemia", "carotenemia (diagnosis)", "Hypercarotinemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carotenemia", "shortest_name_length": 11}
{"curie": "MONDO:0043300", "names": ["AC", "solar cheilitis", "Solar Cheilosis", "Solar Cheilitis", "Actinic Cheilitis", "cheilitis actinic", "Actinic Cheilosis", "actinic cheilitis", "Actinic cheilitis", "actinic cheilosis", "Actinic cheilosis", "actinic; cheilitis", "cheilitis; actinic", "Solar keratosis of lip", "solar keratosis of lip", "Actinic cheilitis (disorder)", "actinic cheilitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "actinic cheilitis", "shortest_name_length": 2}
{"curie": "MONDO:0009368", "names": ["UFS1", "Ochoa syndrome", "urofacial syndrome", "urofacial syndrome 1", "urofacial syndrome type 1", "inverted smile and occult neuropathic bladder", "hydronephrosis with peculiar Facial expression", "facial palsy, partial, with urinary abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urofacial syndrome type 1", "shortest_name_length": 4}
{"curie": "MONDO:0006468", "names": ["ATC", "THAP", "anaplastic cancer thyroid", "Anaplastic thyroid cancer", "anaplastic thyroid cancer", "Anaplastic Thyroid Cancer", "thyroid cancer anaplastic", "Anaplastic Thyroid Cancers", "Thyroid Cancer, Anaplastic", "Cancer, Anaplastic Thyroid", "thyroid cancer, anaplastic", "THYROID, CARCINOMA, SIMPLEX", "Cancers, Anaplastic Thyroid", "Thyroid Cancers, Anaplastic", "THYROID ANAPLASTIC CARCINOMA", "Anaplastic Thyroid Carcinoma", "Thyroid Gland Carcinosarcoma", "Anaplastic thyroid carcinoma", "thyroid gland carcinosarcoma", "anaplastic thyroid carcinoma", "anaplastic carcinoma thyroid", "thyroid carcinoma, anaplastic", "Carcinoma, Anaplastic Thyroid", "Thyroid Carcinoma, Anaplastic", "Anaplastic Thyroid Carcinomas", "undifferentiated thyroid tumor", "Thyroid Carcinomas, Anaplastic", "THYROID, CARCINOMA, ANAPLASTIC", "Undifferentiated Thyroid Tumor", "Carcinomas, Anaplastic Thyroid", "anaplastic carcinoma of thyroid", "undifferentiated thyroid cancer", "cancer thyroid undifferentiated", "carcinosarcoma of thyroid gland", "Anaplastic Carcinoma of Thyroid", "Anaplastic Thyroid Gland Carcinoma", "Thyroid Gland Anaplastic Carcinoma", "undifferentiated thyroid carcinoma", "Undifferentiated Thyroid Carcinoma", "anaplastic thyroid gland carcinoma", "Thyroid Gland Giant Cell Carcinoma", "thyroid gland anaplastic carcinoma", "metaplastic thyroid gland carcinoma", "Thyroid Gland Metaplastic Carcinoma", "anaplastic carcinoma of the thyroid", "Anaplastic Carcinoma of the Thyroid", "Thyroid Gland Sarcomatoid Carcinoma", "sarcomatoid thyroid gland carcinoma", "Thyroid Gland Pleomorphic Carcinoma", "pleomorphic thyroid gland carcinoma", "Sarcomatoid Thyroid Gland Carcinoma", "Metaplastic Thyroid Gland Carcinoma", "Pleomorphic Thyroid Gland Carcinoma", "thyroid cancer, anaplastic carcinoma", "THYROID CANCER, ANAPLASTIC CARCINOMA", "THYROID, CARCINOMA, UNDIFFERENTIATED", "Thyroid Gland Spindle Cell Carcinoma", "undifferentiated carcinoma of thyroid", "anaplastic carcinoma of thyroid gland", "Undifferentiated Carcinoma of Thyroid", "Anaplastic Carcinoma of Thyroid Gland", "spindle cell carcinoma of thyroid gland", "Anaplastic thyroid carcinoma (disorder)", "anaplastic thyroid carcinoma (diagnosis)", "Dedifferentiated thyroid gland carcinoma", "thyroid gland undifferentiated carcinoma", "Undifferentiated Thyroid Gland Carcinoma", "undifferentiated thyroid gland carcinoma", "Dedifferentiated Thyroid Gland Carcinoma", "anaplastic carcinoma of the thyroid gland", "Anaplastic Carcinoma of the Thyroid Gland", "undifferentiated carcinoma of the thyroid", "Undifferentiated Carcinoma of the Thyroid", "thyroid cancer, undifferentiated carcinoma", "Undifferentiated Carcinoma of Thyroid Gland", "spindle cell carcinoma of the thyroid gland", "carcinosarcoma of thyroid gland (diagnosis)", "undifferentiated carcinoma of thyroid gland", "undifferentiated carcinoma of the thyroid gland", "Undifferentiated Carcinoma of the Thyroid Gland", "Undifferentiated (Anaplastic) Thyroid Gland Cancer", "undifferentiated (anaplastic) thyroid gland cancer", "Anaplastic Follicular Cell Derived Thyroid Carcinoma", "Thyroid Gland Undifferentiated (Anaplastic) Carcinoma", "thyroid gland undifferentiated (anaplastic) carcinoma", "undifferentiated (anaplastic) thyroid gland carcinoma", "Undifferentiated (Anaplastic) Thyroid Gland Carcinoma", "spindle cell carcinoma of the thyroid gland (diagnosis)", "Anaplastic Follicular Cell Derived Thyroid Gland Carcinoma", "undifferentiated carcinoma of the thyroid gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid gland undifferentiated (anaplastic) carcinoma", "shortest_name_length": 3}
{"curie": "MONDO:0011020", "names": ["OOCH", "OOCHS", "OOCH syndrome", "Hernandez Fragoso syndrome", "Hernández-Fragoso syndrome", "osteoporosis oculocutaneous hypopigmentation syndrome", "Osteoporosis-oculocutaneous hypopigmentation syndrome", "Osteoporosis oculocutaneous hypopigmentation syndrome", "osteoporosis-oculocutaneous hypopigmentation syndrome", "Osteoporosis and Oculocutaneous Hypopigmentation Syndrome", "Osteoporosis and oculocutaneous hypopigmentation syndrome", "OSTEOPOROSIS AND OCULOCUTANEOUS HYPOPIGMENTATION SYNDROME", "osteoporosis and oculocutaneous hypopigmentation syndrome", "Osteoporosis and oculocutaneous hypopigmentation syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteoporosis-oculocutaneous hypopigmentation syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0015109", "names": ["congenital anomaly of the mitral subvalvular apparatus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital anomaly of the mitral subvalvular apparatus", "shortest_name_length": 54}
{"curie": "MONDO:0005143", "names": ["Pseudomonas aeruginosa PA14 infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pseudomonas aeruginosa PA14 infection", "shortest_name_length": 37}
{"curie": "MONDO:0017804", "names": ["autosomal recessive leukoencephalopathy-ischemic stroke-retinitis pigmentosa syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive leukoencephalopathy-ischemic stroke-retinitis pigmentosa syndrome", "shortest_name_length": 85}
{"curie": "MONDO:0021702", "names": ["alcoholism; Korsakov", "Korsakov; alcoholism", "Alcohol Amnestic Syndrome", "Alcohol amnestic disorder", "alcohol amnestic disorder", "Alcohol Amnestic Disorder", "alcohol amnestic syndrome", "Alcohol amnestic syndrome", "alcohol amnestic syndromes", "Amnestic Disorder, Alcohol", "Alcohol Amnestic Disorders", "amnestic disorder, alcohol", "Alcohol Amnestic Syndromes", "syndrome, alcohol amnestic", "alcohol amnestic disorders", "amnestic syndrome, alcohol", "alcohol; amnestic syndrome", "amnestic disorders, alcohol", "syndromes, alcohol amnestic", "amnestic syndromes, alcohol", "Alcoholic amnestic syndrome", "syndrome; amnestic, alcohol", "alcoholic korsakoff syndrome", "alcoholic Korsakoff syndrome", "psychosis; Korsakov, alcohol", "Korsakov alcoholic psychosis", "alcoholic Korsakoff syndromes", "syndrome, alcoholic Korsakoff", "Korsakov syndrome - alcoholic", "Korsakoff syndrome, alcoholic", "syndromes, alcoholic Korsakoff", "alcoholic Korsakov's psychosis", "Korsakoffs alcoholic psychosis", "Korsakoff syndromes, alcoholic", "Korsakoffs psychosis;alcoholic", "psychosis; alcoholic, Korsakov", "alcoholic Korsakoff's syndrome", "Korsakov's psychosis, alcoholic", "Korsakoff's psychosis alcoholic", "Amnesic syndrome due to alcohol", "alcohol induced amnestic syndrome", "Alcohol Induced Amnestic Syndrome", "alcohol-induced amnestic syndrome", "Alcohol-Induced Amnestic Syndrome", "alcohol-induced Korsakoff syndrome", "Amnestic Syndrome, Alcohol-Induced", "alcohol-induced amnestic psychosis", "Alcohol-Induced Amnestic Syndromes", "alcohol induced amnestic psychosis", "syndrome, alcohol-induced amnestic", "alcohol-induced Dysmnesic syndrome", "Alcohol Induced Amnestic Psychosis", "alcohol induced Korsakoff syndrome", "amnestic syndrome, alcohol-induced", "alcohol-induced amnestic psychoses", "alcohol-induced amnestic syndromes", "Alcohol-Induced Amnestic Psychoses", "alcohol induced Dysmnesic syndrome", "Alcohol-Induced Dysmnesic Syndrome", "psychosis; alcoholic, polyneuritic", "Alcohol-Induced Amnestic Psychosis", "Alcohol Induced Dysmnesic Syndrome", "alcohol-induced Dysmnesic psychosis", "Alcohol-Induced Dysmnesic Syndromes", "Korsakoff syndrome, alcohol-induced", "Amnestic Psychoses, Alcohol-Induced", "Alcohol-Induced Dysmnesic Psychoses", "amnestic syndromes, alcohol-induced", "Alcohol-Induced Dysmnesic Psychosis", "syndromes, alcohol-induced amnestic", "Alcohol Induced Dysmnesic Psychosis", "syndrome, alcohol-induced Korsakoff", "Dysmnesic Syndrome, Alcohol-Induced", "Amnestic Psychosis, Alcohol Induced", "Amnestic Psychosis, Alcohol-Induced", "alcohol induced Dysmnesic psychosis", "alcohol-induced Dysmnesic syndromes", "Amnestic Syndromes, Alcohol-Induced", "syndrome, alcohol-induced Dysmnesic", "psychosis, alcohol-induced amnestic", "psychoses, alcohol-induced amnestic", "alcohol-induced Dysmnesic psychoses", "amnestic psychosis, alcohol-induced", "Psychoses, Alcohol-Induced Amnestic", "alcohol-induced Korsakoff syndromes", "Psychosis, Alcohol-Induced Amnestic", "amnestic; syndrome, alcohol-induced", "amnestic psychoses, alcohol-induced", "Dysmnesic syndrome, alcohol-induced", "syndrome; amnestic, alcohol-induced", "amnestic psychosis, alcohol induced", "psychoses, alcohol-induced Dysmnesic", "Dysmnesic psychoses, alcohol-induced", "Alcohol amnestic disorder (disorder)", "Dysmnesic syndromes, alcohol-induced", "Korsakoff syndromes, alcohol-induced", "Dysmnesic psychosis, alcohol-induced", "psychosis, alcohol-induced Dysmnesic", "Psychosis, Alcohol-Induced Dysmnesic", "Dysmnesic Psychoses, Alcohol-Induced", "Psychoses, Alcohol-Induced Dysmnesic", "Dysmnesic Syndromes, Alcohol-Induced", "Dysmnesic Psychosis, Alcohol-Induced", "syndromes, alcohol-induced Korsakoff", "syndromes, alcohol-induced Dysmnesic", "Alcohol-induced persisting amnestic disorder", "alcohol induced persisting amnestic disorder", "Alcohol-Induced Persisting Amnestic Disorder", "alcohol-induced persisting amnestic disorder", "Alcohol Induced Persisting Amnestic Disorder", "alcohol-induced persisting amnestic disorder (diagnosis)", "Mental and behavioral disorders due to use of alcohol, amnesic syndrome", "Mental and behavioural disorders due to use of alcohol, amnesic syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alcohol amnestic disorder", "shortest_name_length": 20}
{"curie": "UMLS:C4683593", "names": ["Lugano Classification Stage IV Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage IV Hodgkin Lymphoma AJCC v8", "shortest_name_length": 55}
{"curie": "UMLS:C3897530", "names": ["Stage IIIB Esophageal Cancer", "Stage IIIB Esophageal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Esophageal Cancer AJCC v7", "shortest_name_length": 28}
{"curie": "UMLS:C0341177", "names": ["erosion stomach", "gastric erosion", "stomach erosion", "erosions stomach", "gastric erosions", "Gastric erosions", "Multiple gastric erosions", "Multiple gastric erosions (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric erosions", "shortest_name_length": 15}
{"curie": "MONDO:0030029", "names": ["SDJLABA", "skeletal dysplasia, mild, with joint laxity and advanced bone age", "SKELETAL DYSPLASIA, MILD, WITH JOINT LAXITY AND ADVANCED BONE AGE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skeletal dysplasia, mild, with joint laxity and advanced bone age", "shortest_name_length": 7}
{"curie": "MONDO:0003705", "names": ["adult brainstem mixed glioma", "Adult Brainstem Mixed Glioma", "mixed glioma, adult brainstem", "adult brain stem mixed glioma", "Adult Brain Stem Mixed Glioma", "mixed glioma, adult brain stem"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult brainstem mixed glioma", "shortest_name_length": 28}
{"curie": "UMLS:C4055248", "names": ["Childhood AML with NUP98 Rearrangement", "Childhood Acute Myeloid Leukemia with NUP98 Rearrangement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Acute Myeloid Leukemia with NUP98 Rearrangement", "shortest_name_length": 38}
{"curie": "MONDO:0001079", "names": ["Pancreatic steatorrhea", "pancreatic steatorrhea", "pancreatic steatorrhoea", "pancreatic; steatorrhea", "Pancreatic steatorrhoea", "steatorrhea; pancreatic", "Pancreatic steatorrhea syndrome", "Pancreatic steatorrhea (disorder)", "pancreatic steatorrhea (diagnosis)", "pancreas; decreased tolerance (steatorrhea)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic steatorrhea", "shortest_name_length": 22}
{"curie": "UMLS:C0751851", "names": ["Arsenic encephalopathy", "Arsenic Encephalopathy", "Encephalopathy, Arsenic", "Arsenic Encephalopathies", "Encephalopathies, Arsenic", "Encephalopathy caused by arsenic", "Disorder of brain caused by arsenic", "Disorder of brain caused by arsenic (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arsenic Encephalopathy", "shortest_name_length": 22}
{"curie": "MONDO:0005672", "names": ["Gilchrist", "blastomycosis", "Blastomycoses", "blastomycoses", "BLASTOMYCOSIS", "Blastomycosis", "chicago disease", "Chicago disease", "Chicago; disease", "Gilchrist Disease", "Gilchrists Disease", "Blastomycosis, NOS", "gilchrist's disease", "Gilchrist's disease", "Gilchrist's Disease", "Blastomyces infections", "Blastomyces; infection", "infection; Blastomyces", "Blastomycotic infection", "blastomycotic infection", "Infection by Blastomyces", "Blastomycosis (disorder)", "blastomycosis (diagnosis)", "Blastomycosis, unspecified", "north American blastomycosis", "North American blastomycosis", "Blastomycotic infection, NOS", "North American Blastomycosis", "blastomycosis; North American", "Blastomycosis, North American", "Infection by Blastomyces, NOS", "BLASTOMYCOSIS, NORTH AMERICAN", "North American; blastomycotic", "disease (or disorder); Chicago", "Blastomyces dermatitidis infection", "Blastomyces Dermatitidis Infection", "blastomycotic infection (diagnosis)", "Infection by Blastomyces dermatitidis", "infection by Blastomyces dermatitidis", "North American blastomycosis (diagnosis)", "Blastomyces dermatitidis infectious disease", "Blastomyces dermatitidis disease or disorder", "Infection caused by Blastomyces dermatitidis", "Blastomyces dermatitidis caused disease or disorder", "infection; Blastomyces, blastomycotic, dermatitidis", "infection; Blastomyces, blastomycotic, North American", "Infection caused by Blastomyces dermatitidis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blastomycosis", "shortest_name_length": 9}
{"curie": "UMLS:C3898626", "names": ["Lamellar laceration of the globe", "Lamellar Laceration of the Globe"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lamellar laceration of the globe", "shortest_name_length": 32}
{"curie": "MONDO:0002675", "names": ["MPNST", "MPNST, NOS", "Neurosarcoma", "neurosarcoma", "neurosarcomas", "Melanotic MPNST", "neurofibrosarcoma", "NEUROFIBROSARCOMA", "Neurofibrosarcoma", "neurofibrosarcomas", "Neurogenic sarcoma", "neurosarcoma [obs]", "Neurofibrosarcomas", "Neurogenic Sarcoma", "neurogenic sarcoma", "Sarcoma, Neurogenic", "Neurogenic Sarcomas", "neurogenic sarcomas", "Sarcomas, Neurogenic", "Malignant Schwannoma", "Malignant schwannoma", "SCHWANNOMA, MALIGNANT", "Neurofibrosarcoma NOS", "Neurilemoma, malignant", "Malignant Neurilemmoma", "Neurofibrosarcoma, Malignant", "Melanotic psammomatous MPNST", "Melanocytic Psammomatous MPNST", "Malig. periph. nerve sheath tum.", "MPNST with mesenchymal differentiation", "Malignant Peripheral Nerve Sheath Tumor", "malignant peripheral nerve sheath tumor", "Malignant peripheral nerve sheath tumor", "Malignant Peripheral Nerve Sheath Tumour", "Malignant peripheral nerve sheath tumour", "Malignant Peripheral Nerve Sheath Neoplasm", "Malignant Melanotic Psammomatous Peripheral Nerve Sheath Tumor", "Melanotic Psammomatous Malignant Peripheral Nerve Sheath Tumor", "Melanocytic Psammomatous Malignant Peripheral Nerve Sheath Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurofibrosarcoma", "shortest_name_length": 5}
{"curie": "UMLS:C0853708", "names": ["sle arthritis", "SLE arthritis", "arthritis sle"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SLE arthritis", "shortest_name_length": 13}
{"curie": "UMLS:C2931150", "names": ["Unilateral Coronal Synostoses", "Unilateral coronal synostosis", "Unilateral Coronal Synostosis", "Synostosis, Unilateral Coronal", "Synostoses, Unilateral Coronal", "Coronal synostosis, unilateral", "Coronal Synostoses, Unilateral", "Coronal Synostosis, Unilateral", "Synostotic Anterior Plagiocephaly", "Anterior Plagiocephaly, Synostotic", "Plagiocephaly, Synostotic Anterior"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Synostotic Anterior Plagiocephaly", "shortest_name_length": 29}
{"curie": "UMLS:C0403643", "names": ["Bladder muscle dysfunction - overactive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder muscle dysfunction - overactive", "shortest_name_length": 39}
{"curie": "MONDO:0012673", "names": ["CRCS2", "colorectal cancer, susceptibility to, 2", "COLORECTAL CANCER, SUSCEPTIBILITY TO, 2", "colorectal cancer, susceptibility to, on chromosome 8Q24", "COLORECTAL CANCER, SUSCEPTIBILITY TO, ON CHROMOSOME 8q24"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorectal cancer, susceptibility to, 2", "shortest_name_length": 5}
{"curie": "MONDO:0013626", "names": ["GPP", "PSORP", "DITRA", "PSORS14", "acropustulosis", "IL36RN psoriasis", "Dermatitis repens", "repens; dermatitis", "dermatitis; repens", "Deficiency of IL-36Ra", "pustular psoriasis 14", "deficiency of IL-36Ra", "PSORIASIS 14, PUSTULAR", "psoriasis 14, pustular", "PALMOPLANTAR PUSTULOSIS", "Acrodermatitis continua", "ACRODERMATITIS CONTINUA", "Acrodermatitis perstans", "palmoplantar pustulosis", "acrodermatitis continua", "perstans; acrodermatitis", "acrodermatitis; perstans", "acrodermatitis; continua", "continua; acrodermatitis", "generalized pustular psoriasis", "GENERALIZED PUSTULAR PSORIASIS", "Deficiency of IL-36R antagonist", "deficiency of IL-36R antagonist", "Acrodermatitis perstans continua", "acrodermatitis continua hallopeau", "acrodermatitis continua (diagnosis)", "ACRODERMATITIS CONTINUA OF HALLOPEAU", "Acrodermatitis continua of Hallopeau", "acrodermatitis continua of Hallopeau", "psoriasis caused by mutation in IL36RN", "Familial Generalized Pustular Psoriasis", "familial generalized pustular psoriasis", "Interleukin 36 receptor antagonist deficiency", "INTERLEUKIN 36 RECEPTOR ANTAGONIST DEFICIENCY", "Acrodermatitis continua of Hallopeau (disorder)", "Deficiency of interleukin 36 receptor antagonist", "acrodermatitis continua suppurativa of Hallopeau", "Recalcitrant pustular eruption of palms and soles", "Recalcitrant Pustular Eruptions of Palms and Soles", "deficiency of the interleukin-36 receptor antagonist", "Deficiency of the Interleukin-36 Receptor Antagonist", "Deficiency of the interleukin-36 receptor antagonist", "DITRA - deficiency of interleukin 36 receptor antagonist", "Deficiency of IL-36Ra (interleukin 36 receptor antagonist)", "Deficiency of interleukin 36 receptor antagonist (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "psoriasis 14, pustular", "shortest_name_length": 3}
{"curie": "UMLS:C2217039", "names": ["Stage IIIC Colon Cancer", "Stage IIIC Colon Cancer AJCC v7", "malignant large intestine neoplasm stage IIIc", "malignant large intestine neoplasm stage IIIc (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Colon Cancer AJCC v7", "shortest_name_length": 23}
{"curie": "UMLS:C0745138", "names": ["Hypertensive urgency", "HYPERTENSIVE URGENCY", "hypertensive urgency", "hypertensive urgencies", "Hypertensive urgency (disorder)", "hypertensive urgency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypertensive urgency", "shortest_name_length": 20}
{"curie": "MONDO:0100308", "names": ["ataxia", "ataxic disorder", "atactic disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atactic disorder", "shortest_name_length": 6}
{"curie": "MONDO:0042966", "names": ["Mitral anomaly", "mitral; anomaly", "anomaly; mitral", "inherited mitral valve disease", "hereditary mitral valve disease", "congenital anomaly of mitral valve", "Congenital anomaly of mitral valve", "congenital mitral valve abnormality", "Congenital mitral valve abnormality", "mitral(valve); deformity, congenital", "deformity; mitral(valve), congenital", "Congenital anomaly of mitral valve, NOS", "Congenital malformation of mitral valve", "congenital malformation of mitral valve", "MV - Congenital mitral valve abnormality", "mitral valve disorder congenital malformation", "Congenital anomaly of mitral valve (disorder)", "congenital malformation of mitral valve (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited mitral valve disease", "shortest_name_length": 14}
{"curie": "MONDO:0004345", "names": ["Pediatric MPNST", "childhood MPNST", "Childhood MPNST", "pediatric MPNST", "Childhood Neurofibrosarcoma", "childhood neurofibrosarcoma", "pediatric neurofibrosarcoma", "neurofibrosarcoma, childhood", "Childhood Neurogenic Sarcoma", "neurofibrosarcoma, pediatric", "childhood neurogenic sarcoma", "neurogenic sarcoma, childhood", "sarcoma, neurogenic, childhood", "pediatric malignant schwannoma", "Childhood Malignant Schwannoma", "Pediatric Malignant Schwannoma", "childhood malignant schwannoma", "malignant neurolemma, childhood", "sarcoma, neurofibro-, childhood", "malignant schwannoma, childhood", "Childhood Malignant Neurilemmoma", "childhood malignant neurilemmoma", "Pediatric Malignant Neurilemmoma", "schwannoma, malignant, childhood", "pediatric malignant neurilemmoma", "neurolemma, malignant, childhood", "Malignant Peripheral Nerve Sheath Tumor", "malignant peripheral nerve sheath tumor", "Pediatric Malignant Peripheral Nerve Sheath Tumor", "Childhood Malignant Peripheral Nerve Sheath Tumor", "childhood malignant peripheral nerve sheath tumor", "pediatric malignant peripheral nerve sheath tumor", "Pediatric Malignant Tumor of Peripheral Nerve Sheath", "childhood malignant tumor of peripheral nerve sheath", "pediatric malignant tumor of peripheral nerve sheath", "Childhood Malignant Tumor of Peripheral Nerve Sheath", "pediatric malignant peripheral nerve sheath neoplasm", "Pediatric Malignant Peripheral Nerve Sheath Neoplasm", "Childhood Malignant Peripheral Nerve Sheath Neoplasm", "childhood malignant peripheral nerve sheath neoplasm", "Pediatric Malignant Neoplasm of Peripheral Nerve Sheath", "childhood malignant neoplasm of peripheral nerve sheath", "Childhood Malignant Neoplasm of Peripheral Nerve Sheath", "pediatric malignant neoplasm of peripheral nerve sheath", "pediatric malignant tumor of the peripheral nerve sheath", "childhood malignant tumor of the peripheral nerve sheath", "Childhood Malignant Tumor of the Peripheral Nerve Sheath", "Pediatric Malignant Tumor of the Peripheral Nerve Sheath", "Childhood Malignant Neoplasm of the Peripheral Nerve Sheath", "childhood malignant neoplasm of the peripheral nerve sheath", "Pediatric Malignant Neoplasm of the Peripheral Nerve Sheath", "pediatric malignant neoplasm of the peripheral nerve sheath"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood malignant schwannoma", "shortest_name_length": 15}
{"curie": "UMLS:C2945586", "names": ["Unstable bladder", "Irritable;bladder", "Irritable bladder", "irritable bladder", "BLADDER IRRITATION", "Bladder irritation", "bladder; irritable", "Bladder instability", "Instability;bladder", "irritation; bladder", "BLADDER INSTABILITY", "bladder; irritation", "bladder irritability", "Bladder irritability", "irritability; bladder", "instability of the bladder", "Bladder irritability (finding)", "bladder irritability (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder irritability", "shortest_name_length": 16}
{"curie": "UMLS:C4683019", "names": ["Stage IIIB Eyelid Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Eyelid Carcinoma AJCC v8", "shortest_name_length": 35}
{"curie": "MONDO:0007206", "names": ["bone pain, periodic", "BONE PAIN, PERIODIC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bone pain, periodic", "shortest_name_length": 19}
{"curie": "UMLS:C0948227", "names": ["Renal Pelvis Fistula", "Renal pelvis fistula"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal pelvis fistula", "shortest_name_length": 20}
{"curie": "MONDO:0022825", "names": ["CCE", "congenital cystic eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital cystic eye", "shortest_name_length": 3}
{"curie": "UMLS:C1516074", "names": ["Astler-Coller C3 Colorectal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Astler-Coller C3 Colorectal Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0001108", "names": ["broad ligament of uterus cancer", "malignant broad ligament neoplasm", "broad ligament malignant neoplasm", "Malignant Broad Ligament Neoplasm", "malignant tumor of broad ligament", "Cancer of broad ligament of uterus", "cancer of broad ligament of uterus", "Malignant neoplasm of broad ligament", "malignant neoplasm of broad ligament", "malignant broad ligament of uterus neoplasm", "Malignant neoplasm of broad ligament of uterus", "malignant neoplasm of broad ligament of uterus", "malignant neoplasm of broad ligament (diagnosis)", "Malignant neoplasm of broad ligament of uterus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "broad ligament malignant neoplasm", "shortest_name_length": 31}
{"curie": "UMLS:C5421284", "names": ["Digestive System Leiomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Digestive System Leiomyosarcoma", "shortest_name_length": 31}
{"curie": "MONDO:0016140", "names": ["Sarcoglycanopathy", "sarcoglycanopathy", "Sarcoglycanopathies", "Sarcoglycanopathy, NOS", "Qualitative or quantitative defects of sarcoglycan", "qualitative or quantitative defects of sarcoglycan"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sarcoglycanopathy", "shortest_name_length": 17}
{"curie": "MONDO:0024555", "names": ["VL", "Lvm", "MLC1", "Van Der Knaap disease", "leukoencephalopathy with swelling and cysts", "megalencephalic leukoencephalopathy with subcortical cysts", "megalencephalic leukoencephalopathy with subcortical cysts 1", "Vacuolating megalencephalic leukoencephalopathy with subcortical cysts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "megalencephalic leukoencephalopathy with subcortical cysts 1", "shortest_name_length": 2}
{"curie": "UMLS:C0339467", "names": ["proliferative retinopathy", "Retinopathy proliferative", "Proliferative retinopathy", "Proliferative Retinopathy", "RETINOPATHY PROLIFERATIVE", "proliferative; retinopathy", "retinopathy; proliferative", "Proliferative retinopathy (disorder)", "proliferative retinopathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Proliferative retinopathy", "shortest_name_length": 25}
{"curie": "MONDO:0003767", "names": ["Mitral valve disease", "mitral RH valve dis.", "disease mitral valve", "mitral valve disease", "Mitral RH valve dis.", "MITRAL VALVE DISEASE", "mitral valve diseases", "Mitral valve abnormal", "Mitral valve disorder", "mitral valve disorder", "Abnormal mitral valve", "Mitral Valve Disorder", "mitral valve; disorder", "Mitral valve disorders", "mitral valve disorders", "mitral valvular disease", "disease of mitral valve", "Mitral valve disease NOS", "disorder of mitral valve", "Diseases of mitral valve", "Valvular disease (mitral)", "Mitral valve disorder, NOS", "MVD - Mitral valve disease", "Rheumatic mitral incompetence", "MITRAL REGURGITATION RHEUMATIC", "chronic rheumatic mitral valve", "Rheumatic mitral valve changes", "rheumatic mitral regurgitation", "Rheumatic mitral insufficiency", "rheumatic mitral insufficiency", "rheumatic mitral valve changes", "Rheumatic mitral regurgitation", "Mitral incompetence - rheumatic", "insufficiency; mitral, rheumatic", "mitral valve disease or disorder", "Mitral valve disorder (disorder)", "mitral valve disorder (diagnosis)", "rheumatic disease of mitral valve", "disease or disorder of mitral valve", "Rheumatic mitral valve incompetence", "Chronic rheumatic mitral valvulitis", "rheumatic mitral valve incompetence", "Rheumatic mitral valve insufficiency", "rheumatic mitral valve regurgitation", "Rheumatic mitral valve regurgitation", "chronic rheumatic mitral valve disorder", "mitral valve disorder rheumatic, chronic", "Rheumatic mitral regurgitation (disorder)", "rheumatic mitral regurgitation (diagnosis)", "Rheumatic heart disease with mitral valvulitis", "chronic rheumatic mitral valve disorder (diagnosis)", "Chronic rheumatic heart disease with mitral valvulitis", "Chronic mitral valvulitis due to rheumatic heart disease", "Chronic mitral valvulitis due to rheumatic heart disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitral valve disorder", "shortest_name_length": 20}
{"curie": "MONDO:0024610", "names": ["skin parasite", "parasite skin", "parasites skin", "skin parasites", "parasitism; skin", "skin infestation", "skin; parasitism", "infestations skin", "parasitic dermatitis", "parasitic skin disease", "Parasitic Skin Disease", "parasitic diseases skin", "Skin Disease, Parasitic", "parasitic skin disorder", "Disease, Parasitic Skin", "parasitic skin diseases", "disease, parasitic skin", "skin disease, parasitic", "Parasitic Skin Diseases", "Skin Diseases, Parasitic", "parasitic; disease, skin", "Diseases, Parasitic Skin", "diseases, parasitic skin", "parasitic skin disorders", "parasitic skin infestation", "Parasitic infection of skin", "parasitic; infestation, skin", "parasitic dermatological conditions", "parasitic skin disorders (diagnosis)", "disease (or disorder); parasitic, skin", "Parasitic infection of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parasitic skin disorder", "shortest_name_length": 13}
{"curie": "UMLS:C2828189", "names": ["Stage IIIA Gestational Trophoblastic Tumor", "Stage IIIA Gestational Trophoblastic Tumor AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Gestational Trophoblastic Tumor AJCC v7", "shortest_name_length": 42}
{"curie": "MONDO:0006502", "names": ["ALI", "ARDS", "Adult RDS", "Stiff lung", "shock lung", "acute lung injury", "non-cardiogenic pulmonary edema", "Adult respiratory distress syndrome", "acute respiratory distress syndrome", "Acute Respiratory Distress Syndrome", "Adult Respiratory Distress Syndrome", "increased-permeability pulmonary edema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute respiratory distress syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C0748404", "names": ["Metastatic Rhabdomyosarcoma", "RHABDOMYOSARCOMA METASTATIC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Rhabdomyosarcoma", "shortest_name_length": 27}
{"curie": "UMLS:C0279922", "names": ["Childhood MCHD", "Pediatric MCHD", "MCHD, childhood", "MC HD, childhood", "pediatric HD, mixed cellularity", "mixed cellularity HD, childhood", "childhood HD, mixed cellularity", "HD, mixed cellularity, childhood", "Mixed Cellularity Classical Hodgkin Lymphoma", "Childhood Mixed Cellularity Hodgkin Lymphoma", "childhood mixed cellularity Hodgkin lymphoma", "Childhood Mixed Cellularity Hodgkin's Disease", "Pediatric Mixed Cellularity Hodgkin's Disease", "mixed cellularity childhood Hodgkin's disease", "pediatric mixed cellularity Hodgkin's disease", "childhood mixed cellularity Hodgkin's disease", "childhood Hodgkin's disease, mixed cellularity", "Pediatric Mixed Cellularity Hodgkin's Lymphoma", "pediatric Hodgkin's disease, mixed cellularity", "mixed cellularity Hodgkin's disease, childhood", "Childhood Mixed Cellularity Hodgkin's Lymphoma", "Hodgkin's disease, mixed cellularity, childhood", "lymphoma, mixed cellularity childhood Hodgkin's", "Childhood Mixed Cellularity Classic Hodgkin Lymphoma", "Childhood Mixed Cellularity Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Mixed Cellularity Classic Hodgkin Lymphoma", "shortest_name_length": 14}
{"curie": "UMLS:C0277825", "names": ["bone sequestrum", "Bone sequestrum", "bone; sequestrum", "Sequestrum, bone", "sequestrum; bone", "Sequestrum of bone", "Bone sequestration", "Bone sequestrum (disorder)", "bone sequestrum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone sequestrum", "shortest_name_length": 15}
{"curie": "UMLS:C0858751", "names": ["Lip blister", "Blister lip", "lip blister", "blister lip", "blister lips", "blisters lip", "blisters lips", "blister of lip", "Blister of lip", "blistering lip", "blistered lips", "Blister of lip (disorder)", "blister of lip (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Blister of lip", "shortest_name_length": 11}
{"curie": "MONDO:0020325", "names": ["ALCL", "sACL", "Ki-1+ ALCL", "Ki-1 Lymphoma", "ki-1 lymphoma", "Ki 1 Lymphoma", "ki 1 lymphoma", "Ki-1 lymphoma", "Ki-1 Lymphomas", "Lymphoma, Ki-1", "Lymphomas, Ki-1", "(Ki-1+) lymphoma", "primary systemic ALCL", "Primary systemic ALCL", "Lymphoma, Large-Cell, Ki-1", "Large cell (Ki-1+) lymphoma", "Anaplastic large cell lymphoma", "anaplastic large cell lymphoma", "Anaplastic large-cell lymphoma", "large cell anaplastic lymphoma", "Anaplastic Large Cell Lymphoma", "Anaplastic Large-Cell Lymphoma", "Large cell anaplastic lymphoma", "Lymphoma, Anaplastic Large-Cell", "Anaplastic Large-Cell Lymphomas", "lymphoma, anaplastic large cell", "Large-Cell Lymphoma, Anaplastic", "Large-Cell Lymphomas, Anaplastic", "Lymphomas, Anaplastic Large-Cell", "Lymphoma, Large-Cell, Anaplastic", "Large cell (Ki-1 positive) lymphoma", "NHL, anaplastic large cell lymphoma", "Anaplastic large cell lymphoma, NOS", "Ki-1+ Anaplastic Large Cell Lymphoma", "Ki-1+ anaplastic large cell lymphoma", "CD30+ Anaplastic Large Cell Lymphoma", "CD30+ Anaplastic Large-Cell Lymphoma", "Anaplastic large cell lymphoma, CD30+", "Systemic Anaplastic Large Cell Lymphoma", "Systemic Anaplastic Large-Cell Lymphoma", "anaplastic large cell lymphoma (diagnosis)", "Anaplastic large cell lymphoma (ALCL) CD30+", "Anaplastic large cell lymphoma CD30 positive", "CD30 Positive Anaplastic Large Cell Lymphoma", "CD30 Positive anaplastic large cell lymphoma", "Ki-1 positive anaplastic large cell lymphoma", "CD30-Positive Anaplastic Large-Cell Lymphoma", "CD30 positive anaplastic large cell lymphoma", "Anaplastic large cell lymphoma, CD30-positive", "lymphoma anaplastic large cell T cell and null cell type", "Large cell anaplastic lymphoma T cell and Null cell type", "anaplastic large cell lymphoma T cell and null cell type", "Anaplastic large cell lymphoma, T cell and Null cell type", "Large cell anaplastic lymphoma T cell and Null cell type (disorder)", "anaplastic large cell lymphoma T cell and null cell type (diagnosis)", "Anaplastic large cell lymphoma, T cell and Null cell type (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anaplastic large cell lymphoma", "shortest_name_length": 4}
{"curie": "MONDO:0007353", "names": ["SORSBY SYNDROME", "Sorsby syndrome", "apical dystrophy", "APICAL DYSTROPHY", "Coloboma of macula type B brachydactyly", "COLOBOMA OF MACULA WITH TYPE B BRACHYDACTYLY", "Coloboma Of Macula With Type B Brachydactyly", "coloboma of macula with type B brachydactyly", "Coloboma of macula-brachydactyly type B syndrome", "coloboma of macula-brachydactyly type B syndrome", "Coloboma of macula with brachydactyly type B syndrome", "Coloboma of macula with brachydactyly type B syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coloboma of macula-brachydactyly type B syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0032699", "names": ["EIG15", "idiopathic generalized epilepsy 15", "Susceptibility to Idiopathic Generalized Epilepsy-15", "epilepsy, idiopathic generalized, susceptibility to, 15", "EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 15"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, idiopathic generalized, susceptibility to, 15", "shortest_name_length": 5}
{"curie": "MONDO:0001823", "names": ["SSS", "Sick sinus syndrome", "SICK SINUS SYNDROME", "Sick Sinus Syndrome", "sick sinus syndrome", "sick syndrome sinus", "SYNDROME SICK SINUS", "sinus sick syndrome", "Syndrome sick sinus", "Syndrome, sick sinus", "Syndrome, Sick Sinus", "sinus node infection", "sick sinus; syndrome", "syndrome; sick sinus", "Sinoatrial node disease", "Sick Sinus Node Syndrome", "Sick sinus syndrome (disorder)", "sick sinus syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sick sinus syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0700122", "names": ["PBRM1-related BAFopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PBRM1-related BAFopathy", "shortest_name_length": 23}
{"curie": "MONDO:0009002", "names": ["COLOBOMA, OCULAR, AUTOSOMAL RECESSIVE", "coloboma, ocular, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coloboma, ocular, autosomal recessive", "shortest_name_length": 37}
{"curie": "MONDO:0100304", "names": ["disorder of bile acid aminotransferase"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of bile acid aminotransferase", "shortest_name_length": 38}
{"curie": "MONDO:0003606", "names": ["adrenal medulla tumor", "adrenal medulla cancer", "adrenal medulla neoplasm", "cancer of adrenal medulla", "malignant adrenal medulla tumor", "Malignant Adrenal Medulla Tumor", "Malignant tumor of adrenal medulla", "malignant tumor of adrenal medulla", "Malignant Tumor of Adrenal Medulla", "malignant adrenal medulla neoplasm", "Malignant Adrenal Medulla Neoplasm", "Malignant tumour of adrenal medulla", "Malignant Neoplasm of Adrenal Medulla", "malignant neoplasm of adrenal medulla", "Malignant neoplasm of adrenal medulla", "Malignant Tumor of the Adrenal Medulla", "malignant tumor of the adrenal medulla", "malignant tumor of the Adrenal Medulla", "Malignant Neoplasm of the Adrenal Medulla", "malignant neoplasm of the adrenal medulla", "Malignant neoplasm of medulla of adrenal gland", "Malignant neoplasm of adrenal medulla (disorder)", "malignant neoplasm of adrenal medulla (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adrenal medulla cancer", "shortest_name_length": 21}
{"curie": "MONDO:0004853", "names": ["gonococcal endophthalmia", "Gonococcal endophthalmia", "gonococcal endophthalmitis", "Gonococcal endophthalmia (disorder)", "gonococcal endophthalmitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gonococcal endophthalmia", "shortest_name_length": 24}
{"curie": "MONDO:0012627", "names": ["ECA4", "EJM5", "EIG13", "idiopathic generalized epilepsy 13", "GABRA1 juvenile myoclonic epilepsy", "epilepsy, childhood absence, susceptibility to, 4", "EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 4", "Epilepsy, Childhood Absence, Susceptibility To, 4", "epilepsy, juvenile myoclonic, susceptibility to, 5", "EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 5", "susceptibility to idiopathic generalized epilepsy 13", "EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 13", "epilepsy, idiopathic generalized, susceptibility to, 13", "juvenile myoclonic epilepsy caused by mutation in GABRA1", "epilepsy, idiopathic generalized, susceptibility to, type 13", "EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 5 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, idiopathic generalized, susceptibility to, 13", "shortest_name_length": 4}
{"curie": "UMLS:C4727431", "names": ["Refractory Malignant Brain Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Malignant Brain Neoplasm", "shortest_name_length": 35}
{"curie": "UMLS:C0235064", "names": ["RESPIRATORY DEPRESSION NEONATAL", "Respiratory depression neonatal", "Neonatal respiratory depression", "Neonatal respiratory depression (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neonatal respiratory depression", "shortest_name_length": 31}
{"curie": "MONDO:0006348", "names": ["Pancreatic Small Cell NEC", "pancreatic small cell NEC", "pancreatic small cell NEC G3", "Pancreatic Small Cell NEC G3", "Pancreatic Small Cell Carcinoma", "endocrine pancreas small cell carcinoma", "small cell carcinoma of endocrine pancreas", "pancreatic small cell neuroendocrine carcinoma", "Pancreatic Small Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic small cell neuroendocrine carcinoma", "shortest_name_length": 25}
{"curie": "UMLS:C0853089", "names": ["Deliberate self-injury", "Intentional self-injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intentional self-injury", "shortest_name_length": 22}
{"curie": "UMLS:C4331824", "names": ["ADNDI", "Autosomal Dominant Neurohypophyseal Diabetes Insipidus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Autosomal Dominant Neurohypophyseal Diabetes Insipidus", "shortest_name_length": 5}
{"curie": "MONDO:0013264", "names": ["ALS12", "ALS12 (diagnosis)", "amyotrophic lateral sclerosis 12", "AMYOTROPHIC LATERAL SCLEROSIS 12", "OPTN amyotrophic lateral sclerosis", "amyotrophic lateral sclerosis ALS12", "amyotrophic lateral sclerosis type 12", "amyotrophic lateral sclerosis caused by mutation in OPTN", "AMYOTROPHIC LATERAL SCLEROSIS 12 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA", "amyotrophic lateral sclerosis 12 with or without frontotemporal dementia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyotrophic lateral sclerosis type 12", "shortest_name_length": 5}
{"curie": "MONDO:0018079", "names": ["TEN", "Tet", "thymoma, adult", "Thymoma, adult", "Thymus epithelial tumor", "Thymic epithelial tumor", "thymic epithelial tumor", "Thymic Epithelial Tumor", "Thymus Epithelial Tumor", "thymus epithelial neoplasm", "Thymic Epithelium Neoplasm", "Thymic epithelial neoplasm", "Epithelial tumor of thymus", "thymic epithelial neoplasm", "Thymic Epithelial Neoplasm", "Thymus Epithelial Neoplasm", "Thymus epithelial neoplasm", "Epithelial Tumor of Thymus", "epithelial tumor of Thymus", "thymic epithelium neoplasm", "epithelial neoplasm of Thymus", "Epithelial Neoplasm of Thymus", "epithelial tumor of the Thymus", "Epithelial Tumor of the Thymus", "Epithelial Neoplasm of the Thymus", "epithelial neoplasm of the Thymus", "Thymic epithelial neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thymic epithelial neoplasm", "shortest_name_length": 3}
{"curie": "MONDO:0019226", "names": ["glucose transport disorder", "inborn error of glucose transport", "rare inborn error of glucose transport"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glucose transport disorder", "shortest_name_length": 26}
{"curie": "MONDO:0004151", "names": ["spinal meninges cancer", "meninx of spinal cord cancer", "cancer of meninx of spinal cord", "malignant tumor of spinal meninges", "malignant neoplasm of spinal meninges", "Malignant neoplasm of spinal meninges", "malignant meninx of spinal cord neoplasm", "malignant neoplasm of meninx of spinal cord", "Malignant neoplasm of spinal meninges (disorder)", "malignant neoplasm of spinal meninges (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal meninges cancer", "shortest_name_length": 22}
{"curie": "UMLS:C4049169", "names": ["Pseudocirrhosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pseudocirrhosis", "shortest_name_length": 15}
{"curie": "UMLS:C2987197", "names": ["Pancreatic IOPN", "Intraductal papillary-mucinous adenoma", "Pancreatic Intraductal Oncocytic Papillary Neoplasm", "Pancreatic Intraductal Papillary Mucinous Neoplasm, Oncocytic-Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Intraductal Papillary Mucinous Neoplasm, Oncocytic-Type", "shortest_name_length": 15}
{"curie": "MONDO:0015748", "names": ["White sponge nevus", "white sponge nevus", "white sponge; nevus", "White sponge naevus", "White folded stomatitis", "Hereditary leukokeratosis", "Hereditary oral keratosis", "Leucokeratosis mucosae oris", "Leukokeratosis mucosae oris", "WHITE SPONGE NEVUS OF CANNON", "White Sponge Nevus of Cannon", "White sponge nevus of mucosa", "White sponge nevus of Cannon", "white sponge nevus of Cannon", "Leukokeratosis of oral mucosa", "Hereditary white sponge nevus", "White sponge naevus of mucosa", "White folded gingivostomatosis", "Hereditary white sponge naevus", "White folded gingivo-stomatosis", "hereditary mucosal leukokeratosis", "Hereditary mucosal leukokeratosis", "Hereditary Mucosal Leukokeratoses", "Hereditary Mucosal Leukokeratosis", "Mucosal Leukokeratosis, Hereditary", "Mucosal Leukokeratoses, Hereditary", "Leukokeratosis, Hereditary Mucosal", "Leukokeratoses, Hereditary Mucosal", "LEUKOKERATOSIS, HEREDITARY MUCOSAL", "Hereditary leukokeratosis of mucosa", "Familial white folded mucosal dysplasia", "White sponge nevus of mucosa (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary mucosal leukokeratosis", "shortest_name_length": 18}
{"curie": "MONDO:0000966", "names": ["PL", "pleomorphic lipoma", "Pleomorphic Lipoma", "Pleomorphic lipoma", "lipoma pleomorphic", "Pleomorphic Lipomas", "pleomorphic; lipoma", "lipoma; pleomorphic", "Lipoma, Pleomorphic", "Lipomas, Pleomorphic", "[M] Pleomorphic lipoma", "Pleomorphic lipoma (disorder)", "Pleomorphic lipoma (morphologic abnormality)", "pleomorphic lipoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pleomorphic lipoma", "shortest_name_length": 2}
{"curie": "MONDO:0012960", "names": ["MRD5", "SYNGAP1 syndrome", "SYNGAP1-related NSID", "autosomal dominant mental retardation 5", "mental retardation, autosomal dominant 5", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 5", "Mental Retardation, Autosomal Dominant 5", "autosomal dominant intellectual disability 5", "intellectual disability, autosomal dominant 5", "mental retardation, autosomal dominant type 5", "intellectual disability, autosomal dominant type 5", "SYNGAP1-related non-syndromic intellectual disability", "autosomal dominant intellectual developmental disorder 5", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5", "autosomal dominant non-syndromic intellectual disability 5", "SYNGAP1 autosomal dominant non-syndromic intellectual disability", "SYNGAP1 Gene mutation linked to intellectual disability, schizophrenia and autism", "autosomal dominant non-syndromic intellectual disability caused by mutation in SYNGAP1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 5", "shortest_name_length": 4}
{"curie": "MONDO:0003287", "names": ["leiomyoma of CNS", "Leiomyoma of CNS", "leiomyoma of the CNS", "Leiomyoma of the CNS", "central nervous system leiomyoma", "Central Nervous System Leiomyoma", "leiomyoma of central nervous system", "Leiomyoma of Central Nervous System", "leiomyoma of the central nervous system", "Leiomyoma of the Central Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system leiomyoma", "shortest_name_length": 16}
{"curie": "UMLS:C0085654", "names": ["INJECTION SITE GRANULOMA", "Injection site granuloma", "GRANULOMA INJECTION SITE", "Granuloma injection site", "Injection site granuloma, NOS", "Injection site granuloma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site granuloma", "shortest_name_length": 24}
{"curie": "MONDO:0023704", "names": ["Martinez Monasterio Pinheiro syndrome", "cleft lip/palate oligodontia syndactyly hair alterations", "Cleft lip-palate-oligodontia-syndactyly-hair alterations", "cleft lip-palate-oligodontia-syndactyly-hair alterations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Martinez Monasterio Pinheiro syndrome", "shortest_name_length": 37}
{"curie": "UMLS:C0392617", "names": ["PSEUDONEUROMA", "pseudoneuroma", "Amputation Neuroma", "Amputation neuroma", "amputation neuroma", "neuroma amputation", "amputation; neuroma", "neuroma; amputation", "NEUROMA, AMPUTATION", "neuroma; amputation stump", "amputation stump; neuroma", "Neuroma of amputation stump", "amputation neuroma (diagnosis)", "Neuroma of amputation stump (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neuroma of amputation stump", "shortest_name_length": 13}
{"curie": "UMLS:C1096347", "names": ["gastric sarcoma", "Gastric Sarcoma", "Gastric sarcoma", "sarcoma of stomach", "sarcoma of stomach (diagnosis)", "Malignant Gastric Soft Tissue Neoplasm", "Malignant Soft Tissue Neoplasm of Stomach", "Malignant Soft Tissue Neoplasm of the Stomach"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric sarcoma", "shortest_name_length": 15}
{"curie": "MONDO:0022919", "names": ["cytokine receptor deficiency", "cytokine receptor activity disease", "disorder of cytokine receptor activity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cytokine receptor deficiency", "shortest_name_length": 28}
{"curie": "MONDO:0019309", "names": ["JEB-lo", "Late-onset JEB", "EB progressive", "Epidermolysis bullosa progressiva", "late-onset junctional epidermolysis bullosa", "Late-onset junctional epidermolysis bullosa", "Late-onset junctional epidermolysis bullosa (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "late-onset junctional epidermolysis bullosa", "shortest_name_length": 6}
{"curie": "MONDO:0015402", "names": ["mandibular arteriovenous malformation", "Mandibular arteriovenous malformation", "Arteriovenous malformation of mandible", "arteriovenous malformation of mandible", "Arteriovenous malformation of mandible (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mandibular arteriovenous malformation", "shortest_name_length": 37}
{"curie": "MONDO:0022037", "names": ["Immunoblastoma", "Immunoblastomas", "Immunoblastic Sarcoma", "Immunoblastic sarcoma", "immunoblastic sarcoma", "sarcoma; immunoblastic", "immunoblastic lymphoma", "immunoblastic; sarcoma", "plasmablastic lymphoma", "Immunoblastic Sarcomas", "Immunoblastic lymphoma", "Sarcoma, Immunoblastic", "Immunoblastic Lymphoma", "Sarcomas, Immunoblastic", "lymphoma; immunoblastic", "immunoblastic; lymphoma", "Immunoblastic lymphosarcoma", "LARGE IMMUNOBLASTIC LYMPHOMA", "LYMPHOMA LARGE IMMUNOBLASTIC", "IMMUNOBLASTIC LARGE LYMPHOMA", "LYMPHOMA IMMUNOBLASTIC LARGE", "large cell immunoblastic lymphoma", "Immunoblastic Large Cell Lymphoma", "Large cell immunoblastic lymphoma", "large-cell immunoblastic lymphoma", "Large-Cell Immunoblastic Lymphoma", "Immunoblastic Large-Cell Lymphoma", "Large Cell Immunoblastic Lymphoma", "Lymphoma, Large-Cell Immunoblastic", "Malignant lymphoma - immunoblastic", "Immunoblastic Lymphoma, Large-Cell", "Immunoblastic Large-Cell Lymphomas", "Lymphoma, Immunoblastic Large-Cell", "LYMPHOMA, IMMUNOBLASTIC, MALIGNANT", "Large-Cell Lymphoma, Immunoblastic", "Large-Cell Immunoblastic Lymphomas", "Large-Cell Lymphomas, Immunoblastic", "Diffuse Immunoblastic Lymphosarcoma", "Lymphomas, Immunoblastic Large-Cell", "Lymphoma, immunoblastic, high grade", "Immunoblastic Lymphomas, Large-Cell", "Lymphoma, Large-Cell, Immunoblastic", "Lymphoma, Immunoblastic, Large Cell", "Lymphomas, Large-Cell Immunoblastic", "Lymphoma, Immunoblastic, Large-Cell", "Lymphoma, Large Cell, Immunoblastic", "Diffuse Immunoblastic Lymphosarcomas", "Immunoblastic Lymphosarcoma, Diffuse", "Lymphosarcoma, Diffuse Immunoblastic", "Malignant lymphoma, immunoblastic NOS", "Immunoblastic Lymphosarcomas, Diffuse", "Lymphosarcomas, Diffuse Immunoblastic", "Malignant lymphoma, immunoblastic, NOS", "Malignant lymphoma, immunoblastic type", "[M]Malignant lymphoma, immunoblastic type", "Diffuse non-Hodgkin lymphoma, immunoblastic", "large cell immunoblastic lymphoma (diagnosis)", "Diffuse non-Hodgkin's lymphoma, immunoblastic", "Immunoblastic malignant lymphoma - large cell", "Malignant lymphoma, large cell, immunoblastic", "Immunoblastic (diffuse) non-Hodgkin's lymphoma", "Diffuse non-Hodgkin's immunoblastic (diffuse) lymphoma", "Diffuse non-Hodgkin's lymphoma, immunoblastic (disorder)", "Diffuse non-Hodgkin's lymphoma, immunoblastic (clinical)", "Diffuse non-Hodgkin's lymphoma, immunoblastic (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "large-cell immunoblastic lymphoma", "shortest_name_length": 14}
{"curie": "MONDO:0004580", "names": ["degeneration retina", "Retina degeneration", "retina degeneration", "RETINA DEGENERATION", "Retinal degeneration", "RETINAL DEGENERATION", "degeneration; retina", "retina; degeneration", "retinal degeneration", "DEGENERATION RETINAL", "Degeneration retinal", "degeneration retinal", "Retinal Degeneration", "retinal degenerations", "Degeneration, Retinal", "Retinal Degenerations", "Degeneration of retina", "degeneration of retina", "Degenerations, Retinal", "retina, Degeneration Of", "Retinal degeneration, NOS", "Degeneration of retina, NOS", "retinal degeneration (diagnosis)", "Degeneration of retina (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal degeneration", "shortest_name_length": 19}
{"curie": "MONDO:0002414", "names": ["gastric angioma", "Gastric Angioma", "Gastric Hemangioma", "gastric hemangioma", "angioma of stomach", "stomach hemangioma", "Gastric hemangioma", "Angioma of Stomach", "Gastric haemangioma", "Hemangioma of Stomach", "hemangioma of stomach", "Angioma of the Stomach", "angioma of the stomach", "Hemangioma of the Stomach", "hemangioma of the stomach"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric hemangioma", "shortest_name_length": 15}
{"curie": "MONDO:0032740", "names": ["DFNB100", "autosomal recessive deafness 100", "DEAFNESS, AUTOSOMAL RECESSIVE 100", "deafness, autosomal recessive 100", "hearing loss, autosomal recessive 100", "autosomal recessive nonsyndromic deafness 100"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal recessive 100", "shortest_name_length": 7}
{"curie": "UMLS:C4682625", "names": ["Stage IIIA2 Ovarian Cancer", "Stage IIIA2 Ovarian Cancer AJCC v8", "Stage IIIA2 Ovarian Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA2 Ovarian Cancer AJCC v8", "shortest_name_length": 26}
{"curie": "UMLS:C0393761", "names": ["night wake", "night wakes", "night waking", "Broken sleep", "Night waking", "waking night", "Fitful sleep", "fitful sleep", "Middle Insomnia", "Middle insomnia", "Keeps waking up", "middle insomnia", "interrupted sleep", "Interrupted sleep", "interrupting sleep", "Nocturnal awakening", "Difficulty staying asleep", "Middle insomnia (disorder)", "Sleep maintenance insomnia", "Difficulty in sleep maintenance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Middle insomnia", "shortest_name_length": 10}
{"curie": "MONDO:0007294", "names": ["Cco", "CCD", "CCO", "CNMDU1", "Shy's disease", "Shy-Magee Syndrome", "Shy Magee Syndrome", "Shy-Magee syndrome", "muscle core disease", "Syndrome, Shy-Magee", "Central Core Disease", "central core disease", "CENTRAL CORE DISEASE", "Central core disease", "disease; central core", "Central Core Diseases", "central core myopathy", "Central core myopathy", "Central Core Myopathy", "central core; disease", "myopathy, central core", "Myopathy, Central Core", "congenital myopathy 1A", "Central Core Myopathies", "Myopathies, Central Core", "myopathy, central fibrillar", "muscular central core disease", "CENTRAL CORE DISEASE OF MUSCLE", "central CORE disease of muscle", "Central Core Disease of Muscle", "Central core disease (disorder)", "Central Core Myopathy (disorder)", "central core disease (diagnosis)", "Minicore Myopathy, Moderate, with Hand Involvement", "minicore myopathy, moderate, with hand involvement", "MINICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT", "MULTICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT", "Multicore Myopathy, Moderate, with Hand Involvement", "multicore myopathy, moderate, with hand involvement", "multiminicore disease, moderate, with hand involvement", "NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER", "Neuromuscular Disease, Congenital, With Uniform Type 1 Fiber", "neuromuscular disease, congenital, with uniform type 1 Fiber", "NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central core myopathy", "shortest_name_length": 3}
{"curie": "UMLS:C0160371", "names": ["injury of rectum with open wound into cavity", "Injury to Rectum with Open Wound into Cavity", "Injury to rectum, with open wound into cavity", "injury of rectum with open wound into cavity (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "injury of rectum with open wound into cavity", "shortest_name_length": 44}
{"curie": "MONDO:0000694", "names": ["SAD", "sad", "SADS", "winter depression", "Seasonal depression", "seasonal depression", "seasonal; depression", "depression; seasonal", "Seasonal mood disorder", "Seasonal Mood Disorder", "Disorder, Seasonal Mood", "Mood Disorder, Seasonal", "Seasonal Mood Disorders", "SEASONAL AFFECTIVE DISORDER", "seasonal affective disorder", "Seasonal affective disorder", "seasonal pattern depression", "depression seasonal pattern", "Seasonal Affective Disorder", "Affective Disorder, Seasonal", "Disorder, Seasonal Affective", "Seasonal Affective Disorders", "seasonal affective disorders", "seasonal depression (symptom)", "depression in a seasonal pattern", "seasonal affective disorder (SAD)", "SAD - Seasonal affective disorder", "Seasonal affective disorder (disorder)", "depression seasonal pattern (diagnosis)", "seasonal affective disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "seasonal affective disorder", "shortest_name_length": 3}
{"curie": "UMLS:C5206455", "names": ["Stage IVA Cervical Cancer FIGO 2018", "Stage IVA Cervical Carcinoma FIGO 2018"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Cervical Cancer FIGO 2018", "shortest_name_length": 35}
{"curie": "UMLS:C5670470", "names": ["Supratentorial Ependymoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Supratentorial Ependymoma", "shortest_name_length": 25}
{"curie": "MONDO:0002875", "names": ["ectoparasitism", "infestation; ectoparasite", "ectoparasitic infestation", "Ectoparasitic Infestation", "ectoparasite; infestation", "Infestation, Ectoparasitic", "Ectoparasitic Infestations", "Ectoparasitic infestations", "infestation, ectoparasitic", "Infestations, ectoparasitic", "Infestations, Ectoparasitic", "parasitic ectoparasitic infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parasitic ectoparasitic infectious disease", "shortest_name_length": 14}
{"curie": "UMLS:C1708717", "names": ["Localized Resectable Adult Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized Resectable Adult Hepatocellular Carcinoma", "shortest_name_length": 51}
{"curie": "MONDO:0014683", "names": ["MDDGA9", "congenital muscular dystrophy-dystroglycanopathy type A9", "Walker-Warburg syndrome or muscle-eye-brain disease DAG1-related", "WALKER-WARBURG SYNDROME OR MUSCLE-EYE BRAIN DISEASE, DAG1-RELATED", "Walker-Warburg syndrome or muscle-eye brain disease, Dag1-related", "congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A9", "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A9", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9", "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A9", "shortest_name_length": 6}
{"curie": "UMLS:C4324476", "names": ["Jaw fistula"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jaw fistula", "shortest_name_length": 11}
{"curie": "MONDO:0005678", "names": ["Shipping fever", "Shipping fever of cattle", "Bovine respiratory disease complex", "Bovine Respiratory Disease Complex", "bovine respiratory disease complex", "Bovine respiratory disease complex (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bovine respiratory disease complex", "shortest_name_length": 14}
{"curie": "UMLS:C4524856", "names": ["Refractory Classic Hodgkin Lymphoma", "Refractory Classical Hodgkin Lymphoma", "Classical Hodgkin lymphoma refractory"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Classical Hodgkin lymphoma refractory", "shortest_name_length": 35}
{"curie": "UMLS:C0948298", "names": ["Eardrum hyperemia", "Eardrum hyperaemia", "Tympanic membrane hyperemia", "Tympanic membrane injection", "Tympanic membrane hyperaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tympanic membrane hyperemia", "shortest_name_length": 17}
{"curie": "MONDO:0008590", "names": ["ETM1", "FET1", "essential tremor 1", "DRD3 essential tremor", "Tremor familial essential, 1", "tremor familial essential, 1", "TREMOR, FAMILIAL ESSENTIAL, 1", "tremor, familial essential, 1", "hereditary essential tremor 1", "Tremor, Familial Essential, 1", "tremor hereditary essential, 1", "Tremor hereditary essential, 1", "Tremor, Hereditary Essential, 1", "essential tremor, hereditary, 1", "tremor, hereditary essential, 1", "TREMOR, HEREDITARY ESSENTIAL, 1", "tremor, hereditary essential, type 1", "essential tremor caused by mutation in DRD3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tremor, hereditary essential, 1", "shortest_name_length": 4}
{"curie": "MONDO:0024744", "names": ["choroid plexus neoplasm", "Choroid Plexus Neoplasm", "childhood choroid plexus neoplasm", "Childhood Choroid Plexus Neoplasm", "pediatric choroid plexus neoplasm", "choroid plexus neoplasm of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood choroid plexus neoplasm", "shortest_name_length": 23}
{"curie": "MONDO:0005566", "names": ["NAS", "neonatal withdrawal", "Abstinence Syndrome", "Neonatal Withdrawal Syndrome", "Neonatal Abstinence Syndrome", "neonatal withdrawal syndrome", "neonatal abstinence syndrome", "abstinence neonatal syndrome", "Withdrawal syndrome neonatal", "Neonatal withdrawal syndrome", "Neonatal abstinence syndrome", "WITHDRAWAL SYNDROME NEONATAL", "Neonatal Withdrawal Syndromes", "Syndrome, Neonatal Abstinence", "Neonatal Abstinence Syndromes", "Neonatal Substance Withdrawal", "Abstinence Syndrome, Neonatal", "Withdrawal Syndrome, Neonatal", "Syndrome, Neonatal Withdrawal", "Syndromes, Neonatal Withdrawal", "Abstinence Syndromes, Neonatal", "Syndromes, Neonatal Abstinence", "Withdrawal Syndromes, Neonatal", "Withdrawal, Neonatal Substance", "Neonatal Substance Withdrawals", "Substance Withdrawal, Neonatal", "Substance Withdrawals, Neonatal", "Newborn drug withdrawal syndrome", "neonatal AOD abstinence syndrome", "Neonatal drug withdrawal syndrome", "neonatal drug withdrawal syndrome", "Drug withdrawal syndrome neonatal", "Drug withdrawal syndrome in newborn", "drug withdrawal syndrome in newborn", "neonatal narcotic withdrawal syndrome", "Neonatal Narcotic Withdrawal Syndrome", "Neonatal abstinence syndrome (disorder)", "neonatal drug withdrawal syndrome (diagnosis)", "neonatal Alcohol or Other Drugs abstinence syndrome", "withdrawal; syndrome, drug, infant of dependent mother", "syndrome; withdrawal, drug, infant of dependent mother"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal abstinence syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0002900", "names": ["neuroblastoma of brain", "Cerebral Neuroblastoma", "Neuroblastoma of brain", "cerebral neuroblastoma", "Cerebral neuroblastoma", "neuroblastoma of cerebrum", "neuroblastoma of Cerebrum", "Neuroblastoma of Cerebrum", "telencephalon neuroblastoma", "Cerebral Neuroblastoma, PNET", "cerebral neuroblastoma, PNET", "neuroblastoma of the cerebrum", "Neuroblastoma of the Cerebrum", "neuroblastoma of telencephalon", "malignant neuroblastoma of brain", "Neuroblastoma of brain (disorder)", "Cerebral Hemispheric Neuroblastoma", "cerebral hemispheric neuroblastoma", "Central Nervous System Neuroblastoma", "central nervous system neuroblastoma", "Neuroblastoma of Cerebral Hemispheres", "neuroblastoma of cerebral hemispheres", "neuroblastoma of the cerebral hemisphere", "neuroblastoma of the cerebral hemispheres", "Neuroblastoma of the Cerebral Hemispheres", "malignant neuroblastoma of brain (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral neuroblastoma", "shortest_name_length": 22}
{"curie": "UMLS:C4683011", "names": ["Stage I Eyelid Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Eyelid Carcinoma AJCC v8", "shortest_name_length": 32}
{"curie": "MONDO:0014873", "names": ["NC", "Acne Nevus", "Acne nevus", "acne Nevus", "Acne naevus", "comedo Nevus", "Comedo nevus", "Comedo Nevus", "Comedo naevus", "acneiform Nevus", "Acneiform Nevus", "Acneiform nevus", "Acneiform naevus", "Follicular nevus", "Nevus comedonicus", "NEVUS comedonicus", "Follicular naevus", "NEVUS COMEDONICUS", "Nevus Comedonicus", "Naevus comedonicus", "nevus; comedonicus", "comedonicus; nevus", "nevus comedonicus syndrome", "nevus comedonicus, somatic", "Nevus comedonicus syndrome", "Nevus comedonicus (disorder)", "Pilosebaceous Nevoid Disorder", "pilosebaceous nevoid disorder", "Pilosebaceous nevoid disorder", "Pilosebaceous naevoid disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nevus comedonicus syndrome", "shortest_name_length": 2}
{"curie": "UMLS:C4324487", "names": ["Lymphoid tissue hypoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoid tissue hypoplasia", "shortest_name_length": 26}
{"curie": "MONDO:0000518", "names": ["sacrum chordoma", "Chordoma of sacrum", "Chordoma of sacrum (disorder)", "fused sacrum chordoma (disease)", "chordoma (disease) of fused sacrum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sacrum chordoma", "shortest_name_length": 15}
{"curie": "MONDO:0009600", "names": ["Metaphyseal Dysplasia, Anetoderma, and Optic Atrophy", "metaphyseal dysplasia, anetoderma, and optic atrophy", "METAPHYSEAL DYSPLASIA, ANETODERMA, AND OPTIC ATROPHY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metaphyseal dysplasia, anetoderma, and optic atrophy", "shortest_name_length": 52}
{"curie": "MONDO:0013457", "names": ["LCA15", "Leber congenital amaurosis 15", "LEBER CONGENITAL AMAUROSIS 15", "TULP1 Leber congenital amaurosis", "Leber congenital amaurosis type 15", "retinitis pigmentosa, juvenile, Tulp1-related", "Leber congenital amaurosis caused by mutation in TULP1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leber congenital amaurosis 15", "shortest_name_length": 5}
{"curie": "UMLS:C1112559", "names": ["Pancreatitis due to biliary obstruction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatitis due to biliary obstruction", "shortest_name_length": 39}
{"curie": "MONDO:0020589", "names": ["heart germ cell tumor", "Heart Germ Cell Tumor", "cardiac germ cell tumor", "Cardiac Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiac germ cell tumor", "shortest_name_length": 21}
{"curie": "MONDO:0003467", "names": ["Mediastinal Synovial Sarcoma", "mediastinum synovial sarcoma", "mediastinal synovial sarcoma", "Synovial Sarcoma of Mediastinum", "synovial sarcoma of mediastinum", "Synovial sarcoma of mediastinum", "Synovial Sarcoma of the Mediastinum", "synovial sarcoma of the mediastinum", "mediastinum synovial sarcoma (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mediastinum synovial sarcoma", "shortest_name_length": 28}
{"curie": "MONDO:0019807", "names": ["Mesocardia", "mesocardia", "Midline heart", "mesocardia (disease)", "Mesocardia (disorder)", "Heart in central chest", "mesocardia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mesocardia", "shortest_name_length": 10}
{"curie": "MONDO:0018858", "names": ["Graham Little syndrome", "Piccardi-Lassueur-Little syndrome", "Piccardi Lassueur Little syndrome", "Graham Little-Piccardi-Lassueur syndrome", "Graham-Little-Piccardi-Lassueur syndrome", "Graham Little Piccardi Lassueur syndrome", "Graham Little Piccardi Lassueur syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Graham Little-Piccardi-Lassueur syndrome", "shortest_name_length": 22}
{"curie": "MONDO:0003890", "names": ["invasive bladder urothelial carcinoma", "Invasive bladder Urothelial carcinoma", "Invasive Bladder Urothelial Carcinoma", "infiltrating bladder urothelial carcinoma", "Infiltrating Bladder Urothelial Carcinoma", "invasive bladder transitional cell carcinoma", "Invasive Bladder Transitional Cell Carcinoma", "invasive transitional cell carcinoma of the urinary bladder", "Invasive Transitional Cell Carcinoma of the Urinary Bladder", "Infiltrating Transitional Cell Carcinoma of the Urinary Bladder", "infiltrating transitional cell carcinoma of the urinary bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infiltrating bladder urothelial carcinoma", "shortest_name_length": 37}
{"curie": "UMLS:C5237737", "names": ["Lymphedema of the Head and Neck"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphedema of the Head and Neck", "shortest_name_length": 31}
{"curie": "UMLS:C4525856", "names": ["Stage IIIA Colon Neuroendocrine Tumor", "Stage IIIA Colon Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Colon Neuroendocrine Tumor AJCC v8", "shortest_name_length": 37}
{"curie": "UMLS:C1536526", "names": ["Penile Bowenoid Papulosis", "Bowenoid papulosis of penis", "Bowenoid papulosis of penis (disorder)", "Bowenoid papulosis of penis (diagnosis)", "human papilloma virus-associated neoplasia bowenoid papulosis of penis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bowenoid papulosis of penis", "shortest_name_length": 25}
{"curie": "MONDO:0015416", "names": ["Tessier number 5 facial cleft"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tessier number 5 facial cleft", "shortest_name_length": 29}
{"curie": "MONDO:0014382", "names": ["DOS", "TBRS", "DNMT3A overgrowth syndrome", "Tatton Brown Rahman syndrome", "Tatton-Brown-Rahman syndrome", "TATTON-BROWN-RAHMAN SYNDROME", "TATTON-BROWN-Rahman syndrome", "DNMT3A-related overgrowth syndrome", "Tatton Brown Rahman overgrowth syndrome", "Tatton-Brown-Rahman overgrowth syndrome", "DNA methyltransferase 3 alpha overgrowth syndrome", "tall stature-intellectual disability-facial dysmorphism syndrome", "tall stature, intellectual disability, facial dysmorphism syndrome", "Tall stature, intellectual disability, facial dysmorphism syndrome", "Tall stature, intellectual disability, facial dysmorphism syndrome (disorder)", "tall stature, intellectual disability, facial dysmorphism syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tatton-Brown-Rahman overgrowth syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C0021505", "names": ["Injury to Diaphragm without mention of Open Wound into Cavity", "Injury to diaphragm without mention of open wound into cavity", "Injury to diaphragm, without mention of open wound into cavity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury to diaphragm without mention of open wound into cavity", "shortest_name_length": 61}
{"curie": "MONDO:0011970", "names": ["EPRPDC", "Re-ped-Wc", "RE-PED-WC", "Rolandic epilepsy exercise-induced dystonia", "Rolandic-type focal motor epilepsy and exercise-induced dystonia", "Rolandic epilepsy with paroxysmal exercise-induced dystonia and writer's cramp", "Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome", "rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome", "Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp", "epilepsy, rolandic, with paroxysmal exercise-induce dystonia and writer's cramp", "epilepsy, ROLANDIC, with paroxysmal exercise-induced dystonia and writer'S cramp", "EPILEPSY, ROLANDIC, WITH PAROXYSMAL EXERCISE-INDUCED DYSTONIA AND WRITER'S CRAMP", "Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome", "Epilepsy, Rolandic, With Paroxysmal Exercise-Induced Dystonia And Writer's Cramp", "Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C0281703", "names": ["Stage II Large Cell Lymphoma", "stage II childhood large cell lymphoma", "Pediatric Large Cell Lymphoma Stage II", "Childhood Large Cell Lymphoma Stage II", "Stage II Pediatric Large Cell Lymphoma", "Stage II Childhood Large Cell Lymphoma", "childhood large cell lymphoma, stage II", "pediatric large cell lymphoma, stage II", "lymphoma, stage II childhood large cell", "stage II large cell lymphoma, childhood", "large cell lymphoma, childhood, stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Childhood Large Cell Lymphoma", "shortest_name_length": 28}
{"curie": "UMLS:C1333952", "names": ["Helicobacter Pylori-Associated Gastric MALT", "Helicobacter Pylori-Associated Gastric Mucosa-Associated Lymphoid Tissue Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Helicobacter Pylori-Associated Gastric Mucosa-Associated Lymphoid Tissue Lymphoma", "shortest_name_length": 43}
{"curie": "UMLS:C2243080", "names": ["NECROSIS BOWEL", "Necrosis bowel", "bowel necrosis", "necrosis; bowel", "bowel; necrosis", "intestine necrosis", "necrosis intestine", "NECROSIS INTESTINAL", "intestinal necrosis", "Intestinal necrosis", "INTESTINAL NECROSIS", "intestines necrosis", "Necrosis intestinal", "necrosis of intestine", "Necrosis of intestine", "Necrosis of intestine (disorder)", "necrosis of intestine (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal necrosis", "shortest_name_length": 14}
{"curie": "MONDO:0100061", "names": ["PRPS1 deficiency disorder", "PRPS1-related CMTX5/Arts syndrome/XLNSHL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PRPS1 deficiency disorder", "shortest_name_length": 25}
{"curie": "UMLS:C4053907", "names": ["Type B Tylosis", "Early Onset Tylosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Type B Tylosis", "shortest_name_length": 14}
{"curie": "UMLS:C4682963", "names": ["Urethral Cancer by AJCC v8 Stage", "Urethral Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urethral Cancer by AJCC v8 Stage", "shortest_name_length": 32}
{"curie": "MONDO:0018358", "names": ["neonatal AHA", "neonatal AIHA", "neonatal autoimmune hemolytic anemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal autoimmune hemolytic anemia", "shortest_name_length": 12}
{"curie": "UMLS:C4682802", "names": ["Stage IS Testicular Cancer", "Stage IS Testicular Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IS Testicular Cancer AJCC v8", "shortest_name_length": 26}
{"curie": "MONDO:0021322", "names": ["meningeal cancer", "Meningeal Cancer", "Meninges--Cancer", "Cancer, Meningeal", "Meningeal Cancers", "Cancer of Meninges", "cancer of meninges", "Cancers, Meningeal", "Cancer of the Meninges", "cancer of the meninges", "Neoplasm malig;meninges", "Malignant Meninges Tumor", "meningeal cluster cancer", "malignant meninges tumor", "Malignant Meningeal Tumor", "malignant meningeal tumor", "Malignant Meninges Neoplasm", "malignant meninges neoplasm", "Malignant Tumor of Meninges", "malignant tumor of meninges", "Meningeal Tumors, Malignant", "meningeal tumors, malignant", "Malignant tumor of meninges", "cancer of meningeal cluster", "Malignant tumour of meninges", "Malignant meningeal neoplasm", "Malignant Meningeal Neoplasm", "Malignant Meningeal Neoplasms", "malignant meningeal neoplasms", "Neoplasm, Malignant Meningeal", "Meningeal Neoplasm, Malignant", "malignant neoplasm of meninges", "Meningeal Neoplasms, Malignant", "Malignant neoplasm of meninges", "Malignant Neoplasm of Meninges", "Neoplasms, Malignant Meningeal", "malignant neoplasms of meninges", "Malignant Tumor of the Meninges", "Malignant Neoplasms of Meninges", "malignant tumor of the meninges", "malignant neoplasm of the meninges", "Malignant Neoplasm of the Meninges", "Malignant neoplasm of meninges NOS", "malignant neosplasm of the meninges", "malignant meningeal cluster neoplasm", "Malignant tumor of meninges (disorder)", "malignant neoplasm of meningeal cluster", "malignant neoplasm of meninges (diagnosis)", "Malignant neoplasm of meninges, unspecified", "Malignant meningeal neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant tumor of meninges", "shortest_name_length": 16}
{"curie": "MONDO:0003295", "names": ["leiomyomatosis", "LEIOMYOMATOSIS", "Leiomyomatosis", "Leiomyomatoses", "Leiomyomatosis NOS", "Leiomyomatosis, NOS", "Intravascular leiomyomatosis", "leiomyomatosis, no ICD-O subtype", "Leiomyomatosis (morphologic abnormality)", "Intravascular leiomyomatosis (morphologic abnormality)", "leiomyomatosis, no ICD-O subtype (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leiomyomatosis", "shortest_name_length": 14}
{"curie": "UMLS:C0239161", "names": ["dactylitis", "Dactylitis", "DACTYLITIS", "Dactylitis (disorder)", "dactylitis (diagnosis)", "Painful swelling or discoloration of fingers/toes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dactylitis", "shortest_name_length": 10}
{"curie": "MONDO:0016153", "names": ["qualitative or quantitative defects of TRIM32"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of TRIM32", "shortest_name_length": 45}
{"curie": "MONDO:0004272", "names": ["bladder tuberculous", "Tuberculous cystitis", "tuberculous cystitis", "bladder tuberculosis", "Tuberculosis bladder", "tuberculosis of bladder", "Tuberculosis of bladder", "TB - Tuberculous cystitis", "urinary bladder tuberculosis", "bladder; tuberculous (etiology)", "Tuberculosis of bladder (disorder)", "tuberculosis of bladder (diagnosis)", "Tuberculosis of bladder, unspecified", "bladder; tuberculous (manifestation)", "tuberculosis of bladder, unspecified examination", "Tuberculosis of bladder, unspecified examination"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urinary bladder tuberculosis", "shortest_name_length": 19}
{"curie": "MONDO:0017857", "names": ["spina bifida-hypospadias syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spina bifida-hypospadias syndrome", "shortest_name_length": 33}
{"curie": "UMLS:C4525350", "names": ["IA", "Stage IA Intrahepatic Cholangiocarcinoma AJCC v8", "Stage IA Intrahepatic Bile Duct Cancer (Cholangiocarcinoma)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Intrahepatic Cholangiocarcinoma AJCC v8", "shortest_name_length": 2}
{"curie": "MONDO:0016901", "names": ["Monosomy 2q", "deletion 2q", "2q monosomy", "Deletion 2q", "monosomy 2q", "2q deletion", "2q- syndrome", "del(2q) syndrome", "partial monosomy 2q", "deletion 2q syndrome", "2q deletion syndrome", "chromosome 2q deletion", "chromosome 2q monosomy", "Chromosome 2, monosomy 2q", "chromosome 2q deletion syndrome", "Partial monosomy of chromosome 2q", "Partial deletion of chromosome 2q", "partial monosomy of chromosome 2q", "partial deletion of chromosome 2q", "partial deletion of the long arm of chromosome 2", "Partial monosomy of the long arm of chromosome 2", "partial monosomy of the long arm of chromosome 2", "Partial deletion of the long arm of chromosome 2", "partial deletion of the long arm of chromosome type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of the long arm of chromosome 2", "shortest_name_length": 11}
{"curie": "UMLS:C1335018", "names": ["Non-Neoplastic Laryngeal Disease", "Non-Neoplastic Laryngeal Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Laryngeal Disorder", "shortest_name_length": 32}
{"curie": "MONDO:0030549", "names": ["DFNA81", "deafness, autosomal dominant 81", "DEAFNESS, AUTOSOMAL DOMINANT 81", "hearing loss, autosomal dominant 81"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal dominant 81", "shortest_name_length": 6}
{"curie": "UMLS:C2700204", "names": ["FTCL", "Follicular T-cell lymphoma", "Follicular T-Cell Lymphoma", "Follicular Variant Peripheral T-Cell Lymphoma", "Follicular T-cell lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Follicular T-cell lymphoma", "shortest_name_length": 4}
{"curie": "UMLS:C4525729", "names": ["Cortical Cataract Grade 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cortical Cataract Grade 3", "shortest_name_length": 25}
{"curie": "MONDO:0022697", "names": ["Vogt", "ADCP", "Vogt disease", "Vogt's disease", "Athetoid cerebral palsy", "cerebral palsy athetoid", "athetoid cerebral palsy", "Athetoid Cerebral Palsy", "Cerebral Palsy, Athetoid", "Dyskinetic cerebral palsy", "Dyskinetic Cerebral Palsy", "cerebral palsy dyskinetic", "dyskinetic cerebral palsy", "Cerebral Palsy, Dyskinetic", "Cerebral Palsies, Athetoid", "Cerebral Palsies, Dyskinetic", "paralysis; cerebral, athetoid", "cerebral; paralysis, athetoid", "cerebral; paralysis, dyskinetic", "paralysis; cerebral, dyskinetic", "Athetoid Dyskinetic Cerebral Palsy", "athetoid dyskinetic cerebral palsy", "Athetoid cerebral palsy (disorder)", "athetoid cerebral palsy (diagnosis)", "Dyskinetic cerebral palsy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "athetoid cerebral palsy", "shortest_name_length": 4}
{"curie": "MONDO:0010638", "names": ["Keratosis follicularis dwarfism cerebral atrophy", "keratosis follicularis dwarfism and cerebral atrophy", "KERATOSIS FOLLICULARIS, DWARFISM, AND CEREBRAL ATROPHY", "keratosis follicularis, dwarfism, and cerebral atrophy", "Keratosis Follicularis, Dwarfism, and Cerebral Atrophy", "keratosis follicularis-dwarfism-cerebral atrophy syndrome", "dwarfism, cerebral atrophy and generalized keratosis follicularis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratosis follicularis-dwarfism-cerebral atrophy syndrome", "shortest_name_length": 48}
{"curie": "UMLS:C3273077", "names": ["Liver Germ cell Tumor", "Liver Germ Cell Tumor", "Hepatic Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liver Germ Cell Tumor", "shortest_name_length": 21}
{"curie": "MONDO:0009121", "names": ["DK Phocomelia Syndrome", "DK phocomelia syndrome", "DK PHOCOMELIA SYNDROME", "Von Voss Cherstvoy syndrome", "Von Voss-Cherstvoy syndrome", "von Voss-Cherstvoy syndrome", "VON VOSS-CHERSTVOY SYNDROME", "Von Voss-Cherstvoy Syndrome", "DK phocomelia syndrome (disorder)", "phocomelia, thrombocytopenia, encephalocele, urogenital malformations", "PHOCOMELIA, THROMBOCYTOPENIA, ENCEPHALOCELE, UROGENITAL MALFORMATIONS", "Phocomelia, Thrombocytopenia, Encephalocele, Urogenital Malformations", "phocomelia thrombocytopenia encephalocele and urogenital malformations", "Phocomelia-thrombocytopenia-encephalocele-urogenital malformations syndrome", "phocomelia-thrombocytopenia-encephalocele-urogenital malformations syndrome", "Phocomelia, thrombocytopenia, encephalocele and urogenital malformation syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "von Voss-Cherstvoy syndrome", "shortest_name_length": 22}
{"curie": "MONDO:0004202", "names": ["adrenal medulla carcinoma", "carcinoma of adrenal medulla"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adrenal medulla carcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0016556", "names": ["transient congenital hypothyroidism due to neonatal factor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transient congenital hypothyroidism due to neonatal factor", "shortest_name_length": 58}
{"curie": "MONDO:0006904", "names": ["Phimoses", "phimoses", "PHIMOSIS", "phimosis", "Phimosis", "Tight prepuce", "Tight foreskin", "tight foreskin", "tight frenulum", "Tight frenulum", "Phimosis (disorder)", "phimosis (diagnosis)", "Tight foreskin (finding)", "phimosis (physical finding)", "PREPUTIAL RETRACTION FAILURE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phimosis", "shortest_name_length": 8}
{"curie": "UMLS:C0473391", "names": ["Parabasal Thrombus", "Parabasal Hematoma", "Retroplacental Hematoma", "Retroplacental hematoma", "Retroplacental Thrombus", "retroplacental hematoma", "hematomas retroplacental", "Retroplacental haematoma", "Retroplacental hematoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retroplacental hematoma", "shortest_name_length": 18}
{"curie": "MONDO:0015839", "names": ["double uterus", "UTERUS DOUBLE", "Double uterus", "Septate uterus", "Septate Uterus", "uterus; duplex", "double; uterus", "UTERUS SEPTATE", "septate uterus", "Uterine septum", "Uterine Septum", "duplex; uterus", "uterus; double", "septated uterus", "Uterus, Septate", "Uterus, septate", "doubling uterus", "Uterine Septums", "Septum, Uterine", "Bipartite uterus", "doubling of uterus", "Doubling of uterus", "uterus bilocularis", "Uterus bilocularis", "Septate uterus NOS", "Doubling of uterus NOS", "septate uterus (diagnosis)", "Doubling of uterus any degree", "Uterus bilocularis (disorder)", "uterus bilocularis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "septate uterus", "shortest_name_length": 13}
{"curie": "MONDO:0023208", "names": ["Fuqua Berkovitz syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fuqua Berkovitz syndrome", "shortest_name_length": 24}
{"curie": "UMLS:C0854998", "names": ["Pharyngeal Cancer Stage I", "Pharyngeal cancer stage I", "pharyngeal cancer stage I", "Stage I Pharyngeal Cancer", "Stage I Pharyngeal Throat Cancer", "Pharynx neoplasm malignant stage I", "malignant tumor of pharynx stage I", "Malignant neoplasm of pharynx stage I", "malignant neoplasm of pharynx stage I", "malignant neoplasm of pharynx stage I (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pharyngeal cancer stage I", "shortest_name_length": 25}
{"curie": "MONDO:0015589", "names": ["Limbic Encephalitis", "limbic encephalitis", "encephalitis limbic", "Limbic encephalitis", "Encephalitis, Limbic", "Limbic encephalopathy", "limbic encephalopathy", "Limbic encephalitis (disorder)", "Limbic encephalitis (diagnosis)", "paraneoplastic limbic encephalitis", "Paraneoplastic limbic encephalitis", "Paraneoplastic Limbic Encephalitis", "Limbic Encephalitis, Paraneoplastic", "Encephalitis, Paraneoplastic Limbic", "Paraneoplastic limbic encephalopathy", "paraneoplastic limbic; encephalopathy", "encephalopathy; paraneoplastic limbic", "Encephalitides, Paraneoplastic Limbic", "Paraneoplastic limbic encephalitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paraneoplastic limbic encephalitis", "shortest_name_length": 19}
{"curie": "UMLS:C0854813", "names": ["Refractory Lymphoplasmacytic Lymphoma", "Refractory Lymphoplasmacytoid Lymphoma/Immunocytoma", "Lymphoplasmacytoid lymphoma/immunocytoma refractory"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoplasmacytoid lymphoma/immunocytoma refractory", "shortest_name_length": 37}
{"curie": "UMLS:C5420182", "names": ["Laryngeal Neuroendocrine Carcinoma", "Primary Laryngeal Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laryngeal Neuroendocrine Carcinoma", "shortest_name_length": 34}
{"curie": "UMLS:C0235378", "names": ["hepatotoxicity", "Hepatotoxicity", "HEPATOTOXICITY", "Hepatic Toxicity", "HEPATOTOXIC EFFECT", "Hepatotoxicity NOS", "Hepatotoxic effect", "Hepatotoxicity, NOS", "Toxic effect on liver cells"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatotoxicity", "shortest_name_length": 14}
{"curie": "UMLS:C0496873", "names": ["Benign retroperitoneal tumor", "benign retroperitoneal tumor", "Benign retroperitoneal tumour", "benign retroperitoneal neoplasm", "benign tumor of retroperitoneum", "Benign retroperitoneal neoplasm", "Benign Retroperitoneal Neoplasm", "Benign neoplasm of retroperitoneum", "benign neoplasm of retroperitoneum", "Benign neoplasm of the retroperitoneum", "Benign neoplasm of retroperitoneal tissue", "Benign neoplasm of retroperitoneum (disorder)", "benign neoplasm of retroperitoneum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign neoplasm of retroperitoneum", "shortest_name_length": 28}
{"curie": "UMLS:C0749591", "names": ["tonsillopharyngitis", "Tonsillopharyngitis", "TONSILLOPHARYNGITIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tonsillopharyngitis", "shortest_name_length": 19}
{"curie": "UMLS:C1511264", "names": ["Borderline Ovarian Mucinous Tumor, Endocervical-Like"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Ovarian Mucinous Tumor, Endocervical-Like", "shortest_name_length": 52}
{"curie": "UMLS:C0014324", "names": ["Entamoebosis", "Entamoebiasis", "Entamoebiases", "Entamoeba Infection", "Entamoeba Infections", "Infection, Entamoeba", "Infections, Entamoeba", "Infection by Entamoeba", "Infection by Entamoeba, NOS", "Infection caused by Entamoeba", "Infection caused by Entamoeba (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Entamoebiasis", "shortest_name_length": 12}
{"curie": "MONDO:0049221", "names": ["MYP26", "MYOPIA 26, X-LINKED, FEMALE-LIMITED", "myopia 26, X-linked, female-limited"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopia 26, X-linked, female-limited", "shortest_name_length": 5}
{"curie": "MONDO:0011267", "names": ["Mrst", "MRST", "mental retardation, severe, with spasticity and tapetoretinal degeneration", "MENTAL RETARDATION, SEVERE, WITH SPASTICITY AND PIGMENTARY TAPETORETINAL DEGENERATION", "mental retardation, severe, with spasticity and pigmentary tapetoretinal degeneration", "Mental Retardation, Severe, With Spasticity And Pigmentary Tapetoretinal Degeneration", "intellectual disability, severe, with spasticity and pigmentary tapetoretinal degeneration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, severe, with spasticity and pigmentary tapetoretinal degeneration", "shortest_name_length": 4}
{"curie": "MONDO:0010622", "names": ["sts", "XLI", "STS", "SSDD", "ssdd", "RXLI", "STS deficiency", "STS DEFICIENCY", "X-linked ichthyosis", "ichthyosis x-linked", "X-Linked Ichthyosis", "x linked ichthyosis", "X linked ichthyosis", "x-linked ichthyosis", "Ichthyosis, X Linked", "X-linked; ichthyosis", "ICHTHYOSIS, X-LINKED", "ichthyosis, X-linked", "Ichthyoses, X-Linked", "Ichthyosis, X-Linked", "ichthyosis; X-linked", "Ichthyosis, X-linked", "Sex-linked ichthyosis", "Ichthyosis, Sex-Linked", "Ichthyoses, Sex-Linked", "Ichthyosis, Sex Linked", "Arylsulfatase C deficiency", "Steryl-sulfatase deficiency", "Arylsulphatase C deficiency", "Steroid Sulfatase Deficiency", "STEROID SULFATASE DEFICIENCY", "X-linked ichthyosis syndrome", "Steroid sulfatase deficiency", "steroid sulfatase deficiency", "Recessive X-linked ichthyosis", "x-linked recessive ichthyosis", "Deficiency, Steroid Sulfatase", "Steroid sulphatase deficiency", "X-linked recessive ichthyosis", "Sulfatase Deficiency, Steroid", "recessive X-linked ichthyosis", "Placental sulfatase deficiency", "Steroid Sulfatase Deficiencies", "Deficiency of steryl-sulfatase", "ichthyosis (disease), X-linked", "placental sulfatase deficiency", "Sulfatase Deficiencies, Steroid", "Placental sulphatase deficiency", "Deficiency of steryl-sulphatase", "X-linked ichthyosis (diagnosis)", "Deficiencies, Steroid Sulfatase", "X-linked ichthyosis (STS, SSDD)", "Ichthyosis, sex-linked, recessive", "ichthyosis, X-linked, complicated", "ICHTHYOSIS, X-LINKED, COMPLICATED", "Ichthyosis, X-Linked, Complicated", "XRI - X-linked recessive ichthyosis", "Steroid sulfatase deficiency disease", "steroid sulfatase deficiency disease", "STEROID SULFATASE DEFICIENCY DISEASE", "Steroid Sulfatase Deficiency Disease", "placental steroid sulfatase deficiency", "Placental Steroid Sulfatase Deficiency", "PLACENTAL STEROID SULFATASE DEFICIENCY", "Placental steroidal sulfatase deficiency", "Steryl-sulfate sulfohydrolase deficiency", "placental disorders deficiency sulfatase", "ichthyosis , X-linked, X-linked recessive", "Placental steroidal sulphatase deficiency", "Steryl-sulphate sulphohydrolase deficiency", "Placental sulfatase deficiency (diagnosis)", "X-linked placental steryl-sulfatase deficiency", "X-linked placental steryl-sulphatase deficiency", "X-linked ichthyosis with steryl-sulfatase deficiency", "ichthyosis x-linked with steryl-sulfatase deficiency", "X-linked ichthyosis with steryl-sulphatase deficiency", "Disorder involving deficiency of steryl-sulfatase (EC 3.1.6.2)", "X-linked ichthyosis with steryl-sulfatase deficiency (disorder)", "X-linked ichthyosis with steryl-sulfatase deficiency (diagnosis)", "Disorder involving deficiency of steryl-sulfatase (EC 3.1.6.2) (disorder)", "Placental sulfatase deficiency (X-linked steryl-sulfatase deficiency) in a female", "Placental sulfatase deficiency (X-linked steryl-sulfatase deficiency) in a female (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "recessive X-linked ichthyosis", "shortest_name_length": 3}
{"curie": "MONDO:0017509", "names": ["adactyly of foot, unilateral", "congenital absence of toes, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adactyly of foot, unilateral", "shortest_name_length": 28}
{"curie": "MONDO:0012701", "names": ["CTRCT12", "cataract 12 multiple types", "cataract 12, multiple types", "CATARACT 12, MULTIPLE TYPES", "Cataract, Autosomal Dominant, Multiple Types 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 12 multiple types", "shortest_name_length": 7}
{"curie": "MONDO:0001150", "names": ["Hydrocephaly", "hydrocephaly", "HYDROCEPHALUS", "Hydrencephaly", "hydrocephalus", "Hydrocephalus", "hydrencephaly", "Hydrencephalus", "hydrencephalus", "Hydrocephalus NOS", "Water on the brain", "hydrocephalus, X-linked", "Hydrocephalus (disorder)", "hydrocephalus (diagnosis)", "Hydrocephalus, unspecified", "Nonsyndromal hydrocephalus", "Too much cerebrospinal fluid in the brain", "hydrocephalus, nonsyndromic, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hydrocephalus", "shortest_name_length": 12}
{"curie": "UMLS:C5419783", "names": ["Colorectal Conventional Adenoma", "Conventional Colorectal Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Conventional Adenoma", "shortest_name_length": 31}
{"curie": "MONDO:0005494", "names": ["Triple negative breast cancer", "triple-negative breast cancer", "Triple-negative breast cancer", "Triple Negative Breast Cancer", "Triple-Negative Breast Cancer", "Breast Cancer, Triple-Negative", "Triple-Negative Breast Cancers", "Triple Negative Breast Neoplasm", "Triple-Negative Breast Neoplasm", "Breast Cancers, Triple-Negative", "Triple-Negative Breast Neoplasms", "Triple Negative Breast Neoplasms", "Triple-Negative Breast Carcinoma", "triple-negative breast carcinoma", "Breast Neoplasm, Triple-Negative", "Breast Neoplasms, Triple-Negative", "TNBC - Triple-negative breast cancer", "triple-receptor negative breast cancer", "Triple negative breast cancer metastatic", "Triple negative malignant neoplasm of breast", "ER-Negative PR-Negative HER2-Negative Breast Cancer", "ER Negative PR Negative HER2 Negative Breast Cancer", "ER-Negative PR-Negative HER2-Negative Breast Neoplasms", "ER Negative PR Negative HER2 Negative Breast Neoplasms", "hormone receptor negative malignant tumor breast triple", "Triple negative malignant neoplasm of breast (disorder)", "Triple negative malignant neoplasm of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "triple-negative breast carcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0024653", "names": ["Skull Tumor", "skull tumor", "Tumor of Skull", "Skull Neoplasm", "skull neoplasm", "tumor of skull", "Skull Neoplasms", "Neoplasm, Skull", "Neoplasms, Skull", "neoplasm of skull", "Neoplasm of Skull", "Tumor of the Skull", "tumor of the skull", "Neoplasm of the Skull", "neoplasm of the skull", "Neoplasm of bone of skull", "neoplasm of skull (diagnosis)", "Neoplasm of bone of skull (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skull neoplasm", "shortest_name_length": 11}
{"curie": "MONDO:0015997", "names": ["noble Bass Sherman syndrome", "noble-Bass-Sherman syndrome", "Noble-Bass-Sherman syndrome", "Noble Bass Sherman syndrome", "ectopia lentis chorioretinal dystrophy myopia", "Ectopia lentis chorioretinal dystrophy myopia", "Ectopia lentis-chorioretinal dystrophy-myopia syndrome", "ectopia lentis-chorioretinal dystrophy-myopia syndrome", "Ectopia lentis, chorioretinal dystrophy, myopia syndrome", "Ectopia lentis, chorioretinal dystrophy, myopia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectopia lentis-chorioretinal dystrophy-myopia syndrome", "shortest_name_length": 27}
{"curie": "UMLS:C4721747", "names": ["Stage IV Esophageal Squamous Cell Cancer", "Stage IV Esophagus Squamous Cell Carcinoma", "Stage IV Esophageal Squamous Cell Carcinoma", "Esophageal Squamous Cell Carcinoma Stage IV", "Stage IV Squamous Cell Carcinoma of Esophagus", "Stage IV Squamous Cell Carcinoma of the Esophagus", "Stage IV Esophageal Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Esophageal Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 40}
{"curie": "MONDO:0012871", "names": ["Jlns2", "JLNS2", "JERVELL AND LANGE-NIELSEN SYNDROME 2", "Jervell and Lange-Nielsen syndrome 2", "Jervell And Lange-Nielsen Syndrome 2", "KCNE1 Jervell and Lange-Nielsen syndrome", "Jervell and Lange-Nielsen syndrome type 2", "JERVELL AND LANGE-NIELSEN SYNDROME 2 (disorder)", "Jervell and Lange-Nielsen syndrome caused by mutation in KCNE1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jervell and Lange-Nielsen syndrome 2", "shortest_name_length": 5}
{"curie": "MONDO:0001277", "names": ["Cerebral arteritis", "cerebral arteritis", "cerebral; arteritis", "arteritis; cerebral", "cerebral artery inflammation", "Cerebral arteritis (disorder)", "cerebral arteritis (diagnosis)", "inflammation of cerebral artery"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral arteritis", "shortest_name_length": 18}
{"curie": "MONDO:0004780", "names": ["strictly posterior acute myocardial infarction", "True posterior wall infarction, episode of care unspecified", "Acute myocardial infarction, true posterior wall infarction, episode of care unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "strictly posterior acute myocardial infarction", "shortest_name_length": 46}
{"curie": "UMLS:C4521631", "names": ["Stage II Laryngeal Throat Cancer", "Stage II Laryngeal Cancer AJCC v8", "Stage II Laryngeal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Laryngeal Cancer AJCC v8", "shortest_name_length": 32}
{"curie": "UMLS:C1334854", "names": ["Myxoid Chondrosarcoma NCI Grade 1", "Myxoid Chondrosarcoma NCI Grade I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myxoid Chondrosarcoma NCI Grade 1", "shortest_name_length": 33}
{"curie": "MONDO:0001748", "names": ["maxillary sinus cancer", "Maxillary Sinus Cancer", "maxillary sinus carcinoma", "cancer of maxillary sinus", "Maxillary Sinus Carcinoma", "Cancer of maxillary antrum", "SINUS, MAXILLARY, CARCINOMA", "Malignant neoplasm of antrum", "malignant neoplasm of antrum", "carcinoma of maxillary sinus", "Malignant Maxillary Sinus Tumor", "malignant maxillary sinus tumor", "Malignant tumor of maxillary sinus", "malignant maxillary sinus neoplasm", "malignant tumor of maxillary sinus", "Malignant Tumor of Maxillary Sinus", "Malignant Maxillary Sinus Neoplasm", "SINUS, MAXILLARY, CANCER, CARCINOMA", "Malignant tumour of maxillary sinus", "Malignant tumor of maxillary antrum", "Malignant tumour of maxillary antrum", "malignant neoplasm of maxillary sinus", "Malignant Neoplasm of Maxillary Sinus", "Malignant neoplasm of maxillary sinus", "Malignant neoplasm of maxillary antrum", "Malignant Tumor of the Maxillary Sinus", "malignant tumor of the maxillary sinus", "Malignant neoplasm of antrum of Highmore", "carcinoma of maxillary sinus (diagnosis)", "Malignant Neoplasm of the Maxillary Sinus", "malignant neoplasm of the maxillary sinus", "Malignant tumor of maxillary sinus (disorder)", "malignant neoplasm of maxillary sinus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maxillary sinus carcinoma", "shortest_name_length": 22}
{"curie": "MONDO:0007516", "names": ["EEC syndrome without cleft Lip/palate", "EEC SYNDROME WITHOUT CLEFT LIP/PALATE", "ectrodactyly-ectodermal dysplasia without clefting syndrome", "ECTRODACTYLY AND ECTODERMAL DYSPLASIA WITHOUT CLEFT LIP/PALATE", "ectrodactyly and ectodermal dysplasia without cleft lip/palate", "Ectrodactyly and Ectodermal Dysplasia without Cleft Lip-Palate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectrodactyly and ectodermal dysplasia without cleft lip/palate", "shortest_name_length": 37}
{"curie": "UMLS:C1332521", "names": ["Benign Non-Epithelial Liver Neoplasm", "Benign Non-Epithelial Hepatic Neoplasm", "Benign Non-Epithelial Liver and Intrahepatic Bile Duct Neoplasm", "Liver and Intrahepatic Bile Duct Benign Non-Epithelial Neoplasm", "Benign Non-Epithelial Hepatic and Intrahepatic Bile Duct Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liver and Intrahepatic Bile Duct Benign Non-Epithelial Neoplasm", "shortest_name_length": 36}
{"curie": "MONDO:0033980", "names": ["RELA fusion-positive ependymoma", "Ependymoma, RELA Fusion-Positive", "Ependymoma, RELA fusion-positive", "Ependymoma, ZFTA-RELA Fusion-Positive", "Supratentorial C11ORF95-RELA fused ependymoma", "Supratentorial Ependymoma, RELA Fusion-Positive", "C11orf95 fusion-positive supratentorial ependymoma", "Supratentorial Ependymoma, ZFTA-RELA Fusion-Positive", "RELA fusion-positive ependymoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "RELA fusion-positive ependymoma", "shortest_name_length": 31}
{"curie": "UMLS:C0679392", "names": ["aseptic necrosis femur", "FEMUR NECROSIS ASEPTIC", "femur necrosis avascular", "FEMUR NECROSIS AVASCULAR", "avascular necrosis femur", "avascular femur necrosis", "Aseptic necrosis of femur", "aseptic necrosis of femur", "Avascular Necrosis of Femur", "Aseptic necrosis of femur NOS", "aseptic necrosis of femur (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aseptic necrosis of femur", "shortest_name_length": 22}
{"curie": "MONDO:0100250", "names": ["SRXX1", "ovotesticular DSD", "46,XX Sex Reversal 1", "46,XX sex reversal 1", "46,XX SEX reversal 1", "XX Male, SRY-Positive", "46,XX Sex reversal type 1", "46,XX Sex reversal, SRY-positive", "46XX sex reversal 1, X-linked dominant", "46,XX true hermaphroditism, SRY-positive", "ovotesticular disorder of sex development", "46,XX gonadal dysgenesis, complete, SRY-positive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XX sex reversal 1", "shortest_name_length": 5}
{"curie": "MONDO:0001068", "names": ["osteomalacia", "OSTEOMALACIA", "Osteomalacia", "malacia; bone", "Adult rickets", "adult rickets", "Adult Rickets", "Rickets, Adult", "adults rickets", "OM - Osteomalacia", "OM - osteomalacia", "osteomalacia (disease)", "Softening of the bones", "Osteomalacia (disorder)", "osteomalacia (diagnosis)", "Osteomalacia, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteomalacia", "shortest_name_length": 12}
{"curie": "MONDO:0007631", "names": ["FRA16E", "Fragile Site 16p12", "FRAGILE SITE 16p12", "fragile site 16P12", "chromosome 16p12.1 deletion syndrome", "Chromosome 16p12.1 Deletion Syndrome", "chromosome 16p12.1 deletion syndrome, 520kb", "chromosome 16p12.1 deletion syndrome, 520-KB", "Chromosome 16p12.1 Deletion Syndrome, 520-KB", "CHROMOSOME 16p12.1 DELETION SYNDROME, 520-KB", "chromosome 16p12.1 deletion syndrome, type 520kb", "fragile site, Distamycin a type, Rare, fra(16)(p12.1)", "FRAGILE SITE, DISTAMYCIN A TYPE, RARE, FRA(16)(p12.1)", "Recurrent 16p12.1 microdeletion (neurodevelopmental susceptibility locus)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 16p12.1 deletion syndrome, 520kb", "shortest_name_length": 6}
{"curie": "MONDO:0020557", "names": ["pleuropulmonary blastoma type 3", "type III pleuropulmonary blastoma", "Type III Pleuropulmonary Blastoma", "Pleuropulmonary blastoma type III", "Pleuro-pulmonary blastoma type III", "Pleuropulmonary blastoma type III (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pleuropulmonary blastoma type 3", "shortest_name_length": 31}
{"curie": "MONDO:0700181", "names": ["feline fibrosarcoma", "Feline Fibrosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "feline fibrosarcoma", "shortest_name_length": 19}
{"curie": "UMLS:C4727150", "names": ["Refractory Severe Aplastic Anemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Severe Aplastic Anemia", "shortest_name_length": 33}
{"curie": "UMLS:C0274860", "names": ["Organic mercury poisoning", "Organic Mercury Poisoning", "Mercury Poisoning, Organic", "Poisoning, Organic Mercury", "Organic mercury poisoning (disorder)", "Organic mercury compound causing toxic effect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mercury Poisoning, Organic", "shortest_name_length": 25}
{"curie": "UMLS:C0333881", "names": ["Mild Glandular Cell Atypia", "Mild glandular cell atypia", "Mild glandular cell atypia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mild glandular cell atypia", "shortest_name_length": 26}
{"curie": "MONDO:0014250", "names": ["HPRL", "hyperprolactinemia", "familial hyperprolactinemia", "Familial hyperprolactinemia", "Familial hyperprolactinaemia", "Familial hyperprolactinemia (disorder)", "hereditary hyperprolactinemia (disease)", "familial isolated prolactin receptor deficiency", "Familial isolated prolactin receptor deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial hyperprolactinemia", "shortest_name_length": 4}
{"curie": "MONDO:0021451", "names": ["benign brain tumor", "brain tumor benign", "Benign brain tumor", "benign tumor brain", "Benign Brain Tumor", "benign brain tumors", "Benign brain tumour", "benign brain tumour", "benign tumor of brain", "BRAIN NEOPLASM BENIGN", "Benign Brain Neoplasm", "Benign Tumor of Brain", "benign neoplasm brain", "brain benign neoplasm", "Neoplasm benign;brain", "benign brain neoplasm", "Brain Benign Neoplasm", "Brain neoplasm benign", "Benign Brain Neoplasms", "Brain Neoplasm, Benign", "Benign Neoplasm, Brain", "Brain Benign Neoplasms", "Benign Neoplasms, Brain", "brain neoplasms, benign", "Brain Neoplasms, Benign", "Benign neoplasm of brain", "Benign Neoplasm of Brain", "benign neoplasm of brain", "Neoplasms, Brain, Benign", "Benign Tumor of the Brain", "Benign brain neoplasm NOS", "Brain neoplasm benign NOS", "benign tumor of the brain", "benign neoplasm of the brain", "Benign Neoplasm of the Brain", "Benign neoplasm of brain, NOS", "Benign neoplasm of brain (disorder)", "Benign neoplasm of brain unspecified", "benign neoplasm of brain (diagnosis)", "Benign neoplasm of brain, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of brain", "shortest_name_length": 18}
{"curie": "MONDO:0000610", "names": ["Marantic endocarditis", "marantic endocarditis", "Marantic Endocarditis", "Endocarditis, Marantic", "Marantic Endocarditides", "Endocarditides, Marantic", "Non-Infective Endocarditis", "Non Infective Endocarditis", "Endocarditis, Non-Infective", "Endocarditis, Non Infective", "Non-Infective Endocarditides", "Endocarditides, Non-Infective", "marantic endocarditis (diagnosis)", "Nonbacterial thrombotic endocarditis", "nonbacterial thrombotic endocarditis", "Non-bacterial thrombotic endocarditis", "Non-Bacterial Thrombotic Endocarditis", "non-bacterial thrombotic endocarditis", "Endocarditis, Non-Bacterial Thrombotic", "Nonbacterial thrombotic endocarditis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "marantic endocarditis", "shortest_name_length": 21}
{"curie": "MONDO:0008159", "names": ["type i osteoporosis", "Type 1 osteoporosis", "Type I osteoporosis", "osteoporosis menopausal", "Menopausal osteoporosis", "Postmenopausal Bone Loss", "bone loss postmenopausal", "Perimenopausal Bone Loss", "postmenopausal bone loss", "Bone Loss, Perimenopausal", "Bone Loss, Postmenopausal", "Perimenopausal Bone Losses", "Postmenopausal Bone Losses", "osteoporosis postmenopausal", "POSTMENOPAUSAL OSTEOPOROSIS", "postmenopausal osteoporosis", "Postmenopausal Osteoporosis", "Osteoporosis postmenopausal", "Postmenopausal osteoporosis", "Postmenopausal Osteoporoses", "Bone Losses, Postmenopausal", "Bone Losses, Perimenopausal", "osteoporosis; postmenopausal", "Osteoporoses, Postmenopausal", "Post-Menopausal Osteoporoses", "osteoporosis, postmenopausal", "Osteoporosis, Postmenopausal", "menopausal osteoporosis post", "Post-Menopausal Osteoporosis", "OSTEOPOROSIS, POSTMENOPAUSAL", "postmenopausal; osteoporosis", "osteoporosis post menopausal", "post menopausal osteoporosis", "Osteoporosis, Post-Menopausal", "Osteoporoses, Post-Menopausal", "Osteoporosis, Post Menopausal", "Menopausal osteoporosis (disorder)", "Menopausal osteoporosis (diagnosis)", "Postmenopausal osteoporosis (disorder)", "postmenopausal osteoporosis (diagnosis)", "bone mineral density quantitative trait locus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postmenopausal osteoporosis", "shortest_name_length": 19}
{"curie": "MONDO:0003990", "names": ["breast myoepithelial carcinoma", "Breast Myoepithelial Carcinoma", "breast malignant myoepithelioma", "Breast Malignant Myoepithelioma", "Malignant Breast Myoepithelioma", "malignant breast myoepithelioma", "malignant myoepithelioma of breast", "malignant myoepithelioma of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant breast myoepithelioma", "shortest_name_length": 30}
{"curie": "MONDO:0008655", "names": ["vestibulocochlear dysfunction, progressive", "VESTIBULOCOCHLEAR DYSFUNCTION, PROGRESSIVE", "Vestibulocochlear Dysfunction, Progressive", "Familial progressive vestibulocochlear dysfunction", "familial progressive vestibulocochlear dysfunction", "Vestibulocochlear dysfunction progressive familial", "Familial progressive vestibulo-cochlear dysfunction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vestibulocochlear dysfunction, progressive", "shortest_name_length": 42}
{"curie": "UMLS:C2981697", "names": ["Stage IC Eyelid Carcinoma", "Stage IC Eyelid Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IC Eyelid Carcinoma AJCC v7", "shortest_name_length": 25}
{"curie": "MONDO:0011173", "names": ["THCYT2", "thrombocythemia 2", "THROMBOCYTHEMIA 2", "thrombocythemia type 2", "MPL familial thrombocytosis", "familial thrombocytosis caused by mutation in MPL", "thrombocythemia 2, autosomal dominant, somatic mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombocythemia 2", "shortest_name_length": 6}
{"curie": "UMLS:C0221409", "names": ["JAUNDICE ACHOLURIC", "Jaundice acholuric", "acholuric; icterus", "Acholuric jaundice", "JAUNDICE, ACHOLURIC", "acholuric; jaundice", "jaundice; acholuric", "Chronic acholuric jaundice", "Minkowski-Chauffard disease", "Congenital hemolytic jaundice", "hemolytic; icterus, congenital", "icterus; hemolytic, congenital", "JAUNDICE, HEMOLYTIC, CONGENITAL", "jaundice; hemolytic, congenital", "hemolytic; jaundice, congenital", "Debrie's familial haemolytic disease", "Minkowski-Chauffard-Gänsslen syndrome", "Minkowski-Chauffard haemolytic jaundice", "Anemia, hereditary spherocytic hemolytic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anemia, hereditary spherocytic hemolytic", "shortest_name_length": 18}
{"curie": "MONDO:0005623", "names": ["Autoimmune Thyroiditis", "Autoimmune thyroiditis", "THYROIDITIS AUTOIMMUNE", "autoimmune thyroiditis", "thyroiditis autoimmune", "THYROIDITIS, AUTOIMMUNE", "Lymphocytic thyroiditis", "lymphocytic thyroiditis", "autoimmune; thyroiditis", "Thyroiditis, Autoimmune", "Lymphocytic Thyroiditis", "thyroiditis; autoimmune", "Lymphomatous Thyroiditis", "lymphomatous thyroiditis", "Thyroiditis, Lymphocytic", "autoimmune thyroiditides", "thyroiditis, lymphocytic", "Autoimmune Thyroiditides", "Thyroiditis, Lymphomatous", "Thyroiditides, Autoimmune", "thyroiditis, lymphomatous", "Lymphocytic Thyroiditides", "lymphocytic thyroiditides", "thyroiditides, autoimmune", "Thyroiditides, Lymphocytic", "autoimmune thyroid disease", "lymphomatous thyroiditides", "Lymphomatous Thyroiditides", "thyroiditides, lymphocytic", "Thyroiditides, Lymphomatous", "Autoimmune thyroiditis, NOS", "thyroiditides, lymphomatous", "Autoimmune thyroiditis (disorder)", "Lymphocytic thyroiditis (disorder)", "autoimmune thyroiditis (diagnosis)", "autoimmune thyroid gland inflammation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune thyroid disease", "shortest_name_length": 22}
{"curie": "MONDO:0007198", "names": ["Ascher syndrome", "ASCHER SYNDROME", "Ascher Syndrome", "Ascher's syndrome", "Ascher's syndrome (disorder)", "blepharochalasis - double lip", "BLEPHAROCHALASIS AND DOUBLE LIP", "blepharochalasis and Double lip", "blepharochalasis and double lip", "blepharochalasis and DOUBLE LIP", "Blepharochalasis And Double Lip", "Blepharochalasis and double lip", "blepharochalasis-double lip syndrome", "blepharochalasis and Double type lip", "Blepharochalasis-double lip syndrome", "Blepharochalasis, struma, double lip syndrome", "Double upper lip, blepharochalasis and enlargement of the thyroid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ascher syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0010686", "names": ["NSX", "N syndrome", "N SYNDROME", "N syndrome (disorder)", "mental retardation, malformations, chromosome breakage, and development of T-cell leukemia", "intellectual disability, malformations, chromosome breakage, and development of T-cell leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "N syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0021518", "names": ["Benign Hard Palate Tumor", "benign hard palate tumor", "benign hard palate neoplasm", "Benign tumor of hard palate", "Benign Hard Palate Neoplasm", "hard palate benign neoplasm", "Benign Tumor of Hard Palate", "benign tumor of hard palate", "Benign tumour of hard palate", "benign neoplasm of hard palate", "Benign neoplasm of hard palate", "Benign Neoplasm of Hard Palate", "benign tumor of the hard palate", "Benign Tumor of the Hard Palate", "Benign Neoplasm of the Hard Palate", "benign neoplasm of the hard palate", "Benign neoplasm of the hard palate", "Benign neoplasm of hard palate (disorder)", "benign neoplasm of hard palate (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of hard palate", "shortest_name_length": 24}
{"curie": "UMLS:C0236807", "names": ["Amphetamine Abuse", "Amphetamine abuse", "abuse amphetamine", "amphetamine abuse", "amfetamine; abuse", "abuse amphetamines", "Abuse, Amphetamine", "DRUG ABUSE AMPHETAMINE", "Drug abuse using speed", "abuse amphetamines drug", "Abuse;drug(s);amphetamine", "amphetamine abuse (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Amphetamine Abuse", "shortest_name_length": 17}
{"curie": "UMLS:C4727417", "names": ["Recurrent Submandibular Gland Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Submandibular Gland Squamous Cell Carcinoma", "shortest_name_length": 53}
{"curie": "UMLS:C5237757", "names": ["Localized Anaplastic Large Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized Anaplastic Large Cell Lymphoma", "shortest_name_length": 40}
{"curie": "UMLS:C0877322", "names": ["muscle tightness", "Muscle tightness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Muscle tightness", "shortest_name_length": 16}
{"curie": "MONDO:0020582", "names": ["benign uterine ligament neoplasm", "Benign Uterine Ligament Neoplasm", "Benign neoplasm of uterine ligament"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign uterine ligament neoplasm", "shortest_name_length": 32}
{"curie": "UMLS:C4684772", "names": ["Serious ADR", "serious adverse drug reaction", "Serious Adverse Drug Reaction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Serious Adverse Drug Reaction", "shortest_name_length": 11}
{"curie": "UMLS:C5418574", "names": ["Locally Advanced Malignant Head and Neck Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Malignant Head and Neck Neoplasm", "shortest_name_length": 49}
{"curie": "MONDO:0005453", "names": ["Heart Defect", "Heart defect", "heart defect", "heart anomaly", "Anomaly heart", "ANOMALY HEART", "anomaly heart", "Heart defects", "Heart Defects", "anomaly; heart", "heart; anomaly", "Cardiac anomaly", "CARDIAC ANOMALY", "cardiac anomaly", "ANOMALY CARDIAC", "anomalies heart", "anomaly; cardiac", "deformity; heart", "cardiac; anomaly", "heart; deformity", "heart abnormality", "anomalies cardiac", "Heart Abnormality", "Cardiac anomalies", "Abnormality, heart", "heart malformation", "HEART MALFORMATION", "Abnormality, Heart", "Heart malformation", "Heart Malformation", "heart malformations", "cardiac abnormality", "heart abnormalities", "abnormalities heart", "CARDIAC ABNORMALITY", "Cardiac abnormality", "Heart Abnormalities", "abnormality cardiac", "Heart malformations", "Heart--Abnormalities", "abnormalities, heart", "abnormalities cardiac", "Malformation Of Heart", "Cardiac abnormalities", "HEART, MALFORMATION OF", "Heart, Malformation Of", "Malformation Of Hearts", "heart, malformation Of", "Abnormally shaped heart", "congenital heart defect", "congenital defect heart", "Congenital Heart Defect", "Heart-congenital defect", "Congenital heart defect", "heart-congenital defect", "Heart disease congenital", "CONGENITAL HEART DISEASE", "heart defect, congenital", "Congenital heart defects", "Congenital heart disease", "congenital heart disease", "MALFORMATION HEART (NOS)", "Congenital Heart Defects", "congenital heart anomaly", "HEART DISEASE CONGENITAL", "Defect, Congenital Heart", "congenital defects heart", "Malformation heart (NOS)", "Abnormality of the heart", "defect, congenital heart", "congenital heart defects", "Congenital Heart Disease", "Congenital anomaly;heart", "Heart Defect, Congenital", "Defects, Congenital Heart", "Disease, Congenital Heart", "Congenital Heart Diseases", "congenital defects hearts", "congenital cardiac defect", "CARDIAC DEFECT CONGENITAL", "Heart Disease, Congenital", "Abnormal heart morphology", "congenital heart disorder", "Heart Defects, Congenital", "defects, congenital heart", "Heart Diseases, Congenital", "Congenital cardiac defects", "heart; disease, congenital", "CONGENITAL CARDIAC ANOMALY", "cardiac congenital defects", "anomaly; heart, congenital", "Congenital disease of heart", "congenital anomaly of heart", "Congenital anomaly of heart", "Congenital heart disease NOS", "Congenital cardiac anomalies", "Congenital cardiac disorders", "Congenital heart disease, NOS", "CHD - Congenital heart disease", "Disease heart congenital (NOS)", "DISEASE HEART CONGENITAL (NOS)", "congenital anomaly of the heart", "Congenital anomaly of heart NOS", "Congenital anomaly of heart, NOS", "Abnormality of cardiac morphology", "CONGENITAL ANOMALIES OF THE HEART", "congenital heart defect (diagnosis)", "Congenital heart disease (disorder)", "congenital heart disease (diagnosis)", "Unspecified congenital anomaly of heart", "disease (or disorder); heart, congenital", "Congenital malformation of heart, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital heart disease", "shortest_name_length": 12}
{"curie": "UMLS:C1504456", "names": ["Implant site rash"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Implant site rash", "shortest_name_length": 17}
{"curie": "UMLS:C0751594", "names": ["zellweger-like syndrome", "Zellweger-Like Syndrome", "Zellweger Like Syndrome", "Zellweger like syndrome", "Zellweger-like syndrome", "Zellweger's-like syndrome", "zellweger-like syndrome (diagnosis)", "Zellweger's-like syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Zellweger-Like Syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0011672", "names": ["PPBL", "Persistent polyclonal B-cell lymphocytosis", "Persistent Polyclonal B-Cell Lymphocytosis", "PERSISTENT POLYCLONAL B-CELL LYMPHOCYTOSIS", "lymphocytosis persistent polyclonal b-cell", "persistent polyclonal B-cell lymphocytosis", "PPBL - persistent polyclonal B-cell lymphocytosis", "Persistent polyclonal B-cell lymphocytosis (disorder)", "Persistent polyclonal B-cell lymphocytosis (diagnosis)", "Persistent polyclonal B-cell lymphocytosis with binucleated lymphocytes", "persistent polyclonal B-cell lymphocytosis with binucleated lymphocytes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "persistent polyclonal B-cell lymphocytosis", "shortest_name_length": 4}
{"curie": "MONDO:0020863", "names": ["diphtheria; larynx", "Laryngeal Diphtheria", "laryngeal diphtheria", "larynx; diphtheritic", "Laryngeal diphtheria", "Diphtheria, laryngeal", "diphtheria; laryngotracheitis", "Diphtheritic laryngotracheitis", "diphtheritic laryngotracheitis", "laryngotracheitis; diphtheritic", "Laryngeal diphtheria (disorder)", "diphtheritic; laryngotracheitis", "laryngeal diphtheria (diagnosis)", "diphtheritic laryngotracheitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laryngeal diphtheria", "shortest_name_length": 18}
{"curie": "UMLS:C1377919", "names": ["Stage IV Nasopharynx Carcinoma", "Metastatic Nasopharynx Carcinoma", "Stage IV Nasopharyngeal Carcinoma", "Stage IV Carcinoma of Nasopharynx", "Metastatic Nasopharyngeal Carcinoma", "Metastatic Carcinoma of Nasopharynx", "Stage IV Carcinoma of the Nasopharynx", "Metastatic Carcinoma of the Nasopharynx"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Nasopharyngeal Carcinoma", "shortest_name_length": 30}
{"curie": "UMLS:C1333424", "names": ["Epithelioid Sarcoma NCI Grade 2", "Epithelioid Sarcoma NCI Grade II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epithelioid Sarcoma NCI Grade 2", "shortest_name_length": 31}
{"curie": "UMLS:C3839106", "names": ["Carney Bone Tumor", "Osteochondromyxoma", "Osteochondromyxoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Osteochondromyxoma", "shortest_name_length": 17}
{"curie": "MONDO:0016485", "names": ["USH3", "USH3A", "Usher Syndrome Type 3", "Usher syndrome type 3", "Usher Syndrome, Type 3", "USHER SYNDROME, TYPE III", "Usher Syndrome, Type III", "USHER SYNDROME, TYPE IIIA", "Usher syndrome type 3 (diagnosis)", "Retinitis pigmentosa-deafness syndrome type 3", "Retinitis pigmentosa-deafness syndrome type 3 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Usher syndrome type 3", "shortest_name_length": 4}
{"curie": "UMLS:C0854416", "names": ["pulmonary vascular disorder", "Pulmonary vascular disorder", "Pulmonary Vascular Disorder", "Pulmonary vascular disorders", "Pulmonary vascular disorder NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pulmonary vascular disorder", "shortest_name_length": 27}
{"curie": "UMLS:C3272480", "names": ["Ampulla of Vater NEC", "Ampulla of Vater NEC G3", "Ampulla of Vater Neuroendocrine Carcinoma", "Neuroendocrine Carcinoma of the Ampullary Region", "Ampulla of Vater High Grade Neuroendocrine Carcinoma", "Ampulla of Vater Small and Large Cell Endocrine Carcinoma", "Ampulla of Vater Poorly Differentiated Endocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ampulla of Vater Neuroendocrine Carcinoma", "shortest_name_length": 20}
{"curie": "MONDO:0004562", "names": ["Breast Apocrine Carcinoma In Situ", "apocrine breast carcinoma in situ", "Apocrine Breast Carcinoma In Situ", "breast apocrine carcinoma in situ", "apocrine carcinoma in situ of breast", "Apocrine Carcinoma In Situ of Breast", "Apocrine Carcinoma In Situ of the Breast", "Apocrine carcinoma in situ of the breast", "apocrine carcinoma in situ of the breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast apocrine carcinoma in situ", "shortest_name_length": 33}
{"curie": "UMLS:C0220615", "names": ["Adult AML", "Adult AGL", "adult AML", "aml adult", "AML, adult", "adults aml", "adult ANLL", "Adult ANLL", "ANLL, adult", "Adult Acute Myeloid Leukemia", "adult acute myeloid leukemia", "Acute Myeloid Leukemia (AML)", "adult leukemia, acute myeloid", "leukemia, adult acute myeloid", "myeloid leukemia, adult acute", "acute myeloid leukemia, adult", "Adult Acute Myelocytic Leukemia", "adult acute myelogenous leukemia", "Adult Acute Myelogenous Leukemia", "acute myelogenous leukemia, adult", "Adult Acute Granulocytic Leukemia", "adult leukemia, acute myelogenous", "leukemia, adult acute myelogenous", "Adult Acute Myeloblastic Leukemia", "myelogenous leukemia, adult acute", "adult acute nonlymphocytic leukemia", "nonlymphocytic leukemia, adult acute", "Leukemia, acute myeloid (AML), adult", "adult acute non-lymphocytic leukemia", "adult leukemia, acute nonlymphocytic", "leukemia, adult acute nonlymphocytic", "acute nonlymphocytic leukemia, adult", "acute non-lymphocytic leukemia, adult", "leukemia, adult acute non-lymphocytic", "Adult Acute NonLymphoblastic Leukemia", "adult acute nonlymphoblastic leukemia", "non-lymphocytic leukemia, adult acute", "adult leukemia, acute non-lymphocytic", "nonlymphoblastic leukemia, adult acute", "adult acute non-lymphoblastic leukemia", "leukemia, adult acute nonlymphoblastic", "Adult Acute Non-Lymphoblastic Leukemia", "adult leukemia, acute nonlymphoblastic", "acute nonlymphoblastic leukemia, adult", "non-lymphoblastic leukemia, adult acute", "adult leukemia, acute non-lymphoblastic", "acute non-lymphoblastic leukemia, adult", "leukemia, adult acute non-lymphoblastic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Acute Myeloblastic Leukemia", "shortest_name_length": 9}
{"curie": "MONDO:0100189", "names": ["ApoA-I deficiency", "familial apoA-I deficiency", "apolipoprotein A-I deficiency", "familial hypoalphalipoproteinemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "apolipoprotein A-I deficiency", "shortest_name_length": 17}
{"curie": "NCIT:C171519", "names": ["Pandemic", "pandemic", "Pandemic Disease", "Pandemic Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pandemic Disorder", "shortest_name_length": 8}
{"curie": "MONDO:0030293", "names": ["HAE5", "angioedema, hereditary, 5", "ANGIOEDEMA, HEREDITARY, 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angioedema, hereditary, 5", "shortest_name_length": 4}
{"curie": "MONDO:0001997", "names": ["resorption root", "Root Resorption", "Root resorption", "root resorption", "Resorption, Root", "Root Resorptions", "Resorptions, Root"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "root resorption", "shortest_name_length": 15}
{"curie": "MONDO:0002660", "names": ["blepharochalasis", "Blepharochalasis", "Fuchs' syndrome II", "Fuchs' syndrome (2)", "Saggy upper eyelid skin", "Dermatolysis palpebrarum", "dermatolysis; palpebrarum", "palpebrarum; dermatolysis", "blepharochalasis (disease)", "Blepharochalasis (disorder)", "blepharochalasis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blepharochalasis", "shortest_name_length": 16}
{"curie": "MONDO:0100434", "names": ["Monge's disease", "chronic mountain sickness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic mountain sickness", "shortest_name_length": 15}
{"curie": "MONDO:0000707", "names": ["Disuse colitis", "Diversion colitis", "diversion colitis", "Diversion colitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diversion colitis", "shortest_name_length": 14}
{"curie": "MONDO:0016193", "names": ["qualitative or quantitative defects of alpha-actin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of alpha-actin", "shortest_name_length": 50}
{"curie": "MONDO:0032687", "names": ["IDDBAS", "IDDABS", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH ABNORMAL BEHAVIOR, MICROCEPHALY, AND SHORT STATURE", "intellectual developmental disorder with abnormal behavior, microcephaly, and short stature"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder with abnormal behavior, microcephaly, and short stature", "shortest_name_length": 6}
{"curie": "MONDO:0004112", "names": ["radiation cystitis", "Cystitis radiation", "cystitis radiation", "Radiation Cystitis", "Radiation cystitis", "irradiation cystitis", "Irradiation cystitis", "irradiation; cystitis", "CYSTITIS, IRRADIATION", "cystitis; irradiation", "radiation cystitis (diagnosis)", "Irradiation cystitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radiation cystitis", "shortest_name_length": 18}
{"curie": "MONDO:0009955", "names": ["Rapadilino syndrome", "RAPADILINO syndrome", "rapadilino syndrome", "RAPADILINO SYNDROME", "Radial and patellar aplasia", "radial and patellar aplasia", "RAPADILINO syndrome (disorder)", "radial and patellar hypoplasia", "Radial and patellar hypoplasia", "absent thumbs, dislocated joints, long face with narrow palpebral fissures, long slender nose, arched palate", "RAPADILINO - radial ray malformations, patella and palate abnormalities, diarrhea and dislocated joints, limb abnormalities and little size, slender nose and normal intelligence", "RAPADILINO - radial ray malformations, patella and palate abnormalities, diarrhoea and dislocated joints, limb abnormalities and little size, slender nose and normal intelligence"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rapadilino syndrome", "shortest_name_length": 19}
{"curie": "MONDO:0003739", "names": ["selective Immunoglobulin isotype deficiency", "Selective Immunoglobulin Isotype Deficiency", "selective immunoglobulin deficiency disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "selective immunoglobulin deficiency disease", "shortest_name_length": 43}
{"curie": "UMLS:C0242183", "names": ["Hemolytic jaundice", "Hemolytic Jaundice", "jaundice hemolytic", "hemolytic jaundice", "icterus; hemolytic", "hemolytic; icterus", "Jaundice hemolytic", "JAUNDICE HEMOLYTIC", "jaundice; hemolytic", "haemolytic jaundice", "hemolytic; jaundice", "Jaundice haemolytic", "Jaundice, Hemolytic", "Jaundice;haemolytic", "Hemolytic Jaundices", "Jaundice, hemolytic", "Haemolytic jaundice", "Jaundices, Hemolytic", "Hemolytic jaundice (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jaundice, Hemolytic", "shortest_name_length": 18}
{"curie": "MONDO:0005560", "names": ["brain disease", "Brain Disease", "Brain Disorder", "brain diseases", "brain; disease", "brain disorder", "ENCEPHALOPATHY", "Brain Diseases", "brain syndrome", "encephalopathy", "Encephalopathy", "brain condition", "Brain--Diseases", "brain syndromes", "brain disorders", "Brain Disorders", "brain conditions", "disease of brain", "encephalopathies", "Encephalopathies", "Disorder of brain", "brains conditions", "disorder of brain", "Encephalopathy NOS", "encephalopathy nos", "Encephalon Disease", "Brain disorder NOS", "Encephalopathy, NOS", "conditions of brain", "Encephalon Diseases", "BRAIN DISORDER (NOS)", "Disease of brain, NOS", "brain disease or disorder", "unspecified brain disease", "Intracranial CNS Disorder", "Intracranial CNS Disorders", "CNS Disorder, Intracranial", "encephalopathy (diagnosis)", "encephalopathy unspecified", "Encephalopathy, unspecified", "CNS Disorders, Intracranial", "disease or disorder of brain", "disease (or disorder); brain", "Disorder of brain (disorder)", "disorder of brain (diagnosis)", "Disorder of brain, unspecified", "Unspecified condition of brain", "brain conditions (non-specific)", "conditions of brain (diagnosis)", "Encephalopathy, not elsewhere classified", "Intracranial Central Nervous System Disorders", "Central Nervous System Intracranial Disorders", "Central Nervous System Disorders, Intracranial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brain disorder", "shortest_name_length": 13}
{"curie": "MONDO:0009072", "names": ["DWM", "DWS", "DW complex", "Dandy-Walker", "Dandy-Walker Cyst", "cyst dandy walker", "Dandy-Walker cyst", "dandy-walker cyst", "cyst; Dandy-Walker", "Cyst, Dandy-Walker", "Dandy-Walker Cysts", "cyst dandy walkers", "Dandy-Walker; cyst", "Cysts, Dandy-Walker", "Dandy-Walker Complex", "Dandy-walker anomaly", "Dandy-Walker anomaly", "Dandy-Walker complex", "Dandy Walker Complex", "DANDY-WALKER SYNDROME", "dandy syndrome walker", "DANDY WALKER SYNDROME", "walker dandy syndrome", "dandy-walker syndrome", "Dandy Walker Syndrome", "syndrome dandy walker", "Dandy-Walker syndrome", "dandy walker syndrome", "Dandy-Walker Syndrome", "dandy syndrome walkers", "Dandy-Walker Deformity", "Dandy Walker Deformity", "dandy walkers syndrome", "Dandy-Walker deformity", "Dandy-Walker Complices", "dandies syndrome walker", "Dandy-Walker Deformities", "Dandy Walker malformation", "DANDY-WALKER MALFORMATION", "dandy-walker malformation", "Dandy-Walker Malformation", "Dandy Walker Malformation", "dandy malformation walker", "Dandy-Walker malformation", "dandy walker malformation", "dandy malformations walker", "Malformation, Dandy-Walker", "Dandy-Walker syndrome (DWS)", "noncommunicating hydrocephalus", "Dandy-Walker malformation (DWM)", "Dandy-Walker syndrome (disorder)", "Luschka-Magendie Foramina Atresia", "Dandy-Walker syndrome (diagnosis)", "Luschka Magendie Foramina Atresia", "isolated Dandy-Walker malformation", "Dandy-Walker syndrome, Isolated cases", "mega cisterna magna (type of DW complex)", "Dandy-Walker variant (type of DW complex)", "Hydrocephalus, Internal, Dandy-Walker Type", "Atresia of foramina of Magendie and Luschka", "atresia of foramina of Magendie and Luschka", "atresia of the foramen of Luschka and Magendie", "Hydrocephalus, Noncommunicating, Dandy-Walker Type", "Dandy-Walker syndrome or malformation (type of DW complex)", "Hydrocephalus with atresia of foramina of Magendie and Luschka"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dandy-Walker syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C3273212", "names": ["HPV-Related Adenosquamous Carcinoma", "Human Papillomavirus-Related Adenosquamous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Human Papillomavirus-Related Adenosquamous Carcinoma", "shortest_name_length": 35}
{"curie": "MONDO:0009375", "names": ["fusion; hymen", "hymen; fusion", "Imperforate hymen", "Imperforate Hymen", "imperforate hymen", "hymen imperforated", "imperforate; hymen", "HYMEN, IMPERFORATE", "Hymen, Imperforate", "hymen, imperforate", "hymen; imperforate", "HYMEN IMPERFORATION", "Imperforate hymen (disorder)", "imperforate hymen (diagnosis)", "imperforate hymen (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hymen, imperforate", "shortest_name_length": 13}
{"curie": "UMLS:C1883669", "names": ["Aplastic Anemia due to Hepatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aplastic Anemia due to Hepatitis", "shortest_name_length": 32}
{"curie": "UMLS:C4331316", "names": ["Stage I Major Salivary Gland Cancer", "Stage I Major Salivary Gland Cancer AJCC v8", "Stage I Major Salivary Gland Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Major Salivary Gland Cancer AJCC v8", "shortest_name_length": 35}
{"curie": "MONDO:0008928", "names": ["Begeer syndrome", "cataract ataxia deafness", "Cataract ataxia deafness", "Cataract ataxia deafness syndrome", "cataract ataxia deafness syndrome", "cataract-ataxia-deafness syndrome", "Cataract-ataxia-deafness syndrome", "Cataract-ataxia-hearing loss syndrome", "polyneuropathy-cataract-deafness syndrome", "Polyneuropathy-Cataract-Deafness Syndrome", "POLYNEUROPATHY-CATARACT-DEAFNESS SYNDROME", "Polyneuropathy, cataract, deafness syndrome", "polyneuropathy, cataract, deafness syndrome", "CATARACT-ATAXIA-DEAFNESS-RETARDATION SYNDROME", "Cataract-ataxia-deafness-retardation syndrome", "cataract-ataxia-deafness-retardation syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract-ataxia-deafness syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0018979", "names": ["MMN", "MMNCB", "multifocal motor neuropathy", "Multifocal motor neuropathy", "multifocal motor neuropathy (diagnosis)", "Motor neuropathy with multiple conduction block", "Multifocal motor neuropathy with conduction block", "multifocal motor neuropathy with conduction block", "MMN - Motor neuropathy with multiple conduction block", "Motor neuropathy with multiple conduction block (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multifocal motor neuropathy", "shortest_name_length": 3}
{"curie": "UMLS:C4744722", "names": ["Advanced Cervical Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Cervical Carcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C0278861", "names": ["Relapsed Thyroid Cancer", "Recurrent Thyroid Cancer", "Thyroid cancer recurrent", "recurrent thyroid cancer", "thyroid cancer recurrent", "thyroid cancer, recurrent", "Relapsed Cancer of Thyroid", "Recurrent Thyroid Carcinoma", "Recurrent Cancer of Thyroid", "Relapsed Thyroid Gland Cancer", "Relapsed Cancer of the Thyroid", "Recurrent Thyroid Gland Cancer", "Recurrent Cancer of the Thyroid", "Relapsed Cancer of Thyroid Gland", "Recurrent Cancer of Thyroid Gland", "Recurrent Thyroid Gland Carcinoma", "Relapsed Cancer of the Thyroid Gland", "Recurrent Cancer of the Thyroid Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Thyroid Carcinoma", "shortest_name_length": 23}
{"curie": "UMLS:C0032568", "names": ["Pseudopolyp", "pseudopolyp", "pseudopolyps", "pseudopolyposis", "Pseudopolyposis", "Pseudopolyp, NOS", "inflammatory polyp", "Inflammatory polyp", "Polyp, inflammatory", "inflammatory polyps", "Pseudopolyposis, NOS", "Inflammatory pseudopolyp", "Pseudopolyp, inflammatory", "Inflammatory polyp (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Inflammatory polyp", "shortest_name_length": 11}
{"curie": "UMLS:C0443306", "names": ["Spastic", "spastic", "spastics", "Spastic (qualifier value)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spastic", "shortest_name_length": 7}
{"curie": "UMLS:C2747867", "names": ["Intestinal hematoma", "Intestinal haematoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal hematoma", "shortest_name_length": 19}
{"curie": "UMLS:C5237752", "names": ["Non-Recurrent Esophageal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Recurrent Esophageal Carcinoma", "shortest_name_length": 34}
{"curie": "UMLS:C4527188", "names": ["Occult Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Occult Breast Carcinoma", "shortest_name_length": 23}
{"curie": "UMLS:C2981664", "names": ["Stage IA Distal Bile Duct Cancer", "Stage IA Distal Bile Duct Cancer AJCC v7", "Stage IA Extrahepatic (Distal) Bile Duct Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Distal Bile Duct Cancer AJCC v7", "shortest_name_length": 32}
{"curie": "MONDO:0003816", "names": ["Articular cartilage disease", "articular cartilage disease", "articular cartilage disorder", "Articular cartilage disorder", "cartilage; disorder, articular", "disorder of articular cartilage", "Disorder of articular cartilage", "Articular cartilage disease, NOS", "Articular cartilage disorder, NOS", "articular cartilage disorder of hand", "articular cartilage of joint disease", "Articular cartilage disorder (disorder)", "articular cartilage disorder of forearm", "disease of articular cartilage of joint", "disorder of articular cartilage of joint", "articular cartilage disorder (diagnosis)", "articular cartilage disorder of upper arm", "articular cartilage disorder involving hand", "Articular cartilage disorder, site unspecified", "articular cartilage disorder involving forearm", "articular cartilage disorder of multiple sites", "articular cartilage disorder of shoulder region", "articular cartilage disorder involving upper arm", "articular cartilage of joint disease or disorder", "articular cartilage disorder of ankle and/or foot", "disease or disorder of articular cartilage of joint", "articular cartilage disorder involving ankle and foot", "articular cartilage disorder involving multiple sites", "articular cartilage disorder involving shoulder region", "articular cartilage disorder of the pelvic region and thigh", "articular cartilage disorder involving pelvic region and thigh"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "articular cartilage disorder", "shortest_name_length": 27}
{"curie": "MONDO:0004295", "names": ["asbestos-related lung cancer", "Asbestos-Related Lung Cancer", "asbestos-related lung carcinoma", "Asbestos-Related Lung Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "asbestos-related lung carcinoma", "shortest_name_length": 28}
{"curie": "UMLS:C0266335", "names": ["anomaly; bladder", "bladder; anomaly", "Bladder malformation", "Congenital bladder anomaly", "Congenital anomaly;bladder", "congenital anomaly of bladder", "Congenital bladder anomaly NOS", "bladder; deformity, congenital", "Congenital anomaly of the bladder", "congenital anomaly of the bladder", "CONGENITAL ANOMALIES OF THE BLADDER", "Congenital abnormality of the bladder", "Congenital malformation of the bladder", "Congenital anomaly of the bladder, NOS", "congenital anomaly of bladder (diagnosis)", "Congenital anomaly of the bladder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital anomaly of the bladder", "shortest_name_length": 16}
{"curie": "MONDO:0021517", "names": ["Benign Trachea Tumor", "benign trachea tumor", "benign tracheal tumor", "Benign Tracheal Tumor", "Benign Tumor of Trachea", "Benign tumor of trachea", "benign trachea neoplasm", "benign tumor of trachea", "Benign Trachea Neoplasm", "trachea benign neoplasm", "Benign tracheal neoplasm", "tracheal neoplasm benign", "Benign Tracheal Neoplasm", "benign tracheal neoplasm", "Benign tumour of trachea", "benign neoplasm of trachea", "Benign neoplasm of trachea", "Benign Neoplasm of Trachea", "Benign Tumor of the Trachea", "benign tumor of the trachea", "benign neoplasm of the trachea", "Benign Neoplasm of the Trachea", "Benign neoplasm of trachea, NOS", "benign tracheal neoplasm (diagnosis)", "Benign neoplasm of trachea (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of trachea", "shortest_name_length": 20}
{"curie": "UMLS:C1332898", "names": ["Centroblastic Lymphoma PTLD", "Centroblastic Diffuse Large B-Cell Lymphoma PTLD", "Centroblastic Lymphoma Post-Transplant Lymphoproliferative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Centroblastic Lymphoma Post-Transplant Lymphoproliferative Disorder", "shortest_name_length": 27}
{"curie": "MONDO:0012949", "names": ["ANIB9", "Anib9", "intracranial berry aneurysm 9", "Aneurysm, Intracranial Berry, 9", "aneurysm, intracranial BERRY, 9", "ANEURYSM, INTRACRANIAL BERRY, 9", "aneurysm, intracranial berry, 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aneurysm, intracranial berry, 9", "shortest_name_length": 5}
{"curie": "MONDO:0035410", "names": ["isolated congenital aglossia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated congenital aglossia", "shortest_name_length": 28}
{"curie": "MONDO:0016683", "names": ["gliomatosis", "Gliomatosis", "Gliomatosis Cerebri", "gliomatosis cerebri", "Gliomatosis cerebri", "gliomatosis; cerebri", "astrocytosis cerebri", "Astrocytosis cerebri", "Gliomatosis cerebri (disorder)", "Gliomatosis cerebri (morphologic abnormality)", "gliomatosis cerebri (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gliomatosis cerebri", "shortest_name_length": 11}
{"curie": "MONDO:0001199", "names": ["ossicular dislocation", "Ossicular dislocation", "dislocation of ossicles", "Dislocation of ossicles", "ossicle chain disruption", "dislocation; ear ossicles", "dislocation of ear ossicle", "Dislocation of ear ossicles", "dislocation of ear ossicles", "ossicle chain discontinuity", "ossicle chain disarticulation", "Ossicle chain disarticulation", "auditory ossicles; dislocation", "Dislocation of ear ossicles (disorder)", "dislocation of ear ossicles (diagnosis)", "Discontinuity or dislocation of ear ossicles"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dislocation of ear ossicle", "shortest_name_length": 21}
{"curie": "MONDO:0005091", "names": ["SARS", "SARS-1", "SARS-CoV infection", "SARS-CoV-1 infection", "SARS-associated coronavirus", "Severe Acute Respiratory Syndrome", "severe acute respiratory syndrome", "Severe acute respiratory syndrome", "Respiratory Syndrome, Severe Acute", "SARS coronavirus infectious disease", "Respiratory Syndrome, Acute, Severe", "SARS coronavirus disease or disorder", "Severe acute respiratory syndrome NOS", "SARS-associated coronavirus (diagnosis)", "acute respiratory coronavirus infection", "SARS (Severe Acute Respiratory Syndrome)", "severe acute respiratory syndrome (SARS)", "SARS coronavirus caused disease or disorder", "Severe acute respiratory syndrome (disorder)", "severe acute respiratory syndrome (SARS) (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe acute respiratory syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C3899651", "names": ["Childhood Nasal Cavity Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Nasal Cavity Carcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C0233800", "names": ["CONFABULATION", "confabulation", "Confabulation", "confabulations", "Confabulation (finding)", "Invents experiences to compensate for loss of memory"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Confabulation", "shortest_name_length": 13}
{"curie": "MONDO:0013266", "names": ["MRD20", "NEDHSIL", "MRD20, FORMERLY", "chromosome 5q14.3 deletion syndrome", "autosomal dominant mental retardation 20", "mental retardation, autosomal dominant 20", "autosomal dominant intellectual disability 20", "chromosome 5Q14.3 deletion syndrome, proximal", "CHROMOSOME 5q14.3 DELETION SYNDROME, PROXIMAL", "mental retardation, autosomal dominant type 20", "intellectual disability, autosomal dominant 20", "intellectual disability, autosomal dominant type 20", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 20, FORMERLY", "MEF2C autosomal dominant non-syndromic intellectual disability", "MENTAL RETARDATION, STEREOTYPIC MOVEMENTS, EPILEPSY, AND/OR CEREBRAL MALFORMATIONS", "mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations", "autosomal dominant non-syndromic intellectual disability caused by mutation in MEF2C", "intellectual disability, stereotypic movements, epilepsy, and/or cerebral malformations", "NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, STEREOTYPIC HAND MOVEMENTS, AND IMPAIRED LANGUAGE", "neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 20", "shortest_name_length": 5}
{"curie": "UMLS:C5670681", "names": ["Stage IIIB Cervical Cancer FIGO 2009", "Stage IIIB Cervical Carcinoma FIGO 2009"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Cervical Cancer FIGO 2009", "shortest_name_length": 36}
{"curie": "UMLS:C0152086", "names": ["TRAUMATIC ARTHRITIS", "Traumatic Arthritis", "traumatic arthritis", "Arthritis;traumatic", "ARTHRITIS TRAUMATIC", "Traumatic arthritis", "traumatic; arthritis", "arthritis; traumatic", "Traumatic Arthropathy", "traumatic arthropathy", "Traumatic arthropathy", "traumatic; arthropathy", "arthropathy; traumatic", "Posttraumatic arthropathy", "Arthritis secondary to trauma", "ARTHRITIS, TRAUMATIC, PRIMARY", "traumatic arthritis (diagnosis)", "Traumatic arthropathy (disorder)", "traumatic arthropathy (diagnosis)", "Traumatic arthropathy, unspecified site", "Traumatic arthropathy, site unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Traumatic arthropathy", "shortest_name_length": 19}
{"curie": "UMLS:C5670552", "names": ["Metastatic Ovarian High Grade Serous Adenocarcinoma", "Metastatic Ovarian High-Grade Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Ovarian High Grade Serous Adenocarcinoma", "shortest_name_length": 51}
{"curie": "MONDO:0002368", "names": ["PPC", "EOPPC", "papillary serous carcinoma", "Papillary serous carcinoma", "Papillary Serous Carcinoma", "Low grade serous carcinoma", "Primary peritoneal carcinoma", "Papillary Serous Adenocarcinoma", "serous papillary adenocarcinoma", "micropapillary serous carcinoma", "Papillary serous adenocarcinoma", "Micropapillary Serous Carcinoma", "Micropapillary serous carcinoma", "papillary serous adenocarcinoma", "adenocarcinomas papillary serous", "Serous Surface Papillary Carcinoma", "serous surface papillary carcinoma", "Serous surface papillary carcinoma", "papillary serous cystadenocarcinoma", "Primary peritoneal serous carcinoma", "Papillary Serous Cystadenocarcinoma", "Papillary serous cystadenocarcinoma", "Extraovarian primary peritoneal carcinoma", "Extra-ovarian primary peritoneal carcinoma", "EOPPC - Extraovarian primary peritoneal carcinoma", "Micropapillary Variant of Serous Borderline Tumor", "Low grade serous carcinoma (morphologic abnormality)", "Extraovarian primary peritoneal carcinoma (disorder)", "Extraovarian primary peritoneal carcinoma (diagnosis)", "peritoneal neoplasm malignant carcinoma extraovarian primary", "serous surface papillary carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papillary serous cystadenocarcinoma", "shortest_name_length": 3}
{"curie": "MONDO:0006258", "names": ["Juvenile Polyp", "juvenile polyp", "Juvenile polyp", "retention polyp", "juvenile polyps", "polyps juvenile", "Retention polyp", "Retention Polyp", "POLYPS, JUVENILE", "Juvenile polyp (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile polyp", "shortest_name_length": 14}
{"curie": "MONDO:0025385", "names": ["bluetongue", "Bluetongue", "tongue blue", "Blue Tongue", "blue tongue", "tongue, blue", "Tongue, Blue", "Bluetongue infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bluetongue", "shortest_name_length": 10}
{"curie": "UMLS:C1708766", "names": ["Lung NET G2", "Lung NET Grade 2", "Lung NET, Grade 2", "Lung Neuroendocrine Tumor G2", "Lung Atypical Carcinoid Tumor", "atypical carcinoid tumor of lung", "Lung Neuroendocrine Tumor Grade 2", "malignant carcinoid tumor of lung", "Malignant carcinoid tumor of lung", "Lung Neuroendocrine Tumor, Grade 2", "Malignant carcinoid tumor of lung (disorder)", "atypical carcinoid tumor of lung (diagnosis)", "malignant carcinoid tumor of lung (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant carcinoid tumor of lung", "shortest_name_length": 11}
{"curie": "UMLS:C2698310", "names": ["B lymphoblastic leukemia/lymphoma, NOS", "B Lymphoblastic Leukemia/Lymphoma, NOS", "B Lymphoblastic Leukemia/Lymphoma, Not Otherwise Specified", "B-Lymphoblastic Leukemia/Lymphoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B Lymphoblastic Leukemia/Lymphoma, Not Otherwise Specified", "shortest_name_length": 38}
{"curie": "UMLS:C1332294", "names": ["Castleman Disease, Plasma Cell Type", "Castleman's Disease, Plasma Cell Type", "Angiofollicular Lymphoid Hyperplasia, Plasma Cell Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Castleman Disease, Plasma Cell Type", "shortest_name_length": 35}
{"curie": "UMLS:C0341365", "names": ["fistula colon", "colon fistula", "colon; fistula", "colon fistulas", "fistula; colon", "colonic fistula", "Colonic Fistula", "Colonic fistula", "COLON NOS FISTULA", "Large Bowel Fistula", "Colonic fistula (disorder)", "Colonic fistula (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colonic fistula", "shortest_name_length": 13}
{"curie": "UMLS:C0267085", "names": ["Pulsion Diverticulum", "EPIPHRENIC DIVERTICULUM", "Epiphrenic diverticulum", "Epiphrenic Diverticulum", "Supradiaphragmatic diverticulum", "epiphrenic esophageal diverticula", "Acquired epiphrenic diverticulum of esophagus", "epiphrenic esophageal diverticula (diagnosis)", "Acquired epiphrenic diverticulum of oesophagus", "Acquired supradiaphragmatic diverticulum of esophagus", "Acquired supradiaphragmatic diverticulum of oesophagus", "Acquired supradiaphragmatic diverticulum of esophagus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired supradiaphragmatic diverticulum of esophagus", "shortest_name_length": 20}
{"curie": "MONDO:0009174", "names": ["CHAPLE", "CHAPLE syndrome", "CD55 deficiency", "Exudative enteropathy", "Exudative Enteropathy", "exudative enteropathy", "Enteropathy, Exudative", "Enteropathy, exudative", "enteropathy, exudative", "Exudative Enteropathies", "Enteropathies, Exudative", "enteropathy protein losing", "PROTEIN-LOSING ENTEROPATHY", "Protein-losing enteropathy", "protein losing enteropathy", "PROTEIN LOSING ENTEROPATHY", "Protein-Losing Enteropathy", "Protein Losing Enteropathy", "protein-losing enteropathy", "enteropathy; protein-losing", "Enteropathy, Protein-Losing", "enteropathy, PROTEIN-losing", "Enteropathy, protein-losing", "ENTEROPATHY, PROTEIN-LOSING", "enteropathy, protein losing", "enteropathy, protein-losing", "protein-losing; enteropathy", "Protein-losing enteropathies", "Protein Losing Enteropathies", "Protein-Losing Enteropathies", "protein losing enteropathies", "Enteropathies, Protein-Losing", "PLE - Protein-losing enteropathy", "Exudative enteropathy (disorder)", "Protein-losing enteropathy syndrome", "protein-losing enteropathy (disease)", "Protein-losing enteropathy (disorder)", "protein losing enteropathy (diagnosis)", "complement hyperactivation, ANGIOPATHIC thrombosis, and PROTEIN-losing enteropathy", "complement hyperactivation, Angiopathic thrombosis, and Protein-losing enteropathy", "COMPLEMENT HYPERACTIVATION, ANGIOPATHIC THROMBOSIS, AND PROTEIN-LOSING ENTEROPATHY", "Complement hyperactivation-angiopathic thrombosis-protein-losing enteropathy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "protein-losing enteropathy", "shortest_name_length": 6}
{"curie": "UMLS:C3899988", "names": ["Autosomal Recessive Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Autosomal Recessive Disorder", "shortest_name_length": 28}
{"curie": "MONDO:0012517", "names": ["GDSAPC", "SAPOSIN C DEFICIENCY", "PSAP Gaucher disease", "Gaucher disease, atypical", "Gaucher disease caused by mutation in PSAP", "Gaucher disease due to saposin C deficiency", "Atypical Gaucher disease due to saposin C deficiency", "atypical Gaucher disease due to saposin C deficiency", "atypical Gaucher's disease due to saposin c deficiency", "Gaucher disease, atypical, due to saposin C deficiency", "GAUCHER DISEASE, ATYPICAL, DUE TO SAPOSIN C DEFICIENCY", "Gaucher Disease, Atypical, Due To Saposin C Deficiency", "Atypical Gaucher disease due to saposin C deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gaucher disease due to saposin C deficiency", "shortest_name_length": 6}
{"curie": "MONDO:0004700", "names": ["PAROTID TUMOR", "Parotid Tumor", "Parotid tumor", "parotid tumor", "cancer parotid", "parotid tumour", "parotid cancer", "parotid tumors", "Parotid Cancer", "Parotid tumour", "PAROTID CANCER", "parotid tumours", "Cancer, Parotid", "Parotid Cancers", "Cancers, Parotid", "Tumor of Parotid", "Parotid Neoplasm", "parotid neoplasm", "Cancer of Parotid", "Neoplasm, Parotid", "cancer of parotid", "Parotid Neoplasms", "Neoplasms, Parotid", "neoplasm of parotid", "parotid gland tumor", "Parotid Gland Tumor", "Neoplasm of Parotid", "parotid tumor gland", "Tumor of the Parotid", "parotid gland tumour", "parotid gland cancer", "Parotid Gland Cancer", "gland parotid tumors", "gland parotid tumours", "Cancer of the Parotid", "cancer of the parotid", "Parotid Gland Neoplasm", "Tumor of Parotid Gland", "tumor of parotid gland", "Parotid glands--Tumors", "Neoplasm malig;parotid", "Tumor of parotid gland", "cancer of parotid gland", "Tumour of parotid gland", "Cancer of Parotid Gland", "Malignant Parotid Tumor", "Neoplasm of the Parotid", "Parotid tumor malignant", "malignant parotid tumor", "Cancer of parotid gland", "Parotid tumour malignant", "Neoplasm of Parotid Gland", "Neoplasm of parotid gland", "parotid neoplasm malignant", "malignant parotid neoplasm", "Malignant Parotid Neoplasm", "Malignant Tumor of Parotid", "Tumor of the Parotid Gland", "malignant tumor of parotid", "cancer of the parotid gland", "Cancer of the Parotid Gland", "CA - Cancer of parotid gland", "Malignant Parotid Gland Tumor", "malignant neoplasm of parotid", "malignant parotid gland tumor", "Malignant Neoplasm of Parotid", "Neoplasm of the Parotid Gland", "malignant tumor of the parotid", "Malignant Tumor of the Parotid", "Parotid Salivary Gland Neoplasm", "neoplasm of parotid (diagnosis)", "malignant tumor of parotid gland", "Malignant tumor of parotid gland", "Malignant Tumor of Parotid Gland", "Malignant Parotid Gland Neoplasm", "malignant parotid gland neoplasm", "Malignant Neoplasm of the Parotid", "malignant neoplasm of the parotid", "Malignant tumour of parotid gland", "malignant neoplasm of the Parotid", "malignant neosplasm of the parotid", "Malignant neoplasm of parotid gland", "Malignant Neoplasm of Parotid Gland", "malignant neoplasm of parotid gland", "Neoplasm of parotid gland (disorder)", "Malignant Tumor of the Parotid Gland", "malignant tumor of the parotid gland", "Malignant Neoplasm of the Parotid Gland", "malignant neoplasm of the parotid gland", "malignant neoplasm of parotid (diagnosis)", "Malignant tumor of parotid gland (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parotid gland cancer", "shortest_name_length": 13}
{"curie": "MONDO:0006815", "names": ["Jejunal cancer", "jejunum cancer", "Jejunum Cancer", "jejunal cancer", "Jejunal Cancer", "Jejunum cancer", "Cancer, Jejunal", "Jejunum Cancers", "Jejunal Cancers", "Cancers, Jejunal", "cancer of jejunum", "Cancer of Jejunum", "Jejunum cancer NOS", "Jejunal cancer NOS", "Cancer of the Jejunum", "Malignant tumor of jejunum", "malignant tumor of jejunum", "malignant jejunal neoplasm", "Malignant Jejunal Neoplasm", "malignant jejunum neoplasm", "Malignant tumour of jejunum", "malignant neoplasm of jejunum", "Malignant neoplasm of jejunum", "Malignant neoplasm of jejunum NOS", "Malignant tumor of jejunum (disorder)", "malignant neoplasm of jejunum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "jejunal cancer", "shortest_name_length": 14}
{"curie": "MONDO:0022841", "names": ["congenital hypotrichosis milia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital hypotrichosis milia", "shortest_name_length": 30}
{"curie": "UMLS:C5420168", "names": ["Pharyngeal Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pharyngeal Hodgkin Lymphoma", "shortest_name_length": 27}
{"curie": "UMLS:C0920187", "names": ["congenital neuropathy", "Congenital neuropathy", "Congenital Neuropathy", "Congenital neuropathy NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital neuropathy", "shortest_name_length": 21}
{"curie": "MONDO:0008913", "names": ["CVDD", "CVDP1", "CARDIAC VALVULAR DYSPLASIA 1", "developmental cardiac valvular defect", "Cardiac Valvular Defect, Developmental", "cardiac valvular defect, developmental", "CARDIAC valvular defect, developmental"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiac valvular defect, developmental", "shortest_name_length": 4}
{"curie": "MONDO:0012576", "names": ["PSNP3", "Supranuclear Palsy, Progressive, 3", "SUPRANUCLEAR PALSY, PROGRESSIVE, 3", "supranuclear palsy, progressive, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "supranuclear palsy, progressive, 3", "shortest_name_length": 5}
{"curie": "MONDO:0005157", "names": ["lymphoid tumor", "Lymphoid Tumor", "Lymphoid neoplasm", "Lymphocytic Tumor", "Lymphoid Neoplasm", "lymphoid neoplasm", "lymphocytic tumor", "Lymphocytic Neoplasm", "lymphocytic neoplasm", "lymphoid and plasma cell tumor", "Lymphoid and Plasmacytic Tumor", "Lymphoid and Plasma Cell Tumor", "lymphoid and plasmacytic tumor", "Lymphoid and Plasmacytic Tumour", "lymphoid and plasma cell tumour", "lymphoid and plasmacytic tumour", "Lymphoid and Plasma Cell Tumour", "Lymphoid and Plasmacytic Neoplasm", "lymphoid and plasmacytic neoplasm", "lymphocytic and plasma cell tumor", "Lymphocytic and Plasma Cell Tumor", "lymphocytic and plasma cell tumour", "Lymphocytic and Plasma Cell Tumour", "lymphocytic and plasmacytic neoplasm", "lymphocytic and plasma cell neoplasm", "Lymphocytic and Plasmacytic Neoplasm", "Lymphocytic and Plasma Cell Neoplasm", "Lymphoid neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphoid neoplasm", "shortest_name_length": 14}
{"curie": "MONDO:0019507", "names": ["Amelogenesis imperfecta", "amelogenesis imperfecta", "Amelogenesis Imperfecta", "Congenital Enamel Hypoplasia", "Congenital enamel hypoplasia", "AI - Amelogenesis imperfecta", "Amelogenesis imperfecta (disorder)", "amelogenesis imperfecta (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amelogenesis imperfecta", "shortest_name_length": 23}
{"curie": "MONDO:0021398", "names": ["rectum polyp", "polyp rectal", "RECTUM POLYP", "rectal polyp", "Rectal Polyp", "Rectal polyp", "RECTAL POLYP", "rectum; polyp", "polyps rectum", "Rectal polyps", "polyp; rectum", "RECTUM, POLYP", "polyps rectal", "rectal polyps", "Polyp(s);rectal", "Polyp of Rectum", "Polyp of rectum", "polyp of rectum", "Rectal polyposis", "polyp of the rectum", "Polyp of the Rectum", "Multiple rectal polyps", "Rectal polyp (disorder)", "rectal polyps (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyp of rectum", "shortest_name_length": 12}
{"curie": "UMLS:C3900094", "names": ["Adult Salivary Gland Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Salivary Gland Carcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0002246", "names": ["ear; perichondritis", "perichondritis; ear", "perichondritis pinna", "pinna; perichondritis", "perichondritis; pinna", "Perichondritis of pinna", "perichondritis of pinna", "Auricular perichondritis", "perichondritis of auricle", "Perichondritis of auricle", "perichondritis; auricle, ear", "Perichondritis of pinna, NOS", "auricle, ear; perichondritis", "Perichondritis of auricle, NOS", "Perichondritis of external ear", "perichondritis of auricle of ear", "Perichondritis of pinna (disorder)", "Perichondritis of pinna, unspecified", "perichondritis of pinna, unspecified", "perichondritis of auricle (diagnosis)", "Perichondritis and chondritis of pinna", "perichondritis and chondritis of pinna", "Perichondritis of external ear (disorder)", "Unspecified perichondritis of external ear", "perichondritis of auricle of ear (physical finding)", "Unspecified perichondritis of external ear, unspecified ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "perichondritis of auricle", "shortest_name_length": 19}
{"curie": "MONDO:0019696", "names": ["St Helena dysplasia", "St. Helena Dysplasia", "Acromesomelic dwarfism", "Acromesomelic Dwarfism", "acromesomelic dwarfism", "acromesomelic dysplasia", "Acromesomelic dysplasia", "Acromesomelic dysplasia group", "Acromesomelic dysplasia syndrome", "Acromesomelic dysplasia group (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acromesomelic dysplasia", "shortest_name_length": 19}
{"curie": "UMLS:C1328402", "names": ["Metastatic glioma", "Metastatic Glioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic glioma", "shortest_name_length": 17}
{"curie": "UMLS:C1332541", "names": ["Benign Thalamic Tumor", "Benign Thalamus Tumor", "Benign Thalamic Tumors", "Benign Thalamus Tumors", "Benign Tumor of Thalamus", "Benign Thalamus Neoplasm", "Benign Thalamic Neoplasm", "Benign Thalamus Neoplasms", "Benign Thalamic Neoplasms", "Benign Neoplasm of Thalamus", "Benign Tumor of the Thalamus", "Benign Neoplasm of the Thalamus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Thalamic Neoplasm", "shortest_name_length": 21}
{"curie": "MONDO:0007137", "names": ["ANIC", "congenital anosmia", "Congenital anosmia", "Anosmia, Congenital", "ANOSMIA, CONGENITAL", "anosmia, congenital", "isolated congenital anosmia", "Isolated congenital anosmia", "anosmia, isolated congenital", "ANOSMIA, ISOLATED CONGENITAL", "Anosmia, Isolated Congenital", "Congenital anosmia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated congenital anosmia", "shortest_name_length": 4}
{"curie": "UMLS:C5237070", "names": ["Advanced Merkel Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Merkel Cell Carcinoma", "shortest_name_length": 30}
{"curie": "UMLS:C0280188", "names": ["Recurrent Diffuse Large Cell Lymphoma", "Relapsed Adult Diffuse Large Cell Lymphoma", "relapsed adult diffuse large cell lymphoma", "recurrent adult diffuse large cell lymphoma", "Recurrent Adult Diffuse Large Cell Lymphoma", "adult diffuse large cell lymphoma, relapsed", "adult diffuse large cell lymphoma, recurrent", "diffuse large cell lymphoma, recurrent, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Adult Diffuse Large Cell Lymphoma", "shortest_name_length": 37}
{"curie": "UMLS:C5667135", "names": ["Other Iatrogenic Immunodeficiency-Related Lymphoproliferative Disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Other Iatrogenic Immunodeficiency-Related Lymphoproliferative Disorders", "shortest_name_length": 71}
{"curie": "MONDO:0003996", "names": ["Basal Ganglia Disease", "basal ganglia disease", "Basal ganglia disease", "basal ganglia disorder", "Basal Ganglia Disorder", "basal disorder ganglia", "Basal Ganglia Diseases", "basal ganglia diseases", "Basal ganglia--Diseases", "basal ganglia disorders", "Basal Ganglia Disorders", "disease of basal ganglia", "disorder of basal ganglia", "Disorder of basal ganglia", "Basal ganglia abnormalities", "Anomaly of the basal ganglia", "Disease of basal ganglia, NOS", "Abnormality of the basal ganglia", "Abnormal basal ganglia morphology", "Abnormalities of the basal ganglia", "collection of basal ganglia disease", "Disorder of basal ganglia (disorder)", "disease (or disorder); basal ganglia", "disorder of basal ganglia (diagnosis)", "disease of collection of basal ganglia", "disorder of collection of basal ganglia", "collection of basal ganglia disease or disorder", "disease or disorder of collection of basal ganglia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "basal ganglia disorder", "shortest_name_length": 21}
{"curie": "MONDO:0024912", "names": ["Cat Disease", "disease cat", "cat disease", "Cat Diseases", "Disease, Cat", "disease, Cat", "cats disease", "cat diseases", "Diseases, Cat", "diseases, Cat", "cats diseases", "Feline Disease", "feline disease", "Feline disease", "Cats--Diseases", "disease felines", "Disease, Feline", "disease, Feline", "Feline diseases", "Feline Diseases", "feline diseases", "Diseases, Feline", "diseases, Feline"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cat disease", "shortest_name_length": 11}
{"curie": "UMLS:C2718304", "names": ["I2S Deficiency", "Deficiency, I2S", "Iduronate Sulfatase Deficiency", "Deficiency, Iduronate Sulfatase", "Iduronate 2 Sulfatase Deficiency", "Iduronate 2-Sulfatase Deficiency", "Deficiency, Iduronate 2-Sulfatase", "Sulfoiduronate Sulfatase Deficiency", "Deficiency, Sulfoiduronate Sulfatase"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sulfoiduronate Sulfatase Deficiency", "shortest_name_length": 14}
{"curie": "MONDO:0700150", "names": ["canine mastocytoma", "Canine Mastocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canine mastocytoma", "shortest_name_length": 18}
{"curie": "UMLS:C0345259", "names": ["Ladd Band", "bands ladd", "bands ladds", "Ladd's Band", "ladd's bands", "Ladd's bands", "Band of Ladd", "Band of Ladd (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Band of Ladd", "shortest_name_length": 9}
{"curie": "MONDO:0019479", "names": ["histiocytic sarcoma", "Histiocytic sarcoma", "Histiocytic Sarcoma", "histiocytic lymphoma", "Sarcoma, Histiocytic", "Histiocytic Sarcomas", "Sarcomas, Histiocytic", "True histiocytic lymphoma", "True Histiocytic Lymphoma", "True Histiocytic Lymphomas", "true histiocytic; lymphoma", "Lymphoma, True Histiocytic", "Histiocytic Lymphoma, True", "lymphoma; true histiocytic", "Lymphomas, True Histiocytic", "histiocytic; lymphoma, true", "Histiocytic Lymphomas, True", "lymphoma; histiocytic, true", "True Malignant Histiocytoses", "True Malignant Histiocytosis", "Malignant Histiocytoses, True", "Histiocytosis, True Malignant", "Histiocytoses, True Malignant", "Malignant Histiocytosis, True", "Histiocytic sarcoma (clinical)", "Histiocytic sarcoma (disorder)", "sarcoma, histiocytic, malignant", "histiocytic sarcoma (diagnosis)", "SARCOMA, HISTIOCYTIC, MALIGNANT", "True histiocytic lymphoma (clinical)", "Histiocytic sarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "histiocytic sarcoma", "shortest_name_length": 19}
{"curie": "UMLS:C2936847", "names": ["Acatalasemia Japanese type", "Acatalasemia Japanese Type", "Japanese Type, Acatalasemia", "ACATALASEMIA, JAPANESE TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acatalasemia Japanese type", "shortest_name_length": 26}
{"curie": "DOID:0080624", "names": ["HMLR2", "PBD4C", "HEIMLER SYNDROME 2", "Heimler syndrome 2", "PEROXISOME BIOGENESIS DISORDER 4C", "peroxisomal biogenesis disorder 4C"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Heimler syndrome 2", "shortest_name_length": 5}
{"curie": "UMLS:C0003546", "names": ["Acquired Aphasia", "acquired aphasia", "acquired; aphasia", "acquired aphasias", "Aphasia, Acquired", "aphasia; acquired"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aphasia, Acquired", "shortest_name_length": 16}
{"curie": "MONDO:0014160", "names": ["IMD7", "immunodeficiency 7", "IMMUNODEFICIENCY 7", "TCR-ALPHA/BETA DEFICIENCY", "TCR-Alpha/Beta deficiency", "TCR-alpha-beta+ T-cell deficiency", "T-CELL RECEPTOR-ALPHA/BETA DEFICIENCY", "T-cell receptor-ALPHA/BETA deficiency", "TCR-alpha-beta-positive T-cell deficiency", "immunodeficiency 7, TCR-alpha/beta deficient"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "TCR-alpha-beta-positive T-cell deficiency", "shortest_name_length": 4}
{"curie": "UMLS:C4527059", "names": ["Clinical Stage II Merkel Cell Carcinoma AJCC v8", "Clinical Stage II Neuroendocrine Carcinoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage II Merkel Cell Carcinoma AJCC v8", "shortest_name_length": 47}
{"curie": "UMLS:C4331228", "names": ["Recurrent Germ Cell Tumor", "Recurrent Germ Cell Neoplasm", "Recurrent Malignant Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Malignant Germ Cell Tumor", "shortest_name_length": 25}
{"curie": "MONDO:0006043", "names": ["MpBC", "metaplastic breast cancer", "Breast Metaplastic Carcinoma", "Metaplastic breast carcinoma", "metaplastic breast carcinoma", "breast metaplastic carcinoma", "Metaplastic Breast Carcinoma", "metaplastic carcinoma of breast", "Metaplastic carcinoma of breast", "Metaplastic Carcinoma of Breast", "Metaplastic carcinoma of the breast", "Metaplastic Carcinoma of the Breast", "metaplastic carcinoma of the breast", "Metaplastic carcinoma of breast (disorder)", "metaplastic carcinoma of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metaplastic breast carcinoma", "shortest_name_length": 4}
{"curie": "UMLS:C0452047", "names": ["Focal brain injury", "Focal Brain Injury", "Brain Injury, Focal", "Injury, Focal Brain", "injury; brain, focal", "Focal Brain Injuries", "brain; injury, focal", "Brain Injuries, Focal", "Injuries, Focal Brain", "Focal brain injury (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brain Injuries, Focal", "shortest_name_length": 18}
{"curie": "MONDO:0011933", "names": ["CDG1I", "CDGIi", "CDG-Ii", "CDG Ii", "CDG 1I", "ALG2-CDG", "ALG2-CDG (CDG-II)", "CDG syndrome type Ii", "Mannosyltransferase 2 deficiency", "mannosyltransferase 2 deficiency", "congenital disorder of glycosylation Ii", "congenital disorder of glycosylation 1i", "ALG2-congenital disorder of glycosylation", "Congenital disorder of glycosylation type Ii", "Congenital disorder of glycosylation type 1I", "congenital disorder of glycosylation type 1i", "congenital disorder of glycosylation type Ii", "Congenital disorder of glycosylation type 1i", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ii", "congenital disorder of glycosylation, type Ii", "Carbohydrate deficient glycoprotein syndrome type Ii", "carbohydrate deficient glycoprotein syndrome type Ii", "carbohydrate-deficient glycoprotein syndrome type 1I", "Congenital disorder of glycosylation type 1i (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ALG2-congenital disorder of glycosylation", "shortest_name_length": 5}
{"curie": "MONDO:0054831", "names": ["CSS7", "COFFIN-SIRIS syndrome 7", "COFFIN-SIRIS SYNDROME 7", "Coffin-Siris syndrome 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Coffin-Siris syndrome 7", "shortest_name_length": 4}
{"curie": "MONDO:0013241", "names": ["SCA30", "spinocerebellar ataxia 30", "SPINOCEREBELLAR ATAXIA 30", "Spinocerebellar ataxia 30", "Spinocerebellar ataxia type 30", "spinocerebellar ataxia type 30", "SCA30 Spinocerebellar ataxia 30", "Spinocerebellar ataxia type 30 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia type 30", "shortest_name_length": 5}
{"curie": "MONDO:0006173", "names": ["Conjunctiva Epidermoid Carcinoma", "conjunctiva epidermoid carcinoma", "Conjunctival Epidermoid carcinoma", "Conjunctival Squamous Cell Cancer", "Conjunctival Epidermoid Carcinoma", "conjunctival epidermoid carcinoma", "ocular surface squamous neoplasia", "conjunctival squamous cell cancer", "Epidermoid Carcinoma of Conjunctiva", "Conjunctiva Squamous Cell Carcinoma", "conjunctiva squamous cell carcinoma", "epidermoid carcinoma of conjunctiva", "conjunctival squamous cell carcinoma", "Conjunctival Squamous Cell Carcinoma", "Squamous cell carcinoma of conjunctiva", "squamous cell carcinoma of conjunctiva", "Squamous Cell Carcinoma of Conjunctiva", "epidermoid carcinoma of the conjunctiva", "Epidermoid Carcinoma of the Conjunctiva", "Squamous Cell Carcinoma of the Conjunctiva", "squamous cell carcinoma of the conjunctiva", "conjunctival neoplasm squamous cell carcinoma", "Squamous cell carcinoma of conjunctiva (disorder)", "Squamous cell carcinoma of conjunctiva (diagnosis)", "invasive squamous cell carcinoma of the conjunctiva"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "conjunctival squamous cell carcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C1558321", "names": ["Intraoperative Breast Injury", "Intraoperative breast injury", "intraoperative breast injury", "intraoperative breast injury (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraoperative Breast Injury", "shortest_name_length": 28}
{"curie": "MONDO:0021969", "names": ["Banti syndrome", "Banti's disease", "Banti's syndrome", "[OBSOLETE] Banti's syndrome", "idiopathic portal hypertension", "idiopathic congestive splenomegaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Banti syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C0752107", "names": ["Familial Metabolic Brain Diseases", "Inherited Metabolic Brain Diseases", "Metabolic Brain Diseases, Familial", "Metabolic Brain Diseases, Inherited", "Familial Metabolic Disorders, Brain", "Brain Diseases, Metabolic, Familial", "Metabolic Disorders, Familial, Brain", "Inherited Metabolic Disorders, Brain", "Brain Diseases, Metabolic, Inherited", "Metabolic Disorders, Brain, Inherited"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brain Diseases, Metabolic, Inherited", "shortest_name_length": 33}
{"curie": "MONDO:0011050", "names": ["Ellis Yale Winter syndrome", "Ellis-Yale-Winter syndrome", "microcephaly-cardiac defect-lung malsegmentation syndrome", "Microcephaly-cardiac defect-lung malsegmentation syndrome", "Microcephaly with cardiac defect and lung malsegmentation syndrome", "Microcephalus with cardiac defect and lung malsegmentation syndrome", "Microcephalus with cardiac defect and lung malsegmentation syndrome (disorder)", "Microcephaly, Congenital Heart Disease, Unilateral Renal Agenesis, and Hyposegmented Lungs", "microcephaly, congenital heart disease, unilateral renal agenesis, and hyposegmented lungs", "MICROCEPHALY, CONGENITAL HEART DISEASE, UNILATERAL RENAL AGENESIS, AND HYPOSEGMENTED LUNGS", "microcephaly, congenital heart disease, lung segmentation defects and unilateral renal agenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly-cardiac defect-lung malsegmentation syndrome", "shortest_name_length": 26}
{"curie": "MONDO:0011241", "names": ["PSEUDOACROMEGALY WITH SEVERE INSULIN RESISTANCE", "Pseudoacromegaly with Severe Insulin Resistance", "pseudoacromegaly with severe insulin resistance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudoacromegaly with severe insulin resistance", "shortest_name_length": 47}
{"curie": "MONDO:0004607", "names": ["vallecula cancer", "epiglottic vallecula cancer", "malignant tumor of vallecula", "Malignant tumor of vallecula", "Malignant tumour of vallecula", "cancer of epiglottic vallecula", "Malignant neoplasm of vallecula", "malignant neoplasm of vallecula", "Malignant tumor of vallecula (disorder)", "malignant epiglottic vallecula neoplasm", "malignant neoplasm of epiglottic vallecula", "malignant neoplasm of vallecula (diagnosis)", "Malignant neoplasm of vallecula epiglottica"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vallecula cancer", "shortest_name_length": 16}
{"curie": "MONDO:0021287", "names": ["Stage 0 Epiglottic Carcinoma", "Epiglottis Carcinoma in situ", "stage 0 epiglottic carcinoma", "epiglottis carcinoma in situ", "Epiglottis carcinoma in situ", "epiglottic carcinoma in situ", "epiglottis in situ carcinoma", "stage 0 epiglottis carcinoma", "Epiglottic Carcinoma in situ", "carcinoma in situ of epiglottis", "Carcinoma in situ of epiglottis", "Carcinoma in situ of Epiglottis", "stage 0 epiglottic throat cancer", "Stage 0 Epiglottic Throat Cancer", "Carcinoma in situ of the Epiglottis", "Carcinoma in situ of epiglottis NOS", "carcinoma in situ of the Epiglottis", "Stage 0 Epiglottic Carcinoma AJCC v6", "Stage 0 Epiglottic Carcinoma AJCC v8", "stage 0 epiglottic carcinoma aJCC v6", "Carcinoma in situ of epiglottis, NOS", "stage 0 epiglottic carcinoma aJCC v8", "Stage 0 Epiglottic Carcinoma AJCC v7", "stage 0 epiglottic carcinoma aJCC v7", "Carcinoma in situ of epiglottis (disorder)", "Stage 0 Epiglottic Carcinoma AJCC v6, v7, and v8", "stage 0 epiglottic carcinoma aJCC v6, v7, and v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma in situ of epiglottis", "shortest_name_length": 28}
{"curie": "UMLS:C5418758", "names": ["Inherited Osteolysis Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Inherited Osteolysis Syndrome", "shortest_name_length": 29}
{"curie": "MONDO:0017171", "names": ["MPS6, rapidly progressing", "MPSVI, rapidly progressing", "arylsulfatase B deficiency, rapidly progressing", "mucopolysaccharidosis type 6, rapidly progressing", "mucopolysaccharidosis type VI, rapidly progressing"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucopolysaccharidosis type 6, rapidly progressing", "shortest_name_length": 25}
{"curie": "UMLS:C4521733", "names": ["Stage IIIA Esophageal Squamous Cell Cancer", "Postneoadjuvant Therapy Stage IIIA Esophageal Squamous Cell Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postneoadjuvant Therapy Stage IIIA Esophageal Squamous Cell Carcinoma AJCC v8", "shortest_name_length": 42}
{"curie": "UMLS:C2584556", "names": ["drug-induced interstitial nephritis", "INTERSTITIAL NEPHRITIS DRUG INDUCED", "Drug-induced interstitial nephritis", "Drug-induced tubulointerstitial nephritis", "Drug-Induced Tubulointerstitial Nephritis", "drug-induced interstitial nephritis (diagnosis)", "Drug-induced tubulointerstitial nephritis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drug-induced tubulointerstitial nephritis", "shortest_name_length": 35}
{"curie": "UMLS:C3899665", "names": ["Epithelioid Hemangioendothelioma", "childhood epithelioid hemangioendothelioma", "Childhood Epithelioid Hemangioendothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Epithelioid Hemangioendothelioma", "shortest_name_length": 32}
{"curie": "MONDO:0009569", "names": ["Hennekam-Beemer syndrome", "Hennekam Beemer syndrome", "Mastocytosis-short stature-deafness syndrome", "Mastocytosis-short stature-hearing loss syndrome", "mastocytosis-short stature-hearing loss syndrome", "Cutaneous mastocytosis, short stature, hearing loss syndrome", "cutaneous mastocytosis, conductive hearing loss and microtia", "CUTANEOUS MASTOCYTOSIS, CONDUCTIVE HEARING LOSS AND MICROTIA", "Cutaneous mastocytosis, short stature, hearing loss syndrome (disorder)", "mastocytosis cutaneous with short stature conductive hearing loss and microtia", "Mastocytosis, cutaneous, with short stature, conductive hearing loss and microtia", "skin mastocytosis hearing loss microcephaly mild dysmorphic features and severe mental retardation", "skin mastocytosis hearing loss microcephaly mild dysmorphic features and severe intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hennekam-Beemer syndrome", "shortest_name_length": 24}
{"curie": "UMLS:C5418898", "names": ["Locally Advanced Chondrosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Chondrosarcoma", "shortest_name_length": 31}
{"curie": "UMLS:C0877417", "names": ["Cytomegalovirus enterocolitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cytomegalovirus enterocolitis", "shortest_name_length": 29}
{"curie": "MONDO:0000605", "names": ["Sensitive", "sensitive", "sensitivity", "Sensitivity", "Hypersensitive", "hypersensitive", "hypersensitivity", "Hypersensitivity", "Allergic reaction", "allergic reaction", "hypersensitivity reaction", "Hypersensitivity Reaction", "Hypersensitivity condition", "hypersensitivity reaction disease", "Hypersensitivity/Allergic reaction", "Hypersensitivity condition (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypersensitivity reaction disease", "shortest_name_length": 9}
{"curie": "UMLS:C3179058", "names": ["Corpus Callosum Malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Corpus Callosum Malformation", "shortest_name_length": 28}
{"curie": "UMLS:C1336719", "names": ["Testicular Mixed Germ Cell-Sex Cord Tumor", "Testicular Mixed Germ Cell-Sex Cord Neoplasm", "Testicular Mixed Germ Cell-Sex Cord-Stromal Tumor", "Testicular Mixed Germ Cell-Sex Cord-Stromal Neoplasm", "Testicular Mixed Germ Cell-Sex Cord-Stromal Tumor, Unclassified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular Mixed Germ Cell-Sex Cord-Stromal Tumor", "shortest_name_length": 41}
{"curie": "MONDO:0008578", "names": ["TOE, ROTATED FIFTH", "toe, rotated fifth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "toe, rotated fifth", "shortest_name_length": 18}
{"curie": "MONDO:0007917", "names": ["LYMPHEDEMA AND CEREBRAL ARTERIOVENOUS ANOMALY", "lymphedema and cerebral arteriovenous anomaly", "Lymphedema and Cerebral Arteriovenous Anomaly", "lymphedema-cerebral arteriovenous anomaly syndrome", "primary pulmonary hypertension, cerebrovascular malformation and lymphedema feet"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphedema-cerebral arteriovenous anomaly syndrome", "shortest_name_length": 45}
{"curie": "MONDO:0012708", "names": ["PLSA", "PLSA1", "PLS, ADULT", "Pls, adult", "PLS, Adult", "PRIMARY LATERAL SCLEROSIS, ADULT, 1", "primary lateral sclerosis, adult, 1", "Primary Lateral Sclerosis, Adult, 1", "primary lateral sclerosis, ADULT, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary lateral sclerosis, adult, 1", "shortest_name_length": 4}
{"curie": "UMLS:C5447242", "names": ["Breast Neurofibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Neurofibroma", "shortest_name_length": 19}
{"curie": "UMLS:C5237066", "names": ["Very High Risk Myelodysplastic Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Very High Risk Myelodysplastic Syndrome", "shortest_name_length": 39}
{"curie": "UMLS:C1450051", "names": ["EDMD3", "Autosomal Recessive Emery Dreifuss Muscular Dystrophy", "Autosomal Recessive Emery-Dreifuss Muscular Dystrophy", "Autosomal recessive Emery-Dreifuss muscular dystrophy", "Emery Dreifuss Muscular Dystrophy, Autosomal Recessive", "Emery-Dreifuss Muscular Dystrophy, Autosomal Recessive", "Muscular Dystrophy, Emery-Dreifuss, Autosomal Recessive", "EDMD3 - autosomal recessive Emery-Dreifuss muscular dystrophy", "Autosomal recessive Emery-Dreifuss muscular dystrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Autosomal Recessive Emery-Dreifuss Muscular Dystrophy", "shortest_name_length": 5}
{"curie": "MONDO:0024292", "names": ["GI Polyp", "GI polyp", "Intestinal polyposis", "Gastrointestinal Polyp", "Gastrointestinal polyp", "gastrointestinal polyp", "GASTROINTESTINAL POLYP", "Gastrointestinal polyps", "gastrointestinal polyps", "Multiple intestinal polyps", "Gastrointestinal Tract Polyp", "gastrointestinal tract polyp", "Growths in inner lining of intestine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastrointestinal polyp", "shortest_name_length": 8}
{"curie": "MONDO:0007028", "names": ["rotator cuff tear", "Rotator cuff tear", "Rotator cuff rupture", "IMPINGEMENT SYNDROME", "Impingement syndrome", "impingement syndrome", "cuff rotator syndrome", "ROTATOR CUFF SYNDROME", "syndrome; impingement", "rotator cuff syndrome", "syndrome rotator cuff", "impingement; syndrome", "Rotator cuff syndrome", "syndrome; rotator cuff", "rotator cuff; syndrome", "Rotator cuff syndrome NOS", "Rotator cuff syndrome, NOS", "impingement syndrome (diagnosis)", "Rotator cuff syndrome (diagnosis)", "Rupture of rotator cuff of shoulder", "disorder tendon shoulder rotator cuff syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rotator cuff syndrome", "shortest_name_length": 17}
{"curie": "MONDO:0014649", "names": ["MRT50", "mental retardation, autosomal recessive 50", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 50", "mental retardation, autosomal recessive type 50", "intellectual disability, autosomal recessive 50", "intellectual disability, autosomal recessive type 50", "autosomal recessive intellectual developmental disorder 50", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 50", "intellectual developmental disorder, autosomal recessive 50", "EDC3 autosomal recessive non-syndromic intellectual disability", "autosomal recessive non-syndromic intellectual disability caused by mutation in EDC3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 50", "shortest_name_length": 5}
{"curie": "UMLS:C0751365", "names": ["Cancer, Embryonal and Mixed"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cancer, Embryonal and Mixed", "shortest_name_length": 27}
{"curie": "MONDO:0003122", "names": ["Striatonigral atrophy", "Striatonigral Atrophy", "Atrophy, Striatonigral", "Striatonigral Atrophies", "Atrophies, Striatonigral", "striatonigral degeneration", "Striatonigral Degeneration", "Striatonigral degeneration", "Degeneration, Striatonigral", "striatonigral; degeneration", "Striatonigral Degenerations", "degeneration; striatonigral", "SND - Striatonigral degeneration", "Striatonigral degeneration (disorder)", "striatonigral degeneration (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "striatonigral degeneration", "shortest_name_length": 21}
{"curie": "MONDO:0000597", "names": ["Meadow's syndrome", "Munchausen by proxy", "Munchausen's by proxy", "Münchausen's by proxy", "munchausen's by proxy", "munchausen syndrome proxy", "munchausen proxy syndrome", "Munchausen Syndrome by Proxy", "Munchausen syndrome by proxy", "Munchausen by proxy syndrome", "munchausen by proxy syndrome", "munchausen syndrome by proxy", "Münchausen syndrome by proxy", "syndrome munchausen by proxy", "Triggered by an abusive adult", "Munchausen syndrome by proxy (disorder)", "Munchausen syndrome by proxy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Munchausen by proxy", "shortest_name_length": 17}
{"curie": "MONDO:0012974", "names": ["DFNA59", "autosomal dominant deafness 59", "DEAFNESS, AUTOSOMAL DOMINANT 59", "deafness, autosomal dominant 59", "Deafness, Autosomal Dominant 59", "DEAFNESS, AUTOSOMAL DOMINANT 59 (disorder)", "autosomal dominant nonsyndromic deafness 59", "autosomal dominant nonsyndromic hearing loss 59", "autosomal dominant nonsyndromic deafness type 59"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 59", "shortest_name_length": 6}
{"curie": "MONDO:0019770", "names": ["X-linked dominant intellectual disability-epilepsy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked dominant intellectual disability-epilepsy syndrome", "shortest_name_length": 59}
{"curie": "UMLS:C4553784", "names": ["Stage 0is Renal Pelvis and Ureter Cancer", "stage 0is renal pelvis and ureter cancer AJCC v8", "Stage 0is Renal Pelvis and Ureter Cancer AJCC v8", "stage 0is renal pelvis and ureter urothelial carcinoma AJCC v8", "Stage 0is Renal Pelvis and Ureter Urothelial Carcinoma AJCC v8", "stage 0is transitional cell cancer of the renal pelvis and ureter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0is Renal Pelvis and Ureter Cancer AJCC v8", "shortest_name_length": 40}
{"curie": "MONDO:0008973", "names": ["Toriello Higgins Miller syndrome", "Toriello-Higgins-Miller syndrome", "CHONDRODYSPLASIA PUNCTATA SYNDROME", "chondrodysplasia punctata syndrome", "Chondrodysplasia Punctata Syndrome", "Chondrodysplasia punctata Toriello type", "Chondrodysplasia punctata, Toriello type", "chondrodysplasia punctata, Toriello type", "Chondrodysplasia punctata Toriello type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chondrodysplasia punctata, Toriello type", "shortest_name_length": 32}
{"curie": "MONDO:0015160", "names": ["MCA/variable MR", "multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome", "multiple congenital anomalies-variable intellectual disability with or without dysmorphism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0005929", "names": ["baby blues", "Baby Blues", "Baby blues", "blue maternity", "Third day blues", "Maternity blues", "Postnatal blues", "maternity blues", "postnatal blues", "Depression;postnatal", "postnatal depression", "Depression;puerperal", "depression postnatal", "Puerperal Depression", "DEPRESSION PUERPERAL", "Puerperal depression", "Depression puerperal", "Postnatal depression", "puerperal depression", "Postnatal Depression", "Postpartum depression", "depression; postnatal", "post natal depression", "post Natal depression", "depression, postnatal", "postnatal; depression", "post-Natal depression", "post-natal depression", "Postpartum Depression", "Post Natal Depression", "postpartum depression", "depression postpartum", "Post-Natal Depression", "Depression, Postnatal", "DEPRESSION POSTPARTUM", "Depression, Postpartum", "Post-Partum Depression", "Post Partum Depression", "postpartum; depression", "depression; postpartum", "post-partum depression", "Depression, Post-Natal", "post partum depression", "depression, post-Natal", "depression, post-partum", "Depression, Post-Partum", "Post-pregnancy depression", "Postnatal depression, NOS", "Maternity blues (disorder)", "Postpartum depression, NOS", "Maternity blues (diagnosis)", "Postnatal depressive disorder", "Postpartum depression (disorder)", "postpartum depression (diagnosis)", "Postnatal depression (excl psychosis)", "postpartum depression maternity blues", "depressive episode with postpartum onset", "Depressive Episode with Postpartum Onset", "Postnatal depression (excluding psychosis)", "Major Depressive Episode with Peripartum Onset", "major depressive episode with peripartum onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postpartum depression", "shortest_name_length": 10}
{"curie": "MONDO:0033948", "names": ["acquired angioedema with C1Inh deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired angioedema with C1Inh deficiency", "shortest_name_length": 41}
{"curie": "MONDO:0009259", "names": ["glutamate-cysteine ligase deficiency", "Glutamate-cysteine ligase deficiency", "Deficiency of glutamate-cysteine ligase", "Gamma-glutamyl cysteine synthase deficiency", "gamma-Glutamylcysteine synthetase deficiency", "gamma-glutamylcysteine synthetase deficiency", "Gamma-glutamylcysteine synthetase deficiency", "Glutamate-cysteine ligase deficiency (disorder)", "inborn error of glutamate-cysteine ligase activity", "inborn glutamate-cysteine ligase activity disorder", "rare inborn error of glutamate-cysteine ligase activity", "hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency", "gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to", "GAMMA-GLUTAMYLCYSTEINE SYNTHETASE DEFICIENCY, HEMOLYTIC ANEMIA DUE TO", "Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gamma-glutamylcysteine synthetase deficiency", "shortest_name_length": 36}
{"curie": "UMLS:C0263370", "names": ["Digitate dermatosis", "Small Plaque Parapsoriasis", "small plaque parapsoriasis", "parapsoriasis small plaque", "Small plaque parapsoriasis", "parapsoriasis; small plaque", "small plaque; parapsoriasis", "Chronic superficial dermatitis", "Chronic superficial scaly dermatitis", "Small plaque parapsoriasis (disorder)", "small plaque parapsoriasis (diagnosis)", "Persistent superficial scaly dermatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small plaque parapsoriasis", "shortest_name_length": 19}
{"curie": "MONDO:0014386", "names": ["BDPLT18", "platelet-type bleeding disorder 18", "BLEEDING DISORDER, PLATELET-TYPE, 18", "bleeding disorder, platelet-type, 18", "bleeding disorder due to CalDAG-GEFI deficiency", "RASGRP2 inherited bleeding disorder, platelet-type", "inherited bleeding disorder, platelet-type caused by mutation in RASGRP2", "bleeding disorder due to calcium- and DAG-regulated guanine exchange factor-1 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "platelet-type bleeding disorder 18", "shortest_name_length": 7}
{"curie": "UMLS:C5205968", "names": ["Seminal Vesicle Leiomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Seminal Vesicle Leiomyosarcoma", "shortest_name_length": 30}
{"curie": "MONDO:0005108", "names": ["virus", "Viral illness", "virus disease", "viral illness", "Viral disease", "Viral Disease", "Virus Disease", "viral disease", "viral; disease", "Disease, Virus", "Virus Diseases", "viral disorder", "Viral Diseases", "VIRAL DISEASES", "Viral Disorder", "Virus diseases", "Disease, Viral", "viral diseases", "Viral infection", "Virus Infection", "Infection;viral", "Diseases, Viral", "Viral Disorders", "viral infection", "virus infection", "Viral Infection", "VIRAL INFECTION", "Infection viral", "INFECTION VIRAL", "Diseases, Virus", "viral; infection", "Infection, Virus", "infection; virus", "Viral infections", "infection; viral", "Virus Infections", "virus; infection", "Infection, Viral", "infection, viral", "Viral Infections", "Viruses infection", "Infections, Virus", "Infections, Viral", "Viral disease, NOS", "Viral illness, NOS", "Viral infection NOS", "viral infection nos", "infections, Viruses", "Viral infection, NOS", "Disease due to virus", "Disease caused by virus", "Viral disease (disorder)", "Viral infectious disease", "viral infectious disease", "Viral Infectious Disease", "diseases caused by viruses", "Viruses infectious disease", "Diseases Caused by Viruses", "viral infection (diagnosis)", "Viruses disease or disorder", "Viral infection, unspecified", "Disease caused by virus, NOS", "Viral infectious disease, NOS", "VIRAL DISEASES: GENERAL TERMS", "viral; infection, unspecified site", "infection; viral, unspecified site", "Viruses caused disease or disorder", "Viral infection of unspecified site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "viral infectious disease", "shortest_name_length": 5}
{"curie": "MONDO:0021950", "names": ["autoimmune oophoritis", "Autoimmune oophoritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune oophoritis", "shortest_name_length": 21}
{"curie": "MONDO:0000584", "names": ["BLNK deficiency", "agammaglobulinemia 4", "B-cell linker protein deficiency", "B cell linker protein deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B cell linker protein deficiency", "shortest_name_length": 15}
{"curie": "MONDO:0013719", "names": ["CED4", "CRANIOECTODERMAL DYSPLASIA 4", "cranioectodermal dysplasia 4", "cranioectodermal dysplasia type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cranioectodermal dysplasia 4", "shortest_name_length": 4}
{"curie": "MONDO:0015835", "names": ["Bicervical bicornuate uterus and blind hemivagina"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bicervical bicornuate uterus and blind hemivagina", "shortest_name_length": 49}
{"curie": "UMLS:C0855116", "names": ["Stage IV Diffuse Large B-Cell Lymphoma", "Diffuse Large B-Cell Lymphoma Stage IV", "Diffuse large B-cell lymphoma stage IV", "Ann Arbor Stage IV Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Diffuse Large B-Cell Lymphoma", "shortest_name_length": 38}
{"curie": "MONDO:0014798", "names": ["BDA1D", "brachydactyly type A1D", "BRACHYDACTYLY, TYPE A1, D", "brachydactyly, type A1, D", "BMPR1B brachydactyly type A1", "brachydactyly type A1 caused by mutation in BMPR1B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly type A1D", "shortest_name_length": 5}
{"curie": "MONDO:0001834", "names": ["optic tract disease", "optic tract disorder", "Optic tract disorder", "disease of optic tract", "visual pathway disease", "Disorder of optic tract", "Visual Pathway Disorder", "disorder of optic tract", "Visual pathway disorder", "visual pathway disorder", "Visual pathway disorders", "Disorder of visual pathways", "Visual pathway disorder NOS", "Disorder of optic tract, NOS", "optic tract disease or disorder", "Disorder of visual pathways, NOS", "DISORDERS OF THE VISUAL PATHWAYS", "disease or disorder of optic tract", "Disorder of optic tract (disorder)", "Disorder of afferent visual pathways", "Disorder of visual pathways (disorder)", "disease (or disorder); visual pathways", "Unspecified disorder of visual pathways", "Disorder of visual pathways, unspecified", "Disorder of optic nerve and visual pathway", "Disorders of optic nerve and visual pathways", "Disorders of optic nerve and visual pathways (H46-H47)", "Unspecified disorder of optic nerve and visual pathways"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "visual pathway disorder", "shortest_name_length": 19}
{"curie": "UMLS:C5446442", "names": ["Lacrimal Drainage System Exophytic Papilloma", "Exophytic Papilloma of the Lacrimal Drainage System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lacrimal Drainage System Exophytic Papilloma", "shortest_name_length": 44}
{"curie": "UMLS:C4330380", "names": ["Hypopharyngeal Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypopharyngeal Carcinoma by AJCC v8 Stage", "shortest_name_length": 41}
{"curie": "UMLS:C0205707", "names": ["sprue", "Sprue", "SPRUE", "sprues", "Sprue NOS", "Sprue, NOS", "Sprue (disorder)", "sprue (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sprue", "shortest_name_length": 5}
{"curie": "MONDO:0002990", "names": ["Deep histiocytoma", "Deep Fibrous Histiocytoma", "Deep benign fibrous histiocytoma", "deep benign fibrous histiocytoma", "Benign Deep Fibrous Histiocytoma", "benign deep fibrous histiocytoma", "Deep Benign Fibrous Histiocytoma", "Deep histiocytoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign deep fibrous histiocytoma", "shortest_name_length": 17}
{"curie": "UMLS:C0555202", "names": ["Mantle zone lymphoma", "Malignant lymphoma, lymphocytic, intermediate differentiation", "malignant lymphoma, lymphocytic, intermediate differentiation", "Malignant lymphoma - lymphocytic, intermediate differentiation", "malignant neoplasm lymphoma, lymphocytic, intermediate differentiation", "Malignant lymphoma - lymphocytic, intermediate differentiation (disorder)", "malignant lymphoma, lymphocytic, intermediate differentiation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant lymphoma - lymphocytic, intermediate differentiation", "shortest_name_length": 20}
{"curie": "MONDO:0007520", "names": ["EEC", "EEC1", "EEC syndrome-1", "EEC Syndrome 1", "EEC syndrome 1", "EEC SYNDROME 1", "ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1", "Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip-Palate Syndrome 1", "ectrodactyly, ectodermal dysplasia, and cleft LIP/palate syndrome 1", "ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 1", "ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1", "shortest_name_length": 3}
{"curie": "MONDO:0002889", "names": ["orbit cancer", "orbital tumor", "orbital cancer", "malignant orbit tumor", "orbit of skull cancer", "Malignant Orbit Tumor", "Malignant orbital tumor", "Malignant Orbital Tumor", "malignant orbital tumor", "malignant orbit neoplasm", "Malignant Tumor of Orbit", "cancer of orbit of skull", "neoplasm of orbit proper", "Malignant orbital tumour", "Malignant Orbit Neoplasm", "Malignant tumor of orbit", "malignant tumor of orbit", "Malignant tumour of orbit", "Malignant Orbital Neoplasm", "malignant orbital neoplasm", "malignant neoplasm of orbit", "Malignant Neoplasm of Orbit", "Malignant neoplasm of orbit", "Malignant Tumor of the Orbit", "malignant tumor of the orbit", "malignant neoplasm of the orbit", "Malignant Neoplasm of the Orbit", "malignant orbit of skull neoplasm", "Malignant tumor of orbit (disorder)", "malignant neoplasm of orbit of skull", "malignant neoplasm of orbit (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orbital cancer", "shortest_name_length": 12}
{"curie": "MONDO:0004731", "names": ["central apnea", "central Apneas", "apnea, central", "Apneas, central", "ondine syndrome", "central sleep apnea", "Central sleep apnea", "apnea, central sleep", "Sleep Apnea, Central", "Central sleep apnoea", "central sleep Apneas", "Apneas, central sleep", "sleep Apneas, central", "apnea, sleep, central", "CSA - Central sleep apnea", "CSA - Central sleep apnoea", "sleep apnea, lethal central", "primary central sleep apnea", "central sleep apnea, primary", "Central Sleep Apnea Syndrome", "central sleep apnea syndrome", "Central sleep apnea syndrome", "secondary central sleep apnea", "Central sleep apnoea syndrome", "central sleep apnea, secondary", "central alveolar hypoventilation", "hypoventilation, central alveolar", "alveolar hypoventilation, central", "hypoventilations, central alveolar", "central sleep-disordered breathing", "central sleep disordered breathing", "alveolar hypoventilations, central", "breathing, central sleep-disordered", "sleep-disordered breathing, central", "central sleep-disordered Breathings", "sleep disordered breathing, central", "Breathings, central sleep-disordered", "sleep-disordered Breathings, central", "Central sleep apnea syndrome (disorder)", "central alveolar hypoventilation syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central sleep apnea syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0012989", "names": ["MCPH7", "primary autosomal recessive microcephaly 7", "MICROCEPHALY 7, PRIMARY, AUTOSOMAL RECESSIVE", "Microcephaly, Primary Autosomal Recessive, 7", "microcephaly 7, primary, autosomal recessive", "STIL autosomal recessive primary microcephaly", "MICROCEPHALY, PRIMARY AUTOSOMAL RECESSIVE, 7 (disorder)", "autosomal recessive primary microcephaly caused by mutation in STIL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly 7, primary, autosomal recessive", "shortest_name_length": 5}
{"curie": "MONDO:0017967", "names": ["Anorchia", "anorchia", "Anorchism", "anorchism", "Anorchidism", "anorchidism", "empty scrotum", "Empty scrotum", "Male agonadism", "absence of testes", "Absence of testes", "Bilateral anorchia", "bilateral anorchia", "Testicular agenesis", "testicular agenesis", "anorchia (diagnosis)", "Congenital absent testes", "congenital absence of testes", "Congenital anorchia syndrome", "Testicular agenesis, bilateral", "Congenital absence of both testes", "Bilateral congenital aplasia of testicles", "Congenital absence of both testes (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular agenesis", "shortest_name_length": 8}
{"curie": "UMLS:C1882277", "names": ["pancreatic G-cell adenoma", "Pancreatic G-Cell Adenoma", "gastrin secreting adenoma", "gastrin producing adenoma", "G-cell adenoma, pancreatic", "adenoma, pancreatic G-cell", "G-cell, pancreatic adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic G-Cell Adenoma", "shortest_name_length": 25}
{"curie": "MONDO:0017276", "names": ["FTD", "WLD", "MSTD", "PPND", "FLDEM", "HDDD1", "HDDD2", "DDPAC", "FTDP17", "FTD-GRN", "FTDP-17", "FTD-PGRN", "FTLD-TDP", "FTLD-17 GRN", "Familial Pick Disease", "Familial Picks Disease", "FRONTOTEMPORAL DEMENTIA", "Frontotemporal dementia", "frontotemporal dementia", "Familial Pick's Disease", "Frontotemporal Dementia", "dementia frontotemporal", "Wilhemsen-Lynch disease", "WILHELMSEN-LYNCH DISEASE", "Wilhelmsen-Lynch Disease", "Disease, Familial Pick's", "Pick's Disease, Familial", "Wilhelmsen Lynch Disease", "DEMENTIA, FRONTOTEMPORAL", "Familial Pick's Diseases", "Frontotemporal Dementias", "Dementia, Frontotemporal", "FTLD WITH TAU INCLUSIONS", "Wilhelmsen-Lynch Diseases", "Pick's Diseases, Familial", "Diseases, Familial Pick's", "Dementias, Frontotemporal", "Disease, Wilhelmsen-Lynch", "FTLD with TDP-43 Pathology", "Diseases, Wilhelmsen-Lynch", "FTLD with TDP 43 Pathology", "Frontotemporal Lobe Dementia", "FRONTOTEMPORAL LOBE DEMENTIA", "Frontotemporal Lobe Dementias", "Dementia, Frontotemporal Lobe", "Lobe Dementia, Frontotemporal", "Lobe Dementias, Frontotemporal", "Dementias, Frontotemporal Lobe", "Pallidopontonigral degeneration", "PALLIDOPONTONIGRAL DEGENERATION", "pallidopontonigral degeneration", "Pallidopontonigral Degeneration", "frontotemporal lobar degeneration", "Frontotemporal dementia (disorder)", "frontotemporal dementia (diagnosis)", "GRN-Related Frontotemporal Dementia", "GRN Related Frontotemporal Dementia", "frontotemporal lobe dementia (FLDEM)", "Frontotemporal Dementia, GRN-Related", "Dementia, GRN-Related Frontotemporal", "GRN-Related Frontotemporal Dementias", "Frontotemporal Lobe Dementia (FLDEM)", "Frontotemporal Lobe Dementias (FLDEM)", "Frontotemporal Dementias, GRN-Related", "Dementia, Frontotemporal Lobe (FLDEM)", "Dementias, GRN-Related Frontotemporal", "Dementias, Frontotemporal Lobe (FLDEM)", "Frontotemporal Dementia with Parkinsonism", "FRONTOTEMPORAL DEMENTIA WITH PARKINSONISM", "Ubiquitin-Positive Frontotemporal Dementia", "Pallidopontonigral degeneration (disorder)", "Ubiquitin-Positive Frontotemporal Dementias", "Hereditary Dysphasic Disinhibition Dementia", "DEMENTIA, FRONTOTEMPORAL, WITH PARKINSONISM", "Frontotemporal Dementia, Ubiquitin-Positive", "Dementia, Ubiquitin-Positive Frontotemporal", "Frontotemporal Dementia, Ubiquitin Positive", "Dementia, Frontotemporal, with Parkinsonism", "Frontotemporal Dementia with Parkinsonism 17", "Frontotemporal Dementias, Ubiquitin-Positive", "Frontotemporal Dementia with Parkinsonism-17", "Dementias, Ubiquitin-Positive Frontotemporal", "Dementia, Hereditary Dysphasic Disinhibition", "Multiple System Tauopathy with Presenile Dementia", "multiple system tauopathy with presenile dementia", "MULTIPLE SYSTEM TAUOPATHY WITH PRESENILE DEMENTIA", "Disinhibition-Dementia-Parkinsonism-Amytrophy Complex", "FRONTOTEMPORAL LOBAR DEGENERATION WITH TAU INCLUSIONS", "Disinhibition Dementia Parkinsonism Amytrophy Complex", "Disinhibition Dementia Parkinsonism Amyotrophy Complex", "Disinhibition-Dementia-Parkinsonism-Amyotrophy Complex", "DISINHIBITION-DEMENTIA-PARKINSONISM-AMYOTROPHY COMPLEX", "Complex, Disinhibition-Dementia-Parkinsonism-Amytrophy", "Disinhibition-Dementia-Parkinsonism-Amytrophy Complices", "Complex, Disinhibition-Dementia-Parkinsonism-Amyotrophy", "Complices, Disinhibition-Dementia-Parkinsonism-Amytrophy", "Disinhibition-Dementia-Parkinsonism-Amyotrophy Complices", "Complices, Disinhibition-Dementia-Parkinsonism-Amyotrophy", "Frontotemporal Lobar Degeneration With Ubiquitin-Positive Inclusions", "Frontotemporal Lobar Degeneration With Ubiquitin Positive Inclusions", "FRONTOTEMPORAL LOBAR DEGENERATION WITH UBIQUITIN-POSITIVE INCLUSIONS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontotemporal dementia", "shortest_name_length": 3}
{"curie": "MONDO:0012939", "names": ["DBA8", "Diamond-Blackfan anemia 8", "DIAMOND-BLACKFAN ANEMIA 8", "Diamond-Blackfan Anemia 8", "RPS7 Diamond-Blackfan anemia", "Diamond-Blackfan Anemia type 8", "RPS7-related Diamond-Blackfan anemia", "Diamond-Blackfan anemia caused by mutation in RPS7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diamond-Blackfan anemia 8", "shortest_name_length": 4}
{"curie": "MONDO:0003091", "names": ["mucoepidermoid skin carcinoma", "Mucoepidermoid skin carcinoma", "Mucoepidermoid Skin Carcinoma", "Mucoepidermal eccrine carcinoma", "Mucoepidermoid Carcinoma of Skin", "mucoepidermoid carcinoma of skin", "Mucoepidermoid carcinoma of skin", "cutaneous mucoepidermoid carcinoma", "Mucoepidermoid Carcinoma of the Skin", "zone of skin mucoepidermoid carcinoma", "Primary mucoepidermoid carcinoma of skin", "Mucoepidermoid carcinoma of skin (disorder)", "mucoepidermoid carcinoma of skin (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous mucoepidermoid carcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0023577", "names": ["Krieble Bixler syndrome", "autosomal dominant blepharophimosis with multiple congenital anomalies", "Autosomal dominant blepharophimosis with multiple congenital anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Krieble Bixler syndrome", "shortest_name_length": 23}
{"curie": "UMLS:C4330257", "names": ["Hereditary Factor III Deficiency", "Hereditary Tissue Factor Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hereditary Factor III Deficiency", "shortest_name_length": 32}
{"curie": "MONDO:0012642", "names": ["BPAD", "MAFD4", "Major Affective Disorder 4", "BIPOLAR AFFECTIVE DISORDER", "major affective disorder 4", "bipolar affective disorder", "MAJOR affective disorder 4", "MAJOR AFFECTIVE DISORDER 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "major affective disorder 4", "shortest_name_length": 4}
{"curie": "MONDO:0018260", "names": ["scalp syndrome", "sebaceous nevus-CNS malformations-aplasia cutis congenital-limbal dermoid-pigmented nevus syndrome", "sebaceous nevus-central nervous system malformations-aplasia cutis congenital-limbal dermoid-pigmented nevus syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scalp syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0013431", "names": ["MGORS4", "Meier-GORLIN syndrome 4", "MEIER-GORLIN SYNDROME 4", "Meier-Gorlin syndrome 4", "CDT1 Meier-Gorlin syndrome", "Meier-Gorlin syndrome type 4", "Meier-Gorlin syndrome caused by mutation in CDT1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meier-Gorlin syndrome 4", "shortest_name_length": 6}
{"curie": "UMLS:C4285818", "names": ["Reduced facial expression"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reduced facial expression", "shortest_name_length": 25}
{"curie": "UMLS:C5420648", "names": ["Recurrent Vulvar Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Vulvar Squamous Cell Carcinoma", "shortest_name_length": 40}
{"curie": "UMLS:C4687516", "names": ["Mediastinal Mixed Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mediastinal Mixed Germ Cell Tumor", "shortest_name_length": 33}
{"curie": "MONDO:0020549", "names": ["IHM", "Invasive mole", "Chorioadenoma", "invasive Mole", "Invasive Mole", "invasive mole", "chorioadenoma", "malignant mole", "Mole;malignant", "Chorioadenomas", "mole; invasive", "Invasive Moles", "invasive; mole", "MOLE, INVASIVE", "Mole, Invasive", "MOLE, MALIGNANT", "malignant moles", "Moles, Invasive", "[M]Chorioadenoma", "MOLE, DESTRUCTIVE", "destructive; mole", "mole; destructive", "IM - Invasive mole", "Invasive mole, NOS", "GTT, invasive mole", "Malignant hydatid mole", "chorioadenoma destruens", "Chorioadenoma destruens", "CHORIOADENOMA DESTRUENS", "chorioadenoma Destruens", "Chorioadenoma Destruens", "Invasive mole - placenta", "[M]Chorioadenoma destruens", "invasive hydatidiform mole", "Invasive hydatidiform mole", "Invasive Hydatidiform Mole", "invasive hydatidiform Mole", "Mole, Invasive Hydatidiform", "Invasive Hydatidiform Moles", "Hydatidiform mole malignant", "Hydatidiform Mole, Invasive", "Malignant hydatidiform mole", "invasive; hydatidiform mole", "hydatidiform mole; invasive", "Hydatidiform Moles, Invasive", "hydatidiform mole; malignant", "malignant; hydatidiform mole", "mole; hydatidiform, invasive", "Moles, Invasive Hydatidiform", "[M]Invasive hydatidiform mole", "mole; hydatidiform, malignant", "malignant; mole, hydatidiform", "Molar pregnancy with chorioadenoma", "mole; malignant, hydatidiform mole", "Molar pregnancy with invasive mole", "Invasive hydatidiform mole (disorder)", "invasive hydatidiform mole (diagnosis)", "invasive gestational trophoblastic neoplasm", "Invasive Gestational Trophoblastic Neoplasm", "Molar pregnancy with chorioadenoma destruens", "gestational trophoblastic tumor, invasive mole", "molar pregnancy, invasive (non-metastatic GTD)", "Molar pregnancy with invasive hydatidiform mole", "Molar pregnancy with malignant hydatidiform mole", "Invasive hydatidiform mole (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "invasive hydatidiform mole", "shortest_name_length": 3}
{"curie": "UMLS:C1332930", "names": ["Chest Wall Fibromatosis", "Chest Wall Desmoid Tumor", "Chest Wall Desmoid Neoplasm", "Desmoid Tumor of Chest Wall", "Desmoid Neoplasm of Chest Wall", "Desmoid Tumor of the Chest Wall", "Desmoid Neoplasm of the Chest Wall"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chest Wall Fibromatosis", "shortest_name_length": 23}
{"curie": "MONDO:0010726", "names": ["RTS", "Rts", "RTT", "Rett", "RETT SYNDROME", "Rett disorder", "Rett Syndrome", "rett disorder", "syndrome rett", "rett syndrome", "Rett syndrome", "Rett Disorder", "disorder retts", "retts syndrome", "Retts syndrome", "Retts Syndrome", "Syndrome, Rett", "rett's disorder", "Rett's Disorder", "rett's syndrome", "Rett's syndrome", "Rett's disorder", "Rett's Syndrome", "Syndrome, Rett's", "RTS - Rett syndrome", "Rett syndrome (RS, RTS)", "Rett syndrome, atypical", "Rett's disorder (disorder)", "Rett's syndrome (diagnosis)", "Cerebroatrophic hyperammonemia", "Cerebroatrophic Hyperammonemia", "cerebroatrophic hyperammonemia", "Cerebroatrophic Hyperammonemias", "Hyperammonemia, Cerebroatrophic", "Rett Syndrome, Zappella Variant", "Rett syndrome, Zappella variant", "RETT SYNDROME, ZAPPELLA VARIANT", "Cerebroatrophic hyperammonaemia", "Hyperammonemias, Cerebroatrophic", "rett syndrome, X-linked dominant", "Rett syndrome, preserved speech variant", "RETT SYNDROME, PRESERVED SPEECH VARIANT", "Rett Syndrome, Preserved Speech Variant", "rett syndrome, atypical, X-linked dominant", "autism, dementia, ataxia, and loss of purposeful hand use", "AUTISM, DEMENTIA, ATAXIA, AND LOSS OF PURPOSEFUL HAND USE", "Autism, Dementia, Ataxia, and Loss of Purposeful Hand Use", "rett syndrome, preserved speech variant, X-linked dominant", "Autism Dementia Ataxia Loss of Purposeful Hand Use Syndrome", "autism-dementia-ataxia-loss of purposeful hand use syndrome", "Autism-Dementia-Ataxia-Loss of Purposeful Hand Use Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rett syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0018636", "names": ["TPPII deficiency", "triangle disease", "tripeptidyl-peptidase II deficiency", "Evans syndrome associated with primary immunodeficiency", "autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome", "TPPII-related immunodeficiency, autoimmunity, and neurodevelopmental delay with impaired glycolysis and lysosomal expansion disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome", "shortest_name_length": 16}
{"curie": "UMLS:C1837092", "names": ["Myasthenic Syndrome, Congenital, with Facial Dysmorphism, associated with Acetylcholine Receptor Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myasthenic Syndrome, Congenital, with Facial Dysmorphism, associated with Acetylcholine Receptor Deficiency", "shortest_name_length": 107}
{"curie": "UMLS:C5556717", "names": ["Advanced Vaginal Squamous Cell Carcinoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Vaginal Squamous Cell Carcinoma, Not Otherwise Specified", "shortest_name_length": 65}
{"curie": "MONDO:0012274", "names": ["AMD3", "AMDD", "acromesomelic dysplasia-3", "ACROMESOMELIC DYSPLASIA 3", "acromesomelic dysplasia 3", "Demirhan-type acromesomelic dysplasia", "ACROMESOMELIC DYSPLASIA, DEMIRHAN TYPE", "acromesomelic dysplasia, Demirhan type", "chondrodysplasia acromesomelic with genital anomalies", "Chondrodysplasia, acromesomelic, with genital anomalies", "CHONDRODYSPLASIA, ACROMESOMELIC, WITH OR WITHOUT GENITAL ANOMALIES", "chondrodysplasia, acromesomelic, with or without genital anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acromesomelic dysplasia 3", "shortest_name_length": 4}
{"curie": "UMLS:C4528620", "names": ["Stage III Vulvar Cancer", "Stage III Vulvar Cancer AJCC v8", "Stage III Vulvar Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Vulvar Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "UMLS:C5670125", "names": ["Refractory Gastrointestinal Stromal Tumor", "Refractory Malignant Gastrointestinal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Malignant Gastrointestinal Stromal Tumor", "shortest_name_length": 41}
{"curie": "UMLS:C5419184", "names": ["Advanced Cutaneous Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Cutaneous Melanoma", "shortest_name_length": 27}
{"curie": "UMLS:C5447400", "names": ["Locally Advanced Unresectable Primary Central Chondrosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Unresectable Primary Central Chondrosarcoma", "shortest_name_length": 60}
{"curie": "MONDO:0004075", "names": ["Infiltrative lipoma", "Infiltrating Lipoma", "infiltrating lipoma", "Infiltrating lipoma", "infiltrating lipomas", "infiltrating; lipoma", "lipoma; infiltrating", "Intramuscular lipoma", "Intramuscular Lipoma", "intramuscular lipoma", "intramuscular; lipoma", "lipoma; intramuscular", "Infiltrating lipoma (morphologic abnormality)", "intramuscular lipoma (morphologic abnormality)", "Intramuscular lipoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infiltrating lipoma", "shortest_name_length": 19}
{"curie": "UMLS:C0521797", "names": ["Ectopic aldosterone secretion", "Ectopic Aldosterone Secretion", "Ectopic Aldosterone Secretion Syndrome", "Ectopic aldosterone secretion (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ectopic aldosterone secretion", "shortest_name_length": 29}
{"curie": "UMLS:C0339825", "names": ["Nasal Folliculitis", "vestibulitis; nose", "nasal vestibulitis", "NASAL VESTIBULITIS", "Nasal Vestibulitis", "nose; vestibulitis", "Vestibulitis;nasal", "Nasal vestibulitis", "Vestibulitis, nasal", "Nasal vestibulitis NOS", "Nasal vestibulitis, NOS", "Nasal vestibulitis (disorder)", "nasal vestibulitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasal vestibulitis", "shortest_name_length": 18}
{"curie": "UMLS:C4683149", "names": ["Stage IIA Posterior Uveal Melanoma AJCC v8", "Stage IIA Choroidal and Ciliary Body Melanoma", "Stage IIA Choroidal and Ciliary Body Melanoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Choroidal and Ciliary Body Melanoma AJCC v8", "shortest_name_length": 42}
{"curie": "MONDO:0008768", "names": ["CLN6B", "CLN4A", "CLN4A disease", "Kuf's disease type A", "neuronal ceroid lipofuscinosis 6B", "neuronal ceroid lipofuscinosis 4A", "Kuf's disease, autosomal recessive", "CLN6 neuronal ceroid lipofuscinosis", "neuronal ceroid lipofuscinosis type 4A", "adult neuronal ceroid lipofuscinosis 4A", "CEROID LIPOFUSCINOSIS, NEURONAL, 6B (KUFS TYPE)", "ceroid lipofuscinosis, neuronal, 6B (Kufs type)", "autosomal recessive neuronal ceroid lipofuscinosis 4A", "ceroid lipofuscinosis, neuronal, 4A, autosomal recessive", "neuronal ceroid lipofuscinosis caused by mutation in CLN6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ceroid lipofuscinosis, neuronal, 6B (Kufs type)", "shortest_name_length": 5}
{"curie": "MONDO:0009973", "names": ["RD", "aleukocytosis", "ALEUKOCYTOSIS", "Aleukocytosis", "AK2 deficiency", "DeVaal disease", "De Vaal disease", "DE VAAL DISEASE", "De Vaal Disease", "CONGENITAL ALEUKIA", "Congenital aleukia", "congenital Aleukia", "reticular Dysgenesia", "Reticular dysgenesis", "RETICULAR DYSGENESIA", "SCID with leukopenia", "Reticular dysgenesia", "Reticular Dysgenesis", "reticular dysgenesis", "RETICULAR DYSGENESIS", "dysgenesis; reticular", "reticular; dysgenesis", "congenital aleukocytosis", "Congenital aleukocytosis", "Reticular dysgenesis (disorder)", "IMMUNOERYTHROMYELOID HYPOPLASIA", "Immunoerythromyeloid hypoplasia", "Immunoerythromyeloid Hypoplasia", "generalized hematopoietic hypoplasia", "Generalized hematopoietic hypoplasia", "HEMATOPOIETIC HYPOPLASIA, GENERALIZED", "Generalised haematopoietic hypoplasia", "Hematopoietic Hypoplasia, Generalized", "hematopoietic hypoplasia, generalized", "Severe combined immunodeficiency with leukopenia", "SEVERE COMBINED IMMUNODEFICIENCY WITH LEUKOPENIA", "severe combined immunodeficiency with leukopenia", "Severe combined immunodeficiency, neutropenia and thrombocytopenia", "severe combined reticular immunodeficiency with reticular dysgenesis", "Severe combined immunodeficiency, neutropaenia and thrombocytopaenia", "SCID - Severe combined immunodeficiency, neutropenia and thrombocytopenia", "SCID - Severe combined immunodeficiency, neutropaenia and thrombocytopaenia", "severe combined reticular immunodeficiency with reticular dysgenesis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "reticular dysgenesis", "shortest_name_length": 2}
{"curie": "MONDO:0024647", "names": ["calculus", "Urolithiases", "UROLITHIASIS", "Urolithiasis", "urolithiasis", "kidney stone", "Urinary stone", "Urinary Stones", "urinary stones", "Urinary calculus", "Urolithiasis, NOS", "Urinary Lithiasis", "Lithiasis, Urinary", "Urolithiasis (N20-N23)", "Urolithiasis (disorder)", "Urolith in urinary system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urolithiasis", "shortest_name_length": 8}
{"curie": "MONDO:0600018", "names": ["FGFR2 acinar dysplasia", "FGFR2 related acinar dysplasia", "acinar dysplasia caused by mutation in FGFR2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acinar dysplasia caused by mutation in FGFR2", "shortest_name_length": 22}
{"curie": "UMLS:C0399373", "names": ["Amelogenesis imperfecta, hypomaturation hypoplasia type with taurodontism", "Amelogenesis imperfecta, hypomaturation hypoplasia type with taurodontism (disorder)", "Amelogenesis imperfecta - hypomaturation - autosomal dominant - hypoplastic with taurodontism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Amelogenesis imperfecta, hypomaturation hypoplasia type with taurodontism", "shortest_name_length": 73}
{"curie": "MONDO:0001594", "names": ["Capped hock", "capped hock", "Albert disease", "ALBERT DISEASE", "achillobursitis", "alberts disease", "Achillobursitis", "Haglund's disease", "albert's syndrome", "ACHILLES BURSITIS", "Achilles bursitis", "Albert's syndrome", "achilles bursitis", "Haglund deformity", "haglund's disease", "Swediaur's disease", "Calcaneal bursitis", "Haglund's deformity", "bursitis; calcaneal", "TENOSITIS, ACHILLES", "tendonitis achilles", "Swediauer's disease", "calcaneal; bursitis", "achilles tendonitis", "haglund's deformity", "Calcaneal osteochondritis", "CALCANEAL BURSITIS, SUPERFICIAL", "Inflammation of calcaneal bursa", "Achilles bursitis or tendinitis", "Bursitis of calcaneal tendon bursa", "Bursitis of calcaneal tendon bursa (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Achilles bursitis", "shortest_name_length": 11}
{"curie": "UMLS:C0277631", "names": ["strangulation", "Strangulation", "Death by strangulation", "Death by strangulation (event)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Death by strangulation", "shortest_name_length": 13}
{"curie": "MONDO:0005502", "names": ["DF", "DENGUE", "Dengue", "dengue", "DUENGERO", "dandy fever", "Aden; fever", "fever; Aden", "Dengue Fever", "FEVER, DANDY", "fever; dandy", "dengue fever", "dandy; fever", "Dengue fever", "Fever, Dengue", "fever; dengue", "dengue; fever", "classic dengue", "dengue disease", "Breakbone fever", "Breakbone Fever", "breakbone fever", "fever; breakbone", "Break-bone Fever", "Fever, Breakbone", "Break-Bone Fever", "Classical Dengue", "breakbone; fever", "FEVER, BREAKBONE", "classical dengue", "Break-bone fever", "break bone fever", "Break Bone Fever", "FEVER, BREAK BONE", "Classical Dengues", "Fever, Break-Bone", "Dengue, Classical", "Dengue (disorder)", "hemorrhagic dengue", "Classical Dengue Fever", "Thai hemorrhagic fever", "Dengue virus infection", "Dengue Fever, Classical", "Classical Dengue Fevers", "Dengue fever (diagnosis)", "Dengue virus reinfection", "Singapore hemorrhagic fever", "Dengue fever virus infection", "Philippine hemorrhagic fever", "Dengue fever virus reinfection", "Dengue virus infectious disease", "Dengue fever [classical dengue]", "Dengue virus disease or disorder", "Dengue virus caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dengue disease", "shortest_name_length": 2}
{"curie": "MONDO:0018126", "names": ["PMED", "progressive myoclonus epilepsy with dystonia", "Progressive myoclonic epilepsy with dystonia", "Progressive myoclonus epilepsy with dystonia", "progressive myoclonic epilepsy with dystonia", "progressive familial myoclonic epilepsy with dystonia", "Progressive myoclonic epilepsy with dystonia (disorder)", "Progressive myoclonic epilepsy with dystonia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive myoclonic epilepsy with dystonia", "shortest_name_length": 4}
{"curie": "UMLS:C5669690", "names": ["Advanced Extrahepatic Bile Duct Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Extrahepatic Bile Duct Carcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0008793", "names": ["DIVRY-VAN BOGAERT SYNDROME", "Divry-Van Bogaert syndrome", "Angiomatosis, diffuse corticomeningeal, of Divry and Van Bogaert", "ANGIOMATOSIS, DIFFUSE CORTICOMENINGEAL, OF DIVRY AND VAN BOGAERT", "angiomatosis, diffuse Corticomeningeal, of Divry and van Bogaert", "Corticomeningeal angiomatosis, myelination of the white substance of the centrum ovale, hemianopsia and marbled skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angiomatosis, diffuse Corticomeningeal, of Divry and van Bogaert", "shortest_name_length": 26}
{"curie": "UMLS:C0334293", "names": ["Adenocarcinoma in adenomatous polyposis coli", "Adenocarcinoma in Adenomatous Polyposis Coli", "polyposis coli; adenocarcinoma, adenomatous (in)", "Adenocarcinoma in adenomatous polyposis coli (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma in adenomatous polyposis coli", "shortest_name_length": 44}
{"curie": "MONDO:0020442", "names": ["left SVC persisting to left-sided atrium", "Left superior vena cava persisting to left atrium", "left superior vena cava persisting to left-sided atrium", "left superior caval vein persisting to left-sided atrium", "Left superior caval vein persisting to left sided atrium", "Left superior caval vein (SVC) persisting to left sided atrium", "Left superior caval vein persisting to left sided atrium (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "left superior vena cava persisting to left-sided atrium", "shortest_name_length": 40}
{"curie": "MONDO:0006834", "names": ["cancer lip", "lip cancer", "Lip Cancer", "Cancer, Lip", "Lip Cancers", "cancer lips", "lip cancers", "Cancers, Lip", "Lips--Cancer", "cancer of lip", "Cancer of lip", "of lip cancer", "Lip Neoplasms", "Cancer of Lip", "cancer of the lip", "Cancer of the Lip", "CA - Cancer of lip", "Malignant Lip Tumor", "malignant Lip tumor", "Malignant lip cancer", "malignant tumor of lip", "malignant Lip neoplasm", "malignant lip neoplasm", "malignant tumor of Lip", "Malignant Lip Neoplasm", "lip neoplasm malignant", "Malignant lip neoplasm", "Malignant Tumor of Lip", "Malignant tumor of lip", "Malignant tumour of lip", "malignant tumour of lip", "malignant neoplasm of Lip", "Malignant Neoplasm of Lip", "malignant neoplasm of lip", "Malignant neoplasm of lip", "malignant tumor of the Lip", "Malignant Tumor of the Lip", "Malignant Neoplasm of the Lip", "malignant neoplasm of the Lip", "Malignant neoplasm of lip, NOS", "Malignant tumor of mucosa of lip", "malignant tumor of labial mucosa", "Malignant tumor of labial mucosa", "Malignant tumour of mucosa of lip", "Malignant tumour of labial mucosa", "Malignant tumor of lip (disorder)", "malignant neoplasm of lip, external", "malignant neoplasm of labial mucosa", "Malignant tumor of commissure of lip", "Malignant tumor of labial commissure", "malignant tumor of commissure of lip", "malignant neoplasm of lip (diagnosis)", "malignant tumour of labial commissure", "Malignant tumor of oral aspect of lip", "Malignant tumour of commissure of lip", "Malignant tumour of labial commissure", "Malignant tumor of inner aspect of lip", "Malignant tumour of oral aspect of lip", "Malignant neoplasm of lip, unspecified", "malignant neoplasm of lip, unspecified", "malignant tumor of lower labial mucosa", "Malignant neoplasm of lip, oral aspect", "malignant neoplasm of lip, inner aspect", "Malignant neoplasm of lip, inner aspect", "Malignant tumour of inner aspect of lip", "Malignant tumor of buccal aspect of lip", "malignant neoplasm of labial commissure", "malignant neoplasm of commissure of lip", "malignant neoplasm of lower lip, mucosa", "Malignant neoplasm of commissure of lip", "lip neoplasm malignant of labial mucosa", "Malignant tumour of buccal aspect of lip", "Malignant neoplasm of other sites of lip", "malignant neoplasm of other sites of lip", "lip neoplasm malignant labial commissure", "Malignant tumor of labial mucosa (disorder)", "malignant neoplasm of lip, vermilion border", "malignant neoplasm of lower lip, oral aspect", "malignant neoplasm of lower lip, inner aspect", "malignant neoplasm of vermilion border of lip", "malignant neoplasm of lower lip, buccal aspect", "malignant neoplasm of labial commissure of lip", "Malignant neoplasm of labial commissure of lip", "malignant neoplasm of labial mucosa (diagnosis)", "Malignant tumor of commissure of lip (disorder)", "malignant neoplasm of commissure of lip (diagnosis)", "malignant neoplasm of lip, unspecified, inner aspect", "Malignant neoplasm of lip, unspecified, inner aspect", "Malignant neoplasm of buccal aspect of lip, unspecified", "malignant neoplasm of lip, unspecified, vermilion border", "malignant neoplasm of external Lip, not specified as upper or lower", "Malignant neoplasm of oral aspect of lip, not specified whether upper or lower", "malignant neoplasm of oral aspect of lip, not specified whether upper or lower", "Malignant neoplasm of buccal aspect of lip, not specified whether upper or lower"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lip cancer", "shortest_name_length": 10}
{"curie": "MONDO:0006306", "names": ["ductal and lobular carcinoma", "Lobular and ductal carcinoma", "Ductal and Lobular Carcinoma", "Intraductal and lobular carcinoma", "Mixed Lobular and Ductal Carcinoma", "Mixed Ductal and Lobular Carcinoma", "mixed lobular and ductal carcinoma", "Mixed ductal lobular breast carcinoma", "LCIS and Infiltrating Ductal Carcinoma", "Infiltrating duct and lobular carcinoma", "breast mixed ductal and lobular carcinoma", "Mixed Lobular and Ductal Breast Carcinoma", "mixed ductal and lobular breast carcinoma", "Mixed Ductal and Lobular Breast Carcinoma", "Breast Mixed Ductal and Lobular Carcinoma", "mixed lobular and ductal breast carcinoma", "[M] Infiltrating duct and lobular carcinoma", "Mixed Ductal and Lobular Carcinoma of Breast", "Mixed ductal and lobular carcinoma of breast", "mixed ductal and lobular carcinoma of breast", "Mixed Lobular and Ductal Carcinoma of Breast", "mixed lobular and ductal carcinoma of breast", "Invasive Ductal and Lobular Carcinoma In Situ", "Infiltrating duct and lobular carcinoma in situ", "Mixed Lobular and Ductal Carcinoma of the Breast", "mixed ductal and lobular carcinoma of the breast", "Mixed Ductal and Lobular Carcinoma of the Breast", "mixed lobular and ductal carcinoma of the breast", "Infiltrating Ductal and Lobular Carcinoma in situ", "Carcinoma of breast with ductal and lobular features", "Lobular Carcinoma in situ and Invasive Ductal Carcinoma", "Infiltrating lobular carcinoma and ductal carcinoma in situ", "Lobular Carcinoma in situ and Infiltrating Ductal Carcinoma", "carcinoma; infiltrating duct with lobular ca, unspecified site", "Invasive Breast Ductal Carcinoma and Lobular Carcinoma In Situ", "Carcinoma of breast with ductal and lobular features (disorder)", "Carcinoma of breast with ductal and lobular features (diagnosis)", "Infiltrating duct and lobular carcinoma (morphologic abnormality)", "breast neoplasm malignant carcinoma with ductal and lobular features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed lobular and ductal breast carcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0011586", "names": ["OTSC2", "otosclerosis 2", "Otosclerosis 2", "OTOSCLEROSIS 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "otosclerosis 2", "shortest_name_length": 5}
{"curie": "MONDO:0019933", "names": ["acromegaly", "Acromegaly", "ACROMEGALY", "acromegalia", "Acromegalia", "GH increased", "marie disease", "Marie disease", "HGH, INCREASED", "pituitary giant", "Marie's syndrome", "Somatotropin high", "Somatotropin excess", "somatotroph adenoma", "Growth hormone excess", "Acromegaly (disorder)", "Growth Hormone Excess", "GROWTH HORMONE EXCESS", "growth hormone excess", "excess growth hormone", "Somatotropin increased", "acromegaly (diagnosis)", "SOMATOTROPIN, INCREASED", "Somatotrophin increased", "Growth hormone increased", "Increased growth hormone", "increased growth hormone", "GROWTH HORMONE, INCREASED", "STH hypersecretion syndrome", "Eosinophilic adenoma syndrome", "Anterior pituitary adenoma syndrome", "Growth hormone hypersecretion syndrome", "Growth hormone concentrations above normal", "Elevated circulating somatotropin concentration", "Inappropriate GH Secretion Syndrome (Acromegaly)", "Somatotropin Hypersecretion Syndrome (Acromegaly)", "Elevated circulating growth hormone concentration", "Somatotropin Hypersecretion Syndromes (Acromegaly)", "Hypersecretion Syndrome, Somatotropin (Acromegaly)", "Syndrome, Somatotropin Hypersecretion (Acromegaly)", "Hypersecretion Syndromes, Somatotropin (Acromegaly)", "Syndromes, Somatotropin Hypersecretion (Acromegaly)", "Growth hormone concentrations above normal (finding)", "Inappropriate Growth Hormone Secretion Syndrome (Acromegaly)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acromegaly", "shortest_name_length": 10}
{"curie": "UMLS:C4524968", "names": ["stage IIIB small intestine cancer", "Stage IIIB Small Intestinal Adenocarcinoma", "Stage IIIB Small Intestinal Adenocarcinoma AJCC v8", "stage IIIB small intestinal adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Small Intestinal Adenocarcinoma AJCC v8", "shortest_name_length": 33}
{"curie": "MONDO:0015394", "names": ["nasal encephalocele", "Nasal encephalocele", "Encephalocele, nasal", "Nasal encephalocele (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasal encephalocele", "shortest_name_length": 19}
{"curie": "UMLS:C1335716", "names": ["Recurrent Nodular Lymphocyte Predominant Hodgkin Lymphoma", "Relapsed Nodular Lymphocyte Predominant Hodgkin's Disease", "Recurrent Nodular Lymphocyte Predominant Hodgkin's Disease", "Relapsed Nodular Lymphocyte Predominant Hodgkin's Lymphoma", "Recurrent Nodular Lymphocyte Predominant Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Nodular Lymphocyte Predominant Hodgkin Lymphoma", "shortest_name_length": 57}
{"curie": "MONDO:0003379", "names": ["rectum leiomyosarcoma", "rectal leiomyosarcoma", "Rectal Leiomyosarcoma", "Leiomyosarcoma of rectum", "leiomyosarcoma of rectum", "Leiomyosarcoma of Rectum", "leiomyosarcoma of the rectum", "Leiomyosarcoma of the Rectum", "Leiomyosarcoma of rectum (disorder)", "leiomyosarcoma of rectum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rectum leiomyosarcoma", "shortest_name_length": 21}
{"curie": "MONDO:0100134", "names": ["mitochondrial complex I deficiency, mitochondrial type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex I deficiency, mitochondrial type", "shortest_name_length": 54}
{"curie": "MONDO:0019506", "names": ["Obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay syndrome", "obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay syndrome", "Obesity, colitis, hypothyroidism, cardiac hypertrophy, developmental delay syndrome", "Obesity, colitis, hypothyroidism, cardiac hypertrophy, developmental delay syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay syndrome", "shortest_name_length": 79}
{"curie": "MONDO:0020858", "names": ["MC5DN5", "mitochondrial complex v (atp synthase) deficiency", "Mitochondrial Complex 5 (ATP Synthase) Deficiency, ATP5F1D Type", "MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATP5F1D TYPE", "mitochondrial complex 5 (ATP synthase) deficiency nuclear type 5", "mitochondrial complex V (ATP synthase) deficiency nuclear type 5", "MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 5 (ATP synthase) deficiency nuclear type 5", "shortest_name_length": 6}
{"curie": "MONDO:0036042", "names": ["KAT6B-related disorder", "KAT6B-related multiple congenital anomalies syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "KAT6B-related multiple congenital anomalies syndrome", "shortest_name_length": 22}
{"curie": "OMIM:612797", "names": ["HDLCQ12", "HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 7}
{"curie": "MONDO:0017217", "names": ["visceral calciphylaxis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "visceral calciphylaxis", "shortest_name_length": 22}
{"curie": "MONDO:0007774", "names": ["HRX", "hyperreflexia", "reflex abnormal", "Abnormal;reflex", "Abnormal reflex", "Abnormal Reflex", "abnormal reflex", "reflex; abnormal", "abnormal; reflex", "Reflex, Abnormal", "Abnormal Reflexes", "reflexes abnormal", "REFLEXES ABNORMAL", "abnormal reflexes", "Reflexes abnormal", "Abnormal reflexes", "Reflexes, Abnormal", "Abnormal reflex, NOS", "hyperreflexia (disease)", "Abnormal reflex (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperreflexia", "shortest_name_length": 3}
{"curie": "MONDO:0003840", "names": ["epicardium lipoma", "epicardial lipoma", "Epicardial Lipoma", "Lipoma of Epicardium", "lipoma of epicardium", "lipoma of the epicardium", "Lipoma of the Epicardium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epicardium lipoma", "shortest_name_length": 17}
{"curie": "UMLS:C0752307", "names": ["Cerebral Ischemia Anoxia", "Cerebral Anoxia-Ischemia", "Cerebral Anoxia Ischemia", "Cerebral Ischemia-Anoxia", "Ischemia-Anoxia, Cerebral", "Anoxia-Ischemia, Cerebral", "Cerebral Anoxia-Ischemias", "Anoxia Ischemia, Cerebral", "Cerebral Ischemia-Anoxias", "Ischemia Anoxia, Cerebral", "Anoxia-Ischemias, Cerebral", "Ischemia-Anoxias, Cerebral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anoxia-Ischemia, Cerebral", "shortest_name_length": 24}
{"curie": "UMLS:C1334305", "names": ["Parameniscal Cyst", "Periarticular Myxoma", "Juxtaarticular Myxoma", "Juxta-Articular Myxoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Juxta-Articular Myxoma", "shortest_name_length": 17}
{"curie": "MONDO:0012290", "names": ["CEDNIK", "CEDNIK SYNDROME", "CEDNIK syndrome", "cerebral dysgenesis, neuropathy, ichthyosis and keratoderma syndrome", "CEDNIK (cerebral dysgenesis, neuropathy, ichthyosis, keratoderma) syndrome", "cerebral dysgenesis-neuropathy-ichthyosis-palmoplantar keratoderma syndrome", "Cerebral dysgenesis-neuropathy-ichthyosis-palmoplantar keratoderma syndrome", "Cerebral dysgenesis, neuropathy, ichthyosis, palmoplantar keratoderma syndrome", "cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome", "CEREBRAL DYSGENESIS, NEUROPATHY, ICHTHYOSIS, AND PALMOPLANTAR KERATODERMA SYNDROME", "Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome", "Cerebral dysgenesis, neuropathy, ichthyosis, palmoplantar keratoderma syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CEDNIK syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C5230949", "names": ["Melanocytic Matricoma", "Melanocytic matricoma", "Melanocytic matricoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Melanocytic matricoma", "shortest_name_length": 21}
{"curie": "MONDO:0006427", "names": ["Spindle cell melanoma", "spindle cell melanoma", "Spindle Cell Melanoma", "desmoplastic melanoma", "Spindle cell melanoma NOS", "Spindle cell melanoma, NOS", "spitzoid malignant melanoma", "Spitzoid malignant melanoma", "spindle cell malignant melanoma", "Spindle cell malignant melanoma", "Spindle Cell Malignant Melanoma", "Malignant Spindle Cell Melanoma", "malignant spindle cell melanoma", "malignant neoplasm melanoma spindle cell", "Spindle cell malignant melanoma (disorder)", "Spindle cell malignant melanoma (diagnosis)", "Spindle cell melanoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spindle cell melanoma", "shortest_name_length": 21}
{"curie": "UMLS:C0265451", "names": ["monosomy 13q", "13q- syndrome", "orbeli syndrome", "Orbeli syndrome", "del(13q) syndrome", "Orbeli's syndrome", "13q minus syndrome", "partial monosomy 13q", "Deletion 13q syndrome", "13q deletion syndrome", "Monosomy 13q Syndrome", "13q Deletion Syndrome", "deletion 13q syndrome", "Monosomy 13q syndrome", "chromosome 13q monosomy", "13q partial monosomy syndrome", "partial monosomy 13q syndrome", "Chromosome 13q deletion syndrome", "chromosome 13q deletion syndrome", "Partial deletion of chromosome 13q", "Partial monosomy of chromosome 13q", "13q partial monosomy syndrome (disorder)", "13q partial monosomy syndrome (diagnosis)", "Partial monosomy of the long arm of chromosome 13", "Partial deletion of the long arm of chromosome 13"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chromosome 13q deletion syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0001221", "names": ["varix esophagus", "Esophageal Varix", "esophageal varix", "ESOPHAGEAL VARIX", "Esophageal varix", "ESOPHAGUS, VARIX", "esophageal varice", "Varix, Esophageal", "Oesophageal varix", "varices; esophagus", "esophageal varices", "Varices esophageal", "Esophageal Varices", "Esophageal varices", "ESOPHAGEAL VARICES", "esophagus; varices", "VARICES ESOPHAGEAL", "varices esophageal", "oesophageal varices", "Varices, Esophageal", "Oesophageal varices", "Varices;oesophageal", "Varices oesophageal", "OESOPHAGEAL VARICES", "Esophageal varices NOS", "OV - Esophageal varices", "Oesophageal varices NOS", "Esophageal varices, NOS", "esophagus varicose veins", "Oesophageal varices, NOS", "varicose veins esophagus", "OV - Oesophageal varices", "Varicose veins;oesophagus", "esophagus varicose disease", "gastric esophageal varices", "esophageal gastric varices", "Enlarged vein in esophagus", "Enlarged vein in oesophagus", "Bleeding esophageal varices", "bleeding esophageal varices", "Bleeding oesophageal varices", "bleeding oesophageal varices", "Esophageal varices (disorder)", "varicose disease of esophagus", "esophageal varices (diagnosis)", "Esophageal and Gastric Varices", "Esophageal varices (diagnosis)", "varicose veins on the esophagus", "varicose veins on the oesophagus", "esophageal varices with bleeding", "esophageal varices without bleeding", "esophageal varices without mention of bleeding", "esophageal varices with bleeding in disease EC", "esophageal varices in diseases classified elsewhere", "Esophageal varices in diseases classified elsewhere", "Oesophageal varices in diseases classified elsewhere", "bleeding esophageal varices in diseases classified elsewhere", "esophageal varices in diseases classified elsewhere (diagnosis)", "esophageal varices in disease classified elsewhere with bleeding", "esophageal varices in disease classified elsewhere, with bleeding", "Esophageal varices in diseases classified elsewhere, with bleeding", "Oesophageal varices in diseases classified elsewhere, with bleeding", "esophageal varices in disease classified elsewhere with bleeding (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophageal varices", "shortest_name_length": 15}
{"curie": "MONDO:0012700", "names": ["dRTA with anemia", "distal renal tubular acidosis with anemia", "renal tubular acidosis, distal, with hemolytic anemia", "distal renal tubular acidosis 4 with hemolytic anemia", "Renal Tubular Acidosis, Distal, With Hemolytic Anemia", "RTA, Distal, Autosomal Recessive, With Hemolytic Anemia", "RTA, distal, autosomal recessive, with hemolytic Anemia", "renal tubular acidosis, distal, 4, with hemolytic anemia", "Renal Tubular Acidosis, Distal, With Normal Red Cell Morphology", "renal tubular acidosis, distal, with normal Red cell morphology", "RENAL TUBULAR ACIDOSIS, DISTAL, WITH NORMAL RED CELL MORPHOLOGY", "RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal tubular acidosis, distal, 4, with hemolytic anemia", "shortest_name_length": 16}
{"curie": "MONDO:0008176", "names": ["PDB3", "PAGET DISEASE OF BONE 3", "Paget disease of bone-3", "Paget disease of bone 3", "Paget's disease of bone 3", "Paget disease of bone type 3", "familial Paget disease of bone", "Paget disease of bone, familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paget disease of bone 3", "shortest_name_length": 4}
{"curie": "MONDO:0021478", "names": ["Benign tumor of epipharynx", "Benign Tumor of Nasopharynx", "Benign Nasopharyngeal Tumor", "benign tumor of nasopharynx", "nasopharynx benign neoplasm", "Benign tumor of nasopharynx", "Benign tumour of epipharynx", "benign nasopharyngeal tumor", "Benign tumour of nasopharynx", "Nasopharyngeal neoplasm benign", "benign nasopharyngeal neoplasm", "Benign Neoplasm of Nasopharynx", "benign neoplasm of nasopharynx", "Benign Nasopharyngeal Neoplasm", "Benign nasopharyngeal neoplasm", "Benign neoplasm of nasopharynx", "benign tumor of the nasopharynx", "Benign tumor of postnasal space", "nasopharyngeal neoplasm, benign", "Benign Tumor of the Nasopharynx", "Nasopharyngeal Neoplasm, Benign", "Benign tumour of postnasal space", "Benign Neoplasm of the Nasopharynx", "benign neoplasm of the nasopharynx", "Benign neoplasm of nasopharynx, NOS", "Benign tumor of nasopharynx (disorder)", "benign neoplasm of nasopharynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of nasopharynx", "shortest_name_length": 26}
{"curie": "UMLS:C1519864", "names": ["Uterine Corpus STUMP", "Borderline Uterine Corpus Smooth Muscle Neoplasm", "Uterine Corpus Smooth Muscle Tumor of Uncertain Malignant Potential", "Uterine Corpus Smooth Muscle Neoplasm of Uncertain Malignant Potential"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Corpus Smooth Muscle Tumor of Uncertain Malignant Potential", "shortest_name_length": 20}
{"curie": "MONDO:0016504", "names": ["PUAH", "primary unilateral adrenal hyperplasia", "Primary unilateral adrenal hyperplasia", "Primary unilateral adrenal hyperplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary unilateral adrenal hyperplasia", "shortest_name_length": 4}
{"curie": "MONDO:0011432", "names": ["BMRS type V", "BMRS, Verloes type", "blepharophimosis-intellectual disability syndrome type V", "blepharophimosis-mental retardation syndrome, Verloes type", "BLEPHAROPHIMOSIS-MENTAL RETARDATION SYNDROME, VERLOES TYPE", "blepharophimosis-intellectual disability syndrome, Verloes type", "blepharophimosis - intellectual disability syndrome, Verloes type", "Blepharophimosis with Facial and Genital Anomalies and Mental Retardation", "BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION", "blepharophimosis with facial and genital anomalies and mental retardation", "blepharophimosis with facial and genital anomalies and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blepharophimosis - intellectual disability syndrome, Verloes type", "shortest_name_length": 11}
{"curie": "MONDO:0022007", "names": ["WATER INTOX", "Overhydration", "Hyperhydration", "WATER INTOXICATION", "water intoxication", "Water Intoxication", "Water intoxication", "intoxication; water", "water; intoxication", "Water intoxication syndrome", "water intoxication syndrome", "Water intoxication syndrome (disorder)", "water intoxication syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "water intoxication", "shortest_name_length": 11}
{"curie": "MONDO:0009805", "names": ["OI9", "OI 9", "OI type IX", "OI, type 9", "OI, TYPE IX", "OI, Type IX", "PPIB osteogenesis imperfecta", "OI9 Osteogenesis Imperfecta 9", "osteogenesis imperfecta type 9", "osteogenesis imperfecta type IX", "osteogenesis imperfecta, type 9", "Osteogenesis Imperfecta, Type IX", "osteogenesis imperfecta, type IX", "OSTEOGENESIS IMPERFECTA, TYPE IX", "OI, type 9 Osteogenesis Imperfecta, type 9", "OI, type IX Osteogenesis Imperfecta, type IX", "osteogenesis imperfecta caused by mutation in PPIB", "osteogenesis imperfecta sillence type II/III without abnormality of type I collagen", "Osteogenesis Imperfecta, Sillence Type II-III, Without Abnormality of Type I Collagen"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteogenesis imperfecta type 9", "shortest_name_length": 3}
{"curie": "MONDO:0015047", "names": ["amelogenesis imperfecta type 1", "hypoplastic amelogenesis imperfecta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amelogenesis imperfecta type 1", "shortest_name_length": 30}
{"curie": "MONDO:0012009", "names": ["CHDS2", "Chds2", "CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 2", "coronary heart disease, susceptibility to, 2", "coronary heart disease, susceptibility to, type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coronary heart disease, susceptibility to, 2", "shortest_name_length": 5}
{"curie": "MONDO:0007844", "names": ["HH2", "KAL2", "Kallmann Syndrome 2", "Kallmann syndrome 2", "KALLMANN SYNDROME 2", "FGFR1 hypogonadotropic hypogonadism", "Autosomal Dominant Form of Kallmann Syndrome", "HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA", "hypogonadotropic hypogonadism 2 with or without anosmia", "hypogonadotropic hypogonadism caused by mutation in FGFR1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadotropic hypogonadism 2 with or without anosmia", "shortest_name_length": 3}
{"curie": "MONDO:0017590", "names": ["AMPCA", "Ampulloma", "ampullary cancer", "ampullary carcinoma", "Ampullary Carcinoma", "Ampullary carcinoma", "ampulla of vater cancer", "ampulla of Vater cancer", "Ampulla of Vater Cancer", "AMPULLA VATER CARCINOMA", "Carcinoma ampulla of Vater", "Ampulla of Vater carcinoma", "ampulla of Vater carcinoma", "Ampulla of Vater Carcinoma", "carcinoma of ampulla of vater", "CARCINOMA OF AMPULLA OF VATER", "Carcinoma of ampulla of Vater", "AMPULLA VATER CANCER, CARCINOMA", "carcinoma of the ampulla of vater", "Carcinoma of the ampulla of Vater", "hepatopancreatic ampulla carcinoma", "carcinoma of hepatopancreatic ampulla", "Carcinoma of ampulla of Vater (disorder)", "Carcinoma of ampulla of Vater (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma of the ampulla of vater", "shortest_name_length": 5}
{"curie": "MONDO:0014806", "names": ["SMABF1", "SMA1 with congenital bone fractures", "SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1", "spinal muscular atrophy with congenital bone fractures 1", "spinal muscular atrophy with congenital bone fractures type 1", "spinal muscular atrophy type 1 with congenital bone fractures", "Spinal Muscular Atrophy, Type I, with Congenital Bone Fractures", "spinal muscular atrophy, type I, with congenital bone fractures", "SPINAL MUSCULAR ATROPHY, TYPE I, WITH CONGENITAL BONE FRACTURES", "TRIP4 prenatal-onset spinal muscular atrophy with congenital bone fractures", "prenatal-onset spinal muscular atrophy with congenital bone fractures caused by mutation in TRIP4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal muscular atrophy with congenital bone fractures 1", "shortest_name_length": 6}
{"curie": "UMLS:C5670657", "names": ["CNS CIC-Rearranged Sarcoma", "Central Nervous System CIC-Rearranged Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System CIC-Rearranged Sarcoma", "shortest_name_length": 26}
{"curie": "MONDO:0020568", "names": ["Dermal myiasis", "Myiasis, dermal", "cutaneous myiasis", "Cutaneous myiasis", "skin; myiasis (etiology)", "myiasis; skin (etiology)", "dermal; myiasis (etiology)", "myiasis; dermal (etiology)", "skin; myiasis (manifestation)", "myiasis; cutaneous (etiology)", "cutaneous; myiasis (etiology)", "myiasis; skin (manifestation)", "dermal; myiasis (manifestation)", "myiasis; dermal (manifestation)", "cutaneous; myiasis (manifestation)", "myiasis; cutaneous (manifestation)", "Infestation of skin caused by fly larvae", "Infestation of skin caused by fly larvae (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous myiasis", "shortest_name_length": 14}
{"curie": "MONDO:0010633", "names": ["IHG", "ASGD3", "iris hypoplasia and glaucoma", "Iris hypoplasia and glaucoma", "iris hypoplasia with glaucoma", "ANTERIOR SEGMENT DYSGENESIS 3", "Iris Hypoplasia with Glaucoma", "IRIS HYPOPLASIA WITH GLAUCOMA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "iris hypoplasia with glaucoma", "shortest_name_length": 3}
{"curie": "UMLS:C0155840", "names": ["Nasal turbinate hypertrophy", "nasal turbinate hypertrophied", "hypertrophied nasal turbinate", "nasal; hypertrophy, turbinate", "hypertrophy; nasal, turbinate", "hypertrophy of nasal turbinates", "Hypertrophy of nasal turbinates", "hypertrophied nasal turbinate (diagnosis)", "Hypertrophy of nasal turbinates (disorder)", "hypertrophied nasal turbinate (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypertrophy of nasal turbinates", "shortest_name_length": 27}
{"curie": "MONDO:0003925", "names": ["Ethmoid Sinus Inverted Papilloma", "ethmoid sinus inverted papilloma", "inverted papilloma of ethmoid sinus", "Inverted Papilloma of Ethmoid Sinus", "Inverted papilloma of the ethmoid sinus", "Inverted Papilloma of the Ethmoid Sinus", "inverted papilloma of the ethmoid sinus", "Ethmoid Sinus Inverted Schneiderian Papilloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ethmoid sinus inverted papilloma", "shortest_name_length": 32}
{"curie": "UMLS:C5420537", "names": ["Primary Middle Ear Meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Middle Ear Meningioma", "shortest_name_length": 29}
{"curie": "MONDO:0014440", "names": ["BBS12", "BARDET-BIEDL SYNDROME 12", "Bardet-Biedl syndrome 12", "Bardet-Biedl Syndrome 12", "BBS12 Bardet-Biedl syndrome", "Bardet-Biedl syndrome type 12", "Bardet-Biedl syndrome caused by mutation in BBS12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bardet-Biedl syndrome 12", "shortest_name_length": 5}
{"curie": "UMLS:C1336250", "names": ["Stage III Immature Testicular Teratoma", "Stage III Immature Testicular Teratoma AJCC v6", "Stage III Immature Testicular Teratoma AJCC v7", "Stage III Immature Testicular Teratoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Immature Testicular Teratoma AJCC v6 and v7", "shortest_name_length": 38}
{"curie": "MONDO:0009134", "names": ["Cda 2", "CDAN2", "CDA II", "HEMPAS", "SEC23B-CDG", "CDA type 2", "CDA type II", "CDA, TYPE II", "H.E.M.P.A.S.", "hempas anemia", "HEMPAS Anemia", "HEMPAS Anemias", "Dyserythropoietic Anemia, HEMPAS Type", "dyserythropoietic Anemia, hempas type", "DYSERYTHROPOIETIC ANEMIA, HEMPAS TYPE", "Congenital dyserythropoietic anemia type 2", "congenital dyserythropoietic anemia type 2", "Congenital dyserythropoietic anemia type II", "congenital dyserythropoietic anemia type II", "Congenital dyserythropoietic anaemia type 2", "Dyserythropoietic Anemia, Congenital Type 2", "Congenital Dyserythropoietic Anemia Type II", "congenital dyserythropoietic anaemia type II", "Congenital dyserythropoietic anaemia type II", "anemia, dyserythropoietic, congenital type 2", "Anemia, Dyserythropoietic, Congenital Type 2", "Congenital dyserythropoietic anemia, type II", "anemia, congenital dyserythropoietic, type 2", "dyserythropoietic Anemia, congenital, type 2", "anemia, congenital dyserythropoietic, type II", "Dyserythropoietic Anemia, Congenital, Type II", "Anemia, Congenital Dyserythropoietic, Type II", "Anemia, Dyserythropoietic Congenital, Type II", "ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE II", "DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE II", "Congenital dyserythropoietic anaemia, type II", "dyserythropoietic anemia, congenital, type II", "Anemia, Dyserythropoietic, Congenital, Type II", "Congenital dyserythropoietic anemia, type II (disorder)", "Hereditary erythroblast multinuclearity with positive acid serum test", "Hereditary Erythroblast Multinuclearity with Positive Acidified Serum", "HEREDITARY ERYTHROBLASTIC MULTINUCLEARITY WITH POSITIVE ACIDIFIED-SERUM TEST", "Hereditary Erythroblastic Multinuclearity with Positive Acidified-Serum Test", "hereditary erythroblastic multinuclearity with Positive acidified-serum test", "Hereditary erythrocytic multinuclearity with positive acidified serum syndrome", "HEMPAS - Hereditary erythroblast multinuclearity with positive acid serum test", "hereditary erythroblastic multinuclearity with a positive acidified-serum test (hempas)", "Hereditary erythroblastic multinuclearity with a positive acidified-serum test (hempas)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital dyserythropoietic anemia type 2", "shortest_name_length": 5}
{"curie": "MONDO:0014956", "names": ["CHYTS", "CHITAYAT SYNDROME", "Chitayat syndrome", "Chitayat syndrome; CHYTS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chitayat syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0014494", "names": ["PSORS15", "psoriasis 15", "AP1S3 generalized pustular psoriasis", "susceptibility to pustular psoriasis 15", "psoriasis 15, pustular, susceptibility to", "PSORIASIS 15, PUSTULAR, SUSCEPTIBILITY TO", "generalized pustular psoriasis caused by mutation in AP1S3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "psoriasis 15, pustular, susceptibility to", "shortest_name_length": 7}
{"curie": "MONDO:0021093", "names": ["CED1", "Levin syndrome 1", "Sensenbrenner syndrome", "cranioectodermal dysplasia 1", "cranioectodermal dysplasia type 1", "IFT122 cranioectodermal dysplasia", "cranioectodermal dysplasia caused by mutation in IFT122"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cranioectodermal dysplasia 1", "shortest_name_length": 4}
{"curie": "UMLS:C5205723", "names": ["Oligometastatic Malignant Solid Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oligometastatic Malignant Solid Neoplasm", "shortest_name_length": 40}
{"curie": "MONDO:0006761", "names": ["FMDA", "fibromuscular dysplasia", "Fibromuscular Dysplasia", "ARTERIAL FIBRODYSPLASIA", "Fibromuscular dysplasia", "Dysplasia, fibromuscular", "DYSPLASIA, FIBROMUSCULAR", "Dysplasia, Fibromuscular", "Fibromuscular Dysplasias", "Fibromuscular hyperplasia", "Fibromuscular Hyperplasia", "Hyperplasia, fibromuscular", "fibromuscular; hyperplasia", "hyperplasia; fibromuscular", "FMD - Fibromuscular dysplasia", "Arterial fibromuscular dysplasia", "Arteries Fibromuscular Dysplasia", "arterial fibromuscular dysplasia", "Arteries Fibromuscular Dysplasias", "FIBROMUSCULAR DYSPLASIA, ARTERIAL", "fibromuscular arterial hyperplasia", "Fibromuscular hyperplasia of artery", "Fibromuscular Dysplasia of Arteries", "fibromuscular dysplasia of arteries", "fibromuscular hyperplasia of artery", "FIBROMUSCULAR DYSPLASIA OF ARTERIES", "Fibromuscular dysplasia of wall of artery", "[OBSOLETE] Fibromuscular dysplasia of arteries", "fibromuscular hyperplasia of artery (diagnosis)", "Fibromuscular dysplasia (morphologic abnormality)", "Fibromuscular dysplasia of wall of artery (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibromuscular dysplasia", "shortest_name_length": 4}
{"curie": "MONDO:0030316", "names": ["LMPHM11", "LYMPHATIC MALFORMATION 11", "lymphatic malformation 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphatic malformation 11", "shortest_name_length": 7}
{"curie": "MONDO:0100221", "names": ["IFAP2", "IFAP syndrome 2", "IFAP SYNDROME 2", "ICHTHYOSIS FOLLICULARIS, ATRICHIA, AND PHOTOPHOBIA SYNDROME 2", "ichthyosis follicularis, atrichia, and photophobia syndrome 2", "ichthyosis , follicular, with atrichia and photophobia syndrome 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IFAP syndrome 2", "shortest_name_length": 5}
{"curie": "UMLS:C0877223", "names": ["Intestinal stoma site bleeding", "intestinal stoma site bleeding", "Intestinal Stoma Site Bleeding", "Intestinal Stoma Site Hemorrhage", "intestinal stoma site bleeding (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal Stoma Site Hemorrhage", "shortest_name_length": 30}
{"curie": "UMLS:C4763391", "names": ["Recurrent PVRL", "Recurrent Primary Vitreoretinal Lymphoma", "Recurrent Primary Vitreoretinal Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Primary Vitreoretinal Non-Hodgkin Lymphoma", "shortest_name_length": 14}
{"curie": "MONDO:0010197", "names": ["WHISTLING FACE SYNDROME, RECESSIVE FORM", "whistling face syndrome, recessive form", "Whistling face syndrome, recessive form", "autosomal recessive Whistling face syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "whistling face syndrome, recessive form", "shortest_name_length": 39}
{"curie": "UMLS:C5670687", "names": ["Circumscribed Meningeal Melanocytic Tumor", "Circumscribed Meningeal Melanocytic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Circumscribed Meningeal Melanocytic Neoplasm", "shortest_name_length": 41}
{"curie": "MONDO:0012164", "names": ["Meacham syndrome", "MEACHAM SYNDROME", "Meacham Syndrome", "Meacham syndrome (disorder)", "MEACHAM SYNDROME (disorder)", "Meacham Winn Culler syndrome", "Meacham-Winn-Culler syndrome", "Rhabdomyomatous dysplasia-cardiopathy-genital anomalies syndrome", "Double vagina, cardiac, pulmonary, and other genital malformations with 46,XY karyotype"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meacham syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0003856", "names": ["malignant adult hemangiopericytoma", "Adult Malignant Hemangiopericytoma", "adult malignant hemangiopericytoma", "Malignant Adult Hemangiopericytoma", "malignant hemangiopericytoma, adult", "adult hemangiopericytoma, malignant", "hemangiopericytoma, malignant, adult", "hemangiopericytoma, malignant of adults"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult malignant hemangiopericytoma", "shortest_name_length": 34}
{"curie": "UMLS:C5446564", "names": ["Lacrimal System Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lacrimal System Diffuse Large B-Cell Lymphoma", "shortest_name_length": 45}
{"curie": "UMLS:C5239039", "names": ["Myelodysplastic Syndrome, Unclassifiable, Based on Defining Cytogenetic Abnormality"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myelodysplastic Syndrome, Unclassifiable, Based on Defining Cytogenetic Abnormality", "shortest_name_length": 83}
{"curie": "MONDO:0014072", "names": ["D2L2AD", "D,L-2-HGA", "D,L-2-hydroxyglutaric aciduria", "D,L-2-hydroxyglutaric acidemia", "D,L-2-hydroxyglutaric acidaemia", "combined D,L-2-hydroxyglutaric aciduria", "combined D-2- and L-2-hydroxyglutaric aciduria", "Combined D-2- and L-2-hydroxyglutaric aciduria", "COMBINED D-2- AND L-2-HYDROXYGLUTARIC ACIDURIA", "COMBINED D-2- AND L-2 -HYDROXYGLUTARIC ACIDURIA", "D-2-hydroxyglutaric and L-2-hydroxyglutaric aciduria", "Combined D-2-hydroxyglutaric aciduria and L-2-hydroxyglutaric aciduria", "combined D-2-hydroxyglutaric acidemia and L-2-hydroxyglutaric acidemia", "combined D-2-hydroxyglutaric aciduria and L-2-hydroxyglutaric aciduria", "Combined D-2-hydroxyglutaric acidemia and L-2-hydroxyglutaric acidemia", "Combined D-2-hydroxyglutaric acidaemia and L-2-hydroxyglutaric acidaemia", "Combined D-2-hydroxyglutaric aciduria and L-2-hydroxyglutaric aciduria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "D,L-2-hydroxyglutaric aciduria", "shortest_name_length": 6}
{"curie": "MONDO:0006198", "names": ["endometrium squamous cell carcinoma", "endometrial squamous cell carcinoma", "Endometrial Squamous Cell Carcinoma", "Endometrial squamous cell carcinoma", "squamous cell carcinoma of Endometrium", "Squamous Cell Carcinoma of Endometrium", "squamous cell carcinoma of endometrium", "squamous cell carcinoma of the endometrium", "Squamous Cell Carcinoma of the Endometrium", "Primary squamous cell carcinoma of endometrium", "Primary squamous cell carcinoma of endometrium (disorder)", "Primary squamous cell carcinoma of endometrium (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometrial squamous cell carcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C4553745", "names": ["Stage IIIC Fallopian Tube Cancer", "Stage IIIC Fallopian Tube Cancer AJCC v8", "Stage IIIC Fallopian Tube Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Fallopian Tube Cancer AJCC v8", "shortest_name_length": 32}
{"curie": "UMLS:C3501679", "names": ["Bleeding Disorder due to Defective Thromboxane A2 Receptor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bleeding Disorder due to Defective Thromboxane A2 Receptor", "shortest_name_length": 58}
{"curie": "UMLS:C1334723", "names": ["Brain Metastases, Adult", "Metastasis to the Adult Brain", "Metastatic Tumor to the Adult Brain", "Metastatic Neoplasm to the Adult Brain", "Secondary Malignant Tumor to the Adult Brain", "Secondary Malignant Neoplasm to the Adult Brain", "Metastatic Adult Malignant Neoplasm in the Brain", "Metastatic Malignant Neoplasm in the Adult Brain", "Metastatic Malignant Neoplasm to the Adult Brain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Malignant Neoplasm in the Adult Brain", "shortest_name_length": 23}
{"curie": "UMLS:C4744569", "names": ["Recurrent Blastic Plasmacytoid Dendritic Cell Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Blastic Plasmacytoid Dendritic Cell Neoplasm", "shortest_name_length": 54}
{"curie": "UMLS:C0854918", "names": ["Urethra cancer local", "Urethral cancer local", "Urethra cancer regional", "Urethral cancer regional", "Local Malignant Urethra Tumor", "Local Malignant Urethral Tumor", "Local Malignant Tumor of Urethra", "Regional Malignant Urethra Tumor", "Local Malignant Urethra Neoplasm", "Regional Malignant Urethral Tumor", "Local Malignant Urethral Neoplasm", "Regional Malignant Urethra Neoplasm", "Malignant neoplasm of urethra local", "Local Malignant Neoplasm of Urethra", "Regional Malignant Tumor of Urethra", "Regional Malignant Urethral Neoplasm", "Local Malignant Tumor of the Urethra", "Regional Malignant Neoplasm of Urethra", "Malignant neoplasm of urethra regional", "Regional Malignant Tumor of the Urethra", "Local Malignant Neoplasm of the Urethra", "Regional Malignant Neoplasm of the Urethra"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant neoplasm of urethra local", "shortest_name_length": 20}
{"curie": "UMLS:C3273126", "names": ["Extrahepatic Bile Duct Adenocarcinoma, Biliary Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extrahepatic Bile Duct Adenocarcinoma, Biliary Type", "shortest_name_length": 51}
{"curie": "UMLS:C2347759", "names": ["Grade II Meningioma", "Childhood Grade 2 Meningioma", "grade II childhood meningioma", "childhood grade II meningioma", "Childhood Grade II Meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Grade II Meningioma", "shortest_name_length": 19}
{"curie": "MONDO:0020592", "names": ["disease pharynx", "Pharynx Disease", "PHARYNX DISEASE", "pharynx; disease", "pharynx disorder", "Pharynx Diseases", "Disease, Pharynx", "Pharynx--Diseases", "disorders pharynx", "Diseases, Pharynx", "Pharynx Disorders", "Pharyngeal Disease", "pharyngeal disease", "Disease of pharynx", "Disorder of pharynx", "Disease, Pharyngeal", "Pharyngeal disorder", "Pharyngeal Disorder", "pharyngeal disorder", "Pharyngeal Diseases", "Diseases of Pharynx", "disorder of pharynx", "Diseases, Pharyngeal", "Pharyngeal Disorders", "Pharyngeal disorders", "Pharyngeal disorder NOS", "Disease of pharynx, NOS", "DISEASES OF THE PHARYNX", "diseases of the pharynx", "chordate pharynx disease", "diseases disorders pharynx", "disease of chordate pharynx", "disorder of chordate pharynx", "disease (or disorder); pharynx", "Disorder of pharynx (disorder)", "Unspecified disease of pharynx", "disorder of pharynx (diagnosis)", "chordate pharynx disease or disorder", "disease or disorder of chordate pharynx"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of pharynx", "shortest_name_length": 15}
{"curie": "MONDO:0019060", "names": ["Bone Tumor", "bone tumor", "Bone tumor", "BONE TUMOR", "bone tumors", "bone tumour", "Bone Tumors", "Bone tumour", "bone tumours", "Bone neoplasm", "tumor of bone", "osseous tumor", "Bone Neoplasm", "bone neoplasm", "Tumor of Bone", "Bones--Tumors", "Neoplasm bone", "Osseous Tumor", "BONE NEOPLASM", "NEOPLASM BONE", "Skeletal tumor", "Bone neoplasms", "Neoplasm, Bone", "bone neoplasms", "Bone Neoplasms", "rare bone tumor", "Skeletal tumour", "Neoplasms, Bone", "Neoplasm of bone", "Neoplasm of Bone", "osseous neoplasm", "Osseous Neoplasm", "neoplasm of bone", "Tumor of the Bone", "bone tissue tumor", "tumor of the bone", "Bone neoplasm NOS", "primary bone cancer", "tumor of bone tissue", "neoplasm of the bone", "bone tissue neoplasm", "Neoplasm of the Bone", "neoplasm of bone tissue", "Neoplasm of bone (disorder)", "Neoplasm of skeletal system", "neoplasm of skeletal system", "neoplasm of bone (diagnosis)", "Neoplasm of the skeletal system", "Neoplasia of the skeletal system", "primary malignant neoplasm of bone", "Bone tumor (morphologic abnormality)", "Neoplasm of skeletal system (disorder)", "neoplasm of skeletal system (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bone neoplasm", "shortest_name_length": 10}
{"curie": "UMLS:C1333819", "names": ["Glandular Cell Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Glandular Cell Intraepithelial Neoplasia", "shortest_name_length": 40}
{"curie": "UMLS:C1135342", "names": ["Cystic Fibrosis Pulmonary Exacerbation", "Cystic fibrosis pulmonary exacerbation", "Cystic fibrosis with pulmonary exacerbation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cystic fibrosis pulmonary exacerbation", "shortest_name_length": 38}
{"curie": "MONDO:0001410", "names": ["senile vaginitis", "Senile vaginitis", "Vaginitis;senile", "vaginitis atropic", "senile; vaginitis", "vaginitis; senile", "VAGINITIS ATROPIC", "atropic vaginitis", "Atrophic vaginitis", "Atrophic Vaginitis", "vaginitis atrophic", "Vaginitis atrophic", "atrophic vaginitis", "Vaginitis;atrophic", "VAGINITIS ATROPHIC", "ATROPHIC VAGINITIS", "vaginitis; atrophic", "Vaginitis, Atrophic", "atrophic; vaginitis", "Atrophic Vaginitides", "Vaginitides, Atrophic", "Senile atrophic vaginitis", "Senile (atrophic) vaginitis", "Atrophic vaginitis (disorder)", "atrophic vaginitis (diagnosis)", "Postmenopausal atrophic vaginitis", "postmenopausal atrophic vaginitis", "vaginitis; postmenopausal atrophic", "postmenopausal; atrophic vaginitis", "atrophic; vaginitis, postmenopausal", "postmenopausal; vaginitis, atrophic", "postmenopausal atrophic vaginitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postmenopausal atrophic vaginitis", "shortest_name_length": 16}
{"curie": "UMLS:C0339152", "names": ["orbit; emphysema", "emphysema; orbit", "Orbital emphysema", "Orbital Emphysema", "Orbital emphysema (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Orbital emphysema", "shortest_name_length": 16}
{"curie": "MONDO:0011719", "names": ["gant", "gist", "GIST", "GANT", "GISTs", "gants", "gists", "GIST, NOS", "Plexosarcoma", "GIST, Malignant", "GIST, malignant", "GI stroma tumor", "GI stroma tumour", "Gastrointestinal stroma tumor", "gastrointestinal stromal tumor", "Gastrointestinal Stromal Tumor", "Gastrointestinal stromal tumor", "Gastrointestinal stroma tumour", "GASTROINTESTINAL TUMOR STROMAL", "GASTROINTESTINAL STROMAL TUMOR", "Gastrointestinal stromal tumors", "stromal tumor, gastrointestinal", "Gastrointestinal Stromal Tumors", "gastrointestinal stromal tumour", "Gastrointestinal stromal tumour", "Stromal Tumor, Gastrointestinal", "Tumor, Gastrointestinal Stromal", "gastrointestinal stromal tumors", "Stromal Tumors, Gastrointestinal", "gastrointestinal stromal sarcoma", "Tumors, Gastrointestinal Stromal", "Gastrointestinal Stromal Sarcoma", "gastrointestinal stromal tumours", "Gastrointestinal stromal sarcoma", "Gastrointestinal stromal tumours", "gastrointestinal stromal neoplasm", "Gastrointestinal Stromal Neoplasm", "Gastrointestinal Stromal Neoplasms", "Neoplasm, Gastrointestinal Stromal", "Stromal Neoplasm, Gastrointestinal", "Neoplasms, Gastrointestinal Stromal", "Gastrointestinal stromal tumor, NOS", "Stromal Neoplasms, Gastrointestinal", "Gastrointestinal stromal tumor (GIST)", "Gastrointestinal Stromal Tumor (GIST)", "Gastrointestinal pacemaker cell tumor", "GIST - Gastrointestinal stromal tumor", "gastrointestinal stromal tumor (gist)", "Gastrointestinal autonomic nerve tumor", "Gastrointestinal Autonomic Nerve Tumor", "Gastrointestinal pacemaker cell tumour", "GIST - Gastrointestinal stromal tumour", "Stromal tumor of gastrointestinal tract", "Gastrointestinal autonomic nerve tumour", "neoplasm gastrointestinal tract stromal", "stromal tumor of gastrointestinal tract", "Stromal tumour of gastrointestinal tract", "Malignant Gastrointestinal Stromal Tumor", "Gastrointestinal stromal tumor (disorder)", "Gastrointestinal stromal tumor, malignant", "GASTROINTESTINAL STROMAL TUMOR, MALIGNANT", "Gastrointestinal stromal tumour, malignant", "gastrointestinal stromal neoplasm (diagnosis)", "gastrointestinal stromal tumor, isolated cases", "Malignant GIST (gastrointestinal stromal tumor)", "Malignant GIST (gastrointestinal stromal tumour)", "Gastrointestinal stromal tumor (morphologic abnormality)", "gastrointestinal stromal tumor, familial, isolated cases", "Gastrointestinal stromal sarcoma (morphologic abnormality)", "Gastrointestinal stromal tumor, uncertain malignant potential", "Gastrointestinal Stromal Tumor with Neurogenic Differentiation", "Gastrointestinal stromal tumour, uncertain malignant potential", "Gastrointestinal Stromal Tumor of Uncertain Malignant Potential", "Gastrointestinal stromal tumor, uncertain malignant potential (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastrointestinal stromal tumor", "shortest_name_length": 4}
{"curie": "UMLS:C0686467", "names": ["Benign Uvea Tumor", "Benign Uveal Tumor", "Benign Uvea Neoplasm", "Benign Tumor of Uvea", "Benign Uveal Neoplasm", "Benign Neoplasm of Uvea", "Benign Tumor of the Uvea", "Benign Uveal Tract Neoplasm", "Benign Neoplasm of the Uvea", "Benign neoplasm of uveal tract", "benign neoplasm of uveal tract", "Benign neoplasm of uveal tract (disorder)", "benign neoplasm of uveal tract (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign neoplasm of uveal tract", "shortest_name_length": 17}
{"curie": "UMLS:C4525201", "names": ["IA", "Stage IA Hepatocellular Cancer", "Stage IA Liver Cell Carcinoma AJCC v8", "Stage IA Hepatocellular Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Hepatocellular Carcinoma AJCC v8", "shortest_name_length": 2}
{"curie": "MONDO:0014456", "names": ["SCN6", "SCN 6-Autosomal Recessive", "severe congenital neutropenia 6", "NEUTROPENIA, SEVERE CONGENITAL, 6, AUTOSOMAL RECESSIVE", "neutropenia, severe congenital, 6, autosomal recessive", "Neutropenia, Severe Congenital, 6, Autosomal Recessive", "Severe Congenital Neutropenia Type 6, Autosomal Recessive", "autosomal recessive severe congenital neutropenia due to JAGN1 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive severe congenital neutropenia due to JAGN1 deficiency", "shortest_name_length": 4}
{"curie": "UMLS:C5420057", "names": ["Sinonasal Epithelioid Hemangioendothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Epithelioid Hemangioendothelioma", "shortest_name_length": 42}
{"curie": "MONDO:0019549", "names": ["AR-CMT2, Ouvrier type", "SEOAN due to MFN2 deficiency", "severe early-onset axonal neuropathy due to MFN2 deficiency", "Severe early-onset axonal neuropathy due to MFN2 deficiency", "Autosomal recessive Charcot-Marie-Tooth disease Ouvrier type", "Autosomal recessive Charcot-Marie-Tooth disease, Ouvrier type", "autosomal recessive Charcot-Marie-Tooth disease, Ouvrier type", "Severe early-onset axonal neuropathy due to mitofusin 2 deficiency", "Severe early-onset axonal neuropathy due to MFN2 (mitofusin 2) deficiency", "Severe early-onset axonal neuropathy due to mitofusin 2 deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe early-onset axonal neuropathy due to MFN2 deficiency", "shortest_name_length": 21}
{"curie": "UMLS:C1300346", "names": ["Collagenous Fibroma", "Collagenous fibroma", "collagenous fibroma", "Desmoplastic fibroblastoma", "Desmoplastic Fibroblastoma", "desmoplastic fibroblastoma", "Desmoplastic fibroblastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Desmoplastic fibroblastoma", "shortest_name_length": 19}
{"curie": "MONDO:0013710", "names": ["HNPCC5", "LYNCH5", "LYNCH SYNDROME 5", "Lynch syndrome 5", "MSH6 hereditary nonpolyposis colon cancer", "hereditary nonpolyposis colorectal cancer type 5", "Colorectal Cancer, Hereditary Nonpolyposis, Type 5", "COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5", "colorectal cancer, hereditary nonpolyposis, type 5", "hereditary nonpolyposis colon cancer caused by mutation in MSH6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lynch syndrome 5", "shortest_name_length": 6}
{"curie": "MONDO:0004308", "names": ["meninges sarcoma", "Meninges Sarcoma", "Meningeal sarcoma", "meningeal sarcoma", "Meningeal Sarcoma", "Sarcoma of Meninges", "sarcoma of meninges", "Meningothelial sarcoma", "sarcoma of the meninges", "Sarcoma of the Meninges", "meningeal cluster sarcoma", "sarcoma of meningeal cluster", "sarcoma of meninges (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "meningeal sarcoma", "shortest_name_length": 16}
{"curie": "UMLS:C4726581", "names": ["Transformed Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transformed Non-Hodgkin Lymphoma", "shortest_name_length": 32}
{"curie": "UMLS:C1704320", "names": ["Minimal Change Glomerulonephritis", "Glomerulonephritis, Minimal Change", "Minimal Change Glomerulonephritides", "Glomerulonephritides, Minimal Change"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Glomerulonephritis, Minimal Change", "shortest_name_length": 33}
{"curie": "UMLS:C0007020", "names": ["CO poisoning", "CO Poisoning", "carbon monoxide poison", "carbon monoxide toxicity", "Toxicity;carbon monoxide", "CARBON MONOXIDE POISONING", "Carbon monoxide poisoning", "Carbon Monoxide Poisoning", "carbon monoxide poisoning", "Poisoning, Carbon Monoxide", "Carbon Monoxide Poisonings", "Monoxide Poisoning, Carbon", "Poisonings, Carbon Monoxide", "Monoxide Poisonings, Carbon", "Carbon monoxide intoxication", "poisoning by carbon monoxide", "Toxic effect of carbon monoxide", "Carbon monoxide poisoning syndrome", "Carbon monoxide causing toxic effect", "poisoning by carbon monoxide (diagnosis)", "Toxic effect of carbon monoxide (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carbon Monoxide Poisoning", "shortest_name_length": 12}
{"curie": "MONDO:0003427", "names": ["Atypical Adenoma", "Atypical adenoma", "bronchus adenoma", "Bronchial adenoma", "BRONCHUS, ADENOMA", "Bronchial Adenoma", "adenoma; bronchus", "bronchus; adenoma", "bronchial adenoma", "Adenoma of bronchus", "Adenoma of Bronchus", "adenoma of bronchus", "BRONCHIAL ADENOMA NOS", "Bronchial adenoma NOS", "Lung Papillary Adenoma", "lung papillary adenoma", "Bronchial adenoma, NOS", "Adenoma of the Bronchus", "adenoma of the bronchus", "Type II Pneumocyte Adenoma", "type II pneumocyte adenoma", "ADENOMA, BRONCHIAL, BENIGN", "Bronchial adenoma syndrome", "adenoma, bronchial, benign", "Bronchial adenoma (disorder)", "Papillary Adenoma of Type II Pneumocytes", "papillary adenoma of type II pneumocytes", "Atypical adenoma (morphologic abnormality)", "bronchial adenoma NOS (morphologic abnormality)", "Peripheral Papillary Tumor of Type II Pneumocytes", "peripheral papillary tumor of type II pneumocytes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bronchus adenoma", "shortest_name_length": 16}
{"curie": "MONDO:0100416", "names": ["AML, FLT3/TKD Point Mutation", "AML, FLT3-TKD Point Mutation", "AML, FLT3 tyrosine kinase domain point mutation", "acute myeloid leukemia, FLT3 tyrosine kinase domain point mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, FLT3 tyrosine kinase domain point mutation", "shortest_name_length": 28}
{"curie": "UMLS:C1519702", "names": ["Turcot Syndrome Type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Turcot Syndrome Type 1", "shortest_name_length": 22}
{"curie": "MONDO:0010561", "names": ["CLS", "Coffin Syndrome", "Coffin syndrome", "Syndrome, Coffin", "Coffin syndrome 2", "Coffin syndrome 1", "soft hands syndrome", "Coffin-Lowry syndrome", "COFFIN-LOWRY SYNDROME", "coffin-lowry syndrome", "COFFIN-Lowry syndrome", "Coffin-Lowry Syndrome", "Coffin Lowry Syndrome", "lean spastic dwarfism", "syndrome coffin lowry", "Lean spastic dwarfism", "coffin lowry syndrome", "Syndrome, Coffin-Lowry", "dwarfism, lean spastic type", "Dwarfism, lean spastic type", "Coffin-Lowry syndrome (CLS)", "CLS - Coffin-Lowry syndrome", "Coffin-Siris-Wegienka syndrome", "Coffin-Lowry syndrome (disorder)", "Coffin-Lowry syndrome (diagnosis)", "Coffin-Lowry syndrome, X-linked dominant", "mental retardation with osteocartilaginous abnormalities", "Mental Retardation with Osteocartilaginous Abnormalities", "intellectual disability with osteocartilaginous abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Coffin-Lowry syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C1708927", "names": ["Somatolactotrope Adenoma", "Somatomammotrope Adenoma", "Mammosomatotrope Adenoma", "Mammosomatotroph Adenoma", "Mammosomatotroph PitNET/Adenoma", "Mammosomatotroph Pituitary Gland Adenoma", "Mammosomatotroph Pituitary Neuroendocrine Tumor", "Mammosomatotroph Pituitary Neuroendocrine Tumor/Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mammosomatotroph Pituitary Neuroendocrine Tumor", "shortest_name_length": 24}
{"curie": "MONDO:0004443", "names": ["Chest Wall Parachordoma", "chest wall parachordoma", "parachordoma of chest wall", "Parachordoma of Chest Wall", "Parachordoma of the Chest Wall", "parachordoma of the chest wall"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chest wall parachordoma", "shortest_name_length": 23}
{"curie": "UMLS:C5206792", "names": ["Refractory Cytomegalovirus Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Cytomegalovirus Infection", "shortest_name_length": 36}
{"curie": "MONDO:0013584", "names": ["HSNIE", "HSN1E", "Hsnie", "HSAN1E", "Hsn Ie", "HSN 1E", "HSN IE", "hereditary sensory neuropathy type IE", "Hereditary Sensory Neuropathy Type Ie", "hereditary sensory neuropathy type 1E", "NEUROPATHY, HEREDITARY SENSORY, TYPE IE", "neuropathy, hereditary sensory, type IE", "neuropathy, hereditary sensory, type 1E", "Hereditary sensory autonomic neuropathy type IE", "Hereditary Sensory and Autonomic Neuropathy Type Ie", "hereditary sensory and autonomic neuropathy type 1E", "DNMT1-related dementia, deafness, and sensory neuropathy", "Dnmt1-Related Dementia, Deafness, and Sensory Neuropathy", "Hereditary sensory neuropathy-deafness-dementia syndrome", "hereditary sensory neuropathy-deafness-dementia syndrome", "Hereditary sensory autonomic neuropathy type IE (disorder)", "hereditary sensory neuropathy with hearing loss and dementia", "neuropathy, hereditary sensory, with hearing loss and dementia", "NEUROPATHY, HEREDITARY SENSORY, WITH HEARING LOSS AND DEMENTIA", "Hereditary sensory neuropathy-sensorineural hearing loss-dementia syndrome", "hereditary sensory neuropathy-sensorineural hearing loss-dementia syndrome", "Hereditary Sensory and Autonomic Neuropathy Type 1 with Dementia and Hearing Loss"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary sensory neuropathy-deafness-dementia syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C5420306", "names": ["Unresectable Peritoneal Biphasic Mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Peritoneal Biphasic Mesothelioma", "shortest_name_length": 45}
{"curie": "UMLS:C5420540", "names": ["Locally Advanced Endometrial Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Endometrial Adenocarcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0030695", "names": ["DEE100", "early infantile epileptic encephalopathy 100", "developmental and epileptic encephalopathy 100", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 100"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy 100", "shortest_name_length": 6}
{"curie": "UMLS:C5419009", "names": ["HPV16 Infection", "HPV-16 Infection", "Human Papillomavirus-16 Infection", "Human Papillomavirus Type 16 Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HPV16 Infection", "shortest_name_length": 15}
{"curie": "UMLS:C5446450", "names": ["Lacrimal Drainage System Adenoid Cystic Carcinoma", "Adenoid Cystic Carcinoma of the Lacrimal Drainage System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lacrimal Drainage System Adenoid Cystic Carcinoma", "shortest_name_length": 49}
{"curie": "UMLS:C0346007", "names": ["Trichoadenoma", "Trichoadenoma (disorder)", "Trichoadenoma of Nikolowski"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Trichoadenoma", "shortest_name_length": 13}
{"curie": "MONDO:0014228", "names": ["FECD8", "AGBL1 Fuchs' endothelial dystrophy", "corneal dystrophy, Fuchs endothelial, 8", "CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 8", "corneal dystrophy, Fuchs endothelial, type 8", "Fuchs' endothelial dystrophy caused by mutation in AGBL1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal dystrophy, Fuchs endothelial, 8", "shortest_name_length": 5}
{"curie": "MONDO:0001442", "names": ["Dysthymia", "dysthymia", "Dysthymia, NOS", "dysthymic disorder", "Dysthymic Disorder", "DYSTHYMIC DISORDER", "dysthymia disorder", "Dysthymic disorder", "dysthymic disorders", "Dysthymic Disorders", "disorder; dysthymic", "dysthymic; disorder", "Disorder, Dysthymic", "Dysthymia (disorder)", "dysthymia (diagnosis)", "Persistent Depressive Disorder, Dysthymia", "persistent depressive disorder (dysthymia)", "Persistent depressive disorder (dysthymia)", "persistent depressive disorder (dysthymia) (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dysthymic disorder", "shortest_name_length": 9}
{"curie": "MONDO:0010554", "names": ["ABERS", "CHARGE-like syndrome", "Abruzzo-Erickson Syndrome", "Abruzzo-Erickson syndrome", "Abruzzo Erickson syndrome", "ABRUZZO-ERICKSON SYNDROME", "CHARGE like syndrome X-linked", "CHARGE-LIKE SYNDROME, X-LINKED", "CHARGE-like syndrome, X-linked", "Charge-Like Syndrome, X-Linked", "CHARGE like syndrome, X linked", "cleft palate-coloboma-deafness syndrome", "Cleft palate-coloboma-deafness syndrome", "Cleft palate-coloboma-hearing loss syndrome", "cleft palate with coloboma of eye and deafness syndrome", "Cleft palate with coloboma of eye and deafness syndrome", "Cleft palate with coloboma of eye and deafness syndrome (disorder)", "cleft palate with coloboma of eye and deafness syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abruzzo-Erickson syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0343467", "names": ["Erythema nodosum leprosum", "erythema nodosum leprosum", "ENL - Erythema nodosum leprosum", "erythema nodosum leprosum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Erythema nodosum leprosum", "shortest_name_length": 25}
{"curie": "MONDO:0001945", "names": ["postencephalitic parkinsonism", "postencephalitic Parkinsonism", "Postencephalitic Parkinsonism", "Postencephalitic parkinsonism", "postencephalitic; parkinsonism", "parkinsonism; postencephalitic", "Parkinsonism post encephalitic", "Parkinsonism, Postencephalitic", "PARKINSONISM, POSTENCEPHALITIC", "postencephalitic Parkinson disease", "Postencephalitic Parkinson Disease", "Parkinson Disease, Postencephalitic", "Post Encephalitic Parkinson Disease", "Post-Encephalitic Parkinson Disease", "Postencephalitic Parkinson's disease", "postencephalitic Parkinson's disease", "Parkinson Disease, Post-Encephalitic", "Parkinson Disease, Post Encephalitic", "Postencephalitis Parkinsonian Syndrome", "Parkinsonian Syndrome, Postencephalitis", "Postencephalitic parkinsonism (disorder)", "Encephalitis Lethargica Type Parkinsonism", "von Economo Encephalitis Type Parkinsonism", "Postencephalitic Economo-Type Parkinsonism", "Postencephalitic Economo Type Parkinsonism", "Parkinsonism, Postencephalitic Economo-Type", "Economo-Type Parkinsonism, Postencephalitic", "postencephalitic Parkinson's disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postencephalitic Parkinson disease", "shortest_name_length": 29}
{"curie": "MONDO:0007447", "names": ["DDU", "VBU", "vibratory angioedema", "Vibratory angioedema", "VIBRATORY ANGIOEDEMA", "Angioedema, vibratory", "Vibratory angio-edema", "angioedema, vibratory", "Vibratory angio-oedema", "Dermodistortive Urticaria", "DERMODISTORTIVE URTICARIA", "dermodistortive urticaria", "Dermo-distortive urticaria", "Vibratory angioedema (disorder)", "autosomal dominant vibratory urticaria", "vibratory urticaria, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant vibratory urticaria", "shortest_name_length": 3}
{"curie": "MONDO:0014989", "names": ["UHS2", "uncombable hair syndrome 2", "UNCOMBABLE HAIR SYNDROME 2", "TGM3 uncombable hair syndrome", "uncombable hair syndrome type 2", "uncombable hair syndrome 2; UHS2", "uncombable hair syndrome caused by mutation in TGM3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uncombable hair syndrome 2", "shortest_name_length": 4}
{"curie": "MONDO:0019366", "names": ["free sialic acid storage disease", "Free sialic acid storage disease", "N-acetylneuraminic acid (NANA) storage disease (NSD)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "free sialic acid storage disease", "shortest_name_length": 32}
{"curie": "EFO:0009964", "names": ["bipolar II disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bipolar II disorder", "shortest_name_length": 19}
{"curie": "MONDO:0008323", "names": ["LIDLS", "LIDLS1", "Liddle Syndrome", "Liddle syndrome", "LIDDLE SYNDROME", "Syndrome, Liddle", "liddle's syndrome", "LIDDLE'S SYNDROME", "Liddle's syndrome", "LIDDLE SYNDROME 1", "pseudoaldosteronism", "PSEUDOALDOSTERONISM", "Pseudoaldosteronism", "Pseudo aldosteronism", "pseudohyperaldosteronism", "Pseudohyperaldosteronism", "PSEUDOHYPERALDOSTERONISM", "Pseudoprimary aldosteronism", "Liddle's syndrome (diagnosis)", "Pseudohyperaldosteronism type 1", "pseudohyperaldosteronism type 1", "Pseudoprimary hyperaldosteronism", "Pseudoprimary hyperaldosteronism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liddle syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0015977", "names": ["IGHM", "agammaglobulinemia", "Agammaglobulinemia", "agammaglobulinaemia", "Agammaglobulinaemia", "Agammaglobulinemias", "antibody Deficiency", "hypogammaglobulinemia", "Agammaglobulinemia NOS", "Agammaglobulinemia, NOS", "Gammaglobulin Deficiency", "mu heavy chain deficiency", "Immunoglobulin Deficiency", "Agammaglobulinemia (finding)", "agammaglobulinemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "agammaglobulinemia", "shortest_name_length": 4}
{"curie": "MONDO:0021273", "names": ["ciliary body leiomyoma", "Ciliary Body Leiomyoma", "Leiomyoma of ciliary body", "Leiomyoma of Ciliary Body", "leiomyoma of ciliary body", "Leiomyoma of the Ciliary Body", "leiomyoma of the ciliary body", "Leiomyoma of ciliary body (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leiomyoma of ciliary body", "shortest_name_length": 22}
{"curie": "MONDO:0019844", "names": ["pituitary hormone deficiency secondary to storage disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pituitary hormone deficiency secondary to storage disease", "shortest_name_length": 57}
{"curie": "UMLS:C0342985", "names": ["superficial bacterial infection of skin", "Superficial bacterial infection of skin", "Superficial bacterial infection of skin (disorder)", "superficial bacterial infection of skin (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Superficial bacterial infection of skin", "shortest_name_length": 39}
{"curie": "MONDO:0020065", "names": ["combined dystonia", "dystonia-plus syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined dystonia", "shortest_name_length": 17}
{"curie": "UMLS:C0162296", "names": ["polyarthralgia", "Polyarthralgia", "POLYARTHRALGIA", "Polyarthralgias", "polyarthralgias", "Arthralgia multiple", "multiple joint pain", "Multiple joint pain", "joints multiple pain", "polyarticular joint pain", "Pain in joint, multiple sites", "arthralgias of multiple sites", "Multiple joint pain (finding)", "Arthralgia of multiple joints", "Pain in a joint, multiple sites", "Pain in joint involving multiple sites", "arthralgias of multiple sites (diagnosis)", "localized joint pain in more than one joint", "localized joint pain in more than one joint (symptom)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Polyarthralgia", "shortest_name_length": 14}
{"curie": "MONDO:0032673", "names": ["IBGC7", "basal ganglia calcification, idiopathic, 7, autosomal recessive", "BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 7, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "basal ganglia calcification, idiopathic, 7, autosomal recessive", "shortest_name_length": 5}
{"curie": "MONDO:0001343", "names": ["kidney disease", "disease of kidney", "impaired renal function disease", "Impaired renal function disorder", "renal impairment; disorder resulting from", "Impaired renal function disorder (disorder)", "Disorders resulting from impaired renal function", "Unspecified disorder resulting from impaired renal function"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "impaired renal function disease", "shortest_name_length": 14}
{"curie": "UMLS:C0854858", "names": ["Recurrent T Lymphoblastic Leukemia/Lymphoma", "Recurrent T-Lymphoblastic Leukemia/Lymphoma", "Relapsed Precursor T Lymphoblastic Lymphoma/Leukemia", "Recurrent Precursor T-Lymphoblastic Lymphoma/Leukemia", "Precursor T-lymphoblastic lymphoma/leukemia recurrent", "Precursor T-lymphoblastic lymphoma/leukaemia recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Precursor T-lymphoblastic lymphoma/leukemia recurrent", "shortest_name_length": 43}
{"curie": "MONDO:0023224", "names": ["inherited reflex epilepsy", "hereditary reflex epilepsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited reflex epilepsy", "shortest_name_length": 25}
{"curie": "UMLS:C0948779", "names": ["Gastrointestinal hypomotility", "Gastrointestinal hypomotility (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal hypomotility", "shortest_name_length": 29}
{"curie": "MONDO:0002491", "names": ["ABUSE", "AOD abuse", "DRUG ABUSE", "Drug abuse", "drug abuse", "Drug Abuse", "harmful use", "Abuse, Drug", "abuse; drugs", "Abuse;drug(s)", "Drug abuse NOS", "Drugs of abuse", "chemical abuse", "harmful AOD use", "Drug abuse, NOS", "Substance abuse", "Substance Abuse", "substance abuse", "RNDx drug abuse", "SUBSTANCE ABUSE", "Abuse, Substance", "Medication abuse", "Substance Abuses", "Drug Use Disorder", "SUBSTANCE_AB PROBLEM", "RNDx substance abuse", "substance abuse drug", "disorder, drug abuse", "Harmful substance use", "dysfunctional AOD use", "Drug abuse (disorder)", "alcohol or drug abuse", "Recreational Drug Use", "drug and alcohol abuse", "drug abuse (diagnosis)", "Substance abuse problem", "abuse (drug or alcohol)", "nondependent drug abuse", "Substance abuse disorder", "Substance Abuse Problems", "substance abuse disorder", "disorder, substance abuse", "Substance abuse (disorder)", "RNDx drug abuse (diagnosis)", "substance abuse (diagnosis)", "alcohol or other drug abuse", "Nondependent abuse of drugs", "Alcohol or Other Drugs abuse", "Nondependent abuse of substance", "RNDx substance abuse (diagnosis)", "substance abuse drug nondependent", "harmful Alcohol or Other Drugs use", "nondependent drug abuse (diagnosis)", "dysfunctional Alcohol or Other Drugs use"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "substance abuse", "shortest_name_length": 5}
{"curie": "MONDO:0014864", "names": ["HMNDYT2", "HYPERMANGANESEMIA WITH DYSTONIA 2", "hypermanganesemia with dystonia 2", "Hypermanganesemia with dystonia 2", "hypermanganesemia with dystonia type 2", "SLC39A14 hypermanganesemia with dystonia", "hypermanganesemia with dystonia 2; HMNDYT2", "HMNDYT2 - hypermanganesemia with dystonia 2", "Hypermanganesemia with dystonia 2 (disorder)", "Hypermanganesemia with dystonia 2 (diagnosis)", "Dystonia-parkinsonism-hypermanganesemia syndrome", "hypermanganesemia with dystonia caused by mutation in SLC39A14", "disorders of manganese metabolism hypermanganesemia with dystonia 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypermanganesemia with dystonia 2", "shortest_name_length": 7}
{"curie": "MONDO:0010208", "names": ["WSS", "WRINKLY SKIN SYNDROME", "Wrinkly skin syndrome", "wrinkly skin syndrome", "wrinkled skin syndrome", "Wrinkled skin syndrome", "wrinkly skin syndrome (WSS)", "WSS - Wrinkly skin syndrome", "Wrinkly skin syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "wrinkly skin syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C0279955", "names": ["stage I grade 2 follicular lymphoma", "Stage I Grade 2 Follicular Lymphoma", "Stage I Grade II Follicular Lymphoma", "Grade II Follicular Lymphoma Stage I", "Follicular Mixed Cell Lymphoma Stage I", "stage I follicular mixed cell lymphoma", "Stage I Follicular Mixed Cell Lymphoma", "follicular mixed cell lymphoma, stage I", "Ann Arbor Stage I Grade 2 Follicular Lymphoma", "Stage I Grade II Follicular Mixed Cell Lymphoma", "Grade II Follicular Mixed Cell Lymphoma Stage I", "stage I grade II follicular mixed cell lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage I Grade 2 Follicular Lymphoma", "shortest_name_length": 35}
{"curie": "UMLS:C4317009", "names": ["diverticular disease", "DIVERTICULAR DISEASE", "Diverticular disease", "Diverticular Disease", "Diverticular Diseases", "DD - Diverticular disease", "Disease;diverticular;intestine", "Diverticular disease (disorder)", "Diverticular disease of intestine", "Diverticular disease of intestine NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diverticular Diseases", "shortest_name_length": 20}
{"curie": "MONDO:0011991", "names": ["DFNB38", "autosomal recessive deafness 38", "DEAFNESS, AUTOSOMAL RECESSIVE 38", "Deafness, Autosomal Recessive 38", "deafness, autosomal recessive 38", "autosomal recessive nonsyndromic deafness 38", "autosomal recessive nonsyndromic hearing loss 38", "autosomal recessive nonsyndromic deafness type 38"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 38", "shortest_name_length": 6}
{"curie": "MONDO:0001394", "names": ["chronic erythremia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic erythremia", "shortest_name_length": 18}
{"curie": "MONDO:0030296", "names": ["MMIHS4", "megacystis-microcolon-intestinal hypoperistalsis syndrome 4", "MEGACYSTIS-MICROCOLON-INTESTINAL HYPOPERISTALSIS SYNDROME 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "megacystis-microcolon-intestinal hypoperistalsis syndrome 4", "shortest_name_length": 6}
{"curie": "UMLS:C0151788", "names": ["Allergic myocarditis", "Myocarditis allergic", "ALLERGIC MYOCARDITIS", "MYOCARDITIS ALLERGIC", "Myocarditis eosinophilic", "Eosinophilic myocarditis", "MYOCARDITIS EOSINOPHILIC", "Eosinophilic myocarditis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eosinophilic myocarditis", "shortest_name_length": 20}
{"curie": "UMLS:C1879314", "names": ["Sertoli-Leydig cell tumor, poorly differentiated", "Poorly Differentiated Ovarian Sertoli-Leydig Cell Tumor", "poorly differentiated Sertoli-Leydig cell tumor of ovary", "Sertoli-Leydig cell tumor, poorly differentiated, of ovary", "poorly differentiated Sertoli-Leydig cell tumor of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Poorly Differentiated Ovarian Sertoli-Leydig Cell Tumor", "shortest_name_length": 48}
{"curie": "UMLS:C4525137", "names": ["Stage IIC Rectal Cancer", "stage IIC rectal cancer", "Stage IIC Rectal Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIC Rectal Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "MONDO:0002739", "names": ["bile duct colloid carcinoma", "Bile Duct Colloid Carcinoma", "colloid bile duct carcinoma", "Colloid Bile Duct Carcinoma", "Bile Duct Colloidal Carcinoma", "bile duct colloidal carcinoma", "colloidal bile duct carcinoma", "Colloidal Bile Duct Carcinoma", "colloid carcinoma of bile duct", "Colloid Carcinoma of Bile Duct", "Mucinous Carcinoma of Bile Duct", "mucinous carcinoma of bile duct", "colloid bile duct adenocarcinoma", "colloidal carcinoma of bile duct", "Colloid Bile Duct Adenocarcinoma", "Colloidal Carcinoma of Bile Duct", "bile duct mucinous adenocarcinoma", "Mucinous Bile Duct Adenocarcinoma", "mucinous bile duct adenocarcinoma", "Bile Duct Mucinous Adenocarcinoma", "Bile duct mucinous adenocarcinoma", "colloidal bile duct adenocarcinoma", "colloid carcinoma of the bile duct", "Colloidal Bile Duct Adenocarcinoma", "Colloid Carcinoma of the Bile Duct", "Colloid Adenocarcinoma of Bile Duct", "colloid adenocarcinoma of bile duct", "Mucinous Carcinoma of the Bile Duct", "mucinous carcinoma of the bile duct", "Colloidal Carcinoma of the Bile Duct", "mucinous adenocarcinoma of bile duct", "Mucinous Adenocarcinoma of Bile Duct", "colloidal carcinoma of the bile duct", "colloidal adenocarcinoma of bile duct", "Colloidal Adenocarcinoma of Bile Duct", "Colloid Adenocarcinoma of the Bile Duct", "colloid adenocarcinoma of the bile duct", "Mucinous Adenocarcinoma of the Bile Duct", "mucinous adenocarcinoma of the bile duct", "Colloidal Adenocarcinoma of the Bile Duct", "colloidal adenocarcinoma of the bile duct", "colloid extrahepatic bile duct adenocarcinoma", "Colloid Extrahepatic Bile Duct Adenocarcinoma", "mucinous extrahepatic bile duct adenocarcinoma", "Mucinous Extrahepatic Bile Duct Adenocarcinoma", "extrahepatic bile duct mucinous adenocarcinoma", "Extrahepatic Bile Duct Mucinous Adenocarcinoma", "Colloidal Extrahepatic Bile Duct Adenocarcinoma", "colloidal extrahepatic bile duct adenocarcinoma", "Colloid Adenocarcinoma of Extrahepatic Bile Duct", "colloid adenocarcinoma of extrahepatic bile duct", "Mucinous Adenocarcinoma of Extrahepatic Bile Duct", "mucinous adenocarcinoma of extrahepatic bile duct", "colloidal adenocarcinoma of extrahepatic bile duct", "Colloidal Adenocarcinoma of Extrahepatic Bile Duct", "colloid adenocarcinoma of the extrahepatic bile duct", "Colloid Adenocarcinoma of the Extrahepatic Bile Duct", "Mucinous Adenocarcinoma of the Extrahepatic Bile Duct", "mucinous adenocarcinoma of the extrahepatic bile duct", "colloidal adenocarcinoma of the extrahepatic bile duct", "Colloidal Adenocarcinoma of the Extrahepatic Bile Duct", "mucinous adenocarcinoma of extrahepatic bile duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extrahepatic bile duct mucinous adenocarcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0010335", "names": ["CORDX3", "cone-rod dystrophy X-linked 3", "X-linked cone-rod dystrophy 3", "cone-rod dystrophy, X-linked, 3", "Cone-Rod Dystrophy, X-Linked, 3", "CONE-ROD DYSTROPHY, X-LINKED, 3", "X-linked cone-rod dystrophy type 3", "cone-rod dystrophy, X-linked, type 3", "cone-rod dystrophy, X-linked, 3, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked cone-rod dystrophy 3", "shortest_name_length": 6}
{"curie": "MONDO:0015779", "names": ["XY/X0", "45,X/46,XY MGD", "45,X0/46,XY MGD", "Mixed Gonadal Dysgenesis", "Mixed gonadal dysgenesis", "45,X/46,XY Gonadal Dysgenesis", "45,X/46,XY gonadal dysgenesis", "45,X/46,XY Mixed Gonadal Dysgenesis", "45,X/46,XY mixed gonadal dysgenesis", "45,X0/46,XY mixed gonadal dysgenesis", "45,X/46,XY disorder of Sex development", "45,X/46,XY Disorder of Sex Development"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "45,X/46,XY mixed gonadal dysgenesis", "shortest_name_length": 5}
{"curie": "UMLS:C5667407", "names": ["Second primary tumor", "Second Primary Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Second Primary Tumor", "shortest_name_length": 20}
{"curie": "MONDO:0003447", "names": ["Clear cell hidradenoma", "Clear Cell Hidradenoma", "clear cell hidradenoma", "clear cell; hidradenoma", "hidradenoma; clear cell", "Clear cell myoepithelioma", "clear cell myoepithelioma", "[M]Clear cell hidradenoma", "Clear cell sweat gland adenoma", "clear cell hidradenoma (morphologic abnormality)", "Clear cell hidradenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "clear cell hidradenoma", "shortest_name_length": 22}
{"curie": "MONDO:0002051", "names": ["integumentary disease", "Disorder of integument", "disorder of integument", "integumental system disease", "integumentary system disease", "integumentary system disorder", "disease of integumental system", "integumentary system disease\"@e", "disorder of integumental system", "Disorder of integument (disorder)", "disorder of integument (diagnosis)", "integumental system disease or disorder", "disease or disorder of integumental system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "integumentary system disorder", "shortest_name_length": 21}
{"curie": "UMLS:C0333870", "names": ["Mild Squamous Cell Atypia", "Mild squamous cell atypia", "Mild squamous cell atypia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mild squamous cell atypia", "shortest_name_length": 25}
{"curie": "MONDO:0012240", "names": ["NEM4", "CAPM2", "Cap myopathy 2", "CAP myopathy 2", "CAP MYOPATHY 2", "NEMALINE MYOPATHY 4", "nemaline myopathy 4", "Nemaline Myopathy 4", "Nemaline myopathy 4", "TPM2 nemaline myopathy", "nemaline myopathy type 4", "nemaline myopathy 4, autosomal dominant", "nemaline myopathy caused by mutation in TPM2", "Nemaline myopathy caused by mutation in the tropomyosin 2 gene"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nemaline myopathy 4", "shortest_name_length": 4}
{"curie": "MONDO:0014832", "names": ["MRT53", "GPIBD13", "NEDHSCA", "PIGG-CDG", "MRT53, FORMERLY", "mental retardation, autosomal recessive 53", "intellectual disability, autosomal recessive 53", "mental retardation, autosomal recessive type 53", "GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 13", "glycosylphosphatidylinositol biosynthesis defect 13", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 53, FORMERLY", "intellectual disability, autosomal recessive type 53", "intellectual developmental disorder, autosomal recessive 53", "congenital disorder of glycosylation due to PIGG deficiency", "early-onset epilepsy-intellectual disability-brain anomalies syndrome", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 53, FORMERLY", "NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPOTONIA, SEIZURES, AND CEREBELLAR ATROPHY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 53", "shortest_name_length": 5}
{"curie": "MONDO:0004486", "names": ["endocervical type cervical adenomyoma", "cervical adenomyoma, endocervical type", "Cervical Adenomyoma, Endocervical Type", "Cervical Adenomyoma, Endocervical-Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endocervical type cervical adenomyoma", "shortest_name_length": 37}
{"curie": "MONDO:0020336", "names": ["EDMD2", "autosomal dominant Emery-Dreifuss muscular dystrophy", "Emery-Dreifuss muscular dystrophy, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant Emery-Dreifuss muscular dystrophy", "shortest_name_length": 5}
{"curie": "MONDO:0010809", "names": ["familial CML-like syndrome", "CML-LIKE SYNDROME, FAMILIAL", "CML-like syndrome, familial", "Cml-Like Syndrome, Familial", "familial chronic myelocytic leukemia-like syndrome", "Myelocytic leukemia-like syndrome, familial, chronic", "myelocytic leukemia-like syndrome, familial, chronic", "MYELOCYTIC LEUKEMIA-LIKE SYNDROME, FAMILIAL, CHRONIC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial chronic myelocytic leukemia-like syndrome", "shortest_name_length": 26}
{"curie": "UMLS:C4054123", "names": ["Rare Neoplastic Syndrome", "Rare Tumor-Associated Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rare Neoplastic Syndrome", "shortest_name_length": 24}
{"curie": "MONDO:0004848", "names": ["Mouth rot", "Ulcerative stomatitis", "Ulcerative Stomatitis", "STOMATITIS ULCERATIVE", "ULCERATIVE STOMATITIS", "Stomatitis ulcerative", "ulcerative stomatitis", "STOMATITIS, ULCERATIVE", "Stomatitis, Ulcerative", "Ulcerative stomatitis (disorder)", "ulcerative stomatitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ulcerative stomatitis", "shortest_name_length": 9}
{"curie": "UMLS:C2931082", "names": ["Hereditary hypoceruloplasminemia", "Familial apoceruloplasmin deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Familial apoceruloplasmin deficiency", "shortest_name_length": 32}
{"curie": "MONDO:0011190", "names": ["NPH2", "Nph2", "NPHP2", "NEPHRONOPHTHISIS 2", "Nephronophthisis 2", "nephronophthisis 2", "nephronophthisis type 2", "Infantile nephronophthisis", "Nephronophthisis, Infantile", "infantile nephronophthisis 2", "nephronophthisis 2, infantile", "INVS nephronophthisis (disease)", "Autosomal recessive infantile NPHP", "Infantile nephronophthisis (disorder)", "Autosomal recessive infantile nephronophthisis", "nephronophthisis (disease) caused by mutation in INVS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephronophthisis 2", "shortest_name_length": 4}
{"curie": "UMLS:C5420234", "names": ["Head and Neck Melanocytic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Head and Neck Melanocytic Neoplasm", "shortest_name_length": 34}
{"curie": "MONDO:0022380", "names": ["acute lymphoblastic leukemia congenital sporadic aniridia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute lymphoblastic leukemia congenital sporadic aniridia", "shortest_name_length": 57}
{"curie": "UMLS:C3146259", "names": ["Stage IV Nasopharyngeal Carcinoma", "Stage IV Nasopharyngeal Throat Cancer", "Stage IV Nasopharyngeal Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Nasopharyngeal Carcinoma AJCC v7", "shortest_name_length": 33}
{"curie": "MONDO:0008398", "names": ["SALIVARY SUBSTANCE, CLOSTRIDIUM BOTULINUM TYPE", "salivary substance, Clostridium botulinum type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "salivary substance, Clostridium botulinum type", "shortest_name_length": 46}
{"curie": "MONDO:0005676", "names": ["Borna Disease", "borna disease", "Borna disease", "Enzootic encephalomyelitis", "enzootic encephalomyelitis", "Near eastern equine encephalomyelitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "borna disease", "shortest_name_length": 13}
{"curie": "MONDO:0021762", "names": ["acrocoxomesomelic dysplasia", "acro-coxo-mesomelic dwarfism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acrocoxomesomelic dysplasia", "shortest_name_length": 27}
{"curie": "MONDO:0017719", "names": ["gangliosidoses", "gangliosidosis", "Gangliosidoses", "Gangliosidosis", "Gangliosidosis NOS", "Gangliosidosis, NOS", "Disease, Gangliosidosis", "Gangliosidosis (disorder)", "gangliosidosis (diagnosis)", "Unspecified gangliosidosis", "ganglioside storage disease", "Ganglioside storage disease", "Ganglioside Storage Disease", "ganglioside storage diseases", "Ganglioside Storage Diseases", "Storage Disease, Ganglioside", "Ganglioside Storage Disorder", "Storage Disorder, Ganglioside", "Ganglioside Storage Disorders", "Storage Diseases, Ganglioside", "Storage Disorders, Ganglioside", "Ganglioside storage disease, NOS", "Ganglioside accumulation in nervous tissue lysosomes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gangliosidosis", "shortest_name_length": 14}
{"curie": "MONDO:0019990", "names": ["fibrillary glomerulonephritis", "Non-amyloid fibrillary glomerulopathy", "non-amyloid fibrillary glomerulopathy", "non-amyloid fibrillary glomerulonephritis", "Non-amyloid fibrillary glomerulonephritis", "Congo red-negative amyloidosis-like glomerulopathy", "Congo red negative amyloidosis like glomerulopathy", "Non-amyloid fibrillary glomerulonephritis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-amyloid fibrillary glomerulopathy", "shortest_name_length": 29}
{"curie": "UMLS:C0438624", "names": ["eye black", "Black eye", "black eye", "bruise eye", "black eyes", "EYE BRUISE", "blacks eye", "eye bruise", "bruises eye", "eye contusion", "Bruise of eye", "contusion eye", "Eye contusion", "EYE CONTUSION", "eye; contusion", "Black eye, NOS", "contusion; eye", "contusions eye", "ecchymosis; eye", "eye; ecchymosis", "Contusion of eye", "contusion of eye", "EYE INJURY BRUISE", "eyeball contusion", "eyeball; contusion", "Injury;contusion;eye", "contusion of ocular eye", "Contusion of eye (disorder)", "Contusion of eye (diagnosis)", "Unspecified contusion of eye", "Contusion of eye, unspecified", "Black eye, not otherwise specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Contusion of eye", "shortest_name_length": 9}
{"curie": "MONDO:0001913", "names": ["Oligospermia", "oligospermia", "OLIGOSPERMIA", "Oligozoospermia", "oligozoospermia", "Low Sperm Count", "Low sperm count", "Low sperm counts", "Sperm Count, Low", "Oligospermia NOS", "Low Sperm Counts", "Sperm Counts, Low", "hypospermatogenesis", "Hypospermatogenesis", "HYPOSPERMATOGENESIS", "Hypospermatogeneses", "oligospermia (diagnosis)", "Oligoasthenoteratozoospermia", "Oligoasthenoteratozoospermias"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oligospermia", "shortest_name_length": 12}
{"curie": "UMLS:C4744714", "names": ["Advanced Prostate Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Prostate Adenocarcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C0496920", "names": ["ovarian neoplasm uncertain behavior", "Neoplasm of uncertain behavior of ovary", "Neoplasm of uncertain behaviour of ovary", "ovarian neoplasm of borderline malignancy", "ovarian neoplasm uncertain behavior (diagnosis)", "Neoplasm of uncertain behavior of ovary (disorder)", "Neoplasm of uncertain or unknown behavior of ovary", "Neoplasm of uncertain or unknown behaviour of ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplasm of uncertain or unknown behavior of ovary", "shortest_name_length": 35}
{"curie": "UMLS:C1334702", "names": ["Mesonephric Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mesonephric Hyperplasia", "shortest_name_length": 23}
{"curie": "MONDO:0002230", "names": ["ovary Wilms tumor", "ovarian Wilms tumor", "Ovarian Wilms Tumor", "ovarian Wilms' tumor", "ovarian Wilms' cancer", "Ovarian Nephroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian Wilms tumor", "shortest_name_length": 17}
{"curie": "MONDO:0013591", "names": ["EDM6", "multiple epiphyseal dysplasia 6", "EPIPHYSEAL DYSPLASIA, MULTIPLE, 6", "epiphyseal dysplasia, multiple, 6", "epiphyseal dysplasia, multiple, type 6", "COL9A1 multiple epiphyseal dysplasia (disease)", "multiple epiphyseal dysplasia (disease) caused by mutation in COL9A1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epiphyseal dysplasia, multiple, 6", "shortest_name_length": 4}
{"curie": "MONDO:0011978", "names": ["CoQ-RESPONSIVE OXPHOS DEFICIENCY", "CoQ-responsive OXPHOS deficiency", "CoQ-responsive oxidative phosphorylation disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CoQ-responsive OXPHOS deficiency", "shortest_name_length": 32}
{"curie": "UMLS:C1336393", "names": ["Stage IVC Hypopharynx Epidermoid Carcinoma", "Stage IVC Epidermoid Carcinoma of Hypopharynx", "Stage IVC Hypopharynx Squamous Cell Carcinoma", "Stage IVC Hypopharyngeal Epidermoid Carcinoma", "Stage IVC Hypopharyngeal Squamous Cell Carcinoma", "Stage IVC Squamous Cell Carcinoma of Hypopharynx", "Stage IVC Epidermoid Carcinoma of the Hypopharynx", "Stage IVC Squamous Cell Carcinoma of the Hypopharynx", "Stage IVC Hypopharyngeal Throat Squamous Cell Cancer", "Stage IVC Hypopharyngeal Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Hypopharyngeal Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 42}
{"curie": "UMLS:C0948299", "names": ["Application site discharge"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Application site discharge", "shortest_name_length": 26}
{"curie": "UMLS:C1335992", "names": ["Small Intestinal Somatostatin-Producing NET", "Small Intestinal Somatostatin Producing Tumor", "Small Intestinal Somatostatin-Producing Neuroendocrine Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Intestinal Somatostatin-Producing Neuroendocrine Tumor", "shortest_name_length": 43}
{"curie": "UMLS:C1707301", "names": ["Heart Monophasic Synovial Sarcoma", "Cardiac Monophasic Synovial Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiac Monophasic Synovial Sarcoma", "shortest_name_length": 33}
{"curie": "MONDO:0018575", "names": ["microcephalic primordial dwarfism-insulin resistance syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephalic primordial dwarfism-insulin resistance syndrome", "shortest_name_length": 61}
{"curie": "MONDO:0009906", "names": ["Prenatal Bowing", "PRENATAL BOWING", "prenatal bowing"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prenatal bowing", "shortest_name_length": 15}
{"curie": "UMLS:C0877523", "names": ["Acquired Megacephaly", "Acquired macrocephaly", "Acquired Macrocephaly", "Acquired Megalocephaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired macrocephaly", "shortest_name_length": 20}
{"curie": "MONDO:0014904", "names": ["CDG1AA", "congenital disorder of glycosylation Iaa", "congenital disorder of glycosylation 1aa", "congenital disorder of glycosylation, type IAA", "congenital disorder of glycosylation, type 1aa", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iaa", "congenital disorder of glycosylation, type IAA; CDG1AA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital disorder of glycosylation, type IAA", "shortest_name_length": 6}
{"curie": "UMLS:C0949856", "names": ["Oxidative Phosphorylation Deficiency", "Deficiency, Oxidative Phosphorylation", "Phosphorylation Deficiency, Oxidative", "Oxidative Phosphorylation Deficiencies", "Deficiencies, Oxidative Phosphorylation", "Phosphorylation Deficiencies, Oxidative"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oxidative Phosphorylation Deficiencies", "shortest_name_length": 36}
{"curie": "UMLS:C0007862", "names": ["Cervicobrachial neuralgia", "Cervicobrachial Neuralgia", "Cervico-Brachial Neuralgia", "Cervico Brachial Neuralgia", "Cervicobrachial Neuralgias", "Cervico-brachial neuralgia", "Neuralgia, Cervicobrachial", "Cervico-Brachial Neuralgias", "Neuralgias, Cervicobrachial", "Neuralgia, Cervico-Brachial", "Neuralgias, Cervico-Brachial", "Cervicobrachial neuralgia (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervico-Brachial Neuralgia", "shortest_name_length": 25}
{"curie": "UMLS:C5238387", "names": ["Metastatic Nasal Cavity Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Nasal Cavity Squamous Cell Carcinoma", "shortest_name_length": 47}
{"curie": "UMLS:C0278698", "names": ["stage III pediatric hepatoma", "stage III childhood hepatoma", "group III childhood hepatoma", "Stage III Pediatric Hepatoma", "group III pediatric hepatoma", "Stage III Childhood Hepatoma", "childhood hepatoma, group III", "pediatric hepatoma, stage III", "pediatric hepatoma, group III", "childhood hepatoma, stage III", "hepatoma, childhood, group III", "hepatoma, pediatric, group III", "hepatoma, pediatric, stage III", "hepatoma, childhood, stage III", "Stage III Hepatocellular Cancer", "group III pediatric liver cancer", "group III childhood liver cancer", "stage III childhood liver cancer", "stage III pediatric liver cancer", "childhood liver cancer, group III", "pediatric liver cancer, stage III", "childhood liver cancer, stage III", "pediatric liver cancer, group III", "liver cancer, childhood, group III", "liver cancer, pediatric, group III", "liver cancer, childhood, stage III", "liver cancer, pediatric, stage III", "Stage III Pediatric Liver Cell Carcinoma", "Stage III Childhood Liver Cell Carcinoma", "Stage III Childhood Hepatocellular Carcinoma", "Stage III Pediatric Hepatocellular Carcinoma", "Stage III Childhood Hepatocellular Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Childhood Hepatocellular Carcinoma AJCC v7", "shortest_name_length": 28}
{"curie": "MONDO:0014787", "names": ["CCAFCA", "BIRK-FLUSSER SYNDROME", "Birk-Flusser syndrome", "corpus callosum, agenesis of, with Facial anomalies and cerebellar ataxia", "corpus callosum, agenesis OF, with FACIAL anomalies and cerebellar ataxia", "CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA", "Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome", "severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome", "Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome", "Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C5557171", "names": ["Stage IIA2 Cervical Cancer AJCC v9", "Stage IIA2 Cervical Carcinoma AJCC v9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA2 Cervical Cancer AJCC v9", "shortest_name_length": 34}
{"curie": "MONDO:0016762", "names": ["Microcornea corectopia macular hypoplasia", "microcornea corectopia macular hypoplasia", "microcornea-corectopia-macular hypoplasia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcornea-corectopia-macular hypoplasia syndrome", "shortest_name_length": 41}
{"curie": "MONDO:0021374", "names": ["cerebral tumor", "Cerebral Tumor", "Cerebral Neoplasm", "cerebral neoplasm", "Tumor of Cerebrum", "tumor of cerebrum", "cerebral neoplasms", "Cerebral Neoplasms", "telencephalon tumor", "neoplasm of cerebrum", "Neoplasm of Cerebrum", "Neoplasm of cerebrum", "Tumor of the Cerebrum", "tumor of the cerebrum", "tumor of telencephalon", "neoplasm of the cerebrum", "Neoplasm of the Cerebrum", "neoplasm of telencephalon", "cerebral hemisphere tumor", "Cerebral Hemispheric Tumor", "cerebral hemispheric tumor", "cerebral hemisphere neoplasm", "tumor of cerebral hemisphere", "cerebral hemispheric neoplasm", "Cerebral Hemispheric Neoplasm", "Tumor of Cerebral Hemispheres", "tumor of cerebral hemispheres", "neoplasm of cerebral hemisphere", "Neoplasm of cerebrum (disorder)", "neoplasm of cerebral hemispheres", "Neoplasm of Cerebral Hemispheres", "telencephalon neoplasm (disease)", "tumor of the cerebral hemispheres", "Tumor of the Cerebral Hemispheres", "neoplasm of the cerebral hemispheres", "Neoplasm of the Cerebral Hemispheres"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplasm of cerebral hemisphere", "shortest_name_length": 14}
{"curie": "UMLS:C3273131", "names": ["Intrahepatic Bile Duct BilIN", "Intrahepatic Bile Duct Dysplasia", "Intrahepatic Bile Duct Biliary Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intrahepatic Bile Duct Biliary Intraepithelial Neoplasia", "shortest_name_length": 28}
{"curie": "UMLS:C1706790", "names": ["Peripheral Ameloblastic Carcinoma", "Ameloblastic Carcinoma-Secondary Type (Dedifferentiated), Peripheral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ameloblastic Carcinoma-Secondary Type (Dedifferentiated), Peripheral", "shortest_name_length": 33}
{"curie": "UMLS:C0339177", "names": ["foreign body; conjunctiva", "conjunctival foreign body", "Conjunctival foreign body", "conjunctiva; foreign body", "Conjunctival Foreign Body", "foreign body of conjunctiva", "Conjunctival foreign body (disorder)", "foreign body of conjunctiva (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conjunctival foreign body", "shortest_name_length": 25}
{"curie": "MONDO:0032771", "names": ["PGL7", "PARAGANGLIOMAS 7", "paragangliomas 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paragangliomas 7", "shortest_name_length": 4}
{"curie": "MONDO:0010265", "names": ["SGBS2", "Sgbs2", "OFD1 Simpson-Golabi-Behmel syndrome", "Simpson-Golabi-Behmel syndrome type 2", "Simpson-Golabi-Behmel syndrome, type 2", "SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2", "Simpson-Golabi-Behmel Syndrome, Type 2", "lethal variant of Simpson-Golabi-Behmel syndrome", "SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2 (disorder)", "Simpson-Golabi-Behmel syndrome caused by mutation in OFD1", "Simpson-Golabi-Behmel syndrome, type 2, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Simpson-Golabi-Behmel syndrome type 2", "shortest_name_length": 5}
{"curie": "MONDO:0013123", "names": ["ASD6", "Atrial Septal Defect 6", "ATRIAL SEPTAL DEFECT 6", "atrial septal defect 6", "atrial septal defect type 6", "atrial heart septal defect 6", "atrial septal defect 6 - ASD6", "TLL1 atrial heart septal defect", "atrial heart septal defect type 6", "atrial septal defect 6 - ASD6 (diagnosis)", "atrial heart septal defect caused by mutation in TLL1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial septal defect 6", "shortest_name_length": 4}
{"curie": "UMLS:C1336243", "names": ["Stage III Bone Sarcoma", "Stage III Sarcoma of Bone", "Stage III Sarcoma of the Bone", "Stage III Bone Sarcoma AJCC v7", "Stage III Bone Sarcoma  AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Bone Sarcoma AJCC v7", "shortest_name_length": 22}
{"curie": "MONDO:0016641", "names": ["Hecht Scott syndrome", "Hecht-Scott syndrome", "Limb deficiency-heart malformation syndrome", "limb transversal defect-cardiac anomaly syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "limb transversal defect-cardiac anomaly syndrome", "shortest_name_length": 20}
{"curie": "MONDO:0016218", "names": ["GBS", "aidp", "PNS neuronitis", "Guillain-Barré", "Barré-Guillain", "LANDRY PARALYSIS", "paralysis; Landry", "Landry; paralysis", "landry's paralysis", "Landry's paralysis", "polyneuritis; acute", "ascending paralysis", "Ascending paralysis", "PARALYSIS ASCENDING", "Paralysis ascending", "ASCENDING PARALYSIS", "PARALYSIS, ASCENDING", "ascending; paralysis", "paralysis; ascending", "Infectious neuronitis", "Landry-Guillain-Barré", "GULLIAN BARRE SYNDROME", "GUILLAIN BARRE DISEASE", "guillain-barre disease", "GUILLAIN-BARRE DISEASE", "GUILLAIN-BARRE SYNDROME", "Guillain Barre syndrome", "Guillain Barré syndrome", "Guillain-Barre Syndrome", "Syndrome Guillain-Barre", "GUILLAIN BARRE SYNDROME", "Guillain Barre Syndrome", "polyneuritis; infective", "Infectious polyneuritis", "guillain-barre syndrome", "Guillain-Barré Syndrome", "Guillain Barré Syndrome", "infective; polyneuritic", "Guillain-Barré syndrome", "Guillain-Barre syndrome", "SYNDROME GUILLAIN-BARRE", "guillain barre syndrome", "Syndrome, Guillain-Barre", "Guillain-Barré Syndromes", "Guillaine-Barre Syndrome", "Guillaine Barre Syndrome", "Syndrome, Guillain-Barré", "KUSSMAUL-LANDRY PARALYSIS", "KUSSMAUL LANDRY PARALYSIS", "Syndrome, Guillaine-Barre", "postinfective; polyneuritic", "Postinfectious polyneuritis", "postinfectious polyneuritis", "Acute Autoimmune Neuropathy", "post-infective polyneuritis", "polyneuritis; postinfective", "Neuropathy, Acute Autoimmune", "Post-infectious polyneuritis", "Acute Infective Polyneuritis", "Autoimmune Neuropathy, Acute", "post-infectious polyneuritis", "Landry's ascending paralysis", "acute infective polyneuritis", "Acute infective polyneuritis", "Acute Autoimmune Neuropathies", "Acute idiopathic polyneuritis", "GBS - Guillain-Barre syndrome", "acute inflammatory neuropathy", "POLYNEURITIS, ACUTE INFECTIVE", "acute idiopathic polyneuritis", "guillain-barre syndrome (GBS)", "Acute inflammatory neuropathy", "acute infectious polyneuritis", "Ascending paralysis (finding)", "Acute Infectious Polyneuritis", "Guillain-Barré-Strohl syndrome", "Guillain-Barre-Strohl syndrome", "Landry Guillain Barre Syndrome", "Infectious Polyneuritis, Acute", "Landry-Guillain-Barré syndrome", "Autoimmune Neuropathies, Acute", "Landry-Guillain-Barre Syndrome", "Landry-Guillain-Barre syndrome", "POLYNEURITIS, ACUTE IDIOPATHIC", "Polyneuritis, Acute Infectious", "Syndrome, Landry-Guillain-Barre", "Acute inflammatory polyneuropathy", "Guillain-Barré syndrome (disorder)", "Guillain-Barre syndrome (diagnosis)", "acute postinfectious polyneuropathy", "acute immune-mediated polyneuropathy", "neuritis; multiple, infective, acute", "multiple; neuritis, infective, acute", "Landry-Guillain-Barre-Strohl syndrome", "Acute idiopathic polyradiculoneuritis", "acute autoimmune peripheral neuropathy", "Acute infective polyneuritis (disorder)", "Post-infectious polyneuritis (disorder)", "Acute post-infective radiculoneuropathy", "acute infectious polyneuritis (diagnosis)", "acute inflammatory demyelinating polyneuropathy", "acute inflammatory demyelinating polyradiculopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Guillain-Barre syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0009424", "names": ["BARTS2", "Bartter disease type 2", "KCNJ1 Bartter syndrome", "Bartter syndrome type 2", "Bartter syndrome type II", "Bartter syndrome, type 2", "Bartter's syndrome type 2", "HYPERPROSTAGLANDIN E SYNDROME 2", "Hyperprostaglandin E syndrome 2", "hyperprostaglandin E syndrome 2", "Bartter syndrome antenatal type 2", "Bartter syndrome type 2 antenatal", "Bartter syndrome, type 2, antenatal", "Bartter syndrome, antenatal, type 2", "Bartter Syndrome, Antenatal, Type 2", "BARTTER SYNDROME, TYPE 2, ANTENATAL", "Hyperprostaglandin E syndrome type 2", "Bartter syndrome, antenatal , type 2", "Bartter syndrome caused by mutation in KCNJ1", "Bartter syndrome antenatal type 2 (disorder)", "Bartter syndrome antenatal type 2 (diagnosis)", "hypokalemic alkalosis with hypercalciuria 2 antenatal", "hypokalemic alkalosis with hypercalciuria antenatal 2", "hypokalemic alkalosis with hypercalciuria 2, antenatal", "Hypokalemic alkalosis with hypercalciuria, antenatal 2", "HYPOKALEMIC ALKALOSIS WITH HYPERCALCIURIA 2, ANTENATAL", "Hypokalemic Alkalosis With Hypercalciuria, Antenatal, 2", "hypokalemic alkalosis with hypercalciuria, antenatal, 2", "Hypokalemic alkalosis with hypercalciuria antenatal type 2", "Hypokalaemic alkalosis with hypercalciuria antenatal type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bartter disease type 2", "shortest_name_length": 6}
{"curie": "MONDO:0007813", "names": ["SEI", "IBS", "ichthyosis exfoliativa", "Ichthyosis Bullous Type", "Bullous Type Ichthyoses", "bullous type ichthyosis", "Bullous Type Ichthyosis", "Ichthyosis, Bullous Type", "Ichthyoses, Bullous Type", "ICHTHYOSIS, BULLOUS TYPE", "ichthyosis, bullous type", "Bullous Type of Ichthyosis", "bullous type of ichthyosis", "Siemens Ichthyosis Bullosa", "Ichthyosis Bullosa of Siemens", "ICHTHYOSIS BULLOSA OF SIEMENS", "ichthyosis bullosa of Siemens", "Ichthyosis bullosa of Siemens", "Ichthyosis, Bullous Type of Siemens", "Superficial epidermolytic ichthyosis", "superficial epidermolytic ichthyosis", "Ichthyosis bullosa of Siemens (disorder)", "bullous congenital ichthyosiform erythroderma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "superficial epidermolytic ichthyosis", "shortest_name_length": 3}
{"curie": "MONDO:0011652", "names": ["PHMDS", "22q13 deletion", "monosomy 22q13", "Monosomy 22q13", "22q13.3 deletion", "Monosomy 22q13.3", "monosomy type 22q13", "22q13 Deletion Syndrome", "22q13 deletion syndrome", "monosomy 22q13 syndrome", "Deletion 22q13 Syndrome", "PHELAN-McDermid syndrome", "PHELAN-MCDERMID SYNDROME", "Phelan-McDermid Syndrome", "Phelan-McDermid syndrome", "Phelan McDermid syndrome", "22q13.3 deletion syndrome", "22q13.3 Deletion Syndrome", "deletion 22q13.3 syndrome", "Deletion 22q13.3 Syndrome", "TELOMERIC 22q13 MONOSOMY SYNDROME", "telomeric 22Q13 monosomy syndrome", "Telomeric 22q13 Monosomy Syndrome", "22q13 deletion syndrome (diagnosis)", "22q13.3 deletion syndrome (disorder)", "chromosome 22Q13.3 deletion syndrome", "Chromosome 22q13.3 Deletion Syndrome", "CHROMOSOME 22q13.3 DELETION SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Phelan-McDermid syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0278695", "names": ["Relapsed Neuroblastoma", "Neuroblastoma recurrent", "recurrent neuroblastoma", "Recurrent Neuroblastoma", "neuroblastoma, recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neuroblastoma recurrent", "shortest_name_length": 22}
{"curie": "UMLS:C0522253", "names": ["Benign exertion headache", "Exertion-induced headache", "Benign exertional headache", "Benign Exertional Headache", "benign exertional headache", "primary exertional headache", "Primary Exertional Headache", "Headache, Benign Exertional", "Exertional Headache, Benign", "Benign Exertional Headaches", "Primary exertional headache", "Headache, Primary Exertional", "Headaches, Benign Exertional", "Exertional Headaches, Benign", "Benign exertional headache (finding)", "primary exertional headache (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Exertional Headache", "shortest_name_length": 24}
{"curie": "MONDO:0003672", "names": ["true posterior wall infarction", "True posterior wall infarction", "infarction myocardial posterior", "Posterior myocardial infarction", "MYOCARDIAL INFARCTION POSTERIOR", "posterior myocardial infarction", "myocardial infarction true posterior", "true posterior myocardial infarction", "True posterior myocardial infarction", "MYOCARDIAL INFARCTION (TRUE POSTERIOR)", "True posterior myocardial infarction (disorder)", "Acute myocardial infarction, strictly posterior", "True posterior myocardial infarction (diagnosis)", "Acute myocardial infarction, true posterior wall infarction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "posterior myocardial infarction", "shortest_name_length": 30}
{"curie": "MONDO:0020506", "names": ["Ovarioleucodystrophy", "ovarioleukodystrophy", "OVARIOLEUKODYSTROPHY", "Ovarioleukodystrophy", "Ovarioleukodystrophy (disorder)", "Vanishing White Matter Leukodystrophy with Ovarian Failure", "VANISHING WHITE MATTER LEUKODYSTROPHY WITH OVARIAN FAILURE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarioleukodystrophy", "shortest_name_length": 20}
{"curie": "MONDO:0004305", "names": ["parathyroid oncocytic adenoma", "Parathyroid Oncocytic Adenoma", "Parathyroid Gland Oxyphilic Adenoma", "Parathyroid Gland Oncocytic Adenoma", "parathyroid gland oncocytic adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parathyroid oncocytic adenoma", "shortest_name_length": 29}
{"curie": "MONDO:0100072", "names": ["neonatal diabetes, congenital sensorineural hearing loss and congenital cataracts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal diabetes, congenital sensorineural hearing loss and congenital cataracts", "shortest_name_length": 81}
{"curie": "MONDO:0009033", "names": ["TEMTYS", "TEMTAMY syndrome", "TEMTAMY SYNDROME", "temtamy syndrome", "Temtamy syndrome", "Temtamy Syndrome", "Temtamy-Shalash syndrome", "Temtamy Shalash syndrome", "Dysmorphism, corpus callosum agenesis and colobomas", "dysmorphism, corpus callosum agenesis and colobomas", "craniofacial dysmorphism-coloboma-corpus callosum agenesis syndrome", "Craniofacial dysmorphism-coloboma-corpus callosum agenesis syndrome", "Craniofacial dysmorphism with coloboma of eye and corpus callosum agenesis syndrome", "Craniofacial dysmorphism with ocular coloboma absent corpus callosum and aortic dilatation", "craniofacial dysmorphism with ocular coloboma absent corpus callosum and aortic dilatation", "Craniofacial Dysmorphism With Ocular Coloboma, Absent Corpus Callosum, And Aortic Dilatation", "Craniofacial dysmorphism with coloboma of eye and corpus callosum agenesis syndrome (disorder)", "Craniofacial dysmorphism with coloboma of eye and corpus callosum agenesis syndrome (diagnosis)", "MENTAL RETARDATION WITH OR WITHOUT CRANIOFACIAL DYSMORPHISM, OCULAR COLOBOMA, OR ABNORMAL CORPUS CALLOSUM", "mental retardation with or without craniofacial Dysmorphism, ocular coloboma, or abnormal corpus callosum", "intellectual disability with or without craniofacial Dysmorphism, ocular coloboma, or abnormal corpus callosum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "temtamy syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C0156309", "names": ["organic impotence", "Organic impotence", "Impotence;organic", "organic; impotence", "impotence; organic origin", "Impotence of organic origin", "Organic erectile dysfunction", "organic impotence (diagnosis)", "Male Erectile Disorder Due to Specified Medical Condition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Impotence of organic origin", "shortest_name_length": 17}
{"curie": "MONDO:0004408", "names": ["Schwannian stroma-rich and stroma-poor composite ganglioneuroblastoma", "schwannian stroma-rich and stroma-poor composite ganglioneuroblastoma", "composite ganglioneuroblastoma, Schwannian Stroma-rich and Stroma-poor", "Composite Ganglioneuroblastoma, Schwannian Stroma-Rich and Stroma-Poor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schwannian stroma-rich and stroma-poor composite ganglioneuroblastoma", "shortest_name_length": 69}
{"curie": "MONDO:0008235", "names": ["Pheochromocytoma Islet Cell Tumor Syndrome", "pheochromocytoma-islet cell tumor syndrome", "PHEOCHROMOCYTOMA--ISLET CELL TUMOR SYNDROME", "pheochromocytoma--islet cell tumor syndrome", "pheochromocytoma and islet cell tumor of the pancreas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pheochromocytoma-islet cell tumor syndrome", "shortest_name_length": 42}
{"curie": "UMLS:C1321632", "names": ["Venous thrombosis deep limb", "Venous thrombosis deep (limbs)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Venous thrombosis deep (limbs)", "shortest_name_length": 27}
{"curie": "UMLS:C1335573", "names": ["Pulmonary Precancerous Condition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pulmonary Precancerous Condition", "shortest_name_length": 32}
{"curie": "MONDO:0012806", "names": ["EPAID2", "EDAID2", "ECTODERMAL DYSPLASIA AND IMMUNODEFICIENCY 2", "ectodermal dysplasia and immunodeficiency 2", "Ectodermal Dysplasia and Immunodeficiency 2", "Autosomal Dominant Anhidrotic Ectodermal Dysplasia", "Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency 2", "ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH IMMUNODEFICIENCY 2", "ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH IMMUNODEFICIENCY 2", "Ectodermal Dysplasia, Hypohidrotic, with Immunodeficiency 2", "ectodermal dysplasia, anhidrotic, with T-cell immunodeficiency, autosomal dominant", "ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH T-CELL IMMUNODEFICIENCY, AUTOSOMAL DOMINANT", "Ectodermal Dysplasia, Anhidrotic, with T-Cell Immunodeficiency, Autosomal Dominant", "Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia and immunodeficiency 2", "shortest_name_length": 6}
{"curie": "UMLS:C2700115", "names": ["Primary Cutaneous Peripheral T-Cell Lymphoma, Rare Subtype"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Cutaneous Peripheral T-Cell Lymphoma, Rare Subtype", "shortest_name_length": 58}
{"curie": "MONDO:0001676", "names": ["EPP", "protoporphyria", "Protoporphyria", "erythropoietic protoporphyria", "Protoporphyria, Erythropoietic", "EPP (erythropoietic protoporphyria porphyria)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythropoietic protoporphyria", "shortest_name_length": 3}
{"curie": "MONDO:0010388", "names": ["RESDX", "Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked", "ROLANDIC EPILEPSY, MENTAL RETARDATION, AND SPEECH DYSPRAXIA, X-LINKED", "ROLANDIC epilepsy, mental retardation, and speech dyspraxia, X-linked", "rolandic epilepsy, mental retardation, and speech dyspraxia, X-linked", "ROLANDIC epilepsy, intellectual disability, and speech dyspraxia, X-linked", "rolandic epilepsy, intellectual disability, and speech dyspraxia, X-linked", "rolandic epilepsy, impaired intellectual development, and speech dyspraxia", "ROLANDIC EPILEPSY, IMPAIRED INTELLECTUAL DEVELOPMENT, AND SPEECH DYSPRAXIA, X-LINKED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rolandic epilepsy, intellectual disability, and speech dyspraxia, X-linked", "shortest_name_length": 5}
{"curie": "MONDO:0016038", "names": ["CAF", "Keasby tumor", "Keasbey tumor", "Keasbey tumour", "Keasbey's tumor", "Keasbey's tumour", "calcified fibroma", "Calcifying fibroma", "aponeurotic fibroma", "Aponeurotic Fibroma", "Juvenile aponeurotic fibroma", "Juvenile aponeurotic fibrosis", "calcified aponeurotic fibroma", "Juvenile Aponeurotic Fibrosis", "calcifying aponeurotic fibroma", "Calcifying aponeurotic fibroma", "Calcifying Aponeurotic Fibroma", "Juvenile aponeurotic fibromatosis", "juvenile aponeurotic fibromatosis", "Juvenile palmo-plantar fibromatosis", "Juvenile aponeurotic fibroma (disorder)", "Calcifying aponeurotic fibroma (disorder)", "Juvenile aponeurotic fibroma (morphologic abnormality)", "Calcifying aponeurotic fibroma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "calcified aponeurotic fibroma", "shortest_name_length": 3}
{"curie": "MONDO:0060777", "names": ["cervical fibroepithelial polyp", "Cervical Fibroepithelial Polyp", "Cervical fibroepithelial polyp", "Uterine Cervix Fibroepithelial Polyp", "uterine cervix fibroepithelial polyp"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical fibroepithelial polyp", "shortest_name_length": 30}
{"curie": "MONDO:0017098", "names": ["FCD type Ic", "isolated focal cortical dysplasia type Ic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated focal cortical dysplasia type Ic", "shortest_name_length": 11}
{"curie": "UMLS:C1335312", "names": ["Pancreatic Non-Hodgkin Lymphoma", "Pancreatic Non-Hodgkin's Lymphoma", "Primary Pancreatic Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Non-Hodgkin Lymphoma", "shortest_name_length": 31}
{"curie": "MONDO:0007624", "names": ["FLYNN-AIRD SYNDROME", "Flynn Aird syndrome", "flynn-aird syndrome", "Flynn-Aird Syndrome", "flynn aird syndrome", "Flynn-Aird syndrome", "Flynn-Aird syndrome (disorder)", "cataracts, retinitis pigmentosa, sensorineural hearing loss, ataxia, peripheral neuritis, epilepsy, dementia, skin atrophy, chronic ulceration, dental"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Flynn-Aird syndrome", "shortest_name_length": 19}
{"curie": "UMLS:C5418912", "names": ["Unresectable Fallopian Tube Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Fallopian Tube Carcinoma", "shortest_name_length": 37}
{"curie": "UMLS:C0266089", "names": ["Cheilognathoschisis", "CHEILOGNATHOSCHISIS", "cheilognathoschisis", "Cleft lip and cleft jaw", "Cleft lip AND cleft jaw", "Cheilognathoschisis (disorder)", "cheilognathoschisis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cheilognathoschisis", "shortest_name_length": 19}
{"curie": "MONDO:0006646", "names": ["angiomyoma", "Angiomyoma", "Angiomyomas", "Angioleiomyoma", "angioleiomyoma", "Angioleiomyomas", "Vascular leiomyoma", "Vascular Leiomyoma", "vascular leiomyoma", "Leiomyoma, Vascular", "Vascular Leiomyomas", "Leiomyomas, Vascular", "Angiomyoma (morphologic abnormality)", "angiomyoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angioleiomyoma", "shortest_name_length": 10}
{"curie": "MONDO:0031280", "names": ["Stuve-Wiedemann syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stuve-Wiedemann syndrome", "shortest_name_length": 24}
{"curie": "UMLS:C5446449", "names": ["Lacrimal Drainage System Mucoepidermoid Carcinoma", "Mucoepidermoid Carcinoma of the Lacrimal Drainage System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lacrimal Drainage System Mucoepidermoid Carcinoma", "shortest_name_length": 49}
{"curie": "MONDO:0002921", "names": ["Myotubular Myopathy", "Myopathy, Myotubular", "Myotubular Myopathies", "Centronuclear Myopathy", "Myopathies, Myotubular", "centronuclear myopathy", "congenital structural myopathy", "Congenital Structural Myopathy", "Myopathy, Congenital Structural", "Structural Myopathy, Congenital", "Congenital Structural Myopathies", "Myopathies, Congenital Structural", "Structural Myopathies, Congenital", "Myopathies, Structural, Congenital", "Congenital Non-Progressive Myopathy", "Non-Progressive Myopathy, Congenital", "Myopathy, Congenital Non-Progressive", "Congenital Non Progressive Myopathies", "Congenital Non-Progressive Myopathies", "Myopathies, Congenital Non-Progressive", "Non Progressive Myopathies, Congenital", "Non-Progressive Myopathies, Congenital"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital structural myopathy", "shortest_name_length": 19}
{"curie": "MONDO:0014951", "names": ["MRT74", "SOTOS3", "SOTOS3, FORMERLY", "Sotos syndrome 3", "APC2 Sotos syndrome", "Sotos syndrome type 3", "SOTOS SYNDROME 3, FORMERLY", "Sotos syndrome caused by mutation in APC2", "autosomal recessive intellectual developmental disorder 74", "intellectual developmental disorder, autosomal recessive 74", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 74"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sotos syndrome 3", "shortest_name_length": 5}
{"curie": "UMLS:C1960925", "names": ["EGFR positive non-small cell lung cancer", "EGF-R positive non-small cell lung cancer", "Epidermal growth factor receptor positive non-small cell lung cancer", "Non-small cell lung cancer, positive for epidermal growth factor receptor expression", "Non-small cell lung cancer, positive for epidermal growth factor receptor expression (disorder)", "Non-small cell lung cancer, positive for epidermal growth factor receptor expression (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epidermal growth factor receptor positive non-small cell lung cancer", "shortest_name_length": 40}
{"curie": "MONDO:0001474", "names": ["Chronic salpingo-oophoritis", "chronic salpingo-oophoritis", "salpingo-oophoritis; chronic", "salpingo-oophoritis, chronic", "chronic; salpingo-oophoritis", "chronic salpingitis/oophoritis", "Chronic salpingitis and oophoritis", "chronic salpingitis and oophoritis", "Chronic salpingo-oophoritis (disorder)", "chronic salpingo-oophoritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic salpingo-oophoritis", "shortest_name_length": 27}
{"curie": "MONDO:0010312", "names": ["Rrdx", "RRDX", "radial ray deficiency", "Radial Ray Deficiency, X-Linked", "radial ray deficiency, X-linked", "RADIAL RAY DEFICIENCY, X-LINKED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radial ray deficiency, X-linked", "shortest_name_length": 4}
{"curie": "MONDO:0002938", "names": ["skin Metatypical carcinoma", "Skin Metatypical Carcinoma", "skin metatypical carcinoma", "basosquamous carcinoma of skin", "Basosquamous carcinoma of skin", "metatypical basal cell carcinoma", "Skin Metatypical Basal Cell Carcinoma", "skin metatypical basal cell carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metatypical basal cell carcinoma", "shortest_name_length": 26}
{"curie": "UMLS:C0221384", "names": ["Follicular conjunctivitis", "CONJUNCTIVITIS, FOLLICULAR", "follicular; conjunctivitis", "conjunctivitis; follicular", "Follicular conjunctivitis, NOS", "Follicular conjunctivitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Follicular conjunctivitis", "shortest_name_length": 25}
{"curie": "UMLS:C5237325", "names": ["Localized Malignant Pancreatic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized Malignant Pancreatic Neoplasm", "shortest_name_length": 39}
{"curie": "UMLS:C4521868", "names": ["Stage IIB Ampulla of Vater Cancer", "Stage IIB Ampulla of Vater Cancer AJCC v8", "Stage IIB Ampulla of Vater Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Ampulla of Vater Cancer AJCC v8", "shortest_name_length": 33}
{"curie": "UMLS:C1868725", "names": ["Perineal infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perineal infection", "shortest_name_length": 18}
{"curie": "UMLS:C1516063", "names": ["Astler-Coller B2 Colorectal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Astler-Coller B2 Colorectal Carcinoma", "shortest_name_length": 37}
{"curie": "UMLS:C1334461", "names": ["Salivary Gland Lymphoepithelial Carcinoma", "Lymphoepithelial Salivary Gland Carcinoma", "lymphoepithelial squamous cell carcinoma of salivary gland", "lymphoepithelial squamous cell carcinoma of salivary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphoepithelial squamous cell carcinoma of salivary gland", "shortest_name_length": 41}
{"curie": "UMLS:C5206805", "names": ["Advanced Bone Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Bone Sarcoma", "shortest_name_length": 21}
{"curie": "UMLS:C0729519", "names": ["Upper respiratory bacterial infection", "Bacterial upper respiratory infection", "upper respiratory infection bacterial", "Bacterial upper respiratory infection (disorder)", "Bacterial upper respiratory infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bacterial upper respiratory infection", "shortest_name_length": 37}
{"curie": "MONDO:0017672", "names": ["focal PPK", "focal keratosis palmoplantaris", "focal palmoplantar keratoderma", "focal palmoplantar hyperkeratosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal palmoplantar keratoderma", "shortest_name_length": 9}
{"curie": "MONDO:0004210", "names": ["colon L-cell glucagon-like peptide-producing NET", "Colon L-Cell Glucagon-Like Peptide-Producing NET", "colonic L-cell glucagon-like peptide producing tumor", "Colon L-Cell Glucagon-Like Peptide-Producing Neuroendocrine Tumor", "colon L-cell glucagon-like peptide-producing neuroendocrine tumor", "colonic L-cell glucagon-like peptide-producing neuroendocrine tumor", "Colonic L-Cell Glucagon-Like Peptide-Producing Neuroendocrine Tumor", "L-cell glucagon-like peptide-producing neuroendocrine tumor of colon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colonic L-cell glucagon-like peptide producing tumor", "shortest_name_length": 48}
{"curie": "MONDO:0001096", "names": ["Mediastinal Ganglioneuroblastoma", "mediastinal ganglioneuroblastoma", "mediastinum ganglioneuroblastoma", "Ganglioneuroblastoma of mediastinum", "Ganglioneuroblastoma of Mediastinum", "ganglioneuroblastoma of mediastinum", "Ganglioneuroblastoma of the Mediastinum", "ganglioneuroblastoma of the mediastinum", "mediastinum ganglioneuroblastoma (disease)", "ganglioneuroblastoma (disease) of mediastinum", "ganglioneuroblastoma of mediastinum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mediastinum ganglioneuroblastoma", "shortest_name_length": 32}
{"curie": "UMLS:C4086157", "names": ["Childhood Nodular Ganglioneuroblastoma", "Childhood Ganglioneuroblastoma, Nodular"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Ganglioneuroblastoma, Nodular", "shortest_name_length": 38}
{"curie": "MONDO:0019009", "names": ["Epilepsy due to FCD", "epilepsy due to FCD", "Isolated focal cortical dysplasia", "isolated focal cortical dysplasia", "Isolated focal cortical dysplasia (disorder)", "Isolated focal cortical dysplasia (diagnosis)", "congenital malformation brain cortical dysplasia localized isolated focal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated focal cortical dysplasia", "shortest_name_length": 19}
{"curie": "MONDO:0007952", "names": ["Maxillofacial Dysostosis", "maxillofacial dysostosis", "MAXILLOFACIAL DYSOSTOSIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maxillofacial dysostosis", "shortest_name_length": 24}
{"curie": "MONDO:0002099", "names": ["Darling's disease", "darling's disease", "American histoplasmosis", "Histoplasmosis, American", "histoplasmosis; American", "classical histoplasmosis", "Classical histoplasmosis", "American; histoplasmosis", "Small form histoplasmosis", "small form histoplasmosis", "Histoplasma capsulatum Infection", "Histoplasma capsulatum infection", "Histoplasma capsulatum Infections", "Infection, Histoplasma capsulatum", "infection by Histoplasma capsulatum", "Infection by Histoplasma capsulatum", "small form histoplasmosis (diagnosis)", "Histoplasmosis capsulati, unspecified", "Histoplasma capsulatum; histoplasmosis", "histoplasmosis; Histoplasma capsulatum", "Histoplasma capsulatum infectious disease", "Infection caused by Histoplasma capsulatum", "infection caused by Histoplasma capsulatum", "Histoplasma capsulatum disease or disorder", "histoplasmosis due to Histoplasma capsulatum", "Histoplasma capsulatum caused disease or disorder", "Infection caused by Histoplasma capsulatum (disorder)", "histoplasmosis due to Histoplasma capsulatum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Histoplasma capsulatum infectious disease", "shortest_name_length": 17}
{"curie": "MONDO:0009095", "names": ["Kirghizian Dermatoosteolysis", "Kirghizian dermatoosteolysis", "KIRGHIZIAN DERMATOOSTEOLYSIS", "Dermatoosteolysis Kirghizian type", "Dermatoosteolysis, Kirghizian type", "DERMATOOSTEOLYSIS, KIRGHIZIAN TYPE", "dermatoosteolysis, Kirghizian type", "Dermatoosteolysis, Kirghizian Type", "Dermatoosteolysis Kirghizian type (disorder)", "autosomal recessive syndrome of skin ulceration, arthroosteolysis with pseudoacromegaly, keratitis, and oligodontia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermatoosteolysis, Kirghizian type", "shortest_name_length": 28}
{"curie": "OMIM:614193", "names": ["TFQTL2", "TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 6}
{"curie": "MONDO:0017628", "names": ["Myospherulosis", "myospherulosis", "spherulocytosis", "Spherulocytosis", "Myospherulosis (disorder)", "subcutaneous spherulocystic disease", "Subcutaneous spherulocystic disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myospherulosis", "shortest_name_length": 14}
{"curie": "UMLS:C0238056", "names": ["chorea senile", "Senile Chorea", "Senile chorea", "senile chorea", "CHOREA, SENILE", "Senile Choreas", "chorea; senile", "Chorea, Senile", "senile; chorea", "Choreas, Senile", "senile chorea (diagnosis)", "CHOREA, CHRONIC PROGRESSIVE NONHEREDITARY", "Chronic progressive non-hereditary chorea", "Chronic progressive non-hereditary chorea (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chorea, Senile", "shortest_name_length": 13}
{"curie": "DOID:0081250", "names": ["CIC-DUX Sarcoma", "CIC-Rearranged Sarcoma", "CIC-rearranged sarcoma", "CIC-rearranged sarcoma (morphologic abnormality)", "Capicua transcriptional repressor (CIC)-rearranged sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CIC-rearranged sarcoma", "shortest_name_length": 15}
{"curie": "MONDO:0005971", "names": ["staphyloenterotoxemia", "staphyloenterotoxicosis", "poisoning; staphylococcus", "staphylococcus; poisoning", "staphylococcal food poison", "staphylococcal food poisoning", "Staphylococcal food poisoning", "Staphylococcal Food Poisoning", "Staphylococcal Food Poisonings", "FOOD POISONING, STAPHYLOCOCCAL", "Poisoning, Staphylococcal Food", "Food poisoning, staphylococcal", "Food Poisoning, Staphylococcal", "Poisonings, Staphylococcal Food", "Food Poisonings, Staphylococcal", "Staphylococcal toxemia due to food", "Staphylococcal toxaemia due to food", "staphylococcal toxaemia due to food", "Food poisoning due to staphylococcus", "Foodborne staphylococcal intoxication", "Staphylococcal toxemia caused by food", "Staphylococcal toxaemia caused by food", "poisoning; food, due to Staphylococcus", "food; poisoning, due to Staphylococcus", "Food poisoning caused by staphylococcus", "Staphylococcal toxemia specified as due to food", "Staphylococcal toxaemia specified as due to food", "Staphylococcal toxemia specified as caused by food", "Food poisoning caused by staphylococcus (disorder)", "Staphylococcal toxaemia specified as caused by food"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "staphyloenterotoxemia", "shortest_name_length": 21}
{"curie": "UMLS:C5230925", "names": ["Mucosal nodular melanoma", "Mucosal Nodular Melanoma", "Nodular melanoma of mucous membrane", "Nodular melanoma of mucous membrane (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mucosal nodular melanoma", "shortest_name_length": 24}
{"curie": "MONDO:0008253", "names": ["Spontaneous platelet aggregation", "platelet aggregation, spontaneous", "PLATELET AGGREGATION, SPONTANEOUS", "Platelet Aggregation, Spontaneous"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "platelet aggregation, spontaneous", "shortest_name_length": 32}
{"curie": "MONDO:0009754", "names": ["lethal congenital neutropenia with eosinophilia", "neutropenia lethal congenital with eosinophilia", "NEUTROPENIA, LETHAL CONGENITAL, WITH EOSINOPHILIA", "Neutropenia, Lethal Congenital, with Eosinophilia", "neutropenia, lethal congenital, with eosinophilia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neutropenia, lethal congenital, with eosinophilia", "shortest_name_length": 47}
{"curie": "UMLS:C0022333", "names": ["Rolandic march", "Jacksonian seizure", "jacksonian seizure", "JACKSONIAN SEIZURE", "Jacksonian Seizure", "seizure; jacksonian", "JACKSONIAN SEIZURES", "Jacksonian seizures", "Seizure, Jacksonian", "jacksonian seizures", "jacksonian's seizure", "Seizure (Jacksonian)", "jacksonian; seizures", "Seizure(s) Jacksonian", "jacksonian; epileptic", "Convulsion Jacksonian", "CONVULSION JACKSONIAN", "convulsions; jacksonian", "Jacksonian seizure, NOS", "jacksonian; convulsions", "Simple partial seizure with focal motor signs with march", "Simple partial seizure with focal motor signs with march (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jacksonian Seizure", "shortest_name_length": 14}
{"curie": "UMLS:C0496930", "names": ["bladder neoplasm of uncertain behavior", "neoplasm of uncertain behavior of bladder", "Neoplasm of uncertain behavior of bladder", "Neoplasm of uncertain behaviour of bladder", "Neoplasm of uncertain behavior of bladder, NOS", "Neoplasm of uncertain behaviour of bladder, NOS", "Neoplasm of uncertain behavior of bladder (disorder)", "Neoplasm of uncertain or unknown behavior of bladder", "neoplasm of uncertain behavior of bladder (diagnosis)", "Neoplasm of uncertain or unknown behaviour of bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplasm of uncertain or unknown behavior of bladder", "shortest_name_length": 38}
{"curie": "UMLS:C0879594", "names": ["Oral Complications of Chemotherapy and Head and Neck Radiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral Complications of Chemotherapy and Head and Neck Radiation", "shortest_name_length": 62}
{"curie": "MONDO:0017214", "names": ["adenosylcobalamin deficiency", "Adenosylcobalamin deficiency", "Methylmalonic aciduria, type II", "Adenosylcobalamin synthesis defect", "Adenosylcobalamin synthesis defect, NOS", "Vitamin B12-responsive methylmalonic aciduria", "Vitamin B12-responsive methylmalonic acidemia", "Adenosylcobalamin synthesis defect (disorder)", "vitamin B12-responsive methylmalonic aciduria", "vitamin B12-responsive methylmalonic acidemia", "Vitamin B12-responsive methylmalonic acidaemia", "methylmalonic aciduria, vitamin B12, responsive", "methylmalonic aciduria, vitamin B12, responsive (diagnosis)", "Methylmalonic acidemia due to defects in adenosylcobalamin biosynthesis", "Methylmalonic acidaemia due to defects in adenosylcobalamin biosynthesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitamin B12-responsive methylmalonic acidemia", "shortest_name_length": 28}
{"curie": "UMLS:C0341779", "names": ["Chlamydial epididymitis", "chlamydial epididymitis", "Chlamydial epididymitis (disorder)", "Chlamydia; epididymitis (etiology)", "chlamydial epididymitis (diagnosis)", "epididymitis; chlamydial (etiology)", "Chlamydia; epididymitis (manifestation)", "epididymitis; chlamydial (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chlamydial epididymitis", "shortest_name_length": 23}
{"curie": "UMLS:C0276755", "names": ["Onychomycosis due to Trichophyton mentagrophytes", "Onychomycosis caused by Trichophyton mentagrophytes", "Onychomycosis caused by Trichophyton mentagrophytes (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Onychomycosis due to Trichophyton mentagrophytes", "shortest_name_length": 48}
{"curie": "MONDO:0018465", "names": ["Hirata disease", "autoimmune insulin syndrome", "Insulin autoimmune syndrome", "insulin autoimmune syndrome", "insulin autoimmune hypoglycemia", "Insulin autoimmune syndrome (disorder)", "autoimmune insulin syndrome (diagnosis)", "autoimmune endocrine disease insulin syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "insulin autoimmune syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C1697135", "names": ["Infusion site cellulitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infusion site cellulitis", "shortest_name_length": 24}
{"curie": "UMLS:C3898896", "names": ["Hemodialysis Catheter-Associated Bacteremia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemodialysis Catheter-Associated Bacteremia", "shortest_name_length": 43}
{"curie": "UMLS:C5419417", "names": ["Recognised Device or Procedural Complication", "Recognized Device or Procedural Complication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recognized Device or Procedural Complication", "shortest_name_length": 44}
{"curie": "UMLS:C0268385", "names": ["Jewish type amyloid polyneuropathy", "Jewish Type Familial Amyloid Polyneuropathy", "Familial amyloid polyneuropathy, Jewish type", "Familial Amyloid Polyneuropathy, Jewish Type", "Familial amyloid polyneuropathy, 33 Ile-for-Phe", "Familial amyloid polyneuropathy, Jewish type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Familial Amyloid Polyneuropathy, Jewish Type", "shortest_name_length": 34}
{"curie": "UMLS:C0476073", "names": ["papillary tumor", "Papillary Tumor", "Papillary tumor", "Papillary tumour", "neoplasm papillary", "Papillary neoplasm", "Papillary Neoplasm", "papillary neoplasms", "Papillary neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Papillary neoplasm", "shortest_name_length": 15}
{"curie": "UMLS:C4724875", "names": ["Refractory Indolent Adult Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Indolent Adult Non-Hodgkin Lymphoma", "shortest_name_length": 46}
{"curie": "UMLS:C0279835", "names": ["oropharynx cancer, stage II", "Stage II Oropharyngeal Cancer", "Stage II Oropharynx Carcinoma", "stage II oropharyngeal cancer", "Oropharyngeal cancer stage II", "oropharyngeal cancer, stage II", "Oropharyngeal Cancer, Stage II", "Stage II Oropharyngeal Carcinoma", "Stage II Carcinoma of Oropharynx", "Stage II Carcinoma of the Oropharynx", "Stage II Oropharyngeal Throat Cancer", "Stage II Oropharyngeal Carcinoma AJCC v6", "Stage II Oropharyngeal Carcinoma AJCC v7", "Stage II Oropharyngeal Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Oropharyngeal Carcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0100422", "names": ["AML, AML1 Mutation", "AML, AML1 Gene Mutation", "AML, CBFalpha2 Mutation", "AML, RUNX1 gene mutation", "AML, CBFA2 Gene Mutation", "AML, AMLCR1 Gene Mutation", "Acute Myeloid Leukemia with Mutated RUNX1", "Acute myeloid leukemia with mutated RUNX1", "acute myeloid leukemia with mutated RUNX1", "Acute Myeloid Leukemia with RUNX1 Mutation", "Acute myeloid leukaemia with mutated RUNX1", "Provisional entity: AML with mutated RUNX1", "acute myeloid leukemia, RUNX1 gene mutation", "AML, Acute Myeloid Leukemia 1 Gene Mutation", "Acute Myeloid Leukemia with Non-Germline Mutated RUNX1", "AML, Runt-Related Transcription Factor 1 Gene Mutation", "Acute myeloid leukemia with mutated RUNX1 (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, RUNX1 gene mutation", "shortest_name_length": 18}
{"curie": "UMLS:C5206466", "names": ["Resectable Colorectal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Colorectal Carcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C1142358", "names": ["Lactic acidosis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lactic acidosis syndrome", "shortest_name_length": 24}
{"curie": "MONDO:0002453", "names": ["Retrocochlear Disease", "retrocochlear disease", "Disease, Retrocochlear", "Retrocochlear Diseases", "Diseases, Retrocochlear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retrocochlear disease", "shortest_name_length": 21}
{"curie": "MONDO:0017338", "names": ["MMDS", "Multiple mitochondrial dysfunctions syndrome", "Multiple Mitochondrial Dysfunctions Syndrome", "multiple mitochondrial dysfunctions syndrome", "fatal multiple mitochondrial dysfunction syndrome", "fatal multiple mitochondrial dysfunctions syndrome", "MMDS - multiple mitochondrial dysfunctions syndrome", "Multiple mitochondrial dysfunctions syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fatal multiple mitochondrial dysfunctions syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0009853", "names": ["Gräsbeck-Imerslund disease", "Imerslund-Grasbeck syndrome", "Imerslund-Gräsbeck syndrome", "congenital pernicious anemia", "Congenital pernicious anemia", "Congenital pernicious anaemia", "juvenile megaloblastic Anemia", "Familial megaloblastic anemia", "familial megaloblastic anemia", "Pernicious (congenital) anemia", "Familial megaloblastic anaemia", "Pernicious anemia, juvenile type", "Congenital pernicious anemia, NOS", "Congenital pernicious anaemia, NOS", "enterocyte cobalamin malabsorption", "Juvenile type megaloblastic anemia", "Juvenile type megaloblastic anaemia", "Juvenile type megaloblastic anemia, NOS", "congenital pernicious anemia (diagnosis)", "Familial megaloblastic anemia (disorder)", "Juvenile type megaloblastic anaemia, NOS", "Juvenile type megaloblastic anemia (disorder)", "defect of enterocyte intrinsic factor receptor", "selective cobalamin malabsorption with proteinuria", "Megaloblastic anemia due to inborn errors of metabolism", "Megaloblastic anaemia due to inborn errors of metabolism", "Megaloblastic anemia due to inborn errors of metabolism, NOS", "Megaloblastic anaemia due to inborn errors of metabolism, NOS", "Megaloblastic anemia due to inborn errors of metabolism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Imerslund-Grasbeck syndrome", "shortest_name_length": 26}
{"curie": "UMLS:C2981633", "names": ["Stage I Hilar Cholangiocarcinoma", "Stage I Hilar Cholangiocarcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Hilar Cholangiocarcinoma AJCC v7", "shortest_name_length": 32}
{"curie": "MONDO:0003059", "names": ["bile duct tumor", "bile duct cancer", "cancer of bile duct", "Ca extrahepatic bile ducts", "malignant bile duct neoplasm", "malignant neoplasm of bile duct", "malignant neoplasm of the extrahepatic bile duct"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bile duct cancer", "shortest_name_length": 15}
{"curie": "UMLS:C3640029", "names": ["Congenital VT", "Congenital VTach", "Congenital Ventricular Tachycardia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Ventricular Tachycardia", "shortest_name_length": 13}
{"curie": "MONDO:0010907", "names": ["HYPTRP", "hypertryptophanemia", "Hypertryptophanemia", "HYPERTRYPTOPHANEMIA", "familial hypertryptophanemia", "Familial hypertryptophanemia", "hypertryptophanemia, familial", "HYPERTRYPTOPHANEMIA, FAMILIAL", "Familial hypertryptophanaemia", "Hypertryptophanemia, Familial", "[OBSOLETE] Hypertryptophanemia", "Familial hypertryptophanemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial hypertryptophanemia", "shortest_name_length": 6}
{"curie": "MONDO:0012388", "names": ["MYP11", "myopia 11", "Myopia 11", "MYOPIA 11, AUTOSOMAL DOMINANT", "myopia 11, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopia 11, autosomal dominant", "shortest_name_length": 5}
{"curie": "MONDO:0015712", "names": ["non-distal trisomy 10q", "non-telomeric trisomy 10q", "non-distal duplication 10q", "non-distal trisomy type 10q"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-distal trisomy 10q", "shortest_name_length": 22}
{"curie": "MONDO:0010462", "names": ["MRXSCS", "mental retardation, X-linked, syndromic, Chudley-Schwartz type", "MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE", "syndromic X-linked intellectual disability Chudley-Schwartz type", "intellectual disability, X-linked, syndromic, Chudley-Schwartz type", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE", "mental retardation, X-linked, syndromic, Chudley-Schwartz type, X-linked recessive", "X-linked mental retardation with seizures, hypogammaglobinemia, and gait disturbance", "MENTAL RETARDATION, X-LINKED, WITH SEIZURES, HYPOGAMMAGLOBULINEMIA, AND GAIT DISTURBANCE", "mental retardation, X-linked, with seizures, hypogammaglobulinemia, and Gait disturbance", "X-linked intellectual disability with seizures, hypogammaglobinemia, and gait disturbance", "intellectual disability, X-linked, with seizures, hypogammaglobulinemia, and Gait disturbance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic X-linked intellectual disability Chudley-Schwartz type", "shortest_name_length": 6}
{"curie": "UMLS:C1334049", "names": ["HPV-Related Anal Squamous Cell Carcinoma", "Human Papillomavirus-Related Anal Squamous Cell Carcinoma", "Human Papilloma Virus Related Anal Squamous Cell Carcinoma", "Human Papilloma Virus-Related Anal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Human Papillomavirus-Related Anal Squamous Cell Carcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0006620", "names": ["mammalian vulva skin tag", "vulva fibroepithelial polyp", "Vulva Fibroepithelial Polyp", "skin tag of mammalian vulva", "Vulval Fibroepithelial Polyp", "vulvar fibroepithelial polyp", "vulval fibroepithelial polyp", "Vulval Fibroepithelial polyp", "Vulvar Fibroepithelial Polyp", "Fibroepithelial Polyp of Vulva", "fibroepithelial polyp of vulva", "Fibroepithelial Polyp of the Vulva", "fibroepithelial polyp of the vulva", "Vulvar Fibroepithelial Stromal Polyp", "vulvar fibroepithelial stromal polyp"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulva fibroepithelial polyp", "shortest_name_length": 24}
{"curie": "MONDO:0013694", "names": ["MRT31", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 31", "mental retardation, autosomal recessive 31", "intellectual disability, autosomal recessive 31", "autosomal recessive intellectual developmental disorder 31", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 31"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 31", "shortest_name_length": 5}
{"curie": "MONDO:0018668", "names": ["scedosporiosis", "Scedosporiosis", "pseudallescheriasis", "Scedosporium infection", "Scedosporiosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scedosporiosis", "shortest_name_length": 14}
{"curie": "MONDO:0007356", "names": ["FCC1", "COCA1", "LYNCH1", "HNPCC1", "Lynch syndrome I", "Lynch 1 Syndrome", "LYNCH syndrome I", "LYNCH SYNDROME 1", "Lynch Syndrome I", "Lynch syndrome 1", "Lynch Syndrome 1", "Lynch syndrome 2", "Lynch 1 syndrome", "Lynch syndrome type 1", "LYNCH SYNDROME I, FORMERLY", "LYNCH SYNDROME II, FORMERLY", "Lynch syndrome I (diagnosis)", "Lynch Cancer Family Syndrome I", "Familial Nonpolyposis Colon Cancer Type 1", "familial nonpolyposis colon cancer type 1", "Familial Non-Polyposis Colon Cancer Type 1", "familial non-polyposis colon cancer type 1", "Colon Cancer, Familial Nonpolyposis, Type 1", "colon cancer, familial nonpolyposis, type 1", "COLON CANCER, FAMILIAL NONPOLYPOSIS, TYPE 1", "Hereditary non-polyposis colon cancer type 1", "Hereditary Non-Polyposis Colon Cancer Type 1", "Lynch syndrome I (site-specific colonic cancer)", "Hereditary Nonpolyposis Colorectal Cancer Type 1", "hereditary nonpolyposis colorectal cancer type 1", "colorectal cancer, hereditary nonpolyposis, type 1", "Colorectal Cancer, Hereditary Nonpolyposis, Type 1", "COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 1", "Colorectal cancer, hereditary nonpolyposis, type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lynch syndrome 1", "shortest_name_length": 4}
{"curie": "UMLS:C5204345", "names": ["Borderline Ovarian Seromucinous Tumor/Atypical Proliferative Ovarian Seromucinous Tumor with Microinvasion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Ovarian Seromucinous Tumor/Atypical Proliferative Ovarian Seromucinous Tumor with Microinvasion", "shortest_name_length": 106}
{"curie": "MONDO:0035159", "names": ["Dermoid or epidermoid cyst of the CNS", "dermoid or epidermoid cyst of the central nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermoid or epidermoid cyst of the central nervous system", "shortest_name_length": 37}
{"curie": "UMLS:C4288807", "names": ["Low Grade Broad Ligament Serous Adenocarcinoma", "Low-Grade Broad Ligament Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Grade Broad Ligament Serous Adenocarcinoma", "shortest_name_length": 46}
{"curie": "MONDO:0009225", "names": ["fever, familial lifelong persistent", "FEVER, FAMILIAL LIFELONG PERSISTENT", "Fever, Familial Lifelong Persistent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fever, familial lifelong persistent", "shortest_name_length": 35}
{"curie": "UMLS:C1708959", "names": ["Mediastinal T-Lymphoblastic Leukemia/Lymphoma", "Mediastinal T Lymphoblastic Leukemia/Lymphoma", "Mediastinal Precursor T-Lymphoblastic Lymphoma/Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mediastinal T Lymphoblastic Leukemia/Lymphoma", "shortest_name_length": 45}
{"curie": "MONDO:0003036", "names": ["MEC", "MUCC", "Mucoepidermoid tumor", "mucoepidermoid tumor", "Mucoepidermoid Tumor", "Mucoepidermoid tumour", "Tumor, Mucoepidermoid", "mucoepidermoid tumors", "Mucoepidermoid Tumors", "tumor, mucoepidermoid", "tumors, mucoepidermoid", "Tumors, Mucoepidermoid", "Mucoepidermoid neoplasm", "Mucoepidermoid carcinoma", "MUCOEPIDERMOID NEOPLASMS", "Mucoepidermoid Carcinoma", "mucoepidermoid carcinoma", "Mucoepidermoid Neoplasms", "Mucoepidermoid Carcinomas", "Carcinoma, Mucoepidermoid", "Carcinomas, Mucoepidermoid", "mucoepidermoid carcinoma (diagnosis)", "Mucoepidermoid neoplasm (morphology)", "Mucoepidermoid neoplasm (morphologic abnormality)", "mucoepidermoid carcinoma (morphologic abnormality)", "Mucoepidermoid carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucoepidermoid carcinoma", "shortest_name_length": 3}
{"curie": "UMLS:C5418566", "names": ["Locally Advanced Malignant Female Reproductive System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Malignant Female Reproductive System Neoplasm", "shortest_name_length": 62}
{"curie": "UMLS:C0851341", "names": ["Infestation", "infestation", "infestations", "Infestation NOS", "Infestation, NOS", "parasite infestation", "parasitic infestation", "infestations parasite", "infestations parasitic", "infestation (diagnosis)", "Infestation, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infestation", "shortest_name_length": 11}
{"curie": "MONDO:0009869", "names": ["Robin", "PRBNS", "Pierre Robin", "Robin sequence", "Robin Sequence", "robin sequence", "Robin syndrome", "sequence, Robin", "Sequence, Robin", "robins sequence", "Robin's anomalad", "Robin's syndrome", "Pierre-robin anomaly", "Pierre-Robin sequence", "PIERRE ROBIN SEQUENCE", "pierre-robin syndrome", "Pierre Robin Syndrome", "pierre robin syndrome", "Pierre Robin sequence", "PIERRE ROBIN SYNDROME", "Pierre Robin Sequence", "syndrome pierre robin", "Pierre-Robin syndrome", "Pierre-Robin Syndrome", "Pierre Robin syndrome", "syndrome, Pierre Robin", "Sequence, Pierre Robin", "pierre robins syndrome", "sequence, Pierre Robin", "Pierre-robin deformity", "Robin syndrome, Pierre", "syndrome, Pierre-Robin", "Pierre Robins sequence", "Robin Syndrome, Pierre", "Pierre Robins Sequence", "Syndrome, Pierre-Robin", "Syndrome, Pierre Robin", "pierre robin's syndrome", "Pierre Robin's sequence", "Pierre Robin's Sequence", "Pierre Robin's syndrome", "Sequence, Pierre Robin's", "Pierre Robin association", "sequence, Pierre Robin's", "Pierre-robin malformation", "Robin sequence (disorder)", "Isolated Pierre Robin sequence", "isolated Pierre-Robin syndrome", "isolated Pierre Robin syndrome", "Isolated Pierre Robin syndrome", "isolated Pierre Robin sequence", "Pierre Robin syndrome (diagnosis)", "Micrognathia-glossoptosis syndrome", "syndrome; micrognathia-glossoptosis", "micrognathia-glossoptosis; syndrome", "Glossoptosis, Micrognathia, and Cleft Palate", "GLOSSOPTOSIS, MICROGNATHIA, AND CLEFT PALATE", "glossoptosis, micrognathia, and cleft palate", "Pierre Robin syndrome skeletal dysplasia polydactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated Pierre-Robin syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C5556294", "names": ["Metastatic Microsatellite Stable Endometrial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Microsatellite Stable Endometrial Carcinoma", "shortest_name_length": 54}
{"curie": "UMLS:C0275665", "names": ["Rectal gonorrhea", "rectal gonorrhea", "Rectal gonorrhoea", "gonococcal; rectum", "rectum; gonococcal", "Gonorrhea of rectum", "Gonococcal Proctitis", "gonococcal proctitis", "Gonorrhoea of rectum", "Gonococcal proctitis", "Proctitis gonococcal", "gonococcal; proctitis", "proctitis; gonococcal", "Gonorrhea of rectum (disorder)", "gonococcal proctitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gonorrhea of rectum", "shortest_name_length": 16}
{"curie": "MONDO:0009241", "names": ["Fountain syndrome", "fountain syndrome", "FOUNTAIN SYNDROME", "deafness, skeletal dysplasia, lip granuloma", "Deafness-skeletal dysplasia-lip granuloma syndrome", "deafness-skeletal dysplasia-lip granuloma syndrome", "Hearing loss-skeletal dysplasia-lip granuloma syndrome", "deafness with skeletal dysplasia and lip granuloma syndrome", "Deafness with skeletal dysplasia and lip granuloma syndrome", "deafness-skeletal dysplasia-coarse face with full lips syndrome", "Deafness-skeletal dysplasia-coarse face with full lips syndrome", "Deafness, skeletal dysplasia, coarse face with full lips syndrome", "Hearing loss-skeletal dysplasia-coarse face with full lips syndrome", "Deafness with skeletal dysplasia and lip granuloma syndrome (disorder)", "deafness with skeletal dysplasia and lip granuloma syndrome (diagnosis)", "Mental retardation-deafnes, skeletal abnormalities, coarse face with full lips", "intellectual disability, deafness, skeletal abnormalities, coarse face with full lips", "MENTAL RETARDATION, SENSORINEURAL DEAFNESS, SKELETAL ABNORMALITIES, AND COARSE FACE WITH FULL LIPS", "Mental Retardation, Sensorineural Deafness, Skeletal Abnormalities, And Coarse Face With Full Lips", "mental retardation, sensorineural deafness, skeletal abnormalities, and coarse face with full lips", "intellectual disability, sensorineural deafness, skeletal abnormalities, and coarse face with full lips"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fountain syndrome", "shortest_name_length": 17}
{"curie": "UMLS:C0086240", "names": ["Epilepsy, Simple Partial", "Simple Partial Epilepsies", "Partial Epilepsies, Simple", "Epilepsies, Simple Partial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epilepsy, Simple Partial", "shortest_name_length": 24}
{"curie": "UMLS:C0279641", "names": ["Childhood APL", "pediatric APL", "Pediatric APL", "childhood APL", "APL, childhood", "APL, pediatric", "Childhood APML", "M3 childhood APL", "Pediatric M3 APL", "Childhood M3 APL", "APL with PML-RARA", "pediatric acute M3 leukemia", "childhood acute M3 leukemia", "Childhood Acute M3 Leukemia", "Pediatric Acute M3 Leukemia", "M3 leukemia, childhood acute", "Pediatric Acute Promyelocytic Leukemia", "pediatric acute promyelocytic leukemia", "Childhood Acute Promyelocytic Leukemia", "promyelocytic leukemia, childhood acute", "leukemia, childhood acute promyelocytic", "acute promyelocytic leukemia, childhood", "Pediatric Acute Progranulocytic Leukemia", "pediatric acute progranulocytic leukemia", "childhood acute progranulocytic leukemia", "Childhood Acute Progranulocytic Leukemia", "M3 Pediatric Acute Promyelocytic Leukemia", "acute progranulocytic leukemia, childhood", "M3 pediatric acute promyelocytic leukemia", "progranulocytic leukemia, childhood acute", "M3 Childhood Acute Promyelocytic Leukemia", "M3 childhood acute promyelocytic leukemia", "Acute Promyelocytic Leukemia with PML-RARA", "Childhood Acute Promyelocytic Leukemia (M3)", "childhood acute promyelocytic leukemia (M3)", "Childhood APL with t(15;17)(q22;q12); PML-RARA", "Childhood APML with t(15;17)(q22;q12); PML-RARA", "Childhood Acute Promyelocytic Leukemia with PML-RARA", "Childhood Acute Promyelocytic Leukemia with t(15;17)(q22;q12); PML-RARA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Acute Promyelocytic Leukemia with PML-RARA", "shortest_name_length": 13}
{"curie": "MONDO:0006546", "names": ["Erythematosquamous Dermatosis", "erythematosquamous dermatosis", "Erythematosquamous dermatosis", "Erythematosquamous dermatosis, NOS", "Other erythematosquamous dermatosis", "Erythematosquamous dermatosis (disorder)", "erythematosquamous dermatosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythematosquamous dermatosis", "shortest_name_length": 29}
{"curie": "UMLS:C2747852", "names": ["Device related sepsis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Device related sepsis", "shortest_name_length": 21}
{"curie": "UMLS:C1336392", "names": ["Stage IVC Hypopharynx Carcinoma", "stage IVC hypopharyngeal cancer", "Stage IVC Hypopharyngeal Carcinoma", "Stage IVC Carcinoma of Hypopharynx", "Stage IVC Carcinoma of the Hypopharynx", "Stage IVC Hypopharyngeal Throat Cancer", "Stage IVC Hypopharyngeal Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Hypopharyngeal Carcinoma AJCC v7", "shortest_name_length": 31}
{"curie": "MONDO:0011513", "names": ["ALZHEIMER DISEASE, FAMILIAL EARLY-ONSET, WITH COEXISTING AMYLOID AND PRION PATHOLOGY", "Alzheimer disease, familial early-onset, with coexisting amyloid and prion pathology", "Alzheimer Disease, Familial Early-Onset, With Coexisting Amyloid And Prion Pathology"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alzheimer disease, familial early-onset, with coexisting amyloid and prion pathology", "shortest_name_length": 84}
{"curie": "UMLS:C1333955", "names": ["CNS Hemangioblastoma", "CNS hemangioblastoma", "hemangioblastoma of CNS", "Hemangioblastoma of CNS", "Hemangioblastoma of the CNS", "hemangioblastoma of the CNS", "central nervous system hemangioblastoma", "Central Nervous System Hemangioblastoma", "hemangioblastoma of central nervous system", "Hemangioblastoma of Central Nervous System", "Central Nervous System Capillary Hemangioblastoma", "central nervous system capillary hemangioblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Hemangioblastoma", "shortest_name_length": 20}
{"curie": "UMLS:C1696574", "names": ["Application site erosion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Application site erosion", "shortest_name_length": 24}
{"curie": "UMLS:C4528759", "names": ["IIIA", "Stage IIIA Intrahepatic Cholangiocarcinoma AJCC v8", "Stage IIIA Intrahepatic Bile Duct Cancer (Cholangiocarcinoma)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Intrahepatic Cholangiocarcinoma AJCC v8", "shortest_name_length": 4}
{"curie": "UMLS:C1880083", "names": ["Cigarette Smoking Toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cigarette Smoking Toxicity", "shortest_name_length": 26}
{"curie": "MONDO:0019994", "names": ["UPD(13)mat", "maternal uniparental disomy of chromosome 13", "maternal uniparental disomy of chromosome type 13"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maternal uniparental disomy of chromosome 13", "shortest_name_length": 10}
{"curie": "MONDO:0035452", "names": ["Brailsford disease", "mueller-weiss syndrome", "Mueller-Weiss osteonecrosis of the tarsal bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mueller-weiss syndrome", "shortest_name_length": 18}
{"curie": "UMLS:C3897511", "names": ["Stage IVB Thyroid Gland Papillary Cancer", "Stage IVB Thyroid Gland Papillary Carcinoma", "Stage IVB Thyroid Gland Papillary Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Thyroid Gland Papillary Carcinoma AJCC v7", "shortest_name_length": 40}
{"curie": "UMLS:C4049489", "names": ["Thoracic Endometriosis", "Thoracic endometriosis", "endometriosis thoracic", "Endometriosis of thorax", "Endometriosis of thorax (disorder)", "Thoracic endometriosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endometriosis of thorax", "shortest_name_length": 22}
{"curie": "MONDO:0020144", "names": ["cerebrovascular dementia", "rare cerebrovascular dementia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebrovascular dementia", "shortest_name_length": 24}
{"curie": "MONDO:0011445", "names": ["SPG11", "HSP-TCC", "Hsp-Tcc", "spastic paraplegia 11", "Spastic Paraplegia 11", "Nakamura Osame syndrome", "Nakamura-Osame syndrome", "Spastic Paraplegia Type 11", "hereditary spastic paraplegia 11", "SPG11 hereditary spastic paraplegia", "hereditary spastic paraplegia type 11", "autosomal recessive spastic paraplegia 11", "Spastic paraplegia 11, autosomal recessive", "spastic paraplegia 11, autosomal recessive", "SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE", "Autosomal recessive spastic paraplegia type 11", "autosomal recessive spastic paraplegia type 11", "familial spastic paraplegia autosomal recessive type 11", "hereditary spastic paraplegia caused by mutation in SPG11", "Autosomal recessive spastic paraplegia type 11 (disorder)", "Autosomal recessive spastic paraplegia type 11 (diagnosis)", "Spastic paraplegia, mental retardation and thin corpus callosum", "spastic paraplegia - intellectual deficit - thin corpus callosum", "Spastic paraplegia, intellectual disability and thin corpus callosum", "Spg11-Related Hereditary Spastic Paraplegia with Thin Corpus Callosum", "Spastic paraplegia-intellectual disability-thin corpus callosum syndrome", "spastic paraplegia-intellectual disability-thin corpus callosum syndrome", "hereditary spastic paraplegia mental impairment and thin corpus callosum", "Autosomal Recessive Spastic Paraplegia Complicated with Thin Corpus Callosum", "autosomal recessive spastic paraplegia complicated with thin corpus callosum", "SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUS CALLOSUM", "spastic paraplegia, autosomal recessive, complicated, with thin corpus callosum", "Spastic Paraplegia, Autosomal Recessive, Complicated, with Thin Corpus Callosum", "autosomal recessive spastic paraplegia with mental impairment and thin corpus callosum", "Autosomal Recessive Spastic Paraplegia with Mental Impairment and Thin Corpus Callosum", "SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT AND THIN CORPUS CALLOSUM", "Spastic Paraplegia, Autosomal Recessive, with Mental Impairment and Thin Corpus Callosum", "spastic paraplegia, autosomal recessive, with mental impairment and thin corpus callosum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 11", "shortest_name_length": 5}
{"curie": "MONDO:0019942", "names": ["Distal arthrogryposis", "distal arthrogryposis", "Arthrogryposis, distal", "distal arthrogryposis syndrome", "Distal arthrogryposis syndrome", "Arthrogryposis Multiplex Congenita", "Distal arthrogryposis syndrome (disorder)", "arthrogryposis multiplex congenita distal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal arthrogryposis", "shortest_name_length": 21}
{"curie": "UMLS:C1335123", "names": ["Oral Cavity Pleomorphic Adenoma", "Pleomorphic Adenoma of Oral Cavity", "Pleomorphic Adenoma of the Oral Cavity", "Benign Mixed Salivary Tumor of Oral Cavity", "Benign Mixed Salivary Tumor of the Oral Cavity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral Cavity Pleomorphic Adenoma", "shortest_name_length": 31}
{"curie": "MONDO:0009158", "names": ["EDS X", "EDS10", "EDS 10", "FN ABNORMALITY", "FN Abnormality", "EDS10 (formerly)", "Ehlers-Danlos Syndrome, Type X", "EHLERS-DANLOS SYNDROME, TYPE X", "Ehlers-Danlos syndrome type 10", "Ehlers-Danlos syndrome, type 10", "Ehlers-Danlos syndrome type 10 (formerly)", "Ehlers-Danlos syndrome, type X (formerly)", "Ehlers-Danlos syndrome, dysfibronectinemic", "Ehlers-Danlos syndrome, dysfibronectinaemic", "Ehlers-Danlos syndrome, fibronectinemic type", "Ehlers-Danlos syndrome, fibronectin-deficient", "Ehlers-Danlos syndrome dysfibronectinemic type", "Ehlers-Danlos Syndrome, Dysfibronectinemic Type", "Ehlers-Danlos syndrome, dysfibronectinemic type", "EHLERS-DANLOS SYNDROME, DYSFIBRONECTINEMIC TYPE", "Ehlers-Danlos syndrome with platelet dysfunction", "Ehlers-Danlos syndrome, dysfibronectinemic (disorder)", "Ehlers-Danlos syndrome, dysfibronectinemic type (diagnosis)", "EHLERS-DANLOS SYNDROME WITH PLATELET DYSFUNCTION FROM FIBRONECTIN ABNORMALITY", "Ehlers-Danlos syndrome with platelet dysfunction from fibronectin abnormality", "Ehlers-Danlos Syndrome with Platelet Dysfunction from Fibronectin Abnormality"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ehlers-Danlos syndrome, fibronectinemic type", "shortest_name_length": 5}
{"curie": "UMLS:C0152966", "names": ["pneumococcemia", "Pneumococcal sepsis", "pneumococcal sepsis", "sepsis; pneumococcal", "pneumococcal; sepsis", "pneumococcal septicemia", "Pneumococcal septicemia", "Pneumococcal septicaemia", "pneumococcemia (diagnosis)", "Streptococcus pneumoniae septicemia", "pneumococcal septicemia (diagnosis)", "Streptococcus pneumoniae septicaemia", "Septicemia due to Streptococcus pneumoniae", "Septicaemia due to Streptococcus pneumoniae", "streptoccocal; sepsis, Streptococcus pneumoniae", "sepsis; streptococcal, streptoccocal, pneumoniae", "Pneumococcal septicemia [Streptococcus pneumoniae septicemia]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pneumococcal sepsis", "shortest_name_length": 14}
{"curie": "UMLS:C1519370", "names": ["Anaplastic Large Cell Lymphoma, Signet Ring-Like Subtype"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anaplastic Large Cell Lymphoma, Signet Ring-Like Subtype", "shortest_name_length": 56}
{"curie": "MONDO:0004472", "names": ["blunt duct adenosis of breast", "Columnar Cell Change of the Breast", "breast columnar cell mucinous carcinoma", "Breast Columnar Cell Mucinous Carcinoma", "Breast Columnar Cell Mucinous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast columnar cell mucinous carcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0018673", "names": ["IgG4-related pachymeningitis", "idiopathic hypertrophic pachymeningitis", "Idiopathic hypertrophic pachymeningitis", "Immunoglobulin G4 related pachymeningitis", "idiopathic hypertrophic spinal pachymeningitis", "idiopathic hypertrophic cranial pachymeningitis", "Immunoglobulin G4 related pachymeningitis (disorder)", "idiopathic hypertrophic craniospinal pachymeningitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IgG4-related pachymeningitis", "shortest_name_length": 28}
{"curie": "UMLS:C4553695", "names": ["IVB", "Stage IVB Cervical Cancer", "Stage IVB Cervical Cancer AJCC v8", "Stage IVB Cervical Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Cervical Cancer AJCC v8", "shortest_name_length": 3}
{"curie": "MONDO:0004334", "names": ["NF-PanNET", "Non-functioning PNET", "non-functioning EPTs", "non-functioning PNET", "non-syndromic pancreatic NET", "Non-Syndromic Pancreatic NET", "nonfunctional pancreatic NET", "Nonfunctional Pancreatic NET", "non-functioning pancreatic NET", "Non-Functioning Pancreatic NET", "Non-functioning pancreatic NET", "Inactive Pancreatic Endocrine Tumor", "inactive pancreatic endocrine tumor", "Nonsyndromic Pancreatic Endocrine Tumor", "nonsyndromic pancreatic endocrine tumor", "non-functioning pancreatic endocrine tumor", "Pancreatic endocrine tumor, nonfunctioning", "non functioning pancreatic endocrine tumor", "Non-Functioning Pancreatic Endocrine Tumor", "Non functioning pancreatic endocrine tumor", "non-functioning endocrine pancreatic tumors", "Non-functioning endocrine pancreatic tumors", "Pancreatic endocrine tumour, nonfunctioning", "nonsyndromic pancreatic neuroendocrine tumor", "Nonsyndromic Pancreatic Neuroendocrine Tumor", "Non-Syndromic Pancreatic Neuroendocrine Tumor", "nonfunctional pancreatic neuroendocrine tumor", "non-syndromic pancreatic neuroendocrine tumor", "Nonfunctional Pancreatic Neuroendocrine Tumor", "non-functional pancreatic neuroendocrine tumor", "Non-Functional Pancreatic Neuroendocrine Tumor", "Nonfunctioning Pancreatic Neuroendocrine Tumor", "non-functioning pancreatic neuroendocrine tumor", "Non-functioning pancreatic neuroendocrine tumor", "Pancreatic neuroendocrine tumor, nonfunctioning", "Non-Functioning Pancreatic Neuroendocrine Tumor", "Non-functioning neuroendocrine tumor of pancreas", "non-functioning neuroendocrine tumor of pancreas", "Pancreatic neuroendocrine tumour, nonfunctioning", "non-functioning well-differentiated pancreatic NEN", "Non-functioning well-differentiated pancreatic NEN", "Pancreatic neuroendocrine neoplasm, non-functioning", "Non-functioning well-differentiated NEN of pancreas", "Non-functioning neuroendocrine neoplasm of pancreas", "non-functioning well-differentiated NEN of pancreas", "Non-functioning PNET (pancreatic neuroendocrine tumor)", "Non-functioning PNET (pancreatic neuroendocrine tumour)", "Non-functioning neuroendocrine neoplasm of pancreas (disorder)", "non-functioning well differentiated pancreatic endocrine tumor", "Non-Functioning Well Differentiated Pancreatic Endocrine Tumor", "Pancreatic endocrine tumor, nonfunctioning (morphologic abnormality)", "Non-functioning well-differentiated pancreatic neuroendocrine neoplasm", "non-functioning well-differentiated pancreatic neuroendocrine neoplasm", "Non-functioning well-differentiated neuroendocrine neoplasm of pancreas", "non-functioning well-differentiated neuroendocrine neoplasm of pancreas", "Non-functioning well-differentiated pancreatic NEN (neuroendocrine neoplasm)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-functional pancreatic neuroendocrine tumor", "shortest_name_length": 9}
{"curie": "MONDO:0013247", "names": ["FRTS2", "SLC34A1 Fanconi syndrome", "FANCONI RENOTUBULAR SYNDROME 2", "Fanconi renotubular syndrome 2", "Fanconi renotubular syndrome type 2", "Fanconi syndrome caused by mutation in SLC34A1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fanconi renotubular syndrome 2", "shortest_name_length": 5}
{"curie": "MONDO:0008408", "names": ["SPSMA", "scapuloperoneal neuronopathy", "scapuloperoneal spinal muscular atrophy", "Scapuloperoneal spinal muscular atrophy", "neurogenic scapuloperoneal amyotrophy, New England type", "amyotrophy, neurogenic scapuloperoneal, New England type", "scapuloperoneal spinal muscular atrophy, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scapuloperoneal spinal muscular atrophy, autosomal dominant", "shortest_name_length": 5}
{"curie": "MONDO:0008816", "names": ["Cm2", "CM2", "Arnold Chiari type 2", "Chiari malformation type 2", "Chiari Malformation Type 2", "Arnold-Chiari malformation", "Chiari type II malformation", "Chiari Malformation Type II", "type II Chiari malformation", "Chiari malformation type II", "CHIARI MALFORMATION TYPE II", "Chiari malformation, type II", "Arnold-Chiari syndrome, type II", "Arnold-Chiari malformation type 2", "Type II Arnold Chiari malformation", "type II Arnold-Chiari malformation", "Arnold-Chiari Malformation, Type 2", "Type II Arnold Chiari Malformation", "Type II Arnold-Chiari Malformation", "Arnold Chiari malformation type II", "Arnold-Chiari type II malformation", "Arnold-Chiari malformation type II", "Arnold Chiari Malformation, Type 2", "Arnold-Chiari Malformation, Type II", "Arnold Chiari Malformation, Type II", "Chiari malformation type II (disorder)", "type II Chiari malformation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chiari malformation type II", "shortest_name_length": 3}
{"curie": "MONDO:0000866", "names": ["myoglobinuria", "Myoglobinuria", "MYOGLOBINURIA", "myoglobinurias", "Myoglobinurias", "myoglobulinuria", "Myoglobinuria (finding)", "hereditary myoglobinuria", "myoglobinuria (diagnosis)", "Urine myoglobin increased", "Myoglobin urine increased"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary myoglobinuria", "shortest_name_length": 13}
{"curie": "MONDO:0010051", "names": ["spastic quadriplegia retinitis pigmentosa mental retardation", "spastic quadriplegia retinitis pigmentosa intellectual disability", "Spastic Quadriplegia, Retinitis Pigmentosa, and Mental Retardation", "SPASTIC QUADRIPLEGIA, RETINITIS PIGMENTOSA, AND MENTAL RETARDATION", "spastic quadriplegia, retinitis pigmentosa, and mental retardation", "spastic quadriplegia-retinitis pigmentosa-mental retardation syndrome", "spastic quadriplegia, retinitis pigmentosa, and intellectual disability", "spastic tetraplegia-retinitis pigmentosa-intellectual disability syndrome", "spastic quadriplegia-retinitis pigmentosa-intellectual disability syndrome", "progressive quadriparesis, mental retardation, retinitis pigmentosa and hearing loss", "progressive quadriparesis, intellectual disability, retinitis pigmentosa and hearing loss"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic tetraplegia-retinitis pigmentosa-intellectual disability syndrome", "shortest_name_length": 60}
{"curie": "MONDO:0019670", "names": ["Manus valga", "Ulnar clubhand", "ulnar clubhand", "ulnar hemimelia", "Manus valga (disorder)", "ulnar longitudinal meromelia", "congenital longitudinal deficiency of the ulna"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ulnar hemimelia", "shortest_name_length": 11}
{"curie": "MONDO:0002622", "names": ["Multifocal osteosarcoma", "multifocal osteosarcoma", "Multifocal Osteosarcoma", "Multicentric osteosarcoma", "multicentric osteosarcoma", "Multicentric Osteosarcoma", "Multifocal Osteogenic Sarcoma", "multifocal osteogenic sarcoma", "Multifocal osteosarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multifocal osteogenic sarcoma", "shortest_name_length": 23}
{"curie": "UMLS:C5238349", "names": ["Recurrent NMIBC with a Prior History of Low or Intermediate Risk NMIBC", "Recurrent Non-Muscle Invasive Bladder Urothelial Carcinoma (NMIBC) with a Prior History of Low or Intermediate Risk NMIBC", "Recurrent Non-Muscle Invasive Bladder Urothelial Carcinoma with a Prior History of Low or Intermediate Risk Non-Muscle Invasive Bladder Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Non-Muscle Invasive Bladder Urothelial Carcinoma (NMIBC) with a Prior History of Low or Intermediate Risk NMIBC", "shortest_name_length": 70}
{"curie": "MONDO:0012108", "names": ["SEMDBCD", "SEMD MATN3-related", "SEMD, MATN3-RELATED", "SEMD, MATN3-related", "SEMD, matrilin-3 type", "spondyloepimetaphyseal dysplasia matrilin-3 type", "Spondyloepimetaphyseal dysplasia matrilin-3 type", "Spondyloepimetaphyseal dysplasia, matrilin-3 type", "spondyloepimetaphyseal dysplasia, matrilin-3 type", "spondyloepimetaphyseal dysplasia matrilin-3 related", "Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related", "spondyloepimetaphyseal dysplasia, matrilin-3 related", "SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MATRILIN-3 RELATED", "Spondyloepimetaphyseal dysplasia matrilin-3 type (disorder)", "SPONDYLOEPIMETAPHYSEAL DYSPLASIA, BOROCHOWITZ-CORMIER-DAIRE TYPE", "spondyloepimetaphyseal dysplasia, Borochowitz-Cormier-Daire type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepimetaphyseal dysplasia, matrilin-3 type", "shortest_name_length": 7}
{"curie": "MONDO:0044675", "names": ["LRP5-related primary osteoporosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "LRP5-related primary osteoporosis", "shortest_name_length": 33}
{"curie": "MONDO:0020093", "names": ["autosomal dominant isolated diffuse palmoplantar keratoderma", "isolated diffuse palmoplantar keratoderma, autosomal dominant", "autosomal dominant isolated diffuse palmoplantar hyperkeratosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant isolated diffuse palmoplantar keratoderma", "shortest_name_length": 60}
{"curie": "UMLS:C4054406", "names": ["Nephropathy due to Amphotericin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephropathy due to Amphotericin", "shortest_name_length": 31}
{"curie": "UMLS:C4763800", "names": ["Refractory Subcutaneous Panniculitis-Like T-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Subcutaneous Panniculitis-Like T-Cell Lymphoma", "shortest_name_length": 57}
{"curie": "MONDO:0013426", "names": ["LDS3", "LDS1C", "LDS1C, FORMERLY", "Loeys-Dietz syndrome 3", "LOEYS-DIETZ SYNDROME 3", "Loeys-Dietz syndrome type 3", "Loeys-Dietz Syndrome Type 3", "Loeys-Dietz syndrome type 1C", "Loeys-Dietz syndrome, type 3", "Loeys-Dietz syndrome, type 1C", "Aneurysm-osteoarthritis syndrome", "aneurysm-osteoarthritis syndrome", "Aneurysm osteoarthritis syndrome", "ANEURYSMS-OSTEOARTHRITIS SYNDROME", "aneurysms-osteoarthritis syndrome", "aneurysm - osteoarthritis syndrome", "Loeys-Dietz syndrome type 3 (diagnosis)", "LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY", "Loeys-Dietz syndrome, type 1C, formerly", "Loeys-Dietz syndrome with osteoarthritis", "Loeys-Dietz syndrome, type 1C (formerly)", "LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS", "Aneurysm osteoarthritis syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aneurysm-osteoarthritis syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0001134", "names": ["EHT", "primary hypertension", "hypertension primary", "Primary hypertension", "Primary Hypertension", "Hypertension, Primary", "Primary Hypertensions", "essential hypertension", "HYPERTENSION ESSENTIAL", "Essential Hypertension", "Hypertension;essential", "Essential hypertension", "Hypertensions, Primary", "Idiopathic hypertension", "idiopathic hypertension", "Hypertension, Essential", "HYPERTENSION, ESSENTIAL", "Primary hypertension, NOS", "Essential hypertension, NOS", "Essential (primary) hypertension", "Essential hypertension (disorder)", "essential hypertension unspecified", "HYPERTENSION, ARTERIAL, IDIOPATHIC", "essential hypertension (diagnosis)", "Unspecified essential hypertension", "Essential hypertension, unspecified", "Systemic primary arterial hypertension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "essential hypertension", "shortest_name_length": 3}
{"curie": "MONDO:0021021", "names": ["CDD", "Schaefer Stein Oshman syndrome", "craniodiaphyseal dysplasia, dominant", "autosomal dominant craniodiaphyseal dysplasia", "Craniodiaphyseal Dysplasia, Autosomal Dominant", "craniodiaphyseal dysplasia, autosomal dominant", "CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT", "dominantly inherited craniodiaphyseal dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniodiaphyseal dysplasia, autosomal dominant", "shortest_name_length": 3}
{"curie": "MONDO:0100046", "names": ["pseudoexfoliation syndrome", "pseudoexfoliation glaucoma", "pseudoexfoliation of the lens", "exfoliation syndrome, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exfoliation syndrome, susceptibility to", "shortest_name_length": 26}
{"curie": "UMLS:C1335256", "names": ["Stage 2 Hepatoblastoma", "PRETEXT Stage 2 Hepatoblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PRETEXT Stage 2 Hepatoblastoma", "shortest_name_length": 22}
{"curie": "UMLS:C4331343", "names": ["Stage IVB Major Salivary Gland Cancer", "Stage IVB Major Salivary Gland Cancer AJCC v8", "Stage IVB Major Salivary Gland Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Major Salivary Gland Cancer AJCC v8", "shortest_name_length": 37}
{"curie": "MONDO:0016490", "names": ["C-beta-thalassemia", "HBC-beta-thalassemia syndrome", "hemoglobin C-beta-thalassemia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemoglobin C-beta-thalassemia syndrome", "shortest_name_length": 18}
{"curie": "OMIM:614752", "names": ["IL6, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS", "INTERLEUKIN 6, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 45}
{"curie": "MONDO:0018646", "names": ["PSC", "Fibrous cholangitis", "fibrosing cholangitis", "sclerosing cholangitis", "Sclerosing cholangitis", "CHOLANGITIS, FIBROSING", "SCLEROSING CHOLANGITIS", "Sclerosing Cholangitis", "Cholangitis sclerosing", "CHOLANGITIS SCLEROSING", "Cholangitis, Sclerosing", "sclerosing cholangiitis", "Sclerosing Cholangiitis", "Cholangiitis, Sclerosing", "Sclerosing Cholangitides", "Cholangitides, Sclerosing", "Sclerosing Cholangiitides", "Cholangiitides, Sclerosing", "Primary Sclerosing Cholangitis", "Primary sclerosing cholangitis", "sclerosing cholangitis (disease)", "chronic obliterative cholangitis", "Sclerosing cholangitis (disorder)", "CHOLANGITIS, OBLITERATIVE, CHRONIC", "sclerosing cholangitis (diagnosis)", "primary sclerosing cholangitis (PSC)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sclerosing cholangitis", "shortest_name_length": 3}
{"curie": "UMLS:C0242381", "names": ["Lyme arthritis", "Lyme Arthritis", "lyme arthritis", "LYME ARTHRITIS", "Arthritis, Lyme", "lyme disease arthritis", "arthritis disease lymes", "Lyme arthritis (disorder)", "Arthritis in Lyme disease", "arthritis; Lyme disease (manifestation)", "Lyme disease; arthritis (manifestation)", "Arthritis in Lyme disease, site unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lyme Arthritis", "shortest_name_length": 14}
{"curie": "MONDO:0004386", "names": ["body of uterus atypical polypoid adenomyoma", "uterine corpus atypical polypoid adenomyoma", "Uterine Corpus Atypical Polypoid Adenomyoma", "atypical polypoid adenomyoma of body of uterus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine corpus atypical polypoid adenomyoma", "shortest_name_length": 43}
{"curie": "MONDO:0017863", "names": ["Digitalism", "digitalis poisoning", "Digitalis poisoning", "digitalis glycoside toxicity", "Poisoning by Digitalis glycoside", "Poisoning by digitalis glycosides", "toxicity from digitalis glycosides", "Poisoning by digitalis glycoside, NOS", "Poisoning caused by Digitalis glycoside", "digitalis glycoside toxicity (diagnosis)", "Poisoning caused by Digitalis glycoside (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "digitalis poisoning", "shortest_name_length": 10}
{"curie": "MONDO:0001503", "names": ["primary eye hypotony", "Primary hypotony of eye", "primary hypotony of eye", "Primary hypotony of eye (disorder)", "primary hypotony of eye (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary eye hypotony", "shortest_name_length": 20}
{"curie": "UMLS:C1558210", "names": ["Intraoperative injury", "Intraoperative Injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraoperative injury", "shortest_name_length": 21}
{"curie": "UMLS:C4524854", "names": ["Appendix Carcinoma by AJCC v7 Stage", "Appendiceal Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Appendix Carcinoma by AJCC v7 Stage", "shortest_name_length": 35}
{"curie": "MONDO:0006636", "names": ["Actinobacillus Infection", "Actinobacillus infection", "Actinobacillus Infections", "Infection, Actinobacillus", "infection; Actinobacillus", "Actinobacillus; infection", "ACTINOBACILLUS INFECTIONS", "infection, Actinobacillus", "infections, Actinobacillus", "Infections, Actinobacillus", "Actinobacillus infection, NOS", "Actinobacillus infectious disease", "Actinobacillus disease or disorder", "Actinobacillus infection (disorder)", "Actinobacillus caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Actinobacillus infectious disease", "shortest_name_length": 24}
{"curie": "MONDO:0030971", "names": ["IMD78", "TPP2 DEFICIENCY", "TPP2 deficiency", "TRIANGLE disease", "TPPII deficiency", "Tripeptidyl-peptidase II deficiency", "TPPII (tripeptidyl-peptidase II) deficiency", "Evans syndrome associated with primary immunodeficiency", "IMMUNODEFICIENCY 78 WITH AUTOIMMUNITY AND DEVELOPMENTAL DELAY", "immunodeficiency 78 with autoimmunity and developmental delay", "Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome", "Autoimmune hemolytic anemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome", "Autoimmune haemolytic anaemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome", "Autoimmune hemolytic anemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome (disorder)", "TPPII-related immunodeficiency, autoimmunity and neurodevelopmental delay with impaired glycolysis and lysosomal expansion disease", "TRIANGLE (TPPII-related immunodeficiency, autoimmunity, neurodevelopmental delay, impaired glycolysis, lysosomal expansion) disease", "TPPII-related immunodeficiency, autoimmunity, and neurodevelopmental delay with impaired glycolysis and lysosomal expansion disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 78 with autoimmunity and developmental delay", "shortest_name_length": 5}
{"curie": "UMLS:C4727360", "names": ["Recurrent Submandibular Gland Acinic Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Submandibular Gland Acinic Cell Carcinoma", "shortest_name_length": 51}
{"curie": "MONDO:0009101", "names": ["Wfs", "WFS1", "DIDMOAD", "WOLFRAM SYNDROME 1", "Wolfram Syndrome 1", "WOLFRAM syndrome 1", "Wolfram syndrome 1", "WFS1 Wolfram syndrome", "Wolfram syndrome type 1", "Wolfram syndrome caused by mutation in WFS1", "diabetes mellitus AND insipidus with optic atrophy AND deafness", "diabetes insipidus and mellitus with optic atrophy and deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wolfram syndrome 1", "shortest_name_length": 3}
{"curie": "MONDO:0008041", "names": ["myoclonic epilepsy, Hartung type", "Myoclonic Epilepsy, Hartung Type", "MYOCLONIC EPILEPSY, HARTUNG TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myoclonic epilepsy, Hartung type", "shortest_name_length": 32}
{"curie": "UMLS:C5447327", "names": ["SCID-PTPRC", "CD45 Deficiency", "Severe Combined Immunodeficiency due to CD45 Deficiency", "Severe Combined Immunodeficiency, T cell-Negative, B-cell/Natural Killer Cell Positive, PTPRC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Severe Combined Immunodeficiency due to CD45 Deficiency", "shortest_name_length": 10}
{"curie": "UMLS:C5420171", "names": ["Nasopharyngeal Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasopharyngeal Non-Hodgkin Lymphoma", "shortest_name_length": 35}
{"curie": "UMLS:C1739148", "names": ["Acute Synovitis", "Acute synovitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute synovitis", "shortest_name_length": 15}
{"curie": "MONDO:0030261", "names": ["PCH1F", "pontocerebellar hypoplasia type 1F", "PONTOCEREBELLAR HYPOPLASIA, TYPE 1F", "pontocerebellar hypoplasia, type 1F"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pontocerebellar hypoplasia, type 1F", "shortest_name_length": 5}
{"curie": "MONDO:0006962", "names": ["Seba", "Sebaceous Cancer", "sebaceous cancer", "sebaceous carcinoma", "Sebaceous Carcinoma", "Sebaceous carcinoma", "adenocarcinoma sebaceous", "sebaceous adenocarcinoma", "Sebaceous adenocarcinoma", "Sebaceous Adenocarcinoma", "Sebaceous Gland Carcinoma", "Adenocarcinoma, Sebaceous", "Carcinoma, Sebaceous Cell", "Sebaceous Adenocarcinomas", "sebaceous gland carcinoma", "malignant sebaceous tumor", "malignant Sebaceous tumor", "Sebaceous gland carcinoma", "Adenocarcinomas, Sebaceous", "[M]Sebaceous adenocarcinoma", "Carcinoma of Sebaceous Gland", "carcinoma of sebaceous gland", "Carcinoma of sebaceous gland", "Malignant Sebaceous Neoplasm", "Sebaceous gland adenocarcinoma", "sebaceous gland adenocarcinoma", "carcinoma of the sebaceous gland", "Carcinoma of the Sebaceous Gland", "malignant sebaceous adenocarcinoma", "Sebaceous adenocarcinoma (disorder)", "adenocarcinoma, sebaceous, malignant", "ADENOCARCINOMA, SEBACEOUS, MALIGNANT", "sebaceous adenocarcinoma (diagnosis)", "adenocarcinoma of the sebaceous gland", "malignant neoplasm of sebaceous gland", "adenocarcinoma of the Sebaceous gland", "Sebaceous adenocarcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sebaceous adenocarcinoma", "shortest_name_length": 4}
{"curie": "UMLS:C1333980", "names": ["Hepatobiliary Precancerous Condition", "Hepato-Biliary Precancerous Condition", "Hepato-Biliary Premalignant Condition", "Liver and Biliary Precancerous Condition", "Liver and Biliary System Precancerous Condition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatobiliary Precancerous Condition", "shortest_name_length": 36}
{"curie": "UMLS:C1335489", "names": ["Breast Non-Hodgkin Lymphoma", "Non-Hodgkin Breast Lymphoma", "Non-Hodgkin's Breast Lymphoma", "non-Hodgkin's lymphoma of breast", "Primary Non-Hodgkin Breast Lymphoma", "Primary Non-Hodgkin's Breast Lymphoma", "Primary Non-Hodgkin Lymphoma of Breast", "Primary Non-Hodgkin's Lymphoma of Breast", "malignant lymphoma of breast (diagnosis)", "Primary Non-Hodgkin Lymphoma of the Breast", "non-Hodgkin's lymphoma of breast (diagnosis)", "Primary Non-Hodgkin's Lymphoma of the Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Hodgkin Breast Lymphoma", "shortest_name_length": 27}
{"curie": "UMLS:C3897219", "names": ["Untreated Subependymal Giant Cell Astrocytoma", "untreated childhood subependymal giant cell astrocytoma", "Untreated Childhood Subependymal Giant Cell Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Untreated Childhood Subependymal Giant Cell Astrocytoma", "shortest_name_length": 45}
{"curie": "MONDO:0020633", "names": ["anaplastic cancer", "Anaplastic Malignant Neoplasm", "anaplastic malignant neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anaplastic cancer", "shortest_name_length": 17}
{"curie": "UMLS:C5231189", "names": ["Vagus Nerve Palsy", "Palsy of vagus nerve", "Cranial Nerve X Palsy", "Cranial nerve palsy X", "Tenth cranial nerve palsy", "Tenth Cranial Nerve Palsy", "Palsy of vagus nerve (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Palsy of vagus nerve", "shortest_name_length": 17}
{"curie": "UMLS:C0235842", "names": ["Deciduitis", "DECIDUITIS", "Decidual endometritis", "Endometritis decidual", "endometritis decidual", "ENDOMETRITIS DECIDUAL", "ENDOMETRITIS, DECIDUAL", "Decidual endometritis (disorder)", "Decidual endometritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Decidual endometritis", "shortest_name_length": 10}
{"curie": "UMLS:C4289810", "names": ["Cervical Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Neuroendocrine Neoplasm", "shortest_name_length": 32}
{"curie": "UMLS:C0281778", "names": ["Anal abscess", "ANAL ABSCESS", "Abscess;anal", "abscess anal", "anal abscess", "Anal Abscess", "abscesses anal", "Anal abscess (disorder)", "anal abscess (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anal abscess", "shortest_name_length": 12}
{"curie": "MONDO:0019945", "names": ["solar urticaria", "Urticaria light", "Solar urticaria", "Light urticaria", "Solar Urticaria", "SOLAR URTICARIA", "Urticaria, Solar", "urticaria; solar", "solar; urticaria", "sunshine; urticaria", "urticaria; sunshine", "Photogenic urticaria", "Solar urticaria, NOS", "Photosensitivity urticaria", "Solar urticaria (disorder)", "solar urticaria (diagnosis)", "Sunlight-induced angioedema-urticaria", "Sunlight-induced angio-edema-urticaria", "Sunlight-induced angio-oedema-urticaria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "solar urticaria", "shortest_name_length": 15}
{"curie": "MONDO:0035423", "names": ["TGCV", "triglyceride deposit cardiomyovasculopathy", "Neutral lipid storage disease with severe cardiovascular involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "triglyceride deposit cardiomyovasculopathy", "shortest_name_length": 4}
{"curie": "UMLS:C0751555", "names": ["Post-Traumatic Tic Disorder", "Post Traumatic Tic Disorder", "Post-Traumatic Tic Disorders", "Tic Disorder, Post-Traumatic", "Tic Disorder, Post Traumatic", "Tic Disorders, Post-Traumatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post-Traumatic Tic Disorder", "shortest_name_length": 27}
{"curie": "MONDO:0010707", "names": ["Paine syndrome", "PAINE SYNDROME", "Seemanova Syndrome I", "Seemanova syndrome 1", "SEEMANOVA SYNDROME I", "Microcephaly with spastic diplegia", "MICROCEPHALY WITH SPASTIC DIPLEGIA", "microcephaly with spastic diplegia", "microcephaly-spastic diplegia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paine syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0004670", "names": ["lupus", "Lupus", "Lupus erythematosus", "lupus erythematosus", "Lupus Erythematosus", "erythematosus; lupus", "lupus; erythematosus", "Lupus erythematosus NOS", "LE - Lupus erythematosus", "Lupus erythematosus (disorder)", "Lupus erythematosus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lupus erythematosus", "shortest_name_length": 5}
{"curie": "MONDO:0020448", "names": ["right IVC connecting to left-sided atrium", "right inferior vena cava connecting to left-sided atrium", "right inferior caval vein connecting to left-sided atrium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "right inferior vena cava connecting to left-sided atrium", "shortest_name_length": 41}
{"curie": "MONDO:0005668", "names": ["fancier's lung", "bird fancier lung", "Bird Fancier Lung", "fancier's disease", "Bird fancier lung", "Bird Fanciers Lung", "bird fanciers lung", "bird breeders lung", "Bird fanciers lung", "bird breeder's lung", "Bird-fanciers' lung", "Bird fanciers' lung", "bird-fanciers' lung", "Bird Fancier's Lung", "Bird breeders' lung", "bird-breeder's lung", "Bird fancier's lung", "Bird-Breeder's Lung", "bird fancier's lung", "Bird-fancier's lung", "bird-fancier's lung", "BIRD BREEDER DISEASE", "Lung, Bird Fancier's", "Bird Fancier's Lungs", "bird fancier disease", "pigeon breeder's lung", "bird disease fanciers", "Pigeon-Breeder's Lung", "pigeon-breeder's lung", "poultry worker's lung", "Lungs, Bird Fancier's", "Pigeon fancier's lung", "bird fanciers' disease", "Bird fanciers' disease", "bird-fanciers' disease", "Bird breeders' disease", "bird fancier's; disease", "BFL - Bird fanciers lung", "Bird-fanciers' lung, NOS", "Pigeon-breeders's disease", "pigeon fancier's; disease", "Pigeon-breeder lung disease", "pigeon-breeder lung disease", "Bird-fanciers' lung (disorder)", "bird fancier's disease or lung", "Avian protein hypersensitivity", "Avian hypersensitivity Pneumonitis", "Avian Hypersensitivity Pneumonitis", "Avian hypersensitivity pneumonitis", "bird-fanciers' disease (diagnosis)", "Hypersensitivity Pneumonitis, Avian", "Pneumonitis, Avian Hypersensitivity", "Pneumonitis, Hypersensitivity, Avian", "Avian Hypersensitivity Pneumonitides", "Pneumonitides, Avian Hypersensitivity", "Hypersensitivity Pneumonitides, Avian", "disease (or disorder); bird fancier's"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bird fancier's lung", "shortest_name_length": 14}
{"curie": "UMLS:C4683686", "names": ["Adult T-Cell Leukemia/Lymphoma by Ann Arbor Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult T-Cell Leukemia/Lymphoma by Ann Arbor Stage", "shortest_name_length": 49}
{"curie": "UMLS:C1332502", "names": ["Benign Gallbladder Granular Cell Tumor", "Gallbladder Benign Granular Cell Tumor", "benign granular cell tumor of gallbladder", "Benign Gallbladder Granular Cell Neoplasm", "benign granular cell tumor of gallbladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign granular cell tumor of gallbladder", "shortest_name_length": 38}
{"curie": "MONDO:0002872", "names": ["Trophoblast Tumor", "trophoblast tumor", "Tumor, Trophoblast", "Trophoblast Tumors", "Trophoblastic Tumor", "Trophoblastic tumor", "trophoblastic tumor", "Tumors, Trophoblast", "trophoblast neoplasm", "trophoblastic; tumor", "Tumor, Trophoblastic", "Trophoblastic tumour", "Trophoblastic Tumors", "tumor; trophoblastic", "Trophoblast Neoplasm", "tumor of trophoblast", "Trophoblastic tumors", "Neoplasm, Trophoblast", "Tumors, Trophoblastic", "Trophoblast Neoplasms", "trophoblastic neoplasm", "Trophoblastic Neoplasm", "Neoplasms, Trophoblast", "Trophoblastic neoplasm", "Trophoblastic Neoplasms", "Neoplasm, Trophoblastic", "TROPHOBLASTIC NEOPLASMS", "trophoblastic neoplasms", "Trophoblastic neoplasms", "neoplasm of trophoblast", "Neoplasms, Trophoblastic", "trophoblast neoplasm (disease)", "trophoblastic tumor (qualifier value)", "trophoblastic neoplasm (morphologic abnormality)", "Trophoblastic neoplasm (morphologic abnormality)", "trophoblastic neoplasm NOS (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trophoblastic neoplasm", "shortest_name_length": 17}
{"curie": "MONDO:0011358", "names": ["blue nevi, familial multiple", "Blue Nevi, Familial Multiple", "BLUE NEVI, FAMILIAL MULTIPLE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blue nevi, familial multiple", "shortest_name_length": 28}
{"curie": "MONDO:0010026", "names": ["syndrome short", "SHORT SYNDROME", "SHORT syndrome", "short syndrome", "Aarskog-Ose-Pande syndrome", "Rieger anomaly-partial lipodystrophy syndrome", "Lipodystrophy-Rieger anomaly-diabetes syndrome", "lipodystrophy-Rieger anomaly-diabetes syndrome", "partial lipodystrophy with Rieger anomaly and short stature", "LIPODYSTROPHY, PARTIAL, WITH RIEGER ANOMALY AND SHORT STATURE", "lipodystrophy, partial, with Rieger anomaly and short stature", "Lipodystrophy, Partial, With Rieger Anomaly, And Short Stature", "short stature, hyperextensibility, hernia, ocular depression, Rieger anomaly and teething delay", "SHORT STATURE, HYPEREXTENSIBILITY, HERNIA, OCULAR DEPRESSION, RIEGER ANOMALY, AND TEETHING DELAY", "short stature, hyperextensibility, hernia, ocular depression, Rieger anomaly, and teething delay"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SHORT syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0005127", "names": ["LL leprosy", "leprosy; LL", "LL; leprosy", "Type L leprosy", "type L leprosy", "Type LL leprosy", "Lepromatous Leprosy", "LEPROMATOUS LEPROSY", "lepromatous leprosy", "Lepromatous leprosy", "lepromatous; leprosy", "Leprosy, Lepromatous", "LEPROSY, LEPROMATOUS", "leprosy; lepromatous", "Lepromatous Leprosies", "Leprosies, Lepromatous", "Full lepromatous leprosy", "lepromatous leprosy [type L]", "Lepromatous leprosy [type L]", "LL - Full lepromatous leprosy", "HANSEN DISEASE, MALIGNANT FORM", "Lepromatous leprosy (disorder)", "lepromatous leprosy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lepromatous leprosy", "shortest_name_length": 10}
{"curie": "UMLS:C0280382", "names": ["nasopharynx squamous cell carcinoma, stage III", "Nasopharyngeal squamous cell carcinoma stage III", "nasopharyngeal squamous cell carcinoma, stage III", "epidermoid carcinoma of the nasopharynx, stage III", "stage III squamous cell carcinoma of the nasopharynx", "squamous cell carcinoma of the nasopharynx, stage III", "Stage III Nasopharyngeal Keratinizing Epidermoid Carcinoma", "Stage III Keratinizing Epidermoid Carcinoma of Nasopharynx", "Stage III Keratinizing Squamous Cell Carcinoma of Nasopharynx", "Stage III Nasopharyngeal Keratinizing Squamous Cell Carcinoma", "Stage III Keratinizing Epidermoid Carcinoma of the Nasopharynx", "Stage III Keratinizing Squamous Cell Carcinoma of the Nasopharynx", "Stage III Nasopharyngeal Throat Keratinizing Squamous Cell Cancer", "Stage III Nasopharyngeal Keratinizing Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasopharyngeal squamous cell carcinoma stage III", "shortest_name_length": 46}
{"curie": "MONDO:0012493", "names": ["RLS4", "RLS 4", "restless legs syndrome 4", "RESTLESS LEGS SYNDROME, SUSCEPTIBILITY TO, 4", "restless legs syndrome, susceptibility to, 4", "RESTLESS LEGS SYNDROME, SUSCEPTIBILITY TO, 4 (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "restless legs syndrome, susceptibility to, 4", "shortest_name_length": 4}
{"curie": "UMLS:C0948820", "names": ["Catheter site rash"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Catheter site rash", "shortest_name_length": 18}
{"curie": "MONDO:0016125", "names": ["infectious, fungal or parasitic myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infectious, fungal or parasitic myopathy", "shortest_name_length": 40}
{"curie": "UMLS:C4684839", "names": ["Perfusion Computed Tomography Target Lesion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perfusion Computed Tomography Target Lesion", "shortest_name_length": 43}
{"curie": "MONDO:0012030", "names": ["DFNA43", "autosomal dominant deafness 43", "Deafness, Autosomal Dominant 43", "DEAFNESS, AUTOSOMAL DOMINANT 43", "deafness, autosomal dominant 43", "DEAFNESS, AUTOSOMAL DOMINANT 43 (disorder)", "autosomal dominant nonsyndromic deafness 43", "autosomal dominant nonsyndromic hearing loss 43", "autosomal dominant nonsyndromic deafness type 43"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 43", "shortest_name_length": 6}
{"curie": "UMLS:C0857353", "names": ["Hypotensive", "hypotensive", "hypotensives"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypotensive", "shortest_name_length": 11}
{"curie": "UMLS:C1300202", "names": ["Diaphyseal medullary stenosis with bone malignancy", "diaphyseal medullary stenosis with bone malignancy", "Diaphyseal medullary stenosis with bone malignancy (disorder)", "diaphyseal medullary stenosis with bone malignancy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diaphyseal medullary stenosis with bone malignancy", "shortest_name_length": 50}
{"curie": "MONDO:0013949", "names": ["CGH", "CG13", "PBD11A", "peroxisome biogenesis disorder 11A", "peroxisome biogenesis disorder 11A (Zellweger)", "PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER)", "Peroxisome Biogenesis Disorder, Complementation Group H", "PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP H", "peroxisome biogenesis disorder, complementation group H", "PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 13", "peroxisome biogenesis disorder, complementation group 13", "Peroxisome Biogenesis Disorder, Complementation Group 13"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder 11A (Zellweger)", "shortest_name_length": 3}
{"curie": "MONDO:0003922", "names": ["Clear cell adenocarcinofibroma", "Ovarian Clear Cell Adenocarcinofibroma", "ovarian clear cell adenocarcinofibroma", "clear cell adenocarcinofibroma of ovary", "Ovarian Clear Cell Malignant Adenofibroma", "ovarian clear cell malignant adenofibroma", "clear cell adenocarcinofibroma of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian clear cell malignant adenofibroma", "shortest_name_length": 30}
{"curie": "MONDO:0100094", "names": ["CHS", "cannabinoid hyperemesis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cannabinoid hyperemesis syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C1334183", "names": ["Central Nervous System Inflammatory Myofibroblastic Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Inflammatory Myofibroblastic Tumor", "shortest_name_length": 57}
{"curie": "UMLS:C1333384", "names": ["Endemic African Kaposi Sarcoma", "Endemic African Kaposi's Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endemic African Kaposi Sarcoma", "shortest_name_length": 30}
{"curie": "UMLS:C2983719", "names": ["Nasopharyngeal Carcinoma by AJCC v6 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasopharyngeal Carcinoma by AJCC v6 Stage", "shortest_name_length": 41}
{"curie": "MONDO:0010655", "names": ["MRXSLF", "Lujan Syndrome", "Lujan syndrome", "Lujan Fryns syndrome", "LUJAN-Fryns syndrome", "Lujan-Fryns Syndrome", "Lujan-Fryns syndrome", "LUJAN-FRYNS SYNDROME", "XLMR with Marfanoid Features", "Lujan-Fryns syndrome, X-linked recessive", "X-Linked Mental Retardation with Marfanoid Habitus", "X-Linked Intellectual Deficit with Marfanoid Habitus", "Mental retardation, X-linked, with marfanoid habitus", "mental retardation, X-linked, with Marfanoid habitus", "X-linked mental retardation-marfanoid habitus syndrome", "X-linked intellectual disability with marfanoid habitus", "MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS, 1", "intellectual disability, X-linked, with Marfanoid habitus", "syndromic X-linked intellectual disorder Lujan-Fryns-type", "X-linked mental retardation with marfanoid habitus syndrome", "X-linked intellectual disability with Marfanoid habitus syndrome", "X-linked intellectual disability with marfanoid habitus (disorder)", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUJAN-FRYNS TYPE", "X-linked intellectual disability with Marfanoid habitus syndrome (diagnosis)", "Marfanoid habitus, mild general hypotonia, hypernasal voice, normal testicular size and distinct craniofacial anomalies", "Marfanoid habitus, mild general hypotonia, hypernasal voice, normal testicular size, and distinct craniofacial anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability with marfanoid habitus", "shortest_name_length": 6}
{"curie": "UMLS:C0001510", "names": ["Postoperative adhesion", "Adhesion, postoperative", "Adhesions NOS postoperative", "Postoperative adhesion (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postoperative adhesion", "shortest_name_length": 22}
{"curie": "UMLS:C5238965", "names": ["Steroid Resistant Acute Graft Versus Host Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Steroid Resistant Acute Graft Versus Host Disease", "shortest_name_length": 49}
{"curie": "MONDO:0005696", "names": ["brain tuberculoma", "tuberculoma of brain", "Tuberculoma of brain", "brain of tuberculoma", "Intracranial Tuberculoma", "intracranial tuberculoma", "Tuberculoma, Intracranial", "tuberculous brain abscess", "tuberculous abscess of brain", "Tuberculous abscess of brain", "Tuberculoma of brain (disorder)", "Tuberculous intracranial abscess", "Tuberculoma of brain, unspecified", "central nervous system tuberculosis", "intracranial tuberculoma (diagnosis)", "tuberculous brain abscess (diagnosis)", "Tuberculous abscess of brain (disorder)", "Tuberculous intracranial abscess (disorder)", "brain abscess due to Mycobacterium tuberculosis", "tuberculosis of meninges and central nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system tuberculosis", "shortest_name_length": 17}
{"curie": "UMLS:C4525116", "names": ["Stage 0 Colon Cancer", "Stage 0 Colon Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Colon Cancer AJCC v8", "shortest_name_length": 20}
{"curie": "MONDO:0009294", "names": ["Hers", "GSD6", "GSD 6", "GSD VI", "GSD type 6", "Her Disease", "GSD type VI", "hers disease", "Hers Disease", "HERS DISEASE", "Hers disease", "Disease, Hers", "her's disease", "Hers' disease", "Hers' Disease", "hers' disease", "Her's disease", "Glycogenosis 6", "Disease, Hers'", "Glycogenosis VI", "Hers glycogenosis", "glycogenosis type 6", "Glycogenosis type 6", "Glycogenosis Type VI", "Glycogenosis type VI", "glycogenosis type VI", "GLYCOGENOSIS, TYPE VI", "Type VI, Glycogenosis", "Hers disease (GSD type VI)", "glycogen storage disease 6", "Glycogen storage disease 6", "glycogen storage disease VI", "GLYCOGEN STORAGE DISEASE VI", "PYGL glycogen storage disease", "Liver phosphorylase deficiency", "liver phosphorylase deficiency", "LIVER PHOSPHORYLASE DEFICIENCY", "hepatophosphorylase; deficiency", "glycogen storage disease type 6", "deficiency; hepatophosphorylase", "liver phosphorylase; deficiency", "deficiency; liver phosphorylase", "Glycogen storage disease type 6", "Glycogen storage disease type VI", "GLYCOGEN STORAGE DISEASE TYPE VI", "Glycogen Storage Disease Type VI", "glycogen storage disease type VI", "Hepatic phosphorylase deficiency", "hepatic phosphorylase deficiency", "Glycogen storage disease, type VI", "Hers disease (GSD type VI) (diagnosis)", "Liver glycogen phosphorylase deficiency", "Liver phosphorylase deficiency syndrome", "Liver Phosphorylase Deficiency Syndrome", "liver glycogen phosphorylase deficiency", "hepatic glycogen phosphorylase deficiency", "Hepatic Glycogen Phosphorylase Deficiency", "Hepatic glycogen phosphorylase deficiency", "HEPATOPHOSPORYLASE DEFICIENCY GLYCOGENOSIS", "hepatophosphorylase deficiency glycogenosis", "Glycogen storage disease, type VI (disorder)", "GSD due to liver glycogen phosphorylase deficiency", "glycogen storage disease caused by mutation in PYGL", "PHOSPHORYLASE DEFICIENCY GLYCOGEN-STORAGE DISEASE OF LIVER", "phosphorylase deficiency glycogen-storage disease of liver", "Glycogenosis due to liver glycogen phosphorylase deficiency", "glycogenosis due to liver glycogen phosphorylase deficiency", "glycogen storage disease due to liver glycogen phosphorylase deficiency", "Glycogen storage disease due to liver glycogen phosphorylase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease VI", "shortest_name_length": 4}
{"curie": "UMLS:C0263369", "names": ["Retiform parapsoriasis", "Retiform Parapsoriasis", "parapsoriasis retiform", "retiform parapsoriasis", "Parapsoriasis Variegata", "Parapsoriasis variegata", "parapsoriasis; retiform", "retiform; parapsoriasis", "Parapsoriasis lichenoides", "Parapsoriasis Lichenoides", "Poikilodermic Parapsoriasis", "Poikilodermic parapsoriasis", "Retiform parapsoriasis (disorder)", "Poikiloderma Atrophicans Vasculare", "retiform parapsoriasis (diagnosis)", "Poikiloderma vasculare atrophicans", "poikiloderma vasculare atrophicans", "Poikiloderma atrophicans vasculare", "poikiloderma; vasculare atrophicans", "vasculare atrophicans; poikiloderma", "Parapsoriasis lichenoides (disorder)", "poikiloderma vasculare atrophicans (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parapsoriasis lichenoides", "shortest_name_length": 22}
{"curie": "UMLS:C1336536", "names": ["Supratentorial Glioblastoma", "Supratentorial Glioblastoma Multiforme"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Supratentorial Glioblastoma", "shortest_name_length": 27}
{"curie": "MONDO:0006060", "names": ["Nasopharyngeal squamous cell carcinoma", "nasopharyngeal squamous cell carcinoma", "Squamous cell carcinoma of nasopharynx", "squamous cell carcinoma of nasopharynx", "Nasopharyngeal Squamous Cell Carcinoma", "Squamous cell carcinoma of nasopharynx (disorder)", "squamous cell carcinoma of nasopharynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasopharyngeal squamous cell carcinoma", "shortest_name_length": 38}
{"curie": "MONDO:0016316", "names": ["MPS2B", "MPSIIB", "Hunter syndrome type B", "mucopolysaccharidosis type 2B", "mucopolysaccharidosis type IIB", "iduronate 2-sulfatase deficiency type B", "mucopolysaccharidosis type 2, attenuated form", "mucopolysaccharidosis type II, attenuated form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucopolysaccharidosis type 2, attenuated form", "shortest_name_length": 5}
{"curie": "MONDO:0043768", "names": ["Thrombopenic Purpura", "thrombopenic purpura", "Thrombopenic purpura", "Purpura, Thrombopenic", "Thrombopenic Purpuras", "purpura, thrombopenic", "thrombopenic purpuras", "thrombopenic; purpura", "purpura; thrombopenic", "Purpuras, Thrombopenic", "purpuras, thrombopenic", "THROMBOCYTOPENIA PURPURA", "Thrombocytopenia purpura", "THROMBOCYTOPENIC PURPURA", "Thrombocytopenic Purpura", "Purpura thrombocytopenic", "thrombocytopenic purpura", "Thrombocytopenic purpura", "PURPURA THROMBOCYTOPENIC", "Thrombocytopaenic purpura", "Purpura, Thrombocytopenic", "thrombocytopenic purpuras", "thrombocytopaenic purpura", "purpura thrombocytopaenic", "purpura; thrombocytopenic", "Thrombocytopenic Purpuras", "thrombocytopenic; purpura", "purpuras, thrombocytopenic", "Purpuras, Thrombocytopenic", "Thrombocytopenic purpura (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombocytopenic purpura", "shortest_name_length": 20}
{"curie": "UMLS:C0302507", "names": ["Parainfluenza Infection", "Parainfluenza Virus Infection", "Parainfluenzae virus infection", "Virus Infection, Parainfluenza", "Parainfluenza Virus Infections", "Infection, Parainfluenza Virus", "Virus Infections, Parainfluenza", "Infections, Parainfluenza Virus", "Parainfluenzae virus infection NOS", "viral; infection, parainfluenza virus", "infection; viral, parainfluenza virus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parainfluenza Virus Infections", "shortest_name_length": 23}
{"curie": "MONDO:0019963", "names": ["bronchus NET", "bronchial NET", "bronchial endocrine tumor", "bronchus neuroendocrine tumor", "bronchial neuroendocrine tumor", "bronchus neuroendocrine neoplasm", "neuroendocrine neoplasm of bronchus", "bronchus neuroendocrine tumor, well differentiated, low or intermediate grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bronchial endocrine tumor", "shortest_name_length": 12}
{"curie": "UMLS:C1336015", "names": ["Smoldering Adult T-Cell Lymphoma/Leukemia", "Smoldering Adult T-Cell Leukemia/Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Smoldering Adult T-Cell Leukemia/Lymphoma", "shortest_name_length": 41}
{"curie": "UMLS:C1879280", "names": ["angiocentric T-cell lymphoma", "Nasal Type Extranodal NK/T-Cell Lymphoma", "Childhood Nasal Type Extranodal NK/T-Cell Lymphoma", "childhood nasal type extranodal NK/T-cell lymphoma", "childhood nasal type extranodal natural killer/T-cell lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood nasal type extranodal NK/T-cell lymphoma", "shortest_name_length": 28}
{"curie": "MONDO:0015032", "names": ["Intraneural perineurioma", "Intraneural Perineurioma", "intraneural perineurioma", "Intraneural perineurioma (disorder)", "intraneural perineurioma (WHO grade I)", "Intraneural Perineurioma (WHO Grade I)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intraneural perineurioma", "shortest_name_length": 24}
{"curie": "UMLS:C0854212", "names": ["Subepithelial opacities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subepithelial opacities", "shortest_name_length": 23}
{"curie": "UMLS:C4725952", "names": ["Locally Advanced Gastrointestinal Stromal Tumor", "Locally Advanced Gastrointestinal Stromal Tumor (GIST)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Gastrointestinal Stromal Tumor", "shortest_name_length": 47}
{"curie": "MONDO:0017524", "names": ["preaxial polydactyly type 1, bilateral", "polydactyly of a biphalangeal thumb, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polydactyly of a biphalangeal thumb, bilateral", "shortest_name_length": 38}
{"curie": "UMLS:C0854993", "names": ["Stage III Squamous Cell Lung Cancer", "Lung squamous cell carcinoma stage III", "Stage III Squamous Cell Lung Carcinoma", "Lung Squamous Cell Carcinoma Stage III", "Stage III Epidermoid Cell Lung Carcinoma", "Stage III Squamous Cell Carcinoma of Lung", "Squamous cell carcinoma of lung stage III", "Stage III Epidermoid Cell Carcinoma of Lung", "Stage III Squamous Cell Carcinoma of the Lung", "Stage III Lung Squamous Cell Carcinoma AJCC v7", "Stage III Squamous Cell Lung Carcinoma AJCC v7", "Stage III Epidermoid Cell Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung squamous cell carcinoma stage III", "shortest_name_length": 35}
{"curie": "MONDO:0024281", "names": ["Juvenile Chronic Polyarthritis", "juvenile chronic polyarthritis", "Juvenile chronic polyarthritis", "Polyarticular juvenile arthritis", "Juvenile chronic polyarthritis, NOS", "Polyarticular onset juvenile chronic arthritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile chronic polyarthritis", "shortest_name_length": 30}
{"curie": "MONDO:0014689", "names": ["KFS4", "Klippel-Feil syndrome 4", "Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome", "Klippel-Feil anomaly, myopathy, facial dysmorphism syndrome", "Klippel-Feil anomaly, myopathy, facial dysmorphism syndrome (disorder)", "Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism", "Klippel-Feil syndrome 4, autosomal recessive, with nemaline myopathy and facial dysmorphism", "KLIPPEL-FEIL SYNDROME 4, AUTOSOMAL RECESSIVE, WITH NEMALINE MYOPATHY AND FACIAL DYSMORPHISM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0045038", "names": ["cutaneous basidiobolomycosis", "Cutaneous basidiobolomycosis", "Cutaneous basidiobolomycosis (disorder)", "Cutaneous basidiobolomycosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous basidiobolomycosis", "shortest_name_length": 28}
{"curie": "UMLS:C5236960", "names": ["Unresectable Head and Neck Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Head and Neck Carcinoma", "shortest_name_length": 36}
{"curie": "MONDO:0032624", "names": ["MC1DN19", "nuclear type mitochondrial complex I deficiency 19", "mitochondrial complex 1 deficiency, nuclear type 19", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 19"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 19", "shortest_name_length": 7}
{"curie": "UMLS:C0854838", "names": ["Angiocentric lymphoma stage IV", "Stage IV Angiocentric Lymphoma", "Nasal T-cell lymphoma stage IV", "Angiocentric Lymphoma Stage IV", "Polymorphic reticulosis stage IV", "Stage IV Nasal Type NK/T-Cell Lymphoma", "Ann Arbor Stage IV Nasal Type NK/T-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Angiocentric lymphoma stage IV", "shortest_name_length": 30}
{"curie": "MONDO:0006810", "names": ["Pseudotumor cerebri", "CSF pressure increased", "Intracranial hypertension", "intracranial hypertension", "hypertension intracranial", "INTRACRANIAL HYPERTENSION", "Hypertension intracranial", "Intracranial Hypertension", "HYPERTENSION INTRACRANIAL", "Hypertension, Intracranial", "hypertension; intracranial", "hypertensions intracranial", "intracranial; hypertension", "raised intracranial pressure", "intracranial pressure raised", "Raised intracranial pressure", "Rise in pressure inside skull", "Intracranial hypertension NOS", "Elevated Intracranial Pressure", "Elevated intracranial pressure", "intracranial pressure increase", "Intracranial Pressure Increase", "Intracranial pressure increase", "increase intracranial pressure", "Pressure Increase, Intracranial", "Intracranial Pressure, Elevated", "INTRACRANIAL PRESSURE INCREASED", "Increased Intracranial Pressure", "increased intracranial pressure", "Pressure, Elevated Intracranial", "intracranial increased pressure", "PRESSURE INTRACRANIAL INCREASED", "Pressure intracranial increased", "Intracranial pressure increased", "Increased intracranial pressure", "Intracranial pressure elevation", "INTRACRANIAL PRESSURE, INCREASED", "increased; intracranial pressure", "intracranial pressure; increased", "RIP - Raised intracranial pressure", "Intracranial pressure increased NOS", "ICP (Intracranial Pressure) Increase", "Elevated ICP (Intracranial Pressure)", "ICP (Intracranial Pressure) Elevation", "ICP, Elevated (Intracranial Pressure)", "Raised intracranial pressure (finding)", "Pressure cerebrospinal fluid increased", "Increased cerebrospinal fluid pressure", "Cerebrospinal fluid pressure increased", "PRESSURE CEREBROSPINAL FLUID INCREASED", "Cerebrospinal fluid pressure, increased", "Increase in intracranial pressure (ICP)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intracranial hypertension", "shortest_name_length": 19}
{"curie": "UMLS:C0399439", "names": ["Drug Induced Gingival Hyperplasia", "Drug-induced gingival hyperplasia", "Gingival enlargement - drug-induced", "Hyperplasia of gingiva caused by drug", "Hyperplasia of gingiva caused by drug (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drug-induced gingival hyperplasia", "shortest_name_length": 33}
{"curie": "UMLS:C5447596", "names": ["Refractory Male Reproductive System Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Male Reproductive System Carcinoma", "shortest_name_length": 45}
{"curie": "MONDO:0019636", "names": ["Single kidney", "Single Kidney", "Single Kidneys", "Kidney, Single", "Solitary Kidney", "Kidneys, Single", "SOLITARY KIDNEY", "Solitary kidney", "solitary kidney", "kidneys solitary", "Missing one kidney", "congenital single kidney", "Congenital Single Kidney", "Unilateral renal agenesis", "Unilateral Renal Agenesis", "renal agenesis unilateral", "renal unilateral agenesis", "Absent kidney on one side", "unilateral renal agenesis", "Single Functioning Kidney", "Congenital Solitary Kidney", "Kidney, Single Functioning", "Unilateral kidney agenesis", "Renal Agenesis, Unilateral", "Renal agenesis, unilateral", "Single Functioning Kidneys", "Functioning Kidney, Single", "congenital solitary kidney", "renal agenesis, unilateral", "Solitary Functioning Kidney", "Functioning Kidneys, Single", "Kidneys, Single Functioning", "Kidney agenesis, unilateral", "solitary; kidney, congenital", "kidney; agenesis, unilateral", "kidney; solitary, congenital", "congenital absence of kidney", "Unilateral agenesis of kidney", "agenesis; kidney(s), unilateral", "Congenital absence of one kidney", "congenital absence of one kidney", "absence of one kidney congenital", "Unilateral congenital absence of kidney", "kidney; absence, congenital, unilateral", "congenital absence of one kidney (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal agenesis, unilateral", "shortest_name_length": 13}
{"curie": "UMLS:C1706987", "names": ["Borrelia Burgdoferi-Associated Cutaneous Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue", "Borrelia Burgdoferi-Associated Cutaneous Marginal Zone B-Cell Lymphoma of Mucosa-Associated Lymphoid Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borrelia Burgdoferi-Associated Cutaneous Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue", "shortest_name_length": 100}
{"curie": "MONDO:0013212", "names": ["CMT2N", "Charcot-Marie-Tooth disease type 2N", "AARS Charcot-Marie-Tooth disease type 2", "Charcot-Marie-Tooth disease axonal type 2N", "Charcot-Marie-Tooth Disease, Axonal, Type 2n", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2N", "Charcot-Marie-Tooth disease, axonal, type 2N", "Charcot-Marie-Tooth neuropathy axonal type 2N", "Charcot-Marie-Tooth Neuropathy, Axonal, Type 2n", "CHARCOT-MARIE-TOOTH NEUROPATHY, AXONAL, TYPE 2N", "Charcot-Marie-Tooth neuropathy, axonal, type 2N", "autosomal dominant Charcot-Marie-Tooth disease type 2N", "Autosomal dominant Charcot-Marie-Tooth disease type 2N", "autosomal dominant axonal Charcot-Marie-Tooth disease type 2N", "Charcot-Marie-Tooth disease type 2 caused by mutation in AARS", "Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2n", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2N", "Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2N", "Autosomal dominant Charcot-Marie-Tooth disease type 2N (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease axonal type 2N", "shortest_name_length": 5}
{"curie": "UMLS:C0521595", "names": ["Duodenal bleeding", "Duodenal Hemorrhage", "duodenal hemorrhage", "Hemorrhage duodenum", "Duodenal hemorrhage", "HEMORRHAGE DUODENUM", "hemorrhage; duodenum", "Duodenal haemorrhage", "duodenum; hemorrhage", "Haemorrhage duodenum", "Duodenal hemorrhage, NOS", "Duodenal haemorrhage, NOS", "Duodenal hemorrhage (disorder)", "duodenal hemorrhage (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Duodenal hemorrhage", "shortest_name_length": 17}
{"curie": "UMLS:C1332189", "names": ["Adult Brain Meningioma", "Adult Intracranial Meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Intracranial Meningioma", "shortest_name_length": 22}
{"curie": "UMLS:C1336202", "names": ["Stage IIC", "Stage IIC Cancer of Testis", "stage IIC cancer of testis", "Stage IIC Testicular Cancer", "stage IIC testicular cancer", "Stage IIC Cancer of the Testis", "stage IIC cancer of the testis", "Stage IIC Testicular Cancer AJCC v7", "stage IIC testicular cancer AJCC v7", "Stage IIC Testicular Cancer AJCC v6", "stage IIC testicular cancer AJCC v6", "Stage IIC Testicular Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIC Testicular Cancer AJCC v6 and v7", "shortest_name_length": 9}
{"curie": "MONDO:0009587", "names": ["MEXICAN CARDIOMELIC DYSPLASIA", "Mexican Cardiomelic Dysplasia", "Mexican cardiomelic dysplasia", "Mexican Cardiomelic dysplasia", "MESOAXIAL HEXADACTYLY AND CARDIAC MALFORMATION", "Mesoaxial Hexadactyly and Cardiac Malformation", "mesoaxial hexadactyly and cardiac malformation", "mesoaxial hexadactyly-cardiac malformation syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mesoaxial hexadactyly and cardiac malformation", "shortest_name_length": 29}
{"curie": "UMLS:C2828014", "names": ["Stage IIB Merkel Cell Carcinoma", "Stage IIB Merkel Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Merkel Cell Carcinoma AJCC v7", "shortest_name_length": 31}
{"curie": "MONDO:0009759", "names": ["MVA1", "MVA syndrome", "mosaic variegated aneuploidy syndrome 1", "MOSAIC variegated aneuploidy syndrome 1", "BUB1B mosaic variegated aneuploidy syndrome", "Mosaic variegated aneuploidy syndrome type 1", "mosaic variegated aneuploidy syndrome type 1", "mosaic variegated aneuploidy syndrome caused by mutation in BUB1B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mosaic variegated aneuploidy syndrome 1", "shortest_name_length": 4}
{"curie": "UMLS:C3898352", "names": ["Mild BPD", "Mild Bronchopulmonary Dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mild Bronchopulmonary Dysplasia", "shortest_name_length": 8}
{"curie": "MONDO:0015140", "names": ["EOFAD", "early-onset autosomal dominant Alzheimer disease", "early-onset, autosomal dominant Alzheimer disease", "early-onset familial autosomal dominant Alzheimer disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early-onset autosomal dominant Alzheimer disease", "shortest_name_length": 5}
{"curie": "MONDO:0006058", "names": ["Wilms tumor", "Wilms Tumor", "Wilms' tumor", "Wilms' Tumor", "Nephroblastoma", "Wilms tumor (WT)", "Wilms tumor (nephroblastoma)", "Wilms tumor (Nephroblastoma)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wilms tumor", "shortest_name_length": 11}
{"curie": "MONDO:0008389", "names": ["autosomal dominant Robinow syndrome", "Robinow syndrome, autosomal dominant", "Robinow syndrome, autosomal dominant type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant Robinow syndrome", "shortest_name_length": 35}
{"curie": "MONDO:0019851", "names": ["acquired primary ovarian failure", "Acquired premature ovarian failure", "acquired premature ovarian failure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired primary ovarian failure", "shortest_name_length": 32}
{"curie": "MONDO:0016687", "names": ["Protoplasmic Astrocytoma", "Protoplasmic astrocytoma", "protoplasmic astrocytoma", "Protoplasmic Astrocytomas", "Astrocytoma, Protoplasmic", "Protoplasmic Astrocytic tumor", "protoplasmic astrocytic tumor", "Protoplasmic astrocytoma (morphologic abnormality)", "protoplasmic astrocytoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "protoplasmic astrocytoma", "shortest_name_length": 24}
{"curie": "MONDO:0001506", "names": ["Prostatocystitis", "prostatocystitis", "prostatitis; cystitis", "cystitis; prostatitis", "Prostatocystitis (disorder)", "prostatocystitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostatocystitis", "shortest_name_length": 16}
{"curie": "MONDO:0036976", "names": ["benign epithelioma", "Benign epithelioma", "Benign Epithelioma", "EPITHELIOMA, BENIGN", "epithelioma, benign", "Epithelioma, benign", "Benign epithelial tumor", "benign epithelial tumor", "Benign Epithelial Tumor", "Benign epithelial tumour", "Epithelial tumor, benign", "Epithelial tumour, benign", "benign tumor of epithelium", "Benign epithelial neoplasm", "Benign Tumor of Epithelium", "Benign Epithelial Neoplasm", "benign epithelial neoplasm", "epithelial neoplasm, benign", "Benign Neoplasm of Epithelium", "benign neoplasm of epithelium", "Benign Tumor of the Epithelium", "benign tumor of the epithelium", "benign neoplasm of the epithelium", "Benign Neoplasm of the Epithelium", "Epithelioma, benign (morphologic abnormality)", "Benign epithelial neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign epithelial neoplasm", "shortest_name_length": 18}
{"curie": "UMLS:C0334364", "names": ["Papillary Mucinous Cystadenocarcinoma", "Papillary mucinous cystadenocarcinoma", "Papillary pseudomucinous adenocarcinoma", "Papillary pseudomucinous cystadenocarcinoma", "cystadenocarcinoma; mucinous, papillary, unspecified site", "papillary; cystadenocarcinoma, mucinous, unspecified site", "mucinous; cystadenocarcinoma, papillary, unspecified site", "cystadenocarcinoma; papillary, mucinous, unspecified site", "Papillary mucinous cystadenocarcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Papillary mucinous cystadenocarcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0014429", "names": ["IMD27B", "immunodeficiency 27B", "IMMUNODEFICIENCY 27B", "immunodeficiency type 27B", "autosomal dominant IFNGR1 deficiency", "IFNGR1 DEFICIENCY, AUTOSOMAL DOMINANT", "IFNGR1 deficiency, autosomal dominant", "immunodeficiency 27B, mycobacteriosis, AD", "autosomal dominant immunodeficiency 27B, mycobacteriosis", "immunodeficiency 27B, Mycobacteriosis, autosomal dominant", "IMMUNODEFICIENCY 27B, MYCOBACTERIOSIS, AUTOSOMAL DOMINANT", "autosomal dominant MSMD due to partial IFNgammaR1 deficiency", "autosomal dominant MSMD due to partial interferon gamma receptor 1 deficiency", "IFNGR1 autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency", "autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency", "autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 1 deficiency", "autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency caused by mutation in IFNGR1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency", "shortest_name_length": 6}
{"curie": "MONDO:0020574", "names": ["nongerminomatous GCT - CNS", "Nongerminomatous GCT - CNS", "nongerminomatous germ cell tumor of the CNS", "Nongerminomatous germ cell tumor of the CNS", "Nongerminomatous germ cell tumour of the CNS", "central nervous system nongerminomatous germ cell tumor", "Central Nervous System Nongerminomatous Germ Cell Tumor", "Nongerminomatous germ cell tumor of central nervous system", "Nongerminomatous germ cell tumour of central nervous system", "Nongerminomatous germ cell tumor of the central nervous system", "Nongerminomatous germ cell tumor of central nervous system (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system nongerminomatous germ cell tumor", "shortest_name_length": 26}
{"curie": "UMLS:C5446445", "names": ["Lacrimal Drainage System Non-Keratinizing Squamous Cell Carcinoma", "Non-Keratinizing Squamous Cell Carcinoma of the Lacrimal Drainage System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lacrimal Drainage System Non-Keratinizing Squamous Cell Carcinoma", "shortest_name_length": 65}
{"curie": "UMLS:C0686114", "names": ["malignant neoplasm extrahepatic bile duct secondary", "Secondary malignant neoplasm of extrahepatic bile ducts", "Metastatic malignant neoplasm to extrahepatic bile ducts", "Metastatic malignant neoplasm of extrahepatic bile ducts", "Secondary malignant neoplasm of extrahepatic bile ducts, NOS", "Metastatic Malignant Neoplasm to the Extrahepatic Bile Ducts", "Metastatic Malignant Neoplasm in the Extrahepatic Bile Ducts", "Metastatic malignant neoplasm to extrahepatic bile ducts, NOS", "Metastatic malignant neoplasm to extrahepatic bile ducts (disorder)", "Secondary malignant neoplasm of extrahepatic bile ducts (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to extrahepatic bile ducts", "shortest_name_length": 51}
{"curie": "UMLS:C2010420", "names": ["Cerebral Ganglioneuroblastoma", "Central Nervous System Ganglioneuroblastoma", "ganglioneuroblastoma of central nervous system", "Ganglioneuroblastoma of central nervous system", "Ganglioneuroblastoma of CNS (central nervous system)", "Ganglioneuroblastoma of central nervous system (disorder)", "ganglioneuroblastoma of central nervous system (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Ganglioneuroblastoma", "shortest_name_length": 29}
{"curie": "MONDO:0005437", "names": ["testicular dysgenesis syndrome", "Testicular dysgenesis syndrome", "Testicular dysgenesis syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular dysgenesis syndrome", "shortest_name_length": 30}
{"curie": "MONDO:0000093", "names": ["Schistosoma mansoni infection, susceptibility"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Schistosoma mansoni infection, susceptibility", "shortest_name_length": 45}
{"curie": "MONDO:0000678", "names": ["simultanagnosia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "simultanagnosia", "shortest_name_length": 15}
{"curie": "UMLS:C0877064", "names": ["Cerebral ventricle dilatation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebral ventricle dilatation", "shortest_name_length": 29}
{"curie": "MONDO:0015690", "names": ["Myeloid neoplasm with PDGFRB rearrangement", "Myeloid Neoplasms with PDGFRB Rearrangement", "myeloid neoplasms with PDGFRB rearrangement", "Myeloid neoplasms with PDGFRB rearrangement", "myeloid/lymphoid neoplasms with PDGFRB rearrangement", "Myeloid/Lymphoid Neoplasms with PDGFRB Rearrangement", "myeloid neoplasm associated with PDGFRB rearrangement", "Myeloid neoplasm associated with PDGFRB rearrangement", "myeloid neoplasms associated with PDGFRB rearrangement", "myeloid and lymphoid neoplasms with PDGFRB rearrangement", "Myeloid and Lymphoid Neoplasms with PDGFRB Rearrangement", "myeloid/lymphoid neoplasm associated with PDGFRB rearrangement", "myeloid neoplasm associated with PDGFRB rearrangement (diagnosis)", "myeloid and lymphoid neoplasms associated with PDGFRB rearrangement", "Myeloid neoplasm with beta-type platelet-derived growth factor receptor gene rearrangement", "Myeloid neoplasm associated with beta-type platelet-derived growth factor receptor gene rearrangement", "Myeloid neoplasm associated with beta-type platelet-derived growth factor receptor gene rearrangement (disorder)", "Myeloid neoplasm with beta-type platelet-derived growth factor receptor gene rearrangement (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myeloid neoplasm associated with PDGFRB rearrangement", "shortest_name_length": 42}
{"curie": "UMLS:C4521000", "names": ["Stage I Colon Cancer", "Colon Cancer Stage I", "Colon Cancer, Stage I", "Stage I Colon Carcinoma", "Dukes A Colon Carcinoma", "Stage I Colonic Carcinoma", "AJCC Stage I Colon Cancer", "Dukes A Colonic Carcinoma", "Dukes A Carcinoma of Colon", "Stage I Carcinoma of Colon", "Stage I Colon Cancer AJCC v7", "Stage I Colon Cancer AJCC v6", "Dukes A Carcinoma of the Colon", "Stage I Carcinoma of the Colon", "Stage I Colon Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Colon Cancer AJCC v6 and v7", "shortest_name_length": 20}
{"curie": "MONDO:0007617", "names": ["CSS", "CSS1", "MRD12", "fifth digit syndrome", "COFFIN-SIRIS syndrome", "COFFIN-SIRIS SYNDROME 1", "COFFIN-SIRIS syndrome 1", "Coffin-Siris syndrome 1", "ARID1B-related BAFopathy", "autosomal dominant mental retardation 12", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 12", "mental retardation, autosomal dominant 12", "intellectual disability, autosomal dominant 12", "mental retardation, autosomal dominant type 12", "hypertrichosis, hyperkeratosis, mental retardation, and distinctive facial features", "hypertrichosis, hyperkeratosis, intellectual disability, and distinctive facial features", "[OBSOLETE] Hypertrichosis, hyperkeratosis, mental retardation, and distinctive facial features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Coffin-Siris syndrome 1", "shortest_name_length": 3}
{"curie": "UMLS:C4275160", "names": ["Infection of skin of eyelid and periocular region", "infection of skin of eyelid and periocular region", "Infection of skin of eyelid and periocular region (disorder)", "infection of skin of eyelid and periocular region (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infection of skin of eyelid and periocular region", "shortest_name_length": 49}
{"curie": "UMLS:C4518624", "names": ["chronic pulmonary aspergillosis", "Chronic pulmonary aspergillosis", "Chronic Pulmonary Aspergillosis", "Chronic pulmonary aspergillosis (disorder)", "chronic pulmonary aspergillosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic pulmonary aspergillosis", "shortest_name_length": 31}
{"curie": "MONDO:0006272", "names": ["Low-grade fibromyxoid sarcoma", "low grade fibromyxoid sarcoma", "Low grade fibromyxoid sarcoma", "low-grade fibromyxoid sarcoma", "Low Grade Fibromyxoid Sarcoma", "Low-grade fibromyxoid sarcoma (disorder)", "Low-grade fibromyxoid sarcoma (diagnosis)", "malignant neoplasm sarcoma low-grade fibromyxoid", "Low grade fibromyxoid sarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "low grade fibromyxoid sarcoma", "shortest_name_length": 29}
{"curie": "UMLS:C4683572", "names": ["Lugano Classification Stage III Adult Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage III Adult Lymphoma AJCC v8", "shortest_name_length": 54}
{"curie": "UMLS:C0398795", "names": ["immunodeficiency secondary", "secondary immunodeficiency", "Secondary immunodeficiency", "Secondary immune deficiency disorder", "secondary immune deficiency disorder", "Immune deficiency disorder, secondary", "Secondary immune deficiency disorder, NOS", "Secondary immune deficiency disorder (disorder)", "secondary immune deficiency disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary immune deficiency disorder", "shortest_name_length": 26}
{"curie": "MONDO:0002121", "names": ["Mononeuritis", "MONONEURITIS", "mononeuritis", "Mononeuritides", "Mononeuritis, NOS", "mononeuritis simplex", "Mononeuritis (disorder)", "mononeuritis (diagnosis)", "Mononeuritis of unspecified site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mononeuritis simplex", "shortest_name_length": 12}
{"curie": "UMLS:C1334553", "names": ["Major Salivary Gland Sarcoma", "Sarcoma of Major Salivary Gland", "Sarcoma of the Major Salivary Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Major Salivary Gland Sarcoma", "shortest_name_length": 28}
{"curie": "MONDO:0006582", "names": ["Blue nevus", "mongolian spot", "Mongolian spot", "Mongolian Spot", "Spot, Mongolian", "Mongolian spots", "mongolian spots", "Mongolian Macula", "Blue Sacral Spot", "Blue sacral spot", "blue sacral spot", "Mongolian macula", "Mongolian blue spot", "Mongolian Blue Spot", "mongolian blue spot", "blue mongolian spots", "Blue Spot, Mongolian", "Mongolian spot (disorder)", "Mongolian spots were observed", "Congenital dermal melanocytosis", "congenital dermal melanocytosis", "Mongolian spots (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mongolian spot", "shortest_name_length": 10}
{"curie": "MONDO:0003107", "names": ["Infratentorial Cancer", "infratentorial cancer", "Infratentorial Cancers", "Cancer, Infratentorial", "Infratentorial Neoplasms", "Malignant Infratentorial Tumor", "brain neoplasm, infratentorial", "brain neoplasm, Infratentorial", "malignant infratentorial tumor", "malignant infratentorial tumors", "Malignant Infratentorial Tumors", "malignant Infratentorial tumors", "malignant infratentorial neoplasm", "Malignant Infratentorial Neoplasm", "Malignant Infratentorial Neoplasms", "Neoplasm, Malignant Infratentorial", "Infratentorial Neoplasm, Malignant", "Neoplasms, Malignant Infratentorial", "infratentorial neoplasms, malignant", "Infratentorial Neoplasms, Malignant", "Infratentorial malignant neoplasm NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infratentorial cancer", "shortest_name_length": 21}
{"curie": "MONDO:0001613", "names": ["Vertebrobasilar Ischemia", "vertebrobasilar ischemia", "Vertebrobasilar Ischemias", "Vertebro-Basilar Ischemia", "Vertebro Basilar Ischemia", "Ischemia, Vertebrobasilar", "Vertebro-Basilar Ischemias", "Ischemias, Vertebrobasilar", "Ischemia, Vertebro-Basilar", "Ischemias, Vertebro-Basilar", "vertebrobasilar insufficiency", "VERTEBROBASILAR INSUFFICIENCY", "Vertebrobasilar insufficiency", "Insufficiency;vertebrobasilar", "Vertebrobasilar Insufficiency", "vertebro basilar insufficiency", "a.vertebro-basilaris; syndrome", "Vertebro-basilar insufficiency", "vertebro-basilar insufficiency", "Vertebro-Basilar Insufficiency", "Insufficiency, Vertebrobasilar", "Vertebro Basilar Insufficiency", "VERTEBRAL BASILAR INSUFFICIENCY", "Vertebrobasilar Insufficiencies", "vertebral basilar insufficiency", "basilar vertebral insufficiency", "vertebrobasilar artery syndrome", "Vertebrobasilar artery syndrome", "Insufficiency, Vertebro-Basilar", "Vertebro-Basilar Insufficiencies", "Vertebro-basilar artery syndrome", "vertebro-basilar artery syndrome", "Insufficiencies, Vertebrobasilar", "Insufficiencies, Vertebro-Basilar", "syndrome; vertebro-basilar artery", "vertebrobasilar artery insufficiency", "VERTEBRAL BASILAR ARTERY INSUFFICIENCY", "Vertebrobasilar arterial insufficiency", "vertebrobasilar arterial insufficiency", "Vertebrobasilar artery syndrome (disorder)", "vertebrobasilar artery insufficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vertebrobasilar insufficiency", "shortest_name_length": 24}
{"curie": "MONDO:0005896", "names": ["Paramyxoviridae disease", "Paramyxovirus infection", "Paramyxoviridae Infection", "Infection, Paramyxoviridae", "Paramyxoviridae Infections", "Infections, Paramyxoviridae", "Paramyxovirus infection, NOS", "DISEASES DUE TO PARAMYXOVIRUS", "Disease due to Paramyxoviridae", "DISEASES DUE TO PARAMYXOVIRIDAE", "Disease caused by Paramyxoviridae", "Disease due to Paramyxovirus, NOS", "Paramyxoviridae infectious disease", "Paramyxoviridae disease or disorder", "Paramyxoviridae caused disease or disorder", "Disease caused by Paramyxoviridae (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paramyxoviridae infectious disease", "shortest_name_length": 23}
{"curie": "MONDO:0017162", "names": ["Seghers syndrome", "imperforate oropharynx-costo vetebral anomalies", "imperforate oropharynx-costo vetebral anomalies syndrome", "imperforate oropharynx-costovertebral anomalies syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "imperforate oropharynx-costo vetebral anomalies syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0000534", "names": ["trachea mucoepidermoid carcinoma", "Mucoepidermoid carcinoma of trachea", "Primary mucoepidermoid carcinoma of trachea", "Primary mucoepidermoid carcinoma of trachea (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trachea mucoepidermoid carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0010693", "names": ["NYS1", "XLPAN", "XIPAN", "Xlpan", "IIN, FORMERLY", "congenital nystagmus 1", "FRMD7 congenital nystagmus", "congenital motor nystagmus 1", "Nystagmus, congenital motor, 1", "NYSTAGMUS, CONGENITAL MOTOR, 1", "X-linked infantile nystagmus 1", "Nystagmus, infantile idiopathic", "Nystagmus 1, infantile, X-linked", "Nystagmus 1, Infantile, X-Linked", "NYSTAGMUS 1, INFANTILE, X-LINKED", "nystagmus 1, congenital, X-linked", "Nystagmus 1, Congenital, X-Linked", "NYSTAGMUS 1, congenital, X-linked", "NYSTAGMUS 1, CONGENITAL, X-LINKED", "Nystagmus 1, congenital, X- linked", "NYSTAGMUS, INFANTILE IDIOPATHIC, FORMERLY", "Nystagmus, infantile idiopathic, formerly", "congenital nystagmus caused by mutation in FRMD7", "Nystagmus, Infantile Periodic Alternating, X-Linked", "NYSTAGMUS, INFANTILE PERIODIC ALTERNATING, X-LINKED", "Nystagmus, infantile periodic alternating, X-linked", "NYSTAGMUS, INFANTILE PERIODIC ALTERNATING, X-LINKED (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nystagmus 1, congenital, X-linked", "shortest_name_length": 4}
{"curie": "MONDO:0014124", "names": ["AOS4", "Adams-Oliver syndrome 4", "ADAMS-OLIVER SYNDROME 4", "EOGT Adams-Oliver syndrome", "Adams-Oliver syndrome type 4", "Adams-Oliver syndrome caused by mutation in EOGT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adams-Oliver syndrome 4", "shortest_name_length": 4}
{"curie": "UMLS:C0021342", "names": ["Septic enteritis", "Infective enteritis", "infectious enteritis", "Enteritis infectious", "Infectious enteritis", "enteritis infectious", "Enteritis;infectious", "infectious; enteritis", "Septic enteritis, NOS", "enteritis; infectious", "Infectious enteritis NOS", "Infectious enteritis, NOS", "infectious enteritis (diagnosis)", "Infectious enteritis of intestine", "Infectious inflammation of intestine", "Infectious inflammation of intestine (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infectious enteritis", "shortest_name_length": 16}
{"curie": "MONDO:0016456", "names": ["Del(5)(q14.3)", "monosomy 5q14.3", "Monosomy 5q14.3", "5q14.3 deletion syndrome", "5q14.3 microdeletion syndrome", "chromosome 5q14.3 deletion syndrome", "5q14.3 microdeletion syndrome (disorder)", "autosomal dominant intellectual disability 20"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "5q14.3 microdeletion syndrome", "shortest_name_length": 13}
{"curie": "UMLS:C4725864", "names": ["Resectable Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Malignant Neoplasm", "shortest_name_length": 29}
{"curie": "MONDO:0002815", "names": ["acute myocarditis", "Acute myocarditis", "myocarditis acute", "Myocarditis;acute", "Acute Myocarditis", "acute; myocarditis", "myocarditis, acute", "Acute myocarditis, NOS", "Acute myocarditis (disorder)", "acute myocarditis (diagnosis)", "Acute myocarditis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myocarditis", "shortest_name_length": 17}
{"curie": "MONDO:0018327", "names": ["Glomus Tumor", "tumor glomus", "Glomus tumor", "glomus tumor", "glomus tumors", "Glomus tumour", "Glomus Tumors", "glomus tumour", "Tumor, Glomus", "Tumors, Glomus", "glomus neoplasm", "Glomus neoplasm", "Glomus Neoplasm", "Glomus tumor (disorder)", "Glomus tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glomus tumor", "shortest_name_length": 12}
{"curie": "UMLS:C0232208", "names": ["RHYTHM NODAL", "Rhythm nodal", "Nodal rhythm", "nodal rhythm", "rhythm; nodal", "nodal; rhythm", "AV NODE RHYTHMS", "Junctional Rhythm", "junctional rhythm", "Junctional rhythm", "JUNCTIONAL RHYTHM", "junctional rhythms", "AV junctional rhythm", "Junctional Rhythm by ECG Finding", "Junctional Rhythm by EKG Finding", "atrioventricular junctional rhythm", "Atrioventricular junctional rhythm", "Atrioventricular junctional rhythm (disorder)", "atrioventricular junctional rhythm (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atrioventricular junctional rhythm", "shortest_name_length": 12}
{"curie": "UMLS:C0742964", "names": ["cystitis bacterial", "CYSTITIS BACTERIAL", "Cystitis bacterial", "Bacterial cystitis", "bacterial cystitis", "Bacterial cystitis (disorder)", "Bacterial cystitis (diagnosis)", "Bladder infection due to Bacteria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bacterial cystitis", "shortest_name_length": 18}
{"curie": "MONDO:0021165", "names": ["Paget Disease", "Paget disease", "Paget's disease", "Paget's Disease", "Paget Cell Neoplasm", "Paget cell neoplasm", "Paget's cell neoplasm", "Paget's Cell Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paget disease", "shortest_name_length": 13}
{"curie": "MONDO:0100440", "names": ["Asperger syndrome, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Asperger syndrome, susceptibility to", "shortest_name_length": 36}
{"curie": "UMLS:C4764256", "names": ["Platinum-Sensitive Lung Small Cell Carcinoma", "Platinum-Sensitive Small Cell Lung Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Platinum-Sensitive Lung Small Cell Carcinoma", "shortest_name_length": 44}
{"curie": "MONDO:0006262", "names": ["lacrimal gland adenoid cystic carcinoma", "Lacrimal Gland Adenoid Cystic Carcinoma", "adenoid cystic carcinoma of lacrimal gland", "Adenoid cystic carcinoma of lacrimal gland", "Adenoid Cystic Carcinoma of Lacrimal Gland", "Adenoid Cystic Carcinoma of the Lacrimal Gland", "adenoid cystic carcinoma of the lacrimal gland", "lacrimal gland malignant carcinoma adenoid cystic", "Adenoid cystic carcinoma of lacrimal gland (disorder)", "adenoid cystic carcinoma of lacrimal gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lacrimal gland adenoid cystic carcinoma", "shortest_name_length": 39}
{"curie": "UMLS:C0854717", "names": ["Corneal epithelium disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Corneal epithelium disorder", "shortest_name_length": 27}
{"curie": "UMLS:C0152964", "names": ["streptococcemia", "STREP BACTEREMIA", "strep bacteremia", "Streptococcaemia", "streptococcal sepsis", "Streptococcal sepsis", "streptococcal; sepsis", "sepsis; streptococcal", "Streptococcal bacteremia", "septicemia streptococcal", "streptococcal septicemia", "streptococcal bacteremia", "Septicemia streptococcal", "Streptococcal septicemia", "Streptococcal septicaemia", "Septicaemia streptococcal", "streptococcal septicaemia", "Streptococcal bacteraemia", "Streptococcal sepsis, unspecified", "streptococcal bacteremia (diagnosis)", "Streptococcal septicemia (diagnosis)", "Streptococcal septicemia, unspecified", "Streptococcal septicaemia, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Streptococcal bacteremia", "shortest_name_length": 15}
{"curie": "UMLS:C5238461", "names": ["Locally Advanced Pancreatic Neuroendocrine Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Pancreatic Neuroendocrine Tumor", "shortest_name_length": 48}
{"curie": "MONDO:0044322", "names": ["IDDNPF", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH NEUROPSYCHIATRIC FEATURES", "intellectual developmental disorder with neuropsychiatric features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder with neuropsychiatric features", "shortest_name_length": 6}
{"curie": "UMLS:C4744549", "names": ["Autoimmune Atrophic Chronic Gastritis", "Autoimmune atrophic chronic gastritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Autoimmune Atrophic Chronic Gastritis", "shortest_name_length": 37}
{"curie": "UMLS:C4521753", "names": ["Stage II Gastric (Stomach) Cancer", "Clinical Stage II Gastric Cancer AJCC v8", "Clinical Stage II Gastric Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage II Gastric Cancer AJCC v8", "shortest_name_length": 33}
{"curie": "UMLS:C0857457", "names": ["digoxin effect", "digoxin effects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "digoxin effect", "shortest_name_length": 14}
{"curie": "MONDO:0003995", "names": ["childhood sarcoma Botryoides of the vulva", "childhood sarcoma Botryoides of the Vulva", "Childhood Sarcoma Botryoides of the Vulva", "Childhood Vulvar Embryonal Rhabdomyosarcoma", "mammalian vulva childhood botryoid rhabdomyosarcoma", "childhood botryoid rhabdomyosarcoma of mammalian vulva", "Vulvar Childhood Botryoid-Type Embryonal Rhabdomyosarcoma", "vulvar childhood botryoid-type embryonal rhabdomyosarcoma", "Childhood Vulvar Botryoid-Type Embryonal Rhabdomyosarcoma", "Childhood Botryoid-Type Embryonal Rhabdomyosarcoma of the Vulva", "childhood botryoid-type embryonal rhabdomyosarcoma of the vulva"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar childhood botryoid-type embryonal rhabdomyosarcoma", "shortest_name_length": 41}
{"curie": "MONDO:0008628", "names": ["Ureterocele", "ureterocele", "URETEROCELE", "ureteroceles", "Ureteroceles", "ureterocele (disease)", "Ureterocele (disorder)", "ureterocele (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ureterocele", "shortest_name_length": 11}
{"curie": "UMLS:C5555054", "names": ["FUS-NFATC2 Sarcoma", "FUS::NFATC2 Sarcoma", "Round Cell Sarcoma with FUS-NFATC2 Gene Fusion", "Round Cell Sarcoma with FUS::NFATC2 Gene Fusion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Round Cell Sarcoma with FUS-NFATC2 Gene Fusion", "shortest_name_length": 18}
{"curie": "MONDO:0014356", "names": ["MC3DN7", "UQCC2 mitochondrial complex III deficiency", "mitochondrial Complex 3 deficiency, nuclear type 7", "mitochondrial complex III deficiency nuclear type 7", "MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7", "mitochondrial complex III deficiency, nuclear type 7", "mitochondrial complex III deficiency caused by mutation in UQCC2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex III deficiency nuclear type 7", "shortest_name_length": 6}
{"curie": "UMLS:C4303267", "names": ["Primary Breast Angiosarcoma", "Primary angiosarcoma of breast", "Primary Angiosarcoma of the Breast", "Primary angiosarcoma of breast (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary angiosarcoma of breast", "shortest_name_length": 27}
{"curie": "UMLS:C1096282", "names": ["Medication residue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Medication residue", "shortest_name_length": 18}
{"curie": "UMLS:C4744849", "names": ["Refractory Kaposi Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Kaposi Sarcoma", "shortest_name_length": 25}
{"curie": "MONDO:0011198", "names": ["SEMDM", "MANDP1", "SEMD type 2", "SEMD Missouri type", "SEMD, Missouri type", "SEMD, Missouri Type", "SEMD, MISSOURI TYPE", "Metaphyseal Anadysplasia 1", "METAPHYSEAL ANADYSPLASIA 1", "metaphyseal anadysplasia 1", "spondyloepimetaphyseal dysplasia type 2", "Spondyloepimetaphyseal dysplasia type 2", "Spondyloepimetaphyseal dysplasia Missouri type", "spondyloepimetaphyseal dysplasia Missouri type", "Spondyloepimetaphyseal dysplasia, Missouri type", "SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MISSOURI TYPE", "Spondyloepimetaphyseal Dysplasia, Missouri Type", "spondyloepimetaphyseal dysplasia, Missouri type", "Missouri type of spondyloepimetaphyseal dysplasia", "Spondyloepimetaphyseal dysplasia Missouri type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepimetaphyseal dysplasia, Missouri type", "shortest_name_length": 5}
{"curie": "UMLS:C0422852", "names": ["Auditory seizure", "Auditory Seizure", "Auditory Seizures", "Seizure, Auditory", "Seizures, Auditory", "Auditory uncinate fit", "Uncinate fit, auditory", "Auditory partial seizure", "Seizure, auditory, partial", "Auditory seizure (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Seizures, Auditory", "shortest_name_length": 16}
{"curie": "UMLS:C0342142", "names": ["Jod-Basedow", "Jod-Basedow Syndrome", "Jod-Basedow phenomenon", "Jod-Basedow Phenomenon", "Jod-Basedow thyrotoxicosis", "iodine induced thyrotoxicosis", "Iodine-induced thyrotoxicosis", "Iodide-induced hyperthyroidism", "Iodine-Induced Hyperthyroidism", "Iodine-induced hyperthyroidism", "Iodine-induced hyperthyroidism, NOS", "Iodide-induced hyperthyroidism, NOS", "Iodine-induced thyrotoxicosis (disorder)", "iodine induced thyrotoxicosis (diagnosis)", "Jod Basedow iodine induced hyperthyroidism", "iodine induced thyrotoxicosis (Jod-Basedow)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Iodine-induced hyperthyroidism", "shortest_name_length": 11}
{"curie": "UMLS:C4527189", "names": ["Stage IIID Cutaneous (Skin) Melanoma", "Pathologic Stage IIID Cutaneous Melanoma AJCC v8", "Pathologic Stage IIID Melanoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IIID Cutaneous Melanoma AJCC v8", "shortest_name_length": 36}
{"curie": "MONDO:0029140", "names": ["DEE95", "GPIBD18", "early infantile epileptic encephalopathy 95", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 95", "developmental and epileptic encephalopathy 95", "GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18", "glycosylphosphatidylinositol biosynthesis defect 18"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycosylphosphatidylinositol biosynthesis defect 18", "shortest_name_length": 5}
{"curie": "MONDO:0019158", "names": ["TEMF", "Davies disease", "tropical endomyocardial fibrosis", "Tropical endomyocardial fibrosis", "Endomyocardial (tropical) fibrosis", "Tropical endomyocardial fibrosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tropical endomyocardial fibrosis", "shortest_name_length": 4}
{"curie": "UMLS:C0242341", "names": ["Sexual Infantilism", "INFANTILISM, SEXUAL", "Infantilism, Sexual"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sexual Infantilism", "shortest_name_length": 18}
{"curie": "EFO:0010638", "names": ["atopic asthma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atopic asthma", "shortest_name_length": 13}
{"curie": "UMLS:C1266149", "names": ["Neuroendocrine tumor grade 3", "Neuroendocrine tumour grade 3", "Neuroendocrine carcinoma, grade 3", "Grade III Neuroendocrine Carcinoma", "Neuroendocrine carcinoma, grade 3 (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neuroendocrine tumor grade 3", "shortest_name_length": 28}
{"curie": "DOID:4661", "names": ["chemical AIDS", "20th century disease", "environmental illness", "total allergy syndrome", "Multiple Chemical Sensitivity", "Multiple chemical sensitivity", "multiple chemical sensitivity", "chemical multiple sensitivity", "Sensitivity, Multiple Chemical", "chemicals multiple sensitivity", "Chemical Sensitivity, Multiple", "Multiple Chemical Sensitivities", "multiple chemical sensitivities", "Sensitivities, Multiple Chemical", "idiopathic environmental illness", "Chemical Sensitivities, Multiple", "Idiopathic environmental intolerance", "Idiopathic Environmental Intolerance", "Intolerance, Idiopathic Environmental", "Idiopathic Environmental Intolerances", "Environmental Intolerance, Idiopathic", "Multiple Chemical Sensitivity Syndrome", "Environmental Intolerances, Idiopathic", "Intolerances, Idiopathic Environmental", "Idiopathic environmental intolerance (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple chemical sensitivity", "shortest_name_length": 13}
{"curie": "MONDO:0033683", "names": ["MYSM1 deficiency", "congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0011821", "names": ["MKS3", "Meckel syndrome 3", "Meckel syndrome type 3", "TMEM67 Meckel syndrome", "Meckel syndrome, type 3", "Meckel Syndrome, Type 3", "MECKEL SYNDROME, TYPE 3", "Meckel-Gruber Syndrome, Type 3", "MECKEL-GRUBER SYNDROME, TYPE 3", "Meckel-Gruber syndrome, type 3", "Meckel syndrome type 3 (diagnosis)", "Meckel syndrome caused by mutation in TMEM67"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meckel syndrome, type 3", "shortest_name_length": 4}
{"curie": "MONDO:0019388", "names": ["pelvis syndrome", "SACRAL syndrome", "LUMBAR syndrome", "PELVIS syndrome", "urorectal septum malformation sequence", "perineal hemangioma-external genitalia malformations-lipomyelomeningocele-vesicorenal abnormalities-imperforate anus syndrome", "Perineal hemangioma, external genitalia malformation, lipomyelomeningocele, vesicorenal abnormality, imperforate anus syndrome", "Perineal haemangioma, external genitalia malformation, lipomyelomeningocele, vesicorenal abnormality, imperforate anus syndrome", "Lower body hemangioma-urogenital anomalies-myelopathy-bony deformities-anorectal and arterial malformations-renal anomalies syndrome", "Perineal hemangioma-external genitalia malformations-lipomyelomeningocele-vesicorenal abnormalities-imperforate anus-skin tag syndrome", "PELVIS (perineal hemangioma, external genitalia malformation, lipomyelomeningocele, vesicorenal abnormality, imperforate anus) syndrome", "PELVIS (Perineal haemangioma, external genitalia malformation, lipomyelomeningocele, vesicorenal abnormality, imperforate anus) syndrome", "Perineal hemangioma, external genitalia malformation, lipomyelomeningocele, vesicorenal abnormality, imperforate anus syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pelvis syndrome", "shortest_name_length": 15}
{"curie": "UMLS:C0751252", "names": ["Sleep Initiation Dysfunction", "Dysfunction, Sleep Initiation", "Sleep Initiation Dysfunctions", "Dysfunctions, Sleep Initiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sleep Initiation Dysfunction", "shortest_name_length": 28}
{"curie": "UMLS:C1698976", "names": ["Infusion site hives", "Infusion site urticaria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infusion site urticaria", "shortest_name_length": 19}
{"curie": "MONDO:0016779", "names": ["KOS", "Kagami-Ogata syndrome", "MCA due to 14q32.2 maternally expressed gene defect", "multiple congenital anomalies due to 14q32.2 maternally expressed gene defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple congenital anomalies due to 14q32.2 maternally expressed gene defect", "shortest_name_length": 3}
{"curie": "UMLS:C0877119", "names": ["cmv esophagitis", "ESOPHAGITIS CMV", "CMV Esophagitis", "cytomegalovirus esophagitis", "Cytomegalovirus Esophagitis", "Cytomegalovirus esophagitis", "Cytomegalovirus oesophagitis", "Esophagitis caused by Cytomegalovirus", "Oesophagitis caused by Cytomegalovirus", "cytomegalovirus esophagitis (diagnosis)", "Esophagitis caused by Cytomegalovirus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophagitis caused by Cytomegalovirus", "shortest_name_length": 15}
{"curie": "UMLS:C2987499", "names": ["Stage IV Penile Cancer", "stage IV penile cancer", "Stage IV Penile Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Penile Cancer AJCC v7", "shortest_name_length": 22}
{"curie": "UMLS:C4744364", "names": ["Sellar Neurocytoma", "Sellar Neurocytoma (WHO Grade 2)", "Sellar Neurocytoma (WHO Grade II)", "Extraventricular Neurocytoma of the Sellar Region", "Extraventricular Neurocytoma of the Sellar Region (WHO Grade 2)", "Extraventricular Neurocytoma of the Sellar Region (WHO Grade II)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sellar Neurocytoma", "shortest_name_length": 18}
{"curie": "MONDO:0004929", "names": ["Constant exophthalmos", "constant exophthalmos", "Constant exophthalmos (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "constant exophthalmos", "shortest_name_length": 21}
{"curie": "UMLS:C3274515", "names": ["Severe BPD", "Severe Bronchopulmonary Dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Severe Bronchopulmonary Dysplasia", "shortest_name_length": 10}
{"curie": "MONDO:0024570", "names": ["HRPT4", "HYPERPARATHYROIDISM 4", "hyperparathyroidism 4", "hyperparathyroidism type 4", "GCM2 familial isolated hyperparathyroidism", "familial isolated hyperparathyroidism caused by mutation in GCM2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperparathyroidism 4", "shortest_name_length": 5}
{"curie": "UMLS:C4285866", "names": ["Serous Fat Atrophy", "SEROUS ATROPHY OF FAT", "Gelatinous Bone Marrow Transformation", "Gelatinous transformation of the bone marrow"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gelatinous transformation of the bone marrow", "shortest_name_length": 18}
{"curie": "UMLS:C1336351", "names": ["Stage IVA Mouth Carcinoma", "Stage IVA Carcinoma of Mouth", "Stage IVA Oral Cavity Cancer", "Stage IVA Oral Cavity Carcinoma", "Stage IVA Carcinoma of the Mouth", "Stage IVA Carcinoma of Oral Cavity", "Stage IVA Oral Cavity Cancer AJCC v7", "Stage IVA Oral Cavity Cancer AJCC v6", "Stage IVA Carcinoma of the Oral Cavity", "Stage IVA Oral Cavity Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Oral Cavity Cancer AJCC v6 and v7", "shortest_name_length": 25}
{"curie": "UMLS:C3274275", "names": ["TAPVR Type II", "Type II Total Anomalous Pulmonary Venous Return", "Type II (Intracardiac) Total Anomalous Pulmonary Venous Return", "Total Anomalous Pulmonary Venous Return, Type II (Intracardiac)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Type II Total Anomalous Pulmonary Venous Return", "shortest_name_length": 13}
{"curie": "UMLS:C1333995", "names": ["Hernia with Obstruction without Mention of Gangrene"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hernia with Obstruction without Mention of Gangrene", "shortest_name_length": 51}
{"curie": "MONDO:0008592", "names": ["TDO", "TDO SYNDROME", "TDO syndrome", "TDO syndrome 1", "TRICHODENTOOSSEOUS SYNDROME", "Trichodentoosseous Syndrome", "TRICHODENTOOSSEOUS syndrome", "trichodontoosseous syndrome", "Trichodento-osseous syndrome", "Tricho-dento-osseous syndrome", "tricho-dento-osseous syndrome", "Tricho-dento-osseous syndrome 1", "TDO - Trichodento-osseous syndrome", "Tricho-dento-osseous syndrome (disorder)", "Amelogenesis imperfecta - osteosclerosis syndrome", "Taurodontism - curly hair - osteosclerosis syndrome", "enamel hypoplasia and hypocalcification with associated strikingly curly hair", "kinky or curly hair, dolichocephaly, enamel hypoplasia, increased dental caries, radial dense bones, and brittle nails"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tricho-dento-osseous syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0016544", "names": ["mesenteric panniculitis", "sclerosing mesenteritis", "lipomatous mesenteritis", "mesenteric lipogranuloma", "IgG4-related mesenteritis", "liposclerotic mesenteritis", "isolated mesenteric lipodystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IgG4-related mesenteritis", "shortest_name_length": 23}
{"curie": "EFO:0004229", "names": ["Dupuytren Contracture"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dupuytren Contracture", "shortest_name_length": 21}
{"curie": "MONDO:0001262", "names": ["African Histoplasmosis", "African histoplasmosis", "HISTOPLASMOSIS, AFRICAN", "Histoplasmosis duboisii", "histoplasmosis; African", "Histoplasmosis, African", "African; histoplasmosis", "large form histoplasmosis", "Large form histoplasmosis", "Histoplasma duboisii infection", "Histoplasma duboisii Infection", "Infection, Histoplasma duboisii", "Histoplasma duboisii Infections", "Infection by Histoplasma duboisii", "African histoplasmosis (disorder)", "infection by Histoplasma duboisii", "Histoplasma duboisii; histoplasmosis", "histoplasmosis; Histoplasma duboisii", "histoplasmosis due to Histoplasma duboisii", "histoplasmosis due to Histoplasma duboisii (diagnosis)", "Histoplasma capsulatum var. duboisii infectious disease", "Histoplasma capsulatum var. duboisii disease or disorder", "Histoplasma capsulatum var. duboisii caused disease or disorder", "Infection by Histoplasma duboisii, without mention of manifestation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "African histoplasmosis", "shortest_name_length": 22}
{"curie": "MONDO:0006317", "names": ["neurothecoma", "Neurothecoma", "Neurotheceoma", "neurothekeoma", "Neurothecomas", "Neurothekeoma", "Neurothekeomas", "Neurotheceomas", "[M] Neurothekeoma", "Lobular neuromyxoma", "nerve sheath myxoma", "Nerve Sheath Myxoma", "nerve sheath Myxoma", "Nerve sheath myxoma", "Nerve Sheath Myxomas", "Myxoma, Nerve Sheath", "Myxomas, Nerve Sheath", "Neurothekeoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurothekeoma", "shortest_name_length": 12}
{"curie": "UMLS:C0343886", "names": ["Moniliasis GI", "MONILIASIS GI", "GI candidiasis", "gi candidiasis", "candidal enteritis", "intestinal moniliasis", "intestinal candidiasis", "Gastrointestinal candida", "gastrointestinal candida", "Candidiasis of intestine", "Gastrointestinal moniliasis", "Moniliasis gastrointestinal", "GASTROINTESTINAL MONILIASIS", "MONILIASIS GASTROINTESTINAL", "Gastrointestinal candidiasis", "gastrointestinal candidiasis", "Candidiasis of the intestine", "Gastro-intestinal candidiasis", "Gastrointestinal candidiasis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal candidiasis", "shortest_name_length": 13}
{"curie": "UMLS:C4552934", "names": ["Stage II Fallopian Tube Cancer", "Stage II Fallopian Tube Cancer AJCC v8", "Stage II Fallopian Tube Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Fallopian Tube Cancer AJCC v8", "shortest_name_length": 30}
{"curie": "MONDO:0035774", "names": ["NRXN1-related severe neurodevelopmental disorder-motor stereotypies-chronic constipation-sleep-wake cycle disturbance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "NRXN1-related severe neurodevelopmental disorder-motor stereotypies-chronic constipation-sleep-wake cycle disturbance", "shortest_name_length": 117}
{"curie": "MONDO:0002149", "names": ["reproductive tumor", "Reproductive tumor", "reproductive organ cancer", "reproductive system cancer", "cancer of reproductive organ", "cancer of reproductive system", "malignant reproductive organ neoplasm", "Malignant Reproductive System Neoplasm", "malignant reproductive system neoplasm", "malignant neoplasm of reproductive organ", "malignant neoplasm of reproductive system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "reproductive system cancer", "shortest_name_length": 18}
{"curie": "MONDO:0044785", "names": ["Desmoplastic Melanoma", "Desmoplastic melanoma", "desmoplastic melanoma", "desmoplastic cutaneous (skin) melanoma", "Desmoplastic Cutaneous (Skin) Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "desmoplastic melanoma", "shortest_name_length": 21}
{"curie": "MONDO:0020581", "names": ["Benign PEComa", "benign PEComa", "Typical PEComa", "typical PEComa", "PEComa, benign", "benign PEComa, nos", "Benign PEComa, NOS", "benign PEComa, not otherwise specified", "Perivascular epithelioid tumor, benign", "Benign PEComa, Not Otherwise Specified", "Perivascular epithelioid tumour, benign", "Perivascular epithelioid tumor, benign (morphologic abnormality)", "benign neoplasm with perivascular epithelioid cell differentiation", "neoplasm with perivascular epithelioid cell differentiation, benign"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign PEComa", "shortest_name_length": 13}
{"curie": "MONDO:0019845", "names": ["iatrogenic or traumatic pituitary deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "iatrogenic or traumatic pituitary deficiency", "shortest_name_length": 44}
{"curie": "UMLS:C1698039", "names": ["anastomotic leak fallopian tube", "Fallopian tube anastomotic leak", "Fallopian Tube Anastomotic Leakage", "anastomotic leak of fallopian tube", "anastomotic leak of fallopian tube (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fallopian Tube Anastomotic Leakage", "shortest_name_length": 31}
{"curie": "MONDO:0016988", "names": ["Hyperinsulinism due to HNF4A deficiency", "hyperinsulinism due to HNF4A deficiency", "hyperinsulinemic hypoglycemia due to HNF4A deficiency", "Hyperinsulinemic hypoglycemia due to HNF4A deficiency", "Hyperinsulinism due to hepatocyte nuclear factor 4-alpha deficiency", "Hyperinsulinism due to hepatocyte nuclear factor 4-alpha deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperinsulinism due to HNF4A deficiency", "shortest_name_length": 39}
{"curie": "OMIM:614401", "names": ["ACTFS", "ACCELERATED TUMOR FORMATION, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 5}
{"curie": "MONDO:0009415", "names": ["LIH", "hypoglycemia; leucine", "leucine; hypoglycemia", "hypoglycemia leucine-induced", "Leucine-induced hypoglycemia", "leucine-induced hypoglycemia", "hypoglycemia leucine induced", "hypoglycemia, leucine-induced", "Hypoglycemia, leucine-induced", "HYPOGLYCEMIA, LEUCINE-INDUCED", "Leucine-induced hypoglycaemia", "Leucine-induced hypoglycemia (disorder)", "leucine-sensitive hypoglycemia of infancy", "Leucine-sensitive hypoglycemia of infancy", "LEUCINE-SENSITIVE HYPOGLYCEMIA OF INFANCY", "hypoglycemia of infancy, leucine-sensitive", "familial infantile hypoglycemia precipitated by leucine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypoglycemia, leucine-induced", "shortest_name_length": 3}
{"curie": "UMLS:C5418788", "names": ["Metastatic Rectal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Rectal Squamous Cell Carcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0014943", "names": ["MTDPS15", "mitochondrial DNA depletion syndrome 15", "TFAM mitochondrial DNA depletion syndrome", "mitochondrial DNA depletion syndrome 15 (hepatocerebral type)", "MITOCHONDRIAL DNA DEPLETION SYNDROME 15 (HEPATOCEREBRAL TYPE)", "mitochondrial DNA depletion syndrome caused by mutation in TFAM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial DNA depletion syndrome 15 (hepatocerebral type)", "shortest_name_length": 7}
{"curie": "MONDO:0000912", "names": ["NSRD5", "DFNB5", "autosomal recessive deafness 5", "deafness, autosomal recessive 5", "DEAFNESS, AUTOSOMAL RECESSIVE 5", "Deafness, Autosomal Recessive 5", "DEAFNESS, AUTOSOMAL RECESSIVE 5 (disorder)", "autosomal recessive nonsyndromic deafness 5", "NEUROSENSORY NONSYNDROMIC RECESSIVE DEAFNESS 5", "neurosensory nonsyndromic recessive deafness 5", "Neurosensory Nonsyndromic Recessive Deafness 5", "autosomal recessive nonsyndromic hearing loss 5", "autosomal recessive nonsyndromic deafness type 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 5", "shortest_name_length": 5}
{"curie": "MONDO:0017034", "names": ["secondary ILD in childhood and adulthood", "secondary interstitial lung disease in childhood and adulthood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary interstitial lung disease in childhood and adulthood", "shortest_name_length": 40}
{"curie": "MONDO:0023726", "names": ["EST", "mediastinal yolk Sac tumor", "mediastinal yolk sac tumor", "mediastinum yolk sac tumor", "Mediastinal Yolk Sac Tumor", "yolk Sac tumor of mediastinum", "yolk sac tumor of mediastinum", "mediastinal yolk Sac neoplasm", "Mediastinal Yolk Sac Neoplasm", "Yolk Sac Tumor of Mediastinum", "yolk Sac neoplasm of mediastinum", "Yolk Sac Neoplasm of Mediastinum", "yolk Sac tumor of the mediastinum", "Yolk Sac Tumor of the Mediastinum", "mediastinal endodermal sinus tumor", "Mediastinal Endodermal Sinus Tumor", "mediastinal endodermal sinus tumors", "Yolk Sac Neoplasm of the Mediastinum", "yolk Sac neoplasm of the mediastinum", "endodermal sinus tumor of mediastinum", "Mediastinal Endodermal Sinus Neoplasm", "Endodermal Sinus Tumor of Mediastinum", "mediastinal endodermal sinus neoplasm", "Endodermal Sinus Neoplasm of Mediastinum", "endodermal sinus neoplasm of mediastinum", "yolk sac tumor of mediastinum (diagnosis)", "Endodermal Sinus Tumor of the Mediastinum", "endodermal sinus tumor of the mediastinum", "endodermal sinus neoplasm of the mediastinum", "Endodermal Sinus Neoplasm of the Mediastinum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mediastinal yolk sac tumor", "shortest_name_length": 3}
{"curie": "UMLS:C0263852", "names": ["Spinal arthritis deformans", "spinal arthritis deformans", "Spinal arthritis, deformans", "degenerative spine arthritis", "Degenerative arthritis spine", "arthritis degenerative spine", "degenerative arthritis spine", "spinal hypertrophic arthritis", "degenerative spinal arthritis", "spinal degenerative arthritis", "Degenerative spinal arthritis", "Hypertrophic spinal arthritis", "Spinal Degenerative Arthritis", "Spinal arthritis, hypertrophic", "Spinal arthritis, degenerative", "Spinal arthritis deformans (disorder)", "spinal arthritis deformans (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spinal arthritis deformans", "shortest_name_length": 26}
{"curie": "MONDO:0004098", "names": ["Mediastinal Melanocytic MPNST", "mediastinal melanocytic MPNST", "Malignant Mediastinal Melanocytic Peripheral Nerve Sheath Tumor", "malignant mediastinal melanocytic peripheral nerve sheath tumor", "malignant melanocytic peripheral nerve sheath tumor of mediastinum", "Malignant Melanocytic Peripheral Nerve Sheath Tumor of Mediastinum", "Malignant Melanotic Peripheral Nerve Sheath Tumor of the Mediastinum", "malignant melanotic peripheral nerve sheath tumor of the mediastinum", "mediastinum malignant melanocytic neoplasm of the peripheral nerve sheath", "malignant melanocytic neoplasm of the peripheral nerve sheath of mediastinum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant melanocytic peripheral nerve sheath tumor of mediastinum", "shortest_name_length": 29}
{"curie": "MONDO:0018270", "names": ["EOE", "Extraosseous Ewing tumor", "extraosseous Ewing tumor", "Extraskeletal Ewing tumor", "extraskeletal Ewing tumor", "Extraosseous Ewing sarcoma", "Extraosseous Ewing's Tumor", "extraosseous Ewing's tumor", "extraskeletal Ewing sarcom", "extraosseous Ewing sarcoma", "Extraosseous Ewing Sarcoma", "Extraskeletal Ewing Sarcoma", "Extraskeletal Ewing sarcoma", "extraskeletal Ewing sarcoma", "extraosseous Ewing's sarcoma", "extraosseous ewing's sarcoma", "Extraosseous Ewing's Sarcoma", "Extra-Osseous Ewing's Sarcoma", "Extra-osseous Ewing's sarcoma", "Extraskeletal Ewing's Sarcoma", "extraskeletal Ewing's sarcoma", "Extraskeletal Ewing's sarcomas", "extraosseous Ewing tumor (EOE)", "Extra-osseous Ewing's sarcoma NOS", "extraosseous Ewing's sarcoma/peripheral primitive neuroectodermal tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extraskeletal Ewing sarcoma", "shortest_name_length": 3}
{"curie": "UMLS:C0221047", "names": ["Brady-tachy syndrome", "BRADY-TACHY SYNDROME", "tachy-brady syndrome", "brady-tachy syndrome", "Tachycardia-bradycardia", "tachycardia bradycardia", "BRADYCARDIA-TACHYCARDIA SYNDROME", "bradycardia tachycardia syndrome", "tachycardia-bradycardia syndrome", "Tachycardia bradycardia syndrome", "bradycardia-tachycardia syndrome", "Bradycardia-tachycardia syndrome", "Tachycardia-bradycardia syndrome", "syndrome; tachycardia-bradycardia", "tachycardia-bradycardia; syndrome", "Syndrome, tachycardia-bradycardia", "Tachycardia-bradycardia (disorder)", "Tachycardia-bradycardia (diagnosis)", "bradyarrhythmia tachycardia-bradycardia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bradycardia-tachycardia syndrome", "shortest_name_length": 20}
{"curie": "MONDO:0007323", "names": ["Chondronectin", "CHONDRONECTIN", "CHONDRONECTIN PHENOTYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chondronectin", "shortest_name_length": 13}
{"curie": "UMLS:C4528671", "names": ["II", "Stage II Hepatocellular Cancer", "Stage II Liver Cell Carcinoma AJCC v8", "Stage II Hepatocellular Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Hepatocellular Carcinoma AJCC v8", "shortest_name_length": 2}
{"curie": "UMLS:C3897661", "names": ["Sacral Fistula"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sacral Fistula", "shortest_name_length": 14}
{"curie": "MONDO:0015451", "names": ["Univentricular Heart", "univentricular heart", "Double-inlet left ventricle", "double inlet left ventricle", "Double inlet left ventricle", "double inlet ventricle LV type", "DILV - Double inlet left ventricle", "Double inlet left ventricle (disorder)", "double inlet left ventricle (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "univentricular heart", "shortest_name_length": 20}
{"curie": "UMLS:C0521795", "names": ["Ectopic Prolactin Secretion", "Ectopic prolactin secretion", "Ectopic Prolactin Secretion Syndrome", "Ectopic prolactin secretion (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ectopic prolactin secretion", "shortest_name_length": 27}
{"curie": "MONDO:0013761", "names": ["THMD5", "childhood encephalopathy due to thiamine pyrophosphokinase deficiency", "encephalopathy, episodic, due to thiamine pyrophosphokinase deficiency", "ENCEPHALOPATHY, EPISODIC, DUE TO THIAMINE PYROPHOSPHOKINASE DEFICIENCY", "thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)", "THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood encephalopathy due to thiamine pyrophosphokinase deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0016123", "names": ["muscular tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular tumor", "shortest_name_length": 14}
{"curie": "UMLS:C4521640", "names": ["Stage IIA Esophageal Adenocarcinoma", "Clinical Stage IIA Esophageal Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage IIA Esophageal Adenocarcinoma AJCC v8", "shortest_name_length": 35}
{"curie": "UMLS:C5555765", "names": ["HER2-Low Breast Carcinoma", "HER2 Low Breast Carcinoma", "HER2-Low Breast Adenocarcinoma", "HER2 Low Breast Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HER2-Low Breast Carcinoma", "shortest_name_length": 25}
{"curie": "UMLS:C4744462", "names": ["Refractory Digestive System Neuroendocrine Carcinoma", "Refractory Gastrointestinal System Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Digestive System Neuroendocrine Carcinoma", "shortest_name_length": 52}
{"curie": "UMLS:C3899505", "names": ["Congenital Disruption"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Disruption", "shortest_name_length": 21}
{"curie": "UMLS:C3272764", "names": ["Appendix Low Grade Dysplasia", "Appendiceal Low Grade Dysplasia", "Appendix Low Grade Intraepithelial Neoplasia", "Appendiceal Low Grade Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Appendix Low Grade Intraepithelial Neoplasia", "shortest_name_length": 28}
{"curie": "MONDO:0004397", "names": ["Mediastinal Psammomatous Schwannoma", "Benign Mediastinal Psammomatous Schwannoma", "benign mediastinal psammomatous schwannoma", "benign mediastinal psammomatous neurilemmoma", "Benign Mediastinal Psammomatous Neurilemmoma", "benign Psammomatous Schwannoma of mediastinum", "benign psammomatous schwannoma of mediastinum", "Benign Psammomatous Schwannoma of Mediastinum", "benign psammomatous neurilemmoma of mediastinum", "Benign Psammomatous Neurilemmoma of Mediastinum", "Benign Psammomatous Schwannoma of the Mediastinum", "benign psammomatous schwannoma of the mediastinum", "benign psammomatous neurilemmoma of the mediastinum", "Benign Psammomatous Neurilemmoma of the Mediastinum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign mediastinal psammomatous neurilemmoma", "shortest_name_length": 35}
{"curie": "MONDO:0010548", "names": ["SCAX2", "Scax2", "X-linked spinocerebellar ataxia 2", "Spinocerebellar Ataxia, X-Linked 2", "SPINOCEREBELLAR ATAXIA, X-LINKED 2", "spinocerebellar ataxia, X-linked 2", "Spinocerebellar ataxia, X-linked, 2", "spinocerebellar ataxia X-linked type 2", "spinocerebellar ataxia, X-linked type 2", "cerebellar ataxia with extrapyramidal involvement early-onset", "CEREBELLAR ATAXIA WITH EXTRAPYRAMIDAL INVOLVEMENT, EARLY-ONSET", "Cerebellar ataxia with extrapyramidal involvement, early-onset", "cerebellar ataxia with extrapyramidal involvement, early-onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia, X-linked 2", "shortest_name_length": 5}
{"curie": "MONDO:0008498", "names": ["STBMS1", "STRABISMUS, SUSCEPTIBILITY TO", "strabismus, susceptibility to", "STRABISMUS, SUSCEPTIBILITY TO, 1", "strabismus, susceptibility to, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "strabismus, susceptibility to", "shortest_name_length": 6}
{"curie": "MONDO:0015544", "names": ["acquired hemophagocytic lymphohistiocytosis associated with malignant disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired hemophagocytic lymphohistiocytosis associated with malignant disease", "shortest_name_length": 77}
{"curie": "MONDO:0010920", "names": ["M-A", "anotia", "MICROTIA", "microtia", "Microtia", "Microtias", "Small ears", "Small pinnae", "microtia-anotia", "Microtia-Anotia", "MICROTIA-ANOTIA", "Hypoplastic ears", "Hypoplastic pinna", "Hypoplastic pinnae", "Bilateral microtia", "microtia was noted", "Underdeveloped ears", "Microtia, bilateral", "Microtia (disorder)", "Congenital Microtia", "Microtia, Congenital", "microtia (diagnosis)", "microtia, congenital", "Congenital Microtias", "congenital microtias", "Microtias, Congenital", "Congenital small ears", "microtias, congenital", "microtia (physical finding)", "Hypoplasia of the external ear", "ear auricle malformations microtia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microtia", "shortest_name_length": 3}
{"curie": "UMLS:C1334466", "names": ["Lymphomatous Adult T-Cell Leukemia/Lymphoma", "Lymphomatous Adult T-Cell Lymphoma/Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphomatous Adult T-Cell Leukemia/Lymphoma", "shortest_name_length": 43}
{"curie": "UMLS:C0280605", "names": ["Brain tumor, child: PNET", "childhood supratentorial PNET", "Childhood Supratentorial PNET", "pediatric supratentorial PNET", "PNET, childhood supratentorial", "PNET, pediatric supratentorial", "PNET, supratentorial, childhood", "PNET, supratentorial, pediatric", "Supratentorial Embryonal Tumor, NOS", "Childhood Supratentorial Embryonal Tumor, NOS", "Childhood Supratentorial Primitive Neuroectodermal Tumor", "childhood supratentorial primitive neuroectodermal tumor", "pediatric supratentorial primitive neuroectodermal tumor", "primitive neuroectodermal tumor, pediatric supratentorial", "childhood primitive neuroectodermal tumor, supratentorial", "pediatric primitive neuroectodermal tumor, supratentorial", "supratentorial primitive neuroectodermal tumor, childhood", "supratentorial primitive neuroectodermal tumor, pediatric", "primitive neuroectodermal tumor, childhood supratentorial", "primitive neuroectodermal tumor, supratentorial, pediatric", "primitive neuroectodermal tumor, supratentorial, childhood", "neuroectodermal tumor, childhood, primitive, supratentorial", "neuroectodermal tumor, pediatric, primitive, supratentorial", "Childhood Supratentorial Embryonal Tumor, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Supratentorial Embryonal Tumor, Not Otherwise Specified", "shortest_name_length": 24}
{"curie": "UMLS:C5446578", "names": ["Conjunctival Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conjunctival Sarcoma", "shortest_name_length": 20}
{"curie": "MONDO:0000577", "names": ["anemia congenital", "Congenital anemia", "congenital anemia", "Congenital Anemia", "anemia; congenital", "congenital anaemia", "Anaemia;congenital", "Congenital anaemia", "congenital; anemia", "Anemia, congenital", "Congenital anemia NOS", "Congenital anemia, NOS", "Congenital anaemia NOS", "Congenital anaemia, NOS", "congenital anemia (disease)", "Congenital anemia (disorder)", "congenital anemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital anemia", "shortest_name_length": 17}
{"curie": "UMLS:C2981415", "names": ["Stage I Small Intestinal Gastrointestinal Stromal Tumor", "Stage I Small Intestinal Gastrointestinal Stromal Tumor (GIST)", "Stage I Small Intestinal Gastrointestinal Stromal Tumor AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Small Intestinal Gastrointestinal Stromal Tumor", "shortest_name_length": 55}
{"curie": "UMLS:C4745179", "names": ["Adrenal Gland Schwannoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adrenal Gland Schwannoma", "shortest_name_length": 24}
{"curie": "MONDO:0019194", "names": ["focal lipodystrophy", "Focal Lipodystrophy", "localized lipodystrophy", "Localized lipodystrophy", "Localised lipodystrophy", "Localized Lipodystrophy", "Localized lipodystrophy (disorder)", "centrifugal lipodystrophy (subtype)", "idiopathic localized lipodystrophy (subtype)", "drug-induced localized lipodystrophy (subtype)", "pressure-induced localized lipoatrophy (subtype)", "panniculitis and localized lipodystrophy (subtype)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "localized lipodystrophy", "shortest_name_length": 19}
{"curie": "UMLS:C4725662", "names": ["Advanced Oropharyngeal Squamous Cell Carcinoma", "Advanced Squamous Cell Carcinoma of the Oropharynx", "Advanced Oropharyngeal Throat Squamous Cell Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Oropharyngeal Squamous Cell Carcinoma", "shortest_name_length": 46}
{"curie": "MONDO:0000924", "names": ["compensatory emphysema", "Compensatory emphysema", "emphysema; compensatory", "compensatory; emphysema", "Compensatory emphysema (disorder)", "compensatory emphysema (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "compensatory emphysema", "shortest_name_length": 22}
{"curie": "MONDO:0007847", "names": ["KLDF", "Keloid formation", "KELOID FORMATION", "keloid formation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keloid formation", "shortest_name_length": 4}
{"curie": "UMLS:C1883714", "names": ["Warthin's tumor", "Warthin's tumour", "Parotid Gland Adenolymphoma", "Parotid Gland Warthin Tumor", "Parotid Gland Warthin's Tumor", "Warthin tumor of parotid gland", "Adenolymphoma of parotid gland", "Warthin tumour of parotid gland", "Warthin's tumor of parotid gland", "Warthin's tumour of parotid gland", "Adenolymphoma of parotid gland (disorder)", "Parotid Gland Papillary Cystadenoma Lymphomatosum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parotid Gland Warthin Tumor", "shortest_name_length": 15}
{"curie": "MONDO:0014453", "names": ["IMD36", "APDS2", "IMMUNODEFICIENCY 36", "Immunodeficiency 36", "immunodeficiency 36", "immunodeficiency type 36", "Activated PI3K-Delta Syndrome 2", "PIK3R1-Associated Immunodeficiency", "activated phosphoinositide 3-kinase delta syndrome 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 36", "shortest_name_length": 5}
{"curie": "MONDO:0031447", "names": ["macrothrombocytopenia, isolated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macrothrombocytopenia, isolated", "shortest_name_length": 31}
{"curie": "MONDO:0011795", "names": ["Teebi Kaurah syndrome", "Teebi-Kaurah syndrome", "anonychia-microcephaly syndrome", "Anonychia-microcephaly syndrome", "anonychia total with microcephaly", "total anonychia with microcephaly", "Anonychia, Total, with Microcephaly", "anonychia, total, with microcephaly", "ANONYCHIA, TOTAL, WITH MICROCEPHALY", "Anonychia with microcephaly syndrome", "total anonychia congenita and microcephaly", "Anonychia with microcephaly syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anonychia-microcephaly syndrome", "shortest_name_length": 21}
{"curie": "UMLS:C0854837", "names": ["Angiocentric lymphoma stage III", "Nasal T-cell lymphoma stage III", "Stage III Angiocentric Lymphoma", "Angiocentric Lymphoma Stage III", "Polymorphic reticulosis stage III", "Stage III Nasal Type NK/T-Cell Lymphoma", "Ann Arbor Stage III Nasal Type NK/T-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Angiocentric lymphoma stage III", "shortest_name_length": 31}
{"curie": "UMLS:C4524188", "names": ["ISFN", "FLIS", "Follicular Lymphoma In Situ", "In Situ Follicular Lymphoma", "In situ follicular lymphoma", "In Situ Follicular Neoplasia", "In situ follicular neoplasia", "ISFN - in situ follicular neoplasia", "In situ follicular neoplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "In situ follicular neoplasia", "shortest_name_length": 4}
{"curie": "MONDO:0010583", "names": ["X-linked Dyggve-Melchior-Clausen disease", "Dyggve-Melchior-Clausen syndrome X linked", "X-linked Dyggve-Melchior-Clausen syndrome", "Dyggve-Melchior-Clausen disease, X-linked", "Dyggve-Melchior-Clausen Syndrome, X-Linked", "Dyggve-Melchior-Clausen syndrome, X-linked", "DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dyggve-Melchior-Clausen syndrome, X-linked", "shortest_name_length": 40}
{"curie": "UMLS:C2116059", "names": ["Thyroid Gland Follicular Lymphoma", "follicular lymphoma of thyroid gland", "follicular lymphoma of thyroid gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "follicular lymphoma of thyroid gland", "shortest_name_length": 33}
{"curie": "UMLS:C5420074", "names": ["Sinonasal Ameloblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Ameloblastoma", "shortest_name_length": 23}
{"curie": "MONDO:0001243", "names": ["DIC", "D.I.C.", "DIC syndrome", "DIC SYNDROME", "defibrination", "DEFIBRINATION SYNDROME", "Defibrination syndrome", "defibrination syndrome", "defibrination; syndrome", "syndrome; defibrination", "CONSUMPTION COAGULOPATHY", "Consumption coagulopathy", "consumption coagulopathy", "consumptive coagulopathy", "Consumptive Coagulopathy", "Consumption Coagulopathy", "Consumptive coagulopathy", "Coagulopathy, Consumption", "coagulopathy; consumption", "Consumption Coagulopathies", "Coagulopathies, Consumption", "Hemorrhagic fibrinogenolysis", "hemorrhage; fibrinogenolysis", "fibrinogenolysis; hemorrhage", "Disseminated intravascul coag", "Haemorrhagic fibrinogenolysis", "DISSEM. INTRAVASC. COAGULATION", "defibrination syndrome (diagnosis)", "Disseminated Intravascular Coagulation", "Intravascular Disseminated Coagulation", "disseminated intravascular coagulation", "DISSEMINATED INTRAVASCULAR COAGULATION", "Disseminated intravascular coagulation", "Coagulation, Intravascular Disseminated", "Disseminated Intravascular Coagulations", "Intravascular Disseminated Coagulations", "Disseminated Coagulation, Intravascular", "Intravascular Coagulation, Disseminated", "Coagulation, Disseminated Intravascular", "Consumptive thrombohemorrhagic disorder", "Consumptive thrombohaemorrhagic disorder", "Coagulations, Disseminated Intravascular", "Coagulations, Intravascular Disseminated", "Intravascular Coagulations, Disseminated", "Disseminated Coagulations, Intravascular", "DIC, disseminated intravascular coagulation", "disseminated intravascular coagulation (DIC)", "DIC - Disseminated intravascular coagulation", "Disseminated Intravascular Coagulation (DIC)", "Consumptive thrombohemorrhagic disorder, NOS", "DIC (disseminated intravascular coagulation)", "intravascular coagulation (DIC), disseminated", "Disseminating intravascular coagulation (DIC)", "coagulation (DIC), disseminated intravascular", "Diffuse or disseminated intravascular coagulation", "diffuse or disseminated intravascular coagulation", "Disseminated intravascular coagulation (disorder)", "Disseminated intravascular coagulation (DIC) syndrome", "disseminated intravascular coagulation (DIC) (diagnosis)", "Disseminated intravascular coagulation [defibrination syndrome]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disseminated intravascular coagulation", "shortest_name_length": 3}
{"curie": "MONDO:0013790", "names": ["MRMV2", "MIRROR MOVEMENTS 2", "mirror movements 2", "mirror movements type 2", "RAD51 familial congenital mirror movements", "familial congenital mirror movements caused by mutation in RAD51"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mirror movements 2", "shortest_name_length": 5}
{"curie": "MONDO:0002410", "names": ["Pyelitis cystica", "pyelitis cystica", "pyelitis; cystica", "cystica; pyelitis", "ureteritis cystica", "Ureteritis Cystica", "Ureteritis cystica", "cystica; ureteritis", "ureteritis; cystica", "Pyeloureteritis cystica", "pyeloureteritis cystica", "pyelitis cystica (diagnosis)", "ureteritis cystica (diagnosis)", "Pyeloureteritis cystica (disorder)", "pyeloureteritis cystica (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyeloureteritis cystica", "shortest_name_length": 16}
{"curie": "MONDO:0017800", "names": ["pseudo-Meigs syndrome", "pseudo-Demons-Meigs syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudo-Meigs syndrome", "shortest_name_length": 21}
{"curie": "UMLS:C4525892", "names": ["Stage I Pancreatic Neuroendocrine Tumor", "Stage I Pancreatic Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Pancreatic Neuroendocrine Tumor AJCC v8", "shortest_name_length": 39}
{"curie": "MONDO:0002429", "names": ["IIP", "IIp", "IPF", "noninfectious pneumonia", "Idiopathic fibrosing alveolitis", "idiopathic fibrosing alveolitis", "idiopathic interstitial pneumonia", "Idiopathic Interstitial Pneumonia", "Idiopathic interstitial pneumonia", "interstitial pneumonia idiopathic", "Pneumonia, Idiopathic Interstitial", "Idiopathic Interstitial Pneumonias", "Interstitial Pneumonia, Idiopathic", "Idiopathic Interstitial Pneumonitis", "Pneumonias, Idiopathic Interstitial", "Interstitial Pneumonias, Idiopathic", "idiopathic interstitial pneumonitis", "diffuse idiopathic pulmonary fibrosis", "Diffuse idiopathic pulmonary fibrosis", "Idiopathic interstitial pneumonia (disorder)", "Idiopathic interstitial pneumonia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic interstitial pneumonia", "shortest_name_length": 3}
{"curie": "MONDO:0002385", "names": ["Cystic nephroma", "Cystic Nephroma", "cystic nephroma", "Adult Cystic Nephroma", "adult cystic nephroma", "benign cystic nephroma", "Benign cystic nephroma", "Benign Cystic Nephroma", "benign multilocular cystic nephroma", "Benign cystic nephroma (morphologic abnormality)", "multilocular cystic nephroma, mixed epithelial stromal tumour and renal epithelial stromal tumour"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign cystic nephroma", "shortest_name_length": 15}
{"curie": "MONDO:0013000", "names": ["Doss porphyria", "Doss Porphyria", "ALAD porphyria", "DOSS PORPHYRIA", "ALAD DEFICIENCY", "ALAD Deficiency", "ALAD deficiency", "PORPHYRIA, ALAD", "porphyria, ALAD", "ALADH deficiency", "porphyria of Doss", "Porphyria of Doss", "Acute hepatic porphyria", "acute hepatic porphyria", "Acute Hepatic Porphyria", "Porphyria, Acute Hepatic", "porphyria, acute hepatic", "PORPHYRIA, ACUTE HEPATIC", "porphyria due to ALAD deficiency", "Porphyria due to ALAD deficiency", "LEAD POISONING, SUSCEPTIBILITY TO", "Lead poisoning, susceptibility to", "porphobilinogen synthase deficiency", "Porphobilinogen Synthase Deficiency", "ALA dehydratase deficiency pophyria", "PORPHOBILINOGEN SYNTHASE DEFICIENCY", "Porphobilinogen synthase deficiency", "ALA dehydratase deficiency porphyria", "Hereditary delta-aminolevulinic aciduria", "delta-Aminolevulinate dehydrase deficiency", "Delta-aminolevulinate dehydrase deficiency", "Delta-aminolaevulinate dehydrase deficiency", "Porphyria due to ALA dehydratase deficiency", "delta-Aminolaevulinate dehydrase deficiency", "porphyria due to ALA dehydratase deficiency", "Delta-aminolevulinate dehydratase deficiency", "DELTA-AMINOLEVULINATE DEHYDRATASE DEFICIENCY", "Delta-Aminolevulinate Dehydratase Deficiency", "Porphobilinogen synthase deficiency (disorder)", "aminolevulinate dehydratase deficiency porphyria", "delta-Aminolevulinic acid dehydratase deficiency", "delta-Aminolaevulinic acid dehydratase deficiency", "5-aminolevulinic acid dehydratase deficiency porphyria", "ALA - Aminolevulinic acid dehydratase deficiency porphyria", "ALA - Aminolaevulinic acid dehydratase deficiency porphyria", "Porphyria due to delta-aminolevulinate dehydratase deficiency", "porphyria due to delta-aminolevulinate dehydratase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "porphyria due to ALA dehydratase deficiency", "shortest_name_length": 14}
{"curie": "UMLS:C3495931", "names": ["Vestibular toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vestibular toxicity", "shortest_name_length": 19}
{"curie": "MONDO:0012636", "names": ["RLS6", "restless legs syndrome 6", "periodic limb movements in sleep", "PERIODIC LIMB MOVEMENTS IN SLEEP", "restless legs syndrome, susceptibility to, 6", "RESTLESS LEGS SYNDROME, SUSCEPTIBILITY TO, 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "restless legs syndrome, susceptibility to, 6", "shortest_name_length": 4}
{"curie": "MONDO:0022096", "names": ["angiogranuloma", "angiogranulomas", "Lobular Hemangioma", "PYOGENIC GRANULOMA", "granuloma pyogenic", "lobular hemangioma", "GRANULOMA PYOGENIC", "Pyogenic granuloma", "Pyogenic Granuloma", "pyogenic granuloma", "granulomas pyogenic", "granuloma; pyogenic", "pyogenic; granuloma", "Granuloma, Pyogenic", "Granulomatous polyp", "granuloma pyogenicum", "Granuloma Pyogenicum", "Granuloma pyogenicum", "Granuloma, suppurative", "granulomata pyogenicum", "Granulomata Pyogenicum", "PG - Pyogenic granuloma", "Granuloma Telangiecticum", "granuloma telangiecticum", "adult lobular hemangioma", "pyogenic granuloma of skin", "Granuloma telangiectaticum", "Pyogenic granuloma of skin", "granuloma; telangiectaticum", "Granuloma, telangiectaticum", "telangiectaticum; granuloma", "Lobular capillary hemangioma", "capillary lobular hemangioma", "lobular capillary hemangioma", "Lobular Capillary Hemangioma", "Lobular capillary haemangioma", "hemangioma, Lobular Capillary", "Suppurative granuloma of skin", "Capillary Hemangioma, Lobular", "Hemangioma, Lobular Capillary", "Pyogenic granuloma (disorder)", "pyogenic granuloma (diagnosis)", "Hemangiomatous granulation tissue", "hemangiomatous Granulation Tissue", "hemangiomatous granulation tissue", "Hemangiomatous Granulation Tissue", "Granulation Tissue-Type Hemangioma", "Granuloma telangiectaticum of skin", "granulation tissue-type hemangioma", "Pyogenic granuloma of skin (disorder)", "pyogenic granuloma of skin (diagnosis)", "Granuloma pyogenicum (morphologic abnormality)", "Capillary hemangioma of granulation tissue type", "Capillary haemangioma of granulation tissue type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyogenic granuloma", "shortest_name_length": 14}
{"curie": "MONDO:0012072", "names": ["FPLD1", "familial partial lipodystrophy type 1", "Familial partial lipodystrophy type 1", "Familial Partial Lipodystrophy, Type 1", "Lipodystrophy, Familial Partial, Type 1", "lipodystrophy, familial partial, type 1", "LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 1", "familial partial lipodystrophy type Köbberling", "Familial partial lipodystrophy Kobberling type", "familial partial lipodystrophy Kobberling type", "Familial Partial Lipodystrophy, Kobberling Type", "Familial partial lipodystrophy, Köbberling type", "familial partial lipodystrophy, Kobberling type", "familial partial lipodystrophy, Köbberling type", "Lipodystrophy, Familial Partial, Kobberling Type", "LIPODYSTROPHY, FAMILIAL PARTIAL, KOBBERLING TYPE", "lipodystrophy, familial partial, Kobberling type", "Familial partial lipodystrophy Kobberling type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial partial lipodystrophy, Kobberling type", "shortest_name_length": 5}
{"curie": "MONDO:0013375", "names": ["KFS3", "Klippel-Feil syndrome 3", "GDF3 isolated Klippel-Feil syndrome", "Klippel-Feil syndrome 3, autosomal dominant", "KLIPPEL-FEIL SYNDROME 3, AUTOSOMAL DOMINANT", "Klippel-FEIL syndrome 3, autosomal dominant", "isolated Klippel-Feil syndrome caused by mutation in GDF3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Klippel-Feil syndrome 3, autosomal dominant", "shortest_name_length": 4}
{"curie": "UMLS:C1261282", "names": ["complications liver transplant", "complications; liver transplant", "Transplanted Liver Complication", "liver transplant; complications", "Complications of liver transplant", "complications of liver transplant", "Complication of Transplanted Liver", "Complication of transplanted liver", "complication of transplanted liver", "Complications of transplanted liver", "Complication of transplanted liver (disorder)", "complications of liver transplant (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Complication of transplanted liver", "shortest_name_length": 30}
{"curie": "UMLS:C1333858", "names": ["Grade 3 Rectal Adenocarcinoma", "Grade III Rectal Adenocarcinoma", "Poorly Differentiated Rectal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade 3 Rectal Adenocarcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0017043", "names": ["CMN", "CMn", "Mesoblastic nephroma", "mesoblastic nephroma", "Mesoblastic Nephroma", "STROMAL NEPHROMA, MALIGNANT", "stromal nephroma, malignant", "Congenital mesoblastic nephroma", "congenital mesoblastic nephroma", "Congenital Mesoblastic Nephroma", "Congenital Mesoblastic Nephromas", "Nephroma, Congenital Mesoblastic", "Mesoblastic Nephroma, Congenital", "Mesoblastic Nephromas, Congenital", "Nephromas, Congenital Mesoblastic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital mesoblastic nephroma", "shortest_name_length": 3}
{"curie": "MONDO:0000414", "names": ["pediatric electroclinical syndrome", "childhood electroclinical syndrome", "electroclinical syndrome of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood electroclinical syndrome", "shortest_name_length": 34}
{"curie": "MONDO:0000630", "names": ["immune organ benign neoplasm", "immune system organ benign neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immune system organ benign neoplasm", "shortest_name_length": 28}
{"curie": "UMLS:C5206376", "names": ["Refractory Rectal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Rectal Carcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0014318", "names": ["HPMRS4", "HPMRS6", "GPIBD10", "GPIBD62", "GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 10", "glycosylphosphatidylinositol biosynthesis defect 62", "glycosylphosphatidylinositol biosynthesis defect 10", "hyperphosphatasia with mental retardation syndrome 6", "hyperphosphatasia with mental retardation syndrome 4", "HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 4", "PGAP3 hyperphosphatasia-intellectual disability syndrome", "hyperphosphatasia with mental retardation syndrome type 4", "hyperphosphatasia with intellectual disability syndrome 4", "hyperphosphatasia with intellectual disability syndrome type 4", "HYPERPHOSPHATASIA WITH IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME 4", "hyperphosphatasia with impaired intellectual development syndrome 4", "hyperphosphatasia-intellectual disability syndrome caused by mutation in PGAP3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperphosphatasia with intellectual disability syndrome 4", "shortest_name_length": 6}
{"curie": "UMLS:C4682892", "names": ["Ureter Cancer by AJCC v8 Stage", "Ureter Urothelial Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ureter Cancer by AJCC v8 Stage", "shortest_name_length": 30}
{"curie": "UMLS:C0855188", "names": ["Stage I Bladder Squamous Cell Cancer", "Bladder squamous cell carcinoma stage I", "Squamous cell bladder carcinoma stage I", "Bladder Squamous Cell Carcinoma Stage I", "Stage I Squamous Cell Carcinoma of Bladder", "Squamous cell carcinoma of the bladder stage I", "Stage I Squamous Cell Carcinoma of the Bladder", "Stage I Squamous Cell Carcinoma of the Bladder AJCC v7", "Stage I Squamous Cell Carcinoma of the Bladder AJCC v6", "Stage I Squamous Cell Carcinoma of the Bladder AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder squamous cell carcinoma stage I", "shortest_name_length": 36}
{"curie": "UMLS:C0862206", "names": ["Mycosis fungoides/Sezary syndrome refractory", "Refractory Mycosis Fungoides and Sezary Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mycosis fungoides/Sezary syndrome refractory", "shortest_name_length": 44}
{"curie": "MONDO:0002325", "names": ["erosion teeth", "erosion tooth", "Tooth erosion", "teeth erosion", "TOOTH EROSION", "tooth erosion", "Tooth Erosion", "Dental Erosion", "Teeth--Erosion", "Tooth Erosions", "dental erosion", "Erosion, Tooth", "erosion dental", "Erosion, Dental", "erosion; dental", "dental; erosion", "Dental Erosions", "Erosion of teeth", "erosion of teeth", "localized erosion", "generalized erosion", "Erosion of teeth NOS", "Erosion of teeth, NOS", "Erosion of teeth (disorder)", "tooth erosion, non-bacterial", "erosion of teeth (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tooth erosion, non-bacterial", "shortest_name_length": 13}
{"curie": "UMLS:C5554912", "names": ["Locally Advanced Digestive System Neuroendocrine Neoplasm", "Locally Advanced Gastroenteropancreatic Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Digestive System Neuroendocrine Neoplasm", "shortest_name_length": 57}
{"curie": "MONDO:0019419", "names": ["Johnson syndrome", "X-linked intellectual disability-macrocephaly-macroorchidism syndrome", "x-linked intellectual disability, macrocephaly, macroorchidism syndrome", "X-linked intellectual disability, macrocephaly, macroorchidism syndrome", "X-linked intellectual disability, macrocephaly, macroorchidism syndrome (disorder)", "x-linked intellectual disability, macrocephaly, macroorchidism syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability-macrocephaly-macroorchidism syndrome", "shortest_name_length": 16}
{"curie": "UMLS:C0393835", "names": ["Diabetic asymmetric polyneuropathy", "Diabetic Asymmetric Polyneuropathy", "Polyneuropathy, Diabetic Asymmetric", "Asymmetric Polyneuropathy, Diabetic", "Diabetic Asymmetric Polyneuropathies", "Asymmetric Polyneuropathies, Diabetic", "Polyneuropathies, Diabetic Asymmetric", "Asymmetric polyneuropathy due to diabetes mellitus", "Asymmetric polyneuropathy due to diabetes mellitus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diabetic Asymmetric Polyneuropathy", "shortest_name_length": 34}
{"curie": "UMLS:C0751741", "names": ["Putamen bleeding", "putamen hemorrhage", "Putamen hemorrhage", "Putamen Hemorrhage", "Putamen haemorrhage", "Hemorrhage, Putamen", "putaminal hemorrhage", "Putaminal Hemorrhage", "Hemorrhage in putamen", "Hemorrhage, Putaminal", "Haemorrhage in putamen", "Brain Hemorrhage, Putaminal", "Brain Hemorrhages, Putaminal", "Hemorrhage in putamen (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Putaminal Hemorrhage", "shortest_name_length": 16}
{"curie": "MONDO:0043726", "names": ["mof", "mods", "MODS", "MOF syndrome", "multiorgan failure", "MULTIORGAN FAILURE", "Multiorgan failure", "Multi-organ failure", "failure multi-organ", "multi-organ failure", "Multi-Organ Failure", "failure multi organ", "multi organ failure", "Multi organ failure", "failure multiple organ", "multiple organ failure", "MULTIPLE ORGAN FAILURE", "Multiple organ failure", "Multiple Organ Failure", "multiple organ failures", "Multiple Organ Failures", "organ failure, multiple", "failure, multiple organ", "Multiple System Failure", "Failure, Multiple Organ", "Organ Failure, Multiple", "multisystem organ failure", "Multisystem organ failure", "Multiple organ failure, NOS", "MOF - Multiple organ failure", "multiple organ system failure", "multiple system organ failure", "multiple organ systems failure", "multiple systems organ failure", "Multiple systems organ failure", "Multiple organ systems failure", "Multiple organ failure (disorder)", "multiple organ failure (diagnosis)", "Multiple organ dysfunction syndrome", "Multiple Organ Dysfunction Syndrome", "multiple organ dysfunction syndrome", "Organ Dysfunction Syndrome, Multiple", "organ dysfunction syndrome, multiple", "MOSF - Multiple organ systems failure", "MSOF - Multiple systems organ failure", "MODS - Multiple organ dysfunction syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple organ dysfunction syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0009351", "names": ["Homocarnosinosis", "HOMOCARNOSINOSIS", "homocarnosinosis", "homocarnosinase deficiency", "HOMOCARNOSINASE DEFICIENCY", "Homocarnosinase deficiency", "Serum carnosinase deficiency", "Homocarnosinase deficiency (disorder)", "homocarnosinase deficiency (diagnosis)", "disorders of peptide metabolism homocarnosinase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "homocarnosinosis", "shortest_name_length": 16}
{"curie": "UMLS:C5419742", "names": ["Locally Advanced Kidney Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Kidney Carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0002057", "names": ["breast leiomyoma", "Breast Leiomyoma", "leiomyoma of breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast leiomyoma", "shortest_name_length": 16}
{"curie": "UMLS:C4329683", "names": ["Congenital Ovarian Failure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Ovarian Failure", "shortest_name_length": 26}
{"curie": "MONDO:0015800", "names": ["osteosclerosis-developmental delay-craniosynostosis syndrome", "Osteosclerosis-developmental delay-craniosynostosis syndrome", "Osteosclerosis, developmental delay, craniosynostosis syndrome", "Osteosclerosis, developmental delay, craniosynostosis syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteosclerosis-developmental delay-craniosynostosis syndrome", "shortest_name_length": 60}
{"curie": "MONDO:0020023", "names": ["respiratory or mediastinal malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "respiratory or mediastinal malformation", "shortest_name_length": 39}
{"curie": "MONDO:0008283", "names": ["intestinal polyposi", "Intestinal polyposis", "Intestinal Polyposis", "intestinal polyposis", "Polyposis intestinal", "polyposis intestinal", "intestinal; polyposis", "polyposis; intestinal", "Polyposis, Intestinal", "Cronkhite-Canada disease", "Canada-Cronkhite syndrome", "Cronkhite-Canada syndrome", "cronkhite-canada syndrome", "CRONKHITE-CANADA SYNDROME", "Cronkhite-Canada Syndrome", "Cronkhite-Canada polyposis", "Multiple intestinal polyps", "CCS - Cronkhite-Canada syndrome", "Gastric Cronkhite Canada Polyposis", "gastric Cronkhite Canada polyposis", "Cronkhite-Canada syndrome (disorder)", "cronkhite-canada syndrome (diagnosis)", "Gastrointestinal multiple polyposis syndrome", "gastrointestinal polyposis-ectodermal changes syndrome", "Gastrointestinal polyposis-ectodermal changes syndrome", "polyposis skin pigmentation alopecia fingernail changes", "POLYPOSIS, SKIN PIGMENTATION, ALOPECIA, AND FINGERNAIL CHANGES", "polyposis, skin pigmentation, alopecia, and fingernail changes", "Polyposis, Skin Pigmentation, Alopecia, And Fingernail Changes", "gastrointestinal polyposis-skin pigmentation-alopecia-fingernail changes syndrome", "Gastrointestinal polyposis-skin pigmentation-alopecia-fingernail changes syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cronkhite-Canada syndrome", "shortest_name_length": 19}
{"curie": "MONDO:0008634", "names": ["urticaria, familial localized heat", "Urticaria, Familial Localized Heat", "URTICARIA, FAMILIAL LOCALIZED HEAT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urticaria, familial localized heat", "shortest_name_length": 34}
{"curie": "UMLS:C5669680", "names": ["Lung Plasmacytoma", "Plasmacytoma of Lung", "Primary Lung Plasmacytoma", "Primary Extraosseous Lung Plasmacytoma", "Primary Extramedullary Lung Plasmacytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Plasmacytoma", "shortest_name_length": 17}
{"curie": "UMLS:C0280346", "names": ["Stage I Mouth Mucoepidermoid Carcinoma", "Stage I Oral Cavity Mucoepidermoid Cancer", "Stage I Mucoepidermoid Carcinoma of Mouth", "Stage I Oral Cavity Mucoepidermoid Carcinoma", "oral cavity mucoepidermoid carcinoma, stage I", "Stage I Mucoepidermoid Carcinoma of the Mouth", "Stage I Mucoepidermoid Carcinoma of Oral Cavity", "Mucoepidermoid carcinoma of the oral cavity stage I", "stage I mucoepidermoid carcinoma of the oral cavity", "Stage I Mucoepidermoid Carcinoma of the Oral Cavity", "mucoepidermoid carcinoma of the oral cavity, stage I", "Stage I Oral Cavity Mucoepidermoid Carcinoma AJCC v6", "Stage I Oral Cavity Mucoepidermoid Carcinoma AJCC v7", "Stage I Oral Cavity Mucoepidermoid Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mucoepidermoid carcinoma of the oral cavity stage I", "shortest_name_length": 38}
{"curie": "UMLS:C0730512", "names": ["BLINDNESS FUNCTIONAL", "functional visual loss", "Functional visual loss", "Nonphysiologic vision loss", "Nonphysiologic acuity loss", "Functional visual loss (disorder)", "functional visual loss (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Functional visual loss", "shortest_name_length": 20}
{"curie": "UMLS:C3839736", "names": ["Sensitization", "Sensitisation", "Sensitization (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sensitization (disorder)", "shortest_name_length": 13}
{"curie": "UMLS:C0744254", "names": ["Gallbladder Infection", "GALLBLADDER INFECTION", "Gallbladder infection", "infection gallbladder", "gallbladder infection", "gallbladder infections", "gallbladder; infection", "infection; gallbladder", "gallbladder infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gallbladder Infection", "shortest_name_length": 21}
{"curie": "MONDO:0100432", "names": ["FNIP1 deficiency", "FNIP1-associated syndrome", "immunodeficiency with cardiomyopathy and pre-excitation syndrome", "absent B cells, agammaglobulinemia, and hypertrophic cardiomyopathy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FNIP1-associated syndrome", "shortest_name_length": 16}
{"curie": "UMLS:C0855086", "names": ["Refractory Nodular Sclerosis Hodgkin Lymphoma", "Hodgkin's disease nodular sclerosis refractory", "Refractory Nodular Sclerosis Hodgkin's Disease", "Refractory Nodular Sclerosis Hodgkin's Lymphoma", "Refractory Nodular Sclerosis Classic Hodgkin Lymphoma", "Refractory Nodular Sclerosis Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's disease nodular sclerosis refractory", "shortest_name_length": 45}
{"curie": "DOID:3660", "names": ["allergy wheat", "wheat allergy", "Wheat Allergy", "Allergy, Wheat", "Wheat Allergies", "allergies wheat", "wheat allergies", "allergy to wheat", "Allergy to wheat", "Allergies, Wheat", "Wheat Hypersensitivity", "wheat hypersensitivity", "wheat allergic reaction", "Hypersensitivity, Wheat", "Wheat Hypersensitivities", "Hypersensitivities, Wheat", "Allergy to wheat (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "wheat allergy", "shortest_name_length": 13}
{"curie": "MONDO:0021025", "names": ["cirrhosis, familial", "cirrhosis, familial, with antigenemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cirrhosis, familial, with antigenemia", "shortest_name_length": 19}
{"curie": "UMLS:C4727375", "names": ["Recurrent Invasive Ductal Breast Carcinoma", "Recurrent Invasive Breast Ductal Carcinoma", "Recurrent Invasive Ductal Carcinoma of the Breast", "Recurrent Invasive Breast Carcinoma of No Special Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Invasive Breast Carcinoma of No Special Type", "shortest_name_length": 42}
{"curie": "MONDO:0035133", "names": ["DIDOD", "CHUJANS", "CHUNG-JANSEN SYNDROME", "Chung-Jansen syndrome", "Chung Jansen syndrome", "DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHISM", "developmental delay, intellectual disability, obesity, and dysmorphic features", "PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome", "PHIP-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome", "PHIP-related behavioural problems, intellectual disability, obesity, dysmorphic features syndrome", "Pleckstrin homology domain interacting protein-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome", "Pleckstrin homology domain interacting protein-related behavioural problems, intellectual disability, obesity, dysmorphic features syndrome", "Pleckstrin homology domain interacting protein-related behavioral problems, intellectual disability, obesity, dysmorphic features syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C4524714", "names": ["Clinical Stage IIA Gastroesophageal Junction Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage IIA Gastroesophageal Junction Adenocarcinoma AJCC v8", "shortest_name_length": 67}
{"curie": "MONDO:0043310", "names": ["Amaurosis fugax", "amaurosis fugax", "AMAUROSIS FUGAX", "Amaurosis Fugax", "amaurosis; fugax", "fugax; amaurosis", "Momentary blindness", "momentary blindness", "Amaurosis temporary", "AF - Amaurosis fugax", "AFx - Amaurosis fugax", "Amaurosis fugax (disorder)", "amaurosis fugax (diagnosis)", "Momentary blindness syndrome", "Transient monocular blindness", "Transient Monocular Blindness", "transient monocular blindness", "TRANSIENT MONOCULAR BLINDNESS", "monocular blindness, transient", "blindness, transient monocular", "Blindness, Transient Monocular", "Monocular Blindness, Transient", "Blindness, Monocular, Transient", "blindness, monocular, transient", "Temporary blindness due to vascular insufficiency", "Amaurosis fugax (one sided temporary vision loss)", "amaurosis fugax (one sided temporary vision loss)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amaurosis fugax", "shortest_name_length": 15}
{"curie": "MONDO:0022777", "names": ["cleft lip palate dysmorphism kumar type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleft lip palate dysmorphism kumar type", "shortest_name_length": 39}
{"curie": "MONDO:0032815", "names": ["MTDPS17", "MITOCHONDRIAL DNA DEPLETION SYNDROME 17", "mitochondrial DNA depletion syndrome 17"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial DNA depletion syndrome 17", "shortest_name_length": 7}
{"curie": "MONDO:0014448", "names": ["FDH", "FDAH", "bisalbuminemia", "euthyroid hyperthyroxinemia 1", "EUTHYROID HYPERTHYROXINEMIA 1", "dysalbuminemic hyperthyroxinemia", "Familial Dysalbuminemic Hyperthyroidism", "dysalbuminemic hypertriiodothyroninemia", "familial Dysalbuminemic hyperthyroidism", "familial Dysalbuminemic hyperthyroxinemia", "Familial Dysalbuminemic Hyperthyroxinemia", "Familial dysalbuminemic hyperthyroxinemia", "Familial dysalbuminaemic hyperthyroxinemia", "HYPERTHYROXINEMIA, FAMILIAL DYSALBUMINEMIC", "Hyperthyroxinemia, Familial Dysalbuminemic", "Dysalbuminemic Hyperthyroxinemia, Familial", "hyperthyroxinemia, familial dysalbuminemic", "hyperthyroxinemia, familial Dysalbuminemic", "Familial dysalbuminaemic hyperthyroxinaemia", "HYPERTRIIODOTHYRONINEMIA, FAMILIAL DYSALBUMINEMIC", "Familial dysalbuminemic hyperthyroxinemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperthyroxinemia, familial dysalbuminemic", "shortest_name_length": 3}
{"curie": "UMLS:C0457190", "names": ["Xanthomatous meningioma", "Xanthomatous Meningioma", "Xanthomatous Meningiomas", "Meningioma, Xanthomatous", "Meningiomas, Xanthomatous", "Xanthomatous meningioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Xanthomatous Meningioma", "shortest_name_length": 23}
{"curie": "EFO:1001282", "names": ["Candidemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Candidemia", "shortest_name_length": 10}
{"curie": "UMLS:C3495950", "names": ["Cochlear toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cochlear toxicity", "shortest_name_length": 17}
{"curie": "MONDO:0010819", "names": ["STGD3", "Stargardt disease-3", "Stargardt disease 3", "STARGARDT DISEASE 3", "Stargardt disease type 3", "Stargardt disease-3 (diagnosis)", "MACULAR DYSTROPHY WITH FLECKS, TYPE 3", "Macular dystrophy with flecks, type 3", "macular dystrophy with flecks, type 3", "STARGARDT-LIKE MACULAR DYSTROPHY, AUTOSOMAL DOMINANT", "Stargardt-like macular dystrophy, autosomal dominant", "Stargardt-Like Macular Dystrophy, Autosomal Dominant", "Macular dystrophy, autosomal dominant, chromosome 6-linked,"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stargardt disease 3", "shortest_name_length": 5}
{"curie": "UMLS:C2986683", "names": ["Stage I AIDS-Related Lymphoma", "stage I AIDS-related lymphoma", "Ann Arbor Stage I AIDS-Related Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage I AIDS-Related Lymphoma", "shortest_name_length": 29}
{"curie": "MONDO:0006013", "names": ["visna", "Visna", "Visnas", "visna disease", "Ovine Encephalomyelitis", "Encephalomyelitis, Ovine", "Ovine Encephalomyelitides", "Encephalomyelitides, Ovine", "Visna/maedi virus infectious disease", "Visna/maedi virus disease or disorder", "Visna/maedi virus caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "visna disease", "shortest_name_length": 5}
{"curie": "MONDO:0043264", "names": ["impact seizure", "impact seizures", "Traumatic epilepsy", "traumatic epilepsy", "Traumatic Epilepsy", "Epilepsy, Traumatic", "epilepsy; traumatic", "epilepsy, traumatic", "traumatic; epileptic", "Traumatic Epilepsies", "traumatic Epilepsies", "concussive convulsion", "Epilepsies, Traumatic", "Epilepsies, traumatic", "concussive convulsions", "convulsion, concussive", "EPILEPSY POSTTRAUMATIC", "posttraumatic epilepsy", "Post-Traumatic Epilepsy", "Post-traumatic epilepsy", "epilepsy post-traumatic", "post-traumatic epilepsy", "post traumatic epilepsy", "convulsions, concussive", "Epilepsy, Post-Traumatic", "Epilepsy, Post Traumatic", "epilepsy, post traumatic", "Post-Traumatic Epilepsies", "epilepsy following trauma", "post-traumatic Epilepsies", "Epilepsies, Post-Traumatic", "Epilepsies, post-traumatic", "Late Post-Traumatic Seizure", "late post-traumatic seizure", "post-traumatic seizure, late", "Post-Traumatic Seizure, Late", "Late Post Traumatic Seizures", "early post-traumatic seizure", "late post traumatic seizures", "seizure, late post-traumatic", "Late Post-Traumatic Seizures", "Seizure, Late Post-Traumatic", "late post-traumatic seizures", "seizures, late post-traumatic", "Seizures, Late Post-Traumatic", "post-traumatic seizures, late", "PTE - Post-traumatic epilepsy", "early post-traumatic seizures", "post-traumatic seizure, early", "Post-Traumatic Seizures, Late", "PTE - post-traumatic epilepsy", "seizure, early post-traumatic", "early post traumatic seizures", "seizures, early post-traumatic", "post-traumatic seizures, early", "Post-traumatic seizure disorder", "Post Traumatic Seizure Disorder", "post-traumatic seizure disorder", "post traumatic seizure disorder", "Post-Traumatic Seizure Disorder", "Post-Traumatic Seizure Disorders", "seizure disorder, post-traumatic", "post-traumatic seizure disorders", "Disorder, Post-Traumatic Seizure", "Seizure Disorder, Post-Traumatic", "disorder, post-traumatic seizure", "Seizure Disorder, Post Traumatic", "seizure disorder, post traumatic", "Seizure Disorders, Post-Traumatic", "disorders, post-traumatic seizure", "seizure disorders, post-traumatic", "Disorders, Post-Traumatic Seizure", "Post-traumatic epilepsy (disorder)", "Post-traumatic epilepsy (diagnosis)", "Epilepsy due to and following traumatic brain injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "post-traumatic epilepsy", "shortest_name_length": 14}
{"curie": "MONDO:0000757", "names": ["steroid-induced osteoporosis", "glucocorticoid-induced osteoporosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glucocorticoid-induced osteoporosis", "shortest_name_length": 28}
{"curie": "MONDO:0016824", "names": ["IMS", "myofibromatosis", "Myofibromatoses", "Myofibromatosis", "lipofibromatosis", "infantile myofibromatosis", "Infantile Myofibromatosis", "Infantile myofibromatosis", "Multicentric Myofibromatosis", "Infantile Hemangiopericytoma", "infantile hemangiopericytoma", "multicentric myofibromatosis", "Myofibromatosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile myofibromatosis", "shortest_name_length": 3}
{"curie": "MONDO:0010578", "names": ["MTS", "DDP", "DDS", "DDON syndrome", "Jensen syndrome", "JENSEN SYNDROME", "Mohr-Tranebjærg Syndrome", "Mohr-Tranebjaerg syndrome", "MOHR-TRANEBJAERG SYNDROME", "MOHR-Tranebjaerg syndrome", "Deafness-Dystonia Syndrome", "Dystonia-Deafness Syndrome", "dystonia-deafness syndrome", "Deafness-dystonia syndrome", "Deafness dystonia syndrome", "dystonia deafness syndrome", "deafness dystonia syndrome", "DYSTONIA-DEAFNESS SYNDROME", "Dystonia Deafness Syndrome", "Mohr-Tranebjaerg syndrome (MTS)", "X-linked recessive deafness syndrome", "deafness-Dystonia-optic atrophy syndrome", "DEAFNESS-DYSTONIA-OPTIC ATROPHY SYNDROME", "deafness dystonia optic atrophy syndrome", "Deafness Dystonia Optic Atrophy Syndrome", "Deafness-dystonia-optic atrophy syndrome", "Opticoacustic nerve atrophy with dementia", "OPTICOACOUSTIC NERVE ATROPHY WITH DEMENTIA", "Opticoacoustic Nerve Atrophy With Dementia", "deafness-dystonia-optic neuronopathy syndrome", "Deafness Dystonia Optic Neuronopathy Syndrome", "Deafness-Dystonia-Optic Neuronopathy Syndrome", "Deafness-dystonia-optic neuronopathy syndrome", "Mohr-Tranebjaerg syndrome, X-linked recessive", "deafness dystonia optic neuronopathy syndrome", "Nerve deafness optic nerve atrophy, and dementia", "Hearing loss-dystonia-optic neuronopathy syndrome", "deafness - dystonia - optic neuronopathy syndrome", "deafness-dystonia-optic neuronopathy (DDON) syndrome", "deafness dystonia optic neuronopathy syndrome (DDON)", "Syndrome of opticoacoustic nerve atrophy with dementia", "Deafness-dystonia-optic neuronopathy syndrome (disorder)", "Deafness (DFN-1) dystonia, mental deficiency and blindness", "deafness syndrome, progressive, with blindness, dystonia, fractures, and mental deficiency", "Deafness Syndrome, Progressive, With Blindness, Dystonia, Fractures, And Mental Deficiency", "DEAFNESS SYNDROME, PROGRESSIVE, WITH BLINDNESS, DYSTONIA, FRACTURES, AND MENTAL DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness dystonia syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0001255", "names": ["Humidifier lung", "humidifier lung", "humidifiers lung", "Sauna takers lung", "air conditioner lung", "Air conditioner lung", "air-conditioner; lung", "ventilation pneumonitis", "Ventilation pneumonitis", "pneumonitis; ventilation", "ventilation systems lung", "ventilation; pneumonitis", "\"Ventilation\" pneumonitis", "air humidifier pneumonitis", "Humidifier lung (disorder)", "air-conditioner; pneumonitis", "pneumonitis; air-conditioner", "'air conditioning' pneumonitis", "air-conditioner humidifier lung", "air humidifier lung or pneumonitis", "Air conditioner and humidifier lung", "Air-conditioner and humidifier lung", "Humidifier and air-conditioner pneumonitis", "Humidifier and air conditioning pneumonitis", "Humidifier AND/OR air conditioning pneumonitis", "Air conditioner and humidifier lung (diagnosis)", "hypersensitivity pneumonitis due to air conditioning", "hypersensitivity pneumonitis due to air conditioning (diagnosis)", "hypersensitivity pneumonitis - air conditioner and humidifier lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ventilation pneumonitis", "shortest_name_length": 15}
{"curie": "MONDO:0012193", "names": ["LGMDD3", "LGMD1G", "LGMD type 1G", "HNRNPDL-related LGMD D3", "Limb-girdle muscular dystrophy type 1G", "muscular dystrophy limb-girdle type 1G", "limb-girdle muscular dystrophy type 1G", "Limb-Girdle Muscular Dystrophy, Type 1G", "limb-girdle muscular dystrophy, type 1G", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1G", "HNRNPDL-related limb-girdle muscular dystrophy D3", "LIMB-GIRDLE MUSCULAR DYSTROPHY, TYPE 1G (disorder)", "muscular dystrophy, limb-girdle, autosomal dominant 3", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 3", "autosomal dominant limb-girdle muscular dystrophy type 3", "Autosomal dominant limb-girdle muscular dystrophy type 1G", "autosomal dominant limb-girdle muscular dystrophy type 1G", "HNRNPDL autosomal dominant limb-girdle muscular dystrophy", "Autosomal dominant limb girdle muscular dystrophy type 1G", "Autosomal dominant limb girdle muscular dystrophy type 1G (disorder)", "autosomal dominant limb-girdle muscular dystrophy caused by mutation in HNRNPDL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant limb-girdle muscular dystrophy type 1G", "shortest_name_length": 6}
{"curie": "UMLS:C0854779", "names": ["Relapsed Rectosigmoid Cancer", "Rectosigmoid cancer recurrent", "Recurrent Rectosigmoid Cancer", "Rectosigmoid Cancer, Recurrent", "Recurrent Rectosigmoid Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rectosigmoid cancer recurrent", "shortest_name_length": 28}
{"curie": "MONDO:0012582", "names": ["SMDP3", "Surfactant Metabolism Dysfunction-3", "Surfactant Protein ABCA3 Deficiency", "Surfactant Apoprotein ABCA3 Deficiency", "Pulmonary Alveolar Proteinosis, Congenital, 3", "Pulmonary Surfactant Metabolism Dysfunction-3", "PULMONARY ALVEOLAR PROTEINOSIS, CONGENITAL, 3", "pulmonary alveolar proteinosis, congenital, 3", "surfactant metabolism dysfunction, pulmonary, 3", "Surfactant Metabolism Dysfunction, Pulmonary, 3", "SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 3", "Interstitial Lung Disease Due To ABCA3 Deficiency", "interstitial lung disease due to ABCA3 deficiency", "INTERSTITIAL LUNG DISEASE DUE TO ABCA3 DEFICIENCY", "Interstitial lung disease due to ABCA3 deficiency", "surfactant metabolism dysfunction, pulmonary, type 3", "interstitial lung disease due to ATP-binding cassette subfamily A member 3 deficiency", "Interstitial lung disease due to ATP-binding cassette subfamily A member 3 deficiency", "Interstitial lung disease due to ABCA3 (ATP-binding cassette subfamily A member 3) deficiency", "Interstitial lung disease due to ATP-binding cassette subfamily A member 3 deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "interstitial lung disease due to ABCA3 deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0016977", "names": ["moderately-differentiated thymic neuroendocrine carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "moderately-differentiated thymic neuroendocrine carcinoma", "shortest_name_length": 57}
{"curie": "MONDO:0001866", "names": ["bipolar i disorder", "Bipolar I disorder", "bipolar I disorder", "Bipolar 1 disorder", "bipolar 1 disorder", "disorder; bipolar, I", "bipolar; disorder, I", "bipolar type I disorder", "Depressed bipolar I disorder", "Bipolar I disorder (disorder)", "Bipolar I disorder (diagnosis)", "Depressed bipolar I disorder, NOS", "Depressed bipolar I disorder (disorder)", "Manic-depressive illness, depressive type", "Manic-depressive psychosis, depressed type", "Bipolar I disorder, most recent episode depressed", "bipolar I disorder, most recent episode, depressed", "Bipolar affective disorder, depressed, unspecified degree", "bipolar I disorder, most recent episode, depressed (diagnosis)", "Bipolar I disorder, Current or most recent episode depressed, Unspecified", "Bipolar I disorder, most recent episode (or current) depressed, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bipolar I disorder", "shortest_name_length": 18}
{"curie": "MONDO:0008273", "names": ["HPLE", "Actinic Prurigo", "Hydroa estivale", "ACTINIC PRURIGO", "actinic prurigo", "Actinic prurigo", "hydroa aestivale", "HYDROA AESTIVALE", "Hydroa aestivale", "Familial actinic prurigo", "RECURRENT SUMMER ERUPTION", "Hutchinson summer prurigo", "hutchinson summer prurigo", "Actinic prurigo (disorder)", "HUTCHINSON SUMMER ERUPTION", "Hutchinson's summer prurigo", "Summer prurigo of Hutchinson", "hydroa aestivale (diagnosis)", "Juvenile Spring Eruption of Ears", "juvenile Spring eruption of ears", "JUVENILE SPRING ERUPTION OF EARS", "Polymorphic Light Eruption, Hereditary", "polymorphic Light eruption, hereditary", "POLYMORPHIC LIGHT ERUPTION, HEREDITARY", "Familial polymorphous light eruption of American Indians", "familial polymorphous light eruption of American Indians", "Hereditary polymorphous light eruption of American Indians", "hereditary polymorphous light eruption of American Indians"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "actinic prurigo", "shortest_name_length": 4}
{"curie": "UMLS:C3146270", "names": ["Stage IV Vulvar Cancer", "stage IV vulvar cancer", "Stage IV Vulvar Carcinoma", "stage IV vulvar carcinoma", "Stage IV Vulvar Cancer AJCC v7", "stage IV vulvar cancer AJCC v7", "stage IV vulvar carcinoma AJCC v7", "Stage IV Vulvar Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Vulvar Cancer AJCC v7", "shortest_name_length": 22}
{"curie": "MONDO:0009027", "names": ["cramps, familial adolescent", "CRAMPS, FAMILIAL ADOLESCENT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cramps, familial adolescent", "shortest_name_length": 27}
{"curie": "UMLS:C0342882", "names": ["heterozygous familial hypercholesterolemia", "Heterozygous familial hypercholesterolemia", "Heterozygous familial hypercholesterolaemia", "Familial hypercholesterolemia - heterozygous", "Familial hypercholesterolaemia - heterozygous", "heterozygous familial hypercholesterolemia (diagnosis)", "Familial hypercholesterolemia - heterozygous (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Familial hypercholesterolemia - heterozygous", "shortest_name_length": 42}
{"curie": "UMLS:C3534585", "names": ["Norovirus Infection", "Norovirus infection", "Infection, Norovirus", "Norovirus Infections", "Infections, Norovirus", "Norwalk Virus Infections", "Norwalk virus infections", "Infection caused by Norovirus", "Infection caused by Norovirus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infection caused by Norovirus", "shortest_name_length": 19}
{"curie": "UMLS:C0266304", "names": ["Double Kidney", "Double kidney", "duplex kidney", "Duplex kidney", "Duplex Kidney", "Kidney duplex", "double kidney", "kidney duplex", "duplex kidneys", "Duplex kidneys", "kidney; duplication", "duplication; kidney", "Double Renal Pelvis", "Double kidney (disorder)", "duplex kidney (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Double kidney (disorder)", "shortest_name_length": 13}
{"curie": "MONDO:0025701", "names": ["HLD22", "hypomyelinating leukodystrophy 22", "leukodystrophy, hypomyelinating, 22", "LEUKODYSTROPHY, HYPOMYELINATING, 22"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukodystrophy, hypomyelinating, 22", "shortest_name_length": 5}
{"curie": "UMLS:C1721098", "names": ["Replication Error Phenotype", "Replication Error Phenotypes", "Error Phenotype, Replication", "Phenotype, Replication Error", "Error Phenotypes, Replication", "Phenotypes, Replication Error"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Replication Error Phenotype", "shortest_name_length": 27}
{"curie": "UMLS:C0156677", "names": ["Antepartum eclampsia", "eclampsia; pregnancy", "pregnancy; eclampsia", "Eclampsia, antepartum", "Eclampsia in pregnancy", "eclampsia in pregnancy", "Eclampsia - not delivered", "Eclampsia in pregnancy (disorder)", "eclampsia in pregnancy (diagnosis)", "Eclampsia, antepartum condition or complication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eclampsia in pregnancy", "shortest_name_length": 20}
{"curie": "MONDO:0043187", "names": ["UAPA", "Absent lung artery", "Pulmonary trunk absent", "Absent pulmonary artery", "pulmonary artery absent", "Pulmonary artery absent", "Missing pulmonary artery", "pulmonary artery agenesis", "Pulmonary artery agenesis", "absence; artery, pulmonary", "artery; absence, pulmonary", "agenesis; artery, pulmonary", "artery; agenesis, pulmonary", "Aplasia of pulmonary artery", "Agenesis of pulmonary artery", "agenesis of pulmonary artery", "Absence of the pulmonary artery", "Unilateral Pulmonary Artery Absence", "Unilateral pulmonary artery agenesis", "congenital absence of pulmonary artery", "Congenital absence of pulmonary artery", "Agenesis of pulmonary artery (disorder)", "agenesis of pulmonary artery (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary artery agenesis", "shortest_name_length": 4}
{"curie": "MONDO:0013979", "names": ["CILD19", "primary ciliary dyskinesia 19", "CILIARY DYSKINESIA, PRIMARY, 19", "ciliary dyskinesia, primary, 19", "LRRC6 primary ciliary dyskinesia", "primary ciliary dyskinesia type 19", "ciliary dyskinesia, primary, type 19", "primary ciliary dyskinesia caused by mutation in LRRC6", "primary ciliary dyskinesia 19 with or without situs inversus", "CILIARY DYSKINESIA, PRIMARY, 19, WITH OR WITHOUT SITUS INVERSUS", "ciliary dyskinesia, primary, 19, with or without situs inversus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia 19", "shortest_name_length": 6}
{"curie": "MONDO:0032810", "names": ["OOMD7", "oocyte maturation defect 7", "OOCYTE MATURATION DEFECT 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oocyte maturation defect 7", "shortest_name_length": 5}
{"curie": "MONDO:0004314", "names": ["Malignant Granular Cell Skin Tumor", "malignant granular cell skin tumor", "malignant granular cell skin tumour", "malignant granular cell skin neoplasm", "malignant granular cell tumor of skin", "Malignant Granular Cell Tumor of Skin", "Malignant Granular Cell Skin Neoplasm", "malignant granular cell tumour of skin", "malignant cutaneous granular cell tumor", "Cutaneous Malignant Granular Cell Tumor", "Malignant Cutaneous Granular Cell Tumor", "malignant granular cell neoplasm of skin", "Malignant Granular Cell Neoplasm of Skin", "Malignant Granular Cell Tumor of the Skin", "malignant granular cell tumor of the skin", "malignant granular cell neoplasm of the skin", "Malignant Granular Cell Neoplasm of the Skin", "malignant cutaneous granular cell skin tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant cutaneous granular cell skin tumor", "shortest_name_length": 34}
{"curie": "MONDO:0015610", "names": ["Acquired aplastic anemia", "acquired aplastic anemia", "Acquired aplastic anaemia", "Acquired aplastic anemia, NOS", "rare acquired aplastic anemia", "Acquired aplastic anaemia, NOS", "Acquired aplastic anemia (disorder)", "Idiopathic acquired aplastic anemia", "Idiopathic acquired aplastic anaemia", "acquired aplastic anemia (diagnosis)", "Aplastic anemia, idiopathic, acquired", "Idiopathic acquired aplastic anemia, NOS", "Idiopathic acquired aplastic anaemia, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired aplastic anemia", "shortest_name_length": 24}
{"curie": "MONDO:0002905", "names": ["mutism", "MUTISM", "Mutism", "Mutisms", "Muteness", "muteness", "Mutism (finding)", "mutism (disease)", "Inability to speak"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mutism", "shortest_name_length": 6}
{"curie": "MONDO:0011370", "names": ["STGD4", "Stargardt disease 4", "Stargardt disease-4", "STARGARDT DISEASE 4", "PROM1 Stargardt disease", "Stargardt disease type 4", "Stargardt disease-4 (diagnosis)", "Stargardt disease caused by mutation in PROM1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stargardt disease 4", "shortest_name_length": 5}
{"curie": "UMLS:C5197664", "names": ["KSHV Muticentric Castleman Disease", "HHV8 Multicentric Castleman Disease", "HHV8-Positive Multicentric Castleman Disease", "KSHV-Associated Multicentric Castleman Disease", "HHV-8-associated multicentric Castleman disease", "HHV-8-Associated Multicentric Castleman Disease", "Kaposi Sarcoma HHV-Associated Multicentric Castleman Disease", "Human herpesvirus-8-associated multicentric Castleman disease", "Kaposi Sarcoma Virus-Associated Multicentric Castleman Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HHV-8-Associated Multicentric Castleman Disease", "shortest_name_length": 34}
{"curie": "MONDO:0014149", "names": ["LCCS5", "lethal congenital contracture syndrome 5", "LETHAL CONGENITAL CONTRACTURE SYNDROME 5", "lethal congenital contracture syndrome type 5", "Lethal congenital contracture syndrome type 5", "myopathy, centronuclear, lethal, autosomal recessive", "MYOPATHY, CENTRONUCLEAR, LETHAL, AUTOSOMAL RECESSIVE", "fetal akinesia-cerebral and retinal hemorrhage syndrome", "Fetal akinesia-cerebral and retinal hemorrhage syndrome", "Fetal akinesia, cerebral and retinal hemorrhage syndrome", "Fetal akinesia, cerebral and retinal haemorrhage syndrome", "Foetal akinesia, cerebral and retinal haemorrhage syndrome", "Fetal akinesia, cerebral and retinal hemorrhage syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fetal akinesia-cerebral and retinal hemorrhage syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0015526", "names": ["CISS", "Crisponi syndrome", "Sohar-Crisponi syndrome", "cold-induced sweating syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cold-induced sweating syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0012772", "names": ["Stevenson-Carey syndrome", "STEVENSON-CAREY SYNDROME", "Stevenson-Carey Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stevenson-Carey syndrome", "shortest_name_length": 24}
{"curie": "MONDO:0033548", "names": ["MYODRIF", "congenital myopathy 17", "Myopathy, Congenital, Due to Myod1 Deficiency", "MYOPATHY, CONGENITAL, DUE TO MYOD1 DEFICIENCY", "MYOPATHY, CONGENITAL, WITH DIAPHRAGMATIC DEFECTS, RESPIRATORY INSUFFICIENCY, AND DYSMORPHIC FACIES", "myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies", "shortest_name_length": 7}
{"curie": "MONDO:0018316", "names": ["fatal post-viral neurodegenerative disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fatal post-viral neurodegenerative disorder", "shortest_name_length": 43}
{"curie": "MONDO:0019883", "names": ["trisomy 9qter", "Trisomy 9qter", "Distal trisomy 9q", "distal trisomy 9q", "Distal duplication 9q", "distal duplication 9q", "distal trisomy type 9q", "telomeric duplication 9q", "Telomeric duplication 9q", "partial trisomy 9q distal", "Distal trisomy 9q (disorder)", "Distal trisomy 9q (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal trisomy 9q", "shortest_name_length": 13}
{"curie": "MONDO:0006676", "names": ["Kakkè", "Beriberi", "BERIBERI", "beriberi", "Beri-beri", "Beri beri", "Beri Beri", "beri-beri", "bery bery", "beri beri", "Beriberi NOS", "Beriberi, NOS", "Beriberi (disorder)", "thiamine deficiency", "Thiamine Deficiency", "endemic polyneuritis", "beriberi (diagnosis)", "POLYNEURITIS, ENDEMIC", "vitamin B1 deficiency", "Vitamin B1 Deficiency", "thiamine deficiency disease", "deficiency; vitamin, B1, beriberi", "vitamin; deficiency, B1, beriberi", "vitamin; deficiency, thiamine, beriberi", "deficiency; vitamin, thiamine, beriberi"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "beriberi", "shortest_name_length": 5}
{"curie": "MONDO:0012937", "names": ["DBA6", "Aase-Smith syndrome 2", "Aase Smith syndrome 2", "AASE-SMITH SYNDROME II", "Aase-Smith Syndrome II", "Diamond-Blackfan anemia 6", "Diamond-Blackfan Anemia 6", "DIAMOND-BLACKFAN ANEMIA 6", "RPL5 Diamond-Blackfan anemia", "Diamond-Blackfan Anemia type 6", "RPL5-related Diamond-Blackfan anemia", "Anemia congenital erythroid hypoplastic", "Aregenerative anemia, chronic congenital", "Anemia, Congenital Erythroid Hypoplastic", "Diamond-Blackfan anemia caused by mutation in RPL5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diamond-Blackfan anemia 6", "shortest_name_length": 4}
{"curie": "MONDO:0017375", "names": ["antenatal enterovirus infection", "Antenatal enterovirus infection", "congenital enterovirus infection", "Congenital enterovirus infection", "congenital enterovirus infectious disease", "Congenital infection caused by enterovirus", "congenital infection caused by enterovirus", "Mother-to-child transmission of enterovirus infection", "Congenital infection caused by enterovirus (disorder)", "mother-to-child transmission of enterovirus infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital enterovirus infection", "shortest_name_length": 31}
{"curie": "MONDO:0043693", "names": ["liver; alcohol", "alcohol; liver", "Hepatopathy alcoholic", "ALCOHOLIC LIVER DAMAGE", "Alcoholic liver damage", "alcoholic damage liver", "alcoholic liver damage", "alcoholic disease liver", "LIVER DISEASE ALCOHOLIC", "ALCOHOLIC LIVER DISEASE", "Alcoholic liver disease", "alcoholic liver disease", "Alcoholic Liver Disease", "alcoholics disease liver", "Liver Disease, Alcoholic", "liver; damage, alcoholic", "alcoholic liver diseases", "Alcoholic Liver Diseases", "liver disease, alcoholic", "alcoholic diseases liver", "damage; liver, alcoholic", "Alcoholic liver diseases", "alcoholic liver disorder", "liver; disease, alcoholic", "Liver Diseases, Alcoholic", "Alcoholic liver disease NOS", "Alcoholic liver damage, NOS", "Alcoholic liver disease, NOS", "ALD - Alcoholic liver disease", "alcohol induced liver disorder", "Alcoholic liver damage (disorder)", "alcoholic liver damage (diagnosis)", "alcoholic liver disease (diagnosis)", "Alcoholic liver damage, unspecified", "Alcoholic liver disease, unspecified", "disease (or disorder); liver, alcoholic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alcoholic liver diseases", "shortest_name_length": 14}
{"curie": "UMLS:C0751717", "names": ["Juvenile Neuroaxonal Dystrophy", "Neuroaxonal Dystrophy, Juvenile", "Dystrophy, Juvenile Neuroaxonal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Juvenile Neuroaxonal Dystrophy", "shortest_name_length": 30}
{"curie": "MONDO:0044718", "names": ["PLDECO", "alkaline ceramidase 3 deficiency", "Alkaline ceramidase 3 deficiency", "leukodystrophy, progressive, early childhood-onset", "LEUKODYSTROPHY, PROGRESSIVE, EARLY CHILDHOOD-ONSET", "leukodystrophy due to alkaline ceramidase 3 deficiency", "Leukodystrophy due to alkaline ceramidase 3 deficiency", "Leucodystrophy due to alkaline ceramidase 3 deficiency", "ACER3-related early childhood-onset progressive leukodystrophy", "ACER3-related early childhood-onset progressive leucodystrophy", "Leukodystrophy due to alkaline ceramidase 3 deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alkaline ceramidase 3 deficiency", "shortest_name_length": 6}
{"curie": "MONDO:0013089", "names": ["SCZD13", "schizophrenia 13", "SCHIZOPHRENIA 13", "schizophrenia, susceptibility to, 13", "schizophrenia, Neurophysiologic defect 1N", "SCHIZOPHRENIA SUSCEPTIBILITY LOCUS, CHROMOSOME 15q13-q14-RELATED", "schizophrenia susceptibility locus, chromosome 15Q13-q14-related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schizophrenia 13", "shortest_name_length": 6}
{"curie": "UMLS:C5670393", "names": ["Floating Rib", "Non-articulated Supernumerary Rib", "SUPERNUMERARY RIB, NON-ARTICULATED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-articulated Supernumerary Rib", "shortest_name_length": 12}
{"curie": "UMLS:C0863194", "names": ["Resectable Hepatoma", "Hepatoma resectable", "Carcinoma liver resectable", "Liver carcinoma resectable", "Malignant hepatoma resectable", "Resectable Liver Cell Carcinoma", "Liver cell carcinoma resectable", "Resectable Hepatocellular Cancer", "Resectable Carcinoma of Liver Cell", "Hepatocellular carcinoma resectable", "Resectable Hepatocellular Carcinoma", "Hepatocellular Carcinoma, Resectable", "Resectable Carcinoma of the Liver Cell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carcinoma liver resectable", "shortest_name_length": 19}
{"curie": "MONDO:0017991", "names": ["TA", "Takayasu", "TAKAYASU DISEASE", "Takayasu Disease", "Takayasu disease", "takayasu disease", "Primary arteritis", "takayasu syndrome", "Takayasu Syndrome", "Disease, Takayasu", "pulseless disease", "PULSELESS DISEASE", "Aortitis Syndrome", "Pulseless disease", "Aortitis syndrome", "Pulseless Disease", "Takayasu arteritis", "pulseless; disease", "takayasu arteritis", "TAKAYASU ARTERITIS", "ARTERITIS TAKAYASU", "Takayasu's disease", "MARTORELL SYNDROME", "Syndrome, Aortitis", "Martorell syndrome", "arteritis takayasu", "Takayasu's Disease", "takayasu's disease", "disease; pulseless", "Takayasu Arteritis", "TAKAYASUS ARTERITIS", "Takayasu's syndrome", "Arteritis, Takayasu", "Idiopathic aortitis", "idiopathic aortitis", "Takayasus Arteritis", "Reverse coarctation", "takayasus arteritis", "ARTERITIS, TAKAYASU", "Aortic arch syndrome", "aortic arch syndrome", "Takayasu's Arteritis", "Aortic Arch Syndrome", "arteritis takayasu's", "Takayasu's arteritis", "AORTIC ARCH SYNDROME", "takayasu's arteritis", "Arteritis, Takayasus", "cervical aortic arch", "Atypical coarctation", "Syndrome, Aortic Arch", "aortic arch; syndrome", "syndrome; aortic arch", "Arteritis, Takayasu's", "Nonspecific arteritis", "Aortic arch arteritis", "arteritis takayasus's", "Aortic Arch Syndromes", "TAKAYASU ARTERIOPATHY", "aortic arch arteritis", "aortic arch; arteritis", "Syndromes, Aortic Arch", "YOUNG FEMALE ARTERITIS", "Middle aortic syndrome", "Young Female Arteritis", "middle aortic syndrome", "arteritis; aortic arch", "Young female arteritis", "Raeder-Harbitz syndrome", "Arteritis, Young Female", "Female Arteritis, Young", "Takayasu's arteriopathy", "Acquired aortoarteritis", "Young Female Arteritides", "BRACHIOCEPHALIC ISCHEMIA", "Female Arteritides, Young", "Arteritides, Young Female", "Nonspecific aortoarteritis", "Takayasu's disease (disorder)", "Occlusive thromboarteriopathy", "Reversed coarctation syndrome", "Idiopathic aortitis (disorder)", "Takayasu's disease (diagnosis)", "Aortic arch syndrome [Takayasu]", "Sclerosing aortitis and arteritis", "Sclerosing aortitis AND arteritis", "pharyngeal arch artery syndromic disease", "Idiopathic medial aortopathy and arteriopathy", "Idiopathic medial aortopathy AND arteriopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Takayasu arteritis", "shortest_name_length": 2}
{"curie": "UMLS:C5236958", "names": ["Unresectable Ampulla of Vater Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Ampulla of Vater Carcinoma", "shortest_name_length": 39}
{"curie": "UMLS:C4511908", "names": ["Intestinal-type adenoma", "Adenoma, Intestinal-Type", "GI Adenoma, Intestinal-Type", "GI Tract Adenoma, Intestinal-Type", "Digestive System Adenoma, Intestinal-Type", "Gastrointestinal Tract Adenoma, Intestinal-Type", "Intestinal-type adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal-type adenoma", "shortest_name_length": 23}
{"curie": "UMLS:C2981620", "names": ["Stage IIIC Hepatocellular Cancer", "Stage IIIC Hepatocellular Carcinoma", "stage IIIC adult primary liver cancer", "Stage IIIC Hepatocellular Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Hepatocellular Carcinoma AJCC v7", "shortest_name_length": 32}
{"curie": "UMLS:C4330844", "names": ["Nutritional Hypophosphatemic Rickets"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nutritional Hypophosphatemic Rickets", "shortest_name_length": 36}
{"curie": "MONDO:0100371", "names": ["Acute hepatitis C", "Acute Hepatitis C", "acute hepatitis C", "acute hepatitis c", "Hepatitis C Acute", "acute c hepatitis", "Hepatitis C, acute", "Acute hepatitis C NOS", "Acute Hepatitis C Infection", "acute hepatitis C infection", "Acute hepatitis C (disorder)", "acute type C viral hepatitis", "acute hepatitis C virus infection", "acute viral hepatitis C infection", "acute hepatitis C infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute hepatitis C virus infection", "shortest_name_length": 17}
{"curie": "UMLS:C4688312", "names": ["Central Nervous System B-Cell Non-Hodgkin Lymphoma", "B-Cell Primary Central Nervous System Non-Hodgkin Lymphoma", "Primary Central Nervous System B-Cell Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System B-Cell Non-Hodgkin Lymphoma", "shortest_name_length": 50}
{"curie": "MONDO:0004211", "names": ["L-Cell Glucagon-Like Peptide-Producing NET", "L-cell glucagon-like peptide-producing NET", "L-cell glucagon-like peptide producing tumor", "L-Cell Glucagon-Like Peptide-Producing Neuroendocrine Tumor", "L-cell glucagon-like peptide-producing neuroendocrine tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "L-cell glucagon-like peptide-producing neuroendocrine tumor", "shortest_name_length": 42}
{"curie": "MONDO:0009786", "names": ["OPA6", "OPTIC ATROPHY 6", "Optic atrophy 6", "optic atrophy 6", "OPTIC ATROPHY 6 (disorder)", "optic atrophy, congenital or early infantile, autosomal recessive", "OPTIC ATROPHY, CONGENITAL OR EARLY INFANTILE, AUTOSOMAL RECESSIVE", "Optic atrophy, congenital or early infantile, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "optic atrophy 6", "shortest_name_length": 4}
{"curie": "MONDO:0014518", "names": ["BDPLT19", "platelet-type bleeding disorder 19", "bleeding disorder, platelet-type, 19", "BLEEDING DISORDER, PLATELET-TYPE, 19", "severe autosomal recessive macrothrombocytopenia", "PRKACG isolated hereditary giant platelet disorder", "isolated hereditary giant platelet disorder caused by mutation in PRKACG"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "platelet-type bleeding disorder 19", "shortest_name_length": 7}
{"curie": "UMLS:C1334666", "names": ["Mediastinal Malignant Non-Seminomatous Germ Cell Tumor", "Malignant Mediastinal Nongerminomatous Germ Cell Tumor", "Malignant Mediastinal Non-Seminomatous Germ Cell Tumor", "Non-Seminomatous Malignant Germ Cell Tumor of Mediastinum", "Mediastinal Malignant Non-Seminomatous Germ Cell Neoplasm", "Non-Seminomatous Malignant Germ Cell Neoplasm of Mediastinum", "Non-Seminomatous Malignant Germ Cell Tumor of the Mediastinum", "Non-Seminomatous Malignant Germ Cell Neoplasm of the Mediastinum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Mediastinal Nongerminomatous Germ Cell Tumor", "shortest_name_length": 54}
{"curie": "MONDO:0014748", "names": ["SEMDFA", "spondyloepimetaphyseal dysplasia, faden-Alkuraya type", "SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE", "spondyloepimetaphyseal dysplasia, faden-ALKURAYA type", "Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome", "progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome", "Progressive spondyloepimetaphyseal dysplasia, short stature, short fourth metatarsals, intellectual disability syndrome", "Progressive spondyloepimetaphyseal dysplasia, short stature, short fourth metatarsals, intellectual disability syndrome (disorder)", "spondyloepimetaphyseal dysplasia, progressive, with short stature, Facial Dysmorphism, short fourth metatarsals, and mental retardation, with or without craniosynostosis", "SPONDYLOEPIMETAPHYSEAL DYSPLASIA, PROGRESSIVE, WITH SHORT STATURE, FACIAL DYSMORPHISM, SHORT FOURTH METATARSALS, AND MENTAL RETARDATION, WITH OR WITHOUT CRANIOSYNOSTOSIS", "spondyloepimetaphyseal dysplasia, progressive, with short stature, Facial Dysmorphism, short fourth metatarsals, and intellectual disability, with or without craniosynostosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0002637", "names": ["reticulosis", "reticuloses", "Reticulosis", "HISTIOCYTOSES", "histiocytosis", "histiocytoses", "Histiocytoses", "Histiocytosis", "Reticulosis, NOS", "Histiocytosis, NOS", "Histiocytic Syndrome", "histiocytic syndrome", "Histiocytic reaction", "Reticulohistiocytosis", "Histiocytic Infiltrate", "Histiocytic infiltrate", "histiocytic infiltrate", "chronic histiocytosis X", "chronic Histiocytosis X", "histiocytoses (diagnosis)", "Histiocytic reaction, NOS", "Histiocytic infiltrate, NOS", "hand Schuller Christian disease", "Hand Schuller Christian disease", "Reticuloendothelial cell infiltrate", "Histiocytosis (morphologic abnormality)", "Reticuloendothelial cell infiltrate, NOS", "histiocytic and dendritic cell neoplasms", "Histiocytic infiltrate (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "histiocytosis", "shortest_name_length": 11}
{"curie": "MONDO:0017739", "names": ["disorder of lysosomal-related organelles"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of lysosomal-related organelles", "shortest_name_length": 40}
{"curie": "UMLS:C3897529", "names": ["Stage IIIB Primary Peritoneal Cancer", "Stage IIIB Primary Peritoneal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Primary Peritoneal Cancer AJCC v7", "shortest_name_length": 36}
{"curie": "UMLS:C4726620", "names": ["Distal Esophagus Adenocarcinoma", "Adenocarcinoma of the Lower Third of the Esophagus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Distal Esophagus Adenocarcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0015415", "names": ["Orbitofacial cleft", "oblique facial cleft"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oblique facial cleft", "shortest_name_length": 18}
{"curie": "UMLS:C5238882", "names": ["Thoracotomy scar", "Thoracotomy Scar"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thoracotomy Scar", "shortest_name_length": 16}
{"curie": "MONDO:0100399", "names": ["AML, t(3;3)(q26;q21)", "AML, t(3;3)(q21;q26.2)", "AML, t(3;3)(q21.3q26.2)", "AML, t(3;3)(q21.3;q26.2)", "acute myeloid leukemia, t(3;3)(q21.3;q26.2)", "Acute Myeloid Leukemia with t(3;3)(q21;q26.2); RPN1-EVI1", "AML with inv(3)(q21;q26.2) or t(3;3) (q21;q26.2);RPNI-EVI1", "Acute Myeloid Leukemia with t(3;3) (q21.3;q26.2); GATA2, MECOM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, t(3;3)(q21.3;q26.2)", "shortest_name_length": 20}
{"curie": "UMLS:C0744620", "names": ["HEAD NECK CANCER SQUAMOUS CELL METASTATIC", "Metastatic Head and Neck Squamous Cell Cancer", "Metastatic Head and Neck Squamous Cell Carcinoma", "Squamous cell carcinoma of head and neck metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Squamous cell carcinoma of head and neck metastatic", "shortest_name_length": 41}
{"curie": "MONDO:0800117", "names": ["cutaneous botryomycosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous botryomycosis", "shortest_name_length": 23}
{"curie": "UMLS:C5420042", "names": ["Sinonasal Pleomorphic Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Pleomorphic Adenoma", "shortest_name_length": 29}
{"curie": "MONDO:0012540", "names": ["ARMD4", "age related macular degeneration 4", "Age-Related Macular Degeneration-4", "CFH age-related macular degeneration", "MACULAR DEGENERATION, AGE-RELATED, 4", "Macular Degeneration, Age-Related, 4", "macular degeneration, age-related, 4", "age related macular degeneration type 4", "macular Degeneration, age-related, type 4", "MACULAR DEGENERATION, AGE-RELATED, 4 (disorder)", "age-related macular degeneration caused by mutation in CFH"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "age related macular degeneration 4", "shortest_name_length": 5}
{"curie": "MONDO:0032845", "names": ["SPGF39", "SPERMATOGENIC FAILURE 39", "spermatogenic failure 39"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 39", "shortest_name_length": 6}
{"curie": "MONDO:0013905", "names": ["SCAR13", "autosomal recessive spinocerebellar ataxia 13", "spinocerebellar ataxia, autosomal recessive 13", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13", "Autosomal recessive spinocerebellar ataxia type 13", "autosomal recessive spinocerebellar ataxia type 13", "spinocerebellar ataxia, autosomal recessive type 13", "Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency", "autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency", "GRM1 autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome", "Autosomal recessive congenital cerebellar ataxia due to metabotropic glutamate receptor 1 deficiency", "autosomal recessive congenital cerebellar ataxia due to metabotropic glutamate receptor 1 deficiency", "GRM1 autosomal recessive cerebellar ataxia - pyramidal signs - nystagmus - oculomotor apraxia syndrome", "autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome caused by mutation in GRM1", "autosomal recessive cerebellar ataxia - pyramidal signs - nystagmus - oculomotor apraxia syndrome caused by mutation in GRM1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive spinocerebellar ataxia 13", "shortest_name_length": 6}
{"curie": "MONDO:0012145", "names": ["ARMD3", "HNARMD", "macular degeneration, age-related, 3", "Macular Degeneration, Age-Related, 3", "MACULAR DEGENERATION, AGE-RELATED, 3", "FBLN5 age-related macular degeneration", "macular Degeneration, age-related, type 3", "age-related macular degeneration caused by mutation in FBLN5", "neuropathy, hereditary, with or without age-related macular Degeneration", "neuropathy, hereditary, with or without age-related macular degeneration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macular degeneration, age-related, 3", "shortest_name_length": 5}
{"curie": "UMLS:C3274142", "names": ["Small Intestinal EC-Cell Serotonin-Producing NET", "Small Intestinal EC-Cell Serotonin-Producing Neuroendocrine Tumor", "Small Intestinal Enterochromaffin Cell Serotonin-Producing Neuroendocrine Tumor", "Small Intestinal Enterochromaffin Cell, Serotonin-Producing Neuroendocrine Tumor", "Small Intestinal Enterochromaffin Cell (EC-Cell), Serotonin-Producing Neuroendocrine Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Intestinal Enterochromaffin Cell Serotonin-Producing Neuroendocrine Tumor", "shortest_name_length": 48}
{"curie": "MONDO:0007695", "names": ["HAIRY PALMS AND SOLES", "hairy palms and soles", "Hairy palms and soles", "circumscribed hairy Dysembryoplasia of palms", "CIRCUMSCRIBED HAIRY DYSEMBRYOPLASIA OF PALMS", "Circumscribed hairy dysembryoplasia of palms", "Hairy cutaneous malformations of palms and soles", "hairy cutaneous malformations of palms and soles", "thickened hair-bearing skin on the palms of both hands", "Thickened hair-bearing skin on the palms of both hands"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hairy palms and soles", "shortest_name_length": 21}
{"curie": "UMLS:C2987263", "names": ["Esophageal Large Cell NEC", "Esophageal Large Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Large Cell Neuroendocrine Carcinoma", "shortest_name_length": 25}
{"curie": "UMLS:C0278479", "names": ["Dukes B colon cancer", "dukes b colon cancer", "cancer colon ii stage", "Stage II Colon Cancer", "stage II colon cancer", "colon cancer, Dukes B", "stage ii colon cancer", "Colon cancer stage II", "colon cancer stage ii", "Colon cancer, stage 2", "colon cancer, stage II", "Dukes B Colon Carcinoma", "COLON NOS CANCER DUKES B", "Colon carcinoma stage II", "Carcinoma colon stage II", "Dukes B Colonic Carcinoma", "Dukes B Carcinoma of Colon", "carcinoma of colon, stage II", "Carcinoma of colon, stage II", "Cancer of the colon, stage 2", "Stage II Colon Cancer AJCC v6", "AJCC Stage II Colon Cancer v6", "Colon Cancer Stage II AJCC v6", "Dukes B Carcinoma of the Colon", "Stage II Cancer of Colon AJCC v6", "Stage II Colon Carcinoma AJCC v6", "Stage II Colonic Carcinoma AJCC v6", "Stage II Carcinoma of Colon AJCC v6", "Stage II Cancer of the Colon AJCC v6", "Carcinoma of colon, stage II (finding)", "Stage II Carcinoma of the Colon AJCC v6", "carcinoma of colon, stage II (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Colon Cancer", "shortest_name_length": 20}
{"curie": "MONDO:0011548", "names": ["Acp", "ataxic cerebral palsy", "cerebral palsy ataxic", "cerebral palsy, ataxic, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral palsy, ataxic, autosomal recessive", "shortest_name_length": 3}
{"curie": "MONDO:0001121", "names": ["Frontal Sinusitis", "frontal sinusitis", "Frontal sinusitis", "FRONTAL SINUSITIS", "Sinusitis, Frontal", "Frontal Sinusitides", "Sinusitides, Frontal", "Frontal sinusitis NOS", "Frontal sinusitis, NOS", "sinusitis; frontal sinus", "frontal sinus; sinusitis", "Frontal sinusitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontal sinusitis", "shortest_name_length": 17}
{"curie": "MONDO:0032594", "names": ["IDDRP", "INTELLECTUAL DEVELOPMENTAL DISORDER AND RETINITIS PIGMENTOSA", "intellectual developmental disorder and retinitis pigmentosa; IDDRP"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder and retinitis pigmentosa; IDDRP", "shortest_name_length": 5}
{"curie": "UMLS:C5420762", "names": ["Conjunctival Pseudoepitheliomatous Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conjunctival Pseudoepitheliomatous Hyperplasia", "shortest_name_length": 46}
{"curie": "UMLS:C2981716", "names": ["stage IIA mycosis fungoides/Sezary syndrome", "Stage IIA Mycosis Fungoides and Sezary Syndrome", "Stage IIA Mycosis Fungoides and Sézary Syndrome", "Stage IIA Mycosis Fungoides and Sezary Syndrome AJCC v7", "stage IIA mycosis fungoides and Sezary syndrome AJCC v7", "Stage IIA Mycosis Fungoides and Sézary Syndrome AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Mycosis Fungoides and Sezary Syndrome AJCC v7", "shortest_name_length": 43}
{"curie": "UMLS:C0235395", "names": ["fluid loss", "Fluid loss", "FLUID LOSS", "fluid; loss", "loss; fluid", "loss of fluid", "LOSS OF FLUIDS", "Loss of fluid, NOS", "Fluid loss (observable entity)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fluid loss", "shortest_name_length": 10}
{"curie": "MONDO:0008172", "names": ["PHOAD", "PDP, AUTOSOMAL DOMINANT", "PDP, autosomal dominant", "PHO, AUTOSOMAL DOMINANT", "Pho, autosomal dominant", "Autosomal Dominant Pachydermoperiostosis", "Autosomal Dominant Pachydermoperiostoses", "Pachydermoperiostoses, Autosomal Dominant", "PACHYDERMOPERIOSTOSIS, AUTOSOMAL DOMINANT", "Pachydermoperiostosis, Autosomal Dominant", "pachydermoperiostosis, autosomal dominant", "Primary Hypertrophic Osteoarthropathy, Autosomal Dominant", "Hypertrophic Osteoarthropathy, Primary, Autosomal Dominant", "hypertrophic osteoarthropathy, primary, autosomal dominant", "HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL DOMINANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophic osteoarthropathy, primary, autosomal dominant", "shortest_name_length": 5}
{"curie": "MONDO:0019606", "names": ["cryoglobulinemia type 1", "simple cryoglobulinemia", "Cryoglobulinemia type 1", "cryoglobulinemia simple", "Simple cryoglobulinemia", "Simple cryoglobulinaemia", "Cryoglobulinaemia type 1", "Simple cryoglobulinemia (disorder)", "Simple cryoglobulinemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "simple cryoglobulinemia", "shortest_name_length": 23}
{"curie": "UMLS:C5418914", "names": ["Refractory Fallopian Tube Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Fallopian Tube Adenocarcinoma", "shortest_name_length": 40}
{"curie": "UMLS:C0858524", "names": ["Tachycardia nervous"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tachycardia nervous", "shortest_name_length": 19}
{"curie": "MONDO:0010584", "names": ["DKCX", "ZINSSER-COLE-ENGMAN SYNDROME", "Zinsser-Cole-Engman syndrome", "Zinsser Cole Engman Syndrome", "Zinsser-Cole-Engman Syndrome", "Hoyeraal Hreidarsson syndrome", "Syndrome, Zinsser-Cole-Engman", "Hoyeraal Hreidarsson Syndrome", "dyskeratosis congenita X-linked", "X-linked dyskeratosis congenita", "X-Linked Dyskeratosis Congenita", "DYSKERATOSIS CONGENITA, X-LINKED", "Dyskeratosis Congenita, X Linked", "Congenita, X-Linked Dyskeratosis", "Dyskeratosis Congenita, X-Linked", "X-Linked Dyskeratosis Congenitas", "dyskeratosis congenita, X-linked", "cerebellar hypoplasia with pancytopenia", "X-linked dyskeratosis congenita (disorder)", "dyskeratosis congenita, X-linked, X-linked recessive", "GROWTH RETARDATION, PRENATAL, WITH PROGRESSIVE PANCYTOPENIA AND CEREBELLAR HYPOPLASIA", "Growth retardation, prenatal, with progressive pancytopenia and cerebellar hypoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyskeratosis congenita, X-linked", "shortest_name_length": 4}
{"curie": "UMLS:C1332931", "names": ["Chest Wall Hodgkin Lymphoma", "Chest Wall Hodgkin's Disease", "Chest Wall Hodgkin's Lymphoma", "Hodgkin's Disease of Chest Wall", "Hodgkin's Lymphoma of Chest Wall", "Hodgkin's Disease of the Chest Wall", "Hodgkin's Lymphoma of the Chest Wall", "Primary Chest Wall Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chest Wall Hodgkin Lymphoma", "shortest_name_length": 27}
{"curie": "MONDO:0024171", "names": ["Van Goethem syndrome", "radio-digito-facial dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radio-digito-facial dysplasia", "shortest_name_length": 20}
{"curie": "MONDO:0010514", "names": ["IMD50", "immunodeficiency 50", "IMMUNODEFICIENCY 50", "immunodeficiency type 50", "CID due to Moesin deficiency", "MSN-related combined immunodeficiency", "immunodeficiency 50 X linked recessive", "IMMUNODEFICIENCY 50, X-LINKED RECESSIVE", "immunodeficiency 50, X-linked recessive", "X-linked Moesin-associated immunodeficiency", "X-linked moesin-associated immunodeficiency", "MSN (moesin) related combined immunodeficiency", "combined immunodeficiency due to moesin deficiency", "combined immunodeficiency due to Moesin deficiency", "Combined immunodeficiency due to moesin deficiency", "Combined immunodeficiency due to Moesin deficiency", "Combined immunodeficiency due to moesin deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined immunodeficiency due to moesin deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0007958", "names": ["MTC", "Fmtc", "FMTC", "MTC1", "Mtc1", "familial MTC", "Familial MTC", "medullary thyroid carcinoma", "familial medullary thyroid cancer", "Familial medullary thyroid cancer", "Medullary thyroid cancer, familial", "Thyroid cancer, familial medullary", "hereditary medullary thyroid cancer", "familial medullary thyroid carcinoma", "Familial medullary thyroid carcinoma", "thyroid carcinoma, familial medullary", "THYROID CARCINOMA, FAMILIAL MEDULLARY", "Thyroid Carcinoma, Familial Medullary", "hereditary thyroid medullary carcinoma", "Hereditary Thyroid Gland Medullary Cancer", "Familial Thyroid Gland Medullary Carcinoma", "familial thyroid gland medullary carcinoma", "hereditary thyroid gland medullary carcinoma", "Hereditary Thyroid Gland Medullary Carcinoma", "hereditary medullary thyroid gland carcinoma", "familial medullary carcinoma of thyroid gland", "familial medullary thyroid carcinoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial medullary thyroid carcinoma", "shortest_name_length": 3}
{"curie": "MONDO:0000368", "names": ["Extrapulmonary TB", "TB, extrapulmonary", "TUBERCULOSIS EXTRAPULMONARY", "tuberculosis extrapulmonary", "Extrapulmonary Tuberculosis", "Extrapulmonary tuberculosis", "extrapulmonary tuberculosis", "Extrapulmonary Tuberculoses", "extra-pulmonary tuberculosis", "extra pulmonary tuberculosis", "Extra-Pulmonary Tuberculoses", "Tuberculosis, extrapulmonary", "Tuberculosis, Extrapulmonary", "Extra-Pulmonary Tuberculosis", "Extra Pulmonary Tuberculosis", "Tuberculosis, Extra-Pulmonary", "Tuberculosis, extrapulmonary (disorder)", "extrapulmonary tuberculosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extrapulmonary tuberculosis", "shortest_name_length": 17}
{"curie": "MONDO:0032901", "names": ["CATIFA", "Catifa syndrome", "CATIFA SYNDROME", "CLEFT LIP, CATARACT, TOOTH ABNORMALITY, IMPAIRED INTELLECTUAL DEVELOPMENT, FACIAL DYSMORPHISM, AND ATTENTION-DEFICIT HYPERACTIVITY DISORDER", "Cleft Lip, Cataract, Tooth Abnormality, Impaired Intellectual Development, Facial Dysmorphism, and Attention-Deficit Hyperactivity Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Catifa syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C3272835", "names": ["Colorectal Schwannoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Schwannoma", "shortest_name_length": 21}
{"curie": "UMLS:C4764210", "names": ["Bladder Non-Invasive Papillary Urothelial Carcinoma", "Non-invasive papillary urothelial carcinoma of bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-invasive papillary urothelial carcinoma of bladder", "shortest_name_length": 51}
{"curie": "MONDO:0002745", "names": ["Fallopian Tube Mucinous Tumor", "fallopian tube mucinous tumor", "fallopian tube mucinous neoplasm", "Fallopian Tube Mucinous Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fallopian tube mucinous tumor", "shortest_name_length": 29}
{"curie": "UMLS:C0854828", "names": ["T Cell Lymphoma Stage I", "T-cell lymphoma stage I", "Stage I T Cell Lymphoma", "T-Cell Lymphoma Stage I", "Stage I T-Cell Lymphoma", "T-cell lymphoma NOS stage I", "Stage I T-Cell Non-Hodgkin Lymphoma", "Stage I T-Cell Non-Hodgkin's Lymphoma", "Ann Arbor Stage I T-Cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-cell lymphoma stage I", "shortest_name_length": 23}
{"curie": "UMLS:C2986671", "names": ["Stage III Liver Cancer", "Stage IIIB Adult Liver Cancer AJCC v7", "stage IIIB adult primary liver cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Adult Liver Cancer AJCC v7", "shortest_name_length": 22}
{"curie": "UMLS:C3899659", "names": ["Giant Cell Glioblastoma", "Childhood Giant Cell Glioblastoma", "childhood giant cell glioblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Giant Cell Glioblastoma", "shortest_name_length": 23}
{"curie": "MONDO:0800121", "names": ["cellular interstitial pneumonitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cellular interstitial pneumonitis", "shortest_name_length": 33}
{"curie": "UMLS:C0861748", "names": ["Pancreatic adenocarcinoma resectable", "Resectable Pancreatic Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic adenocarcinoma resectable", "shortest_name_length": 36}
{"curie": "UMLS:C4331291", "names": ["Single Central Incisor Syndrome", "Single Central Maxillary Incisor Syndrome", "Solitary Central Maxillary Incisor Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Single Central Incisor Syndrome", "shortest_name_length": 31}
{"curie": "UMLS:C1557933", "names": ["Spermatic Cord Obstruction", "Spermatic cord obstruction", "spermatic cord obstruction", "spermatic cord obstruction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spermatic cord obstruction", "shortest_name_length": 26}
{"curie": "MONDO:0016191", "names": ["qualitative or quantitative defects of titin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of titin", "shortest_name_length": 44}
{"curie": "UMLS:C4524633", "names": ["Esophageal Adenocarcinoma by AJCC v8 cTNM Stage", "Esophageal Adenocarcinoma by AJCC v8 Clinical Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Adenocarcinoma by AJCC v8 Clinical Stage", "shortest_name_length": 47}
{"curie": "UMLS:C1142183", "names": ["Orbivirus Infection", "Orbivirus infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Orbivirus infection", "shortest_name_length": 19}
{"curie": "UMLS:C0518960", "names": ["Right atrial myxoma", "ATRIAL MYXOMA RIGHT", "right atrial myxoma", "Right Atrial Myxoma", "myxoma of right atrium", "Myxoma of Right Atrium", "Myxoma of the Right Atrium", "myxoma of right atrium (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Right atrial myxoma", "shortest_name_length": 19}
{"curie": "MONDO:0008098", "names": ["NIEVERGELT SYNDROME", "Nievergelt syndrome", "Nievergelt's syndrome", "Nievergelt-Erb syndrome", "Nievergelt's syndrome (disorder)", "Mesomelic dwarfism Nievergelt type", "mesomelic dwarfism Nievergelt type", "mesomelic dwarfism, Nievergelt type", "Mesomelic dwarfism, Nievergelt type", "MESOMELIC DYSPLASIA, NIEVERGELT TYPE", "mesomelic dysplasia, Nievergelt type", "Mesomelic dysplasia, Nievergelt type", "Mesomelic Dysplasia, Nievergelt Type", "Mesomelic dysplasia - Nievergelt type", "Hereditary extremity malformation syndrome", "radioulnar synostosis and a typical rhomboid shape of the tibia and fibula"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mesomelic dwarfism, Nievergelt type", "shortest_name_length": 19}
{"curie": "MONDO:0007743", "names": ["ADHD", "attention deficit/hyperactivity disorder", "Attention Deficit-Hyperactivity Disorder", "attention deficit-hyperactivity disorder", "Attention Deficit Hyperactivity Disorder", "Attention Deficit/Hyperactivity Disorder", "attention deficit hyperactivity disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "attention deficit-hyperactivity disorder", "shortest_name_length": 4}
{"curie": "MONDO:0024891", "names": ["Meningitis noninfective", "Non-infective meningitis", "non-infective meningitis", "non-infectious meningitis", "Non-infective meningitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-infectious meningitis", "shortest_name_length": 23}
{"curie": "MONDO:0017709", "names": ["disorder of lipid absorption and transport"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of lipid absorption and transport", "shortest_name_length": 42}
{"curie": "MONDO:0033557", "names": ["FHL6", "IMDYSHI", "FHL6, FORMERLY", "HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 6", "hemophagocytic lymphohistiocytosis, familial, 6", "HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 6, FORMERLY", "IMMUNE DYSREGULATION AND SYSTEMIC HYPERINFLAMMATION SYNDROME", "immune dysregulation and systemic hyperinflammation syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemophagocytic lymphohistiocytosis, familial, 6", "shortest_name_length": 4}
{"curie": "MONDO:0044657", "names": ["MME-related autosomal dominant CMT2", "MME-related autosomal dominant Charcot Marie Tooth disease type 2", "MME-related autosomal dominant hereditary motor and sensory neuropathy type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MME-related autosomal dominant Charcot Marie Tooth disease type 2", "shortest_name_length": 35}
{"curie": "UMLS:C0161816", "names": ["Complication;heart", "complication heart", "complications heart", "Cardiac complication", "cardiac complication", "complications; heart", "heart; complications", "Cardiac complications", "cardiac complications", "complications cardiac", "complications; cardiac", "cardiac; complications", "Cardiac complication, NOS", "Cardiovascular Complication", "cardiovascular complication", "Cardiovascular complications", "cardiovascular complications", "Cardiac complications of care", "Cardiac complication (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiac complication", "shortest_name_length": 18}
{"curie": "MONDO:0800091", "names": ["overgrowth or tall stature syndrome with skeletal involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "overgrowth or tall stature syndrome with skeletal involvement", "shortest_name_length": 61}
{"curie": "UMLS:C0398554", "names": ["Infantile Pyknocytosis", "Infantile pyknocytosis", "Hereditary Pyknocytosis", "Infantile pyknocytosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infantile pyknocytosis", "shortest_name_length": 22}
{"curie": "UMLS:C1336502", "names": ["Sternal Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sternal Disorder", "shortest_name_length": 16}
{"curie": "MONDO:0012086", "names": ["DFNA31", "autosomal dominant deafness 31", "DEAFNESS, AUTOSOMAL DOMINANT 31", "deafness, autosomal dominant 31", "Deafness, Autosomal Dominant 31", "DEAFNESS, AUTOSOMAL DOMINANT 31 (disorder)", "autosomal dominant nonsyndromic deafness 31", "autosomal dominant nonsyndromic hearing loss 31", "autosomal dominant nonsyndromic deafness type 31"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 31", "shortest_name_length": 6}
{"curie": "MONDO:0013034", "names": ["KPPS2", "SPPK2", "PPKS2", "striate palmoplantar keratoderma 2", "keratosis palmoplantaris striata 2", "KERATOSIS PALMOPLANTARIS STRIATA II", "Striate Palmoplantar Keratoderma II", "STRIATE PALMOPLANTAR KERATODERMA II", "keratosis palmoplantaris striata II", "Keratosis Palmoplantaris Striata II", "DSP striate palmoplantar keratoderma", "keratosis palmoplantaris striata type 2", "keratoderma, palmoplantar, striate form 2", "KERATODERMA, PALMOPLANTAR, STRIATE FORM II", "Keratoderma, Palmoplantar, Striate Form II", "striate palmoplantar keratoderma caused by mutation in DSP"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratosis palmoplantaris striata 2", "shortest_name_length": 5}
{"curie": "UMLS:C0521505", "names": ["RASH INJECTION SITE", "Rash injection site", "Injection site rash", "Rash at site of injection", "Injection site dermatitis", "INJECTION SITE DERMATITIS", "Injection site dermatitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site dermatitis", "shortest_name_length": 19}
{"curie": "MONDO:0009667", "names": ["MDDGA3", "muscle-eye-brain-POMGNT1 related", "congenital muscular dystrophy-dystroglycanopathy type A3", "Walker-Warburg syndrome or muscle-eye-brain disease, POMGNT1-related", "WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMGNT1-RELATED", "congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A3", "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A3", "Muscular Dystrophy-Dystroglycanopathy (Congenital with Brain and Eye Anomalies) Type A, 3", "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type A, 3", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3", "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A3", "shortest_name_length": 6}
{"curie": "MONDO:0009449", "names": ["cilia with defective radial spokes", "Cilia with defective radial spokes", "Ciliary Dyskinesia With Defective Radial Spokes", "ciliary dyskinesia with defective radial spokes", "CILIARY DYSKINESIA WITH DEFECTIVE RADIAL SPOKES", "Immotile cilia syndrome due to defective radial spokes", "Immotile Cilia Syndrome Due To Defective Radial Spokes", "IMMOTILE CILIA SYNDROME DUE TO DEFECTIVE RADIAL SPOKES", "immotile cilia syndrome due to defective radial spokes", "Immotile cilia syndrome, due to defective radial spokes", "immotile cilia syndrome, due to defective radial spokes", "Immotile cilia syndrome due to defective radial spokes (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ciliary dyskinesia with defective radial spokes", "shortest_name_length": 34}
{"curie": "MONDO:0007138", "names": ["ASMD", "ASOD", "ASGD1", "Irido-corneal dysgenesis", "Anterior segment dysgenesis", "ANTERIOR SEGMENT DYSGENESIS 1", "anterior segment dysgenesis 1", "Anterior chamber malformation", "Anterior chamber cleavage defect", "Irido-corneal dysgenesis syndrome", "Anterior segment ocular dysgenesis", "Ocular anterior segment dysgenesis", "Anterior chamber cleavage disorder", "ANTERIOR SEGMENT OCULAR DYSGENESIS", "anterior segment ocular dysgenesis", "Anterior chamber mesodermal anomalies", "Anterior segment developmental anomaly", "Anterior segment mesenchymal dysgenesis", "anterior segment mesenchymal dysgenesis", "ANTERIOR SEGMENT MESENCHYMAL DYSGENESIS", "Anterior segment mesencyhmal dysgenesis", "Anterior segment developmental abnormality", "anterior segment dysgenesis 1, multiple subtypes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anterior segment dysgenesis 1", "shortest_name_length": 4}
{"curie": "UMLS:C4744490", "names": ["Refractory Malignant Peripheral Nerve Sheath Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Malignant Peripheral Nerve Sheath Tumor", "shortest_name_length": 50}
{"curie": "UMLS:C4744363", "names": ["Mixed Gangliocytoma-PitNET", "Mixed Gangliocytoma-PitNET/Adenoma", "Pituitary Gland Mixed Gangliocytoma-Adenoma", "Pituitary Gland Adenoma-Neuronal Choristoma", "Mixed Gangliocytoma-Pituitary Neuroendocrine Tumor", "Pituitary Gland Adenoma with Gangliocytic Component", "Mixed Gangliocytoma-Pituitary Neuroendocrine Tumor/Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mixed Gangliocytoma-Pituitary Neuroendocrine Tumor", "shortest_name_length": 26}
{"curie": "MONDO:0009920", "names": ["AOO SYNDROME", "Aoo syndrome", "Acrootoocular Syndrome", "acrootoocular syndrome", "Acrootoocular syndrome", "ACROOTOOCULAR SYNDROME", "Acro-oto-ocular syndrome", "Acrootoocular syndrome (disorder)", "pseudopapilledema-blepharophimosis-hand anomalies syndrome", "Pseudopapilledema-blepharophimosis-hand anomalies syndrome", "Pseudopapilledema, blepharophimosis and hand anomaly syndrome", "Pseudopapilloedema, blepharophimosis and hand anomaly syndrome", "pseudopapilledema, ocular hypotelorism, blepharophimosis, and hand anomalies", "PSEUDOPAPILLEDEMA, OCULAR HYPOTELORISM, BLEPHAROPHIMOSIS, AND HAND ANOMALIES", "Pseudopapilledema, Ocular Hypotelorism, Blepharophimosis, and Hand Anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acrootoocular syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0013714", "names": ["MBLD", "LCAPD1", "MBL DEFICIENCY", "MBL deficiency", "MBP deficiency", "MBL Deficiency", "MBP Deficiency", "MBP DEFICIENCY", "MBL2 deficiency", "MBL2 DEFICIENCY", "MBL2 Deficiency", "Mannose-Binding Lectin Deficiency", "MANNOSE-BINDING LECTIN DEFICIENCY", "Mannose-binding lectin deficiency", "mannose-binding lectin deficiency", "Mannose-binding protein deficiency", "mannose-binding protein deficiency", "Mannose-Binding Protein Deficiency", "MANNOSE-BINDING PROTEIN DEFICIENCY", "Mannose-Binding Lectin Protein Deficiency", "Mannose-binding lectin protein deficiency", "Mannose-binding lectin deficiency (disorder)", "LECTIN COMPLEMENT ACTIVATION PATHWAY, DEFECT IN, 1", "lectin complement activation pathway, defect in, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mannose-binding lectin deficiency", "shortest_name_length": 4}
{"curie": "UMLS:C0151705", "names": ["Retroperitoneal bleed", "retroperitoneal bleed", "bleeds retroperitoneal", "retroperitoneal bleeding", "bleeding retroperitoneal", "Retroperitoneal bleeding", "Hemorrhage retroperitoneal", "RETROPERITONEAL HEMORRHAGE", "Retroperitoneal hemorrhage", "retroperitoneal hemorrhage", "HEMORRHAGE RETROPERITONEAL", "Retroperitoneal Hemorrhage", "HAEMORRHAGE RETROPERITONEAL", "Haemorrhage retroperitoneal", "Retroperitoneal haemorrhage", "retroperitoneal; hemorrhage", "hemorrhage; retroperitoneal", "retroperitoneal bleeding (diagnosis)", "Retroperitoneal hemorrhage (disorder)", "gastrointestinal bleeding retroperitoneum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retroperitoneal Hemorrhage", "shortest_name_length": 21}
{"curie": "MONDO:0014480", "names": ["SRXY9", "46XY sex reversal 9", "46,XY SEX REVERSAL 9", "46,XY SEX reversal 9", "46,XY sex reversal 9", "46,XY Sex reversal type 9", "46,XY SEX REVERSAL, ZFPM2-RELATED", "46,XY sex reversal, ZFPM2-related", "46,XY Sex reversal, Zfpm2-related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XY sex reversal 9", "shortest_name_length": 5}
{"curie": "MONDO:0009950", "names": ["Pk deficiency", "PK DEFICIENCY", "PK deficiency", "PK Deficiency", "pyruvate kinase deficiency", "PYRUVATE KINASE DEFICIENCY", "deficiency kinase pyruvate", "Pyruvate Kinase Deficiency", "Pyruvate kinase deficiency", "deficiency of pyruvate kinase", "Deficiency of pyruvate kinase", "PK - Pyruvate kinase deficiency", "ANEMIA, HEMOLYTIC, DACIE TYPE II", "Pyruvate Kinase Deficiency of Red Cells", "PYRUVATE KINASE DEFICIENCY OF RED CELLS", "pyruvate kinase deficiency of red cells", "Deficiency of phosphoenolpyruvate kinase", "Deficiency of pyruvate kinase (disorder)", "pyruvate kinase deficiency of erythrocyte", "Pyruvate Kinase Deficiency of Erythrocyte", "deficiency of pyruvate kinase (diagnosis)", "PYRUVATE KINASE DEFICIENCY OF ERYTHROCYTE", "Pyruvate kinase deficiency of erythrocytes", "pyruvate kinase deficiency of erythrocytes", "anemia hemolytic pyruvate kinase deficiency", "Deficiency of phosphoenol transphosphorylase", "ANEMIA, HEMOLYTIC, PYRUVATE KINASE DEFICIENCY", "hemolytic Anemia due to pyruvate Kinase deficiency", "Hemolytic Anemia due to Pyruvate Kinase Deficiency", "anemia hemolytic pyruvate kinase deficiency (diagnosis)", "hemolytic anemia due to red cell pyruvate kinase deficiency", "Hemolytic anemia due to red cell pyruvate kinase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyruvate kinase deficiency of red cells", "shortest_name_length": 13}
{"curie": "UMLS:C1336023", "names": ["solar radiation-related skin melanoma", "Solar Radiation-Related Skin Melanoma", "Solar Radiation-Related Melanoma of Skin", "Solar Radiation-Related Cutaneous Melanoma", "Solar Radiation-Related Melanoma of the Skin", "Solar Radiation-Related Cutaneous (Skin) Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Solar Radiation-Related Cutaneous Melanoma", "shortest_name_length": 37}
{"curie": "MONDO:0012206", "names": ["CZECH DYSPLASIA", "Czech dysplasia", "Czech Dysplasia", "SED with metatarsal shortening", "Czech dysplasia metatarsal type", "CZECH DYSPLASIA, METATARSAL TYPE", "Czech dysplasia, metatarsal type", "Czech dysplasia metatarsal type (disorder)", "Spondyloarthropathy with Short Third and Fourth Toes", "Spondyloepiphyseal dysplasia with metatarsal shortening", "SPONDYLOEPIPHYSEAL DYSPLASIA WITH PRECOCIOUS OSTEOARTHRITIS", "spondyloepiphyseal dysplasia with precocious osteoarthritis", "Progressive Pseudorheumatoid Dysplasia with Hypoplastic Toes", "pseudorheumatoid dysplasia progressive, with hypoplastic toes", "PSEUDORHEUMATOID DYSPLASIA, PROGRESSIVE, WITH HYPOPLASTIC TOES", "pseudorheumatoid dysplasia, progressive, with hypoplastic toes", "Pseudorheumatoid dysplasia, progressive, with hypoplastic toes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Czech dysplasia, metatarsal type", "shortest_name_length": 15}
{"curie": "MONDO:0021013", "names": ["TTD4", "ABHS", "TTDN1", "Clastothrix", "Bamboo hair", "clastothrix", "trichoclasis", "Trichoclasis", "BIDS Syndrome", "BIDS SYNDROME", "BIDS syndrome", "BIDS Syndromes", "Pollitt syndrome", "POLLITT SYNDROME", "Pollitt's syndrome", "HAIR-BRAIN SYNDROME", "Hair Brain Syndrome", "Hair-Brain Syndrome", "hair-brain syndrome", "trichothiodystrophy", "trichorrhexis nodosa", "Trichorrhexis nodosa", "Hair-Brain Syndromes", "nodosa; trichorrhexis", "trichorrhexis; nodosa", "Clastothrix (disorder)", "Bamboo hair (disorder)", "trichorrhexis invaginata", "Trichorrhexis invaginata", "trichothiodystrophy (TTD)", "trichorrhexis; invaginata", "invaginata; trichorrhexis", "amish brittle hair syndrome", "Amish Brittle Hair Syndrome", "Amish brittle hair syndrome", "neurotrichocutaneous syndrome", "Trichorrhexis nodosa syndrome", "trichorrhexis nodosa syndrome", "trichorrhexis nodosa (diagnosis)", "AMISH BRITTLE HAIR BRAIN SYNDROME", "Amish brittle hair brain syndrome", "Amish Brittle Hair Brain Syndrome", "trichorrhexis invaginata (diagnosis)", "nonphotosensitive trichothiodystrophy", "nonphotosensitive trichothiodystrophy 4", "Trichothiodystrophy 4, Nonphotosensitive", "TRICHOTHIODYSTROPHY, NONPHOTOSENSITIVE 1", "Trichothiodystrophy, Nonphotosensitive 1", "trichothiodystrophy 4, nonphotosensitive", "Trichorrhexis invaginata (\"bamboo hair\")", "TRICHOTHIODYSTROPHY 4, NONPHOTOSENSITIVE", "trichothiodystrophy, nonphotosensitive 1", "Trichothiodystrophies, Nonphotosensitive 1", "trichothiodystrophy-neurocutaneous syndrome", "Trichothiodystrophy-neurocutaneous syndrome", "TRICHOTHIODYSTROPHY-NEUROCUTANEOUS SYNDROME", "MPLKIP nonphotosensitive trichothiodystrophy", "Trichothiodystrophy-neurotrichocutaneous syndrome of Pollitt", "nonphotosensitive trichothiodystrophy caused by mutation in MPLKIP", "Brittle hair-impaired intellect-decreased fertility-short stature syndrome", "BIDS brittle hair-impaired intellect-decreased fertility-short stature syndrome", "brittle hair-intellectual impairment-decreased fertility-short stature syndrome", "Brittle Hair Intellectual Impairment Decreased Fertility Short Stature Syndrome", "Brittle Hair-Intellectual Impairment-Decreased Fertility-Short Stature Syndrome", "Brittle hair-impaired intellect-decreased fertility-short stature syndrome (disorder)", "brittle hair-intellectual impairment-decreased fertility-short stature (BIDS) syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichothiodystrophy 4, nonphotosensitive", "shortest_name_length": 4}
{"curie": "MONDO:0016022", "names": ["eme", "EME", "Myoclonic seizure", "myoclonic seizure", "Myoclonus epilepsy", "Myoclonus Epilepsy", "myoclonic seizures", "MYOCLONIC EPILEPSY", "epilepsy myoclonic", "Myoclonic Epilepsy", "myoclonus epilepsy", "Myoclonic epilepsy", "myoclonic epilepsy", "Epilepsy, Myoclonic", "epilepsy; myoclonus", "Epilepsy, Myoclonus", "Myoclonus Epilepsies", "myoclonia epileptica", "Myoclonic Epilepsies", "Epilepsies, Myoclonic", "epileptica; myoclonus", "Myoclonic Seizure Disorder", "Myoclonic seizure disorder", "myoclonic seizure disorder", "Myoclonic Seizure Disorders", "Seizure Disorder, Myoclonic", "Seizure Disorders, Myoclonic", "epileptic seizures, myoclonic", "Epileptic seizures, myoclonic", "Early myoclonic encephalopathy", "Early Myoclonic Encephalopathy", "epileptic seizures - myoclonic", "myoclonic epilepsy (diagnosis)", "Epileptic seizures - myoclonic", "early myoclonic encephalopathy", "generalized convulsive myoclonic seizure", "Early myoclonic encephalopathy (disorder)", "Symptomatic early myoclonic encephalopathy", "Early myoclonic encephalopathy with suppression-bursts", "early myoclonic encephalopathy with suppression-bursts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early myoclonic encephalopathy", "shortest_name_length": 3}
{"curie": "UMLS:C5418811", "names": ["Advanced Endometrial Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Endometrial Serous Adenocarcinoma", "shortest_name_length": 42}
{"curie": "UMLS:C1333060", "names": ["Classic Type Tricholemmoma", "Classic Type Trichilemmoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Classic Type Trichilemmoma", "shortest_name_length": 26}
{"curie": "MONDO:0014696", "names": ["COFS3", "cerebrooculofacioskeletal syndrome 3", "Cerebrooculofacioskeletal Syndrome 3", "CEREBROOCULOFACIOSKELETAL SYNDROME 3", "cerebrooculofacioskeletal syndrome type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebrooculofacioskeletal syndrome 3", "shortest_name_length": 5}
{"curie": "UMLS:C4524250", "names": ["Anembryonic gestation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anembryonic gestation", "shortest_name_length": 21}
{"curie": "MONDO:0002153", "names": ["Telogen effluvium", "TELOGEN EFFLUVIUM", "Telogen Effluvium", "telogen effluvium", "telogen; effluvium", "effluvium; telogen", "Telogen effluvium (disorder)", "telogen effluvium (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "telogen effluvium", "shortest_name_length": 17}
{"curie": "MONDO:0022405", "names": ["retinal ciliopathy due to mutation in nephronophthisis gene"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal ciliopathy due to mutation in nephronophthisis gene", "shortest_name_length": 59}
{"curie": "MONDO:0015717", "names": ["mild hemophilia B", "mild hemophilia type B", "mild factor IX deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mild hemophilia B", "shortest_name_length": 17}
{"curie": "UMLS:C5447399", "names": ["Advanced Lung Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Lung Adenocarcinoma", "shortest_name_length": 28}
{"curie": "UMLS:C0027671", "names": ["neoplastic process", "neoplastic processes", "Neoplastic Processes", "Processes, Neoplastic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplastic Processes", "shortest_name_length": 18}
{"curie": "MONDO:0007527", "names": ["pEDS", "EDS8", "EDS 8", "EDS VIII", "periodontal EDS", "Periodontal EDS", "EDS8 (formerly)", "EDS VIII (formerly)", "Ehlers-Danlos syndrome type 8", "Ehlers-Danlos syndrome, type 8", "Ehlers-Danlos syndrome type VIII", "type VIII Ehlers-Danlos syndrome", "Ehlers-Danlos syndrome, type VIII", "EHLERS-DANLOS SYNDROME, TYPE VIII", "Ehlers-Danlos Syndrome, Type VIII", "periodontal Ehlers-Danlos syndrome", "Periodontal Ehlers-Danlos syndrome", "Ehlers-Danlos syndrome type 8 (formerly)", "Ehlers-Danlos syndrome, type 8 (disorder)", "Ehlers-Danlos Syndrome, Periodontosis Type", "EHLERS-DANLOS SYNDROME, PERIODONTOSIS TYPE", "Ehlers-Danlos Syndrome, Periodontitis Type", "Ehlers-Danlos syndrome, periodontosis type", "Ehlers-Danlos syndrome, periodontitis type", "EHLERS-DANLOS SYNDROME, PERIODONTITIS TYPE", "Ehlers-Danlos syndrome, type VIII (formerly)", "Ehlers-Danlos syndrome, type VIII (diagnosis)", "Periodontitis associated with Ehlers-Danlos syndrome type VIII"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ehlers-Danlos syndrome, periodontitis type", "shortest_name_length": 4}
{"curie": "MONDO:0011566", "names": ["AOMS2", "Aoms2", "Abdominal obesity-metabolic syndrome", "ABDOMINAL OBESITY-METABOLIC SYNDROME QUANTITATIVE TRAIT LOCUS 2", "abdominal obesity-metabolic syndrome quantitative trait locus 2", "abdominal obesity-metabolic syndrome quantitative trait locus type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "abdominal obesity-metabolic syndrome quantitative trait locus 2", "shortest_name_length": 5}
{"curie": "MONDO:0009618", "names": ["MICROCEPHALY-CARDIOMYOPATHY", "microcephaly-cardiomyopathy", "Microcephaly-Cardiomyopathy", "Microcephaly cardiomyopathy", "Winship Viljoen Leary syndrome", "Winship-Viljoen-Leary syndrome", "microcephaly with cardiomyopathy", "Microcephaly with cardiomyopathy", "Microcephaly cardiomyopathy syndrome", "Microcephaly-cardiomyopathy syndrome", "microcephaly-cardiomyopathy syndrome", "microcephalus cardiomyopathy syndrome", "Microcephalus cardiomyopathy syndrome", "Microcephalus cardiomyopathy syndrome (disorder)", "microcephalus cardiomyopathy syndrome (diagnosis)", "severe microcephaly and self-limiting dilated cardiomyopathy", "Severe microcephaly and self-limiting dilated cardiomyopathy", "Microcephaly with mental retardation and dilated cardiomyopathy", "multiple malformation syndrome microcephalus cardiomyopathy syndrome", "Severe microcephaly with mental retardation and dilated cardiomyopathy", "severe microcephaly with mental retardation and dilated cardiomyopathy", "severe microcephaly with intellectual disability and dilated cardiomyopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly-cardiomyopathy syndrome", "shortest_name_length": 27}
{"curie": "MONDO:0010062", "names": ["spinocerebellar ataxia with dysmorphism", "SPINOCEREBELLAR ATAXIA WITH DYSMORPHISM", "Spinocerebellar Ataxia with Dysmorphism", "spinocerebellar ataxia-dysmorphism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia-dysmorphism syndrome", "shortest_name_length": 39}
{"curie": "MONDO:0008304", "names": ["PCS", "premature chromatid separation trait", "PREMATURE CHROMATID SEPARATION TRAIT", "total premature chromatid separation trait", "TOTAL PREMATURE CHROMATID SEPARATION TRAIT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "premature chromatid separation trait", "shortest_name_length": 3}
{"curie": "UMLS:C5206745", "names": ["Recurrent Systemic Anaplastic Large Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Systemic Anaplastic Large Cell Lymphoma", "shortest_name_length": 49}
{"curie": "MESH:D014545", "names": ["Urinary Calculi"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urinary Calculi", "shortest_name_length": 15}
{"curie": "MONDO:0100462", "names": ["OD", "SSOAOD", "Familial Osteochondritis Dissecans", "Familial osteochondritis dissecans", "osteochondritis dissecans and short stature", "Osteochondritis dissecans and short stature", "Familial osteochondritis dissecans (disorder)", "Osteochondritis Dissecans, Short Stature, and Early-Onset Osteoarthritis", "OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS", "osteochondritis dissecans, short stature, and early-onset osteoarthritis", "short stature and advanced bone age, with or without early-onset osteoarthritis and/or osteochondritis dissecans", "SHORT STATURE AND ADVANCED BONE AGE, WITH OR WITHOUT EARLY-ONSET OSTEOARTHRITIS AND/OR OSTEOCHONDRITIS DISSECANS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short stature and advanced bone age, with or without early-onset osteoarthritis and/or osteochondritis dissecans", "shortest_name_length": 2}
{"curie": "MONDO:0005722", "names": ["Croup", "CROUP", "croup", "croup syndrome", "Croup syndrome", "croup syndromes", "Croup (disorder)", "croup (diagnosis)", "Laryngotracheitis", "acute laryngotracheitis", "Laryngotracheobronchitis", "acute Obstructive Laryngitis", "acute obstructive laryngitis", "Acute Obstructive Laryngitis", "Acute laryngotracheobronchitis", "acute laryngotracheobronchitis", "acute; laryngotracheobronchitis", "laryngotracheobronchitis; acute", "LARYNGOTRACHEOBRONCHITIS, ACUTE", "Acute obstructive laryngitis [croup]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "croup", "shortest_name_length": 5}
{"curie": "MONDO:0700012", "names": ["chromosome 5 disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 5 disorder", "shortest_name_length": 21}
{"curie": "UMLS:C1332304", "names": ["Anterior Tongue Carcinoma", "Carcinoma of Anterior Tongue", "Carcinoma of the Anterior Tongue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anterior Tongue Carcinoma", "shortest_name_length": 25}
{"curie": "UMLS:C4727176", "names": ["Refractory EBV-Positive Diffuse Large B-Cell Lymphoma, NOS", "Refractory EBV-Positive Diffuse Large B-Cell Lymphoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory EBV-Positive Diffuse Large B-Cell Lymphoma, Not Otherwise Specified", "shortest_name_length": 58}
{"curie": "MONDO:0000811", "names": ["BWGS", "ALCAPA", "ALCAPA disorder", "ALCAPA Syndrome", "Syndrome, ALCAPA", "ALCAPA Syndromes", "White-Garland syndrome", "Bland-White-Garland syndrome", "Bland White Garland Syndrome", "Bland-White-Garland Syndrome", "Bland-Garland-White syndrome", "Syndrome, Bland-White-Garland", "anomalous left coronary artery from the pulmonary artery", "Anomalous left coronary artery from the pulmonary artery", "Anomalous origin of left coronary artery from pulmonary artery", "Anomalous origin of left coronary artery from the pulmonary artery", "Anomalous origin of left coronary artery from pulmonary artery (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anomalous left coronary artery from the pulmonary artery", "shortest_name_length": 4}
{"curie": "MONDO:0010933", "names": ["DVA", "DFNB4", "NSRD4", "DILATED VESTIBULAR AQUEDUCT", "dilated vestibular aqueduct", "Widened vestibular aqueduct", "Dilated Vestibular Aqueduct", "Dilated vestibular aqueduct", "Enlarged Vestibular Aqueduct", "Enlarged vestibular aqueduct", "enlarged vestibular aqueduct", "Deafness, Autosomal Recessive 4", "enlarged vestibular aqueduct, digenic", "autosomal recessive nonsyndromic deafness 4", "neurosensory nonsyndromic recessive deafness 4", "NEUROSENSORY NONSYNDROMIC RECESSIVE DEAFNESS 4", "Neurosensory Nonsyndromic Recessive Deafness 4", "autosomal recessive nonsyndromic hearing loss 4", "autosomal recessive nonsyndromic deafness type 4", "autosomal recessive deafness 4 with enlarged vestibular aqueduct", "Autosomal Recessive Deafness-4 with Enlarged Vestibular Aqueduct", "deafness, autosomal recessive 4, with enlarged vestibular aqueduct", "Deafness, Autosomal Recessive 4, with Enlarged Vestibular Aqueduct", "DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 4", "shortest_name_length": 3}
{"curie": "UMLS:C0347629", "names": ["Esophageal laceration", "Oesophageal laceration", "laceration of esophagus", "Laceration of esophagus", "Laceration Of Esophagus", "Laceration of oesophagus", "Laceration(s) of Esophagus", "Laceration of esophagus (disorder)", "laceration of esophagus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laceration of esophagus", "shortest_name_length": 21}
{"curie": "MONDO:0017428", "names": ["congenital deformities of fingers"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital deformities of fingers", "shortest_name_length": 33}
{"curie": "MONDO:0009794", "names": ["OFD4", "Ofds 4", "OFDS IV", "OFD syndrome 4", "Mohr Majewski syndrome", "MOHR-MAJEWSKI SYNDROME", "Mohr-Majewski syndrome", "Baraitser Burn syndrome", "Baraitser-Burn syndrome", "BARAITSER-BURN SYNDROME", "orofaciodigital syndrome 4", "Orofaciodigital syndrome 4", "orofaciodigital syndrome IV", "Orofaciodigital Syndrome IV", "OROFACIODIGITAL SYNDROME IV", "digito-orofacial syndrome IV", "Orofacial-digital syndrome IV", "oral facial digital syndrome 4", "Orofaciodigital syndrome type 4", "oral-facial-digital syndrome IV", "orofaciodigital syndrome type 4", "Ofd syndrome with tibial defects", "orofaciodigital syndrome type IV", "OFD SYNDROME WITH TIBIAL DEFECTS", "OFD Syndrome With Tibial Defects", "OFD Syndrome, Baraitser-Burn Type", "orofaciodigital (OFD) syndrome IV", "Ofd syndrome, Baraitser-Burn type", "OFD SYNDROME, BARAITSER-BURN TYPE", "Oral-facial-digital syndrome type 4", "oral facial digital syndrome type 4", "oral-facial-digital syndrome type 4", "oral-Facial-digital syndrome, type 4", "Oral Facial Digital Syndrome, Type IV", "ORAL-FACIAL-DIGITAL SYNDROME, TYPE IV", "OFD IV - Orofacial-digital syndrome IV", "Orofacial-digital syndrome IV (disorder)", "orofaciodigital syndrome with tibial dysplasia", "Orofaciodigital syndrome with tibial dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orofaciodigital syndrome IV", "shortest_name_length": 4}
{"curie": "MONDO:0003968", "names": ["asynchronous multifocal osteosarcoma", "Asynchronous Multifocal Osteosarcoma", "asynchronous multifocal osteogenic sarcoma", "Asynchronous Multifocal Osteogenic Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "asynchronous multifocal osteogenic sarcoma", "shortest_name_length": 36}
{"curie": "MONDO:0009059", "names": ["CYSTEINE PEPTIDURIA", "Cysteine Peptiduria", "cysteine Peptiduria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cysteine Peptiduria", "shortest_name_length": 19}
{"curie": "MONDO:0017816", "names": ["amyloidosis systemic", "systemic amyloidosis", "Systemic amyloidosis", "Amyloidosis Systemic", "systemic; amyloidosis", "amyloidosis; systemic", "Systemic AL amyloidosis", "systemic AL amyloidosis", "Systemic amyloidosis, NOS", "primary systemic amyloidosis", "Primary systemic amyloidosis", "Primary Systemic Amyloidosis", "systemic amyloidosis, primary", "amyloidosis, primary systemic", "Systemic amyloidosis (disorder)", "systemic amyloidosis (diagnosis)", "systemic immunoglobulin light chain amyloidosis", "systemic Immunoglobulin Light chain amyloidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary systemic amyloidosis", "shortest_name_length": 20}
{"curie": "MONDO:0004432", "names": ["Mature Pericardial Teratoma", "benign pericardial teratoma", "pericardium mature teratoma", "mature pericardial teratoma", "Pericardial Mature Teratoma", "mature teratoma of pericardium", "Mature Teratoma of Pericardium", "Mature teratoma of Pericardium", "Mature Teratoma of the Pericardium", "mature teratoma of the pericardium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mature pericardial teratoma", "shortest_name_length": 27}
{"curie": "UMLS:C4727282", "names": ["Locally Advanced Unresectable Bone Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Unresectable Bone Sarcoma", "shortest_name_length": 42}
{"curie": "MONDO:0002489", "names": ["phyllodes breast tumor", "phyllodes breast tumour", "phyllodes breast neoplasm", "malignant phyllodes tumor", "Phyllodes breast neoplasm", "malignant phyllodes tumour", "Phyllodes tumor, malignant", "malignant Phyllodes neoplasm", "malignant phyllodes neoplasm", "breast malignant phyllodes tumor", "Malignant Breast Phyllodes Tumor", "malignant breast phyllodes tumor", "malignant cystosarcoma phyllodes", "breast phyllodes tumor, malignant", "breast malignant phyllodes tumour", "malignant Mammary Phyllodes tumor", "malignant mammary phyllodes tumor", "Malignant Mammary Phyllodes Tumor", "malignant Mammary Phyllodes tumour", "Malignant Breast Phyllodes Neoplasm", "malignant breast phyllodes neoplasm", "Malignant Phyllodes Breast Neoplasm", "malignant phyllodes tumor of breast", "Malignant phyllodes tumor of breast", "Malignant Phyllodes Tumor of Breast", "malignant phyllodes breast neoplasm", "Malignant Mammary Phyllodes Neoplasm", "malignant phyllodes tumour of breast", "malignant mammary phyllodes neoplasm", "Malignant phyllodes tumour of breast", "malignant phyllodes neoplasm of breast", "Malignant Phyllodes Neoplasm of Breast", "malignant phyllodes tumor of the breast", "Malignant Phyllodes Tumor of the Breast", "Malignant cystosarcoma phyllodes of breast", "malignant phyllodes neoplasm of the breast", "malignant cystosarcoma phyllodes of breast", "Malignant Phyllodes Neoplasm of the Breast", "malignant cystosarcoma phyllodes of the breast", "Malignant phyllodes tumor of breast (disorder)", "malignant phyllodes tumor of breast (diagnosis)", "malignant phyllodes tumor (morphologic abnormality)", "phyllodes tumor, malignant (morphologic abnormality)", "malignant cystosarcoma phyllodes (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant breast phyllodes tumor", "shortest_name_length": 22}
{"curie": "MONDO:0005210", "names": ["Uterus Sarcoma", "Sarcoma uterus", "uterus sarcoma", "sarcoma uterus", "uterine sarcoma", "Uterine Sarcoma", "Uterine sarcoma", "sarcoma uterine", "UTERINE SARCOMA", "sarcomas uterine", "Sarcoma of Uterus", "sarcoma of uterus", "Sarcoma of uterus", "Uterine sarcoma NOS", "uterine body sarcoma", "Corpus Uteri Sarcoma", "corpus uteri sarcoma", "Uterine Body Sarcoma", "Sarcoma of the Uterus", "sarcoma of the uterus", "Body of Uterus Sarcoma", "body of uterus sarcoma", "Uterine Corpus Sarcoma", "uterus cancer, sarcoma", "uterine sarcoma cancer", "uterine corpus sarcoma", "uterine cancer sarcoma", "sarcoma of corpus uteri", "sarcoma of Corpus Uteri", "sarcoma of uterine body", "Sarcoma of corpus uteri", "Sarcoma of Corpus Uteri", "Sarcoma of Uterine Body", "uterine cancer, sarcoma", "Sarcoma of body of uterus", "Sarcoma of Body of Uterus", "Sarcoma of Uterine Corpus", "sarcoma of body of uterus", "sarcoma of uterine corpus", "Sarcoma of the Corpus Uteri", "Sarcoma of the Uterine Body", "sarcoma of the corpus uteri", "uterine sarcoma/mesenchymal", "sarcoma of the uterine body", "Sarcoma of the corpus uteri", "Sarcoma of uterus (disorder)", "sarcoma of the uterine corpus", "Sarcoma of the Body of Uterus", "sarcoma of uterus (diagnosis)", "sarcoma of the body of uterus", "Sarcoma of the Uterine Corpus", "uterine corpus cancer, sarcoma", "Sarcoma of body of uterus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine corpus sarcoma", "shortest_name_length": 14}
{"curie": "MONDO:0010378", "names": ["AUNX1", "DFNX5", "X-linked deafness 5", "Deafness, X-Linked 5", "DEAFNESS, X-LINKED 5", "deafness, X-linked 5", "X-linked HSAN with deafness", "DEAFNESS, X-LINKED 5 (disorder)", "X-linked HSAN with hearing loss", "deafness, X-linked 5, X-linked recessive", "X-Linked Deafness-5, with Peripheral Neuropathy", "DEAFNESS, X-LINKED 5, WITH PERIPHERAL NEUROPATHY", "X-linked auditory neuropathy 1 with peripheral sensory neuropathy", "X-linked hereditary sensory and autonomic neuropathy with deafness", "Auditory Neuropathy, X-Linked, 1, with Peripheral Sensory Neuropathy", "auditory neuropathy, X-linked, 1, with peripheral sensory neuropathy", "AUDITORY NEUROPATHY, X-LINKED, 1, WITH PERIPHERAL SENSORY NEUROPATHY", "X-linked hereditary sensory and autonomic neuropathy with hearing loss", "X-linked auditory neuropathy with peripheral sensory neuropathy type 1", "X-linked HSAN (hereditary sensory and autonomic neuropathy) with deafness", "X-linked hereditary sensory and autonomic neuropathy with deafness (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked hereditary sensory and autonomic neuropathy with hearing loss", "shortest_name_length": 5}
{"curie": "UMLS:C5235953", "names": ["Locally Advanced Ewing Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Ewing Sarcoma", "shortest_name_length": 30}
{"curie": "UMLS:C1707385", "names": ["chlamydia mucosa-associated lymphoid tissue (MALT) lymphoma of the ocular adnexae", "Chlamydia psittaci-Associated Ocular Adnexal Mucosa-Associated Lymphoid Tissue Lymphoma", "Chlamydia Psittaci-Associated Ocular Adnexal Mucosa-Associated Lymphoid Tissue Lymphoma", "Chlamydophila Psittaci-Associated Ocular Adnexal Mucosa-Associated Lymphoid Tissue Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chlamydia Psittaci-Associated Ocular Adnexal Mucosa-Associated Lymphoid Tissue Lymphoma", "shortest_name_length": 81}
{"curie": "UMLS:C3899976", "names": ["BCLC Stage D Hepatocellular Cancer", "BCLC Stage D Adult Hepatocellular Carcinoma", "Barcelona Clinic Liver Cancer Stage D Adult Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "BCLC Stage D Adult Hepatocellular Carcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0000265", "names": ["Mendelson", "Mendelson Syndrome", "Mendelson syndrome", "Syndrome, Mendelson", "Mendelsons Syndrome", "Mendelsons syndrome", "syndrome, Mendelson", "PNEUMONIA ASPIRATION", "Aspiration pneumonia", "Mendelson's syndrome", "ASPIRATION PNEUMONIA", "inhalation pneumonia", "aspiration pneumonia", "Inhalation pneumonia", "Mendelson's Syndrome", "Pneumonia aspiration", "Aspiration Pneumonia", "Pneumonia;aspiration", "pneumonia aspiration", "pneumonia; aspiration", "aspiration Pneumonias", "ASPIRATION PNEUMONIAS", "Pneumonia, Aspiration", "Syndrome, Mendelson's", "Aspiration Pneumonias", "Pneumonia, inhalation", "Pneumonia, aspiration", "PNEUMONIA, ASPIRATION", "syndrome, Mendelson's", "pneumonia, inhalation", "Aspiration pneumonitis", "Inhalational pneumonia", "Pneumonias, aspiration", "Pneumonias, Aspiration", "aspiration pneumonitis", "acid aspiration syndrome", "Aspiration pneumonia NOS", "Acid Aspiration Syndrome", "Acid Aspiration Syndromes", "acid aspiration syndromes", "syndrome, acid aspiration", "Syndrome, Acid Aspiration", "Aspiration pneumonia, NOS", "Syndromes, Acid Aspiration", "syndromes, acid aspiration", "Aspiration pneumonitis, NOS", "aspiration pneumonia (disease)", "Aspiration pneumonia (disorder)", "Mendelson's syndrome (diagnosis)", "aspiration pneumonia (diagnosis)", "Gastric Acid Aspiration Syndrome", "gastric acid aspiration syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aspiration pneumonia", "shortest_name_length": 9}
{"curie": "OMIM:223200", "names": ["DS", "DISORGANIZATION, MOUSE, HOMOLOG OF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 2}
{"curie": "UMLS:C5552729", "names": ["Recurrent Indolent Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Indolent Non-Hodgkin Lymphoma", "shortest_name_length": 39}
{"curie": "UMLS:C5555671", "names": ["Metastatic Digestive System Neuroendocrine Tumor G2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Digestive System Neuroendocrine Tumor G2", "shortest_name_length": 51}
{"curie": "UMLS:C1265603", "names": ["Firm Mass", "Firm mass", "Firm mass (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Firm mass", "shortest_name_length": 9}
{"curie": "MONDO:0016924", "names": ["Duplication of chromosome 4", "partial trisomy of chromosome 4", "Partial trisomy of chromosome 4", "Partial duplication of chromosome 4", "partial duplication of chromosome 4", "partial duplication of chromosome type 4", "Partial trisomy of chromosome 4 (disorder)", "Partial trisomy of chromosome 4 (diagnosis)", "anomaly of chromosome pair 4 partial trisomy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of chromosome 4", "shortest_name_length": 27}
{"curie": "MONDO:0015300", "names": ["Cataract microcornea syndrome", "cataract microcornea syndrome", "Cataract-microcornea syndrome", "microcornea cataract syndrome", "Microcornea cataract syndrome", "Microcornea-Cataract Syndrome", "Cataract-Microcornea Syndrome", "cataract - microcornea syndrome", "Cataract and microcornea syndrome", "Cataract and microcornea syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract - microcornea syndrome", "shortest_name_length": 29}
{"curie": "UMLS:C4087263", "names": ["persistent depressive disorder", "Persistent depressive disorder", "Persistent depressive disorder (disorder)", "persistent depressive disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Persistent depressive disorder", "shortest_name_length": 30}
{"curie": "MONDO:0019195", "names": ["IBM3", "HIBM3", "Inclusion body myopathy type 3", "inclusion body myopathy type 3", "Hereditary inclusion body myopathy type 3", "hereditary inclusion body myopathy type 3", "Inclusion body myopathy autosomal dominant", "Hereditary inclusion body myopathy - joint contractures - ophthalmoplegia", "Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome", "hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome", "Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome", "Myopathy with congenital joint contractures, ophthalmoplegia, and rimmed vacuoles", "Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0019000", "names": ["Tarlov Cyst", "tarlov cyst", "Tarlov cyst", "cyst tarlov", "cyst tarlovs", "cysts tarlov", "Tarlov cysts", "tarlov cysts", "Cyst, Tarlov", "Tarlov Cysts", "Cysts, Tarlov", "tarlov's cyst", "Tarlov's cyst", "cysts tarlov's", "nerve root cyst", "root nerve cyst", "Perineural cyst", "cyst nerve root", "Nerve root cyst", "perineural cyst", "Perineural Cyst", "Nerve Root Cyst", "cysts perineural", "perineurial cyst", "perineural cysts", "cysts nerve root", "Perineurial Cyst", "Perineural Cysts", "Cyst, Perineural", "Perineurial cyst", "Cysts, Perineural", "Perineurial Cysts", "cysts perineurial", "Cyst, Perineurial", "Cysts, Perineurial", "Cyst of Nerve Root", "Sacral Tarlov Cysts", "sacral neural cysts", "sacral Tarlov cysts", "Cysts, Sacral Tarlov", "Sacral Perineural Cyst", "Cyst of the Nerve Root", "Cyst, Sacral Perineural", "Tarlov cyst (diagnosis)", "sacral perineural cysts", "Sacral Perineural Cysts", "Cysts, Sacral Perineural", "Perineural cyst (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "perineural cyst", "shortest_name_length": 11}
{"curie": "MONDO:0005136", "names": ["Malaria", "malaria", "MALARIA", "Paludism", "malarias", "paludism", "Marsh Fever", "marsh fever", "Malaria NOS", "Malaria, NOS", "Fever, Marsh", "plasmodiosis", "Plasmodiosis", "jungle; fever", "fever malaria", "malaria fever", "fever; jungle", "malarial fever", "Cameroon fever", "fever; paludal", "Corsican fever", "Malarial fever", "paludal; fever", "fever; corsican", "Remittent Fever", "Cameroon; fever", "fever; Cameroon", "induced malaria", "corsican; fever", "Fever, Remittent", "Malaria fever NOS", "Malaria (disorder)", "fever; jungle fever", "malaria (diagnosis)", "Unspecified malaria", "jungle fever; fever", "Plasmodium Infection", "Malaria, unspecified", "Plasmodia infections", "Plasmodium infection", "Plasmodium Infections", "Infection, Plasmodium", "Infections, Plasmodium", "Malarial fever (finding)", "Disease due to Plasmodiidae", "DISEASES DUE TO PLASMODIIDAE", "Disease caused by Plasmodiidae", "malarial fever (physical finding)", "Disease caused by Plasmodiidae (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malaria", "shortest_name_length": 7}
{"curie": "MONDO:0010232", "names": ["IPOX", "Ipox", "CIIP", "CIIPX", "CIIP X-linked", "CIIP, X-LINKED", "Ciip, X-linked", "CONGENITAL SHORT BOWEL SYNDROME, X-LINKED", "congenital short bowel syndrome, X-linked", "Intestinal pseudoobstruction chronic idiopathic", "Congenital idiopathic intestinal pseudoobstruction", "congenital idiopathic intestinal pseudoobstruction", "CONGENITAL IDIOPATHIC INTESTINAL PSEUDOOBSTRUCTION", "congenital short bowel syndrome, X-linked recessive", "X-linked chronic idiopathic intestinal pseudo-obstruction", "intestinal pseudoobstruction, neuronal, X-linked recessive", "intestinal pseudoobstruction neuronal chronic idiopathic X-linked", "INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED", "Intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked", "intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked", "INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, WITH CENTRAL NERVOUS SYSTEM INVOLVEMENT", "Intestinal Pseudoobstruction, Neuronal, Chronic Idiopathic, with Central Nervous System Involvement", "intestinal pseudoobstruction, neuronal, chronic idiopathic, with central nervous system involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked", "shortest_name_length": 4}
{"curie": "UMLS:C4744561", "names": ["Metastatic Lung Adenosquamous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Lung Adenosquamous Carcinoma", "shortest_name_length": 39}
{"curie": "UMLS:C0264956", "names": ["atheroma", "Atheroma", "atheromas", "Atheromas", "atheromatous", "Atheromatous", "Atheroma, NOS", "Atheroma of artery", "atheroma of artery", "atheromatous plaque", "Atheromatous Plaque", "Atheromatous plaque", "Atheromatous Plaques", "Plaque, Atheromatous", "Atheroma of artery, NOS", "Atheromatous plaque, NOS", "Atheromatous degeneration", "Atheroma of artery (disorder)", "atheroma of artery (diagnosis)", "Atheroma (morphologic abnormality)", "Atheromatous degeneration (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atheroma", "shortest_name_length": 8}
{"curie": "UMLS:C0274714", "names": ["Adrenergic syndrome", "Adrenergic poisoning", "Poisoning by adrenergics", "sympathomimetic toxicity", "Sympathomimetic poisoning", "Poisoning by adrenergic drug", "Poisoning by sympathomimetics", "Poisoning by sympathomimetic drug", "Poisoning by adrenergic drug, NOS", "Poisoning caused by adrenergic drug", "sympathomimetic toxicity (diagnosis)", "Poisoning by sympathomimetic drug, NOS", "Poisoning caused by sympathomimetic drug", "Poisoning by sympathomimetics (adrenergics)", "Poisoning by sympathomimetics [adrenergics]", "Poisoning caused by sympathomimetic drug (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Poisoning by sympathomimetic drug", "shortest_name_length": 19}
{"curie": "UMLS:C2930617", "names": ["Pulmonary Fibrosis - from Asbestos Exposure", "Idiopathic Interstitial Pneumonitis - from Asbestos Exposure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pulmonary Fibrosis - from Asbestos Exposure", "shortest_name_length": 43}
{"curie": "UMLS:C0236101", "names": ["Neonatal and infancy disorder", "Neonatal and Infancy Disorders", "NEONATAL AND INFANCY DISORDERS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neonatal and infancy disorder", "shortest_name_length": 29}
{"curie": "MONDO:0009000", "names": ["RPC", "familial reactive perforating collagenosis", "Familial reactive perforating collagenosis", "Collagenosis, Familial Reactive Perforating", "collagenosis, familial reactive perforating", "inherited reactive perforating collagenosis", "COLLAGENOSIS, FAMILIAL REACTIVE PERFORATING"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial reactive perforating collagenosis", "shortest_name_length": 3}
{"curie": "MONDO:0000376", "names": ["respiratory system cancer", "Cancer of respiratory system", "cancer of respiratory system", "Malignant respiratory tract neoplasm", "Malignant Respiratory Tract Neoplasm", "Malignant Respiratory System Neoplasm", "malignant respiratory system neoplasm", "malignant neoplasm respiratory system", "Malignant neoplasm of respiratory system", "malignant neoplasm of respiratory system", "Malignant respiratory tract neoplasm NOS", "Malignant neoplasm of respiratory tract NOS", "Malignant neoplasm of respiratory tract, NOS", "Malignant neoplasm of respiratory system (disorder)", "malignant neoplasm of respiratory system (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "respiratory system cancer", "shortest_name_length": 25}
{"curie": "UMLS:C1707549", "names": ["Cutaneous Lymphomatoid Granulomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous Lymphomatoid Granulomatosis", "shortest_name_length": 37}
{"curie": "UMLS:C0009044", "names": ["WRIST FRACTURE CLOSED", "Closed fracture of wrist, NOS", "Closed fracture of carpal bone", "closed fracture of carpal bone", "Closed Fracture of Carpal Bone", "Closed fracture carpal bone, NOS", "Closed fractures of carpal bones", "Closed fracture of carpal bone of wrist", "Closed fracture of carpal bone (disorder)", "closed fracture of carpal bone (diagnosis)", "Closed fracture of carpal bone, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Closed fracture of carpal bone", "shortest_name_length": 21}
{"curie": "UMLS:C2985448", "names": ["Radiation-Related Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radiation-Related Sarcoma", "shortest_name_length": 25}
{"curie": "MONDO:0005412", "names": ["du", "Curling", "Stress Ulcer", "stress Ulcer", "curling ulcer", "curling Ulcer", "Curling Ulcer", "curlings ulcer", "Ulcer duodenal", "Ulcer;duodenal", "curling ulcers", "Duodenal Ulcer", "Duodenal ulcer", "Ulcer, Curling", "duodenal ulcer", "ULCER DUODENAL", "DUODENAL ULCER", "Curlings Ulcer", "Curling ulcers", "duodenum ulcer", "ULCER, CURLINGS", "Ulcer, Duodenal", "ulcer; duodenum", "curling's ulcer", "Duodenal Ulcers", "Curling's Ulcer", "Duodenal ulcers", "duodenal ulcers", "curlings ulcers", "duodenum ulcers", "Curling's ulcer", "duodenum; ulcer", "DUODENUM, ULCER", "Curling's ulcers", "Ulcers, Duodenal", "curling's ulcers", "Ulcer, Curling's", "Duodenum--Ulcers", "Ulcer of duodenum", "DUODENAL ULCERATION", "duodenal ulceration", "DU - Duodenal ulcer", "Duodenal ulcer, NOS", "Duodenal ulcer disease", "DUODENUM, PEPTIC ULCER", "DUODENAL ULCER DISEASE", "duodenum ulcer (peptic)", "Peptic ulcer of duodenum", "duodenal ulcer (disease)", "Duodenal ulcer (diagnosis)", "Curling's ulcer (disorder)", "Common duodenal ulcer, NOS", "duodenal ulcer (diagnosis)", "Duodenal ulcer disease, NOS", "DUD - Duodenal ulcer disease", "Ulcer of duodenum (disorder)", "Peptic ulcer of duodenum, NOS", "ULCER, GASTROINTESTINAL, FOLLOWING BURN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "duodenal ulcer", "shortest_name_length": 2}
{"curie": "MONDO:0032605", "names": ["MRT66", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 66", "intellectual disability, autosomal recessive 66", "autosomal recessive intellectual developmental disorder 66", "intellectual developmental disorder, autosomal recessive 66", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 66"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 66", "shortest_name_length": 5}
{"curie": "UMLS:C5418781", "names": ["Superficial Bladder Urothelial Carcinoma", "Superficial Bladder Transitional Cell Carcinoma", "Non-Muscle Invasive Bladder Urothelial Carcinoma", "Non-Muscle Invasive Bladder Transitional Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Muscle Invasive Bladder Urothelial Carcinoma", "shortest_name_length": 40}
{"curie": "UMLS:C4054536", "names": ["THSD7A Induced Membranous Nephropathy", "Membranous Nephropathy - THSD7A Induced", "Thrombospondin Type-1 domain-containing Protein Membranous Nephropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Membranous Nephropathy - THSD7A Induced", "shortest_name_length": 37}
{"curie": "MONDO:0013388", "names": ["DEE11", "EIEE11", "Early Infantile Epileptic Encephalopathy 11", "early infantile epileptic encephalopathy 11", "epileptic encephalopathy, early infantile, 11", "Developmental and Epileptic Encephalopathy 11", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 11", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11", "developmental and epileptic encephalopathy 11", "developmental and epileptic encephalopathy, 11", "SCN2A early infantile epileptic encephalopathy", "epileptic encephalopathy, early infantile, type 11", "early infantile epileptic encephalopathy caused by mutation in SCN2A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 11", "shortest_name_length": 5}
{"curie": "UMLS:C0000810", "names": ["Incomplete Abortion", "Incomplete Abortions", "Abortion, Incomplete", "Abortions, Incomplete", "Incomplete miscarriage", "Incomplete spontaneous abortion", "Abortion spontaneous incomplete", "incomplete spontaneous abortion", "Incomplete miscarriage (disorder)", "Retained products after miscarriage", "Abortion spontaneous incomplete NOS", "Retained tissue after pregnancy loss", "incomplete spontaneous abortion (diagnosis)", "Retained products after spontaneous abortion", "Retained products after miscarriage (disorder)", "Retained products after miscarriage (diagnosis)", "retained products of conception after miscarriage", "Retained products of conception following spontaneous termination of pregnancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Incomplete spontaneous abortion", "shortest_name_length": 19}
{"curie": "UMLS:C1334426", "names": ["Low Grade Accessory Sinus Sarcoma", "Low Grade Paranasal Sinus Sarcoma", "Low Grade Sarcoma of Accessory Sinus", "Low Grade Sarcoma of Paranasal Sinus", "Low Grade Sarcoma of the Paranasal Sinus", "Low Grade Sarcoma of the Accessory Sinus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Grade Paranasal Sinus Sarcoma", "shortest_name_length": 33}
{"curie": "MONDO:0006423", "names": ["Soft Tissue Chondroma", "Soft tissue chondroma", "soft tissue chondroma", "Extraskeletal Chondroma", "Chondroma of Soft Parts", "extraskeletal chondroma", "chondroma of soft parts", "Extraskeletal Osteochondroma", "extraskeletal osteochondroma", "Soft tissue chondroma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "soft tissue chondroma", "shortest_name_length": 21}
{"curie": "MONDO:0024607", "names": ["MDCCAID", "congenital muscular dystrophy with cataracts and intellectual disability", "muscular dystrophy, congenital, with cataracts and intellectual disability", "MUSCULAR DYSTROPHY, CONGENITAL, WITH CATARACTS AND INTELLECTUAL DISABILITY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital muscular dystrophy with cataracts and intellectual disability", "shortest_name_length": 7}
{"curie": "MONDO:0009533", "names": ["Dahlberg syndrome", "Dahlberg Borer Newcomer syndrome", "Dahlberg-Borer-Newcomer syndrome", "Lymphedema hypoparathyroidism syndrome", "Hypoparathyroidism Lymphedema syndrome", "Lymphedema-hypoparathyroidism syndrome", "lymphedema hypoparathyroidism syndrome", "Hypoparathyroidism-Lymphedema Syndrome", "lymphedema-hypoparathyroidism syndrome", "hypoparathyroidism-lymphedema syndrome", "LYMPHEDEMA-HYPOPARATHYROIDISM SYNDROME", "HYPOPARATHYROIDISM-LYMPHEDEMA SYNDROME", "hypoparathyroidism lymphedema syndrome", "Lymphedema-Hypoparathyroidism Syndrome", "Lymphoedema hypoparathyroidism syndrome", "Lymphedema hypoparathyroidism syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dahlberg-Borer-Newcomer syndrome", "shortest_name_length": 17}
{"curie": "MONDO:0008729", "names": ["CYP11B1 deficiency", "P450C11B1 deficiency", "P450C11B1 DEFICIENCY", "adrenal hyperplasia 4", "Adrenal hyperplasia 4", "ADRENAL HYPERPLASIA IV", "Adrenal Hyperplasia IV", "adrenal hyperplasia IV", "11B Hydroxylase Deficiency", "11b-hydroxylase deficiency", "CYP11B1 deficiency congenital", "congenital CYP11B1 deficiency", "11-Beta-hydroxylase deficiency", "11 beta-hydroxylase deficiency", "11 Beta Hydroxylase Deficiency", "11-BETA-HYDROXYLASE DEFICIENCY", "11-Beta-Hydroxylase Deficiency", "11-Beta-Hydroxylase deficiency", "11-beta-hydroxylase deficiency", "CAH - 11 beta-hydroxylase deficiency", "adrenal hyperplasia hypertensive form", "Congenital adrenal hyperplasia type 4", "STEROID 11-BETA-HYDROXYLASE DEFICIENCY", "Steroid 11 Beta Hydroxylase Deficiency", "ADRENAL HYPERPLASIA, HYPERTENSIVE FORM", "Steroid 11-Beta-Hydroxylase Deficiency", "steroid 11-Beta-Hydroxylase deficiency", "adrenal hyperplasia, hypertensive form", "Congenital adrenal hyperplasia, type 3", "Adrenal Hyperplasia, Hypertensive Form", "Steroid 11 beta-monooxygenase deficiency", "Hypertensive form of adrenal hyperplasia", "Steroid 11-beta-monooxygenase deficiency", "Deficiency of steroid 11-beta-hydroxylase", "CAH due to 11-beta-hydroxylase deficiency", "11-beta-hydroxylase deficiency (diagnosis)", "Deficiency of steroid 11-beta-monooxygenase", "Hypertensive congenital adrenal hyperplasia", "Deficiency of steroid 11-beta-monooxygenase (disorder)", "Adrenogenital disorder due to 11-beta-hydroxylase deficiency", "Adrenogenital disorder due to 11 beta-hydroxylase deficiency", "congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency", "Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency", "Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency", "Adrenal hyperplasia, congenital, due to 11-Beta-hydroxylase deficiency", "adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency", "adrenal hyperplasia, congenital, due to steroid 11-BETA-HYDROXYLASE deficiency", "ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASE DEFICIENCY", "Adrenal Hyperplasia, Congenital, Due To Steroid 11-Beta-Hydroxylase Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency", "shortest_name_length": 18}
{"curie": "MONDO:0022699", "names": ["cerebral palsy spastic hemiplegic", "spastic hemiplegia cerebral palsy", "spastic hemiplegic cerebral palsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral palsy spastic hemiplegic", "shortest_name_length": 33}
{"curie": "UMLS:C5670692", "names": ["AIDS-Related Diffuse Large B-Cell Lymphoma of the Central Nervous System", "AIDS-Associated Diffuse Large B-Cell Lymphoma of the Central Nervous System", "AIDS-Related Primary Diffuse Large B-Cell Lymphoma of the Central Nervous System", "AIDS-Associated Primary Diffuse Large B-Cell Lymphoma of the Central Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Primary Diffuse Large B-Cell Lymphoma of the Central Nervous System", "shortest_name_length": 72}
{"curie": "UMLS:C4682559", "names": ["Stage III Uterine Corpus Leiomyosarcoma", "Stage III Uterine Corpus Leiomyosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Uterine Corpus Leiomyosarcoma AJCC v8", "shortest_name_length": 39}
{"curie": "UMLS:C0588008", "names": ["Severe depression", "depression severe", "severe depression", "severe; depression", "depression; severe", "Severe depression (disorder)", "Severe depression (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Severe depression", "shortest_name_length": 17}
{"curie": "MONDO:0015555", "names": ["plaque-form urticaria pigmentosa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "plaque-form urticaria pigmentosa", "shortest_name_length": 32}
{"curie": "UMLS:C1369136", "names": ["Anal cancer metastatic", "metastatic anus cancer", "metastatic anal cancer", "Metastatic Anal Cancer", "anus cancer, metastatic", "anal cancer, metastatic", "Metastatic Anal Carcinoma", "Secondary Cancer from the Anus", "Metastatic Anal Canal Carcinoma", "Metastatic Cancer from the Anus", "Secondary Carcinoma from the Anus", "Metastatic Carcinoma from the Anus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Anal Canal Carcinoma", "shortest_name_length": 22}
{"curie": "MONDO:0001912", "names": ["Acute frontal sinusitis", "acute frontal sinusitis", "frontal sinusitis, acute", "sinusitis; frontalis, acute", "sinusitis; acute, frontalis", "sinusitis; frontal sinus, acute", "sinusitis; acute, frontal sinus", "Acute frontal sinusitis (disorder)", "acute frontal sinusitis (diagnosis)", "Acute frontal sinusitis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute frontal sinusitis", "shortest_name_length": 23}
{"curie": "UMLS:C0546343", "names": ["Mucosal erosion", "Mucosal erosion NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mucosal erosion", "shortest_name_length": 15}
{"curie": "MONDO:0005746", "names": ["Pinworm", "pinworms", "Pinworms", "Oxyuriases", "OXYURIASIS", "Oxyuriasis", "THREADWORM", "oxyuriasis", "threadworms", "Threadworms", "ENTEROBIASIS", "Enterobiases", "Enterobiasis", "enterobiasis", "Enterobiosis", "pinworm disease", "Pinworm disease", "pinworm; disease", "pinworm infection", "Pinworm Infection", "Pinworm infection", "Seatworm infection", "Pinworm Infections", "INFECTION, PINWORM", "Infection, Pinworm", "Pinworm infestation", "Infections, Pinworm", "INFECTION, SEATWORM", "threadworm infection", "Threadworm Infection", "Threadworm infection", "threadworm; infection", "Infection with Oxyuris", "Enterobiasis threadworm", "Enterobiasis (disorder)", "enterobiasis (diagnosis)", "Enterobiasis - threadworm", "Pinworm infection (disorder)", "Oxyuris vermicularis infection", "Oxyuris vermicularis Infection", "disease (or disorder); pinworm", "Oxyuris vermicularis Infections", "Infection, Oxyuris vermicularis", "Infections, Oxyuris vermicularis", "Oxyuris vermicularis; infestation", "Infection with Oxyuris (disorder)", "infestation; Oxyuris vermicularis", "Enterobius vermicularis Infection", "Enterobius vermicularis infection", "Enterobius vermicularis Infections", "Infection, Enterobius vermicularis", "Infections, Enterobius vermicularis", "Enterobius vermicularis; infestation", "infestation; Enterobius vermicularis", "Infection by Enterobius vermicularis", "Enterobius vermicularis infectious disease", "Enterobius vermicularis disease or disorder", "Infection caused by Enterobius vermicularis", "Enterobius vermicularis caused disease or disorder", "Infection caused by Enterobius vermicularis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "enterobiasis", "shortest_name_length": 7}
{"curie": "MONDO:0009201", "names": ["FACIAL ABNORMALITIES, KYPHOSCOLIOSIS, AND MENTAL RETARDATION", "Facial Abnormalities, Kyphoscoliosis, and Mental Retardation", "facial abnormalities, kyphoscoliosis, and mental retardation", "facial abnormalities, kyphoscoliosis, and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "facial abnormalities, kyphoscoliosis, and intellectual disability", "shortest_name_length": 60}
{"curie": "MONDO:0020366", "names": ["GLC3", "BUPHTHALMOS", "BUPHTMALMOS", "buphthalmia", "Buphthalmia", "buphthalmos", "Buphthalmos", "Buphthalmus", "Hydrophthalmos", "hydrophthalmos", "Newborn glaucoma", "Buphthalmos, NOS", "Juvenile glaucoma", "Glaucoma, newborn", "glaucoma; newborn", "newborn; glaucoma", "Childhood glaucoma", "Pediatric glaucoma", "infantile glaucoma", "Infantile glaucoma", "Congenital glaucoma", "Glaucoma congenital", "infantile; glaucoma", "GLAUCOMA, INFANTILE", "Paediatric glaucoma", "congenital glaucoma", "Glaucoma of newborn", "glaucoma; infantile", "GLAUCOMA CONGENITAL", "Congenital Glaucoma", "GLAUCOMA, CONGENITAL", "Glaucoma, congenital", "glaucoma; congenital", "congenital; glaucoma", "Congenital glaucomas", "Glaucoma of childhood", "Developmental glaucoma", "Primary congenital glaucoma", "primary congenital glaucoma", "Congenital glaucoma (disorder)", "congenital glaucoma (diagnosis)", "Glaucoma, open angle, congenital"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital glaucoma", "shortest_name_length": 4}
{"curie": "MONDO:0009678", "names": ["FCMD", "MDDGA4", "Fukuyama CMD", "CMD, Fukuyama", "Fukuyama Syndrome", "Fukuyama syndrome", "Syndrome, Fukuyama", "Fukuyama Muscular Dystrophy", "fukuyama muscular dystrophy", "muscular dystrophy fukuyama", "Fukuyama muscular dystrophy", "Muscular Dystrophy, Fukuyama", "Dystrophy, Fukuyama Muscular", "muscle-eye-brain-FKTN related", "Fktn-Related Walker-Warburg Syndrome", "Syndrome, Fktn-Related Walker-Warburg", "Fktn-Related Walker-Warburg Syndromes", "Walker Warburg Syndrome, Fktn Related", "Walker-Warburg Syndrome, Fktn-Related", "micropolygyria with muscular dystrophy", "Fukuyama congenital muscular dystrophy", "FUKUYAMA CONGENITAL MUSCULAR DYSTROPHY", "Fukuyama Congenital Muscular Dystrophy", "Cerebromuscular Dystrophy, Fukuyama Type", "FKTN-related congenital muscular dystrophy", "Fukuyama Type Congenital Muscular Dystrophy", "Congenital muscular dystrophy, Fukuyama type", "congenital muscular dystrophy, Fukuyama type", "Fukuyama congenital muscular dystrophy (FCMD)", "Muscular Dystrophy, Congenital, Fukuyama Type", "Fukuyama congenital muscular dystrophy (disorder)", "WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, FKTN-RELATED", "Walker-Warburg syndrome or muscle-eye-brain disease, FKTN-related", "congenital progressive muscular dystrophy with mental retardation", "Muscular Dystrophy due to Defective Glycosylation of Dystroglycan 4A", "congenital muscular dystrophy with central nervous system involvement", "muscular dystrophy-dystroglycanopathy (congenital with Brain and eye anomalies) type A, 4", "Muscular Dystrophy-Dystroglycanopathy (Congenital with Brain and Eye Anomalies) Type A, 4", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4", "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4", "shortest_name_length": 4}
{"curie": "MONDO:0016471", "names": ["PC", "pachyonychia congenita", "Pachyonychia congenita", "Pachyonychia Congenita", "Congenital Pachyonychia", "Congenital pachyonychia", "congenital pachyonychia", "Pachyonychia, Congenital", "Pachyonychia Congenita Type 1", "pachyonychia congenita type 1", "Jadassohn-Lewandowsky Syndrome", "Jadassohn-Lewandowsky syndrome", "Pachyonychia congenita syndrome", "Pachyonychia Congenita Syndrome", "pachyonychia congenita syndrome", "congenital pachyonychia (diagnosis)", "Jackson-Lawler Type Pachyonychia Congenita", "Jackson-Lawler type pachyonychia congenita", "Pachyonychia congenita syndrome (disorder)", "PACHYONYCHIA CONGENITA, JADASSOHN-LEWANDOWSKY TYPE", "pachyonychia congenita, Jadassohn-Lewandowsky type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pachyonychia congenita", "shortest_name_length": 2}
{"curie": "UMLS:C0349568", "names": ["Palate SCC", "SCC of Palate", "SCC of the Palate", "PALATE CANCER SQUAMOUS CELL", "Palate Squamous Cell Carcinoma", "Squamous cell carcinoma of palate", "Squamous Cell Carcinoma of Palate", "Squamous Cell Carcinoma of the Palate", "SCC - Squamous cell carcinoma of palate", "Squamous cell carcinoma of palate (disorder)", "Squamous cell carcinoma of palate (diagnosis)", "palate neoplasm malignant carcinoma squamous cell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Squamous cell carcinoma of palate", "shortest_name_length": 10}
{"curie": "MONDO:0044634", "names": ["SHRF", "SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES", "short stature, hearing loss, retinitis pigmentosa, and distinctive facies", "retinitis pigmentosa-deafness-premature aging-short stature-facial dysmorphism syndrome", "retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C1857342", "names": ["Deafness, Cochlear, with Myopia and Intellectual Impairment"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Deafness, Cochlear, with Myopia and Intellectual Impairment", "shortest_name_length": 59}
{"curie": "MONDO:0021568", "names": ["TUBULAR", "Tubulonephrosis", "Nephropathy tubular", "NEPHROPATHY TUBULAR", "Renal tubular defect", "renal tubular defect", "renal tubule disease", "Renal tubular disease", "renal tubular disease", "renal tubule disorder", "renal tubular disorder", "Renal tubular disorder", "RENAL TUBULAR DISORDER", "KIDNEY TUBULE DISORDER", "Kidney tubule disorder", "Disorder tubular kidney", "renal; disease, tubular", "DISORDER TUBULAR KIDNEY", "KIDNEY TUBULAR DISORDER", "disease of renal tubule", "Kidney tubular disorder", "disorder of renal tubule", "Renal tubular defect, NOS", "renal tubular dysfunction", "Renal tubular dysfunction", "Renal tubular disorder NOS", "dysfunction; renal tubular", "Renal tubular disorder, NOS", "tubulo-renal function; impaired", "Renal tubular defect (disorder)", "renal tubule disease or disorder", "renal tubular defect (diagnosis)", "Renal tubular disorder (disorder)", "renal tubular disorder (diagnosis)", "disease or disorder of renal tubule", "disease (or disorder); kidney, tubular function", "disease (or disorder); kidney, functional (tubular)", "Abnormal function of filtrating structures in kidney", "Disorders resulting from impaired renal tubular function", "Disorder resulting from impaired renal tubular function, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal tubule disorder", "shortest_name_length": 7}
{"curie": "UMLS:C5206437", "names": ["Stage IA1 Cervical Cancer FIGO 2018", "Stage IA1 Cervical Carcinoma FIGO 2018"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA1 Cervical Cancer FIGO 2018", "shortest_name_length": 35}
{"curie": "UMLS:C1096184", "names": ["WNV", "West Nile virus", "West Nile Virus", "West Nile virus NOS", "west nile viral infection", "West Nile viral infection", "West Nile virus infection, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "West Nile viral infection", "shortest_name_length": 3}
{"curie": "MONDO:0010717", "names": ["PDHAD", "PDH deficiency", "Ataxia with Lactic Acidosis", "ATAXIA WITH LACTIC ACIDOSIS I", "ataxia with lactic acidosis 1", "Ataxia with Lactic Acidosis I", "pyruvate decarboxylase deficiency", "Pyruvate decarboxylase deficiency", "Type I Ataxia with Lactic Acidosis", "Lactic Acidosis with Ataxia, Type I", "Ataxia with Lactic Acidosis, Type I", "lactic acidemia, thiamine-responsive", "LACTIC ACIDEMIA, THIAMINE-RESPONSIVE", "Lactic Acidemia, Thiamine Responsive", "pyruvate dehydrogenase Complex deficiency", "PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY", "Pyruvate Dehydrogenase E1 Alpha Deficiency", "pyruvate dehydrogenase E1-ALPHA deficiency", "pyruvate dehydrogenase E1-alpha deficiency", "Pyruvate dehydrogenase E1-alpha deficiency", "pyruvate dehydrogenase E1-alpha deficiency (diagnosis)", "ataxia, intermittent, with abnormal pyruvate metabolism", "ataxia, intermittent, with pyruvate dehydrogenase deficiency", "pyruvate dehydrogenase e1-alpha deficiency, X-linked dominant", "pyruvate dehydrogenase complex E1 component subunit alpha deficiency", "Pyruvate dehydrogenase complex E1 component subunit alpha deficiency", "ataxia, intermittent, with pyruvate dehydrogenase, or decarboxylase, deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyruvate dehydrogenase E1-alpha deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0000379", "names": ["malignant Sertoli-Leydig cell tumor", "Sertoli-Leydig cell tumor, malignant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant Sertoli-Leydig cell tumor", "shortest_name_length": 35}
{"curie": "MONDO:0009540", "names": ["lymphokine deficiency", "Lymphokine Deficiency", "LYMPHOKINE DEFICIENCY", "chronic mucocutaneous candidiasis due to lymphokine deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic mucocutaneous candidiasis due to lymphokine deficiency", "shortest_name_length": 21}
{"curie": "UMLS:C1699208", "names": ["intraoperative hepatobiliary injury", "Intraoperative hepatobiliary injury", "Intraoperative Hepatobiliary Injury", "intraoperative hepatobiliary injury (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraoperative Hepatobiliary Injury", "shortest_name_length": 35}
{"curie": "UMLS:C0345017", "names": ["Pulmonary Trunk Hypoplasia", "Pulmonary trunk hypoplasia", "Pulmonary trunk hypoplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pulmonary trunk hypoplasia", "shortest_name_length": 26}
{"curie": "MONDO:0009865", "names": ["GSDX", "Gsd10", "GSD10", "Gsd X", "GSD X", "GSD 10", "GSD type 10", "Pgam Deficiency", "PGAM deficiency", "Dimauro disease", "PGAMM deficiency", "PGAMM DEFICIENCY", "glycogen storage disease X", "Glycogen Storage Disease X", "GLYCOGEN STORAGE DISEASE X", "glycogen storage disease 10", "Phosphoglucomutase deficiency", "PGAM2 glycogen storage disease", "glycogen storage disease type X", "Glycogen storage disease type X", "Glycogen storage disease, type X", "Deficiency of phosphoglucomutase", "glycogen storage disease type 10", "Phosphoglycerate mutase deficiency", "Deficiency Mutase Phosphoglycerate", "Phosphoglycerate Mutase Deficiency", "Deficiency of glucose phosphomutase", "muscle phosphoglycerate mutase deficiency", "Muscle phosphoglycerate mutase deficiency", "Glycogen storage disease type X (disorder)", "Deficiency of phosphoglucomutase (disorder)", "glycogen storage disease type X (diagnosis)", "GSD due to phosphoglycerate mutase deficiency", "Phosphoglycerate mutase, muscle, deficiency of", "PHOSPHOGLYCERATE MUTASE, MUSCLE, DEFICIENCY OF", "Phosphoglycerate Mutase, Muscle, Deficiency of", "Human muscle phosphoglycerate mutase deficiency", "myopathy due to phosphoglycerate mutase deficiency", "Myopathy due to phosphoglycerate mutase deficiency", "MYOPATHY DUE TO PHOSPHOGLYCERATE MUTASE DEFICIENCY", "myopathy due to Phosphoglycerate mutase deficiency", "glycogen storage disease caused by mutation in PGAM2", "Muscle phosphoglycerate mutase deficiency (disorder)", "Glycogenosis due to inactive phosphorylase and kinase", "Glycogenosis due to inactive phosphorylase AND kinase", "glycogenosis due to phosphoglycerate mutase deficiency", "Glycogenosis due to phosphoglycerate mutase deficiency", "Glycogen storage disease due to phosphoglycerate mutase deficiency", "glycogen storage disease due to phosphoglycerate mutase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease due to phosphoglycerate mutase deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0005180", "names": ["parkinson's", "Shaking Palsy", "Shaking palsy", "shaking palsy", "PALSY SHAKING", "palsy shaking", "shaking; palsy", "PALSY, SHAKING", "palsy; shaking", "Parkinson disease", "Paralysis Agitans", "Paralysis;agitans", "PARALYSIS AGITANS", "Paralysis agitans", "PARKINSON DISEASE", "paralysis agitans", "Parkinson Disease", "diseases parkinson", "agitans; paralysis", "Parkinsons disease", "paralysis; agitans", "Parkinsons Disease", "Disease;Parkinsons", "DISEASE PARKINSON'S", "Parkinson`s disease", "Parkinson's disease", "parkinson s disease", "Disease Parkinson's", "Parkinson's Disease", "PARKINSON'S DISEASE", "parkinson's disease", "disease parkinson s", "diseases parkinsons", "diseases parkinson's", "SYNDROME PARKINSON'S", "disease parkinsons's", "PARKINSON'S SYNDROME", "Parkinson's syndrome", "Primary parkinsonism", "Primary Parkinsonism", "parkinson's syndrome", "syndrome parkinson's", "Parkinsonism, Primary", "Parkinson disease (PD)", "Idiopathic parkinsonism", "Parkinson's disease NOS", "Idiopathic Parkinsonism", "Parkinson's disease, NOS", "PD - Parkinson's disease", "Lewy Body Parkinson Disease", "parkinson disease lewy body", "idiopathic parkinson disease", "Idiopathic Parkinson Disease", "obsolete_Parkinson's disease", "Parkinson Disease, Idiopathic", "disease idiopathic parkinsons", "disease disorders parkinson's", "Lewy Body Parkinson's Disease", "Parkinson disease (diagnosis)", "Idiopathic Parkinson's Disease", "PARALYSIS AGITANS PARKINSONISM", "idiopathic parkinson's disease", "Parkinson's Disease, Lewy Body", "Parkinson's disease (disorder)", "Idiopathic Parkinson's disease", "Parkinson's Disease, Idiopathic", "bodies disease lewy parkinson's", "PARALYSIS AGITANS <PARKINSONISM>"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parkinson disease", "shortest_name_length": 11}
{"curie": "UMLS:C4521822", "names": ["IIIB", "Stage IIIB Hilar Cholangiocarcinoma", "Stage IIIB Hilar Cholangiocarcinoma AJCC v8", "Stage IIIB Perihilar Cholangiocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Hilar Cholangiocarcinoma AJCC v8", "shortest_name_length": 4}
{"curie": "UMLS:C5447321", "names": ["Combined Immunodeficiencies Associated with Syndromic Features", "Combined Cellular and Humoral Immunodeficiencies Associated with Syndromic Features", "Immunodeficiencies Affecting Cellular and Humoral Immunity Associated with Syndromic Features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Combined Immunodeficiencies Associated with Syndromic Features", "shortest_name_length": 62}
{"curie": "MONDO:0002278", "names": ["Colonic Mass", "colonic Mass", "colonic tumor", "Colonic tumor", "colon neoplasm", "neoplasm of colon", "Benign Colon Tumor", "colon benign tumor", "benign colon tumor", "benign colon tumors", "Benign Colonic Tumor", "benign colonic tumor", "benign colon neoplasm", "benign tumor of colon", "Benign Tumor of Colon", "Benign Colon Neoplasm", "Benign tumor of colon", "colon benign neoplasm", "Benign tumour of colon", "colonic benign neoplasm", "Benign Colonic Neoplasm", "Benign colonic neoplasm", "benign colonic neoplasm", "Benign neoplasm of colon", "benign neoplasm of colon", "Benign Neoplasm of Colon", "Benign Tumor of the Colon", "benign tumor of the colon", "Benign Neoplasm of the Colon", "benign neoplasm of the colon", "Benign neoplasm of colon, NOS", "Benign neoplasm of colon (disorder)", "Benign neoplasm of colon, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign colon neoplasm", "shortest_name_length": 12}
{"curie": "MONDO:0016035", "names": ["ROES", "Nelson", "dermal Ridges", "Nelson syndrome", "Nelson Syndrome", "nelson syndrome", "NELSON SYNDROME", "nelsons syndrome", "Nelson's syndrome", "nelson's syndrome", "Dermal Ridges-Off-The-End", "DERMAL RIDGES-OFF-THE-END", "Nelson syndrome (disorder)", "Ridges-off-the-end syndrome", "RIDGES-OFF-THE-END SYNDROME", "Post adrenalectomy syndrome", "Nelson's syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nelson syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0002567", "names": ["Trachea", "disease trachea", "trachea disease", "Tracheal disease", "Tracheal Disease", "diseases trachea", "tracheal disease", "trachea diseases", "trachea; disease", "Tracheal disorder", "Disease, Tracheal", "Tracheal Diseases", "Tracheal Disorder", "Trachea--Diseases", "tracheal diseases", "tracheal disorder", "Tracheal Disorders", "Windpipe disorders", "disease of trachea", "disorders tracheal", "Diseases, Tracheal", "Windpipe Disorders", "disorder of trachea", "Disorder of Trachea", "Disorder of trachea", "diseases of the trachea", "Disease of trachea, NOS", "DISEASES OF THE TRACHEA", "Abnormality of the trachea", "trachea disease or disorder", "Abnormal trachea morphology", "Abnormal tracheal morphology", "Disorder of trachea (disorder)", "disease or disorder of trachea", "disease (or disorder); trachea", "disorder of trachea (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tracheal disorder", "shortest_name_length": 7}
{"curie": "MONDO:0013023", "names": ["OFC12", "OROFACIAL CLEFT 12", "Orofacial Cleft 12", "orofacial cleft 12", "nonsyndromic cleft lip with or without cleft palate 12", "Cleft Lip with or without Cleft Palate, Nonsyndromic, 12", "cleft lip with or without cleft palate, nonsyndromic, 12", "CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orofacial cleft 12", "shortest_name_length": 5}
{"curie": "UMLS:C5400765", "names": ["Salivary Gland Poorly Differentiated Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Salivary Gland Poorly Differentiated Carcinoma", "shortest_name_length": 46}
{"curie": "MONDO:0002028", "names": ["character neurosis", "character disorder", "Character disorder", "neurosis; character", "character disorders", "character; neurosis", "disorder; character", "Character Disorders", "character; disorder", "Disorder;personality", "DISORDER PERSONALITY", "Personality Disorder", "PERSONALITY DISORDER", "Personality disorder", "personality disorder", "Disorder personality", "personality disorders", "Personality disorders", "PERSONALITY DISORDERS", "Personality Disorders", "Character neurosis NOS", "Character disorder NOS", "psychopathy; personality", "Personality disorder NOS", "personality; psychopathy", "Personality disorder, NOS", "other personality disorder", "Disturbance in personality", "Other personality disorders", "personality disorder (disease)", "Personality disorder (disorder)", "unspecified personality disorder", "Unspecified personality disorder", "personality disorder (diagnosis)", "Personality disorder, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "personality disorder", "shortest_name_length": 18}
{"curie": "MONDO:0008358", "names": ["Goldblatt-Viljoen syndrome", "Goldblatt Viljoen syndrome", "Radial ray hypoplasia choanal atresia", "radial ray hypoplasia choanal atresia", "Goldblatt Viljoen radial ray hypoplasia", "radial ray hypoplasia and choanal atresia", "radial RAY hypoplasia with choanal atresia", "Choanal atresia with radial ray hypoplasia", "Radial Ray Hypoplasia with Choanal Atresia", "RADIAL RAY HYPOPLASIA WITH CHOANAL ATRESIA", "Radial ray hypoplasia with choanal hypoplasia", "Radial ray hypoplasia-choanal atresia syndrome", "radial ray hypoplasia-choanal atresia syndrome", "Autosomal dominant radial ray hypoplasia syndrome", "Choanal atresia with radial ray hypoplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radial ray hypoplasia-choanal atresia syndrome", "shortest_name_length": 26}
{"curie": "UMLS:C1699136", "names": ["Gastric Mucositis", "Gastric mucositis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric mucositis", "shortest_name_length": 17}
{"curie": "MONDO:0019724", "names": ["secondary glomerular disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary glomerular disease", "shortest_name_length": 28}
{"curie": "UMLS:C2747795", "names": ["Vertebral foraminal stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vertebral foraminal stenosis", "shortest_name_length": 28}
{"curie": "UMLS:C2242574", "names": ["Compulsive sexual behavior", "Compulsive sexual behaviour"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Compulsive sexual behaviour", "shortest_name_length": 26}
{"curie": "MONDO:0032626", "names": ["MC1DN22", "nuclear type mitochondrial complex I deficiency 22", "mitochondrial complex 1 deficiency, nuclear type 22", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 22"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 22", "shortest_name_length": 7}
{"curie": "UMLS:C1708772", "names": ["Lung Glandular Papilloma", "Glandular papilloma of lung", "Bronchial Glandular Papilloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Glandular papilloma of lung", "shortest_name_length": 24}
{"curie": "MONDO:0009613", "names": ["MMA Cbl A type", "cobalamin B disease", "Cobalamin B disease", "cobalamin A disease", "Cobalamin A disease", "CblB - Cobalamin locus B", "cblA - cobalamin locus a", "cblB - cobalamin locus b", "CblA - Cobalamin locus A", "cobalamin locus B variant", "Cobalamin locus A variant", "Cobalamin locus B variant", "cobalamin locus A variant", "CblB methylmalonic acidemia", "cblB methylmalonic acidemia", "cblA methylmalonic acidemia", "CblA methylmalonic acidemia", "CblB methylmalonic acidaemia", "CblA methylmalonic acidaemia", "Cobalamin B disease (disorder)", "Cobalamin A disease (disorder)", "cobalamin A disease (diagnosis)", "cobalamin B disease (diagnosis)", "methylmalonic aciduria cblA type", "Methylmalonic acidemia cblA type", "methylmalonic acidemia cblA type", "Methylmalonic aciduria cblA type", "METHYLMALONIC ACIDURIA, cblA TYPE", "METHYLMALONIC ACIDEMIA, cblA TYPE", "methylmalonic aciduria, cblA type", "methylmalonic acidemia, cblA type", "Methylmalonic Acidemia, cblA Type", "Methylmalonic Aciduria, cblA Type", "vitamin B12-responsive methylmalonic acidemia type cblA", "vitamin B12-responsive methylmalonic aciduria type cblA", "Vitamin B12-responsive methylmalonic acidemia type cblA", "Vitamin B12-responsive methylmalonic aciduria type cblA", "Methylmalonic aciduria, vitamin B12-responsive, cblA type", "METHYLMALONIC ACIDURIA, VITAMIN B12-RESPONSIVE, DUE TO DEFECT IN SYNTHESIS OF ADENOSYLCOBALAMIN, cblA TYPE", "methylmalonic aciduria, vitamin B12-responsive due to a defect in synthesis of adenosylcobalamin cb1A type", "methylmalonic aciduria, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin, cblA type", "methylmalonic aciduria, vitamin B12-responsive due to a defect in synthesis of adenosylcobalamin cblA type", "methylmalonic aciduria, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin, cblA complementation type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "methylmalonic aciduria, cblA type", "shortest_name_length": 14}
{"curie": "UMLS:C0162351", "names": ["Contact hypersensitivity", "contact hypersensitivity", "Contact Hypersensitivity", "Hypersensitivity, Contact", "Hypersensitivity, contact", "Contact Hypersensitivities", "Hypersensitivities, Contact", "Contact hypersensitivity (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Contact hypersensitivity", "shortest_name_length": 24}
{"curie": "UMLS:C4682657", "names": ["Stage II Gestational Trophoblastic Neoplasm AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Gestational Trophoblastic Neoplasm AJCC v8", "shortest_name_length": 51}
{"curie": "MONDO:0004943", "names": ["orbit sarcoma", "Orbit Sarcoma", "orbital sarcoma", "Orbital Sarcoma", "sarcoma of orbit", "Sarcoma of orbit", "Sarcoma of Orbit", "sarcoma of the orbit", "Sarcoma of the Orbit", "orbit of skull sarcoma", "sarcoma of orbit of skull", "Sarcoma of orbit (disorder)", "sarcoma of orbit (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orbit sarcoma", "shortest_name_length": 13}
{"curie": "MONDO:0013083", "names": ["NBLST3", "ALK neuroblastoma", "susceptibility to neuroblastoma 3", "NEUROBLASTOMA, SUSCEPTIBILITY TO, 3", "neuroblastoma, susceptibility to, 3", "neuroblastoma caused by mutation in ALK", "neuroblastoma, susceptibility to, type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuroblastoma, susceptibility to, 3", "shortest_name_length": 6}
{"curie": "UMLS:C0311375", "names": ["poison arsenic", "arsenic poison", "Arsenic toxicity", "Arsenic poisoning", "Arsenic Poisoning", "arsenic poisoning", "poisonings arsenic", "Arsenical toxicity", "Arsenic Poisonings", "Poisoning, Arsenic", "Poisonings, Arsenic", "poisoning by arsenic", "Toxic effect of arsenic", "Arsenic poisoning syndrome", "Arsenic causing toxic effect", "poisoning by arsenic (diagnosis)", "Arsenical Neurotoxicity Syndrome", "Arsenic Poisoning, Nervous System", "Arsenical Neurotoxicity Syndromes", "Nervous System Poisoning, Arsenic", "Neurotoxicity Syndrome, Arsenical", "Syndrome, Arsenical Neurotoxicity", "Neurotoxicity Syndromes, Arsenical", "Syndromes, Arsenical Neurotoxicity", "Poisoning, Arsenic, Nervous System", "Toxic effect of arsenic and its compounds", "Toxic effect of arsenic and its compounds NOS", "Toxic effect of arsenic and its compounds, NOS", "Toxic effect of arsenic and/or arsenic compound", "Arsenic or arsenic compound causing toxic effect", "Toxic effect of arsenic and/or arsenic compound (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arsenic Poisoning", "shortest_name_length": 14}
{"curie": "UMLS:C0948610", "names": ["Abdominal strangulated hernia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abdominal strangulated hernia", "shortest_name_length": 29}
{"curie": "MONDO:0012841", "names": ["IBD18", "INFLAMMATORY BOWEL DISEASE 18", "Inflammatory Bowel Disease 18", "inflammatory bowel disease 18", "inflammatory bowel disease type 18"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory bowel disease 18", "shortest_name_length": 5}
{"curie": "UMLS:C3897231", "names": ["Untreated Glioblastoma", "untreated childhood glioblastoma", "Untreated Childhood Glioblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Untreated Childhood Glioblastoma", "shortest_name_length": 22}
{"curie": "UMLS:C4688308", "names": ["Advanced Non-Squamous Non-Small Cell Lung Cancer", "Advanced Non-Squamous Non-Small Cell Lung Carcinoma", "Advanced Lung Non-Squamous Non-Small Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Lung Non-Squamous Non-Small Cell Carcinoma", "shortest_name_length": 48}
{"curie": "UMLS:C4331004", "names": ["Pharyngeal Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pharyngeal Carcinoma by AJCC v8 Stage", "shortest_name_length": 37}
{"curie": "MONDO:0003847", "names": ["Genetic disease", "genetic disease", "Genetic Disease", "inborn disorder", "Genetic Disorder", "syndrome genetic", "genetic disorder", "genetics disease", "Genetic diseases", "Genetic disorder", "Genetic Diseases", "Disease, Genetic", "Genetic Syndrome", "Genetic syndrome", "GENETIC DISORDER", "genetic syndrome", "Disorder, Genetic", "genetic condition", "genetic syndromes", "Inherited disease", "inherited disease", "molecular disease", "genetics syndrome", "Diseases, Genetic", "Mendelian disease", "Inherited Disease", "familial disorder", "genetic disorders", "Genetic.Disorders", "Genetic Disorders", "Genetic condition", "Genetic disorders", "Genetic Condition", "Molecular Disease", "Hereditary Disease", "genetics syndromes", "Hereditary disease", "heritable disorder", "hereditary disease", "Disorders, Genetic", "Disease, Hereditary", "Hereditary disorder", "Hereditary Diseases", "diseases hereditary", "hereditary disorder", "hereditary diseases", "HEREDITARY DISORDER", "Hereditary Disorders", "hereditary disorders", "Diseases, Hereditary", "Genetic disease, NOS", "inborn genetic disease", "Inborn Genetic Disease", "Inherited disease, NOS", "Genetic Disease, Inborn", "Hereditary disease, NOS", "Hereditary disorder NOS", "Inborn Genetic Diseases", "Disease, Inborn Genetic", "Diseases, Inborn Genetic", "Genetic Diseases, Inborn", "syndrome genetic disorder", "inherited genetic disease", "genetic disorder syndrome", "Genetic disease (disorder)", "disorders genetic syndrome", "Hereditary disease (disorder)", "hereditary disease or disorder", "Hereditary disorder, congenital"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary disease", "shortest_name_length": 15}
{"curie": "MONDO:0019176", "names": ["trichorhinophalangeal syndrome type 1 and 3", "trichorhinophalangeal syndrome type I or III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichorhinophalangeal syndrome type I or III", "shortest_name_length": 43}
{"curie": "MONDO:0032765", "names": ["BDPLT22", "bleeding disorder, platelet-type, 22", "BLEEDING DISORDER, PLATELET-TYPE, 22"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bleeding disorder, platelet-type, 22", "shortest_name_length": 7}
{"curie": "MONDO:0011448", "names": ["FPLD3", "PPARG-related FPLD", "insulin resistance, severe, digenic", "Familial partial lipodystrophy type 3", "familial partial lipodystrophy type 3", "Familial Partial Lipodystrophy, Type 3", "lipodystrophy, familial partial, type 3", "LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3", "Lipodystrophy, Familial Partial, Type 3", "PPARG-related familial partial lipodystrophy", "FPLD3 - familial partial lipodystrophy type 3", "familial partial lipodystrophy associated with PPARG mutations", "lipodystrophy, familial partial, associated with Pparg mutations", "Lipodystrophy, Familial Partial, Associated With PPARg Mutations", "LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PPARG MUTATIONS", "Peroxisome proliferator activated receptor gamma-related familial partial lipodystrophy", "Peroxisome proliferator activated receptor gamma-related familial partial lipodystrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PPARG-related familial partial lipodystrophy", "shortest_name_length": 5}
{"curie": "UMLS:C0265029", "names": ["v.portae; block", "portal obstruction", "Portal obstruction", "block; portal vein", "portal; obstruction", "obstruction; portal", "Portal vein occlusion", "v.portae; obstruction", "portal vein obstruction", "PORTAL VEIN OBSTRUCTION", "Portal vein obstruction", "Portal (vein) obstruction", "Portal vein obstruction, NOS", "Hepatic portal vein obstruction", "Occlusion of hepatic portal vein", "obstruction of hepatic portal vein", "Portal vein obstruction (disorder)", "obstruction; vein, vein, venous, portal", "disorder of vein obstruction hepatic portal", "obstruction of hepatic portal vein (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Portal vein obstruction", "shortest_name_length": 15}
{"curie": "UMLS:C5419607", "names": ["Advanced Marginal Zone Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Marginal Zone Lymphoma", "shortest_name_length": 31}
{"curie": "MONDO:0017913", "names": ["Pure or complex familial spastic paraplegia", "pure or complex hereditary spastic paraplegia", "Pure or complicated familial spastic paraplegia", "Pure or complicated hereditary spastic paraplegia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pure or complex hereditary spastic paraplegia", "shortest_name_length": 43}
{"curie": "UMLS:C5556837", "names": ["Early-Stage Triple-Negative Breast Carcinoma", "Early Stage Triple-Negative Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Early Stage Triple-Negative Breast Carcinoma", "shortest_name_length": 44}
{"curie": "MONDO:0001165", "names": ["hypoglossia", "Hypoglossia", "Microglossia", "Small tongue", "microglossia", "Microglossias", "Tongue Disease", "Tongue disease", "tongue disease", "disease tongue", "Disorder tongue", "Tongue Disorder", "tongue diseases", "tongue disorder", "diseases tongue", "Tongue disorder", "Disease, Tongue", "DISORDER TONGUE", "TONGUE DISORDER", "Tongue Diseases", "Tongue--Diseases", "Tongue disorders", "disorders tongue", "Tongue Disorders", "tongue; disorder", "Diseases, Tongue", "disease of tongue", "Tongue hypoplasia", "Disease of tongue", "Lingual hypoplasia", "Rudimentary tongue", "Hypoplastic tongue", "Disorder of tongue", "Diseases of tongue", "tongue; hypoplasia", "hypoplasia; tongue", "diseases of tongue", "disorder of tongue", "tongue microglossia", "Tongue disorder NOS", "Tongue disorder, NOS", "Hypoplasia of tongue", "hypoplasia of tongue", "diseases of the tongue", "Small tongue (finding)", "Disease of tongue, NOS", "DISEASES OF THE TONGUE", "Abnormally small tongue", "Microglossia (disorder)", "tongue disorder disease", "Decreased size of tongue", "Hypoplasia of the tongue", "microglossia (diagnosis)", "Microglossia - congenital", "tongue disease or disorder", "disease or disorder of tongue", "Disorder of tongue (disorder)", "disease (or disorder); tongue", "Disease of tongue, unspecified", "Underdevelopment of the tongue", "disorder of tongue (diagnosis)", "microglossia (physical finding)", "Isolated congenital hypoglossia", "Congenital hypoplasia of tongue", "Unspecified condition of the tongue", "hypoplasia of tongue (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tongue disorder", "shortest_name_length": 11}
{"curie": "MONDO:0000156", "names": ["Trigonocephaly", "trigonocephaly", "Trigonocephalus", "trigonocephalus", "trigonocephalia", "Trigonocephalia", "Triangular skull", "Wedge shaped head", "Wedge shaped skull", "Wedge shaped cranium", "Triangular head shape", "Triangular skull shape", "Isolated trigonocephaly", "trigonocephaly, isolated", "Triangular cranium shape", "Trigonocephaly (disorder)", "trigonocephaly (diagnosis)", "Isolated metopic craniosynostosis", "Non-syndromic metopic craniosynostosis", "Non-syndromic metopic suture synostosis", "congenital anomaly of frontal bone trigonocephaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trigonocephaly", "shortest_name_length": 14}
{"curie": "UMLS:C0278775", "names": ["Recurrent Liver Cancer", "Relapsed Adult Liver Cancer", "Recurrent Adult Liver Cancer", "Recurrent Adult Liver Carcinoma", "Relapsed Adult Primary Liver Cancer", "Recurrent Adult Primary Liver Cancer", "recurrent adult primary liver cancer", "adult primary liver cancer, recurrent", "liver cancer, recurrent adult primary", "Relapsed Adult Primary Cancer of Liver", "Recurrent Adult Primary Cancer of Liver", "Relapsed Adult Primary Cancer of the Liver", "Recurrent Adult Primary Cancer of the Liver"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Adult Liver Carcinoma", "shortest_name_length": 22}
{"curie": "MONDO:0015054", "names": ["HAE2", "HAE 2", "HAE-II", "ANGIOEDEMA, HEREDITARY, 2", "hereditary angioedema type 2", "Hereditary Angioedema Type II", "Hereditary angioedema type II", "ANGIOEDEMA, HEREDITARY, TYPE II", "Angioedema, Hereditary, Type II", "hereditary angioneurotic edema type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary angioedema type 2", "shortest_name_length": 4}
{"curie": "MONDO:0015211", "names": ["isolated intestinal malformation", "nonsyndromic intestinal malformation", "non-syndromic intestinal malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-syndromic intestinal malformation", "shortest_name_length": 32}
{"curie": "MONDO:0006722", "names": ["Fluorosis", "fluorosis", "TEETH MOTTLED", "Teeth mottled", "Mottled teeth", "Mottled tooth", "mottled teeth", "Mottled Enamel", "TEETH MOTTLING", "Mottled enamel", "mottled enamel", "Tooth mottling", "Teeth mottling", "Mottling enamel", "MOTTLING ENAMEL", "Enamel mottling", "ENAMEL MOTTLING", "Enamel, Mottled", "Mottled Enamels", "Dental Fluorosis", "Dental fluorosis", "Dental Fluoroses", "dental fluorosis", "fluorosis dental", "FLUOROSIS DENTAL", "Fluorosis dental", "dental; fluorosis", "Fluorosis, Dental", "fluorosis; dental", "Fluoroses, Dental", "mottling of enamel", "Mottling of enamel", "Diffuse enamel opacities", "Mottled teeth (disorder)", "mottled teeth (diagnosis)", "Dental Fluorosis, Acquired", "Dental fluorosis (disorder)", "dental fluorosis (diagnosis)", "Intrinsic enamel discoloration of fluorosis", "Intrinsic enamel discolouration of fluorosis", "intrinsic enamel discolouration of fluorosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dental fluorosis", "shortest_name_length": 9}
{"curie": "MONDO:0008969", "names": ["Cholesterol pneumonia", "CHOLESTEROL PNEUMONIA", "cholesterol pneumonia", "pneumonia cholesterol", "pneumonia; cholesterol", "Pneumonia, cholesterol", "cholesterol; pneumonia", "Cholesterol pneumonia (disorder)", "Familiaere Cholesterin-Pneumonie", "familiaere cholesterin-Pneumonie", "Cholesterol pneumonia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholesterol pneumonia", "shortest_name_length": 21}
{"curie": "MONDO:0000778", "names": ["fruit allergy", "Fruit Allergy", "Fruit allergy", "Allergy, Fruit", "allergies fruit", "allergies fruits", "Allergy to fruit", "allergy to fruit", "Allergy to fruit, NOS", "Allergy to fruit (finding)", "allergy to fruit (history)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fruit allergy", "shortest_name_length": 13}
{"curie": "MONDO:0014209", "names": ["NDGOA", "SPG79", "SPG79B", "hereditary spastic paraplegia 79B", "spastic paraplegia 79 autosomal recessive", "spastic paraplegia 79, autosomal recessive", "autosomal recessive spastic paraplegia 79B", "SPASTIC PARAPLEGIA 79B, AUTOSOMAL RECESSIVE", "neurodegeneration with optic atrophy, childhood-onset", "NEURODEGENERATION WITH OPTIC ATROPHY, CHILDHOOD-ONSET", "early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0012347", "names": ["Pcfh", "PCFH", "Precalcaneal congenital fibrolipomatous hamartoma", "hamartoma, Precalcaneal congenital fibrolipomatous", "HAMARTOMA, PRECALCANEAL CONGENITAL FIBROLIPOMATOUS", "Hamartoma, Precalcaneal Congenital Fibrolipomatous"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hamartoma, Precalcaneal congenital fibrolipomatous", "shortest_name_length": 4}
{"curie": "MONDO:0013779", "names": ["WAS2", "WIP Deficiency", "WIP DEFICIENCY", "WIPF1 DEFICIENCY", "Wipf1 deficiency", "Wiskott-Aldrich syndrome 2", "WISKOTT-ALDRICH SYNDROME 2", "Wiskott-Aldrich Syndrome 2", "WIPF1 Wiskott-Aldrich syndrome", "Wiskott-Aldrich syndrome type 2", "Wiskott-Aldrich syndrome caused by mutation in WIPF1", "Wiskott-Aldrich Syndrome Interacting Protein Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wiskott-Aldrich syndrome 2", "shortest_name_length": 4}
{"curie": "UMLS:C1112629", "names": ["Adenoviral hemorrhagic cystitis", "Adenoviral haemorrhagic cystitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenoviral hemorrhagic cystitis", "shortest_name_length": 31}
{"curie": "MONDO:0004348", "names": ["retinal telangiectasia", "Retinal telangiectasia", "retinal telangiectasias", "telangiectasia of retina", "Telangiectasia of the retina", "Retinal telangiectasia (disorder)", "retinal telangiectasia (diagnosis)", "Retinal grouped capillary aneurysms", "telangiectasia of retina (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal telangiectasia", "shortest_name_length": 22}
{"curie": "MONDO:0007707", "names": ["small intestine hemangioma", "hemangioma of small intestine", "Hemangiomas of Small Intestine", "HEMANGIOMAS OF SMALL INTESTINE", "hemangiomas of small intestine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemangiomas of small intestine", "shortest_name_length": 26}
{"curie": "UMLS:C1333973", "names": ["Liver Non-Hodgkin Lymphoma", "Hepatic Non-Hodgkin Lymphoma", "Non-Hodgkin's Liver Lymphoma", "Hepatic Non-Hodgkin's Lymphoma", "non-Hodgkin's lymphoma of liver", "Non-Hodgkin's Lymphoma of Liver", "Primary Liver Non-Hodgkin Lymphoma", "Non-Hodgkin's Lymphoma of the Liver", "Primary Hepatic Non-Hodgkin's Lymphoma", "non-Hodgkin's lymphoma of liver (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-Hodgkin's lymphoma of liver", "shortest_name_length": 26}
{"curie": "UMLS:C0751829", "names": ["Sensorimotor Gait Disorder", "Gait Disorder, Sensorimotor", "Sensorimotor Gait Disorders", "Gait Disorders, Sensorimotor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gait Disorder, Sensorimotor", "shortest_name_length": 26}
{"curie": "MONDO:0009771", "names": ["OTD", "OCULOTRICHODYSPLASIA", "oculotrichodysplasia", "Oculotrichodysplasia", "Oculotrichodysplasia (disorder)", "Cecato de Lima-Pinheiro syndrome", "Cecatto de Lima Pinheiro syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculotrichodysplasia", "shortest_name_length": 3}
{"curie": "MONDO:0035548", "names": ["Autosomal recessive MSMD due to partial JAK1 deficiency", "autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial jak1 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial jak1 deficiency", "shortest_name_length": 55}
{"curie": "MONDO:0010719", "names": ["XNKS", "X-Ray Nk sensitivity", "X-RAY NK SENSITIVITY", "X-Ray NK Sensitivity", "Radiation Sensitivity of Natural Killer Activity", "RADIATION SENSITIVITY OF NATURAL KILLER ACTIVITY", "radiation sensitivity of natural killer activity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radiation sensitivity of natural killer activity", "shortest_name_length": 4}
{"curie": "MONDO:0018593", "names": ["primary PAN", "primary polyarteritis nodosa", "primary periarteritis nodosa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary polyarteritis nodosa", "shortest_name_length": 11}
{"curie": "UMLS:C4054541", "names": ["Drug Associated Membranous Nephropathy", "Membranous Nephropathy - Drug Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Membranous Nephropathy - Drug Associated", "shortest_name_length": 38}
{"curie": "MONDO:0003432", "names": ["Squint", "SQUINT", "phoria", "squint", "Phoria", "phorias", "Phorias", "squinting", "Squinting", "STRABISMUS", "Cross-eyed", "strabismus", "Strabismus", "crossed eye", "Squint, NOS", "Squint eyes", "heterotropia", "Heterotropia", "HETEROTROPIA", "EYE DEVIATION", "Heterotropias", "eye deviation", "Eye deviation", "Strabismus NOS", "deviations eye", "eye; deviation", "Strabismus, NOS", "Heterotropia, NOS", "Ocular dissociation", "squinting (symptom)", "Strabismus (disorder)", "strabismus (diagnosis)", "Unspecified strabismus", "Heterotropia (disorder)", "Strabismus, unspecified", "Unspecified heterotropia", "heterotropia (diagnosis)", "Heterotropia, unspecified", "Other specified strabismus", "Binocular eye movement disorder", "eye; movement disorder (binocular)", "Disorder of binocular eye movements", "Binocular eye movement disorder NOS", "Unspecified disorder of binocular eye movements"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "strabismus", "shortest_name_length": 6}
{"curie": "MONDO:0017212", "names": ["paraneoplastic uveitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paraneoplastic uveitis", "shortest_name_length": 22}
{"curie": "MONDO:0100209", "names": ["X inactivation, familial skewed"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X inactivation, familial skewed", "shortest_name_length": 31}
{"curie": "UMLS:C1334427", "names": ["Grade I PeIN", "Low Grade PeIN", "Grade 1 Penile Intraepithelial Neoplasia", "Grade I Penile Intraepithelial Neoplasia", "Low Grade Penile Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Grade Penile Intraepithelial Neoplasia", "shortest_name_length": 12}
{"curie": "MONDO:0003675", "names": ["posterolateral myocardial infarction", "Posterolateral Myocardial Infarction by EKG Finding", "Posterolateral Myocardial Infarction by ECG Finding"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "posterolateral myocardial infarction", "shortest_name_length": 36}
{"curie": "MONDO:0018205", "names": ["Monosomy 1qter", "monosomy 1qter", "distal monosomy 1q", "Distal deletion 1q", "Distal monosomy 1q", "distal deletion 1q", "Telomeric deletion 1q", "telomeric deletion 1q", "distal monosomy type 1q", "Distal monosomy 1q syndrome", "Distal monosomy 1q syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal monosomy 1q", "shortest_name_length": 14}
{"curie": "MONDO:0005629", "names": ["Amoebic keratitis", "Acanthameba keratitis", "Acanthamoeba Keratitis", "Acanthamoeba keratitis", "Keratitis, Acanthamoeba", "keratitis, Acanthamoeba", "Acanthamoeba Keratitides", "Keratitides, Acanthamoeba", "Acanthamoeba caused keratitis", "Acanthamoeba keratitis (disorder)", "Acanthamoeba keratitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acanthamoeba keratitis", "shortest_name_length": 17}
{"curie": "MONDO:0014262", "names": ["LDS5", "RNHF", "Rienhoff Syndrome", "Reinhoff syndrome", "RIENHOFF SYNDROME", "Rienhoff syndrome", "LOEYS-DIETZ SYNDROME 5", "Loeys-Dietz syndrome 5", "Loeys-Dietz Syndrome Type 5", "Loeys-Dietz syndrome type 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rienhoff syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0020835", "names": ["methemoglobinemia, alpha type", "METHEMOGLOBINEMIA, ALPHA TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "methemoglobinemia, alpha type", "shortest_name_length": 29}
{"curie": "MONDO:0003637", "names": ["CCSTL", "Sugar tumor", "Sugar Tumor", "lung clear cell tumor", "Lung Clear Cell Tumor", "lung clear cell-sugar-tumor", "clear cell-Sugar-tumor of lung", "Clear Cell-Sugar-Tumor of Lung", "clear cell-sugar-tumor of the lung", "clear cell-Sugar-tumor of the lung", "Clear Cell-Sugar-Tumor of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "clear cell-sugar-tumor of the lung", "shortest_name_length": 5}
{"curie": "MONDO:0035684", "names": ["EBS without extracutaneous involvement", "epidermolysis bullosa simplex without extracutaneous involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolysis bullosa simplex without extracutaneous involvement", "shortest_name_length": 38}
{"curie": "UMLS:C4552681", "names": ["I", "Stage I Thyroid Gland Papillary Cancer", "Stage I Thyroid Gland Papillary Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Thyroid Gland Papillary Carcinoma AJCC v8", "shortest_name_length": 1}
{"curie": "MONDO:0006696", "names": ["ectopy cervix", "Cervix Erosion", "erosion cervix", "cervix erosion", "Cervix erosion", "Erosion;cervix", "Erosion, Cervix", "cervix; erosion", "erosion; cervix", "Cervical ectopy", "Ectropion;cervix", "Cervical erosion", "CERVICAL EROSION", "eversion; cervix", "cervix; eversion", "cervical erosion", "cervix ectropion", "Ectopy of cervix", "erosion cervical", "CERVICAL EVERSION", "cervical eversion", "Erosion of cervix", "ectropion; cervix", "cervix; ectropion", "erosion of cervix", "cervical ectropion", "Eversion of cervix", "Cervical ectropion", "Ectropion of cervix", "CERVICAL PROTRUSION", "erosion of the cervix", "Uterine Cervix Erosion", "Erosion uterine cervix", "EROSION UTERINE CERVIX", "cervix erosion uterine", "Cervix Erosion, Uterine", "Erosion, Uterine Cervix", "Uterine Cervical Erosion", "Uterine cervical erosion", "Erosion, Uterine Cervical", "Cervical Erosion, Uterine", "Superficial ulcer of cervix", "Erosion of cervix (disorder)", "erosion of cervix (diagnosis)", "cervical ectropion (diagnosis)", "Ectropion of cervix (disorder)", "cervical erosion (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervix erosion", "shortest_name_length": 13}
{"curie": "UMLS:C0346057", "names": ["Neuroma cutis", "Dermal Neurofibroma", "Cutaneous neurofibroma", "Cutaneous Neurofibroma", "Neurofibromas, cutaneous", "Cutaneous (Skin) Neurofibroma", "Cutaneous neurofibroma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous neurofibroma", "shortest_name_length": 13}
{"curie": "UMLS:C1407280", "names": ["Peripheral artery thrombosis", "peripheral; artery, thrombosis", "thrombosis of peripheral artery", "thrombosis; peripheral arteries", "thrombosis of peripheral artery (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peripheral artery thrombosis", "shortest_name_length": 28}
{"curie": "UMLS:C0854489", "names": ["Prostatic carcinoid tumor", "Prostatic carcinoid tumour", "Carcinoid tumor of the prostate", "Carcinoid tumour of the prostate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carcinoid tumor of the prostate", "shortest_name_length": 25}
{"curie": "MONDO:0001771", "names": ["Infective urethral stricture", "infective urethral stricture", "stricture; urethra, infective", "Urethral stricture due to infection", "urethral stricture due to infection", "Urethral stricture due to infection, NOS", "Urethral stricture due to infection (disorder)", "urethral stricture due to infection (diagnosis)", "Urethral stricture due to unspecified infection", "urethral stricture due to infective disease classified elsewhere", "urethral stricture due to infective diseases classified elsewhere", "Urethral stricture due to infective diseases classified elsewhere", "urethral stricture due to infective disease classified elsewhere (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infective urethral stricture", "shortest_name_length": 28}
{"curie": "MONDO:0000680", "names": ["astereognosia", "somatosensory agnosia", "astereognosia (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "astereognosia", "shortest_name_length": 13}
{"curie": "MONDO:0000620", "names": ["Breast tumor benign", "Benign Breast Tumor", "tumor benign breast", "benign breast tumor", "breast benign tumor", "benign breast tumors", "Breast tumour benign", "benign breast tumours", "benign breasts tumour", "Benign Breast Neoplasm", "benign tumor of breast", "Benign breast neoplasm", "of benign breast tumor", "benign breast neoplasm", "breast benign neoplasm", "Benign tumor of breast", "Benign Tumor of Breast", "benign breast neoplasms", "Benign tumour of breast", "benign breast of tumours", "Benign neoplasm of breast", "Benign Neoplasm of Breast", "benign neoplasm of breast", "Benign breast neoplasm NOS", "benign tumor of the breast", "Benign Tumor of the Breast", "Benign Neoplasm of the Breast", "benign neoplasm of the breast", "Benign tumor of breast (disorder)", "benign neoplasm of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast benign neoplasm", "shortest_name_length": 19}
{"curie": "MONDO:0030317", "names": ["CMH28", "CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 28", "cardiomyopathy, familial hypertrophic, 28"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiomyopathy, familial hypertrophic, 28", "shortest_name_length": 5}
{"curie": "MONDO:0015094", "names": ["Subependymal nodular heterotopia", "subependymal nodular heterotopia", "Subependymal nodular heterotopia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subependymal nodular heterotopia", "shortest_name_length": 32}
{"curie": "MONDO:0007788", "names": ["HYTG1", "HYPERTRIGLYCERIDEMIA 1", "hypertriglyceridemia 1", "HYPERTRIGLYCERIDEMIA, FAMILIAL", "hypertriglyceridemia, familial", "hypertriglyceridemia, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertriglyceridemia 1", "shortest_name_length": 5}
{"curie": "MONDO:0016340", "names": ["Familial restrictive cardiomyopathy", "familial restrictive cardiomyopathy", "hereditary restrictive cardiomyopathy", "Familial restrictive cardiomyopathy (disorder)", "familial restrictive cardiomyopathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial restrictive cardiomyopathy", "shortest_name_length": 35}
{"curie": "UMLS:C1332508", "names": ["Benign Intracranial Meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Intracranial Meningioma", "shortest_name_length": 30}
{"curie": "MONDO:0008604", "names": ["triphalangeal thumb with double phalanges", "TRIPHALANGEAL THUMB WITH DOUBLE PHALANGES", "Triphalangeal Thumb with Double Phalanges"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "triphalangeal thumb with double phalanges", "shortest_name_length": 41}
{"curie": "UMLS:C1377916", "names": ["Benign Vascular Tumor", "benign vascular tumor", "Benign Vascular Neoplasm", "Benign vascular neoplasm", "benign vascular neoplasm", "vascular neoplasms, benign", "Vascular Neoplasms, Benign", "benign adult vascular neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign vascular neoplasm", "shortest_name_length": 21}
{"curie": "MONDO:0002664", "names": ["Signet Ring Cell Bile Duct Carcinoma", "bile duct signet ring cell carcinoma", "Bile Duct Signet Ring Cell Carcinoma", "signet Ring cell bile duct carcinoma", "bile duct signet Ring cell carcinoma", "Bile duct signet-ring cell carcinoma", "Signet Ring Cell Carcinoma of Bile Duct", "signet Ring cell carcinoma of bile duct", "Signet Ring Cell Carcinoma of the Bile Duct", "signet Ring cell carcinoma of the bile duct", "Extrahepatic Bile Duct Signet Ring Cell Carcinoma", "extrahepatic bile duct signet ring cell carcinoma", "extrahepatic bile duct signet Ring cell carcinoma", "Extrahepatic Bile Duct Signet-Ring Cell Carcinoma", "signet ring cell carcinoma of extrahepatic bile duct", "signet ring cell carcinoma of extrahepatic bile duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extrahepatic bile duct signet ring cell carcinoma", "shortest_name_length": 36}
{"curie": "UMLS:C4684942", "names": ["Refractory Thyroid Cancer", "Refractory Thyroid Gland Cancer", "Refractory Thyroid Gland Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Thyroid Gland Carcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0016203", "names": ["hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency", "shortest_name_length": 69}
{"curie": "MONDO:0030673", "names": ["SPG86", "hereditary spastic paraplegia 86", "spastic paraplegia 86 autosomal recessive", "SPASTIC PARAPLEGIA 86, AUTOSOMAL RECESSIVE", "spastic paraplegia 86, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic paraplegia 86, autosomal recessive", "shortest_name_length": 5}
{"curie": "UMLS:C1708751", "names": ["Myofibrosarcoma", "Myofibroblastic sarcoma", "Myofibroblastic Sarcoma", "Low grade myofibroblastic sarcoma", "Low-grade myofibroblastic sarcoma", "Low Grade Myofibroblastic Sarcoma", "Low-Grade Myofibroblastic Sarcoma", "Low grade myofibroblastic sarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low grade myofibroblastic sarcoma", "shortest_name_length": 15}
{"curie": "MONDO:0015383", "names": ["cervicofacial enchondroma", "cervicofacial fibrochondroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervicofacial fibrochondroma", "shortest_name_length": 25}
{"curie": "UMLS:C3898656", "names": ["TYPE 3 MYOCARDIAL INFARCTION", "Myocardial infarction type 3", "Joint Task Force Type 3 Myocardial Infarction", "Joint ESC/ACCF/AHA/WHF Task Force Type 3 Myocardial Infarction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joint Task Force Type 3 Myocardial Infarction", "shortest_name_length": 28}
{"curie": "MONDO:0011868", "names": ["LCCS2", "lethal congenital contracture syndrome 2", "Lethal Congenital Contracture Syndrome 2", "LETHAL CONGENITAL CONTRACTURE SYNDROME 2", "lethal congenital contractural syndrome 2", "ERBB3 lethal congenital contracture syndrome", "Lethal congenital contracture syndrome type 2", "lethal congenital contracture syndrome type 2", "Multiple contracture syndrome Israeli-Bedouin type", "Multiple contracture syndrome, Israeli-Bedouin type", "multiple contracture syndrome, Israeli Bedouin type", "multiple contracture syndrome, Israeli-Bedouin type", "multiple contracture syndrome, Israeli Bedouin type a", "MULTIPLE CONTRACTURE SYNDROME, ISRAELI BEDOUIN TYPE A", "Multiple Contracture Syndrome, Israeli Bedouin Type A", "Lethal congenital contracture syndrome type 2 (disorder)", "lethal congenital contracture syndrome caused by mutation in ERBB3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal congenital contracture syndrome 2", "shortest_name_length": 5}
{"curie": "MONDO:0043141", "names": ["microdontia hypodontia short stature", "Microdontia hypodontia short stature", "microdontia, hypodontia, short bulbous roots and root canals with strabismus, short stature, and borderline mentality"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microdontia hypodontia short stature", "shortest_name_length": 36}
{"curie": "UMLS:C1336125", "names": ["Stage IA Squamous Cell Lung Cancer", "Stage IA Squamous Cell Lung Carcinoma", "Stage IA Squamous Cell Carcinoma of Lung", "Stage IA Squamous Cell Carcinoma of the Lung", "Stage IA Squamous Cell Lung Carcinoma AJCC v7", "Stage IA Lung Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Lung Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 34}
{"curie": "UMLS:C0854778", "names": ["Resectable Pancreatic Cancer", "Resectable Pancreas Carcinoma", "Pancreas carcinoma resectable", "Resectable Pancreatic Carcinoma", "Pancreatic carcinoma resectable", "Resectable Carcinoma of Pancreas", "Pancreatic Carcinoma, Resectable", "Resectable Carcinoma of the Pancreas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreas carcinoma resectable", "shortest_name_length": 28}
{"curie": "UMLS:C0520863", "names": ["Diastolic Dysfunction", "diastolic dysfunction", "Diastolic dysfunction", "DIASTOLIC DYSFUNCTION", "Relaxation abnormality", "Diastolic dysfunction (finding)", "diastolic dysfunction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diastolic dysfunction", "shortest_name_length": 21}
{"curie": "UMLS:C5446665", "names": ["Refractory Malignant Glomus Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Malignant Glomus Tumor", "shortest_name_length": 33}
{"curie": "MONDO:0002642", "names": ["Trochlear Nerve Tumor", "trochlear nerve tumor", "Trochlear Nerve Tumors", "trochlear nerve tumors", "tumor of Trochlear nerve", "Tumor of Trochlear Nerve", "Trochlear Nerve Neoplasm", "trochlear nerve neoplasm", "tumor of trochlear nerve", "IVth Cranial Nerve Tumors", "Trochlear Nerve Neoplasms", "IVth cranial nerve tumors", "trochlear nerve neoplasms", "Fourth Cranial Nerve Tumor", "fourth cranial nerve tumor", "fourth cranial nerve tumors", "Neoplasm of trochlear nerve", "Neoplasm of Trochlear Nerve", "neoplasm of trochlear nerve", "Fourth Cranial Nerve Tumors", "IVth Cranial Nerve Neoplasms", "tumor of the trochlear nerve", "Tumor of the Trochlear Nerve", "IVth cranial nerve neoplasms", "fourth cranial nerve neoplasm", "Tumor of Fourth Cranial Nerve", "Fourth Cranial Nerve Neoplasm", "tumor of fourth cranial nerve", "fourth cranial nerve neoplasms", "Fourth Cranial Nerve Neoplasms", "neoplasm of the trochlear nerve", "Neoplasm of the Trochlear Nerve", "neoplasm of trochlear nerve (IV)", "neoplasm of fourth cranial nerve", "Neoplasm of Fourth Cranial Nerve", "Tumor of the Fourth Cranial Nerve", "tumor of the fourth cranial nerve", "trochlear nerve neoplasm (disease)", "neoplasm of the fourth cranial nerve", "Neoplasm of the Fourth Cranial Nerve", "Neoplasm of trochlear nerve (disorder)", "neoplasm of trochlear nerve (IV) (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trochlear nerve neoplasm", "shortest_name_length": 21}
{"curie": "UMLS:C0348024", "names": ["THRYOID DYSFUNCTION", "DYSFUNCTION THYROID", "dysfunction thyroid", "thyroid dysfunction", "Dysfunction thyroid", "Thyroid dysfunction", "dysfunction; thyroid", "Thyroid dysfunction (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid dysfunction", "shortest_name_length": 19}
{"curie": "UMLS:C0235762", "names": ["Rheumatoid arthritis aggravated", "Arthritis rheumatoid aggravated", "ARTHRITIS RHEUMATOID AGGRAVATED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arthritis rheumatoid aggravated", "shortest_name_length": 31}
{"curie": "UMLS:C5556513", "names": ["Mixed Trophoblastic Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mixed Trophoblastic Tumor", "shortest_name_length": 25}
{"curie": "UMLS:C5420335", "names": ["Parotid Gland Sialolipoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parotid Gland Sialolipoma", "shortest_name_length": 25}
{"curie": "MONDO:0002811", "names": ["Ca main bronchus", "main bronchus cancer", "cancer of main bronchus", "malignant tumor of main bronchus", "malignant main bronchus neoplasm", "Malignant neoplasm of main bronchus", "malignant neoplasm of main bronchus", "Malignant Neoplasm of Main Bronchus", "Malignant neoplasm of main bronchus (disorder)", "malignant neoplasm of main bronchus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "main bronchus cancer", "shortest_name_length": 16}
{"curie": "UMLS:C3489572", "names": ["Idiopathic Extrahepatic Biliary Atresia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Idiopathic Extrahepatic Biliary Atresia", "shortest_name_length": 39}
{"curie": "MONDO:0011644", "names": ["par planitis", "Pars Planitis", "pars planitis", "Pars planitis", "PARS PLANITIS", "Planitis, Pars", "posterior cyclitis", "Posterior cyclitis", "cyclitis; posterior", "posterior; cyclitis", "Pars planitis (disorder)", "Posterior cyclitis (disorder)", "chorioretinitis pars planitis", "pars plana of ciliary bodyitis", "peripheral retinal inflammation", "familial pars planitis (subtype)", "pars plana of ciliary body inflammation", "chorioretinitis pars planitis (diagnosis)", "inflammation of pars plana of ciliary body"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pars planitis", "shortest_name_length": 12}
{"curie": "UMLS:C0156353", "names": ["prolapse uterovaginal", "Uterovaginal prolapse", "uterovaginal prolapse", "UTEROVAGINAL PROLAPSE", "uterovaginal; prolapse", "prolapse; uterovaginal", "Uterovaginal prolapse, NOS", "Vaginal and cervical prolapse", "Vaginal AND cervical prolapse", "Uterovaginal prolapse (disorder)", "uterovaginal prolapse (diagnosis)", "Uterovaginal prolapse, unspecified", "uterovaginal prolapse (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterovaginal prolapse", "shortest_name_length": 21}
{"curie": "MONDO:0700016", "names": ["chromosome 9 disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 9 disorder", "shortest_name_length": 21}
{"curie": "MONDO:0021240", "names": ["tumor tongue", "tongue tumor", "Tongue Tumor", "tongue tumors", "Tumor of Tongue", "tumor of tongue", "Tongue Neoplasm", "Tongue neoplasm", "neoplasm tongue", "tongue neoplasm", "of tongue tumor", "Tumor of tongue", "Neoplasm, Tongue", "tongue neoplasms", "Tumour of tongue", "neoplasms tongue", "Tongue Neoplasms", "Neoplasms, Tongue", "neoplasm of tongue", "Neoplasm of Tongue", "Neoplasm of tongue", "tumor of the tongue", "Tongue neoplasm NOS", "Tumor of the Tongue", "Neoplasm of the Tongue", "neoplasm of the tongue", "Neoplasm of the tongue", "tongue neoplasm (disease)", "Neoplasm of tongue (disorder)", "neoplasm of tongue (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tongue neoplasm", "shortest_name_length": 12}
{"curie": "MONDO:0004992", "names": ["MT", "CA", "Cancer", "CANCER", "cancer", "Cancers", "^Cancer", "cancers", "Blastoma", "malignancy", "Cancer NOS", "Malignancy", "MALIGNANCY", "CA - Cancer", "cancer, NOS", "CANCER (NOS)", "Malignancies", "malignancies", "Cancer (NOS)", "MALIGNANCIES", "Neoplasm Site", "neoplasm site", "Site, Neoplasm", "primary cancer", "Neoplasm Sites", "Malignancy nos", "malignant tumor", "Malignant Tumor", "neoplasm/cancer", "MALIGNANT TUMOR", "Sites, Neoplasm", "Malignant tumor", "cell type cancer", "Malignant Growth", "malignant tumour", "malignant tumors", "Neoplasm by Site", "Malignant tumour", "malignant Growth", "Tumor, malignant", "malignant tumours", "Tumour, malignant", "Neoplasms by Site", "neoplasm location", "malignant neoplasm", "cancer (diagnosis)", "Malignant Neoplasm", "NEOPLASM MALIGNANT", "Malignant neoplasm", "Neoplasms by Sites", "Neoplasm malignant", "Malignant neoplasms", "Malignant Neoplasms", "organ system cancer", "NEOPLASM, MALIGNANT", "Neoplasm, malignant", "neoplasm, malignant", "Neoplasm, Malignant", "malignant neoplasms", "Neoplasms, Malignant", "Tumor, malignant, NOS", "Malignant neoplasm NOS", "Cancer, unspecified site", "malignant tumoral disease", "Malignancy, unspecified site", "Unclassified malignant tumor", "Malignant Neoplastic Disease", "Malignant neoplastic disease", "malignant neoplastic disease", "malignant neoplasm (disease)", "neoplasm (disease), malignant", "Unclassified tumor, malignant", "Unclassified malignant tumour", "Neoplastic disease, malignant", "Malignant neoplasm morphology", "tumor; malignant, unclassified", "malignant neoplasm (diagnosis)", "tumor; unclassified, malignant", "Unclassified tumour, malignant", "Malignant neoplastic disease (disorder)", "Malignant neoplasm (morphologic abnormality)", "Malignant neoplasm without specification of site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cancer", "shortest_name_length": 2}
{"curie": "MONDO:0015204", "names": ["microlissencephaly", "Microlissencephaly", "Microlissencephalies", "Type 3 lissencephaly", "Type III lissencephaly", "Lissencephaly type III", "Microlissencephaly (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microlissencephaly", "shortest_name_length": 18}
{"curie": "MONDO:0016841", "names": ["Del(20)(p12.3)", "monosomy 20p12.3", "Monosomy 20p12.3", "20p12.3 microdeletion syndrome", "20p12.3 microdeletion syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "20p12.3 microdeletion syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C1136041", "names": ["Familial Acoustic Neuroma", "Familial Acoustic Neuromas", "Neuroma, Familial Acoustic", "Acoustic Neuroma, Familial", "Acoustic Neuromas, Familial", "Neuromas, Familial Acoustic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Familial Acoustic Neuroma", "shortest_name_length": 25}
{"curie": "UMLS:C1336368", "names": ["Stage IVB Extrahepatic Bile Duct Cancer", "Extrahepatic Bile Duct Cancer Stage IVB", "Stage IVB Extrahepatic Bile Duct Carcinoma", "Stage IVB Carcinoma of Extrahepatic Bile Duct", "Stage IVB Carcinoma of the Extrahepatic Bile Duct"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Extrahepatic Bile Duct Cancer", "shortest_name_length": 39}
{"curie": "MONDO:0007621", "names": ["FHS", "FLHS", "floating-harbor syndrome", "floating-HARBOR syndrome", "floating-Harbor syndrome", "floating harbor syndrome", "Floating-Harbor syndrome", "Floating-harbor syndrome", "Floating-Harbor Syndrome", "FLOATING-HARBOR SYNDROME", "Pelletier-Leisti syndrome", "Floating-Harbour syndrome", "floating harbour syndrome", "floating-harbour syndrome", "Floating-Harbor syndrome (FHS)", "Leisti-Hollander-Rimoin Syndrome", "Floating-Harbor syndrome (disorder)", "Floating-Harbor syndrome (diagnosis)", "inherited genetic conditions autosomal dominant Floating-Harbor syndrome", "short stature with delayed bone age, expressive language delay, a triangular face with a prominent nose and deep-set eyes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Floating-Harbor syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0035407", "names": ["furuncular myiasis due to Cordylobia anthropophaga", "furunculous myiasis due to Cordylobia anthropophaga", "furunculoid myiasis due to Cordylobia anthropophaga"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "furuncular myiasis due to Cordylobia anthropophaga", "shortest_name_length": 50}
{"curie": "MONDO:0017904", "names": ["Lyngstadaas syndrome", "steroid dehydrogenase deficiency dental anomalies", "Steroid dehydrogenase deficiency dental anomalies", "Steroid dehydrogenase deficiency-dental anomalies syndrome", "steroid dehydrogenase deficiency-dental anomalies syndrome", "Steroid dehydrogenase deficiency and dental anomaly syndrome", "severe dental aberrations in familial steroid dehydrogenase deficiency", "Steroid dehydrogenase deficiency and dental anomaly syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "steroid dehydrogenase deficiency-dental anomalies syndrome", "shortest_name_length": 20}
{"curie": "UMLS:C1959799", "names": ["Calcium renal calculus", "Calcium renal calculus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Calcium renal calculus", "shortest_name_length": 22}
{"curie": "MONDO:0014804", "names": ["SIDBA3", "sideroblastic anemia 3", "GLRX5-related sideroblastic anemia", "anemia, sideroblastic, 3, pyridoxine-refractory", "ANEMIA, SIDEROBLASTIC, 3, PYRIDOXINE-REFRACTORY", "GLRX5 (glutaredoxin 5) related sideroblastic anemia", "adult-onset autosomal recessive sideroblastic anemia", "Adult-onset autosomal recessive sideroblastic anemia", "GLRX5 (glutaredoxin 5) related sideroblastic anaemia", "Adult-onset autosomal recessive sideroblastic anaemia", "Adult-onset autosomal recessive sideroblastic anemia (disorder)", "autosomal recessive pyridoxine-refractory sideroblastic anemia 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sideroblastic anemia 3", "shortest_name_length": 6}
{"curie": "MONDO:0018096", "names": ["WMS", "Marchesani", "WM syndrome", "GEMSS syndrome", "Weill-Marchesani", "Marchesani Syndrome", "marchesani syndrome", "Marchesani's syndrome", "Marchesani-Weill Syndrome", "Weill Marchesani Syndrome", "weill-marchesani syndrome", "Marchesani-Weill syndrome", "Marchesani Weill Syndrome", "Weill-Marchesani Syndrome", "Weill-Marchesani syndrome", "Marchesani-Weill Syndromes", "congenital mesodermal dystrophy", "Brachydactyly-spherophakia syndrome", "Spherophakia-Brachymorphia Syndrome", "Spherophakia-brachymorphia syndrome", "spherophakia brachymorphia syndrome", "spherophakia-brachymorphia syndrome", "Spherophakia Brachymorphia Syndrome", "Weill-Marchesani syndrome (disorder)", "Spherophakia Brachymorphia Syndromes", "Syndrome, Spherophakia Brachymorphia", "Weill-Marchesani syndrome (diagnosis)", "Syndromes, Spherophakia Brachymorphia", "Brachymorphy with spherophakia syndrome", "Congenital Mesodermal Dysmorphodystrophy", "mesodermal dysmorphodystrophy congenital", "Mesodermal Dysmorphodystrophy, Congenital", "Dysmorphodystrophy, Congenital Mesodermal", "mesodermal Dysmorphodystrophy, congenital", "Congenital Mesodermal Dysmorphodystrophies", "Dysmorphodystrophies, Congenital Mesodermal", "Mesodermal Dysmorphodystrophies, Congenital"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Weill-Marchesani syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0006055", "names": ["sex cord tumor", "Sex cord tumor", "cord sex tumors", "sex cord neoplasm", "tumor of sex cord", "Sex cord tumor, NOS", "neoplasm of sex cord", "Sex cord tumour, NOS", "gonadal stromal tumor", "Gonadal stromal tumor", "sex cord-stromal tumor", "Sex Cord Stromal Tumor", "sex cord stromal tumor", "Sex Cord-Stromal Tumor", "Sex cord stromal tumor", "Sex cord-stromal tumor", "Gonadal stromal tumour", "Sex cord stromal tumour", "Sex cord-stromal tumour", "cord sex stromal tumors", "Tumor, Sex Cord-Stromal", "Sex Cord-Stromal Tumors", "Tumors, Sex Cord-Stromal", "Specialized gonadal tumor", "Sex cord-stromal neoplasm", "Sex Cord-Stromal neoplasm", "Sex Cord-Stromal Neoplasm", "specialized gonadal tumor", "Specialised gonadal tumour", "Gonadal stromal tumor, NOS", "Specialized gonadal tumour", "Specialised gonadal neoplasm", "specialized gonadal neoplasm", "Specialized gonadal neoplasm", "Specialized Gonadal Neoplasms", "SPECIALIZED GONADAL NEOPLASMS", "sex cord-gonadal stromal tumor", "Sex Cord-Gonadal Stromal Tumors", "sex cord-gonadal stromal tumour", "Sex cord-stromal tumor, no ICD-O subtype", "Malignant Testicular Sex Cord-Stromal Tumor", "specialized gonadal tumor (qualifier value)", "malignant testicular sex cord-stromal tumor", "specialized gonadal neoplasm (morphologic abnormality)", "Specialized gonadal neoplasm (morphologic abnormality)", "specialized gonadal neoplasm NOS (morphologic abnormality)", "Sex cord-stromal tumor, no ICD-O subtype (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sex cord-stromal tumor", "shortest_name_length": 14}
{"curie": "MONDO:0010637", "names": ["KFSDX", "Kfsdx", "keratosis follicularis spinulosa decalvans", "Keratosis follicularis spinulosa decalvans", "X-linked keratosis follicularis spinulosa decalvans", "Keratosis Follicularis Spinulosa Decalvans, X-Linked", "keratosis follicularis spinulosa decalvans, X-linked", "keratosis follicularis SPINULOSA decalvans, X-linked", "KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED", "keratosis follicularis Spinulosa decalvans cum Ophiasi", "Keratosis follicularis spinulosa decalvans cum ophiasi", "keratosis follicularis spinulosa decalvans cum ophiasi", "KERATOSIS FOLLICULARIS SPINULOSA DECALVANS CUM OPHIASI", "keratosis follicularis spinulosa decalvans, X-linked, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratosis follicularis spinulosa decalvans, X-linked", "shortest_name_length": 5}
{"curie": "UMLS:C0861355", "names": ["Recurrent Breast Adenocarcinoma", "Breast adenocarcinoma recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast adenocarcinoma recurrent", "shortest_name_length": 31}
{"curie": "UMLS:C0920269", "names": ["MSI", "MSI Present", "MSI Positive", "Microsatellite Instability", "instability microsatellite", "microsatellite instability", "Instability, Microsatellite", "Microsatellite Instability Present", "Microsatellite Instability Positive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Microsatellite Instability", "shortest_name_length": 3}
{"curie": "UMLS:C2981375", "names": ["Stage IIIA Esophageal Squamous Cell Cancer", "Stage IIIA Esophageal Squamous Cell Carcinoma", "Stage IIIA Esophageal Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Esophageal Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 42}
{"curie": "MONDO:0004177", "names": ["neoplasm. urethra", "neoplasm of urethra", "Benign Urethra Tumor", "benign urethra tumor", "Benign urethral tumor", "benign urethral tumor", "Benign Urethral Tumor", "Benign urethral tumour", "Benign Urethra Neoplasm", "Benign tumor of urethra", "benign urethra neoplasm", "urethra benign neoplasm", "benign tumor of urethra", "Benign Tumor of Urethra", "Neoplasm benign;urethra", "urethral benign neoplasm", "benign urethral neoplasm", "Benign Urethral Neoplasm", "Benign tumour of urethra", "Benign neoplasm of urethra", "benign neoplasm of urethra", "Benign Neoplasm of Urethra", "benign tumor of the urethra", "Benign Tumor of the Urethra", "Benign Urethral Neoplasm NOS", "Benign urethral neoplasm NOS", "Benign Neoplasm of the Urethra", "benign neoplasm of the urethra", "Benign neoplasm of urethra (disorder)", "benign neoplasm of urethra (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign urethral neoplasm", "shortest_name_length": 17}
{"curie": "MONDO:0006789", "names": ["Hyperamylasemia", "HYPERAMYLASEMIA", "hyperamylasemia", "Elevated Amylase", "Hyperamylasaemia", "hyperamylasemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperamylasemia", "shortest_name_length": 15}
{"curie": "MONDO:0007133", "names": ["Kumar Levick syndrome", "Kumar-Levick syndrome", "Anonychia-onychodystrophy with brachydactyly type B and ectrodactyly", "ANONYCHIA-ONYCHODYSTROPHY WITH BRACHYDACTYLY TYPE B AND ECTRODACTYLY", "anonychia-onychodystrophy with brachydactyly type b and ectrodactyly", "autosomal dominant onychodystrophy and anonychia with type B brachydactyly and ectrodactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anonychia-onychodystrophy with brachydactyly type b and ectrodactyly", "shortest_name_length": 21}
{"curie": "MONDO:0014529", "names": ["CFDS", "CEREBELLOFACIODENTAL syndrome", "Cerebellofaciodental syndrome", "CEREBELLOFACIODENTAL SYNDROME", "cerebellofaciodental syndrome", "cerebellar-facial-dental syndrome", "CEREBELLAR-FACIAL-DENTAL SYNDROME", "Cerebellar-facial-dental syndrome", "Cerebellar-facial-dental syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellar-facial-dental syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0036511", "names": ["childhood kidney cancer", "pediatric kidney cancer", "kidney cancer of childhood", "childhood malignant renal tumor", "Childhood Malignant Renal Tumor", "Childhood Malignant Kidney Tumor", "childhood malignant kidney tumor", "childhood malignant renal neoplasm", "Childhood Malignant Renal Neoplasm", "Childhood Malignant Kidney Neoplasm", "childhood malignant kidney neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood malignant kidney neoplasm", "shortest_name_length": 23}
{"curie": "UMLS:C4552929", "names": ["Stage IC Ovarian Cancer", "Stage IC Ovarian Cancer AJCC v8", "Stage IC Ovarian Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IC Ovarian Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "UMLS:C0278080", "names": ["Physical addiction", "physical addiction", "Physical Dependence", "physical dependence", "Addiction, physical", "physiological addiction", "Physiological addiction", "physical AOD dependence", "physiological dependence", "DEPENDENCE PHYSIOLOGICAL", "Dependence physiological", "biological AOD dependence", "physiological AOD dependence", "Physical addiction (finding)", "physical Alcohol or Other Drugs dependence", "biological alcohol or other drug dependence", "biological Alcohol or Other Drugs dependence", "physiological Alcohol or Other Drugs dependence"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Physical addiction", "shortest_name_length": 18}
{"curie": "MONDO:0004360", "names": ["breast osteosarcoma", "Breast Osteosarcoma", "Osteosarcoma of Breast", "osteosarcoma of breast", "osteogenic breast sarcoma", "Osteogenic Breast Sarcoma", "osteosarcoma of the breast", "Osteosarcoma of the Breast", "Osteogenic Sarcoma of Breast", "Osteogenic sarcoma of breast", "osteogenic sarcoma of breast", "breast osteosarcoma (disease)", "Osteogenic Sarcoma of the Breast", "osteogenic sarcoma of the breast", "Breast Extraskeletal Osteosarcoma", "breast extraskeletal osteosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast extraskeletal osteosarcoma", "shortest_name_length": 19}
{"curie": "UMLS:C0271178", "names": ["Irvine's syndrome", "Irvine-Gass Syndrome", "Irvine-Gass syndrome", "Irvine Gass Syndrome", "Syndrome, Irvine-Gass", "Vitreous tug syndrome", "Irvine-Glass syndrome", "Postoperative cataract syndrome", "Postoperative cystoid macular edema", "cystoid macular edema postoperative", "Postoperative cystoid macular oedema", "Cystoid Macular Edema, Postoperative", "Postoperative cataract syndrome (disorder)", "Visual impairment, post-operative, cataract", "Postoperative cystoid macular edema (disorder)", "Postoperative cystoid macular edema (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Irvine-Gass Syndrome", "shortest_name_length": 17}
{"curie": "MONDO:0002757", "names": ["acute allergic sanguinous otitis media", "Acute allergic sanguinous otitis media", "Acute allergic sanguinous otitis media (disorder)", "acute allergic sanguinous otitis media (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute allergic sanguinous otitis media", "shortest_name_length": 38}
{"curie": "UMLS:C5205057", "names": ["Recurrent Diffuse Large B-Cell Lymphoma Germinal Center B-Cell Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Diffuse Large B-Cell Lymphoma Germinal Center B-Cell Type", "shortest_name_length": 67}
{"curie": "UMLS:C4526898", "names": ["Soft Tissue Sarcoma Trunk and Extremities by AJCC v8 Stage", "Soft Tissue Sarcoma of the Trunk and Extremities by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Soft Tissue Sarcoma of the Trunk and Extremities by AJCC v8 Stage", "shortest_name_length": 58}
{"curie": "MONDO:0004066", "names": ["Intermediate Cell Type Ciliary Body Melanoma", "Intermediate cell type ciliary body melanoma", "intermediate cell type ciliary body melanoma", "Ciliary Body Intermediate Cell Type Melanoma", "ciliary body intermediate cell type uveal melanoma", "intermediate cell type uveal melanoma of ciliary body"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intermediate cell type ciliary body melanoma", "shortest_name_length": 44}
{"curie": "MONDO:0006356", "names": ["Parotid Adenoid Cystic Carcinoma", "parotid adenoid cystic carcinoma", "adenoid cystic carcinoma of parotid", "Adenoid Cystic Carcinoma of Parotid", "parotid gland adenoid cystic carcinoma", "Parotid Gland Adenoid Cystic Carcinoma", "adenoid cystic carcinoma of the parotid", "Adenoid Cystic Carcinoma of the Parotid", "Adenoid cystic carcinoma of parotid gland", "adenoid cystic carcinoma of parotid gland", "Adenoid Cystic Carcinoma of Parotid Gland", "adenoid cystic carcinoma of the parotid gland", "Adenoid Cystic Carcinoma of the Parotid Gland", "malignant parotid neoplasm carcinoma adenoid cystic", "Adenoid cystic carcinoma of parotid gland (disorder)", "Adenoid cystic carcinoma of parotid gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parotid gland adenoid cystic carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0012104", "names": ["APLD", "Simons", "Barraquer", "Simons' disease", "SIMONS SYNDROME", "Simons' syndrome", "Barraquer syndrome", "Partial lipoatrophy", "Lipodystrophy, partial", "APLD, susceptibility to", "BARRAQUER-SIMONS DISEASE", "Barraquer-Simons disease", "Hollander-Simons syndrome", "Barraquer-Simons Syndrome", "Progressive lipodystrophy", "HOLLAENDER-SIMONS DISEASE", "Barraquer-Simons syndrome", "progressive lipodystrophy", "LIPODYSTROPHY, PROGRESSIVE", "Acquired Partial Lipodystrophy", "Acquired partial lipodystrophy", "acquired partial lipodystrophy", "partial acquired lipodystrophy", "lipodystrophy partial acquired", "Lipodystrophy, Partial, Acquired", "lipodystophy partial progressive", "Progressive partial lipodystrophy", "Progressive lipodystrophy disease", "lipodystrophy cephalothoracic type", "Lipodystrophy, Cephalothoracic Type", "lipodystrophy, cephalothoracic type", "lipodystrophy, partial, progressive", "Lipodystrophy, Partial, Progressive", "Barraquer-Simons disease (diagnosis)", "progressive lipodystrophy (diagnosis)", "Macrodystrophia lipomatosa progressiva", "Acquired partial lipodystrophy (disorder)", "progressive cephalothoracic lipodystrophy", "Progressive cephalothoracic lipodystrophy", "Lipodystrophic diabetes with partial lipoatrophy", "susceptibility to partial acquired lipodystrophy", "lipodystrophy, partial, acquired, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired partial lipodystrophy", "shortest_name_length": 4}
{"curie": "MONDO:0003702", "names": ["uterus intravenous leiomyomatosis", "uterus intravascular leiomyomatosis", "Intravenous Leiomyomatosis of Uterus", "intravenous leiomyomatosis of uterus", "Intravascular Leiomyomatosis of Uterus", "intravascular leiomyomatosis of uterus", "Intravascular leiomyomatosis of Uterus", "intravenous leiomyomatosis of the uterus", "Intravenous Leiomyomatosis of the Uterus", "uterine corpus intravenous leiomyomatosis", "Uterine Corpus Intravenous Leiomyomatosis", "Intravascular Leiomyomatosis of the Uterus", "intravascular leiomyomatosis of the uterus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterus intravascular leiomyomatosis", "shortest_name_length": 33}
{"curie": "MONDO:0024422", "names": ["auditory inattention", "inattention, auditory", "auditory Inattentions", "Inattentions, auditory", "Psychoacoustical Disorder", "auditory disorder process", "Psychoacoustical disorder", "disorder, Psychoacoustical", "Psychoacoustical Disorders", "auditory disorders process", "Psychoacoustical disorders", "Disorder, Psychoacoustical", "disorders, Psychoacoustical", "Disorders, Psychoacoustical", "acoustic perceptual disorder", "Auditory Processing Disorder", "Acoustic Perceptual Disorder", "auditory disorder processing", "Auditory Perceptual Disorder", "auditory perceptual disorder", "auditory processing disorder", "Auditory processing disorder", "processing auditory disorder", "processing disorder, auditory", "auditory perceptual disorders", "perceptual disorder, auditory", "acoustic perceptual disorders", "Perceptual Disorder, Auditory", "Disorder, Acoustic Perceptual", "Auditory Perceptual Disorders", "disorder, auditory processing", "disorder, acoustic perceptual", "Disorder, Auditory Processing", "Processing Disorder, Auditory", "Acoustic Perceptual Disorders", "Auditory Processing Disorders", "auditory processing disorders", "Perceptual Disorder, Acoustic", "perceptual disorder, acoustic", "disorders, auditory processing", "perceptual disorders, acoustic", "processing disorders, auditory", "perceptual disorders, auditory", "Perceptual Disorders, Auditory", "Disorders, Acoustic Perceptual", "Disorders, Auditory Processing", "disorders, acoustic perceptual", "Processing Disorders, Auditory", "Perceptual Disorders, Acoustic", "Auditory Comprehension Disorder", "auditory comprehension disorder", "comprehension disorder, auditory", "Auditory processing disorder NOS", "auditory comprehension disorders", "Disorder, Auditory Comprehension", "Auditory Comprehension Disorders", "disorder, auditory comprehension", "Comprehension Disorder, Auditory", "comprehension disorders, auditory", "Comprehension Disorders, Auditory", "disorders, auditory comprehension", "Disorders, Auditory Comprehension", "sensory perception of sound disease", "Central Auditory Processing Disorder", "Central auditory processing disorder", "central auditory processing disorder", "Auditory Processing Disorder, Central", "disorder of sensory perception of sound", "Auditory processing disorder (disorder)", "Central auditory processing disorder (disorder)", "central auditory processing disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "auditory perceptual disorders", "shortest_name_length": 20}
{"curie": "MONDO:0007337", "names": ["syngnathia", "Syngnathia", "SYNGNATHIA", "CPLS Syndrome", "CPLS syndrome", "Cpls syndrome", "CPLS SYNDROME", "Cleft palate lateral synechia syndrome", "Cleft palate-lateral synechia syndrome", "CLEFT PALATE-LATERAL SYNECHIA SYNDROME", "Cleft Palate-Lateral Synechia Syndrome", "cleft palate lateral synechia syndrome", "cleft palate-lateral synechia syndrome", "cleft palate-lateral synechiae syndrome", "CPLS - cleft palate-lateral synechia syndrome", "cleft palate-lateral synechiae (CPLS) syndrome", "Cleft palate lateral synechia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleft palate-lateral synechia syndrome", "shortest_name_length": 10}
{"curie": "UMLS:C0851401", "names": ["Maternal Disorder", "Maternal Pregnancy Complication", "Maternal Complication of Pregnancy", "Maternal complications of pregnancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Maternal complications of pregnancy", "shortest_name_length": 17}
{"curie": "MONDO:0005909", "names": ["Pestivirus infection", "Pestivirus Infection", "Pestivirus infections", "Infection, Pestivirus", "infection, Pestivirus", "Pestivirus Infections", "infections, Pestivirus", "Infections, Pestivirus", "Disease due to Pestivirus", "DISEASES DUE TO PESTIVIRUS", "pestivirus infectious disease", "Pestivirus infectious disease", "Pestivirus disease or disorder", "Disease due to Pestivirus, NOS", "Disease due to Pestivirus (disorder)", "Pestivirus caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pestivirus infectious disease", "shortest_name_length": 20}
{"curie": "MONDO:0037937", "names": ["pyrimidine metabolism disease", "metabolic disorder; pyrimidine", "pyrimidine; metabolic disorder", "pyrimidine metabolism disorder", "Disorder of pyrimidine metabolism", "disorder of pyrimidine metabolism", "DISORDERS OF PYRIMIDINE METABOLISM", "Disorders of pyrimidine metabolism", "Disorder of pyrimidine metabolism, NOS", "Disorder of pyrimidine metabolism (disorder)", "pyrimidine nucleobase metabolic process disease", "disorder of pyrimidine nucleobase metabolic process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyrimidine metabolism disease", "shortest_name_length": 29}
{"curie": "UMLS:C0278748", "names": ["Regional GI Carcinoid Tumor", "Regional Digestive Carcinoid Tumor", "regional gastrointestinal carcinoid tumor", "Regional Gastrointestinal Carcinoid Tumor", "gastrointestinal carcinoid tumor, regional", "Regional Gastrointestinal Neuroendocrine Tumor G1", "Regional Digestive System Neuroendocrine Tumor G1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Regional Digestive System Neuroendocrine Tumor G1", "shortest_name_length": 27}
{"curie": "MONDO:0036192", "names": ["ENDOVES", "ENDOVE syndrome", "EN1-related dorsoventral syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "EN1-related dorsoventral syndrome", "shortest_name_length": 7}
{"curie": "UMLS:C4054368", "names": ["Nephrotic Syndrome - Relapse"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - Relapse", "shortest_name_length": 28}
{"curie": "MONDO:0013869", "names": ["APRTD", "APRT DEFICIENCY", "APRT deficiency", "APRT Deficiency", "urolithiasis, Dha", "UROLITHIASIS, DHA", "Dihydroxyadeninuria", "nephrolithiasis, Dha", "NEPHROLITHIASIS, DHA", "2,8-Dihydroxyadeninuria", "DHA Crystalline Nephropathy", "2,8-dihydroxyadeninuria disease", "Deficiency of AMP pyrophorylase", "2,8-Dihydroxyadenine Urolithiasis", "2,8-dihydroxyadenine urolithiasis", "2,8-Dihydroxyadenine urolithiasis", "UROLITHIASIS, 2,8-DIHYDROXYADENINE", "urolithiasis, 2,8-dihydroxyadenine", "Urolithiasis, 2,8-Dihydroxyadenine", "adenine phosphoribosyltransferase deficiency", "Adenine phosphoribosyltransferase deficiency", "ADENINE PHOSPHORIBOSYLTRANSFERASE DEFICIENCY", "Adenine Phosphoribosyltransferase Deficiency", "Adenine phosphoribosyl transferase deficiency", "deficiency of adenine phosphoribosyltransferase", "Deficiency of adenine phosphoribosyltransferase", "Deficiency of adenine phosphoribosyltransferase (disorder)", "deficiency of adenine phosphoribosyltransferase (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenine phosphoribosyltransferase deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0004385", "names": ["adult xanthogranuloma", "Adult Xanthogranuloma", "xanthogranuloma of adults"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult xanthogranuloma", "shortest_name_length": 21}
{"curie": "UMLS:C5206669", "names": ["Penile Neurofibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Penile Neurofibroma", "shortest_name_length": 19}
{"curie": "UMLS:C3897245", "names": ["Undifferentiated JIA", "Undifferentiated Juvenile Idiopathic Arthritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Undifferentiated Juvenile Idiopathic Arthritis", "shortest_name_length": 20}
{"curie": "MONDO:0002617", "names": ["bone angiosarcoma", "Bone Angiosarcoma", "bone hemangiosarcoma", "Bone Hemangiosarcoma", "Osseous Angiosarcoma", "osseous angiosarcoma", "angiosarcoma of bone", "hemangiosarcoma of bone", "Osseous Hemangiosarcoma", "osseous hemangiosarcoma", "Bone Angioendothelial Sarcoma", "bone angioendothelial sarcoma", "osseous angioendothelial sarcoma", "angiosarcoma of bone (diagnosis)", "bone Hemangioendothelial sarcoma", "Bone Hemangioendothelial Sarcoma", "Osseous Angioendothelial Sarcoma", "bone tissue angiosarcoma (disease)", "hemangioendothelial sarcoma of bone", "hemangiosarcoma of bone (diagnosis)", "angiosarcoma (disease) of bone tissue", "hemangioendothelial sarcoma of bone (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bone angiosarcoma", "shortest_name_length": 17}
{"curie": "MONDO:0002150", "names": ["disease hypothalamic", "hypothalamic disease", "Hypothalamic Disease", "hypothalamus disease", "Hypothalamic disease", "hypothalamic disorder", "Hypothalamic disorder", "disorder hypothalamic", "hypothalamus disorder", "disorder hypothalamus", "hypothalamic diseases", "Hypothalamic Diseases", "Disease, Hypothalamic", "Hypothalamus disorder", "disorders hypothalamic", "Diseases, Hypothalamic", "disorders hypothalamus", "disease of hypothalamus", "Disorder of hypothalamus", "disorder of hypothalamus", "hypothalamus disease or disorder", "disease or disorder of hypothalamus", "Disorder of hypothalamus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypothalamic disorder", "shortest_name_length": 20}
{"curie": "MONDO:0006566", "names": ["keratoses", "Keratosis", "Keratoses", "KERATOSIS", "keratosis", "keratoderma", "Keratoderma", "KERATODERMA", "keratodermia", "keratodermas", "Keratosis, NOS", "Hyperkeratosis", "Keratosis (disorder)", "Dermal hyperkeratosis", "Keratoderma (disorder)", "Hyperkeratosis of skin", "keratoderma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratosis", "shortest_name_length": 9}
{"curie": "MONDO:0018039", "names": ["SIgMD", "selective IgM deficiency", "Selective IgM deficiency", "Selective IgM Immunodeficiency", "Selective IgM immunodeficiency", "selective IgM deficiency disease", "selective IgM deficiency (diagnosis)", "selective immunoglobulin M deficiency", "Selective immunoglobulin M deficiency", "immunoglobulin; deficiency IgM selective", "Selective deficiency of immunoglobulin M [IgM]", "Selective immunoglobulin M deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "selective IgM deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C0857808", "names": ["In Utero Drug Exposure", "Drug exposure in utero"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drug exposure in utero", "shortest_name_length": 22}
{"curie": "UMLS:C0153878", "names": ["CLL in Remission", "CLL in remission", "Chronic lymphoid leukemia in remission", "Chronic Lymphoid Leukemia in Remission", "Chronic lymphoid leukaemia in remission", "Chronic lymphoid leukemia, in remission", "Chronic Lymphocytic Leukemia in Remission", "chronic lymphocytic leukemia in remission", "Chronic Lymphogenous Leukemia in Remission", "Chronic lymphocytic leukemia, in remission", "Chronic lymphocytic leukaemia, in remission", "Chronic lymphocytic leukemia (in remission)", "Chronic Lymphocytic Leukemia (in Remission)", "Chronic lymphocytic leukaemia (in remission)", "Chronic Lymphocytic Leukemia (CLL) in Remission", "leukemia lymphocytic chronic (CLL) in remission", "Chronic lymphoid leukemia in remission (disorder)", "chronic lymphocytic leukemia in remission (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic lymphoid leukemia in remission", "shortest_name_length": 16}
{"curie": "UMLS:C0521170", "names": ["Low-Trauma Fracture", "Osteoporotic Fracture", "Fracture;osteoporotic", "osteoporotic fracture", "fracture osteoporosis", "Osteoporotic fracture", "Osteoporosis fracture", "OSTEOPOROSIS FRACTURE", "osteoporosis fracture", "fractures osteoporosis", "Osteoporotic Fractures", "Fracture, Osteoporotic", "fractures osteoporotic", "Fractures, Osteoporotic", "OSTEOPOROSIS WITH FRACTURE", "due fractures osteoporosis", "Osteoporosis with fracture", "FRACTURE DUE TO OSTEOPOROSIS", "Fracture due to osteoporosis", "Osteoporotic fracture of bone", "pathological fracture; osteoporosis", "Osteoporosis with pathological fracture", "Osteoporotic fracture of bone (disorder)", "osteoporosis; with pathological fracture", "fracture; pathological, with osteoporosis", "Osteoporotic fracture (morphologic abnormality)", "Unspecified osteoporosis with pathological fracture"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Osteoporotic Fractures", "shortest_name_length": 19}
{"curie": "UMLS:C3274463", "names": ["S Beta 0 Thalassemia", "Hb S Beta 0 Thalassemia", "Sickle Beta 0 Thalassemia", "Sickle Beta Zero Thalassemia", "Hemoglobin S Beta 0 Thalassemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sickle Beta 0 Thalassemia", "shortest_name_length": 20}
{"curie": "MONDO:0003758", "names": ["Testicular Germ Cell Tumor", "testicular germ cell tumor", "Pediatric Testicular Germ Cell Tumor", "childhood testicular germ cell tumor", "pediatric testicular germ cell tumor", "Childhood Testicular Germ Cell Tumor", "paediatric testicular germ cell tumour", "childhood testicular germ cell neoplasm", "pediatric testicular germ cell neoplasm", "Pediatric Testicular Germ Cell Neoplasm", "Childhood Testicular Germ Cell Neoplasm", "testicular germ cell tumor of childhood", "paediatric testicular germ cell neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood testicular germ cell tumor", "shortest_name_length": 26}
{"curie": "MONDO:0003002", "names": ["dysgerminoma", "Dysgerminoma", "disgerminoma", "Disgerminoma", "dysgerminomas", "Dysgerminomas", "Disgerminomas", "dysgerminoma (disease)", "Malignant dysgerminoma", "DYSGERMINOMA, MALIGNANT", "dysgerminoma, malignant", "dysgerminoma (diagnosis)", "Malignant dysgerminoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dysgerminoma", "shortest_name_length": 12}
{"curie": "UMLS:C0342114", "names": ["goiter diffuse", "GOITER DIFFUSE", "Goiter diffuse", "Diffuse goitre", "Goitre diffuse", "Diffuse goiter", "diffuse goiter", "Diffuse Goiter", "diffuse goitre", "Nontoxic diffuse goitre", "Nontoxic diffuse goiter", "diffuse nontoxic goiter", "Non-toxic diffuse goiter", "Non-toxic diffuse goitre", "Diffuse goiter (disorder)", "diffuse nontoxic goiter (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse goiter", "shortest_name_length": 14}
{"curie": "MONDO:0017733", "names": ["alpha-mannosidosis, adult form", "Alpha-mannosidosis adult-onset form", "lysosomal alpha-D-mannosidase deficiency, adult form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alpha-mannosidosis, adult form", "shortest_name_length": 30}
{"curie": "MONDO:0005965", "names": ["Spinal stenosis", "Spinal stenoses", "SPINAL STENOSIS", "spinal stenosis", "Spinal Stenosis", "Stenosis;spinal", "Spinal Stenoses", "Stenosis, Spinal", "Stenoses, Spinal", "spinal; stenosis", "stenosis; spinal", "spinal narrowing", "Spinal stenosis NOS", "SS - Spinal stenosis", "Spinal stenosis, NOS", "lumbar spinal stenosis", "cervical spine stenosis", "Cervical spine stenosis", "Stenosis;spinal;cervical", "spinal stenosis cervical", "Spinal stenosis cervical", "cervical spinal stenosis", "CERVICAL SPINAL STENOSIS", "Cervical spinal stenosis", "Spinal stenosis (disorder)", "spinal stenosis (diagnosis)", "spinal stenosis of lumbar region", "Spinal stenosis, cervical region", "Spinal stenosis of lumbar region", "Spinal stenosis, site unspecified", "Spinal stenosis in cervical region", "cervical spine stenosis (diagnosis)", "Spinal stenosis, unspecified region", "Spinal stenosis in cervical region (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal stenosis", "shortest_name_length": 15}
{"curie": "UMLS:C4744565", "names": ["Metastatic Colon Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Colon Carcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0054741", "names": ["COXPD34", "Syndromic sensorineural deafness due to COXPD", "syndromic sensorineural deafness due to COXPD", "combined oxidative phosphorylation deficiency 34", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 34", "syndromic sensorineural hearing loss due to COXPD", "Syndromic sensorineural hearing loss due to COXPD", "syndromic sensorineural deafness due to combined oxidative phosphorylation defect", "Syndromic sensorineural deafness due to combined oxidative phosphorylation defect", "Syndromic sensorineural deafness due to COXPD (combined oxidative phosphorylation defect)", "Syndromic sensorineural deafness due to combined oxidative phosphorylation defect (disorder)", "Syndromic sensorineural hearing loss due to COXPD (combined oxidative phosphorylation defect)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation deficiency 34", "shortest_name_length": 7}
{"curie": "MONDO:0001411", "names": ["synostose", "SYNOSTOSIS", "synostoses", "synostosis", "Synostosis", "Synostoses", "Congenital abnormal Synostosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "synostosis", "shortest_name_length": 9}
{"curie": "MONDO:0018477", "names": ["KERNICTERUS", "Kernicterus", "kernicterus", "NUCLEAR JAUNDICE", "Jaundice nuclear", "Nuclear jaundice", "kernicterus; newborn", "kernicterus; jaundice", "jaundice; kernicterus", "kernicterus of newborn", "Kernicterus of newborn", "kernicterus (diagnosis)", "Kernicterus, unspecified", "bilirubin encephalopathy", "Bilirubin encephalopathy", "Bilirubin Encephalopathy", "Encephalopathy, Bilirubin", "Bilirubin Encephalopathies", "Kernicterus of newborn NOS", "Encephalopathies, Bilirubin", "Kernicterus of newborn, NOS", "kernicterus spectrum disorder", "Hyperbilirubinemic Encephalopathy", "Kernicterus of newborn (disorder)", "hyperbilirubinemic encephalopathy", "Encephalopathy, Hyperbilirubinemic", "encephalopathy; hyperbilirubinemic", "hyperbilirubinemic; encephalopathy", "kernicterus of newborn (diagnosis)", "Hyperbilirubinemic Encephalopathies", "Encephalopathies, Hyperbilirubinemic", "Kernicterus (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bilirubin encephalopathy", "shortest_name_length": 11}
{"curie": "UMLS:C0677951", "names": ["Stage I Hodgkin Lymphoma", "Stage I Hodgkin's Disease", "Hodgkin's Disease Stage I", "Hodgkin's disease stage I", "Hodgkin's Lymphoma Stage I", "Stage I Hodgkin's Lymphoma", "Hodgkin's disease NOS stage I", "Ann Arbor Stage I Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Hodgkin Lymphoma", "shortest_name_length": 24}
{"curie": "UMLS:C1377717", "names": ["Myeloid Leukemia in Remission", "Childhood Myeloid Leukemia in Remission", "myeloid leukemia in remission, childhood", "Childhood Nonlymphocytic Leukemia in Remission"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Myeloid Leukemia in Remission", "shortest_name_length": 29}
{"curie": "MONDO:0018211", "names": ["Balint syndrome", "Balint's syndrome", "Balint-Holmes syndrome", "Balint Holmes syndrome", "Balint syndrome (disorder)", "Balint syndrome (diagnosis)", "psychic paralysis of visual fixation", "Cortical paralysis of fixation syndrome", "Optic ataxia-gaze apraxia-simultanagnosia syndrome", "optic ataxia-gaze apraxia-simultanagnosia syndrome", "Optic ataxia, gaze apraxia, simultanagnosia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Balint syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0021535", "names": ["pancreas NET G1", "pancreatic NET G1", "Pancreatic NET G1", "pancreas carcinoid tumor", "Serotonin-producing PNET", "carcinoid tumor pancreas", "Carcinoid tumor of pancreas", "Carcinoid tumour of pancreas", "Carcinoid tumor of the pancreas", "carcinoid tumor of the pancreas", "Carcinoid tumour of the pancreas", "Pancreatic Neuroendocrine Tumor G1", "Serotonin-producing pancreatic NET", "pancreatic neuroendocrine tumor G1", "pancreas neuroendocrine neoplasm G1", "Pancreatic Serotonin Producing Tumor", "Serotonin-Producing Tumor of Pancreas", "Carcinoid tumor of pancreas (disorder)", "Pancreatic Serotonin Producing Neoplasm", "Serotonin-Producing Tumor of the Pancreas", "EC Cell, Serotonin Producing Pancreatic NET", "grade 1 neuroendocrine neoplasm of pancreas", "Serotonin-Producing Pancreatic Neuroendocrine Tumor", "Pancreatic Serotonin-Producing Neuroendocrine Tumor", "Serotonin-producing pancreatic neuroendocrine tumor", "Serotonin-producing neuroendocrine tumor of pancreas", "EC Cell, Serotonin Producing Pancreatic Neuroendocrine Tumor", "pancreas neuroendocrine tumor, well differentiated, low grade", "Serotonin-Producing Tumors With and Without Carcinoid Syndrome", "Enterochromaffin Cell Serotonin-Producing Pancreatic Neuroendocrine Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic neuroendocrine tumor G1", "shortest_name_length": 15}
{"curie": "MONDO:0054731", "names": ["SPGF27", "spermatogenic failure 27", "SPERMATOGENIC FAILURE 27"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 27", "shortest_name_length": 6}
{"curie": "UMLS:C0158951", "names": ["Fetal bleeding", "Foetal bleeding", "Fetal blood loss", "fetal hemorrhage", "Fetal hemorrhage", "Hemorrhage fetal", "Fetal Blood Loss", "hemorrhage; fetal", "fetal; hemorrhage", "Fetal haemorrhage", "Foetal blood loss", "Haemorrhage foetal", "Foetal haemorrhage", "Hemorrhage NOS fetal", "Haemorrhage NOS foetal", "Fetal blood loss (disorder)", "fetal hemorrhage (diagnosis)", "Fetal blood loss, unspecified", "Fetal blood loss affecting newborn"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fetal blood loss", "shortest_name_length": 14}
{"curie": "MONDO:0013594", "names": ["SCA36", "Asidan", "Asidan ataxia", "Costa de Morte ataxia", "SPINOCEREBELLAR ATAXIA 36", "spinocerebellar ataxia 36", "Spinocerebellar ataxia 36", "Spinocerebellar Ataxia Type 36", "spinocerebellar ataxia type 36", "Spinocerebellar ataxia type 36", "Spinocerebellar ataxia type 36 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia type 36", "shortest_name_length": 5}
{"curie": "MONDO:0004805", "names": ["wbc disease", "WBC diseases", "leukocyte disease", "leukocyte disorder", "Leukocyte Disorder", "Leukocyte Disorders", "Leucocyte disorders", "leukocyte disorders", "Disorder, Leukocyte", "disorder, leukocyte", "disorders, leukocyte", "disease of leukocyte", "Disorders, Leukocyte", "disorder of leukocyte", "white blood cell disease", "disease white blood cell", "white blood cell disorder", "blood cell diseases white", "White blood cell disorder", "white blood cell disorders", "White blood cell disorders", "WHITE BLOOD CELL DISORDERS", "Diseases of white blood cells", "diseases of white blood cells", "White blood cell disorder NOS", "leukocyte disease or disorder", "White blood cell disorder, NOS", "disease or disorder of leukocyte", "White blood cell disorder (disorder)", "white blood cell disorders (diagnosis)", "Unspecified disease of white blood cells", "disease (or disorder); white blood cells", "Disease of white blood cells, unspecified", "WHITE BLOOD CELL DISORDERS: GENERAL TERMS", "Disorder of white blood cells, unspecified", "White blood cell disorder, disease or syndrome", "White Blood Cell Disorders, Diseases and Syndromes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukocyte disorder", "shortest_name_length": 11}
{"curie": "MONDO:0024454", "names": ["Sacral plexopathy", "sacral plexopathy", "sacral nerve plexus disorder", "disease of sacral nerve plexus", "disorder of sacral nerve plexus", "sacral nerve plexus disease or disorder", "disease or disorder of sacral nerve plexus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sacral nerve plexus disorder", "shortest_name_length": 17}
{"curie": "MONDO:0011578", "names": ["Prn1", "PRN1", "PTCPRN", "Ptcprn", "ptc-RCC", "Papillary thyroid carcinoma with renal papillary neoplasia", "thyroid carcinoma, papillary, with papillary renal neoplasia", "THYROID CARCINOMA, PAPILLARY, WITH PAPILLARY RENAL NEOPLASIA", "Thyroid Carcinoma, Papillary, With Papillary Renal Neoplasia", "familial papillary thyroid carcinoma with renal papillary neoplasia", "Papillary thyroid carcinoma with renal papillary neoplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial papillary thyroid carcinoma with renal papillary neoplasia", "shortest_name_length": 4}
{"curie": "MONDO:0010634", "names": ["jaundice, familial obstructive, of infancy", "JAUNDICE, FAMILIAL OBSTRUCTIVE, OF INFANCY", "Jaundice, Familial Obstructive, of Infancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "jaundice, familial obstructive, of infancy", "shortest_name_length": 42}
{"curie": "MONDO:0030337", "names": ["ARCL2E", "cutis laxa, autosomal recessive, type 2E", "CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIE", "cutis laxa, autosomal recessive, type IIE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutis laxa, autosomal recessive, type 2E", "shortest_name_length": 6}
{"curie": "MONDO:0007863", "names": ["Kleine-Levin", "Periodic Hypersomnia", "Kleine-Levin syndrome", "Kleine-Levin Syndrome", "kleine-levin syndrome", "Hypersomnia, Periodic", "Kleine Levin Syndrome", "Kleine Levin syndrome", "Periodic Hypersomnias", "kleine levin syndrome", "KLEINE-LEVIN SYNDROME", "Syndrome, Kleine-Levin", "Hypersomnia-bulimia syndrome", "syndrome; hypersomnia-bulimia", "familial hibernation syndrome", "hypersomnia-bulimia; syndrome", "familial Kleine-Levin syndrome", "Kleine-Levin-Critchley Syndrome", "Kleine Levin Critchley Syndrome", "Kleine-Levin syndrome (disorder)", "Syndrome, Kleine-Levin-Critchley", "Kleine Levin Hibernation Syndrome", "Kleine Levin syndrome (diagnosis)", "Kleine-LEVIN hibernation syndrome", "KLEINE-LEVIN HIBERNATION SYNDROME", "Kleine-Levin Hibernation Syndrome", "Hibernation Syndrome, Kleine-Levin", "Syndrome, Kleine-Levin Hibernation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kleine-Levin syndrome", "shortest_name_length": 12}
{"curie": "UMLS:C0861572", "names": ["Mouth Verrucous Carcinoma in situ", "Stage 0 Mouth Verrucous Carcinoma", "Stage 0 Verrucous Carcinoma of Mouth", "Verrucous Carcinoma in situ of Mouth", "Oral Cavity Verrucous Carcinoma in situ", "Stage 0 Oral Cavity Verrucous Carcinoma", "Verrucous Carcinoma in situ of the Mouth", "Stage 0 Verrucous Carcinoma of the Mouth", "Verrucous Carcinoma in situ of Oral Cavity", "Stage 0 Verrucous Carcinoma of Oral Cavity", "Stage 0 Verrucous Carcinoma of the Oral Cavity", "Verrucous carcinoma of the oral cavity stage 0", "Verrucous Carcinoma in situ of the Oral Cavity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Verrucous carcinoma of the oral cavity stage 0", "shortest_name_length": 33}
{"curie": "UMLS:C4527179", "names": ["Stage IB", "Stage IB Cutaneous (Skin) Melanoma", "Pathologic Stage IB Cutaneous Melanoma AJCC v8", "Pathologic Stage IB Melanoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IB Cutaneous Melanoma AJCC v8", "shortest_name_length": 8}
{"curie": "MONDO:0017402", "names": ["familial isolated arrhythmogenic ventricular dysplasia, biventricular form", "familial isolated arrhythmogenic ventricular cardiomyopathy, biventricular form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial isolated arrhythmogenic ventricular dysplasia, biventricular form", "shortest_name_length": 74}
{"curie": "MONDO:0015447", "names": ["differentiated thyroid cancer", "Differentiated Thyroid Cancer", "Differentiated thyroid cancer", "Differentiated Thyroid Carcinoma", "differentiated thyroid carcinoma", "Differentiated thyroid carcinoma", "Well-Differentiated Thyroid Cancer", "well-differentiated thyroid cancer", "Differentiated Thyroid Gland Cancer", "DTC - differentiated thyroid cancer", "differentiated thyroid gland cancer", "well-differentiated thyroid carcinoma", "well differentiated thyroid carcinoma", "Well Differentiated Thyroid Carcinoma", "Well-differentiated thyroid carcinoma", "differentiated thyroid gland carcinoma", "Thyroid Gland Differentiated Carcinoma", "Differentiated Thyroid Gland Carcinoma", "thyroid gland differentiated carcinoma", "papillary or follicular thyroid carcinoma", "Papillary or follicular thyroid carcinoma", "Well Differentiated Thyroid Gland Carcinoma", "well differentiated thyroid gland carcinoma", "thyroid gland well differentiated carcinoma", "Differentiated thyroid carcinoma (disorder)", "Thyroid Gland Well Differentiated Carcinoma", "Follicular/Papillary Thyroid Gland Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "differentiated thyroid carcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0006207", "names": ["fallopian tube carcinosarcoma", "Fallopian Tube Carcinosarcoma", "carcinosarcoma of fallopian tube", "carcinosarcoma of fallopian tube (diagnosis)", "fallopian tube malignant mixed Mullerian tumor", "Fallopian Tube Malignant Mixed Mesodermal (Müllerian) Tumor", "fallopian tube malignant mixed mesodermal (Müllerian) tumor", "fallopian tube malignant mixed mesodermal (mullerian) tumor", "Fallopian Tube Malignant Mixed Mesodermal (Mullerian) Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fallopian tube carcinosarcoma", "shortest_name_length": 29}
{"curie": "MONDO:0011483", "names": ["PCBD", "Pcbd", "polycystic bone disease", "POLYCYSTIC BONE DISEASE", "Polycystic bone disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polycystic bone disease", "shortest_name_length": 4}
{"curie": "UMLS:C1266157", "names": ["GCNIS", "IGCNU", "Gonocytoma In Situ", "Intratubular germ cell neoplasia", "Intratubular malignant germ cells", "Testicular Intraepithelial Neoplasia", "Testicular Germ Cell Neoplasia In Situ", "Testicular Intratubular Germ Cell Neoplasia", "Testicular Intratubular Germ Cell Neoplasia, Unclassified", "Intratubular malignant germ cells (morphologic abnormality)", "Testicular Intratubular Germ Cell Neoplasia of Unclassified Type", "Testicular Intratubular Germ Cell Neoplasia of the Unclassified Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intratubular malignant germ cells", "shortest_name_length": 5}
{"curie": "MONDO:0007848", "names": ["Hereditary keratitis", "hereditary keratitis", "Keratitis, hereditary", "keratitis, hereditary", "KERATITIS, HEREDITARY", "autosomal dominant keratitis", "Autosomal dominant keratitis", "keratitis, autosomal dominant", "KERATITIS, AUTOSOMAL DOMINANT", "Dominantly inherited keratitis", "dominantly inherited keratitis", "Autosomal dominant keratitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant keratitis", "shortest_name_length": 20}
{"curie": "MONDO:0019697", "names": ["mesomelic and rhizo-mesomelic dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mesomelic and rhizo-mesomelic dysplasia", "shortest_name_length": 39}
{"curie": "UMLS:C0677947", "names": ["Colorectal cancer Dukes A", "Colorectal cancer stage I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal cancer stage I", "shortest_name_length": 25}
{"curie": "UMLS:C5556897", "names": ["Male Reproductive System Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Male Reproductive System Carcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0014558", "names": ["MRD32", "ARTHS", "KAT6A SYNDROME", "KAT6A Syndrome", "MRD32, FORMERLY", "Arboleda Tham syndrome", "ARBOLEDA-THAM SYNDROME", "Arboleda-Tham syndrome", "autosomal dominant mental retardation 32", "mental retardation, autosomal dominant 32", "autosomal dominant intellectual disability 32", "mental retardation, autosomal dominant type 32", "intellectual disability, autosomal dominant 32", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 32, FORMERLY", "intellectual disability, autosomal dominant type 32", "autosomal dominant non-syndromic intellectual disability 32", "autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome", "Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome", "Autosomal dominant intellectual disability, craniofacial anomalies, cardiac defects syndrome", "Autosomal dominant intellectual disability, craniofacial anomalies, cardiac defects syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C1699140", "names": ["Large Intestinal Mucositis", "Large intestinal mucositis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Large intestinal mucositis", "shortest_name_length": 26}
{"curie": "UMLS:C1518700", "names": ["Ovarian Dermoid Cyst with Melanocytic Nevus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Dermoid Cyst with Melanocytic Nevus", "shortest_name_length": 43}
{"curie": "MONDO:0020194", "names": ["congenital alacrima"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital alacrima", "shortest_name_length": 19}
{"curie": "UMLS:C0854988", "names": ["Stage IV Lung Adenocarcinoma", "Lung adenocarcinoma stage IV", "Adenocarcinoma lung stage IV", "Lung Adenocarcinoma, Stage IV", "Lung adenocarcinoma metastatic", "Stage IV Adenocarcinoma of Lung", "Adenocarcinoma of lung stage IV", "Adenocarcinoma of lung, stage IV", "Stage IV Adenocarcinoma of the Lung", "Stage IV Lung Adenocarcinoma AJCC v7", "Adenocarcinoma of lung, stage IV (disorder)", "Finding of adenocarcinoma of lung, stage IV", "clinical finding tumor stage adenocarcinoma of lung, stage IV", "Finding of adenocarcinoma of lung, stage IV (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma of lung, stage IV", "shortest_name_length": 28}
{"curie": "UMLS:C1520133", "names": ["Well Differentiated Ovarian Steroid Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Well Differentiated Ovarian Steroid Cell Tumor", "shortest_name_length": 46}
{"curie": "MONDO:0006132", "names": ["Cervical Adenoid Basal Cancer", "cervical adenoid basal cancer", "cervical adenoid basal carcinoma", "Cervical Adenoid Basal Carcinoma", "Cervical adenoid basal carcinoma", "Adenoid basal carcinoma of cervix uteri", "Adenoid basal carcinoma of the cervix uteri", "Adenoid basal carcinoma of cervix uteri (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical adenoid basal carcinoma", "shortest_name_length": 29}
{"curie": "UMLS:C0456107", "names": ["Neonatal meningitis", "Meningitis neonatal", "meningitis neonatal", "neonatal meningitis", "Neonatal meningitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neonatal meningitis", "shortest_name_length": 19}
{"curie": "MONDO:0011609", "names": ["ATOD6", "atopic dermatitis 6", "DERMATITIS, ATOPIC, 6", "dermatitis, ATOPIC, 6", "dermatitis, atopic, 6", "Dermatitis, Atopic, 6", "atopic dermatitis type 6", "dermatitis, atopic, susceptibility to, 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermatitis, atopic, 6", "shortest_name_length": 5}
{"curie": "MONDO:0019078", "names": ["3C SYNDROME", "3C syndrome", "CCC dysplasia", "Ritscher Schinzel syndrome", "Ritscher-Schinzel Syndrome", "Ritscher-Schinzel syndrome", "Dandy-Walker-like syndrome", "Craniocerebellocardiac dysplasia", "CRANIOCEREBELLOCARDIAC DYSPLASIA", "craniocerebellocardiac dysplasia", "cranio-cerebello-cardiac dysplasia", "Dandy-Walker-like malformation with ASD", "Cranio-cerebello-cardiac dysplasia syndrome", "Ritscher-Schinzel cranio-cerebello-cardiac syndrome", "Cranio-cerebello-cardiac dysplasia syndrome (disorder)", "cranio-cerebello-cardiac (3C, CCC) dysplasia or syndrome", "DANDY-WALKER-LIKE MALFORMATION WITH ATRIOVENTRICULAR SEPTAL DEFECT", "Dandy-Walker-like malformation with atrioventricular septal defect", "Dandy-Walker like malformation with atrioventricular septal defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ritscher-Schinzel syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0030721", "names": ["SPGF68", "SPERMATOGENIC FAILURE 68", "spermatogenic failure 68"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 68", "shortest_name_length": 6}
{"curie": "MONDO:0032776", "names": ["DFNB99", "autosomal recessive deafness 99", "DEAFNESS, AUTOSOMAL RECESSIVE 99", "deafness, autosomal recessive 99", "hearing loss, autosomal recessive 99", "autosomal recessive nonsyndromic deafness 99"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal recessive 99", "shortest_name_length": 6}
{"curie": "UMLS:C4525118", "names": ["Stage I Colon Cancer", "Stage I Colon Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Colon Cancer AJCC v8", "shortest_name_length": 20}
{"curie": "MONDO:0020979", "names": ["Pilosebaceous Hamartoma", "pilosebaceous hamartoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pilosebaceous hamartoma", "shortest_name_length": 23}
{"curie": "UMLS:C0030445", "names": ["Obstetric Paralyses", "obstetric paralysis", "Obstetric Paralysis", "Paralyses, Obstetric", "Paralysis, Obstetric", "Obstetrical Paralysis", "Obstetrical paralysis", "Obstetrical Paralyses", "obstetrical paralysis", "Paralysis, Obstetrical", "Paralyses, Obstetrical"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paralysis, Obstetric", "shortest_name_length": 19}
{"curie": "MONDO:0006715", "names": ["coronary stenosis", "stenosis coronary", "Coronary Stenoses", "Coronary Stenosis", "stenosis; coronary", "coronary; stenosis", "Stenoses, Coronary", "Stenosis, Coronary", "a.coronaria; narrowing", "Coronary Artery Stenosis", "Narrow coronary arteries", "artery coronary stenosis", "coronary artery stenosis", "Coronary artery stenosis", "Coronary Artery Stenoses", "Stenoses, Coronary Artery", "Artery Stenosis, Coronary", "Stenosis, Coronary Artery", "Artery Stenoses, Coronary", "artery; stenosis, coronary", "stenosis; artery, coronary", "narrowing; coronary artery", "Coronary arteries--Stenosis", "Narrowing of coronary artery", "Coronary artery stenosis (disorder)", "coronary artery stenosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coronary stenosis", "shortest_name_length": 17}
{"curie": "MONDO:0018017", "names": ["GCC", "Goblet cell tumor", "goblet cell tumor", "mucinous carcinoid", "Mucinous carcinoid", "Mucocarcinoid tumor", "Mucocarcinoid tumour", "Goblet Cell Carcinoid", "Goblet cell carcinoma", "goblet cell carcinoma", "Goblet cell carcinoid", "goblet cell carcinoid", "goblet cell; carcinoid", "Goblet Cell Carcinoids", "carcinoid; goblet cell", "Carcinoid, Goblet Cell", "Carcinoids, Goblet Cell", "Mucinous Carcinoid Tumor", "carcinoma of goblet cell", "mucinous carcinoid tumor", "goblet cell adenocarcinoid", "Goblet cell adenocarcinoid", "goblet cell carcinoid tumor", "Goblet Cell Carcinoid Tumor", "Appendix Adenocarcinoid Tumor", "appendix adenocarcinoid tumor", "Mucocarcinoid tumor, malignant", "Appendix Goblet Cell Carcinoid", "appendix goblet cell carcinoid", "Mucocarcinoid tumour, malignant", "adenocarcinoid tumor of appendix", "[M]Mucocarcinoid tumor, malignant", "goblet cell carcinoid of appendix", "goblet cell carcinoid (diagnosis)", "[M]Mucocarcinoid tumour, malignant", "Appendix Goblet Cell Adenocarcinoma", "Appendix Goblet Cell Carcinoid Tumor", "appendix goblet cell carcinoid tumor", "Adenocarcinoid tumor of the appendix", "goblet cell carcinoid of the appendix", "Adenocarcinoid tumour of the appendix", "tumor; mucocarcinoid, unspecified site", "mucocarcinoid; tumor, unspecified site", "Appendix Mixed Carcinoid-Adenocarcinoma", "appendix mixed carcinoid-adenocarcinoma", "adenocarcinoid tumor of appendix (diagnosis)", "goblet cell carcinoid of appendix (diagnosis)", "Goblet cell carcinoid (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "goblet cell carcinoma", "shortest_name_length": 3}
{"curie": "MONDO:0100451", "names": ["MKS4", "SLSN6", "LCA10", "JBTS5", "BBS14", "Meckel syndrome 4", "CEP290 ciliopathy", "Joubert syndrome 5", "CEP290 Meckel syndrome", "Meckel syndrome, type 4", "Joubert syndrome type 5", "CEP290 Joubert syndrome", "SENIOR-Loken syndrome 6", "Senior-Loken syndrome 6", "Bardet-Biedl syndrome 14", "CEP290-related ciliopathy", "CEP290 Senior-Loken syndrome", "Senior-Loken syndrome type 6", "Leber congenital amaurosis 10", "Bardet-Biedl syndrome type 14", "Meckel-Gruber syndrome, type 4", "CEP290 Leber congenital amaurosis", "Leber congenital amaurosis type 10", "amaurosis congenita of Leber, type 10", "Meckel-like Cerebrorenodigital syndrome", "Meckel syndrome caused by mutation in CEP290", "Joubert syndrome caused by mutation in CEP290", "Senior-Loken syndrome caused by mutation in CEP290", "Leber congenital amaurosis caused by mutation in CEP290"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CEP290-related ciliopathy", "shortest_name_length": 4}
{"curie": "UMLS:C4525692", "names": ["Appendix Neuroendocrine Tumor by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Appendix Neuroendocrine Tumor by AJCC v8 Stage", "shortest_name_length": 46}
{"curie": "MONDO:0007485", "names": ["DKCA", "DKCA1", "dyskeratosis congenita Scoggins type", "dyskeratosis congenita, Scoggins type", "Dyskeratosis Congenita, Scoggins Type", "DYSKERATOSIS CONGENITA, SCOGGINS TYPE", "dyskeratosis congenita autosomal dominant", "autosomal dominant dyskeratosis congenita", "Autosomal dominant dyskeratosis congenita", "DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT", "Dyskeratosis Congenita, Autosomal Dominant", "autosomal dominant dyskeratosis congenita 1", "DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 1", "dyskeratosis congenita, autosomal dominant 1", "Dyskeratosis Congenita, Autosomal Dominant 1", "dyskeratosis congenita, autosomal dominant type 1", "Autosomal dominant dyskeratosis congenita (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyskeratosis congenita, autosomal dominant 1", "shortest_name_length": 4}
{"curie": "UMLS:C0340654", "names": ["Arterial bleed", "Arterial bleeding", "artery; hemorrhage", "Arterial hemorrhage", "Arterial haemorrhage", "hemorrhage; arterial", "Arterial hemorrhage NOS", "Arterial haemorrhage NOS", "Arterial hemorrhage (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arterial hemorrhage", "shortest_name_length": 14}
{"curie": "MONDO:0054593", "names": ["MCPH18", "primary autosomal dominant microcephaly 18", "microcephaly 18, primary, autosomal dominant", "MICROCEPHALY 18, PRIMARY, AUTOSOMAL DOMINANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly 18, primary, autosomal dominant", "shortest_name_length": 6}
{"curie": "UMLS:C2983705", "names": ["Colorectal Cancer by AJCC v6 Stage", "Colorectal Carcinoma by AJCC v6 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Cancer by AJCC v6 Stage", "shortest_name_length": 34}
{"curie": "MONDO:0019556", "names": ["Semicircular lipoatrophy", "semicircular lipoatrophy", "Lipoatrophia semicircularis", "lipoatrophia semicircularis", "Semicircular lipoatrophy (disorder)", "Pressure-induced localized lipoatrophy", "pressure-induced localized lipoatrophy", "Linear circular atrophy of lower extremities", "Linear circular atrophy of lower extremities (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pressure-induced localized lipoatrophy", "shortest_name_length": 24}
{"curie": "MONDO:0021469", "names": ["Benign Anal Tumor", "benign anal tumor", "benign anal neoplasm", "benign tumor of anus", "Benign Anal Neoplasm", "Benign Tumor of Anus", "Benign tumor of anus", "anus benign neoplasm", "Benign tumour of anus", "benign neoplasm of anus", "Benign Neoplasm of Anus", "Benign neoplasm of anus", "benign tumor of the anus", "Benign Tumor of the Anus", "Benign neoplasm of anus NOS", "benign neoplasm of the anus", "Benign Neoplasm of the Anus", "Benign neoplasm of anus (disorder)", "benign neoplasm of anus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of anus", "shortest_name_length": 17}
{"curie": "MONDO:0016689", "names": ["Gemistocytoma", "Gemistocytic astrocytoma", "Gemistocytic Astrocytoma", "gemistocytic astrocytoma", "Astrocytoma, Gemistocytic", "Gemistocytic Astrocytomas", "gemistocytic astrocytic tumor", "Gemistocytic Astrocytic tumor", "gemistocytic astrocytoma (morphologic abnormality)", "Gemistocytic astrocytoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gemistocytic astrocytoma", "shortest_name_length": 13}
{"curie": "MONDO:0020365", "names": ["CHED1", "CHEDI", "Autosomal dominant CHED", "autosomal dominant CHED", "congenital hereditary endothelial dystrophy type 1", "congenital hereditary endothelial dystrophy type I", "Congenital hereditary endothelial dystrophy type 1", "Congenital hereditary endothelial dystrophy type I", "congenital hereditary endothelial dystrophy, CHED 1", "CHED1 - congenital hereditary endothelial dystrophy type 1", "Congenital hereditary endothelial dystrophy type 1 (disorder)", "autosomal dominant congenital hereditary endothelial dystrophy", "Autosomal dominant congenital hereditary endothelial dystrophy", "congenital hereditary endothelial dystrophy, CHED 1 (diagnosis)", "Congenital hereditary endothelial dystrophy autosomal dominant form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital hereditary endothelial dystrophy type I", "shortest_name_length": 5}
{"curie": "UMLS:C5237826", "names": ["Advanced Colorectal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Colorectal Adenocarcinoma", "shortest_name_length": 34}
{"curie": "UMLS:C4289589", "names": ["Endometrial Dedifferentiated Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endometrial Dedifferentiated Carcinoma", "shortest_name_length": 38}
{"curie": "MONDO:0014540", "names": ["AI1H", "ITGB6 amelogenesis imperfecta", "amelogenesis imperfecta type 1H", "amelogenesis imperfecta type IH", "AMELOGENESIS IMPERFECTA, TYPE IH", "amelogenesis imperfecta, type IH", "amelogenesis imperfecta, type 1H", "amelogenesis imperfecta caused by mutation in ITGB6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amelogenesis imperfecta type 1H", "shortest_name_length": 4}
{"curie": "UMLS:C0026771", "names": ["Polytrauma", "Polytraumas", "Multiple Wound", "Polytraumatism", "Multiple Trauma", "trauma multiple", "Multiple trauma", "Trauma;multiple", "Multiple Injury", "TRAUMA MULTIPLE", "Injury;multiple", "Multiple wounds", "multiple trauma", "multiple; wound", "multiple wounds", "Wound, Multiple", "Multiple Wounds", "wound; multiple", "Multiple Traumas", "Wounds, Multiple", "Trauma, Multiple", "Injury, Multiple", "multiple injuries", "Multiple Injuries", "multiples traumas", "Traumas, Multiple", "Multiple injuries", "Injuries, Multiple", "Multiple injuries, NOS", "Multiple traumatic injuries", "Multiple injuries (disorder)", "Multiple injuries - disorder", "multiple injuries (diagnosis)", "Unspecified multiple injuries", "multiple wounds (physical finding)", "Multiple traumatic injuries (disorder)", "Multiple wounds (morphologic abnormality)", "Multiple injuries (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Multiple Trauma", "shortest_name_length": 10}
{"curie": "MONDO:0012213", "names": ["SPG26", "spastic paraplegia 26", "GM2 synthase deficiency", "hereditary spastic paraplegia 26", "hereditary spastic paraplegia type 26", "autosomal recessive spastic paraplegia 26", "SPASTIC PARAPLEGIA 26, AUTOSOMAL RECESSIVE", "spastic paraplegia 26, autosomal recessive", "Spastic paraplegia 26, autosomal recessive", "Autosomal recessive spastic paraplegia type 26", "autosomal recessive spastic paraplegia type 26", "SPASTIC PARAPLEGIA 26, AUTOSOMAL RECESSIVE (disorder)", "familial spastic paraplegia autosomal recessive type 26", "Autosomal recessive spastic paraplegia type 26 (disorder)", "Autosomal recessive spastic paraplegia type 26 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 26", "shortest_name_length": 5}
{"curie": "MONDO:0016758", "names": ["Franek-Bocker-Kahlen syndrome", "microcephaly brain defect spasticity hypernatremia", "microcephaly - brain defect - spasticity - hypernatremia", "microcephaly-brain defect-spasticity-hypernatremia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly-brain defect-spasticity-hypernatremia syndrome", "shortest_name_length": 29}
{"curie": "MONDO:0010895", "names": ["ABCDS", "ABCD syndrome", "ABCD SYNDROME", "Albinism, Black lock, Cell migration disorder of the neurocytes of the gut, and Deafness", "albinism, black lock, cell migration disorder of the neurocytes of the gut, and deafness", "ALBINISM, BLACK LOCK, CELL MIGRATION DISORDER OF THE NEUROCYTES OF THE GUT, AND DEAFNESS", "albinism, black lock, cell migration disorder of the Neurocytes of the gut, and deafness", "albinism, block lock, cell migration disorder of the neurocytes of the gut, and deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ABCD syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0700438", "names": ["sick headache", "Sick headache", "Sick Headache", "SICK HEADACHE", "Sick headaches", "Sick Headaches", "Headache, Sick", "Headaches, Sick", "Sick headache (disorder)", "Sick headache (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sick Headaches", "shortest_name_length": 13}
{"curie": "MONDO:0002365", "names": ["Renal Hemangiopericytoma", "renal hemangiopericytoma", "kidney hemangiopericytoma", "Kidney Hemangiopericytoma", "kidney spindle cell tumor", "Hemangiopericytoma of kidney", "hemangiopericytoma of kidney", "Hemangiopericytoma of Kidney", "Haemangiopericytoma of kidney", "hemangiopericytoma of the kidney", "Hemangiopericytoma of the Kidney", "Hemangiopericytoma of kidney (disorder)", "Hemangiopericytoma of kidney (diagnosis)", "renal neoplasm benign hemangiopericytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kidney hemangiopericytoma", "shortest_name_length": 24}
{"curie": "UMLS:C5552974", "names": ["AMDP", "Acromesomelic Dysplasia, PRKG2 Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acromesomelic Dysplasia, PRKG2 Type", "shortest_name_length": 4}
{"curie": "MONDO:0010411", "names": ["IHPS4", "PYLORIC STENOSIS, INFANTILE HYPERTROPHIC, 4", "pyloric stenosis, infantile hypertrophic, 4", "Pyloric Stenosis, Infantile Hypertrophic, 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyloric stenosis, infantile hypertrophic, 4", "shortest_name_length": 5}
{"curie": "MONDO:0016659", "names": ["Trisomy 8p23.1", "trisomy 8p23.1", "dup(8)(p23.1p23.1)", "Dup(8)(p23.1p23.1)", "8p23.1 duplication syndrome", "8q21.11 Microdeletion Syndrome", "8p23.1 duplication syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "8p23.1 duplication syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0008195", "names": ["PMC", "Eulenburg", "Eulenburg disease", "Eulenburg Disease", "EULENBURG DISEASE", "Eulenburg syndrome", "eulenburg's disease", "Eulenburg's Disease", "Eulenburg's disease", "Von Eulenberg Disease", "Paramyotonia Congenita", "PARAMYOTONIA CONGENITA", "Paramyotonia congenita", "paramyotonia congenita", "congenital paramyotonia", "Von Eulenberg's disease", "Von Eulenberg's Disease", "myotonia congenita intermittens", "Paralysis Periodica Paramyotonia", "Paramyotonia congenita (disorder)", "PARALYSIS PERIODICA PARAMYOTONICA", "paralysis periodica paramyotonica", "paralysis periodica Paramyotonica", "Paramyotonia Congenita (disorder)", "congenital paramyotonia (diagnosis)", "Von Eulenburg paramyotonia congenita", "paramyotonia congenita of VON Eulenburg", "Paramyotonia Congenita of von Eulenburg", "PARAMYOTONIA CONGENITA OF VON EULENBURG", "Paramyotonia congenita of Von Eulenburg", "paramyotonia congenita of Von Eulenburg", "Paramyotonia Congenita of von Eulenberg", "Paramyotonia congenita (of von Eulenburg)", "Paramyotonia Congenita without Cold Paralysis", "paramyotonia congenita without cold paralysis", "Paramyotonia Congenita Without Cold Paralysis", "PARAMYOTONIA CONGENITA WITHOUT COLD PARALYSIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paramyotonia congenita of Von Eulenburg", "shortest_name_length": 3}
{"curie": "UMLS:C1336359", "names": ["Stage IVA Pharyngeal Cancer", "Stage IVA Pharynx Carcinoma", "Pharyngeal Cancer Stage IVA", "Stage IVA Pharyngeal Carcinoma", "Stage IVA Carcinoma of Pharynx", "Stage IVA Carcinoma of the Pharynx"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Pharyngeal Carcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0012876", "names": ["THPH10", "HCF2 DEFICIENCY", "Hcf2 deficiency", "Hcf 2 deficiency", "HCF 2 deficiency", "Hcf II Deficiency", "HCF II DEFICIENCY", "HCF II deficiency", "heparin cofactor 2 deficiency", "HEPARIN COFACTOR II DEFICIENCY", "Heparin cofactor II deficiency", "Heparin Cofactor II Deficiency", "heparin cofactor II deficiency", "Heparin cofactor II deficiency (disorder)", "thrombophilia due to heparin cofactor 2 deficiency", "thrombophilia due to heparin cofactor II deficiency", "THROMBOPHILIA DUE TO HEPARIN COFACTOR II DEFICIENCY", "thrombophilia 10 due to heparin cofactor II deficiency", "Thrombophilia, Susceptibility to, due to Heparin Cofactor Ii Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heparin cofactor 2 deficiency", "shortest_name_length": 6}
{"curie": "MONDO:0004630", "names": ["substance-induced psychosis", "Other specified transient organic mental disorders", "Other specified transient mental disorders due to conditions classified elsewhere, other"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "substance-induced psychosis", "shortest_name_length": 27}
{"curie": "MONDO:0001634", "names": ["Bladder leiomyoma", "Bladder Leiomyoma", "bladder leiomyoma", "Leiomyoma of Bladder", "leiomyoma of bladder", "leiomyoma of the bladder", "Leiomyoma of the Bladder", "Urinary Bladder Leiomyoma", "urinary bladder leiomyoma", "Leiomyoma of Urinary Bladder", "leiomyoma of urinary bladder", "leiomyoma of the urinary bladder", "Leiomyoma of the Urinary Bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder leiomyoma", "shortest_name_length": 17}
{"curie": "MONDO:0004806", "names": ["EOSINOPHILOSIS, PULMONARY", "Pneumonia eosinophilic chronic", "EOSINOPHILIC PNEUMONIA CHRONIC", "Chronic Eosinophilic Pneumonia", "Chronic pulmonary eosinophilia", "chronic eosinophilic pneumonia", "Eosinophilic pneumonia chronic", "CHRONIC EOSINOPHILIC PNEUMONIA", "Chronic eosinophilic pneumonia", "PNEUMONIA, CHRONIC EOSINOPHILIC", "eosinophilic pneumonia, chronic", "Prolonged pulmonary eosinophilia", "EOSINOPHILIA, PROLONGED PULMONARY", "Idiopathic pulmonary eosinophilia", "Cryptogenic eosinophilic pneumonia", "cryptogenic pulmonary eosinophilia", "Cryptogenic pulmonary eosinophilia", "chronic eosinophilic pneumonia (diagnosis)", "Cryptogenic pulmonary eosinophilia (disorder)", "PULMONARY INFILTRATION, PROLONGED EOSINOPHILIC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic eosinophilic pneumonia", "shortest_name_length": 25}
{"curie": "MONDO:0002884", "names": ["nail disease", "Nail disease", "disease nail", "Nail Disease", "NAIL DISEASE", "nail disorder", "NAIL DISORDER", "Nail disorder", "Abnormal Nail", "nail diseases", "DISORDER NAIL", "Nail Diseases", "disorder nail", "Disease, Nail", "diseases nail", "disease nails", "nails disease", "Disorder nail", "Nail Disorders", "Abnormal Nails", "Abnormal nails", "nails diseases", "Nail, Abnormal", "Diseases, Nail", "Nail disorders", "nail disorders", "nail; disorder", "disorders nail", "Malformed Nail", "diseases nails", "of nail disease", "Nails, Abnormal", "Malformed Nails", "Nail, Malformed", "Malformed nails", "disease of nail", "Disease;nail(s)", "Disorder of nail", "Nail abnormality", "Nails, Malformed", "Diseases of nail", "Nail Abnormality", "of nail diseases", "disorder of nail", "nail abnormality", "disease of nails", "Abnormality, Nail", "Nail disorder NOS", "abnormalities nail", "Nail abnormalities", "Nail Abnormalities", "Abnormalities, Nail", "abnormalities nails", "Disease of nail, NOS", "disease of the nails", "Nail abnormality NOS", "diseases of the nails", "DISEASES OF THE NAILS", "disease disorders nail", "Abnormality of the nail", "diseases disorders nail", "nail disease or disorder", "Nail disorder, unspecified", "disease or disorder of nail", "Unspecified disease of nail", "Disorder of nail (disorder)", "disease of nails (diagnosis)", "disease (or disorder); nails", "Disease of nail, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nail disorder", "shortest_name_length": 12}
{"curie": "UMLS:C4724395", "names": ["Metastatic Nasopharyngeal Squamous Cell Carcinoma", "Metastatic Nasopharyngeal Throat Squamous Cell Cancer", "Metastatic Squamous Cell Carcinoma of the Nasopharynx"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Squamous Cell Carcinoma of the Nasopharynx", "shortest_name_length": 49}
{"curie": "MONDO:0011817", "names": ["CHDS1", "Chds1", "CX3CR1 coronary artery disease", "coronary artery disease, resistance to", "coronary heart disease, susceptibility to", "coronary heart disease, susceptibility to, 1", "CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 1", "coronary heart disease, susceptibility to, type 1", "coronary artery disease caused by mutation in CX3CR1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coronary heart disease, susceptibility to, 1", "shortest_name_length": 5}
{"curie": "MONDO:0018580", "names": ["PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome", "shortest_name_length": 71}
{"curie": "UMLS:C1332577", "names": ["Bone Glomus Tumor", "Glomus Tumor of Bone", "Bone Glomus Neoplasm", "Osseous Glomus Tumor", "Glomus Neoplasm of Bone", "Osseous Glomus Neoplasm", "Glomus Tumor of the Bone", "Glomus Neoplasm of the Bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone Glomus Tumor", "shortest_name_length": 17}
{"curie": "MONDO:0002185", "names": ["Hyperostosis", "Hyperostoses", "HYPEROSTOSIS", "hyperostosis", "bony overgrowth", "Bone overgrowth", "Bony overgrowth", "bone hypertrophy", "Bone hypertrophy", "Bone Hypertrophy", "bone; hypertrophy", "Hypertrophy, Bone", "Hyperostosis, NOS", "hypertrophy; bone", "Bone Hypertrophies", "Hypertrophy of bone", "hypertrophy of bone", "Hypertrophies, Bone", "Hypertrophy of bone, NOS", "Hypertrophy of bone (disorder)", "hypertrophy of bone (diagnosis)", "Hypertrophy of bone, site unspecified", "Hypertrophy of bone, unspecified site", "hypertrophy of bone (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperostosis", "shortest_name_length": 12}
{"curie": "MONDO:0010540", "names": ["EBM", "HBDM", "hereditary bullous dystrophy", "bullous dystrophy, macular type", "epidermolysis bullosa macular type", "epidermolysis bullosa, macular type", "EPIDERMOLYSIS BULLOSA, MACULAR TYPE", "Epidermolysis Bullosa, Macular Type", "Hereditary macular epidermolysis bullosa", "hereditary macular epidermolysis bullosa", "epidermolysis bullosa, macular type (EBM)", "bullous dystrophy hereditary macular type", "Hereditary bullous dystrophy, macular type", "BULLOUS DYSTROPHY, HEREDITARY MACULAR TYPE", "Bullous Dystrophy, Hereditary Macular Type", "bullous dystrophy, hereditary macular type", "hereditary bullous skin dystrophy, macular type", "dystrophia bullosa hereditaria, typus maculosus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bullous dystrophy, macular type", "shortest_name_length": 3}
{"curie": "MONDO:0009364", "names": ["MDDGA1", "hard syndrome", "cod-MD syndrome", "muscle-eye-brain-POMT1 related", "POMT1-Related Muscle-Eye-Brain Disease", "Muscle Eye Brain Disease, POMT1 Related", "POMT1-Related Muscle-Eye-Brain Diseases", "Disease, POMT1-Related Muscle-Eye-Brain", "Muscle-Eye-Brain Disease, POMT1-Related", "Muscle-Eye-Brain Diseases, POMT1-Related", "hydrocephalus, agyria, and retinal dysplasia", "cerebroocular dysplasia-muscular dystrophy syndrome", "congenital muscular dystrophy-dystroglycanopathy type A1", "Walker-Warburg syndrome or muscle-eye-brain disease, POMT1-related", "WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT1-RELATED", "Walker-Warburg syndrome or muscle-eye-brain disease, Pomt1-related", "congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A1", "Congenital Muscular Dystrophy Dystroglycanopathy with Brain and Eye Anomalies, Type A1", "Congenital Muscular Dystrophy-Dystroglycanopathy with Brain and Eye Anomalies, Type A1", "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1", "Muscular Dystrophy-Dystroglycanopathy (Congenital with Brain and Eye Anomalies) Type A, 1", "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type A, 1", "Muscular Dystrophy-Dystroglycanopathy (Congenital with Brain and Eye Anomalies), Type A, 1", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH EYE AND BRAIN ANOMALIES), TYPE A, 1", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 1", "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1", "shortest_name_length": 6}
{"curie": "MONDO:0024470", "names": ["benign chondrogenic tumor", "Benign Chondrogenic Tumor", "benign tumor of cartilage", "Benign cartilage neoplasm", "Benign Tumor of Cartilage", "Benign Cartilaginous Tumor", "Cartilage neoplasms benign", "benign cartilaginous tumor", "Benign Neoplasm of Cartilage", "benign chondrogenic neoplasm", "Benign Chondrogenic Neoplasm", "Benign chondrogenic neoplasm", "benign neoplasm of cartilage", "benign tumor of the cartilage", "Benign Tumor of the Cartilage", "Benign Cartilaginous Neoplasm", "benign cartilaginous neoplasm", "chondrogenic neoplasm, benign", "benign neoplasm of the cartilage", "Benign Neoplasm of the Cartilage", "Benign chondrogenic neoplasm (disorder)", "Benign chondrogenic neoplasm of bone and articular cartilage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign chondrogenic neoplasm", "shortest_name_length": 25}
{"curie": "MONDO:0056796", "names": ["CON", "Obstructive nephropathy", "OBSTRUCTIVE NEPHROPATHY", "NEPHROPATHY OBSTRUCTIVE", "Obstructive Nephropathy", "obstructive nephropathy", "NEPHROPATHY, OBSTRUCTIVE", "obstructive; nephropathy", "nephropathy; obstructive", "Obstructive nephropathy, NOS", "Obstructive nephropathy (disorder)", "congenital obstructive nephropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "obstructive nephropathy", "shortest_name_length": 3}
{"curie": "MONDO:0100363", "names": ["genital herpes simplex type 2 infectious disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genital herpes simplex type 2 infectious disorder", "shortest_name_length": 49}
{"curie": "MONDO:0006856", "names": ["Mesothelial Tumor", "mesothelial tumor", "Mesothelial tumor", "Mesothelial tumour", "mesothelial neoplasm", "Mesothelial Neoplasm", "Mesothelial neoplasm", "Neoplasm, Mesothelial", "Mesothelial Neoplasms", "MESOTHELIAL NEOPLASMS", "Neoplasms, Mesothelial", "Mesothelial tumor morphology", "Mesothelial tumour morphology", "Mesothelial neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mesothelial neoplasm", "shortest_name_length": 17}
{"curie": "MONDO:0020287", "names": ["pulmonary artery or pulmonary branch anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary artery or pulmonary branch anomaly", "shortest_name_length": 44}
{"curie": "UMLS:C0206645", "names": ["Collagenous Fibroma", "Collagenous Fibromas", "Desmoplastic Fibroma", "OSTEOFIBROMA, BENIGN", "Desmoplastic fibroma", "Fibroma, Collagenous", "Desmoplastic Fibromas", "Fibroma, Desmoplastic", "Desmoid Tumor of Bone", "Bone Desmoplastic Fibroma", "Desmoplastic Fibroblastoma", "Fibroblastoma, Desmoplastic", "Desmoplastic Fibroblastomas", "Desmoplastic Fibroma of Bone", "desmoplastic fibroma of bone", "Osseous Desmoplastic Fibroma", "Desmoplastic Fibroma of the Bone", "desmoplastic fibroma of bone (diagnosis)", "Desmoplastic fibroma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Desmoplastic fibroma", "shortest_name_length": 19}
{"curie": "MONDO:0004808", "names": ["Breast dysplasia benign", "benign mammary dysplasia", "Benign mammary dysplasia", "Benign mammary dysplasias", "Mammary dysplasia (benign)", "Benign dysplasia of breast", "benign dysplasia of breast", "Benign mammary dysplasia, NOS", "Benign mammary gland dysplasia", "Benign mammary dysplasia (disorder)", "Unspecified benign mammary dysplasia", "benign mammary dysplasia (diagnosis)", "Benign mammary dysplasia, unspecified", "Other specified benign mammary dysplasias"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign mammary dysplasia", "shortest_name_length": 23}
{"curie": "MONDO:0010313", "names": ["MRX63", "MRX68", "XLID63", "X-linked mental retardation 63", "X-linked mental retardation 68", "MENTAL RETARDATION, X-LINKED 63", "Mental Retardation, X-Linked 63", "mental retardation, X-linked 63", "MENTAL RETARDATION, X-LINKED 68", "Mental Retardation, X-Linked 68", "mental retardation, X-linked 68", "intellectual disability, X-linked 63", "mental retardation, X-linked type 63", "intellectual disability, X-linked 68", "ACSL4-related intellectual disability", "intellectual disability, X-linked type 63", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 63", "non-syndromic X-linked intellectual disability 63", "ACSL4 non-syndromic X-linked intellectual disability", "intellectual developmental disorder, X-linked 63, X-linked dominant", "non-syndromic X-linked intellectual disability caused by mutation in ACSL4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 63", "shortest_name_length": 5}
{"curie": "MONDO:0011270", "names": ["PCAP", "HPC8", "PROSTATE CANCER, HEREDITARY, 8", "Prostate Cancer, Hereditary, 8", "prostate cancer, hereditary, 8", "Predisposing For Prostate Cancer", "PREDISPOSING FOR PROSTATE CANCER", "predisposing for prostate cancer", "prostate cancer, susceptibility to", "prostate cancer, hereditary, type 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate cancer, hereditary, 8", "shortest_name_length": 4}
{"curie": "MONDO:0003205", "names": ["Renal Pelvis Adenocarcinoma", "renal pelvis adenocarcinoma", "kidney pelvis adenocarcinoma", "Kidney Pelvis Adenocarcinoma", "Adenocarcinoma of Renal Pelvis", "adenocarcinoma of renal pelvis", "Adenocarcinoma of Kidney Pelvis", "adenocarcinoma of kidney pelvis", "adenocarcinoma of the renal pelvis", "kidney renal pelvis adenocarcinoma", "Adenocarcinoma of the Renal Pelvis", "Adenocarcinoma of the Kidney Pelvis", "adenocarcinoma of the kidney pelvis", "adenocarcinoma of the kidney Pelvis", "adenocarcinoma of renal pelvis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal pelvis adenocarcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0017624", "names": ["FHHNC", "Michellis-Castrillo syndrome", "familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis", "shortest_name_length": 5}
{"curie": "MONDO:0030007", "names": ["COXPD41", "combined oxidative phosphorylation deficiency 41", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 41"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation deficiency 41", "shortest_name_length": 7}
{"curie": "UMLS:C4055623", "names": ["A1 Hydronephrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "A1 Hydronephrosis", "shortest_name_length": 17}
{"curie": "UMLS:C0262515", "names": ["Stage IA Hodgkin Lymphoma", "Stage IA Hodgkin's Disease", "HODGKIN'S DISEASE STAGE IA", "Hodgkin's Disease Stage IA", "Hodgkin's Lymphoma Stage IA", "Stage IA Hodgkin's Lymphoma", "Ann Arbor Stage IA Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage IA Hodgkin Lymphoma", "shortest_name_length": 25}
{"curie": "MONDO:0013067", "names": ["CATC3", "CTRCT34", "FOXE3 cataract (disease)", "cataract 34 multiple types", "CATARACT 34, MULTIPLE TYPES", "cataract 34, multiple types", "autosomal recessive congenital cataract 3", "cataract, autosomal recessive congenital 3", "CATARACT, AUTOSOMAL RECESSIVE CONGENITAL 3", "Cataract, Autosomal Recessive Congenital 3", "cataract (disease) caused by mutation in FOXE3", "cataract 34 multiple types with or without microcornea", "cataract 34, multiple types, with or without microcornea", "CATARACT 34, MULTIPLE TYPES, WITH OR WITHOUT MICROCORNEA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 34 multiple types", "shortest_name_length": 5}
{"curie": "MONDO:0008079", "names": ["Npdc syndrome", "NPDC SYNDROME", "DUODENAL CARCINOID SYNDROME", "duodenal carcinoid syndrome", "Duodenal Carcinoid Syndrome", "neurofibromatosis-pheochromocytoma-duodenal carcinoid syndrome", "Neurofibromatosis-Pheochromocytoma-Duodenal Carcinoid Syndrome", "NEUROFIBROMATOSIS-PHEOCHROMOCYTOMA-DUODENAL CARCINOID SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurofibromatosis-pheochromocytoma-duodenal carcinoid syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0014306", "names": ["PAN", "VAIHS", "DADA2", "ADA2 deficiency", "vasculitis due to DADA2", "ADENOSINE DEAMINASE 2 DEFICIENCY", "Adenosine deaminase 2 deficiency", "adenosine deaminase deficiency 2", "adenosine deaminase 2 deficiency", "Adenosine Deaminase 2 Deficiency", "vasculitis due to ADA2 deficiency", "deficiency of adenosine deaminase 2", "childhood-onset polyarteritis nodosa", "Adenosine deaminase deficiency type 2", "Adenosine deaminase 2 deficiency/DAD2", "POLYARTERITIS NODOSA, CHILDHOOD-ONSET", "polyarteritis nodosa, childhood-onset", "ADA2 (adenosine deaminase 2) deficiency", "DADA2 deficiency of adenosine deaminase 2", "Adenosine deaminase 2 deficiency (disorder)", "adenosine deaminase 2 deficiency (diagnosis)", "VASCULITIS, AUTOINFLAMMATION, IMMUNODEFICIENCY, AND HEMATOLOGIC DEFECTS SYNDROME", "vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome", "VAIHS vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vasculitis due to ADA2 deficiency", "shortest_name_length": 3}
{"curie": "MONDO:0002181", "names": ["bone spur", "Exostoses", "BONE SPUR", "Bone Spur", "exostoses", "Bony spur", "Bone spur", "exostosis", "Exostosis", "EXOSTOSIS", "spurs bone", "Osteophyma", "OSTEOPHYTE", "bones spur", "Osteophyte", "Spur, Bone", "osteophyte", "Bone Spurs", "bones spurs", "Spurs, Bone", "osteophytes", "Osteophytes", "Osteophytosis", "bony spurring", "osteophytosis", "Bone spur NOS", "bony outgrowth", "Bony outgrowth", "bony exostosis", "BONY EXOSTOSIS", "bone osteophyte", "Calcar calcanei", "spur, bone; spur", "spur; spur, bone", "External exotoses", "orbital exostosis", "Exostosis disorder", "Osteophyte of bone", "swimmer's exostosis", "Exostosis - disorder", "Exostosis (disorder)", "exostosis (diagnosis)", "External hyperostosis", "bone spur (diagnosis)", "Hyperostosis, external", "Osteophyte, site unspecified", "Exostosis of unspecified site", "Osteophyte of bone (disorder)", "Osteophyte (morphologic abnormality)", "ear blockage caused by overgrown bone", "External hyperostosis (morphologic abnormality)", "Formation of new noncancerous bone on top of existing bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exostosis", "shortest_name_length": 9}
{"curie": "UMLS:C3501847", "names": ["Night blindness, congenital stationary, type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Night blindness, congenital stationary, type 1", "shortest_name_length": 46}
{"curie": "MONDO:0005983", "names": ["Favus", "favus", "Favus NOS", "Tinea Favosa", "tinea favosa", "Tinea favosa", "Favus capitis", "Tinea favosa (disorder)", "tinea favosa (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tinea favosa", "shortest_name_length": 5}
{"curie": "MONDO:0019209", "names": ["JE", "ENCEPHALITIS, SUMMER", "encephalitis Japanese", "Japanese Encephalitis", "Japanese encephalitis", "encephalitis; Japanese", "Encephalitis, Japanese", "Japanese; encephalitis", "Japanese b encephalitis", "Japanese B encephalitis", "Japanese B Encephalitis", "Encephalitis Japanese B", "ENCEPHALITIS, JAPANESE B", "Encephalitis, Japanese B", "JE - Japanese encephalitis", "JBE - Japanese B encephalitis", "Japanese B Viral Encephalitis", "Japanese B viral encephalitis", "Viral Encephalitis, Japanese B", "Russian; autumnal encephalitis", "ENCEPHALITIS, RUSSIAN AUTUMNAL", "autumnal encephalitis; Russian", "encephalitis; Russian, autumnal", "Japanese encephalitis (diagnosis)", "Japanese encephalitis virus disease", "autumnal; Russian autumnal encephalitis", "Japanese encephalitis virus disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Japanese encephalitis", "shortest_name_length": 2}
{"curie": "MONDO:0014698", "names": ["NEDHSB", "EHLMRS", "EPILEPSY, HEARING LOSS, AND MENTAL RETARDATION SYNDROME", "epilepsy, hearing loss, and mental retardation syndrome", "epilepsy, hearing loss, and intellectual disability syndrome", "neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities", "NEURODEVELOPMENTAL DISORDER WITH HEARING LOSS, SEIZURES, AND BRAIN ABNORMALITIES", "Microcephaly-intellectual disability-sensorineural deafness-epilepsy-abnormal muscle tone syndrome", "microcephaly-intellectual disability-sensorineural deafness-epilepsy-abnormal muscle tone syndrome", "Microcephaly, intellectual disability, sensorineural deafness, epilepsy, abnormal muscle tone syndrome", "microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome", "Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome", "Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome", "Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C4055504", "names": ["acquired central hypothyroidism", "Acquired central hypothyroidism", "Acquired Central Hypothyroidism", "Acquired central hypothyroidism (disorder)", "acquired central hypothyroidism (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired central hypothyroidism", "shortest_name_length": 31}
{"curie": "MONDO:0014307", "names": ["DDD4", "Dowling-Degos disease 4", "DOWLING-DEGOS DISEASE 4", "Dowling-Degos disease type 4", "POGLUT1 Dowling-Degos disease", "Dowling-Degos disease caused by mutation in POGLUT1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dowling-Degos disease 4", "shortest_name_length": 4}
{"curie": "UMLS:C2938981", "names": ["Limb asymmetry"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Limb asymmetry", "shortest_name_length": 14}
{"curie": "MONDO:0004550", "names": ["cornea melanoma", "Cornea Melanoma", "corneal melanoma", "Corneal Melanoma", "Melanoma of Cornea", "melanoma of cornea", "Melanoma of the Cornea", "melanoma of the cornea", "Malignant Cornea Melanoma", "malignant cornea melanoma", "cornea melanoma (disease)", "malignant Corneal melanoma", "malignant corneal melanoma", "Malignant Corneal Melanoma", "melanoma (disease) of cornea", "Malignant Melanoma of Cornea", "malignant melanoma of cornea", "Malignant melanoma of cornea", "Malignant Melanoma of the Cornea", "malignant melanoma of the cornea", "malignant melanoma of cornea (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant cornea melanoma", "shortest_name_length": 15}
{"curie": "MONDO:0005478", "names": ["Twisting spikes", "torsade de pointe", "TORSADE DE POINTES", "Torsade de pointes", "de pointe torsades", "des pointe torsade", "torsade de pointes", "Torsade de Pointes", "de Pointes, Torsade", "Torsades de Pointes", "torsades de pointes", "Torsades de pointes", "Torsades De Pointes", "TORSADES DE POINTES", "des pointes torsade", "Pointes, Torsade de", "des pointes torsades", "Pointes, Torsades de", "de Pointes, Torsades", "TdP ventricular tachycardia", "Torsades de pointes (disorder)", "Torsades de pointes (diagnosis)", "Torsades De Pointes by ECG Finding", "Torsades De Pointes by EKG Finding", "Ventricular tachycardia, torsades de pointes", "Ventricular tachycardia, polymorphic with Q-T prolongation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "torsades de pointes", "shortest_name_length": 15}
{"curie": "MONDO:0023099", "names": ["FRAXD", "FRAXD syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FRAXD syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C5419077", "names": ["Locally Advanced Liver Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Liver Carcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C4728213", "names": ["PROS", "PIK3CA-related overgrowth syndrome", "PIK3CA related overgrowth spectrum", "PIK3CA related overgrowth syndrome", "PIK3CA-Related Overgrowth Spectrum", "Phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha related overgrowth syndrome", "PROS - phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha related overgrowth spectrum", "Phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha related overgrowth syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PIK3CA related overgrowth spectrum", "shortest_name_length": 4}
{"curie": "MONDO:0021221", "names": ["Acoustic Nerve Tumor", "acoustic nerve tumor", "tumor of acoustic nerve", "Tumor of Acoustic Nerve", "acoustic nerve neoplasm", "Acoustic Nerve Neoplasm", "cranial nerve viii tumor", "Eighth Cranial Nerve Tumor", "neoplasm of acoustic nerve", "eighth cranial nerve tumor", "Neoplasm of acoustic nerve", "Neoplasm of Acoustic Nerve", "Tumor of VIII cranial nerve", "Tumor of the Acoustic Nerve", "tumor of the acoustic nerve", "Tumour of VIII cranial nerve", "cranial nerve eight neoplasms", "eighth cranial nerve neoplasm", "Vestibulocochlear Nerve Tumor", "Tumor of eighth cranial nerve", "Tumor of Eighth Cranial Nerve", "tumor of eighth cranial nerve", "Eighth Cranial Nerve Neoplasm", "Cranial Nerve Eight Neoplasms", "vestibulocochlear nerve tumor", "eighth cranial nerve neoplasms", "Eighth Cranial Nerve Neoplasms", "neoplasm of the acoustic nerve", "Neoplasm of the Acoustic Nerve", "Tumour of eighth cranial nerve", "tumor of vestibulocochlear nerve", "Vestibulocochlear Nerve Neoplasm", "Tumor of Vestibulocochlear Nerve", "vestibulocochlear nerve neoplasm", "Neoplasm of Eighth Cranial Nerve", "neoplasm of eighth cranial nerve", "acoustic nerve tumors vestibular", "Tumor of the Eighth Cranial Nerve", "tumor of the eighth cranial nerve", "Vestibuloacoustic Nerve Neoplasms", "Vestibulocochlear Nerve Neoplasms", "vestibulocochlear nerve neoplasms", "Vestibuloacoustic nerve neoplasms", "Neoplasm of Vestibulocochlear Nerve", "neoplasm of vestibulocochlear nerve", "tumor of the vestibulocochlear nerve", "Tumor of the Vestibulocochlear Nerve", "Neoplasm of the Eighth Cranial Nerve", "neoplasm of the eighth cranial nerve", "Neoplasm of acoustic nerve (disorder)", "neoplasm of the vestibulocochlear nerve", "Neoplasm of the Vestibulocochlear Nerve", "vestibulocochlear nerve neoplasm (disease)", "neoplasm of eighth cranial nerve (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vestibulocochlear nerve neoplasm", "shortest_name_length": 20}
{"curie": "MONDO:0005626", "names": ["epithelioma", "Epithelioma", "epithelial tumor", "Epithelial tumor", "Epithelial tumour", "epithelial tumors", "epithelial tumour", "epithelial neoplasm", "Epithelial neoplasm", "Epithelial Neoplasm", "Epithelial Neoplasms", "Neoplasm, Epithelial", "Neoplasms, Epithelial", "Epithelioma, malignant", "Epithelial Cell Neoplasm", "Epithelial Cell Neoplasms", "Cell Neoplasm, Epithelial", "Neoplasm, Epithelial Cell", "EPITHELIAL NEOPLASMS, NOS", "Epithelial Neoplasms, NOS", "Cell Neoplasms, Epithelial", "Glandular Epithelial Neoplasm", "Neoplasm, Glandular Epithelial", "Epithelial Neoplasm, Glandular", "Glandular Epithelial Neoplasms", "Neoplasms, Glandular Epithelial", "Unspecified Epithelial Neoplasms", "Glandular and Epithelial Neoplasms", "Neoplasms, Glandular and Epithelial", "Epithelioma (morphologic abnormality)", "Epithelial neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epithelial neoplasm", "shortest_name_length": 11}
{"curie": "MONDO:0019160", "names": ["PPFG", "primary progressive freezing gait", "Primary progressive freezing gait", "Primary progressive freezing gait syndrome", "Primary progressive freezing gait syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary progressive freezing gait", "shortest_name_length": 4}
{"curie": "UMLS:C1711390", "names": ["Rectosigmoid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rectosigmoid Adenocarcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C3640034", "names": ["Cervical Meningocele"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Meningocele", "shortest_name_length": 20}
{"curie": "MONDO:0012033", "names": ["PERRS", "Bradyopsia", "BRADYOPSIA", "bradyopsia", "bradyopsia 1", "Bradyopsia (disorder)", "Difficulty seeing moving objects", "Prolonged Electroretinal Response Suppression", "PROLONGED ELECTRORETINAL RESPONSE SUPPRESSION", "prolonged electroretinal response suppression", "Prolonged electroretinal response suppression", "prolonged electroretinal response suppression 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bradyopsia", "shortest_name_length": 5}
{"curie": "UMLS:C3273011", "names": ["Unclassified Hepatocellular Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unclassified Hepatocellular Adenoma", "shortest_name_length": 35}
{"curie": "MONDO:0060551", "names": ["CADEDS", "cerebellar atrophy, developmental delay, and seizures", "CEREBELLAR ATROPHY, DEVELOPMENTAL DELAY, AND SEIZURES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellar atrophy, developmental delay, and seizures", "shortest_name_length": 6}
{"curie": "UMLS:C2350171", "names": ["Bilateral Nasal Obstruction", "Obstruction, Bilateral Nasal", "Nasal Obstruction, Bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bilateral Nasal Obstruction", "shortest_name_length": 27}
{"curie": "UMLS:C5235945", "names": ["Locally Advanced Dedifferentiated Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Dedifferentiated Liposarcoma", "shortest_name_length": 45}
{"curie": "UMLS:C0263105", "names": ["ABDOMEN WALL ABSCESS", "Abdominal wall abscess", "abdominal wall abscess", "Abscess of abdominal wall", "Anterior abdominal wall abscess", "Abscess of abdominal wall (disorder)", "Abscess of abdominal wall (diagnosis)", "inflammatory disorder abscess of abdominal wall"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abscess of abdominal wall", "shortest_name_length": 20}
{"curie": "MONDO:0007183", "names": ["Azotemia, Familial", "azotemia, familial", "AZOTEMIA, FAMILIAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "azotemia, familial", "shortest_name_length": 18}
{"curie": "UMLS:C0151717", "names": ["HYPERTROPHY SKIN", "skin hypertrophy", "Skin hypertrophy", "SKIN HYPERTROPHY", "Hypertrophy skin", "hypertrophic skin", "hypertrophies skin", "hypertrophy of skin", "Hypertrophy of skin", "skin texture hypertrophic", "skin hypertrophy (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin hypertrophy", "shortest_name_length": 16}
{"curie": "UMLS:C4525203", "names": ["Stage III Hepatocellular Cancer", "Stage III Liver Cell Carcinoma AJCC v8", "Stage III Hepatocellular Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Hepatocellular Carcinoma AJCC v8", "shortest_name_length": 31}
{"curie": "UMLS:C4524725", "names": ["Pathologic Stage I Gastroesophageal Junction Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage I Gastroesophageal Junction Adenocarcinoma AJCC v8", "shortest_name_length": 67}
{"curie": "UMLS:C4054048", "names": ["Sclerosing PEComa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sclerosing PEComa", "shortest_name_length": 17}
{"curie": "UMLS:C0347630", "names": ["Liver hematoma", "liver hematoma", "hematoma liver", "Liver haematoma", "hematomas liver", "hematoma; liver", "liver; hematoma", "Hepatic hematoma", "hepatic hematoma", "Hepatic haematoma", "Liver hematoma (disorder)", "hepatic hematoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liver hematoma", "shortest_name_length": 14}
{"curie": "MONDO:0017886", "names": ["Translocation renal cell carcinoma", "translocation renal cell carcinoma", "Renal Cell Carcinoma with MiT Translocations", "MiT family translocation renal cell carcinoma", "MIT family translocation renal cell carcinoma", "carcinoma associated with MITF/TFE translocation", "Carcinoma associated with MITF/TFE translocation", "MiT family translocation renal cell carcinoma (disorder)", "MiT Family Translocation-Associated Renal Cell Carcinoma", "MiT family translocation renal cell carcinoma (diagnosis)", "renal malignant carcinoma renal cell, MiT family translocation", "MiT family translocation renal cell carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MIT family translocation renal cell carcinoma", "shortest_name_length": 34}
{"curie": "UMLS:C4727419", "names": ["Recurrent Parotid Gland Undifferentiated Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Parotid Gland Undifferentiated Carcinoma", "shortest_name_length": 50}
{"curie": "UMLS:C0948342", "names": ["citrate toxicity", "Citrate toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Citrate toxicity", "shortest_name_length": 16}
{"curie": "MONDO:0009816", "names": ["OPTB2", "osteoclast-poor osteopetrosis", "osteopetrosis osteoclast-poor", "OSTEOPETROSIS, OSTEOCLAST-POOR", "Osteopetrosis, Osteoclast-Poor", "osteopetrosis, osteoclast-poor", "osteopetrosis autosomal recessive 2", "autosomal recessive osteopetrosis 2", "osteopetrosis, autosomal recessive 2", "OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2", "Osteopetrosis, Autosomal Recessive 2", "autosomal recessive osteopetrosis type 2", "osteopetrosis, autosomal recessive type 2", "TNFSF11 autosomal recessive osteopetrosis", "mild autosomal recessive form osteopetrosis", "osteopetrosis, mild autosomal recessive form", "OSTEOPETROSIS, MILD AUTOSOMAL RECESSIVE FORM", "Osteopetrosis, mild autosomal recessive form", "Mild autosomal recessive form of osteopetrosis", "TNFSF11 autosomal recessive malignant osteopetrosis", "autosomal recessive osteopetrosis caused by mutation in TNFSF11", "autosomal recessive malignant osteopetrosis caused by mutation in TNFSF11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive osteopetrosis 2", "shortest_name_length": 5}
{"curie": "MONDO:0024387", "names": ["Sex cord stromal tumor, benign", "benign ovarian Sex cord-stromal tumor", "Benign Ovarian Sex Cord-Stromal Tumor", "benign ovarian sex cord-stromal tumor", "ovarian SEX cord-stromal tumor, benign", "benign Sex cord-stromal tumor of ovary", "ovarian sex cord-stromal tumor, benign", "Benign Sex Cord-Stromal Tumor of Ovary", "benign ovarian Sex cord-stromal neoplasm", "ovarian sex cord-stromal benign neoplasm", "Benign Ovarian Sex Cord-Stromal Neoplasm", "Benign Sex Cord-Stromal Neoplasm of Ovary", "benign Sex cord-stromal neoplasm of ovary", "Benign Sex Cord-Stromal Tumor of the Ovary", "benign Sex cord-stromal tumor of the ovary", "Benign Sex Cord-Stromal Neoplasm of the Ovary", "benign Sex cord-stromal neoplasm of the ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign ovarian sex cord-stromal tumor", "shortest_name_length": 30}
{"curie": "UMLS:C0032963", "names": ["Cardiovascular Pregnancy Complication", "Pregnancy Complication, Cardiovascular", "Cardiovascular Pregnancy Complications", "Complication, Cardiovascular Pregnancy", "Pregnancy, Cardiovascular Complications", "Complications, Cardiovascular Pregnancy", "Pregnancy Complications, Cardiovascular", "Pregnancies, Cardiovascular Complications"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pregnancy Complications, Cardiovascular", "shortest_name_length": 37}
{"curie": "MONDO:0002661", "names": ["uvea disease", "Uveal Disease", "uveal disease", "uvea disorder", "uveal diseases", "uveal disorder", "Uveal Disorder", "Uveal Diseases", "Disease, Uveal", "disease of uvea", "UVEAL DISORDERS", "Diseases, Uveal", "disorder of uvea", "uveal tract disease", "disorder of uveal tract", "Disorder of uveal tract", "uvea disease or disorder", "disease or disorder of uvea", "Disorder of uveal tract, NOS", "Disease or syndrome of uveal tract", "Disorder of uveal tract (disorder)", "disease (or disorder); uveal tract", "Diseases and Syndromes of Uveal Tract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uveal disorder", "shortest_name_length": 12}
{"curie": "MONDO:0009037", "names": ["CRANIOSYNOSTOSIS WITH ANOMALIES OF THE CRANIAL BASE AND DIGITS", "Craniosynostosis with Anomalies of the Cranial Base and Digits", "craniosynostosis with anomalies of the cranial base and digits"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniosynostosis with anomalies of the cranial base and digits", "shortest_name_length": 62}
{"curie": "UMLS:C4289045", "names": ["Gastroesophageal Junction Large Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastroesophageal Junction Large Cell Neuroendocrine Carcinoma", "shortest_name_length": 61}
{"curie": "MONDO:0003658", "names": ["gray zone lymphoma", "Grey zone lymphoma", "Gray Zone Lymphoma", "Gray zone lymphoma", "Hodgkin-Like Anaplastic Large Cell Lymphoma", "large B-cell lymphoma with Hodgkin features", "Hodgkin-like anaplastic large cell lymphoma", "Large B-Cell Lymphoma with Hodgkin Features", "B-cell lymphoma, unclassifiable, with features Intermediate between diffuse large B-cell lymphoma and Classic Hodgkin lymphoma", "B-Cell Lymphoma, Unclassifiable, with Features Intermediate between Diffuse Large B-Cell Lymphoma and Classic Hodgkin Lymphoma", "B-cell lymphoma unclassifiable with features intermediate between classical Hodgkin lymphoma and diffuse large B-cell lymphoma", "B-cell lymphoma, unclassifiable, with features Intermediate between diffuse large B-cell lymphoma and classical Hodgkin lymphoma", "B-cell lymphoma, unclassifiable, with features intermediate between diffuse large B-cell lymphoma and classical Hodgkin lymphoma", "B-Cell Lymphoma, Unclassifiable, with Features Intermediate between Diffuse Large B-Cell Lymphoma and Classical Hodgkin Lymphoma", "B-cell lymphoma, unclassifiable, with features intermediate between diffuse large b-cell lymphoma and classical Hodgkin lymphoma", "B-cell lymphoma unclassifiable with features intermediate between classical Hodgkin lymphoma and diffuse large B-cell lymphoma (disorder)", "B-cell lymphoma unclassifiable with features intermediate between classical Hodgkin lymphoma and diffuse large B-cell lymphoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-cell lymphoma, unclassifiable, with features intermediate between diffuse large b-cell lymphoma and classical Hodgkin lymphoma", "shortest_name_length": 18}
{"curie": "UMLS:C0854862", "names": ["Stage III T-Lymphoblastic Leukemia/Lymphoma", "Stage III T Lymphoblastic Leukemia/Lymphoma", "Stage III Precursor T-Lymphoblastic Lymphoma/Leukemia", "Precursor T-Lymphoblastic Lymphoma/Leukemia Stage III", "Precursor T-lymphoblastic lymphoma/leukemia stage III", "Precursor T-lymphoblastic lymphoma/leukaemia stage III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Precursor T-lymphoblastic lymphoma/leukemia stage III", "shortest_name_length": 43}
{"curie": "MONDO:0024642", "names": ["gastric NET G2", "Gastric NET G2", "Gastric Neuroendocrine Tumor G2", "gastric neuroendocrine tumor G2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric neuroendocrine tumor G2", "shortest_name_length": 14}
{"curie": "UMLS:C1334999", "names": ["Non-Neoplastic Cardiovascular Disease", "Non-Neoplastic Cardiovascular Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Cardiovascular Disorder", "shortest_name_length": 37}
{"curie": "UMLS:C1519695", "names": ["Tumor of Specialized Prostatic Stroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tumor of Specialized Prostatic Stroma", "shortest_name_length": 37}
{"curie": "MONDO:0004592", "names": ["impetigo", "IMPETIGO", "Impetigo", "Impetigos", "Impetigo NOS", "Impetigo, NOS", "Impetigo (disorder)", "Impetigo contagiosa", "Superficial pustule", "IMPETIGO CONTAGIOSA", "Impetigo Contagiosa", "impetigo (diagnosis)", "Impetigo Contagiosas", "Contagiosa, Impetigo", "Contagiosas, Impetigo", "Impetigo, unspecified", "Impetigo [any organism] [any site]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "impetigo", "shortest_name_length": 8}
{"curie": "UMLS:C5446410", "names": ["Lacrimal Gland Acinic Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lacrimal Gland Acinic Cell Carcinoma", "shortest_name_length": 36}
{"curie": "MONDO:0008642", "names": ["VATER syndrome", "VATER Syndrome", "VATER anomalad", "vater syndrome", "syndrome vater", "VATER; syndrome", "syndrome vaters", "syndrome; VATER", "VACTERL syndrome", "VACTERL Syndrome", "VATER Association", "association vater", "vater association", "VATER association", "Vater association", "association vaters", "VACTEL Association", "VACTERL Association", "VACTERL association", "VACTERL/VATER association", "VATER/VACTERL association", "VACTERL/vater association", "VATER/VACTERL ASSOCIATION", "association disorder vaters", "Vater association (diagnosis)", "Vertebral Anal Tracheoesophageal Esophageal Radial anomalies", "Vertebral defects, Anal atresia, Tracheoesophageal fistula with Esophageal atresia, and Radial dysplasia", "vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, renal anomalies, limb defects syndrome", "Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, renal anomalies, limb defects syndrome", "vertebral abnormalities, anal atresia, Cardiac abnormalities, tracheo-esophageal fistula, renal anomalies, limb defects syndrome", "Vertebral Abnormalities, Anal Atresia, Cardiac Abnormalities, Tracheo-Esophageal Fistula, Renal Anomalies, Limb Defects Syndrome", "Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-oesophageal fistula, renal anomalies, limb defects syndrome", "Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, renal anomalies, limb defects (VACTERL) syndrome", "Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, renal anomalies, limb defects syndrome (disorder)", "Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-oesophageal fistula, renal anomalies, limb defects (VACTERL) syndrome", "Vertebral anomalies/dysgenesis, anal atresia, tracheo-esophageal fistula, esophageal atresia, renal anomalies, radial dysplasia association", "vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, renal anomalies, limb defects syndrome (diagnosis)", "Vertebral anomalies/dysgenesis, anal atresia, tracheo-oesophageal fistula, oesophageal atresia, renal anomalies, radial dysplasia association", "Vertebral anomalies/dysgenesis, anal atresia, tracheo-esophageal fistula, esophageal atresia, renal anomalies, radial dysplasia (VATER) association", "Vertebral anomalies/dysgenesis, anal atresia, tracheo-oesophageal fistula, oesophageal atresia, renal anomalies, radial dysplasia (VATER) association", "Vertebral anomalies/dysgenesis, anal atresia, tracheo-esophageal fistula, esophageal atresia, renal anomalies, radial dysplasia association (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "VACTERL/vater association", "shortest_name_length": 14}
{"curie": "UMLS:C0155165", "names": ["Conjunctival Granuloma", "granuloma; conjunctiva", "conjunctival granuloma", "conjunctiva; granuloma", "Conjunctival granuloma", "Granuloma of Conjunctiva", "Granuloma of conjunctiva", "conjunctival granuloma (diagnosis)", "Granuloma of conjunctiva (disorder)", "Conjunctival granuloma, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Granuloma of conjunctiva", "shortest_name_length": 22}
{"curie": "MONDO:0019782", "names": ["humero-ulnar fusion", "humero-ulnar synostosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "humero-ulnar synostosis", "shortest_name_length": 19}
{"curie": "UMLS:C0272316", "names": ["Hereditary coagulation factor deficiency", "Hereditary Coagulation Factor Deficiency", "Hereditary coagulation factor deficiency, NOS", "Hereditary coagulation factor deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hereditary coagulation factor deficiency", "shortest_name_length": 40}
{"curie": "MONDO:0024636", "names": ["CARDITIS", "carditis", "Carditis", "Carditis (disorder)", "carditis (diagnosis)", "heart layer inflammation", "inflammation of heart layer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammation of heart layer", "shortest_name_length": 8}
{"curie": "UMLS:C4726542", "names": ["Myeloid Neoplasms with Germline DDX41 Mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myeloid Neoplasms with Germline DDX41 Mutation", "shortest_name_length": 46}
{"curie": "UMLS:C1336063", "names": ["Splenic Manifestation of CML", "Splenic Manifestation of Chronic Myelogenous Leukemia", "Splenic Manifestation of Chronic Myelogenous Leukemia, BCR-ABL1 Positive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Splenic Manifestation of Chronic Myelogenous Leukemia, BCR-ABL1 Positive", "shortest_name_length": 28}
{"curie": "MONDO:0020689", "names": ["ADC", "HIV dementia", "dementia HIV", "HIV Dementia", "Dementia, HIV", "AIDS Dementia", "AIDS dementia", "AIDS DEMENTIA", "dementia AIDS", "HIV Dementias", "Dementias, HIV", "HIV encephalitis", "HIV Encephalopathy", "Encephalopathy, HIV", "AIDS Encephalopathy", "Encephalopathy, AIDS", "HIV-related dementia", "hiv-related dementia", "HIV Encephalopathies", "aids-related dementia", "AIDS Encephalopathies", "AIDS-related dementia", "Encephalopathies, HIV", "aids dementia complex", "AIDS Dementia Complex", "AIDS-dementia complex", "AIDS dementia complex", "Aids dementia complex", "Complex, AIDS Dementia", "Encephalopathies, AIDS", "Dementia Complex, AIDS", "AIDS with dementia, NOS", "HIV-associated dementia", "AIDS RELAT DEMENTIA COMPLEX", "Dementia due to HIV disease", "DEMENTIA COMPLEX AIDS RELAT", "Dementia associated with AIDS", "AIDS with dementia (disorder)", "AIDS-related Dementia Complex", "AIDS related Dementia Complex", "AIDS Related Dementia Complex", "AIDS-Related Dementia Complex", "Dementia Complex, AIDS related", "Dementia Complex, AIDS-related", "Complex, AIDS-Related Dementia", "Dementia Complex, AIDS Related", "Dementia Complex, AIDS-Related", "Complex, AIDS-related Dementia", "HIV disease; dementia (etiology)", "HIV 1 Cognitive and Motor Complex", "HIV-1 Cognitive and Motor Complex", "AIDS related cognitive impairment", "HIV ASSOC COGNITIVE MOTOR COMPLEX", "HIV disease; dementia (manifestation)", "HIV Associated Cognitive Motor Complex", "HIV-Associated Cognitive Motor Complex", "HIV associated cognitive motor complex", "HIV-1-Associated Cognitive Motor Complex", "HIV 1 Associated Cognitive Motor Complex", "HIV associated cognitive and motor complex", "HIV disease; resulting in, dementia (etiology)", "DEMENTIA COMPLEX ACQUIRED IMMUNE DEFIC SYNDROME", "Dementia with acquired immunodeficiency syndrome", "acquired immunodeficiency syndrome (AIDS) dementia", "HIV disease; resulting in, dementia (manifestation)", "Acquired-Immune Deficiency Syndrome Dementia Complex", "acquired immune deficiency syndrome dementia complex", "Acquired immune deficiency syndrome dementia complex", "acquired immune deficiency syndrome-related dementia", "Acquired immune deficiency syndrome-related dementia", "Dementia Complex, Acquired Immune Deficiency Syndrome", "Dementia in human immunodeficiency virus [HIV] disease", "Dementia with AIDS (acquired immunodeficiency syndrome)", "dementia; human immunodeficiency virus disease (etiology)", "AIDS (acquired immunodeficiency syndrome) dementia complex", "ADC - Acquired immune deficiency syndrome dementia complex", "AIDS - Acquired immune deficiency syndrome dementia complex", "Dementia with acquired immunodeficiency syndrome (disorder)", "Dementia associated with acquired immunodeficiency syndrome", "dementia; human immunodeficiency virus disease (manifestation)", "acquired immunodeficiency syndrome (AIDS) dementia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS dementia complex", "shortest_name_length": 3}
{"curie": "MONDO:0022401", "names": ["agyria pachygyria polymicrogyria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "agyria pachygyria polymicrogyria", "shortest_name_length": 32}
{"curie": "MONDO:0023605", "names": ["LHS", "Laugier-Hunziker syndrome", "Laugier and Hunziker pigmentation", "Laugier-Hunziker syndrome (disorder)", "Laugier-Hunziker syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laugier-Hunziker syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C0577709", "names": ["Proteus urinary tract infection", "URINARY TRACT INFECTION PROTEUS", "Proteus UTI (urinary tract infection)", "urinary tract infection due to Proteus", "Proteus urinary tract infection (disorder)", "urinary tract infection due to Proteus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Proteus urinary tract infection", "shortest_name_length": 31}
{"curie": "MONDO:0044875", "names": ["CMD", "Syndrome X", "syndrome X", "syndrome x", "Angina X Syndrome", "Angina Syndrome X", "Cardiac Syndrome X", "Angina X Syndromes", "Syndrome, Angina X", "Cardiac syndrome X", "Angina Syndrome Xs", "Syndrome X, Angina", "X Syndrome, Angina", "cardiac syndrome x", "Syndrome Xs, Angina", "Syndrome X, Cardiac", "Syndrome X (Cardiac)", "Microvascular angina", "microvascular angina", "Microvascular Angina", "Angina, Microvascular", "endothelial dysfunction", "Endothelial dysfunction", "dysfunction endothelial", "dysfunctions endothelial", "Cardiac syndrome X (finding)", "Coronary small artery disease", "Coronary Microvascular Disease", "Coronary microvascular disease", "coronary microvascular disease", "coronary microvascular disorder", "microvascular endothelium heart disease", "Impaired flow-mediated arterial dilatation", "heart disease of microvascular endothelium", "Chest pain with normal coronary angiography", "Angina Pectoris with Normal Coronary Arteriogram"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coronary microvascular disorder", "shortest_name_length": 3}
{"curie": "MONDO:0004977", "names": ["AILT", "AILD", "AITL", "aild", "lymphogranulomatosis X", "Lymphogranulomatosis X", "T-cell lymphoma, AILD type", "Angioimmunoblastic lymphoma", "angioimmunoblastic lymphoma", "Angioblastic lymphadenopathy", "angioblastic lymphadenopathy", "lymphoma; angioimmunoblastic", "angioimmunoblastic; lymphoma", "immunoblastic lymphadenopathy", "Immunoblastic Lymphadenopathy", "Immunoblastic lymphadenopathy", "Lymphadenopathy, immunoblastic", "Lymphadenopathy, Immunoblastic", "LYMPHADENOPATHY, IMMUNOBLASTIC", "Immunoblastic Lymphadenopathies", "Lymphadenopathies, Immunoblastic", "Angioimmunoblastic T-cell lymphoma", "angioimmunoblastic lymphadenopathy", "ANGIOIMMUNOBLASTIC LYMPHADENOPATHY", "Angioimmunoblastic Lymphadenopathy", "Angioimmunoblastic lymphadenopathy", "angioimmunoblastic T-cell lymphoma", "Angioimmunoblastic T-Cell Lymphoma", "Angioimmunoblastic T-cell lymphomas", "Angio-immunoblastic lymphadenopathy", "angioimmunoblastic; lymphadenopathy", "Lymphadenopathy, Angioimmunoblastic", "lymphadenopathy; angioimmunoblastic", "Angioimmunoblastic Lymphadenopathies", "Lymphadenopathies, Angioimmunoblastic", "Angioimmunoblastic T-cell lymphoma NOS", "malignant immunoblastic lymphadenopathy", "angioimmunoblastic lymphadenopathy (AILD)", "Angioimmunoblastic T-cell lymphoma (disorder)", "angioimmunoblastic T-cell lymphoma (diagnosis)", "malignant angioimmunoblastic lymphadenopathy (AILD)", "malignant immunoblastic lymphadenopathy (diagnosis)", "angioimmunoblastic lymphadenopathy with Dysproteinemia", "Angioimmunoblastic Lymphadenopathy with Dysproteinemia", "angioimmunoblastic lymphadenopathy with dysproteinemia", "Angioimmunoblastic lymphadenopathy with dysproteinemia", "angioimmunoblastic lymphadenopathy type T-cell lymphoma", "Angioimmunoblastic Lymphadenopathy Type T-Cell Lymphoma", "Angioimmunoblastic lymphadenopathy with dysproteinaemia", "LYMPHADENOPATHY, ANGIOIMMUNOBLASTIC, WITH DYSPROTEINEMIA", "Angioimmunoblastic T-cell lymphoma (morphologic abnormality)", "Angioimmunoblastic lymphadenopathy (morphologic abnormality)", "Angioimmunoblastic lymphadenopathy with dysproteinemia (AILD)", "angioimmunoblastic lymphadenopathy with dysproteinemia (AILD)", "Peripheral T-cell lymphoma, AILD (angioimmunoblastic lymphadenopathy with dysproteinemia)", "Peripheral T-cell lymphoma, AILD (Angioimmunoblastic Lymphadenopathy with Dysproteinemia)", "Peripheral T-cell lymphoma, AILD (Angioimmunoblastic Lymphadenopathy with Dysproteinaemia)", "Peripheral T-cell lymphoma, AILD (angioimmunoblastic lymphadenopathy with dysproteinaemia)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angioimmunoblastic T-cell lymphoma", "shortest_name_length": 4}
{"curie": "UMLS:C1335334", "names": ["Paraganglioma-Like Dermal Melanocytic Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paraganglioma-Like Dermal Melanocytic Tumor", "shortest_name_length": 43}
{"curie": "UMLS:C4520717", "names": ["stage III anal cancer", "Stage III Anal Canal Cancer", "Stage III Anal Canal Cancer AJCC v6", "Stage III Anal Canal Cancer AJCC v7", "Stage III Anal Carcinoma AJCC v6 and v7", "Stage III Anal Canal Cancer AJCC v6 and v7", "Stage III Anal Canal Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Anal Canal Cancer AJCC v6 and v7", "shortest_name_length": 21}
{"curie": "MONDO:0013924", "names": ["OI13", "OI, type 13", "OI, TYPE XIII", "BMP1 osteogenesis imperfecta", "osteogenesis imperfecta type 13", "osteogenesis imperfecta, type 13", "osteogenesis imperfecta type XIII", "OSTEOGENESIS IMPERFECTA, TYPE XIII", "osteogenesis imperfecta, type XIII", "osteogenesis imperfecta caused by mutation in BMP1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteogenesis imperfecta type 13", "shortest_name_length": 4}
{"curie": "MONDO:0011702", "names": ["CMD1L", "dilated cardiomyopathy 1L", "CARDIOMYOPATHY, DILATED, 1L", "Cardiomyopathy, Dilated, 1l", "cardiomyopathy, dilated, 1L", "dilated cardiomyopathy type 1L", "cardiomyopathy, dilated, type 1L", "SGCD familial isolated dilated cardiomyopathy", "familial isolated dilated cardiomyopathy caused by mutation in SGCD"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1L", "shortest_name_length": 5}
{"curie": "MONDO:0012308", "names": ["JS-R", "JBTS4", "Joubert Syndrome 4", "Joubert syndrome 4", "JOUBERT SYNDROME 4", "Joubert syndrome type 4", "JOUBERT SYNDROME 4 (disorder)", "Joubert syndrome with renal defect", "Joubert syndrome with renal anomalies", "Joubert syndrome with renal defect (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome with renal defect", "shortest_name_length": 4}
{"curie": "MONDO:0010227", "names": ["RP3", "RP15", "RETINITIS PIGMENTOSA 3", "Retinitis Pigmentosa 3", "retinitis pigmentosa 3", "RETINITIS PIGMENTOSA 15", "retinitis pigmentosa 15", "Retinitis Pigmentosa 15", "RPGR retinitis pigmentosa", "retinitis pigmentosa type 3", "cone-rod Degeneration, X-linked", "Cone-Rod Degeneration, X-Linked", "CONE-ROD DEGENERATION, X-LINKED", "retinitis pigmentosa caused by mutation in RPGR", "Choroidoretinal Degeneration with retinal reflex in heterozygous Women", "Choroidoretinal Degeneration with Retinal Reflex in Heterozygous Women", "CHOROIDORETINAL DEGENERATION WITH RETINAL REFLEX IN HETEROZYGOUS WOMEN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 3", "shortest_name_length": 3}
{"curie": "UMLS:C5418903", "names": ["Advanced Platinum-Resistant Malignant Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Platinum-Resistant Malignant Germ Cell Tumor", "shortest_name_length": 53}
{"curie": "UMLS:C0520729", "names": ["Subconjunctival cyst", "Subconjunctival cyst (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subconjunctival cyst", "shortest_name_length": 20}
{"curie": "UMLS:C4763882", "names": ["Enteropathogenic E coli Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Enteropathogenic E coli Infection", "shortest_name_length": 33}
{"curie": "MONDO:0016789", "names": ["pyruvate metabolism disorder", "inborn error of pyruvate metabolic process", "inborn pyruvate metabolic process disorder", "rare inborn error of pyruvate metabolic process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyruvate metabolism disorder", "shortest_name_length": 28}
{"curie": "MONDO:0002075", "names": ["Spontaneous tension pneumothorax", "pneumothorax tension spontaneous", "Pneumothorax spontaneous tension", "spontaneous tension pneumothorax", "Spontaneous tension pneumothorax (disorder)", "Spontaneous tension pneumothorax (diagnosis)", "spontaneous; pneumothorax, tension pneumothorax", "pneumothorax; spontaneous, tension pneumothorax"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spontaneous tension pneumothorax", "shortest_name_length": 32}
{"curie": "UMLS:C1332347", "names": ["ADH", "DIN 1B", "Atypical Ductal Hyperplasia", "Atypical ductal hyperplasia", "atypical ductal hyperplasia", "Hyperplasia, Atypical Ductal", "Ductal Hyperplasia, Atypical", "Atypical Ductal Hyperplasias", "Ductal Hyperplasias, Atypical", "Hyperplasias, Atypical Ductal", "Atypical mammary duct hyperplasia", "atypical ductal breast hyperplasia", "Breast Atypical Ductal Hyperplasia", "Atypical Ductal Breast Hyperplasia", "Atypical Breast Ductal Hyperplasia", "Atypical ductal hyperplasia of breast", "Atypical Ductal Hyperplasia of Breast", "atypical ductal hyperplasia of breast", "atypical hyperplasia of lactiferous duct", "Atypical hyperplasia of lactiferous duct", "Atypical Ductal Hyperplasia of the Breast", "Ductal Intraepithelial Neoplasia, Grade 1B", "atypical ductal hyperplasia of breast (diagnosis)", "Atypical hyperplasia of lactiferous duct (disorder)", "atypical hyperplasia of lactiferous duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypical Ductal Breast Hyperplasia", "shortest_name_length": 3}
{"curie": "UMLS:C0520817", "names": ["physical handicap", "Physical handicap", "handicaps physical", "Physical disability", "disability physical", "Disability;physical", "physical disability", "disabilities physical", "Physical handicap (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Physical disability", "shortest_name_length": 17}
{"curie": "MONDO:0016086", "names": ["haglund's", "Kohler disease", "Kohler's disease", "osteochondrosis; foot", "foot; osteochondrosis", "Osteochondrosis of foot", "navicular Osteochondrosis", "Osteochondrosis of Haglund", "haglund's; osteochondrosis", "osteochondrosis; haglund's", "Osteochondrosis of foot NOS", "osteochondrosis; juvenile, foot", "Juvenile osteochondrosis of foot", "juvenile osteochondrosis of foot", "Osteochondrosis of the tarsal bone", "aseptic necrosis of the tarsal bone", "Juvenile osteochondrosis of foot NOS", "Juvenile osteochondrosis of the foot", "Juvenile osteochondrosis of foot, NOS", "Kohler's disease of the tarsal navicular", "osteochondritis of tarsal/metatarsal bone", "juvenile osteochondrosis of foot (diagnosis)", "Juvenile osteochondrosis of the foot (disorder)", "Kohler's Osteochondrosis of the tarsal navicular"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteochondritis of tarsal/metatarsal bone", "shortest_name_length": 9}
{"curie": "MONDO:0005145", "names": ["sporatic amyotrophic lateral sclerosis", "sporadic amyotrophic lateral sclerosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sporadic amyotrophic lateral sclerosis", "shortest_name_length": 38}
{"curie": "MONDO:0003051", "names": ["non specific chronic endometritis", "Non Specific Chronic Endometritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non specific chronic endometritis", "shortest_name_length": 33}
{"curie": "UMLS:C3640091", "names": ["Arterial Thrombosis Related to Vascular Access Complication", "Acquired Secondary Arterial Thrombosis due to Catheter Complication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arterial Thrombosis Related to Vascular Access Complication", "shortest_name_length": 59}
{"curie": "UMLS:C4054344", "names": ["Non-Functioning PitNET/Macroadenoma", "Nonfunctional Pituitary Macroadenoma", "Nonfunctional Pituitary Gland Macroadenoma", "Nonfunctioning Pituitary Gland Macroadenoma", "Non-Functioning Pituitary Gland Macroadenoma", "Non-Functioning Pituitary Neuroendocrine Tumor/Macroadenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Functioning Pituitary Neuroendocrine Tumor/Macroadenoma", "shortest_name_length": 35}
{"curie": "UMLS:C1335697", "names": ["Recurrent Central Nervous System Neoplasm", "Recurrent Childhood Central Nervous System Tumor", "Recurrent Childhood Central Nervous System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Central Nervous System Neoplasm", "shortest_name_length": 41}
{"curie": "MONDO:0015340", "names": ["dress syndrome", "drug reaction eosinophilic systemic syndrome", "drug rash with eosinophilia and systemic symptoms"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "drug rash with eosinophilia and systemic symptoms", "shortest_name_length": 14}
{"curie": "MONDO:0004009", "names": ["renal pelvis sarcomatoid transitional cell carcinoma", "Kidney Pelvis Sarcomatoid Transitional Cell Carcinoma", "kidney pelvis sarcomatoid transitional cell carcinoma", "sarcomatoid transitional cell carcinoma of renal Pelvis", "sarcomatoid transitional cell carcinoma of renal pelvis", "Sarcomatoid Transitional Cell Carcinoma of Renal Pelvis", "sarcomatoid transitional cell carcinoma of kidney pelvis", "Sarcomatoid Transitional Cell Carcinoma of Kidney Pelvis", "Sarcomatoid Transitional Cell Carcinoma of the Renal Pelvis", "sarcomatoid transitional cell carcinoma of the renal pelvis", "sarcomatoid transitional cell carcinoma of the kidney pelvis", "Sarcomatoid Transitional Cell Carcinoma of the Kidney Pelvis", "infiltrating renal pelvis urothelial carcinoma, sarcomatoid variant", "Infiltrating Renal Pelvis Urothelial Carcinoma, Sarcomatoid Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kidney pelvis sarcomatoid transitional cell carcinoma", "shortest_name_length": 52}
{"curie": "MONDO:0014006", "names": ["SHMS", "MRD17", "PACS1-related syndrome", "Schuurs-Hoeijmakers syndrome", "SCHUURS-HOEIJMAKERS SYNDROME", "Schuurs-Hoeijmakers Syndrome", "autosomal dominant mental retardation 17", "mental retardation, autosomal dominant 17", "autosomal dominant intellectual disability 17", "autosomal dominant intellectual disability-17", "intellectual disability, autosomal dominant 17", "mental retardation, autosomal dominant type 17", "intellectual disability, autosomal dominant type 17", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 17", "intellectual disability-craniofacial dysmorphism-cryptorchidism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Schuurs-Hoeijmakers syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0016706", "names": ["Chordoid glioma", "Chordoid Glioma", "chordoid glioma", "Chordoid glioma (disorder)", "third ventricle chordoid glioma", "Third Ventricle Chordoid Glioma", "Chordoid Glioma of 3rd Ventricle", "Chordoid glioma of 3rd Ventricle", "chordoid glioma of 3rd ventricle", "Chordoid glioma of third ventricle", "chordoid glioma of third ventricle", "Chordoid Glioma of Third Ventricle", "Chordoid Glioma of the 3rd Ventricle", "chordoid glioma of the 3rd ventricle", "chordoid glioma of the third ventricle", "Chordoid Glioma of the Third Ventricle", "Chordoid glioma (morphologic abnormality)", "chordoid glioma (morphologic abnormality)", "Chordoid Glioma of the Third Ventricle (WHO Grade 2)", "Chordoid Glioma of the Third Ventricle (WHO Grade II)", "chordoid glioma of the third ventricle (WHO grade II)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chordoid glioma of the third ventricle", "shortest_name_length": 15}
{"curie": "UMLS:C1947920", "names": ["Fibroelastic Papilloma", "Papillary Fibroelastoma", "Papillary fibroelastoma", "Giant Lambl Excrescence", "Papillary Fibroelastomas", "Fibroelastoma, Papillary", "Cardiac Papillary Fibroelastoma", "cardiac papillary fibroelastoma", "Cardiac papillary fibroelastoma", "Papillary fibroelastoma of heart", "Fibroelastoma, Cardiac Papillary", "Papillary Fibroelastoma, Cardiac", "papillary fibroelastoma of heart", "Cardiac Papillary Fibroelastomas", "Papillary fibroelastoma (disorder)", "Papillary fibroelastoma of heart (disorder)", "papillary fibroelastoma of heart (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiac Papillary Fibroelastoma", "shortest_name_length": 22}
{"curie": "MONDO:0000346", "names": ["Balkan hemorrhagic fever", "Hantavirus hemorrhagic fever with renal syndrome, Dobrava-Belgrade virus type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hantavirus hemorrhagic fever with renal syndrome, Dobrava-Belgrade virus type", "shortest_name_length": 24}
{"curie": "MONDO:0007663", "names": ["GLAUCOMA WITH ELEVATED EPISCLERAL VENOUS PRESSURE", "Glaucoma with Elevated Episcleral Venous Pressure", "glaucoma with elevated episcleral venous pressure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glaucoma with elevated episcleral venous pressure", "shortest_name_length": 49}
{"curie": "MONDO:0006518", "names": ["sporadic Creutzfeld Jacob disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sporadic Creutzfeld Jacob disease", "shortest_name_length": 33}
{"curie": "UMLS:C0235847", "names": ["HYPERHEMOGLOBINEMIA", "Hyperhemoglobinemia", "Hyperhaemoglobinaemia", "HYPERHAEMOGLOBINAEMIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyperhaemoglobinaemia", "shortest_name_length": 19}
{"curie": "UMLS:C0155555", "names": ["Acute rheumatic pericarditis", "Pericarditis;rheumatic;acute", "Acute Rheumatic Pericarditis", "acute rheumatic pericarditis", "Rheumatic pericarditis, acute", "acute; pericarditis, rheumatic", "pericarditis; acute, rheumatic", "Rheumatic pericarditis (acute)", "Acute Rheumatic fever with pericarditis", "Acute rheumatic fever with pericarditis", "rheumatic fever; in pericarditis, active", "Active rheumatic fever with pericarditis", "Active Rheumatic fever with pericarditis", "acute rheumatic pericarditis (diagnosis)", "pericarditis; with rheumatic fever, active", "Acute rheumatic fever with pericarditis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute rheumatic pericarditis", "shortest_name_length": 28}
{"curie": "MONDO:0010230", "names": ["MRX23", "XLID23", "X-linked mental retardation 23", "MENTAL RETARDATION, X-LINKED 23", "mental retardation, X-linked 23", "Mental Retardation, X-Linked 23", "intellectual disability, X-linked 23", "X-linked mental retardation 23 (MRX23, XLMR23)", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 23", "non-syndromic X-linked intellectual disability 23"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 23", "shortest_name_length": 5}
{"curie": "UMLS:C4682799", "names": ["Stage I Testicular Cancer", "Stage I Testicular Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Testicular Cancer AJCC v8", "shortest_name_length": 25}
{"curie": "MONDO:0060670", "names": ["ALS25", "AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 25", "amyotrophic lateral sclerosis, susceptibility to, 25"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyotrophic lateral sclerosis, susceptibility to, 25", "shortest_name_length": 5}
{"curie": "MONDO:0013800", "names": ["EDSKMH", "EDSKSCL2", "kEDS-FKBP14", "FKBP14-related EDS", "FKBP22-deficient EDS", "EDS, kyphoscoliotic and hearing loss type", "Kyphoscoliotic EDS due to FKBP22 deficiency", "Ehlers-Danlos syndrome, kyphoscoliotic type, 2", "EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2", "Ehlers-Danlos syndrome kyphoscoliotic and deafness type", "Ehlers-Danlos syndrome, kyphoscoliotic and deafness type", "Ehlers-Danlos syndrome kyphoscoliotic and hearing loss type", "EDS with progressive kyphoscoliosis, myopathy, and deafness", "Ehlers-Danlos syndrome, kyphoscoliotic and hearing loss type", "Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency", "EDS with progressive kyphoscoliosis, myopathy, and hearing loss", "Ehlers-Danlos syndrome kyphoscoliotic and deafness type (disorder)", "Ehlers-Danlos syndrome with kyphoscoliosis, myopathy, and deafness", "Ehlers-Danlos syndrome with kyphoscoliosis, myopathy, and hearing loss", "Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and deafness", "EHLERS-DANLOS SYNDROME WITH PROGRESSIVE KYPHOSCOLIOSIS, MYOPATHY, AND HEARING LOSS", "Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ehlers-Danlos syndrome, kyphoscoliotic and deafness type", "shortest_name_length": 6}
{"curie": "MONDO:0001604", "names": ["Lagopthalmos", "lagophthalmos", "Lagophthalmos", "Eyelids stay open", "Lagophthalmos, NOS", "Poor closure eyelids", "Defective lid closure", "Eyelids unable to close", "Lagophthalmos (finding)", "lagophthalmos (diagnosis)", "Incomplete closure of lid", "EYELID CLOSING IMPAIRMENT", "Unspecified lagophthalmos", "Lagophthalmos, unspecified", "lagophthalmos was observed", "Inability to close the eyelids", "lagophthalmos (physical finding)", "Lagophthalmia (incomplete closure of eyelids)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lagophthalmos", "shortest_name_length": 12}
{"curie": "UMLS:C0016665", "names": ["Fracture nonunion", "fracture nonunion", "nonunion fracture", "Ununited Fracture", "Fracture non-union", "Fracture;non-union", "fracture non union", "non union fracture", "fracture non-union", "Ununited Fractures", "Fracture, ununited", "UNUNITED FRACTURES", "fracture; nonunion", "Fracture, nonunion", "fractures nonunion", "Fracture, Ununited", "nonunion; fracture", "non-union fracture", "fractures non union", "Fractures, Ununited", "Nonunion of fracture", "of fracture nonunion", "nonunion of fracture", "union; fracture, failed", "Fracture, nonunion, NOS", "Fracture, ununited, NOS", "FRACTURE, NOS WITH NONUNION", "Nonunion of fracture (disorder)", "nonunion of fracture (diagnosis)", "Fracture, ununited (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fractures, Ununited", "shortest_name_length": 17}
{"curie": "MONDO:0033658", "names": ["NEDSEBA", "NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND BRAIN ATROPHY", "neurodevelopmental disorder with seizures and brain atrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with seizures and brain atrophy", "shortest_name_length": 7}
{"curie": "MONDO:0018113", "names": ["isolated plagiocephaly", "synostotic plagiocephaly", "non-syndromic unicoronal synostosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated plagiocephaly", "shortest_name_length": 22}
{"curie": "MONDO:0018480", "names": ["esophageal carcinoma, salivary gland type", "carcinoma of esophagus, salivary gland type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma of esophagus, salivary gland type", "shortest_name_length": 41}
{"curie": "UMLS:C3661525", "names": ["Autosomal Recessive Chronic Granulomatous Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Autosomal Recessive Chronic Granulomatous Disease", "shortest_name_length": 49}
{"curie": "MONDO:0013229", "names": ["bathing epilepsy", "Bathing epilepsy", "Aquagenic epilepsy", "hot water epilepsy", "epilepsy, hot water", "water immersion epilepsy", "epilepsy reflex aquagenic", "hot water reflex epilepsy", "Immersion-related epilepsy", "Immersion Related Epilepsy", "Epilepsy, Immersion Related", "Immersion Related Epilepsies", "Aquagenic epilepsy (disorder)", "Epilepsies, Immersion Related", "Aquagenic epilepsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hot water reflex epilepsy", "shortest_name_length": 16}
{"curie": "MONDO:0027407", "names": ["KLEFS1", "9qSTDS", "9q-syndrome", "monosomy 9q", "9q- SYNDROME", "9q- syndrome", "9q- Syndrome", "del(9q) syndrome", "Kleefstra Syndrome", "Kleefstra syndrome", "partial monosomy 9q", "9q deletion syndrome", "Kleefstra syndrome 1", "deletion 9q syndrome", "KLEEFSTRA SYNDROME 1", "chromosome 9q monosomy", "9q34.3 Deletion Syndrome", "9q34.3 Microdeletion Syndrome", "Kleefstra syndrome (disorder)", "Kleefstra syndrome (diagnosis)", "chromosome 9q deletion syndrome", "9q Subtelomeric Deletion Syndrome", "9q SUBTELOMERIC DELETION SYNDROME", "9q subtelomeric deletion syndrome", "CHROMOSOME 9q34.3 DELETION SYNDROME", "chromosome 9q34.3 deletion syndrome", "Chromosome 9q34.3 Deletion Syndrome", "Kleefstra syndrome due to del(9)(q34)", "Kleefstra syndrome due to monosomy 9q34", "Kleefstra syndrome due to 9q34 microdeletion", "Kleefstra syndrome due to 9q subtelomeric deletion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kleefstra syndrome 1", "shortest_name_length": 6}
{"curie": "UMLS:C0751849", "names": ["Right Middle Cerebral Artery Infarction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Right Middle Cerebral Artery Infarction", "shortest_name_length": 39}
{"curie": "MONDO:0022715", "names": ["Arnold Chiari type 3", "Chiari malformation type 3", "Chiari malformation type III", "type III Chiari malformation", "Chiari type III malformation", "Arnold-Chiari Malformation, Type 3", "Arnold Chiari Malformation, Type 3", "Arnold-Chiari malformation type III", "Arnold Chiari malformation type III", "Type III Arnold-Chiari Malformation", "Type III Arnold Chiari Malformation", "Arnold-Chiari type III malformation", "type III Arnold-Chiari malformation", "Arnold-Chiari Malformation, Type III", "Arnold Chiari Malformation, Type III", "Chiari malformation type III (disorder)", "type III Chiari malformation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chiari malformation type 3", "shortest_name_length": 20}
{"curie": "UMLS:C0936263", "names": ["Cerebral Thrombus", "Thrombus, Cerebral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebral Thrombus", "shortest_name_length": 17}
{"curie": "UMLS:C5239396", "names": ["Distal Cholangiocarcinoma", "Distal Bile Duct Adenocarcinoma", "Adenocarcinoma of the Distal Common Bile Duct"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Distal Bile Duct Adenocarcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0018515", "names": ["Rectal Squamous Carcinoma", "rectal squamous carcinoma", "Rectal Squamous Cell Cancer", "rectal squamous cell cancer", "Squamous Carcinoma of Rectum", "squamous carcinoma of rectum", "rectal squamous cell carcinoma", "rectum squamous cell carcinoma", "Rectal squamous cell carcinoma", "Rectal Squamous Cell Carcinoma", "squamous carcinoma of the rectum", "Squamous Carcinoma of the Rectum", "Squamous cell carcinoma of rectum", "Squamous Cell Carcinoma of Rectum", "squamous cell carcinoma of rectum", "squamous cell carcinoma of the rectum", "Squamous cell carcinoma of the rectum", "Squamous Cell Carcinoma of the Rectum", "Squamous cell carcinoma of rectum (disorder)", "squamous cell carcinoma of rectum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "squamous cell carcinoma of rectum", "shortest_name_length": 25}
{"curie": "MONDO:0011508", "names": ["NHL", "non-Hodgkin lymphoma", "NON-HODGKIN LYMPHOMA", "lymphoma, non-Hodgkin", "lymphoma, follicular, somatic", "familial non-Hodgkin lymphoma", "lymphoma, non-Hodgkin, somatic", "lymphoma, non-Hodgkin, familial", "Lymphoma, Non-Hodgkin, Familial", "LYMPHOMA, NON-HODGKIN, FAMILIAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphoma, non-Hodgkin, familial", "shortest_name_length": 3}
{"curie": "UMLS:C5206671", "names": ["Penile Undifferentiated Pleomorphic Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Penile Undifferentiated Pleomorphic Sarcoma", "shortest_name_length": 43}
{"curie": "MONDO:0015269", "names": ["Symmetrical thalamic calcification", "Symmetrical thalamic calcifications", "symmetrical thalamic calcifications", "Bilateral symmetrical thalamic gliosis", "bilateral symmetrical thalamic gliosis", "Symmetrical thalamic calcification (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "symmetrical thalamic calcifications", "shortest_name_length": 34}
{"curie": "MONDO:0020736", "names": ["UHS1", "uncombable hair syndrome", "uncombable hair syndrome 1", "UNCOMBABLE HAIR SYNDROME 1", "pili trianguli Et canaliculi"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uncombable hair syndrome 1", "shortest_name_length": 4}
{"curie": "MONDO:0007953", "names": ["BINDER SYNDROME", "Binder syndrome", "binder syndrome", "Binder's syndrome", "maxillonasal dysplasia", "Maxillonasal dysplasia", "maxillonasal dysostosis", "Maxillonasal dysostosis", "Maxillonasal dysplasia syndrome", "binder type maxillonasal dysplasia", "MAXILLONASAL DYSPLASIA, BINDER TYPE", "MAXILLONASAL dysplasia, BINDER type", "Maxillonasal dysplasia, Binder type", "Maxillonasal dysplasia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Binder syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0030066", "names": ["CGD5", "autosomal recessive chronic granulomatous disease 5", "chronic granulomatous disease 5, autosomal recessive", "granulomatous disease, chronic, autosomal recessive, 5", "GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, 5", "Granulomatous Disease, Chronic, Due to Cybc1 Deficiency", "GRANULOMATOUS DISEASE, CHRONIC, DUE TO CYBC1 DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "granulomatous disease, chronic, autosomal recessive, 5", "shortest_name_length": 4}
{"curie": "MONDO:0009672", "names": ["KWS", "sma3", "SMA3", "Sma 3", "SMA 3", "SMA III", "SMA-III", "SMA type 3", "sma type iii", "SMA type III", "Kugelberg-Welander", "spinal muscular atrophy-3", "Juvenile Muscular Atrophy", "Kugelberg-Welander disease", "kugelberg-welander disease", "Kugelberg-Welander Disease", "MUSCULAR ATROPHY, JUVENILE", "Kugelberg Welander Disease", "muscular atrophy, juvenile", "Muscular Atrophy, Juvenile", "Kugelberg-Welander syndrome", "Kugelberg-Welander Syndrome", "spinal muscular atrophy III", "KUGELBERG-WELANDER SYNDROME", "kugelberg-welander syndrome", "kugelberg welander syndrome", "Spinal Muscular Atrophy III", "Kugelberg Welander Syndrome", "spinal muscular atrophy type 3", "Spinal Muscular Atrophy Type 3", "spinal muscular atrophy, type 3", "Spinal Muscular Atrophy, Type 3", "Type III Spinal Muscular Atrophy", "juvenile spinal muscular atrophy", "Juvenile spinal muscular atrophy", "type III spinal muscular atrophy", "Spinal Muscular Atrophy Type III", "Spinal muscular atrophy type III", "Juvenile Spinal Muscular Atrophy", "Familial spinal muscular atrophy", "Spinal Muscular Atrophy, Type III", "Spinal Muscular Atrophy, Juvenile", "childhood spinal muscular atrophy", "SPINAL MUSCULAR ATROPHY, TYPE III", "Spinal muscular atrophy, juvenile", "WOHLFART-KUGELBERG-WELAN SYNDROME", "spinal muscular atrophy, type III", "Spinal muscular atrophy, familial", "pediatric spinal muscular atrophy", "Spinal muscular atrophy, type III", "spinal muscular atrophy, familial", "Muscular Atrophy, Spinal, Type III", "Spinal Muscular Atrophy of Childhood", "spinal muscular atrophy of childhood", "Kugelberg-Welander disease (disorder)", "Spinal Muscular Atrophies of Childhood", "Kugelberg-Welander disease (diagnosis)", "spinal muscular atrophies of childhood", "Proximal spinal muscular atrophy type 3", "proximal spinal muscular atrophy type 3", "survival motor neuron spinal muscular atrophy", "spinal muscular atrophy, type III, modifier of", "progressive muscular atrophy (Kugelberg-Wellander)", "Hereditary proximal spinal muscular atrophy syndrome", "Spinal Muscular Atrophy, Mild Childhood and Adolescent Form", "spinal muscular atrophy, mild childhood and adolescent form", "SPINAL MUSCULAR ATROPHY, MILD CHILDHOOD AND ADOLESCENT FORM", "atrophy; muscle, spinal, juvenile, type III (Kugelberg-Welander)", "muscle; atrophy, spinal, juvenile, type III (Kugelberg-Welander)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal muscular atrophy, type III", "shortest_name_length": 3}
{"curie": "UMLS:C3873336", "names": ["Primary myoepithelial carcinoma of lung", "Primary myoepithelial carcinoma of lung (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary myoepithelial carcinoma of lung", "shortest_name_length": 39}
{"curie": "MONDO:0008736", "names": ["PBD2B", "Peroxisome Biogenesis Disorder 2B", "peroxisome biogenesis disorder 2B", "PEROXISOME BIOGENESIS DISORDER 2B", "peroxisome biogenesis disorder type 2B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder 2B", "shortest_name_length": 5}
{"curie": "MONDO:0023238", "names": ["Giant mammary hamartoma", "giant mammary hamartoma", "Giant hamartoma of the breast", "giant hamartoma of the breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "giant mammary hamartoma", "shortest_name_length": 23}
{"curie": "MONDO:0003328", "names": ["Fallopian Tube Adenomatoid Tumor", "fallopian tube adenomatoid tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fallopian tube adenomatoid tumor", "shortest_name_length": 32}
{"curie": "MONDO:0043361", "names": ["Cockett syndrome", "Cockett Syndrome", "syndrome, Cockett", "Syndrome, Cockett", "Cockett's syndrome", "May-Thurner syndrome", "May Thurner syndrome", "May Thurner Syndrome", "May-Thurner Syndrome", "Syndrome, May-Thurner", "syndrome, May-Thurner", "Iliocaval compression syndrome", "Iliocaval Compression Syndrome", "syndrome, Iliocaval compression", "Syndrome, Iliocaval Compression", "Iliocaval Compression Syndromes", "Iliac vein compression syndrome", "Iliocaval compression syndromes", "Compression Syndrome, Iliocaval", "Iliac Vein Compression Syndrome", "iliac vein compression syndrome", "compression syndrome, Iliocaval", "Compression Syndromes, Iliocaval", "syndromes, Iliocaval compression", "Syndromes, Iliocaval Compression", "May-Thurner syndrome (diagnosis)", "compression syndromes, Iliocaval", "Iliac vein compression syndrome (disorder)", "disorder of veins compression May-Thurner syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "May-Thurner syndrome", "shortest_name_length": 16}
{"curie": "UMLS:C0686068", "names": ["Cancer metastatic to stomach", "Secondary malignant neoplasm of stomach", "Metastatic malignant neoplasm of stomach", "Metastatic malignant neoplasm to stomach", "Secondary malignant neoplasm of stomach, NOS", "Metastatic Malignant Neoplasm in the Stomach", "Metastatic Malignant Neoplasm to the Stomach", "Metastatic malignant neoplasm to stomach, NOS", "Metastatic malignant neoplasm to stomach (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to stomach", "shortest_name_length": 28}
{"curie": "MONDO:0015037", "names": ["Lissencephaly with cerebellar hypoplasia type D", "lissencephaly with cerebellar hypoplasia type D", "Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D", "Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lissencephaly with cerebellar hypoplasia type D", "shortest_name_length": 47}
{"curie": "MONDO:0007191", "names": ["BD", "Behçet", "Behcet's", "behcet's", "Behcet Disease", "Behçet disease", "behcet disease", "Behcet disease", "Behçet Disease", "BEHCET DISEASE", "Behçet syndrome", "Behçet Syndrome", "behcet diseases", "Bechet syndrome", "Behçet Diseases", "Behcet Syndrome", "behcets disease", "BEHCET SYNDROME", "behcet syndrome", "Behcet syndrome", "Behcet's disease", "Behçet’s disease", "Behçet's disease", "Behet's syndrome", "behcet's disease", "behcets syndrome", "Behcet's Disease", "Behçet's Syndrome", "Behðcet's disease", "Behçet's syndrome", "Behcet's Syndrome", "Behcet's syndrome", "syndrome behcet's", "behcet's syndrome", "silk road disease", "Silk Road Disease", "Behcet's disease, NOS", "Old Silk Route Disease", "Triple-Symptom Complex", "Triple Symptom Complex", "Behcet's syndrome, NOS", "triple symptom complex", "Symptom Complex, Triple", "Triple Symptom Complices", "Morbus Behçet's Syndrome", "Morbus Behçet's syndrome", "BEHCET RECURRENT DISEASE", "OCULOBUCCOGENITAL SYNDROME", "Adamantiades Behcet Disease", "Adamantiades-Behcet disease", "Adamantiades-Behcet Disease", "Adamantiades-Behcet Diseases", "Behcet's syndrome (disorder)", "Behçet-Adamantiades Syndrome", "ADAMANTIADES-BEHCET SYNDROME", "Behçet-Adamantiades syndrome", "Behcet Triple Symptom Complex", "BEHCET TRIPLE SYMPTOM COMPLEX", "Behcet's syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Behcet disease", "shortest_name_length": 2}
{"curie": "MONDO:0030676", "names": ["PKDYS3", "parkinsonism-dystonia 3, childhood-onset", "PARKINSONISM-DYSTONIA 3, CHILDHOOD-ONSET"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parkinsonism-dystonia 3, childhood-onset", "shortest_name_length": 6}
{"curie": "MONDO:0011568", "names": ["DFNA25", "autosomal dominant deafness 25", "DEAFNESS, AUTOSOMAL DOMINANT 25", "Deafness, Autosomal Dominant 25", "deafness, autosomal dominant 25", "deafness, autosomal dominant type 25", "autosomal dominant nonsyndromic deafness 25", "autosomal dominant nonsyndromic hearing loss 25", "autosomal dominant nonsyndromic deafness type 25", "SLC17A8 autosomal dominant nonsyndromic deafness", "autosomal dominant nonsyndromic deafness caused by mutation in SLC17A8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 25", "shortest_name_length": 6}
{"curie": "MONDO:0030024", "names": ["NEDASB", "NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISTIC FEATURES AND/OR STRUCTURAL BRAIN ABNORMALITIES", "neurodevelopmental disorder with or without autistic features and/or structural brain abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with or without autistic features and/or structural brain abnormalities", "shortest_name_length": 6}
{"curie": "UMLS:C0862417", "names": ["Stage III Bladder Urothelial Cancer", "Stage III Bladder Urothelial Carcinoma", "Urothelial carcinoma bladder stage III", "Bladder transitional cell carcinoma stage III", "Stage III Bladder Urothelial Carcinoma AJCC v6", "Stage III Bladder Urothelial Carcinoma AJCC v7", "Stage III Transitional Cell Carcinoma of Bladder", "Transitional cell carcinoma of the bladder stage III", "Stage III Transitional Cell Carcinoma of the Bladder", "Stage III Urinary Bladder Transitional Cell Carcinoma", "Stage III Bladder Urothelial Carcinoma AJCC v6 and v7", "Stage III Transitional Cell Carcinoma of Urinary Bladder", "Stage III Transitional Cell Carcinoma of the Urinary Bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder transitional cell carcinoma stage III", "shortest_name_length": 35}
{"curie": "MONDO:0006515", "names": ["Acute pancreatitis", "Acute Pancreatitis", "PANCREATITIS ACUTE", "Pancreatitis acute", "acute pancreatitis", "Pancreatitis, acute", "Pancreatitis, Acute", "acute; pancreatitis", "Pancreatic Necrosis", "pancreatitis, acute", "pancreatitis; acute", "Pancreatic Necroses", "PANCREATITIS, ACUTE", "Necrosis, Pancreatic", "Acute Pancreatitides", "Pancreatitides, Acute", "AP - Acute pancreatitis", "NECROTIZING PANCREATITIS", "PANCREATITIS NECROTIZING", "necrotising pancreatitis", "Necrotizing pancreatitis", "Pancreatitis necrotizing", "Pancreatitis Necrotizing", "Necrotising pancreatitis", "PANCREATITIS NECROTISING", "Pancreatitis necrotising", "necrotizing pancreatitis", "Pancreatitis Necrotising", "Pancreatitis Necrotisings", "Pancreatitis Necrotizings", "Acute pancreatitis (disorder)", "Acute pancreatic inflammation", "Acute necrotizing pancreatitis", "acute necrotising pancreatitis", "acute pancreatitis (diagnosis)", "Acute necrotising pancreatitis", "Acute Necrotizing Pancreatitis", "acute pancreatitis necrotizing", "acute necrotizing pancreatitis", "Pancreatitis, Acute Necrotizing", "Necrotizing Pancreatitis, Acute", "Acute pancreatitis, unspecified", "acute pancreatitis (disorder) [ambiguous]", "Acute necrotizing pancreatitis (disorder)", "Acute necrotizing pancreatitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute pancreatitis", "shortest_name_length": 18}
{"curie": "MONDO:0007290", "names": ["CTM", "CAM", "CTRCT5", "zonular cataract", "Zonular cataract", "Lamellar cataract", "Cataract, zonular", "zonular; cataract", "cataract; zonular", "lamellar cataract", "Cataract, lamellar", "CATARACT, LAMELLAR", "cataract, lamellar", "Perinuclear cataract", "cataract, Marner type", "Cataract, Marner Type", "CATARACT, MARNER TYPE", "HSF4 cataract (disease)", "cataract 5 multiple types", "cataract 5, multiple types", "CATARACT 5, MULTIPLE TYPES", "cataract (disease) caused by mutation in HSF4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 5 multiple types", "shortest_name_length": 3}
{"curie": "MONDO:0013140", "names": ["CANDF4", "candidiasis, familial, 4", "CANDIDIASIS, FAMILIAL, 4", "Candidiasis, Familial, Type 4", "candidiasis, familial, type 4", "Familial chronic mucocutaneous candidosis", "Familial chronic mucocutaneous candidiasis", "CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS", "candidiasis, familial chronic mucocutaneous", "Candidiasis, Familial Chronic Mucocutaneous", "candidiasis, familial, 4, autosomal recessive", "FCMC - Familial chronic mucocutaneous candidosis", "CLEC7A familial chronic mucocutaneous candidiasis", "FCMC - Familial chronic mucocutaneous candidiasis", "Familial chronic mucocutaneous candidiasis (disorder)", "familial chronic mucocutaneous candidiasis caused by mutation in CLEC7A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "candidiasis, familial, 4", "shortest_name_length": 6}
{"curie": "MONDO:0012465", "names": ["GPID", "GPIBD1", "PIGM-CDG", "GPI deficiency", "GLYCOSYLPHOSPHATIDYLINOSITOL DEFICIENCY", "glycosylphosphatidylinositol deficiency", "Glycosylphosphatidylinositol deficiency", "glycosylphosphatidylinositol biosynthesis defect 1", "GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 1", "PORTAL HYPERTENSION WITH SEIZURES AND/OR MACROCEPHALY", "congenital disorder of glycosylation due to PIGM deficiency", "Congenital disorder of glycosylation due to PIGM deficiency", "Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency", "hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency", "Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency", "shortest_name_length": 4}
{"curie": "UMLS:C0266487", "names": ["État marbré", "Etat marbre", "Etat Marbre", "Status Marmoratus", "status marmoratus", "Status marmoratus", "status; marmoratus", "marmoratus; status", "Status marmoratus (disorder)", "status marmoratus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Etat Marbre", "shortest_name_length": 11}
{"curie": "UMLS:C3898473", "names": ["Malignant Biliary Obstruction", "malignant biliary obstruction", "Malignant biliary obstruction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant biliary obstruction", "shortest_name_length": 29}
{"curie": "UMLS:C0677956", "names": ["Stage II Non-Hodgkin Lymphoma", "Stage II Non-Hodgkin's Lymphoma", "Non-Hodgkin's Lymphoma Stage II", "Non-Hodgkin's lymphoma stage II", "Non-Hodgkin's lymphoma NOS stage II", "Ann Arbor Stage II Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Non-Hodgkin Lymphoma", "shortest_name_length": 29}
{"curie": "UMLS:C0685928", "names": ["parotitis suppurative", "Suppurative Parotitis", "Suppurative parotitis", "suppurative parotitis", "PAROTITIS SUPPURATIVE", "Suppurative parotitis (disorder)", "suppurative parotitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Suppurative parotitis", "shortest_name_length": 21}
{"curie": "UMLS:C0751173", "names": ["Infantile Glycogen Storage Disease Type II", "Glycogen Storage Disease Type II, Infantile"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Glycogen Storage Disease Type II, Infantile", "shortest_name_length": 42}
{"curie": "UMLS:C0751915", "names": ["Atypical Pelizaeus-Merzbacher Disease", "Atypical Pelizaeus Merzbacher Disease", "Pelizaeus Merzbacher Disease, Atypical", "Pelizaeus-Merzbacher Disease, Atypical", "PELIZAEUS-MERZBACHER DISEASE, ATYPICAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pelizaeus-Merzbacher Disease, Atypical", "shortest_name_length": 37}
{"curie": "UMLS:C3897729", "names": ["Refractory Hodgkin Lymphoma", "Refractory Childhood Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Childhood Hodgkin Lymphoma", "shortest_name_length": 27}
{"curie": "UMLS:C4743578", "names": ["Unresectable Malignant Mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Malignant Mesothelioma", "shortest_name_length": 35}
{"curie": "MONDO:0018923", "names": ["VCFS", "22q11DS", "catch 22", "Takao syndrome", "monosomy 22q11", "DiGeorge syndrome", "DiGeorge sequence", "Sedlackova syndrome", "Shprintzen syndrome", "microdeletion 22q11.2", "velocardiofacial syndrome", "22q11.2 deletion syndrome", "Cayler cardiofacial syndrome", "conotruncal anomaly face syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "22q11.2 deletion syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0006567", "names": ["kernicterus - due to isoimm.", "Kernicterus due to isoimmunisation", "kernicterus due to isoimmunization", "Kernicterus due to isoimmunization", "Kernicterus due to Isoimmunization", "isoimmunized kernicterus of newborn", "Kernicterus related to Isoimmunization", "kernicterus related to isoimmunization", "Kernicterus Related to Isoimmunization", "isoimmunization; fetus, with kernicterus", "kernicterus; newborn, due to isoimmunization", "kernicterus; jaundice, due to isoimmunization", "jaundice; kernicterus, due to isoimmunization", "Kernicterus due to isoimmunization (disorder)", "isoimmunized kernicterus of newborn (diagnosis)", "Kernicterus of fetus or newborn due to isoimmunization", "Kernicterus due to isoimmunization of fetus or newborn", "kernicterus due to isoimmunization of fetus or newborn", "Kernicterus due to isoimmunisation of foetus or newborn"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kernicterus due to isoimmunization", "shortest_name_length": 28}
{"curie": "UMLS:C1334234", "names": ["Intra-Abdominal Lymphangioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intra-Abdominal Lymphangioma", "shortest_name_length": 28}
{"curie": "MONDO:0000448", "names": ["chemodectoma", "Paraganglioma", "paraganglioma", "paragangliomas", "Paragangliomas", "Paragangliomata", "Paragangliomatas", "Paraganglioma NOS", "glomus body tumor", "Paraganglion Tumor", "Paraganglioma, NOS", "paraganglion tumor", "Carotid body tumors", "Paraganglionic Tumor", "Paraganglionic tumor", "Carotid body tumours", "paraganglia neoplasm", "Paraganglion Neoplasm", "Tumor of Paraganglion", "paraganglion neoplasm", "tumor of paraganglion", "Paraganglion neoplasm", "Paraganglionic neoplasm", "Paraganglionic Neoplasm", "neoplasm of paraganglia", "Neoplasm of Paraganglion", "Neoplasm of paraganglion", "Paraganglioma (disorder)", "neoplasm of paraganglion", "Paraganglion neoplasm NOS", "tumor of the paraganglion", "Tumor of the Paraganglion", "gangliocytic paraganglioma", "Gangliocytic paraganglioma", "Gangliocytic Paraganglioma", "paraganglioma gangliocytic", "paragangliomas (diagnosis)", "Gangliocytic Paragangliomas", "Paraganglioma, Gangliocytic", "neoplasm of the paraganglion", "Neoplasm of the Paraganglion", "paragangliomas (chemodectoma)", "Neoplasm of paraganglion (disorder)", "neoplasm of paraganglia (diagnosis)", "Gangliocytic paraganglioma (disorder)", "gangliocytic paraganglioma (diagnosis)", "Paraganglioma (morphologic abnormality)", "gangliocytic; paraganglioma, unspecified site", "paraganglioma; gangliocytic, unspecified site", "Gangliocytic paraganglioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paraganglioma", "shortest_name_length": 12}
{"curie": "UMLS:C4688319", "names": ["Refractory Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Melanoma", "shortest_name_length": 19}
{"curie": "UMLS:C1866091", "names": ["Left-Right Axis Malformations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Left-Right Axis Malformations", "shortest_name_length": 29}
{"curie": "MONDO:0016186", "names": ["qualitative or quantitative defects of myofibrillar proteins"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of myofibrillar proteins", "shortest_name_length": 60}
{"curie": "UMLS:C3273095", "names": ["Gallbladder ICPN with High Grade Intraepithelial Neoplasia", "Gallbladder Intracholecystic Papillary Neoplasm, High Grade", "Gallbladder Intracholecystic Papillary Neoplasm, High-Grade", "Intracystic Papillary Neoplasm with High Grade Intraepithelial Neoplasia", "Gallbladder Papillary Neoplasm with High Grade Intraepithelial Neoplasia", "Gallbladder Intracholecystic Papillary Neoplasm with High Grade Intraepithelial Neoplasia", "Gallbladder Intracystic/Intaductal Papillary Neoplasm with High Grade Intraepithelial Neoplasia", "Gallbladder Intracholecystic Papillary (Tubular) Neoplasm with High Grade Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gallbladder Intracholecystic Papillary Neoplasm, High Grade", "shortest_name_length": 58}
{"curie": "MONDO:8000018", "names": ["BRV", "BPPV", "familial vestibulopathy", "Familial Vestibulopathy", "benign recurrent vertigo", "Vestibulopathy, Familial", "vestibulopathy, familial", "Benign recurrent vertigo", "VESTIBULOPATHY, FAMILIAL", "Benign Recurrent Vertigo", "Benign positional vertigo", "Vertigo;benign positional", "Benign Recurrent Vertigos", "vertigo, benign recurrent", "vertigo benign positional", "VERTIGO BENIGN POSITIONAL", "Familial Vestibulopathies", "Vertigo, Benign Recurrent", "benign positional vertigo", "positional benign vertigo", "Recurrent Vertigo, Benign", "VERTIGO, BENIGN RECURRENT", "positional vertigo benign", "BENIGN POSITIONAL VERTIGO", "Vestibulopathies, Familial", "Recurrent Vertigos, Benign", "Familial Benign Recurrent Vertigo", "familial benign recurrent vertigo", "Benign paroxysmal postural vertigo", "Benign recurrent vertigo (disorder)", "NYSTAGMUS, POSITIONAL, LABYRINTHINE", "Benign Paroxysmal Positional Vertigo", "benign recurrent vertigo (diagnosis)", "benign paroxysmal positional vertigo", "Benign paroxysmal positional vertigo", "VERTIGO, BENIGN PAROXYSMAL POSITIONAL", "vertigo, benign paroxysmal positional", "Vertigo, Benign Paroxysmal Positional", "VERTIGO, PAROXYSMAL POSITIONAL, BENIGN", "benign paroxysmal positional nystagmus", "Benign paroxysmal positional nystagmus", "NYSTAGMUS, PAROXYSMAL POSITIONAL, BENIGN", "BPPV - Benign paroxysmal positional vertigo", "BPPV (benign paroxysmal positional vertigo)", "Benign paroxysmal positional vertigo (disorder)", "benign paroxysmal positional vertigo (diagnosis)", "benign paroxysmal positional nystagmus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign paroxysmal positional vertigo", "shortest_name_length": 3}
{"curie": "UMLS:C0153775", "names": ["Stage III Mixed Cellularity Hodgkin Lymphoma", "Mixed Cellularity Hodgkin's Disease Stage III", "Hodgkin's disease mixed cellularity stage III", "Stage III Mixed Cellularity Hodgkin's Disease", "Mixed Cellularity Hodgkin's Lymphoma Stage III", "Stage III Mixed Cellularity Hodgkin's Lymphoma", "Stage III Mixed Cellularity Classical Hodgkin Lymphoma", "Ann Arbor Stage III Mixed Cellularity Classic Hodgkin Lymphoma", "Ann Arbor Stage III Mixed Cellularity Classical Hodgkin Lymphoma", "Hodgkin's disease, mixed cellularity, lymph nodes of multiple sites", "Hodgkin's disease, mixed cellularity, involving lymph nodes of multiple sites"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's disease mixed cellularity stage III", "shortest_name_length": 44}
{"curie": "UMLS:C1266039", "names": ["Clear cell borderline tumor", "Clear cell borderline tumour", "Clear cell tumor, atypical proliferative", "Clear cell tumour, atypical proliferative", "Borderline Ovarian Clear Cell Adenofibroma", "Clear cell adenofibroma of borderline malignancy", "Clear cell cystadenofibroma of borderline malignancy", "Clear cell adenofibroma of borderline malignancy (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clear cell adenofibroma of borderline malignancy", "shortest_name_length": 27}
{"curie": "UMLS:C1336445", "names": ["IV", "Stage IV Uveal Melanoma", "Stage IV Melanoma of Uvea", "Stage IV Melanoma of the Uvea", "Stage IV Uveal Melanoma AJCC v7", "Stage IV Uveal Malignant Melanoma", "Stage IV Malignant Melanoma of Uvea", "Stage IV Malignant Melanoma of the Uvea"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Uveal Melanoma AJCC v7", "shortest_name_length": 2}
{"curie": "UMLS:C3897744", "names": ["Recurrent Pleomorphic Xanthoastrocytoma", "Recurrent Childhood Pleomorphic Xanthoastrocytoma", "recurrent childhood pleomorphic xanthoastrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Pleomorphic Xanthoastrocytoma", "shortest_name_length": 39}
{"curie": "MONDO:0005939", "names": ["Reovirus Infection", "Reovirus infection", "Reoviridae disease", "Reovirus Infections", "Infection, Reovirus", "Reovirus infections", "infection, Reovirus", "Reoviridae Infection", "Infections, Reovirus", "infections, Reovirus", "Reoviridae infection", "Infection, Reoviridae", "infection, Reoviridae", "Reoviridae Infections", "Infections, Reoviridae", "infections, Reoviridae", "Reovirus infection, NOS", "Disease due to Reovirus", "DISEASES DUE TO REOVIRUS", "Disease due to Reoviridae", "Disease caused by Reovirus", "DISEASES DUE TO REOVIRIDAE", "Disease caused by Reoviridae", "Disease due to Reovirus, NOS", "Disease due to Orthoreovirus", "Reoviridae infectious disease", "Disease caused by Orthoreovirus", "Disease caused by Reoviridae (disorder)", "Disease caused by Orthoreovirus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reoviridae infectious disease", "shortest_name_length": 18}
{"curie": "MONDO:0007994", "names": ["Cloverleaf skull micromelia thoracic dysplasia", "Micromelic bone dysplasia with cloverleaf skull", "MICROMELIC BONE DYSPLASIA WITH CLOVERLEAF SKULL", "micromelic bone dysplasia with cloverleaf skull"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "micromelic bone dysplasia with cloverleaf skull", "shortest_name_length": 46}
{"curie": "UMLS:C4683651", "names": ["B-Cell Non-Hodgkin Lymphoma by Ann Arbor Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-Cell Non-Hodgkin Lymphoma by Ann Arbor Stage", "shortest_name_length": 46}
{"curie": "UMLS:C5206601", "names": ["Paratesticular Cellular Angiofibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paratesticular Cellular Angiofibroma", "shortest_name_length": 36}
{"curie": "MONDO:0022623", "names": ["CDK4 linked melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CDK4 linked melanoma", "shortest_name_length": 20}
{"curie": "MONDO:0015757", "names": ["lymphoid hemopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphoid hemopathy", "shortest_name_length": 18}
{"curie": "MONDO:0026732", "names": ["CHNG9", "congenital nongoitrous hypothyroidism 9", "hypothyroidism, congenital, nongoitrous, 9", "HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 9", "hypothyroidism, congenital, nongoitrous, 9, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypothyroidism, congenital, nongoitrous, 9", "shortest_name_length": 5}
{"curie": "MONDO:0004802", "names": ["PIE", "andrews syndrome", "Andrews syndrome", "Eosinophilic asthma", "pulmonary eosinophilia", "PULMONARY EOSINOPHILIA", "Eosinophilic pneumonia", "Pulmonary Eosinophilia", "Pulmonary eosinophilia", "pulmonary; eosinophilia", "eosinophilia; pulmonary", "Pulmonary Eosinophilias", "Eosinophilia, Pulmonary", "Eosinophilias, Pulmonary", "eosinophilic pneumonitis", "PNEUMONITIS, EOSINOPHILIC", "pneumonitis; eosinophilic", "eosinophilic; pneumonitis", "eosinophilic pulmonary reactions", "Pulmonary eosinophilia (disorder)", "Pulmonary eosinophilic infiltrate", "PULMONARY INFILTRATION EOSINOPHILIA", "Eosinophilic pulmonary infiltration", "Pulmonary infiltration eosinophilic", "Pulmonary eosinophilic infiltration", "Pulmonary infiltrates with eosinophilia", "eosinophilic pulmonary reactions (diagnosis)", "PIE - Pulmonary infiltrates with eosinophilia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary eosinophilia", "shortest_name_length": 3}
{"curie": "MONDO:0019973", "names": ["Persistent placoid maculopathy", "persistent placoid maculopathy", "Persistent placoid maculopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "persistent placoid maculopathy", "shortest_name_length": 30}
{"curie": "UMLS:C4520739", "names": ["stage I salivary gland cancer", "Stage I Salivary Gland Cancer", "Stage I Salivary Gland Carcinoma", "Stage I Major Salivary Gland Cancer", "Stage I Major Salivary Gland Carcinoma", "Stage I Carcinoma of Major Salivary Gland", "Stage I Major Salivary Gland Cancer AJCC v7", "Stage I Carcinoma of the Major Salivary Gland", "Stage I Major Salivary Gland Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Major Salivary Gland Cancer AJCC v7", "shortest_name_length": 29}
{"curie": "MONDO:0024183", "names": ["wet beriberi"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "wet beriberi", "shortest_name_length": 12}
{"curie": "MONDO:0000596", "names": ["Paraphilia", "paraphilia", "paraphilias", "Paraphilias", "paraepithymia", "Sex deviation", "Sex Deviation", "parasexuality", "Paraphilia NOS", "deviation, Sex", "Sex Deviations", "Deviation, Sex", "Paraphilia, NOS", "Deviations, Sex", "Sexual deviation", "sexual deviation", "Sexual Deviation", "deviation; sexual", "sexual deviations", "sexual perversion", "sexual; deviation", "Sexual perversion", "Sexual Deviations", "Sexual aberration", "aberrations sexual", "perversion; sexual", "sexual; perversion", "paraphilia disorder", "Deviations (Sexual)", "Paraphilic Disorder", "paraphilic disorder", "Paraphilic Disorders", "Disorder, Paraphilic", "disorders paraphilia", "disorder, Paraphilic", "Perversions (Sexual)", "Sexual deviation NOS", "Sexual deviation, NOS", "Paraphilia (disorder)", "Disorders, Paraphilic", "disorders, Paraphilic", "Sexual aberration, NOS", "Sexual perversion, NOS", "paraphilia (diagnosis)", "Unspecified sexual deviation", "Disorder of sexual preference", "disorder of sexual preference", "Sexual deviations or disorders", "Disorders of sexual preference", "paraphilia disorder (diagnosis)", "Sexual deviation disease or syndrome", "disorder of sexual preference (diagnosis)", "Disorder of sexual preference, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paraphilic disorder", "shortest_name_length": 10}
{"curie": "MONDO:0014200", "names": ["PASNA", "Conn adenoma", "aldosteronoma", "aldosterone-secreting adenoma", "primary aldosteronism due to Conn adenoma", "APA with seizures and neurological abnormalities", "Conn adenoma with seizures and neurological abnormalities", "primary aldosteronism, seizures, and neurologic abnormalities", "Primary Aldosteronism, Seizures, and Neurologic Abnormalities", "PRIMARY ALDOSTERONISM, SEIZURES, AND NEUROLOGIC ABNORMALITIES", "aldosterone-secreting adenoma with seizures and neurological abnormalities", "aldosterone-producing adenoma with seizures and neurological abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aldosterone-producing adenoma with seizures and neurological abnormalities", "shortest_name_length": 5}
{"curie": "MONDO:0010905", "names": ["Crd1", "CRD1", "CORD1", "CONE-ROD DYSTROPHY 1", "cone-rod dystrophy 1", "Cone-Rod Dystrophy 1", "cone-rod dystrophy type 1", "cone-rod retinal dystrophy-1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cone-rod dystrophy 1", "shortest_name_length": 4}
{"curie": "UMLS:C4526967", "names": ["Stage IB Gastric and Omental GIST AJCC v8", "Stage IB Gastric and Omental Gastrointestinal Stromal Tumor AJCC v8", "Stage IB Gastric (Stomach) and Omental Gastrointestinal Stromal Tumor (GIST)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Gastric and Omental Gastrointestinal Stromal Tumor AJCC v8", "shortest_name_length": 41}
{"curie": "MONDO:0018968", "names": ["Iniencephaly", "iniencephaly", "INIENCEPHALY", "iniencephalus", "Iniencephalus", "Iniencephalies", "Iniencephaly (disorder)", "iniencephaly (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "iniencephaly", "shortest_name_length": 12}
{"curie": "MONDO:0018567", "names": ["CMT2 due to TFG mutation", "autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation", "shortest_name_length": 24}
{"curie": "UMLS:C4683545", "names": ["Adrenal Gland Pheochromocytoma and Sympathetic Paraganglioma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adrenal Gland Pheochromocytoma and Sympathetic Paraganglioma by AJCC v8 Stage", "shortest_name_length": 77}
{"curie": "UMLS:C0428908", "names": ["SINUS NODE DISEASE", "Sinus Node Disease", "Sinus Node Diseases", "Sinus node dysfunction", "sinus node dysfunction", "Sinus Node Dysfunction", "Dysfunction, Sinus Node", "Dysfunctions, Sinus Node", "Sinoatrial node dysfunction", "sinoatrial node dysfunction", "Coronary sinus rhythm disorder", "Rhythm disorder, coronary sinus", "Sinus node dysfunction (disorder)", "Sinus Node Dysfunction (disorder)", "sinoatrial node dysfunction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinus Node Dysfunction (disorder)", "shortest_name_length": 18}
{"curie": "MONDO:0008831", "names": ["ATD1", "SRTD1", "Jeune syndrome", "asphyxiating thoracic dystrophy 1", "ASPHYXIATING THORACIC DYSTROPHY 1", "Asphyxiating Thoracic Dystrophy 1", "thoracic-pelvic-phalangeal dystrophy", "asphyxiating thoracic dystrophy type 1", "SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY", "short-rib thoracic dysplasia 1 with or without polydactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "asphyxiating thoracic dystrophy 1", "shortest_name_length": 4}
{"curie": "UMLS:C3275111", "names": ["Mild Cardiac Valve Regurgitation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mild Cardiac Valve Regurgitation", "shortest_name_length": 32}
{"curie": "UMLS:C0346055", "names": ["Skin Neural Tumor", "Skin Neural Neoplasm", "Neural Tumor of Skin", "Neural Neoplasm of Skin", "Neural Tumor of the Skin", "Cutaneous Neural Neoplasm", "Skin mass of neural origin", "Skin Tumor of Neural Origin", "Neural Neoplasm of the Skin", "Skin tumor of neural origin", "Skin tumour of neural origin", "Skin Neoplasm of Neural Origin", "Skin tumor of neural origin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin tumor of neural origin", "shortest_name_length": 17}
{"curie": "UMLS:C0275583", "names": ["Pulmonary Nocardiosis", "PULMONARY NOCARDIOSIS", "Pulmonary nocardiosis", "nocardiosis pulmonary", "Pulmonary Nocardioses", "Nocardiosis, Pulmonary", "Nocardioses, Pulmonary", "nocardiosis; lung (etiology)", "lung; nocardiosis (etiology)", "Pulmonary nocardiosis (disorder)", "Pulmonary nocardiosis (diagnosis)", "nocardiosis; pulmonary (etiology)", "lung; nocardiosis (manifestation)", "pulmonary; nocardiosis (etiology)", "nocardiosis; lung (manifestation)", "nocardiosis; pulmonary (manifestation)", "pulmonary; nocardiosis (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pulmonary Nocardiosis", "shortest_name_length": 21}
{"curie": "MONDO:0027749", "names": ["serpinopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "serpinopathy", "shortest_name_length": 12}
{"curie": "MONDO:0018963", "names": ["hemoglobin m disease", "Hereditary methemoglobinemia", "Congenital methemoglobinemia", "hereditary methemoglobinemia", "congenital methemoglobinemia", "Congenital Methemoglobinemia", "congenital; methemoglobinemia", "methemoglobinemia; congenital", "Methemoglobinemia, congenital", "Congenital methaemoglobinaemia", "Autosomal recessive methemoglobinemia", "autosomal recessive methemoglobinemia", "Congenital methemoglobinemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary methemoglobinemia", "shortest_name_length": 20}
{"curie": "UMLS:C3898153", "names": ["Sclerosing Funisitis", "Necrotizing Funisitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Necrotizing Funisitis", "shortest_name_length": 20}
{"curie": "MONDO:0015146", "names": ["ILS", "lissencephaly type 1", "lissencephaly classic", "classic lissencephaly", "lissencephaly sequence isolated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "classic lissencephaly", "shortest_name_length": 3}
{"curie": "MONDO:0014919", "names": ["SSPCS", "SESSILE SERRATED POLYPOSIS CANCER SYNDROME", "sessile serrated polyposis cancer syndrome", "sessile serrated polyposis cancer syndrome; SSPCS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sessile serrated polyposis cancer syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0013592", "names": ["NDNC9", "Nail deformed", "Claw deformed", "nail dysplasia", "Nail dystrophy", "NAIL DYSPLASIA", "nail dystrophy", "NAIL DYSTROPHY", "dystrophy; nail", "Dystrophic nail", "onychodystrophy", "Dystrophic claw", "dystrophic nail", "ONYCHODYSTROPHY", "Onychodystrophy", "nail; dystrophy", "dystrophic nails", "Dystrophic nails", "Nail Dystrophies", "Dystrophia unguium", "Poor nail formation", "nails onychodystrophy", "nail dystrophy was noted", "onychodystrophy was noted", "nail dystrophy (diagnosis)", "Dystrophia unguium (disorder)", "anonychia-onycholysis, isolated", "ANONYCHIA-ONYCHOLYSIS, ISOLATED", "nail dystrophy (physical finding)", "onychodystrophy (physical finding)", "nonsyndromic congenital nail disorder 9", "NAIL DISORDER, NONSYNDROMIC CONGENITAL, 9", "nail disorder, nonsyndromic congenital, 9", "dermatology non-infectious nails dystrophy", "nonsyndromic congenital nail disorder type 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nonsyndromic congenital nail disorder 9", "shortest_name_length": 5}
{"curie": "MONDO:0022220", "names": ["parinaud syndrome", "Parinaud syndrome", "Parinaud Syndrome", "parinauds syndrome", "syndrome, Parinaud", "Parinauds Syndrome", "Syndrome, Parinaud", "Parinauds syndrome", "Parinaud's Syndrome", "parinaud's syndrome", "Parinaud's syndrome", "Syndrome, Parinaud's", "syndrome, Parinaud's", "syndrome; parinaud's", "parinaud's; syndrome", "Dorsal Midbrain Syndrome", "Dorsal midbrain syndrome", "dorsal midbrain syndrome", "Parinaud's ophthalmoplegia", "parinaud's; ophthalmoplegia", "ophthalmoplegia; parinaud's", "Vertical gaze palsy - Parinaud", "vertical gaze palsy - Parinaud", "paralysis of vertical movement", "Paralysis of vertical movement", "Parinaud's syndrome (disorder)", "Parinaud's syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parinaud syndrome", "shortest_name_length": 17}
{"curie": "MONDO:0001876", "names": ["Renal atherosclerosis", "renal atherosclerosis", "Renal artery atheroma", "renal artery atheroma", "atheroma of renal artery", "Atherosclerosis renal artery", "renal artery atherosclerosis", "RENAL ARTERY ATHEROSCLEROSIS", "Renal artery atherosclerosis", "Atherosclerosis of renal artery", "atherosclerosis of renal artery", "atheroma of renal artery (diagnosis)", "Atherosclerosis of renal artery (disorder)", "atherosclerosis of renal artery (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal artery atheroma", "shortest_name_length": 21}
{"curie": "MONDO:0004616", "names": ["herpetic felon", "Herpetic felon", "whitlow herpetic", "herpetic whitlow", "Herpetic Whitlow", "Herpetic whitlow", "HERPETIC WHITLOW", "Herpes simplex whitlow", "herpetic felon (diagnosis)", "Herpetic whitlow (disorder)", "Simplexvirus paronychia (disease)", "Simplexvirus caused paronychia (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "herpetic whitlow", "shortest_name_length": 14}
{"curie": "MONDO:0002976", "names": ["stomach diverticulosis", "Gastric Diverticulosis", "Stomach Diverticulosis", "Diverticulosis, Gastric", "Diverticulosis, Stomach"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stomach diverticulosis", "shortest_name_length": 22}
{"curie": "UMLS:C4745067", "names": ["Locally Advanced Unresectable Basal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Unresectable Basal Cell Carcinoma", "shortest_name_length": 50}
{"curie": "UMLS:C4682758", "names": ["Post-Mastectomy Pain Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post-Mastectomy Pain Syndrome", "shortest_name_length": 29}
{"curie": "MONDO:0009961", "names": ["Renal and Mullerian Duct Hypoplasia", "renal and mullerian duct hypoplasia", "RENAL AND MULLERIAN DUCT HYPOPLASIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal and mullerian duct hypoplasia", "shortest_name_length": 35}
{"curie": "UMLS:C0234305", "names": ["Secondary salt taste disorder", "Taste Disorder, Secondary, Salt", "Taste disorder, secondary, salt", "Secondary salt taste disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Taste Disorder, Secondary, Salt", "shortest_name_length": 29}
{"curie": "UMLS:C5446515", "names": ["Conjunctival Non-Hodgkin Lymphoma", "Primary Conjunctival Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conjunctival Non-Hodgkin Lymphoma", "shortest_name_length": 33}
{"curie": "MONDO:0014792", "names": ["PDB6", "PAGET DISEASE OF BONE 6", "Paget disease of bone-6", "Paget disease of bone 6", "Paget's disease of bone 6", "Paget disease of bone type 6", "Paget disease of bone 6; PDB6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paget disease of bone 6", "shortest_name_length": 4}
{"curie": "MONDO:0054615", "names": ["SPGF18", "spermatogenic failure 18", "SPERMATOGENIC FAILURE 18"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 18", "shortest_name_length": 6}
{"curie": "UMLS:C0729586", "names": ["Infective otitis media", "otitis media infective", "Infective otitis media (disorder)", "Infective otitis media (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infective otitis media", "shortest_name_length": 22}
{"curie": "UMLS:C1710412", "names": ["Thyroid Gland Follicular Adenoma with Papillary Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Follicular Adenoma with Papillary Hyperplasia", "shortest_name_length": 59}
{"curie": "UMLS:C5420072", "names": ["Primary Sinonasal Meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Sinonasal Meningioma", "shortest_name_length": 28}
{"curie": "MONDO:0100038", "names": ["complex neurodevelopmental disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complex neurodevelopmental disorder", "shortest_name_length": 35}
{"curie": "UMLS:C2987254", "names": ["Well Differentiated Esophageal Squamous Cell Cancer", "Esophageal Well Differentiated Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Well Differentiated Squamous Cell Carcinoma", "shortest_name_length": 51}
{"curie": "MONDO:0008125", "names": ["NDNC5", "Hereditary distal onycholysis", "ONYCHOLYSIS, HEREDITARY DISTAL", "onycholysis, hereditary distal", "onycholysis, partial, with scleronychia", "Onycholysis, Partial, with Scleronychia", "nonsyndromic congenital nail disorder 5", "ONYCHOLYSIS, PARTIAL, WITH SCLERONYCHIA", "Hereditary distal onycholysis (disorder)", "NAIL DISORDER, NONSYNDROMIC CONGENITAL, 5", "nail disorder, nonsyndromic congenital, 5", "nonsyndromic congenital nail disorder type 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nonsyndromic congenital nail disorder 5", "shortest_name_length": 5}
{"curie": "UMLS:C0279951", "names": ["low-grade, stage I adult NHL", "NHL, low grade, stage I adult", "adult NHL, stage I, low grade", "Stage I Low Grade Adult Non-Hodgkin's Lymphoma", "lymphoma, low grade, stage I adult non-Hodgkin's", "non-Hodgkin's lymphoma, low grade, stage I adult", "adult non-Hodgkin's lymphoma, low grade, stage I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Low Grade Adult Non-Hodgkin's Lymphoma", "shortest_name_length": 28}
{"curie": "MONDO:0011869", "names": ["EBSS", "epidermolysis bullosa simplex superficialis", "EPIDERMOLYSIS BULLOSA SIMPLEX SUPERFICIALIS", "Epidermolysis Bullosa Simplex Superficialis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolysis bullosa simplex superficialis", "shortest_name_length": 4}
{"curie": "MONDO:0010837", "names": ["HYPERPARATHYROID PRIMARY", "hyperparathyroidism primary", "Primary Hyperparathyroidism", "primary hyperparathyroidism", "Primary hyperparathyroidism", "HYPERPARATHYROIDISM PRIMARY", "Hyperparathyroidism primary", "Hyperparathyroidism, primary", "Hyperparathyroidism, Primary", "hyperparathyroidism; primary", "familial hyperparathyroidism", "Familial hyperparathyroidism", "hyperparathyroidism familial", "Primary Hyperparathyroidisms", "primary; hyperparathyroidism", "HYPERPARATHYROIDISM, PRIMARY", "Hyperparathyroidisms, Primary", "Hyperparathyroidism, familial", "hyperparathyroidism, familial", "Familial primary hyperparathyroidism", "familial primary hyperparathyroidism", "primary hyperparathyroidism (disease)", "Primary hyperparathyroidism (disorder)", "Primary hyperparathyroidism (diagnosis)", "familial hyperparathyroidism (diagnosis)", "Familial primary hyperparathyroidism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary hyperparathyroidism", "shortest_name_length": 24}
{"curie": "MONDO:0010565", "names": ["CBP", "Red-weak", "Protanopia", "protanopia", "PROTANOMALY", "protanomaly", "Protanomaly", "protan defect", "Protan defect", "Protan Defect", "red color defect", "red colorblindness", "RED COLORBLINDNESS", "Protan defect (red)", "Red Color Blindness", "red color blindness", "RED COLOR BLINDNESS", "Color Blindness, Red", "colorblindness, protan", "Protan defect (disorder)", "protan defect (diagnosis)", "partial achromatopsia, protan type", "red color defect (physical finding)", "COLORBLINDNESS, PARTIAL, PROTAN SERIES", "colorblindness, partial, protan series", "Colorblindness, partial, protan series"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "red color blindness", "shortest_name_length": 3}
{"curie": "UMLS:C0153687", "names": ["skin metastasis", "metastasis skin", "Skin Metastasis", "Skin Metastases", "Skin metastases", "skin metastases", "Skin secondaries", "Dermal metastasis", "Metastases to skin", "Metastases to Skin", "Metastasis to skin", "Metastasis to Skin", "cutaneous metastasis", "Cutaneous metastasis", "Skin cancer metastatic", "metastasis to the skin", "metastatic skin cancer", "Metastases to skin, NOS", "Secondary cancer of skin", "Cancer metastatic to skin", "metastatic cancer to skin", "skin, metastatic cancer to", "cancer, metastatic to skin", "Metastatic Tumor to the Skin", "Malignant infiltration of skin", "Metastatic Neoplasm to the Skin", "secondary malignant neoplasm skin", "Secondary malignant neoplasm of skin", "secondary malignant neoplasm of skin", "Metastatic malignant neoplasm to skin", "Metastatic malignant neoplasm of skin", "metastasis of malignant neoplasm to skin", "Metastatic Malignant Neoplasm in the Skin", "Metastatic Malignant Neoplasm to the Skin", "Secondary malignant neoplasm of skin, NOS", "Metastatic malignant neoplasm to skin, NOS", "Metastatic malignant neoplasm to skin (disorder)", "secondary malignant neoplasm of skin (diagnosis)", "metastasis of malignant neoplasm to skin (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary malignant neoplasm of skin", "shortest_name_length": 15}
{"curie": "MONDO:0002614", "names": ["Osteitis", "osteitis", "Osteitis NOS", "Osteitis, NOS", "Bone Inflammation", "Bone inflammation", "bone inflammation", "bones inflammation", "Inflammation, Bone", "bone inflammation of", "osteitis (diagnosis)", "inflammation of bone", "Inflammation of bone", "Inflammation of bones", "bone disorder osteitis", "inflammatory bone disease", "bone inflammation disease", "bone inflammatory disease", "Inflammation of bone, NOS", "bone disease inflammatory", "Bone inflammatory disease", "inflammatory disorder of bone", "Inflammatory disorder of bone", "bone disorder inflammatory disease", "Bone inflammatory disease (disorder)", "bone inflammatory disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bone inflammation disease", "shortest_name_length": 8}
{"curie": "MONDO:0013490", "names": ["MLC2A", "megalencephalic leukoencephalopathy with subcortical cysts 2A", "MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2A", "megalencephalic leukoencephalopathy with subcortical cysts type 2A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "megalencephalic leukoencephalopathy with subcortical cysts 2A", "shortest_name_length": 5}
{"curie": "UMLS:C5205697", "names": ["Head and Neck Sebaceous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Head and Neck Sebaceous Carcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C0270330", "names": ["Developmental speech disorder", "SPEECH DISORDER DEVELOPMENTAL", "Speech disorder developmental", "developmental disorder speech", "developmental disorder; speech", "speech disorder; developmental", "developmental; speech disorder", "speech; developmental disorder", "Developmental speech disorder, NOS", "DSD - Developmental speech disorder", "Developmental speech disorder (disorder)", "Developmental speech disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Developmental speech disorder", "shortest_name_length": 29}
{"curie": "MONDO:0100034", "names": ["cerebral folate deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral folate deficiency", "shortest_name_length": 26}
{"curie": "UMLS:C0855150", "names": ["Stage III B-Lymphoblastic Lymphoma", "Stage III B Lymphoblastic Lymphoma", "Ann Arbor Stage III B Lymphoblastic Lymphoma", "Precursor B-Lymphoblastic Lymphoma Stage III", "Precursor B-lymphoblastic lymphoma stage III", "Stage III Precursor B-Lymphoblastic Lymphoma", "Precursor B-lymphoblastic lymphoma NOS stage III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Precursor B-lymphoblastic lymphoma stage III", "shortest_name_length": 34}
{"curie": "MONDO:0020291", "names": ["HYPOPLASTIC RIGHT HEART", "Hypoplastic right heart", "pseudotruncus arteriosus", "Pseudotruncus arteriosus", "Hypoplasia of right heart", "Underdeveloped right heart", "right hypoplastic heart syndrome", "hypoplasia; right heart syndrome", "Right hypoplastic heart syndrome", "right heart syndrome; hypoplasia", "Right Hypoplastic Heart Syndrome", "Hypoplastic Right Heart Syndrome", "Hypoplastic right heart syndrome", "hypoplastic right heart syndrome", "syndrome; hypoplastic right-heart", "syndrome; heart, hypoplastic right", "hypoplastic; right heart, syndrome", "syndrome; right heart, hypoplastic", "Hypoplasia of right heart (disorder)", "hypoplasia; heart, right heart syndrome", "heart; hypoplasia, right heart syndrome", "hypoplasia; heart, right heart (syndrome)", "heart; hypoplasia, right heart (syndrome)", "Right hypoplastic heart syndrome (disorder)", "hypoplastic right heart syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypoplastic right heart syndrome", "shortest_name_length": 23}
{"curie": "UMLS:C5446565", "names": ["Lacrimal Sac Diffuse Large B-Cell Lymphoma", "Lacrimal Drainage System Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lacrimal Drainage System Diffuse Large B-Cell Lymphoma", "shortest_name_length": 42}
{"curie": "MONDO:0032753", "names": ["SPAX9", "spastic ataxia 9, autosomal recessive", "SPASTIC ATAXIA 9, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic ataxia 9, autosomal recessive", "shortest_name_length": 5}
{"curie": "UMLS:C3898653", "names": ["TYPE 4C MYOCARDIAL INFARCTION", "Myocardial infarction type 4c", "Joint Task Force Type 4C Myocardial Infarction", "Joint ESC/ACCF/AHA/WHF Task Force Type 4C Myocardial Infarction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joint Task Force Type 4C Myocardial Infarction", "shortest_name_length": 29}
{"curie": "MONDO:0011281", "names": ["EAD", "CMS5", "Cms Ic", "CMS Ic", "CMS1C, FORMERLY", "CMS Ic, FORMERLY", "Cms Ic, formerly", "congenital myasthenic syndrome 5", "Congenital Myasthenic Syndrome 5", "MYASTHENIC SYNDROME, CONGENITAL, 5", "myasthenic syndrome, congenital, 5", "COLQ congenital myasthenic syndrome", "ENGEL CONGENITAL MYASTHENIC SYNDROME", "Engel congenital myasthenic syndrome", "Engel Congenital Myasthenic Syndrome", "congenital myasthenic syndrome type 5", "Congenital Myasthenic Syndrome Type Ic", "congenital myasthenic syndrome type Ic", "myasthenic syndrome, congenital, type 5", "endplate acetylcholinesterase deficiency", "Endplate Acetylcholinesterase Deficiency", "ENDPLATE ACETYLCHOLINESTERASE DEFICIENCY", "end plate acetylcholinesterase deficiency", "congenital myasthenic syndrome Engel type", "Myasthenic Syndrome, Congenital, Engel Type", "MYASTHENIC SYNDROME, CONGENITAL, ENGEL TYPE", "myasthenic syndrome, congenital, Engel type", "CONGENITAL MYASTHENIC SYNDROME TYPE Ic, FORMERLY", "congenital myasthenic syndrome type Ic, formerly", "ENDPLATE ACETYLCHOLINESTERASE DEFICIENCY (disorder)", "congenital myasthenic syndrome caused by mutation in COLQ"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myasthenic syndrome 5", "shortest_name_length": 3}
{"curie": "MONDO:0006668", "names": ["pink eye disease", "disease pink eye", "diseases eye pink", "purulent; ophthalmia", "ophthalmia; purulent", "conjunctivitis purulent", "purulent conjunctivitis", "Purulent conjunctivitis", "CONJUNCTIVITIS PURULENT", "Purulent Conjunctivitis", "conjunctivitis bacterial", "Conjunctivitis;bacterial", "bacterial conjunctivitis", "Bacterial Conjunctivitis", "Conjunctivitis bacterial", "Bacterial conjunctivitis", "CONJUNCTIVITIS BACTERIAL", "Conjunctivitis, Purulent", "Purulent Conjunctivitides", "Conjunctivitis, Bacterial", "Bacterial Conjunctivitides", "Conjunctivitides, Purulent", "Mucopurulent conjunctivitis", "MUCOPURULENT CONJUNCTIVITIS", "mucopurulent conjunctivitis", "Conjunctivitides, Bacterial", "Mucopurulent Conjunctivitis", "conjunctivitis mucopurulent", "Conjunctivitis bacterial NOS", "conjunctivitis; mucopurulent", "mucopurulent; conjunctivitis", "Conjunctivitis, Mucopurulent", "Mucopurulent Conjunctivitides", "Bacteria conjunctival disease", "Conjunctivitides, Mucopurulent", "Purulent conjunctivitis (disorder)", "Purulent conjunctivitis (diagnosis)", "Bacterial conjunctivitis (disorder)", "Bacteria caused conjunctival disease", "bacterial conjunctivitis (diagnosis)", "Mucopurulent conjunctivitis (disorder)", "mucopurulent conjunctivitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bacterial conjunctivitis", "shortest_name_length": 16}
{"curie": "MONDO:0013124", "names": ["PVOP2", "Pvop2", "PELVIC ORGAN PROLAPSE, SUSCEPTIBILITY TO, 2", "pelvic organ prolapse, susceptibility to, 2", "pelvic organ prolapse, susceptibility to, type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pelvic organ prolapse, susceptibility to, 2", "shortest_name_length": 5}
{"curie": "MONDO:0033012", "names": ["EKVP2", "erythrokeratodermia variabilis ET progressiva 2", "erythrokeratodermia variabilis et progressiva 2", "ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythrokeratodermia variabilis et progressiva 2", "shortest_name_length": 5}
{"curie": "UMLS:C4324336", "names": ["Hyperleukocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyperleukocytosis", "shortest_name_length": 17}
{"curie": "UMLS:C4724976", "names": ["Unresectable Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Sarcoma", "shortest_name_length": 20}
{"curie": "MONDO:0015820", "names": ["Cutaneous B-cell lymphoma", "CBCL - Cutaneous B-cell lymphoma", "Primary cutaneous B-cell lymphoma", "primary cutaneous B-cell lymphoma", "Primary cutaneous B-cell lymphoma (disorder)", "Primary cutaneous B-cell lymphoma (diagnosis)", "Primary cutaneous B-cell lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary cutaneous B-cell lymphoma", "shortest_name_length": 25}
{"curie": "MONDO:0020020", "names": ["visceral malformation of the liver, biliary tract, pancreas or spleen"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "visceral malformation of the liver, biliary tract, pancreas or spleen", "shortest_name_length": 69}
{"curie": "MONDO:0043103", "names": ["GDTH I", "iodide Transport defect", "Iodide Transport Defect", "Iodine transport defect", "Iodide transport defect", "iodine transport defect", "iodide transport defect", "iodide transport failure", "Iodide transport failure", "Iodine accumulation defect", "iodine accumulation defect", "Iodide transport defect (disorder)", "Genetic defect in thyroid hormonogenesis I", "Hypothyroidism due to iodide transport defect", "hypothyroidism due to iodide transport defect", "Hypothyroidism due to iodide concentration defect", "hypothyroidism due to iodide concentration defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypothyroidism due to iodide transport defect", "shortest_name_length": 6}
{"curie": "MONDO:0005418", "names": ["non-compaction cardiomyopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-compaction cardiomyopathy", "shortest_name_length": 29}
{"curie": "MONDO:0100289", "names": ["GOLDMANN-FAVRE SYNDROME", "Goldmann-Favre Syndrome", "Goldmann-Favre syndrome", "Enhanced S-cone syndrome", "Goldmann-Favre syndrome (disorder)", "Favre Hyaloideoretinal Degeneration", "FAVRE HYALOIDEORETINAL DEGENERATION", "Favre hyaloideoretinal Degeneration", "Retinoschisis with early nyctalopia", "retinoschisis with early nyctalopia", "RETINOSCHISIS WITH EARLY HEMERALOPIA", "Retinoschisis with Early Hemeralopia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Goldmann-Favre syndrome", "shortest_name_length": 23}
{"curie": "UMLS:C0391976", "names": ["pain syndrome", "PAIN SYNDROME", "pain disorder", "disorder pain", "syndrome pain", "Pain Disorder", "pain syndromes", "disorders pain", "pain disorders", "Pain Disorders", "Pain disease or syndrome", "pain syndromes (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pain Disorder", "shortest_name_length": 13}
{"curie": "MONDO:0005846", "names": ["microsporidiosis", "Microsporidioses", "Microsporidiosis", "Microsporidiasis", "Microspora Infection", "Microspora Infections", "Infection, Microspora", "Infections, Microspora", "infection by Microspora", "Microsporidia Infection", "Microsporidia infection", "Infection by Microspora", "Microsporidia Infections", "infection; Microsporidia", "Infection by Microsporea", "Infection, Microsporidia", "Microsporidia; infection", "infection by Microsporea", "Infections, Microsporidia", "infection by Microsporida", "Infection by Microsporida", "Infection by Microsporidia", "Infection by Cnidosporidia", "Infection by Microspora, NOS", "Infection by Cnidospora, NOS", "microsporidiosis (diagnosis)", "Infection by Microsporea, NOS", "Infection caused by Microspora", "Microsporidia infectious disease", "Microsporidia disease or disorder", "Infection caused by Microsporidia", "Microsporidia caused disease or disorder", "Infection caused by Microspora (disorder)", "Infection caused by Microsporidia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microsporidiosis", "shortest_name_length": 16}
{"curie": "MONDO:0044141", "names": ["Panic disorder without agoraphobia", "panic disorder without agoraphobia", "Panic Disorder without Agoraphobia", "Panic disorder without agoraphobia, NOS", "Panic disorder without agoraphobia (disorder)", "panic disorder without agoraphobia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "panic disorder without agoraphobia", "shortest_name_length": 34}
{"curie": "MONDO:0100133", "names": ["isolated complex I deficiency", "mitochondrial complex I deficiency", "Mitochondrial complex I deficiency", "NADH coenzyme Q reductase deficiency", "isolated NADH-CoQ reductase deficiency", "isolated NADH-ubiquinone reductase deficiency", "isolated NADH-coenzyme Q reductase deficiency", "complex 1 mitochondrial respiratory chain deficiency", "isolated mitochondrial respiratory chain complex I deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex I deficiency", "shortest_name_length": 29}
{"curie": "UMLS:C5207006", "names": ["Metastatic Appendix Mucinous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Appendix Mucinous Adenocarcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0019161", "names": ["PHA1", "PHA1B", "PHA type 1", "Pseudohypoaldosteronism Type 1", "Pseudohypoaldosteronism type 1", "Type I Pseudohypoaldosteronism", "Pseudohypoaldosteronism Type I", "pseudohypoaldosteronism type 1", "Type I, Pseudohypoaldosteronism", "Pseudohypoaldosteronism Type Is", "Pseudohypoaldosteronism, Type I", "Pseudohypoaldosteronism Type 1s", "Pseudohypoaldosteronism, type 1", "Type 1, Pseudohypoaldosteronism", "Type Is, Pseudohypoaldosteronism", "Pseudohypoaldosteronisms, Type I", "pseudohypoaldosteronism type 1 (diagnosis)", "Pseudohypoaldosteronism, type 1 (disorder)", "pseudohypoaldosteronism type I autosomal recessive", "Pseudohypoaldosteronism Type I Autosomal Recessive", "renal tubular disorder pseudohypoaldosteronism type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudohypoaldosteronism type 1", "shortest_name_length": 4}
{"curie": "UMLS:C5446582", "names": ["Locally Advanced Thyroid Gland Oncocytic Carcinoma", "Locally Advanced Thyroid Gland Hurthle Cell Carcinoma", "Locally Advanced Thyroid Gland Oncocytic (Hurthle Cell) Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Thyroid Gland Oncocytic Carcinoma", "shortest_name_length": 50}
{"curie": "UMLS:C0149663", "names": ["DEHISCENCE", "dehiscence", "Dehiscence", "dehiscences", "Dehiscence, NOS", "Organ Dehiscence", "Dehiscence (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dehiscence", "shortest_name_length": 10}
{"curie": "UMLS:C5419805", "names": ["Chromophobe Hepatocellular Carcinoma", "Chromophobe Hepatocellular Carcinoma with Abrupt Anaplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chromophobe Hepatocellular Carcinoma", "shortest_name_length": 36}
{"curie": "MONDO:0044738", "names": ["GADEVS", "Gabriele-De Vries syndrome", "Gabriele de Vries syndrome", "Gabriele-de Vries syndrome", "GABRIELE-DE VRIES SYNDROME", "Gabriele-de Vries Syndrome", "YY1 haploinsufficiency syndrome", "Gabriele-de Vries syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gabriele de Vries syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0024500", "names": ["duodenum NET", "duodenum neuroendocrine tumor", "duodenum neuroendocrine neoplasm", "duodenal neuroendocrine neoplasm", "neuroendocrine neoplasm of duodenum", "duodenum neuroendocrine tumor, well differentiated, low or intermediate grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "duodenal neuroendocrine neoplasm", "shortest_name_length": 12}
{"curie": "UMLS:C1260917", "names": ["Proteus pneumonia", "Pneumonia proteus", "Proteus; pneumonia", "pneumonia; Proteus", "Pneumonia due to proteus", "Proteus pneumonia (disorder)", "Proteus pneumonia (diagnosis)", "Proteus Gram negative pneumonia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Proteus pneumonia", "shortest_name_length": 17}
{"curie": "UMLS:C1336404", "names": ["Stage IVC Mouth Epidermoid Carcinoma", "Stage IVC Mouth Squamous Cell Carcinoma", "Stage IVC Epidermoid Carcinoma of Mouth", "Stage IVC Oral Cavity Squamous Cell Cancer", "Stage IVC Oral Cavity Epidermoid Carcinoma", "Stage IVC Squamous Cell Carcinoma of Mouth", "Stage IVC Epidermoid Carcinoma of the Mouth", "Stage IVC Oral Cavity Squamous Cell Carcinoma", "Stage IVC Epidermoid Carcinoma of Oral Cavity", "Stage IVC Squamous Cell Carcinoma of the Mouth", "Stage IVC Squamous Cell Carcinoma of Oral Cavity", "Stage IVC Epidermoid Carcinoma of the Oral Cavity", "Stage IVC Squamous Cell Carcinoma of the Oral Cavity", "Stage IVC Oral Cavity Squamous Cell Carcinoma AJCC v7", "Stage IVC Oral Cavity Squamous Cell Carcinoma AJCC v6", "Stage IVC Oral Cavity Squamous Cell Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Oral Cavity Squamous Cell Carcinoma AJCC v6 and v7", "shortest_name_length": 36}
{"curie": "UMLS:C1333818", "names": ["Gingival Angiofibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gingival Angiofibroma", "shortest_name_length": 21}
{"curie": "MONDO:0017187", "names": ["diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency", "hyperinsulinemic hypoglycemia due to SUR1 deficiency, diazoxide-resistant focal form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency", "shortest_name_length": 64}
{"curie": "UMLS:C0862638", "names": ["Recurrent Prostate Adenocarcinoma", "Adenocarcinoma of the prostate recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma of the prostate recurrent", "shortest_name_length": 33}
{"curie": "UMLS:C0272945", "names": ["brain laceration", "Brain Laceration", "Brain Lacerations", "Laceration, Brain", "brain lacerations", "laceration; brain", "brain; laceration", "Lacerations, Brain", "Laceration of brain", "Lacerating brain injury", "Laceration of brain, NOS", "Laceration of brain (disorder)", "Laceration of brain (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brain Lacerations", "shortest_name_length": 16}
{"curie": "MONDO:0019780", "names": ["ANOTIA", "anotia", "Anotia", "Anotias", "Absent ear", "ear; absent", "Absent ears", "Absence of auricle", "Absence of ear auricle", "Absence of external ear", "Agenesis of external ear", "Congenital auricle absence", "Congenital absence of pinna", "Congenital absence of auricle", "Congenital absence of pinna, NOS", "Congenital absence of ear auricle", "congenital absence of external ear", "Congenital absence of external ear", "Congenital absence of auricle, NOS", "Congenital absence of (ear) auricle", "Congenital absence of external ear (disorder)", "congenital absence of external ear (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anotia", "shortest_name_length": 6}
{"curie": "MONDO:0005937", "names": ["REM sleep disorder", "REM Behavior Disorder", "rem behavior disorder", "Behavior Disorder, REM", "REM Behavior Disorders", "Behavior Disorders, REM", "REM sleep behavior disorder", "rem behavior sleep disorder", "rem sleep behavior disorder", "REM Sleep Behavior Disorder", "behavior disorders rem sleep", "REM sleep behaviour disorder", "sleep disorder rem sleep behavior", "organic REM sleep behavior disorder", "REM sleep behavior disorder (diagnosis)", "Rapid eye movement sleep behavior disorder", "rapid eye movement sleep behavior disorder", "Rapid Eye Movement Sleep Behavior Disorder", "Rapid eye movement sleep behaviour disorder", "Behavior Disorder, Rapid Eye Movement Sleep", "organic REM sleep behavior disorder (diagnosis)", "Rapid eye movement sleep behavior disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "REM sleep behavior disorder", "shortest_name_length": 18}
{"curie": "MONDO:0008131", "names": ["Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant", "OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMAL DOMINANT", "optic atrophy, hearing loss, and peripheral neuropathy, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "optic atrophy, hearing loss, and peripheral neuropathy, autosomal dominant", "shortest_name_length": 74}
{"curie": "UMLS:C5400274", "names": ["Disseminated varicella zoster virus infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disseminated varicella zoster virus infection", "shortest_name_length": 45}
{"curie": "UMLS:C5206946", "names": ["Myopenia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myopenia", "shortest_name_length": 8}
{"curie": "MONDO:0009603", "names": ["HIBCHD", "HIBCH Deficiency", "HIBCH DEFICIENCY", "HIBCH deficiency", "methacrylic aciduria", "Methacrylic Aciduria", "METHACRYLIC ACIDURIA", "Methacrylic aciduria", "Valine Metabolic Defect", "valine metabolic defect", "VALINE METABOLIC DEFECT", "Valine metabolic defect", "METHACRYLIC ACID TOXICITY", "Methacrylic Acid Toxicity", "methacrylic acid toxicity", "3-hydroxyisobutryl-CoA hydrolase deficiency", "3-hydroxyisobutyryl-CoA hydrolase deficiency", "3-HYDROXYISOBUTYRYL-CoA HYDROLASE DEFICIENCY", "3-Hydroxyisobutyryl-CoA Hydrolase Deficiency", "3-@HYDROXYISOBUTYRYL-CoA HYDROLASE DEFICIENCY", "beta-hydroxyisobutyryl Coa deacylase deficiency", "BETA-HYDROXYISOBUTYRYL CoA DEACYLASE DEFICIENCY", "Beta-hydroxyisobutyryl-CoA deacylase deficiency", "Beta-Hydroxyisobutyryl CoA Deacylase Deficiency", "Deficiency of 3-hydroxyisobutyryl CoA hydrolase", "Deficiency of 3-hydroxyisobutyryl coenzyme A hydrolase", "Beta-hydroxyisobutyryl-coenzyme A deacylase deficiency", "Deficiency of 3-hydroxyisobutyryl coenzyme A hydrolase (disorder)", "Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency", "neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency", "Neurodegeneration due to 3-hydroxyisobutyryl coenzyme A hydrolase deficiency", "Neurodegeneration due to 3-hydroxyisobutyryl coenzyme A hydrolase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "3-hydroxyisobutyryl-CoA hydrolase deficiency", "shortest_name_length": 6}
{"curie": "MONDO:0011040", "names": ["Spinal Dysplasia, Anhalt Type", "spinal dysplasia, Anhalt type", "SPINAL DYSPLASIA, ANHALT TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal dysplasia, Anhalt type", "shortest_name_length": 29}
{"curie": "UMLS:C4725855", "names": ["Non-IgM MGUS", "Non-IgM Monoclonal Gammopathy of Undetermined Significance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-IgM Monoclonal Gammopathy of Undetermined Significance", "shortest_name_length": 12}
{"curie": "MONDO:0021542", "names": ["choroid angioma", "Choroid Angioma", "angioma of choroid", "choroid hemangioma", "Choroid Hemangioma", "Angioma of Choroid", "Choroidal hemangioma", "hemangioma of choroid", "Hemangioma of Choroid", "Choroidal haemangioma", "Hemangioma of choroid", "benign choroid angioma", "Benign Choroid Angioma", "Angioma of the Choroid", "Haemangioma of choroid", "angioma of the choroid", "Choroidal hemangiomata", "optic choroid hemangioma", "Hemangioma of the Choroid", "benign angioma of choroid", "Benign Angioma of Choroid", "benign choroid hemangioma", "hemangioma of the choroid", "Benign Choroid Hemangioma", "hemangioma, choroid, benign", "hemangioma of optic choroid", "Hemangioma, Choroid, Benign", "benign hemangioma of choroid", "Benign Hemangioma of Choroid", "benign angioma of the choroid", "Benign Angioma of the Choroid", "benign hemangioma of the choroid", "Hemangioma of choroid (disorder)", "Benign Hemangioma of the Choroid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemangioma of choroid", "shortest_name_length": 15}
{"curie": "UMLS:C2231324", "names": ["pulmonary brucellosis", "Pulmonary Brucelloses", "Pulmonary Brucellosis", "Brucellosis, Pulmonary", "Brucelloses, Pulmonary", "pulmonary brucellosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brucellosis, Pulmonary", "shortest_name_length": 21}
{"curie": "UMLS:C0280360", "names": ["Stage IV Mouth Verrucous Carcinoma", "Stage IV Verrucous Carcinoma of Mouth", "Stage IV Oral Cavity Verrucous Cancer", "Stage IV Oral Cavity Verrucous Carcinoma", "oral cavity verrucous carcinoma, stage IV", "Stage IV Verrucous Carcinoma of the Mouth", "oral cavity verrucous carcinoma, metastatic", "Stage IV Verrucous Carcinoma of Oral Cavity", "stage IV verrucous carcinoma of the oral cavity", "Verrucous carcinoma of the oral cavity stage IV", "Stage IV Verrucous Carcinoma of the Oral Cavity", "verrucous carcinoma of the oral cavity, stage IV", "metastatic verrucous carcinoma of the oral cavity", "verrucous carcinoma of the oral cavity, metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Verrucous carcinoma of the oral cavity stage IV", "shortest_name_length": 34}
{"curie": "UMLS:C0279918", "names": ["relapsed childhood HD", "pediatric HD, relapsed", "childhood HD, relapsed", "relapsed HD, childhood", "recurrent childhood HD", "recurrent pediatric HD", "recurrent HD, childhood", "HD, relapsed, childhood", "recurrent HD, pediatric", "childhood HD, recurrent", "refractory childhood HD", "HD, childhood, relapsed", "HD, childhood, recurrent", "HD, pediatric, recurrent", "HD, childhood, refractory", "Recurrent Hodgkin Lymphoma", "Relapsed Pediatric Hodgkin's Disease", "Relapsed Childhood Hodgkin's Disease", "relapsed pediatric Hodgkin's disease", "Recurrent Childhood Hodgkin Lymphoma", "relapsed childhood Hodgkin's disease", "relapsed Hodgkin's disease, childhood", "Relapsed Childhood Hodgkin's Lymphoma", "Relapsed Pediatric Hodgkin's Lymphoma", "Recurrent Childhood Hodgkin's Disease", "recurrent pediatric Hodgkin's disease", "pediatric Hodgkin's disease, relapsed", "childhood Hodgkin's disease, relapsed", "Recurrent Pediatric Hodgkin's Disease", "recurrent Hodgkin's disease, childhood", "Recurrent Pediatric Hodgkin's Lymphoma", "Recurrent Childhood Hodgkin's Lymphoma", "refractory childhood Hodgkin's disease", "lymphoma, relapsed childhood Hodgkin's", "Hodgkin's disease, relapsed, childhood", "Hodgkin's disease, recurrent, childhood", "Hodgkin's lymphoma, relapsed, childhood", "recurrent/refractory childhood Hodgkin lymphoma", "recurrent/refractory childhood Hodgkin's disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Hodgkin Lymphoma", "shortest_name_length": 21}
{"curie": "MONDO:0006163", "names": ["Serrated adenocarcinoma", "Colorectal Serrated Adenocarcinoma", "colorectal serrated adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorectal serrated adenocarcinoma", "shortest_name_length": 23}
{"curie": "MONDO:0019921", "names": ["UPD(6)pat", "paternal uniparental disomy of chromosome 6", "paternal uniparental disomy of chromosome type 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paternal uniparental disomy of chromosome 6", "shortest_name_length": 9}
{"curie": "UMLS:C5555760", "names": ["Ovarian Wolffian Tumor", "Wolffian Tumor of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Wolffian Tumor", "shortest_name_length": 22}
{"curie": "UMLS:C1334722", "names": ["Metastatic Meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Meningioma", "shortest_name_length": 21}
{"curie": "MONDO:0004492", "names": ["MEDIASTINITIS", "Mediastinitis", "mediastinitis", "Mediastinitides", "Mediastinum Inflammation", "mediastinitis (diagnosis)", "Mediastinum Inflammations", "Inflammation, Mediastinum", "Inflammations, Mediastinum", "Inflammatory disorder of mediastinum", "Inflammatory disorder of mediastinum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mediastinitis", "shortest_name_length": 13}
{"curie": "MONDO:0032807", "names": ["NEDVIBA", "NEURODEVELOPMENTAL DISORDER WITH VISUAL DEFECTS AND BRAIN ANOMALIES", "neurodevelopmental disorder with visual defects and brain anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with visual defects and brain anomalies", "shortest_name_length": 7}
{"curie": "UMLS:C0948344", "names": ["Escherichia urinary tract infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Escherichia urinary tract infection", "shortest_name_length": 35}
{"curie": "MONDO:0024354", "names": ["CMV Pneumonia", "CMV pneumonia", "cmv pneumonitis", "PNEUMONITIS CMV", "cytomegaloviral pneumonia", "cytomegalovirus pneumonia", "Pneumonia cytomegaloviral", "Cytomegaloviral Pneumonia", "Cytomegalovirus Pneumonia", "Cytomegaloviral pneumonia", "CYTOMEGALOVIRUS PNEUMONIA", "Cytomegalovirus pneumonia", "Cytomegaloviral pneumonitis", "cytomegalovirus pneumonitis", "Cytomegaloviral (CMV) pneumonia", "Cytomegalovirus caused pneumonia", "Cytomegaloviral pneumonia (disorder)", "Cytomegalic inclusion virus pneumonia", "cytomegalovirus pneumonia (diagnosis)", "cytomegalovirus pneumonitis (diagnosis)", "Pneumonia in cytomegalic inclusion disease", "pneumonia; cytomegaloviral disease (etiology)", "cytomegaloviral disease; pneumonia (etiology)", "cytomegaloviral disease; pneumonia (manifestation)", "pneumonia; cytomegaloviral disease (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cytomegalovirus pneumonia", "shortest_name_length": 13}
{"curie": "MONDO:0011002", "names": ["HMSN6A", "HMSN 6A", "Charcot-Marie-Tooth disease, type 6", "Charcot-Marie-Tooth disease, type 6A", "peripheral neuropathy and optic atrophy", "hereditary motor and sensory neuropathy VIA", "neuropathy, hereditary motor and sensory, type 6", "neuropathy, hereditary motor and sensory, type 6A", "neuropathy, hereditary motor and sensory, type VIA", "MFN2 hereditary motor and sensory neuropathy type 6", "hereditary motor and sensory neuropathy type 6 caused by mutation in MFN2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuropathy, hereditary motor and sensory, type 6A", "shortest_name_length": 6}
{"curie": "MONDO:0009931", "names": ["PULMONARY ATRESIA WITH INTACT VENTRICULAR SEPTUM", "Pulmonary Atresia with Intact Ventricular Septum", "Pulmonary atresia with intact ventricular septum", "pulmonary atresia with intact ventricular septum", "Pulmonary atresia-intact ventricular septum syndrome", "pulmonary atresia-intact ventricular septum syndrome", "Pulmonary Valve Atresia with Intact Ventricular Septum", "pulmonary valve atresia with intact ventricular septum", "PAIV - Pulmonary atresia with intact ventricular septum", "Pulmonary atresia with intact ventricular septum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary atresia-intact ventricular septum syndrome", "shortest_name_length": 48}
{"curie": "UMLS:C0333516", "names": ["Oncolysis", "oncolysis", "necrosis tumor", "tumor necrosis", "Tumor necrosis", "Tumour necrosis", "necrosis tumour", "tumour necrosis", "Necrosis, tumor", "Neoplasm necrosis", "Necrosis, neoplasm", "Tumor necrosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tumor necrosis", "shortest_name_length": 9}
{"curie": "MONDO:0002508", "names": ["Gingivitis", "GINGIVITIS", "gingivitis", "Gingivitides", "Inflamed gums", "Gingivitis NOS", "Gingivitis, NOS", "INFLAMMATION GUM", "gum inflammation", "Inflammation gum", "GINGIVITIS ACUTE", "Acute gingivitis", "acute gingivitis", "acute; gingivitis", "gingivitis; acute", "chronic gingivitis", "Inflammation of gum", "gingiva inflammation", "Red and swollen gums", "Acute gingivitis NOS", "Gingivitis (disorder)", "Gingival inflammation", "gingivitis (diagnosis)", "inflammation of gingiva", "Acute gingivitis (disorder)", "Acute gingival inflammation", "acute gingivitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gingivitis", "shortest_name_length": 10}
{"curie": "MONDO:0013061", "names": ["MFM6", "myofibrillar myopathy 6", "MYOPATHY, MYOFIBRILLAR, 6", "myopathy, myofibrillar, 6", "myofibrillar myopathy type 6", "myopathy, myofibrillar, type 6", "muscular dystrophy, Selcen type", "BAG3-related myofibrillar myopathy", "myopathy, myofibrillar, Bag3-related", "BAG3 myofibrillar myopathy (disease)", "Myopathy, Myofibrillar, Bag3-Related", "myofibrillar myopathy (disease) caused by mutation in BAG3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myofibrillar myopathy 6", "shortest_name_length": 4}
{"curie": "UMLS:C0751954", "names": ["Venous Brain Infarction", "Brain Venous Infarction", "Venous Brain Infarctions", "Infarction, Venous Brain", "Brain Venous Infarctions", "Brain Infarction, Venous", "Venous Infarction, Brain", "Infarction, Brain Venous", "Infarctions, Venous Brain", "Brain Infarctions, Venous", "Infarctions, Brain Venous", "Venous Infarctions, Brain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Venous Infarction, Brain", "shortest_name_length": 23}
{"curie": "UMLS:C1262064", "names": ["Oculogyration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oculogyration", "shortest_name_length": 13}
{"curie": "MONDO:0060533", "names": ["MISSLA", "MICROCEPHALY, SHORT STATURE, AND LIMB ABNORMALITIES", "microcephaly, short stature, and limb abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly, short stature, and limb abnormalities", "shortest_name_length": 6}
{"curie": "MONDO:0001792", "names": ["Epiphora due to insufficient drainage", "epiphora due to insufficient drainage", "Epiphora due to insufficient drainage (disorder)", "epiphora due to insufficient drainage (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epiphora due to insufficient drainage", "shortest_name_length": 37}
{"curie": "UMLS:C5418264", "names": ["Chronic Lower Respiratory System Disorder", "Non-Neoplastic Chronic Lower Respiratory System Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Chronic Lower Respiratory System Disorder", "shortest_name_length": 41}
{"curie": "UMLS:C4521058", "names": ["Stage IB Vulvar Cancer", "stage IB vulvar cancer", "Stage IB Vulvar Carcinoma", "stage IB vulvar carcinoma", "stage IB vulvar cancer AJCC v7", "Stage IB Vulvar Cancer AJCC v7", "stage IB vulvar carcinoma AJCC v7", "Stage IB Vulvar Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Vulvar Cancer AJCC v7", "shortest_name_length": 22}
{"curie": "UMLS:C1696849", "names": ["Dermo-hypodermitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dermo-hypodermitis", "shortest_name_length": 18}
{"curie": "MONDO:0007529", "names": ["eps", "EPS", "Miescher", "MIESCHER ELASTOMA", "Miescher elastoma", "elastoma; Miescher", "Miescher; elastoma", "elastosis perforans", "Elastosis perforans", "Miescher's elastoma", "Perforating elastoma", "PERFORATING ELASTOSIS", "LUTZ-MIESCHER DISEASE", "Perforating elastosis", "Elastosis perforans serpiginosa", "elastosis perforans serpiginosa", "ELASTOSIS PERFORANS SERPIGINOSA", "elastosis; perforans serpiginosa", "perforans serpiginosa; elastosis", "Perforating serpiginous elastosis", "Keratosis follicularis serpiginosa", "follicularis; keratosis, serpiginosa", "keratosis; follicularis, serpiginosa", "Elastosis perforans serpiginosa (disorder)", "elastosis perforans serpiginosa (diagnosis)", "elastoma Intrapapillare perforans verruciformis", "ELASTOMA INTRAPAPILLARE PERFORANS VERRUCIFORMIS", "Elastoma intrapapillare perforans verruciformis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "elastosis perforans serpiginosa", "shortest_name_length": 3}
{"curie": "MONDO:0060758", "names": ["SCA42ND", "spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits", "SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits", "shortest_name_length": 7}
{"curie": "MONDO:0021655", "names": ["Secondary catabolic mucinosis of skin", "secondary catabolic mucinosis of skin", "Secondary catabolic mucinosis of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary catabolic mucinosis of skin", "shortest_name_length": 37}
{"curie": "UMLS:C0242785", "names": ["food drug interaction", "interaction drug food", "drug-food interaction", "food-drug interaction", "drug interaction food", "Food-Drug Interaction", "Drug-Food Interaction", "drug food interaction", "drug-food interactions", "Food Drug Interactions", "food drug interactions", "drugs food interaction", "Interaction, Drug-Food", "drug foods interaction", "Drug-Food Interactions", "drug food interactions", "Interaction, Food-Drug", "Food-Drug Interactions", "food-drug interactions", "Drug Food Interactions", "DRUG - FOOD INTERACTION", "drugs food interactions", "Interactions, Drug-Food", "Interactions, Food-Drug", "drugs foods interactions", "drug nutrient interaction", "nutrient drug interaction", "interaction drug nutrient", "drugs interaction nutrient", "Drug-nutrient interactions", "drug interactions nutrient", "Food interaction with drug", "drug interaction with food", "Drug interaction with food", "drugs interaction nutrients", "drugs interactions nutrient", "Medication interaction with food", "Drug interaction with food (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Food-Drug Interactions", "shortest_name_length": 21}
{"curie": "MONDO:0008797", "names": ["Edentia", "Anodontia", "anodontia", "Agomphosis", "Anodontism", "Agomphiasis", "Teeth absent", "Teeth missing", "missing teeth", "teeth; absent", "Anodontia, NOS", "Anodontia vera", "Tooth Agenesis", "absence; teeth", "Total anodontia", "Dental Agenesis", "Anodontism, NOS", "Missing all teeth", "Agenesis of teeth", "Congenital edentia", "Complete anodontia", "Anodontia (disorder)", "Congenital edentia, NOS", "Complete dental agenesis", "complete absence of teeth", "Complete absence of teeth", "Total absence of all teeth", "absence of permanent teeth", "congenital absence of teeth", "Congenital absence of teeth", "teeth, permanent, absence of", "Complete agenesis of all teeth", "developmental absence of tooth", "Developmental absence of tooth", "anodontia of permanent dentition", "Congenital absence of teeth, NOS", "Failure of development of all teeth", "Congenital complete absence of teeth", "Complete congenital absence of teeth", "congenital absence of teeth (diagnosis)", "Complete developmental absence of teeth", "Developmental absence of tooth (disorder)", "total anodontia of permanent and deciduous teeth", "Total anodontia of permanent and deciduous teeth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anodontia", "shortest_name_length": 7}
{"curie": "UMLS:C1859040", "names": ["MCKD2", "ADMCKD2", "ADTKD-UMOD", "UMOD-related ADTKD", "Medullary Cystic Kidney Disease 2", "Medullary cystic kidney disease 2", "Uromodulin-associated kidney disease", "Medullary cystic kidney disease type 2", "Medullary Cystic Kidney Disease Type 2", "medullary cystic kidney disease - MCKD2", "Familial juvenile hyperuricemic nephropathy type 1", "medullary cystic kidney disease - MCKD2 (diagnosis)", "Medullary Cystic Kidney Disease 2, Autosomal Dominant", "UMOD-related autosomal dominant tubulointerstitial kidney disease", "Autosomal dominant medullary cystic kidney disease with hyperuricemia", "Autosomal dominant medullary cystic kidney disease with hyperuricaemia", "Uromodulin related autosomal dominant tubulointerstitial kidney disease", "Uromodulin related autosomal dominant tubulointerstitial kidney disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Medullary Cystic Kidney Disease Type 2", "shortest_name_length": 5}
{"curie": "MONDO:0018356", "names": ["secondary neonatal autoimmune disease", "Transplacentally acquired neonatal autoimmune disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary neonatal autoimmune disease", "shortest_name_length": 37}
{"curie": "UMLS:C3272519", "names": ["Small Intestinal Retention Polyp", "Juvenile Polyp of the Small Intestine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Juvenile Polyp of the Small Intestine", "shortest_name_length": 32}
{"curie": "MONDO:0017012", "names": ["partial trisomy of chromosome 1p", "partial duplication of chromosome 1p", "partial duplication of the short arm of chromosome 1", "partial duplication of the short arm of chromosome type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of the short arm of chromosome 1", "shortest_name_length": 32}
{"curie": "UMLS:C3840252", "names": ["Pseudomyogenic Hemangioendothelioma", "Epithelioid Sarcoma-Like Hemangioendothelioma", "Pseudomyogenic (Epithelioid Sarcoma-Like) Hemangioendothelioma", "Pseudomyogenic (epithelioid sarcoma-like) hemangioendothelioma", "Pseudomyogenic (epithelioid sarcoma-like) haemangioendothelioma", "Pseudomyogenic (epithelioid sarcoma-like) hemangioendothelioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pseudomyogenic (epithelioid sarcoma-like) hemangioendothelioma", "shortest_name_length": 35}
{"curie": "MONDO:0001076", "names": ["prediabetes", "Latent diabetes", "latent diabetes", "latent; diabetes", "diabetes; latent", "diabetes chemical", "chemical diabetes", "Chemical diabetes", "diabetes; chemical", "chemicals diabetes", "Intolerance;glucose", "Glucose intolerance", "glucose intolerance", "GLUCOSE INTOLERANCE", "Glucose Intolerance", "chemicals; diabetes", "glucose: intolerance", "Intolerance, Glucose", "intolerance; glucose", "Glucose Intolerances", "glucose; intolerance", "Intolerances, Glucose", "Glucose malabsorption", "glucose malabsorption", "malabsorption; glucose", "glucose: malabsorption", "glucose; malabsorption", "prediabetes (diagnosis)", "Malabsorption of glucose", "malabsorption of glucose", "glucose impaired tolerance", "impaired glucose tolerance", "Impaired;glucose tolerance", "GLUCOSE TOLERANCE ABNORMAL", "Glucose tolerance abnormal", "Impaired Glucose Tolerance", "Glucose tolerance impaired", "Abnormal glucose tolerance", "Impaired glucose tolerance", "abnormal; glucose tolerance", "Glucose Tolerance, Impaired", "Impaired Glucose Tolerances", "Tolerance, Impaired Glucose", "Glucose Tolerances, Impaired", "Tolerances, Impaired Glucose", "glucose; tolerance, abnormal", "Glucose Intolerance (disease)", "Impaired glucose tolerance, NOS", "glucose intolerance (diagnosis)", "Prediabetic nonclinical diabetes", "IGT - Impaired glucose tolerance", "Malabsorption of glucose (disorder)", "Impaired glucose tolerance (disorder)", "impaired glucose tolerance (diagnosis)", "glucose: [intolerance] or [malabsorption]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glucose intolerance", "shortest_name_length": 11}
{"curie": "MONDO:0003187", "names": ["Bartholin gland adenoid cystic carcinoma", "Bartholin Gland Adenoid Cystic Carcinoma", "Bartholin's Gland Adenoid Cystic Carcinoma", "Bartholin's gland adenoid cystic carcinoma", "major vestibular gland adenoid cystic carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bartholin gland adenoid cystic carcinoma", "shortest_name_length": 40}
{"curie": "UMLS:C5555296", "names": ["Current_HepB_infection", "Current Hep B Infection", "Current Hepatitis B Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Current Hepatitis B Infection", "shortest_name_length": 22}
{"curie": "UMLS:C2064435", "names": ["Extrahepatic Bile Duct Kaposi Sarcoma", "Kaposi's sarcoma of extrahepatic bile duct", "Kaposi's sarcoma of extrahepatic bile duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kaposi's sarcoma of extrahepatic bile duct", "shortest_name_length": 37}
{"curie": "UMLS:C2242575", "names": ["Compulsive shopping"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Compulsive shopping", "shortest_name_length": 19}
{"curie": "MONDO:0007987", "names": ["Kniest Syndrome", "Kniest syndrome", "kniest syndrome", "Kniest dysplasia", "kniest dysplasia", "KNIEST DYSPLASIA", "Kniest Dysplasia", "Kniest chondrodystrophy", "Kniest Chondrodystrophy", "Kniest dysplasia (disorder)", "Swiss cheese cartilage dysplasia", "Swiss Cheese Cartilage Dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kniest dysplasia", "shortest_name_length": 15}
{"curie": "MONDO:0035112", "names": ["AML with BCR-ABL1", "AML with t(9;22)(q34.1;q11.2)", "Acute Myeloid Leukemia with BCR-ABL1", "Acute myeloid leukemia with BCR-ABL1", "acute myeloid leukemia with BCR-ABL1", "Acute myeloid leukaemia with BCR-ABL1", "Acute myeleoid leukemia with BCR-ABL1", "Provisional Entity: AML with BCR-ABL1", "Acute myeloid leukemia with BCR-ABL1 (disorder)", "acute myeloid leukemia with t(9;22)(q34.1;q11.2)", "Acute myeloid leukemia with t(9;22)(q34.1;q11.2)", "Acute myeloid leukaemia with t(9;22)(q34.1;q11.2)", "Acute myeloid leukemia with BCR-ABL1 (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia with BCR-ABL1", "shortest_name_length": 17}
{"curie": "MONDO:0010770", "names": ["UBE1Y", "Ube1Y", "ubiquitin-activating enzyme, Y-linked", "UBIQUITIN-ACTIVATING ENZYME, Y-LINKED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ubiquitin-activating enzyme, Y-linked", "shortest_name_length": 5}
{"curie": "UMLS:C3898069", "names": ["Osteolytic Lesions of Multiple Myeloma", "osteolytic lesions of multiple myeloma", "Osteolytic Lesions of Multiple Myeloma/Plasma Cell Myeloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Osteolytic Lesions of Multiple Myeloma", "shortest_name_length": 38}
{"curie": "MONDO:0011748", "names": ["USH1G", "USH1G Usher syndrome", "Usher syndrome type 1G", "Usher syndrome type Ig", "Usher syndrome type IG", "Usher Syndrome, Type IG", "USHER syndrome, type Ig", "Usher syndrome, type 1G", "USHER SYNDROME, TYPE IG", "Usher syndrome caused by mutation in USH1G"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Usher syndrome type 1G", "shortest_name_length": 5}
{"curie": "MONDO:0008884", "names": ["Oculoosteocutaneous Syndrome", "oculoosteocutaneous syndrome", "OCULOOSTEOCUTANEOUS SYNDROME", "Oculoosteocutaneous syndrome", "Anodontia-Hypotrichosis Syndrome", "ANODONTIA-HYPOTRICHOSIS SYNDROME", "anodontia-hypotrichosis syndrome", "Oculoosteocutaneous syndrome (disorder)", "brachymetapody anodontia hypotrichosis albinoidism", "BRACHYMETAPODY-ANODONTIA-HYPOTRICHOSIS-ALBINOIDISM", "BRACHYMETAPODY-anodontia-hypotrichosis-ALBINOIDISM", "Brachymetapody-Anodontia-Hypotrichosis-Albinoidism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculoosteocutaneous syndrome", "shortest_name_length": 28}
{"curie": "UMLS:C1336103", "names": ["Stage 0a Urethra Cancer", "Urethra Cancer Stage 0a", "Stage 0a Urethral Cancer", "Stage 0a Urethra Carcinoma", "Stage 0a Urethral Carcinoma", "Stage 0a Carcinoma of Urethra", "Stage 0a Urethral Cancer AJCC v7", "Stage 0a Carcinoma of the Urethra"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0a Urethral Cancer AJCC v7", "shortest_name_length": 23}
{"curie": "MONDO:0007387", "names": ["Cdl", "CDLS1", "De Lange syndrome", "de Lange syndrome 1", "Cornelia de Lange 1", "Brachmann-De Lange syndrome", "Cornelia de Lange syndrome 1", "Cornelia de Lange Syndrome 1", "CORNELIA DE LANGE SYNDROME 1", "Cornelia DE Lange syndrome 1", "Lange syndrome 1 Amsterdam dwarf", "NIPBL Cornelia de Lange syndrome", "Cornelia De Lange syndrome type 1", "typus Degenerativus Amstelodamensis", "Cornelia de Lange (CDL) syndrome (CLS) 1", "Cornelia de Lange syndrome caused by mutation in NIPBL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cornelia de Lange syndrome 1", "shortest_name_length": 3}
{"curie": "MONDO:0012048", "names": ["MDD", "melancholia", "clinical depression", "unipolar depression", "Depression;endogenous", "ENDOGENOUS DEPRESSION", "Depression endogenous", "DEPRESSION ENDOGENOUS", "Endogenous depression", "Endogenous Depression", "depression endogenous", "endogenous depression", "depression; endogenous", "melancholic depression", "Endogenous Depressions", "endogenous; depression", "Depression, Endogenous", "Depressions, Endogenous", "major depressive disorder", "Endogenous depression (disorder)", "Endogenous depression (diagnosis)", "major depressive disorder with melancholic features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endogenous depression", "shortest_name_length": 3}
{"curie": "UMLS:C5447391", "names": ["Recurrent Lung Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Lung Neuroendocrine Neoplasm", "shortest_name_length": 38}
{"curie": "UMLS:C5420333", "names": ["Sialolipoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sialolipoma", "shortest_name_length": 11}
{"curie": "UMLS:C1511267", "names": ["Borderline Ovarian Serous Cystadenofibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Ovarian Serous Cystadenofibroma", "shortest_name_length": 42}
{"curie": "MONDO:0008557", "names": ["TCPT", "11q23 Deletion Disorder", "Paris-Trousseau Syndrome", "Deletion Disorder, 11q23", "Paris Trousseau Syndrome", "Paris-Trousseau syndrome", "Jacobsen Thrombocytopenia", "Thrombocytopenia, Jacobsen", "Paris-Trousseau thrombocytopenia", "Paris-Trousseau Thrombocytopenia", "Paris Trousseau Thrombocytopenia", "Thrombocytopenia, Paris-Trousseau", "chromosome 11q23 deletion syndrome", "CHROMOSOME 11q23 DELETION SYNDROME", "thrombocytopenia Paris-Trousseau type", "Paris-Trousseau Type Thrombocytopenia", "Type Thrombocytopenia, Paris-Trousseau", "Thrombocytopenia, Paris-Trousseau Type", "THROMBOCYTOPENIA, PARIS-TROUSSEAU TYPE", "Paris-Trousseau Type Thrombocytopenias", "Thrombocytopenia, Paris Trousseau Type", "thrombocytopenia, Paris-TROUSSEAU type", "Paris-Trousseau thrombocytopenia (diagnosis)", "thrombocytopenia, Paris-Trousseau type, Isolated cases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paris-Trousseau thrombocytopenia", "shortest_name_length": 4}
{"curie": "UMLS:C1333387", "names": ["Endocrine Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endocrine Syndrome", "shortest_name_length": 18}
{"curie": "MONDO:0016197", "names": ["qualitative or quantitative defects of selenoprotein N1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of selenoprotein N1", "shortest_name_length": 55}
{"curie": "UMLS:C2242582", "names": ["Cholestatic liver injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cholestatic liver injury", "shortest_name_length": 24}
{"curie": "MONDO:0017687", "names": ["disorder of neutral amino acid transport", "inborn neutral amino acid transport disorder", "inborn error of neutral amino acid transport", "rare inborn error of neutral amino acid transport"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of neutral amino acid transport", "shortest_name_length": 40}
{"curie": "UMLS:C4054716", "names": ["Infundibular Stenosis", "Infundibular Stenosis of the Calyces of the Kidney"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infundibular Stenosis", "shortest_name_length": 21}
{"curie": "UMLS:C0751220", "names": ["Inappropriate ACTH Secretion Syndrome", "Inappropriate Adrenocorticotropic Hormone Secretion", "Adrenocorticotropic Hormone, Inappropriate Secretion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Inappropriate ACTH Secretion Syndrome", "shortest_name_length": 37}
{"curie": "MONDO:0004024", "names": ["Spinal Cord Neuroblastoma", "spinal cord neuroblastoma", "Neuroblastoma of Spinal Cord", "neuroblastoma of spinal cord", "Neuroblastoma of the Spinal Cord", "neuroblastoma of the spinal cord", "neuroblastoma of the Spinal Cord", "neuroblastoma of spinal cord (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal cord neuroblastoma", "shortest_name_length": 25}
{"curie": "UMLS:C3658301", "names": ["Mycoplasma Induced Stevens Johnson Syndrome", "Mycoplasma-Induced Stevens Johnson Syndrome", "Mycoplasma-Induced Stevens-Johnson Syndrome", "Stevens-Johnson Syndrome, Mycoplasma-Induced", "Syndrome, Mycoplasma-Induced Stevens-Johnson"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mycoplasma-Induced Stevens-Johnson Syndrome", "shortest_name_length": 43}
{"curie": "MONDO:0005850", "names": ["PARAVACCINA", "PSEUDOCOWPOX", "Milker Nodes", "PARAVACCINIA", "Pseudocowpox", "paravaccinia", "pseudocowpox", "Paravaccinia", "milker's node", "Milker's node", "Milkers' node", "milker nodule", "Milker's Node", "Milkers Nodes", "milkers' node", "Milker's nodes", "Milker's Nodes", "Node, Milker's", "milker's nodule", "Nodes, Milker's", "Milker's nodule", "Milker's nodules", "MILKER'S NODULES", "milker's nodules", "Poxvirus Infection", "poxvirus infection", "Poxviridae disease", "Infection, Poxvirus", "Pox virus infection", "Poxvirus Infections", "Infections, Poxvirus", "Poxviridae Infection", "Poxviridae Infections", "Infection, Poxviridae", "Infections, Poxviridae", "Poxvirus infection, NOS", "Pseudocowpox (disorder)", "paravaccinia (diagnosis)", "Paravaccinia, unspecified", "Disease due to Poxviridae", "DISEASES DUE TO POXVIRIDAE", "Disease caused by Poxviridae", "Milker's nodules (diagnosis)", "poxvirus infection (diagnosis)", "Poxvirus infections, unspecified", "DISEASES DUE TO UNASSIGNED POXVIRIDAE", "Disease caused by Poxviridae (disorder)", "Disease due to unassigned Poxviridae, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "milker's nodule", "shortest_name_length": 11}
{"curie": "MONDO:0009402", "names": ["AFFND2", "Naguib syndrome", "AFFN dysostosis 2", "AFFN DYSOSTOSIS 2", "Naguib Richieri Costa syndrome", "NAGUIB-RICHIERI-COSTA SYNDROME", "Naguib-Richieri-Costa syndrome", "acrofrontofacionasal dysostosis 2", "ACROFRONTOFACIONASAL DYSOSTOSIS 2", "Acrofrontofacionasal Dysostosis 2", "acrofrontofacionasal syndrome type 2", "Acrofrontofacionasal syndrome type 2", "acrofrontofacionasal dysostosis type 2", "Acrofrontofacionasal dysostosis type 2", "acrofrontofacionasal dysostosis, severe", "Acrofrontofacionasal dysostosis, severe", "Acro-fronto-facio-nasal dysostosis type 2", "Hypertelorism-hypospadias-polysyndactyly syndrome", "Hypertelorism hypospadias polysyndactyly syndrome", "hypertelorism hypospadias polysyndactyly syndrome", "Acrofrontofacionasal dysostosis type 2 (disorder)", "hypertelorism-hypospadias-polysyndactyly syndrome", "Hypertelorism, hypospadias, polysyndactyly syndrome", "hypertelorism, hypospadias, and polysyndactyly syndrome", "Hypertelorism, Hypospadias, and Polysyndactyly Syndrome", "HYPERTELORISM, HYPOSPADIAS, AND POLYSYNDACTYLY SYNDROME", "ACROFRONTOFACIONASAL DYSOSTOSIS WITH GENITOURINARY ANOMALIES", "acrofrontofacionasal dysostosis with genitourinary anomalies", "Acrofrontofacionasal Dysostosis with Genitourinary Anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acrofrontofacionasal dysostosis 2", "shortest_name_length": 6}
{"curie": "UMLS:C0333513", "names": ["Fibrinoid necrosis", "Fibrinoid Necrosis", "fibrinoid necrosis", "Necrosis, fibrinoid", "fibrinoid degeneration", "Fibrinoid degeneration", "Fibrinoid necrosis (morphologic abnormality)", "Fibrinoid degeneration (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fibrinoid necrosis", "shortest_name_length": 18}
{"curie": "MONDO:0010712", "names": ["PHPX", "pituitary dwarfism IV", "panhypopituitarism X-linked", "X-linked panhypopituitarism", "Panhypopituitarism X-linked", "PANHYPOPITUITARISM, X-LINKED", "panhypopituitarism, X-linked", "Panhypopituitarism, X-Linked", "Panhypopituitarism - X-linked", "pituitary dwarfism IV, formerly", "PITUITARY DWARFISM IV, FORMERLY", "pituitary dwarfism IV (formerly)", "X-linked panhypopituitarism (disorder)", "Panhypopituitarism, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "panhypopituitarism, X-linked", "shortest_name_length": 4}
{"curie": "MONDO:0700104", "names": ["respiratory system disorder, non-human animal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "respiratory system disorder, non-human animal", "shortest_name_length": 45}
{"curie": "UMLS:C4727410", "names": ["Recurrent Appendix Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Appendix Carcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0007202", "names": ["blepharoptosis myopia ectopia lentis", "Blepharoptosis myopia ectopia lentis", "BLEPHAROPTOSIS, MYOPIA, AND ECTOPIA LENTIS", "blepharoptosis, myopia, and ectopia lentis", "Blepharoptosis, Myopia, and Ectopia Lentis", "Blepharoptosis-myopia-ectopia lentis syndrome", "blepharoptosis-myopia-ectopia lentis syndrome", "Blepharoptosis, myopia, ectopia lentis syndrome", "Blepharoptosis, myopia, ectopia lentis syndrome (disorder)", "Dominantly inherited blepharoptosis, high myopia, and ectopia lentis", "dominantly inherited blepharoptosis, high myopia, and ectopia lentis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blepharoptosis-myopia-ectopia lentis syndrome", "shortest_name_length": 36}
{"curie": "UMLS:C4727170", "names": ["Metastatic Chordoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Chordoma", "shortest_name_length": 19}
{"curie": "MONDO:0012349", "names": ["SCOD3", "SCDO3", "spondylocostal dysostosis 3", "autosomal recessive spondylocostal dysostosis 3", "Spondylocostal Dysostosis 3, Autosomal Recessive", "SPONDYLOCOSTAL DYSOSTOSIS 3, AUTOSOMAL RECESSIVE", "SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 3", "spondylocostal dysostosis 3, autosomal recessive", "LFNG autosomal recessive spondylocostal dysostosis", "autosomal recessive spondylocostal dysostosis caused by mutation in LFNG"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondylocostal dysostosis 3, autosomal recessive", "shortest_name_length": 5}
{"curie": "MONDO:0043683", "names": ["Leriche", "Saddle embolus", "Leriche Syndrome", "syndrome leriche", "leriche syndrome", "LERICHE SYNDROME", "Leriche syndrome", "syndrome, Leriche", "Syndrome, Leriche", "Leriches syndrome", "Leriches Syndrome", "leriches syndrome", "Leriche's syndrome", "leriche's syndrome", "Leriche's Syndrome", "Syndrome, Leriche's", "syndrome, Leriche's", "saddle embolus; aorta", "aorta; saddle embolus", "Aortoiliac obstruction", "Saddle embolus of aorta", "aorta; embolism, saddle", "EMBOLISM, AORTIC, SADDLE", "embolism; aortic, saddle", "Aortic bifurcation embolus", "Aortic bifurcation syndrome", "aorta; embolism, bifurcation", "syndrome; aortic bifurcation", "Leriche syndrome (diagnosis)", "aorta; bifurcation, syndrome", "aortic bifurcation; syndrome", "EMBOLISM, AORTIC BIFURCATION", "bifurcation; aortic, syndrome", "embolism; aortic, bifurcation", "Leriche's syndrome (disorder)", "aorta; thrombosis, bifurcation", "thrombosis; aortic, bifurcation", "AORTIC OCCLUSION DISTAL CHRONIC", "Saddle embolus of aorta syndrome", "saddle embolus of abdominal aorta", "Saddle embolus of abdominal aorta", "AORTIC BIFURCATION SYNDROME, ACUTE", "AORTIC BIFURCATION SYNDROME, CHRONIC", "Aortic bifurcation embolus (disorder)", "Aortic bifurcation thrombosis syndrome", "Chronic aorto-iliac occlusion syndrome", "Saddle embolus (morphologic abnormality)", "saddle embolus of abdominal aorta (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leriche syndrome", "shortest_name_length": 7}
{"curie": "MONDO:0004760", "names": ["urethral false passage", "Urethral false passage", "FP - False passage in the urethra", "Urethral false passage (disorder)", "urethral false passage (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urethral false passage", "shortest_name_length": 22}
{"curie": "UMLS:C3888593", "names": ["Administration site extravasation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Administration site extravasation", "shortest_name_length": 33}
{"curie": "MONDO:0000309", "names": ["aniseikonia", "Aniseikonia", "Aniseikonia (disorder)", "aniseikonia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aniseikonia", "shortest_name_length": 11}
{"curie": "UMLS:C5239334", "names": ["Localized Pancreatic Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized Pancreatic Adenocarcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C5447318", "names": ["Congenital Phagocytic Defect", "Congenital Phagocytic Disease", "Congenital Phagocytic Disorder", "Congenital Defect of Phagocyte", "Congenital Defects of Phagocytes", "Congenital Defects of Phagocyte Number, Function, or Both"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Defects of Phagocyte Number, Function, or Both", "shortest_name_length": 28}
{"curie": "MONDO:0004949", "names": ["Mature B-Cell Neoplasm", "Mature B-cell neoplasm", "mature B-cell neoplasm", "mature B-cell neoplasms", "neoplasm of mature B-cells", "mature B-cell lymphocytic neoplasm", "Mature B-Cell Lymphocytic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplasm of mature B-cells", "shortest_name_length": 22}
{"curie": "MONDO:0015485", "names": ["primary glaucoma", "primary hereditary glaucoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary hereditary glaucoma", "shortest_name_length": 16}
{"curie": "UMLS:C0587240", "names": ["Bone erosion", "bone erosion", "Bony erosion", "erosion; bone", "bone; erosion", "Erosion of bone", "Erosion of bone (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Erosion of bone", "shortest_name_length": 12}
{"curie": "UMLS:C0750466", "names": ["YEAST INFECTION", "Yeast infection", "yeast infection", "infection; yeast", "Yeast Infections", "Yeast infections", "yeast; infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Yeast infection", "shortest_name_length": 15}
{"curie": "UMLS:C1335898", "names": ["Salivary Gland Cystadenoma", "cystadenoma of salivary gland", "cystadenoma of salivary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cystadenoma of salivary gland", "shortest_name_length": 26}
{"curie": "UMLS:C0853662", "names": ["Estrogen deficiency", "deficiency estrogen", "estrogen deficiency", "Oestrogen deficiency", "oestrogen deficiency", "deficiencies estrogen"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Estrogen deficiency", "shortest_name_length": 19}
{"curie": "MONDO:0003194", "names": ["lung hemangioma", "hemangioma of lung", "pulmonary hemangioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemangioma of lung", "shortest_name_length": 15}
{"curie": "UMLS:C1142110", "names": ["Abdominal Compartment Syndrome", "Abdominal compartment syndrome", "compartment syndrome abdominal", "abdominal compartment syndrome", "Compartment Syndrome, Abdominal", "Abdominal Compartment Syndromes", "Syndrome, Abdominal Compartment", "Compartment Syndromes, Abdominal", "Syndromes, Abdominal Compartment", "Abdominal compartment syndrome (disorder)", "Abdominal compartment syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abdominal Compartment Syndrome", "shortest_name_length": 30}
{"curie": "MONDO:0020372", "names": ["early-onset sutural cataract", "early-onset cataract with Y-shaped suture opacities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early-onset sutural cataract", "shortest_name_length": 28}
{"curie": "MONDO:0007877", "names": ["LAP", "Laryngeal Adductor Paralysis", "LARYNGEAL ADDUCTOR PARALYSIS", "Laryngeal adductor paralysis", "laryngeal adductor paralysis", "Congenital laryngeal adductor palsy", "Vocal Cord Dysfunction, Adductor Type", "vocal cord dysfunction, adductor type", "VOCAL CORD DYSFUNCTION, ADDUCTOR TYPE", "Congenital laryngeal adductor paralysis", "Congenital laryngeal adductor palsy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laryngeal adductor paralysis", "shortest_name_length": 3}
{"curie": "MONDO:0015487", "names": ["Fatal infantile COX deficiency", "fatal infantile COX deficiency", "fatal infantile encephalomyopathy", "fatal infantile encephalocardiomyopathy", "Fatal infantile cytochrome C oxidase deficiency", "fatal infantile cytochrome C oxidase deficiency", "COX deficiency, infantile mitochondrial myopathy", "Fatal infantile cytochrome C oxidase deficiency (disorder)", "fatal infantile cardioencephalomyopathy due to cytochrome C oxidase deficiency", "Fatal infantile cardioencephalomyopathy due to cytochrome C oxidase deficiency", "fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency", "cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fatal infantile encephalocardiomyopathy", "shortest_name_length": 30}
{"curie": "UMLS:C0267925", "names": ["bile duct stenosi", "bile duct stenosis", "Bile Duct Stenosis", "Bile duct stenosis", "stenosis; bile duct", "bile duct; stenosis", "Choledochus stenosis", "Hepatic duct stenosis", "Stenosis of bile duct", "hepatic duct stenosis", "of bile duct stenosis", "Stenosis of bile duct (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bile Duct Stenosis", "shortest_name_length": 17}
{"curie": "UMLS:C0036094", "names": ["salivary gland fistula", "Salivary Gland Fistula", "Salivary gland fistula", "Fistula, Salivary Gland", "Salivary Gland Fistulas", "Gland Fistula, Salivary", "salivary gland; fistula", "Gland Fistulas, Salivary", "Fistulas, Salivary Gland", "Fistula of salivary gland", "fistula of salivary gland", "Fistula of salivary gland (disorder)", "fistula of salivary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Salivary Gland Fistula", "shortest_name_length": 22}
{"curie": "UMLS:C4687430", "names": ["Mediastinal/Thymic NMC", "Mediastinal/Thymic NUT Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mediastinal/Thymic NUT Carcinoma", "shortest_name_length": 22}
{"curie": "UMLS:C0267094", "names": ["Esophagobronchial Fistula", "Bronchoesophageal fistula", "Esophagobronchial fistula", "bronchoesophageal fistula", "ESOPHAGO BRONCHIAL FISTULA", "Oesophagobronchial fistula", "fistula; esophagobronchial", "esophagobronchial; fistula", "broncho-esophageal fistula", "fistula; bronchoesophageal", "Broncho-esophageal fistula", "Broncho-Esophageal Fistula", "bronchoesophageal; fistula", "FISTULA, BRONCHOESOPHAGEAL", "broncho-oesophageal fistula", "Broncho-oesophageal fistula", "BOF - Broncho-esophageal fistula", "BOF - Broncho-oesophageal fistula", "Bronchoesophageal fistula (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Broncho-esophageal fistula", "shortest_name_length": 25}
{"curie": "MONDO:0017413", "names": ["RLS", "Reunion island Larsen syndrome", "multiple joint dislocations-short stature-hyperlaxity-craniofacial dysmorphism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reunion island Larsen syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0008446", "names": ["PRM4", "SPERM PROTAMINE P4", "sperm protamine P4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sperm protamine P4", "shortest_name_length": 4}
{"curie": "MONDO:0005109", "names": ["HIV", "HIV disease", "HIV DISEASE", "HIV INFECTION", "Infection;HIV", "HIV Infection", "HIV infection", "hiv infection", "HIV Infections", "Infection, HIV", "HIV infections", "Infections, HIV", "HIV infection NOS", "HTLV-III Infection", "HTLV III Infections", "Infection, HTLV-III", "HTLV-III Infections", "Infections, HTLV-III", "HIV disease; infection", "HTLV-III-LAV Infection", "HIV infectious disease", "HTLV III LAV Infections", "HTLV-III-LAV Infections", "Infection, HTLV-III-LAV", "Infections, HTLV-III-LAV", "Human Immunodeficiency Virus", "infection; HIV disease as cause", "lymphadenopathy-associated virus", "HIV seropositivity or positivity", "Human immunodeficiency virus disease", "immunodeficiency virus disease; human", "human immunodeficiency virus; disease", "Human immunodeficiency virus syndrome", "Human Immunodeficiency Virus Infection", "DISEASES DUE TO IMMUNODEFICIENCY VIRUS", "Human immunodeficiency virus infection", "Human immunodeficiency virus [HIV] disease", "Human immunodeficiency virus infection, NOS", "human immunodeficiency virus (HIV) infection", "HIV - Human immunodeficiency virus infection", "lymphadenopathy-associated virus (diagnosis)", "HUMAN IMMUNODEFICIENCY VIRUS [HIV] INFECTION", "T-Lymphotropic Virus Type III Infections, Human", "T Lymphotropic Virus Type III Infections, Human", "Human immunodeficiency virus infectious disease", "human immunodeficiency virus infectious disease", "Human immunodeficiency virus disease or disorder", "Human immunodeficiency virus [HIV] disease (B20)", "human T-lymphotropic virus 3 (HTLV-III) infection", "disease (or disorder); resulting from HIV disease", "Human immunodeficiency virus infection (disorder)", "HIV disease; disease (i.e. caused by HIV disease)", "Unspecified human immunodeficiency virus [HIV] disease", "Human immunodeficiency virus caused disease or disorder", "human immunodeficiency virus (HIV) infection (diagnosis)", "human T-lymphotropic virus 3 (HTLV-III) infection (diagnosis)", "disease (or disorder); HIV disease (resulting from HIV disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HIV infectious disease", "shortest_name_length": 3}
{"curie": "UMLS:C1334748", "names": ["Methotrexate-Associated Hodgkin Lymphoma", "Methotrexate-Associated Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Methotrexate-Associated Hodgkin Lymphoma", "shortest_name_length": 40}
{"curie": "MONDO:0010501", "names": ["MRXSML", "MRXS34", "mental retardation, X-linked, syndromic 34", "MENTAL RETARDATION, X-LINKED, SYNDROMIC 34", "syndromic X-linked intellectual disability 34", "NONO X-linked syndromic intellectual disability", "mental retardation, X-linked, syndromic type 34", "intellectual disability, X-linked, syndromic 34", "syndromic X-linked intellectual disability type 34", "intellectual disability, X-linked, syndromic type 34", "intellectual developmental disorder, X-linked syndromic 34", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 34", "syndromic X-linked mental retardation Mircsof-Langouet type", "MENTAL RETARDATION, X-LINKED, SYNDROMIC, MIRCSOF-LANGOUET TYPE", "mental retardation, X-linked, syndromic, Mircsof-Langouet type", "syndromic X-linked intellectual disability Mircsof-Langouet type", "intellectual disability, X-linked, syndromic, Mircsof-Langouet type", "X-linked syndromic intellectual disability caused by mutation in NONO", "macrocephaly-intellectual disability-left ventricular non compaction syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic X-linked intellectual disability 34", "shortest_name_length": 6}
{"curie": "MONDO:0011046", "names": ["Short stature Brussels type", "short stature, Brussels type", "Short stature, Brussels type", "Mievis-Verellen-Dumoulin syndrome", "Mievis Verellen-Dumoulin syndrome", "Mievis Verellen Dumoulin syndrome", "Short stature syndrome, Brussels type", "short stature syndrome, Brussels type", "SHORT STATURE SYNDROME, BRUSSELS TYPE", "Short stature Brussels type (disorder)", "familial short stature with facial dysmorphism and osteochondrodysplastic lesions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short stature, Brussels type", "shortest_name_length": 27}
{"curie": "MONDO:0022454", "names": ["angiosarcoma of the scalp", "scalp angiosarcoma (disease)", "angiosarcoma (disease) of scalp"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angiosarcoma of the scalp", "shortest_name_length": 25}
{"curie": "MONDO:0000645", "names": ["Benign Fallopian Tube Tumor", "benign fallopian tube tumor", "FALLOPIAN TUBE TUMOR BENIGN", "Fallopian Tube Tumor, Benign", "fallopian tube tumor, benign", "benign tumor of fallopian tube", "Benign fallopian tube neoplasm", "benign fallopian tube neoplasm", "fallopian tube benign neoplasm", "Benign Tumor of Fallopian Tube", "Benign Fallopian Tube Neoplasm", "Benign tumor of fallopian tube", "Fallopian Tube Neoplasm, Benign", "Benign tumor of fallopian tubes", "Benign tumour of fallopian tube", "fallopian tube neoplasm, benign", "benign tumor of fallopian tubes", "Benign Neoplasm of Fallopian Tube", "Benign neoplasm of fallopian tube", "benign neoplasm of fallopian tube", "benign tumor of the fallopian tube", "Benign Tumor of the Fallopian Tube", "benign neoplasm of the fallopian tube", "Benign Neoplasm of the Fallopian Tube", "Benign neoplasm of fallopian tube (disorder)", "benign neoplasm of fallopian tube (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fallopian tube benign neoplasm", "shortest_name_length": 27}
{"curie": "UMLS:C4331477", "names": ["Unresectable Osteosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Osteosarcoma", "shortest_name_length": 25}
{"curie": "MONDO:0001363", "names": ["absolute glaucoma", "Blind hypertensive eye", "blind hypertensive eye", "BLIND HYPERTENSIVE EYE", "Blind hypertensive eye (disorder)", "Blind hypertensive eye (diagnosis)", "disorders of globe degenerative blind hypertensive eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blind hypertensive eye", "shortest_name_length": 17}
{"curie": "MONDO:0022321", "names": ["2-Methylacetoacetyl CoA thiolase deficiency", "2-methylacetoacetyl CoA thiolase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "2-methylacetoacetyl CoA thiolase deficiency", "shortest_name_length": 43}
{"curie": "UMLS:C5420436", "names": ["Maxillofacial Chondroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Maxillofacial Chondroblastoma", "shortest_name_length": 29}
{"curie": "MONDO:0015883", "names": ["Halal-Setton-Wang syndrome", "Halal Setton Wang syndrome", "Hidrotic ectodermal dysplasia Halal type", "hidrotic ectodermal dysplasia Halal type", "Hidrotic ectodermal dysplasia, Halal type", "hidrotic ectodermal dysplasia, Halal type", "Hidrotic ectodermal dysplasia Halal type (disorder)", "Ectodermal dysplasia with skin anomaly and intellectual disability", "ectodermal dysplasia with skin anomalies and intellectual disability", "Trichodysplasia-abnormal dermatoglyphics-intellectual disability syndrome", "trichodysplasia-abnormal dermatoglyphics-intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hidrotic ectodermal dysplasia, Halal type", "shortest_name_length": 26}
{"curie": "UMLS:C3897032", "names": ["GBS Infection, Late-Onset", "Group B Streptococcal Infection, Late-Onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Group B Streptococcal Infection, Late-Onset", "shortest_name_length": 25}
{"curie": "UMLS:C0919872", "names": ["Drug Exposure via Breast Milk", "Drug Exposure Via Breast Milk", "Drug exposure via breast milk", "Transmission of drug via breast milk"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drug exposure via breast milk", "shortest_name_length": 29}
{"curie": "MONDO:0006256", "names": ["BRCA", "Invasive Breast Cancer", "invasive breast cancer", "breast cancer invasive", "Invasive Breast Carcinoma", "invasive breast carcinoma", "Invasive breast carcinoma", "Invasive mammary carcinoma", "Breast cancer invasive NOS", "Invasive Mammary Carcinoma", "infiltrating breast cancer", "invasive mammary carcinoma", "Invasive Carcinoma of Breast", "Invasive carcinoma of breast", "invasive carcinoma of breast", "Infiltrating Breast Carcinoma", "infiltrating breast carcinoma", "Infiltrating Carcinoma of Breast", "Invasive Carcinoma of the Breast", "invasive carcinoma of the breast", "infiltrating carcinoma of breast", "infiltrating carcinoma of the breast", "Infiltrating Carcinoma of the Breast", "Invasive carcinoma of breast (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "invasive breast carcinoma", "shortest_name_length": 4}
{"curie": "UMLS:C1335005", "names": ["Non-Neoplastic Dental Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Dental Disorder", "shortest_name_length": 30}
{"curie": "MONDO:0022055", "names": ["Calabro syndrome", "craniosynostosis, limb abnormalities, brevicollis, micrognathia, pulmonary stenosis, and genital defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Calabro syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0019408", "names": ["Astley-Kendall syndrome", "Astley-Kendall dysplasia", "Astley-Kendall dysplasia (disorder)", "short limbed dwarfism with extensive stippling", "Short limbed dwarfism with extensive stippling"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Astley-Kendall dysplasia", "shortest_name_length": 23}
{"curie": "MONDO:0035642", "names": ["MPAL with t(v;11q23.3); MLL rearranged", "MPAL with t(v;11q23.3); KMT2A rearranged", "mixed phenotype acute leukemia with t(v;11q23.3)", "Mixed Phenotype Acute Leukemia with t(v;11q23); MLL Rearranged", "Mixed phenotype acute leukemia with t(v;11q23); MLL rearranged", "Mixed phenotype acute leukaemia with t(v;11q23); MLL rearranged", "Mixed Phenotype Acute Leukemia with t(v;11q23.3); MLL Rearranged", "Mixed Phenotype Acute Leukemia with t(v;11q23.3); KMT2A Rearranged", "Mixed phenotype acute leukemia with t(v;11q23); MLL rearranged (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed phenotype acute leukemia with t(v;11q23.3)", "shortest_name_length": 38}
{"curie": "MONDO:0019315", "names": ["DCM", "Diffuse Cutaneous Mastocytosis", "Diffuse cutaneous mastocytosis", "diffuse cutaneous mastocytosis", "Mastocytosis, Diffuse Cutaneous", "Cutaneous Mastocytoses, Diffuse", "MASTOCYTOSIS, DIFFUSE CUTANEOUS", "Cutaneous Mastocytosis, Diffuse", "Diffuse cutaneous mastocytosis (diagnosis)", "Diffuse cutaneous maculopapulous mastocytosis", "diffuse cutaneous maculopapulous mastocytosis", "Diffuse cutaneous mastocytosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diffuse cutaneous mastocytosis", "shortest_name_length": 3}
{"curie": "MONDO:0001281", "names": ["Alternating Exotropia", "Alternating exotropia", "alternating exotropia", "Alternating strabismus", "Exotropia, alternating", "Exotropia, Alternating", "Strabismus, alternating", "Alternating exotropia, NOS", "Alternating exotropia (disorder)", "alternating exotropia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alternating exotropia", "shortest_name_length": 21}
{"curie": "MONDO:0000750", "names": ["Tooth Abscess", "Dental sepsis", "Tooth abscess", "dental sepsis", "tooth abscess", "abscess tooth", "DENTAL ABSCESS", "abscess; tooth", "teeth; abscess", "abscess dental", "dental abscess", "Dental abscess", "Abscess;dental", "Abscess dental", "Tooth abscesses", "abscesses tooth", "abscessed tooth", "Dental abscesses", "abscesses dental", "Dentoalveolar abscess", "Dental abscess (disorder)", "oral tissue abscess dental", "Dental abscess (diagnosis)", "tooth abscess (physical finding)", "DENTAL ABSCESS PERIAPICAL OR PERIODONTAL", "DENTAL ABSCESS <PERIAPICAL OR PERIODONTAL>"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dental abscess", "shortest_name_length": 13}
{"curie": "MONDO:0014759", "names": ["MRT51", "mental retardation, autosomal recessive 51", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 51", "intellectual disability, autosomal recessive 51", "mental retardation, autosomal recessive type 51", "intellectual disability, autosomal recessive type 51", "autosomal recessive intellectual developmental disorder 51", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 51", "intellectual developmental disorder, autosomal recessive 51", "HNMT autosomal recessive non-syndromic intellectual disability", "autosomal recessive non-syndromic intellectual disability caused by mutation in HNMT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 51", "shortest_name_length": 5}
{"curie": "UMLS:C5420304", "names": ["Unresectable Peritoneal Epithelioid Mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Peritoneal Epithelioid Mesothelioma", "shortest_name_length": 48}
{"curie": "MONDO:0022934", "names": ["Lafer Davis syndrome", "Davis Lafer syndrome", "Mental retardation unusual facies Davis Lafer type", "mental retardation unusual facies Davis Lafer type", "intellectual disability unusual facies Davis Lafer type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Davis Lafer syndrome", "shortest_name_length": 20}
{"curie": "MONDO:0007998", "names": ["Microspherophakia-metaphyseal dysplasia", "MICROSPHEROPHAKIA-METAPHYSEAL DYSPLASIA", "microspherophakia-metaphyseal dysplasia", "Verloes Van Maldergem Marneffe syndrome", "Verloes-Van Maldergem-de Marneffe syndrome", "microspherophakia-metaphyseal dysplasia syndrome", "dominantly inherited bone dysplasia with severe eye involvement", "Dominantly inherited bone dysplasia with severe eye involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microspherophakia-metaphyseal dysplasia syndrome", "shortest_name_length": 39}
{"curie": "MONDO:0016927", "names": ["Duplication of chromosome 6", "partial trisomy of chromosome 6", "Partial trisomy of chromosome 6", "Partial duplication of chromosome 6", "partial duplication of chromosome 6", "partial duplication of chromosome type 6", "Partial trisomy of chromosome 6 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of chromosome 6", "shortest_name_length": 27}
{"curie": "UMLS:C5418884", "names": ["Advanced Malignant Mixed Mesodermal (Mullerian) Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Malignant Mixed Mesodermal (Mullerian) Tumor", "shortest_name_length": 53}
{"curie": "MONDO:0015771", "names": ["mosaic trisomy 7", "Mosaic trisomy 7", "Trisomy 7 mosaicism", "trisomy 7 mosaicism", "Mosaic trisomy type 7", "Mosaic trisomy 7 syndrome", "Mosaic trisomy chromosome 7", "Chromosome 7, trisomy mosaic", "trisomy 7 mosaicism (diagnosis)", "Mosaic trisomy 7 syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mosaic trisomy 7", "shortest_name_length": 16}
{"curie": "MONDO:0020703", "names": ["erythroid tumor", "Erythroid Tumor", "Erythroid Neoplasm", "erythroid neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythroid neoplasm", "shortest_name_length": 15}
{"curie": "MONDO:0006225", "names": ["stomach mantle cell lymphoma", "Gastric Mantle Cell Lymphoma", "gastric mantle cell lymphoma", "mantle cell lymphoma of stomach", "Mantle Cell Lymphoma of Stomach", "mantle cell lymphoma of the stomach", "Mantle Cell Lymphoma of the Stomach", "mantle cell lymphoma of stomach (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric mantle cell lymphoma", "shortest_name_length": 28}
{"curie": "UMLS:C0729958", "names": ["lung transplant rejection", "Lung transplant rejection", "rejection lung transplant", "lung transplant; rejection", "rejection; transplant, lung(s)", "Lung transplant rejection (disorder)", "lung transplant rejection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung transplant rejection", "shortest_name_length": 25}
{"curie": "MONDO:0010030", "names": ["SS", "ss", "SICCA", "Sjögren", "Sjogren's", "sicca syndrome", "Sicca Syndrome", "SICCA SYNDROME", "Sicca syndrome", "SYNDROME SICCA", "Syndrome sicca", "Syndrome, Sicca", "syndrome; sicca", "sicca; syndrome", "xerodermosteosis", "sjogren syndrome", "Sjögren Syndrome", "Sjogren syndrome", "Sjogren Syndrome", "SJOGREN SYNDROME", "syndrome sjogren", "Sjögren syndrome", "sjogrens syndrome", "Sjogren's disease", "syndrome sjogrens", "sjogren's disease", "Sjogrens Syndrome", "SJOEGREN SYNDROME", "Sjögren's disease", "Sjogrens syndrome", "SJOGRENS SYNDROME", "Sjogren's syndrome", "SJOGREN'S SYNDROME", "sjogren's syndrome", "Sjogren's Syndrome", "Syndrome Sjogren's", "Sjögren's syndrome", "Sjögren's Syndrome", "SYNDROME SJOGREN'S", "sjoegren's syndrome", "sjogrens's syndrome", "sjogren's syndromes", "syndrome, Sjogren's", "Sjoegren's syndrome", "Syndrome, Sjogren's", "Sicca syndrome [Sjogren]", "primary Sjögren syndrome", "Sjögren-Gougerot syndrome", "GOUGEROUT-SJOEGREN SYNDROME", "Sjogren syndrome (diagnosis)", "Sjögren's syndrome (disorder)", "Dacryosialoadenopathy syndrome", "Gougerot-Mulock-Houwer syndrome", "primary Sjögren-Gougerot syndrome", "primary Sjogren-Gougerot syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sjogren syndrome", "shortest_name_length": 2}
{"curie": "MONDO:0000668", "names": ["autotopagnosia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autotopagnosia", "shortest_name_length": 14}
{"curie": "UMLS:C1879898", "names": ["Breast Nevus", "Nevus of Breast", "Nevus of the Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Nevus", "shortest_name_length": 12}
{"curie": "UMLS:C0853347", "names": ["Venous thrombosis limb", "Venous thrombosis (limbs)", "Venous thrombosis NOS limb", "Venous thrombosis NOS (limbs)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Venous thrombosis limb", "shortest_name_length": 22}
{"curie": "MONDO:0000400", "names": ["mixed cerebral palsy", "Mixed Cerebral Palsy", "Mixed cerebral palsy", "Cerebral Palsy, Mixed", "Mixed Cerebral Palsies", "paralysis; cerebral, mixed", "cerebral; paralysis, mixed", "Mixed cerebral palsy (disorder)", "mixed cerebral palsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed cerebral palsy", "shortest_name_length": 20}
{"curie": "UMLS:C1336908", "names": ["Endometrial Endometrioid Adenocarcinoma with Clear Cell Change"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endometrial Endometrioid Adenocarcinoma with Clear Cell Change", "shortest_name_length": 62}
{"curie": "MONDO:0010400", "names": ["SPM", "X-linked SPMD", "X-linked scapuloperoneal syndrome", "SCAPULOPERONEAL MYOPATHY, FHL1-RELATED", "scapuloperoneal myopathy, FHL1-related", "Scapuloperoneal Myopathy, FHL1-Related", "scapuloperoneal myopathy, X-linked dominant", "SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT", "Scapuloperoneal Myopathy, X-Linked Dominant", "X-linked scapuloperoneal muscular dystrophy", "scapuloperoneal myopathy, X-linked dominant, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked scapuloperoneal muscular dystrophy", "shortest_name_length": 3}
{"curie": "UMLS:C0560570", "names": ["Cardiovascular Injury", "Cardiovascular injury", "cardiovascular injury", "Cardiovascular injuries", "Cardiovascular injury (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiovascular injury", "shortest_name_length": 21}
{"curie": "MONDO:0004260", "names": ["perforate peptic ulcer", "Perforated Peptic Ulcer", "PERFORATED PEPTIC ULCER", "peptic perforated ulcer", "Perforated peptic ulcer", "PEPTIC ULCER PERFORATED", "perforated peptic ulcer", "Peptic ulcer perforated", "perforation peptic ulcer", "Peptic ulcer perforation", "peptic ulcer perforation", "Peptic Ulcer Perforation", "peptic perforation ulcer", "peptic perforated ulcers", "ulcer peptic perforation", "Peptic Ulcer Perforations", "Perforation, Peptic Ulcer", "Ulcer Perforation, Peptic", "Perforations, Peptic Ulcer", "Ulcer Perforations, Peptic", "Peptic ulcer with perforation", "Ulcer peptic with perforation", "ULCER PEPTIC WITH PERFORATION", "Peptic ulcers and perforation", "peptic ulcer with perforation", "PEPTIC ULCER WITH PENETRATION", "peptic; ulcer, with perforation", "ulcer; peptic, with perforation", "Peptic ulcer, NOS with perforation", "Acute peptic ulcer with perforation", "acute peptic ulcer with perforation", "Peptic ulcer, acute with perforation", "ulcer; peptic, acute, with perforation", "Peptic ulcer with perforation (disorder)", "peptic ulcer with perforation (diagnosis)", "Acute peptic ulcer with perforation (disorder)", "acute peptic ulcer with perforation (diagnosis)", "Acute peptic ulcer, site unspecified, with perforation", "Acute peptic ulcer of unspecified site with perforation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peptic ulcer perforation", "shortest_name_length": 22}
{"curie": "MONDO:0016509", "names": ["MPPC syndrome", "microcornea posterior megalolenticonus persistent fetal vasculature coloboma", "microcornea-posterior megalolenticonus-persistent fetal vasculature-coloboma syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcornea-posterior megalolenticonus-persistent fetal vasculature-coloboma syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0003260", "names": ["Adult Cerebellar Tumor", "adult cerebellar tumor", "Adult Cerebellar Tumors", "adult cerebellar tumors", "tumor of adult Cerebellum", "adult cerebellar neoplasm", "Adult Cerebellar Neoplasm", "tumor of adult cerebellum", "Tumor of Adult Cerebellum", "Adult Cerebellar Neoplasms", "adult cerebellar neoplasms", "Neoplasm of Adult Cerebellum", "neoplasm of adult cerebellum", "Tumor of the Adult Cerebellum", "cerebellar neoplasm of adults", "tumor of the adult cerebellum", "Neoplasm of the Adult Cerebellum", "neoplasm of the adult cerebellum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult cerebellar neoplasm", "shortest_name_length": 22}
{"curie": "MONDO:0000947", "names": ["Psychosexual Problem", "Psychosexual disorder", "Psychosexual problems", "problem; psychosexual", "psychosexual; problem", "psychosexual disorder", "Psychosexual Disorder", "Disorder, Psychosexual", "Psychosexual Disorders", "disorder; psychosexual", "PSYCHOSEXUAL DISORDERS", "psychosexual; disorder", "Psychosexual disorders", "psychosexual disorders", "Disorders, Psychosexual", "Psychosexual Dysfunction", "psychosexual dysfunction", "Psychosexual Dysfunctions", "Psychosexual disorder NOS", "Dysfunction, Psychosexual", "Psychosexual disorder, NOS", "Dysfunctions, Psychosexual", "sexual; disorder, nonorganic", "disorder; sexual, nonorganic", "sexual disorder psychosexual", "Non-organic sexual dysfunction", "non-organic sexual dysfunction", "Psychological Sexual Dysfunction", "Psychosexual disease or syndrome", "Psychosexual disorder (disorder)", "Psychological Sexual Dysfunctions", "psychosexual disorder (diagnosis)", "Sexual Dysfunction, Psychological", "Unspecified psychosexual disorder", "Dysfunction, Psychological Sexual", "Dysfunctions, Psychological Sexual", "Sexual Dysfunctions, Psychological", "Psychosexual dysfunction with other specified psychosexual dysfunctions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "psychosexual disorder", "shortest_name_length": 20}
{"curie": "MONDO:0024498", "names": ["GLM", "GLM1", "ependymoma", "astrocytoma", "subependymoma", "oligodendroglioma", "glioblastoma, somatic", "glioblastoma multiforme", "glioma susceptibility 1", "GLIOMA SUSCEPTIBILITY 1", "GLIOMA OF BRAIN, FAMILIAL", "Glioma of Brain, Familial", "glioma of brain, familial", "glioma, susceptibility to, somatic", "glioma susceptibility 1, autosomal dominant, somatic mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glioma susceptibility 1", "shortest_name_length": 3}
{"curie": "MONDO:0006561", "names": ["eyelid hypopigmentation", "hypopigmentation of eyelid", "Hypopigmentation of eyelid", "Hypopigmentation of eyelid (disorder)", "hypopigmentation of eyelid (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eyelid hypopigmentation", "shortest_name_length": 23}
{"curie": "UMLS:C4764230", "names": ["Refractory Spindle Cell Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Spindle Cell Sarcoma", "shortest_name_length": 31}
{"curie": "UMLS:C1328289", "names": ["Bladder tamponade", "Bladder thrombotic tamponade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder tamponade", "shortest_name_length": 17}
{"curie": "UMLS:C1335775", "names": ["Retroperitoneal Ganglioneuroma", "Ganglioneuroma of Retroperitoneum", "Ganglioneuroma of the Retroperitoneum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retroperitoneal Ganglioneuroma", "shortest_name_length": 30}
{"curie": "MONDO:0013749", "names": ["VSD3", "ventricular septal defect 3", "VENTRICULAR SEPTAL DEFECT 3", "ventricular septal defect type 3", "ventricular septal defect - VSD3", "NKX2-5 ventricular septal defect (disease)", "ventricular septal defect - VSD3 (diagnosis)", "ventricular septal defect (disease) caused by mutation in NKX2-5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ventricular septal defect 3", "shortest_name_length": 4}
{"curie": "MONDO:0011317", "names": ["Microcephaly, Severe, with Skeletal Anomalies including Posterior Rib-Gap Defects", "microcephaly, severe, with skeletal anomalies including posterior rib-Gap defects", "MICROCEPHALY, SEVERE, WITH SKELETAL ANOMALIES INCLUDING POSTERIOR RIB-GAP DEFECTS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly, severe, with skeletal anomalies including posterior rib-Gap defects", "shortest_name_length": 81}
{"curie": "UMLS:C0267853", "names": ["cholelithiasis cholecystitis", "cholecystitis cholelithiasis", "Cholecystitis/cholelithiasis", "cholelithiasis; cholecystitis", "cholecystitis; cholelithiasis", "Cholecystitis and cholelithiasis", "Cholelithiasis with cholecystitis", "cholelithiasis with cholecystitis", "Cholecystitis with Cholelithiasis", "choledocholithiasis; cholecystitis", "cholecystitis; choledocholithiasis", "cholelithiasis; with cholecystitis", "cholecystitis; gallbladder calculus", "Biliary calculus with cholecystitis", "Cholecystitis with cholelithiasis NOS", "Choledocolithiasis with cholecystitis", "Cholelithiasis with cholecystitis NOS", "Bile duct calculus with cholecystitis", "choledocholithiasis with cholecystitis", "Choledocholithiasis with cholecystitis", "bile duct; calculus with cholecystitis", "Cholelithiasis with cholecystitis, NOS", "Calculus of bile duct with cholecystitis", "Biliary calculus with cholecystitis, NOS", "calculus; gallbladder, with cholecystitis", "Calculus of gallbladder with cholecystitis", "calculus of gallbladder with cholecystitis", "d.choledochus; calculus, with cholecystitis", "Calculus of any bile duct with cholecystitis", "cholelithiasis with cholecystitis (diagnosis)", "Calculus of bile duct with cholecystitis, NOS", "Calculus of gallbladder with cholecystitis, NOS", "choledocholithiasis with cholecystitis (diagnosis)", "Calculus of bile duct with cholecystitis (disorder)", "Calculus of gallbladder with cholecystitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Calculus of gallbladder with cholecystitis", "shortest_name_length": 28}
{"curie": "MONDO:0004001", "names": ["compartment syndrome", "Compartment syndrome", "COMPARTMENT SYNDROME", "Compartment Syndrome", "Compartment syndromes", "compartment; syndrome", "syndrome; compartment", "compartment syndromes", "Compartment Syndromes", "Compartmental syndrome", "compartmental syndrome", "compartmental syndromes", "Compartment syndrome NOS", "Compartment syndrome, NOS", "Compartmental syndrome, NOS", "Compartment syndrome (disorder)", "compartment syndrome (diagnosis)", "Compartment syndrome, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "compartment syndrome", "shortest_name_length": 20}
{"curie": "MONDO:0018916", "names": ["isolated anorectal malformation", "nonsyndromic anorectal malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated anorectal malformation", "shortest_name_length": 31}
{"curie": "MONDO:0016884", "names": ["partial monosomy of chromosome 2p", "partial deletion of chromosome 2p", "partial monosomy of the short arm of chromosome 2", "partial deletion of the short arm of chromosome 2", "partial deletion of the short arm of chromosome type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of the short arm of chromosome 2", "shortest_name_length": 33}
{"curie": "MONDO:0019764", "names": ["LTEC4", "LTEC IV", "laryngotracheoesophageal cleft type 4", "laryngo-tracheo-esophageal cleft type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laryngotracheoesophageal cleft type 4", "shortest_name_length": 5}
{"curie": "MONDO:0700031", "names": ["mosaic trisomy 18"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mosaic trisomy 18", "shortest_name_length": 17}
{"curie": "MONDO:0021404", "names": ["sphenoid sinus polyp", "Sphenoid Sinus Polyp", "Sphenoidal Sinus Polyp", "sphenoidal sinus polyp", "Sphenoidal sinus polyp", "Polyp of Sphenoid Sinus", "polyp of sphenoid sinus", "Polyp of sphenoidal sinus", "Polyp of Sphenoidal Sinus", "polyp of sphenoidal sinus", "Sphenoidal polyp of sinus", "Polyp of sinus, sphenoidal", "Polyp of the Sphenoid Sinus", "polyp of the sphenoid sinus", "Polyp of the Sphenoidal Sinus", "polyp of the sphenoidal sinus", "Polyp of sphenoidal sinus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyp of sphenoidal sinus", "shortest_name_length": 20}
{"curie": "UMLS:C5555677", "names": ["High Risk Breast Carcinoma", "High-Risk Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Risk Breast Carcinoma", "shortest_name_length": 26}
{"curie": "UMLS:C1266011", "names": ["Papillary urothelial carcinoma, non-invasive", "Non-Invasive Papillary Transitional Cell Carcinoma", "Papillary transitional cell carcinoma, non-invasive", "Papillary transitional cell carcinoma, non-invasive (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Papillary transitional cell carcinoma, non-invasive", "shortest_name_length": 44}
{"curie": "MONDO:0006123", "names": ["Heart Rhabdomyoma", "heart rhabdomyoma", "Cardiac Rhabdomyoma", "Cardiac rhabdomyoma", "cardiac rhabdomyoma", "Rhabdomyoma of Heart", "rhabdomyoma of heart", "rhabdomyoma of the heart", "Rhabdomyoma of the Heart", "cardiac rhabdomyoma (disease)", "rhabdomyoma of heart (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiac rhabdomyoma", "shortest_name_length": 17}
{"curie": "MONDO:0010523", "names": ["PDR", "XLPDR", "Partington disease", "Familial cutaneous amyloidosis", "X-linked cutaneous amyloidosis", "familial cutaneous amyloidosis", "amyloidosis, familial cutaneous", "Amyloidosis, Familial Cutaneous", "X-linked reticulate pigmentary disorder", "Pigmentary Disorder, Reticulate, with Systemic Manifestations", "pigmentary disorder, reticulate, with systemic manifestations", "PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS", "X-linked reticulate pigmentary disorder with systemic manifestations", "pigmentary disorder, reticulate, with systemic manifestations, X-linked", "PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS, X-LINKED", "X-linked reticulate pigmentary disorder with systemic manifestation syndrome", "X-linked reticulate pigmentary disorder with systemic manifestation syndrome (disorder)", "pigmentary disorder, reticulate, with systemic manifestations, X-linked, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked reticulate pigmentary disorder", "shortest_name_length": 3}
{"curie": "MONDO:0018310", "names": ["LCH", "Lch", "histiocytosis X", "Histiocytosis-X", "histiocytosis-x", "Histiocytosis X", "histiocytosis x", "histiocytosis; X", "X; histiocytosis", "HISTIOCYTOSIS X II", "Type 2 Histiocytosis", "Histiocytosis X, NOS", "Type 2 Histiocytoses", "Histiocytoses, Type 2", "Letterer-Siwe Disease", "Histiocytosis, Type 2", "Letterer Siwe Disease", "Letterer-Siwe disease", "Disease, Letterer-Siwe", "langerhans cell disease", "Chronic Histiocytosis X", "Langerhans cell disease", "Histiocytosis X syndrome", "Generalized Histiocytoses", "X; histiocytosis, chronic", "Generalized Histiocytosis", "histiocytosis; X, chronic", "generalized histiocytosis", "Histiocytoses, Generalized", "Histiocytosis, Generalized", "Schueller-Christian Disease", "Schueller Christian Disease", "Disease, Schueller-Christian", "cell histiocytosis langerhan", "Langerhans cell histiocytosis", "Langerhans-Cell Histiocytosis", "Langerhans-cell histiocytosis", "Langerhans Cell Histiocytosis", "LANGERHANS CELL HISTIOCYTOSIS", "Langerhans Cell Histiocytoses", "Letterer-siwe disease, spleen", "cell histiocytosis langerhans", "langerhans cell histiocytosis", "langerhan's cell histiocytosis", "langerhans cell granulomatosis", "Histiocytosis, Langerhans Cell", "Langerhans' cell histiocytosis", "cells histiocytosis langerhans", "Langerhans Cell Granulomatosis", "Cell Histiocytoses, Langerhans", "Histiocytoses, Langerhans Cell", "Langerhans-Cell Granulomatosis", "cell granulomatosis langerhans", "Langerhans Cell Granulomatoses", "Histiocytosis, Langerhans-Cell", "Langerhan's cell histiocytosis", "Cell Histiocytosis, Langerhans", "Langerhans cell granulomatosis", "Langerhans histiocytic syndrome", "Non Lipid Reticuloendotheliosis", "Non-Lipid Reticuloendotheliosis", "Granulomatosis, Langerhans-Cell", "Hand Schüller Christian Disease", "Letterer-Siwe disease of spleen", "Hand-Schüller-Christian Disease", "Cell Granulomatoses, Langerhans", "letterer-Siwe disease of spleen", "Granulomatosis, Langerhans Cell", "histiocytosis; Langerhans' cell", "Non-Lipid Reticuloendothelioses", "Cell Granulomatosis, Langerhans", "Granulomatoses, Langerhans Cell", "Langerhans' cell granulomatosis", "Langerhans' cell; histiocytosis", "Hand-Schuller-Christian disease", "Reticuloendothelioses, Non-Lipid", "Disease, Hand-Schüller-Christian", "Hand-Schüller-Christian Syndrome", "Hand Schüller Christian Syndrome", "Chronic idiopathic xanthomatosis", "Hand-Schueller-Christian Disease", "Hand Schueller Christian Disease", "Reticuloendotheliosis, Non-Lipid", "Syndrome, Hand-Schüller-Christian", "Langerhans-cell histiocytosis NOS", "Hand Schueller Christian Syndrome", "Disease, Hand-Schueller-Christian", "Hand-Schueller-Christian Syndrome", "EOSINOPHILIC GRANULOMA, MULTIFOCAL", "Langerhans Cell Histiocytosis, NOS", "Syndrome, Hand-Schueller-Christian", "Langerhans cell histiocytosis, NOS", "LCH - Langerhan's cell histiocytosis", "letterer-Siwe disease involving spleen", "Letterer-Siwe disease involving spleen", "Systemic Aleukemic Reticuloendothelioses", "Systemic Aleukemic Reticuloendotheliosis", "Langerhans cell histiocytosis (disorder)", "Differentiated progressive histiocytosis", "Reticuloendothelioses, Systemic Aleukemic", "Langerhans cell histiocytosis (diagnosis)", "Aleukemic Reticuloendothelioses, Systemic", "Reticuloendotheliosis, Systemic Aleukemic", "Aleukemic Reticuloendotheliosis, Systemic", "Letterer-Siwe disease of spleen (disorder)", "Letterer-Siwe disease of intrapelvic region", "Letterer-Siwe disease of spleen (diagnosis)", "Letterer-Siwe disease of head, face, or neck", "Letterer-Siwe disease of axilla or upper limbs", "Letterer-siwe disease, intrapelvic lymph nodes", "letterer-Siwe disease of intrapelvic lymph nodes", "Letterer-siwe disease, intrathoracic lymph nodes", "Letterer-Siwe disease of intrapelvic lymph nodes", "Letterer-siwe disease, intra-abdominal lymph nodes", "letterer-Siwe disease of intrathoracic lymph nodes", "Letterer-Siwe disease of intrathoracic lymph nodes", "letterer-Siwe disease of intra-abdominal lymph nodes", "Letterer-Siwe disease of intra-abdominal lymph nodes", "Letterer-siwe disease, lymph nodes of multiple sites", "Letterer-Siwe disease of lymph nodes of multiple sites", "Langerhans cell histiocytosis, Not otherwise specified", "Langerhans Cell Histiocytosis, Not Otherwise Specified", "letterer-Siwe disease of lymph nodes of multiple sites", "letterer-Siwe disease involving intrapelvic lymph nodes", "Letterer-Siwe disease involving intrapelvic lymph nodes", "Letterer-Siwe disease of inguinal region or lower limbs", "Letterer-Siwe disease of intrapelvic region (diagnosis)", "Langerhans' cell histiocytosis (morphologic abnormality)", "Letterer-Siwe disease of head, face, or neck (diagnosis)", "Letterer-Siwe disease involving intrathoracic lymph nodes", "letterer-Siwe disease involving intrathoracic lymph nodes", "Letterer-Siwe disease of axilla or upper limbs (diagnosis)", "Letterer-siwe disease, lymph nodes of head, face, and neck", "Letterer-Siwe disease of intrapelvic lymph nodes (disorder)", "letterer-Siwe disease involving intra-abdominal lymph nodes", "Letterer-Siwe disease of lymph nodes of head, face and neck", "letterer-Siwe disease of lymph nodes of head, face and neck", "Letterer-Siwe disease involving intra-abdominal lymph nodes", "Letterer-siwe disease, lymph nodes of axilla and upper limb", "Letterer-Siwe disease of lymph nodes of head, face, and neck", "Letterer-Siwe disease involving lymph nodes of multiple sites", "Letterer-Siwe disease of lymph nodes of axilla and upper limb", "letterer-Siwe disease involving lymph nodes of multiple sites", "letterer-Siwe disease of lymph nodes of axilla and upper limb", "Letterer-Siwe disease of intrathoracic lymph nodes (disorder)", "Letterer-Siwe disease of lymph nodes of head, face and/or neck", "letterer-Siwe disease of lymph nodes of head, face and/or neck", "Letterer-Siwe disease of intra-abdominal lymph nodes (disorder)", "letterer-Siwe disease of lymph nodes of axilla and/or upper limb", "Letterer-Siwe disease of lymph nodes of axilla and/or upper limb", "Letterer-Siwe disease of intra-abdominal lymph nodes (diagnosis)", "Letterer-Siwe disease of lymph nodes of multiple sites (disorder)", "letterer-Siwe disease involving lymph nodes of head, face and neck", "Letterer-Siwe disease of lymph nodes of multiple sites (diagnosis)", "Letterer-Siwe disease involving lymph nodes of head, face and neck", "Letterer-Siwe disease of inguinal region or lower limbs (diagnosis)", "Letterer-Siwe disease involving lymph nodes of head, face, and neck", "letterer-Siwe disease involving lymph nodes of head, face, and neck", "letterer-Siwe disease involving lymph nodes of axilla and upper limb", "Letterer-Siwe disease involving lymph nodes of axilla and upper limb", "Letterer-siwe disease, lymph nodes of inguinal region and lower limb", "Letterer-Siwe disease of lymph nodes of inguinal region and lower limb", "letterer-Siwe disease of lymph nodes of inguinal region and lower limb", "Letterer-Siwe disease of lymph nodes of inguinal region amd/or lower limb", "letterer-Siwe disease of lymph nodes of inguinal region amd/or lower limb", "Letterer-Siwe disease of lymph nodes of inguinal region and/or lower limb", "letterer-Siwe disease of lymph nodes of inguinal region and/or lower limb", "letterer-Siwe disease involving lymph nodes of inguinal region and lower limb", "Letterer-Siwe disease involving lymph nodes of inguinal region and lower limb"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Langerhans cell histiocytosis", "shortest_name_length": 3}
{"curie": "MONDO:0007941", "names": ["MALOCCLUSION DUE TO PROTUBERANT UPPER FRONT TEETH", "malocclusion due to protuberant upper front teeth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malocclusion due to protuberant upper front teeth", "shortest_name_length": 49}
{"curie": "MONDO:0006912", "names": ["pneumatosis coli", "Pneumatosis coli", "INTESTINE, GAS CYSTS", "EMPHYSEMA, INTESTINAL", "pneumatosis cystoides coli", "Pneumatosis coli (disorder)", "Pneumatosis intestinalis cystica", "pneumatosis cystoides intestinalis", "Pneumatosis Cystoides Intestinalis", "PNEUMATOSIS CYSTOIDES INTESTINALIS", "Pneumatosis cystoides intestinalis", "cystoides intestinalis pneumatosis", "Cystoides Intestinalis, Pneumatosis", "cystoides intestinalis; pneumatosis", "Intestinalis, Pneumatosis Cystoides", "pneumatosis; cystoides intestinalis", "pneumatosis cystoides coli (diagnosis)", "PCI - Pneumatosis cystoides intestinalis", "Pneumatosis cystoides intestinalis (disorder)", "pneumatosis cystoides intestinalis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pneumatosis cystoides intestinalis", "shortest_name_length": 16}
{"curie": "MONDO:0009583", "names": ["Ohdo syndrome", "OHDO SYNDROME", "BMRS, Ohdo type", "Ohdo Madokoro Sonoda syndrome", "Ohdo-Madokoro-Sonoda syndrome", "Ohdo blepharophimosis syndrome", "Ohdo Blepharophimosis syndrome", "OHDO BLEPHAROPHIMOSIS SYNDROME", "Blepharophimosis syndrome Ohdo type", "blepharophimosis syndrome, Ohdo type", "Blepharophimosis syndrome, Ohdo type", "Blepharophimosis-intellectual disability syndrome, Ohdo type", "blepharophimosis - intellectual disability syndrome, Ohdo type", "Mental retardation, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth", "mental retardation, congenital heart disease, blepharophimosis, blepharoptosis, and hypoplastic teeth", "mental retardation-congenital heart disease-blepharophimosis-blepharoptosis-hypoplastic teeth disease", "Mental Retardation, Congenital Heart Disease, Blepharophimosis, Blepharoptosis, And Hypoplastic Teeth", "MENTAL RETARDATION, CONGENITAL HEART DISEASE, BLEPHAROPHIMOSIS, BLEPHAROPTOSIS, AND HYPOPLASTIC TEETH", "Intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth", "intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis, and hypoplastic teeth", "Intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth (disorder)", "intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis, and hypoplastic teeth (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blepharophimosis - intellectual disability syndrome, Ohdo type", "shortest_name_length": 13}
{"curie": "UMLS:C0563247", "names": ["blood blister", "Blood blister", "blister blood", "blisters blood", "Blood blister (disorder)", "Blood blister (diagnosis)", "superficial injury blister blood", "Blood blister (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Blood blister", "shortest_name_length": 13}
{"curie": "MONDO:0032622", "names": ["MC1DN17", "nuclear type mitochondrial complex I deficiency 17", "mitochondrial complex 1 deficiency, nuclear type 17", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 17"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 17", "shortest_name_length": 7}
{"curie": "UMLS:C1608397", "names": ["Device occlusion", "Gastrostomy-jejunostomy tube obstruction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Device occlusion", "shortest_name_length": 16}
{"curie": "UMLS:C4528701", "names": ["Tumor Stage (Pathological)", "Cutaneous Melanoma by AJCC v8 Pathologic Stage", "Melanoma of the Skin by AJCC v8 Pathologic Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous Melanoma by AJCC v8 Pathologic Stage", "shortest_name_length": 26}
{"curie": "MONDO:0009726", "names": ["NNS", "NKJO", "ALDD", "PRAAS", "JMP syndrome", "JMP SYNDROME", "ALDD syndrome", "Nakajo syndrome", "CANDLE syndrome", "Nakajo-Nishimura syndrome", "NAKAJO-NISHIMURA SYNDROME", "Nakajo Nishimura syndrome", "amyotrophy fat tissue anomaly", "Proteasome disability syndrome", "proteasome disability syndrome", "Nodular erythema digital changes", "nodular erythema digital changes", "Nodular Erythema With Digital Changes", "amyotrophy-fat tissue anomaly syndrome", "proteasome-associated autoinflammatory syndrome", "Proteasome-associated autoinflammatory syndrome", "proteosome-associated autoinflammatory syndrome", "autoinflammation-lipodystrophy-dermatosis syndrome", "Autoinflammation-lipodystrophy-dermatosis syndrome", "secondary hypertrophic osteoperiostosis with pernio", "Japanese autoinflammatory syndrome with lipodystrophy", "Autoinflammation, lipodystrophy and dermatosis syndrome", "autoinflammation, lipodystrophy, and dermatosis syndrome", "AUTOINFLAMMATION, LIPODYSTROPHY, AND DERMATOSIS SYNDROME", "Autoinflammation, lipodystrophy and dermatosis syndrome (disorder)", "chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature", "chronic atypical neutrophilic dermatosis-lipodystrophy-elevated temperature syndrome", "Joint contractures - muscle atrophy - microcytic anemia - panniculitis-induced lipodystrophy", "chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature syndrome", "JOINT CONTRACTURES, MUSCULAR ATROPHY, MICROCYTIC ANEMIA, AND PANNICULITIS-INDUCED LIPODYSTROPHY", "Joint contractures, muscular atrophy, microcytic Anemia, and panniculitis-induced lipodystrophy", "joint contractures, muscular atrophy, microcytic anemia, and panniculitis-induced lipodystrophy", "Joint contractures-muscular atrophy-microcytic anemia-panniculitis-associated lipodystrophy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "proteosome-associated autoinflammatory syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0023079", "names": ["epidermal nevus vitamin D resistant rickets"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermal nevus vitamin D resistant rickets", "shortest_name_length": 43}
{"curie": "MONDO:0013893", "names": ["MS5", "susceptibility to multiple sclerosis 5", "multiple sclerosis, susceptibility to, 5", "MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO, 5", "multiple sclerosis, susceptibility to, type 5", "TNFRSF1A multiple sclerosis, susceptibility to", "multiple sclerosis, susceptibility to caused by mutation in TNFRSF1A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple sclerosis, susceptibility to, 5", "shortest_name_length": 3}
{"curie": "MONDO:0800025", "names": ["TBHS", "TBHS1", "Teebi syndrome", "OGS2, FORMERLY", "BBBG2, FORMERLY", "GBBB2, FORMERLY", "Opitz G Syndrome", "Opitz BBB Syndrome", "Opitz BBBG syndrome", "Opitz-Frias syndrome", "Opitz G-BBB Syndrome", "Opitz G/BBB Syndrome", "Opitz-G/BBB syndrome", "Opitz BBB-G Syndrome", "Hypertelorism Teebi type", "Opitz-G syndrome, type 2", "Hypertelorism, Teebi type", "HYPERTELORISM, TEEBI TYPE", "hypertelorism, Teebi type", "Opitz-G Syndrome, Type II", "Opitz GBBB syndrome type II", "Opitz GBBB Syndrome, Type II", "Teebi hypertelorism syndrome", "TEEBI HYPERTELORISM SYNDROME", "OPITZ-FRIAS SYNDROME, FORMERLY", "Teebi hypertelorism syndrome 1", "Teebi hypertelorism syndrome-1", "Hypospadias-Dysphagia Syndrome", "TEEBI HYPERTELORISM SYNDROME 1", "Hypospadias-dysphagia, syndrome", "Hypertelorism-Hypospadias Sydrome", "BRACHYCEPHALOFRONTONASAL DYSPLASIA", "Hypertelorism hypospadias syndrome", "Brachycephalofrontonasal dysplasia", "Hypertelorism Teebi type (disorder)", "OPITZ-G SYNDROME, TYPE II, FORMERLY", "OPITZ BBB SYNDROME, TYPE II, FORMERLY", "OPITZ GBBB SYNDROME, TYPE II, FORMERLY", "SPECC1L-related hypertelorism syndrome", "Craniofrontonasal dysplasia Teebi type", "OPITZ BBBG SYNDROME, TYPE II, FORMERLY", "Opitz GBBB Syndrome, Autosomal Dominant", "craniofrontonasal dysplasia, Teebi type", "Autosomal Dominant Opitz Syndrome (ADOS)", "Telecanthus with associated abnormalities", "Opitz Oculogenitolaryngeal Syndrome, Type II", "HYPERTELORISM-HYPOSPADIAS SYNDROME, FORMERLY", "CHROMOSOME 22q11.2 DELETION SYNDROME, OPITZ PHENOTYPE", "Chromosome 22q11.2 Deletion Syndrome, Opitz Phenotype", "OPITZ OCULOGENITOLARYNGEAL SYNDROME, TYPE II, FORMERLY", "Hypertelorism with esophageal abnormality and hypospadias", "Hypertelorism with Esophageal Abnormalities and Hypospadias", "HYPERTELORISM WITH ESOPHAGEAL ABNORMALITY AND HYPOSPADIAS, FORMERLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Teebi hypertelorism syndrome 1", "shortest_name_length": 4}
{"curie": "MONDO:0010980", "names": ["Dincsoy syndrome", "DINCSOY SYNDROME", "Dincsoy-Salih-Patel syndrome", "Dincsoy Salih Patel syndrome", "Midline malformations, multiple, with limb abnormalities and hypopituitarism", "MIDLINE MALFORMATIONS, MULTIPLE, WITH LIMB ABNORMALITIES AND HYPOPITUITARISM", "midline malformations, multiple, with limb abnormalities and hypopituitarism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "midline malformations, multiple, with limb abnormalities and hypopituitarism", "shortest_name_length": 16}
{"curie": "MONDO:0007399", "names": ["CRS", "CRS1", "craniostenosis", "craniosynostosis 1", "CRANIOSYNOSTOSIS 1", "Type 1 Craniosynostosis", "craniosynostosis type 1", "Type 1 Craniosynostoses", "Craniosynostosis, Type 1", "1 Craniosynostosis, Type", "1 Craniosynostoses, Type", "Craniosynostoses, Type 1", "TWIST1-related craniosynostosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "TWIST1-related craniosynostosis", "shortest_name_length": 3}
{"curie": "MONDO:0007924", "names": ["BZS", "BRRS", "RMSS", "Bannayan Syndrome", "bannayan syndrome", "Cowden syndrome 1", "Bannayan syndrome", "riley-smith syndrome", "Riley-Smith syndrome", "Riley Smith Syndrome", "RILEY-SMITH syndrome", "Riley-Smith Syndrome", "riley smith syndrome", "Riley Smith syndrome", "Bannayan-Zonana Syndrome", "Ruvalcaba-Myhre Syndrome", "ruvalcaba-myhre syndrome", "Bannayan Zonana Syndrome", "Bannayan-Zonana syndrome", "bannayan zonana syndrome", "bannayan-zonana syndrome", "Ruvalcaba-Myhre syndrome", "Myhre-Riley-Smith syndrome", "Myhre Riley Smith Syndrome", "Myhre-Riley-Smith Syndrome", "Bannayan syndrome (disorder)", "Ruvalcaba Myhre Smith syndrome", "Ruvalcaba-Myhre-Smith syndrome", "Ruvalcaba-MYHRE-SMITH syndrome", "Bannayan-Zonana syndrome (BZS)", "Ruvalcaba-Myhre-Smith Syndrome", "Ruvalcaba Myhre Smith Syndrome", "Ruvalcaba -Myhre-Smith syndrome", "macrocephaly-hamartomas syndrome", "Bannayan-Ruvalcaba-Riley Syndrome", "Bannayan Riley Ruvalcaba Syndrome", "Bannayan-Riley-Ruvalcaba syndrome", "Bannayan-Riley-Ruvalcaba Syndrome", "Ruvalcaba-Myhre-Smith syndrome (RMSS)", "Bannayan-Riley-Ruvalcaba syndrome (BRRS)", "Ruvalcaba-Myhre-Smith syndrome (diagnosis)", "macrocephaly multiple lipomas and hemangiomata", "macrocephaly, multiple lipomas, and hemangiomata", "Macrocephaly, Multiple Lipomas, and Hemangiomata", "Macrocephaly with Multiple Lipomas and Hemangiomas", "Macrocephaly with multiple lipomas and hemangiomas", "macrocephaly with multiple lipomas and hemangiomas", "Macrocephaly with multiple lipomas and haemangiomas", "macrocephaly-multiple lipomas-hemangiomata syndrome", "Hemangiomata with macrocephaly and pseudopapilledema", "Haemangiomata with macrocephaly and pseudopapilloedema", "macrocephaly pseudopapilledema and multiple hemangiomas", "Macrocephaly, Pseudopapilledema, and Multiple Hemangiomas", "macrocephaly, pseudopapilledema, and multiple hemangiomata", "Macrocephaly, Pseudopapilledema, and Multiple Hemangiomata", "macrocephaly-pseudoepithelioma-multiple hemangiomas syndrome", "Macrocephaly, pseudopapilledema, multiple hemangiomata syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bannayan-Riley-Ruvalcaba syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C2981708", "names": ["IIIA", "Stage IIIA Uveal Melanoma", "Stage IIIA Uveal Melanoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Uveal Melanoma AJCC v7", "shortest_name_length": 4}
{"curie": "MONDO:0043510", "names": ["BRAIN DAMAGE", "Brain damage", "Brain Injury", "damage brain", "brain trauma", "injury brain", "brain damage", "brain injury", "Brain Damage", "Brain injury", "damage; brain", "Damage, brain", "brain Traumas", "brain; injury", "brain damages", "Injury, Brain", "injury; brain", "brain; damage", "Brain Injuries", "brain injuries", "Injuries, Brain", "injury of brain", "cerebral injury", "cerebral damage", "Cerebral damage", "Injury;cerebral", "injury; cerebral", "cerebral; injury", "Brain injury NOS", "Brain damage, NOS", "brain tissue injury", "brain injury tissue", "Brain tissue injury", "Intracerebral injury", "acquired brain injury", "Acquired brain injury", "Injury;brain;acquired", "disorder brain injury", "brain disorders injury", "brain injury (diagnosis)", "brain lesion (from injury)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brain injury", "shortest_name_length": 12}
{"curie": "MONDO:0020167", "names": ["malposition of external canthus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malposition of external canthus", "shortest_name_length": 31}
{"curie": "UMLS:C4331330", "names": ["Stage III Oropharyngeal (p16-Negative) Throat Cancer", "Stage III Oropharyngeal (p16-Negative) Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Oropharyngeal (p16-Negative) Carcinoma AJCC v8", "shortest_name_length": 52}
{"curie": "UMLS:C4525725", "names": ["Nuclear Cataract Grade 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nuclear Cataract Grade 3", "shortest_name_length": 24}
{"curie": "UMLS:C0264010", "names": ["Hepatic osteodystrophy", "Hepatic osteodystrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatic osteodystrophy", "shortest_name_length": 22}
{"curie": "UMLS:C4525123", "names": ["Stage IIB Colon Cancer", "Stage IIB Colon Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Colon Cancer AJCC v8", "shortest_name_length": 22}
{"curie": "MONDO:0032830", "names": ["SNIBFIS", "SNIJDERS BLOK-FISHER SYNDROME", "snijders blok-fisher syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "snijders blok-fisher syndrome", "shortest_name_length": 7}
{"curie": "MONDO:0009187", "names": ["CEC", "Epilepsy occipital calcifications", "epilepsy occipital calcifications", "epilepsy with bilateral occipital calcifications", "Epilepsy with bilateral occipital calcifications", "Bilateral occipital calcifications with epilepsy", "EPILEPSY WITH BILATERAL OCCIPITAL CALCIFICATIONS", "bilateral occipital calcifications with epilepsy", "celiac disease epilepsy occipital calcifications", "celiac disease-epilepsy-cerebral calcification syndrome", "celiac disease, epilepsy, and cerebral calcification syndrome", "familial unilateral and bilateral occipital calcifications and epilepsy", "Familial unilateral and bilateral occipital calcifications and epilepsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "celiac disease-epilepsy-cerebral calcification syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0019819", "names": ["Double orifice mitral valve", "double-orifice mitral valve", "Double-orifice mitral valve", "Mitral valve, double orifice", "Double orifice of mitral valve", "Double orifice of mitral valve (disorder)", "Double orifice of mitral valve (diagnosis)", "mitral valve leaflet abnormality double orifice"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "double-orifice mitral valve", "shortest_name_length": 27}
{"curie": "MONDO:0013984", "names": ["DFNB84B", "autosomal recessive deafness 84B", "deafness, autosomal recessive 84B", "DEAFNESS, AUTOSOMAL RECESSIVE 84B", "deafness, autosomal recessive 84b", "deafness, autosomal recessive type 84B", "autosomal recessive nonsyndromic deafness 84B", "OTOGL autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 84B", "autosomal recessive nonsyndromic deafness type 84B", "autosomal recessive nonsyndromic deafness caused by mutation in OTOGL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 84B", "shortest_name_length": 7}
{"curie": "MONDO:0024355", "names": ["RTI", "rti", "INFECTION RESPIRATORY", "Respiratory infection", "Infection respiratory", "RESPIRATORY INFECTION", "Infection;respiratory", "respiratory infection", "Respiratory Infections", "Respiratory infections", "respiratory infections", "infections, respiratory", "Infections, Respiratory", "Respiratory Tract Infection", "respiratory tract infection", "Respiratory tract infection", "RESPIRATORY TRACT INFECTION", "respiratory tract; infection", "Respiratory System Infection", "respiratory infection, upper", "infection, respiratory tract", "Respiratory Tract Infections", "Respiratory tract infections", "upper respiratory infections", "Infection, Respiratory Tract", "infection; respiratory tract", "respiratory tract infections", "Respiratory System Infections", "Infections, Respiratory Tract", "infections, respiratory tract", "infections, upper respiratory", "Infection, Respiratory System", "Respiratory tract infection NOS", "respiratory tract infection (RTI)", "RTI - Respiratory tract infection", "upper respiratory tract infections", "infections, upper respiratory tract", "respiratory tract infectious disorder", "Respiratory tract infection (disorder)", "respiratory tract infection (diagnosis)", "Unspecified respiratory tract infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "respiratory tract infectious disorder", "shortest_name_length": 3}
{"curie": "UMLS:C1333133", "names": ["Common Variant Anaplastic Large Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Common Variant Anaplastic Large Cell Lymphoma", "shortest_name_length": 45}
{"curie": "MONDO:0002947", "names": ["Melanotic adamantinoma of skin", "melanotic adamantinoma of skin", "Melanotic ameloblastoma of skin", "adamantinoid basal cell carcinoma", "Adamantinoid Basal Cell Carcinoma", "Adamantinoid basal cell epithelioma", "Basal cell carcinoma - adamantinoid", "basal cell carcinoma - adamantinoid", "adamantinoid basal cell epithelioma", "skin adamantinoid basal cell carcinoma", "Skin Adamantinoid Basal Cell Carcinoma", "Skin Adamantinoid Basal Cell Epithelioma", "skin adamantinoid basal cell epithelioma", "Basal cell carcinoma - adamantinoid (disorder)", "Basal cell carcinoma - adamantinoid (diagnosis)", "malignant neoplasm carcinoma basal cell adamantinoid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adamantinoid basal cell epithelioma", "shortest_name_length": 30}
{"curie": "MONDO:0009943", "names": ["PYL", "Pyl", "pyle", "PYLE", "Pyle", "pyles", "PYLE DISEASE", "pyle disease", "Pyle disease", "Pyle's disease", "Pyle's syndrome", "Pyle-Cohn syndrome", "Edwin Pyle disease", "Metaphyseal dysplasia", "Bakwin-Krida syndrome", "metaphyseal dysplasia", "dysplasia; metaphyseal", "metaphyseal; dysplasia", "Pyle metaphyseal dysplasia", "metaphyseal dysplasia Pyle type", "metaphyseal dysplasia, Pyle type", "Metaphyseal dysplasia, Pyle type", "METAPHYSEAL DYSPLASIA, PYLE TYPE", "metaphyseal dysplasia (diagnosis)", "Pyle's metaphyseal dysplasia syndrome", "Pyle metaphyseal dysplasia (disorder)", "chondrodysplasia calcificans metaphysealis", "osteochondrodysplasia metaphyseal dysplasia", "Metaphyseal dysplasia with little involvement of the cranial bones"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pyle disease", "shortest_name_length": 3}
{"curie": "UMLS:C0948048", "names": ["Malignant neoplasm progression"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant neoplasm progression", "shortest_name_length": 30}
{"curie": "UMLS:C3272759", "names": ["Brain Development Abnormality", "Brain Developmental Abnormality"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brain Development Abnormality", "shortest_name_length": 29}
{"curie": "MONDO:0600023", "names": ["IIM", "IMM", "idiopathic myositis", "Idiopathic Inflammatory Myopathy", "Idiopathic Inflammatory Myositis", "inflammatory myopathy idiopathic", "Idiopathic inflammatory myositis", "Idiopathic inflammatory myopathy", "idiopathic inflammatory myopathy", "Inflammatory Myopathy, Idiopathic", "Myopathy, Idiopathic Inflammatory", "idiopathic inflammatory myopathies", "Idiopathic Inflammatory Myopathies", "Inflammatory Myopathies, Idiopathic", "Myopathies, Idiopathic Inflammatory", "Idiopathic inflammatory myopathy (disorder)", "Idiopathic inflammatory myopathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic inflammatory myopathy", "shortest_name_length": 3}
{"curie": "MONDO:0016070", "names": ["HGF", "GINGF", "Gingival fibroma", "Gingival Fibromatosis", "Fibromatosis Gingivae", "fibromatosis; gingiva", "Gingival Fibromatoses", "gingival fibromatosis", "Gingival fibromatosis", "gingiva; fibromatosis", "Fibromatoses, Gingival", "Fibromatosis, Gingival", "Gingival fibrous nodules", "hereditary gingival hyperplasia", "Idiopathic gingival hyperplasia", "Hereditary gingival hyperplasia", "Hereditary gingival fibromatosis", "hereditary gingival fibromatosis", "Gingival fibromatosis (disorder)", "gingival fibromatosis (diagnosis)", "Fibromatosis, Gingival, Hereditary", "FIBROMATOSIS, GINGIVAL, HEREDITARY", "autosomal dominant gingival hyperplasia", "Autosomal dominant gingival hyperplasia", "autosomal dominant gingival fibromatosis", "Autosomal dominant gingival fibromatosis", "Hereditary fibrous enlargement of gingiva", "Hereditary gingival fibromatosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary gingival fibromatosis", "shortest_name_length": 3}
{"curie": "UMLS:C4682696", "names": ["Stage IIB Penile Cancer", "stage IIB penile cancer", "Stage IIB Penile Cancer AJCC v8", "stage IIB penile cancer AJCC v8", "stage IIB penile squamous cell carcinoma AJCC v8", "Stage IIB Penile Squamous Cell Carcinoma AJCC v8", "stage IIB squamous cell carcinoma of the penis AJCC v8", "Stage IIB Squamous Cell Carcinoma of the Penis AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Penile Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "MONDO:0023073", "names": ["cystitis eosinophilic", "CYSTITIS EOSINOPHILIC", "Eosinophilic cystitis", "eosinophilic cystitis", "cystitis; eosinophilic", "eosinophilic; cystitis", "eosinophilic cryptitis", "Eosinophilic cystitis (disorder)", "Eosinophilic bladder infiltration", "Eosinophilic cystitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eosinophilic cryptitis", "shortest_name_length": 21}
{"curie": "UMLS:C2931205", "names": ["Usher syndrome type 1A", "Usher Syndrome, Type 1", "Usher Syndrome, Type I", "Usher syndrome, type 1A", "Usher Syndrome, Type 1A", "Usher syndrome type 1A (diagnosis)", "Usher Syndrome, Type I, French Variety", "Retinitis Pigmentosa And Congenital Deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Usher syndrome, type 1A", "shortest_name_length": 22}
{"curie": "MONDO:0001006", "names": ["Glaucomatous optic atrophy", "glaucomatous optic atrophy", "Optic disc glaucomatous atrophy", "Glaucomatous optic disc atrophy", "Glaucomatous optic disc cupping", "Glaucomatous cupping of optic disc", "glaucomatous atrophy of optic disc", "Glaucomatous atrophy of optic disc", "glaucomatous optic atrophy (diagnosis)", "Glaucomatous atrophy [cupping] of optic disc", "glaucomatous atrophy [cupping] of optic disc", "Glaucomatous atrophy of optic disc (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glaucomatous atrophy of optic disc", "shortest_name_length": 26}
{"curie": "MONDO:0004950", "names": ["Stomach Cancer", "stomach cancer", "gastric cancer", "Gastric cancer", "Gastric Cancer", "Stomach cancer", "CARCINOMA STOMACH", "gastric carcinoma", "CARCINOMA GASTRIC", "STOMACH CARCINOMA", "Cancer of Stomach", "carcinoma gastric", "Carcinoma stomach", "stomach carcinoma", "Stomach Carcinoma", "Carcinoma;stomach", "carcinoma stomach", "Gastric Carcinoma", "Carcinoma gastric", "Gastric carcinoma", "cancer of stomach", "GASTRIC CARCINOMA", "Stomach carcinoma", "carcinomas gastric", "STOMACH, CARCINOMA", "carcinomas stomach", "gastric cancer, NOS", "Gastric cancer, NOS", "Ca fundus - stomach", "carcinoma of stomach", "Carcinoma of stomach", "CARCINOMA OF STOMACH", "Carcinoma of Stomach", "Cancer of the Stomach", "cancer of the stomach", "gastric fundus cancer", "Gastric (Stomach) Cancer", "gastric (stomach) cancer", "carcinoma of the stomach", "fundus of stomach cancer", "Carcinoma of the Stomach", "GASTRIC CANCER, CARCINOMA", "cancer of fundus of stomach", "Carcinoma of stomach (disorder)", "carcinoma of stomach (diagnosis)", "malignant tumor of fundus of stomach", "malignant fundus of stomach neoplasm", "Malignant tumor of fundus of stomach", "malignant neoplasm of gastric fundus", "Malignant tumour of fundus of stomach", "malignant neoplasm of fundus of stomach", "Malignant neoplasm of fundus of stomach", "Malignant tumor of fundus of stomach (disorder)", "malignant neoplasm of fundus of stomach (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric carcinoma", "shortest_name_length": 14}
{"curie": "MONDO:0020699", "names": ["biotin metabolic disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "biotin metabolic disease", "shortest_name_length": 24}
{"curie": "UMLS:C4086365", "names": ["Gonadal Thrombosis", "Gonadal Vein Thrombosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gonadal Thrombosis", "shortest_name_length": 18}
{"curie": "UMLS:C5670410", "names": ["Unresectable High Grade Ovarian Serous Adenocarcinoma", "Unresectable Ovarian High Grade Serous Adenocarcinoma", "Unresectable High-Grade Ovarian Serous Adenocarcinoma", "Unresectable Ovarian High-Grade Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Ovarian High Grade Serous Adenocarcinoma", "shortest_name_length": 53}
{"curie": "MONDO:0018995", "names": ["CMT4", "AR-CMT1", "Charcot-Marie-Tooth disease type 4", "Charcot-Marie-Tooth disease Type 4", "hereditary motor and sensory neuropathy", "Charcot-Marie-Tooth disease type 4 (disorder)", "Charcot-Marie-Tooth disease Type 4 (diagnosis)", "Autosomal recessive demyelinating Charcot-Marie-Tooth", "autosomal recessive demyelinating Charcot-Marie-Tooth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 4", "shortest_name_length": 4}
{"curie": "MONDO:0007647", "names": ["GASTRIC VOLVULUS, INTRATHORACIC", "gastric volvulus, intrathoracic", "Gastric Volvulus, Intrathoracic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric volvulus, intrathoracic", "shortest_name_length": 31}
{"curie": "MONDO:0001094", "names": ["open-angle glaucoma residual stage", "residual stage open-angle glaucoma", "Open-angle glaucoma residual stage", "residual stage of open angle glaucoma", "Residual stage of open angle glaucoma", "residual stage of open-angle glaucoma", "Residual stage of open-angle glaucoma", "residual stage of open-angle glaucoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "residual stage of open angle glaucoma", "shortest_name_length": 34}
{"curie": "MONDO:0024323", "names": ["glomangiomyoma", "Glomangiomyoma", "[M] Glomangiomyoma", "Glomangiomyoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glomangiomyoma", "shortest_name_length": 14}
{"curie": "UMLS:C1710109", "names": ["Small Intestinal Mucinous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Intestinal Mucinous Adenocarcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0015298", "names": ["pellucid marginal degeneration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pellucid marginal degeneration", "shortest_name_length": 30}
{"curie": "MONDO:0008488", "names": ["Steinfeld Syndrome", "STEINFELD SYNDROME", "STEINFELD syndrome", "Steinfeld syndrome", "Steinfeld syndrome (disorder)", "holoprosencephaly radial heart renal anomalies", "Holoprosencephaly-radial heart renal anomalies syndrome", "holoprosencephaly-radial heart renal anomalies syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "holoprosencephaly-radial heart renal anomalies syndrome", "shortest_name_length": 18}
{"curie": "MONDO:0003722", "names": ["Internal Auditory Canal Meningioma", "internal auditory canal meningioma", "Meningioma of Internal Auditory Canal", "meningioma of internal auditory canal", "meningioma of the internal auditory canal", "Meningioma of the Internal Auditory Canal", "meningioma of the Internal Auditory canal", "internal acoustic meatus meningioma (disease)", "meningioma (disease) of internal acoustic meatus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "internal auditory canal meningioma", "shortest_name_length": 34}
{"curie": "UMLS:C3641119", "names": ["Acquired Phrenic Nerve Palsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired Phrenic Nerve Palsy", "shortest_name_length": 28}
{"curie": "MONDO:0017565", "names": ["macrodactyly of hand, bilateral", "macrodactyly of fingers, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macrodactyly of fingers, bilateral", "shortest_name_length": 31}
{"curie": "UMLS:C0740253", "names": ["fistula; empyema", "empyema; fistula", "pyothorax; fistula", "fistula; pyothorax", "Empyema with fistula", "Empyema with Fistula", "Pyothorax with fistula", "Empyema with fistula, NOS", "Empyema with pleural fistula", "Pleural empyema with fistula", "Empyema with thoracic fistula", "empyema of pleura with fistula", "Pleural empyema with fistula (disorder)", "empyema of pleura with fistula (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Empyema with fistula", "shortest_name_length": 16}
{"curie": "UMLS:C1610054", "names": ["graft-versus-host disease of liver", "Graft versus host disease of liver", "Graft versus host disease in liver", "graft-versus-host disease (GVHD) of liver", "Graft versus host disease of liver (disorder)", "graft-versus-host disease of liver (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Graft versus host disease in liver", "shortest_name_length": 34}
{"curie": "UMLS:C0278853", "names": ["Stage II Thyroid Follicular Cancer", "stage II follicular thyroid cancer", "follicular thyroid cancer, stage II", "thyroid cancer, stage II follicular", "Stage II Thyroid Follicular Carcinoma", "carcinoma, follicular, thyroid, stage II", "Stage II Follicular Carcinoma of Thyroid", "Stage II Thyroid Gland Follicular Cancer", "Stage II Thyroid Gland Follicular Carcinoma", "Stage II Follicular Thyroid Gland Carcinoma", "Stage II Follicular Carcinoma of the Thyroid", "follicular carcinoma of the thyroid, stage II", "Stage II Follicular Carcinoma of Thyroid Gland", "Stage II Follicular Carcinoma of the Thyroid Gland", "Stage II Thyroid Gland Follicular Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Thyroid Gland Follicular Carcinoma AJCC v7", "shortest_name_length": 34}
{"curie": "MONDO:0021381", "names": ["Pericardial Tumor", "pericardial tumor", "pericardium tumor", "pericardium neoplasm", "Tumor of Pericardium", "Pericardial neoplasm", "tumor of pericardium", "Tumor of pericardium", "pericardial neoplasm", "Pericardial Neoplasm", "Tumour of pericardium", "Neoplasm of pericardium", "Neoplasm of Pericardium", "neoplasm of pericardium", "tumor of the pericardium", "Tumor of the Pericardium", "neoplasm of the pericardium", "Neoplasm of the Pericardium", "pericardial tumor (diagnosis)", "pericardium neoplasm (disease)", "Neoplasm of pericardium (disorder)", "neoplasm of pericardium (diagnosis)", "Neoplasm of uncertain behavior of pericardium", "Neoplasm of uncertain behaviour of pericardium", "cardiac neoplasm uncertain behavior of pericardium", "Neoplasm of uncertain behavior of pericardium (disorder)", "Neoplasm of uncertain behavior of pericardium (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplasm of pericardium", "shortest_name_length": 17}
{"curie": "MONDO:0009017", "names": ["corneal degeneration, band-shaped spheroid", "CORNEAL DEGENERATION, BAND-SHAPED SPHEROID"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal degeneration, band-shaped spheroid", "shortest_name_length": 42}
{"curie": "UMLS:C2825180", "names": ["Proximal Left Anterior Descending Coronary Artery Stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Proximal Left Anterior Descending Coronary Artery Stenosis", "shortest_name_length": 58}
{"curie": "UMLS:C5420179", "names": ["Neuroendocrine Carcinoma, Excluding Head and Neck"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neuroendocrine Carcinoma, Excluding Head and Neck", "shortest_name_length": 49}
{"curie": "UMLS:C0940282", "names": ["Gastric polyp bleeding", "Gastric polyp hemorrhage", "Gastric polyp haemorrhage", "Bleeding of gastric polyp", "Gastrointestinal polyp bleeding", "Gastrointestinal polyp hemorrhage", "Gastrointestinal polyp haemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal polyp hemorrhage", "shortest_name_length": 22}
{"curie": "MONDO:0042605", "names": ["DAZ", "deleted in azoospermia", "Y chromosome infertility", "Y chromosome microdeletions", "male sterility due to Y-chromosome deletions", "Y chromosome infertility due to DAZ1 deletion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Y chromosome infertility due to DAZ1 deletion", "shortest_name_length": 3}
{"curie": "UMLS:C4683619", "names": ["Chronic Lymphocytic Leukemia- Modified Rai Staging System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic Lymphocytic Leukemia- Modified Rai Staging System", "shortest_name_length": 57}
{"curie": "MONDO:0033614", "names": ["SPG83", "hereditary spastic paraplegia 83", "spastic paraplegia 83 autosomal recessive", "SPASTIC PARAPLEGIA 83, AUTOSOMAL RECESSIVE", "spastic paraplegia 83, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic paraplegia 83, autosomal recessive", "shortest_name_length": 5}
{"curie": "MONDO:0006156", "names": ["colon SSP", "Colon SSA", "colon SSA", "Colon SSP", "colon SSA/P", "Colon SSA/P", "Colon Sessile Serrated Polyp", "Sessile serrated colon polyp", "colon sessile serrated polyp", "colon sessile serrated adenoma", "Colon Sessile Serrated Adenoma", "Sessile serrated polyp of colon", "Colon Serrated Lesions and Polyps", "Sessile serrated adenoma of colon", "colon sessile serrated adenoma/polyp", "Colon Sessile Serrated Adenoma/Polyp", "Sessile serrated polyp of colon (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colon sessile serrated adenoma/polyp", "shortest_name_length": 9}
{"curie": "UMLS:C0677948", "names": ["Dukes B colorectal cancer", "Colorectal cancer stage II", "Stage II Colorectal Cancer", "stage II colorectal cancer", "Dukes B Colorectal Carcinoma", "Stage II Colorectal Cancer AJCC v6", "Colorectal Cancer, Stage II AJCC v6", "Stage II Colorectal Carcinoma AJCC v6", "Colorectal Carcinoma Stage II AJCC v6", "Stage II Colorectal (Colon or Rectal) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Colorectal Cancer", "shortest_name_length": 25}
{"curie": "UMLS:C4744475", "names": ["Thyroid Gland Spindle Cell Follicular Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Spindle Cell Follicular Adenoma", "shortest_name_length": 45}
{"curie": "UMLS:C0854867", "names": ["Refractory Non-Hodgkin Lymphoma", "NonHodgkin's Lymphoma Refractory", "Refractory Non-Hodgkin's Lymphoma", "Non-Hodgkin's Lymphoma Refractory", "Non-Hodgkin's lymphoma refractory", "Non-Hodgkin's lymphoma NOS refractory"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Hodgkin's lymphoma refractory", "shortest_name_length": 31}
{"curie": "UMLS:C0740445", "names": ["EYE BURN CHEMICAL", "eye chemical burn", "burn chemical eye", "chemical burn eye", "chemical eye burn", "Burn;chemical;eye", "burn chemical eyes", "eye chemical burns", "chemical eye burns", "burns chemical eyes", "chemical burn of eye", "chemical burn to eye", "Chemical Burn of Eye", "Chemical burns of eye", "chemical burns of eye", "chemical burn of eye (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chemical burns of eye", "shortest_name_length": 17}
{"curie": "MONDO:0800152", "names": ["disorder of galactose and fructose metabolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of galactose and fructose metabolism", "shortest_name_length": 45}
{"curie": "MONDO:0010338", "names": ["SMAX3", "DSMAX", "Dsmax", "X-linked dHMN3", "X-linked dSMA3", "X-linked dHMN type 3", "X-linked dSMA type 3", "ATP7A spinal muscular atrophy", "ATP7A-related distal motor neuropathy", "X-linked distal spinal muscular atrophy 3", "SPINAL MUSCULAR ATROPHY, DISTAL, X-LINKED 3", "Spinal Muscular Atrophy, Distal, X-Linked 3", "spinal muscular atrophy, distal, X-linked 3", "X-linked distal spinal muscular atrophy type 3", "spinal muscular atrophy, distal, X-linked type 3", "X-linked recessive distal spinal muscular atrophy", "X-linked distal hereditary motor neuropathy type 3", "spinal muscular atrophy caused by mutation in ATP7A", "SPINAL MUSCULAR ATROPHY, DISTAL, X-LINKED RECESSIVE", "Spinal Muscular Atrophy, Distal, X-Linked Recessive", "spinal muscular atrophy, distal, X-linked recessive", "X-linked distal spinal muscular atrophy type 3 (disorder)", "spinal muscular atrophy, distal, X-linked 3, X-linked recessive", "ATP7A (ATPase copper transporting alpha) related distal motor neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked distal spinal muscular atrophy type 3", "shortest_name_length": 5}
{"curie": "MONDO:0004451", "names": ["sarcomatoid intrahepatic cholangiocarcinoma", "Sarcomatoid Intrahepatic Cholangiocarcinoma", "sarcomatous intrahepatic cholangiocarcinoma", "Sarcomatous Intrahepatic Cholangiocarcinoma", "intrahepatic cholangiocarcinoma with extensive sarcomatous changes", "Intrahepatic Cholangiocarcinoma with Extensive Sarcomatous Changes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sarcomatous intrahepatic cholangiocarcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0006613", "names": ["Stromal corneal pigmentation", "stromal corneal pigmentation", "corneal pigmentations stromal", "stromal corneal pigmentations", "Stromal corneal pigmentations", "Stromal corneal pigmentation (disorder)", "Stromal corneal pigmentations (diagnosis)", "stromal corneal pigmentation (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stromal corneal pigmentation", "shortest_name_length": 28}
{"curie": "UMLS:C5419092", "names": ["Refractory Primary Myelofibrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Primary Myelofibrosis", "shortest_name_length": 32}
{"curie": "MONDO:0000014", "names": ["colorblindness, partial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorblindness, partial", "shortest_name_length": 23}
{"curie": "MONDO:0002134", "names": ["sex disorder", "Sex Disorders", "sex disorders", "Sex disorders", "disorders sex", "SEX DYSFUNCTION", "sexual disorder", "Sexual disorder", "SEXUAL DISORDER", "Sexual disorders", "sexual dysfunction", "SEXUAL DYSFUNCTION", "Sexual Dysfunction", "Dysfunction;sexual", "dysfunction sexual", "Sexual dysfunction", "dysfunction, sexual", "dysfunctions sexual", "Sexual disorder NOS", "Sexual dysfunction NOS", "Sexual dysfunction, NOS", "RNDx sexual dysfunction", "Sexual function abnormal", "Impaired sexual function", "SEXUAL FUNCTION ABNORMAL", "Abnormal sexual function", "Sexual function decreased", "Decreased sexual function", "Sexual disorder (disorder)", "Impaired Sexual Functioning", "sexual disorder (diagnosis)", "Physiological Sexual Disorder", "physiological sexual disorder", "Unspecified sexual dysfunction", "sexual dysfunction (diagnosis)", "Physiological Sexual Disorders", "Sexual Disorder, Physiological", "sexual disorder, physiological", "physiological sexual disorders", "sexual disorders, physiological", "Sexual dysfunction, unspecified", "Sexual Disorders, Physiological", "Physiological Sexual Dysfunction", "physiological sexual dysfunction", "Sexual Disorders (Physiological)", "physiological sexual dysfunctions", "Physiological Sexual Dysfunctions", "Sexual Dysfunction, Physiological", "Abnormal sexual function (finding)", "sexual dysfunctions, physiological", "Sexual Dysfunctions, Physiological", "Decreased sexual function (finding)", "RNDx sexual dysfunction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "physiological sexual disorder", "shortest_name_length": 12}
{"curie": "UMLS:C3899348", "names": ["Disorder of AMH"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disorder of AMH", "shortest_name_length": 15}
{"curie": "MONDO:0019084", "names": ["Radiation proctitis", "radiation proctitis", "PROCTITIS RADIATION", "proctitis radiation", "radiation; proctitis", "proctitis; radiation", "Radiation induced proctitis", "Radiation proctitis (disorder)", "proctitis radiation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radiation proctitis", "shortest_name_length": 19}
{"curie": "MONDO:0014717", "names": ["EPM10", "early-onset Lafora body disease", "Early-onset Lafora body disease", "progressive myoclonus epilepsy 10", "EPILEPSY, PROGRESSIVE MYOCLONIC, 10", "epilepsy, progressive myoclonic, 10", "epilepsy, progressive myoclonic, type 10", "Early-onset Lafora body disease (disorder)", "Early-onset Lafora body disease (diagnosis)", "progressive familial myoclonic epilepsy early-onset Lafora body disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early-onset Lafora body disease", "shortest_name_length": 5}
{"curie": "MONDO:0020337", "names": ["CDA I", "CDA type I", "CDA type 1", "type I congenital dyserythropoietic anemia", "congenital dyserythropoietic anemia type I", "Congenital dyserythropoietic anemia type I", "Type I Congenital Dyserythropoietic Anemia", "Congenital Dyserythropoietic Anemia Type 1", "Congenital dyserythropoietic anemia type 1", "congenital dyserythropoietic anemia type 1", "Congenital dyserythropoietic anaemia type I", "Congenital Dyserythropoietic Anemia, Type I", "congenital dyserythropoietic anaemia type I", "Congenital dyserythropoietic anaemia type 1", "dyserythropoietic anemia, congenital type 1", "Dyserythropoietic Anemia, Congenital Type 1", "Congenital dyserythropoietic anemia, type I", "Anemia, Dyserythropoietic, Congenital Type 1", "Congenital dyserythropoietic anaemia, type I", "ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE I", "anemia, dyserythropoietic, congenital type 1", "Anemia, Dyserythropoietic Congenital, Type I", "Dyserythropoietic Anemia, Congenital, Type I", "Anemia, Dyserythropoietic, Congenital, Type I", "Congenital dyserythropoietic anemia, type I (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital dyserythropoietic anemia type 1", "shortest_name_length": 5}
{"curie": "MONDO:0004184", "names": ["Urethra Disease", "urethra disease", "Urethra Disorder", "Urethral Disease", "urethral disease", "urethra disorder", "urethra diseases", "disorders urethra", "Disease, Urethral", "Urethral disorder", "Urethra--Diseases", "URETHRAL DISORDER", "urethral disorder", "Urethral Diseases", "urethral diseases", "Urethral Disorder", "disorders urethral", "Urethral Disorders", "Diseases, Urethral", "disease of urethra", "Disorder of urethra", "disorder of urethra", "Urethral disorder NOS", "DISEASES OF THE URETHRA", "Disease of urethra, NOS", "Disorder of urethra, NOS", "urethra disease or disorder", "Urethral disease or syndrome", "disease or disorder of urethra", "Urethral disorder, unspecified", "disease (or disorder); urethra", "Disorder of urethra (disorder)", "disorder of urethra (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urethral disorder", "shortest_name_length": 15}
{"curie": "UMLS:C1333172", "names": ["Cutaneous Follicular Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous Follicular Lymphoma", "shortest_name_length": 29}
{"curie": "MONDO:0004689", "names": ["metal metabolism disorder", "Metal Metabolism, Inborn Error", "metal metabolism, inborn error", "Metal Metabolism, Inborn Errors", "inborn metal metabolism disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn metal metabolism disorder", "shortest_name_length": 25}
{"curie": "MONDO:0007620", "names": ["FED", "fed", "FISH-EYE DISEASE", "LCATA deficiency", "Fish-eye disease", "Fish-Eye Disease", "fish eye disease", "fish-eye disease", "disease fish-eye", "LCATA DEFICIENCY", "Fish Eye Disease", "ALPHA-LCAT DEFICIENCY", "alpha-LCAT deficiency", "FED - Fish-eye disease", "partial LCAT deficiency", "Partial LCAT deficiency", "Fish-eye disease (disorder)", "fish-eye disease (diagnosis)", "dyslipoproteinemic corneal dystrophy", "DYSLIPOPROTEINEMIC CORNEAL DYSTROPHY", "Dyslipoproteinemic Corneal Dystrophy", "Corneal Dystrophy, Dyslipoproteinemic", "alpha-lecithin:cholesterol acyltransferase deficiency", "alpha-lecithin cholesterol acyltransferase deficiency", "ALPHA-LECITHIN:CHOLESTEROL ACYLTRANSFERASE DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fish eye disease", "shortest_name_length": 3}
{"curie": "MONDO:0018626", "names": ["Paratyphoid", "paratyphoid", "PARATYPHOID", "Paratyphoid A", "paratyphoid b", "Paratyphoid C", "paratyphoid c", "Paratyphoid B", "paratyphoid a", "Paratyphoid fever", "Paratyphoid Fever", "paratyphoid fever", "Fever, Paratyphoid", "Paratyphoid Fevers", "Paratyphoid B fever", "paratyphoid A fever", "paratyphoid fever C", "Paratyphoid Fever B", "paratyphoid fever B", "paratyphoid fever A", "paratyphoid B fever", "Paratyphoid fever B", "Paratyphoid C fever", "Paratyphoid fever C", "Paratyphoid fever A", "Paratyphoid Fever C", "Fevers, Paratyphoid", "Paratyphoid A fever", "paratyphoid C fever", "Paratyphoid Fever A", "C; paratyphoid fever", "paratyphoid fever; A", "B; paratyphoid fever", "A; paratyphoid fever", "paratyphoid fever; C", "paratyphoid fever; B", "Paratyphoid fever, NOS", "type A paratyphoid fever", "paratyphoid fever type A", "paratyphoid fever type C", "type C paratyphoid fever", "paratyphoid fever type B", "type B paratyphoid fever", "Paratyphoid fever (disorder)", "paratyphoid fever (diagnosis)", "Salmonella; paratyphoid fever", "Paratyphoid fever, unspecified", "Salmonella paratyphi infection", "Paratyphoid B fever (disorder)", "Paratyphoid C fever (disorder)", "Paratyphoid A fever (disorder)", "Salmonella; paratyphoid fever A", "Salmonella; paratyphoid fever C", "Salmonella; paratyphoid fever B", "infection; Salmonella, paratyphi", "Salmonella; infection, paratyphi", "paratyphoid fever type C (diagnosis)", "paratyphoid fever type A (diagnosis)", "paratyphoid fever type B (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paratyphoid fever", "shortest_name_length": 11}
{"curie": "UMLS:C4553241", "names": ["Stage II Renal Pelvis and Ureter Cancer", "stage II renal pelvis and ureter cancer AJCC v8", "Stage II Renal Pelvis and Ureter Cancer AJCC v8", "Stage II Renal Pelvis and Ureter Urothelial Carcinoma AJCC v8", "stage II renal pelvis and ureter urothelial carcinoma AJCC v8", "stage II transitional cell cancer of the renal pelvis and ureter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Renal Pelvis and Ureter Cancer AJCC v8", "shortest_name_length": 39}
{"curie": "MONDO:0004888", "names": ["Partial circumpapillary choroid dystrophy", "partial circumpapillary choroid dystrophy", "Partial circumpapillary dystrophy of choroid", "Circumpapillary dystrophy of choroid, partial", "Partial circumpapillary choroid dystrophy (disorder)", "partial circumpapillary hereditary choroidal dystrophy", "partial circumpapillary hereditary choroidal dystrophy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial circumpapillary choroid dystrophy", "shortest_name_length": 41}
{"curie": "MONDO:0008049", "names": ["infantile-onset distal myopathy", "myopathy, distal, infantile-onset", "MYOPATHY, DISTAL, INFANTILE-ONSET", "Myopathy, Distal, with Onset in Infancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy, distal, infantile-onset", "shortest_name_length": 31}
{"curie": "MONDO:0018531", "names": ["liver cancer", "Liver Cancer", "hepatic cancer", "cancer of liver", "Cancer of Liver", "liver carcinoma", "Liver Carcinoma", "carcinoma of liver", "Cancer of the Liver", "cancer of the liver", "Biliary Tract Cancer", "Primary Liver Carcinoma", "primary liver carcinoma", "liver/hepatobiliary cancer", "carcinoma of liver and IBT", "Liver/hepatobiliary cancer", "Liver and hepatobiliary cancer, NOS", "liver and intrahepatic bile duct cancer", "Liver and Intrahepatic Bile Duct Cancer", "Liver and Intrahepatic Bile Duct Carcinoma", "liver and intrahepatic bile duct carcinoma", "Liver and Intrahepatic Biliary Tract Cancer", "liver and intrahepatic biliary tract cancer", "Cancer of Liver and Intrahepatic Biliary Tract", "cancer of liver and intrahepatic biliary tract", "Liver and Intrahepatic Biliary Tract Carcinoma", "liver and intrahepatic biliary tract carcinoma", "carcinoma of liver and intrahepatic biliary tract", "cancer of the liver and intrahepatic biliary tract", "Cancer of the Liver and Intrahepatic Biliary Tract", "hepatocellular carcinoma plus intrahepatic cholangiocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma of liver and intrahepatic biliary tract", "shortest_name_length": 12}
{"curie": "MONDO:0014289", "names": ["MRT41", "macrocephaly-developmental delay syndrome", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 41", "mental retardation, autosomal recessive 41", "intellectual disability, autosomal recessive 41", "mental retardation, autosomal recessive type 41", "intellectual disability, autosomal recessive type 41", "autosomal recessive intellectual developmental disorder 41", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 41"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macrocephaly-developmental delay syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0100008", "names": ["FPIES", "delayed food allergy", "food protein-induced enterocolitis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "food protein-induced enterocolitis syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0376384", "names": ["Nicotine Use Disorder", "Nicotine Use Disorders", "Disorder, Nicotine Use", "Nicotine-related disorder", "nicotine-related disorders", "Nicotine-related disorder, NOS", "Nicotine induced mental disorder", "nicotine-related disorders (diagnosis)", "Nicotine-induced organic mental disorder", "Nicotine-induced organic mental disorder, NOS", "Nicotine-induced organic mental disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nicotine Use Disorder", "shortest_name_length": 21}
{"curie": "UMLS:C0877855", "names": ["Cerebral embolism and thrombosis", "Cerebral Embolism and Thrombosis", "Cerebrovascular embolism and thrombosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebral Embolism and Thrombosis", "shortest_name_length": 32}
{"curie": "UMLS:C4288545", "names": ["Ovarian Adenomatoid Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Adenomatoid Tumor", "shortest_name_length": 25}
{"curie": "MONDO:0020417", "names": ["PRAA", "right aortic arch", "Right aortic arch", "Right Aortic Arch", "right-sided aortic arch", "Right-sided aortic arch", "Aberrant right aortic arch", "right aortic arch (disease)", "Persistent right aortic arch", "Right aortic arch (disorder)", "right aortic arch; persistent", "persistent; right aortic arch", "Structure of right aortic arch", "right-sided aortic arch (diagnosis)", "Structure of right aortic arch (body structure)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "right aortic arch", "shortest_name_length": 4}
{"curie": "UMLS:C5419537", "names": ["Unresectable Pancreatic Ductal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Pancreatic Ductal Adenocarcinoma", "shortest_name_length": 45}
{"curie": "UMLS:C5421292", "names": ["Sinonasal Schwannoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Schwannoma", "shortest_name_length": 20}
{"curie": "MONDO:0020569", "names": ["intermediate DEND syndrome", "developmental delay-epilepsy-neonatal diabetes syndrome, intermediate form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intermediate DEND syndrome", "shortest_name_length": 26}
{"curie": "UMLS:C2986673", "names": ["Stage IV Liver Cancer", "Stage IV Adult Liver Cancer AJCC v7", "stage IV adult primary liver cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Adult Liver Cancer AJCC v7", "shortest_name_length": 21}
{"curie": "MONDO:0000863", "names": ["MSA", "MLASA", "mitochondrial myopathy and sideroblastic anemia", "sideroblastic anemia and mitochondrial myopathy", "myopathy, lactic acidosis and sideroblastic anemia", "myopathy, lactic acidosis, and siderblastic anemia", "myopathy, lactic acidosis, and sideroblastic anemia", "Myopathy with lactic acidosis and sideroblastic anemia", "myopathy with lactic acidosis and sideroblastic anemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy, lactic acidosis, and sideroblastic anemia", "shortest_name_length": 3}
{"curie": "MONDO:0030883", "names": ["CTS2", "carpal tunnel syndrome 2", "CARPAL TUNNEL SYNDROME 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carpal tunnel syndrome 2", "shortest_name_length": 4}
{"curie": "UMLS:C4287827", "names": ["Ovarian Cancer by FIGO Stage", "Ovarian Carcinoma by FIGO Stage 2014"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Cancer by FIGO Stage", "shortest_name_length": 28}
{"curie": "UMLS:C1334050", "names": ["HPV-Related Carcinoma", "HPV-related carcinoma", "Human Papillomavirus-Related Carcinoma", "Human Papilloma Virus Related Carcinoma", "Human Papilloma Virus-Related Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HPV-related carcinoma", "shortest_name_length": 21}
{"curie": "MONDO:0006165", "names": ["colorectal squamous cell cancer", "Colorectal Squamous Cell Carcinoma", "colorectal squamous cell carcinoma", "colorectum squamous cell carcinoma", "colorectal (colon or rectal) squamous cell cancer", "Colorectal (Colon or Rectal) Squamous Cell Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorectal squamous cell carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0000340", "names": ["bulbospinal polio"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bulbospinal polio", "shortest_name_length": 17}
{"curie": "MONDO:0012815", "names": ["CRMCC", "COATS PLUS SYNDROME", "Coats plus syndrome", "Coats Plus Syndrome", "cerebroretinal microangiopathy with calcfications and cysts", "Cerebroretinal microangiopathy with calcifications and cysts", "Cerebroretinal Microangiopathy with Calcifications and Cysts", "cerebroretinal microangiopathy with calcifications and cysts", "Cerebroretinal microangiopathy with calcifications and cysts (disorder)", "CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Coats plus syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0010938", "names": ["JAK3 Deficiency", "JAK3 deficiency", "T-B+ SCID due to JAK3 deficiency", "SCID, autosomal recessive, T-negative/B-positive type", "SCID, T cell-negative, B cell-positive, NK cell-negative", "SCID, T Cell-Negative, B Cell-Positive, NK Cell-Negative", "SCID, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-NEGATIVE", "T-B+ severe combined immunodeficiency due to JAK3 deficiency", "T-cell negative B-cell positive severe combined immunodeficiency due to JAK3 deficiency", "severe combined immunodeficiency T-cell negative B-cell positive due to janus kinase-3 deficiency", "Severe combined immunodeficiency T-cell negative B-cell positive due to janus kinase-3 deficiency", "T-cell negative B-cell positive severe combined immunodeficiency due to Janus kinase-3 deficiency", "Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, NK Cell-Negative", "SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-NEGATIVE", "Severe Combined Immunodeficiency, Autosomal Recessive, T-Cell Negative, B-Cell Positive, NK-Cell Negative", "severe combined immunodeficiency, autosomal recessive, T cell-NEGATIVE, B cell-POSITIVE, NK cell-NEGATIVE", "Severe combined immunodeficiency T-cell negative B-cell positive due to janus kinase-3 deficiency (disorder)", "T-cell negative B-cell positive severe combined immunodeficiency due to Janus kinase-3 deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-B+ severe combined immunodeficiency due to JAK3 deficiency", "shortest_name_length": 15}
{"curie": "UMLS:C0588014", "names": ["Malignant neoplasm of unknown primary site", "Primary malignant neoplasm of unknown site", "malignant neoplasm primary of unknown site", "Primary malignant neoplasm of unknown site (disorder)", "Primary malignant neoplasm of unknown site (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary malignant neoplasm of unknown site", "shortest_name_length": 42}
{"curie": "MONDO:0009344", "names": ["Al Gazali Hirschsprung syndrome", "Al Gazali Donnai Muller syndrome", "Al Gazali-Donnai-Muller syndrome", "Al-Gazali-Donnai-Mueller syndrome", "Al Gazali Donnai Mueller syndrome", "Hirschsprung disease with nail hypoplasia and dysmorphism", "Hirschsprung disease-nail hypoplasia-dysmorphism syndrome", "Hirschsprung disease with nail hypoplasia and dysmorphism (disorder)", "Hirschsprung's disease, hypoplastic nails, and minor dysmorphic features", "Hirschsprung's disease, hypoplastic nails, and dysmorphic facial features", "Hirschsprung disease with hypoplastic nails and dysmorphic facial features", "Hirschsprung Disease with Hypoplastic Nails and Dysmorphic Facial Features", "HIRSCHSPRUNG DISEASE WITH HYPOPLASTIC NAILS AND DYSMORPHIC FACIAL FEATURES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hirschsprung disease-nail hypoplasia-dysmorphism syndrome", "shortest_name_length": 31}
{"curie": "MONDO:0019529", "names": ["radiation myelitis", "Myelopathy radiation", "radiation myelopathy", "RADIATION MYELOPATHY", "Radiation myelopathy", "radiation; myelopathy", "delayed radiation myelopathy", "Radiation-Induced Myelopathy", "Radiation-induced myelopathy", "Myelopathy, radiation-induced", "myelopathy; radiation-induced", "radiation myelopathy (diagnosis)", "Radiation-induced myelopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radiation myelitis", "shortest_name_length": 18}
{"curie": "MONDO:0009429", "names": ["hypophosphatemia, renal, with intracerebral calcifications", "HYPOPHOSPHATEMIA, RENAL, WITH INTRACEREBRAL CALCIFICATIONS", "Hypophosphatemia, Renal, with Intracerebral Calcifications"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypophosphatemia, renal, with intracerebral calcifications", "shortest_name_length": 58}
{"curie": "MONDO:0033816", "names": ["thygeson superficial punctate keratopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thygeson superficial punctate keratopathy", "shortest_name_length": 41}
{"curie": "UMLS:C4055243", "names": ["Childhood Periosteal Osteosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Periosteal Osteosarcoma", "shortest_name_length": 33}
{"curie": "UMLS:C0015951", "names": ["Fetal Resorption", "Fetal resorption", "Foetal resorption", "Fetal Resorptions", "Resorption, Fetal", "Resorptions, Fetal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fetal Resorption", "shortest_name_length": 16}
{"curie": "UMLS:C1336406", "names": ["Stage IVC Oropharynx Carcinoma", "Stage IVC Oropharyngeal Carcinoma", "Stage IVC Carcinoma of Oropharynx", "Stage IVC Carcinoma of the Oropharynx", "Stage IVC Oropharyngeal Throat Cancer", "Stage IVC Oropharyngeal Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Oropharyngeal Carcinoma AJCC v7", "shortest_name_length": 30}
{"curie": "UMLS:C2983716", "names": ["Lung Cancer by AJCC v6 Stage", "Lung Carcinoma by AJCC v6 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Cancer by AJCC v6 Stage", "shortest_name_length": 28}
{"curie": "MONDO:0032681", "names": ["PEERB", "ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH EPISODIC RHABDOMYOLYSIS", "encephalopathy, progressive, early-onset, with episodic rhabdomyolysis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephalopathy, progressive, early-onset, with episodic rhabdomyolysis", "shortest_name_length": 5}
{"curie": "UMLS:C0280163", "names": ["high-grade, stage III adult NHL", "adult NHL, stage III, high grade", "NHL, high grade, stage III adult", "Stage III High Grade Adult Non-Hodgkin's Lymphoma", "non-Hodgkin's lymphoma, high grade, stage III adult", "adult non-Hodgkin's lymphoma, high grade, stage III", "lymphoma, high grade, stage III adult non-Hodgkin's"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III High Grade Adult Non-Hodgkin's Lymphoma", "shortest_name_length": 31}
{"curie": "OMIM:616604", "names": ["Dup(14)q(32)", "Trisomy 14q32", "14q32 duplication syndrome", "14q32 duplication syndrome (disorder)", "CHROMOSOME 14q32 DUPLICATION SYNDROME, 700-KB", "MYELOPROLIFERATIVE NEOPLASMS, FAMILIAL, SUSCEPTIBILITY TO", "Predisposition to adult-onset myeloproliferative neoplasm due to 14q32 duplication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 12}
{"curie": "UMLS:C0347222", "names": ["Benign Nasal Sinus Tumor", "Benign Tumor of Nasal Sinus", "Benign Nasal Sinus Neoplasm", "Benign Accessory Sinus Tumor", "Benign Paranasal Sinus Tumor", "Benign tumor of nasal sinuses", "Benign Neoplasm of Nasal Sinus", "Benign tumour of nasal sinuses", "Benign neoplasm of nasal sinus", "Benign Paranasal Sinus Neoplasm", "Paranasal sinus benign neoplasm", "benign accessory sinus neoplasm", "benign tumor of accessory sinus", "Benign Tumor of Paranasal Sinus", "Benign Accessory Sinus Neoplasm", "Benign Tumor of Accessory Sinus", "Benign Tumor of the Nasal Sinus", "Benign Neoplasm of Accessory Sinus", "Benign neoplasm of accessory sinus", "Benign Neoplasm of the Nasal Sinus", "Benign Neoplasm of Paranasal Sinus", "benign neoplasm of accessory sinus", "Benign Tumor of the Paranasal Sinus", "Benign Tumor of the Accessory Sinus", "Benign Neoplasm of the Paranasal Sinus", "Benign Neoplasm of the Accessory Sinus", "Benign neoplasm of accessory sinus, NOS", "Benign neoplasm of accessory sinus (disorder)", "benign neoplasm of accessory sinus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign neoplasm of accessory sinus", "shortest_name_length": 24}
{"curie": "MONDO:0015278", "names": ["Familial Pancreatic Cancer", "familial pancreatic cancer", "pancreatic cancer, somatic", "Familial pancreatic cancer", "pancreatic acinar carcinoma", "pancreatic cancer, familial", "hereditary pancreatic cancer", "Hereditary Pancreatic Cancer", "pancreatic cancer, hereditary", "pancreatic carcinoma, somatic", "Familial Pancreatic carcinoma", "Familial Pancreatic Carcinoma", "Familial pancreatic carcinoma", "familial pancreatic carcinoma", "Pancreatic carcinoma, familial", "Hereditary Pancreatic Carcinoma", "hereditary pancreatic carcinoma", "Familial pancreatic cancer syndrome", "pancreatic malignant neoplasm familial", "Familial malignant neoplasm of pancreas", "hereditary exocrine pancreatic carcinoma", "Familial malignant neoplasm of pancreas (disorder)", "Familial malignant neoplasm of pancreas (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial pancreatic carcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0020554", "names": ["Heiner syndrome", "Cow's milk hypersensitivity", "cow's milk hypersensitivity", "Milk-induced pulmonary disease in infant", "Milk-induced pulmonary disease in infant (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Heiner syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0011651", "names": ["IDDSFAS", "Mental Retardation, Short Stature, Facial Anomalies, and Joint Dislocations", "MENTAL RETARDATION, SHORT STATURE, FACIAL ANOMALIES, AND JOINT DISLOCATIONS", "mental retardation, short stature, facial anomalies, and JOINT dislocations", "intellectual disability, short stature, facial anomalies, and JOINT dislocations", "intellectual disability, short stature, facial anomalies, and joint dislocations", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH SHORT STATURE, FACIAL ANOMALIES, AND SPEECH DEFECTS", "intellectual developmental disorder with short stature, facial anomalies, and speech defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, short stature, facial anomalies, and joint dislocations", "shortest_name_length": 7}
{"curie": "MONDO:0005901", "names": ["pasteurellosis", "Pasteurellosis", "Pasteurelloses", "PASTEURELLOSES", "shipping fever", "Transport fever", "Pasteurellosis, NOS", "Pasteurella Infection", "Pasteurella infection", "pasteurella infection", "Pasteurella; infection", "infection; Pasteurella", "Pasteurella Infections", "Infection, Pasteurella", "Pasteurella infections", "Infections, Pasteurella", "Pasteurella infection, NOS", "Pasteurella infectious disease", "infectious disease pasteurella", "Pasteurella disease or disorder", "Pasteurella infection (disorder)", "Pasteurella infection (diagnosis)", "Pasteurella caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pasteurellosis", "shortest_name_length": 14}
{"curie": "MONDO:0043735", "names": ["osteoradionecrosis", "Osteoradionecrosis", "Osteoradionecroses", "Radiation necrosis of bone", "radiation necrosis of bone", "Osteoradionecrosis (disorder)", "osteoradionecrosis (diagnosis)", "injury radiation osteoradionecrosis", "Osteonecrosis caused by ionising radiation", "Osteonecrosis caused by ionizing radiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteoradionecrosis", "shortest_name_length": 18}
{"curie": "MONDO:0014551", "names": ["SNSK", "short stature with nonspecific skeletal abnormalities", "SHORT STATURE WITH NONSPECIFIC SKELETAL ABNORMALITIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short stature with nonspecific skeletal abnormalities", "shortest_name_length": 4}
{"curie": "MONDO:0024336", "names": ["vulva adenocarcinoma", "Vulvar Adenocarcinoma", "Vulvar adenocarcinoma", "vulvar adenocarcinoma", "Adenocarcinoma of Vulva", "adenocarcinoma of vulva", "adenocarcinoma of Vulva", "Adenocarcinoma of the vulva", "adenocarcinoma of the vulva", "Adenocarcinoma of the Vulva", "mammalian vulva adenocarcinoma", "adenocarcinoma of vulva (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar adenocarcinoma", "shortest_name_length": 20}
{"curie": "MONDO:0027451", "names": ["ARCL2D", "autosomal recessive cutis laxa type 2D", "autosomal recessive cutis laxa type IID", "cutis laxa, autosomal recessive, type 2D", "cutis laxa, autosomal recessive, type IID", "CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive cutis laxa type 2D", "shortest_name_length": 6}
{"curie": "UMLS:C4526727", "names": ["Stage IVB Lung Cancer", "Stage IVB Lung Cancer AJCC v8", "stage IVB lung cancer AJCC v8", "stage IVB non-small cell lung cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Lung Cancer AJCC v8", "shortest_name_length": 21}
{"curie": "MONDO:0007537", "names": ["Lms", "LMS", "LMNS", "Lehman syndrome", "LEHMAN SYNDROME", "Lehman Syndrome", "LATERAL MENINGOCELE SYNDROME", "lateral meningocele syndrome", "Lateral meningocele syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lateral meningocele syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C2981236", "names": ["Stage III Rectosigmoid Cancer", "Stage III Rectosigmoid Cancer AJCC v6", "Stage III Rectosigmoid Carcinoma AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Rectosigmoid Cancer AJCC v6", "shortest_name_length": 29}
{"curie": "UMLS:C1336116", "names": ["Stage IA Large Cell Lung Cancer", "Stage IA Large Cell Lung Carcinoma", "Stage IA Large Cell Carcinoma of Lung", "Stage IA Large Cell Carcinoma of the Lung", "Stage IA Lung Large Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Lung Large Cell Carcinoma AJCC v7", "shortest_name_length": 31}
{"curie": "UMLS:C5204786", "names": ["Advanced Malignant Thymoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Malignant Thymoma", "shortest_name_length": 26}
{"curie": "MONDO:0005289", "names": ["Tumor of nasal sinus", "Tumour of nasal sinus", "accessory sinus tumor", "Accessory Sinus Tumor", "Paranasal Sinus Tumor", "paranasal sinus tumor", "neoplasm of nasal sinus", "tumor of paranasal sinus", "Paranasal Sinus Neoplasm", "tumor of Accessory sinus", "Accessory Sinus Neoplasm", "Tumor of paranasal sinus", "paranasal sinus neoplasm", "tumor of accessory sinus", "Tumor of Paranasal Sinus", "accessory sinus neoplasm", "Tumor of Accessory Sinus", "Paranasal sinus neoplasm", "Paranasal Sinus Neoplasms", "Tumour of paranasal sinus", "paranasal sinus neoplasms", "Neoplasm, Paranasal Sinus", "Neoplasms, Paranasal Sinus", "neoplasm of accessory sinus", "Neoplasm of Paranasal Sinus", "neoplasm of paranasal sinus", "Neoplasm of accessory sinus", "Neoplasm of Accessory Sinus", "Tumor of the Paranasal Sinus", "tumor of the accessory sinus", "tumor of the paranasal sinus", "Tumor of the Accessory Sinus", "Tumor of the paranasal sinuses", "paranasal sinus benign neoplasm", "Tumour of the paranasal sinuses", "neoplasm of the accessory sinus", "Neoplasm of the Accessory Sinus", "Neoplasm of the Paranasal Sinus", "neoplasm of the paranasal sinus", "Neoplasm of the paranasal sinuses", "paranasal sinus neoplasm (disease)", "neoplasm of nasal sinus (diagnosis)", "Neoplasm of accessory sinus (disorder)", "neoplasm of accessory sinus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paranasal sinus neoplasm", "shortest_name_length": 20}
{"curie": "MONDO:0022399", "names": ["retinal ciliopathy due to mutation in the RPGR gene"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal ciliopathy due to mutation in the RPGR gene", "shortest_name_length": 51}
{"curie": "MONDO:0020664", "names": ["spindle cell tumor", "Spindle Cell Tumor", "spindle cell neoplasm", "Spindle Cell Neoplasm", "spindle cell neoplasm of penis", "spindle cell neoplasm of penis (diagnosis)", "penile neoplasm malignant spindle cell type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spindle cell neoplasm", "shortest_name_length": 18}
{"curie": "UMLS:C1274228", "names": ["Chylomicronemia syndrome", "Chylomicronemia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chylomicronemia syndrome", "shortest_name_length": 24}
{"curie": "EFO:0009093", "names": ["choroidal melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choroidal melanoma", "shortest_name_length": 18}
{"curie": "UMLS:C4520989", "names": ["Stage 0 Laryngeal Cancer AJCC v8", "Larynx Epidermoid Carcinoma in situ", "Stage 0 Laryngeal Carcinoma AJCC v8", "Stage 0 Larynx Epidermoid Carcinoma", "Stage 0 Laryngeal Epidermoid Carcinoma", "Epidermoid Carcinoma in situ of Larynx", "Stage 0 Larynx Squamous Cell Carcinoma", "Larynx Squamous Cell Carcinoma in situ", "Laryngeal Epidermoid Carcinoma in situ", "Stage 0 Epidermoid Carcinoma of Larynx", "Stage 0 Laryngeal Squamous Cell Carcinoma", "Laryngeal Squamous Cell Carcinoma in situ", "Squamous Cell Carcinoma in situ of Larynx", "Stage 0 Squamous Cell Carcinoma of Larynx", "Stage 0 Epidermoid Carcinoma of the Larynx", "Epidermoid Carcinoma in situ of the Larynx", "Stage 0 Laryngeal Throat Squamous Cell Cancer", "Squamous Cell Carcinoma in situ of the Larynx", "Stage 0 Squamous Cell Carcinoma of the Larynx", "Stage 0 Laryngeal Squamous Cell Carcinoma AJCC v7", "Stage 0 Laryngeal Squamous Cell Carcinoma AJCC v8", "Stage 0 Laryngeal Squamous Cell Carcinoma AJCC v6", "Stage 0 Laryngeal Squamous Cell Carcinoma AJCC v6, v7, and v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Laryngeal Squamous Cell Carcinoma AJCC v6, v7, and v8", "shortest_name_length": 32}
{"curie": "MONDO:0700176", "names": ["feline lymphoma", "Feline Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "feline lymphoma", "shortest_name_length": 15}
{"curie": "UMLS:C5555332", "names": ["Immunosuppressive Disorder", "Immunosuppressive_conditions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immunosuppressive Disorder", "shortest_name_length": 26}
{"curie": "MONDO:0010833", "names": ["HSCR2", "EDNRB Hirschsprung disease", "Hirschsprung disease type 2", "susceptibility to Hirschsprung disease 2", "Hirschsprung disease, susceptibility to, 2", "HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 2", "Hirschsprung disease, susceptibility to, type 2", "Hirschsprung disease caused by mutation in EDNRB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hirschsprung disease, susceptibility to, 2", "shortest_name_length": 5}
{"curie": "MONDO:0021522", "names": ["benign tumor of mandible", "benign neoplasm of mandible", "Benign neoplasm of mandible", "benign tumor of lower jaw bone", "benign neoplasm of lower jaw bone", "bone of lower jaw benign neoplasm", "Benign Neoplasm of Lower Jaw Bone", "Benign neoplasm of lower jaw bone", "Benign neoplasm of mandible (disorder)", "benign neoplasm of mandible (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of lower jaw bone", "shortest_name_length": 24}
{"curie": "MONDO:0012080", "names": ["HMN2B", "DHMN2B", "HMN 2B", "HMN IIB", "distal hereditary motor neuropathy type 2B", "HSPB1 neuronopathy, distal hereditary motor", "distal hereditary motor neuropathy type IIB", "neuropathy, distal hereditary motor, type 2B", "Neuropathy, Distal Hereditary Motor, Type IIB", "NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IIB", "neuronopathy, distal hereditary motor, type 2B", "NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIB", "Neuronopathy, Distal Hereditary Motor, Type IIB", "neuronopathy, distal hereditary motor, type IIB", "neuronopathy, distal hereditary motor caused by mutation in HSPB1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuronopathy, distal hereditary motor, type 2B", "shortest_name_length": 5}
{"curie": "UMLS:C4553672", "names": ["Stage IIIA Ovarian Cancer", "Stage IIIA Ovarian Cancer AJCC v8", "Stage IIIA Ovarian Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Ovarian Cancer AJCC v8", "shortest_name_length": 25}
{"curie": "UMLS:C0280353", "names": ["Stage III Lip and Oral Cavity Squamous Cell Cancer", "Stage III Lip and Oral Cavity Squamous Cell Carcinoma", "lip and oral cavity squamous cell carcinoma, stage III", "oral cavity and lip squamous cell carcinoma, stage III", "epidermoid carcinoma of the lip and oral cavity, stage III", "stage III squamous cell carcinoma of the lip and oral cavity", "Stage III Lip and Oral Cavity Squamous Cell Carcinoma AJCC v7", "Stage III Lip and Oral Cavity Squamous Cell Carcinoma AJCC v6", "squamous cell carcinoma of the lip and oral cavity, stage III", "Stage III Lip and Oral Cavity Squamous Cell Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Lip and Oral Cavity Squamous Cell Carcinoma AJCC v6 and v7", "shortest_name_length": 50}
{"curie": "MONDO:0011457", "names": ["ATLD", "ATLD1", "Ataxia Telangiectasia Like Disorder", "ataxia-telangiectasia-like disorder", "ataxia-telangiectasia-like disorder 1", "ataxia - telangiectasia-like disorder", "ataxia-telangiectasia-like disorder type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ataxia-telangiectasia-like disorder", "shortest_name_length": 4}
{"curie": "UMLS:C0275686", "names": ["Neonatal listeriosis", "congenital listeriosis", "Congenital listeriosis", "Congenital Listeriosis", "congenital; listeriosis", "listeriosis; congenital", "Congenital listeriosis (disorder)", "congenital listeriosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital listeriosis", "shortest_name_length": 20}
{"curie": "MONDO:0016736", "names": ["RGNT", "DNT of the cerebellum", "Rosette-Forming Glioneuronal Tumor", "rosette-forming glioneuronal tumor", "Rosette-forming glioneuronal tumor", "Rosette-forming glioneuronal tumour", "Rosette-forming glioneuronal neoplasm", "Rosette-forming glioneuronal neoplasm (disorder)", "dysembryoplastic neuroepithelial tumor of cerebellum", "rosette-forming glioneuronal tumor of fourth ventricule", "Rosette-forming glioneuronal tumor of the fourth ventricle", "Rosette-Forming Glioneuronal Tumor of the Fourth Ventricle", "Rosette-forming glioneuronal tumour of the fourth ventricle", "Rosette-forming glioneuronal neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rosette-forming glioneuronal tumor of fourth ventricule", "shortest_name_length": 4}
{"curie": "UMLS:C0178324", "names": ["vascular injury", "Vascular injury", "Vascular Injury", "Injury, Vascular", "Vascular injuries", "vascular injuries", "Vascular Injuries", "Injuries, Vascular", "injury blood vessel", "BLOOD VESSEL INJURY", "Vascular injury NOS", "blood vessel injury", "blood vessel; injury", "injury; blood vessel", "blood injuries vessel", "injury of blood vessel", "Vascular System Injury", "Injury of blood vessel", "Injury, Vascular System", "System Injury, Vascular", "INJURY TO BLOOD VESSELS", "Vascular System Injuries", "Injuries, Vascular System", "System Injuries, Vascular", "Injury to blood vessel NOS", "Injury of blood vessel, NOS", "INJURIES OF THE BLOOD VESSELS", "Injury of blood vessel (disorder)", "injury of blood vessel (diagnosis)", "Injury to blood vessels of unspecified site", "Injury of blood vessel(s) of unspecified body region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vascular System Injuries", "shortest_name_length": 15}
{"curie": "UMLS:C1142174", "names": ["stenosis shunt", "Shunt stenosis", "shunt stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Shunt stenosis", "shortest_name_length": 14}
{"curie": "UMLS:C0866110", "names": ["Nephrotic Syndrome with Lesion of Segmental Hyalinosis", "Nephrotic syndrome with lesion of segmental hyalinosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome with Lesion of Segmental Hyalinosis", "shortest_name_length": 54}
{"curie": "UMLS:C0347015", "names": ["Metastasis to pituitary", "Metastases to pituitary gland", "Metastasis to Pituitary Gland", "Cancer metastatic to pituitary gland", "Metastatic Neoplasm to the Pituitary Gland", "Secondary malignant neoplasm of pituitary gland", "Metastatic malignant neoplasm to pituitary gland", "Metastatic malignant neoplasm of pituitary gland", "Metastatic Malignant Neoplasm to the Pituitary Gland", "Metastatic Malignant Neoplasm in the Pituitary Gland", "pituitary neoplasm malignant of pituitary gland secondary", "Secondary malignant neoplasm of pituitary gland (diagnosis)", "Metastatic malignant neoplasm to pituitary gland (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to pituitary gland", "shortest_name_length": 23}
{"curie": "MONDO:0010506", "names": ["TOKAS", "MRX61", "TONNE-KALSCHEUER SYNDROME", "Tonne-Kalscheuer syndrome", "X-linked mental retardation 61", "MENTAL RETARDATION, X-LINKED 61", "mental retardation, X-linked 61", "intellectual disability, X-linked 61", "mental retardation, X-linked type 61", "intellectual disability, X-linked type 61", "RLIM non-syndromic X-linked intellectual disability", "non-syndromic X-linked intellectual disability caused by mutation in RLIM", "intellectual developmental disorder with or without hand and foot anomalies, genital anomalies, or congenital diaphragmatic hernia", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT HAND AND FOOT ANOMALIES, GENITAL ANOMALIES, OR CONGENITAL DIAPHRAGMATIC HERNIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 61", "shortest_name_length": 5}
{"curie": "UMLS:C4526630", "names": ["Pleural Malignant Mesothelioma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pleural Malignant Mesothelioma by AJCC v7 Stage", "shortest_name_length": 47}
{"curie": "UMLS:C3275121", "names": ["ONE VESSEL DISEASE", "One Vessel Coronary Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "One Vessel Coronary Disease", "shortest_name_length": 18}
{"curie": "UMLS:C0346998", "names": ["Vulvar Metastasis", "Metastasis to the Vulva", "Cancer metastatic to vulva", "Secondary cancer of the vulva", "Metastatic Neoplasm to the Vulva", "vulvar neoplasm malignant secondary", "Secondary malignant neoplasm of vulva", "Malignant neoplasm of vulva metastatic", "Metastatic malignant neoplasm to vulva", "Metastatic malignant neoplasm of vulva", "Metastatic Malignant Neoplasm to the Vulva", "Metastatic Malignant Neoplasm in the Vulva", "Secondary malignant neoplasm of vulva, NOS", "Metastatic malignant neoplasm to vulva, NOS", "Secondary malignant neoplasm of vulva (diagnosis)", "Metastatic malignant neoplasm to vulva (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary malignant neoplasm of vulva", "shortest_name_length": 17}
{"curie": "MONDO:0007463", "names": ["DISTAL OSTEOSCLEROSIS", "Distal Osteosclerosis", "distal osteosclerosis", "Osteosclerosis, Distal", "osteosclerosis, distal", "OSTEOSCLEROSIS, DISTAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal osteosclerosis", "shortest_name_length": 21}
{"curie": "UMLS:C0855107", "names": ["Burkitt's tumor stage II", "Burkitt's tumour stage II", "Stage II Burkitt Lymphoma", "Burkitt's lymphoma stage II", "Burkitt's Lymphoma Stage II", "Stage II Burkitt's Lymphoma", "Ann Arbor Stage II Burkitt Lymphoma", "Burkitt's tumor or lymphoma stage II", "Burkitt's tumour or lymphoma stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Burkitt Lymphoma", "shortest_name_length": 24}
{"curie": "UMLS:C3897021", "names": ["Untreated Oligoastrocytoma", "untreated childhood oligoastrocytoma", "Untreated Childhood Oligoastrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Untreated Childhood Oligoastrocytoma", "shortest_name_length": 26}
{"curie": "UMLS:C1832567", "names": ["LGMD1C", "Limb-Girdle Muscular Dystrophy Type 1C", "Muscular Dystrophy, Limb-Girdle, Type 1C", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1C"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1C", "shortest_name_length": 6}
{"curie": "MONDO:0012446", "names": ["SEBORRHEA-LIKE DERMATITIS WITH PSORIASIFORM ELEMENTS", "seborrhea-like dermatitis with psoriasiform elements", "Seborrhea-like dermatitis with psoriasiform elements", "Seborrhea-Like Dermatitis with Psoriasiform Elements", "Seborrhoea-like dermatitis with psoriasiform elements", "Seborrhea-like dermatitis with psoriasiform elements (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "seborrhea-like dermatitis with psoriasiform elements", "shortest_name_length": 52}
{"curie": "UMLS:C0877013", "names": ["Restrictive pulmonary disease", "restrictive pulmonary disease", "pulmonary restrictive disease", "diseases pulmonary restrictive", "Restrictive pulmonary ventilation dysfunction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Restrictive pulmonary disease", "shortest_name_length": 29}
{"curie": "UMLS:C1541566", "names": ["Ependymal Tumor", "Adult Ependymal Tumor", "adult ependymal tumors", "Brain tumor, adult: Ependymoma/Ependymal tumors"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Ependymal Tumor", "shortest_name_length": 15}
{"curie": "UMLS:C0349650", "names": ["Non-tuberculous mycobacterial pneumonia", "Non-tuberculous mycobacterial pneumonia (disorder)", "Non-tuberculous mycobacterial pneumonia (diagnosis)", "atypical mycobacterial infection non-tuberculous pneumonia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-tuberculous mycobacterial pneumonia", "shortest_name_length": 39}
{"curie": "UMLS:C4525258", "names": ["Stage 0 Intrahepatic Bile Duct Cancer", "Stage 0 Intrahepatic Bile Duct Cancer AJCC v8", "Stage 0 Intrahepatic Bile Duct Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Intrahepatic Bile Duct Cancer AJCC v8", "shortest_name_length": 37}
{"curie": "UMLS:C0161801", "names": ["Lung transplant disorder", "lung transplant; complications", "complications; lung transplant", "Transplanted Lung Complication", "Complications of lung transplant", "complications of lung transplant", "Complication of Transplanted Lung", "Complication of transplanted lung", "Complications of transplanted lung", "complications of lung transplant (diagnosis)", "Complication of transplanted lung (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Complication of transplanted lung", "shortest_name_length": 24}
{"curie": "MONDO:0013556", "names": ["HPS4", "HERMANSKY-PUDLAK SYNDROME 4", "Hermansky-Pudlak syndrome 4", "HPS4 Hermansky-Pudlak syndrome", "Hermansky-Pudlak syndrome type 4", "Hermansky-Pudlak syndrome caused by mutation in HPS4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hermansky-Pudlak syndrome 4", "shortest_name_length": 4}
{"curie": "MONDO:0014445", "names": ["BBS17", "Bardet-Biedl syndrome 17", "BARDET-BIEDL SYNDROME 17", "LZTFL1 Bardet-Biedl syndrome", "Bardet-Biedl syndrome type 17", "Bardet-Biedl syndrome caused by mutation in LZTFL1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bardet-Biedl syndrome 17", "shortest_name_length": 5}
{"curie": "MONDO:0019849", "names": ["isolated micropenis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated micropenis", "shortest_name_length": 19}
{"curie": "MONDO:0019695", "names": ["acromelic dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acromelic dysplasia", "shortest_name_length": 19}
{"curie": "MONDO:0000369", "names": ["ABDOMEN TUBERCULOSIS", "abdominal tuberculosis", "Tuberculosis of abdomen", "tuberculosis of abdomen", "Tuberculosis of abdomen (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "abdominal tuberculosis", "shortest_name_length": 20}
{"curie": "MONDO:0027667", "names": ["efavirenz toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "efavirenz toxicity", "shortest_name_length": 18}
{"curie": "UMLS:C1135747", "names": ["Serogroup C Meningococcal Meningitis", "Meningococcal Meningitis, Serogroup C", "Meningitis, Meningococcal, Serogroup C"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meningitis, Meningococcal, Serogroup C", "shortest_name_length": 36}
{"curie": "UMLS:C0268222", "names": ["Fucosidosis type II", "Fucosidosis Type II", "Fucosidosis, type II", "Juvenile fucosidosis", "Juvenile Fucosidosis", "Childhood fucosidosis", "Fucosidosis, Juvenile", "Fucosidosis, juvenile form", "Juvenile fucosidosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fucosidosis Type II", "shortest_name_length": 19}
{"curie": "UMLS:C0151605", "names": ["Injection site edema", "Edema injection site", "EDEMA INJECTION SITE", "INJECTION SITE EDEMA", "Oedema injection site", "Injection site oedema", "injection site disorder edema", "Injection site edema (disorder)", "Injection site edema (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site edema", "shortest_name_length": 20}
{"curie": "MONDO:0017019", "names": ["ILD specific to infancy", "interstitial lung disease specific to infancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "interstitial lung disease specific to infancy", "shortest_name_length": 23}
{"curie": "MONDO:0002746", "names": ["fallopian tube adenocarcinoma", "Fallopian Tube Adenocarcinoma", "Adenocarcinoma of Fallopian Tube", "adenocarcinoma of fallopian tube", "Adenocarcinoma of the Fallopian Tube", "adenocarcinoma of the fallopian tube", "adenocarcinoma of fallopian tube (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fallopian tube adenocarcinoma", "shortest_name_length": 29}
{"curie": "UMLS:C0542313", "names": ["Somniloquy", "sleep talk", "Sleeptalking", "sleeptalking", "somniloquism", "Somniloquism", "sleep talking", "SLEEP TALKING", "Sleep Talking", "Sleep talking", "Talking, Sleep", "Sleeptalking (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sleep Talking", "shortest_name_length": 10}
{"curie": "MONDO:0014997", "names": ["NPHP20", "nephronophthisis 20", "NEPHRONOPHTHISIS 20", "nephronophthisis type 20", "MAPKBP1 nephronophthisis (disease)", "nephronophthisis (disease) caused by mutation in MAPKBP1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephronophthisis 20", "shortest_name_length": 6}
{"curie": "UMLS:C0750908", "names": ["Pre-Ictal Amnesia", "Amnesia, Pre-Ictal", "Amnesia, Pre Ictal", "Pre-Ictal Amnesias", "Amnesias, Pre-Ictal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pre-Ictal Amnesia", "shortest_name_length": 17}
{"curie": "MONDO:0001817", "names": ["Acute closed-angle glaucoma", "acute closed-angle glaucoma", "acute angle-closure glaucoma", "Acute angle-closure glaucoma", "Angle closure glaucoma acute", "acute angle closure glaucoma", "Acute angle closure glaucoma", "ANGLE CLOSURE GLAUCOMA ACUTE", "GLAUCOMA ACUTE ANGLE CLOSURE", "ACUTE ANGLE CLOSURE GLAUCOMA", "angle-closure glaucoma, acute", "AACG - Acute angle closure glaucoma", "Acute angle-closure glaucoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute closed-angle glaucoma", "shortest_name_length": 27}
{"curie": "UMLS:C0042035", "names": ["urination disorder", "Urination Disorder", "Urination disorders", "urination disorders", "disorder; urination", "Urination Disorders", "Disorder, Urination", "urination; disorder", "Micturition disorder", "micturition disorder", "MICTURITION DISORDER", "Disorders, Urination", "micturition; disorder", "disorder; micturition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urination Disorders", "shortest_name_length": 18}
{"curie": "MONDO:0018425", "names": ["C9ORF72-related Huntington disease phenocopy", "C9ORF72-related Huntington disease-like syndrome", "Huntington disease phenocopy due to C9ORF72 expansions", "Huntington disease-like syndrome due to C9ORF72 expansions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Huntington disease-like syndrome due to C9ORF72 expansions", "shortest_name_length": 44}
{"curie": "MONDO:0000943", "names": ["acute corneal hydrops", "acute hydrops of cornea", "Acute hydrops keratoconus", "acute hydrops keratoconus", "keratoconus, acute hydrops", "Keratoconus, acute hydrops", "Acute hydrops of the cornea", "Acute hydrops keratoconus (disorder)", "acute hydrops keratoconus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute hydrops keratoconus", "shortest_name_length": 21}
{"curie": "MONDO:0010989", "names": ["MURCS", "MRKH, type 2", "MRKH, Type II", "MRKH, TYPE II", "MURCS association", "MRKH syndrome type 2", "atypical MRKH syndrome", "Atypical MRKH syndrome", "Mayer-Rokitansky-Kuster-Hauser syndrome type 2", "Mayer-Rokitansky-Küster-Hauser syndrome type 2", "Mayer-Rokitansky-Kuster-Hauser syndrome, type 2", "Mayer-Rokitansky-Kuster-Hauser Syndrome, Type II", "MAYER-ROKITANSKY-KUSTER-HAUSER SYNDROME, TYPE II", "Atypical MRKH (Mayer Rokitansky Kuster Hauser) syndrome", "Mayer-Rokitansky-Küster-Hauser syndrome type 2 (disorder)", "KLIPPEL-FEIL DEFORMITY, CONDUCTIVE DEAFNESS, AND ABSENT VAGINA", "Klippel-Feil deformity, conductive deafness, and absent vagina", "Müllerian duct aplasia-renal dysplasia-cervical somite anomalies syndrome", "mullerian duct aplasia-renal dysplasia-cervical somite anomalies syndrome", "Mullerian duct aplasia-renal dysplasia-cervical somite anomalies syndrome", "Mullerian duct aplasia, renal dysplasia, cervical somite anomalies syndrome", "mullerian duct aplasia, unilateral renal aplasia, and cervicothoracic somite dysplasia", "Mullerian Duct Aplasia, Unilateral Renal Agenesis, And Cervicothoracic Somite Anomalies", "MULLERIAN duct aplasia, unilateral renal agenesis, and cervicothoracic somite anomalies", "MULLERIAN DUCT APLASIA, UNILATERAL RENAL AGENESIS, AND CERVICOTHORACIC SOMITE ANOMALIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mayer-Rokitansky-Küster-Hauser syndrome type 2", "shortest_name_length": 5}
{"curie": "MONDO:0007708", "names": ["KMP", "KMS", "KASABACH MERRIT SYNDROME", "Kasabach Merritt syndrome", "Kasabach Merritt Syndrome", "Kasabach-Merritt syndrome", "kasabach merritt syndrome", "kasabach-merritt syndrome", "Kasabach-Merritt Syndrome", "KASABACH-MERRITT SYNDROME", "Syndrome, Kasabach-Merritt", "Kasabach-Merritt Phenomenon", "Kasabach Merritt phenomenon", "Kasabach Merritt Phenomenon", "Phenomenon, Kasabach-Merritt", "Hemangioma-hemorrhage syndrome", "Hemangioma-Hemorrhage Syndrome", "hemangioma-hemorrhage syndrome", "THROMBOPENIA-HEMANGIOMA SYNDROME", "Haemangioma-haemorrhage syndrome", "thrombopenia-hemangioma syndrome", "Thrombopenia-Hemangioma Syndrome", "HEMANGIOMA-THROMBOCYTOPENIA SYNDROME", "Hemangioma Thrombocytopenia Syndrome", "Kasabach-Merritt syndrome (disorder)", "Thrombocytopenia Hemangioma Syndrome", "Thrombocytopenia-Hemangioma Syndrome", "hemangioma thrombocytopenia syndrome", "Thrombocytopenia-hemangioma syndrome", "Hemangioma-Thrombocytopenia Syndrome", "Hemangioma-thrombocytopenia syndrome", "thrombocytopenia-hemangioma syndrome", "hemangioma-thrombocytopenia syndrome", "Haemangioma-thrombocytopenia syndrome", "Thrombocytopenia-haemangioma syndrome", "Hemangioma Thrombocytopenia Syndromes", "Hemangiomatosis with Thrombocytopenia", "Syndrome, Hemangioma Thrombocytopenia", "hemangiomatosis with thrombocytopenia", "Hemangiomatosis with thrombocytopenia", "Thrombocytopenia-Hemangioma Syndromes", "Syndrome, Thrombocytopenia-Hemangioma", "Syndromes, Hemangioma Thrombocytopenia", "Haemangiomatosis with thrombocytopenia", "Syndromes, Thrombocytopenia-Hemangioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kasabach-Merritt syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C5556698", "names": ["Refractory Mucosal Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Mucosal Melanoma", "shortest_name_length": 27}
{"curie": "MONDO:0007122", "names": ["Anisocoria", "anisocoria", "ANISOCORIA", "anisocorias", "Pupil unequal", "unequal pupil", "pupils unequal", "unequal pupils", "Unequal pupils", "Pupils unequal", "Unequal pupil size", "Pupillary asymmetry", "anisocoria (disease)", "PUPILLARY INEQUALITY", "Anisocoria (disorder)", "Unequal pupil diameter", "anisocoria (diagnosis)", "Asymmetric pupil sizes", "Pupil Diameter Unequal", "Asymmetry of the pupils", "Unequal pupil dilatation", "Pupillary Size Inequality", "Inequality, Pupillary Size", "anisocoria (physical finding)", "Anisocoria - unequal pupil diameter", "anomalies of pupillary function anisocoria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anisocoria", "shortest_name_length": 10}
{"curie": "MONDO:0018620", "names": ["hypothalamic adipsic hypernatraemia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypothalamic adipsic hypernatraemia syndrome", "shortest_name_length": 44}
{"curie": "MONDO:0015755", "names": ["myopathy with hexagonally cross-linked tubular arrays", "Myopathy with hexagonally cross-linked tubular arrays", "Myopathy with hexagonally cross-linked tubular arrays (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy with hexagonally cross-linked tubular arrays", "shortest_name_length": 53}
{"curie": "UMLS:C5239080", "names": ["Unresectable Soft Tissue Leiomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Soft Tissue Leiomyosarcoma", "shortest_name_length": 39}
{"curie": "MONDO:0020739", "names": ["HCINF1", "Hypercalcemia, Infantile, 1", "HYPERCALCEMIA, INFANTILE, 1", "hypercalcemia, infantile, 1", "Idiopathic infantile hypercalcemia", "Idiopathic hypercalcemia of infancy", "Idiopathic infantile hypercalcaemia", "Idiopathic hypercalcaemia of infancy", "Hypercalcemia, Idiopathic, of Infancy", "HYPERCALCEMIA, IDIOPATHIC, OF INFANCY", "autosomal recessive infantile hypercalcemia 1", "Idiopathic hypercalcemia of infancy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypercalcemia, infantile, 1", "shortest_name_length": 6}
{"curie": "MONDO:0007207", "names": ["PHC Syndrome", "PHC syndrome", "PHC SYNDROME", "book syndrome", "BOOK SYNDROME", "Böök syndrome", "Book syndrome", "Book Syndrome", "Book's syndrome", "Book syndrome (disorder)", "Hyperhidrosis, premature cavities and premolar aplasia", "premolar aplasia, hyperhidrosis, and canities prematura"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Böök syndrome", "shortest_name_length": 12}
{"curie": "UMLS:C4744544", "names": ["Metastatic Vaginal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Vaginal Carcinoma", "shortest_name_length": 28}
{"curie": "UMLS:C3165106", "names": ["Invasive ductal carcinoma of female breast", "Infiltrating duct carcinoma of female breast", "Infiltrating ductal carcinoma of female breast", "Infiltrating duct carcinoma of female breast (disorder)", "Infiltrating ductal carcinoma of female breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infiltrating duct carcinoma of female breast", "shortest_name_length": 42}
{"curie": "MONDO:0013146", "names": ["ATFB16", "BRGDA7", "Brugada Syndrome 7", "BRUGADA SYNDROME 7", "Brugada syndrome 7", "SCN3B Brugada syndrome", "Brugada syndrome type 7", "Brugada syndrome 7 (diagnosis)", "atrial fibrillation, familial, 16", "ATRIAL FIBRILLATION, FAMILIAL, 16", "Brugada syndrome caused by mutation in SCN3B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brugada syndrome 7", "shortest_name_length": 6}
{"curie": "UMLS:C0206615", "names": ["Pneumovirus Infection", "Infection, Pneumovirus", "Pneumovirus Infections", "Infections, Pneumovirus", "Disease due to Pneumovirus", "DISEASES DUE TO PNEUMOVIRUS", "Disease caused by Pneumovirus", "Disease due to Pneumovirus, NOS", "Disease caused by Pneumovirus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pneumovirus Infections", "shortest_name_length": 21}
{"curie": "UMLS:C0280096", "names": ["adenocarcinoma CUP", "CUP, adenocarcinoma", "adenocarcinoma unknown primary", "ADENOCARCINOMA PRIMARY UNKNOWN", "adenocarcinoma primary unknown", "unknown primary, adenocarcinoma", "adenocarcinoma, unknown primary", "adenocarcinoma of unknown primary", "Adenocarcinoma of Unknown Primary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma of Unknown Primary", "shortest_name_length": 18}
{"curie": "UMLS:C5555187", "names": ["Refractory Primary Peritoneal Endometrioid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Primary Peritoneal Endometrioid Adenocarcinoma", "shortest_name_length": 57}
{"curie": "UMLS:C0392441", "names": ["En coup de sabre", "en coup de sabre", "coup de en sabre", "En coup de sabre lesion", "en coup de sabre lesion", "lesion; en coup de sabre", "en coup de sabre; lesion", "Morphea en coup de sabre", "Morphoea en coup de sabre", "Coup de sabre scleroderma", "Frontal Linear Scleroderma", "Scleroderma en Coup de Sabre", "en coup de sabre; scleroderma", "scleroderma; en coup de sabre", "Coup de sabre scleroderma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Coup de sabre scleroderma", "shortest_name_length": 16}
{"curie": "MONDO:0004168", "names": ["cribriform variant testicular seminoma", "Testicular Seminoma, Cribriform Variant", "testicular seminoma, cribriform variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cribriform variant testicular seminoma", "shortest_name_length": 38}
{"curie": "UMLS:C0600076", "names": ["sticker tumor", "Infective granuloma", "Infectious Granuloma", "infectious granuloma", "Infectious granuloma", "infectious; granuloma", "granuloma; infectious", "Infectious granuloma (disorder)", "Infective granuloma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infectious granuloma", "shortest_name_length": 13}
{"curie": "MONDO:0030503", "names": ["PFIC7", "CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 7, WITH OR WITHOUT HEARING LOSS", "cholestasis, progressive familial intrahepatic, 7, with or without hearing loss"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholestasis, progressive familial intrahepatic, 7, with or without hearing loss", "shortest_name_length": 5}
{"curie": "MONDO:0044300", "names": ["FAP4", "MSH3-related AFAP", "MSH3-related attenuated FAP", "familial adenomatous polyposis 4", "FAMILIAL ADENOMATOUS POLYPOSIS 4", "familial adenomatous polyposis type 4", "MSH3-related attenuated familial polyposis coli", "MSH3-related attenuated familial adenomatous polyposis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial adenomatous polyposis 4", "shortest_name_length": 4}
{"curie": "UMLS:C5208293", "names": ["Urinary tract candidiasis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urinary tract candidiasis", "shortest_name_length": 25}
{"curie": "MONDO:0004560", "names": ["Follicular infundibulum tumor", "Follicular Infundibulum Tumor", "follicular infundibulum tumor", "Follicular infundibulum tumour", "follicular infundibulum tumour", "Tumor of follicular infundibulum", "Follicular Infundibulum Neoplasm", "follicular infundibulum neoplasm", "tumor of follicular infundibulum", "Tumour of follicular infundibulum", "tumour of follicular infundibulum", "Tumor of the Follicular Infundibulum", "tumor of the follicular infundibulum", "Neoplasm of the Follicular Infundibulum", "Benign tumor of follicular infundibulum", "neoplasm of the Follicular Infundibulum", "neoplasm of the follicular infundibulum", "Benign tumour of follicular infundibulum", "Tumor of follicular infundibulum (disorder)", "basal cell hamartoma with follicular differentiation", "Basal cell hamartoma with follicular differentiation", "Basal Cell Hamartoma with Follicular Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "follicular infundibulum tumor", "shortest_name_length": 29}
{"curie": "UMLS:C3273071", "names": ["Bile Duct Mucinous Cystic Neoplasm, High-Grade", "Bile Duct Mucinous Cystic Neoplasm, High Grade", "Bile Duct MCN with High Grade Intraepithelial Neoplasia", "Bile Duct Mucinous Cystic Neoplasm with High Grade Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bile Duct Mucinous Cystic Neoplasm, High Grade", "shortest_name_length": 46}
{"curie": "MONDO:0019071", "names": ["HNED", "PHNED", "hair-nail ectodermal dysplasia", "pure hair and nail ectodermal dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pure hair and nail ectodermal dysplasia", "shortest_name_length": 4}
{"curie": "MONDO:0700094", "names": ["unbalanced Robertsonian translocation Down syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "unbalanced Robertsonian translocation Down syndrome", "shortest_name_length": 51}
{"curie": "UMLS:C0751124", "names": ["Atypical absence epilepsy", "epilepsy atypical absence", "Epilepsy, Absence, Atypical", "Atypical absence epilepsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epilepsy, Absence, Atypical", "shortest_name_length": 25}
{"curie": "UMLS:C1707589", "names": ["Cutaneous B Lymphoblastic Leukemia/Lymphoma", "Cutaneous B-Lymphoblastic Leukemia/Lymphoma", "Cutaneous Precursor B-Lymphoblastic Lymphoma/Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous B Lymphoblastic Leukemia/Lymphoma", "shortest_name_length": 43}
{"curie": "UMLS:C0877400", "names": ["vertebral lesion", "Vertebral lesion", "lesions vertebral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vertebral lesion", "shortest_name_length": 16}
{"curie": "UMLS:C4683738", "names": ["Mycosis Fungoides and Sezary Syndrome by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mycosis Fungoides and Sezary Syndrome by AJCC v8 Stage", "shortest_name_length": 54}
{"curie": "MONDO:0006933", "names": ["Histiocytoma of lung", "lung inflammatory pseudotumor", "Plasma cell granuloma of lung", "inflammatory lung pseudotumor", "Plasma Cell Granuloma of Lung", "inflammatory lung pseudotumour", "Pulmonary plasma cell granuloma", "pulmonary plasma cell granuloma", "Pulmonary Plasma Cell Granuloma", "lymphocytic pseudotumor of lung", "Histiocytoma of lung (disorder)", "Lymphocytic pseudotumor of lung", "Inflammatory pseudotumor of lung", "Histiocytoma of lung (diagnosis)", "Inflammatory Pseudotumor of Lung", "Plasma Cell Granuloma, Pulmonary", "Lymphocytic pseudotumour of lung", "Pulmonary Granuloma, Plasma Cell", "Granuloma, Plasma Cell, Pulmonary", "granuloma, plasma cell, pulmonary", "Inflammatory pseudotumour of lung", "Sclerosing hemangiocytoma of lung", "sclerosing hemangiocytoma of lung", "Pulmonary Inflammatory Pseudotumor", "Sclerosing haemangiocytoma of lung", "Inflammatory Pulmonary Pseudotumor", "Pulmonary Inflammatory Pseudotumors", "Pulmonary Pseudotumor, Inflammatory", "Inflammatory Pulmonary Pseudotumors", "Inflammatory Pseudotumor, Pulmonary", "Pseudotumor, Pulmonary Inflammatory", "Pulmonary Pseudotumors, Inflammatory", "Pseudotumor, Inflammatory, Pulmonary", "benign neoplasm histiocytoma of lung", "Inflammatory Pseudotumors, Pulmonary", "Plasma cell granuloma of lung (disorder)", "Lymphocytic pseudotumor of lung (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary plasma cell granuloma", "shortest_name_length": 20}
{"curie": "MONDO:0009855", "names": ["DBP deficiency", "DBP DEFICIENCY", "PBFE DEFICIENCY", "Pbfe deficiency", "HSD17B4 deficiency", "Pseudo-Zellweger Syndrome", "pseudo-Zellweger syndrome", "Pseudo-Zellweger syndrome", "Bifunctional enzyme deficiency", "bifunctional enzyme deficiency", "Peroxisomal thiolase deficiency", "D-Bifunctional Enzyme Deficiency", "D-bifunctional enzyme deficiency", "D-bifunctional protein deficiency", "D-BIFUNCTIONAL PROTEIN DEFICIENCY", "d-bifunctional protein deficiency", "Multifunctional Enzyme Deficiency", "D-Bifunctional Protein Deficiency", "multifunctional enzyme deficiency", "3-Ketoacyl-CoA thiolase deficiency", "Pseudo Zellweger syndrome leukodystrophy", "peroxisomal bifunctional enzyme deficiency", "Peroxisomal bifunctional enzyme deficiency", "PEROXISOMAL BIFUNCTIONAL ENZYME DEFICIENCY", "Bifunctional peroxisomal enzyme deficiency", "Peroxisomal thiolase deficiency (disorder)", "peroxisomal multifunctional enzyme deficiency", "Peroxisomal Multifunctional Enzyme Deficiency", "17-beta-hydroxysteroid dehydrogenase 4 deficiency", "17-beta-hydroxysteroid dehydrogenase IV deficiency", "17-BETA-HYDROXYSTEROID DEHYDROGENASE IV DEFICIENCY", "Peroxisomal bifunctional enzyme complex deficiency", "Peroxisomal Multifunctional Enzyme (MFE2) Deficiency", "peroxisomal multifunctional enzyme (MFE2) deficiency", "17-beta-hydroxysteroid dehydrogenase 4, deficiency of", "Bifunctional peroxisomal enzyme deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "d-bifunctional protein deficiency", "shortest_name_length": 14}
{"curie": "UMLS:C0677683", "names": ["Stage I Mantle Cell Lymphoma", "mantle cell lymphoma stage I", "stage I mantle cell lymphoma", "Mantle Cell Lymphoma Stage I", "Mantle cell lymphoma stage I", "Ann Arbor Stage I Mantle Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mantle cell lymphoma stage I", "shortest_name_length": 28}
{"curie": "MONDO:0013912", "names": ["HH10", "TAC3 hypogonadotropic hypogonadism", "hypogonadotropic hypogonadism 10 with or without anosmia", "HYPOGONADOTROPIC HYPOGONADISM 10 WITH OR WITHOUT ANOSMIA", "hypogonadotropic hypogonadism caused by mutation in TAC3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadotropic hypogonadism 10 with or without anosmia", "shortest_name_length": 4}
{"curie": "MONDO:0014680", "names": ["IIAE7", "IRF3 herpes simplex encephalitis", "Herpes simplex encephalitis, susceptibility to, 5", "herpes simplex encephalitis, susceptibility to, 7", "HERPES SIMPLEX ENCEPHALITIS, SUSCEPTIBILITY TO, 5", "Herpes simplex encephalitis, susceptibility to, type 7", "herpes simplex encephalitis caused by mutation in IRF3", "encephalopathy, acute, infection-induced, susceptibility to, 7", "ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 7", "encephalopathy, acute, infection-induced (Herpes-specific), susceptibility to, 7", "encephalopathy, acute, infection-induced (HERPES-specific), susceptibility to, 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "herpes simplex encephalitis, susceptibility to, 7", "shortest_name_length": 5}
{"curie": "MONDO:0800103", "names": ["COACH1", "COACH SYNDROME 1", "COACH syndrome 1", "cerebellar vermis hypo/aplasia, oligophrenia, congenital ataxia, ocular coloboma, and hepatic fibrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "COACH syndrome 1", "shortest_name_length": 6}
{"curie": "UMLS:C0278505", "names": ["stage II NSCLC", "NSCLC, stage II", "stage II nonsmall cell lung cancer", "non-oat cell lung cancer, stage II", "Non-small cell lung cancer stage II", "nonsmall cell lung cancer, stage II", "stage II non-small cell lung cancer", "lung cancer, non-oat cell, stage II", "Lung cancer non-small cell stage II", "Non Small Cell Lung Cancer Stage II", "Stage II Non-Small Cell Lung Cancer", "non-small cell lung cancer, stage II", "Stage II Non-Oat Cell Lung Carcinoma", "Non -Small Cell Lung Cancer Stage II", "lung cancer, nonsmall cell, stage II", "Stage II Non-Small Cell Lung Carcinoma", "Stage II Non-Oat Cell Carcinoma of Lung", "Stage II Non-Small Cell Carcinoma of Lung", "Stage II Non-Oat Cell Carcinoma of the Lung", "Stage II Lung Non-Small Cell Cancer AJCC v7", "Stage II Non-Small Cell Lung Cancer AJCC v7", "Stage II Non-Small Cell Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-small cell lung cancer stage II", "shortest_name_length": 14}
{"curie": "UMLS:C0854969", "names": ["Prostate cancer stage 0", "Prostatic cancer stage 0"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate cancer stage 0", "shortest_name_length": 23}
{"curie": "UMLS:C5239077", "names": ["Unresectable Round Cell Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Round Cell Liposarcoma", "shortest_name_length": 35}
{"curie": "MONDO:0003307", "names": ["multiple mucosal neuroma", "Multiple mucosal neuromas", "Multiple Mucosal Neuromas", "multiple mucosal neuromas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple mucosal neuroma", "shortest_name_length": 24}
{"curie": "MONDO:0015571", "names": ["Del (5)(q35)", "Deletion 5q35", "deletion 5q35", "Del (5)(qter)", "Monosomy 5q35", "monosomy 5q35", "Distal 5q deletion", "deletion type 5q35", "distal 5q deletion", "telomeric deletion 5q", "Telomeric deletion 5q", "Deletion 5q35 (disorder)", "Chromosome 5, monosomy 5q35"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deletion 5q35", "shortest_name_length": 12}
{"curie": "MONDO:0060760", "names": ["IDDFBA", "INTELLECTUAL developmental disorder with DYSMORPHIC facies and behavioral abnormalities", "intellectual developmental disorder with dysmorphic facies and behavioral abnormalities", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder with dysmorphic facies and behavioral abnormalities", "shortest_name_length": 6}
{"curie": "MONDO:0021576", "names": ["Fallopian Tube Endometrioid Tumor", "fallopian tube endometrioid tumor", "fallopian tube endometrium neoplasm", "Fallopian Tube Endometrioid Neoplasm", "fallopian tube endometrioid neoplasm", "endometrium neoplasm of fallopian tube"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fallopian tube endometrioid tumor", "shortest_name_length": 33}
{"curie": "UMLS:C0877661", "names": ["Application site burn", "Application site burning", "Application site thermal burn", "Application site burn (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Application site burn", "shortest_name_length": 21}
{"curie": "MONDO:0001060", "names": ["EGC", "early gastric cancer", "Early Gastric Cancer", "Early gastric cancer", "Surface gastric cancer", "surface gastric cancer", "Surface Gastric Cancer", "superficial gastric cancer", "Superficial Gastric Cancer", "EGC - Early gastric cancer", "Microinvasive Gastric Cancer", "microinvasive gastric cancer", "Early gastric cancer (disorder)", "Early gastric cancer (diagnosis)", "superficial spreading gastric cancer", "Superficial Spreading Gastric Cancer", "gastric neoplasm malignant early cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microinvasive gastric cancer", "shortest_name_length": 3}
{"curie": "MONDO:0018516", "names": ["anal canal epithelial neoplasm", "epithelial tumor of anal canal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epithelial tumor of anal canal", "shortest_name_length": 30}
{"curie": "MONDO:0014526", "names": ["PGBM2", "polyglucosan body myopathy 2", "POLYGLUCOSAN BODY MYOPATHY 2", "GYG1 polyglucosan body myopathy", "Polyglucosan body myopathy type 2", "polyglucosan body myopathy type 2", "PGBM2 - polyglucosan body myopathy type 2", "Polyglucosan body myopathy type 2 (disorder)", "polyglucosan body myopathy caused by mutation in GYG1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyglucosan body myopathy type 2", "shortest_name_length": 5}
{"curie": "MONDO:0014845", "names": ["SCAR22", "VWA3B autosomal recessive cerebellar ataxia", "autosomal recessive spinocerebellar ataxia 22", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 22", "spinocerebellar ataxia, autosomal recessive 22", "spinocerebellar ataxia, autosomal recessive type 22", "spinocerebellar ataxia, autosomal recessive 22; SCAR22", "autosomal recessive cerebellar ataxia caused by mutation in VWA3B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia, autosomal recessive 22", "shortest_name_length": 6}
{"curie": "UMLS:C4526591", "names": ["Stage IV Thymus Epithelial Neoplasm", "Stage IV Thymus Epithelial Neoplasm AJCC v8", "Stage IV Thymic Epithelial Neoplasm AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Thymic Epithelial Neoplasm AJCC v8", "shortest_name_length": 35}
{"curie": "MONDO:0001862", "names": ["malignant visceral pleura tumor", "Malignant neoplasm of visceral pleura", "Primary malignant neoplasm of visceral pleura", "primary malignant neoplasm of visceral pleura", "lung neoplasm malignant visceral pleura primary", "Primary malignant neoplasm of visceral pleura (disorder)", "Primary malignant neoplasm of visceral pleura (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant visceral pleura tumor", "shortest_name_length": 31}
{"curie": "UMLS:C0854960", "names": ["stage I vulva cancer", "stage I vulvar cancer", "Vulval cancer stage I", "Stage I Vulvar Cancer", "vulva cancer, stage I", "vulvar cancer, stage I", "Stage I Vulvar Carcinoma", "stage I cancer of the vulva", "cancer of the vulva, stage I", "Stage I Vulva Cancer AJCC v6", "Stage I Vulval Cancer AJCC v6", "Vulvar Cancer Stage I AJCC v6", "Stage I Vulvar Cancer AJCC v6", "stage I carcinoma of the vulva", "carcinoma of the vulva, stage I", "Stage I Vulval Carcinoma AJCC v6", "Stage I Vulvar Carcinoma AJCC v6", "AJCC Stage I Vulvar Cancer AJCC v6", "FIGO Stage I Vulva Carcinoma AJCC v6", "FIGO Stage I Vulvar Carcinoma AJCC v6", "FIGO Stage I Carcinoma of Vulva AJCC v6", "FIGO Stage I Carcinoma of the Vulva AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Vulvar Carcinoma", "shortest_name_length": 20}
{"curie": "MONDO:0008232", "names": ["phagocytosis, plasma-RELATED defect IN", "PHAGOCYTOSIS, PLASMA-RELATED DEFECT IN", "Phagocytosis, Plasma-Related Defect in", "phagocytosis, plasma-related defect 1N", "phagocytosis, plasma-related defect type 1N"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phagocytosis, plasma-related defect 1N", "shortest_name_length": 38}
{"curie": "MONDO:0012269", "names": ["Del(3)(q29)", "Monosomy 3q29", "3q29 deletion", "monosomy 3q29", "Monosomy 3qter", "3qter deletion", "monosomy 3qter", "3q29 deletion syndrome", "3q29 recurrent deletion", "MICRODELETION 3q29 SYNDROME", "microdeletion 3Q29 syndrome", "3q29 microdeletion syndrome", "Microdeletion 3q29 Syndrome", "3q subtelomere deletion syndrome", "Chromosome 3q29 Deletion Syndrome", "chromosome 3q29 deletion syndrome", "CHROMOSOME 3q29 DELETION SYNDROME", "chromosome 3q29 microdeletion syndrome", "3q29 microdeletion syndrome (disorder)", "chromosome 3q29 microdeletion syndrome, isolated cases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 3q29 microdeletion syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0018268", "names": ["Medich macrothrombocytopenia", "Medich giant platelet syndrome", "Medich giant platelet syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Medich giant platelet syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0012766", "names": ["SPG37", "hereditary spastic paraplegia 37", "hereditary spastic paraplegia type 37", "autosomal dominant spastic paraplegia 37", "SPASTIC PARAPLEGIA 37, AUTOSOMAL DOMINANT", "spastic paraplegia 37, autosomal dominant", "Spastic Paraplegia 37, Autosomal Dominant", "autosomal dominant spastic paraplegia type 37", "Autosomal dominant spastic paraplegia type 37", "familial spastic paraplegia autosomal dominant type 37", "Autosomal dominant spastic paraplegia type 37 (disorder)", "Autosomal dominant spastic paraplegia type 37 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 37", "shortest_name_length": 5}
{"curie": "MONDO:0018237", "names": ["Acrofacial Dysostosis", "acrofacial dysostosis", "Acrofacial dysostosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acrofacial dysostosis", "shortest_name_length": 21}
{"curie": "MONDO:0004317", "names": ["Multiple Intraspinal Meningiomas", "multiple intraspinal Meningiomas", "multiple spinal canal and spinal cord meningioma", "multiple spinal canal and spinal cord Meningiomas", "Multiple Spinal Canal and Spinal Cord Meningiomas", "multiple Meningiomas of spinal canal and spinal cord", "Multiple Meningiomas of Spinal Canal and Spinal Cord", "Multiple Meningiomas of the Spinal Canal and Spinal Cord", "Multiple meningiomas of the Spinal canal and Spinal Cord", "multiple meningiomas of the spinal canal and spinal cord"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple spinal canal and spinal cord meningioma", "shortest_name_length": 32}
{"curie": "UMLS:C1707508", "names": ["Conventional Dermatofibrosarcoma Protuberans"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conventional Dermatofibrosarcoma Protuberans", "shortest_name_length": 44}
{"curie": "MONDO:0024542", "names": ["DES", "CAMRQ1", "Chmrq1", "Vldlrch", "Vldlr-Ch", "Des-Vldlr", "dysequilibrium syndrome", "Dysequilibrium syndrome", "DYSEQUILIBRIUM SYNDROME", "VLDLR dysequilibrium syndrome", "Dysequilibrium Syndrome-Vldlr", "Vldlr-Associated Cerebellar Hypoplasia", "Cerebellar Hypoplasia, VLDLR-Associated", "cerebellar hypoplasia, VLDLR-associated", "Cerebellar hypoplasia, VLDLR associated", "CEREBELLAR HYPOPLASIA, VLDLR-ASSOCIATED", "dysequilibrium syndrome caused by mutation in VLDLR", "Cerebellar disorder, nonprogressive, with mental retardation", "Autosomal Recessive Cerebellar Ataxia with Mental Retardation", "CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 1", "cerebellar ataxia, mental retardation, and dysequilibrium syndrome 1", "Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 1", "cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 1", "cerebellar ataxia, mental retardation, and dysequilibrium syndrome type 1", "Cerebellar Ataxia, Congenital, And Mental Retardation, Autosomal Recessive", "cerebellar ataxia, congenital, and mental retardation, autosomal recessive", "CEREBELLAR ATAXIA, CONGENITAL, AND MENTAL RETARDATION, AUTOSOMAL RECESSIVE", "Autosomal Recessive Cerebellar Hypoplasia with Cerebral Gyral Simplification", "cerebellar ataxia, intellectual disability, and dysequilibrium syndrome type 1", "cerebellar ataxia, congenital, and intellectual disability, autosomal recessive", "CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDAL LOCOMOTION 1", "cerebellar ataxia and mental retardation with or without quadrupedal locomotion 1", "Cerebellar Hypoplasia and Mental Retardation with Or without Quadrupedal Locomotion", "CEREBELLAR ATAXIA, IMPAIRED INTELLECTUAL DEVELOPMENT, AND DYSEQUILIBRIUM SYNDROME 1", "cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1", "CEREBELLAR ATAXIA, INTELLECTUAL DEVELOPMENTAL DISORDER, AND DYSEQUILIBRIUM SYNDROME 1", "cerebellar ataxia and intellectual disability with or without quadrupedal locomotion 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 1", "shortest_name_length": 3}
{"curie": "UMLS:C3661519", "names": ["Hereditary Motor Neuronopathy", "Neuronopathy, Hereditary Motor", "Motor Neuronopathy, Hereditary", "Hereditary Motor Neuronopathies", "Motor Neuronopathies, Hereditary", "Neuronopathies, Hereditary Motor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hereditary Motor Neuronopathy", "shortest_name_length": 29}
{"curie": "MONDO:0010154", "names": ["trigonocephaly - bifid nose - acral anomalies", "trigonocephaly-bifid nose-acral anomalies syndrome", "Trigonobrachycephaly, Bulbous Bifid Nose, Micrognathia, and Abnormalities of the Hands and Feet", "TRIGONOBRACHYCEPHALY, BULBOUS BIFID NOSE, MICROGNATHIA, AND ABNORMALITIES OF THE HANDS AND FEET", "trigonobrachycephaly, bulbous bifid nose, micrognathia, and abnormalities of the hands and feet", "trigonobrachycephaly, bulbous bifid nose, macrostomia, micrognathia, acral anomalies, and hypotonia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trigonocephaly-bifid nose-acral anomalies syndrome", "shortest_name_length": 45}
{"curie": "MONDO:0002198", "names": ["vulvar glandular tumor", "Vulvar Glandular Tumor", "vulvar glandular neoplasm", "Vulvar Glandular Neoplasm", "mammalian vulva glandular cell neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar glandular neoplasm", "shortest_name_length": 22}
{"curie": "MONDO:0034110", "names": ["atypical Fanconi syndrome-neonatal hyperinsulinism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical Fanconi syndrome-neonatal hyperinsulinism syndrome", "shortest_name_length": 59}
{"curie": "MONDO:0019652", "names": ["familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation", "shortest_name_length": 93}
{"curie": "MONDO:0016639", "names": ["Fried-Goldberg-Mundel syndrome", "Fried Goldberg Mundel syndrome", "lower limb deficiency-hypospadias syndrome", "lower limb malformation-hypospadias syndrome", "Lower limb malformation hypospadias syndrome", "Lower limb malformation-hypospadias syndrome", "Lower limb malformation hypospadias syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lower limb deficiency-hypospadias syndrome", "shortest_name_length": 30}
{"curie": "MONDO:0700096", "names": ["human disease", "human disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "human disease", "shortest_name_length": 13}
{"curie": "UMLS:C0018566", "names": ["MALFORMATION HAND", "malformation hand", "hand malformation", "congenital hand deformity", "congenital deformity hand", "Congenital Hand Deformity", "HAND DEFORMITY CONGENITAL", "Deformity, Congenital Hand", "Hand Deformity, Congenital", "congenital deformities hand", "Congenital Hand Deformities", "deformity; hand, congenital", "congenital hand deformities", "hand; deformity, congenital", "Hand Deformities, Congenital", "Congenital hand malformation", "Congenital deformity of hand", "Deformities, Congenital Hand", "congenital hand malformations", "Congenital hand malformation NOS", "congenital hand deformity (diagnosis)", "Congenital deformity of hand (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Hand Deformities", "shortest_name_length": 17}
{"curie": "UMLS:C5557348", "names": ["HPV-Independent Vulvar Squamous Cell Carcinoma", "Human Papillomavirus-Independent Vulvar Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Human Papillomavirus-Independent Vulvar Squamous Cell Carcinoma", "shortest_name_length": 46}
{"curie": "UMLS:C1336492", "names": ["Ureter Cancer Stage I", "Stage I Ureter Cancer", "Stage I Ureter Carcinoma", "Stage I Ureteral Carcinoma", "Stage I Carcinoma of Ureter", "Stage I Ureter Cancer AJCC v7", "Stage I Carcinoma of the Ureter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Ureter Cancer AJCC v7", "shortest_name_length": 21}
{"curie": "MONDO:0002271", "names": ["COAD", "adenocarcinoma colon", "colon adenocarcinoma", "Colon Adenocarcinoma", "COLON ADENOCARCINOMA", "Adenocarcinoma, Colon", "Colon Adenocarcinomas", "Colonic Adenocarcinoma", "Colonic adenocarcinoma", "colonic adenocarcinoma", "Adenocarcinomas, Colon", "Adenocarcinoma - colon", "adenocarcinoma - colon", "Adenocarcinoma of Colon", "adenocarcinoma of colon", "Adenocarcinoma of colon", "adenocarcinoma colon cancer", "Adenocarcinoma of the Colon", "adenocarcinoma of the colon", "Adenocarcinoma of the colon", "colon cancer adenocarcinoma", "colon cancer, adenocarcinoma", "colon, adenocarcinoma of the", "COLON NOS CANCER ADENOCARCINOMA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colon adenocarcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0007048", "names": ["AKV", "AKV of Hopf", "Hopf disease", "HOPF DISEASE", "Hopf Disease", "Disease, Hopf", "Hopf Diseases", "Diseases, Hopf", "Acrokeratosis Verruciformis", "acrokeratosis verruciformis", "Acrokeratosis verruciformis", "ACROKERATOSIS VERRUCIFORMIS", "Verruciformis, Acrokeratosis", "Hopf Acrokeratosis Verruciformis", "AKV - Acrokeratosis verruciformis", "Acrokeratosis verruciformis of Hopf", "acrokeratosis verruciformis of Hopf", "Acrokeratosis Verruciformis of Hopf", "Acrokeratosis verruciformis of Hopf (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acrokeratosis verruciformis", "shortest_name_length": 3}
{"curie": "UMLS:C0346770", "names": ["Malignant Skin Adnexal Tumor", "Malignant Skin Adnexal Neoplasm", "Malignant Skin Appendage Neoplasm", "Malignant Epidermal Appendage Tumor", "Malignant Cutaneous Adnexal Neoplasm", "Malignant Epidermal Appendage Neoplasm", "Malignant Tumor of Epidermal Appendage", "Malignant tumor of epidermal appendage", "Malignant tumour of epidermal appendage", "Malignant Neoplasm of Epidermal Appendage", "Malignant Tumor of the Epidermal Appendage", "Malignant Neoplasm of the Epidermal Appendage", "Malignant skin tumor with adnexal differentiation", "Malignant skin tumour with adnexal differentiation", "Malignant skin tumor with adnexal differentiation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant tumor of epidermal appendage", "shortest_name_length": 28}
{"curie": "UMLS:C0334058", "names": ["Mild epithelial dysplasia", "Mild Epithelial Dysplasia", "mild epithelial dysplasia", "Grade 1 Intraepithelial Neoplasia", "Grade I Intraepithelial Neoplasia", "Low Grade Intraepithelial Neoplasia", "Mild epithelial dysplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mild epithelial dysplasia", "shortest_name_length": 25}
{"curie": "UMLS:C4086158", "names": ["Ganglioneuroblastoma", "Childhood Ganglioneuroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Ganglioneuroblastoma", "shortest_name_length": 20}
{"curie": "UMLS:C4329963", "names": ["Factor I Inactivation", "Factor I Inhibitor Present"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Factor I Inactivation", "shortest_name_length": 21}
{"curie": "MONDO:0009709", "names": ["CNM2", "AR-CNM", "centronuclear myopathy 2", "MYOPATHY, CENTRONUCLEAR, 2", "myopathy, centronuclear, 2", "BIN1 centronuclear myopathy", "myopathy, centronuclear, type 2", "MYOTUBULAR MYOPATHY, AUTOSOMAL RECESSIVE", "Myotubular Myopathy, Autosomal Recessive", "myotubular myopathy, autosomal recessive", "Autosomal recessive centronuclear myopathy", "MYOPATHY, CENTRONUCLEAR, AUTOSOMAL RECESSIVE", "myopathy, centronuclear, autosomal recessive", "Myopathy, Centronuclear, Autosomal Recessive", "centronuclear myopathy caused by mutation in BIN1", "Autosomal recessive centronuclear myopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy, centronuclear, 2", "shortest_name_length": 4}
{"curie": "UMLS:C0271278", "names": ["krukenberg spindle", "Krukenberg spindle", "spindle; Krukenberg", "Krukenberg; spindle", "krukenberg spindles", "Krukenberg's spindle", "spindle, Krukenberg's", "Krukenberg spindle (finding)", "Krukenberg spindle (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Krukenberg spindle", "shortest_name_length": 18}
{"curie": "MONDO:0007868", "names": ["Sthe", "HKPX1", "Kok disease", "HYPEREKPLEXIA 1", "hyperekplexia 1", "Stiff-baby syndrome", "hyperekplexia type 1", "startle disease, familial", "hyperekplexia, hereditary 1", "exaggerated startle reaction", "startle reaction, exaggerated", "Stiff-Man syndrome, congenital", "hyperekplexia, hereditary type 1", "Stiff-Person syndrome, congenital"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperekplexia 1", "shortest_name_length": 4}
{"curie": "MONDO:0025556", "names": ["Isocyanate induced asthma", "isocyanate induced asthma", "isocyanates allergic asthma", "Isocyanate induced asthma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isocyanate induced asthma", "shortest_name_length": 25}
{"curie": "UMLS:C1333095", "names": ["Colon Mantle Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colon Mantle Cell Lymphoma", "shortest_name_length": 26}
{"curie": "MONDO:0019831", "names": ["congenital anomaly of the coronary sinus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital anomaly of the coronary sinus", "shortest_name_length": 40}
{"curie": "UMLS:C0153888", "names": ["CML in Remission", "Chronic Myeloid Leukemia in Remission", "Chronic myeloid leukemia in remission", "Chronic myeloid leukemia, in remission", "Chronic myeloid leukaemia in remission", "Chronic myeloid leukemia (in remission)", "Chronic myeloid leukaemia, in remission", "Chronic Myeloid Leukemia (in Remission)", "Chronic Myelocytic Leukemia in Remission", "Chronic myeloid leukaemia (in remission)", "chronic myelogenous leukemia in remission", "Chronic Myelogenous Leukemia in Remission", "Chronic Granulocytic Leukemia in Remission", "Chronic Myelogenous Leukemia (CML) in Remission", "CML (chronic myelogenous leukemia) in remission", "Chronic myeloid leukemia in remission (disorder)", "chronic myelogenous leukemia in remission (diagnosis)", "Chronic Myelogenous Leukemia, BCR-ABL1 Positive in Remission"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic myeloid leukemia in remission", "shortest_name_length": 16}
{"curie": "UMLS:C0751603", "names": ["Autosomal recessive hereditary spastic paraplegia", "Autosomal Recessive Hereditary Spastic Paraplegia", "Hereditary Autosomal Recessive Spastic Paraplegia", "Autosomal Recessive Spastic Paraplegia, Hereditary", "Hereditary Spastic Paraplegia, Autosomal Recessive", "Spastic Paraplegia, Autosomal Recessive, Hereditary", "Spastic Paraplegia, Hereditary, Autosomal Recessive", "Autosomal recessive hereditary spastic paraplegia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Autosomal Recessive Hereditary Spastic Paraplegia", "shortest_name_length": 49}
{"curie": "MONDO:0003931", "names": ["childhood optic tract astrocytoma", "pediatric optic tract astrocytoma", "pediatric visual pathway astrocytoma", "Childhood Visual Pathway Astrocytoma", "optic tract astrocytoma of childhood", "Pediatric Visual Pathway Astrocytoma", "childhood visual pathway astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood optic tract astrocytoma", "shortest_name_length": 33}
{"curie": "MONDO:0015785", "names": ["Prader-Willi syndrome due to translocation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prader-Willi syndrome due to translocation", "shortest_name_length": 42}
{"curie": "MONDO:0012925", "names": ["DBA5", "Dba5", "Diamond-Blackfan Anemia 5", "DIAMOND-BLACKFAN ANEMIA 5", "Diamond-Blackfan anemia 5", "Diamond-Blackfan Anemia type 5", "RPL35A Diamond-Blackfan anemia", "RPL35A-related Diamond-Blackfan anemia", "Diamond-Blackfan anemia caused by mutation in RPL35A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diamond-Blackfan anemia 5", "shortest_name_length": 4}
{"curie": "MONDO:0001784", "names": ["malignant renal hypertension", "malignant renal artery stenosis", "malignant renovascular hypertension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant renovascular hypertension", "shortest_name_length": 28}
{"curie": "MONDO:0018807", "names": ["IAD", "idiopathic ductopenia", "idiopathic adult ductopenia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic ductopenia", "shortest_name_length": 3}
{"curie": "MONDO:0003195", "names": ["peritoneum serous adenocarcinoma", "peritoneal serous adenocarcinoma", "primary peritoneal serous adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peritoneal serous adenocarcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C5235862", "names": ["Unresectable Thyroid Gland Medullary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Thyroid Gland Medullary Carcinoma", "shortest_name_length": 46}
{"curie": "MONDO:0013356", "names": ["VUR3", "VESICOURETERAL REFLUX 3", "vesicoureteral reflux 3", "vesicoureteral reflux type 3", "SOX17 vesicoureteral reflux (disease)", "vesicoureteral reflux (disease) caused by mutation in SOX17"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vesicoureteral reflux 3", "shortest_name_length": 4}
{"curie": "MONDO:0016292", "names": ["Nodular heterotopia", "nodular heterotopia", "genetic nodular heterotopia", "nodular neuronal heterotopia", "Nodular heterotopia (disorder)", "hereditary nodular heterotopia", "nodular heterotopia (diagnosis)", "congenital malformation brain nodular heterotopia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nodular neuronal heterotopia", "shortest_name_length": 19}
{"curie": "UMLS:C0153676", "names": ["lung secondary", "lung metastasis", "LUNG METASTASIS", "lung metastases", "metastasis lung", "Lung metastases", "Lung Metastases", "lungs metastasis", "Lung secondaries", "lung secondaries", "metastasis to lung", "Metastases to Lung", "Metastases to lung", "Metastasis in lung", "Metastasis to Lung", "Metastasis to lung", "pulmonary secondary", "Pulmonary metastasis", "Pulmonary metastases", "Pulmonary Metastasis", "PULMONARY METASTASIS", "pulmonary metastases", "pulmonary metastasis", "secondary lung cancer", "secondary cancer lung", "cancer lung secondary", "LUNG CANCER METASTATIC", "Lung cancer metastatic", "cancer lung metastatic", "lung cancer metastatic", "metastatic cancer lung", "metastatic lung cancer", "Metastasis to the Lung", "Metastases to lung, NOS", "cancer lungs metastatic", "Secondary cancer of lung", "Cancer metastatic to lung", "metastatic cancer to lung", "cancer metastatic to lung", "cancer, metastatic to lung", "lung, metastatic cancer to", "Metastatic Tumor to the Lung", "Secondary malignancy of lung", "Metastatic Neoplasm to the Lung", "cancer with pulmonary metastases", "Secondary malignant tumor of lung", "Secondary malignant tumour of lung", "secondary malignant neoplasm of lung", "Secondary malignant neoplasm of lung", "Metastatic malignant neoplasm of lung", "Metastatic malignant neoplasm to lung", "metastasis of malignant neoplasm to lung", "Metastatic Malignant Neoplasm to the Lung", "Metastatic Malignant Neoplasm in the Lung", "Secondary malignant neoplasm of lung, NOS", "Metastatic malignant neoplasm to lung, NOS", "secondary malignant neoplasm of lung (diagnosis)", "Metastatic malignant neoplasm to lung (disorder)", "metastasis of malignant neoplasm to lung (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary malignant neoplasm of lung", "shortest_name_length": 14}
{"curie": "UMLS:C1262006", "names": ["bacterial sinusitis", "Bacterial sinusitis", "Sinusitis;bacterial", "sinusitis bacterial", "Sinusitis bacterial", "Bacterial sinusitis (disorder)", "bacterial sinusitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bacterial sinusitis", "shortest_name_length": 19}
{"curie": "UMLS:C1096001", "names": ["Application site swelling"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Application site swelling", "shortest_name_length": 25}
{"curie": "MONDO:0011585", "names": ["MNDJ", "HMNJ", "DSMA2", "dHMN2", "dHMNJ", "dSMA2", "distal spinal muscular atrophy 2", "spinal muscular atrophy Jerash type", "SPINAL MUSCULAR ATROPHY, JERASH TYPE", "Spinal muscular atrophy, Jerash type", "spinal muscular atrophy, Jerash type", "Distal spinal muscular atrophy type 2", "motor neuropathy, distal, Jerash type", "Motor neuropathy, distal, Jerash type", "Hereditary motor neuropathy, Jerash type", "hereditary motor neuropathy, Jerash type", "Distal hereditary motor neuropathy type 2", "Distal hereditary motor neuropathy Jerash type", "distal hereditary motor neuropathy Jerash type", "Distal hereditary motor neuropathy, Jerash type", "distal hereditary motor neuropathy, Jerash type", "Neuropathy, distal hereditary motor, Jerash type", "neuropathy, distal hereditary motor, Jerash type", "NEUROPATHY, DISTAL HEREDITARY MOTOR, JERASH TYPE", "Neuronopathy, Distal Hereditary Motor, Jerash Type", "NEURONOPATHY, DISTAL HEREDITARY MOTOR, JERASH TYPE", "neuronopathy, distal hereditary motor, Jerash type", "autosomal recessive distal spinal muscular atrophy 2", "spinal muscular atrophy, distal, autosomal recessive, 2", "SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 2", "Spinal Muscular Atrophy, Distal, Autosomal Recessive, 2", "autosomal recessive distal spinal muscular atrophy type 2", "Distal hereditary motor neuropathy Jerash type (disorder)", "Autosomal recessive distal spinal muscular atrophy type 2", "distal hereditary motor neuropathy, Jerash type (diagnosis)", "spinal muscular atrophy, distal, autosomal recessive, type 2", "spinal muscular atrophy distal hereditary motor neuropathy, Jerash type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive distal spinal muscular atrophy 2", "shortest_name_length": 4}
{"curie": "UMLS:C5239045", "names": ["Very High Risk Prostate Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Very High Risk Prostate Carcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C3831078", "names": ["Clinical Chorioamnionitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Chorioamnionitis", "shortest_name_length": 25}
{"curie": "MONDO:0024278", "names": ["Rectocolitis", "Colorectitis", "rectocolitis", "Proctocolitis", "proctocolitis", "Coloproctitis", "Colorectitis, NOS", "Coloproctitis, NOS", "Proctocolitis, NOS", "colorectum inflammation", "Proctocolitis (disorder)", "Proctocolitis (diagnosis)", "inflammation of colorectum", "colonic and rectal disorders proctocolitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "proctocolitis", "shortest_name_length": 12}
{"curie": "MONDO:0023149", "names": ["perfringens; Clostridium", "C. perfringens infection", "Clostridium; perfringens", "Clostridium perfringens Infection", "Clostridium perfringens infection", "Clostridium perfringens Infections", "Infection, Clostridium perfringens", "Infections, Clostridium perfringens", "Clostridioides perfringens Infection", "Clostridioides perfringens Infections", "Infection due to Clostridium perfringens", "infection due to clostridium perfringens", "Infection caused by Clostridium perfringens", "Clostridium perfringens infection (diagnosis)", "Infection due to Clostridium perfringens, NOS", "Infection caused by Clostridium perfringens (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infection due to clostridium perfringens", "shortest_name_length": 24}
{"curie": "MONDO:0032788", "names": ["CASVDD", "CEREBELLAR ATROPHY WITH SEIZURES AND VARIABLE DEVELOPMENTAL DELAY", "cerebellar atrophy with seizures and variable developmental delay"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellar atrophy with seizures and variable developmental delay", "shortest_name_length": 6}
{"curie": "UMLS:C2828031", "names": ["Stage IIA Skin Melanoma", "Stage IIA Skin Melanoma AJCC v6", "Stage IIA Skin Melanoma AJCC v7", "Stage IIA Cutaneous (Skin) Melanoma", "Stage IIA Cutaneous Melanoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Cutaneous Melanoma AJCC v6 and v7", "shortest_name_length": 23}
{"curie": "MONDO:0007110", "names": ["DBA", "BDS", "DBA1", "Aase syndrome", "AASE SYNDROME", "Aase-Smith syndrome 2", "AASE-SMITH SYNDROME II", "ERYTHROGENESIS IMPERFECTA", "BLACKFAN-DIAMOND SYNDROME", "Diamond-Blackfan Anemia 1", "Diamond-Blackfan anemia 1", "erythrogenesis imperfecta", "DIAMOND-BLACKFAN ANEMIA 1", "Blackfan-Diamond syndrome", "RPS19 Diamond-Blackfan anemia", "Diamond-Blackfan Anemia type 1", "RED CELL APLASIA, PURE, HEREDITARY", "Red cell aplasia, Pure, hereditary", "RPS19-related Diamond-Blackfan anemia", "AREGENERATIVE ANEMIA, CHRONIC CONGENITAL", "ANEMIA, CONGENITAL ERYTHROID HYPOPLASTIC", "aregenerative Anemia, chronic congenital", "anemia, congenital erythroid hypoplastic", "Diamond-Blackfan anemia caused by mutation in RPS19", "ANEMIA, CONGENITAL HYPOPLASTIC, OF BLACKFAN AND DIAMOND", "anemia, congenital hypoplastic, of Blackfan and Diamond"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diamond-Blackfan anemia 1", "shortest_name_length": 3}
{"curie": "UMLS:C0855071", "names": ["Localized Synovial Sarcoma", "Synovial Sarcoma Nonmetastatic", "Non-Metastatic Synovial Sarcoma", "Synovial sarcoma non-metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Synovial sarcoma non-metastatic", "shortest_name_length": 26}
{"curie": "UMLS:C0877096", "names": ["Application site paresthesia", "Application site paraesthesia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Application site paresthesia", "shortest_name_length": 28}
{"curie": "MONDO:0009986", "names": ["MIRHOSSEINI-HOLMES-WALTON SYNDROME", "Mirhosseini-Holmes-Walton syndrome", "retinopathy-mental retardation syndrome", "retinopathy pigmentary mental retardation", "Retinopathy pigmentary mental retardation", "[OBSOLETE] Mirhosseini-Holmes-Walton syndrome", "retinopathy pigmentary intellectual disability", "retinopathy, pigmentary, and mental retardation", "RETINOPATHY, PIGMENTARY, AND MENTAL RETARDATION", "Retinopathy, Pigmentary, And Mental Retardation", "pigmentary retinopathy-mental retardation syndrome", "retinopathy, pigmentary, and intellectual disability", "mental retardation-retinopathy-microcephaly syndrome", "microcephaly-mental retardation-retinopathy syndrome", "RETINOPATHY, PIGMENTARY, AND IMPAIRED INTELLECTUAL DEVELOPMENT", "retinal pigmentary degeneration-microcephaly-mental retardation syndrome", "retinal pigmentary degeneration, microcephaly, and severe mental retardation", "retinal pigmentary degeneration, microcephaly, and severe intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinopathy, pigmentary, and intellectual disability", "shortest_name_length": 34}
{"curie": "UMLS:C0278578", "names": ["stage IV cervix cancer", "cervix cancer, stage IV", "Stage IV Cervical Cancer", "Cervical Cancer Stage IV", "stage IV cervical cancer", "cervical cancer, stage IV", "Cervical Carcinoma Stage IV", "stage IV cancer of the cervix", "AJCC Stage IV Cervical Cancer", "FIGO Stage IV Cervix Carcinoma", "stage IV uterine cervix cancer", "cancer of the cervix, stage IV", "uterine cervix cancer, stage IV", "Stage IV Cervical Cancer AJCC v7", "stage IV carcinoma of the cervix", "Stage IV Cervical Cancer AJCC v6", "FIGO Stage IV Cervical Carcinoma", "FIGO Stage IV Carcinoma of Cervix", "carcinoma of the cervix, stage IV", "FIGO Stage IV Cervix Uteri Carcinoma", "FIGO Stage IV Carcinoma of the Cervix", "FIGO Stage IV Uterine Cervix Carcinoma", "FIGO Stage IV Carcinoma of Cervix Uteri", "Stage IV Cervical Cancer AJCC v6 and v7", "FIGO Stage IV Carcinoma of Uterine Cervix", "FIGO Stage IV Carcinoma of the Cervix Uteri", "FIGO Stage IV Carcinoma of the Uterine Cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Cervical Cancer AJCC v6 and v7", "shortest_name_length": 22}
{"curie": "MONDO:0018464", "names": ["severe PRPS1 superactivity", "severe PRPP synthetase superactivity", "severe phosphoribosylpyrophosphate synthetase superactivity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe phosphoribosylpyrophosphate synthetase superactivity", "shortest_name_length": 26}
{"curie": "MONDO:0000976", "names": ["paratesticular lipoma", "Paratesticular Lipoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paratesticular lipoma", "shortest_name_length": 21}
{"curie": "MONDO:0002568", "names": ["Narrow trachea", "Trachea narrowed", "trachea stenosis", "stenosis trachea", "Tracheal Stenosis", "trachea; stenosis", "tracheal stenosis", "TRACHEA, STENOSIS", "Tracheal Stenoses", "stenosis tracheal", "Trachea--Stenosis", "stenosis; trachea", "TRACHEAL STENOSIS", "Tracheal stenosis", "Stenoses, Tracheal", "Tracheal stricture", "stricture; trachea", "trachea; stricture", "Stenosis, Tracheal", "stenosis of trachea", "Stenosis of trachea", "Narrowing of windpipe", "Focal tracheal stenosis", "tracheal stenosis (diagnosis)", "Stenosis of trachea (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tracheal stenosis", "shortest_name_length": 14}
{"curie": "MONDO:0016536", "names": ["CD27 deficiency", "autosomal recessive lymphoproliferative disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive lymphoproliferative disease", "shortest_name_length": 15}
{"curie": "UMLS:C0302590", "names": ["calcium disorder", "CALCIUM DISORDER", "Calcium Disorders", "calcium disorders", "Disorder calcium (NOS)", "DISORDER CALCIUM (NOS)", "CALCIUM DISORDER (NOS)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disorder calcium (NOS)", "shortest_name_length": 16}
{"curie": "UMLS:C5667178", "names": ["Refractory HIV-Related Lymphoproliferative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory HIV-Related Lymphoproliferative Disorder", "shortest_name_length": 51}
{"curie": "MONDO:0011811", "names": ["SCAR4", "SCA24", "SCASI", "SCA24, FORMERLY", "spinocerebellar ataxia 24", "SPINOCEREBELLAR ATAXIA 24, FORMERLY", "spinocerebellar ataxia 24, formerly", "spinocerebellar ataxia 24 (formerly)", "autosomal recessive spinocerebellar ataxia 4", "spinocerebellar ataxia autosomal recessive 4", "spinocerebellar ataxia, autosomal recessive 4", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 4", "Spinocerebellar ataxia, autosomal recessive 4", "spinocerebellar ataxia with saccadic Intrusions", "Spinocerebellar ataxia with saccadic intrusions", "spinocerebellar ataxia with saccadic intrusions", "SPINOCEREBELLAR ATAXIA WITH SACCADIC INTRUSIONS", "Autosomal recessive cerebellar ataxia-movement disorder syndrome", "autosomal recessive cerebellar ataxia-saccadic intrusion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive cerebellar ataxia-saccadic intrusion syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0403379", "names": ["Emphysematous pyelonephritis", "emphysematous pyelonephritis", "pyelonephritis emphysematous", "Emphysematous pyelonephritis (disorder)", "Emphysematous pyelonephritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Emphysematous pyelonephritis", "shortest_name_length": 28}
{"curie": "MONDO:0019814", "names": ["straddling or overriding tricuspid valve"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "straddling or overriding tricuspid valve", "shortest_name_length": 40}
{"curie": "MONDO:0012565", "names": ["FANCN", "PALB2 Fanconi anemia", "Fanconi anemia complementation group N", "Fanconi Anemia, Complementation Group N", "Fanconi anemia, complementation group N", "FANCONI ANEMIA, COMPLEMENTATION GROUP N", "Fanconi anemia caused by mutation in PALB2", "Fanconi anemia complementation group type N", "Fanconi Anemia, complementation group type N", "Fanconi anemia complementation group N (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fanconi anemia complementation group N", "shortest_name_length": 5}
{"curie": "UMLS:C3897731", "names": ["Recurrent Primary Peritoneal Cancer", "Recurrent Primary Peritoneal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Primary Peritoneal Carcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C3641116", "names": ["In Utero Drug Withdrawal", "In-utero Drug Withdrawal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "In Utero Drug Withdrawal", "shortest_name_length": 24}
{"curie": "MONDO:0008683", "names": ["WT3", "Wilms Tumor 3", "Wilms tumor 3", "WILMS TUMOR 3", "Wilms tumor, type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wilms tumor 3", "shortest_name_length": 3}
{"curie": "UMLS:C0578159", "names": ["antibiotic-associated diarrhea", "Antibiotic-associated diarrhea", "Antibiotic associated diarrhea", "Antibiotic-Associated Diarrhea", "antibiotic associated diarrhea", "Antibiotic-associated diarrhoea", "Antibiotic associated diarrhoea", "antibiotics associated diarrhea", "Antibiotic-associated diarrhea (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Antibiotic-associated diarrhea", "shortest_name_length": 30}
{"curie": "MONDO:0007333", "names": ["VWS1", "Vdws", "lip-pit syndrome", "VAN DER WOUDE SYNDROME 1", "VAN DER Woude syndrome 1", "van der Woude syndrome 1", "IRF6 van der Woude syndrome", "Van Der Woude syndrome type 1", "van der Woude syndrome caused by mutation in IRF6", "cleft lip and/or palate with mucous cysts of Lower lip"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "van der Woude syndrome 1", "shortest_name_length": 4}
{"curie": "MONDO:0005019", "names": ["Diffuse Sclerosis", "Scleroderma;diffuse", "Diffuse Scleroderma", "diffuse scleroderma", "Diffuse scleroderma", "SCLERODERMA, DIFFUSE", "Scleroderma, Diffuse", "Progressive Scleroderma", "progressive scleroderma", "Sudden Onset Scleroderma", "Scleroderma, Progressive", "Scleroderma, Sudden Onset", "Sudden Onset Sclerodermas", "Diffuse Systemic Sclerosis", "diffuse systemic sclerosis", "Diffuse systemic sclerosis", "diffuse sclerosis systemic", "Diffuse Systemic Scleroses", "Sclerodermas, Sudden Onset", "Systemic sclerosis, diffuse", "Systemic Sclerosis, Diffuse", "systemic sclerosis, diffuse", "Scleroses, Diffuse Systemic", "Sclerosis, Diffuse Systemic", "Systemic Scleroses, Diffuse", "Diffuse cutaneous scleroderma", "Progressive Systemic Sclerosis", "Progressive systemic sclerosis", "progressive systemic sclerosis", "Systemic Sclerosis, Progressive", "Sclerosis, Progressive Systemic", "Diffuse Cutaneous Systemic Sclerosis", "PSS - Progressive systemic sclerosis", "Diffuse cutaneous systemic sclerosis", "Diffuse cutaneous systemic scleroderma", "Systemic sclerosis, diffuse (disorder)", "Progressive cutaneous systemic sclerosis", "Progressive systemic sclerosis (disorder)", "Progressive cutaneous systemic scleroderma", "progressive systemic sclerosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diffuse scleroderma", "shortest_name_length": 17}
{"curie": "MONDO:0007742", "names": ["HTOR", "5-hydroxytryptamine oxygenase regulator", "5-HYDROXYTRYPTAMINE OXYGENASE REGULATOR", "5-HYDROXYTRYPTAMINE oxygenase regulator"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "5-hydroxytryptamine oxygenase regulator", "shortest_name_length": 4}
{"curie": "MONDO:0008182", "names": ["NPLCS", "palpebral coloboma lipoma syndrome", "PALPEBRAL COLOBOMA-LIPOMA SYNDROME", "Palpebral coloboma lipoma Syndrome", "palpebral coloboma-lipoma syndrome", "Palpebral Coloboma-Lipoma Syndrome", "NASOPALPEBRAL LIPOMA-COLOBOMA SYNDROME", "Nasopalpebral lipoma coloboma syndrome", "Nasopalpebral lipoma-coloboma syndrome", "NASOPALPEBRAL lipoma-coloboma syndrome", "nasopalpebral lipoma-coloboma syndrome", "Nasopalpebral Lipoma-Coloboma Syndrome", "Nasopalpebral lipoma coloboma syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasopalpebral lipoma-coloboma syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0020701", "names": ["BDA1", "BRACHYDACTYLY, type A1", "brachydactyly type A1A", "Farabee-type Brachydactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly type A1A", "shortest_name_length": 4}
{"curie": "UMLS:C0589616", "names": ["Genitourinary chlamydia infection", "Genitourinary chlamydia infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Genitourinary chlamydia infection", "shortest_name_length": 33}
{"curie": "MONDO:0012711", "names": ["PPAB", "Beta-PPA", "BETA-PPA", "peripapillary atrophy, BETA type", "peripapillary atrophy, beta type", "PERIPAPILLARY ATROPHY, BETA TYPE", "Peripapillary Atrophy, Beta Type", "PERIPAPILLARY CHORIORETINAL ATROPHY, BETA TYPE", "peripapillary chorioretinal atrophy, Beta type", "Peripapillary Chorioretinal Atrophy, Beta Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peripapillary atrophy, beta type", "shortest_name_length": 4}
{"curie": "MONDO:0017134", "names": ["odonto onycho dysplasia with alopecia", "odonto-onycho dysplasia-alopecia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "odonto-onycho dysplasia-alopecia syndrome", "shortest_name_length": 37}
{"curie": "UMLS:C2363919", "names": ["Childhood depression", "Childhood Depression"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood depression", "shortest_name_length": 20}
{"curie": "MONDO:0005346", "names": ["Gallstones", "gallstones"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gallstones", "shortest_name_length": 10}
{"curie": "MONDO:0012816", "names": ["ATFB6", "atrial fibrillation familial 6", "atrial fibrillation, familial, 6", "ATRIAL FIBRILLATION, FAMILIAL, 6", "Atrial Fibrillation, Familial, 6", "NPPA familial atrial fibrillation", "atrial fibrillation, familial, type 6", "atrial fibrillation familial 6 (diagnosis)", "familial atrial fibrillation caused by mutation in NPPA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial fibrillation, familial, 6", "shortest_name_length": 5}
{"curie": "MONDO:0030886", "names": ["HPE14", "HOLOPROSENCEPHALY 14", "holoprosencephaly 14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "holoprosencephaly 14", "shortest_name_length": 5}
{"curie": "UMLS:C3272792", "names": ["Rectal SSA", "Rectal SSP", "Rectal SSA/P", "Rectal Sessile Serrated Polyp", "Rectal Sessile Serrated Adenoma", "Rectal Serrated Lesions and Polyps", "Rectal Sessile Serrated Adenoma/Polyp"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rectal Serrated Lesions and Polyps", "shortest_name_length": 10}
{"curie": "MONDO:0015634", "names": ["isolated osteopoikilosis", "isolated osteopoikilosis (disease)", "nonsyndromic osteopoikilosis (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated osteopoikilosis", "shortest_name_length": 24}
{"curie": "MONDO:0054654", "names": ["COXPD32", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 32", "combined oxidative phosphorylation deficiency 32"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation deficiency 32", "shortest_name_length": 7}
{"curie": "UMLS:C1710481", "names": ["Trichoepithelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Trichoepithelial Carcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0005170", "names": ["myeloid tumor", "Myeloid Tumor", "myeloid neoplasm", "Myeloid neoplasm", "Myeloid Neoplasm", "Myeloid neoplasia", "Myeloid malignancy", "myeloid malignancy", "Myeloid Malignancy", "Myeloid neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myeloid neoplasm", "shortest_name_length": 13}
{"curie": "MONDO:0021454", "names": ["Limbal dermoid", "benign eye tumor", "Benign Eye Tumor", "Benign eye tumor", "Epibulbar dermoid", "Benign eye tumour", "Epibulbar dermoids", "Benign Tumor of Eye", "Benign Ocular Tumor", "benign eye neoplasm", "benign tumor of eye", "Neoplasm benign;eye", "Benign Eye Neoplasm", "benign ocular tumor", "Benign tumor of eye", "eye benign neoplasm", "Benign tumour of eye", "Benign neoplasm of eye", "Benign Neoplasm of Eye", "benign ocular neoplasm", "benign neoplasm of eye", "Benign Ocular Neoplasm", "Benign eye neoplasm NOS", "benign tumor of the eye", "Benign Tumor of the Eye", "Ocular neoplasms benign", "Benign neoplasm of eyeball", "benign neoplasm of the eye", "Benign Neoplasm of the Eye", "Benign neoplasm of eye, NOS", "Benign neoplasm of eye (disorder)", "benign neoplasm of eye (diagnosis)", "Benign neoplasm of eye, unspecified", "Benign neoplasm of eye, part unspecified", "Benign neoplasm of unspecified part of eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of eye", "shortest_name_length": 14}
{"curie": "UMLS:C0423712", "names": ["Iliohypogastric neuralgia", "Iliohypogastric nerve neuralgia", "Iliohypogastric Nerve Neuralgia", "Iliohypogastric Nerve Neuralgias", "Nerve Neuralgia, Iliohypogastric", "Neuralgia, Iliohypogastric Nerve", "Nerve Neuralgias, Iliohypogastric", "Neuralgias, Iliohypogastric Nerve", "Iliohypogastric nerve neuralgia (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neuralgia, Iliohypogastric Nerve", "shortest_name_length": 25}
{"curie": "MONDO:0012943", "names": ["RP46", "retinitis pigmentosa 46", "RETINITIS PIGMENTOSA 46", "Retinitis Pigmentosa 46", "IDH3B retinitis pigmentosa", "retinitis pigmentosa type 46", "retinitis pigmentosa caused by mutation in IDH3B", "Retinitis Pigmentosa, Autosomal Recessive, Idh3b-Related", "retinitis pigmentosa, autosomal recessive, Idh3B-related", "RETINITIS PIGMENTOSA, AUTOSOMAL RECESSIVE, IDH3B-RELATED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 46", "shortest_name_length": 4}
{"curie": "MONDO:0023038", "names": ["eccentrochondrodysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eccentrochondrodysplasia", "shortest_name_length": 24}
{"curie": "UMLS:C4526979", "names": ["Stage IIIA Small Intestinal, Esophageal, Colorectal, Mesenteric, and Peritoneal GIST AJCC v8", "Stage IIIA Small Intestinal, Esophageal, Colorectal, Mesenteric, and Peritoneal Gastrointestinal Stromal Tumor (GIST)", "Stage IIIA Small Intestinal, Esophageal, Colorectal, Mesenteric, and Peritoneal Gastrointestinal Stromal Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Small Intestinal, Esophageal, Colorectal, Mesenteric, and Peritoneal Gastrointestinal Stromal Tumor AJCC v8", "shortest_name_length": 92}
{"curie": "UMLS:C4049242", "names": ["Acute lymphocytic leukemia refractory", "Acute lymphocytic leukaemia refractory"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute lymphocytic leukemia refractory", "shortest_name_length": 37}
{"curie": "MONDO:0005813", "names": ["Reticulum cell sarcoma", "dendritic cell sarcoma", "interdigitating cell sarcoma", "Interdigitating cell sarcoma", "Interdigitating Cell Sarcoma", "Interdigitating Cell Sarcomas", "Sarcoma, Interdigitating Cell", "Sarcomas, Interdigitating Cell", "interdigitating cell sarcoma/tumor", "Interdigitating Cell Sarcoma/Tumor", "interdigitating dendritic cell sarcoma", "Interdigitating Dendritic Cell Sarcoma", "Interdigitating dendritic cell sarcoma", "interdigitating Dendritic cell sarcoma", "Dendritic Cell Sarcoma, Interdigitating", "Interdigitating Dendritic Cell Sarcoma/Tumor", "interdigitating Dendritic cell sarcoma/tumor", "Interdigitating dendritic cell sarcoma (disorder)", "interdigitating dendritic cell sarcoma (diagnosis)", "Interdigitating dendritic cell sarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "interdigitating dendritic cell sarcoma", "shortest_name_length": 22}
{"curie": "UMLS:C4054127", "names": ["Radiation Nephropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radiation Nephropathy", "shortest_name_length": 21}
{"curie": "UMLS:C5557352", "names": ["Borderline Vulvar Phyllodes Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Vulvar Phyllodes Tumor", "shortest_name_length": 33}
{"curie": "MONDO:0021348", "names": ["tumor testis", "testis tumor", "testis tumors", "Tumor of testis", "testis neoplasm", "Testis Neoplasm", "tumor of testis", "Tumor of Testis", "Neoplasm, Testis", "Testicular tumor", "Testicular Tumor", "Tumour of testis", "tumor testicular", "Testis Neoplasms", "testicular tumor", "testicular tumour", "Tumor, Testicular", "Testicular tumour", "testicular tumors", "Testicular Tumors", "Neoplasms, Testis", "Testicular cancer", "Neoplasm of Testis", "Neoplasm of testis", "Tumors, Testicular", "neoplasm of testis", "testicular tumours", "Testicular neoplasm", "Testicular Neoplasm", "testicular neoplasm", "Tumor of the Testis", "tumor of the testis", "Neoplasm, Testicular", "neoplasms testicular", "Testicular Neoplasms", "Testicular neoplasia", "testicular neoplasms", "Neoplasms, Testicular", "Neoplasm of the Testis", "neoplasm of the testis", "Testicular neoplasm NOS", "testis neoplasm (disease)", "Neoplasm of testis (disorder)", "neoplasm of testis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplasm of testis", "shortest_name_length": 12}
{"curie": "UMLS:C4683424", "names": ["II 55 Years and Older", "Stage I Thyroid Gland Papillary Cancer 55 Years and Older", "Stage I Thyroid Gland Papillary Carcinoma 55 Years and Older AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Thyroid Gland Papillary Carcinoma 55 Years and Older AJCC v8", "shortest_name_length": 21}
{"curie": "MONDO:0002064", "names": ["breast angiomatosis", "Breast Angiomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast angiomatosis", "shortest_name_length": 19}
{"curie": "MONDO:0010951", "names": ["FDC", "CMD1B", "CMPD1", "dilated cardiomyopathy 1B", "cardiomyopathy, dilated 1B", "CARDIOMYOPATHY, DILATED, 1B", "cardiomyopathy, dilated, 1b", "cardiomyopathy, dilated, 1B", "dilated cardiomyopathy type 1B", "cardiomyopathy, familial dilated", "CARDIOMYOPATHY, FAMILIAL DILATED", "CARDIOMYOPATHY, FAMILIAL DILATED, 1", "cardiomyopathy, familial dilated, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1B", "shortest_name_length": 3}
{"curie": "UMLS:C0855175", "names": ["Bladder adenocarcinoma stage 0", "Stage 0 Bladder Adenocarcinoma", "Stage 0 Bladder Adenocarcinoma AJCC v6", "Stage 0 Bladder Adenocarcinoma AJCC v7", "Stage 0 Bladder Adenocarcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder adenocarcinoma stage 0", "shortest_name_length": 30}
{"curie": "MONDO:0017801", "names": ["atypical Meigs syndrome", "incomplete Meigs syndrome", "atypical Demons-Meigs syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical Meigs syndrome", "shortest_name_length": 23}
{"curie": "UMLS:C5419812", "names": ["Liver Neuroendocrine Tumor G2", "Hepatic Neuroendocrine Tumor G2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liver Neuroendocrine Tumor G2", "shortest_name_length": 29}
{"curie": "MONDO:0036483", "names": ["SRTD18", "short-rib thoracic dysplasia 18 with polydactyly", "SHORT-RIB THORACIC DYSPLASIA 18 WITH POLYDACTYLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short-rib thoracic dysplasia 18 with polydactyly", "shortest_name_length": 6}
{"curie": "MONDO:0003061", "names": ["Myoma", "myoma", "Myomas", "myomas", "muscle neoplasm", "Myomatous tumor", "myomatous tumor", "neoplasm of muscle", "Myomatous neoplasm", "Benign Muscle Tumor", "benign muscle tumor", "muscle tissue neoplasm", "benign tumor of muscle", "Benign tumor of muscle", "Benign muscle neoplasm", "muscle benign neoplasm", "Benign Tumor of Muscle", "Benign Muscle Neoplasm", "benign muscle neoplasm", "Benign tumour of muscle", "Benign Neoplasm of Muscle", "benign neoplasm of muscle", "Benign neoplasm of muscle", "Neoplasm benign;muscle(s)", "Benign Tumor of the Muscle", "Benign muscle neoplasm NOS", "benign tumor of the muscle", "benign neoplasm of the muscle", "Benign Neoplasm of the Muscle", "benign neoplasm of the Muscle", "Benign neoplasm of muscle, NOS", "Myoma (morphologic abnormality)", "benign neoplasm of the muscle(s)", "Benign neoplasm of muscle (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign muscle neoplasm", "shortest_name_length": 5}
{"curie": "MONDO:0012548", "names": ["SCN3", "Kostmann disease", "Kostmann syndrome", "agranulocytosis infantile", "infantile agranulocytosis", "agranulocytosis, infantile", "severe congenital neutropenia 3", "severe congenital neutropenia type 3", "severe congenital neutropenia autosomal recessive 3", "neutropenia, severe congenital 3, autosomal recessive", "neutropenia, severe congenital, 3, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kostmann syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0010441", "names": ["CKS", "CK syndrome", "CK SYNDROME", "CK syndrome (disorder)", "CK syndrome (diagnosis)", "CK syndrome, X-linked recessive", "mental retardation, X-linked, with thin body habitus and cortical malformation", "MENTAL RETARDATION, X-LINKED, WITH THIN BODY HABITUS AND CORTICAL MALFORMATION", "intellectual disability, X-linked, with thin body habitus and cortical malformation", "X-linked intellectual disability-microcephaly-cortical malformation-thin habitus syndrome", "X-linked intellectual disability, microcephaly, cortical malformation, thin habitus syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CK syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0003350", "names": ["Granular Cell Leiomyosarcoma", "granular cell leiomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "granular cell leiomyosarcoma", "shortest_name_length": 28}
{"curie": "UMLS:C1335120", "names": ["Mouth Lipoma", "Lipoma of Mouth", "Oral Cavity Lipoma", "Lipoma of the Mouth", "Lipoma of Oral Cavity", "Lipoma of the Oral Cavity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral Cavity Lipoma", "shortest_name_length": 12}
{"curie": "MONDO:0011555", "names": ["CTRUS", "RUSAT", "ATRUS syndrome", "THROMBOCYTOPENIA, CONGENITAL, WITH RADIOULNAR SYNOSTOSIS", "Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia", "radioulnar synostosis with amegakaryocytic thrombocytopenia", "radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome", "Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome", "Radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome", "Radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C4721664", "names": ["Esophagus Adenocarcinoma in situ", "Stage 0 Esophagus Adenocarcinoma", "Stage 0 Esophageal Adenocarcinoma", "Esophageal Adenocarcinoma in situ", "Esophageal Adenocarcinoma, Stage 0", "Oesophageal Adenocarcinoma Stage 0", "Adenocarcinoma in situ of Esophagus", "Stage 0 Adenocarcinoma of Esophagus", "Stage 0 Adenocarcinoma of the Esophagus", "Adenocarcinoma in situ of the Esophagus", "Stage 0 Esophageal Adenocarcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Esophageal Adenocarcinoma AJCC v7", "shortest_name_length": 32}
{"curie": "MONDO:0800106", "names": ["disruptive disorder", "disruptive behavior disorder", "Disruptive Behavior Disorder", "Disruptive behavior disorder", "behavior disorder disruptive", "DISRUPTIVE BEHAVIOR DISORDERS", "Behavior Disorder, Disruptive", "Disruptive behaviour disorder", "disruptive behavior disorders", "Disruptive Behavior Disorders", "Disruptive Behavioral Disorder", "behaviour disorders disruptive", "Disruptive Behavioral Disorders", "Behavioral Disorder, Disruptive", "Disorder, Disruptive Behavioral", "Disruptive behavior disorder NOS", "Disruptive behavior disorder, NOS", "Disruptive behavior disorder (disorder)", "disruptive behavior disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disruptive behavior disorder", "shortest_name_length": 19}
{"curie": "UMLS:C0852925", "names": ["Gastrointestinal necrosis", "Gastrointestinal tract necrosis", "Necrosis of gastrointestinal tract", "Necrosis of gastrointestinal tract (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Necrosis of gastrointestinal tract", "shortest_name_length": 25}
{"curie": "UMLS:C0347950", "names": ["asthma attack", "Asthma attack", "asthma attacks", "asthmatic attack", "Asthmatic attack", "asthma attack (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Asthma attack", "shortest_name_length": 13}
{"curie": "UMLS:C4727403", "names": ["Recurrent Thyroid Gland Medullary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Thyroid Gland Medullary Carcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0030489", "names": ["EBS2A", "epidermolysis bullosa simplex 2A, generalized severe", "EPIDERMOLYSIS BULLOSA SIMPLEX 2A, DOWLING-MEARA TYPE", "EPIDERMOLYSIS BULLOSA SIMPLEX 2A, GENERALIZED SEVERE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolysis bullosa simplex 2A, generalized severe", "shortest_name_length": 5}
{"curie": "MONDO:0005071", "names": ["Nerve Diseases", "disorder; nervous", "nervous; disorder", "NERVOUS DISORDERS", "neurologic disease", "NEUROLOGIC DISORDER", "neurologic disorder", "Neurologic Disorder", "Neurologic Diseases", "Neurologic Disorders", "Disease;neurological", "neurological disease", "Neurological disease", "neurologic disorders", "Disorder, Neurologic", "neurological disorder", "Neurological disorder", "Neurological Disorder", "Disorders, Neurologic", "Neurological Disorders", "neurological disorders", "Nervous System Disease", "nervous system disease", "Disorder, Neurological", "Nervous system disease", "NERVOUS SYSTEM DISORDER", "nervous system diseases", "Disease, Nervous System", "DISORDER NERVOUS SYSTEM", "Disorders, Neurological", "Nervous system disorder", "NEUROLOGIC DISORDER NOS", "Nervous System Diseases", "Nervous System Disorder", "Neurologic disorder NOS", "Nervous system diseases", "nervous system disorder", "Disorder nervous system", "Nervous System Disorders", "nervous system; disorder", "nervous system disorders", "Disorder, Nervous System", "Nervous system--Diseases", "Diseases, Nervous System", "Nervous system disorders", "Disorders, Nervous System", "disorders nervous systems", "Neurological disorder NOS", "disease of nervous system", "Disorder of nervous system", "disorder of nervous system", "Disorder of Nervous System", "nervous system disorder NOS", "Nervous system disorder NOS", "Diseases of the nervous system", "diseases of the nervous system", "Disorder of nervous system NOS", "disorders of the nervous system", "neurologic disorders (diagnosis)", "nervous system disease or disorder", "Unspecified Nervous System Problem", "Nervous system disease or syndrome", "disease or disorder of nervous system", "Disorder of nervous system (disorder)", "disease (or disorder); nervous system", "CENTR & PERIPH NERVOUS SYSTEM DISORDERS", "Unspecified disorders of nervous system", "Diseases of the nervous system (G00-G99)", "disease (or disorder); neurological, disorder, nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nervous system disorder", "shortest_name_length": 14}
{"curie": "MONDO:0000740", "names": ["Large adenoids", "Adenoids large", "enlarged adenoids", "Hypertrophy;adenoid", "Adenoid Hypertrophy", "adenoid hypertrophy", "ADENOID HYPERTROPHY", "Adenoid hypertrophy", "enlargement; adenoid", "hypertrophy; adenoid", "adenoid; enlargement", "adenoids hypertrophy", "adenoid; hypertrophy", "hypertrophy adenoids", "adenoidal hypertrophy", "Adenoidal hypertrophy", "ADENOIDS, HYPERTROPHY", "Adenoidal enlargement", "adenoids hypertrophied", "hypertrophy of adenoids", "Hypertrophy of adenoids", "Enlargement of adenoids", "Large adenoids (finding)", "Hypertrophy of adenoids alone", "adenoid hypertrophy (diagnosis)", "Hypertrophy of adenoids (disorder)", "Increased size of nasopharyngeal adenoids", "hypertrophy of adenoids (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenoid hypertrophy", "shortest_name_length": 14}
{"curie": "UMLS:C5418789", "names": ["Advanced Rectal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Rectal Squamous Cell Carcinoma", "shortest_name_length": 39}
{"curie": "UMLS:C0270224", "names": ["neonatal tetany", "Neonatal tetany", "Neonatal Tetany", "tetany; neonatal", "Tetany, Neonatal", "neonatal; tetany", "Neonatal Tetanies", "Tetanies, Neonatal", "Neonatal tetany NOS", "neonatal tetany (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tetany, Neonatal", "shortest_name_length": 15}
{"curie": "UMLS:C4745036", "names": ["Locally Advanced Microsatellite Stable Colorectal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Microsatellite Stable Colorectal Carcinoma", "shortest_name_length": 59}
{"curie": "UMLS:C0221040", "names": ["Dialysis Dementia", "Dialysis dementia", "DEMENTIA, DIALYSIS", "DEMENTIA DIALYTICA", "Dialysis Encephalopathy", "Dialysis encephalopathy", "Dialysis dementia (disorder)", "Dialysis dementia (diagnosis)", "Dialysis encephalopathy syndrome", "Progressive Dialysis Encephalopathy", "metabolic encephalopathy dialysis dementia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dialysis dementia", "shortest_name_length": 17}
{"curie": "MONDO:0002174", "names": ["macular pucker", "Retina Wrinkle", "Macular Pucker", "Macular pucker", "Pucker, Macular", "Macular Puckers", "Macular puckering", "macular puckering", "Epiretinal membrane", "Preretinal fibrosis", "Premacular Fibrosis", "Epiretinal Membrane", "Preretinal Membrane", "preretinal fibrosis", "Premacular Fibroses", "Epimacular Membrane", "Epimacular membrane", "preretinal membrane", "Preretinal membrane", "epiretinal membrane", "Premacular fibrosis", "Fibrosis, Premacular", "Membrane, Epimacular", "Epiretinal Membranes", "Epimacular Membranes", "Membrane, Epiretinal", "epiretinal membranes", "Preretinal Membranes", "Membrane, Preretinal", "Epiretinal membranes", "Cellophane maculopathy", "cellophane maculopathy", "Cellophane Maculopathy", "Maculopathy, Cellophane", "Cellophane Maculopathies", "Macular retinal puckering", "macular retinal puckering", "ERM - Epiretinal membrane", "Macular puckering of retina", "macular puckering of retina", "Surface Wrinkling Retinopathy", "macular puckering (diagnosis)", "Surface-Wrinkling Retinopathy", "Epiretinal membrane (disorder)", "macular puckering was observed", "Retinopathy, Surface-Wrinkling", "Surface-Wrinkling Retinopathies", "Epiretinal Membrane Macular Pucker", "Internal Limiting Membrane Disease", "macular puckering (physical finding)", "Epiretinal membrane (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "preretinal fibrosis", "shortest_name_length": 14}
{"curie": "MONDO:0013497", "names": ["OKT4D", "T4 epitope deficiency", "T4 EPITOPE DEFICIENCY", "Okt4 epitope deficiency", "OKT4 EPITOPE DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Okt4 epitope deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C0280426", "names": ["Adult T-cell lymphoma/leukemia stage IV", "Stage IV Adult T-Cell Leukemia/Lymphoma", "stage IV adult T-cell leukemia/lymphoma", "Stage IV Adult T-Cell Lymphoma/Leukemia", "Adult T-Cell Lymphoma/Leukemia Stage IV", "Adult T-cell lymphoma/leukaemia stage IV", "adult T-cell leukemia/lymphoma, stage IV", "metastatic adult T-cell leukemia/lymphoma", "adult T-cell leukemia/lymphoma, metastatic", "Ann Arbor Stage IV Adult T-Cell Leukemia/Lymphoma", "stage IV HTLV-I associated adult T-cell leukemia/lymphoma", "HTLV-1 Associated Adult T-Cell Lymphoma/Leukemia Stage IV", "Stage IV HTLV-1 Associated Adult T-Cell Lymphoma/Leukemia", "HTLV-I associated adult T-cell leukemia/lymphoma, stage IV", "metastatic HTLV-I associated adult T-cell leukemia/lymphoma", "Metastatic HTLV-1 Associated Adult T-Cell Lymphoma/Leukemia", "HTLV-I associated adult T-cell leukemia/lymphoma, metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult T-cell lymphoma/leukemia stage IV", "shortest_name_length": 39}
{"curie": "MONDO:0011426", "names": ["cerebellar ataxia", "ACERULOPLASMINEMIA", "Aceruloplasminemia", "aceruloplasminemia", "Aceruloplasminaemia", "hypoceruloplasminemia", "Hypoceruloplasminemia", "HYPOCERULOPLASMINEMIA", "Ceruloplasmin deficiency", "CERULOPLASMIN DEFICIENCY", "ceruloplasmin deficiency", "deficiency; ceruloplasmin", "ceruloplasmin; deficiency", "Deficiency of ferroxidase", "Deficiency of ceruloplasmin", "Deficiency of caeruloplasmin", "hypoceruloplasminemia, hereditary", "Hereditary ceruloplasmin deficiency", "hereditary ceruloplasmin deficiency", "Deficiency of ferroxidase (disorder)", "familial apoceruloplasmin deficiency", "systemic hemosiderosis due to aceruloplasminemia", "HEMOSIDEROSIS, SYSTEMIC, DUE TO ACERULOPLASMINEMIA", "Hemosiderosis, Systemic, due to Aceruloplasminemia", "hemosiderosis, systemic, due to aceruloplasminemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aceruloplasminemia", "shortest_name_length": 17}
{"curie": "UMLS:C3898833", "names": ["Hyperacute allograft rejection", "Hyperacute Allograft Rejection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyperacute allograft rejection", "shortest_name_length": 30}
{"curie": "UMLS:C1332908", "names": ["Cerebral Hodgkin Lymphoma", "Cerebral Hodgkin's Disease", "Cerebral Hodgkin's Lymphoma", "Primary Cerebral Hodgkin Lymphoma", "Primary Cerebral Hodgkin's Disease", "Primary Cerebral Hodgkin's Lymphoma", "Primary Hodgkin's Disease of Cerebrum", "Primary Hodgkin's Lymphoma of Cerebrum", "Primary Hodgkin's Disease of the Cerebrum", "Primary Hodgkin's Lymphoma of the Cerebrum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebral Hodgkin Lymphoma", "shortest_name_length": 25}
{"curie": "UMLS:C0272423", "names": ["Ear injury", "ear injury", "Ear Injury", "EAR INJURY", "Injury;ear", "ear; injury", "injury; ear", "ear injuries", "Injury of ear", "injury of ear", "injuries of ear", "Injury of ear NOS", "Injury of ear region", "Injury of ear (disorder)", "injury of ear (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of ear", "shortest_name_length": 10}
{"curie": "MONDO:0003430", "names": ["malignant Prolactinoma", "malignant prolactinoma", "Prolactin-producing pituitary tumor", "prolactin secreting pituitary tumor", "prolactin-producing pituitary tumor", "prolactin producing pituitary tumor", "pituitary tumor, prolactin producing", "Prolactin-producing pituitary tumour", "prolactin producing pituitary tumour", "Prolactin Secreting tumor of Pituitary", "prolactin secreting tumor of pituitary", "prolactin producing pituitary neoplasm", "prolactin secreting pituitary neoplasm", "prolactin producing tumor of pituitary", "PRL producing pituitary gland neoplasm", "Prolactin Secreting tumour of Pituitary", "prolactin-producing pituitary gland tumor", "prolactin secreting neoplasm of pituitary", "prolactin producing pituitary gland tumor", "prolactin secreting pituitary gland tumor", "prolactin producing neoplasm of pituitary", "prolactin producing tumor of the pituitary", "prolactin secreting tumor of the pituitary", "prolactin secreting pituitary gland neoplasm", "prolactin producing pituitary gland neoplasm", "prolactin-producing pituitary gland neoplasm", "Prolactin-Producing Pituitary Gland Neoplasm", "prolactin secreting tumor of pituitary gland", "prolactin producing tumor of pituitary gland", "prolactin secreting neoplasm of the pituitary", "prolactin producing neoplasm of the pituitary", "Prolactin-Producing Pituitary Gland Carcinoma", "prolactin producing neoplasm of pituitary gland", "prolactin secreting neoplasm of pituitary gland", "prolactin secreting tumor of the pituitary gland", "prolactin producing tumor of the pituitary gland", "prolactin secreting neoplasm of the pituitary gland", "prolactin producing neoplasm of the pituitary gland", "malignant prolactin producing neoplasm of pituitary gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prolactin producing pituitary tumor", "shortest_name_length": 22}
{"curie": "MONDO:0044303", "names": ["CHDED", "congenital heart defects and ectodermal dysplasia", "CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital heart defects and ectodermal dysplasia", "shortest_name_length": 5}
{"curie": "UMLS:C4049050", "names": ["Capdepont Teeth", "Teeth, Capdepont", "Opalescent dentin", "Opalescent Dentin", "Dentin, Opalescent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Opalescent dentin", "shortest_name_length": 15}
{"curie": "MONDO:0023297", "names": ["psoriasis guttate", "Guttate psoriasis", "Psoriasis guttata", "psoriasis guttata", "guttate psoriasis", "guttata; psoriasis", "psoriasis; guttata", "Guttate psoriasis (disorder)", "guttate psoriasis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "guttate psoriasis", "shortest_name_length": 17}
{"curie": "MONDO:0009399", "names": ["hyperphosphatemia, polyuria, and seizures", "HYPERPHOSPHATEMIA, POLYURIA, AND SEIZURES", "Hyperphosphatemia, Polyuria, and Seizures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperphosphatemia, polyuria, and seizures", "shortest_name_length": 41}
{"curie": "MONDO:0010359", "names": ["DENT2", "DENT DISEASE 2", "DENT disease 2", "Dent Disease 2", "OCRL Dent disease", "Dent disease type 2", "nephrolithiasis type 2", "Dent disease type 2 (disorder)", "dent disease 2, X-linked recessive", "Dent disease caused by mutation in OCRL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dent disease type 2", "shortest_name_length": 5}
{"curie": "UMLS:C0677696", "names": ["Stage II Burkitt Lymphoma", "contiguous stage II adult Burkitt lymphoma", "Stage II Contiguous Adult Burkitt Lymphoma", "Stage II Contiguous Adult Burkitt's Lymphoma", "Ann Arbor Stage II Contiguous Adult Burkitt Lymphoma", "Contiguous Adult Diffuse Small Non-Cleaved Cell Lymphoma Stage II", "Contiguous Stage II Adult Diffuse Small Non-Cleaved Cell Lymphoma", "contiguous stage II adult diffuse small noncleaved cell/Burkitt's lymphoma", "Contiguous Adult Diffuse Small Non-Cleaved Cell/Burkitt's Lymphoma Stage II", "Stage II Contiguous Adult Diffuse Small Non-Cleaved Cell/Burkitt's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage II Contiguous Adult Burkitt Lymphoma", "shortest_name_length": 25}
{"curie": "MONDO:0007391", "names": ["Coxa Vara", "COXA VARA", "coxa vara", "Coxa vara", "Coxa Varus", "vara; coxa", "Coxa Varas", "Vara, Coxa", "coxa; vara", "Varas, Coxa", "Varus, Coxa", "coxa vara (disease)", "Congenital Coxa Vara", "Coxa vara (disorder)", "Congenital coxa vara", "coxa vara (diagnosis)", "coxa vara, congenital", "Coxa Vara, Congenital", "Congenital Coxa Varas", "Congenital Coxa Varus", "Coxa vara, congenital", "coxa vara was observed", "Coxa Varas, Congenital", "Coxa Varus, Congenital", "Varus deformity of hip", "vara; coxa, congenital", "coxa; vara, congenital", "Hip joint - varus deformity", "coxa vara (physical finding)", "Congenital coxa vara (disorder)", "Varus deformity of hip (disorder)", "Hip joint varus deformity - observation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coxa vara", "shortest_name_length": 9}
{"curie": "MONDO:0018554", "names": ["PVOD and/or PCH", "pulmonary veno-occlusive disease and/or pulmonary capillary haemangiomatosis", "Pulmonary veno-occlusive disease and/or pulmonary capillary haemangiomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary veno-occlusive disease and/or pulmonary capillary haemangiomatosis", "shortest_name_length": 15}
{"curie": "UMLS:C0855043", "names": ["Localized Extraskeletal Ewing Sarcoma", "Non-Metastatic Extraosseous Ewing Sarcoma", "Non-Metastatic Extraskeletal Ewing Sarcoma", "Non-Metastatic Extraosseous Ewing's Sarcoma", "Extra-Osseous Ewing's Sarcoma, Nonmetastatic", "Non-Metastatic Extra-Osseous Ewing's Sarcoma", "Non-Metastatic Extraskeletal Ewing's Sarcoma", "Extra-osseous Ewing's sarcoma non-metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extra-osseous Ewing's sarcoma non-metastatic", "shortest_name_length": 37}
{"curie": "MONDO:0032932", "names": ["MTDPS18", "mitochondrial DNA depletion syndrome 18", "MITOCHONDRIAL DNA DEPLETION SYNDROME 18"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial DNA depletion syndrome 18", "shortest_name_length": 7}
{"curie": "MONDO:0041154", "names": ["disorder of neck of urinary bladder", "functional disorder of bladder neck and sphincter mechanism", "Functional disorder of bladder neck and sphincter mechanism", "Functional disorder of bladder neck and sphincter mechanism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of neck of urinary bladder", "shortest_name_length": 35}
{"curie": "UMLS:C5421325", "names": ["Indolent T-Cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Indolent T-Cell Non-Hodgkin Lymphoma", "shortest_name_length": 36}
{"curie": "MONDO:0018984", "names": ["Oroya fever", "Oroya Fever", "Oroya; fever", "Fever, Oroya", "fever; Oroya", "Carrión disease", "Carrion disease", "Carrión Disease", "Carrion Disease", "Disease, Carrion", "Cat scratch fever", "Carrion's Disease", "Carrion's disease", "Disease, Carrion's", "Oroya fever (disorder)", "Oroya fever (diagnosis)", "Bartonella bacilliformis Infection", "Bartonella bacilliformis Infections", "Infection, Bartonella bacilliformis", "Infection by Bartonella bacilliformis", "Bartonella bacilliformis infectious disease", "Infection caused by Bartonella bacilliformis", "Bartonella bacilliformis disease or disorder", "Bartonella bacilliformis caused disease or disorder", "Bartonellosis due to Bartonella bacilliformis infection", "bartonellosis due to Bartonella bacilliformis infection", "Infection caused by Bartonella bacilliformis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oroya fever", "shortest_name_length": 11}
{"curie": "UMLS:C0410198", "names": ["myopathy proximal", "Proximal myopathy", "MYOPATHY PROXIMAL", "proximal myopathy", "Myopathy, proximal", "Proximal myopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Proximal myopathy", "shortest_name_length": 17}
{"curie": "MONDO:0024331", "names": ["CRC", "Colorectal cancer", "colorectal cancer", "Colorectal Cancer", "COLORECTAL CANCER", "Large Bowel Cancer", "large bowel cancer", "Colorectal Cancers", "Colo-rectal cancer", "colorectal cancers", "colo-rectal cancer", "Cancer, Colorectal", "colon rectal cancer", "COLON RECTAL CANCER", "Cancers, Colorectal", "Colon/rectal cancer", "colorectal carcinoma", "Colorectal carcinoma", "Colorectal Carcinoma", "carcinoma colorectal", "colorectum carcinoma", "Carcinoma;bowel;large", "Carcinoma, Colorectal", "cancer of large bowel", "Colorectal carcinomas", "Large Bowel Carcinoma", "Colorectal cancer NOS", "Cancer of Large Bowel", "large bowel carcinoma", "Colorectal Carcinomas", "Colorectal cancer, NOS", "Large Intestine Cancer", "large intestine cancer", "Carcinomas, Colorectal", "carcinoma of colorectum", "carcinoma of large bowel", "Carcinoma of Large Bowel", "Cancer of Large Intestine", "Carcinoma;intestine;large", "Large intestine carcinoma", "cancer of large intestine", "Large Intestine Carcinoma", "large intestine carcinoma", "Cancer of the Large Bowel", "cancer of the large bowel", "carcinoma of large intestine", "Carcinoma of Large Intestine", "Carcinoma of the Large Bowel", "carcinoma of the large bowel", "colorectal cancer (diagnosis)", "Cancer of the Large Intestine", "cancer of the large intestine", "Carcinoma of the Large Intestine", "carcinoma of the large intestine", "colorectal (colon or rectal) cancer", "Colorectal (Colon or Rectal) Cancer", "carcinoma of large intestine (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorectal carcinoma", "shortest_name_length": 3}
{"curie": "UMLS:C0032964", "names": ["Hematologic Pregnancy Complication", "Hematologic Pregnancy Complications", "Pregnancy Complication, Hematologic", "Complication, Hematologic Pregnancy", "Hematological Pregnancy Complication", "Pregnancy, Hematologic Complications", "Pregnancy Complications, Hematologic", "Complications, Hematologic Pregnancy", "Complication, Hematological Pregnancy", "Hematological Pregnancy Complications", "Pregnancy Complication, Hematological", "Complications, Hematological Pregnancy", "Pregnancies, Hematologic Complications", "Pregnancy Complications, Hematological"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pregnancy Complications, Hematologic", "shortest_name_length": 34}
{"curie": "MONDO:0006458", "names": ["Thymoma Type B3", "type B3 thymoma", "thymoma type B3", "Squamoid Thymoma", "atypical thymoma", "Atypical Thymoma", "squamoid thymoma", "epithelial thymoma", "Epithelial Thymoma", "thymoma, epithelial", "Thymoma, epithelial", "Thymoma, type B3, NOS", "Thymoma, atypical, NOS", "Thymoma, epithelial, NOS", "Malignant Thymoma Type B3", "malignant thymoma type B3", "type B3 thymoma (diagnosis)", "Thymoma, type B3, malignant", "Epithelial Malignant Thymoma", "epithelial malignant thymoma", "Epithelial malignant thymoma", "Thymoma, atypical, malignant", "Thymoma, epithelial, malignant", "well-differentiated thymic carcinoma", "Well Differentiated Thymic Carcinoma", "well differentiated thymic carcinoma", "Well-Differentiated Thymic Carcinoma", "Well differentiated thymic carcinoma", "Thymoma, type B3, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thymoma type B3", "shortest_name_length": 15}
{"curie": "MONDO:0016845", "names": ["Del(21)(q22.11q22.12)", "monosomy 21q22.11q22.12", "monosomy 21q22.11-q22.12", "21q22.11q22.12 microdeletion syndrome", "21q22.11-q22.12 microdeletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "21q22.11q22.12 microdeletion syndrome", "shortest_name_length": 21}
{"curie": "MONDO:0010644", "names": ["low molecular weight proteinuria with hypercalciuric nephrocalcinosis", "Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis", "proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis", "PROTEINURIA, LOW MOLECULAR WEIGHT, WITH HYPERCALCIURIA AND NEPHROCALCINOSIS", "Proteinuria, Low Molecular Weight, with Hypercalciuria and Nephrocalcinosis", "proteinuria, low molecular weight, with hypercalciuric nephrocalcinosis, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis", "shortest_name_length": 69}
{"curie": "MONDO:0021487", "names": ["Benign Choroid Tumor", "benign choroid tumor", "Benign tumor of choroid", "benign choroid neoplasm", "Benign Choroid Neoplasm", "benign tumor of choroid", "Benign Tumor of Choroid", "Benign tumour of choroid", "Benign neoplasm of choroid", "benign neoplasm of choroid", "Benign Neoplasm of Choroid", "benign tumor of the choroid", "Benign Tumor of the Choroid", "optic choroid benign neoplasm", "Benign Neoplasm of the Choroid", "benign neoplasm of the choroid", "Benign neoplasm of choroid (disorder)", "benign neoplasm of choroid (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of choroid", "shortest_name_length": 20}
{"curie": "UMLS:C2981675", "names": ["Stage IB Pancreatic Cancer", "Stage IB Pancreatic Cancer AJCC v6 and v7", "Stage IB Exocrine and Endocrine Pancreatic Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Pancreatic Cancer AJCC v6 and v7", "shortest_name_length": 26}
{"curie": "UMLS:C5418905", "names": ["Advanced Carcinoma Of Unknown Primary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Carcinoma Of Unknown Primary", "shortest_name_length": 37}
{"curie": "UMLS:C0549124", "names": ["ARTERIAL EMBOLUS", "embolus arterial", "arterial embolus", "Arterial embolus", "Arterial Embolus", "arterial embolism", "Arterial embolism", "Embolism;arterial", "Embolism arterial", "EMBOLISM ARTERIAL", "embolism arterial", "Arterial Embolism", "embolism; arterial", "arterial embolisms", "Arterial embolism NOS", "Embolic arterial occlusion", "Arterial embolism (disorder)", "arterial embolism (diagnosis)", "Arterial embolism, NOS, of unspecified artery"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arterial embolism", "shortest_name_length": 16}
{"curie": "MONDO:0004958", "names": ["OCSC", "OSCC", "Mouth SCC", "mouth scc", "SCC of Mouth", "scc of mouth", "Oral Cavity SCC", "oral cavity scc", "SCC of the Mouth", "scc of the mouth", "scc of oral cavity", "SCC of Oral Cavity", "scc of the oral cavity", "SCC of the Oral Cavity", "Oral Squamous Cell Carcinoma", "oral squamous cell carcinoma", "Oral squamous cell carcinoma", "Mouth Squamous Cell Carcinoma", "squamous cell carcinoma mouth", "Oral Squamous Cell Carcinomas", "carcinoma cell mouth squamous", "mouth squamous cell carcinoma", "Oral Cavity Squamous Cell Cancer", "Squamous Cell Carcinoma of Mouth", "squamous cell carcinoma of mouth", "oral cavity squamous cell cancer", "Squamous cell carcinoma of mouth", "Oral Cavity Squamous Cell Carcinoma", "oral cavity squamous cell carcinoma", "squamous cell carcinoma of the mouth", "Squamous Cell Carcinoma of the Mouth", "Squamous Cell Carcinoma of Oral Cavity", "squamous cell carcinoma of oral cavity", "squamous cell carcinoma of the oral cavity", "Squamous cell carcinoma of the oral cavity", "Squamous Cell Carcinoma of the Oral Cavity", "Squamous cell carcinoma of mouth (disorder)", "malignant squamous cell neoplasm of oral cavity", "malignant squamous cell neoplasm of oral cavity (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oral cavity squamous cell carcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0007366", "names": ["BFNS2", "BFNC2", "EPILEPSY, BENIGN NEONATAL, 2", "Epilepsy, Benign Neonatal, 2", "seizures, benign neonatal, 2", "KCNQ3 benign neonatal seizures", "Benign familial neonatal seizures", "Seizures, Benign Familial Neonatal", "SEIZURES, BENIGN FAMILIAL NEONATAL, 2", "seizures, benign familial neonatal, 2", "convulsions, benign familial neonatal, 2", "CONVULSIONS, BENIGN FAMILIAL NEONATAL, 2", "Convulsions, Benign Familial Neonatal, 2", "seizures, benign familial neonatal, type 2", "Convulsions benign familial neonatal dominant form", "Autosomal dominant form of benign neonatal seizures", "benign neonatal seizures caused by mutation in KCNQ3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "seizures, benign familial neonatal, 2", "shortest_name_length": 5}
{"curie": "UMLS:C1336054", "names": ["Spindle Cell Type A Uveal Melanoma", "Uveal Spindle Cell Type A Melanoma", "Spindle Cell Type A Melanoma of Uvea", "type A spindle cell intraocular melanoma", "Spindle Cell Type A Melanoma of the Uvea", "spindle cell A type intraocular melanoma", "melanoma, spindle cell A type intraocular", "intraocular melanoma, spindle cell A type", "A type intraocular melanoma, spindle cell", "melanoma, intraocular, spindle cell A type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uveal Spindle Cell Type A Melanoma", "shortest_name_length": 34}
{"curie": "MONDO:0054736", "names": ["MVA3", "MOSAIC variegated aneuploidy syndrome 3", "mosaic variegated aneuploidy syndrome 3", "MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mosaic variegated aneuploidy syndrome 3", "shortest_name_length": 4}
{"curie": "MONDO:0019886", "names": ["Trisomy 13qter", "trisomy 13qter", "distal trisomy 13q", "Distal trisomy 13q", "Distal duplication 13q", "distal duplication 13q", "distal trisomy type 13q", "telomeric duplication 13q", "Telomeric duplication 13q", "Distal trisomy 13q (disorder)", "Distal trisomy 13q (diagnosis)", "anomaly of chromosome pair 13 partial trisomy 13q distal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal trisomy 13q", "shortest_name_length": 14}
{"curie": "MONDO:0000573", "names": ["recombinase activating gene 2 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "recombinase activating gene 2 deficiency", "shortest_name_length": 40}
{"curie": "UMLS:C4055466", "names": ["Soft Tissue Angiosarcoma", "Angiosarcoma of Soft Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Soft Tissue Angiosarcoma", "shortest_name_length": 24}
{"curie": "MONDO:0018713", "names": ["Hobnail Hemangioendothelioma", "hobnail hemangioendothelioma", "Retiform Hemangioendothelioma", "Retiform hemangioendothelioma", "retiform hemangioendothelioma", "Retiform haemangioendothelioma", "adult retiform hemangioendothelioma", "Retiform hemangioendothelioma (disorder)", "Retiform hemangioendothelioma (diagnosis)", "Retiform hemangioendothelioma (morphologic abnormality)", "neoplasm - soft tissue blood vessel hemangioendothelioma retiform"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retiform hemangioendothelioma", "shortest_name_length": 28}
{"curie": "MONDO:0030071", "names": ["RP89", "retinitis pigmentosa 89", "RETINITIS PIGMENTOSA 89"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 89", "shortest_name_length": 4}
{"curie": "MONDO:0013770", "names": ["ASD9", "ATRIAL SEPTAL DEFECT 9", "atrial septal defect 9", "atrial septal defect type 9", "atrial heart septal defect 9", "atrial septal defect 9 - ASD9", "GATA6 atrial heart septal defect", "atrial heart septal defect type 9", "atrial septal defect 9 - ASD9 (diagnosis)", "atrial heart septal defect caused by mutation in GATA6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial septal defect 9", "shortest_name_length": 4}
{"curie": "MONDO:0023201", "names": ["Fryns Smeets Thiry syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fryns Smeets Thiry syndrome", "shortest_name_length": 27}
{"curie": "MONDO:0018154", "names": ["Carpus curvus", "MADELUNG DEFORMITY", "Madelung deformity", "Madelung Deformity", "deformity; Madelung", "Madelung; deformity", "deformity madelung s", "madelung's deformity", "Madelung's deformity", "Madelung wrist deformity", "Madelung's deformity of wrist", "Madelung's deformity (disorder)", "Madelung's deformity (diagnosis)", "Madelung's deformity was observed", "Foreshortened ulna (Madelung deformity)", "Madelung's deformity of wrist (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Madelung deformity", "shortest_name_length": 13}
{"curie": "UMLS:C4744519", "names": ["Encapsulated Variant Thyroid Gland Papillary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Encapsulated Variant Thyroid Gland Papillary Carcinoma", "shortest_name_length": 54}
{"curie": "UMLS:C0456677", "names": ["Total spinal", "Total spinal block", "Total spinal blockade", "Total spinal blockade (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Total spinal blockade", "shortest_name_length": 12}
{"curie": "MONDO:0030724", "names": ["DFNA84", "DEAFNESS, AUTOSOMAL DOMINANT 84", "deafness, autosomal dominant 84", "hearing loss, autosomal dominant 84"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal dominant 84", "shortest_name_length": 6}
{"curie": "MONDO:0700138", "names": ["Bovine Rectal Myxoma", "bovine rectal myxoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bovine rectal myxoma", "shortest_name_length": 20}
{"curie": "MONDO:0011751", "names": ["COPD", "COPD, severe early onset", "COPD, severe early-onset", "pulmonary disease, chronic obstructive", "COPD, rate of decline of lung function in", "pulmonary disease, chronic obstructive, severe early-onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "COPD, severe early onset", "shortest_name_length": 4}
{"curie": "UMLS:C4744550", "names": ["Metastatic Nasopharyngeal Keratinizing Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Nasopharyngeal Keratinizing Squamous Cell Carcinoma", "shortest_name_length": 62}
{"curie": "UMLS:C5419868", "names": ["Low-Grade BilIN", "Low Grade BilIN", "Low Grade Biliary Intraepithelial Neoplasia", "Low-Grade Biliary Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Grade Biliary Intraepithelial Neoplasia", "shortest_name_length": 15}
{"curie": "UMLS:C1335916", "names": ["Sarcoma NCI Grade 1", "Sarcoma NCI Grade I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sarcoma NCI Grade 1", "shortest_name_length": 19}
{"curie": "MONDO:0018198", "names": ["AIEF", "AESD", "Acute infantile encephalopathy predominantly affecting frontal lobe", "Acute encephalopathy with biphasic seizures and late reduced diffusion", "acute encephalopathy with biphasic seizures and late reduced diffusion", "Acute infantile encephalopathy predominantly affecting the frontal lobes", "acute infantile encephalopathy predominantly affecting the frontal lobes", "Acute encephalopathy with biphasic seizures and late reduced diffusion (disorder)", "acute encephalopathy with biphasic seizures and late reduced diffusion (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute encephalopathy with biphasic seizures and late reduced diffusion", "shortest_name_length": 4}
{"curie": "MONDO:0008037", "names": ["myelinated optic nerve fibers", "MYELINATED OPTIC NERVE FIBERS", "myelinated optic nerve fibers (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myelinated optic nerve fibers", "shortest_name_length": 29}
{"curie": "UMLS:C2887088", "names": ["Sepsis due to Staphylococcus aureus", "Sepsis caused by Staphylococcus aureus", "Sepsis caused by Staphylococcus aureus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sepsis due to Staphylococcus aureus", "shortest_name_length": 35}
{"curie": "MONDO:0007153", "names": ["arteries, anomalies of", "ARTERIES, ANOMALIES OF", "ARTERIES, ANOMALIES OF (Radial)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arteries, anomalies of", "shortest_name_length": 22}
{"curie": "MONDO:0002995", "names": ["small intestinal NET", "Small Intestinal NET", "carcinoid tumor of small intestine", "small intestine neuroendocrine tumor", "Small Intestinal Neuroendocrine Tumor", "small intestinal neuroendocrine tumor", "Small Intestinal Well Differentiated Endocrine Tumor", "small intestinal well differentiated endocrine tumor", "Small Intestinal Well Differentiated Endocrine Tumor/Carcinoma", "small intestinal well differentiated endocrine tumor/carcinoma", "small intestine neuroendocrine tumor, well differentiated, low or intermediate grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small intestine neuroendocrine tumor, well differentiated, low or intermediate grade", "shortest_name_length": 20}
{"curie": "MONDO:0017406", "names": ["hypogonadotropic hypogonadism-severe microcephaly-sensorineural deafness-dysmorphism syndrome", "hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome", "shortest_name_length": 93}
{"curie": "MONDO:0021445", "names": ["Oral benign tumor", "Benign Oral Tumor", "benign mouth tumor", "benign oral tumors", "Benign Mouth Tumor", "Oral benign tumour", "Oral neoplasm benign", "Benign Oral Neoplasm", "ORAL NEOPLASM BENIGN", "benign mouth neoplasm", "Benign Tumor of Mouth", "Oral Neoplasm, Benign", "Benign Mouth Neoplasm", "benign tumor of mouth", "Benign neoplasm of mouth", "benign neoplasm of mouth", "Benign Neoplasm of Mouth", "Benign Oral Cavity Tumor", "benign oral cavity tumor", "benign tumor of the mouth", "Benign Tumor of the Mouth", "benign cavity oral tumors", "benign oral cavity neoplasm", "Benign tumor of oral cavity", "Benign Tumor of Oral Cavity", "benign tumor of oral cavity", "oral cavity benign neoplasm", "Benign Oral Cavity Neoplasm", "Benign tumour of oral cavity", "Benign oral cavity neoplasms", "Benign Neoplasm of the Mouth", "benign neoplasm of the mouth", "Benign neoplasm of mouth, NOS", "benign neoplasm of oral cavity", "Benign Neoplasm of Oral Cavity", "Benign neoplasm of oral cavity", "Benign Tumor of the Oral Cavity", "benign tumor of the oral cavity", "Benign Neoplasm of the Oral Cavity", "benign neoplasm of the oral cavity", "Benign neoplasm of the oral cavity NOS", "Benign neoplasm of oral cavity (disorder)", "benign neoplasm of oral cavity (diagnosis)", "benign neoplasm of oral cavity (non-specific)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of oral cavity", "shortest_name_length": 17}
{"curie": "MONDO:0006688", "names": ["brown lung", "Brown Lung", "Byssinoses", "byssinosis", "Mill fever", "BYSSINOSIS", "Byssinosis", "Brown Lungs", "stripper's asthma", "cotton mill fever", "Stripper's asthma", "Brown Lung Disease", "cotton dust asthma", "Cotton-dust asthma", "Strippers' disease", "Brown Lung Diseases", "Monday morning fever", "textile worker's lung", "Flax dressers disease", "Byssinosis (disorder)", "flax-dressers' disease", "Flax-dressers' disease", "Flax-dresser's disease", "flax-dresser's disease", "byssinosis (diagnosis)", "flax-dresser's; disease", "cotton dust pneumoconiosis", "Cotton workers' lung disease", "fibrosis; lung, with byssinosis", "lung; fibrosis, with byssinosis", "pneumoconiosis from cotton dust", "occupational asthma (byssinosis)", "Flax-dressers' disease (disorder)", "flax-dressers' disease (diagnosis)", "disease (or disorder); flax-dresser's", "disease (or disorder); respiratory tract, due to cotton dust"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "byssinosis", "shortest_name_length": 10}
{"curie": "MONDO:0007090", "names": ["AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM", "Amastia, Bilateral, With Ureteral Triplication And Dysmorphism", "amastia, bilateral, with ureteral triplication and dysmorphism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amastia, bilateral, with ureteral triplication and dysmorphism", "shortest_name_length": 62}
{"curie": "MONDO:0017093", "names": ["unilateral focal polymicrogyria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "unilateral focal polymicrogyria", "shortest_name_length": 31}
{"curie": "UMLS:C4683151", "names": ["Stage III Posterior Uveal Melanoma AJCC v8", "Stage III Choroidal and Ciliary Body Melanoma", "Stage III Choroidal and Ciliary Body Melanoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Choroidal and Ciliary Body Melanoma AJCC v8", "shortest_name_length": 42}
{"curie": "MONDO:0001615", "names": ["EKC", "Shipyard eye", "shipyard eye", "shipyard eye (diagnosis)", "Virus keratoconjunctivitis", "keratoconjunctivitis virus", "epidemic keratoconjunctivitis", "Epidemic Keratoconjunctivitis", "Epidemic keratoconjunctivitis", "KERATOCONJUNCTIVITIS, EPIDEMIC", "EKC - Epidemic keratoconjunctivitis", "Epidemic keratoconjunctivitis (disorder)", "epidemic keratoconjunctivitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidemic keratoconjunctivitis", "shortest_name_length": 3}
{"curie": "UMLS:C1708765", "names": ["Lung Adenocarcinoma, Mixed Subtype", "Mixed subtype adenocarcinoma of lung", "lung adenocarcinoma with mixed subtypes", "adenocarcinoma of lung with mixed subtypes", "Mixed subtype adenocarcinoma of lung (disorder)", "adenocarcinoma of lung with mixed subtypes (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mixed subtype adenocarcinoma of lung", "shortest_name_length": 34}
{"curie": "UMLS:C2983700", "names": ["Fallopian Tube Cancer by AJCC v6 Stage", "Fallopian Tube Carcinoma by AJCC v6 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fallopian Tube Cancer by AJCC v6 Stage", "shortest_name_length": 38}
{"curie": "UMLS:C0686463", "names": ["Metastasis to the Ciliary Body", "Metastatic Tumor to the Ciliary Body", "Metastatic Neoplasm to the Ciliary Body", "Secondary malignant neoplasm of ciliary body", "malignant neoplasm of ciliary body secondary", "Metastatic malignant neoplasm of ciliary body", "Metastatic malignant neoplasm to ciliary body", "Metastatic Malignant Neoplasm in the Ciliary Body", "Metastatic Malignant Neoplasm to the Ciliary Body", "Secondary malignant neoplasm of ciliary body (diagnosis)", "Metastatic malignant neoplasm to ciliary body (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to ciliary body", "shortest_name_length": 30}
{"curie": "UMLS:C0270786", "names": ["Binswanger", "Binswanger Disease", "binswanger disease", "Binswangers Disease", "binswangers disease", "Disease, Binswanger", "DEMENTIA BINSWANGER", "Binswanger's disease", "Binswanger's Disease", "binswanger's disease", "dementia binswanger's", "Disease, Binswanger's", "Binswanger's dementia", "binswanger's dementia", "binswanger encephalopathy", "Binswanger Encephalopathy", "Encephalopathy, Binswanger", "Binswanger's encephalopathy", "Binswanger's Encephalopathy", "binswanger's encephalopathy", "Encephalopathy, Binswangers", "Encephalopathy, Binswanger's", "Subcortical Leukoencephalopathy", "Subcortical leucoencephalopathy", "Subcortical leukoencephalopathy", "Leukoencephalopathy, Subcortical", "Subcortical Leukoencephalopathies", "Leukoencephalopathies, Subcortical", "Encephalitis subcorticalis chronica", "Subcortical atherosclerotic dementia", "DEMENTIA SUBCORTICAL ARTERIOSCLEROTIC", "Subcortical leukoencephalopathy (disorder)", "Subcortical arteriosclerotic encephalopathy", "Subcortical Arteriosclerotic Encephalopathy", "Encephalopathy, Subcortical Arteriosclerotic", "Arteriosclerotic Encephalopathy, Subcortical", "Subcortical Arteriosclerotic Encephalopathies", "Chronic Progressive Subcortical Encephalopathy", "Chronic progressive subcortical encephalopathy", "Arteriosclerotic Encephalopathies, Subcortical", "Encephalopathies, Subcortical Arteriosclerotic", "Subcortical Encephalopathy, Chronic Progressive", "Encephalopathy, Chronic Progressive Subcortical", "Encephalopathy, Subcortical, Chronic Progressive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Binswanger Disease", "shortest_name_length": 10}
{"curie": "UMLS:C4682803", "names": ["Stage II Testicular Cancer", "Stage II Testicular Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Testicular Cancer AJCC v8", "shortest_name_length": 26}
{"curie": "MONDO:0006021", "names": ["angina variant", "Variant angina", "angina inversa", "Variant Angina", "variant angina", "VARIANT ANGINA", "variant; angina", "PRINZMETAL ANGINA", "Prinzmetal Angina", "angina prinzmetal", "prinzmetal angina", "ANGINA PRINZMETAL", "Prinzmetal angina", "Vasospastic angina", "Prinzmetals Angina", "vasospastic angina", "Angina, Prinzmetal", "prinzmetals angina", "Prinzmetal; angina", "Prinzmetal's angina", "prinzmetal's angina", "Prinzmetal's Angina", "Angina, Prinzmetal's", "variant angina pectoris", "Variant angina pectoris", "Variant Angina Pectoris", "Angina Pectoris, Variant", "angina pectoris; variant", "PRINZMETAL VARIANT ANGINA", "prinzmetal variant angina", "ANGINA VARIANT PRINZMETAL", "Prinzmetal's variant angina", "ANGINA VARIANT <PRINZMETAL>", "Prinzmetal angina (disorder)", "Coronary artery spasm angina", "Prinzmetal's angina (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prinzmetal angina", "shortest_name_length": 14}
{"curie": "MONDO:0015367", "names": ["Charlie M syndrome", "Charlie M syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charlie M syndrome", "shortest_name_length": 18}
{"curie": "UMLS:C0278480", "names": ["Colon cancer Dukes C", "Dukes C colon cancer", "dukes c colon cancer", "colon cancer, Dukes C", "Colon cancer, stage 3", "stage III colon cancer", "stage iii colon cancer", "cancer colon iii stage", "Colon cancer stage III", "colon cancer stage iii", "Stage III Colon Cancer", "Carcinoma colon Dukes C", "colon cancer, stage III", "Dukes C Colon Carcinoma", "Colon carcinoma Dukes C", "Cancer of colon, stage 3", "Colonic cancer stage III", "Colon carcinoma stage III", "Dukes C Colonic Carcinoma", "Dukes C Carcinoma of Colon", "carcinoma of colon, stage III", "Carcinoma of colon, stage III", "Stage III Colon Cancer AJCC v6", "Colon Cancer Stage III AJCC v6", "AJCC Stage III Colon Cancer v6", "Dukes C Carcinoma of the Colon", "Colon Cancer, Stage III AJCC v6", "Stage III Colon Carcinoma AJCC v6", "Stage III Colonic Carcinoma AJCC v6", "Stage III Carcinoma of Colon AJCC v6", "Carcinoma of colon, stage III (finding)", "Stage III Carcinoma of the Colon AJCC v6", "carcinoma of colon, stage III (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Colon Cancer", "shortest_name_length": 20}
{"curie": "MONDO:0700021", "names": ["chromosome 14 disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 14 disorder", "shortest_name_length": 22}
{"curie": "MONDO:0011820", "names": ["IS2", "scoliosis, idiopathic 2", "SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 2", "scoliosis, isolated, susceptibility to, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scoliosis, isolated, susceptibility to, 2", "shortest_name_length": 3}
{"curie": "MONDO:0015823", "names": ["primary immunodeficiency due to a defect in adaptive immunity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary immunodeficiency due to a defect in adaptive immunity", "shortest_name_length": 61}
{"curie": "UMLS:C0036659", "names": ["sensation disorder", "Sensation Disorder", "sensation disorders", "sensation; disorder", "disorder; sensation", "Sensation Disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sensation Disorders", "shortest_name_length": 18}
{"curie": "MONDO:0012892", "names": ["BCARD", "LH3 Deficiency", "LH3 DEFICIENCY", "LH3 deficiency", "LYSYL HYDROXYLASE 3 DEFICIENCY", "Lysyl Hydroxylase 3 Deficiency", "lysyl Hydroxylase 3 deficiency", "Connective tissue disorder due to LH3 deficiency", "connective tissue disorder due to LH3 deficiency", "bone fragility-contractures-arterial rupture-deafness syndrome", "Bone fragility-contractures-arterial rupture-deafness syndrome", "bone fragility with contractures, arterial rupture, and deafness", "connective tissue disorder due to lysyl hydroxylase-3 deficiency", "BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS", "Bone Fragility with Contractures, Arterial Rupture, and Deafness", "Connective tissue disorder due to lysyl hydroxylase-3 deficiency", "Bone fragility, contractures, arterial rupture, deafness syndrome", "Bone fragillity, contractures, arterial rupture, deafness syndrome", "Bone fragility-contractures-arterial rupture-hearing loss syndrome", "disorders of connective tissue due to lysyl hydroxylase-3 deficiency", "Connective tissue disorder due to lysyl hydroxylase-3 deficiency (disorder)", "Connective tissue disorder due to lysyl hydroxylase-3 deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bone fragility with contractures, arterial rupture, and deafness", "shortest_name_length": 5}
{"curie": "MONDO:0001415", "names": ["Orchiatrophy", "atrophy testis", "testis atrophy", "atrophic testis", "testis; atrophy", "atrophy; testis", "TESTICLE ATROPHY", "testicle atrophy", "atrophy testicle", "Testis Atrophy of", "atrophy of testis", "Atrophy of testis", "atrophic testicle", "Atrophic testicle", "atrophy testicles", "testicular atrophy", "Testicular atrophy", "Testicular Atrophy", "Atrophy testicular", "TESTICULAR ATROPHY", "atrophied testicle", "ATROPHY TESTICULAR", "atrophy of testicle", "ATROPHY OF TESTICLE", "atrophied testicles", "Testicular degeneration", "Atrophy of testis (disorder)", "Atrophy of testis (diagnosis)", "testicular atrophy (physical finding)", "disorder of male genital organs atrophy of testis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrophy of testis", "shortest_name_length": 12}
{"curie": "UMLS:C1334322", "names": ["Keratinizing Primary Intraosseous Squamous Cell Carcinoma-Solid Type", "Keratinizing Primary Intraosseous Squamous Cell Carcinoma Arising de novo"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Keratinizing Primary Intraosseous Squamous Cell Carcinoma-Solid Type", "shortest_name_length": 68}
{"curie": "MONDO:0014285", "names": ["CDAN1B", "CDA, type IB", "CDA, type Ib", "CDA, TYPE Ib", "congenital dyserythropoietic anemia type Ib", "ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib", "anemia, congenital dyserythropoietic, type IB", "dyserythropoietic anemia, congenital, type IB", "congenital dyserythropoietic anemia type type 1B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital dyserythropoietic anemia type type 1B", "shortest_name_length": 6}
{"curie": "MONDO:0008262", "names": ["Poland", "Poland Anomaly", "Poland anomaly", "POLAND ANOMALY", "poland anomaly", "Poland sequence", "Poland anomalad", "Poland Sequence", "POLAND SEQUENCE", "poland syndrome", "Anomaly, Poland", "POLAND SYNDROME", "Poland syndrome", "Poland Syndrome", "anomaly polands", "poland's anomaly", "polands syndrome", "Syndrome Polands", "Poland's anomaly", "SYNDROME POLANDS", "Syndrome, Poland", "Poland's anomalad", "POLAND'S SYNDROME", "Poland's syndrome", "POLAND SYNDACTYLY", "poland's syndrome", "Poland syndactyly", "Poland Syndactyly", "Syndactyly, Poland", "Poland's syndactyly", "Poland anomaly (disorder)", "poland syndrome (diagnosis)", "pectoralis muscle, absence of", "Pectoralis Muscle, Absence of", "PECTORALIS MUSCLE, ABSENCE OF", "Unilateral defect of pectoralis muscle and syndactyly of hand", "Unilateral defect of pectoralis muscle AND syndactyly of hand", "unilateral defect of pectoralis muscle and syndactyly of the hand"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Poland syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0025690", "names": ["MEDS2", "MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME 2", "microcephaly, epilepsy, and diabetes syndrome 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly, epilepsy, and diabetes syndrome 2", "shortest_name_length": 5}
{"curie": "UMLS:C4683586", "names": ["Lugano Classification Stage I Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage I Hodgkin Lymphoma AJCC v8", "shortest_name_length": 54}
{"curie": "MONDO:0007769", "names": ["Dark eyelids", "dark eyelids", "Brown eyelids", "eyelid; chloasma", "chloasma; eyelid", "Chloasma of eyelid", "pigmentation; eyelids", "eyelids; pigmentation", "Blepharal pigmentation", "Pigmentation of eyelids", "EYELID HYPERPIGMENTATION", "dyspigmentation of eyelid", "Dyspigmentation of eyelid", "Hyperpigmentation of eyelid", "hyperpigmentation of eyelid", "Hyperpigmentation of Eyelids", "hyperpigmentation of eyelids", "HYPERPIGMENTATION OF EYELIDS", "Hyperpigmentation of eyelids", "Hyperpigmentation of eyelid, NOS", "Hyperpigmentation of eyelid (disorder)", "hyperpigmentation of eyelid (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperpigmentation of eyelid", "shortest_name_length": 12}
{"curie": "MONDO:0020555", "names": ["type I pleuropulmonary blastoma", "Pleuropulmonary blastoma type I", "pleuropulmonary blastoma type 1", "Type I Pleuropulmonary Blastoma", "Pleuro-pulmonary blastoma type I", "Pleuropulmonary blastoma type I (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pleuropulmonary blastoma type 1", "shortest_name_length": 31}
{"curie": "UMLS:C0424332", "names": ["breathhold", "breathholding", "Breathholding", "attack breath holding", "Breath holding attack", "Breath holding attacks", "breath holding attacks", "Breath holding with temper", "Breath holding with temper (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breath holding with temper", "shortest_name_length": 10}
{"curie": "UMLS:C4745189", "names": ["Adrenal Gland Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adrenal Gland Sarcoma", "shortest_name_length": 21}
{"curie": "UMLS:C0151694", "names": ["Hemorrhage colon", "HEMORRHAGE COLON", "hemorrhage; colon", "Haemorrhage colon", "Colon hemorrhagic", "colon; hemorrhage", "Colonic hemorrhage", "Colonic Hemorrhage", "HEMORRHAGE OF COLON", "Colonic haemorrhage", "Hemorrhage of colon", "Haemorrhage of colon", "Hemorrhage of colon (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemorrhage of colon", "shortest_name_length": 16}
{"curie": "MONDO:0013858", "names": ["PTCD", "PONTINE TEGMENTAL CAP DYSPLASIA", "pontine tegmental cap dysplasia", "PONTINE tegmental CAP dysplasia", "Pontine tegmental cap dysplasia", "PTCD - pontine tegmental cap dysplasia", "Pontine tegmental cap dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pontine tegmental cap dysplasia", "shortest_name_length": 4}
{"curie": "MONDO:0016646", "names": ["autosomal dominant optic atrophy and peripheral neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant optic atrophy and peripheral neuropathy", "shortest_name_length": 58}
{"curie": "MONDO:0030867", "names": ["THC7", "thrombocytopenia 7", "THROMBOCYTOPENIA 7", "Thrombocytopenia, Autosomal Dominant, 7", "THROMBOCYTOPENIA, AUTOSOMAL DOMINANT, 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombocytopenia 7", "shortest_name_length": 4}
{"curie": "MONDO:0019011", "names": ["CMT1", "HMSN1", "HMSN I", "HMSN Type I", "HSMN, type 1", "HSMN, type I", "HMN Distal Type I", "Charcot-Marie-Tooth type 1", "Charcot-Marie-Tooth disease type 1", "Charcot Marie Tooth Disease, Type I", "Charcot-Marie-Tooth disease, type I", "Charcot-Marie-Tooth Disease, Type I", "Charcot Marie Tooth disease, type 1", "Charcot-Marie-Tooth disease type T 1", "Charcot-Marie-Tooth neuropathy type 1", "HEREDITARY MOTOR AND SENSORY NEUROPATHY I", "Inherited dominant hypertrophic neuropathy", "Hereditary sensory-motor neuropathy, type I", "Hereditary sensory-motor neuropathy, type 1", "Hypertrophic neuropathy, inherited, dominant", "Hereditary Type I Motor and Sensory Neuropathy", "Hereditary motor and sensory neuropathy type 1", "Charcot-Marie-Tooth disease, type I (disorder)", "Hereditary Motor and Sensory Neuropathy Type I", "hereditary motor and sensory neuropathy type 1", "Hereditary motor and sensory neuropathy type I", "Neuropathy, Type I Hereditary Motor and Sensory", "Peroneal muscular atrophy of demyelinating type", "Hereditary Motor, and Sensory Neuropathy Type I", "Charcot-Marie-Tooth disease type T 1 (diagnosis)", "Charcot-Marie-Tooth disease of demyelinating type", "autosomal dominant demyelinating Charcot-Marie-Tooth disease", "Autosomal dominant demyelinating Charcot-Marie-Tooth disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 1", "shortest_name_length": 4}
{"curie": "MONDO:0023644", "names": ["Oral Cancer", "oral cancer", "oral carcinoma", "Oral Carcinoma", "Lip and oral cavity cancer", "oral cavity and lip cancer", "Lip and Oral Cavity Cancer", "lip and oral cavity cancer", "lip and oral cavity carcinoma", "Lip and Oral Cavity Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lip and oral cavity carcinoma", "shortest_name_length": 11}
{"curie": "UMLS:C2984093", "names": ["Gallbladder Cancer by AJCC v7 Stage", "Gallbladder Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gallbladder Cancer by AJCC v7 Stage", "shortest_name_length": 35}
{"curie": "UMLS:C4744547", "names": ["Metastatic Adrenal Cortex Carcinoma", "Metastatic Adrenal Cortical Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Adrenal Cortical Carcinoma", "shortest_name_length": 35}
{"curie": "MONDO:0007508", "names": ["RHS", "OFC8, included", "orofacial cleft 8", "RAPP-HODGKIN SYNDROME", "Rapp-Hodgkin syndrome", "Ectodermal Dysplasia Anhidrotic", "Anhidrotic Ectodermal Dysplasia", "Anhidrotic ectodermal dysplasia", "Anhydrotic Ectodermal Dysplasia", "Anhydrotic Ectodermal Dysplasias", "Ectodermal Dysplasia, Anhidrotic", "Dysplasia, Anhydrotic Ectodermal", "Ectodermal Dysplasia, Anhydrotic", "Ectodermal dysplasia, anhidrotic", "Anhidrotic, Ectodermal Dysplasia", "Dysplasia Anhidrotic, Ectodermal", "Dysplasia, Anhidrotic Ectodermal", "Anhidrotic Ectodermal Dysplasias", "Anhidrotics, Ectodermal Dysplasia", "Dysplasia Anhidrotics, Ectodermal", "Dysplasias, Anhidrotic Ectodermal", "Ectodermal Dysplasias, Anhydrotic", "Ectodermal dysplasia (anhidrotic)", "Ectodermal Dysplasias, Anhidrotic", "Dysplasias, Anhydrotic Ectodermal", "ectodermal dysplasia, Rapp-Hodgkin type", "Anhidrotic ectodermal dysplasia syndrome", "Rapp-Hodgkin type of ectodermal dysplasia", "Rapp-Hodgkin ectodermal dysplasia syndrome", "ectodermal dysplasia syndrome, Rapp-Hodgkin type", "anhidrotic ectodermal dysplasia with cleft lip/palate", "ectodermal dysplasia, anhidrotic, with cleft lip-palate", "cleft lip with or without cleft palate, nonsyndromic, 8", "ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP/PALATE", "ectodermal dysplasia, anhidrotic, with cleft Lip/palate", "Ectodermal dysplasia, anhidrotic, with cleft lip-palate", "autosomal dominant hypohidrotic ectodermal dysplasia syndrome", "Autosomal dominant hypohidrotic ectodermal dysplasia syndrome", "Hypohidrotic ectodermal dysplasia syndrome, autosomal dominant type", "Autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder)", "autosomal dominant hypohidrotic ectodermal dysplasia syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rapp-Hodgkin syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C0542052", "names": ["Insufficiency;coronary", "CORONARY INSUFFICIENCY", "Coronary insufficiency", "coronary insufficiency", "coronary; insufficiency", "insufficiency; coronary", "Coronary artery insufficiency", "INSUFFICIENCY CORONARY ARTERY", "Insufficiency coronary artery", "coronary artery insufficiency", "ARTERIAL INSUFFICIENCY CORONARY", "Arterial insufficiency coronary", "arterial insufficiency coronary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Coronary artery insufficiency", "shortest_name_length": 22}
{"curie": "MONDO:0000873", "names": ["LBL", "Lymphoblastoma", "lymphoblastoma", "Lymphoblastic lymphoma", "lymphoblastic lymphoma", "Diffuse lymphoblastoma", "LYMPHOMA LYMPHOBLASTIC", "lymphoma lymphoblastic", "Lymphoblastic Lymphoma", "lymphoma, lymphoblastic", "lymphoma; lymphoblastic", "Lymphoblastoma, diffuse", "lymphoblastic; lymphoma", "Lymphoblastic lymphoma NOS", "Lymphoblastic lymphosarcoma", "Diffuse lymphoblastic lymphoma", "Lymphoblastic lymphoma, diffuse", "Lymphoblastic malignant lymphoma", "precursor lymphoblastic lymphoma", "Malignant lymphoblastic lymphoma", "Precursor Lymphoblastic Lymphoma", "Lymphoblastic (diffuse) lymphoma", "Malignant lymphoma, lymphoblastic", "Lymphoblastic lymphoma (disorder)", "Malignant lymphoma - lymphoblastic", "lymphoma, lymphoblastic, malignant", "LYMPHOMA, LYMPHOBLASTIC, MALIGNANT", "diffuse lymphoblastic lymphoma (LL)", "Diffuse lymphoblastic lymphosarcoma", "Malignant lymphoma, convoluted cell", "Lymphoblastic lymphosarcoma, diffuse", "precursor cell lymphoblastic lymphoma", "Precursor cell lymphoblastic lymphoma", "Precursor Cell Lymphoblastic Lymphoma", "Diffuse lymphoblastic malignant lymphoma", "Lymphoblastic (diffuse) non-Hodgkin's lymphoma", "diffuse lymphoblastic lymphoma (LL) (diagnosis)", "Precursor cell lymphoblastic lymphoma (disorder)", "Precursor cell lymphoblastic lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphoblastic lymphoma", "shortest_name_length": 3}
{"curie": "MONDO:0021994", "names": ["Berk-Tabatznik syndrome", "Berk Tabatznik syndrome", "kyphosis brachyphalangy optic atrophy", "Kyphosis brachyphalangy optic atrophy", "congenital optic atrophy and brachytelephalangy", "Congenital optic atrophy and brachytelephalangy", "Cleft nare, brachydactyly, short stature-dwarfism", "cleft nare, brachydactyly, short stature-dwarfism", "cleft nare, brachydactyly, short stature dwarfism", "short stature, congenital optic atrophy, and hypoplasia of the cervical vertebral bodies and distal phalanges"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Berk-Tabatznik syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0019337", "names": ["Bullous disorder", "bullous disorder", "Bullous disorders", "bullous disorders", "bullous; disorder", "dermatoses bullous", "Bullous Dermatoses", "Dermatosis bullous", "bullous dermatitis", "dermatitis bullous", "Bullous dermatitis", "bullous dermatosis", "Dermatitis bullous", "dermatosis bullous", "bullous dermatoses", "Bullous dermatoses", "Bullous dermatosis", "Bullous Dermatitis", "Dermatoses, Bullous", "bullous; dermatosis", "dermatosis; bullous", "Bullous Skin Disease", "bullous skin disease", "bullous skin disorder", "Bullous Skin Diseases", "Skin Disease, Bullous", "Skin Diseases, Bullous", "Bullous dermatosis, NOS", "Bullous dermatitis, NOS", "Bullous disorders (L10-L14)", "bullous disorder (diagnosis)", "Bullous dermatosis (disorder)", "Bullous disorder, unspecified", "bullous dermatoses (diagnosis)", "disease (or disorder); bullous", "Unspecified bullous dermatoses", "autoimmune bullous skin disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune bullous skin disease", "shortest_name_length": 16}
{"curie": "UMLS:C1333627", "names": ["Follicular Hyperplasia of BALT", "Pulmonary Lymphoid Hyperplasia", "Follicular Bronchitis/Bronchiolitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Follicular Bronchitis/Bronchiolitis", "shortest_name_length": 30}
{"curie": "MONDO:0021441", "names": ["Benign Exocrine Pancreas Tumor", "benign exocrine pancreas tumor", "benign tumor of exocrine pancreas", "Benign Exocrine Pancreas Neoplasm", "benign exocrine pancreas neoplasm", "Benign tumor of exocrine pancreas", "Benign Tumor of Exocrine Pancreas", "exocrine pancreas benign neoplasm", "Benign tumour of exocrine pancreas", "benign exocrine pancreatic neoplasm", "Benign Exocrine Pancreatic Neoplasm", "benign neoplasm of exocrine pancreas", "Benign Neoplasm of Exocrine Pancreas", "Benign neoplasm of exocrine pancreas", "benign tumor of the exocrine pancreas", "Benign Tumor of the Exocrine Pancreas", "benign neoplasm of the exocrine pancreas", "Benign Neoplasm of the Exocrine Pancreas", "Benign tumor of exocrine pancreas (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of exocrine pancreas", "shortest_name_length": 30}
{"curie": "MONDO:0018246", "names": ["homozygous 2p21 microdeletion syndrome", "2p21 contiguous gene deletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "homozygous 2p21 microdeletion syndrome", "shortest_name_length": 38}
{"curie": "UMLS:C1335446", "names": ["Poorly Differentiated Prostate Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Poorly Differentiated Prostate Adenocarcinoma", "shortest_name_length": 45}
{"curie": "MONDO:0010164", "names": ["AARRS", "LPHAS", "Al Awadi syndrome", "Severe limb deficit", "severe limb deficit", "Phocomelia Schinzel type", "Schinzel type phocomelia", "Phocomelia, Schinzel type", "phocomelia, Schinzel type", "Schinzel phocomelia syndrome", "SCHINZEL PHOCOMELIA SYNDROME", "Al Awadi Teebi Farag syndrome", "Teebi Naguib Al Awadi syndrome", "Al-Awadi-Raas-Rothschild syndrome", "Al-Awadi-Raas-Rothschild Syndrome", "AL-AWADI/RAAS-ROTHSCHILD SYNDROME", "Al Awadi-Raas-Rothschild syndrome", "Al Awadi Rass Rothschild syndrome", "Al-Awadi/Raas-Rothschild syndrome", "Phocomelia Schinzel type (disorder)", "Congenital absence of ulna and fibula", "congenital absence of ulna and fibula", "aplasia/hypoplasia of limbs and pelvis", "Aplasia/hypoplasia of limbs and pelvis", "limb/pelvis-hypoplasia/aplasia syndrome", "Limb-Pelvis Hypoplasia-Aplasia syndrome", "Limb-Pelvis-Hypoplasia-Aplasia Syndrome", "LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME", "Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome", "Ulna and fibula absence of with severe limb deficiency", "absence of ulna and fibula with severe limb deficiency", "ulna and fibula absence of with severe limb deficiency", "ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY", "ulna and fibula, absence of, with severe limb deficiency", "Ulna And Fibula, Absence Of, With Severe Limb Deficiency", "profound limb deficiency, thoracic dystrophy, unusual facies, and normal intelligence"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phocomelia, Schinzel type", "shortest_name_length": 5}
{"curie": "MONDO:0010166", "names": ["ULNAR AGENESIS AND ENDOCARDIAL FIBROELASTOSIS", "ulnar agenesis and endocardial fibroelastosis", "Ulnar Agenesis and Endocardial Fibroelastosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ulnar agenesis and endocardial fibroelastosis", "shortest_name_length": 45}
{"curie": "UMLS:C0279803", "names": ["hypopharynx cancer, recurrent", "Relapsed Cancer of Hypopharynx", "Relapsed Hypopharyngeal Cancer", "Hypopharyngeal cancer recurrent", "recurrent hypopharyngeal cancer", "Recurrent Cancer of Hypopharynx", "hypopharyngeal cancer, recurrent", "Relapsed Cancer of the Hypopharynx", "Recurrent Cancer of the Hypopharynx", "Malignant neoplasm of hypopharynx recurrent", "Recurrent Malignant Hypopharyngeal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant neoplasm of hypopharynx recurrent", "shortest_name_length": 29}
{"curie": "UMLS:C4524752", "names": ["Recurrent Classic Hodgkin Lymphoma", "Relapsed Classical Hodgkin Lymphoma", "Recurrent Classical Hodgkin Lymphoma", "Relapsing classical Hodgkin lymphoma", "Classical Hodgkin lymphoma recurrent", "classical Hodgkin lymphoma, in relapse", "Relapsing classical Hodgkin lymphoma (disorder)", "classical Hodgkin lymphoma, in relapse (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Relapsing classical Hodgkin lymphoma", "shortest_name_length": 34}
{"curie": "MONDO:0014058", "names": ["fils", "FILS", "fils syndrome", "facial dysmorphism, immunodeficiency, livedo, and short stature", "FACIAL DYSMORPHISM, IMMUNODEFICIENCY, LIVEDO, AND SHORT STATURE", "facial dysmorphism-immunodeficiency-livedo-short stature syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "facial dysmorphism-immunodeficiency-livedo-short stature syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0007086", "names": ["ATS3", "Alport syndrome dominant type", "Alport syndrome autosomal dominant", "Autosomal dominant Alport syndrome", "autosomal dominant Alport syndrome", "Alport syndrome, autosomal dominant", "Alport Syndrome, Autosomal Dominant", "Alport syndrome 3, autosomal dominant", "ALPORT SYNDROME 3, AUTOSOMAL DOMINANT", "renal failure and sensorineural hearing loss", "Alport syndrome autosomal dominant (disorder)", "Alport syndrome autosomal dominant (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant Alport syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0014746", "names": ["CDG2N", "CDGIIn", "CDGIIdn", "CDG IIn", "CDG-IIn", "SLC39A8-CDG", "SLC39A8 deficiency", "CDG syndrome type IIn", "Congenital disorder of glycosylation type 2n", "congenital disorder of glycosylation type 2n", "SLC39A8 congenital disorder of glycosylation", "Congenital disorder of glycosylation type IIn", "congenital disorder of glycosylation type IIn", "congenital disorder of glycosylation, type IIn", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIn", "carbohydrate deficient glycoprotein syndrome type IIn", "Carbohydrate deficient glycoprotein syndrome type IIn", "Solute carrier family 39 member 8 congenital disorder of glycosylation", "Solute carrier family 39 member 8 congenital disorder of glycosylation (disorder)", "SLC39A8-CDG - solute carrier family 39 member 8 congenital disorder of glycosylation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SLC39A8-CDG", "shortest_name_length": 5}
{"curie": "MONDO:0700124", "names": ["chromosome 21 disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 21 disorder", "shortest_name_length": 22}
{"curie": "MONDO:0013536", "names": ["HMOX1D", "HO-1 deficiency", "Heme Oxygenase 1 Deficiency", "Heme oxygenase-1 deficiency", "HEME OXYGENASE 1 DEFICIENCY", "heme oxygenase-1 deficiency", "heme oxygenase 1 deficiency", "HO-1 (heme oxygenase-1) deficiency", "Heme oxygenase-1 deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heme oxygenase 1 deficiency", "shortest_name_length": 6}
{"curie": "MONDO:0002859", "names": ["breast rhabdomyosarcoma", "Breast Rhabdomyosarcoma", "rhabdomyosarcoma of breast", "Rhabdomyosarcoma of Breast", "Rhabdomyosarcoma of the Breast", "Rhabdomyosarcoma of the breast", "rhabdomyosarcoma of the breast", "breast rhabdomyosarcoma (disease)", "rhabdomyosarcoma (disease) of breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast rhabdomyosarcoma", "shortest_name_length": 23}
{"curie": "MONDO:0007415", "names": ["MC3DN1", "Isolated complex III deficiency", "Mitochondrial complex III deficiency", "Mitochondrial Complex III Deficiency", "mitochondrial complex III deficiency", "Deficiency of mitochondrial complex III", "BCS1L mitochondrial complex III deficiency", "Isolated CoQ-cytochrome C reductase deficiency", "Deficiency of isolated CoQ cytochrome c reductase", "Deficiency of mitochondrial complex III (disorder)", "mitochondrial Complex 3 deficiency, nuclear type 1", "mitochondrial complex III deficiency nuclear type 1", "Deficiency of ubiquinone cytochrome c oxidoreductase", "mitochondrial complex III deficiency, nuclear type 1", "MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1", "Complex 3 mitochondrial respiratory chain deficiency", "Isolated coenzyme Q-cytochrome C reductase deficiency", "Isolated ubiquinone-cytochrome C reductase deficiency", "Isolated mitochondrial respiratory chain complex III deficiency", "mitochondrial complex III deficiency caused by mutation in BCS1L"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex III deficiency nuclear type 1", "shortest_name_length": 6}
{"curie": "MONDO:0021573", "names": ["OOMD2", "OOCYTE MATURATION DEFECT 2", "oocyte maturation defect 2", "TUBB8 inherited oocyte maturation defect", "inherited oocyte maturation defect caused by mutation in TUBB8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oocyte maturation defect 2", "shortest_name_length": 5}
{"curie": "UMLS:C0205852", "names": ["Neoplasms, Embryonal and Mixed"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplasms, Embryonal and Mixed", "shortest_name_length": 30}
{"curie": "UMLS:C0010398", "names": ["Cruveilhier-Baumgarten", "Baumgarten-Cruveilhier", "Cruveilhier Baumgarten Disease", "Cruveilhier-Baumgarten Disease", "Disease, Cruveilhier-Baumgarten", "Cruveilhier Baumgarten Syndrome", "cruveilhier-baumgarten syndrome", "cruveilhier baumgarten syndrome", "Cruveilhier-Baumgarten Syndrome", "Cruveilhier-Baumgarten syndrome", "Syndrome, Cruveilhier-Baumgarten", "Cruveilhier-Baumgarten; cirrhosis", "Baumgarten-Cruveilhier; cirrhosis", "cirrhosis; Baumgarten-Cruveilhier", "cirrhosis; Cruveilhier-Baumgarten", "cirrhosis Cruveilhier-Baumgarten syndrome", "Cruveilhier-Baumgarten syndrome (disorder)", "Cruveilhier-Baumgarten syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cruveilhier-Baumgarten Syndrome", "shortest_name_length": 22}
{"curie": "MONDO:0045002", "names": ["vertebra disease", "vertebral disorder", "disease of vertebra", "Disorder of vertebra", "disorder of vertebra", "vertebra disease or disorder", "disease or disorder of vertebra", "Disorder of vertebra (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vertebral disorder", "shortest_name_length": 16}
{"curie": "MONDO:0008466", "names": ["KNS", "Karsch Neugebauer syndrome", "Karsch-Neugebauer syndrome", "KARSCH-NEUGEBAUER SYNDROME", "split hand nystagmus syndrome", "Split hand nystagmus syndrome", "NYSTAGMUS-SPLIT HAND SYNDROME", "Nystagmus-Split Hand Syndrome", "Nystagmus-split hand syndrome", "split hand split foot nystagmus", "Split hand split foot nystagmus", "Karsch Neugebauer syndrome (disorder)", "Split hand/split foot-nystagmus syndrome", "split hand/split foot-nystagmus syndrome", "split-hand with congenital NYSTAGMUS, fundal changes, and cataracts", "SPLIT-HAND WITH CONGENITAL NYSTAGMUS, FUNDAL CHANGES, AND CATARACTS", "Split-Hand With Congenital Nystagmus, Fundal Changes, And Cataracts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Karsch-Neugebauer syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C5421210", "names": ["Refractory Transformed Marginal Zone Lymphoma to Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Transformed Marginal Zone Lymphoma to Diffuse Large B-Cell Lymphoma", "shortest_name_length": 78}
{"curie": "MONDO:0014151", "names": ["PHN", "susceptibility to neonatal pulmonary hypertension", "PULMONARY HYPERTENSION, NEONATAL, SUSCEPTIBILITY TO", "pulmonary hypertension, neonatal, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary hypertension, neonatal, susceptibility to", "shortest_name_length": 3}
{"curie": "MONDO:0017319", "names": ["HE", "Ovalocytes", "Elliptocyte", "OVALOCYTOSIS", "ovalocytosis", "Ovalocytosis", "Elliptocytosis", "elliptocytosis", "Elliptocytosis NOS", "erythrocytosis; oval", "oval; erythrocytosis", "Hereditary Ovalocytosis", "Hereditary ovalocytosis", "Hereditary Ovalocytoses", "Congenital ovalocytosis", "hereditary ovalocytosis", "Elliptocytosis (finding)", "Ovalocytoses, Hereditary", "Hereditary eliptocytosis", "Ovalocytosis, Hereditary", "congenital elliptocytosis", "Hereditary Elliptocytosis", "Congenital elliptocytosis", "elliptocytosis hereditary", "Hereditary Elliptocytoses", "hereditary elliptocytosis", "Elliptocytosis hereditary", "Hereditary elliptocytosis", "Elliptocytoses, Hereditary", "ELLIPTOCYTOSIS, HEREDITARY", "Elliptocytosis, Hereditary", "Elliptocytosis (congenital)", "Congenital ovalocytosis, NOS", "Hereditary ovalocytosis, NOS", "Congenital elliptocytosis, NOS", "HE - Hereditary elliptocytosis", "Hereditary elliptocytosis, NOS", "hereditary hemolytic ovalocytosis", "hereditary ovalocytosis (diagnosis)", "hereditary hemolytic elliptocytosis", "Hereditary elliptocytosis (disorder)", "hereditary elliptocytosis (diagnosis)", "Ovalocytosis (congenital) (hereditary)", "disease (or disorder); hemoglobin or Hb, elliptocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary elliptocytosis", "shortest_name_length": 2}
{"curie": "UMLS:C0334479", "names": ["Angiomyosarcoma", "angiomyosarcoma", "angiomyosarcoma (diagnosis)", "Angiomyosarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Angiomyosarcoma", "shortest_name_length": 15}
{"curie": "MONDO:0021944", "names": ["ANSD", "Auditory neuropathy", "Auditory Neuropathy", "auditory neuropathy", "AUDITORY NEUROPATHY", "auditory dys-synchrony", "Auditory dys-synchrony", "Auditory Dys-synchrony", "Familial auditory neuropathy", "familial auditory neuropathy", "auditory neuropathy (diagnosis)", "progressive auditory neuropathy", "Progressive auditory neuropathy", "auditory neuropathy spectrum disorder", "Auditory Neuropathy Spectrum Disorder", "Auditory neuropathy spectrum disorder", "Auditory neuropathy with dys-synchrony", "Auditory neuropathy spectrum disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "auditory neuropathy", "shortest_name_length": 4}
{"curie": "UMLS:C0235964", "names": ["RENAL DYSGENESIS", "Renal dysgenesis", "dysgenesis; kidney", "kidney; dysgenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal dysgenesis", "shortest_name_length": 16}
{"curie": "UMLS:C0521586", "names": ["Gastrointestinal mucosal necrosis", "Gastrointestinal mucosal necrosis (disorder)", "Gastrointestinal mucosal necrosis (diagnosis)", "disorder of gastrointestinal tract mucosal necrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal mucosal necrosis", "shortest_name_length": 33}
{"curie": "MONDO:0017127", "names": ["genetic soft tissue tumor", "genetic mesenchymal tumor", "inherited soft tissue tumor", "genetic mesenchymal cell neoplasm", "hereditary mesenchymal cell neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited soft tissue tumor", "shortest_name_length": 25}
{"curie": "MONDO:0006622", "names": ["vulvar seborrheic keratosis", "Vulvar Seborrheic Keratosis", "Seborrheic Keratosis of Vulva", "seborrheic keratosis of vulva", "Seborrheic Keratosis of the Vulva", "seborrheic keratosis of the vulva", "mammalian vulva seborrheic keratosis", "seborrheic keratosis of mammalian vulva"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar seborrheic keratosis", "shortest_name_length": 27}
{"curie": "MONDO:0013454", "names": ["LCA11", "LEBER CONGENITAL AMAUROSIS 11", "Leber Congenital Amaurosis 11", "Leber congenital amaurosis 11", "IMPDH1 Leber congenital amaurosis", "Leber congenital amaurosis type 11", "amaurosis congenita of Leber, type 11", "Leber congenital amaurosis caused by mutation in IMPDH1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leber congenital amaurosis 11", "shortest_name_length": 5}
{"curie": "MONDO:0060768", "names": ["Fibrous epulis", "Fibromatous epulis", "Gum Fibroepithelial Polyp", "gum fibroepithelial polyp", "fibroepithelial polyp of gum", "Fibroepithelial Polyp of Gum", "Gingival Fibroepithelial Polyp", "Gingival fibroepithelial polyp", "gingival fibroepithelial polyp", "fibroepithelial polyp of gingiva", "fibroepithelial polyp of the gum", "Fibroepithelial Polyp of Gingiva", "Fibroepithelial Polyp of the Gum", "FEP - Gingival fibroepithelial polyp", "fibroepithelial polyp of the gingiva", "Fibroepithelial Polyp of the Gingiva", "FEP (fibroepithelial polyp) of gingiva", "Gingival fibroepithelial polyp (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gingival fibroepithelial polyp", "shortest_name_length": 14}
{"curie": "MONDO:0016039", "names": ["IDF", "Reye Tumor", "Reye tumor", "Reye tumour", "Reye's Tumor", "Reye's tumor", "Digital fibromatosis", "Infantile digital fibroma", "Inclusion Body Fibromatosis", "inclusion body fibromatosis", "Inclusion body fibromatosis", "Digital Fibrous Tumor of Reye", "Digital fibrous tumor of Reye", "digital fibrous tumor of Reye", "infantile digital fibromatosis", "Digital fibrous tumour of Reye", "Infantile Digital Fibromatosis", "Infantile digital fibromatosis", "Infantile digital myofibroblastoma", "inclusion body fibromatosis (disease)", "infantile digital fibroma/fibromatosis", "Recurrent digital fibroma of childhood", "Infantile Digital Fibroma/Fibromatosis", "Infantile digital fibromatosis (disorder)", "Recurring digital fibrous tumor of childhood", "recurring digital fibrous tumor of childhood", "asymptomatic nodular proliferation of fibrous tissue on the dorsal and lateral aspects of the fingers or toes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile digital fibromatosis", "shortest_name_length": 3}
{"curie": "MONDO:0004288", "names": ["Breast Scirrhous Carcinoma", "breast scirrhous carcinoma", "Scirrhous Breast Carcinoma", "scirrhous breast carcinoma", "scirrhous carcinoma of breast", "Scirrhous carcinoma of breast", "Scirrhous Carcinoma of Breast", "Duct carcinoma, desmoplastic type", "scirrhous carcinoma of the breast", "Scirrhous Carcinoma of the Breast", "breast malignant carcinoma scirrhous", "Scirrhous carcinoma of breast (disorder)", "scirrhous carcinoma of breast (diagnosis)", "infiltrating carcinoma of breast with fibrotic Stroma", "Infiltrating carcinoma of breast with Fibrotic Stroma", "Infiltrating Carcinoma of Breast with Fibrotic Stroma", "Infiltrating Carcinoma of the Breast with Fibrotic Stroma", "infiltrating carcinoma of the breast with fibrotic Stroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scirrhous breast carcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0002269", "names": ["cholera morbus", "GASTROENTERITIS", "Gastroenteritis", "gastroenteritis", "Gastroenteritides", "gastroenteritides", "Gastroenteritis NOS", "gastroenteritis nos", "GE - Gastroenteritis", "Gastroenteritis, NOS", "intestine inflammation", "inflammation of intestine", "gastroenteritis (diagnosis)", "Gastrointestinal tract inflamed", "Inflammation of stomach and intestine", "Inflammation of stomach and intestine (disorder)", "infectious colitis, enteritis and gastroenteritis", "Inflammation of the mucous membrane of the stomach and bowel"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastroenteritis", "shortest_name_length": 14}
{"curie": "MONDO:0030909", "names": ["MRXSHG", "syndromic X-linked mental retardation Hough type", "mental retardation, X-linked, syndromic, Houge type", "mental retardation, X-linked, syndromic, HOUGE type", "MENTAL RETARDATION, X-LINKED, SYNDROMIC, HOUGE TYPE", "syndromic X-linked intellectual disability Hough type", "intellectual disability, X-linked, syndromic, Houge type", "intellectual disability, X-linked, syndromic, HOUGE type", "intellectual developmental disorder, X-linked, syndromic, Houge type", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, HOUGE TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked, syndromic, Houge type", "shortest_name_length": 6}
{"curie": "MONDO:0009456", "names": ["Immunoerythromyeloid hypoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immunoerythromyeloid hypoplasia", "shortest_name_length": 31}
{"curie": "MONDO:0030258", "names": ["PCH14", "Pontocerebellar hypoplasia type 14", "pontocerebellar hypoplasia type 14", "PONTOCEREBELLAR HYPOPLASIA, TYPE 14", "pontocerebellar hypoplasia, type 14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pontocerebellar hypoplasia, type 14", "shortest_name_length": 5}
{"curie": "UMLS:C3899650", "names": ["Childhood Non-Small Cell Lung Cancer", "Childhood Lung Non-Small Cell Carcinoma", "Childhood Non-Small Cell Lung Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Lung Non-Small Cell Carcinoma", "shortest_name_length": 36}
{"curie": "MONDO:0007584", "names": ["exostoses-anetodermia-brachydactyly type E syndrome", "Exostoses with Anetodermia and Brachydactyly, Type E", "EXOSTOSES WITH ANETODERMIA AND BRACHYDACTYLY, TYPE E", "exostoses with anetodermia and brachydactyly, type E"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exostoses-anetodermia-brachydactyly type E syndrome", "shortest_name_length": 51}
{"curie": "UMLS:C4682561", "names": ["Stage IIIB Uterine Corpus Leiomyosarcoma", "Stage IIIB Uterine Corpus Leiomyosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Uterine Corpus Leiomyosarcoma AJCC v8", "shortest_name_length": 40}
{"curie": "UMLS:C1142077", "names": ["sinusitis fungal", "Fungal sinusitis", "fungal sinusitis", "Sinusitis fungal", "Fungal sinusitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fungal sinusitis", "shortest_name_length": 16}
{"curie": "MONDO:0003946", "names": ["vagina villous adenoma", "vaginal villous adenoma", "Vaginal Villous Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vaginal villous adenoma", "shortest_name_length": 22}
{"curie": "MONDO:0011167", "names": ["T1D6", "AITD5", "IDDM6", "type 1 diabetes mellitus 6", "TYPE 1 DIABETES MELLITUS 6", "Insulin-Dependent Diabetes Mellitus 6", "insulin-dependent diabetes mellitus 6", "INSULIN-DEPENDENT DIABETES MELLITUS 6", "Diabetes Mellitus, Insulin-Dependent, 6", "DIABETES MELLITUS, INSULIN-DEPENDENT, 6", "diabetes mellitus, insulin-dependent, 6", "autoimmune thyroid disease, susceptibility to, 5", "AUTOIMMUNE THYROID DISEASE, SUSCEPTIBILITY TO, 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type 1 diabetes mellitus 6", "shortest_name_length": 4}
{"curie": "UMLS:C1707545", "names": ["Skin Fibrous Histiocytoma, Fibroblastic Variant", "Cutaneous Fibrous Histiocytoma, Fibroblastic Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin Fibrous Histiocytoma, Fibroblastic Variant", "shortest_name_length": 47}
{"curie": "UMLS:C4054378", "names": ["Nephrotic Syndrome - LMX1B Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - LMX1B Associated", "shortest_name_length": 37}
{"curie": "MONDO:0010029", "names": ["Situs Inversus", "situs ambiguus", "inversus situs", "Situs Ambiguus", "situs inversus", "SITUS INVERSUS", "Situs inversus", "Inversus, Situs", "situs oppositus", "situs transversus", "Situs transversus", "Visceral inversion", "Laterality sequence", "laterality sequence", "Complete transposition", "transposition; viscera", "viscera; transposition", "situs inversus totalis", "Situs inversus totalis", "situs viscerum inversus", "Situs inversus viscerum", "Situs Inversus Viscerum", "Complete situs inversus", "situs inversus viscerum", "complete situs inversus", "Transposition, complete", "Abdominal situs inversus", "Situs inversus visceralis", "situs inversus (diagnosis)", "situs inversus or transversus", "Complete situs inversus viscerum", "All organs on wrong side of body", "complete situs inversus viscerum", "situs inversus totalis (disease)", "Situs inversus viscerum (disorder)", "complete transposition (morphologic abnormality)", "Complete transposition (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "situs inversus", "shortest_name_length": 14}
{"curie": "UMLS:C2103468", "names": ["Optic Chiasm Neoplasm", "neoplasm of optic chiasm", "neoplasm of optic chiasm (diagnosis)", "neoplasm - cranial nerve optic II chiasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplasm of optic chiasm", "shortest_name_length": 21}
{"curie": "UMLS:C0278493", "names": ["Breast cancer recurrent", "breast cancer recurrent", "Recurrent Breast Cancer", "recurrent breast cancer", "breast cancer, recurrent", "Breast Cancer, Recurrent", "Breast carcinoma recurrent", "Carcinoma breast recurrent", "Recurrent Breast Carcinoma", "Breast cancer NOS recurrent", "Breast carcinoma NOS recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast cancer recurrent", "shortest_name_length": 23}
{"curie": "MONDO:0014360", "names": ["DEE21", "EIEE21", "early infantile epileptic encephalopathy 21", "epileptic encephalopathy, early infantile, 21", "developmental and epileptic encephalopathy 21", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 21", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 21", "developmental and epileptic encephalopathy, 21", "NECAP1 early infantile epileptic encephalopathy", "epileptic encephalopathy, early infantile, type 21", "early infantile epileptic encephalopathy caused by mutation in NECAP1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 21", "shortest_name_length": 5}
{"curie": "MONDO:0100316", "names": ["WRS", "RWS", "LQT1", "LQT1 syndrome", "Long QT Syndrome 1", "long QT syndrome 1", "LONG QT SYNDROME 1", "Romano-Ward Syndrome", "Romano-Ward syndrome", "ward-romano syndrome", "Romano Ward syndrome", "Ward Romano Syndrome", "romano ward syndrome", "WARD-ROMANO SYNDROME", "romano-ward syndrome", "Ward-Romano Syndrome", "ROMANO-WARD SYNDROME", "Romano Ward Syndrome", "Syndrome, Ward-Romano", "Syndrome, Romano-Ward", "long QT syndrome type 1", "Long QT Syndrome Type 1", "LQT1 syndrome (diagnosis)", "Romano-Ward long QT syndrome", "long QT syndrome 1/2, digenic", "Romano-Ward syndrome (disorder)", "long QT syndrome 1, acquired, susceptibility to", "LONG QT SYNDROME 1, ACQUIRED, SUSCEPTIBILITY TO", "Ventricular Fibrillation with Prolonged QT Interval", "VENTRICULAR FIBRILLATION WITH PROLONGED QT INTERVAL", "ventricular fibrillation with prolonged QT interval"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "long QT syndrome 1", "shortest_name_length": 3}
{"curie": "UMLS:C0031526", "names": ["Ph1 Chromosome", "Ph 1 Chromosome", "ph 1 chromosome", "Ph1 Chromosomes", "Chromosome, Ph1", "Ph 1 Chromosomes", "Chromosome, Ph 1", "Chromosomes, Ph1", "1 Chromosomes, Ph", "Chromosomes, Ph 1", "chromosome philadelphia", "Philadelphia Chromosome", "Philadelphia chromosome", "philadelphia chromosome", "Chromosome, Philadelphia", "chromosomes philadelphia", "Philadelphia Translocation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Philadelphia Chromosome", "shortest_name_length": 14}
{"curie": "MONDO:0034186", "names": ["autosomal recessive extra-oral halitosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive extra-oral halitosis", "shortest_name_length": 40}
{"curie": "MONDO:0004598", "names": ["Cor pulmonale acute", "Acute cor pulmonale", "acute cor pulmonale", "cor pulmonale, acute", "cor; pulmonale, acute", "Acute cor pulmonale NOS", "acute pulmonary heart disease", "Acute pulmonary heart disease", "Acute cor pulmonale (disorder)", "acute cor pulmonale (diagnosis)", "Acute pulmonary heart disease, NOS", "disease (or disorder); heart, pulmonary, acute"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute cor pulmonale", "shortest_name_length": 19}
{"curie": "UMLS:C1336503", "names": ["Sternal Intraosseous Schwannoma", "Sternal Intraosseous Neurilemmoma", "Intraosseous Schwannoma of Sternum", "Intraosseous Neurilemmoma of Sternum", "Intraosseous Schwannoma of the Sternum", "Intraosseous Neurilemmoma of the Sternum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sternal Intraosseous Schwannoma", "shortest_name_length": 31}
{"curie": "UMLS:C0280415", "names": ["Stage IV Sinonasal Squamous Cell Carcinoma AJCC v7", "Stage IV Nasal Cavity and Paranasal Sinus Squamous Cell Cancer", "Stage IV Nasal Cavity and Paranasal Sinus Squamous Cell Carcinoma", "Stage IV Nasal Cavity and Paranasal Sinus Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Sinonasal Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 50}
{"curie": "MONDO:0008995", "names": ["YVS", "Yunis Varon syndrome", "Yunis-Varón syndrome", "Yunis-Varon syndrome", "YUNIS-VARON SYNDROME", "Yunis-Varon Syndrome", "cleidocranial dysplasia-micrognathia-absent thumbs syndrome", "Cleidocranial dysplasia-micrognathia-absent thumbs syndrome", "Cleidocranial dysplasia, micrognathia, absent thumbs, & distal aphalangia", "cleidocranial dysplasia, micrognathia, absent thumbs, & distal aphalangia", "cleidocranial dysplasia with micrognathia, absent thumbs, and distal Aphalangia", "CLEIDOCRANIAL DYSPLASIA WITH MICROGNATHIA, ABSENT THUMBS, AND DISTAL APHALANGIA", "cleidocranial dysplasia with micrognathia, absent thumbs, and distal aphalangia", "Cleidocranial Dysplasia with Micrognathia, Absent Thumbs, and Distal Aphalangia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Yunis-Varon syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0008321", "names": ["Pruritus, Hereditary Localized", "PRURITUS, HEREDITARY LOCALIZED", "pruritus, hereditary localized"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pruritus, hereditary localized", "shortest_name_length": 30}
{"curie": "MONDO:0033366", "names": ["DEE57", "EIEE57", "infantile epileptic encephalopathy 57", "early infantile epileptic encephalopathy 57", "developmental and epileptic encephalopathy 57", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 57", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 57", "epileptic encephalopathy, early infantile, 57", "developmental and epileptic encephalopathy, 57"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 57", "shortest_name_length": 5}
{"curie": "MONDO:0016271", "names": ["endometrial adenoid cystic carcinoma", "body of uterus adenoid cystic carcinoma", "adenoid cystic carcinoma of the corpus uteri"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenoid cystic carcinoma of the corpus uteri", "shortest_name_length": 36}
{"curie": "MONDO:0014275", "names": ["FRTS3", "EHHADH Fanconi syndrome", "FANCONI RENOTUBULAR SYNDROME 3", "Fanconi renotubular syndrome 3", "Fanconi renotubular syndrome type 3", "Fanconi syndrome caused by mutation in EHHADH"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fanconi renotubular syndrome 3", "shortest_name_length": 5}
{"curie": "UMLS:C0340608", "names": ["a.renalis; thrombosis", "RENAL ARTERY THROMBOSIS", "Renal artery thrombosis", "renal artery thrombosis", "Renal Artery Thrombosis", "thrombosis; renal artery", "artery; renal, thrombosis", "thrombosis; artery, renal", "thrombosis of renal artery", "Thrombosis of renal artery", "Thrombosis of renal artery (disorder)", "thrombosis of renal artery (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thrombosis of renal artery", "shortest_name_length": 21}
{"curie": "UMLS:C5418825", "names": ["Metastatic Rhabdoid Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Rhabdoid Tumor", "shortest_name_length": 25}
{"curie": "MONDO:0012207", "names": ["flat umbilicus familial", "Flat umbilicus familial", "UMBILICUS, FAMILIAL FLAT", "Umbilicus, Familial Flat", "umbilicus, familial flat", "flat umbilicus autosomal dominant", "Flat umbilicus autosomal dominant", "flat umbilicus, autosomal dominant", "FLAT UMBILICUS, AUTOSOMAL DOMINANT", "Flat Umbilicus, Autosomal Dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "umbilicus, familial flat", "shortest_name_length": 23}
{"curie": "UMLS:C0279079", "names": ["adult high grade NHL", "adult NHL, high grade", "NHL, adult high grade", "High Grade Adult Non-Hodgkin's Lymphoma", "high grade non-Hodgkin's lymphoma, adult", "lymphoma, adult high grade non-Hodgkin's", "non-Hodgkin's lymphoma, adult high grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Adult Non-Hodgkin's Lymphoma", "shortest_name_length": 20}
{"curie": "MONDO:0011304", "names": ["CCM2", "cerebral cavernous malformation 2", "Cerebral Cavernous Malformations 2", "cerebral cavernous malformations 2", "CEREBRAL CAVERNOUS MALFORMATIONS 2", "cerebral cavernous malformations-2", "cerebral cavernous malformation type 2", "cerebral cavernous malformations type 2", "CCM2 familial cerebral cavernous malformation", "familial cerebral cavernous malformation caused by mutation in CCM2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral cavernous malformation 2", "shortest_name_length": 4}
{"curie": "MONDO:0008944", "names": ["CPD4", "CORS1", "JBTS1", "Joubert syndrome", "JOUBERT SYNDROME 1", "Joubert syndrome 1", "Joubert syndrome type 1", "INPP5E Joubert syndrome", "Joubert-Boltshauser syndrome", "cerebellooculorenal syndrome 1", "CEREBELLOOCULORENAL SYNDROME 1", "Cerebellooculorenal syndrome 1", "cerebelloparenchymal disorder 4", "cerebelloparenchymal disorder IV", "Joubert syndrome caused by mutation in INPP5E"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome 1", "shortest_name_length": 4}
{"curie": "MONDO:0017871", "names": ["BMAH", "bilateral adrenal hemorrhage", "bilateral massive adrenal hemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bilateral massive adrenal hemorrhage", "shortest_name_length": 4}
{"curie": "MONDO:0002281", "names": ["D22S676", "D22S750", "Anemia macrocytic", "ANEMIA MACROCYTIC", "Macrocytic Anemia", "macrocytic anemia", "anemia macrocytic", "Macrocytic anemia", "macrocytic Anemia", "MACROCYTIC ANEMIA", "Anemia, macrocytic", "Anaemia;macrocytic", "macrocytic anemias", "Macrocytic anaemia", "Anemia, Macrocytic", "Macrocytic Anemias", "anemia; macrocytic", "Anaemia macrocytic", "macrocytic; anemia", "macrocytic anaemia", "ANAEMIA MACROCYTIC", "Anemias, Macrocytic", "Macrocytic anemia NOS", "Macrocytic anaemia NOS", "macrocytic anemia (disease)", "anemia disorders macrocytic", "Macrocytic anemia (disorder)", "macrocytic anemia (diagnosis)", "macrocytic anaemia of unspecified cause"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macrocytic anemia", "shortest_name_length": 7}
{"curie": "UMLS:C0278715", "names": ["Stage V Wilms Tumor", "stage V Wilms tumor", "stage V Wilms' tumor", "Wilms tumor, stage V", "stage V Wilm's tumor", "Wilms' tumor, stage V", "Wilm's tumor, stage V", "stage V nephroblastoma", "nephroblastoma, stage V", "Stage V Renal Wilms Tumor", "Stage V Renal Wilms' Tumor", "Stage V Kidney Wilms Tumor", "Stage V Kidney Nephroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage V Kidney Wilms Tumor", "shortest_name_length": 19}
{"curie": "MONDO:0020375", "names": ["coralliform cataract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coralliform cataract", "shortest_name_length": 20}
{"curie": "MONDO:0032750", "names": ["DA2B2", "distal arthrogryposis type 2B2", "arthrogryposis, distal, type 2B2", "ARTHROGRYPOSIS, DISTAL, TYPE 2B2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis, distal, type 2B2", "shortest_name_length": 5}
{"curie": "MONDO:0001628", "names": ["Nail tinea", "nail tinea", "Nail Fungus", "Fungus, Nail", "tinea unguium", "Tinea unguium", "onychomycoses", "Onychomycoses", "onychomycosis", "Tinea of nail", "ONYCHOMYCOSIS", "Tinea Unguium", "Onychomycosis", "unguium; tinea", "ringworm; nail", "tinea; unguium", "nail; ringworm", "Ringworm of nail", "Ringworm of nails", "OM - Onychomycosis", "nail dermatophytosis", "dermatophytic onychia", "dermatophytosis; nail", "fungal nail infection", "nail; dermatophytosis", "NAIL INFECTION FUNGAL", "Dermatophytic onychia", "cellulitis and abscess", "onychia; dermatophytic", "dermatophytic; onychia", "Dermatophytosis of nail", "infection; fungus, nail", "dermatophytosis of nail", "fungus; infection, nail", "Onychomycosis (disorder)", "fungal infection of nail", "Infection;fungus;nail(s)", "Fungal infection of claw", "Fungal infection of nail", "Nail fungal infection NOS", "dermatophytic onychomycosis", "Fungal infection of nail, NOS", "cellulitis and abscess of face", "Cellulitis and abscess of face", "cellulitis and abscess of trunk", "Cellulitis and abscess of trunk", "Cellulitis and abscess of finger", "cellulitis and abscess of finger", "Cellulitis and abscess of buttock", "cellulitis and abscess of buttock", "Onychomycosis due to dermatophyte", "onychomycosis due to dermatophyte", "dermatophytosis of nail (diagnosis)", "fungal infection of nail (diagnosis)", "Onychomycosis caused by dermatophyte", "cellulitis and abscess of finger and toe", "Cellulitis and abscess of finger and toe", "Cellulitis and abscess of gluteal region", "cellulitis and abscess of gluteal region", "Cellulitis and abscess of face (disorder)", "Cellulitis and abscess of fingers and toes", "Cellulitis and abscess of trunk (disorder)", "cellulitis and abscess of face (diagnosis)", "Cellulitis and abscess of finger (disorder)", "cellulitis and abscess of trunk (diagnosis)", "Cellulitis and abscess of unspecified digit", "Cellulitis and abscess of finger (diagnosis)", "Cellulitis and abscess of buttock (disorder)", "Cellulitis and abscess of buttock (diagnosis)", "Cellulitis and abscess of finger, unspecified", "Onychomycosis caused by dermatophyte (disorder)", "cellulitis and abscess of upper arm and forearm", "cellulitis and abscess of upper extremity finger", "cellulitis and abscess of lower extremity buttock", "Cellulitis and abscess of finger and toe (disorder)", "cellulitis and abscess of finger and toe (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tinea unguium", "shortest_name_length": 10}
{"curie": "MONDO:0012051", "names": ["periodontitis, aggressive, 2", "Periodontitis, Aggressive, 2", "PERIODONTITIS, AGGRESSIVE, 2", "periodontitis, aggressive, type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "periodontitis, aggressive, 2", "shortest_name_length": 28}
{"curie": "MONDO:0004200", "names": ["NMIBC", "Superficial Bladder Cancer", "superficial bladder cancer", "Superficial bladder cancer", "Superficial Bladder Carcinoma", "superficial bladder carcinoma", "carcinoma of bladder, superficial", "Superficial Urinary Bladder Cancer", "superficial urinary bladder cancer", "Non-Muscle Invasive Bladder Cancer", "Non-muscle invasive bladder cancer", "Non-Muscle-Invasive Bladder Cancer", "Cancer, Non-Muscle-Invasive Bladder", "Bladder Cancer, Non-Muscle-Invasive", "Cancers, Non-Muscle-Invasive Bladder", "Bladder Cancers, Non-Muscle-Invasive", "Superficial urinary bladder carcinoma", "superficial urinary bladder carcinoma", "Non-Muscle Invasive Bladder Carcinoma", "Non-Muscle Invasive Bladder Neoplasms", "Non Muscle Invasive Bladder Neoplasms", "Superficial Urinary Bladder Carcinoma", "bladder malignant carcinoma superficial", "Carcinoma of urinary bladder, superficial", "carcinoma of bladder, superficial (diagnosis)", "Carcinoma of urinary bladder, superficial (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "superficial urinary bladder carcinoma", "shortest_name_length": 5}
{"curie": "UMLS:C0161019", "names": ["Stomach FB", "Gastric foreign body", "stomach; foreign body", "foreign body; stomach", "Foreign Body in Stomach", "Foreign body in stomach", "foreign body of stomach", "Gastric foreign body, NOS", "foreign body in the stomach", "Gastric foreign body (diagnosis)", "Foreign body in stomach (disorder)", "foreign body of stomach (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Foreign body in stomach", "shortest_name_length": 10}
{"curie": "UMLS:C2981228", "names": ["Stage II Rectosigmoid Cancer", "Stage II Rectosigmoid Cancer AJCC v6", "Stage II Rectosigmoid Carcinoma AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Rectosigmoid Cancer AJCC v6", "shortest_name_length": 28}
{"curie": "MONDO:0011932", "names": ["HTL", "LAH", "Htl", "Lah1", "LAH1", "HYPT6", "Hypt6", "hypotrichosis 6", "HYPOTRICHOSIS 6", "DSG4 hypotrichosis", "hypotrichosis type 6", "MONILETHRIX-LIKE HYPOTRICHOSIS", "monilethrix-like hypotrichosis", "Monilethrix-like hypotrichosis", "hypotrichosis caused by mutation in DSG4", "autosomal recessive localized hypotrichosis", "hypotrichosis, localized, autosomal recessive", "HYPOTRICHOSIS, LOCALIZED, AUTOSOMAL RECESSIVE", "Hypotrichosis, Localized, Autosomal Recessive", "Hypotrichosis, Localized, Autosomal Recessive 1", "HYPOTRICHOSIS, LOCALIZED, AUTOSOMAL RECESSIVE 1", "hypotrichosis, localized, autosomal recessive 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotrichosis 6", "shortest_name_length": 3}
{"curie": "UMLS:C1262280", "names": ["Hantavirus nephropathy", "Hantavirus Nephropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hantavirus nephropathy", "shortest_name_length": 22}
{"curie": "MONDO:0021132", "names": ["tertiary hyperparathyroidism", "Tertiary Hyperparathyroidism", "Hyperparathyroidism tertiary", "Tertiary hyperparathyroidism", "'tertiary' hyperparathyroidism", "Tertiary hyperparathyroidism (disorder)", "tertiary hyperparathyroidism (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tertiary hyperparathyroidism", "shortest_name_length": 28}
{"curie": "UMLS:C1268964", "names": ["MDS-U", "MDS, U", "Unclassifiable MDS", "Unclassifiable Myelodysplastic Syndrome", "Myelodysplastic syndrome unclassifiable", "Myelodysplastic Syndrome, Unclassifiable", "Myelodysplastic syndrome, unclassifiable"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myelodysplastic syndrome unclassifiable", "shortest_name_length": 5}
{"curie": "MONDO:0013867", "names": ["RTD3", "BVVLS2", "BROWN-Vialetto-VAN Laere syndrome 2", "Riboflavin transporter deficiency 3", "BROWN-VIALETTO-VAN LAERE SYNDROME 2", "brown-Vialetto-van Laere syndrome 2", "Brown-Vialetto-Van Laere Syndrome 2", "Brown-Vialetto-Van Laere syndrome 2", "Brown-Vialetto-Van Laere syndrome type 2", "SLC52A2 Brown-Vialetto-van Laere syndrome", "RFVT3-related riboflavin transporter deficiency", "Brown-Vialetto-van Laere syndrome caused by mutation in SLC52A2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brown-Vialetto-van Laere syndrome 2", "shortest_name_length": 4}
{"curie": "MONDO:0009159", "names": ["EDSCV", "cvEDS", "Cardiac-valvular EDS", "EDS, cardiac valvular type", "Cardiac-valvular Ehlers-Danlos syndrome", "Ehlers-Danlos Syndrome, Arthrochalasis Type", "Ehlers-Danlos syndrome, arthrochalasis type", "Ehlers-Danlos syndrome cardiac valvular type", "Ehlers-Danlos syndrome, CARDIAC valvular type", "Ehlers-Danlos syndrome, cardiac valvular type", "EHLERS-DANLOS SYNDROME, CARDIAC VALVULAR TYPE", "Ehlers-Danlos syndrome, cardiac valvular form", "Cardiac valvular form of Ehlers-Danlos syndrome", "Ehlers-Danlos syndrome cardiac valvular type (disorder)", "Ehlers-Danlos Syndrome, Autosomal Recessive, Cardiac Valvular Form", "Ehlers-Danlos syndrome, autosomal recessive, CARDIAC valvular form", "Ehlers-Danlos syndrome, autosomal recessive, Cardiac valvular form", "Cardiac valvular form of autosomal recessive Ehlers-Danlos syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ehlers-Danlos syndrome, cardiac valvular type", "shortest_name_length": 5}
{"curie": "UMLS:C2111710", "names": ["Bladder Large Cell Neuroendocrine Carcinoma", "large cell neuroendocrine carcinoma of bladder", "large cell neuroendocrine carcinoma of bladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "large cell neuroendocrine carcinoma of bladder", "shortest_name_length": 43}
{"curie": "UMLS:C0156119", "names": ["Gangrenous Umbilical Hernia", "gangrenous umbilical hernia", "Umbilical hernia gangrenous", "Gangrenous umbilical hernia", "Umbilical hernia with gangrene", "hernia; umbilical, with gangrene", "gangrenous umbilical hernia (diagnosis)", "Umbilical hernia with gangrene (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Umbilical hernia with gangrene", "shortest_name_length": 27}
{"curie": "MONDO:0003648", "names": ["tympanic membrane disease", "TYMPANIC MEMBRANE DISORDER", "tympanic membrane disorder", "Tympanic membrane disorder", "disease of tympanic membrane", "DISORDER OF TYMPANIC MEMBRANE", "Disorder of tympanic membrane", "disorder of tympanic membrane", "Tympanic membrane disorder NOS", "disease (or disorder); tympanum", "TM - Tympanic membrane disorder", "DISORDERS OF THE TYMPANIC MEMBRANE", "Disorder of tympanic membrane, NOS", "tympanic membrane disease or disorder", "Disorder of tympanic membrane (disorder)", "disease (or disorder); tympanic membrane", "disease or disorder of tympanic membrane", "disorder of tympanic membrane (diagnosis)", "Unspecified disorder of tympanic membrane", "Disorder of tympanic membrane, unspecified", "Unspecified disorder of tympanic membrane, unspecified ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tympanic membrane disorder", "shortest_name_length": 25}
{"curie": "MONDO:0011409", "names": ["Sm2", "SM2", "hepatic fibrosis susceptibility due to schistosoma mansoni infection", "HEPATIC FIBROSIS, SEVERE, SUSCEPTIBILITY TO, DUE TO SCHISTOSOMA MANSONI INFECTION", "hepatic fibrosis, severe, susceptibility to, due to Schistosoma mansoni infection", "hepatic fibrosis, Severe, susceptibility to, due to Schistosoma japonicum infection", "HEPATIC FIBROSIS, SEVERE, SUSCEPTIBILITY TO, DUE TO SCHISTOSOMA JAPONICUM INFECTION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatic fibrosis, severe, susceptibility to, due to Schistosoma mansoni infection", "shortest_name_length": 3}
{"curie": "MONDO:0004336", "names": ["rectum signet ring cell carcinoma", "rectum signet ring adenocarcinoma", "Signet Ring Adenocarcinoma of Rectum", "signet Ring adenocarcinoma of rectum", "rectal signet ring cell adenocarcinoma", "rectal signet Ring cell adenocarcinoma", "Rectal Signet-Ring Cell Adenocarcinoma", "Rectal Signet Ring Cell Adenocarcinoma", "signet ring adenocarcinoma of the rectum", "signet Ring adenocarcinoma of the rectum", "Signet Ring Adenocarcinoma of the Rectum", "signet Ring cell adenocarcinoma of rectum", "rectal, signet ring adenocarcinoma of the", "adenocarcinoma of the rectum, signet ring", "Signet Ring Cell Adenocarcinoma of Rectum", "rectum, signet ring adenocarcinoma of the", "Signet Ring cell adenocarcinoma of rectum", "Signet Ring Cell Adenocarcinoma of the Rectum", "signet Ring cell adenocarcinoma of the rectum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rectal signet ring cell adenocarcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C0263372", "names": ["Acrodermatitis", "Giannotti-Crosti", "Gianotti-Crosti Syndrome", "Gianotti-Crosti syndrome", "gianotti crosti syndrome", "Gianotti Crosti Syndrome", "gianotti-crosti syndrome", "Syndrome, Gianotti-Crosti", "Acropapulo Vesicular Syndrome", "Acropapulo-Vesicular Syndrome", "Acropapulo-Vesicular Syndromes", "Syndrome, Acropapulo-Vesicular", "Syndromes, Acropapulo-Vesicular", "Acrodermatitis papulosa infantum", "Childhood Papular Acrodermatitis", "Acrodermatitis Papulosa Infantum", "Infantile Papular Acrodermatitis", "Infantile papular acrodermatitis", "infantile papular; acrodermatitis", "Papular Acrodermatitis, Infantile", "acrodermatitis; infantile papular", "Acrodermatitis Papulosa Infantums", "Infantile Papular Acrodermatitides", "Childhood Papular Acrodermatitides", "Gianotti-Crosti syndrome (disorder)", "Papular acrodermatitis of childhood", "Papular Acrodermatitides, Infantile", "Papular Acrodermatitis of Childhood", "Papulovesicular Acrolocated Syndrome", "Gianotti-Crosti syndrome (diagnosis)", "Papulovesicular Acrolocated Syndromes", "Syndromes, Papulovesicular Acrolocated", "Erythemato Vesiculo Papulous Eruptive Syndrome", "Erythemato-Vesiculo-Papulous Eruptive Syndrome", "Syndrome, Erythemato-Vesiculo-Papulous Eruptive", "Erythemato-Vesiculo-Papulous Eruptive Syndromes", "Syndromes, Erythemato-Vesiculo-Papulous Eruptive", "Infantile papular acrodermatitis [Giannotti-Crosti]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gianotti-Crosti Syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C1850600", "names": ["Leigh Syndrome due to Mitochondrial Complex V Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leigh Syndrome due to Mitochondrial Complex V Deficiency", "shortest_name_length": 56}
{"curie": "UMLS:C4329801", "names": ["Euthyroid Condition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Euthyroid Condition", "shortest_name_length": 19}
{"curie": "UMLS:C4324531", "names": ["Intentional dose omission"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intentional dose omission", "shortest_name_length": 25}
{"curie": "UMLS:C5555538", "names": ["Recurrent Diffuse Midline Glioma, H3 K27M-Mutant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Diffuse Midline Glioma, H3 K27M-Mutant", "shortest_name_length": 48}
{"curie": "UMLS:C1333434", "names": ["EBV-Related PTLD", "EBV-Related Post-Transplant Lymphoproliferative Disorder", "Epstein-Barr Virus-Related Post-Transplant Lymphoproliferative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "EBV-Related Post-Transplant Lymphoproliferative Disorder", "shortest_name_length": 16}
{"curie": "UMLS:C5446570", "names": ["Locally Advanced Transitional Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Transitional Cell Carcinoma", "shortest_name_length": 44}
{"curie": "UMLS:C2700132", "names": ["Uterine Cervical Stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Cervical Stenosis", "shortest_name_length": 25}
{"curie": "MONDO:0008447", "names": ["HS", "Sph", "HS1", "SPH", "SPH1", "Spherocytic Anemia", "SPHEROCYTOSIS, TYPE 1", "Spherocytosis, Type 1", "spherocytosis, type 1", "Congenital Spherocytosis", "hereditary spherocytosis 1", "spherocytosis, hereditary, 1", "SPHEROCYTOSIS, HEREDITARY, 1", "Spherocytosis, Hereditary, 1", "ANK1 hereditary spherocytosis", "hereditary spherocytosis type 1", "SPHEROCYTOSIS, TYPE 1 (disorder)", "Congenital Spherocytic Hemolytic Anemia", "hereditary spherocytosis caused by mutation in ANK1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spherocytosis type 1", "shortest_name_length": 2}
{"curie": "UMLS:C4687507", "names": ["Stage II Malignant Thymic Germ Cell Tumor", "Stage II Malignant Mediastinal Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Malignant Mediastinal Germ Cell Tumor", "shortest_name_length": 41}
{"curie": "MONDO:0011522", "names": ["SPG14", "spastic paraplegia 14", "hereditary spastic paraplegia 14", "hereditary spastic paraplegia type 14", "autosomal recessive spastic paraplegia 14", "spastic paraplegia 14, autosomal recessive", "Spastic paraplegia 14, autosomal recessive", "SPASTIC PARAPLEGIA 14, AUTOSOMAL RECESSIVE", "autosomal recessive spastic paraplegia type 14", "Autosomal recessive spastic paraplegia type 14", "Autosomal recessive spastic paraplegia type 14 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 14", "shortest_name_length": 5}
{"curie": "MONDO:0003364", "names": ["gallbladder leiomyosarcoma", "Gallbladder Leiomyosarcoma", "gall bladder leiomyosarcoma", "Leiomyosarcoma of Gallbladder", "leiomyosarcoma of gallbladder", "leiomyosarcoma of gall bladder", "leiomyosarcoma of the gallbladder", "Leiomyosarcoma of the Gallbladder", "leiomyosarcoma of gallbladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gallbladder leiomyosarcoma", "shortest_name_length": 26}
{"curie": "UMLS:C4725629", "names": ["Uveal Melanoma Metastatic in the Liver", "Metastatic Uveal Melanoma in the Liver"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uveal Melanoma Metastatic in the Liver", "shortest_name_length": 38}
{"curie": "UMLS:C5203936", "names": ["Unresectable Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Breast Carcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0011631", "names": ["HFE4", "Ferroportin disease", "ferroportin disease", "Hemochromatosis type 4", "hemochromatosis type 4", "Haemochromatosis type 4", "Hemochromatosis, type 4", "HEMOCHROMATOSIS, TYPE 4", "hemochromatosis, type 4", "SLC40A1 hereditary hemochromatosis", "Hemochromatosis, autosomal dominant", "hemochromatosis, autosomal dominant", "HEMOCHROMATOSIS, AUTOSOMAL DOMINANT", "hemochromatosis due to defect in ferroportin", "HEMOCHROMATOSIS DUE TO DEFECT IN FERROPORTIN", "Hemochromatosis due to defect in ferroportin", "autosomal dominant hereditary hemochromatosis", "Haemochromatosis due to defect in ferroportin", "Autosomal dominant hereditary hemochromatosis", "Autosomal dominant hereditary haemochromatosis", "hereditary hemochromatosis caused by mutation in SLC40A1", "Autosomal dominant hereditary hemochromatosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemochromatosis type 4", "shortest_name_length": 4}
{"curie": "UMLS:C4682807", "names": ["Stage IIIA Testicular Cancer", "Stage IIIA Testicular Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Testicular Cancer AJCC v8", "shortest_name_length": 28}
{"curie": "UMLS:C4763395", "names": ["Recurrent Primary Diffuse Large B-Cell Lymphoma of the Central Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Primary Diffuse Large B-Cell Lymphoma of the Central Nervous System", "shortest_name_length": 77}
{"curie": "EFO:0010819", "names": ["clonal hematopoiesis\"@e"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "clonal hematopoiesis\"@e", "shortest_name_length": 23}
{"curie": "UMLS:C0018134", "names": ["Graft vs Host Reaction", "Graft versus host reaction", "graft versus host reaction", "graft-versus-host reaction", "Graft-versus-host reaction", "GRAFT VERSUS HOST REACTION", "reaction; graft-versus-host", "graft-versus-host; reaction", "graft versus host reactions", "GVH - Graft versus host reaction", "Graft versus host reaction (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Graft vs Host Reaction", "shortest_name_length": 22}
{"curie": "MONDO:0008686", "names": ["ADWH", "wooly", "woolly", "wooly hair", "Wooly hair", "Kinked hair", "Woolly hair", "Wooley hair", "woolly hair", "Afro-textured hair", "Kinky hair texture", "Nappy hair texture", "Frizzy hair syndrome", "Woolly hair syndrome", "woolly hair syndrome", "Congenital wooly hair", "Congenital woolly hair", "Woolly hair, congenital", "Syndrome with woolly hair", "Familial wooly hair syndrome", "familial wooly hair syndrome", "Familial woolly hair syndrome", "familial woolly hair syndrome", "Hereditary wooly hair syndrome", "hereditary wooly hair syndrome", "Hereditary woolly hair syndrome", "hereditary woolly hair syndrome", "woolly hair, autosomal dominant", "Congenital wooly hair (disorder)", "isolated familial woolly hair disorder", "familial woolly hair (autosomal recessive)", "hereditary woolly hair (autosomal dominant)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated familial woolly hair disorder", "shortest_name_length": 4}
{"curie": "UMLS:C0854991", "names": ["Stage I Squamous Cell Lung Cancer", "Lung squamous cell carcinoma stage I", "Stage I Squamous Cell Lung Carcinoma", "Stage I Epidermoid Cell Lung Carcinoma", "Squamous cell carcinoma of lung stage I", "Stage I Squamous Cell Carcinoma of Lung", "Stage I Epidermoid Cell Carcinoma of Lung", "Stage I Squamous Cell Carcinoma of the Lung", "Stage I Squamous Cell Lung Carcinoma AJCC v7", "Stage I Lung Squamous Cell Carcinoma AJCC v7", "Stage I Epidermoid Cell Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung squamous cell carcinoma stage I", "shortest_name_length": 33}
{"curie": "UMLS:C0280167", "names": ["low-grade, stage IV adult NHL", "NHL, low grade, stage IV adult", "adult NHL, stage IV, low grade", "low-grade, metastatic adult NHL", "adult NHL, metastatic, low grade", "NHL, low grade, metastatic adult", "Stage IV Low Grade Adult Non-Hodgkin's Lymphoma", "adult non-Hodgkin's lymphoma, low grade, stage IV", "non-Hodgkin's lymphoma, low grade, stage IV adult", "lymphoma, low grade, stage IV adult non-Hodgkin's", "low-grade, metastatic adult non-Hodgkin's lymphoma", "non-Hodgkin's lymphoma, low grade, metastatic adult", "lymphoma, low grade, metastatic adult non-Hodgkin's", "adult non-Hodgkin's lymphoma, low grade, metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Low Grade Adult Non-Hodgkin's Lymphoma", "shortest_name_length": 29}
{"curie": "MONDO:0014153", "names": ["CORD18", "cone-rod dystrophy 18", "CONE-ROD DYSTROPHY 18", "RAB28 cone-rod dystrophy", "cone-rod dystrophy type 18", "cone-rod dystrophy caused by mutation in RAB28"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cone-rod dystrophy 18", "shortest_name_length": 6}
{"curie": "MONDO:0019145", "names": ["PROC deficiency", "deficiency protein c", "protein c deficiency", "protein C deficiency", "c deficiency protein", "Protein C Deficiency", "Protein C deficiency", "c protein deficiency", "Deficiency, Protein C", "Protein C Deficiencies", "Deficiencies, Protein C", "Reduced protein C activity", "Protein C Deficiency Disease", "Protein C deficiency disease", "protein C deficiency (diagnosis)", "Protein C deficiency disease (disorder)", "hereditary thrombophilia due to PC deficiency", "Thrombophilia, hereditary, due to pc deficiency", "Hereditary Thrombophilia Due To Protein C Deficiency", "autosomal recessive thrombophilia due to PC deficiency", "Congenital thrombotic disease, due to Protein C deficiency", "hereditary thrombophilia due to congenital protein C deficiency", "severe hereditary thrombophilia due to congenital protein C deficiency", "autosomal recessive thrombophilia due to congenital protein C deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary thrombophilia due to congenital protein C deficiency", "shortest_name_length": 15}
{"curie": "MONDO:0010703", "names": ["OCTD", "OTCD", "octd", "OTC Deficiency", "OCT deficiency", "OTC deficiency", "OTC DEFICIENCY", "Deficiency, OTC", "OTC Deficiencies", "Deficiencies, OTC", "valproate sensitivity", "hyperammonemic syndrome", "ORNITHINE TRANSCARBAMYLASE DEFICIENCY", "ornithine transcarbamylase deficiency", "Ornithine transcarbamylase deficiency", "Ornithine Transcarbamylase Deficiency", "deficiency of citrulline phosphorylase", "Ornithine transcarbamoylase deficiency", "deficiency; ornithine transcarbamylase", "Deficiency of citrulline phosphorylase", "Deficiency, Ornithine Transcarbamylase", "ornithine transcarbamylase; deficiency", "Ornithine Transcarbamylase Deficiencies", "Deficiencies, Ornithine Transcarbamylase", "Deficiency of ornithine transcarbamylase", "ornithine carbamoyltransferase deficiency", "Ornithine Carbamoyltransferase Deficiency", "ornithine carbomoyltransferase deficiency", "ORNITHINE CARBAMOYLTRANSFERASE DEFICIENCY", "Ornithine carbamoyltransferase deficiency", "OTC - Ornithine transcarbamylase deficiency", "Deficiency of ornithine carbamoyltransferase", "Ornithine Transcarbamylase Deficiency Disease", "Deficiency Disease, Ornithine Transcarbamylase", "OCT - Ornithine carbamoyltransferase deficiency", "ornithine carbomoyltransferase (OCT) deficiency", "ornithine carbamoyltransferase deficiency (OCTD)", "ornithine carbamoyltransferase deficiency disease", "ornithine transcarbamylase deficiency (diagnosis)", "Ornithine Carbamoyltransferase Deficiency Disease", "Deficiency Disease, Ornithine Carbamoyltransferase", "ornithine transcarbamylase (OTC) deficiency (OTCD)", "Ornithine carbamoyltransferase deficiency (disorder)", "hyperammonemia due to ornithine transcarbamylase deficiency", "ornithine transcarbamylase deficiency, hyperammonemia due to", "ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO", "Ornithine Transcarbamylase Deficiency, Hyperammonemia Due To"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ornithine carbamoyltransferase deficiency", "shortest_name_length": 4}
{"curie": "UMLS:C0751416", "names": ["cancer pelvis", "Pelvis Cancer", "PELVIS CANCER", "pelvis cancer", "cancer pelvic", "pelvic cancer", "Pelvic Cancer", "Pelvis Cancers", "Cancer, Pelvic", "pelvis cancers", "Cancer, Pelvis", "Pelvis--Cancer", "Pelvic Cancers", "Cancers, Pelvis", "Cancers, Pelvic", "cancer of pelvis", "Cancer of Pelvis", "Cancer of the Pelvis", "cancer of the pelvis", "Malignant Pelvic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pelvic Cancer", "shortest_name_length": 13}
{"curie": "MONDO:0021223", "names": ["GI tumor", "GI Tumor", "gut tumor", "GI neoplasm", "GI Neoplasm", "Neoplasia GI", "GI NEOPLASIA", "GI neoplasia", "Tumor of gut", "NEOPLASIA GI", "Tumour of gut", "GI tract tumor", "Digestive Tumor", "digestive tumor", "GI System Tumor", "GI tract tumour", "GI system tumor", "Tumor of GI System", "Digestive Neoplasm", "GI system neoplasm", "digestive neoplasm", "GI System Neoplasm", "tumor of GI system", "neoplasm of GI system", "Neoplasm of GI System", "Digestive System Tumor", "gastrointestinal tumor", "GASTROINTESTINAL TUMOR", "digestive system tumor", "Tumor of the GI System", "tumor of the GI system", "Gastrointestinal Tumor", "Gastrointestinal tumors", "gastrointestinal tumors", "Neoplasm of the GI tract", "digestive system neoplasm", "neoplasm of the GI system", "Tumor of Digestive System", "Digestive System Neoplasm", "Neoplasm of the GI System", "Gastrointestinal Neoplasm", "Gastrointestinal neoplasm", "tumor of digestive system", "gastrointestinal neoplasm", "Neoplasm, Gastrointestinal", "gastrointestinal neoplasms", "Gastrointestinal Neoplasms", "Neoplasms, Gastrointestinal", "Gastrointestinal tract tumor", "neoplasm of digestive system", "Neoplasm of Digestive System", "Gastrointestinal neoplasm NOS", "tumor of the digestive system", "Gastrointestinal tract tumour", "Tumor of the Digestive System", "gastrointestinal tract tumour", "gastrointestinal system tumor", "Gastrointestinal System Tumor", "Gastrointestinal tract neoplasm", "Tumor of gastrointestinal tract", "Gastrointestinal tract neoplasia", "Gastrointestinal System Neoplasm", "Tumor of Gastrointestinal System", "neoplasm of the digestive system", "tumor of gastrointestinal system", "gastrointestinal system neoplasm", "Neoplasm of the Digestive System", "Tumour of gastrointestinal tract", "neoplasm of gastrointestinal tract", "Neoplasm of gastrointestinal tract", "neoplasm of gastrointestinal system", "Neoplasm of Gastrointestinal System", "digestive system neoplasm (disease)", "Tumor of the Gastrointestinal System", "tumor of the gastrointestinal system", "Neoplasm of the gastrointestinal tract", "neoplasm of the gastrointestinal system", "Neoplasm of the Gastrointestinal System", "Neoplasm of gastrointestinal tract (disorder)", "Neoplasm of gastrointestinal tract (diagnosis)", "neoplasm of digestive system gastrointestinal tract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "digestive system neoplasm", "shortest_name_length": 8}
{"curie": "UMLS:C1142169", "names": ["Recurrent Acute Myeloid Leukemia", "Acute myeloid leukemia recurrent", "Acute myeloid leukaemia recurrent", "Recurrent Acute Myeloid Leukemia (AML)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Acute Myeloid Leukemia", "shortest_name_length": 32}
{"curie": "UMLS:C0151874", "names": ["pulmonary mycosis", "PULMONARY MYCOSIS", "Pulmonary mycosis", "Mycosis pulmonary", "fungal infection lung", "lung fungal infection", "Lung infection fungal", "fungal lung infection", "fungal infections lung", "Pulmonary mycosis, NOS", "fungal infection lungs", "fungal infections lungs", "Fungal infection of lung", "fungal infection of lung", "Fungal infection of lung, NOS", "Fungal infection of lung (disorder)", "fungal infection of lung (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fungal infection of lung", "shortest_name_length": 17}
{"curie": "UMLS:C1335031", "names": ["Non-Neoplastic Peritoneal and Retroperitoneal Disease", "Non-Neoplastic Peritoneal and Retroperitoneal Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Peritoneal and Retroperitoneal Disorder", "shortest_name_length": 53}
{"curie": "MONDO:0008312", "names": ["Underbite", "Large jaw", "Prognathia", "Bulldog jaw", "Prognathism", "Big mandible", "Habsburg jaw", "Habsburg Jaw", "Hapsburg Jaw", "macrognathia", "Hapsburg jaw", "Big lower jaw", "Macromandible", "Anteroclusion", "undershot jaw", "Undershot jaw", "Prominent jaw", "'Habsburg jaw'", "'HABSBURG JAW'", "Prominent chin", "'HAPSBURG JAW'", "Large mandible", "'Hapsburg jaw'", "Protrusive chin", "angle class iii", "Angle Class III", "Large lower jaw", "Lower jaw excess", "Enlarged mandible", "Mandibular excess", "mandibular excess", "anterior occlusion", "Prominent mandible", "Anterior occlusion", "Prominent lower jaw", "Mandible prognathism", "Protrusive occlusion", "Mandibular prognathia", "Lower jaw hyperplasia", "prognathism mandibular", "mandibular prognathism", "Mandibular hyperplasia", "mandibular hyperplasia", "Mandibular prognathism", "class iii malocclusion", "Class III malocclusion", "PROGNATHISM, MANDIBULAR", "teeth Angle's class III", "prognathism, mandibular", "Mandibular mesioclusion", "Malocclusion, class III", "Hypertrophy of mandible", "Prognathism, Mandibular", "Enlargement of mandible", "Mandibular macrognathia", "Hyperplasia of lower jaw", "Hypertrophy of lower jaw", "Increased size of mandible", "Increased size of lower jaw", "Malocclusion, Angle Class III", "Malocclusion, Angle class III", "Angle's class III malocclusion", "autosomal dominant prognathism", "Increased size of the mandible", "Class III incisal relationship", "Relative mandibular prognathism", "Malocclusion, Angle's class III", "Increased projection of mandible", "Increased projection of lower jaw", "Mandibular prognathism (disorder)", "mandibular hyperplasia (diagnosis)", "mandibular excess (physical finding)", "Angle's Class III malocclusion of teeth", "Malocclusion, Angle class III (disorder)", "Angle's class III malocclusion (diagnosis)", "Major anomalies of jaw size, mandibular hyperplasia", "Angle's Class III malocclusion of teeth (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant prognathism", "shortest_name_length": 9}
{"curie": "MONDO:0030006", "names": ["COXPD40", "QRSL1-related COXPD", "combined oxidative phosphorylation deficiency 40", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 40", "QRSL1-related combined oxidative phosphorylation defect", "Glutaminyl-transfer ribonucleic acid amidotransferase subunit-related combined oxidative phosphorylation defect", "Glutaminyl-transfer ribonucleic acid amidotransferase subunit-related combined oxidative phosphorylation defect (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation deficiency 40", "shortest_name_length": 7}
{"curie": "UMLS:C0016808", "names": ["Functional Disorder of PMNs", "Functional disorder of polymorphonuclear neutrophil", "Functional Disorder of Polymorphonuclear Neutrophils", "functional disorder of polymorphonuclear neutrophils", "Functional disorders of polymorphonuclear neutrophils", "Functional disorder of polymorphonuclear neutrophil (disorder)", "functional disorder of polymorphonuclear neutrophils (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Functional disorder of polymorphonuclear neutrophil", "shortest_name_length": 27}
{"curie": "MONDO:0000179", "names": ["NLS", "Neu-Laxova syndrome", "Neu-Laxova Syndrome", "neu-laxova syndrome", "Neu Laxova syndrome", "NEU-LAXOVA SYNDROME", "neu laxova syndrome", "NLS - Neu-Laxova syndrome", "Nuclear Localization Signal", "nuclear localization signal", "Neu-Laxova syndrome (disorder)", "3-phosphoglycerate dehydrogenase deficiency neonatal form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neu-Laxova syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0006813", "names": ["Dermal Nevus", "Dermal nevus", "dermal Nevus", "dermal nevus", "Dermal naevus", "Cellular nevus", "Cellular naevus", "Intradermal Nevi", "intradermal nevi", "Intradermal Nevus", "Nevi, Intradermal", "intradermal nevus", "Intradermal nevus", "Naevus;intradermal", "Nevus, Intradermal", "Intradermal naevus", "intradermal naevus", "Dermal cellular nevus", "Dermal cellular naevus", "IDN - Intradermal nevus", "IDN - Intradermal naevus", "intradermal melanocytic nevus", "Intradermal melanocytic nevus", "Intradermal melanocytic naevus", "Dermal cellular nevus (disorder)", "Intradermal nevus (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intradermal nevus", "shortest_name_length": 12}
{"curie": "MONDO:0000115", "names": ["Arnold-Chiari", "Chiari malformation", "Chiari Malformation", "chiari malformation", "chiari malformations", "Arnold Chiari Syndrome", "Arnold-Chiari Syndrome", "arnold-chiari syndrome", "ARNOLD-CHIARI SYNDROME", "arnold chiari syndrome", "Arnold-Chiari syndrome", "arnold-chiari deformity", "Arnold-Chiari Deformity", "arnold chiari deformity", "Arnold-Chiari deformity", "Arnold Chiari Deformity", "Syndrome, Arnold-Chiari", "Deformity, Arnold-Chiari", "Arnold-Chiari; obstruction", "Arnold-Chiari Malformation", "Arnold Chiari Malformation", "Arnola-Chiari malformation", "Arnold-Chiari malformation", "ARNOLD-CHIARI MALFORMATION", "arnold chiari malformation", "obstruction; Arnold-Chiari", "ARNOLD CHIARI MALFORMATION", "arnold-chiari malformation", "Malformation, Arnold-Chiari", "arnold chiari malformations", "Malformation, Arnold Chiari", "(Arnold) Chiari malformation", "(Arnold) Chiari Malformation", "Chiari malformation (disorder)", "Chiari malformation (diagnosis)", "ACM - Arnold-Chiari malformation", "CEREBELLOMEDULLARY MALFORMATION SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chiari malformation", "shortest_name_length": 13}
{"curie": "UMLS:C0242461", "names": ["Nonthrombopenic Purpura", "Nonthrombopenic Purpuras", "Purpura, Nonthrombopenic", "Purpuras, Nonthrombopenic", "Nonthrombocytopenic Purpura", "nonthrombocytopenic purpura", "purpura nonthrombocytopenic", "Purpura, Nonthrombocytopenic", "nonthrombocytopenic purpuras", "purpura; nonthrombocytopenic", "Purpura non-thrombocytopenic", "Non-thrombocytopenic purpura", "nonthrombocytopenic; purpura", "nonthrombocytopenic purpura (diagnosis)", "Non-thrombocytopenic purpura (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Purpura, Nonthrombocytopenic", "shortest_name_length": 23}
{"curie": "UMLS:C1333600", "names": ["Familial Cancer", "familial cancer", "Hereditary Cancer", "Familial Malignant Neoplasm", "Hereditary Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hereditary Malignant Neoplasm", "shortest_name_length": 15}
{"curie": "UMLS:C2826613", "names": ["Small Lymphocytic Lymphoma Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Lymphocytic Lymphoma Variant", "shortest_name_length": 34}
{"curie": "UMLS:C4764277", "names": ["Unresectable Urethral Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Urethral Urothelial Carcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0025712", "names": ["HAE4", "ANGIOEDEMA, HEREDITARY, 4", "angioedema, hereditary, 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angioedema, hereditary, 4", "shortest_name_length": 4}
{"curie": "MONDO:0004166", "names": ["hereditary fallopian tube cancer", "Hereditary Fallopian Tube Cancer", "familial fallopian tube carcinoma", "familiar fallopian tube carcinoma", "Familial Fallopian Tube Carcinoma", "Hereditary Fallopian Tube Carcinoma", "hereditary fallopian tube carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary fallopian tube carcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C0549379", "names": ["Relapsed Cancer", "Recurrent cancer", "Recurrent Cancer", "cancer recurrent", "CANCER RECURRENT", "RECURRENT CANCER", "recurrent cancer", "Relapsed Carcinoma", "Recurrent Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Carcinoma", "shortest_name_length": 15}
{"curie": "MONDO:0005964", "names": ["sinusitis sphenoid", "sphenoid sinusitis", "Sphenoid Sinusitis", "Sinusitis, Sphenoid", "Sphenoidal sinusitis", "Sphenoidal Sinusitis", "Sphenoid Sinusitides", "sphenoidal sinusitis", "Sinusitides, Sphenoid", "Sinusitis, Sphenoidal", "sphenoidal; sinusitis", "sinusitis; sphenoidal", "Sphenoidal Sinusitides", "Sinusitides, Sphenoidal", "sphenoid bone sinusitis", "Sphenoidal sinusitis NOS", "Sphenoidal sinusitis, NOS", "sinusitis of sphenoid bone", "Sphenoidal sinusitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sphenoid sinusitis", "shortest_name_length": 18}
{"curie": "UMLS:C5556453", "names": ["Uterine Corpus Spindle STUMP", "Uterine Corpus Spindle Smooth Muscle Tumor of Uncertain Malignant Potential"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Corpus Spindle Smooth Muscle Tumor of Uncertain Malignant Potential", "shortest_name_length": 28}
{"curie": "MONDO:0054817", "names": ["HLD17", "hypomyelinating leukodystrophy 17", "LEUKODYSTROPHY, HYPOMYELINATING, 17", "leukodystrophy, hypomyelinating, 17"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukodystrophy, hypomyelinating, 17", "shortest_name_length": 5}
{"curie": "UMLS:C0435001", "names": ["ligament injury", "injury ligament", "Ligament Injury", "Ligament injury", "injuries ligament", "Ligament Injuries", "injury of ligament", "Damage To Ligament", "injuries ligaments", "Ligament injury NOS", "Damage to Ligament(s)", "Ligament injury (disorder)", "injury ligament (diagnosis)", "injury of ligament (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ligament injury", "shortest_name_length": 15}
{"curie": "MONDO:0001191", "names": ["leeches", "Leeches", "Leeches, NOS", "Hirudiniasis", "hirudiniasis", "Leech infestation", "leech infestation", "Hirudiniasis, NOS", "infestation; leeches", "leeches; infestation", "Leech infestation NOS", "Leech infestation, NOS", "infestation by leeches", "Hirudinea infectious disease", "Leech infestation (disorder)", "Hirudinea disease or disorder", "Hirudiniasis - leech infestation", "infestation by leeches (diagnosis)", "Hirudinea caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hirudiniasis", "shortest_name_length": 7}
{"curie": "MONDO:0023528", "names": ["KICS", "KSHV Inflammatory Cytokine Syndrome", "KSHV inflammatory cytokine syndrome", "Kaposi sarcoma inflammatory cytokine syndrome", "Kaposi-sarcoma Associated Herpesvirus (KSHV) Inflammatory Cytokine Syndrome", "Kaposi-sarcoma associated Herpesvirus (KSHV) inflammatory cytokine syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "KSHV inflammatory cytokine syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0017723", "names": ["adult Sandhoff disease", "Sandhoff disease of adults", "Sandhoff disease, adult form", "adult GM2 gangliosidosis 0 variant", "Hexosaminidases A and B deficiency, adult form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sandhoff disease, adult form", "shortest_name_length": 22}
{"curie": "MONDO:0003773", "names": ["intracerebral cystic meningioma", "Intracerebral Cystic Meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intracerebral cystic meningioma", "shortest_name_length": 31}
{"curie": "UMLS:C1335726", "names": ["Refractory Mature B-Cell Neoplasm", "Refractory Mature B-Cell Lymphoma", "Refractory Mature B-Cell Non-Hodgkin Lymphoma", "Refractory Mature B-Cell Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Mature B-Cell Non-Hodgkin Lymphoma", "shortest_name_length": 33}
{"curie": "MONDO:0001457", "names": ["Secondary vitreoretinal degeneration", "secondary vitreoretinal degeneration", "Secondary vitreoretinal degenerations", "Secondary vitreoretinal degeneration (disorder)", "secondary vitreoretinal degeneration (diagnosis)", "secondary vitreoretinal peripheral retinal degeneration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary vitreoretinal degeneration", "shortest_name_length": 36}
{"curie": "MONDO:0002274", "names": ["paraproteinaemia", "Monoclonal Paraproteinemia", "monoclonal paraproteinemia", "Monoclonal paraproteinemia", "paraproteinemia monoclonal", "paraproteinemia; monoclonal", "monoclonal paraproteinaemia", "Monoclonal paraproteinaemia", "monoclonal; paraproteinemia", "monoclonal paraproteinemia disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "monoclonal paraproteinemia disease", "shortest_name_length": 16}
{"curie": "UMLS:C0242151", "names": ["violent", "VIOLENT", "Violent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Violent", "shortest_name_length": 7}
{"curie": "MONDO:0012926", "names": ["Ai2a2", "AI2A2", "MMP20 amelogenesis imperfecta", "amelogenesis imperfecta type IIA2", "amelogenesis imperfecta, type IIA2", "amelogenesis imperfecta hypomaturation type 2A2", "amelogenesis imperfecta hypomaturation type IIA2", "amelogenesis imperfecta, hypomaturation type, IIA2", "Amelogenesis Imperfecta, Hypomaturation Type, Iia2", "AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA2", "amelogenesis imperfecta caused by mutation in MMP20", "amelogenesis imperfecta pigmented hypomaturation type 2", "amelogenesis imperfecta, pigmented hypomaturation type, 2", "AMELOGENESIS IMPERFECTA, PIGMENTED HYPOMATURATION TYPE, 2", "Amelogenesis Imperfecta, Pigmented Hypomaturation Type, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amelogenesis imperfecta hypomaturation type 2A2", "shortest_name_length": 5}
{"curie": "UMLS:C4054402", "names": ["Nephropathy due to Tacrolimus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephropathy due to Tacrolimus", "shortest_name_length": 29}
{"curie": "UMLS:C0151966", "names": ["ULCER BLEEDING DUODENAL", "Ulcer bleeding duodenal", "bleeding duodenal ulcer", "duodenal bleeding ulcer", "Duodenal ulcer bleeding", "Bleeding duodenal ulcer", "duodenal ulcer bleeding", "Ulcer duodenal hemorrhage", "DUODENAL ULCER HEMORRHAGE", "Duodenal Ulcer Hemorrhage", "Duodenal ulcer hemorrhage", "ULCER DUODENAL HEMORRHAGE", "duodenal ulcer hemorrhage", "DUODENAL ULCER HEMORRHAGIC", "Ulcer duodenal haemorrhage", "Duodenal ulcer hemorrhagic", "Bleeding of duodenal ulcer", "Duodenal ulcer haemorrhage", "Duodenal ulcer haemorrhagic", "DUODENAL ULCER HAEMORRHAGIC", "DUODENAL ULCER WITH HEMORRHAGE", "Duodenal ulcer with hemorrhage", "Duodenal ulcer with haemorrhage", "Duodenal ulcer, NOS with hemorrhage", "Duodenal ulcer, NOS with haemorrhage", "peptic ulcer duodenal with hemorrhage", "Duodenal ulcer with hemorrhage (disorder)", "Duodenal ulcer with hemorrhage (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Duodenal ulcer with hemorrhage", "shortest_name_length": 23}
{"curie": "UMLS:C1557971", "names": ["Vas Deferens Obstruction", "Vas deferens obstruction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vas deferens obstruction", "shortest_name_length": 24}
{"curie": "UMLS:C3897532", "names": ["Stage IIIA Primary Peritoneal Cancer", "Stage IIIA Primary Peritoneal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Primary Peritoneal Cancer AJCC v7", "shortest_name_length": 36}
{"curie": "UMLS:C0854818", "names": ["Refractory Adult T-Cell Leukemia/Lymphoma", "Adult T-Cell Lymphoma/Leukemia Refractory", "Adult T-cell lymphoma/leukemia refractory", "Refractory Adult T-Cell Lymphoma/Leukemia", "Adult T-cell lymphoma/leukaemia refractory"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult T-cell lymphoma/leukemia refractory", "shortest_name_length": 41}
{"curie": "MONDO:0000386", "names": ["GINET", "GEP-NET", "digestive system NET", "Gastrointestinal NET", "Digestive System NET", "gastrointestinal NET", "Gastroenteropancreatic NET", "gastroenteropancreatic NET", "gastrointestinal neuroendocrine tumor", "Digestive System Neuroendocrine Tumor", "Gastrointestinal Neuroendocrine Tumor", "digestive system neuroendocrine tumor", "gastrointestinal neuroendocrine tumour", "gastrointestinal neuroendocrine tumors", "Gastroenteropancreatic Neuroendocrine Tumor", "gastroenteropancreatic neuroendocrine tumor", "gastrointestinal system neuroendocrine tumor", "Gastrointestinal System Neuroendocrine Tumor", "malignant gastrointestinal neuroendocrine tumor", "malignant gastrointestinal neuroendocrine tumour", "digestive system neuroendocrine tumor, grade 1/2", "Digestive System Well Differentiated Neuroendocrine Tumor", "digestive system well differentiated neuroendocrine tumor", "alimentary part of gastrointestinal system neuroendocrine tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "digestive system neuroendocrine tumor, grade 1/2", "shortest_name_length": 5}
{"curie": "UMLS:C1519923", "names": ["Gartner Duct Adenocarcinoma", "Vaginal Mesonephric Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Mesonephric Adenocarcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0009643", "names": ["MOCOD", "MOCODA", "MOCOD type A", "Hereditary xanthinuria type 2", "Molybdenum cofactor deficiency", "Hereditary xanthinuria, type 2", "Molybdenum Cofactor Deficiency", "molybdenum cofactor deficiency A", "Deficiency of molybdenum cofactor", "molybdenum cofactor deficiency type A", "Molybdenum Cofactor Deficiency Type A", "Xanthine oxidase-sulfite oxidase deficiency", "Xanthine oxidase-sulphite oxidase deficiency", "Combined molybdoflavoprotein enzyme deficiency", "molybdenum cofactor deficiency complementation group A", "Molybdenum cofactor deficiency complementation group A", "molybdenum cofactor deficiency, complementation group A", "Molybdenum Cofactor Deficiency, Complementation Group A", "MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A", "Combined xanthine oxidase and aldehyde oxidase deficiency", "Combined molybdoflavoprotein enzyme deficiency (disorder)", "molybdenum cofactor deficiency, complementation group type a", "Sulfite oxidase deficiency due to molybdenum cofactor deficiency", "Molybdenum cofactor deficiency complementation group A (disorder)", "sulfite oxidase deficiency due to molybdenum cofactor deficiency type A", "Combined xanthine oxidase and sulfite oxidase and aldehyde oxidase deficiency", "Combined xanthine oxidase and sulphite oxidase and aldehyde oxidase deficiency", "Combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase", "SULFITE OXIDASE, XANTHINE DEHYDROGENASE, AND ALDEHYDE OXIDASE, COMBINED DEFICIENCY OF", "sulfite oxidase, xanthine dehydrogenase, and aldehyde oxidase, combined deficiency of", "combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sulfite oxidase deficiency due to molybdenum cofactor deficiency type A", "shortest_name_length": 5}
{"curie": "MONDO:0009534", "names": ["lymphoblastic transformation, inhibition of", "LYMPHOBLASTIC TRANSFORMATION, INHIBITION OF", "Lymphoblastic Transformation, Inhibition of", "chronic mucocutaneous candidiasis due to inhibition of lymphoblastic transformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic mucocutaneous candidiasis due to inhibition of lymphoblastic transformation", "shortest_name_length": 43}
{"curie": "MONDO:0033005", "names": ["GAMOS1", "SCAR5, FORMERLY", "Galloway syndrome", "GALLOWAY-MOWAT SYNDROME 1", "Galloway-Mowat syndrome 1", "nephrosis-microcephaly syndrome", "nephrosis-neuronal dysmigration syndrome", "spinocerebellar ataxia, autosomal recessive 5", "microcephaly, hiatal hernia and nephrotic syndrome", "microcephaly, hiatal hernia, and nephrotic syndrome", "spinocerebellar ataxia, autosomal recessive 5, formerly", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 5, FORMERLY", "cerebellar ataxia with mental retardation, optic atrophy, and skin abnormalities", "cerebellar ataxia with intellectual disability, optic atrophy, and skin abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Galloway-Mowat syndrome 1", "shortest_name_length": 6}
{"curie": "MONDO:0012416", "names": ["DEVRIENDT SYNDROME", "Devriendt syndrome", "severe short stature, hyperphalangy of the index fingers, mental retardation and facial dysmorphism", "severe short stature, hyperphalangy of the index fingers, intellectual disability and facial dysmorphism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Devriendt syndrome", "shortest_name_length": 18}
{"curie": "MONDO:0008451", "names": ["HMN1", "HMN 1", "DHMN1", "HMN I", "dHMN1", "spinal Charcot-Marie-Tooth disease 1", "Charcot-Marie-Tooth disease, spinal, 1", "Charcot-Marie-Tooth disease, spinal, I", "Charcot-Marie-Tooth Disease, Spinal, I", "CHARCOT-MARIE-TOOTH DISEASE, SPINAL, I", "distal hereditary motor neuropathy type I", "distal hereditary motor neuropathy type 1", "Distal hereditary motor neuropathy type 1", "distal hereditary motor neuronopathy type I", "distal hereditary motor neuronopathy type 1", "neuropathy, distal hereditary motor, type 1", "Neuropathy, Distal Hereditary Motor, Type I", "NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE I", "Distal Hereditary Motor Neuronopathy Type I", "neuronopathy, distal hereditary motor, type 1", "neuronopathy, distal hereditary motor, type I", "Neuronopathy, Distal Hereditary Motor, Type I", "NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE I", "Distal hereditary motor neuropathy type 1 (disorder)", "distal hereditary motor neuropathy type 1 (diagnosis)", "SPINAL MUSCULAR ATROPHY, DISTAL, JUVENILE, AUTOSOMAL DOMINANT, I", "Spinal Muscular Atrophy, Distal, Juvenile, Autosomal Dominant, I", "spinal muscular atrophy, distal, juvenile, autosomal dominant, 1", "Autosomal dominant distal juvenile spinal muscular atrophy type 1", "autosomal dominant distal juvenile spinal muscular atrophy type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuronopathy, distal hereditary motor, type 1", "shortest_name_length": 4}
{"curie": "UMLS:C0270075", "names": ["perinatal disease", "Perinatal disorder", "Perinatal Disorder", "diseases perinatal", "DISORDER PERINATAL", "PERINATAL DISORDER", "Perinatal condition", "nos perinatal disease", "Perinatal disease, NOS", "Perinatal disorder (disorder)", "fetal conditions originating in the perinatal period", "Condition in fetus originating in the perinatal period", "condition in fetus originating in the perinatal period", "Condition in foetus originating in the perinatal period", "Unspecified condition originating in the perinatal period", "Condition originating in the perinatal period, unspecified", "FETAL OR NEWBORN CONDITIONS ARISING IN THE PERINATAL PERIOD", "Condition in fetus originating in the perinatal period, NOS", "Condition in foetus originating in the perinatal period, NOS", "Condition in fetus originating in the perinatal period (disorder)", "condition in fetus originating in the perinatal period (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perinatal disorder", "shortest_name_length": 17}
{"curie": "UMLS:C0392106", "names": ["hepatic artery thrombosis", "Hepatic artery thrombosis", "thrombosis; artery, hepatic", "artery; hepatic, thrombosis", "Hepatic artery thrombosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatic artery thrombosis", "shortest_name_length": 25}
{"curie": "MONDO:0002082", "names": ["endocrine tumor", "Endocrine Tumor", "endocrine neoplasm", "Endocrine Neoplasm", "endocrine gland tumor", "Endocrine System Tumor", "endocrine system tumor", "endocrine gland neoplasm", "tumor of endocrine gland", "Endocrine System Neoplasm", "endocrine system neoplasm", "malignant endocrine tumor", "neoplasm of endocrine gland", "endocrine gland neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endocrine gland neoplasm", "shortest_name_length": 15}
{"curie": "MONDO:0019387", "names": ["macrostomia-preauricular tags-external ophthalmoplegia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macrostomia-preauricular tags-external ophthalmoplegia syndrome", "shortest_name_length": 63}
{"curie": "MONDO:0037871", "names": ["amino acidopathy", "amino acid disorder", "amino acid metabolism disease", "amino acid metabolism disorder", "Amino Acid Metabolism Disorder", "disorder of amino acid metabolism", "Disorder of Amino Acid Metabolism", "cellular amino acid metabolic process disease", "disorder of cellular amino acid metabolic process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amino acid metabolism disease", "shortest_name_length": 16}
{"curie": "UMLS:C1336356", "names": ["Stage IVA Oropharynx Epidermoid Carcinoma", "Stage IVA Oropharyngeal Epidermoid Carcinoma", "Stage IVA Epidermoid Carcinoma of Oropharynx", "Stage IVA Oropharynx Squamous Cell Carcinoma", "Stage IVA Squamous Cell Carcinoma of Oropharynx", "Stage IVA Oropharyngeal Squamous Cell Carcinoma", "Stage IVA Epidermoid Carcinoma of the Oropharynx", "Stage IVA Squamous Cell Carcinoma of the Oropharynx", "Stage IVA Oropharyngeal Throat Squamous Cell Cancer", "Stage IVA Oropharyngeal Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Oropharyngeal Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 41}
{"curie": "UMLS:C5419484", "names": ["Cutaneous Acute GvHD", "Acute Cutaneous GvHD", "Acute Cutaneous Graft versus Host Disease", "Cutaneous Acute Graft versus Host Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous Acute Graft versus Host Disease", "shortest_name_length": 20}
{"curie": "UMLS:C4288038", "names": ["Vaginal Myofibroblastoma", "Vaginal Superficial Myofibroblastoma", "Superficial Myofibroblastoma of the Lower Female Genital Tract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Superficial Myofibroblastoma", "shortest_name_length": 24}
{"curie": "UMLS:C0851647", "names": ["Muscle tone disorder", "disorder; muscle tone", "muscle tone; disorder", "Muscle tone abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Muscle tone disorder", "shortest_name_length": 20}
{"curie": "UMLS:C1335438", "names": ["Polyclonal Polymorphic Post-Transplant Lymphoproliferative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Polyclonal Polymorphic Post-Transplant Lymphoproliferative Disorder", "shortest_name_length": 67}
{"curie": "UMLS:C5420818", "names": ["Locally Advanced Cervical Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Cervical Squamous Cell Carcinoma", "shortest_name_length": 49}
{"curie": "MONDO:0002657", "names": ["Mastopathy", "mastopathy", "BREAST DISEASE", "Breast Disease", "breast disease", "Breast disease", "breast disorder", "Breast Diseases", "BREAST DISORDER", "Breast disorder", "breast diseases", "Breast Disorder", "Disease, Breast", "BREAST DISORDERS", "Breast disorders", "mammary disorder", "Diseases, Breast", "Breast--Diseases", "breast disorders", "disease of breast", "Disease of breast", "Disorder of breast", "diseases of breast", "disorder of breast", "Diseases of Breast", "DISORDERS OF BREAST", "Disorders of breast", "Breast disorder NOS", "Disease of breast, NOS", "diseases of the breast", "DISEASES OF THE BREAST", "Disorder of breast, NOS", "breast disease or disorder", "Unspecified breast disorder", "breast disorders (diagnosis)", "disease or disorder of breast", "Disorder of breast (disorder)", "Disorders of breast (N60-N65)", "Disorder of breast, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast disorder", "shortest_name_length": 10}
{"curie": "MONDO:0014596", "names": ["LIS7", "lissencephaly 7 with cerebellar hypoplasia", "LISSENCEPHALY 7 WITH CEREBELLAR HYPOPLASIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lissencephaly 7 with cerebellar hypoplasia", "shortest_name_length": 4}
{"curie": "UMLS:C0677682", "names": ["Stage I Indolent Non-Hodgkin Lymphoma", "Stage I Indolent Adult Non-Hodgkin Lymphoma", "stage I indolent adult non-Hodgkin lymphoma", "indolent, stage I adult non-Hodgkin lymphoma", "stage I indolent adult non-Hodgkin's lymphoma", "Indolent Stage I Adult Non-Hodgkin's Lymphoma", "Indolent Adult Non-Hodgkin's Lymphoma Stage I", "Stage I Indolent Adult Non-Hodgkin's Lymphoma", "indolent stage I adult non-Hodgkin's lymphoma", "indolent adult non-Hodgkin's lymphoma stage I", "Ann Arbor Stage I Indolent Adult Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Indolent Adult Non-Hodgkin Lymphoma", "shortest_name_length": 37}
{"curie": "UMLS:C0340354", "names": ["Cardiac Q fever", "Q fever endocarditis", "Endocarditis Q fever", "Coxiella endocarditis", "Endocarditis - Q fever", "Coxiella burnetti endocarditis", "Q fever endocarditis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Q fever endocarditis", "shortest_name_length": 15}
{"curie": "MONDO:0020295", "names": ["anomaly pulmonary vein", "Anomalous pulmonary vein", "anomalous pulmonary vein", "Abnormality of lung veins", "Pulmonary vein abnormality", "pulmonary vein abnormality", "Anomaly NOS of pulmonary veins", "PV - Pulmonary vein abnormality", "Abnormality of the pulmonary veins", "congenital pulmonary veins anomaly", "Congenital pulmonary veins anomaly", "congenital anomaly of pulmonary vein", "Congenital anomaly of pulmonary veins", "congenital anomaly of pulmonary veins", "Congenital Anomaly of Pulmonary Veins", "Congenital anomaly of pulmonary veins, NOS", "congenital anomaly of pulmonary vein (diagnosis)", "Congenital anomaly of pulmonary veins (disorder)", "congenital anomaly of pulmonary veins (diagnosis)", "Anomalous pulmonary vein (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital pulmonary veins anomaly", "shortest_name_length": 22}
{"curie": "UMLS:C0279937", "names": ["cancer of the renal pelvis and ureter, metastatic", "Metastatic Upper Urinary Tract Urothelial Carcinoma", "carcinoma of the renal pelvis and ureter, metastatic", "Metastatic Renal Pelvis and Ureter Urothelial Carcinoma", "Renal pelvis and ureter transitional cell cancer metastatic", "Metastatic Urothelial Cancer of the Renal Pelvis and Ureter", "Renal pelvis and ureteric cancer metastatic transitional cell", "Renal pelvis and ureteric cancer transitional cell metastatic", "Renal pelvis and ureteral cancer transitional cell metastatic", "Transitional cell cancer of renal pelvis and ureter metastatic", "Metastatic Urothelial Carcinoma of the Renal Pelvis and Ureter", "Metastatic Transitional Cell Cancer of Renal Pelvis and Ureter", "Metastatic Transitional Cell Carcinoma of Renal Pelvis and Ureter", "metastatic transitional cell cancer of the renal pelvis and ureter", "Metastatic Transitional Cell Cancer of the Renal Pelvis and Ureter", "transitional cell cancer of the renal pelvis and ureter, metastatic", "Malignant neoplasm of renal pelvis and ureter metastatic transitional cell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transitional cell cancer of renal pelvis and ureter metastatic", "shortest_name_length": 49}
{"curie": "MONDO:0003676", "names": ["Inferolateral Myocardial Infarct", "inferolateral myocardial infarct", "Inferolateral Myocardial Infarction by ECG Finding", "Inferolateral Myocardial Infarction by EKG Finding"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inferolateral myocardial infarct", "shortest_name_length": 32}
{"curie": "MONDO:0013286", "names": ["CVID6", "common variable immunodeficiency 6", "immunodeficiency, common variable, 6", "IMMUNODEFICIENCY, COMMON VARIABLE, 6", "CD81 common variable immunodeficiency", "antibody deficiency due to CD81 defect", "ANTIBODY DEFICIENCY DUE TO CD81 DEFECT", "immunodeficiency, common variable, type 6", "common variable immunodeficiency caused by mutation in CD81"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency, common variable, 6", "shortest_name_length": 5}
{"curie": "MONDO:0019142", "names": ["Porphyria", "porphyria", "PORPHYRIA", "Porphyrias", "porphyrias", "Porphyria NOS", "Porphyria, NOS", "Porphyrinopathy", "porphyrinopathy", "Hematoporphyria", "porphyrinopathies", "porphyrin disorder", "Porphyrin Disorder", "Porphyrin Disorders", "Disorder, Porphyrin", "inherited porphyria", "Porphyrinopathy, NOS", "hereditary porphyria", "Porphyria (disorder)", "Disorders, Porphyrin", "porphyria (diagnosis)", "Unspecified porphyria", "Porphyrinopathy (disorder)", "porphyrin; metabolic disorder", "PORPHYRIN METABOLISM DISORDER", "metabolic disorder; porphyrin", "Porphyrin metabolism disorder", "Disorder of porphyrin metabolism", "disorder of porphyrin metabolism", "DISORDERS OF PORPHYRIN METABOLISM", "Disorders of porphyrin metabolism", "disorders of porphyrin metabolism", "Disorders of Porphyrin Metabolism", "Porphyrin metabolism disorder NOS", "Disorder of porphyrin metabolism, NOS", "disorder of porphyrin and hem metabolism", "Disorder of porphyrin and heme metabolism", "disorder of porphyrin and heme metabolism", "Disorder of porphyrin and haem metabolism", "Disorder of porphyrin metabolism (disorder)", "disorder of porphyrin metabolism (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited porphyria", "shortest_name_length": 9}
{"curie": "MONDO:0000236", "names": ["oropharyngeal anthrax", "oropharynx anthrax infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oropharyngeal anthrax", "shortest_name_length": 21}
{"curie": "MONDO:0014656", "names": ["PEOB2", "adult-onset CPEO with mitochondrial myopathy", "autosomal recessive progressive external ophthalmoplegia 2", "progressive external ophthalmoplegia, autosomal recessive 2", "PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE 2", "RNASEH1 progressive external ophthalmoplegia with mitochondrial DNA deletions", "adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy", "autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 2", "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2", "PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 2", "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive type 2", "progressive external ophthalmoplegia with mitochondrial DNA deletions caused by mutation in RNASEH1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2", "shortest_name_length": 5}
{"curie": "UMLS:C2826321", "names": ["RT", "Refractory Thrombocytopenia", "Refractory thrombocytopenia", "thrombocytopenia refractory", "Refractory thrombocytopaenia", "Refractory thrombocytopenia (disorder)", "Refractory thrombocytopenia (diagnosis)", "Refractory thrombocytopenia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Thrombocytopenia", "shortest_name_length": 2}
{"curie": "UMLS:C0399478", "names": ["Smokers keratosis", "Smoker's Keratosis", "Smokers keratosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Smokers keratosis", "shortest_name_length": 17}
{"curie": "MONDO:0009552", "names": ["MDM", "mal de Meleda", "Mal de Meleda", "MAL DE Meleda", "MAL DE MELEDA", "MELEDA DISEASE", "Meleda Disease", "Meleda, Mal de", "de Meleda, Mal", "Meleda disease", "Disease, Meleda", "Acroerythrokeratoderma", "mal de Meleda (diagnosis)", "Acroerythrokeratoderma (disorder)", "keratosis palmoplantaris transgradiens of Siemens", "Keratosis palmoplantaris transgrediens of Siemens", "Keratosis Palmoplantaris Transgradiens of Siemens", "transgrediens palmoplantar keratoderma of Siemens", "KERATOSIS PALMOPLANTARIS TRANSGREDIENS OF SIEMENS", "Transgrediens palmoplantar keratoderma of Siemens", "keratosis palmoplantaris transgrediens of Siemens"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mal de Meleda", "shortest_name_length": 3}
{"curie": "MONDO:0016686", "names": ["astrocytoma diffuse", "Diffuse Astrocytoma", "Diffuse astrocytoma", "diffuse astrocytoma", "Grade 2 Astrocytoma", "grade II astrocytoma", "Astrocytoma, Diffuse", "Grade II Astrocytoma", "astrocytoma, diffuse", "Astrocytoma, Grade II", "Grade II Astrocytomas", "WHO Grade 2 Astrocytoma", "Diffuse Astrocytoma, NOS", "WHO Grade II Astrocytoma", "Grade 2 Astrocytic Tumor", "WHO grade II astrocytoma", "Grade II Astrocytic Tumor", "grade II astrocytic tumor", "Low-grade astrocytoma, NOS", "Grade 2 Astrocytic Neoplasm", "grade II astrocytic neoplasm", "Grade II Astrocytic Neoplasm", "low-grade diffuse astrocytoma", "Pleomorphic Xanthoastrocytoma", "Xanthoastrocytoma, Pleomorphic", "Pleomorphic Xanthoastrocytomas", "Diffuse astrocytoma, low grade", "ASTROCYTOMA, DIFFUSE, MALIGNANT", "astrocytoma, diffuse, malignant", "fibrillary astrocytoma (histologic variant)", "Diffuse Astrocytoma, Not Otherwise Specified", "gemistocytic astrocytoma (histologic variant)", "Diffuse astrocytoma (morphologic abnormality)", "protoplasmic astrocytoma (histologic variant)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diffuse astrocytoma", "shortest_name_length": 19}
{"curie": "MONDO:0011147", "names": ["Deletion 18q", "monosomy 18q", "18q syndrome", "18Q Syndrome", "18q-Syndrome", "deletion 18q", "18Q syndrome", "18q-syndrome", "Monosomy 18q", "18q- Syndrome", "18Q- syndrome", "18q- SYNDROME", "proximal 18q-", "18q- syndrome", "monosomy type 18q", "del(18q) syndrome", "partial monosomy 18q", "monosomy 18q syndrome", "de Grouchy syndrome 2", "18q deletion syndrome", "18q Deletion Syndrome", "proximal 18q deletion", "Deletion 18q Syndrome", "deletion 18q syndrome", "chromosome 18q monosomy", "chromosome 18q deletion", "chromosome 18Q- syndrome", "Chromosome 18q- Syndrome", "CHROMOSOME 18q- SYNDROME", "proximal 18q deletion syndrome", "Chromosome 18 deletion syndrome", "chromosome 18q deletion syndrome", "Chromosome 18q Deletion Syndrome", "CHROMOSOME 18q DELETION SYNDROME", "chromosome; 18 long arm deletion", "partial deletion of chromosome 18q", "partial monosomy of chromosome 18q", "deletions of long arm chromosome 18", "deletion of long arm of chromosome 18", "Deletion of long arm of chromosome 18", "proximal chromosome 18q deletion syndrome", "Deletion of long arm of chromosome 18 (disorder)", "deletion of long arm of chromosome 18 (diagnosis)", "partial deletion of the long arm of chromosome 18", "partial monosomy of the long arm of chromosome 18", "partial deletion of the long arm of chromosome type 18"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 18q deletion syndrome", "shortest_name_length": 12}
{"curie": "UMLS:C4545024", "names": ["Conjunctival Hemangioma", "Conjunctival hemangioma", "Conjunctival haemangioma", "Hemangioma of conjunctiva", "Haemangioma of conjunctiva", "Hemangioma of conjunctiva (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemangioma of conjunctiva", "shortest_name_length": 23}
{"curie": "MONDO:0700088", "names": ["DYT-MR-1", "paroxysmal nonkinesigenic dyskinesia", "Paroxysomal nonkinesigenic dyskinesia", "paroxysmal non-kinesigenic dyskinesia", "Paroxystic non-kinesigenic choreoathetosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paroxysmal nonkinesigenic dyskinesia", "shortest_name_length": 8}
{"curie": "MONDO:0002965", "names": ["fimbrial cyst", "Fimbrial cyst", "cyst; fimbrial", "fimbrial; cyst", "cyst, fimbrial", "cysts fimbrial", "Cyst, fimbrial", "Paratubal cyst", "PAROVARIAN CYST", "Parovarian Cyst", "Paratubal cysts", "parovarian cyst", "cyst, Paratubal", "Parovarian cyst", "parovarian cysts", "cysts, Paratubal", "cyst, parovarian", "Parovarian Cysts", "Cyst, parovarian", "Morgagni hydatid", "Cyst, Parovarian", "Paraovarian cyst", "para-ovarian cyst", "Para-ovarian cyst", "Morgagni Hydatids", "cyst; paraovarian", "paraovarian; cyst", "cysts, parovarian", "Cysts, Parovarian", "hydatid of Morgagni", "Morgagni hydatid cyst", "Morgagni hydatid cysts", "embryonic fimbrial cyst", "Embryonic fimbrial cyst", "hydatid cyst of Morgagni", "Cyst of periovarian tissue", "Cyst of paraovarian tissue", "para-ovarian cyst (diagnosis)", "Cyst of paraovarian tissue (disorder)", "Embryonic cyst of fimbria of fallopian tube", "Congenital cyst of fimbria of fallopian tube", "Embryonic cyst of fimbria of fallopian tube (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parovarian cyst", "shortest_name_length": 13}
{"curie": "UMLS:C4725092", "names": ["Advanced Uveal Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Uveal Melanoma", "shortest_name_length": 23}
{"curie": "UMLS:C0280153", "names": ["Stage II Burkitt Lymphoma", "stage II adult Burkitt lymphoma", "Stage II Adult Burkitt Lymphoma", "Stage II Adult Burkitt's Lymphoma", "Ann Arbor Stage II Adult Burkitt Lymphoma", "stage II adult small noncleaved cell lymphoma", "adult small noncleaved cell lymphoma, stage II", "Adult Diffuse Small Non-Cleaved Cell Lymphoma Stage II", "Stage II Adult Diffuse Small Non-Cleaved Cell Lymphoma", "stage II adult diffuse small noncleaved cell/Burkitt's lymphoma", "Stage II Adult Diffuse Small Non-Cleaved Cell/Burkitt's Lymphoma", "Adult Diffuse Small Non-Cleaved Cell/Burkitt's Lymphoma Stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Adult Burkitt Lymphoma", "shortest_name_length": 25}
{"curie": "UMLS:C0920156", "names": ["Biliary sepsis", "Biliary infection", "Biliary tract infection", "infection biliary tract", "biliary tract infection", "biliary infections tract", "Infection of biliary tract", "Biliary tract infection NOS", "Biliary tract infection (diagnosis)", "Infection of biliary tract (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Biliary tract infection", "shortest_name_length": 14}
{"curie": "MONDO:0009443", "names": ["hi", "HI", "ARCI4B", "harlequin", "HARLEQUIN FETUS", "harlequin fetus", "Harlequin Fetus", "Harlequin fetus", "Fetus, Harlequin", "Harlequin foetus", "fetal; ichthyosis", "'Harlequin fetus'", "'HARLEQUIN FETUS'", "ichthyosis; fetalis", "Harlequin ichthyosis", "Harlequin Ichthyoses", "harlequin ichthyosis", "Harlequin Ichthyosis", "HARLEQUIN ICHTHYOSIS", "Ichthyosis, Harlequin", "Ichthyoses, Harlequin", "Harlequin Baby Syndrome", "Baby Syndrome, Harlequin", "Harlequin Baby Syndromes", "Syndrome, Harlequin Baby", "Harlequin-type ichthyosis", "Syndromes, Harlequin Baby", "Baby Syndromes, Harlequin", "Harlequin type ichthyosis", "Ichthyosis, Harlequin type", "Harlequin fetus (disorder)", "harlequin fetus (diagnosis)", "Harlequin ichthyosis (disorder)", "harlequin type ichthyosis fetalis", "Ichthyosis fetalis, Harlequin type", "ichthyosis fetalis, Harlequin type", "harlequin type ichthyosis congenita", "Ichthyosis congenita, Harlequin type", "ichthyosis congenita, Harlequin type", "Ichthyosis congenita, Harlequin fetus type", "ichthyosis congenita, Harlequin fetus type", "ICHTHYOSIS CONGENITA, HARLEQUIN FETUS TYPE", "autosomal recessive congenital ichthyosis 4B", "ichthyosis, congenital, autosomal recessive 4B", "ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 4B", "autosomal recessive congenital ichthyosis type 4B", "ichthyosis, congenital, autosomal recessive type 4B", "ichthyosis , congenital, autosomal recessive 4b (harlequin)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive congenital ichthyosis 4B", "shortest_name_length": 2}
{"curie": "UMLS:C5238389", "names": ["Advanced Colon Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Colon Carcinoma", "shortest_name_length": 24}
{"curie": "MONDO:0016051", "names": ["Cleft lip retinopathy syndrome", "cleft lip-retinopathy syndrome", "Cleft lip-retinopathy syndrome", "cleft lip-cone rod dystrophy syndrome", "Cleft lip-cone rod dystrophy syndrome", "Ausems-Wittebol Post-Hennekam syndrome", "Ausems Wittebol-Post Hennekam syndrome", "Ausems Wittebol Post Hennekam syndrome", "Cleft lip with progressive retinopathy", "cleft lip with progressive retinopathy", "Cleft lip retinopathy syndrome (disorder)", "cleft lip-progressive retinopathy syndrome", "Cleft lip-progressive retinopathy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleft lip-retinopathy syndrome", "shortest_name_length": 30}
{"curie": "UMLS:C3274465", "names": ["Sickle B+ Thalassemia", "Sickle Beta Plus Thalassemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sickle Beta Plus Thalassemia", "shortest_name_length": 21}
{"curie": "UMLS:C0840926", "names": ["Congenital spondylolysis", "Congenital Spondylolysis", "congenital; spondylolysis", "spondylolysis; congenital"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital spondylolysis", "shortest_name_length": 24}
{"curie": "MONDO:0019629", "names": ["sclerocornea", "Sclerocornea", "sclerocornea (disease)", "isolated congenital sclerocornea", "Hardening of skin and connective tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sclerocornea", "shortest_name_length": 12}
{"curie": "MONDO:0010261", "names": ["MAA2", "ANOP2", "MCOPS2", "OFCD Syndrome", "OFCD syndrome", "OFCD SYNDROME", "MAA2, FORMERLY", "MAA2 (formerly)", "ANOP2, FORMERLY", "ANOP2 (formerly)", "Marashi Gorlin syndrome", "syndromic microphthalmia 2", "Microphthalmia syndromic 2", "microphthalmia syndromic 2", "MICROPHTHALMIA, SYNDROMIC 2", "Microphthalmia, syndromic 2", "microphthalmia, syndromic 2", "Oculofaciocardiodental syndrome", "OCULOFACIOCARDIODENTAL SYNDROME", "syndromic microphthalmia type 2", "oculofaciocardiodental syndrome", "microphthalmia, syndromic type 2", "Oculo-facio-cardio-dental syndrome", "Oculo facio cardio dental syndrome", "Oculofaciocardiodental syndrome (disorder)", "microphthalmia, syndromic 2, X-linked dominant", "Microphthalmia, cataract, radiculomegaly and septal heart defect", "microphthalmia cataracts radiculomegaly and septal heart defects", "Cataracts, microphthalmia, radiculomegaly and septal heart defects", "microphthalmia, cataracts, radiculomegaly, and septal heart defects", "Microphthalmia, cataracts, radiculomegaly, and septal heart defects", "MICROPHTHALMIA, CATARACTS, RADICULOMEGALY, AND SEPTAL HEART DEFECTS", "Cataract-microphthalmia-radiculomegaly-cardiac septal defect syndrome", "cataract-microphthalmia-radiculomegaly-cardiac septal defect syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microphthalmia, syndromic 2", "shortest_name_length": 4}
{"curie": "UMLS:C4520716", "names": ["stage II anal cancer", "Stage II Anal Canal Cancer", "Stage II Anal Canal Cancer AJCC v7", "Stage II Anal Canal Cancer AJCC v6", "Stage II Anal Carcinoma AJCC v6 and v7", "Stage II Anal Canal Cancer AJCC v6 and v7", "Stage II Anal Canal Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Anal Canal Cancer AJCC v6 and v7", "shortest_name_length": 20}
{"curie": "UMLS:C1266004", "names": ["squamous cell carcinoma with horn formation", "Squamous cell carcinoma with horn formation", "Squamous Cell Carcinoma with Horn Formation", "squamous cell carcinoma with horn formation (diagnosis)", "Squamous cell carcinoma with horn formation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Squamous cell carcinoma with horn formation", "shortest_name_length": 43}
{"curie": "MONDO:0010822", "names": ["WARBM", "WARBM1", "Micro syndrome", "micro syndrome", "MICRO SYNDROME", "Micro Syndrome", "micro syndrome 1", "Micro Syndrome 1", "Warburg micro syndrome", "WARBURG MICRO SYNDROME", "WARBURG micro syndrome 1", "Warburg micro syndrome 1", "WARBURG MICRO SYNDROME 1", "Warburg micro syndrome type 1", "Warburg Sjo Fledelius syndrome", "WARBM1 Warburg micro syndrome 1", "RAB3GAP1 Warburg micro syndrome", "Warburg micro syndrome (disorder)", "Warburg micro syndrome (diagnosis)", "Warburg micro syndrome caused by mutation in RAB3GAP1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Warburg micro syndrome 1", "shortest_name_length": 5}
{"curie": "MONDO:0800158", "names": ["inborn disorder of glutamate/glutamine and aspartate/asparagine metabolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of glutamate/glutamine and aspartate/asparagine metabolism", "shortest_name_length": 74}
{"curie": "MONDO:0014553", "names": ["TNORS", "TENORIO SYNDROME", "TENORIO syndrome", "Tenorio syndrome", "OVERGROWTH, MACROCEPHALY, AND INTELLECTUAL DISABILITY SYNDROME", "overgrowth, macrocephaly, and intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tenorio syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0034748", "names": ["Reactive Attachment Disorder of Infancy or Early Childhood", "reactive attachment disorder of infancy or early childhood", "Reactive attachment disorder of infancy or early childhood", "reactive attachment disorder of infancy or early childhood (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reactive attachment disorder of infancy or early childhood", "shortest_name_length": 58}
{"curie": "UMLS:C0279601", "names": ["TdT positive childhood ALL", "ALL, childhood TdT positive", "childhood ALL, TdT positive", "pediatric ALL, TdT positive", "TdT positive ALL, childhood", "ALL, pediatric TdT positive", "ALL, TdT positive, pediatric", "ALL, TdT positive, childhood", "TdT Positive Acute Lymphoblastic Leukemia", "TdT positive pediatric acute lymphocytic leukemia", "TdT positive childhood acute lymphocytic leukemia", "acute lymphocytic leukemia, childhood TdT positive", "TdT positive lymphocytic leukemia, acute childhood", "leukemia, pediatric acute lymphocytic TdT positive", "TdT positive acute lymphocytic leukemia, childhood", "leukemia, childhood acute lymphocytic TdT positive", "TdT positive childhood acute lymphoblastic leukemia", "Childhood TdT Positive Acute Lymphoblastic Leukemia", "acute lymphoblastic leukemia, childhood TdT positive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood TdT Positive Acute Lymphoblastic Leukemia", "shortest_name_length": 26}
{"curie": "UMLS:C0151815", "names": ["Occlusion mesenteric", "Mesenteric occlusion", "occlusion mesenteric", "mesenteric occlusion", "OCCLUSION MESENTERIC", "MESENTERIC OCCLUSION", "OCCLUSION MESENTERIC ARTERY", "mesenteric artery occlusion", "Occlusion mesenteric artery", "occlusion; mesenteric artery", "Mesenteric arterial occlusion", "MESENTERIC ARTERIAL OCCLUSION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mesenteric arterial occlusion", "shortest_name_length": 20}
{"curie": "UMLS:C5206579", "names": ["Testicular Myeloid Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular Myeloid Sarcoma", "shortest_name_length": 26}
{"curie": "MONDO:0021209", "names": ["Heart Tumor", "heart tumor", "Cardiac Tumor", "Cardiac tumor", "Tumor of Heart", "tumor of heart", "Heart neoplasm", "Heart Neoplasm", "heart neoplasm", "Cardiac Neoplasm", "Cardiac neoplasm", "Cardiac Neoplasms", "Neoplasm of Heart", "neoplasm of heart", "Cardiac neoplasms", "Tumor of the Heart", "tumor of the heart", "Intracavitary tumors", "neoplasm of the heart", "Neoplasm of the Heart", "heart neoplasm (disease)", "primary cardiac tumors, childhood", "myocardial tumors (rhabdomyomas and fibromas)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heart neoplasm", "shortest_name_length": 11}
{"curie": "UMLS:C4521612", "names": ["Stage IA Pleural Malignant Mesothelioma", "Stage IA Pleural Malignant Mesothelioma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Pleural Malignant Mesothelioma AJCC v8", "shortest_name_length": 39}
{"curie": "UMLS:C4684847", "names": ["Lung Myoepithelioma", "Benign Lung Myoepithelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Myoepithelioma", "shortest_name_length": 19}
{"curie": "MONDO:0100018", "names": ["adult onset PRP", "adult onset pityriasis rubra pilaris"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult onset pityriasis rubra pilaris", "shortest_name_length": 15}
{"curie": "UMLS:C4511057", "names": ["Congenital myopathy Paradas type", "Congenital myopathy, Paradas type", "Congenital muscular dystrophy Paradas type", "Congenital muscular dystrophy Paradas type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital muscular dystrophy Paradas type", "shortest_name_length": 32}
{"curie": "MONDO:0009685", "names": ["MM", "MMD1", "Miyoshi myopathy", "MIYOSHI MYOPATHY", "Miyoshi myopathy 1", "Miyoshi distal myopathy", "Miyoshi muscular dystrophy", "Miyoshi muscular dystrophy 1", "MIYOSHI MUSCULAR DYSTROPHY 1", "Miyoshi Muscular Dystrophy 1", "Miyoshi muscular dystrophy type 1", "MUSCULAR DYSTROPHY, DISTAL, LATE-ONSET, AUTOSOMAL RECESSIVE", "muscular dystrophy, distal, late onset, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Miyoshi myopathy", "shortest_name_length": 2}
{"curie": "MONDO:0013907", "names": ["MSSP", "PMGYS", "polymicrogyria with seizures", "POLYMICROGYRIA WITH SEIZURES", "bilateral generalized polymicrogyria", "bilateral generalised polymicrogyria", "microcephaly, short stature, and polymicrogyria with seizures", "MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH OR WITHOUT SEIZURES", "microcephaly, short stature, and polymicrogyria with or without seizures", "Microcephalic cortical malformations-short stature due to RTTN deficiency", "Microcephalic cortical malformations, short stature due to RTTN deficiency", "Microcephalic cortical malformations, short stature due to rotatin deficiency", "Microcephalic cortical malformations, short stature due to RTTN (rotatin) deficiency", "Microcephalic cortical malformations, short stature due to rotatin deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bilateral generalized polymicrogyria", "shortest_name_length": 4}
{"curie": "MONDO:0007298", "names": ["ACV", "CNPCA", "SCA29", "spinocerebellar ataxia 29", "CEREBELLAR VERMIS APLASIA", "Cerebellar vermis aplasia", "cerebellar vermis aplasia", "SPINOCEREBELLAR ATAXIA 29", "Spinocerebellar Ataxia 29", "aplasia of cerebellar vermis", "Aplasia of cerebellar vermis", "APLASIA OF CEREBELLAR VERMIS", "Spinocerebellar ataxia type 29", "spinocerebellar ataxia type 29", "SCA29 Spinocerebellar Ataxia 29", "Spinocerebellar ataxia type 29 (disorder)", "cerebellar ataxia early-onset nonprogressive", "Cerebellar ataxia, early-onset, nonprogressive", "congenital nonprogressive spinocerebellar ataxia", "Congenital nonprogressive spinocerebellar ataxia", "spinocerebellar ataxia 29, congenital nonprogressive", "cerebellar ataxia, congenital nonprogressive, autosomal dominant", "CEREBELLAR ATAXIA, CONGENITAL NONPROGRESSIVE, AUTOSOMAL DOMINANT", "Cerebellar ataxia, congenital, nonprogressive, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia type 29", "shortest_name_length": 3}
{"curie": "MONDO:0019955", "names": ["GRFoma", "GRF tumor", "Growth hormone releasing factor tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "GRFoma", "shortest_name_length": 6}
{"curie": "MONDO:0019458", "names": ["leukemia basophilic", "Basophilic leukemia", "Leukemia basophilic", "LEUKEMIA BASOPHILIC", "Leukemia Basophilic", "BASOPHILIC LEUKEMIA", "Basophilic Leukemia", "basophilic leukemia", "LEUKEMIA, BASOPHILIC", "leukemia; basophilic", "Leukaemia basophilic", "basophilic; leukemia", "Basophilic leukaemia", "Basophilic Leukemias", "[M]Basophilic leukemia", "[M]Basophilic leukaemia", "leukemia acute basophilic", "acute basophilic leukemia", "Acute Basophilic Leukemia", "Acute basophilic leukemia", "Acute Basophilic Leukemias", "Acute basophilic leukaemia", "Leukemia, Acute Basophilic", "Basophilic Leukemia, Acute", "Leukemias, Acute Basophilic", "Basophilic Leukemias, Acute", "Leukemia, Basophilic, Acute", "Basophilic leukemia (disorder)", "acute basophilic leukemia (diagnosis)", "Acute basophilic leukemia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute basophilic leukemia", "shortest_name_length": 19}
{"curie": "UMLS:C5557608", "names": ["High Grade Ureter Urothelial Carcinoma", "High-Grade Ureter Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Ureter Urothelial Carcinoma", "shortest_name_length": 38}
{"curie": "MONDO:0001491", "names": ["cough variant asthma", "Cough variant asthma", "asthma cough variant", "Cough variant asthma (disorder)", "cough variant asthma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cough variant asthma", "shortest_name_length": 20}
{"curie": "UMLS:C5420151", "names": ["Refractory Anal Canal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Anal Canal Squamous Cell Carcinoma", "shortest_name_length": 45}
{"curie": "UMLS:C1563718", "names": ["Genital Infantilism", "Infantilism, Genital"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Genital Infantilism", "shortest_name_length": 19}
{"curie": "MONDO:0013805", "names": ["MRD13", "autosomal dominant mental retardation 13", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 13", "mental retardation, autosomal dominant 13", "autosomal dominant intellectual disability 13", "intellectual disability, autosomal dominant 13", "mental retardation, autosomal dominant type 13", "intellectual disability, autosomal dominant type 13", "autosomal dominant intellectual developmental disorder 13", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 13", "autosomal dominant non-syndromic intellectual disability 13", "DYNC1H1 autosomal dominant non-syndromic intellectual disability", "mental retardation, autosomal dominant 13, with neuronal migration defects", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 13, WITH NEURONAL MIGRATION DEFECTS", "mental retardation, autosomal dominant, 13, with neuronal migration defects", "intellectual disability, autosomal dominant 13, with neuronal migration defects", "intellectual disability, autosomal dominant, 13, with neuronal migration defects", "autosomal dominant non-syndromic intellectual disability caused by mutation in DYNC1H1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 13", "shortest_name_length": 5}
{"curie": "MONDO:0024523", "names": ["BAV", "AOVD1", "bicuspid", "aortic valve disease", "AORTIC VALVE BICUSPID", "Bicuspid Aortic Valve", "aortic bicuspid valve", "Bicuspid aortic valve", "BICUSPID AORTIC VALVE", "bicuspid aortic valve", "AORTIC VALVE DISEASE 1", "Valve, Bicuspid Aortic", "AORTIC VALVE, BICUSPID", "bicuspid; aortic valve", "aortic valve disease 1", "Bicuspid Aortic Valves", "Aortic Valve Disease 1", "aortic valve, bicuspid", "Aortic Valve, Bicuspid", "aortic stenosis, calcific", "Notch1 aortic valve disease", "NOTCH1 aortic valve disease", "Bicuspid Aortic Valve Disease", "bicuspid aortic valve disorder", "aortic valve, calcification of", "[OBSOLETE] Bicuspid Aortic Valve", "Bicuspid aortic valve (disorder)", "bicuspid aortic valve (diagnosis)", "Aortic valve has two leaflets rather than three", "aortic valve disease caused by mutation in Notch1", "aortic valve disease caused by mutation in NOTCH1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic valve disease 1", "shortest_name_length": 3}
{"curie": "MONDO:0003901", "names": ["cerebellar angioblastoma", "Cerebellar Angioblastoma", "cerebellum hemangioblastoma", "cerebellar hemangioblastoma", "angioblastoma of cerebellum", "Cerebellar hemangioblastoma", "Angioblastoma of Cerebellum", "Cerebellar Hemangioblastoma", "hemangioblastoma of cerebellum", "Hemangioblastoma of Cerebellum", "angioblastoma of the cerebellum", "Angioblastoma of the Cerebellum", "Hemangioblastoma of the Cerebellum", "hemangioblastoma of the cerebellum", "Cerebellar Capillary Hemangioblastoma", "Hemangioblastoma, sporadic cerebellar", "cerebellar capillary hemangioblastoma", "cerebellar hemangioblastoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellar hemangioblastoma", "shortest_name_length": 24}
{"curie": "MONDO:0600005", "names": ["venom allergy", "venom hypersensitivity", "IgE-mediated venom hypersensitivity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "venom allergy", "shortest_name_length": 13}
{"curie": "MONDO:0003806", "names": ["HTT", "PLAT", "HTAT", "paraganglioma-like adenoma", "Paraganglioma-like Adenoma", "Hyalinizing Trabecular Tumor", "Hyalinizing trabecular tumor", "hyalinizing trabecular tumor", "Hyalinising trabecular tumour", "thyroid hyalinizing trabecular adenoma", "Thyroid Hyalinizing Trabecular Adenoma", "Hyalinizing Trabecular Adenoma of Thyroid", "hyalinizing trabecular adenoma of thyroid", "Thyroid Gland Hyalinizing Trabecular Tumor", "thyroid gland hyalinizing trabecular tumor", "hyalinizing trabecular adenoma of the thyroid", "Hyalinizing Trabecular Adenoma of the Thyroid", "Hyalinizing trabecular tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid hyalinizing trabecular adenoma", "shortest_name_length": 3}
{"curie": "UMLS:C5557178", "names": ["Stage IIIC1 Cervical Cancer AJCC v9", "Stage IIIC1 Cervical Carcinoma AJCC v9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC1 Cervical Cancer AJCC v9", "shortest_name_length": 35}
{"curie": "UMLS:C4726630", "names": ["Recurrent Head and Neck Cancer", "Recurrent Malignant Head and Neck Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Malignant Head and Neck Neoplasm", "shortest_name_length": 30}
{"curie": "MONDO:0017470", "names": ["Congenital knee dislocation", "Dislocated knee since birth", "congenital knee dislocation", "dislocation; knee, congenital", "congenital dislocation of knee", "Congenital dislocation of knee", "congenital knee dislocation (disease)", "Congenital dislocation of knee (disorder)", "congenital dislocation of knee (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital knee dislocation", "shortest_name_length": 27}
{"curie": "UMLS:C4727011", "names": ["Unresectable Carcinoid Tumor", "Unresectable Neuroendocrine Tumor G1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Neuroendocrine Tumor G1", "shortest_name_length": 28}
{"curie": "UMLS:C2828204", "names": ["Stage III Bone Cancer", "Stage III Bone Cancer AJCC v7", "Stage III Bone Cancer  AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Bone Cancer AJCC v7", "shortest_name_length": 21}
{"curie": "UMLS:C4528405", "names": ["Node-Based EBV-Positive Peripheral T-Cell Lymphoma", "Primary EBV-Positive Nodal T-Cell or NK-Cell Lymphoma", "Node-Based Epstein-Barr Virus -Positive Peripheral T-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary EBV-Positive Nodal T-Cell or NK-Cell Lymphoma", "shortest_name_length": 50}
{"curie": "UMLS:C1335579", "names": ["Pyriform Sinus Carcinoma", "Pyriform Fossa Carcinoma", "Carcinoma of pyriform fossa", "Carcinoma of Pyriform Sinus", "Carcinoma of pyriform sinus", "Carcinoma of Pyriform Fossa", "Pyriform Fossa Throat Cancer", "Carcinoma of the Pyriform Fossa", "Carcinoma of the Pyriform Sinus", "Malignant epithelial neoplasm of pyriform fossa", "Malignant epithelial neoplasm of pyriform fossa (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carcinoma of pyriform fossa", "shortest_name_length": 24}
{"curie": "MONDO:0006142", "names": ["SCCE", "Cervical Small Cell Cancer", "Cervical small cell cancer", "cervix small cell carcinoma", "carcinoma cell cervix small", "Cervix Small Cell Carcinoma", "small cell carcinoma cervix", "cervical small cell carcinoma", "Cervical Small Cell Carcinoma", "Small Cell Carcinoma of Cervix", "small cell carcinoma of cervix", "small cell cancer of the cervix", "cancer of the cervix, small cell", "cervix uteri small cell carcinoma", "Cervix Uteri Small Cell Carcinoma", "Small cell carcinoma of the cervix", "Small Cell Carcinoma of the Cervix", "small cell carcinoma of the cervix", "cervix cancer, small cell carcinoma", "uterine cervix small cell carcinoma", "carcinoma of the cervix, small cell", "Uterine Cervix Small Cell Carcinoma", "Small Cell Carcinoma of Cervix Uteri", "small cell carcinoma of cervix uteri", "cervical cancer, small cell carcinoma", "Small Cell Carcinoma of Uterine Cervix", "small cell carcinoma of uterine cervix", "Small Cell Carcinoma of the Cervix Uteri", "small cell carcinoma of the Cervix Uteri", "small cell carcinoma of the cervix uteri", "small cell carcinoma of the uterine cervix", "small cell carcinoma of cervix (diagnosis)", "Small Cell Carcinoma of the Uterine Cervix", "uterine cervix cancer, small cell carcinoma", "Cervical Small Cell Neuroendocrine Carcinoma", "uterine cervical cancer, small cell carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical small cell carcinoma", "shortest_name_length": 4}
{"curie": "UMLS:C1096266", "names": ["Streptococcus viridans group infection", "Alpha hemolytic streptococcal infection", "Alpha haemolytic streptococcal infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alpha hemolytic streptococcal infection", "shortest_name_length": 38}
{"curie": "UMLS:C4054396", "names": ["Nephrotic Syndrome - CD2AP Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - CD2AP Associated", "shortest_name_length": 37}
{"curie": "UMLS:C1334212", "names": ["Intermediate Fibrous Tumor", "Intermediate Fibrocytic Tumor", "Intermediate Fibrous Neoplasm", "Intermediate Fibrogenic Tumor", "Intermediate Fibroblastic Tumor", "Intermediate Fibrocytic Neoplasm", "Intermediate Fibrogenic Neoplasm", "Intermediate Fibroblastic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intermediate Fibroblastic Neoplasm", "shortest_name_length": 26}
{"curie": "MONDO:0007180", "names": ["De Hauwere Syndrome", "De Hauwere syndrome", "DE HAUWERE SYNDROME", "Iris Dysplasia with Ocular Hypertelorism, Psychomotor Retardation, and Sensorineural Deafness", "iris dysplasia with ocular hypertelorism, psychomotor retardation, and sensorineural deafness", "IRIS DYSPLASIA WITH OCULAR HYPERTELORISM, PSYCHOMOTOR RETARDATION, AND SENSORINEURAL DEAFNESS", "Axenfeld-Rieger Anomaly with Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, and Skeletal Abnormalities", "AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVE FACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES", "Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities", "shortest_name_length": 19}
{"curie": "MONDO:0010315", "names": ["IMD4", "IMD6", "CIDX", "XCID", "XSCID", "SCIDX", "SCIDX1", "X-SCID", "SCID-X1", "XL IL2RG", "X Linked SCID", "X-Linked SCID", "X-linked SCID", "SCID, X-LINKED", "X-Linked SCIDs", "SCID, X Linked", "SCID, X-Linked", "SCID, X-linked", "SCIDs, X-Linked", "X-linked recessive", "IMMUNODEFICIENCY 6", "IMMUNODEFICIENCY 4", "Immunodeficiency 4", "immunodeficiency 4", "Immunodeficiency 6", "gamma chain deficiency", "Thymic epithelial hypoplasia", "thymic epithelial hypoplasia", "X-Linked Immunodeficiency Disease", "X Linked Immunodeficiency Disease", "X-Linked Immunodeficiency Diseases", "X-Linked Immunodeficiency Syndrome", "Immunodeficiency Disease, X-Linked", "X Linked Immunodeficiency Syndrome", "X-Linked Combined Immunodeficiency", "X Linked Combined Immunodeficiency", "X-Linked Immunodeficiency Syndromes", "Combined Immunodeficiency, X Linked", "Immunodeficiency Diseases, X-Linked", "Immunodeficiency, X-Linked Combined", "Combined Immunodeficiency, X-Linked", "COMBINED IMMUNODEFICIENCY, X-LINKED", "Immunodeficiency Syndrome, X-Linked", "Immunodeficiency Syndromes, X-Linked", "X-Linked Combined Immunodeficiencies", "T-B+ SCID due to gamma chain deficiency", "X-linked lymphopaenic agammaglobulinemia", "X linked severe combined immunodeficiency", "X-Linked Severe Combined Immunodeficiency", "X-linked severe combined immunodeficiency", "X Linked Severe Combined Immunodeficiency", "X-linked lymphopaenic agammaglobulinaemia", "Severe Combined Immunodeficiency, X-Linked", "severe combined immunodeficiency, X-linked", "Severe Combined Immunodeficiency, X Linked", "SEVERE COMBINED IMMUNODEFICIENCY, X-LINKED", "X Linked Combined Immunodeficiency Diseases", "X-Linked Combined Immunodeficiency Diseases", "Immunodeficiency Diseases, X-Linked Combined", "Immunodeficiency Diseases, X Linked Combined", "T-B+ severe combined immunodeficiency, X-linked", "SCID - X-linked severe combined immunodeficiency", "severe combined immunodeficiency T- B+, X-linked", "XSCID - X-linked severe combined immunodeficiency", "X-linked severe combined immunodeficiency (diagnosis)", "severe combined immunodeficiency, X-linked, X-linked recessive", "T-B+ severe combined immunodeficiency due to gamma chain deficiency", "severe combined immunodeficiency T- B+ due to gamma chain deficiency", "Severe Combined Immunodeficiency, X-Linked, T Cell Negative, B Cell Positive, NK Cell Negative", "severe combined immunodeficiency, X-linked, T cell-negative, B cell-positive, NK cell-negative", "SEVERE COMBINED IMMUNODEFICIENCY, X-LINKED, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-NEGATIVE", "Severe Combined Immunodeficiency, X-Linked, T Cell-Negative, B Cell-Positive, NK Cell-Negative"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-B+ severe combined immunodeficiency due to gamma chain deficiency", "shortest_name_length": 4}
{"curie": "UMLS:C0751502", "names": ["Petrous Sinus Thromboses", "Petrous Sinus Thrombosis", "Sinus Thrombosis, Petrous", "Thrombosis, Petrous Sinus", "Sinus Thromboses, Petrous", "Thromboses, Petrous Sinus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Petrous Sinus Thrombosis", "shortest_name_length": 24}
{"curie": "UMLS:C0220644", "names": ["Pediatric HD", "Childhood HD", "pediatric HD", "childhood HD", "HD, childhood", "Hodgkin Lymphoma", "childhood Hodgkin disease", "childhood Hodgkins disease", "Childhood Hodgkin Lymphoma", "childhood Hodgkin lymphoma", "childhood Hodgkin's disease", "Pediatric Hodgkin's Disease", "Childhood Hodgkin's Disease", "childhood Hodgkins lymphoma", "pediatric Hodgkin's disease", "childhood Hodgkin's lymphoma", "Hodgkin's disease, childhood", "Childhood Hodgkin's Lymphoma", "Pediatric Hodgkin's Lymphoma", "Hodgkin's lymphoma, childhood", "lymphoma, Hodgkin's, childhood", "Lymphoma, Hodgkin lymphoma, child"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Hodgkin Lymphoma", "shortest_name_length": 12}
{"curie": "UMLS:C5205718", "names": ["Sinonasal Adenocarcinoma, Non-Salivary-Type", "Surface Epithelial (Non-Salivary-Type) Sinonasal Adenocarcinoma", "Nasal Cavity and Paranasal Sinus Adenocarcinoma, Non-Salivary-Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Adenocarcinoma, Non-Salivary-Type", "shortest_name_length": 43}
{"curie": "MONDO:0009030", "names": ["cranial nerves, recurrent paresis of", "CRANIAL NERVES, RECURRENT PARESIS OF", "Cranial Nerves, Recurrent Paresis Of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cranial nerves, recurrent paresis of", "shortest_name_length": 36}
{"curie": "MONDO:0030880", "names": ["MDPS", "mandibuloacral dysplasia progeroid syndrome", "MANDIBULOACRAL DYSPLASIA PROGEROID SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mandibuloacral dysplasia progeroid syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0019367", "names": ["Ghost Teeth", "shell teeth", "Shell teeth", "Ghost teeth", "ghost teeth", "Ghost Tooth", "Teeth, Ghost", "Tooth, Ghost", "Odontodysplasia", "odontodysplasia", "Odontodysplasias", "Odontogenic dysplasia", "Odontogenic Dysplasia", "Dysplasia, Odontogenic", "Odontogenic Dysplasias", "Shell teeth (disorder)", "shell teeth (diagnosis)", "Dysplasias, Odontogenic", "regional odontodysplasia", "Regional odontodysplasia", "odontodysplasia; regional", "Teeth with dentinal dysplasia", "Regional odontodysplasia (disorder)", "Teeth with type iii dentinogenesis imperfecta", "Teeth with thin dentin and large pulp chambers"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "regional odontodysplasia", "shortest_name_length": 11}
{"curie": "UMLS:C1336231", "names": ["Stage IIIB Small Cell Lung Cancer with Pleural Effusion", "Stage IIIB Small Cell Cancer of Lung with Pleural Effusion", "Stage IIIB Small Cell Carcinoma of Lung with Pleural Effusion", "Stage IIIB Small Cell Cancer of the Lung with Pleural Effusion", "Stage IIIB Small Cell Carcinoma of the Lung with Pleural Effusion", "Stage IIIB Lung Small Cell Carcinoma with Pleural Effusion AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Lung Small Cell Carcinoma with Pleural Effusion AJCC v7", "shortest_name_length": 55}
{"curie": "UMLS:C1168218", "names": ["Extrahepatic bile duct cancer stage I", "Extrahepatic Bile Duct Cancer Stage I", "stage I extrahepatic bile duct cancer", "Stage I Extrahepatic Bile Duct Cancer", "Stage I Extrahepatic Bile Duct Carcinoma", "Stage I Carcinoma of Extrahepatic Bile Duct", "Stage I Carcinoma of the Extrahepatic Bile Duct"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extrahepatic bile duct cancer stage I", "shortest_name_length": 37}
{"curie": "MONDO:0013378", "names": ["OFC10", "orofacial cleft 10", "Orofacial Cleft 10", "OROFACIAL CLEFT 10", "SUMO1 orofacial cleft", "orofacial cleft type 10", "orofacial cleft 10, isolated cases", "orofacial cleft caused by mutation in SUMO1", "nonsyndromic cleft lip with or without cleft palate 10", "Cleft Lip with or without Cleft Palate, Nonsyndromic, 10", "cleft lip with or without cleft palate, nonsyndromic, 10", "CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orofacial cleft 10", "shortest_name_length": 5}
{"curie": "MONDO:0003110", "names": ["skin angioma", "Skin Angioma", "angioma of skin", "Angioma of Skin", "Angioma of skin", "hemangioma skin", "Skin Hemangioma", "skin hemangioma", "Haemangioma;skin", "Hemangioma of skin", "hemangioma of skin", "Hemangioma of Skin", "Angioma of the skin", "Haemangioma of skin", "angioma of the skin", "Angioma of the Skin", "skin tumor vascular", "skin tumors vascular", "cutaneous hemangioma", "HEMANGIOMA CUTANEOUS", "cutaneous hemangiomas", "Hemangioma of the Skin", "hemangioma of the skin", "zone of skin hemangioma", "haemangioma of the skin", "Angiomatous nevus of skin", "Angiomatous naevus of skin", "angiomatous naevus of skin", "hemangioma of zone of skin", "Hemangioma of skin (disorder)", "hemangioma of skin (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin hemangioma", "shortest_name_length": 12}
{"curie": "MONDO:0019969", "names": ["panner disease", "Osteochondrosis of the capital humerus", "aseptic necrosis of the capital humerus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "panner disease", "shortest_name_length": 14}
{"curie": "UMLS:C0341503", "names": ["Septic peritonitis", "septic; peritonitis", "peritonitis; septic", "Bacterial Peritonitis", "Bacterial peritonitis", "Peritonitis bacterial", "bacterial peritonitis", "PERITONITIS BACTERIAL", "Peritonitis bacterial NOS", "Bacterial peritonitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bacterial peritonitis", "shortest_name_length": 18}
{"curie": "MONDO:0009275", "names": ["Nh", "NH", "Nhc", "NHC", "neonatal Hepatitis", "giant cell Hepatitis", "hemochromatosis neonatal", "Neonatal Hemochromatosis", "Neonatal hemochromatosis", "neonatal hemochromatosis", "HEMOCHROMATOSIS, NEONATAL", "neonatal haemochromatosis", "Hemochromatosis, Neonatal", "Neonatal haemochromatosis", "hemochromatosis, neonatal", "NEONATAL HEPATITIS, FORMERLY", "neonatal Hepatitis, formerly", "neonatal giant cell hepatitis", "Neonatal giant cell hepatitis", "neonatal hepatitis (formerly)", "giant cell Hepatitis, formerly", "GIANT CELL HEPATITIS, FORMERLY", "giant cell Hepatitis (formerly)", "alloimmune Hepatitis, congenital", "ALLOIMMUNE HEPATITIS, CONGENITAL", "Idiopathic neonatal hemochromatosis", "Idiopathic Neonatal Hemochromatosis", "idiopathic neonatal hemochromatosis", "Neonatal hemochromatosis (disorder)", "Idiopathic neonatal haemochromatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal hemochromatosis", "shortest_name_length": 2}
{"curie": "MONDO:0006248", "names": ["HYDM", "Hydatid Mole", "hydatid mole", "Hydatid mole", "Hydatid Moles", "Mole, Hydatid", "MOLE, HYDATID", "Vesicular mole", "mole pregnancy", "vesicular mole", "Moles, Hydatid", "pregnancy mole", "MOLAR PREGNANCY", "vesicular; mole", "Molar pregnancy", "Molar Pregnancy", "moles pregnancy", "mole; vesicular", "chorionic tumor", "molar pregnancy", "pregnancy; mole", "PREGNANCY, MOLAR", "Pregnancy, Molar", "molars pregnancy", "HYDATIDIFORM MOLE", "hydatidiform mole", "molar pregnancies", "mole hydatidiform", "Hydatidiform Mole", "Hydatidiform mole", "Molar Pregnancies", "hydatidiform moles", "Mole, Hydatidiform", "Pregnancies, Molar", "MOLE, HYDATIDIFORM", "mole; hydatidiform", "hydatidiform; mole", "Hydatidiform Moles", "Moles, Hydatidiform", "Molar pregnancy, NOS", "hydatidiform mole GTT", "Hydatidiform mole NOS", "Hydatidiform mole, NOS", "GTT, hydatidiform mole", "Mole of pregnancy, NOS", "Hydatidiform mole benign", "HYDATIDIFORM MOLE BENIGN", "Benign hydatidiform mole", "Hydatidiform mole, benign", "molar pregnancy; pregnancy", "Classical hydatidiform mole", "pregnancy; hydatidiform mole", "hydatidiform mole; classical", "hydatidiform mole, recurrent", "classical; hydatidiform mole", "mole; hydatidiform, classical", "pregnancy; mole, hydatidiform", "hydatidiform mole (diagnosis)", "mole; pregnancy, hydatidiform", "Hydatidiform mole, unspecified", "Molar pregnancy with hydatid mole", "Molar pregnancy with vesicular mole", "molar pregnancy (non-metastatic GTD)", "Hydatidiform mole, benign (disorder)", "Hydatidiform mole, benign (diagnosis)", "Molar pregnancy with hydatidiform mole", "gestational trophoblastic tumor, hydatidiform mole", "Hydatidiform mole, benign (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hydatidiform mole", "shortest_name_length": 4}
{"curie": "MONDO:0020304", "names": ["Isochromosomy Yp", "isochromosomy Yp", "Isochromosome Yp", "Isochromosomy Yp (disorder)", "Isochromosomy Yp (diagnosis)", "anomaly of chromosome y isochromosomy yp"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isochromosomy Yp", "shortest_name_length": 16}
{"curie": "MONDO:0008812", "names": ["AREDYLD", "AREDYLD Syndrome", "AREDYLD syndrome", "Acral renal ectodermal dysplasia lipoatrophic diabetes", "acral renal ectodermal dysplasia lipoatrophic diabetes", "acrorenal defect-ectodermal dysplasia-diabetes syndrome", "Acrorenal defect-ectodermal dysplasia-diabetes syndrome", "Acrorenal field defect, ectodermal dysplasia, and lipoatrophic diabetes", "ACRORENAL FIELD DEFECT, ECTODERMAL DYSPLASIA, AND LIPOATROPHIC DIABETES", "acrorenal Field defect, ectodermal dysplasia, and lipoatrophic diabetes", "Acrorenal field defect, ectodermal dysplasia, and lipoatrophic diabetes (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AREDYLD syndrome", "shortest_name_length": 7}
{"curie": "UMLS:C1378461", "names": ["Stage IV Esophageal Cancer", "Stage IV Esophagus Carcinoma", "stage IV cancer of the esophagus", "Stage IV Esophageal Cancer AJCC v6", "Stage IV Esophagus Carcinoma AJCC v6", "Stage IV Esophageal Carcinoma AJCC v6", "Stage IV Carcinoma of Esophagus AJCC v6", "Stage IV Carcinoma of the Esophagus AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Esophagus Carcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0009688", "names": ["MG", "Erb-Goldflam", "Goldflam-Erb", "myasthenia gravis", "MYASTHENIA GRAVIS", "Myasthenia Gravis", "Myasthenia gravis", "gravis; myasthenia", "myasthenia; gravis", "Acquired myasthenia", "acquired myasthenia", "Erb-Goldflam disease", "Erb-Goldflam syndrome", "Myasthenia gravis NOS", "Myasthenia gravis, NOS", "myasthenia gravis (MG)", "MG - Myasthenia gravis", "myasthenia gravis disorder", "Myasthenia gravis paralytica", "Myasthenia gravis (disorder)", "Autoimmune myasthenia gravis", "autoimmune myasthenia gravis", "myasthenia gravis (diagnosis)", "myasthenia gravis without acute exacerbation", "Myasthenia gravis without (acute) exacerbation", "myasthenia gravis without acute exacerbation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myasthenia gravis", "shortest_name_length": 2}
{"curie": "MONDO:0003032", "names": ["superior vena cava angiosarcoma", "Superior Vena Cava Angiosarcoma", "Angiosarcoma of Superior Vena Cava", "angiosarcoma of Superior vena cava", "Angiosarcoma of the Superior Vena Cava", "angiosarcoma of the Superior Vena Cava", "angiosarcoma of the Superior vena cava", "anterior vena cava angiosarcoma (disease)", "angiosarcoma (disease) of anterior vena cava"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "superior vena cava angiosarcoma", "shortest_name_length": 31}
{"curie": "UMLS:C4721648", "names": ["Stage I Esophageal Squamous Cell Cancer", "Stage I Esophagus Squamous Cell Carcinoma", "Stage I Esophageal Squamous Cell Carcinoma", "Esophageal Squamous Cell Carcinoma Stage I", "Oesophageal Squamous Cell Carcinoma Stage I", "Stage I Squamous Cell Carcinoma of Esophagus", "Stage I Squamous Cell Carcinoma of the Esophagus", "Stage I Esophageal Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Esophageal Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 39}
{"curie": "MONDO:0008754", "names": ["ACD-mental retardation syndrome", "ACD MENTAL RETARDATION SYNDROME", "ACD Mental Retardation Syndrome", "ACD mental retardation syndrome", "ACD intellectual disability syndrome", "ACD-intellectual disability syndrome", "Alopecia contractures dwarfism mental retardation", "alopecia-contractures-dwarfism-mental retardation syndrome", "ALOPECIA-CONTRACTURES-DWARFISM MENTAL RETARDATION SYNDROME", "Alopecia-contractures-dwarfism mental retardation syndrome", "alopecia-contractures-dwarfism mental retardation syndrome", "alopecia-contractures-dwarfism intellectual disability syndrome", "alopecia - contractures - dwarfism - intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alopecia - contractures - dwarfism - intellectual disability syndrome", "shortest_name_length": 31}
{"curie": "UMLS:C4288379", "names": ["Cervical Postoperative Spindle Cell Nodule", "Postoperative Spindle Cell Nodule of the Cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postoperative Spindle Cell Nodule of the Cervix", "shortest_name_length": 42}
{"curie": "MONDO:0004038", "names": ["Enamel dysplasia", "Thin tooth enamel", "Hypoplasia enamel", "HYPOPLASIA ENAMEL", "Enamel Hypoplasia", "ENAMEL HYPOPLASIA", "Enamel hypoplasia", "Enamel hypotrophy", "enamel hypoplasia", "Thin dental enamel", "Enamel Hypoplasias", "Hypoplasia, Enamel", "Hypoplastic enamel", "Hypoplastic Enamel", "Enamel, Hypoplastic", "Enamel, underdeveloped", "Defective enamel matrix", "teeth enamel hypoplasia", "TOOTH ENAMEL HYPOPLASIA", "tooth enamel hypoplasia", "dental enamel hypoplasia", "Dental Enamel Hypoplasia", "Dental enamel hypoplasia", "Enamel Hypoplasia, Dental", "Hypoplasia, Dental Enamel", "Dysplasia of tooth enamel", "Hypoplasia of tooth enamel", "Hypoplasia of dental enamel", "Enamel dysplasia (disorder)", "hypoplasia; enamel of teeth", "Underdeveloped teeth enamel", "enamel of teeth; hypoplasia", "Enamel hypoplasia (disorder)", "tooth enamel hypoplasia (diagnosis)", "teeth enamel hypoplasia (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dental enamel hypoplasia", "shortest_name_length": 16}
{"curie": "UMLS:C5237755", "names": ["Recurrent Large Pleural Effusion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Large Pleural Effusion", "shortest_name_length": 32}
{"curie": "MONDO:0024263", "names": ["Fetal aspiration syndrome", "fetal aspiration syndrome", "Neonatal Aspiration Syndrome", "neonatal aspiration syndrome", "Neonatal aspiration syndrome", "Neonatal aspiration syndromes", "syndrome; aspiration, newborn", "aspiration; syndrome of newborn", "Aspiration syndrome in the newborn", "Neonatal aspiration syndrome (disorder)", "Neonatal aspiration syndrome, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal aspiration syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0012485", "names": ["DFNB68", "autosomal recessive deafness 68", "DEAFNESS, AUTOSOMAL RECESSIVE 68", "deafness, autosomal recessive 68", "Deafness, Autosomal Recessive 68", "autosomal recessive nonsyndromic deafness 68", "S1PR2 autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 68", "autosomal recessive nonsyndromic deafness type 68", "autosomal recessive nonsyndromic deafness caused by mutation in S1PR2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 68", "shortest_name_length": 6}
{"curie": "UMLS:C4727010", "names": ["Unresectable Pancreatic Neuroendocrine Cancer", "Unresectable Pancreatic Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Pancreatic Neuroendocrine Carcinoma", "shortest_name_length": 45}
{"curie": "MONDO:0005564", "names": ["EMBT", "embryo cancer", "embryo neoplasm", "embryonal tumor", "Embryonal tumors", "embryonal cancer", "Embryonal tumours", "Tumors, Embryonal", "embryonal neoplasm", "Embryonal neoplasm", "Embryonal Neoplasm", "Embryonal Neoplasms", "Embryonal neoplasia", "Neoplasm, Embryonal", "Neoplasms, Embryonal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "embryonal neoplasm", "shortest_name_length": 4}
{"curie": "MONDO:0017219", "names": ["SMMCI", "HPE-L", "Microform HPE", "fused incisors", "HPE, minor form", "holoprosencephaly-like", "microform holoprosencephaly", "single upper central incisor", "Holoprosencéphalie, minor form", "HoloprosencC)phalie, minor form", "single central maxillary incisor", "single median maxillary central incisor", "solitary median maxillary central incisor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microform holoprosencephaly", "shortest_name_length": 5}
{"curie": "MONDO:0007964", "names": ["CMM2", "Clark Nevus", "atypical nevi", "Atypical mole", "Clark's Nevus", "FAMM syndrome", "atypical nevis", "atypical nevus", "Atypical nevus", "Atypical Nevus", "Atypical naevus", "Dysplastic nevi", "dysplastic nevi", "Dysplastic Nevi", "atypical naevus", "dysplastic nevus", "Dysplastic nevus", "Dysplastic Nevus", "Nevi, Dysplastic", "dysplastic nevis", "Dysplastic naevus", "Lentiginous Nevus", "B-K MOLE SYNDROME", "B K Mole Syndrome", "Lentiginous nevus", "naevus dysplastic", "B-K Mole syndrome", "dysplastic naevus", "Nevus, Dysplastic", "B-K Mole Syndrome", "B-K mole syndrome", "Syndrome, B-K Mole", "Lentiginous naevus", "[M] Dysplastic nevus", "DN - Dysplastic nevus", "[M] Dysplastic naevus", "Atypical nevus of skin", "Atypical mole syndrome", "atypical mole syndrome", "Atypical Mole syndrome", "Atypical Mole Syndrome", "DN - Dysplastic naevus", "Atypical naevus of skin", "Dysplastic nevus of skin", "familial dysplastic nevi", "Familial Dysplastic Nevi", "B-K mole (nevus) syndrome", "dysplastic nevus syndrome", "Dysplastic naevus of skin", "Dysplastic Nevus Syndrome", "Dysplastic nevus syndrome", "Nevus Syndrome, Dysplastic", "Dysplastic naevus syndrome", "B-K mole (naevus) syndrome", "dysplastic naevus syndrome", "Syndrome, Dysplastic Nevus", "dysplastic nevus (diagnosis)", "melanoma, cutaneous malignant, 2", "Nevus with Architectural Disorder", "Atypical mole syndrome (disorder)", "Dysplastic nevus of skin (disorder)", "Familial Atypical Multiple Mole-Melanoma", "familial atypical multiple mole-melanoma", "Familial Atypical Multiple Mole Melanoma", "Dysplastic nevus (morphologic abnormality)", "susceptibility to cutaneous malignant melanoma 2", "Familial atypical mole malignant melanoma syndrome", "MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2", "melanoma, cutaneous malignant, susceptibility to, 2", "melanoma, cutaneous malignant, susceptibility to, type 2", "FAMMM - Familial atypical mole malignant melanoma syndrome", "Nevus with Architectural Disorder and Cytologic Atypia of Melanocytes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melanoma, cutaneous malignant, susceptibility to, 2", "shortest_name_length": 4}
{"curie": "MONDO:0022330", "names": ["4-hydroxyphenylacetic aciduria", "Elevated urine 4-hydroxyphenylacetic acid level"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "4-hydroxyphenylacetic aciduria", "shortest_name_length": 30}
{"curie": "UMLS:C1336300", "names": ["Stage II Nasal Cavity Cancer", "Stage II Nasal Cavity Carcinoma", "Stage II Carcinoma of Nasal Cavity", "Stage II Carcinoma of the Nasal Cavity", "Stage II Nasal Cavity Carcinoma AJCC v6", "Stage II Nasal Cavity Carcinoma AJCC v7", "Stage II Nasal Cavity Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Nasal Cavity Cancer AJCC v6 and v7", "shortest_name_length": 28}
{"curie": "MONDO:0007358", "names": ["familial dyskeratotic comedone", "Familial dyskeratotic comedones", "COMEDONES, FAMILIAL DYSKERATOTIC", "comedones, familial Dyskeratotic", "Comedones, Familial Dyskeratotic", "acne comedone familial dyskeratotic", "familial dyskeratotic comedone (diagnosis)", "Familial dyskeratotic comedones (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "comedones, familial Dyskeratotic", "shortest_name_length": 30}
{"curie": "MONDO:0014769", "names": ["OOMD", "oocyte maturation defect", "inherited oocyte maturation defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited oocyte maturation defect", "shortest_name_length": 4}
{"curie": "MONDO:0010641", "names": ["DL-ATS", "ATS-DL", "Xq22.3 microdeletion syndrome", "diffuse leiomyomatosis in Alport syndrome", "Diffuse leiomyomatosis in Alport syndrome", "Alport syndrome and diffuse leiomyomatosis", "Alport Syndrome And Diffuse Leiomyomatosis", "ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS", "Alport syndrome with diffuse leiomyomatosis", "Diffuse Leiomyomatosis With Alport Syndrome", "leiomyomatosis, diffuse, with Alport syndrome", "LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME", "chromosome Xq22.3 centromeric deletion syndrome", "CHROMOSOME Xq22.3 CENTROMERIC DELETION SYNDROME", "X-linked diffuse leiomyomatosis-Alport syndrome", "LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY", "Leiomyomatosis, esophageal and vulval, with nephropathy", "leiomyomatosis, esophageal and vulval, with nephropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked diffuse leiomyomatosis-Alport syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C0751716", "names": ["Adult Neuroaxonal Dystrophy", "Neuroaxonal Dystrophy, Adult", "Dystrophy, Adult Neuroaxonal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Neuroaxonal Dystrophy", "shortest_name_length": 27}
{"curie": "MONDO:0017914", "names": ["pure or complex autosomal dominant spastic paraplegia", "Pure or complicated autosomal dominant spastic paraplegia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pure or complex autosomal dominant spastic paraplegia", "shortest_name_length": 53}
{"curie": "UMLS:C1882414", "names": ["Polyarticular JRA", "Polyarticular Still Disease", "Polyarticular Still's Disease", "Polyarticular Juvenile Rheumatoid Arthritis (AQ)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Polyarticular Still Disease", "shortest_name_length": 17}
{"curie": "UMLS:C4521637", "names": ["Stage 0 Esophageal Adenocarcinoma", "Clinical Stage 0 Esophageal Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage 0 Esophageal Adenocarcinoma AJCC v8", "shortest_name_length": 33}
{"curie": "MONDO:0004372", "names": ["chronic toxic polyneuropathy", "Chronic Toxic Polyneuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic toxic polyneuropathy", "shortest_name_length": 28}
{"curie": "MONDO:0018698", "names": ["hereditary neuroendocrine tumor of small bowel", "hereditary neuroendocrine tumor of small intestine", "hereditary small intestine neuroendocrine neoplasm", "hereditary neuroendocrine tumor of the small intestine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary neuroendocrine tumor of small intestine", "shortest_name_length": 46}
{"curie": "MONDO:0009038", "names": ["Lowry syndrome", "Craniosynostosis with Fibular Aplasia", "CRANIOSYNOSTOSIS WITH FIBULAR APLASIA", "craniosynostosis with fibular aplasia", "Craniosynostosis fibular aplasia syndrome", "craniosynostosis-fibular aplasia syndrome", "Craniosynostosis fibular aplasia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniosynostosis-fibular aplasia syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0006273", "names": ["hyalinizing spindle cell tumor with giant Rosettes", "Hyalinizing Spindle Cell Tumor with Giant Rosettes", "low grade fibromyxoid sarcoma with giant collagen rosettes", "Low Grade Fibromyxoid Sarcoma with Giant Collagen Rosettes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "low grade fibromyxoid sarcoma with giant collagen rosettes", "shortest_name_length": 50}
{"curie": "MONDO:0024310", "names": ["GASTRIC ANGIODYSPLASIA", "gastric angiodysplasia", "Gastric angiodysplasia", "stomach angiodysplasia", "Angiodysplasia of stomach", "angiodysplasia of stomach", "Gastric vascular dysplasia", "gastric vascular dysplasia", "Angiodysplasia of stomach (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angiodysplasia of stomach", "shortest_name_length": 22}
{"curie": "UMLS:C4725806", "names": ["Refractory Malignant Oral Neoplasm", "Refractory Malignant Lip and Oral Cavity Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Malignant Oral Neoplasm", "shortest_name_length": 34}
{"curie": "UMLS:C5420073", "names": ["Peritoneal Implant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peritoneal Implant", "shortest_name_length": 18}
{"curie": "MONDO:0008517", "names": ["Spel syndrome", "SPEL SYNDROME", "syndactyly-polydactyly-earlobe syndrome", "SYNDACTYLY-POLYDACTYLY-EARLOBE SYNDROME", "Syndactyly-Polydactyly-Earlobe Syndrome", "syndactyly-polydactyly-ear lobe syndrome", "hallux syndactyly ulnar polydactyly abnormal ear lobes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndactyly-polydactyly-ear lobe syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0011538", "names": ["Frontoocular Syndrome", "FRONTOOCULAR SYNDROME", "frontoocular syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontoocular syndrome", "shortest_name_length": 21}
{"curie": "MONDO:0018583", "names": ["human infection by orthopoxvirus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "human infection by orthopoxvirus", "shortest_name_length": 32}
{"curie": "MONDO:0001991", "names": ["malignant heart germ cell tumor", "Malignant Heart Germ Cell Tumor", "Malignant Cardiac Germ Cell Tumor", "malignant Cardiac germ cell tumor", "malignant cardiac germ cell tumor", "malignant heart germ cell neoplasm", "Malignant Germ Cell Tumor of Heart", "malignant germ cell tumor of heart", "Malignant Heart Germ Cell Neoplasm", "malignant cardiac germ cell tumour", "Malignant Cardiac Germ Cell Neoplasm", "malignant Cardiac germ cell neoplasm", "malignant germ cell neoplasm of heart", "Malignant Germ Cell Neoplasm of Heart", "Malignant germ cell neoplasm of heart", "malignant germ cell tumor of the heart", "Malignant Germ Cell Tumor of the Heart", "malignant germ cell tumor of the Heart", "malignant germ cell tumour of the Heart", "Malignant Germ Cell Neoplasm of the Heart", "malignant germ cell neoplasm of the heart", "malignant cardiac neoplasm of heart germ cell", "Malignant germ cell neoplasm of heart (disorder)", "Malignant germ cell neoplasm of heart (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant cardiac germ cell tumor", "shortest_name_length": 31}
{"curie": "MONDO:0042969", "names": ["trisomy 12q", "Trisomy 12q", "12q trisomy", "12q+ syndrome", "Duplication 12q", "12q duplication", "dup(12q) syndrome", "partial trisomy 12q", "chromosome 12q trisomy", "duplication 12q syndrome", "12q duplication syndrome", "Chromosome 12, trisomy 12q", "chromosome 12q duplication", "chromosome 12q duplication syndrome", "partial duplication of the long arm of chromosome 12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of the long arm of chromosome 12", "shortest_name_length": 11}
{"curie": "UMLS:C1332842", "names": ["Salivary Gland Carcinosarcoma", "Carcinosarcoma of Salivary Gland", "carcinosarcoma of salivary gland", "Carcinosarcoma of the Salivary Gland", "carcinosarcoma of salivary gland (diagnosis)", "True Malignant Mixed Tumor of the Salivary Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinosarcoma of salivary gland", "shortest_name_length": 29}
{"curie": "MONDO:0001712", "names": ["Alexia", "alexia", "ALEXIA", "Alexias", "alexias", "Alexia, NOS", "Aphemesthesia", "Aphemesthaesia", "Word blindness", "Optical alexia", "Text blindness", "Visual amnesia", "aphemesthaesia", "acquired alexia", "Alexia (finding)", "alexia, acquired", "acquired dyslexia", "Acquired Dyslexia", "Dyslexia, Acquired", "alexia (diagnosis)", "Acquired Word Blindness", "acquired Word blindness", "blindness, acquired Word", "Word Blindness, Acquired", "acquired global dyslexia", "Word blindness, acquired", "Blindness, Acquired Word", "Acquired Word Blindnesses", "acquired Word Blindnesses", "global dyslexia, acquired", "dyslexia, acquired global", "acquired spelling dyslexia", "Word Blindnesses, acquired", "Blindnesses, Acquired Word", "Word Blindnesses, Acquired", "Blindnesses, acquired Word", "acquired reading disability", "Acquired Reading Disability", "spelling dyslexia, acquired", "dyslexia, acquired spelling", "disability, acquired reading", "Disability, Acquired Reading", "reading disability, acquired", "Reading Disability, Acquired", "Acquired Reading Disabilities", "acquired reading disabilities", "disabilities, acquired reading", "reading disabilities, acquired", "Disabilities, Acquired Reading", "Reading Disabilities, Acquired"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alexia", "shortest_name_length": 6}
{"curie": "MONDO:0021077", "names": ["Cystic Tumor", "cystic tumor", "Cystic Neoplasm", "cystic neoplasm", "Neoplasm, Cystic", "Cystic Neoplasms", "Neoplasms, Cystic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cystic neoplasm", "shortest_name_length": 12}
{"curie": "MONDO:0018361", "names": ["neonatal scleroderma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal scleroderma", "shortest_name_length": 20}
{"curie": "MONDO:0017749", "names": ["disorder of multiple glycosylation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of multiple glycosylation", "shortest_name_length": 34}
{"curie": "MONDO:0006042", "names": ["TBM", "meningeal TB", "TB Meningitis", "tb meningitis", "TB meningitis", "meningitis tb", "TB Meningitides", "tubercular meningitis", "tuberculosis meninges", "Tubercular meningitis", "Tubercular Meningitis", "Tuberculosis;meninges", "Meningitis tuberculous", "TUBERCULOUS MENINGITIS", "Tuberculous Meningitis", "Meningeal Tuberculoses", "tuberculous meningitis", "meningitis tuberculous", "Meningeal tuberculosis", "Meninges--Tuberculosis", "meningeal tuberculosis", "Meningitis, Tubercular", "MENINGITIS TUBERCULOUS", "Meningeal Tuberculosis", "Tuberculous meningitis", "tuberculosis meningeal", "Meningitis, Tuberculous", "Tubercular Meningitides", "tuberculosis meningitis", "Tuberculosis, Meningeal", "Tuberculosis Meningitis", "meningitis tuberculosis", "Tuberculoses, Meningeal", "MENINGITIS, TUBERCULOUS", "Tuberculosis of meninges", "Meningitis, Tuberculosis", "Meningitides, Tubercular", "Tuberculous Meningitides", "Tuberculosis Meningitides", "Meningitides, Tuberculous", "Meningitides, Tuberculosis", "TB - Tuberculous meningitis", "TBM - Tuberculous meningitis", "tubercular meningitis (diagnosis)", "Tuberculous meningitis, unspecified", "Tuberculosis of meninges (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "meningeal tuberculosis", "shortest_name_length": 3}
{"curie": "MONDO:0008910", "names": ["Kininase I deficiency", "Deficiency of protaminase", "CARBOXYPEPTIDASE N DEFICIENCY", "carboxypeptidase N deficiency", "Carboxypeptidase N deficiency", "Carboxypeptidase B deficiency", "Carboxypeptidase N Deficiency", "deficiency of carboxypeptidase B", "Deficiency of carboxypeptidase B", "anaphylatoxin inactivator deficiency", "anaphylotoxin inactivator deficiency", "Anaphylotoxin inactivator deficiency", "Deficiency of carboxypeptidase B (disorder)", "Anaphylotoxin inactivator deficiency (disorder)", "anaphylatoxin inactivator deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carboxypeptidase N deficiency", "shortest_name_length": 21}
{"curie": "UMLS:C1567426", "names": ["Unilateral MCDK", "Unilateral multicystic renal dysplasia", "Unilateral multicystic dysplastic kidney", "Unilateral Multicystic Dysplastic Kidney", "Multicystic dysplastic kidney, unilateral", "Unilateral MCKD (multicystic kidney disease)", "Unilateral multicystic renal dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unilateral Multicystic Dysplastic Kidney", "shortest_name_length": 15}
{"curie": "MONDO:0019277", "names": ["epidermal appendage anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermal appendage anomaly", "shortest_name_length": 27}
{"curie": "UMLS:C5446562", "names": ["Lacrimal Gland Mucosa-Associated Lymphoid Tissue Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lacrimal Gland Mucosa-Associated Lymphoid Tissue Lymphoma", "shortest_name_length": 57}
{"curie": "UMLS:C4721661", "names": ["Stage IV Squamous Cell Lung Cancer", "Stage IV Squamous Cell Lung Carcinoma", "Stage IV Epidermoid Cell Lung Carcinoma", "Stage IV Squamous Cell Carcinoma of Lung", "Stage IV Epidermoid Cell Carcinoma of Lung", "Stage IV Squamous Cell Carcinoma of the Lung", "Stage IV Lung Squamous Cell Carcinoma AJCC v7", "Stage IV Squamous Cell Lung Carcinoma AJCC v7", "Stage IV Epidermoid Cell Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Lung Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 34}
{"curie": "UMLS:C1336332", "names": ["Stage IVA Bladder Cancer", "Stage IVA Urinary Bladder Cancer", "Stage IVA Urinary Bladder Carcinoma", "Jewett-Marshall Stage D1 Bladder Cancer", "Jewett-Marshall Stage D1 Urinary Bladder Cancer", "Jewett-Marshall Stage D1 Urinary Bladder Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Bladder Cancer", "shortest_name_length": 24}
{"curie": "MONDO:0032712", "names": ["COXPD38", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 38", "combined oxidative phosphorylation deficiency 38"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation deficiency 38", "shortest_name_length": 7}
{"curie": "MONDO:0017457", "names": ["bifid hallux", "bifid halluces", "Accessory hallux", "bifid great toes", "hallux; accessory", "accessory; hallux", "Preaxial polydactyly of toe", "preaxial polydactyly of foot", "Preaxial polydactyly of toes", "Preaxial polydactyly of toe (disorder)", "Preaxial polydactyly of toe (diagnosis)", "congenital deformity toes polydactyly preaxial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Preaxial polydactyly of toes", "shortest_name_length": 12}
{"curie": "MONDO:0011656", "names": ["PDB4", "Paget disease of bone-4", "paget disease of bone 4", "Paget disease of bone 4", "Paget Disease Of Bone 4", "PAGET DISEASE OF BONE 4", "Paget's disease of bone 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paget disease of bone 4", "shortest_name_length": 4}
{"curie": "OMIM:615602", "names": ["MEMRYQTL", "MEMORY QUANTITATIVE TRAIT LOCUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 8}
{"curie": "MONDO:0004225", "names": ["BMH", "MGUS", "mgus", "MGUS undetermined", "gammopathy monoclonal", "monoclonal gammopathy", "GAMMOPATHY MONOCLONAL BENIGN", "Benign Monoclonal Gammopathy", "Benign monoclonal gammopathy", "benign monoclonal gammopathy", "benign monoclonal gammapathy", "Benign Monoclonal Gammapathy", "BENIGN MONOCLONAL GAMMOPATHY", "Monoclonal Gammapathy, Benign", "Monoclonal Gammopathy, Benign", "monoclonal gammopathy, benign", "Benign Monoclonal Gammopathies", "Benign Monoclonal Gammapathies", "Monoclonal Gammapathies, Benign", "Monoclonal Gammopathies, Benign", "Asymptomatic monoclonal gammopathy", "Benign monoclonal gammopathy (disorder)", "benign monoclonal hypergammaglobulinemia", "BENIGN MONOCLONAL HYPERGAMMAGLOBUMINEMIA", "Hypergammaglobulinemia benign monoclonal", "Benign monoclonal hypergammaglobulinemia", "Benign monoclonal hypergammaglobulinaemia", "Hypergammaglobulinaemia benign monoclonal", "GAMMOPATHY MONOCLONAL UNCERTAIN SIGNIFICANCE", "Monoclonal Gammopathy of Unknown Significance", "Monoclonal gammopathy of unknown significance", "monoclonal gammopathy of unknown significance", "Monoclonal gammopathy of uncertain significance", "monoclonal gammopathy of uncertain significance", "Monoclonal Gammopathy of Undetermined Significance", "monoclonal gammopathy of undetermined significance", "Monoclonal Gammapathy of Undetermined Significance", "Monoclonal gammopathy of undetermined significance", "gammopathy; monoclonal, of undetermined significance", "benign monoclonal hypergammaglobulinemia (diagnosis)", "monoclonal; gammopathy, of undetermined significance", "MGUS - Monoclonal gammopathy of uncertain significance", "monoclonal gammopathy Of undetermined significance (MGUS)", "Monoclonal Gammopathy of Undetermined Significance (MGUS)", "Monoclonal gammopathy of undetermined significance [MGUS]", "monoclonal gammopathy of undetermined significance (MGUS)", "Monoclonal gammopathy of undetermined significance (MGUS)", "Monoclonal gammopathy of uncertain significance (disorder)", "monoclonal gammopathy of undetermined significance (diagnosis)", "plasma cell neoplasm, monoclonal gammopathy of unknown significance", "monoclonal gammopathy of undetermined significance (morphologic abnormality)", "Monoclonal gammopathy of undetermined significance (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "monoclonal gammopathy of uncertain significance", "shortest_name_length": 3}
{"curie": "UMLS:C4522237", "names": ["Recurrent Soft Tissue Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Soft Tissue Sarcoma", "shortest_name_length": 29}
{"curie": "MONDO:0016309", "names": ["Niemann-Pick disease type C, classic form", "Niemann-Pick disease type C, juvenile neurologic onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Niemann-Pick disease type C, juvenile neurologic onset", "shortest_name_length": 41}
{"curie": "UMLS:C4683012", "names": ["Stage IA Eyelid Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Eyelid Carcinoma AJCC v8", "shortest_name_length": 33}
{"curie": "MONDO:0007655", "names": ["Grooved tongue", "tongue scrotal", "Lingue plicata", "Lingua Plicata", "LINGUA PLICATA", "Cracked tongue", "tongue fissure", "lingua plicata", "Lingual furrow", "Lingua plicata", "SCROTAL TONGUE", "Scrotal tongue", "fissure tongue", "TONGUE FISSURE", "scrotal tongue", "Scrotal Tongue", "Scrotal Tongues", "Fissured tongue", "lingua; plicata", "Furrowed Tongue", "tongue; fissure", "fissure; tongue", "fissures tongue", "furrowed tongue", "tongue; scrotal", "Fissured Tongue", "Tongue, Scrotal", "plicated tongue", "Lingua Plicatas", "scrotum; tongue", "plicata; lingua", "Furrowed tongue", "fissured tongue", "Plicata, Lingua", "Plicated tongue", "tongue fissured", "furrowed; tongue", "tongue; furrowed", "Tongue, Furrowed", "Fissured Tongues", "tongue, fissured", "fissuring tongue", "Tongue, Fissured", "erythema migrans", "Furrowed Tongues", "Tongues, Scrotal", "Plicatas, Lingua", "fissure of tongue", "Tongues, Furrowed", "Fissure of tongue", "Tongues, Fissured", "Prominent tongue grooves", "ectopic geographic tongue", "congenital plicated tongue", "Plicated tongue (disorder)", "Congenital plicated tongue", "glossitis, benign migratory", "plicated tongue (diagnosis)", "Congenital fissure of tongue", "congenital fissure of tongue", "fissure of tongue, congenital", "Fissure of tongue, congenital", "GEOGRAPHIC AND FISSURED TONGUE", "geographic and fissured tongue", "scrotal tongue (physical finding)", "geographic tongue and fissured tongue", "Geographic Tongue and Fissured Tongue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fissured tongue", "shortest_name_length": 14}
{"curie": "UMLS:C1282509", "names": ["metastasis from malignant neoplasm of thyroid", "metastasis from malignant neoplasm of thyroid (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metastasis from malignant neoplasm of thyroid", "shortest_name_length": 45}
{"curie": "UMLS:C1541260", "names": ["Stage II Indolent Non-Hodgkin Lymphoma", "Stage II Indolent Adult Non-Hodgkin Lymphoma", "stage II indolent adult non-Hodgkin lymphoma", "indolent, stage II adult non-Hodgkin lymphoma", "Ann Arbor Stage II Indolent Adult Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Indolent Adult Non-Hodgkin Lymphoma", "shortest_name_length": 38}
{"curie": "UMLS:C3897531", "names": ["Stage IIIA Rectal Cancer", "Stage IIIA Rectal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Rectal Cancer AJCC v7", "shortest_name_length": 24}
{"curie": "MONDO:0009391", "names": ["hypermetabolism due to defect in mitochondria", "HYPERMETABOLISM DUE TO DEFECT IN MITOCHONDRIA", "Hypermetabolism due to Defect in Mitochondria", "hypermetabolism due to uncoupled mitochondrial oxidative phosphorylation 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypermetabolism due to defect in mitochondria", "shortest_name_length": 45}
{"curie": "UMLS:C5419071", "names": ["Locally Advanced Malignant Skin Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Malignant Skin Neoplasm", "shortest_name_length": 40}
{"curie": "MONDO:0004621", "names": ["upper lip cancer", "cancer of upper lip", "malignant upper lip neoplasm", "malignant neoplasm of upper lip", "Malig tumor of mucosa of upper lip", "Malig tumour of mucosa of upper lip", "Malignant tumor of upper labial mucosa", "Malignant tumour of upper labial mucosa", "Malignant neoplasm of upper lip, mucosa", "Malignant neoplasm of external upper lip", "Malignant neoplasm of mucosa of upper lip", "malignant neoplasm of upper labial mucosa", "Malignant neoplasm of upper lip, external", "Malignant tumor of oral aspect of upper lip", "lip neoplasm malignant upper, lipstick area", "Malignant tumour of oral aspect of upper lip", "Malignant tumor of inner aspect of upper lip", "Malignant neoplasm of upper lip, oral aspect", "Malignant tumour of inner aspect of upper lip", "lip neoplasm malignant of labial mucosa upper", "Malignant tumor of buccal aspect of upper lip", "Malignant tumor of lipstick area of upper lip", "Malignant neoplasm of upper lip, inner aspect", "Malignant tumour of buccal aspect of upper lip", "Malignant neoplasm of oral aspect of upper lip", "Malignant tumour of lipstick area of upper lip", "Malignant neoplasm of upper lip, buccal aspect", "Malignant neoplasm of upper lip, lipstick area", "malignant neoplasm of upper lip, lipstick area", "Malignant neoplasm of inner aspect of upper lip", "malignant neoplasm of inner aspect of upper lip", "Malignant neoplasm of buccal aspect of upper lip", "Malignant neoplasm of lipstick area of upper lip", "Malignant tumor of vermilion border of upper lip", "lip neoplasm malignant inner aspect of upper lip", "Malignant tumor of upper labial mucosa (disorder)", "Malignant tumour of vermilion border of upper lip", "Malignant neoplasm of upper lip, vermilion border", "Malignant neoplasm of vermilion border of upper lip", "malignant neoplasm of vermilion border of upper lip", "lip neoplasm malignant vermilion border of upper lip", "malignant neoplasm of upper labial mucosa (diagnosis)", "Malignant neoplasm of upper lip, lipstick area (disorder)", "malignant neoplasm of upper lip, lipstick area (diagnosis)", "malignant neoplasm of inner aspect of upper lip (diagnosis)", "Malignant tumor of vermilion border of upper lip (disorder)", "malignant neoplasm of vermilion border of upper lip (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "upper lip cancer", "shortest_name_length": 16}
{"curie": "MONDO:0012672", "names": ["GBD4", "cholelith", "gallstone", "gallstones", "Gallstones", "GALL STONE", "GALLSTONES", "Gallstone(s)", "Cholelithiases", "BILIARY STONES", "CHOLELITHIASIS", "cholelithiasis", "Cholelithiasis", "Biliary stones", "cholelithiases", "Stone - biliary", "Calculus biliary", "Biliary calculus", "Gallstone Disease", "gallstone disease", "gallbladder stone", "Calculus - biliary", "Gallstone Diseases", "gallbladder stones", "Cholelithiasis, NOS", "CL - Cholelithiasis", "cholecystolithiasis", "gallbladder calculus", "GALLBLADDER DISEASE 4", "Gallbladder Disease 4", "gallbladder disease 4", "calculus of gallbladder", "Calculus in biliary tract", "gallbladder disease type 4", "biliary tract disease calculus", "gallbladder calculus (diagnosis)", "Calculus in biliary tract (disorder)", "Calculus in biliary tract (diagnosis)", "Calculus of bile duct without mention of cholecystitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholelithiasis", "shortest_name_length": 4}
{"curie": "MONDO:0021090", "names": ["breast lipid-rich carcinoma", "Breast Lipid-Rich Carcinoma", "Lipid-Rich Breast Carcinoma", "lipid-rich breast carcinoma", "lipid-rich carcinoma of breast", "Lipid Secreting Breast Carcinoma", "lipid secreting breast carcinoma", "lipid-rich carcinoma of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lipid-rich breast carcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C4525617", "names": ["Stage III Duodenal Neuroendocrine Tumor", "Stage III Duodenal Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Duodenal Neuroendocrine Tumor AJCC v8", "shortest_name_length": 39}
{"curie": "MONDO:0042494", "names": ["childhood melanoma", "Childhood Melanoma", "Melanoma of childhood", "childhood malignant melanoma", "childhood melanoma (disease)", "pediatric melanoma (disease)", "malignant melanoma, childhood", "melanoma (disease) of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood malignant melanoma", "shortest_name_length": 18}
{"curie": "MONDO:0011164", "names": ["MHS6", "Mhs6", "malignant hyperthermia susceptibility 6", "malignant hyperthermia susceptibility type 6", "MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 6", "Malignant hyperpyrexia susceptibility type 6", "Malignant hyperthermia susceptibility type 6", "malignant hyperthermia, susceptibility to, 6", "malignant hyperpyrexia susceptibility type 6", "malignant hyperthermia, susceptibility to, type 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant hyperthermia, susceptibility to, 6", "shortest_name_length": 4}
{"curie": "MONDO:0018010", "names": ["JIIM", "juvenile idiopathic inflammatory myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile idiopathic inflammatory myopathy", "shortest_name_length": 4}
{"curie": "UMLS:C0752306", "names": ["Brain Anoxia Ischemia", "Brain Ischemia Anoxia", "Brain Anoxia-Ischemia", "Brain Ischemia-Anoxia", "Ischemia-Anoxia, Brain", "Anoxia Ischemia, Brain", "Brain Ischemia-Anoxias", "Brain Anoxia-Ischemias", "Ischemia Anoxia, Brain", "Anoxia-Ischemia, Brain", "Anoxia-Ischemias, Brain", "Ischemia-Anoxias, Brain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anoxia-Ischemia, Brain", "shortest_name_length": 21}
{"curie": "UMLS:C5420315", "names": ["Unresectable Hereditary Thyroid Gland Medullary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Hereditary Thyroid Gland Medullary Carcinoma", "shortest_name_length": 57}
{"curie": "MONDO:0010923", "names": ["Proximal Myopathy with Focal Depletion of Mitochondria", "proximal myopathy with focal depletion of mitochondria", "Proximal myopathy with focal depletion of mitochondria", "PROXIMAL MYOPATHY WITH FOCAL DEPLETION OF MITOCHONDRIA", "Proximal myopathy with focal depletion of mitochondria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "proximal myopathy with focal depletion of mitochondria", "shortest_name_length": 54}
{"curie": "MONDO:0005366", "names": ["chronic hep b", "chronic Hepatitis B", "Chronic hepatitis B", "chronic hepatitis b", "hepatitis b chronic", "Chronic Hepatitis B", "HEPATITIS B CHRONIC", "hepatitis B, chronic", "Hepatitis B, Chronic", "Chronic viral hepatitis B", "HEPATITIS, CHRONIC TYPE B", "hepatitis b chronic viral", "chronic hepatitis, B virus", "Chronic (viral) hepatitis B", "chronic hepatitis B infection", "Chronic type B viral hepatitis", "hepatitis B infection, chronic", "hepatitis; virus, chronic, type B", "Chronic Hepatitis B Virus Infection", "chronic hepatitis B virus infection", "chronic viral hepatitis B infection", "Hepatitis B Virus Infection, Chronic", "chronic hepatitis B infection (diagnosis)", "Chronic type B viral hepatitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic hepatitis B virus infection", "shortest_name_length": 13}
{"curie": "UMLS:C0543858", "names": ["Secondary Motor Neuron Disease", "Motor neuron disease, secondary", "Motor Neuron Disease, Secondary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Motor Neuron Disease, Secondary", "shortest_name_length": 30}
{"curie": "UMLS:C0524730", "names": ["Odontome", "Odontomes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Odontome", "shortest_name_length": 8}
{"curie": "MONDO:0008059", "names": ["NFJS", "Nfj syndrome", "NFJ syndrome", "NFJ SYNDROME", "NAEGELI syndrome", "NAEGELI SYNDROME", "Naegeli syndrome", "Naegeli's syndrome", "Franceschetti-Jadassohn syndrome", "Naegeli-Franceschetti-Jadassohn Syndrome", "Naegeli-Franceschetti-Jadassohn syndrome", "NAEGELI-Franceschetti-Jadassohn syndrome", "NAEGELI-FRANCESCHETTI-JADASSOHN SYNDROME", "Naegeli-Franceschetti-Jadassohn syndrome (disorder)", "Naegeli-Franceschetti-Jadassohn syndrome (diagnosis)", "reticular skin changes, dental anomalies, decreased function of sweat glands, strabismus, and optic atrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Naegeli-Franceschetti-Jadassohn syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0019909", "names": ["R16", "Ring 16", "chromosome 16 ring", "ring chromosome 16", "Ring chromosome 16", "Ring chromosome type 16", "Ring chromosome 16 syndrome", "Ring chromosome 16 syndrome (disorder)", "Ring chromosome 16 syndrome (diagnosis)", "anomaly of chromosome pair ring chromosome 16 syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ring chromosome 16", "shortest_name_length": 3}
{"curie": "MONDO:0004412", "names": ["Spiradenocarcinoma", "malignant spiradenoma", "Malignant spiradenoma", "Malignant Spiradenoma", "spiradenoma, malignant", "Malignant eccrine spiradenoma", "Malignant Eccrine Spiradenoma", "malignant eccrine spiradenoma", "Carcinoma ex Eccrine Spiradenoma", "malignant eccrine spiradenoma of skin", "Malignant eccrine spiradenoma of skin", "Malignant eccrine spiradenoma of skin (disorder)", "malignant eccrine spiradenoma of skin (diagnosis)", "Malignant eccrine spiradenoma (morphologic abnormality)", "malignant eccrine spiradenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant spiradenoma", "shortest_name_length": 18}
{"curie": "MONDO:0002438", "names": ["acquired polycythemia", "secondary polycythemia", "Polycythemia, secondary", "polycythemia, secondary", "acquired polycythemia (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired polycythemia", "shortest_name_length": 21}
{"curie": "MONDO:0021243", "names": ["Parotid Tumor", "parotid tumor", "Tumor of Parotid", "parotid neoplasm", "tumor of parotid", "Parotid Neoplasm", "parotid gland tumor", "neoplasm of parotid", "Neoplasm of Parotid", "Parotid Gland Tumor", "tumor of the parotid", "Tumor of the Parotid", "Parotid Gland Neoplasm", "Tumor of Parotid Gland", "parotid gland neoplasm", "tumor of parotid gland", "Neoplasm of the Parotid", "neoplasm of the parotid", "neoplasm of parotid gland", "Neoplasm of Parotid Gland", "tumor of the parotid gland", "Tumor of the Parotid Gland", "Neoplasm of the Parotid Gland", "neoplasm of the parotid gland", "parotid gland neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parotid gland neoplasm", "shortest_name_length": 13}
{"curie": "UMLS:C2064429", "names": ["Extrahepatic Bile Duct Adenocarcinoma, Intestinal Type", "intestinal type adenocarcinoma of extrahepatic bile duct", "extrahepatic bile duct malignant adenocarcinoma intestinal type", "intestinal type adenocarcinoma of extrahepatic bile duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intestinal type adenocarcinoma of extrahepatic bile duct", "shortest_name_length": 54}
{"curie": "UMLS:C0854437", "names": ["Bladder Granuloma", "Bladder granuloma", "Urinary Bladder Granuloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder granuloma", "shortest_name_length": 17}
{"curie": "UMLS:C0278807", "names": ["Gallbladder Cancer Unresectable", "unresectable gallbladder cancer", "Unresectable Gallbladder Cancer", "gallbladder cancer, unresectable", "Unresectable Gallbladder Carcinoma", "Unresectable Cancer of Gallbladder", "Gallbladder Carcinoma Unresectable", "Unresectable Cancer of the Gallbladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Gallbladder Carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0005178", "names": ["oa", "OA", "a o", "o a", "oas", "DJD", "arthrosis", "primary OA", "osteoarthrosis", "Osteoarthritis", "Osteoarthrosis", "OSTEOARTHRITIS", "osteoarthritis", "OSTEOARTHROSIS", "Osteoarthroses", "Osteoarthritides", "oa osteoarthritis", "Osteoarthritis NOS", "OA - Osteoarthritis", "OA - Osteoarthrosis", "Osteoarthritis, NOS", "Osteoarthrosis (OA)", "Osteoarthrosis, NOS", "ARTHRITIS, SENESCENT", "joint(s) degeneration", "joint; osteoarthrosis", "Degeneration;joint(s)", "Arthritis;degenerative", "arthritis; hypertrophy", "Degenerative arthritis", "hypertrophy; arthritis", "degenerative arthritis", "Hypertrophic arthritis", "arthritis degenerative", "Degenerative Arthritis", "hypertrophic arthritis", "Arthritis, Degenerative", "obsolete_osteoarthritis", "ARTHRITIS, HYPERTROPHIC", "ARTHRITIS OSTEOARTHRITIS", "degenerative arthropathy", "Degenerative arthropathy", "Degenerative Arthritides", "arthritis osteoarthritis", "osteoarthritis arthritis", "Osteoarthritis (M15-M19)", "Arthritides, Degenerative", "Osteoarthritis (disorder)", "ARTHROPATHY, DEGENERATIVE", "DEGENERATIVE JOINT DISEASE", "osteoarthritis (diagnosis)", "degenerative joint disease", "Hypertrophic polyarthritis", "Degenerative joint disease", "degenerative disease joint", "Degenerative polyarthritis", "Degenerative Joint Disease", "osteoarthrosis (diagnosis)", "Degenerative arthritis, NOS", "Osteoarthritis;degenerative", "JOINT DISEASE, DEGENERATIVE", "degenerative osteoarthritis", "osteoarthritis degenerative", "degenerative diseases joint", "degenerative disease joints", "Hypertrophic arthritis, NOS", "Osteoarthritis, degenerative", "Degenerative arthropathy, NOS", "Degenerative polyarthritis, NOS", "Degenerative joint disease, NOS", "Hypertrophic polyarthritis, NOS", "Osteoarthritis, unspecified site", "Osteoarthrosis and allied disorder", "osteoarthrosis and allied disorder", "Degenerative polyarthritis (disorder)", "Osteoarthrosis, unspecified whether generalized or localized", "Osteoarthrosis, localized, not specified whether primary or secondary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteoarthritis", "shortest_name_length": 2}
{"curie": "MONDO:0030025", "names": ["NEDHYMS", "neurodevelopmental disorder with hypotonia, microcephaly, and seizures", "NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, MICROCEPHALY, AND SEIZURES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with hypotonia, microcephaly, and seizures", "shortest_name_length": 7}
{"curie": "MONDO:0019046", "names": ["HLD", "leucodystrophy", "leukodystrophy", "Leucodystrophy", "Leukodystrophy", "leucodystrophies", "leukodystrophies", "Leukodystrophies", "Leukodystrophy NOS", "Leukodystrophy, NOS", "Leukodystrophy (disorder)", "hypomyelinating leukodystrophy", "leukodystrophy, hypomyelinating", "hypomyelinating leukoencephalopathy", "Degeneration of white matter of brain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukodystrophy", "shortest_name_length": 3}
{"curie": "UMLS:C4682964", "names": ["Urethral Cancer by AJCC v7 Stage", "Urethral Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urethral Cancer by AJCC v7 Stage", "shortest_name_length": 32}
{"curie": "MONDO:0019789", "names": ["CHP", "Winkelmann cytophagic panniculitis", "Cytophagic histiocytic panniculitis", "cytophagic histiocytic panniculitis", "Cytophagic histiocytic panniculitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cytophagic histiocytic panniculitis", "shortest_name_length": 3}
{"curie": "MONDO:0012746", "names": ["CMD2A", "dilated cardiomyopathy 2A", "CARDIOMYOPATHY, DILATED, 2A", "cardiomyopathy, dilated, 2A", "Cardiomyopathy, Dilated, 2a", "dilated cardiomyopathy type 2A", "cardiomyopathy, dilated, type 2A", "CARDIOMYOPATHY, DILATED, AUTOSOMAL RECESSIVE", "cardiomyopathy, dilated, autosomal recessive", "CARDIOMYOPATHY, CONGESTIVE, AUTOSOMAL RECESSIVE", "cardiomyopathy, congestive, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 2A", "shortest_name_length": 5}
{"curie": "UMLS:C5243703", "names": ["Immune-mediated hepatic disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immune-mediated hepatic disorder", "shortest_name_length": 32}
{"curie": "UMLS:C5239044", "names": ["High Risk Prostate Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Risk Prostate Carcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0010356", "names": ["NSIAD", "NEPHROGENIC SYNDROME OF INAPPROPRIATE ANTIDIURESIS", "Nephrogenic syndrome of inappropriate antidiuresis", "nephrogenic syndrome of inappropriate antidiuresis", "Nephrogenic Syndrome of Inappropriate Antidiuresis", "NSIAD - nephrogenic syndrome of inappropriate antidiuresis", "Nephrogenic syndrome of inappropriate antidiuresis (disorder)", "nephrogenic syndrome of inappropriate antidiuresis, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrogenic syndrome of inappropriate antidiuresis", "shortest_name_length": 5}
{"curie": "MONDO:0014671", "names": ["CMT6B", "HMSN6B", "HMSN 6B", "HMSN VIB", "Charcot-Marie-Tooth disease, type 6B", "CHARCOT-MARIE-TOOTH DISEASE, TYPE 6B", "neuropathy, hereditary motor and sensory, type 6B", "NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB", "neuropathy, hereditary motor and sensory, type VIB", "SLC25A46 hereditary motor and sensory neuropathy type 6", "NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB, WITH OPTIC ATROPHY", "hereditary motor and sensory neuropathy type 6 caused by mutation in SLC25A46"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuropathy, hereditary motor and sensory, type 6B", "shortest_name_length": 5}
{"curie": "MONDO:0035647", "names": ["Childhood-onset Steinert disease", "Childhood-onset myotonic dystrophy type 1", "childhood-onset Steinert myotonic dystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood-onset Steinert myotonic dystrophy", "shortest_name_length": 32}
{"curie": "UMLS:C4526612", "names": ["Stage IV Thymoma", "Stage IV Thymoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Thymoma AJCC v8", "shortest_name_length": 16}
{"curie": "MONDO:0009448", "names": ["iminoglycinuria", "Iminoglycinuria", "IMINOGLYCINURIA", "Iminoglycinuria, NOS", "iminoglycinuria, digenic", "Iminoglycinuria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "iminoglycinuria", "shortest_name_length": 15}
{"curie": "UMLS:C0558385", "names": ["disease neck", "Neck Disease", "neck disease", "neck disorder", "Neck Disorder", "disorder neck", "diseases neck", "disorders neck", "disease of neck", "disorder of neck", "Disorder of neck", "Disorder of neck (disorder)", "disorder of neck (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disorder of neck", "shortest_name_length": 12}
{"curie": "UMLS:C0269014", "names": ["cavernosal fibrosis", "corpus cavernosum; fibrosis", "fibrosis; corpus cavernosum", "Fibrosis of corpus cavernosum", "cavernosal fibrosis (diagnosis)", "Fibrosis of the corpora cavernosa", "Fibrosis of corpus cavernosum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fibrosis of corpus cavernosum", "shortest_name_length": 19}
{"curie": "MONDO:0024429", "names": ["alice in wonderland syndrome", "Alice in Wonderland syndrome", "Alice in wonderland syndrome", "Alice in Wonderland Syndrome", "syndrome alice in wonderland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alice in Wonderland syndrome", "shortest_name_length": 28}
{"curie": "UMLS:C5401097", "names": ["HAMN", "High Grade Appendix Mucinous Neoplasm", "High-Grade Appendix Mucinous Neoplasm", "High Grade Appendix Mucinous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Appendix Mucinous Neoplasm", "shortest_name_length": 4}
{"curie": "MONDO:0011595", "names": ["COIF", "NDNC7", "COIF syndrome", "Iso-Kikuchi syndrome", "congenital isolated nail dysplasia", "isolated congenital nail dysplasia", "Isolated congenital nail dysplasia", "Congenital Isolated nail dysplasia", "Congenital isolated onychodysplasia", "Nail dysplasia, isolated congenital", "Isolated congenital onychodysplasia", "isolated congenital onychodysplasia", "nail dysplasia, isolated congenital", "ONYCHODYSPLASIA, ISOLATED CONGENITAL", "onychodysplasia, isolated congenital", "Onychodysplasia, Isolated Congenital", "nonsyndromic congenital nail disorder 7", "NAIL DISORDER, NONSYNDROMIC CONGENITAL, 7", "nail disorder, nonsyndromic congenital, 7", "Congenital onychodysplasia of index fingers", "nonsyndromic congenital nail disorder type 7", "Congenital isolated onychodysplasia (disorder)", "congenital onychodysplasia of the index fingers", "Congenital onychodysplasia of the index fingers", "Congenital onychodysplasia of index fingers (disorder)", "COIF (congenital onychodysplasia of index fingers) syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nonsyndromic congenital nail disorder 7", "shortest_name_length": 4}
{"curie": "MONDO:0009271", "names": ["GO", "Walt Disney dwarfism", "WALT DISNEY DWARFISM", "Osteodysplastic geroderma", "Geroderma osteodysplastica", "geroderma osteodysplastica", "Gerodermia osteodysplastica", "Geroderma osteodysplasticum", "GERODERMIA OSTEODYSPLASTICA", "Geroderma Osteodysplasticum", "gerodermia osteodysplastica", "geroderma osteodysplasticum", "GERODERMA OSTEODYSPLASTICUM", "GO - Geroderma osteodysplastica", "Geroderma osteodysplastica (disorder)", "Geroderma osteodysplastica hereditaria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "geroderma osteodysplastica", "shortest_name_length": 2}
{"curie": "UMLS:C1334051", "names": ["HPVA Cervical Carcinoma", "HPV-Related Cervical Carcinoma", "HPV-Associated Cervical Carcinoma", "Human Papillomavirus-Related Cervical Carcinoma", "Human Papilloma Virus-Related Cervical Carcinoma", "Human Papilloma Virus Related Cervical Carcinoma", "Human Papillomavirus (HPV)-Related Cervical Cancer", "Human Papillomavirus-Associated Cervical Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Human Papillomavirus-Related Cervical Carcinoma", "shortest_name_length": 23}
{"curie": "EFO:0008537", "names": ["anti-topoisomerase-I-antibody-positive systemic scleroderma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anti-topoisomerase-I-antibody-positive systemic scleroderma", "shortest_name_length": 59}
{"curie": "UMLS:C0278729", "names": ["stage 0 vulva cancer", "VULVAR CANCER IN SITU", "Stage 0 Vulvar Cancer", "stage 0 vulvar cancer", "vulva cancer, stage 0", "Vulval cancer stage 0", "Vulvar cancer in situ", "vulvar cancer in situ", "vulvar cancer, stage 0", "Cancer in situ of vulva", "Carcinoma in situ, vulva", "Stage 0 Vulvar Carcinoma", "Carcinoma in situ of vulva", "carcinoma in situ of vulva", "stage 0 cancer of the vulva", "cancer of the vulva, stage 0", "FIGO Stage 0 Vulva Carcinoma", "Stage 0 Vulval Cancer AJCC v6", "Stage 0 Vulvar Cancer AJCC v6", "AJCC Stage 0 Vulvar Cancer v6", "Vulvar Cancer Stage 0 AJCC v6", "carcinoma in situ of the vulva", "stage 0 carcinoma of the vulva", "Vulva Carcinoma in situ AJCC v6", "carcinoma of the vulva, stage 0", "Carcinoma in situ of vulva, NOS", "Stage 0 Vulvar Carcinoma AJCC v6", "Stage 0 Vulval Carcinoma AJCC v6", "Vulvar Carcinoma in situ AJCC v6", "vulvar neoplasm carcinoma in situ", "Carcinoma in situ of Vulva AJCC v6", "Carcinoma in situ of vulva (disorder)", "FIGO Stage 0 Vulvar Carcinoma AJCC v6", "Carcinoma in situ of the Vulva AJCC v6", "carcinoma in situ of vulva (diagnosis)", "FIGO Stage 0 Carcinoma of Vulva AJCC v6", "FIGO Stage 0 Carcinoma of the Vulva AJCC v6", "Vulvar intraepithelial neoplasia III [VIN III]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Vulvar Carcinoma", "shortest_name_length": 20}
{"curie": "MONDO:0002419", "names": ["Transient Tic Disorder", "Transient tic disorder", "transient tic disorder", "transient tic disorders", "Transient Tic Disorders", "Tic Disorder, Transient", "Tic Disorders, Transient", "Transient tic disorder, NOS", "benign Tic disorder of childhood", "Benign Tic Disorder of Childhood", "Transient tic disorder (disorder)", "transient tic disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transient tic disorder", "shortest_name_length": 22}
{"curie": "UMLS:C5670411", "names": ["Unresectable Ovarian Endometrioid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Ovarian Endometrioid Adenocarcinoma", "shortest_name_length": 48}
{"curie": "MONDO:0007120", "names": ["aniridia absent patella", "Aniridia and Absent Patella", "aniridia and absent patella", "ANIRIDIA AND ABSENT PATELLA", "Aniridia-absent patella syndrome", "aniridia-absent patella syndrome", "Aniridia and absent patella syndrome", "Aniridia and absent patella syndrome (disorder)", "familial syndrome of aniridia and absence of the patella"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aniridia-absent patella syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0016441", "names": ["Acquired PXE", "acquired PXE", "Acquired pseudoxanthoma elasticum", "acquired pseudoxanthoma elasticum", "Acquired pseudoxanthoma elasticum (disorder)", "Acquired Gronblad-Strandberg-Touraine syndrome", "acquired Gronblad-Strandberg-Touraine syndrome", "localized acquired cutaneous pseudoxanthoma elasticum", "acquired pseudoxanthoma elasticum (inherited or acquired)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired pseudoxanthoma elasticum", "shortest_name_length": 12}
{"curie": "UMLS:C0038826", "names": ["Suprainfection", "Superinfection", "superinfection", "SUPERINFECTION", "Superinfections", "superinfections", "Superadded infection", "Superimposed infection", "superimposed infection", "Infection superimposed", "INFECTION SUPERIMPOSED", "Microbial Superinvasion", "Microbial Superinvasions", "Superinvasion, Microbial", "Superinvasions, Microbial", "Superadded infection present", "Superimposed infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Superinfection", "shortest_name_length": 14}
{"curie": "UMLS:C0751885", "names": ["Slow Channel Congenital Myasthenic Syndrome", "Congenital Slow-Channel Myasthenic Syndrome", "Slow-Channel Congenital Myasthenic Syndrome", "Congenital Slow Channel Myasthenic Syndrome", "Congenital Slow-Channel Myasthenic Syndromes", "Slow-Channel Congenital Myasthenic Syndromes", "Slow Channel Congenital Myasthenic Syndromes", "Congenital Slow Channel Myasthenic Syndromes", "Myasthenic Syndrome, Congenital, Slow-Channel", "Myasthenic Syndromes, Congenital, Slow Channel"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myasthenic Syndromes, Congenital, Slow Channel", "shortest_name_length": 43}
{"curie": "MONDO:0016514", "names": ["Kallin syndrome", "Gamborg-Nielsen syndrome", "epidermolysis bullosa simplex with anodontia/hypodontia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolysis bullosa simplex with anodontia/hypodontia", "shortest_name_length": 15}
{"curie": "MONDO:0005682", "names": ["BRONCHOPNEUMONIA", "Bronchopneumonia", "bronchopneumonia", "Lobular pneumonia", "Lobular Pneumonia", "lobular pneumonia", "Bronchopneumonias", "bronchial pneumonia", "pneumonia bronchial", "Bronchial Pneumonia", "Bronchial pneumonia", "Pneumonia;bronchial", "bronchus; pneumonia", "Bronchial Pneumonias", "pneumonia; bronchial", "Pneumonia, Bronchial", "Bronchopneumonia NOS", "Pneumonias, Bronchial", "Bronchopneumonia, NOS", "Bronchopneumonia (disorder)", "bronchopneumonia (diagnosis)", "Bronchopneumonia, unspecified", "chest infection - bronchopneumonia", "Chest infection - bronchopneumonia", "Bronchopneumonia, organism unspecified", "Bronchopneumonia, unspecified organism", "chest infection - unspecified bronchopneumonia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bronchopneumonia", "shortest_name_length": 16}
{"curie": "MONDO:0012564", "names": ["Polyosteolysis-hyperostosis syndrome", "POLYOSTEOLYSIS-HYPEROSTOSIS SYNDROME", "Polyosteolysis/hyperostosis syndrome", "Polyosteolysis-Hyperostosis Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Polyosteolysis-hyperostosis syndrome", "shortest_name_length": 36}
{"curie": "UMLS:C1336003", "names": ["Small Intestinal Mantle Cell Lymphoma", "Mantle Cell Lymphoma of Small Intestine", "mantle cell lymphoma of small intestine", "Mantle Cell Lymphoma of the Small Intestine", "mantle cell lymphoma of small intestine (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mantle cell lymphoma of small intestine", "shortest_name_length": 37}
{"curie": "MONDO:0019493", "names": ["adult heart tumor", "Adult heart tumor", "Adult heart tumour", "adult cardiac tumor", "Adult cardiac tumor", "Adult cardiac tumour", "primary adult heart tumor", "Primary adult heart tumor", "Adult heart tumor (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary adult heart tumor", "shortest_name_length": 17}
{"curie": "MONDO:0021109", "names": ["IUP", "inverted urothelial papilloma", "Inverted urothelial papilloma", "Inverted Urothelial Papilloma", "urothelium inverted papilloma", "Urinary Tract Inverted Papilloma", "urinary tract inverted papilloma", "inverted papilloma of urinary tract", "Inverted Papilloma of Urinary Tract", "Inverted urothelial papilloma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inverted urothelial papilloma", "shortest_name_length": 3}
{"curie": "DOID:0080707", "names": ["Medulloblastoma, group 3", "medulloblastoma non-WNT/non-SHH group 3", "Medulloblastoma, Non-WNT/Non-SHH, Group 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "medulloblastoma non-WNT/non-SHH group 3", "shortest_name_length": 24}
{"curie": "UMLS:C0796549", "names": ["recurrent PNET", "recurrent pPNET", "PNET, recurrent", "pPNET, recurrent", "Recurrent Askin Tumor", "Recurrent Askin's Tumor", "recurrent Ewing sarcoma/PNET", "recurrent Ewing's sarcoma/PNET", "Recurrent Tumors of Ewing's Family", "Recurrent tumors of the Ewing's family", "recurrent neuroepithelioma, peripheral", "Recurrent Tumors of the Ewing's Family", "recurrent tumors of the Ewing's family", "neuroepithelioma, recurrent, peripheral", "recurrent peripheral neuroectodermal tumor", "peripheral neuroectodermal tumor, recurrent", "recurrent primitive neuroectodermal tumor (PNET)", "primitive neuroectodermal tumor (PNET), recurrent", "recurrent Ewing sarcoma/primitive neuroectodermal tumor", "recurrent Ewing's sarcoma/primitive neuroectodermal tumor", "Recurrent Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor", "recurrent Ewing sarcoma/peripheral primitive neuroectodermal tumor", "Recurrent Ewing's Sarcoma/Peripheral Primitive Neuroectodermal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent tumors of the Ewing's family", "shortest_name_length": 14}
{"curie": "MONDO:0100419", "names": ["AML, KIT exon 8 mutation", "AML, c-KIT Exon 8 Mutation", "AML, CD117 Exon 8 Mutation", "acute myeloid leukemia, KIT exon 8 mutation", "AML, KIT Proto-Oncogene Tyrosine Protein Kinase Gene Exon 8 Mutation", "AML, v-Kit Hardy-Zuckerman 4 Feline Sarcoma Viral Oncogene Homolog Gene Exon 8 Mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, KIT exon 8 mutation", "shortest_name_length": 24}
{"curie": "MONDO:0012330", "names": ["talo-patello-scaphoid osteolysis", "singh-Williams-McAlister syndrome", "TALO-PATELLO-SCAPHOID OSTEOLYSIS, SYNOVITIS, AND SHORT FOURTH METACARPALS", "talo-patello-scaphoid osteolysis, synovitis, and short fourth metacarpals", "Talo-patello-scaphoid osteolysis, synovitis, and short fourth metacarpals"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "talo-patello-scaphoid osteolysis", "shortest_name_length": 32}
{"curie": "UMLS:C0751641", "names": ["Symptomatic Partial Complex Epilepsy", "Partial Complex Epilepsy, Symptomatic", "Epilepsy, Symptomatic, Partial Complex"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epilepsy, Symptomatic, Partial Complex", "shortest_name_length": 36}
{"curie": "MONDO:0006509", "names": ["papillary carcinoma", "Papillary Carcinoma", "Papillary carcinoma", "carcinoma papillary", "papillary carcinomas", "Carcinoma, Papillary", "Papillary Carcinomas", "Carcinomas, Papillary", "Papillary carcinoma NOS", "Papillary carcinoma, NOS", "papillary carcinoma (diagnosis)", "Papillary carcinoma (morphologic abnormality)", "papillary carcinoma (morphologic abnormality)", "papillary carcinoma NOS (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papillary carcinoma", "shortest_name_length": 19}
{"curie": "UMLS:C4288108", "names": ["Tracheoarterial Fistula"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tracheoarterial Fistula", "shortest_name_length": 23}
{"curie": "UMLS:C0333868", "names": ["Severe Cytologic Atypia", "Severe cytologic atypia", "Severe cytologic atypia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Severe cytologic atypia", "shortest_name_length": 23}
{"curie": "MONDO:0002867", "names": ["Cystadenocarcinoma pancreas", "pancreas cystadenocarcinoma", "PANCREAS, CYSTADENOCARCINOMA", "pancreatic cystadenocarcinoma", "Pancreatic Cystadenocarcinoma", "cystadenocarcinoma - pancreas", "Cystadenocarcinoma - pancreas", "Cystadenocarcinoma of Pancreas", "Cystadenocarcinoma of pancreas", "cystadenocarcinoma of pancreas", "Cystadenocarcinoma of the pancreas", "Cystadenocarcinoma of the Pancreas", "cystadenocarcinoma of the pancreas", "Cystadenocarcinoma of pancreas (disorder)", "cystadenocarcinoma of pancreas (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic cystadenocarcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C4682579", "names": ["Stage IA Uterine Corpus Adenosarcoma", "Stage IA Uterine Corpus Adenosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Uterine Corpus Adenosarcoma AJCC v8", "shortest_name_length": 36}
{"curie": "MONDO:0008582", "names": ["HND", "TNS", "ECTD3", "WITKOP SYNDROME", "WITKOP syndrome", "Witkop syndrome", "Witkop Syndrome", "Witkop's disease", "Witkop's syndrome", "Whitkop's syndrome", "tooth and nail syndrome", "Tooth and Nail Syndrome", "Tooth and nail syndrome", "TOOTH-AND-NAIL SYNDROME", "tooth-and-nail syndrome", "Tooth-And-Nail Syndrome", "Hypodontia-Nail Dysplasia", "hypodontia-nail dysplasia", "hypodontia and nail dysplasia", "Hypodontia and Nail Dysplasia", "NAIL DYSPLASIA WITH HYPODONTIA", "nail dysplasia with hypodontia", "hypodontia with nail dysplasia", "Hypodontia with Nail Dysplasia", "Nail Dysplasia With Hypodontia", "Witkop-Brearley-Gentry syndrome", "hypodontia - dysplasia of nails", "dysplasia of nails with hypodontia", "Dysplasia of nails with hypodontia", "hypodontia-nail dysgenesis syndrome", "Hypodontia-nail dysgenesis syndrome", "ECTODERMAL DYSPLASIA 3, WITKOP TYPE", "ectodermal dysplasia 3, Witkop type", "Hypodontia-dysplasia of nails syndrome", "hypodontia-dysplasia of nails syndrome", "ectodermal dysplasia 3, Tooth/nail type", "ECTODERMAL DYSPLASIA 3, TOOTH/NAIL TYPE", "Hypoplastic enamel-onycholysis-hypohidrosis syndrome", "hypoplastic enamel-onycholysis-hypohidrosis syndrome", "Hypoplastic enamel-onycholysis-hypohidrosis syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tooth and nail syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0004777", "names": ["laryngitis", "Laryngitis", "Acute Laryngitis", "laryngitis acute", "acute laryngitis", "Acute laryngitis", "LARYNGITIS ACUTE", "Laryngitis;acute", "laryngitis, acute", "LARYNGITIS, ACUTE", "Laryngitis (acute)", "Acute laryngitis NOS", "Laryngitis acute NOS", "Laryngitis (acute) NOS", "Acute laryngitis (disorder)", "acute laryngitis (diagnosis)", "acute laryngitis with obstruction", "Acute laryngitis with obstruction", "laryngitis acute with obstruction", "Acute laryngitis with obstruction (disorder)", "acute laryngitis with obstruction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute laryngitis", "shortest_name_length": 10}
{"curie": "UMLS:C0435630", "names": ["Fracture of wrist", "fracture radius and ulna distal end", "Fracture of distal end of radius and ulna", "Fracture of lower end of both ulna and radius", "Fracture of distal end of radius and ulna (disorder)", "Fracture of distal end of radius and ulna (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fracture of distal end of radius and ulna", "shortest_name_length": 17}
{"curie": "MONDO:0013387", "names": ["DEE7", "EIEE7", "KCNQ2-NEE", "KCNQ2-related disorders", "KCNQ2-related epileptic encephalopathy", "early infantile epileptic encephalopathy 7", "epileptic encephalopathy, early infantile, 7", "developmental and epileptic encephalopathy 7", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 7", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7", "developmental and epileptic encephalopathy, 7", "KCNQ2-related neonatal epileptic encephalopathy", "epileptic encephalopathy, early infantile, type 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 7", "shortest_name_length": 4}
{"curie": "UMLS:C1333549", "names": ["FIGO Stage IA GTT", "FIGO Stage IA Gestational Trophoblastic Tumor", "FIGO Stage IA Gestational Trophoblastic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Stage IA Gestational Trophoblastic Tumor", "shortest_name_length": 17}
{"curie": "MONDO:0030800", "names": ["PFIC9", "cholestasis, progressive familial intrahepatic, 9", "CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholestasis, progressive familial intrahepatic, 9", "shortest_name_length": 5}
{"curie": "UMLS:C4727376", "names": ["Recurrent Breast Paget Disease", "Recurrent Paget Disease of the Breast", "Recurrent Paget's Disease of the Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Breast Paget Disease", "shortest_name_length": 30}
{"curie": "MONDO:0002599", "names": ["teratocarcinoma", "Teratocarcinoma", "Teratocarcinomas", "teratocarcinoma (diagnosis)", "Mixed embryonal carcinoma and teratoma", "mixed embryonal carcinoma and teratoma", "Mixed Embryonal Carcinoma and Teratoma", "mixed Embryonal carcinoma and teratoma", "Teratocarcinoma (morphologic abnormality)", "teratocarcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "teratocarcinoma", "shortest_name_length": 15}
{"curie": "UMLS:C0266679", "names": ["Cebocephaly", "cebocephaly", "CEBOCEPHALY", "cebocephalus", "Cebocephalus", "Cebocephaly (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cebocephaly", "shortest_name_length": 11}
{"curie": "MONDO:0003067", "names": ["Cervical adenitis", "CERVICAL ADENITIS", "adenitis cervical", "cervical adenitis", "Adenitis cervical", "cervical; adenitis", "adenitis; cervical", "Lymphadenitis cervical", "cervical lymphadenitis", "Cervical Lymphadenitis", "lymphadenitis cervical", "Cervical lymphadenitis", "LYMPHADENITIS, CERVICAL", "Lymphadenitis, cervical", "neck lymphadenitis (disease)", "lymphadenitis (disease) of neck", "Cervical lymphadenitis (disorder)", "Cervical lymphadenitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical lymphadenitis", "shortest_name_length": 17}
{"curie": "UMLS:C5551353", "names": ["death fear", "dying fear", "dying fears", "fear of dying", "death anxiety", "anxiety death", "Thanatophobia", "Fear of dying", "thanatophobia", "fear of death", "Fear of death", "Fear (of);death", "Fear (of);dying", "Fear About Death", "Fear of death/dying", "Fear of death (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fear of death", "shortest_name_length": 10}
{"curie": "UMLS:C5235855", "names": ["Advanced Renal Pelvis Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Renal Pelvis Carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0001295", "names": ["Idiopathic peripheral autonomic neuropathy", "idiopathic peripheral autonomic neuropathy", "neuropathy; peripheral, autonomic, idiopathic", "Idiopathic peripheral autonomic neuropathy NOS", "Idiopathic peripheral autonomic neuropathy (disorder)", "idiopathic peripheral autonomic neuropathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic peripheral autonomic neuropathy", "shortest_name_length": 42}
{"curie": "EFO:1001243", "names": ["wheat allergic reaction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "wheat allergic reaction", "shortest_name_length": 23}
{"curie": "UMLS:C1511322", "names": ["Breast Pleomorphic Adenoma", "Pleomorphic Adenoma of the Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Pleomorphic Adenoma", "shortest_name_length": 26}
{"curie": "UMLS:C0281790", "names": ["bone fistula", "Bone fistula", "fistula bone", "Bone Fistula", "fistula; bone", "bone; fistula"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone fistula", "shortest_name_length": 12}
{"curie": "MONDO:0001203", "names": ["Prolapse of lacrimal gland", "Lacrimal gland dislocation", "prolapse of lacrimal gland", "dislocation; lacrimal gland", "lacrimal gland; dislocation", "Dislocation of lacrimal gland", "dislocation of lacrimal gland", "Dislocation of lacrimal gland (disorder)", "dislocation of lacrimal gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prolapse of lacrimal gland", "shortest_name_length": 26}
{"curie": "MONDO:0003386", "names": ["Bladder Mesonephric Carcinoma", "Bladder Clear Cell Adenocarcinoma", "bladder clear cell adenocarcinoma", "Bladder Mesonephric Adenocarcinoma", "bladder mesonephric adenocarcinoma", "bladder Mesonephric adenocarcinoma", "clear cell adenocarcinoma of bladder", "Clear Cell Adenocarcinoma of Bladder", "Clear Cell Adenocarcinoma of the Bladder", "clear cell adenocarcinoma of the bladder", "urinary bladder clear cell adenocarcinoma", "Urinary Bladder Clear Cell Adenocarcinoma", "Clear Cell Adenocarcinoma of Urinary Bladder", "clear cell adenocarcinoma of urinary bladder", "clear cell adenocarcinoma of the urinary bladder", "Clear Cell Adenocarcinoma of the Urinary Bladder", "clear cell adenocarcinoma of bladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder clear cell adenocarcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0002165", "names": ["rectal tumor", "rectum tumor", "Rectal tumor", "Rectal Tumor", "Rectal tumour", "rectal tumors", "Rectal Tumors", "Tumor, Rectal", "Rectum--Tumors", "Tumor of Rectum", "rectal neoplasm", "Rectal Neoplasm", "Rectal neoplasm", "rectum neoplasm", "Tumor of rectum", "Rectum Neoplasm", "tumor of rectum", "Rectal Neoplasms", "Rectum Neoplasms", "Neoplasm, Rectal", "Neoplasm, Rectum", "rectal neoplasms", "Tumour of rectum", "Neoplasms, Rectal", "Neoplasm of rectum", "neoplasm of rectum", "Neoplasm of Rectum", "Rectal neoplasm NOS", "Tumor of the Rectum", "tumor of the rectum", "rectal tumor or cancer", "neoplasm of the rectum", "Neoplasm of the Rectum", "rectal benign neoplasm", "Neoplasm of the rectum", "rectum neoplasm (disease)", "Neoplasm of rectum (disorder)", "neoplasm of rectum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rectal neoplasm", "shortest_name_length": 12}
{"curie": "UMLS:C0338582", "names": ["Sporadic Cerebral Amyloid Angiopathy", "Sporadic cerebral amyloid angiopathy", "Sporadic cerebral amyloid angiopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sporadic Cerebral Amyloid Angiopathy", "shortest_name_length": 36}
{"curie": "UMLS:C4331227", "names": ["Recurrent Ependymal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Ependymal Tumor", "shortest_name_length": 25}
{"curie": "MONDO:0012343", "names": ["AAA2", "aortic aneurysm, familial abdominal 2", "Aortic Aneurysm, Familial Abdominal 2", "AORTIC ANEURYSM, FAMILIAL ABDOMINAL, 2", "aortic aneurysm, familial abdominal, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic aneurysm, familial abdominal, 2", "shortest_name_length": 4}
{"curie": "UMLS:C5420858", "names": ["Unresectable Kidney Medullary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Kidney Medullary Carcinoma", "shortest_name_length": 39}
{"curie": "MONDO:0000358", "names": ["orofacial cleft", "Orofacial cleft", "Orofacial cleft (disorder)", "Orofacial cleft (diagnosis)", "congenital malformations of mouth orofacial cleft"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orofacial cleft", "shortest_name_length": 15}
{"curie": "MONDO:0010457", "names": ["NATD", "OGDNS", "Ogden Syndrome", "Ogden syndrome", "OGDEN SYNDROME", "NAT1 deficiency", "Ogden syndrome (disorder)", "N-alpha-acetyltransferase", "N acetyltransferase deficiency", "arylamine n-acetyltransferase 1", "N acetyltransferase 1 deficiency", "N-terminal acetyltransferase deficiency", "N-TERMINAL ACETYLTRANSFERASE DEFICIENCY", "Acetyl-CoA:arylamine n-acetyltransferase", "Ogden syndrome, X-linked recessive, X-linked dominant", "X-linked malformation and infantile lethality syndrome", "X-linked Malformation and Infantile Lethality Syndrome", "Premature aging appearance-developmental delay-cardiac arrhythmia syndrome", "premature aging appearance-developmental delay-cardiac arrhythmia syndrome", "Premature aging appearance, developmental delay, cardiac arrhythmia syndrome", "Premature ageing appearance, developmental delay, cardiac arrhythmia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ogden syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C2347963", "names": ["Right Ventricular Outflow Tract Tachycardia", "Right Ventricular Outflow Tract Tachycardia by ECG Finding", "Right Ventricular Outflow Tract Tachycardia by EKG Finding"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Right Ventricular Outflow Tract Tachycardia by ECG Finding", "shortest_name_length": 43}
{"curie": "MONDO:0009532", "names": ["MDS", "MDCR", "MDLS", "agyria syndrome", "monosomy 17p13.3", "Monosomy 17p13.3", "Miller Dieker syndrome", "Lissencephaly syndrome", "Miller-Dieker syndrome", "miller-dieker syndrome", "Miller-Dieker Syndrome", "miller dieker syndrome", "Telomeric deletion 17p", "telomeric deletion 17p", "lissencephaly syndrome", "Miller Dieker Syndrome", "Syndrome, Miller-Dieker", "classical lissencephaly", "agyria-pachygyria syndrome", "Miller-Dieker Lissencephaly", "Lissencephaly, Miller Dieker", "Lissencephaly, Miller-Dieker", "Miller-Dieker syndrome (MDS)", "Miller Dieker syndrome (disorder)", "Miller-Dieker syndrome (diagnosis)", "CHROMOSOME 17p13.3 DELETION SYNDROME", "Chromosome 17p13.3 Deletion Syndrome", "chromosome 17P13.3 deletion syndrome", "MILLER-DIEKER LISSENCEPHALY SYNDROME", "Miller-Dieker Lissencephaly Syndrome", "Miller-Dieker lissencephaly syndrome", "Miller Dieker Lissencephaly Syndrome", "Lissencephaly Syndrome, Miller-Dieker", "Lissencephaly due to 17p13.3 deletion", "lissencephaly due to 17p13.3 deletion", "Syndrome, Miller-Dieker Lissencephaly", "Lissencephaly Syndrome, Miller Dieker", "MILLER-DIEKER SYNDROME CHROMOSOME REGION", "Miller-Dieker syndrome chromosome region", "Miller-Dieker lissencephaly syndrome (MDLS)", "hydrocephalic lissencephaly, is a major feature of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Miller-Dieker lissencephaly syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0035777", "names": ["PNAC", "parenteral nutrition-associated cholestasis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parenteral nutrition-associated cholestasis", "shortest_name_length": 4}
{"curie": "MONDO:0017325", "names": ["early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation", "shortest_name_length": 87}
{"curie": "MONDO:0007825", "names": ["incisors, rotation of upper central", "INCISORS, ROTATION OF UPPER CENTRAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "incisors, rotation of upper central", "shortest_name_length": 35}
{"curie": "UMLS:C1711232", "names": ["Nasopharyngeal Basaloid Carcinoma", "Nasopharyngeal Basaloid Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasopharyngeal Basaloid Carcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C0263008", "names": ["Skin fibrosis", "skin; fibrosis", "fibrosis; skin", "Dermal fibrosis", "Fibrosis of skin", "Skin fibrosis NOS", "Fibrosis of skin NOS", "Fibrosis of the skin", "Fibrotic disorder of skin", "Fibrosis of the skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fibrosis of the skin", "shortest_name_length": 13}
{"curie": "UMLS:C0561696", "names": ["Snake bite - wound", "Snake bite - wound (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Snake bite - wound", "shortest_name_length": 18}
{"curie": "MONDO:0005596", "names": ["Cystadenocarcinoma", "cystadenocarcinoma", "Cystadenocarcinomas", "cystadenocarcinomas", "Cystadenocarcinoma NOS", "Cystadenocarcinoma, NOS", "CYSTADENOCARCINOMA, MALIGNANT", "cystadenocarcinoma, malignant", "cystadenocarcinoma (diagnosis)", "cystadenocarcinoma (morphologic abnormality)", "Cystadenocarcinoma (morphologic abnormality)", "cystadenocarcinoma NOS (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cystadenocarcinoma", "shortest_name_length": 18}
{"curie": "MONDO:0011073", "names": ["DMTN", "TNDM", "Dmtn", "Tndm", "TNDM1", "Tndm1", "6q24-RELATED DIABETES MELLITUS", "Diabetes mellitus, transient neonatal 1", "diabetes mellitus, transient neonatal 1", "diabetes mellitus, transient neonatal, 1", "Diabetes Mellitus, Transient Neonatal, 1", "DIABETES MELLITUS, TRANSIENT NEONATAL, 1", "diabetes mellitus, transient neonatal, type 1", "Diabetes mellitus, transient neonatal 1 (disorder)", "K ATP Associated Transient Neonatal Diabetes Mellitus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diabetes mellitus, transient neonatal, 1", "shortest_name_length": 4}
{"curie": "MONDO:0021497", "names": ["benign cerebral tumor", "Benign Cerebral Tumor", "Benign cerebral tumor", "Benign cerebral tumour", "benign tumor of cerebrum", "Benign Tumor of Cerebrum", "Benign Cerebral Neoplasm", "benign cerebral neoplasm", "Benign neoplasm of cerebrum", "benign neoplasm of cerebrum", "Benign Neoplasm of Cerebrum", "benign tumor of the cerebrum", "Benign Tumor of the Cerebrum", "telencephalon benign neoplasm", "Benign Neoplasm of the Cerebrum", "benign neoplasm of the cerebrum", "Benign cerebral tumor (disorder)", "Benign neoplasm of cerebrum, NOS", "benign cerebral tumor (diagnosis)", "benign cerebral hemispheric tumor", "Benign Cerebral Hemispheric Tumor", "benign tumor of cerebral hemispheres", "Benign Tumor of Cerebral Hemispheres", "benign cerebral hemispheric neoplasm", "Benign Cerebral Hemispheric Neoplasm", "Benign Neoplasm of Cerebral Hemispheres", "benign neoplasm of cerebral hemispheres", "benign tumor of the cerebral hemispheres", "Benign Tumor of the Cerebral Hemispheres", "benign neoplasm of the cerebral hemispheres", "Benign Neoplasm of the Cerebral Hemispheres"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of cerebrum", "shortest_name_length": 21}
{"curie": "MONDO:0043209", "names": ["Albino", "albino", "ALBINISM", "Albinism", "albinism", "albinismus", "Albinismus", "Achromasia", "Albinism, NOS", "Albinismus, NOS", "Albinism (disorder)", "albinism (diagnosis)", "Albinism, unspecified", "albinism (physical finding)", "Achromasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "albinism", "shortest_name_length": 6}
{"curie": "MONDO:0010397", "names": ["Mecp2-Related Severe Neonatal Encephalopathy", "MECP2-related severe neonatal encephalopathy", "encephalopathy, neonatal severe, X-linked recessive", "neonatal severe encephalopathy due to MECP2 mutations", "severe neonatal encephalopathy due to MECP2 mutations", "Severe Neonatal Encephalopathy Due to MECP2 Mutations", "ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATION", "severe congenital encephalopathy due to MECP2 mutation", "severe neonatal-onset encephalopathy with microcephaly", "ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS", "Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations", "encephalopathy, neonatal severe, due to MECP2 mutations", "Methyl-cytosine phosphate guanine binding protein 2 related severe neonatal encephalopathy", "Methyl-cytosine phosphate guanine binding protein 2 related severe neonatal encephalopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe neonatal-onset encephalopathy with microcephaly", "shortest_name_length": 44}
{"curie": "MONDO:0021496", "names": ["Benign Lip Tumor", "benign Lip tumor", "Benign lip neoplasm", "Benign tumor of lip", "Benign Tumor of Lip", "Benign Lip Neoplasm", "lip neoplasm benign", "benign Lip neoplasm", "benign tumor of Lip", "Lip neoplasm benign", "lip benign neoplasm", "Lip Neoplasm, Benign", "lip neoplasm, benign", "Benign tumour of lip", "Benign neoplasm of lip", "benign neoplasm of lip", "Benign Neoplasm of Lip", "Benign Tumor of the Lip", "benign tumor of the Lip", "Benign Neoplasm of the Lip", "benign neoplasm of the Lip", "Benign neoplasm of the lip", "Benign neoplasm of lip, NOS", "Benign neoplasm of lip (disorder)", "benign neoplasm of lip (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of lip", "shortest_name_length": 16}
{"curie": "MONDO:0000158", "names": ["CDH", "DDH", "Hip dysplasia", "ACETABULAR DYSPLASIA", "acetabulum dysplasia", "acetabulum; dysplasia", "dysplasia; acetabulum", "dysplasia of acetabulum", "Dysplasia of acetabulum", "HIP DYSPLASIA CONGENITAL", "congenital dysplasia hip", "congenital hip dysplasia", "Congenital Hip Dysplasia", "Congenital hip dysplasia", "Hip Dysplasia, Congenital", "Congenital Hip Dysplasias", "HIP DYSPLASIA, CONGENITAL", "Dysplasia, Congenital Hip", "hip congenital dislocation", "Hip Dysplasias, Congenital", "congenital dislocation hip", "congenital hip dislocation", "Dysplasias, Congenital Hip", "Congenital Hip Dislocation", "Congenital Hip Dislocations", "congenital hip dislocations", "Congenital Hip Displacement", "Hip Dislocation, Congenital", "Developmental hip dysplasia", "congenital dislocation hips", "Dislocation, Congenital Hip", "Developmental Hip Dysplasia", "HIP DYSPLASIA, DEVELOPMENTAL", "Displacement, Congenital Hip", "Dislocations, Congenital Hip", "Hip Displacement, Congenital", "Congenital Hip Displacements", "Developmental Hip Dysplasias", "Dysplasia, Developmental Hip", "Hip Dysplasia, Developmental", "Hip Dislocations, Congenital", "Displacements, Congenital Hip", "developmental dislocation hip", "congenital dislocation of hip", "Developmental Hip Dislocation", "Hip Displacements, Congenital", "Abnormal formation of the hip", "developmental hip dislocation", "Congenital Dislocation of Hip", "developmental dislocation hips", "Dislocation, Developmental Hip", "Developmental Dysplasia of Hip", "Developmental Hip Dislocations", "Hip Dislocation, Developmental", "Dislocation Of Hip, Congenital", "developmental dysplasia of hip", "developmental hip displacement", "congenital dysplasia of the hip", "Congenital dysplasia of the hip", "Congenital Dysplasia Of The Hip", "Hip, Dislocation Of, Congenital", "Congenital acetabular dysplasia", "congenital acetabular dysplasia", "Developmental Dislocation of Hip", "developmental dislocation of hip", "Developmental Dysplasia of the Hip", "Developmental dysplasia of the hip", "developmental dysplasia of the hip", "Congenital hip dysplasia (disorder)", "DDH - developmental dysplasia of hip", "congenital hip dysplasia (diagnosis)", "developmental dysplasia of hip (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental dysplasia of the hip", "shortest_name_length": 3}
{"curie": "MONDO:0006130", "names": ["CNS tumor", "CNS Tumor", "CNS Neoplasm", "Tumor of CNS", "tumor of CNS", "CNS neoplasm", "neoplasm of CNS", "Neoplasm of CNS", "tumor of the CNS", "Tumor of the CNS", "Brain/Spinal Cord Tumor", "brain/spinal cord tumor", "Central Nervous System Tumor", "central nervous system tumor", "tumor of central nervous system", "Central Nervous System Neoplasm", "Tumor of Central Nervous System", "central nervous system neoplasm", "neoplasm of central nervous system", "Neoplasm of Central Nervous System", "Tumor of the Central Nervous System", "tumor of the central nervous system", "Neoplasm of the Central Nervous System", "neoplasm of the central nervous system", "central nervous system neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system neoplasm", "shortest_name_length": 9}
{"curie": "MONDO:0001137", "names": ["MVE", "mve", "Australian X disease", "Australian; X disease", "X disease; Australian", "Australian X; disease", "Encephalitis australia", "australia encephalitis", "Australian encephalitis", "Australian; encephalitis", "encephalitis; Australian", "Murray River encephalitis", "Murray Valley encephalitis", "Murray Valley-encephalitis", "murray valley encephalitis", "Murray valley encephalitis", "encephalitis; Murray Valley", "Australian arboencephalitis", "Australian; arboencephalitis", "arboencephalitis; Australian", "MVE - Murray Valley encephalitis", "Murray valley encephalitis (MVE)", "Australian encephalitis (diagnosis)", "disease (or disorder); Australian X", "Murray Valley encephalitis (disorder)", "Murray Valley encephalitis (diagnosis)", "Murray Valley encephalitis virus infectious disease", "Murray Valley encephalitis virus disease or disorder", "Murray Valley encephalitis virus caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Murray valley encephalitis", "shortest_name_length": 3}
{"curie": "MONDO:0010135", "names": ["TDH3", "GDTH III", "Iodotyrosyl coupling defect", "Thyroid Dyshormonogenesis 3", "thyroid dyshormonogenesis 3", "THYROID DYSHORMONOGENESIS 3", "Thyroid hormone coupling defect", "thyroid dyshormonogenesis type 3", "TG familial thyroid dyshormonogenesis", "Hypothyroidism due to coupling defect", "Iodotyrosyl coupling defect (disorder)", "Congenital thyroid hormone coupling defect", "genetic defect in thyroid hormonogenesis 3", "Genetic defect in thyroid hormonogenesis III", "THYROID HORMONOGENESIS, GENETIC DEFECT IN, 3", "thyroid hormonogenesis, genetic defect in, 3", "Thyroid Hormonogenesis, Genetic Defect in, 3", "Hypothyroidism, Congenital, due to Dyshormonogenesis, 3", "hypothyroidism, congenital, due to dyshormonogenesis, 3", "HYPOTHYROIDISM, CONGENITAL, DUE TO DYSHORMONOGENESIS, 3", "GDTH III - genetic defect in thyroid hormonogenesis III", "familial thyroid dyshormonogenesis caused by mutation in TG"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid dyshormonogenesis 3", "shortest_name_length": 4}
{"curie": "UMLS:C0278530", "names": ["relapsed adult HD", "adult HD, relapsed", "recurrent adult HD", "adult HD, recurrent", "recurrent HD, adult", "HD, relapsed, adult", "HD, adult, relapsed", "HD, adult, recurrent", "HD, recurrent, adult", "Recurrent Hodgkin Lymphoma", "Relapsed Adult Hodgkin's Disease", "Recurrent Adult Hodgkin Lymphoma", "recurrent adult Hodgkin lymphoma", "relapsed adult Hodgkin's disease", "recurrent adult Hodgkin's disease", "Recurrent Adult Hodgkin's Disease", "relapsed Hodgkin's disease, adult", "Relapsed Adult Hodgkin's Lymphoma", "adult Hodgkin's disease, relapsed", "recurrent Hodgkin's disease, adult", "adult Hodgkin's disease, recurrent", "lymphoma, relapsed adult Hodgkin's", "Hodgkin's disease, relapsed, adult", "Recurrent Adult Hodgkin's Lymphoma", "Hodgkin's lymphoma, relapsed, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Adult Hodgkin Lymphoma", "shortest_name_length": 17}
{"curie": "MONDO:0017205", "names": ["primary oculocerebral lymphoma", "primary oculocerebral non-Hodgkin lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary oculocerebral lymphoma", "shortest_name_length": 30}
{"curie": "UMLS:C4724990", "names": ["Refractory Hypopharyngeal Squamous Cell Carcinoma", "Refractory Hypopharyngeal Throat Squamous Cell Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Hypopharyngeal Squamous Cell Carcinoma", "shortest_name_length": 49}
{"curie": "MONDO:0000314", "names": ["primary bacterial infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary bacterial infectious disease", "shortest_name_length": 36}
{"curie": "MONDO:0016806", "names": ["mtDNA-related dystonia", "Mitochondrial DNA-related dystonia", "Maternally-inherited mitochondrial dystonia", "Maternally inherited mitochondrial dystonia", "maternally-inherited mitochondrial dystonia", "Maternally inherited mitochondrial dystonia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maternally-inherited mitochondrial dystonia", "shortest_name_length": 22}
{"curie": "MONDO:0015043", "names": ["extramedullary soft tissue plasmacytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extramedullary soft tissue plasmacytoma", "shortest_name_length": 39}
{"curie": "MONDO:0013112", "names": ["BESC3", "Besc3", "bronchiectasis 3", "SCNN1G bronchiectasis", "cystic fibrosis-like syndrome", "CYSTIC FIBROSIS-LIKE SYNDROME", "bronchiectasis caused by mutation in SCNN1G", "bronchiectasis with or without elevated sweat chloride 3", "Bronchiectasis With Or Without Elevated Sweat Chloride 3", "BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 3", "bronchiectasis with or without elevated sweat chloride type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bronchiectasis with or without elevated sweat chloride 3", "shortest_name_length": 5}
{"curie": "MONDO:0012378", "names": ["HGF3", "GGF3", "GINGF3", "gingival fibromatosis, 3", "fibromatosis, gingival, 3", "FIBROMATOSIS, GINGIVAL, 3", "Fibromatosis, gingival, 3", "hereditary gingival fibromatosis, 3", "fibromatosis gingival, hereditary, 3", "Fibromatosis, gingival, hereditary, 3", "FIBROMATOSIS, GINGIVAL, HEREDITARY, 3", "fibromatosis, gingival, hereditary, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibromatosis, gingival, 3", "shortest_name_length": 4}
{"curie": "MONDO:0015500", "names": ["facial arteriovenous malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "facial arteriovenous malformation", "shortest_name_length": 33}
{"curie": "MONDO:0008771", "names": ["ERS", "ers", "AI1G", "AIGFS", "Enamel renal syndrome", "enamel renal syndrome", "Enamel-Renal Syndrome", "Enamel-renal syndrome", "ENAMEL-RENAL SYNDROME", "enamel-renal syndrome", "McGibbon Lubinsky syndrome", "ENAMEL-RENAL-GINGIVAL SYNDROME", "enamel-renal-gingival syndrome", "FAM20A amelogenesis imperfecta", "amelogenesis imperfecta type 1G", "amelogenesis imperfecta type IG", "Amelogenesis Imperfecta, Type IG", "Enamel-renal syndrome (disorder)", "amelogenesis imperfecta, type IG", "AMELOGENESIS IMPERFECTA, TYPE IG", "amelogenesis imperfecta nephrocalcinosis", "Amelogenesis imperfecta nephrocalcinosis", "amelogenesis imperfecta hypoplastic type, IG", "Amelogenesis imperfecta and nephrocalcinosis", "amelogenesis imperfecta and nephrocalcinosis", "Amelogenesis imperfecta-nephrocalcinosis syndrome", "amelogenesis imperfecta-nephrocalcinosis syndrome", "generalized enamel hypoplasia and renal dysfunction", "Generalized enamel hypoplasia and renal dysfunction", "amelogenesis imperfecta caused by mutation in FAM20A", "amelogenesis imperfecta-gingival hyperplasia syndrome", "amelogenesis imperfecta, type IG (enamel-renal syndrome)", "amelogenesis imperfecta hypoplastic with nephrocalcinosis", "AMELOGENESIS IMPERFECTA AND GINGIVAL FIBROMATOSIS SYNDROME", "Amelogenesis Imperfecta, Hypoplastic, and Nephrocalcinosis", "amelogenesis imperfecta and gingival fibromatosis syndrome", "AMELOGENESIS IMPERFECTA, HYPOPLASTIC, WITH NEPHROCALCINOSIS", "amelogenesis imperfecta, hypoplastic, with nephrocalcinosis", "absent enamel, nephrocalcinosis and apparently normal calcium metabolism", "Absent enamel, nephrocalcinosis and apparently normal calcium metabolism", "Amelogenesis imperfecta, nephrocalcinosis and impaired renal concentration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amelogenesis imperfecta type 1G", "shortest_name_length": 3}
{"curie": "UMLS:C0278592", "names": ["Angiosarcoma", "adult angiosarcoma", "Adult Angiosarcoma", "angiosarcoma, adult", "adult, angiosarcoma", "adult hemangiosarcoma", "Adult Hemangiosarcoma", "hemangiosarcoma, adult", "sarcoma, angio-, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Angiosarcoma", "shortest_name_length": 12}
{"curie": "MONDO:0008453", "names": ["SMAFK", "Finkel disease", "Finkel Late-Adult Type SMA", "FINKEL LATE-ADULT TYPE SMA", "Finkel late-adult type SMA", "Finkel late-adult type Sma", "autosomal dominant adult-onset proximal SMA", "SMAFK - spinal muscular atrophy Finkel type", "Autosomal dominant adult-onset proximal SMA", "Spinal Muscular Atrophy, Late-Onset, Finkel Type", "SPINAL MUSCULAR ATROPHY, LATE-ONSET, FINKEL TYPE", "spinal muscular atrophy, late-onset, FINKEL type", "autosomal dominant adult proximal spinal muscular atrophy", "spinal muscular atrophy, proximal, adult, autosomal dominant", "Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant", "SPINAL MUSCULAR ATROPHY, PROXIMAL, ADULT, AUTOSOMAL DOMINANT", "Autosomal dominant adult-onset proximal spinal muscular atrophy", "autosomal dominant adult-onset proximal spinal muscular atrophy", "adult-onset proximal spinal muscular atrophy, autosomal dominant", "Autosomal dominant late-onset spinal muscular atrophy Finkel type", "Autosomal dominant late-onset spinal muscular atrophy, Finkel type", "autosomal dominant late-onset spinal muscular atrophy, Finkel type", "Autosomal dominant adult-onset proximal spinal muscular atrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult-onset proximal spinal muscular atrophy, autosomal dominant", "shortest_name_length": 5}
{"curie": "MONDO:0001766", "names": ["eversion of lacrimal punctum", "Eversion of lacrimal punctum", "Eversion of lacrimal punctum (disorder)", "eversion of lacrimal punctum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eversion of lacrimal punctum", "shortest_name_length": 28}
{"curie": "UMLS:C5670182", "names": ["Metastatic Triple-Negative Breast Inflammatory Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Triple-Negative Breast Inflammatory Carcinoma", "shortest_name_length": 56}
{"curie": "MONDO:0018182", "names": ["Impetigo bullosa", "impetigo bullosa", "bullous impetigo", "Bullous impetigo", "impetigo bullous", "IMPETIGO BULLOUS", "Impetigo, bullous", "bullous; impetigo", "impetigo; bullosa", "Impetigo contagiosa bullosa", "Impetigo bullosa (disorder)", "bullous impetigo (diagnosis)", "Impetigo contagiosa, bullous", "Bullous staphylococcal impetigo", "impetigo bullous staphylococcal", "bullous staphylococcal impetigo", "bullous staphylococcal impetigo (diagnosis)", "Impetigo contagiosa of any site and any organism, bullous"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bullous impetigo", "shortest_name_length": 16}
{"curie": "UMLS:C0948588", "names": ["Lymphangiosis carcinomatosa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphangiosis carcinomatosa", "shortest_name_length": 27}
{"curie": "MONDO:0030841", "names": ["MMRCS3", "mismatch repair cancer syndrome 3", "MISMATCH REPAIR CANCER SYNDROME 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mismatch repair cancer syndrome 3", "shortest_name_length": 6}
{"curie": "MONDO:0010982", "names": ["Ichthyosis-Mental Retardation Syndrome with Large Keratohyalin Granules in the Skin", "ICHTHYOSIS-MENTAL RETARDATION SYNDROME WITH LARGE KERATOHYALIN GRANULES IN THE SKIN", "ichthyosis-mental retardation syndrome with large keratohyalin granules in the skin", "ichthyosis-intellectual disability syndrome with large keratohyalin granules in the skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ichthyosis-intellectual disability syndrome with large keratohyalin granules in the skin", "shortest_name_length": 83}
{"curie": "UMLS:C1708903", "names": ["Malignant Pilar Tumor", "Malignant Proliferating Pilar Tumor", "Malignant Proliferating Trichilemmal Cyst", "Malignant Proliferating Trichilemmal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Proliferating Pilar Tumor", "shortest_name_length": 21}
{"curie": "MONDO:0004406", "names": ["central nervous system Mixed germ cell tumor", "Central Nervous System Mixed Germ Cell Tumor", "adult central nervous system mixed germ cell tumor", "Adult Central Nervous System Mixed Germ Cell Tumor", "adult mixed germ cell tumor of central nervous system", "mixed germ cell tumor of central nervous system of adults"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult central nervous system mixed germ cell tumor", "shortest_name_length": 44}
{"curie": "UMLS:C1698629", "names": ["Duodenal infection", "Duodenal Infection", "Duodenal infection (diagnosis)", "small intestine infection duodenum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Duodenal Infection", "shortest_name_length": 18}
{"curie": "MONDO:0016614", "names": ["mild peroxismal disorder due to PEX10 deficiency", "autosomal recessive ataxia due to PEX10 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive ataxia due to PEX10 deficiency", "shortest_name_length": 48}
{"curie": "UMLS:C3899155", "names": ["Familial Neuroblastoma", "Hereditary Neuroblastoma", "hereditary neuroblastoma", "neuroblastoma, hereditary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Familial Neuroblastoma", "shortest_name_length": 22}
{"curie": "UMLS:C0302497", "names": ["Retrobulbar hematoma", "Retrobulbar haematoma", "Retrobulbar hemorrhage", "retrobulbar hemorrhage", "Retrobulbar Hemorrhage", "retrobulbar haemorrhage", "Retrobulbar Hemorrhages", "Retrobulbar haemorrhage", "Hemorrhage, Retrobulbar", "Retrobulbar hemorrhage (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retrobulbar Hemorrhage", "shortest_name_length": 20}
{"curie": "UMLS:C1167661", "names": ["Cerebral vasoconstriction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebral vasoconstriction", "shortest_name_length": 25}
{"curie": "UMLS:C4724992", "names": ["Refractory Oral Cavity Squamous Cell Cancer", "Refractory Oral Cavity Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Oral Cavity Squamous Cell Carcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0019669", "names": ["HYPOCHONDROGENESIS", "hypochondrogenesis", "Hypochondrogenesis", "Hypochondrogenesis (disorder)", "Hypochondrogenesis (diagnosis)", "spondylodysplastic dysplasias hypochondrogenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypochondrogenesis", "shortest_name_length": 18}
{"curie": "MONDO:0010678", "names": ["muscular dystrophy, progressive Pectorodorsal", "Muscular Dystrophy, Progressive Pectorodorsal", "MUSCULAR DYSTROPHY, PROGRESSIVE PECTORODORSAL", "MUSCULAR DYSTROPHY, PROGRESSIVE, INVOLVING SHOULDER GIRDLE AND BACK", "Muscular Dystrophy, Progressive, Involving Shoulder Girdle and Back", "muscular dystrophy, progressive, involving shoulder girdle and back"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy, progressive Pectorodorsal", "shortest_name_length": 45}
{"curie": "MONDO:0015694", "names": ["mucosa melanoma", "mucosa melanoma (disease)", "melanoma (disease) of mucosa", "malignant melanoma of the mucosa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant melanoma of the mucosa", "shortest_name_length": 15}
{"curie": "MONDO:0100340", "names": ["FA1", "FARR", "FRDA1", "Frda1", "Friedreich ataxia", "FRIEDREICH ATAXIA 1", "Friedreich ataxia 1", "Friedreich Ataxia 1", "Friedreich ataxia type 1", "Friedreich Ataxia with Retained Reflexes", "FRIEDREICH ATAXIA WITH RETAINED REFLEXES", "Friedreich ataxia with retained reflexes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Friedreich ataxia 1", "shortest_name_length": 3}
{"curie": "MONDO:0004162", "names": ["Uterine Corpus Cellular Leiomyoma", "uterine corpus cellular leiomyoma", "body of uterus cellular leiomyoma", "cellular leiomyoma of body of uterus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine corpus cellular leiomyoma", "shortest_name_length": 33}
{"curie": "MONDO:0009357", "names": ["Humeroradial Synostosis with Craniofacial Anomalies", "HUMERORADIAL SYNOSTOSIS WITH CRANIOFACIAL ANOMALIES", "humeroradial synostosis with craniofacial anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "humeroradial synostosis with craniofacial anomalies", "shortest_name_length": 51}
{"curie": "MONDO:0005417", "names": ["wet AMD", "wet ARMD", "Kuhnt-Junius", "Wet Macular Degeneration", "wet macular degeneration", "Wet macular degeneration", "Kuhnt-Junius degeneration", "Wet Macular Degenerations", "Junius-Kuhnt degeneration", "Degeneration, Wet Macular", "Macular Degeneration, Wet", "Macular Degenerations, Wet", "Degenerations, Wet Macular", "Kuhnt-Junius; degeneration", "degeneration; Kuhnt-Junius", "exudative macular degeneration", "Disciform macular degeneration", "macular degeneration exudative", "disciform macular degeneration", "Wet senile macular degeneration", "wet senile macular degeneration", "exudative degeneration of macula", "Senile macular degeneration, wet", "Kuhnt-Junius macular degeneration", "retina; degeneration, Kuhnt-Junius", "degeneration; retina, Kuhnt-Junius", "wet exudative macular degeneration", "EMD - Exudative macular degeneration", "wet age related macular degeneration", "Exudative senile macular degeneration", "Subretinal neovascularization of macula", "wet senile macular retinal degeneration", "Wet senile macular retinal degeneration", "Subretinal neovascularisation of macula", "disciform exudative macular degeneration", "exudative macular degeneration (diagnosis)", "Exudative age-related macular degeneration", "Neovascular age-related macular degeneration", "neovascular age-related macular degeneration", "Kuhnt-Junius macular degeneration (diagnosis)", "Exudative senile macular retinal degeneration", "Disciform senile macular retinal degeneration", "wet exudative macular degeneration (diagnosis)", "exudative senile macular degeneration of retina", "Exudative senile macular degeneration of retina", "exudative degeneration of macula (physical finding)", "disciform exudative macular degeneration (diagnosis)", "Exudative age-related macular degeneration (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "wet macular degeneration", "shortest_name_length": 7}
{"curie": "UMLS:C1697749", "names": ["Cranial nerve infection", "infection cranial nerve", "Cranial Nerve Infection", "Infection of cranial nerve", "Cranial nerve infection (diagnosis)", "Infection of cranial nerve (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cranial Nerve Infection", "shortest_name_length": 23}
{"curie": "MONDO:0001405", "names": ["Hebrae", "Jock itch", "Jock Itch", "jock itch", "dhobi itch", "Jock Itchs", "itch; jock", "Dhobi itch", "jock; itch", "dhobie itch", "dhobi; itch", "Dhobie itch", "Groin tinea", "itch; dhobi", "groin tinea", "TINEA CRURIS", "jock itching", "Itching;jock", "itching jock", "tinea cruris", "Tinea cruris", "cruris; tinea", "tinea; cruris", "Tinea of groin", "Groin ringworm", "groin ringworm", "ringworm; groin", "groin; ringworm", "tinea inguinalis", "Tinea inguinalis", "Eczema marginatum", "Ringworm of groin", "eczema; marginatum", "marginatum; eczema", "Ringworm of scrotum", "Tinea cruris (disorder)", "tinea cruris (diagnosis)", "dermatophytosis of groin & perianal area", "Dermatophytosis of groin & perianal area", "Dermatophytosis of groin and perianal area", "dermatophytosis of groin and perianal area", "Dermatophytosis of Groin and Perianal Area"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermatophytosis of groin and perianal area", "shortest_name_length": 6}
{"curie": "UMLS:C5556496", "names": ["High Grade Urothelial Carcinoma", "High-Grade Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Urothelial Carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0008829", "names": ["chylous ascites", "Chyloperitoneum", "chyloperitoneum", "Chylous Ascites", "Chylous ascites", "ascites chylous", "CHYLOUS ASCITES", "Ascites chylous", "ascites, chylous", "chylous; ascites", "Ascites, Chylous", "ascites; chylous", "ASCITES, CHYLOUS", "CHYLOUS PERITONEAL FLUID", "congenital chylous ascites", "Chylous ascites (disorder)", "chylous ascites (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chylous ascites", "shortest_name_length": 15}
{"curie": "MONDO:0043923", "names": ["Oral Lichen Planus", "lichen planus oral", "oral lichen planus", "Oral lichen planus", "lichen oral planus", "Lichen Planus, Oral", "lichen planus, oral", "olp - oral lichen planus", "OLP - Oral lichen planus", "Oral lichen planus (disorder)", "oral lichen planus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lichen planus, oral", "shortest_name_length": 18}
{"curie": "MONDO:0009598", "names": ["RPSKA", "METAPHYSEAL CHONDRODYSPLASIA WITH RETINITIS PIGMENTOSA", "Metaphyseal Chondrodysplasia with Retinitis Pigmentosa", "metaphyseal chondrodysplasia with retinitis pigmentosa", "RETINITIS PIGMENTOSA WITH OR WITHOUT SKELETAL ANOMALIES", "retinitis pigmentosa with or without skeletal anomalies", "brachydactyly-short stature-retinitis pigmentosa syndrome", "metaphyseal chondrodysplasia-retinitis pigmentosa syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metaphyseal chondrodysplasia-retinitis pigmentosa syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0700018", "names": ["chromosome 11 disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 11 disorder", "shortest_name_length": 22}
{"curie": "MONDO:0017105", "names": ["glioependymal/ependymal cyst"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glioependymal/ependymal cyst", "shortest_name_length": 28}
{"curie": "MONDO:0012375", "names": ["DFNB47", "autosomal recessive deafness 47", "deafness, autosomal recessive 47", "Deafness, Autosomal Recessive 47", "DEAFNESS, AUTOSOMAL RECESSIVE 47", "autosomal recessive nonsyndromic deafness 47", "deafness, neurosensory, autosomal recessive 47", "autosomal recessive nonsyndromic hearing loss 47", "autosomal recessive nonsyndromic deafness type 47"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 47", "shortest_name_length": 6}
{"curie": "UMLS:C5237383", "names": ["Locally Advanced Hypopharyngeal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Hypopharyngeal Squamous Cell Carcinoma", "shortest_name_length": 55}
{"curie": "MONDO:0013327", "names": ["HP3", "PH III", "HOGA1 primary hyperoxaluria", "primary hyperoxaluria type 3", "Primary hyperoxaluria type 3", "Primary hyperoxaluria type III", "hyperoxaluria, primary, type 3", "Primary Hyperoxaluria Type III", "primary hyperoxaluria type III", "HYPEROXALURIA, PRIMARY, TYPE III", "hyperoxaluria, primary, type III", "Primary hyperoxaluria type III (disorder)", "primary hyperoxaluria caused by mutation in HOGA1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary hyperoxaluria type 3", "shortest_name_length": 3}
{"curie": "UMLS:C3272526", "names": ["Small Intestinal Kaposi Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Intestinal Kaposi Sarcoma", "shortest_name_length": 31}
{"curie": "MONDO:0800124", "names": ["Lane Hamilton syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lane Hamilton syndrome", "shortest_name_length": 22}
{"curie": "MONDO:0008411", "names": ["ums", "UMS", "Schinzel syndrome", "SCHINZEL SYNDROME", "ulnar-mammary syndrome", "ULNAR-MAMMARY SYNDROME", "Ulnar-mammary syndrome", "Ulnar mammary syndrome", "Pallister ulnar-mammary syndrome", "PALLISTER ULNAR-MAMMARY SYNDROME", "Ulnar mammary syndrome (disorder)", "Ulnar-mammary syndrome of Pallister", "ulnar-mammary syndrome of Pallister"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ulnar-mammary syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C1400301", "names": ["nOH", "Neurogenic Orthostatic Hypotension", "Neurogenic orthostatic hypotension", "orthostatic; hypotension, neurogenic", "hypotension; orthostatic, neurogenic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neurogenic Orthostatic Hypotension", "shortest_name_length": 3}
{"curie": "MONDO:0007533", "names": ["EL2", "ELLIPTOCYTOSIS 2", "elliptocytosis 2", "elliptocytosis-2", "Elliptocytosis 2", "elliptocytosis type 2", "SPTA1 hereditary elliptocytosis", "ELLIPTOCYTOSIS, RHESUS-UNLINKED TYPE", "Elliptocytosis, Rhesus-Unlinked Type", "elliptocytosis, Rhesus-unlinked type", "hereditary elliptocytosis caused by mutation in SPTA1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "elliptocytosis 2", "shortest_name_length": 3}
{"curie": "MONDO:0020357", "names": ["lid coloboma", "Lid coloboma", "Cleft eyelid", "Notched eyelid", "Coloboma of lid", "Eyelid coloboma", "Notched eyelids", "eyelid coloboma", "Eyelid colobomas", "coloboma; eyelid", "eyelid; coloboma", "Eyelid colobomata", "coloboma palpebral", "Palpebral coloboma", "Coloboma of eyelid", "coloboma of eyelid", "Coloboma of Eyelid", "Coloboma palpebrale", "coloboma of the eyelid", "Coloboma of the Eyelid", "congenital eyelid coloboma", "Coloboma of eyelid (disorder)", "Full thickness defect of the eyelid", "coloboma palpebral (physical finding)", "congenital eyelid coloboma (diagnosis)", "Congenital notching of palpebral fissure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coloboma of eyelid", "shortest_name_length": 12}
{"curie": "UMLS:C0009792", "names": ["Consciousness Disorder", "Consciousness Disorders", "Disorder of Consciousness", "disorders of consciousness", "Disorders of Consciousness", "disorders of consciousness (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Consciousness Disorders", "shortest_name_length": 22}
{"curie": "MONDO:0003105", "names": ["Prostate Disease", "disease prostate", "Prostate disease", "prostate disease", "Disease;prostate", "diseases prostate", "Prostatic Disease", "prostate diseases", "PROSTATE DISORDER", "prostatic disease", "Prostate Disorder", "disease prostates", "Prostate Diseases", "prostate disorder", "Prostate--Diseases", "Disease, Prostatic", "PROSTATIC DISORDER", "disorders prostate", "prostatic diseases", "Prostatic Diseases", "prostate disorders", "Prostatic disorder", "of prostate disease", "Diseases, Prostatic", "Disorder of prostate", "prostate gland disease", "Prostatic disorder NOS", "Prostatic disorder, NOS", "DISEASES OF THE PROSTATE", "Disease of prostate, NOS", "Disorder of prostate, NOS", "disease of prostate gland", "disorder of prostate gland", "Prostatic disease or syndrome", "prostate disorders (diagnosis)", "Disorder of prostate (disorder)", "disease (or disorder); prostate", "Prostatic Diseases and Syndromes", "Unspecified disorder of prostate", "Disorder of prostate, unspecified", "prostate gland disease or disorder", "disease or disorder of prostate gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate disorder", "shortest_name_length": 16}
{"curie": "UMLS:C1858586", "names": ["Mild anemia", "Mild Anemia", "Anemia, mild", "Anemia (mild)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anemia (mild)", "shortest_name_length": 11}
{"curie": "UMLS:C0877173", "names": ["food aversion", "Food aversion", "aversion food", "aversions food"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Food aversion", "shortest_name_length": 13}
{"curie": "MONDO:0015942", "names": ["FMD", "Frontometaphyseal dysplasia", "frontometaphyseal dysplasia", "FMD - Frontometaphyseal dysplasia", "Frontometaphyseal dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontometaphyseal dysplasia", "shortest_name_length": 3}
{"curie": "MONDO:0013233", "names": ["HJD", "Hjd", "HANDIGODU JOINT DISEASE", "Handigodu JOINT disease", "Spondyloepimetaphyseal dysplasia Handigodu type", "SPONDYLOEPIMETAPHYSEAL DYSPLASIA, HANDIGODU TYPE", "Spondyloepimetaphyseal dysplasia, Handigodu type", "spondyloepimetaphyseal dysplasia, Handigodu type", "Spondyloepimetaphyseal dysplasia Handigodu type (disorder)", "Spondyloepimetaphyseal dysplasia Handigodu type (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepimetaphyseal dysplasia, Handigodu type", "shortest_name_length": 3}
{"curie": "MONDO:0017673", "names": ["isolated focal PPK", "isolated focal palmoplantar keratoderma", "isolated focal keratosis palmoplantaris", "isolated focal palmoplantar hyperkeratosis", "nonsyndromic focal palmoplantar keratoderma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated focal palmoplantar keratoderma", "shortest_name_length": 18}
{"curie": "MONDO:0000114", "names": ["cerebelloparenchymal disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebelloparenchymal disorder", "shortest_name_length": 29}
{"curie": "MONDO:0020360", "names": ["complete cryptophthalmia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complete cryptophthalmia", "shortest_name_length": 24}
{"curie": "UMLS:C5420082", "names": ["Malignant Sinonasal Soft Tissue Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Sinonasal Soft Tissue Neoplasm", "shortest_name_length": 40}
{"curie": "MONDO:0015470", "names": ["familial isolated dilated cardiomyopathy", "familial or idiopathic dilated cardiomyopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial isolated dilated cardiomyopathy", "shortest_name_length": 40}
{"curie": "MONDO:0002797", "names": ["Medulloblastoma", "medulloblastoma", "Childhood Medulloblastoma", "childhood cerebellar PNET", "Pediatric Medulloblastoma", "childhood medulloblastoma", "pediatric medulloblastoma", "pediatric cerebellar PNET", "pediatric Medulloblastoma", "medulloblastoma, pediatric", "PNET, childhood cerebellar", "PNET, pediatric cerebellar", "cerebellar PNET, pediatric", "cerebellar PNET, childhood", "Medulloblastoma, Childhood", "medulloblastoma, childhood", "Childhood Medulloblastomas", "PNET, cerebellar, pediatric", "cerebellar, pediatric, PNET", "Medulloblastomas, Childhood", "PNET, cerebellar, childhood", "cerebellar, childhood, PNET", "medulloblastoma of childhood", "childhood infratentorial PNET", "pediatric infratentorial PNET", "infratentorial PNET, pediatric", "PNET, childhood infratentorial", "infratentorial PNET, childhood", "PNET, pediatric infratentorial", "infratentorial, pediatric, PNET", "infratentorial, childhood, PNET", "PNET, infratentorial, pediatric", "PNET, infratentorial, childhood", "Brain tumor, child: Medulloblastoma", "pediatric cerebellar primitive neuroectodermal tumor", "childhood cerebellar primitive neuroectodermal tumor", "primitive neuroectodermal tumor, childhood cerebellar", "primitive neuroectodermal tumor, pediatric cerebellar", "cerebellar primitive neuroectodermal tumor, childhood", "cerebellar primitive neuroectodermal tumor, pediatric", "childhood infratentorial primitive neuroectodermal tumor", "pediatric infratentorial primitive neuroectodermal tumor", "primitive neuroectodermal tumor, pediatric infratentorial", "infratentorial primitive neuroectodermal tumor, pediatric", "infratentorial primitive neuroectodermal tumor, childhood", "primitive neuroectodermal tumor, childhood infratentorial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood medulloblastoma", "shortest_name_length": 15}
{"curie": "UMLS:C1336486", "names": ["Stage I Supradiaphragmatic Hodgkin Lymphoma", "Stage I Supradiaphragmatic Hodgkin's Disease", "Stage I Hodgkin's Disease above the Diaphragm", "Stage I Supradiaphragmatic Hodgkin's Lymphoma", "Stage I Hodgkin's Lymphoma above the Diaphragm", "Ann Arbor Stage I Supradiaphragmatic Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage I Supradiaphragmatic Hodgkin Lymphoma", "shortest_name_length": 43}
{"curie": "MONDO:0016372", "names": ["Weesenberg's syndrome", "Glossopharyngeal neuralgia", "neuralgia glossopharyngeal", "glossopharyngeal neuralgia", "Glossopharyngeal Neuralgia", "glossopharyngeal; neuralgia", "Glossopharyngeal Neuralgias", "neuralgia; glossopharyngeal", "Neuralgia, Glossopharyngeal", "NEURALGIA, GLOSSOPHARYNGEAL", "Neuralgias, Glossopharyngeal", "Glossovasopharyngeal neuralgia", "glossopharyngeal nerve neuralgia", "neuralgia of glossopharyngeal nerve", "Glossopharyngeal neuralgia syndrome", "Glossopharyngeal neuralgia (finding)", "glossopharyngeal neuralgia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glossopharyngeal neuralgia", "shortest_name_length": 21}
{"curie": "MONDO:0003771", "names": ["jugular foramen meningioma", "Jugular Foramen Meningioma", "meningioma of jugular Foramen", "Meningioma of Jugular Foramen", "meningioma of the jugular Foramen", "meningioma of the Jugular Foramen", "Meningioma of the Jugular Foramen", "jugular foramen meningioma (disease)", "meningioma (disease) of jugular foramen"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "jugular foramen meningioma", "shortest_name_length": 26}
{"curie": "MONDO:0004082", "names": ["pediatric ovarian immature teratoma", "Childhood Ovarian Immature Teratoma", "childhood ovarian immature teratoma", "pediatric immature ovarian teratoma", "childhood immature ovarian teratoma", "Pediatric Ovarian Immature Teratoma", "Childhood Immature Teratoma of Ovary", "pediatric immature teratoma of ovary", "childhood immature teratoma of ovary", "Pediatric Immature Teratoma of Ovary", "pediatric Immature teratoma of Ovary", "immature ovarian teratoma of childhood", "Pediatric Immature Teratoma of the Ovary", "Childhood Immature Teratoma of the Ovary", "pediatric immature teratoma of the ovary", "childhood immature teratoma of the ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood immature teratoma of ovary", "shortest_name_length": 35}
{"curie": "MONDO:0006988", "names": ["Sulfemoglobinemia", "sulfhemoglobinemia", "Sulfhemoglobinemia", "Sulphemoglobinemia", "SULFHEMOGLOBINEMIA", "Sulfhemoglobinemias", "Sulphaemoglobinaemia", "Sulfhaemoglobinaemia", "SULFHAEMOGLOBINAEMIA", "Sulfhemoglobinemia (disorder)", "sulfhemoglobinemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sulfhemoglobinemia", "shortest_name_length": 17}
{"curie": "MONDO:0001584", "names": ["Eye Movement Disorder", "Eye movement disorder", "eye movement disorder", "eye motility disorder", "Eye Motility Disorder", "Eye Movement Disorders", "Eye movement disorders", "eye motility disorders", "eye movement disorders", "Eye Motility Disorders", "Eye--Movement disorders", "ocular motility disease", "Ocular Motility Disorder", "disordered eye movements", "ocular motility disorder", "Disorder of eye movements", "Eye movement disorder NOS", "ocular motility disorders", "Ocular Motility Disorders", "disorder of eye movements", "DISORDERS OF EYE MOVEMENTS", "Disorder of eye movements, NOS", "Disorder of eye movements (disorder)", "ocular motility disorders (diagnosis)", "Unspecified disorder of eye movements"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ocular motility disease", "shortest_name_length": 21}
{"curie": "UMLS:C3275124", "names": ["Biliary Disease", "Biliary Disorder", "Biliary System Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Biliary System Disorder", "shortest_name_length": 15}
{"curie": "MONDO:0013524", "names": ["BDPLT13", "susceptibility to platelet-type bleeding disorder 13", "bleeding disorder, platelet-type, 13, susceptibility to", "bleeding diathesis due to thromboxane synthesis deficiency", "bleeding disorder, susceptibility to, due to defective platelet thromboxane A2 receptor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bleeding diathesis due to thromboxane synthesis deficiency", "shortest_name_length": 7}
{"curie": "UMLS:C1112423", "names": ["Post procedural bile leak"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post procedural bile leak", "shortest_name_length": 25}
{"curie": "MONDO:0000365", "names": ["GLC3C", "Congenital glaucoma", "Primary infantile glaucoma", "primary congenital glaucoma", "Primary Congenital Glaucoma", "Primary congenital glaucoma", "GLAUCOMA 3, PRIMARY CONGENITAL, C", "primary congenital glaucoma (disease)", "Primary congenital glaucoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary congenital glaucoma", "shortest_name_length": 5}
{"curie": "UMLS:C4763646", "names": ["Refractory Monomorphic Post-Transplant Lymphoproliferative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Monomorphic Post-Transplant Lymphoproliferative Disorder", "shortest_name_length": 67}
{"curie": "UMLS:C1282208", "names": ["preseptal cellulitis", "Preseptal Cellulitis", "cellulitis preseptal", "PRESEPTAL CELLULITIS", "Preseptal cellulitis", "Periorbital Cellulitis", "Preseptal cellulitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Preseptal cellulitis", "shortest_name_length": 20}
{"curie": "UMLS:C4764082", "names": ["Recurrent Transformed B-Cell Non-Hodgkin Lymphoma", "Recurrent Transformed Indolent B-Cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Transformed B-Cell Non-Hodgkin Lymphoma", "shortest_name_length": 49}
{"curie": "MONDO:0002383", "names": ["Pacinian tumor", "Pacinian tumour", "Pacinian neurofibroma", "Pacinian Neurofibroma", "Pacinian neurofibroma (disorder)", "Pacinian tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pacinian tumor", "shortest_name_length": 14}
{"curie": "UMLS:C5668441", "names": ["Refractory Indolent T-Cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Indolent T-Cell Non-Hodgkin Lymphoma", "shortest_name_length": 47}
{"curie": "MONDO:0016935", "names": ["Duplication of chromosome 17", "partial trisomy of chromosome 17", "Partial trisomy of chromosome 17", "Partial duplication of chromosome 17", "partial duplication of chromosome 17", "partial duplication of chromosome type 17", "Partial trisomy of chromosome 17 (disorder)", "partial trisomy of chromosome 17 (diagnosis)", "anomaly of chromosome pair 17 partial trisomy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of chromosome 17", "shortest_name_length": 28}
{"curie": "MONDO:0032877", "names": ["NEDBAS", "neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures", "NEURODEVELOPMENTAL DISORDER WITH NONSPECIFIC BRAIN ABNORMALITIES AND WITH OR WITHOUT SEIZURES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures", "shortest_name_length": 6}
{"curie": "MONDO:0020424", "names": ["intramural coronary arterial course"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intramural coronary arterial course", "shortest_name_length": 35}
{"curie": "UMLS:C1698676", "names": ["Vas deferens stenosis", "Vas Deferens Stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vas deferens stenosis", "shortest_name_length": 21}
{"curie": "UMLS:C4521607", "names": ["Stage I Pleural Malignant Mesothelioma", "Stage I Pleural Malignant Mesothelioma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Pleural Malignant Mesothelioma AJCC v8", "shortest_name_length": 38}
{"curie": "UMLS:C1336306", "names": ["Stage II Mouth Carcinoma", "Stage II Oral Cavity Cancer", "Stage II Carcinoma of Mouth", "Stage II Oral Cavity Carcinoma", "Stage II Carcinoma of the Mouth", "Stage II Carcinoma of Oral Cavity", "Stage II Oral Cavity Cancer AJCC v6", "Stage II Oral Cavity Cancer AJCC v7", "Stage II Carcinoma of the Oral Cavity", "Stage II Oral Cavity Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Oral Cavity Cancer AJCC v6 and v7", "shortest_name_length": 24}
{"curie": "MONDO:0000159", "names": ["bone marrow failure syndrome", "Bone Marrow Failure Syndrome", "Bone Marrow Failure Syndromes", "Bone Marrow Failure Disorders", "[OBSOLETE] Bone Marrow failure syndromes", "bone marrow failure syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bone marrow failure syndrome", "shortest_name_length": 28}
{"curie": "UMLS:C0573789", "names": ["heparin overdose", "overdose heparin", "Heparin overdose", "Heparin overdose (disorder)", "Heparin overdose (diagnosis)", "drug toxicity heparin overdose"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Heparin overdose", "shortest_name_length": 16}
{"curie": "MONDO:0012867", "names": ["SPG38", "hereditary spastic paraplegia 38", "hereditary spastic paraplegia type 38", "autosomal dominant spastic paraplegia 38", "Spastic Paraplegia 38, Autosomal Dominant", "SPASTIC PARAPLEGIA 38, AUTOSOMAL DOMINANT", "spastic paraplegia 38, autosomal dominant", "Autosomal dominant spastic paraplegia type 38", "autosomal dominant spastic paraplegia type 38", "SPASTIC PARAPLEGIA 38, AUTOSOMAL DOMINANT (disorder)", "Autosomal dominant spastic paraplegia type 38 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 38", "shortest_name_length": 5}
{"curie": "MONDO:0014368", "names": ["CMM10", "susceptibility to cutaneous malignant melanoma 10", "melanoma, cutaneous malignant, susceptibility to, 10", "MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 10", "melanoma, cutaneous malignant, susceptibility to, type 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melanoma, cutaneous malignant, susceptibility to, 10", "shortest_name_length": 5}
{"curie": "MONDO:0013081", "names": ["LPFS1", "ITK Deficiency", "ITK deficiency", "LYMPHOPROLIFERATIVE SYNDROME 1", "Lymphoproliferative Syndrome 1", "lymphoproliferative syndrome 1", "ITK lymphoproliferative syndrome", "lymphoproliferative syndrome type 1", "IL-2 Inducible T-cell Kinase Deficiency", "Lymphoproliferative Syndrome 1/ITK Deficiency", "Combined immunodeficiency due to ITK deficiency", "lymphoproliferative syndrome caused by mutation in ITK", "Lymphoproliferative Syndrome, Ebv-Associated, Autosomal, 1", "Autosomal recessive lymphoproliferative disease due to ITK deficiency", "Combined immunodeficiency due to IL2 inducible T cell kinase deficiency", "Combined immunodeficiency due to interleukin-2 inducible T cell kinase deficiency", "Combined immunodeficiency due to interleukin-2 inducible T cell kinase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphoproliferative syndrome 1", "shortest_name_length": 5}
{"curie": "MONDO:0003719", "names": ["renal pelvis tumor", "Renal Pelvis Tumor", "kidney pelvis tumor", "Kidney Pelvis Tumor", "Tumor of Renal Pelvis", "tumor of renal pelvis", "Tumor of renal pelvis", "renal pelvis neoplasm", "Renal Pelvis Neoplasm", "tumor of kidney pelvis", "Tumor of Kidney Pelvis", "Tumour of renal pelvis", "kidney pelvis neoplasm", "Kidney Pelvis Neoplasm", "tumor of kidney Pelvis", "neoplasm of renal pelvis", "Neoplasm of Renal Pelvis", "Neoplasm of renal pelvis", "Neoplasm of Kidney Pelvis", "tumor of the renal pelvis", "Tumor of the Renal Pelvis", "neoplasm of kidney pelvis", "Tumor of the Kidney Pelvis", "tumor of the kidney pelvis", "renal pelvis benign neoplasm", "neoplasm of the renal pelvis", "Neoplasm of the Renal Pelvis", "Neoplasm of the Kidney Pelvis", "neoplasm of the kidney pelvis", "renal pelvis neoplasm (disease)", "Neoplasm of renal pelvis (disorder)", "neoplasm of renal pelvis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal pelvis neoplasm", "shortest_name_length": 18}
{"curie": "UMLS:C5205261", "names": ["Rectal NET G2", "Rectal Neuroendocrine Tumor G2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rectal Neuroendocrine Tumor G2", "shortest_name_length": 13}
{"curie": "MONDO:0014230", "names": ["CANDF8", "candidiasis, familial, 8", "CANDIDIASIS, FAMILIAL, 8", "candidiasis, familial, type 8", "TRAF3IP2 chronic mucocutaneous candidiasis (disease)", "CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL RECESSIVE", "candidiasis, familial chronic mucocutaneous, autosomal recessive", "chronic mucocutaneous candidiasis (disease) caused by mutation in TRAF3IP2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "candidiasis, familial, 8", "shortest_name_length": 6}
{"curie": "UMLS:C2984088", "names": ["Colon Cancer by AJCC v7 Stage", "Colon Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colon Cancer by AJCC v7 Stage", "shortest_name_length": 29}
{"curie": "EFO:1001864", "names": ["uterine prolapse"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine prolapse", "shortest_name_length": 16}
{"curie": "UMLS:C5670674", "names": ["Stage IB2 Cervical Cancer FIGO 2009", "Stage IB2 Cervical Carcinoma FIGO 2009"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB2 Cervical Cancer FIGO 2009", "shortest_name_length": 35}
{"curie": "MONDO:0006876", "names": ["eye; tuberculous", "tuberculosis eye", "eye tuberculosis", "eyes tuberculosis", "tuberculosis; eye", "Tuberculosis of eye", "Ocular Tuberculosis", "tuberculosis ocular", "Ocular tuberculosis", "ocular tuberculosis", "Ocular Tuberculoses", "tuberculosis of eye", "Tuberculoses, Ocular", "Eye tuberculosis NOS", "Tuberculosis, Ocular", "Tuberculosis of eye, NOS", "Tuberculosis of eye (disorder)", "tuberculosis of eye (diagnosis)", "Tuberculosis of eye, unspecified", "Tuberculosis of eye, unspecified examination"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ocular tuberculosis", "shortest_name_length": 16}
{"curie": "UMLS:C1333313", "names": ["Drop Metastasis in the Spinal Cord", "Drop Metastasis to the Spinal Cord", "Drop Metastatic Tumor to the Spinal Cord", "Drop Metastatic Neoplasm to the Spinal Cord", "Drop Secondary Malignant Tumor to the Spinal Cord", "Drop Secondary Malignant Neoplasm to the Spinal Cord"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drop Metastasis in the Spinal Cord", "shortest_name_length": 34}
{"curie": "UMLS:C4744856", "names": ["Metastatic Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Neuroendocrine Neoplasm", "shortest_name_length": 34}
{"curie": "MONDO:0005899", "names": ["parotid disease", "Parotid Disease", "Parotid Diseases", "parotid diseases", "parotid disorder", "Disease, Parotid", "Diseases, Parotid", "parotid gland disease", "disease of parotid gland", "disorder of parotid gland", "parotid gland disease or disorder", "disease or disorder of parotid gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parotid disorder", "shortest_name_length": 15}
{"curie": "MONDO:0002770", "names": ["fluor vaginalis", "Fluor vaginalis", "vagina discharge", "VAGINA DISCHARGE", "Vaginal discharge", "discharge; vagina", "Discharge;vaginal", "Vaginal Discharge", "vaginal discharge", "VAGINAL DISCHARGE", "Discharge vaginal", "DISCHARGE VAGINAL", "vagina; discharge", "Discharge, vaginal", "Vaginal Discharges", "Discharge, Vaginal", "vaginal discharges", "Discharges, Vaginal", "vaginal discharge nos", "Vaginal discharge NOS", "Vaginal discharge problem", "Vaginal discharge syndrome", "Abnormal vaginal discharge", "Abnormal Vaginal Discharge", "Vaginal discharge (finding)", "vaginal discharge (diagnosis)", "Observation of vaginal discharge", "Vaginal discharge problem (finding)", "vaginal discharge (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vaginal discharge", "shortest_name_length": 15}
{"curie": "UMLS:C0751884", "names": ["Presynaptic Congenital Myasthenic Syndrome", "Presynaptic congenital myasthenic syndromes", "Presynaptic Congenital Myasthenic Syndromes", "Congenital Myasthenic Syndromes, Presynaptic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Myasthenic Syndromes, Presynaptic", "shortest_name_length": 42}
{"curie": "MONDO:0004698", "names": ["intestine carcinoma in situ", "stage 0 intestine carcinoma", "intestine in situ carcinoma", "carcinoma in situ of intestine", "Carcinoma in situ of intestine", "Carcinoma in situ of intestinal tract", "carcinoma in situ of intestine (diagnosis)", "Carcinoma in situ of intestinal tract, NOS", "Carcinoma in situ of intestinal tract (disorder)", "Carcinoma in situ of other and unspecified parts of intestine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intestine carcinoma in situ", "shortest_name_length": 27}
{"curie": "UMLS:C0854092", "names": ["Septic arthritis staphylococcal", "Staphylococcal Septic Arthritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Septic arthritis staphylococcal", "shortest_name_length": 31}
{"curie": "UMLS:C0038166", "names": ["STAPHYLOCOCCAL SKIN DISEASE", "Staphylococcal Skin Diseases", "Staphylococcal skin disorder", "Staphylococcal skin infection", "infection skin staphylococcal", "Skin Diseases, Staphylococcal", "Staphylococcal Diseases, Skin", "staphylococcal skin infection", "Staphylococcal Skin Infections", "staphylococcal skin infections", "Skin Infections, Staphylococcal", "Staphylococcal Infections, Skin", "Infections, Staphylococcal Skin", "Staphylococcal infection of skin", "staphylococcal infection skin disorder", "Staphylococcal skin disorder (diagnosis)", "Staphylococcal infection of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Staphylococcal Skin Infections", "shortest_name_length": 27}
{"curie": "UMLS:C0029225", "names": ["organic; delusional", "delusional; organic", "Paranoid organic state", "organic; paranoid state", "paranoid; state, organic", "state; paranoid, organic", "ORGANIC DELUSIONAL SYNDROME", "Organic delusional disorder", "Organic Delusional Syndrome", "Organic delusional syndrome", "organic delusional disorder", "DELUSIONAL DISORDER ORGANIC", "organic delusional syndrome", "delusional disorder organic", "disorder; delusional, organic", "disorder; organic, delusional", "organic; disorder, delusional", "Organic delusional disorder, NOS", "Organic delusional disorder (disorder)", "Organic delusional disorder (diagnosis)", "Organic delusional [schizophrenia-like] disorder", "Transient organic psychotic condition, paranoid type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Organic delusional disorder", "shortest_name_length": 19}
{"curie": "MONDO:0017493", "names": ["fibular hemimelia, bilateral", "fibular longitudinal meromelia, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibular hemimelia, bilateral", "shortest_name_length": 28}
{"curie": "UMLS:C4683556", "names": ["Lymphoma by Ann Arbor Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoma by Ann Arbor Stage", "shortest_name_length": 27}
{"curie": "UMLS:C1333444", "names": ["Esophageal NET G1", "Esophageal Carcinoid Tumor", "Carcinoid Tumor of Esophagus", "Esophageal NET G1 (Carcinoid)", "Carcinoid Tumor of the Esophagus", "Esophageal Neuroendocrine Tumor G1", "malignant carcinoid tumor of esophagus", "Esophageal Neuroendocrine Tumor G1 (Carcinoid)", "malignant carcinoid tumor of esophagus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Neuroendocrine Tumor G1", "shortest_name_length": 17}
{"curie": "MONDO:0017216", "names": ["Calciphylaxis cutis", "calciphylaxis cutis", "Calciphylaxis cutis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "calciphylaxis cutis", "shortest_name_length": 19}
{"curie": "UMLS:C0853709", "names": ["Recurrent Waldenstrom Macroglobulinemia", "Waldenstrom's macroglobulinemia recurrent", "Waldenstrom's macroglobulinaemia recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Waldenstrom's macroglobulinemia recurrent", "shortest_name_length": 39}
{"curie": "MONDO:0012809", "names": ["AFH", "Angiomatoid fibrous histiocytoma", "angiomatoid fibrous histiocytoma", "Angiomatoid Fibrous Histiocytoma", "histiocytoma, Angiomatoid fibrous", "HISTIOCYTOMA, ANGIOMATOID FIBROUS", "Histiocytoma, Angiomatoid Fibrous", "histiocytoma, angiomatoid fibrous, somatic", "angiomatoid malignant fibrous histiocytoma", "Angiomatoid Malignant Fibrous Histiocytoma", "Angiomatoid fibrous histiocytoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "histiocytoma, Angiomatoid fibrous", "shortest_name_length": 3}
{"curie": "MONDO:0009147", "names": ["HED", "EDA", "ECTD10B", "ectodermal dysplasia 10B", "ECTODERMAL DYSPLASIA, ANHIDROTIC", "ectodermal dysplasia, anhidrotic", "ECTODERMAL DYSPLASIA, HYPOHIDROTIC", "ectodermal dysplasia, hypohidrotic", "ectodermal dysplasia 10B, hypohidrotic/hair/nail type, autosomal recessive", "ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive", "ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive", "shortest_name_length": 3}
{"curie": "UMLS:C4683675", "names": ["Mature T- and NK-Cell Lymphoma by Ann Arbor Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mature T- and NK-Cell Lymphoma by Ann Arbor Stage", "shortest_name_length": 49}
{"curie": "MONDO:0000642", "names": ["brain meningioma", "brain meningioma (disease)", "meningioma (disease) of brain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brain meningioma", "shortest_name_length": 16}
{"curie": "UMLS:C0854119", "names": ["rupture appendicitis", "Ruptured Appendicitis", "ruptured appendicitis", "Appendicitis, Ruptured", "Appendicitis perforated", "appendicitis perforated", "perforated appendicitis", "Perforated Appendicitis", "Appendicitis, Perforated", "Appendicitis with rupture"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ruptured Appendicitis", "shortest_name_length": 20}
{"curie": "MONDO:0003406", "names": ["Problem;sleep", "Sleep problem", "sleep problem", "Sleep disorder", "Sleep Disorder", "sleep disorder", "Disorder sleep", "DISORDER SLEEP", "Disorder;sleep", "SLEEP DISORDER", "Sleep Disorders", "disorder, sleep", "SLEEP DISORDERS", "sleep disorders", "Disorder, Sleep", "Sleep disorders", "Disorders, Sleep", "disorders, sleep", "Sleeping problems", "Sleep Disturbance", "sleep disturbance", "Sleep disorder NOS", "sleeping disorders", "sleep disturbances", "sleep-wake disorder", "Sleep-wake disorder", "Sleep disorder, NOS", "Sleep Wake Disorder", "sleep wake disorder", "wake disorder, sleep", "Wake Disorder, Sleep", "Sleep wake disorders", "Disorder, Sleep Wake", "disorder, sleep wake", "Sleep Wake Disorders", "SLEEP DISORDER (NOS)", "disorders, sleep wake", "long sleeper syndrome", "short sleep phenotype", "Wake Disorders, Sleep", "wake disorders, sleep", "Disorders, Sleep Wake", "short sleep phenotypes", "short sleeper syndrome", "long sleeper syndromes", "syndrome, long sleeper", "sleeper syndrome, long", "phenotype, short sleep", "sleeper syndromes, long", "syndrome, short sleeper", "syndromes, long sleeper", "phenotypes, short sleep", "short sleeper syndromes", "sleeper syndrome, short", "circadian dysregulation", "sleep phenotypes, short", "syndromes, short sleeper", "sleeper syndromes, short", "Subwakefullness syndrome", "syndrome, Subwakefullness", "Sleep disorder (disorder)", "Subwakefullness syndromes", "Non-organic sleep disorder", "syndromes, Subwakefullness", "non-organic sleep disorder", "sleep disorder (diagnosis)", "Sleep disorder, unspecified", "disorder of sleep-wake cycle", "disturbed nyctohemeral rhythm", "disorder of sleep-wake schedule", "Sleep disorders and disturbances", "sleep related neurogenic tachypnea", "sleep-related neurogenic tachypnea", "tachypnea, sleep-related neurogenic", "sleep-related neurogenic Tachypneas", "neurogenic tachypnea, sleep-related", "disorders of the sleep-wake schedule", "Tachypneas, sleep-related neurogenic", "neurogenic Tachypneas, sleep-related", "Specific disorders of sleep of nonorganic origin", "Specific disorders of sleep of non-organic origin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sleep-wake disorder", "shortest_name_length": 13}
{"curie": "UMLS:C0265222", "names": ["Royer Syndrome", "Royers Syndrome", "Syndrome, Royer", "Royer's syndrome", "Royer's Syndrome", "Syndrome, Royer's", "Prader-Willi syndrome and diabetes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Royer Syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0700003", "names": ["obstetric disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "obstetric disorder", "shortest_name_length": 18}
{"curie": "MONDO:0010711", "names": ["TARPS", "TARP SYNDROME", "TARP syndrome", "tarp syndrome", "TARP syndrome, X-linked recessive", "Pierre Robin sequence - congenital heart defect - talipes", "Pierre Robin syndrome - congenital heart defect - talipes", "Pierre Robin sequence-congenital heart defect-talipes syndrome", "Pierre Robin syndrome-congenital heart defect-talipes syndrome", "Pierre Robin sequence, congenital heart defect, talipes syndrome", "Pierre Robin syndrome, congenital heart defect, talipes syndrome", "PIERRE ROBIN SYNDROME WITH CONGENITAL HEART MALFORMATION AND CLUBFOOT", "Pierre Robin syndrome with congenital heart malformation and clubfoot", "Pierre Robin sequence, congenital heart defect, talipes syndrome (disorder)", "Talipes Equinovarus, Atrial Septal Defect, Robin Sequence, and Persistence of Left Superior Vena Cava", "TALIPES EQUINOVARUS, ATRIAL SEPTAL DEFECT, ROBIN SEQUENCE, AND PERSISTENCE OF LEFT SUPERIOR VENA CAVA", "talipes equinovarus, atrial septal defect, Robin sequence, and persistence of left Superior vena cava", "talipes equinovarus - atrial septal defect - Robin sequence - persistence of the left superior vena cava", "Talipes equinovarus-atrial septal defect-Robin sequence-persistence of the left superior vena cava syndrome", "talipes equinovarus-atrial septal defect-Robin sequence-persistence of the left superior vena cava syndrome", "TARP (talipes equinovarus, atrial septal defect, Robin sequence, persistence of left superior vena cava) syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "TARP syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C5237059", "names": ["Refractory Endometrial Transitional Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Endometrial Transitional Cell Carcinoma", "shortest_name_length": 50}
{"curie": "UMLS:C1112375", "names": ["cataract operation complication", "Cataract operation complication", "cataract complications operation", "cataract complications operations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cataract operation complication", "shortest_name_length": 31}
{"curie": "UMLS:C2825131", "names": ["APL with t(11;17)(q13;q21); NUMA1-RARA", "Acute Myeloid Leukemia with t(11;17)(q13;q21)", "Acute Promyelocytic Leukemia with t(11;17)(q13;q21); NUMA1-RARA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Myeloid Leukemia with t(11;17)(q13;q21)", "shortest_name_length": 38}
{"curie": "MONDO:0013046", "names": ["GSD13", "GSD 13", "GSDXIII", "GSD XIII", "enolase 3 deficiency", "glycogenosis type 13", "ENOLASE 3 DEFICIENCY", "Enolase 3 Deficiency", "enolase-Beta deficiency", "ENOLASE-BETA DEFICIENCY", "Enolase-Beta Deficiency", "muscle enolase deficiency", "muscular enolase deficiency", "glycogen storage disease 13", "Glycogen Storage Disease XIII", "glycogen storage disease XIII", "GLYCOGEN STORAGE DISEASE XIII", "glycogen storage disease type 13", "GSD due to muscle beta-enolase deficiency", "glycogenosis due to muscle beta-enolase deficiency", "glycogen storage disease due to muscle beta-enolase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease due to muscle beta-enolase deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0010497", "names": ["MRXSSB", "MRX102", "MRX102, FORMERLY", "Mental Retardation, X-linked 102", "MENTAL RETARDATION, X-LINKED 102", "mental retardation, X-linked 102", "mental retardation, X-linked type 102", "intellectual disability, X-linked 102", "DDX3X-related intellectual disability", "MENTAL RETARDATION, X-LINKED 102, FORMERLY", "intellectual disability, X-linked type 102", "DDX3X non-syndromic X-linked intellectual disability", "non-syndromic X-linked intellectual disability caused by mutation in DDX3X", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE", "intellectual developmental disorder, X-linked, syndrome, Snijders Blok type, X-linked recessive, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 102", "shortest_name_length": 6}
{"curie": "MONDO:0014105", "names": ["HH19", "DUSP6 hypogonadotropic hypogonadism", "HYPOGONADOTROPIC HYPOGONADISM 19 WITH OR WITHOUT ANOSMIA", "hypogonadotropic hypogonadism 19 with or without anosmia", "hypogonadotropic hypogonadism caused by mutation in DUSP6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadotropic hypogonadism 19 with or without anosmia", "shortest_name_length": 4}
{"curie": "MONDO:0100276", "names": ["peroxisome and mitochronrial fission disease", "disorder of defective peroxisomal and mitochondrial fission"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of defective peroxisomal and mitochondrial fission", "shortest_name_length": 44}
{"curie": "MONDO:0001549", "names": ["HUS", "renal ttp", "kidney ttp", "GASSER SYNDROME", "Gasser Syndrome", "gasser syndrome", "Gassers Syndrome", "Gasser's syndrome", "Gasser's Syndrome", "Hemolytic uremic syndrome", "HEMOLYTIC-UREMIC SYNDROME", "hemolytic uremic syndrome", "Hemolytic-Uremic Syndrome", "SYNDROME HEMOLYTIC UREMIC", "Syndrome hemolytic uremic", "Hemolytic-uremic syndrome", "hemolytic-uremic syndrome", "HEMOLYTIC UREMIC SYNDROME", "Hemolytic Uremic Syndrome", "syndrome; hemolytic-uremic", "hemolytic-uremic; syndrome", "Syndrome, Hemolytic-Uremic", "Syndrome haemolytic uraemic", "haemolytic-uraemic syndrome", "HAEMOLYTIC-URAEMIC SYNDROME", "Haemolytic uraemic syndrome", "Haemolytic-uraemic syndrome", "Hemolytic-uremic syndrome NOS", "Hemolytic uremic syndrome, NOS", "HUS - Hemolytic uremic syndrome", "HUS (hemolytic uremic syndrome)", "hemolytic-uremic syndrome (HUS)", "Haemolytic uraemic syndrome, NOS", "HUS - Haemolytic uraemic syndrome", "Hemolytic uremic syndrome (disorder)", "hemolytic uremic syndrome (diagnosis)", "Hemolytic-uremic syndrome, unspecified", "RENAL THROMBOTIC THROMBOCYTOPENIC PURPURA HEMOLYTIC UREMIC SYNDROME", "kidney thrombotic thrombocytopenic purpura hemolytic uremic syndrome", "RENAL THROMBOTIC THROMBOCYTOPENIC PURPURA <HEMOLYTIC UREMIC SYNDROME>", "acute renal failure, thrombocytopenia, and microangiopathic hemolytic anemia associated with distorted erythrocytes ('burr cells')"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemolytic-uremic syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0008637", "names": ["Cleft uvula", "cleft uvula", "bifid uvula", "Split uvula", "uvula cleft", "uvula bifid", "Bifid uvula", "UVULA, BIFID", "Uvular cleft", "cleft; uvula", "uvula, bifid", "uvula; bifid", "bifid; uvula", "Uvula bifida", "uvula, cleft", "uvula bifida", "Forked uvula", "UVULA, CLEFT", "uvula; cleft", "uvular cleft", "Cleft of uvula", "Bifid palatine uvula", "Bifidity of the uvula", "bifidity of the uvula", "Cleft uvula (disorder)", "cleft uvula (diagnosis)", "cleft uvula (physical finding)", "bifid uvula (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bifid uvula", "shortest_name_length": 11}
{"curie": "MONDO:0004375", "names": ["ESRD", "CKD stage 5", "Chronic renal failure", "end stage renal disease", "End stage renal disease", "Renal failure, endstage", "End stage renal failure", "End-stage renal failure", "End-stage renal disease", "End-stage Renal Disease", "End Stage Renal Disease", "End Stage Renal Failure", "End-Stage Renal Disease", "end stage renal failure", "end-stage kidney disease", "end stage kidney failure", "renal disease, end stage", "End Stage Kidney Failure", "End Stage Kidney Disease", "end stage kidney disease", "ESRD, end stage renal disease", "Stage 5 chronic kidney disease", "end stage renal disease (ESRD)", "Chronic kidney disease stage 5", "chronic kidney disease stage 5", "renal disease (ESRD), end stage", "disease (ESRD), end stage renal", "Chronic Kidney Disease, Stage 5", "chronic kidney disease, stage 5", "Chronic kidney disease, stage 5", "Chronic kidney disease stage 5 (disorder)", "chronic kidney disease stage 5 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "end stage renal failure", "shortest_name_length": 4}
{"curie": "UMLS:C1335003", "names": ["Non-Neoplastic Connective and Soft Tissue Disease", "Non-Neoplastic Connective and Soft Tissue Disorder", "Non-Neoplastic Connective and Soft Tissue Diseases", "Non-Neoplastic Connective and Soft Tissue Disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Connective and Soft Tissue Disorder", "shortest_name_length": 49}
{"curie": "MONDO:0017526", "names": ["bilateral PPD2", "preaxial polydactyly type 2, bilateral", "polydactyly of a triphalangeal thumb, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polydactyly of a triphalangeal thumb, bilateral", "shortest_name_length": 14}
{"curie": "UMLS:C5555739", "names": ["Oligometastatic Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oligometastatic Breast Carcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C0854482", "names": ["Device leakage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Device leakage", "shortest_name_length": 14}
{"curie": "UMLS:C0428982", "names": ["Nodal Tachycardia", "nodal tachycardia", "NODAL TACHYCARDIA", "Tachycardia nodal", "tachycardia nodal", "Nodal tachycardia", "TACHYCARDIA NODAL", "tachycardia; nodal", "nodal; tachycardia", "AV junctional tachycardia", "A-V junctional tachycardia", "Accelerated junctional rhythm", "AV junctional (nodal) tachycardia", "A-V junctional tachycardia (diagnosis)", "Atrioventricular junctional (nodal) tachycardia", "Atrioventricular junctional (nodal) tachycardia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AV junctional (nodal) tachycardia", "shortest_name_length": 17}
{"curie": "MONDO:0011004", "names": ["lissencephaly type 3 and bone dysplasia", "lissencephaly type III and bone dysplasia", "LISSENCEPHALY TYPE III AND BONE DYSPLASIA", "Lissencephaly Type III and Bone Dysplasia", "lissencephaly type 3-metacarpal bone dysplasia syndrome", "Lissencephaly type 3 metacarpal bone dysplasia syndrome", "Lissencephaly type 3-metacarpal bone dysplasia syndrome", "Lissencephaly type 3 metacarpal bone dysplasia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lissencephaly type 3-metacarpal bone dysplasia syndrome", "shortest_name_length": 39}
{"curie": "MONDO:0032876", "names": ["NEDALVS", "ITO-RAYMOND SYNDROME", "Ito-Raymond Syndrome", "neurodevelopmental disorder with absent language and variable seizures", "NEURODEVELOPMENTAL DISORDER WITH ABSENT LANGUAGE AND VARIABLE SEIZURES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with absent language and variable seizures", "shortest_name_length": 7}
{"curie": "UMLS:C0033950", "names": ["inhibited sexual arousal", "Psychosexual Dysfunction with Inhibited Sexual Excitement", "psychosexual dysfunction with inhibited sexual excitement", "Psychosexual dysfunction with inhibited sexual excitement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Psychosexual dysfunction with inhibited sexual excitement", "shortest_name_length": 24}
{"curie": "MONDO:8000008", "names": ["MARTS", "MARTS1", "MARTSOLF SYNDROME", "MARTSOLF syndrome", "Martsolf syndrome", "MARTSOLF SYNDROME 1", "Martsolf syndrome 1", "CATARACT-MENTAL RETARDATION-HYPOGONADISM", "Cataract-Mental Retardation-Hypogonadism", "cataract-mental retardation-hypogonadism", "Cataract, mental retardation, hypogonadism", "cataract-intellectual disability-hypogonadism", "cataract-mental retardation-hypogonadism syndrome", "cataract-intellectual disability-hypogonadism syndrome", "Cataract-intellectual disability-hypogonadism syndrome", "microcephaly-mental retardation-cataract-hypogonadism syndrome", "Congenital cataract with intellectual disability and hypogonadotropic hypogonadism syndrome", "congenital cataract with intellectual disability and hypogonadotropic hypogonadism syndrome", "Congenital cataract with intellectual disability and hypogonadotropic hypogonadism syndrome (disorder)", "congenital cataract with intellectual disability and hypogonadotropic hypogonadism syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Martsolf syndrome 1", "shortest_name_length": 5}
{"curie": "MONDO:0005636", "names": ["Adenosarcoma", "adenosarcoma", "Adenosarcomas", "[M]Adenosarcoma", "Mullerian adenosarcoma", "mullerian adenosarcoma", "Mullerian Adenosarcoma", "Müllerian adenosarcoma", "Müllerian Adenosarcoma", "mullerian Adenosarcoma", "Adenosarcoma (morphologic abnormality)", "adenosarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenosarcoma", "shortest_name_length": 12}
{"curie": "UMLS:C5238705", "names": ["Syndrome", "Genetic Syndrome Associated with Congenital Heart Defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Genetic Syndrome Associated with Congenital Heart Defect", "shortest_name_length": 8}
{"curie": "MONDO:0018987", "names": ["Granulomatis mastitis", "granulomatous mastitis", "mastitis granulomatous", "Granulomatous mastitis", "Granulomatous Mastitis", "Mastitis, Granulomatous", "granulomatous lobular mastitis", "Granulomatous mastitis (disorder)", "Idiopathic granulomatous mastitis", "idiopathic granulomatous mastitis", "Granulomatous mastitis (diagnosis)", "idiopathic granulomatous lobular mastitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "granulomatous mastitis", "shortest_name_length": 21}
{"curie": "MONDO:0032579", "names": ["WRCN", "warburg-cinotti syndrome", "WARBURG-CINOTTI SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "warburg-cinotti syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C1336222", "names": ["Gastric Cancer Stage IIIB", "Stage IIIB Gastric Cancer", "Stage IIIB Stomach Carcinoma", "Stomach Carcinoma Stage IIIB", "Gastric Carcinoma Stage IIIB", "Stage IIIB Gastric Carcinoma", "Stage IIIB Carcinoma of Stomach", "Carcinoma of Stomach Stage IIIB", "Stage IIIB Gastric Cancer AJCC v7", "Stage IIIB Carcinoma of the Stomach", "Stage IIIB Gastric (Stomach) Cancer", "Carcinoma of the Stomach Stage IIIB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Gastric Carcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0000676", "names": ["phonagnosia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phonagnosia", "shortest_name_length": 11}
{"curie": "UMLS:C4524853", "names": ["Recurrent Primary Amyloidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Primary Amyloidosis", "shortest_name_length": 29}
{"curie": "UMLS:C0271909", "names": ["Drug induced aplastic anemia", "Drug-Induced Aplastic Anemia", "aplastic anemia due to drugs", "Drug-induced aplastic anemia", "Aplastic anemia due to drugs", "Drug induced aplastic anaemia", "Aplastic anaemia due to drugs", "anemia; aplastic due to drugs", "Drug-induced aplastic anaemia", "Aplastic anemia secondary to drugs", "Aplastic anaemia secondary to drugs", "Aplastic anemia due to drugs (disorder)", "aplastic anemia due to drugs (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aplastic anemia due to drugs", "shortest_name_length": 28}
{"curie": "MONDO:0022403", "names": ["Argonz Del Castillo syndrome", "Ahumada Del Castillo syndrome", "nonpuerperal galactorrhe amenorrhea", "Argonz Ahumada Del Castillo syndrome", "galactorrhea amenorrhea without pregnancy", "amenorrhea galactorrhea FSH decrease syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ahumada Del Castillo syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0015171", "names": ["Congenital enterocyte heparan sulfate deficiency", "congenital enterocyte heparan sulfate deficiency", "Congenital enterocyte heparan sulphate deficiency", "Congenital enterocyte heparan sulfate deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital enterocyte heparan sulfate deficiency", "shortest_name_length": 48}
{"curie": "UMLS:C1332938", "names": ["Acute Leukemia in Remission", "Childhood Acute Leukemia in Remission"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Acute Leukemia in Remission", "shortest_name_length": 27}
{"curie": "MONDO:0016100", "names": ["Rmd-MG", "acquired rippling muscle disease", "immune-mediated rippling muscle disease", "rippling muscle disease with myasthenia gravis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rippling muscle disease with myasthenia gravis", "shortest_name_length": 6}
{"curie": "UMLS:C1335444", "names": ["poorly differentiated cancer", "cancer poorly differentiated", "CANCER DIFFERENTIATED POORLY", "cancer differentiated poorly", "Poorly Differentiated Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Poorly Differentiated Malignant Neoplasm", "shortest_name_length": 28}
{"curie": "MONDO:0035605", "names": ["B-lymphoblastic leukemia/lymphoma with recurrent genetic abnormality", "B Lymphoblastic Leukemia/Lymphoma with Recurrent Genetic Abnormalities", "B-Lymphoblastic Leukemia/Lymphoma with Recurrent Genetic Abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-lymphoblastic leukemia/lymphoma with recurrent genetic abnormality", "shortest_name_length": 68}
{"curie": "MONDO:0014820", "names": ["MTDPS14", "mitochondrial DNA depletion syndrome 14", "OPA1 mitochondrial DNA depletion syndrome", "mitochondrial DNA depletion syndrome caused by mutation in OPA1", "mitochondrial DNA depletion syndrome 14 (encephalocardiomyopathic type)", "MITOCHONDRIAL DNA DEPLETION SYNDROME 14 (CARDIOENCEPHALOMYOPATHIC TYPE)", "mitochondrial DNA depletion syndrome 14 (cardioencephalomyopathic type)", "mitochondrial DNA depletion syndrome 14 (cardioencephalomyopathic type); MTDPS14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial DNA depletion syndrome 14 (cardioencephalomyopathic type)", "shortest_name_length": 7}
{"curie": "UMLS:C2830012", "names": ["Reactive Gastritis", "Chemical Gastritis", "Chemical gastritis", "Reactive gastritis", "chemical gastritis", "Reactive Gastropathy", "Chemical gastropathy", "Chemical Gastropathy", "RG - Reactive gastritis", "Reactive gastritis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chemical Gastritis", "shortest_name_length": 18}
{"curie": "MONDO:0011824", "names": ["AUTS8", "AUTS2", "AUTS2, FORMERLY", "AUTS2, formerly", "autism, susceptibility to, 8", "AUTISM, SUSCEPTIBILITY TO, 8", "autism susceptibility 8, isolated cases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autism, susceptibility to, 8", "shortest_name_length": 5}
{"curie": "UMLS:C0007814", "names": ["CSF otorrhea", "Cerebrospinal Otorrhea", "Cerebrospinal otorrhea", "Cerebrospinal otorrhoea", "otorrhea; cerebrospinal", "Otorrhea, Cerebrospinal", "cerebrospinal; otorrhea", "Cerebrospinal Fluid Otorrhea", "CSF - Cerebrospinal otorrhea", "cerebrospinal fluid otorrhea", "Cerebrospinal fluid otorrhea", "Cerebrospinal fluid otorrhoea", "Otorrhea, Cerebrospinal Fluid", "CSF - Cerebrospinal otorrhoea", "Cerebrospinal Fluid Otorrheas", "CSF - Cerebrospinal fluid otorrhea", "CSF - Cerebrospinal fluid otorrhoea", "Cerebrospinal fluid otorrhea (disorder)", "cerebrospinal fluid otorrhea (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebrospinal Fluid Otorrhea", "shortest_name_length": 12}
{"curie": "MONDO:0006913", "names": ["PNEUMOCOCCAL MENINGITIS", "MENINGITIS PNEUMOCOCCAL", "meningitis pneumococcal", "pneumococcal meningitis", "Pneumococcal Meningitis", "Meningitis pneumococcal", "Pneumococcal meningitis", "MENINGITIS, PNEUMOCOCCAL", "pneumococcal; meningitis", "meningitis; pneumococcal", "Meningitis, Pneumococcal", "Pneumococcal Meningitides", "Pneumococcal meningitis (disorder)", "pneumococcal meningitis (diagnosis)", "Streptococcus pneumoniae Meningitis", "Streptococcus pneumoniae meningitis", "Meningitis, Streptococcus pneumoniae", "Streptococcus pneumoniae Meningitides", "Meningitides, Streptococcus pneumoniae", "Meningtitis due to Streptococcal pneumoniae", "Streptococcus pneumoniae infectious meningitis", "Streptococcus pneumoniae caused infectious meningitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pneumococcal meningitis", "shortest_name_length": 23}
{"curie": "MONDO:0030934", "names": ["MRD64", "mental retardation, autosomal dominant 64", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 64", "intellectual developmental disorder, autosomal dominant 64", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 64"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder, autosomal dominant 64", "shortest_name_length": 5}
{"curie": "MONDO:0004244", "names": ["PTES", "Central Epithelioid Sarcoma", "central epithelioid sarcoma", "Large Cell Epithelioid Sarcoma", "Proximal-Type Epithelioid Sarcoma", "proximal-type epithelioid sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "proximal-type epithelioid sarcoma", "shortest_name_length": 4}
{"curie": "UMLS:C0271899", "names": ["normocytic normochromic anemia", "anemia normochromic normocytic", "ANEMIA NORMOCYTIC NORMOCHROMIC", "normochromic normocytic anemia", "Normochromic normocytic anemia", "Normocytic normochromic anemia", "Normocytic normochromic anaemia", "Normochromic normocytic anaemia", "normochromic, normocytic anemia", "normochromic normocytic anaemia", "Normocytic normochromic anemia (disorder)", "normocytic normochromic anemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Normocytic normochromic anemia", "shortest_name_length": 30}
{"curie": "MONDO:0018523", "names": ["pancreas mucinous cystadenoma", "Pancreatic Colloid Cystadenoma", "pancreatic colloid cystadenoma", "pancreatic mucinous cystadenoma", "colloid cystadenoma of pancreas", "Colloid Cystadenoma of Pancreas", "Pancreatic Mucinous Cystadenoma", "Pancreatic mucinous cystadenoma", "Mucinous Cystadenoma of Pancreas", "pancreatic colloidal cystadenoma", "Pancreatic Colloidal Cystadenoma", "mucinous Cystadenoma of pancreas", "mucinous cystadenoma of pancreas", "Mucinous cystadenoma of pancreas", "Colloidal Cystadenoma of Pancreas", "colloidal cystadenoma of pancreas", "pancreatic mucinous cystic neoplasm", "Colloid Cystadenoma of the Pancreas", "colloid cystadenoma of the pancreas", "Mucinous Cystadenoma of the Pancreas", "mucinous cystadenoma of the pancreas", "colloidal cystadenoma of the pancreas", "Colloidal Cystadenoma of the Pancreas", "pancreatic mucinous cystadenocarcinoma", "mucinous cystadenocarcinoma of the pancreas", "Mucinous cystadenoma of pancreas (disorder)", "mucinous cystadenoma of pancreas (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic mucinous cystadenoma", "shortest_name_length": 29}
{"curie": "MONDO:0013405", "names": ["RP49", "retinitis pigmentosa 49", "RETINITIS PIGMENTOSA 49", "CNGA1 retinitis pigmentosa", "retinitis pigmentosa type 49", "retinitis pigmentosa caused by mutation in CNGA1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 49", "shortest_name_length": 4}
{"curie": "MONDO:0001636", "names": ["Mechanical entropion", "mechanical entropion", "Mechanical entropion (disorder)", "mechanical entropion (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mechanical entropion", "shortest_name_length": 20}
{"curie": "MONDO:0014626", "names": ["SCA41", "cerebellar ataxia type 41", "SPINOCEREBELLAR ATAXIA 41", "spinocerebellar ataxia 41", "Spinocerebellar ataxia type 41", "spinocerebellar ataxia type 41", "Spinocerebellar ataxia type 41 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia type 41", "shortest_name_length": 5}
{"curie": "MONDO:0005865", "names": ["Mushroom Worker Lung", "shimeji worker's lung", "mushroom workers lung", "Mushroom Workers Lung", "Mushroom workers lung", "Mushroom workers' lung", "mushroom workers' lung", "Mushroom-workers' lung", "shiitaki worker's lung", "Mushroom Worker's Lung", "pholiota worker's lung", "Mushroom-worker's lung", "pleurotus worker's lung", "Mushroom Worker's Lungs", "MUSHROOM PICKER DISEASE", "mushroom growers' disease", "Mushroom pickers' disease", "bunashimeji worker's lung", "Mushroom-workers' disease", "Mushroom-worker's disease", "mushroom-worker's disease or lung", "Mushroom workers' lung (disorder)", "mushroom growers' disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mushroom workers' lung", "shortest_name_length": 20}
{"curie": "MONDO:0015203", "names": ["coronary artery congenital malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coronary artery congenital malformation", "shortest_name_length": 39}
{"curie": "OMIM:617749", "names": ["ACTN3 DEFICIENCY", "ALPHA-ACTININ-3 DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 16}
{"curie": "MONDO:0008847", "names": ["APL", "papular atrichia", "Papular atrichia", "PAPULAR ATRICHIA", "Papular Atrichia", "Atrichia with papular lesions", "atrichia with papular lesions", "Atrichia with Papular Lesions", "ATRICHIA WITH PAPULAR LESIONS", "Atrichia with papular lesions (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrichia with papular lesions", "shortest_name_length": 3}
{"curie": "MONDO:0010348", "names": ["DYX9", "dyslexia, susceptibility to, 9", "DYSLEXIA, SUSCEPTIBILITY TO, 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyslexia, susceptibility to, 9", "shortest_name_length": 4}
{"curie": "MONDO:0005304", "names": ["biliary tumor", "Biliary tumor", "biliary neoplasm", "Biliary neoplasm", "Biliary neoplasia", "BILIARY NEOPLASIA", "biliary tree tumor", "Biliary neoplasm NOS", "biliary tree neoplasm", "tumor of biliary tree", "Biliary tract neoplasm", "biliary tract neoplasm", "Biliary Tract Neoplasm", "NEOPLASM BILIARY TRACT", "Tumor of biliary tract", "Neoplasm biliary tract", "Neoplasm, Biliary Tract", "Tumour of biliary tract", "Biliary Tract Neoplasms", "biliary tract neoplasms", "Neoplasms, Biliary Tract", "neoplasm of biliary tree", "Neoplasm of biliary tract", "biliary tract benign neoplasm", "Neoplasia of the biliary tract", "biliary tree neoplasm (disease)", "extrahepatic bile duct neoplasm", "biliary tract neoplasm (disease)", "tumor of the extrahepatic bile duct", "neoplasm of extrahepatic bile ducts", "Neoplasm of biliary tract (disorder)", "Neoplasm of biliary tract (diagnosis)", "extrahepatic bile duct neoplasm - biliary tract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "biliary tract neoplasm", "shortest_name_length": 13}
{"curie": "UMLS:C3273230", "names": ["Intermediary Metabolism Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intermediary Metabolism Disorder", "shortest_name_length": 32}
{"curie": "UMLS:C1333981", "names": ["Mixed Embryonal/Fetal Hepatoblastoma", "Hepatoblastoma with Mixed Fetal and Embryonal Epithelial Differentiation", "Hepatoblastoma with Combined Fetal and Embryonal Epithelial Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatoblastoma with Combined Fetal and Embryonal Epithelial Differentiation", "shortest_name_length": 36}
{"curie": "MONDO:0024419", "names": ["enthesitis", "Enthesitis", "Enthesitis (disorder)", "enthesis inflammation", "inflammation of enthesis", "inflammatory enthesopathy", "Inflammation of sharpey fibres", "Inflammation of sharpey fibers"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "enthesitis", "shortest_name_length": 10}
{"curie": "MONDO:0017845", "names": ["SPAX", "spastic ataxia", "Spastic ataxia", "Spastic Ataxia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic ataxia", "shortest_name_length": 4}
{"curie": "UMLS:C4525736", "names": ["Stage I Colorectal Neuroendocrine Tumor", "Stage I Colorectal Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Colorectal Neuroendocrine Tumor AJCC v8", "shortest_name_length": 39}
{"curie": "UMLS:C0742468", "names": ["cns lesion", "CNS LESION", "cns lesions", "central lesion nervous system", "Central nervous system lesion", "Central Nervous System Lesion", "central lesions nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central nervous system lesion", "shortest_name_length": 10}
{"curie": "UMLS:C5556796", "names": ["Refractory Cervical Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Cervical Squamous Cell Carcinoma", "shortest_name_length": 43}
{"curie": "UMLS:C0016811", "names": ["Functional enuresis", "Nonorganic Enuresis", "functional enuresis", "Nonorganic enuresis", "Psychogenic enuresis", "Non-organic enuresis", "ENURESIS, FUNCTIONAL", "Enuresis;psychogenic", "psychogenic enuresis", "functional; enuresis", "enuresis; functional", "Enuresis (non-organic)", "Functional enuresis, NOS", "urine; incontinence, nonorganic origin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-organic enuresis", "shortest_name_length": 19}
{"curie": "MONDO:0013278", "names": ["LMPHM3", "LMPH1C", "LMPH1C, FORMERLY", "lymphatic malformation 3", "hereditary lymphedema IC", "LYMPHATIC MALFORMATION 3", "lymphedema, hereditary, IC", "lymphedema, hereditary, 1C", "GJC2 hereditary lymphedema", "lymphedema, hereditary, type 1C", "LYMPHEDEMA, HEREDITARY, IC, FORMERLY", "hereditary lymphedema caused by mutation in GJC2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphatic malformation 3", "shortest_name_length": 6}
{"curie": "UMLS:C1141936", "names": ["Purple glove syndrome", "Purple glove syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Purple glove syndrome", "shortest_name_length": 21}
{"curie": "MONDO:0007302", "names": ["CERVICAL HYPERTRICHOSIS WITH UNDERLYING KYPHOSCOLIOSIS", "Cervical Hypertrichosis with Underlying Kyphoscoliosis", "cervical hypertrichosis with underlying kyphoscoliosis", "hypertrichosis, posterior cervical, with underlying kyphoscoliosis", "Hypertrichosis, Posterior Cervical, with Underlying Kyphoscoliosis", "HYPERTRICHOSIS, POSTERIOR CERVICAL, WITH UNDERLYING KYPHOSCOLIOSIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical hypertrichosis with underlying kyphoscoliosis", "shortest_name_length": 54}
{"curie": "MONDO:0016685", "names": ["low-grade astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "low-grade astrocytoma", "shortest_name_length": 21}
{"curie": "MONDO:0007265", "names": ["Cfcs", "CFC1", "CFC syndrome", "cardiofaciocutaneous syndrome", "cardiofaciocutaneous syndrome 1", "BRAF cardiofaciocutaneous syndrome", "cardiofaciocutaneous syndrome type 1", "cardiofaciocutaneous syndrome caused by mutation in BRAF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiofaciocutaneous syndrome 1", "shortest_name_length": 4}
{"curie": "MONDO:0021639", "names": ["Grade 2 Glioma", "grade II glioma", "Grade II Glioma", "WHO Grade 2 Glioma", "WHO Grade II Glioma", "WHO grade II glioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "grade II glioma", "shortest_name_length": 14}
{"curie": "UMLS:C5206563", "names": ["Refractory Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Hepatocellular Carcinoma", "shortest_name_length": 35}
{"curie": "MONDO:0010646", "names": ["macular dystrophy, X-linked", "MACULAR DYSTROPHY, X-LINKED", "Macular Dystrophy, X-Linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macular dystrophy, X-linked", "shortest_name_length": 27}
{"curie": "MONDO:0007059", "names": ["Acrorenal Syndrome", "acrorenal syndrome", "ACRORENAL SYNDROME", "Acrorenal syndrome", "Acrorenal syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acrorenal syndrome", "shortest_name_length": 18}
{"curie": "UMLS:C2721578", "names": ["Pulmonary oil microembolism", "POME - Pulmonary oil microembolism", "Pulmonary oil microembolism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pulmonary oil microembolism", "shortest_name_length": 27}
{"curie": "UMLS:C0521169", "names": ["Wedge fracture", "FRACTURE COMPRESSION", "Compression Fracture", "fracture compression", "compression fracture", "Compression fracture", "Compression Fractures", "Fracture, compression", "Compression fractures", "compression fractures", "Fracture, Compression", "Fractures, Compression", "Compression fracture (disorder)", "Compression fracture (diagnosis)", "Compression fracture (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Compression fracture", "shortest_name_length": 14}
{"curie": "UMLS:C3272264", "names": ["SYNCOPE WITH INDUCIBLE VENTRICULAR TACHYCARDIA", "Syncope with Inducible Ventricular Tachycardia", "Syncope with Inducible Ventricular Tachycardia by EKG Finding", "Syncope with Inducible Ventricular Tachycardia by ECG Finding"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Syncope with Inducible Ventricular Tachycardia by ECG Finding", "shortest_name_length": 46}
{"curie": "UMLS:C5237458", "names": ["Recurrent T-MF", "Recurrent Transformed Mycosis Fungoides"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Transformed Mycosis Fungoides", "shortest_name_length": 14}
{"curie": "MONDO:0001977", "names": ["Ureter Lymphoma", "ureter lymphoma", "ureteral lymphoma", "Ureteral Lymphoma", "lymphoma of ureter", "Lymphoma of Ureter", "lymphoma of the ureter", "Lymphoma of the Ureter", "Primary Ureter Lymphoma", "primary ureter lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ureteral lymphoma", "shortest_name_length": 15}
{"curie": "UMLS:C5556834", "names": ["Hybrid Salivary Gland Tumor", "Hybrid Salivary Gland Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hybrid Salivary Gland Tumor", "shortest_name_length": 27}
{"curie": "UMLS:C0342406", "names": ["Pituitary bleeding", "pituitary hemorrhage", "Pituitary hemorrhage", "Pituitary Hemorrhage", "pituitary; hemorrhage", "pituitary haemorrhage", "Pituitary haemorrhage", "hemorrhage; pituitary", "Pituitary hemorrhage (disorder)", "Pituitary hemorrhage (diagnosis)", "intracerebral hemorrhage pituitary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pituitary hemorrhage", "shortest_name_length": 18}
{"curie": "UMLS:C3898463", "names": ["Masaoka Stage II", "Masaoka-Koga Stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Masaoka-Koga Stage II", "shortest_name_length": 16}
{"curie": "MONDO:0006112", "names": ["inflammatory myofibroblastic bladder tumor", "Bladder Inflammatory Myofibroblastic Tumor", "bladder inflammatory myofibroblastic tumor", "inflammatory myofibroblastic tumor of bladder", "Inflammatory Myofibroblastic Tumor of Bladder", "bladder inflammatory myofibroblastic neoplasm", "Bladder Inflammatory Myofibroblastic Neoplasm", "Inflammatory Myofibroblastic Neoplasm of Bladder", "inflammatory myofibroblastic neoplasm of bladder", "inflammatory myofibroblastic tumor of the bladder", "Inflammatory Myofibroblastic Tumor of the Bladder", "urinary bladder inflammatory myofibroblastic tumor", "Urinary Bladder Inflammatory Myofibroblastic Tumor", "inflammatory myofibroblastic neoplasm of the bladder", "Inflammatory Myofibroblastic Neoplasm of the Bladder", "inflammatory myofibroblastic tumor of urinary bladder", "urinary bladder inflammatory myofibroblastic neoplasm", "Inflammatory Myofibroblastic Tumor of Urinary Bladder", "Urinary Bladder Inflammatory Myofibroblastic Neoplasm", "inflammatory myofibroblastic neoplasm of urinary bladder", "Inflammatory Myofibroblastic Neoplasm of Urinary Bladder", "Inflammatory Myofibroblastic Tumor of the Urinary Bladder", "inflammatory myofibroblastic tumor of the urinary bladder", "inflammatory myofibroblastic neoplasm of the urinary bladder", "Inflammatory Myofibroblastic Neoplasm of the Urinary Bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder inflammatory myofibroblastic tumor", "shortest_name_length": 42}
{"curie": "UMLS:C3900106", "names": ["B Acute Lymphoblastic Leukemia with t(9;22)(q34.1;q11.2); BCR-ABL1", "Adult B Acute Lymphoblastic Leukemia with t(9;22)(q34;q11.2); BCR-ABL1", "Adult B Acute Lymphoblastic Leukemia with t(9;22)(q34.1;q11.2); BCR-ABL1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult B Acute Lymphoblastic Leukemia with t(9;22)(q34.1;q11.2); BCR-ABL1", "shortest_name_length": 66}
{"curie": "UMLS:C4087264", "names": ["Depersonalisation/derealisation disorder", "Depersonalization/derealization disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Depersonalization/derealization disorder", "shortest_name_length": 40}
{"curie": "MONDO:0013636", "names": ["PBC4", "biliary cirrhosis, primary, 4", "primary biliary cholangitis 4", "BILIARY CIRRHOSIS, PRIMARY, 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary biliary cholangitis 4", "shortest_name_length": 4}
{"curie": "MONDO:0001745", "names": ["subserous uterine fibroid", "Subserous uterine fibroid", "Subserous uterine leiomyoma", "subserous uterine leiomyoma", "uterus; leiomyoma, subserosal", "leiomyoma; uterus, subserosal", "subserous leiomyoma of uterus", "Subserous leiomyoma of uterus", "Subserosal leiomyoma of uterus", "Subserous leiomyoma of uterus (disorder)", "subserous leiomyoma of uterus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subserous uterine fibroid", "shortest_name_length": 25}
{"curie": "MONDO:0014168", "names": ["IMD8", "IMMUNODEFICIENCY 8", "immunodeficiency 8", "coronin-1A deficiency", "immunodeficiency type 8", "SCID due to CORO1A deficiency", "SCID due to coronin-1A deficiency", "Severe combined immunodeficiency due to CORO1A deficiency", "severe combined immunodeficiency due to CORO1A deficiency", "Severe combined immunodeficiency due to coronin 1A deficiency", "severe combined immunodeficiency due to coronin-1A deficiency", "Severe combined immunodeficiency due to coronin-1A deficiency", "Severe combined immunodeficiency due to coronin 1A deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe combined immunodeficiency due to CORO1A deficiency", "shortest_name_length": 4}
{"curie": "UMLS:C5555297", "names": ["Current HIV Infection", "Current_HIV_infection", "Current Human Immunodeficiency Virus Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Current HIV Infection", "shortest_name_length": 21}
{"curie": "MONDO:0034109", "names": ["MYOFTA", "congenital myopathy 14", "Congenital myopathy with type II fiber atrophy", "Congenital myopathy with type II fibre atrophy", "Congenital myopathy with fast-twitch fiber atrophy", "Congenital myopathy with fast-twitch fibre atrophy", "Congenital myopathy with type 2 muscle fiber atrophy", "Congenital myopathy with type 2 muscle fibre atrophy", "Congenital myopathy with reduced type 2 muscle fibers", "Congenital myopathy with reduced type 2 muscle fibres", "congenital myopathy with reduced type 2 muscle fibers", "Congenital myopathy with reduced type II muscle fibers", "Congenital myopathy with reduced type II muscle fibres", "MYOPATHY, CONGENITAL, WITH FAST-TWITCH (TYPE II) FIBER ATROPHY", "myopathy, congenital, with fast-twitch (type II) fiber atrophy", "Congenital myopathy with reduced type 2 muscle fibers (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myopathy with reduced type 2 muscle fibers", "shortest_name_length": 6}
{"curie": "UMLS:C0853339", "names": ["Reperfusion arrhythmia", "reperfusion arrhythmia", "reperfusion arrhythmias", "Reperfusion arrhythmias"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reperfusion arrhythmia", "shortest_name_length": 22}
{"curie": "MONDO:0035160", "names": ["progressive myoclonic epilepsy with neuroserpin inclusion bodies", "early onset familial encephalopathy with neuroserpin inclusion bodies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive myoclonic epilepsy with neuroserpin inclusion bodies", "shortest_name_length": 64}
{"curie": "MONDO:0002537", "names": ["invert papilloma", "Inverted Papilloma", "Inverted papilloma", "inverted papilloma", "Papilloma, Inverted", "Inverted Papillomas", "inverted papillomas", "inverting papilloma", "Papillomas, Inverted", "Benign inverted papilloma", "inverted papilloma, squamous cell", "Inverted papilloma, squamous cell", "Benign inverted papilloma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inverted papilloma", "shortest_name_length": 16}
{"curie": "MONDO:0021582", "names": ["LENTIGO", "lentigo", "Lentigo", "lentigos", "Lentigos", "Lentigines", "LENTIGINES", "lentigines", "Lentiginoses", "Lentiginosis", "Lentigo, NOS", "lentiginosis", "lentigo (diagnosis)", "Lentiginosis (disorder)", "Lentigo (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lentigo", "shortest_name_length": 7}
{"curie": "MONDO:8000006", "names": ["WHIM", "WILM", "WHIMS", "WHIMS1", "WHIM Syndrome", "WHIM syndrome", "WHIM SYNDROME 1", "WHIM syndrome 1", "myelokathexis, isolated", "Warts-infections-leukopenia-myelokatexis syndrome", "Warts, hypogammaglobulinemia, infections, and myelokathexis", "warts, hypogammaglobulinemia, infections, and myelokathexis", "Warts, hypogammaglobulinaemia, infections, and myelokathexis", "warts-hypogammaglobulinemia-infections-myelokathexis syndrome", "Warts-hypogammaglobulinemia-infections-myelokathexis syndrome", "WHIM - Warts, hypogammaglobulinemia, infections and myelokathexis", "WHIM - Warts, hypogammaglobulinaemia, infections and myelokathexis", "Warts, hypogammaglobulinemia, infections, and myelokathexis syndrome", "Warts, Hypogammaglobulinemia, Infections, and Myelokathexis Syndrome", "WARTS, HYPOGAMMAGLOBULINEMIA, INFECTIONS, AND MYELOKATHEXIS SYNDROME 1", "Warts, hypogammaglobulinemia, infections, and myelokathexis (disorder)", "warts, hypogammaglobulinemia, infections, and myelokathexis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "WHIM syndrome 1", "shortest_name_length": 4}
{"curie": "UMLS:C5238706", "names": ["Gestational Complication", "Gestational Complications"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gestational Complication", "shortest_name_length": 24}
{"curie": "MONDO:0007100", "names": ["FAP", "paramyloidosis", "TTR amyloidosis", "ATTR amyloidosis", "ATTRm amyloidosis", "AF type amyloidosis", "ATTRV30M amyloidosis", "TTR amyloid neuropathy", "PARAMYLOIDOSIS, FAMILIAL", "TRANSTHYRETIN AMYLOIDOSIS", "Transthyretin Amyloidosis", "transthyretin amyloidosis", "familial amyloid neuropathy", "Familial Amyloid Neuropathy", "Corino de Andrade's disease", "Neuropathy, Familial Amyloid", "ATTRV30M-related amyloidosis", "Amyloid Neuropathy, Familial", "Amyloid neuropathy, familial", "Familial Amyloid Neuropathies", "Neuropathies, Familial Amyloid", "Amyloid Neuropathies, Familial", "amyloid Neuropathies, familial", "Familial amyloid polyneuropathy", "familial amyloid polyneuropathy", "Familial Amyloid Polyneuropathy", "amyloid polyneuropathy, familial", "transthyretin amyloid neuropathy", "Polyneuropathy, Familial Amyloid", "Familial neuropathic amyloidosis", "AMYLOID POLYNEUROPATHY, FAMILIAL", "Amyloid Polyneuropathy, Familial", "amyloidosis transthyretin related", "amyloid familial polyneuropathies", "Familial Amyloid Polyneuropathies", "Hereditary neuropathic amyloidosis", "Familial transthyretin amyloidosis", "Amyloid Polyneuropathies, Familial", "Hereditary Neuropathic Amyloidosis", "Polyneuropathies, Familial Amyloid", "Hereditary Neuropathic Amyloidoses", "familial transthyretin amyloidosis", "Neuropathic Amyloidoses, Hereditary", "Amyloidoses, Hereditary Neuropathic", "Amyloidosis, Hereditary Neuropathic", "Neuropathic Amyloidosis, Hereditary", "transthyretin amyloid polyneuropathy", "AMYLOIDOSIS, HEREDITARY, NEUROPATHIC", "Familial polyneuropathic amyloidosis", "Familial amyloid polyneuropathy, NOS", "hereditary transthyretin amyloidosis", "Neuropathic heredofamilial amyloidosis", "amyloidosis heredofamilial neuropathic", "familial amyloid polyneuropathy type I", "neuropathic; heredofamilial amyloidosis", "neuropathic; amyloidosis, heredofamilial", "heredofamilial; amyloidosis, neuropathic", "amyloidosis; neuropathic, heredofamilial", "amyloidosis; heredofamilial, neuropathic", "Familial amyloid polyneuropathy (disorder)", "Familial Transthyretin Cardiac Amyloidosis", "transthyretin-related hereditary amyloidosis", "AMYLOID CARDIOMYOPATHY, TRANSTHYRETIN-RELATED", "Hereditary neuropathic amyloidosis (Rukavina)", "amyloid cardiomyopathy, transthyretin-related", "hereditary amyloidosis, transthyretin-related", "Hereditary Amyloidosis, Transthyretin-Related", "HEREDITARY AMYLOIDOSIS, TRANSTHYRETIN-RELATED", "amyloidosis, hereditary, transthyretin-related", "Amyloidosis, Hereditary, Transthyretin-Related", "Amyloidosis, hereditary, transthyretin-related", "AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED", "amyloidosis heredofamilial neuropathic (diagnosis)", "amyloidosis, leptomeningeal, transthyretin-related", "AMYLOIDOSIS, LEPTOMENINGEAL, TRANSTHYRETIN-RELATED", "familial amyloid polyneuropathy, Portuguese-Swedish-Japanese type", "familial amyloid polyneuropathy type I (Portuguese-Swedish-Japanese type)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial amyloid neuropathy", "shortest_name_length": 3}
{"curie": "UMLS:C5420649", "names": ["Metastatic Vulvar Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Vulvar Squamous Cell Carcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0014137", "names": ["CPPB2", "central precocious puberty 2", "PRECOCIOUS PUBERTY, CENTRAL, 2", "precocious puberty, central, 2", "MKRN3 central precocious puberty", "precocious puberty, central, type 2", "central precocious puberty caused by mutation in MKRN3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "precocious puberty, central, 2", "shortest_name_length": 5}
{"curie": "UMLS:C4727839", "names": ["Locally Advanced Head and Neck Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Head and Neck Carcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0030437", "names": ["CDG2W", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIw", "congenital disorder of glycosylation, type IIw"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital disorder of glycosylation, type IIw", "shortest_name_length": 5}
{"curie": "MONDO:0002958", "names": ["signet ring basal cell carcinoma", "signet Ring cell basal cell carcinoma", "Signet Ring Cell Basal Cell Carcinoma", "skin signet ring cell basal cell carcinoma", "Skin Signet-Ring Cell Basal Cell Carcinoma", "skin signet Ring cell basal cell carcinoma", "Skin Signet Ring Cell Basal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "signet ring basal cell carcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C2828252", "names": ["Stage IVB Lip and Oral Cavity Cancer", "stage IVB lip and oral cavity cancer", "Stage IVB Lip and Oral Cavity Cancer AJCC v6", "Stage IVB Lip and Oral Cavity Cancer AJCC v7", "Stage IVB Lip and Oral Cavity Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Lip and Oral Cavity Cancer AJCC v6 and v7", "shortest_name_length": 36}
{"curie": "UMLS:C1333946", "names": ["Heart Myeloid Sarcoma", "Cardiac Myeloid Sarcoma", "Heart Extramedullary Myeloid Tumor", "Cardiac Extramedullary Myeloid Tumor", "Heart Extramedullary Myeloid Neoplasm", "Extramedullary Myeloid Tumor of Heart", "Cardiac Extramedullary Myeloid Neoplasm", "Extramedullary Myeloid Neoplasm of Heart", "Extramedullary Myeloid Tumor of the Heart", "Extramedullary Myeloid Neoplasm of the Heart"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiac Myeloid Sarcoma", "shortest_name_length": 21}
{"curie": "MONDO:0017570", "names": ["LAD", "leukocyte adhesion deficiency", "Leukocyte adhesion deficiency", "Leukocyte Adhesion Deficiency", "Leukocyte-Adhesion Deficiency Syndrome", "Leukocyte Adhesion Deficiency Syndrome", "Leukocyte-Adhesion Deficiency Syndromes", "Deficiency Syndrome, Leukocyte-Adhesion", "Deficiency Syndrome, Leukocyte Adhesion", "Congenital leukocyte adherence deficiency", "congenital leukocyte adherence deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukocyte adhesion deficiency", "shortest_name_length": 3}
{"curie": "UMLS:C0014860", "names": ["Perforation esophagus", "PERFORATION ESOPHAGUS", "esophagus perforation", "ESOPHAGUS PERFORATION", "perforation esophagus", "perforation; esophagus", "esophagus; perforation", "esophageal perforation", "Perforation oesophagus", "Esophageal perforation", "Esophageal Perforation", "ESOPHAGUS, PERFORATION", "ESOPHAGEAL PERFORATION", "oesophageal perforation", "Perforation, Esophageal", "OESOPHAGEAL PERFORATION", "Oesophageal perforation", "Esophageal Perforations", "Perforation of Esophagus", "perforation of esophagus", "Perforation Of Esophagus", "Perforations, Esophageal", "Perforation of esophagus", "Perforation of oesophagus", "esophageal perforation (diagnosis)", "Perforation of esophagus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Perforation", "shortest_name_length": 21}
{"curie": "MONDO:0006624", "names": ["OAB", "urge syndrome", "overactive bladder", "urgency-frequency syndrome", "overactive bladder syndrome", "Urinary Bladder, Overactive", "overactive bladder (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "overactive bladder", "shortest_name_length": 3}
{"curie": "MONDO:0012432", "names": ["JBTS5", "Joubert syndrome 5", "JOUBERT SYNDROME 5", "Joubert syndrome type 5", "CEP290 Joubert syndrome", "Joubert syndrome caused by mutation in CEP290"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome 5", "shortest_name_length": 5}
{"curie": "UMLS:C0280355", "names": ["Stage III Mouth Verrucous Carcinoma", "Stage III Oral Cavity Verrucous Cancer", "Stage III Verrucous Carcinoma of Mouth", "Stage III Oral Cavity Verrucous Carcinoma", "Stage III Verrucous Carcinoma of the Mouth", "oral cavity verrucous carcinoma, stage III", "Stage III Verrucous Carcinoma of Oral Cavity", "Verrucous carcinoma of the oral cavity stage III", "stage III verrucous carcinoma of the oral cavity", "Stage III Verrucous Carcinoma of the Oral Cavity", "verrucous carcinoma of the oral cavity, stage III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Verrucous carcinoma of the oral cavity stage III", "shortest_name_length": 35}
{"curie": "MONDO:0006805", "names": ["rest angina", "rest; angina", "Angina at Rest", "Angina at rest", "angina at rest", "Unstable Angina", "Angina;unstable", "Angina unstable", "angina unstable", "ANGINA UNSTABLE", "Unstable angina", "UNSTABLE ANGINA", "unstable angina", "unstable; angina", "Angina, Unstable", "crescendo angina", "Crescendo angina", "Worsening angina", "worsening angina", "CRESCENDO ANGINA", "Unstable Anginas", "crescendo; angina", "Anginas, Unstable", "syndrome; coronary", "coronary; syndrome", "impending infarction", "Infarction;impending", "preinfarction angina", "Impending infarction", "Preinfarction Angina", "Preinfarction angina", "Angina, Preinfarction", "Preinfarction Anginas", "PREINFARCTION SYNDROME", "Preinfarction syndrome", "Anginas, Preinfarction", "pre-infarction syndrome", "preinfarction; syndrome", "syndrome; preinfarction", "Pre-infarction syndrome", "preinfarctional; angina", "Unstable Angina Pectori", "Pre infarction syndrome", "Angina pectoris unstable", "angina pectoris; at rest", "UNSTABLE ANGINA PECTORIS", "Angina Pectori, Unstable", "unstable angina pectoris", "Unstable Angina Pectoris", "Angina pectoris, unstable", "Angina Pectoris, Unstable", "angina pectoris; unstable", "crescendo angina pectoris", "anginal chest pain at rest", "Anginal chest pain at rest", "angina pectoris; crescendo", "Angina pectoris, crescendo", "Intermediate coronary syndrome", "intermediate coronary syndrome", "intermediate coronary; syndrome", "syndrome; intermediate coronary", "Impending infarction (disorder)", "Impending infarction (diagnosis)", "Myocardial preinfarction syndrome", "Preinfarction syndrome (disorder)", "Myocardial Preinfarction Syndrome", "Myocardial Preinfarction Syndromes", "Syndrome, Myocardial Preinfarction", "Preinfarction Syndrome, Myocardial", "Preinfarction Syndromes, Myocardial", "Syndromes, Myocardial Preinfarction", "unstable angina pectoris (diagnosis)", "Intermediate ischemic heart syndrome", "crescendo angina pectoris (diagnosis)", "myocardial ischemia impending infarction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intermediate coronary syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0014866", "names": ["CMT2T", "AR-CMT2T", "DNAJB2-related CMT2", "Charcot-Marie-Tooth disease type 2T", "Charcot-Marie-Tooth neuropathy type 2T", "Charcot-Marie-Tooth neuropathy, type 2T", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2T", "Charcot-Marie-Tooth disease axonal type 2T", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2T", "Charcot-Marie-Tooth disease, axonal, type 2T", "Charcot-Marie-Tooth disease type 2T (disorder)", "DNAJB2-related Charcot-Marie-Tooth disease type 2", "autosomal recessive axonal Charcot-Marie-Tooth disease type 2T", "Autosomal recessive axonal Charcot-Marie-Tooth disease type 2T", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2T", "Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2T"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease axonal type 2T", "shortest_name_length": 5}
{"curie": "UMLS:C0159626", "names": ["RIB FRACTURE MULTIPLE CLOSED", "Closed fracture multiple ribs", "Closed fracture of multiple ribs", "closed fracture of multiple ribs", "Closed fracture of multiple ribs, NOS", "Closed Fracture of Ribs, Multiple Sites", "Closed fracture of multiple ribs (disorder)", "closed fracture of multiple ribs (diagnosis)", "Closed fracture of multiple ribs, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Closed fracture of multiple ribs", "shortest_name_length": 28}
{"curie": "UMLS:C4725702", "names": ["HHV8-Related Lymphoproliferative Disorder", "HHV8-Associated Lymphoproliferative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HHV8-Related Lymphoproliferative Disorder", "shortest_name_length": 41}
{"curie": "UMLS:C4528550", "names": ["Stage 0 Breast Cancer", "Anatomic Stage 0 Breast Cancer AJCC v8", "Anatomic Stage 0 Breast Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anatomic Stage 0 Breast Cancer AJCC v8", "shortest_name_length": 21}
{"curie": "UMLS:C4683548", "names": ["Stage III Adrenal Gland Pheochromocytoma and Sympathetic Paraganglioma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Adrenal Gland Pheochromocytoma and Sympathetic Paraganglioma AJCC v8", "shortest_name_length": 78}
{"curie": "MONDO:0006140", "names": ["Cervical Adenoma Malignum", "cervical adenoma malignum", "Cervical Mucinous Adenocarcinoma, Gastric Type", "HPV-Independent Cervical Adenocarcinoma, Gastric-Type", "Cervical Mucinous Adenocarcinoma, Minimal Deviation Type", "cervical mucinous adenocarcinoma, minimal deviation type", "Cervical Mucinous Adenocarcinoma, Minimal Deviation Variant", "cervical mucinous adenocarcinoma, minimal deviation variant", "Human Papillomavirus-Independent Cervical Adenocarcinoma, Gastric-Type", "Human Papillomavirus-Independent Cervical Adenocarcinoma, Gastric Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical mucinous adenocarcinoma, minimal deviation variant", "shortest_name_length": 25}
{"curie": "UMLS:C0234943", "names": ["ANESTHESIA APPLICATION SITE", "APPLICATION SITE ANESTHESIA", "Anesthesia application site", "Application site anesthesia", "APPLICATION SITE ANAESTHESIA", "Application site anaesthesia", "Anaesthesia application site", "Application site anesthesia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Application site anesthesia", "shortest_name_length": 27}
{"curie": "UMLS:C1332623", "names": ["Metastatic Breast Cancer in the Bone", "Breast Carcinoma Metastatic in the Bone", "Breast Carcinoma Metastatic to the Bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Carcinoma Metastatic in the Bone", "shortest_name_length": 36}
{"curie": "UMLS:C0039338", "names": ["Taste Disorder", "Taste disorder", "taste disorder", "disorder taste", "disorders taste", "Taste Disorders", "taste disorders", "Taste disorders", "Disorder of taste", "Disorder of taste (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Taste Disorders", "shortest_name_length": 14}
{"curie": "MONDO:0004219", "names": ["polyvesicular vitelline pattern testicular yolk sac tumor", "testicular yolk Sac tumor, polyvesicular vitelline pattern", "Testicular Yolk Sac Tumor, Polyvesicular Vitelline Pattern"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyvesicular vitelline pattern testicular yolk sac tumor", "shortest_name_length": 57}
{"curie": "MONDO:0023091", "names": ["esophageal atresia coloboma talipes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophageal atresia coloboma talipes", "shortest_name_length": 35}
{"curie": "MONDO:0006830", "names": ["kraurosis penis", "Kraurosis Penis", "penis; kraurosis", "kraurosis; penis", "leukoplakia penis", "kraurosis of penis", "penis; leukoplakia", "leukoplakia; penis", "Kraurosis of penis", "Penile Leukoplakia", "penile leukoplakia", "Leukoplakia of penis", "Leukoplakia of Penis", "leukoplakia of penis", "Leucoplakia of penis", "Leukoplakia of the Penis", "leukoplakia of the penis", "Balanitis xerotica obliterans", "Balanitis Xerotica Obliterans", "Leukoplakia of penis (disorder)", "leukoplakia of penis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukoplakia of penis", "shortest_name_length": 15}
{"curie": "MONDO:0018475", "names": ["PRKAR1B-related neurodegenerative dementia with intermediate filaments"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PRKAR1B-related neurodegenerative dementia with intermediate filaments", "shortest_name_length": 70}
{"curie": "UMLS:C3683846", "names": ["17p- Syndrome", "Partial Monosomy 17p", "Deletion 17p Syndrome", "Interstitial deletion 17p", "Chromosome 17p Deletion Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chromosome 17p Deletion Syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0010591", "names": ["Fingerprint Body Myopathy", "FINGERPRINT BODY MYOPATHY", "Fingerprint body myopathy", "fingerprint body myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fingerprint body myopathy", "shortest_name_length": 25}
{"curie": "UMLS:C3272434", "names": ["Ampullary Low Grade Intraepithelial Neoplasia", "Ampullary Noninvasive Pancreatobiliary Papillary Neoplasm with Low Grade Dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ampullary Noninvasive Pancreatobiliary Papillary Neoplasm with Low Grade Dysplasia", "shortest_name_length": 45}
{"curie": "UMLS:C5206560", "names": ["Recurrent Colorectal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Colorectal Adenocarcinoma", "shortest_name_length": 35}
{"curie": "MONDO:0000463", "names": ["UFS", "UFS1", "ochoa syndrome", "OCHOA SYNDROME", "Ochoa syndrome", "urofacial syndrome", "Urofacial syndrome", "UROFACIAL SYNDROME", "UROFACIAL SYNDROME 1", "Ochoa syndrome (disorder)", "urofacial Ochoa's syndrome", "Urofacial Ochoa's syndrome", "Hydronephrosis-Inverted Smile", "Inverted Smile-Neurogenic Bladder", "hydronephrosis-inverted smile syndrome", "Hydronephrosis-inverted smile syndrome", "inverted smile-neurogenic bladder syndrome", "Inverted smile-neurogenic bladder syndrome", "Inverted smile and occult neuropathic bladder", "inverted smile and occult neuropathic bladder", "INVERTED SMILE AND OCCULT NEUROPATHIC BLADDER", "Hydronephrosis with peculiar facial expression", "hydronephrosis with peculiar facial expression", "HYDRONEPHROSIS WITH PECULIAR FACIAL EXPRESSION", "Partial facial palsy with urinary abnormalities", "partial facial palsy with urinary abnormalities", "FACIAL PALSY, PARTIAL, WITH URINARY ABNORMALITIES", "Facial Palsy, Partial, With Urinary Abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ochoa syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C4725614", "names": ["Refractory Endometrial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Endometrial Carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0000481", "names": ["Loxia", "WRYNECK", "Wryneck", "wryneck", "Wry neck", "wry neck", "Head tilt", "Torticollis", "TORTICOLLIS", "retrocollis", "torticollis", "Torticollis, NOS", "neck contracture", "Neck contractures", "Cervical Dystonia", "cervical dystonia", "Cervical dystonia", "dystonia cervical", "Cervical Dystonias", "Dystonia, Cervical", "cervical dystonias", "Contracture of neck", "Dystonias, Cervical", "contracture of neck", "Spasmodic torticollis", "torticollis spasmodic", "Spasmodic Torticollis", "spasmodic torticollis", "spasmodic; torticollis", "Torticollis (disorder)", "torticollis; spasmodic", "Torticollis, Spasmodic", "torticollis unspecified", "torticollis (diagnosis)", "Torticollis, unspecified", "Contracture of neck, NOS", "contracture of neck (diagnosis)", "Spasmodic torticollis (disorder)", "spasmodic torticollis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical dystonia", "shortest_name_length": 5}
{"curie": "UMLS:C4744713", "names": ["Locally Advanced Prostate Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Prostate Carcinoma", "shortest_name_length": 35}
{"curie": "MONDO:0018124", "names": ["OO", "TIO", "OOM", "osteomalacia oncogenic", "Oncogenic osteomalacia", "Oncogenic Osteomalacia", "Tumor-induced osteomalacia", "tumor-induced osteomalacia", "Tumour-induced osteomalacia", "Osteomalacia due to neoplasm", "osteomalacia oncogenic (diagnosis)", "Osteomalacia due to neoplastic disease", "Oncogenic hypophosphatemic osteomalacia", "Osteomalacia due to neoplastic disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oncogenic osteomalacia", "shortest_name_length": 2}
{"curie": "UMLS:C0302810", "names": ["UREMIC SYNDROME", "uremia syndrome", "SYNDROME UREMIC", "Uremic syndrome", "uremic syndrome", "Uremia syndrome", "Syndrome uremic", "syndrome uraemic", "URAEMIC SYNDROME", "uremia; syndrome", "syndrome; uremia", "Uraemic syndrome", "Syndrome uraemic", "uraemic syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uremia syndrome", "shortest_name_length": 15}
{"curie": "UMLS:C1335997", "names": ["Small Intestinal High-Grade Dysplasia", "Small Intestinal High Grade Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Intestinal High Grade Intraepithelial Neoplasia", "shortest_name_length": 37}
{"curie": "MONDO:0006244", "names": ["HER2+ breast cancer", "HER2 positive breast cancer", "HER2-positive breast cancer", "HER2 Positive Breast Cancer", "HER2 Positive breast cancer", "HER2 positive breast carcinoma", "HER2 Positive Breast Carcinoma", "HER2-Positive Breast Carcinoma", "HER2/neu-positive breast cancer", "HER2-positive carcinoma of breast", "HER2 Overexpressing Breast Carcinoma", "Her2-receptor positive breast cancer", "HER2 Overexpressing breast carcinoma", "breast neoplasm malignant her2-positive", "HER-2 positive malignant carcinoma of breast", "HER2 Overexpressing Subtype of Breast Carcinoma", "HER2 Overexpressing subtype of breast carcinoma", "ERBB2 Overexpressing Subtype of Breast Carcinoma", "ERBB2 Overexpressing subtype of breast carcinoma", "HER-2 positive malignant carcinoma of breast (diagnosis)", "Human epidermal growth factor 2 positive carcinoma of breast", "Human epidermal growth factor 2 positive carcinoma of breast (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HER2 positive breast carcinoma", "shortest_name_length": 19}
{"curie": "UMLS:C0686106", "names": ["anal neoplasm malignant secondary", "Secondary malignant neoplasm of anus", "Metastatic malignant neoplasm of anus", "Metastatic malignant neoplasm to anus", "Metastatic Malignant Neoplasm to the Anus", "Metastatic Malignant Neoplasm in the Anus", "Secondary malignant neoplasm of anus (diagnosis)", "Metastatic malignant neoplasm to anus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to anus", "shortest_name_length": 33}
{"curie": "UMLS:C4682693", "names": ["stage 0is penile cancer", "Stage 0is Penile Cancer", "Stage 0is Penile Cancer AJCC v8", "stage 0is penile cancer AJCC v8", "Stage 0is Penile Squamous Cell Carcinoma AJCC v8", "stage 0is penile squamous cell carcinoma AJCC v8", "Stage 0is Squamous Cell Carcinoma of the Penis AJCC v8", "stage 0is squamous cell carcinoma of the penis AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0is Penile Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "MONDO:0006320", "names": ["non-cutaneous melanoma", "Non-Cutaneous Melanoma", "extracutaneous melanoma", "Extracutaneous Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-cutaneous melanoma", "shortest_name_length": 22}
{"curie": "MONDO:0024660", "names": ["Tubular adenoma", "ADENOMA TUBULAR", "tubular adenoma", "adenoma tubular", "Tubular Adenoma", "adenomas tubular", "Tubular adenoma NOS", "Tubular adenoma, NOS", "GI Tract Tubular Adenoma", "Tubular adenoma (disorder)", "ADENOMA, TUBULAR CELL, BENIGN", "adenoma, tubular cell, benign", "Gastrointestinal Tract Tubular Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tubular adenoma", "shortest_name_length": 15}
{"curie": "MONDO:0004604", "names": ["LRCHL", "lymphocyte rich Hodgkin lymphoma", "Lymphocyte Rich Hodgkin Lymphoma", "Lymphocyte-rich Hodgkin lymphoma", "Lymphocyte Rich Hodgkin's disease", "lymphocyte rich Hodgkin's disease", "Hodgkin Lymphoma, Lymphocyte-Rich", "Hodgkin lymphoma, lymphocyte-rich", "Lymphocyte Rich Hodgkin's Disease", "Hodgkin; lymphocytic predominance", "Lymphocyte Rich Hodgkin's Lymphoma", "lymphocyte rich Hodgkin's lymphoma", "lymphocyte predominant Hodgkin lymphoma", "Lymphocyte-Rich Classic Hodgkin Lymphoma", "lymphocyte-rich Classic Hodgkin lymphoma", "Hodgkin lymphoma, lymphocyte predominant", "Lymphocyte-rich classical Hodgkin lymphoma", "Lymphocyte Rich Classical Hodgkin Lymphoma", "lymphocyte-rich classical Hodgkin lymphoma", "lymphocyte rich classical Hodgkin lymphoma", "Lymphocyte-Rich Classical Hodgkin Lymphoma", "Hodgkin's disease, lymphocyte predominance", "lymphocyte rich classical Hodgkin's disease", "Classical Hodgkin lymphoma, lymphocyte-rich", "Lymphocyte Rich Classical Hodgkin's Disease", "Hodgkin's disease, lymphocytic predominance", "disease; Hodgkin's, lymphocytic predominance", "Hodgkin lymphoma, lymphocyte-rich (disorder)", "lymphocyte rich classical Hodgkin's lymphoma", "lymphocyte-rich classical Hodgkin's lymphoma", "Lymphocyte-Rich Classical Hodgkin's Lymphoma", "Lymphocyte Rich Classical Hodgkin's Lymphoma", "Hodgkin lymphoma, lymphocyte-rich (clinical)", "Hodgkin; lymphocytic-histiocytic predominance", "classic Hodgkin lymphoma, lymphocyte-rich type", "Hodgkin's disease, lymphocytic predominance NOS", "Hodgkin's disease with lymphocytic predominance", "Hodgkin's disease, lymphocyte predominance [obs]", "Hodgkin's disease, lymphocytic predominance, NOS", "lymphocyte predominant Hodgkin lymphoma (diagnosis)", "Hodgkin lymphoma, lymphocytic-histiocytic predominance", "Hodgkin's disease, lymphocytic-histiocytic predominance", "Hodgkin's lymphoma, lymphocytic-histiocytic predominance", "disease; Hodgkin's, lymphocytic-histiocytic predominance", "Hodgkin lymphoma with lymphocytic-histiocytic predominance", "Hodgkin lymphoma, lymphocyte-rich (morphologic abnormality)", "Hodgkin's disease lymphocyte predominance type stage unspecified", "Hodgkin lymphoma with lymphocytic-histiocytic predominance (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's lymphoma, lymphocytic-histiocytic predominance", "shortest_name_length": 5}
{"curie": "UMLS:C0347065", "names": ["Local Tumor Spread", "Local tumor spread", "Local Tumour Spread", "Local tumour spread", "Local tumor spread (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Local tumor spread", "shortest_name_length": 18}
{"curie": "UMLS:C4684880", "names": ["Advanced Bile Duct Cancer", "Advanced Bile Duct Carcinoma", "Advanced Biliary Tract Cancer", "Advanced Biliary Tract Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Bile Duct Carcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0013282", "names": ["A1AD", "AATD", "A1ATD", "A-1ATD", "AAT deficiency", "A1AT deficiency", "Alpha-1 Antitrypsin", "Deficiency;A1 antitrypsin", "Alpha 1-Antitrypsin Disease", "Alpha1-antitrypsin deficiency", "ALPHA-1 ANTITRYPSIN DEFICIENCY", "alpha-1-Antitrypsin deficiency", "ALPHA-1-ANTITRYPSIN DEFICIENCY", "alpha 1 antitrypsin deficiency", "alpha 1-Antitrypsin Deficiency", "1 alpha antitrypsin deficiency", "alpha 1 Antitrypsin Deficiency", "Alpha 1-antitrypsin deficiency", "alpha 1-antitrypsin deficiency", "Alpha-1 antitrypsin deficiency", "alpha-1 antitrypsin deficiency", "ALPHA 1 ANTITRYPSIN DEFICIENCY", "Alpha-1-antitrypsin deficiency", "Alpha-1 Antitrypsin Deficiency", "alpha-1-antitrypsin deficiency", "Alpha 1 antitrypsin deficiency", "Alpha-1-Antitrypsin Deficiency", "ALPHA-1-antitrypsin deficiency", "alpha-1 anti-trypsin deficiency", "deficiency; alpha-1-antitrypsin", "Deficiency, alpha 1-Antitrypsin", "emphysema due to AAT deficiency", "alpha-1-antitrypsin; deficiency", "Alpha-1 anti-trypsin deficiency", "alpha 1-Antitrypsin Deficiencies", "Deficiencies, alpha 1-Antitrypsin", "alpha-1-Proteinase inhibitor deficiency", "Alpha-1 proteinase inhibitor deficiency", "Alpha-1-proteinase inhibitor deficiency", "Alpha-1-antitrypsin deficiency (disorder)", "deficiency in Alpa-1-proteinase inhibitor", "alpha 1-antitrypsin deficiency (diagnosis)", "emphysema-cirrhosis, due to AAT deficiency", "hemorrhagic diathesis due to antithrombin pittsburgh"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alpha 1-antitrypsin deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0010576", "names": ["DFN3", "DFNX2", "NANCE DEAFNESS", "Nance deafness", "gusher syndrome", "perceptive deafness", "X-linked deafness 2", "DEAFNESS, X-LINKED 2", "sensory hearing loss", "central hearing loss", "Deafness, X-Linked 2", "deafness, X-linked 2", "sensorineural deafness", "high frequency deafness", "perceptive hearing loss", "X-linked deafness type 2", "deafness, X-linked type 2", "sensorineural hearing loss", "high frequency hearing loss", "high-frequency hearing loss", "X-linked stapes gusher syndrome", "X-linked sensorineural deafness", "perceptive hearing loss or deafness", "perilymphatic gusher-deafness syndrome", "Perilymphatic gusher-deafness syndrome", "PERILYMPHATIC GUSHER-DEAFNESS SYNDROME", "conductive deafness with stapes fixation", "deafness mixed with perilymphatic gusher", "deafness, X-linked 2, X-linked recessive", "Progressive hearing loss stapes fixation", "mixed deafness with perilymphatic gusher", "deafness conductive with stapes fixation", "Deafness, mixed, with perilymphatic gusher", "Deafness, Conductive, with Stapes Fixation", "conductive deafness 3 with stapes fixation", "DEAFNESS, CONDUCTIVE, WITH STAPES FIXATION", "deafness, mixed, with perilymphatic gusher", "deafness 3 conductive with stapes fixation", "deafness, conductive, with stapes fixation", "DEAFNESS, MIXED, WITH PERILYMPHATIC GUSHER", "DFN 3 nonsyndromic hearing loss and deafness", "deafness 3, conductive, with stapes fixation", "Deafness 3, conductive, with stapes fixation", "DEAFNESS 3, CONDUCTIVE, WITH STAPES FIXATION", "X-linked mixed deafness with perilymphatic gusher", "deafness mixed with perilymphatic gusher, X-linked", "X-linked mixed conductive and neurosensory deafness", "X-linked mixed conductive and sensorineural deafness", "X-linked mixed hearing loss with perilymphatic gusher", "X-linked mixed conductive and neurosensory hearing loss", "X-linked mixed conductive and sensorineural hearing loss", "Sensorineural deafness, profound, with or without a conductive component", "Sensorineural Deafness, Profound, with or without a Conductive Component, Associated with a Unique Developmental Abnormality of the Ear", "SENSORINEURAL DEAFNESS, PROFOUND, WITH OR WITHOUT A CONDUCTIVE COMPONENT, ASSOCIATED WITH A UNIQUE DEVELOPMENTAL ABNORMALITY OF THE EAR", "sensorineural deafness, profound, with or without a conductive component, associated with a unique developmental Abnormality of the Ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked mixed hearing loss with perilymphatic gusher", "shortest_name_length": 4}
{"curie": "UMLS:C4526718", "names": ["Stage II", "Stage II Lung Cancer", "Stage II Lung Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Lung Cancer AJCC v8", "shortest_name_length": 8}
{"curie": "UMLS:C0221163", "names": ["MOTOR DISORDER", "Motor disorder", "motor disorder", "motor disorders", "disorder; motor", "disorders motor", "Motor Disorders", "motor; disorder", "Motor disease or syndrome", "Motor Diseases and Syndromes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Motor Disorders", "shortest_name_length": 14}
{"curie": "MONDO:0054835", "names": ["IPD", "DTDS", "PKDYS", "PKDYS1", "classic DTDS", "Infantile dystonia parkinsonism", "Infantile dystonia-parkinsonism", "Parkinsonism-dystonia infantile", "Parkinsonism-Dystonia, Infantile", "Parkinsonism-dystonia, infantile, 1", "PARKINSONISM-DYSTONIA, INFANTILE, 1", "dopamine transporter deficiency syndrome", "PARKINSONISM-DYSTONIA 1, INFANTILE-ONSET", "Dopamine Transporter Deficiency Syndrome", "Dopamine transporter deficiency syndrome", "DOPAMINE TRANSPORTER DEFICIENCY SYNDROME", "Infantile dystonia parkinsonism (disorder)", "classic dopamine transporter deficiency syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "classic dopamine transporter deficiency syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0007955", "names": ["ILEAL DIVERTICULA", "Diverticulum ilei", "Ileal diverticulum", "diverticulum meckel", "Meckel diverticulum", "Meckel Diverticulum", "MECKEL DIVERTICULUM", "meckel diverticulum", "Diverticulum, Meckel", "diverticulum; Meckel", "Meckel; diverticulum", "diverticulum meckels", "meckels diverticulum", "Meckels diverticulum", "Meckel's diverticulum", "Meckel's Diverticulum", "diverticulum meckel's", "meckel's diverticulum", "Diverticulum Meckel's", "Diverticulum of Meckel", "diverticulum meckels's", "duct; omphalomesenteric", "Persistent vitelline duct", "persistent vitelline duct", "MD - Meckel's diverticulum", "persistent; vitelline duct", "Meckel's diverticulum (disorder)", "persistent omphalomesenteric duct", "Meckel's diverticulum (diagnosis)", "Persistent omphalomesenteric duct", "persistent; omphalomesenteric duct", "Persistent intestinal end of vitelline duct", "persistent omphalomesenteric duct (diagnosis)", "Meckel's diverticulum (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meckel diverticulum", "shortest_name_length": 17}
{"curie": "MONDO:0005194", "names": ["Rotavirus disease", "rotavirus infection", "Rotavirus Infection", "Rotavirus infection", "rotavirus infections", "Rotavirus Infections", "Rotavirus infections", "Infection, Rotavirus", "Infections, Rotavirus", "Disease due to Rotavirus", "DISEASES DUE TO ROTAVIRUS", "Disease caused by Rotavirus", "Rotavirus infectious disease", "Disease due to Rotavirus, NOS", "Rotavirus disease or disorder", "Rotavirus caused disease or disorder", "Disease caused by Rotavirus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rotavirus infection", "shortest_name_length": 17}
{"curie": "MONDO:0014966", "names": ["PVNH7", "PERIVENTRICULAR NODULAR HETEROTOPIA 7", "periventricular nodular heterotopia 7", "periventricular nodular heterotopia type 7", "NEDD4L periventricular nodular heterotopia", "periventricular nodular heterotopia 7; PVNH7", "periventricular nodular heterotopia caused by mutation in NEDD4L"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "periventricular nodular heterotopia 7", "shortest_name_length": 5}
{"curie": "MONDO:0019108", "names": ["silent sinus syndrome", "Silent sinus syndrome", "Imploding antrum syndrome", "Silent sinus syndrome (disorder)", "Silent sinus syndrome (diagnosis)", "upper respiratory tract silent sinus syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "silent sinus syndrome", "shortest_name_length": 21}
{"curie": "UMLS:C1336468", "names": ["Stage I Nodular Lymphocyte Predominant Hodgkin Lymphoma", "Stage I Nodular Lymphocyte Predominant Hodgkin's Disease", "Stage I Nodular Lymphocyte Predominant Hodgkin's Lymphoma", "Stage I Hodgkin's Disease Nodular Lymphocyte Predominance Type", "Stage I Hodgkin's Lymphoma Nodular Lymphocyte Predominance Type", "Ann Arbor Stage I Nodular Lymphocyte Predominant Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage I Nodular Lymphocyte Predominant Hodgkin Lymphoma", "shortest_name_length": 55}
{"curie": "UMLS:C4055183", "names": ["Contrast-induced nephropathy", "contrast-induced nephropathy", "Contrast - Induced Nephropathy", "Contrast medium, radiography nephropathy", "contrast-induced nephropathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "contrast-induced nephropathy", "shortest_name_length": 28}
{"curie": "MONDO:0003428", "names": ["Brain Angioma", "brain angioma", "hemangioma brain", "brain hemangioma", "Brain Hemangioma", "BRAIN HEMANGIOMA", "brain hemangiomas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brain hemangioma", "shortest_name_length": 13}
{"curie": "UMLS:C3887901", "names": ["Refractory Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Carcinoma", "shortest_name_length": 20}
{"curie": "UMLS:C4521809", "names": ["Stage IIA Appendix Cancer", "Stage IIA Appendix Carcinoma AJCC v8", "Stage IIA Appendiceal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Appendix Carcinoma AJCC v8", "shortest_name_length": 25}
{"curie": "MONDO:0004158", "names": ["pancreatic invasive mucinous cystadenocarcinoma", "Pancreatic Invasive Mucinous Cystadenocarcinoma", "pancreatic mucinous cystic neoplasm with an associated invasive carcinoma", "pancreatic mucinous-cystic neoplasm with an associated invasive carcinoma", "Pancreatic Mucinous-Cystic Neoplasm with an Associated Invasive Carcinoma", "Pancreatic Mucinous Cystic Neoplasm with an Associated Invasive Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic mucinous-cystic neoplasm with an associated invasive carcinoma", "shortest_name_length": 47}
{"curie": "UMLS:C4687677", "names": ["Metastatic Neuroendocrine Tumor", "Metastatic Well Differentiated Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Neuroendocrine Tumor", "shortest_name_length": 31}
{"curie": "MONDO:0012910", "names": ["ARHI1", "presbycusis 1", "Presbycusis 1", "PRESBYCUSIS 1", "age-related hearing impairment 1", "Age-Related Hearing Impairment 1", "AGE-RELATED HEARING IMPAIRMENT 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "age-related hearing impairment 1", "shortest_name_length": 5}
{"curie": "MONDO:0001123", "names": ["sphenoidal sinus-chr.", "Sphenoidal sinus-chr.", "chronic sphenoid sinusitis", "sphenoid sinusitis, chronic", "chronic sphenoidal sinusitis", "Chronic Sphenoidal Sinusitis", "Chronic sphenoidal sinusitis", "Chronic sinusitis, sphenoidal", "Chronic sphenoidal sinusitis (disorder)", "chronic sphenoidal sinusitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic sphenoidal sinusitis", "shortest_name_length": 21}
{"curie": "UMLS:C1335715", "names": ["Pseudomelanoma", "Recurrent Nevus", "Persistent Nevus", "Traumatized Nevus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Nevus", "shortest_name_length": 14}
{"curie": "MONDO:0007216", "names": ["BDA2", "Brachymesophalangy 2", "Brachydactyly type A2", "brachymesophalangy II", "Type A2 brachydactyly", "brachydactyly type A2", "Brachymesophalangy Ii", "BRACHYMESOPHALANGY II", "BRACHYDACTYLY, TYPE A2", "Brachydactyly, Type A2", "brachydactyly, type A2", "Brachymesophalangy type 2", "Brachydactyly Mohr Wriedt type", "Mohr-Wriedt type brachydactyly", "MOHR-WRIEDT TYPE BRACHYDACTYLY", "brachydactyly, Mohr-Wriedt type", "Brachydactyly, Mohr-Wriedt type", "Brachydactyly type A2 (disorder)", "Short index fingers and second toes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly type A2", "shortest_name_length": 4}
{"curie": "MONDO:0017649", "names": ["HD-HA syndrome", "hemidystonia-hemiatrophy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemidystonia-hemiatrophy syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C0266963", "names": ["jaw abscess", "JAW ABSCESS", "Abscess jaw", "abscess; jaw", "jaw; abscess", "abscess of jaw", "Abscess of jaw", "Abscess of jaw, NOS", "Acute abscess of jaw", "Abscess of jaw, acute", "Abscess of jaw (disorder)", "abscess of jaw (diagnosis)", "Suppurative abscess of jaw", "Abscess of jaw, suppurative"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abscess of jaw", "shortest_name_length": 11}
{"curie": "UMLS:C4683596", "names": ["Lugano Classification Stage I Childhood Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage I Childhood Hodgkin Lymphoma AJCC v8", "shortest_name_length": 64}
{"curie": "MONDO:0032698", "names": ["NEDCPMD", "neurodevelopmental disorder with central and peripheral motor dysfunction", "NEURODEVELOPMENTAL DISORDER WITH CENTRAL AND PERIPHERAL MOTOR DYSFUNCTION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with central and peripheral motor dysfunction", "shortest_name_length": 7}
{"curie": "MONDO:0012410", "names": ["MPD3", "distal myopathy 3", "Myopathy, Distal 3", "MYOPATHY, DISTAL, 3", "myopathy, distal, 3", "Distal myopathy type 3", "distal myopathy type 3", "distal muscular dystrophy 3", "Finnish upper limb-onset distal myopathy", "Finnish upper limb onset distal myopathy", "Finnish upper limb onset distal myopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Finnish upper limb-onset distal myopathy", "shortest_name_length": 4}
{"curie": "UMLS:C4289319", "names": ["FIGO Stage IIIA1 Ovarian Cancer", "FIGO Stage IIIA1 Ovarian Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Stage IIIA1 Ovarian Cancer", "shortest_name_length": 31}
{"curie": "MONDO:0003834", "names": ["Gastric Cardia Cancer", "gastric cardia cancer", "gastric cardia carcinoma", "Gastric Cardia Carcinoma", "Cancer of Gastric Cardia", "cancer of gastric cardia", "Carcinoma of Gastric Cardia", "cardia of stomach carcinoma", "carcinoma of gastric cardia", "Cancer of the Gastric Cardia", "cancer of the gastric cardia", "carcinoma of Cardia of stomach", "Carcinoma of Cardia of Stomach", "carcinoma of cardia of stomach", "gastric cardia (stomach) cancer", "carcinoma of the gastric cardia", "Carcinoma of the Gastric Cardia", "Gastric Cardia (Stomach) Cancer", "carcinoma of the cardia of the stomach", "Carcinoma of the Cardia of the Stomach"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric cardia carcinoma", "shortest_name_length": 21}
{"curie": "UMLS:C4526733", "names": ["Lung Large Cell Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Large Cell Carcinoma by AJCC v7 Stage", "shortest_name_length": 42}
{"curie": "MONDO:0017336", "names": ["fatal infantile HCM due to mitochondrial complex I deficiency", "fatal infantile hypertrophic cardiomyopathy due to NADH-CoQ reductase deficiency", "fatal infantile hypertrophic cardiomyopathy due to mitochondrial complex I deficiency", "fatal infantile hypertrophic cardiomyopathy due to NADH-coenzyme Q reductase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fatal infantile hypertrophic cardiomyopathy due to mitochondrial complex I deficiency", "shortest_name_length": 61}
{"curie": "MONDO:0010673", "names": ["Tourette Syndrome, Modifier of", "TOURETTE SYNDROME, MODIFIER OF", "Tourette syndrome, modifier of", "Modifier, X-Linked, for Neurofunctional Defects", "MODIFIER, X-LINKED, FOR NEUROFUNCTIONAL DEFECTS", "modifier, X-linked, for Neurofunctional defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "modifier, X-linked, for Neurofunctional defects", "shortest_name_length": 30}
{"curie": "MONDO:0010263", "names": ["ATS-MR", "Ats-Mr", "AMME complex", "AMME Complex", "AMME COMPLEX", "AMME syndrome", "chromosome Xq22.3 telomeric deletion syndrome", "CHROMOSOME Xq22.3 TELOMERIC DELETION SYNDROME", "Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis", "Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis", "ALPORT SYNDROME, MENTAL RETARDATION, MIDFACE HYPOPLASIA, AND ELLIPTOCYTOSIS", "Alport syndrome, intellectual disability, midface hypoplasia, and elliptocytosis", "Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome", "Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome", "Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome (disorder)", "Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0002740", "names": ["Broad Ligament Mucinous Adenocarcinoma", "uterine ligament mucinous adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine ligament mucinous adenocarcinoma", "shortest_name_length": 38}
{"curie": "MONDO:0009862", "names": ["HPABH4C", "PKU type 2", "atypical pku", "Atypical PKU", "PKU, Atypical", "dhpr deficiency", "QDPR DEFICIENCY", "Qdpr deficiency", "DHPR deficiency", "QDPR Deficiency", "DHPR DEFICIENCY", "DHPR Deficiency", "Deficiency, DHPR", "Deficiency, QDPR", "Phenylketonuria II", "Phenylketonuria type 2", "phenylketonuria type 2", "Phenylketonuria Type 2", "Atypical phenylketonuria", "Atypical Phenylketonuria", "Phenylketonuria, atypical", "Phenylketonuria, Atypical", "Hyperphenylalaninemia, type IV", "Hyperphenylalaninaemia, type IV", "Dihydropteridine Reductase Deficiency", "Dihydropteridine reductase deficiency", "dihydropteridine reductase deficiency", "BH4-deficient hyperphenylalaninemia C", "DIHYDROPTERIDINE REDUCTASE DEFICIENCY", "hyperphenylalaninemia, BH4-deficient C", "Hyperphenylalaninemia, BH4-deficient C", "Deficiency, Dihydropteridine Reductase", "Hyperphenylalaninemia, BH4-Deficient, C", "HYPERPHENYLALANINEMIA, BH4-DEFICIENT, C", "hyperphenylalaninemia, BH4-deficient, C", "hyperphenylalaninemia, BH-4-deficient, C", "DHPR - Dihydropteridine reductase deficiency", "hyperphenylalaninemia, Bh4-deficient, type C", "Dihydropteridine Reductase Deficiency Disease", "quinoid dihydropteridine reductase deficiency", "QUINOID DIHYDROPTERIDINE REDUCTASE DEFICIENCY", "Quinoid Dihydropteridine Reductase Deficiency", "Deficiency Disease, Dihydropteridine Reductase", "6,7-dihydropteridine reductase activity disease", "Dihydropteridine reductase deficiency (disorder)", "disorder of 6,7-dihydropteridine reductase activity", "hyperphenylalaninemia due to dihydropteridine reductase deficiency", "Hyperphenylalaninemia due to dihydropteridine reductase deficiency", "hyperphenylalaninemia, tetrahydrobiopterin-deficient, due to DHPR deficiency", "HYPERPHENYLALANINEMIA, TETRAHYDROBIOPTERIN-DEFICIENT, DUE TO DHPR DEFICIENCY", "Hyperphenylalaninemia, Tetrahydrobiopterin-Deficient, Due To DHPR Deficiency", "tetrahydrobiopterin (BH4)-deficient hyperphenylalaninemia due to dihydropteridine reductase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dihydropteridine reductase deficiency", "shortest_name_length": 7}
{"curie": "MONDO:0017399", "names": ["RTLA", "rvFTD", "Right temporal lobar atrophy", "Right temporal atrophy variant frontotemporal dementia", "frontotemporal dementia right temporal atrophy variant", "frontotemporal dementia, right temporal atrophy variant", "Right temporal atrophy variant frontotemporal dementia (disorder)", "Right temporal atrophy variant frontotemporal dementia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontotemporal dementia, right temporal atrophy variant", "shortest_name_length": 4}
{"curie": "MONDO:0016011", "names": ["FAS", "FAE", "ARND", "FASD", "ARBD", "fetal alcohol effect", "fetal alcohol effects", "alcoholic embryopathy", "static encephalopathy", "Fetal Alcohol Syndrome", "alcohol fetal syndrome", "fetal alcohol syndrome", "Fetal alcohol syndrome", "FETAL ALCOHOL SYNDROME", "Syndrome, Fetal Alcohol", "foetal alcohol syndrome", "FOETAL ALCOHOL SYNDROME", "fetus; alcohol syndrome", "Foetal alcohol syndrome", "embryopathia alcoholica", "alcohol; syndrome, fetal", "FAS - Fetal alcohol syndrome", "fetal alcohol syndrome (FAS)", "embryofetal alcohol syndrome", "Alcohol-related birth defects", "FAS - Foetal alcohol syndrome", "alcohol-related birth defects", "fetal alcohol spectrum disorders", "Fetal Alcohol Spectrum Disorders", "Fetal alcohol spectrum disorders", "Fetal alcohol syndrome (disorder)", "fetal alcohol syndrome (diagnosis)", "embryofetal alcohol syndrome (EFAS)", "Fetal alcohol syndrome (dysmorphic)", "alcohol; fetal syndrome (dysmorphic)", "fetal; alcohol syndrome (dysmorphic)", "alcohol; syndrome, fetal (dysmorphic)", "syndrome; fetal, alcohol (dysmorphic)", "syndrome; alcohol, fetal (dysmorphic)", "alcohol-related neurodevelopmental disorder", "Alcohol-related neurodevelopmental disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fetal alcohol syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0001973", "names": ["Brucella abortus brucellosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brucella abortus brucellosis", "shortest_name_length": 28}
{"curie": "UMLS:C1384687", "names": ["Ancylostoma duodenale infection", "infection by Ancylostoma duodenale", "Ancylostomiasis due to ancylostoma duodenale", "Ancylostomiasis due to Ancylostoma Duodenale", "Ancylostomiasis due to Ancylostoma duodenale", "infection by Ancylostoma duodenale (diagnosis)", "Ancylostomiasis caused by Ancylostoma duodenale", "Ancylostomiasis caused by Ancylostoma duodenale (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ancylostomiasis due to Ancylostoma duodenale", "shortest_name_length": 31}
{"curie": "UMLS:C1336249", "names": ["stage III hypopharynx cancer", "hypopharynx cancer, stage III", "Stage III Hypopharynx Carcinoma", "stage III hypopharyngeal cancer", "hypopharyngeal cancer, stage III", "Stage III Carcinoma of Hypopharynx", "Stage III Hypopharyngeal Carcinoma", "Stage III Hypopharyngeal Throat Cancer", "Stage III Carcinoma of the Hypopharynx", "Stage III Hypopharynx Carcinoma AJCC v6", "Stage III Hypopharyngeal Carcinoma AJCC v6", "Stage III Carcinoma of Hypopharynx AJCC v6", "Stage III Carcinoma of the Hypopharynx AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Hypopharyngeal Carcinoma AJCC v6", "shortest_name_length": 28}
{"curie": "UMLS:C0338422", "names": ["HIV leukoencephalopathy", "HIV Leukoencephalopathy", "HIV leukoencephalopathy (diagnosis)", "Human immunodefiency virus leucoencephalopathy", "Human immunodeficiency virus leukoencephalopathy", "Human immunodeficiency virus leucoencephalopathy", "HIV - Human immunodefiency virus leucoencephalopathy", "HIV - Human immunodeficiency virus leucoencephalopathy", "HIV - Human immunodeficiency virus leukoencephalopathy", "Human immunodeficiency virus leukoencephalopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Human immunodeficiency virus leukoencephalopathy", "shortest_name_length": 23}
{"curie": "UMLS:C0862981", "names": ["Resectable Cholangiocarcinoma", "Cholangiocarcinoma resectable", "Resectable Cholangiocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cholangiocarcinoma resectable", "shortest_name_length": 29}
{"curie": "MONDO:0011343", "names": ["FOLLICULAR ATROPHODERMA, PERIORAL PIGMENTED, WITH MILIA AND EPIDERMOID CYSTS", "Follicular Atrophoderma, Perioral Pigmented, with Milia and Epidermoid Cysts", "follicular atrophoderma, perioral pigmented, with milia and epidermoid cysts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "follicular atrophoderma, perioral pigmented, with milia and epidermoid cysts", "shortest_name_length": 76}
{"curie": "UMLS:C5243996", "names": ["Cardiac Cirrhosis", "Congestive Hepatopathy", "Congestive hepatopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congestive hepatopathy", "shortest_name_length": 17}
{"curie": "UMLS:C3273130", "names": ["Extrahepatic Bile Duct BilIN", "Extrahepatic Bile Duct Dysplasia", "Extrahepatic Bile Duct Biliary Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extrahepatic Bile Duct Biliary Intraepithelial Neoplasia", "shortest_name_length": 28}
{"curie": "MONDO:0008133", "names": ["OPA3", "ADOAC", "optic atrophy 3", "OPA3, autosomal dominant", "Opa3, Autosomal Dominant", "optic atrophy 3 with cataract", "autosomal dominant optic atrophy 3", "optic atrophy 3, autosomal dominant", "OPTIC ATROPHY 3, AUTOSOMAL DOMINANT", "Optic Atrophy 3, Autosomal Dominant", "autosomal dominant optic atrophy type 3", "Autosomal dominant optic atrophy type 3", "autosomal dominant optic atrophy and cataract", "Autosomal dominant optic atrophy and cataract", "optic atrophy and cataract, autosomal dominant", "OPTIC ATROPHY AND CATARACT, AUTOSOMAL DOMINANT", "Optic atrophy and cataract, autosomal dominant", "optic atrophy, cataract, and neurologic disorder", "Optic atrophy, cataract, and neurologic disorder", "Autosomal dominant optic atrophy and cataract (disorder)", "Autosomal dominant optic atrophy and cataract (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "optic atrophy 3", "shortest_name_length": 4}
{"curie": "MONDO:0013724", "names": ["BACTS2", "bacteremia, susceptibility to", "CISH bacteremia, susceptibility", "bacteremia, susceptibility to, 2", "BACTEREMIA, SUSCEPTIBILITY TO, 2", "bacteremia, susceptibility to, type 2", "bacteremia, susceptibility caused by mutation in CISH"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bacteremia, susceptibility to, 2", "shortest_name_length": 6}
{"curie": "UMLS:C5206338", "names": ["Locally Advanced Unresectable Esophageal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Unresectable Esophageal Adenocarcinoma", "shortest_name_length": 55}
{"curie": "MONDO:0007132", "names": ["anonychia-ectrodactyly", "Anonychia-Ectrodactyly", "ANONYCHIA-ECTRODACTYLY", "anonychia ectrodactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anonychia-ectrodactyly", "shortest_name_length": 22}
{"curie": "MONDO:0100471", "names": ["AVITAMINOSIS D", "avitaminosis D", "Avitaminosis D", "VITAMIN D DEFIC", "DEFIC VITAMIN D", "Hypovitaminosis D", "avitaminosis D, NOS", "Avitaminosis D, NOS", "Vitamin D Deficiency", "d deficiency vitamin", "d vitamin deficiency", "VITAMIN D DEFICIENCY", "deficiency vitamin d", "VITAMIN DEFICIENCY D", "vitamin d deficiency", "vitamin D deficiency", "Vitamin D deficiency", "d deficiency vitamins", "deficiency, vitamin D", "Deficiency, Vitamin D", "deficiency; vitamin, D", "vitamin D deficiencies", "Vitamin D Deficiencies", "d deficiencies vitamin", "Deficient in vitamin D", "vitamin d deficiencies", "vitamin; deficiency, D", "d deficiencies vitamins", "Low levels of vitamin D", "Deficiencies, Vitamin D", "deficiencies, vitamin D", "vitamin D insufficiency", "Vitamin D deficiency, NOS", "vitamin D deficiency, NOS", "avitaminosis D (diagnosis)", "vitamin D deficiency (disorder)", "Vitamin D deficiency (disorder)", "vitamin D deficiency (diagnosis)", "Unspecified vitamin D deficiency", "Vitamin D deficiency, unspecified", "deficiency of vitamin D (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitamin D deficiency", "shortest_name_length": 14}
{"curie": "UMLS:C4744553", "names": ["Metastatic Hypopharyngeal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Hypopharyngeal Carcinoma", "shortest_name_length": 35}
{"curie": "MONDO:0020164", "names": ["epicanthal fold"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epicanthal fold", "shortest_name_length": 15}
{"curie": "UMLS:C0750970", "names": ["Cytotoxic Brain Edema", "Brain Edema, Cytotoxic", "Edema, Cytotoxic Brain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cytotoxic Brain Edema", "shortest_name_length": 21}
{"curie": "MONDO:0007689", "names": ["GUK3", "GUANYLATE KINASE 3", "guanylate kinase 3", "guanylate KINASE 3", "guanylate kinase type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "guanylate kinase 3", "shortest_name_length": 4}
{"curie": "MONDO:0014407", "names": ["MPPH2", "MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 2", "megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2", "megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome type 2", "AKT3 megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome", "megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome caused by mutation in AKT3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2", "shortest_name_length": 5}
{"curie": "UMLS:C3472615", "names": ["KSHV-8+ Extracavity Lymphoma", "KSHV-8 Positive Extracavity Lymphoma", "KSHV-Associated Non-Hodgkin Lymphoma", "Kaposi's Sarcoma-Associated Human Herpes Virus 8+ Extracavity Lymphoma", "Kaposi Sarcoma-Associated Human Herpes Virus 8 Positive Extracavity Lymphoma", "Kaposi's Sarcoma-Associated Human Herpes Virus 8 Positive Extracavity Lymphoma", "Large B-cell lymphoma arising in HHV8 associated multicentric Castleman disease", "Large B-Cell Lymphoma Arising in HHV8-Associated Multicentric Castleman Disease", "Large B-cell lymphoma arising in HHV8-associated multicentric Castleman disease", "Large B-Cell Lymphoma Arising in HHV 8-Associated Multicentric Castleman Disease", "Diffuse Large B-Cell Lymphoma Arising in HHV8-Positive Multicentric Castleman Disease", "Large B-cell lymphoma arising in HHV8-associated multicentric Castleman disease (disorder)", "Large B-cell lymphoma arising in HHV8-associated multicentric Castleman disease (diagnosis)", "Large B-Cell Lymphoma Arising in Human Herpes Virus 8-Associated Multicentric Castleman Disease", "Large B-cell lymphoma arising in human herpesvirus type 8 associated multicentric Castleman disease", "Large B-cell lymphoma arising in human herpesvirus type 8 associated multicentric Castleman disease (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Large B-cell lymphoma arising in HHV8 associated multicentric Castleman disease", "shortest_name_length": 28}
{"curie": "UMLS:C0581883", "names": ["Deafness total", "Total Deafness", "Complete deafness", "Complete Deafness", "Total Hearing Loss", "Deafness, complete", "complete hearing loss", "Complete hearing loss", "Complete Hearing Loss", "Hearing Loss, Complete", "Complete deafness (disorder)", "total hearing loss bilaterally", "total hearing loss bilaterally (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Complete Hearing Loss", "shortest_name_length": 14}
{"curie": "MONDO:0100362", "names": ["lip herpes simplex type 2 infectious disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lip herpes simplex type 2 infectious disorder", "shortest_name_length": 45}
{"curie": "UMLS:C3544205", "names": ["Ovarian clear cell carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian clear cell carcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0002857", "names": ["Gallbladder Sarcoma", "gallbladder sarcoma", "gall bladder sarcoma", "sarcoma of gallbladder", "Sarcoma of Gallbladder", "sarcoma of gall bladder", "sarcoma of the gallbladder", "Sarcoma of the Gallbladder", "sarcoma of gallbladder (diagnosis)", "malignant mesenchymal tumor of gallbladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gallbladder sarcoma", "shortest_name_length": 19}
{"curie": "MONDO:0017228", "names": ["AIP type 2", "duct-centric pancreatitis", "autoimmune pancreatitis type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune pancreatitis type 2", "shortest_name_length": 10}
{"curie": "UMLS:C4727418", "names": ["Recurrent Submandibular Gland Undifferentiated Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Submandibular Gland Undifferentiated Carcinoma", "shortest_name_length": 56}
{"curie": "MONDO:0060765", "names": ["Fibroepithelial Polyp", "fibroepithelial polyp", "FIBROPAPILLOMA, BENIGN", "fibropapilloma, benign"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibroepithelial polyp", "shortest_name_length": 21}
{"curie": "MONDO:0060664", "names": ["NEDMCR", "NEDMCR syndrome", "neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities", "NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CATARACTS, AND RENAL ABNORMALITIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities", "shortest_name_length": 6}
{"curie": "MONDO:0015689", "names": ["myeloid/lymphoid neoplasms with PDGFRA rearrangement", "Myeloid/Lymphoid Neoplasms with PDGFRA Rearrangement", "myeloid neoplasm associated with PDGFRA rearrangement", "Myeloid or lymphoid neoplasm with PDGFRA rearrangement", "Myeloid and lymphoid neoplasms with PDGFRA rearrangement", "myeloid and lymphoid neoplasms with PDGFRA rearrangement", "Myeloid and Lymphoid Neoplasms with PDGFRA Rearrangement", "Myeloid/lymphoid neoplasm associated with PDGFRA rearrangement", "myeloid/lymphoid neoplasm associated with PDGFRA rearrangement", "myeloid and lymphoid neoplasms associated with PDGFRA rearrangement", "Myeloid or lymphoid neoplasm with alpha-type platelet-derived growth factor receptor gene rearrangement", "Myeloid and/or lymphoid neoplasm associated with platelet derived growth factor receptor alpha rearrangement", "Myeloid and/or lymphoid neoplasm associated with platelet derived growth factor receptor alpha rearrangement (disorder)", "Myeloid or lymphoid neoplasm with alpha-type platelet-derived growth factor receptor gene rearrangement (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myeloid neoplasm associated with PDGFRA rearrangement", "shortest_name_length": 52}
{"curie": "UMLS:C2981378", "names": ["Stage IIA Small Intestinal Cancer", "Stage IIA Small Intestinal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Small Intestinal Cancer AJCC v7", "shortest_name_length": 33}
{"curie": "UMLS:C4331328", "names": ["Stage III Major Salivary Gland Cancer", "Stage III Major Salivary Gland Cancer AJCC v8", "Stage III Major Salivary Gland Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Major Salivary Gland Cancer AJCC v8", "shortest_name_length": 37}
{"curie": "UMLS:C4285735", "names": ["Acute myopia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute myopia", "shortest_name_length": 12}
{"curie": "MONDO:0012097", "names": ["SCDO2", "spondylocostal dysostosis 2", "Autosomal recessive spondylocostal dysostosis", "Spondylocostal dysostosis, autosomal recessive", "autosomal recessive spondylocostal dysostosis 2", "spondylocostal dysostosis 2, autosomal recessive", "SPONDYLOCOSTAL DYSOSTOSIS 2, AUTOSOMAL RECESSIVE", "Spondylocostal Dysostosis 2, Autosomal Recessive", "SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondylocostal dysostosis 2, autosomal recessive", "shortest_name_length": 5}
{"curie": "UMLS:C0852952", "names": ["optic nerve cup", "Optic nerve cupping", "optic nerve cupping", "cupping of optic nerve", "Cupping of optic nerve"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Optic nerve cupping", "shortest_name_length": 15}
{"curie": "UMLS:C0154023", "names": ["Benign Orbit Tumor", "Benign orbital tumor", "Benign Orbital Tumor", "Benign tumor of orbit", "Benign Orbit Neoplasm", "Benign orbital tumour", "Benign Tumor of Orbit", "Benign tumour of orbit", "benign orbital neoplasm", "Benign Orbital Neoplasm", "Benign Neoplasm of Orbit", "Benign neoplasm of orbit", "benign neoplasm of orbit", "Benign Tumor of the Orbit", "Benign Neoplasm of the Orbit", "Benign neoplasm of orbit (disorder)", "benign neoplasm of orbit (diagnosis)", "Benign neoplasm of orbit, unspecified", "Benign neoplasm of unspecified site of orbit"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign neoplasm of orbit", "shortest_name_length": 18}
{"curie": "MONDO:0000421", "names": ["serine deficiency", "inborn serine deficiency", "inborn L-serine biosynthetic process disorder", "inborn error of L-serine biosynthetic process", "rare inborn error of L-serine biosynthetic process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn serine deficiency", "shortest_name_length": 17}
{"curie": "UMLS:C4553786", "names": ["stage 0is ureter cancer", "Stage 0is Ureter Cancer", "Stage 0is Ureter Cancer AJCC v8", "stage 0is ureter cancer AJCC v8", "Stage 0is Ureter Urothelial Carcinoma AJCC v8", "stage 0is ureter urothelial carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0is Ureter Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "MONDO:0003255", "names": ["mediastinum granular cell tumor", "Mediastinal Granular Cell Tumor", "mediastinal granular cell tumor", "Mediastinal Granular Cell Neoplasm", "Granular Cell Tumor of Mediastinum", "granular cell tumor of mediastinum", "mediastinal granular cell neoplasm", "granular cell neoplasm of mediastinum", "Granular Cell Neoplasm of Mediastinum", "mediastinal granular cell myoblastoma", "Mediastinal Granular Cell Myoblastoma", "granular cell tumor of the mediastinum", "Granular Cell Tumor of the Mediastinum", "granular cell myoblastoma of mediastinum", "Granular Cell Myoblastoma of Mediastinum", "Granular Cell Neoplasm of the Mediastinum", "granular cell neoplasm of the mediastinum", "Granular Cell Myoblastoma of the Mediastinum", "granular cell myoblastoma of the mediastinum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mediastinal granular cell myoblastoma", "shortest_name_length": 31}
{"curie": "UMLS:C1096452", "names": ["Neonatal Early-Onset Sepsis", "Early-Onset Neonatal Sepsis", "Neonatal Early-Onset Sepses", "Neonatal Early Onset Sepsis", "Early onset neonatal sepsis", "Early-onset neonatal sepsis", "Early-Onset Sepses, Neonatal", "Early-Onset Sepsis, Neonatal", "Sepsis, Neonatal Early-Onset", "Neonatal Sepsis, Early-Onset", "Sepses, Neonatal Early-Onset", "septicemia of newborn early-onset", "Early-onset neonatal sepsis (disorder)", "Early-onset neonatal sepsis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neonatal Early-Onset Sepsis", "shortest_name_length": 27}
{"curie": "MONDO:0011099", "names": ["BSAS", "ABDS", "ABSD", "human HOXA1 syndromes", "Human HOXA1 syndromes", "NAVAJO BRAINSTEM SYNDROME", "Navajo brainstem syndrome", "Bosley-Salih-Alorainy syndrome", "Bosley Salih Alorainy syndrome", "BOSLEY-SALIH-ALORAINY SYNDROME", "Bosley-Salih-Alorainy Syndrome", "Athabaskan brainstem dysgenesis", "Athabaskan Brainstem Dysgenesis Syndrome", "ATHABASKAN BRAINSTEM DYSGENESIS SYNDROME", "Athabascan brainstem dysgenesis syndrome", "Athabaskan brainstem dysgenesis syndrome", "Bosley Salih Alorainy syndrome (disorder)", "Athabaskan brainstem dysgenesis syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "human HOXA1 syndromes", "shortest_name_length": 4}
{"curie": "UMLS:C1334922", "names": ["Nasal Cavity Non-Hodgkin Lymphoma", "Nasal Cavity Non-Hodgkin's Lymphoma", "Non-Hodgkin's Lymphoma of Nasal Cavity", "non-Hodgkin's lymphoma of nasal cavity", "Non-Hodgkin's Lymphoma of the Nasal Cavity", "non-Hodgkin's lymphoma of nasal cavity (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-Hodgkin's lymphoma of nasal cavity", "shortest_name_length": 33}
{"curie": "MONDO:0015431", "names": ["r10", "Ring 10", "r(10) syndrome", "Ring chromosome 10", "chromosome 10 ring", "Chromosome 10 ring", "ring chromosome 10", "Ring chromosome type 10", "chromosome 10 ring syndrome", "ring chromosome 10 syndrome", "Ring chromosome 10 syndrome", "Ring chromosome 10 syndrome (disorder)", "Ring chromosome 10 syndrome (diagnosis)", "anomaly of chromosome pair ring 10 syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ring chromosome 10", "shortest_name_length": 3}
{"curie": "UMLS:C1536503", "names": ["Cryogenic Burn", "Cryogenic burn"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cryogenic Burn", "shortest_name_length": 14}
{"curie": "UMLS:C0205699", "names": ["carcinosis", "CARCINOMATOSIS", "carcinomatosis", "Carcinomatosis", "Carcinomatoses", "[M]Carcinomatosis", "Carcinomatosis NOS", "Carcinomatosis (disorder)", "Disseminated carcinomatosis", "Carcinomatosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carcinomatosis", "shortest_name_length": 10}
{"curie": "MONDO:0005266", "names": ["diabetic retinopathy", "Diabetic Retinopathy", "Retinopathy;diabetic", "Retinopathy diabetic", "DIABETIC RETINOPATHY", "Diabetic retinopathy", "Retinopathy, Diabetic", "Retinopathy, diabetic", "Diabetic Retinopathies", "Retinopathies, Diabetic", "Diabetic retinopathy NOS", "Diabetic retinopathy, NOS", "DR - Diabetic retinopathy", "diabetes with diabetic retinopathy", "Retinopathy due to diabetes mellitus", "retinal abnormality - diabetes-related", "Retinal abnormality - diabetes-related", "diabetes mellitus with diabetic retinopathy", "diabetes with diabetic retinopathy (diagnosis)", "Retinopathy due to diabetes mellitus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diabetic retinopathy", "shortest_name_length": 20}
{"curie": "MONDO:0040500", "names": ["MRT62", "GPIBD16", "mental retardation, autosomal recessive 62", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 62", "intellectual disability, autosomal recessive 62", "GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 16", "glycosylphosphatidylinositol biosynthesis defect 16", "Intellectual developmental disorder, autosomal recessive 62"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycosylphosphatidylinositol biosynthesis defect 16", "shortest_name_length": 5}
{"curie": "UMLS:C0751364", "names": ["Embryonal Cancer", "Cancer, Embryonal", "Embryonal Cancers", "Cancers, Embryonal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cancer, Embryonal", "shortest_name_length": 16}
{"curie": "UMLS:C1297929", "names": ["Breast Atypical Hyperplasia", "Atypical breast hyperplasia", "atypical breast hyperplasia", "atypical hyperplasia breast", "Atypical Breast Hyperplasia", "breast atypical hyperplasia", "Atypical hyperplasia of breast", "atypical hyperplasia of breast", "Atypical Hyperplasia of Breast", "Atypical Hyperplasia of the Breast", "Atypical hyperplasia of breast (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypical hyperplasia of breast", "shortest_name_length": 27}
{"curie": "MONDO:0011307", "names": ["SCZD2", "SCHIZOPHRENIA 2", "schizophrenia 2", "schizophrenia susceptibility locus, chromosome 11Q-related", "SCHIZOPHRENIA SUSCEPTIBILITY LOCUS, CHROMOSOME 11q-RELATED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schizophrenia 2", "shortest_name_length": 5}
{"curie": "MONDO:0016443", "names": ["Nevus anelasticus", "Naevus anelasticus", "eruptive collagenoma", "Eruptive Collagenoma", "Eruptive collagenoma", "papular elastorrhexis", "Nevus anelasticus (disorder)", "disseminated nevus anelasticus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papular elastorrhexis", "shortest_name_length": 17}
{"curie": "MONDO:0010718", "names": ["Radial aplasia, X-linked", "RADIAL APLASIA, X-LINKED", "radial aplasia, X-linked", "radius absent anogenital anomalies", "Radius absent anogenital anomalies", "radial aplasia and anogenital anomalies", "RADIAL APLASIA AND ANOGENITAL ANOMALIES", "Radial Aplasia And Anogenital Anomalies", "absent radius-anogenital anomalies syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "absent radius-anogenital anomalies syndrome", "shortest_name_length": 24}
{"curie": "MONDO:0035004", "names": ["serine biosynthesis pathway deficiency, infantile/juvenile form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "serine biosynthesis pathway deficiency, infantile/juvenile form", "shortest_name_length": 63}
{"curie": "MONDO:0005960", "names": ["Silicosis", "Silicoses", "SILICOSIS", "silicosis", "silicatosis", "Silicatosis", "Silicosis NOS", "Silicosis, NOS", "acute silicosis", "Nodular silicosis", "chronic silicosis", "nodular silicosis", "silicotuberculosis", "sandblaster's lung", "silicosis (diagnosis)", "Silica pneumoconiosis", "accelerated silicosis", "sandblaster's; asthma", "silica pneumoconiosis", "silica; pneumoconiosis", "experimental silicosis", "pneumoconiosis; silica", "fibrosis; lung, silicotic", "lung; fibrosis, silicotic", "silicotic fibrosis of lung", "Silicotic fibrosis of lung", "Pneumoconiosis due to silica", "pneumoconiosis due to silica", "sandblaster's; pneumoconiosis", "Pneumoconiosis caused by silica", "pneumoconiosis due to silicates", "pneumoconiosis caused by silica", "Pneumoconiosis due to silicates", "Pneumoconiosis due to silica, NOS", "Pneumoconiosis caused by silica (disorder)", "Pneumoconiosis due to dust containing silica", "Pneumoconiosis due to other silica or silicates"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "silicosis", "shortest_name_length": 9}
{"curie": "UMLS:C1142499", "names": ["GI Toxicity", "Gastrointestinal toxicity", "gastrointestinal toxicity", "Gastrointestinal Toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal toxicity", "shortest_name_length": 11}
{"curie": "UMLS:C2728316", "names": ["SCI", "Silent Stroke", "silent stroke", "silent stroke (diagnosis)", "Silent Cerebral Infarction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "silent stroke", "shortest_name_length": 3}
{"curie": "UMLS:C4525349", "names": ["I", "Stage I Intrahepatic Cholangiocarcinoma AJCC v8", "Stage I Intrahepatic Bile Duct Cancer (Cholangiocarcinoma)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Intrahepatic Cholangiocarcinoma AJCC v8", "shortest_name_length": 1}
{"curie": "UMLS:C0334362", "names": ["borderline papillary serous cystadenoma", "Borderline Papillary Serous Cystadenoma", "Atypical proliferative papillary serous tumor", "Low Malignant Potential Papillary Serous Tumor", "Atypical proliferative papillary serous tumour", "low malignant potential papillary serous tumor", "low malignant potential papillary serous neoplasm", "Papillary Serous Tumor of Low Malignant Potential", "Low Malignant Potential Papillary Serous Neoplasm", "papillary serous tumor of low malignant potential", "Papillary serous tumor of low malignant potential", "Borderline Malignancy Papillary Serous Cystadenoma", "Papillary serous tumour of low malignant potential", "borderline malignancy papillary serous cystadenoma", "Papillary serous cystadenoma, borderline malignancy", "Papillary Serous Neoplasm of Low Malignant Potential", "Papillary serous cystadenoma - borderline malignancy", "papillary serous neoplasm of low malignant potential", "Low Malignancy Potential Papillary Serous Cystadenoma", "low malignancy potential papillary serous cystadenoma", "Serous papillary cystic tumor of borderline malignancy", "Serous papillary cystic tumour of borderline malignancy", "[M] Papillary serous cystadenoma, borderline malignancy", "Serous papillary cystic tumor of borderline malignancy (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Serous papillary cystic tumor of borderline malignancy", "shortest_name_length": 39}
{"curie": "MONDO:0007840", "names": ["internal carotid artery, spontaneous dissection of", "Internal Carotid Artery, Spontaneous Dissection of", "INTERNAL CAROTID ARTERY, SPONTANEOUS DISSECTION OF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "internal carotid artery, spontaneous dissection of", "shortest_name_length": 50}
{"curie": "MONDO:0020697", "names": ["Lung Epithelial-Myoepithelial Cancer", "lung epithelial-myoepithelial cancer", "lung epithelial-myoepithelial carcinoma", "Lung Epithelial-Myoepithelial Carcinoma", "epithelial-myoepithelial carcinoma of lung", "epithelial-myoepithelial carcinoma of lung (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung epithelial-myoepithelial carcinoma", "shortest_name_length": 36}
{"curie": "MONDO:0004403", "names": ["childhood T lymphoblastic leukemia/lymphoma", "Childhood T Lymphoblastic Leukemia/Lymphoma", "Childhood T-Lymphoblastic Leukemia/Lymphoma", "Childhood T-Cell Lymphoblastic Leukemia/Lymphoma", "pediatric precursor T-lymphoblastic lymphoma/leukemia", "Childhood Precursor T-Lymphoblastic Lymphoma/Leukemia", "childhood precursor T-lymphoblastic lymphoma/leukemia", "precursor T-lymphoblastic lymphoma/leukemia of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood precursor T-lymphoblastic lymphoma/leukemia", "shortest_name_length": 43}
{"curie": "MONDO:0020346", "names": ["synaptic congenital myasthenic syndrome", "synaptic congenital myasthenic syndromes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "synaptic congenital myasthenic syndrome", "shortest_name_length": 39}
{"curie": "UMLS:C1541317", "names": ["Gliosarcoma", "Adult Gliosarcoma", "adult gliosarcoma", "gliosarcoma, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Gliosarcoma", "shortest_name_length": 11}
{"curie": "UMLS:C4764085", "names": ["Refractory Richter Syndrome", "Refractory Transformed Chronic Lymphocytic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Transformed Chronic Lymphocytic Leukemia", "shortest_name_length": 27}
{"curie": "UMLS:C0751021", "names": ["Crescendo Transient Ischemic Attacks", "Transient Ischemic Attacks, Crescendo"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Crescendo Transient Ischemic Attacks", "shortest_name_length": 36}
{"curie": "MONDO:0010816", "names": ["Qazi Markouizos syndrome", "Qazi-Markouizos syndrome", "Puertorican infant hypotonia syndrome", "PUERTO RICAN infant hypotonia syndrome", "Puerto Rican Infant Hypotonia Syndrome", "Puerto Rican infant hypotonia syndrome", "PUERTO RICAN INFANT HYPOTONIA SYNDROME", "Puerto Rican infant hypotonia syndrome (disorder)", "Dysharmonic skeletal maturation muscular fibre disproportion", "Dysharmonic skeletal maturation - muscular fibre disproportion", "Dysharmonic skeletal maturation-muscular fiber disproportion syndrome", "Dysharmonic skeletal maturation and muscular fibre disproportion syndrome", "Dysharmonic skeletal maturation and muscular fiber disproportion syndrome", "hypotonia, psychomotor retardation, seizures, delayed and Dysharmonic skeletal maturation, and congenital fibre type disproportion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Qazi Markouizos syndrome", "shortest_name_length": 24}
{"curie": "UMLS:C1708649", "names": ["Laryngeal Adenosquamous Carcinoma", "Laryngeal Throat Adenosquamous Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laryngeal Adenosquamous Carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0006191", "names": ["Clear cell carcinoma", "Clear cell endometrial carcinoma", "endometrial clear cell carcinoma", "clearcell carcinoma of the uterus", "carcinoma, clearcell, endometrial", "uterus cancer, clearcell carcinoma", "carcinoma of the uterus, clearcell", "Clear cell carcinoma of Endometrium", "Clear Cell Carcinoma of Endometrium", "uterine cancer, clearcell carcinoma", "clear cell carcinoma of endometrium", "endometrium clear cell adenocarcinoma", "endometrial clear cell adenocarcinoma", "Endometrial Clear Cell Adenocarcinoma", "Clear Cell Carcinoma of the Endometrium", "clear cell carcinoma of the endometrium", "uterine corpus cancer, clearcell carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometrial clear cell adenocarcinoma", "shortest_name_length": 20}
{"curie": "MONDO:0002752", "names": ["ovary adenocarcinoma", "adenocarcinoma ovary", "OVARY, ADENOCARCINOMA", "adenocarcinoma ovaries", "adenocarcinoma ovarian", "ovarian adenoacanthoma", "Ovarian adenocarcinoma", "ovarian adenocarcinoma", "Ovarian Adenocarcinoma", "Adenocarcinoma of ovary", "adenocarcinoma of ovary", "Adenocarcinoma of Ovary", "adenocarcinoma of the ovary", "Adenocarcinoma of the Ovary", "OVARIAN CANCER, ADENOCARCINOMA", "adenocarcinoma of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian adenocarcinoma", "shortest_name_length": 20}
{"curie": "MONDO:0036595", "names": ["Androblastoma", "androblastoma", "androblastomas", "arrhenoblastoma", "Arrhenoblastoma", "arrhenoblastomas", "Androblastoma NOS", "Androblastoma, NOS", "Arrhenoblastoma, NOS", "Androblastoma of ovary", "arrhenoblastoma of ovary", "Arrhenoblastoma of ovary", "Sertoli-Leydig Cell Tumor", "cell ovary sertoli-leydig tumor", "Sertoli-Leydig Neoplasm of Ovary", "Sertoli-Leydig neoplasm of ovary", "ovarian Sertoli-Leydig cell tumor", "Ovarian Sertoli-Leydig cell tumor", "Ovarian Sertoli-Leydig Cell Tumor", "Sertoli-Leydig cell tumor of ovary", "Sertoli-Leydig Cell Tumor of Ovary", "Ovarian Sertoli-Leydig cell tumour", "Sertoli-Leydig cell tumour of ovary", "Sertoli-Leydig Neoplasm of the Ovary", "ovarian Sertoli-Leydig cell neoplasm", "Sertoli-Leydig neoplasm of the ovary", "Ovarian Sertoli-Leydig Cell Neoplasm", "Sertoli-Leydig Cell Tumor of the Ovary", "Sertoli-leydig cell tumor of the ovary", "Sertoli-Leydig cell tumor of the ovary", "Sertoli-Leydig cell tumor of ovary (disorder)", "Sertoli-Leydig cell tumor of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian Sertoli-Leydig cell tumor", "shortest_name_length": 13}
{"curie": "MONDO:0000520", "names": ["parietal lobe ependymoma", "Parietal Lobe Ependymal Tumor", "parietal lobe ependymal tumor", "ependymal tumor of parietal lobe"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parietal lobe ependymal tumor", "shortest_name_length": 24}
{"curie": "UMLS:C1333779", "names": ["Gastric Lymphangioma", "Lymphangioma of Stomach", "Lymphangioma of the Stomach"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Lymphangioma", "shortest_name_length": 20}
{"curie": "MONDO:0032646", "names": ["CAKUT3", "congenital anomalies of kidney and urinary tract 3", "CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital anomalies of kidney and urinary tract 3", "shortest_name_length": 6}
{"curie": "MONDO:0100320", "names": ["post-COVID-19 disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "post-COVID-19 disorder", "shortest_name_length": 22}
{"curie": "UMLS:C5205912", "names": ["Prostate Granular Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Granular Cell Tumor", "shortest_name_length": 28}
{"curie": "UMLS:C4521647", "names": ["I", "Stage I Esophageal Adenocarcinoma", "Pathologic Stage I Esophageal Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage I Esophageal Adenocarcinoma AJCC v8", "shortest_name_length": 1}
{"curie": "MONDO:0002194", "names": ["vestibular papilloma", "Vestibular Papilloma", "Vulvar Squamous Papilloma", "vulvar squamous papilloma", "Vulvar Squamous Cell Papilloma", "mammalian vulva squamous papilloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vestibular papilloma", "shortest_name_length": 20}
{"curie": "UMLS:C3900098", "names": ["Myelodysplastic Syndrome", "Adult Myelodysplastic Syndrome", "adult myelodysplastic syndromes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Myelodysplastic Syndrome", "shortest_name_length": 24}
{"curie": "MONDO:0011079", "names": ["Patterson Lowry syndrome", "Patterson-Lowry rhizomelic dysplasia", "Rhizomelic dysplasia Patterson Lowry type", "rhizomelic dysplasia Patterson Lowry type", "rhizomelic dysplasia, Patterson-Lowry type", "RHIZOMELIC DYSPLASIA, PATTERSON-LOWRY TYPE", "Rhizomelic dysplasia, Patterson-Lowry type", "Rhizomelic Dysplasia, Patterson-Lowry Type", "Rhizomelic dysplasia of Patterson Lowry type", "Rhizomelic dysplasia of Patterson Lowry type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rhizomelic dysplasia, Patterson-Lowry type", "shortest_name_length": 24}
{"curie": "MONDO:0011225", "names": ["SCIDA", "RS-SCID", "ART-SCID", "artemis deficiency", "SCID, Athabascan type", "SCID, Athabaskan type", "Artemis-Deficient SCID", "SCID due to artemis deficiency", "SCID due to ARTEMIS deficiency", "SCID due to DCLRE1C deficiency", "SEVERE COMBINED IMMUNODEFICIENCY, PARTIAL", "severe combined immunodeficiency, partial", "Athabaskan Severe combined immunodeficiency", "ATHABASKAN SEVERE COMBINED IMMUNODEFICIENCY", "Athabaskan severe combined immunodeficiency", "Severe combined immunodeficiency Athabascan type", "SEVERE COMBINED IMMUNODEFICIENCY, ATHABASKAN-TYPE", "severe combined immunodeficiency, Athabascan type", "Severe combined immunodeficiency, Athabascan type", "severe combined immunodeficiency, Athabaskan type", "Severe combined immunodeficiency, Athabaskan type", "severe combined immunodeficiency, Athabaskan-type", "Severe Combined Immunodeficiency, Athabaskan Type", "Severe Combined Immunodeficiency, Athabascan Type", "SEVERE COMBINED IMMUNODEFICIENCY, ATHABASCAN-TYPE", "Artemis-Deficient Severe Combined Immunodeficiency", "DCLRE1C severe combined immunodeficiency (disease)", "severe combined immunodeficiency due to ARTEMIS deficiency", "severe combined immunodeficiency due to artemis deficiency", "severe combined immunodeficiency due to DCLRE1C deficiency", "Severe combined immunodeficiency due to ARTEMIS deficiency", "Severe combined immunodeficiency due to artemis deficiency", "Severe combined immunodeficiency due to DCLRE1C deficiency", "severe combined immunodeficiency with sensitivity to ionizing radiation", "SEVERE COMBINED IMMUNODEFICIENCY WITH SENSITIVITY TO IONIZING RADIATION", "Severe combined immunodeficiency with sensitivity to ionizing radiation", "severe combined immunodeficiency (disease) caused by mutation in DCLRE1C", "Severe combined immunodeficiency due to deoxyribonucleic acid cross-link repair protein 1c deficiency", "Severe combined immunodeficiency due to deoxyribonucleic acid cross-link repair protein 1c deficiency (disorder)", "SCID, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive, with sensitivity to ionizing radiation", "SCID, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-NEGATIVE, NK CELL-POSITIVE, WITH SENSITIVITY TO IONIZING RADIATION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe combined immunodeficiency due to DCLRE1C deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0003866", "names": ["liver osteosarcoma", "Liver Osteosarcoma", "hepatic osteosarcoma", "Hepatic Osteosarcoma", "osteosarcoma of liver", "Osteosarcoma of Liver", "Liver Osteogenic Sarcoma", "liver osteogenic sarcoma", "osteosarcoma of the liver", "Osteosarcoma of the Liver", "Hepatic Osteogenic Sarcoma", "hepatic osteogenic sarcoma", "osteogenic sarcoma of liver", "Osteogenic Sarcoma of Liver", "liver osteosarcoma (disease)", "osteogenic sarcoma of the liver", "Osteogenic Sarcoma of the Liver", "Liver Extraskeletal Osteosarcoma", "liver extraskeletal osteosarcoma", "hepatic extraskeletal osteosarcoma", "Hepatic Extraskeletal Osteosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "liver extraskeletal osteosarcoma", "shortest_name_length": 18}
{"curie": "MONDO:0054559", "names": ["CDG2Q", "CDGIIq", "CDG IIq", "CDGIIdq", "CDG Iiq", "COG2-CDG", "congenital disorder of glycosylation type IIq", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIq", "congenital disorder of glycosylation, type IIq", "COG2-related congenital disorder of glycosylation", "Component of oligomeric golgi complex 2-related congenital disorder of glycosylation", "COG2-CDG - component of oligomeric golgi complex 2 - congenital disorder of glycosylation", "Component of oligomeric golgi complex 2-related congenital disorder of glycosylation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital disorder of glycosylation, type IIq", "shortest_name_length": 5}
{"curie": "MONDO:0023227", "names": ["Gestagenic diabetes insipidus", "Gestational Diabetes Insipidus", "gestational diabetes insipidus", "diabetes insipidus gestational", "transient diabetes insipidus of pregnancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gestational diabetes insipidus", "shortest_name_length": 29}
{"curie": "MONDO:0043071", "names": ["Zazam Sheriff Phillips syndrome", "aniridia, lens luxation, mental retardation", "Aniridia, lens luxation, mental retardation", "aniridia, lens luxation, intellectual disability", "Aniridia, ectopia lentis, abnormal upper incisors and mental retardation", "aniridia, ectopia lentis, abnormal upper incisors and mental retardation", "aniridia, ectopia lentis, abnormal upper incisors and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Zazam Sheriff Phillips syndrome", "shortest_name_length": 31}
{"curie": "UMLS:C5205551", "names": ["High Risk Meningioma", "High-Risk Meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Risk Meningioma", "shortest_name_length": 20}
{"curie": "UMLS:C0262918", "names": ["extraocular muscle paresis", "EXTRAOCULAR MUSCLE PARESIS", "Extraocular Muscle Paresis", "Extraocular muscle paresis", "EXTRAOCULAR MUSCLE WEAKNESS", "Extraocular muscle weakness", "Paresis of extraocular muscles", "Paresis of extraocular muscles (disorder)", "extraocular muscle paresis (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extraocular Muscle Paresis", "shortest_name_length": 26}
{"curie": "MONDO:0003031", "names": ["cervix endometrial stromal tumor", "Cervical Endometrioid Stromal and Related Tumors", "Cervical Endometrioid Stromal and Related Neoplasms", "endometrioid stromal and related tumors of the cervix", "Endometrioid Stromal and Related Tumors of the Cervix", "endometrioid stromal and related neoplasms of the cervix", "Endometrioid Stromal and Related Neoplasms of the Cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometrioid stromal and related neoplasms of the cervix", "shortest_name_length": 32}
{"curie": "UMLS:C4745364", "names": ["Metastatic Oropharyngeal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Oropharyngeal Carcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0017486", "names": ["radial hemimelia, unilateral", "radial longitidinal meromelia, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radial hemimelia, unilateral", "shortest_name_length": 28}
{"curie": "UMLS:C4727277", "names": ["TEP1 Deficiency", "PTEN Deficiency", "PTEN1 Deficiency", "MMAC1 Deficiency", "PTEN Tyrosine Phosphatase Deficiency", "Phosphatase and Tensin Homolog Deficiency", "Mutated in Multiple Advanced Cancers 1 Deficiency", "Phosphatidylinositol 3,4,5-Trisphosphate 3-Phosphatase and Dual-Specificity Protein Phosphatase PTEN Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PTEN Deficiency", "shortest_name_length": 15}
{"curie": "MONDO:0005519", "names": ["pelvis renal cancer", "cancer pelvis renal", "renal pelvis cancer", "Renal Pelvis Cancer", "renal pelvis carcinoma", "Renal Pelvis Carcinoma", "cancer of renal pelvis", "Kidney Pelvis Carcinoma", "kidney pelvis carcinoma", "Renal pelvis cancer NOS", "carcinoma of renal pelvis", "Carcinoma of Renal Pelvis", "Carcinoma of Kidney Pelvis", "carcinoma of kidney Pelvis", "carcinoma of kidney pelvis", "kidney renal pelvis cancer", "Malignant Renal Pelvis Tumor", "carcinoma of the renal pelvis", "Carcinoma of the Renal Pelvis", "Carcinoma of the Kidney Pelvis", "carcinoma of the kidney pelvis", "malignant renal Pelvis neoplasm", "Malignant Tumor of Renal Pelvis", "Malignant Renal Pelvis Neoplasm", "Malignant tumor of renal pelvis", "malignant tumor of renal pelvis", "malignant renal pelvis neoplasm", "Malignant tumour of renal pelvis", "malignant neoplasm of renal pelvis", "Malignant neoplasm of renal pelvis", "Malignant Neoplasm of Renal Pelvis", "Malignant Tumor of the Renal Pelvis", "carcinoma of renal pelvis (diagnosis)", "Malignant Neoplasm of the Renal Pelvis", "Malignant tumor of renal pelvis (disorder)", "malignant neoplasm of renal pelvis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal pelvis carcinoma", "shortest_name_length": 19}
{"curie": "UMLS:C0549383", "names": ["hyperstimulation ovarian", "Ovarian hyperstimulation", "ovarian hyperstimulation", "OVARIAN HYPERSTIMULATION", "hyperstimulation; ovaries", "Hyperstimulation of ovaries", "Hyperstimulation of ovaries NOS", "Hyperstimulation of ovaries (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian hyperstimulation", "shortest_name_length": 24}
{"curie": "MONDO:0040654", "names": ["autosomal dominant oculocutaneous albinism", "oculocutaneous albinism, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant oculocutaneous albinism", "shortest_name_length": 42}
{"curie": "UMLS:C0433856", "names": ["Diffuse Brain Injury", "Diffuse brain injury", "diffuse brain injury", "Brain Injury, Diffuse", "Diffuse Brain Injuries", "brain; injury, diffuse", "injury; brain, diffuse", "Diffuse Cerebral Injury", "Brain Injuries, Diffuse", "Cerebral Injury, Diffuse", "Diffuse Cerebral Injuries", "Cerebral Injuries, Diffuse", "Diffuse Axonal Brain Injury", "diffuse axonal brain injury", "Diffuse axonal brain injury", "Diffuse brain injury (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brain Injuries, Diffuse", "shortest_name_length": 20}
{"curie": "UMLS:C0267558", "names": ["Drug and toxin-induced diarrhea", "Drug and toxin-induced diarrhoea"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drug and toxin-induced diarrhea", "shortest_name_length": 31}
{"curie": "MONDO:0003971", "names": ["gastric pylorus cancer", "Gastric Pylorus Cancer", "gastric pylorus carcinoma", "Gastric Pylorus Carcinoma", "cancer of gastric pylorus", "Cancer of Gastric Pylorus", "Carcinoma of Gastric Pylorus", "cancer of pylorus of stomach", "Cancer of Pylorus of Stomach", "carcinoma of gastric pylorus", "cancer of the gastric pylorus", "Cancer of the Gastric Pylorus", "Carcinoma of Pylorus of Stomach", "carcinoma of Pylorus of stomach", "carcinoma of pylorus of stomach", "Carcinoma of the Gastric Pylorus", "gastric pylorus (stomach) cancer", "Gastric Pylorus (Stomach) Cancer", "carcinoma of the gastric pylorus", "Cancer of the Pylorus of the Stomach", "cancer of the pylorus of the stomach", "carcinoma of the pylorus of the stomach", "Carcinoma of the Pylorus of the Stomach"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric pylorus carcinoma", "shortest_name_length": 22}
{"curie": "MONDO:0011876", "names": ["JAE", "EJA1", "juvenile absence epilepsy", "epilepsy juvenile absence", "susceptibility to juvenile absence epilepsy 1", "epilepsy, juvenile absence, susceptibility to, 1", "epilepsy, juvenile absence, susceptibility to, type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile absence epilepsy", "shortest_name_length": 3}
{"curie": "MONDO:0012224", "names": ["FEB6", "familial febrile seizures 6", "febrile seizures, familial, 6", "Seizures, Familial Febrile, 6", "FEBRILE SEIZURES, FAMILIAL, 6", "familial febrile convulsions 6", "Convulsions, Familial Febrile, 6", "CONVULSIONS, FAMILIAL FEBRILE, 6", "convulsions, familial febrile, 6", "FEBRILE CONVULSIONS, FAMILIAL, 6", "Febrile Convulsions, Familial, 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "febrile seizures, familial, 6", "shortest_name_length": 4}
{"curie": "UMLS:C4728180", "names": ["Contraindicated product prescribed"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Contraindicated product prescribed", "shortest_name_length": 34}
{"curie": "MONDO:0006504", "names": ["acquired metabolic disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired metabolic disease", "shortest_name_length": 26}
{"curie": "MONDO:0018571", "names": ["5q23 microdeletion syndrome", "contractures-developmental delay-Pierre Robin syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "contractures-developmental delay-Pierre Robin syndrome", "shortest_name_length": 27}
{"curie": "MONDO:0022151", "names": ["Chitty Hall Webb syndrome", "bowed tibiae, radial anomalies, osteopenia, multiple fractures and developmental delay"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chitty Hall Webb syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0008225", "names": ["NormoKPP", "normokalemic PP", "Periodic paralysis III", "periodic paralysis type 3", "Normokalemic Periodic Paralysis", "Normokalemic Periodic Paralyses", "normokalemic periodic paralysis", "Normokalemic periodic paralysis", "NORMOKALEMIC PERIODIC PARALYSIS", "Paralyses, Normokalemic Periodic", "Periodic Paralysis, Normokalemic", "Paralysis, Normokalemic Periodic", "Periodic Paralyses, Normokalemic", "Normokalaemic periodic paralysis", "Sodium-responsive periodic paralysis", "Familial normokalemic periodic paralysis", "normokalemic periodic paralysis syndrome", "Familial normokalaemic periodic paralysis", "potassium-sensitive normokalemic periodic paralysis", "Familial normokalemic periodic paralysis (disorder)", "normokalemic periodic paralysis syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "normokalemic periodic paralysis", "shortest_name_length": 8}
{"curie": "UMLS:C0431094", "names": ["Borderline Cystadenoma", "Borderline cystadenoma", "Borderline cystadenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline cystadenoma", "shortest_name_length": 22}
{"curie": "MONDO:0008017", "names": ["HMD", "Urban-Schosser-Spohn syndrome", "Urban Schosser Spohn syndrome", "Hereditary mucoepithelial dysplasia", "hereditary mucoepithelial dysplasia", "Mucoepithelial dysplasia, Hereditary", "mucoepithelial dysplasia, hereditary", "MUCOEPITHELIAL DYSPLASIA, HEREDITARY", "Hereditary mucoepithelial dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary mucoepithelial dysplasia", "shortest_name_length": 3}
{"curie": "UMLS:C2585653", "names": ["Persistent Atrial Fibrillation", "Persistent atrial fibrillation", "persistent atrial fibrillation", "Atrial fibrillation, persistent", "Atrial Fibrillation, Persistent", "Persistent Atrial Fibrillations", "Fibrillation, Persistent Atrial", "Fibrillations, Persistent Atrial", "Atrial Fibrillations, Persistent", "Persistent atrial fibrillation (disorder)", "persistent atrial fibrillation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Persistent atrial fibrillation", "shortest_name_length": 30}
{"curie": "UMLS:C4287847", "names": ["Vulvar Alveolar Rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Alveolar Rhabdomyosarcoma", "shortest_name_length": 32}
{"curie": "MONDO:0009224", "names": ["FIDD", "cretinism", "ENDEMIC CRETINISM", "Endemic cretinism", "endemic cretinism", "Endemic Cretinism", "Cretinism, endemic", "Cretinism, Endemic", "goitrous cretinism", "CRETINISM, ENDEMIC", "Fetal iodine syndrome", "fetal iodine syndrome", "Foetal iodine syndrome", "Endemic cretinism (disorder)", "Endemic hypothyroid cretinism", "Endemic cretinism - hypothyroid", "FETAL IODINE DEFICIENCY DISORDER", "Fetal iodine deficiency syndrome", "fetal iodine deficiency disorder", "Fetal Iodine Deficiency Disorder", "Fetal iodine syndrome (disorder)", "Foetal iodine deficiency syndrome", "Congenital iodine deficiency syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fetal iodine syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C4055115", "names": ["Dual Oxidase 2 Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dual Oxidase 2 Deficiency", "shortest_name_length": 25}
{"curie": "MONDO:0013441", "names": ["ATD4", "SRTD4", "ASPHYXIATING THORACIC DYSTROPHY 4", "asphyxiating thoracic dystrophy 4", "asphyxiating thoracic dystrophy type 4", "SHORT-RIB THORACIC DYSPLASIA 4 WITH OR WITHOUT POLYDACTYLY", "short-rib thoracic dysplasia 4 with or without polydactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "asphyxiating thoracic dystrophy 4", "shortest_name_length": 4}
{"curie": "MONDO:0030047", "names": ["MDBH", "MICROCEPHALY, DEVELOPMENTAL DELAY, AND BRITTLE HAIR SYNDROME", "microcephaly, developmental delay, and brittle hair syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly, developmental delay, and brittle hair syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C5206400", "names": ["Locally Advanced Unresectable Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Unresectable Breast Carcinoma", "shortest_name_length": 46}
{"curie": "MONDO:0012591", "names": ["OI5", "type V OI", "OI type 5", "OI type V", "OI, type 5", "OI, Type V", "OI, TYPE V", "OI5 Osteogenesis Imperfecta 5", "IFITM5 osteogenesis imperfecta", "osteogenesis imperfecta type 5", "Osteogenesis imperfecta type V", "Osteogenesis imperfecta type 5", "osteogenesis imperfecta type V", "Osteogenesis imperfecta, type 5", "Osteogenesis Imperfecta, Type V", "osteogenesis imperfecta, type V", "osteogenesis imperfecta, type 5", "OSTEOGENESIS IMPERFECTA, TYPE V", "Osteogenesis imperfecta type 5 (disorder)", "osteogenesis imperfecta type V (diagnosis)", "OI, type V Osteogenesis Imperfecta, Type V", "OI, type 5 Osteogenesis Imperfecta, Type 5", "Osteogenesis imperfecta with normal sclerae", "OI with calcification in interosseous membranes", "osteogenesis imperfecta caused by mutation in IFITM5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteogenesis imperfecta type 5", "shortest_name_length": 3}
{"curie": "MONDO:0013404", "names": ["S-adenosylhomocysteine hydrolase deficiency", "S-Adenosylhomocysteine Hydrolase Deficiency", "Deficiency of S-adenosylhomocysteine hydrolase", "Deficiency of S-adenosylhomocysteine hydrolase (disorder)", "hypermethioninemia with S-adenosylhomocysteine hydrolase deficiency", "HYPERMETHIONINEMIA WITH S-ADENOSYLHOMOCYSTEINE HYDROLASE DEFICIENCY", "Hypermethioninemia due to S-adenosylhomocysteine hydrolase deficiency", "hypermethioninemia due to S-adenosylhomocysteine hydrolase deficiency", "Hypermethioninemia with Deficiency of S-Adenosylhomocysteine Hydrolase", "hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase", "Hypermethioninaemia due to S-adenosylhomocysteine hydrolase deficiency", "psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency", "Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency", "Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency (disorder)", "Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase", "shortest_name_length": 43}
{"curie": "UMLS:C2982481", "names": ["Stage IV Hypopharyngeal Carcinoma", "Stage IV Hypopharyngeal Throat Cancer", "Stage IV Hypopharyngeal Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Hypopharyngeal Carcinoma AJCC v7", "shortest_name_length": 33}
{"curie": "MONDO:0013728", "names": ["RPRGL2", "F2 pregnancy loss, recurrent, susceptibility", "pregnancy loss, recurrent, susceptibility to, 2", "PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 2", "pregnancy loss, recurrent, susceptibility to, type 2", "pregnancy loss, recurrent, susceptibility caused by mutation in F2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pregnancy loss, recurrent, susceptibility to, 2", "shortest_name_length": 6}
{"curie": "UMLS:C1136321", "names": ["HIV Lipodystrophy Syndrome", "Lipodystrophy Syndrome, HIV", "HIV-Associated Lipodystrophy", "HIV Associated Lipodystrophy", "Lipodystrophy, HIV-Associated", "HIV-Associated Lipodystrophy Syndrome", "HIV-associated lipodystrophy syndrome", "HIV Associated Lipodystrophy Syndrome", "Lipodystrophy Syndrome, HIV-Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HIV-Associated Lipodystrophy Syndrome", "shortest_name_length": 26}
{"curie": "UMLS:C1336199", "names": ["Stage IIC Ovarian Cancer", "Ovarian Cancer Stage IIC", "Stage IIC Ovarian Carcinoma", "AJCC Stage IIC Ovarian Cancer", "FIGO Stage IIC Ovarian Cancer", "FIGO Stage IIC Cancer of Ovary", "FIGO Stage IIC Ovarian Carcinoma", "Stage IIC Ovarian Cancer AJCC v7", "Stage IIC Ovarian Cancer AJCC v6", "FIGO Stage IIC Carcinoma of Ovary", "FIGO Stage IIC Cancer of the Ovary", "Stage IIC Ovarian Epithelial Cancer", "FIGO Stage IIC Carcinoma of the Ovary", "Stage IIC Ovarian Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIC Ovarian Carcinoma", "shortest_name_length": 24}
{"curie": "MONDO:0015413", "names": ["median cleft of the upper lip and maxilla"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "median cleft of the upper lip and maxilla", "shortest_name_length": 41}
{"curie": "UMLS:C2981721", "names": ["stage IVB mycosis fungoides/Sezary syndrome", "Stage IVB Mycosis Fungoides and Sézary Syndrome", "Stage IVB Mycosis Fungoides and Sezary Syndrome", "stage IVB mycosis fungoides and Sezary syndrome AJCC v7", "Stage IVB Mycosis Fungoides and Sezary Syndrome AJCC v7", "Stage IVB Mycosis Fungoides and Sézary Syndrome AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Mycosis Fungoides and Sezary Syndrome AJCC v7", "shortest_name_length": 43}
{"curie": "UMLS:C0162679", "names": ["Leukemic infiltration", "Leukemic Infiltration", "Leukaemic infiltration", "Infiltration, Leukemic", "Leukemic Infiltrations", "Infiltrations, Leukemic", "Leukemic infiltration (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leukemic Infiltration", "shortest_name_length": 21}
{"curie": "MONDO:0030913", "names": ["MRD48", "autosomal dominant mental retardation 48", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 48", "mental retardation, autosomal dominant 48", "autosomal dominant intellectual disability 48", "intellectual disability, autosomal dominant 48", "autosomal dominant intellectual developmental disorder 48", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 48", "microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom", "Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 48", "shortest_name_length": 5}
{"curie": "MONDO:0001485", "names": ["atypical depression", "Atypical depression", "atypical; depression", "depression; atypical", "Atypical depressive disorder", "atypical depressive disorder", "Atypical depressive disorder (disorder)", "atypical depressive disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical depressive disorder", "shortest_name_length": 19}
{"curie": "MONDO:0012846", "names": ["GEFSP6", "GEFS+6", "GEFS, Type 6", "Gefs+, type 6", "GEFS+, TYPE 6", "generalized epilepsy with febrile seizures plus 6", "generalised epilepsy with febrile seizures plus 6", "generalized epilepsy with febrile seizures plus type 6", "generalised epilepsy with febrile seizures plus type 6", "Generalized Epilepsy With Febrile Seizures Plus, Type 6", "generalized epilepsy with febrile seizures plus, type 6", "GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "generalized epilepsy with febrile seizures plus, type 6", "shortest_name_length": 6}
{"curie": "MONDO:0043459", "names": ["Radiation disease", "Radiation disease, NOS", "Radiation-induced disorder", "radiation-induced disorder", "Radiation-Induced Disorder", "radiation exposure disorder", "radiation-induced Abnormality", "Radiation-Induced Abnormality", "Abnormality, Radiation-Induced", "Abnormality, radiation-induced", "Radiation-Induced Abnormalities", "radiation-induced abnormalities", "Radiation Induced Abnormalities", "radiation induced abnormalities", "Abnormalities, Radiation-Induced", "abnormalities, radiation induced", "Abnormalities, Radiation Induced", "disease (or disorder); radiation", "Disorder due to exposure to radiation", "Disorder caused by exposure to radiation", "Disorder due to exposure to ionising radiation", "Disorder due to exposure to ionizing radiation", "Disorder caused by exposure to ionising radiation", "Disorder caused by exposure to ionizing radiation", "Disorder caused by exposure to ionizing radiation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radiation-induced disorder", "shortest_name_length": 17}
{"curie": "UMLS:C3272482", "names": ["Ampulla of Vater MANEC", "Ampulla of Vater Mixed Adenoneuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ampulla of Vater Mixed Adenoneuroendocrine Carcinoma", "shortest_name_length": 22}
{"curie": "UMLS:C1698194", "names": ["anastomotic leak vagina", "Vaginal anastomotic leak", "Vaginal Anastomotic Leakage", "Vaginal anastomotic leak (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Anastomotic Leakage", "shortest_name_length": 23}
{"curie": "MONDO:0005876", "names": ["Nidovirales Infections", "Nidovirales infectious disease", "Nidovirales disease or disorder", "Nidovirales caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nidovirales infectious disease", "shortest_name_length": 22}
{"curie": "MONDO:0008734", "names": ["ADCC", "ADRENOCORTICAL CARCINOMA, PEDIATRIC", "hereditary adrenal cortex carcinoma", "Adrenocortical Carcinoma, Pediatric", "adrenocortical carcinoma, pediatric", "ADRENOCORTICAL CARCINOMA, HEREDITARY", "Adrenocortical Carcinoma, Hereditary", "adrenocortical carcinoma, hereditary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adrenocortical carcinoma, hereditary", "shortest_name_length": 4}
{"curie": "MONDO:0008428", "names": ["SOD", "CPHD5", "De Morsier Syndrome", "DE MORSIER SYNDROME", "De Morsier syndrome", "septooptic dysplasia", "Septooptic dysplasia", "SEPTOOPTIC DYSPLASIA", "Septooptic Dysplasia", "Septo optic dysplasia", "de Morsier's syndrome", "Septooptic Dysplasias", "Septo-Optic Dysplasia", "septo-optic dysplasia", "Dysplasia, Septooptic", "Septo-optic dysplasia", "septo-optic; dysplasia", "dysplasia; septo-optic", "Septo-optic dysplasia spectrum", "Septo-Optic Dysplasia Sequence", "Septo-optic dysplasia sequence", "septo-optic dysplasia sequence", "septo-optic dysplasia spectrum", "septo-optic dysplasia (diagnosis)", "PITUITARY HORMONE DEFICIENCY, COMBINED, 5", "pituitary hormone deficiency, combined, 5", "Septo-optic dysplasia sequence (disorder)", "Pituitary Hormone Deficiency, Combined, 5", "hypopituitarism and septooptic 'dysplasia'", "GROWTH HORMONE DEFICIENCY WITH PITUITARY ANOMALIES", "Growth hormone deficiency with pituitary anomalies", "Growth Hormone Deficiency With Pituitary Anomalies", "Septo-Optic Dysplasia with Growth Hormone Deficiency", "Septo Optic Dysplasia with Growth Hormone Deficiency", "septo-optic dysplasia with growth hormone deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "septooptic dysplasia", "shortest_name_length": 3}
{"curie": "UMLS:C1332978", "names": ["Lymphocyte-Rich Classical Hodgkin Lymphoma", "Childhood Lymphocyte-Rich Classic Hodgkin Lymphoma", "Childhood Lymphocyte Rich Classical Hodgkin Lymphoma", "Childhood Lymphocyte-Rich Classical Hodgkin Lymphoma", "Pediatric Lymphocyte Rich Classical Hodgkin's Disease", "Childhood Lymphocyte Rich Classical Hodgkin's Disease", "Pediatric Lymphocyte Rich Classical Hodgkin's Lymphoma", "Childhood Lymphocyte Rich Classical Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Lymphocyte-Rich Classic Hodgkin Lymphoma", "shortest_name_length": 42}
{"curie": "MONDO:0010222", "names": ["OS", "OSX", "XLOS", "GBBB", "GBBB1", "g syndrome", "G syndrome", "bbb syndrome", "BBG syndrome", "BBB syndrome", "GBBB syndrome", "BBBG syndrome", "BBB/G syndrome", "OPITZ SYNDROME", "opitz syndrome", "G/BBB syndrome", "Opitz Syndrome", "Opitz syndrome", "OGS1, FORMERLY", "GBBB1, FORMERLY", "BBBG1, FORMERLY", "opitz syndromes", "Opitz's syndrome", "Opitz GBBB syndrome", "OPITZ GBBB SYNDROME", "Opitz syndrome (OS)", "Opitz BBBG syndrome", "Opitz-Frias syndrome", "Opitz BBB/G syndrome", "Opitz G/BBB syndrome", "opitz-frias syndrome", "X-linked Opitz syndrome", "Opitz's (J.M.) syndrome", "Opitz-G Syndrome, Type I", "Opitz Syndrome, X-Linked", "Opitz syndrome, X-linked", "OPITZ SYNDROME, X-LINKED", "Opitz-G syndrome, type 1", "Opitz GBBB syndrome, type I", "Opitz Bbbg syndrome, type 1", "Opitz GBBB Syndrome, Type I", "Opitz GBBB syndrome, type 1", "Opitz BBBG Syndrome, Type I", "Opitz GBBB Syndrome, X-Linked", "OPITZ GBBB SYNDROME, X-LINKED", "X-linked Opitz BBB/G syndrome", "Opitz GBBB syndrome, X-linked", "X-linked Opitz G/BBB syndrome", "hypospadias-dysphagia syndrome", "Opitz G/BBB syndrome, X-linked", "X-Linked Opitz Syndrome (XLOS)", "X-linked Opitz syndrome (XLOS)", "Hypospadias-dysphagia syndrome", "oculo-genito-laryngeal syndrome", "Opitz-Frias syndrome (disorder)", "telecanthus-hypospadias syndrome", "TELECANTHUS-HYPOSPADIAS SYNDROME", "autosomal dominant Opitz syndrome", "hypertelorism-hypospadias syndrome", "Hypertelorism-hypospadias syndrome", "HYPERTELORISM-HYPOSPADIAS SYNDROME", "OPITZ-G SYNDROME, TYPE I, FORMERLY", "OPITZ GBBB SYNDROME, TYPE I, FORMERLY", "OPITZ BBBG SYNDROME, TYPE I, FORMERLY", "autosomal dominant Opitz syndrome (ADOS)", "Opitz GBBB syndrome, type I, X-linked recessive", "HYPERTELORISM WITH ESOPHAGEAL ABNORMALITY AND HYPOSPADIAS", "hypertelorism with esophageal Abnormality and hypospadias", "Hypertelorism-oesophageal abnormality-hypospadias syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked Opitz G/BBB syndrome", "shortest_name_length": 2}
{"curie": "MONDO:0012535", "names": ["Holoprosencephaly, recurrent infections, and monocytosis", "holoprosencephaly, recurrent infections, and monocytosis", "HOLOPROSENCEPHALY, RECURRENT INFECTIONS, AND MONOCYTOSIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "holoprosencephaly, recurrent infections, and monocytosis", "shortest_name_length": 56}
{"curie": "MONDO:0001502", "names": ["retroperitoneal cancer", "Retroperitoneal Cancer", "Retroperitoneal carcinoma", "retroperitoneal carcinoma", "Retroperitoneal Carcinoma", "retroperitoneum carcinoma", "carcinoma of Retroperitoneum", "carcinoma of retroperitoneum", "Carcinoma of Retroperitoneum", "retroperitoneal space carcinoma", "carcinoma of the retroperitoneum", "Carcinoma of the Retroperitoneum", "carcinoma of retroperitoneal space", "carcinoma of retroperitoneum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retroperitoneum carcinoma", "shortest_name_length": 22}
{"curie": "MONDO:0010196", "names": ["WS", "WRN", "Werner", "Pangeria", "Adult progeria", "Adult Progeria", "adult progeria", "WERNER SYNDROME", "werner syndrome", "adults progeria", "Werner Syndrome", "Progeria, Adult", "Werner syndrome", "syndrome werner", "Werners Syndrome", "Syndrome, Werner", "werners syndrome", "syndromes werner", "syndromes werners", "Syndrome, Werners", "Werner's Syndrome", "werner's syndrome", "Werner's syndrome", "syndromes werner's", "Syndrome, Werner's", "PROGERIA, OF ADULT", "Progeria of the adult", "Werner syndrome (disorder)", "Adult premature aging syndrome", "Adult Premature Aging Syndrome", "Adult premature ageing syndrome", "adult premature ageing syndrome", "Werner syndrome (adult progeria)", "Werner syndrome (adult progeria) (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Werner syndrome", "shortest_name_length": 2}
{"curie": "UMLS:C0272320", "names": ["Hereditary hypoproconvertinemia", "Hereditary Factor VII Deficiency", "Hereditary hypoproconvertinaemia", "hypoproconvertinemia; congenital", "hereditary factor VII deficiency", "Hereditary factor VII deficiency disease", "Hereditary factor VII deficiency syndrome", "Hereditary factor VII deficiency disease (disorder)", "clotting factor; deficiency, VII (congenital) (hereditary)", "deficiency; clotting factor, VII (congenital) (hereditary)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hereditary factor VII deficiency disease", "shortest_name_length": 31}
{"curie": "MONDO:0004159", "names": ["Mucinous cystadenocarcinoma, non-invasive", "pancreatic non-invasive mucinous cystadenocarcinoma", "Pancreatic Non-Invasive Mucinous Cystadenocarcinoma", "Mucinous cystadenocarcinoma, non-invasive (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic non-invasive mucinous cystadenocarcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0008954", "names": ["CG2", "PBD2A", "peroxisome biogenesis disorder 2A", "Peroxisome Biogenesis Disorder 2A", "peroxisome biogenesis disorder 2A (Zellweger)", "PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER)", "peroxisome biogenesis disorder, complementation group 2", "PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder 2A (Zellweger)", "shortest_name_length": 3}
{"curie": "MONDO:0006181", "names": ["GI carcinoma", "Carcinoma;digestive", "CARCINOMA GASTROINTESTINAL", "Digestive System Carcinoma", "GASTROINTESTINAL CARCINOMA", "Carcinoma gastrointestinal", "gastrointestinal carcinoma", "digestive system carcinoma", "Gastrointestinal carcinoma", "carcinoma of digestive system", "gastrointestinal system carcinoma", "Gastrointestinal System Carcinoma", "carcinoma of the digestive system", "gastrointestinal carcinoma (disease)", "Carcinoma of the Gastrointestinal System", "carcinoma of the gastrointestinal system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "digestive system carcinoma", "shortest_name_length": 12}
{"curie": "UMLS:C0600467", "names": ["Neurogenic Inflammation", "neurogenic inflammation", "Neurogenic Inflammations", "Inflammation, Neurogenic", "Inflammations, Neurogenic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neurogenic Inflammation", "shortest_name_length": 23}
{"curie": "UMLS:C1959609", "names": ["EROSION", "erosion", "Erosion", "Erosions", "Erosion lesion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Erosion lesion", "shortest_name_length": 7}
{"curie": "MONDO:0012244", "names": ["HPC5", "PROSTATE CANCER, HEREDITARY, 5", "Prostate Cancer, Hereditary, 5", "prostate cancer, hereditary, 5", "prostate cancer, hereditary, type 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate cancer, hereditary, 5", "shortest_name_length": 4}
{"curie": "MONDO:0007896", "names": ["M5", "AMoL", "AML M5", "FAB M5", "AML-M5", "FAB M5B", "monocytic leukemia", "Monocytic Leukemia", "Acute monocytic leukemia", "Acute Monocytic Leukemia", "leukemia monocytic acute", "acute monocytic leukemia", "Leukemia, Acute Monocytic", "leukemia, acute monocytic", "Monocytic Leukemia, Acute", "monocytic leukemia, acute", "Acute monocytic leukaemia", "acute monocytic leukaemia", "Acute monocytoid leukemia", "Monocytic leukemia, acute", "LEUKEMIA, ACUTE MONOCYTIC", "Acute Monocytic Leukemias", "Acute monoblastic leukemia", "Acute Monoblastic Leukemia", "Leukemia, Monocytic, Acute", "Acute monocytoid leukaemia", "acute monoblastic leukemia", "Monocytic Leukemias, Acute", "Monocytic leukaemia, acute", "Leukemias, Acute Monocytic", "monocytic; leukemia, acute", "Monoblastic leukaemia, NOS", "Myeloid Leukemia, Acute, M5", "Monoblastic Leukemia, Acute", "Acute Monoblastic Leukemias", "[M]Acute monocytic leukemia", "Acute monoblastic leukaemia", "[M]Acute monocytic leukaemia", "Leukemia, Monoblastic, Acute", "Leukemia, Myeloid, Acute, M5", "Monoblastic Leukemias, Acute", "Leukemias, Acute Monoblastic", "M5b - Acute monocytic leukemia", "leukemia, monocytic, malignant", "LEUKEMIA, MONOCYTIC, MALIGNANT", "FAB M5 (includes all variants)", "M5b - Acute monocytic leukaemia", "Schilling-Type Myeloid Leukemia", "Myeloid Leukemia, Schilling-Type", "Leukemia, Schilling-Type Myeloid", "acute monocytic leukemia, FAB M5", "Myeloid Leukemia, Schilling Type", "Leukemia, Myeloid, Schilling Type", "Acute monocytic leukemia, FAB M5b", "Leukemia, Myeloid, Schilling-Type", "acute monocytic leukemia (FAB M5B)", "acute myeloblastic leukemia type 5", "Acute Monocytic Leukemia (FAB M5b)", "acute monocytic leukemia (FAB M5b)", "Acute monocytic leukaemia, FAB M5b", "Acute Monocytic Leukemia (Fab M5B)", "acute monocytic leukemia, morphology", "acute monocytic leukemia (diagnosis)", "acute monoblastic/monocytic leukemia", "Acute monocytic leukemia, morphology", "M5b Acute differentiated monocytic leukemia", "Acute monocytic leukemia, FAB M5b (disorder)", "acute monocytic leukemia without mention of remission", "acute monocytic leukaemia without mention of remission", "acute monoblastic leukemia and acute monocytic leukemia", "acute Monoblastic Leukemia and acute Monocytic Leukemia", "acute monocytic leukemia, morphology (morphologic abnormality)", "Acute monocytic leukemia, morphology (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute monocytic leukemia", "shortest_name_length": 2}
{"curie": "MONDO:0010668", "names": ["MRSD", "CHRS", "Christian syndrome", "CHRISTIAN SYNDROME", "Christian Syndrome", "mental retardation-skeletal dysplasia", "skeletal dysplasia-intellectual disability syndrome", "mental retardation skeletal dysplasia abducens palsy", "skeletal dysplasia with intellectual disability syndrome", "Skeletal dysplasia with intellectual disability syndrome", "intellectual disability skeletal dysplasia abducens palsy", "mental retardation, skeletal dysplasia, and abducens palsy", "MENTAL RETARDATION, SKELETAL DYSPLASIA, AND ABDUCENS PALSY", "Mental Retardation, Skeletal Dysplasia, and Abducens Palsy", "X-linked skeletal dysplasia-intellectual disability syndrome", "intellectual disability, skeletal dysplasia, and abducens palsy", "Skeletal dysplasia with intellectual disability syndrome (disorder)", "skeletal dysplasia with intellectual disability syndrome (diagnosis)", "INTELLECTUAL DEVELOPMENTAL DISORDER, SKELETAL DYSPLASIA, AND ABDUCENS PALSY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skeletal dysplasia-intellectual disability syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C1167654", "names": ["Acute prerenal failure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute prerenal failure", "shortest_name_length": 22}
{"curie": "UMLS:C4527008", "names": ["Stage III Retroperitoneal Sarcoma", "Stage III Retroperitoneal Sarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Retroperitoneal Sarcoma AJCC v8", "shortest_name_length": 33}
{"curie": "MONDO:0017506", "names": ["thumb hypodactyly, unilateral", "thumb oligodactyly, unilateral", "congenital absence/hypoplasia of thumb, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital absence/hypoplasia of thumb, unilateral", "shortest_name_length": 29}
{"curie": "UMLS:C4528223", "names": ["Florid Follicular Hyperplasia PTLD", "Florid Follicular Hyperplasia Post-Transplant Lymphoproliferative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Florid Follicular Hyperplasia Post-Transplant Lymphoproliferative Disorder", "shortest_name_length": 34}
{"curie": "UMLS:C4288039", "names": ["Vaginal Large Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Large Cell Neuroendocrine Carcinoma", "shortest_name_length": 43}
{"curie": "UMLS:C0034531", "names": ["Experimental Radiation Injury", "Radiation Injury, Experimental", "Experimental Radiation Injuries", "Injuries, Experimental Radiation", "Radiation Injuries, Experimental"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radiation Injuries, Experimental", "shortest_name_length": 29}
{"curie": "MONDO:0001974", "names": ["Orbit Angioma", "orbit angioma", "orbit hemangioma", "Angioma of Orbit", "angioma of orbit", "Orbit Hemangioma", "Hemangioma of Orbit", "hemangioma of orbit", "Hemangioma of orbit", "Angioma of the Orbit", "Angioma of the orbit", "Haemangioma of orbit", "angioma of the orbit", "Hemangioma of the Orbit", "hemangioma of the orbit", "Hemangioma of orbit (disorder)", "hemangioma of orbit (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemangioma of orbit", "shortest_name_length": 13}
{"curie": "UMLS:C4526589", "names": ["Stage IIIA Thymic Epithelial Neoplasm AJCC v8", "Stage IIIA Thymus Epithelial Neoplasm AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Thymic Epithelial Neoplasm AJCC v8", "shortest_name_length": 45}
{"curie": "MONDO:0010975", "names": ["ARVD2", "ARVC2", "arrhythmogenic right ventricular dysplasia 2", "ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 2", "arrhythmogenic right ventricular cardiomyopathy 2", "arrhythmogenic right ventricular dysplasia type 2", "Arrhythmogenic Right Ventricular Cardiomyopathy 2", "familial arrhythmogenic right ventricular dysplasia 2", "ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 2", "arrhythmogenic right ventricular dysplasia, familial, 2", "Arrhythmogenic Right Ventricular Dysplasia, Familial, 2", "arrhythmogenic right ventricular dysplasia, familial, type 2", "RYR2 familial isolated arrhythmogenic right ventricular dysplasia", "Familial isolated arrhythmogenic ventricular dysplasia, classic form", "Familial isolated arrhythmogenic ventricular cardiomyopathy, classic form", "Familial isolated arrhythmogenic ventricular dysplasia, right dominant form", "Familial isolated arrhythmogenic ventricular cardiomyopathy, right dominant form", "familial isolated arrhythmogenic right ventricular dysplasia caused by mutation in RYR2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arrhythmogenic right ventricular dysplasia 2", "shortest_name_length": 5}
{"curie": "MONDO:0004301", "names": ["FIOS", "Osteofibrosarcoma", "Osteogenic Fibrosarcoma", "fibroblastic osteosarcoma", "Fibroblastic Osteosarcoma", "Fibroblastic osteosarcoma", "osteosarcoma; fibroblastic", "fibroblastic; osteosarcoma", "osteosarcoma, fibroblastic", "fibrosarcomatous osteosarcoma", "Fibrosarcomatous Osteosarcoma", "osteosarcoma, fibrosarcomatous", "Fibroblastic Osteogenic Sarcoma", "fibroblastic osteogenic sarcoma", "sarcoma, osteogenic fibroblastic", "osteogenic sarcoma, fibroblastic", "fibrosarcomatous osteogenic sarcoma", "Fibrosarcomatous Osteogenic Sarcoma", "Fibrosarcomatous Osteogenic sarcoma", "FIBROSARCOMA, OSTEOGENIC, MALIGNANT", "osteogenic sarcoma, fibrosarcomatous", "Fibroblastic osteosarcoma (morphologic abnormality)", "fibroblastic osteosarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibrosarcomatous osteosarcoma", "shortest_name_length": 4}
{"curie": "UMLS:C4683238", "names": ["Pathologic Stage II Retinoblastoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage II Retinoblastoma AJCC v8", "shortest_name_length": 42}
{"curie": "MONDO:0001501", "names": ["sarcoma retroperitoneal", "Retroperitoneal sarcoma", "Retroperitoneal Sarcoma", "retroperitoneal sarcoma", "retroperitoneal sarcomas", "sarcoma of retroperitoneum", "retroperitoneal space sarcoma", "sarcoma of retroperitoneal space", "Retroperitoneal sarcoma (disorder)", "sarcoma of retroperitoneum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retroperitoneal sarcoma", "shortest_name_length": 23}
{"curie": "MONDO:0006108", "names": ["BDA", "Cholangioma", "cholangioma", "cholangiomas", "Cholangiomas", "Cholangioadenoma", "Bile duct adenoma", "Bile Duct Adenoma", "bile duct adenoma", "Hepatocholangioma", "adenoma bile duct", "bile duct adenomas", "Adenoma, Bile Duct", "Bile Duct Adenomas", "bile duct; adenoma", "adenoma; bile duct", "CHOLANGIOMA, benign", "Adenomas, Bile Duct", "CHOLANGIOMA, BENIGN", "adenoma of bile duct", "Adenoma of Bile Duct", "adenoma of the bile duct", "Adenoma of the Bile Duct", "Cholangiocellular adenoma", "Cholangioadenoma (disorder)", "Hepatocholangiocellular Adenoma", "Hepatocholangiocellular adenoma", "bile duct adenoma (morphologic abnormality)", "Bile duct adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bile duct adenoma", "shortest_name_length": 3}
{"curie": "MONDO:0004924", "names": ["chronic canaliculitis", "chronic actinomycosis", "Chronic canaliculitis", "actinomycosis, chronic", "chronic; canaliculitis", "canaliculitis; chronic", "lacrimal canaliculitis chronic", "chronic lacrimal canaliculitis", "Chronic lacrimal canaliculitis", "Chronic lacrimal canaliculitis (disorder)", "chronic lacrimal canaliculitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic canaliculitis", "shortest_name_length": 21}
{"curie": "MONDO:0012902", "names": ["DFNA27", "autosomal dominant deafness 27", "deafness, autosomal dominant 27", "DEAFNESS, AUTOSOMAL DOMINANT 27", "autosomal dominant nonsyndromic deafness 27", "autosomal dominant nonsyndromic hearing loss 27", "autosomal dominant nonsyndromic deafness type 27"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 27", "shortest_name_length": 6}
{"curie": "UMLS:C3272539", "names": ["Small Intestinal Gangliocytic Paraganglioma", "Small Intestinal Gangliocytic Neuroendocrine Tumor", "Small Intestinal Mixed Ganglioneuroma-Neuroendocrine Neoplasm", "Small Intestinal Composite Gangliocytoma/Neuroma and Neuroendocrine Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Intestinal Composite Gangliocytoma/Neuroma and Neuroendocrine Tumor", "shortest_name_length": 43}
{"curie": "UMLS:C0855147", "names": ["Recurrent B Lymphoblastic Lymphoma", "Recurrent B-Lymphoblastic Lymphoma", "Relapsed Precursor B-Lymphoblastic Lymphoma", "Precursor B-lymphoblastic lymphoma recurrent", "Recurrent Precursor B-Lymphoblastic Lymphoma", "Precursor B-lymphoblastic lymphoma NOS recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Precursor B-lymphoblastic lymphoma recurrent", "shortest_name_length": 34}
{"curie": "UMLS:C1334441", "names": ["LUNG CANCER METASTATIC TO BRAIN", "Lung Carcinoma Metastatic to the Brain", "Lung Carcinoma Metastatic in the Brain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Carcinoma Metastatic in the Brain", "shortest_name_length": 31}
{"curie": "MONDO:0008034", "names": ["Muscular Dystrophy, Pseudohypertrophic, With Internalized Capillaries", "MUSCULAR DYSTROPHY, PSEUDOHYPERTROPHIC, WITH INTERNALIZED CAPILLARIES", "muscular dystrophy, pseudohypertrophic, with Internalized capillaries"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy, pseudohypertrophic, with Internalized capillaries", "shortest_name_length": 69}
{"curie": "UMLS:C3888532", "names": ["Vasculitic ulcer", "Vasculitic Ulcer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vasculitic ulcer", "shortest_name_length": 16}
{"curie": "MONDO:0021515", "names": ["benign ethmoid sinus tumor", "Benign Ethmoid Sinus Tumor", "Benign Ethmoidal Sinus Tumor", "benign ethmoidal sinus tumor", "ethmoid sinus benign neoplasm", "Benign Tumor of Ethmoid Sinus", "Benign Ethmoid Sinus Neoplasm", "benign tumor of ethmoid sinus", "benign ethmoid sinus neoplasm", "Benign tumor of ethmoid sinus", "Benign tumour of ethmoid sinus", "Benign Ethmoidal Sinus Neoplasm", "Benign Tumor of Ethmoidal Sinus", "benign tumor of ethmoidal sinus", "benign ethmoidal sinus neoplasm", "benign neoplasm of ethmoid sinus", "Benign Neoplasm of Ethmoid Sinus", "Benign Tumor of the Ethmoid Sinus", "benign tumor of the ethmoid sinus", "Benign Neoplasm of Ethmoidal Sinus", "Benign neoplasm of ethmoidal sinus", "benign neoplasm of ethmoidal sinus", "benign tumor of the ethmoidal sinus", "Benign Tumor of the Ethmoidal Sinus", "benign neoplasm of the ethmoid sinus", "Benign Neoplasm of the Ethmoid Sinus", "benign neoplasm of the ethmoidal sinus", "Benign Neoplasm of the Ethmoidal Sinus", "benign neoplasm of ethmoid sinus (diagnosis)", "Benign neoplasm of ethmoidal sinus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of ethmoidal sinus", "shortest_name_length": 26}
{"curie": "UMLS:C0862642", "names": ["Stage III Prostate Adenocarcinoma", "Adenocarcinoma of the prostate stage III", "Stage III Prostate Adenocarcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma of the prostate stage III", "shortest_name_length": 33}
{"curie": "UMLS:C3267086", "names": ["Hypotensive transfusion reaction", "Hypotensive Transfusion Reaction", "Transfusion Reaction, Hypotensive", "Reaction, Hypotensive Transfusion", "Transfusion Reactions, Hypotensive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypotensive Transfusion Reaction", "shortest_name_length": 32}
{"curie": "UMLS:C1527401", "names": ["Insulin Shock", "INSULIN SHOCK", "Insulin shock", "Shock insulin", "SHOCK INSULIN", "Shock, Insulin", "Insulin Reaction", "Hypoglycemic Shock"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Insulin Shock", "shortest_name_length": 13}
{"curie": "UMLS:C4054707", "names": ["Intermediate Osteoclastic Giant Cell-Rich Tumor of Bone", "Intermediate Osteoclastic Giant Cell-Rich Tumor of the Bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intermediate Osteoclastic Giant Cell-Rich Tumor of Bone", "shortest_name_length": 55}
{"curie": "UMLS:C1518315", "names": ["Nevus of Female Genitalia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nevus of Female Genitalia", "shortest_name_length": 25}
{"curie": "MONDO:0016847", "names": ["trisomy 1q", "Trisomy 1q", "1q+ syndrome", "Duplication 1q", "trisomy type 1q", "dup(1q) syndrome", "Partial Trisomy 1q", "partial trisomy 1q", "Trisomy 1q syndrome", "chromosome 1q trisomy", "1q duplication syndrome", "duplication 1q syndrome", "Trisomy 1q syndrome (disorder)", "Trisomy 1q syndrome (diagnosis)", "chromosome 1q duplication syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trisomy 1q", "shortest_name_length": 10}
{"curie": "MONDO:0033374", "names": ["DEE65", "EIEE65", "early infantile epileptic encephalopathy 65", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 65", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 65", "epileptic encephalopathy, early infantile, 65", "developmental and epileptic encephalopathy 65", "developmental and epileptic encephalopathy, 65"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 65", "shortest_name_length": 5}
{"curie": "MONDO:0045049", "names": ["hypermature cataract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypermature cataract", "shortest_name_length": 20}
{"curie": "MONDO:0019399", "names": ["neuromyotonia", "Isaac syndrome", "Isaacs' syndrome", "Isaac-Mertens syndrome", "Acquired Neuromyotonia", "acquired neuromyotonia", "Neuromyotonia, Acquired", "Isaac's-Merten's syndrome", "Quantal squander syndrome", "peripheral nerve hyperexcitability", "continuous muscle fiber activity syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Isaac syndrome", "shortest_name_length": 13}
{"curie": "UMLS:C2720436", "names": ["Pleural Fibrosis", "pleural fibrosis", "PLEURAL FIBROSIS", "pleura; fibrosis", "Pleural fibrosis", "fibrosis; pleura", "Fibrosis of pleura", "pleural fibrosis (diagnosis)", "Fibrosis of pleura (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fibrosis of pleura", "shortest_name_length": 16}
{"curie": "MONDO:0004042", "names": ["urethra inverted papilloma", "Urethra Inverted Papilloma", "urethral inverted papilloma", "Urethral Inverted Papilloma", "inverted papilloma of urethra", "Inverted Papilloma of Urethra", "inverted papilloma of the urethra", "Inverted papilloma of the urethra", "Inverted Papilloma of the Urethra"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urethra inverted papilloma", "shortest_name_length": 26}
{"curie": "MONDO:0012895", "names": ["DYT17", "torsion dystonia 17", "torsion dystonia type 17", "dystonia-17, primary torsion", "primary dystonia, DYT17 type", "Dystonia 17, Torsion, Autosomal Recessive", "dystonia 17, torsion, autosomal recessive", "DYSTONIA 17, TORSION, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "torsion dystonia 17", "shortest_name_length": 5}
{"curie": "UMLS:C0854822", "names": ["Stage I Anaplastic Large Cell Lymphoma", "Anaplastic Large Cell Lymphoma Stage I", "Ann Arbor Stage I Anaplastic Large Cell Lymphoma", "Anaplastic Large Cell Lymphoma T- and Null-Cell Types Stage I", "Ann Arbor Stage I Noncutaneous Anaplastic Large Cell Lymphoma", "Anaplastic large cell lymphoma T- and null-cell types stage I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Anaplastic Large Cell Lymphoma", "shortest_name_length": 38}
{"curie": "MONDO:0017087", "names": ["neurenteric cyst"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurenteric cyst", "shortest_name_length": 16}
{"curie": "MONDO:0030860", "names": ["HMN5C", "DHMN5C", "DSMAVC", "DHMN VC", "spinal muscular atrophy, distal, type 5C", "SPINAL MUSCULAR ATROPHY, DISTAL, TYPE VC", "NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VC", "neuropathy, distal hereditary motor, type VC", "NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VC", "neuronopathy, distal hereditary motor, type 5C"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuronopathy, distal hereditary motor, type 5C", "shortest_name_length": 5}
{"curie": "UMLS:C1518718", "names": ["Ovarian Insular Carcinoid Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Insular Carcinoid Tumor", "shortest_name_length": 31}
{"curie": "UMLS:C4329784", "names": ["Eiken Type Chondrodysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eiken Type Chondrodysplasia", "shortest_name_length": 27}
{"curie": "UMLS:C4525085", "names": ["Stage 0 Colorectal Cancer AJCC v8", "Stage 0 Colorectal Carcinoma AJCC v8", "Stage 0 Colorectal (Colon or Rectal) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Colorectal Cancer AJCC v8", "shortest_name_length": 33}
{"curie": "UMLS:C0347656", "names": ["injury penis", "wound; penis", "penis injury", "penis; wound", "Penis injury", "injury; penis", "penis; injury", "penis injuries", "injuries penis", "Injury of penis", "injury of penis", "Injuries of penis", "penile tissue injury", "Injury of penis (disorder)", "injury of penis (diagnosis)", "injury of penis (physical finding)", "injury of external genitalia male penis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of penis", "shortest_name_length": 12}
{"curie": "MONDO:0002912", "names": ["Brainstem Tumor", "brainstem tumor", "tumor brain stem", "Brainstem Tumors", "Brain Stem Tumor", "brainstem cancer", "brain stem tumor", "brainstem tumors", "brain stem cancer", "Tumor, Brain Stem", "brain stem tumors", "Brain Stem Tumors", "Brainstem Neoplasm", "Tumor of Brainstem", "Tumor of Brain Stem", "Neoplasm, Brainstem", "Brain Stem Neoplasm", "Brainstem Neoplasms", "cancer of brainstem", "Neoplasms, Brainstem", "Neoplasm, Brain Stem", "Brain Stem Neoplasms", "Neoplasms, Brain Stem", "Neoplasm of Brainstem", "neoplasm of brainstem", "Tumor of the Brainstem", "Neoplasm of Brain Stem", "neoplasm of brain stem", "Neoplasm of brain stem", "tumor of the brainstem", "Tumor of the Brain Stem", "Primary Brain Stem Tumor", "primary brain stem tumor", "primary brain Stem tumor", "Neoplasm of the Brainstem", "malignant brainstem tumor", "Malignant Brainstem Tumor", "Primary Brainstem Neoplasm", "malignant brain stem tumor", "Malignant Brain Stem Tumor", "Neoplasm of the Brain Stem", "Brainstem Neoplasm, Primary", "Primary Brainstem Neoplasms", "primary brain stem neoplasm", "Neoplasm, Primary Brainstem", "Primary Brain Stem Neoplasm", "Malignant Tumor of Brainstem", "Brainstem Neoplasms, Primary", "Primary Brain Stem Neoplasms", "Neoplasms, Primary Brainstem", "malignant brainstem neoplasm", "neoplasm of adult brain stem", "malignant tumor of brainstem", "Malignant Brainstem Neoplasm", "malignant tumor of brain stem", "Neoplasms, Brainstem, Primary", "Malignant Brain Stem Neoplasm", "Brain Stem Neoplasms, Primary", "malignant brain stem neoplasm", "Malignant Tumor of Brain Stem", "malignant neoplasm of brainstem", "Malignant Neoplasm of Brainstem", "Malignant neoplasm of brainstem", "Malignant Tumor of the Brainstem", "Malignant Neoplasm of Brain Stem", "malignant tumor of the brainstem", "malignant neoplasm of brain stem", "Malignant neoplasm of brain stem", "malignant tumor of the brain stem", "Malignant Tumor of the Brain Stem", "Neoplasm of brain stem (disorder)", "neoplasm of brainstem (diagnosis)", "malignant neoplasm of the brainstem", "Malignant Neoplasm of the Brainstem", "Malignant Neoplasm of the Brain Stem", "malignant neoplasm of the brain stem", "Malignant neoplasm of brainstem (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brainstem cancer", "shortest_name_length": 15}
{"curie": "MONDO:0023286", "names": ["graphitosis", "Graphitosis", "Graphite fibrosis", "graphite fibrosis", "Graphite lung disease", "carbon pneumoconiosis", "graphite lung disease", "Graphite pneumoconiosis", "graphite pneumoconiosis", "graphite; pneumoconiosis", "pneumoconiosis; graphite", "Graphite fibrosis of lung", "graphite fibrosis of lung", "Graphite fibrosis (of lung)", "pulmonary fibrosis graphite", "lung; fibrosis, due to graphite", "fibrosis; lung, due to graphite", "Graphite fibrosis of lung (disorder)", "Graphite fibrosis of lung (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "graphite pneumoconiosis", "shortest_name_length": 11}
{"curie": "UMLS:C1272352", "names": ["vitamin D3 deficiency", "Vitamin D3 deficiency", "vitamin d3 deficiency", "Vitamin D3 Deficiency", "d3 deficiencies vitamin", "Deficiency of vitamin D3", "deficiency of vitamin D3", "Deficiency of vitamin D>3<", "vitamin D3 deficiency (diagnosis)", "Deficiency of vitamin D<sub>3</sub>", "Deficiency of vitamin D3 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Deficiency of vitamin D3", "shortest_name_length": 21}
{"curie": "UMLS:C3647833", "names": ["Grade 3b", "grade 3B follicular lymphoma", "Follicular Lymphoma Grade 3b", "Follicular lymphoma grade 3b", "Grade 3b Follicular Lymphoma", "Follicular lymphoma, grade 3B", "Follicular lymphoma grade IIIb", "Follicular lymphoma grade 3b (disorder)", "grade 3B follicular lymphoma (diagnosis)", "Follicular non-Hodgkin lymphoma grade 3b", "Follicular lymphoma grade 3b (morphologic abnormality)", "malignant neoplasm nodular lymphoma follicular grade 3b"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "grade 3B follicular lymphoma", "shortest_name_length": 8}
{"curie": "MONDO:0008468", "names": ["SPDA2", "ankylosing spondylitis 2", "SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 2", "spondyloarthropathy, susceptibility to, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloarthropathy, susceptibility to, 2", "shortest_name_length": 5}
{"curie": "UMLS:C5447329", "names": ["SCID-RAG2", "RAG2 Deficiency", "Severe Combined Immunodeficiency due to RAG2 Deficiency", "Severe Combined Immunodeficiency, T cell-Negative, B cell-Negative, RAG2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Severe Combined Immunodeficiency due to RAG2 Deficiency", "shortest_name_length": 9}
{"curie": "MONDO:0013410", "names": ["SRXY6", "46XY sex reversal 6", "46,XY sex reversal 6", "46,XY SEX REVERSAL 6", "46,XY SEX reversal 6", "46,XY Sex reversal type 6", "46,XY SEX REVERSAL, PARTIAL OR COMPLETE, MAP3K1-RELATED", "46,XY Sex reversal, partial or complete, Map3K1-related", "46,XY sex reversal, partial or complete, MAP3K1-related", "46,XY gonadal dysgenesis, partial or complete, Map3K1-related", "46,XY GONADAL DYSGENESIS, PARTIAL OR COMPLETE, MAP3K1-RELATED", "46,XY gonadal dysgenesis, partial or complete, MAP3K1-related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XY sex reversal 6", "shortest_name_length": 5}
{"curie": "MONDO:0013433", "names": ["PSC", "Sclerosing Cholangitis", "sclerosing cholangitis", "primary sclerosing cholangitis", "Primary Sclerosing Cholangitis", "Primary sclerosing cholangitis", "cholangitis primary sclerosing", "Sclerosing Cholangitis, Primary", "Cholangitis, Primary Sclerosing", "cholangitis, primary sclerosing", "CHOLANGITIS, PRIMARY SCLEROSING", "Primary Sclerosing Cholangitides", "Sclerosing Cholangitides, Primary", "Cholangitides, Primary Sclerosing", "PSC - Primary sclerosing cholangitis", "Primary sclerosing cholangitis (disorder)", "primary sclerosing cholangitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary sclerosing cholangitis", "shortest_name_length": 3}
{"curie": "MONDO:0100458", "names": ["MECOM-associated syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MECOM-associated syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0002486", "names": ["LN", "LIN", "Breast LN", "lobular neoplasia", "Lobular neoplasia", "Lobular Neoplasia", "Breast Lobular Neoplasia", "lobular carcinoma in situ", "Lobular Intraepithelial Neoplasia", "lobular intraepithelial neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lobular neoplasia", "shortest_name_length": 2}
{"curie": "UMLS:C5667168", "names": ["Immunodeficiency-Related Lymphoproliferative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immunodeficiency-Related Lymphoproliferative Disorder", "shortest_name_length": 53}
{"curie": "UMLS:C1167709", "names": ["Epidermal necrosis", "epidermal necrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epidermal necrosis", "shortest_name_length": 18}
{"curie": "MONDO:0017339", "names": ["AREI", "ICHTHYOSIS EXFOLIATIVA", "ichthyosis exfoliativa", "Exfoliative ichthyosis", "exfoliative ichthyosis", "Ichthyosis Exfoliativa", "Ichthyosis exfoliativa", "ICHTHYOSIS BULLOSA OF SIEMENS-LIKE", "autosomal recessive exfoliative ichthyosis", "Autosomal recessive exfoliative ichthyosis", "ICHTHYOSIS, EXFOLIATIVE, AUTOSOMAL RECESSIVE", "Autosomal recessive exfoliative ichthyosis (disorder)", "ichthyosis congenital autosomal recessive exfoliative", "Autosomal recessive exfoliative ichthyosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exfoliative ichthyosis", "shortest_name_length": 4}
{"curie": "MONDO:0004988", "names": ["Breast Adenocarcinoma", "Breast adenocarcinoma", "adenocarcinoma breast", "breast adenocarcinoma", "mammary adenocarcinoma", "Mammary adenocarcinoma", "adenocarcinoma of breast", "Adenocarcinoma of breast", "Adenocarcinoma of Breast", "adenocarcinoma of the breast", "Adenocarcinoma of the Breast", "Adenocarcinoma of mammary gland", "Mammary adenocarcinoma (disorder)", "Adenocarcinoma of breast (disorder)", "adenocarcinoma of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast adenocarcinoma", "shortest_name_length": 21}
{"curie": "MONDO:0011805", "names": ["AS1", "ASRT1", "asthma, susceptibility to, 1", "PTGDR inherited susceptibility to asthma", "ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 1", "asthma-related traits, susceptibility to, 1", "asthma-related traits, susceptibility to, type 1", "inherited susceptibility to asthma caused by mutation in PTGDR"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "asthma-related traits, susceptibility to, 1", "shortest_name_length": 3}
{"curie": "UMLS:C0272577", "names": ["PELVIS FRACTURE OPEN", "open pelvic fracture", "Open Fracture of Pelvis", "Open fracture of pelvis", "open fracture of pelvis", "Open fracture of pelvis, NOS", "Open fracture of pelvis (disorder)", "Unspecified open fracture of pelvis", "Open unspecified fracture of pelvis", "open fracture of pelvis (diagnosis)", "Fracture of pelvis, unspecified, open"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Open fracture of pelvis", "shortest_name_length": 20}
{"curie": "MONDO:0003673", "names": ["apical myocardial infarction", "Apical Myocardial Infarction by ECG Finding", "Apical Myocardial Infarction by EKG Finding"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "apical myocardial infarction", "shortest_name_length": 28}
{"curie": "MONDO:0030689", "names": ["CMT1H", "HNARMD", "Charcot-Marie-Tooth neuropathy, IIA 1H", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 1H", "HEREDITARY MOTOR AND SENSORY NEUROPATHY, IH", "hereditary motor and sensory neuropathy, 1h", "Charcot-Marie-Tooth disease, demyelinating, IIA 1H", "CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1H", "neuropathy, hereditary, with or without age-related macular degeneration", "NEUROPATHY, HEREDITARY, WITH OR WITHOUT AGE-RELATED MACULAR DEGENERATION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease, demyelinating, IIA 1H", "shortest_name_length": 5}
{"curie": "UMLS:C2931189", "names": ["Neural crest tumor", "Neural crest-derived tumors"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neural crest tumor", "shortest_name_length": 18}
{"curie": "UMLS:C1336121", "names": ["Stage IA Ovarian Cancer", "Ovarian Cancer Stage IA", "AJCC Stage IA Ovarian Cancer", "FIGO Stage IA Ovarian Cancer", "FIGO Stage IA Cancer of Ovary", "Stage IA Ovarian Cancer AJCC v7", "Stage IA Ovarian Cancer AJCC v6", "FIGO Stage IA Ovarian Carcinoma", "FIGO Stage IA Carcinoma of Ovary", "FIGO Stage IA Cancer of the Ovary", "stage IA ovarian epithelial cancer", "Stage IA Ovarian Epithelial Cancer", "FIGO Stage IA Carcinoma of the Ovary", "Stage IA Ovarian Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Ovarian Cancer", "shortest_name_length": 23}
{"curie": "MONDO:0002534", "names": ["fallopian tube papilloma", "Fallopian Tube Papilloma", "Fallopian Tube Serous Papilloma", "fallopian tube serous papilloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fallopian tube papilloma", "shortest_name_length": 24}
{"curie": "UMLS:C1112517", "names": ["Tuberculous abscess", "Tuberculous Abscess", "tuberculous abscess", "abscess; tuberculous", "tuberculosis; abscess", "Tuberculous abscess (disorder)", "tuberculous abscess (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tuberculous abscess", "shortest_name_length": 19}
{"curie": "UMLS:C5556715", "names": ["HPV-Independent Vaginal Squamous Cell Carcinoma", "Human Papillomavirus-Independent Vaginal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Human Papillomavirus-Independent Vaginal Squamous Cell Carcinoma", "shortest_name_length": 47}
{"curie": "UMLS:C4329637", "names": ["Central Nervous System Myofibroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Myofibroblastoma", "shortest_name_length": 39}
{"curie": "MONDO:0013298", "names": ["dup(17)(q21.31)", "Dup(17)(q21.31)", "trisomy 17q21.31", "Trisomy 17q21.31", "17q21.31 microduplication syndrome", "CHROMOSOME 17q21.31 DUPLICATION SYNDROME", "chromosome 17q21.31 duplication syndrome", "17q21.31 microduplication syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 17q21.31 duplication syndrome", "shortest_name_length": 15}
{"curie": "UMLS:C0333276", "names": ["acute bleed", "BLEEDING ACUTE", "acute bleeding", "Acute bleeding", "acute blood loss", "Acute blood loss", "acute hemorrhage", "Acute hemorrhage", "Acute haemorrhage", "Acute hemorrhage (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute hemorrhage", "shortest_name_length": 11}
{"curie": "UMLS:C1699141", "names": ["Enterostomy Prolapse", "intestinal stoma prolapse", "Intestinal Stoma Prolapse", "Prolapse of intestinal stoma", "intestinal stoma prolapse (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal Stoma Prolapse", "shortest_name_length": 20}
{"curie": "MONDO:0100348", "names": ["NEDMILG", "NEDMILG, AR", "neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities", "NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, IMPAIRED LANGUAGE, AND GAIT ABNORMALITIES", "neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities", "shortest_name_length": 7}
{"curie": "UMLS:C0085082", "names": ["Fungemia", "FUNGEMIA", "fungemia", "Fungaemia", "fungaemia", "Fungemia NOS", "Fungemia, NOS", "Fungemia (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fungemia", "shortest_name_length": 8}
{"curie": "UMLS:C4684845", "names": ["PAS", "PIS", "PAIS", "Pulmonary Artery Sarcoma", "Pulmonary Intimal Sarcoma", "Pulmonary artery intimal sarcoma", "Pulmonary Artery Intimal Sarcoma", "Intimal Sarcoma of the Pulmonary Artery"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pulmonary Artery Intimal Sarcoma", "shortest_name_length": 3}
{"curie": "UMLS:C0521664", "names": ["Acute Confusional Migraine", "Acute confusional migraine", "Migraine, Acute Confusional", "Acute Confusional Migraines", "Migraines, Acute Confusional", "Acute confusional migraine (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Confusional Migraine", "shortest_name_length": 26}
{"curie": "UMLS:C4527160", "names": ["Cutaneous Melanoma by AJCC v8 Stage", "Melanoma of the Skin by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous Melanoma by AJCC v8 Stage", "shortest_name_length": 35}
{"curie": "MONDO:0001378", "names": ["urachus cancer", "cancer of urachus", "malignant urachus neoplasm", "Malignant tumor of urachus", "malignant tumor of urachus", "Malignant tumour of urachus", "malignant neoplasm of urachus", "Malignant neoplasm of urachus", "Malignant tumor of urachus (disorder)", "malignant neoplasm of urachus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urachus cancer", "shortest_name_length": 14}
{"curie": "MONDO:0017596", "names": ["CNS DLBCL", "DLBCL of the CNS", "primary DLBCL of the CNS", "Primary DLBCL of the CNS", "central nervous system diffuse large B-cell lymphoma", "Central Nervous System Diffuse Large B-Cell Lymphoma", "Diffuse large B-cell lymphoma of central nervous system", "large B-cell diffuse lymphoma of central nervous system", "diffuse large B-cell lymphoma of central nervous system", "diffuse large B-cell lymphoma of the central nervous system", "Diffuse large B-cell lymphoma of the central nervous system", "Diffuse large B-cell lymphoma of central nervous system (disorder)", "Primary Diffuse Large B-Cell Lymphoma of the Central Nervous System", "large B-cell diffuse lymphoma of central nervous system (diagnosis)", "primary diffuse large B-cell lymphoma of the central nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diffuse large B-cell lymphoma of the central nervous system", "shortest_name_length": 9}
{"curie": "MONDO:0014537", "names": ["NPHP19", "NEPHRONOPHTHISIS 19", "nephronophthisis 19", "nephronophthisis type 19", "DCDC2 nephronophthisis (disease)", "nephronophthisis (disease) caused by mutation in DCDC2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephronophthisis 19", "shortest_name_length": 6}
{"curie": "MONDO:0011120", "names": ["NTDFS", "NTD, folate-sensitive", "NTD, FOLATE-SENSITIVE", "spina bifida, folate-sensitive", "Spina Bifida, Folate-Sensitive", "SPINA BIFIDA, FOLATE-SENSITIVE", "Neural tube defect, folate-sensitive", "neural tube defects, folate-sensitive", "Neural Tube Defects, Folate-Sensitive", "NEURAL TUBE DEFECTS, FOLATE-SENSITIVE", "neural tube defects, susceptibility to", "neural tube defects, folate-sensitive, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neural tube defects, folate-sensitive", "shortest_name_length": 5}
{"curie": "UMLS:C5205254", "names": ["Colon NET G2", "Colon Neuroendocrine Tumor G2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colon Neuroendocrine Tumor G2", "shortest_name_length": 12}
{"curie": "MONDO:0008473", "names": ["Brachyolmia Type 2", "SED, Maroteaux type", "SED, MAROTEAUX TYPE", "brachyolmia Maroteaux type", "pseudo-Morquio syndrome type 2", "Pseudo-Morquio syndrome type 2", "PSEUDO-MORQUIO SYNDROME, TYPE 2", "pseudo-Morquio syndrome, type 2", "spondyloepiphyseal dysplasia of Maroteaux", "Spondyloepiphyseal dysplasia Maroteaux type", "spondyloepiphyseal dysplasia Maroteaux type", "Spondyloepiphyseal dysplasia, Maroteaux type", "Spondyloepiphyseal Dysplasia, Maroteaux Type", "spondyloepiphyseal dysplasia, Maroteaux type", "SPONDYLOEPIPHYSEAL DYSPLASIA, MAROTEAUX TYPE", "spondyloepimetaphyseal dysplasia, Maroteaux type", "Spondyloepiphyseal dysplasia Maroteaux type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepimetaphyseal dysplasia, Maroteaux type", "shortest_name_length": 18}
{"curie": "UMLS:C0862432", "names": ["Stage IV Bladder Urothelial Cancer", "Stage IV Bladder Urothelial Carcinoma", "Urothelial carcinoma bladder stage IV", "Bladder transitional cell carcinoma stage IV", "Stage IV Bladder Urothelial Carcinoma AJCC v7", "Stage IV Transitional Cell Carcinoma of Bladder", "Transitional cell carcinoma of the bladder stage IV", "Stage IV Transitional Cell Carcinoma of the Bladder", "Stage IV Urinary Bladder Transitional Cell Carcinoma", "Stage IV Transitional Cell Carcinoma of Urinary Bladder", "Stage IV Transitional Cell Carcinoma of the Urinary Bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder transitional cell carcinoma stage IV", "shortest_name_length": 34}
{"curie": "MONDO:0015642", "names": ["benign partial infantile seizures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign partial infantile seizures", "shortest_name_length": 33}
{"curie": "UMLS:C4682800", "names": ["Stage IA Testicular Cancer", "Stage IA Testicular Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Testicular Cancer AJCC v8", "shortest_name_length": 26}
{"curie": "MONDO:0019505", "names": ["4H syndrome", "hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0011603", "names": ["NM", "QSM", "IBM2", "DMRV", "HIBM", "Ibm2", "HIBM2", "GNE myopathy", "GNE Myopathy", "GNE MYOPATHY", "IBM2, FORMERLY", "Nonaka myopathy", "Nonaka Myopathy", "NONAKA MYOPATHY", "NONAKA DISTAL MYOPATHY", "Nonaka distal myopathy", "rimmed vacuole myopathy", "Rimmed Vacuole Myopathy", "Rimmed vacuole myopathy", "inclusion body myopathy 2", "Inclusion Body Myopathy 2", "Inclusion body myopathy 2", "quadriceps-sparing myopathy", "quadriceps sparing myopathy", "Quadriceps-sparing myopathy", "Distal myopathy, Nonaka type", "distal myopathy, Nonaka type", "Inclusion body myopathy type 2", "inclusion body myopathy type 2", "Hereditary Inclusion Body Myopathy", "Hereditary inclusion body myopathy", "distal myopathy with rimmed vacuoles", "Distal Myopathy with Rimmed Vacuoles", "Inclusion body myopathy 2 (disorder)", "Distal myopathy with rimmed vacuoles", "Myopathy, distal, with rimmed vacuoles", "myopathy, distal, with rimmed vacuoles", "Hereditary inclusion body myopathy type 2", "Quadricep sparing inclusion body myopathy", "hereditary inclusion body myopathy type 2", "Inclusion body myopathy quadriceps sparing", "INCLUSION BODY MYOPATHY, QUADRICEPS-SPARING", "inclusion body myopathy autosomal recessive", "Inclusion Body Myopathy, Quadriceps-Sparing", "inclusion body myopathy, quadriceps-sparing", "Inclusion body myopathy autosomal recessive", "inclusion body myopathy, autosomal recessive", "Inclusion Body Myopathy, Autosomal Recessive", "Inclusion body myopathy 2, autosomal recessive", "inclusion body myopathy 2, autosomal recessive", "MYOPATHY, DISTAL, WITH OR WITHOUT RIMMED VACUOLES", "myopathy, distal, with or without rimmed vacuoles", "INCLUSION BODY MYOPATHY 2, AUTOSOMAL RECESSIVE, FORMERLY", "INCLUSION BODY MYOPATHY, HEREDITARY, AUTOSOMAL RECESSIVE", "inclusion body myopathy, hereditary, autosomal recessive", "inclusion body myopathy 2, autosomal recessive, formerly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "GNE myopathy", "shortest_name_length": 2}
{"curie": "MONDO:0010857", "names": ["FTD", "Ftdp17", "PICK COMPLEX", "Pick Complex", "semantic dementia", "semantic variant PPA", "frontotemporal dementia", "Ftld with Tau inclusions", "dementia, frontotemporal", "Wilhelmsen-Lynch disease", "frontotemporal lobe dementia", "Pallidopontonigral Degeneration", "semantic primary progressive aphasia", "frontotemporal dementia with Parkinsonism", "dementia, frontotemporal, with Parkinsonism", "multiple system tauopathy with presenile dementia", "frontotemporal lobar Degeneration with Tau inclusions", "dementia, frontotemporal, with or without parkinsonism", "disinhibition-dementia-Parkinsonism-amyotrophy Complex"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "semantic dementia", "shortest_name_length": 3}
{"curie": "MONDO:0013547", "names": ["MC5DN3", "MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATP5E TYPE", "mitochondrial Complex 5 (ATP synthase) deficiency, Atp5E type", "mitochondrial complex V (ATP synthase) deficiency nuclear type 3", "mitochondrial complex V (ATP synthase) deficiency, nuclear type 3", "MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 3", "mitochondrial Complex 5 (ATP synthase) deficiency, nuclear type 3", "ATP5F1E mitochondrial proton-transporting ATP synthase complex deficiency", "mitochondrial proton-transporting ATP synthase complex deficiency caused by mutation in ATP5F1E"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex V (ATP synthase) deficiency nuclear type 3", "shortest_name_length": 6}
{"curie": "UMLS:C0334457", "names": ["Fascial fibroma", "Fascial Fibroma", "Fascial fibroma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fascial fibroma", "shortest_name_length": 15}
{"curie": "MONDO:0015473", "names": ["Van Benthem-Driessen-Hanveld syndrome", "cryptorchidism arachnodactyly intellectual deficit", "cryptorchidism-arachnodactyly-intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cryptorchidism-arachnodactyly-intellectual disability syndrome", "shortest_name_length": 37}
{"curie": "UMLS:C5419190", "names": ["Advanced Sarcomatoid Renal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Sarcomatoid Renal Cell Carcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0009939", "names": ["Pulmonic stenosis and congenital nephrosis", "Pulmonic Stenosis and Congenital Nephrosis", "pulmonic stenosis and congenital nephrosis", "PULMONIC STENOSIS AND CONGENITAL NEPHROSIS", "Pulmonic stenosis and congenital nephrosis (disorder)", "Pulmonic stenosis and congenital nephrosis (diagnosis)", "renal disorders pulmonic stenosis and congenital nephrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonic stenosis and congenital nephrosis", "shortest_name_length": 42}
{"curie": "MONDO:0008530", "names": ["Lobodontia", "LOBODONTIA", "teeth, odd shapes of", "TEETH, ODD SHAPES OF", "Teeth, Odd Shapes Of", "CONICAL TEETH, MULTIPLE", "Conical Teeth, Multiple", "conical teeth, multiple"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "teeth, odd shapes of", "shortest_name_length": 10}
{"curie": "MONDO:0030057", "names": ["NEDJED", "neurodevelopmental, jaw, eye, and digital syndrome", "NEURODEVELOPMENTAL, JAW, EYE, AND DIGITAL SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental, jaw, eye, and digital syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0012249", "names": ["FCC2", "COCA2", "HNPCC2", "LYNCH2", "Lynch 2 syndrome", "Lynch 2 Syndrome", "Lynch Syndrome 2", "LYNCH SYNDROME 2", "Lynch syndrome 2", "Lynch Syndrome II", "Lynch syndrome II", "Lynch syndrome II (diagnosis)", "Lynch cancer family syndrome 2", "Lynch Cancer Family Syndrome II", "familial nonpolyposis colon cancer type 2", "familial non-polyposis colon cancer type 2", "Familial Non-Polyposis Colon Cancer Type 2", "colon cancer, familial nonpolyposis, type 2", "Colon Cancer, Familial Nonpolyposis, Type 2", "COLON CANCER, FAMILIAL NONPOLYPOSIS, TYPE 2", "Hereditary non-polyposis colon cancer type 2", "Hereditary Non-Polyposis Colon Cancer Type 2", "hereditary nonpolyposis colorectal cancer type 2", "Hereditary Nonpolyposis Colorectal Cancer Type 2", "Hereditary nonpolyposis colorectal cancer type 2", "colorectal cancer, hereditary nonpolyposis, type 2", "Colorectal Cancer, Hereditary Nonpolyposis, Type 2", "COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lynch syndrome 2", "shortest_name_length": 4}
{"curie": "MONDO:0007787", "names": ["HTC1", "HTC 1", "Ambras syndrome", "AMBRAS SYNDROME", "HYPERTRICHOSIS, CONGENITAL GENERALIZED", "hypertrichosis, congenital generalized", "Ambras type hypertrichosis universalis congenita", "hypertrichosis universalis congenita Ambras type", "Hypertrichosis universalis congenita Ambras type", "HYPERTRICHOSIS UNIVERSALIS CONGENITA, AMBRAS TYPE", "Hypertrichosis Universalis Congenita, Ambras Type", "hypertrichosis universalis congenita, Ambras type", "congenital generalized hypertrichosis, Ambras type", "Congenital generalized hypertrichosis, Ambras type", "HYPERTRICHOSIS UNIVERSALIS CONGENITA, AMBRAS TYPE (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ambras type hypertrichosis universalis congenita", "shortest_name_length": 4}
{"curie": "UMLS:C0266508", "names": ["Rachischises", "Rachischisis", "rachischisis", "Rachischisis (disorder)", "Rachischisis (diagnosis)", "congenital spinal anomaly spina bifida rachischisis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rachischisis", "shortest_name_length": 12}
{"curie": "UMLS:C2930618", "names": ["Intersex Condition", "Condition, Intersex", "Intersex Conditions", "Conditions, Intersex"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intersex Conditions", "shortest_name_length": 18}
{"curie": "MONDO:0014399", "names": ["ATLD2", "ataxia-telangiectasia-like disorder 2", "ATAXIA-TELANGIECTASIA-LIKE DISORDER 2", "ataxia-telangiectasia-like disorder type 2", "PCNA-related progressive neurodegenerative photosensitivity syndrome", "Proliferating cell nuclear antigen-related progressive neurodegenerative photosensitivity syndrome", "Proliferating cell nuclear antigen-related progressive neurodegenerative photosensitivity syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ataxia-telangiectasia-like disorder 2", "shortest_name_length": 5}
{"curie": "MONDO:0017917", "names": ["maternally-inherited SPG", "maternally-inherited spastic paraplegia", "MT-ATP6-related mitochondrial spastic paraplegia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maternally-inherited spastic paraplegia", "shortest_name_length": 24}
{"curie": "UMLS:C5555827", "names": ["Peritoneal Inclusion Cyst"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peritoneal Inclusion Cyst", "shortest_name_length": 25}
{"curie": "UMLS:C1336942", "names": ["Vaginal Rhabdomyoma", "Rhabdomyoma of Vagina", "Rhabdomyoma of the Vagina"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Rhabdomyoma", "shortest_name_length": 19}
{"curie": "MONDO:0002319", "names": ["phosphorus disorder", "Phosphorus disorder", "Phosphorus Disorders", "phosphorus metabolic disorder", "phosphorus metabolism disease", "Phosphorus Metabolic Disorder", "phosphorus; metabolic disorder", "Phosphorus Metabolism Disorder", "phosphorus metabolism disorder", "Phosphorus metabolism disorder", "metabolic disorder; phosphorus", "Metabolism Disorder, Phosphorus", "Phosphorus Metabolism Disorders", "Disorder, Phosphorus Metabolism", "Phosphorus metabolism disorders", "Disorders, Phosphorus Metabolism", "Metabolism Disorders, Phosphorus", "Disorder of phosphorus metabolism", "disorder of phosphorus metabolism", "Phosphorus--Metabolism--Disorders", "disorders of phosphorus metabolism", "Phosphorus metabolism disorder NOS", "Disorders of phosphorus metabolism", "Disorder of phosphorus metabolism, NOS", "Disorder of phosphorus metabolism (disorder)", "disorder of phosphorus metabolism (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phosphorus metabolism disease", "shortest_name_length": 19}
{"curie": "MONDO:0001205", "names": ["hypersecretion glaucoma", "Hypersecretion glaucoma", "hypersecretion; glaucoma", "glaucoma; hypersecretion", "Hypersecretion glaucoma (disorder)", "hypersecretion glaucoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypersecretion glaucoma", "shortest_name_length": 23}
{"curie": "UMLS:C0410000", "names": ["Overlap syndrome", "Overlap Syndrome", "overlap syndrome", "OVERLAP SYNDROME", "overlap syndromes", "overlaps syndrome", "overlapping syndrome", "Overlap syndrome (disorder)", "overlap syndromes (diagnosis)", "systemic involvement connective tissue overlap syndromes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Overlap syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0022780", "names": ["cleft lip palate pituitary deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleft lip palate pituitary deficiency", "shortest_name_length": 37}
{"curie": "UMLS:C2937222", "names": ["Ulcerative proctitis", "Proctitis ulcerative", "proctitis ulcerative", "ulcerative proctitis", "Idiopathic proctitis", "Ulcerative Proctitis", "ULCERATIVE PROCTITIS", "PROCTITIS ULCERATIVE", "proctitis; ulcerative", "proctitis ulceratives", "ulcerative; proctitis", "IP - Idiopathic proctitis", "Chronic ulcerative proctitis", "Ulcerative (chronic) proctitis", "ulcerative proctitis (diagnosis)", "Ulcerative (chronic) proctitis NOS", "Ulcerative colitis confined to rectum", "Chronic ulcerative proctitis (disorder)", "UC - Ulcerative colitis confined to rectum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic ulcerative proctitis", "shortest_name_length": 20}
{"curie": "MONDO:0010562", "names": ["Atresia coli", "colon atresia", "Colon Atresia", "colon; atresia", "atresia; colon", "Colonic Atresia", "COLONIC ATRESIA", "colonic atresia", "Colonic atresia", "Atresia of colon", "atresia of colon", "Atresia of Colon", "atresia; bowel, large", "bowel; atresia, large", "Large intestinal atresia", "colonic atresia (disease)", "Congenital Atresia of Colon", "Congenital atresia of colon", "congenital atresia of colon", "Atresia of the large intestine", "Congenital atresia of colon (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colonic atresia", "shortest_name_length": 12}
{"curie": "UMLS:C1518004", "names": ["Low Grade B-Cell Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Grade B-Cell Non-Hodgkin's Lymphoma", "shortest_name_length": 39}
{"curie": "UMLS:C4054913", "names": ["Fusion-Negative Rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fusion-Negative Rhabdomyosarcoma", "shortest_name_length": 32}
{"curie": "MONDO:0003546", "names": ["IIIrd nerve disorder", "oculomotor nerve disease", "Oculomotor nerve disease", "Oculomotor Nerve Diseases", "Oculomotor nerve disorder", "Oculomotor Nerve Disorder", "disorder oculomotor nerve", "n.oculomotorius; disorder", "oculomotor nerve disorder", "disease of oculomotor nerve", "Disorder of cranial nerve 3", "Third cranial nerve disease", "third cranial nerve disease", "Disorder of oculomotor nerve", "third cranial nerve disorder", "Third cranial nerve disorder", "disorder of oculomotor nerve", "Oculomotor nerve disease, NOS", "Oculomotor nerve disorder, NOS", "Third cranial nerve disease, NOS", "Third cranial nerve disorder, NOS", "Oculomotor nerve disease or syndrome", "oculomotor nerve disease or disorder", "Third cranial nerve disease (disorder)", "disease or disorder of oculomotor nerve", "Third cranial nerve disease or syndrome", "disease (or disorder); nerve, oculomotor", "disorder of oculomotor nerve (diagnosis)", "cranial nerve; disorder, third (oculomotor)", "disease (or disorder); cranial nerve, third (oculomotor)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "third cranial nerve disorder", "shortest_name_length": 20}
{"curie": "UMLS:C0151510", "names": ["ADRENAL CORTEX ATROPHY", "ATROPHY ADRENAL CORTEX", "Atrophy adrenal cortex", "Adrenocortical atrophy", "Adrenal cortex atrophy", "Atrophy of adrenal cortex", "Atrophy of adrenal cortex (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atrophy of adrenal cortex", "shortest_name_length": 22}
{"curie": "UMLS:C0751183", "names": ["Parietal Region Trauma", "Trauma, Parietal Region", "Region Trauma, Parietal", "Parietal Region Traumas", "Region Traumas, Parietal", "Traumas, Parietal Region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parietal Region Trauma", "shortest_name_length": 22}
{"curie": "UMLS:C5239392", "names": ["Nasal Cavity Exophytic Papilloma", "Nasal Cavity Exophytic Schneiderian Papilloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasal Cavity Exophytic Papilloma", "shortest_name_length": 32}
{"curie": "UMLS:C4552676", "names": ["Stage I", "Stage I Renal Cell Cancer", "Stage I Renal Cell Cancer AJCC v8", "Stage I Renal Cell Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Renal Cell Cancer AJCC v8", "shortest_name_length": 7}
{"curie": "MONDO:0001241", "names": ["Transient neonatal neutropenia", "transient neonatal neutropenia", "neutropenia transient neonatal", "Transient neonatal neutropenia (disorder)", "Transient neonatal neutropenia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transient neonatal neutropenia", "shortest_name_length": 30}
{"curie": "MONDO:0033368", "names": ["DEE59", "EIEE59", "infantile epileptic encephalopathy 59", "early infantile epileptic encephalopathy 59", "epileptic encephalopathy, early infantile, 59", "developmental and epileptic encephalopathy 59", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 59", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 59", "developmental and epileptic encephalopathy, 59"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 59", "shortest_name_length": 5}
{"curie": "MONDO:0014993", "names": ["MFM8", "myofibrillar myopathy 8", "myopathy, myofibrillar, 8", "MYOPATHY, MYOFIBRILLAR, 8", "myopathy, myofibrillar, type 8", "PYROXD1 myofibrillar myopathy (disease)", "myofibrillar myopathy (disease) caused by mutation in PYROXD1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myofibrillar myopathy 8", "shortest_name_length": 4}
{"curie": "UMLS:C0334252", "names": ["Microinvasive Squamous Cell Carcinoma", "microinvasive squamous cell carcinoma", "Microinvasive squamous cell carcinoma", "Squamous cell carcinoma, microinvasive", "Squamous cell carcinoma, micro-invasive", "microinvasive squamous cell carcinoma (diagnosis)", "Squamous cell carcinoma, microinvasive (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Squamous cell carcinoma, microinvasive", "shortest_name_length": 37}
{"curie": "UMLS:C5555431", "names": ["T-Cell Lymphoproliferative Disorder", "T/NK-Cell Lymphoproliferative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T/NK-Cell Lymphoproliferative Disorder", "shortest_name_length": 35}
{"curie": "UMLS:C4744803", "names": ["Thyroid Gland Rosai-Dorfman Disease", "Thyroid Gland Sinus Histiocytosis with Massive Lymphadenopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Rosai-Dorfman Disease", "shortest_name_length": 35}
{"curie": "UMLS:C0151435", "names": ["Enteropathic arthritis", "Arthritis enteropathic", "arthritis enteropathic", "ENTEROPATHIC ARTHRITIS", "Enteropathic Arthritis", "enteropathic arthritis", "arthritis of inflammatory bowel disease", "Arthritis due to inflammatory bowel disease", "arthritis of inflammatory bowel disease (diagnosis)", "Arthritis due to inflammatory bowel disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Enteropathic arthritis", "shortest_name_length": 22}
{"curie": "UMLS:C1332518", "names": ["Appendix Mucinous Cystadenoma", "Mucinous Appendix Cystadenoma", "Colloid Cystadenoma of Appendix", "Colloid Appendiceal Cystadenoma", "Mucinous Cystadenoma of Appendix", "Mucinous Appendiceal Cystadenoma", "Colloidal Cystadenoma of Appendix", "Colloid Cystadenoma of the Appendix", "Mucinous Cystadenoma of the Appendix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Appendix Mucinous Cystadenoma", "shortest_name_length": 29}
{"curie": "UMLS:C5401381", "names": ["Periapical COD", "Periapical Osseous Dysplasia", "Periapical cemento-osseous dysplasia", "Periapical Cemento-Osseous Dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Periapical Cemento-Osseous Dysplasia", "shortest_name_length": 14}
{"curie": "MONDO:0023157", "names": ["fibular hypoplasia scapulo pelvic dysplasia absent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibular hypoplasia scapulo pelvic dysplasia absent", "shortest_name_length": 50}
{"curie": "MONDO:0000432", "names": ["immunocytoma", "Immunocytoma", "Plasmacytic lymphoma", "Lymphoma, Plasmacytic", "lymphoma, plasmacytic", "lymphoma; plasmacytic", "plasmacytic; lymphoma", "Lymphoplasmacytic Lymphoma", "Lymphoplasmacytic lymphoma", "lymphoplasmacytic lymphoma", "Lymphoplasmacytoid Lymphoma", "lymphoplasmacytoid lymphoma", "lymphoplasmacytoid; lymphoma", "lymphoma; lymphoplasmacytoid", "Malignant lymphoma, plasmacytoid", "malignant lymphoplasmacytic lymphoma", "Immunocytoma, Lymphoplasmacytic Type", "Immunocytoma, lymphoplasmacytic type", "Malignant lymphoma, lymphoplasmacytic", "Malignant lymphoma - lymphoplasmacytic", "Malignant lymphoma, lymphoplasmacytoid", "lymphoma, lymphoplasmacytic, malignant", "LYMPHOMA, LYMPHOPLASMACYTIC, MALIGNANT", "Diffuse lymphosarcoma, lymphoplasmacytic", "Malignant lymphoplasmacytoid type lymphoma", "Malignant lymphoma, lymphoplasmacytoid type", "malignant neoplasm lymphoma lymphoplasmacytic", "[M]Malignant lymphoma, lymphoplasmacytoid type", "malignant lymphoplasmacytic lymphoma (diagnosis)", "Malignant lymphoma - lymphoplasmacytic (disorder)", "Diffuse lymphosarcoma with plasmacytoid differentiation", "Lymphoplasmacytic lymphoma (Waldenstrom macroglobulinemia)", "lymphoplasmacytic lymphoma (Waldenstrom macroglobulinemia)", "Malignant lymphoma, lymphoplasmacytic (morphologic abnormality)", "Malignant lymphoma, lymphocytic, with plasmacytoid differentiation, diffuse"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphoplasmacytic lymphoma", "shortest_name_length": 12}
{"curie": "MONDO:0030706", "names": ["trichomonal cystitis", "Trichomonas Cystitis", "Trichomonas cystitis", "Trichomonal cystitis", "trichomoniasis of bladder", "cystitis in trichomoniasis", "Cystitis in trichomoniasis", "Trichomonas vaginalis cystitis", "Trichomonal cystitis (disorder)", "cystitis; trichomonal (manifestation)", "Trichomonas vaginalis caused cystitis", "trichomonal; cystitis (manifestation)", "trichomoniasis of bladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Trichomonas cystitis", "shortest_name_length": 20}
{"curie": "MONDO:0004383", "names": ["adult CNS germinoma", "Adult CNS Germinoma", "Germinoma of Adult CNS", "germinoma of adult CNS", "Germinoma of the Adult CNS", "germinoma of the adult CNS", "central nervous system germinoma", "Central Nervous System Germinoma", "adult central nervous system germinoma", "Adult Central Nervous System Germinoma", "Germinoma of Adult Central Nervous System", "germinoma of adult central nervous system", "central nervous system germinoma of adults", "Germinoma of the Adult Central Nervous System", "germinoma of the adult central nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult central nervous system germinoma", "shortest_name_length": 19}
{"curie": "MONDO:0009997", "names": ["RBS", "Sc Syndrome", "SC syndrome", "SC phocomelia", "robert syndrome", "syndrome robert", "ROBERTS SYNDROME", "Roberts Syndrome", "roberts syndrome", "Roberts syndrome", "Robert's syndrome", "robert's syndrome", "Roberts syndrome (RS)", "SC Phocomelia Syndrome", "Sc Phocomelia Syndrome", "SC PHOCOMELIA SYNDROME", "SC phocomelia syndrome", "pseudothalidomide syndrome", "Pseudothalidomide Syndrome", "Pseudothalidomide syndrome", "Appelt-Gerken-Lenz syndrome", "Appelt-Gerken-Lenz Syndrome", "SC-pseudothalidomide syndrome", "Sc Pseudothalidomide Syndrome", "SC pseudothalidomide syndrome", "SC PSEUDOTHALIDOMIDE SYNDROME", "Roberts-SC Phocomelia Syndrome", "Roberts-Sc Phocomelia Syndrome", "Roberts syndrome/SC phocomelia", "Roberts-SC phocomelia syndrome", "ROBERTS-SC PHOCOMELIA SYNDROME", "Roberts tetraphocomelia syndrome", "roberts tetraphocomelia syndrome", "Roberts pseudothalidomide syndrome", "Roberts' pseudothalidomide syndrome", "Phocomelia-Pseudothalidomide Syndrome", "Tetraphocomelia-Cleft Palate Syndrome", "tetraphocomelia-cleft palate syndrome", "Phocomelia-pseudothalidomide syndrome", "tetraphocomelia-cleft lip-palate syndrome", "Roberts-SC phocomelia syndrome (disorder)", "Roberts' pseudothalidomide syndrome (diagnosis)", "hypomelia-hypotrichosis-facial hemangioma syndrome", "Hypomelia-hypotrichosis-facial hemangioma syndrome", "Hypomelia Hypotrichosis Facial Hemangioma Syndrome", "Hypomelia hypotrichosis facial hemangioma syndrome", "Hypomelia hypotrichosis facial haemangioma syndrome", "Hypomelia-hypotrichosis-facial haemangioma syndrome", "LONG BONE DEFICIENCIES ASSOCIATED WITH CLEFT LIP-PALATE", "long bone deficiencies associated with cleft lip-palate", "Long bone deficiencies associated with cleft lip-palate", "SC phocomelia syndrome (mild variant of Roberts syndrome)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Roberts syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0005374", "names": ["Bone Marrow Tumor", "bone marrow tumor", "Bone marrow tumor", "bone Marrow tumor", "bone cancer marrow", "bone marrow cancer", "cancer bone marrow", "Bone marrow--Tumors", "bone marrow neoplasm", "Bone Marrow Neoplasm", "tumor of bone marrow", "bone marrow neoplasms", "Neoplasm, Bone Marrow", "Bone Marrow Neoplasms", "Neoplasms, Bone Marrow", "Neoplasm of bone marrow", "neoplasm of bone marrow", "Neoplasm of Bone Marrow", "malignant bone marrow tumor", "myeloproliferative disorder", "malignant bone Marrow tumor", "bone marrow neoplasm (disease)", "malignant neoplasm of bone marrow", "Neoplasm of bone marrow (disorder)", "Chronic Myeloproliferative Disease", "neoplasm of bone marrow (diagnosis)", "NCI CTEP SDC Chronic Myeloproliferative Disease Sub-Category Terminology", "NCI CTEP Simple Disease Classification Chronic Myeloproliferative Disease Sub-Category Terminology"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bone marrow neoplasm", "shortest_name_length": 17}
{"curie": "MONDO:0004440", "names": ["Pineal Meningioma", "Pineal meningioma", "pineal meningioma", "Pineal Area Meningioma", "pineal area meningioma", "pineal gland meningioma", "Pineal Gland Meningioma", "Pineal Region Meningioma", "pineal region meningioma", "meningioma of pineal area", "Meningioma of Pineal Area", "meningioma of pineal gland", "Meningioma of Pineal Gland", "Meningioma of Pineal Region", "meningioma of pineal region", "meningioma of the pineal area", "Meningioma of the Pineal Area", "meningioma of the pineal gland", "Meningioma of the Pineal Gland", "meningioma of the pineal region", "Meningioma of the Pineal Region", "pineal body meningioma (disease)", "meningioma (disease) of pineal body"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pineal region meningioma", "shortest_name_length": 17}
{"curie": "MONDO:0015574", "names": ["chronic cutaneous lupus erythematosus", "cutaneous lupus erythematosus, chronic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic cutaneous lupus erythematosus", "shortest_name_length": 37}
{"curie": "UMLS:C2242684", "names": ["Gastroenteritis sapovirus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastroenteritis sapovirus", "shortest_name_length": 25}
{"curie": "MONDO:0007023", "names": ["yersinia", "YERSINOSIS", "yersinosis", "YERSINIOSES", "Yersinioses", "yersiniosis", "Yersiniosis", "yersinioses", "Yersiniosis, NOS", "yersinia infection", "Yersinia Infection", "Yersinia infection", "Infection, Yersinia", "Yersinia Infections", "Yersinia infections", "infection, Yersinia", "infections, Yersinia", "Infections, Yersinia", "Yersiniosis (disorder)", "Yersinia infection NOS", "yersiniosis (diagnosis)", "Yersinia infectious disease", "Yersinia <bacteria> infection", "infections, Yersinia <bacteria>"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Yersinia infectious disease", "shortest_name_length": 8}
{"curie": "MONDO:0010308", "names": ["XLTDA", "X-linked thrombocytopenia, with or without dyserythropoietic Anemia", "X-linked Thrombocytopenia, with or without Dyserythropoietic Anemia", "THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA", "thrombocytopenia, X-linked, with or without dyserythropoietic anemia", "thrombocytopenia, X-linked, with or without dyserythropoietic anemia, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombocytopenia, X-linked, with or without dyserythropoietic anemia", "shortest_name_length": 5}
{"curie": "UMLS:C5239091", "names": ["SAMD9L-Associated Familial MDS", "SAMD9L-Associated Familial Myelodysplastic Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SAMD9L-Associated Familial Myelodysplastic Syndrome", "shortest_name_length": 30}
{"curie": "MONDO:0018670", "names": ["symptomatic form of fragile X syndrome in female carrier"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "symptomatic form of fragile X syndrome in female carrier", "shortest_name_length": 56}
{"curie": "UMLS:C1519919", "names": ["Vaginal Deep Angiomyxoma", "Vaginal Aggressive Angiomyxoma", "Vaginal Deep \"Aggressive\" Angiomyxoma", "Vaginal Deep (Aggressive) Angiomyxoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Deep (Aggressive) Angiomyxoma", "shortest_name_length": 24}
{"curie": "UMLS:C2747792", "names": ["Fingerprint loss"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fingerprint loss", "shortest_name_length": 16}
{"curie": "MONDO:0009260", "names": ["GM1G1", "Glb1 deficiency", "GLB deficiency type 1", "Norman-Landing disease", "Type I GM1-Gangliosidosis", "GM1 gangliosidosis type 1", "GM1 gangliosidosis type I", "Type I GM1-Gangliosidoses", "GM1-Gangliosidosis, Type I", "GM1-gangliosidosis, type 1", "GM1 Gangliosidosis, Type I", "GM1-Gangliosidoses, Type I", "Generalized Gangliosidosis", "Generalized gangliosidosis", "GM1 gangliosidosis, type I", "GM1-gangliosidosis, type I", "Generalised gangliosidosis", "GM1 gangliosidosis, type 1", "GM1-GANGLIOSIDOSIS, TYPE I", "Gangliosidosis GM1, Type 1", "Infantile Gangliosidosis GM1", "infantile GM1 gangliosidosis", "GM>1< gangliosidosis, type 1", "Infantile GM1 gangliosidosis", "Gangliosidosis GM1, Infantile", "Infantile GM>1< gangliosidosis", "Beta-galactosidase-1 deficiency", "Beta galactosidase deficiency type 1", "GM1 gangliosidosis type I (diagnosis)", "gangliosidosis generalized GM1 type 1", "GM<sub>1</sub> gangliosidosis, type 1", "Gangliosidosis Generalized GM1, Type 1", "Infantile GM<sub>1</sub> gangliosidosis", "GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I", "Gangliosidosis, Generalized GM1, Type I", "gangliosidosis, generalized GM1, type 1", "Infantile GM1 gangliosidosis (disorder)", "Gangliosidosis, Generalized GM1, Type 1", "GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 1", "gangliosidosis generalized GM1 infantile form", "Infantile gangliosidosis with bony involvement", "Gangliosidosis, Generalized GM1, Infantile Form", "GANGLIOSIDOSIS, GENERALIZED GM1, INFANTILE FORM", "gangliosidosis, generalized GM1, infantile form", "Gangliosidosis, Generalized GM1, Type 1 (disorder)", "GM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT", "Gm1 Gangliosidosis, Type I, with Cardiac Involvement", "GM1-gangliosidosis, type I, with Cardiac involvement", "Deficiency of beta-galactosidase isoenzymes A, B and C", "Deficiency of beta-galactosidase isoenzymes A, B AND C", "GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I, WITH CARDIAC INVOLVEMENT", "gangliosidosis, generalized GM1, type I, with Cardiac involvement", "Gangliosidosis, Generalized GM1, Type I, with Cardiac Involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "GM1 gangliosidosis type 1", "shortest_name_length": 5}
{"curie": "MONDO:0030921", "names": ["MRD55", "autosomal dominant mental retardation 55", "autosomal dominant intellectual disability 55", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 55, WITH SEIZURES", "mental retardation, autosomal dominant 55, with seizures", "autosomal dominant intellectual developmental disorder 55", "intellectual disability, autosomal dominant 55, with seizures", "autosomal dominant intellectual developmental disorder-55 with seizures", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 55, WITH SEIZURES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 55, with seizures", "shortest_name_length": 5}
{"curie": "MONDO:0022518", "names": ["AIED", "autoimmune inner ear disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune inner ear disease", "shortest_name_length": 4}
{"curie": "UMLS:C4521793", "names": ["IV", "Stage IV Gastric (Stomach) Cancer", "Pathologic Stage IV Gastric Cancer AJCC v8", "Pathologic Stage IV Gastric Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IV Gastric Cancer AJCC v8", "shortest_name_length": 2}
{"curie": "UMLS:C5237455", "names": ["Advanced Leiomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Leiomyosarcoma", "shortest_name_length": 23}
{"curie": "MONDO:0015725", "names": ["mosaic trisomy 14", "Trisomy 14 mosaic", "trisomy mosaic 14", "Mosaic trisomy 14", "Trisomy 14 Mosaicism", "Trisomy 14 mosaicism", "trisomy 14 mosaicism", "Mosaic trisomy type 14", "Mosaic trisomy 14 syndrome", "Mosaic trisomy chromosome 14", "Chromosome 14, trisomy mosaic", "14 trisomy mosaicism syndrome", "Trisomy 14 mosaicism syndrome", "Mosaic trisomy 14 syndrome (disorder)", "Mosaic trisomy 14 syndrome (diagnosis)", "anomaly of chromosome pair mosaic trisomy 14 syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mosaic trisomy 14", "shortest_name_length": 17}
{"curie": "UMLS:C1710419", "names": ["Thyroid Gland Hot Adenoma", "Thyroid Gland Toxic Adenoma", "Thyroid Gland Hyperfunctioning Adenoma", "Thyroid Gland Toxic (Hyperfunctioning) Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Hyperfunctioning Adenoma", "shortest_name_length": 25}
{"curie": "MONDO:0013152", "names": ["SLEB14", "SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 14", "systemic lupus erythematosus, susceptibility to, 14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "systemic lupus erythematosus, susceptibility to, 14", "shortest_name_length": 6}
{"curie": "MONDO:0044144", "names": ["panic disorder agoraphobia", "agoraphobia disorder panic", "Panic disorder with agoraphobia", "agoraphobia with panic disorder", "Panic Disorder with Agoraphobia", "panic disorder with agoraphobia", "Agoraphobia with panic disorder", "disorder; panic, with agoraphobia", "panic; disorder, with agoraphobia", "Panic disorder with agoraphobia, NOS", "Panic disorder with agoraphobia (disorder)", "panic disorder with agoraphobia (diagnosis)", "panic disorder with agoraphobia and panic attacks", "panic disorder with agoraphobia and panic attacks (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "panic disorder with agoraphobia", "shortest_name_length": 26}
{"curie": "MONDO:0018611", "names": ["early-onset lamellar cataract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early-onset lamellar cataract", "shortest_name_length": 29}
{"curie": "UMLS:C0854793", "names": ["Malignant liver tumor non-resectable", "Unresectable Malignant Liver Neoplasm", "Malignant liver tumour non-resectable", "Non-Resectable Malignant Liver Neoplasm", "Non-Resectable Hepatic Malignant Neoplasm", "Malignant hepatic neoplasm non-resectable", "Hepatic neoplasm malignant non-resectable", "Non-Resectable Malignant Neoplasm of Liver"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Resectable Malignant Liver Neoplasm", "shortest_name_length": 36}
{"curie": "MONDO:0023597", "names": ["Laryngeal papilloma", "Warts in the throat", "Laryngeal papillomas", "Laryngeal papillomatosis", "laryngeal papillomatosis", "Laryngeal Papillomatosis", "juvenile laryngeal papillomatosis", "Juvenile laryngeal papillomatosis", "recurrent laryngeal papillomatosis", "Recurrent laryngeal papillomatosis", "Laryngeal papillomatosis (disorder)", "Laryngeal papillomatosis (diagnosis)", "juvenile laryngeal papillomatosis (subtype)", "recurrent laryngeal papillomatosis (subtype)", "Recurrent Respiratory Papillomatosis of the Larynx", "benign neoplasm respiratory system recurrent papillomatosis laryngeal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laryngeal papillomatosis", "shortest_name_length": 19}
{"curie": "MONDO:0032827", "names": ["EIG16", "EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 16", "epilepsy, idiopathic generalized, susceptibility to, 16"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, idiopathic generalized, susceptibility to, 16", "shortest_name_length": 5}
{"curie": "UMLS:C1336148", "names": ["Stage IC Endometrial Cancer AJCC v6", "Stage IC Uterine Corpus Cancer AJCC v6", "Stage IC Uterine (including Endometrial) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IC Uterine Corpus Cancer AJCC v6", "shortest_name_length": 35}
{"curie": "MONDO:0004454", "names": ["Infantile Renal Fibrosarcoma", "Cellular Mesoblastic Nephroma", "Mesoblastic nephroma, cellular", "Cellular Congenital Mesoblastic Nephroma", "cellular congenital mesoblastic nephroma", "Mesoblastic nephroma, cellular (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cellular congenital mesoblastic nephroma", "shortest_name_length": 28}
{"curie": "MONDO:0008377", "names": ["RP", "RP1", "retinitis pigmentosa", "Retinitis pigmentosa 1", "RETINITIS PIGMENTOSA 1", "retinitis pigmentosa 1", "RP1 retinitis pigmentosa", "retinitis pigmentosa type 1", "retinitis pigmentosa caused by mutation in RP1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 1", "shortest_name_length": 2}
{"curie": "UMLS:C1112498", "names": ["Parathyroid gland abscess", "Parathyroid Gland Abscess"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parathyroid gland abscess", "shortest_name_length": 25}
{"curie": "UMLS:C0677501", "names": ["Renal diabetes insipidus", "ADH-resistant diabetes insipidus", "Vasopressin-resistant hyposthenuria", "Adiuretin-resistant diabetes insipidus", "Primary nephrogenic diabetes insipidus", "Familial nephrogenic diabetes insipidus", "vasopressin resistant diabetes insipidus", "Vasopressin-resistant diabetes insipidus", "Hereditary nephrogenic diabetes insipidus", "Congenital Nephrogenic Diabetes Insipidus", "nephrogenic diabetes insipidus congenital", "Congenital nephrogenic diabetes insipidus", "DIABETES INSIPIDUS, VASOPRESSIN-RESISTANT", "congenital nephrogenic diabetes insipidus", "vasopressin; resistant diabetes insipidus", "Vasopressin-unresponsiveness hyposthenuria", "diabetes; insipidus, vasopressin resistant", "Hereditary nephrogenic diabetes insipidus, NOS", "Hereditary nephrogenic diabetes insipidus (disorder)", "Nephrogenic/vasopressin-resistant diabetes insipidus", "congenital nephrogenic diabetes insipidus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Nephrogenic Diabetes Insipidus", "shortest_name_length": 24}
{"curie": "MONDO:0001413", "names": ["Ulceroglandular tularemia", "ulceroglandular tularemia", "ulceroglandular; tularemia", "tularemia; ulceroglandular", "Ulceroglandular tularaemia", "Ulceroglandular tularemia (disorder)", "ulceroglandular tularemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ulceroglandular tularemia", "shortest_name_length": 25}
{"curie": "MONDO:0020389", "names": ["APV/PDA, non-Fallot type", "PVA/PDA, non-Fallot type", "pulmonary valve agenesis-ventricular septal defect-persistent ductus arteriosus syndrome", "pulmonary valve agenesis-intact ventricular septum-persistent ductus arteriosus syndrome", "absence of pulmonary valve-ventricular septal defect-persistent ductus arteriosus syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary valve agenesis-ventricular septal defect-persistent ductus arteriosus syndrome", "shortest_name_length": 24}
{"curie": "UMLS:C3273099", "names": ["Gallbladder MCN with Intermediate Grade Intraepithelial Neoplasia", "Gallbladder Mucinous Cystic Neoplasm with Intermediate Grade Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gallbladder Mucinous Cystic Neoplasm with Intermediate Grade Intraepithelial Neoplasia", "shortest_name_length": 65}
{"curie": "MONDO:0019538", "names": ["Gaisböck", "GaisböCK syndrome", "GAISBOECK DISEASE", "Gaisbock syndrome", "gaisbock syndrome", "GAISBOCK SYNDROME", "Gaisböck syndrome", "gaisbocks syndrome", "Pseudopolycythemia", "polycythemia stress", "stress polycythemia", "Stress polycythemia", "Gaisbock's syndrome", "Pseudopolycythaemia", "gaisbock's syndrome", "Stress Polycythemia", "stress; polycythemia", "POLYCYTHEMIA, STRESS", "Polycythemia, stress", "polycythemia; stress", "Stress polycythaemia", "Gaisboeck's syndrome", "Stress erythrocytosis", "stress erythrocytosis", "emotional polycythemia", "ERYTHROCYTOSIS, STRESS", "Emotional polycythemia", "POLYCYTHEMIA, EMOTIONAL", "polycythemia, emotional", "emotional; polycythemia", "polycythemia; emotional", "Emotional polycythaemia", "Polycythemia, emotional", "polycythemia hypertonica", "Polycythemia hypertonica", "polycythemia; hypertonica", "Polycythaemia hypertonica", "hypertonica; polycythemia", "polycythaemia hypertonica", "Stress polycythemia (disorder)", "Gaisbock's syndrome (disorder)", "stress polycythemia (diagnosis)", "secondary polycythemia emotional", "emotional polycythemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gaisbock syndrome", "shortest_name_length": 8}
{"curie": "UMLS:C4727772", "names": ["Locally Advanced Soft Tissue Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Soft Tissue Sarcoma", "shortest_name_length": 36}
{"curie": "UMLS:C5671071", "names": ["SUPERNUMERARY HEMIVERTEBRA", "Supernumerary Hemivertebra"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Supernumerary Hemivertebra", "shortest_name_length": 26}
{"curie": "MONDO:0014805", "names": ["HAFOUS", "Del(16)(p13.2)", "monosomy 16p13.2", "Hao-Fountain syndrome", "HAO-FOUNTAIN SYNDROME", "16p13.2 microdeletion syndrome", "CHROMOSOME 16p13.2 DELETION SYNDROME", "chromosome 16p13.2 deletion syndrome", "chromosome 16P13.2 deletion syndrome", "USP7-related neurodevelopmental disorder", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH IMPAIRED SPEECH, BEHAVIORAL ABNORMALITIES, AND DYSMORPHIC FACIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hao-Fountain syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C1332040", "names": ["AIDS Related Cervical Cancer", "AIDS-related cervical cancer", "AIDS-Related Cervical Cancer", "AIDS-Related Cervix Carcinoma", "AIDS-Related Cervical Carcinoma", "AIDS-Related Uterine Cervix Cancer", "AIDS-Related Cancer of Uterine Cervix", "AIDS-Related Uterine Cervix Carcinoma", "AIDS Related Carcinoma of Uterine Cervix", "AIDS-Related Cancer of the Uterine Cervix", "AIDS Related Carcinoma of the Uterine Cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Cervical Carcinoma", "shortest_name_length": 28}
{"curie": "UMLS:C4289813", "names": ["Cervical Mesonephric Remnants and Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Mesonephric Remnants and Hyperplasia", "shortest_name_length": 45}
{"curie": "MONDO:0008610", "names": ["CBT", "tritanopia", "Tritanopia", "TRITANOPIA", "Tritanomaly", "tritanomaly", "tritan defect", "Tritan Defect", "Tritan defect", "blue color defect", "blue colorblindness", "BLUE COLORBLINDNESS", "BLUE COLOR BLINDNESS", "blue color blindness", "Tritan defect (blue)", "Blue Color Blindness", "Tritanopia (disorder)", "congenital tritanopia", "blue colour blindness", "Blue colour blindness", "Congenital tritanopia", "Color Blindness, Blue", "colorblindness, tritan", "COLORBLINDNESS, TRITAN", "Tritan colour blindness", "tritan colour blindness", "Tritan defect (disorder)", "tritan defect (diagnosis)", "COLORBLINDNESS, TRITANOPIC", "colorblindness, tritanopic", "Blue yellow color blindness", "Blue-yellow dyschromatopsia", "Blue-yellow color blindness", "Dyschromatopsia, blue-yellow", "Blue yellow colour blindness", "Blue/yellow color vision defect", "Blue/yellow colour vision defect", "blue color defect (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blue color blindness", "shortest_name_length": 3}
{"curie": "MONDO:0018544", "names": ["ald", "ALD", "X ALD", "X-ALD", "X-linked ALD", "Schilder Disease", "ABCD1 deficiency", "diffuse sclerosis", "adrenoleucodystrophy", "Adrenoleucodystrophy", "Adrenoleukodystrophy", "adrenoleukodystrophy", "ADRENOLEUKODYSTROPHY", "adrenomyeloneuropathy", "Bronze Schilder disease", "Fanconi-Prader syndrome", "Bronze Schilder Disease", "bronze Schilder disease", "Bronze-Schilder disease", "BRONZE SCHILDER DISEASE", "Schilder-Addison complex", "Schilder Addison Complex", "Addison-Schilder disease", "Schilder-Addison Complex", "Schilder-Addison; complex", "complex; Schilder-Addison", "complex; Addison-Schilder", "Addison-Schilder; complex", "Addison-Schilder syndrome", "adrenoleukomyeloneuropathy", "ALD - adrenoleukodystrophy", "ALD (Adrenoleukodystrophy)", "adrenoleukodystrophy (ALD)", "melanodermic leukodystrophy", "Melanodermic Leukodystrophy", "MELANODERMIC LEUKODYSTROPHY", "adrenomyeloneuropathy, adult", "Leukodystrophy, Melanodermic", "X Linked Adrenoleukodystrophy", "X-Linked Adrenoleukodystrophy", "X-linked adrenoleukodystrophy", "X-linked adrenoleucodystrophy", "Adrenoleukodystrophy, X-Linked", "Siemerling-Creutzfeldt disease", "Siemerling Creutzfeldt Disease", "Siemerling-Creutzfeldt Disease", "adrenoleukodystrophy, X-linked", "SIEMERLING-CREUTZFELDT DISEASE", "Leukodystrophies, Melanodermic", "Adrenoleukodystrophy (disorder)", "Siemerling-Creutzfeldt syndrome", "sudanophilic cerebral sclerosis", "adrenoleukomyeloneuropathy (ALMN)", "Encephalitis periaxialis, Schilder's", "Encephalitis periaxialis concentrica", "encephalitis periaxialis, Schilder's", "encephalitis periaxialis concentrica", "X ALD (X Linked Adrenoleukodystrophy)", "X-ALD (X-Linked Adrenoleukodystrophy)", "ADDISON DISEASE AND CEREBRAL SCLEROSIS", "diffuse cerebral sclerosis of Schilder", "Addison Disease and Cerebral Sclerosis", "Sex-linked metachromatic leukodystrophy", "adrenoleukodystrophy, X-linked recessive", "X-linked adrenoleukodystrophy (diagnosis)", "Addison disease-cerebral sclerosis syndrome", "Addison disease-spastic paraplegia syndrome", "X-linked adrenoleukodystrophy, unspecified type", "adrenomyeloneuropathy, adult, X-linked recessive", "adrenocortical atrophy-cerebral sclerosis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adrenoleukodystrophy", "shortest_name_length": 3}
{"curie": "MONDO:0022575", "names": ["biliary hypoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "biliary hypoplasia", "shortest_name_length": 18}
{"curie": "MONDO:0025066", "names": ["Greasy pig disease", "Greasy Pig Disease", "greasy pig disease", "Disease, Greasy Pig", "disease, greasy pig", "Seborrhea oleosa suis", "Seborrhoea oleosa suis", "Impetigo contagiosa suis", "Swine Exudative Dermatitis", "swine exudative dermatitis", "Contagious porcine pyoderma", "swine exudative Dermatitides", "Swine Exudative Dermatitides", "Exudative Dermatitis of Swine", "exudative dermatitis of swine", "Exudative epidermitis of swine", "Epidermitis, exudative of swine", "Epidermitis, Exudative of Swine", "epidermitis, exudative, of swine", "Epidermitis, Exudative, of Swine", "Contagious porcine pyoderma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermitis, exudative, of swine", "shortest_name_length": 18}
{"curie": "MONDO:0023140", "names": ["fenton Wilkinson Toselano syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fenton Wilkinson Toselano syndrome", "shortest_name_length": 34}
{"curie": "UMLS:C4225591", "names": ["MITOCHONDRIAL MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MITOCHONDRIAL MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 3", "shortest_name_length": 67}
{"curie": "MONDO:0007923", "names": ["COLE-HUGHES SYNDROME", "Cole-Hughes syndrome", "Benign familial macrocephaly", "benign familial macrocephaly", "Macrocephaly, benign familial", "MACROCEPHALY, BENIGN FAMILIAL", "macrocephaly, benign familial", "benign familial megalencephaly", "Benign familial megalencephaly", "benign familial macrocephaly (BFM)", "autosomal dominant macrocephaly syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macrocephaly, benign familial", "shortest_name_length": 20}
{"curie": "MONDO:0800128", "names": ["combined immunodeficiency due to POLE2 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined immunodeficiency due to POLE2 deficiency", "shortest_name_length": 49}
{"curie": "MONDO:0001360", "names": ["Blind hypotensive eye", "BLIND HYPOTENSIVE EYE", "blind hypotensive eye", "blind hypotensive eye (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blind hypotensive eye", "shortest_name_length": 21}
{"curie": "MONDO:0004267", "names": ["squamous papillomatosis", "Squamous papillomatosis", "Squamous Papillomatosis", "Papillomatosis, squamous", "Squamous papillomatosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "squamous papillomatosis", "shortest_name_length": 23}
{"curie": "UMLS:C4727182", "names": ["Recurrent Cushing Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Cushing Disease", "shortest_name_length": 25}
{"curie": "MONDO:0016491", "names": ["BETA-E-THALASSEMIA", "E-beta-thalassemia", "Hemoglobin E-beta thalassemia", "HbE-beta-thalassemia syndrome", "hemoglobin E-beta thalassemia", "Hemoglobin E/beta thalassemia disease", "Hemoglobin E-beta-thalassemia syndrome", "hemoglobin E-beta-thalassemia syndrome", "Haemoglobin E/beta thalassaemia disease", "hemoglobin E-beta thalassemia (diagnosis)", "Hemoglobin E/beta thalassemia disease (disorder)", "Double heterozygous for Hb E and beta thalassemia", "Double heterozygous for Hb E and beta thalassaemia", "disease (or disorder); hemoglobin or Hb, E (Hb-E), thalassemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemoglobin E-beta-thalassemia syndrome", "shortest_name_length": 18}
{"curie": "MONDO:0012824", "names": ["HLD4", "Mitchap60 disease", "MITCHAP60 DISEASE", "MitCHAP60 disease", "HSPD1 leukodystrophy", "hypomyelinating leukodystrophy 4", "mitochondrial HSP60 chaperonopathy", "Mitochondrial Hsp60 Chaperonopathy", "MITOCHONDRIAL HSP60 CHAPERONOPATHY", "Leukodystrophy, Hypomyelinating, 4", "leukodystrophy, hypomyelinating, 4", "mitochondrial Hsp60 chaperonopathy", "LEUKODYSTROPHY, HYPOMYELINATING, 4", "Mitochondrial HSP60 chaperonopathy", "hypomyelinating leukodystrophy type 4", "leukodystrophy, hypomyelinating, type 4", "leukodystrophy caused by mutation in HSPD1", "Pelizaeus Merzbacher like disease due to HSPD1 mutation", "Pelizaeus-Merzbacher-like disease due to HSPD1 mutation", "Pelizaeus Merzbacher like disease due to HSPD1 mutation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypomyelinating leukodystrophy 4", "shortest_name_length": 4}
{"curie": "UMLS:C1334991", "names": ["Localized Neoplasm", "Non-metastatic Disease", "Non-Metastatic Neoplasm", "tumor confined to organ of origin", "tumor_confined_to_organ_of_origin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized Neoplasm", "shortest_name_length": 18}
{"curie": "UMLS:C3890205", "names": ["Polyarticular JIA, RF-", "Juvenile seronegative polyarthritis", "Juvenile polyarthritis (seronegative)", "Rheumatoid factor-negative polyarticular JIA", "Juvenile seronegative polyarthritis (disorder)", "Polyarticular Juvenile Idiopathic Arthritis, RF-", "Juvenile polyarthritis without rheumatoid factor", "Juvenile rheumatoid factor-negative polyarthritis", "Juvenile chronic arthritis, polyarticular seronegative", "polyarticular juvenile idiopathic arthritis RF negative", "Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis", "Polyarticular Juvenile Idiopathic Arthritis, Rheumatoid Factor Negative", "Juvenile idiopathic arthritis, polyarthritis, rheumatoid factor negative", "polyarticular juvenile idiopathic arthritis with negative rheumatoid factor", "polyarticular juvenile idiopathic arthritis with negative rheumatoid factor (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Polyarticular Juvenile Idiopathic Arthritis, Rheumatoid Factor Negative", "shortest_name_length": 22}
{"curie": "MONDO:0014884", "names": ["PFIC5", "NR1H4 deficiency", "progressive familial intrahepatic cholestasis 5", "cholestasis, progressive familial intrahepatic, 5", "CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 5", "NR1H4 progressive familial intrahepatic cholestasis", "Progressive familial intrahepatic cholestasis type 5", "cholestasis, progressive familial intrahepatic, type 5", "cholestasis, progressive familial intrahepatic, 5; PFIC5", "progressive familial intrahepatic cholestasis caused by mutation in NR1H4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholestasis, progressive familial intrahepatic, 5", "shortest_name_length": 5}
{"curie": "UMLS:C3714670", "names": ["Aircraft Accident", "Aircraft accident NOS", "Airplane accident, NOS", "Aircraft accident, NOS", "ACCIDENTS INVOLVING AIRCRAFT", "Accident involving aircraft, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Accident involving aircraft, NOS", "shortest_name_length": 17}
{"curie": "MONDO:0006799", "names": ["Hypothalamus Tumor", "Hypothalamic Tumor", "tumor hypothalamus", "hypothalamic tumor", "Hypothalamic tumor", "hypothalamus tumor", "Hypothalamus Tumors", "hypothalamus tumour", "hypothalamic tumors", "Tumor, Hypothalamic", "Tumor, Hypothalamus", "Hypothalamic Tumors", "hypothalamus tumors", "Tumors, Hypothalamus", "Tumors, Hypothalamic", "tumor of hypothalamus", "hypothalamus neoplasm", "Tumor of hypothalamus", "Hypothalamic Neoplasm", "Tumor of Hypothalamus", "Hypothalamus Neoplasm", "hypothalamic neoplasm", "Tumour of hypothalamus", "Neoplasm, Hypothalamus", "hypothalamic neoplasms", "Hypothalamus Neoplasms", "Hypothalamic Neoplasms", "Neoplasm, Hypothalamic", "Neoplasms, Hypothalamic", "Neoplasms, Hypothalamus", "neoplasm of hypothalamus", "Neoplasm of Hypothalamus", "tumor of the hypothalamus", "Tumor of the Hypothalamus", "neoplasm of the Hypothalamus", "Neoplasm of the Hypothalamus", "neoplasm of the hypothalamus", "Tumor of hypothalamus (disorder)", "neoplasm of hypothalamus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypothalamic neoplasm", "shortest_name_length": 18}
{"curie": "UMLS:C4520990", "names": ["Stage 0 Nasopharynx Lymphoepithelioma", "Stage 0 Nasopharyngeal Lymphoepithelioma", "Stage 0 Lymphoepithelioma of Nasopharynx", "Stage 0 Lymphoepithelioma of the Nasopharynx", "Nasopharyngeal Undifferentiated Carcinoma Stage O", "Stage 0 Nasopharyngeal Undifferentiated Carcinoma", "Stage 0 Undifferentiated Nasopharyngeal Throat Cancer", "Stage 0 Nasopharyngeal Undifferentiated Carcinoma AJCC v7", "Stage 0 Nasopharyngeal Undifferentiated Carcinoma AJCC v8", "Stage 0 Nasopharyngeal Undifferentiated Carcinoma AJCC v6", "Stage 0 Nasopharyngeal Undifferentiated Carcinoma AJCC v6, v7, and v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Nasopharyngeal Undifferentiated Carcinoma AJCC v6, v7, and v8", "shortest_name_length": 37}
{"curie": "OMIM:110900", "names": [], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"]}
{"curie": "UMLS:C1332275", "names": ["Anal Premalignant Condition", "Anal Precancerous Condition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anal Precancerous Condition", "shortest_name_length": 27}
{"curie": "UMLS:C0037316", "names": ["Sleep deficit", "sleep deprivation", "Sleep deprivation", "Sleep Deprivation", "sleep deprivations", "Deprivation, Sleep", "not enough sleeping", "RNDx sleep deprivation", "Lack of adequate sleep", "Sleep deprivation (finding)", "RNDx sleep deprivation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sleep Deprivation", "shortest_name_length": 13}
{"curie": "UMLS:C1336419", "names": ["stage IV hypopharynx cancer", "Stage IV Hypopharyngeal Throat Cancer", "Stage IV Hypopharynx Carcinoma AJCC v6", "Stage IV Hypopharyngeal Carcinoma AJCC v6", "Stage IV Carcinoma of Hypopharynx AJCC v6", "Stage IV Carcinoma of the Hypopharynx AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Hypopharyngeal Carcinoma AJCC v6", "shortest_name_length": 27}
{"curie": "UMLS:C5419801", "names": ["Colorectal Neuroendocrine Tumor G3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Neuroendocrine Tumor G3", "shortest_name_length": 34}
{"curie": "UMLS:C0027666", "names": ["Tumors, Radiation-induced", "Radiation Induced Neoplasm", "radiation related neoplasm", "Radiation-Induced Neoplasm", "Radiation-Related Neoplasm", "Radiation-Induced Neoplasms", "Radiation Induced Neoplasms", "Neoplasm, Radiation-Induced", "Neoplasms, Radiation-Induced", "Neoplasms, Radiation Induced"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplasms, Radiation-Induced", "shortest_name_length": 25}
{"curie": "UMLS:C5418773", "names": ["Recurrent Primary Peritoneal Undifferentiated Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Primary Peritoneal Undifferentiated Carcinoma", "shortest_name_length": 55}
{"curie": "UMLS:C1706810", "names": ["Androgen-Producing Adrenal Gland Adenoma", "Androgen Producing Adrenal Cortex Adenoma", "Androgen-Producing Adrenal Cortex Adenoma", "Androgen Producing Adrenal Cortical Adenoma", "Androgen-Producing Adrenal Cortical Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Androgen-Producing Adrenal Cortical Adenoma", "shortest_name_length": 40}
{"curie": "UMLS:C1879790", "names": ["Skin Basal Cell Carcinoma with Adnexal Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin Basal Cell Carcinoma with Adnexal Differentiation", "shortest_name_length": 54}
{"curie": "UMLS:C1335707", "names": ["Recurrent Malignant Endocervical Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Malignant Endocervical Neoplasm", "shortest_name_length": 41}
{"curie": "MONDO:0013036", "names": ["Zechi-Ceide syndrome", "ZECHI-CEIDE SYNDROME", "Zechi-Ceide Syndrome", "Zechi Ceide syndrome", "Zechi Ceide syndrome (disorder)", "Zechi Ceide syndrome (diagnosis)", "multiple malformation syndrome Zechi Ceide syndrome", "occipital atretic cephalocele, unusual facies and large feet", "OCCIPITAL ATRETIC CEPHALOCELE, UNUSUAL FACIES, AND LARGE FEET", "occipital atretic cephalocele, unusual facies, and large feet", "Occipital Atretic Cephalocele, Unusual Facies, and Large Feet", "Occipital atretic cephalocele-unusual facies-large feet syndrome", "occipital atretic cephalocele-unusual facies-large feet syndrome", "Occipital atretic cephalocele, unusual facies, large feet syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Zechi-Ceide syndrome", "shortest_name_length": 20}
{"curie": "MONDO:0019445", "names": ["Trichofolliculoma", "trichofolliculoma", "Recurrent trichofolliculoma", "Trichofolliculoma (disorder)", "Trichofolliculoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichofolliculoma", "shortest_name_length": 17}
{"curie": "UMLS:C0235972", "names": ["retinal deposits", "Retinal deposits", "RETINAL DEPOSITS", "Retinal deposits (disorder)", "retinal deposits (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retinal deposits", "shortest_name_length": 16}
{"curie": "MONDO:0006477", "names": ["anaplastic ovarian carcinoma", "Anaplastic Ovarian Carcinoma", "Anaplastic Carcinoma of Ovary", "anaplastic carcinoma of ovary", "Undifferentiated Ovarian Cancer", "undifferentiated ovarian cancer", "Undifferentiated ovarian cancer", "ovary undifferentiated carcinoma", "Anaplastic Carcinoma of the Ovary", "anaplastic carcinoma of the ovary", "ovarian undifferentiated carcinoma", "Undifferentiated Ovarian Carcinoma", "undifferentiated ovarian carcinoma", "Ovarian Undifferentiated Carcinoma", "Undifferentiated carcinoma of ovary", "Undifferentiated Carcinoma of Ovary", "undifferentiated carcinoma of ovary", "Undifferentiated Carcinoma of the Ovary", "undifferentiated carcinoma of the ovary", "anaplastic carcinoma of ovary (diagnosis)", "Undifferentiated carcinoma of ovary (disorder)", "undifferentiated carcinoma of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "undifferentiated ovarian carcinoma", "shortest_name_length": 28}
{"curie": "UMLS:C0042021", "names": ["urinary fistula", "Urinary Fistula", "Urinary fistula", "Urinary Fistulas", "Fistula, Urinary", "urinary fistulas", "fistula; urinary", "urinary; fistula", "Fistulas, Urinary", "Urological fistula", "Urinary fistula NOS", "Urinary fistula, NOS", "Urinary Tract Fistula", "Urinary fistula (disorder)", "urinary fistula (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urinary Tract Fistula", "shortest_name_length": 15}
{"curie": "UMLS:C0342317", "names": ["Hypoglycemia unawareness", "Hypoglycaemia unawareness", "Loss of hypoglycemic warning", "Loss of hypoglycaemic warning", "Loss of hypoglycemic warning due to diabetes mellitus", "Loss of hypoglycaemic warning due to diabetes mellitus", "Loss of hypoglycemic warning due to diabetes mellitus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Loss of hypoglycemic warning due to diabetes mellitus", "shortest_name_length": 24}
{"curie": "MONDO:0001931", "names": ["PERICHOLANGITIS", "Pericholangitis", "pericholangitis", "Pericholangitis, NOS", "Pericholangitis (disorder)", "pericholangitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pericholangitis", "shortest_name_length": 15}
{"curie": "MONDO:0016869", "names": ["partial deletion of chromosome 4", "partial monosomy of chromosome 4", "partial deletion of chromosome type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of chromosome 4", "shortest_name_length": 32}
{"curie": "UMLS:C3272810", "names": ["Colon Serrated Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colon Serrated Adenocarcinoma", "shortest_name_length": 29}
{"curie": "UMLS:C0423086", "names": ["stare", "stared", "stares", "staring", "Staring", "Gazing fixedly", "Staring (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Staring", "shortest_name_length": 5}
{"curie": "UMLS:C4054045", "names": ["Secondary Collapsing Glomerulopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary Collapsing Glomerulopathy", "shortest_name_length": 35}
{"curie": "UMLS:C4763837", "names": ["Metastatic Bladder Small Cell Carcinoma", "Metastatic Bladder Small Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Bladder Small Cell Neuroendocrine Carcinoma", "shortest_name_length": 39}
{"curie": "UMLS:C1707296", "names": ["Heart Cavernous Hemangioma", "Cardiac Cavernous Hemangioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiac Cavernous Hemangioma", "shortest_name_length": 26}
{"curie": "MONDO:0012671", "names": ["ETM3", "essential tremor 3", "hereditary essential tremor 3", "tremor, hereditary essential, 3", "TREMOR, HEREDITARY ESSENTIAL, 3", "essential tremor, hereditary, 3", "Tremor, Hereditary Essential, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tremor, hereditary essential, 3", "shortest_name_length": 4}
{"curie": "UMLS:C3665333", "names": ["KID syndrome", "KID/HID syndrome", "Ichthyosis hystrix Rheydt type", "Keratitis, Ichthyosis, and Deafness", "Keratitis-Ichthyosis-Deafness Syndrome", "Keratitis-ichthyosis-deafness syndrome", "Keratitis ichthyosis deafness syndrome", "Keratitis ichthyosis and deafness syndrome", "KIDS - Keratitis ichthyosis and deafness syndrome", "Keratitis ichthyosis and deafness syndrome (disorder)", "Keratitis, ichthyosis, deafness/hystrix-like ichthyosis deafness syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Keratitis-Ichthyosis-Deafness Syndrome", "shortest_name_length": 12}
{"curie": "UMLS:C4055125", "names": ["Disrupted Suture", "Stitches Coming Loose"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disrupted Suture", "shortest_name_length": 16}
{"curie": "MONDO:0004016", "names": ["pineal area mature teratoma", "Pineal Area Mature Teratoma", "pineal region mature teratoma", "Pineal Region Mature Teratoma", "mature teratoma of pineal area", "Mature Teratoma of Pineal Area", "Mature Teratoma of Pineal Region", "mature teratoma of pineal region", "Mature teratoma of the Pineal Area", "mature teratoma of the pineal area", "Mature Teratoma of the Pineal Area", "mature teratoma of the pineal region", "Mature Teratoma of the Pineal Region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pineal region mature teratoma", "shortest_name_length": 27}
{"curie": "MONDO:0012037", "names": ["MRT3", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 3", "Mental Retardation, Autosomal Recessive 3", "mental retardation, autosomal recessive 3", "mental retardation, autosomal recessive type 3", "intellectual disability, autosomal recessive 3", "intellectual disability, autosomal recessive type 3", "autosomal recessive intellectual developmental disorder 3", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 3", "CC2D1A autosomal recessive non-syndromic intellectual disability", "autosomal recessive non-syndromic intellectual disability caused by mutation in CC2D1A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 3", "shortest_name_length": 4}
{"curie": "MONDO:0022888", "names": ["craniostenosis cataract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniostenosis cataract", "shortest_name_length": 23}
{"curie": "MONDO:0008712", "names": ["Acrocraniofacial dysostosis", "acrocraniofacial dysostosis", "ACROCRANIOFACIAL DYSOSTOSIS", "Kaplan Plauchu Fitch syndrome", "Kaplan-Plauchu-Fitch syndrome", "Acrocraniofacial dysostosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acrocraniofacial dysostosis", "shortest_name_length": 27}
{"curie": "MONDO:0002901", "names": ["Blood Type Incompatibility", "Blood type incompatibility", "Blood Group Incompatibility", "blood group incompatibility", "Incompatibility, Blood Type", "Blood Type Incompatibilities", "Incompatibility, Blood Group", "Blood Group Incompatibilities", "Incompatibilities, Blood Group"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blood group incompatibility", "shortest_name_length": 26}
{"curie": "MONDO:0030331", "names": ["RTSC4", "RITSCHER-SCHINZEL SYNDROME 4", "Ritscher-Schinzel syndrome 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ritscher-Schinzel syndrome 4", "shortest_name_length": 5}
{"curie": "MONDO:0030355", "names": ["FSHD4", "FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 4, DIGENIC", "facioscapulohumeral muscular dystrophy 4, digenic", "facioscapulohumeral muscular dystrophy 4, digenic, digenic dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "facioscapulohumeral muscular dystrophy 4, digenic", "shortest_name_length": 5}
{"curie": "MONDO:0008708", "names": ["ACS", "ACLS", "JBTS12", "Schinzel syndrome 1", "JOUBERT SYNDROME 12", "Joubert syndrome 12", "Acrocallosal Syndrome", "acrocallosal syndrome", "Acrocallosal syndrome", "ACROCALLOSAL SYNDROME", "Acrocallosal Syndromes", "Syndrome, Acrocallosal", "Syndromes, Acrocallosal", "acrocallosal syndrome (ACS)", "Schinzel acrocallosal syndrome", "SCHINZEL ACROCALLOSAL SYNDROME", "Joubert syndrome 12/15, digenic", "JOUBERT SYNDROME 12/15, DIGENIC", "Acrocallosal syndrome (disorder)", "Acrocallosal syndrome, Schinzel type", "acrocallosal syndrome, Schinzel type", "Hallux Duplication, Postaxial Polydactyly, and Absence of Corpus Callosum", "hallux Duplication, postaxial polydactyly, and absence of corpus callosum", "HALLUX DUPLICATION, POSTAXIAL POLYDACTYLY, AND ABSENCE OF CORPUS CALLOSUM", "absence of corpus callosum with unusual facial appearance, mental deficiency, duplication of the halluces and polydactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acrocallosal syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C2987483", "names": ["Stage 0 Vulvar Cancer", "Stage 0 Vulvar Carcinoma", "Stage 0 Vulvar Cancer AJCC v7", "Stage 0 Vulvar Carcinoma AJCC v7", "stage 0 vulvar carcinoma in situ"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Vulvar Cancer", "shortest_name_length": 21}
{"curie": "UMLS:C3203554", "names": ["Maternal exposure during delivery"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Maternal exposure during delivery", "shortest_name_length": 33}
{"curie": "MONDO:0006536", "names": ["CGL", "BSCL", "Seip syndrome", "SEIP SYNDROME", "Seip's syndrome", "Total lipoatrophy", "LAWRENCE SYNDROME", "Lawrence syndrome", "Total Lipodystrophy", "Total lipodystrophy", "Miescher syndrome 2", "Lipodystrophy, Total", "Berardinelli syndrome", "Lipoatrophic diabetes", "lipoatrophic diabetes", "Total Lipodystrophies", "berardinelli syndrome", "lawrence-seip syndrome", "SEIP-LAWRENCE SYNDROME", "Lipodystrophies, Total", "Lawrence-Seip syndrome", "Congenital lipo-atrophy", "Berardinelli's syndrome", "Lipodystrophy congenital", "Congenital lipodystrophy", "congenital lipodystrophy", "Generalized lipodystrophy", "Generalized Lipodystrophy", "Beradinelli-Seip syndrome", "generalized lipodystrophy", "Berardinelli-Seip syndrome", "BERARDINELLI-SEIP SYNDROME", "LIPODYSTROPHY, GENERALIZED", "Lipodystrophy, Generalized", "Berardinelli Seip Syndrome", "Berardinelli-Seip Syndrome", "Syndrome, Berardinelli-Seip", "Generalized Lipodystrophies", "Lipodystrophies, Generalized", "Lipodystrophy of Berardinelli", "Lipoatrophic diabetes mellitus", "Congenital total lipodystrophy", "lipoatrophic diabetes mellitus", "Familial lipodystrophic diabetes", "Congenital lipoatrophic diabetes", "congenital lipoatrophic diabetes", "Familial generalized lipodystrophy", "Congenital lipodystrophic diabetes", "Lawrence-Seip syndrome (diagnosis)", "familial generalized lipodystrophy", "Berardinelli-Seip-Lawrence syndrome", "Brunzell Syndrome (with Bone Cysts)", "Berardinelli lipodystrophy syndrome", "Congenital Generalized Lipodystrophy", "Syndrome, Brunzell (with Bone Cysts)", "congenital generalized lipodystrophy", "Congenital generalized lipodystrophy", "Congenital generalised lipodystrophy", "hereditary generalized lipodystrophy", "Lipodystrophy, Congenital Generalized", "Generalized Lipodystrophy, Congenital", "lipodystrophy, congenital generalized", "Congenital Generalized Lipodystrophies", "Generalized Lipodystrophies, Congenital", "Lipodystrophy with muscular hypertrophy", "Lipodystrophies, Congenital Generalized", "Congenital total lipodystrophy (disorder)", "Berardinelli-Seip Congenital Lipodystrophy", "Berardinelli-Seip congenital lipodystrophy", "Berardinelli Seip Congenital Lipodystrophy", "Lipodystrophy, Berardinelli-Seip Congenital", "Congenital Lipodystrophy, Berardinelli-Seip", "lipodystrophy-acromegaloid gigantism syndrome", "Total lipodystrophy and acromegaloid gigantism", "congenital generalized lipodystrophy (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital generalized lipodystrophy", "shortest_name_length": 3}
{"curie": "UMLS:C0159039", "names": ["spontaneous bruising", "Spontaneous bruising", "spontaneous ecchymosis", "Spontaneous ecchymosis", "Spontaneous ecchymoses", "spontaneous ecchymoses", "ecchymosis; spontaneous", "spontaneous; ecchymosis", "spontaneous bruising (symptom)", "Spontaneous bruising (disorder)", "spontaneous ecchymosis was noted", "Spontaneous ecchymosis (finding)", "spontaneous ecchymosis (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spontaneous bruising", "shortest_name_length": 20}
{"curie": "MONDO:0006616", "names": ["rhus dermatitis", "Rhus Dermatitis", "Rhus dermatitis", "Dermatitis, Rhus", "Rhus Dermatitides", "Dermatitides, Rhus", "toxicodendron dermatitis", "Toxicodendron dermatitis", "Toxicodendron Dermatitis", "Dermatitis, Toxicodendron", "Toxicodendron Dermatitides", "Dermatitides, Toxicodendron", "Contact dermatitis caused by Toxicodendron", "contact dermatitis due to genus Toxicodendron", "Contact dermatitis due to Genus Toxicodendron", "Contact dermatitis caused by urushiol from Toxicodendron", "Contact dermatitis caused by urushiol from Toxicodendron (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "toxicodendron dermatitis", "shortest_name_length": 15}
{"curie": "UMLS:C5555104", "names": ["Pharyngeal Melanoma", "Pharyngeal Mucosal Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pharyngeal Melanoma", "shortest_name_length": 19}
{"curie": "UMLS:C2987182", "names": ["Noninvasive Pancreatic Mucinous Cystic Neoplasm", "Non-Invasive Pancreatic Mucinous-Cystic Neoplasm", "Non-Invasive Pancreatic Mucinous Cystic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Invasive Pancreatic Mucinous-Cystic Neoplasm", "shortest_name_length": 47}
{"curie": "MONDO:0005841", "names": ["maxillary tumor", "MAXILLARY TUMOR", "maxillary cancer", "maxillary neoplasm", "Maxillary Neoplasm", "tumor of upper jaw", "Neoplasm, Maxillary", "Maxillary Neoplasms", "Neoplasm of maxilla", "neoplasm of maxilla", "Neoplasms, Maxillary", "upper jaw bone cancer", "bone of upper jaw tumor", "tumor of bone of upper jaw", "bone of upper jaw neoplasm", "neoplasm of bone of upper jaw", "Neoplasm of maxilla (disorder)", "neoplasm of maxilla (diagnosis)", "bone of upper jaw neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maxillary neoplasm", "shortest_name_length": 15}
{"curie": "MONDO:0032745", "names": ["DDVIBA", "DEVELOPMENTAL DELAY WITH VARIABLE INTELLECTUAL IMPAIRMENT AND BEHAVIORAL ABNORMALITIES", "developmental delay with variable intellectual impairment and behavioral abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental delay with variable intellectual impairment and behavioral abnormalities", "shortest_name_length": 6}
{"curie": "MONDO:0032832", "names": ["IDNADFS", "Chromosome 12Q15 Deletion Syndrome", "CHROMOSOME 12q15 DELETION SYNDROME", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH NASAL SPEECH, DYSMORPHIC FACIES, AND VARIABLE SKELETAL ANOMALIES", "intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies", "shortest_name_length": 7}
{"curie": "UMLS:C0332769", "names": ["Closed dislocation", "Simple Dislocation", "closed dislocation", "Simple dislocation", "Closed Dislocation", "Closed Dislocations", "CLOSED DISLOCATIONS", "Closed dislocation, NOS", "closed dislocation (diagnosis)", "Closed dislocation of unspecified location", "Closed dislocation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Closed dislocation", "shortest_name_length": 18}
{"curie": "EFO:0009276", "names": ["ventricular ectopy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ventricular ectopy", "shortest_name_length": 18}
{"curie": "MONDO:0016551", "names": ["congenital primary megaureter, refluxing form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital primary megaureter, refluxing form", "shortest_name_length": 45}
{"curie": "MONDO:0016887", "names": ["partial monosomy of chromosome 5p", "partial deletion of chromosome 5p", "partial monosomy of the short arm of chromosome 5", "partial deletion of the short arm of chromosome 5", "partial deletion of the short arm of chromosome type 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of the short arm of chromosome 5", "shortest_name_length": 33}
{"curie": "MONDO:0012443", "names": ["ANIB4", "intracranial berry aneurysm 4", "aneurysm, intracranial BERRY, 4", "ANEURYSM, INTRACRANIAL BERRY, 4", "Aneurysm, Intracranial Berry, 4", "aneurysm, intracranial berry, 4", "ANEURYSM, INTRACRANIAL BERRY, 4 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aneurysm, intracranial berry, 4", "shortest_name_length": 5}
{"curie": "UMLS:C5554923", "names": ["Acute Radiation Skin Toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Radiation Skin Toxicity", "shortest_name_length": 29}
{"curie": "MONDO:0021654", "names": ["mucinosis skin", "Mucinosis of skin", "Mucinosis of the skin", "mucinosis skin (diagnosis)", "diffuse cutaneous mucinosis", "Diffuse cutaneous mucinosis", "Diffuse cutaneous mucinosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diffuse cutaneous mucinosis", "shortest_name_length": 14}
{"curie": "UMLS:C0346168", "names": ["Benign Ovarian Epithelial Tumor", "Benign Epithelial Tumor of Ovary", "Benign epithelial tumor of ovary", "Benign epithelial tumour of ovary", "Benign Ovarian Epithelial Neoplasm", "Benign Epithelial Neoplasm of Ovary", "benign epithelial neoplasm of ovary", "Benign Epithelial Tumor of the Ovary", "OVARY, BENIGN SURFACE EPITHELIAL TUMOR", "Benign Epithelial Neoplasm of the Ovary", "Benign Ovarian Surface Epithelial Tumor", "Benign Surface Epithelial Tumor of Ovary", "Benign Ovarian Surface Epithelial Neoplasm", "Benign epithelial tumor of ovary (disorder)", "Benign Surface Epithelial Neoplasm of Ovary", "Benign Surface Epithelial Tumor of the Ovary", "Benign Ovarian Surface Epithelial-Stromal Tumor", "Benign Surface Epithelial Neoplasm of the Ovary", "benign epithelial neoplasm of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign epithelial tumor of ovary", "shortest_name_length": 31}
{"curie": "MONDO:0007380", "names": ["LCD", "CDL1", "Lcd1", "LCDI", "LCD1", "Biber-Haab-Dimmer Dystrophy", "Biber-Haab-Dimmer dystrophy", "lattice corneal dystrophy type I", "lattice corneal dystrophy type 1", "Lattice corneal dystrophy Type I", "Lattice Corneal Dystrophy Type I", "LCD1 Lattice Corneal Dystrophy 1", "Lattice corneal dystrophy type 1", "Lattice corneal dystrophy type I", "CORNEAL DYSTROPHY, LATTICE TYPE I", "corneal dystrophy, lattice type 1", "Corneal Dystrophy, Lattice Type I", "Corneal dystrophy, lattice type 1", "corneal dystrophy, lattice type I", "Lattice Corneal Dystrophy, Type I", "LATTICE CORNEAL DYSTROPHY, TYPE I", "classic lattice corneal dystrophy", "Classic lattice corneal dystrophy", "lattice corneal dystrophy, type I", "lattice corneal dystrophy, type 1", "CDL1 Corneal dystrophy, lattice type 1", "Lattice corneal dystrophy Type I (disorder)", "lattice corneal dystrophy, type I (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lattice corneal dystrophy type I", "shortest_name_length": 3}
{"curie": "MONDO:0020791", "names": ["MECD1", "Meesmann Corneal Dystrophy", "Meesmann corneal dystrophy 1", "meesmann corneal dystrophy 1", "CORNEAL DYSTROPHY, MEESMANN, 1", "corneal dystrophy, Meesmann, 1", "Corneal Dystrophy, Meesmann Epithelial", "Corneal Dystrophy, Juvenile Epithelial, of Meesmann"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal dystrophy, Meesmann, 1", "shortest_name_length": 5}
{"curie": "MONDO:0054573", "names": ["LOMARS", "Lopes-Maciel-Rodan syndrome", "LOPES-MACIEL-RODAN SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lopes-Maciel-Rodan syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0014482", "names": ["MRD29", "SETBP1 disorder", "SETBP1-related disorder", "SETBP1 related developmental delay", "SETBP1-related intellectual disability", "autosomal dominant mental retardation 29", "mental retardation, autosomal dominant 29", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 29", "autosomal dominant intellectual disability 29", "mental retardation, autosomal dominant type 29", "intellectual disability, autosomal dominant 29", "intellectual disability, autosomal dominant type 29", "autosomal dominant intellectual developmental disorder 29", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 29", "autosomal dominant non-syndromic intellectual disability 29", "SETBP1 intellectual disability-expressive aphasia-facial dysmorphism syndrome", "intellectual disability-expressive aphasia-facial dysmorphism syndrome caused by mutation in SETBP1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 29", "shortest_name_length": 5}
{"curie": "MONDO:0001479", "names": ["cutaneous diphteria", "Cutaneous Diphtheria", "cutaneous diphtheria", "Cutaneous diphtheria", "diphtheria; cutaneous", "Diphtheria, cutaneous", "DIPHTHERIA, CUTANEOUS", "cutaneous; diphtheritic", "Cutaneous diphtheria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous diphtheria", "shortest_name_length": 19}
{"curie": "MONDO:0009514", "names": ["LMS", "LNMS", "Laurence-Moon", "Laurence Moon Syndrome", "LAURENCE-MOON SYNDROME", "laurence moon syndrome", "laurence-moon syndrome", "Laurence-MOON syndrome", "Laurence-Moon syndrome", "Laurence-Moon Syndrome", "Syndrome, Laurence-Moon", "Laurence Moon Biedl Syndrome", "LAURENCE-MOON-BIEDL SYNDROME", "laurence moon biedl syndrome", "Laurence-Moon-Biedl Syndrome", "laurence-moon-biedl syndrome", "Lawrence Moon Biedl Syndrome", "biedl laurence moon syndrome", "Laurence-Moon-Biedl syndrome", "biedl lawrence moon syndrome", "lawrence moon biedl syndrome", "Laurence Moon Biedl syndrome", "Syndrome, Laurence-Moon-Biedl", "Laurence-Moon syndrome (disorder)", "Laurence-Moon syndrome (diagnosis)", "Laurence-Moon-Biedl syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laurence-Moon syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C4528617", "names": ["Stage IA Vulvar Cancer", "Stage IA Vulvar Cancer AJCC v8", "Stage IA Vulvar Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Vulvar Cancer AJCC v8", "shortest_name_length": 22}
{"curie": "MONDO:0017622", "names": ["CSID without sucrose intolerance", "disaccharide intolerance without sucrose intolerance", "congenital sucrase-isomaltase deficiency without sucrose intolerance", "congenital sucrose-isomaltose malabsorption without sucrose intolerance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital sucrase-isomaltase deficiency without sucrose intolerance", "shortest_name_length": 32}
{"curie": "UMLS:C0861772", "names": ["Rectal cancer Dukes D", "Dukes D rectal cancer", "stage IV rectum cancer", "rectum cancer, Dukes D", "Rectal cancer stage IV", "rectal cancer, Dukes D", "stage IV rectal cancer", "rectum cancer, stage IV", "rectal cancer, stage IV", "metastatic rectum cancer", "Rectal cancer metastatic", "metastatic rectal cancer", "Rectal carcinoma stage IV", "rectum cancer, metastatic", "Carcinoma rectum stage IV", "rectal cancer, metastatic", "Carcinoma of rectum stage IV", "Astler-Coller D rectal cancer", "rectum cancer, Astler-Coller D", "rectal cancer, Astler-Coller D"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rectal cancer stage IV", "shortest_name_length": 21}
{"curie": "MONDO:0011963", "names": ["JBTS2", "CORS2", "Joubert syndrome 2", "JOUBERT SYNDROME 2", "Joubert syndrome type 2", "TMEM216 Joubert syndrome", "Cerebellooculorenal syndrome 2", "CEREBELLOOCULORENAL SYNDROME 2", "cerebellooculorenal syndrome 2", "Joubert syndrome caused by mutation in TMEM216"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome 2", "shortest_name_length": 5}
{"curie": "UMLS:C1336201", "names": ["Stage IIC Retinoblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIC Retinoblastoma", "shortest_name_length": 24}
{"curie": "UMLS:C1707410", "names": ["Clear Cell Variant Thyroid Gland Papillary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clear Cell Variant Thyroid Gland Papillary Carcinoma", "shortest_name_length": 52}
{"curie": "MONDO:0008178", "names": ["MSP1", "IBMPFD1", "MULTISYSTEM PROTEINOPATHY 1", "multisystem proteinopathy 1", "pagetoid amyotrophic lateral sclerosis", "muscular dystrophy, limb-girdle, with Paget disease of bone", "lower motor neuron degeneration with Paget-like bone disease", "Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia", "inclusion body myopathy with early-onset paget disease and frontotemporal dementia 1", "inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1", "INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 1", "Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 1", "inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1", "inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia type 1", "inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1", "shortest_name_length": 4}
{"curie": "MONDO:0016816", "names": ["Leigh disease with nephrotic syndrome", "Leigh syndrome with nephrotic syndrome", "infantile subacute necrotizing encephalopathy with nephrotic syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leigh syndrome with nephrotic syndrome", "shortest_name_length": 37}
{"curie": "MONDO:0007513", "names": ["Ectodermal dysplasia adrenal cyst", "Ectodermal Dysplasia with Adrenal Cyst", "Adrenal cyst with ectodermal dysplasia", "ectodermal dysplasia with adrenal cyst", "ECTODERMAL DYSPLASIA WITH ADRENAL CYST", "Odonto-onycho-hypohidrotic dysplasia-midline scalp defects syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia with adrenal cyst", "shortest_name_length": 33}
{"curie": "MONDO:0019462", "names": ["SMZL", "SLVL", "splenic marginal zone lymphoma", "marginal zone splenic lymphoma", "Splenic Marginal Zone Lymphoma", "Marginal zone lymphoma, spleen", "lymphoma splenic marginal zone", "Splenic marginal zone lymphoma", "Splenic marginal zone lymphomas", "Marginal zone lymphoma of spleen", "marginal zone lymphoma of spleen", "Marginal Zone Lymphoma of Spleen", "Splenic marginal zone lymphoma NOS", "Splenic marginal zone lymphoma, NOS", "Marginal Zone Lymphoma of the Spleen", "marginal zone lymphoma of the spleen", "splenic marginal zone B-cell lymphoma", "Splenic marginal zone B-cell lymphoma", "Splenic Marginal Zone B-Cell Lymphoma", "Marginal zone lymphoma involving spleen", "marginal zone B-cell lymphoma of spleen", "Splenic lymphoma with villous lymphocytes", "Marginal zone lymphoma of spleen (disorder)", "marginal zone lymphoma of spleen (diagnosis)", "Splenic marginal zone B-cell lymphoma (disorder)", "marginal zone B-cell lymphoma of spleen (diagnosis)", "Splenic lymphoma with villous lymphocytes (disorder)", "splenic lymphoma with circulating villous lymphocytes", "Splenic lymphoma with villous lymphocytes (diagnosis)", "Splenic Lymphoma with Circulating Villous Lymphocytes", "Splenic Marginal Zone Lymphoma with Villous Lymphocytes", "splenic marginal zone lymphoma with villous lymphocytes", "leukemia lymphocytic chronic splenic with villous lymphocytes", "splenic marginal zone B-cell lymphoma with villous lymphocytes", "Splenic Marginal Zone B-Cell Lymphoma with Villous Lymphocytes", "Splenic marginal zone B-cell lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "splenic marginal zone lymphoma", "shortest_name_length": 4}
{"curie": "UMLS:C0751514", "names": ["Verbal Fluency Disorder", "Verbal Fluency Disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Verbal Fluency Disorders", "shortest_name_length": 23}
{"curie": "MONDO:0007759", "names": ["FCHL", "FCHL3", "MIXED HYPERLIPIDEMIA", "mixed hyperlipidemia", "mixed hyperlipidaemia", "Type IIb Hyperlipidemia", "Hyperlipidemia Type IIb", "Type IIb hyperlipidemia", "Type IIb hyperlipidaemia", "Hyperapobetalipoproteinemia", "Hyperapobetalipoproteinaemia", "Multiple-type hyperlipidemia", "disorder hyperlipidemia mixed", "Multiple-type hyperlipidaemia", "type IIb hyperlipoproteinemia", "Type IIb Hyperlipoproteinemia", "Hyperlipoproteinemia, Type IIb", "FAMILIAL COMBINED HYPERLIPIDEMIA", "familial combined hyperlipidemia", "Familial combined hyperlipidemia", "Familial Combined Hyperlipidemia", "combined hyperlipidemia, familial", "hyperlipidemia; familial combined", "Familial combined hyperlipidaemia", "Familial Combined Hyperlipidemias", "Combined Hyperlipidemia, Familial", "hyperlipidemia, familial combined", "Hyperlipidemia, Familial Combined", "Hyperlipidemias, Familial Combined", "Combined Hyperlipidemias, Familial", "familial; hyperlipidemia, combined", "broad floating betalipoproteinemia", "HYPERLIPIDEMIA, FAMILIAL COMBINED, 3", "Familial hyperlipoproteinemia type IIb", "Familial hyperlipoproteinaemia type IIb", "FCHL - Familial combined hyperlipidemia", "FCHL (familial combined hyperlipidemia)", "FCHL - Familial combined hyperlipidaemia", "Multiple Lipoprotein-Type Hyperlipidemia", "Fredrickson type IIb hyperlipoproteinemia", "Hyperlipidemia, Multiple Lipoprotein-Type", "Lipoprotein-Type Hyperlipidemia, Multiple", "Hyperlipidemia, Multiple Lipoprotein Type", "Multiple Lipoprotein-Type Hyperlipidemias", "Fredrickson type IIb hyperlipoproteinaemia", "Hyperlipidemias, Multiple Lipoprotein-Type", "Lipoprotein-Type Hyperlipidemias, Multiple", "Familial combined hyperlipidemia (disorder)", "familial combined hyperlipidemia (diagnosis)", "hyperlipidemia, familial combined, LPL related", "familial multiple lipoprotein-type hyperlipidemia", "Familial multiple lipoprotein-type hyperlipidemia", "Familial multiple lipoprotein-type hyperlipidaemia", "hyperbetalipoproteinemia with prebetalipoproteinemia", "Familial multiple lipoprotein-type hyperlipidemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperlipidemia, familial combined, LPL related", "shortest_name_length": 4}
{"curie": "MONDO:0012102", "names": ["JOAG3", "GLC1K", "JOAG1K", "GLAUCOMA 1, OPEN ANGLE, K", "Glaucoma 1, Open Angle, K", "glaucoma 1, open angle, K", "Glaucoma, Primary Open Angle, Juvenile-Onset, 3", "glaucoma 1K, primary open angle, juvenile-onset", "GLAUCOMA, PRIMARY OPEN ANGLE, JUVENILE-ONSET, 3", "glaucoma, primary open angle, juvenile-onset, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glaucoma 1, open angle, K", "shortest_name_length": 5}
{"curie": "OMIM:601696", "names": ["NOVELTY SEEKING PERSONALITY TRAIT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 33}
{"curie": "MONDO:0008050", "names": ["MPD1", "Gowers disease", "distal myopathy 1", "Distal 1 Myopathy", "Distal Myopathy 1", "Myopathy 1, Distal", "Distal Myopathy 1s", "Myopathy, Distal 1", "MYOPATHY, DISTAL, 1", "myopathy, distal, 1", "Myopathy 1s, Distal", "Distal 1 Myopathies", "Myopathies, Distal 1", "Laing distal myopathy", "LAING DISTAL MYOPATHY", "Laing Distal Myopathy", "Distal myopathy type 1", "distal myopathy type 1", "Distal Myopathy, Laing", "Myopathy, Laing Distal", "myopathy distal, type 1", "myosin storage myopathy", "myopathy, distal, type 1", "MYH7-related skeletal myopathy", "Myopathy, Late Distal Hereditary", "myopathy, late distal hereditary", "MYOPATHY, LATE DISTAL HEREDITARY", "Laing Early-Onset Distal Myopathy", "Laing early-onset distal myopathy", "distal myopathy laing early-onset", "Laing Early Onset Distal Myopathy", "Laing early-onset distal myopathy (disorder)", "Laing early-onset distal myopathy (diagnosis)", "MYOPATHY, DISTAL, EARLY-ONSET, AUTOSOMAL DOMINANT", "myopathy, distal, early-onset, autosomal dominant", "Myopathy, Distal, Early-Onset, Autosomal Dominant", "Muscular Dystrophy, Distal, Late-Onset, Autosomal Dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MYH7-related skeletal myopathy", "shortest_name_length": 4}
{"curie": "MONDO:0032580", "names": ["NPHS17", "nephrotic syndrome type 17", "NEPHROTIC SYNDROME, TYPE 17", "nephrotic syndrome, type 17"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrotic syndrome, type 17", "shortest_name_length": 6}
{"curie": "UMLS:C1335255", "names": ["Stage 1 Hepatoblastoma", "PRETEXT Stage 1 Hepatoblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PRETEXT Stage 1 Hepatoblastoma", "shortest_name_length": 22}
{"curie": "MONDO:0001603", "names": ["Paralytic lagophthalmos", "Paralytic Lagophthalmos", "paralytic lagophthalmos", "Lagophthalmos, Paralytic", "Paralytic lagophthalmos (finding)", "paralytic lagophthalmos (disease)", "paralytic lagophthalmos (diagnosis)", "paralytic lagophthalmos was observed", "paralytic lagophthalmos (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paralytic lagophthalmos", "shortest_name_length": 23}
{"curie": "MONDO:0015816", "names": ["indolent primary cutaneous T-cell lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "indolent primary cutaneous T-cell lymphoma", "shortest_name_length": 42}
{"curie": "MONDO:0015683", "names": ["primary malignant peritoneal tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary malignant peritoneal tumor", "shortest_name_length": 34}
{"curie": "UMLS:C4525142", "names": ["Stage IVA Rectal Cancer", "Stage IVA Rectal Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Rectal Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "MONDO:0019146", "names": ["MSMD", "Familial Atypical Mycobacteriosis", "Familial Atypical Mycobacterioses", "Atypical Mycobacteriosis, Familial", "Mycobacterioses, Familial Atypical", "Mycobacteriosis, Familial Atypical", "Atypical Mycobacterial Infection, Disseminated", "Atypical Mycobacteriosis, Familial Disseminated", "Mendelian susceptibility to atypical mycobacteria", "Mendelian susceptibility to mycobacterial diseases", "inherited susceptibility to mycobacterial diseases", "Mendelian susceptibility to mycobacterial infections", "Atypical Mycobacterial Infection, Familial Disseminated", "Idiopathic infection caused by BCG or atypical mycobacteria", "idiopathic infection caused by BCG or atypical mycobacteria", "Mycobacterium genetic susceptibility to infections due to particular pathogens", "Mycobacterium caused genetic susceptibility to infections due to particular pathogens"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited susceptibility to mycobacterial diseases", "shortest_name_length": 4}
{"curie": "UMLS:C4682755", "names": ["IVA", "stage IVA prostate cancer", "Stage IVA Prostate Cancer", "Stage IVA Prostate Cancer AJCC v8", "stage IVA prostate cancer AJCC v8", "stage IVA prostate carcinoma AJCC v8", "Stage IVA Prostate Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Prostate Cancer AJCC v8", "shortest_name_length": 3}
{"curie": "UMLS:C1516433", "names": ["Cervical Squamotransitional Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Squamotransitional Carcinoma", "shortest_name_length": 37}
{"curie": "UMLS:C0854799", "names": ["B precursor type acute leukemia", "B precursor type acute leukaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B precursor type acute leukemia", "shortest_name_length": 31}
{"curie": "MONDO:0000385", "names": ["benign GI tumor", "Benign GI Tumor", "Benign GI Neoplasm", "benign GI neoplasm", "GI NEOPLASM BENIGN", "GI neoplasm benign", "Benign GI System Tumor", "Benign GI tract tumors", "benign GI system tumor", "Non-cancerous GI tumors", "Benign GI tract tumours", "Non-cancerous GI tumours", "Benign Tumor of GI System", "Benign GI System Neoplasm", "benign tumor of GI system", "Neoplasm benign;digestive", "benign GI system neoplasm", "benign digestive system tumor", "Benign Digestive System Tumor", "benign tumor of the GI system", "Benign Tumor of the GI System", "Benign Gastrointestinal Tumor", "benign gastrointestinal tumor", "benign tumor of digestive tract", "Benign gastrointestinal neoplasm", "benign digestive system neoplasm", "benign gastrointestinal neoplasm", "Benign Tumor of Digestive System", "benign tumor of digestive system", "Benign Digestive System Neoplasm", "Benign Gastrointestinal Neoplasm", "Gastrointestinal neoplasms benign", "Benign digestive system neoplasms", "Benign neoplasms gastrointestinal", "benign neoplasm of digestive tract", "Benign Neoplasm of Digestive System", "benign neoplasm of digestive system", "Benign gastrointestinal neoplasm NOS", "Benign gastrointestinal tract tumors", "benign gastrointestinal system tumor", "benign tumor of the digestive system", "Benign Tumor of the Digestive System", "Benign Gastrointestinal System Tumor", "Benign gastrointestinal tract tumours", "Benign tumor of gastrointestinal tract", "gastrointestinal system benign neoplasm", "Benign tumour of gastrointestinal tract", "benign tumor of gastrointestinal system", "benign neoplasm of the digestive system", "Benign Tumor of Gastrointestinal System", "Benign neoplasm of digestive system NOS", "Benign Neoplasm of the Digestive System", "Benign neoplasm of gastrointestinal tract", "Benign Neoplasm of Gastrointestinal System", "benign neoplasm of gastrointestinal system", "Benign Tumor of the Gastrointestinal System", "benign tumor of the gastrointestinal system", "Neoplasm digestive system benign/unspecified", "Benign neoplasm of gastrointestinal tract NOS", "benign neoplasm of digestive tract (diagnosis)", "Benign neoplasm of gastrointestinal tract, NOS", "Benign neoplasm of other parts of digestive system", "Benign neoplasm of gastrointestinal tract (disorder)", "alimentary part of gastrointestinal system benign neoplasm", "Benign neoplasm of other and unspecified site in the digestive system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign digestive system neoplasm", "shortest_name_length": 15}
{"curie": "UMLS:C3273073", "names": ["Liver Lymphangioma", "Lymphangioma of liver", "Lymphangioma of liver (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphangioma of liver", "shortest_name_length": 18}
{"curie": "MONDO:0000625", "names": ["Reproductive neoplasms male benign", "Benign Male Reproductive System Tumor", "benign Male reproductive system tumor", "Benign male reproductive tract neoplasm", "male reproductive organ benign neoplasm", "Benign Male Reproductive System Neoplasm", "benign Male reproductive system neoplasm", "benign male reproductive system neoplasm", "Benign male reproductive tract neoplasm NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign male reproductive system neoplasm", "shortest_name_length": 34}
{"curie": "UMLS:C0948840", "names": ["Meningeal leukemia", "Meningeal Leukemia", "meningeal leukemia", "leukemia meningeal", "Leukemic meningitis", "leukemic meningitis", "Leukemic Meningitis", "Meningeal leukaemia", "meningitis, leukemic", "Leukaemic meningitis", "Leukemic Leptomeningitis", "Leukemic leptomeningitis", "leukemic leptomeningitis", "Leukaemic leptomeningitis", "meningitis, carcinomatous", "leptomeningitis, leukemic", "Meningeal leukemia (disorder)", "Meningeal leukemia (diagnosis)", "leukemic meningitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meningeal Leukemia", "shortest_name_length": 18}
{"curie": "MONDO:0000710", "names": ["upper GI Crohn's disease", "gastroduodenal Crohn disease", "gastroduodenal Crohn's disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastroduodenal Crohn disease", "shortest_name_length": 24}
{"curie": "MONDO:0010042", "names": ["spastic diplegia infantile type", "Spastic diplegia infantile type", "spastic diplegia, infantile type", "Spastic Diplegia, Infantile Type", "SPASTIC DIPLEGIA, INFANTILE TYPE", "SPASTIC DIPLEGIA AND MENTAL RETARDATION", "spastic diplegia and mental retardation", "spastic diplegia and intellectual disability", "hereditary spastic diplegia with mental retardation", "Hereditary spastic diplegia with mental retardation", "SPASTIC DIPLEGIA AND IMPAIRED INTELLECTUAL DEVELOPMENT", "hereditary spastic diplegia with intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic diplegia and intellectual disability", "shortest_name_length": 31}
{"curie": "MONDO:0015547", "names": ["genetic dementia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genetic dementia", "shortest_name_length": 16}
{"curie": "UMLS:C0334544", "names": ["Hemolymphangioma", "hemolymphangioma", "Haemolymphangioma", "Lymphangioma with Hemorrhage", "Hemolymphangioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemolymphangioma", "shortest_name_length": 16}
{"curie": "UMLS:C1708240", "names": ["Germinative Follicular Epithelium Tumor", "Germinative Follicular Epithelium Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Germinative Follicular Epithelium Neoplasm", "shortest_name_length": 39}
{"curie": "UMLS:C5204785", "names": ["Advanced Thymic Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Thymic Carcinoma", "shortest_name_length": 25}
{"curie": "UMLS:C0434165", "names": ["ovary injury", "ovary; injury", "injury; ovary", "Ovarian Injury", "Ovarian injury", "injury of ovary", "Injury of Ovary", "Injury of ovary", "Injury of ovary (disorder)", "injury of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of ovary", "shortest_name_length": 12}
{"curie": "MONDO:0001629", "names": ["Jaccoud", "Jaccoud syndrome", "Jaccoud's disease", "jaccoud's syndrome", "Jaccoud's syndrome", "Jaccoud's arthritis", "jaccoud's arthritis", "Jaccoud; arthropathy", "arthropathy; Jaccoud", "Jaccoud's arthropathy", "Jaccoud's syndrome (disorder)", "Chronic postrheumatic arthritis", "Chronic postrheumatic arthropathy", "Non-deforming erosive arthropathy", "chronic postrheumatic arthropathy", "Chronic post rheumatic arthropathy", "Chronic post - rheumatic arthropathy", "Chronic postrheumatic arthropathy [Jaccoud]", "chronic postrheumatic arthropathy (diagnosis)", "Chronic postrheumatic arthropathy [Jaccoud], unspecified site", "Chronic postrheumatic arthropathy [Jaccoud], site unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jaccoud syndrome", "shortest_name_length": 7}
{"curie": "MONDO:0041751", "names": ["MB leprosy", "lepromatous leprosy", "Multibacillary Leprosy", "multibacillary leprosy", "Multibacillary leprosy", "Borderline Lepromatous", "leprosy multibacillary", "Leprosy, Multibacillary", "Lepromatous, Borderline", "Multibacillary Leprosies", "Midborderline Lepromatous", "Leprosies, Multibacillary", "Lepromatous, Midborderline", "Multibacillary leprosy (disorder)", "Multibacillary leprosy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multibacillary leprosy", "shortest_name_length": 10}
{"curie": "MONDO:0024674", "names": ["Pancoast", "Pancoast tumor", "tumor, Pancoast", "PANCOAST SYNDROME", "pancoast syndrome", "Pancoast Syndrome", "Pancoast syndrome", "pancoasts syndrome", "Pancoasts syndrome", "Pancoasts Syndrome", "Syndrome, Pancoast", "syndrome, Pancoast", "Pancoast's syndrome", "Pancoast's Syndrome", "pancoast's syndrome", "Syndrome, Pancoast's", "syndrome, Pancoast's", "Pancoast's syndrome (disorder)", "superior pulmonary sulcus syndrome", "Superior pulmonary sulcus syndrome", "SUPERIOR PULMONARY SULCUS SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancoast syndrome", "shortest_name_length": 8}
{"curie": "MONDO:0020340", "names": ["bilateral perisylvian polymicrogyria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bilateral perisylvian polymicrogyria", "shortest_name_length": 36}
{"curie": "UMLS:C4553782", "names": ["Stage 0a Renal Pelvis Cancer", "Stage 0a Renal Pelvis Cancer AJCC v8", "Stage 0a Renal Pelvis Urothelial Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0a Renal Pelvis Cancer AJCC v8", "shortest_name_length": 28}
{"curie": "MONDO:0006931", "names": ["SPN", "Coin Lesion", "coin lesion lung", "lung coin lesion", "Coin lesion lung", "coin lung lesion", "Lesion;coin;lung", "coin lesion of lung", "Coin lesion of lung", "Solitary Lung Nodule", "Nodule, Solitary Lung", "pulmonary coin lesion", "Lung Nodule, Solitary", "Solitary Lung Nodules", "Pulmonary Coin Lesion", "Coin Lesion, Pulmonary", "Pulmonary Coin Lesions", "pulmonary coin lesions", "Lesion, Pulmonary Coin", "Solitary nodule of lung", "Coin Lesions, Pulmonary", "solitary pulmonary nodule", "Solitary pulmonary nodule", "PULMONARY NODULE SOLITARY", "Solitary Pulmonary Nodule", "Solitary Pulmonary Nodules", "Pulmonary Nodule, Solitary", "Nodule, Solitary Pulmonary", "solitary pulmonary nodules", "Nodules, Solitary Pulmonary", "Pulmonary Nodules, Solitary", "coin lesion of lung (finding)", "Coin lesion of lung (finding)", "Solitary nodule of lung (finding)", "solitary pulmonary nodule (procedure)", "coin lesion of lung (context-dependent category)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary coin lesion", "shortest_name_length": 3}
{"curie": "MONDO:0013421", "names": ["C8D2", "C8B DEFICIENCY", "C8B deficiency", "C8 Beta deficiency", "C8 BETA DEFICIENCY", "C8 deficiency type II", "C8 deficiency, type 2", "C8 DEFICIENCY, TYPE II", "C8 deficiency, type II", "COMPLEMENT COMPONENT 8B DEFICIENCY", "complement component 8B deficiency", "Human complement C8-beta deficiency", "complement component 8 deficiency type 2", "complement component 8 deficiency, type 2", "type II complement component 8 deficiency", "complement component 8 deficiency type II", "complement component 8 deficiency, type II", "COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II", "C8B classic complement early component deficiency", "classic complement early component deficiency caused by mutation in C8B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type II complement component 8 deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0017337", "names": ["inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency", "Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency", "Inherited isolated adrenal insufficiency due to partial cytochrome P450 family 11 subfamily A member 1 deficiency", "Inherited isolated adrenal insufficiency due to partial cytochrome P450 family 11 subfamily A member 1 deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency", "shortest_name_length": 74}
{"curie": "UMLS:C1334942", "names": ["Neoplastic PTLD", "Post-Transplant Lymphocytic Neoplasm", "Post-Transplant Lymphoproliferative Neoplasm", "Post-Transplant Neoplastic Lymphoproliferative Disorder", "Neoplastic Post-Transplant Lymphoproliferative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplastic Post-Transplant Lymphoproliferative Disorder", "shortest_name_length": 15}
{"curie": "MONDO:0005312", "names": ["pouchitis", "Pouchitis", "Pouch Ileitis", "Ileitis, Pouch", "pouchitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pouchitis", "shortest_name_length": 9}
{"curie": "MONDO:0001374", "names": ["sarcoma bladder", "bladder sarcoma", "Bladder Sarcoma", "sarcoma of bladder", "Sarcoma of bladder", "Sarcoma of Bladder", "sarcoma of the bladder", "Sarcoma of the Bladder", "Urinary bladder sarcoma", "Urinary Bladder Sarcoma", "urinary bladder sarcoma", "sarcoma of urinary bladder", "Sarcoma of Urinary Bladder", "Sarcoma of bladder (disorder)", "sarcoma of bladder (diagnosis)", "sarcoma of the urinary bladder", "Sarcoma of the Urinary Bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder sarcoma", "shortest_name_length": 15}
{"curie": "MONDO:0044333", "names": ["Alcoholic Korsakoff Syndrome", "Korsakoff Syndrome, Alcoholic", "Alcoholic Korsakoff's Psychosis", "alcoholic Korsakoff's psychosis", "alcohol-induced amnestic syndrome", "Alcohol-Induced Amnestic Syndrome", "Alcohol Induced Korsakoff Syndrome", "Alcohol-Induced Korsakoff Syndrome", "Korsakoff Syndrome, Alcohol-Induced", "Alcoholic Wernicke-Korsakoff Syndrome", "alcoholic Wernicke-Korsakoff syndrome", "Alcoholic Wernicke Korsakoff Syndrome", "Wernicke-Korsakoff Syndrome, Alcoholic", "Wernicke-Korsakoff syndrome, alcoholic", "alcoholic Wernicke-Korsakoff psychosis", "Alcohol-Induced Wernicke-Korsakoff's Syndrome", "alcohol-induced Wernicke-Korsakoff's syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alcohol-induced Wernicke-Korsakoff's syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0700089", "names": ["PDC", "FPD1", "DYT8", "PNKD1", "PxMD-PNKD", "Dystonia 8", "dystonia 8", "DYSTONIA 8", "mount-reback syndrome", "MOUNT-REBACK SYNDROME", "Mount-Reback syndrome", "PNKD paroxysmal dyskinesia", "Nonkinesigenic choreoathetosis", "CHOREOATHETOSIS, NONKINESIGENIC", "choreoathetosis, nonkinesigenic", "Choreoathetosis, Nonkinesigenic", "Familial paroxysmal choreoathetosis", "Choreoathetosis familial paroxysmal", "PAROXYSMAL DYSTONIC CHOREOATHETOSIS", "paroxysmal dystonic choreoathetosis", "Paroxysmal dystonic choreoathetosis", "Paroxysmal nonkinesigenic dyskinesia", "CHOREOATHETOSIS, FAMILIAL PAROXYSMAL", "Choreoathetosis, Familial Paroxysmal", "choreoathetosis, familial paroxysmal", "paroxysmal nonkinesigenic dyskinesia 1", "PAROXYSMAL NONKINESIGENIC DYSKINESIA 1", "Paroxysmal Nonkinesigenic Dyskinesia 1", "paroxysmal nonkinesigenic dyskinesia type 1", "Familial Paroxysmal Nonkinesigenic Dyskinesia", "paroxysmal dyskinesia caused by mutation in PNKD"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paroxysmal nonkinesigenic dyskinesia 1", "shortest_name_length": 3}
{"curie": "UMLS:C0347721", "names": ["strain back", "back strain", "Back strain", "BACK STRAIN", "Strain;back", "back strains", "back strained", "strain of back", "muscle pull back", "back muscle pull", "muscle pulled back", "Pulled back muscle", "muscle strain back", "back pulled muscle", "back muscle pulled", "pulled back muscle", "back muscle strain", "Strain of back, NOS", "back muscles pulled", "back muscle strains", "back muscle strained", "back muscles strained", "Strain of back muscle", "strain of back (diagnosis)", "Strain of back muscle (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Strain of back muscle", "shortest_name_length": 11}
{"curie": "UMLS:C4521626", "names": ["Stage IV Sinonasal Cancer AJCC v8", "Stage IV Sinonasal Carcinoma AJCC v8", "Stage IV Nasal Cavity and Paranasal Sinus Cancer", "Stage IV Nasal Cavity and Paranasal Sinus Cancer AJCC v8", "Stage IV Nasal Cavity and Paranasal Sinus Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Nasal Cavity and Paranasal Sinus Cancer AJCC v8", "shortest_name_length": 33}
{"curie": "UMLS:C4727142", "names": ["Locally Advanced Unresectable Malignant Tumor", "Locally Advanced Unresectable Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Unresectable Malignant Neoplasm", "shortest_name_length": 45}
{"curie": "MONDO:0015739", "names": ["Adult-onset nemaline myopathy", "adult-onset nemaline myopathy", "Adult Onset Nemaline Myopathy", "Nemaline myopathy, adult onset", "Nemaline Myopathy, Adult Onset", "Nemaline myopathy, late onset type", "Nemaline myopathy, late onset type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult-onset nemaline myopathy", "shortest_name_length": 29}
{"curie": "MONDO:0019719", "names": ["CAKUT", "Cakut", "renal or urinary tract malformation", "Renal or urinary tract malformation", "congenital anomaly of kidney and urinary tract", "Congenital Anomalies Of Kidney And Urinary Tract", "congenital anomalies of kidney and urinary tract", "Congenital anomalies of kidney and urinary tract", "Congenital anomalies of the kidney and urinary tract", "congenital anomalies of the kidney and urinary tract", "Congenital anomalies of the kidney and urinary tract (CAKUT)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital anomaly of kidney and urinary tract", "shortest_name_length": 5}
{"curie": "UMLS:C5446667", "names": ["Locally Invasive Desmoid-Type Fibromatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Invasive Desmoid-Type Fibromatosis", "shortest_name_length": 42}
{"curie": "MONDO:0010801", "names": ["SPONDYLOCAMPTODACTYLY", "spondylocamptodactyly", "Spondylocamptodactyly", "spondylocamptodactyly syndrome", "Spondylocamptodactyly syndrome", "spondylo camptodactyly syndrome", "Spondylo camptodactyly syndrome", "Spondylocamptodactyly syndrome (disorder)", "Camptodactyly with cervical platyspondyly", "camptodactyly with cervical platyspondyly", "CAMPTODACTYLY WITH CERVICAL PLATYSPONDYLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondylocamptodactyly syndrome", "shortest_name_length": 21}
{"curie": "UMLS:C2981379", "names": ["Stage IIB Small Intestinal Cancer", "Stage IIB Small Intestinal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Small Intestinal Cancer AJCC v7", "shortest_name_length": 33}
{"curie": "UMLS:C4524715", "names": ["Clinical Stage IIB Gastroesophageal Junction Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage IIB Gastroesophageal Junction Adenocarcinoma AJCC v8", "shortest_name_length": 67}
{"curie": "UMLS:C0280160", "names": ["Stage III Diffuse Small Cleaved Cell Lymphoma", "Adult Diffuse Small Cleaved Cell Lymphoma Stage III", "stage III adult diffuse small cleaved cell lymphoma", "Stage III Adult Diffuse Small Cleaved Cell Lymphoma", "adult diffuse small cleaved cell lymphoma, stage III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Adult Diffuse Small Cleaved Cell Lymphoma", "shortest_name_length": 45}
{"curie": "UMLS:C4331335", "names": ["Stage IV Oropharyngeal (p16-Negative) Throat Cancer", "Stage IV Oropharyngeal (p16-Negative) Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Oropharyngeal (p16-Negative) Carcinoma AJCC v8", "shortest_name_length": 51}
{"curie": "MONDO:0019593", "names": ["46,XX DSD induced by fetal androgens excess", "46,XX disorder of sex development induced by fetal androgens excess"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XX disorder of sex development induced by fetal androgens excess", "shortest_name_length": 43}
{"curie": "UMLS:C3273228", "names": ["Lymph Node Follicular Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymph Node Follicular Hyperplasia", "shortest_name_length": 33}
{"curie": "MONDO:0001867", "names": ["Phaeomycosis", "Phaehyphomycosis", "Pheohyphomycosis", "phaehyphomycosis", "pheohyphomycosis", "PHAEOHYPHOMYCOSIS", "phaeohyphomycosis", "Phaeohyphomycoses", "Phaeohyphomycosis", "Phaeohyphomycosis, NOS", "Phaeohyphomycosis (disorder)", "phaehyphomycosis (diagnosis)", "Dematiaceous fungal infection", "infection by dematiacious fungi", "Infection by dematiaceous fungi", "Infection by dematiacious fungi", "Infection by dematiaceous fungi, NOS", "Infection by dematiacious fungi (Phaehyphomycosis)", "infection by dematiacious fungi [Phaehyphomycosis]", "Infection by dematiacious fungi [Phaehyphomycosis]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phaeohyphomycosis", "shortest_name_length": 12}
{"curie": "MONDO:0060583", "names": ["IMD71", "PLTEID", "immunodeficiency 71", "IMMUNODEFICIENCY 71 WITH INFLAMMATORY DISEASE AND CONGENITAL THROMBOCYTOPENIA", "immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia", "platelet abnormalities with eosinophilia and immune-mediated inflammatory disease", "PLATELET ABNORMALITIES WITH EOSINOPHILIA AND IMMUNE-MEDIATED INFLAMMATORY DISEASE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "platelet abnormalities with eosinophilia and immune-mediated inflammatory disease", "shortest_name_length": 5}
{"curie": "MONDO:0003206", "names": ["HEMANGIOMA AQUIRED", "HAEMANGIOMA AQUIRED", "Acquired hemangioma", "Acquired Hemangioma", "acquired hemangioma", "Hemangioma acquired", "Acquired haemangioma", "Haemangioma acquired"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired hemangioma", "shortest_name_length": 18}
{"curie": "UMLS:C1561251", "names": ["necrosis soft tissue neck", "Neck soft tissue necrosis", "necrosis of soft tissue of neck", "Neck Soft Tissue Necrotic Lesion", "necrosis of soft tissue of neck (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neck soft tissue necrosis", "shortest_name_length": 25}
{"curie": "UMLS:C4745249", "names": ["t(6;11) Renal Cell Carcinoma", "TFEB-Rearranged Renal Cell Carcinoma", "t(6;11);(p21;q12) Renal Cell Carcinoma", "Renal Cell Carcinoma with t(6;11);(p21;q12); MALAT1-TFEB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "TFEB-Rearranged Renal Cell Carcinoma", "shortest_name_length": 28}
{"curie": "UMLS:C4721433", "names": ["Stage IV Hypopharyngeal Epidermoid Carcinoma", "Stage IV Epidermoid Carcinoma of Hypopharynx", "Stage IV Squamous Cell Carcinoma of Hypopharynx", "Stage IV Hypopharyngeal Squamous Cell Carcinoma", "Stage IV Epidermoid Carcinoma of the Hypopharynx", "Stage IV Squamous Cell Carcinoma of the Hypopharynx", "Stage IV Hypopharyngeal Throat Squamous Cell Cancer", "Stage IV Hypopharyngeal Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Hypopharyngeal Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 44}
{"curie": "UMLS:C0472762", "names": ["ALPHA-THALASSEMIA TRAIT", "Alpha trait thalassemia", "THALASSEMIA ALPHA TRAIT", "alpha-thalassemia trait", "Alpha Thalassemia Trait", "Alpha thalassemia trait", "Alpha trait thalassaemia", "alpha Thalassemia, trait", "Alpha thalassaemia trait", "Alpha trait thalassemia (disorder)", "alpha-thalassemia trait (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alpha trait thalassemia", "shortest_name_length": 23}
{"curie": "UMLS:C1336325", "names": ["Stage II Testicular Nonseminomatous Germ Cell Tumor", "Stage II Testicular Non-Seminomatous Germ Cell Tumor", "Stage II Testicular Non-Seminomatous Germ Cell Tumor AJCC v7", "Stage II Testicular Non-Seminomatous Germ Cell Tumor AJCC v6", "Stage II Testicular Non-Seminomatous Germ Cell Tumor AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Testicular Non-Seminomatous Germ Cell Tumor AJCC v6 and v7", "shortest_name_length": 51}
{"curie": "UMLS:C5401376", "names": ["High Grade Anal Squamous Dysplasia", "High Grade Anal Intraepithelial Neoplasia", "High Grade Anal Squamous Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Anal Intraepithelial Neoplasia", "shortest_name_length": 34}
{"curie": "MONDO:0015339", "names": ["AMN", "ADRENOMYELONEUROPATHY", "adrenomyeloneuropathy", "Adrenomyeloneuropathy", "adrenomyeloneuropathy (AMN)", "adrenomyeloneuropathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adrenomyeloneuropathy", "shortest_name_length": 3}
{"curie": "MONDO:0011456", "names": ["NPH3", "Nph3", "NPHP3", "Nephronophthisis 3", "nephronophthisis 3", "NEPHRONOPHTHISIS 3", "nephronophthisis type 3", "Adolescent nephronophthisis", "Nephronophthisis, Adolescent", "NPHP3 nephronophthisis (disease)", "Adolescent nephronophthisis (disorder)", "nephronophthisis (disease) caused by mutation in NPHP3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephronophthisis 3", "shortest_name_length": 4}
{"curie": "MONDO:0013942", "names": ["CGD", "CG9", "PBD8A", "peroxisome biogenesis disorder 8A", "Peroxisome Biogenesis Disorder 8A", "peroxisome biogenesis disorder 8A (Zellweger)", "PEROXISOME BIOGENESIS DISORDER 8A (ZELLWEGER)", "Peroxisome Biogenesis Disorder, Complementation Group D", "peroxisome biogenesis disorder, complementation group 9", "peroxisome biogenesis disorder, complementation group D", "PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP D", "PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 9", "Peroxisome Biogenesis Disorder, Complementation Group 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder 8A (Zellweger)", "shortest_name_length": 3}
{"curie": "MONDO:0014867", "names": ["SCA43", "SPINOCEREBELLAR ATAXIA 43", "spinocerebellar ataxia 43", "cerebellar ataxia type 43", "spinocerebellar ataxia type 43", "Spinocerebellar ataxia type 43", "spinocerebellar ataxia 43; SCA43", "MME autosomal dominant cerebellar ataxia", "Spinocerebellar ataxia type 43 (disorder)", "autosomal dominant cerebellar ataxia caused by mutation in MME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia 43", "shortest_name_length": 5}
{"curie": "UMLS:C5420861", "names": ["Unresectable Thyroid Gland Follicular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Thyroid Gland Follicular Carcinoma", "shortest_name_length": 47}
{"curie": "MONDO:0021080", "names": ["Vascular Tumor", "vascular tumor", "Vascular Tumors", "vascular tumors", "tumors, vascular", "Tumors, Vascular", "Vascular Neoplasm", "Vascular neoplasm", "vascular neoplasm", "Vascular Neoplasms", "tumor blood vessel", "neoplasms vascular", "vascular neoplasms", "blood tumor vessel", "blood vessel tumor", "Blood Vessel Tumor", "Neoplasm, Vascular", "Blood vessel tumor", "Vascular neoplasms", "Blood vessel tumour", "Blood Vessel Tumors", "BLOOD VESSEL TUMORS", "Neoplasms, Vascular", "blood vessel tumors", "neoplasms, vascular", "Tumor, Blood Vessel", "Tumors, Blood Vessel", "blood tumors vessels", "Blood Vessel Neoplasm", "vascular tissue tumor", "Vascular Tissue Tumor", "Blood vessel neoplasm", "tumor of blood vessel", "blood vessel neoplasm", "Blood-vessels--Tumors", "tumor of vascular tissue", "vascular tissue neoplasm", "Vascular Tissue Neoplasm", "neoplasm of blood vessel", "Neoplasm of blood vessel", "Tumor of Vascular Tissue", "Vascular Tissue Neoplasms", "Neoplasm, Vascular Tissue", "Neoplasms, Vascular Tissue", "Neoplasm of Vascular Tissue", "neoplasm of vascular tissue", "Blood vessel tumor disorder", "Blood vessel tumour disorder", "blood vessel neoplasm (disease)", "Neoplasm of blood vessel (disorder)", "neoplasm of blood vessel (diagnosis)", "Blood vessel tumor (morphologic abnormality)", "Blood vessel neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blood vessel neoplasm", "shortest_name_length": 14}
{"curie": "MONDO:0016617", "names": ["rheumatoid factor-negative JIA with anti-nuclear antibodies", "polyarthritis without rheumatoid factor with anti-nuclear antibodies", "juvenile rheumatoid factor-negative polyarthritis with anti-nuclear antibodies", "rheumatoid factor-negative juvenile idiopathic arthritis with anti-nuclear antibodies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rheumatoid factor-negative juvenile idiopathic arthritis with anti-nuclear antibodies", "shortest_name_length": 59}
{"curie": "UMLS:C0234935", "names": ["Acute urticaria", "acute urticaria", "URTICARIA ACUTE", "Urticaria acute", "Acute urticaria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute urticaria", "shortest_name_length": 15}
{"curie": "UMLS:C5206444", "names": ["Stage IIA Cervical Cancer FIGO 2018", "Stage IIA Cervical Carcinoma FIGO 2018"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Cervical Cancer FIGO 2018", "shortest_name_length": 35}
{"curie": "MONDO:0004382", "names": ["Larynx", "larynx disease", "Larynx Disease", "disease larynx", "Larynx Diseases", "diseases larynx", "larynx disorder", "larynx; disease", "larynx diseases", "Disease, Larynx", "Larynx--Diseases", "disorders larynx", "Diseases, Larynx", "Disease of larynx", "disease of larynx", "Laryngeal Disease", "laryngeal disease", "laryngeal disorder", "Disease, Laryngeal", "Laryngeal Disorder", "laryngeal diseases", "Laryngeal Diseases", "Laryngeal disorder", "disorder of larynx", "Disorder of larynx", "Diseases, Laryngeal", "Laryngeal Disorders", "laryngeal disorders", "disease of the larynx", "Disease of larynx NOS", "disorder of the larynx", "DISEASES OF THE LARYNX", "Disorder of the larynx", "Laryngeal disorder NOS", "Disease of the larynx, NOS", "larynx disease or disorder", "Disease or syndrome of larynx", "disease (or disorder); larynx", "Unspecified disease of larynx", "disease or disorder of larynx", "disorder of larynx (diagnosis)", "Disorder of the larynx (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laryngeal disorder", "shortest_name_length": 6}
{"curie": "UMLS:C5419081", "names": ["Unresectable Bile Duct Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Bile Duct Carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0017218", "names": ["Septopreoptic HPE", "septopreoptic holoprosencephaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "septopreoptic holoprosencephaly", "shortest_name_length": 17}
{"curie": "UMLS:C2348655", "names": ["TdT Negative Acute Lymphoblastic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "TdT Negative Acute Lymphoblastic Leukemia", "shortest_name_length": 41}
{"curie": "UMLS:C1711308", "names": ["Benign Accessory Urethral Gland Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Accessory Urethral Gland Neoplasm", "shortest_name_length": 40}
{"curie": "UMLS:C5204477", "names": ["Borderline Ovarian Endometrioid Tumor/Atypical Proliferative Ovarian Endometrioid Tumor with Microinvasion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Ovarian Endometrioid Tumor/Atypical Proliferative Ovarian Endometrioid Tumor with Microinvasion", "shortest_name_length": 106}
{"curie": "MONDO:0007483", "names": ["RAD", "DSH", "DSH1", "Acropigmentation of Dohi", "acropigmentation of Dohi", "RETICULATE ACROPIGMENTATION OF DOHI", "reticulate acropigmentation of Dohi", "Reticulate acropigmentation of Dohi", "Reticulate Acropigmentation of Dohi", "Dyschromatosis symmetrica hereditaria", "DYSCHROMATOSIS SYMMETRICA HEREDITARIA", "dyschromatosis symmetrica hereditaria", "Dyschromatosis Symmetrica Hereditaria", "dyschromatosis symmetrica hereditaria 1", "Dyschromatosis symmetrica hereditaria 1", "Dyschromatosis Symmetrica Hereditaria 1", "DYSCHROMATOSIS SYMMETRICA HEREDITARIA 1", "Symmetrical dyschromatosis of extremities", "symmetric dyschromatosis of the extremities", "Symmetric dyschromatosis of the extremities", "SYMMETRIC DYSCHROMATOSIS OF THE EXTREMITIES", "Symmetric Dyschromatosis of the Extremities", "Familial reticulate acropigmentation of Dohi", "familial reticulate acropigmentation of Dohi", "Symmetrical dyschromatosis of extremities (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyschromatosis symmetrica hereditaria", "shortest_name_length": 3}
{"curie": "MONDO:0003021", "names": ["CNS angiosarcoma", "CNS Angiosarcoma", "CNS hemangiosarcoma", "angiosarcoma of CNS", "CNS Hemangiosarcoma", "Angiosarcoma of CNS", "hemangiosarcoma of CNS", "Hemangiosarcoma of CNS", "Angiosarcoma of the CNS", "angiosarcoma of the CNS", "Hemangiosarcoma of the CNS", "hemangiosarcoma of the CNS", "central nervous system angiosarcoma", "Central Nervous System Angiosarcoma", "Central Nervous System Hemangiosarcoma", "Angiosarcoma of Central Nervous System", "angiosarcoma of central nervous system", "central nervous system hemangiosarcoma", "Hemangiosarcoma of Central Nervous System", "hemangiosarcoma of central nervous system", "angiosarcoma of the central nervous system", "Angiosarcoma of the Central Nervous System", "hemangiosarcoma of the central nervous system", "central nervous system angiosarcoma (disease)", "Hemangiosarcoma of the Central Nervous System", "angiosarcoma (disease) of central nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system angiosarcoma", "shortest_name_length": 16}
{"curie": "UMLS:C4683235", "names": ["Clinical Stage IV Retinoblastoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage IV Retinoblastoma AJCC v8", "shortest_name_length": 40}
{"curie": "UMLS:C4288012", "names": ["Vulvar Adenocarcinoma of Sweat Gland Type", "Vulvar Adenocarcinoma of Sweat Gland Origin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Adenocarcinoma of Sweat Gland Origin", "shortest_name_length": 41}
{"curie": "MONDO:0000478", "names": ["multifocal dystonia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multifocal dystonia", "shortest_name_length": 19}
{"curie": "MONDO:0010321", "names": ["AUTSX1", "autism susceptibility, X-linked 1", "susceptibility to X-linked autism 1", "AUTISM, SUSCEPTIBILITY TO, X-LINKED 1", "autism, susceptibility to, X-linked 1", "autism, susceptibility to, X-linked type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autism, susceptibility to, X-linked 1", "shortest_name_length": 6}
{"curie": "MONDO:0010704", "names": ["OPD1", "Taybi", "OPD syndrome", "OPD syndrome 1", "OPD SYNDROME 1", "OPD I SYNDROME", "Taybi syndrome", "syndrome taybi", "OPD I syndrome", "taybi syndrome", "OPD 1 syndrome", "Taybi's syndrome", "Opd Syndrome, Type 1", "otopalatodigital syndrome I", "Oto-palatal-digital syndrome", "oto palatal digital syndrome", "syndrome; oto-palatal-digital", "oto-palatal-digital; syndrome", "otopalatodigital syndrome type I", "otopalatodigital syndrome type 1", "Otopalatodigital syndrome type 1", "Otopalatodigital Syndrome Type 1", "otopalatodigital syndrome, type I", "Otopalatodigital Syndrome, Type I", "otopalatodigital syndrome, type 1", "otopalatodigital (OPD) syndrome I", "OTOPALATODIGITAL SYNDROME, TYPE I", "Otopalatodigital syndrome, type 1", "oto-palato-digital syndrome type 1", "Oto-Palato-digital syndrome type 1", "otopalatodigital spectrum disorder", "Oto-palato-digital syndrome, type I", "frontootopalatodigital osteodysplasia", "FRONTOOTOPALATODIGITAL OSTEODYSPLASIA", "Frontootopalatodigital Osteodysplasia", "oto-palato-digital syndrome type 1 (diagnosis)", "Oto-palato-digital syndrome, type I (disorder)", "otopalatodigital syndrome, type I, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "otopalatodigital syndrome type 1", "shortest_name_length": 4}
{"curie": "UMLS:C1333173", "names": ["PCHL", "Primary Cutaneous Hodgkin Disease", "Primary Cutaneous Hodgkin Lymphoma", "Primary Cutaneous Hodgkin's Disease", "Primary Cutaneous Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Cutaneous Hodgkin Lymphoma", "shortest_name_length": 4}
{"curie": "MONDO:0020680", "names": ["Capillary pneumonia", "Acute bronchiolitis", "bronchiolitis acute", "Bronchiolitis;acute", "acute Bronchiolitis", "Acute Bronchiolitis", "acute bronchiolitis", "capillary pneumonia", "acute; bronchiolitis", "bronchiolitis; acute", "Bronchiolitis (acute)", "Acute bronchiolitis, NOS", "Acute capillary bronchiolitis", "acute capillary bronchiolitis", "Acute bronchiolitis (disorder)", "Acute bronchiolitis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute bronchiolitis", "shortest_name_length": 19}
{"curie": "MONDO:0018141", "names": ["pyruvate carboxylase deficiency type A", "pyruvate carboxylase deficiency, infantile form", "pyruvate carboxylase deficiency, infantile type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyruvate carboxylase deficiency, infantile form", "shortest_name_length": 38}
{"curie": "UMLS:C0269863", "names": ["First degree perineal tear", "First degree perineal laceration", "First Degree Perineal Laceration", "Obstetrical laceration, first degree", "First degree perineal laceration, NOS", "Laceration, obstetrical, first degree", "laceration; vulva, complicating delivery", "vulva; laceration, complicating delivery", "perineal rupture, obstetric; first degree", "First degree perineal tear during delivery", "First degree perineal laceration (disorder)", "First-degree perineal laceration during delivery", "first-degree perineal laceration during delivery", "First degree perineal laceration during delivery", "First degree perineal laceration (physical finding)", "rupture; perineum, complicating delivery, first degree", "Laceration of superficial layers of perineal structures", "laceration; vagina, complicating delivery, with perineum", "vagina; laceration, complicating delivery, with perineum", "post-delivery exam showing first degree perineal laceration", "first-degree perineal laceration during delivery (diagnosis)", "post-delivery exam showing first degree laceration of perineum", "post-delivery exam showing first degree laceration of perineum (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "First-degree perineal laceration during delivery", "shortest_name_length": 26}
{"curie": "UMLS:C4086444", "names": ["Hepatic Thrombosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatic Thrombosis", "shortest_name_length": 18}
{"curie": "MONDO:0012872", "names": ["THPH9", "thrombophilia due to decreased release of PLAT", "thrombophilia, familial, due to decreased release of PLAT", "hyperfibrinolysis, familial, due to increased release of plat", "thrombophilia, familial, due to decreased release of tissue plasminogen activator", "THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR", "Thrombophilia, Familial, Due To Decreased Release Of Tissue Plasminogen Activator", "hyperfibrinolysis, familial, due to increased release of tissue plasminogen activator", "HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR", "Hyperfibrinolysis, Familial, Due To Increased Release Of Tissue Plasminogen Activator"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombophilia, familial, due to decreased release of tissue plasminogen activator", "shortest_name_length": 5}
{"curie": "MONDO:0001521", "names": ["explosive disorder", "Explosive Disorder", "Explosive personality", "Explosive Personality", "explosive personality", "impulsive personality disorder", "explosive disorder (diagnosis)", "disorder explosive personality", "explosive personality disorder", "Explosive personality disorder", "Impulsive personality disorder", "explosive; personality disorder", "personality disorder; explosive", "intermittent explosive disorder", "explosive intermittent disorder", "Intermittent Explosive Disorder", "Intermittent explosive disorder", "intermittent explosive; disorder", "disorder; intermittent explosive", "Explosive personality (disorder)", "Explosive Disorder, Intermittent", "Intermittent Explosive Disorders", "Disorders, Intermittent Explosive", "Explosive personality disorder (disorder)", "explosive personality disorder (diagnosis)", "Intermittent explosive disorder (disorder)", "intermittent explosive disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intermittent explosive disorder", "shortest_name_length": 18}
{"curie": "MONDO:0000173", "names": ["muscular dystrophy-dystroglycanopathy, type C"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy-dystroglycanopathy, type C", "shortest_name_length": 45}
{"curie": "MONDO:0005512", "names": ["peritoneal mesothelioma", "malignant peritoneal mesothelioma", "malignant mesothelioma of peritoneum", "diffuse malignant peritoneal mesothelioma", "primary malignant peritoneal mesothelioma", "advanced malignant peritoneal mesothelioma", "Advanced Peritoneal Malignant Mesothelioma", "advanced peritoneal malignant mesothelioma", "Peritoneal mesothelioma malignant advanced", "peritoneum malignant mesothelioma (disease)", "Malignant Peritoneal Mesothelioma, Advanced", "malignant peritoneal mesothelioma, advanced", "peritoneal mesothelioma (disease), malignant", "Advanced malignant Mesothelioma of Peritoneum", "advanced malignant mesothelioma of peritoneum", "Advanced Malignant Mesothelioma of Peritoneum", "malignant mesothelioma (disease) of peritoneum", "advanced malignant mesothelioma of the peritoneum", "Advanced Malignant Mesothelioma of the Peritoneum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant peritoneal mesothelioma", "shortest_name_length": 23}
{"curie": "MONDO:0000384", "names": ["Benign Bladder Tumor", "bladder tumor benign", "BLADDER TUMOR BENIGN", "Benign bladder tumor", "benign bladder tumor", "benign bladder tumors", "Benign bladder tumour", "benign bladder tumours", "Benign Tumor of Bladder", "bladder benign neoplasm", "Benign Bladder Neoplasm", "benign bladder neoplasm", "Neoplasm benign;bladder", "benign tumor of bladder", "Benign Neoplasm of Bladder", "benign neoplasm of bladder", "Benign neoplasm of bladder", "Benign Tumor of the Bladder", "benign tumor of the bladder", "Benign bladder neoplasm NOS", "Benign Urinary Bladder Tumor", "benign urinary bladder tumor", "benign neoplasm of the bladder", "Benign Neoplasm of the Bladder", "benign tumor of urinary bladder", "benign urinary bladder neoplasm", "Benign tumor of urinary bladder", "urinary bladder benign neoplasm", "Benign neoplasm of bladder, NOS", "Benign Tumor of Urinary Bladder", "Benign Urinary Bladder Neoplasm", "Benign tumour of urinary bladder", "Benign Neoplasm of Urinary Bladder", "benign neoplasm of urinary bladder", "benign tumor of the urinary bladder", "Benign Tumor of the Urinary Bladder", "Benign neoplasm of bladder (disorder)", "Benign Neoplasm of the Urinary Bladder", "benign neoplasm of the urinary bladder", "benign neoplasm of bladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder benign neoplasm", "shortest_name_length": 20}
{"curie": "MONDO:0017169", "names": ["mea", "men", "MEN", "MEA", "meas", "MEA SYNDROME", "men syndrome", "MEN syndrome", "MEN syndromes", "men syndromes", "MEN Syndromes", "Endocrine adenomatosis", "multiple endocrine adenoma", "multiple endocrine tumasia", "Multiple endocrine tumasia", "multiple endocrine neoplasm", "Multiple endocrine adenomas", "Multiple Endocrine Neoplasms", "endocrine multiple neoplasia", "Multiple Endocrine Neoplasia", "multiple endocrine neoplasia", "multiple endocrine neoplasms", "Multiple polyglandular tumor", "Multiple endocrine neoplasia", "Multiple Endocrine Adenopathy", "Endocrine Neoplasms, Multiple", "multiple endocrine neoplasias", "Neoplasms, Multiple Endocrine", "multiple endocrine adenopathy", "Multiple endocrine neoplasias", "Neoplasia, Multiple Endocrine", "Endocrine Neoplasia, Multiple", "Adenopathy, Multiple Endocrine", "Endocrine Adenopathy, Multiple", "Multiple Endocrine Adenopathies", "multiple endocrine adenomatosis", "Familial Endocrine Adenomatosis", "Familial Endocrine Adenomatoses", "Multiple Endocrine Adenomatoses", "Multiple endocrine adenomatosis", "Multiple Endocrine Adenomatosis", "Adenomatosis, Familial endocrine", "Endocrine Adenomatosis, Familial", "Adenomatosis, Multiple Endocrine", "Endocrine Adenomatosis, Multiple", "Endocrine Adenomatoses, Familial", "Adenomatoses, Multiple Endocrine", "Endocrine Adenomatoses, Multiple", "Adenomatosis, Familial Endocrine", "Endocrine Adenopathies, Multiple", "Adenomatoses, Familial Endocrine", "Adenopathies, Multiple Endocrine", "MEN - Multiple endocrine neoplasia", "Multiple Endocrine Adenomatosis NOS", "Multiple endocrine adenomatosis NOS", "Familial polyendocrine adenomatosis", "MEA - Multiple endocrine adenomatosis", "Multiple endocrine neoplasia syndrome", "Multiple Endocrine Neoplasia Syndrome", "multiple endocrine neoplasia syndrome", "Multiple Endocrine Neoplasia Syndromes", "Multiple endocrine neoplasia syndromes", "multiple endocrine neoplasia syndrome(s)", "multiple endocrine neoplasia (diagnosis)", "Multiple Endocrine Neoplasia Syndrome(s)", "Multiple endocrine adenomatosis syndrome", "Multiple endocrine neoplasia [MEN] syndromes", "Multiple endocrine neoplasia [MEN] syndrome NOS", "Multiple endocrine adenomas (morphologic abnormality)", "Multiple endocrine neoplasia [MEN] syndrome, unspecified", "Polyglandular activity in multiple endocrine adenomatosis", "Polyglandular activity in multiple endocrine adenomatosis (disorder)", "Polyglandular activity in multiple endocrine adenomatosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple endocrine neoplasia", "shortest_name_length": 3}
{"curie": "MONDO:0017869", "names": ["chondroectodermal dysplasia with night blindness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chondroectodermal dysplasia with night blindness", "shortest_name_length": 48}
{"curie": "MONDO:0007972", "names": ["Ménière", "aural vertigo", "Aural Vertigo", "Aural vertigo", "Vertigo;aural", "vertigo; aural", "Vertigo, Aural", "aural; vertigo", "meniere disease", "MENIERE DISEASE", "Meniere Disease", "Mnire's vertigo", "Ménière Disease", "Meniere disease", "Meniere disorder", "Disease, Meniere", "Menieres Disease", "Ménière Diseases", "Disease, Ménière", "Meniere syndrome", "Ménières Disease", "Menieres disease", "Meniere Syndrome", "Otogenic Vertigo", "otogenic vertigo", "Disease;Menieres", "meniere syndrome", "Auditory Vertigo", "Otogenic vertigo", "Auditory vertigo", "MENIERES DISEASE", "Vertigo;otogenic", "vertigo; auditory", "MENIERE'S DISEASE", "Ménière's disease", "vertigo; otogenic", "meniere's disease", "Meniere's Disease", "Meniere's disease", "Ménière's vertigo", "otogenic; vertigo", "Vertigo, Auditory", "Diseases, Ménière", "Auditory Vertigos", "auditory; vertigo", "Otogenic Vertigos", "Vertigo, Otogenic", "Menieres Syndrome", "Ménière's Disease", "Vertigos, Otogenic", "Ménière's Diseases", "Vertigos, Auditory", "Disease, Ménière's", "Disease, Meniere's", "labyrinth; hydrops", "MENIERE'S SYNDROME", "Meniere's syndrome", "Syndrome Meniere's", "hydrops; labyrinth", "Ménière's syndrome", "Meniere's Syndrome", "SYNDROME MENIERE'S", "meniere's syndrome", "Diseases, Ménière's", "Syndrome, Meniere's", "Meniere's disease, NOS", "Meniere's vertigo, NOS", "Meniere's syndrome, NOS", "aural vertigo (symptom)", "aural vertigo (diagnosis)", "otogenic vertigo (diagnosis)", "Ménière's disease (disorder)", "Meniere's disease (diagnosis)", "Meniere's syndrome or vertigo", "Ménière's syndrome or vertigo", "Ménière's disease, unspecified", "Meniere's disease, unspecified", "Idiopathic Endolymphatic Hydrops", "spinning dizziness caused by noise", "Ménière's disease, unspecified ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meniere disease", "shortest_name_length": 7}
{"curie": "UMLS:C2910118", "names": ["Congenital atresia or stricture of osseous meatus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital atresia or stricture of osseous meatus", "shortest_name_length": 49}
{"curie": "UMLS:C4725594", "names": ["Thoracic Esophagus Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thoracic Esophagus Adenocarcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C1332432", "names": ["BMT Nephropathy", "Bone Marrow Transplantation Nephropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone Marrow Transplantation Nephropathy", "shortest_name_length": 15}
{"curie": "UMLS:C0677726", "names": ["Recurrent Aggressive Non-Hodgkin Lymphoma", "Recurrent Aggressive Adult Non-Hodgkin Lymphoma", "recurrent aggressive adult non-Hodgkin lymphoma", "aggressive, recurrent adult non-Hodgkin lymphoma", "recurrent aggressive adult non-Hodgkin's lymphoma", "Recurrent Aggressive Adult Non-Hodgkin's Lymphoma", "Recurrent Adult Aggressive Non-Hodgkin's Lymphoma", "Aggressive Recurrent Adult Non-Hodgkin's Lymphoma", "recurrent adult aggressive non-Hodgkin's lymphoma", "aggressive recurrent adult non-Hodgkin's lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Aggressive Adult Non-Hodgkin Lymphoma", "shortest_name_length": 41}
{"curie": "MONDO:0002290", "names": ["Clitoral Ca", "clitoral Ca", "clitoral cancer", "clitoris cancer", "Cancer of clitoris", "cancer of clitoris", "carcinoma of Clitoris", "carcinoma of clitoris", "Malignant Clitoris Tumor", "Malignant Clitoral Tumor", "malignant clitoral tumor", "malignant clitoris tumor", "Malignant Tumor of Clitoris", "malignant clitoris neoplasm", "malignant tumor of clitoris", "Malignant Clitoris Neoplasm", "malignant clitoral neoplasm", "malignant tumor of Clitoris", "Malignant Clitoral Neoplasm", "Malignant Neoplasm of Clitoris", "malignant neoplasm of clitoris", "Malignant neoplasm of clitoris", "Malignant Tumor of the Clitoris", "malignant tumor of the clitoris", "malignant neoplasm of the clitoris", "Malignant Neoplasm of the Clitoris", "Primary malignant neoplasm of clitoris", "Malignant neoplasm of clitoris (disorder)", "vulvar neoplasm malignant clitoris primary", "malignant neoplasm of clitoris (diagnosis)", "Primary malignant neoplasm of clitoris (disorder)", "Primary malignant neoplasm of clitoris (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "clitoris cancer", "shortest_name_length": 11}
{"curie": "MONDO:0012814", "names": ["Diastasis Recti And Weakness Of The Linea Alba", "DIASTASIS RECTI AND WEAKNESS OF THE LINEA ALBA", "diastasis recti and weakness of the linea alba"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diastasis recti and weakness of the linea alba", "shortest_name_length": 46}
{"curie": "MONDO:0014324", "names": ["PC3", "pachyonychia congenita 3", "PACHYONYCHIA CONGENITA 3", "KRT6A pachyonychia congenita", "pachyonychia congenita type 3", "pachyonychia congenita caused by mutation in KRT6A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pachyonychia congenita 3", "shortest_name_length": 3}
{"curie": "MONDO:0032751", "names": ["DA2B3", "distal arthrogryposis type 2B3", "ARTHROGRYPOSIS, DISTAL, TYPE 2B3", "arthrogryposis, distal, type 2B3", "distal arthrogryposis type 2B3 (Sheldon-Hall)", "arthrogryposis, distal, type 2B3 (Sheldon-Hall)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis, distal, type 2B3", "shortest_name_length": 5}
{"curie": "MONDO:0002798", "names": ["Childhood CNS PNET", "childhood CNS PNET", "Pediatric CNS PNET", "pediatric CNS PNET", "childhood central nervous system PNET", "Childhood Central Nervous System PNET", "Central nervous system embryonal tumor, NOS", "Central Nervous System Embryonal Tumor, NOS", "pediatric CNS primitive neuroectodermal tumor", "Pediatric CNS Primitive Neuroectodermal Tumor", "Childhood CNS Primitive Neuroectodermal Tumor", "childhood CNS primitive neuroectodermal tumor", "childhood CNS primitive neuroectodermal neoplasm", "Pediatric CNS Primitive Neuroectodermal Neoplasm", "childhood central nervous system embryonal tumor", "pediatric CNS primitive neuroectodermal neoplasm", "Childhood CNS Primitive Neuroectodermal Neoplasm", "Childhood Central Primitive Neuroectodermal Tumor", "pediatric central primitive neuroectodermal tumor", "Pediatric Central Primitive Neuroectodermal Tumor", "childhood central primitive neuroectodermal tumor", "childhood central primitive neuroectodermal neoplasm", "pediatric central primitive neuroectodermal neoplasm", "Childhood Central Primitive Neuroectodermal Neoplasm", "Pediatric Central Primitive Neuroectodermal Neoplasm", "Childhood Central Nervous System Embryonal Tumor, NOS", "Pediatric Central Nervous System Primitive Neuroectodermal Tumor", "childhood central nervous system primitive neuroectodermal tumor", "Childhood Central Nervous System Primitive Neuroectodermal Tumor", "pediatric central nervous system primitive neuroectodermal tumor", "Pediatric Central Nervous System Primitive Neuroectodermal Neoplasm", "Childhood Central Nervous System Primitive Neuroectodermal Neoplasm", "childhood central nervous system primitive neuroectodermal neoplasm", "pediatric central nervous system primitive neuroectodermal neoplasm", "central nervous system primitive neuroectodermal neoplasm of childhood", "Childhood Central Nervous System Embryonal Tumor, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood central nervous system primitive neuroectodermal neoplasm", "shortest_name_length": 18}
{"curie": "UMLS:C1527258", "names": ["Infantile Paralysis", "INFANTILE PARALYSIS", "infantile paralysis", "Infantile paralysis", "infantile; paralysis", "paralysis; infantile", "Paralysis, Infantile", "Paralysis (Infantile)", "Infantile paralysis, NOS", "Infantile paralytic paralysis", "Infantile paralysis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infantile paralysis", "shortest_name_length": 19}
{"curie": "MONDO:0019579", "names": ["discrete papular lichen myxedematosus", "Discrete papular lichen myxedematosus", "Discrete papular lichen myxoedematosus", "Discrete papular lichen myxedematosus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "discrete papular lichen myxedematosus", "shortest_name_length": 37}
{"curie": "MONDO:0009783", "names": ["arPEO", "PEOB1", "autosomal recessive progressive external ophthalmoplegia", "autosomal recessive progressive external ophthalmoplegia 1", "PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE 1", "progressive external ophthalmoplegia, autosomal recessive 1", "POLG autosomal recessive progressive external ophthalmoplegia", "progressive external ophthalmoplegia with cerebellar ataxia infantile", "cerebellar ataxia infantile with progressive external ophthalmoplegia", "autosomal recessive progressive external ophthalmoplegia caused by mutation in POLG", "PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 1", "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 1", "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 1", "shortest_name_length": 5}
{"curie": "UMLS:C0270764", "names": ["LMN disease", "Lower motor neuron disease", "Lower Motor Neuron Disease", "Motor Neuron Disease, Lower", "Lower motor neuron disease, NOS", "Lower motor neuron disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Motor Neuron Disease, Lower", "shortest_name_length": 11}
{"curie": "UMLS:C0018614", "names": ["Hashish Abuse", "hashish; abuse", "Abuse, Hashish", "abuse; hashish"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hashish Abuse", "shortest_name_length": 13}
{"curie": "MONDO:0007502", "names": ["PHEP", "Posterior helical pits", "POSTERIOR HELICAL EAR PITS", "posterior helical Ear pits", "ear pits, posterior helical", "EAR PITS, POSTERIOR HELICAL", "earlobe Indentations, posterior", "EARLOBE INDENTATIONS, POSTERIOR"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ear pits, posterior helical", "shortest_name_length": 4}
{"curie": "MONDO:0043885", "names": ["Eye infection", "eye infection", "Infection;eye", "EYE INFECTION", "infection eye", "Eye Infection", "infection; eye", "Infection, Eye", "eye infections", "Eye Infections", "eyes infection", "eye; infection", "infection, eye", "eyes infections", "infections, eye", "Infections, Eye", "Eye--Infections", "ocular infection", "Ocular Infection", "Ocular infections", "Ocular Infections", "infection, ocular", "ocular infections", "Eye infection NOS", "Infection, Ocular", "infections, ocular", "Infections, Ocular", "eye infectious disorder", "Eye infection (disorder)", "Eye infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eye infectious disorder", "shortest_name_length": 13}
{"curie": "UMLS:C0153678", "names": ["Pleural seedling", "Pleural metastases", "Metastasis to pleura", "Metastases to Pleura", "Metastases to pleura", "Metastasis to the Pleura", "Cancer metastatic to pleura", "Metastatic Tumor to the Pleura", "Metastatic Neoplasm to the Pleura", "Secondary malignant tumor of pleura", "Secondary malignant tumour of pleura", "secondary malignant neoplasm of pleura", "Secondary malignant neoplasm of pleura", "Metastatic malignant neoplasm to pleura", "Metastatic malignant neoplasm of pleura", "Malignant neoplasm of pleura metastatic", "Secondary malignant neoplasm of pleura, NOS", "Metastatic Malignant Neoplasm to the Pleura", "Metastatic Malignant Neoplasm in the Pleura", "Metastatic malignant neoplasm to pleura, NOS", "secondary malignant neoplasm of pleura (diagnosis)", "Metastatic malignant neoplasm to pleura (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to pleura", "shortest_name_length": 16}
{"curie": "MONDO:0023809", "names": ["Milner Khallouf Gibson syndrome", "Milner-Khallouf-Gibson syndrome", "microcephaly, short stature, slow growth, beak nose, micrognathia, skin dyspigmentation and forearm and thumb dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Milner-Khallouf-Gibson syndrome", "shortest_name_length": 31}
{"curie": "MONDO:0018357", "names": ["neonatal Hughes syndrome", "neonatal antiphospholipid syndrome", "neonatal antiphospholipid antibody syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal antiphospholipid syndrome", "shortest_name_length": 24}
{"curie": "MONDO:0006693", "names": ["cerebral artery disease", "Cerebral Artery Disease", "Cerebral Artery Diseases", "Artery Disease, Cerebral", "Disease, Cerebral Artery", "Artery Diseases, Cerebral", "Diseases, Cerebral Artery", "cerebral arterial disease", "Cerebral Arterial Disease", "Arterial Disease, Cerebral", "Disease, Cerebral Arterial", "artery; disorder, cerebral", "Cerebral Arterial Diseases", "Diseases, Cerebral Arterial", "Arterial Diseases, Cerebral", "cerebral; disorder arterial, artery", "disease (or disorder); artery, cerebral", "disease (or disorder); cerebral, arterial, artery"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral arterial disease", "shortest_name_length": 23}
{"curie": "MONDO:0010185", "names": ["MAHCD", "cblD defect", "CblD defect", "Cobalamin D defect", "cobalamin D defect", "cobalamin D disease", "Cobalamin D disease", "cobalamin d disease", "Cobalamin D deficiency", "cobalamin D deficiency", "cblD - cobalamin locus d", "CblD - Cobalamin locus D", "Cobalamin D disease (disorder)", "cobalamin D disease (diagnosis)", "m0e.321 cobalamin locus d variant", "methylmalonic acidemia, Cblh type", "methylmalonic aciduria, Cblh type", "M0E.321 Cobalamin locus D variant", "HOMOCYSTINURIA, cblD TYPE, VARIANT 1", "Homocystinuria, CblD Type, Variant 1", "homocystinuria, cblD type, variant 1", "methylmalonic aciduria, Cblh type, formerly", "methylmalonic acidemia, Cblh type, formerly", "METHYLMALONIC ACIDURIA, cblH TYPE, FORMERLY", "METHYLMALONIC ACIDEMIA, cblH TYPE, FORMERLY", "methylmalonic aciduria, cblD type, variant 2", "Methylmalonic Aciduria, CblD Type, Variant 2", "METHYLMALONIC ACIDURIA, cblD TYPE, VARIANT 2", "homocystinuria, cblD type, variant 1, included", "CblD methylmalonic acidemia and homocystinuria", "cblD methylmalonic acidemia and homocystinuria", "CblD methylmalonic acidaemia and homocystinuria", "Mehtylmalonic acidemia with homocystinuria cbI d", "methylmalonic aciduria and homocystinuria type cblD", "methylmalonic acidemia and homocystinuria, cblD type", "methylmalonic acidemia with homocystinuria type cblD", "Methylmalonic Acidemia and Homocystinuria, CblD Type", "Methylmalonic Aciduria and Homocystinuria, CblD Type", "METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblD TYPE", "Methylmalonic Aciduria and Homocystinuria, cblD Type", "METHYLMALONIC ACIDEMIA AND HOMOCYSTINURIA, cblD TYPE", "methylmalonic aciduria and homocystinuria, cblD type", "Methylmalonic aciduria with homocystinuria, type cblD", "methylmalonic aciduria with homocystinuria, type cblD", "methylmalonic acidemia with homocystinuria, type cblD", "Methylmalonic acidemia with homocystinuria, type cblD", "methylmalonic aciduria, cblD type, variant 2, included", "combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblD", "Combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblD"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "methylmalonic aciduria and homocystinuria type cblD", "shortest_name_length": 5}
{"curie": "MONDO:0100502", "names": ["NTHL1-deficiency tumor predisposition syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "NTHL1-deficiency tumor predisposition syndrome", "shortest_name_length": 46}
{"curie": "UMLS:C5446440", "names": ["Metastatic Malignant Neoplasm in the Lacrimal Drainage System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Malignant Neoplasm in the Lacrimal Drainage System", "shortest_name_length": 61}
{"curie": "MONDO:0011530", "names": ["mesomelic dysplasia Savarirayan type", "Mesomelic dysplasia Savarirayan type", "triangular tibia and fibular aplasia", "MESOMELIC DYSPLASIA, SAVARIRAYAN TYPE", "Mesomelic Dysplasia, Savarirayan Type", "Mesomelic dysplasia, Savarirayan type", "mesomelic dysplasia, Savarirayan type", "triangular tibia-fibular aplasia syndrome", "Triangular tibia-fibular aplasia syndrome", "Mesomelic dysplasia Savarirayan type (disorder)", "Mesomelic dysplasia with absent fibula and triangular tibia", "Mesomelic Dysplasia with Absent Fibulas and Triangular Tibias", "MESOMELIC DYSPLASIA WITH ABSENT FIBULAS AND TRIANGULAR TIBIAS", "mesomelic dysplasia with absent fibulas and triangular tibias", "Mesomelic dysplasia with absent fibulas and triangular tibias"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mesomelic dysplasia, Savarirayan type", "shortest_name_length": 36}
{"curie": "UMLS:C1335517", "names": ["Prostate Non-Neoplastic Disease", "Prostate Non-Neoplastic Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Non-Neoplastic Disorder", "shortest_name_length": 31}
{"curie": "MONDO:0100150", "names": ["RYR1-related myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "RYR1-related myopathy", "shortest_name_length": 21}
{"curie": "MONDO:0008979", "names": ["chorea familial benign", "chorea, benign familial", "CHOREA, BENIGN FAMILIAL", "Chorea, Benign Familial", "benign hereditary chorea"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chorea, benign familial", "shortest_name_length": 22}
{"curie": "MONDO:0013817", "names": ["PEE5", "Corin preeclampsia", "CORIN preeclampsia", "preeclampsia/eclampsia 5", "PREECLAMPSIA/eclampsia 5", "PREECLAMPSIA/ECLAMPSIA 5", "Preeclampsia/eclampsia type 5", "preeclampsia caused by mutation in Corin", "preeclampsia caused by mutation in CORIN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "preeclampsia/eclampsia 5", "shortest_name_length": 4}
{"curie": "UMLS:C0949047", "names": ["Factor III deficiency", "Factor III Deficiency", "Tissue Factor Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Factor III deficiency", "shortest_name_length": 21}
{"curie": "MONDO:0013589", "names": ["FSGS6", "focal segmental glomerulosclerosis 6", "FOCAL SEGMENTAL GLOMERULOSCLEROSIS 6", "glomerulosclerosis, focal segmental, 6", "GLOMERULOSCLEROSIS, FOCAL SEGMENTAL, 6", "MYO1E focal segmental glomerulosclerosis", "focal segmental glomerulosclerosis type 6", "focal segmental glomerulosclerosis caused by mutation in MYO1E"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal segmental glomerulosclerosis 6", "shortest_name_length": 5}
{"curie": "UMLS:C4727393", "names": ["Recurrent Minor Salivary Gland Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Minor Salivary Gland Adenocarcinoma", "shortest_name_length": 45}
{"curie": "UMLS:C1142498", "names": ["Application site excoriation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Application site excoriation", "shortest_name_length": 28}
{"curie": "MONDO:0003261", "names": ["cerebellar papillary meningioma", "Cerebellar Papillary Meningioma", "cerebellum papillary meningioma", "papillary meningioma of cerebellum", "Papillary Meningioma of Cerebellum", "Papillary meningioma of Cerebellum", "Papillary Meningioma of the Cerebellum", "papillary meningioma of the cerebellum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papillary meningioma of the cerebellum", "shortest_name_length": 31}
{"curie": "UMLS:C0035127", "names": ["rsi", "RSI", "Overuse Injury", "overuse injury", "Injury, Overuse", "Overuse injuries", "overuse injuries", "Overuse Syndrome", "Overuse Injuries", "Overuse syndrome", "overuse syndrome", "overuse syndromes", "Overuse Syndromes", "Overexertion syndrome", "Repetitive strain injury", "repetition strain injury", "Repetitive stress injury", "Repetitive motion injury", "Repetitive Strain Injury", "repetitive strain injury", "Repetition Strain Injury", "repetitive motion injury", "Repetitive Stress Injury", "Strain Injury, Repetition", "Injury, Repetitive Stress", "Injury, Repetitive Strain", "Strain Injury, Repetitive", "Injury, Repetition Strain", "Stress Injury, Repetitive", "Repetition Strain Injuries", "Repetitive motion disorder", "cumulative trauma disorder", "repetitive strain injuries", "Repetitive Motion Injuries", "Repetitive Motion Disorder", "Cumulative Trauma Disorder", "Repetitive Stress Injuries", "Repetitive Strain Injuries", "Cumulative Trauma Disorders", "Trauma Disorder, Cumulative", "Repetitive Motion Disorders", "Motion Disorder, Repetitive", "repetitive motion disorders", "cumulative trauma disorders", "Trauma Disorders, Cumulative", "overuse syndrome (diagnosis)", "Repetitive strain injury, NOS", "RSI - Repetitive strain injury", "Repetitive strain injury syndrome", "Repetitive motion disorder (disorder)", "RSIS - Repetitive strain injury syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cumulative Trauma Disorders", "shortest_name_length": 3}
{"curie": "UMLS:C0014089", "names": ["Encopresis", "encopresis", "Encopresis, NOS", "Nonorganic encopresis", "Functional encopresis", "functional encopresis", "encopresis (diagnosis)", "functional; encopresis", "Psychogenic encopresis", "Non-organic encopresis", "encopresis; functional", "Functional encopresis, NOS", "encopresis; nonorganic origin", "nonorganic origin; encopresis", "feces; incontinence, functional", "Encopresis of nonorganic origin", "Functional encopresis (finding)", "Incontinence of feces, psychological", "incontinence; fecal, nonorganic origin", "feces; incontinence, nonorganic origin", "Incontinence of feces of nonorganic origin", "Fecal incontinence not due to organic disease", "Faecal incontinence not due to organic disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Functional encopresis", "shortest_name_length": 10}
{"curie": "UMLS:C2983010", "names": ["Stage III Uterine Corpus Cancer", "Stage III Uterine Corpus Cancer AJCC v7", "Stage III Uterine (including Endometrial) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Uterine Corpus Cancer", "shortest_name_length": 31}
{"curie": "UMLS:C1112469", "names": ["Cytomegalovirus syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cytomegalovirus syndrome", "shortest_name_length": 24}
{"curie": "MONDO:0020606", "names": ["sex-linked disease", "sex chromosome disorder", "Sex chromosome disorder", "SEX CHROMOSOME DISORDER", "Sex Chromosome Disorder", "sex chromosome disorders", "Chromosome Disorder, Sex", "chromosomes disorder sex", "Sex Chromosome Disorders", "Chromosome Disorders, Sex", "Disorders, Sex Chromosome", "sex-linked hereditary disorder", "Sex-linked hereditary disorder", "Sex Linked Hereditary Disorders", "Hereditary disorder, sex linked", "Sex-linked hereditary disorder, NOS", "Sex Chromosome Abnormality Disorders", "Disorders, Sex Chromosome Abnormality", "Sex-linked hereditary disorder (disorder)", "sex-linked hereditary disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sex-linked disease", "shortest_name_length": 18}
{"curie": "MONDO:0030873", "names": ["CFNDS", "CARDIOFACIONEURODEVELOPMENTAL SYNDROME", "cardiofacioneurodevelopmental syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiofacioneurodevelopmental syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0020733", "names": ["Sym1", "SYM1", "SYM1A", "CUSHING SYMPHALANGISM", "Cushing symphalangism", "proximal symphalangism 1", "proximal symphalangism 1A", "symphalangism, proximal, 1A", "SYMPHALANGISM, PROXIMAL, 1A", "symphalangism, proximal, type 1A", "hereditary absence of the proximal interphalangeal joints", "HEREDITARY ABSENCE OF THE PROXIMAL INTERPHALANGEAL JOINTS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "proximal symphalangism 1A", "shortest_name_length": 4}
{"curie": "MONDO:0002911", "names": ["Brainstem glioma", "brainstem glioma", "Brainstem Glioma", "brain glioma stem", "Brain stem glioma", "Brain Stem Glioma", "brain stem glioma", "brain gliomas stem", "Glioma of Brainstem", "Glioma of brainstem", "glioma of brainstem", "glioma of brain stem", "Glioma of Brain Stem", "Glioma of the Brainstem", "glioma of the brainstem", "diffuse brainstem glioma", "Glioma of the Brain Stem", "glioma of the brain stem", "Diffuse brainstem glioma", "Brainstem Neuroglial tumor", "Brainstem Neuroglial Tumor", "brainstem malignant glioma", "brainstem neuroglial tumor", "brain stem neuroglial tumor", "Brain Stem Neuroglial Tumor", "brainstem neuroglial neoplasm", "Brainstem Neuroglial Neoplasm", "malignant glioma of brainstem", "Brain Stem Neuroglial Neoplasm", "Glioma of brainstem (disorder)", "brain stem neuroglial neoplasm", "glioma of brain stem (diagnosis)", "Diffuse midline glioma H3K27M mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brain stem glioma", "shortest_name_length": 16}
{"curie": "MONDO:0007906", "names": ["FPL2", "FPLD2", "Dunnigan Syndrome", "Dunnigan syndrome", "LIPOATROPHIC DIABETES", "reverse partial lipodystrophy", "Reverse Partial Lipodystrophy", "lipodystrophy, reverse partial", "LIPODYSTROPHY, REVERSE PARTIAL", "Lipodystrophy, Reverse Partial", "Partial Lipodystrophy, Reverse", "Reverse Partial Lipodystrophies", "Partial Lipodystrophies, Reverse", "Familial partial lipodystrophy type 2", "familial partial lipodystrophy type 2", "Familial Partial Lipodystrophy Type 2", "Familial Partial Lipodystrophy, Type 2", "Lipodystrophy, Familial Partial, Type 2", "lipodystrophy, familial partial, type 2", "LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2", "Familial partial lipodystrophy Dunnigan type", "familial partial lipodystrophy Dunnigan type", "Familial partial lipodystrophy, Dunnigan type", "familial partial lipodystrophy, Dunnigan type", "LIPODYSTROPHY, FAMILIAL PARTIAL, DUNNIGAN TYPE", "lipodystrophy, familial partial, Dunnigan type", "Lipodystrophy, Familial Partial, Dunnigan Type", "familial lipodystrophy of limbs and lower trunk", "Familial partial lipodystrophy type 2 (disorder)", "Lipodystrophy, Familial, of Limbs and Lower Trunk", "lipodystrophy, familial, of limbs and Lower trunk", "LIPODYSTROPHY, FAMILIAL, OF LIMBS AND LOWER TRUNK"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial partial lipodystrophy, Dunnigan type", "shortest_name_length": 4}
{"curie": "UMLS:C1968699", "names": ["Hypothyroidism, Thyroidal, With Spiky Hair And Cleft Palate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypothyroidism, Thyroidal, With Spiky Hair And Cleft Palate", "shortest_name_length": 59}
{"curie": "MONDO:0013248", "names": ["FANCO", "RAD51C Fanconi anemia", "Rad51C Fanconi anemia", "Fanconi anemia complementation group O", "FANCONI ANEMIA, COMPLEMENTATION GROUP O", "Fanconi Anemia, Complementation Group O", "Fanconi anemia, complementation group O", "Fanconi anemia complementation group type O", "Fanconi anemia caused by mutation in RAD51C", "Fanconi anemia caused by mutation in Rad51C", "Fanconi Anemia, complementation group type O", "Fanconi anemia complementation group O (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fanconi anemia complementation group O", "shortest_name_length": 5}
{"curie": "MONDO:0001707", "names": ["heart sarcoidosis", "Sarcoidosis cordis", "cardiac sarcoidosis", "Cardiac sarcoidosis", "Cardiac Sarcoidosis", "sarcoidosis of heart", "Heart sarcoid disease", "Cardiac sarcoidosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiac sarcoidosis", "shortest_name_length": 17}
{"curie": "MONDO:0800085", "names": ["dysostosis with predominant craniofacial involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dysostosis with predominant craniofacial involvement", "shortest_name_length": 52}
{"curie": "UMLS:C3898650", "names": ["Juvenile Amyopathic Dermatomyositis", "Juvenile Dermatomyositis Sine Myositis", "Juvenile Dermatomyositis sine Myositis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Juvenile Dermatomyositis Sine Myositis", "shortest_name_length": 35}
{"curie": "MONDO:0011676", "names": ["P-CIIS", "PHACE syndrome", "PHACE association", "PHACE ASSOCIATION", "Phaces association", "PHACES ASSOCIATION", "PHACES association", "aortic aneurysm, giant congenital", "AORTIC ANEURYSM, GIANT CONGENITAL", "pascual-Castroviejo syndrome type 2", "pascual-Castroviejo type II syndrome", "Posterior fossa brain malformations, hemangiomas of the face, arterial anomalies, cardiac anomalies, and eye abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PHACE syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0005284", "names": ["multiple sclerosis progressive", "Progressive multiple sclerosis", "progressive multiple sclerosis", "Multiple sclerosis (MS) progressive", "Chronic Progressive Multiple Sclerosis", "chronic progressive multiple sclerosis", "Chronic progressive multiple sclerosis", "multiple sclerosis chronic progressive", "Multiple Sclerosis, Chronic Progressive", "Progressive multiple sclerosis (disorder)", "Progressive multiple sclerosis (diagnosis)", "Chronic progressive multiple sclerosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic progressive multiple sclerosis", "shortest_name_length": 30}
{"curie": "UMLS:C1708670", "names": ["Leaflet Disruption Due To Suture Abrasion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leaflet Disruption Due To Suture Abrasion", "shortest_name_length": 41}
{"curie": "UMLS:C1710016", "names": ["Satellite Nodule", "Satellite nodules"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Satellite Nodule", "shortest_name_length": 16}
{"curie": "EFO:0005321", "names": ["molar-incisor hypomineralization"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "molar-incisor hypomineralization", "shortest_name_length": 32}
{"curie": "MONDO:0009732", "names": ["CnF", "CNF", "NPHS1", "nephrosis, congenital", "nephrotic syndrome type 1", "Nephrotic Syndrome, Type 1", "nephrotic syndrome, type 1", "NEPHROTIC SYNDROME, TYPE 1", "Congenital Finnish nephrosis", "FINNISH CONGENITAL NEPHROSIS", "finnish congenital nephrosis", "Finnish congenital nephrosis", "NEPHROTIC SYNDROME, CONGENITAL", "nephrotic syndrome, congenital", "Congenital nephrotic syndrome 1", "congenital nephrotic syndrome 1", "nephrotic syndrome congenital type 1", "Finnish congenital nephrotic syndrome", "Nephrosis 1, congenital, Finnish type", "nephrotic syndrome - NPHS1 associated", "nephrosis 1, congenital, Finnish type", "Nephrotic Syndrome - NPHS1 Associated", "finnish congenital nephrosis (diagnosis)", "congenital nephrotic syndrome Finnish type", "congenital nephrotic syndrome, Finnish type", "Congenital nephrotic syndrome, Finnish type", "CNF - Finnish congenital nephrotic syndrome", "Congenital Nephrotic Syndrome - Finnish Type", "Congenital nephrotic syndrome - finnish type", "congenital nephrotic syndrome - Finnish type", "Finnish congenital nephrotic syndrome (disorder)", "nephrotic syndrome congenital type 1 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital nephrotic syndrome, Finnish type", "shortest_name_length": 3}
{"curie": "UMLS:C0236748", "names": ["Organic anxiety syndrome", "organic anxiety disorder", "anxiety disorder organic", "Organic anxiety disorder", "organic anxiety syndrome", "anxiety disorder; organic", "organic; anxiety disorder", "disorder; anxiety, organic", "disorder; organic, anxiety", "organic; disorder, anxiety", "Organic anxiety disorder (disorder)", "Organic anxiety disorder (diagnosis)", "Anxiety disorder due to medical disorder", "medical condition; causing anxiety disorder", "anxiety disorder due to general medical condition", "Anxiety disorder due to general medical condition", "anxiety disorder; due to general medical condition", "Anxiety disorder due to a general medical condition", "Anxiety Disorder Due to Specified Medical Condition", "Anxiety Disorder Due to a General Medical Condition", "anxiety disorder due to general medical condition (diagnosis)", "Anxiety disorder due to a general medical condition (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anxiety disorder due to a general medical condition", "shortest_name_length": 24}
{"curie": "MONDO:0024239", "names": ["Congenital anomaly;cardiovas", "Congenital Cardiovascular Anomaly", "Congenital cardiovascular anomaly", "Congenital anomaly cardiovascular", "congenital cardiovascular anomaly", "congenital cardiovascular disorder", "Congenital Cardiovascular Disorder", "Congenital cardiovascular disorder", "congenital cardiovascular Abnormality", "Congenital Cardiovascular Abnormality", "Congenital cardiovascular anomaly NOS", "Cardiovascular malformation, congenital", "cardiovascular system development disease", "Congenital Anomaly of Cardiovascular System", "Congenital anomaly of cardiovascular system", "congenital anomaly of cardiovascular system", "Congenital cardiovascular disorder (disorder)", "disorder of cardiovascular system development", "Congenital anomalies heart/circulatory system", "congenital anomaly of the cardiovascular system", "congenital Abnormality of the circulatory system", "Congenital anomaly of cardiovascular system, NOS", "Congenital Abnormality of the Circulatory System", "CONGENITAL ANOMALIES OF THE CARDIOVASCULAR SYSTEM", "Congenital anomaly of cardiovascular system (disorder)", "congenital anomaly of cardiovascular system (diagnosis)", "CONGENITAL ANOMALIES OF THE CARDIOVASCULAR SYSTEM: GENERAL TERMS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital anomaly of cardiovascular system", "shortest_name_length": 28}
{"curie": "MONDO:0015288", "names": ["herpes eye", "eye herpes", "Herpes;eye", "eyes herpes", "HSV keratitis", "ocular herpes", "Herpes ocular", "HERPES OCULAR", "hsv keratitis", "herpes ocular", "Corneal herpes", "corneal herpes", "Furrow Keratitis", "KERATITIS HERPES", "herpes keratitis", "herpes ophthalmic", "ophthalmic herpes", "Herpes ophthalmic", "Keratitis, Furrow", "herpes of the eye", "Herpetic Keratitis", "Furrow Keratitides", "Keratitis herpetic", "herpetic keratitis", "Herpetic keratitis", "Keratitis, Herpetic", "Dendritic Keratitis", "dendritic keratitis", "keratitis dentritic", "Dendritic keratitis", "Keratitides, Furrow", "Keratitis, Dendritic", "Herpetic Keratitides", "ocular simplex herpes", "Ocular Herpes Simplex", "Dendritic Keratitides", "Herpes ophthalmic NOS", "Herpesvirus keratitis", "Keratitides, Herpetic", "ocular herpes simplex", "Simplexvirus keratitis", "Herpes Simplex, Ocular", "Keratitides, Dendritic", "HSV dendritic keratitis", "herpes simplex keratitis", "HERPES SIMPLEX KERATITIS", "Herpes Simplex Keratitis", "Herpes simplex keratitis", "Ophthalmic herpes simplex", "Herpes simplex;ophthalmic", "Keratitis, Herpes Simplex", "ophthalmic herpes simplex", "Herpes simplex ophthalmic", "Herpes Simplex Keratitides", "Keratitides, Herpes Simplex", "Herpes simplex ophthalmicus", "Keratitis due to Herpesvirus", "Simplexvirus caused keratitis", "herpes simplex virus keratitis", "Herpes simplex virus keratitis", "dendritic keratitis (diagnosis)", "dendritic Herpes simplex keratitis", "Herpes simplex dendritic keratitis", "Herpes simplex keratitis (disorder)", "Herpes simplex keratitis (diagnosis)", "Ophthalmic herpes simplex (disorder)", "dendritic keratitis (physical finding)", "Keratitis due to Herpesvirus (disorder)", "epithelial dendritic keratitis was observed", "Herpes simplex dendritic keratitis (disorder)", "dendritic Herpes simplex keratitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "herpes simplex virus keratitis", "shortest_name_length": 10}
{"curie": "UMLS:C4744520", "names": ["Frontal Lobe Anaplastic Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Frontal Lobe Anaplastic Astrocytoma", "shortest_name_length": 35}
{"curie": "UMLS:C2713321", "names": ["alpha L Iduronidase Deficiency", "alpha-L-Iduronidase Deficiency", "Alpha-L-iduronidase deficiency", "alpha-L-Iduronidase Deficiencies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alpha-L-Iduronidase Deficiency", "shortest_name_length": 30}
{"curie": "MONDO:0015849", "names": ["longitudinal vaginal septum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "longitudinal vaginal septum", "shortest_name_length": 27}
{"curie": "UMLS:C1333107", "names": ["Colorectal Adenoma with Moderate Dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Adenoma with Moderate Dysplasia", "shortest_name_length": 42}
{"curie": "MONDO:0006645", "names": ["alcoholic neuritis", "NEURITIS, ALCOHOLIC", "Neuropathy;alcoholic", "alcoholic neuropathy", "Alcoholic Neuropathy", "NEUROPATHY, ALCOHOLIC", "alcoholics neuropathy", "Neuropathy, Alcoholic", "Neuropathy, alcoholic", "alcoholic polyneuritis", "Alcoholic Polyneuritis", "Alcoholic Neuropathies", "alcoholic neuropathies", "alcohol; polyneuropathy", "alcoholics polyneuritis", "Polyneuritis, Alcoholic", "polyneuropathy; alcohol", "Neuropathies, Alcoholic", "Alcoholic polyneuropathy", "Alcoholic Polyneuropathy", "Alcoholic Polyneuritides", "alcoholic polyneuropathy", "Polyneuropathy alcoholic", "POLYNEUROPATHY ALCOHOLIC", "Polyneuropathy, Alcoholic", "polyneuropathy; alcoholic", "Polyneuritides, Alcoholic", "NEUROPATHY PERIPHERAL ETOH", "Alcoholic Polyneuropathies", "Polyneuropathies, Alcoholic", "Alcohol Related Polyneuropathy", "alcohol-related polyneuropathy", "Alcohol-Induced Polyneuropathy", "Alcohol-related polyneuropathy", "Alcohol-Related Polyneuropathy", "Alcohol-induced polyneuropathy", "Alcohol Induced Polyneuropathy", "alcoholic peripheral neuropathy", "Polyneuropathy, Alcohol-Induced", "Alcoholic peripheral neuropathy", "Polyneuropathy, Alcohol-Related", "Alcohol-Related Polyneuropathies", "Alcohol-Induced Polyneuropathies", "Polyneuropathies, Alcohol-Induced", "Polyneuropathies, Alcohol-Related", "Alcoholic polyneuropathy (disorder)", "alcoholic polyneuropathy (diagnosis)", "Alcohol-Induced Peripheral Neuropathy", "Alcohol Induced Peripheral Neuropathy", "Peripheral Neuropathy, Alcohol-Induced", "Peripheral Neuropathy, Alcohol Induced", "Neuropathy, Alcohol-Induced Peripheral", "Alcohol-Induced Peripheral Neuropathies", "Peripheral Neuropathies, Alcohol-Induced", "Alcohol-Related Autonomic Polyneuropathy", "Neuropathies, Alcohol-Induced Peripheral", "Alcohol Related Autonomic Polyneuropathy", "Autonomic Polyneuropathy, Alcohol-Related", "Polyneuropathy, Alcohol-Related Autonomic", "Alcohol-Related Autonomic Polyneuropathies", "Autonomic Polyneuropathies, Alcohol-Related", "Polyneuropathies, Alcohol-Related Autonomic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alcoholic polyneuropathy", "shortest_name_length": 18}
{"curie": "MONDO:0011420", "names": ["GHDP", "GHIP", "Short Stature, Idiopathic, Autosomal", "growth hormone insensitivity, partial", "GROWTH HORMONE INSENSITIVITY, PARTIAL", "Growth Hormone, Insensitivity To, Partial", "Growth hormone, insensitivity to, partial", "INCREASED RESPONSIVENESS TO GROWTH HORMONE", "increased responsiveness to Growth hormone", "GROWTH HORMONE DEFICIENCY, ISOLATED PARTIAL", "short stature due to partial GHR deficiency", "Growth hormone deficiency, isolated, partial", "Growth Hormone Deficiency, Isolated, Partial", "short stature due to partial growth hormone receptor deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short stature due to partial GHR deficiency", "shortest_name_length": 4}
{"curie": "UMLS:C5419539", "names": ["Unresectable Uveal Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Uveal Melanoma", "shortest_name_length": 27}
{"curie": "UMLS:C0086237", "names": ["Cryptogenic Epilepsy", "Epilepsy, Cryptogenic", "Cryptogenic Epilepsies", "Epilepsies, Cryptogenic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epilepsy, Cryptogenic", "shortest_name_length": 20}
{"curie": "MONDO:0044964", "names": ["oral cavity mucoepidermoid cancer", "Oral Cavity Mucoepidermoid Cancer", "oral cavity mucoepidermoid carcinoma", "Oral Cavity Mucoepidermoid Carcinoma", "mucoepidermoid carcinoma, oral cavity", "Mucoepidermoid Carcinoma of Oral Cavity", "mucoepidermoid carcinoma of oral cavity", "mucoepidermoid carcinoma of the oral cavity", "Mucoepidermoid carcinoma of the oral cavity", "Mucoepidermoid Carcinoma of the Oral Cavity", "mucoepidermoid carcinoma of oral cavity (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oral cavity mucoepidermoid carcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C5556699", "names": ["Advanced Non-Cutaneous Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Non-Cutaneous Melanoma", "shortest_name_length": 31}
{"curie": "MONDO:0011419", "names": ["camera Marugo Cohen syndrome", "Camera Marugo Cohen syndrome", "CAMERA-MARUGO-COHEN SYNDROME", "camera-Marugo-Cohen syndrome", "Camera-Marugo-Cohen Syndrome", "obesity, mental retardation, body asymmetry, and muscle weakness", "obesity, intellectual disability, body asymmetry, and muscle weakness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "camera-Marugo-Cohen syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0005224", "names": ["M1", "AWM", "AML M1", "FAB M1", "AML FAB-M1", "AML without maturation", "AML without Maturation", "Acute M1 Myeloid Leukemia", "acute M1 myeloid leukemia", "M1 acute myeloid leukemia", "M1 Acute Myeloid Leukemia", "Acute Myeloid Leukemia, M1", "Myeloid Leukemia, Acute, M1", "Leukemia, Myeloid, Acute, M1", "M1 acute myelocytic leukemia", "M1 Acute Myelogenous Leukemia", "M1 acute myelogenous leukemia", "M1 Acute Myeloblastic Leukemia", "M1 acute granulocytic leukemia", "acute myeloblastic leukemia M1", "Acute myeloblastic leukemia M1", "M1 acute myeloblastic leukemia", "acute myeloblastic leukemia type 1", "acute myeloid leukemia without maturation", "Acute myeloid leukemia without maturation", "Acute Myeloid Leukemia without Maturation", "Acute myeloid leukaemia without maturation", "M1 acute myeloid leukemia without maturation", "acute myelocytic leukemia without maturation", "M1 Acute Myeloid Leukemia without Maturation", "Acute myelocytic leukemia without maturation", "Acute Myelogenous Leukemia without Maturation", "Acute myelogenous leukemia without maturation", "acute myelogenous leukemia without maturation", "Acute myelocytic leukaemia without maturation", "Acute myelogenous leukaemia without maturation", "acute granulocytic leukemia without maturation", "Acute myeloblastic leukemia without maturation", "Acute Myeloblastic Leukemia without Maturation", "Acute granulocytic leukemia without maturation", "acute myeloblastic leukemia without maturation", "Acute granulocytic leukaemia without maturation", "M1 acute myelocytic leukemia without maturation", "Acute myeloblastic leukaemia without maturation", "M1 Acute Myelogenous Leukemia without Maturation", "M1 acute myelogenous leukemia without maturation", "M1 acute myeloblastic leukemia without maturation", "M1 Acute Myeloblastic Leukemia without Maturation", "Acute myeloid leukemia without maturation, FAB M1", "M1 acute granulocytic leukemia without maturation", "Acute myeloid leukaemia without maturation, FAB M1", "Acute Myeloid Leukemia without Maturation (FAB M1)", "acute myeloid leukemia without maturation (FAB M1)", "M1 - Acute myeloblastic leukemia without maturation", "acute myelogenous leukemia (AML) without maturation", "M1 - Acute myeloblastic leukaemia without maturation", "acute myelogenous leukemia without maturation (diagnosis)", "Acute myeloid leukemia without maturation, FAB M1 (disorder)", "Acute myeloid leukemia without maturation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloblastic leukemia without maturation", "shortest_name_length": 2}
{"curie": "UMLS:C3665905", "names": ["Passenger lymphocyte syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Passenger lymphocyte syndrome", "shortest_name_length": 29}
{"curie": "MONDO:0100021", "names": ["photosensitive occipital lobe epilepsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "photosensitive occipital lobe epilepsy", "shortest_name_length": 38}
{"curie": "MONDO:0014640", "names": ["FTDALS3", "frontotemporal dementia and/or amyotrophic lateral sclerosis-3", "frontotemporal dementia and/or amyotrophic lateral sclerosis 3", "FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 3", "frontotemporal dementia and/or amyotrophic lateral sclerosis type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontotemporal dementia and/or amyotrophic lateral sclerosis 3", "shortest_name_length": 7}
{"curie": "UMLS:C4055126", "names": ["Androgen Biosynthesis Defect", "Disorder of Androgen Synthesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disorder of Androgen Synthesis", "shortest_name_length": 28}
{"curie": "MONDO:0011444", "names": ["DURS2", "Duane syndrome type 2", "Duane syndrome, type 2", "Exotropic Duane syndrome", "Duane's syndrome, type 2", "type II Duane's syndrome", "Exotropic Duane's syndrome", "DUANE RETRACTION SYNDROME 2", "Duane Retraction Syndrome 2", "Duane retraction syndrome 2", "CHN1 Duane retraction syndrome", "Type 2 Duane Retraction Syndrome", "Duane retraction syndrome type 2", "Duane Retraction Syndrome, Type 2", "Duane's syndrome, type 2 (disorder)", "type II Duane's syndrome (diagnosis)", "Duane retraction syndrome caused by mutation in CHN1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Duane retraction syndrome 2", "shortest_name_length": 5}
{"curie": "MONDO:0017408", "names": ["ROHHAD", "ROHHADNET", "ROHHAD syndrome", "ROHHAD Syndrome", "rapid-onset obesity with hypothalamic dysfunction, hypoventilation and autonomic dysregulation", "Rapid-onset obesity with hypothalamic dysfunction, hypoventilation and autonomic dysregulation", "rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation", "Rapid-Onset Obesity with Hypothalamic Dysfunction, Hypoventilation, and Autonomic Dysregulation", "rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome", "Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome", "rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation syndrome", "Rapid-Onset Obesity with Hypothalamic Dysfunction, Hypoventilation, and Autonomic Dysregulation Syndrome", "Rapid-onset childhood obesity, hypothalamic dysfunction, hypoventilation, autonomic dysregulation syndrome", "ROHHAD (rapid-onset childhood obesity, hypothalamic dysfunction, hypoventilation, autonomic dysregulation) syndrome", "Rapid-onset childhood obesity, hypothalamic dysfunction, hypoventilation, autonomic dysregulation syndrome (disorder)", "rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation-neural tumors syndrome", "Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation-neural tumors syndrome", "ROHHADNET (rapid-onset childhood obesity, hypothalamic dysfunction, hypoventilation, autonomic dysregulation, neural tumors) syndrome", "ROHHADNET (rapid-onset childhood obesity, hypothalamic dysfunction, hypoventilation, autonomic dysregulation, neural tumours) syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0017778", "names": ["LI", "Lamellar Ichthyosis", "lamellar ichthyosis", "classic lamellar ichthyosis", "congenital lamellar ichthyosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lamellar ichthyosis", "shortest_name_length": 2}
{"curie": "MONDO:0016446", "names": ["acquired cutis laxa", "Acquired cutis laxa", "Cutis laxa acquisita", "cutis laxa acquisita", "Cutis laxa, acquired type", "Cutis laxa, acquired type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired cutis laxa", "shortest_name_length": 19}
{"curie": "MONDO:0004276", "names": ["Ceruminoma", "ceruminoma", "Ceruminous adenoma", "Ceruminous Adenoma", "ceruminous adenoma", "ceruminous; adenoma", "adenoma; ceruminous", "Ceruminous gland adenoma", "Ceruminous adenoma (disorder)", "Adenoma of the ceruminous gland", "Neoplasm of the ceruminal gland", "adenoma, ceruminous gland, benign", "ADENOMA, CERUMINOUS GLAND, BENIGN", "External Auditory Canal Ceruminous Adenoma", "external auditory canal ceruminous adenoma", "ceruminous adenoma (morphologic abnormality)", "Ceruminous adenoma (morphologic abnormality)", "Ceruminous Adenoma of External Auditory Canal", "ceruminous adenoma of external auditory canal", "ceruminous adenoma of the external auditory canal", "Ceruminous Adenoma of the External Auditory Canal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ceruminoma", "shortest_name_length": 10}
{"curie": "MONDO:0005689", "names": ["Pot", "Weed", "Hash", "Cannabis", "Marijuana", "marijuana", "Cannabis abuse", "Cannabis Abuse", "cannabis abuse", "abuse cannabis", "Abuse, Cannabis", "Marijuana abuse", "Marihuana Abuse", "Marijuana Abuse", "abuse; cannabis", "marijuana abuse", "cannabis; abuse", "abuse marijuana", "marihuana; abuse", "abuse; marihuana", "Abuse, Marihuana", "Abuse, Marijuana", "ganja; dependence", "dependence; ganja", "Cannabis addiction", "Cannabis dependence", "maconha; dependence", "Cannabis Dependence", "marijuana addiction", "dependence; maconha", "cannabis dependence", "Dependence, Cannabis", "drug abuse marijuana", "DRUG ABUSE MARIJUANA", "Marijuana dependence", "dependence; cannabis", "marijuana drug abuse", "cannabis; dependence", "Marijuana Dependence", "abuse drug marijuana", "marijuana dependence", "marihuana; dependence", "Dependence, Marijuana", "dependence; marihuana", "Dependence on cannabis", "Abuse;drug(s);marijuana", "Dependence on marijuana", "Cannabis abuse (disorder)", "cannabis abuse (diagnosis)", "Addiction;drug(s);marijuana", "Cannabis dependence (disorder)", "DRUG ABUSE MARIJUANA DEPENDENCE", "cannabis dependence (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cannabis dependence", "shortest_name_length": 3}
{"curie": "MONDO:0012662", "names": ["USH2D", "WHRN Usher syndrome", "Usher syndrome type 2D", "Usher Syndrome, Type II", "Usher syndrome, type 2D", "Usher syndrome type IID", "Usher Syndrome, Type IId", "USHER SYNDROME, TYPE IID", "USHER syndrome, type IID", "Usher syndrome caused by mutation in WHRN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Usher syndrome type 2D", "shortest_name_length": 5}
{"curie": "UMLS:C5401355", "names": ["Odontogenic Carcinoma", "Odontogenic carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Odontogenic Carcinoma", "shortest_name_length": 21}
{"curie": "UMLS:C3274500", "names": ["NADH Dehydrogenase Deficiency", "NADH-CoQ Reductase (Complex I) Deficiency", "NADH Dehydrogenase (Ubiquinone) Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "NADH Dehydrogenase Deficiency", "shortest_name_length": 29}
{"curie": "MONDO:0017556", "names": ["Madelung deformity, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Madelung deformity, unilateral", "shortest_name_length": 30}
{"curie": "MONDO:0005720", "names": ["yaba", "COWPOX", "cowpox", "Cowpox", "cow pox", "Cow Pox", "Cow pox", "Pox, Cow", "Cowpox (disorder)", "cowpox (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cowpox", "shortest_name_length": 4}
{"curie": "MONDO:0013967", "names": ["PEX14B", "peroxisome biogenesis disorder 14B", "PEROXISOME BIOGENESIS DISORDER 14B", "PEX11B peroxisome biogenesis disorder", "peroxisome biogenesis disorder type 14B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder 14B", "shortest_name_length": 6}
{"curie": "UMLS:C0919607", "names": ["Duodenal NET G1", "Duodenal Carcinoid Tumor", "Carcinoid Tumor of Duodenum", "Carcinoid Tumor of the Duodenum", "Carcinoid tumor of the duodenum", "Duodenal Neuroendocrine Tumor G1", "Carcinoid tumour of the duodenum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carcinoid tumor of the duodenum", "shortest_name_length": 15}
{"curie": "UMLS:C4725821", "names": ["Refractory Malignant Skin Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Malignant Skin Neoplasm", "shortest_name_length": 34}
{"curie": "MONDO:0044745", "names": ["neurological injury", "Injury;neurological", "injury neurological", "Neurological Damage", "Neurological injury", "craniocervical injury", "Nervous System Trauma", "Nervous System Injury", "Nervous system injury", "injuries neurological", "nervous system injury", "nervous system trauma", "nervous system Traumas", "injury, nervous system", "injury, craniocervical", "Nervous System Traumas", "Trauma, Nervous System", "injuries nervous system", "Nervous System Injuries", "nervous system Injuries", "craniocervical Injuries", "nervous system injuries", "Injuries, Nervous System", "Injuries, craniocervical", "Injuries, nervous system", "injury of nervous system", "Injury of nervous system", "nervous system disorder injury", "Injury of nervous system (disorder)", "Injury of nervous system (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nervous system injury", "shortest_name_length": 19}
{"curie": "UMLS:C4683606", "names": ["Lugano Classification Limited Stage Adult Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Limited Stage Adult Hodgkin Lymphoma AJCC v8", "shortest_name_length": 66}
{"curie": "UMLS:C1334761", "names": ["Middle Ear Paraganglioma", "Paraganglioma of Middle Ear", "Paraganglioma of the Middle Ear", "Non-Chromaffin Middle Ear Paraganglioma", "Non-Chromaffin Paraganglioma of Middle Ear", "Non-Chromaffin Paraganglioma of the Middle Ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Middle Ear Paraganglioma", "shortest_name_length": 24}
{"curie": "UMLS:C0267482", "names": ["Coloenteric fistula", "enterocolic fistula", "coloenteric fistula", "Enterocolic fistula", "fistula; enterocolic", "entero-colic fistula", "enterocolic; fistula", "Enterocolonic fistula", "enterocolonic fistula", "Enterocolic fistula (disorder)", "entero-colic fistula (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Enterocolic fistula", "shortest_name_length": 19}
{"curie": "MONDO:0019688", "names": ["sulphation disorder", "inborn error of sulphation", "sulfation-related bone disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sulfation-related bone disorder", "shortest_name_length": 19}
{"curie": "MONDO:0045039", "names": ["systemic basidiobolomycosis", "disseminated basidiobolomycosis", "Disseminated basidiobolomycosis", "Disseminated basidiobolomycosis (disorder)", "Disseminated basidiobolomycosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "systemic basidiobolomycosis", "shortest_name_length": 27}
{"curie": "UMLS:C0235213", "names": ["EJACULATION DECREASED", "Ejaculation decreased"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ejaculation decreased", "shortest_name_length": 21}
{"curie": "MONDO:0001924", "names": ["Dystrophies primarily involving the retinal pigment epithelium", "dystrophies primarily involving the retinal pigment epithelium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dystrophies primarily involving the retinal pigment epithelium", "shortest_name_length": 62}
{"curie": "MONDO:0002928", "names": ["MMMT", "Carcinosarcoma", "carcinosarcoma", "Carcinosarcomas", "Mullerian tumor", "carcinosarcomas", "Carcinosarcoma NOS", "Carcinosarcoma, NOS", "mixed Mullerian tumor", "Mixed Müllerian Tumor", "Mixed Mullerian Tumor", "mullerian mixed tumor", "Mullerian mixed tumor", "MULLERIAN MIXED TUMOR", "mixed mullerian tumor", "Mullerian Mixed Tumor", "Tumor, Mullerian Mixed", "mesodermal mixed tumor", "Mesodermal mixed tumor", "mixed mullerian tumour", "mullerian mixed tumour", "mixed tumor, Mullerian", "mixed mesodermal tumor", "Mesodermal Mixed Tumor", "Mullerian mixed tumour", "Mixed Tumor, Mullerian", "mixed mullerian tumors", "Mixed Tumor, Mesodermal", "Mesodermal mixed tumour", "mixed mesodermal tumors", "Mesodermal Mixed Tumors", "Tumor, Mesodermal Mixed", "Mixed Tumors, Mesodermal", "Tumors, Mesodermal Mixed", "CARCINOSARCOMA, MALIGNANT", "carcinosarcoma, malignant", "Carcinosarcoma, embryonal", "carcinosarcoma (diagnosis)", "Malignant Mixed Müllerian Tumor", "Malignant Mixed Mullerian Tumor", "malignant mixed Mullerian tumor", "Malignant mixed mesodermal tumor", "Malignant Mixed Mesodermal Tumor", "Mullerian mixed tumor (diagnosis)", "Malignant mixed mesodermal tumour", "MULLERIAN TUMOR, MIXED, MALIGNANT", "mesodermal mixed tumor (diagnosis)", "mixed Mesodermal (mullerian) tumor", "Mixed Mesodermal (Mullerian) Tumor", "mixed mesodermal (mullerian) tumor", "Mixed Mesodermal (Müllerian) Tumor", "Mixed Mesodermal (Mullerian) Neoplasm", "Mixed Mesodermal (Müllerian) Neoplasm", "Carcinosarcoma (morphologic abnormality)", "Malignant Mixed Mesodermal (Mullerian) Tumor", "malignant mixed mesodermal (mullerian) tumor", "Malignant Mixed Mesodermal (Müllerian) Tumor", "mullerian mixed tumor (morphologic abnormality)", "mesodermal mixed tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinosarcoma", "shortest_name_length": 4}
{"curie": "MONDO:0013195", "names": ["CMH13", "hypertrophic cardiomyopathy 13", "cardiomyopathy, hypertrophic, 13", "TNNC1 hypertrophic cardiomyopathy", "hypertrophic cardiomyopathy type 13", "cardiomyopathy familial hypertrophic 13", "CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 13", "Cardiomyopathy, Familial Hypertrophic, 13", "cardiomyopathy, familial hypertrophic, 13", "cardiomyopathy, familial hypertrophic, type 13", "hypertrophic cardiomyopathy caused by mutation in TNNC1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophic cardiomyopathy 13", "shortest_name_length": 5}
{"curie": "MONDO:0012822", "names": ["CRCS6", "COLORECTAL CANCER, SUSCEPTIBILITY TO, 6", "colorectal cancer, susceptibility to, 6", "COLORECTAL CANCER, SUSCEPTIBILITY TO, ON CHROMOSOME 8q23", "colorectal cancer, susceptibility to, on chromosome 8Q23"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorectal cancer, susceptibility to, 6", "shortest_name_length": 5}
{"curie": "MONDO:0018368", "names": ["PPSPC", "peritoneal serous papillary adenocarcinoma", "Primary peritoneal serous/papillary carcinoma", "Primary Peritoneal Serous Papillary Carcinoma", "primary peritoneal serous papillary carcinoma", "primary peritoneal serous/papillary carcinoma", "primary serous papillary carcinoma of peritoneum", "Primary serous papillary carcinoma of peritoneum", "Primary Serous Papillary Carcinoma of Peritoneum", "primary peritoneal serous papillary adenocarcinoma", "Primary Peritoneal Serous Papillary Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary peritoneal serous/papillary carcinoma", "shortest_name_length": 5}
{"curie": "MONDO:0027462", "names": ["ARCL2C", "autosomal recessive cutis laxa type 2C", "autosomal recessive cutis laxa type IIC", "cutis laxa, autosomal recessive, type 2C", "CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC", "cutis laxa, autosomal recessive, type IIC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive cutis laxa type 2C", "shortest_name_length": 6}
{"curie": "MONDO:0014848", "names": ["YHFS", "YOU-HOOVER-FONG SYNDROME", "you-Hoover-Fong syndrome", "You Hoover Fong syndrome", "You-Hoover-Fong syndrome", "TELO2-related intellectual disability-neurodevelopmental disorder", "TELO2-related intellectual disability, neurodevelopmental disorder", "Telomere maintenance 2-related intellectual disability, neurodevelopmental disorder", "Telomere maintenance 2-related intellectual disability, neurodevelopmental disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "TELO2-related intellectual disability-neurodevelopmental disorder", "shortest_name_length": 4}
{"curie": "UMLS:C5205548", "names": ["Unresectable Ovarian Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Ovarian Serous Adenocarcinoma", "shortest_name_length": 42}
{"curie": "UMLS:C4054383", "names": ["Nephrotic Syndrome - INF2 Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - INF2 Associated", "shortest_name_length": 36}
{"curie": "MONDO:0002970", "names": ["ciliary body disease", "Ciliary Body Disease", "ciliary body disorder", "Ciliary body disorder", "Ciliary Body Disorder", "disease of ciliary body", "Disorder of ciliary body", "disorder of ciliary body", "Disorder of ciliary body, NOS", "ciliary body disease or disorder", "Disorder of ciliary body (disorder)", "disease or disorder of ciliary body", "disease (or disorder); body, ciliary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ciliary body disorder", "shortest_name_length": 20}
{"curie": "MONDO:0035734", "names": ["hereditary angioedema with normal C1inh not related to F12 or PLG variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary angioedema with normal C1inh not related to F12 or PLG variant", "shortest_name_length": 73}
{"curie": "MONDO:0006480", "names": ["Xanthosarcoma", "inflammatory MFH", "Inflammatory MFH", "Malignant Xanthogranuloma", "malignant xanthogranuloma", "malignant inflammatory fibrous histiocytoma", "Inflammatory Malignant Fibrous Histiocytoma", "inflammatory malignant fibrous histiocytoma", "Inflammatory malignant fibrous histiocytoma", "Undifferentiated Pleomorphic Sarcoma, Inflammatory Variant", "undifferentiated pleomorphic sarcoma, inflammatory variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "undifferentiated pleomorphic sarcoma, inflammatory variant", "shortest_name_length": 13}
{"curie": "MONDO:0010811", "names": ["BPH", "bph", "Prostatauxe", "prostate hyperplasia", "PROSTATE HYPERTROPHY", "prostate hypertrophy", "prostate; hypertrophy", "Prostatic hyperplasia", "Prostatic Hypertrophy", "prostate; hyperplasia", "Prostate--Hypertrophy", "hyperplasia; prostate", "prostatic hyperplasia", "hypertrophy; prostate", "PROSTATIC HYPERTROPHY", "Hyperplasia;prostatic", "Prostatic hypertrophy", "prostatic hypertrophy", "Prostatic Hyperplasia", "Hypertrophy, Prostatic", "Hyperplasia, Prostatic", "Prostatic Hypertrophies", "Hyperplasia of prostate", "Enlarged Prostate (BPH)", "benign enlarged prostate", "Benign myoma of prostate", "Hypertrophies, Prostatic", "Enlarged prostate (benign)", "Prostatic area hypertrophy", "Benign fibroma of prostate", "benign prostate enlargement", "PROSTATE HYPERPLASIA BENIGN", "benign prostate hyperplasia", "PROSTATE HYPERTROPHY BENIGN", "benign prostate hypertrophy", "Hypertrophy of prostate NOS", "Hyperplasia of prostate NOS", "Hyperplasia of the prostate", "Benign Prostate Hyperplasia", "Benign prostatic hyperplasia", "Benign Prostatic Hyperplasia", "Benign prostatic hypertrophy", "Hyperplasia of prostate, NOS", "benign prostatic Hypertrophy", "benign prostatic hyperplasia", "benign prostatic hypertrophy", "Benign Prostatic Hypertrophy", "Benign Prostatic Hyperplasias", "Hyperplasia, Benign Prostatic", "Prostatic Hyperplasia, Benign", "PROSTATIC HYPERPLASIA, BENIGN", "prostatic hyperplasia, benign", "Hypertrophy, Benign Prostatic", "PROSTATE, HYPERTROPHY, BENIGN", "Prostatic Hypertrophy, Benign", "Hyperplasias, Benign Prostatic", "Prostatic Hyperplasias, Benign", "benign hyperplasia of prostate", "Prostatic hypertrophy (benign)", "Benign enlargement of prostate", "PROSTATE, HYPERPLASIA, NODULAR", "Benign Hyperplasia of Prostate", "Hypertrophy (benign) of prostate", "Benign prostatic hyperplasia, NOS", "prostatic hyperplasia (diagnosis)", "Benign hypertrophy of prostate NOS", "Benign prostatic hyperplasia (BPH)", "BPH (benign prostatic hypertrophy)", "benign prostatic hyperplasia - BPH", "Benign Hyperplasia of the Prostate", "benign prostatic hyperplasia (BPH)", "Benign Prostatic Hyperplasia - BPH", "benign hypertrophy of the prostate", "Hyperplasia of prostate (disorder)", "benign hyperplasia of the prostate", "BPH - Benign prostatic hypertrophy", "BPH - benign prostatic hyperplasia", "Benign enlargement of prostate, NOS", "Hyperplasia of prostate, unspecified", "BEP - Benign enlargement of prostate", "Nodular hyperplasia of prostate gland", "Lobular hyperplasia of prostate gland", "benign prostatic hyperplasia (disease)", "Benign prostatic hyperplasia (disorder)", "benign prostatic hypertrophy (diagnosis)", "adenofibromatous hypertrophy of prostate", "Adenofibromatous hypertrophy of prostate", "PROSTATIC HYPERPLASIA BENIGN <PROSTATISM>", "Fibromuscular hyperplasia of prostate gland", "Adenomyomatous hyperplasia of prostate gland", "Adenofibromatous hypertrophy of prostate, NOS", "adenofibromatous hypertrophy of prostate (diagnosis)", "Glandular, stromal and muscular hyperplasia of prostate", "Glandular, stromal and muscular hyperplasia of prostate gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign prostatic hyperplasia", "shortest_name_length": 3}
{"curie": "MONDO:0017029", "names": ["Langerhans cell histiocytosis", "Langerhans Cell Histiocytosis", "adult Langerhans cell histiocytosis", "Adult Langerhans Cell Histiocytosis", "histiocytosis X specific to adulthood", "Langerhans cell histiocytosis specific to adulthood", "Langerhans cell granulomatosis specific to adulthood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Langerhans cell histiocytosis specific to adulthood", "shortest_name_length": 29}
{"curie": "UMLS:C0233818", "names": ["Impaired Judgment", "impairs judgement", "impaired judgment", "Judgment Impaired", "Impaired judgement", "Defective judgment", "impaired judgement", "Impaired Judgement", "Judgement impaired", "JUDGEMENT IMPAIRED", "JUDGMENT IMPAIRMENT", "Defective judgement", "Impaired judgement (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Impaired judgement", "shortest_name_length": 17}
{"curie": "UMLS:C0877405", "names": ["Smooth muscle cell neoplasm", "Smooth muscle cell neoplasm NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Smooth muscle cell neoplasm", "shortest_name_length": 27}
{"curie": "UMLS:C4683599", "names": ["Lugano Classification Stage IIE Childhood Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage IIE Childhood Hodgkin Lymphoma AJCC v8", "shortest_name_length": 66}
{"curie": "MONDO:0800145", "names": ["non-severe combined immunodeficiency due to polymerase delta deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-severe combined immunodeficiency due to polymerase delta deficiency", "shortest_name_length": 71}
{"curie": "MONDO:0004299", "names": ["Infiltrating Bladder Lymphoepithelioma-Like Carcinoma", "infiltrating bladder lymphoepithelioma-like carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infiltrating bladder lymphoepithelioma-like carcinoma", "shortest_name_length": 53}
{"curie": "UMLS:C1285375", "names": ["Musculoskeletal Neoplasm", "musculoskeletal neoplasm", "Neoplasm;musculoskeletal", "Musculoskeletal System Neoplasm", "Neoplasm of musculoskeletal system", "neoplasm of the musculoskeletal system", "Neoplasm of musculoskeletal system (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplasm of musculoskeletal system", "shortest_name_length": 24}
{"curie": "MONDO:0022398", "names": ["aglossia and situs inversus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aglossia and situs inversus", "shortest_name_length": 27}
{"curie": "UMLS:C1333506", "names": ["Extrahepatic Bile Duct Fibroma", "Fibroma of Extrahepatic Bile Duct", "Fibroma of the Extrahepatic Bile Duct"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extrahepatic Bile Duct Fibroma", "shortest_name_length": 30}
{"curie": "MONDO:0011310", "names": ["long chain fatty acids, defect in TRANSPORT OF", "LONG CHAIN FATTY ACIDS, DEFECT IN TRANSPORT OF", "long chain fatty acids, defect in transport of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "long chain fatty acids, defect in transport of", "shortest_name_length": 46}
{"curie": "MONDO:0018167", "names": ["primary essential cutis verticis gyrata", "Primary essential cutis verticis gyrata", "Primary essential cutis verticis gyrata (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary essential cutis verticis gyrata", "shortest_name_length": 39}
{"curie": "UMLS:C4521726", "names": ["Stage III Esophageal Squamous Cell Cancer", "Clinical Stage III Esophageal Squamous Cell Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage III Esophageal Squamous Cell Carcinoma AJCC v8", "shortest_name_length": 41}
{"curie": "MONDO:0016651", "names": ["UPD(1)mat", "maternal uniparental disomy of chromosome 1", "maternal uniparental disomy of chromosome type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maternal uniparental disomy of chromosome 1", "shortest_name_length": 9}
{"curie": "UMLS:C1142550", "names": ["Native Valve Endocarditis", "native valve endocarditis", "endocarditis native valve", "Native valve endocarditis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Native valve endocarditis", "shortest_name_length": 25}
{"curie": "UMLS:C1706684", "names": ["Abnormality of Ventricle"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abnormality of Ventricle", "shortest_name_length": 24}
{"curie": "UMLS:C0268854", "names": ["bladder contracts", "contracted bladder", "Contracted bladder", "bladder contracted", "bladder contraction", "contraction; bladder", "Contracted bladder (disorder)", "contracted bladder (diagnosis)", "bladder contraction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Contracted bladder", "shortest_name_length": 17}
{"curie": "MONDO:0033560", "names": ["MC1DN35", "nuclear type mitochondrial complex I deficiency 35", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 35", "mitochondrial complex 1 deficiency, nuclear type 35"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 35", "shortest_name_length": 7}
{"curie": "MONDO:0026771", "names": ["DEE85", "EIEE85", "early infantile epileptic encephalopathy 85", "DEE85, with or without midline brain defects", "developmental and epileptic encephalopathy 85", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 85 WITH OR WITHOUT MIDLINE BRAIN DEFECTS", "epileptic encephalopathy, early infantile, 85, with or without midline brain defects", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 85, WITH OR WITHOUT MIDLINE BRAIN DEFECTS", "developmental and epileptic encephalopathy, 85, with or without midline brain defects", "developmental and epileptic encephalopathy 85, with or without midline brain defects, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 85, with or without midline brain defects", "shortest_name_length": 5}
{"curie": "UMLS:C1334735", "names": ["Metastatic Non-Cutaneous Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Non-Cutaneous Melanoma", "shortest_name_length": 33}
{"curie": "MONDO:0033545", "names": ["MTDPS19", "mitochondrial DNA depletion syndrome 19", "MITOCHONDRIAL DNA DEPLETION SYNDROME 19"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial DNA depletion syndrome 19", "shortest_name_length": 7}
{"curie": "UMLS:C0022492", "names": ["Erotomania", "erotomania", "Kandinsky Syndrome", "Clerambault Syndrome", "Erotomania (disorder)", "erotomania (diagnosis)", "Clerambault's syndrome", "clerambault's syndrome", "De Clerambault's syndrome", "de clerambault's syndrome", "deviation; sexual, erotomania", "sexual; deviation, erotomania"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kandinsky Syndrome", "shortest_name_length": 10}
{"curie": "UMLS:C1336467", "names": ["Stage 1 Neuroblastoma", "Stage I Neuroblastoma", "stage 1 neuroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 1 Neuroblastoma", "shortest_name_length": 21}
{"curie": "MONDO:0004624", "names": ["uvula cancer", "malignant uvula tumor", "palatine uvula cancer", "Malignant Uvula Tumor", "Malignant Uvular Tumor", "malignant Uvular tumor", "malignant uvular tumor", "Malignant Uvula Tumour", "malignant uvula tumour", "Malignant Uvular Tumour", "malignant uvular tumour", "Malignant tumor of uvula", "cancer of palatine uvula", "malignant uvula neoplasm", "Malignant Uvula Neoplasm", "malignant tumor of uvula", "malignant uvular neoplasm", "Malignant tumour of uvula", "Malignant Uvular Neoplasm", "Malignant neoplasm of uvula", "malignant neoplasm of uvula", "malignant palatine uvula neoplasm", "Malignant tumor of uvula (disorder)", "malignant neoplasm of palatine uvula", "malignant neoplasm of uvula (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uvula cancer", "shortest_name_length": 12}
{"curie": "MONDO:0016770", "names": ["Actinic LP", "actinic LP", "Actinic lichen planus", "lichen planus actinus", "actinic lichen planus", "lichen planus actinic", "Lichen planus actinus", "Lichen planus tropicus", "lichen planus tropicus", "Lichen planus actinicus", "lichen planus subtropicus", "Lichen planus subtropicus", "lichenoid melanodermatitis", "Lichenoid melanodermatitis", "Actinic lichen planus (disorder)", "summertime actinic lichenoid eruption", "Summertime actinic lichenoid eruption"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "actinic lichen planus", "shortest_name_length": 10}
{"curie": "UMLS:C0854804", "names": ["CLL Stage IV", "Stage IV CLL", "CLL, stage IV", "Metastatic CLL", "Chronic lymphocytic leukemia stage 4", "Chronic Lymphocytic Leukemia Stage IV", "Stage IV Chronic Lymphocytic Leukemia", "stage IV chronic lymphocytic leukemia", "Chronic lymphocytic leukaemia stage 4", "chronic lymphocytic leukemia, stage IV", "lymphocytic leukemia, stage IV chronic", "leukemia, stage IV chronic lymphocytic", "Metastatic Chronic Lymphocytic Leukemia", "Chronic lymphocytic leukemia stage C(IV)", "Chronic lymphocytic leukaemia stage C(IV)", "Stage IV Chronic Lymphocytic Leukemia (CLL)", "Stage IV Chronic Lymphocytic Leukemia- Modified Rai Staging System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic lymphocytic leukemia stage 4", "shortest_name_length": 12}
{"curie": "UMLS:C4552224", "names": ["B-Cell Aplasia", "B-cell aplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-cell aplasia", "shortest_name_length": 14}
{"curie": "UMLS:C4727580", "names": ["Sinonasal Poorly Differentiated Carcinoma", "Nasal Cavity and Paranasal Sinus Poorly Differentiated Carcinoma", "Poorly Differentiated Carcinoma of the Nasal Cavity and/or Paranasal Sinuses"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Poorly Differentiated Carcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0013071", "names": ["EDMD4", "Emery-Dreifuss muscular dystrophy 4", "Emery-Dreifuss Muscular Dystrophy 4", "Emery-Dreifuss muscular dystrophy 4 (diagnosis)", "autosomal dominant Emery-Dreifuss muscular dystrophy 4", "EMERY-Dreifuss muscular dystrophy 4, autosomal dominant", "EMERY-DREIFUSS MUSCULAR DYSTROPHY 4, AUTOSOMAL DOMINANT", "Emery-Dreifuss muscular dystrophy 4, autosomal dominant", "Emery-Dreifuss Muscular Dystrophy 4, Autosomal Dominant", "Emery-Dreifuss muscular dystrophy 4 with variable features", "EMERY-DREIFUSS MUSCULAR DYSTROPHY 4 WITH VARIABLE FEATURES", "SYNE1 autosomal dominant Emery-Dreifuss muscular dystrophy", "autosomal dominant Emery-Dreifuss muscular dystrophy caused by mutation in SYNE1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Emery-Dreifuss muscular dystrophy 4, autosomal dominant", "shortest_name_length": 5}
{"curie": "UMLS:C1292780", "names": ["t-MDS", "Therapy-Related MDS", "Therapy Related Myelodysplastic Syndrome", "Therapy-Related Myelodysplastic Syndrome", "therapy-related myelodysplastic syndrome", "Therapy-related myelodysplastic syndrome", "Therapy-related myelodysplastic syndrome (disorder)", "therapy-related myelodysplastic syndrome (diagnosis)", "Therapy-related myelodysplastic syndrome, alkylating agent related", "Therapy-related myelodysplastic syndrome (morphologic abnormality)", "Therapy-related myelodysplastic syndrome, epidopophyllotoxin-related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Therapy-related myelodysplastic syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0521596", "names": ["Jejunal hemorrhage", "Jejunal Hemorrhage", "Hemorrhage jejunum", "HEMORRHAGE JEJUNUM", "Jejunal haemorrhage", "Haemorrhage jejunum", "HEMORRHAGE OF JEJUNUM", "Hemorrhage of jejunum", "Haemorrhage of jejunum", "Hemorrhage of jejunum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jejunal hemorrhage", "shortest_name_length": 18}
{"curie": "MONDO:0015250", "names": ["Hamano Tsukamoto syndrome", "Hamano-Tsukamoto syndrome", "Spinal atrophy-ophthalmoplegia-pyramidal syndrome", "spinal atrophy ophthalmoplegia pyramidal syndrome", "spinal atrophy-ophthalmoplegia-pyramidal syndrome", "Spinal atrophy, ophthalmoplegia, pyramidal syndrome", "Spinal atrophy, ophthalmoplegia, pyramidal syndrome (disorder)", "infantile progressive spinal muscular atrophy with ophthalmoplegia and pyramidal symptoms"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal atrophy-ophthalmoplegia-pyramidal syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0001751", "names": ["cholestases", "Cholestases", "CHOLESTASIS", "cholestasis", "bile stasis", "Bile stasis", "Cholestasis", "bile; stasis", "stasis; bile", "bile occlusion", "BILIARY STASIS", "biliary stasis", "Biliary Stasis", "Biliary stasis", "Biliary Stases", "Stasis, Biliary", "Stases, Biliary", "bile obstruction", "Bile stasis, NOS", "Cholestasis, NOS", "bile duct occlusion", "Bile duct occlusion", "occlusion; bile duct", "bile duct; occlusion", "bile duct obstruction", "BILE DUCT OBSTRUCTION", "obstruction bile duct", "Bile duct obstruction", "Bile Duct Obstruction", "Cholestasis (finding)", "Occlusion of bile duct", "bile ducts obstruction", "Obstruction, Bile Duct", "obstruction; bile duct", "Bile Duct Obstructions", "bile duct; obstruction", "Duct Obstruction, Bile", "Obstructions, Bile Duct", "Duct Obstructions, Bile", "bile ducts obstructions", "biles ducts obstruction", "of bile duct obstruction", "biles ducts obstructions", "Obstruction of bile duct", "obstruction of bile duct", "Bile duct obstruction NOS", "d.choledochus; obstruction", "Occlusion of bile duct, NOS", "Obstruction of bile duct, NOS", "bile duct occlusion (diagnosis)", "Occlusion of bile duct (disorder)", "Obstruction of bile duct (disorder)", "obstruction of bile duct (diagnosis)", "Slowed or blocked flow of bile from liver"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholestasis", "shortest_name_length": 11}
{"curie": "MONDO:0001158", "names": ["OCD", "OCPD", "compulsive disorder", "compulsive disorders", "compulsive; disorder", "Anankastic Personality", "anancastic personality", "anankastic personality", "Anankastic personality", "Anancastic personality", "Obsessional personality", "obsessional personality", "Compulsive behavior disorder", "compulsive disorder behavior", "compulsive disorder personality", "anankastic personality disorder", "personality disorder; obsessive", "compulsive personality disorder", "Anancastic personality disorder", "Compulsive Personality Disorder", "Compulsive personality disorder", "Anankastic personality disorder", "personality disorder; anankastic", "Compulsive Personality Disorders", "Obsessive-compulsive personality", "OBSESSIVE-COMPULSIVE PERSONALITY", "anankastic; personality disorder", "obsessive compulsive personality", "personality disorder; compulsive", "Obsessional personality disorder", "Disorder, Compulsive Personality", "Obsessive-Compulsive Personality", "compulsive; personality disorder", "obsessive-compulsive personality", "compulsive personality disorders", "Obsessive Compulsive Personality", "Personality Disorder, Compulsive", "Anankastic personality (disorder)", "Personality, Obsessive-Compulsive", "Personality Disorders, Compulsive", "Compulsive personality (disorder)", "Disorders, Compulsive Personality", "Obsessive-Compulsive Personalities", "Obsessional personality (disorder)", "Personalities, Obsessive-Compulsive", "Obsessive-compulsive personality trait", "Obsessive-Compulsive Personality Disorder", "Obsessive compulsive personality disorder", "obsessive compulsive personality disorder", "obsessive-compulsive personality disorder", "PERSONALITY DISORDER OBSESSIVE COMPULSIVE", "Obsessive-compulsive personality disorder", "Obsessive Compulsive Personality Disorder", "Compulsive personality disorder (disorder)", "compulsive personality disorder (diagnosis)", "Obsessive-compulsive personality trait (finding)", "Obsessive compulsive personality disorder (disorder)", "obsessive compulsive personality disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "obsessive-compulsive personality disorder", "shortest_name_length": 3}
{"curie": "MONDO:0002955", "names": ["Vulvar Basal Cell Cancer", "vulvar basal cell cancer", "vulva basal cell carcinoma", "Vulvar Basal Cell Carcinoma", "Vulvar basal cell carcinoma", "vulvar basal cell carcinoma", "basal cell carcinoma of vulva", "Basal Cell Carcinoma of Vulva", "Basal cell carcinoma of Vulva", "Basal cell carcinoma of vulva", "Basal Cell Carcinoma of the Vulva", "basal cell carcinoma of the vulva", "Basal cell carcinoma of vulva (disorder)", "basal cell carcinoma of vulva (diagnosis)", "mammalian vulva skin basal cell carcinoma", "skin basal cell carcinoma of mammalian vulva"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulva basal cell carcinoma", "shortest_name_length": 24}
{"curie": "MONDO:0011981", "names": ["AITD2", "autoimmune thyroid disease, susceptibility to, 2", "AUTOIMMUNE THYROID DISEASE, SUSCEPTIBILITY TO, 2", "autoimmune thyroid disease, susceptibility to, type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune thyroid disease, susceptibility to, 2", "shortest_name_length": 5}
{"curie": "MONDO:0015734", "names": ["rectal duplication", "Rectal duplication", "Congenital duplication of rectum", "Congenital duplication of rectum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rectal duplication", "shortest_name_length": 18}
{"curie": "UMLS:C3899402", "names": ["Decreased Uncorrected Visual Acuity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Decreased Uncorrected Visual Acuity", "shortest_name_length": 35}
{"curie": "MONDO:0022444", "names": ["amyloidosis bronchopulmonary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyloidosis bronchopulmonary", "shortest_name_length": 28}
{"curie": "MONDO:0013982", "names": ["HED", "ECTD11A", "ectodermal dysplasia 11A", "ECTODERMAL DYSPLASIA, HYPOHIDROTIC, AUTOSOMAL DOMINANT", "ectodermal dysplasia, hypohidrotic, autosomal dominant", "ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant", "ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant", "shortest_name_length": 3}
{"curie": "MONDO:0010541", "names": ["Thick calvarial bones", "Calvarial hyperostosis", "calvarial hyperostosis", "Overgrowth of skullcap", "CALVARIAL HYPEROSTOSIS", "Overgrowth of calvarial bones", "Enlargement of calvarial bones", "Hypertrophy of calvarial bones", "X-linked calvarial hyperostosis", "Hyperostosis of calvarial bones", "Excessive growth of calvarial bones", "isolated hyperostosis of the calvarium", "Isolated hyperostosis of the calvarium", "Increased ossification of calvarial bones"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked calvarial hyperostosis", "shortest_name_length": 21}
{"curie": "UMLS:C0855213", "names": ["Stage I Testicular Yolk Sac Tumor", "Testicular yolk sac tumor stage I", "Testicular yolk sac tumour stage I", "Stage I Testicular Yolk Sac Tumor AJCC v6", "Testicular endodermal sinus tumor stage I", "Stage I Testicular Yolk Sac Tumor AJCC v7", "Testicular endodermal sinus tumour stage I", "Stage I Testicular Yolk Sac Tumor AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular yolk sac tumor stage I", "shortest_name_length": 33}
{"curie": "UMLS:C0334366", "names": ["Borderline Papillary Mucinous Cystadenoma", "Borderline Papillary Pseudomucinous Cystadenoma", "Papillary Mucinous Tumor of Low Malignant Potential", "Papillary mucinous tumor of low malignant potential", "Borderline Malignancy Papillary Mucinous Cystadenoma", "Papillary mucinous tumour of low malignant potential", "Papillary mucinous cystadenoma, borderline malignancy", "Papillary mucinous cystadenoma - borderline malignancy", "tumor; papillary, mucinous, of low malignant potential", "Papillary Mucinous Neoplasm of Low Malignant Potential", "papillary; tumor, mucinous, of low malignant potential", "Low Malignancy Potential Papillary Mucinous Cystadenoma", "Borderline Malignancy Papillary Pseudomucinous Cystadenoma", "Papillary pseudomucinous cystadenoma, borderline malignancy", "Low Malignancy Potential Papillary Pseudomucinous Cystadenoma", "Papillary mucinous cystadenoma, borderline malignancy (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Papillary mucinous cystadenoma, borderline malignancy", "shortest_name_length": 41}
{"curie": "MONDO:0012123", "names": ["CDGIe", "CDG1E", "CDG Ie", "CDG 1E", "CDG-Ie", "DPM1-CDG", "DPM1-CDG (CDG-Ie)", "CDG syndrome type Ie", "Dol-P-mannosyltransferase deficiency", "congenital disorder of glycosylation Ie", "congenital disorder of glycosylation 1e", "DPM1 congenital disorder of glycosylation", "Congenital disorder of glycosylation type 1e", "Congenital Disorder of Glycosylation Type Ie", "congenital disorder of glycosylation type 1E", "congenital disorder of glycosylation type Ie", "congenital disorder of glycosylation type 1e", "Congenital disorder of glycosylation type 1E", "Congenital disorder of glycosylation type Ie", "Congenital Disorder of Glycosylation, Type IE", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ie", "congenital disorder of glycosylation, type Ie", "Dolichol-phosphate-mannose synthase 1 deficiency", "Carbohydrate deficient glycoprotein syndrome type Ie", "carbohydrate-deficient glycoprotein syndrome type 1E", "carbohydrate deficient glycoprotein syndrome type Ie", "Congenital disorder of glycosylation type 1e (disorder)", "congenital disorder of glycosylation type Ie (diagnosis)", "congenital disorder of glycosylation caused by mutation in DPM1", "DPM1-CDG - dolichyl-phosphate mannosyltransferase 1 catalytic subunit congenital disorder of glycosylation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital disorder of glycosylation type 1E", "shortest_name_length": 5}
{"curie": "UMLS:C1332881", "names": ["CNS Hamartoma", "Hamartoma of CNS", "Hamartoma of the CNS", "Central Nervous System Hamartoma", "Hamartoma of Central Nervous System", "Hamartoma of the Central Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Hamartoma", "shortest_name_length": 13}
{"curie": "UMLS:C4521796", "names": ["Stage III Gastric (Stomach) Cancer", "Postneoadjuvant Therapy Stage III Gastric Cancer AJCC v8", "Postneoadjuvant Therapy Stage III Gastric Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postneoadjuvant Therapy Stage III Gastric Cancer AJCC v8", "shortest_name_length": 34}
{"curie": "UMLS:C3640087", "names": ["Heterotaxy, Polysplenia", "Polysplenia heterotaxy syndrome", "Heterotaxy Syndrome with Polysplenia", "Polysplenia heterotaxy syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Polysplenia heterotaxy syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0017619", "names": ["CSID with minimal starch tolerance", "disaccharide intolerance with minimal starch tolerance", "congenital sucrose intolerance with minimal starch tolerance", "congenital sucrase-isomaltase deficiency with minimal starch tolerance", "congenital sucrase-isomaltose malabsorption with minimal starch tolerance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital sucrase-isomaltase deficiency with minimal starch tolerance", "shortest_name_length": 34}
{"curie": "MONDO:0011417", "names": ["HFE3", "hemochromatosis type 3", "Hemochromatosis type 3", "hemochromatosis, type 3", "Hemochromatosis, type 3", "Haemochromatosis type 3", "HEMOCHROMATOSIS, TYPE 3", "TFR2-related hemochromatosis", "TFR2 hereditary hemochromatosis", "Hemochromatosis type 3 (disorder)", "hereditary hemochromatosis caused by mutation in TFR2", "HEMOCHROMATOSIS DUE TO DEFECT IN TRANSFERRIN RECEPTOR 2", "hemochromatosis due to defect in transferrin receptor 2", "Hemochromatosis due to defect in transferrin receptor 2", "TFR2 (transferrin receptor 2 gene) related hemochromatosis", "TFR2 (transferrin receptor 2 gene) related haemochromatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemochromatosis type 3", "shortest_name_length": 4}
{"curie": "MONDO:0013847", "names": ["AUTS14B", "16p11.2 duplication", "proximal dup(16)(p11.2)", "Proximal dup(16)(p11.2)", "16p11.2 microduplication", "Proximal trisomy 16p11.2", "proximal trisomy 16p11.2", "16p11.2 duplication syndrome", "susceptibility to autism, 14B", "autism, susceptibility to, 14B", "AUTISM, SUSCEPTIBILITY TO, 14B", "CHROMOSOME 16p11.2 DUPLICATION SYNDROME", "chromosome 16p11.2 duplication syndrome", "Proximal 16p11.2 microduplication syndrome", "proximal 16p11.2 microduplication syndrome", "Proximal 16p11.2 microduplication syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 16p11.2 duplication syndrome", "shortest_name_length": 7}
{"curie": "MONDO:0003639", "names": ["Lung Hilum Tumor", "lung Hilum tumor", "Hilar Lung Tumor", "lung hilum tumor", "hilar lung tumor", "lung hilus tumor", "Hilar Lung Neoplasm", "hilar lung neoplasm", "lung hilus neoplasm", "tumor of lung hilus", "Lung Hilum Neoplasm", "lung hilum neoplasm", "lung neoplasm - hilus", "neoplasm of lung hilus", "Neoplasm of hilus of lung", "neoplasm of hilus of lung", "lung hilus neoplasm (disease)", "Neoplasm of hilus of lung (disorder)", "Neoplasm of hilus of lung (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung hilum neoplasm", "shortest_name_length": 16}
{"curie": "MONDO:0006882", "names": ["Orchitis", "ORCHITIS", "orchitis", "didymytis", "Orchitides", "testisitis", "Orchititis", "Testiculitis", "Orchitis NOS", "Orchitis, NOS", "testi inflammation", "orchitis (disease)", "testis inflammation", "testes inflammation", "Inflammation;testes", "Orchitis (disorder)", "inflammation testis", "inflammation testes", "orchitis (diagnosis)", "testis; inflammation", "inflammation; testis", "Non-specific orchitis", "inflammation of testis", "Inflammation of testis", "Testicular inflammation", "Inflammation of testicles", "Non-specific orchitis, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orchitis", "shortest_name_length": 8}
{"curie": "UMLS:C0855098", "names": ["stage I small lymphocytic lymphoma", "Stage I Small Lymphocytic Lymphoma", "Small Lymphocytic Lymphoma Stage I", "small lymphocytic lymphoma, stage I", "B-Cell Small Lymphocytic Lymphoma Stage I", "Stage I B-Cell Small Lymphocytic Lymphoma", "B-cell small lymphocytic lymphoma stage I", "Ann Arbor Stage I Small Lymphocytic Lymphoma", "Small lymphocyte B lymphoma (Lukes-Collins Classification) stage I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-cell small lymphocytic lymphoma stage I", "shortest_name_length": 34}
{"curie": "MONDO:0009102", "names": ["diaminopentanuria", "Cystine-Lysinuria", "cystine-lysinuria", "DIAMINOPENTANURIA", "CYSTINE-LYSINURIA", "Diaminopentanuria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diaminopentanuria", "shortest_name_length": 17}
{"curie": "UMLS:C0860038", "names": ["Actinomycotic granuloma", "Actinomycotic Granuloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Actinomycotic granuloma", "shortest_name_length": 23}
{"curie": "MONDO:0010169", "names": ["US2", "USH2A", "USH2A Usher syndrome", "Usher syndrome type 2A", "USH2A Usher syndrome 2a", "Usher syndrome, type 2A", "Usher syndrome type IIA", "Usher Syndrome, Type IIA", "USHER syndrome, type IIA", "USHER SYNDROME, TYPE IIA", "Usher syndrome type 2A (diagnosis)", "Usher syndrome caused by mutation in USH2A", "retinal disease in usher syndrome type IIA, modifier of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Usher syndrome type 2A", "shortest_name_length": 3}
{"curie": "MONDO:0001844", "names": ["uterine corpus myxoid leiomyoma", "Uterine Corpus Myxoid Leiomyoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine corpus myxoid leiomyoma", "shortest_name_length": 31}
{"curie": "MONDO:0036781", "names": ["Benign tumor of axilla", "Benign tumour of axilla", "benign axillary neoplasm", "Benign Axillary Neoplasm", "Benign neoplasm of axilla", "axillary neoplasm, benign", "Benign neoplasm of axilla, NOS", "Benign neoplasm of axilla (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign axillary neoplasm", "shortest_name_length": 22}
{"curie": "MONDO:0017088", "names": ["isolated amyelia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated amyelia", "shortest_name_length": 16}
{"curie": "MONDO:0005747", "names": ["enterovirus", "Enterovirus", "Enterovirus diseases", "enterovirus infection", "Enterovirus infection", "Enterovirus Infection", "Enteroviral infection", "enteroviral infection", "enteroviral infections", "infection, Enterovirus", "enterovirus infections", "Enteroviral infections", "Infection, Enterovirus", "Enterovirus Infections", "Infections, Enterovirus", "infections, Enterovirus", "Enteroviral infection NOS", "Enterovirus infection, NOS", "Disease due to Enterovirus", "disease due to enterovirus", "DISEASES DUE TO ENTEROVIRUS", "Disease caused by Enterovirus", "disease caused by enterovirus", "enterovirus infectious disease", "Enterovirus infectious disease", "Disease due to Enterovirus, NOS", "Enterovirus disease or disorder", "Enterovirus infection (diagnosis)", "Enterovirus infection, unspecified", "Enterovirus caused disease or disorder", "Disease caused by Enterovirus (disorder)", "infection; echovirus, unspecified nature or site", "echovirus; infection, unspecified nature or site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "enterovirus infectious disease", "shortest_name_length": 11}
{"curie": "MONDO:0005731", "names": ["Dipetalonemosis", "Dipetalonemiasis", "DIPETALONEMIASIS", "dipetalonemiasis", "Dipetalonemiases", "Mansonella perstans", "Acanthocheilonemiasis", "Dipetalonema Infection", "Dipetalonema infection", "Infection, Dipetalonema", "infection; Dipetalonema", "Dipetalonema Infections", "Dipetalonema; infection", "Dipetalonema infections", "Infections, Dipetalonema", "Infection by Dipetalonema", "infection by Dipetalonema", "dipetalonemiasis (diagnosis)", "Infection by Dipetalonema, NOS", "Dipetalonema infectious disease", "dipetalonema infectious disease", "Infection caused by Dipetalonema", "Infection by Dipetalonema perstans", "infection by Dipetalonema perstans", "Acanthocheilonema perstans infection", "Mansonella perstans infectious disease", "Mansonella perstans disease or disorder", "Infection caused by Dipetalonema (disorder)", "Mansonella perstans caused disease or disorder", "infection by Dipetalonema perstans (disorder) [ambiguous]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dipetalonemiasis", "shortest_name_length": 15}
{"curie": "MONDO:0018624", "names": ["spontaneous cerebrospinal fluid leak", "spontaneous intracranial hypotension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spontaneous intracranial hypotension", "shortest_name_length": 36}
{"curie": "MONDO:0033839", "names": ["osteoradionecrosis of the mandible"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteoradionecrosis of the mandible", "shortest_name_length": 34}
{"curie": "UMLS:C4683742", "names": ["Stage II Mycosis Fungoides and Sezary Syndrome AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Mycosis Fungoides and Sezary Syndrome AJCC v8", "shortest_name_length": 54}
{"curie": "MONDO:0001381", "names": ["bladder lymphoma", "Bladder Lymphoma", "Lymphoma of Bladder", "lymphoma of bladder", "lymphoma of the bladder", "Lymphoma of the Bladder", "urinary bladder lymphoma", "primary bladder lymphoma", "Urinary Bladder Lymphoma", "Primary Bladder Lymphoma", "lymphoma of urinary bladder", "Lymphoma of Urinary Bladder", "lymphoma of the urinary bladder", "Lymphoma of the Urinary Bladder", "Lymphoma of the urinary bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder lymphoma", "shortest_name_length": 16}
{"curie": "MONDO:0014213", "names": ["MRD21", "autosomal dominant mental retardation 21", "mental retardation, autosomal dominant 21", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 21", "autosomal dominant intellectual disability 21", "intellectual disability, autosomal dominant 21", "mental retardation, autosomal dominant type 21", "intellectual disability, autosomal dominant type 21", "autosomal dominant intellectual developmental disorder 21", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 21", "autosomal dominant non-syndromic intellectual disability 21", "intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C4521876", "names": ["Stage IIA", "Stage IIA Pancreatic Cancer", "Stage IIA Pancreatic Cancer AJCC v8", "Stage IIA Exocrine Pancreatic Cancer AJCC v8", "Stage IIA Exocrine Pancreatic Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Pancreatic Cancer AJCC v8", "shortest_name_length": 9}
{"curie": "MONDO:0002473", "names": ["Renal Cyst", "Cyst;renal", "renal cyst", "RENAL CYST", "Renal cyst", "renal Cyst", "Kidney cyst", "kidney cyst", "cyst; renal", "renal; cyst", "Kidney Cyst", "KIDNEY CYST", "Renal cysts", "kidney; cyst", "cyst; kidney", "Kidney Cysts", "Kidney cysts", "Cystic Kidney", "Cystic kidney", "cystic kidney", "kidney cystic", "Cystic Kidneys", "kidney; cystic", "Cyst of kidney", "cystic; kidney", "Cyst of Kidney", "Renal cyst NOS", "Kidney, Cystic", "cyst of kidney", "cystic kidneys", "Cystic kidneys", "Kidneys, Cystic", "Cyst of the Kidney", "Cystic Renal Disease", "renal cystic disease", "RENAL CYSTIC DISEASE", "cystic renal disease", "Cystic renal disease", "Cystic Renal Diseases", "Cystic Kidney Disease", "Disease, Cystic Renal", "Renal Disease, Cystic", "Cystic kidney disease", "cystic diseases renal", "cystic kidney disease", "Disease, Cystic Kidney", "cystic diseases kidney", "Diseases, Cystic Renal", "renal cyst (diagnosis)", "Cystic Kidney Diseases", "Renal Diseases, Cystic", "Kidney Disease, Cystic", "Kidney Diseases, Cystic", "Diseases, Cystic Kidney", "Cystic disease of kidney", "Cyst of kidney (disorder)", "Renal cyst (excl congenital)", "Renal cyst (excluding congenital)", "cystic kidney disease (diagnosis)", "Cystic kidney disease, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cystic kidney disease", "shortest_name_length": 10}
{"curie": "MONDO:0012136", "names": ["CPT2, neonatal form", "CPTII, neonatal form", "CPT2, lethal systemic form", "CPTII, lethal systemic form", "Cpt2 deficiency, lethal neonatal", "CPT2 Deficiency, Lethal Neonatal", "CPT2 DEFICIENCY, LETHAL NEONATAL", "CPT 2 deficiency, lethal neonatal", "CPT II Deficiency, Lethal Neonatal", "CPT II DEFICIENCY, LETHAL NEONATAL", "CPT II deficiency, lethal neonatal", "Carnitine Palmitoyltransferase 2 deficiency, neonatal", "CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL", "Carnitine Palmitoyltransferase 2 deficiency, antenatal", "Carnitine Palmitoyltransferase II Deficiency, Neonatal", "Carnitine Palmitoyltransferase II Deficiency, Antenatal", "CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL", "Carnitine palmitoyl transferase II deficiency, neonatal form", "carnitine palmitoyl transferase II deficiency, neonatal form", "Carnitine Palmitoyltransferase 2 deficiency, lethal neonatal", "CARNITINE PALMITOYLTRANSFERASE II deficiency, lethal neonatal", "CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL", "Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal", "Carnitine palmitoyl transferase deficiency type 2, neonatal form", "Carnitine palmitoyl transferase II deficiency, lethal systemic form", "Carnitine palmitoyl transferase deficiency type 2, lethal systemic form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carnitine palmitoyl transferase II deficiency, neonatal form", "shortest_name_length": 19}
{"curie": "MONDO:0021465", "names": ["Benign Appendix Tumor", "benign appendix tumor", "benign appendix neoplasm", "Benign Appendix Neoplasm", "Benign tumor of appendix", "benign tumor of appendix", "Benign Tumor of Appendix", "Benign tumour of appendix", "Benign Neoplasm of Appendix", "Benign neoplasm of appendix", "benign appendiceal neoplasm", "benign neoplasm of appendix", "Benign Tumor of the Appendix", "benign tumor of the appendix", "Benign Neoplasm of the Appendix", "benign neoplasm of the appendix", "vermiform appendix benign neoplasm", "Benign neoplasm of appendix (disorder)", "benign neoplasm of appendix (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of appendix", "shortest_name_length": 21}
{"curie": "MONDO:0011622", "names": ["UAN", "UROLITHIASIS, URIC ACID, SUSCEPTIBILITY TO", "urolithiasis, uric acid, susceptibility to", "susceptibility to uric acid nephrolithiasis", "URIC ACID NEPHROLITHIASIS, SUSCEPTIBILITY TO", "nephrolithiasis, uric acid, susceptibility to", "NEPHROLITHIASIS, URIC ACID, SUSCEPTIBILITY TO", "NEPHROLITHIASIS, URIC ACID, SUSCEPTIBILITY TO (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrolithiasis, uric acid, susceptibility to", "shortest_name_length": 3}
{"curie": "UMLS:C0751812", "names": ["Post-Concussive Coma", "Coma, Post Concussive", "Coma, Post-Concussive", "Post-Concussive Comas", "Comas, Post-Concussive", "Coma, Post-Traumatic, Prolonged"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Coma, Post-Traumatic, Prolonged", "shortest_name_length": 20}
{"curie": "UMLS:C0236072", "names": ["bronchospasm paradoxical", "Bronchospasm paradoxical", "BRONCHOSPASM PARADOXICAL", "paradoxical bronchospasm", "Paradoxical bronchospasm", "Paradoxical bronchospasm (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paradoxical bronchospasm", "shortest_name_length": 24}
{"curie": "MONDO:0010253", "names": ["MFTS", "Mfts", "MGR2", "Mgr2", "migraine, familial typical, susceptibility to, 2", "migraine with or without aura, susceptibility to, 2", "MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 2", "migraine, familial typical, susceptibility to, type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "migraine, familial typical, susceptibility to, 2", "shortest_name_length": 4}
{"curie": "MONDO:0025512", "names": ["type II hypersensitivity disease", "disorder of type II hypersensitivity", "type II hypersensitivity reaction disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type II hypersensitivity reaction disease", "shortest_name_length": 32}
{"curie": "UMLS:C1136210", "names": ["Meningococcal Meningitis, Serogroup W135", "Serogroup W135, Meningococcal Meningitis", "Meningitis, Meningococcal, Serogroup W135", "Meningococcal Meningitis, Serogroup W-135", "Serogroup W-135, Meningococcal Meningitis", "Serogroup W 135, Meningococcal Meningitis", "Meningococcal Meningitis, Serogroup W 135", "Meningitis, Meningococcal, Serogroup W-135"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meningitis, Meningococcal, Serogroup W-135", "shortest_name_length": 40}
{"curie": "MONDO:0015327", "names": ["developmental anomaly of metabolic origin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental anomaly of metabolic origin", "shortest_name_length": 41}
{"curie": "MONDO:0002996", "names": ["cavernous sinus meningioma", "Cavernous Sinus Meningioma", "meningioma of cavernous sinus", "Meningioma of Cavernous Sinus", "Meningioma of the Cavernous Sinus", "meningioma of the Cavernous sinus", "meningioma of the cavernous sinus", "cavernous sinus meningioma (disease)", "meningioma (disease) of cavernous sinus", "meningioma of cavernous sinus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cavernous sinus meningioma", "shortest_name_length": 26}
{"curie": "UMLS:C0862780", "names": ["Stage IIIB Adenosquamous Lung Cancer", "Stage IIIB Adenosquamous Lung Carcinoma", "Adenosquamous cell lung cancer stage IIIB", "Stage IIIB Adenosquamous Cell Lung Carcinoma", "Stage IIIB Lung Adenosquamous Carcinoma AJCC v7", "Stage IIIB Adenosquamous Cell Carcinoma of Lung", "Stage IIIB Adenosquamous Cell Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenosquamous cell lung cancer stage IIIB", "shortest_name_length": 36}
{"curie": "MONDO:0014280", "names": ["CD3D", "IMD19", "CD3delta deficiency", "immunodeficiency 19", "IMMUNODEFICIENCY 19", "CD3-delta deficiency", "CD3-DELTA DEFICIENCY", "CD3-Delta deficiency", "immunodeficiency type 19", "CD3D severe combined immunodeficiency (disease)", "SCID T cell-negative, B cell-positive, NK cell-positive", "SCID, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-POSITIVE", "SCID, T cell-negative, B cell-positive, NK cell-positive", "severe combined immunodeficiency (disease) caused by mutation in CD3D", "severe combined immunodeficiency, T cell-negative, B cell-positive, NK cell-positive", "SEVERE COMBINED IMMUNODEFICIENCY, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-POSITIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 19", "shortest_name_length": 4}
{"curie": "UMLS:C4525200", "names": ["Stage I Hepatocellular Cancer", "Stage I Liver Cell Carcinoma AJCC v8", "Stage I Hepatocellular Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Hepatocellular Carcinoma AJCC v8", "shortest_name_length": 29}
{"curie": "MONDO:0007359", "names": ["Commissural pit", "Commissural lip pit", "COMMISSURAL LIP PITS", "Commissural lip pits", "commissural lip pits", "Commissural labial pits", "Congenital commissural pits", "Pits at the corners of the lips", "Lip pits at corners of the mouth", "Congenital commissural pits (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "commissural lip pits", "shortest_name_length": 15}
{"curie": "MONDO:0019200", "names": ["RP", "rp", "rod cone dystrophy", "Rod Cone Dystrophy", "rod-cone dystrophy", "Rod-Cone Dystrophy", "Rod cone dystrophy", "Rod-cone dystrophy", "cone rod dystrophy", "Retinitis pigmentosa", "Rod-Cone Dystrophies", "RETINITIS PIGMENTOSA", "retinitis pigmentosa", "Retinitis;pigmentosa", "Retinitis Pigmentosa", "Rod Cone Dystrophies", "retinitis; pigmentosa", "pigmentosa; retinitis", "pigmentary retinopathy", "Pigmentary Retinopathy", "Retinopathy, Pigmentary", "Pigmentary Retinopathies", "Retinopathies, Pigmentary", "RP - Retinitis pigmentosa", "Retinitis pigmentosa (RP)", "Tapetoretinal Degeneration", "Tapetoretinal degeneration", "Rod-cone retinal dystrophy", "tapetoretinal; degeneration", "degeneration; tapetoretinal", "Tapetoretinal Degenerations", "CHORIORETINAL HEREDODYSTROPHY", "Retinitis pigmentosa (disorder)", "retinitis pigmentosa (diagnosis)", "pericentral pigmentary retinopathy", "DYSTROPHY, PERIPHERAL TAPETORETINAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa", "shortest_name_length": 2}
{"curie": "MONDO:0012931", "names": ["FSGS4", "APOL1 focal segmental glomerulosclerosis", "susceptibility to focal segmental glomerulosclerosis 4", "FOCAL SEGMENTAL GLOMERULOSCLEROSIS 4, SUSCEPTIBILITY TO", "focal segmental glomerulosclerosis 4, susceptibility to", "end-stage renal disease, nondiabetic, susceptibility to", "glomerulosclerosis, focal segmental, 4, susceptibility to", "focal segmental glomerulosclerosis caused by mutation in APOL1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal segmental glomerulosclerosis 4, susceptibility to", "shortest_name_length": 5}
{"curie": "MONDO:0009817", "names": ["OPTB5", "OSTM1 osteopetrosis (disease)", "autosomal recessive osteopetrosis 5", "osteopetrosis autosomal recessive 5", "infantile malignant osteopetrosis 3", "osteopetrosis infantile malignant 3", "Osteopetrosis, Autosomal Recessive 5", "osteopetrosis, autosomal recessive 5", "OSTEOPETROSIS, AUTOSOMAL RECESSIVE 5", "OSTEOPETROSIS, INFANTILE MALIGNANT 3", "Osteopetrosis, Infantile Malignant 3", "osteopetrosis, infantile malignant 3", "autosomal recessive osteopetrosis type 5", "osteopetrosis, autosomal recessive type 5", "osteopetrosis (disease) caused by mutation in OSTM1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive osteopetrosis 5", "shortest_name_length": 5}
{"curie": "UMLS:C0025060", "names": ["Mediastinal Cyst", "Mediastinal cyst", "mediastinal cyst", "Mediastinal Cysts", "Cyst, Mediastinal", "Cysts, Mediastinal", "Cyst of mediastinum", "Cyst of Mediastinum", "Cyst of the Mediastinum", "Cyst of mediastinum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mediastinal Cyst", "shortest_name_length": 16}
{"curie": "MONDO:0005961", "names": ["SINUSITIS", "sinusitis", "Sinusitis", "Highmoritis", "Sinusitides", "Sinus disease", "Sinusitis NOS", "Sinusitis, NOS", "Sinus Infection", "infected; sinus", "sinus infection", "sinus; infected", "SINUS INFECTION", "Sinus infection", "sinus; infection", "infection; sinus", "Infection, Sinus", "Sinus Infections", "Infections, Sinus", "Sinus inflammation", "inflammation; sinus", "sinus; inflammation", "Sinusitis (disorder)", "Unspecified sinusitis", "sinusitis (diagnosis)", "nasal sinus; inflammation", "inflammation; nasal sinus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sinusitis", "shortest_name_length": 9}
{"curie": "UMLS:C0279067", "names": ["Grade III LYG", "Grade III Lymphomatoid Granulomatosis", "Angiocentric immunoproliferative lesion grade 3", "Grade III Angiocentric Immunoproliferative Lesion", "Angiocentric Immunoproliferative Lesion Grade III", "Grade III Angiocentric Immunoproliferative Lesions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade III Lymphomatoid Granulomatosis", "shortest_name_length": 13}
{"curie": "UMLS:C0041428", "names": ["conjoin twin", "siamese twin", "TWIN SIAMESE", "Siamese Twin", "Siamese Twins", "Siamese twins", "twins siamese", "siamese twins", "Twin, Siamese", "twins; fusion", "fusion; twins", "Twins, Siamese", "Conjoined Twin", "conjoined twin", "conjoined twins", "twins conjoined", "CONJOINED TWINS", "Conjoined Twins", "twin; conjoined", "Twin, Conjoined", "Conjoined twins", "conjoining twins", "Twins, Conjoined", "Siamese twins, NOS", "Conjoined twins, NOS", "Conjoined twins (disorder)", "conjoined twins (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Twins, Conjoined", "shortest_name_length": 12}
{"curie": "UMLS:C3544180", "names": ["Accidental exposure to product by child"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Accidental exposure to product by child", "shortest_name_length": 39}
{"curie": "MONDO:0001268", "names": ["Gum recession", "Receding Gums", "Receding gums", "Receding gingiva", "gingival recession", "Exposed tooth neck", "GINGIVAL RECESSION", "Gingival Recession", "Gingival recession", "recession; gingival", "gingival; recession", "gingival recessions", "Recession, Gingival", "Gingival recessions", "Gingival Recessions", "Recessions, Gingival", "Gingival recession, NOS", "severe gingival recession", "minimal gingival recession", "moderate gingival recession", "localized gingival recession", "Localized gingival recession", "Localised gingival recession", "Gingival recession (disorder)", "gingival recession, localized", "Gingival recession, localized", "gingival recession (diagnosis)", "Gingival soft tissue recession", "Gingival recession, unspecified", "gingival recession, unspecified", "Localized gingival recession, NOS", "gingival recession (physical finding)", "Localized gingival recession (disorder)", "localized gingival recession (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gingival recession", "shortest_name_length": 13}
{"curie": "OMIM:112050", "names": [], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"]}
{"curie": "UMLS:C0154724", "names": ["Cerebral Cyst", "cerebral cyst", "Cerebral cyst", "cerebral cysts", "Cerebral cysts", "Cyst of Cerebrum", "Cerebral cyst NOS", "Cerebral cyst, NOS", "Intracerebral cyst", "Intracerebral cysts", "Cyst of the Cerebrum", "Cerebral cyst (disorder)", "Cerebral Hemispheric Cyst", "cerebral cyst (diagnosis)", "Cyst of Cerebral Hemispheres", "Cyst of the Cerebral Hemispheres"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebral cyst", "shortest_name_length": 13}
{"curie": "MONDO:0007235", "names": ["BOFS", "BOF SYNDROME", "Bof syndrome", "BOF Syndrome", "BOFS syndrome", "Syndrome, BOF", "Lee Root Fenske Syndrome", "BRANCHIOOCULOFACIAL SYNDROME", "Branchiooculofacial Syndrome", "branchiooculofacial syndrome", "Branchiooculofacial syndrome", "branchio-oculo-facial syndrome", "branchio oculo facial syndrome", "Branchio-Oculo-Facial Syndrome", "Branchio-oculo-facial syndrome", "Branchio Oculo Facial Syndrome", "Branchiooculofacial syndrome (disorder)", "branchial clefts-lip pseudocleft syndrome", "branchio-oculo-facial (BOF) syndrome (BOFS)", "Lip Pseudocleft-Hemangiomatous Branchial Cyst Syndrome", "LIP PSEUDOCLEFT-HEMANGIOMATOUS BRANCHIAL CYST SYNDROME", "lip pseudocleft-hemangiomatous branchial cyst syndrome", "lip Pseudocleft-Hemangiomatous branchial cyst syndrome", "Lip Pseudocleft Hemangiomatous Branchial Cyst Syndrome", "hemangiomatous branchial clefts-Lip Pseudocleft syndrome", "Hemangiomatous Branchial Clefts-Lip Pseudocleft Syndrome", "HEMANGIOMATOUS BRANCHIAL CLEFTS-LIP PSEUDOCLEFT SYNDROME", "Hemangiomatous Branchial Clefts Lip Pseudocleft Syndrome", "hemangiomatous branchial clefts-lip pseudocleft syndrome", "branchial clefts with characteristic facies growth retardation imperforate nasolacrimal duct and premature aging", "branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and premature Aging", "Branchial Clefts with Characteristic Facies, Growth Retardation, Imperforate Nasolacrimal Duct, and Premature Aging", "BRANCHIAL CLEFTS WITH CHARACTERISTIC FACIES, GROWTH RETARDATION, IMPERFORATE NASOLACRIMAL DUCT, AND PREMATURE AGING"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "branchiooculofacial syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0001422", "names": ["Conn", "Conn syndrome", "Conn Syndrome", "conn syndrome", "CONN SYNDROME", "Syndrome, Conn", "conns syndrome", "Conns Syndrome", "Conn's Syndrome", "conn's syndrome", "Conn's syndrome", "Syndrome, Conn's", "primary aldosteronism", "Primary aldosteronism", "Aldosteronism Primary", "ALDOSTERONISM, PRIMARY", "Idiopathic aldosteronism", "Primary Hyperaldosteronism", "Primary hyperaldosteronism", "PRIMARY HYPERALDOSTERONISM", "primary hyperaldosteronism", "hyperaldosteronism; primary", "Hyperaldosteronism, Primary", "Hyperaldosteronism, primary", "primary; hyperaldosteronism", "HYPERALDOSTERONISM, PRIMARY", "Conn's syndrome (diagnosis)", "Idiopathic hyperaldosteronism", "primary aldosteronism (diagnosis)", "Idiopathic aldosteronism (disorder)", "Primary hyperaldosteronism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary aldosteronism", "shortest_name_length": 4}
{"curie": "UMLS:C1709312", "names": ["Papillary carcinoma, oxyphilic cell", "Oncocytic Variant Thyroid Gland Papillary Cancer", "Oxyphilic Variant Thyroid Gland Papillary Carcinoma", "Oncocytic Variant Thyroid Gland Papillary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oncocytic Variant Thyroid Gland Papillary Carcinoma", "shortest_name_length": 35}
{"curie": "MONDO:0018494", "names": ["microcephaly-short stature-intellectual disability-facial dysmorphism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly-short stature-intellectual disability-facial dysmorphism syndrome", "shortest_name_length": 78}
{"curie": "MONDO:0007514", "names": ["ECTOL1", "Ectopia lentis isolated", "Ectopia lentis syndrome", "Isolated ectopia lentis", "Familial ectopia lentis", "Ectopia Lentis, Isolated", "ectopia lentis, familial", "FBN1 isolated ectopia lentis", "autosomal dominant isolated ectopia lentis 1", "ectopia lentis 1, isolated, autosomal dominant", "ECTOPIA LENTIS 1, ISOLATED, AUTOSOMAL DOMINANT", "isolated ectopia lentis caused by mutation in FBN1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectopia lentis 1, isolated, autosomal dominant", "shortest_name_length": 6}
{"curie": "MONDO:0007784", "names": ["PRTH", "RTHb", "Resistance to thyroid hormone beta", "pituitary resistance to thyroid hormone", "selective pituitary thyroid hormone resistance", "THYROID HORMONE RESISTANCE, SELECTIVE PITUITARY", "thyroid hormone resistance, selective pituitary", "Thyroid Hormone Resistance, Selective Pituitary", "selective pituitary resistance to thyroid hormone", "Resistance to thyroid hormone due to a mutation in TRb", "familial hyperthyroidism due to inappropriate thyrotropin secretion", "hyperthyroidism, familial, due to inappropriate thyrotropin secretion", "Hyperthyroidism, Familial, due to Inappropriate Thyrotropin Secretion", "HYPERTHYROIDISM, FAMILIAL, DUE TO INAPPROPRIATE THYROTROPIN SECRETION", "Resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "selective pituitary resistance to thyroid hormone", "shortest_name_length": 4}
{"curie": "MONDO:0004196", "names": ["Rectal Sarcomatoid Cancer", "rectal sarcomatoid cancer", "Rectal Sarcomatoid Carcinoma", "rectal sarcomatoid carcinoma", "rectum sarcomatoid carcinoma", "rectal spindle cell carcinoma", "Rectal Spindle Cell Carcinoma", "sarcomatoid carcinoma of rectum", "Sarcomatoid Carcinoma of Rectum", "Sarcomatoid Carcinoma of the Rectum", "sarcomatoid carcinoma of the rectum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rectal sarcomatoid carcinoma", "shortest_name_length": 25}
{"curie": "UMLS:C5420001", "names": ["Refractory Indolent Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Indolent Non-Hodgkin Lymphoma", "shortest_name_length": 40}
{"curie": "MONDO:0100398", "names": ["AML, inv(3)(q21q26.2)", "AML, inv(3)(q21.3q26.2)", "AML, inv(3)(q21.3;q26.2)", "acute myeloid leukemia, inv(3)(q21.3;q26.2)", "Acute Myeloid Leukemia with inv(3)(q21q26.2); RPN1-EVI1", "Acute Myeloid Leukemia with inv(3) (q21.3;q26.2); GATA2, MECOM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, inv(3)(q21.3;q26.2)", "shortest_name_length": 21}
{"curie": "MONDO:0010476", "names": ["BPAN", "NBIA5", "SENDA", "NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5", "Neurodegeneration with Brain Iron Accumulation 5", "neurodegeneration with brain iron accululation 5", "neurodegeneration with brain iron accumulation 5", "Beta-propeller Protein-associated Neurodegeneration", "beta-propeller protein-associated neurodegeneration", "Beta-Propeller Protein-Associated Neurodegeneration", "BETA-PROPELLER PROTEIN-ASSOCIATED NEURODEGENERATION", "Beta-propeller protein-associated neurodegeneration", "WDR45 neurodegeneration with brain iron accumulation", "Neurodegeneration with brain iron accumulation type 5", "neurodegeneration with brain iron accumulation type 5", "BPAN - beta-propeller protein-associated neurodegeneration", "Beta-propeller protein-associated neurodegeneration (disorder)", "neurodegeneration with brain iron accumulation 5, X-linked dominant", "static encephalopathy of childhood with neurdegeneration in adulthood", "Static encephalopathy of childhood with neurodegeneration in adulthood", "static encephalopathy Of childhood with neurodegeneration In adulthood", "Static Encephalopathy Of Childhood With Neurodegeneration In Adulthood", "STATIC ENCEPHALOPATHY OF CHILDHOOD WITH NEURODEGENERATION IN ADULTHOOD", "static encephalopathy of childhood with neurodegeneration in adulthood", "neurodegeneration with brain iron accumulation caused by mutation in WDR45"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodegeneration with brain iron accumulation 5", "shortest_name_length": 4}
{"curie": "UMLS:C0267091", "names": ["Aorto-esophageal fistula", "Aorto-oesophageal fistula", "Aorto-esophageal fistula (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aorto-esophageal fistula", "shortest_name_length": 24}
{"curie": "MONDO:0002547", "names": ["tumor nerve sheath", "sheath nerve tumor", "nerve sheath tumor", "Nerve Sheath Tumor", "Nerve sheath tumor", "Nerve Sheath Tumors", "Tumor, Nerve Sheath", "Sheath Tumor, Nerve", "NERVE SHEATH TUMORS", "nerve sheath tumour", "nerve sheath tumors", "Nerve sheath tumour", "Sheath Tumors, Nerve", "Tumors, Nerve Sheath", "tumor of nerve sheath", "nerve sheath neoplasm", "Nerve Sheath Neoplasm", "Tumor of Nerve Sheath", "Nerve Sheath Neoplasms", "Neoplasm, Nerve Sheath", "nerve sheath neoplasms", "Neoplasms, Nerve Sheath", "neoplasm of nerve sheath", "Neoplasm of Nerve Sheath", "Tumors of the Nerve Sheath", "neoplasm of the nerve Sheath", "neoplasm of the nerve sheath", "Neoplasm of the Nerve Sheath", "Peripheral nerve sheath tumor", "Peripheral Nerve Sheath Tumor", "peripheral nerve sheath tumor", "peripheral nerve sheath tumors", "Peripheral Nerve Sheath Tumors", "Nerve Sheath Tumors, Peripheral", "peripheral nerve sheath neoplasm", "Peripheral Nerve Sheath Neoplasm", "Peripheral nerve sheath tumor (disorder)", "Nerve sheath tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nerve sheath neoplasm", "shortest_name_length": 18}
{"curie": "MONDO:0011673", "names": ["DFNA30", "autosomal dominant deafness 30", "DEAFNESS, AUTOSOMAL DOMINANT 30", "Deafness, Autosomal Dominant 30", "deafness, autosomal dominant 30", "autosomal dominant nonsyndromic deafness 30", "autosomal dominant nonsyndromic hearing loss 30", "autosomal dominant nonsyndromic deafness type 30"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 30", "shortest_name_length": 6}
{"curie": "MONDO:0013165", "names": ["SPG45", "SPG65", "hereditary spastic paraplegia 45", "hereditary spastic paraplegia type 45", "autosomal recessive spastic paraplegia 45", "SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE", "spastic paraplegia 45, autosomal recessive", "Autosomal recessive spastic paraplegia type 65", "autosomal recessive spastic paraplegia type 45", "autosomal recessive spastic paraplegia type 65", "Autosomal recessive spastic paraplegia type 45", "NT5C2 autosomal recessive complex spastic paraplegia", "familial spastic paraplegia autosomal recessive type 45", "Autosomal recessive spastic paraplegia type 45 (disorder)", "Autosomal recessive spastic paraplegia type 45 (diagnosis)", "autosomal recessive complex spastic paraplegia caused by mutation in NT5C2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 45", "shortest_name_length": 5}
{"curie": "MONDO:0018994", "names": ["CMTX", "COWCK", "Charcot-Marie-Tooth disease type X", "X-linked Charcot-Marie-Tooth disease", "X-linked hereditary motor and sensory neuropathy", "X-linked hereditary motor and sensory neuropathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type X", "shortest_name_length": 4}
{"curie": "MONDO:0010702", "names": ["OFD1", "OFDI", "OFDSI", "OFDS I", "OFDS 1", "OFD syndrome 1", "Gorlin syndrome 1", "OFD syndrome type I", "Gorlin Psaume Syndrome", "Gorlin-Psaume syndrome", "Gorlin-Psaume Syndrome", "Papillon-Leage syndrome", "Syndrome, Gorlin-Psaume", "dysplasia linguofacialis", "orodigitofacial syndrome", "orofaciodigital syndrome 1", "orodigitofacial dysostosis", "OROFACIODIGITAL SYNDROME I", "orofaciodigital syndrome I", "Orofaciodigital Syndrome I", "digito-orofacial syndrome I", "Orofaciodigital Syndrome Is", "Orofacial-digital syndrome I", "Oral-facial-digital syndrome", "oral-facial-digital syndrome I", "Orofaciodigital syndrome type1", "oral facial digital syndrome 1", "Papillon Léage Psaume syndrome", "oral-facial-digital syndrome 1", "Papillon-Leage-Psaume syndrome", "Papillon-Léage-Psaume syndrome", "Orofaciodigital Syndrome Type 1", "Orofaciodigital syndrome type 1", "orofaciodigital syndrome type I", "orofaciodigital syndrome type 1", "Papillon-League-Psaume syndrome", "orofaciodigital (OFD) syndrome I", "Papillon-Leage and Psaume syndrome", "PAPILLON-LEAGE AND PSAUME SYNDROME", "Papillon-Leage and Psaume Syndrome", "Oro-facial digital syndrome type 1", "Papillon Leage and Psaume Syndrome", "Oral-facial-digital syndrome type 1", "oral facial digital syndrome type 1", "oral-facial-digital syndrome type 1", "Oral-facial-digital syndrome, type 1", "Oral Facial Digital Syndrome, Type I", "Oral-Facial-Digital Syndrome, Type I", "ORAL-FACIAL-DIGITAL SYNDROME, TYPE I", "OFD I - Orofacial-digital syndrome I", "oral-facial-digital syndrome, type 1", "Papillon-league-Psaume syndrome (formerly)", "Oro-facial digital syndrome type 1 (disorder)", "orofaciodigital syndrome i, X-linked dominant", "oral-facial-digital syndrome type 1 (diagnosis)", "Facial milia, lobate tongue, lingual and labial frenula syndrome", "Facial milia, lobate tongue, lingual and labial frenula syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orofaciodigital syndrome I", "shortest_name_length": 4}
{"curie": "UMLS:C1336734", "names": ["Thecoma/Fibroma Group Ovarian Tumor", "Ovarian Tumor of the Thecoma/Fibroma Group"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Tumor of the Thecoma/Fibroma Group", "shortest_name_length": 35}
{"curie": "MONDO:0014915", "names": ["SRTD16", "SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY", "short-rib thoracic dysplasia 16 with or without polydactyly", "short-rib thoracic dysplasia 16 with or without polydactyly; SRTD16"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short-rib thoracic dysplasia 16 with or without polydactyly", "shortest_name_length": 6}
{"curie": "UMLS:C0278720", "names": ["Relapsed Retinoblastoma", "Recurrent Retinoblastoma", "recurrent retinoblastoma", "retinoblastoma, recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Retinoblastoma", "shortest_name_length": 23}
{"curie": "UMLS:C1333116", "names": ["Colorectal TSA", "Colorectal Serrated Adenoma", "Colorectal Serrated Adenoma Type II", "Colorectal Traditional Serrated Adenoma", "Large Bowel Traditional Serrated Adenoma", "Traditional Serrated Adenoma of Large Bowel", "Traditional Serrated Adenoma of the Large Bowel"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Traditional Serrated Adenoma", "shortest_name_length": 14}
{"curie": "UMLS:C3899647", "names": ["Childhood Parathyroid Gland Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Parathyroid Gland Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0010993", "names": ["Harrod syndrome", "HARROD SYNDROME", "Harrod Doman Keele syndrome", "Cranio-facio-digito-genital syndrome", "cranio-facio-digito-genital syndrome", "craniofacial digital genital anomalies", "Craniofacial digital genital anomalies", "craniofacial digital and genital anomalies syndrome", "Craniofacial digital and genital anomalies syndrome", "Craniofacial digital and genital anomalies syndrome (disorder)", "craniofacial digital and genital anomalies syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Harrod syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0043370", "names": ["Adrenal supression", "central Hypoadrenalism", "Central Hypoadrenalism", "secondary hypocortisolism", "Secondary hypocortisolism", "central adrenal insufficiency", "Central adrenal insufficiency", "Secondary hypoadrenocorticism", "Central Adrenal Insufficiency", "secondary adrenal insufficiency", "Secondary adrenal insufficiency", "Secondary Adrenal Insufficiency", "secondary adrenocortical insufficiency", "Secondary adrenocortical insufficiency", "secondary adrenal insufficiency (diagnosis)", "Hypocortisolism secondary to another disorder", "hypocortisolism secondary to another disorder", "Hypocortisolism secondary to another disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary adrenal insufficiency", "shortest_name_length": 18}
{"curie": "MONDO:0002974", "names": ["Ca cervix", "cervical ca", "Cervix cancer", "cervix cancer", "Cervix Cancer", "Cancer, Cervix", "Cervical Cancer", "Cervical cancer", "CERVICAL CANCER", "cervical cancer", "Cervical Cancers", "cervical cancers", "cancer of cervix", "Cancer of Cervix", "Cancer of cervix", "Cancer, Cervical", "cervical neoplasm", "cervix uteri cancer", "Cervix uteri--Cancer", "cancer of the cervix", "Cancer of the Cervix", "uterine cervix cancer", "Neoplasm malig;cervix", "Malignant Cervix Tumor", "malignant cervix tumor", "Uterine Cervical Cancer", "Malignant Cervical Tumor", "Cancer, Uterine Cervical", "cervical cancer, somatic", "Uterine Cervical Cancers", "Cervical Cancer, Uterine", "malignant cervical tumor", "cancer of uterine cervix", "Malignant Cervix Neoplasm", "Malignant tumor of cervix", "malignant tumor of cervix", "tumor of the cervix uteri", "Malignant Tumor of Cervix", "uterine cervical neoplasm", "Malignant neoplasm cervix", "malignant cervix neoplasm", "tumor of the Cervix Uteri", "Cervix neoplasms malignant", "Malignant tumour of cervix", "neoplasm of uterine cervix", "malignant cervical neoplasm", "Malignant Cervical Neoplasm", "cervical cancer (diagnosis)", "Malignant Cervix Uteri Tumor", "Cancer of the uterine cervix", "Malignant neoplasm of cervix", "malignant neoplasm of cervix", "malignant cervix uteri tumor", "Cancer of the Uterine Cervix", "Malignant Neoplasm of Cervix", "malignant tumor of the cervix", "Malignant Tumor of the Cervix", "Malignant Uterine Cervix Tumor", "malignant uterine cervix tumor", "malignant cervix uteri neoplasm", "Malignant Tumor of Cervix Uteri", "malignant tumor of cervix uteri", "Malignant Cervix Uteri Neoplasm", "Malignant Neoplasm of the Cervix", "malignant neoplasm of the cervix", "malignant neosplasm of the cervix", "Malignant Uterine Cervix Neoplasm", "malignant uterine cervix neoplasm", "malignant tumor of uterine cervix", "Malignant Tumor of Uterine Cervix", "malignant neoplasm of cervix uteri", "Malignant Neoplasm of Cervix Uteri", "Malignant neoplasm of cervix uteri", "Malignant Tumor of the Cervix Uteri", "malignant tumor of the cervix uteri", "Malignant tumor of cervix (disorder)", "malignant neoplasm of uterine cervix", "Malignant neoplasm of uterine cervix", "Malignant Neoplasm of Uterine Cervix", "Malignant Tumor of the Uterine Cervix", "malignant tumor of the uterine cervix", "malignant neoplasm of the cervix uteri", "Malignant Neoplasm of the Cervix Uteri", "malignant neoplasm of the uterine cervix", "malignant neoplasm of cervix (diagnosis)", "cervical neoplasm malignant cervix uteri", "Malignant Neoplasm of the Uterine Cervix", "malignant neoplasm of cervix uteri (diagnosis)", "Malignant neoplasm of cervix uteri, unspecified", "Malignant neoplasm of cervix uteri, unspecified site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical cancer", "shortest_name_length": 9}
{"curie": "UMLS:C0729549", "names": ["Gastrointestinal fungal infection", "Fungal gastrointestinal infection", "Fungal gastrointestinal infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fungal gastrointestinal infection", "shortest_name_length": 33}
{"curie": "UMLS:C0751744", "names": ["Acquired Metabolic Encephalopathy", "Metabolic Encephalopathy, Acquired", "Acquired Metabolic Diseases, Brain", "Metabolic Brain Syndrome, Acquired", "Encephalopathy, Acquired Metabolic", "Metabolic Brain Diseases, Acquired", "Brain Diseases, Metabolic, Acquired", "Metabolic Brain Syndromes, Acquired", "Brain Syndrome, Metabolic, Acquired", "Acquired Metabolic Encephalopathies", "Encephalopathy, Metabolic, Acquired", "Encephalopathies, Acquired Metabolic", "Metabolic Encephalopathies, Acquired", "Brain Disorders, Metabolic, Acquired"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brain Diseases, Metabolic, Acquired", "shortest_name_length": 33}
{"curie": "MONDO:0024483", "names": ["urothelium hyperplasia", "urothelial hyperplasia", "Urothelial Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urothelial hyperplasia", "shortest_name_length": 22}
{"curie": "UMLS:C3495700", "names": ["Atypical fracture"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypical fracture", "shortest_name_length": 17}
{"curie": "MONDO:0013287", "names": ["AGM2", "lambda 5 deficiency", "agammaglobulinemia 2", "IGLL1 autosomal agammaglobulinemia", "agammaglobulinemia 2, autosomal recessive", "AGAMMAGLOBULINEMIA 2, AUTOSOMAL RECESSIVE", "autosomal agammaglobulinemia caused by mutation in IGLL1", "AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO IGLL1 DEFECT", "agammaglobulinemia, autosomal recessive, due to IGLL1 defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "agammaglobulinemia 2, autosomal recessive", "shortest_name_length": 4}
{"curie": "MONDO:0023757", "names": ["Roth", "MERALGIA PARESTHETICA", "Meralgia paresthetica", "meralgia paresthetica", "Meralgia Paresthetica", "MERALGIA PARAESTHETICA", "Meralgia paraesthetica", "PARESTHESIA, BERNHARDT", "bernhardt-rot syndrome", "Bernhardt-Rot syndrome", "meralgia paraesthetica", "Bernhardt-Roth Syndrome", "Bernhardt-Roth syndrome", "Bernhardt Roth Syndrome", "Bernhardt's paresthesia", "BERNHARDT-ROTH SYNDROME", "bernhardt-roth syndrome", "bernhardt's paresthesia", "Meralgia para-aesthetica", "meralgia para aesthetica", "Bernhardt's paraesthesia", "Meralgia paresthetica (disorder)", "[OBSOLETE] Meralgia paresthetica", "meralgia paresthetica (diagnosis)", "meralgia paraesthetica familial (type)", "n.cutaneus femoris lateralis; syndrome", "n.cutaneus femoris lateralis; disorder", "lateral femoral cutaneous nerve entrapment", "Lateral Femoral Cutaneous Nerve Entrapment", "Meralgia paresthetica, unspecified lower limb", "entrapment of lateral cutaneous nerve of thigh", "Entrapment of lateral cutaneous nerve of thigh", "Lateral cutaneous femoral nerve of thigh syndrome", "lateral cutaneous femoral nerve of thigh syndrome", "compression of lateral cutaneous femoral nerve of thigh", "Compression of lateral cutaneous femoral nerve of thigh", "Lateral cutaneous femoral nerve of thigh compression or syndrome", "entrapment; neuropathic, nerve, lateral cutaneous nerve of thigh"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "meralgia paresthetica", "shortest_name_length": 4}
{"curie": "MONDO:0006414", "names": ["skin sarcoma", "Skin Sarcoma", "sarcomas skin", "Sarcoma of Skin", "sarcoma of skin", "Sarcoma of skin", "cutaneous sarcoma", "Cutaneous sarcoma", "Cutaneous Sarcoma", "Sarcoma of the Skin", "sarcoma of the skin", "zone of skin sarcoma", "sarcoma of zone of skin", "sarcoma of skin (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin sarcoma", "shortest_name_length": 12}
{"curie": "MONDO:0800157", "names": ["inborn disorder of lysine, hydroxylysine, and tryptophan metabolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of lysine, hydroxylysine, and tryptophan metabolism", "shortest_name_length": 67}
{"curie": "UMLS:C0853942", "names": ["tongue blister", "blister tongue", "blisters tongue", "blistered tongue", "tongue blistering", "Tongue blistering", "blistering tongue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tongue blistering", "shortest_name_length": 14}
{"curie": "UMLS:C0856240", "names": ["injury home", "home injury", "home injuries", "Domestic injury", "Domestic Injury", "injury in the home", "Injury in the home"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Domestic injury", "shortest_name_length": 11}
{"curie": "UMLS:C4683519", "names": ["Adrenal Cortex Carcinoma by AJCC v7 Stage", "Adrenal Cortical Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adrenal Cortical Carcinoma by AJCC v7 Stage", "shortest_name_length": 41}
{"curie": "MONDO:0003646", "names": ["rectal NET", "rectum NET", "NET of the rectum", "rectum neuroendocrine tumor", "rectum neuroendocrine neoplasm", "rectal neuroendocrine neoplasm", "neuroendocrine tumor of rectum", "Rectal Neuroendocrine Neoplasm", "neuroendocrine neoplasm of rectum", "Neuroendocrine Neoplasm of Rectum", "Neuroendocrine neoplasm of rectum", "neuroendocrine neoplasm of the rectum", "Neuroendocrine Neoplasm of the Rectum", "Neuroendocrine neoplasm of rectum (disorder)", "rectum neuroendocrine tumor, well differentiated, low or intermediate grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rectum neuroendocrine neoplasm", "shortest_name_length": 10}
{"curie": "MONDO:0001538", "names": ["Ischemia retinal", "retinal ischemia", "Retinal ischemia", "ischemia; retina", "ISCHEMIA RETINAL", "Retinal ischaemia", "Ischaemia retinal", "retina ischemic disease", "ischemic disease of retina", "Retinal ischemia (disorder)", "retinal ischemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal ischemia", "shortest_name_length": 16}
{"curie": "UMLS:C0334096", "names": ["Intimal Hyperplasia", "Intimal hyperplasia", "Intimal proliferation", "Intimal Proliferation", "PROLIFERATION, INTIMA", "Proliferation, intimal", "Intimal proliferation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intimal proliferation", "shortest_name_length": 19}
{"curie": "UMLS:C5444889", "names": ["IDUS", "Idiopathic Dysplasia of Uncertain Significance", "Idiopathic Dysplasia of Undetermined/Uncertain Significance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Idiopathic Dysplasia of Uncertain Significance", "shortest_name_length": 4}
{"curie": "MONDO:0011845", "names": ["MGR3", "migraine with or without aura, susceptibility to, 3", "MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 3", "migraine with or without aura, susceptibility to, type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "migraine with or without aura, susceptibility to, 3", "shortest_name_length": 4}
{"curie": "MONDO:0012899", "names": ["AGA3", "alopecia, androgenetic, 3", "ALOPECIA, ANDROGENETIC, 3", "Alopecia, Androgenetic, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alopecia, androgenetic, 3", "shortest_name_length": 4}
{"curie": "UMLS:C5555709", "names": ["Recurrent Malignant Retroperitoneal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Malignant Retroperitoneal Neoplasm", "shortest_name_length": 44}
{"curie": "UMLS:C1335364", "names": ["Parotid Gland MALT Lymphoma", "Parotid Gland Mucosa-Associated Lymphoid Tissue Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parotid Gland Mucosa-Associated Lymphoid Tissue Lymphoma", "shortest_name_length": 27}
{"curie": "MONDO:0016864", "names": ["Okihiro syndrome due to a point mutation", "Duane-radial ray syndrome due to a point mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Okihiro syndrome due to a point mutation", "shortest_name_length": 40}
{"curie": "MONDO:0100497", "names": ["titinopathy with congenital contractures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "titinopathy with congenital contractures", "shortest_name_length": 40}
{"curie": "MONDO:0013095", "names": ["GLM6", "glioma susceptibility 6", "GLIOMA SUSCEPTIBILITY 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glioma susceptibility 6", "shortest_name_length": 4}
{"curie": "UMLS:C4526914", "names": ["Lung Non-Mucinous Adenocarcinoma In Situ", "Non-mucinous adenocarcinoma in situ of lung", "Non-mucinous adenocarcinoma in situ of lung (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-mucinous adenocarcinoma in situ of lung", "shortest_name_length": 40}
{"curie": "MONDO:0005137", "names": ["Underfed", "Deficiency", "malnutrition", "Deficit, NOS", "MALNUTRITION", "Malnutrition", "MALNOURISHED", "malnourished", "Malnourished", "nutrition poor", "UNDERNOURISHED", "Malnourishment", "POOR NUTRITION", "Undernutrition", "undernutrition", "undernourished", "poor nutrition", "Undernourished", "Malnourishments", "deficiency; diet", "Deficiency state", "Malnutrition NOS", "diet; deficiency", "nutrition disease", "disease nutrition", "nutrition diseases", "disorder nutrition", "Nutrition Disorder", "diseases nutrition", "nutrition disorder", "DIETARY DEFICIENCY", "dietary deficiency", "Dietary deficiency", "Nutrition Disorders", "Nutrition disorders", "Problem;nutritional", "disorders nutrition", "nutrition disorders", "disease nutritional", "nutritional problem", "nutritional disease", "Undernutrition, NOS", "Acquired deficiency", "Nutritional disease", "diseases nutritional", "Nutritional disorder", "nutritional problems", "nutritional disorder", "Nutritional Disorder", "Disorder;nutritional", "Nutritional problems", "Diseases of Nutrition", "Nutritional Disorders", "nutritional; disorder", "Malnutrition syndrome", "nutritional disorders", "Disorder of nutrition", "NUTRITIONAL DISORDERS", "disorder; nutritional", "Nutritional deficiency", "Deficiency;nutritional", "deficiency nutritional", "insufficiency; dietary", "nutritional deficiency", "Malnutrition (E40-E46)", "Nutritional Deficiency", "deficiency; nutritional", "Undernutrition syndrome", "nutritional; deficiency", "deficiencies nutritional", "nutritional deficiencies", "Nutritional deficiencies", "Undernourished (finding)", "Nutritional Deficiencies", "NUTRITIONAL DEFICIENCIES", "Nutritional disease, NOS", "malnutrition (diagnosis)", "Nutritional disorder, NOS", "Undernutrition (disorder)", "nourishment; insufficiency", "insufficiency; nourishment", "Nutritional deficiency, NOS", "Nutritional deficiency state", "Undernutrition syndrome, NOS", "Nutritional deficiency finding", "Nutritional disorder (disorder)", "Nutritional deficiency disorder", "deficiency disorders nutritional", "nutritional disorder (diagnosis)", "Nutritional deficiency (finding)", "undernourished (physical finding)", "Unspecified nutritional deficiency", "deficiencies disorders nutritional", "Nutritional deficiency, unspecified", "nutritional deficiencies (diagnosis)", "NUTRITIONAL DISORDERS: GENERAL TERMS", "Nutritional deficiency disorder, NOS", "Nutritional deficiency disorder (disorder)", "disease (or disorder); nutritional deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nutritional disorder", "shortest_name_length": 8}
{"curie": "MONDO:0001113", "names": ["fiedler myocarditis", "Fiedler; myocarditis", "Isolated myocarditis", "myocarditis; Fiedler", "myocarditis isolated", "Myocarditis, isolated", "Fiedler's myocarditis", "isolated; myocarditis", "myocarditis; isolated", "fiedler's myocarditis", "idiopathic myocarditis", "Idiopathic myocarditis", "Myocarditis, Fiedler's", "myocarditis; idiopathic", "idiopathic; myocarditis", "Isolated (Fiedler's) myocarditis", "myocarditis isolated (diagnosis)", "isolated (Fiedler's) myocarditis", "Idiopathic myocarditis (disorder)", "idiopathic myocarditis (diagnosis)", "Isolated (Fiedler's) myocarditis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fiedler's myocarditis", "shortest_name_length": 19}
{"curie": "UMLS:C0521761", "names": ["Non-fatigable positional nystagmus", "Non-Fatigable Positional Nystagmus", "Non Fatigable Positional Nystagmus", "Positional Nystagmus, Non-Fatigable", "Nystagmus, Non-Fatigable Positional", "Non-fatigable positional nystagmus (disorder)", "Non-fatigable positional nystagmus (diagnosis)", "nystagmus non-fatigable positional non-fatigable"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Fatigable Positional Nystagmus", "shortest_name_length": 34}
{"curie": "UMLS:C4721430", "names": ["stage IV ovarian germ cell tumor", "Stage IV Ovarian Germ Cell Tumor", "Stage IV Ovarian Germ Cell Tumor AJCC v7", "Stage IV Ovarian Germ Cell Tumor AJCC v6", "Stage IV Malignant Ovarian Germ Cell Tumor", "Stage IV Malignant Germ Cell Tumor of Ovary", "Stage IV Malignant Ovarian Germ Cell Neoplasm", "Stage IV Malignant Germ Cell Neoplasm of Ovary", "Stage IV Ovarian Germ Cell Tumor AJCC v6 and v7", "Stage IV Malignant Germ Cell Tumor of the Ovary", "Stage IV Malignant Germ Cell Neoplasm of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Ovarian Germ Cell Tumor AJCC v6 and v7", "shortest_name_length": 32}
{"curie": "MONDO:0013294", "names": ["ATOD8", "atopic dermatitis 8", "dermatitis, atopic, 8", "DERMATITIS, ATOPIC, 8", "atopic dermatitis type 8", "dermatitis, atopic, severity of", "DERMATITIS, ATOPIC, SEVERITY OF", "dermatitis, atopic, susceptibility to, 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermatitis, atopic, 8", "shortest_name_length": 5}
{"curie": "UMLS:C5419803", "names": ["Rectal Neuroendocrine Tumor G3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rectal Neuroendocrine Tumor G3", "shortest_name_length": 30}
{"curie": "UMLS:C4054736", "names": ["Incident Nephrotic Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Incident Nephrotic Syndrome", "shortest_name_length": 27}
{"curie": "MONDO:0000410", "names": ["Funisitis", "funisitis", "Funisitides", "Funisitis (disorder)", "inflammation of umbilical cord", "Inflammation of umbilical cord", "inflammation of umbilical cord (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "funisitis", "shortest_name_length": 9}
{"curie": "MONDO:0009373", "names": ["HYDROXYLYSINURIA", "hydroxylysinuria", "Hydroxylysinuria", "Hydroxylysine high in urine", "seizures-intellectual disability due to hydroxylysinuria syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "seizures-intellectual disability due to hydroxylysinuria syndrome", "shortest_name_length": 16}
{"curie": "UMLS:C0237021", "names": ["ovarian complex cyst", "complex cyst ovarian", "complex ovarian cyst", "Complex Ovarian Cyst", "ovarian cyst complex", "Complex ovarian cyst", "Complex Cyst of Ovary", "complex cysts ovarian", "Complex cyst of ovary", "Complex Cyst of the Ovary", "Complex Cystic Ovarian Tumor", "Complex Cystic Tumor of Ovary", "Complex Cystic Ovarian Neoplasm", "Complex ovarian cyst (disorder)", "Complex Cystic Neoplasm of Ovary", "Complex ovarian cyst (diagnosis)", "Complex Cystic Tumor of the Ovary", "Complex Cystic Neoplasm of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Complex ovarian cyst", "shortest_name_length": 20}
{"curie": "MONDO:0012998", "names": ["FACIOCARDIOMELIC SYNDROME", "Faciocardiomelic Syndrome", "faciocardiomelic syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "faciocardiomelic syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0022901", "names": ["Crohn's esophagitis", "crohn's esophagitis", "Crohn's oesophagitis", "crohn's disease esophagus", "Crohn disease of esophagus", "Crohn disease of oesophagus", "Crohn's disease of esophagus", "Crohn's disease of oesophagus", "Crohn disease of the esophagus", "Crohn's disease of the esophagus", "Crohn's disease of esophagus (disorder)", "Crohn's disease of esophagus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Crohn disease of the esophagus", "shortest_name_length": 19}
{"curie": "MONDO:0002655", "names": ["cutaneous Paget disease", "Paget's disease of skin", "cutaneous Paget's disease", "zone of skin Paget disease", "extramammary Paget's disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous Paget disease", "shortest_name_length": 23}
{"curie": "MONDO:0005687", "names": ["Calicivirus infection", "infection, Calicivirus", "Calicivirus infections", "Caliciviridae Infection", "infections, Calicivirus", "Caliciviridae infection", "Caliciviridae Infections", "infection, Caliciviridae", "Infection, Caliciviridae", "Infections, Caliciviridae", "infections, Caliciviridae", "Caliciviridae infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Caliciviridae infectious disease", "shortest_name_length": 21}
{"curie": "UMLS:C1333786", "names": ["Gastric Precancerous Condition", "Gastric Premalignant Condition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Precancerous Condition", "shortest_name_length": 30}
{"curie": "UMLS:C4743562", "names": ["Recurrent Thyroid Gland Anaplastic Carcinoma", "Recurrent Thyroid Gland Undifferentiated (Anaplastic) Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Thyroid Gland Anaplastic Carcinoma", "shortest_name_length": 44}
{"curie": "UMLS:C1332483", "names": ["Benign Pediatric CNS Tumor", "Benign Childhood CNS Tumor", "Benign Childhood CNS Neoplasm", "Benign Childhood Tumor of CNS", "Benign Pediatric Tumor of CNS", "Benign Pediatric CNS Neoplasm", "Benign Pediatric Neoplasm of CNS", "Benign Childhood Neoplasm of CNS", "Benign Childhood Tumor of the CNS", "Benign Pediatric Tumor of the CNS", "Benign Pediatric Neoplasm of the CNS", "Benign Childhood Neoplasm of the CNS", "Benign Central Nervous System Neoplasm", "Benign Childhood Central Nervous System Tumor", "Benign Pediatric Central Nervous System Tumor", "Benign Pediatric Central Nervous System Neoplasm", "Benign Childhood Central Nervous System Neoplasm", "Benign Pediatric Tumor of Central Nervous System", "Benign Childhood Tumor of Central Nervous System", "Childhood Benign Central Nervous System Neoplasms", "Benign Childhood Neoplasm of Central Nervous System", "Benign Pediatric Neoplasm of Central Nervous System", "Benign Pediatric Tumor of the Central Nervous System", "Benign Childhood Tumor of the Central Nervous System", "Benign Childhood Neoplasm of the Central Nervous System", "Benign Pediatric Neoplasm of the Central Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Childhood Central Nervous System Neoplasm", "shortest_name_length": 26}
{"curie": "UMLS:C1332471", "names": ["Benign Anal Myoblastoma", "Benign Myoblastoma of Anus", "Benign Myoblastoma of the Anus", "Benign Anal Granular Cell Tumor", "Benign Anal Granular Cell Neoplasm", "Benign Granular Cell Tumor of Anus", "Benign Granular Cell Neoplasm of Anus", "Benign Granular Cell Tumor of the Anus", "Benign Granular Cell Neoplasm of the Anus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Anal Granular Cell Tumor", "shortest_name_length": 23}
{"curie": "MONDO:0017759", "names": ["Disorder of catecholamine synthesis", "disorder of catecholamine synthesis", "Disorder of catecholamine synthesis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of catecholamine synthesis", "shortest_name_length": 35}
{"curie": "MONDO:0015179", "names": ["intestinal disease due to vitamin absorption anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intestinal disease due to vitamin absorption anomaly", "shortest_name_length": 52}
{"curie": "MONDO:0011253", "names": ["craniomicromelic syndrome", "Craniomicromelic Syndrome", "CRANIOMICROMELIC SYNDROME", "Craniomicromelic syndrome", "Craniomicromelic syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniomicromelic syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0005701", "names": ["Chlamydia", "chlamydia", "chlamydial disease", "Chlamydial Infection", "Chlamydial infection", "chlamydia trachomatis infectious disease", "Chlamydia trachomatis infectious disease", "Chlamydia trachomatis disease or disorder", "Chlamydia trachomatis caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chlamydia trachomatis infectious disease", "shortest_name_length": 9}
{"curie": "MONDO:0001519", "names": ["Entropion", "entropion", "ENTROPION", "Entropions", "Entropion NOS", "Entropion;eye", "Entropion, NOS", "eyelids turning", "Eyelid inverted", "Inverted eyelid", "Eyelid turned in", "eyelids inverted", "Eyelid folded in", "Folded in eyelid", "Entropion of eyelid", "Eyelashes turned in", "entropion (disease)", "Eyelid turned inward", "entropion (diagnosis)", "Entropion, unspecified", "entropion was observed", "entropion (physical finding)", "Entropion of eyelid (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "entropion", "shortest_name_length": 9}
{"curie": "MONDO:0020652", "names": ["immature teratoma of vulva"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immature teratoma of vulva", "shortest_name_length": 26}
{"curie": "MONDO:0016077", "names": ["Aortopulmonary fistula", "aortopulmonary fistula", "Aorta-pulmonary artery fistula", "Aorto-pulmonary artery fistula", "aorto-pulmonary artery fistula", "aorta-pulmonary artery fistula", "congenital aortopulmonary window", "congenital aortopulmonary septal defect", "congenital aortopulmonary artery fistula"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital aortopulmonary window", "shortest_name_length": 22}
{"curie": "UMLS:C0555970", "names": ["nose infection", "infection nose", "infection nasal", "Infection;nasal", "NASAL INFECTION", "infections nose", "nasal infection", "Nasal infection", "infections nasal", "Nose infection NOS", "Nasal infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasal infection", "shortest_name_length": 14}
{"curie": "MONDO:0013031", "names": ["PVNH5", "periventricular nodular heterotopia 5", "PERIVENTRICULAR NODULAR HETEROTOPIA 5", "Periventricular Nodular Heterotopia 5", "CHROMOSOME 5q14.3 DELETION SYNDROME, DISTAL", "chromosome 5Q14.3 deletion syndrome, distal", "Heterotopia, Periventricular, Associated With Chromosome 5q Deletion", "HETEROTOPIA, PERIVENTRICULAR, ASSOCIATED WITH CHROMOSOME 5q DELETION", "heterotopia, periventricular, associated with chromosome 5Q deletion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 5Q14.3 deletion syndrome, distal", "shortest_name_length": 5}
{"curie": "MONDO:0030360", "names": ["PFIC6", "CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 6", "cholestasis, progressive familial intrahepatic, 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholestasis, progressive familial intrahepatic, 6", "shortest_name_length": 5}
{"curie": "UMLS:C3897199", "names": ["Venous Stroke", "Cerebral Venous Stroke", "Cerebral Thrombotic Stroke"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Venous Stroke", "shortest_name_length": 13}
{"curie": "MONDO:0008741", "names": ["PAGOD syndrome", "PAGOD SYNDROME", "Kennerknecht sorgo Oberhoffer syndrome", "Kennerknecht Sorgo Oberhoffer syndrome", "Agonadism dextrocardia diaphragmatic hernia", "Agonadism with multiple internal malformations", "AGONADISM WITH MULTIPLE INTERNAL MALFORMATIONS", "agonadism with multiple internal malformations", "Pulmonary hypoplasia-agonadism-dextrocardia-diaphragmatic hernia syndrome", "pulmonary hypoplasia-agonadism-dextrocardia-diaphragmatic hernia syndrome", "Pulmonary hypoplasia, agonadism, dextrocardia, diaphragmatic hernia syndrome", "Pulmonary hypoplasia, agonadism, dextrocardia, diaphragmatic hernia syndrome (disorder)", "PAGOD (pulmonary hypoplasia, hypoplasia pulmonary artery, agonadism, omphalocele, dextrocardia) syndrome", "pulmonary hypoplasia, hypoplasia of the pulmonary artery, agonadism, omphalocele-diaphragmatic defect, and dextrocardia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PAGOD syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0014444", "names": ["BBS16", "BARDET-BIEDL SYNDROME 16", "Bardet-Biedl syndrome 16", "Bardet-Biedl syndrome type 16", "SDCCAG8 Bardet-Biedl syndrome", "Bardet-Biedl syndrome caused by mutation in SDCCAG8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bardet-Biedl syndrome 16", "shortest_name_length": 5}
{"curie": "UMLS:C4743637", "names": ["Resectable Renal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Renal Cell Carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0044646", "names": ["PEBAT", "early onset progressive encephalopathy with brain atrophy and thin corpus callosum", "early-onset progressive encephalopathy with brain atrophy and thin corpus callosum", "encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum", "ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM", "encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum; PEBAT", "early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0003084", "names": ["Uremic Neuropathy", "uremic neuropathy", "Uremic neuropathy", "NEUROPATHY UREMIC", "Neuropathy, uremic", "Uraemic neuropathy", "Uremic neuropathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uremic neuropathy", "shortest_name_length": 17}
{"curie": "UMLS:C1266118", "names": ["Cellular fibroma", "Cellular Fibroma", "Cellular fibroma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cellular fibroma", "shortest_name_length": 16}
{"curie": "MONDO:0100510", "names": ["SEMD", "Spondyloepimetaphyseal disorder", "spondyloepimetaphyseal dysplasia", "Spondyloepimetaphyseal dysplasia", "spondylo-epi-(meta)-physeal dysplasia", "Spondyloepimetaphyseal disorder (disorder)", "spondyloepimetaphyseal dysplasia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepimetaphyseal dysplasia", "shortest_name_length": 4}
{"curie": "UMLS:C0877095", "names": ["Application site bruise", "Application site purpura", "Application site hematoma", "Application site bruising", "Application site haematoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Application site hematoma", "shortest_name_length": 23}
{"curie": "MONDO:0014611", "names": ["MMDS4", "multiple mitochondrial dysfunctions syndrome 4", "MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 4", "Multiple mitochondrial dysfunctions syndrome type 4", "multiple mitochondrial dysfunctions syndrome type 4", "ISCA2 fatal multiple mitochondrial dysfunctions syndrome", "MMDS4 - multiple mitochondrial dysfunctions syndrome type 4", "Multiple mitochondrial dysfunctions syndrome type 4 (disorder)", "fatal multiple mitochondrial dysfunctions syndrome caused by mutation in ISCA2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple mitochondrial dysfunctions syndrome 4", "shortest_name_length": 5}
{"curie": "MONDO:0004514", "names": ["Chronic Rhinitis", "chronic rhinitis", "rhinitis chronic", "RHINITIS CHRONIC", "Rhinitis;chronic", "Chronic rhinitis", "Rhinitis, chronic", "rhinitis; chronic", "rhinitis, chronic", "chronic; rhinitis", "rhinitis - chronic", "Rhinitis - chronic", "Rhinitis (chronic) NOS", "Chronic rhinitis (disorder)", "chronic rhinitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic rhinitis", "shortest_name_length": 16}
{"curie": "MONDO:0005522", "names": ["small bowel cancer", "Small Bowel Cancer", "cancer of small bowel", "Small Bowel Carcinoma", "Cancer of Small Bowel", "small bowel carcinoma", "Small Intestine Cancer", "small intestine cancer", "small intestinal cancer", "Small Intestinal Cancer", "Carcinoma of Small Bowel", "carcinoma of small bowel", "Carcinoma of small bowel", "carcinoma small intestine", "Carcinoma;intestine;small", "carcinoma intestine small", "small intestine carcinoma", "Cancer of the Small Bowel", "Small intestine carcinoma", "cancer of the small bowel", "Small Intestinal Carcinoma", "small intestinal carcinoma", "small intestine cancer, NOS", "INTESTINE, SMALL, CARCINOMA", "Small intestine cancer, NOS", "Carcinoma of Small Intestine", "Carcinoma of small intestine", "carcinoma of small intestine", "Carcinoma of the Small Bowel", "carcinoma of the small bowel", "Small intestine carcinoma NOS", "carcinoma of the small intestine", "Carcinoma of the Small Intestine", "INTESTINE, SMALL, CANCER, CARCINOMA", "carcinoma of small intestine (diagnosis)", "Malignant epithelial neoplasm of small intestine", "Malignant epithelial neoplasm of small intestine (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small intestine carcinoma", "shortest_name_length": 18}
{"curie": "MONDO:0018659", "names": ["partial trisomy of chromosome 19p", "partial duplication of chromosome 19p", "partial trisomy of the short arm of chromosome 19", "partial duplication of the short arm of chromosome 19", "partial duplication of the short arm of chromosome type 19"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of the short arm of chromosome 19", "shortest_name_length": 33}
{"curie": "UMLS:C0280367", "names": ["Relapsed Mouth Adenoid Cystic Carcinoma", "Recurrent Mouth Adenoid Cystic Carcinoma", "Relapsed Adenoid Cystic Carcinoma of Mouth", "Recurrent Oral Cavity Adenoid Cystic Cancer", "Recurrent Adenoid Cystic Carcinoma of Mouth", "Relapsed Oral Cavity Adenoid Cystic Carcinoma", "Relapsed Adenoid Cystic Carcinoma of the Mouth", "Recurrent Oral Cavity Adenoid Cystic Carcinoma", "Recurrent Adenoid Cystic Carcinoma of the Mouth", "oral cavity adenoid cystic carcinoma, recurrent", "Relapsed Adenoid Cystic Carcinoma of Oral Cavity", "Recurrent Adenoid Cystic Carcinoma of Oral Cavity", "Relapsed Adenoid Cystic Carcinoma of the Oral Cavity", "recurrent adenoid cystic carcinoma of the oral cavity", "Adenoid cystic carcinoma of the oral cavity recurrent", "Recurrent Adenoid Cystic Carcinoma of the Oral Cavity", "adenoid cystic carcinoma of the oral cavity, recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenoid cystic carcinoma of the oral cavity recurrent", "shortest_name_length": 39}
{"curie": "MONDO:0002331", "names": ["nephroses", "Nephrosis", "Nephroses", "nephrosis", "NEPHROSIS", "Nephrosis NOS", "Nephrosis, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrosis", "shortest_name_length": 9}
{"curie": "UMLS:C1997862", "names": ["chronic post-traumatic stress disorder with associated nightmares", "Nightmares associated with chronic post-traumatic stress disorder", "Nightmares associated with chronic post-traumatic stress disorder (disorder)", "chronic post-traumatic stress disorder with associated nightmares (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nightmares associated with chronic post-traumatic stress disorder", "shortest_name_length": 65}
{"curie": "MONDO:0021439", "names": ["benign pituitary tumor", "Pituitary tumor benign", "Benign Pituitary Tumor", "Pituitary Tumor, Benign", "pituitary tumor, benign", "Pituitary tumour benign", "benign pituitary tumors", "Benign Tumor of Pituitary", "benign pituitary neoplasm", "benign tumor of pituitary", "PITUITARY NEOPLASM BENIGN", "Pituitary neoplasm benign", "Benign Pituitary Neoplasm", "Pituitary tumor benign NOS", "Pituitary Neoplasms, Benign", "pituitary neoplasms, benign", "Pituitary tumour benign NOS", "Benign Pituitary Gland Tumor", "benign neoplasm of pituitary", "Benign Neoplasm of Pituitary", "benign gland pituitary tumor", "benign pituitary gland tumor", "benign tumor of the pituitary", "Benign Tumor of the Pituitary", "benign pituitary gland neoplasm", "pituitary gland benign neoplasm", "Benign tumor of pituitary gland", "Benign Tumor of Pituitary Gland", "benign tumor of pituitary gland", "Benign Pituitary Gland Neoplasm", "Benign Neoplasm of the Pituitary", "Benign tumour of pituitary gland", "benign neoplasm of the pituitary", "Benign neoplasm of pituitary gland", "benign neoplasm of pituitary gland", "Benign Neoplasm of Pituitary Gland", "Benign Tumor of the Pituitary Gland", "benign tumor of the pituitary gland", "benign neoplasm of the pituitary gland", "Benign Neoplasm of the Pituitary Gland", "Benign neoplasm of pituitary gland (disorder)", "benign neoplasm of pituitary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of pituitary gland", "shortest_name_length": 22}
{"curie": "MONDO:0006469", "names": ["tibia adamantinoma", "Tibial adamantinoma", "adamantinoma; tibia", "tibia; adamantinoma", "Tibial Adamantinoma", "tibial adamantinoma", "tibia; ameloblastoma", "ameloblastoma; tibia", "adamantinoma of tibia", "tibia long bone adamantinoma", "Tibial adamantinoma morphology", "Tibial adamantinoma (disorder)", "tibial adamantinoma morphology", "Tibial adamantinoma (diagnosis)", "Tibial adamantinoma (morphologic abnormality)", "bone neoplasm, malignant - long bones of lower limb tibial adamantinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tibial adamantinoma", "shortest_name_length": 18}
{"curie": "MONDO:0008257", "names": ["PLATELET RESPONSIVENESS TO ADRENALINE, DEPRESSED", "platelet responsiveness to adrenaline, depressed"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "platelet responsiveness to adrenaline, depressed", "shortest_name_length": 48}
{"curie": "UMLS:C1699210", "names": ["Intraoperative Neurological Injury", "intraoperative neurological injury", "Intraoperative neurological injury", "intraoperative neurological injury (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraoperative Neurological Injury", "shortest_name_length": 34}
{"curie": "UMLS:C1960034", "names": ["Sexual dysfunction due to substance", "Substance-induced sexual dysfunction", "Substance-Induced Sexual Dysfunction", "Sexual dysfunction caused by substance", "Sexual dysfunction caused by substance (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sexual dysfunction due to substance", "shortest_name_length": 35}
{"curie": "UMLS:C4727070", "names": ["Advanced Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Carcinoma", "shortest_name_length": 18}
{"curie": "UMLS:C1512249", "names": ["Grade 1 Endometrial Endometrioid Carcinoma", "Grade 1 Endometrial Endometrioid Adenocarcinoma", "FIGO Grade 1 Endometrial Endometrioid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Grade 1 Endometrial Endometrioid Adenocarcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0021101", "names": ["Appendix L-Cell NET", "appendix L-cell NET", "malignant appendiceal glucagonoma", "Appendix L-Cell Glucagon-Like Peptide-Producing NET", "appendix L-cell glucagon-like peptide-producing NET", "appendiceal L-cell glucagon-like peptide-producing NET", "Appendiceal L-Cell Glucagon-Like Peptide-Producing NET", "appendiceal L-cell glucagon-like peptide producing tumor", "appendiceal L-cell glucagon-like peptide producing tumour", "malignant appendiceal L-cell glucagon-like peptide producing tumor", "malignant appendiceal L-cell glucagon-like peptide producing tumour", "appendix L-cell glucagon-like peptide-producing neuroendocrine tumor", "Appendix L-Cell Glucagon-Like Peptide-Producing Neuroendocrine Tumor", "appendiceal L-cell glucagon-like peptide-producing neuroendocrine tumor", "Appendiceal L-Cell Glucagon-Like Peptide-Producing Neuroendocrine Tumor", "vermiform appendix L-cell glucagon-like peptide-producing neuroendocrine tumor", "L-cell glucagon-like peptide-producing neuroendocrine tumor of vermiform appendix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "appendix L-cell glucagon-like peptide-producing neuroendocrine tumor", "shortest_name_length": 19}
{"curie": "UMLS:C5237194", "names": ["Unresectable Neuroendocrine Tumor", "Unresectable Well Differentiated Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Neuroendocrine Tumor", "shortest_name_length": 33}
{"curie": "UMLS:C3897528", "names": ["Stage IIIB Rectal Cancer", "Stage IIIB Rectal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Rectal Cancer AJCC v7", "shortest_name_length": 24}
{"curie": "MONDO:0013569", "names": ["SRPS5", "SRTD7", "SRTD7/20", "short rib-polydactyly syndrom type V", "short rib-polydactyly syndrome type 5", "short rib-polydactyly syndrome type V", "short rib-polydactyly syndrome, type 5", "SHORT RIB-POLYDACTYLY SYNDROME, TYPE V", "short-rib thoracic dysplasia 7 with or without polydactyly", "SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY", "SHORT-RIB THORACIC DYSPLASIA 7/20 WITH POLYDACTYLY, DIGENIC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short-rib thoracic dysplasia 7 with or without polydactyly", "shortest_name_length": 5}
{"curie": "MONDO:0001851", "names": ["lacrimal atrophy primary", "primary lacrimal atrophy", "Primary lacrimal atrophy", "Primary lacrimal atrophy (disorder)", "primary lacrimal atrophy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary lacrimal atrophy", "shortest_name_length": 24}
{"curie": "MONDO:0010774", "names": ["Infantile Bilateral Striatal Necrosis, Mitochondrial", "STRIATONIGRAL DEGENERATION, INFANTILE, MITOCHONDRIAL", "infantile bilateral striatal Necrosis, mitochondrial", "Striatonigral Degeneration, Infantile, Mitochondrial", "INFANTILE BILATERAL STRIATAL NECROSIS, MITOCHONDRIAL", "striatonigral degeneration, infantile, mitochondrial", "Bilateral Striatal Necrosis, Infantile, Mitochondrial", "bilateral striatal Necrosis, infantile, mitochondrial", "BILATERAL STRIATAL NECROSIS, INFANTILE, MITOCHONDRIAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "striatonigral degeneration, infantile, mitochondrial", "shortest_name_length": 52}
{"curie": "UMLS:C1611195", "names": ["Congenital corneal dystrophy", "Congenital dystrophy of cornea", "Congenital dystrophy of cornea (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital corneal dystrophy", "shortest_name_length": 28}
{"curie": "MONDO:0019729", "names": ["LHCDD", "light and heavy chain deposition disease", "Light and Heavy Chain Deposition Disease", "Light and heavy chain deposition disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "light and heavy chain deposition disease", "shortest_name_length": 5}
{"curie": "MONDO:0012134", "names": ["EJM3", "juvenile myoclonic epilepsy 3", "epilepsy, juvenile myoclonic 3", "myoclonic epilepsy, juvenile, susceptibility to, 3", "MYOCLONIC EPILEPSY, JUVENILE, SUSCEPTIBILITY TO, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myoclonic epilepsy, juvenile, susceptibility to, 3", "shortest_name_length": 4}
{"curie": "UMLS:C0205641", "names": ["basal cell adenocarcinoma", "Basal cell adenocarcinoma", "Basal Cell Adenocarcinoma", "Basal Cell Adenocarcinomas", "Adenocarcinoma, Basal Cell", "Adenocarcinomas, Basal Cell", "[M] Basal cell adenocarcinoma", "basal cell adenocarcinoma (diagnosis)", "Basal cell adenocarcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma, Basal Cell", "shortest_name_length": 25}
{"curie": "MONDO:0016029", "names": ["Esthesioneuroblastoma", "Asthesioneuroblastoma", "esthesioneuroblastoma", "Esthesioneuroblastomas", "Aesthesioneuroblastoma", "esthesioneuroblastomas", "Aesthesioneuroblastomas", "olfactory neuroblastoma", "Olfactory Neuroblastoma", "Olfactory neuroblastoma", "Olfactory Neuroblastomas", "Neuroblastoma, Olfactory", "Esthesioneuroepithelioma", "esthesioneuroepithelioma", "Aesthesioneuroepithelioma", "Neuroblastomas, Olfactory", "Olfactory neuroepithelioma", "Olfactory Neuroepithelioma", "Olfactory Esthesioneuroblastoma", "Olfactory esthesioneuroblastoma", "esthesioneuroblastoma olfactory", "Esthesioneuroblastoma, Olfactory", "Olfactory Esthesioneuroblastomas", "Esthesioneuroblastomas, Olfactory", "Olfactory neuroblastoma (disorder)", "Nasal cavity esthesioneuroblastoma", "Olfactory neuroblastoma (diagnosis)", "Paranasal sinus esthesioneuroblastoma", "Accessory Sinus Esthesioneuroblastoma", "Paranasal Sinus Esthesioneuroblastoma", "Paranasal Sinus Olfactory Neuroblastoma", "Esthesioneuroblastoma of Accessory Sinus", "Esthesioneuroblastoma of Paranasal Sinus", "malignant neoplasm neuroblastoma olfactory", "Esthesioneuroblastoma of the Accessory Sinus", "Esthesioneuroblastoma of the Paranasal Sinus", "Esthesioneuroblastoma (morphologic abnormality)", "Paranasal Sinus-Nasal Cavity Esthesioneuroblastoma", "Esthesioneuroepithelioma (morphologic abnormality)", "Paranasal Sinus Nasal Cavity Esthesioneuroblastoma", "Esthesioneuroblastoma, Paranasal Sinus-Nasal Cavity", "Esthesioneuroblastoma, Paranasal Sinus Nasal Cavity", "paranasal sinus and nasal cavity esthesioneuroblastoma", "nasal cavity and paranasal sinus esthesioneuroblastoma", "esthesioneuroblastoma, paranasal sinus and nasal cavity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esthesioneuroblastoma", "shortest_name_length": 21}
{"curie": "MONDO:0032678", "names": ["DEE71", "EIEE71", "early infantile epileptic encephalopathy 71", "epileptic encephalopathy, early infantile, 71", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 71", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 71", "developmental and epileptic encephalopathy 71", "developmental and epileptic encephalopathy, 71", "GLUTAMINASE DEFICIENCY WITH NEONATAL EPILEPTIC ENCEPHALOPATHY", "Glutaminase Deficiency With Neonatal Epileptic Encephalopathy", "glutaminase deficiency with neonatal epileptic encephalopathy", "Neonatal epileptic encephalopathy due to glutaminase deficiency", "Neonatal epileptic encephalopathy due to deficiency of glutaminase", "Neonatal epileptic encephalopathy due to deficiency of glutaminase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 71", "shortest_name_length": 5}
{"curie": "UMLS:C2732622", "names": ["Exposure to varicella", "Exposure to varicella (event)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Exposure to varicella", "shortest_name_length": 21}
{"curie": "MONDO:0012096", "names": ["CMT2L", "Charcot-Marie-Tooth disease type 2L", "HSPB8 Charcot-Marie-Tooth disease type 2", "Charcot-Marie-Tooth disease axonal type 2L", "Charcot-Marie-Tooth disease, axonal, type 2L", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L", "Charcot-Marie-Tooth neuropathy axonal type 2L", "CHARCOT-MARIE-TOOTH NEUROPATHY, AXONAL, TYPE 2L", "Charcot-Marie-Tooth neuropathy, axonal, type 2L", "autosomal dominant Charcot-Marie-Tooth disease type 2L", "Autosomal dominant Charcot-Marie-Tooth disease type 2L", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L (disorder)", "autosomal dominant axonal Charcot-Marie-Tooth disease type 2L", "Charcot-Marie-Tooth disease type 2 caused by mutation in HSPB8", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2L", "Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2L", "Autosomal dominant Charcot-Marie-Tooth disease type 2L (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease axonal type 2L", "shortest_name_length": 5}
{"curie": "MONDO:0017543", "names": ["SD1b", "SD1, Lueken type", "syndactyly type 1b", "zygodactyly type 2", "Zygodactyly, Lueken type", "syndactyly type 1, Lueken type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "zygodactyly type 2", "shortest_name_length": 4}
{"curie": "MONDO:0008659", "names": ["TCI deficiency", "Tcn1 deficiency", "TCN1 DEFICIENCY", "R-binder deficiency", "Haptocorrin deficiency", "transcobalamin I deficiency", "Transcobalamin-1 deficiency", "TRANSCOBALAMIN I DEFICIENCY", "Transcobalamin I deficiency", "transcobalamin 1 deficiency", "Transcobalamin I Deficiency", "transcobalamin-1 deficiency", "COBALAMIN R BINDER PROTEIN DEFICIENCY", "cobalamin R Binder Protein deficiency", "Cobalamin R Binder Protein Deficiency", "Transcobalamin I deficiency (disorder)", "R Binder deficiency with lactoferrin deficiency", "R BINDER DEFICIENCY WITH LACTOFERRIN DEFICIENCY", "TRANSCOBALAMIN I DEFICIENCY WITH LACTOFERRIN DEFICIENCY", "Transcobalamin I Deficiency With Lactoferrin Deficiency", "transcobalamin 1 deficiency with lactoferrin deficiency", "COBALAMIN PSEUDODEFICIENCY DUE TO TRANSCOBALAMIN DEFICIENCY", "Cobalamin Pseudodeficiency due to Transcobalamin Deficiency", "cobalamin Pseudodeficiency due to transcobalamin deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transcobalamin I deficiency", "shortest_name_length": 14}
{"curie": "UMLS:C0279961", "names": ["Stage I Immunoblastic Lymphoma", "Stage I Adult Immunoblastic Lymphoma", "Ann Arbor Stage I Adult Immunoblastic Lymphoma", "stage I adult immunoblastic large cell lymphoma", "Stage I Adult Immunoblastic Large Cell Lymphoma", "Adult Immunoblastic Large Cell Lymphoma Stage I", "adult immunoblastic large cell lymphoma, stage I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Adult Immunoblastic Lymphoma", "shortest_name_length": 30}
{"curie": "MONDO:0010352", "names": ["MRX82", "XLID82", "X-linked mental retardation 82", "MENTAL RETARDATION, X-LINKED 82", "mental retardation, X-linked 82", "Mental Retardation, X-Linked 82", "intellectual disability, X-linked 82", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 82", "non-syndromic X-linked intellectual disability 82", "mental retardation, X-linked 82, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 82", "shortest_name_length": 5}
{"curie": "MONDO:0011087", "names": ["IBD2", "INFLAMMATORY BOWEL DISEASE 2", "Inflammatory Bowel Disease 2", "inflammatory bowel disease 2", "inflammatory bowel disease type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory bowel disease 2", "shortest_name_length": 4}
{"curie": "MONDO:0033534", "names": ["COXPD46", "combined oxidative phosphorylation defiency 46", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 46", "combined oxidative phosphorylation deficiency 46"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation deficiency 46", "shortest_name_length": 7}
{"curie": "UMLS:C5670578", "names": ["Recurrent Transformed Indolent B-Cell Non-Hodgkin Lymphoma to Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Transformed Indolent B-Cell Non-Hodgkin Lymphoma to Diffuse Large B-Cell Lymphoma", "shortest_name_length": 91}
{"curie": "MONDO:0005662", "names": ["BALANTIDIASIS", "Balantidiases", "Balantidiasis", "balantidiosis", "Balantidiosis", "balantidiasis", "B coli infection", "ciliary dysentery", "Ciliary dysentery", "B. coli Infection", "Infection, B. coli", "B. coli Infections", "Human balantidiasis", "Balantidium; colitis", "colitis; Balantidium", "Balantidial dysentery", "Balantidium Infection", "Balantidium; diarrhea", "diarrhea; Balantidium", "Balantidium Infections", "Balantidiasis (disorder)", "balantidiasis (diagnosis)", "Balantidium coli Infection", "Balantidium coli infection", "Balantidium coli Infections", "dysentery; Balantidium coli", "Balantidium coli; dysentery", "Disease due to Balantidiidae", "Balantidium coli; infestation", "infestation; Balantidium coli", "DISEASES DUE TO BALANTIDIIDAE", "Disease caused by Balantidiidae", "Disease caused by Balantidiidae (disorder)", "large-intestinal infection with Balantidium coli"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "balantidiasis", "shortest_name_length": 13}
{"curie": "UMLS:C3900198", "names": ["46,XY Disorder of Androgen Action"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XY Disorder of Androgen Action", "shortest_name_length": 33}
{"curie": "MONDO:0022357", "names": ["Acardia", "acardia", "Acardia (disorder)", "congenital acardia", "congenital absence of the heart"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital acardia", "shortest_name_length": 7}
{"curie": "MONDO:0018153", "names": ["ECD", "lipogranulomatosis", "Lipogranulomatosis", "Lipid granulomatosis", "Lipid Granulomatosis", "Granulomatosis, Lipid", "lipoid granulomatosis", "Erdheim-Chester disease", "erdheim-chester disease", "Erdheim Chester Disease", "Erdheim Chester disease", "chester disease erdheim", "Erdheim-Chester Disease", "erdheim chester disease", "Erdheim-Chester syndrome", "Polyostotic sclerosing histiocytosis", "polyostotic sclerosing histiocytosis", "Polyostotic Sclerosing Histiocytosis", "Polyostotic sclerosing histiocytosis (disorder)", "polyostotic sclerosing histiocytosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Erdheim-Chester disease", "shortest_name_length": 3}
{"curie": "MONDO:0032893", "names": ["PAMDDFS", "PACHYGYRIA, MICROCEPHALY, DEVELOPMENTAL DELAY, AND DYSMORPHIC FACIES, WITH OR WITHOUT SEIZURES", "pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures", "shortest_name_length": 7}
{"curie": "UMLS:C5555183", "names": ["Refractory Ovarian Mucinous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Ovarian Mucinous Adenocarcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0001074", "names": ["TIC DISORDER CHRONIC", "Chronic Tic Disorder", "Chronic tic disorder", "chronic tic disorder", "tic disorder, chronic", "chronic motor or vocal tic disorder", "Chronic motor or vocal tic disorder", "Chronic Motor or Vocal Tic Disorder", "Motor or Vocal Tic Disorder, Chronic", "Tic Disorder, Chronic Motor or Vocal", "chronic motor or vocal tic disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic tic disorder", "shortest_name_length": 20}
{"curie": "MONDO:0015844", "names": ["agenesis and aplasia of uterine body"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "agenesis and aplasia of uterine body", "shortest_name_length": 36}
{"curie": "MONDO:0004821", "names": ["Nasopharynx Disease", "nasopharynx disease", "Nasopharynx Diseases", "nasopharynx; disease", "Nasopharynx--Diseases", "Nasopharyngeal Disease", "nasopharyngeal disease", "disease of nasopharynx", "Nasopharyngeal Disorder", "Diseases of Nasopharynx", "disorder of nasopharynx", "Disease, Nasopharyngeal", "Nasopharyngeal disorder", "Nasopharyngeal Diseases", "Disorder of nasopharynx", "nasopharyngeal disorder", "Diseases, Nasopharyngeal", "disorder of postnasal space", "Disorder of postnasal space", "nasopharynx disease or disorder", "Disorder of PNS - postnasal space", "disease or disorder of nasopharynx", "disease (or disorder); nasopharynx", "Disorder of nasopharynx (disorder)", "disorder of nasopharynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasopharyngeal disorder", "shortest_name_length": 19}
{"curie": "UMLS:C0854726", "names": ["Stage I Subdiaphragmatic Mixed Cellularity Hodgkin Lymphoma", "Stage I Subdiaphragmatic Mixed Cellularity Hodgkin's Disease", "Hodgkin's disease mixed cellularity stage I subdiaphragmatic", "Stage I Subdiaphragmatic Mixed Cellularity Hodgkin's Lymphoma", "Stage I Mixed Cellularity Hodgkin's Disease below the Diaphragm", "Stage I Mixed Cellularity Hodgkin's Lymphoma below the Diaphragm", "Stage I Subdiaphragmatic Mixed Cellularity Classical Hodgkin Lymphoma", "Ann Arbor Stage I Subdiaphragmatic Mixed Cellularity Classic Hodgkin Lymphoma", "Ann Arbor Stage I Subdiaphragmatic Mixed Cellularity Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's disease mixed cellularity stage I subdiaphragmatic", "shortest_name_length": 59}
{"curie": "UMLS:C4744996", "names": ["Recurrent T-Cell/Histiocyte-Rich Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent T-Cell/Histiocyte-Rich Large B-Cell Lymphoma", "shortest_name_length": 54}
{"curie": "MONDO:0010078", "names": ["spondyloperipheral dysplasia", "Spondyloperipheral dysplasia", "SPONDYLOPERIPHERAL DYSPLASIA", "Spondyloperipheral Dysplasia", "Familial spondyloepiphyseal dysplasia", "Spondyloperipheral dysplasia short ulna", "Spondyloperipheral dysplasia (disorder)", "SPONDYLOPERIPHERAL DYSPLASIA WITH SHORT ULNA", "Spondyloperipheral Dysplasia With Short Ulna", "spondyloperipheral dysplasia with short ulna", "spondyloperipheral dysplasia-short ulna syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloperipheral dysplasia", "shortest_name_length": 28}
{"curie": "MONDO:0014117", "names": ["CMT4B3", "Charcot-Marie-Tooth disease type 4B3", "CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B3", "Charcot-Marie-Tooth disease, type 4B3", "SBF1 Charcot-Marie-Tooth disease type 4", "Charcot-Marie-Tooth disease type 4B3 (disorder)", "Charcot-Marie-Tooth disease type 4B3 (diagnosis)", "Charcot-Marie-Tooth disease with focally folded myelin", "Charcot-Marie-Tooth disease type 4 caused by mutation in SBF1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 4B3", "shortest_name_length": 6}
{"curie": "UMLS:C1336968", "names": ["Virus Related Lymphoma", "Virus-Related Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Virus-Related Lymphoma", "shortest_name_length": 22}
{"curie": "MONDO:0001318", "names": ["gastric dysfunction", "dysfunction; stomach", "Gastric function disorder", "Disorder stomach function", "stomach function disorder", "Disorder;stomach function", "Stomach function disorder", "functional gastric disease", "functional gastric disorder", "Functional gastric disorder", "disorder of stomach function", "Disorder of stomach function", "Disorder of gastric function", "disorder of gastric function", "Gastric function disorder NOS", "stomach; disorder (functional)", "Functional gastric disturbance", "functional gastric disturbance", "Functional disorder of stomach", "Disorder of function of stomach", "stomach; functional disturbance", "functional disorders of stomach", "disorder of function of stomach", "Disorders of function of stomach", "disorders of function of stomach", "Functional gastric disorder, NOS", "Functional gastric irritation, NOS", "Functional gastric disturbance, NOS", "Functional gastrointestinal disorder", "Disorder of function of stomach, NOS", "Functional Gastrointestinal Disorder", "Gastrointestinal Disorder, Functional", "Functional Gastrointestinal Disorders", "Gastrointestinal Disorders, Functional", "Functional gastrointestinal disturbance", "Functional disorder of stomach (disorder)", "Unspecified functional disorder of stomach", "Disorder of function of stomach (disorder)", "disease (or disorder); stomach (functional)", "disorders of function of stomach (diagnosis)", "Functional disorder of gastrointestinal tract", "Functional disorder of gastrointestinal tract (disorder)", "Dyspepsia and other specified disorders of function of stomach"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "functional gastric disease", "shortest_name_length": 19}
{"curie": "MONDO:0007240", "names": ["PCCD", "HBBD", "PFHBI", "Pfhbi", "PFHB1A", "Pfhb1a", "PfhbIa", "PFHBIA", "Lev disease", "Lev syndrome", "Lev's disease", "Familial PCCD", "Lev's syndrome", "Lenegre disease", "Lenegre syndrome", "Fascicular Block", "Fascicular block", "fascicular block", "fascicular blocks", "block; fascicular", "Fascicular Blocks", "Lenegre's disease", "fascicular; block", "Lenegre's Disease", "Block, Fascicular", "Blocks, Fascicular", "Lenegre's syndrome", "Lenegre-Lev disease", "BLOCK BUNDLE BRANCH", "Block;bundle branch", "Bundle branch block", "Bundle Branch Block", "Block bundle branch", "branch bundle block", "bundle-branch block", "bundle block branch", "Lev-Lenègre disease", "block bundle branch", "BUNDLE BRANCH BLOCK", "bundle branch block", "LENEGRE-LEV DISEASE", "Lenegre-Lev Disease", "Bundle-Branch Block", "block branch bundle", "Bundle-branch block", "Lenegre Lev disease", "blocks branch bundle", "Block, Bundle Branch", "Branch Block, Bundle", "Familial Lev disease", "Lenegre-Lev syndrome", "bundle-branch; block", "Block, Bundle-Branch", "Bundle-Branch Blocks", "block; bundle-branch", "Bundle Branch Blocks", "Blocks, Bundle Branch", "blocked branch bundle", "Branch Blocks, Bundle", "Blocks, Bundle-Branch", "Bundle branch block NOS", "Bundle-branch block NOS", "Familial Lenègre disease", "Bundle branch block, NOS", "Lev's disease (diagnosis)", "HEART BLOCK BUNDLE BRANCH", "Heart block bundle branch", "Lev's syndrome (disorder)", "BBB (bundle branch block)", "bundle branch heart block", "block branch bundle heart", "BBB - Bundle branch block", "Lev's syndrome (diagnosis)", "heart block, nonprogressive", "Heart Block, Nonprogressive", "HEART BLOCK, NONPROGRESSIVE", "fascicular block (diagnosis)", "Familial Lev-Lenègre disease", "Bundle branch block (disorder)", "bundle branch block fascicular", "bundle branch block (diagnosis)", "Hereditary bundle branch defect", "Familial progressive heart block", "Progressive familial heart block", "Bundle branch block, unspecified", "heart block, progressive, type IA", "Heart block progressive, familial", "Bundle Branch Block by ECG Finding", "Bundle Branch Block by EKG Finding", "Progressive cardiac conduction defect", "A-V block third degree Lev's syndrome", "CARDIAC CONDUCTION DEFECT, PROGRESSIVE", "SCN5A progressive familial heart block", "Hereditary bundle branch system defect", "HEREDITARY BUNDLE BRANCH SYSTEM DEFECT", "Cardiac conduction defect, progressive", "hereditary bundle branch system defect", "heart block progressive familial type 1", "progressive familial heart block type IA", "progressive familial heart block type 1A", "HEART BLOCK, PROGRESSIVE FAMILIAL, TYPE I", "Progressive Familial Heart Block, Type Ia", "Heart Block, Progressive Familial, Type I", "Cardiac conduction defect, nonprogressive", "Cardiac Conduction Defect, Nonprogressive", "PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA", "progressive familial heart block, type 1A", "heart block, progressive familial, type 1", "progressive familial heart block, type IA", "CARDIAC CONDUCTION DEFECT, NONPROGRESSIVE", "Progressive familial heart block, type IA", "Heart block, progressive familial, type 1", "Progressive familial heart block (disorder)", "Familial progressive cardiac conduction defect", "progressive familial heart block caused by mutation in SCN5A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive familial heart block, type 1A", "shortest_name_length": 4}
{"curie": "UMLS:C1142117", "names": ["Adnexa uteri pain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adnexa uteri pain", "shortest_name_length": 17}
{"curie": "MONDO:0015718", "names": ["mosaic trisomy 12", "Mosaic trisomy 12", "Trisomy 12 mosaicism", "trisomy 12 mosaicism", "Mosaic trisomy type 12", "Mosaic trisomy 12 syndrome", "Mosaic trisomy chromosome 12", "trisomy 12 mosaicism (diagnosis)", "Mosaic trisomy 12 syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mosaic trisomy 12", "shortest_name_length": 17}
{"curie": "MONDO:0017941", "names": ["CK", "CHIK", "chikungunya", "Chikungunya", "CHIKV infection", "Chikungunya Fever", "Chikungunya fever", "chikungunya fever", "Fever, Chikungunya", "Chikungunya; fever", "fever; Chikungunya", "Chickungunya Fever", "Chikungunya Fevers", "Fever, Chickungunya", "Chickungunya Fevers", "Chikungunya virus disease", "chikungunya viral disease", "Chikungunya Virus Infection", "Chikungunya virus infection", "Chikungunya Virus Infections", "arbovirus A Chikungunya type", "Infection, Chikungunya Virus", "Chikungunya fever (disorder)", "Chikungunya hemorrhagic fever", "Chikungunya haemorrhagic fever", "Chikungunya; hemorrhagic fever", "hemorrhagic fever; Chikungunya", "Chikungunya (hemorrhagic) fever", "infection due to Chikungunya virus", "Chikungunya virus infectious disease", "Chikungunya virus disease or disorder", "Mosquito-borne viral fever, Chikungunya", "Chikungunya hemorrhagic fever (diagnosis)", "Chikungunya virus caused disease or disorder", "infection due to Chikungunya virus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chikungunya", "shortest_name_length": 2}
{"curie": "UMLS:C5206838", "names": ["Malignant Retropharyngeal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Retropharyngeal Neoplasm", "shortest_name_length": 34}
{"curie": "UMLS:C0280400", "names": ["Stage IV Larynx Verrucous Carcinoma", "larynx verrucous carcinoma, stage IV", "Stage IV Laryngeal Verrucous Carcinoma", "larynx verrucous carcinoma, metastatic", "Laryngeal verrucous carcinoma stage IV", "Stage IV Verrucous Carcinoma of Larynx", "laryngeal verrucous carcinoma, stage IV", "laryngeal verrucous carcinoma, metastatic", "Stage IV Verrucous Carcinoma of the Larynx", "stage IV verrucous carcinoma of the larynx", "Stage IV Laryngeal Throat Verrucous Cancer", "verrucous carcinoma of the larynx, stage IV", "metastatic verrucous carcinoma of the larynx", "verrucous carcinoma of the larynx, metastatic", "Stage IV Laryngeal Verrucous Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laryngeal verrucous carcinoma stage IV", "shortest_name_length": 35}
{"curie": "UMLS:C0032319", "names": ["PNEUMOPERICARDIUM", "Pneumopericardium", "pneumopericardium", "Pneumopericardiums", "Pneumopericardium (disorder)", "pneumopericardium (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pneumopericardium", "shortest_name_length": 17}
{"curie": "UMLS:C1710125", "names": ["Solid Glomus Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Solid Glomus Tumor", "shortest_name_length": 18}
{"curie": "MONDO:0007597", "names": ["F8F9D", "FMFD II", "Factor VIII And Factor IX, Combined Deficiency", "factor 8 and Factor IX, combined deficiency of", "FACTOR VIII AND FACTOR IX, COMBINED DEFICIENCY OF", "familial multiple coagulation Factor deficiency 2", "factor VIII and Factor IX, combined deficiency of", "factor VIII and factor IX, combined deficiency OF", "Familial Multiple Coagulation Factor Deficiency II", "FAMILIAL MULTIPLE COAGULATION FACTOR DEFICIENCY II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "factor VIII and Factor IX, combined deficiency of", "shortest_name_length": 5}
{"curie": "UMLS:C0751709", "names": ["Multiple Peroxisomal Dysfunction", "Multiple Peroxisomal Dysfunctions", "Dysfunction, Multiple Peroxisomal", "Peroxisomal Dysfunction, Multiple", "Dysfunctions, Multiple Peroxisomal", "Peroxisomal Dysfunctions, Multiple", "Loss of multiple peroxisomal functions", "Loss of multiple peroxisomal functions (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peroxisomal Dysfunction, Multiple", "shortest_name_length": 32}
{"curie": "UMLS:C1611170", "names": ["Tumor perforation", "Tumour perforation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tumor perforation", "shortest_name_length": 17}
{"curie": "MONDO:0019520", "names": ["syndromic lymphedema", "syndrome associated with lymphedema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic lymphedema", "shortest_name_length": 20}
{"curie": "MONDO:0012475", "names": ["CDSRR", "RCD3B", "Retinal Cone Dystrophy 3B", "retinal cone dystrophy 3B", "RETINAL CONE DYSTROPHY 3B", "retinal cone dystrophy type 3B", "cone dystrophy with supernormal rod ERG", "Cone dystrophy with supernormal rod ERG", "cone dystrophy with supernormal rod response", "Cone dystrophy with supernormal rod response", "CONE DYSTROPHY WITH SUPERNORMAL ROD RESPONSES", "cone dystrophy with supernormal rod responses", "cone dystrophy with supernormal Rod responses", "cone dystrophy with supernormal rod electroretinogram", "Cone dystrophy with supernormal rod electroretinogram", "Cone dystrophy with supernormal rod response (disorder)", "cone dystrophy with supernormal scotopic electroretinogram", "Cone dystrophy with supernormal scotopic electroretinogram", "cone dystrophy with night blindness and supernormal rod responses KCNV2 related", "Cone Dystrophy with Night Blindness and Supernormal Rod Responses, KCNV2-Related", "CONE DYSTROPHY WITH NIGHT BLINDNESS AND SUPERNORMAL ROD RESPONSES, KCNV2-RELATED", "cone dystrophy with night blindness and supernormal Rod responses, Kcnv2-related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cone dystrophy with supernormal rod response", "shortest_name_length": 5}
{"curie": "UMLS:C0278726", "names": ["extensive stage SCLC", "Extensive Stage SCLC", "SCLC, extensive stage", "oat cell lung cancer, extensive stage", "extensive stage small cell lung cancer", "extensive-stage small cell lung cancer", "Small cell lung cancer extensive stage", "Extensive Stage Small Cell Lung Cancer", "Extensive Stage Oat Cell Lung Carcinoma", "small cell lung cancer, extensive stage", "Small Cell Lung Cancer, Extensive Stage", "lung cancer, extensive stage small cell", "Extensive Disease Small Cell Lung Cancer", "Extensive Stage Lung Small Cell Carcinoma", "Extensive Stage Small Cell Lung Carcinoma", "Extensive Stage Oat Cell Carcinoma of Lung", "Extensive Disease Small Cell Lung Carcinoma", "Extensive Stage Small Cell Carcinoma of Lung", "Extensive Stage Oat Cell Carcinoma of the Lung", "Extensive Stage Small Cell Carcinoma of the Lung", "small cell carcinoma of lung with extensive stage disease", "small cell carcinoma of lung with extensive stage disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small cell lung cancer extensive stage", "shortest_name_length": 20}
{"curie": "UMLS:C0751869", "names": ["Alcohol Withdrawal Induced Status Epilepticus", "Alcohol Withdrawal-Induced Status Epilepticus", "Status Epilepticus, Alcohol Withdrawal Induced", "Status Epilepticus, Alcohol Withdrawal-Induced"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Status Epilepticus, Alcohol Withdrawal-Induced", "shortest_name_length": 45}
{"curie": "UMLS:C0264558", "names": ["pneumothorax tension", "tension pneumothorax", "PNEUMOTHORAX TENSION", "Tension Pneumothorax", "Tension pneumothorax", "Pressure Pneumothorax", "Pneumothorax, Tension", "Pneumothorax, Pressure", "Tension pneumothorax (disorder)", "tension pneumothorax (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tension Pneumothorax", "shortest_name_length": 20}
{"curie": "UMLS:C4764228", "names": ["Refractory Fibrosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Fibrosarcoma", "shortest_name_length": 23}
{"curie": "MONDO:0002369", "names": ["Cystoma", "cystoma", "CYSTADENOMA", "cystadenoma", "Cystadenoma", "cystadenomas", "Cystoma, NOS", "Cystadenomas", "Cystadenoma NOS", "Cystadenoma, NOS", "[M]Cystadenoma NOS", "cystadenoma, benign", "CYSTADENOMA, BENIGN", "Cystadenoma (morphologic abnormality)", "cystadenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cystadenoma", "shortest_name_length": 7}
{"curie": "MONDO:0013605", "names": ["BCS2", "BRITTLE CORNEA SYNDROME 2", "brittle cornea syndrome 2", "PRDM5 brittle cornea syndrome", "brittle cornea syndrome type 2", "brittle cornea syndrome caused by mutation in PRDM5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brittle cornea syndrome 2", "shortest_name_length": 4}
{"curie": "UMLS:C2168280", "names": ["Appendix Leiomyosarcoma", "leiomyosarcoma of appendix", "leiomyosarcoma of appendix (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leiomyosarcoma of appendix", "shortest_name_length": 23}
{"curie": "UMLS:C1334720", "names": ["Metastatic MPNST", "Metastatic Malignant Peripheral Nerve Sheath Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Malignant Peripheral Nerve Sheath Tumor", "shortest_name_length": 16}
{"curie": "UMLS:C1403880", "names": ["meningoencephalitis viral", "viral meningoencephalitis", "Viral meningoencephalitis", "Meningoencephalitis viral", "virus; meningoencephalitis", "viral; meningoencephalitis", "meningoencephalitis; viral", "meningoencephalitis; virus", "Viral meningoencephalitis NOS", "Meningoencephalitis caused by virus", "viral meningoencephalitis (diagnosis)", "Meningoencephalitis caused by virus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meningoencephalitis caused by virus", "shortest_name_length": 25}
{"curie": "UMLS:C4553411", "names": ["IIA1", "Stage IIA1 Cervical Cancer", "Stage IIA1 Cervical Cancer AJCC v8", "Stage IIA1 Cervical Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA1 Cervical Cancer AJCC v8", "shortest_name_length": 4}
{"curie": "MONDO:0012732", "names": ["ETINPH", "TREMOR, HEREDITARY ESSENTIAL, AND IDIOPATHIC NORMAL PRESSURE HYDROCEPHALUS", "tremor, hereditary essential, and idiopathic normal pressure hydrocephalus", "Tremor, Hereditary Essential, And Idiopathic Normal Pressure Hydrocephalus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tremor, hereditary essential, and idiopathic normal pressure hydrocephalus", "shortest_name_length": 6}
{"curie": "UMLS:C0948205", "names": ["Enterobacter infection", "Enterobacter infections", "Infection caused by Enterobacter", "Infection caused by Enterobacter (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infection caused by Enterobacter", "shortest_name_length": 22}
{"curie": "UMLS:C4745370", "names": ["Adrenal Cortex Sex Cord-Stromal Tumor", "Adrenal Cortical Sex Cord-Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adrenal Cortical Sex Cord-Stromal Tumor", "shortest_name_length": 37}
{"curie": "MONDO:0012835", "names": ["SLEB11", "STAT4 systemic lupus erythematosus (disease)", "susceptibility to systemic lupus erythematosus 11", "SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 11", "systemic lupus erythematosus, susceptibility to, 11", "systemic lupus erythematosus, susceptibility to, type 11", "systemic lupus erythematosus (disease) caused by mutation in STAT4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "systemic lupus erythematosus, susceptibility to, 11", "shortest_name_length": 6}
{"curie": "UMLS:C0016542", "names": ["Foreign Body", "Foreign body", "FOREIGN BODY", "foreign body", "Body, Foreign", "Foreign Object", "Foreign object", "FOREIGN BODIES", "foreign bodies", "Foreign bodies", "Foreign Bodies", "Bodies, Foreign", "Object, Foreign", "Foreign Objects", "FOREIGN MATERIAL", "Objects, Foreign", "foreign material", "Foreign material", "FB - Foreign body", "Foreign body, NOS", "foreign materials", "Exogenous material", "Foreign material, NOS", "Foreign body (disorder)", "Foreign Body In Patient", "Exogenous material, NOS", "Foreign body of body structure", "FB - Foreign body of body structure", "Foreign body (morphologic abnormality)", "Disorder due to presence of foreign body"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Foreign Bodies", "shortest_name_length": 12}
{"curie": "UMLS:C4329652", "names": ["Cervical and Lumbosacral Spinal Cord Ependymal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical and Lumbosacral Spinal Cord Ependymal Tumor", "shortest_name_length": 52}
{"curie": "UMLS:C4316911", "names": ["Benign retention cyst", "ovary; cyst, retention", "Retention Ovarian Cyst", "Retention Cyst of Ovary", "Retention cyst of ovary", "Retention cyst of ovary NOS", "Retention Cyst of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign retention cyst", "shortest_name_length": 21}
{"curie": "MONDO:0009723", "names": ["LS", "LSS", "SNE", "Leigh", "leigh disease", "LEIGH DISEASE", "disease leigh", "Leigh disease", "Leigh Disease", "LEIGH SYNDROME", "Leigh Syndrome", "leighs disease", "Leighs Disease", "leigh syndrome", "Leigh syndrome", "Leighs disease", "diseases leighs", "leighs syndrome", "Leigh's Disease", "Leigh's disease", "leigh's disease", "Disease, Leigh's", "Leigh syndrome spectrum", "Leigh's disease (disorder)", "Leigh's disease (diagnosis)", "Leigh's necrotizing encephalopathy", "Subacute necrotising encephalopathy", "Subacute Necrotizing Encephalopathy", "Subacute necrotizing encephalopathy", "subacute necrotizing encephalopathy", "Encephalopathy, Subacute Necrotizing", "Necrotizing Encephalopathy, Subacute", "Subacute Necrotizing Encephalopathies", "Subacute Necrotizing Encephalomyelitis", "Necrotizing Encephalopathies, Subacute", "Encephalopathies, Subacute Necrotizing", "Necrotizing Encephalomyelitis, Subacute", "Encephalomyelitis, Subacute Necrotizing", "Subacute Necrotizing Encephalomyelitides", "Subacute necrotizing encephalomyelopathy", "Subacute necrotising encephalomyelopathy", "Subacute Necrotizing Encephalomyelopathy", "subacute necrotizing encephalomyelopathy", "infantile necrotizing encephalomyelopathy", "Necrotizing Encephalomyelopathy, Subacute", "Encephalomyelopathy, Subacute Necrotizing", "Necrotizing Encephalomyelitides, Subacute", "Infantile necrotizing encephalomyelopathy", "Encephalomyelitides, Subacute Necrotizing", "Infantile necrotising encephalomyelopathy", "Subacute Necrotizing Encephalomyelopathies", "ENCEPHALOMYELOPATHY, NECROTIZING, SUBACUTE", "Necrotizing Encephalomyelopathies, Subacute", "Encephalomyelopathies, Subacute Necrotizing", "Infantile subacute necrotizing encephalopathy", "infantile subacute necrotizing encephalopathy", "SNEM - Subacute necrotising encephalomyelopathy", "subacute necrotizing encephalopathy (diagnosis)", "SNEM - Subacute necrotizing encephalomyelopathy", "juvenile subacute necrotizing encephalomyelopathy", "infantile necrotizing encephalomyelopathy (diagnosis)", "Leigh syndrome due to mitochondrial Complex 1 deficiency", "NECROTIZING ENCEPHALOPATHY, INFANTILE SUBACUTE, OF LEIGH", "Leigh syndrome due to mitochondrial Complex 4 deficiency", "Leigh syndrome due to mitochondrial Complex 2 deficiency", "Leigh syndrome due to mitochondrial Complex 5 deficiency", "Leigh syndrome due to mitochondrial Complex 3 deficiency", "Necrotizing encephalopathy, infantile subacute, of Leigh", "necrotizing encephalopathy, infantile Subacute, of Leigh"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leigh syndrome", "shortest_name_length": 2}
{"curie": "UMLS:C0521554", "names": ["Congenital vesicoureteral reflux", "Congenital vesicoureteric reflux", "Congenital vesico-ureteric reflux", "reflux; vesicoureteral, congenital"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital vesico-ureteric reflux", "shortest_name_length": 32}
{"curie": "UMLS:C5556448", "names": ["sDNET", "DNET-Like Tumor of the Septum Pellucidum", "DNET-Like Neoplasm of the Septum Pellucidum", "Septal Dysembryoplastic Neuroepithelial Tumor", "Septal Dysembryoplastic Neuroepithelial Neoplasm", "Dysembryoplastic Neuroepithelial Tumor of the Septum Pellucidum", "Dysembryoplastic Neuroepithelial Neoplasm of the Septum Pellucidum", "Dysembryoplastic Neuroepithelial-Like Tumor of the Septum Pellucidum", "Dysembryoplastic Neuroepithelial-Like Neoplasm of the Septum Pellucidum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dysembryoplastic Neuroepithelial-Like Tumor of the Septum Pellucidum", "shortest_name_length": 5}
{"curie": "MONDO:0000962", "names": ["SCL", "spindle cell lipoma", "Spindle cell lipoma", "Spindle Cell Lipoma", "lipoma; spindle cell", "spindle cell; lipoma", "Spindle cell lipoma (disorder)", "Spindle cell lipoma (morphologic abnormality)", "spindle cell lipoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spindle cell lipoma", "shortest_name_length": 3}
{"curie": "UMLS:C3640143", "names": ["Stage II Differentiated Thyroid Gland Cancer 45 Years and Older", "Stage II Differentiated Thyroid Gland Carcinoma 45 Years and Older", "Stage II Differentiated Thyroid Gland Carcinoma 45 Years and Older AJCC v7", "Stage II Thyroid Gland Papillary or Follicular Carcinoma 45 Years and Older"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Differentiated Thyroid Gland Carcinoma 45 Years and Older AJCC v7", "shortest_name_length": 63}
{"curie": "UMLS:C0406815", "names": ["Sclerotic Fibroma", "Circumscribed Storiform Collagenoma", "Circumscribed storiform collagenoma", "Circumscribed storiform collagenoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Circumscribed storiform collagenoma", "shortest_name_length": 17}
{"curie": "UMLS:C0269899", "names": ["Early Postpartum Hemorrhage", "Atonic postpartum hemorrhage", "Primary postpartum hemorrhage", "Primary Postpartum Hemorrhage", "Atonic postpartum haemorrhage", "Primary postpartum haemorrhage", "Immediate Postpartum Hemorrhage", "Postpartum hemorrhage (primary)", "immediate postpartum hemorrhage", "Immediate postpartum hemorrhage", "Immediate postpartum haemorrhage", "Hemorrhage, Immediate Postpartum", "Postpartum Hemorrhage, Immediate", "Atonic postpartum hemorrhage NOS", "Postpartum haemorrhage (primary)", "Atonic postpartum hemorrhage, NOS", "Atonic postpartum haemorrhage, NOS", "Postpartum hemorrhage (atonic) NOS", "Atonic postpartum hemorrhage (disorder)", "postpartum hemorrhage due to atonic uterus", "immediate postpartum hemorrhage (diagnosis)", "immediate postpartum hemorrhage (within 24 hours)", "postpartum hemorrhage due to atonic uterus (diagnosis)", "Hemorrhage within 24 hours following delivery of placenta", "Haemorrhage within 24 hours following delivery of placenta", "Hemorrhage within the first 24 hours following delivery of placenta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immediate Postpartum Hemorrhage", "shortest_name_length": 27}
{"curie": "MONDO:0018694", "names": ["Tracheoesophageal Fistula", "tracheoesophageal fistula", "Tracheo-esophageal Fistula", "tracheo-esophageal fistula", "H-type tracheoesophageal fistula", "isolated tracheoesophageal fistula", "isolated tracheo-esophageal fistula"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated tracheo-esophageal fistula", "shortest_name_length": 25}
{"curie": "MONDO:0012838", "names": ["IBD16", "INFLAMMATORY BOWEL DISEASE 16", "Inflammatory Bowel Disease 16", "inflammatory bowel disease 16", "inflammatory bowel disease type 16"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory bowel disease 16", "shortest_name_length": 5}
{"curie": "MONDO:0009326", "names": ["congenital heart block", "Congenital heart block", "Heart block congenital", "HEART BLOCK, CONGENITAL", "Heart Block, Congenital", "heart block, congenital", "block; heart, congenital", "Congenital complete heart block", "Familial congenital heart block", "congenital atrioventricular block", "Congenital atrioventricular block", "Congenital heart block (disorder)", "congenital heart block (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital heart block", "shortest_name_length": 22}
{"curie": "UMLS:C2981370", "names": ["Stage IA Esophageal Adenocarcinoma", "Stage IA Esophageal Adenocarcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Esophageal Adenocarcinoma AJCC v7", "shortest_name_length": 34}
{"curie": "MONDO:0100031", "names": ["adolescent/adult onset autosomal dominant epilepsy with auditory features", "autosomal dominant partial/lateral temporal epilepsy with auditory features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adolescent/adult onset autosomal dominant epilepsy with auditory features", "shortest_name_length": 73}
{"curie": "MONDO:0017625", "names": ["familial primary hypomagnesemia with hypocalcuria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial primary hypomagnesemia with hypocalcuria", "shortest_name_length": 49}
{"curie": "UMLS:C0280468", "names": ["cancer of the renal pelvis and ureter, recurrent", "Recurrent Upper Urinary Tract Urothelial Carcinoma", "carcinoma of the renal pelvis and ureter, recurrent", "Recurrent Renal Pelvis and Ureter Urothelial Carcinoma", "Renal pelvis and ureter transitional cell cancer recurrent", "Recurrent Urothelial Cancer of the Renal Pelvis and Ureter", "Renal pelvis and ureteric cancer recurrent transitional cell", "Renal pelvis and ureteral cancer transitional cell recurrent", "Relapsed Transitional Cell Cancer of Renal Pelvis and Ureter", "Renal pelvis and ureteric cancer transitional cell recurrent", "Recurrent Transitional Cell Cancer of Renal Pelvis and Ureter", "Recurrent Urothelial Carcinoma of the Renal Pelvis and Ureter", "Relapsed Transitional Cell Carcinoma of Renal Pelvis and Ureter", "Relapsed Transitional Cell Cancer of the Renal Pelvis and Ureter", "Recurrent Transitional Cell Carcinoma of Renal Pelvis and Ureter", "recurrent transitional cell cancer of the renal pelvis and ureter", "Recurrent Transitional Cell Cancer of the Renal Pelvis and Ureter", "Transitional cell cancer of the renal pelvis and ureter recurrent", "transitional cell cancer of the renal pelvis and ureter, recurrent", "Relapsed Transitional Cell Carcinoma of the Renal Pelvis and Ureter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Urothelial Carcinoma of the Renal Pelvis and Ureter", "shortest_name_length": 48}
{"curie": "UMLS:C0160814", "names": ["Late Radiation Injury", "effects late radiation", "Late effect of radiation", "late effect of radiation", "late effects of radiation", "Delayed effect of radiation", "Delayed effects of radiation", "Late effect of radiation (disorder)", "late effects of radiation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Late effect of radiation", "shortest_name_length": 21}
{"curie": "MONDO:0005387", "names": ["POI", "POF", "premature menopause", "PRIMARY HYPOGONADISM", "primary hypogonadism", "HYPOGONADISM PRIMARY", "Primary hypogonadism", "Primary ovarian failure", "Ovarian failure primary", "Primary Gonadal Failure", "primary ovarian failure", "Primary gonadal failure", "primary gonadal failure", "Primary Ovarian Failure", "GONADAL FAILURE PRIMARY", "failure ovarian premature", "Premature Ovarian Failure", "Premature ovarian failure", "OVARIAN FAILURE PREMATURE", "premature ovarian failure", "Ovarian failure, premature", "OVARIAN FAILURE, PREMATURE", "Ovarian Failure, Premature", "primary female hypogonadism", "Primary female hypogonadism", "Primary ovarian failure NOS", "Primary Ovarian Insufficiency", "Primary ovarian insufficiency", "primary ovarian insufficiency", "Ovarian Insufficiency, Primary", "Hypergonadotropic Hypogonadism", "Hypergonadotropic hypogonadism", "hypergonadotropic hypogonadism", "Hypergonadotrophic hypogonadism", "premature ovarian insufficiency", "Hypogonadism, Hypergonadotropic", "POF - Premature ovarian failure", "Primary hypogonadism (disorder)", "hypergonadotrophic ovarian failure", "Primary ovarian failure (disorder)", "Hypergonadotrophic ovarian failure", "primary ovarian failure (diagnosis)", "Premature ovarian failure (disorder)", "female hypergonadotropic hypogonadism", "Female hypergonadotropic hypogonadism", "Hypergonadotropic Hypogonadism (Female)", "hypergonadotropic hypogonadism (female)", "Hypergonadotropic hypogonadism syndrome, female"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ovarian failure", "shortest_name_length": 3}
{"curie": "UMLS:C0334160", "names": ["Bridging Fibrosis", "Bridging fibrosis", "Bridging fibrosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bridging fibrosis", "shortest_name_length": 17}
{"curie": "UMLS:C0280304", "names": ["Retromolar Trigone Squamous Cell Carcinoma", "Squamous Cell Carcinoma of Retromolar Trigone", "Squamous Cell Carcinoma of the Retromolar Trigone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retromolar Trigone Squamous Cell Carcinoma", "shortest_name_length": 42}
{"curie": "UMLS:C0919568", "names": ["Impatience", "impatience"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Impatience", "shortest_name_length": 10}
{"curie": "MONDO:0000814", "names": ["adult B cell ALL", "B cell adult ALL", "B Cell Adult ALL", "B-cell adult ALL", "adult B-cell ALL", "B-Cell Adult ALL", "Adult B Cell ALL", "Adult B-Cell ALL", "ALL, adult B-cell", "adult ALL, B-cell", "ALL, adult B cell", "adult ALL, B cell", "B Acute Lymphoblastic Leukemia", "adult B-lymphoblastic leukemia", "B acute lymphoblastic leukemia", "adult B-lymphoblastic leukaemia", "adult b-cell lymphocytic leukemia", "adult B-cell lymphocytic leukemia", "adult b-cell lymphocytic leukaemia", "Adult B Acute Lymphoblastic Leukemia", "adult B acute lymphoblastic leukemia", "adult B acute lymphoblastic leukaemia", "B cell adult acute lymphocytic leukemia", "Adult B Cell Acute Lymphocytic Leukemia", "adult B cell acute lymphocytic leukemia", "B Cell Adult Acute Lymphocytic Leukemia", "B-Cell Adult Acute Lymphocytic Leukemia", "adult B-cell acute lymphocytic leukemia", "B-cell adult acute lymphocytic leukemia", "Adult B-Cell Acute Lymphocytic Leukemia", "B-cell acute lymphocytic leukemia, adult", "acute lymphocytic leukemia, adult B-cell", "B-cell lymphocytic leukemia, acute adult", "adult acute lymphocytic leukemia, B-cell", "B cell lymphocytic leukemia, acute adult", "adult precursor B-lymphoblastic leukemia", "Adult Precursor B-Lymphoblastic Leukemia", "B cell acute lymphocytic leukemia, adult", "B-cell adult acute lymphocytic leukaemia", "leukemia, adult acute lymphocytic B-cell", "B-cell adult acute lymphoblastic leukemia", "B-Cell Adult Acute Lymphoblastic Leukemia", "adult B cell acute lymphoblastic leukemia", "Adult B-Cell Acute Lymphoblastic Leukemia", "adult B-cell acute lymphoblastic leukemia", "adult b-cell acute lymphoblastic leukemia", "B cell adult acute lymphoblastic leukemia", "B Cell Adult Acute Lymphoblastic Leukemia", "Adult B Cell Acute Lymphoblastic Leukemia", "B-cell lymphoblastic leukemia, acute adult", "B-cell acute lymphoblastic leukemia, adult", "adult acute lymphoblastic leukemia, B-cell", "acute lymphoblastic leukemia, adult B-cell", "adult b-cell acute lymphoblastic leukaemia", "B cell adult acute lymphocytic leukemia, adult", "adult B-cell childhood acute lymphoblastic leukemia", "B-cell childhood acute lymphoblastic leukemia of adults"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-cell adult acute lymphocytic leukemia", "shortest_name_length": 16}
{"curie": "UMLS:C3272617", "names": ["Gastrointestinal NET G2", "Digestive System Neuroendocrine Tumor G2", "Gastrointestinal Neuroendocrine Tumor G2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Digestive System Neuroendocrine Tumor G2", "shortest_name_length": 23}
{"curie": "UMLS:C0003721", "names": ["Arboviral hemorrhagic fever", "Arbovirus hemorrhagic fever", "Arbovirus haemorrhagic fever", "hemorrhagic fever; arboviral", "Arboviral haemorrhagic fever", "arbovirus; hemorrhagic fever", "arbovirus; fever, hemorrhagic", "fever; arboviral, hemorrhagic", "Arbovirus hemorrhagic fever NOS", "Arbovirus hemorrhagic fever, NOS", "Arthropod-Borne Hemorrhagic Fever", "arthropod-borne hemorrhagic fever", "Arbovirus haemorrhagic fever, NOS", "Arthropod-borne hemorrhagic fever", "Arthropod-borne haemorrhagic fever", "Arbovirus hemorrhagic fever (disorder)", "Arthropod-borne hemorrhagic fever, NOS", "Arthropod-borne haemorrhagic fever, NOS", "arthropod-borne hemorrhagic fever (diagnosis)", "Arthropod-borne hemorrhagic fever, unspecified", "Arthropod-borne haemorrhagic fever, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arbovirus hemorrhagic fever", "shortest_name_length": 27}
{"curie": "MONDO:0016699", "names": ["Ependymoma benign", "ependymoma, benign", "EPENDYMOMA, BENIGN", "Myxopapillary Ependymoma", "myxopapillary ependymoma", "Myxopapillary ependymoma", "Myxopapillary Ependymomas", "Ependymoma, Myxopapillary", "ependymoma; myxopapillary", "Ependymomas, Myxopapillary", "ependymoma; myxopapillary, unspecified site", "myxopapillary; ependymoma, unspecified site", "myxopapillary ependymoma (morphologic abnormality)", "Myxopapillary ependymoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myxopapillary ependymoma", "shortest_name_length": 17}
{"curie": "UMLS:C1335011", "names": ["Non-Neoplastic Gastrointestinal Disorder", "Non-Neoplastic Digestive System Disorder", "Non-Neoplastic Gastrointestinal System Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Digestive System Disorder", "shortest_name_length": 40}
{"curie": "UMLS:C2062366", "names": ["Alpha Thalassemia Silent Carrier", "alpha-thalassemia silent carrier", "Alpha thalassemia silent carrier", "asymptomatic carrier of alpha-thalassemia", "asymptomatic carrier of alpha-thalassemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "asymptomatic carrier of alpha-thalassemia", "shortest_name_length": 32}
{"curie": "UMLS:C3642254", "names": ["High Grade Ovarian Serous Adenocarcinoma", "Ovarian High Grade Serous Adenocarcinoma", "ovarian adenocarcinoma serous high grade", "Ovarian High-Grade Serous Adenocarcinoma", "High-Grade Ovarian Serous Adenocarcinoma", "high grade serous adenocarcinoma of ovary", "high grade serous adenocarcinoma of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "high grade serous adenocarcinoma of ovary", "shortest_name_length": 40}
{"curie": "UMLS:C1858804", "names": ["Cerebellar Ataxia, Deafness, and Narcolepsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebellar Ataxia, Deafness, and Narcolepsy", "shortest_name_length": 43}
{"curie": "MONDO:0011451", "names": ["MC4DN2", "CEMCOX1", "SCO2 fatal infantile encephalocardiomyopathy", "mitochondrial complex IV deficiency nuclear type 2", "mitochondrial complex IV deficiency, nuclear type 2", "MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 2", "fatal infantile encephalocardiomyopathy caused by mutation in SCO2", "Cytochrome C Oxidase Deficiency, Fatal Infantile, with Cardioencephalomyopathy", "cytochrome C oxidase deficiency, fatal infantile, with cardioencephalomyopathy", "CYTOCHROME c OXIDASE DEFICIENCY, FATAL INFANTILE, WITH CARDIOENCEPHALOMYOPATHY", "Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency", "fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 1", "CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 1", "cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1", "cardioencephalomyopathy, fatal infantile, due to cytochrome C oxidase deficiency type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1", "shortest_name_length": 6}
{"curie": "UMLS:C0855074", "names": ["Recurrent Hodgkin's Disease Lymphocyte Predominance Type", "Hodgkin's disease lymphocyte predominance type recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's disease lymphocyte predominance type recurrent", "shortest_name_length": 56}
{"curie": "UMLS:C5555518", "names": ["Reaction to Injectable Product", "Injectable Product-Related Reaction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injectable Product-Related Reaction", "shortest_name_length": 30}
{"curie": "MONDO:0004140", "names": ["Intermediate Immature teratoma", "Intermediate immature teratoma", "Intermediate Immature Teratoma", "intermediate malignant teratoma", "malignant intermediate teratoma", "Intermediate Malignant Teratoma", "Malignant teratoma, intermediate", "malignant teratoma, intermediate", "Malignant teratoma - intermediate", "intermediate malignant teratoma (diagnosis)", "Malignant teratoma, intermediate (morphologic abnormality)", "malignant teratoma, intermediate (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intermediate malignant teratoma", "shortest_name_length": 30}
{"curie": "UMLS:C1334157", "names": ["Immunoblastic Lymphoma PTLD", "Immunoblastic Diffuse Large B-Cell Lymphoma PTLD", "Immunoblastic Lymphoma Post-Transplant Lymphoproliferative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immunoblastic Lymphoma Post-Transplant Lymphoproliferative Disorder", "shortest_name_length": 27}
{"curie": "MONDO:0002395", "names": ["adenoma renal", "Renal Adenoma", "renal adenoma", "Renal adenoma", "adenomas renal", "Kidney adenoma", "kidney adenoma", "Kidney Adenoma", "adenomas kidney", "adenoma of kidney", "renal cell adenoma", "Renal cell adenoma", "renal tubule adenoma", "Renal Tubule Adenoma", "adenoma, renal cell, benign", "ADENOMA, RENAL CELL, BENIGN", "adenoma of kidney (diagnosis)", "renal cell adenoma (morphologic abnormality)", "Renal cell adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal adenoma", "shortest_name_length": 13}
{"curie": "MONDO:0027029", "names": ["HHV-6 encephalitis", "Variant B or HHV-6B", "Variant A or HHV-6A", "Human Herpesvirus 6 encephalitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HHV-6 encephalitis", "shortest_name_length": 18}
{"curie": "MONDO:0014150", "names": ["EEOC", "DEE94", "CHCHD10-related disorders", "myoclonic-atonic epilepsy", "CHD2 myoclonic encephalopathy", "childhood onset epileptic encephalopathy", "childhood-onset epileptic encephalopathy", "Childhood-Onset Epileptic Encephalopathy", "epileptic encephalopathy, childhood-onset", "EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET", "developmental and epileptic encephalopathy 94", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 94"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy 94", "shortest_name_length": 4}
{"curie": "MONDO:0000590", "names": ["peripheral nervous system autoimmune disease", "autoimmune disease of peripheral nervous system", "autoimmune disorder of peripheral nervous system", "peripheral nervous system hypersensitivity reaction type II disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune disorder of peripheral nervous system", "shortest_name_length": 44}
{"curie": "MONDO:0004324", "names": ["fibroma of testis", "testicular fibroma", "Testicular Fibroma", "fibroma of testis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular fibroma", "shortest_name_length": 17}
{"curie": "MONDO:0005012", "names": ["CM", "CMM", "Famm", "SKIN MELANOMA", "melanoma skin", "Melanoma skin", "Skin Melanoma", "Skin melanoma", "MELANOMA SKIN", "skin melanoma", "skin melanomas", "skin; melanoma", "melanoma; skin", "skin, melanoma", "Skin, Melanoma", "Melanoma of skin", "melanoma of skin", "Melanoma of Skin", "Melanomas of skin", "melanomas of skin", "Melanoma, Familial", "cutaneous melanoma", "Cutaneous melanoma", "Cutaneous Melanoma", "melanoma, cutaneous", "MELANOMA, MALIGNANT", "melanoma skin cancer", "skin cancer melanoma", "skin melanoma cancer", "melanoma of the skin", "Melanoma of the Skin", "cancer melanoma skin", "SKIN CANCER, MELANOMA", "zone of skin melanoma", "Skin cancer, melanoma", "Skin cancer (melanoma)", "malignant ear melanoma", "malignant lip melanoma", "malignant neck melanoma", "skin malignant melanoma", "Skin cancers - melanoma", "malignant melanoma skin", "malignant trunk melanoma", "Melanoma (malignant) NOS", "malignant scalp melanoma", "cutaneous (skin) melanoma", "Cutaneous (Skin) Melanoma", "malignant melanoma of skin", "Malignant melanoma of skin", "Malignant Melanoma of Skin", "Melanoma of skin (disorder)", "malignant cutaneous melanoma", "cutaneous melanoma (disease)", "Melanoma of skin (malignant)", "Malignant Cutaneous Melanoma", "cutaneous malignant melanoma", "Cutaneous malignant melanoma", "malignant upper limb melanoma", "Melanoma, Cutaneous Malignant", "MELANOMA, CUTANEOUS MALIGNANT", "malignant lower limb melanoma", "SKIN CANCER MALIGNANT MELANOMA", "MM - Malignant melanoma of skin", "Malignant melanoma of skin, NOS", "zone of skin melanoma (disease)", "MM (malignant melanoma) of skin", "malignant melanoma of lower limb", "melanoma (disease) of zone of skin", "Melanoma of skin, site unspecified", "Dysplastic Nevus Syndrome, Hereditary", "malignant melanoma of lower extremity", "Malignant melanoma of skin (disorder)", "malignant melanoma of skin (diagnosis)", "Malignant melanoma of skin, unspecified", "Malignant melanoma of skin of lower limb", "malignant melanoma of skin of upper limb", "Malignant melanoma of skin of upper limb", "malignant melanoma of skin of lower limb", "Malignant melanoma of skin stage unspecified", "Malignant Melanoma of Skin Stage Unspecified", "malignant melanoma of skin stage unspecified", "malignant melanoma of lower limb (diagnosis)", "Malignant melanoma of skin of upper limb, NOS", "Malignant melanoma of skin of lower limb, NOS", "malignant melanoma (of skin), stage unspecified", "Malignant Melanoma (of Skin), Stage Unspecified", "Familial Atypical Mole-Malignant Melanoma Syndrome", "malignant melanoma of skin of trunk except scrotum", "Malignant melanoma of skin of upper limb (disorder)", "Malignant melanoma of skin of lower limb (disorder)", "malignant melanoma of ear and/or external auricular canal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous melanoma", "shortest_name_length": 2}
{"curie": "EFO:0009523", "names": ["fecal incontinence"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fecal incontinence", "shortest_name_length": 18}
{"curie": "UMLS:C5418756", "names": ["Metastatic Malignant Breast Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Malignant Breast Neoplasm", "shortest_name_length": 36}
{"curie": "UMLS:C1334176", "names": ["Inferior Vena Cava Leiomyosarcoma", "Leiomyosarcoma of Inferior Vena Cava", "Leiomyosarcoma of the Inferior Vena Cava"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Inferior Vena Cava Leiomyosarcoma", "shortest_name_length": 33}
{"curie": "UMLS:C5419871", "names": ["Unresectable Large Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Large Cell Neuroendocrine Carcinoma", "shortest_name_length": 48}
{"curie": "MONDO:0010288", "names": ["adrenomyodystrophy", "ADRENOMYODYSTROPHY", "Adrenomyodystrophy", "x-linked adrenomyodystrophy", "Adrenomyodystrophy (disorder)", "Adrenomyodystrophy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adrenomyodystrophy", "shortest_name_length": 18}
{"curie": "MONDO:0004376", "names": ["Nipple Syringomatous Tumor", "Nipple Syringomatous Adenoma", "nipple syringomatous adenoma", "Syringomatous tumor of nipple", "Syringomatous tumour of nipple", "Syringomatous adenoma of nipple", "Syringomatous Tumor of the Nipple", "infiltrating nipple syringomatous adenoma", "Infiltrating Nipple Syringomatous Adenoma", "Infiltrating syringomatous adenoma of nipple", "Syringomatous tumor of nipple (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infiltrating nipple syringomatous adenoma", "shortest_name_length": 26}
{"curie": "MONDO:0015809", "names": ["Pagetoid reticulosis", "Pagetoid Reticuloses", "pagetoid reticulosis", "Pagetoid Reticulosis", "localized reticulosis", "Reticulosis, Pagetoid", "Reticuloses, Pagetoid", "localised reticulosis", "Woringer-Kolopp Disease", "Woringer Kolopp Disease", "Disease, Woringer-Kolopp", "Kolopp Disease, Woringer", "Disease, Woringer Kolopp", "Epidermotropic reticulosis", "Epidermotropic lymphoblastoma", "localized pagetoid reticulosis", "Localized pagetoid reticulosis", "Localised pagetoid reticulosis", "Pagetoid reticulosis (disorder)", "pagetoid reticulosis (diagnosis)", "Localized pagetoid reticulosis (disorder)", "localized pagetoid reticulosis (diagnosis)", "Pagetoid reticulosis, Woringer-Kolopp type", "pagetoid reticulosis, Woringer-Kolopp type", "Pagetoid reticulosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "localized pagetoid reticulosis", "shortest_name_length": 20}
{"curie": "MONDO:0013013", "names": ["QME", "AURICULAR CLEFT, CONGENITAL", "auricular cleft, congenital", "QUESTION MARK EARS, ISOLATED", "question MARK ears, isolated", "question mark ears, isolated", "Cosman deformity of the auricle", "COSMAN DEFORMITY OF THE AURICLE", "EARS, PROMINENT AND CONSTRICTED", "ears, prominent and constricted"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "question mark ears, isolated", "shortest_name_length": 3}
{"curie": "MONDO:0020817", "names": ["Miliaria vesiculosa", "miliaria vesiculosa", "Miliaria vesiculosa (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "miliaria vesiculosa", "shortest_name_length": 19}
{"curie": "MONDO:0017691", "names": ["erythrocyte GALE-D", "Erythrocyte GALE-D", "Erythrocyte GALE deficiency", "erythrocyte GALE deficiency", "Erythrocyte galactose epimerase deficiency", "erythrocyte galactose epimerase deficiency", "erythrocyte epimerase deficiency galactosemia", "Erythrocyte epimerase deficiency galactosemia", "Erythrocyte UDP-galactose-4-epimerase deficiency", "erythrocyte UDP-galactose-4-epimerase deficiency", "erythrocyte uridine diphosphate galactose-4-epimerase deficiency", "Erythrocyte uridine diphosphate galactose-4-epimerase deficiency", "Erythrocyte uridine diphosphate galactose-4-epimerase deficiency (disorder)", "Erythrocyte uridine diphosphate galactose-4-epimerase deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythrocyte galactose epimerase deficiency", "shortest_name_length": 18}
{"curie": "MONDO:0017354", "names": ["infantile NKH", "infantile glycine encephalopathy", "glycine encephalopathy of infancy", "infantile non-ketotic hyperglycinemia", "infantile onset glycine encephalopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile glycine encephalopathy", "shortest_name_length": 13}
{"curie": "UMLS:C0154640", "names": ["Meningitis staphylococcal", "staphylococcal meningitis", "meningitis staphylococcal", "Staphylococcal meningitis", "staphylococcal; meningitis", "meningitis; staphylococcal", "Staphylococcal meningitis (disorder)", "Staphylococcal meningitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Staphylococcal meningitis", "shortest_name_length": 25}
{"curie": "UMLS:C0280402", "names": ["Relapsed Larynx Verrucous Carcinoma", "Recurrent Larynx Verrucous Carcinoma", "larynx verrucous carcinoma, recurrent", "Relapsed Laryngeal Verrucous Carcinoma", "Relapsed Verrucous Carcinoma of Larynx", "Laryngeal verrucous carcinoma recurrent", "Recurrent Laryngeal Verrucous Carcinoma", "Recurrent Verrucous Carcinoma of Larynx", "laryngeal verrucous carcinoma, recurrent", "Relapsed Verrucous Carcinoma of the Larynx", "Recurrent Laryngeal Throat Verrucous Cancer", "Recurrent Verrucous Carcinoma of the Larynx", "recurrent verrucous carcinoma of the larynx", "verrucous carcinoma of the larynx, recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laryngeal verrucous carcinoma recurrent", "shortest_name_length": 35}
{"curie": "MONDO:0017463", "names": ["congenital pseudarthrosis of the femur", "congenital pseudoarthrosis of the femur"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital pseudoarthrosis of the femur", "shortest_name_length": 38}
{"curie": "UMLS:C3272422", "names": ["Gastric Gastrointestinal Stromal Tumor of Uncertain Malignant Potential"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Gastrointestinal Stromal Tumor of Uncertain Malignant Potential", "shortest_name_length": 71}
{"curie": "MONDO:0700127", "names": ["mosaic trisomy 21"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mosaic trisomy 21", "shortest_name_length": 17}
{"curie": "MONDO:0044643", "names": ["congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome", "congenital agenesis of labia majora or scrotum-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome", "shortest_name_length": 102}
{"curie": "MONDO:0012490", "names": ["CRSD", "CSNB2B", "CSNB2B, FORMERLY", "CSNB, Incomplete, Autosomal Recessive", "Night Blindness, Congenital Stationary, Type 2B", "congenital stationary night blindness - type 2b", "night blindness, congenital stationary, type 2B", "CONE-ROD SYNAPTIC DISORDER, CONGENITAL NONPROGRESSIVE", "Cone-rod synaptic disorder, congenital nonprogressive", "cone-rod synaptic disorder, congenital nonprogressive", "NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B, FORMERLY", "night blindness, congenital stationary, type 2B, formerly", "NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder)", "congenital stationary night blindness - type 2b (diagnosis)", "night blindness, congenital stationary, incomplete, autosomal recessive", "Night Blindness, Congenital Stationary, Incomplete, Autosomal Recessive", "NIGHT BLINDNESS, CONGENITAL STATIONARY, INCOMPLETE, AUTOSOMAL RECESSIVE, FORMERLY", "night blindness, congenital stationary, incomplete, autosomal recessive, formerly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cone-rod synaptic disorder, congenital nonprogressive", "shortest_name_length": 4}
{"curie": "MONDO:0008993", "names": ["CLEFT PALATE, DEAFNESS, AND OLIGODONTIA", "Cleft Palate, Deafness, and Oligodontia", "cleft palate, deafness, and oligodontia", "cleft palate stapes fixation oligodontia", "cleft palate-stapes fixation-oligodontia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleft palate-stapes fixation-oligodontia syndrome", "shortest_name_length": 39}
{"curie": "MONDO:0016483", "names": ["Familial berry aneurysm", "familial berry aneurysm", "saccular cerebral aneurysm", "intracranial berry aneurysm", "aneurysm, intracranial berry", "Familial cerebral saccular aneurysm", "familial cerebral saccular aneurysm", "Familial intracranial saccular aneurysm", "familial intracranial saccular aneurysm", "familial aneurysmal subarachnoid hemorrhage", "Familial cerebral saccular aneurysm (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intracranial berry aneurysm", "shortest_name_length": 23}
{"curie": "MONDO:0015912", "names": ["May", "SBS", "MHA", "FTNS", "MYH9RD", "BDPLT6", "matins", "MATINS", "EPSTNS", "MYH9-RD", "APSM, FORMERLY", "Epstein syndrome", "Epstein Syndrome", "EPSTEIN SYNDROME", "epstein syndrome", "Fechtner Syndrome", "FECHTNER SYNDROME", "Fechtner syndrome", "Epstein's syndrome", "epstein's syndrome", "Sebastian syndrome", "SEBASTIAN SYNDROME", "May-Hegglin anomaly", "MAY-HEGGLIN ANOMALY", "Fechtner's syndrome", "May-Hegglin Anomaly", "May Hegglin syndrome", "anomaly; May-Hegglin", "May-Heggalin anomaly", "May-Hegglin syndrome", "May-Hegglin; anomaly", "MYH9-related disease", "MYH9 related disease", "MYH9-Related Disease", "MYH-9 related disease", "MYH9-related disorder", "Myh9-Related Disorder", "MYH9-related syndrome", "MYH9-Related Disorders", "MYH9 related disorders", "Epstein syndrome (disorder)", "SEBASTIAN PLATELET SYNDROME", "Sebastian platelet syndrome", "May-Hegglin thrombocytopenia", "Fechtner syndrome (disorder)", "Epstein syndrome (diagnosis)", "Brodie Chole griffin syndrome", "Brodie Chole Griffin syndrome", "Fechtner syndrome (diagnosis)", "MYH9 related thrombocytopenia", "May-Hegglin anomaly (diagnosis)", "BLEEDING DISORDER, PLATELET-TYPE, 6", "Myh9-Related Macrothrombocytopenias", "bleeding disorder, Platelet-type, 6", "MYH9-related syndromic thrombocytopenia", "Epstein's macrothrombocytopenia syndrome", "Autosomal Dominant Myh9 Spectrum Disorders", "Alport syndrome with macrothrombocytopenia", "macrothrombocytopenia progressive deafness", "Macrothrombocytopenia progressive deafness", "giant platelet syndrome with thrombocytopenia", "Giant Platelet Syndrome with Thrombocytopenia", "GIANT PLATELET SYNDROME WITH THROMBOCYTOPENIA", "MACROTHROMBOCYTOPENIA, NEPHRITIS, AND DEAFNESS", "macrothrombocytopenia, nephritis, and deafness", "Macrothrombocytopathy, Nephritis, and Deafness", "DOHLE LEUKOCYTE INCLUSIONS WITH GIANT PLATELETS", "MACROTHROMBOCYTOPENIA WITH LEUKOCYTE INCLUSIONS", "Macrothrombocytopenia with leukocyte inclusions", "macrothrombocytopenia with leukocyte inclusions", "Myosin heavy chain 9 non muscle related disease", "Dohle leukocyte inclusions with giant platelets", "MYH9 Gene-Related Autosomal Macrothrombocytopenias", "ALPORT SYNDROME WITH MACROTHROMBOCYTOPENIA, FORMERLY", "Alport syndrome with macrothrombocytopenia, formerly", "Myosin heavy chain 9 non muscle related disease (disorder)", "macrothrombocytopenia with dispersed leukocytic inclusions", "MACROTHROMBOCYTOPENIA WITH DISPERSED LEUKOCYTIC INCLUSIONS", "macrothrombocytopenia and progressive sensorineural deafness", "MACROTHROMBOCYTOPENIA AND PROGRESSIVE SENSORINEURAL DEAFNESS", "Macrothrombocytopenia and Progressive Sensorineural Deafness", "Alport Syndrome with Leukocyte Inclusions and Macrothrombocytopenia", "Macrothrombocytopathy, nephritis, deafness, and leukocyte inclusions", "MACROTHROMBOCYTOPENIA, NEPHRITIS, DEAFNESS, AND LEUKOCYTE INCLUSIONS", "macrothrombocytopenia, nephritis, deafness, and leukocyte inclusions", "Macrothrombocytopenia and Granulocyte Inclusions with or without Nephritis or Sensorineural Hearing Loss", "macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss", "MACROTHROMBOCYTOPENIA AND GRANULOCYTE INCLUSIONS WITH OR WITHOUT NEPHRITIS OR SENSORINEURAL HEARING LOSS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss", "shortest_name_length": 3}
{"curie": "UMLS:C5670671", "names": ["Stage IA2 Cervical Cancer FIGO 2009", "Stage IA2 Cervical Carcinoma FIGO 2009"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA2 Cervical Cancer FIGO 2009", "shortest_name_length": 35}
{"curie": "MONDO:0010302", "names": ["Ito", "HMI", "IPA", "Ito's nevus", "hi syndrome", "nevus of Ito", "Ito hypomelanosis", "hypomelanosis of Ito", "Bloch-Siemans syndrome", "Incontinentia pigmenti type 1", "pigmentary mosaicism, Ito type", "Incontinentia pigmenti, type I", "Incontinentia pigmenti achromians", "incontinentia pigmenti achromians", "Incontinentia pigmenti type 1 (formerly)", "Incontinentia pigmenti, type I, formerly", "Incontinentia pigmenti achromians syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ito hypomelanosis", "shortest_name_length": 3}
{"curie": "MONDO:0016384", "names": ["Salti-Salem syndrome", "Salti Salem syndrome", "hypogonadotropic hypogonadism-frontoparietal alopecia syndrome", "Hypogonadotropic hypogonadism-frontoparietal alopecia syndrome", "Hypogonadotropic hypogonadism with frontoparietal alopecia syndrome", "Hypogonadotropic hypogonadism with frontoparietal alopecia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadotropic hypogonadism-frontoparietal alopecia syndrome", "shortest_name_length": 20}
{"curie": "UMLS:C1168206", "names": ["Stage IVB Pancreatic Cancer", "Pancreatic Cancer Stage IVB", "stage IVB pancreatic cancer", "pancreatic cancer, stage IVB", "Stage IVB Pancreatic Carcinoma", "Pancreatic carcinoma stage IVB", "Stage IVB Carcinoma of Pancreas", "Stage IVB Carcinoma of the Pancreas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Pancreatic Cancer", "shortest_name_length": 27}
{"curie": "MONDO:0013186", "names": ["NS6", "Noonan syndrome 6", "NOONAN SYNDROME 6", "Noonan Syndrome 6", "NRAS Noonan syndrome", "Noonan syndrome type 6", "NRAS gene related Noonan syndrome", "Noonan syndrome caused by mutation in NRAS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Noonan syndrome 6", "shortest_name_length": 3}
{"curie": "MONDO:0018607", "names": ["CHR-RPE", "combined hamartoma of the retina and RPE", "Combined hamartoma of the retina and RPE", "Combined hamartoma of retina and retinal pigment epithelium", "Combined Hamartoma of the Retina and Retinal Pigment Epithelium", "Combined hamartoma of the retina and retinal pigment epithelium", "combined hamartoma of the retina and retinal pigment epithelium", "Combined hamartoma of the retinal pigment epithelium and retina", "CHR-RPE - combined hamartoma of retina and retinal pigment epithelium", "Combined hamartoma of retina and retinal pigment epithelium (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined hamartoma of the retina and retinal pigment epithelium", "shortest_name_length": 7}
{"curie": "MONDO:0018969", "names": ["CRANIORACHISCHISIS", "Craniorachischises", "craniorachischisis", "Craniorachischisis", "cranial rachischisis", "Cranial Rachischisis", "craniorachischisis (disease)", "Craniorachischisis (disorder)", "craniorachischisis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniorachischisis", "shortest_name_length": 18}
{"curie": "MONDO:0003245", "names": ["aflatoxins-related hepatocellular cancer", "Aflatoxins-Related Hepatocellular Cancer", "aflatoxin-related hepatocellular carcinoma", "aflatoxins-related hepatocellular carcinoma", "Aflatoxins-Related Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aflatoxin-related hepatocellular carcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0017172", "names": ["MPS6, slowly progressing", "MPSVI, slowly progressing", "arylsulfatase B deficiency, slowly progressing", "mucopolysaccharidosis type 6, slowly progressing", "mucopolysaccharidosis type VI, slowly progressing"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucopolysaccharidosis type 6, slowly progressing", "shortest_name_length": 24}
{"curie": "MONDO:0033630", "names": ["NEDSID", "NEURODEVELOPMENTAL DISORDER WITH SPEECH IMPAIRMENT AND DYSMORPHIC FACIES", "neurodevelopmental disorder with speech impairment and dysmorphic facies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with speech impairment and dysmorphic facies", "shortest_name_length": 6}
{"curie": "MONDO:0013103", "names": ["EJM7", "GEFS5", "EIG10", "GEFSP5, SUSCEPTIBILITY TO", "GEFS+5, SUSCEPTIBILITY TO", "GEFSP5, susceptibility to", "GEFS+5, susceptibility to", "GEFS+, TYPE 5, SUSCEPTIBILITY TO", "GEFS+, type 5, susceptibility to", "idiopathic generalized epilepsy 10", "epilepsy, idiopathic generalized, 10", "epilepsy, juvenile myoclonic, susceptibility to", "epilepsy, juvenile myoclonic, susceptibility to, 7", "EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 7", "susceptibility to idiopathic generalized epilepsy 10", "EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 10", "epilepsy, idiopathic generalized, susceptibility to, 10", "epilepsy, idiopathic generalized, susceptibility to, type 10", "generalized epilepsy with febrile seizures plus, type 5, susceptibility to", "GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 5, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, idiopathic generalized, susceptibility to, 10", "shortest_name_length": 4}
{"curie": "UMLS:C0153027", "names": ["Herpes zoster keratoconjunctivitis", "Herpes zoster with keratoconjunctivitis", "Herpes zoster keratoconjunctivitis (disorder)", "Herpes zoster keratoconjunctivitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Herpes zoster keratoconjunctivitis", "shortest_name_length": 34}
{"curie": "MONDO:0004964", "names": ["PTCL", "Peripheral T-Cell Lymphoma, NOS", "Peripheral T-cell lymphoma, NOS", "unspecified peripheral T-cell lymphoma", "Peripheral T-Cell Lymphoma, Not Otherwise Specified", "peripheral T-cell lymphoma, not otherwise specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peripheral T-cell lymphoma, not otherwise specified", "shortest_name_length": 4}
{"curie": "MONDO:0013828", "names": ["HKPX2", "HYPEREKPLEXIA 2", "hyperekplexia 2", "hyperekplexia type 2", "GLRB hereditary hyperekplexia", "hereditary hyperekplexia caused by mutation in GLRB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperekplexia 2", "shortest_name_length": 5}
{"curie": "UMLS:C0376288", "names": ["Amaurosis", "AMAUROSIS", "amaurosis", "Amauroses", "Amaurosis, NOS", "Amaurosis (disorder)", "amaurosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Amaurosis", "shortest_name_length": 9}
{"curie": "MONDO:0018160", "names": ["RB1", "Familial Retinoblastoma", "familial retinoblastoma", "Familial Retinoblastomas", "Retinoblastoma, Familial", "Retinoblastomas, Familial", "Hereditary Retinoblastoma", "Hereditary retinoblastoma", "hereditary retinoblastoma", "retinoblastoma, hereditary", "Retinoblastoma, Hereditary", "Hereditary Retinoblastomas", "Retinoblastomas, Hereditary", "retinoblastoma, autosomal dominant, somatic mutation", "retinoblastoma, trilateral, autosomal dominant, somatic mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary retinoblastoma", "shortest_name_length": 3}
{"curie": "MONDO:0003755", "names": ["non-invasive urothelial neoplasm", "Non-Invasive Urothelial Neoplasm", "urinary tract non-invasive transitional cell neoplasm", "Non-Invasive Transitional Cell Neoplasm of the Urinary Tract", "non-invasive transitional cell neoplasm of the urinary tract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urinary tract non-invasive transitional cell neoplasm", "shortest_name_length": 32}
{"curie": "UMLS:C0153702", "names": ["RETICULOSARCOMA SPLEEN", "Reticulosarcoma, spleen", "Reticulosarcoma of spleen", "Reticulosarcoma Involving Spleen", "Reticulosarcoma involving spleen", "Reticulosarcoma of spleen (disorder)", "Reticulosarcoma of spleen (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reticulosarcoma of spleen", "shortest_name_length": 22}
{"curie": "MONDO:0030750", "names": ["JEB4", "GABEB", "epidermolysis bullosa, junctional 4, intermediate", "EPIDERMOLYSIS BULLOSA, JUNCTIONAL 4, INTERMEDIATE", "epidermolysis bullosa, generalized atrophic benign", "EPIDERMOLYSIS BULLOSA, GENERALIZED ATROPHIC BENIGN", "epidermolysis bullosa, junctional 4, non-herlitz IIA", "Epidermolysis Bullosa, Junctional, Localisata Variant", "EPIDERMOLYSIS BULLOSA, JUNCTIONAL 4, NON-HERLITZ TYPE", "EPIDERMOLYSIS BULLOSA, JUNCTIONAL, LOCALISATA VARIANT", "epidermolysis bullosa, junctional, localisata variant", "EPIDERMOLYSIS BULLOSA, JUNCTIONAL, LOCALISATA VARIANT (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolysis bullosa, junctional 4, intermediate", "shortest_name_length": 4}
{"curie": "UMLS:C1710249", "names": ["Superficial Epithelioma with Sebaceous Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Superficial Epithelioma with Sebaceous Differentiation", "shortest_name_length": 54}
{"curie": "UMLS:C2987226", "names": ["Pancreatic Teratoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Teratoma", "shortest_name_length": 19}
{"curie": "MONDO:0008706", "names": ["Ackerman syndrome", "ACKERMAN SYNDROME", "Ackerman syndrome (disorder)", "Ackerman fused molar roots syndrome", "Ackerman fused molar rooth syndrome", "Pyramidal molars-abnormal upper lip syndrome", "Pyramidal molars, glaucoma, abnormal upper lip", "pyramidal molars, glaucoma, abnormal upper lip", "pyramidal molar-glaucoma-upper abnormal lip syndrome", "juvenile glaucoma with unusual upper lip and dental roots", "Juvenile glaucoma with unusual upper lip and dental roots", "glaucoma, juvenile, with unusual upper lip and dental roots", "Glaucoma, Juvenile, With Unusual Upper Lip And Dental Roots", "GLAUCOMA, JUVENILE, WITH UNUSUAL UPPER LIP AND DENTAL ROOTS", "molar roots, pyramidal, with juvenile glaucoma and unusual upper lip", "Molar Roots, Pyramidal, With Juvenile Glaucoma And Unusual Upper Lip", "MOLAR ROOTS, PYRAMIDAL, WITH JUVENILE GLAUCOMA AND UNUSUAL UPPER LIP"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ackerman syndrome", "shortest_name_length": 17}
{"curie": "MONDO:0004379", "names": ["Carcinoma;breast;F", "female breast cancer", "Female breast cancer", "Female Breast Cancer", "Breast cancer female", "breast cancer female", "Breast cancer, female", "Neoplasm malig;breast;F", "female breast carcinoma", "carcinoma of the breast", "Female Breast Carcinoma", "cancer of female breast", "Cancer of female breast", "breast carcinoma, female", "Breast cancer female NOS", "Breast Carcinoma, Female", "carcinoma of female breast", "CARCINOMA OF FEMALE BREAST", "Carcinoma of female breast", "Carcinoma of Female Breast", "Carcinoma of the Female Breast", "carcinoma of the female breast", "malignant tumor of female breast", "malignant female breast neoplasm", "BREAST NEOPLASM MALIGNANT FEMALE", "malignant neoplasm female breast", "Malignant neoplasm breast female", "Breast neoplasm malignant female", "Mammary Carcinoma of Female Breast", "Mammary carcinoma of female breast", "mammary carcinoma of female breast", "Malignant neoplasm of female breast", "malignant neoplasm of female breast", "Carcinoma of female breast (diagnosis)", "mammary carcinoma of the female breast", "Mammary Carcinoma of the Female Breast", "malignant neosplasm of the female breast", "Malignant neoplasm of female breast, NOS", "breast neoplasm malignant female carcinoma", "Malignant neoplasm of female breast (disorder)", "Malignant epithelial neoplasm of female breast", "malignant neoplasm of female breast (diagnosis)", "Malignant neoplasm of female breast, unspecified", "Malignant neoplasm of breast (female), unspecified", "Malignant epithelial neoplasm of female breast (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "female breast carcinoma", "shortest_name_length": 18}
{"curie": "UMLS:C4331762", "names": ["Wolff-Chaikoff", "Wolff-Chaikoff Phenomenon", "Wolff-Chaikoff Syndrome/Phenomenon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wolff-Chaikoff Phenomenon", "shortest_name_length": 14}
{"curie": "UMLS:C2981278", "names": ["Stage IVC Thyroid Gland Anaplastic Carcinoma AJCC v7", "Undifferentiated (Anaplastic) Stage IVC Thyroid Gland Cancer", "Stage IVC Thyroid Gland Undifferentiated (Anaplastic) Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Thyroid Gland Undifferentiated (Anaplastic) Carcinoma AJCC v7", "shortest_name_length": 52}
{"curie": "MONDO:0001543", "names": ["sciatic lesion nerve", "Sciatic Nerve Lesion", "Sciatic nerve lesion", "sciatic nerve lesion", "Sciatic Nerve Lesions", "Nerve Lesion, Sciatic", "n.ischiadicus; lesion", "lesion; sciatic nerve", "Nerve Lesions, Sciatic", "Lesion of sciatic nerve", "Lesion of Sciatic Nerve", "lesion of sciatic nerve", "Sciatic nerve lesion NOS", "Lesion of sciatic nerve, NOS", "Sciatic nerve lesion (disorder)", "sciatic nerve peripheral nerve lesion", "peripheral nerve lesion of sciatic nerve", "Lesion of sciatic nerve, unspecified lower limb"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lesion of sciatic nerve", "shortest_name_length": 20}
{"curie": "UMLS:C5447696", "names": ["SCD34FT", "Superficial CD34-Positive Fibroblastic Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Superficial CD34-Positive Fibroblastic Tumor", "shortest_name_length": 7}
{"curie": "MONDO:0013307", "names": ["MLASA2", "myopathy, lactic acidosis, and sideroblastic anemia 2", "MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 2", "YARS2 mitochondrial myopathy and sideroblastic anemia", "myopathy, lactic acidosis, and sideroblastic Anemia type 2", "mitochondrial myopathy and sideroblastic anemia caused by mutation in YARS2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy, lactic acidosis, and sideroblastic anemia 2", "shortest_name_length": 6}
{"curie": "MONDO:0022687", "names": ["Cerebellar atrophy", "Brain degeneration", "Cerebellum atrophy", "CEREBELLAR ATROPHY", "cerebellar atrophy", "Atrophic cerebellum", "cerebral degeneration", "Atrophy of cerebellum", "Infratentorial atrophy", "cerebellar degeneration", "Cerebellar degeneration", "Cerebellar Degeneration", "cerebellar Degeneration", "CEREBELLAR DEGENERATION", "degeneration; cerebellum", "cerebellum; degeneration", "Cerebellum--Degeneration", "Degeneration of cerebellum", "Cerebellar degeneration, NOS", "Atrophy of cerebellum (disorder)", "Cerebellar degeneration (disorder)", "cerebellum neurodegenerative disease", "neurodegenerative disease of cerebellum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellar degeneration", "shortest_name_length": 18}
{"curie": "UMLS:C1336463", "names": ["Stage I Lymphocyte Depleted Hodgkin Lymphoma", "Stage I Hodgkin's Lymphoma Lymphocyte Depleted", "Stage I Lymphocyte Depleted Hodgkin's Lymphoma", "Stage I Hodgkin's Disease Lymphocyte Depletion Type", "Stage I Hodgkin's Lymphoma Lymphocyte Depletion Type", "Stage I Lymphocyte-Depleted Classical Hodgkin Lymphoma", "Stage I Lymphocyte Depleted Classical Hodgkin Lymphoma", "Ann Arbor Stage I Lymphocyte-Depleted Classic Hodgkin Lymphoma", "Ann Arbor Stage I Lymphocyte-Depleted Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage I Lymphocyte-Depleted Classic Hodgkin Lymphoma", "shortest_name_length": 44}
{"curie": "MONDO:0002027", "names": ["Avoidant personality", "avoidant personality", "anxious personality disorder", "Anxious personality disorder", "Avoidant Personality Disorder", "avoidant personality disorder", "personality avoidant disorder", "avoidant disorder personality", "anxious; personality disorder", "Avoidant personality disorder", "personality disorder; anxious", "avoidant disorders personality", "avoidant; personality disorder", "Personality Disorder, Avoidant", "personality disorder; avoidant", "avoidant personality disorders", "Avoidant Personality Disorders", "Personality Disorders, Avoidant", "Anxious [avoidant] personality disorder", "Anxious personality disorder (disorder)", "anxious personality disorder (diagnosis)", "Avoidant personality disorder (disorder)", "avoidant personality disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "avoidant personality disorder", "shortest_name_length": 20}
{"curie": "UMLS:C4053934", "names": ["Tip Lesion Glomerulopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tip Lesion Glomerulopathy", "shortest_name_length": 25}
{"curie": "UMLS:C1334019", "names": ["High Grade PeIN", "High Grade Penile Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Penile Intraepithelial Neoplasia", "shortest_name_length": 15}
{"curie": "UMLS:C5420859", "names": ["Advanced Rhabdoid Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Rhabdoid Tumor", "shortest_name_length": 23}
{"curie": "MONDO:0005207", "names": ["Syncytioma", "chorioblastoma", "choriocarcinoma", "chordocarcinoma", "Choriocarcinoma", "CHORIOCARCINOMA", "Choriocarcinomas", "chordoepithelioma", "Chorioepithelioma", "chorion carcinoma", "chorioepithelioma", "Chorionepithelioma", "chorionepithelioma", "[M]Choriocarcinoma", "chorionic carcinoma", "choriocarcinoma NOS", "Choriocarcinoma NOS", "[M]Chorioepithelioma", "Choriocarcinoma, NOS", "Chorioepithelioma NOS", "chorionepithelioma NOS", "choriocarcinoma (disease)", "Choriocarcinoma (disorder)", "choriocarcinoma, malignant", "CHORIOCARCINOMA, MALIGNANT", "choriocarcinoma (diagnosis)", "Choriocarcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choriocarcinoma", "shortest_name_length": 10}
{"curie": "MONDO:0030815", "names": ["PFIC11", "cholestasis, progressive familial intrahepatic, 11", "CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholestasis, progressive familial intrahepatic, 11", "shortest_name_length": 6}
{"curie": "UMLS:C4526970", "names": ["Stage IIIA Gastric and Omental GIST AJCC v8", "Stage IIIA Gastric and Omental Gastrointestinal Stromal Tumor AJCC v8", "Stage IIIA Gastric (Stomach) and Omental Gastrointestinal Stromal Tumor (GIST)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Gastric and Omental Gastrointestinal Stromal Tumor AJCC v8", "shortest_name_length": 43}
{"curie": "UMLS:C5419751", "names": ["Refractory Acute Leukemia of Ambiguous Lineage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Acute Leukemia of Ambiguous Lineage", "shortest_name_length": 46}
{"curie": "MONDO:0007855", "names": ["Keratosis, Familial Actinic", "KERATOSIS, FAMILIAL ACTINIC", "keratosis, familial actinic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratosis, familial actinic", "shortest_name_length": 27}
{"curie": "MONDO:0000015", "names": ["Complement component deficiency", "complement component deficiency", "Complement component deficiency (disorder)", "complement component deficiency (diagnosis)", "classic complement early component deficiency", "genetic deficiency of early component of the classical complement pathway"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "classic complement early component deficiency", "shortest_name_length": 31}
{"curie": "MONDO:0005152", "names": ["Hypopituitalism", "Hypopituitarism", "HYPOPITUITARISM", "hypopituitarism", "HYPOPITUTITARISM", "Pituitary failure", "pituitary failure", "Hypopituitarism, NOS", "Pituitary deficiency", "pituitary hypofunction", "deficiencies pituitary", "Pituitary hypofunction", "INSUFFICIENCY PITUITARY", "Insufficiency pituitary", "insufficiency pituitary", "Pituitary Insufficiency", "pituitary insufficiency", "Pituitary insufficiency", "PITUITARY INSUFFICIENCY", "hypofunction; pituitary", "pituitary; hypofunction", "Insufficiency, Pituitary", "insufficiency; pituitary", "pituitary; insufficiency", "hypopituitarism; syndrome", "syndrome; hypopituitarism", "Hypopituitarism (disorder)", "Pituitary insufficiency NOS", "hypopituitarism (diagnosis)", "pituitary hormone deficiency", "Pituitary insufficiency, NOS", "Adenohypophyseal Hyposecretion", "Hyposecretion, Adenohypophyseal", "Anterior Pituitary Hyposecretion Syndrome", "Hyposecretion Syndrome, Anterior Pituitary", "Deficient secretion of one OR more pituitary hormones", "Deficient secretion of one or more pituitary hormones"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypopituitarism", "shortest_name_length": 15}
{"curie": "MONDO:0028226", "names": ["Autosomal Recessive SCN", "Autosomal Recessive Severe Congenital Neutropenia", "Autosomal recessive severe congenital neutropenia", "autosomal recessive severe congenital neutropenia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive severe congenital neutropenia", "shortest_name_length": 23}
{"curie": "UMLS:C4526615", "names": ["Stage IVB Thymoma", "Stage IVB Thymoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Thymoma AJCC v8", "shortest_name_length": 17}
{"curie": "UMLS:C4525090", "names": ["Stage III Colorectal Cancer AJCC v8", "Stage III Colorectal Carcinoma AJCC v8", "Stage III Colorectal (Colon or Rectal) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Colorectal Cancer AJCC v8", "shortest_name_length": 35}
{"curie": "MONDO:0043475", "names": ["Adams-Stokes", "Stokes-Adams", "Spens' syndrome", "Morgagni's disease", "adams attack stoke", "morgagni's disease", "adam attack stokes", "Adam Stokes attacks", "stokes-adams attack", "Stokes Adams attack", "STOKES ADAMS ATTACK", "Stokes-Adams attack", "Adam-Stokes attacks", "Adam-Stokes Attacks", "Adams Stokes attack", "adams stokes attack", "Adam Stokes Attacks", "adam-stokes syndrome", "Adams-Stokes; attack", "Stokes Adams Attacks", "Stokes-Adams; attack", "Attacks, Adam-Stokes", "attacks, Adam-Stokes", "adams stoke syndrome", "Stokes-Adams Attacks", "attack; Stokes-Adams", "stokes-adams attacks", "Adam-Stokes syndrome", "stoke adams syndrome", "Stokes-Adams attacks", "Stokes Adams attacks", "STOKES-ADAMS ATTACKS", "stokes adams attacks", "attack; Adams-Stokes", "STOKES ADAMS SYNDROME", "Stokes Adams Syndrome", "Morgagni-Stokes-Adams", "Adams Stokes syndrome", "SYNDROME STOKES-ADAMS", "Stokes-Adams syndrome", "Attacks, Stokes-Adams", "Stokes Adams syndrome", "stokes adams syndrome", "Stokes-Adams Syndrome", "Adams-Stokes Syndrome", "STOKES-ADAMS SYNDROME", "ADAMS-STOKES SYNDROME", "attacks, Stokes-Adams", "Syndrome Adams-Stokes", "Adams-Stokes syndrome", "adams stokes syndrome", "adams-stokes syndrome", "ADAMS STOKES SYNDROME", "SYNDROME ADAMS-STOKES", "stokes-adams syndrome", "Syndrome Stokes-Adams", "Adams Stokes Syndrome", "syndrome, Adams-Stokes", "syndrome, Stokes-Adams", "Syndrome, Stokes-Adams", "Syndrome, Adams-Stokes", "Stokes-Adams attack (disorder)", "Stokes-Adams-morgagni syndrome", "Stokes-Adams-Morgagni syndrome", "Morgagni-Adams-Stokes syndrome", "Morgagni-Adam's Stokes syndrome", "Stokes Adams syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adams-Stokes syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0020440", "names": ["persistent left SVC connecting to the left-sided atrium", "left superior caval vein persisting to the left-sided atrium", "persistent left superior vena cava connecting to the left-sided atrium", "persistent left superior caval vein connecting to the left-sided atrium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "persistent left superior vena cava connecting to the left-sided atrium", "shortest_name_length": 55}
{"curie": "UMLS:C3661489", "names": ["Autosomal Dominant Myotubular Myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Autosomal Dominant Myotubular Myopathy", "shortest_name_length": 38}
{"curie": "MONDO:0009848", "names": ["Scalp perifolliculitis", "Perifolliculitis of scalp", "cellulitis dissecting scalp", "Perifolliculitis of the scalp", "Dissecting cellulitis of scalp", "DISSECTING CELLULITIS OF THE SCALP", "dissecting cellulitis of the scalp", "Dissecting cellulitis of the scalp", "abscedens capitis perifolliculitis", "Dissecting Cellulitis of the Scalp", "Perifolliculitis capitis abscedens", "perifolliculitis; capitis abscedens", "capitis abscedens; perifolliculitis", "Folliculitis abscedens et suffodiens", "Dissecting perifolliculitis of scalp", "Folliculitis, abscedens et suffodiens", "folliculitis; abscedens et suffodiens", "Perifolliculitis capitis abscedens (disorder)", "Perifolliculitis capitis abscedens et suffodiens", "perifolliculitis capitis abscedens et suffodiens", "PERIFOLLICULITIS CAPITIS ABSCEDENS ET SUFFODIENS, FAMILIAL", "perifolliculitis capitis ABSCEDENS ET SUFFODIENS, familial", "Perifolliculitis Capitis Abscedens Et Suffodiens, Familial", "Perifolliculitis capitis abscedens et suffodiens (disorder)", "perifolliculitis capitis abscedens et suffodiens (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dissecting cellulitis of the scalp", "shortest_name_length": 22}
{"curie": "MONDO:0012414", "names": ["CLN10", "CLN10-NCL", "CLN10 disease", "Congenital NCL", "Cathepsin D deficiency", "Deficiency of cathepsin D", "CLN10 disease, adult (subtype)", "CLN10 disease, juvenile (subtype)", "neuronal ceroid lipofuscinosis 10", "Neuronal ceroid lipofuscinosis 10", "CLN10 disease, congenital (subtype)", "Ceroid Lipofuscinosis, Neuronal, 10", "CEROID LIPOFUSCINOSIS, NEURONAL, 10", "ceroid lipofuscinosis, neuronal, 10", "CTSD neuronal ceroid lipofuscinosis", "Deficiency of cathepsin D (disorder)", "neuronal ceroid lipofuscinosis type 10", "CLN10 disease, late infantile (subtype)", "ceroid lipofuscinosis, neuronal, type 10", "Congenital neuronal ceroid lipofuscinosis", "neuronal ceroid lipofuscinosis, congenital", "NEURONAL CEROID LIPOFUSCINOSIS, CONGENITAL", "Neuronal Ceroid Lipofuscinosis, Congenital", "ceroid lipofuscinosis neuronal Cathepsin D-deficient", "Cathepsin D deficient neuronal ceroid lipofuscinosis", "neuronal ceroid lipofuscinosis cathepsin D-deficient", "Ceroid Lipofuscinosis, Neuronal, Cathepsin D-Deficient", "CEROID LIPOFUSCINOSIS, NEURONAL, CATHEPSIN D-DEFICIENT", "ceroid lipofuscinosis, neuronal, Cathepsin D-deficient", "neuronal ceroid lipofuscinosis caused by mutation in CTSD", "Neuronal Ceroid Lipofuscinosis Due To Cathepsin D Deficiency", "neuronal ceroid lipofuscinosis due to Cathepsin D deficiency", "Neuronal ceroid lipofuscinosis due to cathepsin D deficiency", "NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCY", "neuronal ceroid lipofuscinosis due to cathepsin D deficiency", "Neuronal ceroid lipofuscinosis due to deficiency of cathepsin D", "Neuronal ceroid lipofuscinosis due to deficiency of cathepsin D (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuronal ceroid lipofuscinosis 10", "shortest_name_length": 5}
{"curie": "UMLS:C0341732", "names": ["bladder metaplasia squamous", "Squamous metaplasia of bladder", "squamous metaplasia of bladder", "Squamous Metaplasia of Bladder", "squamous cell; metaplasia, bladder", "squamous cell metaplasia of bladder", "Squamous metaplasia of bladder (disorder)", "squamous cell metaplasia of bladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Squamous metaplasia of bladder", "shortest_name_length": 27}
{"curie": "UMLS:C0239777", "names": ["Green Color Blindness", "GREEN COLOR BLINDNESS", "Color Blindness, Green"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Color Blindness, Green", "shortest_name_length": 21}
{"curie": "UMLS:C0588128", "names": ["implant infection", "Implant Infection", "Implant infection", "implant infections", "implants infections", "Infection and inflammatory reaction due to internal orthopedic fixation device", "infection and inflammatory reaction due to internal orthopedic fixation device", "Infection and inflammatory reaction due to internal orthopaedic fixation device", "Infection and inflammatory reaction due to internal orthopedic fixation device (disorder)", "infection and inflammatory reaction due to internal orthopedic fixation device (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infection and inflammatory reaction due to internal orthopedic fixation device", "shortest_name_length": 17}
{"curie": "UMLS:C0796661", "names": ["extracranial germ cell tumor", "Extracranial Germ Cell Tumor", "childhood extracranial germ cell tumor", "Childhood Extracranial Germ Cell Tumor", "pediatric extracranial germ cell tumor", "extracranial germ cell tumor, pediatric", "extracranial germ cell tumor, childhood", "germ cell tumor, extracranial, childhood", "germ cell tumor, childhood, extracranial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Extracranial Germ Cell Tumor", "shortest_name_length": 28}
{"curie": "UMLS:C4687536", "names": ["Mediastinal Granulocytic Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mediastinal Granulocytic Sarcoma", "shortest_name_length": 32}
{"curie": "MONDO:0009403", "names": ["hypertelorism and tetralogy of fallot", "HYPERTELORISM AND TETRALOGY OF FALLOT", "Hypertelorism and tetralogy of Fallot"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertelorism and tetralogy of fallot", "shortest_name_length": 37}
{"curie": "UMLS:C5203838", "names": ["Bladder Soft Tissue Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder Soft Tissue Neoplasm", "shortest_name_length": 28}
{"curie": "MONDO:0032928", "names": ["TLIND", "T-CELL LYMPHOPENIA, INFANTILE, WITH OR WITHOUT NAIL DYSTROPHY, AUTOSOMAL DOMINANT", "T-cell lymphopenia, infantile, with or without nail dystrophy, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-cell lymphopenia, infantile, with or without nail dystrophy, autosomal dominant", "shortest_name_length": 5}
{"curie": "MONDO:0010992", "names": ["AYGRP", "Aymé-Gripp syndrome", "AYME-GRIPP SYNDROME", "AYME-Gripp syndrome", "Ayme-Gripp syndrome", "cataracts, congenital, with sensorineural deafness, Down syndrome-like Facial appearance, short stature, and mental retardation", "cataracts, congenital, with sensorineural deafness, Down syndrome-like facial appearance, short stature, and mental retardation", "Cataracts, Congenital, with Sensorineural Deafness, Down Syndrome-Like Facial Appearance, Short Stature, and Mental Retardation", "CATARACTS, CONGENITAL, WITH SENSORINEURAL DEAFNESS, DOWN SYNDROME-LIKE FACIAL APPEARANCE, SHORT STATURE, AND MENTAL RETARDATION", "cataracts, congenital, with sensorineural deafness, Down syndrome-like Facial appearance, short stature, and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ayme-Gripp syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0044339", "names": ["IDD", "Spinal discopathy", "discogenic disease", "DISCOGENIC DISEASE", "lumbar disc disease", "discogenic; disorder", "VERTEBRA DISC DISEASE", "VERTEBRAL DISC DISEASE", "lumbar Disc Degeneration", "Lumbar Disc Degeneration", "lumbar disc degeneration", "Lumbar disc degeneration", "degenerative disc disease", "degenerative disc disorder", "intervertebral disk disease", "Intervertebral disc disease", "degeneration of lumbar disc", "intervertebral disc disease", "INTERVERTEBRAL DISK DISEASE", "INTERVERTEBRAL DISC DISEASE", "disease (or disorder); disc", "intervertebral DISC disease", "intervertebral disk syndrome", "Intervertebral disk syndrome", "Intervertebral disc disorder", "intervertebral disc disorder", "intervertebral disc disorders", "Intervertebral disc disorders", "Disorder of intervertebral disc", "Intervertebral disc disorder NOS", "lumbar Disc degenerative disease", "Lumbar Disc Degenerative Disease", "Intervertebral disc disorder, NOS", "disease (or disorder); discogenic", "lumbar disc degenerative disorder", "Lumbar Disc Degenerative Disorder", "lumbar Disc degenerative disorder", "lumbar disc disease, susceptibility to", "Intervertebral disc disorder (disorder)", "intervertebral disc disorder (diagnosis)", "Intervertebral disc disorder, unspecified", "lumbar disc herniation, susceptibility to", "degeneration; intervertebral disc, lumbar", "degeneration of lumbar intervertebral disc", "Degeneration of lumbar intervertebral disc", "disease (or disorder); intervertebral disc", "lumbar disc degeneration, susceptibility to", "intervertebral disc disease, susceptibility to", "Degeneration of lumbar intervertebral disc (disorder)", "degeneration of lumbar intervertebral disc (diagnosis)", "lumbar region of vertebral column intervertebral disc degenerative disorder", "intervertebral disc degenerative disorder of lumbar region of vertebral column"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lumbar disc degenerative disorder", "shortest_name_length": 3}
{"curie": "MONDO:0700099", "names": ["adenocarcinoma, non-human animal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenocarcinoma, non-human animal", "shortest_name_length": 32}
{"curie": "MONDO:0010373", "names": ["POF2B", "Premature Ovarian Failure 2b", "premature ovarian failure 2B", "PREMATURE OVARIAN FAILURE 2B", "POF1B primary ovarian failure", "primary ovarian insufficiency 2B", "premature ovarian failure type 2B", "premature ovarian failure 2B, X-linked recessive", "primary ovarian failure caused by mutation in POF1B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "premature ovarian failure 2B", "shortest_name_length": 5}
{"curie": "UMLS:C0002879", "names": ["ANEMIA HEMOLYTIC ACQUIRED", "Acquired hemolytic anemia", "Hemolytic anemia acquired", "acquired hemolytic anemia", "Acquired Hemolytic Anemia", "acquired anemia hemolytic", "Hemolytic Anemia, Acquired", "Anemia, Acquired Hemolytic", "Acquired hemolytic anemias", "Acquired Hemolytic Anemias", "acquired haemolytic anaemia", "Anemia, Hemolytic, Acquired", "Haemolytic anaemia acquired", "Anaemia;haemolytic;acquired", "Acquired haemolytic anaemia", "anemia; hemolytic, acquired", "hemolytic; anemia, acquired", "Acquired hemolytic anemia NOS", "Acquired hemolytic anemia, NOS", "Acquired haemolytic anaemia, NOS", "Acquired hemolytic anemia (disorder)", "acquired hemolytic anemia (diagnosis)", "Acquired hemolytic anemia, unspecified", "Acquired haemolytic anaemia, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anemia, Hemolytic, Acquired", "shortest_name_length": 25}
{"curie": "MONDO:0020392", "names": ["discrete fixed membranous subaortic stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "discrete fixed membranous subaortic stenosis", "shortest_name_length": 44}
{"curie": "UMLS:C1332939", "names": ["Childhood Acute Lymphoid Leukemia in Complete Remission", "Pediatric Acute Lymphoid Leukemia in Complete Remission", "Acute Lymphoblastic Leukemia (ALL) in Complete Remission", "Pediatric Acute Lymphocytic Leukemia in Complete Remission", "Childhood Acute Lymphocytic Leukemia in Complete Remission", "Pediatric Acute Lymphogenous Leukemia in Complete Remission", "Childhood Acute Lymphogenous Leukemia in Complete Remission", "Pediatric Acute Lymphoblastic Leukemia in Complete Remission", "Childhood Acute Lymphoblastic Leukemia in Complete Remission", "Childhood Precursor Lymphoblastic Leukemia in Complete Remission"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Acute Lymphoblastic Leukemia in Complete Remission", "shortest_name_length": 55}
{"curie": "MONDO:0014965", "names": ["LCCS11", "lethal congenital contracture syndrome 11", "LETHAL CONGENITAL CONTRACTURE SYNDROME 11", "GLDN lethal congenital contracture syndrome", "lethal congenital contracture syndrome type 11", "lethal congenital contracture arthrogryposis-11", "lethal congenital contracture syndrome 11; LCCS11", "lethal congenital contracture syndrome caused by mutation in GLDN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal congenital contracture syndrome 11", "shortest_name_length": 6}
{"curie": "MONDO:0014509", "names": ["VMD5", "vitelliform macular dystrophy 5", "MACULAR DYSTROPHY, VITELLIFORM, 5", "macular dystrophy, vitelliform, 5", "IMPG2 vitelliform macular dystrophy", "macular dystrophy, vitelliform, type 5", "vitelliform macular dystrophy caused by mutation in IMPG2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitelliform macular dystrophy 5", "shortest_name_length": 4}
{"curie": "MONDO:0016688", "names": ["Fibrous astrocytoma", "Fibrillary Astrocytoma", "Fibrillary astrocytoma", "fibrillary astrocytoma", "Astrocytoma, Fibrillary", "Fibrillary Astrocytomas", "Fibrillary Astrocytic tumors", "fibrillary astrocytic tumors", "astrocytoma; fibrous, unspecified site", "fibrous; astrocytoma, unspecified site", "astrocytoma; fibrillary, unspecified site", "fibrillary; astrocytoma, unspecified site", "Fibrillary astrocytoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibrillary astrocytoma", "shortest_name_length": 19}
{"curie": "UMLS:C4744522", "names": ["Third Ventricle Pilocytic Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Third Ventricle Pilocytic Astrocytoma", "shortest_name_length": 37}
{"curie": "UMLS:C3899382", "names": ["Dialyzer Reaction", "Dialysis Membrane Reaction", "Dialysis membrane reaction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dialysis membrane reaction", "shortest_name_length": 17}
{"curie": "MONDO:0005183", "names": ["ovary cystadenoma", "simple cystadenoma", "Ovarian cystadenoma", "ovarian cystadenoma", "Ovarian Cystadenoma", "cystadenoma of ovary", "Cystadenoma of Ovary", "simple ovarian cystoma", "Simple Ovarian Cystoma", "cystoma serosum simplex", "Cystoma Serosum Simplex", "Simple cystoma of ovary", "simple cystoma of ovary", "Cystoma Serosum simplex", "Simple Cystoma of Ovary", "Cystadenoma of the Ovary", "cystadenoma of the ovary", "benign ovarian cystadenoma", "Benign Ovarian Cystadenoma", "benign cystadenoma of ovary", "Simple cystoma of the ovary", "Benign Cystadenoma of Ovary", "Simple Cystoma of the Ovary", "simple cystoma of the ovary", "Benign Cystadenoma of the Ovary", "benign cystadenoma of the ovary", "Simple cystoma of the ovary (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian cystadenoma", "shortest_name_length": 17}
{"curie": "UMLS:C5556898", "names": ["Urinary System Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urinary System Carcinoma", "shortest_name_length": 24}
{"curie": "MONDO:0009557", "names": ["MAD", "MADA", "mandibuloacral dysplasia", "Mandibuloacral dysplasia", "Mandibuloacral dysostosis", "Familial mandibuloacral dysplasia", "Craniomandibular dermatodysostosis", "craniomandibular Dermatodysostosis", "Craniomandibular Dermatodysostosis", "CRANIOMANDIBULAR DERMATODYSOSTOSIS", "Mandibuloacral dysostosis (disorder)", "mandibuloacral dysplasia type A lipodystrophy", "MANDIBULOACRAL dysplasia with type A lipodystrophy", "Mandibuloacral Dysplasia with Type A Lipodystrophy", "MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY", "mandibuloacral dysplasia with type A lipodystrophy", "Mandibuloacral dysplasia with type A lipodystrophy", "MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL", "Mandibuloacral dysplasia with type a lipodystrophy, atypical", "Mandibuloacral Dysplasia with Type A Lipodystrophy, Atypical", "LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA", "lipodystrophy, type A, associated with Mandibuloacral dysplasia", "Lipodystrophy, type A, associated with mandibuloacral dysplasia", "Mandibuloacral dysostosis co-occurrent with type A lipodystrophy", "Mandibuloacral dysostosis co-occurrent with type A lipodystrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mandibuloacral dysplasia with type A lipodystrophy", "shortest_name_length": 3}
{"curie": "MONDO:0007811", "names": ["ICE SYNDROME", "Ice syndrome", "Ichthyosis cheek eyebrow syndrome", "ichthyosis cheek eyebrow syndrome", "Ichthyosis-Cheek-Eyebrow Syndrome", "ichthyosis-cheek-eyebrow syndrome", "ICHTHYOSIS--CHEEK--EYEBROW SYNDROME", "ichthyosis--cheek--eyebrow syndrome", "Sidransky Feinstein Goodman syndrome", "Sidransky-Feinstein-Goodman syndrome", "ICE (ichthyosis cheek eyebrow) syndrome", "Ichthyosis cheek eyebrow syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ichthyosis-cheek-eyebrow syndrome", "shortest_name_length": 12}
{"curie": "EFO:1001495", "names": ["small artery occlusion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small artery occlusion", "shortest_name_length": 22}
{"curie": "UMLS:C3647834", "names": ["Grade 3a", "Grade 3a Follicular Lymphoma", "Follicular Lymphoma Grade 3a", "Follicular lymphoma grade 3a", "grade 3A follicular lymphoma", "Follicular lymphoma, grade 3A", "Follicular lymphoma grade IIIa", "Follicular lymphoma grade 3a (disorder)", "grade 3A follicular lymphoma (diagnosis)", "Follicular non-Hodgkin lymphoma grade 3a", "WHO Follicular Lymphoma Histologic Grade 3a", "Follicular lymphoma grade 3a (morphologic abnormality)", "malignant neoplasm nodular lymphoma follicular grade 3a"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "grade 3A follicular lymphoma", "shortest_name_length": 8}
{"curie": "MONDO:0016237", "names": ["Multiple progressive angiomata", "diffuse neonatal hemangiomatosis", "Diffuse neonatal hemangiomatosis", "Diffuse neonatal haemangiomatosis", "Eruptive neonatal hemangiomatosis", "Multiple progressive hemangiomata", "Eruptive neonatal haemangiomatosis", "Multiple progressive haemangiomata", "Multiple progressive hemangiomata (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diffuse neonatal hemangiomatosis", "shortest_name_length": 30}
{"curie": "UMLS:C4528615", "names": ["Vulvar Cancer by AJCC v8 Stage", "Vulvar Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Cancer by AJCC v8 Stage", "shortest_name_length": 30}
{"curie": "UMLS:C4553571", "names": ["Stage III Primary Peritoneal Cancer", "Stage III Primary Peritoneal Cancer AJCC v8", "Stage III Primary Peritoneal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Primary Peritoneal Cancer AJCC v8", "shortest_name_length": 35}
{"curie": "MONDO:0004864", "names": ["acute allergic mucoid otitis media", "Acute allergic mucoid otitis media", "Acute allergic mucoid otitis media (disorder)", "acute allergic mucoid otitis media (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute allergic mucoid otitis media", "shortest_name_length": 34}
{"curie": "MONDO:0700162", "names": ["canine granular cell tumor", "Canine Granular Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canine granular cell tumor", "shortest_name_length": 26}
{"curie": "UMLS:C0741276", "names": ["Atriomegaly", "ATRIAL ENLARGEMENT", "atrial enlargement", "Atrial enlargement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ATRIAL ENLARGEMENT", "shortest_name_length": 11}
{"curie": "UMLS:C3274518", "names": ["Surfactant Protein Deficiency", "Surfactant Apoprotein Abnormality"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Surfactant Protein Deficiency", "shortest_name_length": 29}
{"curie": "MONDO:0008495", "names": ["dense body defect", "Dense body defect", "Dense body deficiency", "Storage Pool Deficiency", "Storage pool deficiency", "Deficiency, Storage Pool", "Storage Pool Deficiencies", "Deficiencies, Storage Pool", "Delta storage pool disease", "Dense body defect (disorder)", "platelet storage pool defect", "Platelet storage pool defect", "storage pool platelet disease", "Platelet Storage Pool Disease", "STORAGE POOL PLATELET DISEASE", "Storage Pool Platelet Disease", "alpha delta granule deficiency", "platelet storage pool diseases", "alpha dense granule deficiency", "platelet storage pool deficiency", "Platelet storage pool deficiency", "Nucleotide storage pool disorder", "Platelet Storage Pool Deficiency", "platelet dense granule deficiency", "Deficiency, Platelet Storage Pool", "Platelet storage organelle defect", "Platelet dense granule deficiency", "Storage pool disease of platelets", "Storage Pool Deficiency, Platelet", "Platelet Storage Pool Deficiencies", "Dense granule deficiency in platelets", "Platelet storage pool defect (disorder)", "Platelet dense granule deficiency (disorder)", "combined alpha-delta platelet storage pool deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "platelet storage pool deficiency", "shortest_name_length": 17}
{"curie": "UMLS:C1516552", "names": ["Overt Primary Myelofibrosis", "Primary Myelofibrosis, Fibrotic Stage", "Primary Myelofibrosis, Overt Fibrotic Stage", "Chronic Idiopathic Myelofibrosis, Fibrotic Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Overt Primary Myelofibrosis", "shortest_name_length": 27}
{"curie": "MONDO:0014944", "names": ["SBIDDS", "short stature-brachydactyly-obesity-global developmental delay syndrome", "SHORT STATURE, BRACHYDACTYLY, IMPAIRED INTELLECTUAL DEVELOPMENT, AND SEIZURES", "short stature, brachydactyly, intellectual developmental disability, and seizures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short stature-brachydactyly-obesity-global developmental delay syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0030014", "names": ["LGMDR26", "muscular dystrophy, limb-girdle, autosomal recessive 26", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 26"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy, limb-girdle, autosomal recessive 26", "shortest_name_length": 7}
{"curie": "MONDO:0005015", "names": ["dm", "DM", "diabetes", "Diabetes", "diabetes NOS", "Diabetes NOS", "diabetes (DM)", "diabete mellitus", "Diabetes mellitus", "diabetes mellitus", "Diabetes_Mellitus", "DIABETES MELLITUS", "Diabetes Mellitus", "Diabetes mellitus NOS", "DIABETES MELLITUS NOS", "DM - Diabetes mellitus", "diabetes mellitus (DM)", "Diabetes mellitus, NOS", "Diabetes mellitus (DM)", "disorder diabetes mellitus", "diabetes mellitus (disease)", "Diabetes mellitus (E08-E13)", "Diabetes mellitus (disorder)", "diabetes mellitus (diagnosis)", "Unspecified diabetes mellitus", "DIABETES MELLITUS NOS DIAGNOSED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diabetes mellitus", "shortest_name_length": 2}
{"curie": "UMLS:C4682894", "names": ["Renal Pelvis Cancer by AJCC v7 Stage", "Renal Pelvis Urothelial Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal Pelvis Cancer by AJCC v7 Stage", "shortest_name_length": 36}
{"curie": "MONDO:0011206", "names": ["ventriculomegaly with defects of the radius and kidney", "VENTRICULOMEGALY WITH DEFECTS OF THE RADIUS AND KIDNEY", "Ventriculomegaly With Defects Of The Radius And Kidney"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ventriculomegaly with defects of the radius and kidney", "shortest_name_length": 54}
{"curie": "MONDO:0011069", "names": ["Frydman Cohen Ashkenazi syndrome", "Cervical ribs sprengel anomaly anal atresia urethral obstruction", "Cervical Ribs, Sprengel Anomaly, Anal Atresia, and Urethral Obstruction", "CERVICAL RIBS, SPRENGEL ANOMALY, ANAL ATRESIA, AND URETHRAL OBSTRUCTION", "cervical ribs, Sprengel anomaly, anal atresia, and urethral obstruction", "cervical ribs, Sprengel anomaly, preaxial polydactyly, anal atresia, and urethral obstruction", "Cervical ribs, Sprengel anomaly, preaxial polydactyly, anal atresia, and urethral obstruction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical ribs, Sprengel anomaly, anal atresia, and urethral obstruction", "shortest_name_length": 32}
{"curie": "UMLS:C0342174", "names": ["abscess; thyroid", "thyroid; abscess", "Abscess of thyroid", "Thyroid gland abscess", "Thyroid Gland Abscess", "Abscess of thyroid (disorder)", "Abscess of thyroid (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abscess of thyroid", "shortest_name_length": 16}
{"curie": "MONDO:0005508", "names": ["EXT", "HMO", "EXT1", "Familial Exostoses", "Familial Exostosis", "multiple exostoses", "DIAPHYSEAL ACLASIS", "multiple exostosis", "Multiple Exostoses", "Diaphyseal aclasis", "Multiple Exostosis", "diaphyseal aclasis", "Diaphyseal aclasia", "Multiple exostoses", "diaphysial aclasis", "Diaphyseal Aclases", "Diaphyseal Aclasis", "diaphyseal aclases", "exostoses, multiple", "EXOSTOSIS, MULTIPLE", "Exostoses, Multiple", "Aclases, Diaphyseal", "Aclasis, Diaphyseal", "multiple; exostosis", "Exostosis, Multiple", "Exostosis, Familial", "ACLASIS, DIAPHYSEAL", "Exostoses, Familial", "Osteochondromatosis", "aclasis; diaphyseal", "exostosis; multiple", "OSTEOCHONDROMATOSIS", "Bessel-Hagen disease", "Bessel Hagen disease", "Bessel-Hagen Disease", "Multiple Osteochondroma", "multiple osteochondroma", "Multiple osteochondroma", "multiple ostechondromas", "Multiple Osteochondromas", "MULTIPLE OSTEOCHONDROMAS", "multiple osteochondromas", "Osteochondroma, Multiple", "Osteochondromas, Multiple", "multiple exostosis type I", "Multiple exostoses type I", "Multiple exostoses syndrome", "Exostoses, Multiple, Type I", "EXOSTOSES, MULTIPLE, TYPE I", "Multiple exostosis syndrome", "multiple exostosis syndrome", "OSTEOCHONDROMATOSIS, OLLIER", "Multiple Osteochondromatosis", "multiple exostosis syndromes", "multiple osteochondromatosis", "multiple congenital exotoses", "Multiple osteochondromatosis", "Osteochondromatosis syndrome", "osteochondromatosis syndrome", "Multiple exostosis syndromes", "hereditary multiple exostosis", "Hereditary Multiple Exostosis", "syndrome; osteochondromatosis", "hereditary exostosis multiple", "multiple hereditary exostoses", "hereditary multiple exostoses", "multiple hereditary exostosis", "osteochondromatosis; syndrome", "Multiple Hereditary Exostoses", "Multiple congenital exostosis", "multiple congenital exostosis", "Hereditary Multiple Exostoses", "Multiple hereditary exostosis", "Hereditary multiple exostosis", "OSTEOCHONDROMATOSIS, MULTIPLE", "Multiple congenital exostoses", "Exostoses, Multiple Hereditary", "Exostosis, Hereditary Multiple", "exostosis, hereditary multiple", "Exostoses, Hereditary Multiple", "Multiple Exostoses, Hereditary", "multiple exostosis (diagnosis)", "Hereditary Exostoses, Multiple", "Multiple Exostosis, Hereditary", "hereditary multiple exostoses 2", "hereditary multiple exostoses 3", "hereditary multiple exostoses 1", "Multiple cartilaginous exostoses", "multiple cartilaginous exostosis", "Multiple Cartilaginous Exostosis", "multiple cartilaginous exostoses", "Multiple cartilaginous exostosis", "Multiple Cartilaginous Exostoses", "MULTIPLE CARTILAGINOUS EXOSTOSES", "Exostosis, Multiple Cartilaginous", "Cartilaginous Exostosis, Multiple", "Exostoses, Multiple Cartilaginous", "Cartilaginous Exostoses, Multiple", "hereditary multiple osteochondromas", "Multiple osteochondroma of long bone", "Hereditary deforming chondrodysplasia", "Hereditary Deforming Chondrodysplasia", "multiple exostosis type I (diagnosis)", "DYSCHONDROPLASIA, HEREDITARY DEFORMING", "Deforming Chondrodysplasia, Hereditary", "Hereditary Deforming Chondrodysplasias", "Chondrodysplasia, Hereditary Deforming", "CHONDRODYSPLASIA, HEREDITARY DEFORMING", "Chondrodysplasias, Hereditary Deforming", "Deforming Chondrodysplasias, Hereditary", "Multiple congenital exostosis (disorder)", "multiple congenital exotoses (diagnosis)", "Multiple osteochondroma of long bone (disorder)", "osteochondromatosis syndrome (disorder) [ambiguous]", "Diaphyseal aclasis-external chondromatosis syndrome", "Diaphyseal aclasis, external chondromatosis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary multiple osteochondromas", "shortest_name_length": 3}
{"curie": "MONDO:0015637", "names": ["benign non-familial infantile seizures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign non-familial infantile seizures", "shortest_name_length": 38}
{"curie": "UMLS:C0853013", "names": ["Diverticular perforation", "Diverticular perforation NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diverticular perforation", "shortest_name_length": 24}
{"curie": "UMLS:C2713546", "names": ["AR Deficiency", "Deficiency, AR", "DHTR Deficiency", "AR Deficiencies", "Deficiency, DHTR", "Deficiencies, AR", "DHTR Deficiencies", "Deficiencies, DHTR", "Androgen Receptor Deficiency", "Receptor Deficiency, Androgen", "Deficiency, Androgen Receptor", "Androgen Receptor Deficiencies", "Receptor Deficiencies, Androgen", "Deficiencies, Androgen Receptor", "Dihydrotestosterone Receptor Deficiency", "Receptor Deficiency, Dihydrotestosterone", "Deficiency, Dihydrotestosterone Receptor", "Dihydrotestosterone Receptor Deficiencies", "Deficiencies, Dihydrotestosterone Receptor", "Receptor Deficiencies, Dihydrotestosterone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Androgen Receptor Deficiency", "shortest_name_length": 13}
{"curie": "UMLS:C4082928", "names": ["mesenteric thrombosis", "Thrombosis:mesenteric", "Mesenteric Thrombosis", "Mesenteric thrombosis", "mesenteric; thrombosis", "thrombosis; mesenteric"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mesenteric thrombosis", "shortest_name_length": 21}
{"curie": "UMLS:C1335027", "names": ["Non-Neoplastic Paranasal Sinus Disease", "Non-Neoplastic Paranasal Sinus Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Paranasal Sinus Disorder", "shortest_name_length": 38}
{"curie": "UMLS:C4726599", "names": ["Unresectable Rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Rhabdomyosarcoma", "shortest_name_length": 29}
{"curie": "UMLS:C4521751", "names": ["Stage 0 Gastric (Stomach) Cancer", "Clinical Stage 0 Gastric Cancer AJCC v8", "Clinical Stage 0 Gastric Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage 0 Gastric Cancer AJCC v8", "shortest_name_length": 32}
{"curie": "UMLS:C4727372", "names": ["Recurrent Lobular Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Lobular Breast Carcinoma", "shortest_name_length": 34}
{"curie": "UMLS:C4329630", "names": ["Central Nervous System Epithelioid Hemangioendothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Epithelioid Hemangioendothelioma", "shortest_name_length": 55}
{"curie": "MONDO:0004620", "names": ["LDHL", "LDCHL", "adult LDHD", "Adult HDLD", "adult HDLD", "Adult LDHD", "HDLD, adult", "LDHD, adult", "HD LD, adult", "LD HD, adult", "lymphocyte depleted HD, adult", "Hodgkin; lymphocytic depletion", "lymphocyte depletion HD, adult", "HD, lymphocyte depleted, adult", "Lymphocyte depleted Hodgkin lymphoma", "Lymphocyte Depleted Hodgkin Lymphoma", "Hodgkin Lymphoma Lymphocyte Depleted", "lymphocyte depleted Hodgkin lymphoma", "Hodgkin lymphoma, lymphocyte depleted", "Lymphocyte-Depleted Hodgkin's Disease", "Lymphocyte Depleted Hodgkin's Disease", "Hodgkin lymphoma, lymphocyte depletion", "Hodgkin's Disease Lymphocyte Depletion", "Lymphocyte-Depleted Hodgkin's Lymphoma", "Hodgkin disease, lymphocytic depletion", "Hodgkin's Lymphoma Lymphocyte Depleted", "Lymphocyte Depleted Hodgkin's Lymphoma", "Lymphocyte Depletion Hodgkin's Lymphoma", "Hodgkin's disease, lymphocytic depletion", "disease; Hodgkin's, lymphocytic depletion", "Hodgkin's lymphoma, lymphocytic depletion", "adult lymphocyte depleted Hodgkin lymphoma", "Adult Lymphocyte Depleted Hodgkin Lymphoma", "adult lymphocyte depletion Hodgkin lymphoma", "Hodgkin Lymphoma, Lymphocyte Depletion, NOS", "Hodgkin's disease with lymphocytic depletion", "Adult Lymphocyte Depletion Hodgkin's Disease", "lymphocyte depleted Hodgkin's disease, adult", "Hodgkin's disease, lymphocytic depletion NOS", "Adult Lymphocyte Depleted Hodgkin's Lymphoma", "adult lymphocyte depleted Hodgkin's lymphoma", "adult lymphocyte depletion Hodgkin's disease", "Lymphocyte-Depleted Classic Hodgkin Lymphoma", "adult Hodgkin's disease, lymphocyte depleted", "lymphoma, lymphocyte depleted adult Hodgkin's", "Hodgkin's disease, lymphocytic depletion, NOS", "Hodgkin's disease, lymphocyte depleted, adult", "Lymphocyte-Depleted Classical Hodgkin Lymphoma", "Lymphocyte depleted classical Hodgkin lymphoma", "Hodgkin's lymphoma, lymphocyte depleted, adult", "Lymphocyte Depleted Classical Hodgkin Lymphoma", "lymphocyte-depleted classical Hodgkin lymphoma", "Classical Hodgkin lymphoma, lymphocyte depletion", "lymphocyte depleted Hodgkin lymphoma (diagnosis)", "Lymphocyte Depleted Classical Hodgkin's Lymphoma", "Hodgkin lymphoma, lymphocyte depletion, reticular", "Classic Hodgkin lymphoma, lymphocyte-depleted type", "Adult lymphocyte-depleted Classic Hodgkin lymphoma", "classic Hodgkin lymphoma, lymphocyte-depleted type", "Adult Lymphocyte-Depleted Classic Hodgkin Lymphoma", "Hodgkin's lymphocytic depletion of unspecified site", "Hodgkin's disease, lymphocytic depletion (clinical)", "Hodgkin's disease, lymphocytic depletion (disorder)", "Adult Lymphocyte-Depleted Classical Hodgkin Lymphoma", "adult lymphocyte depleted classical Hodgkin lymphoma", "adult lymphocyte-depleted classical Hodgkin lymphoma", "Adult Lymphocyte Depleted Classical Hodgkin Lymphoma", "Hodgkin lymphoma, lymphocyte depletion, diffuse fibrosis", "Hodgkin's disease lymphocyte depletion type stage unspecified", "Hodgkin lymphoma, lymphocyte depletion (morphologic abnormality)", "Classical Hodgkin lymphoma, lymphocyte depletion, diffuse fibrosis", "Hodgkin's disease, lymphocytic depletion NOS (morphologic abnormality)", "Hodgkin's disease, lymphocytic depletion, unspecified site, extranodal and solid organ sites"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's lymphoma, lymphocytic depletion", "shortest_name_length": 4}
{"curie": "MONDO:0006920", "names": ["Prediabetes", "prediabetes", "Pre diabetes", "pre diabetic", "pre-diabetic", "pre diabetes", "Pre-diabetic", "pre-diabetes", "Pre-diabetes", "pre diabetics", "Pre-diabetes NOS", "prediabetic state", "Prediabetic State", "Prediabetic state", "State, Prediabetic", "Prediabetic States", "borderline diabetes", "Borderline diabetes", "diabetes borderline", "States, Prediabetic", "Borderline Diabetes", "prediabetes syndrome", "Prediabetes syndrome", "Prediabetes (finding)", "impaired glucose tolerance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prediabetes syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0100397", "names": ["AML, t(9;22)(q34;q11)", "AML, t(9;22)(q34;q11.2)", "AML, t(9;22)(q34.1;q11.2)", "acute myeloid leukemia, t(9;22)(q34.1;q11.2)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, t(9;22)(q34.1;q11.2)", "shortest_name_length": 21}
{"curie": "MONDO:0006859", "names": ["adenoma mucinous", "Mucinous adenoma", "Mucinous Cystoma", "Mucinous cystoma", "Mucinous Adenoma", "mucinous cystoma", "mucinous adenoma", "Mucinous Cystadenoma", "Mucinous cystadenoma", "CYSTADENOMA MUCINOUS", "mucinous cystadenoma", "cystadenoma mucinous", "Mucinous Cystadenomas", "Cystadenoma, Mucinous", "mucinous cystadenomas", "Cystadenomas, Mucinous", "Mucinous cystadenoma NOS", "ADENOMA, MUCINOUS, BENIGN", "adenoma, mucinous, benign", "Mucinous cystadenoma, NOS", "pseudomucinous cystadenoma", "Pseudomucinous Cystadenoma", "Pseudomucinous cystadenoma", "[M]Mucinous cystadenoma NOS", "Pseudomucinous cystadenoma, NOS", "cystoma; mucinous, unspecified site", "mucinous; cystoma, unspecified site", "mucinous; cystadenoma, unspecified site", "cystadenoma; mucinous, unspecified site", "Mucinous adenoma (morphologic abnormality)", "pseudomucinous; cystadenoma, unspecified site", "cystadenoma; pseudomucinous, unspecified site", "Mucinous cystadenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucinous cystadenoma", "shortest_name_length": 16}
{"curie": "MONDO:0009234", "names": ["HMWK", "FLAUJEAC TRAIT", "Williams trait", "WILLIAMS TRAIT", "Flaujeac trait", "HMWK deficiency", "HMWK DEFICIENCY", "HMWK Deficiency", "FITZGERALD TRAIT", "Fitzgerald trait", "Fitzgerald Trait", "Kininogen deficiency", "kininogen deficiency", "Flaujeac trait, included", "Williams trait, included", "Williams factor deficiency", "Flaujeac factor deficiency", "Reduced kininogen activity", "kininogen deficiency, total", "KININOGEN DEFICIENCY, TOTAL", "Kininogen Deficiency, Total", "Fitzgerald factor deficiency", "Fitzgerald-Flaujeac-Williams-Reid trait", "high molecular weight kininogen deficiency", "High molecular weight kininogen deficiency", "High Molecular Weight Kininogen Deficiency", "HIGH MOLECULAR WEIGHT KININOGEN DEFICIENCY", "Kininogen Deficiency, High Molecular Weight", "KININOGEN DEFICIENCY, HIGH MOLECULAR WEIGHT", "kininogen deficiency, high molecular weight", "Williams-Fitzgerald-Flaujeac factor deficiency", "congenital high-molecular-weight kininogen deficiency", "High molecular weight kininogen deficiency (disorder)", "Fitzgerald trait kininogen deficiency, total, included", "high-molecular-weight kininogen deficiency, congenital", "kininogen deficiency, high molecular weight and Low molecular weight", "Kininogen Deficiency, High Molecular Weight and Low Molecular Weight", "KININOGEN DEFICIENCY, HIGH MOLECULAR WEIGHT AND LOW MOLECULAR WEIGHT", "kininogen deficiency, high molecular weight and LOW molecular weight, included"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital high-molecular-weight kininogen deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0015752", "names": ["intellectual disability-cataracts-kyphosis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability-cataracts-kyphosis syndrome", "shortest_name_length": 51}
{"curie": "MONDO:0001663", "names": ["macula cyst", "macula; cyst", "cyst; macula", "Macular cyst", "macular cyst", "hole retinal cyst", "Hole retinal cyst", "Macular retinal cyst", "Macular cyst or hole", "macular cyst or hole", "macular cyst (diagnosis)", "macular cyst(s) were observed", "macular pseudohole retinal cyst", "Macular pseudohole retinal cyst", "Macular retinal cyst (disorder)", "macular cyst (physical finding)", "Macular cyst, hole, or pseudohole", "Macular cyst, hole, or pseudohole of retina", "macular cyst, hole, or pseudohole of retina", "Degeneration of macula due to cyst, hole or pseudohole", "macular degeneration, due to cyst, hole, or pseudohole", "Degeneration of macula due to cyst, hole or pseudohole (disorder)", "macular degeneration, due to cyst, hole, or pseudohole (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hole retinal cyst", "shortest_name_length": 11}
{"curie": "UMLS:C0334313", "names": ["Mixed Acidophil-Basophil Carcinoma", "Mixed acidophil-basophil carcinoma", "Mixed Eosinophil-Basophil Carcinoma", "Mixed Acidophil-Basophil Adenocarcinoma", "carcinoma; acidophil-basophil, unspecified site", "basophil-acidophil; carcinoma, unspecified site", "acidophil-basophil; carcinoma, unspecified site", "Pituitary Gland Mixed Acidophil-Basophil Carcinoma", "mixed acidophil-basophil carcinoma of pituitary gland", "Mixed acidophil-basophil carcinoma (morphologic abnormality)", "mixed acidophil-basophil carcinoma of pituitary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mixed acidophil-basophil carcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0007278", "names": ["CTAA1", "CTPP5", "CTRCT32", "cataract, anterior polar", "anterior polar cataract 1", "cataract 32 multiple types", "posterior polar cataract 5", "CATARACT 32, MULTIPLE TYPES", "cataract, anterior polar, 1", "cataract 32, multiple types", "CATARACT, POSTERIOR POLAR, 5", "Cataract, posterior polar, 5", "cataract, posterior polar, 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 32 multiple types", "shortest_name_length": 5}
{"curie": "UMLS:C1096400", "names": ["Hemorrhagic transformation stroke", "Haemorrhagic transformation stroke"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemorrhagic transformation stroke", "shortest_name_length": 33}
{"curie": "MONDO:0007664", "names": ["GLC1A", "JOAG1", "GLC1L", "JOAG1A", "MYOC juvenile glaucoma", "Glaucoma 1, Open Angle, A", "GLAUCOMA 1, OPEN ANGLE, A", "glaucoma 1, open angle, A", "GLAUCOMA 1, OPEN ANGLE, L", "glaucoma 1, open angle, 50", "glaucoma hereditary, juvenile", "glaucoma 1, open angle, type A", "glaucoma 1A, primary open angle", "MYOC juvenile open angle glaucoma", "juvenile glaucoma caused by mutation in MYOC", "primary open angle glaucoma juvenile onset 1", "Glaucoma, Primary Open Angle, Juvenile-Onset, 1", "glaucoma, primary open angle, juvenile-onset, 1", "GLAUCOMA, PRIMARY OPEN ANGLE, JUVENILE-ONSET, 1", "juvenile open angle glaucoma caused by mutation in MYOC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glaucoma 1, open angle, A", "shortest_name_length": 5}
{"curie": "MONDO:0017944", "names": ["iNTS disease", "Invasive non-typhoidal Salmonellosis", "Invasive non-typhoidal salmonellosis", "invasive non-typhoidal salmonellosis", "Invasive non-typhoidal salmonella disease", "Salmonella infection non-typhoid invasive", "invasive non-typhoidal salmonella disease", "Invasive non-typhoidal salmonellosis (disorder)", "iNTS (invasive non-typhoidal salmonella) disease", "Invasive non-typhoidal Salmonellosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "invasive non-typhoidal salmonellosis", "shortest_name_length": 12}
{"curie": "MONDO:0020740", "names": ["XHMED", "EDAID1", "Xhm-Ed", "EDA-Id", "HED-Id", "IKBKG/NEMO", "NEMO Deficiency Syndrome", "Ectodermal Dysplasia and Immunodeficiency 1", "ECTODERMAL DYSPLASIA AND IMMUNODEFICIENCY 1", "ectodermal dysplasia and immunodeficiency 1", "ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH IMMUNE DEFICIENCY", "ectodermal dysplasia, anhidrotic, with immune deficiency 1", "ectodermal dysplasia, hypohidrotic, with immune deficiency 1", "ectodermal dysplasia and immunodeficiency 1, X-linked recessive", "HYPER-IgM IMMUNODEFICIENCY, X-LINKED, WITH HYPOHIDROTIC ECTODERMAL DYSPLASIA", "HYPER-IgM IMMUNODEFICIENCY, X-LINKED, WITH ECTODERMAL DYSPLASIA, HYPOHIDROTIC", "Hyper-IgM Immunodeficiency, X-Linked, with Ectodermal Dysplasia, Hypohidrotic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia and immunodeficiency 1", "shortest_name_length": 5}
{"curie": "MONDO:0012983", "names": ["CORD12", "CONE-ROD DYSTROPHY 12", "Cone-Rod Dystrophy 12", "cone-rod dystrophy 12", "PROM1 cone-rod dystrophy", "cone-rod dystrophy type 12", "cone-rod dystrophy caused by mutation in PROM1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cone-rod dystrophy 12", "shortest_name_length": 6}
{"curie": "UMLS:C2983011", "names": ["Stage IV Uterine Corpus Cancer", "Stage IV Uterine Corpus Cancer AJCC v7", "Stage IV Uterine (including Endometrial) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Uterine Corpus Cancer", "shortest_name_length": 30}
{"curie": "UMLS:C0685866", "names": ["HOLORACHISCHISIS", "Holorachischisis", "Rachischisis totalis", "Holorachischisis (disorder)", "Holorachischisis (diagnosis)", "congenital spinal anomaly spina bifida rachischisis holorachischisis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Holorachischisis", "shortest_name_length": 16}
{"curie": "MONDO:0003504", "names": ["anal canal NET", "anus neuroendocrine tumor", "anal neuroendocrine tumor", "anal neuroendocrine tumour", "anal neuroendocrine neoplasm", "Anal Neuroendocrine Neoplasm", "Neuroendocrine tumor of anus", "anus neuroendocrine neoplasm", "neuroendocrine tumor of anus", "Neuroendocrine tumour of anus", "neuroendocrine tumour of anus", "neuroendocrine neoplasm of anus", "Neuroendocrine Neoplasm of Anus", "anal canal neuroendocrine tumor", "Anal Canal Neuroendocrine Neoplasm", "anal canal neuroendocrine neoplasm", "Neuroendocrine Neoplasm of the Anus", "neuroendocrine neoplasm of the anus", "neuroendocrine neoplasm of anal canal", "Neuroendocrine tumor of anus (disorder)", "anal canal neuroendocrine tumor, well differentiated, low or intermediate grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anal canal neuroendocrine neoplasm", "shortest_name_length": 14}
{"curie": "MONDO:0014901", "names": ["STHAG8", "WNT10B tooth agenesis", "tooth agenesis, selective, 8", "TOOTH AGENESIS, SELECTIVE, 8", "tooth agenesis, selective, type 8", "tooth agenesis, selective, 8; STHAG8", "tooth agenesis caused by mutation in WNT10B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tooth agenesis, selective, 8", "shortest_name_length": 6}
{"curie": "MONDO:0001057", "names": ["malignant gastric granular cell tumor", "Malignant Granular Cell Stomach Tumor", "Malignant Gastric Granular Cell Tumor", "malignant granular cell stomach tumor", "malignant gastric granular cell tumour", "Malignant Gastric Granular Cell Neoplasm", "malignant granular cell tumor of stomach", "malignant gastric granular cell neoplasm", "malignant granular cell stomach neoplasm", "Malignant Granular Cell Tumor of Stomach", "Malignant Granular Cell Stomach Neoplasm", "malignant granular cell tumour of stomach", "malignant granular cell neoplasm of stomach", "Malignant Granular Cell Neoplasm of Stomach", "malignant granular cell tumor of the stomach", "Malignant Granular Cell Tumor of the Stomach", "Malignant Granular Cell Neoplasm of the Stomach", "malignant granular cell neoplasm of the stomach"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant gastric granular cell tumor", "shortest_name_length": 37}
{"curie": "UMLS:C4727362", "names": ["Recurrent Ampulla of Vater Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Ampulla of Vater Adenocarcinoma", "shortest_name_length": 41}
{"curie": "UMLS:C3272532", "names": ["Small Intestinal Large Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Intestinal Large Cell Neuroendocrine Carcinoma", "shortest_name_length": 52}
{"curie": "MONDO:0003118", "names": ["testis Brenner tumor", "testicular Brenner tumor", "Testicular Brenner Tumor", "testes, rudimentary Brenner tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular Brenner tumor", "shortest_name_length": 20}
{"curie": "MONDO:0020406", "names": ["CAVC type A", "CAVC-left heart obstruction syndrome", "complete atrioventricular canal type A", "complete atrioventricular canal-left heart obstruction syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complete atrioventricular canal-left heart obstruction syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0007498", "names": ["ear exostoses", "EAR EXOSTOSES", "Swimmers exostosis", "external ear canal; exostosis", "exostosis; external ear canal", "Exostosis of external ear canal", "exostosis of external ear canal", "External auditory canal exostosis", "External auditory canal exostoses", "EXOSTOSES OF EXTERNAL AUDITORY CANAL", "exostoses of external auditory canal", "Exostosis of the external auditory canal", "Exostosis of external ear canal (disorder)", "exostosis of external ear canal (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ear exostoses", "shortest_name_length": 13}
{"curie": "MONDO:0005638", "names": ["Agnosia", "APRAXIA", "Apraxia", "apraxia", "agnosia", "Apraxias", "APRAXIAS", "apraxias", "DYSPRAXIA", "Dyspraxia", "dyspraxia", "dyspraxias", "Dyspraxias", "Apraxia, NOS", "visual amnesia", "Apraxia (finding)", "dyspraxia syndrome", "Dyspraxia syndrome", "Dyspraxia (finding)", "dyspraxia (finding)", "syndrome; dyspraxia", "dyspraxia; syndrome", "primary visual agnosia", "Monomodal visual amnesia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "agnosia", "shortest_name_length": 7}
{"curie": "UMLS:C0334394", "names": ["Adenocarcinoma with osseous metaplasia", "Adenocarcinoma with Osseous Metaplasia", "Adenocarcinoma with Cartilaginous Metaplasia", "Adenocarcinoma with cartilaginous metaplasia", "Adenocarcinoma with Cartilaginous and Osseous Metaplasia", "Adenocarcinoma with cartilaginous and osseous metaplasia", "adenocarcinoma with cartilaginous and osseous metaplasia", "adenocarcinoma with cartilaginous and osseous metaplasia (diagnosis)", "Adenocarcinoma with cartilaginous and osseous metaplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma with cartilaginous and osseous metaplasia", "shortest_name_length": 38}
{"curie": "UMLS:C3544321", "names": ["refractory schizophrenia", "Refractory Schizophrenia", "Schizophrenia, Refractory", "Treatment Resistant Schizophrenia", "Treatment-resistant schizophrenia", "Treatment-Resistant Schizophrenia", "Schizophrenia, Treatment-Resistant", "Schizophrenia, Treatment Resistant", "refractory schizophrenia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Schizophrenia, Treatment-Resistant", "shortest_name_length": 24}
{"curie": "UMLS:C0877854", "names": ["Cerebral Arteriosclerosis", "Cerebral Arterioscleroses", "Cerebral arteriosclerosis", "cerebral; arteriosclerosis", "Arteriosclerosis, Cerebral", "arteriosclerosis; cerebral", "Arterioscleroses, Cerebral", "CEREBROVASCULAR ARTERIOSCLEROSIS", "cerebrovascular; arteriosclerosis", "arteriosclerosis; cerebrovascular", "Cerebral vascular arteriosclerosis", "Cerebral arteriosclerosis (disorder)", "cerebrovascular; disorder, arteriosclerotic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebral Arteriosclerosis", "shortest_name_length": 25}
{"curie": "UMLS:C0686377", "names": ["CNS Metastasis", "CNS METASTASIS", "CNS Metastases", "cns metastases", "CNS metastasis", "CNS metastases", "metastases, CNS", "cns involvement", "Metastatic Tumor to the CNS", "Metastatic Neoplasm to the CNS", "Central Nervous System Metastases", "central nervous system metastasis", "Central Nervous System Metastasis", "central nervous system metastases", "Metastases to central nervous system", "Metastatic Tumor to the Central Nervous System", "Metastatic Neoplasm to the Central Nervous System", "Cancer metastatic to CNS (central nervous system)", "secondary malignant neoplasm central nervous system", "Secondary malignant neoplasm of central nervous system", "Metastatic malignant neoplasm to central nervous system", "Metastatic malignant neoplasm of central nervous system", "Secondary malignant neoplasm of central nervous system, NOS", "Metastatic Malignant Neoplasm to the Central Nervous System", "Metastatic Malignant Neoplasm in the Central Nervous System", "Metastatic malignant neoplasm to central nervous system, NOS", "Metastatic malignant neoplasm to central nervous system (disorder)", "Secondary malignant neoplasm of central nervous system (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CNS metastases", "shortest_name_length": 14}
{"curie": "UMLS:C0751447", "names": ["Preparalytic Poliomyelitis", "Poliomyelitis, Preparalytic", "Poliomyelitides, Preparalytic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Poliomyelitis, Preparalytic", "shortest_name_length": 26}
{"curie": "UMLS:C5550994", "names": ["Malposition of ureter", "Malposition of Ureter", "Malposition of ureter, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malposition of Ureter", "shortest_name_length": 21}
{"curie": "MONDO:0015801", "names": ["hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation", "shortest_name_length": 66}
{"curie": "UMLS:C1504558", "names": ["Subependymal hemorrhage", "Subependymal Hemorrhage", "Subependymal haemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subependymal haemorrhage", "shortest_name_length": 23}
{"curie": "UMLS:C4288806", "names": ["Low Grade Fallopian Tube Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Grade Fallopian Tube Serous Adenocarcinoma", "shortest_name_length": 46}
{"curie": "MONDO:0005037", "names": ["Intestinal", "Intestinal Stomach Adenocarcinoma", "intestinal gastric adenocarcinoma", "intestinal stomach adenocarcinoma", "Intestinal Gastric Adenocarcinoma", "intestinal adenocarcinoma of stomach", "Intestinal Adenocarcinoma of Stomach", "gastric intestinal type adenocarcinoma", "Gastric Intestinal-Type Adenocarcinoma", "Gastric Intestinal Type Adenocarcinoma", "intestinal type stomach adenocarcinoma", "gastric intestinal-type adenocarcinoma", "Intestinal Adenocarcinoma of the Stomach", "intestinal adenocarcinoma of the stomach", "stomach cancer, intestinal adenocarcinoma", "gastric cancer, intestinal adenocarcinoma", "stomach, intestinal adenocarcinoma of the", "Gastric adenocarcinoma of the intestinal type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric intestinal type adenocarcinoma", "shortest_name_length": 10}
{"curie": "MONDO:0006169", "names": ["Complex", "complex endometrial hyperplasia", "endometrial complex hyperplasia", "complex hyperplasia endometrial", "Complex Endometrial Hyperplasia", "Complex endometrial hyperplasia", "Endometrial Hyperplasia, Complex", "Hyperplasia, Complex Endometrial", "Complex Endometrial Hyperplasias", "Glandular endometrial hyperplasia", "Endometrial glandular hyperplasia", "Endometrial Hyperplasias, Complex", "Hyperplasias, Complex Endometrial", "ENDOMETRIUM HYPERPLASIA ADENOMATOUS", "adenomatous endometrial hyperplasia", "Adenomatoid endometrial hyperplasia", "Adenomatous endometrial hyperplasia", "Endometrial adenomatous hyperplasia", "Adenomatous hyperplasia of endometrium", "Complex endometrial hyperplasia (disorder)", "complex endometrial hyperplasia (diagnosis)", "uterus; hyperplasia, endometrial (glandular)", "hyperplasia; uterus, endometrial (glandular)", "adenomatous endometrial hyperplasia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complex endometrial hyperplasia", "shortest_name_length": 7}
{"curie": "MONDO:0006940", "names": ["Radial nerve lesion", "radial nerve lesion", "lesion radial nerve", "Radial nerve lesions", "lesions nerve radial", "radial nerve lesions", "lesion of radial nerve", "Lesion of radial nerve", "Radial nerve lesion NOS", "Lesion of radial nerve, NOS", "Lesion of radial nerve (disorder)", "radial nerve peripheral nerve lesion", "peripheral nerve lesion of radial nerve", "Lesion of radial nerve, unspecified upper limb"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radial nerve lesion", "shortest_name_length": 19}
{"curie": "UMLS:C4521635", "names": ["Stage IVB Laryngeal Throat Cancer", "Stage IVB Laryngeal Cancer AJCC v8", "Stage IVB Laryngeal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Laryngeal Cancer AJCC v8", "shortest_name_length": 33}
{"curie": "MONDO:0021758", "names": ["ANGINA AGRANULOCYTIC", "Agranulocytic angina", "agranulocytic angina", "Angina agranulocytic", "AGRANULOCYTIC ANGINA", "Agranulocytic Angina", "agranulocytic; angina", "ANGINA, AGRANULOCYTIC", "angina; agranulocytic", "neutropenia, malignant", "Acquired agranulocytosis", "acquired agranulocytosis", "granulocytopenia, primary", "agranulocytosis, acquired"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired agranulocytosis", "shortest_name_length": 20}
{"curie": "MONDO:0001718", "names": ["Scleritis", "scleritis", "SCLERITIS", "Scleritides", "Scleritis NOS", "Scleritis, NOS", "scleritis (disease)", "Scleritis (disorder)", "scleritis (diagnosis)", "Unspecified scleritis", "Inflammation of sclera", "Scleritis, unspecified", "Inflammation of white of eye", "scleritis (physical finding)", "Inflammation of the outer white part of the eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scleritis", "shortest_name_length": 9}
{"curie": "MONDO:0003792", "names": ["ovarian MMMT", "Ovarian MMMT", "MMMT of the ovary", "ovary carcinosarcoma", "Ovarian carcinosarcoma", "ovarian carcinosarcoma", "Ovarian Carcinosarcoma", "Carcinosarcoma of ovary", "carcinosarcoma, ovarian", "Carcinosarcoma of Ovary", "carcinosarcoma of ovary", "carcinosarcoma of the ovary", "Carcinosarcoma of the Ovary", "Carcinosarcoma of ovary (disorder)", "carcinosarcoma of ovary (diagnosis)", "Ovarian Malignant Mixed Müllerian Tumor", "ovarian malignant mixed Müllerian tumor", "Ovarian Malignant Mixed Mullerian Tumor", "ovarian malignant mixed Mullerian tumor", "Ovarian malignant mixed Müllerian tumor", "ovarian malignant mixed Mullerian neoplasm", "Ovarian Malignant Mixed Müllerian Neoplasm", "ovarian malignant mixed Müllerian neoplasm", "Ovarian Malignant Mixed Mullerian Neoplasm", "malignant mixed Müllerian tumor of the ovary", "Malignant mixed Müllerian tumor of the ovary", "Ovarian Malignant Mixed Mesodermal Mullerian Tumor", "Ovarian Malignant Mixed Mesodermal Müllerian Tumor", "ovarian malignant mixed mesodermal Müllerian tumor", "ovarian malignant mixed mesodermal Mullerian tumor", "Malignant Mixed Mesodermal Müllerian Tumor of Ovary", "malignant mixed mesodermal Mullerian tumor of ovary", "malignant mixed mesodermal Mullerian tumor, ovarian", "Malignant Mixed Mesodermal Mullerian Tumor of Ovary", "malignant mixed mesodermal Müllerian tumor of ovary", "Mullerian tumor, ovarian malignant mixed mesodermal", "ovarian malignant mesodermal (Mullerian) mixed tumor", "Ovarian Malignant Mixed Mesodermal (Müllerian) Tumor", "Ovarian Malignant Mixed Mesodermal (Mullerian) Tumor", "Ovarian Malignant Mesodermal (Mullerian) Mixed Tumor", "ovarian malignant mixed mesodermal (Müllerian) tumor", "ovarian malignant mesodermal (mullerian) mixed tumor", "ovarian malignant mesodermal (Müllerian) mixed tumor", "Ovarian Malignant Mesodermal (Müllerian) Mixed Tumor", "ovarian malignant mixed epithelial mesenchymal tumor", "Ovarian malignant mixed epithelial mesenchymal tumor", "ovarian malignant mixed mesodermal (Mullerian) tumor", "Ovarian Malignant Mixed Mesodermal Mullerian Neoplasm", "ovarian malignant mixed mesodermal Müllerian neoplasm", "ovarian malignant mixed mesodermal Mullerian neoplasm", "Ovarian Malignant Mixed Mesodermal Müllerian Neoplasm", "Mullerian sarcoma, ovarian malignant mixed mesodermal", "Malignant Mixed Mesodermal Müllerian Neoplasm of Ovary", "malignant mixed mesodermal Müllerian neoplasm of ovary", "malignant mixed mesodermal Mullerian neoplasm of ovary", "Malignant Mixed Mesodermal Mullerian Neoplasm of Ovary", "ovarian carcinosarcoma/malignant mixed mesodermal tumor", "malignant mixed mesodermal Müllerian tumor of the ovary", "Malignant Mixed Mesodermal Mullerian Tumor of the Ovary", "Malignant Mixed Mesodermal Müllerian Tumor of the Ovary", "malignant mixed mesodermal Mullerian tumor of the ovary", "malignant mixed mesodermal Müllerian neoplasm of the ovary", "Malignant Mixed Mesodermal Mullerian Neoplasm of the Ovary", "Malignant Mixed Mesodermal Müllerian Neoplasm of the Ovary", "malignant mixed mesodermal Mullerian neoplasm of the ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian carcinosarcoma", "shortest_name_length": 12}
{"curie": "UMLS:C5418901", "names": ["Resectable Platinum-Resistant Malignant Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Platinum-Resistant Malignant Germ Cell Tumor", "shortest_name_length": 55}
{"curie": "MONDO:0002357", "names": ["hepatic flexure cancer", "Ca hepatic flexure - colon", "Hepatic flexure colon cancer", "COLON HEPATIC FLEXURE CANCER", "hepatic flexure of colon cancer", "cancer of hepatic flexure of colon", "Malignant tumor of hepatic flexure", "malignant tumor of hepatic flexure", "Malignant tumour of hepatic flexure", "malignant neoplasm of hepatic flexure", "Malignant neoplasm of hepatic flexure", "malignant hepatic flexure of colon neoplasm", "Malignant tumor of hepatic flexure (disorder)", "Malignant neoplasm of hepatic flexure of colon", "malignant neoplasm of hepatic flexure of colon", "malignant neoplasm of hepatic flexure (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatic flexure cancer", "shortest_name_length": 22}
{"curie": "MONDO:0006713", "names": ["pannus", "Pannus", "Pannus of eye", "Ocular pannus", "corneal pannus", "Corneal pannus", "Corneal Pannus", "Pannus, corneal", "Pannus formation", "Pannus (corneal)", "Pannus Formation", "Corneal Angiogenesis", "Angiogenesis, Corneal", "Corneal vascularization", "CORNEAL VASCULARIZATION", "corneal vascularization", "Corneal vascularisation", "Pannus of eye (disorder)", "Vascularisation of cornea", "Corneal pannus (disorder)", "Vascularization of cornea", "Limbal neovascularization", "corneal neovascularization", "corneal pannus (diagnosis)", "corneal neovascularisation", "Corneal Neovascularization", "Corneal neovascularization", "neovascularization; cornea", "cornea; neovascularization", "Corneal neovascularisation", "Corneal Neovascularizations", "Neovascularization, Corneal", "Neovascularizations, Corneal", "neovascularization of cornea", "Corneal neovascularization, NOS", "corneal pannus (physical finding)", "Vascularization of cornea (disorder)", "New blood vessel formation in cornea", "Unspecified corneal neovascularization", "corneal neovascularization (diagnosis)", "Corneal neovascularization, unspecified", "Extensive superficial corneal vascularisation", "Extensive superficial corneal vascularization", "neovascularization of cornea (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal neovascularization", "shortest_name_length": 6}
{"curie": "MONDO:0000945", "names": ["Insufficiency;venous", "VENOUS INSUFFICIENCY", "insufficiency venous", "Venous Insufficiency", "venous insufficiency", "Venous insufficiency", "insufficiency; venous", "venous; insufficiency", "Insufficiency, Venous", "Venous Insufficiencies", "Insufficiencies, Venous", "Poorly functioning veins", "VENOUS INSUFFICIENCY CHRONIC", "venous insufficiency (disease)", "Venous peripheral insufficiency", "peripheral venous insufficiency", "Peripheral venous insufficiency", "venous insufficiency (diagnosis)", "Venous insufficiency, unspecified", "Peripheral venous insufficiency, NOS", "Peripheral venous insufficiency (disorder)", "peripheral venous insufficiency (diagnosis)", "Peripheral venous insufficiency, unspecified", "Venous (peripheral) insufficiency, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "venous insufficiency", "shortest_name_length": 20}
{"curie": "MONDO:0010954", "names": ["WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT", "Wiskott-Aldrich syndrome, autosomal dominant form", "Wiskott-Aldrich Syndrome, Autosomal Dominant Form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wiskott-Aldrich syndrome, autosomal dominant form", "shortest_name_length": 44}
{"curie": "MONDO:0017603", "names": ["ALK- ALCL", "ALCL, ALK-", "ALK- anaplastic large cell lymphoma", "ALK-Negative Anaplastic Large Cell Lymphoma", "lymphoma anaplastic large cell ALK-negative", "ALK negative anaplastic large cell lymphoma", "ALK-negative anaplastic large cell lymphoma", "Anaplastic large cell lymphoma, ALK-negative", "Anaplastic Large Cell Lymphoma, ALK-Negative", "anaplastic large cell lymphoma, ALK-negative", "Anaplastic large cell lymphoma, ALK negative", "ALK-negative anaplastic large cell lymphoma (diagnosis)", "Anaplastic lymphoma kinase negative anaplastic large cell lymphoma", "Anaplastic large cell lymphoma, ALK (anaplastic lymphoma kinase) negative", "Anaplastic lymphoma kinase negative anaplastic large cell lymphoma (disorder)", "Anaplastic lymphoma kinase negative anaplastic large cell lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ALK-negative anaplastic large cell lymphoma", "shortest_name_length": 9}
{"curie": "UMLS:C3896643", "names": ["NODAT", "New Onset Diabetes After Transplant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "New Onset Diabetes After Transplant", "shortest_name_length": 5}
{"curie": "UMLS:C3658266", "names": ["Androgen-Resistant Prostatic Cancer", "Hormone Refractory Prostatic Cancer", "Androgen Resistant Prostatic Cancer", "Cancer, Androgen-Resistant Prostatic", "Androgen-Resistant Prostatic Cancers", "Prostatic Cancer, Hormone Refractory", "Prostatic Cancer, Androgen-Resistant", "Prostatic Cancer, Androgen Resistant", "Androgen-Insensitive Prostatic Cancer", "Cancers, Androgen-Resistant Prostatic", "Castration-Resistant Prostatic Cancer", "Androgen Independent Prostatic Cancer", "Androgen Insensitive Prostatic Cancer", "Prostatic Cancers, Androgen-Resistant", "Androgen-Independent Prostatic Cancer", "Castration Resistant Prostatic Cancer", "Prostatic Cancer, Castration Resistant", "Cancer, Castration-Resistant Prostatic", "Prostatic Cancer, Androgen Independent", "Cancer, Androgen-Insensitive Prostatic", "Prostatic Cancer, Castration-Resistant", "Prostatic Cancer, Androgen-Independent", "Cancer, Androgen-Independent Prostatic", "Castration-Resistant Prostatic Cancers", "Prostatic Cancer, Androgen-Insensitive", "Androgen-Insensitive Prostatic Cancers", "Androgen-Independent Prostatic Cancers", "Prostatic Cancer, Androgen Insensitive", "Prostatic Cancers, Castration-Resistant", "Prostatic Cancers, Androgen-Insensitive", "Cancers, Androgen-Independent Prostatic", "Cancers, Castration-Resistant Prostatic", "Prostatic Cancers, Androgen-Independent", "Cancers, Androgen-Insensitive Prostatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostatic Cancer, Castration-Resistant", "shortest_name_length": 35}
{"curie": "MONDO:0014161", "names": ["VUR7", "VESICOURETERAL REFLUX 7", "vesicoureteral reflux 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vesicoureteral reflux 7", "shortest_name_length": 4}
{"curie": "UMLS:C0857493", "names": ["Upper gastrointestinal symptoms"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Upper gastrointestinal symptoms", "shortest_name_length": 31}
{"curie": "MONDO:0017440", "names": ["humeral agenesis/hypoplasia", "congenital absence of humerus", "humeral intercalary meromelia", "congenital hypoplasia of humerus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "humeral agenesis/hypoplasia", "shortest_name_length": 27}
{"curie": "UMLS:C4552933", "names": ["Stage II Differentiated Thyroid Gland Cancer", "Stage II Differentiated Thyroid Gland Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Differentiated Thyroid Gland Carcinoma AJCC v8", "shortest_name_length": 44}
{"curie": "UMLS:C5418796", "names": ["Locally Advanced Vaginal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Vaginal Carcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0010860", "names": ["NSRD3", "NRSD3", "DFNB3", "deafness, autosomal recessive 3", "Deafness, Autosomal Recessive 3", "DEAFNESS, AUTOSOMAL RECESSIVE 3", "deafness, autosomal recessive type 3", "autosomal recessive nonsyndromic deafness 3", "neurosensory nonsyndromic recessive deafness 3", "Neurosensory Nonsyndromic Recessive Deafness 3", "NEUROSENSORY NONSYNDROMIC RECESSIVE DEAFNESS 3", "autosomal recessive nonsyndromic hearing loss 3", "MYO15A autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic deafness type 3", "autosomal recessive nonsyndromic deafness caused by mutation in MYO15A", "autosomal recessive deafness 3, neurosensory nonsyndromic recessive deafness 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 3", "shortest_name_length": 5}
{"curie": "MONDO:0000162", "names": ["autoimmune thyroid disease, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune thyroid disease, susceptibility to", "shortest_name_length": 45}
{"curie": "UMLS:C0339219", "names": ["Ulcerative keratitis", "KERATITIS ULCERATIVE", "ulcerative; keratitis", "Inflammatory corneal ulcer", "Ulcerative keratitis (disorder)", "Inflammatory corneal ulcer (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Inflammatory corneal ulcer", "shortest_name_length": 20}
{"curie": "MONDO:0016598", "names": ["autosomal recessive secondary polycythemia, non-Chuvash type", "autosomal recessive secondary erythrocytosis, non-Chuvash type", "autosomal recessive secondary polycythemia not associated with VHL gene", "autosomal recessive secondary erythrocytosis not associated with VHL gene"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive secondary polycythemia not associated with VHL gene", "shortest_name_length": 60}
{"curie": "MONDO:0016319", "names": ["congenital analgesia with hyperhidrosis", "congenital absence of pain with hyperhidrosis", "congenital indifference to pain with hyperhidrosis", "congenital insensitivity to pain with hyperhidrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital insensitivity to pain with hyperhidrosis", "shortest_name_length": 39}
{"curie": "MONDO:0001335", "names": ["EYELASH SCANTINESS", "eyelid hypotrichosis", "Hypotrichosis of eyelid", "hypotrichosis of eyelid", "eyelid disorder hypotrichosis", "Hypotrichosis of eyelid (disorder)", "hypotrichosis of eyelid (diagnosis)", "hypotrichosis of eyelid (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotrichosis of eyelid", "shortest_name_length": 18}
{"curie": "MONDO:0018034", "names": ["Lenz's syndrome", "thalidomide syndrome", "Wiedemann's syndrome", "Thalidomide Embryopathy", "Thalidomide embryopathy", "thalidomide embryopathy", "Fetal Thalidomide Syndrome", "Fetal thalidomide syndrome", "fetal thalidomide syndrome", "Foetal thalidomide syndrome", "Thalidomide embryopathy syndrome", "thalidomide-induced birth defect", "thalidomide syndrome (diagnosis)", "Thalidomide Embryopathy Syndrome", "thalidomide embryopathy syndrome", "Thalidomide-Induced Birth Defect", "Congenital malformation due to thalidomide", "Thalidomide embryopathy syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thalidomide embryopathy", "shortest_name_length": 15}
{"curie": "UMLS:C2825739", "names": ["Fibroblastic reticular cell tumor", "Fibroblastic Reticular Cell Tumor", "Fibroblastic reticular cell tumour", "Fibroblastic reticular cell neoplasm", "Fibroblastic reticular cell neoplasm (disorder)", "Fibroblastic reticular cell neoplasm (diagnosis)", "Fibroblastic reticular cell tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fibroblastic reticular cell neoplasm", "shortest_name_length": 33}
{"curie": "UMLS:C5420223", "names": ["Oral Squamous Cell Papilloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral Squamous Cell Papilloma", "shortest_name_length": 28}
{"curie": "MONDO:0001133", "names": ["Malignant Essential Hypertension", "Malignant essential hypertension", "malignant essential hypertension", "Essential hypertension, malignant", "accelerated essential hypertension", "Accelerated essential hypertension", "Malignant essential hypertension (disorder)", "malignant essential hypertension (diagnosis)", "accelerated essential hypertension (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant essential hypertension", "shortest_name_length": 32}
{"curie": "MONDO:0002408", "names": ["hyperbilirubinemia", "hyperbilirubinaemia", "bilirubin metabolic disorder", "Hereditary Hyperbilirubinemia", "hereditary hyperbilirubinemia", "Hereditary Hyperbilirubinemias", "Hyperbilirubinemia, Hereditary", "Hyperbilirubinemias, Hereditary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary hyperbilirubinemia", "shortest_name_length": 18}
{"curie": "UMLS:C1336200", "names": ["Stage IIC Ovarian Germ Cell Tumor", "Stage IIC Ovarian Germ Cell Tumor AJCC v7", "Stage IIC Ovarian Germ Cell Tumor AJCC v6", "FIGO Stage IIC Malignant Ovarian Germ Cell Tumor", "Stage IIC Ovarian Germ Cell Tumor AJCC v6 and v7", "FIGO Stage IIC Malignant Germ Cell Tumor of Ovary", "FIGO Stage IIC Malignant Ovarian Germ Cell Neoplasm", "FIGO Stage IIC Malignant Germ Cell Neoplasm of Ovary", "FIGO Stage IIC Malignant Germ Cell Tumor of the Ovary", "FIGO Stage IIC Malignant Germ Cell Neoplasm of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIC Ovarian Germ Cell Tumor AJCC v6 and v7", "shortest_name_length": 33}
{"curie": "MONDO:0044306", "names": ["NECFM", "NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION", "severe neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataract", "neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination", "shortest_name_length": 5}
{"curie": "UMLS:C1334763", "names": ["Midgut Carcinoid Tumor", "Midgut Neuroendocrine Tumor G1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Midgut Neuroendocrine Tumor G1", "shortest_name_length": 22}
{"curie": "MONDO:0001315", "names": ["nervous heart", "Cardioneurosis", "cardioneurosis", "HEART, NERVOUS", "Cardiac Phobia", "SYNDROME EFFORT", "Effort Syndrome", "Phobia, Cardiac", "effort syndrome", "Effort syndrome", "Syndrome effort", "EFFORT SYNDROME", "Neurosis;cardiac", "Cardiac Neuroses", "CARDIAC NEUROSIS", "Cardiac Neurosis", "cardiac neuroses", "Cardiac neurosis", "Syndrome, Effort", "cardiac neurosis", "Neurosis, Cardiac", "da costa syndrome", "DA COSTA SYNDROME", "costas da syndrome", "Krishaber's disease", "Da Costa's syndrome", "da costa's syndrome", "Cerebrocardiac syndrome", "cardiovascular neurosis", "Cardiovascular neurosis", "NEUROSIS CARDIOVASCULAR", "Cerebrocardiac neurosis", "Neurosis cardiovascular", "Neurosis, cerebrocardiac", "Irritable heart syndrome", "Neurocirculatory Asthenia", "neurocirculatory asthenia", "Neurocirculatory asthenia", "NEUROCIRCULATORY ASTHENIA", "Neurocirculatory Asthenias", "Asthenia, Neurocirculatory", "cardiac neurosis (diagnosis)", "FUNCTIONAL CARDIOVASCULAR DISEASE", "Cardiovascular disorder, psychogenic", "Neurocirculatory asthenia (disorder)", "cardiovascular malfunction arising from mental factors", "Cardiovascular malfunction arising from mental factors"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurocirculatory asthenia", "shortest_name_length": 13}
{"curie": "UMLS:C0393693", "names": ["Benign Neonatal Nonfamilial Epilepsy", "Non Familial Benign Neonatal Epilepsy", "Benign Neonatal Epilepsy, Nonfamilial", "Non-Familial Benign Neonatal Epilepsy", "Epilepsy, Benign Neonatal, Nonfamilial", "Epilepsy, Benign Neonatal, Non-Familial", "Benign Neonatal Non-Familial Convulsions", "Benign non-familial neonatal convulsions", "Benign Non-Familial Neonatal Convulsions", "Non Familial Benign Neonatal Convulsions", "Benign Neonatal Non Familial Convulsions", "Benign Non Familial Neonatal Convulsions", "Non-Familial Benign Neonatal Convulsions", "Convulsions, Benign Neonatal, Non-Familial", "Benign non-familial neonatal convulsions (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Neonatal Epilepsy, Nonfamilial", "shortest_name_length": 36}
{"curie": "MONDO:0006053", "names": ["renal leiomyoma", "kidney leiomyoma", "leiomyoma of kidney"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal leiomyoma", "shortest_name_length": 15}
{"curie": "MONDO:0017958", "names": ["magic syndrome", "mouth and genital ulcers with inflamed cartilage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "magic syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C3697841", "names": ["Salivary Gland Hemangioma", "Hemangioma of salivary gland", "Haemangioma of salivary gland", "Hemangioma of salivary gland (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemangioma of salivary gland", "shortest_name_length": 25}
{"curie": "MONDO:0017931", "names": ["HIBM4", "hereditary inclusion body myopathy type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary inclusion body myopathy type 4", "shortest_name_length": 5}
{"curie": "MONDO:0021168", "names": ["Hibernoma", "hibernoma", "hibernomas", "Hibernomas", "Brown fat tumor", "Brown Fat Tumor", "Brown fat tumour", "hibernoma, benign", "HIBERNOMA, BENIGN", "Brown fat neoplasm", "Brown Fat Neoplasm", "Granular cell lipoma", "Hibernoma (disorder)", "Fetal fat cell lipoma", "fetal fat cell lipoma", "Fetal Fat Cell Lipoma", "Foetal fat cell lipoma", "fat cells; fetal lipoma", "fetal; lipoma, fat cells", "lipoma; fat cells, fetal", "lipoma; fetal, fat cells", "fat cells; lipoma, fetal", "Hibernoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hibernoma", "shortest_name_length": 9}
{"curie": "MONDO:0009815", "names": ["ARO1", "OPTB1", "Autosomal Recessive Marble Bones", "marble bones autosomal recessive", "marble bones, autosomal recessive", "Marble Bones, Autosomal Recessive", "MARBLE BONES, AUTOSOMAL RECESSIVE", "infantile malignant osteopetrosis 1", "Autosomal Recessive Osteopetrosis 1", "osteopetrosis infantile malignant 1", "Infantile Malignant Osteopetrosis 1", "osteopetrosis autosomal recessive 1", "autosomal recessive osteopetrosis 1", "OSTEOPETROSIS, INFANTILE MALIGNANT 1", "OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1", "osteopetrosis, infantile malignant 1", "osteopetrosis, autosomal recessive 1", "Osteopetrosis, Infantile Malignant 1", "Osteopetrosis, Autosomal Recessive 1", "TCIRG1 autosomal recessive osteopetrosis", "Autosomal Recessive Osteopetrosis Type 1", "autosomal recessive osteopetrosis type 1", "osteopetrosis, autosomal recessive type 1", "autosomal recessive Albers-Schonberg disease", "Autosomal Recessive Albers-Schonberg Disease", "ALBERS-SCHONBERG DISEASE, AUTOSOMAL RECESSIVE", "Albers-Schonberg disease, autosomal recessive", "Albers-Schonberg Disease, Autosomal Recessive", "TCIRG1 autosomal recessive malignant osteopetrosis", "autosomal recessive osteopetrosis caused by mutation in TCIRG1", "autosomal recessive malignant osteopetrosis caused by mutation in TCIRG1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive osteopetrosis 1", "shortest_name_length": 4}
{"curie": "MONDO:0004586", "names": ["Rheumatoid lung", "rheumatoid lung", "LUNG, RHEUMATOID", "lungs rheumatoid", "Rheumatoid lung disease", "LUNG DISEASE RHEUMATOID", "rheumatoid lung disease", "rheumatoid; lung (etiology)", "lung; rheumatoid (etiology)", "rheumatoid; lung (manifestation)", "lung; rheumatoid (manifestation)", "Rheumatoid lung disease (disorder)", "rheumatoid lung disease (diagnosis)", "Rheumatoid lung disease, site unspecified", "rheumatoid arthritis interstitial lung disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rheumatoid lung disease", "shortest_name_length": 15}
{"curie": "UMLS:C1335780", "names": ["Central Nervous System Rhabdomyoma", "Rhabdomyoma of Central Nervous System", "Rhabdomyoma of the Central Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Rhabdomyoma", "shortest_name_length": 34}
{"curie": "UMLS:C0751889", "names": ["Pontine Tumor", "pontine tumor", "Pontine Tumors", "pontine tumors", "Tumor, Pontine", "Tumors, Pontine", "Pontine Neoplasm", "pontine neoplasm", "Neoplasm, Pontine", "Pontine Neoplasms", "Neoplasms, Pontine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pontine Tumors", "shortest_name_length": 13}
{"curie": "MONDO:0019029", "names": ["SOD", "segmental odontomaxillary dysplasia", "Segmental odontomaxillary dysplasia", "Segmental odontomaxillary dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "segmental odontomaxillary dysplasia", "shortest_name_length": 3}
{"curie": "MONDO:0008596", "names": ["TRPS1", "TRPS 1", "TRPS I", "Giedion syndrome", "Sugio-Kajii syndrome", "trichorhinophalangeal syndrome 1", "Trichorhinophalangeal syndrome I", "trichorhinophalangeal dysplasia 1", "Trichorhinophalangeal dysplasia 1", "trichorhinophalangeal syndrome type I", "Trichorhinophalangeal Syndrome Type I", "trichorhinophalangeal syndrome type 1", "type I trichorhinophalangeal syndrome", "TRICHORHINOPHALANGEAL SYNDROME, TYPE I", "trichorhinophalangeal dysplasia type I", "Trichorhinophalangeal Syndrome, Type I", "Trichorhinophalangeal (TRP) syndrome 1", "Trichorhinophalangeal dysplasia type I", "trichorhinophalangeal syndrome, type 1", "trichorhinophalangeal syndrome, type I", "type III trichorhinophalangeal syndrome", "TRPS I - Trichorhinophalangeal syndrome I", "trichorhinophalangeal (TRP) syndrome 1 (TRPS1)", "Trichorhinophalangeal dysplasia type I (disorder)", "Trichorhinophalangeal dysplasia type I (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichorhinophalangeal syndrome type I", "shortest_name_length": 5}
{"curie": "MONDO:0013138", "names": ["BRV2", "vertigo, benign recurrent, 2", "Vertigo, Benign Recurrent, 2", "VERTIGO, BENIGN RECURRENT, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vertigo, benign recurrent, 2", "shortest_name_length": 4}
{"curie": "UMLS:C3898655", "names": ["Myocardial infarction type 4a", "TYPE 4A MYOCARDIAL INFARCTION", "Joint Task Force Type 4A Myocardial Infarction", "Joint ESC/ACCF/AHA/WHF Task Force Type 4A Myocardial Infarction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joint Task Force Type 4A Myocardial Infarction", "shortest_name_length": 29}
{"curie": "MONDO:0001357", "names": ["ANEMIA HYPOCHROMIC", "Anemia hypochromic", "Hypochromic Anemia", "hypochromic anemia", "Hypochromic anemia", "anemia hypochromic", "HYPOCHROMIC ANEMIA", "anemia; hypochromic", "Anemia, Hypochromic", "hypochromic anemias", "hypochromic anaemia", "Hypochromic Anemias", "Hypochromic anaemia", "Anaemia hypochromic", "ANAEMIA HYPOCHROMIC", "Anemias, Hypochromic", "Hypochromic anemia, NOS", "Hypochromic anaemia, NOS", "hypochromic anemia (disease)", "ANEMIA NORMOCYTIC HYPOCHROMIC", "normocytic hypochromic anemia", "Normocytic hypochromic anemia", "Normocytic hypochromic anaemia", "Normocytic hypochromic anemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypochromic anemia", "shortest_name_length": 18}
{"curie": "MONDO:0012113", "names": ["EIG3", "idiopathic generalized epilepsy 3", "epilepsy, idiopathic generalized, susceptibility to, 3", "EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 3", "EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, LOCUS ON CHROMOSOME 9", "epilepsy, idiopathic generalized, susceptibility to, locus on chromosome 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, idiopathic generalized, susceptibility to, 3", "shortest_name_length": 4}
{"curie": "MONDO:0000253", "names": ["piedra", "Piedra", "piedras", "Piedras", "White piedra", "black piedra", "piedra, black", "black Piedras", "White Piedras", "piedra, White", "Piedras, black", "Piedras, White", "steroid-modified tinea infection", "hair shaft fungal infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "piedra", "shortest_name_length": 6}
{"curie": "MONDO:0035735", "names": ["AHA", "acquired hemophilia A", "Acquired hemophilia A", "Hemophilia A, acquired", "Acquired F8 deficiency", "Factor 8 deficiency, acquired", "Acquired factor VIII deficiency", "Acquired Factor VIII Deficiency", "Factor VIII deficiency, acquired", "Acquired factor VIII deficiency disease", "Acquired factor VIII deficiency disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired hemophilia A", "shortest_name_length": 3}
{"curie": "MONDO:0010061", "names": ["SCAR3", "SCABD", "autosomal recessive spinocerebellar ataxia 3", "spinocerebellar ataxia autosomal recessive 3", "spinocerebellar ataxia, autosomal recessive 3", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 3", "Spinocerebellar ataxia, autosomal recessive 3", "Autosomal recessive spinocerebellar ataxia type 3", "autosomal recessive spinocerebellar ataxia type 3", "spinocerebellar ataxia with blindness and deafness", "Spinocerebellar ataxia with blindness and deafness", "SPINOCEREBELLAR ATAXIA WITH BLINDNESS AND DEAFNESS", "SCAR3 - spinocerebellar ataxia autosomal recessive type 3", "autosomal recessive cerebellar ataxia - blindness - deafness", "autosomal recessive cerebellar ataxia-blindness-deafness syndrome", "autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome", "Autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome", "Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome", "autosomal recessive spinocerebellar ataxia-blindness-hearing loss syndrome", "Autosomal recessive spinocerebellar ataxia-blindness-hearing loss syndrome", "Autosomal recessive spinocerebellar ataxia, blindness, hearing loss syndrome", "Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive cerebellar ataxia-blindness-deafness syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C5237018", "names": ["Refractory Diffuse Large B-Cell Lymphoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Diffuse Large B-Cell Lymphoma, Not Otherwise Specified", "shortest_name_length": 65}
{"curie": "MONDO:0017256", "names": ["Anterior uveitis idiopathic", "uveitis anterior idiopathic", "idiopathic anterior uveitis", "Idiopathic anterior uveitis", "Idiopathic anterior uveitis (diagnosis)", "Idiopathic inflammation of anterior uveal tract", "Idiopathic inflammation of anterior uveal tract (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic anterior uveitis", "shortest_name_length": 27}
{"curie": "MONDO:0001014", "names": ["CLL", "CML", "Chronic Leukemia", "CHRONIC LEUKEMIA", "Leukemia chronic", "leukemia chronic", "LEUKEMIA CHRONIC", "Chronic leukemia", "chronic leukemia", "leukemia, chronic", "Chronic leukaemia", "chronic leukaemia", "chronic; leukemia", "leukemia; chronic", "chronic leukemias", "Leukaemia chronic", "Chronic leukemia NOS", "Chronic blood cancer", "Chronic leukemia, NOS", "Chronic leukaemia NOS", "adult chronic leukemia", "Chronic leukaemia, NOS", "Chronic leukemia, disease", "Chronic leukaemia, disease", "chronic leukemia (disease)", "leukemia (disease), chronic", "chronic leukemia (diagnosis)", "Chronic leukemia, disease (disorder)", "Chronic leukemia of unspecified cell type", "Chronic leukemia (morphologic abnormality)", "Chronic leukaemia of unspecified cell type", "Leukemia of unspecified cell type, chronic", "Leukaemia of unspecified cell type, chronic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic leukemia", "shortest_name_length": 3}
{"curie": "UMLS:C2609041", "names": ["Mechanical urticaria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mechanical urticaria", "shortest_name_length": 20}
{"curie": "UMLS:C0454606", "names": ["Oral dyskinesia", "Oral Dyskinesia", "Oral Dyskinesias", "Dyskinesia, Oral", "Dyskinesias, Oral", "Oral dyskinesia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral Dyskinesia", "shortest_name_length": 15}
{"curie": "MONDO:0000870", "names": ["FAB Ll", "childhood all", "childhood ALL", "Pediatric ALL", "Childhood ALL", "pediatric ALL", "pediatric all", "ALL, childhood", "ALL, pediatric", "ALL, Childhood", "L1 Lymphocytic Leukemia", "Lymphocytic Leukemia, L1", "Leukemia, L1 Lymphocytic", "L1 Acute Lymphoblastic Leukemia", "Leukemia, Lymphocytic, Acute, L1", "Lymphoblastic Leukemia, Acute, L1", "Pediatric Acute Lymphoid Leukemia", "childhood acute lymphoid leukemia", "Childhood Acute Lymphoid Leukemia", "pediatric acute lymphoid leukemia", "Acute Lymphoblastic Leukemia (ALL)", "acute lymphoblastic leukemia (ALL)", "Leukemia, Lymphoblastic, Acute, L1", "Childhood Acute Lymphocytic Leukemia", "pediatric acute lymphocytic leukemia", "Pediatric Acute Lymphocytic Leukemia", "childhood acute lymphocytic leukemia", "childhood acute lymphogenous leukemia", "pediatric acute lymphogenous leukemia", "Pediatric Acute Lymphogenous Leukemia", "Childhood Acute Lymphogenous Leukemia", "Childhood Acute Lymphoblastic Leukemia", "Pediatric Acute Lymphoblastic Leukemia", "pediatric acute lymphoblastic leukemia", "childhood acute lymphoblastic leukemia", "childhood leukemia, acute lymphoblastic", "acute lymphoblastic leukemia, childhood", "acute lymphoblastic leukemia, pediatric", "Lymphoblastic Leukemia, Acute, Childhood", "Leukemia, acute lymphocytic (ALL), child", "leukemia, acute lymphoblastic, pediatric", "leukemia, acute lymphoblastic, childhood", "lymphoblastic leukemia, acute, pediatric", "lymphoblastic leukemia, acute, childhood", "Childhood Precursor Lymphoblastic Leukemia", "pediatric acute lymphocytic leukemia (ALL)", "childhood precursor lymphoblastic leukemia", "Pediatric Acute Lymphocytic Leukemia (ALL)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood acute lymphoblastic leukemia", "shortest_name_length": 6}
{"curie": "UMLS:C0749087", "names": ["SUBCLAVIAN VEIN THROMBOSIS", "subclavian vein thrombosis", "Subclavian vein thrombosis", "Thrombosis of subclavian vein", "thrombosis of subclavian veins", "Thrombosis of subclavian vein (disorder)", "thrombosis of subclavian veins (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thrombosis of subclavian vein", "shortest_name_length": 26}
{"curie": "UMLS:C4721923", "names": ["stage IA uterine sarcoma", "Stage IA Uterine Sarcoma", "Stage IA Uterine Sarcoma AJCC v7", "stage IA uterine sarcoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Uterine Sarcoma AJCC v7", "shortest_name_length": 24}
{"curie": "MONDO:0031439", "names": ["short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies", "shortest_name_length": 91}
{"curie": "UMLS:C4525659", "names": ["Stage IV Jejunal Neuroendocrine Tumor", "Stage IV Jejunal Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Jejunal Neuroendocrine Tumor AJCC v8", "shortest_name_length": 37}
{"curie": "MONDO:0020632", "names": ["DEE93", "IECEE3", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 93", "developmental and epileptic encephalopathy 93", "infantile or early childhood epileptic encephalopathy 3", "epileptic encephalopathy, infantile or early childhood, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epileptic encephalopathy, infantile or early childhood, 3", "shortest_name_length": 5}
{"curie": "UMLS:C1704453", "names": ["Sinonasal Oncocytic Papilloma", "Oncocytic Schneiderian papilloma", "Oncocytic Schneiderian Papilloma", "Sinonasal Oncocytic Schneiderian Papilloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Oncocytic Papilloma", "shortest_name_length": 29}
{"curie": "MONDO:0000941", "names": ["eyelid degeneration", "degeneration of eyelid", "Eyelid degenerative disorder", "eyelid degenerative disorder", "Degenerative disorder of eyelid", "eyelid neurodegenerative disease", "degeneration of eyelid (diagnosis)", "neurodegenerative disease of eyelid", "Degenerative disorder of eyelid, NOS", "Degenerative disorder of eyelid (disorder)", "Degenerative disorder of eyelid, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eyelid degenerative disorder", "shortest_name_length": 19}
{"curie": "MONDO:0013254", "names": ["MCSZ", "DEE10", "EIEE10", "early infantile epileptic encephalopathy 10", "early infantile epileptic encephalopathy-10", "epileptic encephalopathy, early infantile, 10", "developmental and epileptic encephalopathy 10", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 10", "microcephaly - seizures - developmental delay", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 10", "microcephaly, seizures, and developmental delay", "MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly, seizures, and developmental delay", "shortest_name_length": 4}
{"curie": "MONDO:0007667", "names": ["subependymoma", "SUBEPENDYMOMA", "Subependymoma", "Subependymomas", "subependymal glioma", "Subependymal Glioma", "Subependymal glioma", "Subependymal Gliomas", "Glioma, Subependymal", "SUBEPENDYMOMA, benign", "Gliomas, Subependymal", "SUBEPENDYMOMA, BENIGN", "Subependymal astrocytoma", "Subependymal Astrocytoma", "subependymal astrocytoma", "astrocytoma subependymal", "astrocytoma; subependymal", "subependymal; astrocytoma", "Subependymal Astrocytomas", "Astrocytoma, Subependymal", "Astrocytomas, Subependymal", "Who Grade I Ependymal Tumor", "WHO grade I Ependymal tumor", "WHO Grade I Ependymal Tumor", "WHO grade I ependymal tumor", "WHO Grade 1 Ependymal Tumor", "Subependymal astrocytoma, NOS", "mixed subependymoma-ependymoma", "WHO Grade 1 Ependymal Neoplasm", "Mixed subependymoma-ependymoma", "WHO grade I ependymal neoplasm", "WHO Grade I Ependymal Neoplasm", "Who Grade I Ependymal Neoplasm", "subependymal astrocytoma (formerly)", "Subependymal glioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subependymoma", "shortest_name_length": 13}
{"curie": "UMLS:C0014347", "names": ["Enterobacterial Infection", "Enterobacteriaceae disease", "Infection, Enterobacterial", "Enterobacterial Infections", "Infections, Enterobacterial", "Enterobacteriaceae Infection", "Infection, Enterobacteriaceae", "Enterobacteriaceae Infections", "Infections, Enterobacteriaceae", "Infection due to Enterobacteriaceae", "Infection caused by Enterobacteriaceae", "Infection caused by Enterobacteriaceae (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Enterobacteriaceae Infections", "shortest_name_length": 25}
{"curie": "UMLS:C0398368", "names": ["Lymphatic Abnormality", "lymphatic abnormality", "Abnormality, Lymphatic", "lymphatic malformation", "Lymphatic malformation", "Lymphatic malformations", "Lymphatic Abnormalities", "lymphatic malformations", "Abnormalities, Lymphatic", "Lymphatics--Abnormalities", "Lymphatic malformation (disorder)", "Lymphatic malformation (diagnosis)", "disorder of lymphatic vessel lymphatic malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphatic Abnormalities", "shortest_name_length": 21}
{"curie": "MONDO:0006339", "names": ["MCST", "microcystic stromal tumor", "ovarian microcystic stromal tumor", "Ovarian Microcystic Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian microcystic stromal tumor", "shortest_name_length": 4}
{"curie": "MONDO:0017724", "names": ["hexosaminidase A deficiency, infantile form", "Tay-Sachs disease, b variant, infantile form", "GM2 gangliosidosis, B variant, infantile form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tay-Sachs disease, b variant, infantile form", "shortest_name_length": 43}
{"curie": "UMLS:C2987503", "names": ["stage III gallbladder cancer", "Stage III Gallbladder Cancer", "Stage III Gallbladder Cancer AJCC v7", "Stage III Gallbladder Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Gallbladder Cancer AJCC v7", "shortest_name_length": 28}
{"curie": "UMLS:C0009178", "names": ["Cocaine withdrawal", "withdrawal cocaine", "COCAINE WITHDRAWAL", "cocaine withdrawal", "cocaine withdrawals", "Cocaine withdrawal syndrome", "cocaine withdrawal (diagnosis)", "Cocaine withdrawal syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cocaine withdrawal", "shortest_name_length": 18}
{"curie": "UMLS:C5670684", "names": ["Stage IVB Cervical Cancer FIGO 2009", "Stage IVB Cervical Carcinoma FIGO 2009"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Cervical Cancer FIGO 2009", "shortest_name_length": 35}
{"curie": "MONDO:0024332", "names": ["atopic rhinitis", "allergic rhinitis perennial", "Perennial Allergic Rhinitis", "Perennial allergic rhinitis", "perennial allergic rhinitis", "Rhinitis, Allergic, Perennial", "Nonseasonal allergic rhinitis", "nonseasonal allergic rhinitis", "Non-seasonal Allergic Rhinitis", "non-seasonal allergic rhinitis", "Non-seasonal allergic rhinitis", "allergic; rhinitis, nonseasonal", "rhinitis; allergic, nonseasonal", "Rhinitis, Allergic, Nonseasonal", "Perennial allergic rhinitis (disorder)", "Perennial allergic rhinitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "perennial allergic rhinitis", "shortest_name_length": 15}
{"curie": "MONDO:0010414", "names": ["RBMX1A", "Myopathy, Reducing Body, X-Linked, Early-Onset, Severe", "myopathy, reducing body, X-linked, early-onset, severe", "reducing body myopathy, X-linked 1A, severe, with infantile or early childhood onset", "REDUCING BODY MYOPATHY, X-LINKED 1A, SEVERE, WITH INFANTILE OR EARLY CHILDHOOD ONSET", "reducing body myopathy, X-linked 1a, severe, infantile or early childhood onset, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy, reducing body, X-linked, early-onset, severe", "shortest_name_length": 6}
{"curie": "UMLS:C4330696", "names": ["SCHAD Hyperinsulinism", "HADH-Associated Hyperinsulinism", "Mitochondrial Hydroxyacyl-Coenzyme A Dehydrogenase Hyperinsulinism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mitochondrial Hydroxyacyl-Coenzyme A Dehydrogenase Hyperinsulinism", "shortest_name_length": 21}
{"curie": "UMLS:C1707548", "names": ["Cutaneous Hematopoietic and Lymphoid Cell Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous Hematopoietic and Lymphoid Cell Neoplasm", "shortest_name_length": 50}
{"curie": "MONDO:0012743", "names": ["BRGDA4", "Brugada syndrome 4", "Brugada Syndrome 4", "BRUGADA SYNDROME 4", "CACNB2 Brugada syndrome", "Brugada syndrome type 4", "Brugada syndrome 4 (diagnosis)", "Brugada syndrome caused by mutation in CACNB2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brugada syndrome 4", "shortest_name_length": 6}
{"curie": "MONDO:0008108", "names": ["OCCS", "OCC syndrome", "Delleman syndrome", "DELLEMAN SYNDROME", "Delleman Oorthuys syndrome", "Delleman-Oorthuys syndrome", "Leichtman-Wood-Rohn syndrome", "OCULOCEREBROCUTANEOUS SYNDROME", "oculocerebrocutaneous syndrome", "Oculocerebrocutaneous syndrome", "Oculo-cerebro-cutaneous syndrome", "oculo-cerebro-cutaneous syndrome", "oculo-cerebro-cutaneous (OCC) syndrome", "Oculocerebrocutaneous syndrome (disorder)", "ORBITAL CYST WITH CEREBRAL AND FOCAL DERMAL MALFORMATIONS", "Orbital cyst with cerebral and focal dermal malformations", "orbital cyst with cerebral and focal dermal malformations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculocerebrocutaneous syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0035521", "names": ["BPES plus", "3q23 microdeletion syndrome", "blepharophimosis-ptosis-epicanthus inversus syndrome plus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blepharophimosis-ptosis-epicanthus inversus syndrome plus", "shortest_name_length": 9}
{"curie": "UMLS:C4289600", "names": ["Early Prosthetic Valve Endocarditis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Early Prosthetic Valve Endocarditis", "shortest_name_length": 35}
{"curie": "MONDO:0019672", "names": ["fibular hemimelia", "fibular longitudinal meromelia", "congenital longitudinal deficiency of the fibula"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibular hemimelia", "shortest_name_length": 17}
{"curie": "MONDO:0002428", "names": ["Protozoosis", "Protozoiasis", "Protozoosis, NOS", "Protozoal disease", "Protozoiasis, NOS", "protozoal disease", "protozoal; disease", "protozoal diseases", "Protozoal diseases", "disease; protozoal", "Protozoan infection", "Infection protozoal", "INFECTION PROTOZOAL", "protozoan infection", "Protozoal Infection", "protozoal infection", "Protozoan Infection", "protozoal; infection", "protozoan infections", "Protozoan Infections", "Infection, Protozoan", "infection; protozoal", "infections protozoal", "protozoal infestation", "Infections, Protozoan", "protozoal; infestation", "infestation; protozoal", "Protozoal infection NOS", "protozoa infectious disease", "Protozoal diseases (B50-B64)", "Unspecified protozoal disease", "protozoal disease (diagnosis)", "PROTOZOAL INFECTIOUS DISEASES", "Protozoal infectious disorders", "Protozoan infection (disorder)", "mastigophora infectious disease", "Mastigophora infectious disease", "sarcomastigophora infectious disease", "parasitic protozoa infectious disease", "disease (or disorder); protozoal, protozoal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "protozoa infectious disease", "shortest_name_length": 11}
{"curie": "UMLS:C5237457", "names": ["T-MF", "Transformed Mycosis Fungoides"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transformed Mycosis Fungoides", "shortest_name_length": 4}
{"curie": "UMLS:C0677699", "names": ["Stage II Non-Hodgkin Lymphoma", "noncontiguous stage II adult non-Hodgkin lymphoma", "Stage II Non-Contiguous Adult Non-Hodgkin Lymphoma", "stage II non-contiguous adult non-Hodgkin lymphoma", "stage II adult noncontiguous non-Hodgkin's lymphoma", "adult noncontiguous non-Hodgkin's lymphoma stage II", "Stage II Adult NonContiguous Non-Hodgkin's Lymphoma", "Adult NonContiguous Non-Hodgkin's Lymphoma Stage II", "Stage II Adult Non-Contiguous Non-Hodgkin's Lymphoma", "adult non-contiguous stage II non-Hodgkin's lymphoma", "non-contiguous stage II adult non-Hodgkin's lymphoma", "non-contiguous adult non-Hodgkin's lymphoma stage II", "stage II non-contiguous adult non-Hodgkin's lymphoma", "Non-Contiguous Adult Non-Hodgkin's Lymphoma Stage II", "adult non-contiguous non-Hodgkin's lymphoma stage II", "Non-Contiguous Stage II Adult Non-Hodgkin's Lymphoma", "Adult Non-Contiguous Stage II Non-Hodgkin's Lymphoma", "Stage II Non-Contiguous Adult Non-Hodgkin's Lymphoma", "Adult Non-Contiguous Non-Hodgkin's Lymphoma Stage II", "stage II adult non-contiguous non-Hodgkin's lymphoma", "Ann Arbor Stage II Non-Contiguous Adult Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage II Non-Contiguous Adult Non-Hodgkin Lymphoma", "shortest_name_length": 29}
{"curie": "MONDO:0013855", "names": ["susceptibility to severe influenza", "INFLUENZA, SEVERE, SUSCEPTIBILITY TO", "influenza, severe, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "influenza, severe, susceptibility to", "shortest_name_length": 34}
{"curie": "UMLS:C1708881", "names": ["Malignant Hair Follicle Tumor", "Malignant Hair Follicle Neoplasm", "HAIR FOLLICLE NEOPLASM, MALIGNANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Hair Follicle Neoplasm", "shortest_name_length": 29}
{"curie": "MONDO:0019310", "names": ["RDEB-I", "inverse RDEB", "dystrophic epidermolysis bullosa inversa", "recessive dystrophic epidermolysis bullosa inversa", "inverse recessive dystrophic epidermolysis bullosa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "recessive dystrophic epidermolysis bullosa inversa", "shortest_name_length": 6}
{"curie": "UMLS:C4528560", "names": ["Stage IIIC Breast Cancer", "stage IIIC breast cancer", "anatomic stage IIIC breast cancer", "anatomic stage IIIC breast carcinoma", "Anatomic Stage IIIC Breast Cancer AJCC v8", "Anatomic Stage IIIC Breast Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anatomic Stage IIIC Breast Cancer AJCC v8", "shortest_name_length": 24}
{"curie": "UMLS:C5446657", "names": ["TCCRP", "Breast Tall Cell Carcinoma with Reversed Polarity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Tall Cell Carcinoma with Reversed Polarity", "shortest_name_length": 5}
{"curie": "UMLS:C0457798", "names": ["eyelid eczema", "Eyelid eczema", "eczema eyelid", "Eczema of eyelid", "dermatitis eyelid", "Dermatitis;eyelid", "Dermatitis eyelid", "DERMATITIS EYELID", "eyelid dermatitis", "dermatitis of eyelid", "Dermatitis of eyelid", "Dermatitis of eyelid, NOS", "Dermatitis of eyelid (disorder)", "dermatitis of eyelid (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dermatitis of eyelid", "shortest_name_length": 13}
{"curie": "MONDO:0017185", "names": ["Dominant KATP hyperinsulinism due to Kir6.2 deficiency", "dominant KATP hyperinsulinism due to Kir6.2 deficiency", "Autosomal dominant hyperinsulinism due to Kir6.2 deficiency", "autosomal dominant hyperinsulinism due to Kir6.2 deficiency", "Autosomal dominant hyperinsulinism due to Kir6.2 deficiency (disorder)", "Autosomal dominant hyperinsulinemic hypoglycemia due to Kir6.2 deficiency", "autosomal dominant hyperinsulinemic hypoglycemia due to Kir6.2 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant hyperinsulinism due to Kir6.2 deficiency", "shortest_name_length": 54}
{"curie": "MONDO:0011404", "names": ["Car", "CAR", "Caronte", "CARONTE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Caronte", "shortest_name_length": 3}
{"curie": "MONDO:0007979", "names": ["METCDS", "METACHONDROMATOSIS", "Metachondromatosis", "metachondromatosis", "Metachondromatosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metachondromatosis", "shortest_name_length": 6}
{"curie": "UMLS:C1535948", "names": ["Retinal aneurysm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retinal aneurysm", "shortest_name_length": 16}
{"curie": "MONDO:0100290", "names": ["Colon Serrated Polyposis", "colon serrated polyposis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colon serrated polyposis", "shortest_name_length": 24}
{"curie": "UMLS:C5554632", "names": ["WHO Grade 1 Glioma", "WHO Grade I Glioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "WHO Grade 1 Glioma", "shortest_name_length": 18}
{"curie": "UMLS:C0278690", "names": ["Recurrent Brain Neoplasm", "recurrent childhood CNS tumor", "recurrent pediatric CNS tumor", "Relapsed Childhood Brain Tumor", "Relapsed Pediatric Brain Tumor", "pediatric CNS tumor, recurrent", "CNS tumor, recurrent childhood", "childhood CNS tumor, recurrent", "Recurrent Pediatric Brain Tumor", "Recurrent Childhood Brain Tumor", "recurrent, CNS tumor, childhood", "CNS tumor, childhood, recurrent", "CNS tumor, pediatric, recurrent", "recurrent childhood brain tumor", "recurrent pediatric brain tumor", "recurrent brain tumor, childhood", "childhood brain tumor, recurrent", "pediatric brain tumor, recurrent", "brain tumor, childhood, recurrent", "brain tumor, pediatric, recurrent", "Relapsed Tumor of Pediatric Brain", "Relapsed Pediatric Brain Neoplasm", "Relapsed Tumor of Childhood Brain", "Relapsed Childhood Brain Neoplasm", "brain tumor, recurrent, childhood", "Recurrent Tumor of Pediatric Brain", "Recurrent Tumor of Childhood Brain", "Recurrent Childhood Brain Neoplasm", "Recurrent Pediatric Brain Neoplasm", "Relapsed Neoplasm of Childhood Brain", "Relapsed Neoplasm of Pediatric Brain", "Relapsed Tumor of the Childhood Brain", "Relapsed Tumor of the Pediatric Brain", "Recurrent Neoplasm of Childhood Brain", "Recurrent Neoplasm of Pediatric Brain", "Recurrent Tumor of the Pediatric Brain", "Recurrent Tumor of the Childhood Brain", "Relapsed Neoplasm of the Childhood Brain", "Relapsed Neoplasm of the Pediatric Brain", "Recurrent Neoplasm of the Pediatric Brain", "Recurrent Neoplasm of the Childhood Brain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Brain Neoplasm", "shortest_name_length": 24}
{"curie": "UMLS:C0153789", "names": ["Stage II Subdiaphragmatic Hodgkin Lymphoma", "Stage II Subdiaphragmatic Hodgkin's Disease", "Stage II Subdiaphragmatic Hodgkin's Lymphoma", "Stage II Hodgkin's Disease below the Diaphragm", "Stage II Hodgkin's Lymphoma below the Diaphragm", "Hodgkin lymphoma of inguinal region or lower limb", "Ann Arbor Stage II Subdiaphragmatic Hodgkin Lymphoma", "Hodgkin's disease NOS stage II subdiaphragmatic presentation", "Hodgkin lymphoma of inguinal region or lower limb (diagnosis)", "Hodgkin's disease, NOS of lymph nodes of inguinal region and lower limb", "Hodgkin's disease, unspecified type, lymph nodes of inguinal region and lower limb", "Hodgkin's disease, unspecified type, involving lymph nodes of inguinal region and lower limb"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's disease NOS stage II subdiaphragmatic presentation", "shortest_name_length": 42}
{"curie": "MONDO:0005231", "names": ["HCV", "NANBH", "PT-NANBH", "hepatitis c", "Hepatitis C", "HEPATITIS C", "hepatitis C", "HCV Infection", "non b hepatitis", "Hep non-A non-B", "hepatitis type C", "hepatitis c viral", "viral hepatitis c", "viral hepatitis C", "Viral hepatitis C", "HEPATITIS C VIRUS", "hepatitis viral c", "nonA nonB hepatitis", "chronic hepatitis C", "hepatitis nonA nonB", "hepatitis Nona nonB", "Non-A non-B hepatitis", "Hepatitis non-A non-B", "non-A non-B-hepatitis", "hepatitis non-a non-b", "hepatitis non A non B", "hepatitis C infection", "Viral hepatitis C NOS", "HEPATITIS NON-A NON-B", "Hepatitis C Infection", "HEPATITIS NON A NON B", "Non-A, non-B hepatitis", "Type C viral hepatitis", "non-A, non-B Hepatitis", "Viral hepatitis type C", "Non-A, Non-B Hepatitis", "Hepatitis (non-A non-B)", "Hepatitis, Non-A, non-B", "Hepatitis C virus (HCV)", "HEPATITIS, NON-A, NON-B", "hepatitis; virus, type C", "Hepatitis C Virus Infection", "hepatitis viral non-A non-B", "hepatitis C virus infection", "viral hepatitis C infection", "Hepatitis C virus hepatitis", "Viral hepatitis, non-A, non-B", "Unspecified viral hepatitis C", "viral hepatitis C (diagnosis)", "hepatitis; virus, non-A, non-B", "virus; hepatitis, non-A, non-B", "Unspecified viral hepatitis C NOS", "Viral hepatitis type C (disorder)", "Hepatitis non-A non-B (diagnosis)", "Hepatitis C virus caused hepatitis", "Parenterally Transmitted Non A, Non B Hepatitis", "Parenterally-Transmitted Non-A, Non-B Hepatitis", "Hepatitis, Viral, Non-A, Non-B, Parenterally-Transmitted"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatitis C virus infection", "shortest_name_length": 3}
{"curie": "UMLS:C5446877", "names": ["Breast Classic LCIS", "Breast Classic Lobular Carcinoma In Situ"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Classic Lobular Carcinoma In Situ", "shortest_name_length": 19}
{"curie": "UMLS:C4521628", "names": ["Stage IVB Sinonasal Cancer AJCC v8", "Stage IVB Sinonasal Carcinoma AJCC v8", "Stage IVB Nasal Cavity and Paranasal Sinus Cancer", "Stage IVB Nasal Cavity and Paranasal Sinus Cancer AJCC v8", "Stage IVB Nasal Cavity and Paranasal Sinus Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Nasal Cavity and Paranasal Sinus Cancer AJCC v8", "shortest_name_length": 34}
{"curie": "UMLS:C4525406", "names": ["Recurrent Ph-Like Acute Lymphoblastic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Ph-Like Acute Lymphoblastic Leukemia", "shortest_name_length": 46}
{"curie": "UMLS:C2348874", "names": ["BilIN-2", "Biliary Intraepithelial Neoplasia-2", "Grade 2 Biliary Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Biliary Intraepithelial Neoplasia-2", "shortest_name_length": 7}
{"curie": "MONDO:0000525", "names": ["cecum adenoma", "caecum adenoma", "Cecum Villous Adenoma", "Cecal Villous Adenoma", "cecum villous adenoma", "cecal villous adenoma", "caecum villous adenoma", "villous adenoma of cecum", "Villous Adenoma of Cecum", "villous adenoma of the cecum", "Villous Adenoma of the Cecum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cecum villous adenoma", "shortest_name_length": 13}
{"curie": "MONDO:0015237", "names": ["Arhinia", "arrhinia", "Arrhinia", "Absent nose", "nose; absent", "Missing nose", "Nose agenesia", "Nose agenesis", "nose; atresia", "absence; nose", "atresia; nose", "agenesis; nose", "nose; agenesis", "Agenesis of nose", "Isolated arrhinia", "isolated arrhinia", "Aplasia of the nose", "Isolated nose agenesis", "isolated nose agenesis", "Nasal underdevelopment", "Underdevelopment of nose", "Congenital absence of nose", "arrhinia (physical finding)", "Failure of development of nose", "Congenital absence of the nose", "congenital absence of the nose", "Congenital absence of nose (disorder)", "Agenesis and underdevelopment of nose"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arrhinia", "shortest_name_length": 7}
{"curie": "MONDO:0022580", "names": ["blepharo naso facial syndrome van Maldergem type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blepharo naso facial syndrome van Maldergem type", "shortest_name_length": 48}
{"curie": "MONDO:0010379", "names": ["BRNRS", "Brunner Syndrome", "BRUNNER SYNDROME", "Brunner syndrome", "brunner syndrome", "monoamine oxidase deficiency", "monoamine oxidase A deficiency", "Monoamine oxidase A deficiency", "Deficiency of monoamine oxidase A", "Brunner syndrome, X-linked recessive", "X-linked monoamine oxidase deficiency", "monoamine oxidase A (MAOA) deficiency", "ANTISOCIAL BEHAVIOR, SUSCEPTIBILITY TO", "antisocial behavior, susceptibility to", "antisocial behavior, X-linked recessive", "Deficiency of monoamine oxidase A (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brunner syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C5447600", "names": ["Metastatic Nasopharyngeal Nonkeratinizing Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Nasopharyngeal Nonkeratinizing Carcinoma", "shortest_name_length": 51}
{"curie": "MONDO:0002922", "names": ["PYODERMA", "Pyoderma", "pyoderma", "pyodermia", "Pyodermia", "Pyodermas", "Pustuloderma", "pyodermatitis", "septic dermatitis", "Septic dermatitis", "Pus-filled lesion", "Dermatitis, septic", "Purulent dermatitis", "Pyoderma (disorder)", "Dermatitis pyogenic", "Pyogenic dermatitis", "DERMATITIS PYOGENIC", "Dermatitis, purulent", "pyoderma (diagnosis)", "Pyoderma, unspecified", "suppurative dermatitis", "Suppurative dermatitis", "Dermatitis, suppurative", "skin; lesion, suppurative", "Pyoderma (skin infection)", "PYODERMA (SKIN INFECTION)", "lesion; skin, suppurative", "Pyogenic infection of skin and subcutis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyoderma", "shortest_name_length": 8}
{"curie": "UMLS:C4087006", "names": ["Childhood Intermixed Ganglioneuroblastoma", "Childhood Ganglioneuroblastoma, Intermixed"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Ganglioneuroblastoma, Intermixed", "shortest_name_length": 41}
{"curie": "MONDO:0010024", "names": ["SRPS4", "Srps 4", "SRTD12", "SRPS IV", "SRPS type 4", "SRPS, type 4", "Beemer Langer syndrome", "Beemer-Langer syndrome", "BEEMER-LANGER SYNDROME", "Beemer-Langer Syndrome", "short rib syndrome, Beemer type", "short-rib thoracic dysplasia 12", "SHORT RIB SYNDROME, BEEMER TYPE", "Short Rib Syndrome, Beemer Type", "SHORT-RIB THORACIC DYSPLASIA 12", "short rib-polydactyly syndrome type 4", "Short rib-polydactyly syndrome type 4", "type IV short rib polydactyly syndrome", "short rib-polydactyly syndrome type IV", "Type IV short rib polydactyly syndrome", "short rib-polydactyly syndrome, type 4", "Short rib-polydactyly syndrome, type 4", "SHORT RIB-POLYDACTYLY SYNDROME, TYPE IV", "Short Rib-Polydactyly Syndrome, Type IV", "short rib-polydactyly syndrome Beemer type", "Short rib-polydactyly syndrome, Beemer type", "Type IV short rib polydactyly syndrome (disorder)", "Beemer-Langer type short rib polydactyly syndrome", "short rib polydactyly syndrome Beemer-Langer type", "Short rib-polydactyly syndrome, Beemer-Langer type", "short rib-polydactyly syndrome, Beemer-Langer type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Beemer-Langer syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0009775", "names": ["CSNBO1", "Oguchi Disease 1", "OGUCHI DISEASE 1", "Oguchi disease 1", "Oguchi disease-1", "SAG Oguchi disease", "Oguchi disease type 1", "Oguchi disease caused by mutation in SAG", "congenital stationary night blindness Oguchi type 1", "night blindness, congenital stationary, Oguchi type 1", "NIGHT BLINDNESS, CONGENITAL STATIONARY, OGUCHI TYPE 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oguchi disease-1", "shortest_name_length": 6}
{"curie": "UMLS:C0751071", "names": ["Familial Dementia", "Familial Dementias", "Dementia, Familial", "Dementias, Familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Familial Dementia", "shortest_name_length": 17}
{"curie": "UMLS:C1709153", "names": ["Differentiated Nasopharyngeal Cancer", "Nasopharyngeal Differentiated Carcinoma", "Nasopharyngeal Nonkeratinizing Differentiated Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasopharyngeal Differentiated Carcinoma", "shortest_name_length": 36}
{"curie": "MONDO:0008184", "names": ["pancreas agenesis, dorsal", "Pancreas agenesis, dorsal", "congenital short pancreas", "Pancreas, dorsal, agenesis of", "PANCREAS, DORSAL, AGENESIS OF", "pancreas, dorsal, agenesis of", "Agenesis of the dorsal pancreas", "agenesis of the dorsal pancreas", "partial agenesis of the dorsal pancreas", "complete agenesis of the dorsal pancreas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreas, dorsal, agenesis of", "shortest_name_length": 25}
{"curie": "UMLS:C0855013", "names": ["Relapsed Chondrosarcoma", "Recurrent Chondrosarcoma", "Chondrosarcoma recurrent", "Chondrosarcoma, Recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chondrosarcoma recurrent", "shortest_name_length": 23}
{"curie": "UMLS:C1332538", "names": ["Benign Skeletal Muscle Tumor", "Benign Skeletal Muscle Neoplasm", "Benign Tumor of Skeletal Muscle", "Benign Neoplasm of Skeletal Muscle", "Benign Tumor of the Skeletal Muscle", "Benign Neoplasm of the Skeletal Muscle"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Skeletal Muscle Neoplasm", "shortest_name_length": 28}
{"curie": "MONDO:0019197", "names": ["folinic acid-responsive seizures", "Folinic acid-responsive seizures", "Folinic acid responsive seizures", "Folinic acid responsive seizure syndrome", "Folinic acid responsive seizure syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "folinic acid-responsive seizures", "shortest_name_length": 32}
{"curie": "UMLS:C0221255", "names": ["Metastatic calcification", "METASTATIC CALCIFICATION", "CALCIFICATION METASTATIC", "Calcification metastatic", "Calcification, metastatic", "calcification; metastatic", "metastatic; calcification", "Metastatic calcification (disorder)", "Metastatic calcification, calcified structure", "Metastatic calcification, calcified structure (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic calcification", "shortest_name_length": 24}
{"curie": "EFO:1000656", "names": ["sporadic Creutzfeld Jacob disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sporadic Creutzfeld Jacob disease", "shortest_name_length": 33}
{"curie": "MONDO:0003664", "names": ["hemolytic anemia", "Anemia hemolytic", "Hemolytic anemia", "anemia hemolytic", "Hemolytic Anemia", "HEMOLYTIC ANEMIA", "ANEMIA HEMOLYTIC", "Hemolytic anaemia", "Anemia, Hemolytic", "hemolytic anemias", "anemia, hemolytic", "hemolytic; anemia", "Hemolytic anemias", "anemia; hemolytic", "Anaemia;haemolytic", "Haemolytic Anaemia", "haemolytic anaemia", "Haemolytic anaemia", "Anaemia haemolytic", "ANAEMIA HAEMOLYTIC", "haemolytic anaemias", "Anaemia, Haemolytic", "Haemolytic Anaemias", "Increased hemolysis", "Haemolytic anaemias", "Hemolytic anemia NOS", "Hemolytic anemia, NOS", "Anemia hemolytic (NOS)", "Haemolytic anaemia NOS", "Hemolytic anemia (NOS)", "HEMOLYTIC ANEMIA (NOS)", "ANEMIA HEMOLYTIC (NOS)", "Haemolytic anaemia, NOS", "Hemolytic anemia (disorder)", "Hemolytic anemias (D55-D59)", "hemolytic anemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemolytic anemia", "shortest_name_length": 16}
{"curie": "UMLS:C4086151", "names": ["Anaplastic Ependymoma", "Childhood Anaplastic Ependymoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Anaplastic Ependymoma", "shortest_name_length": 21}
{"curie": "MONDO:0011433", "names": ["anemia, congenital hypoplastic, with multiple congenital anomalies/mental retardation syndrome", "Anemia, Congenital Hypoplastic, with Multiple Congenital Anomalies-Mental Retardation Syndrome", "ANEMIA, CONGENITAL HYPOPLASTIC, WITH MULTIPLE CONGENITAL ANOMALIES/MENTAL RETARDATION SYNDROME", "anemia, congenital hypoplastic, with multiple congenital anomalies/intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anemia, congenital hypoplastic, with multiple congenital anomalies/intellectual disability syndrome", "shortest_name_length": 94}
{"curie": "UMLS:C1333604", "names": ["Female Reproductive System Precancerous Condition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Female Reproductive System Precancerous Condition", "shortest_name_length": 49}
{"curie": "MONDO:0003680", "names": ["Periosteal Chondrosarcoma", "Periosteal chondrosarcoma", "periosteal chondrosarcoma", "Juxtacortical chondrosarcoma", "Juxtacortical Chondrosarcoma", "juxtacortical chondrosarcoma", "periosteum chondrosarcoma (disease)", "chondrosarcoma (disease) of periosteum", "juxtacortical chondrosarcoma (morphologic abnormality)", "Juxtacortical chondrosarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "periosteal chondrosarcoma", "shortest_name_length": 25}
{"curie": "MONDO:0009971", "names": ["RDS", "IRDS", "NRDS", "RDS - infants", "RDS Of Prematurity", "RDS OF PREMATURITY", "RDS of prematurity", "hyaline Membrane disease", "respiratory distress syndrome", "hyaline Membrane disease, formerly", "HYALINE MEMBRANE DISEASE, FORMERLY", "respiratory distress syndrome, infant", "infantile respiratory distress syndrome", "respiratory distress syndrome in premature infants", "RESPIRATORY DISTRESS SYNDROME IN PREMATURE INFANTS", "Respiratory Distress Syndrome In Premature Infants"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "respiratory distress syndrome in premature infants", "shortest_name_length": 3}
{"curie": "UMLS:C0521624", "names": ["Ectopic renin secretion", "Ectopic Renin Secretion", "Ectopic Renin Secretion Syndrome", "Ectopic renin secretion (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ectopic renin secretion", "shortest_name_length": 23}
{"curie": "UMLS:C2828028", "names": ["Stage IA Skin Melanoma AJCC v7", "Stage IA Cutaneous (Skin) Melanoma", "Stage IA Cutaneous Melanoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Cutaneous Melanoma AJCC v7", "shortest_name_length": 30}
{"curie": "UMLS:C1336260", "names": ["Stage III Osteosarcoma", "Stage III Osteogenic Sarcoma", "Stage III Osteosarcoma AJCC v7", "Stage III Osteosarcoma  AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Osteosarcoma AJCC v7", "shortest_name_length": 22}
{"curie": "MONDO:0008790", "names": ["anemia, nonspherocytic hemolytic, possibly due to defect in porphyrin metabolism", "Anemia, Nonspherocytic Hemolytic, possibly due to Defect in Porphyrin Metabolism", "ANEMIA, NONSPHEROCYTIC HEMOLYTIC, POSSIBLY DUE TO DEFECT IN PORPHYRIN METABOLISM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anemia, nonspherocytic hemolytic, possibly due to defect in porphyrin metabolism", "shortest_name_length": 80}
{"curie": "UMLS:C4087096", "names": ["Childhood Myxopapillary Ependymoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Myxopapillary Ependymoma", "shortest_name_length": 34}
{"curie": "UMLS:C1336408", "names": ["Paranasal Sinus Cancer Stage IVC", "Stage IVC Paranasal Sinus Cancer", "Stage IVC Accessory Sinus Carcinoma", "Stage IVC Paranasal Sinus Carcinoma", "Stage IVC Carcinoma of Accessory Sinus", "Stage IVC Carcinoma of Paranasal Sinus", "Stage IVC Paranasal Sinus Cancer AJCC v7", "Stage IVC Carcinoma of the Accessory Sinus", "Stage IVC Carcinoma of the Paranasal Sinus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Paranasal Sinus Cancer AJCC v7", "shortest_name_length": 32}
{"curie": "UMLS:C1332069", "names": ["AJCC G4 Sarcoma", "AJCC Grade 4 Sarcoma", "AJCC Grade IV Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AJCC Grade 4 Sarcoma", "shortest_name_length": 15}
{"curie": "UMLS:C0273483", "names": ["CRANIAL NERVE INJURY", "cranial nerve injury", "Cranial nerve injury", "Cranial Nerve Injury", "Injury, Cranial Nerve", "Nerve Injury, Cranial", "Cranial nerve injuries", "Cranial Nerve Injuries", "cranial nerve injuries", "Injuries, Cranial Nerve", "injury to cranial nerve", "Nerve Injuries, Cranial", "Injury of cranial nerve", "Injury of cranial nerves", "Cranial nerve injury NOS", "Traumatic Cranial Neuropathy", "Injury of cranial nerve, NOS", "Cranial Neuropathy, Traumatic", "Neuropathy, Traumatic Cranial", "injury to other cranial nerve", "injury to the cranial nerve(s)", "traumatic cranial nerve injury", "Traumatic Cranial Neuropathies", "Neuropathies, Traumatic Cranial", "Cranial Neuropathies, Traumatic", "cranial nerve injury (diagnosis)", "Injury of cranial nerve (disorder)", "injury to cranial nerve (diagnosis)", "Injury to unspecified cranial nerve", "Injury of unspecified cranial nerve", "traumatic cranial nerve injury (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cranial Nerve Injuries", "shortest_name_length": 20}
{"curie": "UMLS:C0151899", "names": ["Screaming syndrome", "Syndrome screaming", "SYNDROME SCREAMING", "SCREAMING SYNDROME", "CRYING DPT VACCINE RELATED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Screaming syndrome", "shortest_name_length": 18}
{"curie": "MONDO:0022013", "names": ["Boerhave syndrome", "boerhaave syndrome", "BOERHAAVE SYNDROME", "Boerhaave syndrome", "boerhaaves syndrome", "Boerhaave's syndrome", "boerhaave's syndrome", "BOERHAAVE'S SYNDROME", "Spontaneous esophageal rupture", "spontaneous rupture of esophagus", "Spontaneous rupture of esophagus", "Boerhaave's syndrome (diagnosis)", "Spontaneous rupture of oesophagus", "Spontaneous esophageal perforation", "spontaneous esophageal perforation", "Spontaneous oesophageal perforation", "spontaneous perforation of esophagus", "Spontaneous perforation of esophagus", "spontaneous rupture of the esophagus", "Spontaneous perforation of oesophagus", "spontaneous perforation of the esophagus", "Spontaneous rupture of esophagus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Boerhaave syndrome", "shortest_name_length": 17}
{"curie": "MONDO:0044747", "names": ["Anaplasmosis", "anaplasmoses", "anaplasmosis", "human anaplasmosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "human anaplasmosis", "shortest_name_length": 12}
{"curie": "MONDO:0013338", "names": ["CMTRIB", "RI-CMTB", "RI-CMT type B", "KARS Charcot-Marie-Tooth disease", "Charcot-Marie-Tooth disease recessive intermediate B", "CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE B", "Charcot-Marie-Tooth disease, recessive intermediate B", "Charcot-Marie-Tooth disease, recessive intermediate, B", "Charcot-Marie-Tooth disease caused by mutation in KARS", "Charcot-Marie-Tooth neuropathy recessive intermediate B", "Charcot-Marie-Tooth neuropathy, recessive Intermediate B", "CHARCOT-MARIE-TOOTH NEUROPATHY, RECESSIVE INTERMEDIATE B", "Charcot-Marie-Tooth disease recessive intermediate type B", "Charcot-Marie-Tooth disease, recessive Intermediate type B", "autosomal recessive intermediate Charcot-Marie-Tooth disease type B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease recessive intermediate B", "shortest_name_length": 6}
{"curie": "MONDO:0054861", "names": ["MRT63", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 63", "mental retardation, autosomal recessive 63", "intellectual disability, autosomal recessive 63", "autosomal recessive intellectual developmental disorder 63", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 63"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 63", "shortest_name_length": 5}
{"curie": "UMLS:C5420817", "names": ["Bilateral Diffuse Uveal Melanocytic Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bilateral Diffuse Uveal Melanocytic Hyperplasia", "shortest_name_length": 47}
{"curie": "MONDO:0012868", "names": ["THPH5", "Acquired protein S deficiency", "protein S acquired deficiency", "Protein S acquired deficiency", "Acquired Protein S Deficiency", "protein s deficiency acquired", "Acquired protein S deficiency (disorder)", "protein s deficiency acquired (diagnosis)", "autosomal dominant thrombophilia due to protein S deficiency", "thrombophilia due to protein S deficiency, autosomal dominant", "THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT", "thrombophilia 5 due to protein S deficiency, autosomal dominant", "autosomal dominant hereditary thrombophilia due to congenital protein S deficiency", "hereditary thrombophilia due to congenital protein S deficiency, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombophilia due to protein S deficiency, autosomal dominant", "shortest_name_length": 5}
{"curie": "MONDO:0700196", "names": ["fish melanoma", "Fish Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fish melanoma", "shortest_name_length": 13}
{"curie": "UMLS:C1334416", "names": ["Low Grade Malignant Peripheral Nerve Sheath Tumor", "Well Differentiated Malignant Peripheral Nerve Sheath Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Grade Malignant Peripheral Nerve Sheath Tumor", "shortest_name_length": 49}
{"curie": "MONDO:0030714", "names": ["OI22", "osteogenesis imperfecta, IIA 22", "OSTEOGENESIS IMPERFECTA, TYPE XXII"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteogenesis imperfecta, IIA 22", "shortest_name_length": 4}
{"curie": "UMLS:C5206454", "names": ["Stage IV Cervical Cancer FIGO 2018", "Stage IV Cervical Carcinoma FIGO 2018"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Cervical Cancer FIGO 2018", "shortest_name_length": 34}
{"curie": "MONDO:0017258", "names": ["panuveitis idiopathic", "Idiopathic panuveitis", "idiopathic panuveitis", "Idiopathic panuveitis (disorder)", "Idiopathic panuveitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic panuveitis", "shortest_name_length": 21}
{"curie": "UMLS:C1336073", "names": ["Splenic Lymphoblastic Lymphoma", "Splenic Precursor Lymphoblastic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Splenic Lymphoblastic Lymphoma", "shortest_name_length": 30}
{"curie": "UMLS:C1883531", "names": ["VMGH", "Verumontanum Mucosal Gland Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Verumontanum Mucosal Gland Hyperplasia", "shortest_name_length": 4}
{"curie": "MONDO:0012187", "names": ["FANCJ", "Fanconi anemia complementation group J", "Fanconi Anemia, Complementation Group J", "Fanconi anemia, complementation group J", "FANCONI ANEMIA, COMPLEMENTATION GROUP J", "Fanconi anemia complementation group type J", "Fanconi Anemia, complementation group type J", "Fanconi anemia complementation group J (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fanconi anemia complementation group J", "shortest_name_length": 5}
{"curie": "MONDO:0008529", "names": ["T-cell Subgroups, non-HLA-linked", "T-CELL SUBGROUPS, NON-HLA-LINKED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-cell Subgroups, non-HLA-linked", "shortest_name_length": 32}
{"curie": "MONDO:0016866", "names": ["partial deletion of chromosome 1", "partial monosomy of chromosome 1", "partial deletion of chromosome type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of chromosome 1", "shortest_name_length": 32}
{"curie": "MONDO:0003154", "names": ["nerve hemangioma", "hemangioma of nerve", "Hemangioma of Peripheral Nerve", "hemangioma of peripheral nerve"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemangioma of peripheral nerve", "shortest_name_length": 16}
{"curie": "MONDO:0000892", "names": ["colon medullary carcinoma", "Colon Medullary Carcinoma", "medullary colon carcinoma", "medullary carcinoma of the colon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colon medullary carcinoma", "shortest_name_length": 25}
{"curie": "UMLS:C4683430", "names": ["Stage II Thyroid Gland Follicular Cancer Under 55 Years", "Stage II Thyroid Gland Follicular Carcinoma Under 55 Years AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Thyroid Gland Follicular Carcinoma Under 55 Years AJCC v8", "shortest_name_length": 55}
{"curie": "MONDO:0014418", "names": ["CNM5", "centronuclear myopathy 5", "CENTRONUCLEAR MYOPATHY 5", "MYOPATHY, CENTRONUCLEAR, 5", "myopathy, centronuclear, 5", "myopathy, centronuclear, type 5", "SPEG autosomal recessive centronuclear myopathy", "autosomal recessive centronuclear myopathy caused by mutation in SPEG"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy, centronuclear, 5", "shortest_name_length": 4}
{"curie": "MONDO:0011155", "names": ["MDRV", "VACUOLAR NEUROMYOPATHY", "Vacuolar Neuromyopathy", "vacuolar Neuromyopathy", "VACUOLAR NEUROMYOPATHY (disorder)", "muscular dystrophy with rimmed vacuoles", "MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT, WITH RIMMED VACUOLES", "muscular dystrophy, autosomal dominant, with rimmed vacuoles", "Muscular Dystrophy, Autosomal Dominant, With Rimmed Vacuoles"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vacuolar Neuromyopathy", "shortest_name_length": 4}
{"curie": "UMLS:C1333089", "names": ["Colon Hodgkin Lymphoma", "Colon Hodgkin's Disease", "Colon Hodgkin's Lymphoma", "Colonic Hodgkin's Disease", "Colonic Hodgkin's Lymphoma", "Hodgkin's Lymphoma of Colon", "Hodgkin's Lymphoma of the Colon", "Primary Colon Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colon Hodgkin Lymphoma", "shortest_name_length": 22}
{"curie": "MONDO:0022430", "names": ["PPHN", "Persistent Fetal Circulation", "persistent fetal circulation", "persistent fetal circulation syndrome", "Persistent Fetal Circulation Syndrome", "persistent pulmonary hypertension of the newborn", "Persistent Pulmonary Hypertension of the Newborn"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "persistent fetal circulation syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0002993", "names": ["somatostatinoma", "Pancreatic Somatostatinoma", "pancreatic somatostatinoma", "islet cell somatostatinoma", "pancreatic Somatostatin cell tumor", "pancreatic somatostatin cell tumor", "pancreatic delta cell somatostatin producing neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic somatostatinoma", "shortest_name_length": 15}
{"curie": "MONDO:0002128", "names": ["Mononeuritis Multiplex", "Mononeuritis multiplex", "mononeuritis multiplex", "MONONEURITIS MULTIPLEX", "Multiple mononeuropathy", "multiplex; mononeuritis", "mononeuritis; multiplex", "Mononeuritis multiplex (disorder)", "mononeuritis multiplex (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mononeuritis multiplex", "shortest_name_length": 22}
{"curie": "UMLS:C1112257", "names": ["Oral pustule"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral pustule", "shortest_name_length": 12}
{"curie": "UMLS:C4329692", "names": ["Craniotubular Hyperostosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Craniotubular Hyperostosis", "shortest_name_length": 26}
{"curie": "UMLS:C1332281", "names": ["Grade 3 Diencephalic Astrocytoma", "Grade III Diencephalic Astrocytoma", "Diencephalic Anaplastic Astrocytoma", "Anaplastic Diencephalic Astrocytoma", "Grade 3 Astrocytoma of Diencephalon", "Grade 3 Diencephalic Astrocytic Tumor", "Grade III Astrocytoma of Diencephalon", "Anaplastic Astrocytoma of Diencephalon", "Grade III Diencephalic Astrocytic Tumor", "Grade 3 Astrocytoma of the Diencephalon", "Grade 3 Diencephalic Astrocytic Neoplasm", "Grade 3 Astrocytic Tumor of Diencephalon", "Undifferentiated Diencephalic Astrocytoma", "Grade III Astrocytoma of the Diencephalon", "Grade III Astrocytic Tumor of Diencephalon", "Grade III Diencephalic Astrocytic Neoplasm", "Anaplastic Astrocytoma of the Diencephalon", "Grade 3 Astrocytic Neoplasm of Diencephalon", "Undifferentiated Astrocytoma of Diencephalon", "Grade 3 Astrocytic Tumor of the Diencephalon", "Grade III Astrocytic Neoplasm of Diencephalon", "Grade III Astrocytic Tumor of the Diencephalon", "Grade 3 Astrocytic Neoplasm of the Diencephalon", "Undifferentiated Astrocytoma of the Diencephalon", "Grade III Astrocytic Neoplasm of the Diencephalon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anaplastic Diencephalic Astrocytoma", "shortest_name_length": 32}
{"curie": "MONDO:0016506", "names": ["ectopic aldosterone-producing tumor", "Extra-adrenal aldosterone-producing tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectopic aldosterone-producing tumor", "shortest_name_length": 35}
{"curie": "MONDO:0025487", "names": ["MAIDS", "murine AIDS", "AIDS, murine", "murine AIDSs", "murine acquired immunodeficiency syndrome", "Murine Acquired Immunodeficiency Syndrome", "murine acquired immuno-deficiency syndrome", "murine acquired immune deficiency syndrome", "murine acquired immuno deficiency syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "murine acquired immunodeficiency syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C5418577", "names": ["Skin Spindle Cell Lipoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin Spindle Cell Lipoma", "shortest_name_length": 24}
{"curie": "UMLS:C2919886", "names": ["Struvite urolithiasis", "Struvite Urolithiasis", "Magnesium ammonium phosphate urolithiasis", "Ammonium magnesium phosphate urolithiasis", "Magnesium Ammonium Phosphate Urolithiasis", "Magnesium ammonium phosphate urolithiasis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Magnesium ammonium phosphate urolithiasis", "shortest_name_length": 21}
{"curie": "MONDO:0006363", "names": ["BMPM", "Multicystic mesothelioma", "multicystic mesothelioma", "multilocular peritoneal cysts", "Peritoneal cystic mesothelioma", "peritoneal cystic mesothelioma", "Cystic mesothelioma of peritoneum", "peritoneal multicystic mesothelioma", "Peritoneal Multicystic Mesothelioma", "benign cystic peritoneal mesothelioma", "Multilocular Peritoneal Inclusion Cyst", "multicystic mesothelioma of peritoneum", "multilocular peritoneal inclusion cyst", "Multicystic Mesothelioma of Peritoneum", "Multilocular peritoneal inclusion cyst", "multilocular peritoneal inclusion cysts", "benign multicystic peritoneal mesothelioma", "Multicystic Mesothelioma of the Peritoneum", "multicystic mesothelioma of the peritoneum", "Benign multicystic peritoneal mesothelioma", "Cystic mesothelioma of peritoneum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peritoneal multicystic mesothelioma", "shortest_name_length": 4}
{"curie": "MONDO:0008020", "names": ["spasticity multiple exostoses", "Hamann Zanki schimrigk syndrome", "multiple exostoses with spastic tetraparesis", "Multiple Exostoses with Spastic Tetraparesis", "MULTIPLE EXOSTOSES WITH SPASTIC TETRAPARESIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple exostoses with spastic tetraparesis", "shortest_name_length": 29}
{"curie": "MONDO:0021680", "names": ["Strep", "STREP INFECTION", "strep infection", "Streptococcosis", "Streptococcal Infection", "STREPTOCOCCAL INFECTION", "streptococcal infection", "streptococcus infection", "Infection;streptococcal", "Streptococcus infection", "Streptococcal infection", "Infection, Streptococcal", "STREPTOCOCCAL INFECTIONS", "Streptococcal infections", "infection, streptococcal", "streptococcal; infection", "streptococcal infections", "infection; streptococcal", "Streptococcal Infections", "infections, streptococcal", "Infections, Streptococcal", "Streptococcal infection NOS", "Streptococcal infection, NOS", "Streptococcus infectious disease", "streptococcus bacteria infection", "Streptococcal infectious disease", "Streptococcus disease or disorder", "Streptococcal infection (diagnosis)", "Streptococcal infection, unspecified", "Streptococcal infectious disease, NOS", "Streptococcus caused disease or disorder", "Streptococcal infectious disease (disorder)", "Bacterial infection due to unspecified streptococcus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "streptococcal infection", "shortest_name_length": 5}
{"curie": "MONDO:0024564", "names": ["Crmcc", "CRMCC1", "Coats plus syndrome", "CTC1 Coats plus syndrome", "Coats plus syndrome caused by mutation in CTC1", "cerebroretinal microangiopathy with calcifications and cysts", "cerebroretinal microangiopathy with calcifications and cysts 1", "CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebroretinal microangiopathy with calcifications and cysts 1", "shortest_name_length": 5}
{"curie": "UMLS:C0027626", "names": ["Neoplasm Invasion", "Invasion, Neoplasm", "neoplasm invasiveness", "Neoplasm Invasiveness", "Invasiveness, Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplasm Invasiveness", "shortest_name_length": 17}
{"curie": "MONDO:0008301", "names": ["Guttmacher syndrome", "GUTTMACHER SYNDROME", "Preaxial deficiency, postaxial polydactyly and hypospadias", "preaxial deficiency, postaxial polydactyly and hypospadias", "preaxial deficiency, postaxial polydactyly, and hypospadias", "Preaxial Deficiency, Postaxial Polydactyly, And Hypospadias", "PREAXIAL DEFICIENCY, POSTAXIAL POLYDACTYLY, AND HYPOSPADIAS", "preaxial deficiency-postaxial polydactyly-hypospadias syndrome", "Preaxial deficiency-postaxial polydactyly-hypospadias syndrome", "Preaxial deficiency, postaxial polydactyly, hypospadias syndrome", "Preaxial deficiency, postaxial polydactyly, hypospadias syndrome (disorder)", "autosomal dominant preaxial deficiency, postaxial polydactyly, and hypospadias", "Autosomal dominant preaxial deficiency, postaxial polydactyly, and hypospadias"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Guttmacher syndrome", "shortest_name_length": 19}
{"curie": "UMLS:C2938915", "names": ["Gliomatosis Peritonei", "Peritoneal gliomatosis", "Peritoneal Gliomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peritoneal gliomatosis", "shortest_name_length": 21}
{"curie": "MONDO:0012727", "names": ["Kd", "KD", "MLNS", "MCLS", "Kawasaki", "Kawasaki disease", "kawasaki disease", "Disease;Kawasaki", "Kawasaki Disease", "KAWASAKI DISEASE", "Kawasaki Syndrome", "kawasaki syndrome", "Kawasaki syndrome", "acute febrile MCLS", "kawasakis syndrome", "Acute febrile MCLS", "Kawasaki's disease", "kawasaki's disease", "kawasaki's syndrome", "Kawasaki's syndrome", "infantile polyarteritis", "INFANTILE POLYARTERITIS", "Infantile polyarteritis", "Kawasaki disease (diagnosis)", "Infantile Polyarteritis Nodosa", "infantile polyarteritis nodosa", "INFANTILE POLYARTERITIS NODOSA", "mucocutaneous lymph node syndrome", "Mucocutaneous Lymph Node Syndrome", "Mucocutaneous lymph node syndrome", "MUCOCUTANEOUS LYMPH NODE SYNDROME", "mucocutaneous lymph node; syndrome", "syndrome; mucocutaneous lymph node", "Lymph Node Syndrome, Mucocutaneous", "Kawasakis mucocutaneous lymph node syndrome", "Mucocutaneous lymph node syndrome [Kawasaki]", "Acute febrile mucocutaneous lymph node syndrome", "acute febrile mucocutaneous lymph node syndrome", "Acute febrile mucocutaneous lymph node syndrome [MCLS]", "acute febrile mucocutaneous lymph node syndrome [MCLS]", "Acute febrile mucocutaneous lymph node syndrome (MCLS)", "Acute febrile mucocutaneous lymph node syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucocutaneous lymph node syndrome", "shortest_name_length": 2}
{"curie": "MONDO:0021513", "names": ["benign tonsil tumor", "Benign Tonsil Tumor", "Benign Tonsil Neoplasm", "tonsil benign neoplasm", "Benign Tumor of Tonsil", "benign tonsillar tumor", "benign tonsil neoplasm", "benign tumor of tonsil", "Benign tumor of tonsil", "Benign Tonsillar Tumor", "Benign tumour of tonsil", "Benign Tonsillar Neoplasm", "Tonsillar neoplasm benign", "Benign neoplasm of tonsil", "benign tonsillar neoplasm", "benign neoplasm of tonsil", "Benign tonsillar neoplasm", "Benign Neoplasm of Tonsil", "tonsillar neoplasm, benign", "benign tumor of the tonsil", "Benign Tumor of the Tonsil", "Tonsillar Neoplasm, Benign", "Benign neoplasm of the tonsil", "benign neoplasm of the tonsil", "Benign Neoplasm of the Tonsil", "Benign tumor of faucial tonsil", "Benign tumor of palatine tonsil", "Benign tumour of faucial tonsil", "Benign tumour of palatine tonsil", "Benign neoplasm of palatine tonsil", "Benign neoplasm of tonsil (disorder)", "benign neoplasm of tonsil (diagnosis)", "Benign neoplasm of the faucial tonsil", "Benign neoplasm of the palatine tonsil"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of tonsil", "shortest_name_length": 19}
{"curie": "UMLS:C2347912", "names": ["Recurrent Spinal Cord Neoplasm", "Recurrent Adult Spinal Cord Tumor", "recurrent adult spinal cord tumor", "recurrent adult spinal cord neoplasm", "Recurrent Adult Spinal Cord Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Adult Spinal Cord Neoplasm", "shortest_name_length": 30}
{"curie": "UMLS:C0346056", "names": ["NMC", "Triton tumor", "Triton tumour", "Nerve Rhabdomyoma", "Benign Triton tumor", "Benign Triton Tumor", "Benign Triton tumour", "Rhabdomyoma/Choristoma", "Neuromuscular Hamartoma", "Neuromuscular hamartoma", "Neuromuscular Choristoma", "Ectomesenchymal Hamartoma", "Neuromuscular hamartoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neuromuscular hamartoma", "shortest_name_length": 3}
{"curie": "MONDO:0004060", "names": ["Classic Epithelioid Sarcoma", "Peripheral Epithelioid Sarcoma", "peripheral epithelioid sarcoma", "Distal-Type Epithelioid Sarcoma", "distal-type epithelioid sarcoma", "conventional epithelioid sarcoma", "Conventional Epithelioid Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peripheral epithelioid sarcoma", "shortest_name_length": 27}
{"curie": "MONDO:0006979", "names": ["Steatitis", "steatitis", "Steatitides", "Pansteatitis", "Yellow fat disease", "Inflammation of fat", "Nutritional Steatitis", "Nutritional steatitis", "Nutritional Panniculitis", "Nutritional panniculitis", "Inflammation of adipose tissue", "Nutritional steatitis (disorder)", "Inflammation of adipose tissue (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "steatitis", "shortest_name_length": 9}
{"curie": "UMLS:C5418909", "names": ["Locally Advanced Thyroid Gland Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Thyroid Gland Carcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0011737", "names": ["AAOPD", "PARK10", "parkinson disease 10", "Parkinson Disease 10", "Parkinson disease 10", "PARKINSON DISEASE 10", "Parkinson disease, Age at onset of", "PARKINSON DISEASE, AGE AT ONSET OF", "Parkinson Disease, Age At Onset Of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parkinson disease 10", "shortest_name_length": 5}
{"curie": "MONDO:0043199", "names": ["Colavita Kozlowski syndrome", "Short limb dwarf lethal Colavita Kozlowski type", "short limb dwarf lethal colavita kozlowski type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short limb dwarf lethal colavita kozlowski type", "shortest_name_length": 27}
{"curie": "MONDO:0001226", "names": ["blight", "Blight", "blights", "pinkeye", "PINKEYE", "Pinkeye", "Pink eye", "blighted", "PINK EYE", "Bovine pinkeye", "New Forest disease", "Contagious opthalmia", "conjunctivitis infective", "Conjunctivitis infective", "Bovine infectious ophthalmia", "CONJUNCTIVITIS, SIMPLE, ACUTE", "Acute contagious conjunctivitis", "Acute Contagious Conjunctivitis", "acute contagious conjunctivitis", "Infection due to Moraxella bovis", "CONJUNCTIVITIS, CATARRHAL, ACUTE", "Bovine infectious keratoconjunctivitis", "Infectious bovine keratoconjunctivitis", "Keratoconjunctivitis due to Moraxella bovis", "keratoconjunctivitis caused by Moraxella bovis", "Keratoconjunctivitis caused by Moraxella bovis", "Keratoconjunctivitis caused by Moraxella bovis (disorder)", "keratoconjunctivitis caused by Moraxella bovis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute contagious conjunctivitis", "shortest_name_length": 6}
{"curie": "UMLS:C0278570", "names": ["Skin T-Cell Lymphoma Stage III", "T-Cell Lymphoma of Skin Stage III", "stage III cutaneous T-cell lymphoma", "Cutaneous T-Cell Lymphoma Stage III", "Cutaneous T-cell lymphoma stage III", "cutaneous T-cell lymphoma, stage III", "T-Cell Lymphoma of the Skin Stage III", "Stage III Cutaneous T-Cell Non-Hodgkin Lymphoma", "Stage III Cutaneous T-Cell Non-Hodgkin's Lymphoma", "Stage III Cutaneous (Skin) T-Cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Cutaneous T-Cell Non-Hodgkin Lymphoma", "shortest_name_length": 30}
{"curie": "MONDO:0005351", "names": ["Anorexia Nervosa", "ANOREXIA NERVOSA", "Anorexia nervosa", "anorexia nervosa", "anorexia; nervosa", "anorexia mentalis", "Anorexia Nervosas", "nervosa; anorexia", "Nervosa, Anorexia", "ANOREXIA, NERVOSA", "Anorexia mentalis", "Nervosas, Anorexia", "AN - Anorexia nervosa", "Anorexia nervosa (disorder)", "anorexia nervosa (diagnosis)", "Anorexia nervosa, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anorexia nervosa", "shortest_name_length": 16}
{"curie": "UMLS:C0855146", "names": ["B-Lymphoblastic Lymphoma", "B Lymphoblastic Lymphoma", "Precur. B-lymphoblastic lymphoma", "Precursor B-lymphoblastic lymphoma", "Precursor B-Lymphoblastic Lymphoma", "Precursor B-lymphoblastic lymphomas", "Precursor B-lymphoblastic lymphoma NOS", "precursor B-cell lymphoblastic lymphoma", "Precursor B-cell lymphoblastic lymphoma", "precursor B-cell lymphoblastic lymphoma (diagnosis)", "malignant neoplasm lymphoma B-cell precursor lymphoblastic", "Precursor B-cell lymphoblastic lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B Lymphoblastic Lymphoma", "shortest_name_length": 24}
{"curie": "UMLS:C4744440", "names": ["Unresectable Digestive System Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Digestive System Carcinoma", "shortest_name_length": 39}
{"curie": "UMLS:C1262162", "names": ["Oral administration complication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral administration complication", "shortest_name_length": 32}
{"curie": "MONDO:0005549", "names": ["RCC", "renal cell cancer", "Renal Cell Cancer", "Renal Cell Carcinoma", "renal cell carcinoma", "kidney adenocarcinoma", "Kidney Adenocarcinoma", "adenocarcinoma of kidney", "Adenocarcinoma of Kidney", "renal cell adenocarcinoma", "Renal cell adenocarcinoma", "Renal Cell Adenocarcinoma", "Renal cell carcinoma, NOS", "Adenocarcinoma of the Kidney", "adenocarcinoma of the kidney", "carcinoma, renal cell, malignant", "CARCINOMA, RENAL CELL, MALIGNANT", "Renal cell carcinoma, unclassified", "renal cell carcinoma, stage unspecified", "Renal Cell Carcinoma, Stage Unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal cell adenocarcinoma", "shortest_name_length": 3}
{"curie": "UMLS:C4744567", "names": ["Metastatic Thyroid Gland Follicular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Thyroid Gland Follicular Carcinoma", "shortest_name_length": 45}
{"curie": "UMLS:C0598784", "names": ["dyslipoproteinemia", "Dyslipoproteinemia", "Dyslipoproteinaemia", "Dyslipoproteinemias"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dyslipoproteinemias", "shortest_name_length": 18}
{"curie": "MONDO:0015231", "names": ["Bartter", "bartter disease", "barters disease", "Bartter Disease", "Bartter disease", "Bartters Disease", "Bartter Syndrome", "BARTTER SYNDROME", "bartter syndrome", "Bartter syndrome", "barter's disease", "bartter's disease", "disease bartter's", "Syndrome, Bartter", "Bartters Syndrome", "bartters syndrome", "BARTTERS SYNDROME", "Bartter's Disease", "Potassium wasting", "bartter's syndrome", "Bartter's syndrome", "Bartter's Syndrome", "Syndrome, Bartter's", "bartters's syndrome", "HYPOKALEMIC ALKALOSIS", "Bartter syndrome (BS)", "Hypokalemic alkalosis", "Hypokalemic Alkalosis", "ALKALOSIS HYPOKALEMIC", "Alkalosis hypokalemic", "hypokalemic alkalosis", "Alkalosis, hypokalemic", "Hypokalaemic alkalosis", "Alkalosis hypokalaemic", "Bartter syndrome (disorder)", "Bartter syndrome (diagnosis)", "Hypokalemic alkalosis (disorder)", "juxtaglomerular hyperplasia syndrome", "hypokalemic alkalosis with hypercalciuria", "Salt-wasting tubulopathy, Henle's loop type", "salt-wasting tubulopathy, Henle's loop type", "aldosteronism-normal blood pressure syndrome", "salt-losing tubular disorder, Henle's loop type", "Salt-losing tubular disorder, Henle's loop type", "aldosteronism with hyperplasia of the adrenal cortex", "Aldosteronism with hyperplasia of the adrenal cortex", "Aldosteronism with Hyperplasia of the Adrenal Cortex", "Juxtaglomerular hyperplasia with secondary aldosteronism", "JUXTAGLOMERULAR HYPERPLASIA WITH SECONDARY ALDOSTERONISM", "Juxtaglomerular Hyperplasia with Secondary Aldosteronism", "Bartter syndrome with hypercalciuria and nephrocalcinosis", "Bartter's syndrome with hypercalciuria and nephrocalcinosis", "renal tubular normotensive hypokalemic alkalosis with hypercalciuria", "Renal tubular normotensive hypokalemic alkalosis with hypercalciuria", "Syndrome of juxtaglomerular hyperplasia with secondary aldosteronism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bartter syndrome", "shortest_name_length": 7}
{"curie": "MONDO:0014923", "names": ["PSS5", "PEELING SKIN SYNDROME 5", "peeling skin syndrome 5", "peeling skin syndrome type 5", "peeling skin syndrome 5; PSS5", "SERPINB8 peeling skin syndrome", "peeling skin syndrome caused by mutation in SERPINB8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peeling skin syndrome 5", "shortest_name_length": 4}
{"curie": "MONDO:0009035", "names": ["CMDR", "Autosomal Recessive Craniometaphyseal Dysplasia", "autosomal recessive craniometaphyseal dysplasia", "CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE", "craniometaphyseal dysplasia, autosomal recessive", "Craniometaphyseal Dysplasia, Autosomal Recessive", "Craniometaphyseal dysplasia, autosomal recessive type", "craniometaphyseal dysplasia, autosomal recessive type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniometaphyseal dysplasia, autosomal recessive", "shortest_name_length": 4}
{"curie": "MONDO:0010152", "names": ["OMCS", "Congenital trichomegaly", "OLIVER-MCFARLANE SYNDROME", "Oliver McFarlane syndrome", "Oliver-McFarlane syndrome", "Eyelashes long mental retardation", "eyelashes long mental retardation", "EYELASHES, LONG, WITH MENTAL RETARDATION", "eyelashes, long, with mental retardation", "eyelashes, long with intellectual disability", "eyelashes, long, with intellectual disability", "Long eyelashes-intellectual disability syndrome", "long eyelashes-intellectual disability syndrome", "Trichomegaly retina pigmentary degeneration dwarfism", "Trichomegaly-retina pigmentary degeneration-dwarfism syndrome", "trichomegaly-retina pigmentary degeneration-dwarfism syndrome", "Trichomegaly with retina pigmentary degeneration and dwarfism syndrome", "Congenital trichomegaly, pigmentary retinal degeneration, and short stature", "Trichomegaly with retina pigmentary degeneration and dwarfism syndrome (disorder)", "trichomegaly with mental retardation, dwarfism, and pigmentary Degeneration of retina", "TRICHOMEGALY WITH MENTAL RETARDATION, DWARFISM, AND PIGMENTARY DEGENERATION OF RETINA", "trichomegaly with intellectual disability, dwarfism and pigmentary degeneration of retina", "trichomegaly with intellectual disability, dwarfism, and pigmentary Degeneration of retina"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichomegaly-retina pigmentary degeneration-dwarfism syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0015180", "names": ["intestinal disease due to fat malabsorption"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intestinal disease due to fat malabsorption", "shortest_name_length": 43}
{"curie": "MONDO:0018826", "names": ["MADSAM", "Lewis-Sumner syndrome", "Multifocal acquired demyelinating sensory and motor neuropathy", "multifocal acquired demyelinating sensory and motor neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lewis-Sumner syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C1334963", "names": ["Nevoid Basal Cell Carcinoma Syndrome Associated Medulloblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nevoid Basal Cell Carcinoma Syndrome Associated Medulloblastoma", "shortest_name_length": 63}
{"curie": "MONDO:0009188", "names": ["epilepsy telangiectasia", "Epilepsy telangiectasia", "Epilepsy-Telangiectasia", "EPILEPSY-TELANGIECTASIA", "epilepsy-telangiectasia", "epilepsy-telangiectasia syndrome", "mental retardation, epilepsy, palpebral conjunctival telangiectasias and IgA deficiency", "intellectual disability, epilepsy, palpebral conjunctival telangiectasias and IgA deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy-telangiectasia syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0015829", "names": ["isolated uterovaginal malformation", "nonsyndromic uterovaginal malformation", "non-syndromic uterovaginal malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-syndromic uterovaginal malformation", "shortest_name_length": 34}
{"curie": "MONDO:0002017", "names": ["OPCA", "syndrome thomas", "Presenile Ataxia", "Thomas' syndrome", "Ataxia, Presenile", "Presenile Ataxias", "Ataxias, Presenile", "WADIA-swami syndrome", "WADIA-SWAMI SYNDROME", "Olivocerebellar atrophy", "olivocerebellar atrophy", "Déjerine-Thomas atrophy", "DEJERINE-THOMAS ATROPHY", "Dejerine-Thomas syndrome", "Dejerine-Thomas Syndrome", "Dejerine Thomas Syndrome", "Déjérine-Thomas syndrome", "atrophy; Déjerine-Thomas", "Déjerine-Thomas; atrophy", "PRESENILE ATAXIA SYNDROME", "Syndrome, Dejerine-Thomas", "Olivopontocerebellar atrophy", "Pontoolivocerebellar Atrophy", "Olivopontocerebellar Atrophy", "OLIVOPONTOCEREBELLAR ATROPHY", "olivopontocerebellar atrophy", "Atrophy, Pontoolivocerebellar", "atrophy; olivopontocerebellar", "Atrophy, Olivopontocerebellar", "olivopontocerebellar; atrophy", "Pontoolivocerebellar Atrophies", "Olivo Ponto Cerebellar Atrophy", "olivopontocerebellar atrophies", "olivo ponto cerebellar atrophy", "atrophy cerebellar olivo ponto", "Olivopontocerebellar Atrophies", "Olivo-Ponto-Cerebellar Atrophy", "Olivopontocerebellar atrophies", "Atrophy, Olivo-Ponto-Cerebellar", "OLIVOPONTOCEREBELLAR DEGENERATION", "Olivopontocerebellar degeneration", "Olivopontocerebellar Degeneration", "Degeneration, Olivopontocerebellar", "Olivopontocerebellar Degenerations", "olivopontocerebellar; degeneration", "degeneration; olivopontocerebellar", "Degenerations, Olivopontocerebellar", "Olivo-Ponto-Cerebellar Degeneration", "Olivo Ponto Cerebellar Degeneration", "olivocerebellar atrophy (diagnosis)", "OPCA - Olivopontocerebellar atrophy", "Degeneration, Olivo-Ponto-Cerebellar", "Olivo-Ponto-Cerebellar Degenerations", "Degenerations, Olivo-Ponto-Cerebellar", "olivopontocerebellar atrophy (diagnosis)", "Olivopontocerebellar degeneration (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "olivopontocerebellar atrophy", "shortest_name_length": 4}
{"curie": "UMLS:C0677712", "names": ["Stage III Indolent Non-Hodgkin Lymphoma", "Stage III Indolent Adult Non-Hodgkin Lymphoma", "stage III indolent adult non-Hodgkin lymphoma", "indolent, stage III adult non-Hodgkin lymphoma", "stage III indolent adult non-Hodgkin's lymphoma", "Indolent Stage III Adult Non-Hodgkin's Lymphoma", "Indolent Adult Non-Hodgkin's Lymphoma Stage III", "Stage III Indolent Adult Non-Hodgkin's Lymphoma", "indolent adult non-Hodgkin's lymphoma stage III", "indolent stage III adult non-Hodgkin's lymphoma", "Ann Arbor Stage III Indolent Adult Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Indolent Adult Non-Hodgkin Lymphoma", "shortest_name_length": 39}
{"curie": "UMLS:C4085634", "names": ["Aorticopulmonary Septal Defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aorticopulmonary Septal Defect", "shortest_name_length": 30}
{"curie": "MONDO:0014086", "names": ["OI15", "OI, TYPE XV", "OI, type 15", "WNT1 osteogenesis imperfecta", "osteogenesis imperfecta type 15", "osteogenesis imperfecta type XV", "OSTEOGENESIS IMPERFECTA, TYPE XV", "osteogenesis imperfecta, type 15", "osteogenesis imperfecta, type XV", "osteogenesis imperfecta caused by mutation in WNT1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteogenesis imperfecta type 15", "shortest_name_length": 4}
{"curie": "MONDO:0032813", "names": ["DEE79", "EIEE79", "early infantile epileptic encephalopathy 79", "epileptic encephalopathy, early infantile, 79", "developmental and epileptic encephalopathy 79", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 79", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 79", "developmental and epileptic encephalopathy, 79"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 79", "shortest_name_length": 5}
{"curie": "MONDO:0020707", "names": ["Central deafness", "Deafness, central", "central hearing loss", "Central Hearing Loss", "Central hearing loss", "Hearing Loss, Central", "Central hearing loss NOS", "Central Auditory Disease", "Central Auditory Diseases", "Auditory Disease, Central", "Auditory Diseases, Central", "Central auditory dysfunction", "Central Auditory Dysfunction", "Auditory Dysfunction, Central", "Dysfunction, Central Auditory", "Dysfunctions, Central Auditory", "Central hearing loss (disorder)", "central hearing loss (diagnosis)", "Central Auditory Pathway Disorders", "Auditory Pathway Disorders, Central"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central hearing loss", "shortest_name_length": 16}
{"curie": "MONDO:0007989", "names": ["MCOR", "Mcor", "Pinhole pupils", "pinhole pupils", "Congenital miosis", "congenital miosis", "MIOSIS, CONGENITAL", "miosis, congenital", "Miosis, congenital", "Congenital microcoria", "congenital microcoria", "Microcoria, congenital", "microcoria, congenital", "MICROCORIA, CONGENITAL", "Congenital miosis (disorder)", "chromosome 13Q32 deletion syndrome", "CHROMOSOME 13q32 DELETION SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital microcoria", "shortest_name_length": 4}
{"curie": "UMLS:C1334002", "names": ["DIN 3", "DCIS Grade 3", "Breast Comedocarcinoma", "Comedocarcinoma of breast", "comedocarcinoma of breast", "High-Grade DCIS of Breast", "High-Grade DCIS of the Breast", "comedo ductal breast carcinoma", "ductal comedo breast carcinoma", "grade III ductal carcinoma in situ", "comedocarcinoma of breast (diagnosis)", "Ductal Intraepithelial Neoplasia, Grade 3", "High Grade Ductal Breast Carcinoma In Situ", "Breast Ductal Carcinoma In Situ, High Grade", "High-Grade Ductal Carcinoma In Situ of Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Ductal Breast Carcinoma In Situ", "shortest_name_length": 5}
{"curie": "UMLS:C2349019", "names": ["Unfavorable Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unfavorable Hodgkin Lymphoma", "shortest_name_length": 28}
{"curie": "UMLS:C3272485", "names": ["Ampulla of Vater Gangliocytic Paraganglioma", "Gangliocytic Paraganglioma of the Ampullary Region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ampulla of Vater Gangliocytic Paraganglioma", "shortest_name_length": 43}
{"curie": "MONDO:0017549", "names": ["humero-radio-ulnar fusion, bilateral", "humero-radio-ulnar synostosis, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "humero-radio-ulnar synostosis, bilateral", "shortest_name_length": 36}
{"curie": "UMLS:C0269661", "names": ["EMESIS PREGNANCY", "emesis pregnancy", "pregnancy vomits", "pregnancy emesis", "Vomiting;pregnancy", "vomiting pregnancy", "pregnancy vomiting", "pregnancy; vomiting", "vomiting of pregnancy", "vomiting in pregnancy", "Vomiting in pregnancy", "Vomiting of pregnancy", "vomiting during pregnancy", "Vomiting of pregnancy, NOS", "Vomiting of pregnancy (disorder)", "vomiting of pregnancy (diagnosis)", "Unspecified vomiting of pregnancy", "vomiting associated with pregnancy", "Vomiting of pregnancy, unspecified", "vomiting during pregnancy (symptom)", "Vomiting as reason for care in pregnancy", "Vomiting as reason for care in pregnancy, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vomiting of pregnancy", "shortest_name_length": 16}
{"curie": "UMLS:C1335720", "names": ["Recurrent Primitive Neuroectodermal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Primitive Neuroectodermal Tumor", "shortest_name_length": 41}
{"curie": "MONDO:0700166", "names": ["CTVT", "Canine Transmissible Venereal Tumor", "canine transmissible venereal tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canine transmissible venereal tumor", "shortest_name_length": 4}
{"curie": "MONDO:0017329", "names": ["Familial VUR", "familial VUR", "Familial vesicoureteral reflux", "familial vesicoureteral reflux", "Familial vesicoureteral reflux (disorder)", "hereditary vesicoureteral reflux (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial vesicoureteral reflux", "shortest_name_length": 12}
{"curie": "UMLS:C4727103", "names": ["Metastatic Colorectal Cancer in the Lung", "Colorectal Carcinoma Metastatic in the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Carcinoma Metastatic in the Lung", "shortest_name_length": 40}
{"curie": "MONDO:0100013", "names": ["paratenonitis with tendinosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paratenonitis with tendinosis", "shortest_name_length": 29}
{"curie": "MONDO:0006936", "names": ["pulmonic stenosis", "PULMONIC STENOSIS", "Pulmonic stenosis", "Pulmonic Stenoses", "Pulmonic Stenosis", "Pulmonary Stenose", "Pulmonic stenosis.", "Pulmonary Stenoses", "Stenoses, Pulmonic", "Pulmonary Stenosis", "pulmonary stenosis", "Stenose, Pulmonary", "Stenosis, Pulmonic", "Pulmonary stenosis", "stenosis pulmonary", "pulmonary; stenosis", "Stenosis, Pulmonary", "Stenoses, Pulmonary", "Pulmonic stenosis NOS", "STENOSIS PULMONIC VALVE", "PULMONIC VALVE STENOSIS", "Stenosis pulmonic valve", "stenosis pulmonic valve", "Pulmonic Valve Stenosis", "Pulmonic valve stenosis", "pulmonic valve stenosis", "PULMONARY VALVE STENOSIS", "Pulmonary Valve Stenoses", "Pulmonary valve stenosis", "pulmonary valve stenosis", "Pulmonary Valve Stenosis", "pulmonary stenosis valve", "Stenosis, Pulmonary Valve", "Pulmonary valve--Stenosis", "pulmonary valve; stenosis", "PULMONARY VALVE, STENOSIS", "Stenoses, Pulmonary Valve", "stenosis; pulmonary valve", "valvular pulmonic stenosis", "Valvular pulmonic stenosis", "pulmonary valve; stricture", "PULMONIC VALVULAR STENOSIS", "pulmonic valvular stenosis", "pulmonary; stenosis, valve", "Valvular Pulmonic Stenosis", "Valvular Pulmonic Stenoses", "stricture; pulmonary valve", "Pulmonic Stenosis, Valvular", "Narrowing of pulmonic valve", "Pulmonic Stenoses, Valvular", "Pulmonic valve stenosis, NOS", "PS - Pulmonary valve stenosis", "PVS - Pulmonary valve stenosis", "PULMONARY VALVE, STENOSIS, PURE", "Pulmonic valve stenosis (disorder)", "pulmonary; stricture pulmonary valve", "pulmonary valve stenosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary valve stenosis", "shortest_name_length": 17}
{"curie": "UMLS:C5206129", "names": ["Metastatic BRCA-Mutated Breast Carcinoma", "BRCA-Mutated Metastatic Breast Carcinoma", "Metastatic BRCA-Associated Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic BRCA-Associated Breast Carcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0003129", "names": ["Epithelial Predominant Pulmonary Blastoma", "epithelial predominant pulmonary blastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epithelial predominant pulmonary blastoma", "shortest_name_length": 41}
{"curie": "UMLS:C5667322", "names": ["Metastatic Conjunctival Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Conjunctival Melanoma", "shortest_name_length": 32}
{"curie": "MONDO:0011058", "names": ["DFNA9", "autosomal dominant deafness 9", "deafness, autosomal dominant 9", "DEAFNESS, AUTOSOMAL DOMINANT 9", "Deafness, Autosomal Dominant 9", "deafness, autosomal dominant type 9", "autosomal dominant nonsyndromic deafness 9", "COCH autosomal dominant nonsyndromic deafness", "autosomal dominant nonsyndromic hearing loss 9", "autosomal dominant nonsyndromic deafness type 9", "autosomal dominant nonsyndromic deafness caused by mutation in COCH"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 9", "shortest_name_length": 5}
{"curie": "MONDO:0008937", "names": ["CEREBELLAR ATAXIA, BENIGN, WITH THERMOANALGESIA", "cerebellar ataxia, benign, with thermoanalgesia", "Cerebellar Ataxia, Benign, with Thermoanalgesia", "Cerebellar Ataxia with Loss of Pain and Temperature Sensation", "CEREBELLAR ATAXIA WITH LOSS OF PAIN AND TEMPERATURE SENSATION", "cerebellar ataxia with loss of pain and temperature sensation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellar ataxia, benign, with thermoanalgesia", "shortest_name_length": 47}
{"curie": "MONDO:0011346", "names": ["XAN2", "type 2 xanthinuria", "xanthinuria type 2", "xanthinuria type II", "Xanthinuria type II", "xanthinuria, type 2", "type II xanthinuria", "Xanthinuria, Type II", "XANTHINURIA, TYPE II", "xanthinuria, type II", "XDH and AOX dual deficiency", "xanthine dehydrogenase and aldehyde oxidase combined deficiency of", "Xanthine Dehydrogenase and Aldehyde Oxidase, Combined Deficiency of", "xanthine dehydrogenase and aldehyde oxidase, combined deficiency of", "XANTHINE DEHYDROGENASE AND ALDEHYDE OXIDASE, COMBINED DEFICIENCY OF", "Xanthine dehydrogenase and xanthine aldehyde oxidase dual deficiency", "xanthine dehydrogenase and xanthine aldehyde oxidase dual deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "xanthinuria type II", "shortest_name_length": 4}
{"curie": "MONDO:0001575", "names": ["gonococcal salpingitis", "Gonococcal salpingitis", "Chronic gonococcal salpingitis", "Gonococcal salpingitis chronic", "chronic gonococcal salpingitis", "Salpingitis gonococcal chronic", "gonococcal salpingitis, chronic", "Gonococcal salpingitis (chronic)", "Chronic gonococcal salpingitis (disorder)", "chronic gonococcal salpingitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic gonococcal salpingitis", "shortest_name_length": 22}
{"curie": "MONDO:0025494", "names": ["PRRS", "prrs", "blue-ear pig disease", "Mystery Swine Disease", "mystery swine disease", "blue eared pig disease", "Blue Eared Pig Disease", "blue-eared pig disease", "Blue-Eared Pig Disease", "swine disease, mystery", "Swine Disease, Mystery", "Pig Disease, Blue-Eared", "pig disease, blue-eared", "swine infertility and respiratory syndrome", "Swine Infertility and Respiratory Syndrome", "porcine reproductive and respiratory syndrome", "Porcine Reproductive and Respiratory Syndrome", "Porcine reproductive and respiratory syndrome", "reproductive and respiratory syndrome in pigs", "Porcine Epidemic Abortion and Respiratory Syndrome", "porcine epidemic abortion and respiratory syndrome", "porcine reproductive and respiratory syndrome (PRRS)", "Porcine reproductive and respiratory syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "porcine reproductive and respiratory syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0011037", "names": ["CYSRD", "diffuse cystic renal dysplasia", "Renal dysplasia diffuse cystic", "renal dysplasia diffuse cystic", "Diffuse cystic renal dysplasia", "Renal Dysplasia, Diffuse Cystic", "susceptibility to cystic renal dysplasia", "renal dysplasia, cystic, susceptibility to", "RENAL DYSPLASIA, CYSTIC, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal dysplasia, cystic, susceptibility to", "shortest_name_length": 5}
{"curie": "UMLS:C4054390", "names": ["Cytomegalovirus Associated Nephrotic Syndrome", "Nephrotic Syndrome - Cytomegalovirus Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - Cytomegalovirus Associated", "shortest_name_length": 45}
{"curie": "MONDO:0013350", "names": ["MTDPS4B", "Mngie, Polg-related", "MNGIE, POLG-RELATED", "mitochondrial DNA depletion syndrome 4b", "mitochondrial DNA depletion syndrome type 4b", "mitochondrial DNA depletion syndrome 4B (MNGIE type)", "MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE)", "mitochondrial neurogastrointestinal encephalopathy syndrome", "mitochondrial neurogastrointestinal encephalopathy syndrome, Polg-related", "MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOPATHY SYNDROME, POLG-RELATED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial DNA depletion syndrome 4b", "shortest_name_length": 7}
{"curie": "UMLS:C5203935", "names": ["Unresectable Inflammatory Breast Carcinoma", "Unresectable Breast Inflammatory Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Breast Inflammatory Carcinoma", "shortest_name_length": 42}
{"curie": "UMLS:C0347633", "names": ["liver laceration", "Liver laceration", "laceration liver", "Liver Laceration", "lacerations liver", "hepatic laceration", "Hepatic laceration", "laceration of liver", "Laceration of liver", "Liver Laceration(s)", "Hepatic laceration, NOS", "Laceration of liver, NOS", "Laceration of liver (disorder)", "laceration of liver (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laceration of liver", "shortest_name_length": 16}
{"curie": "MONDO:0003660", "names": ["lymphoma", "Lymphoma", "Adult Lymphoma", "adult lymphoma", "lymphoma of adults"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult lymphoma", "shortest_name_length": 8}
{"curie": "MONDO:0008089", "names": ["Familial neutropenia", "leukopenia benign familial", "Familial benign neutropenia", "Benign familial neutropenia", "Neutropenia, severe chronic", "LEUKOPENIA, BENIGN FAMILIAL", "leukopenia, benign familial", "neutropenia chronic familial", "chronic familial neutropenia", "Chronic familial neutropenia", "Benign familial neutropaenia", "Chronic familial neutropaenia", "neutropenia, chronic familial", "Neutropenia, chronic familial", "NEUTROPENIA, CHRONIC FAMILIAL", "Familial benign chronic neutropenia", "Chronic familial neutropenia (disorder)", "Chronic familial neutropenia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neutropenia, chronic familial", "shortest_name_length": 20}
{"curie": "UMLS:C4302455", "names": ["Obstructive pancreatitis", "Pancreatitis due to pancreatic duct obstruction", "Pancreatitis due to pancreatic duct obstruction (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatitis due to pancreatic duct obstruction", "shortest_name_length": 24}
{"curie": "UMLS:C0086468", "names": ["Prenatal Injury", "Injury, Prenatal", "Prenatal Injuries", "Injuries, Prenatal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prenatal Injuries", "shortest_name_length": 15}
{"curie": "UMLS:C3661933", "names": ["Dyslipidemia due to type 2 diabetes mellitus", "dyslipidemia due to type 2 diabetes mellitus", "Dyslipidemia associated with type II diabetes mellitus", "Dyslipidemia due to type 2 diabetes mellitus (disorder)", "dyslipidemia due to type 2 diabetes mellitus (diagnosis)", "Diabetic dyslipidemia associated with type 2 diabetes mellitus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dyslipidemia due to type 2 diabetes mellitus", "shortest_name_length": 44}
{"curie": "UMLS:C3272821", "names": ["Crohn Disease-Associated Colorectal Adenocarcinoma", "Crohn's Disease-Associated Colorectal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Crohn Disease-Associated Colorectal Adenocarcinoma", "shortest_name_length": 50}
{"curie": "UMLS:C0751533", "names": ["subdural hygroma", "Subdural hygroma", "Subdural Hygroma", "hygroma subdural", "Subdural hydroma", "Hygroma, Subdural", "hygromas subdural", "Subdural hygroma (disorder)", "subdural hygroma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hygroma, Subdural", "shortest_name_length": 16}
{"curie": "MONDO:0025061", "names": ["swine edema disease", "Swine Edema Disease", "Swine Edema Diseases", "swine edema diseases", "edema disease of swine", "Edema Disease of Swine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "edema disease of swine", "shortest_name_length": 19}
{"curie": "MONDO:0006986", "names": ["goiter substernal", "Substernal goitre", "substernal goitre", "substernal goiter", "Substernal Goiter", "Substernal goiter", "Goiter, Substernal", "Substernal Goiters", "GOITER, SUBSTERNAL", "Goiter, substernal", "Retrosternal goiter", "retrosternal goiter", "Retrosternal goitre", "Goiters, Substernal", "goiter retrosternal", "retrosternal goitre", "goiters retrosternal", "Intrathoracic goiter", "GOITER, RETROSTERNAL", "Intrathoracic goitre", "Substernal thyroid goitre", "Substernal thyroid goiter", "retrosternal thyroid goiter", "Retrosternal thyroid goitre", "Retrosternal thyroid goiter", "struma; retrosternal thyroid", "Substernal goiter (disorder)", "retrosternal thyroid; goiter", "substernal goiter (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "substernal goiter", "shortest_name_length": 17}
{"curie": "UMLS:C4684869", "names": ["Refractory Medulloblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Medulloblastoma", "shortest_name_length": 26}
{"curie": "UMLS:C0406519", "names": ["SKIN ULCER INFECTED", "Infected skin ulcer", "Infected ulcer of skin", "skin; infection, ulcer", "infection; skin, ulcer", "cutaneous ulcer with infection", "Infected ulcer of skin (disorder)", "cutaneous ulcer with infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infected ulcer of skin", "shortest_name_length": 19}
{"curie": "MONDO:0024389", "names": ["anaerobic bacterial infection", "Anaerobic bacterial infection", "Anaerobic bacterial infection NOS", "Infection due to anaerobic bacteria", "infection due to anaerobic bacteria", "anaerobic bacteria infectious disease", "Infection caused by anaerobic bacteria", "infection caused by anaerobic bacteria", "infection due to anaerobic bacteria (diagnosis)", "Infection caused by anaerobic bacteria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anaerobic bacteria infectious disease", "shortest_name_length": 29}
{"curie": "MONDO:0020454", "names": ["congenital complete agenesis of pericardium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital complete agenesis of pericardium", "shortest_name_length": 43}
{"curie": "MONDO:0014549", "names": ["LCCS6", "LETHAL CONGENITAL CONTRACTURE SYNDROME 6", "lethal congenital contracture syndrome 6", "lethal congenital contracture syndrome type 6", "ZBTB42 lethal congenital contracture syndrome", "lethal congenital contracture syndrome caused by mutation in ZBTB42"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal congenital contracture syndrome 6", "shortest_name_length": 5}
{"curie": "MONDO:0016015", "names": ["Phenobarbital embryopathy", "phenobarbital embryopathy", "phenobarbital antenatal exposure", "Embryopathy caused by phenobarbital", "Embryopathy caused by phenobarbital (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phenobarbital embryopathy", "shortest_name_length": 25}
{"curie": "MONDO:0016957", "names": ["6q trisomy", "trisomy 6q", "Trisomy 6q", "6q duplication", "Duplication 6q", "partial trisomy 6q", "Chromosome 6, trisomy 6q", "chromosome 6q duplication", "partial trisomy of chromosome 6q", "partial duplication of chromosome 6q", "partial trisomy of the long arm of chromosome 6", "partial duplication of the long arm of chromosome 6", "partial duplication of the long arm of chromosome type 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of the long arm of chromosome 6", "shortest_name_length": 10}
{"curie": "MONDO:0011431", "names": ["OCTD", "MASS syndrome", "MASS SYNDROME", "Mass phenotype", "MASS PHENOTYPE", "MASS phenotype", "overlap connective tissue disease", "Overlap connective tissue disease", "OVERLAP CONNECTIVE TISSUE DISEASE", "Overlapping connective tissue disease", "Mitral valve prolapse, Aortic enlargement, Skin and Skeletal findings"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MASS syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0015708", "names": ["dysplasia immuno osseous", "immuno-osseous dysplasia", "Immuno-osseous dysplasia", "Immuno-osseous dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immuno-osseous dysplasia", "shortest_name_length": 24}
{"curie": "UMLS:C4727421", "names": ["Recurrent Malignant Ovarian Brenner Tumor", "Recurrent Malignant Ovarian Transitional Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Malignant Ovarian Brenner Tumor", "shortest_name_length": 41}
{"curie": "MONDO:0004938", "names": ["Dependence", "dependence", "Dependence on", "dependence on", "substance dependence", "Patient dependence on", "Dependence (qualifier value)", "Patient dependence on (contextual qualifier)", "Patient dependence on (contextual qualifier) (qualifier value)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "substance dependence", "shortest_name_length": 10}
{"curie": "UMLS:C0853968", "names": ["Recurrent Inflammatory Breast Carcinoma", "Recurrent Breast Inflammatory Carcinoma", "Inflammatory carcinoma of breast recurrent", "Recurrent Inflammatory Carcinoma of Breast", "Recurrent Inflammatory Carcinoma of the Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Inflammatory carcinoma of breast recurrent", "shortest_name_length": 39}
{"curie": "UMLS:C5235854", "names": ["Metastatic Renal Pelvis Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Renal Pelvis Carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0009189", "names": ["rMED", "MED4", "EDM4", "epiphyseal dysplasia multiple 4", "multiple epiphyseal dysplasia 4", "Multiple epiphyseal dysplasia 4", "Polyepiphyseal dysplasia type 4", "epiphyseal dysplasia, multiple, 4", "Epiphyseal dysplasia, multiple, 4", "EPIPHYSEAL DYSPLASIA, MULTIPLE, 4", "multiple epiphyseal dysplasia type 4", "Multiple epiphyseal dysplasia type 4", "epiphyseal dysplasia, multiple, type 4", "Multiple epiphyseal dysplasia with clubfoot", "MULTIPLE EPIPHYSEAL DYSPLASIA WITH CLUBFOOT", "multiple epiphyseal dysplasia with clubfoot", "SLC26A2 multiple epiphyseal dysplasia (disease)", "Multiple epiphyseal dysplasia type 4 (disorder)", "Autosomal recessive multiple epiphyseal dysplasia", "autosomal recessive multiple epiphyseal dysplasia", "multiple epiphyseal dysplasia, autosomal recessive", "Multiple epiphyseal dysplasia, autosomal recessive", "MULTIPLE EPIPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE", "multiple epiphyseal dysplasia with bilateral patellae", "multiple epiphyseal dysplasia with Bilayered patellae", "Multiple epiphyseal dysplasia with bilayered patellae", "MULTIPLE EPIPHYSEAL DYSPLASIA WITH BILAYERED PATELLAE", "Multiple epiphyseal dysplasia with double-layered patella", "multiple epiphyseal dysplasia with double-layered patella", "multiple epiphyseal dysplasia (disease) caused by mutation in SLC26A2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple epiphyseal dysplasia type 4", "shortest_name_length": 4}
{"curie": "UMLS:C0266836", "names": ["Colic", "Infant colic", "Infant Colic", "infant colic", "colic infant", "colic infants", "infant; colic", "Colic infantile", "colic infantile", "Infantile Colic", "Infantile colic", "infantile colic", "colics infantile", "Colic, infantile", "Colic, Infantile", "colic; infantile", "Three month colic", "Three-month colic", "Infantile colic - symptom", "Infantile colic (finding)", "infantile colic (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infantile Colic", "shortest_name_length": 5}
{"curie": "UMLS:C5420757", "names": ["Conjunctival Adenosquamous Carcinoma", "Conjunctival Mucoepidermoid Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conjunctival Adenosquamous Carcinoma", "shortest_name_length": 36}
{"curie": "UMLS:C2039417", "names": ["SCH", "Synovial Chondrosarcoma", "synovial chondrosarcoma", "synovial chondrosarcoma of joint", "synovial chondrosarcoma of joint (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "synovial chondrosarcoma of joint", "shortest_name_length": 3}
{"curie": "UMLS:C5447326", "names": ["MSMD", "Mendelian susceptibility to mycobacterial disease", "Mendelian Susceptibility to Mycobacterial Diseases", "Mendelian susceptibility to mycobacterial infection", "MSMD - mendelian susceptibility to mycobacterial disease", "Mendelian susceptibility to mycobacterial disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mendelian susceptibility to mycobacterial disease", "shortest_name_length": 4}
{"curie": "UMLS:C1336365", "names": ["Stage IVB Esophagus Adenocarcinoma", "Stage IVB Esophageal Adenocarcinoma", "Stage IVB Adenocarcinoma of Esophagus", "Stage IVB Adenocarcinoma of the Esophagus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Esophageal Adenocarcinoma", "shortest_name_length": 34}
{"curie": "UMLS:C1336100", "names": ["Stage 0a Renal Pelvis Cancer", "Stage 0a Carcinoma of Renal Pelvis", "Stage 0a Renal Pelvis Cancer AJCC v7", "Stage 0a Carcinoma of the Renal Pelvis", "Stage 0a Renal Pelvis Urothelial Carcinoma", "papillary carcinoma in situ of renal pelvis", "Renal Pelvis Papillary Noninvasive Carcinoma", "Stage 0a Renal Pelvis Urothelial Carcinoma AJCC v7", "papillary carcinoma in situ of renal pelvis (diagnosis)", "renal pelvis carcinoma papillary transitional cell noninvasive", "noninvasive papillary transitional cell carcinoma of renal pelvis", "noninvasive papillary transitional cell carcinoma of renal pelvis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0a Renal Pelvis Cancer AJCC v7", "shortest_name_length": 28}
{"curie": "UMLS:C3146254", "names": ["Stage III Colon Cancer", "Stage III Colon Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Colon Cancer AJCC v7", "shortest_name_length": 22}
{"curie": "UMLS:C0238097", "names": ["cmv encephalitis", "Encephalitis CMV", "Cytomegaloviral encephalitis", "Encephalitis cytomegalovirus", "cytomegalovirus encephalitis", "Cytomegalovirus encephalitis", "ENCEPHALITIS, CYTOMEGALOVIRUS", "Cytomegalovirus encephalitis (disorder)", "cytomegaloviral disease; encephalitis (etiology)", "encephalitis; cytomegaloviral disease (etiology)", "encephalitis; cytomegaloviral disease (manifestation)", "cytomegaloviral disease; encephalitis (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cytomegalovirus encephalitis", "shortest_name_length": 16}
{"curie": "UMLS:C0278681", "names": ["metastatic parathyroid cancer", "Metastatic Parathyroid Cancer", "parathyroid cancer, metastatic", "metastatic parathyroid carcinoma", "Metastatic Parathyroid Carcinoma", "parathyroid carcinoma, metastatic", "Metastatic Parathyroid Gland Cancer", "cancer of the parathyroid, metastatic", "Metastatic Parathyroid Gland Carcinoma", "carcinoma of the parathyroid, metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Parathyroid Gland Carcinoma", "shortest_name_length": 29}
{"curie": "UMLS:C4704742", "names": ["Craniofacial Fibrous Dysplasia", "Craniofacial Fibrous Dysplasias", "Fibrous Dysplasia, Craniofacial", "Craniomaxillofacial Fibrous Dysplasia", "Fibrous Dysplasia, Craniomaxillofacial", "Craniomaxillofacial Fibrous Dysplasias"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Craniofacial Fibrous Dysplasia", "shortest_name_length": 30}
{"curie": "UMLS:C0396006", "names": ["pharynx; stricture", "stricture; pharynx", "pharyngeal stenosis", "Pharyngeal stenosis", "Pharyngeal Stenosis", "Pharyngeal stricture", "Pharyngeal stenosis (disorder)", "pharyngeal stenosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pharyngeal Stenosis", "shortest_name_length": 18}
{"curie": "UMLS:C0854979", "names": ["Stage I Large Cell Lung Cancer", "Large cell lung cancer stage I", "Stage I Large Cell Lung Carcinoma", "Stage I Large Cell Carcinoma of Lung", "Stage I Large Cell Carcinoma of the Lung", "Stage I Lung Large Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Large cell lung cancer stage I", "shortest_name_length": 30}
{"curie": "UMLS:C0543478", "names": ["Residual tumor", "Residual Tumor", "residual tumor", "Residual tumour", "Residual Tumour", "Residual Tumors", "residual_disease", "Residual Disease", "residual disease", "Tumour, Residual", "Residual Tumours"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Residual Tumor", "shortest_name_length": 14}
{"curie": "UMLS:C1335459", "names": ["Stage II Hepatoblastoma", "Postsurgical Stage II Hepatoblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postsurgical Stage II Hepatoblastoma", "shortest_name_length": 23}
{"curie": "UMLS:C0221030", "names": ["Reimann's syndrome", "HYPERVISCOSITY SYNDROME", "Hyperviscosity syndrome", "hyperviscosity syndrome", "hyperviscosity syndromes", "Hyperviscosity syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyperviscosity syndrome", "shortest_name_length": 18}
{"curie": "MONDO:0014863", "names": ["MDFPMR", "macrocephaly, dysmorphic facies, and psychomotor retardation", "MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION", "macrocephaly, dysmorphic facies, and psychomotor retardation; MDFPMR"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macrocephaly, dysmorphic facies, and psychomotor retardation", "shortest_name_length": 6}
{"curie": "UMLS:C4683574", "names": ["Lugano Classification Adult Non-Hodgkin Lymphoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Adult Non-Hodgkin Lymphoma by AJCC v8 Stage", "shortest_name_length": 65}
{"curie": "UMLS:C1698669", "names": ["superficial soft tissue fibrosis", "Superficial soft tissue fibrosis", "Superficial Soft Tissue Fibrosis", "superficial soft tissue fibrosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Superficial Soft Tissue Fibrosis", "shortest_name_length": 32}
{"curie": "UMLS:C4721794", "names": ["Ovarian Cancer Stage IIIA", "Stage IIIA Ovarian Cancer", "FIGO Stage IIIA Ovarian Cancer", "AJCC Stage IIIA Ovarian Cancer", "FIGO Stage IIIA Cancer of Ovary", "Stage IIIA Ovarian Cancer AJCC v6", "FIGO Stage IIIA Ovarian Carcinoma", "Stage IIIA Ovarian Cancer AJCC v7", "FIGO Stage IIIA Carcinoma of Ovary", "FIGO Stage IIIA Cancer of the Ovary", "Stage IIIA Ovarian Epithelial Cancer", "FIGO Stage IIIA Carcinoma of the Ovary", "Stage IIIA Ovarian Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Ovarian Cancer AJCC v6 and v7", "shortest_name_length": 25}
{"curie": "UMLS:C1709158", "names": ["Neonatal Hearing Impairment", "Neonatal hearing impairment"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neonatal hearing impairment", "shortest_name_length": 27}
{"curie": "UMLS:C0353676", "names": ["organophosphorus poisoning", "Organophosphorus Poisoning"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Organophosphorus Poisoning", "shortest_name_length": 26}
{"curie": "UMLS:C0686483", "names": ["lacrimal gland neoplasm malignant secondary", "Secondary malignant neoplasm of lacrimal gland", "Metastatic malignant neoplasm to lacrimal gland", "Metastatic malignant neoplasm of lacrimal gland", "Metastatic Malignant Neoplasm in the Lacrimal Gland", "Metastatic malignant neoplasm to lacrimal gland (disorder)", "Secondary malignant neoplasm of lacrimal gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to lacrimal gland", "shortest_name_length": 43}
{"curie": "MONDO:0010826", "names": ["pyknolepsy", "Pyknolepsy", "Pyknolepsies", "PYKNOEPILEPSY", "Pykno-epilepsy", "pykno-epilepsy", "Pykno Epilepsy", "Pykno-Epilepsy", "absence seizure", "petit mal seizure", "Petit-mal epilepsy", "childhood absence seizure", "Childhood absence seizures", "Childhood Absence Epilepsy", "Childhood absence epilepsy", "childhood absence epilepsy", "Epilepsy, Childhood Absence", "Absence Epilepsy, Childhood", "Childhood absence epilepsy (disorder)", "childhood absence seizure (diagnosis)", "Childhood - juvenile - absence epilepsy", "epilepsy generalized nonconvulsive pykno-epilepsy", "epilepsy generalized nonconvulsive pykno-epilepsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood absence epilepsy", "shortest_name_length": 10}
{"curie": "MONDO:0006360", "names": ["cancer penis", "penile cancer", "Penile Cancer", "carcinoma penis", "Penis carcinoma", "penis carcinoma", "cancer of penis", "Cancer of Penis", "Penile carcinoma", "penile carcinoma", "Penile Carcinoma", "carcinoma of penis", "Carcinoma of Penis", "Penile cancer, NOS", "Carcinoma of penis", "cancer of the penis", "Penis carcinoma NOS", "Cancer of the Penis", "penile cancer, adult", "Carcinoma of the Penis", "carcinoma of the penis", "Carcinoma of penis (disorder)", "carcinoma of penis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "penile carcinoma", "shortest_name_length": 12}
{"curie": "MONDO:0022875", "names": ["cortada Koussef Matsumoto syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cortada Koussef Matsumoto syndrome", "shortest_name_length": 34}
{"curie": "MONDO:0018329", "names": ["persistent combined dystonia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "persistent combined dystonia", "shortest_name_length": 28}
{"curie": "MONDO:0004413", "names": ["Squamous Cell Carcinoma, Non-Keratinizing", "Cervical Non-Keratinizing Squamous Cell Carcinoma", "cervical non-keratinizing squamous cell carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical non-keratinizing squamous cell carcinoma", "shortest_name_length": 41}
{"curie": "UMLS:C4524644", "names": ["Esophageal Squamous Cell Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Squamous Cell Carcinoma by AJCC v8 Stage", "shortest_name_length": 51}
{"curie": "MONDO:0002073", "names": ["pineal cell tumor", "pineal cell tumour", "pineal germ cell tumor", "Pineal germ cell tumor", "Pineal Germ Cell Tumor", "Pineal germ cell tumour", "pineal region germinoma", "Pineal Germ Cell Neoplasm", "Pineal Area Germ Cell Tumor", "Pineal Region germ cell tumor", "pineal region germ cell tumor", "Pineal Region Germ Cell Tumor", "Pineal Area Germ Cell Neoplasm", "Pineal Region Germ Cell Neoplasm", "Pineal germ cell tumor (disorder)", "Pineal germ cell tumor (diagnosis)", "pineal germ cell neoplasm, malignant", "Pineal Germ Cell Neoplasm, Malignant", "Malignant Pineal Area Germ Cell Tumor", "malignant pineal area germ cell tumor", "Malignant Pineal Gland Germ Cell Tumor", "malignant pineal gland germ cell tumor", "Malignant Pineal Region Germ Cell Tumor", "malignant pineal region germ cell tumor", "Malignant Pineal Area Germ Cell Neoplasm", "malignant pineal area germ cell neoplasm", "malignant pineal gland germ cell neoplasm", "Malignant Pineal Gland Germ Cell Neoplasm", "Malignant Germ Cell Tumor of Pineal Gland", "malignant germ cell tumor of pineal gland", "Malignant Pineal Region Germ Cell Neoplasm", "malignant pineal region germ cell neoplasm", "Malignant Germ Cell Neoplasm of Pineal Gland", "malignant germ cell neoplasm of pineal gland", "Malignant Pineal Parenchymal Germ Cell Tumor", "malignant Pineal Parenchymal germ cell tumor", "malignant pineal parenchymal germ cell tumor", "Malignant Germ Cell Tumor of the Pineal Gland", "malignant germ cell tumor of the pineal gland", "Malignant Germ Cell Tumor of Pineal Parenchyma", "malignant germ cell tumor of pineal parenchyma", "Malignant Pineal Parenchymal Germ Cell Neoplasm", "malignant pineal parenchymal germ cell neoplasm", "Malignant Germ Cell Neoplasm of the Pineal Gland", "malignant germ cell neoplasm of the pineal gland", "malignant germ cell neoplasm of pineal parenchyma", "Malignant Germ Cell Neoplasm of Pineal Parenchyma", "Malignant Germ Cell Tumor of the Pineal Parenchyma", "malignant germ cell tumor of the pineal parenchyma", "neoplasm of endocrine gland pineal germ cell tumor", "Malignant Germ Cell Neoplasm of the Pineal Parenchyma", "malignant germ cell neoplasm of the pineal parenchyma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant pineal area germ cell neoplasm", "shortest_name_length": 17}
{"curie": "UMLS:C0796292", "names": ["Stage II Immunoblastic Lymphoma", "stage II adult contiguous immunoblastic lymphoma", "Stage II Adult Contiguous Immunoblastic Lymphoma", "Ann Arbor Stage II Adult Contiguous Immunoblastic Lymphoma", "Contiguous Adult Immunoblastic Large Cell Lymphoma Stage II", "contiguous stage II adult immunoblastic large cell lymphoma", "Stage II Contiguous Adult Immunoblastic Large Cell Lymphoma", "contiguous adult immunoblastic large cell lymphoma stage II", "Contiguous Stage II Adult Immunoblastic Large Cell Lymphoma", "stage II contiguous adult immunoblastic large cell lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage II Adult Contiguous Immunoblastic Lymphoma", "shortest_name_length": 31}
{"curie": "UMLS:C4525128", "names": ["Stage IV Colon Cancer", "Stage IV Colon Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Colon Cancer AJCC v8", "shortest_name_length": 21}
{"curie": "MONDO:0009080", "names": ["SHFM1D", "Split hand-split foot-deafness syndrome", "split hand-split foot-deafness syndrome", "Split hand-split foot-hearing loss syndrome", "Congenital deafness with split hands and feet", "congenital deafness with split hands and feet", "Deafness, Congenital, And Split Hands And Feet", "DEAFNESS, CONGENITAL, WITH SPLIT HANDS AND FEET", "deafness, congenital, with split hands and feet", "Split-Hand-Foot Malformation With Sensorineural Hearing Loss", "split-hand/foot malformation 1 with sensorineural hearing loss", "split hand-foot malformation 1 with sensorineural hearing loss", "Split hand, split foot malformation with sensorineural hearing loss syndrome", "split-hand/foot malformation 1 with sensorineural hearing loss, autosomal recessive", "SPLIT-HAND/FOOT MALFORMATION 1 WITH SENSORINEURAL HEARING LOSS, AUTOSOMAL RECESSIVE", "Split hand, split foot malformation with sensorineural hearing loss syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "split hand-foot malformation 1 with sensorineural hearing loss", "shortest_name_length": 6}
{"curie": "MONDO:0006104", "names": ["benign chemodectoma", "Benign Chemodectoma", "CHEMODECTOMA, BENIGN", "chemodectoma, benign", "benign carotid body paraganglioma", "Benign Carotid Body Paraganglioma", "carotid body paraganglioma, benign", "Non-Metastatic Carotid Body Paraganglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign carotid body paraganglioma", "shortest_name_length": 19}
{"curie": "MONDO:0025457", "names": ["Jagziekte", "Jaagziekte", "Jaagsiekte", "Lunger disease", "Jaagziekte (disorder)", "Ovine pulmonary carcinoma", "Ovine Pulmonary Carcinoma", "Ovine pulmonary carcinomas", "Ovine Pulmonary Carcinomas", "Carcinoma, Ovine Pulmonary", "carcinoma, Ovine pulmonary", "Pulmonary Carcinoma, Ovine", "pulmonary carcinoma, Ovine", "Pulmonary Carcinomas, Ovine", "Carcinomas, Ovine Pulmonary", "pulmonary carcinomas, Ovine", "carcinomas, Ovine pulmonary", "Pulmonary Ovine Adenomatoses", "Ovine pulmonary Adenomatoses", "Pulmonary Ovine Adenomatosis", "pulmonary Ovine Adenomatoses", "Ovine Pulmonary Adenomatosis", "pulmonary Ovine adenomatosis", "Ovine Pulmonary Adenomatoses", "Ovine pulmonary adenomatosis", "Ovine Adenomatosis, Pulmonary", "Adenomatosis, Pulmonary Ovine", "pulmonary adenomatosis, ovine", "Ovine Adenomatoses, Pulmonary", "Pulmonary Adenomatoses, Ovine", "Pulmonary Adenomatosis, Ovine", "Adenomatoses, Pulmonary Ovine", "pulmonary Adenomatoses, Ovine", "Ovine adenomatosis, pulmonary", "Adenomatoses, Ovine pulmonary", "adenomatosis, pulmonary Ovine", "adenomatosis, Ovine pulmonary", "Adenomatoses, pulmonary Ovine", "Adenomatoses, Ovine Pulmonary", "Ovine Adenomatoses, pulmonary", "Adenomatosis, Ovine Pulmonary", "Adenomatosis, Pulmonary, Ovine", "adenomatosis, pulmonary, Ovine", "Pulmonary adenomatosis of sheep"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary adenomatosis, ovine", "shortest_name_length": 9}
{"curie": "MONDO:0015085", "names": ["BSI", "Bathing suit ichthyosis", "bathing suit ichthyosis", "Bathing suit ichthyosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bathing suit ichthyosis", "shortest_name_length": 3}
{"curie": "UMLS:C0206019", "names": ["HIV encephalitis", "encephalitis HIV", "HIV encephalopathy", "HIV Encephalopathy", "Encephalopathy, HIV", "AIDS encephalopathy", "AIDS ENCEPHALOPATHY", "AIDS Encephalopathy", "HIV Encephalopathies", "Encephalopathy, AIDS", "Encephalopathies, HIV", "AIDS Encephalopathies", "Encephalopathies, AIDS", "AIDS with encephalopathy", "HIV disease; encephalopathy", "HIV encephalopathy (diagnosis)", "HIV disease resulting in encephalopathy", "HIV disease; resulting in, encephalopathy", "encephalopathy; resulting from HIV disease", "Human immunodeficiency virus encephalopathy", "Human immunodeficiency virus encephalopathy (disorder)", "Encephalopathy with acquired immunodeficiency syndrome", "acquired immunodeficiency syndrome (AIDS) encephalopathy", "Encephalopathy with AIDS (acquired immunodeficiency syndrome)", "Encephalopathy with acquired immunodeficiency syndrome (disorder)", "acquired immunodeficiency syndrome (AIDS) encephalopathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HIV Encephalopathy", "shortest_name_length": 16}
{"curie": "MONDO:0002277", "names": ["ASCVD", "ascvd", "ATHEROSCLEROSIS", "arteriosclerosis", "Arteriosclerosis", "ARTERIOSCLEROSIS", "Arterioscleroses", "arterioscleroses", "Vascular sclerosis", "Arterial Sclerosis", "VASCULAR SCLEROSES", "arterial sclerosis", "Vascular Sclerosis", "vascular sclerosis", "Hardened artery wall", "Arteriosclerosis, NOS", "arteriovascular disease", "arteriosclerosis disorder", "arteriosclerotic CV disease", "arteriosclerosis cardiovascular", "cardiovascular arteriosclerosis", "Cardiovascular arteriosclerosis", "arteriosclerosis; cardiovascular", "cardiovascular; arteriosclerosis", "arteriosclerotic vascular disease", "ARTERIOSCLEROTIC VASCULAR DISEASE", "Arteriosclerosis/ Atherosclerosis", "Arteriosclerotic vascular disease", "Arteriosclerotic vascular disease NOS", "Arteriosclerotic vascular disease, NOS", "Arteriosclerotic cardiovascular disease", "arteriosclerotic cardiovascular disease", "Arteriosclerotic Cardiovascular Disease", "Arteriosclerosis (morphologic abnormality)", "Vascular sclerosis (morphologic abnormality)", "Arteriosclerotic vascular disease (disorder)", "Arteriosclerotic cardiovascular disease, NOS", "Cardiovascular disease with arteriosclerosis", "arteriosclerotic vascular disease (diagnosis)", "Cardiovascular sclerosis with arteriosclerosis", "arteriosclerotic cardiovascular disease (ASCVD)", "ASCVD (arteriosclerotic cardiovascular disease)", "Cardiovascular degeneration with arteriosclerosis", "disease (or disorder); arteriosclerotic, cardiovascular", "arteriosclerotic cardiovascular disease (ASCVD) (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arteriosclerosis disorder", "shortest_name_length": 5}
{"curie": "UMLS:C4744674", "names": ["Refractory Aggressive Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Aggressive Non-Hodgkin Lymphoma", "shortest_name_length": 42}
{"curie": "MONDO:0020240", "names": ["syndromic retinitis pigmentosa", "syndrome associated with retinitis pigmentosa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic retinitis pigmentosa", "shortest_name_length": 30}
{"curie": "UMLS:C1112427", "names": ["Bursa injury", "Bursa Injury", "bursa injury", "bursa injuries"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bursa injury", "shortest_name_length": 12}
{"curie": "UMLS:C4725870", "names": ["Resectable Undifferentiated Pleomorphic Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Undifferentiated Pleomorphic Sarcoma", "shortest_name_length": 47}
{"curie": "UMLS:C0751784", "names": ["Late Onset Lafora Body Disease", "Lafora-Body Disease, Late Onset", "Lafora Body Disease, Late Onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lafora Body Disease, Late Onset", "shortest_name_length": 30}
{"curie": "MONDO:0005510", "names": ["hydronephrosis", "hydronephroses", "Hydronephrosis", "HYDRONEPHROSIS", "Hydronephroses", "Hydronephrosis (disorder)", "hydronephrosis (diagnosis)", "Unspecified hydronephrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hydronephrosis", "shortest_name_length": 14}
{"curie": "MONDO:0012862", "names": ["ADHD5", "MOTOR TIMING QUANTITATIVE TRAIT LOCUS", "motor timing quantitative trait locus", "ATTENTION DEFICIT-HYPERACTIVITY DISORDER, SUSCEPTIBILITY TO, 5", "attention deficit-hyperactivity disorder, susceptibility to, 5", "attention Deficit-hyperactivity disorder, susceptibility to, type 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "attention deficit-hyperactivity disorder, susceptibility to, 5", "shortest_name_length": 5}
{"curie": "MONDO:0017316", "names": ["thong-Douglas-Ferrante syndrome", "thong Douglas Ferrante syndrome", "Thong-Douglas-Ferrante syndrome", "Thong Douglas Ferrante syndrome", "short stature deafness neutrophil dysfunction", "short stature-deafness-neutrophil dysfunction-dysmorphism syndrome", "Short stature-deafness-neutrophil dysfunction-dysmorphism syndrome", "Short stature-hearing loss-neutrophil dysfunction-dysmorphism syndrome", "Short stature and deafness with neutrophil dysfunction and facial dysmorphism syndrome", "Short stature and deafness with neutrophil dysfunction and facial dysmorphism syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short stature-deafness-neutrophil dysfunction-dysmorphism syndrome", "shortest_name_length": 31}
{"curie": "MONDO:0018912", "names": ["CUSHING", "cortisol Excess", "Itsenko disease", "Cortisol Excess", "CUSHING SYNDROME", "cushing syndrome", "Cushing syndrome", "Cushing Syndrome", "hypercortisolism", "Hypercortisolism", "Cushings Syndrome", "cushings syndrome", "Cushings syndrome", "Syndrome, Cushing", "CUSHINGS SYNDROME", "cushing's syndrome", "Cushing's syndrome", "CUSHING'S SYNDROME", "Syndrome Cushing's", "SYNDROME CUSHING'S", "Cushing's Syndrome", "Syndrome, Cushing's", "Hyperadrenocorticism", "hyperadrenocorticism", "pituitary basophilism", "Cushing's basophilism", "Cushing's syndrome NOS", "Cushing's syndrome III", "suprarenogenic syndrome", "Suprarenogenic syndrome", "Itsenko-Cushing syndrome", "Cushing; syndrome or disease", "Cushing's syndrome (diagnosis)", "Cushing's syndrome, unspecified", "nodular primary adrenocortical dysplasia", "ectopic adrenocorticotropic hormone syndrome", "adrenal hyperfunction resulting from pituitary ACTH excess"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cushing syndrome", "shortest_name_length": 7}
{"curie": "MONDO:0020108", "names": ["AHA", "AIHA", "immunohemolytic anemia", "immuno-hemolytic anemia", "Anemia hemolytic autoimmune", "Autoimmune hemolytic anemia", "ANEMIA HEMOLYTIC AUTOIMMUNE", "autoimmune hemolytic anemia", "Autoimmune Hemolytic Anemia", "anemia autoimmune hemolytic", "anemia hemolytic autoimmune", "hemolytic autoimmune anemia", "Autoimmune hemolytic anemias", "Hemolytic anemia, autoimmune", "anemia, autoimmune hemolytic", "Autoimmune Hemolytic Anemias", "Anemia, Autoimmune Hemolytic", "Hemolytic anemia, Autoimmune", "Autoimmune hemolytic anaemia", "Hemolytic Anemia, Autoimmune", "autoimmune hemolytic anemias", "autoimmune hemolytic anaemia", "ANEMIA, AUTOIMMUNE HEMOLYTIC", "Autoimmune Haemolytic Anaemia", "Autoimmune haemolytic anaemia", "hemolytic; anemia, autoimmune", "anemia; hemolytic, autoimmune", "anaemia haemolytic autoimmune", "Anaemia haemolytic autoimmune", "Anemia, Hemolytic, Autoimmune", "autoimmune haemolytic anaemia", "Anaemia, Autoimmune Haemolytic", "Haemolytic Anaemia, Autoimmune", "Autoimmune Haemolytic Anaemias", "autoimmune haemolytic anaemias", "Autoimmune hemolytic anemia NOS", "Immune mediated hemolytic anemia", "Autoimmune hemolytic anemia, NOS", "Anemia hemolytic autoimmune (NOS)", "ANEMIA HEMOLYTIC AUTOIMMUNE (NOS)", "Autoimmune haemolytic anaemia NOS", "AIHA - Autoimmune hemolytic anemia", "Autoimmune haemolytic anaemia, NOS", "anemia hemolytic acquired autoimmune", "acquired autoimmune hemolytic anemia", "AIHA - Autoimmune haemolytic anaemia", "Hemolytic anemia due to antibody, NOS", "Autoimmune hemolytic anemia (disorder)", "idiopathic autoimmune hemolytic anemia", "Autoimmune hemolytic anemia (diagnosis)", "Haemolytic anaemia due to antibody, NOS", "familial auto-immune hemolytic anemia (subtype)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune hemolytic anemia", "shortest_name_length": 3}
{"curie": "MONDO:0012706", "names": ["ETL4", "EPOLM", "familial temporal lobe epilepsy 4", "EPILEPSY, FAMILIAL TEMPORAL LOBE, 4", "epilepsy, familial temporal lobe, 4", "Epilepsy, Familial Temporal Lobe, 4", "familial temporal lobe epilepsy type 4", "occipitotemporal lobe epilepsy and migraine with aura", "epilepsy, occipitotemporal lobe, and migraine with aura", "EPILEPSY, OCCIPITOTEMPORAL LOBE, AND MIGRAINE WITH AURA", "Epilepsy, Occipitotemporal Lobe, And Migraine With Aura"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial temporal lobe epilepsy 4", "shortest_name_length": 4}
{"curie": "UMLS:C1533649", "names": ["Renal AVM/H", "Renal Arteriovenous Malformation", "Renal arteriovenous malformation", "Arteriovenous malformation of kidney", "congenital renal arteriovenous malformation", "Renal Arteriovenous Malformation/Hemangioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital renal arteriovenous malformation", "shortest_name_length": 11}
{"curie": "MONDO:0010793", "names": ["Nephropathy, Chronic Tubulointerstitial", "NEPHROPATHY, CHRONIC TUBULOINTERSTITIAL", "nephropathy, chronic tubulointerstitial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephropathy, chronic tubulointerstitial", "shortest_name_length": 39}
{"curie": "MONDO:0009746", "names": ["CIPA", "HSAN4", "HSAN 4", "HSNAN4", "HSAN IV", "HSAN Type IV", "Type IV, HSAN", "CIP-anhidrosis syndrome", "Familial Dysautonomia, Type 2", "familial dysautonomia, type 2", "Familial Dysautonomia, Type II", "FAMILIAL DYSAUTONOMIA, TYPE II", "hereditary sensory neuropathy type 4", "hereditary sensory neuropathy type IV", "Swanson-Buchanan-Alvord neuropathy syndrome", "hereditary sensory and autonomic neuropathy 4", "Congenital sensory neuropathy with anhidrosis", "Hereditary Sensory and Autonomic Neuropathy 4", "Pain Insensitivity with Anhidrosis, Congenital", "HEREDITARY SENSORY AND AUTONOMIC NEUROPATHY IV", "Hereditary Sensory And Autonomic Neuropathy IV", "neuropathy, congenital sensory, with anhidrosis", "Neuropathy, Congenital Sensory, with Anhidrosis", "Hereditary Sensory Autonomic Neuropathy, Type 4", "NEUROPATHY, CONGENITAL SENSORY, WITH ANHIDROSIS", "congenital insensitivity to pain with anhidrosis", "Hereditary sensory neuropathy, type 4, recessive", "Congenital insensitivity to pain with anhidrosis", "Congenital Insensitivity to Pain with Anhidrosis", "Hereditary insensitivity to pain with anhidrosis", "Recessive hereditary sensory neuropathy, type IV", "Insensitivity to Pain with Anhidrosis, Congenital", "NTRK1 hereditary sensory and autonomic neuropathy", "Autosomal recessive hereditary sensory neuropathy", "insensitivity to pain, congenital, with anhidrosis", "INSENSITIVITY TO PAIN, CONGENITAL, WITH ANHIDROSIS", "hereditary sensory and autonomic neuropathy type 4", "Insensitivity to Pain, Congenital, with Anhidrosis", "Hereditary sensory and autonomic neuropathy type 4", "Hereditary Sensory and Autonomic Neuropathy, Type 4", "Hereditary Sensory and Autonomic Neuropathy Type IV", "hereditary sensory and autonomic neuropathy type IV", "Hereditary sensory and autonomic neuropathy type IV", "Hereditary sensory and autonomic neuropathy, type IV", "congenital insensitivity to pain-anhidrosis syndrome", "Neuropathy, Hereditary Sensory and Autonomic, Type IV", "Hereditary insensitivity to pain with anhidrosis (disorder)", "Congenital insensitivity to pain, anhidrosis and mental retardation", "hereditary sensory and autonomic neuropathy caused by mutation in NTRK1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary sensory and autonomic neuropathy type 4", "shortest_name_length": 4}
{"curie": "UMLS:C2347753", "names": ["Pure Erythroid Leukemia", "adult pure erythroid leukemia", "Adult Pure Erythroid Leukemia", "adult pure erythroid leukemia (M6b)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Pure Erythroid Leukemia", "shortest_name_length": 23}
{"curie": "UMLS:C0855260", "names": ["Jealous Type Delusional Disorder", "Delusional disorder, jealous type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Delusional disorder, jealous type", "shortest_name_length": 32}
{"curie": "MONDO:0010177", "names": ["Vascular hyalinosis", "vascular hyalinosis", "Vascular Hyalinosis", "VASCULAR HYALINOSIS", "Rambaud-Gallian syndrome", "Rambaud-Gallian-Touchard syndrome", "retinal ischemic syndrome-digestive tract small vessel hyalinosis-diffuse cerebral calcifications syndrome", "digestive tract and renal small vessel hyalinosis, intracerebral calcifications, retinal ischemic syndrome and phenotypic a"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vascular hyalinosis", "shortest_name_length": 19}
{"curie": "UMLS:C4684820", "names": ["Thoracic NMC", "Thoracic NUT Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thoracic NUT Carcinoma", "shortest_name_length": 12}
{"curie": "MONDO:0007440", "names": ["MD1", "BPAD", "MAFD1", "MANIC-DEPRESSIVE PSYCHOSIS", "MAJOR affective disorder 1", "major affective disorder 1", "Major Affective Disorder 1", "BIPOLAR AFFECTIVE DISORDER", "MAJOR AFFECTIVE DISORDER 1", "manic-depressive psychosis", "bipolar affective disorder", "MANIC-DEPRESSIVE PSYCHOSIS, AUTOSOMAL", "manic-depressive psychosis, autosomal", "Manic-Depressive Psychosis, Autosomal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "major affective disorder 1", "shortest_name_length": 3}
{"curie": "MONDO:0009604", "names": ["NADH-CYB5R Deficiency", "NADPH-reductase deficiency", "Methemoglobin reductase deficiency", "Methemoglobin Reductase Deficiency", "METHEMOGLOBIN REDUCTASE DEFICIENCY", "methemoglobin reductase deficiency", "Cytochrome B5 Reductase Deficiency", "Methaemoglobin reductase deficiency", "NADH-Cytochrome B5 Reductase Deficiency", "TPNH-Methemoglobin Reductase Deficiency", "TPNH-methemoglobin reductase deficiency", "TPNH-METHEMOGLOBIN REDUCTASE DEFICIENCY", "NADH-methemoglobin reductase deficiency disease", "NADH-Dependent Methemoglobin Reductase Deficiency", "NADPH-Dependent Methemoglobin Reductase Deficiency", "NADPH-dependent methemoglobin reductase deficiency", "NADPH-DEPENDENT METHEMOGLOBIN REDUCTASE DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "methemoglobin reductase deficiency", "shortest_name_length": 21}
{"curie": "UMLS:C0796612", "names": ["Recurrent Ependymoma", "Relapsed Childhood Ependymoma", "Relapsed Pediatric Ependymoma", "Recurrent Pediatric Ependymoma", "Recurrent Childhood Ependymoma", "recurrent childhood ependymoma", "ependymoma, recurrent childhood", "childhood ependymoma, recurrent", "ependymoma, childhood, recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Ependymoma", "shortest_name_length": 20}
{"curie": "MONDO:0010478", "names": ["CDG2M", "DEE22", "CDGIIm", "EIEE22", "CDG-IIm", "CDG IIm", "SLC35A2-CDG", "CDG syndrome type IIm", "SLC35A2-congenital disorder of glycosylation", "Congenital disorder of glycosylation type 2m", "congenital disorder of glycosylation type 2m", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 22", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 22", "congenital disorder of glycosylation type IIm", "epileptic encephalopathy, early infantile, 22", "developmental and epileptic encephalopathy 22", "Congenital disorder of glycosylation type IIm", "congenital disorder of glycosylation, type IIm", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm", "CDG2M - congenital disorder of glycosylation type 2m", "epileptic encephalopathy, early infantile, 22; EIEE22", "Solute carrier family 35 member A2 congenital disorder of glycosylation", "Solute carrier family 35 member A2 congenital disorder of glycosylation (disorder)", "congenital disorder of glycosylation, type IIm, Somatic mosaicism, X-linked dominant", "SLC35A2-CDG - solute carrier family 35 member A2 congenital disorder of glycosylation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SLC35A2-congenital disorder of glycosylation", "shortest_name_length": 5}
{"curie": "MONDO:0000783", "names": ["orange allergy", "Citrus sinensis fruit allergy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orange allergy", "shortest_name_length": 14}
{"curie": "UMLS:C5669920", "names": ["Infant-Type Hemispheric Glioma, NTRK-Altered"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infant-Type Hemispheric Glioma, NTRK-Altered", "shortest_name_length": 44}
{"curie": "MONDO:0016116", "names": ["generalized bulbospinal muscular atrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "generalized bulbospinal muscular atrophy", "shortest_name_length": 40}
{"curie": "MONDO:0002644", "names": ["granulomatous myositis", "Idiopathic Granulomatous Myositis", "idiopathic granulomatous myositis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic granulomatous myositis", "shortest_name_length": 22}
{"curie": "UMLS:C0522616", "names": ["Atypical apocrine metaplasia", "Atypical Apocrine Metaplasia", "Atypical apocrine metaplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atypical apocrine metaplasia", "shortest_name_length": 28}
{"curie": "UMLS:C1883424", "names": ["Carcinoma with osteoclast-like giant cells", "Undifferentiated Carcinoma with Osteoclast-Like Giant Cells"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Undifferentiated Carcinoma with Osteoclast-Like Giant Cells", "shortest_name_length": 42}
{"curie": "UMLS:C4521724", "names": ["Stage I Esophageal Squamous Cell Cancer", "Clinical Stage I Esophageal Squamous Cell Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage I Esophageal Squamous Cell Carcinoma AJCC v8", "shortest_name_length": 39}
{"curie": "UMLS:C2981717", "names": ["stage IIB mycosis fungoides/Sezary syndrome", "Stage IIB Mycosis Fungoides and Sézary Syndrome", "Stage IIB Mycosis Fungoides and Sezary Syndrome", "Stage IIB Mycosis Fungoides and Sezary Syndrome AJCC v7", "stage IIB mycosis fungoides and Sezary syndrome AJCC v7", "Stage IIB Mycosis Fungoides and Sézary Syndrome AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Mycosis Fungoides and Sezary Syndrome AJCC v7", "shortest_name_length": 43}
{"curie": "MONDO:0019015", "names": ["Amniocele", "exomphalos", "Exomphalos", "eventration", "omphalocele", "Eventration", "OMPHALOCELE", "Omphalocele", "omphalocoele", "Omphalocoele", "omphaloceles", "Omphaloceles", "omphalocele (___ cm)", "omphalocele (disease)", "Congenital omphalocele", "Congenital Omphalocele", "congenital omphalocele", "omphalocele (diagnosis)", "abdomen omphalocele (___ cm)", "omphalocele (physical finding)", "Congenital omphalocele (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "omphalocele", "shortest_name_length": 9}
{"curie": "MONDO:0011867", "names": ["microphthalmia with cyst, bilateral facial clefts, and limb anomalies", "Microphthalmia with Cyst, Bilateral Facial Clefts, and Limb Anomalies", "MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microphthalmia with cyst, bilateral facial clefts, and limb anomalies", "shortest_name_length": 69}
{"curie": "UMLS:C0751640", "names": ["Cryptogenic Partial Complex Epilepsy", "Partial Complex Epilepsy, Cryptogenic", "Epilepsy, Cryptogenic, Partial Complex"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cryptogenic Partial Complex Epilepsy", "shortest_name_length": 36}
{"curie": "MONDO:0030716", "names": ["SPGF66", "spermatogenic failure 66", "SPERMATOGENIC FAILURE 66"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 66", "shortest_name_length": 6}
{"curie": "MONDO:0018537", "names": ["Squamous cell carcinoma of gallblader and EBT", "squamous cell carcinoma of gallblader and EBT", "Squamous cell carcinoma of gallbladder and extrahepatic biliary tract", "squamous cell carcinoma of gallbladder and extrahepatic biliary tract", "Squamous cell carcinoma of gallbladder and extrahepatic biliary tract (disorder)", "squamous cell carcinoma of gallbladder and extrahepatic biliary tract (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "squamous cell carcinoma of gallbladder and extrahepatic biliary tract", "shortest_name_length": 45}
{"curie": "UMLS:C1335904", "names": ["Salivary Gland Myoepithelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Salivary Gland Myoepithelial Carcinoma", "shortest_name_length": 38}
{"curie": "UMLS:C1708896", "names": ["Malignant Outer Hair Sheath and Infundibulum Tumor", "Malignant Outer Hair Sheath and Infundibulum Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Outer Hair Sheath and Infundibulum Neoplasm", "shortest_name_length": 50}
{"curie": "MONDO:0009197", "names": ["tec", "TEC", "erythroblastopenia, transient", "Erythroblastopenia, transient", "ERYTHROBLASTOPENIA, TRANSIENT", "transient erythrocytopenia of childhood", "Transient acquired pure red cell aplasia", "transient acquired pure red cell aplasia", "Transient Erythroblastopenia of Childhood", "transient erythroblastopenia of childhood", "TRANSIENT ERYTHROBLASTOPENIA OF CHILDHOOD", "Transient erythroblastopenia of childhood", "red blood cell aplasia acquired transient pure", "transient acquired pure red blood cell aplasia", "TEC - Transient erythroblastopenia of childhood", "Familial transient erythroblastopenia of childhood", "familial transient erythroblastopenia of childhood", "Transient acquired pure red cell aplasia (disorder)", "transient erythrocytopenia of childhood (diagnosis)", "Transient erythroblastopenia of childhood (disorder)", "transient acquired pure red blood cell aplasia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transient erythroblastopenia of childhood", "shortest_name_length": 3}
{"curie": "MONDO:0005468", "names": ["LBP", "Low BP", "low bp", "BP fell", "bp lower", "BP lowered", "Hypopiesis", "hypopiesis", "hypotension", "Hypotension", "HYPOTENSION", "Hypotension NOS", "Hypotension, NOS", "Blood pressure low", "Low Blood Pressure", "BLOOD PRESSURE LOW", "Low;blood pressure", "low blood pressure", "Low blood pressure", "blood pressure low", "blood drop pressure", "Blood Pressure, Low", "low; blood pressure", "blood pressure drop", "blood pressure; low", "low blood pressures", "arterial hypotension", "hypotension arterial", "blood pressure lower", "Systemic hypotension", "Vascular Hypotension", "hypotensive disorder", "HYPOTENSIVE DISEASES", "blood drops pressure", "lower blood pressure", "blood falls pressure", "Arterial hypotension", "hypotension (disease)", "blood lowing pressure", "blood lowers pressure", "Hypotension, Vascular", "drop in blood pressure", "blood falling pressure", "dropped blood pressure", "Drop in blood pressure", "Drop of blood pressure", "Blood pressure dropped", "Lowered blood pressure", "Fall in blood pressure", "blood lowered pressure", "hypotension (diagnosis)", "blood dropping pressure", "Decreased blood pressure", "Arterial hypotension NOS", "Blood pressure decreased", "Hypotension, unspecified", "hypotension was observed", "decreased blood pressure", "BLOOD PRESSURE DECREASED", "decreased; blood pressure", "blood decreasing pressure", "Arterial hypotension, NOS", "blood pressure; decreased", "Decrease in blood pressure", "PRESSURE ARTERIAL DECREASED", "Pressure arterial decreased", "BLOOD PRESSURE DROP ARTERIAL", "Blood pressure drop arterial", "Vascular Hypotensive Disorder", "Low blood pressure (disorder)", "hypotension (physical finding)", "Low Blood Pressure/ Hypotension", "Arterial pressure NOS decreased", "ARTERIAL BLOOD PRESSURE DECREASED", "Arterial blood pressure decreased"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotensive disorder", "shortest_name_length": 3}
{"curie": "UMLS:C5446922", "names": ["Encapsulated Breast Papillary Carcinoma with Invasion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Encapsulated Breast Papillary Carcinoma with Invasion", "shortest_name_length": 53}
{"curie": "MONDO:0005146", "names": ["PTSD", "combat fatigue", "Combat Neurosis", "combat neurosis", "traumatic neurosis", "Traumatic Neurosis", "Traumatic neuroses", "Traumatic neurosis", "Neurosis, traumatic", "traumatic; neurosis", "neurosis; traumatic", "Posttraumatic Neuroses", "Post-Traumatic Neuroses", "Neuroses, Posttraumatic", "Neuroses, Post Traumatic", "Neuroses, Post-Traumatic", "Posttraumatic stress symptom", "Posttraumatic Stress Disorder", "Posttraumatic stress disorder", "posttraumatic stress disorder", "Post-traumatic stress disorder", "Post Traumatic Stress Disorder", "post traumatic stress syndrome", "Posttraumatic Stress Disorders", "Post-Traumatic Stress Disorder", "posttraumatic stress disorders", "POST TRAUMATIC STRESS DISORDER", "Disorder;post traumatic stress", "post-traumatic stress disorder", "post traumatic stress disorder", "post-traumatic stress syndrome", "Post-traumatic stress syndrome", "Stress Disorder, Posttraumatic", "disorder, post-traumatic stress", "post-traumatic stress; disorder", "disorder; post-traumatic stress", "Post Traumatic Stress Disorders", "Stress Disorder, Post Traumatic", "post traumatic stress disorders", "post-traumatic stress disorders", "Post-Traumatic Stress Disorders", "Stress Disorders, Posttraumatic", "Stress Disorder, Post-Traumatic", "stress; disorder, post-traumatic", "disorder; stress, post-traumatic", "Stress Disorders, Post-Traumatic", "Posttraumatic stress disorder NOS", "Posttraumatic stress disorder, NOS", "PTSD - Post-traumatic stress disorder", "Post traumatic stress disorder (PTSD)", "post-traumatic stress disorder (PTSD)", "Post-traumatic stress disorder (PTSD)", "Post-Traumatic Stress Disorder (PTSD)", "Posttraumatic stress disorder (disorder)", "post-traumatic stress disorder (diagnosis)", "Post-traumatic stress disorder, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "post-traumatic stress disorder", "shortest_name_length": 4}
{"curie": "MONDO:0018962", "names": ["common mesentery", "universal mesentery", "Universal mesentery", "Universal mesentery (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "common mesentery", "shortest_name_length": 16}
{"curie": "UMLS:C5231080", "names": ["EMPSGC", "Endocrine mucin-producing sweat gland carcinoma", "Endocrine Mucin-Producing Sweat Gland Carcinoma", "Endocrine mucin-producing sweat gland carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endocrine mucin-producing sweat gland carcinoma", "shortest_name_length": 6}
{"curie": "MONDO:0035362", "names": ["TRIM22-related IBD", "TRIM22-related inflammatory bowel disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "TRIM22-related inflammatory bowel disease", "shortest_name_length": 18}
{"curie": "MONDO:0002266", "names": ["Malt fever", "malt worker lung", "malt workers lung", "Maltworker's lung", "maltworker's lung", "Malt workers lung", "lung malt workers", "maltworkers' lung", "Malt-worker's lung", "Malt-workers' lung", "malt worker's lung", "Malt workers' lung", "Malt worker's lung", "Malt-workers' alveolitis", "Malt house workers' cough", "Malt-workers' lung disease", "maltworkers' lung (diagnosis)", "Malt-workers' lung (disorder)", "alveolitis; Aspergillus clavatus", "Aspergillus clavatus; alveolitis", "Alveolitis due to Aspergillus clavatus", "alveolitis due to aspergillus clavatus", "Aspergillus extrinsic allergic alveolitis", "Aspergillus caused extrinsic allergic alveolitis", "Alveolitis due to Aspergillus clavatus and fumigatus", "Alveolitis due to Aspergillus clavatus AND/OR fumigatus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malt worker's lung", "shortest_name_length": 10}
{"curie": "UMLS:C1288351", "names": [], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"]}
{"curie": "MONDO:0017789", "names": ["idiopathic linear interstitial keratitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic linear interstitial keratitis", "shortest_name_length": 40}
{"curie": "UMLS:C0751484", "names": ["Sporadic Retinoblastoma", "Retinoblastoma, Sporadic", "Sporadic Retinoblastomas", "Retinoblastomas, Sporadic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sporadic Retinoblastoma", "shortest_name_length": 23}
{"curie": "MONDO:0013052", "names": ["RP42", "Retinitis Pigmentosa 42", "retinitis pigmentosa 42", "RETINITIS PIGMENTOSA 42", "KLHL7 retinitis pigmentosa", "retinitis pigmentosa type 42", "retinitis pigmentosa caused by mutation in KLHL7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 42", "shortest_name_length": 4}
{"curie": "UMLS:C0346094", "names": ["Common Blue Nevus", "Common Blue Nevus of Skin", "Common blue nevus of skin", "Common blue naevus of skin", "Common Blue Nevus of the Skin", "Common blue nevus of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Common blue nevus of skin", "shortest_name_length": 17}
{"curie": "MONDO:0019321", "names": ["Atypical Werner syndrome", "atypical Werner syndrome", "Atypical progeroid syndrome", "atypical progeroid syndrome", "Atypical Werner syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical Werner syndrome", "shortest_name_length": 24}
{"curie": "MONDO:0006456", "names": ["THYM", "thymoma", "THYMOMA", "Thymoma", "thymomas", "Thymomas", "Thymoma NOS", "Thymoma, NOS", "thymoma (disease)", "Thymoma (disorder)", "thymoma (diagnosis)", "primary thymic epithelial tumor", "Primary thymic epithelial tumor", "Thymoma (morphologic abnormality)", "Primary thymic epithelial neoplasm", "primary thymic epithelial neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thymoma", "shortest_name_length": 4}
{"curie": "MONDO:0002545", "names": ["MYELOPATHY", "Myelopathy", "myelopathy", "myelopathies", "MYELOPATHIES", "Myelopathies", "Myelopathy NOS", "MP - Myelopathy", "Myelopathy, NOS", "Spinal Cord Disease", "SPINAL CORD DISEASE", "Spinal cord disease", "spinal cord disease", "spinal cord disorder", "Spinal Cord Diseases", "Spinal Cord Disorder", "spinal cord; disease", "spinal cord diseases", "Spinal cord disorder", "Spinal Cord Disorders", "Spinal cord pathology", "Spinal cord--Diseases", "spinal cord disorders", "Neurologic myelopathy", "myelopathy (diagnosis)", "disease of spinal cord", "Myelopathy neurological", "disorder of spinal cord", "Spinal cord disorder NOS", "disease of the spinal cord", "Neurologic myelopathy, NOS", "Disease of spinal cord, NOS", "Abnormality of the spinal cord", "Abnormal spinal cord morphology", "Spinal cord disorder (disorder)", "Spinal cord disease or syndrome", "spinal cord disease or disorder", "spinal cord disorders (diagnosis)", "disease (or disorder); spinal cord", "Unspecified disease of spinal cord", "Spinal Cord Diseases and Syndromes", "disease or disorder of spinal cord", "Disease of spinal cord, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal cord disorder", "shortest_name_length": 10}
{"curie": "MONDO:0032606", "names": ["MC1DN2", "nuclear type mitochondrial complex I deficiency 2", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 2", "mitochondrial complex 1 deficiency, nuclear type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 2", "shortest_name_length": 6}
{"curie": "MONDO:0007057", "names": ["SFPKS", "HJCYS", "Cheney syndrome", "cheney syndrome", "Cheney Syndrome", "CHENEY SYNDROME", "Hajdu-Cheney Syndrome", "hajdu-cheney syndrome", "Hajdu-Cheney syndrome", "Hajdu Cheney Syndrome", "HAJDU-CHENEY SYNDROME", "cheney hajdu syndrome", "hajdu cheney syndrome", "Multicentric Osteolyses", "acrodentoosteodysplasia", "Multicentric Osteolysis", "Osteolysis, Multicentric", "Hereditary acrosteolysis", "Osteolyses, Multicentric", "arthrodentoosteodysplasia", "Arthrodentoosteodysplasia", "ARTHRODENTOOSTEODYSPLASIA", "Hereditary acroosteolysis", "arthrodento-osteodysplasia", "Serpentine fibula syndrome", "Arthrodentoosteodysplasias", "Hajdu-Cheney syndrome (HCS)", "acroosteolysis dominant type", "Arthro-dento-osteo dysplasia", "Acroosteolysis dominant type", "Familial acroosteolysis syndrome", "Hajdu-Cheney syndrome (disorder)", "arthrodento-osteodysplasia (ADOD)", "Familial acro-osteolysis syndrome", "hajdu-cheney syndrome (diagnosis)", "osteopathia dysplastica familiaris", "Hereditary acroosteolysis (disorder)", "Arthro-dento-osteo dysplasia syndrome", "SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME", "serpentine fibula-polycystic kidney syndrome", "serpentine fibula polycystic kidney syndrome", "Serpentine fibula polycystic kidney syndrome", "Serpentine Fibula-Polycystic Kidney Syndrome", "cranioskeletal dysplasia with acro-osteolysis", "serpentine fibula-polycystic kidneys syndrome", "hereditary osteodysplasia with acro-osteolysis", "acro-osteolysis-osteoporosis-changes in skull and mandible", "Acroosteolysis with osteoporosis and changes in skull and mandible", "acroosteolysis with osteoporosis and changes in skull and mandible", "Acroosteolysis with Osteoporosis and Changes in Skull and Mandible", "ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acroosteolysis dominant type", "shortest_name_length": 5}
{"curie": "MONDO:0005017", "names": ["Diffuse", "carcinoma, diffuse type", "Diffuse Gastric Adenocarcinoma", "diffuse stomach adenocarcinoma", "gastric diffuse adenocarcinoma", "diffuse gastric adenocarcinoma", "Gastric Diffuse Adenocarcinoma", "Diffuse Stomach Adenocarcinoma", "diffuse adenocarcinoma of stomach", "Diffuse Adenocarcinoma of Stomach", "diffuse type stomach adenocarcinoma", "stomach diffuse type adenocarcinoma", "Diffuse Adenocarcinoma of the Stomach", "diffuse adenocarcinoma of the stomach", "gastric cancer, diffuse adenocarcinoma", "stomach, diffuse adenocarcinoma of the", "stomach cancer, diffuse adenocarcinoma", "Adenocarcinoma of Linitis Plastica Type", "adenocarcinoma of linitis plastica type", "Adenocarcinoma of the Linitis Plastica Type", "adenocarcinoma of the linitis plastica type", "carcinoma, diffuse type (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diffuse gastric adenocarcinoma", "shortest_name_length": 7}
{"curie": "MONDO:0014467", "names": ["CMTRID", "RI-CMT type D", "COX6A1 Charcot-Marie-Tooth disease", "Charcot-Marie-Tooth disease recessive intermediate D", "Charcot-Marie-Tooth disease, recessive intermediate D", "CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE D", "Charcot-Marie-Tooth disease caused by mutation in COX6A1", "Charcot-Marie-Tooth disease recessive intermediate type D", "Charcot-Marie-Tooth disease, recessive Intermediate type D", "autosomal recessive intermediate Charcot-Marie-Tooth disease type D", "Autosomal recessive intermediate Charcot-Marie-Tooth disease type D", "Autosomal recessive intermediate Charcot-Marie-Tooth disease type D (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease recessive intermediate D", "shortest_name_length": 6}
{"curie": "MONDO:0009251", "names": ["FBP1D", "FBPase deficiency", "baker-Winegrad disease", "Fructosediphosphatase Deficiency", "Fructose-Biphosphatase Deficiency", "Fructose Biphosphatase Deficiency", "Deficiency, Fructosediphosphatase", "Fructose-biphosphatase deficiency", "Deficiency, Fructose-Biphosphatase", "Fructosediphosphatase Deficiencies", "Fructose-Biphosphatase Deficiencies", "Deficiencies, Fructosediphosphatase", "Deficiencies, Fructose-Biphosphatase", "Fructose 1,6 Diphosphatase Deficiency", "fructose 1,6-diphosphatase deficiency", "Fructose-1,6-diphosphatase deficiency", "fructose 1,6 diphosphatase deficiency", "Fructose-1,6-Diphosphatase Deficiency", "fructose-1,6-diphosphatase deficiency", "Deficiency, Fructose-1,6-Diphosphatase", "fructose-1,6-bisphosphatase deficiency", "Fructose-1,6-Bisphosphatase Deficiency", "Fructose 1,6 Bisphosphatase Deficiency", "Fructose-1, 6-diphosphatase deficiency", "FRUCTOSE-1,6-BISPHOSPHATASE DEFICIENCY", "Fructose-1,6-bisphosphatase deficiency", "Deficiency, Fructose-1,6-Bisphosphatase", "Fructose-1,6-Diphosphatase Deficiencies", "Deficiencies, Fructose-1,6-Diphosphatase", "Fructose-1,6-Bisphosphatase Deficiencies", "fructose 1 phosphate aldolase deficiency", "Deficiencies, Fructose-1,6-Bisphosphatase", "Fructose-biphosphatase deficiency (disorder)", "Hereditary fructose-1,6-phosphatase deficiency", "fructose 1,6-diphosphatase deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fructose-1,6-bisphosphatase deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C3272806", "names": ["Rectal Adenomatous Polyp", "Adenomatous Polyp of Rectum", "Adenomatous polyp of rectum", "Adenomatous Polyp of the Rectum", "Adenomatous polyp of rectum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenomatous polyp of rectum", "shortest_name_length": 24}
{"curie": "MONDO:0013987", "names": ["COXPD15", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15", "combined oxidative phosphorylation deficiency 15", "Combined oxidative phosphorylation defect type 15", "combined oxidative phosphorylation defect type 15", "MTFMT combined oxidative phosphorylation deficiency", "combined oxidative phosphorylation deficiency type 15", "COXPD15 - combined oxidative phosphorylation defect type 15", "Combined oxidative phosphorylation defect type 15 (disorder)", "combined oxidative phosphorylation defect type 15 (diagnosis)", "combined oxidative phosphorylation deficiency caused by mutation in MTFMT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation defect type 15", "shortest_name_length": 7}
{"curie": "MONDO:0000960", "names": ["diabetic angiopathy", "Diabetic angiopathy", "Diabetic Angiopathy", "Angiopathy, Diabetic", "Diabetic Angiopathies", "diabetic angiopathies", "Diabetic angiopathies", "Angiopathies, Diabetic", "Diabetic Vascular Disease", "Vascular Disease, Diabetic", "Diabetic Vascular Diseases", "Diabetic Vascular Disorder", "diabetic vascular disorder", "Diabetic vascular disorder", "Vascular Diseases, Diabetic", "Diabetic Vascular Complication", "diabetic peripheral angiopathy", "Diabetic peripheral angiopathy", "Diabetic vascular disorder NOS", "Diabetic Vascular Complications", "Vascular Complication, Diabetic", "Vascular Complications, Diabetic", "Diabetic peripheral vascular disease", "angiopathy; diabetes (manifestation)", "diabetes; angiopathy (manifestation)", "Diabetic peripheral vascular disorder", "Diabetes with peripheral circulatory disorder", "diabetes with peripheral circulatory disorder", "Diabetes with peripheral circulatory disorders", "Peripheral angiopathy due to diabetes mellitus", "diabetes mellitus with peripheral circulatory disorder", "Peripheral angiopathy due to diabetes mellitus (disorder)", "diabetes mellitus with peripheral circulatory disorder (diagnosis)", "Unspecified diabetes mellitus with peripheral circulatory complications"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diabetic peripheral angiopathy", "shortest_name_length": 19}
{"curie": "MONDO:0006792", "names": ["Hyperglobulinemic purpura", "hyperglobulinemic purpura", "Hyperglobulinemic Purpura", "Hyperglobulinemic Purpuras", "Purpura, Hyperglobulinemic", "Purpuras, Hyperglobulinemic", "Hyperglobulinemic purpura (disorder)", "Waldenstrom Hyperglobulinemic Purpura", "Waldenström Hyperglobulinemic Purpura", "Purpura, Waldenstrom Hyperglobulinemic", "Hyperglobulinemic Purpura, Waldenstrom", "Hyperglobulinemic Purpura of Waldenström", "Benign Hyperglobulinemic Purpura of Waldenström"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperglobulinemic purpura", "shortest_name_length": 25}
{"curie": "UMLS:C3897233", "names": ["Untreated Gemistocytic Astrocytoma", "untreated childhood gemistocytic astrocytoma", "Untreated Childhood Gemistocytic Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Untreated Childhood Gemistocytic Astrocytoma", "shortest_name_length": 34}
{"curie": "UMLS:C2930745", "names": ["Partial monosomy", "Partial Monosomy", "Monosomy, Partial", "Partial Monosomies", "Monosomies, Partial", "Partial monosomy (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Partial Monosomy", "shortest_name_length": 16}
{"curie": "MONDO:0100470", "names": ["asthma", "ASTHMA", "Asthma", "Asthmas", "Asthmatic", "br asthma", "asthmatic", "asthmatics", "Asthma NOS", "Asthma, NOS", "ASTHMA BRONCHIAL", "bronchial asthma", "asthma disorders", "Bronchial Asthma", "BRONCHIAL ASTHMA", "Asthma bronchial", "Bronchial asthma", "bronchitic asthma", "Asthma, Bronchial", "Bronchitic asthma", "Asthma (disorder)", "ASTHMA, BRONCHIAL", "asthma (diagnosis)", "Unspecified asthma", "Asthma, unspecified", "Bronchial asthma, NOS", "Airway hyperreactivity", "airway reactive disease", "reactive airway disease", "AIRWAY DISEASE REACTIVE", "Reactive airway disease", "bronchial hyperactivity", "Bronchial hyperactivity", "Reactive Airway Disease", "airway disease reactive", "Reactive airways disease", "airway diseases reactive", "reactive airways disease", "Bronchial Hyperreactivity", "Bronchial hyperreactivity", "bronchial hyperreactivity", "bronchial hypersensitivity", "hyperactive airway disease", "Hyperactive Airway Disease", "Hyperreactivity, Bronchial", "Bronchial hypersensitivity", "disease hyperactive airway", "Bronchial Hyperreactivities", "Disease;hyperactive airways", "hyperactive airways disease", "Reactive Airway Disease (AQ)", "Hyperreactive airway disease", "reactive airway disease (AQ)", "Hyperreactivities, Bronchial", "bronchial hyperresponsiveness", "Bronchial hyperresponsiveness", "BHR - Bronchial hyperreactivity", "Reactive airway disease (disorder)", "reactive airway disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "reactive airway disease", "shortest_name_length": 6}
{"curie": "UMLS:C0343890", "names": ["systemic cryptococcosis", "Systemic cryptococcosis", "Generalized cryptococcosis", "cryptococcosis; generalized", "generalized; cryptococcosis", "CRYPTOCOCCOSIS DISSEMINATED", "Disseminated cryptococcosis", "cryptococcosis; disseminated", "disseminated; cryptococcosis", "Extrapulmonary cryptococcosis", "Cryptococcosis extrapulmonary", "Systemic cryptococcosis (disorder)", "systemic cryptococcosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Systemic cryptococcosis", "shortest_name_length": 23}
{"curie": "UMLS:C0242084", "names": ["cerebral aneurysm rupture", "aneurysm cerebral rupture", "CEREBRAL ANEURYSM RUPTURE", "ruptured cerebral aneurysm", "RUPTURED CEREBRAL ANEURYSM", "Ruptured cerebral aneurysm", "Ruptured cerebral aneurysm (disorder)", "ruptured cerebral aneurysm (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ruptured cerebral aneurysm", "shortest_name_length": 25}
{"curie": "MONDO:0011690", "names": ["CAEND2", "Camurati Engelmann disease, type 2", "Camurati-Engelmann disease, type 2", "CAMURATI-ENGELMANN DISEASE, TYPE 2", "Progressive diaphyseal dysplasia with striations of the bones", "progressive diaphyseal dysplasia with striations of the bones"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Camurati-Engelmann disease, type 2", "shortest_name_length": 6}
{"curie": "UMLS:C0001828", "names": ["Agricultural Worker Disease", "Worker Disease, Agricultural", "Agricultural Worker Diseases", "Agricultural Workers Disease", "Disease, Agricultural Worker", "Diseases, Agricultural Worker", "Worker Diseases, Agricultural", "Agricultural Worker's Disease", "Agricultural Workers' Disease", "Agricultural Workers Diseases", "Disease, Agricultural Worker's", "Workers' Disease, Agricultural", "Worker's Disease, Agricultural", "Agricultural Worker's Diseases", "Agricultural Workers' Diseases", "Disease, Agricultural Workers'", "Worker's Diseases, Agricultural", "Diseases, Agricultural Worker's", "Workers' Diseases, Agricultural", "Diseases, Agricultural Workers'"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Agricultural Workers' Diseases", "shortest_name_length": 27}
{"curie": "UMLS:C1266115", "names": ["Mucosal Lentiginous Melanoma", "mucosal lentiginous melanoma", "Mucosal lentiginous melanoma", "Mucosal-lentiginous melanoma", "Mucosal Lentiginous Malignant Melanoma", "mucosal lentiginous melanoma (diagnosis)", "Mucosal lentiginous melanoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mucosal lentiginous melanoma", "shortest_name_length": 28}
{"curie": "MONDO:0800133", "names": ["Small lung", "Small lungs", "hypoplasia lung", "lung hypoplasia", "LUNG HYPOPLASIA", "Lung hypoplasia", "Hypoplastic lung", "hypoplasia lungs", "hypoplasia; lung", "LUNG, HYPOPLASIA", "Rudimentary lung", "lung; hypoplasia", "Hypoplastic lungs", "Hypoplasia of lung", "Underdeveloped lung", "Pulmonary Hypoplasia", "pulmonary hypoplasia", "Pulmonary hypoplasia", "hypoplasia; pulmonary", "Congenital small lung", "pulmonary; hypoplasia", "Poorly developed lungs", "Hypoplasia of lobe of lung", "Congenital hypoplasia of lung", "hypoplasia; respiratory system", "respiratory system; hypoplasia", "Congenital pulmonary hypoplasia", "pulmonary hypoplasia (diagnosis)", "Congenital hypoplasia of lung (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary hypoplasia", "shortest_name_length": 10}
{"curie": "UMLS:C3272530", "names": ["Intestinal NEC", "Intestinal NEC G3", "Intestinal Neuroendocrine Carcinoma", "Intestinal High Grade Neuroendocrine Carcinoma", "Intestinal Poorly Differentiated Endocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal Neuroendocrine Carcinoma", "shortest_name_length": 14}
{"curie": "MONDO:0015014", "names": ["COMMAD", "COMMAD syndrome", "coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness", "COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS", "Coloboma-osteopetrosis-microphthalmia-macrocephaly-albinism-deafness syndrome", "coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness; COMMAD"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness", "shortest_name_length": 6}
{"curie": "MONDO:0004789", "names": ["CHOLANGITIS", "cholangitis", "Cholangitis", "cholangeitis", "Cholangitides", "Cholangitis NOS", "Cholangitis, NOS", "bile duct inflammation", "Bile duct inflammation", "INFLAMMATION BILE DUCT", "Inflammation bile duct", "Cholangitis (disorder)", "cholangitis (diagnosis)", "inflammation; bile duct", "bile duct; inflammation", "Biliary Tract Infection", "Biliary tract infection", "biliary tract infection", "biliary tree inflammation", "inflammation of biliary tree"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholangitis", "shortest_name_length": 11}
{"curie": "UMLS:C0400969", "names": ["Liver transplant failure", "liver transplant failure", "transplant; failure, liver", "failure; transplant, liver", "Liver transplant failure (disorder)", "liver transplant failure (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liver transplant failure", "shortest_name_length": 24}
{"curie": "UMLS:C5418565", "names": ["Locally Advanced Pancreatobiliary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Pancreatobiliary Carcinoma", "shortest_name_length": 43}
{"curie": "UMLS:C1335658", "names": ["Radiation-Induced Intracranial Meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radiation-Induced Intracranial Meningioma", "shortest_name_length": 41}
{"curie": "MONDO:0022425", "names": ["Abuelo Forman Rubin syndrome", "alpha-thalassemia-abnormal morphogenesis", "homozygous alpha-thalassemia, genital abnormalities, and terminal transverse limb defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alpha-thalassemia-abnormal morphogenesis", "shortest_name_length": 28}
{"curie": "UMLS:C4553869", "names": ["I", "Stage I Bladder Cancer", "Stage I Bladder Cancer AJCC v8", "Stage I Bladder Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Bladder Cancer AJCC v8", "shortest_name_length": 1}
{"curie": "MONDO:0024864", "names": ["Medium/Large Size Posterior Uveal Melanoma", "medium/large size posterior uveal melanoma", "posterior uvea melanoma, medium/large size", "uveal melanoma, posterior, medium/large size", "melanoma, posterior uveal, medium/large size", "medium/large size ciliary body and choroid melanoma", "Medium/Large Size Ciliary Body and Choroid Melanoma", "ciliary body and choroid melanoma, medium/large size", "intraocular melanoma ciliary body and choroid, medium/large size", "melanoma, intraocular ciliary body and choroid, medium/large size"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "medium/large size posterior uveal melanoma", "shortest_name_length": 42}
{"curie": "UMLS:C0160392", "names": ["Closed injury of liver", "Injury of liver without open wound into abdominal cavity", "Injury to liver without mention of open wound into cavity", "Injury to Liver without mention of Open Wound into Cavity", "Injury of liver without open wound into abdominal cavity (disorder)", "Unspecified injury of liver without open wound into abdominal cavity", "Unspecified injury to liver without mention of open wound into cavity", "Injury to liver without mention of open wound into cavity, unspecified injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of liver without open wound into abdominal cavity", "shortest_name_length": 22}
{"curie": "MONDO:0000591", "names": ["primary cardiomyopathy", "intrinsic cardiomyopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intrinsic cardiomyopathy", "shortest_name_length": 22}
{"curie": "UMLS:C3544094", "names": ["Arterial thromboembolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arterial thromboembolism", "shortest_name_length": 24}
{"curie": "UMLS:C5555105", "names": ["Nasopharyngeal Melanoma", "Nasopharyngeal Mucosal Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasopharyngeal Melanoma", "shortest_name_length": 23}
{"curie": "MONDO:0022178", "names": ["chromosome 13q-mosaicism", "Chromosome 13q-mosaicism", "Mosiacism of chromosome 13q"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 13q-mosaicism", "shortest_name_length": 24}
{"curie": "MONDO:0014907", "names": ["SRTD15", "SHORT-RIB THORACIC DYSPLASIA 15 WITH POLYDACTYLY", "short-rib thoracic dysplasia 15 with polydactyly", "short-rib thoracic dysplasia 15 with polydactyly; SRTD15"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short-rib thoracic dysplasia 15 with polydactyly", "shortest_name_length": 6}
{"curie": "MONDO:0002984", "names": ["Reticulohistiocytoma", "reticulohistiocytoma", "solitary histiocytoma", "Reticulohistiocytomas", "Giant cell histiocytoma", "Reticulohistiocytoma cutis", "Reticulohistiocytic granuloma", "reticulohistiocytic granuloma", "Solitary Reticulohistiocytoma", "solitary reticulohistiocytoma", "solitary Reticulohistiocytoma", "Reticulohistiocytic Granuloma", "Solitary reticulohistiocytoma", "granuloma; reticulohistiocytic", "GRANULOMA, RETICULOHISTIOCYTIC", "solitary reticulohistiocytosis", "reticulohistiocytic; granuloma", "Solitary reticulohistiocytoma (disorder)", "Reticulohistiocytic granuloma (morphologic abnormality)", "reticulohistiocytic granuloma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "reticulohistiocytic granuloma", "shortest_name_length": 20}
{"curie": "MONDO:0011163", "names": ["MHS5", "Mhs5", "malignant hyperthermia susceptibility 5", "susceptibility to malignant hyperthermia 5", "malignant hyperpyrexia susceptibility type 5", "Malignant hyperthermia susceptibility type 5", "CACNA1S malignant hyperthermia of anesthesia", "Malignant hyperpyrexia susceptibility type 5", "MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 5", "malignant hyperthermia, susceptibility to, 5", "malignant hyperthermia susceptibility type 5", "malignant hyperthermia, susceptibility to, type 5", "malignant hyperthermia of anesthesia caused by mutation in CACNA1S"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant hyperthermia, susceptibility to, 5", "shortest_name_length": 4}
{"curie": "MONDO:0013507", "names": ["CGD3", "CDG3", "autosomal recessive chronic granulomatous disease 3", "chronic granulomatous disease 3, autosomal recessive", "chronic granulomatous disease due to NCF4 deficiency", "GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, 3", "CGD, autosomal recessive cytochrome B-positive, type 3", "granulomatous disease, chronic, due to Ncf4 deficiency", "autosomal recessive cytochrome b-positive CGD type III", "GRANULOMATOUS DISEASE, CHRONIC, DUE TO NCF4 DEFICIENCY", "CGD, AUTOSOMAL RECESSIVE CYTOCHROME b-POSITIVE, TYPE III", "autosomal recessive chronic granulomatous disease cytochrome b-positive type III", "granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 3", "granulomatous disease, chronic, autosomal recessive, cytochrome b-POSITIVE, type III", "GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 3", "shortest_name_length": 4}
{"curie": "UMLS:C0349757", "names": ["AV Graft Thrombosis", "Arteriovenous graft thrombosis", "Arteriovenous Graft Thrombosis", "Arteriovenous graft thrombosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arteriovenous graft thrombosis", "shortest_name_length": 19}
{"curie": "UMLS:C5557354", "names": ["Cervical Florid Reactive Lymphoid Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Florid Reactive Lymphoid Hyperplasia", "shortest_name_length": 45}
{"curie": "UMLS:C0269936", "names": ["Childbed fever", "childbed fever", "Puerperal fever", "fever puerperal", "puerperal fever", "puerperal; fever", "puerperal sepsis", "fever postpartum", "Puerperal sepsis", "postpartum fever", "Postpartum Fever", "PUERPERAL SEPSIS", "sepsis puerperal", "fever; puerperal", "Postpartum fever", "Sepsis;puerperal", "Fever, puerperal", "puerperal pyrexia", "Postpartum sepsis", "Puerperal pyrexia", "sepsis; puerperal", "Postpartum Sepsis", "Postpartum Sepses", "Sepsis postpartum", "Pyrexia puerperal", "postpartum sepsis", "SEPSIS POSTPARTUM", "pyrexia; puerperal", "Sepsis, Postpartum", "Postpartum Pyrexia", "puerperium; sepsis", "Postpartum pyrexia", "Sepses, Postpartum", "puerperium; pyrexia", "Puerperal fever NOS", "Postpartum fever NOS", "Puerperal septicemia", "puerperal septicaemia", "Puerperal septicaemia", "Puerperal pyrexia NOS", "puerperium; septicemia", "Puerperal pyrexia, NOS", "fever; following delivery", "Postpartum fever (finding)", "Puerperal sepsis (disorder)", "puerperal sepsis (diagnosis)", "Puerperal pyrexia (disorder)", "puerperal pyrexia (diagnosis)", "puerperalis; febris puerperalis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Puerperal sepsis", "shortest_name_length": 14}
{"curie": "UMLS:C2981624", "names": ["Stage I Intrahepatic Cholangiocarcinoma AJCC v7", "Stage I Intrahepatic Bile Duct Cancer (Cholangiocarcinoma)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Intrahepatic Cholangiocarcinoma AJCC v7", "shortest_name_length": 47}
{"curie": "MONDO:0008586", "names": ["TEF", "Ea-Tef", "te fistula", "Esophagotracheal fistula", "esophagotracheal fistula", "Esophagotracheal Fistula", "fistula tracheoesophageal", "tracheoesophageal fistula", "TRACHEOESOPHAGEAL FISTULA", "Fistula, Esophagotracheal", "Tracheoesophageal fistula", "Tracheoesophageal Fistula", "esophagotracheal; fistula", "fistula; esophagotracheal", "Esophagotracheal Fistulas", "Oesophagotracheal fistula", "TRACHEO-ESOPHAGEAL FISTULA", "Fistulas, Esophagotracheal", "Fistula, Tracheoesophageal", "Tracheo-esophageal fistula", "tracheo-esophageal fistula", "fistula; tracheoesophageal", "fistula tracheo-esophageal", "Tracheo-esophageal Fistula", "Tracheoesophageal Fistulas", "TRACHED-ESOPHAGEAL FISTULA", "tracheoesophageal; fistula", "tracheoesophageal fistulas", "fistulas tracheoesophageal", "tracheo-oesophageal fistula", "Fistulas, Tracheoesophageal", "TRACHEO-OESOPHAGEAL FISTULA", "Tracheo-oesophageal fistula", "FISTULA, TRACHEO-ESOPHAGEAL", "Tracheo-esophageal fistula NOS", "Tracheoesophageal fistula, NOS", "Tracheo-oesophageal fistula NOS", "TOF - Tracheoesophageal fistula", "H-type tracheoesophageal fistula", "TOF - Tracheo-esophageal fistula", "TOF - Tracheo-oesophageal fistula", "Isolated tracheoesophageal fistula", "Tracheoesophageal fistula (disorder)", "tracheoesophageal fistula (diagnosis)", "Esophageal Atresia Tracheoesophageal Fistula", "esophageal atresia/tracheoesophageal fistula", "Esophageal Atresia-Tracheoesophageal Fistula", "Abnormal connection between trachea and esophagus", "Abnormal connection between trachea and oesophagus", "esophageal atresia and/or tracheoesophageal fistula", "tracheoesophageal fistula with or without esohageal atresia", "Tracheoesophageal fistula with or without esophageal atresia", "Esophageal atresia with or without tracheoesophageal fistula", "ESOPHAGEAL ATRESIA WITH OR WITHOUT TRACHEOESOPHAGEAL FISTULA", "esophageal atresia with or without tracheoesophageal fistula", "tracheoesophageal fistula with or without esophageal atresia", "TRACHEOESOPHAGEAL FISTULA WITH OR WITHOUT ESOPHAGEAL ATRESIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophageal atresia/tracheoesophageal fistula", "shortest_name_length": 3}
{"curie": "UMLS:C0334435", "names": ["Precancerous Melanosis", "Precancerous melanosis", "Precancerous melanosis NOS", "Precancerous melanosis, NOS", "precancerous melanosis of skin", "Precancerous melanosis (disorder)", "precancerous melanosis of skin (diagnosis)", "Precancerous melanosis (morphologic abnormality)", "Melanosis circumscripta precancerosa of Dubreuilh"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Precancerous melanosis", "shortest_name_length": 22}
{"curie": "MONDO:0023175", "names": ["Fontaine farriaux blanckaert syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fontaine farriaux blanckaert syndrome", "shortest_name_length": 37}
{"curie": "MONDO:0006141", "names": ["Cervical Villoglandular Carcinoma", "cervical villoglandular carcinoma", "Cervical Villoglandular Adenocarcinoma", "cervical villoglandular adenocarcinoma", "villoglandular adenocarcinoma of the cervix", "cervical adenocarcinoma, villoglandular variant", "Cervical Adenocarcinoma, Villoglandular Variant", "villoglandular variant cervical mucinous adenocarcinoma", "Cervical Mucinous Adenocarcinoma, Villoglandular Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical villoglandular adenocarcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C4744972", "names": ["Steroid-Refractory Pneumonitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Steroid-Refractory Pneumonitis", "shortest_name_length": 30}
{"curie": "MONDO:0009488", "names": ["KPC", "Kpc with associated malformations", "KPC WITH ASSOCIATED MALFORMATIONS", "KPC with Associated Malformations", "KERATOCONUS POSTICUS CIRCUMSCRIPTUS", "keratoconus posticus circumscriptus", "Keratoconus posticus circumscriptus", "keratoconus posticus CIRCUMSCRIPTUS", "Keratoconus Posticus Circumscriptus with Associated Malformations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratoconus posticus circumscriptus", "shortest_name_length": 3}
{"curie": "OMIM:611739", "names": ["BMND8", "OSTEOPOROSIS, SUSCEPTIBILITY TO", "BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 5}
{"curie": "UMLS:C4524370", "names": ["Sinonasal Cancer by AJCC v8 Stage", "Sinonasal Carcinoma by AJCC v8 Stage", "Nasal Cavity and Paranasal Sinus Cancer by AJCC v8 Stage", "Nasal Cavity and Paranasal Sinus Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Cancer by AJCC v8 Stage", "shortest_name_length": 33}
{"curie": "UMLS:C0919866", "names": ["nevus eye", "eye nevus", "Eye nevus", "Eye naevus", "nevus; site eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eye nevus", "shortest_name_length": 9}
{"curie": "MONDO:0022654", "names": ["cardiomyopathy-hypogonadism-collagenoma syndrome", "Cardiomyopathy hypogonadism collagenoma syndrome", "Cardiomyopathy-Hypogonadism-Collagenoma Syndrome", "cardiomyopathy hypogonadism collagenoma syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiomyopathy hypogonadism collagenoma syndrome", "shortest_name_length": 48}
{"curie": "MONDO:0001040", "names": ["NASOPHARYNGITIS", "Nasopharyngitis", "nasopharyngitis", "Rhinopharyngitis", "rhinopharyngitis", "Nasopharyngitides", "Nasopharyngitis NOS", "Nasopharyngitis, NOS", "Rhinopharyngitis, NOS", "chronic nasopharyngitis", "Nasopharyngitis;chronic", "Chronic nasopharyngitis", "nasopharyngitis; chronic", "chronic; nasopharyngitis", "nasopharynx inflammation", "Nasopharyngitis (disorder)", "inflammation of nasopharynx", "Chronic nasopharyngitis (disorder)", "chronic nasopharyngitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasopharyngitis", "shortest_name_length": 15}
{"curie": "UMLS:C0272409", "names": ["Nontraumatic splenic rupture", "rupture; spleen, spontaneous", "spleen; rupture, spontaneous", "Spontaneous rupture of spleen", "rupture; spleen, nontraumatic", "Splenic rupture, nontraumatic", "spleen; rupture, nontraumatic", "Non-traumatic rupture of spleen", "Nontraumatic splenic rupture (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nontraumatic splenic rupture", "shortest_name_length": 28}
{"curie": "UMLS:C4524842", "names": ["Locally Advanced Paraganglioma", "Locally Advanced Malignant Paraganglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Paraganglioma", "shortest_name_length": 30}
{"curie": "MONDO:0015845", "names": ["uterine cervical aplasia and agenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine cervical aplasia and agenesis", "shortest_name_length": 37}
{"curie": "MONDO:0005852", "names": ["MS", "ms", "mitral stenoses", "Mitral stenosis", "Mitral Stenoses", "Mitral Stenosis", "mitral stenosis", "MITRAL STENOSIS", "stenosis; mitral", "stenoses, mitral", "Stenosis, Mitral", "stenosis, mitral", "mitral; stenosis", "Stenoses, Mitral", "stricture; mitral", "mitral; stricture", "MS - Mitral stenosis", "mitral valve stenosis", "Mitral Valve Stenoses", "Mitral valve stenosis", "mitral valve stenoses", "MITRAL VALVE STENOSIS", "Mitral Valve Stenosis", "Stenoses, Mitral Valve", "stenosis, mitral valve", "Stenosis, Mitral Valve", "Valve Stenosis, Mitral", "MITRAL VALVE, STENOSIS", "valve stenosis, mitral", "stenoses, mitral valve", "valve stenoses, mitral", "Valve Stenoses, Mitral", "Mitral valve stenosis, NOS", "mitral stenosis (diagnosis)", "Mitral valve stenosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitral valve stenosis", "shortest_name_length": 2}
{"curie": "MONDO:0005635", "names": ["adenomyoma", "Adenomyoma", "Adenomyomas", "ADENOMYOMA, BENIGN", "adenomyoma, benign", "adenomyoma (morphologic abnormality)", "Adenomyoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenomyoma", "shortest_name_length": 10}
{"curie": "MONDO:0010038", "names": ["IGF1R", "IGF1RES", "IGF-I Resistance", "IGF-I resistance", "IGF-I RESISTANCE", "IGF-1 resistance", "resistance to IGF-1", "Resistance to IGF-1", "Somatomedin C resistance", "Somatomedin-C Resistance", "Somatomedin-c resistance to", "Somatomedin-C, resistance to", "SOMATOMEDIN-C, RESISTANCE TO", "Somatomedin C, Resistance To", "Insulin Growth Factor I Resistance", "Somatomedin end-organ insensitivity to", "Somatomedin, end-organ insensitivity to", "SOMATOMEDIN, END-ORGAN INSENSITIVITY TO", "Somatomedin, End-Organ Insensitivity To", "insulin-like growth factor 1 resistance to", "INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO", "insulin-like growth factor I, resistance to", "Insulin-Like Growth Factor I, Resistance To", "Insulin-like growth factor-1 (IGF-1) resistance", "IGF-1 (insulin-like growth factor 1) resistance", "insulin-like growth factor-1 (IGF-1) resistance", "insulin-like growth factor-1 (IGF-1) resistance (diagnosis)", "growth delay due to insulin-like growth factor I resistance", "Growth delay due to insulin-like growth factor I resistance", "Growth delay due to insulin-like growth factor 1 resistance", "Growth delay due to insulin-like growth factor I resistance (disorder)", "insulin-like Growth Factor I, resistance to, due to increased binding Protein", "INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO, DUE TO INCREASED BINDING PROTEIN", "Insulin-Like Growth Factor I, Resistance to, due to Increased Binding Protein"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "growth delay due to insulin-like growth factor I resistance", "shortest_name_length": 5}
{"curie": "MONDO:0019143", "names": ["Angiostrongylosis", "ANGIOSTRONGYLIASIS", "Angiostrongyliasis", "angiostrongyliasis", "Angiostrongylus Infection", "Angiostrongylus infection", "Infection, Angiostrongylus", "Angiostrongylus Infections", "Infection by Angiostrongylus", "angiostrongyliasis (diagnosis)", "Infection by Angiostrongylus, NOS", "Infection caused by Angiostrongylus", "Infection caused by Angiostrongylus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angiostrongyliasis", "shortest_name_length": 17}
{"curie": "MONDO:0013734", "names": ["MCOPS11", "syndromic microphthalmia 11", "microphthalmia, syndromic 11", "MICROPHTHALMIA, SYNDROMIC 11", "VAX1 syndromic microphthalmia", "microphthalmia, syndromic type 11", "syndromic microphthalmia caused by mutation in VAX1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microphthalmia, syndromic 11", "shortest_name_length": 7}
{"curie": "UMLS:C1336102", "names": ["Ureter Cancer Stage 0a", "Stage 0a Ureter Cancer", "Stage 0a Ureter Carcinoma", "Stage 0a Ureteral Carcinoma", "Stage 0a Carcinoma of Ureter", "Stage 0a Ureter Cancer AJCC v7", "Stage 0a Carcinoma of the Ureter", "Stage 0a Ureter Urothelial Carcinoma", "Ureter Papillary Noninvasive Carcinoma", "Stage 0a Ureter Urothelial Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0a Ureter Cancer AJCC v7", "shortest_name_length": 22}
{"curie": "MONDO:0007841", "names": ["SPS", "ICPPS", "Scott Taor syndrome", "Scott-Taor syndrome", "SCOTT-TAOR SYNDROME", "Small patella syndrome", "SMALL PATELLA SYNDROME", "small patella syndrome", "ischiopatellar dysplasia", "Ischiopatellar dysplasia", "ISCHIOPATELLAR DYSPLASIA", "coxopodopatellar syndrome", "coxopodipatellar syndrome", "Coxopodopatellar Syndrome", "COXOPODOPATELLAR SYNDROME", "Coxopodopatellar syndrome", "Coxo-podo-patellar syndrome", "coxo-podo-patellar syndrome", "ISCHIOCOXOPODOPATELLAR SYNDROME", "ischiocoxopodopatellar syndrome", "Coxopodopatellar syndrome (disorder)", "Patella aplasia, coxa vara, tarsal synostosis", "patella aplasia, coxa vara, tarsal synostosis", "Patella Aplasia, Coxa Vara, And Tarsal Synostosis", "patella aplasia, coxa vara, and tarsal synostosis", "PATELLA APLASIA, COXA VARA, AND TARSAL SYNOSTOSIS", "Congenital coxa vara, patella aplasia and tarsal synostosis", "congenital coxa vara, patella aplasia and tarsal synostosis", "ischiocoxopodopatellar syndrome with or without pulmonary arterial hypertension", "ISCHIOCOXOPODOPATELLAR SYNDROME WITH OR WITHOUT PULMONARY ARTERIAL HYPERTENSION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coxopodopatellar syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0018725", "names": ["dup(7)(q36.3)", "7q36.3 microduplication syndrome", "corpus callosum agenesis-macrocephaly-hypertelorism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corpus callosum agenesis-macrocephaly-hypertelorism syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0013393", "names": ["distal del(7)(q11.23)", "distal monosomy 7q11.23", "distal 7q11.23 microdeletion syndrome", "distal chromosome 7Q11.23 deletion syndrome", "DISTAL CHROMOSOME 7q11.23 DELETION SYNDROME", "chromosome 7q11.23 deletion syndrome, distal, 1.2mb", "chromosome 7q11.23 deletion syndrome, distal, 1.2-MB", "CHROMOSOME 7q11.23 DELETION SYNDROME, DISTAL, 1.2-MB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal 7q11.23 microdeletion syndrome", "shortest_name_length": 21}
{"curie": "UMLS:C0877089", "names": ["Vaginal mucosal blistering"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal mucosal blistering", "shortest_name_length": 26}
{"curie": "UMLS:C5556431", "names": ["POLE-Ultramutated Endometrial Endometrioid Carcinoma", "POLE-Ultra-Mutated Endometrial Endometrioid Carcinoma", "POLE-Ultramutated Endometrial Endometrioid Adenocarcinoma", "POLE-Ultra-Mutated Endometrial Endometrioid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "POLE-Ultramutated Endometrial Endometrioid Adenocarcinoma", "shortest_name_length": 52}
{"curie": "MONDO:0011504", "names": ["MHAC", "MICROHYDRANENCEPHALY", "microhydranencephaly", "Microhydranencephaly", "MHAC - microhydranencephaly", "hydranencephaly and microcephaly", "Hydranencephaly and microcephaly", "HYDRANENCEPHALY AND MICROCEPHALY", "NDE1-related microhydranencephaly", "nudE neurodevelopment protein 1-related microhydranencephaly", "nudE neurodevelopment protein 1-related microhydranencephaly (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "NDE1-related microhydranencephaly", "shortest_name_length": 4}
{"curie": "UMLS:C4727416", "names": ["Recurrent Parotid Gland Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Parotid Gland Squamous Cell Carcinoma", "shortest_name_length": 47}
{"curie": "MONDO:0020001", "names": ["respiratory or thoracic malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "respiratory or thoracic malformation", "shortest_name_length": 36}
{"curie": "MONDO:0013650", "names": ["hypt10", "Hypt10", "HYPT10", "HYPOTRICHOSIS 10", "hypotrichosis 10", "hypotrichosis type 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotrichosis 10", "shortest_name_length": 6}
{"curie": "UMLS:C0853314", "names": ["Soft tissue inflammation", "soft tissue inflammation", "inflammation soft tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Soft tissue inflammation", "shortest_name_length": 24}
{"curie": "UMLS:C4726545", "names": ["Refractory Metastatic Digestive System Carcinoma", "Refractory Metastatic Gastrointestinal System Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Metastatic Digestive System Carcinoma", "shortest_name_length": 48}
{"curie": "MONDO:0100053", "names": ["anaphylaxis", "Anaphylaxis", "ANAPHYLAXIS", "allergy; shock", "Allergic shock", "shock; allergy", "allergic shock", "ANAPHYLACTIC SHOCK", "anaphylactic shock", "Anaphylactic Shock", "Anaphylactic shock", "Shock;anaphylactic", "shock; anaphylactic", "Anaphylactoid Shock", "anaphylactic; shock", "Shock, anaphylactic", "Shock, Anaphylactic", "Systemic anaphylaxis", "Shock, Anaphylactoid", "systemic anaphylaxis", "Anaphylactic syndrome", "ANAPHYLACTIC REACTION", "anaphylactic reaction", "Anaphylactic reaction", "Anaphylactic Reaction", "REACTION, ANAPHYLACTIC", "Reaction, Anaphylactic", "anaphylactic reactions", "Anaphylaxis (disorder)", "Anaphylactic Reactions", "Anaphylactoid Reaction", "Reaction, Anaphylactoid", "Generalized anaphylaxis", "anaphylaxis (diagnosis)", "Anaphylactoid Reactions", "Generalised anaphylaxis", "Anaphylaxis, generalized", "Shock due to anaphylaxis", "ANAPHYLAXIS, GENERALIZED", "Systemic anaphylactic reaction", "Anaphylactic shock, unspecified", "Shock due to anaphylaxis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anaphylaxis", "shortest_name_length": 11}
{"curie": "UMLS:C0021645", "names": ["Insulin Coma", "Insulin coma", "coma insulin", "Coma;insulin", "insulin coma", "Coma, Insulin", "insulin shock", "Insulin coma NOS", "Insulin coma (disorder)", "insulin coma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Insulin Coma", "shortest_name_length": 12}
{"curie": "UMLS:C0015395", "names": ["burn eye", "Eye Burn", "eye burn", "EYE BURNS", "Eye burns", "burn; eye", "burns eye", "Burn, Eye", "Eye Burns", "burn eyes", "eye burns", "burns eyes", "Burns, Eye", "burned eye", "Burns eyes", "Burn of eye", "burning eye", "eye burning", "burning eyes", "eyes burning", "burns of eye", "Eye burns NOS", "burns of eyes", "burning in eyes", "Burn of eye region", "burns of eye (diagnosis)", "Burn of eye region (disorder)", "burns of eyes (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eye Burns", "shortest_name_length": 8}
{"curie": "UMLS:C1336912", "names": ["Endometrial Endometrioid Adenocarcinoma with Small Nonvillous Papillae"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endometrial Endometrioid Adenocarcinoma with Small Nonvillous Papillae", "shortest_name_length": 70}
{"curie": "MONDO:0008533", "names": ["Polydontia", "Extra tooth", "Hyperdontia", "Extra teeth", "extra; teeth", "Supernumary teeth", "Supplemental tooth", "Supplemental teeth", "supernumerary tooth", "Supernumerary Teeth", "Supernumerary tooth", "supplementary teeth", "Supernumerary teeth", "Supernumerary Tooth", "Supplementary teeth", "Supplementary tooth", "supernumerary teeth", "Multiple hyperdontia", "Tooth, supernumerary", "Teeth, Supernumerary", "Tooth, Supernumerary", "teeth, supernumerary", "teeth; supernumerary", "TEETH, SUPERNUMERARY", "Supernumary dentition", "Increased tooth count", "Supplemental dentition", "More teeth than normal", "Supplemental teeth, NOS", "SN - Supernumerary tooth", "Supernumerary teeth, NOS", "Increased number of teeth", "Supplemental tooth (disorder)", "Supernumerary teeth (disorder)", "supernumerary teeth were noted", "Supernumerary tooth (disorder)", "supernumerary teeth (diagnosis)", "supernumerary tooth (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "teeth, supernumerary", "shortest_name_length": 10}
{"curie": "UMLS:C4288000", "names": ["Vulvar Small Cell Carcinoma", "Vulvar Small Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Small Cell Neuroendocrine Carcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C4509020", "names": ["Isolated bone marrow mastocytosis", "Isolated bone marrow mastocytosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Isolated bone marrow mastocytosis", "shortest_name_length": 33}
{"curie": "MONDO:0017387", "names": ["ES", "Epithelioid sarcoma", "Epithelioid Sarcoma", "epithelioid sarcoma", "epithelioid; sarcoma", "Sarcoma, Epithelioid", "Epithelioid sarcomas", "sarcoma; epithelioid", "Epithelioid Sarcomas", "Sarcomas, Epithelioid", "Epithelioid sarcoma NOS", "Epithelioid cell sarcoma", "epithelioid cell sarcoma", "Epithelioid Cell Sarcoma", "Epithelioid sarcoma (disorder)", "epithelioid sarcoma (diagnosis)", "Epithelioid sarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epithelioid sarcoma", "shortest_name_length": 2}
{"curie": "MONDO:0009171", "names": ["endothelial dystrophy, congenital hereditary, with nail hypoplasia", "Endothelial Dystrophy, Congenital Hereditary, with Nail Hypoplasia", "ENDOTHELIAL DYSTROPHY, CONGENITAL HEREDITARY, WITH NAIL HYPOPLASIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endothelial dystrophy, congenital hereditary, with nail hypoplasia", "shortest_name_length": 66}
{"curie": "MONDO:0007249", "names": ["CAMPTOBRACHYDACTYLY", "Camptobrachydactyly", "camptobrachydactyly", "Camptobrachydactyly (disorder)", "short foot/brachydactyly of toes, camptodactyly, brachydactyly", "Short foot-brachydactyly of toes, camptodactyly , brachydactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "camptobrachydactyly", "shortest_name_length": 19}
{"curie": "MONDO:0015797", "names": ["UVSS", "UV-sensitive syndrome", "UV-Sensitive Syndrome", "UV sensitive syndrome", "Ultraviolet sensitive syndrome", "UVSS - ultraviolet sensitive syndrome", "Ultraviolet sensitive syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "UV-sensitive syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0009917", "names": ["PHA1B", "PHA1B1", "generalized PHA1", "Generalized PHA1", "Autosomal recessive PHA1", "autosomal recessive PHA 1", "PHA I, AUTOSOMAL RECESSIVE", "PHA I, autosomal recessive", "pseudohypoaldosteronism type 1, recessive", "generalized pseudohypoaldosteronism type 1", "Generalized pseudohypoaldosteronism type 1", "Autosomal recessive pseudohypoaldosteronism type 1", "pseudohypoaldosteronism type 1 autosomal recessive", "autosomal recessive pseudohypoaldosteronism type 1", "Pseudohypoaldosteronism Type 1, Autosomal Recessive", "PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL RECESSIVE", "pseudohypoaldosteronism, type I, autosomal recessive", "Pseudohypoaldosteronism, Type I, Autosomal Recessive", "PSEUDOHYPOALDOSTERONISM, TYPE IB1, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive pseudohypoaldosteronism type 1", "shortest_name_length": 5}
{"curie": "UMLS:C5418900", "names": ["Platinum-Resistant Malignant Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Platinum-Resistant Malignant Germ Cell Tumor", "shortest_name_length": 44}
{"curie": "MONDO:0018128", "names": ["phalangeal osteolysis", "phalangeal microgeodic syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phalangeal microgeodic syndrome", "shortest_name_length": 21}
{"curie": "UMLS:C0346989", "names": ["Peritoneal seedling", "Peritoneal metastases", "Metastasis to peritoneum", "Metastases to peritoneum", "Metastasis to the Peritoneum", "Metastases to peritoneum, NOS", "Cancer metastatic to peritoneum", "Metastatic Neoplasm to the Peritoneum", "Secondary malignant peritoneal deposit", "peritoneal neoplasm malignant secondary", "Secondary malignant neoplasm of peritoneum", "Metastatic malignant neoplasm to peritoneum", "Metastatic malignant neoplasm of peritoneum", "metastasis of malignant neoplasm to peritoneum", "Metastatic Malignant Neoplasm to the Peritoneum", "Metastatic Malignant Neoplasm in the Peritoneum", "Secondary malignant neoplasm of the peritoneum, NOS", "Metastatic malignant neoplasm to the peritoneum, NOS", "Metastatic malignant neoplasm to peritoneum (disorder)", "Secondary malignant neoplasm of peritoneum (diagnosis)", "metastasis of malignant neoplasm to peritoneum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to peritoneum", "shortest_name_length": 19}
{"curie": "UMLS:C1710026", "names": ["SEF", "Sclerosing Epithelioid Fibrosarcoma", "Sclerosing epithelioid fibrosarcoma", "Sclerosing epithelioid fibrosarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sclerosing Epithelioid Fibrosarcoma", "shortest_name_length": 3}
{"curie": "UMLS:C4525665", "names": ["Digestive System Neuroendocrine Tumor by AJCC v7 Stage", "Digestive System Neuroendocrine Neoplasm by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Digestive System Neuroendocrine Tumor by AJCC v7 Stage", "shortest_name_length": 54}
{"curie": "UMLS:C0278841", "names": ["relapsed testis cancer", "testis cancer, relapsed", "Testis cancer recurrent", "recurrent testis cancer", "testis cancer, recurrent", "Relapsed Cancer of Testis", "testicle cancer, relapsed", "Relapsed Testicular Cancer", "Recurrent Cancer of Testis", "relapsed testicular cancer", "testicle cancer, recurrent", "testicle cancer, refractory", "testicular cancer, relapsed", "Recurrent Testicular Cancer", "recurrent testicular cancer", "testicular cancer, recurrent", "Relapsed Cancer of the Testis", "relapsed cancer of the testis", "cancer of the testis, relapsed", "recurrent cancer of the testis", "Recurrent Cancer of the Testis", "cancer of the testis, recurrent", "recurrent testicular germ cell tumor", "recurrent or refractory testicular cancer", "recurrent malignant testicular germ cell tumor", "Recurrent Malignant Testicular Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testis cancer recurrent", "shortest_name_length": 22}
{"curie": "UMLS:C0751294", "names": ["Spatial Memory Disorder", "Spatial Memory Disorders", "Memory Disorder, Spatial", "Memory Disorders, Spatial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Memory Disorder, Spatial", "shortest_name_length": 23}
{"curie": "MONDO:0018945", "names": ["MLS", "MCLDS", "mcleod syndrome", "MCLEOD SYNDROME", "McLeod syndrome", "McLeod Syndrome", "McLeod phenotype", "mcleods syndrome", "MCLEOD PHENOTYPE", "McCleod syndrome", "Kx null phenotype", "X-linked McLeod syndrome", "McLeod phenotype (finding)", "Blood group deletion syndrome", "McLeod type neuroacanthocytosis", "neuroacanthocytosis, McLeod type", "Neuroacanthocytosis, Mcleod Type", "NEUROACANTHOCYTOSIS, MCLEOD TYPE", "McLeod neuroacanthocytosis syndrome", "Blood group deletion syndrome (disorder)", "MCLEOD SYNDROME WITH CHRONIC GRANULOMATOUS DISEASE", "McLeod syndrome with chronic granulomatous disease", "McLeod syndrome with or without chronic granulomatous disease", "mcleod syndrome with or without chronic granulomatous disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "McLeod neuroacanthocytosis syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C4288933", "names": ["Secondary PHA due to UTI", "Mineralocorticoid Resistance due to UTI", "Hyponatremic Mineralocorticoid Resistance due to Urinary Tract Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyponatremic Mineralocorticoid Resistance due to Urinary Tract Infection", "shortest_name_length": 24}
{"curie": "UMLS:C0162848", "names": ["Lichenoid eruption", "Lichenoid Eruption", "lichenoid reaction", "Lichenoid reaction", "Eruption lichenoid", "Eruption, Lichenoid", "lichenoid reactions", "lichenoid eruptions", "Lichenoid Eruptions", "DERMATITIS LICHENOID", "LICHENOID DERMATITIS", "Lichenoid dermatitis", "Dermatitis lichenoid", "Licheniform Eruption", "lichenoid dermatitis", "Eruptions, Lichenoid", "Lichenoid dermatitis,", "Licheniform Eruptions", "Eruption, Licheniform", "Eruptions, Licheniform", "eruption; skin, lichenoid", "skin; eruption, lichenoid", "Lichen planus-like eruption", "Lichen planus-like dermatitis", "LICHEN PLANUS-LIKE DERMATITIS", "Dermatitis lichen planus-like"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lichenoid Eruptions", "shortest_name_length": 18}
{"curie": "UMLS:C5419451", "names": ["Advanced Transitional Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Transitional Cell Carcinoma", "shortest_name_length": 36}
{"curie": "MONDO:0032663", "names": ["DEE70", "EIEE70", "early infantile epileptic encephalopathy 70", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 70", "developmental and epileptic encephalopathy 70", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 70", "epileptic encephalopathy, early infantile, 70", "developmental and epileptic encephalopathy, 70"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 70", "shortest_name_length": 5}
{"curie": "UMLS:C1336186", "names": ["Stage IIB Lung Cancer", "Stage IIB Lung Carcinoma", "Stage IIB Carcinoma of Lung", "Stage IIB Lung Cancer AJCC v7", "Stage IIB Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Lung Cancer AJCC v7", "shortest_name_length": 21}
{"curie": "UMLS:C4331332", "names": ["Stage IV Hypopharyngeal Throat Cancer", "Stage IV Hypopharyngeal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Hypopharyngeal Carcinoma AJCC v8", "shortest_name_length": 37}
{"curie": "MONDO:0011757", "names": ["BDA1B", "brachydactyly type A1B", "BRACHYDACTYLY, TYPE A1, B", "brachydactyly, type A1, B", "Brachydactyly, Type A1, B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly type A1B", "shortest_name_length": 5}
{"curie": "MONDO:0016951", "names": ["partial trisomy/tetrasomy of chromosome 18p", "partial duplication/triplication of chromosome 18p", "partial trisomy/tetrasomy of the short arm of chromosome 18", "partial trisomy/tetrasomy of the short arm of chromosome type 18", "partial duplication/triplication of the short arm of chromosome 18"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial trisomy/tetrasomy of the short arm of chromosome 18", "shortest_name_length": 43}
{"curie": "UMLS:C3852985", "names": ["Occlusive Mesenteric Arterial Ischemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Occlusive Mesenteric Arterial Ischemia", "shortest_name_length": 38}
{"curie": "UMLS:C4329280", "names": ["Advanced Head and Neck Cancer", "Advanced Head and Neck Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Head and Neck Carcinoma", "shortest_name_length": 29}
{"curie": "UMLS:C1335125", "names": ["OPMDs", "Oral Potentially Malignant Disorders", "Oral Cavity and Lip Precancerous Condition", "Oral Cavity and Lip Premalignant Condition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral Cavity and Lip Precancerous Condition", "shortest_name_length": 5}
{"curie": "MONDO:0017884", "names": ["PRCC", "RCCP", "HPRCC", "RCCP1", "chromophil RCC", "renal adenocarcinoma", "papillary kidney carcinoma", "papillary renal cell cancer", "Papillary Renal Cell Cancer", "papillary renal cell carcinoma", "chromophil carcinoma of kidney", "Chromophil Carcinoma of Kidney", "Papillary Renal Cell Carcinoma", "Papillary renal cell carcinoma", "Chromophil carcinoma of kidney", "chromophil renal cell carcinoma", "Chromophil Renal Cell Carcinoma", "Renal Cell Carcinoma, Papillary", "chromophil carcinoma of the kidney", "renal cell carcinoma, papillary, 1", "Chromophil Carcinoma of the Kidney", "papillary renal cell adenocarcinoma", "Papillary renal cell adenocarcinoma", "Sporadic Papillary Renal Cell Carcinoma", "renal cell carcinoma, papillary, type 1", "sporadic papillary renal cell carcinoma", "Papillary renal cell carcinoma, familial", "Papillary renal cell carcinoma, sporadic", "Papillary renal cell carcinoma (disorder)", "Papillary renal cell carcinoma (diagnosis)", "papillary (chromophil) renal cell carcinoma", "Papillary (Chromophil) Renal Cell Carcinoma", "papillary renal carcinoma, malignant - (subtype)", "papillary renal cell carcinoma, multiple - (subtype)", "papillary renal cell carcinoma, familial - (subtype)", "papillary renal cell carcinoma, sporadic - (subtype)", "papillary renal cell carcinoma, bilateral - (subtype)", "Papillary renal cell carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papillary renal cell carcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0018183", "names": ["Staphylococcal necrotizing pneumonia", "Staphylococcal necrotising pneumonia", "staphylococcal necrotizing pneumonia", "necrotizing pneumonia due to Panton-Valentine leukocidin-producing Staphylococcus aureus", "Necrotizing pneumonia caused by Panton-Valentine leukocidin producing Staphylococcus aureus", "Necrotising pneumonia caused by Panton-Valentine leukocidin producing Staphylococcus aureus", "necrotizing pneumonia due to Panton-Valentine leukocidin-producing Staphylococcus aureus (diagnosis)", "Necrotizing pneumonia caused by Panton-Valentine leukocidin producing Staphylococcus aureus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "staphylococcal necrotizing pneumonia", "shortest_name_length": 36}
{"curie": "MONDO:0013510", "names": ["CMM6", "melanoma, cutaneous malignant, 6", "susceptibility to cutaneous malignant melanoma 6", "MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 6", "melanoma, cutaneous malignant, susceptibility to, 6", "melanoma, cutaneous malignant, susceptibility to, type 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melanoma, cutaneous malignant, susceptibility to, 6", "shortest_name_length": 4}
{"curie": "UMLS:C1521845", "names": ["Malignant Lymphoma, Large Cell, Cleaved and Non-Cleaved"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Lymphoma, Large Cell, Cleaved and Non-Cleaved", "shortest_name_length": 55}
{"curie": "UMLS:C0855100", "names": ["stage III small lymphocytic lymphoma", "Small Lymphocytic Lymphoma Stage III", "Stage III Small Lymphocytic Lymphoma", "small lymphocytic lymphoma, stage III", "B-cell small lymphocytic lymphoma stage III", "B-Cell Small Lymphocytic Lymphoma Stage III", "Stage III B-Cell Small Lymphocytic Lymphoma", "Ann Arbor Stage III Small Lymphocytic Lymphoma", "Small lymphocyte B lymphoma (Lukes-Collins Classification) stage III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-cell small lymphocytic lymphoma stage III", "shortest_name_length": 36}
{"curie": "MONDO:0016229", "names": ["genetic vascular anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genetic vascular anomaly", "shortest_name_length": 24}
{"curie": "UMLS:C0280744", "names": ["Previously Treated Myelodysplastic Syndrome", "previously treated myelodysplastic syndrome", "previously treated myelodysplastic syndromes", "myelodysplastic syndromes, previously treated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Previously Treated Myelodysplastic Syndrome", "shortest_name_length": 43}
{"curie": "MONDO:0019839", "names": ["panhypophysitis", "Infundibulo-panhypophysitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "panhypophysitis", "shortest_name_length": 15}
{"curie": "MONDO:0005094", "names": ["Perithelioma", "perithelioma", "hemangiopericytoma", "Hemangiopericytoma", "haemangiopericytoma", "Haemangiopericytoma", "Hemangiopericytomas", "Solitary fibrous tumor", "Hemangiopericytoma NOS", "Hemangiopericytoma, NOS", "Haemangiopericytoma NOS", "Solitary fibrous tumour", "HPA - hemangiopericytoma", "Haemangiopericytoma, NOS", "HPA - Hemangiopericytoma", "HPA - Haemangiopericytoma", "HPA - haemangiopericytoma", "malignant hemangiopericytoma", "hemangiopericytoma, malignant", "haemangiopericytic meningioma", "Hemangiopericytoma (disorder)", "Haemangiopericytic meningioma", "hemangiopericytoma (diagnosis)", "haemangiopericytic meningioma [obs]", "hemangiopericytoma, malignant (morphologic abnormality)", "neoplasm - soft tissue uncertain behavior blood vessel hemangiopericytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemangiopericytoma", "shortest_name_length": 12}
{"curie": "UMLS:C4527058", "names": ["Clinical Stage I Merkel Cell Carcinoma AJCC v8", "Clinical Stage I Neuroendocrine Carcinoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage I Merkel Cell Carcinoma AJCC v8", "shortest_name_length": 46}
{"curie": "UMLS:C0262516", "names": ["Stage IIA Hodgkin Lymphoma", "Hodgkin's Disease Stage IIA", "Stage IIA Hodgkin's Disease", "HODGKIN'S DISEASE STAGE IIA", "Stage IIA Hodgkin's Lymphoma", "Hodgkin's Lymphoma Stage IIA", "Ann Arbor Stage IIA Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage IIA Hodgkin Lymphoma", "shortest_name_length": 26}
{"curie": "UMLS:C0279971", "names": ["Stage I Ovarian Germ Cell Tumor", "stage I ovarian germ cell tumor", "ovarian germ cell tumor, stage I", "germ cell tumor, ovarian, stage I", "Stage I Ovarian Germ Cell Tumor AJCC v7", "Stage I Ovarian Germ Cell Tumor AJCC v6", "Stage I Malignant Germ Cell Tumor of Ovary", "Stage I Malignant Ovarian Germ Cell Neoplasm", "Stage I Malignant Germ Cell Neoplasm of Ovary", "Stage I Malignant Germ Cell Tumor of the Ovary", "Stage I Ovarian Germ Cell Tumor AJCC v6 and v7", "Stage I Malignant Germ Cell Neoplasm of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Ovarian Germ Cell Tumor AJCC v6 and v7", "shortest_name_length": 31}
{"curie": "MONDO:0018712", "names": ["CHE", "Composite hemangioendothelioma", "composite hemangioendothelioma", "Composite Hemangioendothelioma", "Composite haemangioendothelioma", "adult composite hemangioendothelioma", "Composite hemangioendothelioma (disorder)", "Composite hemangioendothelioma (diagnosis)", "Composite hemangioendothelioma (morphologic abnormality)", "neoplasm - soft tissue blood vessel hemangioendothelioma composite"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "composite hemangioendothelioma", "shortest_name_length": 3}
{"curie": "UMLS:C0154738", "names": ["Lumbosacral root lesion", "lumbosacral root lesion", "lumbosacral root lesions", "LUMBOSACRAL RADICULOPATHY", "Lumbosacral radiculopathy", "lumbosacral radiculopathy", "lesion; lumbosacral, root", "Lumbosacral root lesion, NOS", "Lumbosacral radiculopathy, NOS", "Radiculopathy, lumbosacral region", "radiculopathy of lumbosacral region", "Lumbosacral radiculopathy (disorder)", "lumbosacral root lesions (diagnosis)", "radiculopathy of lumbosacral region (diagnosis)", "nerve root and plexus disorder lumbosacral root lesions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lumbosacral radiculopathy", "shortest_name_length": 23}
{"curie": "MONDO:0016874", "names": ["partial monosomy of chromosome 9", "partial deletion of chromosome 9", "partial deletion of chromosome type 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of chromosome 9", "shortest_name_length": 32}
{"curie": "UMLS:C1334280", "names": ["Invasive Breast Papillary Carcinoma", "Invasive Papillary Breast Carcinoma", "Invasive papillary breast carcinoma", "Infiltrating Papillary Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Invasive papillary breast carcinoma", "shortest_name_length": 35}
{"curie": "MONDO:0009632", "names": ["Microphthalmia With Hyperopia, Retinal Degeneration, Macrophakia, And Dental Anomalies", "MICROPHTHALMIA WITH HYPEROPIA, RETINAL DEGENERATION, MACROPHAKIA, AND DENTAL ANOMALIES", "microphthalmia with hyperopia, retinal degeneration, macrophakia, and dental anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microphthalmia with hyperopia, retinal degeneration, macrophakia, and dental anomalies", "shortest_name_length": 86}
{"curie": "MONDO:0017422", "names": ["fingers absent", "adactyly of hand"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adactyly of hand", "shortest_name_length": 14}
{"curie": "MONDO:0008271", "names": ["PPD3", "polydactyly, preaxial 3", "Index Finger Polydactyly", "INDEX FINGER POLYDACTYLY", "index finger polydactyly", "Polydactyly, Preaxial III", "POLYDACTYLY, PREAXIAL III", "polydactyly, preaxial III", "preaxial polydactyly type 3", "Polydactyly of index finger", "Preaxial polydactyly type 3", "polydactyly, preaxial type 3", "polydactyly of an index finger", "Polydactyly of an index finger", "PPD3- preaxial polydactyly type 3", "Polydactyly of index finger (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polydactyly of an index finger", "shortest_name_length": 4}
{"curie": "MONDO:0020799", "names": ["Basal Cell Tumor", "basal cell tumor", "Basal cell tumor", "basal cell neoplasm", "Basal Cell Neoplasm", "neoplasm, basal cell", "Basal Cell Neoplasms", "Neoplasms, Basal Cell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "basal cell neoplasm", "shortest_name_length": 16}
{"curie": "MONDO:0008439", "names": ["SPEMR", "spemr", "spastic paraplegia epilepsy mental retardation", "Spastic paraplegia epilepsy mental retardation", "spastic paraplegia epilepsy intellectual disability", "SPASTIC PARAPLEGIA, EPILEPSY, AND MENTAL RETARDATION", "Spastic Paraplegia, Epilepsy, And Mental Retardation", "spastic paraplegia, epilepsy, and mental retardation", "spastic paraplegia, epilepsy, and intellectual disability", "spastic paraplegia-epilepsy-intellectual disability syndrome", "Spastic Paraplegia, Epilepsy, And Intellectual Development Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic paraplegia-epilepsy-intellectual disability syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0854798", "names": ["Relapsed Hepatoblastoma", "Recurrent Hepatoblastoma", "Hepatoblastoma recurrent", "Hepatoblastoma, Recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatoblastoma recurrent", "shortest_name_length": 23}
{"curie": "MONDO:0020402", "names": ["congenital accessory mitral valve tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital accessory mitral valve tissue", "shortest_name_length": 40}
{"curie": "MONDO:0018341", "names": ["Del(3)(q27.3)", "3q27.3 microdeletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "3q27.3 microdeletion syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0013866", "names": ["CLN11", "CLN11 disease", "neuronal ceroid lipofuscinosis 11", "Grn neuronal ceroid lipofuscinosis", "GRN neuronal ceroid lipofuscinosis", "CEROID LIPOFUSCINOSIS, NEURONAL, 11", "ceroid lipofuscinosis, neuronal, 11", "neuronal ceroid lipofuscinosis type 11", "Neuronal Ceroid Lipofuscinosis Type 11", "ceroid lipofuscinosis, neuronal, type 11", "neuronal ceroid lipofuscinosis caused by mutation in Grn", "neuronal ceroid lipofuscinosis caused by mutation in GRN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuronal ceroid lipofuscinosis 11", "shortest_name_length": 5}
{"curie": "MONDO:0011613", "names": ["PARK6", "Parkinson's disease 6", "PINK1 Parkinson disease", "early-onset Parkinson disease 6", "Parkinson Disease 6, Early-Onset", "Parkinson disease 6, early-onset", "Parkinson Disease 6, Early Onset", "PARKINSON DISEASE 6, EARLY-ONSET", "Parkinson disease 6, early onset", "Parkinson disease caused by mutation in PINK1", "PARKINSON DISEASE 6, LATE-ONSET, SUSCEPTIBILITY TO", "Parkinson disease 6, late-onset, susceptibility to", "autosomal recessive early-onset Parkinson disease 6", "Parkinson disease 6, autosomal recessive early-onset", "PARKINSON DISEASE 6, AUTOSOMAL RECESSIVE EARLY-ONSET", "Parkinson Disease 6, Autosomal Recessive Early-Onset", "autosomal recessive early-onset Parkinson's disease 6", "autosomal recessive early-onset Parkinson disease type 6", "PARKINSON DISEASE, AUTOSOMAL RECESSIVE EARLY-ONSET, DIGENIC, PINK1/DJ1", "Parkinson Disease, Autosomal Recessive Early-Onset, Digenic, Pink1-Dj1", "Parkinson disease, autosomal recessive early-onset, digenic, Pink1/Dj1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive early-onset Parkinson disease 6", "shortest_name_length": 5}
{"curie": "MONDO:0016540", "names": ["congenital secondary polycythemia", "congenital secondary erythrocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital secondary polycythemia", "shortest_name_length": 33}
{"curie": "UMLS:C4528635", "names": ["Stage III Acral Melanoma AJCC v7", "Stage III Acral Lentiginous Melanoma", "Stage III Acral Lentiginous Melanoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Acral Lentiginous Melanoma AJCC v7", "shortest_name_length": 32}
{"curie": "MONDO:0010184", "names": ["cblC", "MAHCC", "cblC defect", "cobalamin C defect", "cobalamin c disease", "Cobalamin C deficiency", "cobalamin C deficiency", "cblC - cobalamin locus c", "cobalamin locus c variant", "cblC methylmalonic acidemia and homocystinuria", "methylmalonic aciduria and homocystinuria cblC", "methylmalonic acidemia and homocystinuria cblC", "methylmalonic aciduria and homocystinuria type cblC", "methylmalonic aciduria and homocystinuria, cblC type", "Methylmalonic Aciduria and Homocystinuria, cblC Type", "methylmalonic acidemia and homocystinuria, cblC type", "methylmalonic acidemia with homocystinuria type cblC", "methylmalonic aciduria with homocystinuria, type cblC", "methylmalonic acidemia with homocystinuria, type cblC", "methylmalonic aciduria and homocystinuria, cblC type, digenic", "METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE, DIGENIC", "methylmalonic aciduria and homocystinuria, vitamin B12-responsive", "combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblC", "vitamin B12 metabolic defect with combined deficiency of methylmalonyl-Coa mutase and homocysteine:methyltetrahydrofolate methyltransferase"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "methylmalonic aciduria and homocystinuria type cblC", "shortest_name_length": 4}
{"curie": "MONDO:0020344", "names": ["postsynaptic congenital myasthenic syndrome", "postsynaptic congenital myasthenic syndromes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postsynaptic congenital myasthenic syndrome", "shortest_name_length": 43}
{"curie": "MONDO:0011633", "names": ["CMT2C", "HMSN2C", "CMT 2C", "HMSN 2C", "HMSN IIC", "HMSN 2 C", "Charcot-Marie-Tooth disease type 2C", "Charcot Marie Tooth disease type 2C", "Charcot-Marie-Tooth neuropathy type 2C", "Charcot-Marie-Tooth neuropathy, type 2C", "Charcot-Marie-Tooth Neuropathy, Type 2C", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2C", "TRPV4 Charcot-Marie-Tooth disease type 2", "Charcot-Marie-Tooth disease axonal type 2C", "hereditary motor and sensory neuropathy 2 C", "Charcot-Marie-Tooth disease, axonal, type 2C", "hereditary motor and sensory neuropathy, type 2C", "hereditary motor and sensory neuropathy type IIc", "HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC", "Hereditary Motor And Sensory Neuropathy, Type IIC", "hereditary motor and sensory neuropathy, type IIC", "autosomal dominant Charcot-Marie-Tooth disease type 2C", "Autosomal dominant Charcot-Marie-Tooth disease type 2C", "HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC (disorder)", "autosomal cominant axonal Charcot-Marie-Tooth disease type 2C", "Charcot-Marie-Tooth disease type 2 caused by mutation in TRPV4", "Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2C", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2C", "Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2C", "Autosomal dominant Charcot-Marie-Tooth disease type 2C (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease axonal type 2C", "shortest_name_length": 5}
{"curie": "MONDO:0024905", "names": ["bird disease", "Bird Disease", "disease, Bird", "Bird Diseases", "Avian Disease", "Disease, Bird", "avian disease", "birds disease", "Avian disease", "bird diseases", "Avian Diseases", "diseases, Bird", "avian diseases", "Diseases, Bird", "Disease, Avian", "disease, Avian", "birds diseases", "Avian diseases", "Diseases, Avian", "Birds--Diseases", "diseases, Avian"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bird disease", "shortest_name_length": 12}
{"curie": "MONDO:0011721", "names": ["DMAT", "distal anterior compartment myopathy", "Distal anterior compartment myopathy", "Distal myopathy with anterior tibial onset", "distal myopathy with anterior tibial onset", "Myopathy, Distal, with Anterior Tibial Onset", "myopathy, distal, with anterior tibial onset", "MYOPATHY, DISTAL, WITH ANTERIOR TIBIAL ONSET", "distal muscular dystrophy with anterior tibial onset", "Distal myopathy with anterior tibial onset (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal myopathy with anterior tibial onset", "shortest_name_length": 4}
{"curie": "MONDO:0014257", "names": ["NPHS9", "COQ8B nephrotic syndrome", "nephrotic syndrome type 9", "nephrotic syndrome, type 9", "NEPHROTIC SYNDROME, TYPE 9", "nephrotic syndrome caused by mutation in COQ8B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrotic syndrome, type 9", "shortest_name_length": 5}
{"curie": "MONDO:0013639", "names": ["NRCLP6", "narcolepsy 6", "NARCOLEPSY 6, SUSCEPTIBILITY TO", "narcolepsy 6, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "narcolepsy 6, susceptibility to", "shortest_name_length": 6}
{"curie": "MONDO:0005380", "names": ["BONE INFARCT", "bone infarct", "Bone Necroses", "Bone Necrosis", "Bone necrosis", "NECROSIS BONE", "Osteonecroses", "OSTEONECROSIS", "Necrosis;bone", "bone necrosis", "Necrosis bone", "osteonecrosis", "bone infarcts", "BONE NECROSIS", "Osteonecrosis", "Necrosis, Bone", "bone; necrosis", "necrosis; bone", "Necroses, Bone", "bone infarction", "Bones--Necrosis", "Bone infarction", "Bone Infarction", "necrosis of bone", "Aseptic necrosis", "ASEPTIC NECROSIS", "Necrosis;aseptic", "Aseptic Necrosis", "aseptic necrosis", "Necrosis of bone", "Necrosis, aseptic", "Avascular necrosis", "Osteochondronecrosis", "Necrosis of bone NOS", "ASEPTIC NECROSIS BONE", "aseptic bone necrosis", "Aseptic bone necrosis", "Aseptic necrosis bone", "Bone Aseptic Necrosis", "ischemic bone disease", "ASEPTIC BONY NECROSIS", "Ischemic bone necrosis", "aseptic; bone necrosis", "necrosis; bone, aseptic", "Ischaemic bone necrosis", "aseptic necrosis of bone", "Bone necrosis (disorder)", "Aseptic Necrosis of Bone", "Aseptic necrosis of bone", "Unspecified osteonecrosis", "Aseptic necrosis of talus", "Avascular necrosis of bone", "HUMERUS AVASCULAR NECROSIS", "Necrosis, Aseptic, of Bone", "Osteonecrosis, unspecified", "osteochondrosis; upper limb", "upper limb; osteochondrosis", "aseptic necrosis of humerus", "limb; osteochondrosis, upper", "osteochondrosis; limb, upper", "aseptic necrosis (diagnosis)", "Avascular Necrosis of Humerus", "Osteochondrosis of upper limb", "HUMERUS HEAD ASEPTIC NECROSIS", "Aseptic necrosis of bone (disorder)", "Aseptic Necrosis of Head of Humerus", "Aseptic necrosis of head of humerus", "Aseptic necrosis of talus (disorder)", "Juvenile osteochondrosis of upper limb", "osteochondrosis; juvenile, limb, upper", "Osteochondrosis of upper extremity NOS", "aseptic necrosis of talus due to drugs", "aseptic necrosis of humerus (diagnosis)", "Aseptic necrosis of bone, site unspecified", "Aseptic necrosis of head and neck of femur", "Aseptic Necrosis of Head and Neck of Femur", "Aseptic necrosis of medial femoral condyle", "Aseptic necrosis (morphologic abnormality)", "juvenile osteochondrosis of upper extremity", "Juvenile osteochondrosis of upper extremity", "Death of bone due to decreased blood supply", "Aseptic necrosis of bone of unspecified site", "Aseptic necrosis of head AND/OR neck of femur", "Aseptic necrosis of head and/or neck of femur", "Aseptic necrosis of head of humerus (disorder)", "Juvenile osteochondrosis of upper extremity NOS", "Juvenile osteochondrosis of upper extremity, NOS", "aseptic necrosis of talus due to drugs (diagnosis)", "Aseptic necrosis of medial femoral condyle (disorder)", "Juvenile osteochondrosis of upper extremity (disorder)", "juvenile osteochondrosis of upper extremity (diagnosis)", "aseptic necrosis of medial femoral condyle due to drugs", "Aseptic necrosis of head AND/OR neck of femur (disorder)", "aseptic necrosis of medial femoral condyle due to drugs (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteonecrosis", "shortest_name_length": 12}
{"curie": "MONDO:0007835", "names": ["Intususception", "intussuception", "intususception", "Intususceptions", "INTUSSUSCEPTION", "intussusception", "introsusception", "Intussusception", "Introsusception", "intussusceptions", "Intussusceptions", "ISN - Intussusception", "bowel intussusception", "Intestinal Invagination", "Intestinal Invaginations", "intussusception of bowel", "Intussusception of bowel", "Invagination, Intestinal", "Invaginations, Intestinal", "Invagination of intestine", "Invagination of intestines", "intestinal intussusception", "Intestinal intussusception", "Intestines--Intussusception", "intussusception (diagnosis)", "Intussusception of intestine", "intussusception of intestine", "Intussusception of the intestine", "Invagination of intestine or colon", "invagination of intestine or colon", "Intussusception of intestine (disorder)", "intussusception (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intussusception", "shortest_name_length": 14}
{"curie": "UMLS:C0024668", "names": ["Experimental Mammary Neoplasm", "Experimental Mammary Neoplasms", "Mammary Neoplasm, Experimental", "Neoplasm, Experimental Mammary", "Neoplasms, Experimental Mammary", "Mammary Neoplasms, Experimental"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mammary Neoplasms, Experimental", "shortest_name_length": 29}
{"curie": "UMLS:C0087086", "names": ["THROMBI", "Thrombi", "thrombi", "thrombus", "Thrombus", "Blood Clot", "blood clot", "Thrombotic", "Clot, Blood", "Blood Clots", "Clots, Blood", "Thrombus, NOS", "Thrombus (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thrombus", "shortest_name_length": 7}
{"curie": "MONDO:0015872", "names": ["giant adenofibroma of the breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "giant adenofibroma of the breast", "shortest_name_length": 32}
{"curie": "MONDO:0034895", "names": ["serpentine-like syndrome", "congenital brachyesophagus-intrathoracic stomach-vertebral anomalies syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital brachyesophagus-intrathoracic stomach-vertebral anomalies syndrome", "shortest_name_length": 24}
{"curie": "UMLS:C5238831", "names": ["Other", "Other Genetic Syndrome Associated with Congenital Heart Defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Other Genetic Syndrome Associated with Congenital Heart Defect", "shortest_name_length": 5}
{"curie": "MONDO:0005895", "names": ["Paragonimosis", "Paragonimiasis", "Paragonimiases", "PARAGONIMIASIS", "paragonimiasis", "Lung fluke disease", "lung fluke disease", "Endemic hemoptysis", "HEMOPTYSIS, ENDEMIC", "Endemic haemoptysis", "fluke disease; lung", "lung; fluke disease", "Lung fluke infection", "lung; disease, fluke", "lung fluke infection", "Paragonimus Infection", "Pulmonary distomiasis", "DISTOMIASIS, PULMONARY", "Paragonimus Infections", "Infection, Paragonimus", "Pulmonary distomatosis", "Infections, Paragonimus", "Paragonimus; infestation", "pulmonary paragonimiasis", "Infection by Paragonimus", "infestation; Paragonimus", "infection by Paragonimus", "Pulmonary paragonimiasis", "paragonimiasis (diagnosis)", "Oriental lung fluke disease", "Endemic oriental hemoptysis", "lung fluke disease; oriental", "Endemic oriental haemoptysis", "LUNG FLUKE DISEASE, ORIENTAL", "oriental; lung fluke disease", "Infection by Paragonimus, NOS", "lung; disease, fluke, oriental", "Infection caused by Paragonimus", "Paragonimus westermani Infection", "Paragonimus westermani infection", "Infection, Paragonimus westermani", "Paragonimus westermani Infections", "disease (or disorder); lung, fluke", "Infections, Paragonimus westermani", "infestation; fluke, lung (oriental)", "fluke; infestation, lung (oriental)", "pulmonary paragonimiasis (diagnosis)", "Paragonimus westermani infectious disease", "Paragonimus westermani disease or disorder", "Infection caused by Paragonimus (disorder)", "disease (or disorder); lung, fluke, oriental", "Paragonimus westermani caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paragonimiasis", "shortest_name_length": 13}
{"curie": "UMLS:C0854850", "names": ["Mycosis fungoides refractory", "Refractory Mycosis Fungoides", "Mycosis Fungoides Refractory"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mycosis fungoides refractory", "shortest_name_length": 28}
{"curie": "UMLS:C1336173", "names": ["Stage IIA Squamous Cell Lung Cancer", "Stage IIA Squamous Cell Lung Carcinoma", "Stage IIA Squamous Cell Carcinoma of Lung", "Stage IIA Squamous Cell Carcinoma of the Lung", "Stage IIA Squamous Cell Lung Carcinoma AJCC v7", "Stage IIA Lung Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Lung Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 35}
{"curie": "MONDO:0011367", "names": ["acrodysplasia with ossification abnormalities, short stature and fibular hypoplasia", "Acrodysplasia with ossification abnormalities, short stature, and fibular hypoplasia", "ACRODYSPLASIA WITH OSSIFICATION ABNORMALITIES, SHORT STATURE, AND FIBULAR HYPOPLASIA", "acrodysplasia with ossification abnormalities, short stature, and fibular hypoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acrodysplasia with ossification abnormalities, short stature, and fibular hypoplasia", "shortest_name_length": 83}
{"curie": "MONDO:0009793", "names": ["OFD3", "Ofds 3", "OFDS III", "OFD syndrome 3", "Sugarman syndrome", "SUGARMAN SYNDROME", "Orofaciodigital syndrome 3", "orofaciodigital syndrome 3", "OROFACIODIGITAL SYNDROME III", "orofaciodigital syndrome III", "Orofaciodigital syndrome III", "digito-orofacial syndrome III", "Orofacial-digital syndrome III", "Oral-facial-digital syndrome 3", "oral facial digital syndrome 3", "orofaciodigital syndrome type 3", "Orofaciodigital syndrome type 3", "oral-facial-digital syndrome III", "orofaciodigital syndrome type III", "orofaciodigital (OFD) syndrome III", "oral-facial-digital syndrome type 3", "oral facial digital syndrome type 3", "Oral-facial-digital syndrome type 3", "oral-Facial-digital syndrome, type 3", "Oral-Facial-Digital Syndrome, Type III", "ORAL-FACIAL-DIGITAL SYNDROME, TYPE III", "OFD III - Orofacial-digital syndrome III", "Orofacial-digital syndrome III (disorder)", "Brachydactyly of the hands and feet with duplication of the first toes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orofaciodigital syndrome III", "shortest_name_length": 4}
{"curie": "MONDO:0011348", "names": ["polydactylia", "Extra digits", "isolated polydactyly", "supernumerary digits", "nonsyndromic polydactyly", "non-syndromic polydactyly", "isolated polydactyly (disease)", "nonsyndromic polydactyly (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-syndromic polydactyly", "shortest_name_length": 12}
{"curie": "MONDO:0002329", "names": ["testis disease", "Testis disorder", "disorder testes", "testis disorder", "TESTIS DISORDER", "testes disorders", "Testes Disorders", "testis; disorder", "Testis--Diseases", "disorders testes", "disease of testis", "DISORDER TESTICLE", "Disease of testis", "Disorder testicle", "disorders testicle", "Diseases of Testis", "Testicular Disease", "disorder of testis", "Testicular disease", "testicular disease", "disease testicular", "Disorder of testis", "Testicular Disorder", "Disease, Testicular", "disorders testicles", "Testicular disorder", "testicular diseases", "Testicular Diseases", "testicular disorder", "TESTICULAR DISORDER", "disorders testicular", "testicular disorders", "Testicular Disorders", "Diseases, Testicular", "Disease of testis, NOS", "Disorder of testis, NOS", "Testicular disorder NOS", "Testicular disorder, NOS", "testis disease or disorder", "disease or disorder of testis", "disease (or disorder); testis", "Disorder of testis (disorder)", "disorder of testis (diagnosis)", "Disorder of testis and epididymis", "testis (excluding endocrine function)", "DISEASES OF THE TESTES AND EPIDIDYMIDES", "Disorder of testis and epididymis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular disorder", "shortest_name_length": 14}
{"curie": "UMLS:C4725615", "names": ["Recurrent Ovarian Endometrioid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Ovarian Endometrioid Adenocarcinoma", "shortest_name_length": 45}
{"curie": "MONDO:0009071", "names": ["renal hypouricemia", "Renal hypouricemia", "hypouricemia, renal", "Dalmatian hypouricemia", "Familial renal hypouricemia", "Familial renal hypouricaemia", "hereditary renal hypouricemia", "Familial renal hypouricemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary renal hypouricemia", "shortest_name_length": 18}
{"curie": "UMLS:C5205874", "names": ["RENAL RADIATION INJURY", "Renal Radiation Injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal Radiation Injury", "shortest_name_length": 22}
{"curie": "MONDO:0009938", "names": ["pulmonic stenosis", "pulmonary stenosis", "valvular pulmonic stenosis", "pulmonic stenosis (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonic stenosis", "shortest_name_length": 17}
{"curie": "UMLS:C1336509", "names": ["Storiform-Pleomorphic Malignant Fibrous Histiocytoma NCI Grade 3", "Storiform-Pleomorphic Malignant Fibrous Histiocytoma NCI Grade III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Storiform-Pleomorphic Malignant Fibrous Histiocytoma NCI Grade 3", "shortest_name_length": 64}
{"curie": "MONDO:0009047", "names": ["Cryptorchid", "cryptorchism", "Cryptorchism", "CRYPTORCHISM", "cryptorchidism", "Cryptorchidism", "CRYPTORCHIDISM", "Cryptorchism NOS", "testes undescend", "Retained testicle", "maldescent; testis", "Undescended testis", "Undescended Testis", "UNDESCENDED TESTES", "Undescended Testes", "undescended testes", "Undescended testes", "UNDESCENDED TESTIS", "undescend testicle", "undescended testis", "Maldescended testis", "maldescended testis", "Testis, Undescended", "Testes, Undescended", "testicle; nondescent", "UNDESCENDED TESTICLE", "Undescended Testicle", "nondescent; testicle", "Testicle undescended", "Undescended testicle", "undescended testicle", "testicle undescended", "maldescent of testis", "Maldescent of testis", "Maldescended testicle", "Undescended testicles", "testicles undescended", "Testicle maldescended", "undescended testicles", "cryptorchidism (disease)", "UDT - Undescended testes", "Imperfectly descended testis", "Undescended testicle (disorder)", "undescended testicle (diagnosis)", "Undescended testicle, unspecified", "Undescended testicle/cryptorchism", "IDT - Imperfectly descended testis", "CRYPTORCHIDISM, UNILATERAL OR BILATERAL", "Cryptorchidism, Unilateral Or Bilateral", "Cryptorchidism, unilateral or bilateral", "cryptorchidism, unilateral or bilateral", "Cryptorchidism (unilateral or bilateral)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cryptorchidism", "shortest_name_length": 11}
{"curie": "MONDO:0007254", "names": ["breast ca", "breast tumor", "Breast Cancer", "Breast cancer", "breast cancer", "mammary tumor", "BREAST CANCER", "Breast--Cancer", "Mammary Cancer", "Cancer, Breast", "mammary cancer", "breast cancers", "Mammary Cancers", "Cancer, Mammary", "mammary neoplasm", "Cancers, Mammary", "Cancer of breast", "Cancer of Breast", "cancer of breast", "Breast cancer NOS", "BREAST CANCER NOS", "CA - Breast cancer", "Cancer of the Breast", "cancer of the breast", "primary breast cancer", "Malignant Breast Tumor", "malignant breast tumor", "Breast tumor malignant", "Breast Malignant Tumor", "Breast Malignant Tumors", "Breast tumour malignant", "breast malignant tumors", "malignant breast neoplasm", "Malignant tumor of breast", "Breast Malignant Neoplasm", "malignant tumor of breast", "Malignant Breast Neoplasm", "Malignant neoplasm breast", "Malignant breast neoplasm", "Malignant Tumor of Breast", "breast cancer (diagnosis)", "breast malignant neoplasm", "Malignant tumour of breast", "Breast Malignant Neoplasms", "Malignant neoplasm of breast", "malignant neoplasm of breast", "Malignant Neoplasm of Breast", "Malignant Tumor of the Breast", "malignant tumor of the breast", "Breast cancer stage unspecified", "Malignant Neoplasm of the Breast", "malignant neoplasm of the breast", "Malignant neoplasms of breast (C50)", "Malignant neoplasm of breast (disorder)", "malignant neoplasm of breast (diagnosis)", "Malignant neoplasm of breast, unspecified", "Malignant neoplasm of breast, unspecified part"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast cancer", "shortest_name_length": 9}
{"curie": "UMLS:C0435751", "names": ["open rib fracture", "Open fracture rib", "Open Fracture of Rib", "Open fracture of rib", "Open fracture of ribs", "Open fracture of rib(s)", "Fracture of rib(s), open", "Open fracture of rib, NOS", "open rib fracture (diagnosis)", "Open fracture of rib (disorder)", "Open fracture of rib, unspecified", "Open fracture of ribs, unspecified", "Open fracture of rib(s), unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Open fracture of rib", "shortest_name_length": 17}
{"curie": "MONDO:0035121", "names": ["Myeloid/lymphoid neoplasm with PCM1-JAK2", "myeloid/lymphoid neoplasms with PCM1-JAK2", "Myeloid/Lymphoid Neoplasms with PCM1-JAK2", "Myeloid/lymphoid neoplasms with PCM1-JAK2", "Myeloid/Lymphoid Neoplasm with JAK2-PCM1 Fusion", "Myeloid and/or lymphoid neoplasm with PCM1-JAK2", "Myeloid/Lymphoid Neoplasm with PCM1- JAK2 Fusion", "Myeloid/lymphoid neoplasm associated with JAK2 rearrangement", "myeloid/lymphoid neoplasm associated with JAK2 rearrangement", "Myeloid and Lymphoid Neoplasms with t(8;9)(p22;p24.1);PCM1-JAK2", "Myeloid and/or lymphoid neoplasm with pericentriolar material 1-janus kinase 2", "Myeloid and/or lymphoid neoplasm with pericentriolar material 1-janus kinase 2 (disorder)", "Myeloid and/or lymphoid neoplasm with pericentriolar material 1-janus kinase 2 (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myeloid/lymphoid neoplasm associated with JAK2 rearrangement", "shortest_name_length": 40}
{"curie": "MONDO:0008006", "names": ["MBS", "Möbius syndrome", "Möbius Syndrome", "Möbius Sequence", "MOBIUS SYNDROME", "Mobius Syndrome", "mobius syndrome", "Mobius syndrome", "Moebius Sequence", "MOEBIUS SYNDROME", "Moebius Spectrum", "Mobius Syndromes", "Moebius syndrome", "moebius syndrome", "Moebius sequence", "moebius sequence", "Moebius Syndrome", "Mobius' syndrome", "MOEBIUS SEQUENCE", "Moebius' syndrome", "Moebius' anomalad", "Moebius Syndromes", "Mobius II syndrome", "Moebius II syndrome", "Mobius' II syndrome", "Charlie M. syndrome", "Oculofacial paralysis", "paralysis; oculofacial", "oculofacial; paralysis", "MOBS - Moebius syndrome", "congenital facial diplegia", "CONGENITAL NUCLEAR APLASIA", "Congenital facial diplegia", "Facial Diplegia, Congenital", "Moebius syndrome (disorder)", "Moebius syndrome (diagnosis)", "Facial-limb disruptive spectrum", "Moebius syndrome, Isolated cases", "Hypoglossia-hypodactyly syndrome", "congenital oculofacial paralysis", "Congenital bilateral facial palsy", "Glossopalatine ankylosis syndrome", "PARALYSIS, OCULOFACIAL, CONGENITAL", "congenital facial diplegia syndrome", "CONGENITAL FACIAL DIPLEGIA SYNDROME", "Congenital bilateral facial weakness", "diplegia; facial, congenital syndrome", "syndrome; facial diplegia, congenital", "facial; diplegia, congenital syndrome", "Oromandibular-limb hypogenesis spectrum", "Oromandibular-Limb Hypogenesis Spectrum", "oromandibular-limb hypogenesis spectrum", "Moebius congenital oculofacial paralysis", "Moebius Congenital Oculofacial Paralysis", "Moebius; congenital oculofacial paralysis", "Congenital Oculofacial Paralysis, Moebius", "congenital; oculofacial paralysis, Moebius", "Congenital Ophthalmoplegia and Facial Paresis", "Oromandibular-limb hypogenesis spectrum (disorder)", "Congenital paralysis of 6th and 12th cranial nerves", "absence or underdevelopment of the 6th and 7th cranial nerves"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mobius syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C4682632", "names": ["Stage IIIA2 Fallopian Tube Cancer", "Stage IIIA2 Fallopian Tube Cancer AJCC v8", "Stage IIIA2 Fallopian Tube Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA2 Fallopian Tube Cancer AJCC v8", "shortest_name_length": 33}
{"curie": "MONDO:0000262", "names": ["OTOMYCOSIS", "otomycosis", "Otomycosis", "Otomycoses", "Singapore ear", "Otomycosis, NOS", "otomycosis externa", "Fungal otitis externa", "Otomycosis (disorder)", "Otitis externa fungal", "otitis mycotic externa", "Otitis mycotic externa", "otomycosis externa (diagnosis)", "otitis externa infective otomycosis", "external ear fungal infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "otomycosis", "shortest_name_length": 10}
{"curie": "UMLS:C0343378", "names": ["Nodular gastritis", "helicobacter gastritis", "Helicobacter Gastritis", "Helicobacter gastritis", "gastritis due to H. pylori", "helicobacter pylori gastritis", "Helicobacter pylori gastritis", "gastritis helicobacter pylori", "Helicobacter-associated gastritis", "gastritis due to H. pylori (diagnosis)", "Gastritis caused by Helicobacter pylori", "Helicobacter Pylori-Associated Gastritis", "Helicobacter pylori-associated gastritis", "Helicobacter-associated gastritis (disorder)", "Gastritis caused by Helicobacter pylori (disorder)", "Gastritis caused by H. pylori (Helicobacter pylori)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Helicobacter pylori-associated gastritis", "shortest_name_length": 17}
{"curie": "UMLS:C5418873", "names": ["Refractory Myeloproliferative Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Myeloproliferative Neoplasm", "shortest_name_length": 38}
{"curie": "MONDO:0002387", "names": ["Lias", "angiosarcoma liver", "liver angiosarcoma", "Liver Angiosarcoma", "angiosarcoma; liver", "liver; angiosarcoma", "Hepatic Angiosarcoma", "Hepatic angiosarcoma", "hepatic angiosarcoma", "Kupffer cell sarcoma", "angiosarcoma of liver", "Liver Hemangiosarcoma", "Angiosarcoma of liver", "liver hemangiosarcoma", "Angiosarcoma of Liver", "hepatic hemangiosarcoma", "Hepatic hemangiosarcoma", "Hepatic Hemangiosarcoma", "Hemangiosarcoma of Liver", "hemangiosarcoma of liver", "Hemangiosarcoma of liver", "Angiosarcoma of the Liver", "angiosarcoma of the liver", "Hemangiosarcoma of the Liver", "hemangiosarcoma of the liver", "hemangiosarcoma of the Liver", "liver angiosarcoma (disease)", "Primary angiosarcoma of liver", "primary angiosarcoma of liver", "Primary Angiosarcoma of Liver", "angiosarcoma (disease) of liver", "Angiosarcoma of liver (disorder)", "Primary Angiosarcoma of the Liver", "Angiosarcoma of liver (diagnosis)", "primary angiosarcoma of the liver", "Hemangiosarcoma of liver (disorder)", "hemangiosarcoma of liver (diagnosis)", "liver neoplasm malignant angiosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "liver angiosarcoma", "shortest_name_length": 4}
{"curie": "MONDO:0020708", "names": ["BAD", "FAS", "MIBS", "flail arm syndrome", "Flail Arm Syndrome", "Man-in-barrel Syndrome", "man-in-barrel syndrome", "Man-in-the-barrel syndrome", "Brachial Amyotrophic Diplegia", "brachial amyotrophic diplegia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachial amyotrophic diplegia", "shortest_name_length": 3}
{"curie": "MONDO:0025491", "names": ["fip", "FIP", "Feline Infectious Peritonitis", "feline infectious peritonitis", "Feline infectious peritonitis", "Peritonitis, Feline Infectious", "peritonitis, feline infectious", "Infectious Peritonitis, Feline", "infectious peritonitis, feline", "Peritonitis, Infectious, Feline", "feline infectious peritonitides", "peritonitis, infectious, feline", "Feline Infectious Peritonitides", "infectious peritonitides, feline", "Infectious Peritonitides, Feline", "Feline infectious peritonitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "feline infectious peritonitis", "shortest_name_length": 3}
{"curie": "UMLS:C4721929", "names": ["stage IVB uterine sarcoma", "Stage IVB Uterine Sarcoma", "stage IVB uterine sarcoma AJCC v7", "Stage IVB Uterine Sarcoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Uterine Sarcoma AJCC v7", "shortest_name_length": 25}
{"curie": "UMLS:C5670412", "names": ["Unresectable Fallopian Tube Endometrioid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Fallopian Tube Endometrioid Adenocarcinoma", "shortest_name_length": 55}
{"curie": "MONDO:0003723", "names": ["breast blunt duct adenosis", "Breast Blunt Duct Adenosis", "Blunt Duct Adenosis of Breast", "blunt duct adenosis of breast", "blunt duct adenosis of the breast", "Blunt Duct Adenosis of the Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blunt duct adenosis of breast", "shortest_name_length": 26}
{"curie": "MONDO:0001154", "names": ["manchurian typhus", "Manchurian typhus", "Siberian tick typhus", "NORTH ASIAN TICK FEVER", "North Asian tick fever", "Tick fever, North Asian", "North Asian; tick fever", "North Asian Tick Typhus", "North Asian tick typhus", "tick fever; North Asian", "spotted fever; North Asian", "North Asian; spotted fever", "Rickettsia sibirica spotted fever", "North Asian tick fever (diagnosis)", "North Asian tick typhus (disorder)", "spotted fever; Rickettsia sibirica", "rickettsiosis; Rickettsia sibirica", "Rickettsia; sibirica, spotted fever", "fever; North Asian tick-borne fever", "North Asian tick-borne fever; fever", "Tick fever due to Rickettsia siberica", "Spotted fever due to Rickettsia siberica", "Spotted fever due to Rickettsia sibirica", "spotted fever due to rickettsia siberica", "sibirica; Rickettsia sibirica, spotted fever", "North Asian tick fever (disorder) [ambiguous]", "spotted fever due to rickettsia siberica (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Siberian tick typhus", "shortest_name_length": 17}
{"curie": "UMLS:C2609162", "names": ["Periprosthetic Fracture", "Periprosthetic fracture", "Periprosthetic Fractures", "Fracture, Periprosthetic", "Fractures, Periprosthetic", "Fracture of bone adjacent to prosthesis", "Fracture of bone adjacent to prosthesis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Periprosthetic Fractures", "shortest_name_length": 23}
{"curie": "MONDO:0007212", "names": ["brachydactyly long thumb type", "Brachydactyly long thumb type", "Brachydactyly, Long-Thumb Type", "brachydactyly, long thumb type", "brachydactyly, long-thumb type", "BRACHYDACTYLY, LONG-THUMB TYPE", "Brachydactyly, long thumb type", "Brachydactyly-long thumb syndrome", "LONG-THUMB BRACHYDACTYLY SYNDROME", "Long thumb brachydactyly syndrome", "brachydactyly-long thumb syndrome", "long-thumb brachydactyly syndrome", "Long thumb brachydactyly syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly-long thumb syndrome", "shortest_name_length": 29}
{"curie": "UMLS:C0400807", "names": ["stress ulcer", "ulcer stress", "stress ulcers", "ulcers stress", "stress ulcer stomach", "Gastric stress ulcer", "Gastric Stress Ulcer", "stress stomach ulcer", "Stress ulcer of stomach", "Stress ulcers of stomach, NOS", "Stress ulcer of stomach (disorder)", "Acute gastric erosion associated with severe burns"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stress ulcer of stomach", "shortest_name_length": 12}
{"curie": "UMLS:C0344258", "names": ["Delle", "Corneal Delle", "Corneal dellen", "Corneal Dellen", "Corneal dellen (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Corneal dellen", "shortest_name_length": 5}
{"curie": "MONDO:0010103", "names": ["fused teeth", "Fused teeth", "Fused tooth", "Fused Teeth", "tooth fusion", "Joined teeth", "Double teeth", "TEETH, FUSED", "Double Tooth", "Teeth, Fused", "teeth, fused", "teeth fusion", "fusion; tooth", "tooth; fusion", "Tooth, Double", "Fusion of teeth", "fusion of teeth", "Connation of teeth", "tooth fusion (diagnosis)", "Fusion of teeth (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "teeth, fused", "shortest_name_length": 11}
{"curie": "MONDO:0013846", "names": ["PPCM, SUSCEPTIBILITY TO", "Ppcm, susceptibility to", "PERIPARTUM CARDIOMYOPATHY, SUSCEPTIBILITY TO", "peripartum cardiomyopathy, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peripartum cardiomyopathy, susceptibility to", "shortest_name_length": 23}
{"curie": "UMLS:C4055463", "names": ["Prenatal Hydronephrosis", "Antenatal Hydronephrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Antenatal Hydronephrosis", "shortest_name_length": 23}
{"curie": "MONDO:0000761", "names": ["microdeletion syndrome", "chromosomal deletion syndrome", "syndrome caused by partial chromosomal deletion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndrome caused by partial chromosomal deletion", "shortest_name_length": 22}
{"curie": "MONDO:0010626", "names": ["XHIM", "IHIS", "IMD3", "HIGM", "XHIGM", "HIGM1", "HIGMX-1", "HIGM1 Syndrome", "HIGM1 Syndromes", "HYPER-IgM SYNDROME", "hyper IgM syndrome", "immunodeficiency 3", "IMMUNODEFICIENCY 3", "hyper-IgM syndrome", "hyper-IgM syndrome 1", "HYPER-IgM SYNDROME 1", "Hyper-IgM Syndrome 1", "Hyper IgM Syndrome 1", "hyper IgM syndrome 1", "CD40 Ligand Deficiency", "CD40 ligand deficiency", "hyper-IgM syndrome type 1", "Hyper-IgM syndrome type 1", "X-Linked Hyper IgM Syndrome", "X-Linked Hyper-IgM Syndrome", "X-linked hyper-IgM syndrome", "X-linked hyper IgM syndrome", "X Linked Hyper IgM Syndrome", "hyper-IgM syndrome, X-linked", "hyperimmunoglobulin M syndrome", "X-Linked Hyper-IgM Immunodeficiency", "Hyper-IgM Immunodeficiency, X-Linked", "hyper IgM immunodeficiency, X-linked", "Immunodeficiency, X-Linked Hyper-IgM", "hyper-IgM immunodeficiency, X-linked", "HYPER-IgM IMMUNODEFICIENCY, X-LINKED", "Hyper IgM Immunodeficiency, X Linked", "X-Linked Hyper-IgM Immunodeficiencies", "Hyper-IgM Immunodeficiencies, X-Linked", "Immunodeficiencies, X-Linked Hyper-IgM", "immunodeficiency with hyper IgM type 1", "Immunodeficiency with Hyper-IgM, Type 1", "X-linked hyperimmunoglobulin M syndrome", "Immunodeficiency with Hyper IgM, Type 1", "IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 1", "immunodeficiency with hyper-IgM, type 1", "X-linked with hyper-IgM immunodeficiency", "X-linked immunodeficiency with hyper IgM", "X-linked immunodeficiency with hyper-IgM", "X-linked hyper-immunoglobulin M syndrome", "Hyper-IgM syndrome due to CD40L deficiency", "hyper-IgM syndrome due to CD40L deficiency", "Hyper-IgM Immunodeficiency Syndrome, Type 1", "Hyper IgM Immunodeficiency Syndrome, Type 1", "X-linked immunodeficiency with increased IgM", "immunodeficiency with increased IgM: X-linked", "Hyper-IgM syndrome due to CD40 ligand deficiency", "hyper-IgM syndrome due to CD40 ligand deficiency", "Immunodeficiency with Hyper-IgM, X-Linked, Type 1", "CD40 - Cluster of differentiation ligand deficiency", "X-linked hyper-immunoglobulin M syndrome (disorder)", "X-linked immunodeficiency with increased IgM (diagnosis)", "immunodeficiency, X-linked, with hyper-IgM, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyper-IgM syndrome type 1", "shortest_name_length": 4}
{"curie": "UMLS:C0264522", "names": ["Passive pneumonia", "Hypostatic pneumonia", "pneumonia hypostatic", "hypostatic pneumonia", "Pneumonia hypostatic", "pneumonia; hypostatic", "hypostatic; pneumonia", "Hypostatic pneumonia (disorder)", "hypostatic pneumonia (diagnosis)", "Hypostatic pneumonia, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypostatic pneumonia", "shortest_name_length": 17}
{"curie": "UMLS:C4743625", "names": ["Pituitary Gland Multiple Adenomas", "Multiple Synchronous PitNET/Adenomas of Distinct Lineages", "Multiple Synchronous Pituitary Neuroendocrine Tumors of Distinct Lineages", "Multiple Synchronous Pituitary Neuroendocrine Tumors/Adenomas of Distinct Lineages"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Multiple Synchronous Pituitary Neuroendocrine Tumors of Distinct Lineages", "shortest_name_length": 33}
{"curie": "UMLS:C1882916", "names": ["Rectal Small Cell Carcinoma", "Rectal Small Cell Neuroendocrine Cancer", "Rectal Small Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rectal Small Cell Neuroendocrine Carcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0014041", "names": ["AUTS19", "susceptibility to autism 19", "autism, susceptibility to, 19", "AUTISM, SUSCEPTIBILITY TO, 19", "autism, susceptibility to, type 19"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autism, susceptibility to, 19", "shortest_name_length": 6}
{"curie": "UMLS:C4683741", "names": ["Stage IB Mycosis Fungoides and Sezary Syndrome AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Mycosis Fungoides and Sezary Syndrome AJCC v8", "shortest_name_length": 54}
{"curie": "MONDO:0003752", "names": ["Frontal Sinus Papilloma", "frontal sinus Schneiderian papilloma", "Frontal Sinus Schneiderian Papilloma", "Schneiderian papilloma of frontal sinus", "Schneiderian Papilloma of Frontal Sinus", "Schneiderian papilloma of the Frontal sinus", "Schneiderian papilloma of the frontal sinus", "Schneiderian Papilloma of the Frontal Sinus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontal sinus Schneiderian papilloma", "shortest_name_length": 23}
{"curie": "UMLS:C5421351", "names": ["Unresectable Thyroid Gland Papillary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Thyroid Gland Papillary Carcinoma", "shortest_name_length": 46}
{"curie": "MONDO:0015221", "names": ["isolated respiratory or mediastinal malformation", "nonsyndromic respiratory or mediastinal malformation", "non-syndromic respiratory or mediastinal malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-syndromic respiratory or mediastinal malformation", "shortest_name_length": 48}
{"curie": "UMLS:C3275113", "names": ["Moderate Cardiac Valve Regurgitation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Moderate Cardiac Valve Regurgitation", "shortest_name_length": 36}
{"curie": "MONDO:0016596", "names": ["HPMR", "HPMRS", "Mabry disease", "Mabry syndrome", "Hyperphosphatasia with Mental Retardation", "Hyperphosphatasemia with mental retardation", "Hyperphosphatasaemia with mental retardation", "Hyperphosphatasemia with intellectual disability", "Hyperphosphatasaemia with intellectual disability", "hyperphosphatasia-intellectual disability syndrome", "Hyperphosphatasemia with intellectual disabilities", "hyperphosphatasia with mental retardation syndrome", "Hyperphosphatasia-intellectual disability syndrome", "Hyperphosphatasia with seizures and neurologic deficit", "hyperphosphatasia with intellectual disability syndrome", "Hyperphosphatasemia with intellectual disability (disorder)", "Hyperphosphatasemia with intellectual disabilities (diagnosis)", "hyperphosphatasia with impaired intellectual development syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperphosphatasia-intellectual disability syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0017803", "names": ["PPAOS", "primary progressive apraxia of speech"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary progressive apraxia of speech", "shortest_name_length": 5}
{"curie": "MONDO:0019334", "names": ["autosomal recessive hyperinsulinism due to Kir6.2 deficiency", "autosomal recessive hyperinsulinemic hypoglycemia due to Kir6.2 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive hyperinsulinism due to Kir6.2 deficiency", "shortest_name_length": 60}
{"curie": "UMLS:C0279597", "names": ["non-T, non-B, cALLa negative adult ALL", "non-B, non-T, cALLa negative adult ALL", "adult ALL, non-T, non-B, cALLa negative", "cALLa negative, non T, non B, adult ALL", "cALLa negative, non-T, non-B, adult ALL", "ALL, adult non-T, non-B, cALLa negative", "ALL, adult non T, non B, cALLa negative", "non T, non B, adult ALL, cALLa negative", "adult ALL, non T, non B, cALLa negative", "ALL, non-T, non-B, cALLa negative, adult", "ALL, cALLa negative, non-T, non-B, adult", "ALL, non T, non B, cALLa negative, adult", "leukemia, cALLa negative, non-T, non-B, adult", "leukemia, ALL non-T, non-B, cALLa negative, adult", "Non-T Non-B CALLA Negative Acute Lymphoblastic Leukemia", "Non-T Non-B CALLA Negative Adult Acute Lymphoblastic Leukemia", "non-T, non-B, cALLa negative adult acute lymphocytic leukemia", "non B, non T, cALLa negative adult acute lymphocytic leukemia", "non T, non B, cALLa negative adult acute lymphocytic leukemia", "leukemia, adult acute lymphocytic non-T, non-B, cALLa negative", "acute lymphocytic leukemia, adult non-T, non-B, cALLa negative", "non-T, non-B, cALLa negative adult acute lymphoblastic leukemia", "acute lymphoblastic leukemia, adult non-T, non-B, cALLa negative"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-T Non-B CALLA Negative Adult Acute Lymphoblastic Leukemia", "shortest_name_length": 38}
{"curie": "MONDO:0001178", "names": ["Pseudopterygium", "pseudopterygium", "Pseudopterygium (disorder)", "pseudopterygium (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudopterygium", "shortest_name_length": 15}
{"curie": "UMLS:C1883722", "names": ["Stage 0a Bladder Cancer", "Stage 0a Bladder Carcinoma", "Stage 0a Carcinoma of Bladder", "Stage 0a Carcinoma of the Bladder", "Stage 0a Bladder Urothelial Cancer", "Stage 0a Urinary Bladder Carcinoma", "Stage 0a Bladder Urothelial Carcinoma", "Stage 0a Carcinoma of Urinary Bladder", "Stage 0a Carcinoma of the Urinary Bladder", "Non-Invasive Papillary Urothelial Carcinoma", "Non-Invasive Papillary Carcinoma of Bladder", "Stage 0a Bladder Urothelial Carcinoma AJCC v6", "Stage 0a Bladder Urothelial Carcinoma AJCC v7", "Non-Invasive Papillary Carcinoma of the Bladder", "Non-Invasive Papillary Carcinoma of Urinary Bladder", "Stage 0a Bladder Urothelial Carcinoma AJCC v6 and v7", "Non-Invasive Papillary Carcinoma of the Urinary Bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0a Bladder Urothelial Carcinoma AJCC v6 and v7", "shortest_name_length": 23}
{"curie": "MONDO:0003736", "names": ["Ca phobia", "fear cancer", "cancer fear", "Cancerphobia", "cancerphobia", "Cancer phobia", "cancer phobia", "cancerophobia", "Cancerophobia", "Phobia;cancer", "Phobia, cancer", "Fear of cancer", "fear of cancer", "Fear (of);cancer", "Fear of getting cancer", "fear of getting cancer", "fear of getting cancer (finding)", "Fear of getting cancer (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cancerophobia", "shortest_name_length": 9}
{"curie": "UMLS:C1710140", "names": ["Sparsely Granulated Somatotroph PitNET/Adenoma", "Sparsely Granulated Pituitary Gland Somatotroph Adenoma", "Sparsely Granulated Somatotroph Pituitary Neuroendocrine Tumor", "Sparsely Granulated Somatotroph Pituitary Neuroendocrine Tumor/Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sparsely Granulated Somatotroph Pituitary Neuroendocrine Tumor", "shortest_name_length": 46}
{"curie": "MONDO:0100478", "names": ["BRMUTD", "BRAIN MALFORMATIONS AND URINARY TRACT DEFECTS", "brain malformations with or without urinary tract defects", "BRAIN MALFORMATIONS WITH OR WITHOUT URINARY TRACT DEFECTS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brain malformations with or without urinary tract defects", "shortest_name_length": 6}
{"curie": "UMLS:C4053505", "names": ["SBT/APST", "Borderline Ovarian Serous Tumor/Atypical Proliferative Ovarian Serous Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Ovarian Serous Tumor/Atypical Proliferative Ovarian Serous Tumor", "shortest_name_length": 8}
{"curie": "MONDO:0003058", "names": ["Microcystic Meningioma", "microcystic meningioma", "Microcystic meningioma", "Meningioma, Microcystic", "Microcystic Meningiomas", "Meningiomas, Microcystic", "Microcystic meningioma (morphologic abnormality)", "microcystic meningioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcystic meningioma", "shortest_name_length": 22}
{"curie": "UMLS:C0948978", "names": ["Catheter site cellulitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Catheter site cellulitis", "shortest_name_length": 24}
{"curie": "UMLS:C1266186", "names": ["Spontaneously Regressed Retinoblastoma", "Retinoblastoma, spontaneously regressed", "Spontaneously Regressing Retinoblastoma", "Retinoblastoma, spontaneously regressed (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retinoblastoma, spontaneously regressed", "shortest_name_length": 38}
{"curie": "MONDO:0003227", "names": ["Prosopagnosia", "prosopagnosia", "FACE BLINDNESS", "Face Blindness", "Prosopagnosias", "Facial agnosia", "face blindness", "Face blindness", "Agnosia for Face", "Agnosia for Faces", "Agnosia for faces", "prosopagnosia (disease)", "Prosopagnosia (finding)", "Facial Recognition Agnosia", "Agnosia, Facial Recognition", "Recognition Agnosia, Facial", "Facial Recognition Agnosias", "Recognition Agnosias, Facial", "Agnosias, Facial Recognition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prosopagnosia", "shortest_name_length": 13}
{"curie": "MONDO:0024529", "names": ["PMV", "MVP1", "MMVP1", "BARLOW SYNDROME", "barlow syndrome", "FLOPPY MITRAL VALVE", "floppy mitral valve", "click-murmur syndrome", "CLICK-MURMUR SYNDROME", "prolapsed mitral valve", "MITRAL VALVE PROLAPSE 1", "mitral valve prolapse 1", "mitral regurgitation, familial", "MITRAL REGURGITATION, FAMILIAL", "mitral valve prolapse, familial", "MYXOMATOUS MITRAL VALVE PROLAPSE 1", "Myxomatous Mitral Valve Prolapse 1", "myxomatous mitral valve prolapse 1", "mitral valve prolapse, myxomatous 1", "Mitral Valve Prolapse, Myxomatous 1", "MITRAL VALVE PROLAPSE, MYXOMATOUS 1", "myxomatous valvular disease, familial", "MYXOMATOUS VALVULAR DISEASE, FAMILIAL", "mitral valve prolapse, familial, X-linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MVP1", "shortest_name_length": 3}
{"curie": "MONDO:0003314", "names": ["vaginal endometrial stromal tumor", "Vaginal Endometrioid Stromal and Related Tumors", "vagina endometrioid stromal and related neoplasms", "Vaginal Endometrioid Stromal and Related Neoplasms", "endometrioid stromal and related neoplasms of vagina", "Endometrioid Stromal and Related Tumors of the Vagina", "endometrioid stromal and related tumors of the vagina", "Endometrioid Stromal and Related Neoplasms of the Vagina", "endometrioid stromal and related neoplasms of the vagina"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometrioid stromal and related neoplasms of the vagina", "shortest_name_length": 33}
{"curie": "MONDO:0021340", "names": ["intertrigo", "Intertrigo", "INTERTRIGO", "Eczema intertrigo", "Erythema intertrigo", "erythema; intertrigo", "intertrigo; erythema", "Intertrigo (disorder)", "intertrigo (diagnosis)", "intertriginous; eczema", "eczema; intertriginous", "Intertriginous dermatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intertrigo", "shortest_name_length": 10}
{"curie": "MONDO:0016031", "names": ["faces syndrome", "FACES syndrome", "Friedman-Goodman syndrome", "Friedman Goodman syndrome", "Facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome", "facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome", "facial features (unique), anorexia, cachexia, eye and skin anomalies", "Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome", "FACES (facial dysmorphism, anorexia, cachexia, eye and skin anomalies) syndrome", "Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0002163", "names": ["Thymolipoma", "thymus lipoma", "lipoma of thymus", "Thymolipomatous hamartoma", "Thymolipomatous Hamartoma", "Thymolipoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thymus lipoma", "shortest_name_length": 11}
{"curie": "UMLS:C0276680", "names": ["candida albicans infection", "Candida albicans infection", "albicans candida infections", "Infection by Candida albicans", "Infection caused by Candida albicans", "Infection caused by Candida albicans (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infection by Candida albicans", "shortest_name_length": 26}
{"curie": "UMLS:C1275210", "names": ["Sebaceoma", "Sebomatricoma", "Sebocrine adenoma", "Sebocrine Adenoma", "Sebaceoma (disorder)", "Infundibular Adenoma", "Infundibular adenoma", "Sebaceous Epithelioma", "Poroma-Like Adnexal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sebaceoma", "shortest_name_length": 9}
{"curie": "MONDO:0013699", "names": ["LYNCH4", "HNPCC4", "Lynch syndrome 4", "LYNCH SYNDROME 4", "PMS2 hereditary nonpolyposis colon cancer", "hereditary nonpolyposis colorectal cancer type 4", "colorectal cancer, hereditary nonpolyposis, type 4", "COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 4", "Colorectal Cancer, Hereditary Nonpolyposis, Type 4", "hereditary nonpolyposis colon cancer caused by mutation in PMS2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lynch syndrome 4", "shortest_name_length": 6}
{"curie": "UMLS:C0279644", "names": ["Pediatric AMML", "pediatric AMML", "childhood AMML", "Childhood AMML", "AMML, childhood", "Pediatric AMMoL", "pediatric AMMoL", "AMML, pediatric", "childhood AMMoL", "Childhood AMMoL", "AMMoL, childhood", "AMMoL, pediatric", "childhood AMML M4", "Childhood Acute M4 Leukemia", "Pediatric Acute M4 Leukemia", "childhood acute M4 leukemia", "pediatric acute M4 leukemia", "M4 leukemia, childhood acute", "Acute Myelomonocytic Leukemia", "pediatric acute myelomonocytic leukemia", "Pediatric Acute Myelomonocytic Leukemia", "childhood acute myelomonocytic leukemia", "Childhood Acute Myelomonocytic Leukemia", "acute myelomonocytic leukemia, childhood", "myelomonocytic leukemia, childhood acute", "leukemia, childhood acute myelomonocytic", "M4 pediatric acute myelomonocytic leukemia", "M4 Pediatric Acute Myelomonocytic Leukemia", "M4 Childhood Acute Myelomonocytic Leukemia", "acute myelomonoblastic leukemia, childhood", "myelomonoblastic leukemia, childhood acute", "M4 childhood acute myelomonocytic leukemia", "Childhood Acute Myelomonocytic Leukemia (M4)", "childhood acute myelomonocytic leukemia (M4)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Acute Myelomonocytic Leukemia", "shortest_name_length": 14}
{"curie": "MONDO:0008853", "names": ["Bss", "BSS", "BBRSAY", "Barber-Say Syndrome", "Barber Say syndrome", "BARBER-SAY SYNDROME", "BARBER-SAY syndrome", "Barber-Say syndrome", "Barber-Say syndrome (disorder)", "hypertrichosis atrophic skin ectropion macrostomia", "HYPERTRICHOSIS, ATROPHIC SKIN, ECTROPION, AND MACROSTOMIA", "Hypertrichosis, atrophic skin, ectropion, and macrostomia", "hypertrichosis, atrophic skin, ectropion, and macrostomia", "Hypertrichosis-atrophic skin-ectropion-macrostomia syndrome", "hypertrichosis-atrophic skin-ectropion-macrostomia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Barber-Say syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0100353", "names": ["HHV-7 infection", "HHV-7 infectious disease", "herpesvirus-7 infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HHV-7 infectious disease", "shortest_name_length": 15}
{"curie": "UMLS:C0677687", "names": ["Stage II Grade 1 Follicular Lymphoma", "Stage II Grade 1 Contiguous Follicular Lymphoma", "Contiguous Grade I Follicular Lymphoma Stage II", "Contiguous Stage II Grade I Follicular Lymphoma", "contiguous stage II grade 1 follicular lymphoma", "Ann Arbor Stage II Grade 1 Contiguous Follicular Lymphoma", "Contiguous Stage II Follicular Small Cleaved Cell Lymphoma", "Stage II Contiguous Follicular Small Cleaved Cell Lymphoma", "Contiguous Follicular Small Cleaved Cell Lymphoma Stage II", "Contiguous Grade I Follicular Small Cleaved Cell Lymphoma Stage II", "contiguous stage II grade I follicular small cleaved cell lymphoma", "Contiguous Stage II Grade I Follicular Small Cleaved Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage II Grade 1 Contiguous Follicular Lymphoma", "shortest_name_length": 36}
{"curie": "MONDO:0017229", "names": ["Del(12)(p13.33)", "distal monosomy 12p", "distal deletion 12p", "distal monosomy type 12p", "12p13.33 microdeletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal monosomy 12p", "shortest_name_length": 15}
{"curie": "MONDO:0033170", "names": ["statin toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "statin toxicity", "shortest_name_length": 15}
{"curie": "MONDO:0015104", "names": ["PCT", "pct", "Urocoproporphyria", "Symptomatic porphyria", "porphyria cutania tarda", "PORPHYRIA CUTANEA TARDA", "porphyria cutanea tarda", "Porphyria cutanea tarda", "Porphyria Cutanea Tarda", "Constitutional porphyria", "porphyria; cutanea tarda", "cutanea tarda; porphyria", "Cutaneous hepatic porphyria", "Porphyria cutanea tarda, NOS", "Porphyria cutanea tarda (PCT)", "PCT - Porphyria cutanea tarda", "porphyria cutanea tarda (PCT)", "PCT (porphyria cutanea tarda)", "porphyria; hepatocutaneous type", "Porphyria, hepatocutaneous type", "PORPHYRIA, HEPATOCUTANEOUS TYPE", "hepatocutaneous type; porphyria", "CHP - Cutaneous hepatic porphyria", "Porphyria cutanea tarda (disorder)", "porphyria cutanea tarda (diagnosis)", "PORPHYRIA CUTANEA TARDA SYMPTOMATICA", "Porphyria cutanea tarda symptomatica"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "porphyria cutanea tarda", "shortest_name_length": 3}
{"curie": "UMLS:C5239366", "names": ["Refractory Anaplastic Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Anaplastic Astrocytoma", "shortest_name_length": 33}
{"curie": "UMLS:C5556664", "names": ["HPV-Independent Cervical Adenocarcinoma In Situ", "Human Papillomavirus-Independent Cervical Adenocarcinoma In Situ"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Human Papillomavirus-Independent Cervical Adenocarcinoma In Situ", "shortest_name_length": 47}
{"curie": "MONDO:0014166", "names": ["PNH2", "PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 2", "paroxysmal nocturnal hemoglobinuria 2", "PIGT paroxysmal nocturnal hemoglobinuria", "paroxysmal nocturnal hemoglobinuria type 2", "paroxysmal nocturnal hemoglobinuria caused by mutation in PIGT", "paroxysmal nocturnal hemoglobinuria 2, autosomal dominant, somatic mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paroxysmal nocturnal hemoglobinuria 2", "shortest_name_length": 4}
{"curie": "MONDO:0005875", "names": ["pseudo-fowlpest", "Newcastle fever", "Pseudo-fowlpest", "Newcastle disease", "Newcastle Disease", "NEWCASTLE DISEASE", "newcastle disease", "Disease, Newcastle", "Newcastle's disease", "Newcastle (etiology)", "Avian pneumoencephalitis", "Newcastle (manifestation)", "Newcastle disease (disorder)", "Newcastle disease (diagnosis)", "disease (or disorder); Newcastle (etiology)", "disease (or disorder); Newcastle (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Newcastle disease", "shortest_name_length": 15}
{"curie": "MONDO:0005616", "names": ["lung mucoepidermoid cancer", "Lung Mucoepidermoid Cancer", "lung mucoepidermoid carcinoma", "Lung Mucoepidermoid Carcinoma", "Mucoepidermoid carcinoma of lung", "mucoepidermoid carcinoma of lung", "pulmonary mucoepidermoid carcinoma", "mucoepidermoid carcinoma of the lung", "Mucoepidermoid carcinoma of lung (disorder)", "mucoepidermoid carcinoma of lung (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary mucoepidermoid carcinoma", "shortest_name_length": 26}
{"curie": "UMLS:C1709584", "names": ["Polyhormonal Adenoma", "Multihormonal Adenoma", "Plurihormonal Adenoma", "Plurihormonal PitNET/Adenoma", "Unusual Plurihormonal Tumor/Adenoma", "Multihormonal Pituitary Gland Adenoma", "Plurihormonal Pituitary Neuroendocrine Tumor", "Plurihormonal Pituitary Neuroendocrine Tumor/Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Plurihormonal Pituitary Neuroendocrine Tumor", "shortest_name_length": 20}
{"curie": "MONDO:0100204", "names": ["human rubulavirus 2 infectious disease", "infection due to human parainfluenza virus 2", "parainfluenza virus type 2 infectious disease", "infection caused by human parainfluenza virus 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parainfluenza virus type 2 infectious disease", "shortest_name_length": 38}
{"curie": "MONDO:0018473", "names": ["LDLCQ5", "HLP type 3", "remnant disease", "Broad beta disease", "BROAD BETA DISEASE", "broad beta disease", "Type III lipidemia", "Broad-beta disease", "Broad Beta Disease", "dyslipidemia type 3", "Type III lipidaemia", "hyperlipidemia type 3", "floating beta disease", "Floating beta disease", "Hyperlipidemia type 3", "Dysbetalipoproteinemia", "Remnant Hyperlipidemia", "DYSBETALIPOPROTEINEMIA", "dysbetalipoproteinemia", "remnant hyperlipidemia", "Remnant hyperlipidemia", "Dysbetalipoproteinaemia", "remnant removal disease", "hyperlipidemia type iii", "Type III hyperlipidemia", "Remnant hyperlipidaemia", "type iii hyperlipidemia", "HYPERLIPIDEMIA TYPE III", "Type III hyperlipidaemia", "Broad-Betalipoproteinemia", "BROAD-BETALIPOPROTEINEMIA", "Broad-betalipoproteinemia", "Apolipoprotein E deficiency", "hyperlipoproteinemia type 3", "Hyperlipoproteinemia type 3", "Familial dyslipidemia type 3", "Floating-Betalipoproteinemia", "Remnant hyperlipoproteinemia", "floating-betalipoproteinemia", "FLOATING-BETALIPOPROTEINEMIA", "HYPERLIPOPROTEINEMIA TYPE III", "Hyperlipoproteinemia Type III", "hyperlipoproteinemia type III", "hyperlipoproteinemia type iii", "Type III hyperlipoproteinemia", "type iii hyperlipoproteinemia", "Type III Hyperlipoproteinemia", "Remnant hyperlipoproteinaemia", "floating-beta; lipoproteinemia", "Type III hyperlipoproteinaemia", "Primary dysbetalipoproteinemia", "HYPERLIPOPROTEINEMIA, TYPE III", "hyperlipoproteinemia, type III", "lipoproteinemia; floating-beta", "Type III Hyperlipoproteinemias", "Hyperlipoproteinemia, Type III", "Broad-beta Hyperlipoproteinemia", "familial dysbetalipoproteinemia", "Primary dysbetalipoproteinaemia", "Hyperlipoproteinemias, Type III", "Familial Dysbetalipoproteinemia", "Familial dysbetalipoproteinemia", "Hyperlipoproteinemia, Broad-beta", "Hyperlipoproteinemia, Broad beta", "Dysbetalipoproteinemia, Familial", "Familial dysbetalipoproteinaemia", "carbohydrate induced hyperlipemia", "Carbohydrate induced hyperlipemia", "carbohydrate hyperlipemia induced", "Carbohydrate induced hyperlipaemia", "Fredrickson type III hyperlipidemia", "familial type 3 hyperlipoproteinemia", "familial hyperlipoproteinemia type 3", "Familial type 3 hyperlipoproteinemia", "Familial type 3 hyperlipoproteinaemia", "familial hyperlipoproteinemia type III", "Familial type III hyperlipoproteinemia", "Familial type III hyperlipoproteinaemia", "Fredrickson type III hyperlipoproteinemia", "APOLIPOPROTEIN E, DEFICIENCY OR DEFECT OF", "apolipoprotein E, deficiency or defect of", "Apolipoprotein E, Deficiency or Defect of", "hyperlipoproteinemia type III (diagnosis)", "hyperlipoproteinemia; Fredrickson type III", "Fredrickson; type III hyperlipoproteinemia", "Fredrickson type III hyperlipoproteinaemia", "Hyperlipoproteinemia, Frederickson type III", "familial dysbetalipoproteinemia (diagnosis)", "Familial Hyperbeta- and Prebetalipoproteinemia", "familial Hyperbeta- and Prebetalipoproteinemia", "FAMILIAL HYPERBETA- AND PREBETALIPOPROTEINEMIA", "Familial type 3 hyperlipoproteinemia (disorder)", "Fredrickson type III hyperlipidemia (diagnosis)", "FAMILIAL HYPERCHOLESTEROLEMIA WITH HYPERLIPEMIA", "Familial Hypercholesterolemia with Hyperlipemia", "familial hypercholesterolemia with hyperlipemia", "Familial hypercholesterolemia with hyperlipemia", "Familial hypercholesterolaemia with hyperlipaemia", "familial hypercholesterolaemia with hyperlipaemia", "CORONARY ARTERY DISEASE, SEVERE, SUSCEPTIBILITY TO", "coronary artery disease, Severe, Susceptibility to", "Dysbetalipoproteinemia due to Defect in Apolipoprotein E-d", "DYSBETALIPOPROTEINEMIA DUE TO DEFECT IN APOLIPOPROTEIN E-d", "dysbetalipoproteinemia due to defect in apolipoprotein E-D", "HYPERLIPEMIA WITH FAMILIAL HYPERCHOLESTEROLEMIC XANTHOMATOSIS", "hyperlipemia with Familial Hypercholesterolemic xanthomatosis", "Hyperlipemia with Familial Hypercholesterolemic Xanthomatosis", "Familial hyperbetalipoproteinemia and hyperprebetalipoproteinemia", "Familial hyperbetalipoproteinaemia and hyperprebetalipoproteinaemia", "LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 5", "low density lipoprotein cholesterol level quantitative trait locus 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperlipoproteinemia type 3", "shortest_name_length": 6}
{"curie": "UMLS:C5557167", "names": ["Stage IIA Cervical Cancer AJCC v9", "Stage IIA Cervical Carcinoma AJCC v9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Cervical Cancer AJCC v9", "shortest_name_length": 33}
{"curie": "UMLS:C0266323", "names": ["Congenital Hydroureter", "Congenital hydroureter", "congenital; hydroureter", "hydroureter; congenital", "Hydroureter - congenital", "congenital anomaly hydroureter", "Congenital hydroureter (disorder)", "Congenital hydroureter (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital hydroureter", "shortest_name_length": 22}
{"curie": "MONDO:0001651", "names": ["scrotum squamous cell carcinoma", "Scrotal Squamous Cell Carcinoma", "scrotal squamous cell carcinoma", "Scrotal squamous cell carcinoma", "squamous cell carcinoma of scrotum", "Squamous cell carcinoma of scrotum", "Squamous Cell Carcinoma of Scrotum", "Squamous Cell Carcinoma of the Scrotum", "squamous cell carcinoma of the scrotum", "Squamous cell carcinoma of scrotum (disorder)", "squamous cell carcinoma of scrotum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scrotum squamous cell carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0017393", "names": ["BMRS", "SBBYS syndrome", "Young Simpson syndrome", "blepharophimosis syndrome Ohdo type", "Say Barber Biesecker Young-Simpson syndrome", "blepharophimosis mental retardation syndromes", "blepharophimosis intellectual disability syndromes", "blepharophimosis - intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blepharophimosis - intellectual disability syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0020567", "names": ["AOP", "apnea prematurity", "apnea of prematurity", "Apnea of prematurity", "Apnea of Prematurity", "Apnoea of prematurity", "apnoea of prematurity", "Apnea of prematurity (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "apnea of prematurity", "shortest_name_length": 3}
{"curie": "UMLS:C1260871", "names": ["Acetonemia", "ACETONEMIA", "acetonemia", "Acetonaemia", "ACETONAEMIA", "Acetonemia (disorder)", "acetonemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acetonemia", "shortest_name_length": 10}
{"curie": "UMLS:C0346345", "names": ["Lacrimal Gland Benign Mixed Tumor", "Lacrimal Gland Pleomorphic Adenoma", "Pleomorphic adenoma lacrimal gland", "Benign Mixed Tumor of Lacrimal Gland", "Pleomorphic adenoma of lacrimal gland", "Pleomorphic Adenoma of Lacrimal Gland", "Benign Mixed Tumor of the Lacrimal Gland", "Pleomorphic Adenoma of the Lacrimal Gland", "Pleomorphic adenoma of lacrimal gland (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pleomorphic adenoma of lacrimal gland", "shortest_name_length": 33}
{"curie": "MONDO:0021489", "names": ["hidradenoma", "Benign sweat gland tumor", "benign sweat gland tumor", "Benign Sweat Gland Tumor", "Benign sweat gland tumour", "Sweat gland tumor, benign", "Sweat gland tumour, benign", "sweat gland benign neoplasm", "benign tumor of sweat gland", "Benign Tumor of Sweat Gland", "Benign Sweat Gland Neoplasm", "benign sweat gland neoplasm", "sweat gland neoplasm, benign", "Sweat Gland Neoplasm, Benign", "Benign Neoplasm of Sweat Gland", "Benign neoplasm of sweat gland", "benign neoplasm of sweat gland", "benign tumor of the sweat gland", "Benign Tumor of the Sweat Gland", "benign neoplasm of sweat glands", "Benign Neoplasm of the Sweat Gland", "benign neoplasm of the sweat gland", "Benign neoplasm of sweat gland (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of sweat gland", "shortest_name_length": 11}
{"curie": "MONDO:0020776", "names": ["chlamydiaceae infection", "Chlamydiaceae Infection", "Infection, Chlamydiaceae", "chlamydiaceae infections", "Chlamydiaceae Infections", "Infections, Chlamydiaceae"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chlamydiaceae infections", "shortest_name_length": 23}
{"curie": "MONDO:0014998", "names": ["GLC3E", "glaucoma 3, primary congenital, E", "GLAUCOMA 3, PRIMARY CONGENITAL, E", "glaucoma 3, primary congenital, type E", "glaucoma 3, primary congenital, E; GLC3E"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glaucoma 3, primary congenital, E", "shortest_name_length": 5}
{"curie": "UMLS:C2955673", "names": ["urate nephropathy", "Urate nephropathy", "uric acid nephropathy", "Uric acid nephropathy", "URIC ACID NEPHROPATHY", "Urate nephropathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urate nephropathy", "shortest_name_length": 17}
{"curie": "MONDO:0002403", "names": ["synovium cancer", "Malignant Synovial Tumor", "malignant synovial tumor", "malignant tumor of synovium", "Malignant Tumor of Synovium", "Malignant Synovial Neoplasm", "malignant synovial neoplasm", "malignant tumor of Synovium", "malignant neoplasm of synovium", "Malignant Neoplasm of Synovium", "malignant tumor of the synovium", "layer of synovial tissue cancer", "Malignant Tumor of the Synovium", "cancer of layer of synovial tissue", "malignant neoplasm of the synovium", "Malignant Neoplasm of the Synovium", "synovial membrane of synovial joint cancer", "malignant layer of synovial tissue neoplasm", "cancer of synovial membrane of synovial joint", "malignant neoplasm of layer of synovial tissue", "malignant synovial membrane of synovial joint neoplasm", "malignant neoplasm of synovial membrane of synovial joint"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "synovium cancer", "shortest_name_length": 15}
{"curie": "MONDO:0001004", "names": ["Schistosis", "Slate-workers' lung", "Slate pneumoconiosis", "Slate Pneumoconiosis", "slate pneumoconiosis", "Schistosis (disorder)", "Schistosis (diagnosis)", "Slate workers pneumoconiosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "slate pneumoconiosis", "shortest_name_length": 10}
{"curie": "UMLS:C5419188", "names": ["Advanced Chromophobe Renal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Chromophobe Renal Cell Carcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0024561", "names": ["VMD3", "vitelliform macular dystrophy 3", "macular dystrophy, vitelliform, 3", "PRPH2 vitelliform macular dystrophy", "foveomacular dystrophy, adult-onset", "vitelliform macular dystrophy, adult-onset", "vitelliform macular dystrophy caused by mutation in PRPH2", "foveomacular dystrophy, adult-onset, with or without choroidal neovascularization"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitelliform macular dystrophy 3", "shortest_name_length": 4}
{"curie": "UMLS:C4764207", "names": ["Refractory Endometrial Mixed Cell Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Endometrial Mixed Cell Adenocarcinoma", "shortest_name_length": 48}
{"curie": "UMLS:C2826330", "names": ["RARS-T", "MDS/MPN-RS-T", "Essential Thrombocythemia with Ring Sideroblasts", "MDS/MPN with Ring Sideroblasts and Thrombocytosis", "Refractory anemia with ring sideroblasts associated with marked thrombocytosis", "Refractory Anemia with Ring Sideroblasts Associated with Marked Thrombocytosis", "refractory anemia with ring sideroblasts associated with marked thrombocytosis", "Myelodysplastic/Myeloproliferative Neoplasm with Ring Sideroblasts and Thrombocytosis", "refractory anemia with ring sideroblasts associated with marked thrombocytosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myelodysplastic/Myeloproliferative Neoplasm with Ring Sideroblasts and Thrombocytosis", "shortest_name_length": 6}
{"curie": "UMLS:C0392534", "names": ["ECTOPIC PREGNANCY RUPTURE", "Aborted ectopic pregnancy", "RUPTURED ECTOPIC PREGNANCY", "ruptured ectopic pregnancy", "ectopic pregnancy ruptured", "Ruptured ectopic pregnancy", "pregnancy; ectopic (ruptured)", "Ruptured ectopic pregnancy (disorder)", "ruptured ectopic pregnancy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ruptured ectopic pregnancy", "shortest_name_length": 25}
{"curie": "MONDO:0009318", "names": ["HSS", "birdlike facies", "Hallerman-Streiff", "Hallermann syndrome", "Hallermann Syndrome", "Francois dyscephalia", "Hallermanns Syndrome", "Hallermann's Syndrome", "Hallermann's syndrome", "hallermann's syndrome", "Syndrome, Hallermann's", "oculomandibulodyscephaly", "mandibulofacial dysmorphia", "hallerman streiff syndrome", "hallerman-streiff syndrome", "Hallerman-Streiff syndrome", "oculomandibular dyscephaly", "Hallermann Streiff syndrome", "Hallermann Streiff Syndrome", "Hallermann-Streiff syndrome", "HALLERMANN-STREIFF SYNDROME", "hallermann streiff syndrome", "hallermann-streiff syndrome", "Hallermann-Streiff Syndrome", "Hallerman - Streiff syndrome", "Syndrome, Hallermann-Streiff", "oculomandibulofacial syndrome", "Francois Dyscephalic Syndrome", "Oculomandibulofacial syndrome", "FRANCOIS DYSCEPHALIC SYNDROME", "François dyscephalic syndrome", "Francois dyscephalic syndrome", "Syndrome, Francois Dyscephalic", "Dyscephalic Syndrome, Francois", "oculomandibulodyscephaly (OMD)", "FranC'ois dyscephalic syndrome", "Francois Dyscephalic Syndromes", "Syndromes, Francois Dyscephalic", "Dyscephalic Syndromes, Francois", "mandibulo-oculofacial dyscephaly", "Hallermann-Streiff syndrome (HSS)", "mandibulo-oculofacial dysmorphism", "dyscephalia mandibulo-oculofacialis", "Ullrich and Fremerey-Dohna syndrome", "Hallermann-Streiff-Francois syndrome", "Hallermann Streiff Francois Syndrome", "Hallermann Streiff Francois syndrome", "Hallerman-Streiff syndrome (diagnosis)", "Hallermann-Streiff syndrome (disorder)", "oculomandibulodyscephaly-hypotrichosis syndrome", "Oculomandibulodyscephaly with hypotrichosis syndrome", "dyscephaly-congenital cataract-hypotrichosis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hallermann-Streiff syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C0268105", "names": ["Uricaciduria", "URICACIDURIA", "Hyperuricuria", "Uricaciduria, NOS", "Hyperuricuria, NOS", "Hyperuricuria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyperuricuria", "shortest_name_length": 12}
{"curie": "MONDO:0016855", "names": ["Mowat-Wilson syndrome due to del(2)q(22)", "Mowat-Wilson syndrome due to monosomy 2q22", "Mowat-Wilson syndrome due to 2q22 microdeletion", "Mowat-Wilson syndrome due to monosomy type 2q22", "Hirschsprung disease and intellectual disability due to del(2)(q22)", "Hirschsprung disease and intellectual disability due to monosomy 2q22", "Hirschsprung disease and intellectual disability due to 2q22 microdeletion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mowat-Wilson syndrome due to monosomy 2q22", "shortest_name_length": 40}
{"curie": "MONDO:0007570", "names": ["Lane disease", "lane disease", "Lane's disease", "Red palms disease", "erythema palmare hereditarium", "Erythema Palmare Hereditarium", "Erythema palmare hereditarium", "ERYTHEMA PALMARE HEREDITARIUM", "Erythema palmare hereditarium (disorder)", "Erythema palmare hereditarium (diagnosis)", "disorder of integument hereditary erythema palmare"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythema palmare hereditarium", "shortest_name_length": 12}
{"curie": "UMLS:C3898709", "names": ["Enteric-Type Sinonasal Adenocarcinoma", "Intestinal-Type Sinonasal Adenocarcinoma", "Sinonasal Adenocarcinoma, Intestinal-Type", "Nasal Cavity and Paranasal Sinus Adenocarcinoma, Intestinal-Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Adenocarcinoma, Intestinal-Type", "shortest_name_length": 37}
{"curie": "MONDO:0006116", "names": ["Breast Carcinoma by Gene Expression Profile", "breast carcinoma by gene expression profile"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast carcinoma by gene expression profile", "shortest_name_length": 43}
{"curie": "MONDO:0006380", "names": ["pleura sarcomatoid mesothelioma", "Pleural Sarcomatoid Mesothelioma", "pleural sarcomatoid mesothelioma", "sarcomatoid mesothelioma of pleura"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pleural sarcomatoid mesothelioma", "shortest_name_length": 31}
{"curie": "MONDO:0017082", "names": ["basal encephalocele", "Basal encephalocele", "Basal encephalocoele", "Basal encephalocele (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "basal encephalocele", "shortest_name_length": 19}
{"curie": "MONDO:0008482", "names": ["HIGH SCAPULA", "High scapula", "high scapula", "Sprengel anomaly", "sprengel deformity", "SPRENGEL DEFORMITY", "Sprengel deformity", "Sprengel's shoulder", "High shoulder blade", "deformity; Sprengel", "Sprengel; deformity", "deformity sprengels", "Sprengel's deformity", "sprengel's deformity", "Undescended shoulder", "deformities sprengels", "congenital elevation scapula", "Sprengel deformity (disease)", "Maladie de Sprengel familiale", "Congenital elevation of scapula", "congenital elevation of the scapula", "Congenital elevation of scapula (disorder)", "congenital upward displacement of the scapula", "Congenital, upward displacement of the scapula"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sprengel deformity", "shortest_name_length": 12}
{"curie": "UMLS:C4764341", "names": ["AIN2", "Anal Intraepithelial Neoplasia 2", "Anal Squamous Intraepithelial Neoplasia 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anal Intraepithelial Neoplasia 2", "shortest_name_length": 4}
{"curie": "MONDO:0010798", "names": ["RENAL TUBULOPATHY, DIABETES MELLITUS, AND CEREBELLAR ATAXIA", "renal tubulopathy, diabetes mellitus, and cerebellar ataxia", "proximal tubulopathy, diabetes mellitus and cerebellar ataxia", "proximal tubulopathy-diabetes mellitus-cerebellar ataxia syndrome", "Renal Tubulopathy, Diabetes Mellitus, and Cerebellar Ataxia due to Duplication of Mitochondrial DNA", "renal tubulopathy, diabetes mellitus, and cerebellar ataxia due to duplication of mitochondrial DNA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "proximal tubulopathy-diabetes mellitus-cerebellar ataxia syndrome", "shortest_name_length": 59}
{"curie": "MONDO:0005495", "names": ["Adrenal Disease", "Adrenal disease", "adrenal disease", "adrenal diseases", "Adrenal disorder", "ADRENAL DISORDER", "adrenal disorder", "adrenal disorders", "adrenal disordered", "ADRENAL DISEASE, NOS", "Adrenal disorder NOS", "adrenal gland disease", "Adrenal gland disease", "Adrenal Gland Disease", "Adrenal abnormalities", "adrenal disease gland", "adrenal disease glands", "DISORDER ADRENAL (NOS)", "adrenal diseases gland", "adrenal gland diseases", "adrenal disorder gland", "Adrenal Gland Disorder", "Gland Disease, Adrenal", "Disease, Adrenal Gland", "Adrenal Gland Diseases", "adrenal gland disorder", "Diseases, Adrenal Gland", "diseases adrenal glands", "Adrenal gland disorders", "Adrenal Gland Disorders", "adrenal disorders gland", "Gland Diseases, Adrenal", "adrenal gland disorders", "Adrenal glands--Diseases", "adrenal glands disorders", "Disease of adrenal gland", "disease of adrenal gland", "Diseases of Adrenal Gland", "disorder of adrenal gland", "Disorder of adrenal gland", "Disorders of adrenal glands", "disorders of adrenal glands", "Disease of adrenal gland, NOS", "adrenal disorders (diagnosis)", "DISEASES OF THE ADRENAL GLANDS", "Disorder of adrenal gland, NOS", "adrenal gland disease or disorder", "Abnormality of the adrenal glands", "Disorder of adrenal gland (disorder)", "disease or disorder of adrenal gland", "Disorder of adrenal gland, unspecified", "Unspecified disorder of adrenal glands"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adrenal gland disorder", "shortest_name_length": 15}
{"curie": "MONDO:0019875", "names": ["Beckwith-Wiedemann syndrome due to 11p15 microduplication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Beckwith-Wiedemann syndrome due to 11p15 microduplication", "shortest_name_length": 57}
{"curie": "MONDO:0015392", "names": ["glioma nasal", "Nasal Glioma", "nasal glioma", "Nasal glioma", "Glial Choristoma", "Ectopic Glial Tissue", "Neuroglial Heterotopia", "Nasal Glial Heterotopia", "Nasal glial heterotopia", "nasal glial heterotopia", "Nasal glial heterotopia (disorder)", "nasal glial heterotopia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasal glial heterotopia", "shortest_name_length": 12}
{"curie": "MONDO:0033641", "names": ["CPPRDD", "CLEFT PALATE, PROLIFERATIVE RETINOPATHY, AND DEVELOPMENTAL DELAY", "cleft palate, proliferative retinopathy, and developmental delay"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleft palate, proliferative retinopathy, and developmental delay", "shortest_name_length": 6}
{"curie": "MONDO:0001390", "names": ["transient refractive change", "Transient refractive change", "Transient refractive change (disorder)", "transient refractive change (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transient refractive change", "shortest_name_length": 27}
{"curie": "MONDO:0014991", "names": ["SCKL10", "SECKEL SYNDROME 10", "Seckel syndrome 10", "NSMCE2 Seckel syndrome", "Seckel syndrome type 10", "Seckel syndrome caused by mutation in NSMCE2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Seckel syndrome 10", "shortest_name_length": 6}
{"curie": "MONDO:0002759", "names": ["Bladder Verrucous Carcinoma", "bladder verrucous carcinoma", "verrucous carcinoma of bladder", "urinary bladder verrucous carcinoma", "bladder verrucous squamous cell carcinoma", "Bladder Verrucous Squamous Cell Carcinoma", "verrucous carcinoma of bladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder verrucous carcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0004209", "names": ["cerebral PNET", "Cerebral PNET", "PNET of cerebrum", "PNET of Cerebrum", "PNET of the cerebrum", "PNET of the Cerebrum", "cerebral hemisphere PNET", "Cerebral Hemisphere PNET", "PNET of Cerebral Hemispheres", "PNET of cerebral hemispheres", "Cerebral Embryonal Tumor, NOS", "PNET of the cerebral hemispheres", "PNET of the Cerebral Hemispheres", "cerebral primitive neuroectodermal tumor", "Cerebral Primitive Neuroectodermal Tumor", "primitive neuroectodermal tumor of cerebrum", "Primitive Neuroectodermal Tumor of Cerebrum", "Cerebral Primitive Neuroectodermal Neoplasm", "cerebral primitive neuroectodermal neoplasm", "Primitive Neuroectodermal Neoplasm of Cerebrum", "primitive neuroectodermal neoplasm of cerebrum", "Primitive Neuroectodermal Tumor of the Cerebrum", "primitive neuroectodermal tumor of the cerebrum", "Cerebral Embryonal Tumor, Not Otherwise Specified", "primitive neuroectodermal neoplasm of the cerebrum", "Primitive Neuroectodermal Neoplasm of the Cerebrum", "Cerebral Hemisphere Primitive Neuroectodermal Tumor", "cerebral hemisphere primitive neuroectodermal tumor", "cerebral hemisphere primitive neuroectodermal neoplasm", "Cerebral Hemisphere Primitive Neuroectodermal Neoplasm", "primitive neuroectodermal tumor of cerebral hemispheres", "Primitive Neuroectodermal Tumor of Cerebral Hemispheres", "primitive neuroectodermal neoplasm of cerebral hemispheres", "Primitive Neuroectodermal Neoplasm of Cerebral Hemispheres", "Primitive Neuroectodermal Tumor of the Cerebral Hemispheres", "primitive neuroectodermal tumor of the cerebral hemispheres", "primitive neuroectodermal neoplasm of the cerebral hemispheres", "Primitive Neuroectodermal Neoplasm of the Cerebral Hemispheres"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral primitive neuroectodermal tumor", "shortest_name_length": 13}
{"curie": "MONDO:0014767", "names": ["SCKL9", "Seckel syndrome 9", "SECKEL SYNDROME 9", "TRAIP Seckel syndrome", "Seckel syndrome type 9", "Seckel syndrome caused by mutation in TRAIP"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Seckel syndrome 9", "shortest_name_length": 5}
{"curie": "MONDO:0017288", "names": ["PPBFTDS", "DICER1 Syndrome", "dicer1 syndrome", "DICER1 syndrome", "DICER1-related pleuropulmonary blastoma", "PPB familial tumor susceptibility syndrome", "Pleuro-pulmonary blastoma familial tumor susceptibility", "Pleuropulmonary blastoma family tumor susceptibility syndrome", "Pleuropulmonary blastoma family tumour susceptibility syndrome", "Pleuropulmonary blastoma familial tumor and dysplasia syndrome", "Pleuropulmonary blastoma familial tumour and dysplasia syndrome", "pleuropulmonary blastoma familial tumor susceptibility syndrome", "Pleuropulmonary blastoma familial tumor susceptibility syndrome", "pleuro-pulmonary blastoma familial tumor susceptibility syndrome", "Pleuro-pulmonary blastoma familial tumor susceptibility syndrome", "DICER1-related pleuropulmonary blastoma cancer predisposition syndrome", "Pleuropulmonary blastoma family tumor susceptibility syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DICER1 syndrome", "shortest_name_length": 7}
{"curie": "MONDO:0013065", "names": ["POF7", "Pof7", "premature ovarian failure 7", "Premature Ovarian Failure 7", "PREMATURE OVARIAN FAILURE 7", "adrenocortical insufficiency", "NR5A1 primary ovarian failure", "primary ovarian insufficiency 7", "premature ovarian failure type 7", "ADRENAL INSUFFICIENCY, NR5A1-RELATED", "adrenal insufficiency, Nr5A1-related", "primary ovarian failure caused by mutation in NR5A1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "premature ovarian failure 7", "shortest_name_length": 4}
{"curie": "OMIM:104250", "names": ["RHR", "FNSS2", "RESTING HEART RATE", "Resting heart rate", "Heart rate^resting", "RESTING HEART RATE, VARIATION IN", "SHORT SLEEP, FAMILIAL NATURAL, 2", "Resting heart rate (observable entity)", "CONGESTIVE HEART FAILURE AND BETA-BLOCKER RESPONSE, MODIFIER OF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 3}
{"curie": "UMLS:C2987266", "names": ["Esophageal Rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Rhabdomyosarcoma", "shortest_name_length": 27}
{"curie": "MONDO:0002916", "names": ["brainstem intraparenchymal clear cell meningioma", "Brainstem Intraparenchymal Clear Cell Meningioma", "brain stem intraparenchymal clear cell meningioma", "Brain Stem Intraparenchymal Clear Cell Meningioma", "intraparenchymal clear cell meningioma of brainstem", "Intraparenchymal Clear Cell Meningioma of Brainstem", "Intraparenchymal Clear cell meningioma of the Brainstem", "intraparenchymal clear cell meningioma of the brainstem", "Intraparenchymal Clear Cell Meningioma of the Brainstem"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brainstem intraparenchymal clear cell meningioma", "shortest_name_length": 48}
{"curie": "UMLS:C4520974", "names": ["stage IV nasopharynx cancer", "Stage IV Nasopharyngeal Throat Cancer", "Stage IV Nasopharynx Carcinoma AJCC v6", "Stage IV Nasopharyngeal Cancer AJCC v6", "Nasopharyngeal Cancer, Stage IV AJCC v6", "Stage IV Nasopharyngeal Carcinoma AJCC v6", "Stage IV Carcinoma of Nasopharynx AJCC v6", "Stage IV Carcinoma of the Nasopharynx AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Nasopharyngeal Carcinoma AJCC v6", "shortest_name_length": 27}
{"curie": "MONDO:0019902", "names": ["Del(13)(q34)", "monosomy 13q34", "Monosomy 13q34", "monosomy type 13q34", "distal deletion 13q34", "Distal deletion 13q34", "Monosomy 13q34 syndrome", "Monosomy 13q34 (diagnosis)", "subtelomeric deletion 13q34", "Subtelomeric deletion 13q34", "Monosomy 13q34 syndrome (disorder)", "deletion of part of chromosome 13 monosomy 13q34"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "monosomy 13q34", "shortest_name_length": 12}
{"curie": "MONDO:0009897", "names": ["APBD", "APBN", "Adult Polyglucosan Body Disease", "adult polyglucosan body disease", "Adult polyglucosan body disease", "polyglucosan body disease, adult", "Polyglucosan body disease adult form", "polyglucosan body disease, adult form", "POLYGLUCOSAN BODY DISEASE, ADULT FORM", "Polyglucosan Body Disease, Adult Form", "POLYGLUCOSAN BODY NEUROPATHY, ADULT FORM", "polyglucosan body neuropathy, adult form", "Adult polyglucosan body disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult polyglucosan body disease", "shortest_name_length": 4}
{"curie": "UMLS:C0853026", "names": ["Porphyria non-acute"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Porphyria non-acute", "shortest_name_length": 19}
{"curie": "MONDO:0000569", "names": ["autoimmune endocrine disease", "Autoimmune endocrine disease", "Autoimmune endocrine disorder", "autoimmune endocrine disorder", "Endocrine autoimmune disorders", "endocrine system autoimmune disease", "autoimmune disease of endocrine system", "Autoimmune endocrine disease (disorder)", "autoimmune disorder of endocrine system", "autoimmune endocrine disease (diagnosis)", "endocrine system hypersensitivity reaction type II disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune disorder of endocrine system", "shortest_name_length": 28}
{"curie": "UMLS:C5447509", "names": ["Metastatic Visceral Disease", "Symptomatic Visceral Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Visceral Disease", "shortest_name_length": 27}
{"curie": "MONDO:0011136", "names": ["QPD", "BDPLT5", "FACTOR V QUEBEC", "Factor V Quebec", "factor 5 Quebec", "factor V Quebec", "Quebec platelet disorder", "QUEBEC PLATELET DISORDER", "platelet-type bleeding disorder 5", "BLEEDING DISORDER, PLATELET-TYPE, 5", "bleeding disorder, platelet-type, 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Quebec platelet disorder", "shortest_name_length": 3}
{"curie": "MONDO:0002898", "names": ["cancer skin", "skin cancer", "Skin Cancer", "SKIN CANCER", "Skin cancer", "skin cancers", "cancers skin", "Cancer, Skin", "Skin cancers", "Skin--Cancer", "Skin Cancers", "Cancers, Skin", "Cancer of Skin", "cancer of skin", "Cancer of skin", "of skin cancer", "Skin cancer, NOS", "CA - skin cancer", "CA - Skin cancer", "cancer of the skin", "Cancer of the Skin", "of the skin cancer", "zone of skin cancer", "Neoplasm malig;skin", "malignant skin tumor", "Malignant Skin Tumor", "cancer of zone of skin", "malignant skin neoplasm", "SKIN NEOPLASM MALIGNANT", "Malignant Tumor of Skin", "skin cancer (diagnosis)", "malignant neoplasm skin", "malignant tumor of skin", "Malignant tumor of skin", "Skin neoplasm malignant", "Malignant Skin Neoplasm", "skin neoplasm, malignant", "Malignant tumour of skin", "Skin Neoplasm, Malignant", "Malignant Neoplasm of Skin", "Malignant neoplasm of skin", "malignant neoplasm of skin", "Malignant skin neoplasm NOS", "Malignant Tumor of the Skin", "Malignant neoplasms of skin", "malignant neoplasm skin nos", "Skin neoplasm malignant NOS", "malignant tumor of the skin", "Skin malignant neoplasm NOS", "Malignant neoplasm of skin NOS", "Malignant Neoplasm of the Skin", "malignant neoplasm of the skin", "malignant zone of skin neoplasm", "skin cancer, Including melanoma", "Skin Cancer, Including Melanoma", "malignant neosplasm of the skin", "Malignant neoplasm of skin, NOS", "malignant neoplasm of zone of skin", "melanoma and Non-melanoma skin cancer", "Melanoma and Non-Melanoma Skin Cancer", "melanoma and non-melanoma skin cancer", "Malignant neoplasm of skin (disorder)", "malignant neoplasm of skin (diagnosis)", "Malignant neoplasm of skin, unspecified", "Skin neoplasms malignant and unspecified", "Skin cancer, nonmelanomatous (squamous and basal cell)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin cancer", "shortest_name_length": 11}
{"curie": "UMLS:C5204529", "names": ["Advanced Clear Cell Renal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Clear Cell Renal Cell Carcinoma", "shortest_name_length": 40}
{"curie": "UMLS:C5238509", "names": ["Trichoblastic Carcinosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Trichoblastic Carcinosarcoma", "shortest_name_length": 28}
{"curie": "UMLS:C0348321", "names": ["Hemophilus", "Haemophilus", "Hemophilus; influenzae", "Haemophilus; influenzae", "HEMOPHILUS INFLUENZA INFECTION", "Hemophilus Influenza Infection", "Hemophilus influenza infection", "hemophilus influenzae infection", "Hemophilus influenzae infection", "Haemophilus influenza infection", "HAEMOPHILUS INFLUENZA INFECTION", "Haemophilus influenzae infection", "haemophilus influenzae infection", "Haemophilus influenzae Infection", "infection; Hemophilus influenzae", "haemophilus infections influenzae", "infection; Haemophilus influenzae", "Infection, Haemophilus influenzae", "Haemophilus influenzae Infections", "Haemophilus influenzae infection, NOS", "Haemophilus influenzae infection (disorder)", "Hemophilus influenzae infection, unspecified", "haemophilus influenzae infection (diagnosis)", "Haemophilus influenzae infection, unspecified", "Hemophilus influenzae [H. influenzae] as the cause of diseases classified to other chapters", "Haemophilus influenzae [H. influenzae] as the cause of diseases classified to other chapters"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemophilus influenza infection", "shortest_name_length": 10}
{"curie": "MONDO:0056798", "names": ["APPENDIX DISEASE", "Disease;appendix", "appendix disease", "Appendix disorder", "appendix diseases", "Appendix Disorder", "appendix disorders", "appendiceal disease", "Disease of appendix", "disease of appendix", "Disorder of appendix", "disorder of appendix", "Diseases of appendix", "diseases of appendix", "Appendix disorder NOS", "disease of the appendix", "Disease of appendix, NOS", "DISEASES OF THE APPENDIX", "vermiform appendix disease", "disease of vermiform appendix", "disorder of vermiform appendix", "Diseases of appendix (K35-K38)", "Disorder of appendix (disorder)", "disease (or disorder); appendix", "Disease of appendix, unspecified", "disorder of appendix (diagnosis)", "vermiform appendix disease or disorder", "disease or disorder of vermiform appendix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of appendix", "shortest_name_length": 16}
{"curie": "MONDO:0004257", "names": ["childhood CNS mixed germ cell tumor", "Central nervous system Mixed germ cell tumor", "Central Nervous System Mixed Germ Cell Tumor", "Childhood Central Nervous System Mixed Germ Cell Tumor", "childhood central nervous system mixed germ cell tumor", "pediatric mixed germ cell tumor of central nervous system", "childhood mixed germ cell tumor of central nervous system", "mixed germ cell tumor of central nervous system of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood central nervous system mixed germ cell tumor", "shortest_name_length": 35}
{"curie": "UMLS:C4761284", "names": ["OSSN", "Conjunctival Squamous Neoplasia", "Ocular Surface Squamous Neoplasia", "Ocular surface squamous neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ocular surface squamous neoplasia", "shortest_name_length": 4}
{"curie": "MONDO:0007459", "names": ["hypopigmentation", "HYPOPIGMENTATION", "albinism, partial", "ALBINISM, PARTIAL", "dilution, pigmentary", "DILUTION, PIGMENTARY", "Dilution, Pigmentary", "hypomelanotic disorder", "Albinoidism, Oculocutaneous, Autosomal Dominant", "ALBINOIDISM, OCULOCUTANEOUS, AUTOSOMAL DOMINANT", "Albinoidism, oculocutaneous, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilution, pigmentary", "shortest_name_length": 16}
{"curie": "MONDO:0003531", "names": ["hidradenocarcinoma", "Hidradenocarcinoma", "sweat gland carcinoma", "tubular apocrine adenoma", "papillary eccrine adenoma", "Sweat gland adenocarcinoma", "Digital Papillary Carcinoma", "papillary eccrine carcinoma", "Papillary Eccrine Carcinoma", "Digital papillary carcinoma", "Clear Cell Eccrine Carcinoma", "adenocarcinoma of sweat gland", "malignant nodular hidradenoma", "Nodular hidradenoma, malignant", "papillary apocrine fibroadenoma", "Eccrine Papillary Adenocarcinoma", "Eccrine papillary adenocarcinoma", "Digital papillary adenocarcinoma", "eccrine papillary adenocarcinoma", "digital papillary adenocarcinoma", "Digital Papillary Adenocarcinoma", "Papillary digital eccrine carcinoma", "Papillary Digital Eccrine Carcinoma", "Digital Papillary Eccrine Carcinoma", "adenocarcinoma of sweat gland (diagnosis)", "Aggressive digital papillary adenocarcinoma", "Digital papillary eccrine carcinoma of skin", "Aggressive Digital Papillary Adenocarcinoma", "Sweat gland adenocarcinoma (morphologic abnormality)", "Digital papillary eccrine carcinoma of skin (disorder)", "Nodular hidradenoma, malignant (morphologic abnormality)", "Eccrine papillary adenocarcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papillary eccrine carcinoma", "shortest_name_length": 18}
{"curie": "MONDO:0017441", "names": ["phocomelia", "PHOCOMELIA", "Phocomelia", "Phocomelia NOS", "Phocomelia, NOS", "Phocomelic dwarf", "Dwarf, phocomelic", "Phocomelia (disorder)", "Phocomelia of unspecified limb", "Phocomelia, unspecified limb(s)", "Congenital absence of proximal portion of limb", "humero-radio-ulnar intercalary transverse meromelia", "congenital absence of upper arm and forearm with hand present"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital absence of upper arm and forearm with hand present", "shortest_name_length": 10}
{"curie": "MONDO:0017785", "names": ["PENS syndrome", "papular epidermal nevi with skyline basal cell layers syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PENS syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0020665", "names": ["High Grade Malignant Neoplasm", "high grade malignant neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "high grade malignant neoplasm", "shortest_name_length": 29}
{"curie": "MONDO:0054691", "names": ["CVID14", "common variable immunodeficiency 14", "immunodeficiency, common variable, 14", "IMMUNODEFICIENCY, COMMON VARIABLE, 14", "immunodeficiency, COMMON variable, 14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency, common variable, 14", "shortest_name_length": 6}
{"curie": "MONDO:0002188", "names": ["vulvar nodular hidradenoma", "Vulvar Nodular Hidradenoma", "mammalian vulva nodular hidradenoma", "nodular hidradenoma of mammalian vulva"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar nodular hidradenoma", "shortest_name_length": 26}
{"curie": "UMLS:C5206136", "names": ["HEMNOS", "HCN-NOS", "Hepatocellular Malignant Neoplasm, NOS", "Hepatocellular Malignant Neoplasm, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatocellular Malignant Neoplasm, Not Otherwise Specified", "shortest_name_length": 6}
{"curie": "UMLS:C4055379", "names": ["Bisphosphonate - Induced Nephropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bisphosphonate - Induced Nephropathy", "shortest_name_length": 36}
{"curie": "UMLS:C5557391", "names": ["Recurrent Higher Risk Myelodysplastic Syndrome", "Recurrent Higher-Risk Myelodysplastic Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Higher Risk Myelodysplastic Syndrome", "shortest_name_length": 46}
{"curie": "UMLS:C5447307", "names": ["Localized Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized Sarcoma", "shortest_name_length": 17}
{"curie": "UMLS:C4540534", "names": ["PITUITARY ADENOMA 3, MULTIPLE TYPES, SOMATIC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PITUITARY ADENOMA 3, MULTIPLE TYPES, SOMATIC", "shortest_name_length": 44}
{"curie": "UMLS:C4521740", "names": ["IA", "Stage IA Esophageal Squamous Cell Cancer", "Pathologic Stage IA Esophageal Squamous Cell Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IA Esophageal Squamous Cell Carcinoma AJCC v8", "shortest_name_length": 2}
{"curie": "MONDO:0013746", "names": ["VSD1", "VENTRICULAR SEPTAL DEFECT 1", "ventricular septal defect 1", "ventricular septal defect - VSD1", "ventricular septal defect type 1", "GATA4 ventricular septal defect (disease)", "ventricular septal defect - VSD1 (diagnosis)", "ventricular septal defect (disease) caused by mutation in GATA4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ventricular septal defect 1", "shortest_name_length": 4}
{"curie": "MONDO:0033352", "names": ["CHN", "neuropathy, congenital hypomelinating"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuropathy, congenital hypomelinating", "shortest_name_length": 3}
{"curie": "UMLS:C0162299", "names": ["THYROID CYST", "thyroid cyst", "cyst thyroid", "Thyroid cyst", "Thyroid Cyst", "cyst; thyroid", "cysts thyroid", "thyroid; cyst", "cyst of thyroid", "Cyst of Thyroid", "Cyst of thyroid", "of thyroid cyst", "Thyroid Gland Cyst", "Cyst of the Thyroid", "Cyst of Thyroid Gland", "thyroid cyst (diagnosis)", "Cyst of the Thyroid Gland", "Cyst of thyroid (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cyst of thyroid", "shortest_name_length": 12}
{"curie": "MONDO:0009067", "names": ["CSNU", "cystinuria", "CYSTINURIA", "Cystinuria", "Cystinurias", "CSNU1, FORMERLY", "CSNU3, FORMERLY", "Cystinuria, NOS", "CSNU - Cystinuria", "cystinuria, type I", "cystinuria, type a", "cystinuria, type B", "cystinuria, type II", "cystinuria-lysinuria", "Cystinuria, Type A-B", "cystinuria, type III", "cystinuria (disease)", "CYSTINURIA, TYPE A/B", "cystinuria, type A/B", "Cystinuria (disorder)", "cystinuria, type non-I", "cystinuria (diagnosis)", "High urine cystine levels", "cystinuria, type I, formerly", "CYSTINURIA, TYPE I, FORMERLY", "CYSTINURIA, TYPE II, FORMERLY", "cystinuria, type II, formerly", "cystinuria-lysinuria syndrome", "Cystinuria-lysinuria syndrome", "CYSTINURIA, TYPE III, FORMERLY", "cystinuria, type III, formerly", "CYSTINURIA, TYPE NON-I, FORMERLY", "cystinuria, type non-I, formerly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cystinuria", "shortest_name_length": 4}
{"curie": "MONDO:0011287", "names": ["CAP SYNDROME", "CAP syndrome", "CDAGS SYNDROME", "CDAGS syndrome", "craniosynostosis, anal anomalies, and porokeratosis", "CRANIOSYNOSTOSIS, ANAL ANOMALIES, AND POROKERATOSIS", "Craniosynostosis, anal anomalies, and porokeratosis", "Craniosynostosis, anal anomaly, porokeratosis syndrome", "craniosynostosis-anal anomalies-porokeratosis syndrome", "Craniosynostosis-anal anomalies-porokeratosis syndrome", "Craniosynostosis, anal anomaly, porokeratosis syndrome (disorder)", "craniosynostosis and clavicular hypoplasia, delayed closure of the fontanel, anal anomalies and genitourinary malformations", "CDAGS (craniosynostosis, clavicular hypoplasia, delayed closure of fontanelle, anal anomalies, genitourinary malformations, skin eruption) syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniosynostosis-anal anomalies-porokeratosis syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0005694", "names": ["Cecum Tumor", "cecum tumor", "caecum tumor", "Tumor of cecum", "cecal neoplasm", "Cecum Neoplasm", "Tumor of Cecum", "Cecal Neoplasm", "tumor of cecum", "cecum neoplasm", "Neoplasm, Cecal", "tumor of caecum", "caecum neoplasm", "Cecal Neoplasms", "Neoplasms, Cecal", "Tumour of caecum", "Neoplasm of cecum", "neoplasm of cecum", "Neoplasm of Cecum", "neoplasm of caecum", "tumor of the cecum", "Neoplasm of caecum", "Tumor of the Cecum", "neoplasm of the cecum", "Neoplasm of the Cecum", "cecal benign neoplasm", "caecum neoplasm (disease)", "Neoplasm of cecum (disorder)", "neoplasm of cecum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cecal neoplasm", "shortest_name_length": 11}
{"curie": "MONDO:0001737", "names": ["Neonatal Tetanus", "neonatal tetanus", "Tetanus neonatorum", "tetanus neonatorum", "Tetanus Neonatorum", "neonatorum; tetanus", "tetanus; neonatorum", "Tetanus neonatorum (disorder)", "tetanus neonatorum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tetanus neonatorum", "shortest_name_length": 16}
{"curie": "MONDO:0001100", "names": ["Macromastia", "macromastia", "large breast", "Large breast", "Gigantomastia", "gigantomastia", "enlarged breast", "Breasts enlarged", "breasts enlarged", "breast Hypertrophy", "Breast hypertrophy", "breast enlargement", "hypertrophy breast", "Hypertrophy breast", "Breast Hypertrophy", "Breast enlargement", "BREAST ENLARGEMENT", "breast hypertrophy", "breast enlargements", "hypertrophy; breast", "breast; hypertrophy", "enlargement; breast", "Mammary hypertrophy", "breast; enlargement", "mammary hypertrophy", "Hypertrophy of breast", "enlargement of breast", "hypertrophy of breast", "Hypertrophy of Breast", "Large breast (finding)", "Gigantomastia (disorder)", "Hypertrophy of breast NOS", "female breast enlargement", "Hypertrophy of the Breast", "hypertrophy of the breast", "Hypertrophy of the breasts", "Hypertrophy of breast, NOS", "breast enlargement females", "reported breast enlargement", "breast hypertrophy was seen", "breast enlargement (symptom)", "breast appearance hypertrophy", "large breast (physical finding)", "juvenile gigantomastia (subtype)", "Hypertrophy of breast (disorder)", "hypertrophy of breast (diagnosis)", "idiopathic gigantomastia (subtype)", "gestational gigantomastia (subtype)", "drug-induced gigantomastia (subtype)", "breast enlargement (physical finding)", "puberty-induced gigantomastia (subtype)", "hypertrophy of breast (physical finding)", "pregnancy-induced gigantomastia (subtype)", "medication-induced gigantomastia (subtype)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophy of breast", "shortest_name_length": 11}
{"curie": "MONDO:0023083", "names": ["epimetaphyseal dysplasia cataract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epimetaphyseal dysplasia cataract", "shortest_name_length": 33}
{"curie": "MONDO:0005445", "names": ["ponos", "PONOS", "Sahib", "Kala-azar", "Kala-Azar", "kala-azar", "Kala Azar", "kala azar", "KALA-AZAR", "azar kala", "Black Fever", "Assam fever", "dumdum fever", "Assam; fever", "Dumdum fever", "fever; Assam", "Fever, Black", "dumdum; fever", "MARD EL BICHA", "Burdwan fever", "fever; dumdum", "Dum Dum fever", "Dum-dum fever", "FEVER, DUMDUM", "Mard el bicha", "Burdwan; fever", "FEVER, BURDWAN", "fever; Burdwan", "Sirkari disease", "SIRKARI DISEASE", "viscus leishmaniasis", "Visceral leishmaniasis", "visceral leishmaniasis", "Leishmaniasis visceral", "leishmaniasis visceral", "visceral Leishmaniasis", "Visceral Leishmaniasis", "Leishmaniasis, visceral", "LEISHMANIASIS, VISCERAL", "Leishmaniasis, Visceral", "visceral; leishmaniasis", "leishmaniasis; visceral", "kala-azar susceptibility", "VL - Visceral leishmaniasis", "Mediterranean leishmaniasis", "kala-azar, susceptibility to", "Indian visceral leishmaniasis", "Leishmania donovani infection", "infection; Leishmania, donovani", "Leishmania; infection, donovani", "Infection by Leishmania donovani", "Visceral leishmaniasis (disorder)", "Infection by Leishmania, donovani", "Leishmaniasis visceral (kala-azar)", "Visceral [kala-azar] leishmaniasis", "visceral leishmaniasis (diagnosis)", "Infection by visceral leishmaniasis", "infection by visceral leishmaniasis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "visceral leishmaniasis", "shortest_name_length": 5}
{"curie": "UMLS:C1955743", "names": ["Mineralocorticoid deficiency", "mineralocorticoid deficiency", "Mineralocorticoid deficiency (disorder)", "mineralocorticoid deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mineralocorticoid deficiency", "shortest_name_length": 28}
{"curie": "UMLS:C4683611", "names": ["Lugano Classification Stage II Bulky Adult Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage II Bulky Adult Hodgkin Lymphoma AJCC v8", "shortest_name_length": 67}
{"curie": "UMLS:C4683624", "names": ["Stage C Chronic Lymphocytic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage C Chronic Lymphocytic Leukemia", "shortest_name_length": 36}
{"curie": "MONDO:0001559", "names": ["Perineocele", "perineocele", "Pelvic floor hernia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "perineocele", "shortest_name_length": 11}
{"curie": "MONDO:0019138", "names": ["bleeding diathesis due to a collagen receptor defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bleeding diathesis due to a collagen receptor defect", "shortest_name_length": 52}
{"curie": "UMLS:C5208195", "names": ["Male reproductive tract disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Male reproductive tract disorder", "shortest_name_length": 32}
{"curie": "UMLS:C0278519", "names": ["recurrent childhood", "recurrent pediatric", "Relapsed Childhood ALL", "relapsed childhood ALL", "relapsed pediatric ALL", "Relapsed Pediatric ALL", "Recurrent Childhood ALL", "childhood ALL, relapsed", "recurrent childhood ALL", "Recurrent Pediatric ALL", "pediatric ALL, relapsed", "recurrent pediatric ALL", "pediatric ALL, recurrent", "ALL, relapsed, childhood", "ALL, childhood, relapsed", "childhood ALL, recurrent", "ALL, relapsed, pediatric", "ALL, pediatric, relapsed", "ALL, recurrent, childhood", "ALL, recurrent, pediatric", "relapsed pediatric acute lymphoid leukemia", "Relapsed Pediatric Acute Lymphoid Leukemia", "Recurrent Pediatric Acute Lymphoid Leukemia", "Recurrent Childhood Acute Lymphoid Leukemia", "recurrent childhood acute lymphoid leukemia", "recurrent pediatric acute lymphoid leukemia", "Recurrent Acute Lymphoblastic Leukemia (ALL)", "Relapsed Childhood Acute Lymphocytic Leukemia", "relapsed childhood acute lymphocytic leukemia", "relapsed pediatric acute lymphocytic leukemia", "Relapsed Pediatric Acute Lymphocytic Leukemia", "Recurrent Childhood Acute Lymphocytic Leukemia", "relapsed pediatric acute lymphogenous leukemia", "pediatric acute lymphocytic leukemia, relapsed", "Relapsed Pediatric Acute Lymphogenous Leukemia", "recurrent pediatric acute lymphocytic leukemia", "childhood acute lymphocytic leukemia, relapsed", "Recurrent Pediatric Acute Lymphocytic Leukemia", "relapsed pediatric acute lymphoblastic leukemia", "Recurrent Pediatric Acute Lymphogenous Leukemia", "Relapsed Pediatric Acute Lymphoblastic Leukemia", "Relapsed Childhood Acute Lymphoblastic Leukemia", "acute lymphocytic leukemia, childhood, relapsed", "Recurrent Childhood Acute Lymphogenous Leukemia", "relapsed childhood acute lymphoblastic leukemia", "recurrent childhood acute lymphogenous leukemia", "recurrent pediatric acute lymphogenous leukemia", "recurrent pediatric acute lymphoblastic leukemia", "Recurrent Childhood Acute Lymphoblastic Leukemia", "lymphocytic leukemia, acute, childhood, relapsed", "leukemia, acute lymphocytic, childhood, relapsed", "Recurrent Pediatric Acute Lymphoblastic Leukemia", "recurrent childhood acute lymphoblastic leukemia", "recurrent childhood precursor lymphoblastic leukemia", "Recurrent Childhood Precursor Lymphoblastic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Acute Lymphoblastic Leukemia", "shortest_name_length": 19}
{"curie": "MONDO:0033199", "names": ["DFNB107", "DEAFNESS, AUTOSOMAL RECESSIVE 107", "deafness, autosomal recessive 107", "hearing loss, autosomal recessive 107", "autosomal recessive nonsyndromic deafness 107"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal recessive 107", "shortest_name_length": 7}
{"curie": "MONDO:0013481", "names": ["del(13q14)", "Del(13)(q14)", "del(13)(q14)", "monosomy 13q14", "deletion 13q14", "monosomy type 13q14", "CHROMOSOME 13q DELETION SYNDROME", "chromosome 13Q deletion syndrome", "Chromosome 13q14 deletion syndrome", "CHROMOSOME 13q14 DELETION SYNDROME", "chromosome 13q14 deletion syndrome", "chromosome 13q14 deletion syndrome, isolated cases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 13q14 deletion syndrome", "shortest_name_length": 10}
{"curie": "MONDO:0013480", "names": ["HOMG6", "renal hypomagnesemia-6", "renal hypomagnesemia 6", "hypomagnesemia 6, renal", "HYPOMAGNESEMIA 6, RENAL", "renal hypomagnesemia type 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal hypomagnesemia 6", "shortest_name_length": 5}
{"curie": "MONDO:0001522", "names": ["pyromania", "Pyromania", "PYROMANIA", "Pyromanias", "Firesetting", "firesetting", "fire setting", "SETTING FIRES", "setting fires", "Setting fires", "fire settings", "Firesetting Behavior", "firesetting behavior", "Firesetting behavior", "Pyromania (disorder)", "pyromania (diagnosis)", "Behavior, Firesetting", "Firesetting Behaviors", "Firesetting behaviour", "Firesetting (finding)", "Behaviors, Firesetting", "setting fires (symptom)", "pathological firesetting", "pathologic; fire-setting", "Pathological firesetting", "Pathological fire-setting", "fire-setting; pathological", "Pathological fire-setting [pyromania]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyromania", "shortest_name_length": 9}
{"curie": "MONDO:0032791", "names": ["CSS10", "IDDSDF", "COFFIN-SIRIS SYNDROME 10", "Coffin-Siris syndrome 10", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY AND DYSMORPHIC FACIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Coffin-Siris syndrome 10", "shortest_name_length": 5}
{"curie": "MONDO:0017213", "names": ["POIS", "post orgasmic sick syndrome", "postorgasmic illness syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postorgasmic illness syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0020920", "names": ["E COLI INFECT", "INFECT E COLI", "colibacillosis", "Colibacillosis", "E coli infection", "coli e infection", "Infection;E coli", "E Coli Infection", "E COLI INFECTION", "e coli infection", "Escherichia coli", "E coli Infection", "e. coli infection", "coli e. infection", "Infection, E coli", "E coli infections", "E coli Infections", "coli e infections", "E. coli Infection", "infections e coli", "E. coli infection", "Infections, E coli", "E. coli Infections", "E. coli infections", "E. Coli Infections", "Infection, E. coli", "INFECT ESCHERICHIA COLI", "ESCHERICHIA COLI INFECT", "Escherichia Coli Infection", "Escherichia coli Infection", "escherichia coli infection", "Escherichia coli infection", "escherichia coli infections", "Escherichia coli Infections", "Infection, Escherichia coli", "ESCHERICHIA COLI INFECTIONS", "Escherichia coli infections", "Recurrent E. coli infections", "E coli infections, recurrent", "Infections, Escherichia coli", "Other and unspecified E. coli", "Escherichia coli [E. coli] NOS", "Infection due to Escherichia coli", "Bacterial infection due to E. coli", "Infection caused by Escherichia coli", "Bacterial infection caused by E. coli", "Infection due to Escherichia coli, NOS", "Escherichia coli infection (diagnosis)", "Other and unspecified Escherichia coli", "Bacterial infection due to E. coli, NOS", "Infection caused by Escherichia coli (disorder)", "Other and unspecified Escherichia coli [E. coli]", "Unspecified Escherichia coli [E. coli] as the cause of diseases classified elsewhere"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "escherichia coli infection", "shortest_name_length": 13}
{"curie": "MONDO:0009666", "names": ["HLCS DEFICIENCY", "HLCS Deficiency", "HLCS deficiency", "Deficiency, HLCS", "HLCS Deficiencies", "Deficiencies, HLCS", "Multiple Carboxylase Deficiency", "multiple carboxylase deficiency", "holocarboxylase synthase deficiency", "Holocarboxylase synthase deficiency", "Holoocarboxylase synthase deficiency", "holocarboxylase synthetase deficiency", "Holocarboxylase Synthetase Deficiency", "HOLOCARBOXYLASE SYNTHETASE DEFICIENCY", "Holocarboxylase synthetase deficiency", "Deficiency, Holocarboxylase Synthetase", "Holocarboxylase Synthetase Deficiencies", "Neonatal Multiple Carboxylase Deficiency", "neonatal multiple carboxylase deficiency", "Neonatal multiple carboxylase deficiency", "Deficiencies, Holocarboxylase Synthetase", "Infantile Multiple Carboxylase Deficiency", "Early-Onset Combined Carboxylase Deficiency", "Early Onset Combined Carboxylase Deficiency", "Early-onset multiple carboxylase deficiency", "early-onset multiple carboxylase deficiency", "MULTIPLE CARBOXYLASE DEFICIENCY, EARLY ONSET", "Multiple Carboxylase Deficiency, Early Onset", "multiple carboxylase deficiency, early onset", "Holocarboxylase synthase deficiency (disorder)", "Neonatal Holocarboxylase Synthetase Deficiency", "MULTIPLE CARBOXYLASE DEFICIENCY, NEONATAL FORM", "multiple carboxylase deficiency, neonatal form", "Multiple Carboxylase Deficiency, Neonatal Form", "Carboxylase Deficiency, Multiple, Neonatal Form", "Deficiency, Multiple Carboxylase, Neonatal Form", "holocarboxylase synthase deficiency (diagnosis)", "multiple carboxylase deficiency - neonatal onset", "Multiple carboxylase deficiency - neonatal onset", "biotin-(propionyl-CoA-carboxylase) ligase deficiency", "Biotin-(propionyl-CoA-carboxylase) ligase deficiency", "Neonatal biotin-responsive multiple carboxylase deficiency", "Early Onset Biotin Responsive Multiple Carboxylase Deficiency", "Early-Onset Biotin-Responsive Multiple Carboxylase Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "holocarboxylase synthetase deficiency", "shortest_name_length": 15}
{"curie": "MONDO:0044786", "names": ["Frantz tumor", "Frantz Tumor", "solid pseudopapillary tumor of pancreas", "solid pseudopapillary pancreatic neoplasm", "Solid Pseudopapillary Tumor of the Pancreas", "solid pseudopapillary tumor of the pancreas", "Solid pseudopapillary tumor of the pancreas", "Solid pseudopapillary tumour of the pancreas", "Solid Pseudopapillary Neoplasm of the Pancreas", "solid pseudopapillary neoplasm of the pancreas", "solid pseudopapillary tumor of pancreas (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "solid pseudopapillary neoplasm of the pancreas", "shortest_name_length": 12}
{"curie": "MONDO:0008599", "names": ["TN", "Tic Doloureux", "Tic douloureux", "tic douloureux", "TIC DOULOUREUX", "Tic Douleureux", "Tic Douloureux", "tic; douloureux", "douloureux; tic", "pain; trigeminal", "trigeminal; pain", "fothergill disease", "trifocal neuralgia", "Fothergill Disease", "FOTHERGILL DISEASE", "Trifocal neuralgia", "trifacial neuralgia", "Trifacial neuralgia", "Disease, Fothergill", "Trifacial Neuralgia", "trigeminal neuralgia", "neuralgia; trifacial", "Trigeminal neuralgia", "trifacial; neuralgia", "NEURALGIA TRIGEMINAL", "Trigeminal Neuralgia", "Trigeminus neuralgia", "TRIGEMINAL NEURALGIA", "Trifacial Neuralgias", "trigeminus neuralgia", "Neuralgia trigeminal", "Neuralgia, Trifacial", "Neuralgia, Trigeminal", "Fothergill; neuralgia", "trigeminal; neuralgia", "neuralgia; Fothergill", "Trigeminal Neuralgias", "NEURALGIA, TRIGEMINAL", "neuralgia; trigeminal", "Epileptiform Neuralgia", "Fothergill's neuralgia", "Neuralgia, Epileptiform", "Epileptiform Neuralgias", "Trigeminal neuralgia NOS", "Trigeminal neuralgia, NOS", "TN - Trigeminal neuralgia", "trigeminal nerve neuralgia", "neuralgia of trigeminal nerve", "Trigeminal neuralgia syndrome", "Trigeminal neuralgia (disorder)", "Trigeminal neuralgia (diagnosis)", "trigeminal neuralgia; Fothergill", "Fothergill; trigeminal neuralgia", "cranial nerve; neuralgia, fifth or trigeminal", "neuralgia; cranial nerve, fifth or trigeminal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trigeminal neuralgia", "shortest_name_length": 2}
{"curie": "MONDO:0001983", "names": ["Peripheral corneal degeneration", "peripheral corneal degeneration", "peripheral degeneration of cornea", "Peripheral degeneration of cornea", "peripheral degenerations of cornea", "Peripheral degenerations of cornea", "peripheral corneal degeneration (diagnosis)", "Peripheral degeneration of cornea (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peripheral degeneration of cornea", "shortest_name_length": 31}
{"curie": "MONDO:0032848", "names": ["IMD65", "immunodeficiency 65", "immunodeficiency 65, susceptibility to viral infections", "IMMUNODEFICIENCY 65, SUSCEPTIBILITY TO VIRAL INFECTIONS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 65, susceptibility to viral infections", "shortest_name_length": 5}
{"curie": "MONDO:0016690", "names": ["PXA", "pleomorphic xanthoastrocytoma", "Pleomorphic xanthoastrocytoma", "Pleomorphic Xanthoastrocytoma", "pleomorphic Xantho-astrocytoma", "Pleomorphic Xantho-Astrocytoma", "Pleomorphic Xantho-astrocytoma", "[M] Pleomorphic xanthoastrocytoma", "Pleomorphic xanthoastrocytoma (disorder)", "Pleomorphic xanthoastrocytoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pleomorphic xanthoastrocytoma", "shortest_name_length": 3}
{"curie": "UMLS:C4725672", "names": ["Refractory Osteomedullary Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Osteomedullary Disease", "shortest_name_length": 33}
{"curie": "UMLS:C4526721", "names": ["Stage III", "Stage III Lung Cancer", "Stage III Lung Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Lung Cancer AJCC v8", "shortest_name_length": 9}
{"curie": "MONDO:0010083", "names": ["SSADH", "SSADHD", "GABAuria", "SSADH Deficiency", "Ssadh deficiency", "SSADH DEFICIENCY", "SSADH deficiency", "GABA metabolic defect", "GABA METABOLIC DEFECT", "4-Hydroxybutyricaciduria", "4-Hydroxybutyric aciduria", "4 hydroxybutyric aciduria", "4-hydroxybutyric aciduria", "4-HYDROXYBUTYRIC ACIDURIA", "4--Hydroxybutyric aciduria", "gamma-hydroxybutyricaciduria", "GAMMA-HYDROXYBUTYRIC ACIDURIA", "Gamma-Hydroxybutyric Aciduria", "gamma-Hydroxybutyric aciduria", "Gamma-hydroxybutyric acidemia", "Gamma-Hydroxybutyric Acidemia", "gamma-hydroxybutyric aciduria", "Gamma-hydroxybutyric aciduria", "Gamma-hydroxybutyric acidaemia", "4-hydroxybutyric aciduria (diagnosis)", "gamma-hydroxybutyric aciduria (diagnosis)", "succinic semialdehyde dehydrogenase deficiency", "SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY", "Succinic semialdehyde dehydrogenase deficiency", "Succinate-semialdehyde dehydrogenase deficiency", "succinate-semialdehyde dehydrogenase deficiency", "succinic semialdehyde dehydrogenase deficiency (diagnosis)", "Succinate-semialdehyde dehydrogenase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "succinic semialdehyde dehydrogenase deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C0919666", "names": ["Venipuncture site hemorrhage", "Venipuncture site haemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Venipuncture site haemorrhage", "shortest_name_length": 28}
{"curie": "UMLS:C0879615", "names": ["stromal tumor", "tumor stromal", "Stromal tumor", "Stromal Tumor", "stromal tumour", "tumors stromal", "Stromal tumour", "stromal tumors", "stromal tumours", "Stromal Neoplasm", "Stromal tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stromal Neoplasm", "shortest_name_length": 13}
{"curie": "MONDO:0021008", "names": ["secondary antiphospholipid syndrome", "Secondary antiphospholipid syndrome", "antiphospholipid antibody syndrome secondary", "Secondary antiphospholipid syndrome (disorder)", "Secondary antiphospholipid syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary antiphospholipid syndrome", "shortest_name_length": 35}
{"curie": "UMLS:C0522618", "names": ["Focal Dysplasia", "Focal dysplasia", "Focal dysplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Focal dysplasia", "shortest_name_length": 15}
{"curie": "UMLS:C0279973", "names": ["stage III ovarian germ cell tumor", "Stage III Ovarian Germ Cell Tumor", "ovarian germ cell tumor, stage III", "germ cell tumor, ovarian, stage III", "Stage III Ovarian Germ Cell Tumor AJCC v6", "Stage III Ovarian Germ Cell Tumor AJCC v7", "Stage III Malignant Ovarian Germ Cell Tumor", "Stage III Malignant Germ Cell Tumor of Ovary", "Stage III Malignant Ovarian Germ Cell Neoplasm", "Stage III Malignant Germ Cell Neoplasm of Ovary", "Stage III Ovarian Germ Cell Tumor AJCC v6 and v7", "Stage III Malignant Germ Cell Tumor of the Ovary", "Stage III Malignant Germ Cell Neoplasm of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Ovarian Germ Cell Tumor AJCC v6 and v7", "shortest_name_length": 33}
{"curie": "UMLS:C0740913", "names": ["Dog Allergy", "allergy dog", "Dog allergy", "Allergy, Dog", "allergy dogs", "allergies dog", "allergies dogs", "ALLERGY TO DOGS", "allergy to dogs", "allergic to dogs", "Allergic to dogs", "allergy to dogs (history)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dog Allergy", "shortest_name_length": 11}
{"curie": "UMLS:C0349782", "names": ["CARDIOMYOPATHY ISCHEMIC", "ischemic cardiomyopathy", "cardiomyopathy ischemic", "Ischemic cardiomyopathy", "cardiomyopathy; ischemic", "ischemic; cardiomyopathy", "Ischaemic cardiomyopathy", "ischaemic cardiomyopathy", "Generalized ischemic myocardial dysfunction", "generalized ischemic myocardial dysfunction", "Generalised ischaemic myocardial dysfunction", "Generalized ischemic myocardial dysfunction (disorder)", "generalized ischemic myocardial dysfunction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ischemic cardiomyopathy", "shortest_name_length": 23}
{"curie": "MONDO:0018734", "names": ["hemangioma verrucous", "Verrucous hemangioma", "verrucous hemangioma", "Verrucous Hemangioma", "Verrucous Venous Malformation", "Verrucous keratotic hemangioma", "verrucous keratotic hemangioma", "Verrucous Keratotic Hemangioma", "hemangioma; verrucous keratotic", "Verrucous keratotic haemangioma", "verrucous; keratotic hemangioma", "verrucous; hemangioma, keratotic", "verrucous hemangioma (physical finding)", "Verrucous keratotic hemangioma (morphologic abnormality)", "verrucous keratotic hemangioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "verrucous hemangioma", "shortest_name_length": 20}
{"curie": "MONDO:0021464", "names": ["benign cecum tumor", "Benign Cecum Tumor", "Benign Cecum Neoplasm", "benign cecum neoplasm", "Benign tumor of cecum", "Benign Tumor of Cecum", "benign tumor of cecum", "caecum benign neoplasm", "Benign tumour of caecum", "Benign Neoplasm of Cecum", "benign neoplasm of cecum", "Benign neoplasm of cecum", "Benign Tumor of the Cecum", "Benign neoplasm of caecum", "benign tumor of the cecum", "Benign Neoplasm of the Cecum", "benign neoplasm of the cecum", "Benign neoplasm of cecum (disorder)", "benign neoplasm of cecum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of cecum", "shortest_name_length": 18}
{"curie": "UMLS:C1332467", "names": ["Benign Adult Brainstem Tumor", "Benign Adult Brain Stem Tumor", "Benign Adult Brainstem Tumors", "Benign Adult Brain Stem Tumors", "Benign Tumor of Adult Brainstem", "Benign Adult Brainstem Neoplasm", "Benign Adult Brainstem Neoplasms", "Benign Adult Brain Stem Neoplasm", "Benign Tumor of Adult Brain Stem", "Adult Benign Brain Stem Neoplasms", "Benign Neoplasm of Adult Brainstem", "Benign Neoplasm of Adult Brain Stem", "Benign Tumor of the Adult Brainstem", "Benign Tumor of the Adult Brain Stem", "Benign Neoplasm of the Adult Brainstem", "Benign Neoplasm of the Adult Brain Stem"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Adult Brain Stem Neoplasm", "shortest_name_length": 28}
{"curie": "MONDO:0054561", "names": ["ANXD2", "anauxetic dysplasia 2", "ANAUXETIC DYSPLASIA 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anauxetic dysplasia 2", "shortest_name_length": 5}
{"curie": "MONDO:0008214", "names": ["PHA", "pelger huet anomaly", "Pelger-Huet Anomaly", "Pelger-Huët Anomaly", "PELGER-HUET ANOMALY", "pelger-huet anomaly", "Pelger Huet Anomaly", "anomaly huet pelger", "Pelger Huet anomaly", "Pelger-Huët anomaly", "Pelger Huët Anomaly", "Pelger-Huet anomaly", "Pelger-Huet; anomaly", "anomaly; Pelger-Huet", "Anomaly, Pelger-Huet", "Anomaly, Pelger-Huët", "Pelger Huet Nuclear Anomaly", "Pelger-Huët Nuclear Anomaly", "Pelger-Huet Nuclear Anomaly", "Pelger-Huet nuclear anomaly", "Pelger Huët Nuclear Anomaly", "Anomaly, Pelger-Huet Nuclear", "Anomaly, Pelger-Huët Nuclear", "Nuclear Anomaly, Pelger-Huët", "Nuclear Anomaly, Pelger-Huet", "Pelger-Huët anomaly (disorder)", "Pelger-Huet anomaly (diagnosis)", "Hyposegmentation of neutrophil nuclei", "Hyposegmentation of neutrophil nuclei in peripheral blood", "Ovoid Neutrophil Nuclei, Developmental Delay, Epilepsy and Skeletal Abnormalities", "ovoid neutrophil nuclei, developmental delay, epilepsy and skeletal abnormalities", "Ovoid Neutrophil Nuclei, Developmental Delay, Epilepsy, and Skeletal Abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pelger-Huet anomaly", "shortest_name_length": 3}
{"curie": "UMLS:C5239034", "names": ["Lumbar Spine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lumbar Spine Neoplasm", "shortest_name_length": 21}
{"curie": "UMLS:C4331344", "names": ["Stage IVB Nasopharyngeal Throat Cancer", "Stage IVB Nasopharyngeal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Nasopharyngeal Carcinoma AJCC v8", "shortest_name_length": 38}
{"curie": "UMLS:C4727948", "names": ["Hypermutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypermutation", "shortest_name_length": 13}
{"curie": "MONDO:0018254", "names": ["spondyloepimetaphyseal dysplasia, Isidor type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepimetaphyseal dysplasia, Isidor type", "shortest_name_length": 45}
{"curie": "UMLS:C4745068", "names": ["Maternally Derived GVHD", "Maternally Derived Graft Versus Host Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Maternally Derived Graft Versus Host Disease", "shortest_name_length": 23}
{"curie": "MONDO:0004730", "names": ["speech defect", "Speech defect", "speech; defect", "defects speech", "Speech defects", "defect; speech", "Abnormal speech", "speech disorder", "Speech Disorder", "disorder speech", "Speech disorder", "Disorder speech", "DISORDER SPEECH", "SPEECH DISORDER", "speech disorders", "Speech disorders", "Speech Disorders", "disorders speech", "Speech impediment", "defective; speech", "Speech impairment", "DEFECT SPEECH (NOS)", "Abnormal vocalization", "Neurological speech impairment", "speech impediment or impairment", "Speech impediment or impairment", "Abnormality of speech or vocalization"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "speech disorder", "shortest_name_length": 13}
{"curie": "UMLS:C4688333", "names": ["Childhood Recurrent Malignant Solid Tumor", "Recurrent Childhood Malignant Solid Neoplasm", "Childhood Recurrent Malignant Solid Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Recurrent Malignant Solid Neoplasm", "shortest_name_length": 41}
{"curie": "MONDO:0040872", "names": ["idiopathic polydipsia", "non-psychogenic polydipsia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-psychogenic polydipsia", "shortest_name_length": 21}
{"curie": "UMLS:C1266133", "names": ["Genital rhabdomyoma", "Genital Rhabdomyoma", "Genital type rhabdomyoma", "Genital rhabdomyoma (disorder)", "Genital rhabdomyoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Genital rhabdomyoma", "shortest_name_length": 19}
{"curie": "MONDO:0021663", "names": ["epidermoid spindle cell carcinoma", "Epidermoid Spindle Cell Carcinoma", "Epidermoid carcinoma, spindle cell", "Sarcomatoid Squamous Cell Carcinoma", "sarcomatoid squamous cell carcinoma", "Squamous Cell Spindle Cell Carcinoma", "squamous cell spindle cell carcinoma", "Squamous Cell Carcinoma, Sarcomatoid", "squamous cell carcinoma, sarcomatoid", "Spindle Cell Squamous Cell Carcinoma", "Squamous cell carcinoma, sarcomatoid", "squamous cell carcinoma, spindle cell", "Squamous Cell Carcinoma, Spindle Cell", "Squamous cell carcinoma, spindle cell", "Squamous Cell Carcinoma, Spindle Cell Variant", "spindle cell (sarcomatoid) squamous cell carcinoma", "Spindle Cell (Sarcomatoid) Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sarcomatoid squamous cell carcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C0334290", "names": ["Carcinoma In Situ in a Polyp", "Carcinoma in situ in a polyp", "Carcinoma in situ in a polyp, NOS", "Carcinoma in situ in adenomatous polyp", "Adenocarcinoma In Situ in Tubular Adenoma", "Adenocarcinoma in situ in tubular adenoma", "Adenocarcinoma in situ in polypoid adenoma", "Adenocarcinoma In Situ in Adenomatous Polyp", "Adenocarcinoma in situ in adenomatous polyp", "adenocarcinoma in situ in adenomatous polyp", "[M] Adenocarcinoma in situ in adenomatous polyp", "adenocarcinoma in situ in adenomatous polyp (diagnosis)", "Adenocarcinoma in situ in adenomatous polyp (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma in situ in adenomatous polyp", "shortest_name_length": 28}
{"curie": "MONDO:0010033", "names": ["PSS1", "generalized PSS", "Generalized PSS", "peeling skin syndrome 1", "Generalized deciduous skin", "generalized deciduous skin", "peeling skin syndrome type 1", "Generalised peeling skin syndrome", "Generalized peeling skin syndrome", "generalized peeling skin syndrome", "Generalized peeling skin syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "generalized peeling skin syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0857751", "names": ["Erythema multiforme minor", "Erythema Multiforme Minor", "erythema multiforme minor", "erythema multiforme, minor", "Erythema multiforme minor NOS", "Erythema multiforme minor (disorder)", "erythema multiforme minor (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Erythema multiforme minor", "shortest_name_length": 25}
{"curie": "MONDO:0025986", "names": ["megacystis-microcolon-intestinal hypoperistalsis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "megacystis-microcolon-intestinal hypoperistalsis syndrome", "shortest_name_length": 57}
{"curie": "MONDO:0003811", "names": ["ovarian seromucinous tumor", "Ovarian Seromucinous Tumor", "ovarian Seromucinous tumor", "Ovarian mixed epithelial tumor", "ovarian mixed epithelial tumor", "mixed epithelial tumor of ovary", "Ovarian mixed epithelial tumour", "Mixed epithelial tumor of ovary", "mixed epithelial tumour of ovary", "Mixed epithelial tumour of ovary", "ovarian neoplasm epithelial mixed", "ovarian mixed epithelial neoplasm", "mixed epithelial neoplasm of ovary", "mixed epithelial tumor of the ovary", "mixed epithelial neoplasm of the ovary", "Mixed epithelial tumor of ovary (disorder)", "mixed epithelial neoplasm of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian seromucinous tumor", "shortest_name_length": 26}
{"curie": "MONDO:0006599", "names": ["HIVES, PHYSICAL", "Urticaria physical", "physical urticaria", "Physical urticaria", "URTICARIA, PHYSICAL", "Physical urticaria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "physical urticaria", "shortest_name_length": 15}
{"curie": "MONDO:0004346", "names": ["signet Ring cell intrahepatic cholangiocarcinoma", "signet ring cell intrahepatic cholangiocarcinoma", "Signet Ring Cell Intrahepatic Cholangiocarcinoma", "Signet-Ring Cell Intrahepatic Cholangiocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "signet ring cell intrahepatic cholangiocarcinoma", "shortest_name_length": 48}
{"curie": "UMLS:C0751374", "names": ["Plexiform Schwannomatoses", "Plexiform Schwannomatosis", "Schwannomatosis, Plexiform"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Schwannomatosis, Plexiform", "shortest_name_length": 25}
{"curie": "UMLS:C5420225", "names": ["Oral Cavity Soft Tissue Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral Cavity Soft Tissue Neoplasm", "shortest_name_length": 32}
{"curie": "UMLS:C1708180", "names": ["Gallbladder Tubular Adenoma", "tubular adenoma of gallbladder", "tubular adenoma of gallbladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tubular adenoma of gallbladder", "shortest_name_length": 27}
{"curie": "MONDO:0019901", "names": ["non-distal monosomy 20q", "non-distal deletion 20q", "non-telomeric monosomy 20q", "non-distal monosomy type 20q"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-distal monosomy 20q", "shortest_name_length": 23}
{"curie": "UMLS:C5419813", "names": ["Liver Neuroendocrine Tumor G3", "Hepatic Neuroendocrine Tumor G3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liver Neuroendocrine Tumor G3", "shortest_name_length": 29}
{"curie": "UMLS:C1336436", "names": ["Stage IV Renal Pelvis Cancer", "Stage IV Renal Pelvis Carcinoma", "Stage IV Carcinoma of Renal Pelvis", "Stage IV Renal Pelvis Cancer AJCC v7", "Stage IV Carcinoma of the Renal Pelvis", "Stage IV Renal Pelvis Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Renal Pelvis Cancer AJCC v7", "shortest_name_length": 28}
{"curie": "UMLS:C1336206", "names": ["fallopian tube cancer stage IIIA", "stage IIIA fallopian tube cancer", "Stage IIIA Fallopian Tube Cancer", "Fallopian Tube Cancer Stage IIIA", "AJCC stage IIIA fallopian tube cancer", "AJCC Stage IIIA Fallopian Tube Cancer", "FIGO Stage IIIA Fallopian Tube Carcinoma", "stage IIIA fallopian tube cancer AJCC v7", "Stage IIIA Fallopian Tube Cancer AJCC v7", "FIGO stage IIIA fallopian tube carcinoma", "FIGO Stage IIIA Carcinoma of Fallopian Tube", "FIGO stage IIIA carcinoma of fallopian tube", "FIGO stage IIIA carcinoma of the fallopian tube", "FIGO Stage IIIA Carcinoma of the Fallopian Tube"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Fallopian Tube Cancer AJCC v7", "shortest_name_length": 32}
{"curie": "UMLS:C5206580", "names": ["Testicular Plasmacytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular Plasmacytoma", "shortest_name_length": 23}
{"curie": "MONDO:0002468", "names": ["hyperimmunoglobulin syndrome", "Hyperimmunoglobulin Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperimmunoglobulin syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0020682", "names": ["EDSSLA", "EDSSPD1", "EDSP1, FORMERLY", "XGPT DEFICIENCY", "XGPT deficiency", "dermatan sulfate proteoglycan", "DERMATAN SULFATE PROTEOGLYCAN", "PDS, DEFECTIVE BIOSYNTHESIS OF", "PDS, defective biosynthesis of", "galactosyltransferase 1 deficiency", "GALACTOSYLTRANSFERASE I DEFICIENCY", "Galactosyltransferase I deficiency", "Galactosyltransferase I Deficiency", "Galactosyltransferase 1 deficiency", "Ehlers-Danlos syndrome, progeroid form", "Ehlers-Danlos syndrome, progeroid type 1", "Ehlers-Danlos syndrome, progeroid type, 1", "Progeroid variant of Ehlers-Danlos syndrome", "Defective biosynthesis of proteodermatan sulfate", "Ehlers-Danlos syndrome spondylodysplastic type 1", "Proteodermatan sulfate, defective biosynthesis of", "PROTEODERMATAN SULFATE, DEFECTIVE BIOSYNTHESIS OF", "proteodermatan sulfate, defective biosynthesis of", "Defective biosynthesis of proteodermatan sulphate", "Ehlers-Danlos syndrome, spondylodysplastic type, 1", "EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1", "Ehlers-Danlos syndrome, progeroid type, 1, formerly", "EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 1, FORMERLY", "Xylosylprotein 4-beta-galactosyltransferase deficiency", "XYLOSYLPROTEIN 4-BETA-GALACTOSYLTRANSFERASE DEFICIENCY", "xylosylprotein 4-Beta-galactosyltransferase deficiency", "EHLERS-DANLOS SYNDROME WITH SHORT STATURE AND LIMB ANOMALIES", "Ehlers-Danlos syndrome with Short stature and Limb anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ehlers-Danlos syndrome, spondylodysplastic type, 1", "shortest_name_length": 6}
{"curie": "MONDO:0009985", "names": ["rhe syndrome", "RHE SYNDROME", "RHE syndrome", "RETINOHEPATOENDOCRINOLOGIC SYNDROME", "retinohepatoendocrinologic syndrome", "Retinohepatoendocrinologic syndrome", "Retinohepatoendocrinologic Syndrome", "RHE (retinohepatoendocrinologic) syndrome", "Retinohepatoendocrinologic syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinohepatoendocrinologic syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0014963", "names": ["SHAPNS", "Shashi-Pena syndrome", "SHASHI-PENA SYNDROME", "Shashi-Pena syndrome; SHAPNS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Shashi-Pena syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0010369", "names": ["NYS5", "congenital nystagmus 5", "X-linked congenital nystagmus 5", "NYSTAGMUS 5, CONGENITAL, X-LINKED", "nystagmus 5, congenital, X-linked", "NYSTAGMUS 5, congenital, X-linked", "Nystagmus 5, Infantile Periodic Alternating", "nystagmus 5, congenital, X-linked, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nystagmus 5, congenital, X-linked", "shortest_name_length": 4}
{"curie": "MONDO:0001386", "names": ["Seizures", "visual seizure", "Visual seizure", "Visual Seizure", "seizure visual", "Visual Epilepsy", "Visual Seizures", "epilepsy visual", "visual epilepsy", "Visual epilepsy", "Seizure, Visual", "Epilepsy, visual", "epilepsy; visual", "epilepsy, visual", "Seizures, Visual", "visual; epileptic", "Hallucination seizure", "Seizure, hallucination", "Visual epilepsy (disorder)", "visual partial simple seizure", "visual partial simple seizure (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "visual epilepsy", "shortest_name_length": 8}
{"curie": "MONDO:0021524", "names": ["Benign Buccal Mucosa Tumor", "benign buccal mucosa tumor", "Benign tumor of cheek mucosa", "benign buccal mucosa neoplasm", "Benign Tumor of Buccal Mucosa", "Benign Buccal Mucosa Neoplasm", "benign tumor of buccal mucosa", "buccal mucosa benign neoplasm", "Benign tumour of cheek mucosa", "Benign tumor of buccal mucosa", "Benign tumor of internal cheek", "Benign tumour of buccal mucosa", "Benign tumour of internal cheek", "Benign neoplasm of cheek mucosa", "Benign neoplasm of buccal mucosa", "Benign Neoplasm of Buccal Mucosa", "benign neoplasm of buccal mucosa", "benign tumor of the buccal mucosa", "Benign Tumor of the Buccal Mucosa", "Benign Neoplasm of the Buccal Mucosa", "benign neoplasm of the buccal mucosa", "Benign neoplasm of buccal mucosa (disorder)", "benign neoplasm of buccal mucosa (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of buccal mucosa", "shortest_name_length": 26}
{"curie": "UMLS:C5238802", "names": ["Fatty acid oxidation disorder", "Myopathy Secondary to Fatty Acid Oxidation Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myopathy Secondary to Fatty Acid Oxidation Disorder", "shortest_name_length": 29}
{"curie": "OMIM:609535", "names": ["Proguanil, Poor Metabolism of", "PROGUANIL, POOR METABOLISM OF", "OMEPRAZOLE, POOR METABOLISM OF", "MEPHENYTOIN, POOR METABOLISM OF", "CLOPIDOGREL, POOR METABOLISM OF", "DRUG METABOLISM, POOR, CYP2C19-RELATED", "Drug Metabolism, Poor, CYP2C19-Related", "CLOPIDOGREL, POOR METABOLISM OF (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 29}
{"curie": "MONDO:0012938", "names": ["DBA7", "DIAMOND-BLACKFAN ANEMIA 7", "Diamond-Blackfan Anemia 7", "Diamond-Blackfan anemia 7", "RPL11 Diamond-Blackfan anemia", "Diamond-Blackfan Anemia type 7", "RPL11-related Diamond-Blackfan anemia", "Diamond-Blackfan anemia caused by mutation in RPL11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diamond-Blackfan anemia 7", "shortest_name_length": 4}
{"curie": "MONDO:0032862", "names": ["HYDCC1", "hydrocephalus, congenital communicating, 1", "HYDROCEPHALUS, CONGENITAL COMMUNICATING, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hydrocephalus, congenital communicating, 1", "shortest_name_length": 6}
{"curie": "UMLS:C3272825", "names": ["Colorectal High Grade B-Cell Lymphoma, Not Otherwise Specified", "Colorectal B-Cell Lymphoma, Unclassifiable, with Features Intermediate between Diffuse Large B-Cell Lymphoma and Burkitt Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal High Grade B-Cell Lymphoma, Not Otherwise Specified", "shortest_name_length": 62}
{"curie": "MONDO:0009914", "names": ["PDD", "Pseudodiastrophic dwarfism", "Pseudodiastrophic dysplasia", "pseudodiastrophic dysplasia", "PSEUDODIASTROPHIC DYSPLASIA", "Pseudodiastrophic dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudodiastrophic dysplasia", "shortest_name_length": 3}
{"curie": "UMLS:C2316460", "names": ["pseudobulbar affect", "Pseudobulbar affect", "Pseudobulbar affect (finding)", "pseudobulbar affect (diagnosis)", "Pathological laughing and crying"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pseudobulbar affect", "shortest_name_length": 19}
{"curie": "UMLS:C5208248", "names": ["Immune-mediated hypothyroidism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immune-mediated hypothyroidism", "shortest_name_length": 30}
{"curie": "UMLS:C3897980", "names": ["Pathological Gynecomastia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathological Gynecomastia", "shortest_name_length": 25}
{"curie": "MONDO:0011331", "names": ["Congenital chylothorax", "congenital chylothorax", "Congenital Chylothorax", "chylothorax, congenital", "Chylothorax, congenital", "CHYLOTHORAX, CONGENITAL", "Hydrothorax, Congenital", "HYDROTHORAX, CONGENITAL", "hydrothorax, congenital", "Congenital chylothorax (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital chylothorax", "shortest_name_length": 22}
{"curie": "UMLS:C4331400", "names": ["Temporal Lobe and Parietal Lobe Ependymal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Temporal Lobe and Parietal Lobe Ependymal Tumor", "shortest_name_length": 47}
{"curie": "MONDO:0005610", "names": ["Urov disease", "Kaschin-Beck", "Kashin-Bek disease", "Kashin Beck Disease", "Kaschin-Bek disease", "Kashin-Beck disease", "Kashin-Beck Disease", "Disease, Kashin-Beck", "Kaschin-Beck disease", "Endemic polyarthritis", "Osteoarthritis deformans", "Osteoarthrosis deformans", "Kashin-Beck disease (disorder)", "Kashin-Beck disease (diagnosis)", "Kaschin-Beck disease, unspecified site", "Kaschin-Beck disease, site unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kashin-Beck disease", "shortest_name_length": 12}
{"curie": "UMLS:C0302255", "names": ["Simple Lentigo", "simplex lentigo", "lentigo simplex", "Lentigo simplex", "Lentigo Simplex", "Lentigo simplex (disorder)", "lentigo simplex (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lentigo simplex", "shortest_name_length": 14}
{"curie": "UMLS:C4553252", "names": ["Stage IIA Ovarian Cancer", "Stage IIA Ovarian Cancer AJCC v8", "Stage IIA Ovarian Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Ovarian Cancer AJCC v8", "shortest_name_length": 24}
{"curie": "UMLS:C4054540", "names": ["Infection-associated membranous nephropathy", "Membranous Nephropathy - Infection Associated", "Membranous glomerulonephritis co-occurrent with infectious disease", "Membranous glomerulonephritis co-occurrent with infectious disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infection-associated membranous nephropathy", "shortest_name_length": 43}
{"curie": "UMLS:C3897068", "names": ["Childhood Pineocytic Tumor", "Childhood Pineocytic Neoplasm", "Pineal Parenchymal Cell Neoplasm", "Childhood Pineal Parenchymal Cell Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Pineal Parenchymal Cell Neoplasm", "shortest_name_length": 26}
{"curie": "MONDO:0017500", "names": ["tibiofibular terminal transverse meromelia, unilateral", "congenital absence of both lower leg and foot, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital absence of both lower leg and foot, unilateral", "shortest_name_length": 54}
{"curie": "MONDO:0020010", "names": ["nervous system infection", "infections nervous system", "Infection of nervous system", "nervous system infectious disease", "diseases infectious nervous system", "nervous system infectious disorder", "Nervous System Infectious Disorder", "Infectious disease of nervous system", "Infectious disease of the nervous system", "infectious disorder of the nervous system", "Infectious disease of nervous system (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infectious disorder of the nervous system", "shortest_name_length": 24}
{"curie": "UMLS:C3146257", "names": ["Stage II Colon Cancer", "Stage II Colon Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Colon Cancer AJCC v7", "shortest_name_length": 21}
{"curie": "MONDO:0020216", "names": ["secondary congenital glaucoma", "secondary dysgenetic glaucoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary dysgenetic glaucoma", "shortest_name_length": 29}
{"curie": "UMLS:C4528618", "names": ["Stage IB Vulvar Cancer", "Stage IB Vulvar Cancer AJCC v8", "Stage IB Vulvar Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Vulvar Cancer AJCC v8", "shortest_name_length": 22}
{"curie": "UMLS:C2346462", "names": ["Idiopathic Right Bundle Branch Block", "Idiopathic Right Bundle Branch Block by EKG Finding", "Idiopathic Right Bundle Branch Block by ECG Finding"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Idiopathic Right Bundle Branch Block by ECG Finding", "shortest_name_length": 36}
{"curie": "UMLS:C4763542", "names": ["Unresectable Skin Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Skin Carcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C1262109", "names": ["Procedural hypotension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Procedural hypotension", "shortest_name_length": 22}
{"curie": "UMLS:C1335460", "names": ["Stage IV Hepatoblastoma", "Postsurgical Stage IV Hepatoblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postsurgical Stage IV Hepatoblastoma", "shortest_name_length": 23}
{"curie": "UMLS:C0340515", "names": ["heart dysfunction", "Dysfunction;heart", "dysfunction heart", "dysfunction; heart", "Myocardial depression", "myocardial dysfunction", "Myocardial dysfunction", "dysfunction; myocardial", "Myocardial dysfunction (disorder)", "myocardial dysfunction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myocardial dysfunction", "shortest_name_length": 17}
{"curie": "MONDO:0000937", "names": ["Treponema encephalitis", "syphilitic encephalitis", "Syphilitic encephalitis", "neurosyphilitic encephalitis", "Treponema caused encephalitis", "Syphilitic encephalitis (disorder)", "syphilitic encephalitis (diagnosis)", "neurosyphilitic encephalitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syphilitic encephalitis", "shortest_name_length": 22}
{"curie": "MONDO:0017059", "names": ["neural tube closure defect", "neural tube closure disease", "disorder of neural tube closure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neural tube closure defect", "shortest_name_length": 26}
{"curie": "MONDO:0800036", "names": ["MTTC MELAS syndrome", "MELAS syndrome caused by mutation in MTTC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MELAS syndrome caused by mutation in MTTC", "shortest_name_length": 19}
{"curie": "MONDO:0003972", "names": ["gastric body cancer", "Gastric Body Cancer", "cancer of gastric body", "Cancer of Gastric Body", "gastric body carcinoma", "Gastric Body Carcinoma", "Cancer of Body of Stomach", "Carcinoma of Gastric Body", "cancer of body of stomach", "body of stomach carcinoma", "carcinoma of gastric body", "Cancer of the Gastric Body", "cancer of the gastric body", "Carcinoma of body of stomach", "carcinoma of body of stomach", "Carcinoma of Body of Stomach", "gastric body (stomach) cancer", "carcinoma of the gastric body", "Carcinoma of the Gastric Body", "Gastric Body (Stomach) Cancer", "gastric malignant carcinoma body", "cancer of the body of the stomach", "Cancer of the Body of the Stomach", "Carcinoma of the Body of the Stomach", "carcinoma of the body of the stomach", "Carcinoma of body of stomach (disorder)", "Carcinoma of body of stomach (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric body carcinoma", "shortest_name_length": 19}
{"curie": "UMLS:C5418989", "names": ["Recurrent Hairy Cell Leukemia Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Hairy Cell Leukemia Variant", "shortest_name_length": 37}
{"curie": "MONDO:0021656", "names": ["NSGCT", "nonseminomatous germinoma", "Nonseminomatous germ cell tumor", "nonseminomatous germ cell tumor", "non-seminomatous germ cell tumor", "Nongerminomatous Germ Cell Tumor", "NONSEMINOMATOUS GERM CELL TUMORS", "nongerminomatous germ cell tumor", "Non-seminomatous Germ Cell Tumor", "Nongerminomatous germ cell tumor", "Germ cell tumor, nonseminomatous", "Non-seminomatous germ-cell tumors", "Non-germinomatous Germ Cell Tumor", "Germ cell tumour, nonseminomatous", "non-germinomatous germ cell tumor", "non-dysgerminomatous germ cell tumor", "Non-dysgerminomatous Germ Cell Tumor", "nonseminomatous germinoma (diagnosis)", "NSGCT Nonseminomatous germ cell tumor", "Germ cell tumor, nonseminomatous (morphologic abnormality)", "Nongerminomatous Germ Cell Tumor Including Central Nervous System", "Nongerminomatous germ cell tumor Including central nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nongerminomatous germ cell tumor", "shortest_name_length": 5}
{"curie": "MONDO:0008382", "names": ["Autosomal dominant retinoschisis", "Retinoschisis autosomal dominant", "autosomal dominant retinoschisis", "retinoschisis autosomal dominant", "retinoschisis, autosomal dominant", "Retinoschisis, Autosomal Dominant", "RETINOSCHISIS, AUTOSOMAL DOMINANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinoschisis, autosomal dominant", "shortest_name_length": 32}
{"curie": "UMLS:C0155822", "names": ["Woakes", "Woakes' syndrome", "Woakes' ethmoiditis", "ethmoiditis; Woakes", "Woakes; ethmoiditis", "Sinus polyp degeneration", "Polypoid sinus degeneration", "Polypoid Sinus Degeneration", "polypoid sinus degeneration", "degeneration; sinus, polypoid", "sinus; degeneration, polypoid", "Woakes' ethmoiditis (disorder)", "Woakes' ethmoiditis (diagnosis)", "Woakes' syndrome or ethmoiditis", "Polypoid sinus degeneration (disorder)", "polypoid sinus degeneration (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Polypoid sinus degeneration", "shortest_name_length": 6}
{"curie": "MONDO:0005121", "names": ["Enterococcus faecalis infection", "Enterococcus faecalis infectious disease", "Enterococcus faecalis disease or disorder", "Enterococcus faecalis caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Enterococcus faecalis infection", "shortest_name_length": 31}
{"curie": "MONDO:0001420", "names": ["cranial nerve V tumors", "Cranial Nerve V Tumors", "Trigeminal Nerve Tumor", "trigeminal nerve tumor", "trigeminal nerve tumors", "Tumors, Cranial Nerve V", "Trigeminal Nerve Tumors", "tumors, cranial nerve V", "tumor of Trigeminal nerve", "Tumor of Trigeminal Nerve", "Trigeminal Nerve Neoplasm", "trigeminal nerve neoplasm", "cranial nerve V neoplasms", "tumor of trigeminal nerve", "fifth cranial nerve tumor", "Cranial Nerve V Neoplasms", "Fifth Cranial Nerve Tumor", "neoplasms, cranial nerve V", "trigeminal nerve neoplasms", "Trigeminal Nerve Neoplasms", "Neoplasms, Cranial Nerve V", "Neoplasm of trigeminal nerve", "Tumor of Fifth Cranial Nerve", "neoplasm of trigeminal nerve", "Neoplasm of Trigeminal Nerve", "tumor of fifth cranial nerve", "Fifth Cranial Nerve Neoplasm", "fifth cranial nerve neoplasm", "Tumor of the Trigeminal Nerve", "tumor of the trigeminal nerve", "neoplasm of fifth cranial nerve", "Neoplasm of Fifth Cranial Nerve", "tumor of the fifth cranial nerve", "Neoplasm of the Trigeminal Nerve", "neoplasm of the trigeminal nerve", "Tumor of the Fifth Cranial Nerve", "Neoplasm of the Fifth Cranial Nerve", "trigeminal nerve neoplasm (disease)", "neoplasm of the fifth cranial nerve", "Neoplasm of trigeminal nerve (disorder)", "neoplasm of fifth cranial nerve (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trigeminal nerve neoplasm", "shortest_name_length": 22}
{"curie": "MONDO:0011835", "names": ["EPM5", "SANDO", "PME type 5", "EPM5, FORMERLY", "epilepsy, progressive myoclonic, 5", "spinocerebellar ataxia with epilepsy", "progressive myoclonus epilepsy type 5", "epilepsy, progressive myoclonic, type 5", "PRICKLE2 progressive myoclonic epilepsy", "EPILEPSY, PROGRESSIVE MYOCLONIC, 5, FORMERLY", "epilepsy, progressive myoclonic, 5, formerly", "SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS", "sensory ataxic neuropathy, dysarthria, and ophthalmoparesis", "Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis", "progressive myoclonic epilepsy caused by mutation in PRICKLE2", "Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome", "sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome", "EPILEPSY, PROGRESSIVE MYOCLONIC, WITH SENSORY ATAXIC NEUROPATHY", "epilepsy, progressive myoclonic, with sensory ataxic neuropathy", "mitochondrial recessive ataxia syndrome (includes SANDO and SCAE)", "SANDO (sensory ataxic neuropathy dysarthria ophthalmoparesis) syndrome", "Sensory ataxic neuropathy with dysarthria and ophthalmoparesis syndrome", "autosomal recessive sensory ataxic neuropathy with mitochondrial DNA deletions", "SENSORY ATAXIC NEUROPATHY WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE", "sensory ataxic neuropathy with mitochondrial DNA deletions, autosomal recessive", "Sensory ataxic neuropathy with dysarthria and ophthalmoparesis syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sensory ataxic neuropathy, dysarthria, and ophthalmoparesis", "shortest_name_length": 4}
{"curie": "UMLS:C4525623", "names": ["Stage III Ampulla of Vater Neuroendocrine Tumor", "Stage III Ampulla of Vater Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Ampulla of Vater Neuroendocrine Tumor AJCC v8", "shortest_name_length": 47}
{"curie": "UMLS:C0004161", "names": ["Injury;sports", "Sports Injury", "sports injury", "Sports injury", "Injury, Sports", "sports injuries", "athletic injury", "Sports injuries", "Athletic Injury", "Sports Injuries", "athletics injury", "Injury, Athletic", "Injuries, Sports", "Athletic Injuries", "athletic injuries", "Sports injury, NOS", "athletics injuries", "Injuries, Athletic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Athletic Injuries", "shortest_name_length": 13}
{"curie": "EFO:1000789", "names": ["osteoarthritis, hand"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteoarthritis, hand", "shortest_name_length": 20}
{"curie": "UMLS:C0751671", "names": ["Type IV Machado-Joseph Disease", "Type IV Machado Joseph Disease", "Machado-Joseph Disease Type IV", "Machado Joseph Disease Type IV"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Machado-Joseph Disease Type IV", "shortest_name_length": 30}
{"curie": "UMLS:C0393444", "names": ["Meningitis chemical", "chemical meningitis", "Chemical meningitis", "MENINGITIS CHEMICAL", "Chemical meningitis (disorder)", "chemical meningitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chemical meningitis", "shortest_name_length": 19}
{"curie": "UMLS:C0345999", "names": ["Multiple pigmented terminal hair cysts", "Multiple Pigmented Terminal Hair Cysts", "Multiple pigmented terminal hair cysts (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Multiple pigmented terminal hair cysts", "shortest_name_length": 38}
{"curie": "MONDO:0021072", "names": ["Chromaffinoma", "chromaffin tumor", "Chromaffin Tumor", "Chromaffin tumor", "Chromaffin Neoplasm", "chromaffin neoplasm", "Familial pheochromocytoma", "Islet cell tumor syndrome", "Sympathetic paraganglioma", "Sympathetic Paraganglioma", "sympathetic paraganglioma", "Familial islet cell tumors", "Sympathetic Paraganglionic Neoplasm", "sympathetic Paraganglionic neoplasm", "sympathetic nervous system paraganglioma", "paraganglioma of sympathetic nervous system", "Sympathetic paraganglioma (morphologic abnormality)", "Bilateral pheochromocytoma and islet cell adenoma of the pancreas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sympathetic paraganglioma", "shortest_name_length": 13}
{"curie": "UMLS:C4725076", "names": ["Advanced Urothelial Cancer", "Advanced Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Urothelial Carcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0000231", "names": ["Far Eastern spotted fever", "Far Eastern Spotted Fever", "Far eastern spotted fever", "Far eastern spotted fever (disorder)", "Rickettsia heilongjiangensis spotted fever"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Far eastern spotted fever", "shortest_name_length": 25}
{"curie": "MONDO:0020075", "names": ["genetic isolated obesity", "monogenic isolated obesity", "genetic non-syndromic obesity", "monogenic obesity due to a leptin-melanocortin pathway anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genetic non-syndromic obesity", "shortest_name_length": 24}
{"curie": "MONDO:0007851", "names": ["KTCN1", "keratoconus 1", "Keratoconus 1", "KERATOCONUS 1", "keratoconus type 1", "VSX1 keratoconus (disease)", "keratoconus (disease) caused by mutation in VSX1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratoconus 1", "shortest_name_length": 5}
{"curie": "MONDO:0014016", "names": ["SPG49", "HSAN9", "SPG49, FORMERLY", "hereditary spastic paraplegia 49", "TECPR2 hereditary spastic paraplegia", "hereditary spastic paraplegia type 49", "autosomal recessive spastic paraplegia 49", "spastic paraplegia 49, autosomal recessive", "autosomal recessive spastic paraplegia type 49", "SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE, FORMERLY", "hereditary spastic paraplegia caused by mutation in TECPR2", "neuropathy, hereditary sensory and autonomic, type IX, with developmental delay", "NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IX, WITH DEVELOPMENTAL DELAY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 49", "shortest_name_length": 5}
{"curie": "UMLS:C4524314", "names": ["Stage IIB Uterine Sarcoma", "Stage IIB Uterine Sarcoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Uterine Sarcoma AJCC v7", "shortest_name_length": 25}
{"curie": "UMLS:C0855162", "names": ["Stage III Extragonadal Mixed Germ Cell Tumor", "Stage III Extragonadal Primary Mixed Germ Cell Tumor", "Stage III Extragonadal Primary Germ Cell Tumor Mixed", "Extragonadal primary germ cell tumor mixed stage III", "Extragonadal primary germ cell tumour mixed stage III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extragonadal primary germ cell tumor mixed stage III", "shortest_name_length": 44}
{"curie": "UMLS:C4076057", "names": ["Urinary tract infection caused by Klebsiella", "Urinary tract infection caused by Klebsiella (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urinary tract infection caused by Klebsiella", "shortest_name_length": 44}
{"curie": "MONDO:0035173", "names": ["9q21.13 microdeletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "9q21.13 microdeletion syndrome", "shortest_name_length": 30}
{"curie": "MONDO:0000530", "names": ["Rectal Adenoma", "rectal adenoma", "Rectal adenoma", "rectum adenoma", "Adenoma of rectum", "adenoma of rectum", "Adenoma of Rectum", "Adenoma of the Rectum", "adenoma of the rectum", "Adenoma of rectum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rectum adenoma", "shortest_name_length": 14}
{"curie": "MONDO:0023273", "names": ["bednar tumor", "Bednar Tumor", "Bednar tumor", "Tumor, Bednar", "Bednars Tumor", "Bednar tumour", "Bednar's Tumor", "Pigmented DFSP", "Pigmented DFSPs", "Tumor, Bednar's", "DFSP, Pigmented", "DFSPs, Pigmented", "Pigmented dermatofibrosarcoma", "Pigmented storiform neurofibroma", "Pigmented Dermatofibrosarcoma Protuberan", "Pigmented Dermatofibrosarcoma Protuberans", "pigmented dermatofibrosarcoma protuberans", "Protuberan, Pigmented Dermatofibrosarcoma", "Dermatofibrosarcoma Protuberan, Pigmented", "Pigmented dermatofibrosarcoma protuberans", "Protuberans, Pigmented Dermatofibrosarcoma", "Dermatofibrosarcoma Protuberans, Pigmented", "protuberans; dermatofibrosarcoma, pigmented", "dermatofibrosarcoma; protuberans, pigmented", "pigmented dermatofibrosarcoma protuberans of skin", "Pigmented dermatofibrosarcoma protuberans of skin", "pigmented dermatofibrosarcoma protuberans (bednar tumor)", "Pigmented Dermatofibrosarcoma Protuberans (Bednar Tumor)", "Pigmented dermatofibrosarcoma protuberans of skin (disorder)", "pigmented dermatofibrosarcoma protuberans of skin (diagnosis)", "Pigmented dermatofibrosarcoma protuberans (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pigmented dermatofibrosarcoma protuberans", "shortest_name_length": 12}
{"curie": "MONDO:0013700", "names": ["PNLIPD", "PL DEFICIENCY", "PL deficiency", "Isolated lipase deficiency", "pancreatic lipase deficiency", "PANCREATIC LIPASE DEFICIENCY", "Pancreatic Lipase Deficiency", "pancreatic colipase deficiency", "LIPASE AND COLIPASE, DEFICIENCY OF", "lipase and colipase, deficiency of", "Congenital pancreatic lipase deficiency", "Congenital absence of pancreatic lipase", "LIPASE, CONGENITAL ABSENCE OF PANCREATIC", "lipase, congenital absence of pancreatic", "Pancreatic triglyceride lipase deficiency", "pancreatic triglyceride lipase deficiency", "COLIPASE, CONGENITAL ABSENCE OF PANCREATIC", "Congenital deficiency of pancreatic lipase", "colipase, congenital absence of pancreatic", "Pancreatic triacylglycerol lipase deficiency", "pancreatic triacylglycerol lipase deficiency", "lipase and colipase, congenital absence of pancreatic", "LIPASE AND COLIPASE, CONGENITAL ABSENCE OF PANCREATIC", "Pancreatic triacylglycerol lipase deficiency (disorder)", "pancreatic triacylglycerol lipase deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic triacylglycerol lipase deficiency", "shortest_name_length": 6}
{"curie": "UMLS:C4682467", "names": ["Cervical Cancer by AJCC v8 Stage", "Cervical Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Cancer by AJCC v8 Stage", "shortest_name_length": 32}
{"curie": "MONDO:0033014", "names": ["EKVP4", "erythrokeratodermia variabilis et progressiva 4", "erythrokeratodermia variabilis ET progressiva 4", "ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythrokeratodermia variabilis et progressiva 4", "shortest_name_length": 5}
{"curie": "UMLS:C0751642", "names": ["Anterior frontopolar epilepsy", "Anterior Fronto-Polar Epilepsy", "Epilepsy, Anterior Fronto Polar", "Epilepsy, Anterior Fronto-Polar", "Anterior Fronto-Polar Epilepsies", "Epilepsies, Anterior Fronto-Polar", "Anterior frontopolar epilepsy (disorder)", "Anterior frontopolar epilepsy (diagnosis)", "frontal lobe epilepsy anterior frontopolar"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epilepsy, Anterior Fronto-Polar", "shortest_name_length": 29}
{"curie": "MONDO:0016969", "names": ["trisomy 19q", "Trisomy 19q", "19q trisomy", "19q+ syndrome", "Duplication 19q", "19q duplication", "dup(19q) syndrome", "partial trisomy 19q", "chromosome 19q trisomy", "19q duplication syndrome", "duplication 19q syndrome", "Chromosome 19, trisomy 19q", "chromosome 19q duplication", "partial trisomy of chromosome 19q", "chromosome 19q duplication syndrome", "partial duplication of chromosome 19q", "partial trisomy of the long arm of chromosome 19", "partial duplication of the long arm of chromosome 19", "partial duplication of the long arm of chromosome type 19"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of the long arm of chromosome 19", "shortest_name_length": 11}
{"curie": "MONDO:0000813", "names": ["cardiac tuberculosis", "Cardiovascular Tuberculosis", "Cardiovascular Tuberculoses", "cardiovascular tuberculosis", "Tuberculosis, Cardiovascular", "Tuberculoses, Cardiovascular"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiac tuberculosis", "shortest_name_length": 20}
{"curie": "UMLS:C5420154", "names": ["Advanced Anal Canal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Anal Canal Squamous Cell Carcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0002885", "names": ["Erythrasma", "erythrasma", "ERYTHRASMA", "cutaneous erythrasma", "Erythrasma (disorder)", "cutaneous erythrasma (diagnosis)", "infection due to Corynebacterium minutissimum", "Infection due to Corynebacterium minutissimum", "Infection caused by Corynebacterium minutissimum", "Infection caused by Corynebacterium minutissimum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythrasma", "shortest_name_length": 10}
{"curie": "MONDO:0019873", "names": ["Trisomy 4pter", "trisomy 4pter", "distal trisomy 4p", "Distal trisomy 4p", "Distal duplication 4p", "distal duplication 4p", "Telomeric duplication 4p", "telomeric duplication 4p", "4p16.3 microduplication syndrome", "4p16.3 microduplication syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "4p16.3 microduplication syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0030866", "names": ["NEDCASB", "NEURODEVELOPMENTAL DISORDER WITH CARDIOMYOPATHY, SPASTICITY, AND BRAIN ABNORMALITIES", "neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities", "shortest_name_length": 7}
{"curie": "MONDO:0012621", "names": ["DIS", "dis", "Deafness-infertility syndrome", "Deafness-Infertility Syndrome", "Deafness infertility syndrome", "DEAFNESS-INFERTILITY SYNDROME", "deafness-infertility syndrome", "deafness and male infertility", "Hearing loss-infertility syndrome", "CHROMOSOME 15q15.3 DELETION SYNDROME", "Chromosome 15q15.3 Deletion Syndrome", "chromosome 15Q15.3 deletion syndrome", "Chromosome 15q15.3 deletion syndrome", "sensorineural deafness and male infertility", "Sensorineural deafness and male infertility", "Sensorineural Deafness and Male Infertility", "deafness, sensorineural, and Male infertility", "Deafness, Sensorineural, And Male Infertility", "DEAFNESS, SENSORINEURAL, AND MALE INFERTILITY", "Sensorineural deafness and male infertility (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness-infertility syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0010496", "names": ["MRX12", "MRX35", "XLID12", "X-linked mental retardation 35", "X-linked mental retardation 12", "MENTAL RETARDATION, X-LINKED 12", "mental retardation, X-linked 35", "MENTAL RETARDATION, X-LINKED 35", "mental retardation, X-linked 12", "intellectual disability, X-linked 35", "intellectual disability, X-linked 12", "mental retardation, X-linked type 12", "intellectual disability, X-linked type 12", "X-linked mental retardation 35 (MRX35, XLMR35)", "X-linked mental retardation 12 (MRX12, XLMR12)", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 12", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 35", "X-linked intellectual disability-short stature-overweight syndrome", "intellectual developmental disorder, X-linked 12, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability-short stature-overweight syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0007109", "names": ["CDA 3", "CDAN3", "CDAN3A", "CDA III", "CDA type 3", "CDA type III", "CDA, TYPE III", "CDA, TYPE IIIA", "hereditary benign erythroreticulosis", "ERYTHRORETICULOSIS, HEREDITARY BENIGN", "Erythroreticulosis, hereditary benign", "Erythroreticulosis, Hereditary Benign", "Anemia With Multinucleated Erythroblasts", "ANEMIA WITH MULTINUCLEATED ERYTHROBLASTS", "anemia with multinucleated erythroblasts", "anaemia with multinucleated erythroblasts", "Congenital dyserythropoietic anemia type 3", "congenital dyserythropoietic anemia type 3", "dyserythropoietic anemia, congenital type 3", "Congenital dyserythropoietic anaemia type 3", "congenital dyserythropoietic anemia type III", "dyserythropoietic Anemia, congenital, type 3", "Congenital dyserythropoietic anemia type III", "Congenital Dyserythropoietic Anemia, Type III", "congenital dyserythropoietic anaemia type III", "Congenital dyserythropoietic anaemia type III", "Congenital dyserythropoietic anemia, type III", "anemia, congenital dyserythropoietic, type III", "dyserythropoietic anemia, congenital, type III", "Anemia, Dyserythropoietic Congenital, Type III", "Dyserythropoietic Anemia, Congenital, Type III", "Congenital dyserythropoietic anaemia, type III", "ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE III", "ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IIIa", "ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IIIA", "DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE IIIA", "Anemia, Dyserythropoietic, Congenital, Type III", "Congenital dyserythropoietic anemia, type III (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital dyserythropoietic anemia type 3", "shortest_name_length": 5}
{"curie": "UMLS:C0334609", "names": ["Angioblastic Meningioma", "Angioblastic meningioma", "angioblastic; meningioma", "Angioblastic Meningiomas", "meningioma; angioblastic", "Meningioma, Angioblastic", "Meningiomas, Angioblastic", "Hemangioblastic meningioma", "Hemangioblastic Meningioma", "hemangioblastic; meningioma", "Haemangioblastic meningioma", "meningioma; hemangioblastic", "Meningioma, Hemangioblastic", "Hemangioblastic Meningiomas", "Meningiomas, Hemangioblastic", "Hemangioblastic meningioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemangioblastic Meningioma", "shortest_name_length": 23}
{"curie": "UMLS:C5237034", "names": ["Solid Pseudopapillary Tumor of the Ovary", "Primary Ovarian Solid Pseudopapillary Tumor", "Solid Pseudopapillary Neoplasm of the Ovary", "Primary Ovarian Solid Pseudopapillary Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Solid Pseudopapillary Neoplasm of the Ovary", "shortest_name_length": 40}
{"curie": "MONDO:0044304", "names": ["HPANBH4", "Mild Non-BH4-Deficient Hyperphenylalaninemia", "hyperphenylalaninemia, mild, non-BH4-deficient", "HYPERPHENYLALANINEMIA, MILD, NON-BH4-DEFICIENT", "hyperphenylalaninemia due to DNAJC12 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperphenylalaninemia due to DNAJC12 deficiency", "shortest_name_length": 7}
{"curie": "MONDO:0003371", "names": ["Breast Leiomyosarcoma", "breast leiomyosarcoma", "Leiomyosarcoma of Breast", "leiomyosarcoma of breast", "leiomyosarcoma of the breast", "Leiomyosarcoma of the Breast", "breast myosarcoma leiomyosarcoma", "leiomyosarcoma of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast leiomyosarcoma", "shortest_name_length": 21}
{"curie": "MONDO:0000390", "names": ["BMD", "VMD2", "BVMD", "Best", "Best disease", "Best Disease", "Disease, Best", "Best's disease", "Best's Disease", "best's disease", "Disease, Best's", "vitelliform dystrophy", "Vitelliform Dystrophy", "Vitelliform dystrophy", "BEST MACULAR DYSTROPHY", "Best macular dystrophy", "Best Macular Dystrophy", "Macular Dystrophy, Best", "Dystrophy, Best Macular", "Best's disease (diagnosis)", "Vitelliform macular lesions", "Vitelliform Macular Dystrophy", "vitelliform macular dystrophy", "Vitelliform macular dystrophy", "macular dystrophy, vitelliform", "Dystrophy, Vitelliform Macular", "Macular Dystrophy, Vitelliform", "Vitelliform Macular Dystrophies", "Macular Dystrophies, Vitelliform", "Dystrophies, Vitelliform Macular", "Vitelliform-like macular lesions", "Vitelliform dystrophy (disorder)", "vitelliform dystrophy (diagnosis)", "MACULAR DYSTROPHY, VITELLIFORM, 2", "Best Vitelliform Macular Dystrophy", "Best vitelliform macular dystrophy", "Vitelliform macular dystrophy type 2", "Early-onset vitelliform macular dystrophy", "Polymorphic vitelline macular degeneration", "MACULAR DEGENERATION, POLYMORPHIC VITELLINE", "Macular Degeneration, Polymorphic Vitelline", "juvenile-onset vitelliform macular dystrophy", "Juvenile-onset vitelliform macular dystrophy", "Best vitelliform macular dystrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitelliform macular dystrophy", "shortest_name_length": 3}
{"curie": "UMLS:C3468050", "names": ["Adult Malignant Meningioma", "adult malignant meningioma", "malignant meningioma, adult", "adult anaplastic meningioma", "Adult Anaplastic Meningioma", "meningioma, adult malignant", "anaplastic meningioma, adult", "Anaplastic (Malignant) Meningioma", "Adult Anaplastic (Malignant) Meningioma", "adult anaplastic (malignant) meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Anaplastic (Malignant) Meningioma", "shortest_name_length": 26}
{"curie": "MONDO:0000363", "names": ["gummatous syphilis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gummatous syphilis", "shortest_name_length": 18}
{"curie": "MONDO:0043892", "names": ["Device related infection", "device related infection", "Prosthesis related infection", "Prosthesis Related Infection", "prosthesis-related infection", "Prosthesis-Related Infection", "Prosthesis-Related Infections", "Infection, Prosthesis Related", "Prosthesis Related Infections", "Related Infection, Prosthesis", "prosthesis related infections", "Related Infections, Prosthesis", "Infections, Prosthesis-Related", "infections, prosthesis-related", "prosthesis-related infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prosthesis-related infectious disease", "shortest_name_length": 24}
{"curie": "UMLS:C3264002", "names": ["Juvenile Myoclonic Epilepsy, Intractable, without Status Epilepticus", "Juvenile myoclonic epilepsy, intractable, without status epilepticus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Juvenile Myoclonic Epilepsy, Intractable, without Status Epilepticus", "shortest_name_length": 68}
{"curie": "MONDO:0100413", "names": ["AML, biCEBPA", "AML, CEBPA Biallelic Mutation", "AML, CEBP Biallelic Gene Mutation", "AML, CEBPA Biallelic Gene Mutation", "AML, biallelic CEBPA gene mutation", "AML with biallelic mutations of CEBPA", "AML, C/EBPalpha Biallelic Gene Mutation", "AML, C/EBP-Alpha Biallelic Gene Mutation", "acute myeloid leukemia, biallelic CEBPA gene mutation", "acute myeloid leukemia with biallelic mutation of CEBPA", "Acute Myeloid Leukemia with Biallelic Mutations of CEBPA", "AML, CCAAT Enhancer Binding Protein Alpha Biallelic Gene Mutation", "AML, CCAAT/Enhancer Binding Protein Alpha Biallelic Gene Mutation", "AML, CCAAT/Enhancer Binding Protein, Alpha Biallelic Gene Mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, biallelic CEBPA gene mutation", "shortest_name_length": 12}
{"curie": "MONDO:0021679", "names": ["Gram-Positive Bacterial Infection", "Gram-positive bacterial infection", "infection, Gram-positive bacterial", "Gram Positive Bacterial Infections", "Gram-Positive Bacterial Infections", "Gram Positive bacterial infections", "gram-positive bacterial infections", "Bacterial Infection, Gram-Positive", "Infection, Gram-Positive Bacterial", "Gram-positive bacterial infections", "bacterial infection, Gram-positive", "Infections, Gram Positive Bacterial", "bacterial infections, Gram Positive", "infections, Gram Positive bacterial", "Bacterial Infections, Gram Positive", "Bacterial Infections, Gram-Positive", "Infections, Gram-Positive Bacterial", "bacterial infections, Gram-positive", "infections, Gram-positive bacterial", "Disease due to Gram-positive bacteria", "Disease caused by Gram-positive bacteria", "Gram-positive bacterial infection (diagnosis)", "Disease caused by Gram-positive bacteria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gram-positive bacterial infections", "shortest_name_length": 33}
{"curie": "MONDO:0008569", "names": ["GTHR", "GRTH", "Gthr", "GRTHD", "thyroid hormone resistance", "thyroid hormone unresponsiveness", "THYROID HORMONE UNRESPONSIVENESS", "Thyroid Hormone Resistance, Generalized, Autosomal Dominant", "thyroid hormone resistance, generalized, autosomal dominant", "THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL DOMINANT", "hyperthyroxinemia, familial euthyroid, secondary to pituitary and peripheral resistance to thyroid hormones", "HYPERTHYROXINEMIA, FAMILIAL EUTHYROID, SECONDARY TO PITUITARY AND PERIPHERAL RESISTANCE TO THYROID HORMONES", "Hyperthyroxinemia, Familial Euthyroid, Secondary To Pituitary And Peripheral Resistance To Thyroid Hormones"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid hormone resistance, generalized, autosomal dominant", "shortest_name_length": 4}
{"curie": "MONDO:0000698", "names": ["gamma-amino butyric acid metabolism disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gamma-amino butyric acid metabolism disorder", "shortest_name_length": 44}
{"curie": "MONDO:0006036", "names": ["GRCT", "Granulosa cell tumor", "granulosa cell tumor", "cell granulosa tumor", "Granulosa Cell Tumor", "tumor cell granulosa", "Granulosa cell tumour", "cells granulosa tumor", "granulosa cell tumour", "granulosa cell; tumor", "Granulosa Cell Cancer", "tumor; granulosa cell", "Granulosa Cell Tumors", "Tumor, Granulosa Cell", "granulosa cell tumors", "Granulosa cell cancer", "Granulosa Cells Cancer", "Cell Cancer, Granulosa", "Cancer, Granulosa Cell", "Granulosa Cell Cancers", "Tumors, Granulosa Cell", "Cell Cancers, Granulosa", "Granulosa Cells Cancers", "tumor of granulosa cell", "Granulosa Cell Neoplasm", "Granulosa cell neoplasm", "Cancers, Granulosa Cell", "granulosa cell neoplasm", "Cells Cancer, Granulosa", "Granulosa cell tumor NOS", "Granulosa cell carcinoma", "Cells Cancers, Granulosa", "Granulosa cell tumor, NOS", "Granulosa cell tumour NOS", "Cancer of Granulosa Cells", "granulosa cell; carcinoma", "carcinoma; granulosa cell", "Granulosa cell tumour, NOS", "neoplasm of granulosa cell", "Granulosa cell malignant tumor", "Malignant granulosa cell tumor", "Malignant Granulosa Cell Tumor", "Malignant granulosa cell tumour", "Granulosa cell tumor, malignant", "GRANULOSA CELL TUMOR, MALIGNANT", "granulosa cell tumor, adult type", "granulosa cell; tumor, malignant", "Granulosa cell tumour, malignant", "Granulosa cell tumor, adult type", "tumor; granulosa cell, malignant", "malignant granulosa cell neoplasm", "granulosa cell neoplasm (disease)", "Malignant Granulosa Cell Neoplasm", "Granulosa cell tumor, sarcomatoid", "granulosa cell tumor, undetermined", "granulosa cell tumour, sarcomatoid", "Granulosa cell tumour, sarcomatoid", "Malignant adult granulosa cell tumor", "Malignant adult granulosa cell tumour", "Maligant granulosa cell tumor of the ovary", "Granulosa cell tumor (morphologic abnormality)", "Granulosa cell tumor, malignant (morphologic abnormality)", "granulosa cell tumor, adult type (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "granulosa cell tumor", "shortest_name_length": 4}
{"curie": "MONDO:0032778", "names": ["AMCM", "AMC3", "arthrogryposis multiplex congenita-3", "ARTHROGRYPOSIS MULTIPLEX CONGENITA, MYOGENIC TYPE", "arthrogryposis multiplex congenita, myogenic type", "arthrogryposis multiplex congenita 3, myogenic type", "ARTHROGRYPOSIS MULTIPLEX CONGENITA 3, MYOGENIC TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis multiplex congenita 3, myogenic type", "shortest_name_length": 4}
{"curie": "MONDO:0007439", "names": ["DEOXYRIBOSE-5-PHOSPHATE ALDOLASE DEFICIENCY", "deoxyribose-5-phosphate aldolase deficiency", "Deoxyribose-5-Phosphate Aldolase Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deoxyribose-5-phosphate aldolase deficiency", "shortest_name_length": 43}
{"curie": "MONDO:0007127", "names": ["DISH", "dish", "Forestier", "Forestier Disease", "forestier disease", "Forestier disease", "Forestiers Disease", "Disease, Forestier", "Forestier's Disease", "forestier's disease", "Forestier's disease", "Disease, Forestier's", "Ankylosing hyperostosis", "Forestier-Rotes Disease", "Forestier Rotes Disease", "Disease, Forestier-Rotes", "Forestier-Rotes-Querol syndrome", "Ankylosing vertebral hyperostosis", "ankylosing hyperostosis vertebral", "Vertebral Ankylosing Hyperostoses", "ankylosing vertebral hyperostosis", "Vertebral Ankylosing Hyperostosis", "Hyperostoses, Vertebral Ankylosing", "Ankylosing Hyperostosis, Vertebral", "Ankylosing Hyperostoses, Vertebral", "Hyperostosis, Vertebral Ankylosing", "Forestier and Rotes-Querol syndrome", "Ankylosing hyperostosis [Forestier]", "diffuse idiopathic skeletal hyperostosis", "Diffuse idiopathic skeletal hyperostosis", "Senile ankylosing vertebral hyperostosis", "DIFFUSE IDIOPATHIC SKELETAL HYPEROSTOSIS", "Diffuse Idiopathic Skeletal Hyperostosis", "Hyperostosis, Diffuse Idiopathic Skeletal", "Disseminated idiopathic skeletal hyperostosis", "disseminated idiopathic skeletal hyperostosis", "ankylosing vertebral hyperostosis (diagnosis)", "Ankylosing vertebral hyperostosis with tylosis", "ANKYLOSING VERTEBRAL HYPEROSTOSIS WITH TYLOSIS", "Ankylosing Vertebral Hyperostosis with Tylosis", "ankylosing vertebral hyperostosis with tylosis", "DISH - Diffuse idiopathic skeletal hyperostosis", "diffuse idiopathic skeletal hyperostosis (DISH)", "Diffuse idiopathic skeletal hyperostosis [DISH]", "DISH (diffuse idiopathic skeletal hyperostosis)", "Disseminated idiopathic skeletal hyperostosis (disorder)", "diffuse idiopathic skeletal hyperostosis (DISH) (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diffuse idiopathic skeletal hyperostosis", "shortest_name_length": 4}
{"curie": "UMLS:C4743656", "names": ["Recurrent Metastatic Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Metastatic Malignant Neoplasm", "shortest_name_length": 39}
{"curie": "MONDO:0003296", "names": ["Cellular Leiomyoma", "Cellular leiomyoma", "cellular leiomyoma", "Cellular leiomyoma (morphologic abnormality)", "cellular leiomyoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cellular leiomyoma", "shortest_name_length": 18}
{"curie": "MONDO:0014266", "names": ["ARMD15", "age related macular degeneration 15", "C9 age-related macular degeneration", "macular degeneration, age-related, 15", "MACULAR DEGENERATION, AGE-RELATED, 15", "age related macular degeneration type 15", "macular degeneration, age-related, type 15", "macular degeneration, age-related, 15, susceptibility to", "age-related macular degeneration caused by mutation in C9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "age related macular degeneration 15", "shortest_name_length": 6}
{"curie": "MONDO:0016421", "names": ["Toxic oil syndrome", "toxic oil syndrome", "Spanish toxic oil syndrome", "Toxic oil syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "toxic oil syndrome", "shortest_name_length": 18}
{"curie": "MONDO:0006025", "names": ["hereditary trait", "Trait, hereditary", "hereditary traits", "Hereditary disorder, trait", "autosomal recessive disease", "disease, autosomal recessive", "Hereditary disorder trait, NOS", "Hereditary disorder, recessive", "Recessive hereditary disorder, NOS", "Hereditary disorder trait (autosomal)", "autosomal recessive inherited disease", "autosomal recessive inherited disorder", "autosomal recessive hereditary disease", "autosomal recessive disease or disorder", "Autosomal recessive hereditary disorder", "autosomal recessive hereditary disorder", "disease or disorder, autosomal recessive", "recessive hereditary disorder (autosomal)", "Recessive hereditary disorder (autosomal)", "inherited genetic conditions autosomal recessive", "Autosomal recessive hereditary disorder (disorder)", "autosomal recessive hereditary disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive disease", "shortest_name_length": 16}
{"curie": "MONDO:0035238", "names": ["vegetative pyoderma gangrenosum", "Granulomatous pyoderma gangrenosum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vegetative pyoderma gangrenosum", "shortest_name_length": 31}
{"curie": "UMLS:C5556791", "names": ["Metastatic Vaginal Adenosquamous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Vaginal Adenosquamous Carcinoma", "shortest_name_length": 42}
{"curie": "UMLS:C2200348", "names": ["Renal Rhabdomyosarcoma", "Kidney Rhabdomyosarcoma", "rhabdomyosarcoma of kidney", "rhabdomyosarcoma of kidney (diagnosis)", "renal neoplasm malignant rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rhabdomyosarcoma of kidney", "shortest_name_length": 22}
{"curie": "UMLS:C0334358", "names": ["Papillary Serous Cystadenoma", "Papillary serous cystadenoma", "Papillary serous cystadenoma NOS", "Papillary serous cystadenoma, NOS", "papillary; cystadenoma, serous, unspecified site", "serous; cystadenoma, papillary, unspecified site", "cystadenoma; serous, papillary, unspecified site", "cystadenoma; papillary, serous, unspecified site", "Papillary serous cystadenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Papillary serous cystadenoma", "shortest_name_length": 28}
{"curie": "MONDO:0019232", "names": ["disorder of peptide metabolism", "inborn disorder of peptide metabolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of peptide metabolism", "shortest_name_length": 30}
{"curie": "MONDO:0013845", "names": ["ARCND2", "Auriculocondylar syndrome 2", "AURICULOCONDYLAR SYNDROME 2", "auriculocondylar syndrome 2", "AURICULOCONDYLAR syndrome 2", "PLCB4 auriculocondylar syndrome", "Auriculocondylar syndrome type 2", "auriculocondylar syndrome caused by mutation in PLCB4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "auriculocondylar syndrome 2", "shortest_name_length": 6}
{"curie": "UMLS:C1332999", "names": ["Childhood Primary Cutaneous Anaplastic Large Cell Lymphoma", "Pediatric Primary Cutaneous Anaplastic Large Cell Lymphoma", "Pediatric Primary Cutaneous K-1+ Anaplastic Large Cell Lymphoma", "Childhood Primary Cutaneous Ki-1+ Anaplastic Large Cell Lymphoma", "Childhood Primary Cutaneous CD30+ Anaplastic Large Cell Lymphoma", "Pediatric Primary Cutaneous CD30+ Anaplastic Large Cell Lymphoma", "Childhood Primary Cutaneous CD30-Positive Anaplastic Large Cell Lymphoma", "Childhood Primary Cutaneous Ki-1 Positive Anaplastic Large Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Primary Cutaneous Anaplastic Large Cell Lymphoma", "shortest_name_length": 58}
{"curie": "UMLS:C2698204", "names": ["Metastatic Lobular Breast Carcinoma", "Metastatic Breast Lobular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Breast Lobular Carcinoma", "shortest_name_length": 35}
{"curie": "MONDO:0013998", "names": ["CRPT2", "CARPENTER SYNDROME 2", "CARPENTER syndrome 2", "Carpenter syndrome 2", "MEGF8 Carpenter syndrome", "Carpenter syndrome type 2", "MEGF8-related Carpenter syndrome", "Carpenter syndrome caused by mutation in MEGF8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MEGF8-related Carpenter syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C1335048", "names": ["Non-Neoplastic Tracheal Disease", "Non-Neoplastic Tracheal Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Tracheal Disorder", "shortest_name_length": 31}
{"curie": "MONDO:0007701", "names": ["PFHB2", "PFHBII", "progressive familial heart block type 2", "heart block progressive familial type 2", "progressive familial heart block type II", "PROGRESSIVE FAMILIAL HEART BLOCK, TYPE II", "Progressive Familial Heart Block, Type II", "Progressive familial heart block, type II", "progressive familial heart block, type II", "Progressive familial heart block, type II (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive familial heart block type II", "shortest_name_length": 5}
{"curie": "MONDO:0014723", "names": ["YUHAL", "dup(17)(p11.2p12)", "Dup(17)(p11.2p12)", "trisomy 17p11.2p12", "Trisomy 17p11.2p12", "trisomy 17p11.2-p12", "Trisomy 17p11.2-p12", "Yuan-Harel-Lupski syndrome", "YUAN-Harel-Lupski syndrome", "Yuan Harel Lupski syndrome", "YUAN-HAREL-LUPSKI SYNDROME", "17p11.2p12 microduplication syndrome", "PMP22-RAI1 contiguous gene duplication syndrome", "Peripheral myelin protein 22-retinoic acid induced 1 contiguous gene duplication syndrome", "Peripheral myelin protein 22-retinoic acid induced 1 contiguous gene duplication syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PMP22-RAI1 contiguous gene duplication syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0012984", "names": ["PHARC", "PHARC syndrome", "Peripheral neuropathy Fiskerstrand type", "peripheral neuropathy, Fiskerstrand type", "Peripheral neuropathy, Fiskerstrand type", "Polyneuropathy-deafness-ataxia-retinitis pigmentosa-cataract syndrome", "POLYNEUROPATHY, HEARING LOSS, ATAXIA, RETINITIS PIGMENTOSA, AND CATARACT", "polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract", "polyneyropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract", "Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract", "Polyneuropathy-hearing loss-ataxia-retinitis pigmentosa-cataract syndrome", "polyneuropathy-hearing loss-ataxia-retinitis pigmentosa-cataract syndrome", "Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome", "PHARC (polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract) syndrome", "Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PHARC syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0004765", "names": ["ASTHMA INTRINSIC", "Intrinsic asthma", "asthma intrinsic", "intrinsic asthma", "intrinsic; asthma", "asthma; intrinsic", "non-atopic asthma", "asthma nonallergic", "nonallergic asthma", "Nonallergic asthma", "asthma non-allergic", "asthma; nonallergic", "nonallergic; asthma", "Non-allergic asthma", "intrinsic asthma (diagnosis)", "intrinsic nonallergic asthma", "Non-allergic asthma (disorder)", "asthma; intrinsic, nonallergic", "intrinsic; asthma, nonallergic", "Non-allergic asthma (diagnosis)", "Asthma due to internal immunological process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intrinsic asthma", "shortest_name_length": 16}
{"curie": "UMLS:C0085396", "names": ["Neisseriaceae Infection", "Neisseriaceae Infections", "Infection, Neisseriaceae", "Infections, Neisseriaceae"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neisseriaceae Infections", "shortest_name_length": 23}
{"curie": "MONDO:0018902", "names": ["HCA", "LIAD", "LIVER ADENOMA", "liver adenoma", "ADENOMA LIVER", "Adenoma liver", "adenoma liver", "Liver adenomas", "adenomas liver", "Hepatic adenoma", "Benign Hepatoma", "Adenoma;hepatic", "Benign hepatoma", "hepatic adenoma", "adenomas hepatic", "benign; hepatoma", "Hepatoma, Benign", "Benign Hepatomas", "hepatoma; benign", "Hepatoma, benign", "Adenoma of liver", "Hepatomas, Benign", "Liver cell adenoma", "liver cell adenoma", "LIVER CELL ADENOMA", "Liver Cell Adenoma", "adenoma; liver cell", "Liver Cell Adenomas", "liver cell; adenoma", "Adenoma, Liver Cell", "Adenomas, Liver Cell", "HEPATOCELLULAR ADENOMA", "Hepatocellular Adenoma", "Hepatocellular adenoma", "Adenoma of Liver Cells", "hepatocellular adenoma", "adenoma of liver cells", "benign adenoma of liver", "Hepatocellular Adenomas", "Adenoma, Hepatocellular", "hepatocellular; adenoma", "hepatocellular adenomas", "adenoma; hepatocellular", "Adenomas, Hepatocellular", "HEPATOCELLULAR ADENOMA <S>", "adenoma of the liver cells", "Adenoma of the Liver Cells", "Adenoma of liver (disorder)", "HCA - Hepatocellular adenoma", "ADENOMA, HEPATOCELLULAR, BENIGN", "adenoma, hepatocellular, benign", "Hepatocellular adenoma (disorder)", "benign adenoma of liver (diagnosis)", "Liver cell adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatocellular adenoma", "shortest_name_length": 3}
{"curie": "MONDO:0015824", "names": ["OBLFC1", "Oblique facial clefts", "oblique facial clefts", "FACIAL CLEFTING, OBLIQUE, 1", "Oculomaxillofacial dysostosis", "oculomaxillofacial dysostosis", "Richieri Costa Gorlin syndrome", "Richieri-Costa-Gorlin syndrome", "Oculomaxillofacial dysostosis (disorder)", "oculomaxillofacial dysostosis (diagnosis)", "Oculomaxillofacial dysplasia with oblique facial clefts", "oculomaxillofacial dysplasia with oblique facial clefts", "OCULOMAXILLOFACIAL DYSPLASIA WITH OBLIQUE FACIAL CLEFTS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculomaxillofacial dysostosis", "shortest_name_length": 6}
{"curie": "UMLS:C1336067", "names": ["Splenic Manifestation of LGL", "Splenic Manifestation of T-Cell Large Granular Lymphocyte Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Splenic Manifestation of T-Cell Large Granular Lymphocyte Leukemia", "shortest_name_length": 28}
{"curie": "MONDO:0012012", "names": ["CMTDIC", "Di-Cmtc", "DI-CMTC", "YARS Charcot-Marie-Tooth disease", "Charcot-Marie-Tooth disease dominant intermediate C", "Charcot-Marie-Tooth Disease, Dominant Intermediate C", "CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE C", "Charcot-Marie-Tooth disease, dominant intermediate C", "Charcot-Marie-Tooth neuropathy dominant intermediate C", "Charcot-Marie-Tooth disease caused by mutation in YARS", "CHARCOT-MARIE-TOOTH NEUROPATHY, DOMINANT INTERMEDIATE C", "Charcot-Marie-Tooth neuropathy, dominant Intermediate C", "Charcot-Marie-Tooth Neuropathy, Dominant Intermediate C", "YARS-related intermediate Charcot-Marie-Tooth neuropathy", "Charcot-Marie-Tooth disease dominant intermediate type C", "Charcot-Marie-Tooth disease, dominant Intermediate type C", "autosomal dominant intermediate Charcot-Marie-Tooth disease type C", "Charcot-Marie-Tooth disease autosomal dominant intermediate type C", "Autosomal dominant intermediate Charcot-Marie-Tooth disease type C", "Autosomal dominant intermediate Charcot-Marie-Tooth disease type C (disorder)", "Autosomal dominant intermediate Charcot-Marie-Tooth disease type C (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease dominant intermediate C", "shortest_name_length": 6}
{"curie": "MONDO:0023538", "names": ["Kaplowitz-Bodurtha syndrome", "Kaplowitz Bodurtha syndrome", "Hypopituitarism microphthalmia", "hypopituitarism microphthalmia", "congenital hypopituitarism and microphthalmia", "Congenital hypopituitarism and microphthalmia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kaplowitz-Bodurtha syndrome", "shortest_name_length": 27}
{"curie": "UMLS:C0855145", "names": ["Stage IV Nodal Marginal Zone Lymphoma", "Nodal marginal zone B-cell lymphoma stage IV", "Stage IV Nodal Marginal Zone B-Cell Lymphoma", "Nodal Marginal Zone B-Cell Lymphoma Stage IV", "Ann Arbor Stage IV Nodal Marginal Zone Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nodal marginal zone B-cell lymphoma stage IV", "shortest_name_length": 37}
{"curie": "UMLS:C1336132", "names": ["stage IB endometrial cancer", "stage IB endometrial carcinoma", "stage IB uterine corpus cancer", "Stage IB Uterine Corpus Cancer", "Stage IB Uterine Corpus Cancer AJCC v7", "stage IB uterine corpus cancer AJCC v7", "Stage IB Uterine (including Endometrial) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Uterine Corpus Cancer AJCC v7", "shortest_name_length": 27}
{"curie": "UMLS:C3274519", "names": ["Surfactant Protein C Deficiency", "Surfactant Apoprotein C Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Surfactant Protein C Deficiency", "shortest_name_length": 31}
{"curie": "UMLS:C5670677", "names": ["Stage IIA1 Cervical Cancer FIGO 2009", "Stage IIA1 Cervical Carcinoma FIGO 2009"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA1 Cervical Cancer FIGO 2009", "shortest_name_length": 36}
{"curie": "UMLS:C0349368", "names": ["Adrenal hypertension", "adrenal hypertension", "Hypertension, adrenal", "Endocrine Hypertension", "hypertension endocrine", "Endocrine hypertension", "endocrine hypertension", "endocrinal hypertension", "disorder endocrine hypertension", "endocrine; disorder hypertension", "hypertension; endocrine disorders", "Hypertension secondary to endocrine disorder", "secondary hypertension to endocrine disorders", "hypertension secondary to endocrine disorders", "Hypertension secondary to endocrine disorders", "hypertension; secondary, due to endocrine disorders", "secondary; hypertension, due to endocrine disorders", "Hypertension secondary to endocrine disorder (disorder)", "hypertension secondary to endocrine disorders (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypertension secondary to endocrine disorder", "shortest_name_length": 20}
{"curie": "UMLS:C3146260", "names": ["Stage I Hypopharyngeal Carcinoma", "Stage I Hypopharyngeal Throat Cancer", "Stage I Hypopharyngeal Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Hypopharyngeal Carcinoma AJCC v7", "shortest_name_length": 32}
{"curie": "MONDO:0018777", "names": ["autosomal dominant preaxial polydactyly-upperback hypertrichosis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant preaxial polydactyly-upperback hypertrichosis syndrome", "shortest_name_length": 73}
{"curie": "UMLS:C0854495", "names": ["Hepatitis F"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatitis F", "shortest_name_length": 11}
{"curie": "MONDO:0021645", "names": ["esophageal varix bleeding", "bleeding esophageal varix", "ESOPHAGEAL VARIX BLEEDING", "bleeding esophageal varice", "Bleeding esophageal varices", "esophageal varices bleeding", "bleeding esophageal varices", "Esophageal varices ruptured", "Bleeding oesophageal varices", "varices; esophagus, bleeding", "hemorrhage; esophagus, varix", "Oesophageal varices ruptured", "esophagus; varix, hemorrhage", "esophagus; hemorrhage, varix", "Esophageal Varices Hemorrhage", "esophageal varices hemorrhage", "Esophageal varices hemorrhage", "ESOPHAGEAL VARIX WITH BLEEDING", "haemorrhage oesophageal varices", "Oesophageal varices haemorrhage", "Esophageal varices with bleeding", "esophageal varices with bleeding", "BOV - Bleeding esophageal varices", "Oesophageal varices with bleeding", "Esophageal varices with hemorrhage", "BOV - Bleeding oesophageal varices", "esophageal varices with hemorrhage", "Oesophageal varices with haemorrhage", "Bleeding esophageal varices (disorder)", "esophageal varices with hemorrhage (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophageal varices with bleeding", "shortest_name_length": 25}
{"curie": "MONDO:0004411", "names": ["duodenal gastrinoma", "Duodenal Gastrinoma", "Gastrinoma of duodenum", "Gastrinoma of Duodenum", "gastrinoma of duodenum", "Gastrinoma of the Duodenum", "gastrinoma of the duodenum", "malignant duodenal gastrinoma", "Duodenal Gastrin-Producing NET", "duodenal gastrin-producing NET", "Gastrinoma of duodenum (disorder)", "Gastrin Producing Tumor of Duodenum", "gastrin producing tumor of duodenum", "duodenal G-cell gastrin producing tumor", "gastrin producing tumor of the duodenum", "Duodenal G-Cell Gastrin Producing Tumor", "Gastrin Producing Tumor of the Duodenum", "duodenal gastrin-producing neuroendocrine tumor", "Duodenal Gastrin-Producing Neuroendocrine Tumor", "duodenum gastrin-producing neuroendocrine tumor", "gastrin-producing neuroendocrine tumor of duodenum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "duodenal gastrin-producing neuroendocrine tumor", "shortest_name_length": 19}
{"curie": "MONDO:0005501", "names": ["CDGII", "CDG II", "MOGS-CDG", "MGAT2-CDG", "B4GALT1-CDG", "MOGS-CDG (CDG-2b)", "MGAT2-CDG (CDG-2a)", "B4GALT1-CDG (CDG-2d)", "congenital disorder of glycosylation type II", "Congenital disorder of glycosylation type II", "Congenital Disorder Of Glycosylation, Type II", "congenital disorders of glycosylation, type II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital disorder of glycosylation type II", "shortest_name_length": 5}
{"curie": "MONDO:0001431", "names": ["Optic Neuropathy", "Optic neuropathy", "Damaged optic nerve", "Optic neuropathy NOS", "Hereditary optic neuropathy", "nutritional optic neuropathy", "Nutritional optic neuropathy", "toxic or nutritional optic neuropathy", "nutritional optic neuropathy (diagnosis)", "Disorder of optic nerve due to nutritional deficiency", "Disorder of optic nerve due to nutritional deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "toxic or nutritional optic neuropathy", "shortest_name_length": 16}
{"curie": "UMLS:C0262576", "names": ["Nerve palsy", "nerve palsy", "NERVE PALSY", "nerve palsies", "nerve paralysis", "Nerve paralysis", "Nerve Paralysis", "NERVE PARALYSIS", "nerve; paralysis", "paralysis; nerve", "Nerve palsy (disorder)", "nerve palsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nerve palsy", "shortest_name_length": 11}
{"curie": "UMLS:C0475590", "names": ["grade 2 intraventricular hemorrhage neonatal", "grade 2 intraventricular hemorrhage, neonatal", "grade II neonatal intraventricular hemorrhage", "grade II intraventricular hemorrhage neonatal", "Intraventricular Hemorrhage of Newborn Grade 2", "Grade 2 Intraventricular Hemorrhage of the Newborn", "grade II neonatal intraventricular hemorrhage (diagnosis)", "Intraventricular (nontraumatic) hemorrhage, grade 2, of newborn", "Grade 2 Intraventricular (Nontraumatic) Hemorrhage of Fetus and Newborn", "Intraventricular Hemorrhage of the Newborn without Ventricular Dilatation", "Intraventricular (Nontraumatic) Hemorrhage, Grade 2, of Fetus and Newborn", "Intraventricular (nontraumatic) hemorrhage, grade 2, of fetus and newborn", "Intraventricular (nontraumatic) haemorrhage, grade 2, of fetus and newborn", "Intraventricular (nontraumatic) haemorrhage, grade 2, of foetus and newborn", "Intraventricular (nontraumatic) hemorrhage, grade 2, of fetus and newborn (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade 2 Intraventricular Hemorrhage of the Newborn", "shortest_name_length": 44}
{"curie": "MONDO:0010342", "names": ["AUTSX3", "autism susceptibility, X-linked 3", "susceptibility to X-linked autism 3", "AUTISM, SUSCEPTIBILITY TO, X-LINKED 3", "autism, susceptibility to, X-linked 3", "autism, susceptibility to, X-linked type 3", "AUTISM, X-LINKED, SUSCEPTIBILITY TO, 3 (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autism, susceptibility to, X-linked 3", "shortest_name_length": 6}
{"curie": "UMLS:C3273049", "names": ["Bile Duct Intraductal Papillary Neoplasm, Low Grade", "Bile Duct Intraductal Papillary Neoplasm, Low-Grade", "Bile Duct IPN with Low Grade Intraepithelial Neoplasia", "Bile Duct Papillary Neoplasm with Low Grade Intraepithelial Neoplasia", "Intraductal papillary neoplasm with low-grade intraepithelial neoplasia", "Intraductal papillary neoplasm with low grade intraepithelial neoplasia", "Intraductal Papillary Neoplasm with Low Grade Intraepithelial Neoplasia", "Bile Duct Intraductal Papillary Neoplasm with Low Grade Intraepithelial Neoplasia", "Intraductal papillary neoplasm with low-grade intraepithelial neoplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraductal papillary neoplasm with low-grade intraepithelial neoplasia", "shortest_name_length": 51}
{"curie": "MONDO:0002444", "names": ["MELANCHOLIA", "Melancholia", "melancholia", "Melancholias", "Melancholia NOS", "Melancholia, NOS", "Melancholic depression", "Melancholic Depression", "melancholic depression", "depression melancholic", "Depression with Melancholic Features", "depression with melancholic features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melancholia", "shortest_name_length": 11}
{"curie": "UMLS:C5555430", "names": ["B-Cell Lymphoproliferative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-Cell Lymphoproliferative Disorder", "shortest_name_length": 35}
{"curie": "MONDO:0010226", "names": ["DSS", "SRXY2", "46,XY SEX REVERSAL 2", "46,XY sex reversal 2", "46,XY SEX reversal 2", "46,XY Sex reversal type 2", "dosage-sensitive Sex reversal", "DOSAGE-SENSITIVE SEX REVERSAL", "dosage-sensitive sex reversal", "Dosage-sensitive sex reversal", "46,XY Sex reversal, Dax1-related", "46,XY sex reversal, DAX1-related", "46,XY SEX REVERSAL, DAX1-RELATED", "46XY sex reversal 2, dosage-sensitive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XY sex reversal 2", "shortest_name_length": 3}
{"curie": "MONDO:0008789", "names": ["ANEMIA, NONSPHEROCYTIC HEMOLYTIC, ASSOCIATED WITH ABNORMALITY OF RED CELL MEMBRANE", "Anemia, Nonspherocytic Hemolytic, associated with Abnormality of Red Cell Membrane", "anemia, nonspherocytic hemolytic, associated with abnormality of red cell membrane"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anemia, nonspherocytic hemolytic, associated with abnormality of red cell membrane", "shortest_name_length": 82}
{"curie": "MONDO:0013947", "names": ["DSMA5", "dSMA5", "young adult-onset dHMN", "Young adult-onset dHMN", "distal spinal muscular atrophy type 5", "Young adult-onset distal hereditary motor neuropathy", "young adult-onset distal hereditary motor neuropathy", "spinal muscular atrophy, distal, autosomal recessive, 5", "SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 5", "autosomal recessive distal spinal muscular atrophy type 5", "Autosomal recessive distal spinal muscular atrophy type 5", "spinal muscular atrophy, distal, autosomal recessive, type 5", "Young adult-onset distal hereditary motor neuropathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "young adult-onset distal hereditary motor neuropathy", "shortest_name_length": 5}
{"curie": "UMLS:C4745057", "names": ["BCR Prostate Carcinoma", "Micro-Metastatic Prostate Carcinoma", "PSA-Only Recurrent Prostate Carcinoma", "Biochemically Recurrent Prostate Carcinoma", "PSA-Only (Biochemically) Recurrent Prostate Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Biochemically Recurrent Prostate Carcinoma", "shortest_name_length": 22}
{"curie": "MONDO:0008541", "names": ["Testis torsion", "Torsion;testis", "torsion testis", "testis torsion", "TORSION TESTIS", "torsion testes", "torsion; testis", "testicle torsion", "TESTICLE TORSION", "Torsion of testis", "Torsion of Testis", "testicle; torsion", "torsion of testis", "testicles torsion", "Testicular Torsion", "testicular Torsion", "Testicular torsion", "testicular torsion", "TESTICULAR TORSION", "Torsion, Testicular", "Testicular Torsions", "torsion of testicle", "Torsion of testicle", "Torsions, Testicular", "testicle cord torsion", "torsion of the testis", "spermatic cord torsion", "Spermatic Cord Torsion", "SPERMATIC CORD TORSION", "Spermatic cord torsion", "cord spermatic torsion", "torsion; spermatic cord", "spermatic cord; torsion", "SPERMATIC CORD, TORSION", "Torsion, Spermatic Cord", "Spermatic Cord Torsions", "Torsions, Spermatic Cord", "Torsion of spermatic cord", "torsion of testicular cord", "Torsion Of Testicular Cord", "TORSION OF TESTICULAR CORD", "Torsion of testis (disorder)", "torsion of testis (diagnosis)", "Torsion of spermatic cord NOS", "Torsion of testis, unspecified", "spermatic cord torsion (diagnosis)", "Torsion of spermatic cord (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatic cord torsion", "shortest_name_length": 14}
{"curie": "MONDO:0002934", "names": ["intravascular angiomyoma", "Intravascular Angiomyoma", "Intravascular Angioleiomyoma", "intravascular angioleiomyoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intravascular angioleiomyoma", "shortest_name_length": 24}
{"curie": "MONDO:0010520", "names": ["ATS", "ATS1", "Alport syndrome X-linked", "X-Linked Alport Syndrome", "X-linked Alport syndrome", "Alport syndrome, X-linked", "Alport Syndrome, X-Linked", "Alport Syndrome, X Linked", "ALPORT SYNDROME 1, X-LINKED", "hemorrhagic familial nephritis", "congenital hereditary hematuria", "hemorrhagic hereditary nephritis", "NEPHROPATHY AND DEAFNESS, X-LINKED", "nephropathy and deafness, X-linked", "Alport syndrome X-linked (disorder)", "Alport syndrome X-linked (diagnosis)", "Alport syndrome 1, X-linked, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked Alport syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C0495107", "names": ["VIN 2", "VIN 3", "Grade 3 VIN", "Vulvar HSIL", "Grade 2 VIN", "VIN Grade 2", "Grade II VIN", "VIN, Usual Type", "VIN 2 of Usual Type", "VIN 3 of Usual Type", "Vulvar Bowen Disease", "Vulvar Bowenoid Dysplasia", "Moderate vulvar dysplasia", "dysplasia; vulva, moderate", "Moderate dysplasia of vulva", "moderate dysplasia of vulva", "Vulvar Severe Squamous Dysplasia", "Vulvar Moderate Squamous Dysplasia", "Vulva Intraepithelial Neoplasia Grade 2", "moderate dysplasia of vulva (diagnosis)", "Vulva Intraepithelial Neoplasia Grade 3", "Grade 2 Vulvar Intraepithelial Neoplasia", "Vulval intraepithelial neoplasia grade 2", "Vulvar Intraepithelial Neoplasia Grade 2", "Vulvar Intraepithelial Neoplasia Grade 3", "vulvar intraepithelial neoplasia grade II", "Grade II Vulvar Intraepithelial Neoplasia", "Vulval intraepithelial neoplasia grade II", "vulva; intraepithelial neoplasia, grade II", "Intraepithelial Neoplasia of Vulva Grade 2", "neoplasia; intraepithelial, vulva, grade II", "Vulvar Intraepithelial Neoplasia, Usual Type", "Vulvar intraepithelial neoplasia II [VIN II]", "Intraepithelial Neoplasia of the Vulva Grade 2", "VIN - Vulval intraepithelial neoplasia grade 2", "Vulvar intraepithelial neoplasia [VIN], grade II", "Vulvar Intraepithelial Neoplasia 3 of Usual Type", "Vulvar Intraepithelial Neoplasia 2 of Usual Type", "Vulvar High Grade Squamous Intraepithelial Lesion", "Vulvar High-Grade Squamous Intraepithelial Lesion", "High Grade Vulvar Squamous Intraepithelial Lesion", "Vulval intraepithelial neoplasia grade 2 (disorder)", "vulvar squamous cell intraepithelial neoplasia, grade II", "squamous cell intraepithelial neoplasia of vulva, grade II", "squamous cell intraepithelial neoplasia of vulva, grade II (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulval intraepithelial neoplasia grade 2", "shortest_name_length": 5}
{"curie": "MONDO:0011788", "names": ["Cloverleaf skull-multiple congenital anomalies syndrome", "cloverleaf skull-multiple congenital anomalies syndrome", "Multiple Congenital Anomalies Syndrome with Cloverleaf Skull", "multiple congenital anomalies syndrome with cloverleaf skull", "Cloverleaf skull with multiple congenital anomalies syndrome", "MULTIPLE CONGENITAL ANOMALIES SYNDROME WITH CLOVERLEAF SKULL", "Cloverleaf skull with multiple congenital anomalies syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cloverleaf skull-multiple congenital anomalies syndrome", "shortest_name_length": 55}
{"curie": "UMLS:C4744416", "names": ["Metastatic Malignant Pancreatic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Malignant Pancreatic Neoplasm", "shortest_name_length": 40}
{"curie": "MONDO:0033486", "names": ["HLD14", "hypomyelinating leukodystrophy 14", "leukodystrophy, hypomyelinating, 14", "LEUKODYSTROPHY, HYPOMYELINATING, 14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukodystrophy, hypomyelinating, 14", "shortest_name_length": 5}
{"curie": "UMLS:C0242380", "names": ["Libman-Sacks disease", "LIBMAN-SACKS DISEASE", "Libman-Sacks Disease", "Libman Sacks Disease", "Disease, Libman-Sacks", "Libman-Sacks (etiology)", "Sacks-Libman (etiology)", "libman-sacks endocarditis", "Libman-Sacks endocarditis", "libman sacks endocarditis", "LIBMAN SACKS ENDOCARDITIS", "Endocarditis, Libman-Sachs", "Libman-Sacks (manifestation)", "Sacks-Libman (manifestation)", "Atypical verrucal endocarditis", "Atypical verrucous endocarditis", "ENDOCARDITIS, ATYPICAL, VERRUCOUS", "Nonbacterial verrucal endocardiosis", "Nonbacterial verrucous endocarditis", "nonbacterial verrucal endocardiosis", "Libman-Sacks; endocarditis (etiology)", "ENDOCARDITIS, NONBACTERIAL, VERRUCOUS", "endocarditis; Libman-Sacks (etiology)", "Libman-Sacks; endocarditis (manifestation)", "endocarditis; Libman-Sacks (manifestation)", "Nonbacterial verrucal endocardiosis (disorder)", "nonbacterial verrucal endocardiosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Libman-Sacks Disease", "shortest_name_length": 20}
{"curie": "MONDO:0003659", "names": ["lymphoma", "Lymphoma", "childhood lymphoma", "pediatric lymphoma", "Pediatric Lymphoma", "Childhood Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pediatric lymphoma", "shortest_name_length": 8}
{"curie": "MONDO:0019126", "names": ["IDI", "intractable diarrhea of infancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intractable diarrhea of infancy", "shortest_name_length": 3}
{"curie": "MONDO:0009401", "names": ["HPII", "HYRPRO2", "hyperprolinemia type 2", "type 2 hyperprolinemia", "Hyperprolinemia type 2", "Type 2 hyperprolinemia", "Hyperprolinaemia type 2", "type II hyperprolinemia", "ALDH4A1 hyperprolinemia", "Hyperprolinemia type II", "hyperprolinemia, type 2", "hyperprolinemia type II", "Hyperprolinemia, type II", "Hyperprolinemia, Type II", "hyperprolinemia, type II", "HYPERPROLINEMIA, TYPE II", "Hyperprolinaemia type II", "Hyperprolinemia type 2 (disorder)", "type II hyperprolinemia (diagnosis)", "Pyrroline-5-carboxylate reductase deficiency", "hyperprolinemia caused by mutation in ALDH4A1", "Pyrroline Carboxylate Dehydrogenase Deficiency", "Deficiency of pyrroline-5-carboxylate reductase", "Pyrroline-5-Carboxylate Dehydrogenase Deficiency", "1-pyrroline-5-carboxylate dehydrogenase deficiency", "1-Pyrroline-5-Carboxylate Dehydrogenase Deficiency", "1-PYRROLINE-5-CARBOXYLATE DEHYDROGENASE DEFICIENCY", "delta'-Pyrroline-5-carboxylate dehydrogenase deficiency", "delta1-pyrroline-5-carboxylate dehydrogenase deficiency", "1 alpha pyrroline-5-carboxylate dehydrogenase deficiency", "Delta-1-pyrroline-5-carboxylate dehydrogenase deficiency", "Deficiency of pyrroline-5-carboxylate reductase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperprolinemia type 2", "shortest_name_length": 4}
{"curie": "MONDO:0005567", "names": ["Drug Withdrawal", "Drug withdrawal", "DRUG WITHDRAWAL", "drug withdrawal", "Withdrawal;drug", "drug withdrawals", "drugs withdrawal", "Withdrawal (Drug)", "Withdrawal Syndrome", "withdrawal disorder", "SYNDROME WITHDRAWAL", "Withdrawal syndrome", "WITHDRAWAL SYNDROME", "withdrawal syndrome", "Syndrome withdrawal", "substance withdrawal", "SUBSTANCE WITHDRAWAL", "Substance withdrawal", "syndromes withdrawal", "AOD withdrawal syndrome", "Drug Withdrawal Effects", "drug withdrawal syndrome", "DRUG ABSTINENCE SYNDROME", "DRUG WITHDRAWAL SYNDROME", "Drug withdrawal syndrome", "Drug withdrawal (diagnosis)", "Substance withdrawal syndrome", "substance withdrawal syndrome", "Substance Withdrawal Syndrome", "Drug withdrawal syndrome, NOS", "substance withdrawal disorder", "Withdrawal Syndrome, Substance", "Substance Withdrawal Syndromes", "Syndrome, Substance Withdrawal", "Withdrawal Syndromes, Substance", "Syndromes, Substance Withdrawal", "Drug withdrawal syndrome or symptoms", "Drug abstinence syndrome or symptoms", "unspecified substance withdrawal drug", "Substance withdrawal syndrome (disorder)", "Alcohol or Other Drugs withdrawal syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "substance withdrawal syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0032833", "names": ["LUTO", "lower urinary tract obstruction, congenital", "LOWER URINARY TRACT OBSTRUCTION, CONGENITAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lower urinary tract obstruction, congenital", "shortest_name_length": 4}
{"curie": "MONDO:0008501", "names": ["SWS", "Sturge", "Sturge Disease", "Sturge disease", "nevoid amentia", "weber syndrome", "Weber syndrome", "syndrome webers", "webers syndrome", "Muller syndrome", "DIMITRI DISEASE", "Sturge syndrome", "Sturge Syndrome", "Jahnke syndrome", "Dimitri disease", "Lawford syndrome", "Syndrome, Sturge", "Milles' syndrome", "Schirmer syndrome", "Sturge's Syndrome", "Syndrome, Sturge's", "Kalischer syndrome", "Schirmer's syndrome", "fourth phacomatosis", "STURGE-WEBER DISEASE", "Sturge-Weber Disease", "sturge weber disease", "Dimitri-Sturge-Weber", "sturge-weber disease", "Sturge-Weber disease", "Sturge-Weber sequence", "sturge weber syndrome", "sturge-weber syndrome", "Sturge-Weber Syndrome", "Parkes Weber Syndrome", "Sturge Weber Syndrome", "STURGE-WEBER SYNDROME", "Sturge-Weber anomalad", "STURGE-WEBER syndrome", "Sturge Weber syndrome", "sturge syndrome weber", "Sturge-Weber syndrome", "Parkes-Weber Syndrome", "Syndrome, Sturge-Weber", "Weber-Dimitri syndrome", "sturges weber syndrome", "sturges syndrome weber", "Syndrome, Parkes Weber", "Syndrome, Parkes-Weber", "neuroretinoangiomatosis", "cutaneocerebral angioma", "neurocutaneous syndrome", "Neuroretinoangiomatosis", "ectoneurodermal hamartoma", "Sturge-Weber angiomatosis", "Sturge-Weber Phakomatosis", "neuroectodermal hamartoma", "Phakomatosis, Sturge-Weber", "Phakomatosis, Sturge Weber", "meningofacial angiomatosis", "PHAKOMATOSIS, STURGE-WEBER", "leptomeningeal angiomatosis", "Sturge-Weber syndrome (SWS)", "Sturge-Weber-Thoma syndrome", "Sturge-Weber-Krabbe syndrome", "Encephalofacial angiomatosis", "Encephalotrigeminal Syndrome", "Encephalotrigeminal syndrome", "encephalotrigeminal syndrome", "Sturge-Weber-Krabbe Syndrome", "encephalofacial angiomatosis", "Sturge Weber Krabbe Syndrome", "Syndrome, Sturge-Weber-Krabbe", "STURGE WEBER DIMITRI SYNDROME", "Sturge Weber Dimitri Syndrome", "Sturge-Weber-Dimitri Syndrome", "cerebrocutaneous angiomatosis", "Sturge-Weber-Dimitri syndrome", "ANGIOMATOSIS, ENCEPHALOFACIAL", "angiomatosis encephalofacialis", "Syndrome, Sturge-Weber-Dimitri", "Sturge-Kalischer-Weber Syndrome", "Sturge-Kalischer-Weber syndrome", "STURGE-KALISCHER-WEBER SYNDROME", "Encephalocutaneous angiomatosis", "Encephalofacial hemangiomatosis", "Sturge-Weber(-Dimitri) syndrome", "Sturge Kalischer Weber Syndrome", "angiomatosis meningoulofacialis", "Sturge-Weber syndrome (disorder)", "Encephalofacial haemangiomatosis", "meningo-oculofacial angiomatosis", "Sturge-Weber-Krabbe angiomatosis", "Encephalotrigeminal angiomatosis", "encephalotrigeminal angiomatosis", "Syndrome, Sturge-Kalischer-Weber", "meningeal capillary angiomatosis", "trigemino-encephalo-angiomatosis", "Sturge-Weber disease (diagnosis)", "Parkes Weber and Dimitri syndrome", "encephalofacial neuroangiomatosis", "encephalotrigeminal; angiomatosis", "ANGIOMATOSIS, ENCEPHALOTRIGEMINAL", "neuro-oculocutaneous angiomatosis", "Meningo-Oculo-Facial Angiomatosis", "Meningo Oculo Facial Angiomatosis", "angiomatosis; encephalotrigeminal", "encephalocraniofacial angiomatosis", "Angiomatosis, Meningo-Oculo-Facial", "neuroangiomatosis encephalofacialis", "Sturge-Weber syndrome, somatic, mosaic", "Encephalofacial Hemangiomatosis Syndrome", "angioma capillare et venosum calcificans", "Syndrome, Encephalofacial Hemangiomatosis", "Hemangiomatosis Syndrome, Encephalofacial", "Angiomatosis Oculoorbital-Thalamic Syndrome", "SWS type III - isolated leptomeningeal angiomas", "SWS type I - Facial and leptomeningeal angiomas", "angiomatosis-oculo-orbito-thalamo-encephalic syndrome", "Angiomatosis oculo-orbital-thalamo-encephalic syndrome", "SWS type II - Facial angioma alone, no CNS involvement", "Meningofacial Angiomatosis-Cerebral Calcification Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sturge-Weber syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0013988", "names": ["CHTD3", "CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 3", "congenital heart defects, multiple types, 3", "congenital heart defects, multiple types, with Cardiac rhythm and conduction disturbances", "CONGENITAL HEART DEFECTS, MULTIPLE TYPES, WITH CARDIAC RHYTHM AND CONDUCTION DISTURBANCES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital heart defects, multiple types, 3", "shortest_name_length": 5}
{"curie": "UMLS:C1377767", "names": ["Recurrent Malignant Nasopharyngeal Neoplasm", "Malignant nasopharyngeal neoplasm recurrent", "Malignant neoplasm of nasopharynx recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant nasopharyngeal neoplasm recurrent", "shortest_name_length": 43}
{"curie": "UMLS:C0677723", "names": ["Recurrent Indolent Non-Hodgkin Lymphoma", "recurrent indolent adult non-Hodgkin lymphoma", "Recurrent Indolent Adult Non-Hodgkin Lymphoma", "indolent, recurrent adult non-Hodgkin lymphoma", "recurrent indolent adult non-Hodgkin's lymphoma", "Recurrent Adult Indolent Non-Hodgkin's Lymphoma", "Recurrent Indolent Adult Non-Hodgkin's Lymphoma", "recurrent adult indolent non-Hodgkin's lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Indolent Adult Non-Hodgkin Lymphoma", "shortest_name_length": 39}
{"curie": "MONDO:0100176", "names": ["AP-4 deficiency syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AP-4 deficiency syndrome", "shortest_name_length": 24}
{"curie": "MONDO:0017757", "names": ["disorder of metabolite absorption and transport"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of metabolite absorption and transport", "shortest_name_length": 47}
{"curie": "MONDO:0004962", "names": ["stage II endometrioid carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stage II endometrioid carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0001597", "names": ["Submandibular Gland Disease", "submandibular gland disease", "Disease, Submandibular Gland", "Submandibular Gland Diseases", "submandibular gland disorder", "Gland Disease, Submandibular", "Gland Diseases, Submandibular", "Diseases, Submandibular Gland", "disease of submandibular gland", "disorder of submandibular gland", "submandibular gland disease or disorder", "disease or disorder of submandibular gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "submandibular gland disorder", "shortest_name_length": 27}
{"curie": "UMLS:C4553246", "names": ["stage II ureter cancer", "Stage II Ureter Cancer", "stage II ureter cancer AJCC v8", "Stage II Ureter Cancer AJCC v8", "Stage II Ureter Urothelial Carcinoma AJCC v8", "stage II ureter urothelial carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Ureter Cancer AJCC v8", "shortest_name_length": 22}
{"curie": "MONDO:0013413", "names": ["RP45", "retinitis pigmentosa 45", "RETINITIS PIGMENTOSA 45", "CNGB1 retinitis pigmentosa", "retinitis pigmentosa type 45", "retinitis pigmentosa caused by mutation in CNGB1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 45", "shortest_name_length": 4}
{"curie": "UMLS:C4744431", "names": ["Unresectable Desmoid Tumor", "Unresectable Desmoid Fibromatosis", "Unresectable Desmoid-Type Fibromatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Desmoid Fibromatosis", "shortest_name_length": 26}
{"curie": "MONDO:0012787", "names": ["SPG39", "NTEMND", "spastic paraplegia 39", "hereditary spastic paraplegia 39", "NTE related motor neuron disorder", "NTE-RELATED MOTOR NEURON DISORDER", "NTE-related motor neuron disorder", "NTE-Related Motor Neuron Disorder", "PNPLA6 hereditary spastic paraplegia", "hereditary spastic paraplegia type 39", "Spastic paraplegia due to NTE mutation", "spastic paraplegia due to NTE mutation", "autosomal recessive spastic paraplegia 39", "Spastic Paraplegia 39, Autosomal Recessive", "SPASTIC PARAPLEGIA 39, AUTOSOMAL RECESSIVE", "spastic paraplegia 39, autosomal recessive", "autosomal recessive spastic paraplegia type 39", "Autosomal recessive spastic paraplegia type 39", "familial spastic paraplegia autosomal recessive type 39", "Autosomal recessive spastic paraplegia type 39 (disorder)", "Autosomal recessive spastic paraplegia type 39 (diagnosis)", "hereditary spastic paraplegia caused by mutation in PNPLA6", "spastic paraplegia due to neuropathy target esterase mutation", "Spastic paraplegia due to neuropathy target esterase mutation", "Spastic paraplegia due to NTE (neuropathy target esterase) mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 39", "shortest_name_length": 5}
{"curie": "MONDO:0036045", "names": ["euthyroid dysprealbuminemic hyperthyroxinemia", "Euthyroid dystransthyretinemic hyperthyroxinemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "euthyroid dysprealbuminemic hyperthyroxinemia", "shortest_name_length": 45}
{"curie": "MONDO:0010334", "names": ["DDCH", "CADDS", "Contiguous ABCD1 DXS1357E deletion syndrome", "Contiguous Abcd1-Dxs1375e Deletion Syndrome", "contiguous ABCD1/Dxs1375E deletion syndrome", "CONTIGUOUS ABCD1/DXS1375E DELETION SYNDROME", "Zellweger-like contiguous gene deletion syndrome", "DEAFNESS, DYSTONIA, AND CEREBRAL HYPOMYELINATION", "deafness, dystonia, and cerebral hypomyelination", "CADDS - contiguous ABCD1 DXS1357E deletion syndrome", "Contiguous ABCD1 DXS1357E deletion syndrome (disorder)", "deafness, dystonia, and cerebral hypomyelination, X-linked recessive", "severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome", "severe motor and intellectual disabilities-sensorineural hearing loss-dystonia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0000701", "names": ["ischemic colitis", "Colitis ischemic", "Colonic ischemia", "colonic ischemia", "Ischemic Colitis", "colitis ischemic", "ISCHEMIC COLITIS", "Ischemic colitis", "ischaemic colitis", "colitis ischaemic", "Colitis ischaemic", "Colonic ischaemia", "ischemic; colitis", "Colitis, Ischemic", "Ischaemic colitis", "Colitis;ischaemic", "colitis; ischemic", "Ischemic colitis, NOS", "Ischaemic colitis, NOS", "Ischemic colitis (disorder)", "ischemic colitis (diagnosis)", "Ischemic colitis as other diagnosis for the colon", "Ischemic colitis as reason for lower g.i. examination"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ischemic colitis", "shortest_name_length": 16}
{"curie": "MONDO:0005028", "names": ["Adenocarcinoma", "adenocarcinoma esophagus", "Esophagus Adenocarcinoma", "esophagus adenocarcinoma", "adenocarcinoma oesophagus", "Esophageal Adenocarcinoma", "adenocarcinoma esophageal", "Esophageal adenocarcinoma", "esophageal adenocarcinoma", "adenocarcinoma - esophagus", "Adenocarcinoma - esophagus", "oesophageal adenocarcinoma", "Oesophageal adenocarcinoma", "Adenocarcinoma of esophagus", "adenocarcinoma of esophagus", "Adenocarcinoma of Esophagus", "ADENOCARCINOMA OF ESOPHAGUS", "Adenocarcinoma Of Esophagus", "Adenocarcinoma of oesophagus", "Esophageal adenocarcinoma NOS", "Oesophageal adenocarcinoma NOS", "Oesophageal Adenocarcinoma NOS", "adenocarcinoma of the esophagus", "Adenocarcinoma of the Esophagus", "cancer esophagus adenocarcinoma", "Adenocarcinoma of the esophagus", "esophagus cancer, adenocarcinoma", "esophageal cancer, adenocarcinoma", "Adenocarcinoma of esophagus (disorder)", "adenocarcinoma of esophagus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophageal adenocarcinoma", "shortest_name_length": 14}
{"curie": "UMLS:C2981398", "names": ["Stage IIA Colorectal Cancer", "Stage IIA Colorectal Cancer AJCC v7", "Stage IIA Colorectal (Colon or Rectal) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Colorectal Cancer AJCC v7", "shortest_name_length": 27}
{"curie": "MONDO:0018342", "names": ["JBTS with JATD", "Joubert syndrome with JATD", "Joubert syndrome with Jeune asphyxiating thoracic dystrophy", "Joubert syndrome with JATD (Jeune asphyxiating thoracic dystrophy)", "Joubert syndrome with Jeune asphyxiating thoracic dystrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome with Jeune asphyxiating thoracic dystrophy", "shortest_name_length": 14}
{"curie": "UMLS:C2217677", "names": ["thyroid cancer stage II", "Thyroid cancer stage II", "malignant tumor of thyroid stage II", "malignant neoplasm of thyroid stage II", "malignant neoplasm of thyroid stage II (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid cancer stage II", "shortest_name_length": 23}
{"curie": "MONDO:0006918", "names": ["Choroiditis", "posterior uveitis", "Posterior uveitis", "Uveitis, Posterior", "Uveitis, posterior", "uveitis, posterior", "chorioretinal region inflammation", "inflammation of chorioretinal region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "posterior uveitis", "shortest_name_length": 11}
{"curie": "MONDO:0010316", "names": ["FGS3", "FG SYNDROME 3", "FG syndrome 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FG syndrome 3", "shortest_name_length": 4}
{"curie": "MONDO:0015315", "names": ["neonatal brainstem dysfunction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal brainstem dysfunction", "shortest_name_length": 30}
{"curie": "UMLS:C0002883", "names": ["Anemia, Hemolytic, Idiopathic Acquired"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anemia, Hemolytic, Idiopathic Acquired", "shortest_name_length": 38}
{"curie": "MONDO:0014241", "names": ["ALL3", "ALL 3", "ALL, Susceptibility, 3", "susceptibility to acute lymphoblastic leukemia 3", "PAX5 precursor B-cell acute lymphoblastic leukemia", "Acute Lymphoblastic Leukemia Susceptibility - PAX5", "Acute Lymphoblastic Leukemia, Susceptibility to, 3", "leukemia, acute lymphoblastic, susceptibility to, 3", "LEUKEMIA, ACUTE LYMPHOBLASTIC, SUSCEPTIBILITY TO, 3", "leukemia, acute lymphoblastic, susceptibility to, type 3", "precursor B-cell acute lymphoblastic leukemia caused by mutation in PAX5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukemia, acute lymphoblastic, susceptibility to, 3", "shortest_name_length": 4}
{"curie": "MONDO:0033637", "names": ["MC4DN7", "mitochondrial complex 4 deficiency, nuclear type 7", "MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 7", "mitochondrial complex IV deficiency, nuclear type 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 4 deficiency, nuclear type 7", "shortest_name_length": 6}
{"curie": "UMLS:C4528549", "names": ["Breast Cancer by AJCC v8 Anatomic Stage", "Breast Carcinoma by AJCC v8 Anatomic Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Cancer by AJCC v8 Anatomic Stage", "shortest_name_length": 39}
{"curie": "UMLS:C4727827", "names": ["Refractory Soft Tissue Sarcoma, Excluding Rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Soft Tissue Sarcoma, Excluding Rhabdomyosarcoma", "shortest_name_length": 58}
{"curie": "MONDO:0002256", "names": ["cervix disease", "Cervix Disease", "Disorder cervix", "cervix disorder", "Cervix Diseases", "Cervix disorder", "CERVIX DISORDER", "DISORDER CERVIX", "Disease, Cervix", "CERVIX DISORDERS", "cervical disease", "Diseases, Cervix", "cervix disorders", "Cervix Disorders", "Disease of cervix", "Cervical Disorder", "cervical disorder", "cervical diseases", "disorder of cervix", "cervical disorders", "Disorder of cervix", "Cervical disease nos", "Cervical disorder NOS", "uterine cervix disease", "Disease of cervix, NOS", "Uterine disorder cervix", "UTERINE DISORDER CERVIX", "DISORDER UTERINE CERVIX", "Disorder of cervix, NOS", "Disorder uterine cervix", "Uterine Cervix Disorders", "Uterine Cervical Disease", "Cervical Disease, Uterine", "Disease, Uterine Cervical", "Uterine Cervical Diseases", "disease of uterine cervix", "Disorder of uterine cervix", "disorder of uterine cervix", "Cervical Diseases, Uterine", "Diseases, Uterine Cervical", "disease (or disorder); cervix", "Uterine cervical disorder NOS", "CERVIX UTERINE DISORDER (NOS)", "disorder of cervix (diagnosis)", "Disease of uterine cervix, NOS", "Disorder of uterine cervix, NOS", "Cervicitis/other cervical disease", "uterine cervix disease or disorder", "Disorder of uterine cervix (disorder)", "Disease or syndrome of uterine cervix", "disease or disorder of uterine cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervix disorder", "shortest_name_length": 14}
{"curie": "UMLS:C2825560", "names": ["S-Beta Thalassemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "S-Beta Thalassemia", "shortest_name_length": 18}
{"curie": "MONDO:0019350", "names": ["Anemia spherocytic", "ANEMIA SPHEROCYTIC", "Spherocytic anemia", "spherocytic anemia", "Minkowski-Chauffard", "Anaemia spherocytic", "anemia; spherocytic", "Spherocytic anaemia", "ANAEMIA SPHEROCYTIC", "spherocytic; anemia", "familial spherocytosis", "Familial spherocytosis", "SPHEROCYTOSIS HEREDITARY", "hereditary spherocytosis", "HEREDITARY SPHEROCYTOSIS", "Hereditary spherocytosis", "Hereditary Spherocytosis", "CONGENITAL SPHEROCYTOSIS", "congenital spherocytosis", "Congenital spherocytosis", "Hereditary Spherocytoses", "spherocytosis hereditary", "SPHEROCYTOSIS, HEREDITARY", "Spherocytoses, Hereditary", "Spherocytosis, Hereditary", "Minkowski-Chauffard disease", "Familial acholuric jaundice", "Minkowski-Chauffard syndrome", "spherocytic hemolytic anemia", "Minkowsky-Chauffard syndrome", "Minkowski Chauffard syndrome", "MINKOWSKI-CHAUFFARD SYNDROME", "Hereditary spherocytosis, NOS", "Acholuric (familial) jaundice", "HS - Hereditary spherocytosis", "hereditary hemolytic spherocytosis", "Hereditary spherocytosis (disorder)", "hereditary spherocytosis (diagnosis)", "Congenital spherocytic hemolytic anemia", "congenital spherocytic hemolytic anemia", "ANEMIA, HEMOLYTIC, HEREDITARY SPHEROCYTIC", "Congenital spherocytic haemolytic anaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spherocytosis", "shortest_name_length": 18}
{"curie": "UMLS:C4054588", "names": ["Lymphocytic Neurohypophysitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphocytic Neurohypophysitis", "shortest_name_length": 29}
{"curie": "UMLS:C0338478", "names": ["Idiopathic Myoclonic Epilepsy", "Idiopathic myoclonic epilepsy", "Cryptogenic Myoclonic Epilepsy", "Myoclonic Epilepsy, Idiopathic", "Cryptogenic myoclonic epilepsy", "Epilepsy, Idiopathic Myoclonic", "Myoclonic Epilepsy, Cryptogenic", "Idiopathic Myoclonic Epilepsies", "Epilepsy, Cryptogenic Myoclonic", "Cryptogenic Myoclonic Epilepsies", "Myoclonic Epilepsies, Idiopathic", "Epilepsies, Idiopathic Myoclonic", "Epilepsies, Cryptogenic Myoclonic", "Myoclonic Epilepsies, Cryptogenic", "Idiopathic myoclonic epilepsy (disorder)", "Cryptogenic myoclonic epilepsy (disorder)", "Idiopathic myoclonic epilepsy (diagnosis)", "epilepsy generalized cryptogenic myoclonic", "Cryptogenic myoclonic epilepsy (diagnosis)", "epilepsy generalized cryptogenic idiopathic myoclonic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Idiopathic Myoclonic Epilepsy", "shortest_name_length": 29}
{"curie": "MONDO:0000833", "names": ["bone remodeling disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bone remodeling disease", "shortest_name_length": 23}
{"curie": "MONDO:0005891", "names": ["Ostertagiases", "ostertagiasis", "Ostertagiasis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ostertagiasis", "shortest_name_length": 13}
{"curie": "MONDO:0018230", "names": ["skeletal dysplasia", "primary osteodysplasia", "primary bone dysplasia", "primary skeletal dysplasia", "Mendelian skeletal dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skeletal dysplasia", "shortest_name_length": 18}
{"curie": "UMLS:C1332937", "names": ["Childhood M6 Leukemia", "Pediatric M6 Leukemia", "Acute Erythroid Leukemia", "childhood acute M6 leukemia", "pediatric acute M6 leukemia", "M6 leukemia, childhood acute", "pediatric acute erythroleukemia", "acute erythroleukemia, childhood", "erythroleukemia, childhood acute", "leukemia, pediatric acute erythro-", "Childhood Acute Erythroid Leukemia", "M6 pediatric acute erythroleukemia", "M6 childhood acute erythroleukemia", "leukemia, childhood acute erythro-", "Pediatric Acute Erythroid Leukemia", "childhood acute erythroleukemia (M6)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Acute Erythroid Leukemia", "shortest_name_length": 21}
{"curie": "UMLS:C0152889", "names": ["adrenal tuberculosis", "Adrenal gland tuberculosis", "Adrenal Gland Tuberculosis", "tuberculosis of adrenal gland", "Tuberculosis of adrenal glands", "adrenal; tuberculous (etiology)", "tuberculosis; adrenal (etiology)", "adrenal; tuberculous (manifestation)", "tuberculosis; adrenal (manifestation)", "tuberculosis of adrenal gland (diagnosis)", "Tuberculosis of adrenal glands (disorder)", "Tuberculosis of adrenal glands, unspecified", "Tuberculosis of adrenal glands, unspecified examination"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tuberculosis of adrenal glands", "shortest_name_length": 20}
{"curie": "MONDO:0001482", "names": ["testicular leukemia", "Testicular Leukemia", "testicular leukemia (diagnosis)", "leukemia lymphocytic acute (all) in relapse testicular leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular leukemia", "shortest_name_length": 19}
{"curie": "UMLS:C1511304", "names": ["Breast Carcinoma with Osteoclastic Giant Cells", "Breast Carcinoma with Osteoclast-Like Stromal Giant Cells"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Carcinoma with Osteoclast-Like Stromal Giant Cells", "shortest_name_length": 46}
{"curie": "MONDO:0017767", "names": ["ARF", "Rheumatic fever", "RHEUMATIC FEVER", "rheumatic fever", "Rheumatic Fever", "Fever, Rheumatic", "Acute rheumatism", "Rheumatic Fevers", "acute rheumatism", "rheumatism acute", "Rheumatic Arthritis", "Rheumatic fever, NOS", "Arthritis, Rheumatic", "Rheumatic Arthritides", "RhF - Rheumatic fever", "Acute Rheumatic Fever", "ACUTE RHEUMATIC FEVER", "RHF - rheumatic fever", "acute rheumatic fever", "RHEUMATIC FEVER ACUTE", "Acute rheumatic fever", "Rheumatic fever, acute", "Acute rheumatic attack", "Fever, Acute Rheumatic", "RHEUMATIC FEVER, ACUTE", "Acute Rheumatic Fevers", "Active rheumatic fever", "Rheumatic Fever, Acute", "Fevers, Acute Rheumatic", "Inflammatory Rheumatism", "Rheumatic fever, active", "inflammatory rheumatism", "Inflammatory rheumatism", "Rheumatism, Inflammatory", "Inflammatory Rheumatisms", "polyarthritis rheumatica", "RHEUMATISM, INFLAMMATORY", "Polyarthritis Rheumatica", "Rheumatic arthritis acute", "Acute Rheumatic Arthritis", "Acute rheumatic arthritis", "RHEUMATIC ARTHRITIS ACUTE", "Polyarthritis Rheumaticas", "Acute Articular Rheumatism", "Rheumatic Arthritis, Acute", "Acute articular rheumatism", "Arthritis, Acute Rheumatic", "Rheumatic fever (disorder)", "ARF - Acute rheumatic fever", "rheumatic fever (diagnosis)", "Rheumatism, Acute Articular", "Acute Rheumatic Arthritides", "ARF - acute rheumatic fever", "Acute Articular Rheumatisms", "Arthritis, Rheumatic, Acute", "Articular Rheumatism, Acute", "Rheumatism, Articular, Acute", "extracardiac rheumatic fever", "Acute rheumatic fever (I00-I02)", "Acute rheumatic fever (disorder)", "acute rheumatic fever (diagnosis)", "Rheumatic fever without heart involvement", "rheumatic fever without heart involvement", "acute rheumatic fever with acute arthritis", "Acute rheumatic fever with acute arthritis", "Acute arthritis due to acute rheumatic fever", "Rheumatic fever without heart involvement (disorder)", "Rheumatic fever without mention of heart involvement", "Acute rheumatic fever with acute arthritis (disorder)", "rheumatic fever without heart involvement (diagnosis)", "acute rheumatic fever with acute arthritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rheumatic fever", "shortest_name_length": 3}
{"curie": "UMLS:C1336400", "names": ["Nasopharyngeal Keratinizing Squamous Cell Carcinoma Stage IVC", "Stage IVC Nasopharyngeal Keratinizing Squamous Cell Carcinoma", "Stage IVC Nasopharyngeal Throat Keratinizing Squamous Cell Cancer", "Stage IVC Nasopharyngeal Keratinizing Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Nasopharyngeal Keratinizing Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 61}
{"curie": "UMLS:C0585274", "names": ["Periodic syndrome", "periodic syndrome", "periodic syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "periodic syndrome", "shortest_name_length": 17}
{"curie": "MONDO:0100246", "names": ["migraine with or without aura, susceptibility", "migraine with or without aura, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "migraine with or without aura, susceptibility to", "shortest_name_length": 45}
{"curie": "MONDO:0009590", "names": ["MLDSAPB", "Saposin B deficiency", "Saposin B Deficiency", "SAPOSIN B DEFICIENCY", "saposin B deficiency", "Sphingolipid activator protein I deficiency", "Sphingolipid activator protein 1 deficiency", "SAPI - Sphingolipid activator protein I deficiency", "metachromatic leukodystrophy due to sap-B deficiency", "Sphingolipid activator protein 1 deficiency (disorder)", "metachromatic leukodystrophy due to saposin b deficiency", "METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY", "metachromatic leukodystrophy due to saposin B deficiency", "Metachromatic Leukodystrophy due to Saposin B Deficiency", "Metachromatic Leukodystrophy due to Cerebroside Sulfatase Activator Deficiency", "metachromatic leukodystrophy due to cerebroside sulfatase activator deficiency", "METACHROMATIC LEUKODYSTROPHY DUE TO CEREBROSIDE SULFATASE ACTIVATOR DEFICIENCY", "Metachromatic leucodystrophy due to deficiency of cerebroside sulfatase activator", "Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator", "Metachromatic leucodystrophy due to deficiency of cerebroside sulphatase activator", "Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metachromatic leukodystrophy due to saposin B deficiency", "shortest_name_length": 7}
{"curie": "MONDO:0007916", "names": ["Waldmann disease", "Waldmann's disease", "lymphangiectasia, intestinal", "Intestinal lymphatic obstruction", "familial Waldmann's disease (type)", "primary intestinal lymphangiectasia", "Primary intestinal lymphangiectasia", "primary intestinal lymphangiectasis", "Primary intestinal lymphangiectasis", "Primary lymphangiectasis of intestine", "Primary lymphangiectasis of intestine (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary intestinal lymphangiectasia", "shortest_name_length": 16}
{"curie": "UMLS:C0406782", "names": ["Transient neonatal pustulosis", "Transient neonatal pustular melanosis", "Transient Neonatal Pustular Melanosis", "Transient neonatal pustulosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transient neonatal pustulosis", "shortest_name_length": 29}
{"curie": "MONDO:0031219", "names": ["BTPS1", "CMMRDS", "BTP1 syndrome", "MMR deficiency", "Turcot syndrome", "CMMR-D syndrome", "childhood cancer syndrome", "mismatch repair cancer syndrome", "brain tumor-polyposis syndrome 1", "constitutional mismatch repair deficiency syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mismatch repair cancer syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0271678", "names": ["Diabetic mononeuropathy", "Diabetic Mononeuropathy", "Mononeuropathy, Diabetic", "Diabetic Mononeuropathies", "Mononeuropathies, Diabetic", "Diabetic Mononeuropathy Simplex", "Diabetic mononeuropathy simplex", "Mononeuropathy Simplex, Diabetic", "Simplex, Diabetic Mononeuropathy", "Diabetic Mononeuropathy Simplices", "Simplices, Diabetic Mononeuropathy", "Mononeuropathy Simplices, Diabetic", "Mononeuropathy due to diabetes mellitus", "Diabetic mononeuropathy simplex (diagnosis)", "Mononeuropathy simplex with diabetes mellitus", "Mononeuropathy simplex due to diabetes mellitus", "diabetes mellitus diabetic mononeuropathy simplex", "Mononeuropathy due to diabetes mellitus (disorder)", "Mononeuropathy simplex due to diabetes mellitus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diabetic Mononeuropathy", "shortest_name_length": 23}
{"curie": "UMLS:C0558400", "names": ["Cerebral trauma", "cerebral trauma", "Cerebral trauma (disorder)", "cerebral trauma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebral trauma", "shortest_name_length": 15}
{"curie": "UMLS:C0521172", "names": ["Eschar", "eschar", "eschars", "eschars were seen", "eschars (physical finding)", "Eschar (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eschar", "shortest_name_length": 6}
{"curie": "UMLS:C3272778", "names": ["Appendix Kaposi Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Appendix Kaposi Sarcoma", "shortest_name_length": 23}
{"curie": "MONDO:0019324", "names": ["PF", "Cazenave", "pemphigus foliaceus", "Pemphigus Foliaceus", "Pemphigus foliaceus", "Pemphigus, foliaceus", "pemphigus foliaceous", "Foliaceus, Pemphigus", "Pemphigus foliaceous", "pemphigus; foliaceous", "foliaceous; pemphigus", "PF - Pemphigus foliaceous", "Pemphigus foliaceus (disorder)", "pemphigus foliaceus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pemphigus foliaceus", "shortest_name_length": 2}
{"curie": "UMLS:C1512858", "names": ["Intermediate Grade B-Cell Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intermediate Grade B-Cell Non-Hodgkin's Lymphoma", "shortest_name_length": 48}
{"curie": "MONDO:0010203", "names": ["Wolff Zimmermann syndrome", "Wolff-Zimmermann syndrome", "Mental retardation Wolff type", "Wolff type Mental retardation", "WOLFF mental retardation syndrome", "Wolff mental retardation syndrome", "WOLFF MENTAL RETARDATION SYNDROME", "Intellectual disability Wolff type", "Intellectual disability, Wolff type", "intellectual disability, Wolff type", "intellectual disabilities Wolff type", "WOLFF intellectual disability syndrome", "Intellectual disability Wolff type (disorder)", "Intellectual disability Wolff type (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, Wolff type", "shortest_name_length": 25}
{"curie": "UMLS:C0852932", "names": ["Arthropod sting"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arthropod sting", "shortest_name_length": 15}
{"curie": "MONDO:0012786", "names": ["CJMG", "CTRCT47", "cataract 47", "CATARACT 47", "CJMG, FORMERLY", "CATARACT, JUVENILE, WITH MICROCORNEA", "cataract, juvenile, with microcornea", "cataract 47, juvenile, with microcornea", "Cataract, Juvenile, With Microcornea And Glucosuria", "cataract, juvenile, with microcornea and glucosuria", "Juvenile cataract-microcornea-renal glucosuria syndrome", "juvenile cataract-microcornea-renal glucosuria syndrome", "Juvenile cataract-microcornea-renal glycosuria syndrome", "Juvenile cataract, microcornea, renal glucosuria syndrome", "cataract, juvenile, with microcornea and glucosuria, formerly", "CATARACT, JUVENILE, WITH MICROCORNEA AND GLUCOSURIA, FORMERLY", "Juvenile cataract, microcornea, renal glucosuria syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile cataract-microcornea-renal glucosuria syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0012853", "names": ["FPS", "GCMS", "GCM syndrome", "Petty syndrome", "FONTAINE PROGEROID SYNDROME", "Fontaine progeroid syndrome", "Progeroid syndrome Petty type", "Gorlin Chaudhry Moss syndrome", "Gorlin-Chaudhry-Moss syndrome", "progeroid syndrome Petty type", "GORLIN-CHAUDHRY-MOSS SYNDROME", "progeroid syndrome, Petty type", "Progeroid syndrome, Petty type", "Petty-Laxova-Wiedemann syndrome", "Petty Laxova Wiedemann syndrome", "Gorlin-Chaudhry-Moss syndrome (disorder)", "progeroid syndrome congenital Petty type", "[OBSOLETE] Gorlin Chaudhry Moss syndrome", "Progeroid syndrome Petty type (disorder)", "progeroid syndrome, congenital, Petty type", "PROGEROID SYNDROME, CONGENITAL, PETTY TYPE", "Progeroid Syndrome, Congenital, Petty Type", "craniofacial dysostosis-genital, dental, cardiac anomalies syndrome", "Craniofacial dysostosis-genital, dental, cardiac anomalies syndrome", "craniofacial dysostosis, hypertrichosis, hypoplasia of labia majora", "Cranofacial dysostosis-hypertrichosis-hypoplasia of labia majora syndrome", "cranofacial dysostosis-hypertrichosis-hypoplasia of labia majora syndrome", "dental and eye anomalies, patent ductus arteriosus, and normal intelligence", "Dental and eye anomalies-patent ductus arteriosus-normal intelligence syndrome", "dental and eye anomalies-patent ductus arteriosus-normal intelligence syndrome", "craniofacial dysostosis, patent ductus arteriosus, hypertrichosis, hypoplasia of labia majora, dental and eye anomalies", "Craniofacial dysostosis, patent ductus arteriosus, hypertrichosis, hypoplasia of labia majora, dental and eye anomalies", "CRANIOFACIAL DYSOSTOSIS, HYPERTRICHOSIS, HYPOPLASIA OF LABIA MAJORA, DENTAL AND EYE ANOMALIES, PATENT DUCTUS ARTERIOSUS, AND NORMAL INTELLIGENCE", "craniofacial dysostosis, hypertrichosis, Hypoplasia of labia majora, dental and eye anomalies, patent ductus arteriosus, and normal intelligence"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fontaine progeroid syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C4525661", "names": ["Stage I Ileal Neuroendocrine Tumor", "Stage I Ileal Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Ileal Neuroendocrine Tumor AJCC v8", "shortest_name_length": 34}
{"curie": "MONDO:0015468", "names": ["craniosynostosis-cataract syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniosynostosis-cataract syndrome", "shortest_name_length": 34}
{"curie": "UMLS:C0346396", "names": ["Retinoma", "Retinocytoma", "Retinoma (disorder)", "Retinocytoma (disorder)", "Retinocytoma (diagnosis)", "eye neoplasm benign retinocytoma", "Adenoma of retinal pigment epithelium", "Retinocytoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retinoma", "shortest_name_length": 8}
{"curie": "UMLS:C1511268", "names": ["Borderline Ovarian Serous Papillary Cystic Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Ovarian Serous Papillary Cystic Tumor", "shortest_name_length": 48}
{"curie": "UMLS:C0919661", "names": ["Alternation", "alternation", "Heart alternation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Heart alternation", "shortest_name_length": 11}
{"curie": "UMLS:C1704219", "names": ["DGCT", "Dentinoma", "Dentinoameloblastoma", "Deninogenic ghost cell tumor", "Odontogenic Ghost Cell Tumor", "Odontogenic ghost cell tumor", "Dentinogenic Ghost Cell Tumor", "Odontogenic ghost cell tumour", "Dentinogenic ghost cell tumor", "Deninogenic ghost cell tumour", "Dentinogenic ghost cell tumour", "Odontogenic ghost cell neoplasm", "Dentinogenic ghost cell neoplasm", "Calcifying Ghost Cell Odontogenic Tumor", "Odontogenic ghost cell neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dentinogenic Ghost Cell Tumor", "shortest_name_length": 4}
{"curie": "MONDO:0015462", "names": ["Sharma-Kapoor-Ramji syndrome", "Sharma Kapoor Ramji syndrome", "thin ribs-tubular bones-dysmorphism syndrome", "Thin ribs-tubular bones-dysmorphism syndrome", "Thin ribs, tubular bones, dysmorphism syndrome", "Thin ribs, tubular bones, dysmorphism syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thin ribs-tubular bones-dysmorphism syndrome", "shortest_name_length": 28}
{"curie": "EFO:0009460", "names": ["ACPA-negative rheumatoid arthritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ACPA-negative rheumatoid arthritis", "shortest_name_length": 34}
{"curie": "MONDO:0100326", "names": ["Glanzmann thrombasthenia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Glanzmann thrombasthenia", "shortest_name_length": 24}
{"curie": "MONDO:0009022", "names": ["ACC", "Callosal agenesis", "Absent corpus callosum", "Corpus Callosum Absence", "corpus callosum; absent", "agenesis corpus callosum", "absence; corpus callosum", "Corpus Callosum Agenesis", "CORPUS CALLOSUM AGENESIS", "agenesis callosum corpus", "Corpus callosum agenesis", "corpus callosum agenesis", "Corpus Callosum Absences", "Corpus Callosum Ageneses", "Agenesis corpus callosum", "corpus callosum; agenesis", "Agenesis, Corpus Callosum", "CORPUS CALLOSUM, AGENESIS", "agenesis; corpus callosum", "Ageneses, Corpus Callosum", "Corpus Callosum Dysgenesis", "Corpus Callosum Dysgeneses", "Absence of corpus callosum", "Absence of Corpus Callosum", "Corpus Callosum Hypogeneses", "Dysgeneses, Corpus Callosum", "Agenesis of corpus callosum", "Dysgenesis, Corpus Callosum", "Corpus Callosum Hypogenesis", "agenesis of corpus callosum", "Agenesis of Corpus Callosum", "Corpus Callosum, Agenesis Of", "Corpus callosum, agenesis of", "Hypogeneses, Corpus Callosum", "CORPUS CALLOSUM, AGENESIS OF", "corpus callosum, agenesis of", "Hypogenesis, Corpus Callosum", "Absence of the corpus callosum", "Hypogenesis of corpus callosum", "agenesis of the corpus callosum", "Agenesis of the corpus callosum", "ACC - Agenesis of corpus callosum", "isolated corpus callosum agenesis", "Dysplastic or absent corpus callosum", "Congenital absence of corpus callosum", "Agenesis of corpus callosum (disorder)", "agenesis of corpus callosum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corpus callosum, agenesis of", "shortest_name_length": 3}
{"curie": "UMLS:C0015799", "names": ["feminization", "FEMINIZATION", "feminisation", "Feminization", "Feminisation", "Feminizations", "Feminized male", "Feminised male", "Feminization, NOS", "Male Feminization", "Feminization in Boys", "Feminization (finding)", "Feminized male (finding)", "Abnormal development of female secondary sexual characteristics", "Abnormal development of female secondary sexual characteristics (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Feminization", "shortest_name_length": 12}
{"curie": "MONDO:0011193", "names": ["COD3", "CORD14", "Cone Dystrophy 3", "CONE DYSTROPHY 3", "GUCA1A, TYR99CYS", "cone dystrophy 3", "cone dystrophy-3", "cone dystrophy type 3", "Cone-Rod Dystrophy 14", "cone-rod dystrophy 14", "CONE-ROD DYSTROPHY 14", "GUCA1A cone dystrophy", "retinal cone dystrophy", "Retinal Cone Dystrophy", "RETINAL CONE DYSTROPHY", "CONE DYSTROPHY 3 (disorder)", "cone dystrophy caused by mutation in GUCA1A", "CONE DYSTROPHY 3, TYR99CYS (allelic variant)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cone dystrophy 3", "shortest_name_length": 4}
{"curie": "UMLS:C1394254", "names": ["Cryptitis", "cryptitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cryptitis", "shortest_name_length": 9}
{"curie": "UMLS:C3897513", "names": ["Stage IVB Rectal Cancer", "Stage IVB Rectal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Rectal Cancer AJCC v7", "shortest_name_length": 23}
{"curie": "MONDO:0021206", "names": ["chronic nonsuppurative otitis media", "chronic non-suppurative otitis media", "Chronic non-suppurative otitis media", "non-suppurative otitis media, chronic", "otitis; media, nonsuppurative, chronic", "otitis; media, chronic, nonsuppurative", "Chronic nonsuppurative otitis media NOS", "Chronic non-suppurative otitis media (disorder)", "chronic nonsuppurative otitis media (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic non-suppurative otitis media", "shortest_name_length": 35}
{"curie": "MONDO:0010156", "names": ["SPG20", "Troyer syndrome", "TROYER SYNDROME", "Troyer syndrome (TS)", "spastic paraplegia 20", "Cross-McKusick syndrome", "spastic paraplegia type 20", "Troyer syndrome (disorder)", "Troyer syndrome (diagnosis)", "hereditary spastic paraplegia 20", "spastic paraplegia 20 (Troyer syndrome)", "autosomal recessive spastic paraplegia 20", "Spastic paraplegia 20, autosomal recessive", "SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE", "spastic paraplegia 20, autosomal recessive", "Spastic paraplegia with distal muscle wasting", "Autosomal recessive spastic paraplegia type 20", "autosomal recessive spastic paraplegia type 20", "autosomal recessive spastic paraplegia Troyer type", "Spastic paraplegia, autosomal recessive, Troyer type", "spastic paraplegia, autosomal recessive, Troyer type", "SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE", "childhood-onset spastic paraparesis with distal muscle wasting", "Spastic Paraparesis, Childhood-Onset, With Distal Muscle Wasting", "spastic paraparesis, childhood-onset, with distal muscle wasting", "SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING", "Spastic paraparesis, childhood onset, with distal muscle wasting", "Childhood-onset spastic paraparesis-distal muscle wasting syndrome", "childhood-onset spastic paraparesis-distal muscle wasting syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Troyer syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C1278821", "names": ["Peripheral nerve infection", "Infectious peripheral neuropathy", "Peripheral Nervous System Infectious Disorder", "Infectious disease with peripheral neuropathy", "Infectious disorder of the peripheral nervous system", "Infectious disorder of the peripheral nervous system (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peripheral Nervous System Infectious Disorder", "shortest_name_length": 26}
{"curie": "MONDO:0018942", "names": ["MMF", "Macrophagic myofasciitis", "macrophagic myofasciitis", "MMF - Macrophagic myofasciitis", "Macrophagic myofasciitis, childhood", "Macrophagic myofasciitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macrophagic myofasciitis", "shortest_name_length": 3}
{"curie": "UMLS:C5391440", "names": ["PICS", "postintensive care syndrome", "Post intensive care syndrome", "Post-Intensive Care Syndrome", "post-intensive care syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postintensive care syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C1302798", "names": ["Grade 2 Squamous Intraepithelial Lesion", "Grade II Squamous Intraepithelial Lesion", "Grade 2 Squamous Intraepithelial Neoplasia", "Squamous intraepithelial neoplasia grade 2", "Grade II Squamous Intraepithelial Neoplasia", "Squamous intraepithelial neoplasia, grade II", "Squamous intraepithelial neoplasia grade 2 (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Squamous intraepithelial neoplasia grade 2", "shortest_name_length": 39}
{"curie": "UMLS:C0521579", "names": ["Congenital squint", "Congenital strabismus", "Strabismus congenital", "STRABISMUS CONGENITAL", "Congenital strabismus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital strabismus", "shortest_name_length": 17}
{"curie": "UMLS:C4726556", "names": ["Myeloid Neoplasms with Germline Predisposition Associated with Telomerase Biology Disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myeloid Neoplasms with Germline Predisposition Associated with Telomerase Biology Disorders", "shortest_name_length": 91}
{"curie": "MONDO:0019034", "names": ["accessory pancreas", "Accessory pancreas", "accessory; pancreas", "pancreas; accessory", "Pancreas accessorium", "pancreas accessorium", "Supernumerary pancreas", "Accessory pancreas (disorder)", "accessory pancreas (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "accessory pancreas", "shortest_name_length": 18}
{"curie": "UMLS:C4725048", "names": ["Recurrent Soft Tissue Sarcoma, Excluding Rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Soft Tissue Sarcoma, Excluding Rhabdomyosarcoma", "shortest_name_length": 57}
{"curie": "MONDO:0011219", "names": ["ECTD8", "ectodermal dysplasia 8", "Fried tooth and nail syndrome", "Fried's tooth and nail syndrome", "Fried's tooth and nail syndrome (disorder)", "ECTODERMAL DYSPLASIA 8, HAIR/TOOTH/NAIL TYPE", "ectodermal dysplasia 8, hair/tooth/nail type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fried's tooth and nail syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0022765", "names": ["chronic demyelinizing neuropathy with IgM monoclonal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic demyelinizing neuropathy with IgM monoclonal", "shortest_name_length": 52}
{"curie": "MONDO:0014814", "names": ["FASPS3", "advanced sleep phase syndrome 3", "PER3 advanced sleep phase syndrome", "advanced sleep phase syndrome type 3", "familial advanced sleep phase syndrome 3", "advanced sleep phase syndrome, familial, 3", "ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 3", "advanced sleep phase syndrome, familial, type 3", "advanced sleep phase syndrome caused by mutation in PER3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "advanced sleep phase syndrome 3", "shortest_name_length": 6}
{"curie": "UMLS:C0520757", "names": ["Delayed Return of Consciousness", "Delayed Recovery from Anesthesia", "Delayed recovery from anesthetic", "Delayed recovery from anesthesia", "Delayed recovery from anaesthesia", "Delayed recovery from anaesthetic", "Delayed Emergence from Anesthesia", "Delayed Awakening from Anesthesia", "Post-Anesthesia Delayed Awakening", "Post-Procedural Delayed Awakening", "Drowsiness prolonged postoperative", "Post-Anesthesia Residual Paralysis", "Delayed Awakening, Post Procedural", "Delayed Awakening, Post-Procedural", "Delayed Regaining of Consciousness", "Post-Anesthesia Residual Paralyses", "Post-Anesthesia Delayed Awakenings", "Delayed Awakening, Post-Anesthesia", "Awakening, Post-Anesthesia Delayed", "Post-Procedural Delayed Awakenings", "Delayed Awakening, Post Anesthesia", "Residual Paralyses, Post-Anesthesia", "Delayed Awakenings, Post-Anesthesia", "Paralysis, Post-Anesthesia Residual", "Awakenings, Post-Anesthesia Delayed", "Delayed Awakenings, Post-Procedural", "Residual Paralysis, Post-Anesthesia", "Residual Paralysis, Post Anesthesia", "Paralyses, Post-Anesthesia Residual"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Delayed Emergence from Anesthesia", "shortest_name_length": 31}
{"curie": "MONDO:0009222", "names": ["GWC", "GOLLOP-WOLFGANG COMPLEX", "Gollop Wolfgang complex", "Gollop-Wolfgang complex", "Femur bifid with monodactylous ectrodactyly", "femur bifid with monodactylous ectrodactyly", "Bifid femur with monodactylous ectrodactyly", "bifid femur-monodactylous ectrodactyly syndrome", "Bifid femur-monodactylous ectrodactyly syndrome", "FEMUR, UNILATERAL BIFID, WITH MONODACTYLOUS ECTRODACTYLY", "Femur, Unilateral Bifid, With Monodactylous Ectrodactyly", "femur, unilateral bifid, with monodactylous ectrodactyly", "Bifid femur co-occurrent with monodactylous ectrodactyly", "Bifid femur co-occurrent with monodactylous ectrodactyly (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gollop-Wolfgang complex", "shortest_name_length": 3}
{"curie": "UMLS:C4727687", "names": ["Advanced Laryngeal Squamous Cell Carcinoma", "Advanced Laryngeal Throat Squamous Cell Cancer", "Advanced Squamous Cell Carcinoma of the Larynx"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Laryngeal Squamous Cell Carcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0008170", "names": ["ca ovarian", "Ovarian Ca", "ovarian ca", "ovary cancer", "cancer ovary", "Ovary Cancer", "Cancer, Ovary", "Ovary Cancers", "cancer ovarian", "OVARIAN CANCER", "cancer ovaries", "ovary neoplasm", "Ovarian Cancer", "Cancers, Ovary", "ovarian cancer", "Ovarian cancer", "cancer of ovary", "carcinoma ovary", "ovary carcinoma", "Ovarian Cancers", "Cancer of Ovary", "cancers ovarian", "ovarian cancers", "Cancer, Ovarian", "Ovaries--Cancer", "Cancer of ovary", "Cancers, Ovarian", "ovarian neoplasm", "ovarian carcinoma", "carcinoma ovarian", "Ovarian Neoplasms", "carcinoma ovaries", "tumor of the ovary", "ovarian carcinomas", "Ovarian cancer NOS", "tumor of the Ovary", "carcinoma of ovary", "Ovarian cancer, NOS", "cancer of the ovary", "Cancer of the Ovary", "CA - Cancer of ovary", "primary ovarian cancer", "Ovarian malignant tumor", "Malignant Ovarian Tumor", "malignant ovaries tumor", "ovarian cancer, somatic", "malignant Ovarian tumor", "malignant ovarian tumor", "ovarian malignant tumor", "malignant tumor of ovary", "Malignant tumor of ovary", "malignant ovary neoplasm", "Malignant Tumor of Ovary", "ovarian epithelial cancer", "Ovarian epithelial cancer", "malignant tumour of ovary", "Malignant tumour of ovary", "Epithelial ovarian cancer", "epithelial ovarian cancer", "ovarian cancer epithelial", "cancer epithelial ovarian", "Epithelial cancer of ovary", "Malignant Ovarian Neoplasm", "ovarian cancer (diagnosis)", "ovarian cancer, epithelial", "malignant ovarian neoplasm", "OVARIAN CANCER, EPITHELIAL", "Malignant neoplasm of ovary", "malignant neoplasm of ovary", "Malignant Neoplasm of Ovary", "malignant tumor of the ovary", "Malignant Tumor of the Ovary", "Ovarian epithelial cancer NOS", "Malignant Neoplasm of the Ovary", "malignant neoplasm of the ovary", "Ovarian malignant epithelial tumor", "Malignant epithelial tumor of ovary", "Malignant tumor of ovary (disorder)", "malignant neoplasm of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian cancer", "shortest_name_length": 10}
{"curie": "MONDO:0010044", "names": ["SPG15", "KJELLIN SYNDROME", "Kjellin syndrome", "spastic paraplegia 15", "hereditary spastic paraplegia 15", "hereditary spastic paraplegia type 15", "Hereditary spastic paraparesis type 15", "hereditary spastic paraparesis type 15", "autosomal recessive spastic paraplegia 15", "spastic paraplegia 15, autosomal recessive", "SPASTIC PARAPLEGIA 15, AUTOSOMAL RECESSIVE", "Spastic paraplegia 15, autosomal recessive", "spastic paraplegia and retinal Degeneration", "SPASTIC PARAPLEGIA AND RETINAL DEGENERATION", "Spastic paraplegia and retinal degeneration", "spastic paraplegia and retinal degeneration", "autosomal recessive spastic paraplegia type 15", "Autosomal recessive spastic paraplegia type 15", "Spastic paraplegia-retinal degeneration syndrome", "spastic paraplegia-retinal degeneration syndrome", "Spastic paraplegia, retinal degeneration syndrome", "ZFYVE26 autosomal recessive complex spastic paraplegia", "recessive spastic paraplegia with retinal degeneration", "Recessive spastic paraplegia with retinal degeneration", "familial spastic paraplegia autosomal recessive type 15", "Autosomal recessive spastic paraplegia type 15 (disorder)", "Autosomal recessive spastic paraplegia type 15 (diagnosis)", "autosomal recessive complex spastic paraplegia caused by mutation in ZFYVE26"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 15", "shortest_name_length": 5}
{"curie": "MONDO:0024305", "names": ["hyperprolactinemia", "hyperprolactinaemia", "Chiari-Frommel syndrome", "acquired hyperprolactinemia", "pregnancy-related A-G syndrome", "Pregnancy-related A-G syndrome", "acquired hyperprolactinemia (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired hyperprolactinemia", "shortest_name_length": 18}
{"curie": "MONDO:0009417", "names": ["Lubinsky syndrome", "HYPOGONADISM-CATARACT SYNDROME", "hypogonadism cataract syndrome", "hypogonadism-cataract syndrome", "Hypogonadism-Cataract Syndrome", "CATARACTS AND TESTICULAR FAILURE", "cataracts and testicular failure", "Cataracts and testicular failure", "Cataract and testicular failure syndrome", "Hypergonadotropic hypogonadism-cataract syndrome", "hypergonadotropic hypogonadism-cataract syndrome", "Hypergonadotropic hypogonadism with cataract syndrome", "Hypergonadotropic hypogonadism with cataract syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypergonadotropic hypogonadism-cataract syndrome", "shortest_name_length": 17}
{"curie": "UMLS:C0418178", "names": ["Radiation Overexposure", "overexposure radiation", "Overexposure to radiation", "Overexposure to radiation (event)", "overexposure to radiation (non-specific)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radiation Overexposure", "shortest_name_length": 22}
{"curie": "MONDO:0012506", "names": ["ARVD11", "ARVC11", "arrhythmogenic right ventricular dysplasia 11", "arrhythmogenic right ventricular cardiomyopathy 11", "ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 11", "arrhythmogenic right ventricular dysplasia type 11", "Arrhythmogenic Right Ventricular Cardiomyopathy 11", "familial arrhythmogenic right ventricular dysplasia 11", "arrhythmogenic right ventricular dysplasia, familial, 11", "Arrhythmogenic Right Ventricular Dysplasia, Familial, 11", "ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11", "arrhythmogenic right ventricular dysplasia, familial, type 11", "DSC2 familial isolated arrhythmogenic right ventricular dysplasia", "familial isolated arrhythmogenic right ventricular dysplasia caused by mutation in DSC2", "arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and woolly hair", "arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair", "arrhythmogenic right ventricular dysplasia, familial, 11, and mild palmoplantar keratoderma with or without woolly hair", "ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11, AND MILD PALMOPLANTAR KERATODERMA WITH OR WITHOUT WOOLLY HAIR"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arrhythmogenic right ventricular dysplasia 11", "shortest_name_length": 6}
{"curie": "MONDO:0005056", "names": ["keratinizing epidermoid carcinoma", "Keratinizing epidermoid carcinoma", "Keratinising epidermoid carcinoma", "Epidermoid carcinoma, keratinizing", "Epidermoid carcinoma, keratinising", "Keratinising squamous cell carcinoma", "Keratinizing squamous cell carcinoma", "keratinizing squamous cell carcinoma", "Keratinizing Squamous Cell Carcinoma", "squamous cell carcinoma, keratinizing", "Squamous cell carcinoma, keratinising", "Squamous cell carcinoma, keratinizing", "Epidermoid carcinoma, keratinizing type", "Squamous cell carcinoma, keratinizing NOS", "Squamous cell carcinoma, keratinizing type", "Squamous cell carcinoma, keratinizing, NOS", "Squamous cell carcinoma, keratinizing type NOS", "Squamous cell carcinoma, keratinising type NOS", "keratinizing squamous cell carcinoma (diagnosis)", "Squamous cell carcinoma, large cell, keratinizing", "[M]Squamous cell carcinoma, keratinising type NOS", "[M]Squamous cell carcinoma, keratinizing type NOS", "Squamous cell carcinoma, large cell, keratinising", "Keratinizing squamous cell carcinoma - large cell", "Keratinising squamous cell carcinoma - large cell", "Squamous cell carcinoma, large cell, keratinizing type", "squamous cell carcinoma, keratinizing (morphologic abnormality)", "Squamous cell carcinoma, keratinizing (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratinizing squamous cell carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0044992", "names": ["Oral mucosal disorder", "mouth mucosa disorder", "Disease of oral mucosa", "disease of mouth mucosa", "disorder of mouth mucosa", "oral mucous membrane disease", "Disorder of oral mucous membrane", "disorder of oral mucous membrane", "mouth mucosa disease or disorder", "disease or disorder of mouth mucosa", "Disorder of oral mucous membrane (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mouth mucosa disorder", "shortest_name_length": 21}
{"curie": "UMLS:C1403404", "names": ["Non-Burkitt's Lymphoma", "lymphoma; non-Burkitt's"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Burkitt's Lymphoma", "shortest_name_length": 22}
{"curie": "MONDO:0007986", "names": ["MTD", "Metatropic dwarf", "Dwarf, metatropic", "Metatrophic dwarf", "METATROPIC DWARFISM", "metatropic dwarfism", "Metatropic dwarfism", "METATROPIC DYSPLASIA", "Metatropic Dysplasia", "metatropic; dwarfism", "metatropic dysplasia", "dysplasia metatropic", "dwarfism; metatropic", "Metatropic dysplasia", "Metatrophic dysplasia", "metatrophic dysplasia", "Metatropic dysplasia group", "Metatropic dwarfism syndrome", "Metatrophic dwarfism syndrome", "Metatropic dysplasia (disorder)", "Metatropic dysplasia, nonlethal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metatropic dysplasia", "shortest_name_length": 3}
{"curie": "MONDO:0020469", "names": ["48,XYYY", "48,XYYY syndrome", "48,XYYY syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "48,XYYY syndrome", "shortest_name_length": 7}
{"curie": "MONDO:0100099", "names": ["R-CPD", "retrograde cricopharyngeus dysfunction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retrograde cricopharyngeus dysfunction", "shortest_name_length": 5}
{"curie": "UMLS:C0280148", "names": ["Stage II Diffuse Mixed Cell Lymphoma", "stage II adult diffuse mixed cell lymphoma", "Adult Diffuse Mixed Cell Lymphoma Stage II", "Stage II Adult Diffuse Mixed Cell Lymphoma", "adult diffuse mixed cell lymphoma, stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Adult Diffuse Mixed Cell Lymphoma", "shortest_name_length": 36}
{"curie": "MONDO:0010165", "names": ["Ulna hypoplasia with mental retardation", "ulna hypoplasia with mental retardation", "ulnar hypoplasia with mental retardation", "Ulnar Hypoplasia with Mental Retardation", "ULNAR HYPOPLASIA WITH MENTAL RETARDATION", "ulna hypoplasia with intellectual disability", "ulnar hypoplasia with intellectual disability", "ulna hypoplasia-intellectual disability syndrome", "bilateral ulnar hypoplasia and mental retardation", "Bilateral ulnar hypoplasia and mental retardation", "bilateral ulnar hypoplasia and intellectual disability", "mesomelia of the upper limbs, absent nails, clubfeet, and mental retardation", "Mesomelia of the upper limbs, absent nails, clubfeet, and mental retardation", "mesomelia of the upper limbs, absent nails, clubfeet, and intellectual disability", "mesomelia of the upper limbs, anonychia congenita, clubfeet, and mental retardation", "MESOMELIA OF THE UPPER LIMBS, ANONYCHIA CONGENITA, CLUBFEET, AND MENTAL RETARDATION", "mesomelia of the upper limbs, anonychia congenita, clubfeet, and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ulna hypoplasia-intellectual disability syndrome", "shortest_name_length": 39}
{"curie": "MONDO:0020081", "names": ["macrophage or histiocytic tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macrophage or histiocytic tumor", "shortest_name_length": 31}
{"curie": "MONDO:0006323", "names": ["non-seminomatous lesion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-seminomatous lesion", "shortest_name_length": 23}
{"curie": "UMLS:C4520763", "names": ["Stage III Sinonasal Squamous Cell Carcinoma AJCC v6 and v7", "Stage III Nasal Cavity and Paranasal Sinus Squamous Cell Cancer", "Stage III Nasal Cavity and Paranasal Sinus Squamous Cell Carcinoma", "Stage III Nasal Cavity and Paranasal Sinus Squamous Cell Carcinoma AJCC v7", "Stage III Nasal Cavity and Paranasal Sinus Squamous Cell Carcinoma AJCC v6", "Stage III Nasal Cavity and Paranasal Sinus Squamous Cell Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Sinonasal Squamous Cell Carcinoma AJCC v6 and v7", "shortest_name_length": 58}
{"curie": "MONDO:0032651", "names": ["FINCA", "FINCA syndrome", "FIBROSIS, NEURODEGENERATION, AND CEREBRAL ANGIOMATOSIS", "fibrosis, neurodegeneration, and cerebral angiomatosis", "Fibrosis-neurodegeneration-cerebral angiomatosis syndrome", "Interstitial lung fibrosis-neurodegeneration-cerebral angiomatosis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibrosis, neurodegeneration, and cerebral angiomatosis", "shortest_name_length": 5}
{"curie": "MONDO:0017310", "names": ["Marfan and Marfan-related disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Marfan and Marfan-related disorder", "shortest_name_length": 34}
{"curie": "MONDO:0003788", "names": ["childhood embryonal testis carcinoma", "Childhood Embryonal Carcinoma of Testis", "Pediatric Embryonal Carcinoma of Testis", "pediatric embryonal carcinoma of testis", "childhood embryonal carcinoma of testis", "pediatric testicular Embryonal carcinoma", "pediatric testicular embryonal carcinoma", "Pediatric Testicular Embryonal Carcinoma", "Childhood Testicular Embryonal Carcinoma", "childhood testicular embryonal carcinoma", "testicular embryonal carcinoma of childhood", "Childhood Embryonal Carcinoma of the Testis", "pediatric embryonal carcinoma of the testis", "childhood embryonal carcinoma of the testis", "Pediatric Embryonal Carcinoma of the Testis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood embryonal testis carcinoma", "shortest_name_length": 36}
{"curie": "UMLS:C4683409", "names": ["Thyroid Gland Follicular Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Follicular Carcinoma by AJCC v7 Stage", "shortest_name_length": 51}
{"curie": "MONDO:0012275", "names": ["FVS", "Fetal valproic syndrome", "FETAL VALPROATE SYNDROME", "Fetal valproate syndrome", "fetal valproate syndrome", "Fetal Valproate Syndrome", "Valproic acid embryopathy", "valproic acid embryopathy", "Foetal valproate syndrome", "foetal valproate syndrome", "FOETAL VALPROATE SYNDROME", "Epival, Fetal Effects From", "Dalpro, Fetal Effects From", "Fetal valproic acid syndrome", "fetal valproic acid syndrome", "foetal valproic acid syndrome", "fetal valproate syndrome (FVS)", "Fetal valproate spectrum disorder", "Valproic acid antenatal infection", "Foetal valproate spectrum disorder", "Fetal valproate syndrome (disorder)", "susceptibility to valproate embryopathy", "Congenital malformation due to valproate", "VALPROATE EMBRYOPATHY, SUSCEPTIBILITY TO", "valproate embryopathy, susceptibility to", "VALPROATE EMBRYOPATHY, SUSCEPTIBILITY TO (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fetal valproate syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0006935", "names": ["Subpulmonary stenosis", "Subvalvar pulmonic stenosis", "Obstructive Subaortic Conus", "Subaortic Conus, Obstructive", "Conus, Obstructive Subaortic", "Subvalvar pulmonary stenosis", "Subvalvular pulmonic stenosis", "subvalvular pulmonic stenosis", "Infundibular pulmonic stenosis", "Subvalvular Pulmonary Stenosis", "Pulmonary Subvalvular Stenoses", "pulmonary subvalvular stenosis", "Subvalvular Pulmonary Stenoses", "Pulmonary Subvalvular Stenosis", "infundibular pulmonic stenosis", "Subvalvular pulmonary stenosis", "Stenoses, Pulmonary Subvalvular", "Pulmonary Infundibular Stenoses", "Infundibular pulmonary stenosis", "Subvalvular Stenoses, Pulmonary", "Pulmonary Stenoses, Subvalvular", "Stenosis, Pulmonary Subvalvular", "Subvalvular Stenosis, Pulmonary", "Pulmonary Infundibular Stenosis", "pulmonary infundibular stenosis", "Pulmonary Stenosis, Subvalvular", "Stenosis, Subvalvular Pulmonary", "Stenoses, Subvalvular Pulmonary", "Pulmonary infundibular stenosis", "congenital infundibular stenosis", "Stenosis, Pulmonary Infundibular", "Infundibular Stenosis, Pulmonary", "Stenoses, Pulmonary Infundibular", "Congenital Infundibular Stenosis", "Congenital infundibular stenosis", "Infundibular Stenoses, Pulmonary", "stenosis; pulmonary, infundibular", "Infundibular pulmonic stenosis, congenital", "infundibular pulmonic stenosis, congenital", "Congenital infundibular pulmonary stenosis", "Stenosis of infundibulum of right ventricle", "Stenosis of infundibulum of right ventricle (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary subvalvular stenosis", "shortest_name_length": 21}
{"curie": "MONDO:0001788", "names": ["Nutmeg liver", "liver nutmeg", "nutmeg liver", "congestive; liver", "liver; congestive", "liver; sclerosis, cardiac", "sclerosis; liver, cardiac", "chronic passive hepatic congestion", "chronic passive congestion of liver", "Chronic passive congestion of liver", "Chronic Passive Congestion of Liver", "Chronic passive congestion of liver (disorder)", "chronic passive hepatic congestion (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nutmeg liver", "shortest_name_length": 12}
{"curie": "MONDO:0004264", "names": ["gonococcal endometritis", "Gonococcal endometritis", "Endometritis gonococcal", "Uterus - acute gonorrhea", "Uterus - acute gonorrhoea", "uterus - acute gonorrhoea", "acute gonorrhea of uterus", "Acute gonorrhea of uterus", "endometritis gonococcal acute", "Acute gonococcal endometritis", "acute gonococcal endometritis", "gonococcal endometritis (acute)", "Gonococcal endometritis (acute)", "Gonococcal endometritis (disorder)", "gonococcal endometritis (diagnosis)", "Acute gonococcal endometritis (disorder)", "Acute gonococcal endometritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute gonococcal endometritis", "shortest_name_length": 23}
{"curie": "UMLS:C0936247", "names": ["Brain Embolism and Thrombosis", "Embolism and Thrombosis, Brain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brain Embolism and Thrombosis", "shortest_name_length": 29}
{"curie": "UMLS:C5420041", "names": ["Sinonasal Seromucinous Hamartoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Seromucinous Hamartoma", "shortest_name_length": 32}
{"curie": "UMLS:C0242217", "names": ["Calcium Pyrophosphate Dihydrate Deposition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Calcium Pyrophosphate Dihydrate Deposition", "shortest_name_length": 42}
{"curie": "UMLS:C1336450", "names": ["Stage I Bladder Urothelial Cancer", "Stage I Bladder Urothelial Carcinoma", "Bladder transitional cell carcinoma stage I", "Stage I Bladder Urothelial Carcinoma AJCC v7", "Stage I Bladder Urothelial Carcinoma AJCC v6", "Stage I Transitional Cell Carcinoma of Bladder", "Stage I Transitional Cell Carcinoma of the Bladder", "Stage I Bladder Urothelial Carcinoma AJCC v6 and v7", "Stage I Urinary Bladder Transitional Cell Carcinoma", "Stage I Transitional Cell Carcinoma of Urinary Bladder", "Stage I Transitional Cell Carcinoma of the Urinary Bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder transitional cell carcinoma stage I", "shortest_name_length": 33}
{"curie": "MONDO:0005967", "names": ["Spleen tuberculosis", "Splenic Tuberculosis", "Splenic Tuberculoses", "splenic tuberculosis", "Tuberculosis, Splenic", "Tuberculoses, Splenic", "Tuberculosis of spleen", "tuberculosis of spleen", "Tuberculosis of spleen (disorder)", "tuberculosis of spleen (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "splenic tuberculosis", "shortest_name_length": 19}
{"curie": "MONDO:0001645", "names": ["Crescentic glomerulonephritis", "crescentic glomerulonephritis", "Crescentic Glomerulonephritis", "Glomerulonephritis, crescentic", "Glomerulonephritis, extracapillary", "GLOMERULONEPHRITIS, EXTRACAPILLARY", "CGN - Crescentic glomerulonephritis", "crescentic glomerulonephritis (disease)", "Idiopathic crescentic glomerulonephritis", "Crescentic glomerulonephritis (disorder)", "Idiopathic Crescentic Glomerulonephritis", "Proliferative crescentic glomerulonephritis", "Idiopathic crescentic glomerulonephritis, NOS", "Glomerulonephritis, proliferative, with crescents", "Idiopathic crescentic glomerulonephritis (diagnosis)", "proliferative glomerulonephritis acute idiopathic crescentic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "crescentic glomerulonephritis", "shortest_name_length": 29}
{"curie": "UMLS:C0860055", "names": ["Blennorrhagic Arthritis", "Blennorrhagic arthritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Blennorrhagic arthritis", "shortest_name_length": 23}
{"curie": "MONDO:0007349", "names": ["Fcas", "CAPS1", "FCAS1", "cold hypersensitivity", "cold urticaria, familial", "familial cold inflammatory syndrome 1", "CRYOPYRIN-ASSOCIATED PERIODIC SYNDROME 1", "Cryopyrin-associated periodic syndrome 1", "familial cold autoinflammatory syndrome 1", "FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 1", "Familial Cold Autoinflammatory Syndrome 1", "NLRP3 familial cold autoinflammatory syndrome", "familial cold autoinflammatory syndrome type 1", "cold-induced autoinflammatory syndrome, familial", "familial cold autoinflammatory syndrome caused by mutation in NLRP3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial cold autoinflammatory syndrome 1", "shortest_name_length": 4}
{"curie": "MONDO:0022672", "names": ["autosomal dominant cataract", "cataract congenital autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant cataract", "shortest_name_length": 27}
{"curie": "UMLS:C1710416", "names": ["Thyroid Gland Paraganglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Paraganglioma", "shortest_name_length": 27}
{"curie": "MONDO:0012036", "names": ["SLEB4", "SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 4", "systemic lupus erythematosus, susceptibility to, 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "systemic lupus erythematosus, susceptibility to, 4", "shortest_name_length": 5}
{"curie": "MONDO:0020735", "names": ["Aimah", "AIMAH1", "Adrenal Cushing syndrome", "ACTH-independent Cushing syndrome", "Acth-Independent Cushing Syndrome", "CUSHING SYNDROME, ADRENAL, DUE TO AIMAH", "Cushing Syndrome, Adrenal, Due To Aimah", "Cushing syndrome, adrenal, due to AIMAH", "Corticotropin-independent Cushing syndrome", "ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA", "Acth-Independent Macronodular Adrenal Hyperplasia", "ACTH-independent macronodular adrenal hyperplasia", "ACTH-independent macronodular adrenal hyperplasia 1", "ACTH-INDEPENDENT MACRONODULAR ADRENOCORTICAL HYPERPLASIA", "ACTH-independent macronodular adrenocortical hyperplasia", "Adrenocorticotropic hormone-independent Cushing syndrome", "Acth-Independent Macronodular Adrenocortical Hyperplasia", "CORTICOTROPIN-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA", "Corticotropin-Independent Macronodular Adrenal Hyperplasia", "corticotropin-independent macronodular adrenal hyperplasia", "ACTH-independent macronodular adrenal hyperplasia, Somatic mutation", "Adrenocorticotropic Hormone-Independent Macronodular Adrenal Hyperplasia", "adrenocorticotropic hormone-independent macronodular adrenal hyperplasia", "ADRENOCORTICOTROPIC HORMONE-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ACTH-independent macronodular adrenal hyperplasia 1", "shortest_name_length": 5}
{"curie": "UMLS:C3897763", "names": ["recurrent ovarian tumors of low malignant potential", "ovarian tumors of low malignant potential, recurrent", "Recurrent Borderline Ovarian Surface Epithelial-Stromal Tumor", "recurrent borderline ovarian surface epithelial-stromal tumor", "borderline ovarian surface epithelial-stromal tumor, recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Borderline Ovarian Surface Epithelial-Stromal Tumor", "shortest_name_length": 51}
{"curie": "MONDO:0010522", "names": ["AIH3", "AIH3, FORMERLY", "AIH3 (formerly)", "X-linked enamel hypoplasia", "ENAMEL HYPOPLASIA, X-LINKED", "enamel hypoplasia, X-linked", "amelogenesis imperfecta 3 hypoplastic type", "amelogenesis imperfecta type IE X-linked 2", "amelogenesis imperfecta  type IE X-linked 2", "amelogenesis imperfecta 3, hypoplastic type", "amelogenesis imperfecta, type IE, X-linked 2", "amelogenesis imperfecta 3, hypoplastic type, formerly", "AMELOGENESIS IMPERFECTA 3, HYPOPLASTIC TYPE, FORMERLY", "amelogenesis imperfecta 3, hypoplastic type (formerly)", "X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2", "Amelogenesis imperfecta, hypoplastic-hypomaturation, X-linked 2", "AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 2", "amelogenesis imperfecta, hypoplastic/hypomaturation, X-linked 2", "X-linked amelogenesis imperfecta hypoplastic/hypomaturation type 2", "amelogenesis imperfecta, hypoplastic/hypomaturation, X-linked type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2", "shortest_name_length": 4}
{"curie": "MONDO:0014358", "names": ["XIGIS", "MRD25", "MRD25, FORMERLY", "Xia Gibbs syndrome", "XIA-GIBBS SYNDROME", "Xia-Gibbs syndrome", "Xia-Gibbs Syndrome", "autosomal dominant mental retardation 25", "mental retardation, autosomal dominant 25", "autosomal dominant intellectual disability 25", "intellectual disability, autosomal dominant 25", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 25, FORMERLY", "AHDC1-related intellectual disability-obstructive sleep apnea-mild dysmorphism syndrome", "AHDC1-related intellectual disability, obstructive sleep apnea, mild dysmorphism syndrome", "AHDC1-related intellectual disability, obstructive sleep apnoea, mild dysmorphism syndrome", "AHDC1-related intellectual disability - obstructive sleep apnea - mild dysmorphism syndrome", "AT-hook DNA binding motif containing 1-related intellectual disability, obstructive sleep apnea, mild dysmorphism syndrome", "AT-hook DNA binding motif containing 1-related intellectual disability, obstructive sleep apnoea, mild dysmorphism syndrome", "AT-hook DNA binding motif containing 1-related intellectual disability, obstructive sleep apnea, mild dysmorphism syndrome (disorder)", "AT-hook DNA binding motif containing 1-related intellectual disability, obstructive sleep apnea, mild dysmorphism syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AHDC1-related intellectual disability - obstructive sleep apnea - mild dysmorphism syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0017573", "names": ["female pseudohermaphroditism-anorectal anomalies syndrome", "46,XX disorder of sex development-anorectal anomalies syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XX disorder of sex development-anorectal anomalies syndrome", "shortest_name_length": 57}
{"curie": "MONDO:0018264", "names": ["OCA6", "Shep4", "SHEP4", "Oculocutaneous albinism type 6", "albinism oculocutaneous type 6", "oculocutaneous albinism type 6", "oculocutaneous albinism type VI", "albinism, oculocutaneous, type VI", "ALBINISM, OCULOCUTANEOUS, TYPE VI", "Oculocutaneous albinism type 6 (disorder)", "oculocutaneous albinism type 6 (diagnosis)", "Skin-Hair-Eye Pigmentation, Variation In, 4", "SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 4", "skin/hair/eye pigmentation 4, fair/dark skin", "SKIN/HAIR/EYE PIGMENTATION 4, FAIR/DARK SKIN", "Skin-Hair-Eye Pigmentation 4, Fair-Dark Skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculocutaneous albinism type 6", "shortest_name_length": 4}
{"curie": "MONDO:0016418", "names": ["MSA-c", "sporadic OPCA type 1", "MSA, cerebellar type", "multiple system atrophy, cerebellar type", "sporadic olivopontocerebellar atrophy type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple system atrophy, cerebellar type", "shortest_name_length": 5}
{"curie": "MONDO:0011430", "names": ["dusty cataract", "Dusty cataract", "pulverulent cataract", "Pulverulent cataract", "Coppock-like cataract", "Cataract, Pulverulent", "Cataracts, pulverulent", "Cataract, Coppock-Like", "Pulverulent cataract (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulverulent cataract", "shortest_name_length": 14}
{"curie": "UMLS:C2939065", "names": ["Airway edema", "Airway oedema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Airway edema", "shortest_name_length": 12}
{"curie": "UMLS:C1335017", "names": ["Non-Neoplastic Inner Ear Disease", "Non-Neoplastic Inner Ear Disorder", "Non-Neoplastic Internal Ear Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Inner Ear Disorder", "shortest_name_length": 32}
{"curie": "MONDO:0022560", "names": ["benign metastasizing leiomyoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign metastasizing leiomyoma", "shortest_name_length": 30}
{"curie": "MONDO:0015478", "names": ["paramedian facial cleft", "Tessier number 1-1 and 2-12 facial cleft"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paramedian facial cleft", "shortest_name_length": 23}
{"curie": "UMLS:C4525087", "names": ["Stage IIA Colorectal Cancer AJCC v8", "Stage IIA Colorectal Carcinoma AJCC v8", "Stage IIA Colorectal (Colon or Rectal) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Colorectal Cancer AJCC v8", "shortest_name_length": 35}
{"curie": "MONDO:0016240", "names": ["HEMIMELIA", "Hemimelia", "hemimelia", "hemimelias", "Hemimelia, NOS", "Longitudinal meromelia", "longitudinal meromelia", "Transverse deficiency of arm, elbow level"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemimelia", "shortest_name_length": 9}
{"curie": "UMLS:C1136082", "names": ["Embryo Disintegration", "Disintegration of Embryo"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Embryo Disintegration", "shortest_name_length": 21}
{"curie": "UMLS:C0855041", "names": ["Relapsed Epithelioid Sarcoma", "Epithelioid sarcoma recurrent", "Recurrent Epithelioid Sarcoma", "Epithelioid Sarcoma, Recurrent", "Relapsed Epithelioid Cell Sarcoma", "Recurrent Epithelioid Cell Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epithelioid sarcoma recurrent", "shortest_name_length": 28}
{"curie": "MONDO:0008868", "names": ["Lutz Richner Landolt syndrome", "cholestatic jaundice and renal tubular insufficiency", "Cholestatic jaundice and renal tubular insufficiency", "CHOLESTATIC JAUNDICE AND RENAL TUBULAR INSUFFICIENCY", "biliary malformation with renal tubular insufficiency", "Biliary malformation with renal tubular insufficiency", "BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY", "Biliary malformation associated with renal tubular insufficiency", "Renal tubular insufficiency, cholestatic jaundice, and multiple congenital anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "biliary malformation with renal tubular insufficiency", "shortest_name_length": 29}
{"curie": "UMLS:C5419169", "names": ["COVID-19-Associated Trigeminal Neuralgia", "SARS-CoV-2-Associated Trigeminal Neuralgia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "COVID-19-Associated Trigeminal Neuralgia", "shortest_name_length": 40}
{"curie": "MONDO:0010769", "names": ["hairy ears, Y-linked", "HAIRY EARS, Y-LINKED", "Hairy Ears, Y-Linked", "hairy ears, Y-linked, Y-linked", "HYPERTRICHOSIS PINNAE AURIS, Y-LINKED", "Hypertrichosis Pinnae Auris, Y-Linked", "hypertrichosis pinnae auris, Y-linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hairy ears, Y-linked", "shortest_name_length": 20}
{"curie": "MONDO:0007530", "names": ["electroencephalographic peculiarity: 14 and 6 per sec. positive spike phenomenon", "ELECTROENCEPHALOGRAPHIC PECULIARITY: 14 AND 6 PER SEC. POSITIVE SPIKE PHENOMENON"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "electroencephalographic peculiarity: 14 and 6 per sec. positive spike phenomenon", "shortest_name_length": 80}
{"curie": "UMLS:C4289907", "names": ["Broad Ligament Serous Cystadenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Broad Ligament Serous Cystadenoma", "shortest_name_length": 33}
{"curie": "UMLS:C4086153", "names": ["Childhood Atypical Choroid Plexus Papilloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Atypical Choroid Plexus Papilloma", "shortest_name_length": 43}
{"curie": "UMLS:C0751620", "names": ["CNS primary tumor, NOS", "Primary Central Nervous System Neoplasm", "Primary Central Nervous System Neoplasms", "Central Nervous System Neoplasms, Primary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Neoplasms, Primary", "shortest_name_length": 22}
{"curie": "UMLS:C1335570", "names": ["Pulmonary Artery Angiosarcoma", "Pulmonary Artery Hemangiosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pulmonary Artery Angiosarcoma", "shortest_name_length": 29}
{"curie": "MONDO:0010043", "names": ["SPG17", "Spg17", "dHMN5B", "disease silver", "Silver disease", "silver disease", "Silver syndrome", "SILVER SYNDROME", "spastic paraplegia 17", "Spastic paraplegia 17", "hereditary spastic paraplegia 17", "SILVER SPASTIC PARAPLEGIA SYNDROME", "Silver spastic paraplegia syndrome", "BSCL2 hereditary spastic paraplegia", "hereditary spastic paraplegia type 17", "autosomal dominant spastic paraplegia 17", "spastic paraplegia 17, autosomal dominant", "SPASTIC PARAPLEGIA 17, AUTOSOMAL DOMINANT", "distal hereditary motor neuropathy type 5B", "autosomal dominant spastic paraplegia type 17", "Autosomal dominant spastic paraplegia type 17", "Spastic paraplegia-amyotrophy of hands and feet", "spastic paraplegia-amyotrophy of hands and feet", "SPASTIC PARAPLEGIA WITH AMYOTROPHY OF HANDS AND FEET", "spastic paraplegia with amyotrophy of hands and feet", "Spastic paraplegia with amyotrophy of hands and feet", "Autosomal dominant spastic paraplegia type 17 (disorder)", "hereditary spastic paraplegia caused by mutation in BSCL2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 17", "shortest_name_length": 5}
{"curie": "UMLS:C2717905", "names": ["HAE-I", "HAE 1", "Hereditary angioedema type 1", "Hereditary Angioedema Type 1", "Deficiency of C1 Esterase Inhibitor", "C1 Esterase Inhibitor, Deficiency Of", "Hereditary Angioedema Types I and II", "Hereditary angioneurotic edema type 1", "Angioedema, Hereditary, Types I and II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hereditary Angioedema Types I and II", "shortest_name_length": 5}
{"curie": "UMLS:C3890176", "names": ["psJIA", "Psoriatic JIA", "Psoriatic Juvenile Idiopathic Arthritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Psoriatic Juvenile Idiopathic Arthritis", "shortest_name_length": 5}
{"curie": "UMLS:C4553573", "names": ["Stage III", "Stage III Renal Cell Cancer", "Stage III Renal Cell Cancer AJCC v8", "Stage III Renal Cell Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Renal Cell Cancer AJCC v8", "shortest_name_length": 9}
{"curie": "MONDO:0023066", "names": ["Wallis cremin Beighton syndrome", "enchondromatosis dwarfism deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "enchondromatosis dwarfism deafness", "shortest_name_length": 31}
{"curie": "UMLS:C2981630", "names": ["Stage IIIA Gallbladder Cancer", "Stage IIIA Gallbladder Cancer AJCC v7", "Stage IIIA Gallbladder Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Gallbladder Cancer AJCC v7", "shortest_name_length": 29}
{"curie": "MONDO:0009568", "names": ["SPG21", "MAST Syndrome", "MAST SYNDROME", "Mast syndrome", "mast syndrome", "hereditary spastic paraplegia 21", "autosomal recessive spastic paraplegia 21", "spastic paraplegia 21, autosomal recessive", "SPASTIC PARAPLEGIA 21, AUTOSOMAL RECESSIVE", "Spastic Paraplegia 21, Autosomal Recessive", "autosomal recessive spastic paraplegia type 21", "Autosomal recessive spastic paraplegia type 21", "familial spastic paraplegia autosomal recessive type 21", "Autosomal recessive spastic paraplegia type 21 (disorder)", "Autosomal recessive spastic paraplegia type 21 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mast syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C4721646", "names": ["Stage I Esophagus Adenocarcinoma", "Stage I Esophageal Adenocarcinoma", "Esophageal Adenocarcinoma, Stage I", "Oesophageal Adenocarcinoma Stage I", "Stage I Adenocarcinoma of Esophagus", "Stage I Adenocarcinoma of the Esophagus", "Stage I Esophageal Adenocarcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Esophageal Adenocarcinoma AJCC v7", "shortest_name_length": 32}
{"curie": "MONDO:0011498", "names": ["SCZD9", "schizophrenia 9", "SCHIZOPHRENIA 9", "schizophrenia type 9", "schizophrenia 9, susceptibility to", "schizophrenia 9 with or without an affective disorder", "SCHIZOPHRENIA 9 WITH OR WITHOUT AN AFFECTIVE DISORDER", "SCHIZOPHRENIA SUSCEPTIBILITY LOCUS, CHROMOSOME 1q42-RELATED", "schizophrenia susceptibility locus, chromosome 1Q42-related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schizophrenia 9", "shortest_name_length": 5}
{"curie": "UMLS:C4528653", "names": ["Esophageal Squamous Cell Carcinoma by AJCC v8 cTNM Stage", "Esophageal Squamous Cell Carcinoma by AJCC v8 Clinical Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Squamous Cell Carcinoma by AJCC v8 Clinical Stage", "shortest_name_length": 56}
{"curie": "UMLS:C2931133", "names": ["Pediatric Crohn's disease", "Crohn's disease, pediatric", "Crohn's disease in children", "Pediatric onset Crohn's disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pediatric Crohn's disease", "shortest_name_length": 25}
{"curie": "MONDO:0012403", "names": ["SLEB7", "SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 7", "systemic lupus erythematosus, susceptibility to, 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "systemic lupus erythematosus, susceptibility to, 7", "shortest_name_length": 5}
{"curie": "MONDO:0007903", "names": ["LFS", "LFL", "LFS1", "LFS3", "Sbla syndrome", "Li-Fraumeni syndrome", "Li-Fraumeni Syndrome 3", "Li-Fraumeni syndrome 3", "LI-FRAUMENI SYNDROME 1", "Li-Fraumeni Syndrome 1", "Li-Fraumeni syndrome 1", "Li-Fraumeni syndrome LFS3", "TP53 Li-Fraumeni syndrome", "Li-Fraumeni-like syndrome", "Li-Fraumeni-Like Syndrome", "LI-FRAUMENI-LIKE SYNDROME", "Li-Fraumeni syndrome LFS1", "Li-Fraumeni syndrome type 1", "Li-Fraumeni syndrome LFS1 (diagnosis)", "Li-Fraumeni syndrome LFS3 (diagnosis)", "Sarcoma family syndrome of Li and Fraumeni", "sarcoma family syndrome of 51 and Fraumeni", "Li-Fraumeni syndrome caused by mutation in TP53", "Sarcoma, Breast, Leukemia, and Adrenal Gland (SBLA) Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Li-Fraumeni syndrome 1", "shortest_name_length": 3}
{"curie": "UMLS:C4727395", "names": ["Recurrent Ovarian Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Ovarian Adenocarcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C5420280", "names": ["Neck CUP", "Neck Carcinoma of Unknown Primary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neck Carcinoma of Unknown Primary", "shortest_name_length": 8}
{"curie": "UMLS:C4289311", "names": ["FIGO Stage IVA Ovarian Cancer", "FIGO Stage IVA Ovarian Carcinoma", "stage IVA ovarian epithelial cancer", "Stage IVA Ovarian Epithelial Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Stage IVA Ovarian Cancer", "shortest_name_length": 29}
{"curie": "MONDO:0008649", "names": ["VENULAR INSUFFICIENCY, SYSTEMIC", "venular insufficiency, systemic", "Venular Insufficiency, Systemic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "venular insufficiency, systemic", "shortest_name_length": 31}
{"curie": "MONDO:0008703", "names": ["AMDG", "AMD2A", "Grebe syndrome", "Grebe dysplasia", "GREBE DYSPLASIA", "Grebe's syndrome", "hypochondrogenesis", "Hypochondrogenesis", "grebe chondrodysplasia", "Grebe chondrodysplasia", "GREBE CHONDRODYSPLASIA", "GREBE chondrodysplasia", "Type II Achondrogenesis", "type II achondrogenesis", "achondrogenesis, type II", "Achondrogenesis, Type II", "Grebe syndrome (disorder)", "Brazilian achondrogenesis", "acromesomelic dysplasia-2A", "ACHONDROGENESIS, BRAZILIAN", "Achondrogenesis, Brazilian", "acromesomelic dysplasia 2A", "achondrogenesis, Brazilian", "ACROMESOMELIC DYSPLASIA 2A", "CHONDRODYSPLASIA, GREBE TYPE", "Chondrodysplasia, Grebe type", "chondrodysplasia, Grebe type", "Langer-Saldino Achondrogenesis", "Langer-Saldino achondrogenesis", "achondrogenesis type II (formerly)", "Acromesomelic dysplasia Grebe type", "ACHONDROGENESIS, TYPE II, FORMERLY", "achondrogenesis, type II, formerly", "ACROMESOMELIC DYSPLASIA, GREBE TYPE", "Acromesomelic dysplasia, Grebe type", "acromesomelic dysplasia, Grebe type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acromesomelic dysplasia 2A", "shortest_name_length": 4}
{"curie": "UMLS:C0279957", "names": ["NHL, intermediate grade, stage I adult", "adult NHL, stage I, intermediate grade", "Stage I Intermediate Grade Adult Non-Hodgkin's Lymphoma", "non-Hodgkin's lymphoma, intermediate grade, stage I adult", "adult non-Hodgkin's lymphoma, intermediate grade, stage I", "lymphoma, intermediate grade, stage I adult non-Hodgkin's"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Intermediate Grade Adult Non-Hodgkin's Lymphoma", "shortest_name_length": 38}
{"curie": "MONDO:0023113", "names": ["familial colorectal cancer", "colorectal cancer, familial", "hereditary colorectal cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial colorectal cancer", "shortest_name_length": 26}
{"curie": "UMLS:C4528562", "names": ["Anal Fibroadenoma", "Anal Ectopic Fibroadenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anal Fibroadenoma", "shortest_name_length": 17}
{"curie": "MONDO:0005058", "names": ["leiomyosarcoma", "Leiomyosarcoma", "LEIOMYOSARCOMA", "leiomyosarcomas", "Leiomyosarcomas", "Leiomyosarcoma NOS", "Leiomyosarcoma, NOS", "LMS - Leiomyosarcoma", "leiomyosarcoma, malignant", "LEIOMYOSARCOMA, MALIGNANT", "Leiomyosarcoma (disorder)", "leiomyosarcoma (diagnosis)", "leiomyosarcoma - not uterine", "Leiomyosarcoma - not uterine", "Leiomyosarcoma (morphologic abnormality)", "leiomyosarcoma (excluding uterine leiomyosarcoma)", "Leiomyosarcoma (excluding uterine leiomyosarcoma)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leiomyosarcoma", "shortest_name_length": 14}
{"curie": "MONDO:0015246", "names": ["syndromic anorectal malformation", "syndrome associated with anorectal malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic anorectal malformation", "shortest_name_length": 32}
{"curie": "UMLS:C0701836", "names": ["Thermal burn", "thermal burn", "Thermal Burn", "Thermal burns", "thermal burns", "Thermal burn - disorder", "Thermal burn (disorder)", "thermal burns (diagnosis)", "Thermal burn (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thermal burn", "shortest_name_length": 12}
{"curie": "UMLS:C0278885", "names": ["adult low grade NHL", "adult NHL, low grade", "NHL, adult, low grade", "Low Grade Adult Non-Hodgkin's Lymphoma", "lymphoma, adult low grade non-Hodgkin's", "low grade non-Hodgkin's lymphoma, adult", "non-Hodgkin's lymphoma, adult, low grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Grade Adult Non-Hodgkin's Lymphoma", "shortest_name_length": 19}
{"curie": "MONDO:0011854", "names": ["SECRETORY DIARRHEA, MYOPATHY, AND DEAFNESS", "secretory diarrhea, myopathy, and deafness", "Secretory Diarrhea, Myopathy, and Deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secretory diarrhea, myopathy, and deafness", "shortest_name_length": 42}
{"curie": "UMLS:C4744461", "names": ["Metastatic Digestive System Neuroendocrine Carcinoma", "Metastatic Gastrointestinal System Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Digestive System Neuroendocrine Carcinoma", "shortest_name_length": 52}
{"curie": "UMLS:C0346416", "names": ["Benign paraganglioma", "Benign Paraganglioma", "PARAGANGLIOMA, BENIGN", "Paraganglioma, benign", "Benign neuroendocrine tumor", "benign neuroendocrine tumor", "Benign neuroendocrine tumour", "Benign neuroendocrine tumors", "Non-Metastatic Paraganglioma", "Paraganglioma and glomus tumor", "Benign Paraganglionic Neoplasm", "Paraganglioma and glomus tumour", "Benign Neuroendocrine Cell Tumor", "Paragangliomas and Glomus Tumors", "PARAGANGLIOMAS AND GLOMUS TUMORS", "Benign neuroendocrine tumor (disorder)", "benign neuroendocrine tumor (diagnosis)", "Paraganglioma, benign (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign neuroendocrine tumor", "shortest_name_length": 20}
{"curie": "MONDO:0014341", "names": ["CDCBM6", "CDCBM56", "complex cortical dysplasia with other brain malformations 6", "cortical dysplasia, complex, with other brain malformations 6", "CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 6", "TUBB complex cortical dysplasia with other brain malformations", "complex cortical dysplasia with other brain malformations type 6", "cortical dysplasia, Complex, with Other brain malformations type 6", "complex cortical dysplasia with other brain malformations caused by mutation in TUBB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complex cortical dysplasia with other brain malformations 6", "shortest_name_length": 6}
{"curie": "MONDO:0010471", "names": ["CDLS5", "Cornelia DE Lange syndrome 5", "Cornelia de Lange syndrome 5", "CORNELIA DE LANGE SYNDROME 5", "Cornelia De Lange syndrome type 5", "Cornelia de Lange syndrome 5, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cornelia de Lange syndrome 5", "shortest_name_length": 5}
{"curie": "UMLS:C0480664", "names": ["Assault By Sharp Object", "Assault by sharp object", "[X]Assault by sharp object"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Assault by sharp object", "shortest_name_length": 23}
{"curie": "MONDO:0044784", "names": ["myxoma", "Myxoma", "Myxoma, NOS", "MYXOMA, BENIGN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myxoma", "shortest_name_length": 6}
{"curie": "UMLS:C5446862", "names": ["Tumor Mass of the Extremity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tumor Mass of the Extremity", "shortest_name_length": 27}
{"curie": "MONDO:0005785", "names": ["Henipavirus Infection", "Henipavirus infection", "Henipavirus Infections", "Infection, Henipavirus", "henipavirus infectious disease", "Henipavirus infectious disease", "Henipavirus disease or disorder", "Infection caused by Henipavirus", "Henipavirus caused disease or disorder", "Infection caused by Henipavirus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "henipavirus infectious disease", "shortest_name_length": 21}
{"curie": "MONDO:0012239", "names": ["NEM1", "Nem1", "CAPM1", "CAP MYOPATHY 1", "Nemaline myopathy 1", "NEMALINE MYOPATHY 1", "nemaline myopathy 1", "TPM3 nemaline myopathy", "congenital myopathy 4B", "nemaline myopathy type 1", "congenital myopathy 4B, autosomal recessive", "nemaline myopathy caused by mutation in TPM3", "nemaline myopathy 1, autosomal dominant or recessive", "Nemaline myopathy caused by mutation in the tropomyosin 3 gene"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myopathy 4B, autosomal recessive", "shortest_name_length": 4}
{"curie": "UMLS:C0949103", "names": ["Catheter site pain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Catheter site pain", "shortest_name_length": 18}
{"curie": "MONDO:0019763", "names": ["LTEC3", "LTEC III", "laryngotracheoesophageal cleft type 3", "laryngo-tracheo-esophageal cleft type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laryngotracheoesophageal cleft type 3", "shortest_name_length": 5}
{"curie": "UMLS:C4745369", "names": ["Thyroid Gland Anaplastic Carcinoma, Osteoclastic Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Anaplastic Carcinoma, Osteoclastic Variant", "shortest_name_length": 56}
{"curie": "MONDO:0014851", "names": ["HCINF2", "hypercalcemia, infantile 2", "hypercalcemia, infantile, 2", "HYPERCALCEMIA, INFANTILE, 2", "Hypercalcemia, infantile, 2", "hypercalcemia, infantile, type 2", "SLC34A1 autosomal recessive infantile hypercalcemia", "autosomal recessive infantile hypercalcemia caused by mutation in SLC34A1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypercalcemia, infantile, 2", "shortest_name_length": 6}
{"curie": "MONDO:0007741", "names": ["Primary hydronephrosis", "congenital hydronephrosis", "hydronephrosis congenital", "Congenital hydronephrosis", "Congenital Hydronephrosis", "hydronephrosis; congenital", "congenital; hydronephrosis", "Congenital dilated renal pelvis", "Congenital hydronephrosis (disorder)", "congenital hydronephrosis (diagnosis)", "Congenital dilatation of the renal pelvis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital hydronephrosis", "shortest_name_length": 22}
{"curie": "UMLS:C0334295", "names": ["Adenocarcinoma in multiple adenomatous polyps", "Adenocarcinoma in Multiple Adenomatous Polyps", "[M] Adenocarcinoma in multiple adenomatous polyps", "Adenocarcinoma in situ in multiple adenomatous polyps", "Adenocarcinoma in multiple adenomatous polyps (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma in multiple adenomatous polyps", "shortest_name_length": 45}
{"curie": "MONDO:0037250", "names": ["testicular tumor, childhood", "Testicular Tumor, Childhood", "Childhood Neoplasm of Testis", "pediatric neoplasm of testis", "childhood neoplasm of testis", "Pediatric Neoplasm of Testis", "pediatric testicular neoplasm", "Childhood Testicular Neoplasm", "Pediatric Testicular Neoplasm", "childhood testicular neoplasm", "neoplasm of testis of childhood", "pediatric neoplasm of the testis", "childhood neoplasm of the testis", "Childhood Neoplasm of the Testis", "Pediatric Neoplasm of the Testis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood testicular neoplasm", "shortest_name_length": 27}
{"curie": "MONDO:0023186", "names": ["Fraser Jequier Chen syndrome", "chondrodysplasia, situs inversus totalis, cleft epiglottis and larynx, hexadactyly of hands and feet, pancreatic cystic dysplasia, renal dysplasia/abs"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fraser Jequier Chen syndrome", "shortest_name_length": 28}
{"curie": "UMLS:C4524733", "names": ["Pathologic Stage IIB Gastroesophageal Junction Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IIB Gastroesophageal Junction Adenocarcinoma AJCC v8", "shortest_name_length": 69}
{"curie": "UMLS:C1301361", "names": ["Polymorphic PTLD", "Polymorphic B-Cell Lymphoma", "Polymorphic Post-Transplant Lymphoproliferative Disorder", "Polymorphic post-transplant lymphoproliferative disorder", "Post-transplant lymphoproliferative disorder, polymorphic", "Polymorphic lymphoproliferative disorder following transplant", "Polymorphic lymphoproliferative disorder following transplant (disorder)", "Post-transplant lymphoproliferative disorder, polymorphic (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Polymorphic lymphoproliferative disorder following transplant", "shortest_name_length": 16}
{"curie": "UMLS:C3544347", "names": ["Intestinal fibrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal fibrosis", "shortest_name_length": 19}
{"curie": "MONDO:0008709", "names": ["ELEJALDE SYNDROME", "Elejalde syndrome", "acrocephalopolydactyly", "Acrocephalopolydactyly", "Acrocephalopolydactyly (disorder)", "Acrocephalopolydactylous dysplasia", "acrocephalopolydactylous dysplasia", "Acrocephalopolydactylous Dysplasia", "ACROCEPHALOPOLYDACTYLOUS DYSPLASIA", "ELEJALDE NEUROECTODERMAL MELANOLYSOSOMAL SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acrocephalopolydactyly", "shortest_name_length": 17}
{"curie": "MONDO:0030953", "names": ["SSFSC", "SSFSC2", "short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies", "short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 2", "SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 2", "shortest_name_length": 5}
{"curie": "UMLS:C0521756", "names": ["Multidirectional Nystagmus", "Multidirectional nystagmus", "nystagmus multidirectional", "Nystagmus, Multidirectional", "Multidirectional nystagmus (disorder)", "Multidirectional nystagmus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Multidirectional Nystagmus", "shortest_name_length": 26}
{"curie": "UMLS:C1096563", "names": ["Post procedural discomfort"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post procedural discomfort", "shortest_name_length": 26}
{"curie": "MONDO:0008941", "names": ["Thompson-Baraitser syndrome", "Thompson Baraitser syndrome", "hepatic fibrosis-renal cysts-intellectual disability syndrome", "cerebellar vermis aplasia with associated features suggesting SMITH-Lemli-Opitz syndrome and Meckel syndrome", "Cerebellar Vermis Aplasia with Associated Features suggesting Smith-Lemli-Opitz Syndrome and Meckel Syndrome", "CEREBELLAR VERMIS APLASIA WITH ASSOCIATED FEATURES SUGGESTING SMITH-LEMLI-OPITZ SYNDROME AND MECKEL SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatic fibrosis-renal cysts-intellectual disability syndrome", "shortest_name_length": 27}
{"curie": "MONDO:0024311", "names": ["limb bone cancer", "cancer of limb bone", "malignant limb bone neoplasm", "malignant neoplasm of limb bone", "cancer affecting bone of limb skeleton"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cancer affecting bone of limb skeleton", "shortest_name_length": 16}
{"curie": "UMLS:C0280375", "names": ["oropharynx lymphoepithelioma, stage IV", "oropharynx lymphoepithelioma, metastatic", "Stage IV Oropharyngeal Lymphoepithelioma", "oropharyngeal lymphoepithelioma, stage IV", "oropharyngeal lymphoepithelioma, metastatic", "stage IV lymphoepithelioma of the oropharynx", "lymphoepithelioma of the oropharynx, stage IV", "metastatic lymphoepithelioma of the oropharynx", "lymphoepithelioma of the oropharynx, metastatic", "Stage IV Oropharyngeal Lymphoepithelioma AJCC v7", "Stage IV Oropharyngeal Undifferentiated Carcinoma", "Stage IV Undifferentiated Oropharyngeal Throat Cancer", "Stage IV Oropharyngeal Undifferentiated Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Oropharyngeal Undifferentiated Carcinoma AJCC v7", "shortest_name_length": 38}
{"curie": "UMLS:C0742006", "names": ["Catheter infection", "CATHETER INFECTION", "infection catheter", "catheter infection", "catheters infection", "catheter infections"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Catheter infection", "shortest_name_length": 18}
{"curie": "MONDO:0000455", "names": ["Cone dystrophy", "cone dystrophy", "Cone Dystrophy", "dystrophy cone", "Dystrophy, Cone", "Cone Dystrophies", "Dystrophies, Cone", "retinal cone dystrophy", "stationary cone dystrophy", "Cone dystrophy (disorder)", "progressive cone dystrophy", "Progressive Cone Dystrophy", "Cone dystrophy (diagnosis)", "Progressive cone dystrophy", "Dystrophy, Progressive Cone", "Cone Dystrophy, Progressive", "Progressive Cone Dystrophies", "Progressive cone degeneration", "Cone Dystrophies, Progressive", "Dystrophies, Progressive Cone", "progressive cone dystrophy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cone dystrophy", "shortest_name_length": 14}
{"curie": "UMLS:C0853040", "names": ["Reaction to drug excipient", "Reaction to drug excipients"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reaction to drug excipient", "shortest_name_length": 26}
{"curie": "MONDO:0015380", "names": ["Facial dermoid cyst", "facial dermoid cyst", "Dermoid cyst of face", "dermoid cyst of face", "dermoid cyst of the face", "Dermoid cyst of the face", "Dermoid cyst of face (disorder)", "dermoid cyst of face (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "facial dermoid cyst", "shortest_name_length": 19}
{"curie": "MONDO:0033211", "names": ["diencephalic-mesencephalic junction dysplasia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diencephalic-mesencephalic junction dysplasia syndrome", "shortest_name_length": 54}
{"curie": "MONDO:0005100", "names": ["SSc", "PSS", "scleroderma", "Scleroderma", "sclerodermas", "sclerosis; system", "system; sclerosis", "Diffuse Sclerosis", "diffuse sclerosis", "SYSTEMIC SCLEROSIS", "Systemic Sclerosis", "Systemic sclerosis", "systemic sclerosis", "diffuse Scleroderma", "Sclerosis, Systemic", "systemic; sclerosis", "Diffuse Scleroderma", "sclerosis; systemic", "SCLEROSIS, SYSTEMIC", "Scleroderma syndrome", "systemic scleroderma", "Systemic Scleroderma", "Scleroderma, Diffuse", "systemic Scleroderma", "Systemic scleroderma", "Scleroderma, diffuse", "Scleroderma, systemic", "Scleroderma, Systemic", "Thibierge-Weissenbach", "SSc, diffuse sclerosis", "SSc, Diffuse Sclerosis", "Scleroderma;progressive", "progressive scleroderma", "SS - Systemic sclerosis", "progressive system sclerosis", "Progressive system sclerosis", "Systemic sclerosis (disorder)", "Progressive Systemic Sclerosis", "Progressive systemic sclerosis", "PROGRESSIVE SYSTEMIC SCLEROSIS", "Thibierge-Weissenbach syndrome", "progressive systemic sclerosis", "Systemic sclerosis, unspecified", "systemic; sclerosis, progressive", "sclerosis; systemic, progressive", "PSS (progressive systemic sclerosis)", "Scleroderma (& [systemic sclerosis])", "PSS - Progressive systemic sclerosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "systemic sclerosis", "shortest_name_length": 3}
{"curie": "OMIM:608622", "names": ["Hypertension, Diastolic, Resistance to", "HYPERTENSION, DIASTOLIC, RESISTANCE TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 38}
{"curie": "MONDO:0015484", "names": ["Coenuroses", "Coenurosis", "Cysticercosis", "Cysticercoses", "cysticercoses", "CYSTICERCOSIS", "cysticercosis", "Cysticerciasis", "Cystercercosis", "Neurocoenurosis", "Neurocoenuroses", "Larval teniasis", "Larval taeniasis", "Coenuri Infection", "neurocysticercosis", "Coenurus Infection", "Neurocysticercoses", "Coenuri Infections", "NEUROCYSTICERCOSIS", "Infection, Coenuri", "Neurocysticercosis", "Coenurus Infections", "Infection, Coenurus", "cerebral cysticercosis", "Cerebral cysticercosis", "Pork tapeworm infection", "pork tapeworm infection", "Tapeworm infection pork", "tapeworm infection: pork", "Cysticercosis (disorder)", "Larval tapeworm infection", "cysticercosis (diagnosis)", "Cysticercosis, unspecified", "Infection by tapeworm larvae", "INFECTIONS BY TAPEWORM LARVAE", "brain; cysticercosis (etiology)", "cysticercosis; brain (etiology)", "tenia solium infectious disease", "Cerebral cysticercosis (disorder)", "cerebral; cysticercosis (etiology)", "intestinal taenia solium infection", "cysticercosis; cerebral (etiology)", "Infection caused by tapeworm larvae", "cysticercosis; brain (manifestation)", "brain; cysticercosis (manifestation)", "cysticercosis; cerebral (manifestation)", "cerebral; cysticercosis (manifestation)", "Tapeworm infection intestinal taenia solum", "tapeworm infection: intestinal taenia solum", "Infection caused by tapeworm larvae (disorder)", "tapeworm infection: [intestinal taenia solium] or [pork]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cysticercosis", "shortest_name_length": 10}
{"curie": "MONDO:0016599", "names": ["autosomal dominant secondary polycythemia", "secondary polycythemia, autosomal dominant", "autosomal dominant secondary erythrocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant secondary polycythemia", "shortest_name_length": 41}
{"curie": "MONDO:0015740", "names": ["18p trisomy", "Trisomy 18p", "trisomy 18p", "18p duplication", "Duplication 18p", "trisomy type 18p", "partial trisomy 18p", "Chromosome 18, trisomy 18p", "chromosome 18p duplication", "trisomy of the short arm of chromosome 18", "Trisomy of the short arm of chromosome 18", "Duplication of the short arm of chromosome 18"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trisomy 18p", "shortest_name_length": 11}
{"curie": "MONDO:0005799", "names": ["Bunostomiases", "Bunostomiasis", "hookworm infection", "infection, hookworm", "infections, hookworm", "hookworm infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hookworm infectious disease", "shortest_name_length": 13}
{"curie": "UMLS:C1332227", "names": ["Alcohol-Related Esophageal Carcinoma", "Alcohol-Related Esophageal Squamous Cell Cancer", "Alcohol-Related Esophageal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alcohol-Related Esophageal Squamous Cell Carcinoma", "shortest_name_length": 36}
{"curie": "UMLS:C5419540", "names": ["Unresectable Distal Esophagus Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Distal Esophagus Adenocarcinoma", "shortest_name_length": 44}
{"curie": "MONDO:0011945", "names": ["Fetal Gaucher Disease", "fetal Gaucher disease", "Fetal Gaucher disease", "Gaucher disease collodion type", "Gaucher Disease, Collodion Type", "GAUCHER DISEASE, COLLODION TYPE", "Gaucher disease, collodion type", "Perinatal lethal Gaucher disease", "perinatal lethal Gaucher disease", "Gaucher disease perinatal lethal", "Gaucher disease, perinatal lethal", "Gaucher Disease, Perinatal Lethal", "GAUCHER DISEASE, PERINATAL LETHAL", "Gaucher's disease perinatal lethal", "Gaucher disease, perinatal-lethal form", "Perinatal lethal Gaucher disease (disorder)", "Gaucher disease, perinatal lethal (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gaucher disease perinatal lethal", "shortest_name_length": 21}
{"curie": "MONDO:0001819", "names": ["cranialis; polyneuritic", "CRANIAL NERVE PALSY MULTIPLE", "multiple cranial nerve palsy", "Multiple cranial nerve palsy", "Cranial nerve palsies multiple", "Multiple cranial nerve palsies", "multiple cranial nerve palsies", "disorder multiple cranial nerves", "Multiple cranial nerve palsy, NOS", "cranial nerve; disorder, multiple", "disorder of multiple cranial nerves", "Disorders of multiple cranial nerves", "Multiple cranial nerve palsy (disorder)", "multiple cranial nerve palsies (diagnosis)", "Multiple cranial nerve disease or syndrome", "Multiple Cranial Nerve Diseases and Syndromes", "disorder of multiple cranial nerves (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple cranial nerve palsy", "shortest_name_length": 23}
{"curie": "MONDO:0011553", "names": ["DFNB26", "autosomal recessive deafness 26", "deafness, autosomal recessive 26", "DEAFNESS, AUTOSOMAL RECESSIVE 26", "Deafness, Autosomal Recessive 26", "autosomal recessive nonsyndromic deafness 26", "autosomal recessive nonsyndromic hearing loss 26", "autosomal recessive nonsyndromic deafness type 26"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 26", "shortest_name_length": 6}
{"curie": "UMLS:C3897745", "names": ["Recurrent Pilomyxoid Astrocytoma", "recurrent childhood pilomyxoid astrocytoma", "Recurrent Childhood Pilomyxoid Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Pilomyxoid Astrocytoma", "shortest_name_length": 32}
{"curie": "MONDO:0013944", "names": ["APLAID", "AUTOINFLAMMATION, ANTIBODY DEFICIENCY, AND IMMUNE DYSREGULATION", "autoinflammation, antibody deficiency, and immune dysregulation syndrome", "autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation", "Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation", "AUTOINFLAMMATION, ANTIBODY DEFICIENCY, AND IMMUNE DYSREGULATION, PLCG2-ASSOCIATED", "AUTOINFLAMMATION, antibody deficiency, and immune dysregulation, PLCG2-associated", "Autoinflammation phospholipase C gamma 2 associated antibody deficiency and immune dysregulation", "APLAID - autoinflammation phospholipase C gamma 2 associated antibody deficiency and immune dysregulation", "Autoinflammation phospholipase C gamma 2 associated antibody deficiency and immune dysregulation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation", "shortest_name_length": 6}
{"curie": "UMLS:C5420252", "names": ["Refractory Ganglioneuroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Ganglioneuroblastoma", "shortest_name_length": 31}
{"curie": "MONDO:0003233", "names": ["Kinetic tremor", "TREMOR ESSENTIAL", "essential tremor", "Essential Tremor", "tremor essential", "Essential tremor", "Tremor, essential", "Essential Tremors", "Tremor, Essential", "tremor; essential", "essential; tremor", "essential tremors", "Tremors, Essential", "shaky hand syndrome", "physiological tremor", "Tremor, physiological", "essential benign tremor", "Benign essential tremor", "Benign Essential Tremor", "benign essential tremor", "essential benign tremors", "Benign Essential Tremors", "Essential Tremor, Benign", "benign essential tremors", "Tremor, Benign Essential", "PRESENILE TREMOR SYNDROME", "Tremors, Benign Essential", "Essential Tremors, Benign", "Essential tremor (disorder)", "essential hereditary tremor", "Essential tremor (diagnosis)", "tremor, hereditary essential", "Essential tremor (hereditary)", "benign essential tremor syndrome", "BENIGN ESSENTIAL TREMOR SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "essential tremor", "shortest_name_length": 14}
{"curie": "MONDO:0008744", "names": ["Frontonasal dysplasia with alar clefts", "frontonasal dysplasia with alar clefts", "FRONTONASAL DYSPLASIA WITH ALAR CLEFTS", "Coloboma of Alar-nasal cartilages with telecanthus", "coloboma of alar-nasal cartilages with telecanthus", "alar-nasal cartilages, coloboma of, with telecanthus", "ALAR-NASAL CARTILAGES, COLOBOMA OF, WITH TELECANTHUS", "Alar-Nasal Cartilages, Coloboma Of, With Telecanthus", "alar cartilages hypoplasia-coloboma-telecanthus syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alar cartilages hypoplasia-coloboma-telecanthus syndrome", "shortest_name_length": 38}
{"curie": "MONDO:0004161", "names": ["Uterine Corpus Apoplectic Leiomyoma", "uterine corpus apoplectic leiomyoma", "Uterine Corpus Hemorrhagic Cellular Leiomyoma", "uterine corpus hemorrhagic cellular leiomyoma", "uterine corpus leiomyoma with apoplectic change", "Uterine Corpus Leiomyoma with Apoplectic Change"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine corpus apoplectic leiomyoma", "shortest_name_length": 35}
{"curie": "UMLS:C0276447", "names": ["Rhinovirus", "rhinovirus", "Rhinovirus infection", "Rhinovirus Infection", "rhinovirus infection", "rhinovirus (diagnosis)", "Rhinovirus infection NOS", "Disease due to Rhinovirus", "Rhinovirus infection, NOS", "DISEASES DUE TO RHINOVIRUS", "Disease caused by Rhinovirus", "viral; infection, retrovirus", "infection; viral, retrovirus", "Disease due to Rhinovirus, NOS", "Disease caused by Rhinovirus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rhinovirus infection", "shortest_name_length": 10}
{"curie": "UMLS:C5446512", "names": ["Conjunctival Reactive Lymphoid Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conjunctival Reactive Lymphoid Hyperplasia", "shortest_name_length": 42}
{"curie": "MONDO:0016675", "names": ["DA10", "Short tendo calcaneus", "short achilles tendon", "SHORT ACHILLES TENDON", "short tendo calcaneus", "Short Achilles tendon", "short Achilles tendon", "tendo calcaneus, short", "TENDO CALCANEUS, SHORT", "Tendo Calcaneus, Short", "plantar flexion contracture", "Plantar flexion contracture", "arthrogryposis distal type 10", "Distal arthrogryposis type 10", "distal arthrogryposis type 10", "congenital plantar contractures", "CONGENITAL PLANTAR CONTRACTURES", "Arthrogryposis, Distal, Type 10", "ARTHROGRYPOSIS, DISTAL, TYPE 10", "arthrogryposis, distal, type 10", "Short Achilles tendon (disorder)", "short achilles tendon (diagnosis)", "DA10 - distal arthrogryposis type 10", "Congenital plantar flexion contracture", "Distal arthrogryposis type 10 (disorder)", "arthrogryposis distal type 10 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal arthrogryposis type 10", "shortest_name_length": 4}
{"curie": "MONDO:0019003", "names": ["MEN2", "MEA, type 2", "MEN, type 2", "MEN Type II", "MEA Type II", "PTC syndrome", "Sipple syndrome", "Sipple's syndrome", "Familial chromaffinomatosis", "Multiple Endocrine Neoplasia Type 2", "Multiple endocrine neoplasia type 2", "multiple endocrine neoplasia type 2", "Multiple endocrine neoplasia Type 2", "Multiple endocrine neoplasia, type 2", "Multiple endocrine neoplasia Type II", "type II multiple endocrine neoplasia", "multiple endocrine neoplasia, type II", "Multiple endocrine adenomatosis, type 2", "Multiple endocrine adenomatosis Type II", "Multiple endocrine neoplasia, type 2 (disorder)", "multiple endocrine neoplasia, type II (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple endocrine neoplasia type 2", "shortest_name_length": 4}
{"curie": "UMLS:C0750194", "names": ["Non-Sustained VT", "Ventricular tachycardia, unsustained", "VENTRICULAR TACHYCARDIA NON SUSTAINED", "Non-Sustained Ventricular Tachycardia", "Non-sustained ventricular tachycardia", "NON-SUSTAINED VENTRICULAR TACHYCARDIA", "Ventricular Tachycardia, Non-Sustained", "Non-Sustained Ventricular Tachycardia by EKG Finding", "Non-Sustained Ventricular Tachycardia by ECG Finding"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-sustained ventricular tachycardia", "shortest_name_length": 16}
{"curie": "MONDO:0012285", "names": ["LVNC2", "left ventricular noncompaction 2", "LEFT VENTRICULAR NONCOMPACTION 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "left ventricular noncompaction 2", "shortest_name_length": 5}
{"curie": "UMLS:C0685016", "names": ["Metastasis to trachea", "Metastases to trachea", "Metastasis to the Trachea", "Cancer metastatic to trachea", "Metastatic Tumor to the Trachea", "Metastatic Neoplasm to the Trachea", "Secondary malignant tumor of trachea", "tracheal malignant neoplasm secondary", "Secondary malignant tumour of trachea", "Secondary malignant neoplasm of trachea", "Metastatic malignant neoplasm of trachea", "Metastatic malignant neoplasm to trachea", "Secondary Malignant Tumor to the Trachea", "Secondary Malignant Neoplasm to the Trachea", "Secondary malignant neoplasm of trachea, NOS", "Metastatic Malignant Neoplasm in the Trachea", "Metastatic Malignant Neoplasm to the Trachea", "Metastatic malignant neoplasm to trachea, NOS", "Metastatic malignant neoplasm to trachea (disorder)", "Secondary malignant neoplasm of trachea (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to trachea", "shortest_name_length": 21}
{"curie": "MONDO:0032571", "names": ["SEMDK", "IMMUNOOSSEOUS DYSPLASIA, KRAKOW TYPE", "Immunoosseous Dysplasia, Krakow Type", "SPONDYLOEPIMETAPHYSEAL DYSPLASIA, KRAKOW TYPE", "spondyloepimetaphyseal dysplasia, Krakow type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepimetaphyseal dysplasia, Krakow type", "shortest_name_length": 5}
{"curie": "UMLS:C1698635", "names": ["Upper extremity dysfunction", "Upper Extremity Dysfunction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Upper extremity dysfunction", "shortest_name_length": 27}
{"curie": "MONDO:0014502", "names": ["IMD38", "immunodeficiency 38", "autosomal recessive ISG15 deficiency", "MSMD due to complete ISG15 deficiency", "ISG15 DEFICIENCY, AUTOSOMAL RECESSIVE", "ISG15 deficiency, autosomal recessive", "IMMUNODEFICIENCY 38 WITH BASAL GANGLIA CALCIFICATION", "immunodeficiency 38 with basal ganglia calcification", "IMMUNODEFICIENCY 38, MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE", "immunodeficiency 38, Mycobacteriosis, autosomal recessive", "immunodeficiency 38, mycobacteriosis, autosomal recessive", "Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency", "ISG15 autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency", "autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency caused by mutation in ISG15"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C5206806", "names": ["Advanced Myxoid Liposarcoma", "Advanced Myxoid/Round Cell Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Myxoid Liposarcoma", "shortest_name_length": 27}
{"curie": "UMLS:C1336428", "names": ["Stage IV Nodular Lymphocyte Predominant Hodgkin Lymphoma", "Stage IV Nodular Lymphocyte Predominant Hodgkin's Disease", "Stage IV Nodular Lymphocyte Predominant Hodgkin's Lymphoma", "Ann Arbor Stage IV Nodular Lymphocyte Predominant Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage IV Nodular Lymphocyte Predominant Hodgkin Lymphoma", "shortest_name_length": 56}
{"curie": "MONDO:0010761", "names": ["RPY", "retinitis pigmentosa Y-linked", "Y-linked retinitis pigmentosa", "RETINITIS PIGMENTOSA, Y-LINKED", "Retinitis Pigmentosa, Y-Linked", "retinitis pigmentosa, Y-linked", "retinitis pigmentosa, y-linked, y-linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa Y-linked", "shortest_name_length": 3}
{"curie": "UMLS:C3146258", "names": ["Stage IV Oropharyngeal Carcinoma", "Stage IV Oropharyngeal Throat Cancer", "Stage IV Oropharyngeal Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Oropharyngeal Carcinoma AJCC v7", "shortest_name_length": 32}
{"curie": "UMLS:C0157718", "names": ["eczema; ingested substance", "dermatitis due to substances taken internally", "Dermatitis due to substances taken internally", "Dermatitis caused by substance taken internally", "Dermatitis due to substances taken internally, NOS", "Dermatitis due to unspecified substance taken internally", "Dermatitis due to Unspecified Substance Taken Internally", "dermatitis due to substances taken internally (diagnosis)", "Dermatitis caused by substance taken internally (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dermatitis caused by substance taken internally", "shortest_name_length": 26}
{"curie": "UMLS:C0886483", "names": ["Malignant Ovarian Germ Cell Tumor", "malignant ovarian germ cell tumor", "childhood malignant ovarian germ cell tumor", "Childhood Malignant Ovarian Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Malignant Ovarian Germ Cell Tumor", "shortest_name_length": 33}
{"curie": "MONDO:0001377", "names": ["Vitreous syneresis", "vitreous syneresis", "Vitreal degeneration", "vitreous degeneration", "Vitreous degeneration", "Vitreous degeneration, NOS", "Vitreous syneresis (finding)", "vitreous disorders degeneration", "Vitreous degeneration (disorder)", "Vitreous degeneration (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitreous syneresis", "shortest_name_length": 18}
{"curie": "OMIM:613589", "names": ["LDLCQ6", "LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 6}
{"curie": "MONDO:0044721", "names": ["IMD52", "IMMUNODEFICIENCY 52", "immunodeficiency 52", "SCID due to LAT deficiency", "Severe combined immunodeficiency due to LAT deficiency", "severe combined immunodeficiency due to LAT deficiency", "Severe combined immunodeficiency due to linker for activation of T cells deficiency", "Severe combined immunodeficiency due to LAT (linker for activation of T cells) deficiency", "Severe combined immunodeficiency due to linker for activation of T cells deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe combined immunodeficiency due to LAT deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0007559", "names": ["Ppr", "PPR", "PPR1", "photosensitivity", "EPILEPSY, PHOTOGENIC", "epilepsy, photogenic", "PHOTOCONVULSIVE REACTION", "Photoconvulsive reaction", "PHOTOPAROXYSMAL RESPONSE 1", "photoparoxysmal response 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "photoparoxysmal response 1", "shortest_name_length": 3}
{"curie": "UMLS:C4324634", "names": ["Product use complaint"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Product use complaint", "shortest_name_length": 21}
{"curie": "UMLS:C4727367", "names": ["Recurrent Appendix Mucinous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Appendix Mucinous Adenocarcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0020478", "names": ["LHON plus disease", "Leber plus disease", "Leber plus disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leber plus disease", "shortest_name_length": 17}
{"curie": "MONDO:0005779", "names": ["HFMD", "hand mouth foot disease", "disease foot hand mouth", "mouth foot hand disease", "hand foot mouth disease", "mouth disease foot hand", "foot mouth hand disease", "foot hand mouth disease", "disease foot hands mouth", "diseases foot hand mouth", "Disease;hand foot & mouth", "Hand, Foot, Mouth Disease", "hand foot & mouth disease", "disease hand foot and mouth", "Hand Foot and Mouth Disease", "HAND-FOOT-AND-MOUTH DISEASE", "hand-foot-and-mouth disease", "Hand foot and mouth disease", "Hand-foot-and-mouth disease", "hand foot and mouth disease", "hand, foot and mouth disease", "Hand, foot and mouth disease", "Hand, Foot and Mouth Disease", "Hand, Foot, and Mouth Disease", "hand-; foot and mouth disease", "Hand, foot, and mouth disease", "foot and mouth disease; hand-", "hand, foot, and mouth disease", "disease foot mouth disorder hand", "Vesicular stomatitis and exanthem", "Vesicular stomatitis with xanthem", "vesicular stomatitis and exanthem", "Hand foot and mouth disease (disorder)", "VESICULAR STOMATITIS-EXANTHEM SYNDROME", "hand foot and mouth disease (diagnosis)", "Enteroviral vesicular stomatitis with exanthem", "exanthema; with enteroviral vesicular stomatitis", "vesicular; stomatitis, with exanthem, enteroviral", "disease (or disorder); hand-, foot and mouth disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hand, foot and mouth disease", "shortest_name_length": 4}
{"curie": "MONDO:0012793", "names": ["GOUT2", "RHUC2", "UAQTL2", "gout susceptibility 2", "GOUT SUSCEPTIBILITY 2", "HYPOURICEMIA, RENAL, 2", "Hypouricemia, Renal, 2", "hypouricemia, renal, 2", "hypouricemia, renal, type 2", "uric acid concentration, serum, QTL 2", "URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 2", "uric acid concentration, serum, quantitative trait locus 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypouricemia, renal, 2", "shortest_name_length": 5}
{"curie": "MONDO:0008778", "names": ["Bullous cutaneous amyloid", "Bullous cutaneous amyloidosis", "amyloidosis, cutaneous bullous", "Amyloidosis, Cutaneous Bullous", "AMYLOIDOSIS, CUTANEOUS BULLOUS", "Bullous cutaneous amyloidosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyloidosis, cutaneous bullous", "shortest_name_length": 25}
{"curie": "UMLS:C5446547", "names": ["Primary Ciliary Body Lymphoma", "Primary Ciliary Body Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Ciliary Body Non-Hodgkin Lymphoma", "shortest_name_length": 29}
{"curie": "MONDO:0018589", "names": ["AApoAIV amyloidosis", "renal AApoAIV amyloidosis", "apolipoprotein A-IV amyloidosis", "apolipoprotein A-IV associated amyloidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AApoAIV amyloidosis", "shortest_name_length": 19}
{"curie": "MONDO:0007608", "names": ["FIF", "DESMD", "Desmoid Tumor", "desmoid tumor", "deep fibromatosis", "Deep Fibromatosis", "desmoid fibromatosis", "Desmoid Fibromatosis", "Aggressive fibromatosis", "Aggressive Fibromatosis", "aggressive fibromatosis", "Desmoid-Type Fibromatosis", "desmoid type fibromatosis", "desmoid-type fibromatosis", "DESMOID DISEASE, HEREDITARY", "Desmoid disease, hereditary", "desmoid disease, hereditary", "desmoid disorder, hereditary", "deep fibromatosis/desmoid tumor", "Deep Fibromatosis/Desmoid Tumor", "desmoid/aggressive fibromatosis", "Familial infiltrative fibromatosis", "familial infiltrative fibromatosis", "FIBROMATOSIS, FAMILIAL INFILTRATIVE", "Fibromatosis, familial infiltrative", "fibromatosis, familial infiltrative", "Desmoid Tumor Caused By Somatic Mutation", "DESMOID TUMOR CAUSED BY SOMATIC MUTATION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "desmoid tumor", "shortest_name_length": 3}
{"curie": "UMLS:C0234302", "names": ["Anterior tongue taste disorder", "Taste disorder, anterior tongue", "Taste Disorder, Anterior Tongue", "Anterior tongue taste disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Taste Disorder, Anterior Tongue", "shortest_name_length": 30}
{"curie": "MONDO:0007523", "names": ["BJHS", "hEDS", "EDS3", "EDS 3", "EDS-HT", "HT-EDS", "EDSHMB", "EDS III", "EDS3 (formerly)", "Hypermobile EDS", "hypermobile EDS", "Hypermobile EDS (hEDS)", "BENIGN HYPERMOBILITY SYNDROME", "benign hypermobility syndrome", "Ehlers-Danlos syndrome type 3", "Benign hypermobility syndrome", "Ehlers-Danlos syndrome, type 3", "type III Ehlers-Danlos syndrome", "ehlers-danlos syndrome type iii", "Ehlers-Danlos syndrome type III", "Ehlers-Danlos syndrome, type III", "Ehlers-Danlos Syndrome, Type III", "EHLERS-DANLOS SYNDROME, TYPE III", "hypermobile Ehlers-Danlos syndrome", "Hypermobile Ehlers-Danlos syndrome", "benign joint hypermobility syndrome", "Ehlers-Danlos syndrome type 3 (formerly)", "Ehlers-Danlos syndrome, hypermobile type", "Ehlers-Danlos syndrome hypermobility type", "Ehlers-Danlos syndrome, type 3 (disorder)", "Ehlers-Danlos Syndrome, Hypermobility Type", "Ehlers-Danlos syndrome, hypermobility type", "EHLERS-DANLOS SYNDROME, HYPERMOBILITY TYPE", "Hypermobile Ehlers-Danlos syndrome (disorder)", "hypermobile Ehlers-Danlos syndrome (diagnosis)", "Ehlers-Danlos syndrome, benign hypermobile form", "Cutis hyperelastica III, benign hypermobility type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ehlers-Danlos syndrome, hypermobility type", "shortest_name_length": 4}
{"curie": "MONDO:0011094", "names": ["CMH24", "CMD1C", "CMDC1", "CMD1T", "LVNC3", "dilated cardiomyopathy 1C", "dilated cardiomyopathy 1T", "Dilated Cardiomyopathy-1C", "CARDIOMYOPATHY, DILATED, 1C", "Cardiomyopathy, Dilated, 1C", "dilated cardiomyopathy type 1C", "left ventricular noncompaction 3", "cardiomyopathy, hypertrophic, 24", "LEFT VENTRICULAR NONCOMPACTION 3", "CARDIOMYOPATHY, DILATED, 1C (disorder)", "cardiomyopathy, familial hypertrophic, 24", "CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 24", "cardiomyopathy, dilated, 1C, with or without LVNC", "dilated cardiomyopathy 1C with or without left ventricular noncompaction", "cardiomyopathy, dilated, 1C, with or without left ventricular noncompaction", "CARDIOMYOPATHY, DILATED, 1C, WITH OR WITHOUT LEFT VENTRICULAR NONCOMPACTION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1C", "shortest_name_length": 5}
{"curie": "MONDO:0000653", "names": ["integumental system cancer", "integumentary system cancer", "cancer of integumental system", "malignant integumental system neoplasm", "malignant neoplasm of integumental system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "integumentary system cancer", "shortest_name_length": 26}
{"curie": "UMLS:C1334153", "names": ["Immature Granulocytic Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immature Granulocytic Sarcoma", "shortest_name_length": 29}
{"curie": "MONDO:0016366", "names": ["maternal PKU", "maternal pku", "Maternal PKU", "PKU, Maternal", "Maternal phenylketonuria", "Maternal Phenylketonuria", "maternal phenylketonuria", "Phenylketonuria, Maternal", "phenylketonuria pregnancy", "phenylketonuria; maternal", "maternal; phenylketonuria", "PHENYLKETONURIA, MATERNAL", "Phenylketonuric embryopathy", "phenylketonuric embryopathy", "phenylketonuria in pregnancy", "Pregnancy in Phenylketonuria", "Phenylketonuria, Pregnancy in", "maternal hyperphenylalaninemia", "Maternal hyperphenylalaninemia", "Hyperphenylalaninemic embryopathy", "hyperphenylalaninemic embryopathy", "Maternal phenylketonuria (disorder)", "Maternal Phenylalanine Hydroxylase Deficiency Disease", "Phenylalanine-Hydroxylase Deficiency Disease, Maternal", "Phenylalanine Hydroxylase Deficiency Disease, Maternal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maternal phenylketonuria", "shortest_name_length": 12}
{"curie": "MONDO:0020692", "names": ["SCDO1", "vertebral anomalies", "spondylothoracic dysplasia", "spondylocostal dysostosis 1", "spondylothoracic dysostosis", "autosomal recessive spondylocostal dysostosis 1", "spondylocostal dysostosis 1, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondylocostal dysostosis 1, autosomal recessive", "shortest_name_length": 5}
{"curie": "MONDO:0020638", "names": ["SSM", "Low-CSD Melanoma", "Non- CSD Melanoma", "Pagetoid Melanoma", "pagetoid melanoma", "Low-CSD Melanoma/SSM", "melanoma superficial spreading", "Superficial Spreading Melanoma", "superficial spreading melanoma", "Superficial spreading melanoma", "SSM - Superficial spreading melanoma", "SSMM - Superficial spreading melanoma", "Superficial Spreading Melanoma of Skin", "Superficial spreading melanoma of skin", "superficial spreading melanoma of skin", "superficial spreading malignant melanoma", "Cutaneous Superficial Spreading Melanoma", "cutaneous superficial spreading melanoma", "melanoma, superficial spreading malignant", "malignant melanoma, superficial spreading", "Superficial Spreading Melanoma of the Skin", "superficial spreading melanoma of the skin", "Low Degree of Cumulative Sun Damage Melanoma", "SMM - Superficial spreading melanoma of skin", "superficial spreading malignant skin melanoma", "Superficial Spreading Malignant Skin Melanoma", "superficial spreading cutaneous (skin) melanoma", "Superficial Spreading Cutaneous (Skin) Melanoma", "Low-CSD Melanoma/Superficial Spreading Melanoma", "Superficial spreading melanoma stage unspecified", "Superficial Spreading Malignant Melanoma of Skin", "superficial spreading malignant melanoma of skin", "Superficial spreading malignant melanoma of skin", "Superficial Spreading Malignant Melanoma of the Skin", "superficial spreading malignant melanoma of the skin", "SSMM - Superficial spreading malignant melanoma of skin", "Superficial spreading melanoma (morphologic abnormality)", "Superficial spreading malignant melanoma of skin (disorder)", "superficial spreading malignant melanoma of skin (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "superficial spreading melanoma", "shortest_name_length": 3}
{"curie": "UMLS:C1519930", "names": ["Vaginal Soft Tissue Tumor", "Vaginal Soft Tissue Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Soft Tissue Neoplasm", "shortest_name_length": 25}
{"curie": "UMLS:C3272854", "names": ["Anal NET G2", "Anal Canal NET G2", "Anal Neuroendocrine Tumor G2", "Anal Canal Neuroendocrine Tumor G2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anal Canal Neuroendocrine Tumor G2", "shortest_name_length": 11}
{"curie": "MONDO:0018426", "names": ["AXIN2-related AFAP", "AXIN2-related attenuated FAP", "AXIN2-related attenuated familial polyposis coli", "AXIN2-related attenuated familial adenomatous polyposis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AXIN2-related attenuated familial adenomatous polyposis", "shortest_name_length": 18}
{"curie": "UMLS:C5205656", "names": ["Locally Advanced Leiomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Leiomyosarcoma", "shortest_name_length": 31}
{"curie": "MONDO:0019665", "names": ["Monostotic dysplasia", "Localised osteitis fibrosa", "Localized osteitis fibrosa", "Jaffe-Lichtenstein disease", "monostotic fibrous dysplasia", "Monostotic Fibrous Dysplasia", "Monostotic fibrous dysplasia", "Fibrous Dysplasia, Monostotic", "Monostotic Fibrous Dysplasias", "Dysplasia, Monostotic Fibrous", "monostotic; fibrous dysplasia", "dysplasia; fibrous, monostotic", "fibrous; dysplasia, monostotic", "Dysplasia, fibrous, monostotic", "monostotic; dysplasia, fibrous", "Fibrous dysplasia (monostotic)", "Fibrous Dysplasias, Monostotic", "Osteitis fibrosa circumscripta", "Dysplasias, Monostotic Fibrous", "osteitis; fibrosa, circumscripta", "fibrosa; osteitis, circumscripta", "monostotic fibrous dysplasia of bone", "Monostotic Fibrous Dysplasia of Bone", "monostotic fibrous dysplasia (disease)", "Monostotic fibrous dysplasia (disorder)", "monostotic fibrous dysplasia (diagnosis)", "Fibrous dysplasia (monostotic), unspecified site", "Fibrous dysplasia (monostotic), site unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "monostotic fibrous dysplasia", "shortest_name_length": 20}
{"curie": "MONDO:0008295", "names": ["PCT, Type I", "PCT, type 1", "PCT, TYPE I", "PCT, Sporadic Type", "PCT, 'SPORADIC' TYPE", "PCT, 'sporadic' type", "Acquired hepatic porphyria", "porphyria cutanea tarda type I", "Porphyria cutanea tarda type I", "porphyria cutanea tarda, type I", "PORPHYRIA CUTANEA TARDA, TYPE I", "porphyria cutanea tarda, type 1", "Porphyria Cutanea Tarda, Type I", "sporadic porphyria cutanea tarda", "Sporadic porphyria cutanea tarda", "acquired porphyria cutanea tarda", "Sporadic porphyria cutanea tarda (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sporadic porphyria cutanea tarda", "shortest_name_length": 11}
{"curie": "MONDO:0017072", "names": ["lumbosacral spina bifida cystica"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lumbosacral spina bifida cystica", "shortest_name_length": 32}
{"curie": "MONDO:0017587", "names": ["onychomatricoma", "nail matrix tumor", "tumor of nail matrix", "nail matrix neoplasm", "neoplasm of nail matrix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "onychomatricoma", "shortest_name_length": 15}
{"curie": "MONDO:0001704", "names": ["vaginal glandular tumor", "Vaginal Glandular Tumor", "Vaginal Glandular Neoplasm", "vaginal glandular neoplasm", "vagina glandular cell neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vaginal glandular neoplasm", "shortest_name_length": 23}
{"curie": "MONDO:0009106", "names": ["SCM", "SSCM", "Dimyelia", "SCM type 1", "diplomyelia", "Diastematomyelia", "diastematomyelia", "DIASTEMATOMYELIA", "Diastematomyelias", "Pseudodiplomyelia", "Split spinal cord", "Split cord malformation", "split cord malformation", "diastematomyelia (diagnosis)", "split spinal cord malformation", "Split spinal cord malformation", "split cord malformation type 1", "Split spinal cord malformation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diastematomyelia", "shortest_name_length": 3}
{"curie": "MONDO:0017106", "names": ["Retrocerebellar cyst", "retrocerebellar cyst", "Retrocerebellar arachnoid cyst", "retrocerebellar cyst (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retrocerebellar cyst", "shortest_name_length": 20}
{"curie": "MONDO:0011405", "names": ["PN", "poikiloderma with neutropenia", "Poikiloderma with Neutropenia", "POIKILODERMA WITH NEUTROPENIA", "Poikiloderma with neutropenia", "Poikiloderma with neutropenia (disorder)", "Clericuzio type poikiloderma with neutropenia", "poikiloderma with neutropenia Clericuzio type", "Poikiloderma with neutropenia Clericuzio type", "Poikiloderma with neutropenia, Clericuzio type", "poikiloderma with neutropenia, Clericuzio-type", "poikiloderma with neutropenia, Clericuzio type", "Poikiloderma with Neutropenia, Clericuzio-Type", "POIKILODERMA WITH NEUTROPENIA, CLERICUZIO-TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "poikiloderma with neutropenia", "shortest_name_length": 2}
{"curie": "MONDO:0020604", "names": ["X-linked dominant disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked dominant disease", "shortest_name_length": 25}
{"curie": "MONDO:0001975", "names": ["Orbit Cavernous Angioma", "orbit cavernous angioma", "orbit cavernous hemangioma", "Orbit Cavernous Hemangioma", "Cavernous Angioma of Orbit", "cavernous angioma of orbit", "Cavernous Angioma of orbit", "cavernous orbital hemangioma", "orbital hemangioma cavernous", "Cavernous Hemangioma of Orbit", "cavernous hemangioma of orbit", "Cavernous hemangioma of orbit", "Cavernous Angioma of the Orbit", "cavernous angioma of the orbit", "Cavernous haemangioma of orbit", "Cavernous Hemangioma of the Orbit", "cavernous hemangioma of the orbit", "cavernous orbital hemangioma (diagnosis)", "Cavernous hemangioma of orbit (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cavernous hemangioma of orbit", "shortest_name_length": 23}
{"curie": "MONDO:0011265", "names": ["HYD2", "STHAG2", "Hypodontia-Oligodontia 2", "HYPODONTIA/OLIGODONTIA 2", "hypodontia/oligodontia 2", "tooth agenesis, selective, 2", "TOOTH AGENESIS, SELECTIVE, 2", "Tooth Agenesis, Selective, 2", "TOOTH AGENESIS, SELECTIVE, 2 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tooth agenesis, selective, 2", "shortest_name_length": 4}
{"curie": "MONDO:0033482", "names": ["SCA47", "PADDAS syndrome", "spinocerebellar ataxia 47", "SPINOCEREBELLAR ATAXIA 47", "cerebellar ataxia type 47", "SCA47 - spinocerebellar ataxia type 47", "PUM1-associated developmental disability-ataxia-seizure syndrome", "PUM1-associated developmental disability, ataxia, seizure syndrome", "Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome", "Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia 47", "shortest_name_length": 5}
{"curie": "UMLS:C1706728", "names": ["Adrenal Gland Composite Pheochromocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adrenal Gland Composite Pheochromocytoma", "shortest_name_length": 40}
{"curie": "UMLS:C2981704", "names": ["Stage IIIC Eyelid Carcinoma", "Stage IIIC Eyelid Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Eyelid Carcinoma AJCC v7", "shortest_name_length": 27}
{"curie": "UMLS:C0267596", "names": ["rectal bleed", "rectorrhagia", "Rectorrhagia", "Bleeding;anal", "proctorrhagia", "Proctorrhagia", "bleeding rectum", "Rectal Bleeding", "BLEEDING RECTAL", "rectum bleeding", "rectal bleeding", "Bleeding;rectal", "Bleeding-rectal", "Bleeding rectal", "Rectal bleeding", "RECTUM BLEEDING", "RECTAL BLEEDING", "Blood per rectum", "HEMORRHAGE RECTUM", "RECTAL HEMORRHAGE", "rectum hemorrhage", "HEMORRHAGE RECTAL", "rectal blood loss", "Hemorrhage rectal", "Rectal blood loss", "Rectal Hemorrhage", "rectal hemorrhage", "Hemorrhage rectum", "Rectal hemorrhage", "Haemorrhage rectal", "Rectal haemorrhage", "HAEMORRHAGE RECTUM", "hemorrhage; rectum", "rectum; hemorrhage", "Haemorrhage rectum", "bleeding per rectum", "Bleeding per rectum", "RB - Rectal bleeding", "Hemorrhage of rectum", "Haemorrhage of rectum", "PRB - Rectal bleeding", "PR - Blood per rectum", "PR - Bleeding per rectum", "Rectal hemorrhage (disorder)", "rectal hemorrhage (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rectal hemorrhage", "shortest_name_length": 12}
{"curie": "UMLS:C1336722", "names": ["testicular teratoma with seminoma and yolk sac tumor", "testicular yolk sac tumor and teratoma with seminoma", "yolk sac tumor and teratoma with seminoma, testicular", "teratoma with seminoma and yolk sac tumor of the testis", "testis cancer, yolk sac tumor and teratoma with seminoma", "testis cancer, teratoma with seminoma and yolk sac tumor", "Mixed Yolk Sac Tumor and Teratoma with Seminoma of Testis", "testicle cancer, teratoma with seminoma and yolk sac tumor", "Testicular Mixed Yolk Sac Tumor and Teratoma with Seminoma", "testicular cancer, teratoma with seminoma and yolk sac tumor", "Mixed Yolk Sac Neoplasm and Teratoma with Seminoma of Testis", "testicular cancer, yolk sac tumor and teratoma with seminoma", "Testicular Mixed Yolk Sac Neoplasm and Teratoma with Seminoma", "Mixed Yolk Sac Tumor and Teratoma with Seminoma of the Testis", "Mixed Yolk Sac Neoplasm and Teratoma with Seminoma of the Testis", "Mixed Endodermal Sinus Tumor and Teratoma with Seminoma of Testis", "Testicular Mixed Endodermal Sinus Tumor and Teratoma with Seminoma", "Mixed Endodermal Sinus Neoplasm and Teratoma with Seminoma of Testis", "Testicular Mixed Endodermal Sinus Neoplasm and Teratoma with Seminoma", "Mixed Endodermal Sinus Tumor and Teratoma with Seminoma of the Testis", "Mixed Endodermal Sinus Neoplasm and Teratoma with Seminoma of the Testis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular Mixed Yolk Sac Tumor and Teratoma with Seminoma", "shortest_name_length": 52}
{"curie": "MONDO:0000308", "names": ["primary systemic mycosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary systemic mycosis", "shortest_name_length": 24}
{"curie": "MONDO:0005921", "names": ["malaria vivax", "vivax malaria", "Vivax malaria", "Vivax Malaria", "malaria; vivax", "Malaria, Vivax", "Malaria, vivax", "Tertian malaria", "vivax; malarial", "malaria; tertian", "tertian; malarial", "Plasmodium; vivax", "Benign tertian malaria", "malaria plasmodium vivax", "Vivax malaria (disorder)", "Plasmodium vivax malaria", "MALARIA PLASMODIUM VIVAX", "Plasmodium vivax Malaria", "malaria; Plasmodium vivax", "Malaria, Plasmodium vivax", "Malaria by Plasmodium vivax", "malaria by Plasmodium vivax", "BT - Benign tertian malaria", "Plasmodium vivax malaria NOS", "BTM - Benign tertian malaria", "Vivax malaria - benign tertian", "Vivax malaria [benign tertian]", "Vivax malaria (benign tertian)", "Plasmodium vivax malaria (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Plasmodium vivax malaria", "shortest_name_length": 13}
{"curie": "UMLS:C5418889", "names": ["Advanced Ovarian Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Ovarian Serous Adenocarcinoma", "shortest_name_length": 38}
{"curie": "UMLS:C5555622", "names": ["Ovarian Mixed Carcinoma", "Ovarian Mixed Cell Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Mixed Cell Adenocarcinoma", "shortest_name_length": 23}
{"curie": "MONDO:0004918", "names": ["Central corneal ulcer", "central corneal ulcer", "Central corneal ulcer (disorder)", "central corneal ulcer (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central corneal ulcer", "shortest_name_length": 21}
{"curie": "UMLS:C0349571", "names": ["parotid gland adenoma", "adenoma gland parotid", "Adenoma of parotid gland", "adenoma of parotid gland", "Parotid Pleomorphic Adenoma", "Pleomorphic Adenoma of Parotid", "Parotid Gland Benign Mixed Tumor", "Parotid Gland Pleomorphic Adenoma", "Pleomorphic Adenoma of the Parotid", "Benign Mixed Tumor of Parotid Gland", "Pleomorphic adenoma of parotid gland", "Pleomorphic Adenoma of Parotid Gland", "Benign Mixed Tumor of the Parotid Gland", "Pleomorphic Adenoma of the Parotid Gland", "PSA - Pleomorphic adenoma of parotid gland", "Pleomorphic adenoma of parotid gland (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pleomorphic adenoma of parotid gland", "shortest_name_length": 21}
{"curie": "UMLS:C3272726", "names": ["Circumferential Endothelial Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Circumferential Endothelial Hyperplasia", "shortest_name_length": 39}
{"curie": "UMLS:C2983706", "names": ["Colon Cancer by AJCC v6 Stage", "Colon Carcinoma by AJCC v6 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colon Cancer by AJCC v6 Stage", "shortest_name_length": 29}
{"curie": "UMLS:C2987264", "names": ["Esophageal MANEC", "Esophageal Mixed Adenoneuroendocrine Cancer", "Esophageal Mixed Adenoneuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Mixed Adenoneuroendocrine Carcinoma", "shortest_name_length": 16}
{"curie": "MONDO:0006660", "names": ["arthus reaction", "Arthus Reaction", "Arthus reaction", "Reaction, Arthus", "Arthus Phenomenon", "arthus phenomenon", "Arthus phenomenon", "ARTHUS PHENOMENON", "Phenomenon, Arthus", "arthus type urticaria", "Arthus type urticaria", "Arthus reaction, function", "arthus reaction (function)", "arthus (phenomenon or reaction)", "Arthus type urticaria (disorder)", "Arthus reaction, function (observable entity)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthus reaction", "shortest_name_length": 15}
{"curie": "UMLS:C1335305", "names": ["Pancreatic Borderline Intraductal Papillary-Mucinous Neoplasm", "pancreatic intraductal papillary mucinous neoplasm with moderate dysplasia", "intraductal papillary-mucinous neoplasm of pancreas with moderate dysplasia", "Pancreatic Intraductal Papillary-Mucinous Neoplasm with Intermediate Grade Dysplasia", "intraductal papillary-mucinous neoplasm of pancreas with moderate dysplasia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intraductal papillary-mucinous neoplasm of pancreas with moderate dysplasia", "shortest_name_length": 61}
{"curie": "MONDO:0004617", "names": ["Recurrent hypersomnia", "recurrent hypersomnia", "Recurrent Hypersomnia", "Hypersomnia, Recurrent", "Recurrent Hypersomnias", "primary recurrent hypersomnia", "Recurrent hypersomnia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "recurrent hypersomnia", "shortest_name_length": 21}
{"curie": "MONDO:0024540", "names": ["JLNS1", "Surdo-Cardiac syndrome", "Jervell and Lange-Nielsen syndrome", "Jervell And Lange-Nielsen Syndrome 1", "JERVELL AND LANGE-NIELSEN SYNDROME 1", "Jervell and Lange-Nielsen syndrome 1", "Jervell And Lange Nielsen Syndrome 1", "KCNQ1 Jervell and Lange-Nielsen syndrome", "prolonged QT interval in Ekg and sudden death", "deafness, congenital, and functional heart disease", "Cardioauditory syndrome of Jervell and Lange-Nielsen", "Jervell and Lange-Nielsen syndrome caused by mutation in KCNQ1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jervell and Lange-Nielsen syndrome 1", "shortest_name_length": 5}
{"curie": "UMLS:C0266539", "names": ["congenital cataract total", "Congenital total cataract", "Congenital cataract, total", "Total early-onset cataract", "Congenital complete cataract", "Congenital total cataract (disorder)", "Congenital total cataract (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital total cataract", "shortest_name_length": 25}
{"curie": "UMLS:C0151571", "names": ["Corneal lesion", "CORNEAL LESION", "Lesion corneal", "LESION CORNEAL", "Lesion of cornea", "Corneal lesion NOS", "Corneal lesion, NOS", "Lesion of cornea (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lesion of cornea", "shortest_name_length": 14}
{"curie": "MONDO:0001195", "names": ["fever spots", "fever spotted", "spotted fever", "Spotted Fever", "FEVER, SPOTTED", "Fever, Spotted", "spotted; fever", "spotted fevers", "fever; spotted", "fever, spotted", "Spotted fevers", "Spotted Fevers", "Fevers, Spotted", "fevers, spotted", "Spotted fever disorders", "unspecified spotted fever", "Spotted fever, unspecified", "spotted fever rickettsiosis", "Spotted Fever Group Rickettsiosis", "spotted fever rickettsiae disease", "spotted fever Group Rickettsioses", "spotted fever Group rickettsiosis", "Spotted Fever Group Rickettsioses", "Spotted fever group rickettsial disease", "spotted fever group rickettsial disease", "Spotted fever [tick-borne rickettsioses]", "Spotted fever group rickettsial disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spotted fever", "shortest_name_length": 11}
{"curie": "UMLS:C0268108", "names": ["gout chronic", "Chronic gout", "chronic gout", "GOUTY ARTHRITIS CHRONIC", "Chronic gouty arthritis", "chronic gout (diagnosis)", "chronic gouty arthropathy", "gouty arthropathy chronic", "Chronic arthritis due to gout", "chronic gouty arthropathy (diagnosis)", "Chronic arthritis due to gout (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic gouty arthritis", "shortest_name_length": 12}
{"curie": "MONDO:0100277", "names": ["disorder of peroxisomal alpha oxidation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of peroxisomal alpha oxidation", "shortest_name_length": 39}
{"curie": "MONDO:0015924", "names": ["PAH", "PPH", "HPAH", "FPAH", "PVOD/PCH", "Pulmonary hypertension", "Pulmonary Hypertension", "HYPERTENSION PULMONARY", "PULMONARY HYPERTENSION", "pulmonary hypertension", "Hypertension pulmonary", "Hypertension, Pulmonary", "Pulmonary hypertensions", "pulmonary; hypertension", "hypertension; pulmonary", "Hypertension, pulmonary", "Pulmonary hypertension NOS", "Pulmonary hypertension, NOS", "PHT - Pulmonary hypertension", "Hypertension;pulmonar;primary", "Pulmonary artery hypertension", "PULMONARY HYPERTENSION PRIMARY", "hypertension primary pulmonary", "Primary Pulmonary Hypertension", "Hypertension;pulmonar;idiopath", "pulmonary primary hypertension", "Pulmonary hypertension primary", "Primary pulmonary hypertension", "primary pulmonary hypertension", "Pulmonary arterial hypertension", "familial pulmonary hypertension", "pulmonary arterial hypertension", "pulmonary hypertension disorder", "Pulmonary hypertension, primary", "Pulmonary Arterial Hypertension", "Hypertension, pulmonary, primary", "Hypertension, Pulmonary Arterial", "HYPERTENSION, PULMONARY, PRIMARY", "lesser circulation; hypertension", "Essential pulmonary hypertension", "Arterial Hypertension, Pulmonary", "hypertension; lesser circulation", "Idiopathic pulmonary hypertension", "idiopathic pulmonary hypertension", "Pulmonary hypertension (disorder)", "Pulmonary hypertension, essential", "pulmonary hypertension (diagnosis)", "Pulmonary hypertension, idiopathic", "hypertension caused by lung disease", "PPHT - Primary pulmonary hypertension", "Familial Primary Pulmonary Hypertension", "pulmonary hypertension primary familial", "Hypertensive pulmonary arterial disease", "Hypertensive pulmonary vascular disease", "Pulmonary hypertensive arterial disease", "Familial primary pulmonary hypertension", "Familial pulmonary arterial hypertension", "Heritable Pulmonary Arterial Hypertension", "Heritable pulmonary arterial hypertension", "Hereditary pulmonary arterial hypertension", "primary pulmonary hypertension (diagnosis)", "Pulmonary arterial hypertension (diagnosis)", "familial pulmonary hypertension (diagnosis)", "pulmonary hypertension precapillary arterial", "Familial primary pulmonary hypertension (disorder)", "Pulmonary hypertensive arterial disease (disorder)", "Increased blood pressure in blood vessels of lungs", "Heritable pulmonary arterial hypertension (disorder)", "PAH with overt features of venous/capillaries involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary arterial hypertension", "shortest_name_length": 3}
{"curie": "MONDO:0009492", "names": ["SCOTD", "SCOT DEFICIENCY", "Scot deficiency", "SCOT deficiency", "OXCT1 deficiency", "Thioacyl transferase deficiency", "Ketoacidosis due to SCOT deficiency", "ketoacidosis due to Scot deficiency", "KETOACIDOSIS DUE TO SCOT DEFICIENCY", "3-oxoacid CoA transferase deficiency", "3-Ketoacid CoA transferase deficiency", "Succinyl-Coa 3-Oxoacid Transferase Deficiency", "Succinyl-CoA 3-ketoacid transferase deficiency", "Succinyl-Coa:Acetoacetate Transferase Deficiency", "succinyl-CoA acetoacetate transferase deficiency", "Succinyl-CoA acetoacetate transferase deficiency", "succinyl-Coa:acetoacetate transferase deficiency", "SUCCINYL-CoA:ACETOACETATE TRANSFERASE DEFICIENCY", "succinyl-CoA:3-oxoacid-CoA transferase deficiency", "SUCCINYL-CoA:3-OXOACID-CoA TRANSFERASE DEFICIENCY", "succinyl-CoA:3-oxoacid CoA transferase deficiency", "Succinyl-CoA:3-oxoacid CoA transferase deficiency", "Succinyl CoA:3-oxoacid CoA transferase deficiency", "Succinyl-Coa:3-Ketoacid Coa Transferase Deficiency", "SUCCINYL-CoA:3-KETOACID CoA-TRANSFERASE DEFICIENCY", "Succinyl-CoA:3-ketoacid CoA transferase deficiency", "succinyl-Coa:3-ketoacid Coa-transferase deficiency", "succinyl-CoA:3-ketoacid CoA transferase deficiency", "Succinyl-Coa:3-Ketoacid Coa-Transferase Deficiency", "Succinyl-coenzyme A acetoacetate transferase deficiency", "Succinyl-coenzyme A acetoacetate transferase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "succinyl-CoA:3-ketoacid CoA transferase deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0016430", "names": ["Baló", "Balo disease", "balo's disease", "Balo's disease", "sclerosis; Baló", "Baló; sclerosis", "Marburg variant", "concentric sclerosis", "Concentric sclerosis", "concentric; sclerosis", "sclerosis; concentric", "Concentric demyelination", "concentric demyelination", "balo concentric sclerosis", "Balo concentric sclerosis", "Balo Concentric Sclerosis", "Baló concentric sclerosis", "Balos concentric sclerosis", "Concentric Sclerosis, Balo", "balo's concentric sclerosis", "Concentric sclerosis [Balo]", "Balo's Concentric Sclerosis", "Balo's concentric sclerosis", "balos concentrics sclerosis", "Scleroses, Balo's Concentric", "Concentric Sclerosis, Balo's", "Tumefactive multiple sclerosis", "Encephalitis periaxialis, Balo's", "Balo concentric sclerosis (disorder)", "Encephalitis periaxialis concentrica", "encephalitis periaxialis concentrica", "encephalitis; periaxialis concentrica", "Encephalitis periaxialis, concentrica", "periaxialis; encephalitis, concentrica", "diffuse cerebral sclerosis of Schilder", "encephalitis; periaxialis, concentrica", "Balo's concentric sclerosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Balo concentric sclerosis", "shortest_name_length": 4}
{"curie": "MONDO:0011972", "names": ["OHSS", "Secondary Meig's syndrome", "secondary Meig's syndrome", "Ovarian hyperstimulation syndrome", "OVARIAN HYPERSTIMULATION SYNDROME", "ovarian hyperstimulation syndrome", "Ovarian Hyperstimulation Syndrome", "Hyperstimulation Syndrome, Ovarian", "Ovarian Hyperstimulation Syndromes", "Hyperstimulation Syndromes, Ovarian", "Ovarian hyperstimulation syndrome (disorder)", "ovarian hyperstimulation syndrome (diagnosis)", "ovarian hyperstimulation syndrome, familial gestational spontaneous", "OVARIAN HYPERSTIMULATION SYNDROME, FAMILIAL GESTATIONAL SPONTANEOUS", "Ovarian Hyperstimulation Syndrome, Familial Gestational Spontaneous"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian hyperstimulation syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0024265", "names": ["Drs", "DURS1", "Duane anomaly", "Duane syndrome", "retraction syndrome", "Duane syndrome type 1", "1 duanes syndrome type", "Duane syndrome, type 1", "type I Duane's syndrome", "duane's syndrome type 1", "Esotropic Duane syndrome", "Duane's syndrome, type 1", "Duane syndrome, type one", "Esotropic Duane's syndrome", "Duane retraction syndrome 1", "Duane Retraction Syndrome 1", "DUANE RETRACTION SYNDROME 1", "Type 1 Duane Retraction Syndrome", "Duane Retraction Syndrome, Type 1", "type I Duane's syndrome (diagnosis)", "Duane's syndrome, type 1 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Duane syndrome type 1", "shortest_name_length": 3}
{"curie": "MONDO:0001236", "names": ["appendix tumor", "Appendix Tumor", "appendix tumors", "tumor of appendix", "appendix neoplasm", "Tumor of appendix", "Tumor of Appendix", "Appendix Neoplasm", "Appendiceal tumor", "Tumour of appendix", "Appendiceal tumour", "appendix neoplasms", "neoplasm of appendix", "Neoplasm of Appendix", "Appendiceal Neoplasm", "appendiceal neoplasm", "Neoplasm of appendix", "Appendiceal Neoplasms", "tumor of the appendix", "appendiceal neoplasms", "Neoplasm, Appendiceal", "Tumor of the Appendix", "Neoplasms, Appendiceal", "Neoplasm of the Appendix", "vermiform appendix tumor", "neoplasm of the appendix", "tumor of vermiform appendix", "vermiform appendix neoplasm", "neoplasm of vermiform appendix", "Neoplasm of appendix (disorder)", "neoplasm of appendix (diagnosis)", "vermiform appendix neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "appendiceal neoplasm", "shortest_name_length": 14}
{"curie": "MONDO:0004875", "names": ["CX", "Xanthogranulomatous cholecystitis", "xanthogranulomatous cholecystitis", "Xanthogranulomatous Cholecystitis", "Xanthogranulomatous cholecystitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "xanthogranulomatous cholecystitis", "shortest_name_length": 2}
{"curie": "UMLS:C2981395", "names": ["Stage II Appendix Carcinoid Tumor", "Stage II Appendix Neuroendocrine Tumor", "Stage II Appendix Carcinoid Tumor AJCC v7", "Stage II Appendix Neuroendocrine Tumor AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Appendix Neuroendocrine Tumor AJCC v7", "shortest_name_length": 33}
{"curie": "UMLS:C1328411", "names": ["Post procedural hematoma", "Post procedural haematoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post procedural hematoma", "shortest_name_length": 24}
{"curie": "MONDO:0000927", "names": ["asymptomatic neurosyphilis", "Asymptomatic neurosyphilis", "neurosyphilis; asymptomatic", "Neurosyphilis, Asymptomatic", "asymptomatic; neurosyphilis", "Asymptomatic neurosyphilis (disorder)", "asymptomatic neurosyphilis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "asymptomatic neurosyphilis", "shortest_name_length": 26}
{"curie": "MONDO:0000513", "names": ["bone ameloblastoma", "bone tissue ameloblastoma", "ameloblastoma of bone tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bone ameloblastoma", "shortest_name_length": 18}
{"curie": "UMLS:C2981635", "names": ["Stage IIIA Hilar Cholangiocarcinoma", "Stage IIIA Hilar Cholangiocarcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Hilar Cholangiocarcinoma AJCC v7", "shortest_name_length": 35}
{"curie": "UMLS:C1880101", "names": ["clear cell type neoplasm", "Clear Cell Malignant Neoplasm", "malignant clear cell neoplasm", "clear cell type neoplasm (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "clear cell type neoplasm", "shortest_name_length": 24}
{"curie": "MONDO:0005675", "names": ["Border disease", "border disease", "Border Disease", "Border Diseases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "border disease", "shortest_name_length": 14}
{"curie": "MONDO:0013587", "names": ["LDHBD", "LDH deficiency B", "LDH-H subunit deficiency", "Lactate dehydrogenase B deficiency", "LACTATE DEHYDROGENASE B DEFICIENCY", "lactate dehydrogenase-B deficiency", "Lactate Dehydrogenase B Deficiency", "lactate dehydrogenase B deficiency", "Reduced lactate dehydrogenase B level", "lactate dehydrogenase deficiency type B", "GSD due to lactate dehydrogenase H-subunit deficiency", "Glycogenosis due to lactate dehydrogenase H-subunit deficiency", "glycogenosis due to lactate dehydrogenase H-subunit deficiency", "glycogen storage disease due to lactate dehydrogenase H-subunit deficiency", "Glycogen storage disease due to lactate dehydrogenase H-subunit deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease due to lactate dehydrogenase H-subunit deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C5418571", "names": ["Resectable Skin Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Skin Carcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0008511", "names": ["Vessel's syndrome", "vessel’s syndrome", "Cushing Symphalangism", "proximal symphalangism", "Proximal symphalangism", "SYMPHALANGISM, PROXIMAL", "Cushing's symphalangism", "Symphalangism, Proximal", "Symphalangism Cushing type", "Symphalangism, Cushing type", "symphalangism, Cushing type", "proximal symphalangism (disease)", "Strasburger-Hawkins-Eldridge syndrome", "Hereditary absence of proximal interphalangeal joints", "hereditary absence of proximal interphalangeal joints", "Strasburger-Hawkins-Eldridge-Hargrave-McKusick syndrome", "Proximal interphalangeal joint symphalangism Cushing type", "Hereditary Absence of the Proximal Interphalangeal Joints", "hereditary absence of the proximal interphalangeal joints", "Proximal interphalangeal joint symphalangism Cushing type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "proximal symphalangism", "shortest_name_length": 17}
{"curie": "MONDO:0017403", "names": ["familial isolated arrhythmogenic ventricular dysplasia, classic form", "familial isolated arrhythmogenic ventricular cardiomyopathy, classic form", "familial isolated arrhythmogenic ventricular dysplasia, right dominant form", "familial isolated arrhythmogenic ventricular cardiomyopathy, right dominant form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial isolated arrhythmogenic ventricular dysplasia, right dominant form", "shortest_name_length": 68}
{"curie": "MONDO:0009633", "names": ["MSPKA", "microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma", "MICROSPHEROPHAKIA AND/OR MEGALOCORNEA, WITH ECTOPIA LENTIS AND WITH OR WITHOUT SECONDARY GLAUCOMA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma", "shortest_name_length": 5}
{"curie": "MONDO:0022468", "names": ["TAP 2 deficiency", "antigen-peptide-transporter 2 deficiency", "antigen processing (TAP) deficiency syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "antigen-peptide-transporter 2 deficiency", "shortest_name_length": 16}
{"curie": "EFO:0009959", "names": ["diverticular disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diverticular disease", "shortest_name_length": 20}
{"curie": "UMLS:C0859034", "names": ["Acute Uric Acid Nephropathy", "Uric acid nephropathy acute"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uric acid nephropathy acute", "shortest_name_length": 27}
{"curie": "UMLS:C0151464", "names": ["INJECTION SITE ABSCESS", "Injection site abscess", "Abscess injection site", "ABSCESS INJECTION SITE", "injection site disorder abscess", "Injection site abscess (disorder)", "Injection site abscess (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site abscess", "shortest_name_length": 22}
{"curie": "UMLS:C4087120", "names": ["ICU acquired weakness", "Intensive care unit acquired weakness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intensive care unit acquired weakness", "shortest_name_length": 21}
{"curie": "MONDO:0013690", "names": ["PTHSL2", "Pitt-Hopkins-like syndrome 2", "PITT-HOPKINS-LIKE SYNDROME 2", "NRXN1 Pitt-Hopkins-like syndrome", "Pitt-Hopkins-like syndrome type 2", "Pitt-Hopkins-like syndrome caused by mutation in NRXN1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pitt-Hopkins-like syndrome 2", "shortest_name_length": 6}
{"curie": "UMLS:C4521714", "names": ["IVB", "Stage IVB Esophageal Adenocarcinoma", "Pathologic Stage IVB Esophageal Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IVB Esophageal Adenocarcinoma AJCC v8", "shortest_name_length": 3}
{"curie": "MONDO:0013466", "names": ["OFC13", "OROFACIAL CLEFT 13", "orofacial cleft 13"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orofacial cleft 13", "shortest_name_length": 5}
{"curie": "MONDO:0042902", "names": ["Say Carpenter syndrome", "Say-Carpenter syndrome", "metaphyseal dysplasia hypertelorism hypospadias"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Say-Carpenter syndrome", "shortest_name_length": 22}
{"curie": "MONDO:0004762", "names": ["Taylor syndrome", "Pelvic congestion", "PELVIC CONGESTION", "Taylor's syndrome", "taylor's syndrome", "pelvic congestion", "Pelvic pain syndrome", "pelvic pain syndrome", "Pelvic pressure syndrome", "congestive pelvic syndrome", "congestion pelvic syndrome", "Pelvic congestive syndrome", "pelvic congestion syndrome", "pelvic congestive syndrome", "Pelvic congestion syndrome", "PPS - Pelvic pain syndrome", "Congestion-fibrosis syndrome", "congestion-fibrosis syndrome", "congestion fibrosis syndrome", "syndrome; congestion-fibrosis", "congestion; fibrosis syndrome", "Pelvic congestion syndrome (disorder)", "pelvic congestion syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Taylor syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0005047", "names": ["Sterile", "sterile", "STERILITY", "Sterility", "Infertile", "sterility", "infertile", "Infertility", "infertility", "Not fertile", "INFERTILITY", "Sterility, NOS", "Infertility NOS", "Infertility, NOS", "fertility issues", "Fertility issues", "Fertility Disorder", "unable to conceive", "Infertile (finding)", "Fertility Disorders", "Sterility (finding)", "disorders fertility", "get pregnant unable", "FERTILITY DISORDERS", "fertility disorders", "Unable (to);conceive", "infertility disorder", "inability to conceive", "infertility (symptom)", "Difficulty conceiving", "unable to get pregnant", "Reproductive Sterility", "Sterility, Reproductive", "Unable (to);get pregnant", "unable (to) get pregnant", "Cannot achieve a pregnancy", "inability to conceive (symptom)", "inability to conceive (infertility)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infertility disorder", "shortest_name_length": 7}
{"curie": "MONDO:0010918", "names": ["IGE", "EIG", "EIG1", "epilepsy generalized primary", "primary generalized epilepsy", "Primary generalized epilepsy", "Primary generalised epilepsy", "IDIOPATHIC GENERALIZED EPILEPSY", "generalized idiopathic epilepsy", "Idiopathic generalised epilepsy", "epilepsy generalized idiopathic", "idiopathic generalized epilepsy", "Idiopathic Generalized Epilepsy", "Idiopathic generalized epilepsy", "Epilepsy, Idiopathic Generalized", "EPILEPSY, IDIOPATHIC GENERALIZED", "epilepsies generalised idiopathic", "epilepsy; generalized, idiopathic", "epilepsy; idiopathic, generalized", "generalized; epileptic, idiopathic", "Idiopathic generalized epilepsy, NOS", "Idiopathic generalized epilepsy (disorder)", "epilepsy; syndrome, generalized, idiopathic", "generalized idiopathic epilepsy (diagnosis)", "syndrome; epileptic, generalized, idiopathic", "epilepsy, idiopathic generalized, susceptibility to, 1", "Generalized idiopathic epilepsy and epileptic syndromes", "Generalised idiopathic epilepsy and epileptic syndromes", "Generalized idiopathic epilepsy and epileptic syndromes NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, idiopathic generalized, susceptibility to, 1", "shortest_name_length": 3}
{"curie": "UMLS:C1334053", "names": ["HPVA Cervical Adenocarcinoma", "HPV-Related Endocervical Adenocarcinoma", "Human Papillomavirus-Related Cervical Adenocarcinoma", "Human Papillomavirus-Associated Cervical Adenocarcinoma", "Human Papillomavirus-Related Endocervical Adenocarcinoma", "Human Papilloma Virus Related Endocervical Adenocarcinoma", "Human Papilloma Virus-Related Endocervical Adenocarcinoma", "Human Papillomavirus- Associated Endocervical Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Human Papillomavirus-Related Cervical Adenocarcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0032610", "names": ["MC1DN5", "nuclear type mitochondrial complex I deficiency 5", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 5", "mitochondrial complex 1 deficiency, nuclear type 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 5", "shortest_name_length": 6}
{"curie": "MONDO:0010676", "names": ["Muscular Dystrophy, Hemizygous Lethal Type", "muscular dystrophy, Hemizygous lethal type", "MUSCULAR DYSTROPHY, HEMIZYGOUS LETHAL TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy, Hemizygous lethal type", "shortest_name_length": 42}
{"curie": "MONDO:0007865", "names": ["Garrod", "knuckle pad", "Knuckle pad", "knuckle pads", "Knuckle pads", "KNUCKLE PADS", "Knuckle Pads", "Garrod's pads", "garrod's pads", "Knuckle pads (disorder)", "Garrod's or knuckle pads", "pad, knuckle or Garrod's", "Knuckle pads (diagnosis)", "Knuckle pads on dorsal aspect of finger joints", "fibromatoses of muscle, ligament, and fascia knuckle pads"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "knuckle pads", "shortest_name_length": 6}
{"curie": "MONDO:0004608", "names": ["Oropharynx Cancer", "Oropharnyx Cancer", "cancer oropharynx", "oropharynx cancer", "Oropharnyx Cancers", "Cancer, Oropharynx", "Oropharynx Cancers", "Cancers, Oropharynx", "Cancer of Oropharnyx", "cancer oropharyngeal", "Oropharyngeal Cancer", "oropharyngeal cancer", "Oropharyngeal cancer", "Cancer of oropharynx", "Cancer of Oropharynx", "cancer of oropharynx", "Oropharynx Carcinoma", "Cancer, Oropharyngeal", "Oropharyngeal Cancers", "Cancers, Oropharyngeal", "Oropharyngeal Neoplasms", "Carcinoma of Oropharynx", "Oropharyngeal Carcinoma", "Oropharyngeal carcinoma", "carcinoma of oropharynx", "oropharyngeal carcinoma", "cancer of the oropharynx", "Cancer of the Oropharynx", "CA - Cancer of oropharynx", "Carcinoma of the Oropharynx", "Malignant Oropharyngeal Tumor", "malignant Oropharyngeal tumor", "Malignant tumor of oropharynx", "Malignant Tumor of Oropharynx", "malignant oropharyngeal tumor", "malignant oropharynx neoplasm", "malignant tumor of oropharynx", "Malignant tumor of mesopharynx", "Malignant tumour of oropharynx", "OROPHARYNGEAL CANCER MALIGNANT", "Malignant tumour of mesopharynx", "malignant tumour of mesopharynx", "malignant neoplasm of oropharynx", "Malignant Oropharyngeal Neoplasm", "malignant oropharyngeal neoplasm", "Malignant Neoplasm of Oropharynx", "Malignant neoplasm of oropharynx", "Malignant Tumor of the Oropharynx", "malignant tumor of the oropharynx", "carcinoma of oropharynx (diagnosis)", "malignant neoplasm of the oropharynx", "Cancer of lateral wall of oropharynx", "Malignant Neoplasm of the Oropharynx", "Malignant neoplasm of oropharynx, NOS", "Malignant tumor of oropharynx (disorder)", "malignant neoplasm of oropharynx (diagnosis)", "Malignant neoplasm of oropharynx, unspecified", "malignant tumor of lateral wall of oropharynx", "malignant tumor of posterior wall of oropharynx", "Malignant tumor of posterior wall of oropharynx", "Malignant tumour of posterior wall of oropharynx", "malignant neoplasm of lateral wall of oropharynx", "Malignant neoplasm of lateral wall of oropharynx", "Malignant neoplasm of oropharynx, unspecified site", "Malignant neoplasm of posterior wall of oropharynx", "malignant neoplasm of posterior wall of oropharynx", "Malignant neoplasm of junctional region of oropharynx", "malignant neoplasm of junctional region of oropharynx", "oropharyngeal neoplasm lateral wall, malignant primary", "primary malignant neoplasm of lateral wall of oropharynx", "Primary malignant neoplasm of lateral wall of oropharynx", "Malignant tumor of posterior wall of oropharynx (disorder)", "Malignant neoplasm of lateral wall of oropharynx (disorder)", "malignant neoplasm of lateral wall of oropharynx (diagnosis)", "malignant neoplasm of posterior wall of oropharynx (diagnosis)", "Primary malignant neoplasm of lateral wall of oropharynx (disorder)", "Primary malignant neoplasm of lateral wall of oropharynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oropharynx cancer", "shortest_name_length": 17}
{"curie": "MONDO:0014778", "names": ["LAMSHF", "LAMB-SHAFFER SYNDROME", "Lamb-Shaffer syndrome", "Lamb Shaffer syndrome", "Lamb-Shaffer syndrome; LAMSHF", "SOX5 haploinsufficiency syndrome", "Lamb Shaffer syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lamb-Shaffer syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0015497", "names": ["hypoglossia/aglossia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypoglossia/aglossia", "shortest_name_length": 20}
{"curie": "UMLS:C4524894", "names": ["Anal Carcinoma by AJCC v6 and v7 Stage", "Anal Canal Cancer by AJCC v6 and v7 Stage", "Anal Canal Carcinoma by AJCC v6 and v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anal Canal Cancer by AJCC v6 and v7 Stage", "shortest_name_length": 38}
{"curie": "MONDO:0003429", "names": ["Functioning PitNET/Adenoma", "Secreting pituitary adenoma", "Secretory Pituitary Adenoma", "secretory pituitary adenoma", "secreting pituitary adenoma", "Functioning pituitary adenoma", "Functioning Pituitary Adenoma", "functioning pituitary adenoma", "secretory adenoma of pituitary", "Secretory adenoma of pituitary", "pituitary adenoma, functioning", "Secretory Adenoma of Pituitary", "Functioning Adenoma of Pituitary", "functioning adenoma of pituitary", "secretory pituitary gland adenoma", "Secretory Pituitary Gland Adenoma", "Secretory Adenoma of the Pituitary", "secretory adenoma of the pituitary", "endocrine active pituitary adenoma", "Endocrine active pituitary adenoma", "Functioning Pituitary Gland Adenoma", "functioning pituitary gland adenoma", "Functioning Adenoma of the Pituitary", "secretory adenoma of pituitary gland", "Secretory Adenoma of Pituitary Gland", "functioning adenoma of the pituitary", "functioning adenoma of pituitary gland", "Functioning Adenoma of Pituitary Gland", "secretory adenoma of the pituitary gland", "Secretory adenoma of the Pituitary gland", "Secretory Adenoma of the Pituitary Gland", "functioning adenoma of the pituitary gland", "Functioning Pituitary Neuroendocrine Tumor", "Functioning Adenoma of the Pituitary Gland", "functioning pituitary gland adenoma (benign)", "Functioning Pituitary Neuroendocrine Tumor/Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "functioning pituitary gland adenoma", "shortest_name_length": 26}
{"curie": "UMLS:C1319200", "names": ["postoperative confusion", "Postoperative confusion", "Confusion postoperative", "Post-operative confusion", "Post-operative confusion (disorder)", "postoperative confusion (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postoperative confusion", "shortest_name_length": 23}
{"curie": "MONDO:0007304", "names": ["cervical vertebral Bridge", "CERVICAL VERTEBRAL BRIDGE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical vertebral Bridge", "shortest_name_length": 25}
{"curie": "MONDO:0021163", "names": ["renal tumor", "Renal Tumor", "Renal tumor", "kidney tumor", "renal tumour", "Renal tumors", "Renal Tumors", "Renal tumour", "Kidney Tumor", "Kidney tumor", "renal tumors", "Kidney cancer", "renal tumours", "Kidney tumour", "Renal tumours", "kidney tumors", "kidney tumour", "Renal Neoplasm", "kidney tumours", "renal neoplasm", "Renal neoplasm", "kidney neoplasm", "Neoplasia renal", "Neoplasm, Renal", "NEOPLASIA RENAL", "Renal neoplasia", "renal neoplasms", "RENAL NEOPLASIA", "Renal neoplasms", "tumor of kidney", "Kidney Neoplasm", "Tumor of kidney", "Renal Neoplasms", "Tumor of Kidney", "Kidneys--Tumors", "Kidney Neoplasms", "Tumour of kidney", "Neoplasm, Kidney", "kidney neoplasms", "Neoplasms, Renal", "Neoplasms, Kidney", "Renal neoplasm NOS", "Neoplasm of kidney", "neoplasm of kidney", "Neoplasm of Kidney", "Tumor of the Kidney", "tumor of the kidney", "Tumors of the kidney", "neoplasm of the kidney", "Neoplasm of the Kidney", "Neoplasia of the kidneys", "kidney neoplasm (disease)", "Neoplasm of kidney (disorder)", "neoplasm of kidney (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kidney neoplasm", "shortest_name_length": 11}
{"curie": "UMLS:C0085996", "names": ["Child Development Deviation", "Development Deviation, Child", "Child development deviations", "Child Development Deviations", "Deviation, Child Development", "Development Deviations, Child"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Child Development Deviations", "shortest_name_length": 27}
{"curie": "UMLS:C4525691", "names": ["Appendix Neuroendocrine Tumor by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Appendix Neuroendocrine Tumor by AJCC v7 Stage", "shortest_name_length": 46}
{"curie": "MONDO:0002465", "names": ["bronchiolitis", "Bronchiolitis", "BRONCHIOLITIS", "Bronchiolitides", "Wheezy Bronchitis", "RSV bronchiolitis", "wheezy bronchitis", "Bronchiolitis, NOS", "viral bronchiolitis", "bronchiolitis (disease)", "Bronchiolitis (disorder)", "bronchiolitis (diagnosis)", "Respiratory bronchiolitis", "Inflammation of the bronchioles"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bronchiolitis", "shortest_name_length": 13}
{"curie": "UMLS:C5239286", "names": ["Cutaneous Histiocytic and Dendritic Cell Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous Histiocytic and Dendritic Cell Neoplasm", "shortest_name_length": 49}
{"curie": "MONDO:0021418", "names": ["polyp; ethmoid", "ethmoid; polyp", "Ethmoidal polyp", "Ethmoidal Polyp", "ethmoidal polyp", "ethmoidal polyps", "ethmoid sinus polyp", "Ethmoid Sinus Polyp", "Ethmoidal Sinus Polyp", "ethmoidal sinus polyp", "polyp of ethmoid sinus", "Polyp of Ethmoid Sinus", "Polyp of Ethmoidal Sinus", "Polyp of ethmoidal sinus", "polyp of ethmoidal sinus", "Ethmoidal polyp of sinus", "Polyp of sinus, ethmoidal", "Polyp of the Ethmoid Sinus", "polyp of the ethmoid sinus", "Polyp of the Ethmoidal Sinus", "polyp of the ethmoidal sinus", "Polyp of ethmoidal sinus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyp of ethmoidal sinus", "shortest_name_length": 14}
{"curie": "MONDO:0016303", "names": ["TGA with cardiac malformation", "congenitally uncorrected transposition of the great vessels with cardiac malformation", "congenitally uncorrected transposition of the great arteries with cardiac malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenitally uncorrected transposition of the great arteries with cardiac malformation", "shortest_name_length": 29}
{"curie": "MONDO:0004051", "names": ["aleukemic monocytic leukemia cutis", "Aleukemic Monocytic Leukemia Cutis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aleukemic monocytic leukemia cutis", "shortest_name_length": 34}
{"curie": "MONDO:0020305", "names": ["isochromosomy Yq"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isochromosomy Yq", "shortest_name_length": 16}
{"curie": "MONDO:0003857", "names": ["CNS Solitary Fibrous Tumor, Grade 3", "Adult CNS Solitary Fibrous Tumor, Grade 3", "adult intracranial malignant hemangiopericytoma", "Adult Intracranial Malignant Hemangiopericytoma", "Adult Malignant Intracranial Hemangiopericytoma", "adult malignant intracranial hemangiopericytoma", "malignant adult intracranial hemangiopericytoma", "Malignant Adult Intracranial Hemangiopericytoma", "Adult Intracranial Anaplastic Hemangiopericytoma", "adult intracranial anaplastic hemangiopericytoma", "Central Nervous System Malignant Hemangiopericytoma", "Central Nervous System Anaplastic Hemangiopericytoma", "CNS Solitary Fibrous Tumor/Hemangiopericytoma, Grade 3", "Central Nervous System Solitary Fibrous Tumor, Grade 3", "Solitary fibrous tumor/hemangiopericytoma Grade 3 (CNS)", "Adult Central Nervous System Solitary Fibrous Tumor, Grade 3", "Adult Intracranial Solitary Fibrous Tumor/Hemangiopericytoma, Grade 3", "adult intracranial solitary fibrous tumor/hemangiopericytoma, grade 3", "Central Nervous System Solitary Fibrous Tumor/Hemangiopericytoma, Grade 3", "central nervous system solitary fibrous tumor/hemangiopericytoma, grade 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult intracranial malignant hemangiopericytoma", "shortest_name_length": 35}
{"curie": "MONDO:0001962", "names": ["Glucagon secretion disorder", "glucagon; secretion abnormal", "secretion; glucagon abnormal", "abnormal; glucagon secretion", "glucagon secretion abnormality", "Glucagon secretion abnormality", "Glucagon secretion disorder NOS", "abnormality of glucagon secretion", "Abnormality of glucagon secretion", "Abnormality of secretion of glucagon", "Abnormality of secretion of glucagon, NOS", "Abnormality of secretion of glucagon (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "abnormality of glucagon secretion", "shortest_name_length": 27}
{"curie": "UMLS:C0266808", "names": ["chronic gi bleeding", "Chronic GI bleeding", "Chronic GI hemorrhage", "Chronic GI haemorrhage", "GASTROINTESTINAL BLEED CHRONIC", "Chronic gastrointestinal bleeding", "bleeding chronic gastrointestinal", "Chronic gastrointestinal hemorrhage", "Chronic gastrointestinal haemorrhage", "Chronic gastrointestinal hemorrhage (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic gastrointestinal hemorrhage", "shortest_name_length": 19}
{"curie": "UMLS:C4683750", "names": ["Stage IVA2 Mycosis Fungoides and Sezary Syndrome AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA2 Mycosis Fungoides and Sezary Syndrome AJCC v8", "shortest_name_length": 56}
{"curie": "MONDO:0800026", "names": ["OHD", "CCHS", "CCHS1", "ondine curse", "Ondine curse", "ONDINES CURSE", "ondines curse", "Ondine's curse", "ondine's curse", "curse, Ondine's", "Ondine syndrome", "ondine syndrome", "Haddad syndrome", "HADDAD SYNDROME", "Haddad Syndrome", "Ondine curse (formerly)", "congenital Ondine curse", "Congenital Ondine curse", "Ondine curse, congenital", "Ondine Curse, Congenital", "ONDINE CURSE, CONGENITAL", "Ondine's curse (formerly)", "neurogenic hypoventilation", "Ondine's curse (diagnosis)", "Haddad syndrome (disorder)", "NEUROGENIC HYPOVENTILATION", "Ondine-Hirschsprung disease", "Ondine Hirschsprung disease", "ONDINE-HIRSCHSPRUNG DISEASE", "Ondine-Hirschsprung Disease", "HYPOVENTILATION, IDIOPATHIC", "Ondine-Hirschsprung syndrome", "Ondine Hirschsprung syndrome", "Cchs With Hirschsprung Disease", "CCHS WITH HIRSCHSPRUNG DISEASE", "CCHS with Hirschsprung disease", "Central-alveolar hypoventilation", "Central Hypoventilation Syndrome", "Primary alveolar hypoventilation", "primary alveolar hypoventilation", "Sleep-related respiratory failure", "ALVEOLAR HYPOVENTILATION, PRIMARY", "Congenital Central Hypoventilation", "Congenital central hypoventilation", "congenital central hypoventilation", "Congenital pulmonary hypoventilation", "Hypothalamic hypoventilation syndrome", "Congenital failure of autonomic control", "congenital failure of autonomic control", "autonomic control, congenital failure of", "AUTONOMIC CONTROL, CONGENITAL FAILURE OF", "Autonomic Control, Congenital Failure of", "CCHS - Congenital central hypoventilation", "Primary alveolar hypoventilation (finding)", "congenital central hypoventilation syndrome", "central congenital hypoventilation syndrome", "Congenital Central Hypoventilation Syndrome", "Congenital central hypoventilation syndrome", "central hypoventilation syndrome, congenital", "Central Hypoventilation Syndrome, Congenital", "Sleep-related respiratory failure (disorder)", "Congenital central hypoventilation (disorder)", "CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL, 1", "congenital central alveolar hypoventilation syndrome", "Congenital central alveolar hypoventilation syndrome", "Idiopathic congenital central alveolar hypoventilation", "idiopathic congenital central alveolar hypoventilation", "Congenital central alveolar hypoventilation-Hirschsprung disease syndrome", "Congenital central alveolar hypoventilation with Hirschsprung disease syndrome", "central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease", "shortest_name_length": 3}
{"curie": "MONDO:0012004", "names": ["PRTC", "Parathyroid Cancer", "parathyroid cancer", "Parathyroid cancer", "Cancer, Parathyroid", "Parathyroid Cancers", "Cancers, Parathyroid", "parathyroid neoplasm", "Parathyroid Carcinoma", "carcinoma parathyroid", "Parathyroid carcinoma", "parathyroid carcinoma", "Cancer of Parathyroid", "PARATHYROID CARCINOMA", "Parathyroid carcinomas", "Carcinoma, Parathyroid", "PARATHYROID, CARCINOMA", "Parathyroid Carcinomas", "Carcinomas, Parathyroid", "Parathyroid cancer, NOS", "Carcinoma of Parathyroid", "parathyroid gland cancer", "Parathyroid Gland Cancer", "carcinoma of parathyroid", "Cancer of the Parathyroid", "cancer of the parathyroid", "Parathyroid Adenocarcinoma", "parathyroid gland neoplasm", "Parathyroid gland neoplasm", "parathyroid adenocarcinoma", "PARATHYROID, ADENOCARCINOMA", "Parathyroid Gland Carcinoma", "cancer of parathyroid gland", "parathyroid gland carcinoma", "Cancer of Parathyroid Gland", "carcinoma of the parathyroid", "Carcinoma of the Parathyroid", "Adenocarcinoma of Parathyroid", "adenocarcinoma of parathyroid", "neoplasm of parathyroid gland", "Carcinoma of Parathyroid Gland", "carcinoma of Parathyroid gland", "carcinoma of parathyroid gland", "cancer of the parathyroid gland", "Cancer of the Parathyroid Gland", "Parathyroid carcinoma (disorder)", "parathyroid gland adenocarcinoma", "Parathyroid Gland Adenocarcinoma", "Adenocarcinoma of the Parathyroid", "adenocarcinoma of the parathyroid", "Carcinoma of the Parathyroid Gland", "carcinoma of the parathyroid gland", "PARATHYROID CANCER, ADENOCARCINOMA", "Adenocarcinoma of Parathyroid Gland", "adenocarcinoma of parathyroid gland", "malignant tumor of parathyroid gland", "malignant neoplasm of the parathyroid", "malignant neoplasm of the Parathyroid", "malignant neoplasm of parathyroid gland", "adenocarcinoma of the parathyroid gland", "Adenocarcinoma of the Parathyroid Gland", "CARCINOMA, PARATHYROID GLAND, MALIGNANT", "carcinoma of parathyroid gland (diagnosis)", "adenocarcinoma of parathyroid gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parathyroid gland carcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0013622", "names": ["BDPLT9", "GP IA Deficiency", "GP Ia DEFICIENCY", "GP Ia deficiency", "Glycoprotein IA Deficiency", "GLYCOPROTEIN Ia DEFICIENCY", "glycoprotein Ia deficiency", "platelet-type bleeding disorder 9", "bleeding disorder, platelet-type, 9", "BLEEDING DISORDER, PLATELET-TYPE, 9", "collagen platelet receptor deficiency", "COLLAGEN PLATELET RECEPTOR DEFICIENCY", "ITGA2 inherited bleeding disorder, platelet-type", "Bleeding diathesis due to integrin alpha2-beta1 deficiency", "bleeding diathesis due to integrin alpha2-beta1 deficiency", "inherited bleeding disorder, platelet-type caused by mutation in ITGA2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "platelet-type bleeding disorder 9", "shortest_name_length": 6}
{"curie": "MONDO:0016625", "names": ["acquired deficiency anemia", "rare acquired deficiency anemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired deficiency anemia", "shortest_name_length": 26}
{"curie": "MONDO:0020495", "names": ["PEHOL", "PEHO-Like Syndrome", "PEHO-like syndrome", "PEHO syndrome-like", "peho-like syndrome", "PEHO-LIKE SYNDROME", "Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome", "progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome", "PROGRESSIVE ENCEPHALOPATHY WITH EDEMA, HYPSARRHYTHMIA, AND OPTIC ATROPHY-LIKE SYNDROME", "Progressive encephalopathy with oedema, hypsarrhythmia, and optic atrophy-like syndrome", "PEHOL (progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like) syndrome", "PEHOL (progressive encephalopathy with oedema, hypsarrhythmia, and optic atrophy-like) syndrome", "Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome (disorder)", "Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PEHO-like syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0033809", "names": ["isolated blepharochalasis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated blepharochalasis", "shortest_name_length": 25}
{"curie": "UMLS:C4682695", "names": ["stage IIA penile cancer", "Stage IIA Penile Cancer", "stage IIA penile cancer AJCC v8", "Stage IIA Penile Cancer AJCC v8", "Stage IIA Penile Squamous Cell Carcinoma AJCC v8", "stage IIA penile squamous cell carcinoma AJCC v8", "Stage IIA Squamous Cell Carcinoma of the Penis AJCC v8", "stage IIA squamous cell carcinoma of the penis AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Penile Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "MONDO:0800047", "names": ["MACTHC1", "TUBB1 autosomal dominant macrothrombocytopenia", "macrothrombocytopenia, isolated, 1, autosomal dominant", "MACROTHROMBOCYTOPENIA, ISOLATED, 1, AUTOSOMAL DOMINANT", "autosomal dominant macrothrombocytopenia TUBB1-related", "macrothrombocytopenia, autosomal dominant, TUBB1-related", "Macrothrombocytopenia, Autosomal Dominant, Tubb1-Related", "autosomal dominant macrothrombocytopenia caused by mutation in TUBB1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macrothrombocytopenia, isolated, 1, autosomal dominant", "shortest_name_length": 7}
{"curie": "MONDO:0014880", "names": ["DURS3", "Duane syndrome type 3", "Duane retraction syndrome 3", "MAFB Duane retraction syndrome", "Duane retraction syndrome 3 with or without deafness", "DUANE RETRACTION SYNDROME 3 WITH OR WITHOUT DEAFNESS", "Duane retraction syndrome caused by mutation in MAFB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Duane retraction syndrome 3 with or without deafness", "shortest_name_length": 5}
{"curie": "MONDO:0005655", "names": ["Ascaridiosis", "Ascaridiasis", "ascaridiosis", "Ascaridiases", "ascaridiasis", "Infection by Ascaridia", "infection by Ascaridia", "Infection by Ascaridia, NOS", "Ascaridia infectious disease", "infection caused by Ascaridia", "Infection caused by Ascaridia", "Ascaridia disease or disorder", "Ascaridia caused disease or disorder", "Infection caused by Ascaridia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ascaridiasis", "shortest_name_length": 12}
{"curie": "UMLS:C4526829", "names": ["Bone Cancer by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone Cancer by AJCC v7 Stage", "shortest_name_length": 28}
{"curie": "MONDO:0022655", "names": ["cardiomyopathy hypogonadism metabolic anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiomyopathy hypogonadism metabolic anomalies", "shortest_name_length": 47}
{"curie": "MONDO:0022067", "names": ["Cantu sanchez-corona fragoso syndrome", "Cantu Sanchez-Corona Fragoso syndrome", "severe mental deficiency proportionate dwarfism and delayed sexual maturation", "severe mental deficiency, proportionate dwarfism, and delayed sexual maturation", "Severe mental deficiency, proportionate dwarfism, and delayed sexual maturation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cantu sanchez-corona fragoso syndrome", "shortest_name_length": 37}
{"curie": "UMLS:C2931860", "names": ["Monosomy 5p", "Deletion 5p", "Deletion 5p (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Monosomy 5p", "shortest_name_length": 11}
{"curie": "MONDO:0012519", "names": ["RSTS DELETION SYNDROME", "Rsts deletion syndrome", "16p13.3 deletion syndrome", "RUBINSTEIN-TAYBI DELETION SYNDROME", "Rubinstein-Taybi deletion syndrome", "chromosome 16p13.3 deletion syndrome", "chromosome 16p13.3 deletion syndrome, proximal", "CHROMOSOME 16p13.3 DELETION SYNDROME, PROXIMAL", "Rubinstein-Taybi syndrome due to 16p13.3 microdeletion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rubinstein-Taybi syndrome due to 16p13.3 microdeletion", "shortest_name_length": 22}
{"curie": "MONDO:0009404", "names": ["HMC SYNDROME", "HMC Syndrome", "HMC syndrome", "Bixler syndrome", "Bixler-Christian-Gorlin syndrome", "Bixler Christian Gorlin syndrome", "Hypertelorism-Microtia-Clefting Syndrome", "hypertelorism-microtia-clefting syndrome", "hypertelorism-microtia-clefting (HMC) syndrome", "Hypertelorism-microtia-facial clefting syndrome", "hypertelorism-microtia-facial clefting syndrome", "hypertelorism microtia facial clefting syndrome", "Hypertelorism microtia facial clefting syndrome", "HMC (hypertelorism, microtia, clefting) syndrome", "HYPERTELORISM, MICROTIA, FACIAL CLEFTING SYNDROME", "Hypertelorism, Microtia, Facial Clefting Syndrome", "hypertelorism, microtia, facial clefting syndrome", "Hypertelorism with microtia and facial clefting syndrome", "Hypertelorism with microtia and facial clefting syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertelorism, microtia, facial clefting syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0020157", "names": ["syndromic palpebral coloboma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic palpebral coloboma", "shortest_name_length": 28}
{"curie": "MONDO:0006530", "names": ["CHOLESTEATOMA", "cholesteatoma", "Cholesteatoma", "cholesteatomas", "Cholesteatomas", "Cholesteatoma, NOS", "cholesteatoma (disease)", "Cholesteatoma (disorder)", "Epidermoid cholesteatoma", "cholesteatoma (diagnosis)", "Unspecified cholesteatoma", "Cholesteatoma, unspecified", "congenital cholesteatoma (type)", "primary acquired cholesteatoma (type)", "Cholesteatoma (morphologic abnormality)", "secondary acquired cholesteatoma (type)", "Unspecified cholesteatoma, unspecified ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholesteatoma", "shortest_name_length": 13}
{"curie": "MONDO:0032669", "names": ["DBA19", "DIAMOND-BLACKFAN ANEMIA 19", "Diamond-Blackfan anemia 19", "RPL35-related Diamond-Blackfan anemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diamond-Blackfan anemia 19", "shortest_name_length": 5}
{"curie": "MONDO:0700189", "names": ["Chicken Neoplasm", "chicken neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chicken neoplasm", "shortest_name_length": 16}
{"curie": "UMLS:C0549374", "names": ["Disc lesion lumbar", "Lumbar disc lesion", "LUMBAR DISC LESION", "Lumbar disc lesion (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lumbar disc lesion", "shortest_name_length": 18}
{"curie": "MONDO:0100188", "names": ["combined ApoA-I and ApoC-III deficiency", "ApoA-I and apoC-III deficiency, combined"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined ApoA-I and ApoC-III deficiency", "shortest_name_length": 39}
{"curie": "UMLS:C0392196", "names": ["Injection site hives", "URTICARIA INJECTION SITE", "Urticaria injection site", "Injection site urticaria", "Injection site urticaria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site urticaria", "shortest_name_length": 20}
{"curie": "MONDO:0009757", "names": ["NPC1", "Niemann-Pick disease type D", "Niemann-Pick Disease Type D", "Niemann Pick Disease Type D", "Niemann-Pick Type D Disease", "Niemann Pick Type D Disease", "Niemann pick disease type D", "Niemann-Pick disease, type D", "Niemann-Pick disease, type C", "Niemann Pick Disease, Type D", "type C1 Niemann-Pick disease", "Niemann-Pick disease type C1", "Niemann-Pick Disease, Type D", "NIEMANN-PICK DISEASE, TYPE D", "Type C1 Niemann-Pick Disease", "Niemann-Pick's Disease Type D", "Niemann-PICK disease, type C1", "Niemann Pick Disease, Type C1", "Niemann-Pick Disease, Type C1", "Niemann-Pick disease, type C1", "Niemann Pick's Disease Type D", "NIEMANN-PICK DISEASE, TYPE C1", "Niemann Pick Disease, Nova Scotian", "Niemann-Pick disease, Nova Scotian", "Niemann-Pick Disease, Nova Scotian", "Niemann-Pick disease, nova Scotian type", "Niemann-Pick disease, type D (disorder)", "NIEMANN-PICK DISEASE, NOVA SCOTIAN TYPE", "Niemann-Pick disease type D (diagnosis)", "Niemann-Pick Disease, Nova Scotian Type", "Niemann-Pick disease type C1 (diagnosis)", "Nova Scotia Niemann Pick Disease (Type D)", "Nova Scotia Niemann-Pick Disease (Type D)", "Niemann-Pick disease, subacute juvenile form", "Niemann Pick disease, Subacute Juvenile Form", "Niemann-Pick disease, Subacute Juvenile Form", "NIEMANN-PICK DISEASE, SUBACUTE JUVENILE FORM", "Niemann-Pick disease, chronic neuronopathic form", "Nova Scotia (Type D) Form of Niemann-Pick Disease", "Niemann-Pick disease without sphingomyelinase deficiency", "Niemann-Pick disease with cholesterol esterification block", "neurovisceral storage disease with vertical supranuclear ophthalmoplegia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Niemann-Pick disease, type C1", "shortest_name_length": 4}
{"curie": "UMLS:C1336296", "names": ["Stage II Liver Cancer", "Stage II Liver Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Liver Cancer", "shortest_name_length": 21}
{"curie": "UMLS:C2981390", "names": ["Stage IIIC Appendix Cancer", "Stage IIIC Appendix Carcinoma", "Stage IIIC Appendix Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Appendix Carcinoma AJCC v7", "shortest_name_length": 26}
{"curie": "MONDO:0010834", "names": ["HSCR5", "HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 5", "Hirschsprung disease, susceptibility to, 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hirschsprung disease, susceptibility to, 5", "shortest_name_length": 5}
{"curie": "UMLS:C4725047", "names": ["Soft Tissue Sarcoma, Excluding Rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Soft Tissue Sarcoma, Excluding Rhabdomyosarcoma", "shortest_name_length": 47}
{"curie": "UMLS:C0280366", "names": ["Relapsed Mouth Mucoepidermoid Carcinoma", "Recurrent Mouth Mucoepidermoid Carcinoma", "Relapsed Mucoepidermoid Carcinoma of Mouth", "Recurrent Mucoepidermoid Carcinoma of Mouth", "Relapsed Oral Cavity Mucoepidermoid Carcinoma", "Recurrent Oral Cavity Mucoepidermoid Carcinoma", "Relapsed Mucoepidermoid Carcinoma of the Mouth", "oral cavity mucoepidermoid carcinoma, recurrent", "Recurrent Mucoepidermoid Carcinoma of the Mouth", "Relapsed Mucoepidermoid Carcinoma of Oral Cavity", "Recurrent Mucoepidermoid Carcinoma of Oral Cavity", "Relapsed Mucoepidermoid Carcinoma of the Oral Cavity", "Recurrent Mucoepidermoid Carcinoma of the Oral Cavity", "recurrent mucoepidermoid carcinoma of the oral cavity", "Mucoepidermoid carcinoma of the oral cavity recurrent", "mucoepidermoid carcinoma of the oral cavity, recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mucoepidermoid carcinoma of the oral cavity recurrent", "shortest_name_length": 39}
{"curie": "UMLS:C3160764", "names": ["Metastases to pelvis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastases to pelvis", "shortest_name_length": 20}
{"curie": "MONDO:0033008", "names": ["GAMOS4", "Galloway-Mowat syndrome 4", "GALLOWAY-MOWAT SYNDROME 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Galloway-Mowat syndrome 4", "shortest_name_length": 6}
{"curie": "MONDO:0013934", "names": ["TIIAC", "MST1 deficiency", "STK4 deficiency", "STK4 DEFICIENCY", "MST1 DEFICIENCY", "CID due to STK4 deficiency", "combined immunodeficiency due to STK4 deficiency", "T-cell immunodeficiency, recurrent infections, autoimmunity, and cardiac malformations", "T-cell immunodeficiency, recurrent infections, and autoimmunity with or without CARDIAC malformations", "T-CELL IMMUNODEFICIENCY, RECURRENT INFECTIONS, AND AUTOIMMUNITY WITH OR WITHOUT CARDIAC MALFORMATIONS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined immunodeficiency due to STK4 deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0010979", "names": ["TS", "LQT8", "TIMOTHY syndrome", "Timothy Syndrome", "TIMOTHY SYNDROME", "Timothy syndrome", "LONG QT SYNDROME 8", "Long QT Syndrome 8", "long QT syndrome 8", "Long Qt Syndrome 8", "Long QT syndrome type 8", "long QT syndrome type 8", "Timothy syndrome (disorder)", "Timothy syndrome (diagnosis)", "long QT syndrome with syndactyly", "Long QT syndrome with syndactyly", "LONG QT SYNDROME WITH SYNDACTYLY", "long QT syndrome-syndactyly syndrome", "Long QT syndrome-syndactyly syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Timothy syndrome", "shortest_name_length": 2}
{"curie": "UMLS:C0855096", "names": ["Relapsed Small Lymphocytic Lymphoma", "relapsed small lymphocytic lymphoma", "Recurrent Small Lymphocytic Lymphoma", "recurrent small lymphocytic lymphoma", "small lymphocytic lymphoma, relapsed", "small lymphocytic lymphoma, recurrent", "Relapsed B-Cell Small Lymphocytic Lymphoma", "B-cell small lymphocytic lymphoma recurrent", "Recurrent B-Cell Small Lymphocytic Lymphoma", "Small lymphocyte B lymphoma (Lukes-Collins Classification) recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-cell small lymphocytic lymphoma recurrent", "shortest_name_length": 35}
{"curie": "MONDO:0005584", "names": ["congenital left-sided heart lesions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital left-sided heart lesions", "shortest_name_length": 35}
{"curie": "MONDO:0016912", "names": ["14q monosomy", "14q deletion", "monosomy 14q", "deletion 14q", "partial monosomy 14q", "chromosome 14q deletion", "partial deletion of chromosome 14q", "partial monosomy of chromosome 14q", "partial deletion of the long arm of chromosome 14", "partial monosomy of the long arm of chromosome 14", "partial deletion of the long arm of chromosome type 14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of the long arm of chromosome 14", "shortest_name_length": 12}
{"curie": "UMLS:C4288891", "names": ["Infant T-ALL", "T Acute Lymphoblastic Leukemia", "Infant T-Acute Lymphoblastic Leukemia", "Infant T Acute Lymphoblastic Leukemia", "Infant Precursor T Lymphoblastic Leukemia", "Infant Precursor T-Lymphoblastic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infant T Acute Lymphoblastic Leukemia", "shortest_name_length": 12}
{"curie": "UMLS:C0520546", "names": ["Pulmonary microemboli", "pulmonary microemboli", "Pulmonary microemboli (disorder)", "pulmonary microemboli (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pulmonary microemboli", "shortest_name_length": 21}
{"curie": "UMLS:C3897757", "names": ["Recurrent Central Nervous System Embryonal Neoplasm", "Recurrent Childhood Central Nervous System Embryonal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Central Nervous System Embryonal Neoplasm", "shortest_name_length": 51}
{"curie": "UMLS:C0236742", "names": ["PCP-related disorders", "Phencyclidine-Related Disorder", "Phencyclidine-related disorder", "Phencyclidine Related Disorders", "Phencyclidine-Related Disorders", "phencyclidine-related disorders", "Phencyclidine-related disorder, NOS", "Phencyclidine induced mental problem", "phencyclidine induced mental disorder", "PCP-induced organic mental disorder, NOS", "Phencyclidine-related disorder (disorder)", "Arylcyclohexylamine-related disorder, NOS", "Phencyclidine-induced mental disorder, NOS", "phencyclidine-related disorders (diagnosis)", "Organic mental disorder caused by phencyclidine", "phencyclidine induced mental disorder (diagnosis)", "Organic mental disorder caused by PCP (phencyclidine)", "Arylcyclohexylamine-induced organic mental disorder, NOS", "Organic mental disorder caused by phencyclidine (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Phencyclidine-Related Disorders", "shortest_name_length": 21}
{"curie": "MONDO:0016621", "names": ["JHD", "juvenile onset HD", "juvenile Huntington chorea", "Juvenile Huntington chorea", "Juvenile Huntington disease", "juvenile Huntington disease", "Juvenile Huntington Disease", "Huntington Disease, Juvenile", "Juvenile onset Huntington disease", "Juvenile-Onset Huntington Disease", "Juvenile Onset Huntington Disease", "Huntington disease juvenile onset", "Huntington disease, juvenile onset", "Huntington Disease, Juvenile Onset", "Huntington Disease, Juvenile-Onset", "Juvenile onset Huntington's disease", "Juvenile onset Huntington's disease (disorder)", "Juvenile onset Huntington's disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile Huntington disease", "shortest_name_length": 3}
{"curie": "UMLS:C0751008", "names": ["Ruptured Intracranial Arteriovenous Malformation", "Intracranial Arteriovenous Malformation, Ruptured"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intracranial Arteriovenous Malformation, Ruptured", "shortest_name_length": 48}
{"curie": "UMLS:C0018814", "names": ["Post Infarct Cardiac Rupture", "Post Infarction Heart Rupture", "Post-Infarction Heart Rupture", "Heart Rupture, Post-Infarction", "Post-Infarction Heart Ruptures", "Rupture, Post-Infarction Heart", "Heart Rupture, Post Infarction", "Ruptures, Post-Infarction Heart", "Heart Ruptures, Post-Infarction", "Post-Infarction Cardiac Rupture", "Cardiac Rupture, Post-Infarction", "Rupture, Post-Infarction Cardiac", "Post-Infarction Cardiac Ruptures", "Cardiac Rupture, Post Infarction", "Myocardial rupture (post infarct)", "MYOCARDIAL RUPTURE (POST INFARCT)", "Ruptures, Post-Infarction Cardiac", "Cardiac Ruptures, Post-Infarction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Heart Rupture, Post-Infarction", "shortest_name_length": 28}
{"curie": "UMLS:C4521791", "names": ["IIIB", "Stage IIIB Gastric (Stomach) Cancer", "Pathologic Stage IIIB Gastric Cancer AJCC v8", "Pathologic Stage IIIB Gastric Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IIIB Gastric Cancer AJCC v8", "shortest_name_length": 4}
{"curie": "MONDO:0009261", "names": ["GM1G2", "Derry syndrome", "Derry's disease", "GM1 gangliosidosis type 2", "GM1 Gangliosidosis type II", "Type II GM1-Gangliosidosis", "Gangliosidosis GM1, Type 2", "GM1 gangliosidosis, type 2", "GM1-gangliosidosis, type 2", "Type II GM1-Gangliosidoses", "Juvenile GM1 gangliosidosis", "juvenile GM1 gangliosidosis", "GM1-Gangliosidosis, Type II", "Juvenile Gangliosidosis GM1", "GM1-GANGLIOSIDOSIS, TYPE II", "GM1-gangliosidosis, type II", "GM1 gangliosidosis, type II", "GM1 Gangliosidosis, Type II", "GM1-Gangliosidoses, Type II", "gangliosidosis GM1, type II", "Gangliosidosis GM1, Juvenile", "late-infantile GM1 gangliosidosis", "late infantile systemic lipidosis", "gangliosidosis GM1, juvenile type", "Late-infantile GM1 gangliosidosis", "gangliosidosis generalized GM1 type 2", "GM1 Gangliosidosis type II (diagnosis)", "Juvenile GM1 gangliosidosis (disorder)", "Gangliosidosis, Generalized GM1 Type 2", "Gangliosidosis, Generalized GM1, Type 2", "GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 2", "gangliosidosis, generalized GM1, type 2", "GANGLIOSIDOSIS, GENERALIZED GM1, TYPE II", "Gangliosidosis, Generalized GM1, Type II", "gangliosidosis generalized GM1 juvenile type", "gangliosidosis, generalized GM1, juvenile type", "GANGLIOSIDOSIS, GENERALIZED GM1, JUVENILE TYPE", "Gangliosidosis, Generalized GM1, Juvenile Type", "Gangliosidosis, Generalized GM1, Late-Infantile Type", "GANGLIOSIDOSIS, GENERALIZED GM1, LATE-INFANTILE TYPE", "gangliosidosis, generalized GM1, late-infantile type", "gangliosidosis GM1, late onset without bony involvement", "generalized gangliosidosis, juvenile type generalized juvenile gangliosidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "GM1 gangliosidosis type 2", "shortest_name_length": 5}
{"curie": "MONDO:0013517", "names": ["beta-thalassemia", "thalassemia, beta", "beta-thalassemia HBB/LCRB", "thalassemia, hispanic gamma-delta-beta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "beta-thalassemia HBB/LCRB", "shortest_name_length": 16}
{"curie": "UMLS:C1257806", "names": ["Chromosome instability", "Chromosome Instability", "Instability, Chromosome", "Chromosomal Instability", "chromosomal instability", "Chromosomal instability", "Instability, Chromosomal", "Chromosome Instabilities", "Instabilities, Chromosome", "Chromosomal Instabilities", "Instabilities, Chromosomal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chromosomal Instability", "shortest_name_length": 22}
{"curie": "MONDO:0014615", "names": ["TTD2", "photosensitive trichothiodystrophy 2", "trichothiodystrophy 2, photosensitive", "Trichothiodystrophy 2, Photosensitive", "TRICHOTHIODYSTROPHY 2, PHOTOSENSITIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichothiodystrophy 2, photosensitive", "shortest_name_length": 4}
{"curie": "MONDO:0003784", "names": ["Stage 0 Nasal Cavity Cancer", "stage 0 nasal cavity cancer", "Nasal Cavity Carcinoma in situ", "nasal cavity in situ carcinoma", "Stage 0 Nasal Cavity Carcinoma", "nasal cavity carcinoma in situ", "stage 0 nasal cavity carcinoma", "stage 0 carcinoma of nasal cavity", "carcinoma in situ of nasal cavity", "Stage 0 Carcinoma of Nasal Cavity", "Carcinoma in situ of nasal cavity", "Carcinoma in situ of Nasal Cavity", "carcinoma in situ of nasal cavities", "Carcinoma in situ of nasal cavities", "Carcinoma in situ of the Nasal Cavity", "carcinoma in situ of the nasal cavity", "Stage 0 Carcinoma of the Nasal Cavity", "stage 0 carcinoma of the nasal cavity", "Carcinoma in situ of nasal cavity, NOS", "Stage 0 Nasal Cavity Carcinoma AJCC v7", "Stage 0 Nasal Cavity Carcinoma AJCC v6", "Stage 0 Nasal Cavity Carcinoma AJCC v8", "stage 0 nasal cavity carcinoma aJCC v7", "stage 0 nasal cavity carcinoma aJCC v8", "stage 0 nasal cavity carcinoma aJCC v6", "Carcinoma in situ of nasal cavity (disorder)", "carcinoma in situ of nasal cavity (diagnosis)", "Stage 0 Nasal Cavity Cancer AJCC v6, v7, and v8", "stage 0 nasal cavity cancer aJCC v6, v7, and v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasal cavity carcinoma in situ", "shortest_name_length": 27}
{"curie": "MONDO:0009740", "names": ["Nfdr syndrome", "NFDR SYNDROME", "NEUROFACIODIGITORENAL SYNDROME", "neurofaciodigitorenal syndrome", "Neurofaciodigitorenal syndrome", "Freire Maia Pinheiro Opitz syndrome", "Freire-Maia Pinheiro Opitz syndrome", "Freire Maia-Pinheiro-Opitz syndrome", "neurofaciodigitorenal (NFDR) syndrome", "NFDR (neurofaciodigitorenal) syndrome", "Neurofaciodigitorenal syndrome (disorder)", "neurofaciodigitorenal syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurofaciodigitorenal syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0001668", "names": ["Pink tooth of Mummery", "pink tooth of mummery", "internal resorption tooth", "pink spot lesion of tooth", "Pink spot lesion of tooth", "tooth internal resorption", "Internal tooth resorption", "internal granuloma of pulp", "Internal granuloma of pulp", "Internal resorption of tooth", "internal resorption of tooth", "internal pathologic resorption", "internal pathological resorption", "Pathological resorption, internal", "Internal resorption of crown of tooth", "internal resorption of crown of tooth", "Internal resorption of tooth (disorder)", "Pathological tooth resorption - internal", "pathological tooth resorption - internal", "internal pathological resorption of tooth", "Pathological resorption of tooth internal", "internal pathological resorption (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "internal pathological resorption of tooth", "shortest_name_length": 21}
{"curie": "UMLS:C0271420", "names": ["CERUMINOSIS", "ceruminosis", "Ceruminosis", "excess ear wax", "excessive ear wax", "Excessive ear wax", "Excessive;ear wax", "Excess wax in ear", "ears excessive wax"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ceruminosis", "shortest_name_length": 11}
{"curie": "UMLS:C1335514", "names": ["Prostatic Chloroma", "Prostate Myeloid Sarcoma", "Prostatic Myeloid Sarcoma", "Prostate Extramedullary Myeloid Tumor", "Prostatic Extramedullary Myeloid Tumor", "Extramedullary Myeloid Tumor of Prostate", "Prostate Extramedullary Myeloid Neoplasm", "Prostatic Extramedullary Myeloid Neoplasm", "Extramedullary Myeloid Neoplasm of Prostate", "Extramedullary Myeloid Tumor of the Prostate", "Extramedullary Myeloid Neoplasm of the Prostate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Myeloid Sarcoma", "shortest_name_length": 18}
{"curie": "UMLS:C5419898", "names": ["Digestive System Inflammatory Myofibroblastic Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Digestive System Inflammatory Myofibroblastic Tumor", "shortest_name_length": 51}
{"curie": "MONDO:0011925", "names": ["CMD1A", "MDC1A", "laminin alpha-2 deficiency", "LAMA2-related muscular dystrophy", "LAMA2 congenital muscular dystrophy", "Congenital muscular dystrophy type 1A", "congenital muscular dystrophy type 1A", "MCD1A - muscular congenital dystrophy type 1A", "CMD1A - congenital muscular dystrophy type 1A", "Merosin-negative congenital muscular dystrophy", "merosin-negative congenital muscular dystrophy", "Muscular dystrophy congenital, merosin negative", "Merosin deficient congenital muscular dystrophy", "Merosin-deficient congenital muscular dystrophy", "merosin-deficient congenital muscular dystrophy", "Muscular Dystrophy, Congenital Merosin-Deficient", "Congenital muscular dystrophy type 1A (disorder)", "muscular dystrophy, congenital merosin-deficient", "MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT", "muscular dystrophy, congenital, merosin-deficient", "congenital merosin-deficient muscular dystrophy 1A", "muscular dystrophy, congenital merosin-deficient, 1A", "MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A", "Muscular dystrophy, congenital, merosin-deficient 1A", "Muscular Dystrophy, Congenital Merosin-Deficient, 1A", "Merosin-Deficient Congenital Muscular Dystrophy Type 1A", "congenital merosin-deficient muscular dystrophy type 1A", "merosin-deficient congenital muscular dystrophy type 1A", "congenital muscular dystrophy caused by mutation in LAMA2", "muscular dystrophy, congenital merosin-deficient, type 1A", "Merosin deficient congenital muscular dystrophy (disorder)", "Laminin subunit alpha 2-related congenital muscular dystrophy", "Congenital muscular dystrophy due to laminin alpha2 deficiency", "congenital muscular dystrophy due to laminin alpha2 deficiency", "Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency", "muscular dystrophy, congenital, due to partial LAMA2 deficiency", "MUSCULAR DYSTROPHY, CONGENITAL, DUE TO PARTIAL LAMA2 DEFICIENCY", "muscular dystrophy, congenital, merosin deficient or partially deficient"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital merosin-deficient muscular dystrophy 1A", "shortest_name_length": 5}
{"curie": "MONDO:0030010", "names": ["HH25", "hypogonadotropic hypogonadism 25 with anosmia", "HYPOGONADOTROPIC HYPOGONADISM 25 WITH ANOSMIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadotropic hypogonadism 25 with anosmia", "shortest_name_length": 4}
{"curie": "MONDO:0004281", "names": ["Vulvar Porocarcinoma", "Vulvar Eccrine Porocarcinoma", "vulvar eccrine porocarcinoma", "mammalian vulva eccrine porocarcinoma", "eccrine porocarcinoma of mammalian vulva"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar eccrine porocarcinoma", "shortest_name_length": 20}
{"curie": "UMLS:C1333277", "names": ["Dermatofibrosarcoma Protuberans with Giant Cell Fibroblastoma-Like Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dermatofibrosarcoma Protuberans with Giant Cell Fibroblastoma-Like Differentiation", "shortest_name_length": 82}
{"curie": "UMLS:C4744858", "names": ["Advanced Carcinoid Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Carcinoid Tumor", "shortest_name_length": 24}
{"curie": "MONDO:0004133", "names": ["mixed acidophil-basophil adenoma", "Mixed acidophil-basophil adenoma", "Mixed Acidophil-Basophil Adenoma", "Mixed Eosinophil-Basophil Adenoma", "mixed eosinophil-basophil adenoma", "Pituitary Gland Mixed Acidophil-Basophil Adenoma", "pituitary gland mixed acidophil-basophil adenoma", "pituitary gland mixed eosinophil-basophil adenoma", "mixed acidophil-basophil adenoma (morphologic abnormality)", "Mixed acidophil-basophil adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pituitary gland mixed eosinophil-basophil adenoma", "shortest_name_length": 32}
{"curie": "MONDO:0043544", "names": ["HAI", "cross infection", "Cross Infection", "CROSS INFECTION", "Cross infection", "Cross infections", "Infection, Cross", "cross infections", "Cross Infections", "infection, Cross", "infections, Cross", "Infections, Cross", "Hospital Infection", "hospital infection", "crossing infections", "hospital infections", "Infection, Hospital", "Hospital Infections", "infection, hospital", "nosocomial infection", "infections, hospital", "Infections, Hospital", "Nosocomial Infection", "Nosocomial infection", "nosocomial infections", "Infection, Nosocomial", "Nosocomial Infections", "infection, nosocomial", "Nosocomial infections", "Infections, Nosocomial", "infections, nosocomial", "institutional infection", "Hospital-Onset Infection", "hospital-onset infection", "Cross infection (disorder)", "hospital-acquired infection", "hospital acquired infection", "Hospital acquired infection", "Hospital-Acquired Infection", "NOSOCOMIAL ACQUIRED INFECTION", "nosocomial infectious disease", "Nosocomial infectious disease", "Healthcare-associated Infection", "Healthcare-associated infection", "Healthcare Associated Infection", "Healthcare associated infection", "Healthcare-Associated Infection", "Health Care Associated Infection", "Healthcare associated infections", "infection, Healthcare associated", "health care associated infection", "Infection, Healthcare Associated", "associated infection, Healthcare", "Healthcare Associated Infections", "infections, Healthcare associated", "Health Care Associated Infections", "health care associated infections", "associated infections, Healthcare", "Infections, Healthcare Associated", "Nosocomial infectious disease, NOS", "Hospitalization-associated infection", "Hospitalisation-associated infection", "Healthcare associated infectious disease", "Healthcare associated infectious disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nosocomial infection", "shortest_name_length": 3}
{"curie": "UMLS:C0235575", "names": ["Hemolytic reaction", "reaction hemolytic", "HEMOLYTIC REACTION", "hemolytic reaction", "haemolytic reaction", "Haemolytic reaction", "HAEMOLYTIC REACTION", "hemolytic reactions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Haemolytic reaction", "shortest_name_length": 18}
{"curie": "MONDO:0019741", "names": ["familial cystic renal disease", "hereditary cystic kidney disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial cystic renal disease", "shortest_name_length": 29}
{"curie": "MONDO:0017522", "names": ["hyperphalangy, bilateral", "supernumerary phalanx, bilateral", "supernumerary phalanges, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperphalangy, bilateral", "shortest_name_length": 24}
{"curie": "MONDO:0000544", "names": ["Mucosal Melanoma", "mucosal melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucosal melanoma", "shortest_name_length": 16}
{"curie": "MONDO:0020099", "names": ["inherited sideroblastic anemia", "constitutional sideroblastic anemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited sideroblastic anemia", "shortest_name_length": 30}
{"curie": "MONDO:0004914", "names": ["MALS", "Dunbar syndrome", "Dunbar Syndrome", "Syndrome, Dunbar", "marable's syndrome", "Marable's syndrome", "celiac axis syndrome", "Celiac axis syndrome", "Coeliac axis syndrome", "celiac access syndrome", "Harjola-Marable syndrome", "Celiac artery compression", "Coeliac artery compression", "Median arcuate ligament syndrome", "median arcuate ligament syndrome", "Median Arcuate Ligament Syndrome", "Celiac axis compression syndrome", "MEDIAN ARCUATE LIGAMENT SYNDROME", "a.coeliaca; compression syndrome", "celiac axis compression syndrome", "Celiac Trunk Compression Syndrome", "Coeliac axis compression syndrome", "a.coeliaca; syndrome, compression", "axis coeliac compression syndrome", "Celiac Artery Compression Syndrome", "Celiac artery compression syndrome", "celiac artery compression syndrome", "Coeliac artery compression syndrome", "compression; celiac artery syndrome", "syndrome; celiac artery, compression", "syndrome; compression, celiac artery", "compression; celiac artery, syndrome", "compression; syndrome, celiac artery", "CACS - Celiac axis compression syndrome", "CACS - Coeliac axis compression syndrome", "median arcuate ligament syndromic disease", "artery; compression, celiac artery syndrome", "syndromic disease of median arcuate ligament", "Celiac artery compression syndrome (disorder)", "celiac artery compression syndrome (diagnosis)", "Celiac Artery Stenosis from Compression by Median Arcuate Ligament of Diaphragm", "celiac artery stenosis from compression by median arcuate ligament of diaphragm", "CELIAC ARTERY STENOSIS FROM COMPRESSION BY MEDIAN ARCUATE LIGAMENT OF DIAPHRAGM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "celiac artery stenosis from compression by median arcuate ligament of diaphragm", "shortest_name_length": 4}
{"curie": "MONDO:0003528", "names": ["Volkmann's syndrome", "Volkmann Contracture", "Ischemic Contracture", "Volkmann contracture", "Contracture, Ischemic", "Contracture, Volkmann", "Volkmann Contractures", "Ischemic Contractures", "volkmanns contracture", "Volkmanns contracture", "Contractures, Ischemic", "volkmann's contracture", "Contractures, Volkmann", "Volkmann's contracture", "contracture; volkmann's", "volkmann's; contracture", "Volkmann Ischemic Contracture", "Volkmanns Ischemic Contracture", "volkmann's ischemic contracture", "volkmann's contracture ischemic", "Volkmann's ischemic contracture", "Volkmann's Ischemic Contracture", "contractures ischemic volkmann's", "Contracture, Volkmann's Ischemic", "Ischemic Contracture, Volkmann's", "Volkmann's ischaemic contracture", "volkmann's; ischemic contracture", "Volkmann's contracture (disorder)", "Volkmann's contracture (diagnosis)", "Volkmann's contracture (physical finding)", "contracture; muscle, ischemic (volkmann's)", "muscle; contracture, ischemic (volkmann's)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Volkmann contracture", "shortest_name_length": 19}
{"curie": "MONDO:0006010", "names": ["Viral Hemorrhagic Septicemia", "Viral hemorrhagic septicemia", "viral hemorrhagic septicemia", "Hemorrhagic Septicemia, Viral", "Septicemia, Viral Hemorrhagic", "Viral Haemorrhagic Septicaemia", "Haemorrhagic Septicaemia, Viral", "Septicaemia, Viral Haemorrhagic", "salmonid viral hemorrhagic septicemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "salmonid viral hemorrhagic septicemia", "shortest_name_length": 28}
{"curie": "MONDO:0018362", "names": ["AFP", "PIFP", "atypical facial pain", "persistent idiopathic facial pain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "persistent idiopathic facial pain", "shortest_name_length": 3}
{"curie": "UMLS:C4763566", "names": ["Colorectal Adenocarcinoma Metastatic in the Liver"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Adenocarcinoma Metastatic in the Liver", "shortest_name_length": 49}
{"curie": "UMLS:C0042656", "names": ["Vidian neuralgia", "Vidian Neuralgia", "Vidian Neuralgias", "Neuralgia, Vidian", "Neuralgias, Vidian", "Vidian neuralgia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neuralgia, Vidian", "shortest_name_length": 16}
{"curie": "UMLS:C4054943", "names": ["FSGS Tip Lesion Variant", "Focal Segmental Glomerulosclerosis Tip Lesion Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Focal Segmental Glomerulosclerosis Tip Lesion Variant", "shortest_name_length": 23}
{"curie": "MONDO:0044870", "names": ["Acquired torsion dystonia", "acquired torsion dystonia", "Acquired torsion dystonia NOS", "Acquired torsion dystonia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired torsion dystonia", "shortest_name_length": 25}
{"curie": "MONDO:0043154", "names": ["fetal ovarian cyst", "Fetal ovarian cyst", "Neonatal ovarian cyst", "neonatal ovarian cyst"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal ovarian cyst", "shortest_name_length": 18}
{"curie": "UMLS:C3897761", "names": ["Recurrent Anaplastic Large Cell Lymphoma", "Recurrent Childhood Anaplastic Large Cell Lymphoma", "recurrent childhood anaplastic large cell lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Anaplastic Large Cell Lymphoma", "shortest_name_length": 40}
{"curie": "UMLS:C1337010", "names": ["Conventional Extraskeletal Myxoid Chondrosarcoma", "Well Differentiated Extraosseous Myxoid Chondrosarcoma", "Extraskeletal Well Differentiated Myxoid Chondrosarcoma", "Well Differentiated Extraskeletal Myxoid Chondrosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conventional Extraskeletal Myxoid Chondrosarcoma", "shortest_name_length": 48}
{"curie": "UMLS:C0392318", "names": ["infection salivary gland", "Infection;salivary gland", "Salivary Gland Infection", "salivary gland infection", "Salivary gland infection", "SALIVARY GLAND INFECTION", "salivary gland; infection", "glands infection salivary", "gland infections salivary", "glands infections salivary", "Salivary gland infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Salivary Gland Infection", "shortest_name_length": 24}
{"curie": "MONDO:0021388", "names": ["Chest wall tumor", "Chest Wall Tumor", "chest wall tumor", "chest tumor wall", "CHEST WALL TUMOR", "chest tumors wall", "Chest wall tumour", "tumor of chest wall", "chest wall neoplasm", "Chest Wall Neoplasm", "Tumor of Chest Wall", "neoplasm of chest wall", "Neoplasm of Chest Wall", "Neoplasm of chest wall", "tumor of the chest wall", "Tumor of the Chest Wall", "neoplasm of the chest wall", "Neoplasm of the Chest Wall", "chest wall neoplasm (disease)", "Neoplasm of chest wall (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplasm of chest wall", "shortest_name_length": 16}
{"curie": "MONDO:0009767", "names": ["Cross", "Cross syndrome", "CROSS SYNDROME", "cross syndrome", "Kramer Syndrome", "Kramer syndrome", "KRAMER SYNDROME", "crossed syndrome", "Cross syndrome (disorder)", "Cross syndrome (diagnosis)", "Cross-McKusick-Breen syndrome", "Hypopigmentation and microphthalmia", "Oculocerebral-hypopigmentation syndrome", "oculocerebral hypopigmentation syndrome", "congenital malformation syndromes Cross", "oculocerebral syndrome with hypopigmentation", "Oculocerebral syndrome with hypopigmentation", "OCULOCEREBRAL SYNDROME WITH HYPOPIGMENTATION", "hypopigmentation oculocerebral syndrome Cross type", "Oculocerebral hypopigmentation syndrome Cross type", "Oculocerebral hypopigmentation syndrome, Cross type", "oculocerebral hypopigmentation syndrome, Cross type", "Gingival fibromatosis, hypopigmentation, microphthalmia, oligophrenia and athetosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculocerebral hypopigmentation syndrome, Cross type", "shortest_name_length": 5}
{"curie": "MONDO:0009490", "names": ["PLS", "Pls", "PALS", "Papillon Lefevre Disease", "Papillon-Lefevre disease", "Papillon-Lefevre Disease", "Papillon-Lefvre syndrome", "papillon lefevre syndrome", "papillon-lefevre syndrome", "Papillon-Lefevre syndrome", "Papillon-LEFèvre syndrome", "Papillon Lefevre syndrome", "PAPILLON-Lefevre syndrome", "Papillon-Lefèvre syndrome", "Papillon-Lefevre Syndrome", "PAPILLON-LEFEVRE SYNDROME", "Papillon Lefevre Syndrome", "Papillon-Lefèvre syndrome (disorder)", "Papillon-Lefevre syndrome (diagnosis)", "Keratosis Palmoplantar Periodontopathy", "Periodontosis-Papillon-Lefebvre syndrome", "keratosis palmoplantar - periodontopathy", "Keratosis Palmoplantar Periodontopathies", "Palmoplantar Periodontopathies, Keratosis", "Juvenile periodontosis with hyperkeratosis", "palmoplantar keratoderma with periodontosis", "Keratosis Palmoplantaris with Periodontopathia", "KERATOSIS PALMOPLANTARIS WITH PERIODONTOPATHIA", "Keratoris palmoplantaris with periodontopathia", "keratosis palmoplantaris with periodontopathia", "keratosis palmoplantar-periodontopathy syndrome", "Keratosis palmoplantar-periodontopathy syndrome", "hyperkeratosis palmoplantaris with periodontosis", "palmar-plantar hyperkeratosis and concomitant periodontal destruction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Papillon-Lefevre disease", "shortest_name_length": 3}
{"curie": "MONDO:0018621", "names": ["lymphoplasmacytic lymphoma without IgM production", "lymphoplasmacytic lymphoma without Immunoglobulin M production"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphoplasmacytic lymphoma without IgM production", "shortest_name_length": 49}
{"curie": "MONDO:0003164", "names": ["cauda equina tumor", "Cauda Equina Tumor", "Tumor of Cauda Equina", "tumor of Cauda equina", "tumor of cauda equina", "Cauda Equina Neoplasm", "cauda equina neoplasm", "Cauda equina neoplasms", "Cauda Equina Neoplasms", "Neoplasm of cauda equina", "neoplasm of cauda equina", "Neoplasm of Cauda Equina", "Tumor of the Cauda Equina", "tumor of the Cauda equina", "tumor of the Cauda Equina", "neoplasm of the Cauda equina", "Neoplasm of the Cauda Equina", "cauda equina neoplasm (disease)", "Neoplasm of cauda equina (disorder)", "neoplasm of cauda equina (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cauda equina neoplasm", "shortest_name_length": 18}
{"curie": "UMLS:C5239052", "names": ["Lumbosacral Spine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lumbosacral Spine Neoplasm", "shortest_name_length": 26}
{"curie": "MONDO:0013469", "names": ["RP38", "RETINITIS PIGMENTOSA 38", "retinitis pigmentosa 38", "MERTK retinitis pigmentosa", "retinitis pigmentosa type 38", "Rod-cone dystrophy, childhood-onset", "ROD-CONE DYSTROPHY, CHILDHOOD-ONSET", "retinitis pigmentosa caused by mutation in MERTK"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 38", "shortest_name_length": 4}
{"curie": "MONDO:0011724", "names": ["G1D", "GLUT1DS1", "GLUT1 DS", "GLUT1-DS", "De Vivo disease", "De Vivo syndrome", "Glut1 deficiency", "Classic GLUT1-DS", "Glut1 Deficiency Syndrome", "GLUT1 deficiency syndrome", "glut-1 deficiency syndrome", "GLUT-1 deficiency syndrome", "GLUT1 DEFICIENCY SYNDROME 1", "GLUT1 Deficiency Syndrome 1", "GLUT1 deficiency syndrome 1", "GLUT1 deficiency syndrome type 1", "Classic GLUT1 deficiency syndrome", "glucose transporter protein syndrome", "glucose transporter Protein syndrome", "Glucose Transporter Protein Syndrome", "glucose transporter type 1 deficiency", "Encephalopathy Due To Glut1 Deficiency", "encephalopathy due to GLUT1 deficiency", "Encephalopathy due to GLUT1 deficiency", "glucose transporter type1 (glut-1) deficiency", "Glucose transport defect, blood-brain barrier", "GLUCOSE TRANSPORT DEFECT, BLOOD-BRAIN BARRIER", "Glucose transporter type1 (GLUT-1) deficiency", "glucose Transport defect, blood-brain barrier", "glucose transport defect, blood-brain barrier", "Glucose transporter protein type 1 deficiency", "Glucose transporter type 1 deficiency syndrome", "glucose transporter type 1 deficiency syndrome", "Glucose Transporter Type 1 Deficiency Syndrome", "GLUT1 deficiency syndrome 1, autosomal recessive", "GLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE", "GLUT1 deficiency syndrome 1, infantile onset, severe", "Classic glucose transporter type 1 deficiency syndrome", "Glucose transporter protein type 1 deficiency (diagnosis)", "carbohydrate transport and metabolism disorder glucose protein type 1 deficiency", "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephalopathy due to GLUT1 deficiency", "shortest_name_length": 3}
{"curie": "UMLS:C0334277", "names": ["Secondary adenocarcinoma", "secondary adenocarcinoma", "Metastatic adenocarcinoma", "Metastatic Adenocarcinoma", "Adenocarcinoma metastatic", "metastatic adenocarcinoma", "adenocarcinoma metastatic", "ADENOCARCINOMA METASTATIC", "Adenocarcinoma, metastatic", "Adenocarcinoma, metastatic NOS", "Adenocarcinoma, metastatic, NOS", "Metastatic adenocarcinoma (disorder)", "secondary adenocarcinoma (diagnosis)", "Adenocarcinoma, metastatic (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma, metastatic", "shortest_name_length": 24}
{"curie": "MONDO:0005994", "names": ["trichostrongyloidiasis", "Trichostrongyloidiases", "Trichostrongyloidiasis", "Trichostrongyloidea infectious disease", "Trichostrongyloidea disease or disorder", "Trichostrongyloidea caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichostrongyloidiasis", "shortest_name_length": 22}
{"curie": "MONDO:0005197", "names": ["THYMUS", "Thymoma", "thymus tumor", "Thymus tumor", "Thymic Tumor", "Thymic tumor", "Thymus Tumor", "thymic tumor", "Thymic Tumors", "thymus tumors", "tumour thymus", "Tumor, Thymic", "Thymus Tumors", "Tumor, Thymus", "Tumors, Thymic", "Thymus--Tumors", "Tumors, Thymus", "tumor of thymus", "Tumor of thymus", "thymus neoplasm", "Thymic Neoplasm", "Thymus neoplasm", "thymic neoplasm", "Tumor of Thymus", "Thymus Neoplasm", "tumor of Thymus", "Thymus Neoplasms", "Thymic Neoplasms", "Neoplasm, Thymus", "Neoplasm, Thymic", "Tumour of thymus", "Neoplasms, Thymic", "Neoplasms, Thymus", "Neoplasm of Thymus", "Neoplasm of thymus", "neoplasm of Thymus", "neoplasm of thymus", "tumor of the Thymus", "Tumor of the Thymus", "Neoplasm of the thymus", "Neoplasm of the Thymus", "neoplasm of the Thymus", "thymus neoplasm (disease)", "Neoplasm of thymus (disorder)", "neoplasm of thymus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thymus neoplasm", "shortest_name_length": 6}
{"curie": "MONDO:0031257", "names": ["high altitude pulmonary edema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "high altitude pulmonary edema", "shortest_name_length": 29}
{"curie": "MONDO:0045070", "names": ["Digestive System Melanoma", "digestive system melanoma", "Gastrointestinal Melanoma", "gastrointestinal melanoma", "Gastrointestinal melanoma", "Digestive System Mucosal Melanoma", "digestive system melanoma (disease)", "melanoma (disease) of digestive system", "Mucosal Melanoma of the Digestive System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "digestive system melanoma", "shortest_name_length": 25}
{"curie": "MONDO:0009123", "names": ["ORTHYP1", "DBH deficiency", "dopamine b-hydroxylase", "noradrenaline deficiency", "Noradrenaline deficiency", "NORADRENALINE DEFICIENCY", "Norepinephrine deficiency", "ORTHOSTATIC HYPOTENSION 1", "NOREPINEPHRINE DEFICIENCY", "norepinephrine deficiency", "dopamine beta hydroxylase deficiency", "dopamine beta-hydroxylase deficiency", "Dopamine beta-hydroxylase deficiency", "Congenital dopamine beta hydroxylase deficiency", "Dopamine beta-hydroxylase deficiency (disorder)", "congenital dopamine beta-hydroxylase deficiency", "orthostatic hypotension 1, due to DBH deficiency", "dopamine BETA-HYDROXYLASE deficiency, congenital", "Dopamine beta Hydroxylase Deficiency, Congenital", "DOPAMINE BETA-HYDROXYLASE DEFICIENCY, CONGENITAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dopamine beta-hydroxylase deficiency", "shortest_name_length": 7}
{"curie": "MONDO:0010831", "names": ["Sdam", "SDAM", "sirenomelia", "Absent sacrum", "sacrum; absent", "Sacral Agenesis", "sacral agenesis", "absence; sacrum", "SACRAL AGENESIS", "Sacral agenesis", "agenesis; sacrum", "sacrum; agenesis", "Caudal dysplasia", "absence of sacrum", "caudal regression", "Caudal Regression", "Agenesis of sacrum", "Rudd Klimek syndrome", "Hypoplasia of sacrum", "Rudd-Klimek syndrome", "Absence of the sacrum", "Sacrococcygeal agenesis", "Caudal dysplasia sequence", "caudal regression syndrome", "Caudal regression syndrome", "CAUDAL REGRESSION SYNDROME", "Familial caudal dysgenesis", "Caudal Dysgenesis Syndrome", "CAUDAL DYSGENESIS SYNDROME", "Sacral agenesis (disorder)", "caudal dysgenesis syndrome", "Caudal regression sequence", "familial caudal dysgenesis", "Caudal dysgenesis syndrome", "Caudal Regression Syndrome", "Congenital absence of sacrum", "absence of sacrum (diagnosis)", "caudal dysgenesis familial type", "Caudal dysgenesis familial type", "Caudal regression syndrome (disorder)", "Familial caudal dysgenesis (disorder)", "sacral defect with anterior meningocele", "congenital spinal anomaly sacral agenesis", "Sacral defect and anterior sacral meningocele", "congenital spinal anomaly sacral agenesis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial caudal dysgenesis", "shortest_name_length": 4}
{"curie": "UMLS:C4288625", "names": ["NK-Cell Lymphoma, Unclassifiable"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "NK-Cell Lymphoma, Unclassifiable", "shortest_name_length": 32}
{"curie": "MONDO:0011146", "names": ["PKS", "Tetrasomy 12p", "12p tetrasomy", "tetrasomy 12p", "Killian syndrome", "tetrasomy type 12p", "Hexasomy 12p, Mosaic", "mosaic tetrasomy 12p", "HEXASOMY 12p, MOSAIC", "Hexasomy 12P, Mosaic", "12p mosaic tetrasomy", "TETRASOMY 12p, MOSAIC", "Tetrasomy 12p, mosaic", "tetrasomy 12P, Mosaic", "Tetrasomy 12p syndrome", "Pallister mosaic syndrome", "pallister killian syndrome", "isochromosome 12p syndrome", "Isochromosome 12P syndrome", "pallister-killian syndrome", "Pallister-Killian Syndrome", "Pallister-Killian syndrome", "PALLISTER-KILLIAN SYNDROME", "ISOCHROMOSOME 12p SYNDROME", "Isochromosome 12p syndrome", "Pallister Killian syndrome", "Pallister mosaic aneuploidy", "Isochromosome 12p mosaicism", "Killian-Teschler-Nicola syndrome", "Teschler-Nicola-Killian Syndrome", "Teschler-Nicola Killian syndrome", "Killian Teschler-Nicola syndrome", "chromosome 12p tetrasomy syndrome", "Pallister-Killian Mosaic Syndrome", "Tetrasomy 12p syndrome (disorder)", "Pallister-Killian mosaic syndrome", "Teschler-Nicola and Killian syndrome", "Pallister-Killian syndrome (diagnosis)", "chromosome 12, Isochromosome 12p syndrome", "Pallister-Killian syndrome, Somatic mosaicism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tetrasomy 12p", "shortest_name_length": 3}
{"curie": "MONDO:0012382", "names": ["HHF4", "M/SCHAD", "had deficiency", "HADH deficiency", "SCHAD deficiency", "HADHSC deficiency", "M-SCHAD deficiency", "SCHAD deficiency, formerly", "hyperinsulinism due to SCHAD deficiency", "Hyperinsulinism due to SCHAD deficiency", "familial hyperinsulinemic hypoglycemia 4", "HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 4", "hyperinsulinemic hypoglycemia, familial, 4", "Hyperinsulinemic Hypoglycemia, Familial, 4", "3-hydroxyacyl-CoA dehydrogenase deficiency", "3-hydroxylacyl-CoA dehydrogenase deficiency", "HADH hyperinsulinemic hypoglycemia (disease)", "hyperinsulinemic hypoglycemia, familial, type 4", "3-alpha hydroxyacyl-CoA dehydrogenase deficiency", "3-hydroxyacyl-Coenzyme A dehydrogenase deficiency", "hyperinsulinemic hypoglycemia due to HADH deficiency", "hyperinsulinism due to glutamodehydrogenase deficiency", "Hyperinsulinism due to glutamodehydrogenase deficiency", "3-Alpha-hydroxyacyl-Coenzyme A dehydrogenase deficiency", "L-3-Alpha-hydroxyacyl-CoA dehydrogenase, short chain, deficiency", "medium and short chain 3-hydroxyacyl-CoA dehydrogenase deficiency", "hyperinsulinemic hypoglycemia (disease) caused by mutation in HADH", "Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency", "hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency", "Hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency", "hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme a dehydrogenase deficiency", "Hyperinsulinemic hypoglycemia due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency", "hyperinsulinemic hypoglycemia due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency", "Hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperinsulinemic hypoglycemia, familial, 4", "shortest_name_length": 4}
{"curie": "MONDO:0005124", "names": ["Hansen", "leprosy", "LEPROSY", "Leprosy", "Leprosy NOS", "leprosy nos", "Leprosy, NOS", "Hansen Disease", "hansen disease", "Hansen disease", "HANSEN DISEASE", "hansens disease", "hansen's disease", "Hansen's disease", "Hansen's Disease", "Leprosy (disorder)", "Leprous infections", "leprosy (diagnosis)", "Leprosy, unspecified", "Disease;Hansens (Leprosy)", "Hansens (leprosy) disease", "Leprosy [Hansen's disease]", "Mycobacterium leprae infection", "Mycobacterium leprae infection NOS", "Infection due to Mycobacterium leprae", "infection due to Mycobacterium leprae", "Mycobacterium leprae infectious disease", "Mycobacterium leprae disease or disorder", "Mycobacterium leprae caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leprosy", "shortest_name_length": 6}
{"curie": "UMLS:C5204269", "names": ["Renal Schwannoma", "Kidney Schwannoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kidney Schwannoma", "shortest_name_length": 16}
{"curie": "UMLS:C0155870", "names": ["INFLUENZA PNEUMONIA", "influenza pneumonia", "Influenza/Pneumonia", "pneumonia; influenza", "Pneumonia influenzal", "influenza; pneumonia", "influenzal pneumonia", "Influenzal pneumonia", "Pneumonia;influenzal", "PNEUMONIA AND INFLUENZA", "Influenza and pneumonia", "Pneumonia and influenza", "Influenza with pneumonia", "influenza with pneumonia", "Influenza with pneumonia NOS", "Influenza and pneumonia (J09-J18)", "Primary influenza virus pneumonia", "Influenza with pneumonia, any form", "Pneumonia and influenza (disorder)", "influenza with pneumonia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pneumonia and influenza", "shortest_name_length": 19}
{"curie": "MONDO:0030864", "names": ["RTSC3", "RITSCHER-SCHINZEL SYNDROME 3", "Ritscher-Schinzel syndrome 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ritscher-Schinzel syndrome 3", "shortest_name_length": 5}
{"curie": "MONDO:0032616", "names": ["MC1DN10", "nuclear type mitochondrial complex I deficiency 10", "mitochondrial complex 1 deficiency, nuclear type 10", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 10", "shortest_name_length": 7}
{"curie": "UMLS:C0541742", "names": ["Vancomycin poisoning", "Vancomycin poisoning (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vancomycin poisoning", "shortest_name_length": 20}
{"curie": "UMLS:C0677722", "names": ["Stage IV Aggressive Non-Hodgkin Lymphoma", "stage IV aggressive adult non-Hodgkin lymphoma", "Stage IV Aggressive Adult Non-Hodgkin Lymphoma", "aggressive, stage IV adult non-Hodgkin lymphoma", "Aggressive Stage IV Adult Non-Hodgkin's Lymphoma", "Stage IV Aggressive Adult Non-Hodgkin's Lymphoma", "aggressive stage IV adult non-Hodgkin's lymphoma", "Aggressive Adult Non-Hodgkin's Lymphoma Stage IV", "aggressive adult non-Hodgkin's lymphoma stage IV", "stage IV aggressive adult non-Hodgkin's lymphoma", "metastatic aggressive adult non-Hodgkin's lymphoma", "Ann Arbor Stage IV Aggressive Adult Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage IV Aggressive Adult Non-Hodgkin Lymphoma", "shortest_name_length": 40}
{"curie": "UMLS:C3273016", "names": ["HGDN", "High Grade Liver Dysplastic Nodule", "High Grade Hepatic Dysplastic Nodule"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Liver Dysplastic Nodule", "shortest_name_length": 4}
{"curie": "UMLS:C4525863", "names": ["Stage IIIA Rectal Neuroendocrine Tumor", "Stage IIIA Rectal Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Rectal Neuroendocrine Tumor AJCC v8", "shortest_name_length": 38}
{"curie": "MONDO:0002026", "names": ["muguet", "thrush", "Muguet", "Candidosis", "Moniliasis", "Moniliases", "candidosis", "moniliasis", "MONILIASIS", "Candidiases", "Candidiasis", "Monilia NOS", "candidiasis", "CANDIDIASIS", "Candida NOS", "candidiases", "Moniliasis NOS", "Moniliasis, NOS", "Candidiasis NOS", "Candidosis, NOS", "Candidiasis, NOS", "candida infection", "monilia infection", "Candida Infection", "Monilia infection", "Candida infection", "Candida infections", "candidal infection", "Monilial infection", "monilial infection", "monilia; infection", "infection; monilia", "candida infections", "MONILIASIS MONILIA", "candida; infection", "Candida Infections", "Infection, Candida", "infection; candidal", "Candidal infections", "candidal infections", "systemic candidiasis", "Candidiasis (disorder)", "Candidal infection NOS", "candidiasis (diagnosis)", "disseminated candidiasis", "Candidiasis, unspecified", "Disseminated candidiasis", "Infection by Candida species", "Candidiasis of unspecified site", "Candida <Debaryomycetaceae> infection", "infections, Candida <Debaryomycetaceae>"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "candidiasis", "shortest_name_length": 6}
{"curie": "UMLS:C4330484", "names": ["Indolent T-Lymphoblastic Proliferation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Indolent T-Lymphoblastic Proliferation", "shortest_name_length": 38}
{"curie": "MONDO:0007797", "names": ["HDR", "HDRS", "HDR syndrome", "HDR SYNDROME", "Barakat Syndrome", "Barakat syndrome", "BARAKAT SYNDROME", "Nephrosis, nerve deafness, and hypoparathyroidism", "nephrosis, nerve deafness, and hypoparathyroidism", "NEPHROSIS, NERVE DEAFNESS, AND HYPOPARATHYROIDISM", "hypoparathyroidism-deafness-renal disease syndrome", "Hypoparathyroidism, deafness, renal disease syndrome", "Hypoparathyroidism, Deafness, and Renal Anomalies Syndrome", "hypoparathyroidism, deafness, and renal anomalies syndrome", "HYPOPARATHYROIDISM, SENSORINEURAL DEAFNESS, AND RENAL DISEASE", "Hypoparathyroidism, Sensorineural Deafness, And Renal Disease", "hypoparathyroidism, sensorineural deafness, and renal disease", "hypoparathyroidism, sensorineural deafness, and renal dysplasia", "Hypoparathyroidism, deafness, renal disease syndrome (disorder)", "Hypoparathyroidism-sensorineural deafness-renal disease syndrome", "Hypoparathyroidism-sensorineural hearing loss-renal disease syndrome", "HYPOPARATHYROIDISM, SENSORINEURAL DEAFNESS, AND RENAL DYSPLASIA SYNDROME", "hypoparathyroidism, sensorineural deafness, and renal dysplasia syndrome", "HDR (hypoparathyroidism, sensorineural deafness, renal disease) syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypoparathyroidism-deafness-renal disease syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0015244", "names": ["arca", "autosomal recessive cerebellar ataxia", "cerebellar ataxia, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive cerebellar ataxia", "shortest_name_length": 4}
{"curie": "UMLS:C3203552", "names": ["Fetal exposure timing unspecified", "Foetal exposure timing unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fetal exposure timing unspecified", "shortest_name_length": 33}
{"curie": "MONDO:0008274", "names": ["PFD", "fibrous dysplasia of bone", "Polyostotic Fibrous Dysplasia", "Polyostotic fibrous dysplasia", "polyostotic fibrous dysplasia", "Fibrous Dysplasia, Polyostotic", "Polyostotic Fibrous Dysplasia of Bone", "polyostotic fibrous dysplasia of bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyostotic fibrous dysplasia", "shortest_name_length": 3}
{"curie": "UMLS:C4726609", "names": ["Resectable Pancreatic Ductal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Pancreatic Ductal Adenocarcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0010867", "names": ["PARC SYNDROME", "PARC syndrome", "poikiloderma, alopecia, retrognathism, and cleft palate", "POIKILODERMA, ALOPECIA, RETROGNATHISM, AND CLEFT PALATE", "Poikiloderma, Alopecia, Retrognathism, and Cleft palate", "Poikiloderma-alopecia-retrognathism-cleft palate syndrome", "poikiloderma-alopecia-retrognathism-cleft palate syndrome", "Poikiloderma, alopecia, retrognathism, cleft palate syndrome", "PARC (poikiloderma, alopecia, retrognathism, cleft palate) syndrome", "Poikiloderma, alopecia, retrognathism, cleft palate syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PARC syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0015831", "names": ["unicornuate uterus", "unilateral aplasia of the mullerian ducts", "unilateral aplasia of the Müllerian ducts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "unilateral aplasia of the mullerian ducts", "shortest_name_length": 18}
{"curie": "UMLS:C4744378", "names": ["Metastatic Malignant Neoplasm in the Sellar Region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Malignant Neoplasm in the Sellar Region", "shortest_name_length": 50}
{"curie": "UMLS:C5419161", "names": ["COVID-19 Asymptomatic Laboratory-Confirmed", "Asymptomatic COVID-19 Infection Laboratory-Confirmed", "Asymptomatic SARS-CoV-2 Infection Laboratory-Confirmed"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Asymptomatic COVID-19 Infection Laboratory-Confirmed", "shortest_name_length": 42}
{"curie": "MONDO:0001593", "names": ["rectal disease", "Rectal Disease", "disease rectum", "rectum disease", "RECTAL DISORDER", "Disorder rectal", "Rectal Diseases", "DISORDER RECTAL", "rectal diseases", "diseases rectum", "Rectal disorder", "diseases rectal", "rectal disorder", "Rectal Disorder", "disorders rectal", "rectum; disorder", "Rectal Disorders", "Rectum--Diseases", "disease of rectum", "Disease of rectum", "disorder of rectum", "Disorder of rectum", "Rectal disorder NOS", "Rectal disorder, NOS", "Disease of rectum, NOS", "rectum disease or disorder", "disease (or disorder); rectum", "Disorder of rectum (disorder)", "disease or disorder of rectum", "disorder of rectum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rectal disorder", "shortest_name_length": 14}
{"curie": "MONDO:0001364", "names": ["Regular astigmatism", "regular astigmatism", "Astigmatism, regular", "Regular astigmatism (disorder)", "regular astigmatism (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "regular astigmatism", "shortest_name_length": 19}
{"curie": "UMLS:C0279794", "names": ["Recurrent Lip and Oral Cavity Cancer", "recurrent lip and oral cavity cancer", "lip and oral cavity cancer, recurrent", "oral cavity and lip cancer, recurrent", "Recurrent Lip and Oral Cavity Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Lip and Oral Cavity Carcinoma", "shortest_name_length": 36}
{"curie": "MONDO:0032885", "names": ["SEMDIST", "spondyloepimetaphyseal dysplasia, Isidor-Toutain type", "SPONDYLOEPIMETAPHYSEAL DYSPLASIA, ISIDOR-TOUTAIN TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepimetaphyseal dysplasia, Isidor-Toutain type", "shortest_name_length": 7}
{"curie": "MONDO:0018930", "names": ["monosomy 21", "Monosomy 21", "monosomy 21q", "deletion 21q", "21q monosomy", "21q deletion", "21q- syndrome", "monosomy type 21", "del(21) syndrome", "partial monosomy 21q", "21 monosomy syndrome", "21 deletion syndrome", "partial 21q monosomy", "Partial 21q monosomy", "21q deletion syndrome", "Chromosome 21 monosomy", "chromosome 21q deletion", "chromosome 21 deletion syndrome", "chromosome G1 deletion syndrome", "chromosome 21 monosomy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "monosomy 21", "shortest_name_length": 11}
{"curie": "UMLS:C1519782", "names": ["Undifferentiated Endocervical Sarcoma", "Endocervical Undifferentiated Sarcoma", "Undifferentiated Sarcoma of the Endocervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endocervical Undifferentiated Sarcoma", "shortest_name_length": 37}
{"curie": "MONDO:0009029", "names": ["Cranial Nerves, Congenital Paresis Of", "CRANIAL NERVES, CONGENITAL PARESIS OF", "cranial nerves, congenital paresis of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cranial nerves, congenital paresis of", "shortest_name_length": 37}
{"curie": "MONDO:0044663", "names": ["aquagenic keratoderma", "aquagenic wrinkling of the hands", "aquagenic wrinkling of the palms", "aquagenic palmoplantar keratoderma", "aquagenic syringeal acrokeratoderma", "transient reactive papulotranslucent acrokeratoderma", "Transient reactive papulotranslucent acrokeratoderma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aquagenic palmoplantar keratoderma", "shortest_name_length": 21}
{"curie": "MONDO:0014387", "names": ["LKENP", "ovarioleukodystrophy", "progressive leukoencephalopathy with ovarian failure", "LEUKOENCEPHALOPATHY, PROGRESSIVE, WITH OVARIAN FAILURE", "leukoencephalopathy, progressive, with ovarian failure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukoencephalopathy, progressive, with ovarian failure", "shortest_name_length": 5}
{"curie": "MONDO:0014817", "names": ["NPHS12", "nephrotic syndrome type 12", "nephrotic syndrome, type 12", "NEPHROTIC SYNDROME, TYPE 12", "NUP93 familial nephrotic syndrome", "nephrotic syndrome, type 12; NPHS12", "familial nephrotic syndrome caused by mutation in NUP93"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrotic syndrome, type 12", "shortest_name_length": 6}
{"curie": "UMLS:C0272427", "names": ["Nose injury", "Nose Trauma", "injury nose", "nose trauma", "NOSE TRAUMA", "Nose Injury", "Injury;nose", "nose injury", "Nasal injury", "nasal injury", "injuries nose", "nasal; injury", "injury; nasal", "injury of nose", "of nose injury", "Injury of nose", "injuries nasal", "Injury of nose NOS", "Injury of nose (disorder)", "injury of nose (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of nose", "shortest_name_length": 11}
{"curie": "MONDO:0033672", "names": ["Duane anomaly-myopathy-scoliosis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Duane anomaly-myopathy-scoliosis syndrome", "shortest_name_length": 41}
{"curie": "MONDO:0014961", "names": ["SPGF16", "SUN5 azoospermia", "spermatogenic failure 16", "SPERMATOGENIC FAILURE 16", "spermatogenic failure type 16", "acephalic spermatozoa syndrome", "ACEPHALIC SPERMATOZOA SYNDROME", "Acephalic spermatozoa syndrome", "spermatogenic failure 16; SPGF16", "azoospermia caused by mutation in SUN5", "Male infertility due to acephalic spermatozoa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 16", "shortest_name_length": 6}
{"curie": "UMLS:C0858357", "names": ["Esophageal stenosis acquired", "Oesophageal stenosis acquired"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal stenosis acquired", "shortest_name_length": 28}
{"curie": "UMLS:C1336145", "names": ["Stage IB Squamous Cell Lung Cancer", "Stage IB Squamous Cell Lung Carcinoma", "Stage IB Squamous Cell Carcinoma of Lung", "Stage IB Squamous Cell Carcinoma of the Lung", "Stage IB Lung Squamous Cell Carcinoma AJCC v7", "Stage IB Squamous Cell Lung Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Lung Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 34}
{"curie": "UMLS:C0220635", "names": ["Neck Squamous Cell CUP", "Neck Squamous Cell Carcinoma of Unknown Primary", "Metastatic Squamous Neck Cancer with Occult Primary", "metastatic squamous neck cancer with occult primary", "Metastatic squamous neck cancer with occult primary", "neck cancer, metastatic squamous with occult primary", "Metastatic Epidermoid Neck Cancer with Occult Primary", "occult primary cancer metastatic squamous to the neck", "Metastatic Squamous Cell Neck Cancer with Occult Primary", "Squamous Cell Cancer Metastatic to Neck, with Occult Primary", "Epidermoid Cancer Metastatic to the Neck with Occult Primary", "Epidermoid Carcinoma Metastatic to the Neck with Occult Primary", "Squamous Cell Cancer Metastatic to the Neck with Occult Primary", "Squamous Cell Carcinoma Metastatic in the Neck with Occult Primary", "Squamous Cell Carcinoma Metastatic to the Neck with Occult Primary", "epidermoid carcinoma, metastatic squamous neck cancer with occult primary", "metastatic squamous neck cancer with occult primary squamous cell carcinoma", "squamous cell carcinoma of the neck, metastatic squamous with occult primary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neck Squamous Cell Carcinoma of Unknown Primary", "shortest_name_length": 22}
{"curie": "MONDO:0008395", "names": ["ruvalcaba syndrome", "Ruvalcaba syndrome", "Ruvalcaba Syndrome", "RUVALCABA SYNDROME", "Ruvalcaba syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ruvalcaba syndrome", "shortest_name_length": 18}
{"curie": "UMLS:C1332205", "names": ["Lymphocyte-Rich Classical Hodgkin Lymphoma", "Adult Lymphocyte-Rich Classic Hodgkin Lymphoma", "Adult Lymphocyte Rich Classical Hodgkin Lymphoma", "Adult Lymphocyte-Rich Classical Hodgkin Lymphoma", "Adult Lymphocyte Rich Classical Hodgkin's Disease", "Adult Lymphocyte Rich Classical Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Lymphocyte-Rich Classical Hodgkin Lymphoma", "shortest_name_length": 42}
{"curie": "MONDO:0016940", "names": ["3p trisomy", "Trisomy 3p", "trisomy 3p", "3p+ syndrome", "Duplication 3p", "3p duplication", "dup(3p) syndrome", "partial trisomy 3p", "chromosome 3p trisomy", "3p duplication syndrome", "duplication 3p syndrome", "Chromosome 3, trisomy 3p", "chromosome 3p duplication", "partial trisomy of chromosome 3p", "chromosome 3p duplication syndrome", "partial duplication of chromosome 3p", "partial trisomy of the short arm of chromosome 3", "partial duplication of the short arm of chromosome 3", "partial duplication of the short arm of chromosome type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of the short arm of chromosome 3", "shortest_name_length": 10}
{"curie": "UMLS:C1333500", "names": ["EGIST", "Extragastrointestinal Stromal Tumor", "Extragastrointestinal Gastrointestinal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extragastrointestinal Gastrointestinal Stromal Tumor", "shortest_name_length": 5}
{"curie": "MONDO:0016189", "names": ["qualitative or quantitative defects of filamin C", "qualitative or quantitative defects of filamin type C"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of filamin C", "shortest_name_length": 48}
{"curie": "UMLS:C5205696", "names": ["Sinonasal Adenocarcinoma, Non-Intestinal-Type", "Nasal Cavity and Paranasal Sinus Adenocarcinoma, Non-Intestinal-Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Adenocarcinoma, Non-Intestinal-Type", "shortest_name_length": 45}
{"curie": "MONDO:0007636", "names": ["FNM", "FND", "FND1", "FRONTORHINY", "frontorhiny", "Frontorhiny", "frontonasal dysplasia", "Frontonasal Dysplasia", "FRONTONASAL DYSPLASIA", "Frontorhiny (disorder)", "Frontonasal Dysplasia 1", "frontonasal dysplasia 1", "FRONTONASAL DYSPLASIA 1", "frontonasal malformation", "FRONTONASAL MALFORMATION", "MEDIAN FACIAL CLEFT SYNDROME", "median Facial cleft syndrome", "Frontonasal dysplasia type 1", "frontonasal dysplasia type 1", "isolated median cleft syndrome", "ALX3-related frontonasal dysplasia", "Isolated median cleft face syndrome", "isolated median cleft face syndrome", "ALX homeobox 3-related frontonasal dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontorhiny", "shortest_name_length": 3}
{"curie": "MONDO:0004521", "names": ["Epithelioid Sarcoma", "epithelioid sarcoma", "adult epithelioid sarcoma", "Adult Epithelioid Sarcoma", "epithelioid sarcoma, adult", "sarcoma, epithelioid, adult", "epithelioid sarcoma of adults"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult epithelioid sarcoma", "shortest_name_length": 19}
{"curie": "MONDO:0009248", "names": ["FRUCTOSE AND GALACTOSE INTOLERANCE", "Fructose and Galactose Intolerance", "fructose and galactose intolerance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fructose and galactose intolerance", "shortest_name_length": 34}
{"curie": "MONDO:0020464", "names": ["euryblepharon", "Euryblepharon", "Kabuki syndrome eyelids", "congenital euryblepharon", "Congenital euryblepharon", "Euryblepharon (disorder)", "euryblepharon (physical finding)", "congenital euryblepharon (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "euryblepharon", "shortest_name_length": 13}
{"curie": "UMLS:C3897742", "names": ["Recurrent Subependymal Giant Cell Astrocytoma", "recurrent childhood subependymal giant cell astrocytoma", "Recurrent Childhood Subependymal Giant Cell Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Subependymal Giant Cell Astrocytoma", "shortest_name_length": 45}
{"curie": "UMLS:C1335910", "names": ["Salivary Gland Sialadenoma Papilliferum", "sialadenoma papilliferum of salivary gland", "sialadenoma papilliferum of salivary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sialadenoma papilliferum of salivary gland", "shortest_name_length": 39}
{"curie": "MONDO:0035447", "names": ["liver adenomatosis", "Hepatic adenomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "liver adenomatosis", "shortest_name_length": 18}
{"curie": "MONDO:0016429", "names": ["Marburg acute multiple sclerosis", "Acute multiple sclerosis Marburg type", "Acute multiple sclerosis, Marburg type", "acute multiple sclerosis, Marburg type", "Acute multiple sclerosis Marburg variant", "acute multiple sclerosis, Marburg variant", "Acute multiple sclerosis, Marburg variant", "Marburg acute multiple sclerosis (disorder)", "Marburg acute multiple sclerosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Marburg acute multiple sclerosis", "shortest_name_length": 32}
{"curie": "MONDO:0013028", "names": ["AMP deaminase deficiency", "Deficiency of AMP aminase", "Deficiency of AMP deaminase", "Muscle AMP deaminase deficiency", "Myoadenylate deaminase deficiency", "myoadenylate deaminase deficiency", "Muscle adenylate deaminase deficiency", "Deficiency of adenylic acid deaminase", "Myoadenylate deaminase deficiency myopathy", "Adenosine monophosphate deaminase deficiency", "adenosine monophosphate deaminase deficiency", "myoadenylate deaminase deficiency (diagnosis)", "Deficiency of adenosine monophosphate deaminase", "deficiency of adenosine monophosphate deaminase", "Myoadenylate Deaminase Deficiency, Myopathy due to", "Muscle adenosine monophosphate deaminase deficiency", "Deficiency of adenosine monophosphate deaminase (disorder)", "deficiency of adenosine monophosphate deaminase (diagnosis)", "Muscle adenosine monophosphate deaminase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenosine monophosphate deaminase deficiency", "shortest_name_length": 24}
{"curie": "MONDO:0010093", "names": ["Syndesmodysplasic Dwarfism", "syndesmodysplasic dwarfism", "SYNDESMODYSPLASIC DWARFISM", "Familial syndesmodysplasic dwarfism", "Laplane Fontaine Lagardere syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndesmodysplasic dwarfism", "shortest_name_length": 26}
{"curie": "UMLS:C1336769", "names": ["Topoisomerase II Inhibitor-Related AML", "Topoisomerase II Inhibitor Related Acute Myeloid Leukemia", "Topoisomerase II Inhibitor-Related Acute Myeloid Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Topoisomerase II Inhibitor-Related Acute Myeloid Leukemia", "shortest_name_length": 38}
{"curie": "MONDO:0022960", "names": ["dermatocardioskeletal syndrome boronne type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermatocardioskeletal syndrome boronne type", "shortest_name_length": 43}
{"curie": "MONDO:0013836", "names": ["COQ10D6", "primary coenzyme Q10 deficiency 6", "coenzyme Q10 deficiency, primary, 6", "COENZYME Q10 DEFICIENCY, PRIMARY, 6", "coenzyme Q10 deficiency, primary, type 6", "familial steroid-resistant nephrotic syndrome with sensorineural deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial steroid-resistant nephrotic syndrome with sensorineural deafness", "shortest_name_length": 7}
{"curie": "MONDO:0000333", "names": ["early congenital syphilis", "Early congenital syphilis", "SYPHILIS, CONGENITAL, EARLY", "SYPHILIS, CONGENITAL, INFANTILE", "early congenital syphilis (diagnosis)", "Early congenital syphilis, unspecified", "Early congenital syphilis (less than 2 years)", "Early congenital syphilis, NOS (less than 2 years)", "Congenital syphilis NOS, less than two years after birth", "Congenital syphilis NOS less than two years after birth.", "Early congenital syphilis (less than 2 years) (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early congenital syphilis", "shortest_name_length": 25}
{"curie": "MONDO:0011756", "names": ["SLSN4", "Senior-Loken syndrome 4", "SENIOR-Loken syndrome 4", "SENIOR-LOKEN SYNDROME 4", "NPHP4 Senior-Loken syndrome", "Senior-Loken syndrome type 4", "Senior-Loken syndrome caused by mutation in NPHP4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Senior-Loken syndrome 4", "shortest_name_length": 5}
{"curie": "MONDO:0002935", "names": ["penile basal cell cancer", "Penile Basal Cell Cancer", "penis basal cell carcinoma", "Penile Basal Cell Carcinoma", "penile basal cell carcinoma", "basal cell carcinoma of penis", "penis skin basal cell carcinoma", "basal cell carcinoma of the penis", "Basal Cell Carcinoma of the Penis", "skin basal cell carcinoma of penis", "skin of penis skin basal cell carcinoma", "basal cell carcinoma of penis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "penis basal cell carcinoma", "shortest_name_length": 24}
{"curie": "MONDO:0031322", "names": ["triopia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "triopia", "shortest_name_length": 7}
{"curie": "MONDO:0015660", "names": ["Sporadic fetal brain disruption sequence", "sporadic fetal brain disruption sequence", "Sporadic foetal brain disruption sequence", "Sporadic fetal brain disruption sequence (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sporadic fetal brain disruption sequence", "shortest_name_length": 40}
{"curie": "MONDO:0015668", "names": ["hereditary dentin defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary dentin defect", "shortest_name_length": 24}
{"curie": "MONDO:0014858", "names": ["MRD43", "HIVEP2-related intellectual disability", "autosomal dominant mental retardation 43", "mental retardation, autosomal dominant 43", "autosomal dominant intellectual disability 43", "autosomal dominant intellectual disability-43", "mental retardation, autosomal dominant type 43", "intellectual disability, autosomal dominant 43", "intellectual disability, autosomal dominant type 43", "autosomal dominant intellectual developmental disorder 43", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 43", "autosomal dominant non-syndromic intellectual disability 43", "HIVEP2 autosomal dominant non-syndromic intellectual disability", "autosomal dominant non-syndromic intellectual disability caused by mutation in HIVEP2", "Human immunodeficiency virus type I enhancer binding protein 2 related intellectual disability", "HIVEP2 (human immunodeficiency virus type I enhancer binding protein 2) related intellectual disability", "Human immunodeficiency virus type I enhancer binding protein 2 related intellectual disability (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 43", "shortest_name_length": 5}
{"curie": "MONDO:0020525", "names": ["TNDM", "transient neonatal diabetes mellitus", "Transient neonatal diabetes mellitus", "Transient Neonatal Diabetes Mellitus", "diabetes mellitus, transient neonatal", "Transitory neonatal diabetes mellitus", "Diabetes mellitus, transient neonatal", "transient neonatal diabetes mellitus (disease)", "Transitory neonatal diabetes mellitus (disorder)", "diabetes mellitus, 6q24-related transient neonatal", "chromosome 6-associated transient diabetes mellitus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transient neonatal diabetes mellitus", "shortest_name_length": 4}
{"curie": "MONDO:0005466", "names": ["HYPERSOMNIA", "Hypersomnia", "hypersomnia", "Hypersomnias", "Sleep too much", "sleep too much", "much sleep too", "too much sleep", "Excessive sleep", "excessive sleep", "Sleep excessive", "increased sleep", "Hypersomnia NOS", "Sleeps too much", "Hypersomnia, NOS", "sleeping too much", "much sleeping too", "excessive sleeping", "INCREASED SLEEPING", "Sleeping Excessive", "Excessive sleeping", "Excessive sleepiness", "excessive sleepiness", "hypersomnia (disease)", "Hypersomnia (disorder)", "hypersomnia (diagnosis)", "Hypersomnolence Disorder", "Hypersomnolence disorder", "hypersomnolence disorder", "Hypersomnia, unspecified", "Hypersomnolence Disorders", "sleep disorder hypersomnia", "SLEEP DISORDER HYPERSOMNIA", "sleeping too much (symptom)", "Excessive Somnolence Disorder", "sleep disorder hypersomnolence", "Excessive Somnolence Disorders", "Somnolence Disorder, Excessive", "sleeping too much (hypersomnia)", "hypersomnia type; sleep disorder", "sleep disorder; hypersomnia type", "Hypersomnia (excessive sleeping)", "Disorder of excessive somnolence", "Disorders of Excessive Somnolence", "hypersomnolence disorder (diagnosis)", "DOES (Disorders of Excessive Somnolence)", "DOESs (Disorders of Excessive Somnolence)", "Disorder of excessive somnolence (disorder)", "Disorders of excessive somnolence [hypersomnias]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypersomnia", "shortest_name_length": 11}
{"curie": "UMLS:C4329639", "names": ["CNS Solitary Fibrous Tumor, Grade 2", "Central Nervous System Hemangiopericytoma", "Central Nervous System Solitary Fibrous Tumor, Grade 2", "CNS Solitary Fibrous Tumor/Hemangiopericytoma, Grade 2", "Solitary fibrous tumor/hemangiopericytoma Grade 2 (CNS)", "Central Nervous System Solitary Fibrous Tumor/Hemangiopericytoma, Grade 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Solitary Fibrous Tumor, Grade 2", "shortest_name_length": 35}
{"curie": "MONDO:0100495", "names": ["distal titinopathy", "autosomal recessive distal titinopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive distal titinopathy", "shortest_name_length": 18}
{"curie": "UMLS:C1377917", "names": ["stage I nasopharynx cancer", "nasopharynx cancer, stage I", "Stage I Nasopharynx Carcinoma", "stage I nasopharyngeal cancer", "nasopharyngeal cancer, stage I", "Stage I Nasopharyngeal Carcinoma", "Stage I Carcinoma of Nasopharynx", "Stage I Carcinoma of the Nasopharynx", "Stage I Nasopharyngeal Throat Cancer", "Stage I Nasopharyngeal Cancer AJCC v6", "Stage I Nasopharynx Carcinoma AJCC v6", "Nasopharyngeal Cancer, Stage I AJCC v6", "Stage I Carcinoma of Nasopharynx AJCC v6", "Stage I Nasopharyngeal Carcinoma AJCC v6", "Stage I Carcinoma of the Nasopharynx AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Nasopharyngeal Carcinoma", "shortest_name_length": 26}
{"curie": "UMLS:C4763842", "names": ["Metastatic Nested Urothelial Carcinoma", "Metastatic Nested Bladder Urothelial Carcinoma", "Metastatic Nested Urothelial Carcinoma of the Bladder", "Metastatic Infiltrating Bladder Urothelial Carcinoma, Nested Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Infiltrating Bladder Urothelial Carcinoma, Nested Variant", "shortest_name_length": 38}
{"curie": "UMLS:C1706836", "names": ["Appendix Tubulovillous Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Appendix Tubulovillous Adenoma", "shortest_name_length": 30}
{"curie": "UMLS:C5206878", "names": ["Unresectable Meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Meningioma", "shortest_name_length": 23}
{"curie": "MONDO:0014334", "names": ["IMD22", "LCK Deficiency", "immunodeficiency 22", "Immunodeficiency 22", "IMMUNODEFICIENCY 22", "immunodeficiency type 22", "SCID due to LCK deficiency", "LCK-Associated Immunodeficiency", "LCK Deficiency (T Lymphocyte-specific protein TK)", "severe combined immunodeficiency due to LCK deficiency", "SCID due to lymphocyte-specific protein tyrosine kinase deficiency", "severe combined immunodeficiency due to lymphocyte-specific protein tyrosine kinase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe combined immunodeficiency due to LCK deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0012208", "names": ["IWC", "CRIE", "MAUIE", "AARAU DISEASE", "Aarau Disease", "Aarau disease", "MAUIE SYNDROME", "ichthyosis variegata", "Ichthyosis variegata", "ichthyosis with confetti", "ICHTHYOSIS WITH CONFETTI", "Ichthyosis with confetti", "Erythrokeratoderma, Reticular", "ERYTHROKERATODERMA, RETICULAR", "erythrokeratoderma, reticular", "congenital reticular ichthyosiform erythroderma", "Congenital reticular ichthyosiform erythroderma", "erythroderma, ichthyosiform, congenital reticular", "ERYTHRODERMA, ICHTHYOSIFORM, CONGENITAL RETICULAR", "CRIE - Congenital reticular ichthyosiform erythroderma", "Congenital reticular ichthyosiform erythroderma (disorder)", "ICHTHYOSIS VARIEGATA MICROPINNAE, ALOPECIA UNIVERSALIS, CONGENITAL ICHTHYOSIS, AND ECTROPION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital reticular ichthyosiform erythroderma", "shortest_name_length": 3}
{"curie": "MONDO:0000990", "names": ["Acute nontransmural infarction", "acute nontransmural infarction", "Acute subendocardial infarction", "acute subendocardial infarction", "acute subendocardial myocardial infarction", "Acute subendocardial infarction (disorder)", "acute subendocardial infarction (diagnosis)", "subendocardial myocardial infarction, acute", "subendocardial infarction acute myocardial infarction", "Acute myocardial infarction, subendocardial infarction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute subendocardial myocardial infarction", "shortest_name_length": 30}
{"curie": "MONDO:0018148", "names": ["VPTR", "retinal vasoproliferative tumor", "vasoproliferative tumor of retina", "vasoproliferative tumor of the retina", "vasoproliferative tumor of ocular fundus", "vasoproliferative tumor of the ocular fundus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vasoproliferative tumor of retina", "shortest_name_length": 4}
{"curie": "MONDO:0012509", "names": ["PPNAD1", "CUSHING SYNDROME, ADRENAL, DUE TO PPNAD1", "Cushing Syndrome, Adrenal, Due To PPNAD1", "Cushing syndrome, adrenal, due to PPNAD1", "ADRENOCORTICAL NODULAR DYSPLASIA, PRIMARY", "Adrenocortical Nodular Dysplasia, Primary", "adrenocortical nodular dysplasia, primary", "PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1", "pigmented nodular adrenocortical disease, primary, 1", "Pigmented Nodular Adrenocortical Disease, Primary, 1", "PRKAR1A primary pigmented nodular adrenocortical disease", "Pigmented Micronodular Adrenocortical Disease, Primary, 1", "pigmented micronodular adrenocortical disease, primary, 1", "PIGMENTED MICRONODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1", "pigmented nodular adrenocortical disease, primary, type 1", "primary pigmented nodular adrenocortical disease caused by mutation in PRKAR1A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pigmented nodular adrenocortical disease, primary, 1", "shortest_name_length": 6}
{"curie": "MONDO:0054697", "names": ["IMD11B", "CARD11/CID", "immunodeficiency 11B", "immunodeficiency 11B with ATOPIC dermatitis", "immunodeficiency 11b with atopic dermatitis", "Immunodeficiency 11B with Atopic Dermatitis", "IMMUNODEFICIENCY 11B WITH ATOPIC DERMATITIS", "immunodeficiency 11B with atopic dermatitis", "Atopic Dermatitis, Elevated IgE, and Eosinophilia", "atopic dermatitis, elevated IgE, and eosinophilia", "ATOPIC DERMATITIS, ELEVATED IgE, AND EOSINOPHILIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 11b with atopic dermatitis", "shortest_name_length": 6}
{"curie": "MONDO:0017405", "names": ["Del(1)(p21.3)", "Del(1)p(21.3)", "Monosomy 1p21.3", "monosomy 1p21.3", "1p21.3 microdeletion syndrome", "1p21.3 microdeletion syndrome (disorder)", "1p21.3 microdeletion syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "1p21.3 microdeletion syndrome", "shortest_name_length": 13}
{"curie": "UMLS:C0015697", "names": ["Arterial Fatty Streak", "Streak, Arterial Fatty", "Fatty Streak, Arterial", "Arterial Fatty Streaks"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arterial Fatty Streak", "shortest_name_length": 21}
{"curie": "MONDO:0016840", "names": ["Dup(17p)", "dup(17p)", "17p trisomy", "trisomy 17p", "Trisomy 17p", "17p+ syndrome", "Duplication 17p", "17p duplication", "trisomy type 17p", "dup(17p) syndrome", "partial trisomy 17p", "Trisomy 17p (disorder)", "chromosome 17p trisomy", "trisomy 17p (diagnosis)", "17p duplication syndrome", "duplication 17p syndrome", "chromosome 17p duplication", "Chromosome 17, trisomy 17p", "chromosome 17p duplication syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trisomy 17p", "shortest_name_length": 8}
{"curie": "UMLS:C0558353", "names": ["tongue cancer", "Tongue cancer", "Tongue Cancer", "carcinoma tongue", "tongue carcinoma", "Tongue Carcinoma", "Carcinoma;tongue", "TONGUE CARCINOMA", "Cancer of Tongue", "Tongue carcinoma", "TONGUE, CARCINOMA", "carcinoma of tongue", "Carcinoma of Tongue", "Carcinoma of tongue", "Cancer of the Tongue", "Carcinoma of the Tongue", "carcinoma of the tongue", "TONGUE CANCER, CARCINOMA", "Tongue carcinoma (disorder)", "carcinoma of tongue (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tongue Carcinoma", "shortest_name_length": 13}
{"curie": "UMLS:C0855262", "names": ["Grandiose Type Delusional Disorder", "Delusional disorder, grandiose type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Delusional disorder, grandiose type", "shortest_name_length": 34}
{"curie": "MONDO:0018992", "names": ["REIDEL STRUMA", "reidel struma", "RIEDEL STRUMA", "Riedel disease", "Riedel; struma", "struma; Riedel", "Woody thyroiditis", "Riedel Thyroiditis", "THYROIDITIS, WOODY", "thyroiditis; woody", "riedel thyroiditis", "Riedel thyroiditis", "woody; thyroiditis", "Riedel; thyroiditis", "THYROIDITIS, RIEDEL", "riedels thyroiditis", "thyroiditis; Riedel", "Riedel's thyroiditis", "Invasive thyroiditis", "Ligneous thyroiditis", "riedel's thyroiditis", "ligneous; thyroiditis", "THYROIDITIS, LIGNEOUS", "thyroiditis; ligneous", "THYROIDITIS, INVASIVE", "Struma fibrosa thyroid", "THYROIDITIS CHRONIC RIEDELS", "Riedel Fibrosing Thyroiditis", "Invasive fibrous thyroiditis", "Riedel fibrosing thyroiditis", "invasive fibrous thyroiditis", "IgG4-related thyroid disease", "THYROIDITIS CHRONIC <RIEDELS>", "Riedel's fibrosing thyroiditis", "Riedel's Fibrosing Thyroiditis", "Riedel's thyroiditis (disorder)", "Riedel's thyroiditis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IgG4-related thyroid disease", "shortest_name_length": 13}
{"curie": "MONDO:0016227", "names": ["ea syndrome", "Episodic Ataxia", "episodic ataxia", "Episodic ataxia", "Isaacs syndrome", "Ataxia, episodic", "Paroxysmal ataxia", "episodic ataxia syndrome", "Hereditary episodic ataxia", "Episodic ataxia (disorder)", "hereditary episodic ataxia", "ataxia hereditary episodic", "Episodic ataxia (diagnosis)", "Intermittent cerebellar ataxia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary episodic ataxia", "shortest_name_length": 11}
{"curie": "MONDO:0016755", "names": ["NFIB", "neurofibroma", "Neurofibroma", "neurofibromas", "Neurofibromas", "Neurofibromata", "Neurofibroma NOS", "[M]Neurofibromas", "Neurofibroma, NOS", "NEUROFIBROMATOSIS", "Neurofibromatoses", "Neurofibromatosis", "neurofibromatosis", "neurofibromatoses", "Benign neurofibroma", "neurofibroma, benign", "NEUROFIBROMA, BENIGN", "Neurofibromatosis NOS", "Multiple Neurofibroma", "multiple neurofibromas", "NEUROFIBROMA, MULTIPLE", "Multiple Neurofibromas", "NF - Neurofibromatosis", "Neurofibroma, Multiple", "Neurofibromatosis, NOS", "Neurofibroma (disorder)", "Neurofibromas, Multiple", "Multiple neurofibromatosis", "Neurofibromatosis syndrome", "Neurofibroma (WHO Grade I)", "Clinical neurofibromatosis", "neurofibroma (WHO grade I)", "multiple neurofibromatosis", "Neurofibromatosis Syndrome", "Neurofibromatosis Syndromes", "Syndrome, Neurofibromatosis", "Syndromes, Neurofibromatosis", "neurofibromatosis (diagnosis)", "Neurofibromatosis, unspecified", "Neurofibromatosis syndrome (disorder)", "Recklinghausen's disease (except of Bone)", "Neurofibromatosis (morphologic abnormality)", "Von Recklinghausen's disease (except of Bone)", "von Recklinghausen's disease (except of Bone)", "Benign neurofibroma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurofibroma", "shortest_name_length": 4}
{"curie": "UMLS:C0018839", "names": ["HEAT EXHAUSTION", "Heat exhaustion", "Heat Exhaustion", "heat exhaustion", "exhaustion heat", "exhaustion; heat", "Exhaustion, Heat", "Heat Prostration", "Heat prostration", "HEAT PROSTRATION", "heat; exhaustion", "heat prostration", "Prostration, Heat", "heat; prostration", "Heat exhaustion, NOS", "Heat prostration NOS", "Heat prostration, NOS", "Heat exhaustion (disorder)", "heat exhaustion (diagnosis)", "Heat exhaustion, unspecified", "Effects of heat exhaustion, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Heat Exhaustion", "shortest_name_length": 15}
{"curie": "MONDO:0012393", "names": ["inherited GS deficiency", "congenital glutamine deficiency", "glutamine deficiency, congenital", "Glutamine deficiency, congenital", "GLUTAMINE DEFICIENCY, CONGENITAL", "inherited glutamine synthetase deficiency", "GLUTAMINE SYNTHASE DEFICIENCY, CONGENITAL SYSTEMIC", "glutamine synthase deficiency, congenital systemic", "Glutamine synthase deficiency, congenital systemic", "Glutamine synthetase deficiency, congenital systemic", "glutamine synthetase deficiency, congenital systemic", "congenital brain dysgenesis due to glutamine synthetase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital brain dysgenesis due to glutamine synthetase deficiency", "shortest_name_length": 23}
{"curie": "UMLS:C5419899", "names": ["Digestive System Soft Tissue Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Digestive System Soft Tissue Neoplasm", "shortest_name_length": 37}
{"curie": "UMLS:C4524517", "names": ["Cutaneous Squamous Cell Carcinoma of the Head and Neck", "cutaneous squamous cell carcinoma of the head and neck", "Cutaneous squamous cell carcinoma of the head and neck"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous Squamous Cell Carcinoma of the Head and Neck", "shortest_name_length": 54}
{"curie": "MONDO:0002362", "names": ["Serous Surface Papilloma", "Serous surface papilloma", "serous surface papilloma", "Serous surface papilloma, NOS", "Serous surface papilloma (morphologic abnormality)", "serous surface papilloma (morphologic abnormality)", "serous surface papilloma NOS (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "serous surface papilloma", "shortest_name_length": 24}
{"curie": "MONDO:0004206", "names": ["Pulmonary Vein Leiomyosarcoma", "pulmonary vein leiomyosarcoma", "leiomyosarcoma of pulmonary vein", "Leiomyosarcoma of Pulmonary Vein", "leiomyosarcoma of the pulmonary Vein", "Leiomyosarcoma of the Pulmonary Vein", "leiomyosarcoma of the pulmonary vein"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary vein leiomyosarcoma", "shortest_name_length": 29}
{"curie": "UMLS:C1334664", "names": ["Mediastinal Lymphangioma", "Mediastinal Cystic Hygroma", "Lymphangioma of Mediastinum", "Cystic Hygroma of Mediastinum", "Lymphangioma of the Mediastinum", "Cystic Hygroma of the Mediastinum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mediastinal Lymphangioma", "shortest_name_length": 24}
{"curie": "UMLS:C5418812", "names": ["Advanced Endometrial Endometrioid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Endometrial Endometrioid Adenocarcinoma", "shortest_name_length": 48}
{"curie": "MONDO:0014398", "names": ["COXPD21", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 21", "combined oxidative phosphorylation deficiency 21", "Combined oxidative phosphorylation defect type 21", "combined oxidative phosphorylation defect type 21", "TARS2 combined oxidative phosphorylation deficiency", "combined oxidative phosphorylation deficiency type 21", "COXPD21 - combined oxidative phosphorylation defect type 21", "Combined oxidative phosphorylation defect type 21 (disorder)", "combined oxidative phosphorylation defect type 21 (diagnosis)", "combined oxidative phosphorylation deficiency caused by mutation in TARS2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation defect type 21", "shortest_name_length": 7}
{"curie": "UMLS:C2982591", "names": ["Congenital Amegakaryocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Amegakaryocytosis", "shortest_name_length": 28}
{"curie": "UMLS:C0878552", "names": ["Coronary Artery Ectasia", "Coronary artery ectasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Coronary artery ectasia", "shortest_name_length": 23}
{"curie": "MONDO:0001473", "names": ["hyperfunction; medulla", "medulla; hyperfunction", "Medulloadrenal hyperfunction", "medulloadrenal hyperfunction", "Adrenal medulla hyperfunction", "Adrenomedullary hyperfunction", "Medulloadrenal hyperfunction (disorder)", "medulloadrenal hyperfunction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "medulloadrenal hyperfunction", "shortest_name_length": 22}
{"curie": "MONDO:0014008", "names": ["PHLU", "Phosphohydroxylysinuria", "phosphohydroxylysinuria", "PHOSPHOHYDROXYLYSINURIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phosphohydroxylysinuria", "shortest_name_length": 4}
{"curie": "UMLS:C4553414", "names": ["Stage IIB Fallopian Tube Cancer", "Stage IIB Fallopian Tube Cancer AJCC v8", "Stage IIB Fallopian Tube Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Fallopian Tube Cancer AJCC v8", "shortest_name_length": 31}
{"curie": "MONDO:0007472", "names": ["cuticular drusen", "Cuticular drusen", "Drusen, Cuticular", "drusen, cuticular", "DRUSEN, CUTICULAR", "Basal Laminar Drusen", "basal laminar drusen", "BASAL LAMINAR DRUSEN", "Basal laminar drusen", "DRUSEN OF BRUCH MEMBRANE", "Drusen of Bruch Membrane", "drusen of Bruch membrane", "drusen of bruch membrane", "Basal laminar drusen (finding)", "BASAL LAMINAR DRUSEN (disorder)", "early adult-onset grouped drusen", "Drusen, Early Adult-Onset, Grouped", "drusen, early adult-onset, grouped", "DRUSEN, EARLY ADULT-ONSET, GROUPED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "basal laminar drusen", "shortest_name_length": 16}
{"curie": "MONDO:0005235", "names": ["SMM", "smoldering myeloma", "Smoldering myeloma", "Smoldering Myeloma", "Smoldering Myelomas", "Myeloma, Smoldering", "Smouldering myeloma", "Asymptomatic Myeloma", "asymptomatic myeloma", "Asymptomatic myeloma", "Smoldering multiple myeloma", "smoldering multiple myeloma", "Smoldering Multiple Myeloma", "Multiple Myeloma, Smoldering", "Smouldering multiple myeloma", "Smoldering Multiple Myelomas", "Smoldering myeloma (disorder)", "Asymptomatic multiple myeloma", "Asymptomatic Multiple Myeloma", "Smoldering myeloma (diagnosis)", "Asymptomatic Multiple Myelomas", "Multiple Myeloma, Asymptomatic", "smoldering plasma cell myeloma", "Smoldering Plasma Cell Myeloma", "Multiple Myelomas, Asymptomatic", "asymptomatic plasma cell myeloma", "Asymptomatic Plasma Cell Myeloma", "Asymptomatic multiple myeloma (disorder)", "smoldering Multiple myeloma/plasma cell myeloma", "Smoldering Multiple Myeloma/Plasma Cell Myeloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "smoldering plasma cell myeloma", "shortest_name_length": 3}
{"curie": "UMLS:C4054340", "names": ["Non-Obstructed Megaureter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Obstructed Megaureter", "shortest_name_length": 25}
{"curie": "MONDO:0004834", "names": ["Ischemic Fasciitis", "Ischemic fasciitis", "ischemic fasciitis", "Ischaemic fasciitis", "Ischemic fasciitis (disorder)", "Atypical Decubital Fibroplasia", "atypical decubital fibroplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ischemic fasciitis", "shortest_name_length": 18}
{"curie": "MONDO:0001944", "names": ["mixed malaria", "Mixed malaria", "Mixed malaria (disorder)", "mixed malaria (diagnosis)", "malaria by more than one parasite", "Malaria by more than one parasite", "Malaria fever by more than one parasite", "malaria fever by more than one parasite"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed malaria", "shortest_name_length": 13}
{"curie": "MONDO:0044982", "names": ["drug allergy", "Drug pseudoallergy", "drug pseudoallergy", "Drug pseudoallergy (diagnosis)", "drug-related disorder pseudoallergy", "Pseudoallergy to drug or medicament", "Nonallergic hypersensitivity to drug or medicament", "Non-allergic hypersensitivity to drug or medicament", "Non-allergic hypersensitivity to drug or medicament (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "drug pseudoallergy", "shortest_name_length": 12}
{"curie": "MONDO:0016067", "names": ["Crandall syndrome", "Crandall's syndrome", "alopecia deafness hypogonadism", "Crandall's syndrome (disorder)", "Alopecia-deafness-hypogonadism syndrome", "alopecia-deafness-hypogonadism syndrome", "Alopecia-hearing loss-hypogonadism syndrome", "Alopecia-sensorineural deafness-hypogonadism syndrome", "alopecia-sensorineural deafness-hypogonadism syndrome", "Alopecia-sensorineural hearing loss-hypogonadism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Crandall syndrome", "shortest_name_length": 17}
{"curie": "UMLS:C4744756", "names": ["Thyroid Gland Hemangioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Hemangioma", "shortest_name_length": 24}
{"curie": "MONDO:0003096", "names": ["Deep Angioma", "deep angioma", "deep hemangioma", "Deep Hemangioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deep hemangioma", "shortest_name_length": 12}
{"curie": "MONDO:0008075", "names": ["NF3", "neurinoma", "Neurinomatosis", "neurinomatosis", "Schwannomatosis", "schwannomatosis", "neurilemmomatosis", "Neurilemmomatosis", "Neurofibromatosis type 3", "neurofibromatosis type 3", "Schwannomatosis (disorder)", "schwannomatosis (diagnosis)", "congenital cutaneous neurilemmomatosis", "neurilemmomatosis congenital cutaneous", "neurilemmomatosis, congenital cutaneous"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schwannomatosis", "shortest_name_length": 3}
{"curie": "UMLS:C0521626", "names": ["bladder fibrosis", "Bladder fibrosis", "BLADDER FIBROSIS", "bladder; fibrosis", "fibrosis; bladder", "Fibrosis of urinary bladder", "bladder fibrosis (diagnosis)", "Fibrosis of urinary bladder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fibrosis of urinary bladder", "shortest_name_length": 16}
{"curie": "MONDO:0016956", "names": ["Trisomy 5q", "5q trisomy", "trisomy 5q", "5q syndrome", "5q+ syndrome", "Duplication 5q", "5q duplication", "dup(5q) syndrome", "partial trisomy 5q", "5q duplication syndrome", "duplication 5q syndrome", "Chromosome 5, trisomy 5q", "chromosome 5q duplication", "chromosome 5q trisomy syndrome", "partial trisomy of chromosome 5q", "chromosome 5q duplication syndrome", "partial duplication of chromosome 5q", "partial trisomy of the long arm of chromosome 5", "partial duplication of the long arm of chromosome 5", "partial trisomy of the long arm of chromosome type 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial trisomy of the long arm of chromosome 5", "shortest_name_length": 10}
{"curie": "MONDO:0019485", "names": ["IHHS", "HHE syndrome", "H-H-E syndrome", "hemiplegia-hemiconvulsion-epilepsy syndrome", "hemiconvulsion-hemiplegia-epilepsy syndrome", "Hemiconvulsion-hemiplegia-epilepsy syndrome", "Hemiplegia-hemiconvulsion-epilepsy syndrome", "Idiopathic hemiconvulsion-hemiplegia syndrome", "idiopathic hemiconvulsion-hemiplegia syndrome", "Hemiplegia-hemiconvulsion-epilepsy syndrome (disorder)", "hemiplegia-hemiconvulsion-epilepsy syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic hemiconvulsion-hemiplegia syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C5206452", "names": ["Stage IIIC1 Cervical Cancer FIGO 2018", "Stage IIIC1 Cervical Carcinoma FIGO 2018"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC1 Cervical Cancer FIGO 2018", "shortest_name_length": 37}
{"curie": "MONDO:0015201", "names": ["Aughton-Hufnagle syndrome", "ankyloblepharon filiforme-imperforate anus syndrome", "ankyloblepharon filiforme adnatum-imperforate anus syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ankyloblepharon filiforme-imperforate anus syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0020722", "names": ["CAON", "nephrolith", "Nephrolith", "Renal stone", "Renal Stone", "nephroliths", "RENAL STONE", "renal stone", "Stone;renal", "kidney stone", "renal stones", "Kidney stone", "KIDNEY STONE", "Stone;kidney", "Renal stones", "Kidney Stone", "KIDNEY STONES", "Stone, Kidney", "Renal Calculi", "Kidney Stones", "Renal calculi", "Kidney stones", "renal calculi", "kidney stones", "Renal calculus", "Calculi, Renal", "Stones, Kidney", "RENAL CALCULUS", "Calculus renal", "Renal Calculus", "renal calculus", "kidney calculi", "Kidney Calculi", "Nephrolithiasis", "CALCULUS KIDNEY", "Calculus;kidney", "Calculi, Kidney", "KIDNEY CALCULUS", "Stone in kidney", "Calculus kidney", "Calculus, Renal", "Kidney calculus", "kidney calculus", "Kidney Calculus", "KIDNEY, CALCULUS", "Kidneys--Calculi", "calculus; kidney", "Calculus, Kidney", "Renal calculus NOS", "Calculus of kidney", "calculus of kidney", "Calculus renal NOS", "calculus; nephritic", "Oxalate urolithiasis", "Oxalate nephrolithiasis", "Renal calculus or stone", "Ca oxalate urolithiasis", "Kidney stone (disorder)", "Ca oxalate kidney stone", "Ca2+ oxalate urolithiasis", "Ca2+ oxalate kidney stone", "Ca oxalate nephrolithiasis", "Ca2+ oxalate nephrolithiasis", "Calcium oxalate urolithiasis", "Calcium Oxalate Urolithiasis", "urolithiasis, calcium oxalate", "Urolithiasis, Calcium Oxalate", "UROLITHIASIS, CALCIUM OXALATE", "Calcium oxalate kidney stones", "calcium oxalate nephrolithiasis", "Calcium oxalate nephrolithiasis", "Nephrolithiasis, calcium oxalate", "nephrolithiasis, calcium oxalate", "NEPHROLITHIASIS, CALCIUM OXALATE", "Nephrolithiasis, Calcium Oxalate", "Calcium oxalate urolithiasis (disorder)", "nephrolithiasis susceptibility caused by SLC26A1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrolithiasis susceptibility caused by SLC26A1", "shortest_name_length": 4}
{"curie": "MONDO:0006631", "names": ["osteoarthritis, toe"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteoarthritis, toe", "shortest_name_length": 19}
{"curie": "UMLS:C5420308", "names": ["Unresectable Pleural Sarcomatoid Mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Pleural Sarcomatoid Mesothelioma", "shortest_name_length": 45}
{"curie": "UMLS:C0432416", "names": ["Trisomy 21, translocation", "translocation; trisomy 21", "Trisomy 21 - translocation", "21; trisomy, translocation", "trisomy; 21, translocation", "Partial Trisomy 21 Down Syndrome", "Down Syndrome, Partial Trisomy 21", "Partial trisomy 21 in Down syndrome", "syndrome; trisomy, 21, translocation", "trisomy; syndrome, 21, translocation", "Partial trisomy 21 in Down's syndrome", "chromosome; 21, trisomy, translocation", "Partial trisomy 21 in Down's syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Down Syndrome, Partial Trisomy 21", "shortest_name_length": 25}
{"curie": "UMLS:C3272463", "names": ["Ampulla of Vater Undifferentiated Carcinoma with Osteoclast-Like Giant Cells"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ampulla of Vater Undifferentiated Carcinoma with Osteoclast-Like Giant Cells", "shortest_name_length": 76}
{"curie": "MONDO:0013317", "names": ["Torsade de pointes short coupled variant", "TORSADE DE POINTES, SHORT-COUPLED VARIANT", "torsade DE pointes, short-coupled variant", "Torsade de pointes with short coupling interval syndrome", "torsade-de-pointes syndrome with short coupling interval", "Torsade-de-pointes syndrome with short coupling interval", "Torsade de pointes with short coupling interval syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "torsade-de-pointes syndrome with short coupling interval", "shortest_name_length": 40}
{"curie": "MONDO:0009079", "names": ["DOORS", "drc syndrome", "DRC SYNDROME", "DOOR Syndrome", "DOOR syndrome", "DOOR SYNDROME", "door syndrome", "DOORS syndrome", "Eronen syndrome", "ERONEN SYNDROME", "Eronen Syndrome", "Feinmesser-Zelig syndrome", "digitorenocerebral syndrome", "Digitorenocerebral Syndrome", "Digitorenocerebral syndrome", "DIGITORENOCEREBRAL SYNDROME", "digitorenocerebral (DRC) syndrome", "recessive deafness-onychodystrophy syndrome", "Brachydactyly due to Absence of Distal Phalanges", "BRACHYDACTYLY DUE TO ABSENCE OF DISTAL PHALANGES", "brachydactyly due to absence of distal phalanges", "Deafness, congenital onychodystrophy, recessive form", "Autosomal recessive deafness-onychodystrophy syndrome", "Autosomal recessive deafness onychodystrophy syndrome", "autosomal recessive deafness-onychodystrophy syndrome", "Autosomal recessive hearing loss-onychodystrophy syndrome", "deafness-onycho-osteodystrophy-mental retardation syndrome", "Deafness, Onycho-Osteodystrophy, mental Retardation syndrome", "Deafness-onychoosteodystrophy-intellectual disability syndrome", "deafness-onychoosteodystrophy-intellectual disability syndrome", "Hearing loss-onychoosteodystrophy-intellectual disability syndrome", "DOOR (deafness-onychodystrophy-osteodystrophy-retardation) syndrome", "deafness onychodystrophy osteodystrophy and mental retardation syndrome", "deafness-onychodystrophy-osteodystrophy-intellectual disability syndrome", "Deafness-onychodystrophy-osteodystrophy-intellectual disability syndrome", "Deafness, Onychodystrophy, Osteodystrophy, And Mental Retardation Syndrome", "Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome", "deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome", "Hearing loss-onychodystrophy-osteodystrophy-intellectual disability syndrome", "deafness onychodystrophy osteodystrophy and intellectual disability syndrome", "Deafness-onychodystrophy-osteodystrophy-intellectual disability-seizures syndrome", "deafness-onychodystrophy-osteodystrophy-intellectual disability-seizures syndrome", "deafness, onychodystrophy, osteodystrophy, mental retardation, and seizures syndrome", "DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME", "Hearing loss-onychodystrophy-osteodystrophy-intellectual disability-seizures syndrome", "Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome (disorder)", "deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome (diagnosis)", "deafness, onychodystrophy, osteodystrophy, intellectual disability, and seizures syndrome", "DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, IMPAIRED INTELLECTUAL DEVELOPMENT, AND SEIZURES SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DOORS syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C4553580", "names": ["Stage III Urethral Cancer", "Stage III Urethral Cancer AJCC v8", "Stage III Urethral Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Urethral Cancer AJCC v8", "shortest_name_length": 25}
{"curie": "UMLS:C5206858", "names": ["Locally Advanced Oropharyngeal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Oropharyngeal Squamous Cell Carcinoma", "shortest_name_length": 54}
{"curie": "UMLS:C0268383", "names": ["Type VI Familial Amyloid Polyneuropathy", "Familial amyloid polyneuropathy, type VI", "Familial Amyloid Polyneuropathy, Type VI", "Familial amyloid polyneuropathy, 60 Ala-for-Thr", "Appalachian Type Familial Amyloid Polyneuropathy", "Familial amyloid polyneuropathy, Appalachian type", "Familial Amyloid Polyneuropathy, Appalachian Type", "Familial amyloid polyneuropathy, type VI (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Familial amyloid polyneuropathy, type VI", "shortest_name_length": 39}
{"curie": "UMLS:C1096388", "names": ["Arteriovenous fistula site complication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arteriovenous fistula site complication", "shortest_name_length": 39}
{"curie": "UMLS:C5447323", "names": ["Immunodeficiencies Affecting Cellular and Humoral Immunity/ Severe Combined Immune Deficiency", "Immunodeficiencies Affecting Cellular and Humoral Immunity - Severe Combined Immune Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immunodeficiencies Affecting Cellular and Humoral Immunity - Severe Combined Immune Deficiency", "shortest_name_length": 93}
{"curie": "MONDO:0007927", "names": ["Macroglossia", "Giant tongue", "macroglossia", "Enlarged tongue", "congenital macroglossia", "Congenital macroglossia", "macroglossia (diagnosis)", "tongue; hypertrophy, congenital", "hypertrophy; tongue, congenital", "Congenital hypertrophy of tongue", "Congenital macroglossia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital macroglossia", "shortest_name_length": 12}
{"curie": "UMLS:C4521716", "names": ["Stage II Esophageal Adenocarcinoma", "Postneoadjuvant Therapy Stage II Esophageal Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postneoadjuvant Therapy Stage II Esophageal Adenocarcinoma AJCC v8", "shortest_name_length": 34}
{"curie": "UMLS:C4682932", "names": ["Bladder Cancer by AJCC v8 Stage", "Bladder Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder Cancer by AJCC v8 Stage", "shortest_name_length": 31}
{"curie": "UMLS:C4763895", "names": ["H influenze type B Meningitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "H influenze type B Meningitis", "shortest_name_length": 29}
{"curie": "MONDO:0010486", "names": ["PPKMX", "OLMSX", "X-linked Olmsted syndrome", "Olmsted syndrome, X-linked", "OLMSTED SYNDROME, X-LINKED", "Olmsted syndrome, X-linked, X-linked recessive", "X-linked mutilating palmoplantar keratoderma with periorificial keratotic plaques", "PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTIC PLAQUES, X-LINKED", "palmoplantar keratoderma, mutilating, with periorificial keratotic plaques, X-linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Olmsted syndrome, X-linked", "shortest_name_length": 5}
{"curie": "MONDO:0007418", "names": ["DARWINIAN NOTCH", "Darwinian Notch", "DARWINIAN POINT OF PINNA", "Darwinian point of Pinna", "DARWINIAN TUBERCLE OF PINNA", "Darwinian tubercle of pinna"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Darwinian tubercle of pinna", "shortest_name_length": 15}
{"curie": "MONDO:0021238", "names": ["Cornea Tumor", "cornea tumor", "corneal tumor", "Corneal Tumor", "cornea neoplasm", "Tumor of cornea", "Cornea Neoplasm", "tumor of cornea", "Tumor of Cornea", "Tumour of cornea", "corneal neoplasm", "Corneal Neoplasm", "Corneal neoplasm", "Neoplasm of Cornea", "neoplasm of cornea", "Neoplasm of cornea", "eye neoplasm cornea", "Tumor of the Cornea", "tumor of the cornea", "Neoplasm of the Cornea", "neoplasm of the cornea", "cornea neoplasm (disease)", "Neoplasm of cornea (disorder)", "Neoplasm of cornea (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cornea neoplasm", "shortest_name_length": 12}
{"curie": "MONDO:0006686", "names": ["Brainstem Stroke", "stroke brainstem", "brainstem stroke", "Brain stem stroke", "Stroke, Brainstem", "brainstem strokes", "brainstem infarct", "Brainstem Infarct", "Brain stem infarct", "Brain Stem Infarct", "brain stem infarct", "Stem Infarct, Brain", "Brain Stem Infarcts", "Infarct, Brain Stem", "Stem Infarcts, Brain", "Brainstem infarction", "brainstem infarction", "Infarcts, Brain Stem", "Brainstem Infarction", "brain stem infarction", "Brainstem Infarctions", "Infarction, Brainstem", "BRAIN STEM INFARCTION", "Brain stem infarction", "Brain Stem Infarction", "Brain Stem Infarctions", "Infarction, Brain Stem", "Infarctions, Brainstem", "Infarctions, Brain Stem", "Infarction of brain stem", "brainstem brain infarction", "brain infarction of brainstem", "brainstem strokes (diagnosis)", "Brain stem infarction (disorder)", "brain stem infarction (diagnosis)", "cerebral infarction posterior circulation brain stem infarction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brain stem infarction", "shortest_name_length": 16}
{"curie": "UMLS:C0262517", "names": ["Stage IIB Hodgkin Lymphoma", "Stage IIB Hodgkin's Disease", "Hodgkin's Disease Stage IIB", "HODGKIN'S DISEASE STAGE IIB", "Stage IIB Hodgkin's Lymphoma", "Hodgkin's Lymphoma Stage IIB", "Ann Arbor Stage IIB Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage IIB Hodgkin Lymphoma", "shortest_name_length": 26}
{"curie": "MONDO:0013543", "names": ["TRYPSINOGEN DEFICIENCY", "Trypsinogen deficiency", "trypsinogen deficiency", "Pancreatic trypsinogen deficiency", "Congenital trypsinogen deficiency", "Trypsinogen deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trypsinogen deficiency", "shortest_name_length": 22}
{"curie": "MONDO:0014095", "names": ["CMD1JJ", "dilated cardiomyopathy 1JJ", "cardiomyopathy, dilated, 1JJ", "CARDIOMYOPATHY, DILATED, 1JJ", "dilated cardiomyopathy type 1JJ", "cardiomyopathy, dilated, type 1Jj", "LAMA4 familial isolated dilated cardiomyopathy", "familial isolated dilated cardiomyopathy caused by mutation in LAMA4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1JJ", "shortest_name_length": 6}
{"curie": "UMLS:C5421272", "names": ["EBV-Positive Inflammatory Follicular Dendritic Cell Sarcoma of the Digestive System", "Epstein-Barr Virus-Positive Inflammatory Follicular Dendritic Cell Sarcoma of the Digestive System", "Epstein-Barr Virus Positive Inflammatory Follicular Dendritic Cell Sarcoma of the Digestive System", "Inflammatory Pseudotumor-Like Follicular/Fibroblastic Dendritic Cell Sarcoma of the Digestive System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "EBV-Positive Inflammatory Follicular Dendritic Cell Sarcoma of the Digestive System", "shortest_name_length": 83}
{"curie": "MONDO:0014207", "names": ["ARMD14", "age related macular degeneration 14", "MACULAR DEGENERATION, AGE-RELATED, 14", "macular degeneration, age-related, 14", "age related macular degeneration type 14", "macular Degeneration, age-related, type 14", "macular Degeneration, age-related, reduced risk of", "MACULAR DEGENERATION, AGE-RELATED, REDUCED RISK OF", "macular degeneration, age-related, 14, reduced risk of, digenic dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "age related macular degeneration 14", "shortest_name_length": 6}
{"curie": "UMLS:C0162625", "names": ["Phasmidia Infection", "Infection, Phasmidia", "Phasmidia Infections", "Infections, Phasmidia", "Secernentea Infection", "Secernentea Infections", "Infection, Secernentea", "Infections, Secernentea"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secernentea Infections", "shortest_name_length": 19}
{"curie": "MONDO:0012922", "names": ["IHPS5", "Pyloric Stenosis, Infantile Hypertrophic, 5", "PYLORIC STENOSIS, INFANTILE HYPERTROPHIC, 5", "pyloric stenosis, infantile hypertrophic, 5", "infantile hypertrophic pyloric stenosis type 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyloric stenosis, infantile hypertrophic, 5", "shortest_name_length": 5}
{"curie": "MONDO:0014313", "names": ["IMD20", "CD16 deficiency", "IMMUNODEFICIENCY 20", "immunodeficiency 20", "immunodeficiency type 20", "autosomal recessive primary immunodeficiency with defective spontaneous NK cell cytotoxicity", "autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity", "shortest_name_length": 5}
{"curie": "UMLS:C3641711", "names": ["ENSAT Stage III Adrenal Cortex Cancer", "ENSAT Stage III Adrenal Cortex Carcinoma", "ENSAT Stage III Adrenal Cortical Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ENSAT Stage III Adrenal Cortical Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0009928", "names": ["PULAM", "Alveolar microlithiasis", "alveolar microlithiasis", "LUNG, ALVEOLAR MICROLITHIASIS", "Pulmonary alveolar microlithiasis", "alveolar microlithiasis pulmonary", "PULMONARY ALVEOLAR MICROLITHIASIS", "Pulmonary Alveolar Microlithiasis", "pulmonary alveolar microlithiasis", "microlithiasis; alveolar, pulmonary", "PAM - Pulmonary alveolar microlithiasis", "Pulmonary alveolar microlithiasis (disorder)", "pulmonary alveolar microlithiasis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary alveolar microlithiasis", "shortest_name_length": 5}
{"curie": "MONDO:0014561", "names": ["MGA7", "MGCA7", "MGCA7B", "MEGCANN", "CLPB 3-methylglutaconic aciduria", "3-methylglutaconic aciduria type 7", "3-methylglutaconic aciduria type 7b", "3-Methylglutaconic aciduria, type 7", "3-methylglutaconic aciduria type VII", "3-methylglutaconic aciduria, type VIIB", "3-METHYLGLUTACONIC ACIDURIA, TYPE VIIB", "3-@METHYLGLUTACONIC ACIDURIA, TYPE VIIB", "MGA7 - 3-methylglutaconic aciduria type 7", "3-methylglutaconic aciduria type 7 (disorder)", "3-methylglutaconic aciduria type 7 (diagnosis)", "organic acidemias 3-methylglutaconic aciduria type 7", "CLBP (ClpB homolog, mitochondrial AAA ATPase chaperonin) deficiency", "3-methylglutaconic aciduria-cataract-neurologic involvement-neutropenia syndrome", "3-methylglutaconic aciduria with cataracts, neurologic involvement and neutropenia", "3-methylglutaconic aciduria, cataract, neurologic involvement, neutropenia syndrome", "3-METHYLGLUTACONIC aciduria with cataracts, neurologic involvement, and neutropenia", "3-methylglutaconic aciduria, type VII, with cataracts, neurologic involvement and neutropenia", "3-METHYLGLUTACONIC ACIDURIA WITH CATARACTS, NEUROLOGIC INVOLVEMENT, AND NEUTROPENIA, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "3-methylglutaconic aciduria, type VIIB", "shortest_name_length": 4}
{"curie": "MONDO:0004639", "names": ["ENTEROCOLITIS NECROTIZING", "enterocolitis necrotizing", "necrotizing enterocolitis", "enterocolitis, necrotizing", "perinatal necrotizing enterocolitis", "perinatal necrotising enterocolitis", "Perinatal necrotising enterocolitis", "Pseudomembranous enterocolitis in newborn", "pseudomembranous enterocolitis in newborn", "necrotizing enterocolitis in fetus or newborn", "Necrotizing enterocolitis in fetus OR newborn"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "perinatal necrotizing enterocolitis", "shortest_name_length": 25}
{"curie": "UMLS:C4725809", "names": ["Recurrent Malignant Male Reproductive System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Malignant Male Reproductive System Neoplasm", "shortest_name_length": 53}
{"curie": "MONDO:0010675", "names": ["MUSCULAR DYSTROPHY, CARDIAC TYPE", "muscular dystrophy, cardiac type", "Muscular Dystrophy, Cardiac Type", "Muscular dystrophy - cardiac type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy, cardiac type", "shortest_name_length": 32}
{"curie": "UMLS:C5238242", "names": ["Refractory Gastric Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Gastric Adenocarcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0012574", "names": ["PTLS", "trisomy 17p11.2", "Trisomy 17p11 2", "Trisomy 17p11.2", "Duplication 17p11 2", "Potocki-Lupski Syndrome", "Potocki-Lupski syndrome", "Potocki Lupski syndrome", "POTOCKI-LUPSKI SYNDROME", "17p11.2 Duplication Syndrome", "17p11.2 Duplication syndrome", "Duplication 17p11.2 syndrome", "Chromosome 17, trisomy 17p11 2", "17p11.2 microduplication syndrome", "chromosome 17p11.2 duplication syndrome", "Chromosome 17p11.2 Duplication Syndrome", "Potocki-Lupski syndrome, Isolated cases", "chromosome 17P11.2 Duplication syndrome", "CHROMOSOME 17p11.2 DUPLICATION SYNDROME", "17p11.2 microduplication syndrome (disorder)", "Potocki-Lupski syndrome (dup(17)(p11.2p11.2))"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Potocki-Lupski syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C5420022", "names": ["Sinonasal Keratinizing Squamous Cell Carcinoma", "Nasal Cavity and Paranasal Sinus Keratinizing Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Keratinizing Squamous Cell Carcinoma", "shortest_name_length": 46}
{"curie": "UMLS:C4724832", "names": ["Locally Advanced Thymic Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Thymic Carcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C0861585", "names": ["Stage I Mouth Epidermoid Carcinoma", "Stage I Epidermoid Carcinoma of Mouth", "Stage I Mouth Squamous Cell Carcinoma", "Stage I Squamous Cell Carcinoma of Mouth", "Stage I Oral Cavity Squamous Cell Cancer", "Stage I Oral Cavity Epidermoid Carcinoma", "Stage I Epidermoid Carcinoma of the Mouth", "Stage I Oral Cavity Squamous Cell Carcinoma", "Stage I Epidermoid Carcinoma of Oral Cavity", "Stage I Squamous Cell Carcinoma of the Mouth", "Stage I Squamous Cell Carcinoma of Oral Cavity", "Stage I Epidermoid Carcinoma of the Oral Cavity", "Squamous cell carcinoma of the oral cavity stage I", "Stage I Squamous Cell Carcinoma of the Oral Cavity", "Stage I Oral Cavity Squamous Cell Carcinoma AJCC v6", "Stage I Oral Cavity Squamous Cell Carcinoma AJCC v7", "Stage I Oral Cavity Squamous Cell Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Squamous cell carcinoma of the oral cavity stage I", "shortest_name_length": 34}
{"curie": "UMLS:C4683623", "names": ["Stage B Chronic Lymphocytic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage B Chronic Lymphocytic Leukemia", "shortest_name_length": 36}
{"curie": "MONDO:0041186", "names": ["Rowell syndrome", "Rowell's syndrome", "Erythema multiforme-like lupus erythematosus", "Erythema multiforme-like lupus erythematosus (disorder)", "Lupus erythematosus and erythema multiforme-like syndrome", "lupus erythematosus and erythema multiforme-like syndrome", "Lupus erythematosus and erythema multiforme-like syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rowell syndrome", "shortest_name_length": 15}
{"curie": "UMLS:C5420464", "names": ["Benign Head and Neck Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Head and Neck Neoplasm", "shortest_name_length": 29}
{"curie": "MONDO:0032680", "names": ["GDDI", "GLOBAL DEVELOPMENTAL DELAY WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT", "global developmental delay with or without impaired intellectual development"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "global developmental delay with or without impaired intellectual development", "shortest_name_length": 4}
{"curie": "MONDO:0005704", "names": ["Ciliophora Infection", "Infection, Ciliophora", "Ciliophora Infections", "Infections, Ciliophora", "Ciliophora infectious disease", "Ciliophora disease or disorder", "Disease due to ciliate protozoa", "Disease caused by ciliate protozoa", "Ciliophora caused disease or disorder", "DISEASES DUE TO OTHER CILIATE PROTOZOA, NEC", "Disease caused by ciliate protozoa (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ciliophora infectious disease", "shortest_name_length": 20}
{"curie": "MONDO:0008218", "names": ["HHD", "BCPM", "hailey disease", "hailey-Hailey disease", "hailey-hailey disease", "Hailey Hailey Disease", "Hailey-Hailey disease", "HAILEY-HAILEY DISEASE", "hailey hailey disease", "Hailey Hailey disease", "Hailey-Hailey Disease", "diseases hailey hailey", "benign chronic pemphigus", "Benign Chronic Pemphigus", "BENIGN CHRONIC PEMPHIGUS", "Familial benign pemphigus", "benign familial pemphigus", "Benign familial pemphigus", "Familial Benign Pemphigus", "familial benign pemphigus", "Benign Familial Pemphigus", "pemphigus; benign familial", "Familial Pemphigus, Benign", "pemphigus, benign familial", "PEMPHIGUS, BENIGN FAMILIAL", "Pemphigus, Benign Familial", "benign; familial pemphigus", "Familial Benign Chronic Pemphigus", "Chronic Benign Familial Pemphigus", "familial benign chronic pemphigus", "Benign familial chronic pemphigus", "Familial benign chronic pemphigus", "Familial benign pemphigus (disorder)", "Benign familial pemphigus [Hailey-Hailey]", "familial benign chronic pemphigus (diagnosis)", "Benign chronic familial pemphigus of Hailey-Hailey", "benign chronic familial pemphigus of Hailey-Hailey"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hailey-Hailey disease", "shortest_name_length": 3}
{"curie": "MONDO:0012575", "names": ["BOR2", "branchiootorenal syndrome 2", "Branchiootorenal Syndrome 2", "BRANCHIOOTORENAL SYNDROME 2", "branchiootorenal syndrome type 2", "SIX5 branchio-oto-renal syndrome", "branchio-oto-renal syndrome caused by mutation in SIX5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "branchiootorenal syndrome 2", "shortest_name_length": 4}
{"curie": "UMLS:C1879691", "names": ["Amegakaryocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Amegakaryocytosis", "shortest_name_length": 17}
{"curie": "MONDO:0003741", "names": ["juvenile granulosa cell tumor", "Juvenile Granulosa Cell Tumor", "Juvenile granulosa cell tumor", "juvenile; granulosa cell tumor", "Juvenile granulosa cell tumour", "juvenile granulosa cell tumour", "Granulosa cell tumor, juvenile", "tumor; granulosa cell, juvenile", "granulosa cell; tumor, juvenile", "[M] Juvenile granulosa cell tumor", "[M] Juvenile granulosa cell tumour", "Juvenile Type Granulosa Cell Tumor", "Juvenile type Granulosa cell tumor", "juvenile type granulosa cell tumor", "Juvenile type Granulosa cell tumour", "Juvenile Type Granulosa Cell Neoplasm", "juvenile type granulosa cell neoplasm", "Juvenile Testicular Granulosa Cell Tumor", "juvenile type testicular granulosa cell tumor", "Juvenile Type Testicular Granulosa Cell Tumor", "Juvenile type testicular granulosa cell tumor", "juvenile type testicular granulosa cell tumour", "juvenile granulosa cell tumor (morphologic abnormality)", "Juvenile granulosa cell tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile type testicular granulosa cell tumor", "shortest_name_length": 29}
{"curie": "UMLS:C5206799", "names": ["Cancer-related Cognitive Dysfunction", "Cancer-related Cognitive Difficulties"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cancer-related Cognitive Dysfunction", "shortest_name_length": 36}
{"curie": "UMLS:C0282313", "names": ["preneoplastic state", "Preneoplastic Condition", "Condition, Preneoplastic", "Preneoplastic Conditions", "Conditions, Preneoplastic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Condition, Preneoplastic", "shortest_name_length": 19}
{"curie": "UMLS:C4763392", "names": ["Refractory PVRL", "Refractory Primary Vitreoretinal Lymphoma", "Refractory Primary Vitreoretinal Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Primary Vitreoretinal Non-Hodgkin Lymphoma", "shortest_name_length": 15}
{"curie": "MONDO:0008373", "names": ["RATOR", "Retinal artery tortuousity", "Tortuous retinal arterioles", "Retinal arterial tortuosity", "retinal arterial tortuosity", "Retinal arteriolar tortuosity", "retinal arteriolar tortuosity", "tortuosity of retinal arteries", "Tortuosity of retinal arteries", "RETINAL ARTERIES, TORTUOSITY OF", "retinal arteries, tortuosity OF", "Retinal arterial tortuosity (finding)", "retinal arterial tortuosity (disease)", "retinal hemorrhage with vascular tortuosity", "Retinal hemorrhage with vascular tortuosity", "RETINAL HEMORRHAGE WITH VASCULAR TORTUOSITY", "Retinal haemorrhage with vascular tortuosity", "Familial isolated retinal arterial tortuosity", "Familial isolated retinal arterial tortuosity (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal arterial tortuosity", "shortest_name_length": 5}
{"curie": "MONDO:0006604", "names": ["Blush", "blush", "Rosacea", "ROSACEA", "rosacea", "flushes", "Blushes", "Rosaceas", "blushing", "Red face", "Blushing", "Blushings", "Ruddy face", "acne roscea", "Acne roscea", "acne rosacea", "Acne rosacea", "ACNE ROSACEA", "Acne Rosacea", "rosacea acne", "Acne;rosacea", "Acne, rosacea", "acne; rosacea", "Face goes red", "rosacea; acne", "Blushed cheeks", "FACIAL ERYTHEMA", "Red in the face", "Erythema facial", "Facial erythema", "disorders rosacea", "Acne erythematosa", "acne, erythematosa", "Blushing, function", "Rosacea (disorder)", "Acne, erythematosa", "rosacea (diagnosis)", "Rosacea, unspecified", "Blushing, function (observable entity)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rosacea", "shortest_name_length": 5}
{"curie": "MONDO:0032694", "names": ["MCPH25", "microcephaly 25, primary, autosomal recessive", "MICROCEPHALY 25, PRIMARY, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly 25, primary, autosomal recessive", "shortest_name_length": 6}
{"curie": "UMLS:C1740802", "names": ["Post procedural sepsis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post procedural sepsis", "shortest_name_length": 22}
{"curie": "UMLS:C1820377", "names": ["Type II reaction", "Type II Hypersensitivity", "type II hypersensitivity", "Type 2 hypersensitivity reaction", "Type 2 Hypersensitivity Reaction", "Gell and Coombs reaction type II", "Type II Hypersensitivity Reaction", "Hypersensitivity reaction type II", "type II cellular hypersensitivity", "Type II reaction (Gell and Coombs)", "Hypersensitivity reaction mediated by antibody", "Hypersensitivity reaction mediated by antibody (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type II cellular hypersensitivity", "shortest_name_length": 16}
{"curie": "MONDO:0012997", "names": ["HDKR", "HARDIKAR SYNDROME", "HARDIKAR syndrome", "Hardikar syndrome", "Cholestasis-pigmentary retinopathy-cleft palate syndrome", "cholestasis-pigmentary retinopathy-cleft palate syndrome", "Cholestasis with pigmentary retinopathy and cleft palate syndrome", "Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholestasis-pigmentary retinopathy-cleft palate syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0016358", "names": ["acrosclerosis", "sclerodactyly", "Sclerodactyly", "Acrosclerosis", "Acroscleroderma", "Limited scleroderma", "limited scleroderma", "SCLERODERMA LIMITED", "Limited Scleroderma", "Scleroderma, Limited", "Sclerodactyly (disorder)", "sclerodactyly (diagnosis)", "Limited systemic sclerosis", "limited systemic sclerosis", "systemic sclerosis, limited", "Systemic sclerosis, limited", "Limited Systemic Scleroderma", "Scleroderma, Limited Systemic", "Systemic Scleroderma, Limited", "Limited Systemic Sclerodermas", "Systemic Sclerodermas, Limited", "Sclerodermas, Limited Systemic", "sclerodactyly (physical finding)", "Systemic sclerosis sine scleroderma", "Limited cutaneous systemic sclerosis", "limited cutaneous systemic sclerosis", "Limited systemic sclerosis (disorder)", "limited cutaneous systemic scleroderma", "limited systemic sclerosis (diagnosis)", "Limited cutaneous systemic scleroderma", "Systemic sclerosis with limited cutaneous involvement", "Systemic sclerosis with limited cutaneous involvement (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "limited cutaneous systemic sclerosis", "shortest_name_length": 13}
{"curie": "UMLS:C2987173", "names": ["Pancreatic Solid Serous Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Solid Serous Adenoma", "shortest_name_length": 31}
{"curie": "MONDO:0001326", "names": ["Dead pulp", "Pulp Gangrene", "Pulp Necrosis", "Pulp gangrene", "necrotic pulp", "pulp necrosis", "Necrotic pulp", "Pulp necrosis", "Pulp Necroses", "Necroses, Pulp", "Necrosis, Pulp", "Pulp Gangrenes", "Gangrene, Pulp", "Dental necrosis", "Pulpal gangrene", "Gangrenes, Pulp", "Pulpal necrosis", "Devitalized pulp", "pulpal; gangrene", "gangrene; pulpal", "Necrosis of pulp", "necrosis of pulp", "Devitalised pulp", "Putrescent pulpitis", "dental pulp necrosis", "Dental Pulp Necrosis", "Necrosis of the pulp", "necrosis of the pulp", "Dental Pulp Gangrene", "Dental Pulp Necroses", "Necroses, Dental Pulp", "Pulp Necroses, Dental", "Pulp Gangrene, Dental", "Gangrene, Dental Pulp", "Necrosis, Dental Pulp", "Pulp Necrosis, Dental", "necrosis; pulp (dental)", "pulp (dental); necrosis", "necrosis of pulp (diagnosis)", "Necrosis of the pulp (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dental pulp necrosis", "shortest_name_length": 9}
{"curie": "MONDO:0010252", "names": ["Mental Retardation, X-Linked, With Panhypopituitarism", "mental retardation, X-linked, with panhypopituitarism", "MENTAL RETARDATION, X-LINKED, WITH PANHYPOPITUITARISM", "intellectual disability, X-linked, with panhypopituitarism", "mental retardation, X-linked, with isolated Growth hormone deficiency", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, WITH PANHYPOPITUITARISM", "intellectual disability, X-linked, with isolated Growth hormone deficiency", "intellectual developmental disorder, X-linked, with isolated growth hormone deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked, with panhypopituitarism", "shortest_name_length": 53}
{"curie": "MONDO:0016778", "names": ["accidental botulism", "Iatrogenic Botulism", "Iatrogenic botulism", "iatrogenic botulism", "Accidental Botulism", "inadvertent botulism", "Inadvertent botulism", "Iatrogenic infection caused by Clostridium botulinum", "Iatrogenic infection caused by Clostridium botulinum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "iatrogenic botulism", "shortest_name_length": 19}
{"curie": "MONDO:0013156", "names": ["MDDGB4", "congenital muscular dystrophy-FKTN related", "congenital muscular dystrophy FKTN-related", "muscular dystrophy, congenital, Fktn-related", "MUSCULAR DYSTROPHY, CONGENITAL, FKTN-RELATED", "muscular dystrophy-dystroglycanopathy type B4", "muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type B, 4", "muscular dystrophy-dystroglycanopathy (congenital without intellectual disability), type B4", "muscular dystrophy-dystroglycanopathy (congenital without intellectual disability), type B, 4", "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT), TYPE B, 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy-dystroglycanopathy (congenital without intellectual disability), type B4", "shortest_name_length": 6}
{"curie": "UMLS:C4528212", "names": ["Type D LyP", "Type D Lymphomatoid Papulosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Type D Lymphomatoid Papulosis", "shortest_name_length": 10}
{"curie": "MONDO:0008514", "names": ["SD3", "SDTY3", "Sdty3", "syndactyly type 3", "Syndactyly type 3", "syndactyly, type 3", "Syndactyly, type 3", "Syndactyly, Type III", "SYNDACTYLY, TYPE III", "syndactyly, type III", "Familial syndactyly type 3", "Syndactyly type 3 (disorder)", "GJA1 non-syndromic syndactyly", "syndactyly of fingers 4 and 5", "Syndactyly of fingers 4 and 5", "SYNDACTYLY OF FINGERS IV AND V", "Syndactyly Of Fingers IV and V", "ringand little finger syndactyly", "Ring and little finger syndactyly", "RING AND LITTLE FINGER SYNDACTYLY", "Ring and Little finger syndactyly", "syndactyly of fingers four and five", "Syndactyly of fingers four and five", "syndactyly of the ring and little finger", "Syndactyly of the ring and little finger", "non-syndromic syndactyly caused by mutation in GJA1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndactyly type 3", "shortest_name_length": 3}
{"curie": "UMLS:C4727834", "names": ["Polystotic Langerhans cell histiocytosis", "Polyostotic Langerhans cell histiocytosis", "Langerhans Cell Histiocytosis, Polyostotic", "Langerhans cell histiocytosis, poly-ostotic", "Polyostotic Langerhans cell histiocytosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Polyostotic Langerhans cell histiocytosis", "shortest_name_length": 40}
{"curie": "UMLS:C0413252", "names": ["hypothermia", "Hypothermia", "hypothermia (diagnosis)", "Hypothermia due to exposure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypothermia due to exposure", "shortest_name_length": 11}
{"curie": "MONDO:0007287", "names": ["CTRCT41", "CATARACT 41", "cataract 41", "cataract type 41", "congenital nuclear type cataract 41", "cataract 41, congenital nuclear type", "CATARACT 41, CONGENITAL NUCLEAR TYPE", "WFS1 early-onset non-syndromic cataract", "early-onset non-syndromic cataract caused by mutation in WFS1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 41", "shortest_name_length": 7}
{"curie": "OMIM:110800", "names": ["Adult i phenotype", "i adult phenotype", "ADULT i PHENOTYPE", "i>adult< phenotype", "i<sub>adult</sub> phenotype", "i adult phenotype (finding)", "i>adult< phenotype (finding)", "i<sub>adult</sub> phenotype (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 17}
{"curie": "UMLS:C4763430", "names": ["Refractory Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Neuroendocrine Neoplasm", "shortest_name_length": 34}
{"curie": "UMLS:C1520096", "names": ["Vulvar Squamous Cell Carcinoma with Tumor Giant Cells"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Squamous Cell Carcinoma with Tumor Giant Cells", "shortest_name_length": 53}
{"curie": "MONDO:0019501", "names": ["ush", "USH", "RP8, FORMERLY", "Usher syndrome", "RP21, FORMERLY", "Usher Syndrome", "usher syndrome", "syndrome usher", "syndrome ushers", "Ushers Syndrome", "Syndrome, Usher", "syndromes usher", "Usher Syndromes", "syndrome usher's", "Usher's syndrome", "Usher's Syndrome", "Syndromes, Usher", "usher's syndrome", "Hallgren syndrome", "hallgren syndrome", "Syndrome, Usher's", "Hallgren Syndrome", "Syndrome, Hallgren", "Usher syndrome (US)", "Hallgren's syndrome", "Graefe-Usher Syndrome", "Graefe Usher Syndrome", "Graefe-Usher syndrome", "Syndrome, Graefe-Usher", "Usher syndrome (diagnosis)", "RETINITIS PIGMENTOSA 8, FORMERLY", "RETINITIS PIGMENTOSA 21, FORMERLY", "retinitis pigmentosa-deafness syndrome", "Retinitis Pigmentosa-Deafness Syndrome", "Deafness-Retinitis Pigmentosa Syndrome", "Retinitis Pigmentosa Deafness Syndrome", "Deafness-retinitis pigmentosa syndrome", "Retinitis pigmentosa-deafness syndrome", "RETINITIS PIGMENTOSA-DEAFNESS SYNDROME", "Deafness Retinitis Pigmentosa Syndrome", "dystrophia retinae-dysacousis syndrome", "deafness-retinitis pigmentosa syndrome", "Syndrome, Retinitis Pigmentosa-Deafness", "Syndrome, Deafness-Retinitis Pigmentosa", "Retinitis Pigmentosa-Deafness Syndromes", "Deafness-Retinitis Pigmentosa Syndromes", "Syndromes, Retinitis Pigmentosa-Deafness", "Pigmentosa Syndromes, Deafness-Retinitis", "Syndromes, Deafness-Retinitis Pigmentosa", "Retinitis pigmentosa-hearing loss syndrome", "Retinitis pigmentosa-deafness-ataxia syndrome", "retinitis pigmentosa-congenital deafness syndrome", "Dystrophia Retinae Pigmentosa-Dysostosis Syndrome", "dystrophia retinae pigmentosa-dysostosis syndrome", "Dystrophia Retinae Pigmentosa Dysostosis Syndrome", "Retinitis pigmentosa-deafness syndrome (disorder)", "dystrophia retinae pigmentosa-dysostosis syndrome (DRD)", "Retinitis pigmentosa-deafness-ataxia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Usher syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C0085183", "names": ["Second Neoplasm", "Neoplasm, Second", "Second Neoplasms", "second malignancy", "Neoplasms, Second", "Second Malignancy", "malignancy second", "Malignancy, Second", "second malignancies", "Second Malignancies", "Malignancies, Second", "Metachronous Neoplasm", "Metachronous Neoplasms", "Neoplasm, Metachronous", "Second Primary Neoplasm", "Neoplasms, Metachronous", "Second Primary Neoplasms", "Neoplasm, Second Primary", "Neoplasms, Second Primary", "Metachronous Second Primary Neoplasms", "Second Primary Neoplasms, Metachronous", "Neoplasms, Metachronous Second Primary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplasms, Second Primary", "shortest_name_length": 15}
{"curie": "MONDO:0010289", "names": ["MRX72", "XLID72", "X-linked mental retardation 72", "mental retardation, X-linked 72", "Mental Retardation, X-Linked 72", "MENTAL RETARDATION, X-LINKED 72", "mental retardation, X-linked type 72", "intellectual disability, X-linked 72", "intellectual disability, X-linked type 72", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 72", "non-syndromic X-linked intellectual disability 72", "intellectual developmental disorder, X-linked 72, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 72", "shortest_name_length": 5}
{"curie": "MONDO:0020677", "names": ["sudden hearing loss disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sudden hearing loss disorder", "shortest_name_length": 28}
{"curie": "MONDO:0009425", "names": ["HYPOMANDIBULAR FACIOCRANIAL DYSOSTOSIS", "Hypomandibular faciocranial dysostosis", "hypomandibular faciocranial dysostosis", "Hypomandibular faciocranial dysostosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypomandibular faciocranial dysostosis", "shortest_name_length": 38}
{"curie": "MONDO:0027068", "names": ["MC1DM1", "mitochondrial type mitochondrial complex I deficiency 1", "mitochondrial complex 1 deficiency, mitochondrial type 1", "mitochondrial complex I deficiency, mitochondrial type 1", "MITOCHONDRIAL COMPLEX I DEFICIENCY, MITOCHONDRIAL TYPE 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, mitochondrial type 1", "shortest_name_length": 6}
{"curie": "MONDO:0017507", "names": ["thumb hypodactyly, bilateral", "thumb oligodactyly, bilateral", "congenital absence/hypoplasia of thumb, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital absence/hypoplasia of thumb, bilateral", "shortest_name_length": 28}
{"curie": "UMLS:C1272516", "names": ["Small cell glioblastoma", "Small Cell Glioblastoma", "Small-cell glioblastoma", "Small cell glioblastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small cell glioblastoma", "shortest_name_length": 23}
{"curie": "UMLS:C5237191", "names": ["Refractory Pancreatic Ductal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Pancreatic Ductal Adenocarcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0005845", "names": ["Cerebromeningitis", "Cerebromeningitides", "Meningoencephalitis", "meningoencephalitis", "encephalomeningitis", "Encephalomeningitis", "MENINGOENCEPHALITIS", "Meningoencephalitides", "Encephalomeningitides", "Meningoencephalitis (disorder)", "meningoencephalitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "meningoencephalitis", "shortest_name_length": 17}
{"curie": "MONDO:0020049", "names": ["autosomal anomaly", "autosome chromosomal anomaly", "chromosomal anomaly of autosome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal anomaly", "shortest_name_length": 17}
{"curie": "UMLS:C1720796", "names": ["asymptomatic inflammatory prostatitis", "Asymptomatic Inflammatory Prostatitis", "Inflammatory Prostatitis, Asymptomatic", "Asymptomatic Inflammatory Prostatitides"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Asymptomatic Inflammatory Prostatitis", "shortest_name_length": 37}
{"curie": "MONDO:0009439", "names": ["NCIE", "NCIE1", "ARCI2", "NBCIE", "NCIE1, FORMERLY", "collodion baby, self-healing", "Autosomal Recessive Congenital Ichthyosis 2", "autosomal recessive congenital ichthyosis 2", "ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2", "ichthyosis, congenital, autosomal recessive 2", "autosomal recessive congenital ichthyosis type 2", "ichthyosis, congenital, autosomal recessive type 2", "nonbullous congenital ichthyosiform erythroderma 1", "ichthyosiform erythroderma, nonbullous congenital, 1", "ichthyosiform erythroderma, congenital, nonbullous, 1", "BROCQ congenital ichthyosiform erythroderma nonbullous form", "Brocq congenital ichthyosiform erythroderma nonbullous form", "ichthyosiform erythroderma, Brocq congenital, nonbullous form", "ichthyosiform erythroderma, nonbullous congenital, 1, formerly", "ICHTHYOSIFORM ERYTHRODERMA, NONBULLOUS CONGENITAL, 1, FORMERLY", "ICHTHYOSIFORM ERYTHRODERMA, BROCQ CONGENITAL, NONBULLOUS FORM, FORMERLY", "ichthyosiform erythroderma, Brocq congenital, nonbullous form, formerly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive congenital ichthyosis 2", "shortest_name_length": 4}
{"curie": "MONDO:0017373", "names": ["Polio", "polio", "Polia", "POLIO", "polios", "Polios", "Polio acute", "POLIO ACUTE", "Heine-Medin", "acute polio", "POLIOMYELITIS", "Poliomyelitis", "poliomyelitis", "Poliomyelitis NOS", "PM - Poliomyelitis", "Poliomyelitis, NOS", "HEINE-MEDIN DISEASE", "Acute poliomyelitis", "Acute Poliomyelitis", "infantile paralysis", "Heine-Medin disease", "acute poliomyelitis", "Poliomyelitis acute", "Poliomyelitis, Acute", "Poliomyelitis (acute)", "Poliomyelitis Infection", "Poliomyelitis Infections", "Acute poliomyelitis, NOS", "Infection, Poliomyelitis", "poliomyelitis (diagnosis)", "Infections, Poliomyelitis", "Epidemic acute poliomyelitis", "Epidemic Acute Poliomyelitis", "Acute Poliomyelitis, Epidemic", "Poliomyelitis, Epidemic Acute", "Acute poliomyelitis (disorder)", "Acute unspecified poliomyelitis", "Acute poliomyelitis, unspecified", "Epidemic acute poliomyelitis, NOS", "Epidemic acute poliomyelitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "poliomyelitis", "shortest_name_length": 5}
{"curie": "MONDO:0013782", "names": ["PHA2E", "Pseudohypoaldosteronism type 2E", "pseudohypoaldosteronism type 2E", "pseudohypoaldosteronism, type 2E", "pseudohypoaldosteronism, type IIE", "PSEUDOHYPOALDOSTERONISM, TYPE IIE", "Cul3 pseudohypoaldosteronism type 2", "CUL3 pseudohypoaldosteronism type 2", "pseudohypoaldosteronism type 2 caused by mutation in CUL3", "pseudohypoaldosteronism type 2 caused by mutation in Cul3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudohypoaldosteronism type 2E", "shortest_name_length": 5}
{"curie": "MONDO:0054832", "names": ["PPCD4", "posterior polymorphous corneal dystrophy 4", "corneal dystrophy, posterior polymorphous, 4", "corneal dystrophy, POSTERIOR polymorphous, 4", "CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal dystrophy, posterior polymorphous, 4", "shortest_name_length": 5}
{"curie": "UMLS:C5190713", "names": ["Hodgkin Lymphoma PTLD", "Hodgkin's Lymphoma PTLD", "Classical Hodgkin Lymphoma Type PTLD", "Hodgkin Lymphoma Post-Transplant Lymphoproliferative Disorder", "Hodgkin's Lymphoma Post-Transplant Lymphoproliferative Disorder", "Classical Hodgkin Lymphoma Post-Transplant Lymphoproliferative Disorder", "Classic Hodgkin Lymphoma Type Post-Transplant Lymphoproliferative Disorder", "Classical Hodgkin lymphoma type posttransplant lymphoproliferative disorder", "Classical Hodgkin lymphoma type post-transplant lymphoproliferative disorder", "Classical Hodgkin Lymphoma Type Post-Transplant Lymphoproliferative Disorder", "Classical Hodgkin lymphoma type post-transplant lymphoproliferative disorder (diagnosis)", "Classical Hodgkin lymphoma type posttransplant lymphoproliferative disorder (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Classical Hodgkin lymphoma type posttransplant lymphoproliferative disorder", "shortest_name_length": 21}
{"curie": "MONDO:0002646", "names": ["Laryngitis viral", "Viral laryngitis", "viral laryngitis", "Viral Laryngitis", "Viruses laryngitis", "Laryngitis viral NOS", "Viruses caused laryngitis", "viral laryngitis (diagnosis)", "Inflammation of larynx due to virus", "Inflammation of larynx caused by virus", "Inflammation of larynx caused by virus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "viral laryngitis", "shortest_name_length": 16}
{"curie": "MONDO:0008925", "names": ["CTRCT46", "Cataract Hutterite type", "cataract Hutterite type", "Hutterite type cataract", "cataract 46 juvenile-onset", "cataract 46, juvenile-onset", "cataract, congenital or juvenile", "juvenilae cataract Hutterite type", "Hutterite type cataract (disorder)", "CATARACT, JUVENILE, HUTTERITE TYPE", "cataract, juvenile, Hutterite type", "LEMD2 early-onset non-syndromic cataract", "early-onset non-syndromic cataract caused by mutation in LEMD2", "CATARACT 46, JUVENILE-ONSET, WITH OR WITHOUT ARRHYTHMIC CARDIOMYOPATHY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 46 juvenile-onset", "shortest_name_length": 7}
{"curie": "EFO:0009960", "names": ["atypical femoral fracture"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical femoral fracture", "shortest_name_length": 25}
{"curie": "UMLS:C0235987", "names": ["Virilism fetal", "VIRILISM FETAL", "Fetal Virilism", "Fetal virilism", "Virilism foetal", "VIRILISM FOETAL", "Foetal virilism", "Fetal Virilization", "Fetal virilism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fetal virilism", "shortest_name_length": 14}
{"curie": "UMLS:C0376634", "names": ["craniofacial anomaly", "anomalies craniofacial", "craniofacial abnormality", "Craniofacial Abnormality", "Abnormality, Craniofacial", "Craniofacial Abnormalities", "abnormalities craniofacial", "craniofacial abnormalities", "Abnormalities, Craniofacial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Craniofacial Abnormalities", "shortest_name_length": 20}
{"curie": "MONDO:0002581", "names": ["SCRMS", "Sclerosing rhabdomyosarcoma", "sclerosing rhabdomyosarcoma", "Sclerosing Rhabdomyosarcoma", "Spindle Cell Rhabdomyosarcoma", "spindle cell rhabdomyosarcoma", "Spindle cell rhabdomyosarcoma", "Spindle cell rhabdomyosarcoma (disorder)", "spindle cell rhabdomyosarcoma (diagnosis)", "Spindle cell rhabdomyosarcoma (morphologic abnormality)", "spindle cell rhabdomyosarcoma (morphologic abnormality)", "malignant neoplasm myosarcoma rhabdomyosarcoma spindle cell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spindle cell rhabdomyosarcoma", "shortest_name_length": 5}
{"curie": "MONDO:0019647", "names": ["congenital bilateral megacalycosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital bilateral megacalycosis", "shortest_name_length": 34}
{"curie": "UMLS:C4521719", "names": ["Stage IIIB Esophageal Adenocarcinoma", "Postneoadjuvant Therapy Stage IIIB Esophageal Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postneoadjuvant Therapy Stage IIIB Esophageal Adenocarcinoma AJCC v8", "shortest_name_length": 36}
{"curie": "UMLS:C5392105", "names": ["CRCI", "Chemo-Fog", "Chemo Fog", "Chemobrain", "Post-chemotherapy Cognitive Impairment", "Chemotherapy-Induced Cognitive Impairment", "Chemotherapy Induced Cognitive Impairment", "Chemotherapy Related Cognitive Impairment", "Chemotherapy-related Cognitive Impairment", "Chemotherapy-Related Cognitive Impairment", "Chemotherapy-Induced Cognitive Dysfunction", "Chemotherapy-Related Cognitive Impairments", "Cognitive Impairment, Chemotherapy-Induced", "Cognitive Impairment, Chemotherapy-Related", "Chemotherapy-related Cognitive Dysfunction", "Chemotherapy Induced Cognitive Impairments", "Chemotherapy Related Cognitive Dysfunction", "Chemotherapy Induced Cognitive Dysfunction", "Chemotherapy-Induced Cognitive Impairments", "Chemotherapy-Related Cognitive Dysfunction", "Cognitive Dysfunction, Chemotherapy-Related", "Cognitive Impairments, Chemotherapy-Induced", "Chemotherapy-Related Cognitive Dysfunctions", "Cognitive Dysfunction, Chemotherapy-Induced", "Cognitive Impairments, Chemotherapy-Related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chemotherapy-Related Cognitive Impairment", "shortest_name_length": 4}
{"curie": "MONDO:0033485", "names": ["SRTD19", "short-rib thoracic dysplasia 19 with or without polydactyly", "SHORT-RIB THORACIC DYSPLASIA 19 WITH OR WITHOUT POLYDACTYLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short-rib thoracic dysplasia 19 with or without polydactyly", "shortest_name_length": 6}
{"curie": "MONDO:0016769", "names": ["llp", "Linear LP", "linear LP", "Blaschkoid LP", "Linear lichen planus", "linear lichen planus", "Lichen planus, linear", "Lichen planus linearis", "lichen planus linearis", "Blaschkoid lichen planus", "Linear lichen planus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "linear lichen planus", "shortest_name_length": 3}
{"curie": "MONDO:0001093", "names": ["Colon Lymphangioma", "colon lymphangioma", "Colonic Lymphangioma", "colonic lymphangioma", "Lymphangioma of Colon", "Lymphangioma of colon", "lymphangioma of colon", "lymphangioma of the colon", "Lymphangioma of the Colon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colonic lymphangioma", "shortest_name_length": 18}
{"curie": "MONDO:0020571", "names": ["relapsing epidemic typhus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "relapsing epidemic typhus", "shortest_name_length": 25}
{"curie": "MONDO:0009267", "names": ["GD3", "Gd 3", "GD III", "Type 3 Gaucher Disease", "Gaucher Disease Type 3", "Gaucher disease type 3", "Gaucher disease, type 3", "Gaucher Disease, Type 3", "Gaucher disease type III", "Gaucher disease, type 3B", "Juvenile Gaucher disease", "Gaucher disease, type 3A", "Juvenile Gaucher Disease", "Gaucher Disease, Juvenile", "Disease, Juvenile Gaucher", "Gaucher disease, type III", "Gaucher Disease, Type III", "GAUCHER DISEASE, TYPE III", "GAUCHER DISEASE, TYPE IIIB", "GAUCHER DISEASE, TYPE IIIA", "Juvenile Gaucher's disease", "Gaucher's disease type III", "Gaucher Disease, Type IIIa", "gaucher's disease type iii", "type iii gaucher's disease", "Gaucher Disease, Type IIIb", "Gaucher's disease, type III", "Norrbottnian Gaucher disease", "Neuronopathic Gaucher Disease", "Gaucher Disease, Neuronopathic", "Disease, Neuronopathic Gaucher", "Gaucher Disease, Type 3 (disorder)", "GAUCHER DISEASE, NORRBOTTNIAN TYPE", "Gaucher disease, Norrbottnian type", "Gaucher Disease, Norrbottnian Type", "Gaucher disease type III (diagnosis)", "Chronic neuronopathic Gaucher disease", "chronic neuronopathic Gaucher disease", "subacute neuronopathic gaucher disease", "Subacute Neuronopathic Gaucher Disease", "Subacute neuronopathic Gaucher disease", "Glucocerebrosidase deficiency type III", "Subacute neuronopathic Gaucher's disease", "GAUCHER DISEASE, CHRONIC NEURONOPATHIC TYPE", "Gaucher disease, chronic neuronopathic type", "Gaucher Disease, Chronic Neuronopathic Type", "Gaucher Disease, Subacute Neuronopathic Type", "Glucosylceramidase deficiency, subacute type", "GAUCHER DISEASE, SUBACUTE NEURONOPATHIC TYPE", "Gaucher disease, subacute neuronopathic type", "Gaucher Disease, Subacute Neuronopathic Form", "Gaucher disease, Subacute neuronopathic type", "Gaucher disease, juvenile and adult, cerebral", "GAUCHER DISEASE, JUVENILE AND ADULT, CEREBRAL", "Gaucher Disease, Juvenile and Adult, Cerebral", "Gaucher Disease, Juvenile And Adult, Cerebral", "Subacute neuronopathic Gaucher's disease (disorder)", "cerebral juvenile and adult form of Gaucher disease", "Cerebral juvenile and adult form of Gaucher disease", "Gaucher's disease III, adult form or juvenile, (cerebral)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gaucher disease type III", "shortest_name_length": 3}
{"curie": "UMLS:C0278556", "names": ["Anal cancer recurrent", "recurrent anal cancer", "Recurrent Anal Cancer", "recurrent anus cancer", "anus cancer, recurrent", "anal cancer, recurrent", "Anal canal cancer recurrent", "Recurrent Anal Canal Cancer", "Recurrent Anal Canal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anal cancer recurrent", "shortest_name_length": 21}
{"curie": "MONDO:0012690", "names": ["NS5", "Noonan Syndrome 5", "NOONAN SYNDROME 5", "Noonan syndrome 5", "RAF1 Noonan syndrome", "Noonan syndrome type 5", "RAF1 gene related Noonan syndrome", "Noonan syndrome caused by mutation in RAF1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Noonan syndrome 5", "shortest_name_length": 3}
{"curie": "MONDO:0006736", "names": ["Cervix Dysplasia", "cervix dysplasia", "dysplasia; cervix", "Dysplasia, Cervix", "cervix; dysplasia", "Dysplasia;cervical", "cervical precancer", "Cervical dysplasia", "CERVICAL DYSPLASIA", "Cervical Dysplasia", "cervical dysplasia", "Dysplasia of cervix", "Cervical Dysplasias", "dysplasia of cervix", "Dysplasia, Cervical", "Cervix Uteri Dysplasia", "Cervical dysplasia NOS", "Cervix Uteri Dysplasias", "Uterine cervix dysplasia", "Dysplasia of Cervix Uteri", "Dysplasia of cervix uteri", "Uterine Cervical Dysplasia", "Dysplasia, Uterine Cervical", "Cervical Dysplasia, Uterine", "Dysplasia of cervix (uteri)", "Dysplasia of cervix (disorder)", "Dysplasia of cervix, unspecified", "Cervical Intraepithelial Neoplasm", "Neoplasm, Cervical Intraepithelial", "Cervical Intraepithelial Neoplasia", "Cervical Intraepithelial Neoplasms", "Intraepithelial Neoplasm, Cervical", "Neoplasms, Cervical Intraepithelial", "Intraepithelial Neoplasms, Cervical", "Neoplasia, Cervical Intraepithelial", "Intraepithelial Neoplasia, Cervical", "Dysplasia of cervix uteri, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dysplasia of cervix", "shortest_name_length": 16}
{"curie": "MONDO:0006924", "names": ["Bartonellaceae Infection", "Bartonellaceae infection", "Infection, Bartonellaceae", "Bartonellaceae Infections", "infection, Bartonellaceae", "infections, Bartonellaceae", "Infections, Bartonellaceae", "Bartonellaceae infectious disease", "Bartonellaceae disease or disorder", "primary Bartonellaceae infectious disease", "Bartonellaceae caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bartonellaceae infectious disease", "shortest_name_length": 24}
{"curie": "UMLS:C0019086", "names": ["hemorrhagic ascites", "Hemorrhagic ascites", "Hemorrhagic Ascites", "Haemorrhagic ascites", "Hemorrhagic ascites (disorder)", "Hemorrhagic peritoneal effusion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemorrhagic ascites", "shortest_name_length": 19}
{"curie": "UMLS:C4524737", "names": ["Pathologic Stage IIIA Gastroesophageal Junction Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IIIA Gastroesophageal Junction Adenocarcinoma AJCC v8", "shortest_name_length": 70}
{"curie": "MONDO:0013880", "names": ["HCFP3", "facial paresis, hereditary congenital, 3", "FACIAL PARESIS, HEREDITARY CONGENITAL, 3", "facial paresis, hereditary congenital, type 3", "HOXB1 congenital hereditary facial paralysis-variable hearing loss syndrome", "congenital hereditary facial paralysis-variable hearing loss syndrome caused by mutation in HOXB1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "facial paresis, hereditary congenital, 3", "shortest_name_length": 5}
{"curie": "MONDO:0016350", "names": ["Daentl Towsend Siegel syndrome", "Daentl-Townsend-Siegel syndrome", "hydrocephalus blue sclera nephropathy", "Hydrocephalus blue sclera nephropathy", "hydrocephalus-blue sclerae-nephropathy syndrome", "Familial nephrosis, hydrocephalus, thin skin, blue sclerae syndrome", "familial nephrosis, hydrocephalus, thin skin, blue sclerae syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hydrocephalus-blue sclerae-nephropathy syndrome", "shortest_name_length": 30}
{"curie": "MONDO:0011398", "names": ["DEB-Pr", "DEB pruriginosa", "DEB, PRURIGINOSA", "DEB, pruriginosa", "Deb, pruriginosa", "EPIDERMOLYSIS BULLOSA PRURIGINOSA", "Epidermolysis bullosa pruriginosa", "epidermolysis bullosa pruriginosa", "Epidermolysis Bullosa Pruriginosa", "dystrophic epidermolysis bullosa pruriginosa", "Epidermolysis bullosa pruriginosa (disorder)", "DYSTROPHIC EPIDERMOLYSIS BULLOSA PRURIGINOSA", "Dystrophic epidermolysis bullosa pruriginosa", "Dystrophic Epidermolysis Bullosa Pruriginosa", "Pruriginous dystrophic epidermolysis bullosa", "pruriginous dystrophic epidermolysis bullosa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dystrophic epidermolysis bullosa pruriginosa", "shortest_name_length": 6}
{"curie": "UMLS:C0855223", "names": ["Hallucinations, mixed"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hallucinations, mixed", "shortest_name_length": 21}
{"curie": "MONDO:0026729", "names": ["CDG1CC", "congenital disorder of glycosylation Icc", "congenital disorder of glycosylation type Icc", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Icc", "congenital disorder of glycosylation, type ICC", "congenital disorder of glycosylation, type Icc, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital disorder of glycosylation, type ICC", "shortest_name_length": 6}
{"curie": "UMLS:C4687508", "names": ["Stage III Malignant Thymic Germ Cell Tumor", "Stage III Malignant Mediastinal Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Malignant Mediastinal Germ Cell Tumor", "shortest_name_length": 42}
{"curie": "MONDO:0035402", "names": ["isolated exencephaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated exencephaly", "shortest_name_length": 20}
{"curie": "MONDO:0012358", "names": ["LPRS1", "LEPROSY, SUSCEPTIBILITY TO, 1", "leprosy, susceptibility to, 1", "leprosy, paucibacillary type, susceptibility to", "LEPROSY, PAUCIBACILLARY TYPE, SUSCEPTIBILITY TO, 1", "leprosy, Paucibacillary type, susceptibility to, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leprosy, susceptibility to, 1", "shortest_name_length": 5}
{"curie": "MONDO:0003486", "names": ["basaloid carcinoma", "Basaloid carcinoma", "basaloid squamous cell carcinoma", "Basaloid squamous cell carcinoma", "Basaloid Squamous Cell Carcinoma", "basaloid squamous cell carcinoma (diagnosis)", "basaloid carcinoma (morphologic abnormality)", "basaloid squamous cell carcinoma (morphologic abnormality)", "Basaloid squamous cell carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "basaloid squamous cell carcinoma", "shortest_name_length": 18}
{"curie": "MONDO:0003199", "names": ["Ca anus", "anal cancer", "Anal Cancer", "Anal cancer", "ANAL CANCER", "Anus Cancer", "anus cancer", "Anus--Cancer", "Anus Cancers", "Cancer, Anal", "Anal Cancers", "Cancers, Anal", "anal carcinoma", "Anal carcinoma", "Cancer of Anus", "anus carcinoma", "cancer of anus", "Anal Carcinoma", "Carcinoma;anus", "Anal cancer, NOS", "carcinoma of anus", "Carcinoma of Anus", "Carcinoma of anus", "Cancer of the Anus", "cancer of the anus", "Anal carcinoma NOS", "Carcinoma of the Anus", "carcinoma of the anus", "Anal Cancer (all types)", "anus carcinoma epidermoid", "anus carcinoma cell squamous", "squamous cell carcinoma anus", "carcinoma of anus (diagnosis)", "Metastatic anal adenocarcinoma", "Malignant epithelial neoplasm of anus", "Malignant epithelial neoplasm of anus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anal carcinoma", "shortest_name_length": 7}
{"curie": "MONDO:0011679", "names": ["autosomal recessive craniosynostosis", "craniosynostosis, autosomal recessive", "Craniosynostosis Syndrome, Autosomal Recessive", "craniosynostosis syndrome, autosomal recessive", "CRANIOSYNOSTOSIS SYNDROME, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniosynostosis syndrome, autosomal recessive", "shortest_name_length": 36}
{"curie": "MONDO:0016161", "names": ["cerebral gigantism jaw cysts", "Cramer Niederdellmann syndrome", "Cramer-Niederdellmann syndrome", "cerebral gigantism-jaw cysts syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral gigantism-jaw cysts syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0015795", "names": ["UES", "Embryonal Sarcoma", "Liver Embryonal Sarcoma", "Undifferentiated Sarcoma", "embryonal sarcoma of liver", "Embryonal sarcoma of liver", "Embryonal Sarcoma of the Liver", "Embryonal sarcoma of the liver", "embryonal sarcoma of the liver", "undifferentiated sarcoma of liver", "Undifferentiated (Embryonal) Sarcoma", "Undifferentiated sarcoma of the liver", "undifferentiated sarcoma of the liver", "Embryonal sarcoma of liver (disorder)", "embryonal sarcoma of liver (diagnosis)", "Embryonal Sarcoma (Undifferentiated Sarcoma)", "undifferentiated sarcoma of liver (diagnosis)", "Undifferentiated embryonal sarcoma of the liver", "undifferentiated embryonal sarcoma of the liver", "Undifferentiated (Embryonal) Sarcoma of the Liver"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "undifferentiated embryonal sarcoma of the liver", "shortest_name_length": 3}
{"curie": "UMLS:C4331326", "names": ["Stage III Hypopharyngeal Throat Cancer", "Stage III Hypopharyngeal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Hypopharyngeal Carcinoma AJCC v8", "shortest_name_length": 38}
{"curie": "UMLS:C0854803", "names": ["Stage II CLL", "CLL Stage II", "CLL, stage II", "Chronic lymphocytic leukemia stage 2", "stage II chronic lymphocytic leukemia", "Stage II Chronic Lymphocytic Leukemia", "Chronic lymphocytic leukaemia stage 2", "Chronic Lymphocytic Leukemia Stage II", "leukemia, stage II chronic lymphocytic", "lymphocytic leukemia, stage II chronic", "chronic lymphocytic leukemia, stage II", "Stage II Chronic Lymphocytic Leukemia (CLL)", "Stage II Chronic Lymphocytic Leukemia- Modified Rai Staging System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic lymphocytic leukemia stage 2", "shortest_name_length": 12}
{"curie": "MONDO:0005555", "names": ["cyclopegia", "Cyclopegia", "CYCLOPLEGIA", "Cycloplegia", "cycloplegia", "accommodative paresis", "Loss of accommodation", "Accommodative paresis", "loss of accommodation", "Ciliary muscle paresis", "ciliary muscle paresis", "Cycloplegia (disorder)", "ACCOMMODATION PARALYSIS", "Accommodation paralysis", "paresis of accommodation", "paralysis; accommodation", "accommodations paralysis", "accommodation; paralysis", "Paresis of accommodation", "paralysis of accommodation", "Paralysis of accommodation", "Visual accommodation paralysis", "visual accommodation paralysis", "paresis of accommodation (diagnosis)", "Cycloplegic paralysis of accommodation", "cycloplegic paralysis of accommodation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cycloplegia", "shortest_name_length": 10}
{"curie": "MONDO:0004496", "names": ["MYOCARDITIS", "myocarditis", "Myocarditis", "MYOCARDITIDES", "Myocarditides", "Myocarditis NOS", "Myocarditis, NOS", "Myocarditis (disorder)", "myocardial inflammation", "myocardium inflammation", "Myocardial inflammation", "myocarditis (diagnosis)", "inflammation; myocardium", "myocardium; inflammation", "Myocarditis, unspecified", "inflammation of myocardium", "Inflammation of heart muscle", "myocardial inflammation (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myocarditis", "shortest_name_length": 11}
{"curie": "MONDO:0030810", "names": ["PFIC10", "CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 10", "cholestasis, progressive familial intrahepatic, 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholestasis, progressive familial intrahepatic, 10", "shortest_name_length": 6}
{"curie": "MONDO:0025013", "names": ["Primate Disease", "primate disease", "Primate disease", "Disease, Primate", "Primate Diseases", "disease, Primate", "Diseases, Primate", "diseases, Primate", "diseases primates", "Primates--Diseases", "non-human primate disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-human primate disease", "shortest_name_length": 15}
{"curie": "UMLS:C0949857", "names": ["Respiratory Chain Deficiency", "Deficiency, Respiratory Chain", "Deficiencies, Respiratory Chain", "Mitochondrial Respiratory Chain Deficiencies", "Respiratory Chain Deficiencies, Mitochondrial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mitochondrial Respiratory Chain Deficiencies", "shortest_name_length": 28}
{"curie": "MONDO:0015999", "names": ["PPNAD", "pigmented nodular adrenocortical disease", "Primary Pigmented Nodular Adrenal Dysplasia", "primary pigmented nodular adrenal dysplasia", "Primary pigmented nodular adrenal dysplasia", "Primary pigmented nodular adrenocortical disease", "primary pigmented nodular adrenocortical disease", "pigmented nodular adrenocortical disease, primary", "Primary pigmented nodular adrenocortical disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary pigmented nodular adrenocortical disease", "shortest_name_length": 5}
{"curie": "MONDO:0010495", "names": ["TTD5", "nonphotosensitive trichothiodystrophy 5", "TRICHOTHIODYSTROPHY 5, NONPHOTOSENSITIVE", "trichothiodystrophy 5, nonphotosensitive", "RNF113A nonphotosensitive trichothiodystrophy", "nonphotosensitive trichothiodystrophy caused by mutation in RNF113A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichothiodystrophy 5, nonphotosensitive", "shortest_name_length": 4}
{"curie": "MONDO:0003602", "names": ["Brain Liposarcoma", "Intracranial Liposarcoma", "intracranial liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intracranial liposarcoma", "shortest_name_length": 17}
{"curie": "UMLS:C0854109", "names": ["Congenital Epilepsy", "Epilepsy congenital"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epilepsy congenital", "shortest_name_length": 19}
{"curie": "MONDO:0043678", "names": ["inv", "inversion", "Inversion", "genetic inversion", "Genetic inversion", "Inverted Chromosome", "inverted chromosome", "chromosome inversion", "Chromosome inversion", "Chromosome Inversion", "Chromosomal Inversion", "Inversion, Chromosome", "Chromosome inversions", "chromosome Inversions", "inversion, chromosome", "chromosome inversions", "Chromosome Inversions", "chromosomal inversion", "Inversions, Chromosome", "Chromosomal Inversions", "inversion, chromosomal", "chromosomal Inversions", "Inversions, chromosome", "Inversion, Chromosomal", "Inversions, chromosomal", "Inversions, Chromosomal", "Chromosome inversion, NOS", "Genetic inversion (finding)", "chromosome inversion disorder", "Chromosome inversion (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome inversion disorder", "shortest_name_length": 3}
{"curie": "MONDO:0019202", "names": ["MFS", "Myxoid MFH", "myxoid MFH", "Myxoid DFSP", "DFSP, Myxoid", "Myxoid DFSPs", "DFSPs, Myxoid", "myxofibrosarcoma", "Fibromyxosarcoma", "Myxofibrosarcoma", "fibromyxosarcoma", "fibromyxoid sarcoma", "Myxoid dermatofibrosarcoma", "myxoid fibrous histiocytoma", "fibromyxosarcoma (diagnosis)", "Myxoid Dermatofibrosarcoma Protuberan", "myxoid malignant fibrous histiocytoma", "Myxoid Malignant Fibrous Histiocytoma", "Myxoid malignant fibrous histiocytoma", "Myxoid Dermatofibrosarcoma Protuberans", "Myxoid dermatofibrosarcoma protuberans", "Dermatofibrosarcoma Protuberan, Myxoid", "Protuberan, Myxoid Dermatofibrosarcoma", "Protuberans, Myxoid Dermatofibrosarcoma", "Dermatofibrosarcoma Protuberans, Myxoid", "Myxofibrosarcoma (morphologic abnormality)", "Fibromyxosarcoma (morphologic abnormality)", "Myxoid dermatofibrosarcoma protuberans (disorder)", "soft tissue dermatofibrosarcoma protuberans myxoid", "Myxoid dermatofibrosarcoma protuberans (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myxofibrosarcoma", "shortest_name_length": 3}
{"curie": "MONDO:0018433", "names": ["AML with t(6;9)(p23;q34)", "acute myeloid leukemia with t(6;9)(p23;q34)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia with t(6;9)(p23;q34)", "shortest_name_length": 24}
{"curie": "MONDO:0005395", "names": ["movement disease", "Unusual movement", "Movement disorder", "Movement Disorder", "movement disorder", "Unusual movements", "MOVEMENT DISORDER", "Movement Disorders", "MOVEMENT DISORDERS", "movement disorders", "Movement disorders", "movement; disorder", "disorder; movement", "Dyskinesia Syndrome", "Dyskinesia syndrome", "DYSKINESIA SYNDROME", "Dyskinesia Syndromes", "Movement disorder NOS", "Movement abnormalities", "Movement disorder, NOS", "Abnormality of movement", "MOVEMENT DISORDER (NOS)", "Movements disturbance NOS", "Movement Disorder Syndrome", "Movement Disorder Syndromes", "Movement disorder (disorder)", "movement disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "movement disorder", "shortest_name_length": 16}
{"curie": "UMLS:C4682560", "names": ["Stage IIIA Uterine Corpus Leiomyosarcoma", "Stage IIIA Uterine Corpus Leiomyosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Uterine Corpus Leiomyosarcoma AJCC v8", "shortest_name_length": 40}
{"curie": "UMLS:C0393773", "names": ["Work shift change", "Work shift change (disorder)", "Shift Work Type Circadian Rhythm Sleep Disorder", "Circadian rhythm sleep disorder, shift work type", "sleep disorder circadian rhythm, shift work type", "Circadian rhythm sleep disorder, shift work type (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Work shift change (disorder)", "shortest_name_length": 17}
{"curie": "MONDO:0016315", "names": ["MPS2A", "MPSIIA", "Hunter syndrome type A", "Hunter syndrome, severe form", "Mucopolysaccharidosis type 2A", "mucopolysaccharidosis type 2A", "Mucopolysaccharidosis type IIA", "Hunter's syndrome, severe form", "mucopolysaccharidosis type IIA", "iduronate 2-sulfatase deficiency type A", "Iduronate 2-sulfatase deficiency type A", "mucopolysaccharidosis type 2, severe form", "Mucopolysaccharidosis type II severe form", "Hunter's syndrome, severe form (disorder)", "Mucopolysaccharidosis type 2, severe form", "mucopolysaccharidosis type II, severe form", "Mucopolysaccharidosis type II, severe form", "MUCOPOLYSACCHARIDOSIS, TYPE II, SEVERE FORM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucopolysaccharidosis type 2, severe form", "shortest_name_length": 5}
{"curie": "MONDO:0002878", "names": ["uterine adenosarcoma", "Uterine adenosarcoma", "adenosarcoma of uterus", "Adenosarcoma of uterus", "Uterine Body Adenosarcoma", "uterine body adenosarcoma", "adenosarcoma of the uterus", "Adenosarcoma of the uterus", "Body of Uterus Adenosarcoma", "body of uterus adenosarcoma", "Uterine Corpus Adenosarcoma", "uterine corpus adenosarcoma", "adenosarcoma of uterine body", "Adenosarcoma of Uterine Body", "Adenosarcoma of Uterine Corpus", "Adenosarcoma of Body of Uterus", "adenosarcoma of uterine corpus", "adenosarcoma of body of uterus", "adenosarcoma of the corpus uteri", "Adenosarcoma of the Uterine Body", "adenosarcoma of the uterine body", "Adenosarcoma of uterus (disorder)", "adenosarcoma of uterus (diagnosis)", "adenosarcoma of the body of uterus", "Adenosarcoma of the Body of Uterus", "Adenosarcoma of the Uterine Corpus", "adenosarcoma of the uterine corpus", "Mullerian adenosarcoma of the uterus", "uterine corpus Mullerian adenosarcoma", "uterine corpus Müllerian adenosarcoma", "uterine corpus mullerian adenosarcoma", "uterine Corpus mullerian adenosarcoma", "Uterine Corpus Müllerian Adenosarcoma", "Uterine Corpus Mullerian Adenosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine corpus adenosarcoma", "shortest_name_length": 20}
{"curie": "MONDO:0019923", "names": ["UPD(11)pat", "Mosaic paternal uniparental disomy of chromosome 11", "Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11", "Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome type 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11", "shortest_name_length": 10}
{"curie": "MONDO:0020649", "names": ["warty carcinoma of penis", "Warty Carcinoma of Penis", "Warty Carcinoma of the Penis", "warty carcinoma of the penis", "Condylomatous Carcinoma of Penis", "condylomatous carcinoma of penis", "Condylomatous Carcinoma of the Penis", "warty penile squamous cell carcinoma", "Warty Penile Squamous Cell Carcinoma", "condylomatous carcinoma of the penis", "Warty Squamous Cell Carcinoma of Penis", "warty squamous cell carcinoma of penis", "Warty Squamous Cell Carcinoma of the Penis", "warty squamous cell carcinoma of the penis", "Condylomatous Penile Squamous Cell Carcinoma", "Squamous Cell Carcinoma of Penis, Warty Type", "squamous cell carcinoma of penis, warty type", "condylomatous penile squamous cell carcinoma", "condylomatous squamous cell carcinoma of penis", "Condylomatous Squamous Cell Carcinoma of Penis", "Squamous Cell Carcinoma of the Penis, Warty Type", "squamous cell carcinoma of the penis, warty type", "condylomatous squamous cell carcinoma of the penis", "Condylomatous Squamous Cell Carcinoma of the Penis", "Squamous Cell Carcinoma of Penis, Condylomatous Type", "squamous cell carcinoma of penis, condylomatous type", "squamous cell carcinoma of the penis, condylomatous type", "Squamous Cell Carcinoma of the Penis, Condylomatous Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "warty carcinoma of the penis", "shortest_name_length": 24}
{"curie": "MONDO:0019452", "names": ["MPN-U", "CMPD-U", "MPN, U", "CMPD, U", "Myeloproliferative Neoplasm, Unclassifiable", "myeloproliferative neoplasm, unclassifiable", "undifferentiated myeloproliferative disease", "Unclassifiable Chronic Myeloproliferative Disease", "unclassifiable chronic myeloproliferative disease", "Chronic Myeloproliferative Disease, Unclassifiable", "unclassifiable chronic myeloproliferative disorder", "chronic myeloproliferative disease, unclassifiable", "Unclassifiable Chronic Myeloproliferative Disorder", "chronic myeloproliferative disorder, unclassifiable", "Chronic Myeloproliferative Disorder, Unclassifiable"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myeloproliferative neoplasm, unclassifiable", "shortest_name_length": 5}
{"curie": "MONDO:0015170", "names": ["Na-H exchange deficiency", "Congenital sodium diarrhea", "congenital sodium diarrhea", "Congenital sodium diarrhoea", "Non-syndromic congenital sodium diarrhea", "Non-syndromic congenital sodium diarrhoea", "Congenital secretory diarrhea, sodium type", "Congenital secretory diarrhoea, sodium type", "Defective Na+/H+ exchange in jejunum and ileum", "Defective Na+/H+ exchange in jejunum AND/OR ileum", "Congenital secretory diarrhea, sodium type (disorder)", "Defective Na^+^/H^+^ exchange in jejunum AND/OR ileum", "Defective Na<sup>+</sup>/H<sup>+</sup> exchange in jejunum AND/OR ileum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital sodium diarrhea", "shortest_name_length": 24}
{"curie": "MONDO:0100222", "names": ["HA20", "A20 haploinsufficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "A20 haploinsufficiency", "shortest_name_length": 4}
{"curie": "MONDO:0017197", "names": ["Whyte Murphy syndrome", "Whyte-Murphy syndrome", "Osteopathia striata-pigmentary dermopathy-white forelock syndrome", "osteopathia striata-pigmentary dermopathy-white forelock syndrome", "Osteopathia striata, pigmentary dermopathy, white forelock syndrome", "osteopathia striata with pigmentary dermopathy including white forelock", "Osteopathia striata associated with familial dermopathy and white forelock", "osteopathia striata associated with familial dermopathy and white forelock", "Osteopathia striata, pigmentary dermopathy, white forelock syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteopathia striata-pigmentary dermopathy-white forelock syndrome", "shortest_name_length": 21}
{"curie": "OMIM:305690", "names": ["GENITOURINARY TRACT ANOMALIES", "Genitourinary Tract Anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 29}
{"curie": "UMLS:C0264686", "names": ["Coronary embolus", "Coronary embolism", "CORONARY EMBOLISM", "EMBOLISM, CORONARY", "EMBOLUS CORONARY ARTERY", "Embolus coronary artery", "Embolism;artery;coronary", "Coronary artery embolism", "coronary artery embolism", "coronary (artery) embolism", "Coronary artery embolism (disorder)", "coronary artery embolism (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Coronary artery embolism", "shortest_name_length": 16}
{"curie": "UMLS:C4725671", "names": ["High-Risk Neuroblastoma", "High Risk Neuroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Risk Neuroblastoma", "shortest_name_length": 23}
{"curie": "UMLS:C2828206", "names": ["Stage IVA Bone Cancer", "Stage IVA Bone Cancer AJCC v7", "Stage IVA Bone Cancer  AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Bone Cancer AJCC v7", "shortest_name_length": 21}
{"curie": "MONDO:0008943", "names": ["CPD3", "CPD 3", "SCAR2", "CPDIII", "CPD III", "cerebelloparenchymal disorder 3", "CEREBELLOPARENCHYMAL DISORDER III", "Cerebelloparenchymal Disorder III", "Cerebelloparenchymal disorder III", "autosomal recessive spinocerebellar ataxia 2", "Spinocerebellar Ataxia Autosomal Recessive 2", "Spinocerebellar Ataxia, Autosomal Recessive 2", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2", "spinocerebellar ataxia, autosomal recessive 2", "CEREBELLAR HYPOPLASIA, NONPROGRESSIVE NORMAN TYPE", "autosomal recessive spinocerebellar ataxia type 2", "cerebellar hypoplasia, nonprogressive Norman type", "Autosomal recessive spinocerebellar ataxia type 2", "Cerebellar Hypoplasia, Nonprogressive Norman Type", "SCAR2 (spinocerebellar ataxia autosomal recessive 2)", "PMPCA autosomal recessive congenital cerebellar ataxia", "autosomal recessive cerebelloparenchymal disorder type 3", "Autosomal recessive cerebelloparenchymal disorder type 3", "Autosomal recessive cerebelloparenchymal disorder type 3 (disorder)", "Cerebellar Granular Cell Hypoplasia and Mental Retardation, Congenital", "CEREBELLAR GRANULAR CELL HYPOPLASIA AND MENTAL RETARDATION, CONGENITAL", "cerebellar granular cell hypoplasia and mental retardation, congenital", "cerebellar granular cell hypoplasia and intellectual disability, congenital", "autosomal recessive congenital cerebellar ataxia caused by mutation in PMPCA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive spinocerebellar ataxia 2", "shortest_name_length": 4}
{"curie": "MONDO:0008890", "names": ["bulbar palsy", "Bulbar Palsy", "Bulbar palsy", "BULBAR PALSY", "Palsy, Bulbar", "bulbar palsies", "Bulbar Palsies", "Bulbar palsies", "Bulbar weakness", "Palsies, Bulbar", "Paralysis bulbar", "Bulbar Paralyses", "PARALYSIS BULBAR", "Bulbar Paralysis", "bulbar paralysis", "Bulbar paralysis", "Paralysis, Bulbar", "paralysis; bulbar", "bulbar; paralysis", "Fazio-Londe disease", "Bulbar muscle weakness", "progressive bulbar palsy", "Progressive bulbar palsy", "bulbar palsy progressive", "Progressive Bulbar Palsy", "Palsy, Progressive Bulbar", "Bulbar Palsy, Progressive", "Progressive Bulbar Palsies", "Bulbar weakness (disorder)", "progressive bulbar atrophy", "Palsies, Progressive Bulbar", "Bulbar Palsies, Progressive", "PBP - Progressive bulbar palsy", "Progressive bulbar palsy (disorder)", "progressive bulbar palsy (diagnosis)", "bulbar palsy, progressive, of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive bulbar palsy", "shortest_name_length": 12}
{"curie": "UMLS:C0685629", "names": ["Short Supernumerary Rib", "Short supernumerary rib", "SUPERNUMERARY RIB, SHORT", "Short supernumerary rib (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Short supernumerary rib", "shortest_name_length": 23}
{"curie": "UMLS:C1333285", "names": ["Diencephalic GBM", "GBM of Diencephalon", "GBM of the Diencephalon", "Diencephalic Glioblastoma", "Diencephalic Glioblastoma Multiforme", "Glioblastoma Multiforme of Diencephalon", "Glioblastoma Multiforme of the Diencephalon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diencephalic Glioblastoma", "shortest_name_length": 16}
{"curie": "UMLS:C4727578", "names": ["Locally Advanced Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Squamous Cell Carcinoma", "shortest_name_length": 40}
{"curie": "UMLS:C2984094", "names": ["Breast Cancer by AJCC v7 Stage", "Breast Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Cancer by AJCC v7 Stage", "shortest_name_length": 30}
{"curie": "MONDO:0014802", "names": ["CWS7", "COWDEN SYNDROME 7", "Cowden syndrome 7", "SEC23B Cowden disease", "Cowden syndrome type 7", "Cowden disease caused by mutation in SEC23B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cowden syndrome 7", "shortest_name_length": 4}
{"curie": "MONDO:0002358", "names": ["Larynx Cancer", "cancer of larynx", "Carcinoma;larynx", "carcinoma larynx", "Laryngeal cancer", "Cancer of Larynx", "CARCINOMA LARYNX", "laryngeal cancer", "larynx carcinoma", "Carcinoma larynx", "LARNYX CARCINOMA", "Laryngeal Cancer", "Larynx Carcinoma", "Larynx carcinoma", "laryngeal carcinoma", "Laryngeal carcinoma", "CARCINOMA OF LARYNX", "Carcinoma of larynx", "LARYNGEAL CARCINOMA", "carcinoma of larynx", "Carcinoma of Larynx", "Laryngeal Carcinoma", "carcinoma laryngeal", "cancer of the larynx", "Cancer of the larynx", "Cancer of the Larynx", "laryngeal throat cancer", "carcinoma of the larynx", "Laryngeal Throat Cancer", "Carcinoma of the Larynx", "Carcinoma of larynx (disorder)", "carcinoma of larynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laryngeal carcinoma", "shortest_name_length": 13}
{"curie": "MONDO:0001857", "names": ["brucella canis", "Brucella canis", "canine brucellosis", "Canine brucellosis", "canis; brucellosis", "brucellosis; canis", "Canine abortion syndrome", "Brucella canis infection", "Brucella canis brucellosis", "Brucella; infection, canis", "infection; Brucella, canis", "infection due to Brucella canis", "Infection due to Brucella canis", "Brucellosis due to Brucella canis", "Infection caused by Brucella canis", "infection due to Brucella canis (diagnosis)", "Infection caused by Brucella canis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brucella canis brucellosis", "shortest_name_length": 14}
{"curie": "MONDO:0013475", "names": ["CMH18", "hypertrophic cardiomyopathy 18", "PLN hypertrophic cardiomyopathy", "cardiomyopathy, hypertrophic, 18", "hypertrophic cardiomyopathy type 18", "cardiomyopathy familial hypertrophic 18", "CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 18", "cardiomyopathy, familial hypertrophic, 18", "cardiomyopathy, familial hypertrophic, type 18", "hypertrophic cardiomyopathy caused by mutation in PLN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophic cardiomyopathy 18", "shortest_name_length": 5}
{"curie": "MONDO:0100080", "names": ["cardioectodermal syndrome", "cardio-ectodermal syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardioectodermal syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0028618", "names": ["gastroenteric neuroendocrine neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastroenteric neuroendocrine neoplasm", "shortest_name_length": 37}
{"curie": "MONDO:0100402", "names": ["AML, del(13q14-q21)", "AML, del(13)(q14q21)", "AML, del(13)(q14-q21)", "AML, 13q14-q21 Deletion", "AML, del(13q)(13q14-21)", "acute myeloid leukemia, del(13q14-q21)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, del(13q14-q21)", "shortest_name_length": 19}
{"curie": "MONDO:0008060", "names": ["NDNC1", "NDNC10", "growth nail", "NAIL GROWTH", "nail growth", "nail Growth", "trachonychia", "Trachonychia", "trachyonychia", "Growth of nails", "sandpaper nails", "growth of nails", "NDNC10, FORMERLY", "CLAW-SHAPED NAILS", "claw-Shaped nails", "Twenty-Nail Dystrophy", "twenty-nail dystrophy", "Twenty nail dystrophy", "TWENTY-NAIL DYSTROPHY", "twenty nail dystrophy", "onychodystrophy totalis", "idiopathic trachyonychia", "Growth of nails, function", "Twenty nail dystrophy (disorder)", "ONYCHODYSTROPHY TOTALIS, ISOLATED", "autosomal dominant nail dysplasia", "twenty nail dystrophy (diagnosis)", "onychodystrophy totalis, isolated", "Onychodystrophy Totalis, Isolated", "autosomal recessive nail dysplasia", "FZD6 inherited isolated nail anomaly", "ONYCHAUXIS, HYPONYCHIA, AND ONYCHOLYSIS", "nonsyndromic congenital nail disorder 1", "onychauxis, hyponychia, and onycholysis", "nail disorder, nonsyndromic congenital 1", "nonsyndromic congenital nail disorder 10", "NAIL DISORDER, NONSYNDROMIC CONGENITAL, 1", "nail disorder, nonsyndromic congenital, 1", "nail disorder, nonsyndromic congenital, 10", "nonsyndromic congenital nail disorder type 1", "nonsyndromic congenital nail disorder type 10", "Growth of nails, function (observable entity)", "nail disorder, nonsyndromic congenital, type 10", "NAIL DISORDER, NONSYNDROMIC CONGENITAL, 10, FORMERLY", "inherited isolated nail anomaly caused by mutation in FZD6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nonsyndromic congenital nail disorder 1", "shortest_name_length": 5}
{"curie": "UMLS:C5670676", "names": ["Stage IIA Cervical Cancer FIGO 2009", "Stage IIA Cervical Carcinoma FIGO 2009"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Cervical Cancer FIGO 2009", "shortest_name_length": 35}
{"curie": "UMLS:C0750951", "names": ["Lenticulostriate Disorder", "Lenticulostriate Disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lenticulostriate Disorders", "shortest_name_length": 25}
{"curie": "MONDO:0006581", "names": ["Sudamina", "sudamina", "Heat Rash", "Heat rash", "heat rash", "HEAT RASH", "Rash;heat", "Rash;sweat", "heat; rash", "rash; heat", "Sweat rash", "sweat rash", "prickly heat", "Prickly heat", "Prickly Heat", "Sweat pimples", "Heat, Prickly", "Miliaria rubra", "MILIARIA RUBRA", "Miliaria Rubra", "miliaria rubra", "rubra; miliaria", "miliaria; rubra", "Miliaria tropicalis", "miliaria crystallina", "miliaria; tropicalis", "tropicalis; miliaria", "Miliaria crystallina", "heat rash (diagnosis)", "crystallina; miliaria", "Miliaria, crystalline", "miliaria; crystallina", "prickly heat - miliaria", "Prickly heat (disorder)", "Miliaria crystallina (disorder)", "miliaria crystallina (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "miliaria rubra", "shortest_name_length": 8}
{"curie": "MONDO:0003524", "names": ["gastric gastrinoma", "Gastric Gastrinoma", "Gastric Gastrin-Producing NET", "gastric gastrin-producing NET", "Gastric Gastrin Producing Tumor", "gastric gastrin producing tumor", "Gastrin Producing Tumor of the Stomach", "gastric G-cell gastrin producing tumor", "gastrin producing tumor of the stomach", "stomach gastrin-producing neuroendocrine tumor", "gastric gastrin-producing neuroendocrine tumor", "Gastric Gastrin-Producing Neuroendocrine Tumor", "gastrin-producing neuroendocrine tumor of stomach", "Gastrin-Producing Neuroendocrine Tumor of the Stomach", "Gastrin Producing Neuroendocrine Tumor of the Stomach", "gastrin producing neuroendocrine tumor of the stomach", "gastrin-producing neuroendocrine tumor of the stomach"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric gastrin-producing neuroendocrine tumor", "shortest_name_length": 18}
{"curie": "MONDO:0014032", "names": ["BDA1C", "brachydactyly type A1C", "brachydactyly, type A1, C", "BRACHYDACTYLY, TYPE A1, C", "GDF5 brachydactyly type A1", "brachydactyly type A1 caused by mutation in GDF5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly type A1C", "shortest_name_length": 5}
{"curie": "UMLS:C0271121", "names": ["Iris Implantation Cyst", "implantation; cyst, iris", "cyst; implantation, iris", "Implantation cyst of iris", "Primary Iris Stromal Cyst", "Implantation Cyst of Iris", "Implantation Cyst of the Iris", "Acquired Epithelial Implantation Cyst of the Iris"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Iris Implantation Cyst", "shortest_name_length": 22}
{"curie": "UMLS:C4054388", "names": ["Nephrotic Syndrome - EMP2 Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - EMP2 Associated", "shortest_name_length": 36}
{"curie": "MONDO:0007697", "names": ["HAND CLASPING PATTERN", "hand clasping pattern"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hand clasping pattern", "shortest_name_length": 21}
{"curie": "UMLS:C0564755", "names": ["Appendicitis perforated", "Acute Perforated Appendicitis", "Acute perforated appendicitis", "acute perforated appendicitis", "Acute perforated appendicitis (disorder)", "acute perforated appendicitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute perforated appendicitis", "shortest_name_length": 23}
{"curie": "MONDO:0035875", "names": ["ivermectin toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ivermectin toxicity", "shortest_name_length": 19}
{"curie": "MONDO:0008576", "names": ["toe, fifth, number of phalanges 1N", "toe, fifth, number of phalanges IN", "TOE, FIFTH, NUMBER OF PHALANGES IN", "toe, fifth, number of phalanges type 1N"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "toe, fifth, number of phalanges 1N", "shortest_name_length": 34}
{"curie": "MONDO:0005264", "names": ["TIA", "tia", "tias", "T.I.A.", "tia brain", "brain tia", "Brain TIA", "TIA, Brain", "Mini stroke", "Mini-stroke", "Mini-Stroke", "STROKE, TEMPORARY", "transient; attack", "attack; transient", "Transient Ischemic Attack", "attack ischemic transient", "ischemic attack transient", "Transient ischemic attack", "TRANSIENT ISCHEMIC ATTACK", "transient ischemic attack", "TRANSIENT ISCHEMIC ATTACKS", "Transient Ischemic Attacks", "Attack, Transient Ischemic", "Ischemic Attack, Transient", "transient ischemic attacks", "transient ischaemic attack", "ischemic attack, transient", "attacks ischemic transient", "attack, transient ischemic", "Transient ischaemic attack", "TRANSIENT ISCHAEMIC ATTACK", "Transient ischemic attacks", "transient ischaemic attacks", "Attacks, Transient Ischemic", "Transient Cerebral Ischemia", "Transient cerebral ischemia", "Ischemic Attacks, Transient", "Transient ischaemic attacks", "transient cerebral ischemia", "Transient cerebral ischaemia", "Transient Cerebral Ischemias", "Ischemia, Transient Cerebral", "transient cerebral ischaemia", "Cerebral Ischemia, Transient", "CEREBRAL ISCHEMIA, TRANSIENT", "ischemia; cerebral, transient", "cerebral; ischemic, transient", "Ischemias, Transient Cerebral", "Cerebral Ischemias, Transient", "CEREBRAL ISCHEMIA, TRANSITORY", "Ischemia, transient, cerebral", "intermittent cerebral ischemia", "TIA - Transient ischemic attack", "Transient cerebral ischemia NOS", "transient ischemic attack (TIA)", "Transient ischemic attack - TIA", "TIA (Transient Ischemic Attack)", "Transient ischemic attacks (TIA)", "TIA - transient ischaemic attack", "TIA - Transient ischaemic attack", "Transient cerebral ischemia, NOS", "TIAs (Transient Ischemic Attack)", "Transient ischemic attacks (TIAs)", "Transient cerebral ischaemia, NOS", "transient cerebral ischemic attack", "transient ischemic attack (disease)", "Transient ischemic attack (disorder)", "transient ischemic attack (diagnosis)", "Temporary cerebral vascular dysfunction", "Unspecified transient cerebral ischemia", "Temporary cerebral dysfunction, vascular", "Unspecified transient cerebral ischaemia", "Transient cerebral ischemic attack, unspecified", "Transient cerebral ischaemic attack, unspecified", "transient cerebral ischemia (disorder) [ambiguous]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transient ischemic attack", "shortest_name_length": 3}
{"curie": "MONDO:0009594", "names": ["Metaphyseal chondrodysplasia Kaitila type", "metaphyseal chondrodysplasia, Kaitila type", "METAPHYSEAL CHONDRODYSPLASIA, KAITILA TYPE", "Metaphyseal chondrodysplasia, Kaitila type", "Metaphyseal Chondrodysplasia, Kaitila Type", "Metaphyseal chondrodysplasia Kaitila type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metaphyseal chondrodysplasia, Kaitila type", "shortest_name_length": 41}
{"curie": "MONDO:0013007", "names": ["IMD9", "immunodeficiency 9", "IMMUNODEFICIENCY 9", "immunodeficiency type 9", "CID due to ORAI1 deficiency", "Combined immunodeficiency due to ORAI1 deficiency", "combined immunodeficiency due to ORAI1 deficiency", "immune dysfunction with T-cell inactivation due to calcium entry defect 1", "Immune dysfunction with T-cell inactivation due to calcium entry defect 1", "IMMUNE DYSFUNCTION WITH T-CELL INACTIVATION DUE TO CALCIUM ENTRY DEFECT 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined immunodeficiency due to ORAI1 deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0001399", "names": ["Ureter Leiomyoma", "ureter leiomyoma", "Ureteral Leiomyoma", "ureteral leiomyoma", "leiomyoma of ureter", "Leiomyoma of Ureter", "Leiomyoma of the Ureter", "leiomyoma of the ureter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ureter leiomyoma", "shortest_name_length": 16}
{"curie": "MONDO:0018783", "names": ["fibroblastic rheumatism", "Fibroblastic rheumatism", "Fibroblastic rheumatism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibroblastic rheumatism", "shortest_name_length": 23}
{"curie": "UMLS:C1335943", "names": ["Senile Sebaceous Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Senile Sebaceous Hyperplasia", "shortest_name_length": 28}
{"curie": "UMLS:C4682637", "names": ["Stage II Primary Peritoneal Cancer", "Stage II Primary Peritoneal Cancer AJCC v8", "Stage II Primary Peritoneal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Primary Peritoneal Cancer AJCC v8", "shortest_name_length": 34}
{"curie": "UMLS:C4520899", "names": ["stage IV anal cancer", "Stage IV Anal Canal Cancer", "Stage IV Anal Canal Cancer AJCC v6", "Stage IV Anal Canal Cancer AJCC v7", "Stage IV Anal Carcinoma AJCC v6 and v7", "Stage IV Anal Canal Cancer AJCC v6 and v7", "Stage IV Anal Canal Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Anal Canal Cancer AJCC v6 and v7", "shortest_name_length": 20}
{"curie": "MONDO:0008307", "names": ["Kraepelin disease", "catatonia of Kraepelin", "Catatonia of Kraepelin", "PRESENILE DEMENTIA, KRAEPELIN TYPE", "presenile dementia, Kraepelin type", "Presenile dementia, Kraepelin type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "presenile dementia, Kraepelin type", "shortest_name_length": 17}
{"curie": "MONDO:0004932", "names": ["null-cell leukemia", "null-cell leukaemia", "Null cell acute lymphoblastic leukemia", "null cell acute lymphoblastic leukemia", "Null cell acute lymphoblastic leukaemia", "Null cell acute lymphoblastic leukemia (disorder)", "Null cell acute lymphoblastic leukemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "null-cell leukemia", "shortest_name_length": 18}
{"curie": "UMLS:C1336302", "names": ["Stage II Nodular Lymphocyte Predominant Hodgkin Lymphoma", "Stage II Nodular Lymphocyte Predominant Hodgkin's Disease", "Stage II Nodular Lymphocyte Predominant Hodgkin's Lymphoma", "Stage II Hodgkin's Disease Nodular Lymphocyte Predominance Type", "Stage II Hodgkin's Lymphoma Nodular Lymphocyte Predominance Type", "Ann Arbor Stage II Nodular Lymphocyte Predominant Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage II Nodular Lymphocyte Predominant Hodgkin Lymphoma", "shortest_name_length": 56}
{"curie": "MONDO:0013953", "names": ["IMD28", "Ifngr2 deficiency", "IFNGR2 Deficiency", "IFNGR2 DEFICIENCY", "IFNGR2 deficiency", "IFNGR 2 Deficiency", "immunodeficiency 28", "IMMUNODEFICIENCY 28", "immunodeficiency type 28", "immunodeficiency 28, mycobacteriosis", "immunodeficiency 28, Mycobacteriosis", "Interferon Gamma Receptor 2 Deficiency", "IFNGR2 primary immunodeficiency disease", "MSMD due to complete IFNgammaR2 deficiency", "IMMUNODEFICIENCY 28, MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE", "MSMD due to complete interferon gamma receptor 2 deficiency", "primary immunodeficiency disease caused by mutation in IFNGR2", "Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency", "Mendelian susceptibility to mycobacterial diseases due to complete interferon gamma receptor 2 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 28", "shortest_name_length": 5}
{"curie": "MONDO:0001656", "names": ["Achalasia", "achalasia", "ACHALASIA", "Achalasias", "Cardiospasm", "cardiospasm", "CARDIOSPASM", "Cardiospasms", "cardiospasms", "Megaesophagus", "megaesophagus", "Megaoesophagus", "achalasia cardia", "Cardiospasm, NOS", "Achalasia Cardia", "Esophagus dilated", "ACHALASIA CARDIAE", "Achalasia cardiae", "Achalasia of cardia", "Achalasia of Cardia", "achalasia esophagus", "esophagus achalasia", "esophageal achalasia", "Achalasia esophageal", "ACHALASIA ESOPHAGEAL", "Esophageal Achalasia", "Esophageal achalasia", "oesophageal achalasia", "achalasia cardiospasm", "Esophageal Achalasias", "Achalasia, Esophageal", "achalasia (diagnosis)", "Achalasia oesophageal", "Achalasia;oesophageal", "Oesophageal achalasia", "achalasia of esophagus", "Esophagus achalasia of", "Achalasia of esophagus", "Achalasias, Esophageal", "Oesophagus achalasia of", "Achalasia of oesophagus", "Megaesophagus (disorder)", "megaesophagus (diagnosis)", "Achalasia and cardiospasm", "Achalasia of the esophagus", "Achalasia of the oesophagus", "Achalasia of esophagus (disorder)", "Hypertensive lower esophageal sphincter", "Hypertensive lower oesophageal sphincter", "Lower esophageal sphincter, lack of reflex relaxation", "Lack of reflex relaxation of lower esophageal sphincter", "Lack of reflex relaxation of lower oesophageal sphincter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "megaesophagus", "shortest_name_length": 9}
{"curie": "MONDO:0017527", "names": ["preaxial polydactyly type 3, unilateral", "polydactyly of an index finger, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polydactyly of an index finger, unilateral", "shortest_name_length": 39}
{"curie": "MONDO:0002783", "names": ["Shwartzman Reaction", "Shwartzman reaction", "Schwartzman Reaction", "SCHWARTZMAN REACTION", "Schwartzman Reactions", "Shwartzman Phenomenon", "Shwartzman phenomenon", "Phenomenon, Shwartzman", "Schwartzman Phenomenon", "Phenomenon, Schwartzman", "Shwartzman reaction, NOS", "Shwartzman reaction, function", "Shwartzman reaction (function)", "Shwartzman reaction, function (observable entity)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Shwartzman phenomenon", "shortest_name_length": 19}
{"curie": "MONDO:0003253", "names": ["Vulvar Granular Cell Tumor", "vulvar granular cell tumor", "mammalian vulva granular cell tumor", "granular cell tumor of mammalian vulva"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar granular cell tumor", "shortest_name_length": 26}
{"curie": "MONDO:0018534", "names": ["squamous cell carcinoma of liver and IBT", "squamous cell carcinoma of liver and intrahepatic biliary tract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "squamous cell carcinoma of liver and intrahepatic biliary tract", "shortest_name_length": 40}
{"curie": "MONDO:0010964", "names": ["EDM3", "multiple epiphyseal dysplasia 3", "Multiple epiphyseal dysplasia 3", "epiphyseal dysplasia multiple 3", "Epiphyseal dysplasia, multiple, 3", "epiphyseal dysplasia, multiple, 3", "EPIPHYSEAL DYSPLASIA, MULTIPLE, 3", "epiphyseal dysplasia, multiple, type 3", "COL9A3 multiple epiphyseal dysplasia (disease)", "EPIPHYSEAL DYSPLASIA, MULTIPLE, 3, WITH MYOPATHY", "epiphyseal dysplasia, multiple, 3, with myopathy", "multiple epiphyseal dysplasia 3 with or without myopathy", "epiphyseal dysplasia, multiple, 3, with or without myopathy", "multiple epiphyseal dysplasia (disease) caused by mutation in COL9A3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epiphyseal dysplasia, multiple, 3", "shortest_name_length": 4}
{"curie": "MONDO:0008873", "names": ["MOPD3", "Mopd 3", "MOPD III", "Mopd, Sicilian fairy type", "MOPD, SICILIAN FAIRY TYPE", "Mopd, Caroline Crachami type", "MOPD, CAROLINE CRACHAMI TYPE", "osteodysplastic primordial dwarfism, type 3", "Osteodysplastic primordial dwarfism, type 3", "OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III", "Osteodysplastic Primordial Dwarfism, Type III", "microcephalic osteodysplastic primordial dwarfism, type 3", "Microcephalic osteodysplastic primordial dwarfism, type 3", "MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III", "Microcephalic Osteodysplastic Primordial Dwarfism, Type III", "microcephalic osteodysplastic primordial dwarfism, type III", "MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, SICILIAN FAIRY TYPE", "microcephalic osteodysplastic primordial dwarfism, Sicilian fairy type", "Microcephalic osteodysplastic primordial dwarfism, Sicilian fairy type", "MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, CAROLINE CRACHAMI TYPE", "microcephalic osteodysplastic primordial dwarfism, Caroline Crachami type", "Microcephalic osteodysplastic primordial dwarfism, Caroline Crachami type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephalic osteodysplastic primordial dwarfism, type 3", "shortest_name_length": 5}
{"curie": "MONDO:0011246", "names": ["MDCMC", "congenital megaconial myopathy", "Congenital megaconial myopathy", "megaconial congénital muscular dystrophy", "Megaconial congenital muscular dystrophy", "megaconial congenital muscular dystrophy", "megaconial type congenital muscular dystrophy", "muscular dystrophy, congenital, megaconial type", "MUSCULAR DYSTROPHY, CONGENITAL, MEGACONIAL TYPE", "Muscular Dystrophy, Congenital, Megaconial Type", "Megaconial congenital muscular dystrophy (disorder)", "congenital muscular dystrophy with mitochondrial structural abnormalities", "Congenital muscular dystrophy with mitochondrial structural abnormalities", "muscular dystrophy, congenital, with mitochondrial structural abnormalities", "MUSCULAR DYSTROPHY, CONGENITAL, WITH MITOCHONDRIAL STRUCTURAL ABNORMALITIES", "Congenital muscular dystrophy due to phosphatidylcholine biosynthesis defect", "congenital muscular dystrophy due to phosphatidylcholine biosynthesis defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "megaconial type congenital muscular dystrophy", "shortest_name_length": 5}
{"curie": "MONDO:0025130", "names": ["SVD", "Swine vesicular disease", "swine vesicular disease", "Swine Vesicular Disease", "swine vesicular diseases", "Vesicular Disease, Swine", "Swine Vesicular Diseases", "vesicular disease, swine", "vesicular diseases, swine", "Vesicular Diseases, Swine", "vesicular disease of pigs", "swine vesicular disease (SVD)", "Swine vesicular disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "swine vesicular disease", "shortest_name_length": 3}
{"curie": "MONDO:0006460", "names": ["Thyroglossal Cyst", "thyroglossal cyst", "Cyst;thyroglossal", "Thyrolingual Cyst", "Thyroglossal cyst", "thyrolingual cyst", "Thyrolingual Cysts", "Thyroglossal Cysts", "cysts thyroglossal", "thyroglossal cysts", "cyst; thyroglossal", "thyroglossal; cyst", "Cyst, Thyroglossal", "Cyst, Thyrolingual", "Cysts, Thyrolingual", "Cysts, Thyroglossal", "Thyroglossal duct/cyst", "thyroglossal duct cyst", "Thyroglossal Duct Cyst", "THYROGLOSSAL DUCT CYST", "cyst duct thyroglossal", "Thyroglossal duct cyst", "cyst; thyroglossal duct", "Thyroglossal duct/cyst/", "THYROGLOSSAL DUCT, CYST", "Cyst, Thyroglossal Duct", "thyroglossal duct cysts", "thyroglossal tract cyst", "Thyroglossal Duct Cysts", "Cysts, Thyroglossal Duct", "Congenital thyroglossal cyst", "thyroglossal cyst (diagnosis)", "Thyroglossal duct cyst (disorder)", "Congenital thyroglossal duct cyst"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroglossal duct cyst", "shortest_name_length": 17}
{"curie": "MONDO:0000338", "names": ["variola major", "Variola major", "Variola major (disorder)", "variola major (diagnosis)", "variola major infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "variola major infectious disease", "shortest_name_length": 13}
{"curie": "UMLS:C0155860", "names": ["Pseudomonas pneumonia", "Pseudomonal pneumonia", "Pneumonia pseudomonal", "Pseudomonas; pneumonia", "pneumonia; Pseudomonas", "Pneumonitis pseudomonas", "Pneumonia due to Pseudomonas", "Pneumonia due to pseudomonas", "pneumonia due to Pseudomonas", "PNEUMONIA BACTERIAL PSEUDOMONAS", "Pneumonia caused by Pseudomonas", "pneumonia due to Pseudomonas (diagnosis)", "Pneumonia caused by Pseudomonas (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pneumonia due to Pseudomonas", "shortest_name_length": 21}
{"curie": "MONDO:0017335", "names": ["tetrasomy 11q24.1", "microtriplication 11q24.1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microtriplication 11q24.1", "shortest_name_length": 17}
{"curie": "UMLS:C0233652", "names": ["Palinopsia", "palinopsia", "Visual perseveration", "Palinopsia (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "palinopsia", "shortest_name_length": 10}
{"curie": "MONDO:0016117", "names": ["Muscular lipidosis", "muscular lipidosis", "Lipid storage myopathy", "Lipid Storage Myopathy", "lipid storage myopathy", "Lipid storage myopathy (disorder)", "Myopathy with Abnormal Lipid Metabolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular lipidosis", "shortest_name_length": 18}
{"curie": "MONDO:0013382", "names": ["THMD4", "Progressive polyneuropathy with bilateral striatal necrosis", "progressive polyneuropathy with bilateral striatal necrosis", "STRIATAL NECROSIS, BILATERAL, AND PROGRESSIVE POLYNEUROPATHY", "striatal Necrosis, bilateral, and progressive polyneuropathy", "bilateral striatal Degeneration and progressive polyneuropathy", "BILATERAL STRIATAL DEGENERATION AND PROGRESSIVE POLYNEUROPATHY", "progressive demyelinating neuropathy with bilateral striatal necrosis", "Progressive polyneuropathy with bilateral striatal necrosis (disorder)", "thiamine metabolism dysfunction syndrome 4 (progressive polyneuropathy type)", "thiamine metabolism dysfunction syndrome 4 (bilateral striatal degeneration and progressive polyneuropathy type)", "THIAMINE METABOLISM DYSFUNCTION SYNDROME 4 (BILATERAL STRIATAL DEGENERATION AND PROGRESSIVE POLYNEUROPATHY TYPE)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive demyelinating neuropathy with bilateral striatal necrosis", "shortest_name_length": 5}
{"curie": "MONDO:0023200", "names": ["Fryns Fabry Remans syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fryns Fabry Remans syndrome", "shortest_name_length": 27}
{"curie": "MONDO:0016466", "names": ["asbestosis", "ASBESTOSIS", "Asbestoses", "Asbestosis", "asbestoses", "Amianthosis", "Pulmonary asbestosis", "PULMONARY ASBESTOSIS", "pulmonary asbestosis", "Asbestosis (disorder)", "Asbestos intoxication", "asbestos intoxication", "asbestos intoxination", "asbestosis (diagnosis)", "Asbestos pneumoconiosis", "asbestos pneumoconiosis", "asbestos dust pneumoconiosis", "pneumoconiosis from asbestos dust", "pulmonary fibrosis - from asbestos exposure", "idiopathic interstitial pneumonitis - from asbestos exposure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "asbestosis", "shortest_name_length": 10}
{"curie": "UMLS:C2984087", "names": ["Colorectal Cancer by AJCC v7 Stage", "Colorectal Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Cancer by AJCC v7 Stage", "shortest_name_length": 34}
{"curie": "MONDO:0017291", "names": ["RCVS", "reversible cerebral vasoconstriction syndrome", "Reversible cerebral vasoconstriction syndrome", "Reversible cerebral vasoconstriction syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "reversible cerebral vasoconstriction syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0278820", "names": ["Bladder Cancer Stage 0", "stage 0 bladder cancer", "Stage 0 Bladder Cancer", "bladder cancer, stage 0", "Stage 0 Bladder Carcinoma", "Stage 0 Carcinoma of Bladder", "stage 0 cancer of the bladder", "Stage 0 Bladder Cancer AJCC v6", "cancer of the bladder, stage 0", "Stage 0 Bladder Cancer AJCC v7", "stage 0 carcinoma of the bladder", "Stage 0 Carcinoma of the Bladder", "stage 0 bladder carcinoma in situ", "Stage 0 Urinary Bladder Carcinoma", "carcinoma of the bladder, stage 0", "Stage 0 Carcinoma of Urinary Bladder", "Stage 0 Bladder Cancer AJCC v6 and v7", "Stage 0 Carcinoma of the Urinary Bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Bladder Carcinoma", "shortest_name_length": 22}
{"curie": "MONDO:0012384", "names": ["Pand3", "PAND3", "panic disorder 3", "PANIC DISORDER 3", "panic disorder type 3", "PANIC DISORDER SUSCEPTIBILITY LOCUS, CHROMOSOME 4q-RELATED", "panic disorder susceptibility locus, chromosome 4Q-related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "panic disorder 3", "shortest_name_length": 5}
{"curie": "UMLS:C5556701", "names": ["Refractory Acute Myeloid Leukemia with Myelodysplasia-Related Changes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Acute Myeloid Leukemia with Myelodysplasia-Related Changes", "shortest_name_length": 69}
{"curie": "UMLS:C4053823", "names": ["mTOR Inhibitor - Induced Nephropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mTOR Inhibitor - Induced Nephropathy", "shortest_name_length": 36}
{"curie": "MONDO:0002610", "names": ["purpura", "PURPURA", "Purpura", "Purpuras", "peliosis", "PURPURAS", "Peliosis", "purpuras", "Purpura NOS", "Blood spots", "Purpura, NOS", "SKIN PURPURA", "skin purpura", "purpura skin", "Peliosis, NOS", "Purpura of skin", "purpura was seen", "Purpuric disorder", "purpura (disease)", "purpuric disorder", "Purpura (disorder)", "purpura (diagnosis)", "purpura (physical finding)", "Purpuric disorder (disorder)", "Red or purple spots on the skin", "Disorder characterised by purpura", "Purpura (morphologic abnormality)", "Disorder characterized by purpura"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "purpura", "shortest_name_length": 7}
{"curie": "UMLS:C4553243", "names": ["Stage II Thyroid Gland Follicular Cancer", "Stage II Thyroid Gland Follicular Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Thyroid Gland Follicular Carcinoma AJCC v8", "shortest_name_length": 40}
{"curie": "MONDO:0019314", "names": ["solitary mastocytoma", "multiple mastocytoma", "cutaneous mastocytoma", "cutaneous local mastocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous mastocytoma", "shortest_name_length": 20}
{"curie": "MONDO:0020491", "names": ["BH", "SBH", "HeCo", "SCLH", "DC SYNDROME", "Double cortex", "BAND HETEROTOPIA", "band heterotopia", "Band heterotopia", "Band heterotopias", "heterotopic cortex", "DOUBLE CORTEX SYNDROME", "double cortex syndrome", "Double cortex syndrome", "Double Cortex Syndrome", "Syndrome, Double Cortex", "familial band heterotopia", "subcortical band heterotopia", "Subcortical band heterotopia", "Subcortical Band Heterotopia", "SUBCORTICAL BAND HETEROTOPIA", "Heterotopia, Subcortical Band", "Subcortical Band Heterotopias", "Heterotopias, Subcortical Band", "subcortical laminar heterotopia", "SUBCORTICAL LAMINAR HETEROTOPIA", "Subcortical laminar heterotopia", "Subcortical Laminar Heterotopia", "Heterotopia, Subcortical Laminar", "Heterotopias, Subcortical Laminar"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subcortical band heterotopia", "shortest_name_length": 2}
{"curie": "MONDO:0700078", "names": ["Triple Positive", "Triple-Positive", "Triple positive breast cancer", "triple positive breast cancer", "Hormone Receptor/HER2 Positive", "triple-positive breast carcinoma", "Triple-Positive Breast Cancer Finding", "HR-positive HER2 positive breast cancer", "hormone receptor positive her2 positive breast cancer", "Hormone Receptor/Epidermal Growth Factor Receptor 2 Positive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "triple-positive breast carcinoma", "shortest_name_length": 15}
{"curie": "MONDO:0002244", "names": ["F7 deficiency", "F7 DEFICIENCY", "SPCA DEFICIENCY", "deficiency; SPCA", "SPCA; deficiency", "Deficiency, stable", "deficiency, stable", "factor 7 deficiency", "Factor 7 deficiency", "Factor 7 Deficiency", "HYPOPROCONVERTINEMIA", "Deficiency, Factor 7", "Hypoproconvertinemia", "FACTOR VII DEFICIENCY", "Factor VII deficiency", "factor vii deficiency", "Hypoproconvertinemias", "Factor VII Deficiency", "Factor 7 Deficiencies", "factor VII deficiency", "Deficiencies, Factor 7", "Deficiency, factor VII", "Deficiency, Factor VII", "Factor VII Deficiencies", "Factor Seven Deficiency", "PROCONVERTIN DEFICIENCY", "Deficiencies, Factor VII", "STABLE FACTOR DEFICIENCY", "Stable factor deficiency", "Deficiency, Factor Seven", "proconvertin; deficiency", "deficiency; proconvertin", "Factor Seven Deficiencies", "deficiency; stable factor", "stable factor; deficiency", "Factor VII deficiency, NOS", "Deficiencies, Factor Seven", "F7 - Factor VII deficiency", "Deficiency of stable factor", "Reduced factor VII activity", "Stable factor deficiency, NOS", "disorder deficiency vii factor", "Factor VII deficiency (disorder)", "congenital factor VII deficiency", "Congenital factor VII deficiency", "deficiency; proconvertin, acquired", "Congenital proconvertin deficiency", "proconvertin; deficiency, acquired", "congenital factor VII deficiency (diagnosis)", "Prothrombin conversion accelerator deficiency", "SERUM PROTHROMBIN CONVERSION ACCELERATOR DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "factor VII deficiency", "shortest_name_length": 13}
{"curie": "MONDO:0009440", "names": ["KIDAR", "Desmons syndrome", "DESMONS SYNDROME", "Kid Syndrome, Autosomal Recessive", "KID SYNDROME, AUTOSOMAL RECESSIVE", "KID syndrome, autosomal recessive", "ichthyosiform erythroderma, corneal involvement, deafness", "Ichthyosiform erythroderma, corneal involvement, deafness", "Autosomal recessive keratitis-ichthyosis-deafness syndrome", "Keratitis-ichthyosis-deafness syndrome, autosomal recessive", "keratitis-ichthyosis-deafness syndrome, autosomal recessive", "KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL RECESSIVE", "ICHTHYOSIFORM ERYTHRODERMA, CORNEAL INVOLVEMENT, AND DEAFNESS", "ichthyosiform erythroderma, corneal involvement, and deafness", "Ichthyosiform Erythroderma, Corneal Involvement, And Deafness", "ichthyosiform erythroderma-corneal involvement-deafness syndrome", "ichthyosiform erythroderma, corneal involvement, and hearing loss", "Autosomal recessive KID (keratitis, ichthyosis, deafness) syndrome", "Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ichthyosiform erythroderma, corneal involvement, and hearing loss", "shortest_name_length": 5}
{"curie": "UMLS:C1335105", "names": ["Old Burn Scar-Related Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Old Burn Scar-Related Neoplasm", "shortest_name_length": 30}
{"curie": "MONDO:0009107", "names": ["DD", "DTD", "Diastrophic dwarf", "Dwarf, diastrophic", "diastrophic dwarfism", "Diastrophic dwarfism", "diastrophic dysplasia", "Diastrophic dysplasia", "DIASTROPHIC DYSPLASIA", "Diastrophic Dysplasia", "DD - Diastrophic dysplasia", "DTD - Diastrophic dysplasia", "Diastrophic nanism syndrome", "Diastrophic dwarfism syndrome", "Diastrophic dysplasia syndrome", "Diastrophic dysplasia (disorder)", "diastrophic dysplasia (diagnosis)", "diastrophic dysplasia, Broad bone-Platyspondylic variant", "DIASTROPHIC DYSPLASIA, BROAD BONE-PLATYSPONDYLIC VARIANT", "Diastrophic Dysplasia, Broad Bone-Platyspondylic Variant", "osteochondrodysplasia with defects of growth of tubular bones and spine diastrophic dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diastrophic dysplasia", "shortest_name_length": 2}
{"curie": "UMLS:C2362324", "names": ["Child Obesity", "Obesity, Child", "Childhood obesity", "childhood obesity", "Pediatric Obesity", "Childhood Obesity", "Obesity, Pediatric", "Obesity, Childhood", "Obesity in children", "Obesity in Children", "Obesity in Childhood", "Obesity in childhood", "Childhood Onset Obesity", "Obesity, Childhood Onset", "Obesity, childhood onset", "Obesity, childhood-onset", "Childhood obesity (disorder)", "childhood obesity (diagnosis)", "Childhood obesity BMI 95-100 percentile"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pediatric Obesity", "shortest_name_length": 13}
{"curie": "MONDO:0016434", "names": ["acquired dermis elastic tissue disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired dermis elastic tissue disorder", "shortest_name_length": 39}
{"curie": "MONDO:0014224", "names": ["MRT38", "mental retardation, autosomal recessive 38", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 38", "mental retardation, autosomal recessive type 38", "intellectual disability, autosomal recessive 38", "developmental delay with ASD and gait instability", "intellectual disability, autosomal recessive type 38", "autosomal recessive intellectual developmental disorder 38", "intellectual developmental disorder, autosomal recessive 38", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 38", "developmental delay with autism spectrum disorder and gait instability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental delay with autism spectrum disorder and gait instability", "shortest_name_length": 5}
{"curie": "UMLS:C1263855", "names": ["LUMBAR RADICULOPATHY", "radiculopathy lumbar", "Lumbar radiculopathy", "lumbar radiculopathy", "Lumbar radiculopathy, NOS", "Radiculopathy, lumbar region", "Lumbar radiculopathy (disorder)", "lumbar radiculopathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lumbar radiculopathy", "shortest_name_length": 20}
{"curie": "MONDO:0023833", "names": ["multifocal choroiditis", "Multifocal choroiditis", "choroiditis multifocal", "Multifocal Choroiditis", "Choroiditis, Multifocal", "MFC-multifocal choroiditis", "Multifocal choroiditis (disorder)", "Multifocal choroiditis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multifocal choroiditis", "shortest_name_length": 22}
{"curie": "UMLS:C1699654", "names": ["Esophageal Mucositis", "Esophageal mucositis", "Oesophageal mucositis", "mucositis of esophagus", "mucositis of esophagus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal mucositis", "shortest_name_length": 20}
{"curie": "MONDO:0010423", "names": ["HYSP2", "Hysp2", "Hypospadias 2, X-Linked", "hypospadias 2, X-linked", "HYPOSPADIAS 2, X-LINKED", "hypospadias 2, X-linked, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypospadias 2, X-linked", "shortest_name_length": 5}
{"curie": "MONDO:0020492", "names": ["macrencephaly", "hemimegalencephaly", "Hemimegalencephaly", "Hemimegalencephalies", "Unilateral Macrocephaly", "Macrocephaly, Unilateral", "unilateral megalencephaly", "Unilateral Macrocephalies", "Unilateral megalencephaly", "Unilateral Megalencephaly", "Megalencephaly, Unilateral", "Macrocephalies, Unilateral", "Unilateral Megalencephalies", "Megalencephalies, Unilateral", "Hemimegalencephaly (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemimegalencephaly", "shortest_name_length": 13}
{"curie": "MONDO:0005465", "names": ["methamphetamine-induced psychosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "methamphetamine-induced psychosis", "shortest_name_length": 33}
{"curie": "MONDO:0030736", "names": ["ODG10", "ovarian dysgenesis 10", "OVARIAN DYSGENESIS 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian dysgenesis 10", "shortest_name_length": 5}
{"curie": "MONDO:0019031", "names": ["XDAT", "congenital dyserythropoietic anemia with thombocytopenia", "Congenital dyserythropoietic anemia with thombocytopenia", "Thrombocytopenia with congenital dyserythropoietic anemia", "thrombocytopenia with congenital dyserythropoietic anemia", "X-linked congenital dyserythropoietic anemia with thrombocytopenia", "X-linked congenital dyserythropoietic anaemia with thrombocytopenia", "X-linked congenital dyserythropoietic anemia with thrombocytopenia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombocytopenia with congenital dyserythropoietic anemia", "shortest_name_length": 4}
{"curie": "MONDO:0008145", "names": ["Ollier", "Ecchondrosis", "ecchondrosis", "Ollier Disease", "ollier disease", "OLLIER DISEASE", "Ollier disease", "Kast's syndrome", "olliers disease", "Disease, Ollier", "Olliers Disease", "DYSCHONDROPLASIA", "Enchondromatosis", "dyschondroplasia", "Enchondromatoses", "Dyschondroplasia", "ollier's disease", "Ollier's disease", "enchondromatosis", "Ollier's Disease", "Dyschondroplasias", "Disease, Ollier's", "Osteochondromatoses", "OSTEOCHONDROMATOSIS", "osteochondromatosis", "Osteochondromatosis", "multiple enchondroma", "Multiple Enchondroma", "Bessel-Hagen disease", "Multiple Enchondrosis", "Enchondroma, Multiple", "Multiple Enchondroses", "multiple enchondromas", "Multiple Enchondromas", "Enchondrosis, Multiple", "Enchondroses, Multiple", "Enchondromas, Multiple", "Multiple enchondromata", "Osteochondromatosis NOS", "Multiple Osteochondromas", "Osteochondromatosis, NOS", "Multiple osteochondromas", "enchondromatosis multiple", "Multiple enchondromatosis", "Enchondromatosis syndrome", "multiple enchondromatosis", "Enchondromatosis, Multiple", "CHONDROMATOSIS, UNILATERAL", "ENCHONDROMATOSIS, MULTIPLE", "enchondromatosis, multiple", "Congenital enchondromatosis", "Enchondromatosis (disorder)", "Ollier type enchondromatosis", "Enchondromatosis, congenital", "dyschondroplasia (diagnosis)", "Multiple cartilaginous exostoses", "enchondromatosis with haemangiomata", "Enchondromatosis with haemangiomata", "multiple cartilaginous enchondroses", "ENCHONDROSES, MULTIPLE, CARTILAGINOUS", "enchondromatosis, multiple, Ollier type", "ENCHONDROMATOSIS, MULTIPLE, OLLIER TYPE", "Osteochondromatosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ollier disease", "shortest_name_length": 6}
{"curie": "MONDO:0014828", "names": ["ICF3", "ICF syndrome 3", "immunodeficiency-centromeric instability-Facial anomalies syndrome 3", "IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 3", "immunodeficiency-centromeric instability-FACIAL anomalies syndrome 3", "immunodeficiency-centromeric instability-facial anomalies syndrome 3", "CDCA7 immunodeficiency-centromeric instability-facial anomalies syndrome", "immunodeficiency-centromeric instability-facial anomalies syndrome type 3", "immunodeficiency-centromeric instability-Facial anomalies syndrome type 3", "immunodeficiency-centromeric instability-facial anomalies syndrome caused by mutation in CDCA7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency-centromeric instability-facial anomalies syndrome 3", "shortest_name_length": 4}
{"curie": "UMLS:C4683237", "names": ["Pathologic Stage I Retinoblastoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage I Retinoblastoma AJCC v8", "shortest_name_length": 41}
{"curie": "MONDO:0029134", "names": ["IMD58", "immunodeficiency 58", "IMMUNODEFICIENCY 58", "severe combined immunodeficiency due to CARMIL2 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe combined immunodeficiency due to CARMIL2 deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C1698666", "names": ["Lip Infection", "Lip infection", "infection of lip", "Infection of lip", "Infection of lip (disorder)", "infection of lip (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lip Infection", "shortest_name_length": 13}
{"curie": "MONDO:0008769", "names": ["CLN2", "CLN2 disease", "Jansky-Bielschowsky disease", "CLN2 disease, juvenile (subtype)", "neuronal ceroid lipofuscinosis 2", "CEROID LIPOFUSCINOSIS, NEURONAL, 2", "ceroid lipofuscinosis, neuronal, 2", "Ceroid Lipofuscinosis, Neuronal, 2", "TPP1 neuronal ceroid lipofuscinosis", "Neuronal Ceroid Lipofuscinosis Type 2", "neuronal ceroid lipofuscinosis type 2", "CLN2 disease, late infantile (subtype)", "ceroid lipofuscinosis, neuronal, type 2", "late infantile neuronal ceroid lipofuscinosis", "Late Infantile Neuronal Ceroid Lipofuscinosis", "neuronal ceroid lipofuscinosis, late infantile", "neuronal ceroid lipofuscinosis 2 variable age at onset", "neuronal ceroid lipofuscinosis caused by mutation in TPP1", "CEROID LIPOFUSCINOSIS, NEURONAL, 2, VARIABLE AGE AT ONSET", "ceroid lipofuscinosis, neuronal, 2, variable Age at onset", "Ceroid Lipofuscinosis, Neuronal, 2, Variable Age At Onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuronal ceroid lipofuscinosis 2", "shortest_name_length": 4}
{"curie": "MONDO:0014065", "names": ["MC3DN4", "UQCRQ mitochondrial complex III deficiency", "mitochondrial Complex 3 deficiency, nuclear type 4", "mitochondrial complex III deficiency nuclear type 4", "mitochondrial complex III deficiency, nuclear type 4", "MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 4", "mitochondrial complex III deficiency caused by mutation in UQCRQ"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex III deficiency nuclear type 4", "shortest_name_length": 6}
{"curie": "UMLS:C0149952", "names": ["Torsed ovary", "torsed ovary", "ovary torsion", "torsion ovary", "torsion; ovary", "OVARY, TORSION", "ovary; torsion", "Ovarian Torsion", "OVARIAN TORSION", "Ovarian torsion", "ovarian torsion", "Ovarian Torsions", "Torsion of ovary", "torsion of ovary", "Torsion, Ovarian", "Torsions, Ovarian", "Torsion of ovary (disorder)", "ovarian torsion (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Torsion", "shortest_name_length": 12}
{"curie": "MONDO:0009894", "names": ["SRTD6", "SRPS2A", "Srps, type 2", "SRPS, TYPE II", "MAJEWSKI SYNDROME", "Majewski Syndrome", "Majewski syndrome", "Short-rib syndrome, type II", "Short rib-polydactyly syndrome type 2", "short rib-polydactyly syndrome, type 2", "Short Rib-Polydactyly Syndrome Type II", "short rib-polydactyly syndrome type II", "Type II short rib polydactyly syndrome", "Short Rib Polydactyly Syndrome, Type II", "short rib-polydactyly syndrome, type 2A", "SHORT RIB-POLYDACTYLY SYNDROME, TYPE II", "short rib-polydactyly syndrome type IIA", "Short Rib-Polydactyly Syndrome, Type II", "SHORT RIB-POLYDACTYLY SYNDROME, TYPE IIA", "Majewski-type short rib polydactyly syndrome", "Short Rib-Polydactyly Syndrome, Majewski Type", "Short Rib Polydactyly Syndrome, Majewski Type", "Short rib-polydactyly syndrome, Majewski type", "polydactyly with neonatal chondrodystrophy type II", "polydactyly with neonatal chondrodystrophy, type 2", "Polydactyly with Neonatal Chondrodystrophy, Type 2", "Polydactyly with Neonatal Chondrodystrophy Type II", "Polydactyly With Neonatal Chondrodystrophy, Type II", "polydactyly with neonatal chondrodystrophy, type II", "POLYDACTYLY WITH NEONATAL CHONDRODYSTROPHY, TYPE II", "Short rib-polydactyly syndrome, Majewski type (disorder)", "Short-Rib Thoracic Dysplasia 6 with or without Polydactyly", "short-rib thoracic dysplasia 6 with or without polydactyly", "SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short-rib thoracic dysplasia 6 with or without polydactyly", "shortest_name_length": 5}
{"curie": "UMLS:C4527171", "names": ["Stage IV Cutaneous (Skin) Melanoma", "Clinical Stage IV Cutaneous Melanoma AJCC v8", "Clinical Stage IV Melanoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage IV Cutaneous Melanoma AJCC v8", "shortest_name_length": 34}
{"curie": "UMLS:C1096248", "names": ["Alternaria infection", "Alternaria; infection", "infection; Alternaria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alternaria infection", "shortest_name_length": 20}
{"curie": "UMLS:C1710167", "names": ["Sporadic Thyroid Gland Micromedullary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sporadic Thyroid Gland Micromedullary Carcinoma", "shortest_name_length": 47}
{"curie": "MONDO:0025294", "names": ["Tick Borne Disease", "tick borne disease", "borne disease tick", "Tick-Borne Disease", "Tick-borne disease", "tick-borne disease", "Disease, Tick Borne", "disease, Tick-borne", "tick borne diseases", "diseases tick-borne", "Tick-Borne Diseases", "Tick Borne Diseases", "Tick borne diseases", "Disease, Tick-Borne", "Borne Disease, Tick", "Tick-borne diseases", "tick-borne diseases", "Diseases, Tick Borne", "Diseases, Tick-Borne", "diseases, Tick-borne", "Tick-borne infection", "Borne Diseases, Tick", "infection, Tick-borne", "Tick borne infections", "Tick-borne infections", "infections, Tick-borne", "infections, Tick borne", "Disease transmitted by tick", "tick-borne infectious disease", "Tick-borne infectious disease", "Disease transmitted by tick (navigational concept)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tick-borne infectious disease", "shortest_name_length": 18}
{"curie": "UMLS:C1882970", "names": ["Salivary Gland Adenocarcinoma, NOS", "Salivary Gland Adenocarcinoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Salivary Gland Adenocarcinoma, Not Otherwise Specified", "shortest_name_length": 34}
{"curie": "UMLS:C0038045", "names": ["SPRAIN", "sprain", "Sprain", "Sprains", "SPRAINS", "sprain nos", "Sprain, NOS", "sprain (diagnosis)", "Sprain (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sprain", "shortest_name_length": 6}
{"curie": "MONDO:0002118", "names": ["uropathy", "UROPATHY", "Uropathy", "urinary disease", "Urologic Disease", "Urologic disease", "urologic disease", "disease urologic", "Urologic Disorder", "urologic disorder", "disease, urologic", "Urologic Diseases", "Disease, Urologic", "diseases urologic", "urologic diseases", "disease urological", "Urological Disease", "Diseases, Urologic", "Disease;urological", "urological disease", "urologic disorders", "diseases, urologic", "urological disorder", "Disease, Urological", "Urological disorder", "Urological Diseases", "urological diseases", "disease, urological", "disorder urological", "urological disorders", "Urological Disorders", "diseases, urological", "disorders urological", "Diseases, Urological", "renal system disease", "Urinary Tract Disease", "urinary tract disease", "disease tract urinary", "Urologic disease, NOS", "DISORDER URINARY TRACT", "urinary system disease", "disease system urinary", "urinary tract disorder", "diseases tract urinary", "URINARY TRACT DISORDER", "Urinary Tract Diseases", "Urinary system disease", "urinary tract diseases", "disorder urinary tract", "Disorder urinary tract", "disease urinary system", "Urinary tract disorder", "Urinary Tract Disorder", "disease, urinary tract", "Disease, Urinary Tract", "urinary tract disorders", "disorders tract urinary", "urinary renal disorders", "Diseases, Urinary Tract", "diseases system urinary", "renal urinary disorders", "Urinary Tract Disorders", "Urinary system disorder", "urinary system diseases", "Urinary System Disorder", "diseases, urinary tract", "disease of renal system", "urinary system disorder", "disorder of renal system", "disorders system urinary", "URINARY SYSTEM DISORDERS", "diseases systems urinary", "urinary system disorders", "Urinary tract disorder of", "URINARY TRACT DISORDER OF", "Disorder of urinary tract", "Syndrome of urinary tract", "disorder of urinary system", "Urinary tract disorder NOS", "Disorder of Urinary System", "disorders of urinary tract", "renal and urinary disorders", "Renal and urinary disorders", "Disease of urinary tract, NOS", "Syndrome of urinary tract, NOS", "Disorder of the urinary system", "disorder of the urinary system", "diseases of the urinary system", "Disorder of urinary tract, NOS", "Diseases of the urinary system", "urologic disorders (diagnosis)", "Disorder of urinary tract proper", "renal system disease or disorder", "disease or disorder of renal system", "non-neoplastic urinary tract disease", "disease (or disorder); urinary tract", "Disease or syndrome of urinary tract", "Non-Neoplastic Urinary Tract Disease", "Non-neoplastic urinary tract disease", "Non-Neoplastic Urinary Tract Disorder", "kidney/urinary disease (non-specific)", "Non-Neoplastic Urinary System Disorder", "disorders of urinary tract (diagnosis)", "Disorder of urinary system, unspecified", "renal and urinary disorders (diagnosis)", "Diseases and Syndromes of Urinary Tract", "Disorder of the urinary system (disorder)", "Disorder of urinary tract proper (disorder)", "DISEASES AND SYNDROMES OF THE URINARY TRACT", "Unspecified disorder of urethra and urinary tract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urinary system disorder", "shortest_name_length": 8}
{"curie": "MONDO:0003225", "names": ["myelopathy", "Bone Marrow Disease", "Bone marrow disease", "bone marrow disease", "Disease, Bone Marrow", "Bone marrow disorder", "Bone Marrow Diseases", "bone marrow; disease", "bone marrow diseases", "Marrow Disease, Bone", "bone marrow disorder", "Bone Marrow Disorder", "Bone marrow--Diseases", "Diseases, Bone Marrow", "Marrow Diseases, Bone", "disease of bone marrow", "disorder of bone marrow", "Bone marrow disorder NOS", "Bone marrow disorder (disorder)", "bone marrow disease or disorder", "Anomaly of the bone marrow cells", "disease or disorder of bone marrow", "disease (or disorder); bone marrow", "Abnormality of bone marrow cell morphology"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bone marrow disorder", "shortest_name_length": 10}
{"curie": "MONDO:0010732", "names": ["Wells-Jankovic syndrome", "Wells Jankovic Syndrome", "Wells Jankovic syndrome", "spastic paraparesis - deafness", "spastic paraparesis and deafness", "SPASTIC PARAPARESIS AND DEAFNESS", "Spastic Paraparesis and Deafness", "Spastic paraparesis and deafness", "spastic paraplegia with deafness", "Spastic paraparesis with deafness", "paraparesis spastic with deafness", "Spastic paraparesis-deafness syndrome", "spastic paraparesis-deafness syndrome", "Familial spastic paraparesis and deafness", "familial spastic paraparesis and deafness", "Spastic paraparesis-hearing loss syndrome", "Spastic paraparesis with deafness (diagnosis)", "Spastic paraparesis co-occurrent with deafness", "Spastic paraparesis co-occurrent with deafness (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic paraparesis-deafness syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0100322", "names": ["non-Zellweger spectrum disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-Zellweger spectrum disorder", "shortest_name_length": 31}
{"curie": "UMLS:C5236091", "names": ["Sinonasal Exophytic Papilloma", "Sinonasal Exophytic Schneiderian Papilloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Exophytic Papilloma", "shortest_name_length": 29}
{"curie": "OMIM:203760", "names": ["MEIGEL DISEASE", "Meigel Disease", "ALPHA-2-DEFICIENT COLLAGEN DISEASE", "Alpha-2-Deficient Collagen Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 14}
{"curie": "MONDO:0002131", "names": ["jaw cancer", "jaw neoplasm", "Jaw Neoplasms", "neoplasm of jaw", "jaw skeleton cancer", "cancer of jaw skeleton", "malignant jaw skeleton neoplasm", "malignant neoplasm of jaw skeleton"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "jaw cancer", "shortest_name_length": 10}
{"curie": "UMLS:C5420047", "names": ["Sinonasal Rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Rhabdomyosarcoma", "shortest_name_length": 26}
{"curie": "MONDO:0012147", "names": ["Chds5", "CHDS5", "KALRN coronary artery disease", "Early-onset coronary artery disease", "coronary artery disease, early-onset", "CORONARY ARTERY DISEASE, EARLY-ONSET", "Coronary artery disease, early-onset", "susceptibility to coronary heart disease 5", "coronary heart disease, susceptibility to, 5", "CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 5", "coronary heart disease, susceptibility to, type 5", "coronary artery disease caused by mutation in KALRN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coronary heart disease, susceptibility to, 5", "shortest_name_length": 5}
{"curie": "UMLS:C5238928", "names": ["Gastrointestinal Tract Acute Graft Versus Host Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal Tract Acute Graft Versus Host Disease", "shortest_name_length": 54}
{"curie": "MONDO:0010780", "names": ["MMIT", "benign COX deficiency", "mitochondrial myopathy, infantile, transient", "MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT", "Cox deficiency myopathy, infantile, transient", "COX DEFICIENCY MYOPATHY, INFANTILE, TRANSIENT", "reversible infantile respiratory chain deficiency", "RESPIRATORY CHAIN DEFICIENCY, INFANTILE, TRANSIENT", "respiratory chain deficiency, infantile, transient", "reversible infantile cytochrome C oxidase deficiency", "mitochondrial myopathy with reversible COX deficiency", "mitochondrial myopathy with reversible complex IV deficiency", "infantile reversible cytochrome C oxidase deficiency myopathy", "mitochondrial myopathy with reversible cytochrome C oxidase deficiency", "MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT, DUE TO RESPIRATORY CHAIN DEFICIENCY", "mitochondrial myopathy, infantile, transient, due to respiratory chain deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial myopathy with reversible cytochrome C oxidase deficiency", "shortest_name_length": 4}
{"curie": "UMLS:C4288010", "names": ["Vulvar Fibroadenoma", "Vulvar Ectopic Fibroadenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Fibroadenoma", "shortest_name_length": 19}
{"curie": "UMLS:C2936445", "names": ["Septic Sacroiliitis", "Sacroiliitis, Septic", "Septic Sacroiliitides", "Sacroiliitides, Septic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Septic Sacroiliitis", "shortest_name_length": 19}
{"curie": "MONDO:0037743", "names": ["mediastinal soft tissue cancer", "malignant mediastinal mesenchymal tumor", "Malignant Mediastinal Soft Tissue Tumor", "malignant mediastinal soft tissue tumor", "mediastinal mesenchymal tumor, malignant", "malignant soft tissue tumor of mediastinum", "Malignant Mediastinal Soft Tissue Neoplasm", "malignant mediastinal soft tissue neoplasm", "Malignant Soft Tissue Tumor of Mediastinum", "Malignant Soft Tissue Neoplasm of Mediastinum", "malignant soft tissue neoplasm of mediastinum", "Malignant Soft Tissue Tumor of the Mediastinum", "malignant soft tissue tumor of the mediastinum", "Malignant Soft Tissue Neoplasm of the Mediastinum", "malignant soft tissue neoplasm of the mediastinum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mediastinal soft tissue cancer", "shortest_name_length": 30}
{"curie": "UMLS:C1868890", "names": ["Pseudocholelithiasis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pseudocholelithiasis", "shortest_name_length": 20}
{"curie": "MONDO:0019603", "names": ["osteopenia-myopia-hearing loss-intellectual disability-facial dysmorphism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteopenia-myopia-hearing loss-intellectual disability-facial dysmorphism syndrome", "shortest_name_length": 82}
{"curie": "MONDO:0010662", "names": ["Fitzsimmons syndrome", "Fitzsimmons McLachlan Gilbert syndrome", "Fitzsimmons-McLachlan-Gilbert syndrome", "Paraplegia-intellectual disability-hyperkeratosis syndrome", "paraplegia-intellectual disability-hyperkeratosis syndrome", "mental retardation with spastic paraplegia and palmoplantar hyperkeratosis", "mental retardation-spastic paraplegia-palmoplantar hyperkeratosis syndrome", "Mental retardation with spastic paraplegia and palmoplantar hyperkeratosis", "MENTAL RETARDATION WITH SPASTIC PARAPLEGIA AND PALMOPLANTAR HYPERKERATOSIS", "intellectual disability with spastic paraplegia and palmoplantar hyperkeratosis", "Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome", "Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome (disorder)", "Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paraplegia-intellectual disability-hyperkeratosis syndrome", "shortest_name_length": 20}
{"curie": "MONDO:0032648", "names": ["MCCCHCM", "MEGA-CORPUS-CALLOSUM SYNDROME WITH CEREBELLAR HYPOPLASIA AND CORTICAL MALFORMATIONS", "mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations", "shortest_name_length": 7}
{"curie": "MONDO:0019431", "names": ["primitive portal vein thrombosis", "non-cirrhotic portal vein thrombosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primitive portal vein thrombosis", "shortest_name_length": 32}
{"curie": "UMLS:C1516064", "names": ["Astler-Coller B2 Rectal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Astler-Coller B2 Rectal Carcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C1698678", "names": ["gastrointestinal stoma necrosis", "Gastrointestinal stoma necrosis", "Gastrointestinal Stoma Necrotic Lesion", "gastrointestinal stoma necrosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal Stoma Necrotic Lesion", "shortest_name_length": 31}
{"curie": "MONDO:0020760", "names": ["Bowen's disease of skin", "Intraepidermal carcinoma of skin", "skin squamous cell cancer in situ", "Skin Squamous Cell Cancer In Situ", "Cancer in situ skin, squamous cell", "Skin Squamous Cell Carcinoma In Situ", "skin squamous cell carcinoma in situ", "Intraepidermal Squamous Cell Carcinoma", "intraepidermal squamous cell carcinoma", "Intraepidermal squamous cell carcinoma", "IEC - Intraepidermal carcinoma of skin", "Squamous Cell Carcinoma in situ of Skin", "Squamous cell carcinoma of skin in situ", "squamous cell carcinoma in situ of skin", "Squamous cell carcinoma in situ of skin", "squamous cell carcinoma in situ of the skin", "Squamous Cell Carcinoma in situ of the Skin", "SCC - Squamous cell carcinoma in situ of skin", "Squamous cell carcinoma in situ of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin squamous cell carcinoma in situ", "shortest_name_length": 23}
{"curie": "UMLS:C4745162", "names": ["Resectable Extrahepatic Bile Duct Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Extrahepatic Bile Duct Adenocarcinoma", "shortest_name_length": 48}
{"curie": "UMLS:C4527057", "names": ["Clinical Stage 0 Merkel Cell Carcinoma AJCC v8", "Clinical Stage 0 Neuroendocrine Carcinoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage 0 Merkel Cell Carcinoma AJCC v8", "shortest_name_length": 46}
{"curie": "UMLS:C0151664", "names": ["gi perforation", "GI perforation", "GI PERFORATION", "Perforation gastrointestinal", "gastrointestinal perforation", "Gastrointestinal perforation", "PERFORATION GASTROINTESTINAL", "Digestive System Perforation", "Gastrointestinal Perforation", "Gastrointestinal perforation NOS", "Gastrointestinal perforation, NOS", "GASTROINTESTINAL PERFORATION (NOS)", "Gastrointestinal perforation (NOS)", "Gastrointestinal perforation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal perforation", "shortest_name_length": 14}
{"curie": "UMLS:C3890429", "names": ["Liquid Tumor", "Blood Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liquid Tumor", "shortest_name_length": 12}
{"curie": "UMLS:C5237970", "names": ["Pancreatobiliary Cancer", "Pancreaticobiliary Cancer", "Pancreatobiliary Carcinoma", "Pancreaticobiliary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatobiliary Carcinoma", "shortest_name_length": 23}
{"curie": "MONDO:0005193", "names": ["pin", "PIN", "Prostate intraepithelial neopl.", "prostate intraepithelial neopl.", "Prostatic Intraepithelial Neoplasm", "prostate intraepithelial neoplasia", "Prostatic Intraepithelial Neoplasia", "Intraepithelial Neoplasm, Prostatic", "Intraepithelial Prostatic Neoplasia", "Prostatic Intraepithelial Neoplasms", "Prostatic intraepithelial neoplasia", "prostatic intraepithelial neoplasia", "Neoplasm, Prostatic Intraepithelial", "Intraepithelial Neoplasms, Prostatic", "Intraepithelial Neoplasia, Prostatic", "Prostatic Neoplasia, Intraepithelial", "Neoplasia, Prostatic Intraepithelial", "Intraepithelial Prostatic Neoplasias", "Neoplasia, Intraepithelial Prostatic", "Prostatic Intraepithelial Neoplasias", "Neoplasms, Prostatic Intraepithelial", "Prostate intraepithelial neoplasia (PIN)", "prostate gland intraepithelial neoplasia", "prostate intraepithelial neoplasia (pin)", "PIN - Prostatic Intraepithelial Neoplasia", "pin - prostatic intraepithelial neoplasia", "PIN - Prostatic intraepithelial neoplasia", "Prostatic intraepithelial neoplasia (disorder)", "Prostatic intraepithelial neoplasia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate intraepithelial neoplasia", "shortest_name_length": 3}
{"curie": "UMLS:C0751510", "names": ["Sleep Related Neurogenic Tachypnea", "Sleep-related neurogenic tachypnea", "Sleep-Related Neurogenic Tachypnea", "Tachypnea, Sleep-Related Neurogenic", "Neurogenic Tachypnea, Sleep-Related", "Sleep-Related Neurogenic Tachypneas", "Sleep-related neurogenic tachypnoea", "Neurogenic Tachypneas, Sleep-Related", "Tachypneas, Sleep-Related Neurogenic", "Sleep-related neurogenic tachypnea (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sleep-Related Neurogenic Tachypnea", "shortest_name_length": 34}
{"curie": "UMLS:C4720862", "names": ["Metastatic non-small cell carcinoma", "Metastatic Non-Small Cell Carcinoma", "Metastatic non-small cell carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic non-small cell carcinoma", "shortest_name_length": 35}
{"curie": "MONDO:0100248", "names": ["rapidly progressive PCNSV", "rapidly progressive primary central nervous system vasculitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rapidly progressive primary central nervous system vasculitis", "shortest_name_length": 25}
{"curie": "MONDO:0015766", "names": ["CHOLERA", "cholera", "Cholera", "choleras", "Choleras", "Cholera, NOS", "ASIATIC CHOLERA", "Vibrio cholerae", "asiatic cholera", "epidemic cholera", "EPIDEMIC CHOLERA", "Classical cholera", "Cholera (disorder)", "classical; cholera", "cholera; classical", "cholera (diagnosis)", "Unspecified cholera", "Cholera, unspecified", "VIBRIO CHOLERA INFECTION", "cholera - Vibrio cholerae", "Vibrio cholerae Infection", "Vibrio cholerae infection", "Cholera - Vibrio cholerae", "Vibrio cholerae Infections", "Infection, Vibrio cholerae", "Infections, Vibrio cholerae", "Vibrio cholerae 01; cholera", "cholera due to Vibrio cholerae", "Cholera due to Vibrio cholerae", "Cholera due to vibrio cholerae", "Vibrio cholera gastroenteritis", "Vibrio cholerae gastroenteritis", "Cholera - O1 group Vibrio cholerae", "Vibrio cholerae infectious disease", "Vibrio cholerae disease or disorder", "cholera due to Vibrio cholerae (diagnosis)", "Vibrio cholerae caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholera", "shortest_name_length": 7}
{"curie": "UMLS:C3697021", "names": ["NOH", "Nodular Oncocytic Hyperplasia", "Nodular oncocytic hyperplasia", "Multifocal nodular hyperplasia of salivary gland", "Multifocal nodular oncocytic hyperplasia of salivary gland", "Multifocal nodular oncocytic hyperplasia of salivary gland (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Multifocal nodular oncocytic hyperplasia of salivary gland", "shortest_name_length": 3}
{"curie": "MONDO:0002917", "names": ["Hair Disease", "HAIR DISEASE", "hair disease", "hair diseases", "diseases hair", "hair disorder", "Hair Problems", "DISORDER HAIR", "disorder hair", "Hair Diseases", "Hair Disorder", "disease hairs", "Disorder hair", "Hair disorder", "HAIR DISORDER", "disorders hair", "Hair Disorders", "hair disorders", "Hair--Diseases", "DISEASE OF HAIR", "Disorder of hair", "Hair disorder NOS", "HAIR DISORDER NOS", "disorders follicle hair", "diseases of hair follicles", "pilosebaceous unit disease", "Disorder of hair (disorder)", "hair/hair follicle diseases", "disease of pilosebaceous unit", "disorder of pilosebaceous unit", "hair and hair follicle disease", "hair and hair follicle disorder", "Hair and hair follicle diseases", "hair and hair follicle diseases", "disease of hair and hair follicles", "Diseases of hair and hair follicles", "pilosebaceous unit disease or disorder", "Disease of hair and hair follicle, NOS", "DISEASES OF THE HAIR AND HAIR FOLLICLES", "disease or disorder of pilosebaceous unit", "Unspecified disease of hair and hair follicles", "disease of hair and hair follicles (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of pilosebaceous unit", "shortest_name_length": 12}
{"curie": "MONDO:0017353", "names": ["neonatal NKH", "classic glycine encephalopathy", "neonatal glycine encephalopathy", "neonatal non-ketotic hyperglycinemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal glycine encephalopathy", "shortest_name_length": 12}
{"curie": "MONDO:0013906", "names": ["AI2A4", "ODAPH amelogenesis imperfecta", "amelogenesis imperfecta type IIA4", "amelogenesis imperfecta, type IIA4", "amelogenesis imperfecta hypomaturation type 2A4", "amelogenesis imperfecta hypomaturation type IIA4", "AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA4", "amelogenesis imperfecta, hypomaturation type, IIA4", "amelogenesis imperfecta caused by mutation in ODAPH"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amelogenesis imperfecta hypomaturation type 2A4", "shortest_name_length": 5}
{"curie": "MONDO:0000249", "names": ["secretory diarrhea", "Secretory diarrhea", "Secretory diarrhoea", "Diarrhea, secretory", "secretory diarrhoea", "Secretory diarrhea (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secretory diarrhea", "shortest_name_length": 18}
{"curie": "UMLS:C1696085", "names": ["Visceral edema", "Visceral Edema", "Visceral oedema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Visceral edema", "shortest_name_length": 14}
{"curie": "MONDO:0008714", "names": ["acrofacial dysostosis Rodriguez type", "Acrofacial dysostosis Rodriguez type", "acrofacial dysostosis, Rodríguez type", "Acrofacial dysostosis, Rodríguez type", "ACROFACIAL DYSOSTOSIS SYNDROME OF RODRIGUEZ", "Acrofacial Dysostosis Syndrome Of Rodriguez", "acrofacial dysostosis syndrome of Rodriguez", "acrofacial dysostosis, syndrome of Rodriguez", "RODRIGUEZ LETHAL ACROFACIAL DYSOSTOSIS SYNDROME", "Acrofacial dysostosis Rodriguez type (disorder)", "Rodriguez lethal acrofacial dysostosis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acrofacial dysostosis Rodriguez type", "shortest_name_length": 36}
{"curie": "UMLS:C3641709", "names": ["ENSAT Stage I Adrenal Cortex Cancer", "ENSAT Stage I Adrenal Cortex Carcinoma", "ENSAT Stage I Adrenal Cortical Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ENSAT Stage I Adrenal Cortical Carcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C1334606", "names": ["Malignant Neoplasm by Grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Neoplasm by Grade", "shortest_name_length": 27}
{"curie": "MONDO:0003935", "names": ["Oncocytic Breast Carcinoma", "oncocytic breast carcinoma", "Breast Oncocytic Carcinoma", "breast oncocytic carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oncocytic breast carcinoma", "shortest_name_length": 26}
{"curie": "UMLS:C0752258", "names": ["Position Sense Disorder", "Position Sense Disorders", "Sense Disorder, Position", "Sense Disorders, Position"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Position Sense Disorders", "shortest_name_length": 23}
{"curie": "UMLS:C2987128", "names": ["Gastrointestinal NEC", "Gastrointestinal NEC G3", "Gastrointestinal Neuroendocrine Carcinoma", "Digestive System Neuroendocrine Carcinoma", "Gastrointestinal neuroendocrine carcinoma", "Gastrointestinal System Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal neuroendocrine carcinoma", "shortest_name_length": 20}
{"curie": "MONDO:0006865", "names": ["ANUG", "anug", "mouth trench", "Trench mouth", "Trench Mouth", "trench mouth", "angina vincent", "VINCENT ANGINA", "Vincent Angina", "Plaut's angina", "Vincent angina", "vincent angina", "vincents angina", "Fusospirillosis", "fusospirillosis", "Vincent disease", "Vincents angina", "VINCENT'S ANGINA", "Vincent's Angina", "vincent's angina", "Vincent's angina", "Vincent Infection", "Angina - Vincents", "angina; vincent's", "angina - Vincents", "Vincent's disease", "Fusospirochetosis", "Vincent's infection", "vincent's infection", "Vincent's Infection", "Vincent's Stomatitis", "vincent's gingivitis", "infection; vincent's", "Vincent's gingivitis", "vincent's; infection", "Vincent's Gingivitis", "Plaut-Vincent angina", "Vincent's stomatitis", "stomatitis vincent's", "vincent's stomatitis", "phagedenic gingivitis", "Phagedenic Gingivitis", "vincent's; stomatitis", "gingivitis; vincent's", "Spirochetal stomatitis", "necrotizing gingivitis", "Necrotising gingivitis", "NECROTIZING GINGIVITIS", "Necrotizing gingivitis", "Spirochaetal stomatitis", "spirochetal; stomatitis", "stomatitis; spirochetal", "Fusospirillary gingivitis", "Fusospirillary Gingivitis", "Fusospirochetal pharyngitis", "acute membranous gingivitis", "Acute Membranous Gingivitis", "Acute ulcerative gingivitis", "Acute necrotizing gingivitis", "ulcerative gingivostomatitis", "Fusospirochaetal pharyngitis", "acute necrotizing gingivitis", "Vincent angina - pharyngitis", "Vincent's angina (diagnosis)", "Ulcerative Gingivostomatitis", "Vincent's infection, any site", "Vincent's angina - pharyngitis", "gingivitis; acute, necrotizing", "acute; gingivitis, necrotizing", "Vincent's infection (diagnosis)", "Vincent's gingivitis (diagnosis)", "acute ulceromembranous gingivitis", "necrotizing ulcerative gingivitis", "Necrotizing Ulcerative Gingivitis", "AUG - Acute ulcerative gingivitis", "Necrotizing ulcerative gingivitis", "Necrotising ulcerative gingivitis", "Acute ulceromembranous gingivitis", "gingivitis necrotizing ulcerative", "Gingivitis, Necrotizing ulcerative", "early acute necrotising gingivitis", "gingivitis; necrotizing ulcerative", "Gingivitis, Necrotizing Ulcerative", "necrotizing ulcerative; gingivitis", "Acute ulcerative gingivitis (disorder)", "Acute necrotizing ulcerative stomatitis", "Acute Necrotizing Ulcerative Gingivitis", "acute necrotising ulcerative gingivitis", "Acute necrotizing ulcerative gingivitis", "acute necrotizing ulcerative gingivitis", "Acute necrotising ulcerative gingivitis", "Vincent's angina - pharyngitis (disorder)", "Necrotizing ulcerative (acute) gingivitis", "Necrotizing ulcerative gingivitis (disorder)", "necrotizing ulcerative gingivitis (diagnosis)", "ANUG - acute necrotising ulcerative gingivitis", "acute necrotizing ulcerative gingivostomatitis", "Acute necrotizing ulcerative gingivostomatitis", "Acute necrotising ulcerative gingivostomatitis", "ANUG - Acute necrotizing ulcerative gingivitis", "ANUG - Acute necrotising ulcerative gingivitis", "acute necrotising ulcerative gingivostomatitis", "ANUG - acute necrotizing ulcerative gingivitis", "Necrotizing ulcerative (acute) gingivostomatitis", "Acute necrotizing ulcerative gingivitis (disorder)", "acute necrotising ulcerative gingivitis [ambiguous]", "acute necrotizing ulcerative gingivitis (diagnosis)", "Acute necrotizing ulcerative gingivostomatitis (disorder)", "acute necrotising ulcerative gingivostomatitis [ambiguous]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "necrotizing ulcerative gingivitis", "shortest_name_length": 4}
{"curie": "UMLS:C5238560", "names": ["High Risk Plasma Cell Myeloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Risk Plasma Cell Myeloma", "shortest_name_length": 29}
{"curie": "MONDO:0030798", "names": ["IMD99", "IMMUNODEFICIENCY 99 WITH HYPOGAMMAGLOBULINEMIA AND AUTOIMMUNE CYTOPENIAS", "immunodeficiency 99 with hypogammaglobulinemia and autoimmune cytopenias"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 99 with hypogammaglobulinemia and autoimmune cytopenias", "shortest_name_length": 5}
{"curie": "UMLS:C0855138", "names": ["Refractory Mantle Cell Lymphoma", "Mantle Cell Lymphoma Refractory", "Mantle cell lymphoma refractory"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mantle cell lymphoma refractory", "shortest_name_length": 31}
{"curie": "MONDO:0002679", "names": ["Infarct cerebral", "Cerebral infarct", "INFARCT CEREBRAL", "cerebral infarct", "Cerebral Infarct", "infarct cerebral", "CEREBRAL INFARCT", "cerebral infarcts", "cerebral ischemia", "Cerebral Ischemia", "Infarct, Cerebral", "Cerebral Infarcts", "Cerebral infarcts", "Infarcts, Cerebral", "Cerebral Infarction", "CEREBRAL INFARCTION", "cerebral infarction", "Cerebral infarction", "infarction cerebral", "Infarction;cerebral", "Infarction, Cerebral", "infarction, cerebral", "infarction; cerebral", "cerebral; infarction", "cerebral infarctions", "cerebral, infarction", "Cerebral Infarctions", "Infarctions, Cerebral", "Cerebral infarction, NOS", "CI - Cerebral infarction", "CVA - cerebral infarction", "CVA - Cerebral infarction", "Cerebral vascular infarction", "telencephalon brain infarction", "Cerebral infarction (disorder)", "cerebral infarction (diagnosis)", "Cerebral infarction, unspecified", "brain infarction of telencephalon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral infarction", "shortest_name_length": 16}
{"curie": "MONDO:0032583", "names": ["MCPH24", "microcephaly 24, primary, autosomal recessive", "MICROCEPHALY 24, PRIMARY, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly 24, primary, autosomal recessive", "shortest_name_length": 6}
{"curie": "UMLS:C0264714", "names": ["Acute heart failure", "acute heart failure", "heart failure acute", "acute failure heart", "Heart failure, acute", "acute cardiac failure", "Cardiac failure acute", "sudden; heart failure", "cardiac failure acute", "heart failure; sudden", "Acute cardiac insufficiency", "Acute heart failure (disorder)", "acute cardiac failure (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute heart failure", "shortest_name_length": 19}
{"curie": "UMLS:C1274305", "names": ["Benign Skin Fibrohistiocytic Neoplasm", "Benign fibrohistiocytic neoplasm of skin", "Benign Cutaneous Fibrohistiocytic Neoplasm", "Benign fibrohistiocytic neoplasm of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign fibrohistiocytic neoplasm of skin", "shortest_name_length": 37}
{"curie": "UMLS:C0333882", "names": ["Moderate Glandular Cell Atypia", "Moderate glandular cell atypia", "Moderate glandular cell atypia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Moderate glandular cell atypia", "shortest_name_length": 30}
{"curie": "UMLS:C4745010", "names": ["Benign Peritoneal and Retroperitoneal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Peritoneal and Retroperitoneal Neoplasm", "shortest_name_length": 46}
{"curie": "MONDO:0002452", "names": ["Prostate Leiomyoma", "prostate leiomyoma", "Prostatic leiomyoma", "prostatic leiomyoma", "Prostatic Leiomyoma", "leiomyoma of prostate", "Leiomyoma of Prostate", "prostate gland leiomyoma", "leiomyoma of the prostate", "Leiomyoma of the Prostate", "leiomyoma of prostate gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate leiomyoma", "shortest_name_length": 18}
{"curie": "MONDO:0009941", "names": ["Pygmy", "PYGMY", "Pygmy, African", "PYGMY, AFRICAN", "Pygmy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pygmy", "shortest_name_length": 5}
{"curie": "MONDO:0008392", "names": ["HMSN I", "Roussy-Lévy", "ataxia; Roussy-Lévy", "Roussy-Levy Disease", "Roussy-Lévy; ataxia", "Roussy-levy disease", "Roussy Levy Disease", "Roussy-Levy syndrome", "Roussy-levy syndrome", "roussy-levy syndrome", "Levy-Roussy syndrome", "Roussy-Levy Syndrome", "ROUSSY-LEVY SYNDROME", "Roussy Levy Syndrome", "Roussy Levy syndrome", "levy-roussy syndrome", "Roussy levy syndrome", "Roussy-Lévy syndrome", "Syndrome, Roussy-Levy", "ROUSSY-LEVY POLYNEUROPATHY", "hereditary areflexic dystasia", "Hereditary Areflexic Dystasia", "Hereditary areflexic dystasia", "Dystasia, Hereditary Areflexic", "Areflexic Dystasia, Hereditary", "Hereditary Areflexic Dystasias", "Areflexic Dystasias, Hereditary", "Roussy-Levy Syndrome (disorder)", "Roussy-Lévy syndrome (disorder)", "Dystasias, Hereditary Areflexic", "Roussy-Levy syndrome (diagnosis)", "Charcot-Marie-Tooth disease (variant)", "hereditary motor sensory neuropathy I", "Charcot-Marie-Tooth-Roussy-levy disease", "ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIA", "Roussy levy hereditary areflexic dystasia", "Roussy-Levy Hereditary Areflexic Dystasia", "Roussy-levy hereditary areflexic dystasia", "Roussy Levy Hereditary Areflexic Dystasia", "Hereditary ataxia-muscular atrophy syndrome", "Hereditary areflexic dystasia, Roussy-Lévy type", "hereditary areflexic dystasia, Roussy-levy type", "hereditary areflexic dystasia, Roussy-Lévy type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Roussy-Levy syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C4745161", "names": ["Resectable Digestive System Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Digestive System Carcinoma", "shortest_name_length": 37}
{"curie": "UMLS:C5206772", "names": ["Recurrent Epithelioid Malignant Peripheral Nerve Sheath Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Epithelioid Malignant Peripheral Nerve Sheath Tumor", "shortest_name_length": 61}
{"curie": "MONDO:0023142", "names": ["fetal brain disruption sequence"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fetal brain disruption sequence", "shortest_name_length": 31}
{"curie": "MONDO:0014962", "names": ["MRT57", "mental retardation, autosomal recessive 57", "intellectual disability, autosomal recessive 57", "mental retardation, autosomal recessive type 57", "intellectual disability, autosomal recessive type 57", "autosomal recessive intellectual developmental disorder 57", "intellectual developmental disorder, autosomal recessive 57", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 57", "MBOAT7 autosomal recessive non-syndromic intellectual disability", "autosomal recessive non-syndromic intellectual disability caused by mutation in MBOAT7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 57", "shortest_name_length": 5}
{"curie": "UMLS:C0687707", "names": ["Anorectal Disease", "Anorectal Diseases", "Anorectal Disorder", "Anorectal diseases", "Anorectal disorder", "ANORECTAL DISORDER", "anorectal disorder", "anorectal disorders", "Anorectal Disorders", "Ano-rectal disorder NOS", "Disorder anorectal (NOS)", "DISORDER ANORECTAL (NOS)", "Anorectal disorder (disorder)", "anorectal disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anorectal Diseases", "shortest_name_length": 17}
{"curie": "MONDO:0014660", "names": ["MCPH15", "NEDMISBA", "primary autosomal recessive microcephaly 15", "MICROCEPHALY 15, PRIMARY, AUTOSOMAL RECESSIVE", "microcephaly 15, primary, autosomal recessive", "neurodevelopmental disorder with progressive microcephaly, spasticity, and brain abnormalities", "neurodevelopmental disorder with progressive microcephaly, spasticity, and brain imaging abnormalities", "NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN IMAGING ABNORMALITIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly 15, primary, autosomal recessive", "shortest_name_length": 6}
{"curie": "MONDO:0001135", "names": ["voyeurism", "Voyeurism", "Voyeurisms", "Voyeurism (disorder)", "voyeurism (diagnosis)", "sexual; deviation, voyeurism", "deviation; sexual, voyeurism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "voyeurism", "shortest_name_length": 9}
{"curie": "UMLS:C0855093", "names": ["B Cell Lymphoma Stage III", "Stage III B Cell Lymphoma", "B-cell lymphoma stage III", "Stage III B-Cell Lymphoma", "B-Cell Lymphoma Stage III", "Stage III B-Cell Non-Hodgkin Lymphoma", "Stage III B-Cell Non-Hodgkin's Lymphoma", "Ann Arbor Stage III B-Cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-cell lymphoma stage III", "shortest_name_length": 25}
{"curie": "MONDO:0012425", "names": ["FECD2", "FCD1 LOCUS", "Fcd1 locus", "Fuchs' endothelial corneal dystrophy 2", "corneal dystrophy, fuchs endothelial, 2", "Corneal Dystrophy, Fuchs Endothelial, 2", "corneal dystrophy, Fuchs endothelial, 2", "CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 2", "Corneal dystrophy, Fuchs' endothelial, 2", "Late-onset Fuchs' endothelial corneal dystrophy", "CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, LATE-ONSET", "corneal dystrophy, Fuchs endothelial, late-onset", "Corneal dystrophy, Fuchs' endothelial, late-onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal dystrophy, fuchs endothelial, 2", "shortest_name_length": 5}
{"curie": "MONDO:0017766", "names": ["disorder of manganese transport"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of manganese transport", "shortest_name_length": 31}
{"curie": "MONDO:0002816", "names": ["Cortex", "Adrenal Cortex Disease", "adrenal cortex disease", "Cortex Disease, Adrenal", "adrenal cortex disorder", "Disease, Adrenal Cortex", "Adrenal Cortex Diseases", "Cortex Diseases, Adrenal", "Diseases, Adrenal Cortex", "Adrenal cortex--Diseases", "disease of adrenal cortex", "Disease of adrenal cortex", "adrenal cortical disorder", "disorder of adrenal cortex", "Disorder of adrenal cortex", "adrenal cortex disease or disorder", "Disorder of adrenal cortex (disorder)", "disease or disorder of adrenal cortex"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adrenal cortex disorder", "shortest_name_length": 6}
{"curie": "UMLS:C5555058", "names": ["BCOR-CCNB3 Sarcoma", "BCOR::CCNB3 Sarcoma", "BCOR-Rearranged Sarcoma", "BCOR-CCNB3 Fusion-Positive Sarcoma", "BCOR::CCNB3 Fusion-Positive Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "BCOR-CCNB3 Sarcoma", "shortest_name_length": 18}
{"curie": "UMLS:C0349398", "names": ["Paranoid delusion", "paranoid delusion", "Delusion, paranoid", "paranoid delusions", "Paranoid delusions", "persecutory delusion", "delusion of persecution", "delusions of persecution", "Paranoid delusion (finding)", "paranoid delusions (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paranoid delusion", "shortest_name_length": 17}
{"curie": "UMLS:C4324477", "names": ["Transformation to acute myeloid leukemia", "Transformation to acute myeloid leukaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transformation to acute myeloid leukemia", "shortest_name_length": 40}
{"curie": "UMLS:C0040799", "names": ["Aerodermectasia", "Subcutaneous emphysema", "Traumatic Subcutaneous Emphysema", "Traumatic subcutaneous emphysema", "traumatic subcutaneous emphysema", "Traumatic subcutaneous emphysema (disorder)", "traumatic subcutaneous emphysema (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Traumatic subcutaneous emphysema", "shortest_name_length": 15}
{"curie": "MONDO:0002170", "names": ["chronic otosalpingitis", "otosalpingitis, chronic", "Chronic eustachian salpingitis", "Chronic Eustachian salpingitis", "chronic eustachian salpingitis", "chronic eustachian tube salpingitis", "Chronic eustachian tube salpingitis", "chronic eustachian salpingitis (diagnosis)", "Chronic eustachian tube salpingitis (disorder)", "Chronic Eustachian salpingitis, unspecified ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic eustachian salpingitis", "shortest_name_length": 22}
{"curie": "MONDO:0002268", "names": ["dyspepsia", "Dyspepsia", "DYSPEPSIA", "Dyspepsias", "Indigestion", "INDIGESTION", "indigestion", "Indigestions", "Dyspepsia, NOS", "Indigestion, NOS", "Dyspepsia/indigestion", "dyspepsia (diagnosis)", "Indigestion (finding)", "dyspepsia, indigestion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyspepsia", "shortest_name_length": 9}
{"curie": "MONDO:0003584", "names": ["visual cortex disease", "Visual cortex disorder", "visual cortex disorder", "Visual Cortex Disorder", "disease of visual cortex", "Visual cortical disorder", "visual cortex dysfunction", "disorder of visual cortex", "Disorder of visual cortex", "Visual cortex dysfunction", "Cortical Visual Impairment", "disorders of visual cortex", "Disorders of visual cortex", "visual cortex disease or disorder", "Visual cortex dysfunction (finding)", "Disorder of visual cortex (disorder)", "disease (or disorder); visual cortex", "disease or disorder of visual cortex", "disease (or disorder); cortex, visual", "disorders of visual cortex (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "visual cortex disorder", "shortest_name_length": 21}
{"curie": "MONDO:0014170", "names": ["CDCBM3", "complex cortical dysplasia with other brain malformations 3", "cortical dysplasia, complex, with other brain malformations 3", "CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 3", "KIF2A complex cortical dysplasia with other brain malformations", "complex cortical dysplasia with other brain malformations type 3", "cortical dysplasia, Complex, with Other brain malformations type 3", "complex cortical dysplasia with other brain malformations caused by mutation in KIF2A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complex cortical dysplasia with other brain malformations 3", "shortest_name_length": 6}
{"curie": "UMLS:C1336488", "names": ["Stage I Supradiaphragmatic Nodular Lymphocyte Predominant Hodgkin Lymphoma", "Stage I Supradiaphragmatic Nodular Lymphocyte Predominant Hodgkin's Lymphoma", "Supradiaphragm Stage I Hodgkin's Lymphoma Nodular Lymphocyte Predominance Type", "Stage I Supradiaphragmatic Hodgkin Lymphoma Nodular Lymphocyte Predominant Type", "Stage I Supradiaphragmatic Hodgkin's Lymphoma Nodular Lymphocyte Predominant Type", "Stage I Supradiaphragmatic Hodgkin's Disease Nodular Lymphocyte Predominance Type", "Stage I Hodgkin's Disease Nodular Lymphocyte Predominance Type above the Diaphragm", "Stage I Hodgkin's Lymphoma Nodular Lymphocyte Predominance Type above the Diaphragm", "Ann Arbor Stage I Supradiaphragmatic Nodular Lymphocyte Predominant Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage I Supradiaphragmatic Nodular Lymphocyte Predominant Hodgkin Lymphoma", "shortest_name_length": 74}
{"curie": "UMLS:C0751436", "names": ["BH4 Deficiency", "Deficiency, BH4", "Hyperphenylalaninemia, type V", "Tetrahydrobiopterin deficiency", "Tetrahydrobiopterin Deficiency", "tetrahydrobiopterin deficiency", "Deficiency, Tetrahydrobiopterin", "Deficiency of tetrahydrobiopterin", "Tetrahydrobiopterin synthesis defect", "Tetrahydrobiopterin synthesis defect, NOS", "Non Phenylketonuric Hyperphenylalaninemia", "Non-phenylketonuric hyperphenylalaninemia", "Non-Phenylketonuric Hyperphenylalaninemia", "Non-Phenylketonuric Hyperphenylalaninemias", "Hyperphenylalaninemia, Non Phenylketonuric", "tetrahydrobiopterin deficiency (diagnosis)", "Hyperphenylalaninemia, Non-Phenylketonuric", "Hyperphenylalaninemia due to BH4 deficiency", "Tetrahydrobiopterin synthesis defect (disorder)", "Hyperphenylalaninemia due to tetrahydrobiopterin deficiency", "Hyperphenylalanineaemia due to tetrahydrobiopterin deficiency", "Hyperphenylalaninemia Caused by a Defect in Biopterin Metabolism", "Hyperphenylalaninemia due to BH4 (tetrahydrobiopterin) deficiency", "Hyperphenylalanineaemia due to BH4 (tetrahydrobiopterin) deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyperphenylalaninemia, Non-Phenylketonuric", "shortest_name_length": 14}
{"curie": "MONDO:0007084", "names": ["ALPF", "familial focal alopecia", "Alopecia, Familial Focal", "ALOPECIA, FAMILIAL FOCAL", "alopecia, familial focal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial focal alopecia", "shortest_name_length": 4}
{"curie": "MONDO:0044213", "names": ["Acute idiopathic urticaria", "acute idiopathic urticaria", "idiopathic urticaria, acute", "Acute idiopathic urticaria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute idiopathic urticaria", "shortest_name_length": 26}
{"curie": "MONDO:0007335", "names": ["OFC", "OFC1", "orofacial cleft 1", "orofacial cleft-1", "Orofacial Cleft 1", "OROFACIAL CLEFT 1", "orofacial cleft, nonsyndromic", "OROFACIAL CLEFT, NONSYNDROMIC", "Orofacial Cleft, Nonsyndromic", "cleft Lip/palate, nonsyndromic", "CLEFT LIP/PALATE, NONSYNDROMIC", "Cleft Lip-Palate, Nonsyndromic", "nonsyndromic cleft lip with or without cleft palate 1", "cleft lip with or without cleft palate, nonsyndromic, 1", "Cleft Lip with or without Cleft Palate, Nonsyndromic, 1", "CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orofacial cleft 1", "shortest_name_length": 3}
{"curie": "MONDO:0016459", "names": ["Del(2)(q23.1)", "monosomy 2q23.1", "Monosomy 2q23.1", "pseudo-Angelman syndrome", "Pseudo-Angelman syndrome", "2q23.1 microdeletion syndrome", "chromosome 2q23.1 microdeletion syndrome", "2q23.1 microdeletion syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "2q23.1 microdeletion syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0044138", "names": ["Hyalitis", "Vitritis", "VITRITIS", "hyalitis", "vitritis", "vitreitis", "Vitreitis", "hyaloiditis", "Hyaloiditis", "Hyalitis, NOS", "Vitritis, NOS", "Vitreocapsulitis", "vitreocapsulitis", "Vitritis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyalitis", "shortest_name_length": 8}
{"curie": "MONDO:0014508", "names": ["VMD4", "vitelliform macular dystrophy 4", "MACULAR DYSTROPHY, VITELLIFORM, 4", "macular dystrophy, vitelliform, 4", "IMPG1 vitelliform macular dystrophy", "macular dystrophy, vitelliform, type 4", "vitelliform macular dystrophy caused by mutation in IMPG1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitelliform macular dystrophy 4", "shortest_name_length": 4}
{"curie": "MONDO:0007878", "names": ["LARYNGOMALACIA", "Laryngomalacia", "laryngomalacia", "Laryngomalacias", "Larynx Chondromalacia", "Larynx Chondromalacias", "Chondromalacia of Larynx", "Congenital laryngomalacia", "laryngomalacia congenital", "Laryngomalacia (disorder)", "congenital laryngomalacia", "laryngomalacia (diagnosis)", "congenital laryngeal stridor", "Softening of voice box tissue", "Congenital laryngomalacia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital laryngomalacia", "shortest_name_length": 14}
{"curie": "MONDO:0100110", "names": ["adenovirus renal infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenovirus renal infection", "shortest_name_length": 26}
{"curie": "MONDO:0008794", "names": ["anhidrosis, familial generalized, with abnormal or absent sweat glands", "ANHIDROSIS, FAMILIAL GENERALIZED, WITH ABNORMAL OR ABSENT SWEAT GLANDS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anhidrosis, familial generalized, with abnormal or absent sweat glands", "shortest_name_length": 70}
{"curie": "MONDO:0013208", "names": ["HMDPC", "Hmdpc", "HMNDYT1", "HYPERMANGANESEMIA WITH DYSTONIA 1", "hypermanganesemia with dystonia 1", "hypermanganesemia with dystonia polycythemia and cirrhosis", "Hypermanganesemia with Dystonia Polycythemia and Cirrhosis", "Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome", "Hypermanganesemia with dystonia, polycythemia, and cirrhosis", "HYPERMANGANESEMIA WITH DYSTONIA, POLYCYTHEMIA, AND CIRRHOSIS", "Hypermanganesemia With Dystonia, Polycythemia, And Cirrhosis", "hypermanganesemia with dystonia, polycythemia, and cirrhosis", "Hypermanganesemia with dystonia, polycythaemia, and cirrhosis", "cirrhosis - dystonia - polycythemia - hypermanganesemia syndrome", "Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia", "Hepatic Cirrhosis, Dystonia, Polycythaemia, and Hypermanganesaemia", "HMDPC - hypermanganesemia with dystonia, polycythemia and cirrhosis", "HMDPC - hypermanganesemia with dystonia, polycythaemia and cirrhosis", "Hypermanganesemia with dystonia, polycythemia, and cirrhosis (disorder)", "Dystonia-Parkinsonism, Hypermanganesemia, Polycythemia, and Chronic Liver Disease", "Parkinsonism and Dystonia with Hypermanganesemia, Polycythemia, and Chronic Liver Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cirrhosis - dystonia - polycythemia - hypermanganesemia syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0009277", "names": ["GLC3A", "BUPHTHALMOS", "buphthalmia", "Buphthalmia", "buphthalmos", "glaucoma 3A", "Buphthalmos", "Buphthalmus", "Enlarged eyeball", "simple buphthalmos", "Simple buphthalmos", "glaucoma, congenital", "Buphthalmos (finding)", "Buphthalmos, unspecified", "Primary Congenital Glaucoma 3A", "Primary Congenital glaucoma 3A", "primary congenital glaucoma 3A", "GLAUCOMA 3, PRIMARY CONGENITAL A", "glaucoma 3, primary congenital, A", "GLAUCOMA 3, PRIMARY CONGENITAL, A", "Glaucoma 3, Primary Congenital, A", "glaucoma 3, primary congenital, type a", "glaucoma, primary open angle, adult-onset", "glaucoma, primary open angle, juvenile-onset", "GLAUCOMA, PRIMARY OPEN ANGLE, JUVENILE-ONSET", "glaucoma 3A, primary open angle, congenital, juvenile, or adult onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glaucoma 3A", "shortest_name_length": 5}
{"curie": "UMLS:C5555037", "names": ["Mucosal Melanoma of the Genitourinary System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mucosal Melanoma of the Genitourinary System", "shortest_name_length": 44}
{"curie": "MONDO:0004937", "names": ["Vitamin D excess", "D-hypervitaminosis", "d toxicity vitamin", "Hypervitaminosis D", "vitamin d toxicity", "hypervitaminosis d", "hypervitaminosis D", "HYPERVITAMINOSIS D", "vitamin D toxicity", "Vitamin D toxicity", "VITAMIN D TOXICITY", "hypervitaminosis; D", "Vitamin D poisoning", "vitamin d poisoning", "D; hypervitaminosis", "Vitamin D intoxication", "vitamin d intoxication", "Poisoning by vitamin D", "hypervitaminosis type D", "toxicity from vitamin D", "INTOXICATION, VITAMIN D", "hyperalimentation; vitamin D", "vitamin D; hyperalimentation", "Poisoning caused by vitamin D", "Hypervitaminosis D (disorder)", "vitamin D toxicity (diagnosis)", "hypervitaminosis D (diagnosis)", "Poisoning caused by vitamin D (disorder)", "HYPERVITAMINOSIS D VITAMIN D INTOXICATION", "HYPERVITAMINOSIS D <VITAMIN D INTOXICATION>"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypervitaminosis D", "shortest_name_length": 16}
{"curie": "UMLS:C3495920", "names": ["Lacrimal structural disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lacrimal structural disorder", "shortest_name_length": 28}
{"curie": "MONDO:0012782", "names": ["CELIAC13", "CELIAC DISEASE, SUSCEPTIBILITY TO, 13", "celiac disease, susceptibility to, 13", "GLUTEN-SENSITIVE ENTEROPATHY, SUSCEPTIBILITY TO, 13", "gluten-sensitive enteropathy, susceptibility to, 13"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "celiac disease, susceptibility to, 13", "shortest_name_length": 8}
{"curie": "MONDO:0014732", "names": ["HLD12", "VPS11 leukodystrophy", "hypomyelinating leukodystrophy 12", "leukodystrophy, hypomyelinating, 12", "LEUKODYSTROPHY, HYPOMYELINATING, 12", "hypomyelinating leukodystrophy type 12", "leukodystrophy, hypomyelinating, type 12", "leukodystrophy caused by mutation in VPS11", "VPS11-related autosomal recessive hypomyelinating leukodystrophy", "VPS11-related autosomal recessive hypomyelinating leukoencephalopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypomyelinating leukodystrophy 12", "shortest_name_length": 5}
{"curie": "MONDO:0005572", "names": ["polycythemia due to hypoxia", "Polycythemia due to hypoxia", "Polycythemia due to Hypoxia", "Polycythaemia due to hypoxia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polycythemia due to hypoxia", "shortest_name_length": 27}
{"curie": "MONDO:0044749", "names": ["XLCSNB", "X-linked CSNB", "X-linked congenital stationary night blindness", "congenital stationary night blindness, X-linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked congenital stationary night blindness", "shortest_name_length": 6}
{"curie": "MONDO:0032781", "names": ["CHEDDA", "CONGENITAL HYPOTONIA, EPILEPSY, DEVELOPMENTAL DELAY, AND DIGITAL ANOMALIES", "congenital hypotonia, epilepsy, developmental delay, and digital anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital hypotonia, epilepsy, developmental delay, and digital anomalies", "shortest_name_length": 6}
{"curie": "UMLS:C5230684", "names": ["NIFTP", "NIEFVPTC", "Follicular Thyroid Tumor", "Noninvasive Follicular Thyroid Neoplasm with Papillary-Like Nuclear Features", "Noninvasive Encapsulated Follicular Variant Papillary Thyroid Gland Carcinoma", "Non-invasive follicular thyroid neoplasm with papillary like nuclear features", "Noninvasive Encapsulated Follicular Variant Thyroid Gland Papillary Carcinoma", "Thyroid Gland Noninvasive Follicular Tumor with Papillary-Like Nuclear Features", "Thyroid Gland Noninvasive Follicular Neoplasm with Papillary-Like Nuclear Features", "Noninvasive Follicular Thyroid Gland Neoplasm with Papillary-Like Nuclear Features", "NIFTP - non-invasive follicular thyroid neoplasm with papillary like nuclear features", "Non-invasive follicular thyroid neoplasm with papillary-like nuclear features (NIFTP)", "Non-invasive follicular thyroid neoplasm with papillary like nuclear features (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-invasive follicular thyroid neoplasm with papillary like nuclear features", "shortest_name_length": 5}
{"curie": "MONDO:0003839", "names": ["Mucinous adenocarcinofibroma", "Ovarian Mucinous Adenocarcinofibroma", "ovarian mucinous adenocarcinofibroma", "mucinous adenocarcinofibroma of ovary", "ovarian mucinous malignant adenofibroma", "Ovarian Mucinous Malignant Adenofibroma", "mucinous adenocarcinofibroma of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian mucinous adenocarcinofibroma", "shortest_name_length": 28}
{"curie": "EFO:0011053", "names": ["immune system toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immune system toxicity", "shortest_name_length": 22}
{"curie": "MONDO:0018564", "names": ["Del(3)p(25.3)", "monosomy 3p25.3", "3p25.3 microdeletion syndrome", "intellectual disability-epilepsy-stereotypic hand movement syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "3p25.3 microdeletion syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0009232", "names": ["FUHRMANN SYNDROME", "Fuhrmann syndrome", "Fuhrmann syndrome (disorder)", "Fuhrmann Rieger de Sousa syndrome", "Fuhrmann-Rieger-de Sousa syndrome", "Fibular hypoplasia or aplasia-femoral bowing-oligodactyly syndrome", "fibular hypoplasia or aplasia-femoral bowing-oligodactyly syndrome", "fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly", "FIBULAR APLASIA OR HYPOPLASIA, FEMORAL BOWING AND POLY-, SYN-, AND OLIGODACTYLY", "bowing of the femurs, aplasia or hypoplasia of the fibula, and digital anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fuhrmann syndrome", "shortest_name_length": 17}
{"curie": "MONDO:0000129", "names": ["Glutaricaciduria", "glutaric acidemia", "glutaric aciduria", "aciduria glutaric", "Glutaric aciduria", "glutaric; aciduria", "Glutarate aciduria", "aciduria; glutaric", "Glutaric aciduria NOS", "Glutaric aciduria, NOS", "glutaric aciduria (disease)", "Glutaric aciduria (disorder)", "Increased glutarate level in urine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glutaric aciduria", "shortest_name_length": 16}
{"curie": "MONDO:0022734", "names": ["chorioretinopathy dominant form microcephaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chorioretinopathy dominant form microcephaly", "shortest_name_length": 44}
{"curie": "MONDO:0009675", "names": ["LGMD2", "LGMD2A", "LGMDR1", "LGMD type 2A", "calpainopathy", "Calpainopathy", "CALPAINOPATHY", "primary calpainopathy", "Eosinophilic myositis", "Primary calpainopathy", "Myositis, Eosinophilic", "myositis, eosinophilic", "MYOSITIS, EOSINOPHILIC", "LGMD R1 calpain-3-related", "Calpain-3-related LGMD R1", "pelvofemoral muscular dystrophy", "Leyden-Möbius muscular dystrophy", "Eosinophilic myositis (disorder)", "Muscular dystrophy, pelvofemoral", "MUSCULAR DYSTROPHY, PELVOFEMORAL", "muscular dystrophy, Pelvofemoral", "Leyden-Moebius muscular dystrophy", "LEYDEN-MOEBIUS MUSCULAR DYSTROPHY", "limb-girdle muscular dystrophy type 2", "Limb-girdle muscular dystrophy type 2", "muscular dystrophy, limb-girdle Type 2", "Limb-Girdle Muscular Dystrophy Type 2A", "limb-girdle muscular dystrophy type 2A", "Limb-girdle muscular dystrophy type 2A", "Limb girdle muscular dystrophy type 2A", "muscular dystrophy, limb-girdle, type 2", "Muscular Dystrophy, Limb-Girdle, Type 2", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2A", "Muscular Dystrophy, Limb-Girdle, Type 2A", "muscular dystrophy, limb-girdle, type 2A", "muscular dystrophy limb girdle type 2A, erb type", "muscular dystrophy, limb-girdle Type 2 (diagnosis)", "Calpain-3-related limb-girdle muscular dystrophy R1", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 1", "muscular dystrophy, limb-girdle, autosomal recessive 1", "CAPN3 autosomal recessive limb-girdle muscular dystrophy", "Limb-girdle muscular dystrophy due to calpain deficiency", "limb-girdle muscular dystrophy due to calpain deficiency", "Autosomal recessive limb-girdle muscular dystrophy type 2A", "Autosomal recessive limb girdle muscular dystrophy type 2A", "autosomal recessive limb-girdle muscular dystrophy type 2A", "Calpain-3 deficiency limb girdle muscular dystrophy type 2A", "Autosomal recessive limb girdle muscular dystrophy type 2A (disorder)", "autosomal recessive limb-girdle muscular dystrophy caused by mutation in CAPN3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive limb-girdle muscular dystrophy type 2A", "shortest_name_length": 5}
{"curie": "MONDO:0007105", "names": ["FTDMND", "FTDALS", "ALSFTD", "FTD-ALS", "FTDALS1", "FTD-MND", "Frontotemporal dementia with motor neuron disease", "Frontotemporal Dementia With Motor Neuron Disease", "frontotemporal dementia and/or motor neuron disease", "FRONTOTEMPORAL DEMENTIA AND/OR MOTOR NEURON DISEASE", "Frontotemporal Dementia-Amyotrophic Lateral Sclerosis", "C9ORF72 frontotemporal dementia with motor neuron disease", "C9orf72 frontotemporal dementia with motor neuron disease", "Amyotrophic lateral sclerosis with frontotemporal dementia", "Frontotemporal dementia with amyotrophic lateral sclerosis", "frontotemporal dementia and/or amyotrophic lateral sclerosis", "Amyotrophic Lateral Sclerosis And-Or Frontotemporal Dementia", "AMYOTROPHIC LATERAL SCLEROSIS AND/OR FRONTOTEMPORAL DEMENTIA", "amyotrophic lateral sclerosis and/or frontotemporal dementia", "FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS", "Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1", "FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 1", "frontotemporal dementia and/or amyotrophic lateral sclerosis-1", "frontotemporal dementia and/or amyotrophic lateral sclerosis 1", "frontotemporal dementia and/or amyotrophic lateral sclerosis type 1", "Amyotrophic lateral sclerosis with frontotemporal dementia (disorder)", "frontotemporal dementia with motor neuron disease caused by mutation in C9orf72", "frontotemporal dementia with motor neuron disease caused by mutation in C9ORF72"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontotemporal dementia and/or amyotrophic lateral sclerosis 1", "shortest_name_length": 6}
{"curie": "MONDO:0023035", "names": ["Eagle syndrome", "Eagle's syndrome", "Styloid-stylohoid syndrome", "styloid-stylohoid syndrome", "elongated styloid process syndrome", "Elongated styloid process syndrome", "Elongated styloid process syndrome (disorder)", "elongated styloid process syndrome (diagnosis)", "elongated styloid process which causes cervico facial pain tinnitus and otalgia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eagle syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0008443", "names": ["SPASTIC PARAPLEGIA WITH PRECOCIOUS PUBERTY", "spastic paraplegia with precocious puberty", "PRECOCIOUS PUBERTY WITH SPASTIC PARAPLEGIA", "precocious puberty with spastic paraplegia", "Precocious puberty with spastic paraplegia", "Spastic paraplegia with precocious puberty", "spastic paraplegia-precocious puberty syndrome", "Familial spastic paraplegia, mental retardation, and precocious puberty", "familial spastic paraplegia, mental retardation, and precocious puberty", "familial spastic paraplegia, intellectual disability, and precocious puberty"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic paraplegia-precocious puberty syndrome", "shortest_name_length": 42}
{"curie": "MONDO:0700174", "names": ["horse transitional cell carcinoma", "Horse Transitional Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "horse transitional cell carcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C0919715", "names": ["lupus-like syndrome", "Lupus-like syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lupus-like syndrome", "shortest_name_length": 19}
{"curie": "UMLS:C0542008", "names": ["Hematoma injection site", "Injection site hematoma", "HEMATOMA INJECTION SITE", "Injection site haematoma", "Haematoma injection site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site hematoma", "shortest_name_length": 23}
{"curie": "MONDO:0031421", "names": ["OLMS", "Olmsted syndrome", "Olmstead syndrome", "Olmstead syndrome (diagnosis)", "palmoplantar and periorificial keratoderma", "Palmoplantar and periorificial keratoderma", "Congenital palmoplantar and perioral keratoderma of Olmsted", "Congenital palmoplantar and perioral keratoderma of Olmsted (disorder)", "Mutilating palmoplantar keratoderma with periorificial keratotic plaques", "mutilating palmoplantar keratoderma with periorificial keratotic plaques", "palmoplantar keratoderma, mutilating, with periorificial keratotic plaques", "Mutilating palmoplantar hyperkeratosis with periorificial keratotic plaques", "mutilating palmoplantar hyperkeratosis with periorificial keratotic plaques"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Olmsted syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0005026", "names": ["Endometrioid carcinoma", "ENDOMETRIOID CARCINOMA", "carcinoma endometrioid", "Endometrioid Carcinoma", "endometrioid carcinoma", "Carcinoma, Endometrioid", "Endometrioid Carcinomas", "Carcinomas, Endometrioid", "Endometrioid carcinoma, NOS", "Endometrioid adenocarcinoma", "Endometrioid Adenocarcinoma", "endometrioid adenocarcinoma", "Endometrioid Adenocarcinomas", "Adenocarcinoma, Endometrioid", "Adenocarcinomas, Endometrioid", "Endometrioid cystadenocarcinoma", "Endometrioid adenocarcinoma, NOS", "endometrioid carcinoma (diagnosis)", "female reproductive endometrioid carcinoma", "Endometrioid carcinoma (morphologic abnormality)", "carcinoma; endometrioid, unspecified site, female", "endometrioid; carcinoma, unspecified site, female", "endometrioid carcinoma of female reproductive system", "endometrioid carcinoma of the female reproductive system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometrioid adenocarcinoma", "shortest_name_length": 22}
{"curie": "UMLS:C0346062", "names": ["Smooth Muscle Skin Neoplasm", "Skin Smooth Muscle Neoplasm", "Cutaneous Smooth Muscle Neoplasm", "Skin tumor of smooth muscle origin", "Skin Tumor of Smooth Muscle Origin", "Skin tumour of smooth muscle origin", "Skin Neoplasm of Smooth Muscle Origin", "Cutaneous Tumor of Smooth Muscle Origin", "Cutaneous Neoplasm of Smooth Muscle Origin", "Skin tumor of smooth muscle origin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin tumor of smooth muscle origin", "shortest_name_length": 27}
{"curie": "UMLS:C4524646", "names": ["Esophageal Squamous Cell Carcinoma by AJCC v8 ypTNM Stage", "Esophageal Squamous Cell Carcinoma by AJCC v8 Postneoadjuvant Therapy Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Squamous Cell Carcinoma by AJCC v8 Postneoadjuvant Therapy Stage", "shortest_name_length": 57}
{"curie": "UMLS:C4329643", "names": ["Cerebellar and Brain Stem Ependymal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebellar and Brain Stem Ependymal Tumor", "shortest_name_length": 41}
{"curie": "MONDO:0003865", "names": ["ALM", "Acral Melanoma", "acral melanoma", "subungual melanoma", "palmar/plantar melanoma", "Acral Lentiginous Melanoma", "acral lentiginous melanoma", "Acral lentiginous melanoma", "Melanoma, acral lentiginous", "acral lentiginous melanoma of skin", "Acral lentiginous melanoma of skin", "acral lentiginous malignant melanoma", "acral lentiginous melanoma (disease)", "malignant acral lentiginous melanoma", "Malignant acral lentiginous melanoma", "Acral Lentiginous Malignant Melanoma", "melanoma, acral lentiginous malignant", "Acral lentiginous melanoma, malignant", "acral lentiginous melanoma, malignant", "malignant melanoma, acral lentiginous", "ALM - Acral lentiginous melanoma of skin", "[M] Acral lentiginous melanoma, malignant", "Acral lentiginous malignant melanoma of skin", "acral lentiginous malignant melanoma of skin", "acral lentiginous melanoma of skin (diagnosis)", "ALMM - Acral lentiginous malignant melanoma of skin", "Acral lentiginous malignant melanoma of skin (disorder)", "Acral lentiginous melanoma, malignant (morphologic abnormality)", "acral lentiginous melanoma, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acral lentiginous melanoma", "shortest_name_length": 3}
{"curie": "UMLS:C1266174", "names": ["Sarcomatoid Chordoma", "Dedifferentiated chordoma", "Dedifferentiated Chordoma", "dedifferentiated chordoma", "dedifferentiated chordoma (diagnosis)", "Dedifferentiated chordoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dedifferentiated chordoma", "shortest_name_length": 20}
{"curie": "MONDO:0006442", "names": ["tendon sheath fibroma", "Tendon Sheath Fibroma", "Fibroma of tendon sheath", "Fibroma of Tendon Sheath", "fibroma of tendon sheath", "Fibroma of the Tendon Sheath", "fibroma of the tendon sheath", "Fibroma of tendon sheath (disorder)", "Fibroma of tendon sheath (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tendon sheath fibroma", "shortest_name_length": 21}
{"curie": "UMLS:C0263437", "names": ["acne neonatal", "neonatal acne", "Neonatal acne", "infantile acne", "acne infantile", "Acne, neonatal", "Acne infantile", "Infantile acne", "Acne neonatorum", "acne neonatorum", "Neonatal acne (disorder)", "neonatal acne (diagnosis)", "Infantile acne (disorder)", "infantile acne (diagnosis)", "neonatal acne (physical finding)", "clinical impressions neonatal acne"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infantile acne", "shortest_name_length": 13}
{"curie": "UMLS:C3897507", "names": ["Stage IVC Thyroid Gland Follicular Cancer", "Stage IVC Thyroid Gland Follicular Carcinoma", "Stage IVC Thyroid Gland Follicular Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Thyroid Gland Follicular Carcinoma AJCC v7", "shortest_name_length": 41}
{"curie": "MONDO:0003459", "names": ["cervical adenofibroma", "Cervical Adenofibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical adenofibroma", "shortest_name_length": 21}
{"curie": "UMLS:C5206481", "names": ["Metastatic Colorectal Mucinous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Colorectal Mucinous Adenocarcinoma", "shortest_name_length": 45}
{"curie": "MONDO:0007859", "names": ["KPPS1", "PPKS1", "SPPK1", "STRIATE PALMOPLANTAR KERATODERMA I", "Striate Palmoplantar Keratoderma I", "KERATOSIS PALMOPLANTARIS STRIATA I", "Keratosis palmoplantaris striata 1", "keratosis palmoplantaris striata 1", "Keratosis Palmoplantaris Striata I", "Striate palmoplantar keratoderma 1", "striate palmoplantar keratoderma 1", "PALMOPLANTAR KERATODERMA I, STRIATE", "keratosis palmoplantaris striata i, AD", "keratoderma, palmoplantar striate form 1", "Keratoderma, palmoplantar striate form 1", "Keratoderma, Palmoplantar, Striate Form I", "keratoderma, palmoplantar, striate form 1", "KERATODERMA, PALMOPLANTAR, STRIATE FORM I", "palmoplantar keratoderma I, striate, focal, or diffuse", "palmoplantar keratoderma i, striate, focal, or diffuse", "PALMOPLANTAR KERATODERMA I, STRIATE, FOCAL, OR DIFFUSE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "palmoplantar keratoderma i, striate, focal, or diffuse", "shortest_name_length": 5}
{"curie": "UMLS:C5204289", "names": ["Pseudohyperplastic Carcinoma of the Penis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pseudohyperplastic Carcinoma of the Penis", "shortest_name_length": 41}
{"curie": "MONDO:0015769", "names": ["trisomy 6pter", "Trisomy 6pter", "distal trisomy 6p", "Distal trisomy 6p", "Distal duplication 6p", "distal duplication 6p", "distal trisomy type 6p", "telomeric duplication 6p", "Telomeric duplication 6p", "Distal trisomy 6p syndrome", "Distal trisomy 6p syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal trisomy 6p", "shortest_name_length": 13}
{"curie": "MONDO:0002794", "names": ["medulloblastoma", "Medulloblastoma", "Adult Medulloblastoma", "adult medulloblastoma", "adults medulloblastoma", "medulloblastoma, adult", "Medulloblastoma, Adult", "Adult Medulloblastomas", "Medulloblastomas, Adult", "medulloblastoma of adults", "adult brain medulloblastoma", "Adult Brain Medulloblastoma", "adult CNS tumor, medulloblastoma", "CNS tumor, adult medulloblastoma", "CNS tumor, medulloblastoma, adult", "adult brain tumor, medulloblastoma", "brain tumor, adult medulloblastoma", "central nervous system tumor, medulloblastoma, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult medulloblastoma", "shortest_name_length": 15}
{"curie": "MONDO:0018770", "names": ["ATD", "JATD", "Jeune", "jeune syndrome", "Jeune Syndrome", "Jeune syndrome", "JEUNE SYNDROME", "jeunes syndrome", "jeune's syndrome", "Jeune's syndrome", "Jeune thoracic dysplasia", "Jeune Thoracic Dysplasia", "Jeune thoracic dystrophy", "jeune thoracic dystrophy", "Jeune Thoracic Dystrophy", "infantile thoracic dystrophy", "short-rib thoracic dysplasia", "Infantile thoracic dystrophy", "thoracic asphyxiant dystrophy", "Thoracic Asphyxiant Dystrophy", "Asphyxiating thoracic dystrophy", "Asphyxiating thoracic dysplasia", "Asphyxiating Thoracic Dystrophy", "asphyxiating thoracic dysplasia", "Asphyxiating Thoracic Dysplasia", "asphyxiating thoracic dystrophy", "Jeune thoracic dystrophy (disorder)", "Jeune's thoracic dystrophy syndrome", "thoracic pelvic phalangeal dystrophy", "THORACIC-PELVIC-PHALANGEAL DYSTROPHY", "thoracic-pelvic-phalangeal dystrophy", "Thoracic pelvic phalangeal dystrophy", "Thoracic-Pelvic-Phalangeal Dystrophy", "Asphyxiating Thoracic Dystrophy (ATD)", "Jeune asphyxiating thoracic dystrophy", "asphyxiating thoracic dystrophy (ATD)", "asphyxiating thoracic chondrodystrophy", "Asphyxiating Thoracic Chondrodystrophy", "chondroectodermal dysplasia-like syndrome", "Chondroectodermal dysplasia-like syndrome", "Asphyxiating thoracic dystrophy (diagnosis)", "asphyxiating thoracic dystrophy of the newborn", "Asphyxiating thoracic dystrophy of the newborn", "short-rib thoracic dysplasia with or without polydactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jeune syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0009776", "names": ["SPGF1", "SPERMATOGENIC FAILURE 1", "spermatogenic failure 1", "Oligosynaptic infertility", "Oligochiasmic infertility", "OLIGOSYNAPTIC INFERTILITY", "oligosynaptic infertility", "Oligosynaptic Infertility", "Oligochiasmic Infertility", "OLIGOCHIASMATIC INFERTILITY", "oligochiasmatic infertility", "Oligochiasmatic infertility", "Oligosynaptic infertility (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 1", "shortest_name_length": 5}
{"curie": "MONDO:0017746", "names": ["Atypical RTT", "atypical RTT", "Rett like syndrome", "Rett syndrome variant", "Rett syndrome atypical", "atypical Rett syndrome", "Atypical Rett syndrome", "Rett Syndrome, Atypical", "RETT SYNDROME, ATYPICAL", "Atypical Rett syndrome (disorder)", "Atypical Rett syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical Rett syndrome", "shortest_name_length": 12}
{"curie": "UMLS:C4763883", "names": ["Enterotoxigenic E coli Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Enterotoxigenic E coli Infection", "shortest_name_length": 32}
{"curie": "UMLS:C5238249", "names": ["Recurrent Diffuse Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Diffuse Astrocytoma", "shortest_name_length": 29}
{"curie": "MONDO:0004243", "names": ["Vulvar Proximal-Type Epithelioid Sarcoma", "vulvar proximal-type epithelioid sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar proximal-type epithelioid sarcoma", "shortest_name_length": 40}
{"curie": "MONDO:0006523", "names": ["Acrodermatitis", "ACRODERMATITIS", "acrodermatitis", "Acrodermatitides", "Acrodermatitis, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acrodermatitis", "shortest_name_length": 14}
{"curie": "MONDO:0018255", "names": ["spondylometaphyseal dysplasia, Czarny-Ratajczak type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondylometaphyseal dysplasia, Czarny-Ratajczak type", "shortest_name_length": 52}
{"curie": "UMLS:C4526653", "names": ["Pleural Malignant Mesothelioma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pleural Malignant Mesothelioma by AJCC v8 Stage", "shortest_name_length": 47}
{"curie": "UMLS:C5446520", "names": ["Refractory Extrahepatic Bile Duct Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Extrahepatic Bile Duct Carcinoma", "shortest_name_length": 43}
{"curie": "UMLS:C4525730", "names": ["Cortical Cataract Grade 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cortical Cataract Grade 4", "shortest_name_length": 25}
{"curie": "UMLS:C5448014", "names": ["Metastatic Malignant Neoplasm in the Lacrimal System", "Metastatic Malignant Neoplasm in the Lacrimal Apparatus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Malignant Neoplasm in the Lacrimal System", "shortest_name_length": 52}
{"curie": "MONDO:0006649", "names": ["aion", "optic nerve ischemia", "Optic Nerve Ischemia", "Ischemia, Optic Nerve", "Optic Nerve Ischemias", "Nerve Ischemia, Optic", "OPTIC NEUROPATHY ISCHEMIC", "Optic Ischemic Neuropathy", "ischemic optic neuropathy", "ischemic neuropathy optic", "Ischemic optic neuropathy", "Ischemic Optic Neuropathy", "Optic ischemic neuropathy", "Neuropathy, Ischemic Optic", "Optic Ischaemic Neuropathy", "Optic Neuropathy, Ischemic", "ischaemic optic neuropathy", "Ischaemic optic neuropathy", "Optic ischaemic neuropathy", "Ischemic Neuropathy, Optic", "Neuropathy, Optic Ischemic", "Ischemic Optic Neuropathies", "Optic Ischemic Neuropathies", "Neuropathy, Optic Ischaemic", "Ischaemic Neuropathy, Optic", "Optic Ischaemic Neuropathies", "ION - Ischemic optic neuropathy", "ION - Ischaemic optic neuropathy", "Anterior ischemic optic neuropathy", "anterior ischemic optic neuropathy", "ischemic optic neuropathy anterior", "ischemic; neuropathic, optic nerve", "Anterior Ischemic Optic Neuropathy", "Optic Neuropathy, Anterior Ischemic", "Anterior ischaemic optic neuropathy", "Ischemic optic neuropathy (disorder)", "ischemic optic neuropathy (diagnosis)", "AION - Acute ischemic optic neuropathy", "AION - Acute ischaemic optic neuropathy", "AION - anterior ischemic optic neuropathy", "AION - anterior ischaemic optic neuropathy", "optic disc infarction leading to vision loss", "Anterior ischemic optic neuropathy (disorder)", "Anterior ischemic optic neuropathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anterior ischemic optic neuropathy", "shortest_name_length": 4}
{"curie": "UMLS:C5204451", "names": ["Light Chain Fanconi Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Light Chain Fanconi Syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0013529", "names": ["CPVT3", "CVPT3", "catecholaminergic polymorphic ventricular tachycardia 3", "ventricular tachycardia, catecholaminergic polymorphic, 3", "VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 3", "TECRL catecholaminergic polymorphic ventricular tachycardia", "catecholaminergic polymorphic ventricular tachycardia type 3", "Catecholaminergic Polymorphic Ventricular Tachycardia Type 3", "catecholaminergic polymorphic ventricular tachycardia caused by mutation in TECRL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "catecholaminergic polymorphic ventricular tachycardia 3", "shortest_name_length": 5}
{"curie": "MONDO:0700156", "names": ["Canine Soft Tissue Sarcoma", "canine soft tissue sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canine soft tissue sarcoma", "shortest_name_length": 26}
{"curie": "UMLS:C5557153", "names": ["Stage IA2 Cervical Cancer AJCC v9", "Stage IA2 Cervical Carcinoma AJCC v9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA2 Cervical Cancer AJCC v9", "shortest_name_length": 33}
{"curie": "MONDO:0016497", "names": ["paraparetic variant of GBS", "paraparetic variant of Guillain-Barre syndrome", "paraparetic variant of Guillain-Barré syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paraparetic variant of Guillain-Barre syndrome", "shortest_name_length": 26}
{"curie": "MONDO:0031009", "names": ["GT2", "BDPLT23", "GLANZMANN THROMBASTHENIA 2", "Glanzmann thrombasthenia 2", "bleeding disorder, platelet-type, 23", "BLEEDING DISORDER, PLATELET-TYPE, 23"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Glanzmann thrombasthenia 2", "shortest_name_length": 3}
{"curie": "MONDO:0024410", "names": ["Bifidobacterium infection", "Bifidobacterium infectious disease", "Bifidobacterium disease or disorder", "infection caused by Bifidobacterium", "Infection caused by Bifidobacterium", "Bifidobacterium caused disease or disorder", "Infection caused by Bifidobacterium (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infection caused by Bifidobacterium", "shortest_name_length": 25}
{"curie": "UMLS:C2981701", "names": ["stage IIIA eyelid carcinoma", "Stage IIIA Eyelid Carcinoma", "Stage IIIA Eyelid Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Eyelid Carcinoma AJCC v7", "shortest_name_length": 27}
{"curie": "MONDO:0011395", "names": ["CORD3", "CONE-ROD DYSTROPHY 3", "Cone-Rod Dystrophy 3", "cone-rod dystrophy 3", "ABCA4 cone-rod dystrophy", "cone-rod dystrophy type 3", "CONE-ROD DYSTROPHY 3 (disorder)", "cone-rod dystrophy caused by mutation in ABCA4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cone-rod dystrophy 3", "shortest_name_length": 5}
{"curie": "MONDO:0034987", "names": ["intraductal tubulopapillary neoplasm of pancreas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intraductal tubulopapillary neoplasm of pancreas", "shortest_name_length": 48}
{"curie": "UMLS:C1333267", "names": ["Deep Lipoma", "Deep Fatty Tumor", "Deep Fatty Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Deep Lipoma", "shortest_name_length": 11}
{"curie": "MONDO:0015247", "names": ["OMS", "OMA syndrome", "oma syndrome", "POMA syndrome", "Kinsbourne syndrome", "dancing eye syndrome", "Dancing eye syndrome", "Opsoclonus Myoclonus Ataxia", "Opsoclonus-myoclonus syndrome", "Opsoclonus Myoclonus Syndrome", "Opsoclonus-Myoclonus Syndrome", "opsoclonus-myoclonus syndrome", "opsoclonus myoclonus syndrome", "Ataxo-opso-myoclonus syndrome", "Dancing eye-dancing feet syndrome", "dancing eye-dancing feet syndrome", "Dancing Eyes-Dancing Feet Syndrome", "Dancing Eyes Dancing Feet Syndrome", "paraneoplastic opsoclonus-myoclonus", "Dancing Eyes, Dancing Feet Syndrome", "Paraneoplastic opsoclonus-myoclonus", "opsoclonus-myoclonus-ataxia syndrome", "Opsoclonus-myoclonus-ataxia syndrome", "Opsoclonus-myoclonus syndrome (disorder)", "Paraneoplastic opsoclonus-myoclonus-ataxia syndrome", "paraneoplastic opsoclonus-myoclonus-ataxia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "opsoclonus-myoclonus syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0024953", "names": ["Animal Lameness", "animal lameness", "Lameness, Animal", "animal Lamenesses", "Animal Lamenesses", "Lamenesses, Animal", "Lamenesses, animal", "Animal Gait Disorder", "animal Gait disorder", "Disorder, Animal Gait", "Gait disorder, animal", "Animal Gait Disorders", "Gait Disorder, Animal", "animal Gait disorders", "disorder, animal Gait", "Gait disorders, animal", "Gait Disorders, Animal", "disorders, animal Gait", "Disorders, Animal Gait", "lameness, non-human animal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lameness, non-human animal", "shortest_name_length": 15}
{"curie": "UMLS:C2983845", "names": ["Stage 0 Uterine Corpus Cancer AJCC v6", "Endometrial Carcinoma in situ AJCC v6", "Stage 0 Uterine (including Endometrial) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Uterine Corpus Cancer AJCC v6", "shortest_name_length": 37}
{"curie": "UMLS:C1392786", "names": ["Cognitive Change", "cognitive; change", "change; cognitive", "Cognitive changes", "Cognitive Changes", "Cognitive Alteration", "Alteration In Cognition", "Alteration Of Cognitive Function", "Alteration in cognitive functioning"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cognitive changes", "shortest_name_length": 16}
{"curie": "UMLS:C5556680", "names": ["Unresectable Thymic Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Thymic Neuroendocrine Neoplasm", "shortest_name_length": 43}
{"curie": "UMLS:C1336164", "names": ["Stage IIA Lung Cancer", "Stage IIA Lung Carcinoma", "Stage IIA Carcinoma of Lung", "Stage IIA Lung Cancer AJCC v7", "Stage IIA Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Lung Cancer AJCC v7", "shortest_name_length": 21}
{"curie": "UMLS:C4288921", "names": ["Idiopathic Membranous Glomerulopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Idiopathic Membranous Glomerulopathy", "shortest_name_length": 36}
{"curie": "MONDO:0021631", "names": ["brain astrocytoma", "Brain Astrocytoma", "BRAIN, ASTROCYTOMA", "Astrocytoma of brain", "BRAIN TUMOR, ASTROCYTOMA", "CANCER, BRAIN ASTROCYTOMA", "Astrocytic tumor of brain", "Astrocytic tumour of brain", "Astrocytoma of brain (disorder)", "Astrocytoma of brain (diagnosis)", "brain tumor malignant astrocytoma", "INTRACRANIAL NEOPLASM, ASTROCYTOMA", "brain astrocytoma (excluding glioblastoma)", "astrocytoma (excluding glioblastoma) of brain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brain astrocytoma", "shortest_name_length": 17}
{"curie": "MONDO:0001763", "names": ["ethmoid sinus cancer", "cancer of ethmoid sinus", "Malignant Ethmoid Sinus Tumor", "malignant ethmoid sinus tumor", "Malignant Ethmoidal Sinus Tumor", "malignant ethmoidal sinus tumor", "Malignant Ethmoid Sinus Neoplasm", "Malignant tumor of ethmoid sinus", "Malignant Tumor of Ethmoid Sinus", "malignant tumor of ethmoid sinus", "malignant ethmoid sinus neoplasm", "Malignant tumour of ethmoid sinus", "malignant ethmoidal sinus neoplasm", "Malignant Tumor of Ethmoidal Sinus", "Malignant Ethmoidal Sinus Neoplasm", "malignant tumor of ethmoidal sinus", "Malignant Neoplasm of Ethmoid Sinus", "malignant neoplasm of ethmoid sinus", "Malignant neoplasm of ethmoid sinus", "malignant tumor of the ethmoid sinus", "Malignant Tumor of the Ethmoid Sinus", "Malignant neoplasm of ethmoidal sinus", "malignant neoplasm of ethmoidal sinus", "Malignant Neoplasm of Ethmoidal Sinus", "Malignant Tumor of the Ethmoidal Sinus", "malignant tumor of the ethmoidal sinus", "malignant neoplasm of the ethmoid sinus", "Malignant Neoplasm of the Ethmoid Sinus", "malignant neoplasm of the ethmoidal sinus", "Malignant Neoplasm of the Ethmoidal Sinus", "Malignant tumor of ethmoid sinus (disorder)", "malignant neoplasm of ethmoid sinus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ethmoid sinus cancer", "shortest_name_length": 20}
{"curie": "MONDO:0019884", "names": ["Trisomy 10qter", "trisomy 10qter", "Distal trisomy 10q", "distal trisomy 10q", "Distal duplication 10q", "distal duplication 10q", "distal trisomy type 10q", "Telomeric duplication 10q", "telomeric duplication 10q", "Distal Trisomy 10q Syndrome", "Distal trisomy 10q (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal trisomy 10q", "shortest_name_length": 14}
{"curie": "UMLS:C1334054", "names": ["HPV-Related Esophageal Squamous Cell Carcinoma", "Human Papillomavirus-Related Esophageal Squamous Cell Carcinoma", "Human Papilloma Virus Related Esophageal Squamous Cell Carcinoma", "Human Papilloma Virus-Related Esophageal Squamous Cell Carcinoma", "Human Papillomavirus (HPV)-Related Esophageal Squamous Cell Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Human Papillomavirus-Related Esophageal Squamous Cell Carcinoma", "shortest_name_length": 46}
{"curie": "MONDO:0007053", "names": ["RLS1", "EKBOM SYNDROME", "Ekbom syndrome", "Acromelalgia hereditary", "acromelalgia, hereditary", "Restless legs syndrome 1", "ACROMELALGIA, HEREDITARY", "RESTLESS LEGS SYNDROME, SUSCEPTIBILITY TO, 1", "restless legs syndrome, susceptibility to, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "restless legs syndrome, susceptibility to, 1", "shortest_name_length": 4}
{"curie": "UMLS:C5419823", "names": ["Extrahepatic Bile Duct Neuroendocrine Tumor G3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extrahepatic Bile Duct Neuroendocrine Tumor G3", "shortest_name_length": 46}
{"curie": "MONDO:0010420", "names": ["XLP", "XLPP", "Xldpt", "XLEPP", "XLDPP", "X-Linked Protoporphyria", "X-linked dominant protoporphyria", "X-linked erythropoietic protoporphyria", "ERYTHROHEPATIC PROTOPORPHYRIA, X-LINKED", "Erythrohepatic protoporphyria, X-linked", "erythropoietic protoporphyria, X-linked", "Erythrohepatic Protoporphyria, X-Linked", "PROTOPORPHYRIA, ERYTHROPOIETIC, X-LINKED", "protoporphyria, erythropoietic, X-linked", "X-linked dominant erythropoietic protoporphyria", "Protoporphyria, Erythropoietic, X-Linked Dominant", "protoporphyria, erythropoietic, X-linked dominant", "PROTOPORPHYRIA, ERYTHROPOIETIC, X-LINKED DOMINANT", "X-linked dominant erythropoietic protoporphyria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked erythropoietic protoporphyria", "shortest_name_length": 3}
{"curie": "MONDO:0006641", "names": ["Afferent Loop Syndrome", "afferent loop syndrome", "Afferent loop syndrome", "AFFERENT LOOP SYNDROME", "Afferent limb syndrome", "Syndrome, Afferent Loop", "syndrome; afferent loop", "Afferent Loop Syndromes", "afferent; loop syndrome", "Loop Syndrome, Afferent", "Syndromes, Afferent Loop", "Loop Syndromes, Afferent", "Blind duodenal loop syndrome", "Afferent loop syndrome (disorder)", "Gastrojejunal loop obstruction syndrome", "gastric surgery; afferent loop syndrome", "GASTROJEJUNAL LOOP OBSTRUCTION SYNDROME", "syndrome; gastrojejunal loop obstruction", "gastrojejunal loop obstruction; syndrome", "syndrome; afferent loop, postgastric surgery", "afferent; loop syndrome, postgastric surgery"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "afferent loop syndrome", "shortest_name_length": 22}
{"curie": "UMLS:C0032805", "names": ["POSTCARDIOTOMY SYNDROME", "Postcardiotomy syndrome", "postcardiotomy syndrome", "postcardiotomy; syndrome", "post cardiotomy syndrome", "POST CARDIOTOMY SYNDROME", "syndrome; postcardiotomy", "Postpericardiotomy syndrome", "postpericardiotomy syndrome", "Postpericardiotomy Syndrome", "POSTPERICARDIOTOMY SYNDROME", "post pericardiotomy syndrome", "Postpericardiotomy Syndromes", "Post-pericardiotomy syndrome", "POST PERICARDIOTOMY SYNDROME", "post-pericardiotomy syndrome", "Syndrome, Postpericardiotomy", "Post-Pericardiotomy Syndrome", "pericardiotomy post syndrome", "Syndromes, Postpericardiotomy", "Postcardiotomy syndrome (disorder)", "postcardiotomy syndrome (diagnosis)", "Post-pericardiotomy syndrome (disorder)", "Postcardiotomy syndrome - postoperative"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postpericardiotomy Syndrome", "shortest_name_length": 23}
{"curie": "UMLS:C0854965", "names": ["Stage I Penile Cancer", "stage I penile cancer", "penis cancer, stage I", "penile cancer, stage I", "Penis carcinoma stage I", "Stage I Carcinoma of Penis", "Stage I Penile Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Carcinoma of Penis", "shortest_name_length": 21}
{"curie": "UMLS:C3697597", "names": ["Non-specific intraventricular conduction delay", "Non-specific intraventricular conduction defect", "Nonspecific intraventricular conduction disorder", "Non-specific intraventricular conduction delay (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-specific intraventricular conduction delay", "shortest_name_length": 46}
{"curie": "UMLS:C3272812", "names": ["Colorectal Cribriform Comedo-Type Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Cribriform Comedo-Type Adenocarcinoma", "shortest_name_length": 48}
{"curie": "MONDO:0021258", "names": ["choroid tumor", "Choroid Tumor", "choroidal tumor", "Choroidal Tumor", "Choroid Neoplasm", "choroid neoplasm", "tumor of choroid", "Tumor of Choroid", "choroidal neoplasm", "Choroidal Neoplasm", "neoplasm of choroid", "Neoplasm of Choroid", "optic choroid tumor", "tumor of the choroid", "Tumor of the Choroid", "tumor of optic choroid", "optic choroid neoplasm", "neoplasm of the choroid", "Neoplasm of the Choroid", "neoplasm of optic choroid", "optic choroid neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choroid neoplasm", "shortest_name_length": 13}
{"curie": "MONDO:0015194", "names": ["ANEMIA SIDEROBLASTIC", "Sideroblastic anemia", "sideroblastic anemia", "Anemia sideroblastic", "Sideroblastic Anemia", "anemia sideroblastic", "Sideroblastic Anemias", "sideroblastic anaemia", "sideroblastic anemias", "Sideroblastic anaemia", "Anaemia sideroblastic", "sideroblastic; anemia", "Hypersideremic anemia", "Anemia, Sideroblastic", "anemia; sideroblastic", "ANAEMIA SIDEROBLASTIC", "Anemia, sideroblastic", "Sideroachrestic anemia", "Hypersideremic anaemia", "sideroachrestic anemia", "Anemias, Sideroblastic", "Sideroachrestic anaemia", "Anemia, sideroachrestic", "Sideroblastic anemia NOS", "Sideroblastic anemia, NOS", "Sideroblastic anaemia NOS", "Sideroblastic anaemia, NOS", "Sideroachrestic anemia, NOS", "Primary sideroblastic anemia", "Sideroachrestic anaemia, NOS", "primary sideroblastic anemia", "Anemia, primary sideroblastic", "Primary sideroblastic anaemia", "Sideroblastic anemia (disorder)", "sideroblastic anemia (diagnosis)", "Primary sideroblastic anemia, NOS", "anemia; refractory, sideroblastic", "sideroachrestic anemia (diagnosis)", "Primary sideroblastic anaemia, NOS", "Refractory sideroblastic anemia, NOS", "Refractory sideroblastic anaemia, NOS", "Anemia, hypochromic with iron loading", "anemia, hypochromic with iron loading", "primary sideroblastic anemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sideroblastic anemia", "shortest_name_length": 20}
{"curie": "UMLS:C5446576", "names": ["Conjunctival Leiomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conjunctival Leiomyosarcoma", "shortest_name_length": 27}
{"curie": "MONDO:0010868", "names": ["RMD1", "rippling muscle disease 1", "RIPPLING MUSCLE DISEASE 1", "Rippling Muscle Disease 1", "rippling muscle disease-1", "Rippling muscle disease, 1", "rippling muscle disease, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rippling muscle disease 1", "shortest_name_length": 4}
{"curie": "MONDO:0001387", "names": ["penis sarcoma", "PENIS, SARCOMA", "Penile Sarcoma", "penile sarcoma", "Sarcoma of Penis", "sarcoma of penis", "Sarcoma of the Penis", "sarcoma of the penis", "PENILE CANCER, SARCOMA", "sarcoma of penis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "penile sarcoma", "shortest_name_length": 13}
{"curie": "UMLS:C4727079", "names": ["Advanced Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Sarcoma", "shortest_name_length": 16}
{"curie": "UMLS:C2109263", "names": ["Oral Cavity Kaposi Sarcoma", "Kaposi's sarcoma of oral cavity", "Kaposi's sarcoma of oral cavity (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kaposi's sarcoma of oral cavity", "shortest_name_length": 26}
{"curie": "MONDO:0100163", "names": ["PMIS", "PIMS", "MISC", "MIS-C", "PIMS-TS", "MISC associated with COVID-19", "MIS-C associated with COVID-19", "COVID-19 Kawasaki-like syndrome", "SARS-CoV-2 Kawasaki-like syndrome", "Pediatric Multisystem Inflammatory Syndrome", "pediatric multisystem inflammatory syndrome", "Pediatric multisystem inflammatory syndrome", "Pediatric Inflammatory Multisystem Syndrome", "pediatric inflammatory multisystem syndrome", "Paediatric multisystem inflammatory syndrome", "Multisystem Inflammatory Syndrome in Children", "Multisystem inflammatory syndrome in children", "multisystem inflammatory syndrome in children", "Multi-system inflammatory syndrome in children", "paediatric inflammatory multisystemic syndrome", "PIMS - pediatric inflammatory multisystem syndrome", "PIMS - paediatric inflammatory multisystem syndrome", "MIS-C - multisystem inflammatory syndrome in children", "Multisystem inflammatory syndrome in children (disorder)", "COVID-19-Related Pediatric Inflammatory Multisystem Syndrome", "pediatric multisystem inflammatory disease, COVID-19 related", "pediatric multi-system inflammatory disease, COVID-19 related", "COVID-19 -related pediatric inflammatory multisystem syndrome", "pediatric multisystem inflammatory syndrome, COVID-19 related", "multisystem inflammatory disorder in children and adolescents", "multisystem inflammatory disease, pediatric, COVID-19 related", "multi-system inflammatory disease, pediatric, COVID-19 related", "multisystem inflammatory syndrome, pediatric, COVID-19 related", "pediatric multi-system inflammatory syndrome, COVID-19 related", "pediatric multisystem inflammatory syndrome, SARS-CoV-2 related", "multi-system inflammatory syndrome, pediatric, COVID-19 related", "pediatric multi-system inflammatory syndrome, SARS-CoV-2 related", "COVID-19–associated multisystem inflammatory syndrome in children", "COVID-19 associated multisystem inflammatory syndrome in children", "multisystem inflammatory syndrome in children with COVID-19 infection", "Multisystem Inflammatory Syndrome in Children Associated with COVID-19", "multisystem inflammatory syndrome in children associated with COVID-19", "multisystem inflammatory syndrome in children MIS-C associated with COVID-19", "multisystem inflammatory syndrome in children with COVID-19 infection (diagnosis)", "pediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2", "pediatric multi-system inflammatory syndrome potentially associated with COVID-19", "Pediatric Multi-System Inflammatory Syndrome Potentially Associated with COVID-19", "paediatric inflammatory multisystem syndrome: temporally associated with SARS-CoV-2", "multisystem inflammatory syndrome in children associated with coronavirus disease 2019", "PIMS-TS - pediatric inflammatory multisystem syndrome temporally associated with COVID-19", "PIMS-TS - paediatric inflammatory multisystem syndrome temporally associated with COVID-19"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "COVID-19–associated multisystem inflammatory syndrome in children", "shortest_name_length": 4}
{"curie": "UMLS:C0334242", "names": ["Papillary carcinoma in situ", "papillary carcinoma in situ", "Papillary Carcinoma In Situ", "Papillary carcinoma in-situ", "papillary carcinoma in situ (diagnosis)", "Papillary carcinoma in situ (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Papillary carcinoma in situ", "shortest_name_length": 27}
{"curie": "MONDO:0019456", "names": ["AML with multilineage dysplasia", "AML with Multilineage Dysplasia", "AML with myelodysplasia-related features", "Acute myeloid leukemia with multilineage dysplasia", "acute myeloid leukemia with multilineage dysplasia", "Acute Myeloid Leukemia with Multilineage Dysplasia", "Acute myeloid leukaemia with multilineage dysplasia", "acute myelogenous leukemia with multilineage dysplasia", "Acute myeloid leukemia with multilineage dysplasia NOS", "De novo acute myeloid leukemia with multilineage dysplasia", "Acute myeloid leukemia with prior myelodysplastic syndrome", "De novo Acute Myeloid Leukemia with Multilineage Dysplasia", "Acute myeloid leukaemia with prior myelodysplastic syndrome", "acute myelogenous leukemia (AML) with multilineage dysplasia", "Acute myeloid leukaemia with myelodysplasia-related features", "acute myeloid leukaemia with myelodysplasia-related features", "acute myelogenous leukemia with multilineage dysplasia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia with multilineage dysplasia", "shortest_name_length": 31}
{"curie": "UMLS:C1333450", "names": ["Esophageal High-Grade Dysplasia", "Esophageal High-Grade Intraepithelial Neoplasia", "Esophageal High Grade Intraepithelial Neoplasia", "Esophageal intraepithelial neoplasia, high grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal High Grade Intraepithelial Neoplasia", "shortest_name_length": 31}
{"curie": "MONDO:0003153", "names": ["brain stem glioma", "Brain Stem Glioma", "Adult Brainstem Glioma", "adult brainstem glioma", "Adult Brain Stem Glioma", "adult brain stem glioma", "brainstem glioma, adult", "glioma, adult brainstem", "glioma, adult brain stem", "brain stem glioma, adult", "glioma, brainstem, adult", "glioma, brain stem, adult", "Glioma of Adult Brain Stem", "glioma of adult brain stem", "brain stem glioma of adults", "glioma of the adult brain stem", "Glioma of the Adult Brain Stem", "adult brainstem neuroglial tumor", "adult Brainstem Neuroglial tumor", "Adult Brainstem Neuroglial Tumor", "adult CNS tumor, brainstem glioma", "CNS tumor, adult brainstem glioma", "CNS tumor, brainstem glioma, adult", "CNS tumor, adult brain stem glioma", "adult brain tumor, brainstem glioma", "Adult Brainstem Neuroglial Neoplasm", "CNS tumor, brain stem glioma, adult", "adult brainstem neuroglial neoplasm", "brain tumor, adult brainstem glioma", "adult brain tumor, brain stem glioma", "brain tumor, brainstem glioma, adult", "brain tumor, brain stem glioma, adult", "central nervous system tumor, brainstem glioma, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult brainstem glioma", "shortest_name_length": 17}
{"curie": "MONDO:0011435", "names": ["MCPH2", "Microcephaly, Primary Autosomal Recessive, 2", "MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE", "primary autosomal recessive microcephaly 2 with or without cortical malformations", "microcephaly 2, primary, autosomal recessive, with or without cortical malformations", "MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICAL MALFORMATIONS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly 2, primary, autosomal recessive, with or without cortical malformations", "shortest_name_length": 5}
{"curie": "MONDO:0006096", "names": ["atypical endometrial hyperplasia", "atypical hyperplasia endometrial", "Atypical Endometrial Hyperplasia", "Atypical endometrial hyperplasia", "Endometrial Hyperplasia, Atypical", "Atypical Endometrial Hyperplasias", "Hyperplasia, Atypical Endometrial", "Endometrial Hyperplasias, Atypical", "Hyperplasias, Atypical Endometrial", "atypical hyperplasia of endometrium", "Endometrial hyperplasia with atypia", "endometrial hyperplasia with atypia", "Atypical Hyperplasia of Endometrium", "Atypical hyperplasia of endometrium", "Endometrial Hyperplasia with Atypia", "Atypical Hyperplasia of the Endometrium", "atypical hyperplasia of the endometrium", "Atypical endometrial hyperplasia (disorder)", "atypical endometrial hyperplasia (diagnosis)", "endometrial hyperplasia with atypia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical endometrial hyperplasia", "shortest_name_length": 32}
{"curie": "MONDO:0020481", "names": ["MF", "myotonia fluctuans", "Myotonia fluctuans", "Myotonia Fluctuans", "MYOTONIA FLUCTUANS", "Fluctuating myotonia", "Myotonia fluctuans (disorder)", "Myotonia Fluctuans (disorder)", "myotonia fluctuans (diagnosis)", "Exercise-Induced Delayed-Onset Myotonia", "exercise-induced delayed-onset myotonia", "Exercise-induced delayed-onset myotonia", "Exercise induced delayed onset myotonia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myotonia fluctuans", "shortest_name_length": 2}
{"curie": "MONDO:0009567", "names": ["MSS", "Torsten Sjogren syndrome", "Marinesco-Sjogren syndrome", "Marinesco-Garland Syndrome", "Marinesco-Sjogren Syndrome", "Marinesco-Sjögren syndrome", "Marinesco Garland Syndrome", "Garland-Moorhouse syndrome", "Marinesco-Garland syndrome", "MARINESCO-SJOGREN SYNDROME", "Garland-Moorhouse Syndrome", "marinesco-sjogren syndrome", "Marinesco-Sjögren Syndrome", "marinesco sjogren syndrome", "Marinesco Sjogren Syndrome", "Garland Moorhouse Syndrome", "Marinesco Sjögren Syndrome", "Syndrome, Marinesco-Sjogren", "Syndrome, Marinesco-Garland", "Syndrome, Garland-Moorhouse", "Syndrome, Marinesco-Sjögren", "cataract-oligophrenia syndrome", "Marinesco-Sjogren syndrome (MSS)", "Marinesco Sjogren Garland Syndrome", "Marinesco-Sjogren-Garland Syndrome", "Marinesco-Sjogren-Garland syndrome", "Syndrome, Marinesco-Sjogren-Garland", "Marinesco Sjogren Syndrome Myopathy", "Marinesco-Sjogren Syndrome-Myopathy", "Marinesco-Sjogren syndrome-myopathy", "Syndrome-Myopathy, Marinesco-Sjogren", "Marinesco-Sjögren syndrome (disorder)", "Marinesco-Sjogren syndrome (diagnosis)", "oligophrenic cerebellolenticular degeneration", "Oligophrenic cerebellolenticular degeneration", "hereditary oligophrenic cerebellolental degeneration", "Hereditary Oligophrenic Cerebello-Lental Degeneration", "Hereditary Oligophrenic Cerebello Lental Degeneration", "hereditary oligophrenic cerebello-lental degeneration", "Marinesco Sjogren Syndrome Hypergonadotrophic Hypogonadism", "Marinesco-Sjogren Syndrome-Hypergonadotrophic Hypogonadism", "Marinesco-Sjogren syndrome-Hypergonadotrophic hypogonadism", "Syndrome-Hypergonadotrophic Hypogonadism, Marinesco-Sjogren", "Hypogonadism, Marinesco-Sjogren Syndrome-Hypergonadotrophic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Marinesco-Sjogren syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0014290", "names": ["NBIA6", "CoPAN", "COASY protein-associated neurodegeneration", "NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6", "neurodegeneration with brain iron accumulation 6", "COASY neurodegeneration with brain iron accumulation", "neurodegeneration with brain iron accumulation type 6", "Coenzyme A synthase protein associated neurodegeneration", "CoPAN - coenzyme A synthase protein associated neurodegeneration", "Coenzyme A synthase protein associated neurodegeneration (disorder)", "Neurodegeneration with brain iron accumulation due to COASY mutation", "neurodegeneration with brain iron accumulation due to COASY mutation", "neurodegeneration with brain iron accumulation caused by mutation in COASY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodegeneration with brain iron accumulation 6", "shortest_name_length": 5}
{"curie": "MONDO:0011863", "names": ["HPCQTL19", "HPCqtl19", "prostate cancer aggressiveness QTL", "prostate cancer aggressiveness quantitative trait locus on chromosome 19", "PROSTATE CANCER AGGRESSIVENESS QUANTITATIVE TRAIT LOCUS ON CHROMOSOME 19", "prostate cancer aggressiveness quantitative trait locus on chromosome type 19"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate cancer aggressiveness quantitative trait locus on chromosome 19", "shortest_name_length": 8}
{"curie": "UMLS:C0412842", "names": ["Poisoning by iron compound drug", "Iron and iron compound poisoning", "Poisoning by iron and its compounds", "Iron and/or iron compound poisoning", "Poisoning by iron and/or iron compound", "Poisoning by iron AND/OR its compounds", "Poisoning by iron and its compounds NOS", "Poisoning by iron and its compounds, NOS", "Poisoning caused by iron and/or iron compound", "Poisoning caused by iron and/or iron compound (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Poisoning by iron AND/OR its compounds", "shortest_name_length": 31}
{"curie": "MONDO:0014619", "names": ["TTD3", "TTDA", "photosensitive trichothiodystrophy 3", "Trichothiodystrophy 3, Photosensitive", "TRICHOTHIODYSTROPHY 3, PHOTOSENSITIVE", "trichothiodystrophy 3, photosensitive", "trichothiodystrophy complementation group A", "trichothiodystrophy, complementation group A", "TRICHOTHIODYSTROPHY, COMPLEMENTATION GROUP A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichothiodystrophy 3, photosensitive", "shortest_name_length": 4}
{"curie": "UMLS:C3273140", "names": ["Extrahepatic Bile Duct G3", "extrahepatic bile duct G3", "extrahepatic bile duct NEC", "Extrahepatic Bile Duct NEC", "Extrahepatic Bile Duct Neuroendocrine Carcinoma", "extrahepatic bile duct neuroendocrine carcinoma", "neuroendocrine carcinoma of the extrahepatic bile duct", "Extrahepatic Bile Duct High Grade Neuroendocrine Carcinoma", "extrahepatic bile duct high grade neuroendocrine carcinoma", "extrahepatic bile duct poorly differentiated endocrine carcinoma", "Extrahepatic Bile Duct Poorly Differentiated Endocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extrahepatic Bile Duct Neuroendocrine Carcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0006755", "names": ["euthyroid sick syndrome", "sick-euthyroid syndrome", "Euthyroid sick syndrome", "Euthyroid sick-syndrome", "sick euthyroid syndrome", "Sick euthyroid syndrome", "Sick-euthyroid syndrome", "Sick Euthyroid Syndrome", "SICK EUTHYROID SYNDROME", "Euthyroid Sick Syndrome", "Syndrome, Sick Euthyroid", "Euthyroid Sick Syndromes", "sick-euthyroid; syndrome", "syndrome; sick-euthyroid", "Non-Thyroidal Illness Syndrome", "Non Thyroidal Illness Syndrome", "Syndrome, Non-Thyroidal Illness", "Syndromes, Non-Thyroidal Illness", "Sick-euthyroid syndrome (disorder)", "euthyroid sick syndrome (diagnosis)", "EUTHYROID SICK SYNDROME LOW T3 LOW T4 SYNDROME", "EUTHYROID SICK SYNDROME <LOW T3/ LOW T4 SYNDROME>"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "euthyroid sick syndrome", "shortest_name_length": 23}
{"curie": "UMLS:C3640141", "names": ["Stage I Differentiated Thyroid Gland Cancer 45 Years and Older", "Stage I Differentiated Thyroid Gland Carcinoma 45 Years and Older", "Stage I Differentiated Thyroid Gland Carcinoma 45 Years and Older AJCC v7", "Stage I Thyroid Gland Papillary or Follicular Carcinoma 45 Years and Older"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Differentiated Thyroid Gland Carcinoma 45 Years and Older AJCC v7", "shortest_name_length": 62}
{"curie": "MONDO:0003273", "names": ["sternum cancer", "cancer of sternum", "neoplasm of sternum", "malignant sternal tumor", "Malignant Sternal Tumor", "malignant sternal neoplasm", "malignant tumor of sternum", "malignant sternum neoplasm", "Malignant Tumor of Sternum", "Malignant Sternal Neoplasm", "Malignant Neoplasm of Sternum", "malignant neoplasm of sternum", "Malignant Tumor of the Sternum", "malignant tumor of the sternum", "Malignant Neoplasm of the Sternum", "malignant neoplasm of the sternum", "bone neoplasm, malignant - sternum", "malignant neoplasm of sternum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sternum cancer", "shortest_name_length": 14}
{"curie": "UMLS:C1266019", "names": ["Sarcomatoid Hepatocellular Cancer", "Sarcomatous Hepatocellular Carcinoma", "Sarcomatoid Hepatocellular Carcinoma", "Hepatocellular carcinoma, sarcomatoid", "Hepatocellular carcinoma, spindle cell variant", "spindle cell hepatocellular carcinoma of liver", "spindle cell hepatocellular carcinoma of liver (diagnosis)", "Hepatocellular carcinoma, spindle cell variant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatocellular carcinoma, spindle cell variant", "shortest_name_length": 33}
{"curie": "UMLS:C4525588", "names": ["Stage IV Gastric Neuroendocrine Tumor", "Stage IV Gastric Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Gastric Neuroendocrine Tumor AJCC v8", "shortest_name_length": 37}
{"curie": "MONDO:0007129", "names": ["HYD1", "STHAG1", "MSX1 tooth agenesis", "Familial Tooth Agenesis", "Familial Tooth Ageneses", "Tooth Agenesis, Familial", "Ageneses, Familial Tooth", "Agenesis, Familial Tooth", "HYPODONTIA/OLIGODONTIA 1", "Tooth Ageneses, Familial", "TOOTH AGENESIS, FAMILIAL", "hypodontia/oligodontia 1", "tooth agenesis, familial", "Hypodontia Oligodontia 1", "Oligodontia 1, Hypodontia", "Hypodontia Oligodontia 1s", "Oligodontia 1s, Hypodontia", "Tooth Agenesis, Selective, 1", "TOOTH AGENESIS, SELECTIVE, 1", "tooth agenesis, selective, 1", "tooth agenesis, selective, type 1", "tooth agenesis caused by mutation in MSX1", "Hypodontia Oligodontia with Orofacial Cleft", "HYPODONTIA/OLIGODONTIA WITH OROFACIAL CLEFT", "hypodontia/oligodontia with orofacial cleft", "SECOND PREMOLARS AND THIRD MOLARS, ABSENCE OF", "second premolars and third molars, absence of", "tooth agenesis, selective, with orofacial cleft", "TOOTH AGENESIS, SELECTIVE, WITH OROFACIAL CLEFT", "Tooth Agenesis, Selective, With Orofacial Cleft", "tooth agenesis, selective, 1, with or without orofacial cleft"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tooth agenesis, selective, 1", "shortest_name_length": 4}
{"curie": "MONDO:0001252", "names": ["Plummer", "Toxic Goiter", "Toxic goiter", "PLUMMER DISEASE", "plummer disease", "Plummer disease", "disease plummers", "Plummer's disease", "plummer's disease", "Toxic struma nodosa", "Toxic nodular goitre", "Toxic Nodular Goiter", "Toxic nodular goiter", "toxic nodular goitre", "toxic nodular goiter", "goiter nodular toxic", "nodular; goiter, toxic", "struma; toxic, nodular", "GOITER, TOXIC, NODULAR", "struma; nodular, toxic", "toxic; goiter, nodular", "Toxic adenomatous goitre", "Toxic nodular goiter NOS", "Toxic adenomatous goiter", "Toxic nodular goiter, NOS", "Toxic nodular goitre, NOS", "adenomatous; goiter, toxic", "struma; toxic, adenomatous", "toxic; goiter, adenomatous", "goiter; adenomatous, toxic", "Toxic nodular goiter (disorder)", "Toxic nodular goiter, unspecified", "Toxic nodular goitre, unspecified", "Toxic nodular goiter, unspecified type", "Toxic nodular goitre, unspecified type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Plummer disease", "shortest_name_length": 7}
{"curie": "MONDO:0015679", "names": ["autosomal thrombocytopenia with normal platelets"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal thrombocytopenia with normal platelets", "shortest_name_length": 48}
{"curie": "MONDO:0002652", "names": ["Anal adenocarcinoma", "Anal Adenocarcinoma", "anal adenocarcinoma", "anus adenocarcinoma", "adenocarcinoma of anus", "Adenocarcinoma of Anus", "Adenocarcinoma of anus", "Adenocarcinoma of the Anus", "adenocarcinoma of the anus", "Adenocarcinoma of anus (disorder)", "adenocarcinoma of anus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anus adenocarcinoma", "shortest_name_length": 19}
{"curie": "UMLS:C3492932", "names": ["DLD Deficiency", "Maple Syrup Urine Disease, Type III", "Dihydrolipoamide Dehydrogenase Deficiency", "Lipoamide Dehydrogenase Deficiency, Lactic Acidosis due to", "Lactic Acidosis, Congenital Infantile, Due To LAD Deficiency", "Lactic Acidosis, Congenital Infantile, Due To Lad Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lactic Acidosis, Congenital Infantile, Due To Lad Deficiency", "shortest_name_length": 14}
{"curie": "MONDO:0019415", "names": ["NAIT", "NATP", "Neonatal Thrombocytopenia", "Neonatal Thrombocytopenias", "Thrombocytopenia, Neonatal", "Thrombocytopenias, Neonatal", "Neonatal isoimmune thrombocytopenia", "Isoimmune neonatal thrombocytopenia", "Alloimmune neonatal thrombocytopenia", "Neonatal alloimmune thrombocytopenia", "neonatal alloimmune thrombocytopenia", "Neonatal Alloimmune Thrombocytopenia", "Neonatal Alloimmune Thrombocytopenias", "Alloimmune Thrombocytopenia, Neonatal", "Thrombocytopenia, Neonatal Alloimmune", "Alloimmune Thrombocytopenias, Neonatal", "Thrombocytopenias, Neonatal Alloimmune", "INT - Isoimmune neonatal thrombocytopenia", "ANT - Alloimmune neonatal thrombocytopenia", "fetal and neonatal alloimmune thrombocytopenia", "neonatal alloimmune thrombocytopenia (diagnosis)", "Neonatal thrombocytopenia due to platelet alloimmunization", "Neonatal Thrombocytopenia due to Platelet Alloimmunization", "Neonatal thrombocytopenia due to platelet alloimmunisation", "Neonatal thrombocytopenia due to platelet alloimmunization (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fetal and neonatal alloimmune thrombocytopenia", "shortest_name_length": 4}
{"curie": "MONDO:0012437", "names": ["CCA4", "CTRCT21", "cataract 21 multiple types", "CATARACT 21, MULTIPLE TYPES", "cataract 21, multiple types", "congenital cataract cerulean type 4", "congenital cataract Cerulean type 4", "Cataract, Pulverulent, Juvenile-Onset", "cataract, pulverulent, juvenile-onset", "CATARACT, PULVERULENT, JUVENILE-ONSET", "Cataract, Congenital, Cerulean Type, 4", "MAF early-onset non-syndromic cataract", "CATARACT, CONGENITAL, CERULEAN TYPE, 4", "cataract, congenital, cerulean type, 4", "cataract 21 multiple types with or without microcornea", "CATARACT 21, MULTIPLE TYPES, WITH OR WITHOUT MICROCORNEA", "cataract 21, multiple types, with or without microcornea", "early-onset non-syndromic cataract caused by mutation in MAF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 21 multiple types", "shortest_name_length": 4}
{"curie": "UMLS:C4724972", "names": ["Recurrent Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Sarcoma", "shortest_name_length": 17}
{"curie": "UMLS:C4331325", "names": ["Stage II Oropharyngeal (p16-Negative) Throat Cancer", "Stage II Oropharyngeal (p16-Negative) Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Oropharyngeal (p16-Negative) Carcinoma AJCC v8", "shortest_name_length": 51}
{"curie": "UMLS:C3897952", "names": ["Perforating Open Globe Injury", "Perforating open globe injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perforating open globe injury", "shortest_name_length": 29}
{"curie": "UMLS:C4055189", "names": ["Treponema Pallidum Associated Congenital Nephrotic Syndrome", "Congenital Nephrotic Syndrome - Treponema Pallidum Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Nephrotic Syndrome - Treponema Pallidum Associated", "shortest_name_length": 59}
{"curie": "UMLS:C1336097", "names": ["Stage 0 Seminoma", "Intratubular Seminoma", "Stage 0 Seminoma of Testis", "Stage 0 Testicular Seminoma", "Stage 0 Seminoma of the Testis", "Stage 0 Testicular Seminoma AJCC v6, v7, and v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intratubular Seminoma", "shortest_name_length": 16}
{"curie": "MONDO:0003964", "names": ["FOP", "myositis ossifican", "Muscle ossification", "Myositis Ossificans", "ossificans myositis", "MYOSITIS OSSIFICANS", "Myositis ossificans", "myositis ossificans", "Myisitis ossificans", "ossification; muscle", "muscle; ossification", "ossificans; myositis", "myositis; ossificans", "muscle calcification", "Muscle calcification", "Muscular ossification", "Ossification - muscle", "ossification - muscle", "ossification of muscle", "muscular calcification", "Muscular ossification, NOS", "progressive ossifying myositis", "Ossifying interstitial myositis", "progressive myositis ossificans", "myositis ossificans progressiva", "Muscular ossification (disorder)", "ossification of muscle (diagnosis)", "fibrodysplasia ossificans progressiva", "Muscle calcification and ossification"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myositis ossificans", "shortest_name_length": 3}
{"curie": "UMLS:C0852711", "names": ["foot hand syndrome", "hand foot syndrome", "hand-foot syndrome", "Hand-and-foot syndrome", "Sickle Cell Dactylitis", "Sickle cell dactylitis", "Hand and foot syndrome", "Hand-foot syndrome in sickle cell anemia", "Hand-foot syndrome in sickle cell anaemia", "Hand-foot syndrome in sickle cell anemia (disorder)", "Hand and foot syndrome secondary to sickle cell anemia", "Hand and foot syndrome secondary to sickle cell anaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sickle Cell Dactylitis", "shortest_name_length": 18}
{"curie": "UMLS:C0866113", "names": ["Nephrotic syndrome with lesion of persistent glomerulonephritis", "Nephrotic Syndrome with Lesion of Persistent Glomerulonephritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome with Lesion of Persistent Glomerulonephritis", "shortest_name_length": 63}
{"curie": "UMLS:C1400310", "names": ["Iodine Deficiency Hypothyroidism", "hypothyroidism; iodine-deficiency", "iodine-deficiency; hypothyroidism", "Hypothyroidism due to Iodine Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Iodine Deficiency Hypothyroidism", "shortest_name_length": 32}
{"curie": "MONDO:0016004", "names": ["Aminopterin syndrome", "aminopterin syndrome", "Fetal aminopterin syndrome", "fetal aminopterin syndrome", "Foetal aminopterin syndrome", "fetal methotrexate syndrome", "Fetal methotrexate syndrome", "Fetal Methotrexate Syndrome", "Foetal methotrexate syndrome", "aminopterin fetopathy syndrome", "Aminopterin embryopathy syndrome", "aminopterin embryopathy syndrome", "Fetal aminopterin syndrome (disorder)", "Fetal aminopterin/methotrexate syndrome", "Foetal aminopterin/methotrexate syndrome", "aminopterin/methotrexate embryofetopathy", "Aminopterin/methotrexate embryofetopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aminopterin/methotrexate embryofetopathy", "shortest_name_length": 20}
{"curie": "MONDO:0016960", "names": ["partial trisomy of chromosome 9q", "partial duplication of chromosome 9q", "partial trisomy of the long arm of chromosome 9", "partial duplication of the long arm of chromosome 9", "partial trisomy of the long arm of chromosome type 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial trisomy of the long arm of chromosome 9", "shortest_name_length": 32}
{"curie": "MONDO:0016255", "names": ["body of uterus mixed neoplasm", "uterine corpus mixed epithelial and mesenchymal tumor", "Uterine Corpus Mixed Epithelial and Mesenchymal Tumor", "mixed epithelial and mesenchymal cancer of corpus uteri", "Uterine Corpus Mixed Epithelial and Mesenchymal Neoplasm", "uterine corpus mixed epithelial and mesenchymal neoplasm", "malignant mixed epithelial and mesenchymal tumor of corpus uteri"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine corpus mixed epithelial and mesenchymal neoplasm", "shortest_name_length": 29}
{"curie": "UMLS:C1378106", "names": ["stage I fallopian tube cancer", "Stage I Fallopian Tube Cancer", "Fallopian Tube Cancer Stage I", "fallopian tube cancer stage I", "AJCC stage I fallopian tube cancer", "AJCC Stage I Fallopian Tube Cancer", "Stage I Fallopian Tube Cancer AJCC v7", "Stage I Fallopian Tube Cancer AJCC v6", "FIGO stage I fallopian tube carcinoma", "stage I fallopian tube cancer AJCC v6", "FIGO Stage I Fallopian Tube Carcinoma", "stage I fallopian tube cancer AJCC v7", "FIGO stage I carcinoma of fallopian tube", "FIGO Stage I Carcinoma of Fallopian Tube", "FIGO Stage I Carcinoma of the Fallopian Tube", "FIGO stage I carcinoma of the fallopian tube", "Stage I Fallopian Tube Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Fallopian Tube Cancer", "shortest_name_length": 29}
{"curie": "UMLS:C0153257", "names": ["fever valley", "desert fever", "valley fever", "san joaquin fever", "Desert rheumatism", "desert rheumatism", "San Joaquin Valley fever", "Coccidioidal pneumonitis", "san joaquin valley fever", "fever joaquin san valley", "Primary coccidioidomycosis", "primary coccidioidomycosis", "Pulmonary coccidioidomycosis", "pulmonary coccidioidomycosis", "coccidioidomycosis pulmonary", "Coccidioidomycotic pneumonitis", "primary pulmonary coccidioidomycosis", "COCCIDIOIDOMYCOSIS PRIMARY PULMONARY", "Primary pulmonary coccidioidomycosis", "primary coccidioidomycosis (diagnosis)", "Primary coccidioidomycosis (pulmonary)", "Pulmonary coccidioidomycosis (disorder)", "Pulmonary coccidioidomycosis (diagnosis)", "Primary pulmonary coccidioidomycosis (disorder)", "primary pulmonary coccidioidomycosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary pulmonary coccidioidomycosis", "shortest_name_length": 12}
{"curie": "UMLS:C0332424", "names": ["Stage I Lymphoma", "Lymphoma stage I", "Lymphoma Stage I", "Ann Arbor Stage I Lymphoma", "Lymphoma stage I (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoma stage I", "shortest_name_length": 16}
{"curie": "UMLS:C5669726", "names": ["Extramedullary Disease in Multiple Myeloma Involving the Liver", "Extramedullary Disease in Plasma Cell Myeloma Involving the Liver"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extramedullary Disease in Plasma Cell Myeloma Involving the Liver", "shortest_name_length": 62}
{"curie": "UMLS:C1711192", "names": ["Sporadic Gastric Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sporadic Gastric Adenocarcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0013039", "names": ["3M2", "3M syndrome 2", "3M SYNDROME 2", "3-M syndrome 2", "three M syndrome 2", "THREE M SYNDROME 2", "Three M Syndrome 2", "OBSL1 3-M syndrome", "three M syndrome type 2", "3-M syndrome caused by mutation in OBSL1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "3M syndrome 2", "shortest_name_length": 3}
{"curie": "UMLS:C2981628", "names": ["Stage IVB Intrahepatic Cholangiocarcinoma", "Stage IVB Intrahepatic Cholangiocarcinoma AJCC v7", "Stage IVB Intrahepatic Bile Duct Cancer (Cholangiocarcinoma)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Intrahepatic Cholangiocarcinoma AJCC v7", "shortest_name_length": 41}
{"curie": "MONDO:0015210", "names": ["syndromic gastroduodenal malformation", "syndrome associated with gastroduodenal malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic gastroduodenal malformation", "shortest_name_length": 37}
{"curie": "MONDO:0004878", "names": ["female breast upper-outer quadrant cancer", "malignant tumor of upper outer quadrant of female breast", "malignant neoplasm of upper outer quadrant of female breast", "Malignant neoplasm of upper-outer quadrant of female breast", "Malignant neoplasm of upper-outer quadrant of breast, female", "Malignant neoplasm of upper-outer quadrant of female breast (disorder)", "malignant neoplasm of upper outer quadrant of female breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "female breast upper-outer quadrant cancer", "shortest_name_length": 41}
{"curie": "MONDO:0033947", "names": ["hereditary angioedema with normal C1Inh"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary angioedema with normal C1Inh", "shortest_name_length": 39}
{"curie": "MONDO:0011966", "names": ["ARPHM", "PVNH2", "PERIVENTRICULAR NODULAR HETEROTOPIA 2", "periventricular nodular heterotopia 2", "Periventricular Nodular Heterotopia 2", "HETEROTOPIA, PERIVENTRICULAR, AUTOSOMAL RECESSIVE", "Heterotopia, Periventricular, Autosomal Recessive", "heterotopia, periventricular, autosomal recessive", "Periventricular Heterotopia with Microcephaly, Autosomal Recessive", "periventricular heterotopia with microcephaly, autosomal recessive", "PERIVENTRICULAR HETEROTOPIA WITH MICROCEPHALY, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "periventricular heterotopia with microcephaly, autosomal recessive", "shortest_name_length": 5}
{"curie": "EFO:0010822", "names": ["stenosing tenosynovitis\"@e"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stenosing tenosynovitis\"@e", "shortest_name_length": 26}
{"curie": "MONDO:0014461", "names": ["HH22", "FEZF1 hypogonadotropic hypogonadism", "hypogonadotropic hypogonadism 22 with or without anosmia", "HYPOGONADOTROPIC HYPOGONADISM 22 WITH OR WITHOUT ANOSMIA", "hypogonadotropic hypogonadism 22, with or without anosmia", "hypogonadotropic hypogonadism caused by mutation in FEZF1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadotropic hypogonadism 22 with or without anosmia", "shortest_name_length": 4}
{"curie": "UMLS:C4727383", "names": ["Recurrent Chromophobe Renal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Chromophobe Renal Cell Carcinoma", "shortest_name_length": 42}
{"curie": "UMLS:C0266384", "names": ["Ametria", "ametria", "Uterus Absent", "uterus; aplasia", "aplasia; uterus", "agenesis uterus", "uterus; agenesis", "Uterine Agenesis", "uterine agenesis", "agenesis; uterus", "Uterine agenesis", "Aplasia of uterus", "Absence of Uterus", "Agenesis of uterus", "Aplasia of uterus NOS", "UTERUS CONGENITAL ABSENCE", "absence congenital uterus", "absence; uterus, congenital", "uterus; absence, congenital", "Congenital aplasia of uterus", "congenital aplasia of uterus", "congenital absence of uterus", "uterine agenesis (diagnosis)", "Congenital absence of uterus", "Agenesis of uterus (disorder)", "Congenital absence of uterus (disorder)", "congenital aplasia of uterus (diagnosis)", "anomalies of genital organs aplasia (congenital) uterus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital absence of uterus", "shortest_name_length": 7}
{"curie": "UMLS:C5243857", "names": ["Chronic graft versus host disease in eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic graft versus host disease in eye", "shortest_name_length": 40}
{"curie": "UMLS:C0877214", "names": ["Intestinal villi atrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal villi atrophy", "shortest_name_length": 24}
{"curie": "MONDO:0011926", "names": ["PSORS9", "psoriasis 9", "psoriasis susceptibility 9", "PSORIASIS SUSCEPTIBILITY 9", "psoriasis 9, susceptibility to", "PSORIASIS 9, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "psoriasis 9, susceptibility to", "shortest_name_length": 6}
{"curie": "MONDO:0008364", "names": ["Raynaud", "raynaud", "Raynauds", "raynauds", "raynaud phen", "phen raynauds", "raynauds' phen", "disease raynaud", "raynaud disease", "Raynaud disease", "Raynaud Disease", "RAYNAUD DISEASE", "Disease;Raynauds", "raynauds disease", "Raynaud syndrome", "Raynauds Disease", "Raynaud Syndrome", "disease raynauds", "raynaud syndrome", "RAYNAUDS DISEASE", "syndrome raynaud", "Raynauds disease", "disease raynaud's", "RAYNAUDS SYNDROME", "raynauds syndrome", "raynaud's disease", "Raynaud's disease", "raynaud s disease", "Raynaud's Disease", "Raynaud Phenomenon", "Raynaud phenomenon", "raynaud's syndrome", "RAYNAUD PHENOMENON", "Raynaud's Syndrome", "Raynaud's syndrome", "raynaud phenomenon", "Raynaud; phenomenon", "raynauds's syndrome", "Raynauds Phenomenon", "phenomenon; Raynaud", "phenomenon raynauds", "Raynauds phenomenon", "raynauds phenomenon", "phenomenon raynaud's", "raynaud's phenomenon", "Raynaud's Phenomenon", "Raynaud's phenomenon", "RAYNAUD'S PHENOMENON", "Cold Fingers, Hereditary", "COLD FINGERS, HEREDITARY", "cold fingers, hereditary", "Secondary Raynaud Disease", "secondary Raynaud disease", "Paroxysmal digital cyanosis", "Secondary Raynaud's Disease", "secondary Raynaud's disease", "cyanosis; paroxysmal digital", "Raynaud's disease (disorder)", "secondary Raynaud phenomenon", "Secondary Raynaud Phenomenon", "Secondary Raynaud phenomenon", "paroxysmal; digital cyanosis", "secondary Raynaud's phenomenon", "Secondary Raynaud's Phenomenon", "Raynaud's syndrome (diagnosis)", "Secondary Raynaud's phenomenon", "Raynaud's phenomenon (finding)", "Raynaud's phenomenon, secondary", "Raynaud's phenomenon (diagnosis)", "Raynaud's phenomenon (secondary)", "Raynaud's phenomenon (physical finding)", "Secondary Raynaud's phenomenon (finding)", "Raynaud's syndrome (disorder) [ambiguous]", "Raynaud's phenomenon (by history or observed)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Raynaud disease", "shortest_name_length": 7}
{"curie": "MONDO:0035375", "names": ["MIS-C/A", "multisystem inflammatory syndrome in children and adults"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multisystem inflammatory syndrome in children and adults", "shortest_name_length": 7}
{"curie": "UMLS:C4724971", "names": ["Refractory Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Sarcoma", "shortest_name_length": 18}
{"curie": "MONDO:0009273", "names": ["HYDM1", "hydatidiform mole", "Trophoblastic disease", "TROPHOBLASTIC DISEASE", "trophoblastic disease", "diseases trophoblastic", "trophoblastic; disorder", "Trophoblastic disease NOS", "Trophoblastic disease, NOS", "hydatidiform Mole, complete", "HYDATIDIFORM MOLE, RECURRENT, 1", "hydatidiform MOLE, recurrent, 1", "hydatidiform mole, recurrent, 1", "NLRP7 complete hydatidiform mole", "GESTATIONAL TROPHOBLASTIC DISEASE", "trophoblastic disease (diagnosis)", "Gestational trophoblastic disease", "gestational trophoblastic disease", "Gestational Trophoblastic Disease", "Gestational Trophoblastic Diseases", "Trophoblastic Disease, Gestational", "Gestational Trophoblastic Disorder", "Disease, Gestational Trophoblastic", "Trophoblastic Diseases, Gestational", "Diseases, Gestational Trophoblastic", "hydatidiform Mole, recurrent, type 1", "GTD - Gestational trophoblastic disease", "Gestational trophoblastic disease (disorder)", "complete hydatidiform mole caused by mutation in NLRP7", "Gestational trophoblastic disease (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hydatidiform mole, recurrent, 1", "shortest_name_length": 5}
{"curie": "UMLS:C5447314", "names": ["Invasive Female Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Invasive Female Breast Carcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C1321546", "names": ["Anaplastic Lymphoma", "Anaplastic Large B-Cell Lymphoma", "Anaplastic large B-cell lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anaplastic large B-cell lymphoma", "shortest_name_length": 19}
{"curie": "UMLS:C1333838", "names": ["Grade 2 Invasive Breast Carcinoma", "Grade 2 Infiltrating Breast Carcinoma", "Moderately Favorable Infiltrating Breast Carcinoma", "Moderately Differentiated Invasive Breast Carcinoma", "Moderately Differentiated Infiltrating Breast Carcinoma", "Intermediate Combined Histologic Grade Infiltrating Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade 2 Invasive Breast Carcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C5239293", "names": ["GCR", "Generalized Cutaneous Reticulohistiocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Generalized Cutaneous Reticulohistiocytosis", "shortest_name_length": 3}
{"curie": "MONDO:0020275", "names": ["oculocutaneous or ocular albinism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculocutaneous or ocular albinism", "shortest_name_length": 33}
{"curie": "UMLS:C2931208", "names": ["Usher syndrome type 1D", "Usher syndrome, type 1D", "Usher syndrome type 1D (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Usher syndrome, type 1D", "shortest_name_length": 22}
{"curie": "MONDO:0013677", "names": ["EDMD7", "Ehlers-Danlos syndrome, classic-like, 1", "autosomal dominant Emery-Dreifuss muscular dystrophy 7", "Emery-Dreifuss muscular dystrophy 7, autosomal dominant", "EMERY-DREIFUSS MUSCULAR DYSTROPHY 7, AUTOSOMAL DOMINANT", "EMERY-Dreifuss muscular dystrophy 7, autosomal dominant", "TMEM43 autosomal dominant Emery-Dreifuss muscular dystrophy", "autosomal dominant Emery-Dreifuss muscular dystrophy caused by mutation in TMEM43"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Emery-Dreifuss muscular dystrophy 7, autosomal dominant", "shortest_name_length": 5}
{"curie": "UMLS:C4289816", "names": ["Cervical Carcinoid Tumor", "Cervical Neuroendocrine Tumor G1", "Cervical Low Grade Neuroendocrine Tumor, Grade 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Neuroendocrine Tumor G1", "shortest_name_length": 24}
{"curie": "MONDO:0021927", "names": ["Arthrogryposis epileptic seizures migrational brain disorder", "arthrogryposis epileptic seizures migrational brain disorder", "Arthrogryposis multiplex congenita with epileptic seizures and migrational brain disorder", "arthrogryposis multiplex congenita with epileptic seizures and migrational brain disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis epileptic seizures migrational brain disorder", "shortest_name_length": 60}
{"curie": "MONDO:0017383", "names": ["familial clubfoot due to PITX1 point mutation", "hereditary clubfoot due to PITX1 point mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial clubfoot due to PITX1 point mutation", "shortest_name_length": 45}
{"curie": "UMLS:C0677781", "names": ["Neurofibromatosis 1 and 2 (NF1 and NF2)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neurofibromatosis 1 and 2 (NF1 and NF2)", "shortest_name_length": 39}
{"curie": "UMLS:C0279964", "names": ["high-grade, stage I adult NHL", "adult NHL, stage I, high grade", "NHL, high grade, stage I adult", "Stage I High Grade Adult Non-Hodgkin's Lymphoma", "lymphoma, high grade, stage I adult non-Hodgkin's", "adult non-Hodgkin's lymphoma, high grade, stage I", "non-Hodgkin's lymphoma, high grade, stage I adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I High Grade Adult Non-Hodgkin's Lymphoma", "shortest_name_length": 29}
{"curie": "MONDO:0004877", "names": ["transient neonatal thrombocytopenia", "Transient Neonatal Thrombocytopenia", "Transient neonatal thrombocytopenia", "thrombocytopenia; transient neonatal", "transient; thrombocytopenia, neonatal", "neonatal; thrombocytopenia, transitory", "Transient neonatal thrombocytopenia, NOS", "Transient neonatal thrombocytopenia (disorder)", "thrombocytopenic; purpura, neonatal, transitory", "transient neonatal thrombocytopenia (diagnosis)", "purpura; thrombocytopenic, neonatal, transitory"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transient neonatal thrombocytopenia", "shortest_name_length": 35}
{"curie": "MONDO:0014538", "names": ["CFEOM5", "fibrosis of extraocular muscles, congenital, 5", "FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 5", "congenital fibrosis of the extraocular muscles 5", "COL25A1 congenital fibrosis of extraocular muscles", "fibrosis of extraocular muscles, congenital, type 5", "congenital fibrosis of extraocular muscles caused by mutation in COL25A1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibrosis of extraocular muscles, congenital, 5", "shortest_name_length": 6}
{"curie": "MONDO:0019267", "names": ["Mutase- methylmalonic acidemia", "Mutase- methylmalonic acidaemia", "partial deficiency of methylmalonyl-CoA mutase", "Partial deficiency of methylmalonyl-CoA mutase", "Partial deficiency of methylmalonyl-coenzyme A mutase", "Vitamin B12-unresponsive methylmalonic aciduria type mut-", "Vitamin B12-unresponsive methylmalonic acidemia type mut-", "vitamin B12-unresponsive methylmalonic aciduria type mut-", "vitamin B12-unresponsive methylmalonic acidemia type mut-", "Partial deficiency of methylmalonyl-coenzyme A mutase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitamin B12-unresponsive methylmalonic acidemia type mut-", "shortest_name_length": 30}
{"curie": "UMLS:C4682805", "names": ["Stage IIB Testicular Cancer", "Stage IIB Testicular Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Testicular Cancer AJCC v8", "shortest_name_length": 27}
{"curie": "MONDO:0016930", "names": ["partial trisomy/tetrasomy of chromosome 9", "partial trisomy/tetrasomy of chromosome type 9", "partial duplication/triplication of chromosome 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial trisomy/tetrasomy of chromosome 9", "shortest_name_length": 41}
{"curie": "MONDO:0001610", "names": ["Acute dacryocystitis", "acute dacryocystitis", "dacryocystitis, acute", "dacryocystitis - acute", "Dacryocystitis - acute", "Acute dacryocystitis (disorder)", "acute dacryocystitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute dacryocystitis", "shortest_name_length": 20}
{"curie": "MONDO:0024545", "names": ["MMD1", "Miyoshi myopathy", "Miyoshi myopathy 1", "DYSF Miyoshi myopathy", "Miyoshi muscular dystrophy 1", "MIYOSHI muscular dystrophy 1", "Miyoshi myopathy caused by mutation in DYSF", "muscular dystrophy, distal, late-onset, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Miyoshi muscular dystrophy 1", "shortest_name_length": 4}
{"curie": "MONDO:0031400", "names": ["Tessadori-Van-Haaften neurodevelopmental syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tessadori-Van-Haaften neurodevelopmental syndrome", "shortest_name_length": 49}
{"curie": "UMLS:C2987213", "names": ["Hemoglobin Trait"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemoglobin Trait", "shortest_name_length": 16}
{"curie": "UMLS:C0280389", "names": ["Stage II Epidermoid Carcinoma of Hypopharynx", "Stage II Hypopharyngeal Epidermoid Carcinoma", "hypopharynx squamous cell carcinoma, stage II", "Stage II Hypopharyngeal Squamous Cell Carcinoma", "Stage II Squamous Cell Carcinoma of Hypopharynx", "Hypopharyngeal squamous cell carcinoma stage II", "hypopharyngeal squamous cell carcinoma, stage II", "Stage II Epidermoid Carcinoma of the Hypopharynx", "epidermoid carcinoma of the hypopharynx, stage II", "Squamous cell carcinoma of the hypopharynx stage II", "stage II squamous cell carcinoma of the hypopharynx", "Stage II Hypopharyngeal Throat Squamous Cell Cancer", "Stage II Squamous Cell Carcinoma of the Hypopharynx", "squamous cell carcinoma of the hypopharynx, stage II", "Stage II Hypopharyngeal Squamous Cell Carcinoma AJCC v6", "Stage II Hypopharyngeal Squamous Cell Carcinoma AJCC v7", "Stage II Hypopharyngeal Squamous Cell Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypopharyngeal squamous cell carcinoma stage II", "shortest_name_length": 44}
{"curie": "MONDO:0007283", "names": ["CTRCT42", "CATARACT 42", "cataract 42", "cataract type 42", "CRYBA2 early-onset non-syndromic cataract", "early-onset non-syndromic cataract caused by mutation in CRYBA2", "A cataract that has_material_basis_in heterozygous mutation in the CRYBA2 gene on chromosome 2q35."], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 42", "shortest_name_length": 7}
{"curie": "MONDO:0006648", "names": ["Anterior Tibial Syndrome", "ANTERIOR TIBIAL SYNDROME", "Anterior tibial syndrome", "anterior tibial syndrome", "Syndrome, Anterior Tibial", "Anterior Tibial Syndromes", "Tibial Syndrome, Anterior", "Tibial Syndromes, Anterior", "Syndromes, Anterior Tibial", "anterior compartment syndrome", "compartment syndrome anterior", "Anterior Compartment Syndrome", "Syndrome, Anterior Compartment", "Anterior Compartment Syndromes", "Compartment Syndrome, Anterior", "Syndromes, Anterior Compartment", "Compartment Syndromes, Anterior", "Anterior tibial compartment syndrome", "compartment syndrome of anterior tibia", "anterior compartment of tibia syndrome", "compartment syndrome of anterior tibial", "ACS - Anterior tibial compartment syndrome", "compartment syndrome of anterior tibia (diagnosis)", "compartment syndrome of anterior tibial compartment", "Anterior tibial compartment syndrome due to traumatic injury", "ACS - anterior tibial compartment syndrome due to traumatic injury", "Anterior tibial compartment syndrome due to traumatic injury (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anterior compartment of tibia syndrome", "shortest_name_length": 24}
{"curie": "MONDO:0008249", "names": ["coccyx; sinus", "Pilonidal Cyst", "pilonidal cyst", "PILONIDAL CYST", "cyst pilonidal", "Pilonidal cyst", "Cyst;pilonidal", "pilonidal cysts", "CYST, PILONIDAL", "Cyst, Pilonidal", "Pilonidal sinus", "pilonidal sinus", "Pilonidal Cysts", "sinus pilonidal", "PILONIDAL SINUS", "Coccygeal sinus", "coccygeal sinus", "pilonidal; cyst", "Piliferous cyst", "Pilonidal Sinus", "cyst; pilonidal", "Sinus;pilondial", "Cysts, Pilonidal", "sinus; coccygeal", "pilonidal; sinus", "Sinus, Pilonidal", "Cyst - pilonidal", "Pilliferous cyst", "sinus; pilonidal", "Pilonidal fistula", "Coccygeal fistula", "Pilonidal cyst NOS", "Pilonidal cyst, NOS", "pilonidal sinus cyst", "pilonidal cyst sinus", "Pilonidal cyst and sinus", "Pilonidal cyst (disorder)", "pilonidal sinus (disease)", "pilonidal cyst (diagnosis)", "pilonidal sinus (diagnosis)", "pilonidal sinus/cyst (non-specific)", "Pilonidal cyst (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pilonidal sinus", "shortest_name_length": 13}
{"curie": "UMLS:C0021308", "names": ["Infarct", "INFARCT", "infarct", "Infarcts", "INFARCTS", "infarction", "Infarction", "Infarctions", "Infarct, NOS", "Infarction NOS", "Infarction, NOS", "INFARCT INFARCTION", "Infarct (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infarction", "shortest_name_length": 7}
{"curie": "MONDO:0800146", "names": ["agammaglobulinemia, autosomal recessive, due to BOB1 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "agammaglobulinemia, autosomal recessive, due to BOB1 deficiency", "shortest_name_length": 63}
{"curie": "MONDO:0012970", "names": ["MVCD6", "NEPHROPATHY, DIABETIC, SUSCEPTIBILITY TO", "nephropathy, diabetic, susceptibility to", "microvascular complications of diabetes 6", "SOD2 microvascular complications of diabetes, susceptibility", "microvascular complications of diabetes, susceptibility to, 6", "MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 6", "microvascular complications of diabetes, susceptibility to, type 6", "MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 6 (finding)", "microvascular complications of diabetes, susceptibility caused by mutation in SOD2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microvascular complications of diabetes, susceptibility to, 6", "shortest_name_length": 5}
{"curie": "MONDO:0009392", "names": ["High hyperopia", "HYPEROPIA, HIGH", "hyperopia, high", "Hyperopia, High", "High hypermetropia", "Severe farsightedness", "Severe long-sightedness", "High-grade hypermetropia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperopia, high", "shortest_name_length": 14}
{"curie": "UMLS:C0399495", "names": ["Epulis Fissuratum", "Epulis fissuratum", "Denture granuloma", "epulis fissuratum", "irritation fibroma", "Denture hyperplasia", "hyperplasia denture", "epulis (fissuratum)", "Denture-induced hyperplasia", "epulis fissuratum of gingiva", "Denture irritation hyperplasia", "Denture-Induced Fibrous Hyperplasia", "epulis fissuratum of gingiva (diagnosis)", "Inflammatory fibrous hyperplasia caused by denture", "Inflammatory fibroepithelial hyperplasia of oral mucous membrane caused by denture", "Inflammatory fibroepithelial hyperplasia of oral mucous membrane caused by denture (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Inflammatory fibroepithelial hyperplasia of oral mucous membrane caused by denture", "shortest_name_length": 17}
{"curie": "MONDO:0011424", "names": ["Carney Triad", "Carney triad", "CARNEY TRIAD", "Carney triad (disorder)", "GASTRIC LEIOMYOSARCOMA, PULMONARY CHONDROMA, AND EXTRAADRENAL PARAGANGLIOMA", "gastric leiomyosarcoma, pulmonary chondroma, and extraadrenal paraganglioma", "Gastric Leiomyosarcoma, Pulmonary Chondroma, and Extraadrenal Paraganglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carney triad", "shortest_name_length": 12}
{"curie": "MONDO:0014576", "names": ["LIPT1D", "lipoyltransferase 1 deficiency", "LIPOYLTRANSFERASE 1 DEFICIENCY", "lipoyl transferase 1 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lipoyl transferase 1 deficiency", "shortest_name_length": 6}
{"curie": "MONDO:0010921", "names": ["nasal dermoid cyst", "nasal dermoid sinus cyst", "dermoid cysts, familial frontonasal", "DERMOID CYSTS, FAMILIAL FRONTONASAL", "Dermoid Cysts, Familial Frontonasal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasal dermoid cyst", "shortest_name_length": 18}
{"curie": "UMLS:C4727705", "names": ["Refractory Cutaneous Melanoma", "Refractory Melanoma of the Skin", "Refractory Cutaneous (Skin) Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Cutaneous Melanoma", "shortest_name_length": 29}
{"curie": "MONDO:0001496", "names": ["male genital organ stricture", "Male genital organ stricture", "stricture of male genital organs", "Stricture of male genital organs", "Male genital organ stricture (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "male genital organ stricture", "shortest_name_length": 28}
{"curie": "MONDO:0100339", "names": ["FA", "FRDA", "family ataxia", "familial ataxia", "Familial ataxia", "Friedreich Ataxia", "FRIEDREICH ATAXIA", "friedreich ataxia", "ataxia friedreich", "Friedreich ataxia", "friedreichs ataxia", "Friedreich Disease", "Friedreich Ataxias", "ataxia; Friedreich", "Ataxia, Friedreich", "friedrich's ataxia", "friedreich disease", "Friedreich; ataxia", "Friedrich's ataxia", "ATAXIA, FRIEDREICH", "FRIEDREICHS ATAXIA", "ataxia friedrich's", "friedrick's ataxia", "Friedrick's Ataxia", "Friedreich's tabes", "Ataxias, Friedreich", "friedreich's ataxia", "Disease, Friedreich", "Friedreich's ataxia", "Friedreich's Ataxia", "Friedreich ataxia 1", "Friedreich's disease", "Friedreich's Disease", "friedreich's disease", "Ataxia, Friedreich's", "Disease, Friedreich's", "FA - Friedreich ataxia", "Hereditary spinal ataxia", "hereditary spinal ataxia", "Hereditary Spinal Ataxia", "Friedreich Familial Ataxia", "Friedreichs Familial Ataxia", "spinal sclerosis hereditary", "Hereditary Spinal Sclerosis", "Hereditary Spinal Scleroses", "Ataxia, Friedreich Familial", "Familial Ataxia, Friedreich", "hereditary spinal sclerosis", "Scleroses, Hereditary Spinal", "Sclerosis, Hereditary Spinal", "Friedreich's Familial Ataxia", "Spinal Sclerosis, Hereditary", "Friedreich Hereditary Ataxia", "Spinal Scleroses, Hereditary", "Friedreichs Hereditary Ataxia", "Familial Ataxia, Friedreich's", "Ataxia, Friedreich's Familial", "Ataxia, Friedreich Hereditary", "Hereditary Ataxia, Friedreich", "friedreich's hereditary ataxia", "Friedreich's Hereditary Ataxia", "Friedreich's ataxia (disorder)", "Friedreich's Hereditary Ataxias", "Ataxia, Friedreich's Hereditary", "Hereditary Ataxia, Friedreich's", "Friedreich's ataxia (diagnosis)", "Hereditary ataxia of Friedreich", "Hereditary Ataxias, Friedreich's", "Ataxias, Friedreich's Hereditary", "Friedreich Spinocerebellar Ataxia", "spinocerebellar ataxia, Friedreich", "Spinocerebellar Ataxia, Friedreich", "Ataxia, Friedreich Spinocerebellar", "Friedreich Hereditary Spinal Ataxia", "Hereditary Spinal Ataxia, Friedreich", "Friedreich; combined systemic disease", "Friedreich's Hereditary Spinal Ataxia", "combined; systemic disease, Friedreich", "hereditary; spinal ataxia (Friedreich)", "ataxia; spinal hereditary (Friedreich)", "Hereditary Spinal Ataxia, Friedreich's", "ataxia; hereditary, spinal (Friedreich)", "hereditary; ataxia, spinal (Friedreich)", "spinal; ataxia, hereditary (Friedreich)", "Friedreich ataxia with retained reflexes", "spinal; hereditary sclerosis (Friedreich's ataxia)", "hereditary; spinal sclerosis (Friedreich's ataxia)", "hereditary; sclerosis, spinal (Friedreich's ataxia)", "sclerosis; hereditary, spinal (Friedreich's ataxia)", "sclerosis; spinal, hereditary (Friedreich's ataxia)", "spinal; sclerosis, hereditary (Friedreich's ataxia)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Friedreich ataxia", "shortest_name_length": 2}
{"curie": "UMLS:C0238065", "names": ["Secondary biliary cirrhosis", "secondary biliary cirrhosis", "Biliary cirrhosis secondary", "Secondary Biliary Cirrhosis", "BILIARY CIRRHOSIS SECONDARY", "Obstructive Liver Cirrhosis", "CIRRHOSIS, SECONDARY BILIARY", "Cirrhosis, Secondary Biliary", "Biliary Cirrhosis, Secondary", "Liver Cirrhosis, Obstructive", "cirrhosis; biliary, secondary", "Secondary Biliary Cholangitis", "Cholangitis, Secondary Biliary", "Biliary Cholangitis, Secondary", "Secondary Biliary Cholangitides", "Secondary biliary cirrhosis (disorder)", "secondary biliary cirrhosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary Biliary Cholangitis", "shortest_name_length": 27}
{"curie": "UMLS:C1335346", "names": ["Parasite-Related Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parasite-Related Carcinoma", "shortest_name_length": 26}
{"curie": "UMLS:C1960221", "names": ["lymphoma in remission", "Lymphoma in Remission", "Lymphoma in remission", "Malignant lymphoma in remission", "lymphoma in remission (diagnosis)", "Malignant lymphoma in remission (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant lymphoma in remission", "shortest_name_length": 21}
{"curie": "MONDO:0001904", "names": ["Polyneuropathy due to drug", "polyneuropathy due to drug", "Polyneuropathy due to drugs", "drug-induced polyneuropathy", "Drug-related polyneuropathy", "Drug-induced polyneuropathy", "Polyneuropathy caused by drug", "Polyneuropathy due to drug, NOS", "drug-induced polyneuropathy (diagnosis)", "Polyneuropathy caused by drug (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyneuropathy due to drug", "shortest_name_length": 26}
{"curie": "UMLS:C3273227", "names": ["Bronchial Epithelial Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bronchial Epithelial Hyperplasia", "shortest_name_length": 32}
{"curie": "MONDO:0020667", "names": ["ABS2", "trapezoidocephaly-synostosis Syndrome", "osteodysgenesis, multisynostotic, with fractures", "multisynostotic osteodysgenesis with long bone fractures", "Antley-Bixler syndrome without disordered steroidogenesis", "Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis", "shortest_name_length": 4}
{"curie": "MONDO:0042979", "names": ["HOKPP", "HOKPP1", "HYPOKALEMIC PERIODIC PARALYSIS", "hypokalemic periodic paralysis type 1", "Hypokalemic periodic paralysis type 1", "HYPOKALEMIC PERIODIC PARALYSIS, TYPE 1", "hypokalemic periodic paralysis, type 1", "hypokalemic periodic paralysis type 1 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypokalemic periodic paralysis, type 1", "shortest_name_length": 5}
{"curie": "UMLS:C3273089", "names": ["juvenile rickets", "infantile rickets", "Childhood Rickets"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Rickets", "shortest_name_length": 16}
{"curie": "MONDO:0007711", "names": ["Bencze syndrome", "Bencze Syndrome", "BENCZE SYNDROME", "hemifacial hyperplasia strabismus", "Hemifacial Hyperplasia With Strabismus", "HEMIFACIAL HYPERPLASIA WITH STRABISMUS", "hemifacial hyperplasia with strabismus", "Hemifacial hyperplasia strabismus syndrome", "Hemifacial hyperplasia-strabismus syndrome", "hemifacial hyperplasia-strabismus syndrome", "Hemifacial hyperplasia strabismus syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bencze syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0010925", "names": ["VELOFACIOSKELETAL syndrome", "Velofacioskeletal syndrome", "VELOFACIOSKELETAL SYNDROME", "velo-facial-skeletal syndrome", "Velo-facial-skeletal syndrome", "Velofacioskeletal syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "velo-facial-skeletal syndrome", "shortest_name_length": 26}
{"curie": "UMLS:C1332051", "names": ["AIDS-related NHL", "AIDS-Related Non-Hodgkin Lymphoma", "AIDS-related Non-Hodgkin lymphoma", "AIDS-Related Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Non-Hodgkin Lymphoma", "shortest_name_length": 16}
{"curie": "MONDO:0015038", "names": ["lissencephaly with cerebellar hypoplasia type E"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lissencephaly with cerebellar hypoplasia type E", "shortest_name_length": 47}
{"curie": "UMLS:C0266008", "names": ["anomaly; breast", "breast; anomaly", "Breast anomalies", "malformation breast", "BREAST MALFORMATION", "Breast malformation", "anomalies of breast", "breast malformations", "CONGENITAL ANOMALY OF BREAST", "congenital anomaly of breast", "Congenital anomaly of breast", "deformity; breast, congenital", "breast; deformity, congenital", "anomalies of breast (diagnosis)", "Congenital anomaly of breast, NOS", "Congenital malformation of breast", "Congenital malformations of breast", "CONGENITAL ANOMALIES OF THE BREAST", "Congenital malformation of breast, NOS", "Congenital anomaly of breast (disorder)", "Congenital malformation of breast, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital anomaly of breast", "shortest_name_length": 15}
{"curie": "UMLS:C2987218", "names": ["Pancreatic Acinar Cell Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Acinar Cell Neoplasm", "shortest_name_length": 31}
{"curie": "MONDO:0009272", "names": ["GERMAN SYNDROME", "German syndrome", "German Syndrome", "German syndrome (disorder)", "Hypotonia-arthrogryposis-facial dysmorphism-lymphedema syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "German syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0016209", "names": ["benign nocturnal alternating hemiplegia of childhood", "benign familial nocturnal alternating hemiplegia in childhood", "benign familial nocturnal alternating hemiplegia of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign familial nocturnal alternating hemiplegia of childhood", "shortest_name_length": 52}
{"curie": "UMLS:C1456792", "names": ["Still disease", "Still's disease with juvenile onset and/or adult onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Still's disease with juvenile onset and/or adult onset", "shortest_name_length": 13}
{"curie": "MONDO:0004849", "names": ["emphysema", "Emphysema", "EMPHYSEMA", "Emphysemas", "Emphysema, NOS", "Emphysema/COPD", "lung emphysema", "Pneumonectasis", "Other emphysema", "Emphysema of lung", "Emphysema pulmonary", "pulmonary emphysema", "Pulmonary Emphysema", "PULMONARY EMPHYSEMA", "Pulmonary emphysema", "EMPHYSEMA PULMONARY", "Emphysema, Pulmonary", "Pulmonary Emphysemas", "emphysema, pulmonary", "PULMONARY EMPHYSEMAS", "EMPHYSEMA, PULMONARY", "Emphysemas, Pulmonary", "emphysema (diagnosis)", "Emphysema (Pulmonary)", "Emphysema, unspecified", "Emphysema of lung, NOS", "Pulmonary emphysema, NOS", "Pulmonary emphysema (disorder)", "Emphysema (lung)(pulmonary) NOS", "Emphysema (morphologic abnormality)", "abnormal collection of air in tissues", "Pathological accumulation of air in tissues"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary emphysema", "shortest_name_length": 9}
{"curie": "UMLS:C4725867", "names": ["Resectable Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Liposarcoma", "shortest_name_length": 22}
{"curie": "UMLS:C3641712", "names": ["ENSAT Stage IV Adrenal Cortex Cancer", "ENSAT Stage IV Adrenal Cortex Carcinoma", "ENSAT Stage IV Adrenal Cortical Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ENSAT Stage IV Adrenal Cortical Carcinoma", "shortest_name_length": 36}
{"curie": "MONDO:0011957", "names": ["MCDR2", "MACULAR DYSTROPHY, RETINAL, 2", "macular dystrophy, retinal, 2", "Macular Dystrophy, Retinal, 2", "Retinal macular dystrophy type 2", "retinal macular dystrophy type 2", "macular dystrophy, retinal, type 2", "MCDR2 - retinal macular dystrophy type 2", "Retinal macular dystrophy type 2 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal macular dystrophy type 2", "shortest_name_length": 5}
{"curie": "MONDO:0005333", "names": ["hyperthyroxinemia", "Hyperthyroxinemia", "Hyperthyroxinemias"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperthyroxinemia", "shortest_name_length": 17}
{"curie": "MONDO:0018998", "names": ["LCA", "leber's disease", "Leber's disease", "Leber amaurosis", "Leber disease 2", "Leber Amaurosis", "amaurosis; Leber", "Leber; amaurosis", "Leber Abiotrophy", "Lebers Amaurosis", "Leber abiotrophy", "leber's amaurosis", "Leber's Amauroses", "Abiotrophy, Leber", "Leber's amaurosis", "Leber's Amaurosis", "Leber Abiotrophies", "Amaurosis, Leber's", "Amauroses, Leber's", "Abiotrophies, Leber", "leber congenital amaurosis", "Leber congenital amaurosis", "hereditary retinal aplasia", "Leber Congenital Amauroses", "Leber Congenital Amaurosis", "amaurosis congenital lebers", "Amaurosis, Leber Congenital", "Amauroses, Leber Congenital", "Congenital Amauroses, Leber", "Congenital Amaurosis, Leber", "Leber; congenital amaurosis", "congenital amaurosis; Leber", "amaurosis congenita of Leber", "congenital; amaurosis, Leber", "leber's congenital amaurosis", "Amaurosis congenita of Leber", "Congenital retinal blindness", "congenital retinal blindness", "Leber's amaurosis (disorder)", "Leber's congenital amaurosis", "amaurosis leber's congenital", "Congenital Retinal Blindness", "Blindness, Congenital Retinal", "Congenital Retinal Blindnesses", "Blindnesses, Congenital Retinal", "congenital retinitis pigmentosa", "heredoretinopathia congenitalis", "Retinal Blindnesses, Congenital", "Leber congenital amaurosis (LCA)", "congenital retinal blindness (CRB)", "CRB - Congenital retinal blindness", "dysgenesis neuroepithelialis retinae", "congenital amaurosis of retinal origin", "Leber's congenital amaurosis (diagnosis)", "congenital absence of the rods and cones", "hereditary epithelial dysplasia of retina", "Leber's congenital tapetoretinal dysplasia", "Leber congenital tapetoretinal degeneration", "Leber Congenital Tapetoretinal Degeneration", "Leber's congenital tapetoretinal degeneration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leber congenital amaurosis", "shortest_name_length": 3}
{"curie": "MONDO:0011722", "names": ["MOMES Syndrome", "MOMES SYNDROME", "Momes syndrome", "MOMES syndrome", "Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome", "intellectual disability-obesity-prognathism-eye and skin anomalies syndrome", "intellectual disability, obesity, prognathism, eye and skin anomalies syndrome", "Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome", "Mental Retardation, Obesity, Mandibular Prognathism, and Eye and Skin Anomalies", "mental retardation, obesity, mandibular prognathism, and eye and skin anomalies", "MENTAL RETARDATION, OBESITY, MANDIBULAR PROGNATHISM, AND EYE AND SKIN ANOMALIES", "intellectual disability, obesity, mandibular prognathism, and eye and skin anomalies", "Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome (disorder)", "intellectual disability, obesity, prognathism, eye and skin anomalies syndrome (diagnosis)", "IMPAIRED INTELLECTUAL DEVELOPMENT, OBESITY, MANDIBULAR PROGNATHISM, AND EYE AND SKIN ANOMALIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability-obesity-prognathism-eye and skin anomalies syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0024479", "names": ["epithelial tumor of colon", "colon epithelial neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epithelial tumor of colon", "shortest_name_length": 25}
{"curie": "UMLS:C1334265", "names": ["Intrathoracic Paravertebral Paraganglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intrathoracic Paravertebral Paraganglioma", "shortest_name_length": 41}
{"curie": "UMLS:C0549398", "names": ["meibomitis", "MEIBOMITIS", "Meibomitis", "MEIBOMIANITIS", "Meibomianitis", "meibomianitis", "Meibomianitis (disorder)", "meibomianitis (diagnosis)", "meibomianitis was observed", "meibomianitis (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meibomianitis", "shortest_name_length": 10}
{"curie": "MONDO:0007311", "names": ["Cmt1e", "CMT1E", "CMT 1E", "Charcot Marie Tooth disease type 1E", "Charcot-Marie-Tooth disease type IE", "Charcot-Marie-Tooth disease type 1E", "Charcot-Marie-Tooth disease-deafness", "Charcot-Marie-Tooth disease, type 1E", "Charcot-Marie-Tooth disease, Type 1E", "Charcot-Marie-Tooth disease and deafness", "CHARCOT-MARIE-TOOTH DISEASE AND DEAFNESS", "Charcot-Marie-Tooth disease-deafness syndrome", "Charcot-Marie-Tooth disease type IE (disorder)", "Charcot-Marie-Tooth disease type 1E (diagnosis)", "Charcot-Marie-Tooth disease demyelinating type 1E", "Charcot-Marie-Tooth disease-hearing loss syndrome", "Charcot-Marie-Tooth disease, demyelinating, type 1E", "CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1E", "Charcot-Marie-Tooth Disease, Demyelinating, Type 1e", "autosomal dominant Charcot-Marie-Tooth neuropathy and deafness", "CHARCOT-MARIE-TOOTH NEUROPATHY AND DEAFNESS, AUTOSOMAL DOMINANT", "Charcot-Marie-Tooth Neuropathy And Deafness, Autosomal Dominant", "Charcot-Marie-Tooth neuropathy and deafness, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 1E", "shortest_name_length": 5}
{"curie": "UMLS:C0855143", "names": ["Stage II Nodal Marginal Zone Lymphoma", "Nodal Marginal Zone B-Cell Lymphoma Stage II", "Nodal marginal zone B-cell lymphoma stage II", "Stage II Nodal Marginal Zone B-Cell Lymphoma", "Ann Arbor Stage II Nodal Marginal Zone Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nodal marginal zone B-cell lymphoma stage II", "shortest_name_length": 37}
{"curie": "UMLS:C1504346", "names": ["Pruritus allergic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pruritus allergic", "shortest_name_length": 17}
{"curie": "MONDO:0016888", "names": ["partial deletion of chromosome 6p", "partial monosomy of chromosome 6p", "partial monosomy of the short arm of chromosome 6", "partial deletion of the short arm of chromosome 6", "partial deletion of the short arm of chromosome type 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of the short arm of chromosome 6", "shortest_name_length": 33}
{"curie": "MONDO:0014646", "names": ["ZLS2", "ZIMMERMANN-LABAND SYNDROME 2", "Zimmermann-Laband syndrome 2", "Zimmermann-Laband syndrome type 2", "ATP6V1B2 Zimmermann-Laband syndrome", "Zimmermann-Laband syndrome caused by mutation in ATP6V1B2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Zimmermann-Laband syndrome 2", "shortest_name_length": 4}
{"curie": "UMLS:C5557368", "names": ["Vulvar Lipoblastoma-Like Tumor", "Vulvar Lipoblastoma-Like Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Lipoblastoma-Like Tumor", "shortest_name_length": 30}
{"curie": "MONDO:0033639", "names": ["MC4DN10", "mitochondrial complex 4 deficiency, nuclear type 10", "mitochondrial complex IV deficiency, nuclear type 10", "MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 4 deficiency, nuclear type 10", "shortest_name_length": 7}
{"curie": "MONDO:0024416", "names": ["neorickettsiosis", "NEORICKETTSIOSES", "Neorickettsiosis", "Neorickettsiosis, NOS", "Neorickettsiosis (disorder)", "Neorickettsia infectious disease", "Neorickettsia disease or disorder", "Neorickettsia caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neorickettsia infectious disease", "shortest_name_length": 16}
{"curie": "MONDO:0700076", "names": ["GA2C", "ETFDH deficiency", "glutaric acidemia 2C", "glutaric acidemia IIc", "multiple acyl-CoA dehydrogenase deficiency caused by mutation in ETFDH"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glutaric acidemia IIc", "shortest_name_length": 4}
{"curie": "MONDO:0015026", "names": ["CRMCC2", "STN1 Coats plus syndrome", "Coats plus syndrome caused by mutation in STN1", "cerebroretinal microangiopathy with calcifications and cysts 2", "CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS 2", "cerebroretinal microangiopathy with calcifications and cysts type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebroretinal microangiopathy with calcifications and cysts 2", "shortest_name_length": 6}
{"curie": "MONDO:0006947", "names": ["Renovascular hypertension", "hypertension renovascular", "RENOVASCULAR HYPERTENSION", "Renovascular Hypertension", "renovascular hypertension", "renovascular; hypertension", "hypertension; renovascular", "Hypertension, Renovascular", "renovascular hypertension (disease)", "secondary hypertension renovascular", "hypertension; renovascular disorders", "Renovascular hypertension (disorder)", "renovascular hypertension (diagnosis)", "renal disease; hypertension, arterial", "Hypertension due to renovascular disease", "Hypertension due to renal artery hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renovascular hypertension", "shortest_name_length": 25}
{"curie": "MONDO:0004510", "names": ["Inflammatory ALT/WDLPS", "inflammatory liposarcoma", "Inflammatory Liposarcoma", "Inflammatory liposarcoma", "Inflammatory Atypical Lipomatous Tumor/Well-Differentiated Liposarcoma", "Inflammatory Atypical Lipomatous Tumor/Well Differentiated Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory liposarcoma", "shortest_name_length": 22}
{"curie": "UMLS:C0340445", "names": ["Bacterial pericarditis", "Bacterial Pericarditis", "bacterial pericarditis", "pericarditis; bacterial", "bacterial; pericarditis", "Bacterial pericarditis (disorder)", "bacterial pericarditis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bacterial pericarditis", "shortest_name_length": 22}
{"curie": "MONDO:0007145", "names": ["ACC", "cuti aplasia", "Cutis aplasia", "cutis aplasia", "skin; aplasia", "Aplasia cutis", "aplasia cutis", "aplasia; skin", "Congenital scar", "Aplasia of skin", "congenital scar", "Congenital scars", "congenita aplasia cuti", "aplasia congenita cutis", "scalp defect congenital", "Aplasia cutis congenita", "aplasia cutis congenita", "Aplasia Cutis Congenita", "aplasia; cutis congenita", "scalp defect, congenital", "SCALP DEFECT, CONGENITAL", "cutis congenita; aplasia", "Scalp defect, congenital", "Congenital absence of skin", "Aplasia of skin (disorder)", "Congenital scar (disorder)", "Aplasia cutis of the scalp", "congenital scar (diagnosis)", "Epitheliogenesis imperfecta", "ACC - Aplasia cutis congenita", "Absence of part of skin at birth", "aplasia cutis congenita (disease)", "aplasia cutis congenita recessive", "Aplasia cutis congenita (disorder)", "aplasia cutis congenita (diagnosis)", "Congenital defect of skull and scalp", "CONGENITAL DEFECT OF SKULL AND SCALP", "congenital defect of skull and scalp", "aplasia cutis congenita nonsyndromic", "nonsyndromic aplasia cutis congenita", "APLASIA CUTIS CONGENITA, NONSYNDROMIC", "aplasia cutis congenita, nonsyndromic", "Aplasia Cutis Congenita, Nonsyndromic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aplasia cutis congenita", "shortest_name_length": 3}
{"curie": "MONDO:0014291", "names": ["DFNA54", "autosomal dominant deafness 54", "DEAFNESS, AUTOSOMAL DOMINANT 54", "deafness, autosomal dominant 54", "autosomal dominant nonsyndromic deafness 54", "autosomal dominant nonsyndromic hearing loss 54", "autosomal dominant nonsyndromic deafness type 54"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 54", "shortest_name_length": 6}
{"curie": "MONDO:0005856", "names": ["Mononegavirales Infection", "Mononegavirales Infections", "Infection, Mononegavirales", "Infections, Mononegavirales", "Mononegavirales infectious disease", "Mononegavirales disease or disorder", "Mononegavirales caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mononegavirales infectious disease", "shortest_name_length": 25}
{"curie": "UMLS:C4682624", "names": ["Stage IIIA1 Ovarian Cancer", "Stage IIIA1 Ovarian Cancer AJCC v8", "Stage IIIA1 Ovarian Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA1 Ovarian Cancer AJCC v8", "shortest_name_length": 26}
{"curie": "UMLS:C0267581", "names": ["rectal stenosis", "Rectal stenosis", "rectum stenosis", "Rectal Stenosis", "rectum; stenosis", "stenosis; rectum", "Stenosis of rectum", "stenosis of rectum", "Stenosis of rectum (disorder)", "stenosis of rectum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rectal Stenosis", "shortest_name_length": 15}
{"curie": "MONDO:0004996", "names": ["Childhood AML", "childhood AML", "pediatric AML", "aml childhood", "Pediatric AML", "pediatric AGL", "aml pediatric", "AML, pediatric", "AML, childhood", "AGL, childhood", "AGL, pediatric", "acute myeloid leukemia (AML)", "Acute Myeloid Leukemia (AML)", "Childhood Acute Myeloid Leukemia", "pediatric acute myeloid leukemia", "Pediatric Acute Myeloid Leukemia", "childhood acute myeloid leukemia", "leukemia, childhood acute myeloid", "childhood acute myeloid leukaemia", "childhood leukemia, acute myeloid", "acute myeloid leukemia, childhood", "acute myeloid leukemia, pediatric", "myeloid leukemia, childhood acute", "pediatric leukemia, acute myeloid", "leukemia, pediatric acute myeloid", "myeloid leukemia, pediatric acute", "paediatric acute myeloid leukaemia", "acute myeloid leukemia of childhood", "childhood acute myelocytic leukemia", "pediatric acute myelocytic leukemia", "Leukemia, acute myeloid (AML), child", "pediatric acute myelogenous leukemia", "myelocytic leukemia, childhood acute", "childhood acute myelogenous leukemia", "Childhood Acute Myelogenous Leukemia", "acute myelocytic leukemia, childhood", "Pediatric Acute Myelogenous Leukemia", "Childhood Acute Myeloblastic Leukemia", "leukemia, pediatric acute myelogenous", "childhood acute granulocytic leukemia", "childhood leukemia, acute myelogenous", "myelogenous leukemia, childhood acute", "Pediatric Acute Myeloblastic Leukemia", "pediatric leukemia, acute myelogenous", "leukemia, childhood acute myelogenous", "myelogenous leukemia, pediatric acute", "childhood acute myeloblastic leukemia", "acute myelogenous leukemia, pediatric", "pediatric acute myeloblastic leukemia", "pediatric acute granulocytic leukemia", "acute myelogenous leukemia, childhood", "myeloblastic leukemia, childhood acute", "granulocytic leukemia, childhood acute", "leukemia, childhood acute myeloblastic", "acute myeloblastic leukemia, childhood", "acute granulocytic leukemia, childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood acute myeloid leukemia", "shortest_name_length": 13}
{"curie": "MONDO:0011364", "names": ["DFNB16", "autosomal recessive deafness 16", "Deafness, Autosomal Recessive 16", "DEAFNESS, AUTOSOMAL RECESSIVE 16", "deafness, autosomal recessive 16", "deafness, autosomal recessive type 16", "autosomal recessive nonsyndromic deafness 16", "STRC autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 16", "autosomal recessive nonsyndromic deafness type 16", "autosomal recessive nonsyndromic deafness caused by mutation in STRC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 16", "shortest_name_length": 6}
{"curie": "UMLS:C5418813", "names": ["Advanced Malignant Skin Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Malignant Skin Neoplasm", "shortest_name_length": 32}
{"curie": "MONDO:0019414", "names": ["BRESEK syndrome", "Bresek Syndrome", "BRESHECK syndrome", "Bresheck Syndrome", "X-linked mental retardation Reish type", "Brain anomaly, severe mental retardation, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia syndrome", "brain anomaly, severe intellectual disability, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia syndrome", "Brain anomaly, severe intellectual disability, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia syndrome", "BRESEK (brain anomaly, severe mental retardation, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia) syndrome", "Brain anomaly, severe intellectual disability, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia syndrome (disorder)", "brain anomaly, severe intellectual disability, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia syndrome (diagnosis)", "Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear-Eye Anomalies, Cleft Palate-Cryptorchidism, And Kidney Dysplasia-Hypoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "BRESEK syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0010360", "names": ["PARK12", "PARKINSON DISEASE 12", "parkinson disease 12", "Parkinson disease 12", "Parkinson Disease 12", "Parkinson disease, X-linked", "PARKINSON DISEASE, X-LINKED", "Parkinson Disease, X-Linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parkinson disease 12", "shortest_name_length": 6}
{"curie": "MONDO:0043114", "names": ["Landy Donnai syndrome", "Landy-Donnai syndrome", "Hydrops, ectrodactyly, syndactyly, duplication of the great toes", "hydrops, ectrodactyly, syndactyly, duplication of the great toes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Landy-Donnai syndrome", "shortest_name_length": 21}
{"curie": "MONDO:0009083", "names": ["Mengel-Konigsmark syndrome", "Ear deformity and conductive hearing loss", "conductive deafness - malformed external ear", "conductive deafness with malformed external ear", "familial congenital moderate neural hearing loss", "Deafness, Conductive, with Malformed External Ear", "DEAFNESS, CONDUCTIVE, WITH MALFORMED EXTERNAL EAR", "deafness, conductive, with malformed external EAR", "conductive hearing loss and malformed low-set ears", "conductive deafness-malformed external ear syndrome", "conductive hearing loss-malformed external ear syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "conductive deafness-malformed external ear syndrome", "shortest_name_length": 26}
{"curie": "MONDO:0023865", "names": ["cornea infection", "infection cornea", "Corneal infection", "corneal infection", "Corneal Infection", "corneal infections", "Infection of cornea", "infection of cornea", "infective keratitis", "Corneal infection NOS", "Corneal infection (disorder)", "corneal infection (diagnosis)", "keratitis caused by infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal infection", "shortest_name_length": 16}
{"curie": "UMLS:C0153790", "names": ["Stage I Subdiaphragmatic Hodgkin Lymphoma", "Hodgkin disease of intrapelvic lymph nodes", "Stage I Subdiaphragmatic Hodgkin's Disease", "Hodgkin lymphoma of intrapelvic lymph nodes", "Stage I Subdiaphragmatic Hodgkin's Lymphoma", "Hodgkin's disease of intrapelvic lymph nodes", "Stage I Hodgkin's Disease below the Diaphragm", "Stage I Hodgkin's Lymphoma below the Diaphragm", "Hodgkin's disease, NOS of intrapelvic lymph nodes", "Ann Arbor Stage I Subdiaphragmatic Hodgkin Lymphoma", "Hodgkin lymphoma of intrapelvic lymph nodes (diagnosis)", "Hodgkin's disease of intrapelvic lymph nodes (disorder)", "Hodgkin's disease, unspecified type, intrapelvic lymph nodes", "Hodgkin's disease, unspecified type, involving intrapelvic lymph nodes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's disease of intrapelvic lymph nodes", "shortest_name_length": 41}
{"curie": "MONDO:0030818", "names": ["SPGF73", "spermatogenic failure 73", "SPERMATOGENIC FAILURE 73"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 73", "shortest_name_length": 6}
{"curie": "UMLS:C1511270", "names": ["Borderline Ovarian Serous Tumor with Microinvasion", "Borderline Ovarian Serous Neoplasm with Microinvasion", "Borderline Ovarian Serous Tumor/Atypical Proliferative Ovarian Serous Tumor with Microinvasion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Ovarian Serous Tumor/Atypical Proliferative Ovarian Serous Tumor with Microinvasion", "shortest_name_length": 50}
{"curie": "MONDO:0021283", "names": ["Mediastinal Immature Teratoma", "Immature Mediastinal Teratoma", "malignant mediastinal teratoma", "mediastinum malignant teratoma", "Immature Teratoma of Mediastinum", "Malignant teratoma of mediastinum", "malignant teratoma of mediastinum", "Immature Teratoma of the Mediastinum", "malignant teratoma of the mediastinum", "mediastinal immature malignant teratoma", "immature malignant teratoma of mediastinum", "Malignant teratoma of mediastinum (disorder)", "malignant teratoma of mediastinum (diagnosis)", "immature malignant teratoma of the mediastinum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant teratoma of mediastinum", "shortest_name_length": 29}
{"curie": "UMLS:C0333374", "names": ["Crypt abscess", "Crypt Abscess", "Crypt abscesses", "Crypt abscess (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Crypt abscess (morphologic abnormality)", "shortest_name_length": 13}
{"curie": "UMLS:C0406526", "names": ["neuropathic diabetic foot ulcer", "Neuropathic diabetic ulcer - foot", "neuropathic diabetic foot ulcer (diagnosis)", "Neuropathic ulcer of foot due to diabetes mellitus", "Neuropathic ulcer of foot due to diabetes mellitus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neuropathic ulcer of foot due to diabetes mellitus", "shortest_name_length": 31}
{"curie": "UMLS:C4053857", "names": ["Voiding Disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Voiding Disorders", "shortest_name_length": 17}
{"curie": "MONDO:0009040", "names": ["Lin-Gettig syndrome", "Craniosynostosis-Mental Retardation Syndrome of Lin and Gettig", "craniosynostosis-mental retardation syndrome of Lin and Gettig", "CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG", "craniosynostosis-intellectual disability syndrome of Lin and Gettig", "craniosynostosis-intellectual disability syndrome of 51N and Gettig"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniosynostosis-intellectual disability syndrome of 51N and Gettig", "shortest_name_length": 19}
{"curie": "UMLS:C5446481", "names": ["Metastatic Anal Canal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Anal Canal Squamous Cell Carcinoma", "shortest_name_length": 45}
{"curie": "UMLS:C1518186", "names": ["Malignant Lymphoma, Convoluted"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Lymphoma, Convoluted", "shortest_name_length": 30}
{"curie": "MONDO:0100475", "names": ["severe ichthyosis vulgaris"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe ichthyosis vulgaris", "shortest_name_length": 26}
{"curie": "UMLS:C4725801", "names": ["Recurrent Malignant Bone Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Malignant Bone Neoplasm", "shortest_name_length": 33}
{"curie": "MONDO:0003813", "names": ["Ovarian Papillary Tumor", "ovarian papillary tumor", "Ovarian papillary tumor", "Papillary tumor of Ovary", "Ovarian papillary tumour", "Papillary Tumor of Ovary", "ovarian papillary tumour", "papillary tumor of ovary", "ovarian papillary neoplasm", "Ovarian Papillary Neoplasm", "papillary neoplasm of ovary", "Papillary Neoplasm of Ovary", "Papillary Tumor of the Ovary", "papillary tumor of the ovary", "Papillary Neoplasm of the Ovary", "papillary neoplasm of the ovary", "ovarian papillary tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian papillary tumor", "shortest_name_length": 23}
{"curie": "UMLS:C0855141", "names": ["Refractory Nodal Marginal Zone Lymphoma", "Nodal Marginal Zone B-Cell Lymphoma Refractory", "Refractory Nodal Marginal Zone B-Cell Lymphoma", "Nodal marginal zone B-cell lymphoma refractory"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nodal marginal zone B-cell lymphoma refractory", "shortest_name_length": 39}
{"curie": "MONDO:0044926", "names": ["Cancer of Oropharynx", "oropharynx carcinoma", "cancer of oropharynx", "Oropharyngeal Cancer", "oropharyngeal cancer", "Oropharynx Carcinoma", "Carcinoma of Oropharynx", "Oropharyngeal Carcinoma", "carcinoma of oropharynx", "oropharyngeal carcinoma", "cancer of the oropharynx", "Cancer of the Oropharynx", "carcinoma of the oropharynx", "oropharyngeal throat cancer", "Carcinoma of the Oropharynx", "Oropharyngeal Throat Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oropharyngeal carcinoma", "shortest_name_length": 20}
{"curie": "MONDO:0006739", "names": ["ascites tumor", "Ascites tumors", "Ehrlich's tumor", "Ehrlich's tumour", "Ehrlich Ascites Tumor", "Ascites Tumor, Ehrlich", "Tumor, Ehrlich Ascites", "ehrlich tumor carcinoma", "Ehrlich tumor carcinoma", "Ehrlich Tumor Carcinoma", "Carcinoma, Ehrlich Tumor", "Ehrlich tumour carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ehrlich tumor carcinoma", "shortest_name_length": 13}
{"curie": "MONDO:0017851", "names": ["EKV", "PSEK", "EKVP", "Greither Disease", "Greither's disease", "Darier-Gottron disease", "Congenital poikiloderma", "Mendes De Costa Syndrome", "Mendes da Costa syndrome", "Erythrokeratoderma variabilis", "Erythrokeratodermia variabilis", "erythrokeratodermia variabilis", "Erythrokeratodermia Variabilis", "ERYTHROKERATODERMIA VARIABILIS", "Erythro et Keratodermia Variabilis", "Erythrokeratodermia Figurata Variabilis", "erythrokeratodermia Figurata variabilis", "keratoderma palmoplantaris transgrediens", "Keratoderma palmoplantaris transgrediens", "Erythrokeratodermia variabilis (disorder)", "progressive symmetric erythrokeratodermia", "Progressive symmetric erythrokeratodermia", "Progressive Symmetric Erythrokeratodermia", "Erythrokeratodermia, Progressive Symmetric", "erythrokeratodermia progressiva symmetrica", "erythrokeratodermia, progressive symmetric", "Erythrokeratodermia progressiva symmetrica", "ERYTHROKERATODERMIA, PROGRESSIVE SYMMETRIC", "ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA", "erythrokeratodermia variabilis ET progressiva", "keratosis extremitatum hereditaria progrediens", "erythrokeratodermia variabilis, Mendes da Costa type", "Erythrokeratodermia variabilis, Mendes da Costa type", "keratosis palmoplantaris transgrediens et progrediens", "KERATOSIS PALMOPLANTARIS TRANSGREDIENS ET PROGREDIENS", "Keratosis palmoplantaris transgrediens et progrediens", "keratosis palmoplantaris transgrediens Et progrediens", "progressive symmetric erythrokeratodermia, Gottron type", "Progressive symmetric erythrokeratodermia, Gottron type", "ERYTHROKERATODERMIA VARIABILIS WITH ERYTHEMA GYRATUM REPENS", "erythrokeratodermia variabilis with erythema Gyratum Repens", "erythrokeratodermia variabilis with erythema gyratum repens", "Erythrokeratodermia Variabilis with Erythema Gyratum Repens", "erythrokeratodermia Figurata, congenital familial, in plaques", "erythrokeratodermia figurata, congenital familial, in plaques", "ERYTHROKERATODERMIA FIGURATA, CONGENITAL FAMILIAL, IN PLAQUES", "Erythrokeratodermia Figurata, Congenital Familial, in Plaques"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythrokeratodermia variabilis", "shortest_name_length": 3}
{"curie": "MONDO:0002635", "names": ["gum disease", "Parodontosis", "Parodontoses", "parodontosis", "PERIODONTAL DISEASE", "periodontal disease", "Periodontal disease", "Periodontal Disease", "Periodontal Diseases", "Disease, Periodontal", "Periodontal Disorder", "periodontium disease", "periodontal disorder", "periodontal diseases", "Diseases, Periodontal", "periodontium disorder", "disease of periodontium", "disorder of periodontium", "Periodontal disease, NOS", "Periodontal disorder NOS", "Periodontal disease (disorder)", "periodontal disease (diagnosis)", "Periodontal disease, unspecified", "periodontium disease or disorder", "disease (or disorder); parodontal", "disease (or disorder); periodontal", "disease or disorder of periodontium", "Disease of supporting structures of teeth", "disease of supporting structures of teeth", "Disease of supporting structures of teeth, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "periodontal disorder", "shortest_name_length": 11}
{"curie": "UMLS:C5447975", "names": ["Recurrent Malignant Genitourinary System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Malignant Genitourinary System Neoplasm", "shortest_name_length": 49}
{"curie": "MONDO:0001939", "names": ["Pseudopyogenic granuloma", "Pseudopyogenic Granuloma", "Angiolymphoid hyperplasia", "Pseudopyogenic Granulomas", "GRANULOMA, PSEUDOPYOGENIC", "angiolymphoid hyperplasia", "Granuloma, Pseudopyogenic", "Granulomas, Pseudopyogenic", "Skin Epithelioid Hemangioma", "skin epithelioid hemangioma", "GRANULOMA, PYOGENIC ATYPICAL", "epithelioid hemangioma of skin", "Epithelioid hemangioma of skin", "Epithelioid Hemangioma of Skin", "Histiocytoid hemangioma of skin", "Histiocytoid Hemangioma of Skin", "histiocytoid hemangioma of skin", "Epithelioid haemangioma of skin", "LYMPHOFOLLICULOSIS, EOSINOPHLIC", "Histiocytoid haemangioma of skin", "Pseudopyogenic granuloma of skin", "Angiolymphoid Hyperplasia of Skin", "angiolymphoid hyperplasia of skin", "Epithelioid Hemangioma of the Skin", "epithelioid hemangioma of the skin", "Histiocytoid Hemangioma of the Skin", "Angiolymphoid Cutaneous Hyperplasia", "angiolymphoid cutaneous hyperplasia", "histiocytoid hemangioma of the skin", "Angiolymphoid Cutaneous hyperplasia", "zone of skin histiocytoid hemangioma", "Angiolymphoid Hyperplasia of the Skin", "angiolymphoid hyperplasia of the skin", "histiocytoid hemangioma of zone of skin", "HYPERPLASIA, ANGIOLYMPHOID SUBCUTANEOUS", "Epithelioid hemangioma of skin (disorder)", "angiolymphoid hyperplasia with eosinophilia", "Angiolymphoid Hyperplasia with Eosinophilia", "Angiolymphoid hyperplasia with eosinophilia of skin", "angiolymphoid hyperplasia with eosinophilia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin epithelioid hemangioma", "shortest_name_length": 24}
{"curie": "MONDO:0810000", "names": ["Choroid Neovascularization", "Neovascularization, Choroid", "Choroid Neovascularizations", "choroidal neovascularization", "Choroidal neovascularisation", "Choroidal Neovascularization", "Choroidal neovascularization", "Neovascularization, Choroidal", "Neovascularization, choroidal", "Choroidal Neovascularizations", "Choroidal neovascular membrane", "choroidal neovascular membrane", "choroidal membranes neovascular", "Choroidal neovascular membrane (diagnosis)", "retinal neovascularization choroidal neovascular membrane"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choroidal neovascularization", "shortest_name_length": 26}
{"curie": "MONDO:0014083", "names": ["AGM7", "agammaglobulinemia 7", "PIK3R1 autosomal agammaglobulinemia", "AGAMMAGLOBULINEMIA 7, AUTOSOMAL RECESSIVE", "agammaglobulinemia 7, autosomal recessive", "autosomal agammaglobulinemia caused by mutation in PIK3R1", "agammaglobulinemia, autosomal recessive, due to PIK3R1 defect", "AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO PIK3R1 DEFECT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "agammaglobulinemia 7, autosomal recessive", "shortest_name_length": 4}
{"curie": "EFO:0009658", "names": ["adverse effect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adverse effect", "shortest_name_length": 14}
{"curie": "UMLS:C5420309", "names": ["Unresectable Pleural Biphasic Mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Pleural Biphasic Mesothelioma", "shortest_name_length": 42}
{"curie": "MONDO:0004269", "names": ["breast cystic hypersecretory carcinoma", "cystic hypersecretory carcinoma of the breast", "cystic hypersecretory duct carcinoma of the breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast cystic hypersecretory carcinoma", "shortest_name_length": 38}
{"curie": "MONDO:0006003", "names": ["Body of uterus Ca", "endometrial cancer", "Corpus Uteri Cancer", "corpus uteri cancer", "Uterine cancer, body", "Uterine Corpus Cancer", "uterine corpus cancer", "body of uterus cancer", "Cancer of uterine body", "cancer of body of uterus", "Cancer of body of uterus", "cancer of the corpus uteri", "Cancer of the Corpus Uteri", "Malignant Uterine Body Tumor", "Malignant Corpus Uteri Tumor", "Malignant Uterine Corpus Tumor", "Malignant Corpus Uteri Neoplasm", "Malignant Uterine Body Neoplasm", "malignant tumor of corpus uteri", "Malignant Tumor of Uterine Body", "Malignant Uterine Corpus Neoplasm", "Malignant tumor of body of uterus", "malignant body of uterus neoplasm", "malignant neoplasm of corpus uteri", "Malignant tumour of body of uterus", "Malignant Neoplasm of Uterine Body", "Malignant neoplasm of corpus uteri", "Malignant Tumor of the Uterine Body", "Malignant neoplasm of body of uterus", "malignant neoplasm of body of uterus", "Malignant Neoplasm of the Uterine Body", "uterine (including endometrial) cancer", "Uterine (Including Endometrial) Cancer", "malignant neoplasm of corpus uteri (diagnosis)", "Malignant neoplasm of corpus uteri, unspecified", "Malignant neoplasm of body of uterus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine corpus cancer", "shortest_name_length": 17}
{"curie": "MONDO:0005391", "names": ["WED", "RLS", "Ekbom", "restless leg", "LEGS RESTLESS", "RESTLESS LEGS", "Legs restless", "restless legs", "Restless legs", "Restless Legs", "Ekbom syndrome", "ekbom syndrome", "ekbom's syndrome", "Willis-Ekbom Disease", "Willis Ekbom Disease", "Willis-Ekbom disease", "Willis-Ekbom Syndrome", "Disease, Willis-Ekbom", "restless leg syndrome", "RESTLESS LEG SYNDROME", "restless leg disorder", "Restless leg syndrome", "Restless Leg Syndrome", "Disease, Willis Ekbom", "Willis Ekbom Syndrome", "Syndrome, Restless Leg", "Restless legs syndrome", "restless legs syndrome", "Restless Legs Syndrome", "Syndrome, Willis Ekbom", "Syndrome, Willis-Ekbom", "Syndrome restless legs", "SYNDROME RESTLESS LEGS", "restless legs; syndrome", "syndrome; restless legs", "Wittmaack Ekbom Syndrome", "Restless legs (disorder)", "Wittmaack-Ekbom Syndrome", "Wittmaack-Ekbom syndrome", "Syndrome, Wittmaack-Ekbom", "Syndrome, Wittmaack Ekbom", "restless leg syndrome (RLS)", "Restless legs syndrome (RLS)", "restless leg syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "restless legs syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C4525134", "names": ["Stage II Rectal Cancer", "Stage II Rectal Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Rectal Cancer AJCC v8", "shortest_name_length": 22}
{"curie": "UMLS:C0272247", "names": ["Biclonal gammopathy", "Biclonal Gammopathy", "biclonal gammopathy", "Double M peak gammopathy", "Biclonal gammopathy, NOS", "Biclonal gammopathy (disorder)", "biclonal gammopathy (diagnosis)", "Monoclonal gammopathy with two clones", "Monoclonal (M) protein disease, multiple 'M' protein"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Biclonal gammopathy", "shortest_name_length": 19}
{"curie": "MONDO:0002323", "names": ["Morgan, de", "cherry angioma", "Cherry Angioma", "Senile angioma", "angioma cherry", "Senile ectasia", "Cherry angioma", "Senile Angioma", "angioma senile", "senile angioma", "angioma; senile", "senile; angioma", "Cherry angiomas", "blood skin spot", "de Morgan; spot", "spot; de Morgan", "cherry angiomas", "blood skin spots", "Senile Hemangioma", "de Morgan's spots", "Cherry Hemangioma", "Senile hemangioma", "De Morgan's spots", "hemangioma senile", "senile hemangioma", "Cherry hemangioma", "Hemangioma senile", "cherry hemangioma", "Cherry haemangioma", "cherry hemangiomas", "Haemangioma senile", "blood spots on skin", "Blood spots on skin", "Senile nevus of skin", "Senile naevus of skin", "Campbell de Morgan Spot", "campbell de morgan spot", "Campbell de Morgan spot", "campbell de morgan spots", "Campbell de Morgan spots", "Senile angioma (disorder)", "campbell de morgan angioma", "Campbell de Morgan angioma", "senile hemangioma (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cherry hemangioma", "shortest_name_length": 10}
{"curie": "UMLS:C0743072", "names": ["DEPRESSED PSYCHOSIS", "PSYCHOSIS DEPRESSIVE", "DEPRESSION PSYCHOTIC", "Depression psychotic", "Psychotic depression", "psychotic depression", "DEPRESSIVE PSYCHOSIS", "PSYCHOTIC DEPRESSION", "Depression;psychotic", "depression psychotic", "Psychosis;depressive", "depressive psychosis", "Psychosis depressive", "depressive; psychosis", "psychosis; depressive", "depression; psychotic", "Depression, psychotic", "psychotic; depression"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Depression, psychotic", "shortest_name_length": 19}
{"curie": "MONDO:0008436", "names": ["SNDNS", "sneddon syndrome", "SNEDDON SYNDROME", "Sneddon syndrome", "Sneddon Syndrome", "Syndrome, Sneddon", "sneddons syndrome", "Sneddon's syndrome", "sneddon's syndrome", "Ehrmann-Sneddon syndrome", "Ehrmann Sneddon syndrome", "Sneddon-Champion Syndrome", "Sneddon Champion Syndrome", "Syndrome, Sneddon-Champion", "Livedo Reticularis, Systemic Involvement", "Livedo racemosa and cerebrovascular accident", "livedo racemosa and cerebrovascular accidents", "cerebro-vascular lesions and livedo reticularis", "livedo reticularis and cerebrovascular accidents", "Livedo Reticularis And Cerebrovascular Accidents", "LIVEDO RETICULARIS AND CEREBROVASCULAR ACCIDENTS", "livedo racemosa-cerebrovascular accident syndrome", "Livedo racemosa-cerebrovascular accident syndrome", "Livedo reticularis-cerebrovascular accident syndrome", "livedo reticularis-cerebrovascular accident syndrome", "Idiopathic livedo reticularis with systemic involvement", "idiopathic livedo reticularis with systemic involvement", "Livedo reticularis and cerebrovascular accident syndrome", "Idiopathic livedo reticularis with systemic involvement (disorder)", "Livedo reticularis and cerebrovascular accident syndrome (disorder)", "Livedo reticularis and cerebrovascular accident syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sneddon syndrome", "shortest_name_length": 5}
{"curie": "EFO:0010725", "names": ["aseptic loosening"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aseptic loosening", "shortest_name_length": 17}
{"curie": "MONDO:0011083", "names": ["kersey syndrome", "Kersey syndrome", "trichodental syndrome", "Trichodental syndrome", "TRICHODENTAL DYSPLASIA", "TRICHODENTAL dysplasia", "Tricho-dental syndrome", "Trichodental dysplasia", "Tricho-dental dysplasia", "Trichodental syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichodental syndrome", "shortest_name_length": 15}
{"curie": "UMLS:C1708656", "names": ["Laryngeal Carcinosarcoma", "Laryngeal Sarcomatoid Carcinoma", "Laryngeal Squamous Cell Carcinoma, Spindle Cell Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laryngeal Squamous Cell Carcinoma, Spindle Cell Variant", "shortest_name_length": 24}
{"curie": "MONDO:0005247", "names": ["UTI", "uti", "utis", "urine; infected", "urinary infection", "Urinary infection", "infected; urinary", "urinary; infection", "Urinary tract infection", "Infection urinary tract", "URINARY TRACT INFECTION", "Urinary Tract Infection", "INFECTION URINARY TRACT", "urinary tract infection", "Urinary tract infections", "infection, urinary tract", "Infection, Urinary Tract", "Tract Infection, Urinary", "Urinary Tract Infections", "infection; urinary tract", "urinary tract infections", "Infections, Urinary Tract", "Tract Infections, Urinary", "Infection of urinary tract", "Urinary tract infection NOS", "tract, infection of urinary", "Urinary tract infection, NOS", "urinary tract infection (UTI)", "UTI - Urinary tract infection", "Urinary Tract Infectious Disease", "Urinary tract infectious disease", "urinary tract infectious disease", "bacterial urinary tract infection", "urinary tract infection (disease)", "urinary tract infection (diagnosis)", "Urinary tract infectious disease, NOS", "Urinary tract infection; site not specified", "Urinary tract infection, site not specified", "bacterial urinary tract infection (disease)", "Urinary tract infectious disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bacterial urinary tract infection", "shortest_name_length": 3}
{"curie": "UMLS:C4521878", "names": ["Stage III", "Stage III Pancreatic Cancer", "Stage III Pancreatic Cancer AJCC v8", "Stage III Exocrine Pancreatic Cancer AJCC v8", "Stage III Exocrine Pancreatic Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Pancreatic Cancer AJCC v8", "shortest_name_length": 9}
{"curie": "MONDO:0013604", "names": ["MYP21", "ZNF644 myopia (disease)", "MYOPIA 21, AUTOSOMAL DOMINANT", "myopia 21, autosomal dominant", "myopia (disease) caused by mutation in ZNF644"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopia 21, autosomal dominant", "shortest_name_length": 5}
{"curie": "UMLS:C2986699", "names": ["Stage I Ovarian Low Malignant Potential Tumor", "stage I ovarian low malignant potential tumor", "stage I ovarian tumors of low malignant potential", "ovarian tumors of low malignant potential, stage I", "Stage I Borderline Ovarian Surface Epithelial-Stromal Tumor", "stage I borderline ovarian surface epithelial-stromal tumor", "borderline ovarian surface epithelial-stromal tumor, stage I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Borderline Ovarian Surface Epithelial-Stromal Tumor", "shortest_name_length": 45}
{"curie": "MONDO:0014473", "names": ["MCPH13", "primary autosomal recessive microcephaly 13", "MICROCEPHALY 13, PRIMARY, AUTOSOMAL RECESSIVE", "microcephaly 13, primary, autosomal recessive", "CENPE autosomal recessive primary microcephaly", "autosomal recessive primary microcephaly caused by mutation in CENPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly 13, primary, autosomal recessive", "shortest_name_length": 6}
{"curie": "MONDO:0008888", "names": ["bronchomalacia", "Bronchomalacia", "BRONCHOMALACIA", "Bronchomalacias", "Bronchomalacia NOS", "tracheobronchomalacia", "Bronchi Chondromalacia", "Bronchi Chondromalacias", "Chondromalacia of Bronchi", "Bronchomalacia (disorder)", "bronchomalacia (diagnosis)", "Williams-Campbell syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Williams-Campbell syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0015222", "names": ["syndromic respiratory or mediastinal malformation", "syndrome associated with respiratory or mediastinal malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic respiratory or mediastinal malformation", "shortest_name_length": 49}
{"curie": "MONDO:0019867", "names": ["Trisomy 8 mosaic", "Mosaic trisomy 8", "mosaic trisomy 8", "Warkany syndrome", "trisomy 8 mosaic", "Trisomy 8 Mosaicism", "Trisomy 8 mosaicism", "trisomy 8 mosaicism", "Mosaic trisomy type 8", "Mosaic trisomy 8 syndrome", "Mosaic trisomy chromosome 8", "Chromosome 8, mosaic trisomy", "trisomy 8 mosaicism (diagnosis)", "Mosaic trisomy 8 syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mosaic trisomy 8", "shortest_name_length": 16}
{"curie": "MONDO:0014613", "names": ["PFBMFT3", "PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 3", "pulmonary fibrosis and/or bone marrow failure, TELOMERE-RELATED, 3", "pulmonary fibrosis and/or bone marrow failure, Telomere-related, 3", "RTEL1 pulmonary fibrosis and/or bone marrow failure, Telomere-related", "pulmonary fibrosis and/or bone marrow failure, Telomere-related, type 3", "pulmonary fibrosis and/or bone marrow failure, Telomere-related caused by mutation in RTEL1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary fibrosis and/or bone marrow failure, Telomere-related, 3", "shortest_name_length": 7}
{"curie": "MONDO:0013082", "names": ["NEUROBLASTOMA WITH HIRSCHSPRUNG DISEASE", "neuroblastoma with Hirschsprung disease", "Neuroblastoma with Hirschsprung disease", "Hirschsprung disease ganglioneuroblastoma", "Hirschsprung disease-ganglioneuroblastoma syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hirschsprung disease-ganglioneuroblastoma syndrome", "shortest_name_length": 39}
{"curie": "MONDO:0014288", "names": ["JBTS21", "JOUBERT SYNDROME 21", "Joubert syndrome 21", "CSPP1 Joubert syndrome", "Joubert syndrome type 21", "Joubert syndrome caused by mutation in CSPP1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome 21", "shortest_name_length": 6}
{"curie": "UMLS:C1336712", "names": ["testicular choriocarcinoma and embryonal carcinoma", "embryonal carcinoma and choriocarcinoma, testicular", "choriocarcinoma and embryonal carcinoma of the testis", "testis cancer, embryonal carcinoma and choriocarcinoma", "testis cancer, choriocarcinoma and embryonal carcinoma", "Mixed Choriocarcinoma and Embryonal Carcinoma of Testis", "testicle cancer, choriocarcinoma and embryonal carcinoma", "Testicular Mixed Choriocarcinoma and Embryonal Carcinoma", "testicular cancer, embryonal carcinoma and choriocarcinoma", "testicular cancer, choriocarcinoma and embryonal carcinoma", "Mixed Choriocarcinoma and Embryonal Carcinoma of the Testis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular Mixed Choriocarcinoma and Embryonal Carcinoma", "shortest_name_length": 50}
{"curie": "MONDO:0006547", "names": ["RASH", "Rash", "rash", "spots", "rashes", "Rashes", "exanthem", "rash NOS", "Eruption", "Exanthem", "Rash NOS", "EXANTHEM", "ERUPTION", "skin rash", "EXANTHEMA", "Rash, NOS", "Skin Rash", "exanthema", "exanthems", "Exanthema", "skin Rash", "Skin rash", "Rash, Skin", "exanthemas", "Skin rashes", "Exanthemata", "exanthemata", "efflorescence", "skin eruption", "Efflorescence", "Skin Eruption", "Skin eruption", "SKIN ERUPTION", "eruption; skin", "skin; eruption", "rash (symptom)", "Eruption of skin", "Cutaneous eruption", "cutaneous eruption", "Rash (nonspecific)", "Cutaneous Eruption", "exanthem (disease)", "cutaneous eruptions", "exanthem (diagnosis)", "Breaking out - eruption", "Cutaneous eruption, NOS", "skin eruption (diagnosis)", "cutaneous eruption on skin", "Eruption of skin (disorder)", "Rash and other nonspecific skin eruption"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exanthem", "shortest_name_length": 4}
{"curie": "MONDO:0700195", "names": ["Rous Sarcoma", "rous sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rous sarcoma", "shortest_name_length": 12}
{"curie": "UMLS:C0948065", "names": ["Periorbital Infection", "Periorbital infection", "periorbital infection", "periorbital; infection", "infection; periorbital", "periorbital infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Periorbital Infection", "shortest_name_length": 21}
{"curie": "MONDO:0014231", "names": ["PARK19", "PARK19B", "PARK19A", "PARK19, FORMERLY", "Park19, formerly", "Parkinson's disease 19A", "DNAJC6 Parkinson disease", "PARKINSON DISEASE 19B, EARLY-ONSET", "Parkinson disease 19B, early-onset", "juvenile onset Parkinson disease 19A", "Parkinson disease 19, juvenile-onset", "Parkinson disease 19A, juvenile-onset", "PARKINSON DISEASE 19A, JUVENILE-ONSET", "juvenile onset Parkinson's disease 19A", "juvenile onset Parkinson disease type 19A", "Parkinson disease caused by mutation in DNAJC6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile onset Parkinson disease 19A", "shortest_name_length": 6}
{"curie": "MONDO:0000928", "names": ["Eyelid Melanoma", "eyelid melanoma", "eyelid; melanoma", "melanoma; eyelid", "palpebra; melanoma", "melanoma of eyelid", "melanoma; palpebra", "Melanoma of Eyelid", "Melanoma of the Eyelid", "melanoma of the eyelid", "malignant eyelid melanoma", "eyelid melanoma (disease)", "Malignant Eyelid Melanoma", "melanoma (disease) of eyelid", "Malignant Melanoma of Eyelid", "Malignant melanoma of eyelid", "malignant melanoma of eyelid", "Malignant Melanoma of the Eyelid", "malignant melanoma of the eyelid", "melanoma of eyelid (physical finding)", "Malignant melanoma of eyelid (disorder)", "malignant melanoma of the eyelid (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eyelid melanoma", "shortest_name_length": 15}
{"curie": "UMLS:C3272659", "names": ["Cystitis Cystica and Glandularis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cystitis Cystica and Glandularis", "shortest_name_length": 32}
{"curie": "UMLS:C1720816", "names": ["Endometrial Disease", "Disease, Endometrial", "Endometrial Diseases", "Diseases, Endometrial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endometrial Diseases", "shortest_name_length": 19}
{"curie": "UMLS:C1336111", "names": ["Stage IA Adenosquamous Lung Cancer", "Stage IA Adenosquamous Lung Carcinoma", "Stage IA Adenosquamous Cell Lung Carcinoma", "Stage IA Adenosquamous Cell Carcinoma of Lung", "Stage IA Lung Adenosquamous Carcinoma AJCC v7", "Stage IA Adenosquamous Cell Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Lung Adenosquamous Carcinoma AJCC v7", "shortest_name_length": 34}
{"curie": "UMLS:C5206465", "names": ["Hypermutated Colorectal Cancer", "Hypermutated Colorectal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypermutated Colorectal Carcinoma", "shortest_name_length": 30}
{"curie": "UMLS:C0280185", "names": ["Recurrent Grade 3 Follicular Lymphoma", "recurrent grade 3 follicular lymphoma", "Relapsed Grade III Follicular Lymphoma", "Relapsed Follicular Large Cell Lymphoma", "Recurrent Grade III Follicular Lymphoma", "relapsed follicular large cell lymphoma", "follicular large cell lymphoma, relapsed", "Recurrent Follicular Large Cell Lymphoma", "follicular large cell lymphoma, recurrent", "Relapsed Grade III Follicular Large Cell Lymphoma", "Recurrent Grade III Follicular Large Cell Lymphoma", "recurrent grade III follicular large cell lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Grade 3 Follicular Lymphoma", "shortest_name_length": 37}
{"curie": "UMLS:C0264515", "names": ["Necrotic pneumonia", "pneumonia; necrotic", "necrotic; pneumonia", "pneumonia gangrenous", "Gangrenous pneumonia", "necrotized pneumonia", "necrotising pneumonia", "Necrotising pneumonia", "Pneumonia necrotizing", "Necrotizing pneumonia", "Pneumonia necrotising", "gangrenous; pneumonia", "Necrotizing Pneumonia", "necrotizing pneumonia", "pneumonia; gangrenous", "pneumonia necrotizing", "Necrotizing Pneumonias", "Pneumonia, Necrotizing", "Pneumonias, Necrotizing", "Gangrenous pneumonia (disorder)", "Gangrenous pneumonia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pneumonia, Necrotizing", "shortest_name_length": 18}
{"curie": "MONDO:0011961", "names": ["HSN1B", "HSAN1B", "hereditary sensory neuropathy type 1B", "hereditary sensory neuropathy type IB", "neuropathy, hereditary sensory, type IB", "NEUROPATHY, HEREDITARY SENSORY, TYPE IB", "neuropathy, hereditary sensory, type 1B", "Neuropathy, Hereditary Sensory, Type IB", "HSAN with cough and gastroesophageal reflux", "hereditary sensory and autonomic neuropathy type 1B", "hereditary sensory and autonomic neuropathy type IB", "Hereditary sensory and autonomic neuropathy type 1B", "Hereditary sensory and autonomic neuropathy type IB", "neuropathy, hereditary sensory and autonomic, type 1B", "Neuropathy, Hereditary Sensory And Autonomic, Type IB", "NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IB", "HSAN1B - hereditary sensory and autonomic neuropathy type 1B", "Hereditary sensory and autonomic neuropathy type 1B (disorder)", "Hereditary sensory and autonomic neuropathy type 1 with cough and gastroesophageal reflux", "hereditary sensory and autonomic neuropathy type 1 with cough and gastroesophageal reflux", "Hereditary sensory and autonomic neuropathy type 1 with cough and gastrooesophageal reflux", "Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux", "neuropathy, hereditary sensory and autonomic, type I, with cough and gastroesophageal reflux", "NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, WITH COUGH AND GASTROESOPHAGEAL REFLUX"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary sensory and autonomic neuropathy type 1B", "shortest_name_length": 5}
{"curie": "MONDO:0014423", "names": ["IMD26", "DNA PKcs deficiency", "DNA-PKcs Deficiency", "immunodeficiency 26", "SCID due to DNA-PKcs deficiency", "Severe combined immunodeficiency due to DNA-PKcs deficiency", "severe combined immunodeficiency due to DNA-PKcs deficiency", "Immunodeficiency 26 with or without Neurologic Abnormalities", "IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES", "immunodeficiency 26 with or without neurologic abnormalities", "immunodeficiency 26, with or without neurologic abnormalities", "severe combined immunodeficiency disease due to DNA-PKCS deficiency", "severe combined immunodeficiency due to DNA dependent protein kinase catalytic subunit deficiency", "severe combined immunodeficiency due to DNA dependent protein kinase catalytic subunit deficiency (diagnosis)", "Severe combined immunodeficiency due to deoxyribonucleic acid dependent protein kinase catalytic subunit deficiency", "Severe combined immunodeficiency due to deoxyribonucleic acid dependent protein kinase catalytic subunit deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe combined immunodeficiency due to DNA-PKcs deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0020816", "names": ["Miliaria papulosa", "miliaria papulosa", "Miliaria papulosa (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "miliaria papulosa", "shortest_name_length": 17}
{"curie": "UMLS:C0858833", "names": ["endometrial hypertrophy", "Endometrial hypertrophy", "hypertrophy; endometrial", "endometrium; hypertrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endometrial hypertrophy", "shortest_name_length": 23}
{"curie": "MONDO:0016202", "names": ["DRRD", "Autosomal dominant rhegmatogenous retinal detachment", "autosomal dominant rhegmatogenous retinal detachment", "retinal detachment rhegmatogenous autosomal dominant", "rhegmatogenous retinal detachment, autosomal dominant", "RHEGMATOGENOUS RETINAL DETACHMENT, AUTOSOMAL DOMINANT", "Rhegmatogenous Retinal Detachment, Autosomal Dominant", "Autosomal dominant rhegmatogenous retinal detachment (disorder)", "Autosomal dominant rhegmatogenous retinal detachment (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant rhegmatogenous retinal detachment", "shortest_name_length": 4}
{"curie": "MONDO:0011410", "names": ["HIRSCHSPRUNG DISEASE WITH HEART DEFECTS, LARYNGEAL ANOMALIES, AND PREAXIAL POLYDACTYLY", "Hirschsprung disease with heart defects, laryngeal anomalies, and preaxial polydactyly", "Hirschsprung Disease with Heart Defects, Laryngeal Anomalies, and Preaxial Polydactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hirschsprung disease with heart defects, laryngeal anomalies, and preaxial polydactyly", "shortest_name_length": 86}
{"curie": "UMLS:C2981373", "names": ["Stage IIIB Esophageal Adenocarcinoma", "Stage IIIB Esophageal Adenocarcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Esophageal Adenocarcinoma AJCC v7", "shortest_name_length": 36}
{"curie": "UMLS:C0473223", "names": ["aluminum intoxication", "Aluminum intoxication", "aluminium intoxication", "Aluminium intoxication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aluminium intoxication", "shortest_name_length": 21}
{"curie": "MONDO:0018793", "names": ["type 1 condylar hyperplasia", "primary condylar hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary condylar hyperplasia", "shortest_name_length": 27}
{"curie": "UMLS:C4553240", "names": ["Stage II", "Stage II Renal Cell Cancer", "Stage II Renal Cell Cancer AJCC v8", "Stage II Renal Cell Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Renal Cell Cancer AJCC v8", "shortest_name_length": 8}
{"curie": "UMLS:C0855054", "names": ["Metastatic Fibrosarcoma", "Fibrosarcoma metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fibrosarcoma metastatic", "shortest_name_length": 23}
{"curie": "MONDO:0020373", "names": ["CAP", "CTAA1", "Anterior polar cataract", "Cataract anterior polar", "cataract anterior polar", "Cataract, Anterior Polar", "CATARACT, ANTERIOR POLAR", "Polar cataract, anterior", "Cataract, anterior polar", "Anterior polar cataracts 1", "CATARACT, ANTERIOR POLAR, 1", "Cataract, Anterior Polar, 1", "Cataract anterior polar dominant", "Early-onset anterior polar cataract", "early-onset anterior polar cataract", "early-onset anterior subcapsular cataract", "Early-onset anterior subcapsular cataract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early-onset anterior polar cataract", "shortest_name_length": 3}
{"curie": "MONDO:0012331", "names": ["Mgr9", "MGR9", "MIGRAINE WITH AURA, SUSCEPTIBILITY TO, 9", "migraine with aura, susceptibility to, 9", "migraine with aura, susceptibility to, type 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "migraine with aura, susceptibility to, 9", "shortest_name_length": 4}
{"curie": "MONDO:0007965", "names": ["MELANOMA, MALIGNANT FAMILIAL INTRAOCULAR", "Melanoma, Malignant Familial Intraocular", "melanoma, malignant familial intraocular"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melanoma, malignant familial intraocular", "shortest_name_length": 40}
{"curie": "UMLS:C2987507", "names": ["Stage I Gallbladder Cancer", "Stage I Gallbladder Cancer AJCC v7", "Stage I Gallbladder Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Gallbladder Cancer AJCC v7", "shortest_name_length": 26}
{"curie": "MONDO:0022675", "names": ["cataract skeletal anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract skeletal anomalies", "shortest_name_length": 27}
{"curie": "UMLS:C4687638", "names": ["Cardiac Osteosarcoma", "Cardiac Osteogenic Sarcoma", "Heart Extraskeletal Osteosarcoma", "Cardiac Extraskeletal Osteosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiac Extraskeletal Osteosarcoma", "shortest_name_length": 20}
{"curie": "MONDO:0008137", "names": ["OFD10", "OFDS X", "Ofds 10", "OFD syndrome 10", "Figuera syndrome", "orofaciodigital syndrome X", "OROFACIODIGITAL SYNDROME X", "Orofaciodigital Syndrome X", "orofaciodigital syndrome 10", "oral facial digital syndrome 10", "orofaciodigital syndrome type X", "oral-facial-digital syndrome 10", "Orofaciodigital syndrome type 10", "orofaciodigital syndrome type 10", "Oro-facial digital syndrome type 10", "oral-facial-digital syndrome type 10", "Oral-facial-digital syndrome type 10", "oral facial digital syndrome type 10", "ORAL-FACIAL-DIGITAL SYNDROME, TYPE X", "Oral-Facial-Digital Syndrome, Type X", "oral-Facial-digital syndrome, type 10", "orofaciodigital syndrome type Figuera", "OROFACIODIGITAL SYNDROME WITH FIBULAR APLASIA", "Orofaciodigital Syndrome with Fibular Aplasia", "Orofaciodigital syndrome with fibular aplasia", "orofaciodigital syndrome with fibular aplasia", "Oro-facial digital syndrome type 10 (disorder)", "oral-facial-digital syndrome type 10 (diagnosis)", "ORAL-FACIAL-DIGITAL SYNDROME WITH FIBULAR APLASIA", "Oral-Facial-Digital Syndrome with Fibular Aplasia", "oral-Facial-digital syndrome with fibular aplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orofaciodigital syndrome X", "shortest_name_length": 5}
{"curie": "MONDO:0700000", "names": ["ALG9-associated ADPKD", "ALG9 autosomal dominant polycystic kidney disease", "ALG9 related autosomal dominant polycystic kidney disease", "ALG9-associated autosomal dominant polycystic kidney disease", "autosomal dominant polycystic kidney disease caused by mutation in ALG9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ALG9-associated autosomal dominant polycystic kidney disease", "shortest_name_length": 21}
{"curie": "MONDO:0005388", "names": ["pbc", "PBC", "Hanot", "HANOT SYNDROME", "Hanot syndrome", "Hanot; cirrhosis", "bilary cirrhosis", "CIRRHOSIS BILARY", "cirrhosis; Hanot", "Biliary Cirrhosis", "CIRRHOSIS BILIARY", "BILIARY CIRRHOSIS", "Hanot's cirrhosis", "cirrhosis biliary", "Cirrhosis biliary", "biliary cirrhosis", "Biliary cirrhosis", "cirrhosis; biliary", "Cirrhosis, Biliary", "biliary; cirrhosis", "cholangitic cirrhosis", "Cholestatic cirrhosis", "Biliary cirrhosis NOS", "cholestatic cirrhosis", "Cholangitic cirrhosis", "Cirrhosis, cholangitic", "Cirrhosis, cholestatic", "biliary liver cirrhosis", "biliary cirrhosis liver", "Biliary Liver Cirrhosis", "Liver Cirrhoses, Biliary", "Liver Cirrhosis, Biliary", "Biliary cirrhosis primary", "Cirrhosis;biliary;primary", "primary biliary cirrhosis", "PRIMARY BILIARY CIRRHOSIS", "Primary biliary cirrhosis", "Primary Biliary Cirrhosis", "CIRRHOSIS PRIMARY BILIARY", "BILIARY CIRRHOSIS PRIMARY", "biliary cirrhosis primary", "cirrhosis primary biliary", "Biliary Cirrhosis, Primary", "CIRRHOSIS, PRIMARY BILIARY", "Cirrhosis, primary biliary", "biliary cirrhosis, primary", "cirrhosis; biliary, primary", "primary biliary cholangitis", "Primary Biliary Cholangitis", "biliary; cirrhosis, primary", "Primary biliary cholangitis", "Cholangitis, Primary Biliary", "Biliary Cholangitis, Primary", "Biliary cirrhosis (disorder)", "biliary cirrhosis pbc primary", "biliary cirrhosis (diagnosis)", "Primary Biliary Cholangitides", "Biliary cirrhosis, unspecified", "Biliary Cholangitides, Primary", "Cholangitides, Primary Biliary", "PBC- Primary biliary cirrhosis", "primary Bilary cirrhosis (PBC)", "Primary Biliary Cirrhosis (PBC)", "CIRRHOSIS, CHOLANGIOLITIC BILIARY", "familial primary biliary cirrhosis", "primary biliary cirrhosis (diagnosis)", "Primary biliary cholangitis (disorder)", "LIVER, HYPERTROPHIC CIRRHOSIS OF HANOT", "Chronic nonsuppurative destructive cholangitis", "chronic nonsuppurative destructive cholangitis", "chronic non-suppurative destructive cholangitis", "cholangitis; chronic nonsuppurative destructive", "Cholangitis, Chronic Nonsuppurative Destructive", "Chronic Non-Suppurative Destructive Cholangitis", "Chronic non-suppurative destructive cholangitis", "chronic; cholangitis, chronic nonsuppurative destructive, destructive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary biliary cholangitis", "shortest_name_length": 3}
{"curie": "UMLS:C5555706", "names": ["Unresectable Platinum-Resistant Ovarian Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Platinum-Resistant Ovarian Carcinoma", "shortest_name_length": 49}
{"curie": "MONDO:0008180", "names": ["VPI", "Velopharyngeal inadequacy", "velopharyngeal inadequacy", "Velopharyngeal dysfunction", "Velopharyngeal incompetence", "Velopharyngeal Incompetence", "VELOPHARYNGEAL INCOMPETENCE", "velopharyngeal incompetence", "Incompetence, Velopharyngeal", "Velopharyngeal Insufficiency", "Velopharyngeal insufficiency", "velopharyngeal insufficiency", "VELOPHARYNGEAL INSUFFICIENCY", "Insufficiency, Velopharyngeal", "Palatopharyngeal Incompetence", "Palatopharyngeal incompetence", "PALATOPHARYNGEAL INCOMPETENCE", "palatopharyngeal incompetence", "Incompetence, Palatopharyngeal", "Palatopharyngeal insufficiency", "Inadequate Velopharyngeal Closure", "VPI - Velopharyngeal incompetence", "Velopharyngeal Closures, Inadequate", "Velopharyngeal inadequacy (disorder)", "velopharyngeal inadequacy (diagnosis)", "Velopharyngeal incompetence (disorder)", "congenital velopharyngeal incompetence", "Velopharyngeal insufficiency (disorder)", "velopharyngeal insufficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital velopharyngeal incompetence", "shortest_name_length": 3}
{"curie": "UMLS:C3887638", "names": ["Failure to Thrive", "Infant Failure to Thrive", "Failure to thrive (child)", "failure to thrive in infant", "Failure to thrive in infant", "Failure to Thrive in Infant", "Failure to thrive in infant (disorder)", "failure to thrive in infant (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Failure to thrive in infant", "shortest_name_length": 17}
{"curie": "MONDO:0010284", "names": ["MRXSA", "Armfield syndrome", "Mental Retardation, X-Linked, Armfield Type", "ARMFIELD X-LINKED MENTAL RETARDATION SYNDROME", "Armfield X-Linked Mental Retardation Syndrome", "Armfield X-linked mental retardation syndrome", "X-linked intellectual disability Armfield type", "X-linked intellectual disability, Armfield type", "Armfield X-linked intellectual disability syndrome", "syndromic X-linked mental retardation Armfield type", "mental retardation syndrome, X-linked, Armfield type", "mental retardation, X-linked, syndromic, Armfield type", "syndromic X-linked intellectual disability Armfield type", "X-linked intellectual disability Armfield type (disorder)", "intellectual disability syndrome, X-linked, Armfield type", "X-linked intellectual disability Armfield type (diagnosis)", "intellectual disability, X-linked, syndromic, Armfield type", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, ARMFIELD TYPE", "mental retardation syndrome, X-linked, armfield type, X-linked recessive", "intellectual developmental disorder, X-linked, syndromic, Armfield type, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Armfield syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0858552", "names": ["Permanent Spinal Nerve Paralysis", "Spinal nerves paralysis permanent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spinal nerves paralysis permanent", "shortest_name_length": 32}
{"curie": "UMLS:C0948388", "names": ["Dilatation intrahepatic duct acquired"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dilatation intrahepatic duct acquired", "shortest_name_length": 37}
{"curie": "MONDO:0004402", "names": ["glandular-alveolar pattern testicular yolk sac tumor", "Testicular Yolk Sac Tumor, Glandular-Alveolar Pattern", "testicular yolk sac tumor, glandular-alveolar pattern"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular yolk sac tumor, glandular-alveolar pattern", "shortest_name_length": 52}
{"curie": "MONDO:0004917", "names": ["INTERNAL STY", "STY, INTERNAL", "MEIBOMIAN STY", "stye; meibomian", "meibomian; stye", "internal hordeolum", "Meibomian adenitis", "Internal hordeolum", "meibomian adenitis", "infected chalazion", "hordeolum internum", "Hordeolum internum", "Infected chalazion", "HORDEOLUM, INTERNAL", "Stye of inner eyelid", "CHALAZION, SUPPURATING", "tarsal gland hordeolum", "infected meibomian cyst", "Infected meibomian cyst", "Infected Meibomian cyst", "Meibomian cyst infected", "Red bump on inner eyelid", "hordeolum of tarsal gland", "meibomian; cyst, infected", "cyst; meibomian, infected", "infection of meibomian gland", "Infection of meibomian gland", "Internal hordeolum (disorder)", "hordeolum internum (diagnosis)", "Infected cyst of Meibomian gland", "Infected cyst of meibomian gland", "infected cyst of meibomian gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "internal hordeolum", "shortest_name_length": 12}
{"curie": "MONDO:0017932", "names": ["muscular hypertrophy-hepatomegaly-polyhydramnios syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular hypertrophy-hepatomegaly-polyhydramnios syndrome", "shortest_name_length": 57}
{"curie": "MONDO:0011262", "names": ["Rozin hertz Goodman syndrome", "Rozin camptodactyly syndrome", "Rozin Hertz Goodman syndrome", "camptodactyly, joint contractures, facial skeletal defects", "Camptodactyly, joint contractures, facial skeletal defects", "Camptodactyly-joint contractures-facial skeletal defects syndrome", "camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye", "Camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye", "CAMPTODACTYLY, MYOPIA, AND FIBROSIS OF THE MEDIAL RECTUS MUSCLE OF EYE", "Camptodactyly with joint contracture and facial skeletal defect syndrome", "Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye", "shortest_name_length": 28}
{"curie": "UMLS:C0266139", "names": ["H-type congenital tracheoesophageal fistula", "Congenital H-type Tracheoesophageal Fistula", "Congenital H-Type Tracheoesophageal Fistula", "H-type congenital tracheo-oesophageal fistula", "H-type congenital tracheoesophageal fistula (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "H-type congenital tracheoesophageal fistula", "shortest_name_length": 43}
{"curie": "UMLS:C0877237", "names": ["Traumatic fracture", "traumatic fracture", "fractures traumatic", "traumatic fracture (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Traumatic fracture", "shortest_name_length": 18}
{"curie": "OMIM:614036", "names": ["A2MD", "alpha-2-Macroglobulin Deficiency", "ALPHA-2-MACROGLOBULIN DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 4}
{"curie": "UMLS:C5419609", "names": ["Advanced Basal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Basal Cell Carcinoma", "shortest_name_length": 29}
{"curie": "UMLS:C5206558", "names": ["Recurrent Myelofibrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Myelofibrosis", "shortest_name_length": 23}
{"curie": "MONDO:0024271", "names": ["Intestinal helminthiasis", "Helminthiasis;intestinal", "intestinal helminthiasis", "helminthiasis; intestinal", "intestinal; helminthiasis", "Intestinal helminthiasis, NOS", "helminthes; infestation, intestinal", "infestation; helminthes, intestinal", "intestinal helminthiasis (diagnosis)", "Intestinal helminthiasis, unspecified", "intestine parasitic helminthiasis infectious disease", "Intestinal infection due to Class Cestoda and/or Class Trematoda and/or Phylum Nemata", "Intestinal infection caused by Class Cestoda and/or Class Trematoda and/or Phylum Nemata", "Intestinal infection caused by Class Cestoda and/or Class Trematoda and/or Phylum Nemata (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intestinal helminthiasis", "shortest_name_length": 24}
{"curie": "MONDO:0009430", "names": ["ARHP", "Arhr", "ARHR", "ARHR1", "hypophosphatemic rickets, AR", "HYPOPHOSPHATEMIA, AUTOSOMAL RECESSIVE", "hypophosphatemia, autosomal recessive", "Hypophosphatemia, Autosomal Recessive", "Autosomal hypophosphatemic bone disease", "Autosomal hypophosphataemic bone disease", "Autosomal Recessive Hypophosphatemia Rickets", "Autosomal Recessive Hypophosphatemic Rickets", "Autosomal recessive hypophosphatemic rickets", "Autosomal recessive hypophosphataemic rickets", "HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL RECESSIVE, 1", "hypophosphatemic rickets, autosomal recessive, 1", "Hypophosphatemic Rickets, Autosomal Recessive, 1", "DMP1 autosomal recessive hypophosphatemic rickets", "hypophosphatemic rickets, autosomal recessive, type 1", "Autosomal recessive hypophosphatemic rickets (disorder)", "Autosomal recessive hypophosphatemic vitamin D refractory rickets", "Autosomal recessive hypophosphataemic vitamin D refractory rickets", "autosomal recessive hypophosphatemic rickets caused by mutation in DMP1", "Autosomal recessive hypophosphatemic vitamin D refractory rickets (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypophosphatemic rickets, autosomal recessive, 1", "shortest_name_length": 4}
{"curie": "MONDO:0008621", "names": ["UHS", "spun glass hair", "Spun-glass hair", "Spun glass hair", "cheveux incoiffables", "Cheveux incoiffables", "uncombable hair syndrome", "Uncombable hair syndrome", "UNCOMBABLE HAIR SYNDROME", "Unmanageable hair syndrome", "unmanageable hair syndrome", "PILI TRIANGULI ET CANALICULI", "pili trianguli et canaliculi", "Pili trianguli et canaliculi", "Pili trianguli et Canaliculi", "Uncombable hair syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uncombable hair syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0018599", "names": ["congenital CNIII lesion", "congenital oculomotor nerve palsy", "congenital third cranial nerve palsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital oculomotor nerve palsy", "shortest_name_length": 23}
{"curie": "MONDO:0011559", "names": ["BRIC2", "BRIC type 2", "Bric type 2", "mild ABCB11 deficiency", "benign recurrent intrahepatic cholestasis 2", "Cholestasis, benign recurrent intrahepatic 2", "cholestasis, benign recurrent intrahepatic 2", "cholestasis, benign recurrent intrahepatic, 2", "Cholestasis, Benign Recurrent Intrahepatic, 2", "recurrent familial intrahepatic cholestasis 2", "CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC, 2", "benign recurrent intrahepatic cholestasis type 2", "Benign recurrent intrahepatic cholestasis type 2", "Cholestasis, progressive familial intrahepatic 2", "cholestasis, benign recurrent intrahepatic, type 2", "Benign recurrent intrahepatic cholestasis 2 (BRIC2)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign recurrent intrahepatic cholestasis type 2", "shortest_name_length": 5}
{"curie": "MONDO:0030017", "names": ["COXPD43", "combined oxidative phosphorylation deficiency 43", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 43"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation deficiency 43", "shortest_name_length": 7}
{"curie": "UMLS:C1336190", "names": ["Stage IIB Non-Small Cell Lung Cancer", "stage IIB non-small cell lung cancer", "Stage IIB Non-Oat Cell Lung Carcinoma", "Stage IIB Non-Small Cell Lung Carcinoma", "Stage IIB Non-Oat Cell Carcinoma of Lung", "Stage IIB Non-Small Cell Carcinoma of Lung", "Stage IIB Non-Oat Cell Carcinoma of the Lung", "Stage IIB Non-Small Cell Carcinoma of the Lung", "Stage IIB Lung Non-Small Cell Carcinoma AJCC v7", "Stage IIB Non-Small Cell Lung Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Non-Small Cell Lung Carcinoma AJCC v7", "shortest_name_length": 36}
{"curie": "MONDO:0018436", "names": ["megakaryoblastic AML with t(1;22)(p13;q13)", "Megakaryoblastic AML with t(1;22)(p13;q13)", "megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13)", "Megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13)", "Megakaryoblastic acute myeloid leukaemia with t(1;22)(p13;q13)", "Megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13) (disorder)", "Megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13) (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13)", "shortest_name_length": 42}
{"curie": "MONDO:0014359", "names": ["PPNAD4", "chromosome 19P13 Duplication syndrome", "CHROMOSOME 19p13 DUPLICATION SYNDROME", "Cushing syndrome, adrenal, due to Ppnad4", "CUSHING SYNDROME, ADRENAL, DUE TO PPNAD4", "ACTH-INDEPENDENT ADRENAL CUSHING SYNDROME, SOMATIC", "ACTH-independent adrenal Cushing syndrome, somatic", "CUSHING SYNDROME, ACTH-INDEPENDENT ADRENAL, SOMATIC", "Cushing syndrome, ACTH-independent adrenal, somatic", "pigmented nodular adrenocortical disease, primary, 4", "PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4", "PRKACA primary pigmented nodular adrenocortical disease", "pigmented nodular adrenocortical disease, primary, type 4", "primary pigmented nodular adrenocortical disease caused by mutation in PRKACA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pigmented nodular adrenocortical disease, primary, 4", "shortest_name_length": 6}
{"curie": "MONDO:0011861", "names": ["Bhs", "BHS", "Breath Holding", "Breath-holding spell", "Breath Holding Spell", "Breath-holding Spell", "breath holding spell", "Breath holding spell", "BREATH-HOLDING SPELLS", "Breath holding spells", "holding breath spells", "breath-holding Spells", "Breath holding attack", "breath holding spells", "Breath-holding spells", "Breath-holding (spells)", "Breath holding spell (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breath-holding Spells", "shortest_name_length": 3}
{"curie": "UMLS:C0576995", "names": ["throat bleed", "bleeds throat", "throat bleeding", "bleeding throat", "PHARYNGEAL BLEED", "bleeding throats", "hemorrhage; throat", "throat; hemorrhage", "PHARYNGEAL BLEEDING", "Pharyngeal bleeding", "Bleeding of pharynx", "bleeding of pharynx", "bleeding from throat", "Bleeding from throat", "Pharyngeal Hemorrhage", "Pharyngeal hemorrhage", "HEMORRHAGE PHARYNGEAL", "Hemorrhage pharyngeal", "HAEMORRHAGE PHARYNGEAL", "Pharyngeal haemorrhage", "Haemorrhage pharyngeal", "Hemorrhage from throat", "hemorrhage from throat", "Hemorrhage from pharynx", "Haemorrhage from throat", "Haemorrhage from pharynx", "Bleeding of pharynx (finding)", "Pharyngeal hemorrhage (disorder)", "Observation of bleeding of pharynx", "bleeding of pharynx (physical finding)", "hemorrhage from throat (physical finding)", "respiratory passages hemorrhage from throat"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pharyngeal Hemorrhage", "shortest_name_length": 12}
{"curie": "MONDO:0002626", "names": ["Accessory Nerve Neoplasm", "accessory nerve neoplasm", "XIth cranial nerve tumors", "XIth Cranial nerve tumors", "XIth Cranial Nerve Tumors", "neoplasm of accessory nerve", "Neoplasm of accessory nerve", "Spinal Accessory Nerve Tumor", "XIth Cranial Nerve Neoplasms", "spinal accessory nerve tumor", "eleventh cranial nerve tumor", "Eleventh Cranial Nerve Tumor", "XIth cranial nerve neoplasms", "spinal accessory nerve tumors", "Eleventh Cranial Nerve Tumors", "Spinal Accessory Nerve Tumors", "eleventh cranial nerve tumors", "Tumor of Eleventh Cranial Nerve", "tumor of eleventh cranial nerve", "Tumor of Spinal Accessory Nerve", "tumor of spinal accessory nerve", "eleventh cranial nerve neoplasm", "spinal accessory nerve neoplasm", "Spinal Accessory Nerve Neoplasm", "Eleventh Cranial Nerve Neoplasm", "Eleventh Cranial Nerve Neoplasms", "spinal accessory nerve neoplasms", "eleventh cranial nerve neoplasms", "Spinal Accessory Nerve Neoplasms", "neoplasm of eleventh cranial nerve", "Neoplasm of Eleventh Cranial Nerve", "Neoplasm of Spinal Accessory Nerve", "neoplasm of spinal accessory nerve", "tumor of the spinal accessory nerve", "tumor of the eleventh cranial nerve", "Tumor of the Spinal Accessory Nerve", "Tumor of the Eleventh Cranial Nerve", "neoplasm of the eleventh cranial nerve", "neoplasm of the spinal accessory nerve", "Neoplasm of the Spinal Accessory Nerve", "Neoplasm of the Eleventh Cranial Nerve", "Neoplasm of accessory nerve (disorder)", "accessory XI nerve spinal component tumor", "tumor of accessory XI nerve spinal component", "accessory XI nerve spinal component neoplasm", "neoplasm of eleventh cranial nerve (diagnosis)", "neoplasm of accessory XI nerve spinal component", "accessory XI nerve spinal component neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal accessory nerve neoplasm", "shortest_name_length": 24}
{"curie": "UMLS:C1541468", "names": ["Grade III Lymphomatoid Granulomatosis", "Adult Grade III Lymphomatoid Granulomatosis", "adult grade III lymphomatoid granulomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Grade III Lymphomatoid Granulomatosis", "shortest_name_length": 37}
{"curie": "MONDO:0006939", "names": ["pyometrium", "PYELONEPHRITIS", "Pyelonephritis", "pyelonephritis", "Kidney Infection", "kidney infection", "Kidney infection", "Pyelonephritides", "Pyelonephritis NOS", "Pyelonephritis, NOS", "Pyelonephritis (disorder)", "pyelonephritis (diagnosis)", "Pyelonephritis, unspecified", "bacterial infection of the kidney"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyelonephritis", "shortest_name_length": 10}
{"curie": "UMLS:C5418564", "names": ["Metastatic Pancreatobiliary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Pancreatobiliary Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0035561", "names": ["sporadic human prion disease", "idiopathic human prion disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sporadic human prion disease", "shortest_name_length": 28}
{"curie": "MONDO:0014498", "names": ["FCAS4", "NLRC4-related familial cold urticaria", "familial cold autoinflammatory syndrome 4", "FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 4", "Familial cold autoinflammatory syndrome 4", "NLRC4 familial cold autoinflammatory syndrome", "familial cold autoinflammatory syndrome type 4", "NLRC4-related familial cold autoinflammatory syndrome", "familial cold autoinflammatory syndrome caused by mutation in NLRC4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial cold autoinflammatory syndrome 4", "shortest_name_length": 5}
{"curie": "MONDO:0000553", "names": ["uterine corpus endometrial carcinoma", "body of uterus endometrial carcinoma (disease)", "endometrial carcinoma (disease) of body of uterus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine corpus endometrial carcinoma", "shortest_name_length": 36}
{"curie": "UMLS:C1336131", "names": ["Stage IB Bone Sarcoma", "Stage IB Sarcoma of Bone", "Stage IB Sarcoma of the Bone", "Stage IB Bone Sarcoma AJCC v7", "Stage IB Bone Sarcoma  AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Bone Sarcoma AJCC v7", "shortest_name_length": 21}
{"curie": "MONDO:0018767", "names": ["TMAU", "TMAuria", "trimethylaminuria", "fish-odor syndrome", "fish odor syndrome", "stale fish syndrome", "fish malodor syndrome", "severe primary trimethylaminuria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe primary trimethylaminuria", "shortest_name_length": 4}
{"curie": "UMLS:C0751268", "names": ["Juvenile Leigh Disease", "Leigh Disease, Juvenile", "Juvenile Subacute Necrotizing Encephalopathy", "Subacute Necrotizing Encephalopathy, Juvenile", "Encephalopathy, Subacute Necrotizing, Juvenile"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Encephalopathy, Subacute Necrotizing, Juvenile", "shortest_name_length": 22}
{"curie": "MONDO:0009161", "names": ["aEDS", "dEDS", "EDS7C", "EDS 7C", "EDS VII", "EDSDERMS", "EDS VIIC", "DERMATOSPARAXIS", "Dermatosparaxis", "dermatosparaxis", "Arthrochalasia EDS", "dermatosparaxis EDS", "Dermatosparaxis EDS", "Ehlers-Danlos syndrome type 7", "Human dermatosparaxis EDS VIIC", "Ehlers-Danlos syndrome type 7C", "Procollagen protease deficiency", "Ehlers-Danlos syndrome type VII", "type VII Ehlers-Danlos syndrome", "Procollagen peptidase deficiency", "Ehlers-Danlos Syndrome, Type VII", "Ehlers-Danlos syndrome, type VII", "Arthrochalasis multiplex congenita", "Arthrochalasia multiplex congenita", "Procollagen aminoprotease deficiency", "Arthrochalasia Ehlers-Danlos syndrome", "dermatosparaxis Ehlers-Danlos syndrome", "Dermatosparaxis Ehlers-Danlos syndrome", "Ehlers-Danlos syndrome type 7C (formerly)", "Ehlers-Danlos syndrome dermatosparaxis type", "Ehlers-Danlos syndrome, arthrochalasia type", "EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE", "EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE", "Ehlers-Danlos Syndrome, Dermatosparaxis Type", "Ehlers-Danlos syndrome, dermatosparaxis type", "Dermatosparaxis EDS (Ehlers-Danlos syndrome)", "Ehlers-Danlos syndrome, type VII (diagnosis)", "Dermatosparaxis Ehlers-Danlos syndrome (disorder)", "Ehlers-Danlos syndrome, autosomal recessive type 7", "Ehlers-Danlos Syndrome, Type VII, Autosomal Recessive", "EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE", "Ehlers-Danlos syndrome, type VII, autosomal recessive", "Ehlers-Danlos syndrome, procollagen proteinase deficient", "Human dermatosparaxis EDS VIIC (Ehlers-Danlos syndrome type 7C)", "Cutis hyperelastica VII, arthrochalasis multiplex congenita type", "Ehlers-Danlos syndrome, procollagen proteinase deficient (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ehlers-Danlos syndrome, dermatosparaxis type", "shortest_name_length": 4}
{"curie": "MONDO:0021368", "names": ["major salivary gland tumor", "Major Salivary Gland Tumor", "major salivary gland neoplasm", "Tumor of Major Salivary Gland", "tumor of Major salivary gland", "Tumor of major salivary gland", "Major Salivary Gland Neoplasm", "tumor of major salivary gland", "Tumour of major salivary gland", "neoplasm of major salivary gland", "Neoplasm of major salivary gland", "Neoplasm of Major Salivary Gland", "Tumor of the Major Salivary Gland", "tumor of the Major salivary gland", "neoplasm of the Major salivary gland", "Neoplasm of the Major Salivary Gland", "major salivary gland neoplasm (disease)", "Neoplasm of major salivary gland (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplasm of major salivary gland", "shortest_name_length": 26}
{"curie": "UMLS:C5554918", "names": ["Refractory Extracranial Malignant Solid Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Extracranial Malignant Solid Neoplasm", "shortest_name_length": 48}
{"curie": "UMLS:C0586364", "names": ["PanIN-2", "Moderate pancreatic duct dysplasia", "Pancreatic Intraepithelial Neoplasia-2", "Grade 2 Pancreatic Intraepithelial Neoplasia", "Grade II Pancreatic Intraepithelial Neoplasia", "Moderate pancreatic duct dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Moderate pancreatic duct dysplasia", "shortest_name_length": 7}
{"curie": "MONDO:0021230", "names": ["cervix", "cervix tumor", "Cervix Tumor", "Cervical Tumor", "cervical tumor", "tumor of cervix", "Tumor of Cervix", "cervix neoplasm", "Cervix Neoplasm", "Cervical Neoplasm", "Cervical neoplasm", "neoplasm of cervix", "Neoplasm of Cervix", "Cervix Uteri Tumor", "cervix uteri tumor", "tumor of the cervix", "Tumor of the Cervix", "uterine cervix tumor", "Uterine Cervix Tumor", "Cervix Uteri Neoplasm", "cervix uteri neoplasm", "Tumor of Cervix Uteri", "tumor of cervix uteri", "neoplasm of the cervix", "Neoplasm of the Cervix", "uterine cervix neoplasm", "tumor of uterine cervix", "Tumor of Uterine Cervix", "Uterine Cervix Neoplasm", "Neoplasm of Cervix Uteri", "neoplasm of cervix uteri", "tumor of the cervix uteri", "Tumor of the Cervix Uteri", "Neoplasm of Uterine Cervix", "neoplasm of uterine cervix", "Tumor of the Uterine Cervix", "tumor of the uterine cervix", "Neoplasm of the Cervix Uteri", "neoplasm of the cervix uteri", "neoplasm of the uterine cervix", "Neoplasm of the Uterine Cervix", "uterine cervix neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine cervix neoplasm", "shortest_name_length": 6}
{"curie": "MONDO:0013849", "names": ["MCPH8", "primary autosomal recessive microcephaly 8", "MICROCEPHALY 8, PRIMARY, AUTOSOMAL RECESSIVE", "microcephaly 8, primary, autosomal recessive", "CEP135 autosomal recessive primary microcephaly", "autosomal recessive primary microcephaly caused by mutation in CEP135"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly 8, primary, autosomal recessive", "shortest_name_length": 5}
{"curie": "MONDO:0004040", "names": ["Bladder Inverted Papilloma", "bladder inverted papilloma", "urinary bladder inverted papilloma", "Urinary Bladder Inverted Papilloma", "Inverted papilloma of urinary bladder", "Inverted papilloma of urinary bladder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urinary bladder inverted papilloma", "shortest_name_length": 26}
{"curie": "MONDO:0008823", "names": ["AMCN", "AMC2", "AMC neurogenic type", "AMC, NEUROGENIC TYPE", "AMC, neurogenic type", "neurogenic type of AMC", "Neurogenic type of AMC", "neurogenic arthrogryposis multiplex congenita", "Neurogenic arthrogryposis multiplex congenita", "arthrogryposis multiplex congenita neurogenic type", "Arthrogryposis multiplex congenita neurogenic type", "Arthrogryposis Multiplex Congenita, Neurogenic Type", "arthrogryposis multiplex congenita, neurogenic type", "ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC TYPE", "neurogenic-type arthrogryposis multiplex congenita-2", "arthrogryposis multiplex congenita 2, neurogenic type", "ARTHROGRYPOSIS MULTIPLEX CONGENITA 2, NEUROGENIC TYPE", "Neurogenic arthrogryposis multiplex congenita (disorder)", "ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC TYPE (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis multiplex congenita 2, neurogenic type", "shortest_name_length": 4}
{"curie": "UMLS:C1336384", "names": ["Stage IVB Mouth Epidermoid Carcinoma", "Stage IVB Mouth Squamous Cell Carcinoma", "Stage IVB Epidermoid Carcinoma of Mouth", "Stage IVB Oral Cavity Epidermoid Carcinoma", "Stage IVB Oral Cavity Squamous Cell Cancer", "Stage IVB Squamous Cell Carcinoma of Mouth", "Stage IVB Epidermoid Carcinoma of the Mouth", "Stage IVB Epidermoid Carcinoma of Oral Cavity", "Stage IVB Oral Cavity Squamous Cell Carcinoma", "Stage IVB Squamous Cell Carcinoma of the Mouth", "Stage IVB Squamous Cell Carcinoma of Oral Cavity", "Stage IVB Epidermoid Carcinoma of the Oral Cavity", "Stage IVB Squamous Cell Carcinoma of the Oral Cavity", "Stage IVB Oral Cavity Squamous Cell Carcinoma AJCC v6", "Stage IVB Oral Cavity Squamous Cell Carcinoma AJCC v7", "Stage IVB Oral Cavity Squamous Cell Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Oral Cavity Squamous Cell Carcinoma AJCC v6 and v7", "shortest_name_length": 36}
{"curie": "MONDO:0011717", "names": ["HHF6", "hi/HA syndrome", "HA/hi syndrome", "HI/HA syndrome", "GDH hyperinsulinism", "GDH Hyperinsulinism", "GLUD1 hyperinsulinism", "GLUD1 Hyperinsulinism", "hyperinsulinism-hyperammonemia syndrome", "hyperinsulinism/hyperammonemia syndrome", "Hyperinsulinism/hyperammonemia syndrome", "Hyperinsulinism-hyperammonemia syndrome", "HYPERINSULINISM-HYPERAMMONEMIA SYNDROME", "Hyperinsulinism/Hyperammonemia Syndrome", "hyperinsulinism hyperammonemia syndrome", "familial hyperinsulinemic hypoglycemia 6", "hyperinsulinemic hypoglycemia familial 6", "Hyperinsulinism/hyperammonaemia syndrome", "glutamate dehydrogenase 1 hyperinsulinism", "Glutamate Dehydrogenase 1 Hyperinsulinism", "hyperinsulinemic hypoglycemia, familial, 6", "Hyperinsulinemic hypoglycemia, familial, 6", "HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 6", "Hyperinsulinism and hyperammonemia syndrome", "Hyperinsulinism and hyperammonaemia syndrome", "hyperinsulinemic hypoglycemia, familial, type 6", "Hyperinsulinism and hyperammonemia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperinsulinism-hyperammonemia syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0234247", "names": ["Atypical neuralgia", "neuralgia atypical", "atypical neuralgia", "Atypical Neuralgia", "Atypical Neuralgias", "Neuralgia, Atypical", "Neuralgia, atypical", "Neuralgias, Atypical", "Atypical neuralgia (finding)", "Atypical neuralgia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neuralgia, Atypical", "shortest_name_length": 18}
{"curie": "MONDO:0030329", "names": ["MMIHS5", "megacystis-microcolon-intestinal hypoperistalsis syndrome 5", "MEGACYSTIS-MICROCOLON-INTESTINAL HYPOPERISTALSIS SYNDROME 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "megacystis-microcolon-intestinal hypoperistalsis syndrome 5", "shortest_name_length": 6}
{"curie": "MONDO:0012542", "names": ["PSORS8", "psoriasis 8", "PSORIASIS SUSCEPTIBILITY 8", "psoriasis susceptibility 8", "psoriasis 8, susceptibility to", "PSORIASIS 8, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "psoriasis 8, susceptibility to", "shortest_name_length": 6}
{"curie": "MONDO:0024469", "names": ["cartilage cancer", "Tumor of Cartilage", "cartilage neoplasm", "tumor of cartilage", "Chondrogenic Tumor", "chondrogenic tumor", "Cartilage neoplasm", "Chondromatous Tumor", "chondromatous tumor", "Cartilaginous Tumor", "cartilaginous tumor", "neoplasm of cartilage", "Chondrogenic Neoplasm", "chondrogenic neoplasm", "Neoplasm of Cartilage", "Tumor of the Cartilage", "Chondromatous Neoplasm", "cartilaginous neoplasm", "chondromatous neoplasm", "Cartilage neoplasm NOS", "Cartilaginous Neoplasm", "tumor of the cartilage", "Chondromatous Neoplasms", "neoplasm of the cartilage", "Neoplasm of the Cartilage", "neoplasm of cartilage (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chondrogenic neoplasm", "shortest_name_length": 16}
{"curie": "MONDO:0016565", "names": ["syndromic genetic obesity", "syndromic obesity (disease)", "syndrome associated with obesity (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic genetic obesity", "shortest_name_length": 25}
{"curie": "MONDO:0006354", "names": ["parathyroid hyperplasia", "Parathyroid Hyperplasia", "Parathyroid hyperplasia", "PARATHYROID HYPERPLASIA", "parathyroid; hyperplasia", "hyperplasia; parathyroid", "Hyperplasia of parathyroid", "hyperplasia of parathyroid", "Hyperplasia of Parathyroid", "Enlarged parathyroid glands", "Parathyroid Gland Hyperplasia", "parathyroid gland hyperplasia", "hyperplasia of the parathyroid", "Hyperplasia of the Parathyroid", "parathyroid hyperplasia (disease)", "Parathyroid hyperplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parathyroid hyperplasia", "shortest_name_length": 23}
{"curie": "UMLS:C5555642", "names": ["Ovarian Leiomyoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Leiomyoma", "shortest_name_length": 17}
{"curie": "MONDO:0014703", "names": ["AOS6", "Adams-Oliver syndrome 6", "ADAMS-OLIVER SYNDROME 6", "DLL4 Adams-Oliver syndrome", "Adams-Oliver syndrome type 6", "Adams-Oliver syndrome caused by mutation in DLL4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adams-Oliver syndrome 6", "shortest_name_length": 4}
{"curie": "MONDO:0009470", "names": ["BRWS1", "COFLS", "Fryns-Aftimos syndrome", "FRYNS-AFTIMOS SYNDROME", "ACTB-related BAFopathy", "Fryns-Aftimos Syndrome", "Baraitser-Winter syndrome", "Baraitser-WINTER syndrome 1", "BARAITSER-WINTER SYNDROME 1", "Baraitser-Winter syndrome 1", "CEREBROFRONTOFACIAL SYNDROME", "cerebrofrontofacial syndrome", "Cerebrofrontofacial Syndrome", "Baraitser-Winter syndrome type 1", "CHROMOSOME 7p22 DELETION SYNDROME", "chromosome 7P22 deletion syndrome", "cerebrooculofacial lymphatic syndrome", "Cerebrooculofacial Lymphatic Syndrome", "CEREBROOCULOFACIAL LYMPHATIC SYNDROME", "ACTB Baraitser-Winter cerebrofrontofacial syndrome", "mental retardation with epilepsy and characteristic facies", "MENTAL RETARDATION WITH EPILEPSY AND CHARACTERISTIC FACIES", "Mental Retardation with Epilepsy and Characteristic Facies", "iris coloboma-ptosis-hypertelorism-mental retardation syndrome", "intellectual disability with epilepsy and characteristic facies", "Iris Coloboma with Ptosis, Hypertelorism, and Mental Retardation", "IRIS COLOBOMA WITH PTOSIS, HYPERTELORISM, AND MENTAL RETARDATION", "iris coloboma with ptosis, hypertelorism, and mental retardation", "PACHYGYRIA, MENTAL RETARDATION, EPILEPSY, AND CHARACTERISTIC FACIES", "Pachygyria, Mental Retardation, Epilepsy, and Characteristic Facies", "pachygyria, mental retardation, epilepsy, and characteristic facies", "iris coloboma with ptosis, hypertelorism, and intellectual disability", "Baraitser-Winter cerebrofrontofacial syndrome caused by mutation in ACTB", "pachygyria, intellectual disability, epilepsy, and characteristic facies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Baraitser-Winter syndrome 1", "shortest_name_length": 5}
{"curie": "MONDO:0008999", "names": ["COH", "Coh", "Chs1", "COH1", "Norio Syndrome", "cohen syndrome", "CHS1, FORMERLY", "Norio syndrome", "Cohen syndrome", "Chs1, formerly", "COHEN SYNDROME", "pepper syndrome", "Pepper syndrome", "PEPPER SYNDROME", "cohens syndrome", "cohen's syndrome", "Cohen's syndrome", "Cohen syndrome (disorder)", "obesity-hypotonia syndrome", "Obesity-Hypotonia Syndrome", "Hypotonia, Obesity, and Prominent Incisors", "Hypotonia, obesity, and prominent incisors", "hypotonia, obesity, and prominent incisors", "HYPOTONIA, OBESITY, AND PROMINENT INCISORS", "Prominent Incisors-Obesity-Hypotonia Syndrome", "hypotonia-obesity-prominent incisors syndrome", "prominent incisors-obesity-hypotonia syndrome", "Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness", "cutis verticis gyrata, retinitis pigmentosa, and sensorineural deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cohen syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0010129", "names": ["thymic-renal-anal-lung dysplasia", "THYMIC-RENAL-ANAL-LUNG DYSPLASIA", "Thymic-Renal-Anal-Lung dysplasia", "Thymic-renal-anal-lung dysplasia", "Thymic, renal, anal, lung dysplasia syndrome", "Thymic, renal, anal, lung dysplasia syndrome (disorder)", "syndrome of unilobed or absent thymus, renal and ureter agenesis/dysgenesis, and intrauterine growth retardation (IUGR)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thymic-renal-anal-lung dysplasia", "shortest_name_length": 32}
{"curie": "UMLS:C1619727", "names": ["cirrhosis decompensated", "Decompensated cirrhosis", "Decompensated cirrhosis of liver", "Decompensated cirrhosis (diagnosis)", "Decompensated cirrhosis of liver (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Decompensated cirrhosis of liver", "shortest_name_length": 23}
{"curie": "MONDO:0018311", "names": ["acromelanosis", "Acromelanosis", "Acromelanosis (disorder)", "progressive acromelanosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acromelanosis", "shortest_name_length": 13}
{"curie": "UMLS:C0848450", "names": ["Carcinoma Unspecified Site", "Carcinoma, unspecified site", "carcinoma site not specified", "Carcinoma;site not specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carcinoma Unspecified Site", "shortest_name_length": 26}
{"curie": "MONDO:0044915", "names": ["Salivary duct carcinoma", "Salivary Duct Carcinoma", "salivary duct carcinoma", "Carcinoma of Salivary Duct", "carcinoma of salivary duct", "Carcinoma of the Salivary Duct", "carcinoma of the salivary duct", "duct of salivary gland carcinoma", "high grade salivary duct carcinoma", "High Grade Salivary Duct Carcinoma", "carcinoma of duct of salivary gland", "Salivary duct carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "salivary duct carcinoma", "shortest_name_length": 23}
{"curie": "MONDO:0014681", "names": ["NMTC4", "thyroid cancer, nonmedullary, 4", "THYROID CANCER, NONMEDULLARY, 4", "FOXE1 thyroid cancer, nonmedullary", "thyroid cancer, nonmedullary, type 4", "thyroid cancer, nonmedullary caused by mutation in FOXE1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid cancer, nonmedullary, 4", "shortest_name_length": 5}
{"curie": "UMLS:C0812470", "names": ["Abortion incomplete", "abortion incomplete", "Incomplete Abortion", "Abortion;incomplete", "Incomplete abortion", "incomplete abortion", "Abortion, incomplete", "ABORTION, INCOMPLETE", "incomplete abortions", "Abortion incomplete NOS", "Incomplete Induced Abortion", "incomplete abortion (diagnosis)", "Unspecified abortion incomplete"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unspecified abortion incomplete", "shortest_name_length": 19}
{"curie": "MONDO:0020793", "names": ["OPDM1", "oculopharyngodistal myopathy", "oculopharyngodistal myopathy 1", "OCULOPHARYNGODISTAL MYOPATHY 1", "faciooculolaryngopharyngeal myopathy with distal and respiratory involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculopharyngodistal myopathy 1", "shortest_name_length": 5}
{"curie": "MONDO:0007541", "names": ["ENDO1", "endometriosis, susceptibility to, 1", "ENDOMETRIOSIS, SUSCEPTIBILITY TO, 1", "endometriosis, susceptibility to, type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometriosis, susceptibility to, 1", "shortest_name_length": 5}
{"curie": "MONDO:0022407", "names": ["retinal ciliopathy due to mutation in Bardet-Biedl gene"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal ciliopathy due to mutation in Bardet-Biedl gene", "shortest_name_length": 55}
{"curie": "MONDO:0010667", "names": ["PRS", "MRXS2", "Prieto syndrome", "PRIETO SYNDROME", "Prieto syndrome (PRS)", "Prieto-Badia-Mulas syndrome", "Prieto Badia Mulas syndrome", "Prieto syndrome, X-linked recessive", "X-linked mental retardation syndrome 2", "MENTAL RETARDATION, X-LINKED, SYNDROMIC 2", "Mental retardation, X-linked, syndromic 2", "mental retardation, X-linked, syndromic 2", "Prieto X-linked mental retardation syndrome", "PRIETO X-LINKED MENTAL RETARDATION SYNDROME", "X-linked mental retardation syndrome 2 (MRXS2)", "intellectual disability, X-linked, syndromic 2", "Prieto X-linked intellectual disability syndrome", "X-linked dysmorphic syndrome with mental retardation", "mental retardation-dysmorphism-cerebral atrophy syndrome", "Mental retardation, X-linked with dysmorphism and cerebral atrophy", "MENTAL RETARDATION, X-LINKED, WITH DYSMORPHISM AND CEREBRAL ATROPHY", "mental retardation, X-linked, with Dysmorphism and cerebral atrophy", "Mental Retardation, X-Linked, With Dysmorphism And Cerebral Atrophy", "X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome", "intellectual disability, X-linked, with Dysmorphism and cerebral atrophy", "x-linked intellectual disability w/ dysmorphism & cerebral atrophy syndrome", "X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome", "X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder)", "X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prieto syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0013377", "names": ["MCOP7", "isolated microphthalmia 7", "MICROPHTHALMIA, ISOLATED 7", "microphthalmia, isolated 7", "GDF3 isolated microphthalmia", "isolated microphthalmia type 7", "microphthalmia, isolated type 7", "isolated microphthalmia caused by mutation in GDF3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated microphthalmia 7", "shortest_name_length": 5}
{"curie": "MONDO:0009179", "names": ["RDEB", "EBR1", "EBD inversa", "RDEB-sev gen", "severe generalized RDEB", "RDEB, severe generalized", "RDEB generalisata gravis", "Hallopeau Siemens Disease", "Hallopeau-Siemens Disease", "RDEB, Hallopeau-Siemens type", "Polydysplastic epidermolysis bullosa", "polydysplastic epidermolysis bullosa", "epidermolysis bullosa dystrophica, AR", "Dermolytic bullous dermatosis, recessive", "Recessive dystrophic epidermolysis bullosa", "recessive dystrophic epidermolysis bullosa", "Recessive Dystrophic Epidermolysis Bullosa", "Epidermolysis Bullosa Dystrophica, Recessive", "Dysplastic epidermolysis bullosa dystrophica", "Epidermolysis bullosa dystrophica, recessive", "polydysplastic epidermolysis bullosa (diagnosis)", "dystrophic epidermolysis bullosa, autosomal recessive", "DYSTROPHIC EPIDERMOLYSIS BULLOSA, AUTOSOMAL RECESSIVE", "Recessive dystrophic epidermolysis bullosa (disorder)", "Dystrophic Epidermolysis Bullosa, Autosomal Recessive", "epidermolysis bullosa dystrophica, autosomal recessive", "Epidermolysis Bullosa Dystrophica, Autosomal Recessive", "EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE", "Epidermolysis Bullosa Dystrophica, Hallopeau Siemens Type", "epidermolysis bullosa dystrophica, Hallopeau-Siemens type", "EPIDERMOLYSIS BULLOSA DYSTROPHICA, HALLOPEAU-SIEMENS TYPE", "Epidermolysis Bullosa Dystrophica, Hallopeau-Siemens Type", "severe generalized recessive dystrophic epidermolysis bullosa", "epidermolysis bullosa dystrophica inversa, autosomal recessive", "recessive dystrophic epidermolysis bullosa, severe generalized", "Epidermolysis Bullosa Dystrophica Inversa, Autosomal Recessive", "EPIDERMOLYSIS BULLOSA DYSTROPHICA INVERSA, AUTOSOMAL RECESSIVE", "epidermolysis bullosa dystrophica, autosomal recessive, modifier of", "autosomal recessive dystrophic epidermolysis bullosa generalisata gravis", "epidermolysis bullosa dystrophica, generalized severe, autosomal recessive", "EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE, LOCALISATA VARIANT", "epidermolysis bullosa dystrophica, autosomal recessive, Localisata variant", "EPIDERMOLYSIS BULLOSA DYSTROPHICA, GENERALIZED SEVERE, AUTOSOMAL RECESSIVE", "Epidermolysis Bullosa Dystrophica, Autosomal Recessive, Localisata Variant", "autosomal recessive dystrophic epidermolysis bullosa, Hallopeau-Siemens type", "autosomal recessive dystrophic epidermolysis bullosa, Hallopeau-Siemens type (formerly)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "recessive dystrophic epidermolysis bullosa", "shortest_name_length": 4}
{"curie": "UMLS:C0268732", "names": ["nephritic syndrome", "Nephritic Syndrome", "Nephritic syndrome", "syndrome nephritic", "nephritic; syndrome", "syndrome; nephritic", "nephritic syndromes", "Nephritic syndrome, NOS", "Nephritic syndrome (disorder)", "nephritic syndrome (diagnosis)", "Unspecified nephritic syndrome", "Unspecified nephritic syndrome, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephritic syndrome", "shortest_name_length": 18}
{"curie": "UMLS:C0852720", "names": ["Visual acuity reduced transiently", "Deterioration of visual acuity temporarily"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Visual acuity reduced transiently", "shortest_name_length": 33}
{"curie": "OMIM:607676", "names": ["IPD", "IMD67", "IRAK4D", "IKAK4D", "IRAK4 Deficiency", "IRAK4 deficiency", "IRAK4 DEFICIENCY", "Irak-4 Deficiency", "IMMUNODEFICIENCY 67", "INVASIVE PNEUMOCOCCAL DISEASE, PROTECTION AGAINST", "INVASIVE PNEUMOCOCCAL DISEASE, RECURRENT ISOLATED", "Invasive Pneumococcal Disease, Recurrent Isolated, 1", "Immunodeficiency due to interleukin-1 receptor-associated kinase-4 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 3}
{"curie": "UMLS:C4289043", "names": ["Gemistocytic Astrocytoma, IDH Mutant", "Gemistocytic Astrocytoma, IDH-Mutant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gemistocytic Astrocytoma, IDH-Mutant", "shortest_name_length": 36}
{"curie": "MONDO:0006796", "names": ["Hypertensive Encephalopathy", "ENCEPHALOPATHY HYPERTENSIVE", "Encephalopathy hypertensive", "HYPERTENSIVE ENCEPHALOPATHY", "Hypertensive encephalopathy", "encephalopathy hypertensive", "hypertensive encephalopathy", "ENCEPHALOPATHY, HYPERTENSIVE", "encephalopathy; hypertensive", "Encephalopathy, Hypertensive", "Hypertensive encephalopathy syndrome", "Hypertensive encephalopathy (disorder)", "hypertensive encephalopathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertensive encephalopathy", "shortest_name_length": 27}
{"curie": "UMLS:C1537102", "names": ["Sinonasal Inverted Papilloma", "Inverted Schneiderian Papilloma", "Schneiderian papilloma, inverted", "Sinonasal Inverted Schneiderian Papilloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Inverted Papilloma", "shortest_name_length": 28}
{"curie": "MONDO:0017161", "names": ["FTDALS", "FTD-ALS", "FTD-MND", "frontotemporal dementia with ALS", "Frontotemporal Dementia With Motor Neuron Disease", "frontotemporal dementia with motor neuron disease", "frontotemporal dementia with amyotrophic lateral sclerosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontotemporal dementia with motor neuron disease", "shortest_name_length": 6}
{"curie": "MONDO:0008016", "names": ["DA7", "Hecht syndrome", "HECHT SYNDROME", "Hecht-Beals syndrome", "Dutch-Kentucky syndrome", "Hecht syndrome (disorder)", "Trismus-pseudocamptodactyly", "Distal arthrogryposis type 7", "distal arthrogryposis type 7", "arthrogryposis distal type 7", "Arthrogryposis, Distal, Type 7", "arthrogryposis, distal, type 7", "ARTHROGRYPOSIS, DISTAL, TYPE 7", "Trismus-pseudocamptodactyly syndrome", "TRISMUS-PSEUDOCAMPTODACTYLY SYNDROME", "trismus-pseudocamptodactyly syndrome", "Trismus-Pseudocamptodactyly Syndrome", "Trismus pseudocamptodactyly syndrome", "arthrogryposis distal type 7 (diagnosis)", "mouth, inability to open completely, and short finger-flexor tendons", "MOUTH, INABILITY TO OPEN COMPLETELY, AND SHORT FINGER-FLEXOR TENDONS", "mouth, inability to completely open, and short finger-flexor tendons"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trismus-pseudocamptodactyly syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0002318", "names": ["tracheal tumor", "trachea neoplasm", "trachea leiomyoma", "Trachea Leiomyoma", "tracheal neoplasm", "tracheal leiomyoma", "Tracheal Leiomyoma", "Leiomyoma of Trachea", "leiomyoma of trachea", "leiomyoma of the Trachea", "Leiomyoma of the Trachea", "leiomyoma of the trachea", "leiomyoma of trachea (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trachea leiomyoma", "shortest_name_length": 14}
{"curie": "MONDO:0001398", "names": ["ureteral tumor", "neoplasm of ureter", "Benign Ureter Tumor", "benign ureter tumor", "benign ureteral tumor", "Benign Ureteral Tumor", "Benign Tumor of Ureter", "benign tumor of ureter", "Benign tumor of ureter", "ureter benign neoplasm", "benign ureter neoplasm", "Benign Ureter Neoplasm", "Neoplasm benign;ureter", "Benign tumour of ureter", "Benign Ureteric Neoplasm", "benign ureteric neoplasm", "ureteral benign neoplasm", "benign ureteral neoplasm", "Benign Ureteral Neoplasm", "benign neoplasm of ureter", "Benign neoplasm of ureter", "Benign Neoplasm of Ureter", "Benign Tumor of the Ureter", "benign tumor of the ureter", "Benign Ureteric Neoplasm NOS", "Benign ureteric neoplasm NOS", "Benign Neoplasm of the Ureter", "benign neoplasm of the ureter", "Benign neoplasm of ureter (disorder)", "benign neoplasm of ureter (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ureter benign neoplasm", "shortest_name_length": 14}
{"curie": "MONDO:0001231", "names": ["periostitis; orbit", "orbit; periostitis", "Orbital periostitis", "orbital periostitis", "Periostitis of orbit", "Orbital osteoperiostitis", "Orbital periostitis (disorder)", "orbital periostitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orbital periostitis", "shortest_name_length": 18}
{"curie": "UMLS:C4727427", "names": ["Recurrent Malignant Brain Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Malignant Brain Neoplasm", "shortest_name_length": 34}
{"curie": "UMLS:C1511090", "names": ["Uterine Corpus Metastasizing Leiomyoma", "Benign Metastasizing Leiomyoma of the Uterine Corpus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Corpus Metastasizing Leiomyoma", "shortest_name_length": 38}
{"curie": "UMLS:C1960100", "names": ["Shellfish Poisoning", "Shellfish poisoning", "Shellfish Poisonings", "Poisoning, Shellfish", "toxicity to shellfish", "Poisonings, Shellfish", "Shellfish toxic effect", "food toxicity to shellfish", "Toxic effect from eating shellfish", "food toxicity to shellfish (diagnosis)", "Toxic effect from eating shellfish, NOS", "Toxic effect from eating shellfish (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Shellfish Poisoning", "shortest_name_length": 19}
{"curie": "MONDO:0006607", "names": ["Other acne", "sebaceous gland disease", "Sebaceous Gland Disease", "Sebaceous gland disorder", "sebaceous gland disorder", "Sebaceous Gland Diseases", "SEBACEOUS GLAND DISORDER", "Disease, Sebaceous Gland", "Gland Disease, Sebaceous", "sebaceous gland disorders", "Sebaceous Gland Disorders", "Gland Diseases, Sebaceous", "Sebaceous gland disorders", "Diseases, Sebaceous Gland", "sebaceous glands; disease", "Sebaceous glands--Diseases", "disease of sebaceous gland", "disorders glands sebaceous", "Disorder of sebaceous gland", "disease of sebaceous glands", "disorder of sebaceous gland", "Disease of sebaceous glands", "Sebaceous gland disorder NOS", "Diseases of sebaceous glands", "Disease of sebaceous glands, NOS", "DISEASES OF THE SEBACEOUS GLANDS", "sebaceous gland disease or disorder", "Disorder of sebaceous gland (disorder)", "disease or disorder of sebaceous gland", "disorder of sebaceous gland (diagnosis)", "disease (or disorder); sebaceous glands", "Unspecified disease of sebaceous glands"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sebaceous gland disorder", "shortest_name_length": 10}
{"curie": "UMLS:C2347915", "names": ["Recurrent Grade III Lymphomatoid Granulomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Grade III Lymphomatoid Granulomatosis", "shortest_name_length": 47}
{"curie": "MONDO:0000879", "names": ["skin thrush", "rash candida", "candida rash", "Candida rash", "candida skin", "skin candida", "Skin candida", "Monilial rash", "Candida of skin", "Moniliasis skin", "MONILIASIS SKIN", "Skin Candidiasis", "Skin candida NOS", "candidiasis skin", "skin; candidiasis", "candidiasis; skin", "Candidosis of skin", "Thrush of skin NOS", "Candidiasis of skin", "Monilia of skin NOS", "CANDIDIASIS OF SKIN", "CUTANEOUS MONILIASIS", "Moniliasis cutaneous", "Cutaneous moniliasis", "MONILIASIS CUTANEOUS", "cutaneous moniliasis", "Cutaneous candidiasis", "Moniliasis, Cutaneous", "MONILIASIS, CUTANEOUS", "cutaneous candidiasis", "Cutaneous Candidiasis", "candidiasis cutaneous", "candida skin infection", "CANDIDIASIS, CUTANEOUS", "SKIN INFECTION CANDIDA", "Candidiasis, Cutaneous", "Candidiasis of skin NOS", "candida infections skin", "zone of skin candidiasis", "Candidiasis of skin (disorder)", "SKIN INFECTION CANDIDA INFECTION", "cutaneous candidiasis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous candidiasis", "shortest_name_length": 11}
{"curie": "UMLS:C0280427", "names": ["relapsed adult T-Cell leukemia/lymphoma", "Adult T-Cell Lymphoma/Leukemia Recurrent", "Recurrent Adult T-Cell Lymphoma/Leukemia", "Adult T-cell lymphoma/leukemia recurrent", "adult T-cell leukemia/lymphoma, relapsed", "Recurrent Adult T-Cell Leukemia/Lymphoma", "recurrent adult T-cell leukemia/lymphoma", "adult T-cell leukemia/lymphoma, recurrent", "Adult T-cell lymphoma/leukaemia recurrent", "adult T-cell leukemia/lymphoma - in relapse", "adult T-cell leukemia/lymphoma - in relapse (diagnosis)", "Relapsed HTLV-1 Associated Adult T-Cell Lymphoma/Leukemia", "relapsed HTLV-I associated adult T-cell leukemia/lymphoma", "HTLV-1 Associated Adult T-Cell Lymphoma/Leukemia Relapsed", "HTLV-I associated adult T-cell leukemia/lymphoma, relapsed", "recurrent HTLV-I associated adult T-cell leukemia/lymphoma", "Recurrent HTLV-1 Associated Adult T-Cell Lymphoma/Leukemia", "HTLV-1 Associated Adult T-Cell Lymphoma/Leukemia Recurrent", "HTLV-I associated adult T-cell leukemia/lymphoma, recurrent", "Adult T-cell lymphoma/leukemia (HTLV-1-associated), in relapse"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult T-cell lymphoma/leukemia recurrent", "shortest_name_length": 39}
{"curie": "UMLS:C5555197", "names": ["Platinum-Refractory Primary Peritoneal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Platinum-Refractory Primary Peritoneal Carcinoma", "shortest_name_length": 48}
{"curie": "MONDO:0014131", "names": ["SHNS", "SHAHEEN syndrome", "Shaheen syndrome", "SHAHEEN SYNDROME", "hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome", "Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome", "Hypohidrosis, enamel hypoplasia, palmoplantar keratoderma, intellectual disability syndrome", "Hypohidrosis, enamel hypoplasia, palmoplantar keratoderma, intellectual disability syndrome (disorder)", "Hypohidrosis, enamel hypoplasia, palmoplantar keratoderma, intellectual disability syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C1558046", "names": ["Vas deferens perforation", "Vas Deferens Perforation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vas deferens perforation", "shortest_name_length": 24}
{"curie": "UMLS:C4682558", "names": ["Stage II Uterine Corpus Leiomyosarcoma", "Stage II Uterine Corpus Leiomyosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Uterine Corpus Leiomyosarcoma AJCC v8", "shortest_name_length": 38}
{"curie": "MONDO:0007130", "names": ["tapvd", "TAPVR", "tapvr", "TAPVR1", "Halasz syndrome", "scimitar anomaly", "scimitar syndrome", "hypogenetic lung syndrome", "mirror-image lung syndrome", "pulmonary venolobar syndrome", "congenital venolobar syndrome", "anomalous pulmonary Venous return", "vena cava bronchovascular syndrome", "Total Anomalous Pulmonary Venous Return", "total anomalous pulmonary venous return", "Total anomalous pulmonary venous return", "v.pulmonalis; anomaly connection, total", "Total anomalous pulmonary venous drainage", "TOTAL ANOMALOUS PULMONARY VENOUS DRAINAGE", "TOTAL ANOMALOUS PULMONARY VENOUS RETURN 1", "PULMONARY VENOUS RETURN, ANOMALOUS, TOTAL", "Total Anomalous Pulmonary Venous Return 1", "total anomalous pulmonary VENOUS return 1", "Total anomalous pulmonary venous connection", "connection; pulmonary veins, anomaly, total", "anomaly; connection, pulmonary veins, total", "anomaly; pulmonary, venous connection, total", "congenital total pulmonary venous return anomaly", "TAPVD - Total anomalous pulmonary venous drainage", "Total anomalous pulmonary venous return (disorder)", "total anomalous pulmonary venous return (diagnosis)", "TAPVC - Total anomalous pulmonary venous connection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital total pulmonary venous return anomaly", "shortest_name_length": 5}
{"curie": "MONDO:0017060", "names": ["Open iniencephaly", "open iniencephaly", "Iniencephaly - open", "Iniencephalus apertus", "Iniencephaly - open (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "open iniencephaly", "shortest_name_length": 17}
{"curie": "MONDO:0017129", "names": ["genetic heart tumor", "genetic cardiac tumor", "inherited cardiac tumor", "hereditary heart neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited cardiac tumor", "shortest_name_length": 19}
{"curie": "MONDO:0009744", "names": ["CLN1", "CLN1 disease", "congenital NCL", "Santavuori disease", "Santavuori Disease", "ceroid storage disease", "adult CLN (type of CLN1)", "Santavuori-Haltia disease", "CLN1 variable age at onset", "lipofuscin storage disease", "juvenile CLN (type of CLN1)", "infantile CLN (type of CLN1)", "neuronal ceroid lipofuscinosis 1", "ceroid lipofuscinosis neuronal 1", "CEROID LIPOFUSCINOSIS, NEURONAL, 1", "Ceroid Lipofuscinosis, Neuronal, 1", "ceroid lipofuscinosis, neuronal, 1", "PPT1 neuronal ceroid lipofuscinosis", "neuronal ceroid lipofuscinosis type 1", "Neuronal Ceroid Lipofuscinosis Type 1", "ceroid lipofuscinosis, neuronal, type 1", "infantile neuronal ceroid lipofuscinosis", "Infantile Neuronal Ceroid Lipofuscinosis", "classic late infantile CLN (type of CLN1)", "congenital neuronal ceroid lipofuscinosis", "neuronal ceroid lipofuscinosis, infantile", "neuronal ceroid lipofuscinosis 1 variable age of onset", "CEROID LIPOFUSCINOSIS, NEURONAL, 1, VARIABLE AGE AT ONSET", "neuronal ceroid lipofuscinosis caused by mutation in PPT1", "Ceroid Lipofuscinosis, Neuronal, 1, Variable Age at Onset", "ceroid lipofuscinosis, neuronal, 1, variable Age at onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuronal ceroid lipofuscinosis 1", "shortest_name_length": 4}
{"curie": "MONDO:0017668", "names": ["Stoll-Géraudel-Chauvin syndrome", "Stoll-GC)raudel-Chauvin syndrome", "mental retardation short stature hypertelorism", "intellectual disability short stature hypertelorism", "intellectual deficit - short stature - hypertelorism", "intellectual disability-short stature-hypertelorism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability-short stature-hypertelorism syndrome", "shortest_name_length": 31}
{"curie": "UMLS:C5555057", "names": ["Sarcoma with BCOR genetic alterations", "Sarcoma with BCOR Genetic Alterations", "Sarcoma with BCOR genetic alterations (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sarcoma with BCOR genetic alterations", "shortest_name_length": 37}
{"curie": "MONDO:0023046", "names": ["ectodermal dysplasia blindness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia blindness", "shortest_name_length": 30}
{"curie": "MONDO:0014629", "names": ["AILJK", "copa defect", "COPA syndrome", "copa syndrome", "COPA (coatomer protein complex subunit alpha) syndrome", "AUTOIMMUNE INTERSTITIAL LUNG, JOINT, AND KIDNEY DISEASE", "Autoimmune interstitial lung disease-arthritis syndrome", "autoimmune interstitial lung, joint, and kidney disease", "autoimmune interstitial lung disease-arthritis syndrome", "Autoimmune interstitial lung disease, arthritis syndrome", "Autoimmune interstitial lung disease, arthritis syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune interstitial lung disease-arthritis syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0018631", "names": ["MUHH", "MUHH1", "Hypt4", "HYPT4", "Muhh1", "HYPOTRICHOSIS 4", "Hypotrichosis 4", "hypotrichosis 4", "HR hypotrichosis", "Marie Unna syndrome", "hypotrichosis type 4", "hypotrichosis, Marie Unna type", "Hypotrichosis, Marie Unna type", "Marie Unna syndrome (disorder)", "hypotrichosis, Marie Unna type, 1", "HYPOTRICHOSIS, MARIE UNNA TYPE, 1", "Hypotrichosis, Marie Unna Type, 1", "Marie Unna congenital hypotrichosis", "Marie Unna hereditary hypotrichosis", "Hypotrichosis congenita hereditaria", "MARIE UNNA HEREDITARY HYPOTRICHOSIS 1", "Marie Unna Hereditary Hypotrichosis 1", "Marie Unna hereditary hypotrichosis 1", "hypotrichosis caused by mutation in HR"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Marie Unna hereditary hypotrichosis", "shortest_name_length": 4}
{"curie": "MONDO:0700068", "names": ["POMGNT1 myopathy", "POMGNT1-related myopathy", "myopathy caused by mutation in POMGNT1", "myopathy caused by variation in POMGNT1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy caused by variation in POMGNT1", "shortest_name_length": 16}
{"curie": "UMLS:C3854349", "names": ["Expulsion of medication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Expulsion of medication", "shortest_name_length": 23}
{"curie": "MONDO:0009902", "names": ["CEP", "Cep", "Günther disease", "UROS DEFICIENCY", "Uros deficiency", "UROS Deficiency", "Gunther disease", "GUNTHER DISEASE", "gunther disease", "Gunther Disease", "Gunthers Disease", "gunthers disease", "Gunther's Disease", "Gunther's disease", "gunther's disease", "cutaneous porphyria", "Congenital porphyria", "congenital porphyria", "Erythropoietic porphyria", "Erythropoietic Porphyria", "erythropoietic porphyria", "Erythropoietic Porphyrias", "Hematoporphyria congenita", "erythropoietic; porphyria", "Porphyria, erythropoietic", "Porphyria, Erythropoietic", "PORPHYRIA, ERYTHROPOIETIC", "porphyria; erythropoietic", "Porphyria erythropoietica", "Haematoporphyria congenita", "Porphyrias, Erythropoietic", "erythropoietic uroporphyria", "Erythropoietic uroporphyria", "UROPORPHYRIA, ERYTHROPOIETIC", "Erythropoietic porphyria, NOS", "erythropoietic porphyria (CEP)", "Congenital porphyria (disorder)", "congenital photosensitive porphyria", "Congenital photosensitive porphyria", "congenital erythropoietic porphyria", "Erythropoietic porphyria (disorder)", "Congenital Erythropoietic Porphyria", "Congenital erythropoietic porphyria", "Hereditary erythropoietic porphyria", "Porphyria, congenital erythropoietic", "Erythropoietic Porphyria, Congenital", "PORPHYRIA, CONGENITAL ERYTHROPOIETIC", "porphyria, congenital erythropoietic", "Porphyria, Congenital Erythropoietic", "Congenital Erythropoietic Porphyrias", "Porphyrias, Congenital Erythropoietic", "PORPHYRIA, PHOTOSENSITIVE, CONGENITAL", "Erythropoietic Porphyrias, Congenital", "Porphyria, Erythropoietic, Congenital", "PORPHYRIA, ERYTHROPOIETIC, CONGENITAL", "uroporphyrinogen 3 synthase deficiency", "UROPORPHYRINOGEN III SYNTHASE DEFICIENCY", "Uroporphyrinogen III synthase deficiency", "CEP - Congenital erythropoietic porphyria", "Deficiency of Uroporphyrinogen III Synthase", "uroporphyrinogen III synthase, deficiency of", "Uroporphyrinogen III Synthase, Deficiency of", "Congenital erythropoietic porphyria (disorder)", "congenital erythropoietic porphyria (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous porphyria", "shortest_name_length": 3}
{"curie": "UMLS:C0343770", "names": ["Bacillary peliosis", "Bacillary Pelioses", "Bacillary Peliosis", "Pelioses, Bacillary", "Peliosis, Bacillary", "Bacillary peliosis (diagnosis)", "Bacillary peliosis caused by Bartonella", "Bacillary peliosis caused by Bartonella (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bacillary Peliosis", "shortest_name_length": 18}
{"curie": "MONDO:0008648", "names": ["familial ventricular tachycardia", "Familial ventricular tachycardia", "ventricular tachycardia, familial", "VENTRICULAR TACHYCARDIA, FAMILIAL", "Ventricular Tachycardia, Familial", "hereditary ventricular tachycardia", "ventricular tachycardia, idiopathic", "Familial ventricular tachycardia (disorder)", "Familial polymorphic ventricular tachycardia", "Ventricular Tachycardia, Familial Polymorphic", "VENTRICULAR TACHYCARDIA, FAMILIAL POLYMORPHIC", "ventricular tachycardia, familial polymorphic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ventricular tachycardia, familial", "shortest_name_length": 32}
{"curie": "MONDO:0002013", "names": ["LM", "Lymphangioma", "lymphangioma", "LYMPHANGIOMA", "Lymphangiomas", "lymphangiomas", "Lymphangioma NOS", "Lymphangioma, NOS", "Benign lymphangioma", "benign lymphangioma", "lymphangioma, benign", "LYMPHANGIOMA, BENIGN", "Lymphangioendothelioma", "Lymphangioma, any site", "Capillary lymphangioma", "Lymphangioma (disorder)", "congenital lymphangioma", "Congenital lymphangioma", "Lymphangioma morphology", "benign lymphangioma (diagnosis)", "Lymphangioma of unspecified site", "Congenital lymphangioma (disorder)", "Benign lymphangioma (morphologic abnormality)", "benign lymphangioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphangioma", "shortest_name_length": 2}
{"curie": "UMLS:C4520761", "names": ["Stage I Sinonasal Squamous Cell Carcinoma AJCC v6 and v7", "Stage I Nasal Cavity and Paranasal Sinus Squamous Cell Cancer", "Stage I Nasal Cavity and Paranasal Sinus Squamous Cell Carcinoma", "Stage I Nasal Cavity and Paranasal Sinus Squamous Cell Carcinoma AJCC v7", "Stage I Nasal Cavity and Paranasal Sinus Squamous Cell Carcinoma AJCC v6", "Stage I Nasal Cavity and Paranasal Sinus Squamous Cell Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Sinonasal Squamous Cell Carcinoma AJCC v6 and v7", "shortest_name_length": 56}
{"curie": "UMLS:C2981399", "names": ["Stage IIB Colorectal Cancer", "Stage IIB Colorectal Cancer AJCC v7", "Stage IIB Colorectal (Colon or Rectal) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Colorectal Cancer AJCC v7", "shortest_name_length": 27}
{"curie": "MONDO:0013521", "names": ["DKCB4", "DKCA2", "autosomal dominant dyskeratosis congenita 2", "Dyskeratosis Congenita, Autosomal Dominant 2", "DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 2", "dyskeratosis congenita, autosomal dominant 2", "Dyskeratosis Congenita, Autosomal Recessive 4", "DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 4", "dyskeratosis congenita, autosomal recessive 4", "dyskeratosis congenita, autosomal dominant type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyskeratosis congenita, autosomal dominant 2", "shortest_name_length": 5}
{"curie": "MONDO:0031386", "names": ["cardioacrofacial dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardioacrofacial dysplasia", "shortest_name_length": 26}
{"curie": "UMLS:C5235863", "names": ["Neuroendocrine Carcinoma of Unknown Primary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neuroendocrine Carcinoma of Unknown Primary", "shortest_name_length": 43}
{"curie": "UMLS:C1882929", "names": ["Renal Diffuse Large B-Cell Lymphoma", "Kidney Diffuse Large B-Cell Lymphoma", "large B-cell diffuse lymphoma of kidney", "Diffuse Large B-Cell Lymphoma of the Kidney", "Primary Kidney Diffuse Large B-Cell Lymphoma", "large B-cell diffuse lymphoma of kidney (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "large B-cell diffuse lymphoma of kidney", "shortest_name_length": 35}
{"curie": "UMLS:C5667142", "names": ["Primary Meningeal Melanocytic Neoplasm", "Adult Primary Meningeal Melanocytic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Primary Meningeal Melanocytic Neoplasm", "shortest_name_length": 38}
{"curie": "UMLS:C0340530", "names": ["heart rejection transplant", "rejection heart transplant", "Heart transplant rejection", "heart transplant rejection", "heart rejection transplants", "Cardiac transplant rejection", "rejection; transplant, heart", "heart transplant rejection (diagnosis)", "Cardiac transplant rejection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiac transplant rejection", "shortest_name_length": 26}
{"curie": "UMLS:C1883338", "names": ["FTC, Minimally Invasive", "Follicular carcinoma, minimally invasive", "Thyroid Gland Follicular Carcinoma, Minimally Invasive", "minimally invasive follicular carcinoma of thyroid gland", "minimally invasive follicular carcinoma of the thyroid gland", "minimally invasive follicular carcinoma of the thyroid gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "minimally invasive follicular carcinoma of the thyroid gland", "shortest_name_length": 23}
{"curie": "MONDO:0008009", "names": ["MNLIX", "MONILETHRIX", "Nodose Hair", "Monilethrix", "hair beaded", "Beaded hair", "monilethrix", "beaded hair", "nodose hair", "Nodose Hairs", "Hair, Nodose", "beading hair", "Monilethrices", "Hairs, Nodose", "hair shaft beaded", "Congenital beaded hair", "congenital beaded hair", "Beaded hair (disorder)", "Congenital monilethrix", "Moniliform hair syndrome", "moniliform hair syndrome", "Beaded hair (physical finding)", "congenital beaded hair (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "monilethrix", "shortest_name_length": 5}
{"curie": "UMLS:C0877195", "names": ["Feminization acquired", "Feminisation acquired", "Acquired Feminization", "acquired feminization", "acquired feminization (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired Feminization", "shortest_name_length": 21}
{"curie": "MONDO:0009060", "names": ["Multiple lung cysts", "Cystic lung disease", "lung disease; cystic", "cystic; lung disease", "Cystic disease of lung", "cystic disease of lung", "CYSTIC DISEASE OF LUNG", "Multiple cysts of lung", "Cystic Disease Of Lung", "Multiple pulmonary cysts", "Multiple cysts of lung (disorder)", "disease (or disorder); cystic, lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cystic disease of lung", "shortest_name_length": 19}
{"curie": "UMLS:C5204270", "names": ["Renal Solitary Fibrous Tumor", "Kidney Solitary Fibrous Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kidney Solitary Fibrous Tumor", "shortest_name_length": 28}
{"curie": "MONDO:0001749", "names": ["Cortical senile cataract", "cortical cataract senile", "cortical senile cataract", "lens cortex senile cataract", "senile cataract of lens cortex", "Cortical senile cataract (disorder)", "cortical cataract senile (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cortical senile cataract", "shortest_name_length": 24}
{"curie": "UMLS:C5556700", "names": ["Advanced Mucosal Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Mucosal Melanoma", "shortest_name_length": 25}
{"curie": "MONDO:0006559", "names": ["Acne inversa", "acne inversa", "Acne Inversa", "ectopic acne", "apocrine acne", "Acne Inversas", "Inversa, Acne", "Apocrine acne", "Smoker's boils", "Inversas, Acne", "fox den disease", "verneuil disease", "verneuil's disease", "Verneuil's disease", "axillary hidradenitis", "acne inversa, familial", "Hidradenitis axillaris", "Acne inversa, familial", "axillaries hidradenitis", "Suppurative Hidradenitis", "Hidradenitis suppurativa", "Suppurative hidradenitis", "HIDRADENITIS SUPPURATIVA", "Hidradenitis Suppurativa", "hidradenitis suppurative", "suppurativa hidradenitis", "suppurative hidradenitis", "hidradenitis suppurativa", "HIDRADENITIS, SUPPURATIVA", "Hidradenitis, Suppurative", "Suppurative Hidradenitides", "Hidradenitides, Suppurative", "pyoderma fistulans significa", "Pyoderma fistulans significa", "Hidradenitis suppurativa (disorder)", "hidradenitis suppurativa (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hidradenitis suppurativa", "shortest_name_length": 12}
{"curie": "MONDO:0014933", "names": ["DEE44", "EIEE44", "early infantile epileptic encephalopathy 44", "developmental and epileptic encephalopathy 44", "epileptic encephalopathy, early infantile, 44", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 44", "UBA5 early infantile epileptic encephalopathy", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 44", "developmental and epileptic encephalopathy, 44", "epileptic encephalopathy, early infantile, type 44", "epileptic encephalopathy, early infantile, 44; EIEE44", "early infantile epileptic encephalopathy caused by mutation in UBA5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 44", "shortest_name_length": 5}
{"curie": "MONDO:0100074", "names": ["norovirus infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "norovirus infectious disease", "shortest_name_length": 28}
{"curie": "MONDO:0018201", "names": ["Extragonadal GCT, NOS", "EXTRAGONADAL GERM CELL TUMOR", "Extragonadal germ cell tumor", "extragonadal germ cell tumor", "Extragonadal Germ Cell Tumor", "germ cell tumor, extragonadal", "cell extragonadal germ tumors", "extragonadal germ cell neoplasm", "Extragonadal Germ Cell Neoplasm", "Tumor of Extragonadal Germ Cell", "tumor of extragonadal germ cell", "extragonadal germ cell neoplasms", "Extragonadal Germ Cell Neoplasms", "Neoplasm of Extragonadal Germ Cell", "Extragonadal germ cell tumors, NOS", "neoplasm of extragonadal germ cell", "tumor of the extragonadal germ cell", "Tumor of the Extragonadal Germ Cell", "primary extragonadal germ cell tumor", "Primary Extragonadal Germ Cell Tumor", "neoplasm of the extragonadal germ cell", "Neoplasm of the Extragonadal Germ Cell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extragonadal germ cell tumor", "shortest_name_length": 21}
{"curie": "MONDO:0018453", "names": ["FAMM Syndrome", "FAMM syndrome", "FAMMM syndrome", "FAMM-PC syndrome", "B-K mole syndrome", "familial Clark nevus syndrome", "familial atypical mole syndrome", "familial dysplastic nevus syndrome", "melanoma-pancreatic cancer syndrome", "Familial Atypical Mole Melanoma Syndrome", "familial atypical mole melanoma syndrome", "Familial atypical multiple mole melanoma (FAMMM)", "familial atypical multiple mole melanoma syndrome", "familial atypical multiple mole melanoma-pancreatic carcinoma syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial atypical multiple mole melanoma syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0003985", "names": ["chest wall cancer", "Chest Wall Lymphoma", "chest wall lymphoma", "lymphoma of chest wall", "Lymphoma of Chest Wall", "Lymphoma of the Chest Wall", "lymphoma of the chest wall", "Primary Chest Wall Lymphoma", "primary chest wall lymphoma", "malignant tumor of Chest Wall", "malignant neoplasm of chest wall"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chest wall lymphoma", "shortest_name_length": 17}
{"curie": "UMLS:C1699209", "names": ["intraoperative musculoskeletal injury", "Intraoperative musculoskeletal injury", "Intraoperative Musculoskeletal Injury", "intraoperative musculoskeletal injury (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraoperative Musculoskeletal Injury", "shortest_name_length": 37}
{"curie": "UMLS:C1868946", "names": ["Cerebral mass effect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebral mass effect", "shortest_name_length": 20}
{"curie": "MONDO:0010580", "names": ["DMSD", "XPID", "IPEX", "XLAAD", "IPEX syndrome", "Ipex Syndrome", "X linked Polyendocrinopathy", "X linked polyendocrinopathy", "autoimmune enteropathy type 1", "Autoimmune enteropathy type 1", "IDDM-secretory diarrhea syndrome", "IDDM-SECRETORY DIARRHEA SYNDROME", "islets of Langerhans, absence of", "ISLETS OF LANGERHANS, ABSENCE OF", "IDDM secretory diarrhea syndrome", "IDDM-Secretory Diarrhea Syndrome", "Iddm-secretory diarrhea syndrome", "immune dysfunction and diarrhea syndrome", "Immune Dysfunction and Diarrhea Syndrome", "autoimmunity-immunodeficiency syndrome X-linked", "autoimmunity-immunodeficiency syndrome, X-linked", "AUTOIMMUNITY-IMMUNODEFICIENCY SYNDROME, X-LINKED", "Autoimmunity-Immunodeficiency Syndrome, X-Linked", "X-linked autoimmunity-allergic dysregulation syndrome", "X-Linked Autoimmunity-Allergic Dysregulation Syndrome", "X-LINKED AUTOIMMUNITY-ALLERGIC DYSREGULATION SYNDROME", "diabetes mellitus type 1 with secretory diarrhea syndrome", "polyendocrinopathy, immune dysfunction and diarrhea X-linked", "POLYENDOCRINOPATHY, IMMUNE DYSFUNCTION, AND DIARRHEA, X-LINKED", "polyendocrinopathy, immune dysfunction, and diarrhea, X-linked", "Polyendocrinopathy, Immune Dysfunction, and Diarrhea, X-Linked", "immunodeficiency, polyendocrinopathy, and enteropathy, X-linked", "Insulin-dependent diabetes mellitus secretory diarrhea syndrome", "Immunodysregulation, polyendocrinopathy and enteropathy X-linked", "Insulin-dependent diabetes mellitus secretory diarrhoea syndrome", "diarrhea, polyendocrinopathy, fatal infection syndrome, X-linked", "DIARRHEA, POLYENDOCRINOPATHY, FATAL INFECTION SYNDROME, X-LINKED", "Diarrhea, Polyendocrinopathy, Fatal Infection Syndrome, X-Linked", "IMMUNODYSREGULATION, polyendocrinopathy, and enteropathy, X-linked", "IMMUNODYSREGULATION, POLYENDOCRINOPATHY, AND ENTEROPATHY, X-LINKED", "Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked", "immunodysregulation, polyendocrinopathy, and enteropathy, X-Linked", "immunodysregulation, polyendocrinopathy, and enteropathy, X-linked", "Immunodysregulation polyendocrinopathy enteropathy X-linked syndrome", "immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome", "Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome", "Enteropathy, Autoimmune, with Hemolytic Anemia and Polyendocrinopathy", "enteropathy, autoimmune, with hemolytic Anemia and polyendocrinopathy", "diabetes mellitus type 1 with secretory diarrhea syndrome (diagnosis)", "ENTEROPATHY, AUTOIMMUNE, WITH HEMOLYTIC ANEMIA AND POLYENDOCRINOPATHY", "IDDM - Insulin-dependent diabetes mellitus secretory diarrhea syndrome", "IDDM - Insulin-dependent diabetes mellitus secretory diarrhoea syndrome", "X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome", "Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome", "IMMUNODEFICIENCY, POLYENDOCRINOPATHY, AND ENTEROPATHY, X-LINKED, FORMERLY", "immunodeficiency, polyendocrinopathy, and enteropathy, X-linked, formerly", "Immune Dysregulation, Polyendocrinopathy, and Enteropathy X-linked Syndrome", "Immune Dysregulation, Polyendocrinopathy, and Enteropathy X-Linked Syndrome", "immune dysregulation, polyendocrinopathy, and enteropathy X-linked syndrome", "Congenital insulin-dependent diabetes mellitus with fatal secretory diarrhea", "Congenital insulin-dependent diabetes mellitus with fatal secretory diarrhoea", "diabetes mellitus, congenital insulin-dependent, with fatal secretory diarrhea", "Diabetes Mellitus, Congenital Insulin-Dependent, with Fatal Secretory Diarrhea", "DIABETES MELLITUS, CONGENITAL INSULIN-DEPENDENT, WITH FATAL SECRETORY DIARRHEA", "X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome (disorder)", "immunodysregulation, polyendocrinopathy, and enteropathy, X-linked, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0854816", "names": ["Stage III Lymphoplasmacytic Lymphoma", "Ann Arbor Stage III Lymphoplasmacytic Lymphoma", "Lymphoplasmacytoid Lymphoma/Immunocytoma Stage III", "Lymphoplasmacytoid lymphoma/immunocytoma stage III", "Stage III Lymphoplasmacytoid Lymphoma/Immunocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoplasmacytoid lymphoma/immunocytoma stage III", "shortest_name_length": 36}
{"curie": "MONDO:0100265", "names": ["peroxisome biogenesis disorder due to PEX5 defect in the PEX7-binding domain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder due to PEX5 defect in the PEX7-binding domain", "shortest_name_length": 76}
{"curie": "UMLS:C4521725", "names": ["Stage II Esophageal Squamous Cell Cancer", "Clinical Stage II Esophageal Squamous Cell Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage II Esophageal Squamous Cell Carcinoma AJCC v8", "shortest_name_length": 40}
{"curie": "MONDO:0019813", "names": ["Congenital tricuspid stenosis", "congenital tricuspid stenosis", "TS - Congenital tricuspid stenosis", "Congenital tricuspid valve stenosis", "congenital tricuspid valve stenosis", "tricuspid valve stenosis congenital", "Congenital stenosis of tricuspid valve", "tricuspid (valve); stenosis, congenital", "stenosis; tricuspid (valve), congenital", "congenital tricuspid valve stenosis (diagnosis)", "Congenital stenosis of tricuspid valve (disorder)", "deformity; tricuspid (valve), congenital, stenosis", "tricuspid (valve); deformity, congenital, stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital tricuspid stenosis", "shortest_name_length": 29}
{"curie": "UMLS:C2363722", "names": ["Steroid psychosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Steroid psychosis", "shortest_name_length": 17}
{"curie": "UMLS:C0001882", "names": ["Airsickness", "airsickness", "AIR SICKNESS", "Air Sickness", "Air sickness", "air sickness", "Sickness, Air", "Air sickness (finding)", "airsickness (diagnosis)", "air; disease (travel sickness)", "disease (or disorder); airsickness (travel sickness)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Airsickness", "shortest_name_length": 11}
{"curie": "UMLS:C2678248", "names": ["Mood instability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mood instability", "shortest_name_length": 16}
{"curie": "MONDO:0027655", "names": ["allopurinol toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "allopurinol toxicity", "shortest_name_length": 20}
{"curie": "UMLS:C5238239", "names": ["Locally Advanced Bladder Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Bladder Carcinoma", "shortest_name_length": 34}
{"curie": "UMLS:C0730504", "names": ["Pseudostrabismus", "Pseudostrabismus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pseudostrabismus", "shortest_name_length": 16}
{"curie": "MONDO:0005055", "names": ["ks", "KS", "KSHV", "HHV8", "HHV 8", "Kaposi Sarcoma", "kaposi sarcoma", "KAPOSI SARCOMA", "Kaposi sarcoma", "Sarcoma;Kaposis", "Kaposis sarcoma", "KAPOSIS SARCOMA", "sarcoma; Kaposi", "Kaposis Sarcoma", "Kaposi; sarcoma", "Sarcoma, Kaposi", "kaposi's sarcoma", "Kaposi's sarcoma", "Kaposi's Sarcoma", "ENDOTHELIOSARCOMA", "Kaposi's sarcomas", "Sarcoma, Kaposi's", "sarcoma, Kaposi's", "CNS Kaposi Sarcoma", "Anal Kaposi Sarcoma", "Lung Kaposi Sarcoma", "human herpesvirus 8", "kaposi oral sarcoma", "Skin Kaposi Sarcoma", "ORAL KAPOSI SARCOMA", "[M]Kaposi's sarcoma", "Heart Kaposi Sarcoma", "Kaposi's sarcoma NOS", "anal Kaposi's sarcoma", "kaposi's lung sarcoma", "Kaposi; sarcoma, skin", "sarcoma; Kaposi, skin", "Penile Kaposi Sarcoma", "KS - Kaposi's sarcoma", "Skin Kaposi's Sarcoma", "Lung Kaposi's Sarcoma", "oral kaposi's sarcoma", "Kaposi Sarcoma of CNS", "Anal Kaposi's Sarcoma", "Palate Kaposi Sarcoma", "Kaposi's sarcoma, lung", "Kaposi's sarcoma, skin", "Gastric Kaposi Sarcoma", "KAPOSI CANCER, SARCOMA", "Corneal Kaposi Sarcoma", "Kaposi sarcoma of skin", "kaposi's sarcoma, oral", "penis Kaposi's sarcoma", "Heart Kaposi's Sarcoma", "Cardiac Kaposi Sarcoma", "AIDS, Kaposi's Sarcoma", "Kaposi sarcoma of lung", "kaposi's lungs sarcoma", "Kaposi; sarcoma, palate", "sarcoma; Kaposi, palate", "Palate Kaposi's Sarcoma", "Prostate Kaposi Sarcoma", "Penile Kaposi's Sarcoma", "palate Kaposi's sarcoma", "PULMONARY KAPOSI SARCOMA", "Kaposi's sarcoma, palate", "corneal Kaposi's sarcoma", "Kaposi's Sarcoma of Skin", "gastric Kaposi's sarcoma", "Kaposi sarcoma of cornea", "Kaposi's sarcoma of anus", "Cutaneous Kaposi Sarcoma", "Gastric Kaposi's Sarcoma", "Cardiac Kaposi's Sarcoma", "Kaposi's Sarcoma of Lung", "Kaposi's sarcoma of lung", "palate; Kaposi's sarcoma", "cardiac Kaposi's sarcoma", "Corneal Kaposi's Sarcoma", "Kaposi's Sarcoma of Anus", "KAPOSI SARCOMA CUTANEOUS", "cutaneous kaposi sarcoma", "Kaposi's sarcoma of skin", "Kaposi sarcoma of palate", "Kaposi's sarcoma of heart", "epidemic Kaposi's sarcoma", "Kaposi's sarcoma of penis", "Kaposi's Sarcoma of Penis", "Epidemic Kaposi's Sarcoma", "Prostate Kaposi's Sarcoma", "Esophageal Kaposi Sarcoma", "Kaposi's Sarcoma of Heart", "Epidemic Kaposi's sarcoma", "prostate Kaposi's sarcoma", "Kaposi's sarcoma of Heart", "Kaposi Sarcoma of the CNS", "pulmonary kaposi's sarcoma", "Kaposi's sarcoma, epidemic", "Kaposi's sarcoma of palate", "cutaneous Kaposi's sarcoma", "Pulmonary Kaposi's Sarcoma", "Esophagus Kaposi's Sarcoma", "Kaposi sarcoma herpesvirus", "AIDS with Kaposi's sarcoma", "Kaposi's Sarcoma of Palate", "kaposi's sarcoma of palate", "Kaposi's Sarcoma of Cornea", "Kaposi's sarcoma (disease)", "Gallbladder Kaposi Sarcoma", "pulmonary Kaposi's sarcoma", "Cutaneous Kaposi's Sarcoma", "Kaposi's sarcoma of cornea", "lymph node Kaposi's sarcoma", "esophageal Kaposi's sarcoma", "intestinal Kaposi's sarcoma", "Kaposi's sarcoma (disorder)", "Skin cancer, Kaposi sarcoma", "kaposi's sarcoma, cutaneous", "conjunctival Kaposi sarcoma", "Kaposi's sarcoma (clinical)", "AIDS-related Kaposi sarcoma", "Kaposi's sarcoma of the CNS", "kaposi's sarcoma, pulmonary", "AIDS-Related Kaposi Sarcoma", "Esophageal Kaposi's Sarcoma", "Conjunctival Kaposi Sarcoma", "Kaposi's Sarcoma of Prostate", "multiple hemorrhagic sarcoma", "Kaposi's sarcoma (diagnosis)", "Gallbladder Kaposi's Sarcoma", "Kaposi's Sarcoma of the Lung", "Kaposi's Sarcoma of the Anus", "gallbladder Kaposi's sarcoma", "Multiple Hemorrhagic Sarcoma", "Kaposi's Sarcoma of the Skin", "HIV disease; sarcoma, Kaposi", "soft tissue Kaposi's sarcoma", "Mediterranean Kaposi sarcoma", "Multiple hemorrhagic sarcoma", "Kaposi's Sarcoma of Esophagus", "Kaposi sarcoma of soft tissue", "AIDS-Related Kaposi's Sarcoma", "Kaposi's Sarcoma of the Penis", "Kaposi sarcoma of lymph nodes", "conjunctival Kaposi's sarcoma", "Kaposi sarcoma of conjunctiva", "sarcoma, multiple hemorrhagic", "aids-related kaposi's sarcoma", "AIDS Related Kaposi's Sarcoma", "Kaposi's sarcoma, unspecified", "HIV disease; Kaposi's sarcoma", "AIDS-related Kaposi's sarcoma", "Kaposi's Sarcoma of the Heart", "Kaposi's sarcoma, soft tissue", "Multiple haemorrhagic sarcoma", "Kaposi's Sarcoma AIDS Related", "Conjunctival Kaposi's Sarcoma", "Kaposi's sarcoma AIDS related", "Kaposi's sarcoma of esophagus", "Kaposi's sarcoma, lymph nodes", "Kaposi's Sarcoma of the Palate", "Kaposi's Sarcoma Epidemic Type", "Kaposi's sarcoma, AIDS related", "Kaposi's sarcoma of lymph node", "Kaposi's sarcoma epidemic type", "Kaposi; sarcoma, lymph node(s)", "sarcoma; Kaposi, lymph node(s)", "Kaposi's Sarcoma of the Cornea", "Kaposi's Sarcoma of Gallbladder", "non AIDS related Kaposi sarcoma", "Kaposi's sarcoma of conjunctiva", "Kaposi's sarcoma of soft tissue", "sarcoma, Kaposi's, AIDS related", "Kaposi's sarcoma of lymph nodes", "Kaposi's sarcoma of gallbladder", "Lymphadenopathic Kaposi Sarcoma", "Kaposi's Sarcoma of Conjunctiva", "Cutaneous (Skin) Kaposi Sarcoma", "AIDS-associated Kaposi's sarcoma", "Kaposi's Sarcoma of the Prostate", "Kaposi's sarcoma of soft tissues", "Kaposi's sarcoma of the prostate", "Lymphadenopathic Kaposi's Sarcoma", "Kaposi's Sarcoma of the Esophagus", "lymphadenopathic Kaposi's sarcoma", "sarcoma; Kaposi, unspecified site", "Kaposi; sarcoma, unspecified site", "Kaposi's sarcoma, unspecified site", "Kaposi's sarcoma of skin (disorder)", "Kaposi's sarcoma of lung (disorder)", "Kaposi's Sarcoma of the Conjunctiva", "Kaposi's sarcoma of the gallbladder", "Kaposi's Sarcoma of the Gallbladder", "Kaposi's sarcoma of lung (diagnosis)", "Kaposi's sarcoma of skin (diagnosis)", "gastric Kaposi's sarcoma (diagnosis)", "Kaposi's sarcoma of unspecified site", "Kaposi's sarcoma of penis (diagnosis)", "Kaposi's sarcoma of cornea (disorder)", "Kaposi's sarcoma of palate (disorder)", "Kaposi's sarcoma associated with AIDS", "Central Nervous System Kaposi Sarcoma", "Kaposi's sarcoma of palate (diagnosis)", "Kaposi's sarcoma of cornea (diagnosis)", "Kaposi; sarcoma, lymph node (multiple)", "sarcoma; Kaposi, lymph node (multiple)", "central nervous system Kaposi's sarcoma", "Multiple idiopathic hemorrhagic sarcoma", "lymph node; Kaposi's sarcoma (multiple)", "Kaposi sarcoma (morphologic abnormality)", "Kaposi's sarcoma, gastrointestinal sites", "Multiple idiopathic haemorrhagic sarcoma", "Kaposi Sarcoma of Central Nervous System", "SARCOMA, MULTIPLE IDIOPATHIC HEMORRHAGIC", "HIV disease resulting in Kaposi's sarcoma", "African lymphadenopathic Kaposi's sarcoma", "Kaposi's sarcoma of esophagus (diagnosis)", "AIDS related multiple hemorrhagic sarcoma", "Kaposi's sarcoma of soft tissue (disorder)", "Kaposi's sarcoma of gastrointestinal sites", "Kaposi's sarcoma of lymph nodes (disorder)", "multiple hemorrhagic sarcoma, AIDS related", "Kaposi's sarcoma of central nervous system", "Kaposi's sarcoma of lymph node (diagnosis)", "Kaposi's sarcoma of conjunctiva (disorder)", "Kaposi's sarcoma of conjunctiva (diagnosis)", "Kaposi's sarcoma of soft tissue (diagnosis)", "sarcoma; Kaposi, resulting from HIV disease", "sarcoma, multiple hemorrhagic, AIDS related", "Kaposi's sarcoma of gallbladder (diagnosis)", "Kaposi; sarcoma, resulting from HIV disease", "Kaposi Sarcoma of the Central Nervous System", "Multiple Idiopathic Pigmented Hemangiosarcoma", "Kaposi's sarcoma-associated herpesvirus (KSHV)", "Kaposi's sarcoma associated with AIDS (diagnosis)", "Autoimmune Deficiency Syndrome-Related Kaposi Sarcoma", "Kaposi's sarcoma with acquired immunodeficiency syndrome", "acquired immune deficiency syndrome related Kaposi's sarcoma", "Kaposi sarcoma with AIDS (acquired immunodeficiency syndrome)", "Kaposi's sarcoma with AIDS (acquired immunodeficiency syndrome)", "Kaposi's sarcoma with acquired immunodeficiency syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kaposi's sarcoma", "shortest_name_length": 2}
{"curie": "MONDO:0007866", "names": ["BAPS", "Bart-Pumphrey syndrome", "Bart-Pumphrey Syndrome", "BART-PUMPHREY SYNDROME", "Bart Pumphrey syndrome", "Knuckle pads, leuconychia and deafness", "Knuckle pads, deafness and leukonychia syndrome", "Knuckle pads, leuconychia and sensorineural deafness", "knuckle pads, leuconychia and sensorineural deafness", "Knuckle Pads, Leukonychia, and Sensorineural Deafness", "knuckle pads, leukonychia, and sensorineural deafness", "KNUCKLE PADS, LEUKONYCHIA, AND SENSORINEURAL DEAFNESS", "Knuckle pads, leukonychia, deafness, and keratosis palmoplantaris", "knuckle pads-leukonychia-sensorineural deafness-palmoplantar keratoderma syndrome", "Knuckle pads-leukonychia-sensorineural deafness-palmoplantar keratoderma syndrome", "knuckle pads-leukonychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome", "Knuckle pads-leukonychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome", "Knuckle pads-leukonychia-sensorineural hearing loss-palmoplantar keratoderma syndrome", "Knuckle pads, leukonychia, sensorineural deafness, palmoplantar hyperkeratosis syndrome", "Knuckle pads-leukonychia-sensorineural hearing loss-palmoplantar hyperkeratosis syndrome", "Knuckle pads, leukonychia, sensorineural deafness, palmoplantar hyperkeratosis syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bart-Pumphrey syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C4528218", "names": ["Indolent T-cell lymphoproliferative disorder of gastrointestinal tract", "Indolent T-Cell Lymphoproliferative Disorder of the Gastrointestinal Tract", "Indolent T-cell lymphoproliferative disorder of gastrointestinal tract (disorder)", "Indolent T-cell lymphoproliferative disorder of gastrointestinal tract (diagnosis)", "Indolent T-cell lymphoproliferative disorder of gastrointestinal tract (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Indolent T-cell lymphoproliferative disorder of gastrointestinal tract", "shortest_name_length": 70}
{"curie": "MONDO:0023282", "names": ["granulomatous hypophysitis", "idiopathic granulomatous hypophysitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "granulomatous hypophysitis", "shortest_name_length": 26}
{"curie": "UMLS:C5557376", "names": ["Vulvar Solitary Fibrous Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Solitary Fibrous Tumor", "shortest_name_length": 29}
{"curie": "UMLS:C1306067", "names": ["Drug induced paranoia", "drug-induced paranoid state", "Drug-induced paranoid state", "Paranoid state, drug-induced", "Paranoid state caused by drug", "Paranoid state induced by drugs", "drug-induced paranoid state (diagnosis)", "Paranoid state caused by drug (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drug-induced paranoid state", "shortest_name_length": 21}
{"curie": "UMLS:C0392167", "names": ["DRUG EFFECT PROLONGED", "Drug action prolonged", "Drug effect prolonged", "Drug action prolonged (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drug action prolonged", "shortest_name_length": 21}
{"curie": "UMLS:C4520731", "names": ["stage II melanoma", "Stage II Melanoma", "Stage II Melanoma of Skin", "Stage II Cutaneous Melanoma", "Stage II Melanoma of the Skin", "Stage II Skin Melanoma AJCC v6", "Stage II Skin Melanoma AJCC v7", "Stage II Malignant Skin Melanoma", "Stage II Cutaneous (Skin) Melanoma", "Stage II Malignant Melanoma of Skin", "Stage II Malignant Cutaneous Melanoma", "Malignant Melanoma (of Skin), Stage II", "Stage II Malignant Melanoma of the Skin", "Stage II Cutaneous Melanoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Cutaneous Melanoma AJCC v6 and v7", "shortest_name_length": 17}
{"curie": "UMLS:C0334224", "names": ["Malignant tumor - uncertain whether primary or metastatic", "Malignant tumour - uncertain whether primary or metastatic", "Malignant Neoplasm, Uncertain Whether Primary or Metastatic", "Neoplasm, malignant, uncertain whether primary or metastatic", "Unclassified tumor, malignant, uncertain whether primary or metastatic", "Unclassified tumour, malignant, uncertain whether primary or metastatic", "Neoplasm, malignant, uncertain whether primary or metastatic (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplasm, malignant, uncertain whether primary or metastatic", "shortest_name_length": 57}
{"curie": "MONDO:0017947", "names": ["HCHWA, Italian type", "ABetaE22K amyloidosis", "ABeta amyloidosis, Italian type", "cerebral amyloid angiopathy, APP-related, Italian variant", "hereditary cerebral hemorrhage with amyloidosis, Italian type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ABeta amyloidosis, Italian type", "shortest_name_length": 19}
{"curie": "MONDO:0018818", "names": ["facial diplegia with paresthesias", "facial diplegia with paresthesias variant of GBS", "facial diplegia with paresthesias variant of Guillain-Barré syndrome", "facial diplegia with paresthesias variant of Guillain-BarrC) syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "facial diplegia with paresthesias", "shortest_name_length": 33}
{"curie": "UMLS:C1868812", "names": ["Leukemic infiltration extramedullary", "Leukaemic infiltration extramedullary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leukemic infiltration extramedullary", "shortest_name_length": 36}
{"curie": "UMLS:C5208247", "names": ["Immune-mediated encephalitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immune-mediated encephalitis", "shortest_name_length": 28}
{"curie": "MONDO:0100370", "names": ["Acute hepatitis B", "Acute Hepatitis B", "hepatitis b acute", "acute hepatitis b", "Hepatitis B Acute", "acute b hepatitis", "HEPATITIS B ACUTE", "acute hepatitis B", "Hepatitis B, acute", "HEPATITIS, ACUTE TYPE B", "acute hepatitis B infection", "Acute Hepatitis B Infection", "Acute type B viral hepatitis", "acute type B viral hepatitis", "acute viral hepatitis B infection", "acute hepatitis B virus infection", "Acute type B viral hepatitis (disorder)", "acute hepatitis B infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute hepatitis B virus infection", "shortest_name_length": 17}
{"curie": "MONDO:0006670", "names": ["Meningitis bacterial", "bacterial meningitis", "Meningitis;bacterial", "Bacterial Meningitis", "Bacterial meningitis", "MENINGITIS BACTERIAL", "Meningitis, bacterial", "meningitis; bacterial", "Meningitis, Bacterial", "meningitis, bacterial", "bacterial; meningitis", "MENINGITIS, BACTERIAL", "bacterial meningitides", "Bacterial Meningitides", "Meningitides, Bacterial", "Meningitis bacterial NOS", "Meningitis, bacterial NOS", "Bacterial meningitis, NOS", "BM - Bacterial meningitis", "Bacteria infectious meningitis", "Bacterial meningitis (disorder)", "bacterial meningitis (diagnosis)", "Bacterial meningitis, unspecified", "Bacteria caused infectious meningitis", "Meningitis due to unspecified bacterium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bacterial meningitis", "shortest_name_length": 20}
{"curie": "MONDO:0003945", "names": ["Bone Angioma", "bone hemangioma", "Osseous Angioma", "Angioma of Bone", "Bone Hemangioma", "Hemangioma of Bone", "Hemangioma of bone", "hemangioma of bone", "osseous hemangioma", "Osseous Hemangioma", "Angioma of the Bone", "Haemangioma of bone", "Hemangioma of the Bone", "Bone Epithelioid Angioma", "bone epithelioid angioma", "Epithelioid Angioma of Bone", "bone epithelioid hemangioma", "Bone Epithelioid Hemangioma", "Osseous Epithelioid Angioma", "epithelioid angioma of bone", "osseous epithelioid angioma", "Hemangioma of bone (disorder)", "Osseous Epithelioid Hemangioma", "Epithelioid Hemangioma of Bone", "osseous epithelioid hemangioma", "epithelioid hemangioma of bone", "hemangioma of bone (diagnosis)", "epithelioid angioma of the bone", "Epithelioid Angioma of the Bone", "Epithelioid Hemangioma of the Bone", "epithelioid hemangioma of the bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bone epithelioid hemangioma", "shortest_name_length": 12}
{"curie": "MONDO:0010191", "names": ["VWD3", "Type 3 VWD", "VWD type 3", "VWD, TYPE 3", "VWD, type 3", "von Willebrand disease 3", "von Willebrand's disease 3", "Von Willebrand disease type 3", "von Willebrand disease type 3", "VON WILLEBRAND disease, type 3", "VON WILLEBRAND DISEASE, TYPE 3", "von Willebrand Disease, Type 3", "Von Willebrand disease, type 3", "Type 3 Von Willebrand's Disease", "von Willebrand's disease type 3", "von Willebrand disease type III", "VON WILLEBRAND DISEASE, TYPE III", "Von Willebrand Disease, Severe Form", "Hereditary von Willebrand disease type 3", "von Willebrand disease type 3 (diagnosis)", "Hereditary von Willebrand disease type 3 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "von Willebrand disease 3", "shortest_name_length": 4}
{"curie": "UMLS:C0751000", "names": ["anterior cerebral artery aneurysm", "Anterior Cerebral Artery Aneurysm", "Anterior cerebral artery aneurysm", "Aneurysm, Anterior Cerebral Artery", "Aneurysm of anterior cerebral artery", "aneurysm of anterior cerebral artery", "Aneurysm of anterior cerebral artery (disorder)", "aneurysm of anterior cerebral artery (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aneurysm, Anterior Cerebral Artery", "shortest_name_length": 33}
{"curie": "UMLS:C2939186", "names": ["Mood Alteration", "mood alteration", "Mood alteration", "disturbance mood", "mood disturbance", "Mood disturbances", "Alteration in mood", "Mood alteration NOS", "Alterations in mood", "Disturbance in mood", "Mood alteration, NOS", "Disturbance in mood, NOS", "Disturbance in mood (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disturbance in mood", "shortest_name_length": 15}
{"curie": "MONDO:0003918", "names": ["Angiomatous Meningioma", "angiomatous meningioma", "Angiomatous meningioma", "Angiomatous Meningiomas", "angiomatous; meningioma", "meningioma; angiomatous", "Meningioma, Angiomatous", "Meningiomas, Angiomatous", "Angiomatous meningioma (morphologic abnormality)", "angiomatous meningioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angiomatous meningioma", "shortest_name_length": 22}
{"curie": "MONDO:0023646", "names": ["Lipodermatosclerosis", "lipodermatosclerosis", "sclerosing panniculitis", "Lipodermatosclerosis, NOS", "acute lipodermatosclerosis", "Acute lipodermatosclerosis", "Post-phlebitic liposclerosis", "hypodermitis sclerodermaformis", "Lipodermatosclerosis (disorder)", "lipodermatosclerosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lipodermatosclerosis", "shortest_name_length": 20}
{"curie": "UMLS:C0347011", "names": ["Metastasis to bladder", "Metastasis to Bladder", "Metastases to Bladder", "metastasis to bladder", "Metastases to bladder", "metastasis to the bladder", "Metastatic tumor to bladder", "Metastatic tumour to bladder", "Metastatic Tumor to the Bladder", "metastasis to bladder (diagnosis)", "Metastatic Neoplasm to the Bladder", "Cancer metastatic to urinary bladder", "Metastatic Tumor to the Urinary Bladder", "Secondary malignant neoplasm of bladder", "secondary malignant neoplasm of bladder", "Metastatic malignant neoplasm of bladder", "Metastatic malignant neoplasm to bladder", "Metastatic Neoplasm to the Urinary Bladder", "Metastatic Malignant Neoplasm in the Bladder", "Secondary malignant neoplasm of bladder, NOS", "Metastatic Malignant Neoplasm to the Bladder", "secondary malignant neoplasm urinary bladder", "Metastatic malignant neoplasm to bladder, NOS", "Metastatic malignant neoplasm to bladder (disorder)", "secondary malignant neoplasm of bladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Neoplasm to the Bladder", "shortest_name_length": 21}
{"curie": "MONDO:0011708", "names": ["DFNA36", "autosomal dominant deafness 36", "Deafness, Autosomal Dominant 36", "DEAFNESS, AUTOSOMAL DOMINANT 36", "deafness, autosomal dominant 36", "deafness, autosomal dominant type 36", "autosomal dominant nonsyndromic deafness 36", "TMC1 autosomal dominant nonsyndromic deafness", "autosomal dominant nonsyndromic hearing loss 36", "autosomal dominant nonsyndromic deafness type 36", "autosomal dominant nonsyndromic deafness caused by mutation in TMC1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 36", "shortest_name_length": 6}
{"curie": "UMLS:C0278687", "names": ["stage III ovary cancer", "ovary cancer, stage III", "ovarian cancer stage iii", "stage III ovarian cancer", "Stage III Ovarian Cancer", "Ovarian cancer stage III", "Ovarian Cancer Stage III", "ovarian cancer, stage III", "Stage III Ovarian Carcinoma", "stage III ovarian carcinoma", "ovarian carcinoma, stage III", "AJCC Stage III Ovarian Cancer", "FIGO Stage III Ovarian Cancer", "FIGO Stage III Cancer of Ovary", "Stage III Ovarian Cancer AJCC v6", "FIGO Stage III Ovarian Carcinoma", "Stage III Ovarian Cancer AJCC v7", "FIGO Stage III Carcinoma of Ovary", "FIGO Stage III Cancer of the Ovary", "stage III ovarian epithelial cancer", "Ovarian epithelial cancer stage III", "Stage III Ovarian Epithelial Cancer", "ovarian epithelial cancer, stage III", "FIGO Stage III Carcinoma of the Ovary", "Stage III Ovarian Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian cancer stage III", "shortest_name_length": 22}
{"curie": "MONDO:0002551", "names": ["c-P angle neurinoma", "C-P Angle Neurinoma", "C-P angle neurinoma", "Cerebellopontine Angle Neurinoma", "cerebellopontine angle neurinoma", "Cerebellopontine Angle Schwannoma", "cerebellopontine angle schwannoma", "cerebellar Pontine angle neurinoma", "Cerebellar Pontine Angle Neurinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "c-P angle neurinoma", "shortest_name_length": 19}
{"curie": "UMLS:C4525656", "names": ["Stage I Jejunal Neuroendocrine Tumor", "Stage I Jejunal Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Jejunal Neuroendocrine Tumor AJCC v8", "shortest_name_length": 36}
{"curie": "MONDO:0013092", "names": ["GLM2", "PTEN malignant glioma", "glioma susceptibility 2", "GLIOMA SUSCEPTIBILITY 2", "glioma susceptibility type 2", "malignant glioma caused by mutation in PTEN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glioma susceptibility 2", "shortest_name_length": 4}
{"curie": "MONDO:0001996", "names": ["Steroid responder - borderline", "Steroid-induced glaucoma - borderline", "borderline glaucoma steroid responder", "Borderline glaucoma steroid responder", "steroid-induced glaucoma - borderline", "Steroid responders borderline glaucoma", "steroid responders borderline glaucoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "steroid-induced glaucoma - borderline", "shortest_name_length": 30}
{"curie": "UMLS:C1141928", "names": ["Anastomotic complication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anastomotic complication", "shortest_name_length": 24}
{"curie": "UMLS:C1262060", "names": ["Post procedural fistula"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post procedural fistula", "shortest_name_length": 23}
{"curie": "MONDO:0002621", "names": ["soft tissue osteosarcoma", "Soft Tissue Osteosarcoma", "extraosseous osteosarcoma", "Extraosseous Osteosarcoma", "Extraskeletal Osteosarcoma", "extraskeletal osteosarcoma", "Extraskeletal osteosarcoma", "Osteosarcoma extraskeletal", "Extraskeletal osteosarcomas", "Extraskeletal osteosarcoma NOS", "extraskeletal Osteogenic sarcoma", "extraskeletal osteogenic sarcoma", "Extraskeletal Osteogenic Sarcoma", "Extraskeletal osteosarcoma (disorder)", "OSTEOSARCOMA, EXTRASKELETAL, MALIGNANT", "osteosarcoma, extraskeletal, malignant", "Extraskeletal osteosarcoma (diagnosis)", "Extraskeletal osteosarcoma stage unspecified", "malignant neoplasm extraskeletal osteosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extraosseous osteosarcoma", "shortest_name_length": 24}
{"curie": "UMLS:C0038279", "names": ["Postpartum Sterility", "Sterility, Postpartum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sterility, Postpartum", "shortest_name_length": 20}
{"curie": "MONDO:0009360", "names": ["HYC1", "HYDROCEPHALY", "hydrocephaly", "Ventriculomeglia", "Ventriculomegaly", "VENTRICULOMEGALY", "ventriculomegaly", "Cerebral Ventriculomegaly", "Cerebral ventriculomegaly", "Ventriculomegaly, Cerebral", "Cerebral Ventriculomegalies", "Ventriculomegalies, Cerebral", "hydrocephalus, congenital, 1", "HYDROCEPHALUS, CONGENITAL, 1", "CCDC88C congenital hydrocephalus", "Cerebral ventriculomegaly (disorder)", "hydrocephalus, nonsyndromic, autosomal recessive 1", "HYDROCEPHALUS, NONSYNDROMIC, AUTOSOMAL RECESSIVE 1", "congenital hydrocephalus caused by mutation in CCDC88C", "hydrocephalus, nonsyndromic, autosomal recessive type 1", "HYDROCEPHALUS, NONSYNDROMIC, AUTOSOMAL RECESSIVE 1, FORMERLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hydrocephalus, nonsyndromic, autosomal recessive 1", "shortest_name_length": 4}
{"curie": "MONDO:0019528", "names": ["IgG4-related hepatopathy", "inflammatory pseudotumor of the liver"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory pseudotumor of the liver", "shortest_name_length": 24}
{"curie": "MONDO:0001940", "names": ["Pleuropneumonia", "pleuropneumonia", "Pleuropneumonias", "Pleurobronchopneumonia", "Pleuropneumonia (disorder)", "Pleurobronchopneumonia (disorder)", "Pleurobronchopneumonia (diagnosis)", "bronchopneumonia pleurobronchopneumonia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pleuropneumonia", "shortest_name_length": 15}
{"curie": "UMLS:C2828198", "names": ["Stage I Bone Cancer", "Stage I Bone Cancer AJCC v7", "Stage I Bone Cancer  AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Bone Cancer AJCC v7", "shortest_name_length": 19}
{"curie": "MONDO:0008948", "names": ["CTx", "CTX", "Cholestanolosis", "VON BOGAERT DISEASE", "Cerebral Cholesterinoses", "CEREBRAL CHOLESTERINOSIS", "Cerebral cholesterinosis", "cerebral cholesterinosis", "Cerebral Cholesterinosis", "Van Bogaert-Scherer-Epstein", "Cholestanol storage disease", "cholestanol storage disease", "Cerebrotendinous Xanthomatosis", "CEREBROTENDINOUS XANTHOMATOSIS", "Cerebrotendinous xanthomatosis", "Cerebrotendinous Xanthomatoses", "cerebrotendinous xanthomatosis", "Xanthomatosis, Cerebrotendinous", "Xanthomatoses, Cerebrotendinous", "Cerebrotendinous cholesterinosis", "sterol 27-hydroxylase deficiency", "Sterol 27-hydroxylase deficiency", "Van Bogaert-Scherer-Epstein disease", "Van Bogaert-Scherer-Epstein Disease", "Van Bogaert Scherer Epstein Disease", "CTX - Cerebrotendinous xanthomatosis", "Bogaert-Scherer-Epstein Disease, Van", "van Bogaert-Scherer-Epstein syndrome", "Disease, Van Bogaert-Scherer-Epstein", "Cholestanol storage disease (disorder)", "Cerebrotendinous xanthomatosis syndrome", "cerebrotendinous xanthomatosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebrotendinous xanthomatosis", "shortest_name_length": 3}
{"curie": "MONDO:0015705", "names": ["AR-CNM", "autosomal recessive centronuclear myopathy", "Autosomal recessive centronuclear myopathy", "Autosomal Recessive Centronuclear Myopathy", "centronuclear myopathy, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive centronuclear myopathy", "shortest_name_length": 6}
{"curie": "UMLS:C0334592", "names": ["Cerebellar sarcoma", "cerebellar sarcoma", "Cerebellar Sarcoma", "sarcoma; cerebellar", "cerebellar; sarcoma", "sarcoma of cerebellum", "Cerebellar sarcoma NOS", "Cerebellar sarcoma, NOS", "cerebellar sarcoma (diagnosis)", "sarcoma of cerebellum (diagnosis)", "Cerebellar sarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebellar sarcoma", "shortest_name_length": 18}
{"curie": "MONDO:0011979", "names": ["AVMD", "VMD3", "AOFMD", "Gass disease", "Pseudo-Best disease", "pseudo-Best disease", "adult onset vitelliform dystrophy", "MACULAR DYSTROPHY, VITELLIFORM, 3", "macular dystrophy, vitelliform, 3", "adult-onset foveomacular dystrophy", "Adult-Onset Foveomacular Dystrophy", "Adult-onset foveomacular dystrophy", "Dystrophy, Adult-Onset Foveomacular", "Foveomacular Dystrophy, Adult-Onset", "Foveomacular Dystrophy, Adult Onset", "FOVEOMACULAR DYSTROPHY, ADULT-ONSET", "Adult vitelliform macular dystrophy", "Pseudo-vitelliform macular dystrophy", "pseudo-vitelliform macular dystrophy", "Adult-Onset Foveomacular Dystrophies", "Dystrophies, Adult-Onset Foveomacular", "Foveomacular Dystrophies, Adult-Onset", "macular dystrophy, vitelliform, type 3", "Adult Onset Vitelliform Macular Dystrophy", "Adult-onset vitelliform macular dystrophy", "adult-onset vitelliform macular dystrophy", "Adult-Onset Vitelliform Macular Dystrophy", "Vitelliform Macular Dystrophy, Adult-Onset", "foveomacular dystrophy, adult-onset; AOFMD", "VITELLIFORM MACULAR DYSTROPHY, ADULT-ONSET", "Vitelliform Macular Dystrophy, Adult Onset", "macular dystrophy, vitelliform, adult-onset", "Macular Dystrophy, Vitelliform, Adult-Onset", "adult onset vitelliform dystrophy (diagnosis)", "Adult-onset foveomacular vitelliform dystrophy", "Adult vitelliform macular dystrophy (disorder)", "adult-onset foveomacular vitelliform dystrophy", "adult-onset foveomacular dystrophy with choroidal neovascularization", "Adult-onset foveomacular dystrophy with choroidal neovascularization", "Foveomacular Dystrophy, Adult-Onset, With Choroidal Neovascularization", "foveomacular dystrophy, adult-onset, with choroidal neovascularization", "FOVEOMACULAR DYSTROPHY, ADULT-ONSET, WITH OR WITHOUT CHOROIDAL NEOVASCULARIZATION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult-onset foveomacular vitelliform dystrophy", "shortest_name_length": 4}
{"curie": "UMLS:C0000772", "names": ["ANOMALY MULTIPLE", "anomaly; multiple", "multiple; anomaly", "Multiple anomalies", "anomalies multiple", "deformity; multiple", "multiple; deformity", "MALFORMATIONS MULTIPLE", "Multiple Abnormalities", "Malformations multiple", "Abnormalities, Multiple", "multiple congenital anomaly", "MULTIPLE CONGENITAL ANOMALIES", "Anomalies congenital multiple", "Multiple Congenital Anomalies", "multiple congenital anomalies", "Multiple congenital anomalies", "ANOMALIES CONGENITAL MULTIPLE", "Congenital anomaly nos/multiple", "Congenital anomaly, multiple NOS", "ANOMALY CONGENITAL MULTIPLE (NOS)", "Multiple congenital anomalies NOS", "Multiple congenital abnormalities", "Multiple congenital malformations", "abnormalities congenital multiple", "Anomaly congenital multiple (NOS)", "Multiple congenital anomalies, NOS", "Congenital deformity, multiple NOS", "Multiple congenital deformities NOS", "multiple congenital anomalies (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Multiple congenital anomalies", "shortest_name_length": 16}
{"curie": "UMLS:C1408443", "names": ["obstruction; vagina", "VAGINAL OBSTRUCTION", "vaginal obstruction", "Vaginal obstruction", "vagina; obstruction", "Vaginal Obstruction", "vaginal obstruction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal obstruction", "shortest_name_length": 19}
{"curie": "MONDO:0006282", "names": ["lymphangiosarcoma", "Lymphangiosarcoma", "Lymphangiosarcomas", "Lymphangiosarcoma NOS", "skin lymphangiosarcoma", "Stewart-Treves syndrome", "LYMPHANGIOSARCOMA, MALIGNANT", "lymphangiosarcoma, malignant", "Lymphangiosarcoma (disorder)", "lymphangioendothelial sarcoma", "lymphangiosarcoma (diagnosis)", "Lymphangioendothelial Sarcoma", "Lymphangioendothelial sarcoma", "lymphangioendothelial; sarcoma", "sarcoma; lymphangioendothelial", "malignant Lymphangioendothelioma", "Malignant Lymphangioendothelioma", "malignant lymphangioendothelioma", "Malignant lymphangioendothelioma", "Lymphangioendothelioma, malignant", "Malignant Lymphangioendotheliomas", "Lymphangioendothelioma, Malignant", "Lymphangioendotheliomas, Malignant", "Lymphangiosarcoma of Stewart and Treves", "lymphangiosarcoma of Stewart and Treves", "Lymphangiosarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphangiosarcoma", "shortest_name_length": 17}
{"curie": "MONDO:0044726", "names": ["BILAPES", "BIRK-LANDAU-PEREZ SYNDROME", "Birk-Landau-Perez syndrome", "Cerebrorenal syndrome, Perez type", "psychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "psychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome", "shortest_name_length": 7}
{"curie": "UMLS:C4304995", "names": ["Recurrent Squamous Cell Carcinoma", "Recurrent squamous cell carcinoma", "Squamous cell carcinoma, recurrent", "Recurrent squamous cell carcinoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent squamous cell carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0019384", "names": ["Cruchet", "Economo", "Von Economo-Cruchet", "VON ECONOMO DISEASE", "von Economo disease", "ECONOMO ENCEPHALITIS", "economo encephalitis", "encephalitis; Vienna", "Vienna; encephalitis", "Epidemic encephalitis", "Von Economo’s disease", "epidemic encephalitis", "Von Economo's disease", "von Economo's disease", "Epidemic Encephalitis", "Arbovirus encephalitis", "epidemic; encephalitis", "encephalitis; epidemic", "encephalitis lethargic", "ENCEPHALITIS, EPIDEMIC", "Arbovirus Encephalitis", "arbovirus encephalitis", "lethargic encephalitis", "arboviral encephalitis", "LETHARGIC ENCEPHALITIS", "Arboviral encephalitis", "Encephalitis, Epidemic", "Arboviral Encephalitis", "Encephalitis, Arbovirus", "Encephalitis, Arboviral", "ENCEPHALITIS LETHARGICA", "ECONOMO-CRUCHET DISEASE", "Encephalitis lethargica", "Encephalitis Lethargica", "encephalitis; arboviral", "Epidemic Encephalitides", "arbovirus; encephalitis", "encephalitis lethargica", "Von Economo encephalitis", "lethargica; encephalitis", "Arbovirus Encephalitides", "Arboviral Encephalitides", "Encephalitides, Epidemic", "encephalitis; lethargica", "Encephalitides, Arbovirus", "Encephalitides, Arboviral", "von Economo's encephalitis", "Arbovirus encephalitis, NOS", "arthropod-borne encephalitis", "Arthropod Borne Encephalitis", "Arthropod-Borne Encephalitis", "Encephalitis, Arthropod-Borne", "encephalitis; arthropod-borne", "Encephalitis, Arthropod Borne", "arthropod-borne; encephalitis", "Arthropod-Borne Encephalitides", "Encephalitides, Arthropod-Borne", "Epidemic encephalitis (disorder)", "Arbovirus encephalitis (disorder)", "Arthropod-borne viral encephalitis", "arthropod-borne viral encephalitis", "Encephalitis lethargica (disorder)", "Arthropod Borne Viral Encephalitis", "Arthropod-Borne Viral Encephalitis", "Viral Encephalitis, Arthropod Borne", "Viral Encephalitis, Arthropod-Borne", "Encephalitis, Arthropod-Borne Viral", "viral; encephalitis, arthropod-borne", "Arthropod-Borne Viral Encephalitides", "encephalitis; viral, arthropod-borne", "Encephalitides, Arthropod-Borne Viral", "Viral Encephalitides, Arthropod-Borne", "encephalitis due to arthropod-borne virus", "Arthropod-borne viral encephalitis, vector unknown", "encephalitis due to arthropod-borne virus (diagnosis)", "Arthropod-borne viral encephalitis, vector unknown (navigational concept)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephalitis lethargica", "shortest_name_length": 7}
{"curie": "MONDO:0012823", "names": ["CRCS7", "colorectal cancer, susceptibility to, 7", "COLORECTAL CANCER, SUSCEPTIBILITY TO, 7", "colorectal cancer, susceptibility to, on chromosome 11", "COLORECTAL CANCER, SUSCEPTIBILITY TO, ON CHROMOSOME 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorectal cancer, susceptibility to, 7", "shortest_name_length": 5}
{"curie": "UMLS:C1710027", "names": ["Ancient Thymoma", "Sclerosing Thymoma", "Sclerosing thymoma", "Sclerosing thymoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sclerosing thymoma", "shortest_name_length": 15}
{"curie": "UMLS:C0855097", "names": ["Refractory Small Lymphocytic Lymphoma", "Refractory B-Cell Small Lymphocytic Lymphoma", "B-Cell Small Lymphocytic Lymphoma Refractory", "B-cell small lymphocytic lymphoma refractory", "Small lymphocyte B lymphoma (Lukes-Collins Classification) refractory"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-cell small lymphocytic lymphoma refractory", "shortest_name_length": 37}
{"curie": "MONDO:0006634", "names": ["Acidophil Adenoma", "Acidophil adenoma", "acidophil adenoma", "Eosinophil adenoma", "Eosinophil Adenoma", "eosinophil adenoma", "Acidophil Adenomas", "Adenoma, Acidophil", "Adenomas, Acidophil", "Eosinophil Adenomas", "Adenoma, Eosinophil", "Acidophilic Adenoma", "Adenomas, Eosinophil", "Adenoma, Acidophilic", "Acidophilic Adenomas", "Eosinophilic Adenoma", "Adenomas, Acidophilic", "Eosinophilic Adenomas", "Adenoma, Eosinophilic", "Adenomas, Eosinophilic", "pituitary eosinophilic adenoma", "pituitary adenoma, eosinophilic", "eosinophilic adenoma, pituitary", "adenoma, eosinophilic, pituitary", "growth hormone secreting adenoma", "pituitary gland acidophil adenoma", "adenoma, growth hormone secreting", "Pituitary Gland Acidophil Adenoma", "Acidophil adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pituitary gland acidophil adenoma", "shortest_name_length": 17}
{"curie": "UMLS:C1334412", "names": ["ASIN-L", "Low Grade Anal Canal Dysplasia", "Low Grade Anal Canal Squamous Dysplasia", "Low Grade Anal Canal Intraepithelial Neoplasia", "Low-Grade Intraepithelial Neoplasia of Anal Canal", "Low Grade Anal Squamous Intraepithelial Neoplasia", "Low-Grade Intraepithelial Neoplasia of the Anal Canal", "Low Grade Anal Canal Squamous Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Grade Anal Canal Intraepithelial Neoplasia", "shortest_name_length": 6}
{"curie": "MONDO:0013844", "names": ["STUT4", "stuttering, familial persistent, 4", "STUTTERING, FAMILIAL PERSISTENT, 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stuttering, familial persistent, 4", "shortest_name_length": 5}
{"curie": "MONDO:0008721", "names": ["MCAD", "MCADD", "ACADMD", "MCAD Deficiency", "mcad deficiency", "MCAD deficiency", "MCAD DEFICIENCY", "ACADM deficiency", "ACADM DEFICIENCY", "MCADH DEFICIENCY", "ACADM Deficiency", "Mcadh deficiency", "MCADH Deficiency", "Medium-Chain Acyl-CoA Dehydrogenase Deficiency", "medium chain acyl-CoA dehydrogenase deficiency", "Medium chain acyl-CoA dehydrogenase deficiency", "medium-chain acyl-CoA dehydrogenase deficiency", "Medium Chain Acyl-Coa Dehydrogenase Deficiency", "Medium-chain acyl-CoA dehydrogenase deficiency", "Medium chain acyl CoA dehydrogenase deficiency", "Medium-chain Acyl-CoA dehydrogenase deficiency", "medium chain acyl CoA dehydrogenase deficiency", "acyl-CoA dehydrogenase, medium-chain deficiency", "Acyl-CoA Dehydrogenase, Medium-Chain Deficiency", "acyl-CoA dehydrogenase medium chain deficiency of", "Deficiency of medium-chain acyl-CoA dehydrogenase", "acyl-CoA dehydrogenase, medium-chain, deficiency OF", "ACYL-CoA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF", "Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of", "Acyl-CoA dehydrogenase, medium chain, deficiency of", "medium-chain acyl-Coenzyme A dehydrogenase deficiency", "MCAD - Medium chain acyl-CoA dehydrogenase deficiency", "Medium chain acyl CoA dehydrogenase deficiency (MCAD)", "Medium chain acyl-coenzyme A dehydrogenase deficiency", "medium chain acyl-coenzyme A dehydrogenase deficiency", "Medium-chain acyl-coenzyme A dehydrogenase deficiency", "Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency", "medium-chain acyl-CoA dehydrogenase deficiency (diagnosis)", "Medium-chain acyl-coenzyme A dehydrogenase deficiency (disorder)", "Carnitine deficiency secondary to medium-chain acyl-CoA dehydrogenase deficiency", "Carnitine deficiency secondary to medium-chain acyl-Coa dehydrogenase deficiency", "Carnitine Deficiency Secondary To Medium-Chain Acyl-Coa Dehydrogenase Deficiency", "CARNITINE DEFICIENCY SECONDARY TO MEDIUM-CHAIN ACYL-CoA DEHYDROGENASE DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "medium chain acyl-CoA dehydrogenase deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0003851", "names": ["homunculus", "Homunculus", "Ovarian Fetiform Teratoma", "ovarian fetiform teratoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian fetiform teratoma", "shortest_name_length": 10}
{"curie": "MONDO:0011248", "names": ["deletion 13q32", "Deletion 13q32", "Monosomy 13q32", "13q32 deletion", "monosomy 13q32", "Distal 13q deletion", "distal monosomy 13q", "Distal monosomy 13q", "distal 13q deletion", "Telomeric deletion13q", "telomeric deletion13q", "distal monosomy type 13q", "Distal monosomy 13q syndrome", "Distal monosomy 13q syndrome (disorder)", "Distal monosomy 13q syndrome (diagnosis)", "Anal Atresia, Hypospadias, and Penoscrotal Inversion", "anal atresia, hypospadias, and penoscrotal inversion", "ANAL ATRESIA, HYPOSPADIAS, AND PENOSCROTAL INVERSION", "deletion of part of chromosome 13 long arm distal monosomy 13q syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal monosomy 13q", "shortest_name_length": 14}
{"curie": "MONDO:0007481", "names": ["LWD", "DCO", "DCo", "Leri", "Leri-Weill", "dyschondrosteosis", "Dyschondrosteosis", "DYSCHONDROSTEOSIS", "Leri-Weil syndrome", "Madelung deformity", "Leri-Weill syndrome", "Léri-Weill syndrome", "Leri-Weill Syndrome", "leri-weill syndrome", "Leri-Weill dyschondrostosis", "Leri-Weill dyschondrosteosis", "leri-weill dyschondrosteosis", "Leri-weill dyschondrosteosis", "Léri-Weill dyschondrosteosis", "Leri-Weill Dyschondrosteosis", "Léri-Weill Dyschondrosteosis", "Leri Weill dyschondrosteosis", "LERI-WEILL DYSCHONDROSTEOSIS", "Leri-Weill dyschondrosteosis syndrome", "Leri-Weill dyschondrosteosis (disorder)", "Leri-Weill dyschondrosteosis, Pseudoautosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leri-Weill dyschondrosteosis", "shortest_name_length": 3}
{"curie": "MONDO:0007119", "names": ["isolated aniridia", "nonsyndromic aniridia", "aniridia without systemic involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated aniridia", "shortest_name_length": 17}
{"curie": "UMLS:C0342257", "names": ["complicate diabetes", "Diabetes;complicated", "complicated diabetes", "Diabetic Complication", "Diabetes Complication", "DIABETIC COMPLICATION", "complication diabetic", "Diabetic complication", "diabetic complication", "Diabetic complications", "Diabetes Complications", "Diabetic Complications", "diabetic complications", "complications diabetic", "complications diabetics", "Diabetes--Complications", "Diabetic complication NOS", "Diabetic complication, NOS", "Diabetes-Related Complication", "Diabetes Mellitus Complication", "Diabetes-Related Complications", "Diabetes Related Complications", "diabetes mellitus complication", "complication diabetes mellitus", "diabetes mellitus complications", "complications diabetes mellitus", "Diabetes Mellitus Complications", "Complications of Diabetes Mellitus", "Diabetes mellitus with complication", "diabetes mellitus with complication", "Diabetes mellitus with complications", "Complication due to diabetes mellitus", "Diabetes with unspecified complication", "Diabetes with unspecified complications", "Disorder associated with diabetes mellitus", "diabetes mellitus with complication (diagnosis)", "Complication due to diabetes mellitus (disorder)", "Unspecified diabetes mellitus with unspecified complication", "Unspecified diabetes mellitus with unspecified complications"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Complications of Diabetes Mellitus", "shortest_name_length": 19}
{"curie": "UMLS:C5556695", "names": ["Locally Advanced Cutaneous Squamous Cell Carcinoma of the Head and Neck"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Cutaneous Squamous Cell Carcinoma of the Head and Neck", "shortest_name_length": 71}
{"curie": "MONDO:0015395", "names": ["congenital subglottic stenosis", "Congenital subglottic stenosis", "Congenital Subglottic Stenoses", "Congenital Subglottic Stenosis", "Subglottic Stenosis, Congenital", "Subglottic Stenoses, Congenital", "Stenosis, Congenital Subglottic", "Stenoses, Congenital Subglottic", "congenital; subglottic stenosis", "congenital; stenosis, subglottic", "subglottic; stenosis, congenital", "stenosis; subglottic, congenital", "Congenital subglottic stenosis (disorder)", "congenital subglottic stenosis (diagnosis)", "congenital malformations of larynx subglottic stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital subglottic stenosis", "shortest_name_length": 30}
{"curie": "MONDO:0011224", "names": ["JMADUE", "HIRAYAMA DISEASE", "Hirayama disease", "Monomelic amyotrophy", "monomelic amyotrophy", "Amyotrophy, monomelic", "AMYOTROPHY, MONOMELIC", "amyotrophy, monomelic", "benign focal amyotrophy", "Benign focal amyotrophy", "Spinal muscular atrophy juvenile nonprogressive", "spinal muscular atrophy juvenile nonprogressive", "SPINAL MUSCULAR ATROPHY, JUVENILE, NONPROGRESSIVE", "spinal muscular atrophy, juvenile, nonprogressive", "Spinal Muscular Atrophy, Juvenile, Nonprogressive", "juvenile muscular atrophy of the distal upper limb", "Juvenile muscular atrophy of the distal upper limb", "juvenile muscular atrophy of distal upper extremity", "Juvenile muscular atrophy of distal upper extremity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "monomelic amyotrophy", "shortest_name_length": 6}
{"curie": "UMLS:C1275420", "names": ["Extraabdominal Desmoid", "Extra-abdominal desmoid", "Extraabdominal Fibromatosis", "Extraabdominal Desmoid Tumor", "Extra-abdominal fibromatosis", "Extra-abdominal desmoid tumor", "Extra-abdominal desmoid tumour", "Extra-abdominal fibromatosis (disorder)", "Extra-abdominal fibromatosis (diagnosis)", "neoplasm of uncertain behavior extra-abdominal fibromatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extra-abdominal fibromatosis", "shortest_name_length": 22}
{"curie": "UMLS:C1332476", "names": ["Bone Schwannoma", "Benign Bone Schwannoma", "Benign Bone Neurilemmoma", "Benign Schwannoma of Bone", "Benign Neurilemmoma of Bone", "Benign Schwannoma of the Bone", "Benign Neurilemmoma of the Bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone Schwannoma", "shortest_name_length": 15}
{"curie": "UMLS:C4520746", "names": ["stage III lip and oral cavity cancer", "Lip and Oral Cavity Cancer Stage III", "Stage III Lip and Oral Cavity Cancer", "lip and oral cavity cancer, stage III", "oral cavity and lip cancer, stage III", "Lip and Oral Cavity Carcinoma Stage III", "Stage III Lip and Oral Cavity Carcinoma", "Stage III Lip and Oral Cavity Cancer AJCC v6", "Stage III Lip and Oral Cavity Cancer AJCC v7", "Stage III Lip and Oral Cavity Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Lip and Oral Cavity Cancer AJCC v6 and v7", "shortest_name_length": 36}
{"curie": "MONDO:0006784", "names": ["disease hemorrhagic newborn", "Newborn Hemorrhagic Disease", "hemorrhagic disease newborn", "newborn hemorrhagic disease", "Newborn Hemorrhagic Diseases", "disease haemorrhagic newborn", "Neonatal vitamin K deficiency", "Vitamin K Deficiency Bleeding", "newborn; hemorrhagic disorder", "hemorrhagic disease of newborn", "vitamin K; deficiency, newborn", "Hemorrhagic disease of newborn", "deficiency; vitamin K, newborn", "Hemorrhagic Disease of Newborn", "Haemorrhagic disease of newborn", "Vitamin K deficiency of newborn", "Hemorrhagic diathesis of newborn", "Haemorrhagic diathesis of newborn", "Hemorrhagic disease of the newborn", "Vitamin K deficiency of the newborn", "Haemorrhagic disease of the newborn", "HDN - Hemorrhagic disease of newborn", "HDN - Haemorrhagic disease of newborn", "vitamin K deficiency bleeding in newborn", "Vitamin K Deficiency Bleeding in Newborn", "hemorrhagic disease of newborn (diagnosis)", "hemorrhagic disease of newborn due to vitamin K deficiency", "Hemorrhagic disease of the newborn due to vitamin K deficiency", "Haemorrhagic disease of the newborn due to vitamin K deficiency", "hemorrhagic disease of newborn due to vitamin K deficiency (diagnosis)", "Hemorrhagic disease of the newborn due to vitamin K deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemorrhagic disease of newborn", "shortest_name_length": 27}
{"curie": "MONDO:0021546", "names": ["spinal cord ependymal tumor", "Ependymal Tumor of Spinal Cord", "ependymal tumor of spinal cord"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ependymal tumor of spinal cord", "shortest_name_length": 27}
{"curie": "MONDO:0010408", "names": ["STAR", "STAR Syndrome", "STAR syndrome", "Star syndrome", "STAR SYNDROME", "STAR syndrome, X-linked dominant", "SYNDACTYLY WITH RENAL AND ANOGENITAL MALFORMATIONS", "Syndactyly with Renal and Anogenital Malformations", "syndactyly with renal and anogenital malformations", "syndactyly, telecanthus, anogenital and renal malformations", "toe syndactyly, telecanthus, anogenital and renal malformations", "Syndactyly-telecanthus-anogenital and renal malformations syndrome", "syndactyly-telecanthus-anogenital and renal malformations syndrome", "TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS", "toe syndactyly, telecanthus, and anogenital and renal malformations", "Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations", "Syndactyly, telecanthus, anogenital and renal malformation syndrome", "STAR (syndactyly, telecanthus, anogenital, renal malformation) syndrome", "Syndactyly, telecanthus, anogenital and renal malformation syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndactyly-telecanthus-anogenital and renal malformations syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0016478", "names": ["Beckwith-Wiedemann syndrome due to 11p15 translocation/inversion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Beckwith-Wiedemann syndrome due to 11p15 translocation/inversion", "shortest_name_length": 64}
{"curie": "MONDO:0015409", "names": ["Isolated congenital syngnathia", "isolated congenital syngnathia", "Isolated congenital syngnathia (disorder)", "isolated congenital maxillomandibular fusion", "Isolated congenital maxillomandibular fusion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated congenital syngnathia", "shortest_name_length": 30}
{"curie": "MONDO:0020483", "names": ["painful myotonia", "Painful myotonia", "ACZ-responsive myotonia", "Painful congenital myotonia", "painful congenital myotonia", "acetazolamide-responsive myotonia", "Acetazolamide-responsive myotonia", "Acetazolamide responsive myotonia", "ACZ-responsive congenital myotonia", "Myotonia-painful contractions syndrome", "myotonia-painful contractions syndrome", "Acetazolamide-responsive congenital myotonia", "Acetazolamide responsive myotonia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acetazolamide-responsive myotonia", "shortest_name_length": 16}
{"curie": "UMLS:C5392077", "names": ["ICUS", "Idiopathic Cytopenia of Undetermined Significance", "Idiopathic Cytopenias of Undetermined Significance", "ICUS Idiopathic Cytopenias of Undetermined Significance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Idiopathic Cytopenias of Undetermined Significance", "shortest_name_length": 4}
{"curie": "MONDO:0004430", "names": ["penis mixed squamous cell carcinoma", "mixed squamous cell carcinoma of the penis", "Mixed Squamous Cell Carcinoma of the Penis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "penis mixed squamous cell carcinoma", "shortest_name_length": 35}
{"curie": "MONDO:0017443", "names": ["radio-ulnar terminal transverse meromelia", "congenital absence of both forearm and hand"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital absence of both forearm and hand", "shortest_name_length": 41}
{"curie": "MONDO:0010455", "names": ["XMEN", "MAGT1 Deficiency", "Cid due to MAGT1 deficiency", "CID due to MAGT1 deficiency", "combined immunodeficiency due to MAGT1 deficiency", "Combined immunodeficiency due to MAGT1 deficiency", "X-linked magnesium deficiency with Epstein-Barr virus infection and neoplasia", "X-Linked Immunodeficiency with Magnesium Defect Epstein-Barr Virus Infection and Neoplasia", "X-Linked Immunodeficiency with Magnesium Defect, Epstein-Barr Virus Infection and Neoplasia", "X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia", "X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia", "IMMUNODEFICIENCY, X-LINKED, WITH MAGNESIUM DEFECT, EPSTEIN-BARR VIRUS INFECTION, AND NEOPLASIA", "immunodeficiency, X-linked, with magnesium defect, Epstein-Barr VIRUS infection, and neoplasia", "X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia (disorder)", "immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia", "shortest_name_length": 4}
{"curie": "UMLS:C0948031", "names": ["Primary Graft Dysfunction", "Primary graft dysfunction", "Graft Dysfunction, Primary", "Dysfunction, Primary Graft"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Graft Dysfunction", "shortest_name_length": 25}
{"curie": "MONDO:0019872", "names": ["Trisomy 3pter", "trisomy 3pter", "Distal trisomy 3p", "distal trisomy 3p", "Distal duplication 3p", "distal duplication 3p", "distal trisomy type 3p", "telomeric duplication 3p", "Telomeric duplication 3p", "Distal trisomy 3p (disorder)", "Distal trisomy 3p (diagnosis)", "anomaly of chromosome pair distal trisomy 3p"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal trisomy 3p", "shortest_name_length": 13}
{"curie": "UMLS:C4682431", "names": ["Vaginal Cancer by AJCC v8 Stage", "Vaginal Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Cancer by AJCC v8 Stage", "shortest_name_length": 31}
{"curie": "UMLS:C4682864", "names": ["Advanced Nonfunctional Neuroendocrine Tumor", "Advanced Non-Functioning Neuroendocrine Tumor", "Advanced Nonfunctional Well Differentiated Neuroendocrine Neoplasm", "Advanced Nonfunctioning Well Differentiated Neuroendocrine Neoplasm", "Advanced Non-Functioning Well Differentiated Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Non-Functioning Neuroendocrine Tumor", "shortest_name_length": 43}
{"curie": "MONDO:0010571", "names": ["FPO", "OPD2", "OPD 2 syndrome", "OPD Syndrome 2", "OPD SYNDROME 2", "OPD syndrome 2", "Andre syndrome", "OPD II SYNDROME", "OPD II Syndrome", "OPD II syndrome", "OPD Syndrome, Type 2", "Otopalatodigital syndrome", "Cranioorodigital Syndrome", "CRANIOORODIGITAL SYNDROME", "otopalatodigital syndrome", "cranioorodigital syndrome", "faciopalatoosseous syndrome", "Faciopalatoosseous syndrome", "FACIOPALATOOSSEOUS SYNDROME", "Cranio-oro-digital syndrome", "cranio-oro-digital syndrome", "otopalatodigital syndrome II", "facio-palato-osseous syndrome", "OPD - Otopalatodigital syndrome", "Otopalatodigital syndrome type 2", "otopalatodigital syndrome type 2", "otopalatodigital syndrome type II", "otopalatodigital syndrome, type 2", "OTOPALATODIGITAL SYNDROME, TYPE II", "oto-palato-digital syndrome type 2", "otopalatodigital (OPD) syndrome II", "otopalatodigital syndrome, type II", "Otopalatodigital Syndrome, Type II", "facio-palato-osseous (FPO) syndrome", "Oto-palato-digital syndrome, type 2", "Oto-palato-digital syndrome, type II", "otopalatodigital syndrome (diagnosis)", "Oto-palato-digital syndrome, type II (disorder)", "otopalatodigital syndrome, type II, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "otopalatodigital syndrome type 2", "shortest_name_length": 3}
{"curie": "MONDO:0030500", "names": ["LDS6", "Loeys-Dietz syndrome 6", "LOEYS-DIETZ SYNDROME 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Loeys-Dietz syndrome 6", "shortest_name_length": 4}
{"curie": "MONDO:0017616", "names": ["X-linked intellectual disability, Schutz type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability, Schutz type", "shortest_name_length": 45}
{"curie": "MONDO:0012530", "names": ["Palmoplantar Hyperkeratosis And True Hermaphroditism", "palmoplantar hyperkeratosis and true hermaphroditism", "PALMOPLANTAR HYPERKERATOSIS AND TRUE HERMAPHRODITISM", "palmoplantar hyperkeratosis with squamous cell carcinoma of skin and sex reversal", "palmoplantar hyperkeratosis with squamous cell carcinoma of skin and 46,XX SEX reversal", "PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL", "palmoplantar keratoderma-XX sex reversal-predisposition to squamous cell carcinoma syndrome", "palmoplantar hyperkeratosis-XX sex reversal-predisposition to squamous cell carcinoma syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "palmoplantar keratoderma-XX sex reversal-predisposition to squamous cell carcinoma syndrome", "shortest_name_length": 52}
{"curie": "UMLS:C2721735", "names": ["Infusion site discomfort"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infusion site discomfort", "shortest_name_length": 24}
{"curie": "UMLS:C0853971", "names": ["Inflammatory breast cancer stage III", "Stage IIIB Inflammatory Breast Cancer", "Stage IIIB Inflammatory Breast Carcinoma", "Stage IIIB Breast Inflammatory Carcinoma", "Stage IIIB Breast  Inflammatory Carcinoma", "Inflammatory carcinoma of breast stage III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Inflammatory carcinoma of breast stage III", "shortest_name_length": 36}
{"curie": "MONDO:0013568", "names": ["SSS3", "sick sinus syndrome 3", "MYH6 familial sick sinus syndrome", "susceptibility to sick sinus syndrome 3", "sick sinus syndrome 3, susceptibility to", "SICK SINUS SYNDROME 3, SUSCEPTIBILITY TO", "familial sick sinus syndrome caused by mutation in MYH6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sick sinus syndrome 3, susceptibility to", "shortest_name_length": 4}
{"curie": "MONDO:0000706", "names": ["chemical colitis", "Chemical colitis", "Toxic enterocolitis", "Chemically-induced colitis", "Chemical colitis (disorder)", "Other and unspecified noninfective gastroenteritis and colitis", "Other and unspecified noninfectious gastroenteritis and colitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chemical colitis", "shortest_name_length": 16}
{"curie": "MONDO:0017312", "names": ["Perrault syndrome", "XX-type gonadal dysgenesis", "Gonadal dysgenesis XX type deafness", "XX gonodal dysgenesis-deafness syndrome", "gonadal dysgenesis, XX type, with deafness", "GONADAL DYSGENESIS, XX TYPE, WITH DEAFNESS", "XX gonodal dysgenesis-hearing loss syndrome", "Ovarian dysgenesis with sensorineural deafness", "OVARIAN DYSGENESIS WITH SENSORINEURAL DEAFNESS", "ovarian dysgenesis-sensorineural deafness syndrome", "Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance", "Gonadal dysgenesis with sensorineural deafness, autosomal recessive inheritance", "Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perrault syndrome", "shortest_name_length": 17}
{"curie": "UMLS:C1708851", "names": ["Macrofollicular Variant Thyroid Gland Papillary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Macrofollicular Variant Thyroid Gland Papillary Carcinoma", "shortest_name_length": 57}
{"curie": "UMLS:C1336331", "names": ["Stage IVA Lip Basal Cell Cancer", "Stage IVA Basal Cell Lip Carcinoma", "Stage IVA Basal Cell Carcinoma of Lip", "Stage IVA Basal Cell Carcinoma of the Lip", "stage IVA basal cell carcinoma of the lip"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Basal Cell Lip Carcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C1720505", "names": ["Adult growth hormone deficiency", "Adult growth hormone deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult growth hormone deficiency", "shortest_name_length": 31}
{"curie": "UMLS:C1302773", "names": ["LSIL", "Low grade SIL", "Low Grade Squamous Intraepithelial Lesion", "Low grade squamous intraepithelial lesion", "Low-grade squamous intraepithelial lesion", "low-grade squamous intraepithelial lesion", "Low-Grade Squamous Intraepithelial Lesion", "Squamous intraepithelial neoplasia grade 1", "grade I squamous intraepithelial neoplasia", "Grade I Squamous Intraepithelial Neoplasia", "grade 1 squamous intraepithelial neoplasia", "Low Grade Squamous Intraepithelial Lesions", "Low-Grade Squamous Intraepithelial Lesions", "Grade 1 Squamous Intraepithelial Neoplasia", "Squamous intraepithelial neoplasia, grade I", "Low Grade Squamous Intraepithelial Neoplasia", "low-grade squamous intraepithelial neoplasia", "Squamous intraepithelial neoplasia, low grade", "LSIL, Low-Grade Squamous Intraepithelial Lesion", "LSIL, Low Grade Squamous Intraepithelial Lesion", "LSIL, Low Grade Squamous Intraepithelial Lesions", "LSIL, Low-Grade Squamous Intraepithelial Lesions", "Low-grade squamous intraepithelial lesion (morphologic abnormality)", "Squamous intraepithelial neoplasia grade 1 (morphologic abnormality)", "Squamous intraepithelial neoplasia, low grade (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Grade Squamous Intraepithelial Neoplasia", "shortest_name_length": 4}
{"curie": "MONDO:0008460", "names": ["SGFLD SYNDROME", "Sgfld syndrome", "SGFLD syndrome", "Splenogonadal Fusion Limb Defect Syndrome", "Splenogonadal fusion limb defect syndrome", "splenogonadal fusion limb defect syndrome", "SPLENOGONADAL FUSION LIMB DEFECT SYNDROME", "splenogonadal fusion limb defects syndrome", "Splenogonadal fusion limb defects syndrome", "Splenogonadal fusion limb defects micrognatia", "splenogonadal fusion limb defects micrognatia", "SPLENOGONADAL FUSION WITH LIMB DEFECTS AND MICROGNATHIA", "splenogonadal fusion with limb defects and micrognathia", "Splenogonadal Fusion with Limb Defects and Micrognathia", "splenogonadal fusion-limb defects-micrognathia syndrome", "Splenogonadal fusion-limb defects-micrognathia syndrome", "Splenogonadal fusion, limb defect, micrognathia syndrome", "SGFLD (splenogonadal fusion limb defect syndrome) syndrome", "Splenogonadal fusion, limb defect, micrognathia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "splenogonadal fusion-limb defects-micrognathia syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0023530", "names": ["kallikrein hypertension", "Kallikrein hypertension", "Kallikrein attenuated hypertension", "kallikrein attenuated hypertension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kallikrein hypertension", "shortest_name_length": 23}
{"curie": "UMLS:C4682571", "names": ["Stage III Uterine Corpus Endometrial Stromal Sarcoma", "Stage III Uterine Corpus Endometrial Stromal Sarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Uterine Corpus Endometrial Stromal Sarcoma AJCC v8", "shortest_name_length": 52}
{"curie": "MONDO:0010390", "names": ["OASD", "Ws2-Oa", "Deafness and ocular albinism", "DEAFNESS AND OCULAR ALBINISM", "deafness and ocular albinism", "Ocular albinism with sensorineural deafness", "ocular albinism with sensorineural deafness", "OCULAR ALBINISM WITH SENSORINEURAL DEAFNESS", "Albinism, Ocular, With Sensorineural Deafness", "albinism ocular late onset sensorineural deafness", "Albinism ocular late onset sensorineural deafness", "Ocular albinism with late-onset sensorineural deafness", "ocular albinism with late-onset sensorineural deafness", "albinism, ocular, with late-onset sensorineural deafness", "ALBINISM, OCULAR, WITH LATE-ONSET SENSORINEURAL DEAFNESS", "Albinism, Ocular, With Late-Onset Sensorineural Deafness", "Ocular albinism with late-onset sensorineural hearing loss", "Ocular albinism with late-onset sensorineural deafness (disorder)", "ALBINISM, OCULAR, WITH LATE-ONSET SENSORINEURAL DEAFNESS (disorder)", "Waardenburg Syndrome, Type Ii, With Ocular Albinism, Autosomal Recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ocular albinism with late-onset sensorineural deafness", "shortest_name_length": 4}
{"curie": "UMLS:C5669688", "names": ["Advanced Hilar Cholangiocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Hilar Cholangiocarcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C1336319", "names": ["Stage II Soft Tissue Sarcoma", "stage II soft tissue sarcoma", "Stage II Sarcoma of Soft Tissue", "Stage II Sarcoma of the Soft Tissue", "Stage II Soft Tissue Sarcoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Soft Tissue Sarcoma AJCC v7", "shortest_name_length": 28}
{"curie": "UMLS:C0744403", "names": ["Gum Infection", "gum infection", "Infection;gum", "Gum infection", "gum; infection", "gums infection", "gum infections", "infection; gum", "gums infections", "Infection of gum", "of gum infection", "infection gingiva", "infection; gingiva", "gingiva; infection", "gingival infection", "Gingival infection", "GINGIVAL INFECTION", "Gingival infections", "gingivitis infection", "Gingivitis infection", "Gingivitis infection NOS", "gingival infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gum Infection", "shortest_name_length": 13}
{"curie": "UMLS:C0278739", "names": ["Recurrent Lymphoblastic Lymphoma", "NHL, lymphoblastic recurrent childhood", "relapsed childhood lymphoblastic lymphoma", "Relapsed Pediatric Lymphoblastic Lymphoma", "relapsed lymphoblastic childhood lymphoma", "Relapsed Childhood Lymphoblastic Lymphoma", "Recurrent Pediatric Lymphoblastic Lymphoma", "recurrent lymphoblastic childhood lymphoma", "Recurrent Childhood Lymphoblastic Lymphoma", "recurrent childhood lymphoblastic lymphoma", "Recurrent Childhood Precursor Lymphoblastic Lymphoma", "lymphoblastic recurrent non-Hodgkin's lymphoma, childhood", "pediatric lymphoblastic non-Hodgkin's lymphoma, recurrent", "childhood non-Hodgkin's lymphoma, lymphoblastic recurrent", "non-Hodgkin's lymphoma, lymphoblastic recurrent, childhood", "lymphoma, non-Hodgkin's, lymphoblastic recurrent, childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Lymphoblastic Lymphoma", "shortest_name_length": 32}
{"curie": "UMLS:C4518349", "names": ["Intratubular Large Cell Hyalinizing Sertoli Cell Neoplasia", "Intratubular large cell hyalinising Sertoli cell neoplasia", "Intratubular large cell hyalinizing Sertoli cell neoplasia", "Intratubular large cell hyalinizing Sertoli cell neoplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intratubular large cell hyalinizing Sertoli cell neoplasia", "shortest_name_length": 58}
{"curie": "UMLS:C4524636", "names": ["IC", "Stage IC Esophageal Adenocarcinoma", "Pathologic Stage IC Esophageal Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IC Esophageal Adenocarcinoma AJCC v8", "shortest_name_length": 2}
{"curie": "UMLS:C1290379", "names": ["Acute cardiovascular disease", "acute cardiovascular disease", "cardiovascular disease acute", "Acute cardiovascular disorder", "Acute disease of cardiovascular system", "Acute disorder of cardiovascular system", "Acute disease of cardiovascular system (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute disease of cardiovascular system", "shortest_name_length": 28}
{"curie": "MONDO:0001637", "names": ["Cicatricial entropion", "cicatricial entropion", "Cicatricial entropion (disorder)", "cicatricial entropion (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cicatricial entropion", "shortest_name_length": 21}
{"curie": "UMLS:C5237039", "names": ["Recurrent Fallopian Tube High-Grade Serous Adenocarcinoma", "Recurrent High Grade Fallopian Tube Serous Adenocarcinoma", "Recurrent Fallopian Tube High Grade Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Fallopian Tube High Grade Serous Adenocarcinoma", "shortest_name_length": 57}
{"curie": "MONDO:0004144", "names": ["Fibrous meningioma", "Fibrous Meningioma", "fibrous meningioma", "Fibrous Meningiomas", "Meningioma, Fibrous", "fibrous; meningioma", "meningioma; fibrous", "Meningiomas, Fibrous", "fibroblastic meningioma", "Fibroblastic meningioma", "Fibroblastic Meningioma", "fibroblastic; meningioma", "meningioma; fibroblastic", "fibrous meningioma (morphologic abnormality)", "Fibrous meningioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibrous meningioma", "shortest_name_length": 18}
{"curie": "MONDO:0014392", "names": ["DEE25", "EIEE25", "SLC13A5 Deficiency", "SLC13A5 deficiency", "early infantile epileptic encephalopathy 25", "Early Infantile Epileptic Encephalopathy 25", "Developmental and Epileptic Encephalopathy 25", "developmental and epileptic encephalopathy 25", "epileptic encephalopathy, early infantile, 25", "developmental and epileptic encephalopathy, 25", "SLC13A5 early infantile epileptic encephalopathy", "epileptic encephalopathy, early infantile, type 25", "early infantile epileptic encephalopathy caused by mutation in SLC13A5", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 25 WITH AMELOGENESIS IMPERFECTA", "developmental and epileptic encephalopathy 25, with amelogenesis imperfecta", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 25, WITH AMELOGENESIS IMPERFECTA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 25", "shortest_name_length": 5}
{"curie": "UMLS:C0270496", "names": ["Schizoaffective disorder bipolar type", "Schizoaffective disorder, Bipolar type", "SCHIZO AFFECTIVE DISORDER BIPOLAR TYPE", "Schizoaffective disorder, bipolar type", "disorder; schizoaffective, bipolar type", "schizoaffective; disorder, bipolar type", "Schizoaffective disorder, bipolar type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Schizoaffective disorder, bipolar type", "shortest_name_length": 37}
{"curie": "MONDO:0004303", "names": ["Parathyroid Clear Cell Adenoma", "parathyroid clear cell adenoma", "clear cell adenoma of parathyroid", "Clear Cell Adenoma of Parathyroid", "Parathyroid Gland Clear Cell Adenoma", "parathyroid gland clear cell adenoma", "clear cell adenoma of the parathyroid", "Clear Cell Adenoma of the Parathyroid", "Clear cell adenoma of the Parathyroid", "clear celladenoma of parathyroid gland", "Clear Cell Adenoma of Parathyroid Gland", "clear cell adenoma of parathyroid gland", "clear cell adenoma of the parathyroid gland", "Parathyroid transitional clear cell adenoma", "Parathyroid Transitional Clear Cell Adenoma", "Clear Cell Adenoma of the Parathyroid Gland", "parathyroid transitional clear cell adenoma", "transitional clear cell adenoma of parathyroid", "Transitional Clear Cell Adenoma of Parathyroid", "parathyroid gland transitional clear cell adenoma", "Parathyroid Gland Transitional Clear Cell Adenoma", "Transitional Clear Cell Adenoma of the Parathyroid", "transitional clear cell adenoma of the parathyroid", "Transitional Clear Cell Adenoma of Parathyroid Gland", "transitional clear cell adenoma of parathyroid gland", "transitional clear cell adenoma of the parathyroid gland", "Transitional Clear Cell Adenoma of the Parathyroid Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parathyroid gland clear cell adenoma", "shortest_name_length": 30}
{"curie": "UMLS:C4726547", "names": ["Refractory Digestive System Carcinoma", "Refractory Gastrointestinal System Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Digestive System Carcinoma", "shortest_name_length": 37}
{"curie": "UMLS:C0919582", "names": ["Sudden onset of sleep"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sudden onset of sleep", "shortest_name_length": 21}
{"curie": "MONDO:0014238", "names": ["MRT39", "mental retardation, autosomal recessive 39", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 39", "mental retardation, autosomal recessive type 39", "intellectual disability, autosomal recessive 39", "intellectual disability, autosomal recessive type 39", "autosomal recessive intellectual developmental disorder 39", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 39", "severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0424187", "names": ["needle fear", "fear needles", "Trypanophobia", "injection fear", "fear of needles", "Phobia, needles", "Fear of needles", "Fear of injection", "Phobia, injections", "Fear of injections", "Fear of needles (finding)", "Fear of needles or injections"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fear of needles", "shortest_name_length": 11}
{"curie": "MONDO:0020779", "names": ["CHONDRODYSTROPHY", "chondrodystrophy", "Chondrodystrophy", "Cartilage deformed", "chondrodystrophies", "Chondrodystrophy NOS", "Chondrodystrophy, NOS", "Cartilage development disorder", "Cartilage Development Disorder", "cartilage development disorder", "Congenital anomaly of cartilage", "Abnormal development of cartilage", "abnormal development of cartilage", "Cartilage development disorder NOS", "DISORDER CARTILAGE DEVELOPMENT (NOS)", "Disorder cartilage development (NOS)", "Congenital anomaly of cartilage, NOS", "Abnormal development of cartilage, NOS", "Congenital anomaly of cartilage (disorder)", "Congenital anomaly of cartilage (diagnosis)", "congenital connective tissue disorder anomaly of cartilage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cartilage development disorder", "shortest_name_length": 16}
{"curie": "OMIM:111600", "names": [], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"]}
{"curie": "UMLS:C0751605", "names": ["familial spastic paraplegia x-linked", "X-linked hereditary spastic paraplegia", "X-Linked, Spastic Paraplegia, Hereditary", "X-linked hereditary spastic paraplegia (disorder)", "X-linked hereditary spastic paraplegia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-Linked, Spastic Paraplegia, Hereditary", "shortest_name_length": 36}
{"curie": "UMLS:C5419166", "names": ["COVID-19-Associated Encephalitis", "SARS-CoV-2 -Associated Encephalitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "COVID-19-Associated Encephalitis", "shortest_name_length": 32}
{"curie": "MONDO:0004615", "names": ["upper gum cancer", "gingiva of upper jaw cancer", "malignant tumor of upper gum", "malignant upper gum neoplasm", "Malignant tumor of upper gum", "Malignant tumour of upper gum", "malignant tumour of upper gum", "cancer of gingiva of upper jaw", "malignant neoplasm of upper gum", "Malignant neoplasm of upper gum", "Malignant tumor of upper gingiva", "malignant tumor of upper gingiva", "Malignant tumour of upper gingiva", "malignant gingiva of upper jaw neoplasm", "malignant neoplasm of gingiva of upper jaw", "Malignant tumor of upper gingiva (disorder)", "malignant neoplasm of upper gum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "upper gum cancer", "shortest_name_length": 16}
{"curie": "UMLS:C1333495", "names": ["Extra-Adrenal Retroperitoneal Paraganglioma", "Paraganglioma of Extra-Adrenal Retroperitoneal Area", "Paraganglioma of the Extra-Adrenal Retroperitoneal Area"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extra-Adrenal Retroperitoneal Paraganglioma", "shortest_name_length": 43}
{"curie": "MONDO:0011862", "names": ["SPG24", "spastic paraplegia 24", "hereditary spastic paraplegia 24", "hereditary spastic paraplegia type 24", "autosomal recessive spastic paraplegia 24", "Spastic Paraplegia 24, Autosomal Recessive", "spastic paraplegia 24, autosomal recessive", "SPASTIC PARAPLEGIA 24, AUTOSOMAL RECESSIVE", "autosomal recessive spastic paraplegia type 24", "Autosomal recessive spastic paraplegia type 24", "SPASTIC PARAPLEGIA 24, AUTOSOMAL RECESSIVE (disorder)", "Autosomal recessive spastic paraplegia type 24 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 24", "shortest_name_length": 5}
{"curie": "MONDO:0008737", "names": ["afibrinogenemia", "Afibrinogenemia", "AFIBRINOGENEMIA", "Afibrinogenaemia", "afibrinogenaemia", "Afibrinogenemias", "factor I deficiency", "Factor I deficiency", "fibrinogen deficiency", "Fibrinogen deficiency", "Familial Afibrinogenemia", "familial afibrinogenemia", "Familial afibrinogenemia", "Afibrinogenemia, Familial", "Familial Afibrinogenemias", "CONGENITAL AFIBRINOGENEMIA", "afibrinogenemia congenital", "Afibrinogenemias, Familial", "Afibrinogenemia (disorder)", "Congenital Afibrinogenemia", "congenital afibrinogenemia", "Congenital afibrinogenemia", "Congenital afibrinogenaemia", "Congenital Afibrinogenemias", "congenital; afibrinogenemia", "Afibrinogenemia, Congenital", "afibrinogenemia, congenital", "afibrinogenemia; congenital", "Congenital Afibrinogenaemia", "afibrinogenemia (diagnosis)", "AFIBRINOGENEMIA, CONGENITAL", "Congenital Afibrinogenaemias", "Afibrinogenaemia, Congenital", "Afibrinogenemias, Congenital", "Congenital Hypofibrinogenemia", "Hereditary hypofibrinogenemia", "Afibrinogenaemias, Congenital", "Congenital hypofibrinogenemia", "FACTOR I DEFICIENCY, COMPLETE", "Hypofibrinogenemia, Congenital", "HYPOFIBRINOGENEMIA, CONGENITAL", "hypofibrinogenemia; congenital", "congenital; hypofibrinogenemia", "hypofibrinogenemia, congenital", "Congenital Hypofibrinogenemias", "Hereditary hypofibrinogenaemia", "Congenital hypofibrinogenaemia", "Hypofibrinogenemias, Congenital", "Congenital afibrinogenemia (disorder)", "fibrinogen abnormality afibrinogenemia", "Congenital hypofibrinogenemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital afibrinogenemia", "shortest_name_length": 15}
{"curie": "UMLS:C1710166", "names": ["Sporadic Thyroid Gland Medullary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sporadic Thyroid Gland Medullary Carcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0015925", "names": ["ILD", "interstitial disease lung", "Interstitial lung disease", "LUNG DISEASE INTERSTITIAL", "lung interstitial disease", "disease interstitial lung", "interstitial lung disease", "Interstitial Lung Disease", "INTERSTITIAL LUNG DISEASE", "Interstitial Lung Diseases", "interstitial lung diseases", "lung diseases interstitial", "Lung Disease, Interstitial", "lung; disease, interstitial", "Lung Diseases, Interstitial", "ild interstitial lung disease", "Interstitial pulmonary disease", "ILD - Interstitial lung disease", "Diffuse parenchymal lung disease", "Diffuse Parenchymal Lung Disease", "Diffuse Parenchymal Lung Diseases", "Abnormal lung parenchyma morphology", "Interstitial lung disease (disorder)", "interstitial lung disease (diagnosis)", "Abnormal pulmonary interstitial morphology", "Interstitial pulmonary disease, unspecified", "Abnormality in area between air sacs in lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "interstitial lung disease", "shortest_name_length": 3}
{"curie": "UMLS:C4054590", "names": ["Lupus Flare"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lupus Flare", "shortest_name_length": 11}
{"curie": "MONDO:0003629", "names": ["uterine serous carcinoma", "endometrial serous adenocarcinoma", "uterine papillary serous carcinoma", "uterine corpus serous adenocarcinoma", "body of uterus serous adenocarcinoma", "uterine serous carcinoma/uterine papillary serous carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine corpus serous adenocarcinoma", "shortest_name_length": 24}
{"curie": "MONDO:0007329", "names": ["ICT", "ICC", "ETIC", "SEN SYNDROME", "Sen syndrome", "Cirrhosis, Familial", "CIRRHOSIS, FAMILIAL", "cirrhosis, familial", "Idiopathic cirrhosis", "cryptogenic cirrhosis", "Cryptogenic Cirrhosis", "Cryptogenic cirrhosis", "cirrhosis cryptogenic", "Cirrhosis, Cryptogenic", "CIRRHOSIS, CRYPTOGENIC", "cirrhosis, cryptogenic", "COPPER-OVERLOAD CIRRHOSIS", "Copper-Overload Cirrhosis", "copper-overload cirrhosis", "Indian childhood cirrhosis", "INDIAN CHILDHOOD CIRRHOSIS", "cirrhosis Indian childhood", "Indian Childhood Cirrhosis", "Indian childhood; cirrhosis", "cirrhosis; Indian childhood", "Cirrhosis, Indian childhood", "COPPER TOXICOSIS, IDIOPATHIC", "Copper Toxicosis, Idiopathic", "copper toxicosis, idiopathic", "hereditary cirrhosis of liver", "Cryptogenic cirrhosis (of liver)", "Cryptogenic cirrhosis (disorder)", "ICC - Indian childhood cirrhosis", "cryptogenic cirrhosis (diagnosis)", "ENDEMIC TYROLEAN INFANTILE CIRRHOSIS", "endemic Tyrolean infantile cirrhosis", "Endemic Tyrolean Infantile Cirrhosis", "Indian childhood cirrhosis (disorder)", "Indian childhood cirrhosis (diagnosis)", "CIRRHOSIS, NONCRYPTOGENIC, SUSCEPTIBILITY TO", "cirrhosis, Noncryptogenic, susceptibility to", "Cirrhosis-familial with pulmonary hypertension", "cirrhosis, familial, with pulmonary hypertension", "Cirrhosis, Familial, with Pulmonary Hypertension", "CIRRHOSIS, FAMILIAL, WITH PULMONARY HYPERTENSION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cirrhosis, familial", "shortest_name_length": 3}
{"curie": "MONDO:0010124", "names": ["THUMB, DISTAL HYPEREXTENSIBILITY OF", "thumb, distal hyperextensibility of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thumb, distal hyperextensibility of", "shortest_name_length": 35}
{"curie": "UMLS:C4520762", "names": ["Stage II Sinonasal Squamous Cell Carcinoma AJCC v6 and v7", "Stage II Nasal Cavity and Paranasal Sinus Squamous Cell Cancer", "Stage II Nasal Cavity and Paranasal Sinus Squamous Cell Carcinoma", "Stage II Nasal Cavity and Paranasal Sinus Squamous Cell Carcinoma AJCC v7", "Stage II Nasal Cavity and Paranasal Sinus Squamous Cell Carcinoma AJCC v6", "Stage II Nasal Cavity and Paranasal Sinus Squamous Cell Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Sinonasal Squamous Cell Carcinoma AJCC v6 and v7", "shortest_name_length": 57}
{"curie": "UMLS:C5419895", "names": ["Conventional Follicular Dendritic Cell Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conventional Follicular Dendritic Cell Sarcoma", "shortest_name_length": 46}
{"curie": "OMIM:601816", "names": ["BILIQTL1", "BILIRUBIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 8}
{"curie": "MONDO:0011655", "names": ["ASPS", "Alveolar Soft-Part Sarcoma", "Alveolar soft part sarcoma", "Alveolar soft-part sarcoma", "Alveolar Soft Part Sarcoma", "alveolar soft part sarcoma", "alveolar soft PART sarcoma", "alveolar soft-part sarcoma", "ALVEOLAR SOFT PART SARCOMA", "alveolar soft Part sarcoma", "alveolar; soft part sarcoma", "Alveolar soft part sarcomas", "Sarcoma, Alveolar Soft Part", "Alveolar soft tissue sarcoma", "alveolar soft tissue sarcoma", "sarcoma; alveolar, soft part", "alveolar soft-tissue sarcoma", "Alveolar soft part sarcoma NOS", "adult alveolar soft-part sarcoma", "Adult Alveolar Soft Part Sarcoma", "Adult Alveolar Soft-Part Sarcoma", "adult alveolar soft part sarcoma", "adult alveolar soft Part sarcoma", "adult alveolar soft-Part sarcoma", "alveolar soft-part sarcoma, adult", "sarcoma, alveolar soft-part, adult", "soft-part sarcoma, alveolar, adult", "childhood alveolar soft part sarcoma", "Pediatric Alveolar Soft Part Sarcoma", "pediatric alveolar soft-part sarcoma", "alveolar soft part sarcoma (disease)", "childhood alveolar soft-part sarcoma", "pediatric alveolar soft Part sarcoma", "Childhood Alveolar Soft-Part Sarcoma", "Childhood Alveolar Soft Part Sarcoma", "alveolar soft-part sarcoma, childhood", "alveolar soft-part sarcoma, pediatric", "Alveolar soft part sarcoma (disorder)", "alveolar soft part sarcoma (diagnosis)", "soft-part sarcoma, alveolar, childhood", "sarcoma, alveolar soft-part, pediatric", "sarcoma, alveolar soft-part, childhood", "soft-part sarcoma, alveolar, pediatric", "alveolar soft part sarcoma of soft tissue", "Alveolar soft part sarcoma (morphologic abnormality)", "alveolar soft part sarcoma of soft tissue (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alveolar soft part sarcoma", "shortest_name_length": 4}
{"curie": "UMLS:C0280362", "names": ["Stage IV Mouth Adenoid Cystic Carcinoma", "Stage IV Adenoid Cystic Carcinoma of Mouth", "Stage IV Oral Cavity Adenoid Cystic Cancer", "Stage IV Oral Cavity Adenoid Cystic Carcinoma", "Stage IV Adenoid Cystic Carcinoma of the Mouth", "oral cavity adenoid cystic carcinoma, stage IV", "Stage IV Adenoid Cystic Carcinoma of Oral Cavity", "oral cavity adenoid cystic carcinoma, metastatic", "Adenoid cystic carcinoma of the oral cavity stage IV", "stage IV adenoid cystic carcinoma of the oral cavity", "Stage IV Adenoid Cystic Carcinoma of the Oral Cavity", "Stage IV Oral Cavity Adenoid Cystic Carcinoma AJCC v7", "adenoid cystic carcinoma of the oral cavity, stage IV", "Stage IV Oral Cavity Adenoid Cystic Carcinoma AJCC v6", "metastatic adenoid cystic carcinoma of the oral cavity", "adenoid cystic carcinoma of the oral cavity, metastatic", "Stage IV Oral Cavity Adenoid Cystic Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenoid cystic carcinoma of the oral cavity stage IV", "shortest_name_length": 39}
{"curie": "MONDO:0007310", "names": ["Charcot-Marie-Tooth Disease, Guadalajara Neuronal Type", "Charcot-Marie-Tooth disease, Guadalajara neuronal type", "CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease, Guadalajara neuronal type", "shortest_name_length": 54}
{"curie": "MONDO:0009242", "names": ["BCS1", "EDS VIB (formerly)", "kyphoscoliosis type", "brittle cornea syndrome", "brittle cornea syndrome 1", "brittle cornea syndrome 2", "Ehlers-Danlos syndrome type 6b", "brittle cornea syndrome type 1", "type VIB Ehlers-Danlos syndrome", "Ehlers-Danlos syndrome type 6B (formerly)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brittle cornea syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C1262165", "names": ["High turnover osteopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High turnover osteopathy", "shortest_name_length": 24}
{"curie": "MONDO:0003196", "names": ["Ca appendix", "Appendix Cancer", "appendix cancer", "Appendiceal Cancer", "appendix carcinoma", "Appendix Carcinoma", "Appendix carcinoma", "Carcinoma of Appendix", "carcinoma of appendix", "Carcinoma of appendix", "carcinoma of the appendix", "Carcinoma of the appendix", "Carcinoma of the Appendix", "vermiform appendix carcinoma", "carcinoma of vermiform appendix", "carcinoma of appendix (diagnosis)", "Malignant epithelial neoplasm of appendix", "Malignant epithelial neoplasm of appendix (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "appendix carcinoma", "shortest_name_length": 11}
{"curie": "MONDO:0006589", "names": ["occupational eczema", "Occupational eczema", "industrial dermatitis", "Industrial dermatitis", "Occupational Dermatitis", "occupational dermatitis", "Dermatitis occupational", "dermatitis occupational", "Occupational dermatitis", "Dermatitis, Occupational", "Occupational Dermatitides", "Dermatitides, Occupational", "Occupational dermatitis (disorder)", "occupational allergic contact dermatitis", "Occupational allergic contact dermatitis", "occupational eczema (disorder) [ambiguous]", "Occupational allergic contact dermatitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "occupational dermatitis", "shortest_name_length": 19}
{"curie": "MONDO:0017771", "names": ["MRKH", "MRKH Syndrome", "MRKH syndrome", "Rokitansky syndrome", "Mullerian aplasia/dysgenesis", "Mullerian Aplasia/Dysgenesis", "Mayer-Rokitansky-Kuster-Hauser Syndrome", "Mayer-Rokitansky-Kuster-Hauser syndrome", "Mayer-Rokitansky-Küster-Hauser syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mayer-Rokitansky-Kuster-Hauser syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0156272", "names": ["enterovesical fistula", "Vesicoenteric fistula", "Enterovesical Fistula", "Enterovesical fistula", "Fistula, vesicoenteric", "Fistula, enterovesical", "fistula; vesicoenteric", "vesicoenteric; fistula", "Intestinovesical fistula", "Vesicointestinal fistula", "intestinovesical fistula", "fistula; vesicointestinal", "Vesico-intestinal fistula", "intestinovesical; fistula", "fistula; intestinovesical", "vesicointestinal; fistula", "enterovesical fistula (diagnosis)", "Intestinovesical fistula (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Enterovesical Fistula", "shortest_name_length": 21}
{"curie": "UMLS:C4721928", "names": ["stage IVA uterine sarcoma", "Stage IVA Uterine Sarcoma", "stage IVA uterine sarcoma AJCC v7", "Stage IVA Uterine Sarcoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Uterine Sarcoma AJCC v7", "shortest_name_length": 25}
{"curie": "MONDO:0019339", "names": ["47,XYY", "Y disomy", "Double Y", "disomy Y", "xyy trisomy", "XYY trisomy", "yy syndrome", "YY syndrome", "xyy syndrome", "XYY SYNDROME", "XYY Syndrome", "XYY syndrome", "XYY karyotype", "xyy karyotype", "karyotype xyy", "47 XYY syndrome", "47,XYY syndrome", "47,XYY Syndrome", "Jacob's syndrome", "47, XYY syndrome", "Double Y syndrome", "double y syndrome", "Karyotype 47, XYY", "double male syndrome", "47,XYY syndrome (diagnosis)", "Double Y syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "47,XYY syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C0238112", "names": ["Herpes esophagitis", "Herpes Esophagitis", "herpes esophagitis", "ESOPHAGITIS, HERPES", "herpes oesophagitis", "Herpes oesophagitis", "herpes esophagitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Herpes esophagitis", "shortest_name_length": 18}
{"curie": "MONDO:0008102", "names": ["SSS2", "SICK SINUS SYNDROME 2", "sick sinus syndrome 2", "Sss, autosomal dominant", "HCN4 sick sinus syndrome", "ATRIAL FIBRILLATION WITH BRADYARRHYTHMIA", "Atrial Fibrillation with Bradyarrhythmia", "atrial fibrillation with Bradyarrhythmia", "sick sinus syndrome 2, autosomal dominant", "Sick Sinus Syndrome 2, Autosomal Dominant", "sick sinus syndrome caused by mutation in HCN4", "Sinus Node Disease, Familial, Autosomal Dominant", "sinus node disease, familial, autosomal dominant", "SINUS NODE DISEASE, FAMILIAL, AUTOSOMAL DOMINANT", "SINUS BRADYCARDIA SYNDROME, FAMILIAL, AUTOSOMAL DOMINANT", "sinus bradycardia syndrome, familial, autosomal dominant", "Sinus Bradycardia Syndrome, Familial, Autosomal Dominant", "SICK SINUS SYNDROME 2 WITH OR WITHOUT CARDIAC NONCOMPACTION AND/OR ASCENDING AORTA DILATION", "sick sinus syndrome 2 with or without Cardiac noncompaction and/Or ascending aorta dilation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sick sinus syndrome 2, autosomal dominant", "shortest_name_length": 4}
{"curie": "MONDO:0022666", "names": ["cassavism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cassavism", "shortest_name_length": 9}
{"curie": "UMLS:C2981387", "names": ["Stage IIC Appendix Cancer", "Stage IIC Appendix Carcinoma", "Stage IIC Appendix Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIC Appendix Carcinoma AJCC v7", "shortest_name_length": 25}
{"curie": "UMLS:C0043246", "names": ["tear", "Torn", "torn", "Tear", "Rupture", "RUPTURE", "tearing", "rupture", "lacerate", "ruptured", "Ruptured", "ruptures", "Ruptures", "lacerates", "rupturing", "Tear, NOS", "lacerated", "Lacerated", "laceration", "LACERATION", "Laceration", "lacerating", "LACERATIONS", "lacerations", "Lacerations", "Tear - wound", "Rupture, NOS", "serious tear", "Laceration(s)", "lacerated wound", "Laceration, NOS", "Lacerated Wounds", "Wound, lacerated", "lacerated wounds", "injury laceration", "Laceration - injury", "laceration (diagnosis)", "Laceration - injury (disorder)", "Rupture (morphologic abnormality)", "Laceration (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laceration", "shortest_name_length": 4}
{"curie": "UMLS:C1332212", "names": ["B Lymphoblastic Lymphoma", "Adult B-Lymphoblastic Lymphoma", "Adult B Lymphoblastic Lymphoma", "Adult Precursor B-Lymphoblastic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult B Lymphoblastic Lymphoma", "shortest_name_length": 24}
{"curie": "MONDO:0025062", "names": ["Talfan disease", "disease, Talfan", "Teschen disease", "disease, Teschen", "Porcine Poliomyelitis", "porcine poliomyelitis", "poliomyelitis, porcine", "Poliomyelitis, Porcine", "Enzootic Porcine Encephalomyelitis", "enzootic porcine encephalomyelitis", "porcine encephalomyelitis, enzootic", "Encephalomyelitis, Enzootic Porcine", "encephalomyelitis, enzootic porcine", "Porcine Encephalomyelitis, Enzootic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephalomyelitis, enzootic porcine", "shortest_name_length": 14}
{"curie": "MONDO:0004614", "names": ["LEUKEMIA MONOCYTIC CHRONIC", "Chronic Monocytic Leukemia", "Leukemia monocytic chronic", "leukemia monocytic chronic", "CHRONIC MONOCYTIC LEUKEMIA", "chronic monocytic leukemia", "Chronic monocytic leukemia", "Chronic monocytoid leukemia", "Monocytic Leukemia, Chronic", "Leukaemia monocytic chronic", "Chronic monocytic leukaemia", "Chronic Monocytic Leukemias", "Leukemia, Chronic Monocytic", "monocytic leukemia, chronic", "Monocytic leukemia, chronic", "monocytic; leukemia, chronic", "Leukemia, Monocytic, Chronic", "Monocytic Leukemias, Chronic", "Leukemias, Chronic Monocytic", "Monocytic leukaemia, chronic", "[M]Chronic monocytic leukemia", "[M]Chronic monocytic leukaemia", "Chronic monocytic leukemia (disorder)", "chronic monocytic leukemia (diagnosis)", "Chronic monocytic leukemia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic monocytic leukemia", "shortest_name_length": 26}
{"curie": "MONDO:0020449", "names": ["persistent eustachian valve"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "persistent eustachian valve", "shortest_name_length": 27}
{"curie": "UMLS:C4331229", "names": ["Recurrent Glioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Glioma", "shortest_name_length": 16}
{"curie": "MONDO:0004800", "names": ["chronic dacryoadenitis", "Chronic dacryoadenitis", "dacryoadenitis, chronic", "Chronic dacryoadenitis (disorder)", "chronic dacryoadenitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic dacryoadenitis", "shortest_name_length": 22}
{"curie": "MONDO:0013415", "names": ["17p13.1 deletion syndrome", "Agyria-Pachygyria-Band Spectrum", "Agyria Pachygyria Band Spectrum", "chromosome 17p13.1 deletion syndrome", "CHROMOSOME 17p13.1 DELETION SYNDROME", "Lissencephaly Subcortical Band Heterotopia", "Lissencephaly-Subcortical Band Heterotopia", "Band Heterotopia, Lissencephaly-Subcortical", "Heterotopia, Lissencephaly-Subcortical Band", "Lissencephaly-Subcortical Band Heterotopias", "Heterotopias, Lissencephaly-Subcortical Band", "Classical Lissencephalies and Subcortical Band Heterotopias"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 17p13.1 deletion syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0015084", "names": ["FRAXF syndrome", "FRAXF syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FRAXF syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C4682933", "names": ["IIIB", "stage IIIB bladder cancer", "Stage IIIB Bladder Cancer", "stage IIIB bladder cancer AJCC v8", "Stage IIIB Bladder Cancer AJCC v8", "stage IIIB bladder carcinoma AJCC v8", "Stage IIIB Bladder Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Bladder Cancer AJCC v8", "shortest_name_length": 4}
{"curie": "UMLS:C0333106", "names": ["varice bleed", "bleeding varices", "Bleeding varices", "variceal hemorrhage", "BLEEDING VARICOSE VEIN", "Bleeding varicose vein", "bleeding varicose veins", "Varicose vein hemorrhage", "Varicose vein haemorrhage", "Bleeding varices (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bleeding varices", "shortest_name_length": 12}
{"curie": "MONDO:0009396", "names": ["HYPERPARATHYROIDISM, NEONATAL SELF-LIMITED PRIMARY, WITH HYPERCALCIURIA", "hyperparathyroidism, neonatal self-limited primary, with hypercalciuria", "Hyperparathyroidism, Neonatal Self-Limited Primary, With Hypercalciuria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperparathyroidism, neonatal self-limited primary, with hypercalciuria", "shortest_name_length": 71}
{"curie": "MONDO:0010596", "names": ["Mesangiocapillary glomerulonephritis, X-linked", "Mesangiocapillary Glomerulonephritis, X-Linked", "MESANGIOCAPILLARY GLOMERULONEPHRITIS, X-LINKED", "Membranoproliferative Glomerulonephritis, X-Linked", "MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS, X-LINKED", "membranoproliferative glomerulonephritis, X-linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "membranoproliferative glomerulonephritis, X-linked", "shortest_name_length": 46}
{"curie": "MONDO:0013474", "names": ["CMH17", "hypertrophic cardiomyopathy 17", "cardiomyopathy, hypertrophic, 17", "JPH2 hypertrophic cardiomyopathy", "hypertrophic cardiomyopathy type 17", "cardiomyopathy familial hypertrophic 17", "CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC 17", "cardiomyopathy, familial hypertrophic, 17", "CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 17", "Familial Hypertrophic Cardiomyopathy Type 17", "cardiomyopathy, familial hypertrophic, type 17", "hypertrophic cardiomyopathy caused by mutation in JPH2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophic cardiomyopathy 17", "shortest_name_length": 5}
{"curie": "MONDO:0020468", "names": ["UPD(13)pat", "paternal uniparental disomy of chromosome 13", "paternal uniparental disomy of chromosome type 13"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paternal uniparental disomy of chromosome 13", "shortest_name_length": 10}
{"curie": "MONDO:0020156", "names": ["syndromic ankyloblepharon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic ankyloblepharon", "shortest_name_length": 25}
{"curie": "MONDO:0033717", "names": ["congenital cerebellar ataxia due to RNU12 mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital cerebellar ataxia due to RNU12 mutation", "shortest_name_length": 50}
{"curie": "MONDO:0003193", "names": ["Adenocarcinoma", "Bile duct adenocarcinoma", "Bile Duct Adenocarcinoma", "bile duct adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bile duct adenocarcinoma", "shortest_name_length": 14}
{"curie": "UMLS:C0009439", "names": ["common bile duct cyst", "Common Bile Duct Cyst", "bile common cyst duct", "cysts common bile duct", "Cyst, Common Bile Duct", "choledochal cyst i type", "Cysts, Common Bile Duct", "Choledochal Cyst, Type I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Choledochal Cyst, Type I", "shortest_name_length": 21}
{"curie": "MONDO:0031432", "names": ["thyroid hormone metabolism, abnormal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid hormone metabolism, abnormal", "shortest_name_length": 36}
{"curie": "MONDO:0014377", "names": ["DEE24", "EIEE24", "early infantile epileptic encephalopathy 24", "developmental and epileptic encephalopathy 24", "epileptic encephalopathy, early infantile, 24", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 24", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 24", "HCN1 early infantile epileptic encephalopathy", "developmental and epileptic encephalopathy, 24", "epileptic encephalopathy, early infantile, type 24", "early infantile epileptic encephalopathy caused by mutation in HCN1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 24", "shortest_name_length": 5}
{"curie": "MONDO:0009911", "names": ["Hypoprolactinemia", "hypoprolactinemia", "Hypoprolactinaemia", "hypoprolactinaemia", "Prolactin deficiency", "prolactin deficiency", "Prolactin Deficiency", "Isolated prolactin deficiency", "Lactogenic Hormone Deficiency", "Prolactin Deficiency, Isolated", "PROLACTIN DEFICIENCY, ISOLATED", "prolactin deficiency, isolated", "prolactin deficiency (diagnosis)", "Isolated prolactin deficiency (disorder)", "Reduced circulating prolactin concentration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prolactin deficiency, isolated", "shortest_name_length": 17}
{"curie": "MONDO:0007746", "names": ["OHDS", "hyperbradykininism", "HYPERBRADYKININISM", "Hyperbradykininism", "ORTHOSTATIC HYPOTENSIVE DISORDER", "orthostatic hypotensive disorder", "Orthostatic Hypotensive Disorder", "orthostatic hypotensive disorder of Streeten", "ORTHOSTATIC HYPOTENSIVE DISORDER, STREETEN TYPE", "Orthostatic Hypotensive Disorder, Streeten Type", "orthostatic hypotensive disorder, Streeten type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orthostatic hypotensive disorder, Streeten type", "shortest_name_length": 4}
{"curie": "UMLS:C0559487", "names": ["Paratesticular Tumor", "Paratesticular tumor", "Paratesticular tumour", "Paratesticular Neoplasm", "Paratesticular tumor (disorder)", "Tumor of Paratesticular Structures", "Neoplasm of Paratesticular Structures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paratesticular tumor", "shortest_name_length": 20}
{"curie": "MONDO:0015366", "names": ["autosomal recessive hereditary sensory and autonomic neuropathy", "hereditary sensory and autonomic neuropathy, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive hereditary sensory and autonomic neuropathy", "shortest_name_length": 63}
{"curie": "UMLS:C0038441", "names": ["stress disorder", "stress disorders", "Stress disorders", "disorder; stress", "stress; disorder", "Traumatic Stress Disorder", "traumatic stress disorder", "Traumatic Stress Disorders", "Stress Disorder, Traumatic", "Stress Disorders, Traumatic", "stress disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stress Disorders, Traumatic", "shortest_name_length": 15}
{"curie": "MONDO:0009098", "names": ["Aughton syndrome", "DEXTROCARDIA WITH UNUSUAL FACIES AND MICROPHTHALMIA", "Dextrocardia with unusual facies and microphthalmia", "dextrocardia with unusual facies and microphthalmia", "Dextrocardia, microphthalmia, cleft palate, and mental retardation", "dextrocardia, microphthalmia, cleft palate, choreoathetosis and mental retardation", "dextrocardia, microphthalmia, cleft palate, choreoathetosis and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dextrocardia with unusual facies and microphthalmia", "shortest_name_length": 16}
{"curie": "MONDO:0019342", "names": ["SCKL", "Seckel", "Seckel nanism", "Seckel syndrome", "Seckel Syndrome", "seckel syndrome", "seckels syndrome", "Seckel's syndrome", "Harper's syndrome", "Bird-headed dwarf", "seckel's syndrome", "Nanocephalic dwarf", "Dwarf, nanocephalic", "Seckel-type Dwarfism", "Seckel-Type Dwarfism", "bird-headed dwarfism", "Bird-Headed Dwarfism", "Seckel syndrome (SS)", "Seckel-type dwarfism", "nanocephalic dwarfism", "Nanocephalic Dwarfism", "nanocephalic Dwarfism", "microcephalic dwarfism", "birdlike face syndrome", "Virchow-Seckel syndrome", "Virchow-Seckel dwarfism", "Seckel bird head syndrome", "seckel bird head syndrome", "Seckel syndrome (disorder)", "Bird-headed dwarf of Seckel", "Seckel syndrome (diagnosis)", "familial bird-headed dwarfism", "microcephalic primordial dwarfism", "Microcephalic Primordial Dwarfism", "Microcephalic primordial dwarfism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Seckel syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C5420049", "names": ["Sinonasal Malignant Peripheral Nerve Sheath Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Malignant Peripheral Nerve Sheath Tumor", "shortest_name_length": 49}
{"curie": "MONDO:0009032", "names": ["CED", "CED1", "Levin syndrome", "LEVIN SYNDROME I", "Levin Syndrome I", "Levin syndrome I", "Sensenbrenner syndrome", "SENSENBRENNER SYNDROME", "Sensenbrenner Syndrome", "Sensenbrenner's syndrome", "cranioectodermal dysplasia", "Cranioectodermal dysplasia", "Cranioectodermal Dysplasia", "cranio-ectodermal dysplasia", "CRANIOECTODERMAL DYSPLASIA 1", "cranio-ectodermal dysplasia (CED)", "Sensenbrenner-Dorst-Owens syndrome", "Cranioectodermal dysplasia (disorder)", "tooth anomalies-skeletal-dysplasia-sparse hair syndrome", "skeletal dysplasia-sparse hair-dental anomalies syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cranioectodermal dysplasia", "shortest_name_length": 3}
{"curie": "MONDO:0002172", "names": ["EUSTACHITIS", "Eustachitis", "OTOSALPINGITIS", "Otosalpingitis", "otosalpingitis", "Tubotympanitis", "rhinosalpingitis", "Tubotympanitis, NOS", "Otosalpingitis, NOS", "Eustachian salpingitis", "eustachian salpingitis", "Salpingitis;eustachian", "Eustachian salpingitis, NOS", "Eustachian tube salpingitis", "salpingitis; eustachian tube", "eustachian tube; salpingitis", "inflammation; eustachian tube", "eustachian tube; inflammation", "inflammation of eustachian tube", "eustachian salpingitis (diagnosis)", "Unspecified Eustachian salpingitis", "pharyngotympanic tube inflammation", "Eustachian salpingitis, unspecified", "inflammation of pharyngotympanic tube", "Eustachian tube salpingitis (disorder)", "Unspecified Eustachian salpingitis, unspecified ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "otosalpingitis", "shortest_name_length": 11}
{"curie": "MONDO:0011533", "names": ["TPBS", "TEMTAMY PREAXIAL BRACHYDACTYLY SYNDROME", "TEMTAMY preaxial brachydactyly syndrome", "temtamy preaxial brachydactyly syndrome", "Temtamy preaxial brachydactyly syndrome", "Preaxial brachydactyly syndrome, Temtamy type", "PREAXIAL BRACHYDACTYLY SYNDROME, TEMTAMY TYPE", "preaxial brachydactyly syndrome, Temtamy type", "preaxial brachydactyly syndrome, TEMTAMY type", "Temtamy preaxial brachydactyly syndrome (disorder)", "temtamy preaxial brachydactyly syndrome (diagnosis)", "mental retardation syndrome with preaxial brachydactyly, hyperphalangism, deafness and orodental anomalies", "intellectual disability syndrome with preaxial brachydactyly, hyperphalangism, deafness and orodental anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "temtamy preaxial brachydactyly syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0006505", "names": ["Basal Ganglia Vascular Disease", "Vascular Disease, Basal Ganglia", "Vascular Diseases, Basal Ganglia", "Basal Ganglia Cerebrovascular Disease", "basal ganglia cerebrovascular disease", "Cerebrovascular Disease, Basal Ganglia", "basal ganglia cerebrovascular disorder", "collection of basal ganglia cerebrovascular disorder", "cerebrovascular disorder of collection of basal ganglia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "basal ganglia cerebrovascular disorder", "shortest_name_length": 30}
{"curie": "MONDO:0010297", "names": ["FGS2", "FG SYNDROME 2", "FG syndrome 2", "FLNA FG syndrome", "FG syndrome type 2", "FG syndrome caused by mutation in FLNA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FG syndrome 2", "shortest_name_length": 4}
{"curie": "MONDO:0019572", "names": ["ARCL1", "cutis laxa, type 1", "Cutis laxa, type 1", "Cutis laxa, recessive", "Cutis laxa, recessive, type I", "autosomal recessive cutis laxa type I", "autosomal recessive cutis laxa type 1", "cutis laxa, autosomal recessive type 1", "Cutis laxa, recessive, type I (disorder)", "autosomal recessive cutis laxa, pulmonary emphysema type", "autosomal recessive cutis laxa with severe systemic involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive cutis laxa type 1", "shortest_name_length": 5}
{"curie": "MONDO:0016601", "names": ["late-onset citrullinemia type I", "late-onset citrullinemia type 1", "adult-onset citrullinemia type I", "adult-onset citrullinemia type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult-onset citrullinemia type I", "shortest_name_length": 31}
{"curie": "UMLS:C1710609", "names": ["Vaginal Angiomyofibroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Angiomyofibroblastoma", "shortest_name_length": 29}
{"curie": "MONDO:0019557", "names": ["CHLE", "CHBL1", "Chilblain lupus", "CHILBLAIN LUPUS", "chilblain lupus", "Hutchinson lupus", "CHILBLAIN LUPUS 1", "Chilblain lupus 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chilblain lupus", "shortest_name_length": 4}
{"curie": "MONDO:0010924", "names": ["D2HA", "D2HGA", "D-2-HGA", "D-2(OH) glutaric aciduria", "D-2-Hydroxyglutaric Acidemia", "D-2-hydroxyglutaric aciduria", "D-2-hydroxyglutaric acidemia", "D-2-hydroxyglutaric aciduria 1", "D-2-hydroxyglutaric aciduria type 1", "D-2-hydroxyglutaric aciduria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "D-2-hydroxyglutaric aciduria", "shortest_name_length": 4}
{"curie": "MONDO:0017488", "names": ["ulnar hemimelia, bilateral", "ulnar longitudinal meromelia, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ulnar hemimelia, bilateral", "shortest_name_length": 26}
{"curie": "UMLS:C1868758", "names": ["Superinfection bacterial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Superinfection bacterial", "shortest_name_length": 24}
{"curie": "MONDO:0011360", "names": ["DFNB14", "autosomal recessive deafness 14", "Deafness, Autosomal Recessive 14", "DEAFNESS, AUTOSOMAL RECESSIVE 14", "deafness, autosomal recessive 14", "autosomal recessive nonsyndromic deafness 14", "autosomal recessive nonsyndromic hearing loss 14", "autosomal recessive nonsyndromic deafness type 14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 14", "shortest_name_length": 6}
{"curie": "UMLS:C4683585", "names": ["Lugano Classification Limited Stage Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Limited Stage Hodgkin Lymphoma AJCC v8", "shortest_name_length": 60}
{"curie": "MONDO:0005192", "names": ["Pancreas Cancer", "exocrine cancer", "pancreas cancer", "PANCREATIC CANCER", "pancreatic cancer", "Pancreatic Cancer", "Cancer of Pancreas", "carcinoma pancreas", "Pancreas Carcinoma", "pancreas carcinoma", "Carcinoma;pancreas", "PANCREAS CARCINOMA", "Pancreas carcinoma", "cancer of pancreas", "PANCREATIC CARCINOMA", "Pancreatic carcinoma", "carcinoma pancreatic", "pancreatic carcinoma", "Pancreatic Carcinoma", "Carcinoma of pancreas", "CARCINOMA OF PANCREAS", "Carcinoma of Pancreas", "carcinoma of pancreas", "cancer of the pancreas", "Cancer of the Pancreas", "Pancreatic carcinoma NOS", "carcinoma of the pancreas", "Carcinoma of the Pancreas", "exocrine pancreas carcinoma", "Exocrine Pancreas Carcinoma", "PANCREATIC ACINAR CARCINOMA", "Exocrine pancreas carcinoma", "Pancreatic Acinar Carcinoma", "exocrine pancreatic carcinoma", "pancreatic carcinoma, familial", "Pancreatic cancer (not Islets)", "pancreatic cancer (not islets)", "carcinoma of exocrine pancreas", "Pancreatic carcinoma, familial", "Carcinoma of pancreas (disorder)", "carcinoma of pancreas (diagnosis)", "Pancreatic cancer (excluding Islets), NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exocrine pancreatic carcinoma", "shortest_name_length": 15}
{"curie": "MONDO:0008201", "names": ["Perry Syndrome", "PERRY SYNDROME", "Perry syndrome", "Perry syndrome (disorder)", "Parkinsonism with alveolar hypoventilation and mental depression", "PARKINSONISM WITH ALVEOLAR HYPOVENTILATION AND MENTAL DEPRESSION", "Parkinsonism with Alveolar Hypoventilation and Mental Depression", "parkinsonism with alveolar hypoventilation and mental depression"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perry syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C0015786", "names": ["female sexual arousal disorder", "Female Sexual Arousal Disorder", "Female sexual arousal disorder", "sexual; disorder, arousal, female", "disorder; sexual, arousal, female", "Female sexual arousal disorder (disorder)", "female sexual arousal disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Female sexual arousal disorder", "shortest_name_length": 30}
{"curie": "UMLS:C0334113", "names": ["Inflammatory Fibroid Polyp", "Inflammatory fibroid polyp", "Eosinophilic granulomatous polyp", "Polyp, eosinophilic granulomatous", "Eosinophilic granulomatous polyp (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eosinophilic granulomatous polyp", "shortest_name_length": 26}
{"curie": "MONDO:0015482", "names": ["otomandibular dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "otomandibular dysplasia", "shortest_name_length": 23}
{"curie": "UMLS:C0278772", "names": ["Resectable Liver Cancer", "Localized Resectable Adult Liver Cancer", "Localized Resectable Adult Liver Carcinoma", "Localized Resectable Adult Primary Liver Cancer", "localized resectable adult primary liver cancer", "liver cancer, localized resectable adult primary", "adult primary liver cancer, localized resectable", "Localized Resectable Adult Primary Cancer of Liver", "Localized Resectable Adult Primary Cancer of the Liver"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized Resectable Adult Liver Carcinoma", "shortest_name_length": 23}
{"curie": "MONDO:0001535", "names": ["Vagus Neuropathy", "Neuropathy, Vagus", "n.vagus; disorder", "Vagus Neuropathies", "Vagus nerve lesion", "Neuropathies, Vagus", "Vagus Nerve Disease", "Vagus nerve disease", "disease vagus nerve", "vagus nerve disease", "Vagus Nerve Diseases", "disorder vagus nerve", "vagus nerve disorder", "Vagus nerve disorder", "Vagus Nerve Disorder", "Vagus Nerve Disorders", "vagus nerve disorders", "Vagus nerve disorders", "disease of vagus nerve", "disorder of vagal nerve", "Disorders of 10th nerve", "disorder of vagus nerve", "Disorder of vagus nerve", "Disorders of vagus nerve", "Vagus nerve disorder NOS", "Cranial Nerve X Diseases", "Disorders of vagal nerve", "n.pneumogastric; disorder", "Tenth cranial nerve disorder", "Disorders of the tenth nerve", "Tenth Cranial Nerve Diseases", "Pneumogastric Nerve Disorder", "Disorder of vagus nerve, NOS", "Disorder of cranial nerve 10", "Pneumogastric Nerve Disorders", "Disorder, Pneumogastric Nerve", "Disorders, Pneumogastric Nerve", "Disorder of pneumogastric nerve", "Vagus nerve disease or syndrome", "vagus nerve disease or disorder", "Disorders of pneumogastric nerve", "disease or disorder of vagus nerve", "Disorders of the Xth cranial nerve", "Disorder of vagus nerve (disorder)", "Disorder of the tenth cranial nerve", "disorder of vagus nerve (diagnosis)", "disease (or disorder); nerve, vagus", "Disorder of pneumogastric nerve, NOS", "disorder of pneumogastric [10th] nerve", "cranial nerve; disorder, tenth (vagus)", "Tenth cranial nerve disease or syndrome", "Disorders of pneumogastric [10th] nerve", "Disorder of the tenth cranial nerve, NOS", "disease (or disorder); nerve, pneumogastric", "disease (or disorder); cranial nerve, tenth (vagus)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vagus nerve disorder", "shortest_name_length": 16}
{"curie": "MONDO:0100213", "names": ["IFAP1", "IFAP syndrome", "IFAP syndrome 1", "IFAP SYNDROME 1", "IFAP/BRESHECK syndrome", "IFAP syndrome with or without BRESHECK syndrome", "Ifap syndrome with or without Bresheck syndrome", "IFAP syndrome 1 with or without BRESHECK syndrome", "IFAP SYNDROME 1, WITH OR WITHOUT BRESHECK SYNDROME", "ichthyosis follicularis-atrichia-photophobia syndrome", "Ichthyosis follicularis-atrichia-photophobia syndrome", "ichthyosis follicularis-alopecia-photophobia syndrome", "Ichthyosis follicularis atrichia photophobia syndrome", "ichthyosis follicularis atrichia photophobia syndrome", "Ichthyosis follicularis-alopecia-photophobia syndrome", "ichthyosis follicularis-atrichia-photophobia syndrome 1", "ichthyosis follicularis-alopecia-photophobia syndrome 1", "Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome", "IFAP syndrome with or without BRESHECK syndrome, X-linked recessive", "IFAP syndrome Ichthyosis follicularis atrichia photophobia syndrome", "ichthyosis follicularis, atrichia, and photophobia with or without brain anomalies, retardation, ectodermal dysplasia, skeletal malformations, Hirschsprung disease, Ear/eye anomalies, cleft palate/cryptorchidism, and kidney dysplasia/hypoplasia", "ICHTHYOSIS FOLLICULARIS, ATRICHIA, AND PHOTOPHOBIA WITH OR WITHOUT BRAIN ANOMALIES, RETARDATION, ECTODERMAL DYSPLASIA, SKELETAL MALFORMATIONS, HIRSCHSPRUNG DISEASE, EAR/EYE ANOMALIES, CLEFT PALATE/CRYPTORCHIDISM, AND KIDNEY DYSPLASIA/HYPOPLASIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IFAP syndrome with or without BRESHECK syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0003216", "names": ["Ureter Adenocarcinoma", "ureter adenocarcinoma", "Ureteral Adenocarcinoma", "ureteral adenocarcinoma", "Adenocarcinoma of Ureter", "adenocarcinoma of ureter", "adenocarcinoma of the ureter", "Adenocarcinoma of the Ureter", "adenocarcinoma of ureter (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ureter adenocarcinoma", "shortest_name_length": 21}
{"curie": "MONDO:0003293", "names": ["Lung Leiomyoma", "lung leiomyoma", "Leiomyoma of Lung", "leiomyoma of lung", "Leiomyoma of lung", "Pulmonary Leiomyoma", "Pulmonary leiomyoma", "pulmonary leiomyoma", "leiomyoma of the lung", "Leiomyoma of the Lung", "Leiomyoma of lung (disorder)", "leiomyoma of lung (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung leiomyoma", "shortest_name_length": 14}
{"curie": "UMLS:C5555673", "names": ["Untreated Prolymphocytic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Untreated Prolymphocytic Leukemia", "shortest_name_length": 33}
{"curie": "MONDO:0001818", "names": ["NEURALGIA FACIAL", "facial neuralgia", "Facial neuralgia", "Facial Neuralgia", "Neuralgia facial", "facial neuralgias", "Neuralgia, Facial", "Facial Neuralgias", "Neuralgias, Facial", "facial pain syndrome", "face; pain, syndrome", "Facial neuralgia NOS", "Facial Pain Syndrome", "Pain Syndrome, Facial", "Facial Pain Syndromes", "facial pain; syndrome", "syndrome; facial pain", "Syndrome, Facial Pain", "Pain Syndromes, Facial", "facial nerve neuralgia", "Syndromes, Facial Pain", "neuralgia of facial nerve", "Facial neuralgia (finding)", "Craniofacial Pain Syndrome", "Syndrome, Craniofacial Pain", "Craniofacial Pain Syndromes", "Pain Syndrome, Craniofacial", "Syndromes, Craniofacial Pain", "Pain Syndromes, Craniofacial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "facial neuralgia", "shortest_name_length": 16}
{"curie": "UMLS:C1518226", "names": ["Malignant Non-Hodgkin's Lymphoma, Diffuse, Lymphocytic, Poorly Differentiated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Non-Hodgkin's Lymphoma, Diffuse, Lymphocytic, Poorly Differentiated", "shortest_name_length": 77}
{"curie": "UMLS:C0241558", "names": ["urethrorrhagia", "Urethrorrhagia", "urethra bleeding", "bleeding urethra", "Bleeding-urethral", "Urethral bleeding", "URETHRAL BLEEDING", "urethral bleeding", "URETHRA HEMORRHAGE", "Urethral Hemorrhage", "Urethral hemorrhage", "hemorrhage; urethra", "urethra; hemorrhage", "Urethral haemorrhage", "bleeding from urethra", "Bleeding from urethra", "Hemorrhage of urethra", "Haemorrhage of urethra", "Bleeding from urethra (finding)", "Hemorrhage of urethra (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemorrhage of urethra", "shortest_name_length": 14}
{"curie": "UMLS:C4525463", "names": ["Pancreatic Cancer by AJCC v6 and v7 Stage", "Pancreatic Carcinoma by AJCC v6 and v7 Stage", "Exocrine and Endocrine Pancreatic Cancer by AJCC v6 and v7 Stage", "Exocrine and Endocrine Pancreatic Carcinoma by AJCC v6 and v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Cancer by AJCC v6 and v7 Stage", "shortest_name_length": 41}
{"curie": "MONDO:0018086", "names": ["type of genodermatosis", "ulerythema ophryogenesis", "keratosis pilaris affecting the follicles of the eyebrow hairs"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ulerythema ophryogenesis", "shortest_name_length": 22}
{"curie": "MONDO:0014295", "names": ["SPG57", "hereditary spastic paraplegia 57", "TFG hereditary spastic paraplegia", "hereditary spastic paraplegia type 57", "autosomal recessive spastic paraplegia 57", "SPASTIC PARAPLEGIA 57, AUTOSOMAL RECESSIVE", "spastic paraplegia 57, autosomal recessive", "autosomal recessive spastic paraplegia type 57", "Autosomal recessive spastic paraplegia type 57", "Spastic paraplegia due to partial TFG deficiency", "spastic paraplegia due to partial TFG deficiency", "hereditary spastic paraplegia caused by mutation in TFG", "familial spastic paraplegia autosomal recessive type 57", "Autosomal recessive spastic paraplegia type 57 (disorder)", "Autosomal recessive spastic paraplegia type 57 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 57", "shortest_name_length": 5}
{"curie": "MONDO:0008934", "names": ["cerebellar ataxia ectodermal dysplasia", "Cerebellar ataxia ectodermal dysplasia", "cerebellar ataxia - ectodermal dysplasia", "Ectodermal dysplasia and cerebellar ataxia", "cerebellar ataxia and ectodermal dysplasia", "Cerebellar Ataxia and Ectodermal Dysplasia", "Cerebellar ataxia and ectodermal dysplasia", "ectodermal dysplasia and cerebellar ataxia", "CEREBELLAR ATAXIA AND ECTODERMAL DYSPLASIA", "Cerebellar ataxia-ectodermal dysplasia syndrome", "cerebellar ataxia-ectodermal dysplasia syndrome", "Cerebellar ataxia co-occurrent with ectodermal dysplasia", "Cerebellar ataxia co-occurrent with ectodermal dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellar ataxia-ectodermal dysplasia syndrome", "shortest_name_length": 38}
{"curie": "MONDO:0009545", "names": ["McAlister Coe Whyte syndrome", "McAlister coe Whyte syndrome", "Macroepiphyseal dysplasia, McAlister coe type", "Macroepiphyseal dysplasia, McAlister Coe type", "MACROEPIPHYSEAL DYSPLASIA WITH OSTEOPOROSIS, WRINKLED SKIN, AND AGED APPEARANCE", "macroepiphyseal dysplasia with osteoporosis, wrinkled skin, and aged appearance", "Macroepiphyseal Dysplasia with Osteoporosis, Wrinkled Skin, and Aged Appearance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macroepiphyseal dysplasia with osteoporosis, wrinkled skin, and aged appearance", "shortest_name_length": 28}
{"curie": "MONDO:0013210", "names": ["DFNB25", "autosomal recessive deafness 25", "DEAFNESS, AUTOSOMAL RECESSIVE 25", "deafness, autosomal recessive 25", "deafness, autosomal recessive type 25", "autosomal recessive nonsyndromic deafness 25", "GRXCR1 autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 25", "autosomal recessive nonsyndromic deafness type 25", "autosomal recessive nonsyndromic deafness caused by mutation in GRXCR1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 25", "shortest_name_length": 6}
{"curie": "UMLS:C5420033", "names": ["Sinonasal Neuroendocrine Carcinoma", "Nasal Cavity and Paranasal Sinus Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Neuroendocrine Carcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0015580", "names": ["Monosomy 7qter", "monosomy 7qter", "Distal monosomy 7q36", "Distal deletion 7q36", "distal deletion 7q36", "distal monosomy 7q36", "telomeric deletion 7q36", "Telomeric deletion 7q36", "distal monosomy type 7q36", "Distal monosomy 7q36 syndrome", "Distal monosomy 7q36 syndrome (disorder)", "Distal monosomy 7q36 syndrome (diagnosis)", "deletion of part of chromosome 7 distal monosomy 7q36 syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal monosomy 7q36", "shortest_name_length": 14}
{"curie": "MONDO:0008456", "names": ["Spinocerebellar Ataxia With Rigidity And Peripheral Neuropathy", "SPINOCEREBELLAR ATAXIA WITH RIGIDITY AND PERIPHERAL NEUROPATHY", "spinocerebellar ataxia with rigidity and peripheral neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia with rigidity and peripheral neuropathy", "shortest_name_length": 62}
{"curie": "MONDO:0011617", "names": ["ARTHROPATHY, EROSIVE", "Arthropathy, Erosive", "arthropathy, erosive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthropathy, erosive", "shortest_name_length": 20}
{"curie": "UMLS:C0481408", "names": ["Personality, psychoneurotic", "Psychoneurotic personality disorder", "psychoneurotic personality disorder", "personality disorder; psychoneurotic", "psychoneurotic; personality disorder", "Psychoneurotic personality disorder (disorder)", "psychoneurotic personality disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Psychoneurotic personality disorder", "shortest_name_length": 27}
{"curie": "MONDO:0002527", "names": ["keratoacanthoma", "Keratoacanthoma", "KERATOACANTHOMA", "Keratoacanthomas", "keratoacanthomas", "Molluscum sebaceum", "KA - Keratoacanthoma", "Keratoacanthoma, NOS", "Skin Keratoacanthoma", "Cutaneous Keratoacanthoma", "Keratoacanthoma (disorder)", "keratoacanthoma (diagnosis)", "Squamous cell carcinoma, keratoacanthoma-type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratoacanthoma", "shortest_name_length": 15}
{"curie": "MONDO:0002693", "names": ["lateral sinus thrombosis", "Lateral Sinus Thrombosis", "Lateral Sinus Thromboses", "Thrombosis, Lateral Sinus", "Thromboses, Lateral Sinus", "THROMBOSIS, LATERAL SINUS", "thrombosis transverse sinus", "Transverse Sinus Thrombosis", "Thrombosis transverse sinus", "Transverse sinus thrombosis", "Transverse Sinus Thromboses", "sinus transverse thrombosis", "transverse sinus thrombosis", "Thrombosis, Transverse Sinus", "Sinus Thromboses, Transverse", "Thromboses, Transverse Sinus", "Thrombosis of transverse sinus", "thrombosis of lateral venous sinus", "Thrombosis of lateral venous sinus", "Thrombosis transverse sinus (disorder)", "cerebral vein thrombosis of lateral sinus", "Cerebral venous thrombosis of lateral sinus", "Thrombosis of lateral venous sinus (disorder)", "cerebral vein thrombosis of lateral sinus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lateral sinus thrombosis", "shortest_name_length": 24}
{"curie": "MONDO:0014178", "names": ["MSP2", "IBMPFD2", "multisystem proteinopathy 2", "MULTISYSTEM PROTEINOPATHY 2", "multisystem Proteinopathy 2", "HNRNPA2B1 inclusion body myopathy with Paget disease of bone and frontotemporal dementia", "INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 2", "inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2", "inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia type 2", "inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2", "inclusion body myopathy with Paget disease of bone and frontotemporal dementia caused by mutation in HNRNPA2B1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2", "shortest_name_length": 4}
{"curie": "UMLS:C1336136", "names": ["Stage IB Large Cell Lung Cancer", "Stage IB Large Cell Lung Carcinoma", "Stage IB Large Cell Carcinoma of Lung", "Stage IB Large Cell Carcinoma of the Lung", "Stage IB Lung Large Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Lung Large Cell Carcinoma AJCC v7", "shortest_name_length": 31}
{"curie": "MONDO:0006905", "names": ["PSCN", "Reed Nevus", "Spindle Cell Nevi", "Nevi, Spindle Cell", "Spindle cell nevus", "Spindle Cell Nevus", "spindle cell nevus", "Spindle cell naevus", "Nevus, Spindle Cell", "spindle cell Nevus of Reed", "Spindle cell nevus of Reed", "Spindle Cell Nevus of Reed", "Spindle cell naevus of Reed", "Pigmented Spindle Cell Nevus", "pigmented spindle cell nevus", "Spindle cell nevus (disorder)", "Pigmented spindle cell nevus of Reed", "Pigmented Spindle Cell Nevus of Reed", "Spindle cell nevus of Reed (disorder)", "Spindle cell nevus (morphologic abnormality)", "Pigmented Spindle Cell Variant of Spitz Nevus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pigmented spindle cell nevus", "shortest_name_length": 4}
{"curie": "UMLS:C2019511", "names": ["Anal Canal Squamous Papilloma", "Anal Canal Squamous Cell Papilloma", "squamous cell papilloma of anal canal", "squamous cell papilloma of anal canal (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "squamous cell papilloma of anal canal", "shortest_name_length": 29}
{"curie": "UMLS:C0085119", "names": ["FOOT ULCER", "Ulcer foot", "Foot ulcer", "Foot Ulcer", "ulcer foot", "foot ulcer", "Ulcer, Foot", "foot; ulcer", "Foot Ulcers", "foot ulcers", "ulcer; foot", "Foot--Ulcers", "Ulcers, Foot", "Ulcus cruris", "ulcer of foot", "Ulcer of foot", "of foot ulcer", "FOOT ULCERATION", "foot ulceration", "foot ulcerations", "Foot ulcerations", "Ulcer of foot, NOS", "Ulcer of foot (disorder)", "ulcer of foot (diagnosis)", "foot ulcer (physical finding)", "disorder of lower extremity foot ulcer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Foot Ulcer", "shortest_name_length": 10}
{"curie": "MONDO:0003000", "names": ["CNS Germ Cell Tumor", "CNS germ cell tumor", "CNS germ cell neoplasm", "CNS Germ Cell Neoplasm", "Germ Cell Tumor of CNS", "germ cell tumor of CNS", "Germ Cell Neoplasm of CNS", "germ cell neoplasm of CNS", "Germ Cell Tumor of the CNS", "germ cell tumor of the CNS", "germ cell tumour of the CNS", "Germ Cell Neoplasm of the CNS", "germ cell neoplasm of the CNS", "central nervous system germ cell tumor", "Central Nervous System Germ Cell Tumor", "central nervous system germ cell tumour", "Germ Cell Tumor of Central Nervous System", "central nervous system germ cell neoplasm", "Central Nervous System Germ Cell Neoplasm", "germ cell tumor of central nervous system", "central nervous system rare germ cell tumor", "Germ Cell Neoplasm of Central Nervous System", "germ cell neoplasm of central nervous system", "germ cell tumor of the central nervous system", "Germ Cell Tumor of the Central Nervous System", "germ cell neoplasm of the central nervous system", "Germ Cell Neoplasm of the Central Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system germ cell tumor", "shortest_name_length": 19}
{"curie": "MONDO:0013487", "names": ["CFDD", "FACTOR D DEFICIENCY", "Factor D Deficiency", "Factor D deficiency", "factor D deficiency", "Complement Factor D Deficiency", "COMPLEMENT FACTOR D DEFICIENCY", "Factor D deficiency (disorder)", "complement factor D deficiency", "Factor D deficiency (diagnosis)", "recurrent Neisseria infections due to factor D deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "recurrent Neisseria infections due to factor D deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0020364", "names": ["PPCD", "Schlichting dystrophy", "posterior polymorphous dystrophy", "posterior polymorphous corneal dystrophy", "corneal dystrophy, posterior polymorphous", "hereditary polymorphus posterior corneal dystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "posterior polymorphous corneal dystrophy", "shortest_name_length": 4}
{"curie": "UMLS:C5554628", "names": ["Refractory Low Grade Glioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Low Grade Glioma", "shortest_name_length": 27}
{"curie": "MONDO:0019243", "names": ["disorder of energy metabolism", "inborn disorder of energy metabolism", "inborn error of generation of precursor metabolites and energy", "inborn generation of precursor metabolites and energy disorder", "rare inborn error of generation of precursor metabolites and energy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of energy metabolism", "shortest_name_length": 29}
{"curie": "MONDO:0007362", "names": ["CRD", "CORD", "CRD2", "CORD2", "RCRD2", "CONE-ROD DYSTROPHY", "cone-rod dystrophy", "Cone Rod Dystrophy 2", "CONE-ROD DYSTROPHY 2", "cone-rod dystrophy 2", "Cone-Rod Dystrophy 2", "CRX cone-rod dystrophy", "cone-rod dystrophy type 2", "Cone-rod retinal dystrophy", "CONE-ROD RETINAL DYSTROPHY", "retinal cone-rod dystrophy", "RETINAL CONE-ROD DYSTROPHY", "cone-rod retinal dystrophy", "cone-rod retinal dystrophy-2", "retinal cone-rod dystrophy 2", "cone-rod retinal dystrophy 2", "progressive cone-rod dystrophy", "Progressive cone-rod dystrophy", "Progressive cone-rod dystrophy (disorder)", "progressive cone-rod dystrophy (diagnosis)", "cone-rod dystrophy caused by mutation in CRX"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cone-rod dystrophy 2", "shortest_name_length": 3}
{"curie": "MONDO:0019905", "names": ["r9", "Ring 9", "Ring chromosome 9", "ring chromosome 9", "Chromosome 9 Ring", "chromosome 9 ring", "Ring 9, Chromosome", "Ring chromosome type 9", "Ring chromosome 9 syndrome", "Ring chromosome 9 syndrome (disorder)", "anomaly of chromosome ring 9 syndrome", "Ring chromosome 9 syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ring chromosome 9", "shortest_name_length": 2}
{"curie": "MONDO:0010519", "names": ["ATRX", "ATRX Syndrome", "ATRX syndrome", "ATR-X syndrome", "ATR-X SYNDROME", "ATR, nondeletion type", "ATR, Nondeletion type", "ATR non deletion type", "ATR, Nondeletion Type", "ATR, NONDELETION TYPE", "XLMR-Hypotonic Face Syndrome", "XLMR hypotonic face syndrome", "Alpha Thalassemia-Mental Retardation, X-Linked", "Alpha thalassemia X-linked intellectual deficit", "Alpha thalassaemia X-linked intellectual deficit", "X-Linked Alpha-Thalassemia Mental Retardation Syndrome", "Alpha Thalassemia/Mental Retardation Syndrome X-Linked", "Alpha Thalassemia X-Linked Mental Retardation Syndrome", "X-linked alpha-thalassemia/mental retardation syndrome", "Alpha-thalassemia X-linked mental retardation syndrome", "X-linked alpha thalassemia mental retardation syndrome", "Alpha thalassemia/mental retardation syndrome X-linked", "Alpha thalassemia X-linked mental retardation syndrome", "ALPHA-thalassemia/mental retardation syndrome, X-linked", "ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED", "Alpha Thalassemia X-Linked Intellectual Disability Syndrome", "Alpha thalassemia/intellectual disability syndrome X-linked", "alpha thalassemia-X-linked intellectual disability syndrome", "Alpha-thalassemia X-linked intellectual disability syndrome", "Alpha-thalassemia-X-linked intellectual disability syndrome", "Alpha thalassemia X-linked intellectual disability syndrome", "ALPHA-thalassemia/intellectual disability syndrome, X-linked", "Alpha thalassaemia X-linked intellectual disability syndrome", "X-linked alpha-thalassemia/mental retardation syndrome (ATRX)", "alpha-thalassemia/mental retardation syndrome nondeletion type", "ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, NONDELETION TYPE", "Alpha-thalassemia/mental retardation syndrome, Nondeletion type", "alpha-thalassemia/mental retardation syndrome, nondeletion type", "Alpha-Thalassemia-Mental Retardation Syndrome, Nondeletion Type", "alpha-thalassemia/mental retardation syndrome, X-linked dominant", "alpha-thalassemia/intellectual disability syndrome nondeletion type", "Alpha-thalassemia/intellectual disability syndrome, Nondeletion type", "Alpha thalassemia X-linked intellectual disability syndrome (disorder)", "ALPHA-THALASSEMIA/IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME, X-LINKED", "Alpha-Thalassemia-Mental Retardation Syndrome, Nondeletion Type, X-Linked", "Alpha thalassemia mental retardation syndrome, nondeletion type, X-linked", "Alpha thalassemia mental retardation syndrome, non deletion type, X-linked", "Alpha thalassemia intellectual disability syndrome, nondeletion type, X-linked", "alpha-thalassemia/mental retardation syndrome, nondeletion type (ATR2, ATR, nondeletion)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alpha thalassemia-X-linked intellectual disability syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0302832", "names": ["OBSESSIVE REACTION", "Obsessive Neurosis", "Obsessive reaction", "obsessive neurosis", "Neurosis;obsessive", "neurosis; obsession", "obsession; neurosis", "obsessional neurosis", "OBSESSIONAL NEUROSIS", "Obsessional neurosis", "neurosis; obsessional", "obsessional; neurosis", "Obsessional neurosis (disorder)", "obsessional neurosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Obsessional neurosis", "shortest_name_length": 18}
{"curie": "MONDO:0004363", "names": ["adult spinal cord glioblastoma", "Adult Spinal Cord Glioblastoma", "adult Spinal Cord Glioblastoma", "Glioblastoma multiforme of spinal cord", "glioblastoma multiforme of spinal cord", "adult spinal cord glioblastoma multiforme", "Adult Spinal Cord Glioblastoma Multiforme", "Glioblastoma multiforme of spinal cord (disorder)", "glioblastoma multiforme of spinal cord (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult spinal cord glioblastoma", "shortest_name_length": 30}
{"curie": "MONDO:0004678", "names": ["ringworm", "dermatomycosis", "Dermatophytosis", "DERMATOPHYTOSES", "Dermatophycosis", "dermatophytoses", "dermatophytosis", "DERMATOPHYTOSIS", "Ringworm infection", "fungal skin disease", "Dermatophytosis NOS", "fungal skin diseases", "skin disease, fungal", "skin diseases, fungal", "Dermatophytosis (disorder)", "dermatophytosis (diagnosis)", "Dermatophytosis, unspecified", "Dermatophytosis of unspecified site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermatophytosis", "shortest_name_length": 8}
{"curie": "UMLS:C4528206", "names": ["Plasma Cell Myeloma by DS Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Plasma Cell Myeloma by DS Stage", "shortest_name_length": 31}
{"curie": "MONDO:0014548", "names": ["LQT14", "Long QT Syndrome 14", "long QT syndrome 14", "LONG QT SYNDROME 14", "CALM1 long QT syndrome", "long QT syndrome type 14", "long QT syndrome caused by mutation in CALM1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "long QT syndrome 14", "shortest_name_length": 5}
{"curie": "UMLS:C0334425", "names": ["Balloon cell nevus", "Balloon Cell Nevus", "Balloon cell naevus", "Balloon cell nevus (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Balloon cell nevus", "shortest_name_length": 18}
{"curie": "UMLS:C0852563", "names": ["Sleep Disorder due to General Medical Condition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sleep Disorder due to General Medical Condition", "shortest_name_length": 47}
{"curie": "MONDO:0011857", "names": ["ATFB3", "atrial fibrillation familial 3", "ATRIAL FIBRILLATION, FAMILIAL, 3", "Atrial Fibrillation, Familial, 3", "atrial fibrillation, familial, 3", "KCNQ1 familial atrial fibrillation", "atrial fibrillation, familial, type 3", "atrial fibrillation familial 3 (diagnosis)", "familial atrial fibrillation caused by mutation in KCNQ1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial fibrillation, familial, 3", "shortest_name_length": 5}
{"curie": "UMLS:C1265994", "names": ["Clear cell tumor", "clear cell tumor", "Clear Cell Tumor", "Clear cell tumour", "cell clear tumors", "Clear Cell Neoplasm", "Clear cell tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clear cell tumor", "shortest_name_length": 16}
{"curie": "MONDO:0002562", "names": ["demyelinating disease", "demyelinated diseases", "Demyelinating Disease", "disease demyelinating", "Demyelinating Disorder", "demyelinating diseases", "demyelinating disorder", "Demyelinating Diseases", "demyelination disorders", "demyelinating disorders", "Demyelinating Disorders", "Demyelinating disorders", "Demyelination disorder NOS", "Demyelinating nervous system disease or syndrome", "Demyelinating Nervous System Diseases and Syndromes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "demyelinating disease", "shortest_name_length": 21}
{"curie": "UMLS:C0423690", "names": ["facet syndrome", "facet joint pain", "Facet joint pain", "facet joint syndrome", "Facet joint syndrome", "facet syndrome (diagnosis)", "Facet joint pain (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Facet joint pain", "shortest_name_length": 14}
{"curie": "UMLS:C4525136", "names": ["Stage IIB Rectal Cancer", "Stage IIB Rectal Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Rectal Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "UMLS:C1608945", "names": ["Exfoliative rash"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Exfoliative rash", "shortest_name_length": 16}
{"curie": "UMLS:C1959588", "names": ["Angioma", "angioma", "ANGIOMA", "angiomas", "Angiomas", "Angioma (benign)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Angioma", "shortest_name_length": 7}
{"curie": "MONDO:0030035", "names": ["LEUDEN", "LEUDEN SYNDROME", "Leuden Syndrome", "LEUKOENCEPHALOPATHY, DEVELOPMENTAL DELAY, AND EPISODIC NEUROLOGIC REGRESSION SYNDROME", "leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C0004601", "names": ["BACK INJURY", "Back injury", "Back Injury", "back injury", "Injury;back", "injury; back", "back; injury", "Injury, Back", "Back Injuries", "back injuries", "Injury of back", "Injuries, Back", "Back injury NOS", "back injury (diagnosis)", "Traumatic or non-traumatic injury of back", "Traumatic or non-traumatic injury of back (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Back Injuries", "shortest_name_length": 11}
{"curie": "MONDO:0019148", "names": ["Wolman", "Wolman Disease", "wolman disease", "WOLMAN DISEASE", "LAL DEFICIENCY", "Wolman disease", "LIPA DEFICIENCY", "LIPA deficiency", "Disease, Wolman", "wolmans disease", "Wolmans Disease", "Wolman's disease", "wolman's disease", "Wolman's Disease", "Disease, Wolman's", "Wolman xanthomatosis", "Xanthomatosis, Wolman", "Xanthomatosis, Wolmans", "Familial Xanthomatosis", "Wolman's Xanthomatosis", "Acid lipase deficiency", "acid lipase deficiency", "familial xanthomatosis", "Acid Lipase Deficiency", "Familial Xanthomatoses", "Xanthomatosis, Wolman's", "Xanthomatosis, Familial", "Xanthomatosis, familial", "Xanthomatoses, Familial", "xanthomatosis, familial", "acid esterase deficiency", "Acid esterase deficiency", "Wolman disease (diagnosis)", "Wolman's disease (disorder)", "primary familial xanthomatosis", "Primary familial xanthomatosis", "Familial visceral xanthomatosis", "familial visceral xanthomatosis", "Lysosomal acid lipase deficiency", "Lysosomal Acid Lipase Deficiency", "lysosomal acid lipase deficiency", "LYSOSOMAL ACID LIPASE DEFICIENCY", "CHOLESTEROL ESTER HYDROLASE DEFICIENCY", "liposomal acid lipase deficiency, Wolman type", "Liposomal Acid Lipase Deficiency, Wolman Type", "Familial xanthomatosis with adrenal involvement", "Wolman's or triglyceride storage type III disease", "Wolman's or triglyceride storage Type III disease", "Acid Cholesteryl Ester Hydrolase Deficiency, Wolman Type", "primary familial xanthomatosis with adrenal calcification", "Primary familial xanthomatosis with adrenal calcification", "Wolman Disease with Hypolipoproteinemia and Acanthocytosis", "Wolman disease with hypolipoproteinemia and acanthocytosis", "deficiency of cholesterol esterase and triacylglycerol lipase", "Deficiency of cholesterol esterase and triacylglycerol lipase", "Deficiency of cholesterol esterase AND triacylglycerol lipase"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wolman disease", "shortest_name_length": 6}
{"curie": "MONDO:0019428", "names": ["fried syndrome", "Fried syndrome", "Fried syndrome (disorder)", "Fried syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fried syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0024468", "names": ["Anterior", "adenohypophysis disease", "Adenohypophyseal Disease", "Disease, Adenohypophyseal", "Adenohypophyseal Diseases", "disease of adenohypophysis", "Anterior Pituitary Disease", "anterior pituitary disease", "Diseases, Adenohypophyseal", "Anterior pituitary disease", "Pituitary Disease, Anterior", "Disease, Anterior Pituitary", "disorder of adenohypophysis", "Anterior Pituitary Diseases", "Disorder of adenohypophysis", "Diseases, Anterior Pituitary", "Pituitary Diseases, Anterior", "Disease of anterior pituitary", "disorder of anterior pituitary", "Diseases of Anterior Pituitary", "Disorder of anterior pituitary", "anterior pituitary gland disorder", "Disease of anterior pituitary, NOS", "adenohypophysis disease or disorder", "Disorder of anterior pituitary, NOS", "disorder of anterior pituitary gland", "disease or disorder of adenohypophysis", "DISEASES OF THE ANTERIOR PITUITARY GLAND", "Disorder of anterior pituitary (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anterior pituitary gland disorder", "shortest_name_length": 8}
{"curie": "MONDO:0002426", "names": ["lung sarcoma", "Lung Sarcoma", "sarcoma lung", "lung sarcomas", "lungs sarcoma", "sarcoma of lung", "Sarcoma of lung", "Sarcoma of Lung", "Pulmonary Sarcoma", "Pulmonary sarcoma", "pulmonary sarcoma", "sarcoma of the lung", "Sarcoma of the Lung", "Sarcoma of lung (disorder)", "sarcoma of lung (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung sarcoma", "shortest_name_length": 12}
{"curie": "MONDO:0002404", "names": ["Liver Angioma", "liver angioma", "Hepatic Angioma", "hepatic angioma", "Hepatic angioma", "Angioma of Liver", "hemangioma liver", "LIVER, CAVERNOMA", "liver hemangioma", "Liver Hemangioma", "angiomas hepatic", "angioma of liver", "Liver hemangioma", "LIVER HEMANGIOMA", "hemangiomas liver", "Liver hemangiomas", "LIVER, HEMANGIOMA", "liver haemangioma", "haemangioma liver", "Hepatic Hemangioma", "Hepatic hemangioma", "hepatic hemangioma", "HEPATIC HEMANGIOMA", "hemangioma hepatic", "hemangioma of liver", "Hemangioma of Liver", "hepatic haemangioma", "Hemangioma of liver", "Hepatic haemangioma", "hemangiomas hepatic", "Haemangioma of liver", "angioma of the liver", "Angioma of the Liver", "Hemangioma of the liver", "hemangioma of the liver", "Hemangioma of the Liver", "cavernous hemangioma liver", "liver cavernous hemangioma", "benign hemangioma of liver", "cavernous hemangiomas liver", "LIVER, HEMANGIOMA, CAVERNOUS", "Hemangioma of liver (disorder)", "benign hemangioma of liver (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "liver hemangioma", "shortest_name_length": 13}
{"curie": "MONDO:0017282", "names": ["echinococcosis", "Alveolococcosis", "alveolococcosis", "Alveolar hydatid", "small fox tapeworm", "multilocular hydatid", "Multilocular hydatid", "Alveolar echinococcosis", "alveolar echinococcosis", "Alveolar hydatid disease", "Multilocular echinococcosis", "echinococcus multilocularis", "multilocularis; Echinococcus", "Echinococcus; multilocularis", "Echinococcus multilocularis infection", "Echinococcus Multilocularis Infection", "echinococcus multilocularis infection", "echinococcus multilocularis (diagnosis)", "Echinococcus multilocularis infectious disease", "Echinococcus multilocularis disease or disorder", "Echinococcus multilocularis infection (disorder)", "Tapeworm infection by Echinococcus multilocularis", "Echinococcus multilocularis infection, unspecified", "Echinococcus multilocularis caused disease or disorder", "Echinococcus multilocularis infection, other and multiple sites"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alveolar echinococcosis", "shortest_name_length": 14}
{"curie": "MONDO:0014595", "names": ["DEE30", "EIEE30", "early infantile epileptic encephalopathy 30", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 30", "developmental and epileptic encephalopathy 30", "epileptic encephalopathy, early infantile, 30", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 30", "SIK1 early infantile epileptic encephalopathy", "developmental and epileptic encephalopathy, 30", "epileptic encephalopathy, early infantile, type 30", "early infantile epileptic encephalopathy caused by mutation in SIK1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 30", "shortest_name_length": 5}
{"curie": "MONDO:0000425", "names": ["X-linked disease", "disease, X-linked", "X-linked genetic disease", "X-Linked Genetic Disease", "X-linked genetic diseases", "Disease, X-Linked Genetic", "X-Linked Genetic Diseases", "disease, X-linked genetic", "X Linked Genetic Diseases", "X linked genetic diseases", "Genetic Disease, X-Linked", "genetic disease, X-linked", "diseases, X-linked genetic", "X-linked inherited disease", "Diseases, X-Linked Genetic", "Genetic Diseases, X Linked", "Genetic Diseases, X-Linked", "genetic diseases, X linked", "X-linked monogenic disease", "X-linked inherited disorder", "X-linked hereditary disease", "X-Linked Inherited Disorder", "X-linked hereditary disorder", "X-linked disease or disorder", "disease or disorder, X-linked", "Genetic Diseases, X-Chromosome Linked", "genetic diseases, X-chromosome linked", "Genetic Diseases, X Chromosome Linked", "genetic diseases, X chromosome linked", "sex-linked hereditary disease X-linked", "X-linked hereditary disease (disorder)", "X-linked hereditary disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked disease", "shortest_name_length": 16}
{"curie": "UMLS:C5669739", "names": ["Granular Cell Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Granular Cell Astrocytoma", "shortest_name_length": 25}
{"curie": "MONDO:0006879", "names": ["papillitis", "Choked disk", "disk, Choked", "Choked disks", "retinal edema", "disks, Choked", "retinal Edemas", "edema, retinal", "optic discitis", "Edemas, retinal", "optic papillitis", "optic disk edema", "edema, optic disk", "papillitis, optic", "Edemas, optic disk", "optic papilla edema", "edema, optic papilla", "optic nerve papillitis", "papillitis, optic nerve", "optic disc inflammation", "edema of the optic disc", "inflammation of optic disc", "Papilledema due to raised intracranial pressure", "Papilloedema due to raised intracranial pressure", "Decreased Intraocular Pressure-Associated Papilledema", "decreased intraocular pressure associated papilledema", "decreased intraocular pressure-associated papilledema", "Decreased Intraocular Pressure Associated Papilledema", "increased intracranial pressure-associated papilledema", "Increased Intracranial Pressure-Associated Papilledema", "Increased Intracranial Pressure Associated Papilledema", "increased intracranial pressure associated papilledema", "Papilledema Associated with Decreased Intraocular Pressure", "papilledema associated with decreased intraocular pressure", "Papilledema associated with increased intracranial pressure", "papilledema associated with increased intracranial pressure", "Papilledema Associated with Increased Intracranial Pressure", "Papilledema - optic disc edema due to raised intracranial pressure", "Papilloedema - optic disc oedema due to raised intracranial pressure", "papilledema associated with increased intracranial pressure (diagnosis)", "Papilledema - optic disc edema due to raised intracranial pressure (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "optic papillitis", "shortest_name_length": 10}
{"curie": "UMLS:C5419028", "names": ["Recurrent Extrarenal Rhabdoid Tumor of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Extrarenal Rhabdoid Tumor of the Ovary", "shortest_name_length": 48}
{"curie": "MONDO:0002548", "names": ["CSCHW", "cellular neurinoma", "Cellular Neurinoma", "cellular Neurinoma", "cellular schwannoma", "Cellular Schwannoma", "Cellular schwannoma", "Cellular Neurilemmoma", "cellular neurilemmoma", "Cellular neurilemmoma", "Cellular schwannoma (disorder)", "Cellular schwannoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cellular schwannoma", "shortest_name_length": 5}
{"curie": "MONDO:0011001", "names": ["BRGDA1", "Brugada Syndrome 1", "BRUGADA SYNDROME 1", "Brugada syndrome 1", "SCN5A Brugada syndrome", "Brugada syndrome type 1", "Brugada syndrome 1 (diagnosis)", "Cardiac conduction defect, nonspecific", "sudden unexplained nocturnal death syndrome", "Brugada syndrome caused by mutation in SCN5A", "right bundle branch block, St segment elevation, and sudden death syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brugada syndrome 1", "shortest_name_length": 6}
{"curie": "UMLS:C4764229", "names": ["Recurrent Spindle Cell Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Spindle Cell Sarcoma", "shortest_name_length": 30}
{"curie": "UMLS:C4086171", "names": ["Small Intestinal Cancer", "Childhood Small Intestinal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Small Intestinal Carcinoma", "shortest_name_length": 23}
{"curie": "UMLS:C1297882", "names": ["Partial Trisomy", "partial trisomy", "Partial trisomy", "partial; trisomy", "trisomy; partial", "Trisomy, Partial", "Partial Trisomies", "Trisomies, Partial", "partial trisomy (diagnosis)", "Partial trisomy (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Partial Trisomy", "shortest_name_length": 15}
{"curie": "MONDO:0010168", "names": ["US1", "USH1", "USH1A", "Usher Syndrome Type 1", "Usher syndrome type 1", "Usher syndrome, type 1", "USHER syndrome, type I", "Usher syndrome, type 1A", "Usher syndrome, type 1B", "Usher syndrome, type Ia", "Usher syndrome, type Ia, formerly", "Usher syndrome, type I, French variety", "retinitis pigmentosa and congenital deafness", "Usher syndrome, type I, French variety, formerly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Usher syndrome type 1", "shortest_name_length": 3}
{"curie": "UMLS:C5446444", "names": ["Lacrimal Drainage System Inverted Papilloma", "Inverted Papilloma of the Lacrimal Drainage System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lacrimal Drainage System Inverted Papilloma", "shortest_name_length": 43}
{"curie": "UMLS:C4054162", "names": ["Posterior Urethral Valves Type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Posterior Urethral Valves Type 3", "shortest_name_length": 32}
{"curie": "MONDO:0022802", "names": ["Collins-Sakati syndrome", "Collins Sakati syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Collins-Sakati syndrome", "shortest_name_length": 23}
{"curie": "UMLS:C5556434", "names": ["NSMP Endometrial Endometrioid Carcinoma", "NSMP Endometrial Endometrioid Adenocarcinoma", "No Specific Molecular Profile Endometrial Endometrioid Carcinoma", "No Specific Molecular Profile Endometrial Endometrioid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "No Specific Molecular Profile Endometrial Endometrioid Adenocarcinoma", "shortest_name_length": 39}
{"curie": "UMLS:C3897509", "names": ["Stage IVC Sinonasal Squamous Cell Carcinoma AJCC v7", "Stage IVC Nasal Cavity and Paranasal Sinus Squamous Cell Cancer", "Stage IVC Nasal Cavity and Paranasal Sinus Squamous Cell Carcinoma", "Stage IVC Nasal Cavity and Paranasal Sinus Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Sinonasal Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 51}
{"curie": "MONDO:0018801", "names": ["CAVD", "CBAVD", "Absent Vasa", "Absence of Vas Deferens", "Congenital Aplasia of Vas Deferens", "Congenital Absence of Vas Deferens", "Congenital bilateral aplasia of vas deferens", "congenital bilateral aplasia of vas deferens", "Congenital bilateral absence of vas deferens", "Congenital Bilateral Absence of Vas Deferens", "congenital bilateral absence of vas deferens", "VAS DEFERENS, CONGENITAL BILATERAL APLASIA OF", "Vas Deferens, Congenital Bilateral Aplasia Of", "Congenital bilateral agenesis of vas deferens", "congenital bilateral agenesis of vas deferens", "Congenital bilateral absence of the vas deferens", "Congenital Bilateral Aplasia of the Vas Deferens", "Congenital bilateral aplasia of vas deferens (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital bilateral absence of vas deferens", "shortest_name_length": 4}
{"curie": "MONDO:0004699", "names": ["gastrointestinal lymphoma", "GASTROINTESTINAL LYMPHOMA", "lymphoma gastrointestinal", "Digestive System Lymphoma", "digestive system lymphoma", "Gastrointestinal Lymphoma", "Gastrointestinal lymphoma", "lymphoma of digestive system", "primary gastrointestinal lymphoma", "Primary Digestive System Lymphoma", "primary digestive system lymphoma", "Primary Gastrointestinal Lymphoma", "Lymphoma of gastrointestinal tract", "Lymphoma of gastrointestinal tract (disorder)", "Lymphoma of gastrointestinal tract (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastrointestinal lymphoma", "shortest_name_length": 25}
{"curie": "UMLS:C0854453", "names": ["Escherichia sepsis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Escherichia sepsis", "shortest_name_length": 18}
{"curie": "MONDO:0100493", "names": ["autosomal recessive titinopathy", "TTN-related myopathy, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive titinopathy", "shortest_name_length": 31}
{"curie": "MONDO:0014859", "names": ["DEE37", "EIEE37", "early infantile epileptic encephalopathy 37", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 37", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 37", "epileptic encephalopathy, early infantile, 37", "developmental and epileptic encephalopathy 37", "developmental and epileptic encephalopathy, 37", "FRRS1L early infantile epileptic encephalopathy", "epileptic encephalopathy, early infantile, type 37", "epileptic encephalopathy, early infantile, 37; EIEE37", "early infantile epileptic encephalopathy caused by mutation in FRRS1L"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 37", "shortest_name_length": 5}
{"curie": "UMLS:C0278484", "names": ["dukes d colon cancer", "Dukes D colon cancer", "Colon cancer Dukes D", "colon cancer stage iv", "cancer colon iv stage", "colon cancer, Dukes D", "stage IV colon cancer", "duke's d colon cancer", "Colon cancer stage IV", "colon cancer, stage IV", "Colon cancer metastatic", "cancer colon metastatic", "metastatic colon cancer", "Metastatic colon cancer", "colon cancer metastatic", "colon cancer, metastatic", "Astler-Coller D colon cancer", "colon cancer, Astler-Coller D", "Malignant neoplasm of colon stage IV", "Malignant neoplasm of colon stage IV, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant neoplasm of colon stage IV", "shortest_name_length": 20}
{"curie": "MONDO:0012600", "names": ["AUTS9", "AUTISM, SUSCEPTIBILITY TO, 9", "autism, susceptibility to, 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autism, susceptibility to, 9", "shortest_name_length": 5}
{"curie": "UMLS:C4727148", "names": ["Recurrent Aplastic Anemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Aplastic Anemia", "shortest_name_length": 25}
{"curie": "UMLS:C4553245", "names": ["II", "Stage II Thyroid Gland Papillary Cancer", "Stage II Thyroid Gland Papillary Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Thyroid Gland Papillary Carcinoma AJCC v8", "shortest_name_length": 2}
{"curie": "UMLS:C0280378", "names": ["nasopharynx squamous cell carcinoma, stage I", "Nasopharyngeal squamous cell carcinoma stage I", "nasopharyngeal squamous cell carcinoma, stage I", "epidermoid carcinoma of the nasopharynx, stage I", "stage I squamous cell carcinoma of the nasopharynx", "squamous cell carcinoma of the nasopharynx, stage I", "Stage I Nasopharyngeal Keratinizing Epidermoid Carcinoma", "Stage I Keratinizing Epidermoid Carcinoma of Nasopharynx", "Stage I Keratinizing Squamous Cell Carcinoma of Nasopharynx", "Stage I Nasopharyngeal Keratinizing Squamous Cell Carcinoma", "Stage I Keratinizing Epidermoid Carcinoma of the Nasopharynx", "Stage I Keratinizing Squamous Cell Carcinoma of the Nasopharynx", "Stage I Nasopharyngeal Throat Keratinizing Squamous Cell Cancer", "Stage I Nasopharyngeal Keratinizing Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasopharyngeal squamous cell carcinoma stage I", "shortest_name_length": 44}
{"curie": "MONDO:0008603", "names": ["TRIGNO1", "TRIGONOCEPHALY 1", "trigonocephaly 1", "Metopic Synostoses", "Metopic synostosis", "Metopic Synostosis", "Synostoses, Metopic", "Synostosis, Metopic", "trigonocephaly type 1", "Metopic craniosynostosis", "Craniosynostosis, Metopic", "craniosynostosis, metopic", "CRANIOSYNOSTOSIS, METOPIC", "Trigonocephaly, Nonsyndromic", "FGFR1 isolated trigonocephaly", "Metopic suture craniosynostosis", "Craniosynostosis (metopic suture)", "Interfrontal craniofaciosynostosis", "Interfrontal craniofaciosynostosis (disorder)", "isolated trigonocephaly caused by mutation in FGFR1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trigonocephaly 1", "shortest_name_length": 7}
{"curie": "MONDO:0014320", "names": ["BBSOAS", "BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME", "Bosch-Boonstra-Schaaf optic atrophy syndrome", "Bosch Boonstra Schaaf optic atrophy syndrome", "optic atrophy-intellectual disability syndrome", "Optic atrophy-intellectual disability syndrome", "Optic atrophy, intellectual disability syndrome", "optic atrophy, intellectual disability syndrome", "BBSOAS - Bosch Boonstra Schaaf optic atrophy syndrome", "Optic atrophy, intellectual disability syndrome (disorder)", "optic atrophy, intellectual disability syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bosch-Boonstra-Schaaf optic atrophy syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0007042", "names": ["SCS", "ACS3", "ACS 3", "ACS III", "BPES3, FORMERLY", "CHOTZEN SYNDROME", "Chotzen syndrome", "Chotzen Syndrome", "chotzen syndrome", "Syndrome, Chotzen", "saethre chotzen syndrome", "saethre-chotzen syndrome", "Saethre-Chotzen Syndrome", "Saethre-Chotzen syndrome", "Saethre Chotzen syndrome", "SAETHRE-CHOTZEN SYNDROME", "Saethre Chotzen Syndrome", "Acrocephalosyndactyly III", "acrocephalosyndactyly III", "Syndrome, Saethre-Chotzen", "Acrocephalosyndactyly IIIs", "acrocephalosyndactyly type 3", "Acrocephalosyndactyly type 3", "acrocephalosyndactyly, type 3", "Acrocephalosyndactyly, Type 3", "type III Acrocephalosyndactyly", "Type III Acrocephalosyndactyly", "Saethre-Chotzen syndrome (SCS)", "acrocephalosyndactyly type III", "acrocephalo-syndactyly, type 3", "Acrocephalosyndactyly Type III", "Acrocephalosyndactylies, Type 3", "ACROCEPHALOSYNDACTYLY, TYPE III", "Acrocephalosyndactyly, type III", "Acrocephalosyndactyly, Type III", "Acrocephalosyndactylies, Type III", "Saethre-Chotzen syndrome (disorder)", "acrocephalosyndactyly III (ACS III)", "Acrocephalosyndactyly syndrome, type III", "Dysostosis Craniofacialis with Hypertelorism", "dysostosis craniofacialis with hypertelorism", "Saethre-Chotzen Syndrome with Eyelid Anomalies", "SAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES", "Saethre-Chotzen syndrome with eyelid anomalies", "Acrocephaly, Skull Asymmetry, and Mild Syndactyly", "ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLY", "acrocephaly, skull asymmetry, and mild syndactyly", "blepharophimosis, epicanthus inversus, and ptosis 3", "Saethre-Chotzen syndrome with or without eyelid anomalies", "BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY", "blepharophimosis, epicanthus inversus, and ptosis 3, formerly", "blepharophimosis,epicanthus inversus, and ptosis 3 (formerly)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Saethre-Chotzen syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0005381", "names": ["osteopathy", "OSTEOPATHY", "Osteopathy", "Osteopathia", "Bone disease", "Bone Disease", "Disease;bone", "bone disease", "Disease, Bone", "Bone disorder", "BONE DISORDER", "bone diseases", "bone disorder", "bones disease", "Bone Diseases", "bones diseases", "bone; disorder", "Bone Disorders", "Diseases, Bone", "bone disorders", "disease of bone", "Bones--Diseases", "bones disorders", "Disease of bone", "skeletal disease", "Disorder of bone", "Osteopathia, NOS", "Bone disease, NOS", "Diseases of Bones", "Bone disorder NOS", "Bone disorder (NOS)", "DISORDER BONE (NOS)", "Disorder bone (NOS)", "BONE DISORDER (NOS)", "bone element disease", "Disease of bone, NOS", "DISEASES OF THE BONES", "diseases of the bones", "the diseases of bones", "disease of bone element", "disorder of bone element", "bone disorder (diagnosis)", "disease (or disorder); bone", "Disorder of bone (disorder)", "Unspecified disorder of bone", "Disorder of bone, unspecified", "bone element disease or disorder", "disease or disorder of bone element", "rare bone disease related to a common gene or pathway defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bone disorder", "shortest_name_length": 10}
{"curie": "UMLS:C0855215", "names": ["Testicular yolk sac tumor stage III", "Stage III Testicular Yolk Sac Tumor", "Testicular yolk sac tumour stage III", "Testicular endodermal sinus tumor stage III", "Stage III Testicular Yolk Sac Tumor AJCC v7", "Stage III Testicular Yolk Sac Tumor AJCC v6", "Testicular endodermal sinus tumour stage III", "Stage III Testicular Yolk Sac Tumor AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular yolk sac tumor stage III", "shortest_name_length": 35}
{"curie": "UMLS:C2698203", "names": ["Metastatic Breast Ductal Carcinoma", "Metastatic Ductal Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Breast Ductal Carcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0010469", "names": ["AUTSX6", "TMLHED", "susceptibility to X-linked autism 6", "autism, susceptibility to, X-linked 6", "AUTISM, SUSCEPTIBILITY TO, X-LINKED 6", "EPSILON-TRIMETHYLLYSINE HYDROXYLASE DEFICIENCY", "epsilon-trimethyllysine hydroxylase deficiency", "EPSILON-trimethyllysine HYDROXYLASE deficiency", "autism, susceptibility to, X-linked 6, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epsilon-trimethyllysine hydroxylase deficiency", "shortest_name_length": 6}
{"curie": "MONDO:0100055", "names": ["intraosseous rhabdomyosarcoma with FUS-TFCP2 fusion", "intraosseous rhabdomyosarcoma defined by FUS-TFCP2 fusion", "Intraosseous Spindle Cell Rhabdomyosarcoma with TFCP2/NCOA2 Rearrangements", "intraosseous spindle cell rhabdomyosarcoma with TFCP2/NCOA2 rearrangements"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intraosseous spindle cell rhabdomyosarcoma with TFCP2/NCOA2 rearrangements", "shortest_name_length": 51}
{"curie": "UMLS:C4520915", "names": ["Stage IA Soft Tissue Sarcoma", "Stage IA Adult Sarcoma of Soft Tissue", "Stage IA Adult Sarcoma of the Soft Tissue", "Stage IA Adult Soft Tissue Sarcoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Adult Soft Tissue Sarcoma AJCC v7", "shortest_name_length": 28}
{"curie": "MONDO:0002182", "names": ["Speech therapy", "disorder communication", "communicative disorder", "Communication disorder", "Impaired Communication", "Communicative Disorder", "communication disorder", "Communication Disorder", "Communicative disorders", "disorders communication", "Communicative Disorders", "communication disorders", "Communication Disorders", "Communication disorders", "communicative disorders", "communications disorders", "Communication impairment", "communication impairment", "COMMUNICATION IMPAIRMENT", "Communications disorders", "Communication Impairment", "Communication disorder NOS", "Communication disorder, NOS", "RNDx communication impairment", "communication disorder diagnosis", "Communication disorder (disorder)", "communication disorder (diagnosis)", "Communication disorders and disturbances", "RNDx communication impairment (diagnosis)", "communication impairment (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "communication disorder", "shortest_name_length": 14}
{"curie": "MONDO:0043959", "names": ["lymphocytoma", "Lymphocytoma", "lymphocytomas", "Lymphocytomas", "PSEUDOLYMPHOMA", "Pseudolymphoma", "pseudolymphoma", "pseudolymphomas", "pseudo lymphoma", "Pseudo lymphoma", "PSEUDO LYMPHOMA", "Pseudolymphomas", "Pseudolymphoma, NOS", "Lymphoid Hyperplasia", "Lymphoid hyperplasia", "lymphoid hyperplasia", "hyperplasia lymphoid", "LYMPHOID HYPERPLASIA", "Lymphoid Hyperplasias", "LYMPHOID HYPERPLASIAS", "Hyperplasia, lymphoid", "LYMPHOMA LIKE REACTION", "LYMPHOMA-LIKE DISORDER", "Lymphoma-like reaction", "REACTION LYMPHOMA-LIKE", "Lymphoma like reaction", "Reaction lymphoma-like", "LYMPHOMA-LIKE REACTION", "Lymphoma-like disorder", "Lymphoid hyperplasia, NOS", "Pseudolymphoma (disorder)", "pseudolymphoma (diagnosis)", "Benign lymphoid hyperplasia", "benign lymphoid hyperplasia", "Benign Lymphoid Hyperplasia", "nodular lymphoid hyperplasia", "Nodular lymphoid hyperplasia", "hyperplasia lymphoid nodular", "Lymphoid nodular hyperplasia", "lymphoid nodular hyperplasia", "reactive lymphoid hyperplasia", "Reactive lymphoid hyperplasia", "Reactive Lymphoid Hyperplasia", "hyperplasia lymphoid reactive", "hyperplasia, reactive lymphoid", "Lymphoid Hyperplasia, Reactive", "lymphoid hyperplasia, reactive", "Reactive Lymphoid Hyperplasias", "reactive lymphoid Hyperplasias", "Hyperplasia, Reactive Lymphoid", "hyperplasias, reactive lymphoid", "Hyperplasias, Reactive Lymphoid", "Lymphoid Hyperplasias, Reactive", "lymphoid Hyperplasias, reactive", "Lymphoid hyperplasia (disorder)", "Lymphonodular hyperplasia of the colon", "Lymphoid hyperplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudolymphoma", "shortest_name_length": 12}
{"curie": "MONDO:0010251", "names": ["MRX50", "XLID50", "X-linked mental retardation 50", "mental retardation, X-linked 50", "MENTAL RETARDATION, X-LINKED 50", "Mental Retardation, X-Linked 50", "intellectual disability, X-linked 50", "X-linked intellectual developmental disorder 50", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 50", "intellectual developmental disorder, X-linked 50", "non-syndromic X-linked intellectual disability 50"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 50", "shortest_name_length": 5}
{"curie": "MONDO:0004187", "names": ["Nodular fasciitis", "nodular fasciitis", "Nodular Fasciitis", "fasciitis nodular", "fasciitis; nodular", "nodular; fasciitis", "FASCIITIS, NODULAR", "fasciitis - nodular", "Fasciitis - nodular", "Infiltrative fasciitis", "pseudosarcomatous fasciitis", "Pseudosarcomatous fasciitis", "Pseudosarcomatous Fasciitis", "Nodular fasciitis (disorder)", "nodular fasciitis (diagnosis)", "Pseudosarcomatous fibromatosis", "Pseudosarcomatous Fibromatosis", "pseudosarcomatous fibromatosis", "fibromatosis; pseudosarcomatous", "pseudosarcomatous; fibromatosis", "Nodular fasciitis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nodular fasciitis", "shortest_name_length": 17}
{"curie": "UMLS:C0678053", "names": ["Stage IV Adrenal Cortex Cancer", "stage IV adrenocortical cancer", "Stage IV Adrenocortical Carcinoma", "Stage IV Adrenal Cortex Carcinoma", "Stage IV Carcinoma of Adrenal Cortex", "Stage IV Carcinoma of the Adrenal Cortex", "Stage IV Adrenal Cortex Carcinoma AJCC v7", "Stage IV Adrenal Cortical Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Adrenal Cortex Carcinoma AJCC v7", "shortest_name_length": 30}
{"curie": "MONDO:0002732", "names": ["tumor lung benign", "Benign Lung Tumor", "lung tumor benign", "tumor of the lung", "benign lung tumor", "benign lung tumors", "Benign lung neoplasm", "Benign tumor of lung", "benign tumor of lung", "Neoplasm benign;lung", "benign lung neoplasm", "Benign Tumor of Lung", "Benign Lung Neoplasm", "lung benign neoplasm", "Benign tumour of lung", "benign neoplasm of lung", "Benign Neoplasm of Lung", "Benign neoplasm of lung", "benign tumor of the lung", "Benign Tumor of the Lung", "benign neoplasm of the lung", "Benign Neoplasm of the Lung", "Benign neoplasm of lung, NOS", "Benign neoplasm of lung (disorder)", "benign neoplasm of lung (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung benign neoplasm", "shortest_name_length": 17}
{"curie": "UMLS:C5428721", "names": ["Lacrimal System Carcinoma", "Lacrimal Apparatus Carcinoma", "carcinoma of lacrimal apparatus", "carcinoma of lacrimal apparatus (diagnosis)", "eye neoplasm malignant lacrimal apparatus carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma of lacrimal apparatus", "shortest_name_length": 25}
{"curie": "MONDO:0015282", "names": ["Krasnow Qazi syndrome", "Krasnow-Qazi syndrome", "Krasnow Qazi Yermakov syndrome", "cardiomyopathy cataract hip spine disease", "cardiomyopathy-cataract-hip spine disease syndrome", "Cardiomyopathy-cataract-hip spine disease syndrome", "Cardiomyopathy with cataract and hip spine disease syndrome", "Cardiomyopathy with cataract and hip spine disease syndrome (disorder)", "familial dilated cardiomyopathy associated with cataracts and hip-spine disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiomyopathy-cataract-hip spine disease syndrome", "shortest_name_length": 21}
{"curie": "UMLS:C2348875", "names": ["BilIN-3", "High-Grade BilIN", "High Grade BilIN", "Biliary Intraepithelial Neoplasia-3", "Grade 3 Biliary Intraepithelial Neoplasia", "Biliary intraepithelial neoplasia, grade 3", "High-Grade Biliary Intraepithelial Neoplasia", "High Grade Biliary Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High-Grade Biliary Intraepithelial Neoplasia", "shortest_name_length": 7}
{"curie": "MONDO:0005486", "names": ["Hypodontia", "hypodontia", "oligodontia", "Oligodontia", "tooth agenesis", "Partial anodontia", "familial tooth agenesis", "selective tooth agenesis", "Partial absence of teeth", "tooth agenesis, selective", "Missing between one and six teeth", "partial congenital absence of teeth", "Congenital partial absence of teeth", "Partial congenital absence of teeth", "Congenital absence of few teeth (disorder)", "Partial congenital absence of teeth (disorder)", "partial congenital absence of teeth (diagnosis)", "Failure of development of between one and six teeth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tooth agenesis", "shortest_name_length": 10}
{"curie": "UMLS:C1265933", "names": ["Diffuse Hyperplasia", "Diffuse hyperplasia", "Diffuse hyperplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse hyperplasia", "shortest_name_length": 19}
{"curie": "MONDO:0017468", "names": ["congenital shoulder dislocation", "shoulder; dislocation, congenital", "dislocation; shoulder, congenital", "Congenital dislocation of shoulder", "True congenital shoulder dislocation", "congenital dislocation of shoulder region", "Congenital dislocation of shoulder (disorder)", "congenital dislocation of shoulder region (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital shoulder dislocation", "shortest_name_length": 31}
{"curie": "UMLS:C0409962", "names": ["Localized osteoarthrosis", "Localised osteoarthrosis", "localized osteoarthritis", "Localised osteoarthritis", "Localized osteoarthritis", "Osteoarthritis; localized", "osteoarthrosis; localized", "localized; osteoarthrosis", "Localised osteoarthropathy", "Localized osteoarthropathy", "Localized osteoarthritis, NOS", "Localized osteoarthrosis, NOS", "Localized osteoarthropathy, NOS", "Localized osteoarthrosis (disorder)", "localized osteoarthritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized osteoarthrosis", "shortest_name_length": 24}
{"curie": "MONDO:0010023", "names": ["STCD", "IMD48", "SCID, atypical", "ZAP70 deficiency", "ZAP 70 deficiency", "ZAP-70 deficiency", "Zap70-Related Scid", "IMMUNODEFICIENCY 48", "immunodeficiency 48", "Immunodeficiency 48", "SELECTIVE T-CELL DEFECT", "Selective T-Cell Defect", "selective T-cell defect", "Zeta-Associated Protein 70 Deficiency", "Zeta-associated-protein 70 deficiency", "zeta-associated-protein 70 deficiency", "Severe combined immunodeficiency, atypical", "Zap70-Related Severe Combined Immunodeficiency", "Combined immunodeficiency due to ZAP70 deficiency", "combined immunodeficiency due to ZAP70 deficiency", "severe combined immunodeficiency due to ZAP70 deficiency", "immunodeficiency disorders combined due to ZAP70 deficiency", "Combined immunodeficiency due to Zeta-chain associated protein kinase 70 deficiency", "Combined immunodeficiency due to ZAP70 (Zeta-chain associated protein kinase 70) deficiency", "Combined immunodeficiency due to Zeta-chain associated protein kinase 70 deficiency (disorder)", "Combined immunodeficiency due to Zeta-chain associated protein kinase 70 deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined immunodeficiency due to ZAP70 deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0022799", "names": ["URTICARIA COLD", "COLD URTICARIA", "Cold urticaria", "Urticaria cold", "urticaria cold", "cold urticaria", "Urticaria due to cold", "cold contact urticaria", "Cold-induced urticaria", "cold-induced urticaria", "cold induced urticaria", "Urticaria, cold-induced", "Urticaria caused by cold", "urticaria idiopathic cold", "cold urticaria (diagnosis)", "Cold-induced angioedema-urticaria", "primary idiopathic cold urticaria", "Cold-induced angio-edema-urticaria", "Cold-induced angio-oedema-urticaria", "Urticaria caused by cold (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cold urticaria", "shortest_name_length": 14}
{"curie": "UMLS:C4521636", "names": ["Stage IVC Laryngeal Throat Cancer", "Stage IVC Laryngeal Cancer AJCC v8", "Stage IVC Laryngeal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Laryngeal Cancer AJCC v8", "shortest_name_length": 33}
{"curie": "UMLS:C2347754", "names": ["Spinal Cord Tumor", "adult spinal cord tumor", "Adult Spinal Cord Tumor", "Spinal cord tumor, adult", "adult spinal cord neoplasm", "Adult Spinal Cord Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Spinal Cord Neoplasm", "shortest_name_length": 17}
{"curie": "UMLS:C5670726", "names": ["Systemic Mastocytosis Associated with Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Systemic Mastocytosis Associated with Germ Cell Tumor", "shortest_name_length": 53}
{"curie": "UMLS:C5442630", "names": ["Bone Cement Implantation Syndrome", "Bone cement implantation syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone cement implantation syndrome", "shortest_name_length": 33}
{"curie": "MONDO:0004484", "names": ["Gallbladder Melanoma", "gallbladder melanoma", "gall bladder melanoma", "melanoma of gallbladder", "Melanoma of Gallbladder", "Melanoma of the Gallbladder", "melanoma of the gallbladder", "gallbladder malignant melanoma", "Gallbladder Malignant Melanoma", "gall bladder melanoma (disease)", "Malignant Melanoma of Gallbladder", "malignant melanoma of gallbladder", "melanoma (disease) of gall bladder", "melanoma of gallbladder (diagnosis)", "malignant melanoma of the gallbladder", "Malignant Melanoma of the Gallbladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gallbladder melanoma", "shortest_name_length": 20}
{"curie": "MONDO:0011908", "names": ["jmml", "JMML", "JCML", "Chronic Myelomonocytic Leukemia", "chronic myelomonocytic leukemia", "JUVENILE MYELOMONOCYTIC LEUKEMIA", "juvenile myelomonocytic leukemia", "Juvenile myelomonocytic leukemia", "leukemia juvenile myelomonocytic", "leukemia, chronic myelomonocytic", "Juvenile Myelomonocytic Leukemia", "leukemia, juvenile myelomonocytic", "Juvenile chronic myeloid leukemia", "juvenile chronic myeloid leukemia", "LEUKEMIA, JUVENILE MYELOMONOCYTIC", "Leukemia, Juvenile Myelomonocytic", "Juvenile Myelomonocytic Leukemias", "Myelomonocytic Leukemia, Juvenile", "myelomonocytic leukemia, juvenile", "Juvenile myelomonocytic leukaemia", "Juvenile Chronic Myeloid Leukemia", "Juvenile chronic myeloid leukaemia", "Leukemia, Myelomonocytic, Juvenile", "Myelomonocytic Leukemias, Juvenile", "Juvenile myelomonocytic leukemia NOS", "juvenile chronic myelogenous leukemia", "Juvenile Chronic Myelogenous Leukemia", "juvenile myelomonocytic leukemia (JMML)", "Juvenile chronic myelomonocytic leukemia", "JCML - Juvenile chronic myeloid leukemia", "juvenile chronic myelomonocytic leukemia", "JCML - Juvenile chronic myeloid leukaemia", "Juvenile chronic myelomonocytic leukaemia", "leukemia, juvenile myelomonocytic, somatic", "Juvenile myelomonocytic leukemia (disorder)", "Juvenile chronic myeloid leukemia (disorder)", "juvenile myelomonocytic leukemia (diagnosis)", "Juvenile chronic myeloid leukemia (diagnosis)", "Juvenile myelomonocytic leukemia (morphologic abnormality)", "juvenile myelomonocytic leukemia, autosomal dominant, somatic mutation", "leukemia, juvenile myelomonocytic, autosomal dominant, somatic mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile myelomonocytic leukemia", "shortest_name_length": 4}
{"curie": "UMLS:C1335015", "names": ["Non-Neoplastic Heart Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Heart Disorder", "shortest_name_length": 29}
{"curie": "MONDO:0018507", "names": ["microcephaly-complex motor and sensory axonal neuropathy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly-complex motor and sensory axonal neuropathy syndrome", "shortest_name_length": 65}
{"curie": "MONDO:0012795", "names": ["hypophosphatemic rickets and hyperparathyroidism", "HYPOPHOSPHATEMIC RICKETS AND HYPERPARATHYROIDISM", "Hypophosphatemic Rickets And Hyperparathyroidism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypophosphatemic rickets and hyperparathyroidism", "shortest_name_length": 48}
{"curie": "MONDO:0012266", "names": ["PEE4", "STOX1 preeclampsia", "Preeclampsia Eclampsia 4", "preeclampsia/eclampsia 4", "PREECLAMPSIA/eclampsia 4", "PREECLAMPSIA/ECLAMPSIA 4", "Preeclampsia/eclampsia type 4", "preeclampsia caused by mutation in STOX1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "preeclampsia/eclampsia 4", "shortest_name_length": 4}
{"curie": "UMLS:C1709571", "names": ["Pleural Biphasic Synovial Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pleural Biphasic Synovial Sarcoma", "shortest_name_length": 33}
{"curie": "UMLS:C1699741", "names": ["Intraoperative Head and Neck Injury", "intraoperative head and neck injury", "Intraoperative head and neck injury", "intraoperative head and neck injury (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraoperative Head and Neck Injury", "shortest_name_length": 35}
{"curie": "UMLS:C1336399", "names": ["Stage IVC Nasopharynx Carcinoma", "Stage IVC Carcinoma of Nasopharynx", "Stage IVC Nasopharyngeal Carcinoma", "Stage IVC Nasopharyngeal Throat Cancer", "Stage IVC Carcinoma of the Nasopharynx", "Stage IVC Nasopharyngeal Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Nasopharyngeal Carcinoma AJCC v7", "shortest_name_length": 31}
{"curie": "MONDO:0006683", "names": ["Brachial plexopathy", "brachial plexopathy", "Brachial Plexopathy", "Plexopathy, Brachial", "brachial plexopathies", "Plexopathies, Brachial", "Brachial Plexus Disease", "Plexus Disease, Brachial", "Brachial plexus disorder", "Brachial Plexus Disorder", "Brachial Plexus Diseases", "brachial plexus disorder", "brachial plexus; syndrome", "Plexus Disorder, Brachial", "Brachial Plexus Disorders", "syndrome; brachial plexus", "Brachial plexus--Diseases", "Plexus Diseases, Brachial", "Brachial plexus disorders", "Plexus Disorders, Brachial", "brachial plexus neuropathy", "Brachial plexus neuropathy", "BRACHIAL PLEXUS NEUROPATHY", "Brachial Plexus Neuropathy", "neuropathy; brachial plexus", "Neuropathy, Brachial Plexus", "brachial plexus; neuropathy", "Plexus Neuropathy, Brachial", "Brachial Plexus Neuropathies", "Neuropathies, Brachial Plexus", "Plexus Neuropathies, Brachial", "plexus brachialis; neuropathic", "Brachial plexus neuropathy, NOS", "BPN - Brachial plexus neuropathy", "Brachial plexus disorder (disorder)", "brachial plexus disorder (diagnosis)", "disease (or disorder); plexus, brachial", "brachial nerve plexus peripheral neuropathy", "peripheral neuropathy of brachial nerve plexus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachial plexus neuropathy", "shortest_name_length": 19}
{"curie": "MONDO:0004886", "names": ["diffuse secondary choroid atrophy", "Diffuse secondary choroid atrophy", "diffuse secondary choroidal atrophy", "Diffuse secondary atrophy of choroid", "Diffuse secondary choroid atrophy (disorder)", "diffuse secondary choroidal atrophy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diffuse secondary choroid atrophy", "shortest_name_length": 33}
{"curie": "UMLS:C0235889", "names": ["Arthritis aggravated", "Aggravated Arthritis", "ARTHRITIS AGGRAVATED", "Arthritis NOS aggravated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arthritis NOS aggravated", "shortest_name_length": 20}
{"curie": "MONDO:0014675", "names": ["DFNB104", "autosomal recessive deafness 104", "deafness, autosomal recessive 104", "DEAFNESS, AUTOSOMAL RECESSIVE 104", "deafness, autosomal recessive type 104", "autosomal recessive nonsyndromic deafness 104", "RIPOR2 autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 104", "autosomal recessive nonsyndromic deafness type 104", "autosomal recessive nonsyndromic deafness caused by mutation in RIPOR2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 104", "shortest_name_length": 7}
{"curie": "UMLS:C0279612", "names": ["Embryonal Rhabdomyosarcoma", "Childhood Embryonal Rhabdomyosarcoma", "embryonal pediatric rhabdomyosarcoma", "embryonal childhood rhabdomyosarcoma", "Embryonal Childhood Rhabdomyosarcoma", "Pediatric Embryonal Rhabdomyosarcoma", "rhabdomyosarcoma, pediatric embryonal", "childhood rhabdomyosarcoma, embryonal", "rhabdomyosarcoma, embryonal childhood", "pediatric rhabdomyosarcoma, embryonal", "rhabdomyosarcoma, childhood embryonal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Embryonal Rhabdomyosarcoma", "shortest_name_length": 26}
{"curie": "MONDO:0001269", "names": ["Sclera Disease", "disease sclera", "sclera disease", "sclera disorder", "diseases sclera", "scleral disease", "Scleral Disease", "Disease, Sclera", "Sclera Disorder", "sclera diseases", "Sclera Diseases", "Disease, Scleral", "Scleral disorder", "scleral disorder", "scleral diseases", "Scleral Disorder", "Scleral Diseases", "Diseases, Sclera", "sclera disorders", "Diseases, Scleral", "disorders scleral", "disease of sclera", "disorder of sclera", "Disorder of sclera", "Disorders of sclera", "Scleral disorder NOS", "Disorder of sclera, NOS", "DISORDERS OF THE SCLERA", "sclera disease or disorder", "disease (or disorder); sclera", "Disorder of sclera (disorder)", "disease or disorder of sclera", "Unspecified disorder of sclera", "disorder of sclera (diagnosis)", "Disorder of sclera, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scleral disorder", "shortest_name_length": 14}
{"curie": "MONDO:0001757", "names": ["frontal sinus tumor", "Frontal Sinus Tumor", "Tumor of Frontal Sinus", "frontal sinus neoplasm", "tumor of frontal sinus", "Tumor of frontal sinus", "Frontal Sinus Neoplasm", "Tumour of frontal sinus", "Neoplasm of Frontal Sinus", "neoplasm of frontal sinus", "Neoplasm of frontal sinus", "tumor of the frontal sinus", "Tumor of the Frontal Sinus", "tumor of the Frontal sinus", "frontal sinus benign neoplasm", "Neoplasm of the Frontal Sinus", "neoplasm of the frontal sinus", "frontal sinus neoplasm (disease)", "Neoplasm of frontal sinus (disorder)", "neoplasm of frontal sinus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontal sinus neoplasm", "shortest_name_length": 19}
{"curie": "MONDO:0025303", "names": ["tick fever", "fever tick", "fevers tick", "fever ticks", "anaplasmosis", "Anaplasmosis", "Anaplasmoses", "Gallsickness", "ANAPLASMOSES", "Anaplasmosis, NOS", "Anaplasma Infection", "Anaplasma Infections", "Infection, Anaplasma", "Infections, Anaplasma", "Anaplasmosis (disorder)", "Infection due to Anaplasma", "anaplasma infectious disease", "anaplasma disease or disorder", "Anaplasma phagocytophilum Infection", "anaplasma caused disease or disorder", "Anaplasma phagocytophilum Infections"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anaplasmosis", "shortest_name_length": 10}
{"curie": "MONDO:0009156", "names": ["Ectrodactyly-Polydactyly", "ECTRODACTYLY-POLYDACTYLY", "ectrodactyly-polydactyly", "ectrodactyly polydactyly", "ectrodactyly-polydactyly syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectrodactyly-polydactyly syndrome", "shortest_name_length": 24}
{"curie": "UMLS:C4285106", "names": ["FIGO Stage II Ovarian Cancer", "FIGO Stage II Ovarian Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Stage II Ovarian Cancer", "shortest_name_length": 28}
{"curie": "UMLS:C1333972", "names": ["Liver MALToma", "Hepatic MALToma", "MALToma of Liver", "MALT Liver Lymphoma", "MALToma of the Liver", "MALT Hepatic Lymphoma", "MALT Lymphoma of Liver", "MALT Lymphoma of the Liver", "Liver Mucosa-Associated Lymphoid Tissue Lymphoma", "Mucosa-Associated Lymphoid Tissue Liver Lymphoma", "Hepatic Mucosa-Associated Lymphoid Tissue Lymphoma", "Mucosa-Associated Lymphoid Tissue Lymphoma of Liver", "Mucosa-Associated Lymphoid Tissue Lymphoma of the Liver"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liver Mucosa-Associated Lymphoid Tissue Lymphoma", "shortest_name_length": 13}
{"curie": "UMLS:C1336256", "names": ["Stage III Nasal Cavity Cancer", "Stage III Nasal Cavity Carcinoma", "Stage III Carcinoma of Nasal Cavity", "Stage III Carcinoma of the Nasal Cavity", "Stage III Nasal Cavity Carcinoma AJCC v6", "Stage III Nasal Cavity Carcinoma AJCC v7", "Stage III Nasal Cavity Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Nasal Cavity Cancer AJCC v6 and v7", "shortest_name_length": 29}
{"curie": "UMLS:C0021290", "names": ["Neonatal disease", "neonatal disease", "disease neonatal", "Neonatal Disease", "NEONATAL DISORDER", "Disease, Neonatal", "Neonatal Diseases", "Neonatal disorder", "Neonatal Disorder", "DISORDER NEONATAL", "diseases neonatal", "neonatal disorders", "Neonatal Disorders", "Diseases, Neonatal", "Neonatal disease, NOS", "Neonatal disorder NOS", "Infant, Newborn, Diseases", "Newborn infants--Diseases", "Neonatal disorder (disorder)", "neonatal disorders (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neonatal disorder", "shortest_name_length": 16}
{"curie": "UMLS:C0854679", "names": ["Needle injury", "Needlestick Puncture", "Needle stick/puncture", "Needle Stick/Puncture"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Needle injury", "shortest_name_length": 13}
{"curie": "UMLS:C4055156", "names": ["Denys-Drash Syndrome, Incomplete"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Denys-Drash Syndrome, Incomplete", "shortest_name_length": 32}
{"curie": "UMLS:C1112758", "names": ["Infective exacerbation of chronic obstructive airways disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infective exacerbation of chronic obstructive airways disease", "shortest_name_length": 61}
{"curie": "MONDO:0001598", "names": ["Godwin Tumor", "Godwin tumor", "Benign Salivary Gland Lymphoepithelial Lesion", "Benign lymphoepithelial salivary gland lesion", "benign salivary gland lymphoepithelial lesion", "lesion; salivary gland, benign lymphoepithelial", "salivary gland; lesion, benign lymphoepithelial", "benign lymphoepithelial lesion of salivary gland", "Benign lymphoepithelial lesion of salivary gland", "Benign Lymphoepithelial Lesion of Salivary Gland", "benign lymphoepithelial lesion of the salivary gland", "Benign Lymphoepithelial Lesion of the Salivary Gland", "Benign lymphoepithelial lesion of salivary gland (disorder)", "benign lymphoepithelial lesion of salivary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign lymphoepithelial lesion of salivary gland", "shortest_name_length": 12}
{"curie": "MONDO:0011971", "names": ["HIGM5", "HIGM5 Syndrome", "HIGM5 Syndromes", "Hyper IgM Syndrome 5", "HYPER-IgM SYNDROME 5", "hyper IgM syndrome 5", "Hyper-IgM Syndrome 5", "hyper-IgM syndrome 5", "Hyper-IgM Syndrome 5s", "UNG hyper-IgM syndrome", "hyper-IgM syndrome type 5", "Hyper-IgM syndrome type 5", "immunodeficiency with hyper IgM type 5", "immunodeficiency with hyper-IgM, type 5", "IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 5", "Immunodeficiency with Hyper IgM, Type 5", "Immunodeficiency with Hyper-IgM, Type 5", "immunodeficiency with hyper IgM, type 5", "hyper-IgM syndrome due to UNG deficiency", "Hyper-IgM syndrome due to UNG deficiency", "Hyper-IgM Immunodeficiency Syndrome Type 5", "Hyper IgM Immunodeficiency Syndrome Type 5", "Hyper-IgM Immunodeficiency Syndrome, Type 5", "Hyper IgM Immunodeficiency Syndrome, Type 5", "hyper-IgM syndrome caused by mutation in UNG", "hyper-IgM syndrome due to uracil N-glycosylase", "Hyper-IgM syndrome due to uracil N-glycosylase"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyper-IgM syndrome type 5", "shortest_name_length": 5}
{"curie": "UMLS:C0242973", "names": ["Ventricular dysfunction", "dysfunction ventricular", "Ventricular Dysfunction", "ventricular dysfunction", "Dysfunction, Ventricular", "Ventricular Dysfunctions", "Dysfunctions, Ventricular"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ventricular Dysfunction", "shortest_name_length": 23}
{"curie": "UMLS:C5575689", "names": ["MBD", "Myeloma Bone Disease", "Multiple Myeloma-Induced Bone Disease", "Plasma Cell Myeloma-Induced Bone Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Plasma Cell Myeloma-Induced Bone Disease", "shortest_name_length": 3}
{"curie": "UMLS:C1336214", "names": ["Stage IIIA Retinoblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Retinoblastoma", "shortest_name_length": 25}
{"curie": "MONDO:0012675", "names": ["Cbg deficiency", "CBG deficiency", "CBG Deficiency", "CBG DEFICIENCY", "TRANSCORTIN DEFICIENCY", "transcortin deficiency", "Transcortin Deficiency", "Transcortin deficiency", "corticosteroid-binding globulin, elevated", "Corticosteroid-Binding Globulin, Elevated", "CORTICOSTEROID-BINDING GLOBULIN, ELEVATED", "Corticosteroid-Binding Globulin Deficiency", "Corticosteroid-binding globulin deficiency", "CORTICOSTEROID-BINDING GLOBULIN DEFICIENCY", "corticosteroid-binding globulin deficiency", "Corticosteroid-binding globulin deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corticosteroid-binding globulin deficiency", "shortest_name_length": 14}
{"curie": "MONDO:0008065", "names": ["nasal groove, familial transverse", "NASAL GROOVE, FAMILIAL TRANSVERSE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasal groove, familial transverse", "shortest_name_length": 33}
{"curie": "MONDO:0002613", "names": ["PERSONALITY HYSTERICAL", "Histrionic personality", "Hysterical personality", "histrionic personality", "hysterical personality", "Hysterical Personality", "HYSTERICAL PERSONALITY", "Personality, Hysterical", "Hysterical Personalities", "Personalities, Hysterical", "Hysterical personality NOS", "histionic personality disorder", "PERSONALITY DISORDER HISTRIONIC", "Histrionic personality disorder", "Hysterical personality disorder", "disorder histrionic personality", "histrionic personality disorder", "Histrionic Personality Disorder", "Disorder, Histrionic Personality", "personality disorder; hysterical", "hysterical; personality disorder", "Personality Disorder, Histrionic", "personality disorder; histrionic", "Histrionic Personality Disorders", "disorders histrionic personality", "histrionic; personality disorder", "Disorders, Histrionic Personality", "Hysterical personality (disorder)", "Personality Disorders, Histrionic", "histrionic personality disorder (disease)", "Histrionic personality disorder (disorder)", "histrionic personality disorder (diagnosis)", "Histrionic personality disorder, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "histrionic personality disorder", "shortest_name_length": 22}
{"curie": "UMLS:C3273114", "names": ["Gallbladder Adenocarcinoma, Gastric Foveolar Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gallbladder Adenocarcinoma, Gastric Foveolar Type", "shortest_name_length": 49}
{"curie": "MONDO:0023179", "names": ["fragile X syndrome type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fragile X syndrome type 2", "shortest_name_length": 25}
{"curie": "UMLS:C5206603", "names": ["Paratesticular Deep (Aggressive) Angiomyxoma", "Paratesticular Deep \"Aggressive\" Angiomyxoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paratesticular Deep (Aggressive) Angiomyxoma", "shortest_name_length": 44}
{"curie": "UMLS:C3804988", "names": ["Escherichia pyelonephritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Escherichia pyelonephritis", "shortest_name_length": 26}
{"curie": "MONDO:0012613", "names": ["MRT5", "mental retardation, autosomal recessive 5", "Mental Retardation, Autosomal Recessive 5", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5", "mental retardation, autosomal recessive type 5", "intellectual disability, autosomal recessive 5", "intellectual disability, autosomal recessive type 5", "autosomal recessive intellectual developmental disorder 5", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 5", "NSUN2 autosomal recessive non-syndromic intellectual disability", "autosomal recessive non-syndromic intellectual disability caused by mutation in NSUN2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 5", "shortest_name_length": 4}
{"curie": "MONDO:0014926", "names": ["BBS20", "BBS22", "BBS20, FORMERLY", "BARDET-BIEDL SYNDROME 20", "BARDET-BIEDL SYNDROME 22", "Bardet-Biedl syndrome 22", "IFT74 Bardet-Biedl syndrome", "Bardet-Biedl syndrome type 20", "Bardet-Biedl syndrome 20; BBS20", "BARDET-BIEDL SYNDROME 20, FORMERLY", "Bardet-Biedl syndrome caused by mutation in IFT74"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bardet-Biedl syndrome 22", "shortest_name_length": 5}
{"curie": "MONDO:0008470", "names": ["spondyloepiphyseal dysplasia, Byers type", "SPONDYLOEPIPHYSEAL DYSPLASIA WITH PUNCTATE CORNEAL DYSTROPHY", "Spondyloepiphyseal Dysplasia With Punctate Corneal Dystrophy", "spondyloepiphyseal dysplasia with punctate corneal dystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepiphyseal dysplasia with punctate corneal dystrophy", "shortest_name_length": 40}
{"curie": "MONDO:0011493", "names": ["STL2", "STL 2", "Stickler syndrome 2", "Stickler Syndrome Type 2", "Stickler syndrome type 2", "type 2 Stickler syndrome", "Stickler syndrome, type 2", "Stickler syndrome type II", "COL11A1 Stickler syndrome", "Stickler Syndrome Type II", "STICKLER SYNDROME, TYPE II", "STICKLER syndrome, type II", "Stickler Syndrome, Type II", "Stickler syndrome, vitreous type 2", "STICKLER SYNDROME, VITREOUS TYPE 2", "Stickler syndrome type 2 (disorder)", "type 2 Stickler syndrome (diagnosis)", "STICKLER SYNDROME, TYPE II (disorder)", "STICKLER SYNDROME, BEADED VITREOUS TYPE", "Stickler syndrome, beaded vitreous type", "Stickler syndrome caused by mutation in COL11A1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stickler syndrome type 2", "shortest_name_length": 4}
{"curie": "MONDO:0011531", "names": ["NS2", "Noonan syndrome 2", "Noonan Syndrome 2", "NOONAN SYNDROME 2", "Noonan syndrome type 2", "Noonan syndrome autosomal recessive", "autosomal recessive Noonan syndrome", "Noonan Syndrome, Autosomal Recessive", "Noonan syndrome, autosomal recessive", "NOONAN SYNDROME, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Noonan syndrome 2", "shortest_name_length": 3}
{"curie": "MONDO:0001902", "names": ["congenital agammaglobulinemia", "congenital hypogammaglobulinemia", "Congenital hypogammaglobulinemia", "congenital hypogammaglobulinaemia", "Congenital hypogammaglobulinaemia", "congenital hypogammaglobulinemia (finding)", "Congenital hypogammaglobulinemia (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital agammaglobulinemia", "shortest_name_length": 29}
{"curie": "UMLS:C3275112", "names": ["Mild Cardiac Valve Stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mild Cardiac Valve Stenosis", "shortest_name_length": 27}
{"curie": "MONDO:0005763", "names": ["Flavivirus Infection", "Flavivirus infection", "Flavivirus Infections", "Infection, Flavivirus", "Flaviviral infections", "Flaviviridae Infection", "Infections, Flavivirus", "Flaviviridae Infections", "Infection, Flaviviridae", "Infections, Flaviviridae", "Disease due to Flavivirus", "DISEASES DUE TO FLAVIVIRUS", "Disease due to Flaviviridae", "Disease caused by Flavivirus", "Disease due to Flavivirus, NOS", "Disease caused by Flaviviridae", "Flaviviridae infectious disease", "Flaviviridae disease or disorder", "Flaviviridae caused disease or disorder", "Disease caused by Flavivirus (disorder)", "Disease caused by Flaviviridae (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Flaviviridae infectious disease", "shortest_name_length": 20}
{"curie": "UMLS:C5205913", "names": ["Metastatic Malignant Neoplasm in the Pelvic Cavity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Malignant Neoplasm in the Pelvic Cavity", "shortest_name_length": 50}
{"curie": "MONDO:0011381", "names": ["dominant beta-thalassemia", "Dominant beta-thalassemia", "Dominant beta-thalassaemia", "BETA-THALASSEMIA, DOMINANT", "Inclusion body beta-thalassemia", "inclusion body beta-thalassemia", "Inclusion body beta-thalassaemia", "Dominant beta-thalassemia (disorder)", "autosomal dominant  beta thalassemia", "thalassemia-beta, dominant inclusion-body", "BETA-THALASSEMIA, DOMINANT INCLUSION BODY TYPE", "beta-thalassemia, dominant inclusion body type", "Beta Thalassemia, Dominant Inclusion Body Type", "DYSERYTHROPOIETIC ANEMIA, CONGENITAL, IRISH OR WEATHERALL TYPE", "Dyserythropoietic Anemia, Congenital, Irish or Weatherall Type", "dyserythropoietic Anemia, congenital, Irish or Weatherall type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dominant beta-thalassemia", "shortest_name_length": 25}
{"curie": "UMLS:C0078888", "names": ["AIVR", "aivr", "Slow Ventricular Tachycardia", "Slow Ventricular Tachycardias", "Ventricular Tachycardia, Slow", "Ventricular Tachycardias, Slow", "Accelerated idioventricular rhythm", "ACCELERATED IDIOVENTRICULAR RHYTHM", "Accelerated Idioventricular Rhythm", "accelerated idioventricular rhythm", "Accelerated Idioventricular Rhythms", "Idioventricular Rhythm, Accelerated", "Idioventricular Rhythms, Accelerated", "accelerated idioventricular rhythm (AIVR)", "Accelerated idioventricular rhythm (disorder)", "accelerated idioventricular rhythm (diagnosis)", "Accelerated Idioventricular Rhythm by ECG Finding", "Accelerated Idioventricular Rhythm by EKG Finding"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Accelerated Idioventricular Rhythm", "shortest_name_length": 4}
{"curie": "MONDO:0022573", "names": ["biliary atresia intrahepatic non syndromic form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "biliary atresia intrahepatic non syndromic form", "shortest_name_length": 47}
{"curie": "UMLS:C4303254", "names": ["Breast Solid Papillary Carcinoma In Situ", "Solid papillary carcinoma in situ of breast", "Solid papillary carcinoma in situ of breast (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Solid papillary carcinoma in situ of breast", "shortest_name_length": 40}
{"curie": "MONDO:0000632", "names": ["benign uterus tumor", "Benign Uterus Tumor", "benign uterus tumors", "Benign Uterine Tumor", "benign uterine tumor", "Benign Uterus Tumors", "benign uterine tumors", "Benign Uterine Tumors", "Benign Uterus Neoplasm", "benign tumor of uterus", "Neoplasm benign;uterus", "Benign Tumor of Uterus", "benign uterus neoplasm", "Benign tumor of uterus", "uterus benign neoplasm", "Uterous Tumors, Benign", "Uterine Tumors, Benign", "Uterous tumors, benign", "uterine tumors, benign", "Benign uterine neoplasm", "BENIGN UTERINE NEOPLASM", "uterine benign neoplasm", "benign uterus neoplasms", "benign uterine neoplasm", "Benign tumour of uterus", "Benign Uterus Neoplasms", "Benign Uterine Neoplasm", "benign uterine neoplasms", "Uterine neoplasms benign", "uterine neoplasm, benign", "Benign Uterine Neoplasms", "uterine neoplasms, benign", "Benign neoplasm of uterus", "Uterine Neoplasms, Benign", "benign neoplasm of uterus", "Uterous neoplasms, benign", "Uterous Neoplasms, Benign", "Benign Neoplasm of Uterus", "benign tumor of the uterus", "Benign Tumor of the Uterus", "Benign Uterine Neoplasm NOS", "Benign uterine neoplasm NOS", "Benign Neoplasm of the Uterus", "benign neoplasm of the uterus", "Benign neoplasm of uterus, NOS", "Benign neoplasm of uterus (disorder)", "benign neoplasm of uterus (diagnosis)", "Benign neoplasm of uterus, part unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine benign neoplasm", "shortest_name_length": 19}
{"curie": "UMLS:C1504457", "names": ["Implant site urticaria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Implant site urticaria", "shortest_name_length": 22}
{"curie": "UMLS:C1336435", "names": ["Stage IV Mesothelioma", "stage IV pleural mesothelioma", "stage IV malignant mesothelioma", "stage IV mesothelioma of pleura", "Stage IV Mesothelioma of Pleura", "Stage IV Mesothelioma of the Pleura", "stage IV mesothelioma of the pleura", "stage IV pleural mesothelioma AJCC v7", "Stage IV Pleural Malignant Mesothelioma", "Stage IV Pleural Malignant Mesothelioma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Pleural Malignant Mesothelioma AJCC v7", "shortest_name_length": 21}
{"curie": "MONDO:0016922", "names": ["Duplication of chromosome 2", "partial trisomy of chromosome 2", "Partial trisomy of chromosome 2", "partial duplication of chromosome 2", "Partial duplication of chromosome 2", "partial duplication of chromosome type 2", "Partial trisomy of chromosome 2 (disorder)", "partial trisomy of chromosome 2 (diagnosis)", "anomaly of chromosome pair 2 partial trisomy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of chromosome 2", "shortest_name_length": 27}
{"curie": "MONDO:0020421", "names": ["coronary artery intramyocardial course"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coronary artery intramyocardial course", "shortest_name_length": 38}
{"curie": "MONDO:0016562", "names": ["PSP-PAGF", "PSP-pure akinesia with gait freezing", "progressive supranuclear palsy-pure akinesia with gait freezing syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive supranuclear palsy-pure akinesia with gait freezing syndrome", "shortest_name_length": 8}
{"curie": "UMLS:C0750272", "names": ["Unilateral vision loss", "VISION LOSS UNILATERAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unilateral vision loss", "shortest_name_length": 22}
{"curie": "MONDO:0007186", "names": ["ger", "GER", "GERD", "gerd", "brash", "BRASH", "reflux", "pyrosis", "Pyrosis", "Pyroses", "acidity", "PYROSIS", "Spilling", "heartburn", "HEARTBURN", "ge reflux", "GE REFLUX", "Heartburn", "HEART BURN", "acid reflux", "Acid reflux", "reflux acid", "Acid Reflux", "Spitting Up", "Infant Reflux", "Burning reflux", "gastric reflux", "GER in Infants", "Gastric reflux", "Reflux Disease", "Heartburn symptom", "esophageal reflux", "ESOPHAGEAL REFLUX", "reflux esophageal", "Reflux in Infants", "Esophageal Reflux", "Esophageal reflux", "Reflux;oesophageal", "oesophageal reflux", "Oesophageal reflux", "Gastric Acid Reflux", "Heartburn (finding)", "Acid reflux disease", "heartburn (symptom)", "Acid Reflux, Gastric", "Infant regurgitation", "Reflux, Gastric Acid", "Infant Regurgitation", "Heartburn/Indigestion", "Esophageal reflux NOS", "Acid reflux (finding)", "Gastresophageal reflux", "reflux gastroesophageal", "GASTROESOPHAGEAL REFLUX", "Gastroesophageal reflux", "Gastroesophageal Reflux", "gastroesophageal reflux", "gastrooesophageal reflux", "Gastrooesophageal reflux", "gastro-esophageal reflux", "Gastro-Esophageal Reflux", "Reflux, Gastroesophageal", "gastro esophageal reflux", "Gastro Esophageal Reflux", "Gastro-esophageal reflux", "reflux; gastroesophageal", "gastroesophageal; reflux", "reflux disease esophageal", "esophageal reflux disease", "Gastro-oesophageal Reflux", "Reflux, Gastro-Esophageal", "Gastro-oesophageal reflux", "Gastro oesophageal Reflux", "Esophageal reflux disease", "gastro oesophageal reflux", "gastro-oesophageal reflux", "diseases esophageal reflux", "Reflux, Gastro-oesophageal", "Gastric Acid Reflux Disease", "esophageal reflux (diagnosis)", "gastresophageal reflux disease", "GOR - Gastro-esophageal reflux", "Gastrointestinal Regurgitation", "GASTROESOPHAGEAL REFLUX DISEASE", "Gastroesophageal Reflux Disease", "gastroesophageal reflux disease", "GOR - Gastro-oesophageal reflux", "Gastroesophageal reflux disease", "Gastro Esophageal Reflux Disease", "Gastrooesophageal reflux disease", "gastrooesophageal reflux disease", "gastro-esophageal reflux disease", "Gastro-esophageal reflux disease", "Gastro-Esophageal Reflux Disease", "disease gastro-esophageal reflux", "Gastro-Esophageal Reflux Diseases", "Reflux Disease, Gastro-Esophageal", "Gastro-oesophageal reflux disease", "Pediatric Gastroesophageal Reflux", "Infantile Gastroesophageal Reflux", "GASTROESOPHAGEAL REFLUX, PEDIATRIC", "gastroesophageal reflux, pediatric", "Infant gastrointestinal regurgitation", "gastroesophageal reflux disease (GERD)", "GORD - Gastro-esophageal reflux disease", "GERD - Gastro-esophageal reflux disease", "GERD - gastro-esophageal reflux disease", "GORD - Gastro-oesophageal reflux disease", "Gastroesophageal reflux disease (disorder)", "Infant gastrointestinal regurgitation (finding)", "CARDIOESOPHAGEAL RELAXATION, GASTROESOPHAGEAL REFLUX"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastroesophageal reflux disease", "shortest_name_length": 3}
{"curie": "MONDO:0004165", "names": ["Selective IgD deficiency", "selective IgD immunodeficiency", "Selective IgD Immunodeficiency", "selective IgD deficiency disease", "Selective immunoglobulin D deficiency", "selective immunoglobulin D deficiency", "Selective immunoglobulin D deficiency (disorder)", "Selective immunoglobulin D deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "selective IgD deficiency disease", "shortest_name_length": 24}
{"curie": "MONDO:0015528", "names": ["Neumann tumor", "Congenital Epulis", "Congenital epulis", "congenital epulis", "Gingival Neoplasms", "Epulis, Congenital", "congenital Epulides", "Congenital Epulides", "Epulides, Congenital", "Congenital myoblastoma", "gingival granular cell tumor", "Gingival Granular Cell Tumor", "Congenital Granular Cell Tumor", "Congenital granular cell tumor", "congenital gingival cell tumor", "congenital granular cell tumor", "Congenital gingival cell tumor", "Congenital gingival granular cell tumor", "Congenital gingival granular cell tumour", "Congenital gingival granular cell tumor (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital epulis", "shortest_name_length": 13}
{"curie": "MONDO:0014634", "names": ["SRXY10", "46XY sex reversal 10", "46,XY SEX reversal 10", "46,XY SEX REVERSAL 10", "46,XY sex reversal 10", "46,XY Sex reversal type 10", "CHROMOSOME 17q24 DELETION SYNDROME", "chromosome 17q24 deletion syndrome", "chromosome 17Q24 deletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XY sex reversal 10", "shortest_name_length": 6}
{"curie": "MONDO:0014861", "names": ["ADMIO2", "autoimmune disease, multisystem, infantile-onset, 2", "AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2", "ZAP70 autoimmune disease, multisystem, infantile-onset", "autoimmune disease, multisystem, infantile-onset, type 2", "autoimmune disease, multisystem, infantile-onset, 2; ADMIO2", "autoimmune disease, multisystem, infantile-onset caused by mutation in ZAP70"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune disease, multisystem, infantile-onset, 2", "shortest_name_length": 6}
{"curie": "MONDO:0014051", "names": ["MC4DN6", "CEMCOX2", "COX15 fatal infantile encephalocardiomyopathy", "mitochondrial complex IV deficiency nuclear type 6", "MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 6", "mitochondrial complex IV deficiency, nuclear type 6", "fatal infantile encephalocardiomyopathy caused by mutation in COX15", "fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 2", "CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 2", "cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2", "cardioencephalomyopathy, fatal infantile, due to cytochrome C oxidase deficiency type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2", "shortest_name_length": 6}
{"curie": "MONDO:0014379", "names": ["HVDAS", "MRD28", "ADNP Syndrome", "ADNP syndrome", "MRD28, FORMERLY", "HELSMOORTEL-VAN DER AA SYNDROME", "Helsmoortel-VAN DER AA syndrome", "Helsmoortel-Van Der AA Syndrome", "Helsmoortel-van der Aa syndrome", "Helsmoortel-Van Der Aa Syndrome", "autosomal dominant mental retardation 28", "Autosomal Dominant Mental Retardation 28", "Mental Retardation, Autosomal Dominant 28", "mental retardation, autosomal dominant 28", "autosomal dominant intellectual disability 28", "intellectual disability, autosomal dominant 28", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 28, FORMERLY", "ADNP-related syndromic intellectual disability-autism spectrum disorder", "ADNP-related multiple congenital anomalies, intellectual disability, autism spectrum disorder", "ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder", "activity dependent neuroprotector homeobox related multiple congenital anomalies, intell disability, autism spectrum disorder", "Activity dependent neuroprotector homeobox related multiple congenital anomalies, intellectual disability, autism spectrum disorder", "activity dependent neuroprotector homeobox related multiple congenital anomalies, intell disability, autism spectrum disorder (diagnosis)", "Activity dependent neuroprotector homeobox related multiple congenital anomalies, intellectual disability, autism spectrum disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder", "shortest_name_length": 5}
{"curie": "MONDO:0013132", "names": ["SPG36", "Spg36", "hereditary spastic paraplegia 36", "hereditary spastic paraplegia type 36", "autosomal dominant spastic paraplegia 36", "spastic paraplegia 36, autosomal dominant", "Spastic Paraplegia 36, Autosomal Dominant", "SPASTIC PARAPLEGIA 36, AUTOSOMAL DOMINANT", "Autosomal dominant spastic paraplegia type 36", "autosomal dominant spastic paraplegia type 36", "Autosomal dominant spastic paraplegia type 36 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 36", "shortest_name_length": 5}
{"curie": "MONDO:0011192", "names": ["DFNB18", "DFNB18A", "Deafness, Autosomal Recessive 18", "DEAFNESS, AUTOSOMAL RECESSIVE 18", "autosomal recessive deafness 18A", "deafness, autosomal recessive 18", "deafness, autosomal recessive 18a", "deafness, autosomal recessive 18A", "DEAFNESS, AUTOSOMAL RECESSIVE 18A", "deafness, autosomal recessive type 18A", "autosomal recessive nonsyndromic deafness 18A", "USH1C autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 18A", "autosomal recessive nonsyndromic deafness type 18A", "autosomal recessive nonsyndromic deafness caused by mutation in USH1C"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 18A", "shortest_name_length": 6}
{"curie": "MONDO:0012279", "names": ["congenital muscular dystrophy merosin-positive", "Muscular Dystrophy, Congenital, Merosin-Positive", "muscular dystrophy, congenital, merosin-POSITIVE", "MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital muscular dystrophy merosin-positive", "shortest_name_length": 46}
{"curie": "MONDO:0032659", "names": ["CMCU", "mucocutaneous ulceration, chronic", "MUCOCUTANEOUS ULCERATION, CHRONIC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucocutaneous ulceration, chronic", "shortest_name_length": 4}
{"curie": "UMLS:C3897535", "names": ["Stage IIC Rectal Cancer", "Stage IIC Rectal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIC Rectal Cancer AJCC v7", "shortest_name_length": 23}
{"curie": "MONDO:0019248", "names": ["Sialidosis", "Sialidoses", "Mucolipidosis", "mucolipidosis", "Mucolipidoses", "mucolipidoses", "Mucolipidosis, NOS", "Mucolipidosis (disorder)", "mucolipidosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucolipidosis", "shortest_name_length": 10}
{"curie": "MONDO:0015034", "names": ["lissencephaly with cerebellar hypoplasia type A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lissencephaly with cerebellar hypoplasia type A", "shortest_name_length": 47}
{"curie": "MONDO:0003677", "names": ["Lateral myocardial infarction", "lateral myocardial infarction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lateral myocardial infarction", "shortest_name_length": 29}
{"curie": "MONDO:0013064", "names": ["SYNS3", "MULTIPLE SYNOSTOSES SYNDROME 3", "multiple synostoses syndrome 3", "Multiple Synostoses Syndrome 3", "FGF9 multiple synostoses syndrome", "multiple synostoses syndrome type 3", "multiple synostoses syndrome caused by mutation in FGF9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple synostoses syndrome 3", "shortest_name_length": 5}
{"curie": "MONDO:0033655", "names": ["MC4DN20", "mitochondrial complex 4 deficiency, nuclear type 20", "mitochondrial complex IV deficiency, nuclear type 20", "MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 20"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 4 deficiency, nuclear type 20", "shortest_name_length": 7}
{"curie": "UMLS:C4330688", "names": ["Miniature Adult Form of AHC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Miniature Adult Form of AHC", "shortest_name_length": 27}
{"curie": "MONDO:0019294", "names": ["mixed dermis disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed dermis disorder", "shortest_name_length": 21}
{"curie": "MONDO:0008613", "names": ["TUFTSIN DEFICIENCY", "tuftsin deficiency", "Tuftsin deficiency", "Tuftsin Deficiency", "Tuftsin deficiency (disorder)", "tuftsin deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tuftsin deficiency", "shortest_name_length": 18}
{"curie": "MONDO:0004444", "names": ["bladder tubulo-cystic clear cell adenocarcinoma", "Bladder Tubulo-Cystic Clear Cell Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder tubulo-cystic clear cell adenocarcinoma", "shortest_name_length": 47}
{"curie": "MONDO:0014503", "names": ["SCAR17", "autosomal recessive spinocerebellar ataxia 17", "spinocerebellar ataxia, autosomal recessive 17", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 17", "autosomal recessive spinocerebellar ataxia type 17", "Spinocerebellar ataxia autosomal recessive type 17", "spinocerebellar ataxia autosomal recessive type 17", "spinocerebellar ataxia, autosomal recessive type 17", "CWF19L1 autosomal recessive congenital cerebellar ataxia", "SCAR17 - spinocerebellar ataxia autosomal recessive type 17", "Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency", "autosomal recessive cerebellar ataxia due to CWF19L1 deficiency", "autosomal recessive congenital cerebellar ataxia caused by mutation in CWF19L1", "Autosomal recessive cerebellar ataxia due to CWF19 like cell cycle control factor 1 deficiency", "Autosomal recessive cerebellar ataxia due to CWF19 like cell cycle control factor 1 deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive spinocerebellar ataxia 17", "shortest_name_length": 6}
{"curie": "UMLS:C4279912", "names": ["Chemically-Induced Liver Toxicity", "Chemically Induced Liver Toxicity", "Toxicity, Chemically-Induced Liver", "Liver Toxicity, Chemically-Induced", "Chemically-Induced Liver Toxicities", "Liver Toxicities, Chemically-Induced", "Toxicities, Chemically-Induced Liver"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chemically-Induced Liver Toxicity", "shortest_name_length": 33}
{"curie": "UMLS:C1699812", "names": ["anastomotic leak uterus", "Uterine anastomotic leak", "Uterine Anastomotic Leakage", "Uterine anastomotic leak (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Anastomotic Leakage", "shortest_name_length": 23}
{"curie": "MONDO:0008877", "names": ["Drummond syndrome", "blue diaper syndrome", "Blue diaper syndrome", "BLUE DIAPER SYNDROME", "blue diaper; syndrome", "syndrome; blue diaper", "Tryptophan malabsorption syndrome", "Tryptophan malabsorption syndrome (disorder)", "Familial hypercalcemia-nephrocalcinosis-indicanuria syndrome", "familial hypercalcemia-nephrocalcinosis-indicanuria syndrome", "hypercalcemia, familial, with nephrocalcinosis and indicanuria", "HYPERCALCEMIA, FAMILIAL, WITH NEPHROCALCINOSIS AND INDICANURIA", "Hypercalcemia, familial, with nephrocalcinosis and indicanuria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blue diaper syndrome", "shortest_name_length": 17}
{"curie": "MONDO:0002988", "names": ["cervix melanoma", "Cervical Melanoma", "cervical melanoma", "Melanoma of the Cervix", "melanoma of the cervix", "primary malignant melanoma of the cervix uteri", "primary malignant melanoma of the uterine cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervix melanoma", "shortest_name_length": 15}
{"curie": "UMLS:C0392378", "names": ["gum ulcer", "Gum ulcer", "gums ulcer", "gum ulcers", "ulcer; gum", "gum; ulcer", "gums ulcers", "ulcer; gingiva", "GINGIVAL ULCER", "Ulceration gum", "Gum ulceration", "Gingival ulcer", "gingiva; ulcer", "ULCERATION GUM", "gums ulceration", "Gingival ulceration", "GINGIVAL ULCERATION", "ulceration of gingiva", "Ulceration of gingivae", "Ulceration of gingivae (disorder)", "ulceration of gingiva (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ulceration of gingivae", "shortest_name_length": 9}
{"curie": "MONDO:0024531", "names": ["TAM", "TAM1", "tubular aggregate myopathy", "Tubular aggregate myopathy", "Tubular Aggregate Myopathy", "TUBULAR AGGREGATE MYOPATHY", "Aggregate Myopathy, Tubular", "tubular aggregates myopathy", "Myopathy, Tubular Aggregate", "myopathy, tubular aggregate", "MYOPATHY, TUBULAR AGGREGATE", "Tubular Aggregate Myopathies", "Myopathies, Tubular Aggregate", "Aggregate Myopathies, Tubular", "myopathy, tubular aggregate, 1", "MYOPATHY, TUBULAR AGGREGATE, 1", "STIM1 tubular aggregate myopathy", "myopathy with tubular aggregates", "Myopathy with tubular aggregates", "Myopathy with tubular aggregates (disorder)", "tubular aggregate myopathy caused by mutation in STIM1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy, tubular aggregate, 1", "shortest_name_length": 3}
{"curie": "UMLS:C0302295", "names": ["Rash", "Exanthem", "eruption", "Eruption", "Eruptions", "ERUPTIONS", "Exanthema", "eruptions", "Eruption, NOS", "Eruption (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eruptions", "shortest_name_length": 4}
{"curie": "MONDO:0011128", "names": ["SHS", "FSSV", "DA2B", "Sheldon-Hall syndrome", "SHELDON-HALL SYNDROME", "Sheldon-hall syndrome", "Freeman Sheldon variant", "distal arthrogryposis type 2B", "arthrogryposis distal type 2b", "Distal arthrogryposis type 2B", "ARTHROGRYPOSIS, DISTAL, TYPE 2B", "arthrogryposis, distal, type 2B", "Arthrogryposis, distal, type 2b", "Freeman-Sheldon Syndrome Variant", "Freeman-Sheldon syndrome variant", "FREEMAN-SHELDON SYNDROME VARIANT", "Freeman Sheldon syndrome, variant", "Distal arthrogryposis type 2B (disorder)", "arthrogryposis distal type 2b (diagnosis)", "Arthrogryposis multiplex congenita type 2B", "arthrogryposis multiplex congenita distal type 2B", "ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE 2B", "arthrogryposis multiplex congenita, distal, type 2B", "Arthrogryposis multiplex congenita, distal, type 2b", "arthrogryposis multiplex congenita distal type II with craniofacial abnormalities", "arthrogryposis multiplex congenita, distal, type II, with craniofacial abnormalities", "Arthrogryposis Multiplex Congenita, Distal, Type II, with Craniofacial Abnormalities", "ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE II, WITH CRANIOFACIAL ABNORMALITIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sheldon-hall syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0003240", "names": ["THYROID DISEASE", "thyroid disease", "Thyroid disease", "Thyroid Disease", "abnormal thyroid", "thyroid diseases", "THYROID ABNORMAL", "thyroid disorder", "Thyroid disorder", "DISORDER THYROID", "Disease, Thyroid", "Thyroid Diseases", "thyroid abnormal", "Thyroid Disorder", "Disorder thyroid", "THYROID DISORDER", "Thyroid disorders", "thyroid disorders", "Thyroid Disorders", "thyroid; disorder", "Diseases, Thyroid", "Thyroid abnormality", "THYROID DISEASE, NOS", "Thyroid disorder NOS", "Thyroid Gland Disease", "thyroid gland disease", "Thyroid disorder, NOS", "Thyroid abnormalities", "Thyroid Gland Disorder", "thyroid gland diseases", "thyroid gland disorder", "Thyroid Gland Diseases", "Thyroid Gland Disorders", "Thyroid gland--Diseases", "Thyroid gland disorders", "thyroid gland disorders", "disease of thyroid gland", "Disease of thyroid gland", "disorder of thyroid gland", "Disorder of thyroid gland", "Diseases of Thyroid Gland", "DISORDERS OF THYROID GLAND", "Disorders of thyroid gland", "thyroid disorder (diagnosis)", "DISEASES OF THE THYROID GLAND", "diseases of the thyroid gland", "Diseases of the thyroid gland", "Disease of thyroid gland, NOS", "Disorder of thyroid gland, NOS", "disease (or disorder); thyroid", "Unspecified disorder of thyroid", "Disorder of thyroid, unspecified", "Abnormality of the thyroid gland", "thyroid gland disease or disorder", "Disorders of thyroid gland (E00-E07)", "disease or disorder of thyroid gland", "Disorder of thyroid gland (disorder)", "HYPOTHYROIDISM, HYPERTHYROIDISM AND OTHER DISORDERS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid gland disorder", "shortest_name_length": 15}
{"curie": "UMLS:C3160827", "names": ["Exposed bone in jaw"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Exposed bone in jaw", "shortest_name_length": 19}
{"curie": "MONDO:0100496", "names": ["Emery-Dreifuss-like muscular dystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Emery-Dreifuss-like muscular dystrophy", "shortest_name_length": 38}
{"curie": "MONDO:0002855", "names": ["ectomesenchymoma", "Ectomesenchymoma", "Gangliorhabdomyosarcoma", "Malignant Ectomesenchymoma", "malignant ectomesenchymoma", "Rhabdomyosarcoma with ganglionic differentiation", "rhabdomyosarcoma with ganglionic differentiation", "Sarcoma with Ganglionic or Neuroectodermal Differentiation", "sarcoma with ganglionic or neuroectodermal differentiation", "rhabdomyosarcoma with ganglionic differentiation (diagnosis)", "Rhabdomyosarcoma with ganglionic differentiation (morphologic abnormality)", "rhabdomyosarcoma with ganglionic differentiation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectomesenchymoma", "shortest_name_length": 16}
{"curie": "MONDO:0004199", "names": ["Vulvar Keratinizing Squamous Cell Carcinoma", "vulvar keratinizing squamous cell carcinoma", "keratinizing squamous cell carcinoma of vulva", "keratinizing squamous cell carcinoma of vulva (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar keratinizing squamous cell carcinoma", "shortest_name_length": 43}
{"curie": "UMLS:C0549201", "names": ["asteatosis", "Asteatosis", "Winter itch", "winter itch", "winter; itch", "itch; winter", "winter eczema", "Winter eczema", "eczema xerotic", "xerotic eczema", "Xerotic eczema", "Eczema craquelé", "eczema craquele", "Eczema craquele", "eczema; dry skin", "Prurigo hiemalis", "dry skin; eczema", "Eczema asteatotic", "ECZEMA ASTEATOTIC", "eczema asteatotic", "Asteatotic eczema", "Pruritus hiemalis", "asteatotic eczema", "pruritus hiemalis", "Pruritus, hiemalis", "Acquired xeroderma", "acquired; xeroderma", "Dry skin dermatitis", "dry skin dermatitis", "dermatitis dry skin", "xeroderma; acquired", "Winter itch (disorder)", "winter itch (diagnosis)", "Senile asteatotic eczema", "Asteatotic eczema (disorder)", "Dry skin dermatitis (disorder)", "Dry skin dermatitis (diagnosis)", "Senile asteatotic eczema (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Asteatotic eczema", "shortest_name_length": 10}
{"curie": "UMLS:C5237338", "names": ["Retroperitoneal Pain Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retroperitoneal Pain Syndrome", "shortest_name_length": 29}
{"curie": "MONDO:0017346", "names": ["EBV-Positive DLBCL, NOS", "EBV-positive DLBCL of the elderly", "Epstein-Barr Virus Positive DLBCL, NOS", "EBV-Positive Diffuse Large B-Cell Lymphoma, NOS", "EBV-Positive diffuse large B-cell lymphoma, NOS", "EBV Positive diffuse large B-cell lymphoma of the elderly", "EBV positive diffuse large B-cell lymphoma of the elderly", "EBV Positive Diffuse Large B-Cell Lymphoma of the Elderly", "Senile EBV-Associated B-Cell Lymphoproliferative Disorder", "Senile EBV-associated B-cell lymphoproliferative disorder", "Age-Related EBV Positive B-Cell Lymphoproliferative Disorder", "age-related EBV Positive B-cell lymphoproliferative disorder", "EBV-Positive Diffuse Large B-Cell Lymphoma, Not Otherwise Specified", "Epstein-Barr virus positive diffuse large B-cell lymphoma of elderly", "Epstein-Barr virus-positive diffuse large B-cell lymphoma of the elderly", "Epstein-Barr Virus Positive Diffuse Large B-Cell Lymphoma of the Elderly", "Epstein-Barr Virus Positive diffuse large B-cell lymphoma of the elderly", "Epstein-Barr virus positive diffuse large B-cell lymphoma of elderly (disorder)", "Epstein-Barr virus positive diffuse large B-cell lymphoma of elderly (diagnosis)", "Epstein-Barr Virus-Positive Diffuse Large B-Cell Lymphoma, Not Otherwise Specified", "Epstein-Barr virus positive diffuse large B-cell lymphoma of elderly (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epstein-Barr virus-positive diffuse large B-cell lymphoma of the elderly", "shortest_name_length": 23}
{"curie": "MONDO:0009940", "names": ["PYCD", "Pycd", "PKND", "Pyknodysostosis", "Pyknodysostoses", "PYKNODYSOSTOSIS", "pyknodysostosis", "PYCNODYSOSTOSIS", "Pycnodysostoses", "pycnodysostosis", "Pycnodysostosis", "MAROTEAUX-LAMY SYNDROME 2", "Maroteaux-Lamy syndrome II", "Pyknodysostosis (disorder)", "pyknodysostosis (diagnosis)", "Stanesco's dysostosis syndrome", "Maroteaux-Lamy pyknodysostosis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pycnodysostosis", "shortest_name_length": 4}
{"curie": "UMLS:C4727205", "names": ["Locally Advanced Soft Tissue Sarcoma, Excluding Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Soft Tissue Sarcoma, Excluding Liposarcoma", "shortest_name_length": 59}
{"curie": "UMLS:C1332457", "names": ["Bacterium-Related Cancer", "Bacterium-Related Malignancy", "Bacterium-Related Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bacterium-Related Malignant Neoplasm", "shortest_name_length": 24}
{"curie": "UMLS:C4763570", "names": ["Metastatic Non-Small Cell Squamous Lung Carcinoma", "Metastatic Squamous Non-Small Cell Lung Carcinoma", "Metastatic Lung Non-Small Cell Squamous Carcinoma", "Metastatic Non-Small Cell Squamous Lung  Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Lung Non-Small Cell Squamous Carcinoma", "shortest_name_length": 49}
{"curie": "MONDO:0009385", "names": ["HYPERLEUCINE-ISOLEUCINEMIA", "Hyperleucine-isoleucinemia", "hyperleucine-Isoleucinemia", "Hyperleucine-Isoleucinemia", "hyperleucine-isoleucinemia", "Hyperleucine-isoleucinaemia", "disorder; hyperleucine-isoleucinemia", "hyperleucine-isoleucinemia; disorder", "Hyperleucine-isoleucinemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperleucine-Isoleucinemia", "shortest_name_length": 26}
{"curie": "UMLS:C5447500", "names": ["Unresectable Glioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Glioma", "shortest_name_length": 19}
{"curie": "MONDO:0009210", "names": ["Owren", "Owren disease", "OWREN DISEASE", "Owren Disease", "Owrens Disease", "Disease, Owren", "Parahemophilia", "parahemophilia", "PARAHEMOPHILIA", "Parahaemophilia", "owren's disease", "Owren's disease", "Owren's Disease", "Parahemophilias", "Disease, Owren's", "deficiency, labile", "Deficiency, labile", "Factor V Deficiency", "Factor 5 Deficiency", "factor v deficiency", "factor 5 deficiency", "FACTOR V DEFICIENCY", "Factor V deficiency", "factor V deficiency", "deficiency factor v", "Owren Parahemophilia", "OWREN PARAHEMOPHILIA", "Deficiency, factor V", "Deficiency, Factor V", "Deficiency, Factor 5", "Parahemophilia, Owren", "Factor 5 Deficiencies", "Factor V Deficiencies", "factor v deficiencies", "Factor Five Deficiency", "Deficiencies, Factor V", "Deficiencies, Factor 5", "AC globulin deficiency", "deficiency; AC globulin", "AC globulin; deficiency", "PROACCELERIN DEFICIENCY", "Deficiency, AC globulin", "Proaccelerin deficiency", "Deficiency, Factor Five", "Factor V deficiency, NOS", "Labile factor deficiency", "LABILE FACTOR DEFICIENCY", "Labile Factor Deficiency", "deficiency; proaccelerin", "Deficiency, proaccelerin", "proaccelerin; deficiency", "labile Factor deficiency", "Factor Five Deficiencies", "labile factor deficiency", "labile factor; deficiency", "deficiency; labile factor", "Deficiencies, Factor Five", "Deficiency, Labile Factor", "Labile Factor Deficiencies", "Deficiencies, Labile Factor", "hereditary factor V deficiency", "hereditary Factor V deficiency", "Congenital factor V deficiency", "congenital factor V deficiency", "Hereditary Factor V Deficiency", "ACCELERATOR GLOBULIN DEFICIENCY", "Hereditary hypoproaccelerinemia", "FACTOR V DEFICIENCY, CONGENITAL", "Hereditary hypoproaccelerinaemia", "hereditary hypoproaccelerinaemia", "Hereditary factor V deficiency disease", "congenital factor V deficiency (diagnosis)", "Hereditary factor V deficiency disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital factor V deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0009359", "names": ["MARCH", "MARCH syndrome", "Hydranencephaly with Renal Aplasia-Dysplasia", "HYDRANENCEPHALY WITH RENAL APLASIA-DYSPLASIA", "hydranencephaly with renal aplasia-dysplasia", "multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia and hydranencephaly", "multinucleated neurons, anhydramnios, renal dysplasia, cerebellar Hypoplasia, and hydranencephaly", "MULTINUCLEATED NEURONS, ANHYDRAMNIOS, RENAL DYSPLASIA, CEREBELLAR HYPOPLASIA, AND HYDRANENCEPHALY", "multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly", "Multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome", "multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome", "Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, hydranencephaly syndrome", "Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, hydranencephaly syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C5419872", "names": ["Pancreatic Poorly Cohesive Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Poorly Cohesive Adenocarcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0018851", "names": ["multiple keratoacanthoma", "familial keratoacanthoma", "hereditary keratoacanthoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial keratoacanthoma", "shortest_name_length": 24}
{"curie": "MONDO:0025485", "names": ["FAIDS", "faids", "Feline AIDS", "aids feline", "feline aids", "AIDS, Feline", "Feline immunodeficiency virus cat disease", "feline acquired immunodeficiency syndrome", "Feline Acquired Immunodeficiency Syndrome", "Feline acquired immuno-deficiency syndrome", "Feline acquired immuno deficiency syndrome", "Feline Acquired Immuno-Deficiency Syndrome", "Feline Acquired Immune Deficiency Syndrome", "Feline acquired immune deficiency syndrome", "Feline Acquired Immuno Deficiency Syndrome", "Feline immunodeficiency virus caused cat disease", "Feline acquired immune deficiency syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "feline acquired immunodeficiency syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0007171", "names": ["ATRST1", "Atrial Standstill", "atrial standstill 1", "ATRIAL STANDSTILL 1", "GJA5 atrial standstill", "atrial standstill type 1", "ATRIAL CARDIOMYOPATHY WITH HEART BLOCK", "Atrial Cardiomyopathy with Heart Block", "atrial cardiomyopathy with heart block", "atrial standstill, digenic (GJA5/SCN5A)", "atrial standstill caused by mutation in GJA5", "Cardiomyopathy, Familial, with Conduction Disturbance", "cardiomyopathy, familial, with conduction disturbance", "CARDIOMYOPATHY, FAMILIAL, WITH CONDUCTION DISTURBANCE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial standstill 1", "shortest_name_length": 6}
{"curie": "UMLS:C0919909", "names": ["Tonic clonic jerking", "Tonic clonic movements"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tonic clonic movements", "shortest_name_length": 20}
{"curie": "MONDO:0035649", "names": ["Adult-onset Steinert disease", "Adult-onset myotonic dystrophy type 1", "adult-onset Steinert myotonic dystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult-onset Steinert myotonic dystrophy", "shortest_name_length": 28}
{"curie": "MONDO:0022782", "names": ["cleft lower lip cleft lateral canthi chorioretinal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleft lower lip cleft lateral canthi chorioretinal", "shortest_name_length": 50}
{"curie": "MONDO:0015758", "names": ["primary cutaneous T-cell lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary cutaneous T-cell lymphoma", "shortest_name_length": 33}
{"curie": "MONDO:0030502", "names": ["Tetrasomy", "tetrasomy", "Tetrasomies", "Tetrasomy (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tetrasomy", "shortest_name_length": 9}
{"curie": "MONDO:0003502", "names": ["ureter epidermoid carcinoma", "Ureter Epidermoid Carcinoma", "ureteral epidermoid carcinoma", "Ureteral Epidermoid Carcinoma", "ureteral Epidermoid carcinoma", "Ureter Squamous Cell Carcinoma", "epidermoid carcinoma of ureter", "Epidermoid Carcinoma of Ureter", "ureter squamous cell carcinoma", "Ureteral Squamous Cell Carcinoma", "ureteral squamous cell carcinoma", "squamous cell carcinoma of ureter", "Squamous Cell Carcinoma of Ureter", "Epidermoid Carcinoma of the Ureter", "epidermoid carcinoma of the ureter", "Squamous Cell Carcinoma of the Ureter", "squamous cell carcinoma of the ureter", "squamous cell carcinoma of ureter (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ureter squamous cell carcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0012665", "names": ["CTRCT33", "cataract 33", "cataract type 33", "cortical cataract 33", "cataract 33, cortical", "CATARACT 33, CORTICAL", "cataract 33, multiple types", "CATARACT 33, MULTIPLE TYPES", "Cataract, Cortical, Juvenile-Onset", "BFSP1 early-onset non-syndromic cataract", "early-onset non-syndromic cataract caused by mutation in BFSP1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 33", "shortest_name_length": 7}
{"curie": "MONDO:0019938", "names": ["ARM", "Anorectal anomaly", "Anorectal Anomaly", "anorectal anomaly", "Anomaly, Anorectal", "Anorectal anomalies", "ANORECTAL ANOMALIES", "Anorectal Anomalies", "Anomalies, Anorectal", "anorectal malformation", "Anorectal Malformation", "Anorectal anomaly, NOS", "Anorectal malformation", "Anorectal Malformations", "Malformation, Anorectal", "anorectal malformations", "Malformations, Anorectal", "[OBSOLETE] Anorectal atresia", "Anorectal anomaly (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anorectal malformation", "shortest_name_length": 3}
{"curie": "MONDO:0008739", "names": ["White matter agenesis", "Cerebral white matter agenesis", "agenesis of cerebral white matter", "AGENESIS OF CEREBRAL WHITE MATTER", "Agenesis of the cerebral white matter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "agenesis of cerebral white matter", "shortest_name_length": 21}
{"curie": "MONDO:0700032", "names": ["complete trisomy 18"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complete trisomy 18", "shortest_name_length": 19}
{"curie": "MONDO:0013993", "names": ["PCH7", "pontocerebellar hypoplasia type 7", "Pontocerebellar hypoplasia type 7", "pontocerebellar hypoplasia, type 7", "PONTOCEREBELLAR HYPOPLASIA, TYPE 7", "PCH7 - pontocerebellar hypoplasia type 7", "Congenital pontocerebellar hypoplasia type 7", "TOE1 non-syndromic pontocerebellar hypoplasia", "Congenital pontocerebellar hypoplasia type 7 (disorder)", "non-syndromic pontocerebellar hypoplasia caused by mutation in TOE1", "pontocerebellar hypoplasia-46,XY disorder of sex development syndrome", "Pontocerebellar hypoplasia-46,XY disorder of sex development syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pontocerebellar hypoplasia type 7", "shortest_name_length": 4}
{"curie": "UMLS:C1515291", "names": ["Testicular Sclerosing Sertoli Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular Sclerosing Sertoli Cell Tumor", "shortest_name_length": 40}
{"curie": "UMLS:C1710040", "names": ["Secondary FSGS", "Secondary focal segmental glomerulosclerosis", "Secondary Focal Segmental Glomerulosclerosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary focal segmental glomerulosclerosis", "shortest_name_length": 14}
{"curie": "UMLS:C1710547", "names": ["Unilateral Breast Cancer", "Unilateral Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unilateral Breast Carcinoma", "shortest_name_length": 24}
{"curie": "UMLS:C1698818", "names": ["Photodamaged skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Photodamaged skin", "shortest_name_length": 17}
{"curie": "MONDO:0022693", "names": ["cerebral calcification cerebellar hypoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral calcification cerebellar hypoplasia", "shortest_name_length": 44}
{"curie": "UMLS:C0264292", "names": ["abscess; throat", "throat; abscess", "pharynx; abscess", "abscess; pharynx", "pharyngeal abscess", "Pharyngeal abscess", "Abscess of pharynx", "Abscess of pharynx (disorder)", "pharyngeal abscess (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abscess of pharynx", "shortest_name_length": 15}
{"curie": "MONDO:0012681", "names": ["FEB7", "familial febrile seizures 7", "febrile seizures, familial, 7", "FEBRILE SEIZURES, FAMILIAL, 7", "familial febrile convulsions 7", "febrile convulsions, familial, 7", "FEBRILE CONVULSIONS, FAMILIAL, 7", "Febrile Convulsions, Familial, 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "febrile seizures, familial, 7", "shortest_name_length": 4}
{"curie": "UMLS:C1336505", "names": ["Sternal Paget Disease", "Sternal Paget's Disease", "Paget's Disease of Sternum", "Paget's Disease of the Sternum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sternal Paget Disease", "shortest_name_length": 21}
{"curie": "UMLS:C1334249", "names": ["Breast Micropapillary DCIS", "Micropapillary DCIS of Breast", "Micropapillary DCIS of the Breast", "Intraductal micropapillary carcinoma", "Micropapillary Ductal Carcinoma In Situ", "Intraductal Micropapillary Breast Carcinoma", "Breast Intraductal Micropapillary Carcinoma", "Non-Invasive Micropapillary Breast Carcinoma", "Breast Micropapillary Ductal Carcinoma In Situ", "Micropapillary Ductal Breast Carcinoma in situ", "intraductal micropapillary carcinoma of breast", "Non-Invasive Micropapillary Carcinoma of Breast", "Non-Infiltrating Micropapillary Breast Carcinoma", "Micropapillary Ductal Carcinoma in situ of Breast", "Non-Invasive Micropapillary Ductal Breast Carcinoma", "Non-Invasive Micropapillary Carcinoma of the Breast", "Non-Infiltrating Micropapillary Carcinoma of Breast", "Micropapillary Ductal Carcinoma in situ of the Breast", "Non-Invasive Micropapillary Ductal Carcinoma of Breast", "Non-Infiltrating Micropapillary Carcinoma of the Breast", "Non-Infiltrating Micropapillary Ductal Breast Carcinoma", "Non-Infiltrating Micropapillary Ductal Carcinoma of Breast", "intraductal micropapillary carcinoma of breast (diagnosis)", "Non-Invasive Micropapillary Ductal Carcinoma of the Breast", "Non-Infiltrating Micropapillary Ductal Carcinoma of the Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraductal Micropapillary Breast Carcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0029147", "names": ["SPGF33", "SPERMATOGENIC FAILURE 33", "spermatogenic failure 33"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 33", "shortest_name_length": 6}
{"curie": "MONDO:0011898", "names": ["CMT2 with Vocal Cord Paresis, Autosomal Recessive", "Charcot-Marie-Tooth disease, type 4A, axonal form", "CMT2 with vocal cord paresis, autosomal recessive", "CMT2 WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE", "CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A, AXONAL FORM", "Charcot-Marie-Tooth disease, Type 4A, axonal form", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE", "Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomal recessive", "CHARCOT-MARIE-TOOTH NEUROPATHY, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE", "Charcot-Marie-Tooth neuropathy, axonal, with vocal cord paresis, autosomal recessive", "Charcot-Marie-Tooth Neuropathy, Axonal, with Vocal Cord Paresis, Autosomal Recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomal recessive", "shortest_name_length": 49}
{"curie": "MONDO:0002685", "names": ["pediatric choroid plexus tumor", "childhood choroid plexus tumor", "childhood choroid plexus cancer", "childhood choroid plexus neoplasm", "Childhood Choroid Plexus Neoplasm", "Childhood Choroid Plexus Carcinoma", "childhood choroid plexus carcinoma", "pediatric choroid plexus carcinoma", "CNS tumor, pediatric choroid plexus", "CNS tumor, childhood choroid plexus", "choroid plexus carcinoma, childhood", "childhood brain tumor, choroid plexus", "pediatric brain tumor, choroid plexus", "brain tumor, pediatric choroid plexus", "brain tumor, childhood choroid plexus", "choroid plexus carcinoma of childhood", "central nervous system tumor, choroid plexus, childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood choroid plexus carcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0019259", "names": ["PKU", "CPKU", "Fölling", "classic PKU", "Classic PKU", "PAH deficiency", "PAH Deficiency", "PAH DEFICIENCY", "Folling Disease", "PHENYLKETONURIA", "Deficiency, PAH", "FOLLING DISEASE", "Disease, Folling", "FOELLING SYNDROME", "Phenylketonuria I", "Folling's Disease", "Folling's syndrome", "Disease, Folling's", "PKU1 - Phenylketonuria", "classic phenylketonuria", "Classic phenylketonuria", "Phenylketonuria, classic", "Classical Phenylketonuria", "Classical phenylketonuria", "Phenylketonuria, Classical", "Phenylpyruvic oligophrenia", "classical; phenylketonuria", "Phenylpyruvic Oligophrenia", "Imbecilitus phenylpyruvica", "phenylpyruvic oligophrenia", "phenylketonuria; classical", "Oligophrenia phenylpyruvica", "Oligophrenia Phenylpyruvica", "OLIGOPHRENIA, PHENYLPYRUVIC", "phenylpyruvic; oligophrenia", "OLIGOPHRENIA PHENYLPYRUVICA", "oligophrenia; phenylpyruvic", "HYPERPHENYLALANINEMIA TYPE I", "Oligophrenia (Phenylpyruvic)", "Hyperphenylalaninemia, type I", "Hyperphenylalaninaemia, type I", "Classical phenylketonuria (disorder)", "Phenylalanine Hydroxylase Deficiency", "PHENYLALANINE HYDROXYLASE DEFICIENCY", "Phenylalanine hydroxylase deficiency", "phenylalanine hydroxylase; deficiency", "deficiency; phenylalanine hydroxylase", "Deficiency, Phenylalanine Hydroxylase", "Reduced phenylalanine hydroxylase level", "PAH - Phenylalanine hydroxylase deficiency", "Severe phenylalanine hydroxylase deficiency", "Phenylalanine Hydroxylase Deficiency Disease", "Deficiency Disease, Phenylalanine Hydroxylase", "Phenylalanine Hydroxylase Deficiency Disease, Severe", "Deficiency Disease, Phenylalanine Hydroxylase, Severe"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "classic phenylketonuria", "shortest_name_length": 3}
{"curie": "UMLS:C1699685", "names": ["Infusion site nodule"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infusion site nodule", "shortest_name_length": 20}
{"curie": "MONDO:0009211", "names": ["F7 deficiency", "deficiency, stable", "factor 7 deficiency", "hypoproconvertinemia", "Factor VII Deficiency", "factor VII deficiency", "congenital factor VII deficiency", "congenital proconvertin deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital factor VII deficiency", "shortest_name_length": 13}
{"curie": "MONDO:0007251", "names": ["CMD", "CMD1", "CMPD", "Cmd1", "Cmpd", "CMPD1", "Cmpd1/Sra1", "CMPD1/SRA1", "Cmpd1 Sra1", "Sra1, Cmpd1", "Cmpd1 Sra1s", "Sra1s, Cmpd1", "campomelic dwarfism", "Campomelic Syndrome", "Campomelic syndrome", "Campomelic Dwarfism", "Campomelic dwarfism", "Syndrome, Campomelic", "Campomelic Dysplasia", "CAMPOMELIC DYSPLASIA", "Campomelic dysplasia", "Campomelic Syndromes", "Campomelic Dwarfisms", "campomelic dysplasia", "Dwarfism, Campomelic", "CAMPTOMELIC DYSPLASIA", "Dysplasia, Campomelic", "Dwarfisms, Campomelic", "Camptomelic Dysplasia", "camptomelic dysplasia", "Syndromes, Campomelic", "Camptomelic dysplasia", "Campomelic Dysplasias", "Dysplasia, Camptomelic", "Dysplasias, Campomelic", "Camptomelic Dysplasias", "Dysplasias, Camptomelic", "Camptomelic dwarfism syndrome", "ACAMPOMELIC CAMPOMELIC DYSPLASIA", "Camptomelic dysplasia (disorder)", "Acampomelic Campomelic Dysplasia", "acampomelic campomelic dysplasia", "Campomelic Dysplasia, Acampomelic", "Acampomelic Campomelic Dysplasias", "Dysplasia, Acampomelic Campomelic", "Campomelic Dysplasias, Acampomelic", "Dysplasias, Acampomelic Campomelic", "Acampomelic Campomelic Dysplasia (AQ)", "campomelic dysplasia with autosomal Sex reversal", "Campomelic dysplasia with autosomal sex reversal", "Campomelic Dysplasia with Autosomal Sex Reversal", "CAMPOMELIC DYSPLASIA WITH AUTOSOMAL SEX REVERSAL", "acampomelic campomelic dysplasia with autosomal Sex reversal", "ACAMPOMELIC CAMPOMELIC DYSPLASIA WITH AUTOSOMAL SEX REVERSAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "campomelic dysplasia", "shortest_name_length": 3}
{"curie": "MONDO:0006280", "names": ["Pneumocytoma", "sclerosing hemangioma", "Sclerosing hemangioma", "Hemangioma sclerosing", "Sclerosing haemangioma", "Haemangioma sclerosing", "sclerosing haemangioma", "Sclerosing pneumocytoma", "Lung Sclerosing Angioma", "sclerosing Pneumocytoma", "Sclerosing Pneumocytoma", "lung sclerosing angioma", "sclerosing angioma of lung", "lung sclerosing hemangioma", "Sclerosing Angioma of Lung", "Lung Sclerosing Hemangioma", "Sclerosing Hemangioma, Lung", "Lung Sclerosing Hemangiomas", "Sclerosing Hemangiomas, Lung", "sclerosing hemangioma of lung", "Sclerosing Hemangioma of Lung", "Sclerosing hemangioma of lung", "sclerosing angioma of the lung", "Sclerosing Angioma of the Lung", "Sclerosing haemangioma of lung", "Pulmonary Sclerosing Hemangioma", "pulmonary sclerosing hemangioma", "Pulmonary sclerosing hemangioma", "Sclerosing Hemangioma, Pulmonary", "Pulmonary sclerosing haemangioma", "Pulmonary Sclerosing Hemangiomas", "Sclerosing Hemangiomas, Pulmonary", "Sclerosing Hemangioma of the Lung", "sclerosing hemangioma of the lung", "Hemangioma, Sclerosing, Pulmonary", "Sclerosing hemangioma of lung (disorder)", "Sclerosing pneumocytoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung sclerosing hemangioma", "shortest_name_length": 12}
{"curie": "MONDO:0014670", "names": ["LCCS9", "LETHAL CONGENITAL CONTRACTURE SYNDROME 9", "lethal congenital contracture syndrome 9", "ADGRG6 lethal congenital contracture syndrome", "lethal congenital contracture syndrome type 9", "lethal congenital contracture syndrome caused by mutation in ADGRG6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal congenital contracture syndrome 9", "shortest_name_length": 5}
{"curie": "UMLS:C0160336", "names": ["injury of diaphragm with open wound into cavity", "Injury to Diaphragm with Open Wound into Cavity", "Injury of diaphragm with open wound into cavity", "Injury to diaphragm, with open wound into cavity", "Injury of diaphragm with open wound into cavity (disorder)", "injury of diaphragm with open wound into cavity (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of diaphragm with open wound into cavity", "shortest_name_length": 47}
{"curie": "UMLS:C0278838", "names": ["Prostate cancer recurrent", "Recurrent Prostate Cancer", "cancer prostate recurrent", "recurrent prostate cancer", "prostate cancer recurrent", "prostate cancer, recurrent", "Prostatic cancer recurrent", "Recurrent Prostate Carcinoma", "Recurrent Cancer of Prostate", "Recurrent Cancer of the Prostate", "Carcinoma of the prostate recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate cancer recurrent", "shortest_name_length": 25}
{"curie": "MONDO:0017068", "names": ["upper thoracic spina bifida aperta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "upper thoracic spina bifida aperta", "shortest_name_length": 34}
{"curie": "MONDO:0001409", "names": ["esophagitis", "Esophagitis", "ESOPHAGITIS", "OESOPHAGITIS", "Oesophagitis", "oesophagitis", "Esophagitides", "Esophagitis NOS", "Esophagitis, NOS", "Oesophagitis NOS", "acute esophagitis", "Oesophagitis, NOS", "Acute esophagitis", "Acute Esophagitis", "ESOPHAGITIS, ACUTE", "Acute oesophagitis", "esophagitis (disease)", "Esophagitis (disorder)", "esophagus inflammation", "inflammation; esophagus", "esophagus; inflammation", "esophagitis (diagnosis)", "Esophageal inflammation", "Oesophageal inflammation", "Esophagitis, unspecified", "Oesophagitis, unspecified", "inflammation of esophagus", "Inflammation of esophagus", "Acute esophagitis (disorder)", "Inflammation of the esophagus", "acute esophagitis (diagnosis)", "Inflammation of the oesophagus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophagitis", "shortest_name_length": 11}
{"curie": "MONDO:0003704", "names": ["uterine corpus leiomyomatosis", "body of uterus leiomyomatosis", "leiomyomatosis of body of uterus", "uterine corpus diffuse leiomyomatosis", "Uterine Corpus Diffuse Leiomyomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine corpus diffuse leiomyomatosis", "shortest_name_length": 29}
{"curie": "UMLS:C1709252", "names": ["Non-Neoplastic Pancreatic Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Pancreatic Disorder", "shortest_name_length": 34}
{"curie": "MONDO:0003691", "names": ["Malignant Mesenchymoma", "malignant mesenchymoma", "Childhood Malignant Mesenchymoma", "pediatric malignant mesenchymoma", "childhood malignant mesenchymoma", "malignant mesenchymoma, childhood", "mesenchymoma, malignant, childhood", "malignant mesenchymoma of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood malignant mesenchymoma", "shortest_name_length": 22}
{"curie": "MONDO:0017925", "names": ["T-cell immunodeficiency due to RHOH deficiency", "T-cell immunodeficiency with epidermodysplasia verruciformis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-cell immunodeficiency with epidermodysplasia verruciformis", "shortest_name_length": 46}
{"curie": "MONDO:0012228", "names": ["MYP8", "MYOPIA 8", "Myopia 8", "myopia 8", "MYOPIA 8 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopia 8", "shortest_name_length": 4}
{"curie": "UMLS:C4723619", "names": ["Brain Ependymoma", "Intracranial Ependymoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brain Ependymoma", "shortest_name_length": 16}
{"curie": "MONDO:0015645", "names": ["eating seizures", "eating epilepsy", "Eating epilepsy", "Eating seizures", "eating reflex epilepsy", "Eating reflex epilepsy", "epilepsy reflex eating", "Eating epilepsy (disorder)", "Eating epilepsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eating seizures", "shortest_name_length": 15}
{"curie": "UMLS:C5418793", "names": ["Advanced Pharyngeal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Pharyngeal Carcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0007108", "names": ["anal canal cancer", "Anal Canal Cancer", "Anal Canal Carcinoma", "anal canal carcinoma", "ANAL CANAL CARCINOMA", "cloacogenic carcinoma", "carcinoma of anal canal", "Carcinoma of anal canal", "Carcinoma of the anal canal", "carcinoma of the anal canal", "Carcinoma of anal canal (disorder)", "carcinoma of anal canal (diagnosis)", "anal canal and perianal gland cancer", "Anal Canal and Perianal Gland Cancer", "anal canal and perianal gland carcinoma", "anal canal and Perianal gland carcinoma", "Anal Canal and Perianal Gland Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anal canal carcinoma", "shortest_name_length": 17}
{"curie": "MONDO:0001447", "names": ["Detrussor dyssynergia", "Detrusor sphincter dyssynergia", "detrusor sphincter dyssynergia", "Detrusor and sphincter dyssynergia", "detrusor sphincter dyssynergia (disease)", "DSD - Detrusor and sphincter dyssynergia", "detrusor sphincter dyssynergia (diagnosis)", "Detrusor and sphincter dyssynergia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "detrusor sphincter dyssynergia", "shortest_name_length": 21}
{"curie": "MONDO:0006732", "names": ["drug-Induced dyskinesia", "Drug-Induced Dyskinesia", "drug-induced dyskinesia", "Drug-induced dyskinesia", "drug dyskinesias induced", "Drug-Induced Dyskinesias", "Dyskinesia, Drug-Induced", "Dyskinesia, Drug Induced", "Dyskinesias, Drug-Induced", "Drug-induced dyskinesia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "drug-induced dyskinesia", "shortest_name_length": 23}
{"curie": "MONDO:0000288", "names": ["polycystic echinococcosis", "neotropical echinococcosis", "human polycystic hydatid disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polycystic echinococcosis", "shortest_name_length": 25}
{"curie": "UMLS:C1518187", "names": ["Malignant Lymphoma Follicular, Large Cleaved Cell Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Lymphoma Follicular, Large Cleaved Cell Type", "shortest_name_length": 54}
{"curie": "MONDO:0015944", "names": ["Blastogenesis defect", "blastogenesis defect", "Russell-Weaver-Bull syndrome", "Russell Weaver Bull syndrome", "Axial mesodermal dysplasia spectrum", "axial mesodermal dysplasia spectrum", "Axial mesodermal dysplasia spectrum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "axial mesodermal dysplasia spectrum", "shortest_name_length": 20}
{"curie": "MONDO:0002735", "names": ["Anal Canal Adenocarcinoma", "anal canal adenocarcinoma", "Anal canal adenocarcinoma", "adenocarcinoma of anal canal", "Adenocarcinoma of anal canal", "Adenocarcinoma of Anal Canal", "adenocarcinoma of the anal canal", "Adenocarcinoma of the anal canal", "Adenocarcinoma of the Anal Canal", "anal canal adenocarcinoma (disease)", "adenocarcinoma arising in anal mucosa", "Adenocarcinoma Arising in Anal Mucosa", "Adenocarcinoma of anal canal (disorder)", "adenocarcinoma of anal canal (diagnosis)", "Adenocarcinoma Arising in the Anal Mucosa", "adenocarcinoma arising in the anal mucosa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anal canal adenocarcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0016774", "names": ["LP pigmentosa", "LP pigmentosus", "Lichen planus pigmentosa", "lichen planus pigmentosa", "lichen planus pigmentosus", "Lichen planus pigmentosus", "Lichen planus pigmentosus inversus", "lichen planus pigmentosus inversus", "Lichen planus pigmentosus (disorder)", "Post-inflammatory hyperpigmentation in lichen planus", "Post-inflammatory hyperpigmentation in lichen planus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lichen planus pigmentosus", "shortest_name_length": 13}
{"curie": "MONDO:0002982", "names": ["soft tissue peripheral neuroepithelioma", "Peripheral neuroepithelioma of soft tissue", "Peripheral Neuroepithelioma of Soft Tissues", "peripheral neuroepithelioma of soft tissues", "Peripheral Neuroepithelioma of the Soft Tissues", "peripheral neuroepithelioma of the soft tissues", "peripheral neuroectodermal tumor of soft tissue", "peripheral neuroectodermal tumor of soft tissues", "peripheral Neuroectodermal tumor of soft tissues", "Peripheral Neuroectodermal Tumor of Soft Tissues", "Peripheral Neuroectodermal Tumor of the Soft Tissues", "peripheral neuroectodermal tumor of the soft tissues", "Peripheral primitive neuroectodermal tumor of soft tissue", "Peripheral Primitive Neuroectodermal Tumor of Soft Tissues", "peripheral primitive neuroectodermal tumor of soft tissues", "Peripheral primitive neuroectodermal tumour of soft tissue", "peripheral neuroectodermal tumor of soft tissue (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peripheral primitive neuroectodermal tumor of soft tissues", "shortest_name_length": 39}
{"curie": "MONDO:0016205", "names": ["IRVAN syndrome", "idiopathic retinal-aneurysms-neuroretinitis syndrome", "idiopathic retinal vasculitis-aneurysms-neuroretinitis syndrome", "Idiopathic retinal vasculitis-aneurysms-neuroretinitis syndrome", "Idiopathic retinal vasculitis, aneurysms, neuroretinitis syndrome", "Idiopathic retinal vasculitis, aneurysms and neuroretinitis syndrome", "IRVAN (idiopathic retinal vasculitis, aneurysms, neuroretinitis) syndrome", "Idiopathic retinal vasculitis, aneurysms, neuroretinitis syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IRVAN syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C0280424", "names": ["Adult T-Cell Lymphoma/Leukemia Stage II", "Adult T-cell lymphoma/leukemia stage II", "stage II adult T-cell leukemia/lymphoma", "Stage II Adult T-Cell Lymphoma/Leukemia", "Stage II Adult T-Cell Leukemia/Lymphoma", "Adult T-cell lymphoma/leukaemia stage II", "adult T-cell leukemia/lymphoma, stage II", "Ann Arbor Stage II Adult T-Cell Leukemia/Lymphoma", "HTLV-1 Associated Adult T-Cell Lymphoma/Leukemia Stage II", "Stage II HTLV-1 Associated Adult T-Cell Lymphoma/Leukemia", "stage II HTLV-I associated adult T-cell leukemia/lymphoma", "HTLV-I associated adult T-cell leukemia/lymphoma, stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult T-cell lymphoma/leukemia stage II", "shortest_name_length": 39}
{"curie": "MONDO:0011080", "names": ["Thies Reis syndrome", "Thies-Reis syndrome", "Stapedo-vestibular ankylosis", "Progressive deafness with stapes fixation", "progressive deafness with stapes fixation", "Deafness, Progressive, With Stapes Fixation", "DEAFNESS, PROGRESSIVE, WITH STAPES FIXATION", "deafness, progressive, with stapes fixation", "Progressive hearing loss with stapes fixation", "Progressive deafness with stapes fixation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive deafness with stapes fixation", "shortest_name_length": 19}
{"curie": "MONDO:0013326", "names": ["SLSN7", "Senior-Loken syndrome 7", "SENIOR-Loken syndrome 7", "SENIOR-LOKEN SYNDROME 7", "Senior-Loken syndrome type 7", "SDCCAG8 Senior-Loken syndrome", "Senior-Loken syndrome caused by mutation in SDCCAG8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Senior-Loken syndrome 7", "shortest_name_length": 5}
{"curie": "UMLS:C1336083", "names": ["Squamous Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Squamous Hyperplasia", "shortest_name_length": 20}
{"curie": "MONDO:0018147", "names": ["idiopathic macular telangiectasia type 3", "occlusive idiopathic juxtafoveolar retinal telangiectasis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic macular telangiectasia type 3", "shortest_name_length": 40}
{"curie": "MONDO:0007944", "names": ["TCS1", "MFD1", "Treacher Collins syndrome", "mandibulofacial dysostosis", "TREACHER COLLINS SYNDROME 1", "Treacher Collins syndrome 1", "TREACHER COLLINS syndrome 1", "Treacher-Collins syndrome 1", "TCOF1 Treacher-Collins syndrome", "Treacher Collins syndrome type 1", "Treacher Collins-Franceschetti syndrome", "Treacher-Collins syndrome caused by mutation in TCOF1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Treacher Collins syndrome 1", "shortest_name_length": 4}
{"curie": "MONDO:0004126", "names": ["Thyroiditis", "thyroiditis", "THYROIDITIS", "Thyroiditides", "Thyroiditis NOS", "Thyroiditis, NOS", "thyroiditis (disease)", "Thyroiditis (disorder)", "thyroiditis (diagnosis)", "unspecified thyroiditis", "Thyroiditis, unspecified", "Thyroid gland inflammation", "thyroid gland inflammation", "inflammation of thyroid gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroiditis", "shortest_name_length": 11}
{"curie": "MONDO:0017045", "names": ["Oerter-Friedman-Anderson syndrome", "neuroectodermal-endocrine syndrome", "neuroectodermal endocrine syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuroectodermal-endocrine syndrome", "shortest_name_length": 33}
{"curie": "UMLS:C1262147", "names": ["Scleroderma Renal Crisis", "Scleroderma renal crisis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Scleroderma renal crisis", "shortest_name_length": 24}
{"curie": "MONDO:0017613", "names": ["Medrano Roldan syndrome", "Medrano-Roldan syndrome", "intellectual disability-hypotonia-skin hyperpigmentation syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability-hypotonia-skin hyperpigmentation syndrome", "shortest_name_length": 23}
{"curie": "UMLS:C0276085", "names": ["ecthyma gangrenosum", "Ecthyma gangrenosum", "ecthyma; gangrenosum", "gangrenosum; ecthyma", "Ecthyma gangrenosum (disorder)", "ecthyma gangrenosum was observed", "ecthyma gangrenosum (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ecthyma gangrenosum", "shortest_name_length": 19}
{"curie": "UMLS:C1332062", "names": ["AIDS-Related Vulvovaginal Candidiasis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Vulvovaginal Candidiasis", "shortest_name_length": 37}
{"curie": "UMLS:C1709337", "names": ["Organ Perforation", "Perforation of organ", "Internal Organ Perforation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perforation of organ", "shortest_name_length": 17}
{"curie": "UMLS:C0282644", "names": ["Lethal Acrodysgenital Syndrome", "Lethal Acrodysgenital Syndromes", "Acrodysgenital Syndrome, Lethal", "Syndrome, Lethal Acrodysgenital", "Acrodysgenital Syndromes, Lethal", "Rutledge Friedman Harrod Syndrome", "Smith Lemli Opitz Syndrome, Type 2", "Smith-Lemli-Opitz Syndrome, Type 2", "Smith-Lemli-Opitz Syndrome, Type II", "Smith Lemli Opitz Syndrome, Type II", "Rutledge Lethal Multiple Congenital Anomaly Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Smith-Lemli-Opitz Syndrome, Type II", "shortest_name_length": 30}
{"curie": "MONDO:0012442", "names": ["DFNB66", "autosomal recessive deafness 66", "deafness, autosomal recessive 66", "DEAFNESS, AUTOSOMAL RECESSIVE 66", "Deafness, Autosomal Recessive 66", "deafness, autosomal recessive type 66", "autosomal recessive nonsyndromic deafness 66", "DCDC2 autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 66", "autosomal recessive nonsyndromic deafness type 66", "autosomal recessive nonsyndromic deafness caused by mutation in DCDC2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 66", "shortest_name_length": 6}
{"curie": "MONDO:0054724", "names": ["SPGF20", "spermatogenic failure 20", "SPERMATOGENIC FAILURE 20"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 20", "shortest_name_length": 6}
{"curie": "UMLS:C3897359", "names": ["Thymic Damage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thymic Damage", "shortest_name_length": 13}
{"curie": "MONDO:0007309", "names": ["CMT1A", "HMSN1A", "CMT 1A", "HMSN IA", "HMSN 1A", "Microduplication 17p12", "microduplication 17p12", "Charcot-Marie-Tooth disease Type 1A", "Charcot Marie Tooth disease type 1A", "Charcot-Marie-Tooth Disease Type 1A", "Charcot-Marie-Tooth disease type 1A", "CHARCOT-MARIE-TOOTH DISEASE, TYPE 1A", "Charcot Marie Tooth Disease, Type 1A", "Charcot-Marie-Tooth disease, type 1A", "Charcot-Marie-Tooth Disease, Type 1A", "Charcot-Marie-Tooth disease, type IA", "Charcot Marie Tooth Disease, Type IA", "Charcot-Marie-Tooth syndrome type 1A", "Charcot-Marie-Tooth Disease, Type IA", "Charcot-Marie-Tooth neuropathy type 1A", "Charcot-Marie-Tooth Neuropathy, Type 1A", "Charcot-Marie-Tooth neuropathy, type 1A", "Charcot Marie Tooth Neuropathy, Type 1A", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 1A", "hereditary motor and sensory neuropathy 1A", "Hereditary Motor and Sensory Neuropathy 1A", "Hereditary Motor and Sensory Neuropathy IA", "HEREDITARY MOTOR AND SENSORY NEUROPATHY IA", "Charcot-Marie-Tooth disease Type 1A (diagnosis)", "Charcot-Marie-Tooth disease, type IA (disorder)", "Charcot-Marie-Tooth Disease, Type Ia (disorder)", "CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A", "Charcot-Marie-Tooth Disease, Demyelinating, Type 1A", "Charcot-Marie-Tooth disease, demyelinating, type 1A", "autosomal dominant Charcot-Marie-Tooth disease with focally folded myelin sheaths type 1A", "Charcot-Marie-Tooth disease, autosomal dominant, with focally folded myelin sheaths, type 1A", "Charcot-Marie-Tooth Disease, Autosomal Dominant, With Focally Folded Myelin Sheaths, Type 1A", "CHARCOT-MARIE-TOOTH DISEASE, AUTOSOMAL DOMINANT, WITH FOCALLY FOLDED MYELIN SHEATHS, TYPE 1A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 1A", "shortest_name_length": 5}
{"curie": "MONDO:0011442", "names": ["FASPS1", "advanced sleep phase syndrome 1", "PER2 advanced sleep phase syndrome", "advanced sleep phase syndrome type 1", "familial advanced sleep phase syndrome 1", "advanced sleep phase syndrome, familial, 1", "ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 1", "advanced sleep phase syndrome, familial, type 1", "advanced sleep phase syndrome caused by mutation in PER2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "advanced sleep phase syndrome 1", "shortest_name_length": 6}
{"curie": "UMLS:C0024050", "names": ["lgi bleed", "lower gi bleed", "Lower GI bleeding", "bleeding gi lower", "lower gi bleeding", "Lower GI hemorrhage", "Lower GI haemorrhage", "Intestinal Hemorrhage", "Intestinal hemorrhage", "lower gastrointestinal bleed", "GASTROINTESTINAL BLEED LOWER", "lower gastrointestinal bleeding", "Lower gastrointestinal bleeding", "LOWER GASTROINTESTINAL BLEEDING", "bleeding gastrointestinal lower", "Lower Gastrointestinal Hemorrhage", "Lower gastrointestinal hemorrhage", "Lower gastrointestinal haemorrhage", "Lower GIT - gastrointestinal hemorrhage", "Lower GIT - gastrointestinal haemorrhage", "lower gastrointestinal bleeding (diagnosis)", "Lower gastrointestinal hemorrhage (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lower gastrointestinal hemorrhage", "shortest_name_length": 9}
{"curie": "MONDO:0009605", "names": ["METAG", "CYB5A methemoglobinemia", "methemoglobinemia type 4", "METHEMOGLOBINEMIA TYPE IV", "methemoglobinemia type IV", "Methemoglobinemia Type IV", "methemoglobinemia type IV, formerly", "METHEMOGLOBINEMIA TYPE IV, FORMERLY", "pure isolated 17,20-lyase deficiency", "ISOLATED 17,20-LYASE DEFICIENCY, PURE", "isolated 17,20-lyase deficiency, Pure", "METHEMOGLOBINEMIA AND AMBIGUOUS GENITALIA", "methemoglobinemia and ambiguous genitalia", "methemoglobinemia caused by mutation in CYB5A", "Methemoglobinemia due to Deficiency of Cytochrome B5", "methemoglobinemia due to deficiency of cytochrome b5", "methemoglobinemia due to deficiency of cytochrome B5", "METHEMOGLOBINEMIA DUE TO DEFICIENCY OF CYTOCHROME b5, FORMERLY", "methemoglobinemia due to deficiency of cytochrome B5, formerly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "methemoglobinemia type 4", "shortest_name_length": 5}
{"curie": "UMLS:C0278470", "names": ["stage I adult HD", "adult HD, stage I", "HD, stage I, adult", "HD, adult, stage I", "Stage I Hodgkin Lymphoma", "stage I adult Hodgkin lymphoma", "Stage I Adult Hodgkin Lymphoma", "Stage I Adult Hodgkin's Disease", "Adult Hodgkin's Disease Stage I", "stage I adult Hodgkin's disease", "Adult Hodgkin's Lymphoma Stage I", "adult Hodgkin's disease, stage I", "Stage I Adult Hodgkin's Lymphoma", "Hodgkin's disease, stage I, adult", "lymphoma, stage I adult Hodgkin's", "Hodgkin's lymphoma, stage I, adult", "Ann Arbor Stage I Adult Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Adult Hodgkin Lymphoma", "shortest_name_length": 16}
{"curie": "MONDO:0001776", "names": ["prostate stone", "Prostatic Stone", "prostate stones", "Prostatic stone", "prostatic stone", "Prostate stones", "prostatic stones", "prostate calculus", "Stone of Prostate", "Calculus;prostate", "Stone of prostate", "Prostate Calculus", "prostate; calculus", "PROSTATE, CALCULUS", "Calculus prostatic", "calculus; prostate", "PROSTATIC CALCULUS", "prostatic calculus", "Prostatic calculus", "prostatic lithiasis", "Prostatic lithiasis", "Calculus of prostate", "calculus of prostate", "Calculus of prostate (disorder)", "calculus of prostate (diagnosis)", "prostate gland lower urinary tract calculus", "lower urinary tract calculus of prostate gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate calculus", "shortest_name_length": 14}
{"curie": "MONDO:0006828", "names": ["midline granuloma", "granuloma; midline", "GRANULOMA, MIDLINE", "midline; granuloma", "granuloma lethal midline", "Lethal Midline Granuloma", "lethal midline granuloma", "Lethal midline granuloma", "Lethal Midline Granulomas", "Midline Granuloma, Lethal", "Granuloma, Lethal Midline", "Lethal midline reticulosis", "lethal midline reticulosis", "Granulomas, Lethal Midline", "Midline Granulomas, Lethal", "Malignant granuloma of face", "malignant granuloma of face", "Idiopathic midline granuloma", "midfacial Necrotising lesion", "Midfacial Necrotising Lesion", "GRANULOMA, IDIOPATHIC MIDLINE", "Lethal midline granuloma of face", "Lethal midline granuloma (disorder)", "lethal midline granuloma (diagnosis)", "nasal cavity and paranasal sinus midline lethal granuloma", "nasal cavity and paranasal sinus lethal midline granuloma", "nasal cavity and paranasal sinus lethal Midline granuloma", "paranasal sinus and nasal cavity midline lethal granuloma", "Nasal Cavity and Paranasal Sinus Lethal Midline Granuloma", "midline lethal granuloma, paranasal sinus and nasal cavity", "Midline lethal granuloma of nasal cavity and paranasal sinus", "Midline Lethal Granuloma of Nasal Cavity and Paranasal Sinus", "Midline lethal granuloma of the nasal cavity and paranasal sinus", "Midline Lethal Granuloma of the Nasal Cavity and Paranasal Sinus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasal cavity and paranasal sinus lethal midline granuloma", "shortest_name_length": 17}
{"curie": "MONDO:0006217", "names": ["GBASC", "Gallbladder Adenosquamous Cancer", "gallbladder adenosquamous cancer", "Gallbladder Adenosquamous Carcinoma", "gallbladder adenosquamous carcinoma", "Gallbladder adenosquamous carcinoma", "adenosquamous gallbladder carcinoma", "gall bladder adenosquamous carcinoma", "Adenosquamous Carcinoma of Gallbladder", "adenosquamous carcinoma of gallbladder", "adenosquamous carcinoma of the gallbladder", "Adenosquamous Carcinoma of the Gallbladder", "Adenosquamous carcinoma of the gallbladder", "adenosquamous carcinoma of gallbladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gallbladder adenosquamous carcinoma", "shortest_name_length": 5}
{"curie": "UMLS:C0271092", "names": ["Cone dystrophy", "Progressive cone dystrophy", "Progressive cone dystrophy (without rod involvement)", "Progressive cone dystrophy (without rod involvement) (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Progressive cone dystrophy (without rod involvement)", "shortest_name_length": 14}
{"curie": "MONDO:0000004", "names": ["Hypoadrenalism", "hypoadrenalism", "Adrenal failure", "adrenal failure", "Hypocortisolism", "hypocortisolism", "hypocortisolemia", "Hypocortisolemia", "hypoadrenocorticism", "Hypoadrenocorticism", "HYPOFUNCTION ADRENAL", "ADRENAL HYPOFUNCTION", "Hypofunction adrenal", "adrenal hypofunction", "Adrenal hypofunction", "INSUFFICIENCY ADRENAL", "Adrenal Insufficiency", "adrenal insufficiency", "Insufficiency adrenal", "Insufficiency;adrenal", "adrenal hypofunctions", "insufficiency adrenal", "Adrenal insufficiency", "ADRENAL INSUFFICIENCY", "insufficiency; adrenal", "adrenal; insufficiency", "Adrenal Insufficiencies", "adrenal insufficiencies", "Hypoadrenocorticism, NOS", "Hypoadrenalism (disorder)", "Adrenal insufficiency NOS", "Adrenal insufficiency, NOS", "ADRENAL CORTEX INSUFFIENCY", "Adrenal Gland Hypofunction", "deficiency; corticoadrenal", "Adrenal gland hypofunction", "adrenal cortex; deficiency", "corticoadrenal; deficiency", "Hypofunction, Adrenal Gland", "adrenocortical hypofunction", "Adrenocortical hypofunction", "ADRENAL CORTEX HYPOFUNCTION", "adrenal gland insufficiency", "Adrenal cortex hypofunction", "Adrenal Gland Insufficiency", "Adrenal gland insufficiency", "Adrenal cortex insufficiency", "corticoadrenal; hypofunction", "hypofunction; adrenocortical", "corticoadrenal insufficiency", "Corticoadrenal insufficiency", "Insufficiency adrenal cortex", "INSUFFICIENCY ADRENAL CORTEX", "Adrenocortical Insufficiency", "adrenal cortex insufficiency", "adrenocortical insufficiency", "Adrenocortical insufficiency", "adrenal cortical hypofunction", "Adrenal cortical hypofunction", "Adrenal Cortical Hypofunction", "adrenal cortical insufficiency", "ADRENAL INSUFFICIENCY CORTICAL", "Adrenal Cortical Insufficiency", "Adrenal cortical hypofunctions", "ADRENAL CORTICAL INSUFFICIENCY", "Adrenal cortical insufficiency", "Adrenocortical hypofunction, NOS", "Corticoadrenal insufficiency NOS", "adrenal insufficiency (diagnosis)", "Corticoadrenal insufficiency, NOS", "Adrenal cortical hypofunction, NOS", "Adrenocortical insufficiency syndrome", "Adrenal cortical hypofunction (disorder)", "corticoadrenal insufficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adrenocortical insufficiency", "shortest_name_length": 14}
{"curie": "UMLS:C0232841", "names": ["bladder dysfunction", "Bladder dysfunction", "dysfunction; bladder", "bladder dysfunctions", "Bladder dysfunction, NOS", "Bladder dysfunction (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder dysfunction", "shortest_name_length": 19}
{"curie": "MONDO:0009112", "names": ["Rcdp2", "RCDP2", "GNPAT DEFICIENCY", "Gnpat Deficiency", "Gnpat deficiency", "GNPAT deficiency", "Dhapat deficiency", "DHAPAT deficiency", "DHAPAT DEFICIENCY", "Dhapat Deficiency", "GNPAT rhizomelic chondrodysplasia punctata", "type 2 rhizomelic chondrodysplasia punctata", "Rhizomelic chondrodysplasia punctata type 2", "Type 2 rhizomelic chondrodysplasia punctata", "rhizomelic chondrodysplasia punctata type 2", "RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 2", "Rhizomelic chondrodysplasia punctata, type 2", "rhizomelic chondrodysplasia punctata, type 2", "Glyceronephosphate acyltransferase deficiency", "Glyceronephosphate O-Acyltransferase Deficiency", "GLYCERONEPHOSPHATE O-ACYLTRANSFERASE DEFICIENCY", "Glyceronephosphate O-acyltransferase deficiency", "DIHYDROXYACETONEPHOSPHATE ACYLTRANSFERASE DEFICIENCY", "Dihydroxyacetonephosphate Acyltransferase Deficiency", "Dihydroxyacetonephosphate acyltransferase deficiency", "Rhizomelic chondrodysplasia punctata type 2 (disorder)", "rhizomelic chondrodysplasia punctata type 2 (diagnosis)", "Human dihydroxyacetonephosphate acyltransferase deficiency", "Chondrodysplasia punctata, rhizomelic, due to DHAPAT deficiency", "rhizomelic chondrodysplasia punctata caused by mutation in GNPAT", "peroxisomal dihydroxyacetonephosphate acyltransferase deficiency", "Peroxisomal dihydroxyacetonephosphate acyltransferase deficiency", "PEROXISOMAL DIHYDROXYACETONEPHOSPHATE ACYLTRANSFERASE DEFICIENCY", "Peroxisomal Dihydroxyacetonephosphate Acyltransferase Deficiency", "chondrodysplasia punctata, rhizomelic, due to dihydroxyacetonephosphate", "chondrodysplasia punctata, rhizomelic, due to Dihydroxyacetonephosphate acyltransferase deficiency", "Chondrodysplasia Punctata, Rhizomelic, Due To Dihydroxyacetonephosphate Acyltransferase Deficiency", "CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC, DUE TO DIHYDROXYACETONEPHOSPHATE ACYLTRANSFERASE DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rhizomelic chondrodysplasia punctata type 2", "shortest_name_length": 5}
{"curie": "MONDO:0010181", "names": ["oculogastrointestinal muscular dystrophy", "Oculogastrointestinal muscular dystrophy", "Oculogastrointestinal Muscular Dystrophy", "Muscular dystrophy, oculogastrointestinal", "MUSCULAR DYSTROPHY, OCULOGASTROINTESTINAL", "muscular dystrophy, oculogastrointestinal", "Visceral myopathy familial external ophthalmoplegia", "Oculogastrointestinal muscular dystrophy (disorder)", "visceral myopathy - familial external ophthalmoplegia", "familial visceral myopathy with external ophthalmoplegia", "INTESTINAL PSEUDOOBSTRUCTION WITH EXTERNAL OPHTHALMOPLEGIA", "Visceral Myopathy, Familial, With External Ophthalmoplegia", "intestinal pseudoobstruction with external ophthalmoplegia", "visceral myopathy, familial, with external ophthalmoplegia", "Intestinal pseudoobstruction with external ophthalmoplegia", "VISCERAL MYOPATHY, FAMILIAL, WITH EXTERNAL OPHTHALMOPLEGIA", "visceral myopathy-familial external ophthalmoplegia syndrome", "Visceral myopathy-familial external ophthalmoplegia syndrome", "Visceral myopathy with familial external ophthalmoplegia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculogastrointestinal muscular dystrophy", "shortest_name_length": 40}
{"curie": "MONDO:0019555", "names": ["panniculitis and localized lipodystrophy", "panniculitis-induced localized lipodystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "panniculitis and localized lipodystrophy", "shortest_name_length": 40}
{"curie": "MONDO:0002546", "names": ["SCHW", "Neurinoma", "neurinoma", "schwannoma", "SCHWANNOMA", "neurinomas", "Schwannoma", "Neurinomas", "Schwannomas", "neurilemoma", "Neurilemoma", "schwannomas", "Neurolemmoma", "neurilemmoma", "Neurilemmoma", "neurolemmoma", "Neurilemomas", "Neurilemmomas", "neurilemmomas", "Neurilemoma NOS", "Schwannoma, NOS", "Neurilemmoma NOS", "Benign schwannoma", "Neurilemmoma, NOS", "Benign Schwannoma", "Schwannoma benign", "benign schwannoma", "ancient schwannoma", "Neurilemoma benign", "Schwann cell tumor", "schwannoma, benign", "SCHWANNOMA, BENIGN", "Schwann cell tumour", "benign neurilemmoma", "Benign Neurilemmoma", "Neurilemmoma benign", "Schwannoma (disorder)", "schwannoma (diagnosis)", "psammomatous schwannoma", "Psammomatous schwannoma", "Schwannoma (WHO Grade I)", "schwannoma (WHO grade I)", "Schwannoma (Who Grade I)", "Peripheral fibroblastoma", "peripheral fibroblastoma", "Schwannoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schwannoma", "shortest_name_length": 4}
{"curie": "UMLS:C1336099", "names": ["Stage 0 Urethra Cancer", "Urethra Cancer Stage 0", "Stage 0 Urethral Cancer", "Stage 0 Urethra Carcinoma", "Stage 0 Urethral Carcinoma", "Stage 0 Carcinoma of Urethra", "Stage 0 Urethral Cancer AJCC v7", "Stage 0 Carcinoma of the Urethra", "stage 0 urethral carcinoma in situ"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Urethral Cancer AJCC v7", "shortest_name_length": 22}
{"curie": "MONDO:0029000", "names": ["TOX", "toxic", "toxics", "toxicity", "Toxicity", "Toxicosis", "toxicosis", "Poisoning", "poisoning", "toxicities", "poisonings", "Poisonings", "POISONINGS", "Toxic effect", "intoxication", "by poisoning", "toxic effect", "Poisoning by", "poisoning by", "Poisoning NOS", "effects toxics", "Toxicosis, NOS", "Poisoning, NOS", "Toxic effect of", "poisoning syndrome", "Poisoning syndrome", "Poisoning Syndromes", "Poisoning (disorder)", "poisoning (diagnosis)", "Poisoning syndrome, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "poisoning", "shortest_name_length": 3}
{"curie": "MONDO:0010528", "names": ["Anosmia", "ANOSMIA", "anosmia", "anosmias", "smell loss", "SMELL LOSS", "loss smell", "Smell loss", "Lost smell", "Smell Loss", "sense smell", "anosphrasia", "smell; loss", "loss; smell", "smell sense", "Absent smell", "Loss of smell", "Loss of Smell", "Smell, absent", "loss of smell", "smell disorder", "Smell Disorder", "smell disorders", "disorder; smell", "Smell disorders", "smell; disorder", "Smell Disorders", "Loss (of);smell", "loss sense smell", "no sense of smell", "Disorder of smell", "disorder smelling", "No sense of smell", "anosmia (disease)", "disorders smelling", "Smelling Disorders", "Olfaction Disorder", "anosmia as symptom", "of smell disorders", "olfaction disorder", "anosmia (diagnosis)", "Lost sense of smell", "sense of smell lost", "Sense of smell lost", "Olfaction Disorders", "lost sense of smell", "Sense of smell absent", "Absent sense of smell", "Loss of sense of smell", "Sense of smell, absent", "loss of sense of smell", "Loss of the sense of smell", "Disorder of smell (disorder)", "sense of smell lost (anosmia)", "loss; smell, complete (anosmia)", "smell; loss, complete (anosmia)", "Loss of sense of smell (finding)", "loss of sense of smell (symptom)", "Anosmia (loss of sense of smell)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anosmia", "shortest_name_length": 7}
{"curie": "MONDO:0032598", "names": ["DEE68", "EIEE68", "early infantile epileptic encephalopathy 68", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 68", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 68", "epileptic encephalopathy, early infantile, 68", "developmental and epileptic encephalopathy 68", "developmental and epileptic encephalopathy, 68"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 68", "shortest_name_length": 5}
{"curie": "MONDO:0035161", "names": ["progressive dementia with neuroserpin inclusion bodies", "late-onset familial encephalopathy with neuroserpin inclusion bodies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive dementia with neuroserpin inclusion bodies", "shortest_name_length": 54}
{"curie": "UMLS:C3852986", "names": ["Nonocclusive Mesenteric Ischemia", "Mesenteric Ischemia, Nonocclusive", "Nonocclusive Mesenteric Ischemias", "Ischemia, Nonocclusive Mesenteric", "Mesenteric Ischemias, Nonocclusive", "Ischemias, Nonocclusive Mesenteric"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nonocclusive Mesenteric Ischemia", "shortest_name_length": 32}
{"curie": "MONDO:0016482", "names": ["UPD(11)mat", "silver-Russell syndrome due to maternal uniparental disomy of chromosome 11", "Silver-Russell syndrome due to maternal uniparental disomy of chromosome type 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "silver-Russell syndrome due to maternal uniparental disomy of chromosome 11", "shortest_name_length": 10}
{"curie": "MONDO:0021932", "names": ["Gambian Trypanosomiasis", "Gambian trypanosomiasis", "trypanosomiasis; Gambian", "Gambian; trypanosomiasis", "Trypanosomiasis, Gambian", "Gambiense trypanosomiasis", "Chronic sleeping sickness", "chronic sleeping sickness", "Gambian sleeping sickness", "West African; trypanosomiasis", "trypanosomiasis; West African", "West African sleeping sickness", "trypanosomiasis; African, West", "African; trypanosomiasis, West", "West African; sleeping sickness", "sleeping sickness; West African", "Gambian African sleeping sickness", "infection by Trypanosoma gambiense", "Infection by Trypanosoma gambiense", "Gambiense trypanosomiasis infection", "Trypanosoma brucei gambiense; infection", "infection; Trypanosoma brucei gambiense", "Infection caused by Trypanosoma gambiense", "Gambian African sleeping sickness (diagnosis)", "trypanosomiasis; Trypanosoma brucei gambiense", "trypanosomiasis African sleeping sickness Gambian", "Infection caused by Trypanosoma gambiense (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infection by Trypanosoma gambiense", "shortest_name_length": 23}
{"curie": "MONDO:0024620", "names": ["Polio virus meningitis", "polio virus meningitis", "meningitis caused by poliovirus", "Meningitis caused by Human poliovirus", "meningitis caused by human poliovirus", "Meningitis caused by Human poliovirus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "meningitis caused by poliovirus", "shortest_name_length": 22}
{"curie": "UMLS:C0920673", "names": ["virus related cancer", "Virus-Related Cancer", "Virus Related Cancer", "Virus Related Malignancy", "Virus-Related Malignancy", "Virus-Related Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Virus-Related Malignant Neoplasm", "shortest_name_length": 20}
{"curie": "MONDO:0011480", "names": ["DFNA26", "DFNA20", "autosomal dominant deafness 20", "DEAFNESS, AUTOSOMAL DOMINANT 20", "deafness, autosomal dominant 20", "Deafness, Autosomal Dominant 20", "deafness, autosomal dominant 20/26", "deafness, autosomal dominant type 20", "autosomal dominant nonsyndromic deafness 20", "ACTG1 autosomal dominant nonsyndromic deafness", "autosomal dominant nonsyndromic hearing loss 20", "autosomal dominant nonsyndromic deafness type 20", "autosomal dominant nonsyndromic deafness caused by mutation in ACTG1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 20", "shortest_name_length": 6}
{"curie": "UMLS:C1335718", "names": ["Relapsed Mouth Carcinoma", "Recurrent Mouth Carcinoma", "Relapsed Oral Cavity Cancer", "Relapsed Carcinoma of Mouth", "Recurrent Carcinoma of Mouth", "Recurrent Oral Cavity Cancer", "Relapsed Oral Cavity Carcinoma", "Relapsed Carcinoma of the Mouth", "Recurrent Oral Cavity Carcinoma", "Recurrent Carcinoma of the Mouth", "Relapsed Carcinoma of Oral Cavity", "Recurrent Carcinoma of Oral Cavity", "Relapsed Carcinoma of the Oral Cavity", "Recurrent Carcinoma of the Oral Cavity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Oral Cavity Carcinoma", "shortest_name_length": 24}
{"curie": "UMLS:C3280743", "names": ["JSLE", "CSLE", "PSLE", "Juvenile SLE", "Pediatric SLE", "Childhood-Onset Systemic Lupus Erythematosus", "Systemic lupus erythematosus, childhood onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Systemic lupus erythematosus, childhood onset", "shortest_name_length": 4}
{"curie": "MONDO:0034212", "names": ["methotrexate toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "methotrexate toxicity", "shortest_name_length": 21}
{"curie": "UMLS:C1141861", "names": ["Procedural complication", "Periprocedural complication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Procedural complication", "shortest_name_length": 23}
{"curie": "MONDO:0000996", "names": ["Prostate Lymphoma", "prostate lymphoma", "lymphoma of prostate", "Lymphoma of Prostate", "prostate gland lymphoma", "lymphoma of the prostate", "Lymphoma of the Prostate", "Primary Prostate Lymphoma", "primary prostate lymphoma", "lymphoma of prostate gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate lymphoma", "shortest_name_length": 17}
{"curie": "MONDO:0017244", "names": ["Pseudoxanthomatous DCM", "infiltrative small vesicular DCM", "pseudoxanthomatous diffuse cutaneous mastocytosis", "infiltrative small vesicular diffuse cutaneous mastocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudoxanthomatous diffuse cutaneous mastocytosis", "shortest_name_length": 22}
{"curie": "MONDO:0019394", "names": ["Boichis disease", "Boichis syndrome", "Senior-Boichis syndrome", "nephronophthisis-hepatic fibrosis syndrome", "Nephronophthisis hepatic fibrosis syndrome", "Nephronophthisis-hepatic fibrosis syndrome", "Nephronophthisis hepatic fibrosis syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Senior-Boichis syndrome", "shortest_name_length": 15}
{"curie": "UMLS:C0151995", "names": ["Degenerated Uterine Fibroid", "Fibroid uterine degenerated", "FIBROID UTERINE DEGENERATED", "Uterine Fibroid Degenerated", "UTERINE FIBROIDS DEGENERATED", "Uterine fibroids degenerated", "Leiomyoma uterine degenerated", "LEIOMYOMA UTERINE DEGENERATED", "Uterine Leiomyoma Degenerated", "Uterine leiomyoma degeneration", "Degeneration of uterine fibroid", "DEGENERATION OF UTERINE FIBROID", "Degeneration of uterine leiomyoma", "Uterine Corpus Degenerated Leiomyoma", "Degeneration of uterine fibroid (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Degeneration of uterine fibroid", "shortest_name_length": 27}
{"curie": "UMLS:C1880790", "names": ["Flexural Skin Nevus", "Nevus of Flexural Skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Flexural Skin Nevus", "shortest_name_length": 19}
{"curie": "MONDO:0020505", "names": ["ravine syndrome", "Ravine syndrome", "RAVINE syndrome", "progressive encephalopathy with severe infantile anorexia", "Progressive encephalopathy with severe infantile anorexia", "Progressive encephalopathy with severe infantile anorexia (disorder)", "Reunion island-anorexia-vomiting which is irrepressible-neurological signs syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ravine syndrome", "shortest_name_length": 15}
{"curie": "UMLS:C4764280", "names": ["Unresectable Renal Pelvis Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Renal Pelvis Urothelial Carcinoma", "shortest_name_length": 46}
{"curie": "UMLS:C1112213", "names": ["cholestasis neonatal", "neonatal cholestasis", "Neonatal cholestasis", "Cholestasis, neonatal", "Cholestasis in newborn", "cholestasis in newborn", "Cholestasis in newborn (disorder)", "cholestasis in newborn (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cholestasis in newborn", "shortest_name_length": 20}
{"curie": "UMLS:C5236144", "names": ["Sporadic Malignant Peripheral Nerve Sheath Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sporadic Malignant Peripheral Nerve Sheath Tumor", "shortest_name_length": 48}
{"curie": "MONDO:0009465", "names": ["FIPA", "MINAT", "GIDID", "GIDID1", "CID-MIA/early-onset IBD", "Multiple intestinal atresia", "intestinal atresia multiple", "multiple intestinal atresia", "intestinal atresia, multiple", "Intestinal Atresia, Multiple", "INTESTINAL ATRESIA, MULTIPLE", "multiple gastrointestinal atresias", "Multiple gastrointestinal atresias", "Hereditary multiple enteric atresia", "Hereditary multiple intestinal atresia", "Familial intestinal polyatresia syndrome", "FAMILIAL INTESTINAL POLYATRESIA SYNDROME", "familial intestinal polyatresia syndrome", "Familial Intestinal Polyatresia Syndrome", "Familial multiple-level intestinal atresia", "Multiple gastrointestinal atresias (disorder)", "combined immunodeficiency-enteropathy spectrum", "FIPA - Familial intestinal polyatresia syndrome", "gastrointestinal defects and immunodeficiency syndrome", "GASTROINTESTINAL DEFECTS AND IMMUNODEFICIENCY SYNDROME 1", "MULTIPLE INTESTINAL ATRESIA AND/OR INFLAMMATORY BOWEL DISEASE WITH OR WITHOUT IMMUNODEFICIENCY", "intestinal atresia, multiple and/or inflammatory bowel disease with or without immunodeficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple intestinal atresia", "shortest_name_length": 4}
{"curie": "OMIM:270900", "names": ["SPASTIC PSEUDOSCLEROSIS", "Spastic Pseudosclerosis", "spastic pseudosclerosis", "CORTICOPALLIDODEGENERATION", "Corticopallidodegeneration", "Disseminated Encephalomyelopathy", "DISSEMINATED ENCEPHALOMYELOPATHY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 23}
{"curie": "MONDO:0006283", "names": ["Lung Lymphoepithelial Carcinoma", "Lymphoepithelioma-Like Lung Carcinoma", "Lung Lymphoepithelioma-Like Carcinoma", "lymphoepithelioma-like lung carcinoma", "lymphoepithelioma-like carcinoma of the lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphoepithelioma-like lung carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0004439", "names": ["periocular meningioma", "Periocular Meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "periocular meningioma", "shortest_name_length": 21}
{"curie": "MONDO:0030729", "names": ["TEVANED1", "TEBIVANED1", "Tessadori-van Haaften neurodevelopmental syndrome 1", "TESSADORI-BICKNELL-VAN HAAFTEN NEURODEVELOPMENTAL SYNDROME 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tessadori-van Haaften neurodevelopmental syndrome 1", "shortest_name_length": 8}
{"curie": "UMLS:C0854706", "names": ["infection neonate", "Neonatal infection", "infection; newborn", "neonatal infection", "infection neonatal", "infection neonates", "infections neonate", "newborn; infection", "Neonatal infections", "infections neonatal", "infections neonates", "Neonatal infection NOS", "Infection of newborn NOS", "Infection in the neonate", "infection in the neonate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neonatal infection", "shortest_name_length": 17}
{"curie": "UMLS:C5206676", "names": ["Head and Neck CUP", "Head and Neck Carcinoma of Unknown Primary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Head and Neck Carcinoma of Unknown Primary", "shortest_name_length": 17}
{"curie": "MONDO:0003005", "names": ["Macular Edema", "edema macular", "macular edema", "Macular edema", "MACULAR EDEMA", "macular oedema", "edema, macular", "Edema, Macular", "Macular oedema", "MACULAR OEDEMA", "Macular retinal edema", "macular retinal edema", "macular retinal oedema", "Retinal edema, macular", "Macular retinal oedema", "macula lutea retinal edema", "retinal edema of macula lutea", "Macular retinal edema (disorder)", "macular retinal edema (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macular retinal edema", "shortest_name_length": 13}
{"curie": "UMLS:C0750968", "names": ["CNS Metabolic Disorder", "Metabolic Disorder, CNS", "CNS Metabolic Disorders", "Metabolic Disorders, CNS", "Central Nervous System Metabolic Disorders", "Metabolic Disorders, Central Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Metabolic Disorders", "shortest_name_length": 22}
{"curie": "MONDO:0007720", "names": ["Double inguinal hernia", "double inguinal hernia", "inguinal double hernia", "Hernia, Double Inguinal", "HERNIA, DOUBLE INGUINAL", "hernia, double inguinal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hernia, double inguinal", "shortest_name_length": 22}
{"curie": "MONDO:0006486", "names": ["UVM", "uvea melanoma", "iris melanoma", "Iris melanoma", "uveal melanoma", "Uveal melanoma", "Uveal Melanoma", "melanoma, uveal", "Melanoma, Uveal", "MELANOMA, UVEAL", "Melanoma of uvea", "melanoma of Uvea", "melanoma of uvea", "Melanoma of Uvea", "Choroidal melanoma", "choroidal melanoma", "Intraocular Melanoma", "Melanoma of the Uvea", "Intraocular melanoma", "intraocular melanoma", "Uveal Tract Melanoma", "melanoma of the uvea", "melanoma, intraocular", "uvea melanoma (disease)", "Intraocular melanoma NOS", "melanoma, uveal, malignant", "melanoma (disease) of uvea", "MELANOMA, UVEAL, MALIGNANT", "Melanoma of uvea (disorder)", "Eye cancer, intraocular melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uveal melanoma", "shortest_name_length": 3}
{"curie": "MONDO:0016921", "names": ["Duplication of chromosome 1", "partial trisomy of chromosome 1", "Partial trisomy of chromosome 1", "partial duplication of chromosome 1", "Partial duplication of chromosome 1", "partial duplication of chromosome type 1", "Partial trisomy of chromosome 1 (disorder)", "Partial trisomy of chromosome 1 (diagnosis)", "anomaly of chromosome pair partial trisomy chromosome 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of chromosome 1", "shortest_name_length": 27}
{"curie": "UMLS:C5205963", "names": ["Seminal Vesicle Mixed Epithelial and Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Seminal Vesicle Mixed Epithelial and Stromal Tumor", "shortest_name_length": 50}
{"curie": "MONDO:0044690", "names": ["OPN", "Optic perineuritis", "optic perineuritis", "Optic perineuritis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "optic perineuritis", "shortest_name_length": 3}
{"curie": "UMLS:C0751924", "names": ["Sciatic Nerve Neuralgia-Neuritis", "Neuralgia-Neuritis, Sciatic Nerve", "Neuralgia Neuritis, Sciatic Nerve", "Sciatic Nerve Neuralgia-Neuritides", "Neuralgia-Neuritides, Sciatic Nerve"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neuralgia-Neuritis, Sciatic Nerve", "shortest_name_length": 32}
{"curie": "MONDO:0010926", "names": ["HHC3", "FBH3", "FBHOk", "FHH type 3", "hpocalciuric hypercalcemia, type III", "hypocalciuric hypercalcemia type III", "familial benign hypercalcemia, type 3", "Familial benign hypercalcemia, type 3", "Hypercalcemia, familial benign, type 3", "familial hypocalciuric hypercalcemia 3", "hypercalcemia, familial benign, type 3", "FAMILIAL BENIGN HYPERCALCEMIA, TYPE III", "Familial Benign Hypercalcemia, Type III", "Hypercalcemia, Familial Benign, Type III", "HYPERCALCEMIA, FAMILIAL BENIGN, TYPE III", "AP2S1 familial hypocalciuric hypercalcemia", "familial hypocalciuric hypercalcemia type 3", "Familial hypocalciuric hypercalcemia type 3", "HYPERCALCEMIA, FAMILIAL BENIGN, OKLAHOMA TYPE", "familial hypocalciuric hypercalcemia type III", "hypercalcemia, familial benign, Oklahoma type", "Hypercalcemia, familial benign, Oklahoma type", "Hypocalciuric hypercalcemia, familial, type 3", "hypocalciuric hypercalcemia, familial, type 3", "familial benign hypercalcemia, Oklahoma variant", "HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III", "hypocalciuric hypercalcemia, familial, type III", "Hypocalciuric Hypercalcemia, Familial, Type III", "Familial benign hypercalcemia, Oklahoma variant", "familial hypocalciuric hypercalcemia type III (diagnosis)", "familial hypocalciuric hypercalcemia caused by mutation in AP2S1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial hypocalciuric hypercalcemia 3", "shortest_name_length": 4}
{"curie": "MONDO:0013852", "names": ["CMH21", "hypertrophic cardiomyopathy 21", "cardiomyopathy, hypertrophic, 21", "hypertrophic cardiomyopathy type 21", "cardiomyopathy familial hypertrophic 21", "CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 21", "cardiomyopathy, familial hypertrophic, 21"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophic cardiomyopathy 21", "shortest_name_length": 5}
{"curie": "MONDO:0011853", "names": ["CCSPD", "camptosynpolydactyly, complex", "Camptosynpolydactyly, Complex", "CAMPTOSYNPOLYDACTYLY, COMPLEX", "Camptosynpolydactyly, complex", "camptopolydactyly, disorganization type", "Camptopolydactyly, Disorganization Type", "CAMPTOPOLYDACTYLY, DISORGANIZATION TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Camptosynpolydactyly, complex", "shortest_name_length": 5}
{"curie": "MONDO:0024430", "names": ["dyschiria", "allochiria", "Dyschirias", "Allesthesia", "allesthesia", "Alloesthesia", "Allesthesias", "Alloesthesias", "Allachesthesia", "Allachesthesias", "false allochiria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "allesthesia", "shortest_name_length": 9}
{"curie": "EFO:0004826", "names": ["anti-neutrophil antibody associated vasculitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anti-neutrophil antibody associated vasculitis", "shortest_name_length": 46}
{"curie": "MONDO:0007672", "names": ["GVM", "VMGLOM", "Glomangiomatosis", "glomangiomatosis", "Familial Glomangioma", "familial glomangioma", "Glomus vagale tumors", "Glomangiomas, Multiple", "hereditary glomangioma", "glomangiomas, multiple", "Multiple glomus tumors", "GLOMANGIOMAS, MULTIPLE", "Hereditary Glomangioma", "multiple glomus tumors", "glomus tumors, multiple", "Glomus Tumors, Multiple", "GLOMUS TUMORS, MULTIPLE", "glomuvenous malformation", "Glomuvenous malformation", "Glomuvenous malformations", "GLOMUVENOUS malformations", "GLOMUVENOUS MALFORMATIONS", "Hereditary multiple glomangioma", "Hereditary multiple glomangiomas", "hereditary multiple glomangiomas", "Glomuvenous malformation (disorder)", "Venous Malformations With Glomus Cells", "Venous malformations with glomus cells", "VENOUS MALFORMATIONS WITH GLOMUS CELLS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glomuvenous malformation", "shortest_name_length": 3}
{"curie": "UMLS:C0333883", "names": ["Severe Glandular Cell Atypia", "Severe glandular cell atypia", "Severe glandular cell atypia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Severe glandular cell atypia", "shortest_name_length": 28}
{"curie": "UMLS:C0877048", "names": ["Oral fungal infection", "oral fungal infection", "fungal infections oral", "Oral fungal infection NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral fungal infection", "shortest_name_length": 21}
{"curie": "MONDO:0021073", "names": ["paraneoplastic syndrome", "PARANEOPLASTIC SYNDROME", "Paraneoplastic syndrome", "Paraneoplastic Syndrome", "Paraneoplastic syndromes", "Paraneoplastic Syndromes", "paraneoplastic syndromes", "Syndrome, Paraneoplastic", "Syndromes, Paraneoplastic", "Paraneoplastic syndrome (disorder)", "paraneoplastic syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paraneoplastic syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0016260", "names": ["uterine corpus rhabdomyosarcoma", "Uterine Corpus Rhabdomyosarcoma", "body of uterus rhabdomyosarcoma", "rhabdomyosarcoma of the corpus uteri", "body of uterus rhabdomyosarcoma (disease)", "rhabdomyosarcoma (disease) of body of uterus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine corpus rhabdomyosarcoma", "shortest_name_length": 31}
{"curie": "UMLS:C0160454", "names": ["Peritoneum injury with open wound into cavity", "Injury to peritoneum with open wound into cavity", "injury of peritoneum with open wound into cavity", "Injury to Peritoneum with Open Wound into Cavity", "Peritoneum injury with open wound into cavity (disorder)", "Injury of peritoneum with open wound into abdominal cavity", "injury of peritoneum with open wound into cavity (diagnosis)", "Injury to other intra-abdominal organs with open wound into cavity, peritoneum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peritoneum injury with open wound into cavity", "shortest_name_length": 45}
{"curie": "UMLS:C5421303", "names": ["Recurrent Primary Peritoneal Clear Cell Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Primary Peritoneal Clear Cell Adenocarcinoma", "shortest_name_length": 54}
{"curie": "UMLS:C0751501", "names": ["Intracranial Sinus Thrombophlebitis", "Sinus Thrombophlebitis, Intracranial", "Thrombophlebitis, Intracranial Sinus", "Intracranial Sinus Thrombophlebitides", "Sinus Thrombophlebitides, Intracranial", "Thrombophlebitides, Intracranial Sinus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intracranial Sinus Thrombophlebitis", "shortest_name_length": 35}
{"curie": "UMLS:C5206632", "names": ["Refractory Gastroesophageal Junction Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Gastroesophageal Junction Adenocarcinoma", "shortest_name_length": 51}
{"curie": "UMLS:C5420192", "names": ["Laryngeal Granular Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laryngeal Granular Cell Tumor", "shortest_name_length": 29}
{"curie": "MONDO:0100446", "names": ["ACHM3", "ACHM1", "RMCH1", "achromatopsia 3", "ACHM1, formerly", "RMCH1 (formerly)", "ACHM1 (formerly)", "CNGB3 retinopathy", "rod monochromacy 1", "CNGB3 achromatopsia", "rod monochromatism 1", "achromatopsia type 3", "CNGB3-related retinopathy", "achromatopsia with myopia", "rod monochromacy 1, formerly", "Rod monochromacy 1 (formerly)", "rod monochromatism 1, formerly", "Rod monochromatism 1 (formerly)", "total colorblindness with myopia", "achromatopsia caused by mutation in CNGB3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CNGB3-related retinopathy", "shortest_name_length": 5}
{"curie": "MONDO:0022820", "names": ["congenital articular rigidity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital articular rigidity", "shortest_name_length": 29}
{"curie": "UMLS:C1511261", "names": ["Borderline Ovarian Clear Cell Tumor", "Borderline Ovarian Clear Cell Neoplasm", "Clear cell cystic tumor of borderline malignancy", "ovarian clear cell tumor with proliferating activity", "clear cell tumor with proliferating activity, ovarian", "mesonephroid tumor with proliferating activity, ovarian"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Ovarian Clear Cell Tumor", "shortest_name_length": 35}
{"curie": "MONDO:0013742", "names": ["FEB11", "febrile seizures, familial, 11", "febrile seizures, familial, type 11", "familial mesial temporal lobe epilepsy with febrile seizures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial mesial temporal lobe epilepsy with febrile seizures", "shortest_name_length": 5}
{"curie": "UMLS:C4288890", "names": ["Infectious Hidradenitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infectious Hidradenitis", "shortest_name_length": 23}
{"curie": "UMLS:C0270807", "names": ["Congenital monoplegia", "congenital; monoplegia", "monoplegic cerebral palsy", "Monoplegic Cerebral Palsy", "Monoplegic cerebral palsy", "Cerebral Palsy, Monoplegic", "Monoplegic Cerebral Palsies", "Cerebral Palsies, Monoplegic", "paralysis; cerebral, monoplegic", "cerebral; paralysis, monoplegic", "Monoplegic cerebral palsy (disorder)", "monoplegic cerebral palsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Monoplegic Cerebral Palsy", "shortest_name_length": 21}
{"curie": "MONDO:0014780", "names": ["HPMRS4", "HPMRS6", "GPIBD40", "GPIBD12", "GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 12", "glycosylphosphatidylinositol biosynthesis defect 12", "glycosylphosphatidylinositol biosynthesis defect 40", "hyperphosphatasia with mental retardation syndrome 6", "hyperphosphatasia with mental retardation syndrome 4", "HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6", "PIGY hyperphosphatasia-intellectual disability syndrome", "hyperphosphatasia with intellectual disability syndrome 6", "hyperphosphatasia with mental retardation syndrome type 6", "hyperphosphatasia with intellectual disability syndrome type 6", "hyperphosphatasia with intellectual disability syndrome 6; HPMRS6", "hyperphosphatasia with impaired intellectual development syndrome 6", "HYPERPHOSPHATASIA WITH IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME 6", "hyperphosphatasia-intellectual disability syndrome caused by mutation in PIGY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperphosphatasia with intellectual disability syndrome 6", "shortest_name_length": 6}
{"curie": "MONDO:0020688", "names": ["Ischemic Myelopathy", "ischemic myelopathy", "Ischemic myelopathy", "Spinal Cord Ischemia", "myelopathy, ischemic", "Spinal cord ischemia", "Myelopathy, Ischemic", "spinal cord ischemia", "ischemia, spinal cord", "Ischemia, Spinal Cord", "Ischemic Myelopathies", "spinal cord; ischemic", "ischemia; spinal cord", "Spinal Cord Ischemias", "cord ischemia, spinal", "Spinal cord ischaemia", "ischemic myelopathies", "Cord Ischemia, Spinal", "spinal cord Ischemias", "cord Ischemias, spinal", "Ischemias, Spinal Cord", "Myelopathies, Ischemic", "Cord Ischemias, Spinal", "ischemias, spinal cord", "myelopathies, ischemic", "Ischemia of spinal cord", "Ischaemia of spinal cord", "Ischemic disorder of spinal cord", "experimental spinal cord ischemia", "Ischaemic disorder of spinal cord", "spinal cord ischemia, experimental", "Ischemic disorder of spinal cord (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal cord ischemia", "shortest_name_length": 19}
{"curie": "UMLS:C4727179", "names": ["CSPC", "mHSPC", "Hormone-Sensitive Prostate Carcinoma", "Castration-Sensitive Prostate Carcinoma", "Metastatic Hormone-Sensitive Prostate Cancer (mHSPC)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Castration-Sensitive Prostate Carcinoma", "shortest_name_length": 4}
{"curie": "UMLS:C0268948", "names": ["Scrotal ulcer", "SCROTUM ULCER", "scrotum; ulcer", "ulcer; scrotum", "Ulcer of scrotum", "SCROTAL ULCERATION", "Scrotum ulceration", "Ulcer of scrotum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ulcer of scrotum", "shortest_name_length": 13}
{"curie": "MONDO:0013253", "names": ["BROVCA3", "breast cancer, familial, susceptibility to, 3", "BREAST CANCER, FAMILIAL, SUSCEPTIBILITY TO, 3", "ovarian cancer, familial, susceptibility to, 3", "OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 3", "Rad51C hereditary breast ovarian cancer syndrome", "RAD51C hereditary breast ovarian cancer syndrome", "susceptibility to familial breast-ovarian cancer 3", "breast-ovarian cancer, familial, susceptibility to, 3", "BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 3", "breast-ovarian cancer, familial, susceptibility to, type 3", "hereditary breast ovarian cancer syndrome caused by mutation in Rad51C", "hereditary breast ovarian cancer syndrome caused by mutation in RAD51C"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast-ovarian cancer, familial, susceptibility to, 3", "shortest_name_length": 7}
{"curie": "MONDO:0017933", "names": ["hypertrophic cardiomyopathy and renal tubular disease due to mtDNA mutation", "hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation", "shortest_name_length": 75}
{"curie": "MONDO:0007802", "names": ["HYSP3", "hypospadias 3, autosomal", "HYPOSPADIAS 3, AUTOSOMAL", "Hypospadias 3, Autosomal", "hypospadias 3, autosomal, multifactorial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypospadias 3, autosomal", "shortest_name_length": 5}
{"curie": "UMLS:C3897521", "names": ["Stage IVA Oropharyngeal Lymphoepithelioma", "Stage IVA Oropharyngeal Lymphoepithelioma AJCC v7", "Stage IVA Oropharyngeal Undifferentiated Carcinoma", "Stage IVA Undifferentiated Oropharyngeal Throat Cancer", "Stage IVA Oropharyngeal Undifferentiated Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Oropharyngeal Undifferentiated Carcinoma AJCC v7", "shortest_name_length": 41}
{"curie": "MONDO:0019441", "names": ["ATTR cardiomyopathy", "ATTRV122I amyloidosis", "ATTRV122I-related amyloidosis", "TTR-related cardiac amyloidosis", "Transthyretin amyloid cardiopathy", "transthyretin amyloid cardiopathy", "TTR-related amyloid cardiomyopathy", "Transthyretin related familial amyloid cardiomyopathy", "transthyretin-related familial amyloid cardiomyopathy", "Transthyretin-related familial amyloid cardiomyopathy", "Transthyretin related familial amyloid cardiomyopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ATTRV122I amyloidosis", "shortest_name_length": 19}
{"curie": "MONDO:0004350", "names": ["extraocular retinoblastoma", "Extraocular Retinoblastoma", "retinoblastoma, extraocular", "childhood metastatic retinoblastoma", "Childhood Metastatic Retinoblastoma", "pediatric extraocular retinoblastoma", "Pediatric Extraocular Retinoblastoma", "Childhood Extraocular Retinoblastoma", "childhood extraocular retinoblastoma", "extraocular retinoblastoma of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pediatric extraocular retinoblastoma", "shortest_name_length": 26}
{"curie": "UMLS:C4553694", "names": ["IVA", "Stage IVA Cervical Cancer", "Stage IVA Cervical Cancer AJCC v8", "Stage IVA Cervical Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Cervical Cancer AJCC v8", "shortest_name_length": 3}
{"curie": "MONDO:0030930", "names": ["NEDEGE", "NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT EARLY-ONSET GENERALIZED EPILEPSY", "neurodevelopmental disorder with or without early-onset generalized epilepsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with or without early-onset generalized epilepsy", "shortest_name_length": 6}
{"curie": "UMLS:C1332889", "names": ["Central Nervous System Neuroepithelial Neoplasm of Uncertain Origin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Neuroepithelial Neoplasm of Uncertain Origin", "shortest_name_length": 67}
{"curie": "MONDO:0018421", "names": ["SPG69", "autosomal recessive spastic paraplegia type 69"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive spastic paraplegia type 69", "shortest_name_length": 5}
{"curie": "MONDO:0013885", "names": ["MALNS", "SOTOS2", "Malan syndrome", "MALAN SYNDROME", "Sotos syndrome 2", "SOTOS2, FORMERLY", "Sotos syndrome type 2", "MALAN OVERGROWTH SYNDROME", "Malan overgrowth syndrome", "SOTOS SYNDROME 2, FORMERLY", "Malan overgrowth syndrome (disorder)", "Malan overgrowth syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malan overgrowth syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0018778", "names": ["intermediate Charcot-Marie-Tooth disease", "Charcot-Marie-Tooth disease intermediate type", "Charcot-Marie-Tooth disease dominant intermediate", "Charcot-Marie-Tooth disease recessive intermediate", "Intermediate hereditary motor and sensory neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intermediate Charcot-Marie-Tooth disease", "shortest_name_length": 40}
{"curie": "MONDO:0033046", "names": ["MGORS8", "MEIER-GORLIN SYNDROME 8", "Meier-Gorlin syndrome 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meier-Gorlin syndrome 8", "shortest_name_length": 6}
{"curie": "MONDO:0013110", "names": ["NCFTD", "Cerebral folate deficiency", "Low CSF 5-methyltetrahydrofolate", "cerebral folate deficiency syndrome", "cerebral folate transport deficiency", "Cerebral folate transport deficiency", "cerebral folate receptor alpha deficiency", "Cerebral folate transport deficiency (disorder)", "Reduced CSF 5-methyltetrahydrofolate concentration", "Decreased CSF 5-methyltetrahydrofolate concentration", "NEURODEGENERATION DUE TO CEREBRAL FOLATE TRANSPORT DEFICIENCY", "Neurodegeneration Due To Cerebral Folate Transport Deficiency", "Neurodegeneration due to cerebral folate transport deficiency", "neurodegeneration due to cerebral folate TRANSPORT deficiency", "Neurodegenerative syndrome due to cerebral folate transport deficiency", "neurodegenerative syndrome due to cerebral folate transport deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodegenerative syndrome due to cerebral folate transport deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0007154", "names": ["Bavm", "BAVM", "cerebral AVM", "Cerebral AVM/H", "intracranial AVM", "A-V malformation", "BRAIN AV MALFORMATION", "Malformation;A-V;brain", "Cerebral AV malformation", "cerebral AV malformation", "arteriovenous brain malformation", "arteriovenous brain malformations", "Arteriovenous malformation of brain", "cerebral arteriovenous malformation", "Cerebral Arteriovenous Malformation", "Cerebral arteriovenous malformation", "Malformation, Cerebral Arteriovenous", "cerebral arteriovenous malformations", "Arteriovenous Malformation, Cerebral", "CEREBRAL ARTERIOVENOUS MALFORMATIONS", "Cerebral arteriovenous malformations", "Cerebral Arteriovenous Malformations", "Arteriovenous Malformations, Cerebral", "Malformations, Cerebral Arteriovenous", "Arteriovenous malformation of brain NOS", "intracranial arteriovenous malformation", "Intracranial arteriovenous malformation", "Intracranial Arteriovenous Malformation", "arteriovenous malformations of the brain", "Arteriovenous Malformation, Intracranial", "ARTERIOVENOUS MALFORMATIONS OF THE BRAIN", "intracranial arteriovenous malformations", "Malformation, Intracranial Arteriovenous", "Intracranial Arteriovenous Malformations", "Malformations, Intracranial Arteriovenous", "Arteriovenous Malformations, Intracranial", "AVM - Cerebral arteriovenous malformation", "Cerebrovascular arteriovenous malformation", "AVM (Arteriovenous Malformation) Intracranial", "Cerebral arteriovenous malformation (disorder)", "Arteriovenous malformation of cerebral vessels", "Congenital cerebral arteriovenous malformation", "Cerebral Arteriovenous Malformation/Hemangioma", "cerebral arteriovenous malformation (diagnosis)", "arteriovenous malformation of the brain, somatic", "Congenital Intracranial Arteriovenous Malformations", "Intracranial Arteriovenous Malformations, Congenital", "intracranial hemorrhage in brain arteriovenous malformations, susceptibility to", "INTRACRANIAL HEMORRHAGE IN BRAIN ARTERIOVENOUS MALFORMATIONS, SUSCEPTIBILITY TO", "intracranial hemorrhage in brain cerebrovascular malformations, susceptibility to, somatic mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arteriovenous malformations of the brain", "shortest_name_length": 4}
{"curie": "MONDO:0000239", "names": ["adiaspirosis", "Adiaspirosis", "haplomycosis", "adiaspiromycosis", "Adiaspiromycosis", "ADIASPIROMYCOSIS", "Haplosporangiosis", "haplosporangiosis", "pulmonary adiaspiromycosis", "Pulmonary adiaspiromycosis", "Emmonsia crescens infection", "Adiaspiromycosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adiaspiromycosis", "shortest_name_length": 12}
{"curie": "MONDO:0013470", "names": ["FEB3B", "GEFS+7", "GEFSP7", "GEFS+, TYPE 7", "Gefs+, type 7", "FEBRILE SEIZURES, FAMILIAL, 3B", "febrile seizures, familial, 3B", "generalized epilepsy with febrile seizures plus 7", "generalised epilepsy with febrile seizures plus 7", "Generalized Epilepsy With Febrile Seizures Plus, 7", "SCN9A generalized epilepsy with febrile seizures plus", "generalized epilepsy with febrile seizures plus type 7", "generalised epilepsy with febrile seizures plus type 7", "GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 7", "generalized epilepsy with febrile seizures plus, type 7", "Generalized Epilepsy With Febrile Seizures Plus, Type 7", "generalized epilepsy with febrile seizures plus caused by mutation in SCN9A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "generalized epilepsy with febrile seizures plus, type 7", "shortest_name_length": 5}
{"curie": "UMLS:C1333613", "names": ["Fibrosarcoma NCI Grade 2", "Fibrosarcoma NCI Grade II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fibrosarcoma NCI Grade 2", "shortest_name_length": 24}
{"curie": "UMLS:C4683600", "names": ["Lugano Classification Stage II Bulky Childhood Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage II Bulky Childhood Hodgkin Lymphoma AJCC v8", "shortest_name_length": 71}
{"curie": "UMLS:C0338396", "names": ["Proteus meningitis", "Proteus meningitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Proteus meningitis", "shortest_name_length": 18}
{"curie": "MONDO:0003666", "names": ["fallopian tube endometrioid cancer", "fallopian tube endometrioid neoplasm", "fallopian tube endometrioid carcinoma", "Fallopian Tube Endometrioid Carcinoma", "endometrioid carcinoma of fallopian tube", "Endometrioid Carcinoma of Fallopian Tube", "fallopian tube endometrioid adenocarcinoma", "Fallopian Tube Endometrioid Adenocarcinoma", "endometrioid carcinoma of the fallopian tube", "Endometrioid Carcinoma of the Fallopian Tube", "Endometrioid Adenocarcinoma of Fallopian Tube", "endometrioid adenocarcinoma of fallopian tube", "Endometrioid Adenocarcinoma of the Fallopian Tube", "endometrioid adenocarcinoma of the fallopian tube", "endometrioid adenocarcinoma of fallopian tube (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fallopian tube endometrioid adenocarcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0006402", "names": ["basal cell adenocarcinoma", "Basal cell adenocarcinoma", "Basal Cell Adenocarcinoma", "Salivary Gland Basal Cell Adenocarcinoma", "salivary gland basal cell adenocarcinoma", "Basal Cell Adenocarcinoma of Salivary Gland", "basal cell adenocarcinoma of salivary gland", "Basal cell adenocarcinoma of salivary gland", "basal cell adenocarcinoma of the salivary gland", "Basal Cell Adenocarcinoma of the Salivary Gland", "saliva-secreting gland skin basal cell carcinoma", "skin basal cell carcinoma of saliva-secreting gland", "basal cell adenocarcinoma of salivary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "salivary gland basal cell adenocarcinoma", "shortest_name_length": 25}
{"curie": "UMLS:C0278571", "names": ["Stage III Mycosis Fungoides", "Mycosis Fungoides Stage III", "Mycosis fungoides stage III", "Stage III Mycosis Fungoides AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mycosis fungoides stage III", "shortest_name_length": 27}
{"curie": "UMLS:C0856024", "names": ["Splenic marginal zone lymphoma stage I", "Stage I Splenic Marginal Zone Lymphoma", "Splenic Marginal Zone Lymphoma Stage I", "Stage I Splenic Marginal Zone B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Splenic marginal zone lymphoma stage I", "shortest_name_length": 38}
{"curie": "UMLS:C2747853", "names": ["Injury associated with device"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury associated with device", "shortest_name_length": 29}
{"curie": "UMLS:C5552785", "names": ["Chondrosarcoma, Grade 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chondrosarcoma, Grade 1", "shortest_name_length": 23}
{"curie": "UMLS:C0280183", "names": ["recurrent grade 2 follicular lymphoma", "Recurrent Grade 2 Follicular Lymphoma", "Relapsed Grade II Follicular Lymphoma", "Recurrent Grade II Follicular Lymphoma", "Relapsed Follicular Mixed Cell Lymphoma", "relapsed follicular mixed cell lymphoma", "Recurrent Follicular Mixed Cell Lymphoma", "follicular mixed cell lymphoma, relapsed", "follicular mixed cell lymphoma, recurrent", "Relapsed Grade II Follicular Mixed Cell Lymphoma", "Recurrent Grade II Follicular Mixed Cell Lymphoma", "recurrent grade II follicular mixed cell lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Grade 2 Follicular Lymphoma", "shortest_name_length": 37}
{"curie": "UMLS:C1517805", "names": ["Leukemia (Antiquated)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leukemia (Antiquated)", "shortest_name_length": 21}
{"curie": "MONDO:0032685", "names": ["CASGID", "infantile cataract, skin abnormalities, glutamate excess, and impaired intellectual development", "INFANTILE CATARACT, SKIN ABNORMALITIES, GLUTAMATE EXCESS, AND IMPAIRED INTELLECTUAL DEVELOPMENT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile cataract, skin abnormalities, glutamate excess, and impaired intellectual development", "shortest_name_length": 6}
{"curie": "MONDO:0017715", "names": ["HAD Deficiency", "HADH Deficiency", "HADH DEFICIENCY", "SCHAD Deficiency", "HADHSC Deficiency", "M-SCHAD Deficiency", "SCHAD DEFICIENCY, FORMERLY", "Deficiency of beta-keto-reductase", "3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY", "3-hydroxyacyl-CoA dehydrogenase deficiency", "3-Hydroxyacyl-CoA Dehydrogenase Deficiency", "3-@HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY", "Deficiency of beta-hydroxyacyl dehydrogenase", "Deficiency of 3-hydroxyacyl-CoA dehydrogenase", "3-Hydroxyacyl-Coenzyme A Dehydrogenase Deficiency", "3-Alpha-Hydroxyacyl-Coenzyme A Dehydrogenase Deficiency", "Deficiency of 3-hydroxyacyl-CoA dehydrogenase (disorder)", "Short-chain L-3-hydroxy acyl-CoA dehydrogenase deficiency", "L-3-Alpha-Hydroxyacyl-CoA Dehydrogenase, Short Chain, Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "3-hydroxyacyl-CoA dehydrogenase deficiency", "shortest_name_length": 14}
{"curie": "UMLS:C1511281", "names": ["breast adenocarcinoma with spindle cell metaplasia", "Breast Adenocarcinoma with Spindle Cell Metaplasia", "adenocarcinoma of breast with spindle cell metaplasia", "adenocarcinoma of breast with spindle cell metaplasia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenocarcinoma of breast with spindle cell metaplasia", "shortest_name_length": 50}
{"curie": "MONDO:0017681", "names": ["erythrokeratoderma variabilis progressiva"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythrokeratoderma variabilis progressiva", "shortest_name_length": 41}
{"curie": "MONDO:0010133", "names": ["TDH2A", "Deficiency of iodinase", "Iodide Peroxidase Deficiency", "Thyroid Dyshormonogenesis 2A", "iodide peroxidase deficiency", "THYROID DYSHORMONOGENESIS 2A", "IODIDE PEROXIDASE DEFICIENCY", "thyroid dyshormonogenesis 2A", "thyroid peroxidase deficiency", "THYROID PEROXIDASE DEFICIENCY", "Thyroid Peroxidase Deficiency", "Deficiency of iodide peroxidase", "thyroid dyshormonogenesis type 2A", "TPO familial thyroid dyshormonogenesis", "Deficiency of iodide peroxidase (disorder)", "genetic defect in thyroid hormonogenesis 2A", "Thyroid Hormonogenesis, Genetic Defect in, 2A", "THYROID HORMONOGENESIS, GENETIC DEFECT IN, 2A", "thyroid hormonogenesis, genetic defect in, 2A", "hypothyroidism, congenital, due to dyshormonogenesis, 2A", "Hypothyroidism, Congenital, due to Dyshormonogenesis, 2A", "HYPOTHYROIDISM, CONGENITAL, DUE TO DYSHORMONOGENESIS, 2A", "familial thyroid dyshormonogenesis caused by mutation in TPO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid dyshormonogenesis 2A", "shortest_name_length": 5}
{"curie": "UMLS:C0454576", "names": ["Mixed aphasia", "Mixed Aphasia", "Mixed Aphasias", "Aphasia, Mixed", "Mixed dysphasia", "Mixed dysphasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aphasia, Mixed", "shortest_name_length": 13}
{"curie": "MONDO:0014521", "names": ["meak", "MEAK", "EPM7", "PME type 7", "progressive myoclonus epilepsy 7", "epilepsy, progressive myoclonic 7", "Epilepsy, Progressive Myoclonic 7", "EPILEPSY, PROGRESSIVE MYOCLONIC 7", "KCNC1 progressive myoclonic epilepsy", "progressive myoclonus epilepsy type 7", "progressive myoclonic epilepsy type 7", "Progressive myoclonus epilepsy type 7", "Progressive myoclonic epilepsy type 7", "epilepsy, progressive myoclonic type 7", "EPM7 - epilepsy progressive myoclonic 7", "Progressive myoclonic epilepsy type 7 (disorder)", "Progressive myoclonic epilepsy due to KV3.1 deficiency", "progressive myoclonic epilepsy due to KV3.1 deficiency", "progressive myoclonic epilepsy caused by mutation in KCNC1", "myoclonus epilepsy and ataxia due to potassium channel mutation", "Myoclonus epilepsy and ataxia due to potassium channel mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive myoclonic epilepsy type 7", "shortest_name_length": 4}
{"curie": "MONDO:0010806", "names": ["RP13", "RP 13", "retinitis pigmentosa 13", "RETINITIS PIGMENTOSA 13", "Retinitis Pigmentosa 13", "PRPF8 retinitis pigmentosa", "retinitis pigmentosa type 13", "retinitis pigmentosa caused by mutation in PRPF8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 13", "shortest_name_length": 4}
{"curie": "UMLS:C5419585", "names": ["Refractory Grade 3b Follicular Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Grade 3b Follicular Lymphoma", "shortest_name_length": 39}
{"curie": "UMLS:C3838951", "names": ["Chondrosarcoma, Grade 2", "Chondrosarcoma, grade 2", "Grade II Chondrosarcoma", "Intermediate Grade Chondrosarcoma", "Intermediate-Grade Chondrosarcoma", "Chondrosarcoma, grade 2 (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chondrosarcoma, grade 2", "shortest_name_length": 23}
{"curie": "MONDO:0013695", "names": ["HNPCC6", "TGFBR2 hereditary nonpolyposis colon cancer", "COLON CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6", "Colon Cancer, Hereditary Nonpolyposis, Type 6", "colon cancer, hereditary nonpolyposis, type 6", "hereditary nonpolyposis colorectal cancer type 6", "colorectal cancer, hereditary nonpolyposis, type 6", "Colorectal Cancer, Hereditary Nonpolyposis, Type 6", "COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6", "hereditary nonpolyposis colon cancer caused by mutation in TGFBR2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorectal cancer, hereditary nonpolyposis, type 6", "shortest_name_length": 6}
{"curie": "MONDO:0032693", "names": ["GAMOS8", "GALLOWAY-MOWAT SYNDROME 8", "Galloway-Mowat syndrome 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Galloway-Mowat syndrome 8", "shortest_name_length": 6}
{"curie": "MONDO:0011296", "names": ["MKS2", "Meckel syndrome 2", "Meckel syndrome type 2", "TMEM216 Meckel syndrome", "Meckel Syndrome, Type 2", "MECKEL SYNDROME, TYPE 2", "Meckel syndrome, type 2", "Meckel-Gruber Syndrome, Type 2", "MECKEL-GRUBER SYNDROME, TYPE 2", "Meckel-Gruber syndrome, type 2", "Meckel syndrome type 2 (diagnosis)", "Meckel syndrome caused by mutation in TMEM216"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meckel syndrome, type 2", "shortest_name_length": 4}
{"curie": "MONDO:0005820", "names": ["LF", "LASSA FEVER", "fever lassa", "Lassa Fever", "Lassa fever", "lassa fever", "Lassa Fevers", "Fever, Lassa", "fever; Lassa", "Lassa; fever", "Lassa Virus Infection", "Infection, Lassa Virus", "Lassa fever (disorder)", "Virus Infection, Lassa", "Lassa Virus Infections", "Lassa hemorrhagic fever", "Lassa fever (diagnosis)", "Lassa haemorrhagic fever"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lassa fever", "shortest_name_length": 2}
{"curie": "UMLS:C5206654", "names": ["Localized Lung Carcinoma", "Non-Metastatic Lung Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized Lung Carcinoma", "shortest_name_length": 24}
{"curie": "MONDO:0010218", "names": ["SRXX2", "46XX sex reversal 2", "46,XX SEX REVERSAL 2", "46,XX SEX reversal 2", "46,XX sex reversal 2", "46,XX Sex reversal type 2", "chromosome 17q24 dupication syndrome", "CHROMOSOME 17q24 DUPLICATION SYNDROME", "chromosome 17Q24 Duplication syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XX sex reversal 2", "shortest_name_length": 5}
{"curie": "MONDO:0005692", "names": ["CSD", "debre's syndrome", "Debre's Syndrome", "scratch cat fever", "Cat-Scratch Fever", "cat-scratch fever", "Cat Scratch Fever", "Cat scratch fever", "cat scratch fever", "CAT-SCRATCH FEVER", "Cat-scratch fever", "cat fever scratch", "CAT SCRATCH FEVER", "Fever, Cat Scratch", "Catscratch Disease", "FEVER, CAT-SCRATCH", "catscratch disease", "Cat Scratch Fevers", "Scratch Fever, Cat", "Cat-Scratch Disease", "CAT SCRATCH DISEASE", "Cat scratch disease", "CAT-SCRATCH DISEASE", "cat disease scratch", "Cat-scratch disease", "Catscratch Diseases", "cat scratch disease", "cat-scratch disease", "Cat Scratch Disease", "Cat-Scratch Diseases", "cat-scratch; disease", "Cat Scratch Diseases", "Scratch Disease, Cat", "Scratch Diseases, Cat", "debre-Mollaret syndrome", "Debre-Mollaret Syndrome", "benign lymphoreticulosis", "Benign lymphoreticulosis", "lymphoreticulosis; benign", "CSD - Cat scratch disease", "catscratch disease or fever", "Bartonella henselae Infection", "Inoculative Lymphoreticuloses", "Inoculative Lymphoreticulosis", "Inoculation Lymphoreticuloses", "Inoculation Lymphoreticulosis", "Bartonella henselae Infections", "Lymphoreticulosis, Inoculative", "Lymphoreticuloses, Inoculative", "Lymphoreticuloses, Inoculation", "Lymphoreticulosis, Inoculation", "Cat scratch disease (disorder)", "Infection, Bartonella henselae", "Infections, Bartonella henselae", "cat scratch disease (diagnosis)", "Foshay-Mollaret Cat Scratch Fever", "Foshay-Mollaret Cat scratch fever", "disease (or disorder); cat-scratch", "Benign inoculation lymphoreticulosis", "Benign lymphoreticulosis, inoculation", "LYMPHORETICULOSIS, INOCULATION, BENIGN", "bartonellosis due to Bartonella henselae infection", "Bartonellosis due to Bartonella henselae infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cat-scratch disease", "shortest_name_length": 3}
{"curie": "MONDO:0016684", "names": ["Grade 3 Astrocytoma", "Grade III Astrocytoma", "astrocytoma grade iii", "Astrocytoma malignant", "malignant astrocytoma", "Malignant Astrocytoma", "Malignant astrocytoma", "grade III astrocytoma", "anaplastic astrocytoma", "Anaplastic astrocytoma", "Grade III Astrocytomas", "Anaplastic Astrocytoma", "High Grade Astrocytoma", "Astrocytoma, Grade III", "High-grade astrocytoma", "High-Grade Astrocytoma", "Astrocytoma, anaplastic", "anaplastic astrocytomas", "Astrocytomas, Grade III", "Anaplastic Astrocytomas", "Astrocytoma, Anaplastic", "Grade 3 Astrocytic Tumor", "Astrocytoma malignant NOS", "grade III Astrocytic tumor", "Grade III Astrocytic Tumor", "grade III astrocytic tumor", "Anaplastic Astrocytoma, NOS", "Grade 3 Astrocytic Neoplasm", "High-grade astrocytoma, NOS", "Astrocytoma, anaplastic type", "Grade III Astrocytic Neoplasm", "grade III astrocytic neoplasm", "astrocytoma, anaplastic, malignant", "Anaplastic Astrocytoma, Not Otherwise Specified", "Astrocytoma, anaplastic (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anaplastic astrocytoma", "shortest_name_length": 19}
{"curie": "MONDO:0006601", "names": ["Gibert", "PITYRIASIS ROSEA", "Pityriasis Rosea", "pityriasis rosea", "Pityriasis rosea", "rosea pityriasis", "pityriasis roseas", "pityriasis; rosea", "rosea; pityriasis", "Pityriasis circinata", "PR - Pityriasis rosea", "circinata; pityriasis", "pityriasis; circinata", "Pityriasis rosea (disorder)", "pityriasis rosea (diagnosis)", "Pityriasis circinata et maculata"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pityriasis rosea", "shortest_name_length": 6}
{"curie": "UMLS:C1511266", "names": ["Borderline Ovarian Serous Adenofibroma", "Serous adenofibroma of borderline malignancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Ovarian Serous Adenofibroma", "shortest_name_length": 38}
{"curie": "MONDO:0011699", "names": ["IBD8", "Inflammatory Bowel Disease 8", "INFLAMMATORY BOWEL DISEASE 8", "inflammatory bowel disease 8", "inflammatory bowel disease type 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory bowel disease 8", "shortest_name_length": 4}
{"curie": "MONDO:0700034", "names": ["mosaic trisomy 13", "trisomy 13 mosaicism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mosaic trisomy 13", "shortest_name_length": 17}
{"curie": "MONDO:0003211", "names": ["Nasal adenocarcinoma", "nasal cavity adenocarcinoma", "Nasal Cavity Adenocarcinoma", "Adenocarcinoma of Nasal Cavity", "adenocarcinoma of nasal cavity", "Adenocarcinoma of nasal cavity", "Adenocarcinoma of the Nasal Cavity", "Adenocarcinoma of the nasal cavity", "adenocarcinoma of the nasal cavity", "Adenocarcinoma of nasal cavity (disorder)", "adenocarcinoma of nasal cavity (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasal cavity adenocarcinoma", "shortest_name_length": 20}
{"curie": "UMLS:C0813148", "names": ["Endometrial carcinoma stage IV", "stage IV endometrial carcinoma", "endometrial carcinoma, stage IV", "Endometrial carcinoma metastatic", "Carcinoma endometrial metastatic", "Metastatic Endometrial Carcinoma", "endometrial carcinoma, metastatic", "stage IV carcinoma of the endometrium", "carcinoma of the endometrium, stage IV", "metastatic carcinoma of the endometrium", "carcinoma of the endometrium, metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Endometrial Carcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0013680", "names": ["CIAT", "COGNITIVE IMPAIRMENT WITH OR WITHOUT CEREBELLAR ATAXIA", "cognitive impairment with or without cerebellar ataxia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cognitive impairment with or without cerebellar ataxia", "shortest_name_length": 4}
{"curie": "MONDO:0010018", "names": ["SECOND METATARSAL-METACARPAL SYNDROME", "Second Metatarsal-Metacarpal Syndrome", "second metatarsal-metacarpal syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "second metatarsal-metacarpal syndrome", "shortest_name_length": 37}
{"curie": "MONDO:0008334", "names": ["PSORS1", "psoriasis 1", "HLA-C psoriasis", "PSORIASIS SUSCEPTIBILITY 1", "psoriasis susceptibility 1", "susceptibility to psoriasis 1", "psoriasis 1, susceptibility to", "PSORIASIS 1, SUSCEPTIBILITY TO", "psoriasis caused by mutation in HLA-C"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "psoriasis 1, susceptibility to", "shortest_name_length": 6}
{"curie": "MONDO:0700060", "names": ["leukemia, acute, X-linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukemia, acute, X-linked", "shortest_name_length": 25}
{"curie": "UMLS:C0521819", "names": ["Vaccination failure", "Inoculation failure", "Vaccination failure (finding)", "Suspected clinical vaccine failure", "Confirmed clinical vaccine failure", "Confirmed immunological vaccine failure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaccination failure", "shortest_name_length": 19}
{"curie": "MONDO:0020980", "names": ["Hair nevus", "Hair Nevus", "hair nevus", "hairy nevus", "Hair naevus", "Hairy nevus", "Hairy Nevus", "NEVUS HAIRY", "Hairy naevus", "hairy naevus", "Nevoid hypertrichosis", "Nevoid Hypertrichosis", "Hair nevus (disorder)", "nevoid hypertrichosis", "Naevoid hypertrichosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hair nevus", "shortest_name_length": 10}
{"curie": "UMLS:C2217037", "names": ["Stage IIIA Colon Cancer", "Stage IIIA Colon Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Colon Cancer AJCC v7", "shortest_name_length": 23}
{"curie": "UMLS:C0153329", "names": ["Tuberculosis Sequela", "TB - late effects of", "tuberculosis sequelae", "Tuberculosis Sequelae", "Sequela of Tuberculosis", "Sequelae of Tuberculosis", "Sequelae of tuberculosis", "sequelae of tuberculosis", "sequelae of; tuberculosis", "Tuberculosis late effects", "Tuberculosis late effects of", "late effects of tuberculosis", "Late effects of tuberculosis", "Sequelae of tuberculosis NOS", "Tuberculosis;late effects (of)", "Sequelae of tuberculosis (disorder)", "sequelae of tuberculosis (diagnosis)", "late effects of tuberculosis (diagnosis)", "tuberculosis; late effect of tuberculosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Late effects of tuberculosis", "shortest_name_length": 20}
{"curie": "MONDO:0011866", "names": ["Pch1", "PCH1A", "pontocerebellar hypoplasia type 1A", "pontocerebellar hypoplasia, type 1A", "VRK1 non-syndromic pontocerebellar hypoplasia", "pontocerebellar hypoplasia with anterior horn cell disease", "pontocerebellar hypoplasia with infantile spinal muscular atrophy", "non-syndromic pontocerebellar hypoplasia caused by mutation in VRK1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pontocerebellar hypoplasia type 1A", "shortest_name_length": 4}
{"curie": "MONDO:0022989", "names": ["diomedi bernardi placidi syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diomedi bernardi placidi syndrome", "shortest_name_length": 33}
{"curie": "MONDO:0019263", "names": ["EPP", "autosomal erythropoietic protoporphyria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal erythropoietic protoporphyria", "shortest_name_length": 3}
{"curie": "MONDO:0012479", "names": ["DIAR4", "ENTERIC ANENDOCRINOSIS", "enteric anendocrinosis", "Enteric Anendocrinosis", "Enteric anendocrinosis", "NEUROG3 congenital diarrhea", "congenital malabsorptive diarrhea 4", "congenital malabsorptive diarrhoea 4", "DIARRHEA 4, MALABSORPTIVE, CONGENITAL", "Diarrhea 4, Malabsorptive, Congenital", "diarrhea 4, malabsorptive, congenital", "congenital malabsorptive diarrhea type 4", "congenital diarrhea caused by mutation in NEUROG3", "congenital malabsorptive diarrhea due to paucity of enteroendocrine cells", "Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells", "congenital malabsorptive diarrhoea due to paucity of enteroendocrine cells", "Congenital malabsorptive diarrhoea due to paucity of enteroendocrine cells", "Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital malabsorptive diarrhea 4", "shortest_name_length": 5}
{"curie": "MONDO:0030925", "names": ["OOMD10", "OOCYTE MATURATION DEFECT 10", "oocyte maturation defect 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oocyte maturation defect 10", "shortest_name_length": 6}
{"curie": "UMLS:C4520918", "names": ["Stage IIB Soft Tissue Sarcoma", "Stage IIB Adult Sarcoma of Soft Tissue", "Stage IIB Adult Sarcoma of the Soft Tissue", "Stage IIB Adult Soft Tissue Sarcoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Adult Soft Tissue Sarcoma AJCC v7", "shortest_name_length": 29}
{"curie": "UMLS:C0853869", "names": ["Stage II Testicular Choriocarcinoma", "Testicular Choriocarcinoma Stage II", "Testicular choriocarcinoma stage II", "Stage II Testicular Choriocarcinoma AJCC v7", "Stage II Testicular Choriocarcinoma AJCC v6", "Stage II Testicular Choriocarcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular choriocarcinoma stage II", "shortest_name_length": 35}
{"curie": "MONDO:0006759", "names": ["Femoral neuropathy", "Femoral Neuropathy", "femoral neuropathy", "femoral nerve palsy", "Femoral nerve palsy", "nerve palsy femoral", "Neuropathy, Femoral", "femoral lesion nerve", "Femoral Neuropathies", "Femoral nerve lesion", "Femoral Nerve Disease", "femoral nerve lesions", "Femoral nerve lesions", "Femoral Nerve Diseases", "Femoral Mononeuropathy", "Nerve Disease, Femoral", "femoral nerve disorder", "femoral mononeuropathy", "Femoral nerve disorder", "Mononeuropathy, Femoral", "Nerve Diseases, Femoral", "Lesion of femoral nerve", "Femoral Mononeuropathies", "Femoral nerve lesion NOS", "femoral nerve dysfunction", "Lesion of femoral nerve, NOS", "Femoral neuropathy (disorder)", "femoral nerve palsy (diagnosis)", "disease (or disorder); femoral nerve", "femoral nerve peripheral nerve lesion", "peripheral nerve lesion of femoral nerve", "Lesion of femoral nerve, unspecified lower limb"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "femoral neuropathy", "shortest_name_length": 18}
{"curie": "MONDO:0013093", "names": ["GLM3", "glioblastoma 3", "BRCA2 malignant glioma", "GLIOMA SUSCEPTIBILITY 3", "glioma susceptibility 3", "glioma susceptibility type 3", "malignant glioma caused by mutation in BRCA2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glioma susceptibility 3", "shortest_name_length": 4}
{"curie": "MONDO:0017583", "names": ["mirror polydactyly-vertebral segmentation-limbs defects syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mirror polydactyly-vertebral segmentation-limbs defects syndrome", "shortest_name_length": 64}
{"curie": "MONDO:0012288", "names": ["IRIDOGONIODYSGENESIS AND SKELETAL ANOMALIES", "iridogoniodysgenesis and skeletal anomalies", "Iridogoniodysgenesis and skeletal anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "iridogoniodysgenesis and skeletal anomalies", "shortest_name_length": 43}
{"curie": "MONDO:0001209", "names": ["WART", "wart", "Wart", "Warts", "warts", "Wart(s)", "Verruca", "VERRUCA", "verruca", "VERRUCAE", "Verrucas", "Verrucae", "verrucas", "verrucae", "Wart, NOS", "Warts, NOS", "VERRUCA(E)", "wart viral", "viral wart", "Viral wart", "Mosaic wart", "warts viral", "COMMON WART", "viral Warts", "Common wart", "Common Wart", "common wart", "viral warts", "Viral warts", "Common warts", "Wart (viral)", "common warts", "Verruca, NOS", "mosaic warts", "verruca warts", "Warts (viral)", "Infectious wart", "Verruca simplex", "verruca simplex", "verruca vulgaris", "VERRUCA VULGARIS", "Viral warts, NOS", "Verruca vulgaris", "Infectious warts", "Verrucous Lesion", "Verruca Vulgaris", "verrucae vulgaris", "warts (diagnosis)", "Verrucous lesions", "VERRUCAE VULGARIS", "wartlike skin lesion", "Verrucous skin lesion", "SKIN LESION, WARTLIKE", "SKIN LESION, VERRUCOUS", "Viral warts (diagnosis)", "common warts (diagnosis)", "mosaic warts (diagnosis)", "verruca warts (diagnosis)", "Verrucous skin lesion, NOS", "Verruca vulgaris (disorder)", "clinical impressions wartlike", "Verruca (morphologic abnormality)", "viral Warts due to papilloma virus", "Viral warts due to papilloma virus", "wartlike skin lesion (physical finding)", "Viral warts due to human papillomavirus", "viral warts due to human papillomavirus", "Human papilloma virus infection of skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "common wart", "shortest_name_length": 4}
{"curie": "UMLS:C3890422", "names": ["PTLDS", "Chronic Lyme Disease", "Post-Treatment Lyme Disease", "Post Treatment Lyme Disease", "Lyme Disease, Post-Treatment", "Post Treatment Lyme Disease Syndrome", "Post-Treatment Lyme Disease Syndrome", "Post treatment Lyme disease syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post-Treatment Lyme Disease Syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0206172", "names": ["diabetic foot", "Diabetic Feet", "Diabetic Foot", "diabetic feet", "Diabetic foot", "DIABETIC FOOT", "diabetics feet", "Feet, Diabetic", "Foot, Diabetic", "Diabetic foot (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diabetic Foot", "shortest_name_length": 13}
{"curie": "MONDO:0022760", "names": ["22q monosomy", "monosomy 22q", "deletion 22q", "22q deletion", "partial monosomy 22q", "chromosome 22q deletion", "partial monosomy of chromosome 22q", "partial deletion of chromosome 22q", "partial monosomy of the long arm of chromosome 22", "partial deletion of the long arm of chromosome 22", "partial deletion of the long arm of chromosome type 22"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 22q deletion", "shortest_name_length": 12}
{"curie": "MONDO:0014971", "names": ["AI2A6", "amelogenesis imperfecta type 2A6", "Amelogenesis imperfecta, hypomaturation type, IIA6", "AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA6", "amelogenesis imperfecta, hypomaturation type, IIa6", "amelogenesis imperfecta, hypomaturation type, IIa6; AI2A6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amelogenesis imperfecta, hypomaturation type, IIa6", "shortest_name_length": 5}
{"curie": "MONDO:0015464", "names": ["Webster-Deming syndrome", "Webster Deming syndrome", "craniofrontonasal dysplasia-Poland anomaly syndrome", "Craniofrontonasal dysplasia-Poland anomaly syndrome", "Craniofrontonasal dysplasia with Poland anomaly syndrome", "Craniofrontonasal dysplasia with Poland anomaly syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniofrontonasal dysplasia-Poland anomaly syndrome", "shortest_name_length": 23}
{"curie": "OMIM:602025", "names": ["BMIQ9", "OBESITY, SUSCEPTIBILITY TO", "BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 5}
{"curie": "MONDO:0014927", "names": ["JBTS27", "Joubert syndrome 27", "JOUBERT SYNDROME 27", "B9D1 Joubert syndrome", "Joubert syndrome type 27", "Joubert syndrome caused by mutation in B9D1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome 27", "shortest_name_length": 6}
{"curie": "MONDO:0022752", "names": ["RSTS, Severe", "Rubinstein-Taybi syndrome, Severe", "Rubinstein-Taybi Syndrome, Severe", "Chromosome 16p13.3 Deletion Syndrome", "chromosome 16p13.3 deletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 16p13.3 deletion syndrome", "shortest_name_length": 12}
{"curie": "UMLS:C0677706", "names": ["Stage II Aggressive Non-Hodgkin Lymphoma", "stage II non-contiguous aggressive adult non-Hodgkin lymphoma", "aggressive, noncontiguous stage II adult non-Hodgkin lymphoma", "Stage II Non-Contiguous Aggressive Adult Non-Hodgkin Lymphoma", "Aggressive NonContiguous Adult Non-Hodgkin's Lymphoma Stage II", "aggressive noncontiguous adult non-Hodgkin's lymphoma stage II", "Stage II Aggressive NonContiguous Adult Non-Hodgkin's Lymphoma", "stage II aggressive noncontiguous adult non-Hodgkin's lymphoma", "aggressive non-contiguous stage II adult non-Hodgkin's lymphoma", "Stage II Non-Contiguous Aggressive Adult Non-Hodgkin's Lymphoma", "Stage II Aggressive Non-Contiguous Adult Non-Hodgkin's Lymphoma", "Aggressive Non-Contiguous Stage II Adult Non-Hodgkin's Lymphoma", "aggressive non-contiguous adult non-Hodgkin's lymphoma stage II", "stage II non-contiguous aggressive adult non-Hodgkin's lymphoma", "Aggressive Non-Contiguous Adult Non-Hodgkin's Lymphoma Stage II", "stage II aggressive non-contiguous adult non-Hodgkin's lymphoma", "Ann Arbor Stage II Non-Contiguous Aggressive Adult Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage II Non-Contiguous Aggressive Adult Non-Hodgkin Lymphoma", "shortest_name_length": 40}
{"curie": "UMLS:C0280481", "names": ["poor prognosis metastatic GTT", "metastatic GTT, poor prognosis", "GTT, poor prognosis, metastatic", "GTT, metastatic, poor prognosis", "trophoblastic tumor, metastatic, poor prognosis", "high risk metastatic gestational trophoblastic tumor", "Poor Prognosis Metastatic Gestational Trophoblastic Tumor", "poor prognosis metastatic gestational trophoblastic tumor", "gestational trophoblastic tumor, metastatic, poor prognosis", "gestational trophoblastic tumor, poor prognosis, metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Poor Prognosis Metastatic Gestational Trophoblastic Tumor", "shortest_name_length": 29}
{"curie": "MONDO:0002565", "names": ["myelitis", "Myelitis", "MYELITIS", "Myelitides", "Myelitis NOS", "Myelitis, NOS", "Myelitis (disorder)", "myelitis (diagnosis)", "Inflammatory Myelopathy", "spinal cord inflammation", "Spinal Cord Inflammation", "Myelopathy, Inflammatory", "SPINAL CORD INFLAMMATION", "inflammation; spinal cord", "spinal cord; inflammation", "Spinal Cord Inflammations", "Inflammation, Spinal Cord", "Inflammatory Myelopathies", "Myelopathies, Inflammatory", "Inflammations, Spinal Cord", "inflammation of spinal cord", "Inflammation of spinal cord"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myelitis", "shortest_name_length": 8}
{"curie": "UMLS:C5239028", "names": ["Metastatic High Grade Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic High Grade Sarcoma", "shortest_name_length": 29}
{"curie": "UMLS:C4764206", "names": ["Refractory Endometrial Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Endometrial Serous Adenocarcinoma", "shortest_name_length": 44}
{"curie": "UMLS:C2350037", "names": ["Clinically Isolated CNS Demyelinating Syndrome", "Clinically Isolated Syndrome, CNS Demyelinating"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinically Isolated Syndrome, CNS Demyelinating", "shortest_name_length": 46}
{"curie": "UMLS:C4329212", "names": ["17-Alpha-Hydroxylase/17,20 Lyase Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "17-Alpha-Hydroxylase/17,20 Lyase Deficiency", "shortest_name_length": 43}
{"curie": "UMLS:C0279963", "names": ["Stage I Burkitt Lymphoma", "stage I adult Burkitt lymphoma", "Stage I Adult Burkitt Lymphoma", "Stage I Adult Burkitt's Lymphoma", "Ann Arbor Stage I Adult Burkitt Lymphoma", "adult small noncleaved cell lymphoma, stage I", "Stage I Adult Diffuse Small Non-Cleaved Cell Lymphoma", "Adult Diffuse Small Non-Cleaved Cell Lymphoma Stage I", "stage I adult diffuse small noncleaved cell/Burkitt's lymphoma", "Adult Diffuse Small Non-Cleaved Cell/Burkitt's Lymphoma Stage I", "Stage I Adult Diffuse Small Non-Cleaved Cell/Burkitt's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Adult Burkitt Lymphoma", "shortest_name_length": 24}
{"curie": "MONDO:0004213", "names": ["Vulvar Non-Keratinizing Squamous Cell Carcinoma", "vulvar non-keratinizing squamous cell carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar non-keratinizing squamous cell carcinoma", "shortest_name_length": 47}
{"curie": "MONDO:0020537", "names": ["occupational allergic alveolitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "occupational allergic alveolitis", "shortest_name_length": 32}
{"curie": "MONDO:0008374", "names": ["RCD1", "retinal cone dystrophy 1", "Retinal Cone Dystrophy 1", "retinal cone dystrophy-1", "RETINAL CONE DYSTROPHY 1", "retinal cone Degeneration", "Retinal Cone Degeneration", "RETINAL CONE DEGENERATION", "retinal cone dystrophy type 1", "cone dystrophy autosomal dominant", "cone dystrophy, autosomal dominant", "Cone Dystrophy, Autosomal Dominant", "CONE DYSTROPHY, AUTOSOMAL DOMINANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal cone dystrophy type 1", "shortest_name_length": 4}
{"curie": "MONDO:0100270", "names": ["PEX19 related Zellweger spectrum disorder", "peroxisome biogenesis disorder due to PEX19 defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder due to PEX19 defect", "shortest_name_length": 41}
{"curie": "UMLS:C3494489", "names": ["Autoimmune polyendocrine syndrome, type 1", "Autoimmune polyendocrinopathy syndrome, type 1", "Hypoadrenocorticism with hypoparathyroidism and superficial moniliasis", "Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Autoimmune polyendocrinopathy syndrome, type 1", "shortest_name_length": 41}
{"curie": "UMLS:C0877094", "names": ["Application site bleeding", "Application site hemorrhage", "Application site haemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Application site hemorrhage", "shortest_name_length": 25}
{"curie": "UMLS:C5237255", "names": ["Patient-Specific Neoantigen-Positive Malignant Solid Tumor", "Patient-Specific Neoantigen-Positive Malignant Solid Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Patient-Specific Neoantigen-Positive Malignant Solid Neoplasm", "shortest_name_length": 58}
{"curie": "MONDO:0002366", "names": ["neoplasm of ANS", "autonomic nervous system tumor", "Autonomic Nervous System Tumor", "tumor of Autonomic nervous system", "Autonomic Nervous System Neoplasm", "tumor of autonomic nervous system", "Tumor of Autonomic Nervous System", "autonomic nervous system neoplasm", "Autonomic Nervous System Neoplasms", "autonomic nervous system neoplasms", "neoplasm of autonomic nervous system", "Neoplasm of Autonomic Nervous System", "tumor of the autonomic nervous system", "Tumor of the Autonomic Nervous System", "Neoplasm of the Autonomic Nervous System", "neoplasm of the autonomic nervous system", "Neoplasm of the autonomic nervous system", "autonomic nervous system neoplasm (disease)", "autonomic nervous system neoplasm (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autonomic nervous system neoplasm", "shortest_name_length": 15}
{"curie": "OMIM:112100", "names": [], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"]}
{"curie": "UMLS:C1142385", "names": ["functional ovarian cyst", "Functional Ovarian Cyst", "cyst functional ovarian", "Ovarian cyst functional", "Functional ovarian cyst", "ovarian cyst functional", "Functional Cyst of Ovary", "Functional cyst of ovary", "cysts functional ovarian", "Functional Cyst of the Ovary", "Functional cyst of ovary (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Functional cyst of ovary", "shortest_name_length": 23}
{"curie": "MONDO:0700186", "names": ["Feline Histiocytic Sarcoma", "feline histiocytic sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "feline histiocytic sarcoma", "shortest_name_length": 26}
{"curie": "MONDO:0017850", "names": ["siren", "Siren", "sympus", "Sympus", "sirens", "Symelia", "Symmelia", "Sympodia", "symmelia", "sympodia", "Symmelus", "sirenomelia", "Syrenomelus", "Sirenomelia", "SIRENOMELIA", "Sirenomelus", "Sympus apus", "sirenomelus", "Mermaid Syndrome", "mermaid syndrome", "Mermaid syndrome", "Syndrome, Mermaid", "Sirenoform monster", "Fused legs and feet", "Fused Legs and Feet", "Sirenomelia Sequence", "Mermaid Malformation", "Sirenomelia sequence", "mermaid malformation", "Sirenomelus sequence", "sirenomelia sequence", "Malformation, Mermaid", "Sequence, Sirenomelia", "Sirenomelia Sequences", "Sirenomelus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sirenomelia", "shortest_name_length": 5}
{"curie": "MONDO:0008760", "names": ["BKT", "T2 deficiency", "T2 Deficiency", "T2 DEFICIENCY", "MAT DEFICIENCY", "Mat deficiency", "3-Ktd deficiency", "3-KTD DEFICIENCY", "3-Alpha-Ktd Deficiency", "3-OXOTHIOLASE DEFICIENCY", "3-oxothiolase deficiency", "B-ketothiolase deficiency", "3-ketothiolase deficiency", "3-Ketothiolase deficiency", "3-KETOTHIOLASE DEFICIENCY", "3-Ketothiolase Deficiency", "B-Ketothiolase Deficiency", "3-@KETOTHIOLASE DEFICIENCY", "Beta-Ketothiolase Deficiency", "Beta ketothiolase deficiency", "BETA-KETOTHIOLASE DEFICIENCY", "Beta-ketothiolase deficiency", "beta-ketothiolase deficiency", "3-Alpha-Oxothiolase Deficiency", "peroxisomal thiolase deficiency", "Alpha-methylacetoaceticaciduria", "3-Alpha-Ketothiolase Deficiency", "3-Methylhydroxybutyric acidemia", "3-Methylhydroxybutyric Acidemia", "alpha-methylacetoaceticaciduria", "Alpha methylacetoacetic aciduria", "Alpha-Methylacetoacetic Aciduria", "3-Methylhydroxybutyric acidaemia", "ALPHA-METHYLACETOACETIC ACIDURIA", "ALPHA-methylacetoacetic aciduria", "alpha-Methylacetoacetic aciduria", "2-methyl-3-hydroxybutyricacidemia", "2-Methyl-3-hydroxybutyric acidemia", "2-Methyl-3-Hydroxybutyric Acidemia", "2-methyl-3-hydroxybutyric acidemia", "2-METHYL-3-HYDROXYBUTYRIC ACIDEMIA", "Acetoacetyl-CoA thiolase deficiency", "B-ketothiolase deficiency (diagnosis)", "Deficiency of acetoacetyl-CoA thiolase", "2-Alpha-Methyl-3-Hydroxybutyricacidemia", "Deficiency of acetyl-CoA acetyltransferase", "2-methyl-3-hydroxybutyric acidemia (diagnosis)", "Alpha-methyl-acetoacetyl-CoA thiolase deficiency", "Mitochondrial acetoacetyl-CoA Thiolase deficiency", "mitochondrial acetoacetyl-CoA thiolase deficiency", "mitochondrial acetoacetyl-Coa thiolase deficiency", "MITOCHONDRIAL ACETOACETYL-CoA THIOLASE DEFICIENCY", "Deficiency of acetyl-coenzyme A acetyltransferase", "Mitochondrial Acetoacetyl-CoA Thiolase deficiency", "mitochondrial acetoacetyl-coenzyme A thiolase deficiency", "Mitochondrial acetoacetyl-coenzyme A thiolase deficiency", "Deficiency of acetyl-coenzyme A acetyltransferase (disorder)", "Mitochondrial 2-methylacetoacetyl-CoA thiolase deficiency - potassium stimulated", "Mitochondrial 2-Methylacetoacetyl-Coa Thiolase Deficiency - Potassium Stimulated", "Mitochondrial 2-methylacetoacetyl-CoA thiolase deficiency - potassium stimulated (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "beta-ketothiolase deficiency", "shortest_name_length": 3}
{"curie": "UMLS:C0079581", "names": ["hypochlorhydria", "Hypochlorhydria", "HYPOCHLORHYDRIA", "Gastric hypoacidity", "hypoacidity; gastric", "Hypoacidity, gastric", "GASTRIC ACID DECREASED", "Gastric acid decreased", "Hypochlorhydria, gastric", "Decreased gastric acidity", "Gastric acidity, decreased", "Hypochlorhydria (disorder)", "hypochlorhydria (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypochlorhydria", "shortest_name_length": 15}
{"curie": "UMLS:C4524458", "names": ["Mucosal Melanoma of the Head and Neck"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mucosal Melanoma of the Head and Neck", "shortest_name_length": 37}
{"curie": "MONDO:0012150", "names": ["ADHD2", "ATTENTION DEFICIT-HYPERACTIVITY DISORDER, SUSCEPTIBILITY TO, 2", "attention deficit-hyperactivity disorder, susceptibility to, 2", "attention Deficit-hyperactivity disorder, susceptibility to, type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "attention deficit-hyperactivity disorder, susceptibility to, 2", "shortest_name_length": 5}
{"curie": "MONDO:0010244", "names": ["CGF1", "social cognition", "COGNITIVE FUNCTION 1, SOCIAL", "cognitive function 1, social"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CGF1", "shortest_name_length": 4}
{"curie": "UMLS:C4053765", "names": ["Schistosomiasis Nephropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Schistosomiasis Nephropathy", "shortest_name_length": 27}
{"curie": "UMLS:C4521825", "names": ["0", "Stage 0 Distal Bile Duct Cancer AJCC v8", "Stage 0 Distal Bile Duct Carcinoma AJCC v8", "Stage 0 Extrahepatic (Distal) Bile Duct Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Distal Bile Duct Cancer AJCC v8", "shortest_name_length": 1}
{"curie": "UMLS:C1335040", "names": ["Non-Neoplastic Retroperitoneal Disease", "Non-Neoplastic Retroperitoneal Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Retroperitoneal Disorder", "shortest_name_length": 38}
{"curie": "UMLS:C4525663", "names": ["Stage III Ileal Neuroendocrine Tumor", "Stage III Ileal Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Ileal Neuroendocrine Tumor AJCC v8", "shortest_name_length": 36}
{"curie": "MONDO:0000284", "names": ["Epidemic nephropathy", "Nephropathia epidemica", "Nephropathia Epidemica", "nephropathis epidemica", "NEPHROPATHIA EPIDEMICA", "nephropathia epidemica", "nephropathia epidemica (etiology)", "nephropathia epidemica (manifestation)", "Hantavirus hemorrhagic fever with renal syndrome, Puumala virus type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hantavirus hemorrhagic fever with renal syndrome, Puumala virus type", "shortest_name_length": 20}
{"curie": "MONDO:0007653", "names": ["genochondromatosis", "GENOCHONDROMATOSIS", "Genochondromatosis", "Genochondromatosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genochondromatosis", "shortest_name_length": 18}
{"curie": "MONDO:0009788", "names": ["optic atrophy, hearing loss, and peripheral neuropathy, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "optic atrophy, hearing loss, and peripheral neuropathy, autosomal recessive", "shortest_name_length": 75}
{"curie": "MONDO:0016290", "names": ["Hernández Aguirre-Negrete syndrome", "Hernandez Aguirre-Negrete syndrome", "Hernández-Aguirre Negrete syndrome", "Hernandez Aguirre Negrete syndrome", "intellectual disability-epilepsy-bulbous nose syndrome", "Intellectual disability-epilepsy-bulbous nose syndrome", "Intellectual disability, epilepsy, bulbous nose syndrome", "intellectual disability, epilepsy, bulbous nose syndrome", "Intellectual disability, epilepsy, bulbous nose syndrome (disorder)", "intellectual disability, epilepsy, bulbous nose syndrome (diagnosis)", "Ehlers-Danlos syndrome with progeroid facies and mild mental retardation", "Ehlers-Danlos syndrome with progeroid facies and mild intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hernández-Aguirre Negrete syndrome", "shortest_name_length": 34}
{"curie": "MONDO:0016936", "names": ["partial trisomy/tetrasomy of chromosome 18", "partial trisomy/tetrasomy of chromosome type 18", "partial duplication/triplication of chromosome 18"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial trisomy/tetrasomy of chromosome 18", "shortest_name_length": 42}
{"curie": "UMLS:C4289025", "names": ["Somatotroph/Lactotroph Adenoma", "Somatotroph-Lactotroph PitNET/Adenoma", "Growth Hormone and Prolactin-Producing Adenoma", "Somatotroph-Lactotroph Pituitary Neuroendocrine Tumor", "Somatotroph-Lactotroph Pituitary Neuroendocrine Tumor/Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Somatotroph-Lactotroph Pituitary Neuroendocrine Tumor", "shortest_name_length": 30}
{"curie": "MONDO:0021249", "names": ["Lip tumor", "Lip Tumor", "lip tumor", "Lip tumour", "lip tumors", "lip neoplasm", "tumor of Lip", "tumor of lip", "Lip neoplasm", "Lips--Tumors", "Lip Neoplasm", "Tumor of Lip", "Tumor of lip", "Tumour of lip", "lip neoplasms", "lips neoplasm", "Neoplasm, Lip", "Lip Neoplasms", "Neoplasms, Lip", "neoplasm of Lip", "Neoplasm of Lip", "neoplasm of lip", "Neoplasm of lip", "Lip neoplasm NOS", "tumor of the Lip", "Tumor of the lip", "Tumor of the Lip", "Tumour of the lip", "neoplasm of the Lip", "Neoplasm of the lip", "Neoplasm of the Lip", "Neoplasia of the lip", "lip neoplasm (disease)", "Neoplasm of lip (disorder)", "neoplasm of lip (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lip neoplasm", "shortest_name_length": 9}
{"curie": "UMLS:C0857175", "names": ["Postinfarction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postinfarction", "shortest_name_length": 14}
{"curie": "UMLS:C4525584", "names": ["Gastric Neuroendocrine Tumor by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Neuroendocrine Tumor by AJCC v8 Stage", "shortest_name_length": 45}
{"curie": "UMLS:C0854970", "names": ["Recurrent Lung Adenosquamous Carcinoma", "Adenosquamous cell lung cancer recurrent", "Adenosquamous Cell Lung Carcinoma Recurrent", "Recurrent Adenosquamous Cell Lung Carcinoma", "Recurrent Adenosquamous Cell Carcinoma of Lung", "Recurrent Adenosquamous Cell Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenosquamous cell lung cancer recurrent", "shortest_name_length": 38}
{"curie": "UMLS:C0270716", "names": ["Acquired hydrocephalus", "Acquired Hydrocephalus", "acquired hydrocephalus", "Hydrocephalus acquired", "Acquired hydrocephalus NOS", "Acquired hydrocephalus, NOS", "Acquired hydrocephalus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired hydrocephalus", "shortest_name_length": 22}
{"curie": "UMLS:C0855045", "names": ["Recurrent Extraosseous Ewing Sarcoma", "Recurrent Extraskeletal Ewing Sarcoma", "Relapsed Extra-Osseous Ewing's Sarcoma", "Recurrent Extraosseous Ewing's Sarcoma", "Recurrent Extra-Osseous Ewing's Sarcoma", "Recurrent Extraskeletal Ewing's Sarcoma", "Extra-osseous Ewing's sarcoma recurrent", "Extra-Osseous Ewing's Sarcoma, Recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extra-osseous Ewing's sarcoma recurrent", "shortest_name_length": 36}
{"curie": "UMLS:C0261439", "names": ["Accidental poisoning by methanol", "accidental poisoning by wood alcohol", "Accidental poisoning by wood alcohol", "Accidental poisoning by methyl alcohol", "accidental poisoning by methyl alcohol", "Accidental poisoning caused by methanol", "Accidental poisoning caused by wood alcohol", "Accidental poisoning caused by methyl alcohol", "accidental poisoning by wood alcohol (diagnosis)", "accidental poisoning by methyl alcohol (diagnosis)", "Accidental poisoning caused by methyl alcohol (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Accidental poisoning by methyl alcohol", "shortest_name_length": 32}
{"curie": "MONDO:0011720", "names": ["SPGF3", "SLC26A8 azoospermia", "spermatogenic failure 3", "SPERMATOGENIC FAILURE 3", "Nonobstructive azoospermia", "Azoospermia, nonobstructive", "Azoospermia, Nonobstructive", "spermatogenic failure type 3", "azoospermia caused by mutation in SLC26A8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 3", "shortest_name_length": 5}
{"curie": "MONDO:0032905", "names": ["SPG81", "spastic paraplegia 81, autosomal recessive", "SPASTIC PARAPLEGIA 81, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic paraplegia 81, autosomal recessive", "shortest_name_length": 5}
{"curie": "UMLS:C5418827", "names": ["Recurrent Extracranial Malignant Solid Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Extracranial Malignant Solid Neoplasm", "shortest_name_length": 47}
{"curie": "UMLS:C0855075", "names": ["Hodgkin's disease lymphocyte predominance type refractory", "Refractory Hodgkin's Disease Lymphocyte Predominance Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's disease lymphocyte predominance type refractory", "shortest_name_length": 57}
{"curie": "MONDO:0006786", "names": ["chiari syndrome", "chiari syndromes", "chiari's syndrome", "Budd-Chiari syndrome", "budd chiari syndrome", "budd-chiari syndrome", "budd chiari's syndrome", "v.hepatica; thrombosis", "Hepatic Vein Thromboses", "hepatic vein thrombosis", "Hepatic Vein Thrombosis", "Hepatic vein thrombosis", "thrombosis; hepatic vein", "HEPATIC VEIN OBSTRUCTION", "hepatic vein obstruction", "Vein Thromboses, Hepatic", "Thromboses, Hepatic Vein", "Blood clot in liver vein", "Thrombosis, Hepatic Vein", "Vein Thrombosis, Hepatic", "Hepatic venous thrombosis", "Hepatic vein thrombosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatic vein thrombosis", "shortest_name_length": 15}
{"curie": "MONDO:0012283", "names": ["CLEFT PALATE, MIDFACIAL HYPOPLASIA, TRIANGULAR FACIES, AND SENSORINEURAL HEARING LOSS", "cleft palate, midfacial hypoplasia, triangular facies, and sensorineural hearing loss", "Cleft palate, midfacial hypoplasia, triangular facies, and sensorineural hearing loss", "Unusual triangular facies associated with cleft palate, malocclusion, midfacial hypoplasia and sensorineural hearing loss"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleft palate, midfacial hypoplasia, triangular facies, and sensorineural hearing loss", "shortest_name_length": 85}
{"curie": "UMLS:C0853011", "names": ["diabetic hyperglycemic coma", "Diabetic hyperglycemic coma", "diabetic hyperglycaemic coma", "Diabetic hyperglycaemic coma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diabetic hyperglycemic coma", "shortest_name_length": 27}
{"curie": "MONDO:0020382", "names": ["multifocal pattern dystrophy simulating Stargardt disease", "Multifocal pattern dystrophy simulating Stargardt disease", "Multifocal pattern dystrophy simulating fundus flavimaculatus", "multifocal pattern dystrophy simulating fundus flavimaculatus", "Multifocal pattern dystrophy of retinal pigment epithelium simulating fundus flavimaculatus", "Multifocal pattern dystrophy of retinal pigment epithelium simulating fundus flavimaculatus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multifocal pattern dystrophy simulating fundus flavimaculatus", "shortest_name_length": 57}
{"curie": "MONDO:0016559", "names": ["megalocornea-spherophakia-secondary glaucoma syndrome", "glaucoma secondary to spherophakia/ectopia lentis and megalocornea"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glaucoma secondary to spherophakia/ectopia lentis and megalocornea", "shortest_name_length": 53}
{"curie": "MONDO:0016938", "names": ["Duplication of chromosome 20", "Partial trisomy of chromosome 20", "partial trisomy of chromosome 20", "Partial duplication of chromosome 20", "partial duplication of chromosome 20", "partial trisomy of chromosome type 20", "Partial trisomy of chromosome 20 (disorder)", "partial trisomy of chromosome 20 (diagnosis)", "anomaly of chromosome pair 20 partial trisomy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial trisomy of chromosome 20", "shortest_name_length": 28}
{"curie": "UMLS:C4683014", "names": ["Stage II Eyelid Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Eyelid Carcinoma AJCC v8", "shortest_name_length": 33}
{"curie": "MONDO:0021636", "names": ["Astroglioma", "astrocytoma", "astroglioma", "Astrocytic tumor", "Astrocytic Tumor", "astrocytic tumor", "astrocytic neoplasm", "Astrocytic Neoplasm", "astrocytoma of brain", "cerebral astrocytoma", "malignant astrocytoma", "astrocytoma of Cerebrum", "astrocytoma of cerebrum", "astrocytoma, no ICD-O subtype", "Diffuse Astrocytoma, IDH-Mutant", "Diffuse astrocytoma, IDH-mutant", "Diffuse Astrocytoma, IDH Mutant", "Astrocytoma, IDH-Mutant, Grade 2", "astrocytoma, IDH-mutant, grade 2", "Astrocytoma, IDH-Mutant, Grade II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "astrocytic tumor", "shortest_name_length": 11}
{"curie": "MONDO:0020007", "names": ["absence of the pulmonary artery"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "absence of the pulmonary artery", "shortest_name_length": 31}
{"curie": "UMLS:C4761078", "names": ["Philadelphia positive chronic myeloid leukemia", "Philadelphia positive chronic myeloid leukaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Philadelphia positive chronic myeloid leukemia", "shortest_name_length": 46}
{"curie": "UMLS:C2733598", "names": ["Disorder of lumbar disc", "Disorder of lumbar disc (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disorder of lumbar disc", "shortest_name_length": 23}
{"curie": "UMLS:C1868754", "names": ["Procedural dizziness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Procedural dizziness", "shortest_name_length": 20}
{"curie": "UMLS:C1335000", "names": ["Non-Neoplastic Central Nervous System Disease", "Non-Neoplastic Central Nervous System Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Central Nervous System Disorder", "shortest_name_length": 45}
{"curie": "UMLS:C5554579", "names": ["Advanced Cervical Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Cervical Squamous Cell Carcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0024322", "names": ["glycosylation disease", "disorder of glycosylation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of glycosylation", "shortest_name_length": 21}
{"curie": "MONDO:0006659", "names": ["ARTERIOSCLEROSIS OBLITERANS", "Arteriosclerosis obliterans", "Arteriosclerosis Obliterans", "arteriosclerosis obliterans", "Obliterans, Arteriosclerosis", "Arteriosclerosis obliterans (disorder)", "arteriosclerosis obliterans (diagnosis)", "arteriosclerosis obliterans (disorder) [ambiguous]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arteriosclerosis obliterans", "shortest_name_length": 27}
{"curie": "MONDO:0030534", "names": ["HH26", "HYPOGONADOTROPIC HYPOGONADISM 26 WITH OR WITHOUT ANOSMIA", "hypogonadotropic hypogonadism 26 with or without anosmia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadotropic hypogonadism 26 with or without anosmia", "shortest_name_length": 4}
{"curie": "UMLS:C5418952", "names": ["Recurrent Triple-Negative Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Triple-Negative Breast Carcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0005120", "names": ["Drosophila C virus infection", "Drosophila C virus infectious disease", "Drosophila C virus disease or disorder", "Drosophila C virus caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drosophila C virus infection", "shortest_name_length": 28}
{"curie": "UMLS:C5239289", "names": ["Locally Advanced Pancreatic Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Pancreatic Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0008348", "names": ["Pulmonary pseudolymphoma", "pulmonary pseudolymphoma", "Nodular Lymphoid Hyperplasia of Lung", "Nodular lymphoid hyperplasia of lung", "Pulmonary nodular lymphoid hyperplasia", "pulmonary nodular lymphoid hyperplasia", "Nodular lymphoid hyperplasia of lung (disorder)", "pulmonary nodular lymphoid hyperplasia, familial", "PULMONARY NODULAR LYMPHOID HYPERPLASIA, FAMILIAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary nodular lymphoid hyperplasia", "shortest_name_length": 24}
{"curie": "UMLS:C0156228", "names": ["Nephrotic Syndrome with Lesion of Membranous Glomerulonephritis", "Nephrotic syndrome with lesion of membranous glomerulonephritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome with Lesion of Membranous Glomerulonephritis", "shortest_name_length": 63}
{"curie": "MONDO:0013707", "names": ["MRT24", "mental retardation, autosomal recessive 24", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 24", "intellectual disability, autosomal recessive 24", "autosomal recessive intellectual developmental disorder 24", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 24"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 24", "shortest_name_length": 5}
{"curie": "MONDO:0011682", "names": ["EA3", "Episodic ataxia type 3", "episodic ataxia type 3", "Episodic Ataxia, Type 3", "EPISODIC ATAXIA, TYPE 3", "episodic ataxia, type 3", "Episodic ataxia type 3 (disorder)", "Ataxia, Episodic, With Vertigo And Tinnitus", "ATAXIA, EPISODIC, WITH VERTIGO AND TINNITUS", "ataxia, episodic, with vertigo and tinnitus", "episodic ataxia-vertigo-tinnitus-myokymia syndrome", "Episodic ataxia-vertigo-tinnitus-myokymia syndrome", "Episodic ataxia and vertigo with tinnitus and myokymia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "episodic ataxia type 3", "shortest_name_length": 3}
{"curie": "MONDO:0010805", "names": ["Ectopia Vesicae", "Ectopia vesicae", "ectopia vesicae", "Bladder Extrophy", "bladder extrophy", "ectopia; bladder", "bladder eversion", "ectopia; vesicae", "extrophy bladder", "vesicae; ectopia", "bladder; ectopia", "Extrophy, Bladder", "BLADDER EXSTROPHY", "bladder exstrophy", "eversion; bladder", "Bladder exstrophy", "Bladder Exstrophy", "bladder; eversion", "bladder; exstrophy", "Exstrophy, Bladder", "exstrophy; bladder", "Bladder Extrophies", "Extrophies, Bladder", "Bladder Exstrophies", "Exstrophies, Bladder", "EXSTROPHY OF BLADDER", "Exstrophy of bladder", "Exstrophy Of Bladder", "exstrophy of bladder", "extroversion; bladder", "bladder; extroversion", "Extroversion of bladder", "exstrophy of the bladder", "Exstrophy of the Bladder", "Urinary Bladder Exstrophy", "urinary bladder exstrophy", "Ectopic bladder congenital", "Exstrophy, Urinary Bladder", "Congenital ectopic bladder", "Urinary Bladder Exstrophies", "bladder exstrophy (disease)", "Exstrophy of urinary bladder", "bladder eversion (diagnosis)", "exstrophy of urinary bladder", "Exstrophies, Urinary Bladder", "bladder exstrophy (diagnosis)", "Exstrophy of bladder sequence", "classic exstrophy of the bladder", "Classic exstrophy of the bladder", "bladder exstrophy (physical finding)", "bladder exstrophy and epispadias Complex", "Exstrophy of bladder sequence (disorder)", "Exstrophy of urinary bladder, unspecified", "exteriorized; bladder (mucosa), congenital", "Congenital extroversion of urinary bladder", "malposition; congenital, bladder, exteriorized or extroverted", "bladder; malposition, congenital (exteriorized or extroverted)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder exstrophy", "shortest_name_length": 15}
{"curie": "UMLS:C4521738", "names": ["0", "Stage 0 Esophageal Squamous Cell Cancer", "Pathologic Stage 0 Esophageal Squamous Cell Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage 0 Esophageal Squamous Cell Carcinoma AJCC v8", "shortest_name_length": 1}
{"curie": "UMLS:C4289044", "names": ["Gastroesophageal Junction Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastroesophageal Junction Neuroendocrine Carcinoma", "shortest_name_length": 50}
{"curie": "MONDO:0003574", "names": ["external ear cancer", "cancer of external ear", "Malignant External Ear Tumor", "malignant external Ear tumor", "Malignant External Ear Neoplasm", "malignant tumor of external Ear", "External ear neoplasm malignant", "malignant external ear neoplasm", "malignant external Ear neoplasm", "malignant tumor of external ear", "Malignant Tumor of External Ear", "Malignant tumor of external ear", "Malignant tumour of external ear", "malignant neoplasm of external Ear", "malignant neoplasm of external ear", "Malignant Neoplasm of External Ear", "neoplasm of ear malignant external", "malignant tumor of the external Ear", "Malignant Tumor of the External Ear", "malignant neoplasm of the external Ear", "Malignant Neoplasm of the External Ear", "malignant neoplasm of the External ear", "malignant neoplasm of the external ear", "Malignant External Auditory Canal Neoplasm", "Malignant tumor of external ear (disorder)", "malignant neoplasm of external ear (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "external ear cancer", "shortest_name_length": 19}
{"curie": "UMLS:C5446878", "names": ["Breast Florid Lobular Carcinoma In Situ"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Florid Lobular Carcinoma In Situ", "shortest_name_length": 39}
{"curie": "MONDO:0017864", "names": ["Pulmonary Vein Stenoses", "pulmonary vein stenosis", "Pulmonary vein stenosis", "Pulmonary Vein Stenosis", "pulmonary stenosis veins", "Stenosis, Pulmonary Vein", "Vein Stenosis, Pulmonary", "Vein Stenoses, Pulmonary", "pulmonary veins stenosis", "Stenoses, Pulmonary Vein", "stenosis of pulmonary vein", "Pulmonary vein stenosis (disorder)", "stenosis of pulmonary vein (diagnosis)", "congenital pulmonary veins atresia or stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital pulmonary veins atresia or stenosis", "shortest_name_length": 23}
{"curie": "MONDO:0034143", "names": ["early-onset calcifying leukoencephalopathy-skeletal dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early-onset calcifying leukoencephalopathy-skeletal dysplasia", "shortest_name_length": 61}
{"curie": "UMLS:C5419513", "names": ["Locally Advanced Papillary Renal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Papillary Renal Cell Carcinoma", "shortest_name_length": 47}
{"curie": "MONDO:0016486", "names": ["Cooley", "Cooley anemia", "cooley anemia", "Cooley Anemia", "COOLEY ANEMIA", "Anemia, Cooley", "Cooley; anemia", "anemia; Cooley", "cooleys anemia", "cooley's anemia", "Cooley's Anemia", "Anemia, Cooleys", "anemia cooley's", "Cooley's anemia", "cooley's anaemia", "Anemia, Cooley's", "Cooley's anaemia", "Thalassemia major", "major thalassemia", "Thalassemia Major", "THALASSEMIA MAJOR", "thalassemia major", "Thalassaemia major", "thalassemia; major", "thalassaemia major", "major; thalassemia", "Mediterranean anemia", "mediterranean anemia", "Mediterranean Anemia", "Anemia, Mediterranean", "anemia; Mediterranean", "Mediterranean anaemia", "Mediterranean; anemia", "Mediterranean Anemias", "Erythroblastic Anemia", "mediterranean anaemia", "ANEMIA, MEDITERRANEAN", "beta-thalassemia major", "Beta Thalassemia Major", "Anemia, Erythroblastic", "beta thalassemia major", "Beta thalassemia Major", "Beta-thalassemia major", "Thalassemia major, NOS", "Beta thalassemia major", "Anemias, Mediterranean", "BETA THALASSEMIA MAJOR", "Homozygous thalassemia", "beta thalassaemia major", "Homozygous thalassaemia", "Beta thalassaemia major", "Anemias, Erythroblastic", "homozygous beta thalassemia", "Homozygous beta thalassemia", "Homozygous thalassemia, NOS", "Thalassemia major (disorder)", "Homozygous beta thalassaemia", "beta Thalassemia, homozygous", "thalassemia major (diagnosis)", "homozygous beta-thalassemia major", "major homozygous beta-thalassemia", "ANEMIA, HEMOLYTIC, THALASSEMIA MAJOR", "Homozygous beta thalassemia (disorder)", "Thalassemia Major (beta Thalassemia Major)", "Thalassemia Major (beta-Thalassemia Major)", "Major, Thalassemia (beta-Thalassemia Major)", "Thalassemia Majors (beta-Thalassemia Major)", "Majors, Thalassemia (beta-Thalassemia Major)", "homozygous beta-thalassemia major (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "beta-thalassemia major", "shortest_name_length": 6}
{"curie": "UMLS:C0238371", "names": ["phrenic nerve palsy", "Phrenic Nerve Palsy", "nerve palsy phrenic", "Phrenic nerve palsy", "Phrenic nerve lesion", "n.phrenicus; paralysis", "phrenic nerve paralysis", "Phrenic nerve paralysis", "PHRENIC NERVE PARALYSIS", "paralysis; phrenic nerve", "Paralysis of phrenic nerve", "Phrenic nerve lesion (disorder)", "phrenic nerve palsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Phrenic nerve lesion", "shortest_name_length": 19}
{"curie": "UMLS:C4763388", "names": ["PVRL", "Primary Vitreoretinal Lymphoma", "Primary Vitreoretinal Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Vitreoretinal Non-Hodgkin Lymphoma", "shortest_name_length": 4}
{"curie": "UMLS:C5420282", "names": ["Head and Neck Merkel Cell Carcinoma", "Head and Neck Lymph Nodes Merkel Cell Carcinoma", "Head and Neck Merkel Cell Carcinoma of Unknown Primary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Head and Neck Merkel Cell Carcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C1519911", "names": ["Vaginal Adenoid Basal Cancer", "Vaginal Adenoid Basal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Adenoid Basal Carcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0019530", "names": ["Syndactyly", "syndactyly", "symphalangy", "symphalangism", "webbing of digits", "isolated syndactyly", "nonsyndromic syndactyly", "non-syndromic syndactyly", "chromosome 2q35 duplication syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-syndromic syndactyly", "shortest_name_length": 10}
{"curie": "UMLS:C2931852", "names": ["Clear-cell metastatic renal cell carcinoma", "Metastatic Clear Cell Renal Cell Carcinoma", "Metastatic clear cell renal cell carcinoma", "Clear cell renal cell carcinoma metastatic", "Metastatic clear cell renal cell carcinoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clear-cell metastatic renal cell carcinoma", "shortest_name_length": 42}
{"curie": "UMLS:C5557394", "names": ["Advanced Lung Adenosquamous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Lung Adenosquamous Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0010970", "names": ["CPCMR", "cleft palate, CARDIAC defects, and mental retardation", "CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION", "cleft palate, cardiac defects, and mental retardation", "cleft palate, Cardiac defects, and mental retardation", "cleft palate, CARDIAC defects, and intellectual disability", "cleft palate, Cardiac defects, and intellectual disability", "cleft palate, cardiac defects, and intellectual disabillity", "CLEFT PALATE, CARDIAC DEFECTS, AND IMPAIRED INTELLECTUAL DEVELOPMENT", "Cardiac Malformation, Cleft Lip-Palate, Microcephaly and Digital Anomalies", "cardiac malformation, cleft lip/palate, microcephaly, and digital anomalies", "CARDIAC MALFORMATION, CLEFT LIP/PALATE, MICROCEPHALY, AND DIGITAL ANOMALIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiac malformation, cleft lip/palate, microcephaly, and digital anomalies", "shortest_name_length": 5}
{"curie": "UMLS:C5419423", "names": ["Tactile Disorder", "Tactile Disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tactile Disorder", "shortest_name_length": 16}
{"curie": "MONDO:0032916", "names": ["IMMAS", "IMAGAWA-MATSUMOTO SYNDROME", "Imagawa-Matsumoto syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Imagawa-Matsumoto syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0003982", "names": ["cancer in both breasts", "Bilateral Breast Cancer", "bilateral breast cancer", "Bilateral breast carcinoma", "bilateral breast carcinoma", "Bilateral Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bilateral breast carcinoma", "shortest_name_length": 22}
{"curie": "UMLS:C0280164", "names": ["Stage III Immunoblastic Lymphoma", "Stage III Adult Immunoblastic Lymphoma", "Ann Arbor Stage III Adult Immunoblastic Lymphoma", "stage III adult immunoblastic large cell lymphoma", "Stage III Adult Immunoblastic Large Cell Lymphoma", "Adult Immunoblastic Large Cell Lymphoma Stage III", "adult immunoblastic large cell lymphoma, stage III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Adult Immunoblastic Lymphoma", "shortest_name_length": 32}
{"curie": "UMLS:C0334038", "names": ["Gastric Metaplasia", "Gastric metaplasia", "gastric metaplasia", "Metaplasia, gastric", "Gastric metaplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric metaplasia", "shortest_name_length": 18}
{"curie": "MONDO:0019192", "names": ["AKT2-related FPLD", "AKT2-related familial partial lipodystrophy", "familial partial lipodystrophy due to AKT2 mutations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AKT2-related familial partial lipodystrophy", "shortest_name_length": 17}
{"curie": "MONDO:0033204", "names": ["CILD37", "primary ciliary dyskinesia 37", "ciliary dyskinesia, primary, 37", "CILIARY DYSKINESIA, PRIMARY, 37", "CILIARY DYSKINESIA, PRIMARY, 37, WITH OR WITHOUT SITUS INVERSUS", "ciliary dyskinesia, primary, 37, with or without situs inversus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ciliary dyskinesia, primary, 37", "shortest_name_length": 6}
{"curie": "UMLS:C4528215", "names": ["LyP with Chromosome 6p25 Rearrangement", "LyP with DUSP22-IRF4 Gene Rearrangement", "LyP with Chromosome 6p25.3 Rearrangement", "Lymphomatoid Papulosis with DUSP22-IRF4 Gene Rearrangement", "Lymphomatoid Papulosis with Chromosome 6p25.3 Rearrangement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphomatoid Papulosis with DUSP22-IRF4 Gene Rearrangement", "shortest_name_length": 38}
{"curie": "MONDO:0012644", "names": ["ATD2", "SRTD2", "IFT80 Jeune syndrome", "ASPHYXIATING THORACIC DYSTROPHY 2", "Asphyxiating Thoracic Dystrophy 2", "asphyxiating thoracic dystrophy 2", "asphyxiating thoracic dystrophy type 2", "Jeune syndrome caused by mutation in IFT80", "short-rib thoracic dysplasia 2 with or without polydactyly", "SHORT-RIB THORACIC DYSPLASIA 2 WITH OR WITHOUT POLYDACTYLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "asphyxiating thoracic dystrophy 2", "shortest_name_length": 4}
{"curie": "MONDO:0001109", "names": ["Petrositis", "petrositis", "Petrositides", "Petrositis, NOS", "acute petrositis", "Acute petrositis", "chronic petrositis", "Chronic petrositis", "Petrositis syndrome", "Petrositis (disorder)", "petrositis (diagnosis)", "Unspecified petrositis", "Petrositis, unspecified", "inflammation; petrous bone", "petrous bone; inflammation", "Acute petrositis (disorder)", "acute petrositis (diagnosis)", "Inflammation of petrous bone", "inflammation of petrous bone", "Chronic petrositis (disorder)", "chronic petrositis (diagnosis)", "Acute petrositis, unspecified ear", "Inflammation of petrous bone, NOS", "Chronic petrositis, unspecified ear", "Unspecified petrositis, unspecified ear", "petrous part of temporal bone inflammation", "inflammation of petrous part of temporal bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "petrositis", "shortest_name_length": 10}
{"curie": "MONDO:0018666", "names": ["HBL", "hepatoblastoma", "HEPATOBLASTOMA", "Hepatoblastoma", "Hepatoblastomas", "Embryonal hepatoma", "Hepatoblastoma NOS", "embryonal; hepatoma", "hepatoma; embryonal", "HBL - Hepatoblastoma", "Hepatoblastoma of liver", "hepatoblastoma of liver", "childhood hepatoblastoma", "pediatric hepatoblastoma", "Pediatric Hepatoblastoma", "hepatoblastoma, childhood", "hepatoblastoma, malignant", "HEPATOBLASTOMA, MALIGNANT", "Hepatoblastoma (disorder)", "Pediatric Embryonal Hepatoma", "pediatric embryonal hepatoma", "hepatoblastoma of liver (diagnosis)", "Hepatoblastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatoblastoma", "shortest_name_length": 3}
{"curie": "MONDO:0001828", "names": ["acquired color blindness", "Color blindness acquired", "Acquired color blindness", "Acquired Color Blindness", "Color Blindness, Acquired", "Acquired colour blindness", "Colour blindness acquired", "acquired colour blindness", "acquired color vision disorder", "acquired color vision deficiency", "Acquired color vision deficiency", "acquired colour vision deficiency", "Acquired colour vision deficiency", "acquired color vision deficiencies", "Acquired color vision deficiencies", "acquired colour vision deficiencies", "acquired color blindness (diagnosis)", "Acquired color vision deficiency, NOS", "Acquired colour vision deficiency, NOS", "Acquired color vision deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired color blindness", "shortest_name_length": 24}
{"curie": "MONDO:0022694", "names": ["cerebral calcifications opalescent teeth phosphaturia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral calcifications opalescent teeth phosphaturia", "shortest_name_length": 53}
{"curie": "MONDO:0004474", "names": ["gallbladder lymphoma", "Gallbladder Lymphoma", "gall bladder lymphoma", "lymphoma of gallbladder", "Lymphoma of Gallbladder", "lymphoma of gall bladder", "Lymphoma of the Gallbladder", "Lymphoma of the gallbladder", "lymphoma of the gallbladder", "primary gallbladder lymphoma", "Primary Gallbladder Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gallbladder lymphoma", "shortest_name_length": 20}
{"curie": "UMLS:C0042484", "names": ["vein distended", "distended veins", "vein engorgement", "Venous Congestion", "Venous congestion", "venous congestion", "Passive hyperemia", "Passive Hyperemia", "passive congestion", "Passive hyperaemia", "venous engorgement", "Congestion, Venous", "Venous Engorgement", "congestion; venous", "Hyperemia, Passive", "Passive Congestion", "Passive congestion", "Congestion, passive", "Engorgement, Venous", "venous; engorgement", "Passive congestion (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Venous Engorgement", "shortest_name_length": 14}
{"curie": "MONDO:0005470", "names": ["postprandial hypotension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postprandial hypotension", "shortest_name_length": 24}
{"curie": "MONDO:0012217", "names": ["BRKS2", "Bruck syndrome 2", "BRUCK SYNDROME 2", "Bruck syndrome, 2", "PLOD2 Bruck syndrome", "Bruck syndrome type 2", "Bruck syndrome caused by mutation in PLOD2", "OSTEOGENESIS IMPERFECTA WITH CONGENITAL JOINT CONTRACTURES", "osteogenesis imperfecta with congenital Joint contractures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bruck syndrome 2", "shortest_name_length": 5}
{"curie": "MONDO:0012827", "names": ["IS5", "SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 5", "scoliosis, isolated, susceptibility to, 5", "scoliosis, idiopathic, susceptibility to, 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scoliosis, isolated, susceptibility to, 5", "shortest_name_length": 3}
{"curie": "UMLS:C4725814", "names": ["Recurrent Malignant Thyroid Gland Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Malignant Thyroid Gland Neoplasm", "shortest_name_length": 42}
{"curie": "UMLS:C0158090", "names": ["pathological dislocation", "Pathological dislocation", "Dislocation of joint, NOS", "pathological; dislocation", "dislocation; pathological", "Pathologic Joint Dislocation", "Joint dislocation pathological", "Spontaneous dislocation of joint", "Pathological dislocation of joint", "pathological dislocation of joint", "Spontaneous dislocation of joint, NOS", "Pathological dislocation of joint, NOS", "Pathological dislocation of joint (disorder)", "pathological dislocation of joint (diagnosis)", "Pathological dislocation of joint, site unspecified", "Dislocation AND/OR displacement of joint, not due to injury", "Dislocation or displacement of joint, not recurrent and not current", "Dislocation or displacement of joint, not recurrent or current injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathological dislocation of joint", "shortest_name_length": 24}
{"curie": "MONDO:0016444", "names": ["Milian", "anetoderma", "Anetoderma", "Anetodermas", "macular atrophy", "Macular atrophy", "macular; atrophy", "atrophy; macular", "Milian's erythema", "Primary anetoderma", "primary anetoderma", "Primary Anetoderma", "Primary Anetodermas", "Anetoderma, Primary", "Anetodermas, Primary", "Anetoderma (disorder)", "anetoderma (diagnosis)", "Atrophoderma maculatum", "atrophoderma; maculatum", "maculatum; atrophoderma", "Primary macular atrophy", "primary macular atrophy", "Atrophic macular change", "atrophic macular change", "Atrophy blanche of Milian", "Atrophie blanche of Milian", "Primary anetoderma (disorder)", "atrophic macular change (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary anetoderma", "shortest_name_length": 6}
{"curie": "MONDO:0005645", "names": ["Ancylostomosis", "ankylostomiasis", "ANCYLOSTOMIASIS", "Ancylostomiases", "Ankylostomiasis", "Ancylostomiasis", "ancylostomiasis", "hookworm infection", "Hookworm infection", "Ancylostoma; infestation", "infestation; Ancylostoma", "infection by Ancylostoma", "Ancylostomiasis (disorder)", "Infection due to Ancylostoma", "Ancylostoma infectious disease", "Ancylostoma disease or disorder", "Ancylostoma duodenale infection", "Hookworm infection by Ancylostoma", "infection by Ancylostoma (diagnosis)", "Ancylostoma caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ancylostomiasis", "shortest_name_length": 14}
{"curie": "MONDO:0030922", "names": ["MRD56", "autosomal dominant mental retardation 56", "mental retardation, autosomal dominant 56", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 56", "autosomal dominant intellectual disability 56", "intellectual disability, autosomal dominant 56", "autosomal dominant intellectual developmental disorder 56", "autosomal dominant intellectual developmental disorder-56", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 56"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 56", "shortest_name_length": 5}
{"curie": "UMLS:C5666816", "names": ["MOVLD", "Multiorgan Venous and Lymphatic Defect Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Multiorgan Venous and Lymphatic Defect Syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C2349110", "names": ["vascular access device complications", "Vascular Access Device Complications"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vascular Access Device Complications", "shortest_name_length": 36}
{"curie": "MONDO:0011830", "names": ["ILS", "LIS1", "LISSENCEPHALY 1", "lissencephaly 1", "Lissencephaly 1", "1, Lissencephaly", "Lissencephaly 1s", "1s, Lissencephaly", "Type 1 lissencephaly", "Lissencephaly type 1", "Type 1 Lissencephaly", "Lissencephaly Type 1", "Type I lissencephaly", "Lissencephaly Type I", "Classic lissencephaly", "Type 1, Lissencephaly", "Lissencephaly Type 1s", "1, Lissencephaly Type", "Lissencephaly, Type 1", "Classic Lissencephaly", "Lissencephaly, type I", "Type 1 Lissencephalies", "lissencephaly, classic", "LISSENCEPHALY, CLASSIC", "1s, Lissencephaly Type", "Type 1s, Lissencephaly", "Lissencephaly, Classic", "Lissencephalies, Type 1", "4-layered lissencephaly", "Classical Lissencephaly", "Classic Lissencephalies", "Lissencephaly, Classical", "Lissencephalies, Classic", "Classical Lissencephalies", "Lissencephalies, Classical", "Four-layered lissencephaly", "subcortical band heterotopia", "PAFAH1B1-related lissencephaly", "subcortical laminar heterotopia", "Type 1 lissencephaly (disorder)", "Isolated Lissencephaly Sequence", "Classical Lissencephaly Syndrome", "LISSENCEPHALY SEQUENCE, ISOLATED", "lissencephaly sequence, isolated", "Lissencephaly Sequence, Isolated", "Lissencephaly Syndrome, Classical", "Classical Lissencephaly Syndromes", "Syndrome, Classical Lissencephaly", "Lissencephaly Syndromes, Classical", "lissencephaly due to LIS1 mutation", "Syndromes, Classical Lissencephaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lissencephaly due to LIS1 mutation", "shortest_name_length": 3}
{"curie": "UMLS:C0948689", "names": ["Hepatosplenic candidiasis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatosplenic candidiasis", "shortest_name_length": 25}
{"curie": "MONDO:0003535", "names": ["Fallopian Tube Papillary Adenocarcinoma", "fallopian tube papillary adenocarcinoma", "papillary adenocarcinoma of fallopian tube", "papillary adenocarcinoma of the fallopian tube", "Papillary adenocarcinoma of the fallopian tube", "papillary adenocarcinoma of fallopian tube (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fallopian tube papillary adenocarcinoma", "shortest_name_length": 39}
{"curie": "MONDO:0019231", "names": ["disorder of pentose phosphate metabolism", "inborn disorder of pentose phosphate metabolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of pentose phosphate metabolism", "shortest_name_length": 40}
{"curie": "UMLS:C1336947", "names": ["Vascular Breast Tumor", "Vascular Breast Neoplasm", "Breast Vascular Neoplasm", "Vascular Tumor of Breast", "Vascular Neoplasm of Breast", "Vascular Tumor of the Breast", "Vascular Neoplasm of the Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Vascular Neoplasm", "shortest_name_length": 21}
{"curie": "MONDO:0006839", "names": ["Lutembacher", "Lutembacher syndrome", "Lutembacher Syndrome", "Lutembachers Syndrome", "syndrome, Lutembacher", "Lutembachers syndrome", "Lutembacher's anomaly", "Syndrome, Lutembacher", "Lutembacher's syndrome", "Lutembacher's Syndrome", "syndrome, Lutembacher's", "Syndrome, Lutembacher's", "Lutembacher's syndrome (disorder)", "Lutembacher's syndrome (diagnosis)", "Atrial septal defect and mitral stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lutembacher syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0011648", "names": ["MNRI", "Mnri", "radiation-induced meningioma", "Radiation induced meningioma", "radiation induced meningioma", "Meningioma, Radiation Induced", "meningioma, radiation-induced", "MENINGIOMA, RADIATION-INDUCED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radiation-induced meningioma", "shortest_name_length": 4}
{"curie": "MONDO:0010603", "names": ["HEMOPHILIA A WITH VASCULAR ABNORMALITY", "Hemophilia A with Vascular Abnormality", "hemophilia A with vascular abnormality"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemophilia A with vascular abnormality", "shortest_name_length": 38}
{"curie": "MONDO:0004215", "names": ["anthrax skin", "skin anthrax", "Skin anthrax", "Malignant pustule", "anthrax cutaneous", "Cutaneous anthrax", "CUTANEOUS ANTHRAX", "cutaneous anthrax", "MALIGNANT PUSTULE", "anthrax, skin type", "cutaneous; anthrax", "pustule; malignant", "anthrax; cutaneous", "Anthrax, skin type", "Anthrax, cutaneous", "malignant; pustule", "Cutaneous anthrax (disorder)", "cutaneous anthrax (diagnosis)", "Malignant pustule of skin due to anthrax"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous anthrax", "shortest_name_length": 12}
{"curie": "MONDO:0023171", "names": ["foix chavany Marie syndrome", "anterior opercular syndrome", "Anterior Opercular Syndrome", "Foix Chavany Marie syndrome", "Foix-Chavany-Marie syndrome", "Opercular Syndrome, Anterior", "opercular syndrome, anterior", "Bilateral opercular syndrome", "bilateral anterior opercular syndrome", "Bilateral anterior opercular syndrome", "Pseudobulbar Paralysis, Cortical Type", "pseudobulbar paralysis, cortical type", "Bilateral Anterior Opercular Syndrome", "Foix Chavany Marie syndrome (disorder)", "congenital Foix-Chavany-Marie syndrome", "Congenital Foix-Chavany-Marie syndrome", "facio-pharyngo-glosso-masticatory diplegia", "Facio-pharyngo-glosso-masticatory diplegia", "congenital Foix-Chavany-Marie syndrome (subtype)", "Facio-Labio-Pharyngo-Glosso-Laryngo-Brachial Paralysis", "facio-Labio-pharyngo-Glosso-laryngo-brachial paralysis", "Facio-Pharyngo-Glossal Diplegia with Automatic-Voluntary Movement Dissociation", "Facio-pharyngo-glossal diplegia with automatic-voluntary movement dissociation", "facio-pharyngo-glossal diplegia with automatic-voluntary movement dissociation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "foix chavany Marie syndrome", "shortest_name_length": 27}
{"curie": "MONDO:0030905", "names": ["DFNB117", "DEAFNESS, AUTOSOMAL RECESSIVE 117", "deafness, autosomal recessive 117", "hearing loss, autosomal recessive 117"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal recessive 117", "shortest_name_length": 7}
{"curie": "MONDO:0009867", "names": ["PRKAG2 glycogen storage disease", "Glycogen Storage Disease of Heart", "glycogen storage disease of heart", "GLYCOGEN STORAGE DISEASE OF HEART", "Phosphorylase Kinase Deficiency of Heart", "phosphorylase kinase deficiency of heart", "PHOSPHORYLASE KINASE DEFICIENCY OF HEART", "fatal congenital nonlysosomal cardiac glycogenosis", "lethal congenital glycogen storage disease of heart", "glycogen storage disease of heart, lethal congenital", "Glycogen Storage Disease of Heart, Lethal Congenital", "GLYCOGEN STORAGE DISEASE OF HEART, LETHAL CONGENITAL", "glycogen storage disease caused by mutation in PRKAG2", "fatal congenital hypertrophic cardiomyopathy due to GSD", "Fatal congenital hypertrophic cardiomyopathy due to GSD", "Fatal congenital hypertrophic cardiomyopathy due to glycogenosis", "fatal congenital hypertrophic cardiomyopathy due to glycogenosis", "Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease", "fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease", "Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal congenital glycogen storage disease of heart", "shortest_name_length": 31}
{"curie": "MONDO:0010046", "names": ["SPG23", "SPG 23", "Lison syndrome", "LISON SYNDROME", "Abdallat syndrome", "spastic paraplegia 23", "Spastic paraplegia 23", "Abdallat Davis Farrage syndrome", "hereditary spastic paraplegia 23", "SPASTIC PARAPLEGIA 23 (disorder)", "hereditary spastic paraplegia type 23", "SPASTIC PARAPLEGIA 23, AUTOSOMAL RECESSIVE", "autosomal recessive spastic paraplegia type 23", "Autosomal recessive spastic paraplegia type 23", "Spastic paraplegia and pigmentary abnormalities", "spastic paraplegia and pigmentary abnormalities", "spastic paraplegia with pigmentary abnormalities", "SPASTIC PARAPLEGIA WITH PIGMENTARY ABNORMALITIES", "Spastic Paraplegia With Pigmentary Abnormalities", "DSTYK autosomal recessive complex spastic paraplegia", "familial spastic paraplegia autosomal recessive type 23", "Autosomal recessive spastic paraplegia type 23 (disorder)", "Autosomal recessive spastic paraplegia type 23 (diagnosis)", "SPASTIC PARAPARESIS, VITILIGO, PREMATURE GRAYING, CHARACTERISTIC FACIES", "spastic paraparesis, vitiligo, premature graying, characteristic facies", "Spastic Paraparesis, Vitiligo, Premature Graying, Characteristic Facies", "spastic paraplegia vitiligo premature graying and characteristic facies", "Spastic paraplegia, vitiligo, premature graying and characteristic facies", "autosomal recessive complex spastic paraplegia caused by mutation in DSTYK", "Spastic paraparesis-vitiligo-premature graying-characteristic facies syndrome", "spastic paraparesis-vitiligo-premature graying-characteristic facies syndrome", "Spastic paraparesis, vitiligo, premature graying, characteristic facies syndrome", "Spastic paraparesis, vitiligo, premature greying, characteristic facies syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 23", "shortest_name_length": 5}
{"curie": "UMLS:C0919590", "names": ["Injection site cellulitis", "Cellulitis at injection site", "Cellulitis at injection site (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site cellulitis", "shortest_name_length": 25}
{"curie": "MONDO:0014981", "names": ["IMD49", "IMMUNODEFICIENCY 49", "immunodeficiency 49", "immunodeficiency type 49", "immunodeficiency 49; IMD49", "BCL11B primary immunodeficiency disease", "primary immunodeficiency disease caused by mutation in BCL11B", "SCID, T cell-Negative, B cell-Positive, Nk cell-Positive, with intellectual disability, spasticity, and craniofacial abnormalities", "SCID, T-cell negative, B-cell positive, NK cell positive, with intellectual disability, spasticity, and craniofacial abnormalities", "SCID, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-POSITIVE, WITH INTELLECTUAL DISABILITY, SPASTICITY, AND CRANIOFACIAL ABNORMALITIES", "severe combined immunodeficiency, T cell-Negative, B cell-Positive, Nk cell-Positive, with intellectual disability, spasticity, and craniofacial abnormalities", "severe combined immunodeficiency, T-cell negative, B-cell positive, NK cell positive, with intellectual disability, spasticity, and craniofacial abnormalities", "SEVERE COMBINED IMMUNODEFICIENCY, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-POSITIVE, WITH INTELLECTUAL DISABILITY, SPASTICITY, AND CRANIOFACIAL ABNORMALITIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 49", "shortest_name_length": 5}
{"curie": "MONDO:0003023", "names": ["aorta angiosarcoma", "aortic angiosarcoma", "Aortic Angiosarcoma", "angiosarcoma of aorta", "Angiosarcoma of Aorta", "Aortic hemangiosarcoma", "Aortic Hemangiosarcoma", "aortic hemangiosarcoma", "Hemangiosarcoma of Aorta", "hemangiosarcoma of aorta", "Angiosarcoma of the Aorta", "angiosarcoma of the aorta", "Hemangiosarcoma of the Aorta", "hemangiosarcoma of the aorta", "aorta angiosarcoma (disease)", "angiosarcoma (disease) of aorta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aorta angiosarcoma", "shortest_name_length": 18}
{"curie": "UMLS:C5400232", "names": ["Latent celiac disease", "Microscopic enteritis", "Latent Celiac Disease", "Latent coeliac disease", "Microscopic enteritis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Microscopic enteritis", "shortest_name_length": 21}
{"curie": "UMLS:C4329973", "names": ["Factor XIII Inactivation", "Factor XIII Inhibitor Present"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Factor XIII Inactivation", "shortest_name_length": 24}
{"curie": "UMLS:C0281169", "names": ["pulmonary complication", "PULMONARY COMPLICATION", "Pulmonary Complication", "pulmonary complications", "complications pulmonary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pulmonary Complication", "shortest_name_length": 22}
{"curie": "MONDO:0017923", "names": ["WL syndrome", "facio-audio-symphalangism", "multiple synostoses syndrome", "symphalangism-brachydactyly syndrome", "deafness-Hermann type symphalangism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple synostoses syndrome", "shortest_name_length": 11}
{"curie": "UMLS:C0796621", "names": ["Stage IA Soft Tissue Sarcoma", "stage IA soft tissue sarcoma", "stage IA sarcoma of soft tissue", "Stage IA Sarcoma of Soft Tissue", "stage IA adult soft tissue sarcoma", "stage IA sarcoma of the soft tissue", "Stage IA Sarcoma of the Soft Tissue", "Stage IA Soft Tissue Sarcoma AJCC v7", "stage IA soft tissue sarcoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Soft Tissue Sarcoma AJCC v7", "shortest_name_length": 28}
{"curie": "MONDO:0002258", "names": ["PHARYNGITIS", "Pharyngitis", "sore throat", "Sore Throat", "pharyngitis", "Sore throat", "Pharyngitides", "Inflamed throat", "Pharyngitis NOS", "inflamed throat", "throat soreness", "Inflamed;throat", "soreness throat", "throat inflamed", "inflamed throats", "Pharynx inflamed", "Pharyngitis, NOS", "throat infection", "infection throat", "acute sore throat", "infections throat", "acute pharyngitis", "pharyngeal disease", "Inflammation;throat", "inflammation throat", "Pharyngitis - acute", "throat inflammation", "Pharyngeal disorder", "chronic pharyngitis", "pharyngeal disorder", "chronic sore throat", "pharyngitis - acute", "pharynx inflammation", "inflammation; throat", "throat; inflammation", "pharynx; inflammation", "inflammation; pharynx", "Sore throat - chronic", "persistent sore throat", "Persistent sore throat", "inflammation of throat", "Pharyngitis (disorder)", "PHARYNGEAL INFLAMMATION", "inflammation of pharynx", "Pharyngeal inflammation", "pharyngitis (diagnosis)", "pharyngeal inflammation", "irritation of the throat", "inflammation of the throat", "chronic pharyn/nasopharyngitis", "chronic pharyngitis and nasopharyngitis", "Chronic pharyngitis and nasopharyngitis", "inflammation of pharynx (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pharyngitis", "shortest_name_length": 11}
{"curie": "MONDO:0009356", "names": ["humeroradial synostosis", "humeroradial/multiple synostosis syndrome", "HUMERORADIAL/MULTIPLE SYNOSTOSIS SYNDROME", "Humeroradial Multiple Synostosis Syndrome", "autosomal recessive humeroradial synostosis", "autosomal recessive humeroradial synostosis (disease)", "humeroradial synostosis (disease), autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive humeroradial synostosis", "shortest_name_length": 23}
{"curie": "UMLS:C4551756", "names": ["Refractory Waldenstrom Macroglobulinemia", "Waldenstrom's macroglobulinemia refractory", "Waldenstrom's macroglobulinaemia refractory"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Waldenstrom's macroglobulinemia refractory", "shortest_name_length": 40}
{"curie": "MONDO:0009049", "names": ["MMAD", "AIMAH", "ACTH-independent Cushing syndrome", "primary macronodular adrenal hyperplasia", "massive macronodular adrenocortical disease", "Acth-Independent Macronodular Adrenal Hyperplasia", "ACTH-independent macronodular adrenal hyperplasia", "Primary bilateral macronodular adrenal hyperplasia", "primary bilateral macronodular adrenal hyperplasia", "Cushing syndrome due to macronodular adrenal hyperplasia", "Hypercortisolism due to macronodular adrenal hyperplasia", "ACTH-independent macronodular adrenocortical hyperplasia", "Cushing's syndrome due to adrenal macronodular hyperplasia", "corticotropin-independent macronodular adrenal hyperplasia", "Hypercortisolism due to macronodular adrenal hyperplasia (disorder)", "Cushing's syndrome due to adrenal macronodular hyperplasia (diagnosis)", "adrenocorticotropic hormone-independent macronodular adrenal hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cushing syndrome due to macronodular adrenal hyperplasia", "shortest_name_length": 4}
{"curie": "UMLS:C0162442", "names": ["parapsoriasis en plaque", "Parapsoriasis en Plaque", "Parapsoriasis en plaque", "Parapsoriasis en Plaques", "Parapsoriasis en plaques", "parapsoriasis en plaques", "parapsoriasis large plaque", "Large Plaque Parapsoriasis", "large plaque parapsoriasis", "Large plaque parapsoriasis", "parapsoriasis; large plaque", "large plaque; parapsoriasis", "Plaque-type premycotic eruption", "Parapsoriasis en plaques (disorder)", "Large plaque parapsoriasis (disorder)", "large plaque parapsoriasis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parapsoriasis en Plaques", "shortest_name_length": 23}
{"curie": "UMLS:C5239573", "names": ["Unresectable Fibrosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Fibrosarcoma", "shortest_name_length": 25}
{"curie": "MONDO:0006011", "names": ["VIRUS HEPATITIS", "VIRAL HEPATITIS", "Viral hepatitis", "viral Hepatitis", "virus hepatitis", "HEPATITIS VIRAL", "Hepatitis;viral", "Virus hepatitis", "Hepatitis viral", "Viral Hepatitis", "hepatitis viral", "viral hepatitis", "virus; hepatitis", "hepatitis; virus", "Viruses hepatitis", "Hepatitis viral NOS", "Viral hepatitis NOS", "VH - Viral hepatitis", "Viral hepatitis, NOS", "viral human hepatitis", "Human Viral Hepatitis", "human viral hepatitis", "animal viral hepatitis", "Viral Hepatitis, Human", "Human Viral Hepatitides", "Hepatitis, Viral, Human", "Hepatic viral infections", "Viruses caused hepatitis", "Viral Hepatitides, Human", "Viral hepatitis (B15-B19)", "Viral hepatitis (disorder)", "Unspecified viral hepatitis", "viral hepatitis (diagnosis)", "viral human hepatitis infection", "Viral hepatitis with hepatic coma", "viral hepatitis with hepatic coma", "infectious hepatitis (viral hepatitis)", "unspecified viral hepatitis with hepatic coma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "viral hepatitis", "shortest_name_length": 15}
{"curie": "MONDO:0007462", "names": ["MS", "disseminated sclerosis", "multiple sclerosis, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple sclerosis, susceptibility to", "shortest_name_length": 2}
{"curie": "MONDO:0000226", "names": ["mineral metabolism disease", "Mineral metabolism disorder", "mineral metabolism disorder", "mineral; metabolic disorder", "metabolic disorder; mineral", "disease of mineral metabolism", "disorder of mineral metabolism", "Disorder of mineral metabolism", "disorders of mineral metabolism", "Disorders of mineral metabolism", "DISORDERS OF MINERAL METABOLISM", "Mineral metabolism disorder NOS", "Disorder of mineral metabolism, NOS", "mineral metabolism disorder (diagnosis)", "Disorder of mineral metabolism (disorder)", "Unspecified disorder of mineral metabolism", "Disorder of mineral metabolism, unspecified", "DISORDERS OF MINERAL METABOLISM: GENERAL TERMS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mineral metabolism disease", "shortest_name_length": 26}
{"curie": "UMLS:C5420155", "names": ["Hairy Polyp", "Dermoid Polyp", "Teratoid Polyp"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hairy Polyp", "shortest_name_length": 11}
{"curie": "UMLS:C0027019", "names": ["leukemia myelomonocytic", "Myelomonocytic leukemia", "myelomonocytic leukemia", "leukemia; myelomonocytic", "myelomonocytic; leukemia", "Myelomonocytic leukaemia", "Myelomonocytic leukemia, NOS", "Myelomonocytic leukaemia, NOS", "Myelomonocytic leukemia (disorder)", "Myelomonocytic leukemia (diagnosis)", "Myelomonocytic leukemia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myelomonocytic leukemia", "shortest_name_length": 23}
{"curie": "MONDO:0017164", "names": ["anti-K HDN", "maternal anti-Kell alloimmunization", "hemolytic disease of the newborn with Kell alloimmunization"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemolytic disease of the newborn with Kell alloimmunization", "shortest_name_length": 10}
{"curie": "UMLS:C4525696", "names": ["Stage IV Appendix Neuroendocrine Tumor", "Stage IV Appendix Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Appendix Neuroendocrine Tumor AJCC v8", "shortest_name_length": 38}
{"curie": "UMLS:C5239068", "names": ["Advanced Malignant Peripheral Nerve Sheath Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Malignant Peripheral Nerve Sheath Tumor", "shortest_name_length": 48}
{"curie": "UMLS:C2981374", "names": ["Stage IIIC Esophageal Adenocarcinoma", "Stage IIIC Esophageal Adenocarcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Esophageal Adenocarcinoma AJCC v7", "shortest_name_length": 36}
{"curie": "MONDO:0007943", "names": ["AFD", "NAFD", "AFD1", "Afd1", "Nager anomaly", "nager syndrome", "NAGER SYNDROME", "Nager syndrome", "syndrome nager", "AFD, NAGER TYPE", "AFD, Nager type", "Preaxial acrodysostosis", "preaxial acrodysostosis", "Nager-de Reynier syndrome", "Nager syndrome (disorder)", "nager acrofacial dysostosis", "Nager Acrofacial Dysostosis", "Nager acrofacial dysostosis", "NAGER ACROFACIAL DYSOSTOSIS", "Preaxial acrofacial dysostosis", "preaxial acrofacial dysostosis", "Acrofacial dysostosis, Nager type", "preaxial manibulofacial dysostosis", "acrofacial dysostosis 1, Nager type", "ACROFACIAL DYSOSTOSIS 1, NAGER TYPE", "preaxial mandibulofacial dysostosis", "Acrofacial Dysostosis 1, Nager Type", "Preaxial Mandibulofacial Dysostosis", "Nager Acrofacial Dysostosis Syndrome", "Nager acrofacial dysostosis syndrome", "split hand deformity-mandibulofacial dysostosis", "mandibulofacial dysostosis with preaxial limb anomalies", "Mandibulofacial dysostosis with preaxial limb anomalies", "mandibulofacial dysostosis with limb malformations syndrome", "MANDIBULOFACIAL DYSOSTOSIS, TREACHER COLLINS TYPE, WITH LIMB ANOMALIES", "Mandibulofacial dysostosis, Treacher Collins type, with limb anomalies", "mandibulofacial dysostosis, Treacher Collins type, with limb anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nager acrofacial dysostosis", "shortest_name_length": 3}
{"curie": "MONDO:0019907", "names": ["R13", "Ring 13", "r(13) syndrome", "(13)r syndrome", "ring chromosome 13", "chromosome 13 ring", "Ring chromosome 13", "Chromosome 13 ring", "Ring chromosome type 13", "Ring chromosome 13 syndrome", "Ring Chromosome 13 Syndrome", "ring chromosome 13 syndrome", "chromosome 13 ring syndrome", "Ring chromosome 13 syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ring chromosome 13", "shortest_name_length": 3}
{"curie": "MONDO:0032772", "names": ["BANDDOS", "brain abnormalities, neurodegeneration, and dysosteosclerosis", "BRAIN ABNORMALITIES, NEURODEGENERATION, AND DYSOSTEOSCLEROSIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brain abnormalities, neurodegeneration, and dysosteosclerosis", "shortest_name_length": 7}
{"curie": "MONDO:0016159", "names": ["Gemignani syndrome", "Gemignani syndrome (disorder)", "spinocerebellar ataxia-amyotrophy-deafness syndrome", "Spinocerebellar ataxia-amyotrophy-deafness syndrome", "Spinocerebellar ataxia, amyotrophy, deafness syndrome", "Spinocerebellar ataxia-amyotrophy-hearing loss syndrome", "spinocerebellar ataxia associated amyotrophy of the hands and sensorineural deafness", "Spinocerebellar ataxia associated with localized amyotrophy of the hands, sensorineural deafness and spastic paraparesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gemignani syndrome", "shortest_name_length": 18}
{"curie": "MONDO:0005164", "names": ["Fibrosarcoma", "fibrosarcoma", "FIBROSARCOMA", "Fibrosarcomas", "fibrosarcomas", "Fibrocytic tumor", "Fibrosarcoma NOS", "fibrocytic tumor", "Fibrosarcoma, NOS", "[M]Fibrosarcoma NOS", "fibrosarcoma (disease)", "FIBROSARCOMA, MALIGNANT", "Fibrosarcoma (disorder)", "Fibrosarcomas malignant", "fibrous tissue neoplasm", "fibrosarcoma, malignant", "Soft Tissue Fibrosarcoma", "fibrosarcoma (diagnosis)", "Fibrosarcoma of Soft Tissue", "fibrosarcoma of soft tissue", "fibrosarcoma - not infantile", "malignant neoplasm fibromatous", "Malignant Fibromatous Neoplasm", "Malignant fibromatous neoplasm", "malignant fibromatous neoplasm", "Fibrosarcoma of the Soft Tissue", "Fibrosarcoma (morphologic abnormality)", "fibrosarcoma of soft tissue (diagnosis)", "Malignant fibromatous neoplasm (disorder)", "malignant fibromatous neoplasm (diagnosis)", "fibrosarcoma (excluding infantile fibrosarcoma)", "Malignant fibromatous neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibrosarcoma", "shortest_name_length": 12}
{"curie": "MONDO:0020522", "names": ["EDS7B", "EDS VIIB", "EDSARTH2", "Ehlers-Danlos syndrome type 7B", "Ehlers-Danlos syndrome, arthrochalasia type, 2", "EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2", "EHLERS-DANLOS SYNDROME, TYPE VIIB, AUTOSOMAL DOMINANT", "Ehlers-Danlos syndrome, type VIIB, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ehlers-Danlos syndrome type 7B", "shortest_name_length": 5}
{"curie": "MONDO:0020369", "names": ["Chandler syndrome", "chandler syndrome", "Chandler Syndrome", "chandlers syndrome", "Chandlers Syndrome", "Chandler's syndrome", "Chandler's Syndrome", "chandler's syndrome", "Chandler syndrome (disorder)", "Endothelial corneal dystrophy", "endothelial corneal dystrophy", "Chandler's syndrome (diagnosis)", "dystrophy of corneal endothelium", "Dystrophy of corneal endothelium", "posterior membrane corneal dystrophy", "Posterior membrane corneal dystrophy", "Corneal dystrophy, edema, glaucoma syndrome", "Iris Atrophy with Corneal Edema and Glaucoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chandler syndrome", "shortest_name_length": 17}
{"curie": "MONDO:0025369", "names": ["Nairobi", "sheep virus (Nairobi)", "Nairobi sheep disease", "Nairobi Sheep Disease", "disease, Nairobi sheep", "sheep disease, Nairobi", "Sheep Disease, Nairobi", "Disease, Nairobi Sheep", "Nairobi sheep virus disease", "Nairobi sheep disease (diagnosis)", "Nairobi sheep virus disease (disorder)", "disease (or disorder); Nairobi (sheep virus)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nairobi sheep disease", "shortest_name_length": 7}
{"curie": "UMLS:C4076686", "names": ["Supine hypertension", "Supine hypertension (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Supine hypertension", "shortest_name_length": 19}
{"curie": "UMLS:C0750053", "names": ["Vaginal Abscess", "Vaginal abscess", "vagina; abscess", "VAGINAL ABSCESS", "vaginal abscess", "abscess; vagina"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal abscess", "shortest_name_length": 15}
{"curie": "UMLS:C5418959", "names": ["Refractory Primary Peritoneal Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Primary Peritoneal Serous Adenocarcinoma", "shortest_name_length": 51}
{"curie": "MONDO:0016612", "names": ["X-linked hereditary ataxia", "X-linked cerebellar ataxia", "cerebellar ataxia, X-linked", "hereditary ataxia, X-linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked cerebellar ataxia", "shortest_name_length": 26}
{"curie": "MONDO:0010956", "names": ["Seow Najjar syndrome", "enamel hypoplasia, cataracts, and aqueductal stenosis", "ENAMEL HYPOPLASIA, CATARACTS, AND AQUEDUCTAL STENOSIS", "Enamel Hypoplasia, Cataracts, and Aqueductal Stenosis", "enamel hypoplasia, capsular cataracts, and ductal stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "enamel hypoplasia, cataracts, and aqueductal stenosis", "shortest_name_length": 20}
{"curie": "MONDO:0005723", "names": ["MENINGITIS TORULA", "crypto meningitis", "Meningitis torula", "Cryptococcal Meningitis", "MENINGITIS CRYPTOCOCCAL", "CRYPTOCOCCAL MENINGITIS", "cryptococcal meningitis", "Cryptococcal meningitis", "Meningitis cryptococcal", "meningitis cryptococcal", "Meningitis, Cryptococcal", "Cryptococcal Meningitides", "Meningitides, Cryptococcal", "Meningitis due to cryptococcus", "Meningitis due to Cryptococcus", "Cryptococcus neoformans meningitis", "Cryptococcal meningitis (disorder)", "cryptococcal meningitis (diagnosis)", "Cryptococcus neoformans infectious meningitis", "Cryptococcus neoformans caused infectious meningitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cryptococcal meningitis", "shortest_name_length": 17}
{"curie": "MONDO:0010148", "names": ["TRACHEOBRONCHOMEGALY", "Tracheobronchomegaly", "tracheobronchomegaly", "mounier-kuhn syndrome", "Mounier-Kühn syndrome", "Mounier-Kuhn Syndrome", "Mounier Kuhn syndrome", "Mounier Kuhn Syndrome", "Mounier-Kuhn syndrome", "mounier kuhn syndrome", "Tracheobronchomegalies", "Idiopathic tracheobronchomegaly", "Congenital Tracheobronchomegaly", "congenital tracheobronchomegaly", "Congenital tracheobronchomegaly", "idiopathic tracheobronchomegaly", "Congenital tracheobronchiomegaly", "Tracheobronchomegaly, Congenital", "Congenital Tracheobronchomegalies", "Tracheobronchomegalies, Congenital", "Congenital tracheobronchomegaly (disorder)", "congenital tracheobronchomegaly (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mounier-Kuhn syndrome", "shortest_name_length": 20}
{"curie": "UMLS:C0338489", "names": ["Status migrainus", "status migrainus", "migraine; status", "status; migraine", "Status Migranosus", "Status Migrainosus", "Status migrainosus", "status migrainosus", "migrainosus; status", "status; migrainosus", "Status migrainosus NOS", "Status migrainosus (disorder)", "status migrainosus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Status Migrainosus", "shortest_name_length": 16}
{"curie": "MONDO:0044355", "names": ["isolated SCCH", "Isolated SCCH", "Sternocostoclavicular Hyperostosis", "Sternocostoclavicular Hyperostoses", "Hyperostosis, Sternocostoclavicular", "Hyperostoses, Sternocostoclavicular", "isolated sternocostoclavicular hyperostosis", "Isolated sternocostoclavicular hyperostosis", "Isolated SCCH (sternocostoclavicular hyperostosis)", "Isolated sternocostoclavicular hyperostosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated sternocostoclavicular hyperostosis", "shortest_name_length": 13}
{"curie": "UMLS:C5446431", "names": ["Malignant Lacrimal Drainage System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Lacrimal Drainage System Neoplasm", "shortest_name_length": 43}
{"curie": "UMLS:C1167785", "names": ["Hemorrhagic urticaria", "Urticaria hemorrhagica", "Haemorrhagic urticaria", "Urticaria haemorrhagica"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemorrhagic urticaria", "shortest_name_length": 21}
{"curie": "UMLS:C2004493", "names": ["B Cell Leukemia", "B-Cell Leukemia", "Leukemia, B Cell", "B-Cell Leukemias", "Leukemia, B-Cell", "Leukemias, B-Cell", "B Lymphocytic Leukemia", "B-Lymphocytic Leukemia", "B-Lymphocytic Leukemias", "Leukemia, B-Lymphocytic", "Leukemias, B-Lymphocytic", "B-Cell Lymphocytic Leukemia", "Leukemia, B-Cell Lymphocytic", "Lymphocytic Leukemia, B-Cell", "Lymphocytic Leukemia, B Cell", "B-Cell Lymphocytic Leukemias", "Leukemia, Lymphocytic, B Cell", "Leukemia, Lymphocytic, B-Cell", "Lymphocytic Leukemias, B-Cell", "Leukemias, B-Cell Lymphocytic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leukemia, B-Cell", "shortest_name_length": 15}
{"curie": "UMLS:C1335321", "names": ["Papillary Breast Tumor", "Papillary Tumor of Breast", "Papillary Breast Neoplasm", "Breast Papillary Neoplasm", "Papillary Neoplasm of Breast", "Papillary Tumor of the Breast", "Papillary Neoplasm of the Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Papillary Neoplasm", "shortest_name_length": 22}
{"curie": "UMLS:C0475735", "names": ["Intraventricular Hemorrhage of Prematurity", "Intraventricular hemorrhage of prematurity", "Intraventricular haemorrhage of prematurity", "Intraventricular hemorrhage of prematurity (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraventricular hemorrhage of prematurity", "shortest_name_length": 42}
{"curie": "UMLS:C4763838", "names": ["Metastatic Small Cell Prostate Cancer", "Metastatic Prostate Small Cell Carcinoma", "Metastatic Small Cell Neuroendocrine Prostate Cancer", "Metastatic Prostate Small Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Prostate Small Cell Neuroendocrine Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0021063", "names": ["ca colon", "colon ca", "Colon Cancer", "COLON CANCER", "Colon cancer", "colon cancer", "colon cancers", "Cancer, Colon", "Colon Cancers", "cancer colons", "Colonic cancer", "cancer colonic", "Cancers, Colon", "colonic cancer", "Colonic Cancer", "of cancer colon", "Cancer of colon", "Colonic Cancers", "Cancer of Colon", "Cancer, Colonic", "cancer of colon", "COLON NOS CANCER", "Cancers, Colonic", "Colon cancer NOS", "Colonic cancer NOS", "of the colon cancer", "cancer of the colon", "Cancer of the Colon", "CA - Cancer of colon", "Malignant Colon Tumor", "malignant colon tumor", "Colon Tumor, Malignant", "colon tumor, malignant", "Malignant colonic tumor", "malignant colonic tumor", "Malignant Colonic Tumor", "malignant tumor of colon", "malignant colon neoplasm", "Malignant tumor of colon", "Malignant Tumor of Colon", "Malignant Colon Neoplasm", "Malignant tumour of colon", "colon neoplasm, malignant", "Colon Neoplasm, Malignant", "malignant colonic neoplasm", "Malignant Colonic Neoplasm", "Malignant Neoplasm of Colon", "malignant neoplasm of colon", "Malignant neoplasm of colon", "Malignant Tumor of the Colon", "malignant tumor of the colon", "malignant neoplasm of the colon", "Malignant Neoplasm of the Colon", "Malignant neoplasm of colon, NOS", "Malignant neoplasm of colon (disorder)", "Malignant neoplasm of colon (diagnosis)", "Malignant neoplasm of colon, unspecified", "Malignant neoplasm of colon, unspecified site", "Malignant neoplasm of colon, unspecified part"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant colon neoplasm", "shortest_name_length": 8}
{"curie": "MONDO:0011264", "names": ["DYT6", "DYT-THAP1", "Dystonia 6", "dystonia 6", "THAP1 dystonia", "Torsion dystonia 6", "torsion dystonia 6", "Torsion Dystonia 6", "dystonia 6, torsion", "DYSTONIA 6, TORSION", "Dystonia 6, torsion", "Dystonia 6 (disorder)", "torsion dystonia type 6", "primary dystonia, DYT6 type", "Primary dystonia, DYT6 type", "THAP1 generalized isolated dystonia", "adolescent-onset dystonia of mixed type", "Torsion dystonia adult onset mixed type", "torsion dystonia adult onset mixed type", "idiopathic torsion dystonia of mixed type", "TORSION DYSTONIA, ADULT-ONSET, MIXED TYPE", "Idiopathic torsion dystonia of mixed type", "torsion dystonia, adult-onset, mixed type", "Torsion Dystonia, Adult-Onset, Mixed Type", "generalized cervical and upper-limb-onset dystonia", "Generalized cervical and upper-limb-onset dystonia", "generalized isolated dystonia caused by mutation in THAP1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "torsion dystonia 6", "shortest_name_length": 4}
{"curie": "UMLS:C2204420", "names": ["Tongue Adenosquamous Carcinoma", "adenosquamous carcinoma of tongue", "adenosquamous carcinoma of tongue (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenosquamous carcinoma of tongue", "shortest_name_length": 30}
{"curie": "MONDO:0010363", "names": ["MRX91", "XLID91", "X-linked mental retardation 91", "MENTAL RETARDATION, X-LINKED 91", "mental retardation, X-linked 91", "Mental Retardation, X-Linked 91", "mental retardation, X-linked type 91", "intellectual disability, X-linked 91", "intellectual disability, X-linked type 91", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 91", "non-syndromic X-linked intellectual disability 91", "mental retardation, X-linked 91, X-linked dominant", "ZDHHC15 non-syndromic X-linked intellectual disability", "non-syndromic X-linked intellectual disability caused by mutation in ZDHHC15"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 91", "shortest_name_length": 5}
{"curie": "UMLS:C4553582", "names": ["Stage III Vaginal Cancer", "Stage III Vaginal Cancer AJCC v8", "Stage III Vaginal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Vaginal Cancer AJCC v8", "shortest_name_length": 24}
{"curie": "MONDO:0019482", "names": ["dendritic cell sarcoma not otherwise specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dendritic cell sarcoma not otherwise specified", "shortest_name_length": 46}
{"curie": "MONDO:0024467", "names": ["apocrine sweat gland disease", "apocrine sweat gland disorder", "disease of apocrine sweat gland", "disorder of apocrine sweat gland", "apocrine sweat gland disease or disorder", "disease or disorder of apocrine sweat gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "apocrine sweat gland disorder", "shortest_name_length": 28}
{"curie": "MONDO:0014701", "names": ["SEDSTN", "SED Stanescu type", "SED, STANESCU TYPE", "SED, Stanescu type", "spondyloepiphyseal dysplasia Stanescu type", "Spondyloepiphyseal dysplasia Stanescu type", "Spondyloepiphyseal dysplasia, Stanescu type", "spondyloepiphyseal dysplasia, Stanescu type", "SPONDYLOEPIPHYSEAL DYSPLASIA, STANESCU TYPE", "SED (spondyloepiphyseal dysplasia) Stanescu type", "Spondyloepiphyseal dysplasia Stanescu type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepiphyseal dysplasia, Stanescu type", "shortest_name_length": 6}
{"curie": "MONDO:0005661", "names": ["babesiosis", "Babesioses", "BABESIASIS", "babesiasis", "Babesiases", "Babesiosis", "Babesiasis", "BABESIOSIS", "Texas fever", "Piroplasmosis", "piroplasmosis", "PIROPLASMOSIS", "Piroplasmoses", "REDWATER FEVER", "Red water fever", "Human babesiosis", "babesia infection", "Bovine babesiosis", "Babesia Infection", "Babesia infection", "Bovine tick fever", "infection; Babesia", "Babesia; infection", "Infection, Babesia", "Babesia Infections", "Babesia infections", "Infections, Babesia", "Infection by babesia", "infection by Babesia", "Infection by Babesia", "infection; Piroplasma", "Piroplasma; infection", "Babesiosis (disorder)", "babesiosis (diagnosis)", "Babesiosis, unspecified", "Infection by Babesia, NOS", "Piroplasmosis, unspecified", "Babesia infectious disease", "Babesia parasite infection", "Babesia Parasite Infection", "Babesia Parasite Infections", "Infection, Babesia Parasite", "Babesia disease or disorder", "Infections, Babesia Parasite", "Infection by Babesia bigemina", "Babesia caused disease or disorder", "Infection by Babesia bigemina (disorder)", "Babesiosis due to unspecified Babesia species"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "babesiosis", "shortest_name_length": 10}
{"curie": "UMLS:C4086167", "names": ["Childhood Ovarian Mixed Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Ovarian Mixed Germ Cell Tumor", "shortest_name_length": 39}
{"curie": "MONDO:0012609", "names": ["Ad12", "AD12", "Alzheimer Disease 12", "Alzheimer disease 12", "ALZHEIMER DISEASE 12", "Alzheimer's disease 12", "Alzheimer disease type 12", "Alzheimer's disease type 12", "Alzheimer disease familial 12", "Alzheimer disease, familial, 12", "ALZHEIMER DISEASE, FAMILIAL, 12", "Alzheimer Disease, Familial, 12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alzheimer disease 12", "shortest_name_length": 4}
{"curie": "UMLS:C5420440", "names": ["Maxillofacial Osteoblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Maxillofacial Osteoblastoma", "shortest_name_length": 27}
{"curie": "MONDO:0018273", "names": ["XYLT18-CDG", "XYLT1-congenital disorder of glycosylation", "XYLT1-CDG - xylosyltransferase 1 congenital disorder of glycosylation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "XYLT1-congenital disorder of glycosylation", "shortest_name_length": 10}
{"curie": "MONDO:0006073", "names": ["Adenoameloblastoma", "adenoameloblastoma", "Adenomatoid ameloblastoma", "adenomatoid odontogenic tumor", "Adenomatoid odontogenic tumor", "Adenomatoid Odontogenic Tumor", "Pleomorphic adenomatoid tumor", "Adenomatoid odontogenic tumour", "adenomatoid; odontogenic tumor", "odontogenic; tumor, adenomatoid", "tumor; odontogenic, adenomatoid", "adenomatoid; tumor, odontogenic", "tumor; adenomatoid, odontogenic", "adenomatoid odontogenic neoplasm", "Adenomatoid Odontogenic Neoplasm", "Adenomatoid odontogenic tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenomatoid odontogenic tumor", "shortest_name_length": 18}
{"curie": "MONDO:0012904", "names": ["Epm1b", "EPM1B", "Pme with Ataxia", "Progressive Myoclonic Epilepsy 1b", "Progressive myoclonic epilepsy 1B", "progressive myoclonus epilepsy 1B", "epilepsy, progressive myoclonic 1B", "Epilepsy, Progressive Myoclonic, 1b", "epilepsy, progressive myoclonic, 1B", "EPILEPSY, PROGRESSIVE MYOCLONIC, 1B", "PRICKLE1 progressive myoclonic epilepsy", "epilepsy, progressive myoclonic, type 1B", "progressive myoclonic epilepsy with ataxia", "Progressive myoclonus epilepsy with ataxia", "Progressive Myoclonus Epilepsy with Ataxia", "Progressive myoclonus epilepsy with ataxia (disorder)", "progressive myoclonic epilepsy with ataxia (diagnosis)", "PRICKLE1-related progressive myoclonic epilepsy with ataxia", "Prickle1-Related Progressive Myoclonic Epilepsy with Ataxia", "Prickle1-Related Progressive Myoclonus Epilepsy with Ataxia", "progressive myoclonic epilepsy caused by mutation in PRICKLE1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, progressive myoclonic, 1B", "shortest_name_length": 5}
{"curie": "MONDO:0036591", "names": ["adrenocortical tumor", "adrenal cortex tumor", "Adrenal Cortex Tumor", "Adrenocortical Tumor", "adrenal cortex tumors", "Adrenal cortical tumor", "Adrenal cortex--Tumors", "tumor of adrenal cortex", "adrenal cortex neoplasm", "tumor; adrenal cortical", "Adrenal Cortex Neoplasm", "Adrenocortical Neoplasm", "Tumor of adrenal cortex", "adrenal cortical; tumor", "adrenocortical neoplasm", "adrenal; cortical, tumor", "adrenal; tumor, cortical", "Neoplasm, Adrenal Cortex", "Adrenal Cortex Neoplasms", "Tumour of adrenal cortex", "adrenal cortex neoplasms", "Adrenal Cortical Neoplasm", "Neoplasms, Adrenal Cortex", "neoplasm of adrenal cortex", "Cortical adrenal neoplasia", "Neoplasm of adrenal cortex", "Adrenal cortical tumor, NOS", "Adrenal cortical tumour, NOS", "Neoplasm of the adrenal cortex", "Neoplasm of adrenal cortex (disorder)", "neoplasm of adrenal cortex (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adrenal cortex neoplasm", "shortest_name_length": 20}
{"curie": "MONDO:0009787", "names": ["MGA3", "MGCA3", "OPA3 defect", "MGA, type 3", "MGA type III", "MGA, TYPE III", "COSTEFF SYNDROME", "Costeff syndrome", "OPA3, autosomal recessive", "OPA3, AUTOSOMAL RECESSIVE", "OPA3, Autosomal Recessive", "optic atrophy plus syndrome", "OPTIC ATROPHY PLUS SYNDROME", "Optic atrophy plus syndrome", "Costeff optic atrophy syndrome", "Iraqi Jewish optic atrophy plus", "Iraqi-Jewish optic atrophy plus", "OPA3 3-methylglutaconic aciduria", "Iraqi-Jewish 'optic atrophy plus'", "IRAQI-JEWISH 'OPTIC ATROPHY PLUS'", "3-methylglutaconic aciduria type 3", "3-Methylglutaconic aciduria type 3", "3-methylglutaconic aciduria, type 3", "3-methylglutaconic aciduria type III", "Optic Atrophy 3, Autosomal Recessive", "optic atrophy 3, autosomal recessive", "OPTIC ATROPHY 3, AUTOSOMAL RECESSIVE", "3-METHYLGLUTACONIC ACIDURIA, TYPE III", "3-methylglutaconic aciduria, type III", "3-@METHYLGLUTACONIC ACIDURIA, TYPE III", "autosomal recessive optic atrophy type 3", "Autosomal recessive optic atrophy type 3", "3-alpha methylglutaconic aciduria type III", "3-Methylglutaconic aciduria type 3 (disorder)", "autosomal recessive optic atrophy plus syndrome", "Autosomal recessive optic atrophy plus syndrome", "3-methylglutaconic aciduria caused by mutation in OPA3", "Infantile optic atrophy with chorea and spastic paraplegia", "infantile optic atrophy with chorea and spastic paraplegia", "optic atrophy infantile with chorea and spastic paraplegia", "Optic atrophy, infantile, with chorea and spastic paraplegia", "optic atrophy, infantile, with chorea and spastic paraplegia", "OPTIC ATROPHY, INFANTILE, WITH CHOREA AND SPASTIC PARAPLEGIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "3-methylglutaconic aciduria type 3", "shortest_name_length": 4}
{"curie": "MONDO:0012913", "names": ["WAGRO", "Wagro syndrome", "WAGRO SYNDROME", "WAGRO Syndrome", "WAGR Syndrome With Obesity", "WAGR SYNDROME WITH OBESITY", "WAGR syndrome with obesity", "CHROMOSOME 11p13-p12 DELETION SYNDROME", "chromosome 11P13-p12 deletion syndrome", "Chromosome 11p13-P12 Deletion Syndrome", "Wilms tumor-aniridia-genitourinary anomalies-mental retardation-obesity syndrome", "Wilms Tumor-Aniridia-Genitourinary Anomalies-Mental Retardation-Obesity Syndrome", "Wilms tumor-aniridia-genitourinary anomalies-intellectual disability-obesity syndrome", "WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, MENTAL RETARDATION, AND OBESITY SYNDROME", "Wilms tumor, aniridia, genitourinary anomalies, mental retardation, and obesity syndrome", "Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome", "Wilms tumor, aniridia, genitourinary anomalies, intellectual disability, and obesity syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wilms tumor, aniridia, genitourinary anomalies, intellectual disability, and obesity syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C1335499", "names": ["PD", "Disease Progression", "Progressive disease", "Progressive Disease", "PROGRESSIVE DISEASE", "PD-Progressive Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Progressive Disease", "shortest_name_length": 2}
{"curie": "UMLS:C4527170", "names": ["Stage III Cutaneous (Skin) Melanoma", "Clinical Stage III Cutaneous Melanoma AJCC v8", "Clinical Stage III Melanoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage III Cutaneous Melanoma AJCC v8", "shortest_name_length": 35}
{"curie": "UMLS:C4331232", "names": ["Recurrent Secondary Malignancy", "Recurrent Subsequent Malignancy", "Recurrent Secondary Malignant Neoplasm", "Recurrent Subsequent Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Subsequent Malignant Neoplasm", "shortest_name_length": 30}
{"curie": "MONDO:0019609", "names": ["ZS", "ZWS", "CHR", "Zellweger", "Severe PBD-ZSD", "Pipecolicacidemia", "zellweger disease", "Zellweger Disease", "Zellweger syndrome", "Zellweger Syndrome", "Hyperpipecolatemia", "syndrome zellweger", "Pipecolic acidemia", "Pipecolic Acidemia", "pipecolic acidemia", "zellweger syndrome", "Pipecolic acidaemia", "zellwegers syndrome", "Zellweger's syndrome", "zellweger's syndrome", "Zellweger's Syndrome", "Hyperpipecolic acidemia", "Hyperpipecolic Acidemia", "Hyperpipecolic acidaemia", "congenital iron overload", "Acidemia, Hyperpipecolic", "Hyperpipecolic Acidemias", "Zellweger leukodystrophy", "Acidemias, Hyperpipecolic", "CEREBROHEPATORENAL SYNDROME", "Cerebrohepatorenal syndrome", "Cerebrohepatorenal Syndrome", "cerebrohepatorenal syndrome", "Zellweger spectrum disorders", "Cerebro Hepato Renal Syndrome", "Cerebro-Hepato-Renal Syndrome", "Zellweger syndrome (disorder)", "Pipecolic acidemia (disorder)", "pipecolic acidemia (diagnosis)", "Zellweger syndrome (diagnosis)", "Severe peroxisome biogenesis disorder-Zellweger spectrum disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Zellweger spectrum disorders", "shortest_name_length": 2}
{"curie": "UMLS:C4524642", "names": ["Esophageal Adenocarcinoma by AJCC v8 ypTNM Stage", "Esophageal Adenocarcinoma by AJCC v8 Postneoadjuvant Therapy Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Adenocarcinoma by AJCC v8 Postneoadjuvant Therapy Stage", "shortest_name_length": 48}
{"curie": "UMLS:C1336364", "names": ["stage IVB endometrial cancer", "stage IVB uterine corpus cancer", "stage IVB endometrial carcinoma", "Stage IVB Uterine Corpus Cancer", "stage IVB uterine corpus cancer AJCC v7", "Stage IVB Uterine Corpus Cancer AJCC v7", "Stage IVB Uterine (including Endometrial) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Uterine Corpus Cancer AJCC v7", "shortest_name_length": 28}
{"curie": "MONDO:0014171", "names": ["CDCBM4", "complex cortical dysplasia with other brain malformations 4", "cortical dysplasia, complex, with other brain malformations 4", "CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 4", "TUBG1 complex cortical dysplasia with other brain malformations", "complex cortical dysplasia with other brain malformations type 4", "cortical dysplasia, Complex, with Other brain malformations type 4", "complex cortical dysplasia with other brain malformations caused by mutation in TUBG1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complex cortical dysplasia with other brain malformations 4", "shortest_name_length": 6}
{"curie": "UMLS:C3273102", "names": ["Gallbladder Cystadenocarcinoma", "Gallbladder MCN with an Associated Invasive Carcinoma", "Gallbladder Mucinous Cystic Neoplasm with an Associated Invasive Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gallbladder Mucinous Cystic Neoplasm with an Associated Invasive Carcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0016852", "names": ["UPD(X)pat", "paternal uniparental disomy of chromosome X", "paternal uniparental disomy of chromosome type X"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paternal uniparental disomy of chromosome X", "shortest_name_length": 9}
{"curie": "UMLS:C0684572", "names": ["Metastasis to the Sternum", "Metastatic Tumor to the Sternum", "Metastatic Neoplasm to the Sternum", "Secondary malignant neoplasm of sternum", "Metastatic malignant neoplasm of sternum", "Metastatic malignant neoplasm to sternum", "Metastatic Malignant Tumor to the Sternum", "Metastatic Malignant Neoplasm in the Sternum", "bone neoplasm, malignant - sternum secondary", "Metastatic Malignant Neoplasm to the Sternum", "Secondary malignant neoplasm of sternum (diagnosis)", "Metastatic malignant neoplasm to sternum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to sternum", "shortest_name_length": 25}
{"curie": "MONDO:0015612", "names": ["Dent disease", "Dent Disease", "Disease, Dent", "Dents disease", "Dent syndrome", "Dents Disease", "Dent's Disease", "Dent disease 1", "Dent's disease", "Disease, Dents", "Dent disease 2", "Disease, Dent's", "Dent's disease (disorder)", "X-linked recessive nephrolithiasis", "NEPHROLITHIASIS, X-LINKED RECESSIVE", "X-linked recessive hypophosphatemic rickets", "X-linked Recessive Hypophosphatemic Rickets", "X-Linked Recessive Hypophosphatemic Rickets", "X-linked recessive hypercalciuric hypophosphatemic rickets", "renal Fanconi syndrome with nephrocalcinosis and renal stones", "Renal Fanconi syndrome with nephrocalcinosis and renal stones", "low-molecular-weight proteinuria with hypercalciuria and nephrocalcinosis", "Low-molecular-weight proteinuria with hypercalciuria and nephrocalcinosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dent disease", "shortest_name_length": 12}
{"curie": "MONDO:0019182", "names": ["Leanness", "LEANNESS", "Thinness", "leanness", "thinness", "thin build", "Low weight", "LOW WEIGHT", "weight low", "low weight", "Thin build", "Underweight", "underweight", "UNDERWEIGHT", "Skinny build", "Thinness, NOS", "low body weight", "genetic obesity", "WEIGHT DECREASE", "Low body weight", "Weight decrease", "Decreased;weight", "decreased weight", "Decreased weight", "Weight decreased", "inherited obesity", "monogenic obesity", "Thin body habitus", "weight loss severe", "severe weight loss", "Patient underweight", "WEIGHT LOSS, SEVERE", "patient underweight", "Thin build (finding)", "Underweight (finding)", "Decreased body weight", "underweight (diagnosis)", "weight of patient too low", "genetic obesity (disease)", "Excessive body weight loss", "Body weight loss, excessive", "patient's weight was too low", "thin build (physical finding)", "Weight less than 3rd percentile", "low body weight (physical finding)", "obesity, severe, Autosomal recessive", "obesity, late-onset, Autosomal recessive", "leanness, inherited, autosomal recessive", "obesity, association with, Autosomal recessive", "obesity, mild, early-onset, Autosomal recessive", "obesity, susceptibility to, Autosomal recessive", "obesity, severe, and type II diabetes, Autosomal recessive", "obesity, early-onset, susceptibility to, Autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited obesity", "shortest_name_length": 8}
{"curie": "UMLS:C0014647", "names": ["PGCG", "giant cell epulis", "Giant cell epulis", "Giant Cell Epulis", "Epulis, Giant Cell", "Giant Cell Epulides", "Epulides, Giant Cell", "Giant cell epulis (disorder)", "peripheral giant cell granuloma", "Giant cell peripheral granuloma", "Peripheral Giant Cell Granuloma", "Peripheral giant cell granuloma", "Giant cell granuloma peripheral", "PGCG - Peripheral giant cell granuloma", "periodontal peripheral giant cell granuloma", "periodontal peripheral giant cell granuloma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Giant Cell Epulis", "shortest_name_length": 4}
{"curie": "EFO:1001466", "names": ["Graves ophthalmopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Graves ophthalmopathy", "shortest_name_length": 21}
{"curie": "UMLS:C4521744", "names": ["IIB", "Stage IIB Esophageal Squamous Cell Cancer", "Pathologic Stage IIB Esophageal Squamous Cell Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IIB Esophageal Squamous Cell Carcinoma AJCC v8", "shortest_name_length": 3}
{"curie": "MONDO:0013313", "names": ["EDCS", "EDSS2", "ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 2", "ectodermal dysplasia-syndactyly syndrome 2", "Ectodermal dysplasia-cutaneous syndactyly syndrome", "ectodermal dysplasia-cutaneous syndactyly syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia-cutaneous syndactyly syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0001765", "names": ["Peripheral neuropathy, collagen vascular", "Polyneuropathy in collagen vascular disease", "polyneuropathy in collagen vascular disease", "Polyneuropathy in collagen vascular disease (disorder)", "Neuropathy in vasculitis and connective tissue disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyneuropathy in collagen vascular disease", "shortest_name_length": 40}
{"curie": "MONDO:0005301", "names": ["MS", "ms", "insular sclerosis", "Multiple Sclerosis", "SCLEROSIS, INSULAR", "multiple sclerosis", "sclerosis; insular", "insular; sclerosis", "MULTIPLE SCLEROSIS", "Sclerosis multiple", "SCLEROSIS MULTIPLE", "Multiple sclerosis", "multiples sclerosis", "Sclerosis, Multiple", "sclerosis; multiple", "SCLEROSIS, MULTIPLE", "MS multiple sclerosis", "multiple sclerosis MS", "Multiple sclerosis NOS", "Disseminated Sclerosis", "Disseminated sclerosis", "Sclerosis;disseminated", "disseminated sclerosis", "Multiple sclerosis - MS", "multiple sclerosis (MS)", "MS (Multiple Sclerosis)", "Sclerosis, Disseminated", "sclerosis; disseminated", "MS - Multiple sclerosis", "Multiple sclerosis (MS)", "disseminated; sclerosis", "SCLEROSIS, DISSEMINATED", "Multiple sclerosis, NOS", "sclerosis; cerebrospinal", "cerebrospinal; sclerosis", "DS - Disseminated sclerosis", "obsolete_multiple sclerosis", "Multiple sclerosis (disorder)", "multiple sclerosis (diagnosis)", "Generalized multiple sclerosis", "generalized multiple sclerosis", "generalized multiple sclerosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple sclerosis", "shortest_name_length": 2}
{"curie": "UMLS:C0751750", "names": ["Late-Onset Citrullinemia", "Late-Onset Citrullinemias", "Citrullinemia, Late-Onset", "Citrullinemia, Late Onset", "Deficiency, Argininosuccinic Acid Synthetase, Partial", "Partial Argininosuccinic Acid Synthetase Deficiency Disease", "Argininosuccinic Acid Synthetase Deficiency Disease, Partial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Argininosuccinic Acid Synthetase Deficiency Disease, Partial", "shortest_name_length": 24}
{"curie": "UMLS:C1334978", "names": ["Sporadic Clear Cell Renal Cell Carcinoma", "Non-Hereditary Clear Cell Renal Cell Carcinoma", "Sporadic Conventional (Clear Cell) Renal Cell Carcinoma", "Non-Hereditary Conventional (Clear Cell) Renal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Hereditary Clear Cell Renal Cell Carcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0007226", "names": ["Biemond syndrome", "Biemond's syndrome", "Biemond syndrome type 1", "Biemond syndrome (diagnosis)", "Biemond's syndrome (disorder)", "Brachydactyly-Nystagmus-Cerebellar Ataxia", "brachydactyly-NYSTAGMUS-cerebellar ataxia", "BRACHYDACTYLY-NYSTAGMUS-CEREBELLAR ATAXIA", "brachydactyly - nystagmus - cerebellar ataxia", "brachydactyly, nystagmus and cerebellar ataxia", "brachydactyly-nystagmus-cerebellar ataxia syndrome", "Brachydactyly-nystagmus-cerebellar ataxia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly-nystagmus-cerebellar ataxia syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0019552", "names": ["centrifugal lipodystrophy", "lipodystrophia centrifugalis abdominalis infantilis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "centrifugal lipodystrophy", "shortest_name_length": 25}
{"curie": "MONDO:0014871", "names": ["RP75", "retinitis pigmentosa 75", "RETINITIS PIGMENTOSA 75", "AGBL5 retinitis pigmentosa", "retinitis pigmentosa type 75", "retinitis pigmentosa caused by mutation in AGBL5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 75", "shortest_name_length": 4}
{"curie": "MONDO:0008895", "names": ["ACDC", "CALJA", "Calcification of joints and arteries", "CALCIFICATION OF JOINTS AND ARTERIES", "calcification of joints and arteries", "Calcification of Joints and Arteries", "arterial calcification due to CD73 deficiency", "arterial calcification due to deficiency of Cd73", "arterial calcification due to deficiency of CD73", "ARTERIAL CALCIFICATION DUE TO DEFICIENCY OF CD73", "arterial calcification and distal joint calcification", "hereditary arterial and articular multiple calcification syndrome", "Hereditary arterial and articular multiple calcification syndrome", "Hereditary arterial and articular multiple calcification syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary arterial and articular multiple calcification syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0005276", "names": ["decay", "Caries", "cavity", "caries", "Cavities", "decay tooth", "tooth decay", "saprodontia", "Tooth decay", "Tooth Decay", "Saprodontia", "TOOTH DECAY", "tooth caries", "Tooth caries", "DECAY DENTAL", "decays tooth", "TOOTH CARIES", "Decay dental", "Dental Decay", "Dental decay", "dental decay", "tooth cavity", "DENTAL DECAY", "Decay, Dental", "dental caries", "Caries dental", "Rotting teeth", "Teeth decayed", "carious teeth", "DENTAL CARIES", "Dental cavity", "decayed teeth", "Dental Caries", "CARIES DENTAL", "Carious teeth", "Dental caries", "dental cavity", "Dental Cavity", "Tooth decayed", "Tooth cavities", "Carious lesion", "decaying tooth", "dental; caries", "Carious Lesion", "Caries, Dental", "caries; dental", "Cavity, Dental", "dental cavities", "Dental cavities", "Dental Cavities", "Carious Lesions", "Frequent caries", "Lesion, Carious", "Lesions, Carious", "Tooth caries NOS", "Cavities, Dental", "cavities of teeth", "Cariosity of teeth", "Dental caries, NOS", "Dental cavity, NOS", "caries was observed", "Early dental caries", "Dental caries (disorder)", "dental caries (diagnosis)", "Dental caries, unspecified", "Dental caries pit and fissure", "dental caries pit and fissure", "dental caries of smooth surface", "Dental caries of smooth surface", "Dental caries on smooth surface", "carious teeth (physical finding)", "Dental caries extending into pulp", "dental caries extending into pulp"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dental caries", "shortest_name_length": 5}
{"curie": "MONDO:0017712", "names": ["combined pancreatic lipase-colipase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined pancreatic lipase-colipase deficiency", "shortest_name_length": 46}
{"curie": "MONDO:0012950", "names": ["ANIB10", "intracranial berry aneurysm 10", "aneurysm, intracranial BERRY, 10", "ANEURYSM, INTRACRANIAL BERRY, 10", "Aneurysm, Intracranial Berry, 10", "aneurysm, intracranial berry, 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aneurysm, intracranial berry, 10", "shortest_name_length": 6}
{"curie": "UMLS:C0752252", "names": ["Neuromuscular Manifestation", "neuromuscular manifestation", "Neuromuscular Manifestations", "Manifestation, Neuromuscular", "Manifestations, Neuromuscular", "Neuromuscular Signs and Symptoms", "Signs and Symptoms, Neuromuscular"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neuromuscular Manifestations", "shortest_name_length": 27}
{"curie": "UMLS:C4331297", "names": ["Small Intestinal Myeloid Sarcoma", "Myeloid Sarcoma of the Small Intestine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Intestinal Myeloid Sarcoma", "shortest_name_length": 32}
{"curie": "MONDO:0007888", "names": ["MCL", "LRCC", "MCUL", "HLRCC", "MCUL1", "Reed syndrome", "FH Deficiency", "Reed's syndrome", "leiomyomatosis familial", "familial leiomyomatosis", "Hereditary leiomyomatosis", "hereditary leiomyomatosis", "LEIOMYOMA, MULTIPLE CUTANEOUS", "Multiple cutaneous leiomyomas", "leiomyoma, multiple cutaneous", "Leiomyoma, multiple cutaneous", "multiple cutaneous leiomyomata", "leiomyomatosis and renal cell cancer", "familial leiomyomatosis cutis et uteri", "Familial leiomyomatosis cutis et uteri", "Familial multiple cutaneous leiomyomas", "familial multiple cutaneous leiomyomas", "Leiomyoma, hereditary multiple, of skin", "Hereditary multiple cutaneous leiomyomas", "hereditary multiple cutaneous leiomyomas", "multiple cutaneous and uterine leiomyomas", "Multiple cutaneous and uterine leiomyomas", "multiple cutaneous and uterine leiomyomata", "Multiple cutaneous and uterine leiomyomata 1", "Familial leiomyomatosis with renal carcinoma", "familial leiomyomatosis with renal carcinoma", "Familial leiomyomatosis and renal cell cancer", "Multiple cutaneous and uterine leiomyomatosis", "familial leiomyomatosis and renal cell cancer", "hereditary leiomyomatosis with renal carcinoma", "Hereditary leiomyomatosis with renal carcinoma", "Hereditary leiomyomatosis renal cell carcinoma", "Cutaneous leiomyomata with uterine leiomyomata", "hereditary leiomyomatosis and renal cell cancer", "HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER", "Hereditary leiomyomatosis and renal cell cancer", "Hereditary Leiomyomatosis and Renal Cell Cancer", "leiomyomatosis and renal cell cancer, hereditary", "Leiomyomatosis and renal cell cancer, hereditary", "LEIOMYOMATOSIS AND RENAL CELL CANCER, HEREDITARY", "Hereditary leiomyomatosis and renal cell carcinoma", "hereditary leiomyomatosis and renal cell carcinoma", "Hereditary Leiomyomatosis and Renal Cell Carcinoma", "HLRCC - hereditary leiomyomatosis and renal cell cancer", "hereditary leiomyomatosis and renal cell cancer syndrome", "Hereditary Leiomyomatosis and Renal Cell Carcinoma Syndrome", "Hereditary leiomyomatosis and renal cell carcinoma (disorder)", "Hereditary leiomyomatosis & RCC-associated renal cell carcinoma", "MULTIPLE CUTANEOUS AND UTERINE LEIOMYOMATA 1, WITH OR WITHOUT RENAL CELL CARCINOMA", "multiple cutaneous and uterine leiomyomata 1, with or without renal cell carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary leiomyomatosis and renal cell cancer", "shortest_name_length": 3}
{"curie": "MONDO:0012668", "names": ["Tented eyebrows", "TENTED EYEBROWS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tented eyebrows", "shortest_name_length": 15}
{"curie": "MONDO:0010141", "names": ["TIGLIC ACIDEMIA", "tiglic acidemia", "Tiglic acidemia", "disorder of isoleucine metabolism", "Disorder of isoleucine metabolism", "Disorder of isoleucine metabolism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tiglic acidemia", "shortest_name_length": 15}
{"curie": "MONDO:0023121", "names": ["familial partial paralysis", "partial paralysis, familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial partial paralysis", "shortest_name_length": 26}
{"curie": "MONDO:0012657", "names": ["MGS", "MUNGAN SYNDROME", "Mungan syndrome", "MUNGAN syndrome", "Mungan Syndrome", "pseudoobstruction chronic idiopathic intestinal with Barrett esophagus and cardiac abnormalities", "Pseudoobstruction, Chronic Idiopathic Intestinal, With Barrett Esophagus And Cardiac Abnormalities", "pseudoobstruction, chronic idiopathic intestinal, with Barrett esophagus and Cardiac abnormalities", "PSEUDOOBSTRUCTION, CHRONIC IDIOPATHIC INTESTINAL, WITH BARRETT ESOPHAGUS AND CARDIAC ABNORMALITIES", "visceral neuromyopathy familial with pseudoobstruction megaduodenum Barrett esophagus and cardiac abnormalities", "visceral Neuromyopathy, familial, with pseudoobstruction, Megaduodenum, Barrett esophagus, and Cardiac abnormalities", "VISCERAL NEUROMYOPATHY, FAMILIAL, WITH PSEUDOOBSTRUCTION, MEGADUODENUM, BARRETT ESOPHAGUS, AND CARDIAC ABNORMALITIES", "Visceral Neuromyopathy, Familial, With Pseudoobstruction, Megaduodenum, Barrett Esophagus, And Cardiac Abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mungan syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0016910", "names": ["del(11q)", "deletion 11q", "monosomy 11q", "11q monosomy", "11q deletion", "Deletion 11q partial", "partial monosomy 11q", "monosomy 11q partial", "Monosomy 11q partial", "loss of chromosome 11q", "chromosome 11q deletion", "Chromosome 11q partial deletion", "chromosome 11q partial deletion", "partial monosomy of chromosome 11q", "partial deletion of chromosome 11q", "Partial monosomy of chromosome 11q", "Partial deletion of chromosome 11q", "partial monosomy of the long arm of chromosome 11", "Partial monosomy of the long arm of chromosome 11", "Partial deletion of the long arm of chromosome 11", "partial deletion of the long arm of chromosome 11", "partial deletion of the long arm of chromosome type 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of the long arm of chromosome 11", "shortest_name_length": 8}
{"curie": "UMLS:C2984095", "names": ["Cutaneous Melanoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous Melanoma by AJCC v7 Stage", "shortest_name_length": 35}
{"curie": "UMLS:C1333558", "names": ["FIGO Stage III GTT", "FIGO Stage III Gestational Trophoblastic Tumor", "FIGO Stage III Gestational Trophoblastic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Stage III Gestational Trophoblastic Tumor", "shortest_name_length": 18}
{"curie": "UMLS:C0149893", "names": ["Secondary glaucoma", "Glaucoma secondary", "secondary glaucoma", "SECONDARY GLAUCOMA", "secondary; glaucoma", "Glaucoma, secondary", "glaucoma; secondary", "GLAUCOMA, SECONDARY", "Secondary glaucoma, NOS", "Secondary glaucoma (disorder)", "Glaucoma due to ocular disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary glaucoma", "shortest_name_length": 18}
{"curie": "MONDO:0012135", "names": ["RLS2", "restless legs syndrome 2", "restless legs syndrome, susceptibility to, 2", "RESTLESS LEGS SYNDROME, SUSCEPTIBILITY TO, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "restless legs syndrome, susceptibility to, 2", "shortest_name_length": 4}
{"curie": "UMLS:C0280425", "names": ["Adult T-cell lymphoma/leukemia stage III", "Stage III Adult T-Cell Leukemia/Lymphoma", "stage III adult T-cell leukemia/lymphoma", "Stage III Adult T-Cell Lymphoma/Leukemia", "Adult T-Cell Lymphoma/Leukemia Stage III", "Adult T-cell lymphoma/leukaemia stage III", "adult T-cell leukemia/lymphoma, stage III", "Ann Arbor Stage III Adult T-Cell Leukemia/Lymphoma", "HTLV-1 Associated Adult T-Cell Lymphoma/Leukemia Stage III", "stage III HTLV-I associated adult T-cell leukemia/lymphoma", "Stage III HTLV-1 Associated Adult T-Cell Lymphoma/Leukemia", "HTLV-I associated adult T-cell leukemia/lymphoma, stage III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult T-cell lymphoma/leukemia stage III", "shortest_name_length": 40}
{"curie": "MONDO:0007920", "names": ["LMPH2", "LMPHM5", "Meige Disease", "MEIGE DISEASE", "Meige disease", "LMPH2, FORMERLY", "MEIGE LYMPHEDEMA", "Meige lymphedema", "Meige Lymphedema", "Meige lymphoedema", "Lymphedema Praecox", "lymphedema praecox", "Praecox lymphedema", "LYMPHEDEMA PRAECOX", "primary lymphedema", "Primary lymphedema", "lymphedema preacox", "Lymphedema praecox", "lymphedema primary", "lymphoedema praecox", "praecox; lymphedema", "Lymphedema, praecox", "Lymphoedema praecox", "primary lymphoedema", "late-onset lymphedema", "Adolescent lymphedema", "Adolescent lymphoedema", "LYMPHEDEMA, LATE-ONSET", "Lymphedema, Late-Onset", "lymphedema; precocious", "precocious; lymphedema", "lymphedema, late-onset", "lymphatic malformation 5", "hereditary lymphedema II", "LYMPHATIC MALFORMATION 5", "lymphedema, hereditary, II", "Lymphedema, Hereditary, II", "lymphedema hereditary type 2", "Hereditary lymphedema type II", "late-onset primary lymphedema", "hereditary lymphedema type II", "Lymphedema praecox (disorder)", "Hereditary lymphoedema type II", "LYMPHEDEMA, HEREDITARY, II, FORMERLY", "Hereditary lymphedema type II (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphatic malformation 5", "shortest_name_length": 5}
{"curie": "MONDO:0005594", "names": ["Scar", "SCAR", "scar", "scars", "Scars", "scarred", "Scarred", "scarring", "Scar NOS", "Scarring", "Cicatrix", "cicatrix", "Scar, NOS", "Skin.scar", "skin scar", "Skin scar", "Skin Scar", "cicatrice", "skin; scar", "scars skin", "Cicatrices", "scar; skin", "scar tissue", "Scar tissue", "Scar Tissue", "tissue scar", "Fibrous scar", "healing scar", "scar tissues", "scarred skin", "scars tissue", "Scar of skin", "Healing scar", "fibrous scar", "Cicatrix skin", "skin scarring", "healing scars", "cicatrisation", "SKIN SCARRING", "Skin scarring", "scar disorder", "CICATRIX SKIN", "cicatrization", "scarring skin", "Cicatrization", "Cicatrisation", "scarred tissue", "skin; cicatrix", "Scar (disorder)", "scarring tissue", "Cicatrix of skin", "fibrous scarring", "scar (diagnosis)", "Scar of skin, NOS", "disorders scarring", "Cicatrix of skin, NOS", "scar (physical finding)", "Scar of skin (disorder)", "Scar (morphologic abnormality)", "severe cutaneous adverse reaction", "scar (___cm) (see also by location)", "Healing scar (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe cutaneous adverse reaction", "shortest_name_length": 4}
{"curie": "UMLS:C0039504", "names": ["Tendon injury", "TENDON INJURY", "Tendon Injury", "tendon injury", "Injury, Tendon", "injury tendons", "tendon; injury", "injury; tendon", "Tendon Injuries", "tendon injuries", "injuries tendon", "Injury of tendon", "injuries tendons", "Injuries, Tendon", "tendon injury (diagnosis)", "Injury of tendon (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tendon Injuries", "shortest_name_length": 13}
{"curie": "MONDO:0014947", "names": ["DEE46", "EIEE46", "Early Infantile Epileptic Encephalopathy 46", "early infantile epileptic encephalopathy 46", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 46", "epileptic encephalopathy, early infantile, 46", "Developmental and Epileptic Encephalopathy 46", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 46", "developmental and epileptic encephalopathy 46", "developmental and epileptic encephalopathy, 46", "GRIN2D early infantile epileptic encephalopathy", "epileptic encephalopathy, early infantile, type 46", "epileptic encephalopathy, early infantile, 46; EIEE46", "early infantile epileptic encephalopathy caused by mutation in GRIN2D"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 46", "shortest_name_length": 5}
{"curie": "UMLS:C0156185", "names": ["bowel; abscess", "abscess; bowel", "abscess intestine", "Abscess intestinal", "abscess; intestine", "abscess intestines", "intestinal abscess", "intestinal; abscess", "Abscess of intestine", "abscesses intestinal", "Abscess of intestine, NOS", "intestinal abscess (diagnosis)", "Abscess of intestine (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abscess of intestine", "shortest_name_length": 14}
{"curie": "MONDO:0013860", "names": ["MGN", "MBNP", "membranous GN", "glomerulonephritis, membranous", "Primary membranous nephropathy", "Idiopathic membranous nephropathy", "Idiopathic Membranous Nephropathy", "idiopathic membranous nephropathy", "Membranous Nephropathy, Idiopathic", "Nephropathy, Idiopathic Membranous", "Extramembranous glomerulonephritis", "membranous nephropathy - Idiopathic", "Membranous Nephropathy - Idiopathic", "Idiopathic Membranous Glomerulopathy", "Idiopathic membranous glomerulopathy", "Primary membranous glomerulonephritis", "idiopathic membranous glomerulonephritis", "Idiopathic membranous glomerulonephritis", "Idiopathic Membranous Glomerulonephritis", "membranous glomerulonephritis idiopathic", "Glomerulonephritis, Idiopathic Membranous", "membranous nephropathy, susceptibility to", "Membranous Glomerulonephritis, Idiopathic", "MEMBRANOUS NEPHROPATHY, SUSCEPTIBILITY TO", "Idiopathic Membranous Glomerulonephritides", "Glomerulonephritides, Idiopathic Membranous", "Membranous Glomerulonephritides, Idiopathic", "Idiopathic membranous glomerulonephritis (disorder)", "Idiopathic membranous glomerulonephritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic membranous glomerulonephritis", "shortest_name_length": 3}
{"curie": "UMLS:C5239056", "names": ["Cervical Spine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Spine Neoplasm", "shortest_name_length": 23}
{"curie": "UMLS:C0857122", "names": ["Hyponatremic", "hyponatremic", "Hyponatraemic", "hyponatraemic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyponatraemic", "shortest_name_length": 12}
{"curie": "MONDO:0014419", "names": ["PTBHS", "Poretti Boltshauser syndrome", "PORETTI-Boltshauser syndrome", "PORETTI-BOLTSHAUSER SYNDROME", "Poretti-Boltshauser syndrome", "Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome", "ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome", "Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome", "Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome (disorder)", "Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C4525130", "names": ["Stage IVB Colon Cancer", "Stage IVB Colon Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Colon Cancer AJCC v8", "shortest_name_length": 22}
{"curie": "MONDO:0100498", "names": ["UROD-related inherited porphyria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "UROD-related inherited porphyria", "shortest_name_length": 32}
{"curie": "UMLS:C4330555", "names": ["Lip and Oral Cavity Cancer by AJCC v6 and v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lip and Oral Cavity Cancer by AJCC v6 and v7 Stage", "shortest_name_length": 50}
{"curie": "MONDO:0011208", "names": ["Degos", "Degos Disease", "Degos disease", "DEGOS DISEASE", "degos disease", "degos' disease", "Degos Syndrome", "Disease, Degos", "Degos syndrome", "Degos' disease", "Syndrome, Degos", "Maladie de Degos", "Kohlmeier-Degos Disease", "Kohlmeier-Degos disease", "Köhlmeier-Degos disease", "kohlmeier-degos disease", "Disease, Kohlmeier-Degos", "Kohlmeier-Degos syndrome", "KOEHLMEIER-DEGOS SYNDROME", "CUTANEOINTESTINAL SYNDROME", "papulosis atrophican maligna", "malignant atrophic papulosis", "Malignant Atrophic Papuloses", "MALIGNANT ATROPHIC PAPULOSIS", "Papulosis atrophican maligna", "Malignant Atrophic Papulosis", "Malignant atrophic papulosis", "atrophic papulosis, malignant", "Atrophic Papuloses, Malignant", "PAPULOSIS, MALIGNANT ATROPHIC", "Atrophic Papulosis, Malignant", "Papulosis, Malignant Atrophic", "Papuloses, Malignant Atrophic", "papulosis, malignant atrophic", "PAPULOSIS, MALIGNANT, ATROPHIC", "Erythrokeratoderma en cocardes", "Degos genodermatosis \"en cocardes\"", "MAP - malignant atrophic papulosis", "Erythrokeratoderma ''en cocardes''", "Degos's malignant atrophic papulosis", "Degos's Malignant Atrophic Papulosis", "Erythrokeratoderma en cocarde (Degos)", "Malignant atrophic papulosis of Degos", "Kohlmeier-Degos-Delort-Tricort syndrome", "Malignant atrophic papulosis (disorder)", "Köhlmeier-Degos-Delort-Tricort syndrome", "malignant atrophic papulosis (diagnosis)", "Erythrokeratoderma en cocardes (disorder)", "malignant atrophic papulosis (Degos disease)", "Erythrokeratoderma en cocardes (Degos syndrome)", "Lethal cutaneous and gastrointestinal arteriolar thrombosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant atrophic papulosis", "shortest_name_length": 5}
{"curie": "MONDO:0016416", "names": ["diphallia", "diphallus", "Diphallus", "Diphallia", "Bifid penis", "penis; duplication", "duplication; penis", "Penile duplication", "Diphallus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diphallia", "shortest_name_length": 9}
{"curie": "MONDO:0016872", "names": ["partial deletion of chromosome 7", "partial monosomy of chromosome 7", "partial deletion of chromosome type 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of chromosome 7", "shortest_name_length": 32}
{"curie": "MONDO:0014201", "names": ["EIEE1", "DEE18", "EIEE18", "early infantile epileptic encephalopathy 18", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 18", "epileptic encephalopathy, early infantile, 18", "developmental and epileptic encephalopathy 18", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 18", "developmental and epileptic encephalopathy, 18", "epileptic encephalopathy, early infantile, type 18", "early infantile epileptic encephalopathy without suppression burst"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 18", "shortest_name_length": 5}
{"curie": "MONDO:0014304", "names": ["SPG61", "hereditary spastic paraplegia 61", "hereditary spastic paraplegia type 61", "autosomal recessive spastic paraplegia 61", "SPASTIC PARAPLEGIA 61, AUTOSOMAL RECESSIVE", "spastic paraplegia 61, autosomal recessive", "Autosomal recessive spastic paraplegia type 61", "autosomal recessive spastic paraplegia type 61", "ARL6IP1 autosomal recessive complex spastic paraplegia", "familial spastic paraplegia autosomal recessive type 61", "Autosomal recessive spastic paraplegia type 61 (disorder)", "Autosomal recessive spastic paraplegia type 61 (diagnosis)", "autosomal recessive complex spastic paraplegia caused by mutation in ARL6IP1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 61", "shortest_name_length": 5}
{"curie": "UMLS:C0863113", "names": ["Hypotension symptomatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypotension symptomatic", "shortest_name_length": 23}
{"curie": "MONDO:0006498", "names": ["Colon Adenomatous Polyp", "colon adenomatous polyp", "adenomatous colon polyp", "Colonic Adenomatous Polyp", "colonic adenomatous polyp", "Adenomatous Polyp of Colon", "adenomatous polyp of colon", "adenomatous polyp of the colon", "Adenomatous Polyp of the Colon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenomatous colon polyp", "shortest_name_length": 23}
{"curie": "MONDO:0009348", "names": ["cHL", "CHL", "Chl", "Hodgkin disease", "Classic Hodgkin disease", "classic Hodgkin disease", "Classic Hodgkin lymphoma", "Classic Hodgkin Lymphoma", "classic Hodgkin lymphoma", "lymphoma, Hodgkin, classic", "classical Hodgkin lymphoma", "Classical Hodgkin lymphoma", "Classical Hodgkin Lymphoma", "Classical Hodgkin's Lymphoma", "classical Hodgkin's lymphoma", "Classical Hodgkin lymphoma NOS", "Hodgkin lymphoma, susceptibility to", "Classical Hodgkin lymphoma (disorder)", "Classical Hodgkin lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "classic Hodgkin lymphoma", "shortest_name_length": 3}
{"curie": "UMLS:C0221082", "names": ["Surgical complication", "Surgical Complication", "surgical complication", "Surgical Complications", "surgical complications", "complications surgical", "Adverse effect;surgery", "adverse effects surgery", "adverse effect due to surgery", "Etiology, operative procedure, as cause of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Surgical Complication", "shortest_name_length": 21}
{"curie": "UMLS:C1332179", "names": ["Adult Acute Lymphoid Leukemia in Complete Remission", "Adult Acute Lymphocytic Leukemia in Complete Remission", "Adult Acute Lymphogenous Leukemia in Complete Remission", "Adult Acute Lymphoblastic Leukemia in Complete Remission", "Acute Lymphoblastic Leukemia (ALL) in Complete Remission", "Adult Precursor Lymphoblastic Leukemia in Complete Remission"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Acute Lymphoblastic Leukemia in Complete Remission", "shortest_name_length": 51}
{"curie": "MONDO:0100374", "names": ["M4eo", "M4eos", "FAB M4E", "AMML Eo", "FAB M4Eo", "AML, t(16;16)(p13q22)", "AML, t(16;16)(p13;q22)", "AML, t(16;16)(p13.1q22)", "AML, t(16;16)(p13.1;q22)", "AML, t(16;16)(p13.1q22.1)", "AML, t(16;16)(p13.1;q22.1)", "Acute myeloid leukemia, CBF-beta/MYH11", "Acute Myeloid Leukemia, inv(16)(p13q22)", "Acute myeloid leukemia, inv(16)(p13q22)", "Acute myeloid leukaemia, CBF-beta/MYH11", "Acute myeloid leukaemia, inv(16)(p13q22)", "Acute myeloid leukemia, t(16;16)(p13;q22)", "Acute Myeloid Leukemia, t(16;16)(p13;q22)", "Acute myeloid leukaemia, t(16;16)(p13;q22)", "acute myeloid leukemia, t(16;16)(p13.1;q22)", "Acute Myeloid Leukemia with inv(16)(p13q22)", "Acute myeloid leukemia, t(16;16)(p 13;q 11)", "Acute Myeloid Leukemia with t(16;16)(p13;q22)", "Acute myelomonocytic leukemia with eosinophils", "Acute myelomonocytic leukaemia with eosinophils", "acute myeloid leukemia with abnormal marrow eosinophils", "Acute myeloid leukemia with abnormal marrow eosinophils", "Acute Myelomonocytic Leukemia with Abnormal Eosinophils", "Acute Myeloid Leukemia with inv(16)(p13q22)(CBFb/MYH11)", "Acute myelomonocytic leukemia with abnormal eosinophils", "Acute myelomonocytic leukaemia with abnormal eosinophils", "Acute myeloid leukaemia with abnormal marrow eosinophils", "Acute Myeloid Leukemia with inv(16)(p13.1q22); CBFB-MYH11", "Acute Myeloid Leukemia with t(16;16)(p13.1;q22); CBFB-MYH11", "acute myeloid leukemia with inv(16)(p13.1q22) or t(16;16)(p13.1;q22)", "Acute Myeloid Leukemia with inv(16)(p13.1q22) or t(16;16)(p13.1;q22); CBFB-MYH11", "Acute myeloid leukemia with abnormal marrow eosinophils and inv(16)(p13q22) or t(16;16)(p13;q22)", "Acute myeloid leukaemia with abnormal marrow eosinophils and inv(16)(p13q22) or t(16;16)(p13;q22)", "Acute myeloid leukemia with abnormal marrow eosinophils and inv(16)(p13q22) or t(16;16)(p13;q22) (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, t(16;16)(p13.1;q22)", "shortest_name_length": 4}
{"curie": "UMLS:C0745528", "names": ["KLEBSIELLA SEPSIS", "Klebsiella sepsis", "Klebsiella septicemia", "Klebsiella septicaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Klebsiella sepsis", "shortest_name_length": 17}
{"curie": "UMLS:C0018128", "names": ["Vascular graft occlusion", "Vascular Graft Occlusion", "Occlusion, Vascular Graft", "Vascular graft restenosis", "Vascular Graft Restenosis", "Graft Occlusion, Vascular", "Graft Restenosis, Vascular", "Graft Restenoses, Vascular", "Restenosis, Vascular Graft", "Vascular graft occlusion (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Graft Occlusion, Vascular", "shortest_name_length": 24}
{"curie": "MONDO:0001720", "names": ["Gonococcal synovitis", "gonococcal synovitis", "Gonococcal synovitis (disorder)", "gonococcal synovitis (diagnosis)", "Gonococcal synovitis or tenosynovitis", "gonococcal synovitis or tenosynovitis", "gonococcal synovitis and tenosynovitis", "Gonococcal synovitis and tenosynovitis", "Gonococcal synovitis &/or tenosynovitis", "gonococcal synovitis &/or tenosynovitis", "gonococcal infections synovitis or tenosynovitis", "Gonococcal synovitis or tenosynovitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gonococcal synovitis", "shortest_name_length": 20}
{"curie": "MONDO:0007475", "names": ["duodenal ulcer, hyperpepsinogenemic I", "DUODENAL ULCER, HYPERPEPSINOGENEMIC I", "duodenal ulcer, hyperpepsinogenemic 1", "Duodenal Ulcer, Hyperpepsinogenemic I", "duodenal Ulcer, hyperpepsinogenemic type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "duodenal ulcer, hyperpepsinogenemic 1", "shortest_name_length": 37}
{"curie": "MONDO:0100431", "names": ["Migraine;common", "common migraine", "Common Migraine", "Common migraine", "common; migraine", "migraine; common", "common migraines", "Migraine, Common", "Common Migraines", "migraine atypical", "atypical migraine", "Atypical migraine", "Migraines, Common", "atypical migraines", "migraine without aura", "Migraine without Aura", "Migraine Without Aura", "Migraine without aura", "migraine; without aura", "Migraine without aura NOS", "common migraine without aura", "Migraine without aura (disorder)", "Migraine without aura [common migraine]", "common migraine without aura (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "migraine without aura", "shortest_name_length": 15}
{"curie": "MONDO:0015481", "names": ["Cleft lower eyelid", "Lower lid coloboma", "Notched lower eyelid", "Coloboma of lower lid", "Lower eyelid coloboma", "Coloboma, lower eyelid", "Coloboma of lower eyelid", "coloboma of inferior eyelid", "Inferior palpebral coloboma", "Coloboma of inferior eyelid", "Coloboma of the lower eyelids", "congenital eyelid coloboma inferior", "Coloboma of inferior eyelid (disorder)", "Coloboma of inferior eyelid (diagnosis)", "Full thickness defect of the lower eyelid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coloboma of inferior eyelid", "shortest_name_length": 18}
{"curie": "MONDO:0003884", "names": ["rectal lipoma", "rectum lipoma", "Rectal Lipoma", "Lipoma of Rectum", "lipoma of rectum", "lipoma of the rectum", "Lipoma of the Rectum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lipoma of the rectum", "shortest_name_length": 13}
{"curie": "UMLS:C1275959", "names": ["Cellular Neurothekeoma", "Cellular neurothekeoma", "Cellular Nerve Sheath Myxoma", "Cellular nerve sheath myxoma", "Cellular neurothekeoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cellular neurothekeoma", "shortest_name_length": 22}
{"curie": "MONDO:0003803", "names": ["AOVD", "AORTIC VALVE DEFECT", "aortic valve defect", "Aortic valve disease", "aortic valve disease", "Aortic valve defects", "aortic defects valve", "Aortic Valve Disease", "AORTIC VALVE DISEASE", "Aortic Heart Disease", "aortic valve diseases", "Heart Disease, Aortic", "aortic valve disorder", "Aortic Valve Disorder", "Aortic Heart Diseases", "Aortic valve disorder", "Aortic Valve Diseases", "Valve Disease, Aortic", "Aortic valve disorders", "Valve Disorder, Aortic", "Aortic Valve Disorders", "aortic valve disorders", "aortic valve; disorder", "disease of aortic valve", "aortic valvular disease", "Diseases of aortic valve", "disorder of aortic valve", "Aortic valve disease NOS", "Aortic valvular disorders", "AVD - Aortic valve disease", "Aortic valve disorder, NOS", "Aortic Valvular Heart Disease", "heart; disease, aorta (valve)", "Aortic Valvular Heart Disorder", "aortic valve disease or disorder", "Aortic valve disorder (disorder)", "aortic valve disorder (diagnosis)", "Aortic valve disorder, unspecified", "disease or disorder of aortic valve", "disease (or disorder); heart, aorta (valve)", "disease (or disorder); aortic valve (heart)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic valve disorder", "shortest_name_length": 4}
{"curie": "MONDO:0015360", "names": ["autosomal dominant hereditary axonal motor and sensory neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant hereditary axonal motor and sensory neuropathy", "shortest_name_length": 65}
{"curie": "MONDO:0009729", "names": ["Edwards Patton Dilly syndrome", "Edwards-Patton-Dilly syndrome", "Nephropathy deafness hyperparathyroidism", "nephropathy - deafness - hyperparathyroidism", "NEPHROPATHY, DEAFNESS, AND HYPERPARATHYROIDISM", "Nephropathy, Deafness, And Hyperparathyroidism", "nephropathy, deafness, and hyperparathyroidism", "Nephropathy-deafness-hyperparathyroidism syndrome", "Nephropathy, deafness, hyperparathyroidism syndrome", "Nephropathy-hearing loss-hyperparathyroidism syndrome", "nephropathy - deafness - hyperparathyroidism syndrome", "Nephropathy, deafness, hyperparathyroidism syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephropathy - deafness - hyperparathyroidism syndrome", "shortest_name_length": 29}
{"curie": "UMLS:C0343361", "names": ["Adenovirus food poisoning", "gastroenteritis adenovirus", "Gastroenteritis adenovirus", "adenovirus gastroenteritis", "Adenovirus food poisoning (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenovirus food poisoning", "shortest_name_length": 25}
{"curie": "UMLS:C3273258", "names": ["Congenital Systemic Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Systemic Disorder", "shortest_name_length": 28}
{"curie": "MONDO:0041114", "names": ["ischemia peripheral", "Peripheral ischemia", "PERIPHERAL ISCHEMIA", "Peripheral Ischemia", "peripheral ischemia", "ISCHEMIA PERIPHERAL", "Ischemia peripheral", "Ischaemia peripheral", "Peripheral ischaemia", "peripheral ischaemia", "ISCHAEMIA PERIPHERAL", "PERIPHERAL ISCHAEMIA", "Peripheral ischemia NOS", "Peripheral ischaemia NOS", "Peripheral ischemia (disorder)", "peripheral ischemia (diagnosis)", "peripheral ischemic vascular disease", "Peripheral ischemic vascular disease", "Peripheral ischaemic vascular disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peripheral ischemia", "shortest_name_length": 19}
{"curie": "MONDO:0035444", "names": ["Acute MCL", "acute mast cell leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute mast cell leukemia", "shortest_name_length": 9}
{"curie": "MONDO:0020504", "names": ["genetic recurrent myoglobinuria", "Genetic recurrent myoglobinuria", "Genetic recurrent myoglobinuria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genetic recurrent myoglobinuria", "shortest_name_length": 31}
{"curie": "MONDO:0001048", "names": ["orbit; granuloma", "granuloma; orbit", "Orbital Granuloma", "Orbital granuloma", "orbital granuloma", "granulomas orbital", "Granuloma of orbit", "Orbital granuloma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orbital granuloma", "shortest_name_length": 16}
{"curie": "MONDO:0013032", "names": ["EIG8", "CASR generalised epilepsy", "idiopathic generalized epilepsy 8", "generalised epilepsy caused by mutation in CASR", "susceptibility to idiopathic generalized epilepsy 8", "epilepsy idiopathic generalized, susceptibility to, 8", "EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 8", "epilepsy, idiopathic generalized, susceptibility to, 8", "epilepsy, idiopathic generalized, susceptibility to, type 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, idiopathic generalized, susceptibility to, 8", "shortest_name_length": 4}
{"curie": "MONDO:0009929", "names": ["SMDP1", "Surfactant Protein B Deficiency", "Surfactant Apoprotein B Deficiency", "Pulmonary Alveolar Proteinosis, Congenital, 1", "pulmonary surfactant protein B, deficiency of", "pulmonary alveolar proteinosis, congenital, 1", "Pulmonary Surfactant Metabolism Dysfunction-1", "PULMONARY ALVEOLAR PROTEINOSIS, CONGENITAL, 1", "SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 1", "Surfactant Metabolism Dysfunction, Pulmonary, 1", "surfactant metabolism dysfunction, pulmonary, 1", "surfactant metabolism dysfunction, pulmonary, type 1", "neonatal acute respiratory distress due to SP-B deficiency", "Neonatal acute respiratory distress due to SP-B deficiency", "interstitial lung disease due to surfactant Protein B deficiency", "Interstitial Lung Disease Due To Surfactant Protein B Deficiency", "INTERSTITIAL LUNG DISEASE DUE TO SURFACTANT PROTEIN B DEFICIENCY", "Neonatal acute respiratory distress due to surfactant protein B deficiency", "neonatal acute respiratory distress due to surfactant protein B deficiency", "Interstitial Lung Disease, Nonspecific, Due To Surfactant Protein B Deficiency", "INTERSTITIAL LUNG DISEASE, NONSPECIFIC, DUE TO SURFACTANT PROTEIN B DEFICIENCY", "interstitial lung disease, nonspecific, due to surfactant Protein B deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal acute respiratory distress due to SP-B deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C1332173", "names": ["Adherence syndrome", "Adherence Syndrome", "Fat adherence syndrome of extraocular muscle", "Fat adherence syndrome of extraocular muscle (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fat adherence syndrome of extraocular muscle", "shortest_name_length": 18}
{"curie": "UMLS:C4727363", "names": ["Recurrent Anal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Anal Adenocarcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0010011", "names": ["Porencephaly", "porencephaly", "PORENCEPHALY", "Porencephalia", "Porencephalus", "schizencephaly", "Schizencephaly", "SCHIZENCEPHALY", "Schizencephalies", "Schizencephalic Cyst", "Schizencephalic Cleft", "Cyst, Schizencephalic", "Schizencephalic Cysts", "Schizencephalic Clefts", "Cleft, Schizencephalic", "Schizencephalic clefts", "Cysts, Schizencephalic", "Congenital porencephaly", "Congenital Porencephaly", "Clefts, Schizencephalic", "Congenital porencephalia", "Porencephaly, Congenital", "porencephaly (diagnosis)", "Porencephaly, congenital", "Schizencephaly (disorder)", "schizencephaly (diagnosis)", "Congenital cerebral porosis", "Schizencephalic porencephaly", "Congenital porencephaly (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schizencephaly", "shortest_name_length": 12}
{"curie": "UMLS:C4682641", "names": ["Stage IVB Primary Peritoneal Cancer", "Stage IVB Primary Peritoneal Cancer AJCC v8", "Stage IVB Primary Peritoneal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Primary Peritoneal Cancer AJCC v8", "shortest_name_length": 35}
{"curie": "MONDO:0042983", "names": ["phakomatosis", "phakomatoses", "phacomatosis", "Phakomatoses", "Phacomatosis", "phacomatoses", "Phacomatoses", "Phakomatosis", "Phakomatosis, NOS", "neurocutaneous disorder", "Neurocutaneous syndrome", "neurocutaneous syndrome", "Neurocutaneous Syndrome", "Neurocutaneous Disorder", "neurocutaneous syndromes", "neurocutaneous disorders", "Phakomatoses (diagnosis)", "Neurocutaneous Disorders", "Neurocutaneous Syndromes", "Syndrome, Neurocutaneous", "Neurocutaneous disorders", "syndrome, neurocutaneous", "Syndromes, Neurocutaneous", "syndromes, neurocutaneous", "Phakomatosis, unspecified", "neuroectodermal dysplasia", "Neuroectodermal dysplasia", "anomalies of skin phakomatoses", "Neuroectodermal dysplasia, NOS", "Neuroectodermal Dysplasia Syndrome", "Neurocutaneous syndrome (disorder)", "neuroectodermal dysplasia syndrome", "Neuroectodermal Dysplasia Syndromes", "neuroectodermal dysplasia syndromes", "syndrome, neuroectodermal dysplasia", "Syndrome, Neuroectodermal Dysplasia", "neurocutaneous disorders (diagnosis)", "Syndromes, Neuroectodermal Dysplasia", "syndromes, neuroectodermal dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurocutaneous syndrome", "shortest_name_length": 12}
{"curie": "UMLS:C1335044", "names": ["Non-Neoplastic Sternal Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Sternal Disorder", "shortest_name_length": 31}
{"curie": "UMLS:C5669685", "names": ["Advanced Fibrolamellar Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Fibrolamellar Carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0005578", "names": ["Arthritis", "arthritis", "ARTHRITIS", "arthritide", "arthritides", "Arthritides", "Arthritis NOS", "inflamed joint", "Joint inflamed", "Inflamed joint", "Arthritis, NOS", "inflamed joints", "Joint inflammation", "JOINT INFLAMMATION", "joint inflammation", "joint; inflammation", "inflammation joints", "inflammation; joint", "joints inflammation", "Arthritis (disorder)", "arthritis (diagnosis)", "Inflammation;joint(s)", "Arthritis;inflammatory", "Inflammatory arthritis", "ARTHRITIS INFLAMMATORY", "Arthritis, unspecified", "inflammatory arthritis", "arthritic joint disease", "Arthritis, inflammatory", "Inflamed joint (finding)", "Inflammatory arthropathy", "Inflammation of joint NOS", "INFLAMMATORY ARTHROPATHIES", "skeletal joint inflammation", "inflammation of the joint(s)", "inflammatory disorder of joint", "Inflammatory disorder of joint", "inflammation of skeletal joint", "Arthritis, unspecified, site unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthritic joint disease", "shortest_name_length": 9}
{"curie": "MONDO:0009781", "names": ["ONYCHOTRICHODYSPLASIA AND NEUTROPENIA", "Onychotrichodysplasia and neutropenia", "onycho-tricho-dysplasia-neutropenia syndrome", "Onychotrichodysplasia, chronic neutropenia and mental retardation syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Onychotrichodysplasia and neutropenia", "shortest_name_length": 37}
{"curie": "MONDO:0018468", "names": ["PPIRee", "PPI-REE", "PPI-responsive esophageal eosinophilia", "proton-pump inhibitor-responsive esophageal eosinophilia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "proton-pump inhibitor-responsive esophageal eosinophilia", "shortest_name_length": 6}
{"curie": "UMLS:C4721652", "names": ["Stage III Fallopian Tube Cancer", "stage III fallopian tube cancer", "stage III fallopian tube cancer AJCC v7", "Stage III Fallopian Tube Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Fallopian Tube Cancer AJCC v7", "shortest_name_length": 31}
{"curie": "MONDO:0011570", "names": ["CMT2B2", "Arcmt2B", "ARCMT2B", "CMT 2B2", "AR-CMT2B2", "autosomal recessive axonal CMT4C3", "Autosomal recessive axonal CMT4C3", "Charcot Marie Tooth disease type 2B2", "Charcot-Marie-Tooth disease type 2B2", "Charcot-Marie-Tooth disease, type 2B2", "Charcot-Marie-Tooth disease, Type 2B2", "Charcot-Marie-Tooth neuropathy type 2B2", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2B2", "MED25 Charcot-Marie-Tooth disease type 2", "Charcot-Marie-Tooth Neuropathy, Type 2B2", "Charcot-Marie-Tooth neuropathy, type 2B2", "Charcot-Marie-Tooth disease, axonal, type 2B2", "Charcot-Marie-Tooth disease neuronal type 2B2", "Charcot-Marie-Tooth disease, axonal, Type 2B2", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B2", "Charcot-Marie-Tooth disease, neuronal, type 2B2", "Charcot-Marie-Tooth disease, neuronal, Type 2B2", "CHARCOT-MARIE-TOOTH DISEASE, NEURONAL, TYPE 2B2", "Charcot-Marie-Tooth disease type 2B2 (disorder)", "Charcot-Marie-Tooth disease type 2B2 (diagnosis)", "Charcot-Marie-Tooth disease, axonal, autosomal recessive, B2", "Charcot-Marie-Tooth disease type 2 caused by mutation in MED25", "autosomal recessive axonal Charcot-Marie-Tooth disease type 2B2", "Autosomal recessive axonal Charcot-Marie-Tooth disease type 2B2", "Charcot-Marie-Tooth Disease, Axonal, Autosomal Recessive, Type B2", "Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2B2", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2B2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 2B2", "shortest_name_length": 6}
{"curie": "UMLS:C4551542", "names": ["Stage IVA Vaginal Cancer", "Vaginal Cancer Stage IVA", "AJCC Stage IVA Vaginal Cancer", "FIGO Stage IVA Vagina Carcinoma", "FIGO Stage IVA Vaginal Carcinoma", "Stage IVA Vaginal Cancer AJCC v7", "Stage IVA Vaginal Cancer AJCC v6", "FIGO Stage IVA Carcinoma of Vagina", "Stage IVA Vaginal Carcinoma AJCC v6", "Stage IVA Vaginal Carcinoma AJCC v7", "FIGO Stage IVA Carcinoma of the Vagina", "Stage IVA Vaginal Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Vaginal Cancer AJCC v6 and v7", "shortest_name_length": 24}
{"curie": "UMLS:C5206441", "names": ["Stage IB2 Cervical Cancer FIGO 2018", "Stage IB2 Cervical Carcinoma FIGO 2018"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB2 Cervical Cancer FIGO 2018", "shortest_name_length": 35}
{"curie": "MONDO:0009875", "names": ["ACHM3", "Achm3", "ACHM1", "RMCH1", "ACHM 3", "Pingelapese", "ACHROMATOPSIA 3", "Achromatopsia 3", "RMCH1, FORMERLY", "achromatopsia 3", "ACHM1, FORMERLY", "ACHM1, formerly", "RMCH1 (formerly)", "ACHM1 (formerly)", "rod monochromacy 1", "CNGB3 achromatopsia", "rod monochromatism 1", "achromatopsia type 3", "Pingelapese Blindness", "Pingelapese blindness", "PINGELAPESE BLINDNESS", "Achromatopsia with myopia", "achromatopsia with myopia", "ACHROMATOPSIA WITH MYOPIA", "rod monochromacy 1, formerly", "ROD MONOCHROMACY 1, FORMERLY", "Rod monochromacy 1 (formerly)", "ROD MONOCHROMATISM 1, FORMERLY", "rod monochromatism 1, formerly", "Rod monochromatism 1 (formerly)", "Total colorblindness with myopia", "total colorblindness with myopia", "TOTAL COLORBLINDNESS WITH MYOPIA", "achromatopsia caused by mutation in CNGB3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "achromatopsia 3", "shortest_name_length": 5}
{"curie": "MONDO:0019941", "names": ["HSAN2", "HSANII", "HMSN II", "HSN Type II", "HSN Type IIs", "HMSN Type II", "HSAN Type II", "Painless whitlow disease", "Neurogenic acroosteolysis", "neurogenic acroosteolysis", "Giaccai type acroosteolysis", "Giaccai Type Acroosteolysis", "Acroosteolysis, Giaccai Type", "Charcot-Marie-Tooth disease Type 2", "Charcot Marie Tooth disease, type 2", "Charcot-Marie-Tooth disease, type II", "Charcot-Marie-Tooth Disease, Type II", "Charcot Marie Tooth Disease, Type II", "hereditary sensory neuropathy type 2", "Autosomal recessive sensory neuropathy", "Peroneal muscular atrophy of neuronal type", "Hereditary sensory-motor neuropathy, type 2", "Inherited neuronal peroneal muscular atrophy", "Neuropathy, Progressive Sensory, Of Children", "Hereditary sensory-motor neuropathy, type II", "Charcot-Marie-Tooth disease of neuronal type", "Peroneal muscular atrophy, inherited, neuronal", "Charcot-Marie-Tooth disease Type 2 (diagnosis)", "Hereditary motor and sensory neuropathy type 2", "Dominant hereditary sensory neuropathy, type II", "Hereditary motor and sensory neuropathy type II", "Hereditary Motor and Sensory-Neuropathy Type II", "Hereditary sensory neuropathy, type 2, dominant", "Charcot-Marie-Tooth disease, type II (disorder)", "Hereditary Motor and Sensory Neuropathy Type II", "Hereditary Sensory Autonomic Neuropathy, Type 2", "Neuropathy, Type II Hereditary Motor and Sensory", "autosomal recessive sensory radicular neuropathy", "Autosomal recessive sensory radicular neuropathy", "Hereditary sensory and autonomic neuropathy type 2", "hereditary sensory and autonomic neuropathy type 2", "Hereditary Sensory and Autonomic Neuropathy Type 2", "hereditary sensory and autonomic neuropathy type II", "Hereditary Sensory and Autonomic Neuropathy Type II", "Hereditary sensory and autonomic neuropathy type II", "Hereditary sensory and autonomic neuropathy, type II", "Hereditary Sensory Radicular Neuropathy, Recessive Form", "hereditary sensory radicular neuropathy, recessive form", "Neuropathy, Hereditary Sensory Radicular, Autosomal Recessive", "Hereditary sensory and autonomic neuropathy type II (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary sensory and autonomic neuropathy type 2", "shortest_name_length": 5}
{"curie": "MONDO:0020778", "names": ["Crdhl", "CRDHL", "CRDHL1", "cone-rod dystrophy and hearing loss", "CONE-ROD DYSTROPHY AND HEARING LOSS 1", "cone-rod dystrophy and hearing loss 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cone-rod dystrophy and hearing loss 1", "shortest_name_length": 5}
{"curie": "UMLS:C1514511", "names": ["Prostate Ductal Adenocarcinoma, Cribriform Pattern"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Ductal Adenocarcinoma, Cribriform Pattern", "shortest_name_length": 50}
{"curie": "UMLS:C2981626", "names": ["Stage III Intrahepatic Cholangiocarcinoma", "Stage III Intrahepatic Cholangiocarcinoma AJCC v7", "Stage III Intrahepatic Bile Duct Cancer (Cholangiocarcinoma)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Intrahepatic Cholangiocarcinoma AJCC v7", "shortest_name_length": 41}
{"curie": "MONDO:0006290", "names": ["germ cell cancer", "cancer of germ cell", "Germ cell cancer, NOS", "malignant germ cell tumor", "Malignant Germ Cell Tumor", "germ cell tumor, malignant", "Malignant Tumor of Germ Cell", "malignant tumor of germ cell", "malignant germ cell neoplasm", "Malignant germ cell neoplasm", "Malignant Germ Cell Neoplasm", "malignant neoplasm of germ cell", "Malignant Neoplasm of Germ Cell", "Malignant Tumor of the Germ Cell", "malignant tumor of the germ cell", "Primary malignant germ cell tumor", "Primary malignant germ cell tumour", "malignant neoplasm of the germ cell", "Malignant Neoplasm of the Germ Cell", "Primary malignant germ cell neoplasm", "Primary malignant germ cell neoplasm (disorder)", "Malignant germ cell neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant germ cell tumor", "shortest_name_length": 16}
{"curie": "MONDO:0007642", "names": ["Absent gallbladder", "gallbladder agenesis", "Gallbladder agenesis", "atresia; gallbladder", "agenesis gallbladder", "gallbladder; atresia", "gallbladder; agenesis", "agenesis; gallbladder", "Agenesis of gallbladder", "GALLBLADDER, AGENESIS OF", "Gallbladder, Agenesis Of", "gallbladder, agenesis OF", "Aplasia of the gallbladder", "Agenesis of the gallbladder", "gallbladder; absence, congenital", "absence; gallbladder, congenital", "isolated agenesis of gallbladder", "Isolated agenesis of gallbladder", "Congenital absence of gallbladder", "congenital absence of gallbladder", "Agenesis of gallbladder (disorder)", "Congenital absence of gallbladder (disorder)", "congenital absence of gallbladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated agenesis of gallbladder", "shortest_name_length": 18}
{"curie": "MONDO:0017591", "names": ["CPFE", "combined pulmonary fibrosis-emphysema syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined pulmonary fibrosis-emphysema syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0948485", "names": ["Cytomegalovirus gastrointestinal infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cytomegalovirus gastrointestinal infection", "shortest_name_length": 42}
{"curie": "MONDO:0008950", "names": ["Pelizaeus-Merzbacher like brain sclerosis", "cerebral sclerosis similar to Pelizaeus-Merzbacher disease", "CEREBRAL SCLEROSIS SIMILAR TO PELIZAEUS-MERZBACHER DISEASE", "Cerebral sclerosis similar to Pelizaeus-Merzbacher disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral sclerosis similar to Pelizaeus-Merzbacher disease", "shortest_name_length": 41}
{"curie": "MONDO:0033559", "names": ["IDDSELD", "intellectual developmental disorder with seizures and language delay", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH SEIZURES AND LANGUAGE DELAY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder with seizures and language delay", "shortest_name_length": 7}
{"curie": "MONDO:0021171", "names": ["TS1", "LQT8 type 1", "Timothy syndrome type 1", "Timothy syndrome classic type", "Timothy syndrome, classic type", "Long QT syndrome with syndactyly", "Timothy syndrome type 1 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Timothy syndrome, classic type", "shortest_name_length": 3}
{"curie": "UMLS:C0851355", "names": ["Respiratory and Thoracic Disease", "Respiratory and Thoracic Disorder", "Respiratory, Thoracic, and Mediastinal Disease", "Respiratory, thoracic and mediastinal disorders", "Respiratory, Thoracic, and Mediastinal Disorder", "respiratory, thoracic, and mediastinal disorders", "respiratory, thoracic, and mediastinal disorders (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Respiratory, thoracic and mediastinal disorders", "shortest_name_length": 32}
{"curie": "MONDO:0006851", "names": ["MAS", "MECONIUM ASPIRATION", "Meconium Inhalation", "Meconium aspiration", "Meconium Aspiration", "meconium inhalation", "meconium aspiration", "aspiration meconium", "aspiration; meconium", "aspiration, meconium", "Aspiration, meconium", "inhalation; meconium", "meconium; inhalation", "meconium; aspiration", "Aspiration, Meconium", "meconium aspirations", "of meconium aspiration", "Aspiration of meconium", "aspiration of meconium", "Meconium aspiration NOS", "Meconium aspiration syndrome", "meconium aspiration syndrome", "aspiration meconium syndrome", "Meconium Aspiration Syndrome", "Syndrome, Meconium Aspiration", "aspiration; newborn, meconium", "syndrome, meconium aspiration", "Aspiration Syndrome, Meconium", "aspiration syndrome, meconium", "neonatal aspiration of meconium", "Neonatal Aspiration of Meconium", "Neonatal aspiration of meconium", "Meconium aspiration syndrome NOS", "aspiration of meconium (diagnosis)", "MAS - meconium aspiration syndrome", "MAS - Meconium aspiration syndrome", "Meconium aspiration syndrome (disorder)", "Meconium aspiration syndrome of newborn", "meconium aspiration syndrome (diagnosis)", "aspiration; syndrome of newborn, meconium", "Neonatal aspiration of meconium (disorder)", "syndrome; aspiration, of newborn, meconium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "meconium aspiration syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0012350", "names": ["C3G1", "CFHD", "CFH DEFICIENCY", "CFH Deficiency", "Cfh deficiency", "C3 GLOMERULOPATHY 1", "Factor H deficiency", "FACTOR H DEFICIENCY", "factor H deficiency", "Factor H Deficiency", "C3G1 C3 glomerulopathy 1", "complement factor H deficiency", "Factor H deficiency (disorder)", "COMPLEMENT FACTOR H DEFICIENCY", "Complement Factor H Deficiency", "Factor H deficiency (diagnosis)", "C3G-1 Complement 3 Glomerulopathy 1", "Immunodeficiency with factor H anomaly", "MPGN II with Complement Factor H Deficiency", "Glomerulonephritis With Isolated C3 Deposits And Factor H Deficiency", "Membranoproliferative Glomerulonephritis, Type II, With Complement Factor H Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complement factor H deficiency", "shortest_name_length": 4}
{"curie": "UMLS:C0751456", "names": ["Developmental Psychomotor Disorder", "Psychomotor Disorder, Developmental", "Developmental Psychomotor Disorders", "Psychomotor Disorders, Developmental"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Developmental Psychomotor Disorders", "shortest_name_length": 34}
{"curie": "UMLS:C4324706", "names": ["Bacterial vulvovaginitis", "Vaginal bacterial infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bacterial vulvovaginitis", "shortest_name_length": 24}
{"curie": "MONDO:0007607", "names": ["BHD", "BHD syndrome", "Birt-Hogg-Dube syndrome", "BIRT-HOGG-DUBE SYNDROME", "Birt-Hogg-Dubé Syndrome", "birt hogg dube syndrome", "Birt-Hogg-Dube Syndrome", "Birt-Hogg-Dubé syndrome", "Birt Hogg Dube syndrome", "birt-hogg-dube syndrome", "Birt Hogg Dube Syndrome", "Multiple fibrofolliculomas", "multiple fibrofolliculomas", "Multiple fibrofolliculomata", "Hornstein-Knickenberg Syndrome", "HORNSTEIN-KNICKENBERG SYNDROME", "Hornstein-Knickenberg syndrome", "Hornstein-Birt-Hogg-Dubé Syndrome", "Familial multiple fibrofolliculoma", "Birt-Hogg-Dube syndrome (diagnosis)", "Multiple fibrofolliculomas (disorder)", "Fibrofolliculomas with Trichodiscomas and Acrochordons", "fibrofolliculomas with trichodiscomas and acrochordons", "FIBROFOLLICULOMAS WITH TRICHODISCOMAS AND ACROCHORDONS", "Fibrofolliculomas with trichodiscomas and acrochordons"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Birt-Hogg-Dube syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C5447984", "names": ["Breast Classic Lobular Carcinoma In Situ Type A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Classic Lobular Carcinoma In Situ Type A", "shortest_name_length": 47}
{"curie": "MONDO:0001239", "names": ["AOP", "prematurity; anemia", "anemia; prematurity", "Anemia of Prematurity", "anemia of prematurity", "Anemia of prematurity", "Anaemia of prematurity", "Anemia of prematurity (disorder)", "anemia of prematurity (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anemia of prematurity", "shortest_name_length": 3}
{"curie": "UMLS:C0271767", "names": ["Neonatal Graves Disease", "disease graves neonatal", "Neonatal Graves' disease", "diseases graves neonatal", "neonatal graves' disease", "Neonatal Graves' disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neonatal Graves' disease", "shortest_name_length": 23}
{"curie": "UMLS:C1709246", "names": ["NON-NEOPLASTIC", "Non-Neoplastic Disease", "Non-Neoplastic Disorder", "Non-neoplastic Disorder", "Non-neoplastic disorder, NOS", "Non-neoplastic condition, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Disorder", "shortest_name_length": 14}
{"curie": "MONDO:0011207", "names": ["XANTHOMATOSIS, SUSCEPTIBILITY TO", "xanthomatosis, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "xanthomatosis, susceptibility to", "shortest_name_length": 32}
{"curie": "MONDO:0003618", "names": ["PYOSALPINX", "Pyosalpinx", "pyosalpinx", "Pyosalpingitis", "pyosalpingitis", "Pyosalpinx (disorder)", "pyosalpinx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyosalpinx", "shortest_name_length": 10}
{"curie": "UMLS:C4085580", "names": ["CPS I Deficiency", "CPS 1 Deficiency", "CPS 1 Deficiencies", "CPS I Deficiencies", "Carbamoyl Phosphate Synthase 1 Deficiency", "Carbamoyl Phosphate Synthetase I Deficiency", "Carbamyl Phosphate Synthetase (CPS) Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carbamoyl Phosphate Synthase 1 Deficiency", "shortest_name_length": 16}
{"curie": "MONDO:0000138", "names": ["metaphyseal dysostosis", "Metaphyseal dysostosis", "Metaphyseal chondrodysplasia", "metaphyseal chondrodysplasia", "metaphyseal chondrodysplasia (disease)", "Metaphyseal chondrodysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metaphyseal chondrodysplasia", "shortest_name_length": 22}
{"curie": "MONDO:0017487", "names": ["radial hemimelia, bilateral", "radial longitidinal meromelia, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radial hemimelia, bilateral", "shortest_name_length": 27}
{"curie": "OMIM:613463", "names": ["FGQTL5", "FASTING PLASMA GLUCOSE LEVEL QUANTITATIVE TRAIT LOCUS 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 6}
{"curie": "MONDO:0012944", "names": ["SHFLD3", "CHROMOSOME 17p13.3, TELOMERIC, DUPLICATION SYNDROME", "chromosome 17P13.3, telomeric, duplication syndrome", "Split-Hand-Foot Malformation With Long Bone Deficiency 3", "SPLIT-HAND/FOOT MALFORMATION WITH LONG BONE DEFICIENCY 3", "split-hand/foot malformation with long bone deficiency 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 17P13.3, telomeric, duplication syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C1264517", "names": ["Posttraumatic Wound Infection", "Post-traumatic wound infection", "wound infection post-traumatic", "Infection;wound;post-traumatic", "Post Traumatic Wound Infection", "post-traumatic wound infection", "wound infection; post-traumatic", "post-traumatic; wound infection", "Post-traumatic wound infection (disorder)", "Post-traumatic wound infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post-traumatic wound infection", "shortest_name_length": 29}
{"curie": "UMLS:C4518570", "names": ["Aggressive papillary tumor", "Aggressive Papillary Tumor", "Aggressive papillary tumour", "Aggressive papillary tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aggressive papillary tumor", "shortest_name_length": 26}
{"curie": "MONDO:0001049", "names": ["Dressler", "DRESSLER SYNDROME", "dressler syndrome", "Dressler syndrome", "dresslers syndrome", "Dresslers syndrome", "dressler's syndrome", "Dressler's syndrome", "postmyocardial infarct syndrom", "Postmyocardial infarct syndrom", "Dressler's syndrome (diagnosis)", "POSTMYOCARDIAL INFARCTION SYNDROME", "postmyocardial infarction syndrome", "Postmyocardial infarction syndrome", "Myocardial postinfarction syndrome", "Post-myocardial infarction syndrome", "Post myocardial infarction syndrome", "syndrome; postmyocardial infarction", "postmyocardial infarction; syndrome", "Postmyocardial infarction pericarditis", "Delayed postmyocardial infarction syndrome", "Postmyocardial infarction syndrome (disorder)", "Delayed postmyocardial infarction pericarditis", "delayed postmyocardial infarction pericarditis", "Delayed postmyocardial infarction pericarditis (disorder)", "delayed postmyocardial infarction pericarditis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dressler syndrome", "shortest_name_length": 8}
{"curie": "UMLS:C4553880", "names": ["Stage IVA Thyroid Gland Anaplastic Carcinoma AJCC v8", "Undifferentiated (Anaplastic) Stage IVA Thyroid Gland Cancer", "Stage IVA Thyroid Gland Undifferentiated (Anaplastic) Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Thyroid Gland Undifferentiated (Anaplastic) Carcinoma AJCC v8", "shortest_name_length": 52}
{"curie": "MONDO:0030069", "names": ["HIES5", "HYPER-IgE RECURRENT INFECTION SYNDROME 5, AUTOSOMAL RECESSIVE", "hyper-IgE recurrent infection syndrome 5, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyper-IgE recurrent infection syndrome 5, autosomal recessive", "shortest_name_length": 5}
{"curie": "UMLS:C1511098", "names": ["Benign Ovarian Clear Cell Tumor", "Benign Ovarian Clear Cell Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Ovarian Clear Cell Tumor", "shortest_name_length": 31}
{"curie": "MONDO:0010364", "names": ["Aldred syndrome", "Chromosome Xp11.3 Deletion Syndrome", "chromosome Xp11.3 deletion syndrome", "CHROMOSOME Xp11.3 DELETION SYNDROME", "chromosome xp11.3 microdeletion syndrome", "Chromosome Xp11.3 microdeletion syndrome", "Chromosome Xp11.3 microdeletion syndrome (disorder)", "chromosome xp11.3 microdeletion syndrome (diagnosis)", "X-linked mental handicap-retinitis pigmentosa syndrome", "chromosome xp11.3 deletion syndrome, X-linked recessive", "mental retardation, X-linked, with retinitis pigmentosa", "Mental Retardation, X-Linked, With Retinitis Pigmentosa", "MENTAL RETARDATION, X-LINKED, WITH RETINITIS PIGMENTOSA", "intellectual disability, X-linked, with retinitis pigmentosa", "X-linked intellectual disability-retinitis pigmentosa syndrome", "nonspecific mental retardation associated with retinitis pigmentosa", "Nonspecific mental retardation associated with retinitis pigmentosa", "Retinitis pigmentosa and intellectual disability due to del(X)(p11.3)", "retinitis pigmentosa and intellectual disability due to del(X)(p11.3)", "Retinitis pigmentosa and intellectual disability due to monosomy Xp11.3", "retinitis pigmentosa and intellectual disability due to monosomy Xp11.3", "nonspecific intellectual disability associated with retinitis pigmentosa", "retinitis pigmentosa and intellectual disability due to Xp11.3 microdeletion", "Retinitis pigmentosa and intellectual disability due to Xp11.3 microdeletion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability-retinitis pigmentosa syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0700033", "names": ["complete trisomy 13"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complete trisomy 13", "shortest_name_length": 19}
{"curie": "UMLS:C1336207", "names": ["Stage IIIA Gastric Cancer", "Gastric Cancer Stage IIIA", "Stage IIIA Stomach Carcinoma", "Gastric Carcinoma Stage IIIA", "Stomach Carcinoma Stage IIIA", "Stage IIIA Gastric Carcinoma", "Stage IIIA Carcinoma of Stomach", "Carcinoma of Stomach Stage IIIA", "Stage IIIA Gastric Cancer AJCC v7", "Stage IIIA Gastric (Stomach) Cancer", "Stage IIIA Carcinoma of the Stomach", "Carcinoma of the Stomach Stage IIIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Gastric Carcinoma", "shortest_name_length": 25}
{"curie": "UMLS:C0220620", "names": ["GCT", "GI Carcinoid Tumor", "GI carcinoid tumor", "Gastrointestinal NET G1", "Digestive Carcinoid Tumor", "Carcinoid Tumor of GI System", "Gastrointestinal Carcinoid Tumor", "Gastrointestinal carcinoid tumor", "gastrointestinal carcinoid tumor", "Digestive System Carcinoid Tumor", "Carcinoid Tumor of the GI System", "carcinoid tumor, gastrointestinal", "carcinoid gastrointestinal tumors", "Gastrointestinal carcinoid tumour", "Carcinoid Tumor of Digestive System", "Carcinoid Tumor of the Digestive System", "Gastrointestinal System Carcinoid Tumor", "Digestive System Neuroendocrine Tumor G1", "Gastrointestinal Neuroendocrine Tumor G1", "Carcinoid tumor of gastrointestinal tract", "Carcinoid Tumor of Gastrointestinal System", "Carcinoid tumour of gastrointestinal tract", "Carcinoid tumor of the gastrointestinal tract", "Carcinoid tumour of the gastrointestinal tract", "Carcinoid Tumor of the Gastrointestinal System", "neoplasm of gastrointestinal tract carcinoid tumor", "Carcinoid tumor of gastrointestinal tract (disorder)", "Carcinoid tumor of gastrointestinal tract (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal Carcinoid Tumor", "shortest_name_length": 3}
{"curie": "MONDO:0004207", "names": ["Pulmonary Artery Leiomyosarcoma", "pulmonary artery leiomyosarcoma", "Leiomyosarcoma of Pulmonary Artery", "leiomyosarcoma of pulmonary artery", "Leiomyosarcoma of the Pulmonary Artery", "leiomyosarcoma of the pulmonary artery"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary artery leiomyosarcoma", "shortest_name_length": 31}
{"curie": "UMLS:C5420389", "names": ["Non-Neoplastic Gingival Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Gingival Disorder", "shortest_name_length": 32}
{"curie": "MONDO:0013182", "names": ["Dup(17)(p13.3)", "dup(17)(p13.3)", "trisomy 17p13.3", "Trisomy 17p13.3", "17p13.3 duplication syndrome", "17p13.3 microduplication syndrome", "chromosome 17p13.3 duplication syndrome", "Chromosome 17p13.3 Duplication Syndrome", "17p13.3 microduplication syndrome (disorder)", "chromosome 17p13.3 centromeric duplication syndrome", "CHROMOSOME 17p13.3, CENTROMERIC, DUPLICATION SYNDROME", "chromosome 17p13.3, centromeric, DUPLICATION syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 17p13.3 duplication syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C5575348", "names": ["Isomorphic Diffuse Glioma", "Isomorphic Astrocytoma Variant", "Diffuse Astrocytoma, MYB-Altered"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse Astrocytoma, MYB-Altered", "shortest_name_length": 25}
{"curie": "UMLS:C0333886", "names": ["Moderate urothelial cell atypia", "Moderate Transitional Cell Atypia", "Moderate transitional cell atypia", "Moderate transitional cell atypia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Moderate transitional cell atypia", "shortest_name_length": 31}
{"curie": "MONDO:0035472", "names": ["GJC2-related late-onset primary lymphedema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "GJC2-related late-onset primary lymphedema", "shortest_name_length": 42}
{"curie": "UMLS:C0431415", "names": ["Lumbosacral agenesis", "Lumbosacral agenesis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lumbosacral agenesis", "shortest_name_length": 20}
{"curie": "UMLS:C5418916", "names": ["Unresectable Primary Peritoneal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Primary Peritoneal Carcinoma", "shortest_name_length": 41}
{"curie": "UMLS:C5555066", "names": ["Primary Central Atypical Cartilaginous Tumor/Chondrosarcoma, Grade 1", "Primary Conventional Central Atypical Cartilaginous Tumor/Chondrosarcoma, Grade 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Central Atypical Cartilaginous Tumor/Chondrosarcoma, Grade 1", "shortest_name_length": 68}
{"curie": "UMLS:C0086432", "names": ["Segmental Hyalinosis", "Segmental hyalinosis", "HYALINOSIS, SEGMENTAL", "Hyalinosis, Segmental", "Segmental Glomerular Hyalinosis", "Glomerular Hyalinosis, Segmental", "Hyalinosis, Segmental Glomerular"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyalinosis, Segmental Glomerular", "shortest_name_length": 20}
{"curie": "UMLS:C1708554", "names": ["Intraocular Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraocular Infection", "shortest_name_length": 21}
{"curie": "UMLS:C1142523", "names": ["Hypothrombinemia", "Hypothrombinaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypothrombinaemia", "shortest_name_length": 16}
{"curie": "UMLS:C0080203", "names": ["tachyrhythmia", "Tachyarrhythmia", "TACHYARRHYTHMIA", "tachyarrhythmia", "tachyarrhythmias", "Tachyarrhythmias", "Tachyarrhythmia, NOS", "Tachyarrhythmia (disorder)", "rapid and irregular heartbeat"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tachyarrhythmia", "shortest_name_length": 13}
{"curie": "UMLS:C1112353", "names": ["Medical device complication", "complications of medical devices"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Medical device complication", "shortest_name_length": 27}
{"curie": "MONDO:0013725", "names": ["HNPCC7", "MLH3 hereditary nonpolyposis colon cancer", "hereditary nonpolyposis colorectal cancer type 7", "colorectal cancer, hereditary nonpolyposis, type 7", "Colorectal Cancer, Hereditary Nonpolyposis, Type 7", "COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 7", "COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 7 (disorder)", "hereditary nonpolyposis colon cancer caused by mutation in MLH3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorectal cancer, hereditary nonpolyposis, type 7", "shortest_name_length": 6}
{"curie": "MONDO:0016162", "names": ["bilateral frontal polymicrogyria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bilateral frontal polymicrogyria", "shortest_name_length": 32}
{"curie": "UMLS:C4521871", "names": ["Stage 0 Pancreatic Cancer", "stage 0 pancreatic cancer", "stage 0 pancreatic cancer AJCC v8", "Stage 0 Pancreatic Cancer AJCC v8", "stage 0 exocrine pancreatic cancer AJCC v8", "Stage 0 Exocrine Pancreatic Cancer AJCC v8", "stage 0 exocrine pancreatic carcinoma AJCC v8", "Stage 0 Exocrine Pancreatic Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Pancreatic Cancer AJCC v8", "shortest_name_length": 25}
{"curie": "UMLS:C1336485", "names": ["Stage I Subdiaphragmatic Nodular Lymphocyte Predominant Hodgkin Lymphoma", "Stage I Subdiaphragmatic Nodular Lymphocyte Predominant Hodgkin's Lymphoma", "Subdiaphragm Stage I Hodgkin's Lymphoma Nodular Lymphocyte Predominance Type", "Stage I Subdiaphragmatic Hodgkin's Disease Nodular Lymphocyte Predominance Type", "Stage I Subdiaphragmatic Hodgkin's Lymphoma Nodular Lymphocyte Predominant Type", "Ann Arbor Stage I Subdiaphragmatic Nodular Lymphocyte Predominant Hodgkin Lymphoma", "Stage I Hodgkin's Disease Nodular Lymphocyte Predominance Type below the Diaphragm", "Stage I Hodgkin's Lymphoma Nodular Lymphocyte Predominance Type below the Diaphragm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage I Subdiaphragmatic Nodular Lymphocyte Predominant Hodgkin Lymphoma", "shortest_name_length": 72}
{"curie": "MONDO:0021040", "names": ["pancreas", "pancreas ca", "tumor pancreas", "PANCREAS TUMOR", "Pancreas Tumor", "pancreas tumor", "Pancreas Cancer", "pancreas tumors", "tumour pancreas", "PANCREAS CANCER", "pancreas cancer", "Pancreas cancer", "pancreas tumour", "Pancreatic tumor", "Pancreas Cancers", "Pancreas--Cancer", "Pancreas--Tumors", "Cancer, Pancreas", "Pancreatic Tumor", "pancreatic tumor", "Pancreatic cancer", "Tumor of pancreas", "Cancers, Pancreas", "Pancreatic tumour", "Pancreatic Cancer", "pancreatic tumors", "tumor of pancreas", "neoplasm pancreas", "pancreas neoplasm", "pancreatic cancer", "Pancreas Neoplasm", "Tumor of Pancreas", "Cancer of Pancreas", "Pancreatic Cancers", "Cancer of pancreas", "Pancreas Neoplasms", "Tumour of pancreas", "neoplasms pancreas", "Neoplasm, Pancreas", "pancreatic cancers", "Cancer, Pancreatic", "Neoplasms, Pancreas", "Cancers, Pancreatic", "pancreatic neoplasm", "Pancreatic neoplasm", "Pancreatic Neoplasm", "Pancreatic neoplasms", "Neoplasm of pancreas", "Neoplasm, Pancreatic", "pancreatic neoplasms", "neoplasm of pancreas", "Neoplasm of Pancreas", "Pancreatic Neoplasms", "Neoplasms, Pancreatic", "tumor of the pancreas", "Tumor of the Pancreas", "Pancreas neoplasm NOS", "CA - Pancreatic cancer", "Cancer of the Pancreas", "cancer of the pancreas", "Cancer of the pancreas", "tumor pancreatic cancer", "CA - Cancer of pancreas", "Pancreatic neoplasm NOS", "Neoplasm malig;pancreas", "Neoplasm of the Pancreas", "Neoplasm of the pancreas", "neoplasm of the pancreas", "PANCREAS CANCER MALIGNANT", "Neoplasia of the pancreas", "pancreatic tumor or cancer", "malignant tumor of pancreas", "Pancreas neoplasm malignant", "Malignant tumor of pancreas", "PANCREAS NEOPLASM MALIGNANT", "Malignant neoplasm pancreas", "pancreas neoplasm (disease)", "Malignant tumour of pancreas", "malignant pancreatic neoplasm", "Malignant Pancreatic Neoplasm", "Malignant neoplasm of pancreas", "malignant neoplasm of pancreas", "Malignant Neoplasm of Pancreas", "Neoplasm of pancreas (disorder)", "neoplasm of pancreas (diagnosis)", "Malignant Neoplasm of the Pancreas", "Malignant neoplasm of pancreas, NOS", "Increased risk of pancreatic cancer", "increased risk of pancreatic cancer", "malignant neosplasm of the pancreas", "Malignant tumor of pancreas (disorder)", "malignant neoplasm of pancreas (diagnosis)", "Malignant neoplasm of pancreas, unspecified", "Malignant neoplasm of pancreas, part unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic neoplasm", "shortest_name_length": 8}
{"curie": "MONDO:0014323", "names": ["RP68", "RETINITIS PIGMENTOSA 68", "retinitis pigmentosa 68", "SLC7A14 retinitis pigmentosa", "retinitis pigmentosa type 68", "retinitis pigmentosa caused by mutation in SLC7A14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 68", "shortest_name_length": 4}
{"curie": "MONDO:0006009", "names": ["Viral encephalitis", "Encephalitis viral", "Viral Encephalitis", "viral encephalitis", "encephalitis viral", "encephalitis; viral", "Encephalitis, viral", "Encephalitis, Viral", "viral; encephalitis", "Viruses encephalitis", "epidemic encephalitis", "Encephalitis viral NOS", "Viral encephalitis, NOS", "Viruses caused encephalitis", "Viral encephalitis (disorder)", "viral encephalitis (diagnosis)", "Unspecified viral encephalitis", "Viral Infectious Encephalomyelitis", "Infectious Encephalomyelitis, Viral", "Encephalomyelitis, Viral Infectious", "Encephalomyelitis, Infectious, Viral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "viral encephalitis", "shortest_name_length": 18}
{"curie": "MONDO:0015524", "names": ["Serrated polyposis", "serrated polyposis", "Serrated intestinal polyps", "Serrated polyposis syndrome", "Colorectal Serrated Polyposis", "hyperplastic polyposis syndrome", "Hyperplastic Polyposis Syndrome", "Hyperplastic polyposis syndrome", "Colorectal Serrated Polyposis Syndrome", "Hyperplastic polyposis syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperplastic polyposis syndrome", "shortest_name_length": 18}
{"curie": "MONDO:0001554", "names": ["phacogenic glaucoma", "phacomorphic glaucoma", "Phacomorphic glaucoma", "Lens swelling glaucoma", "lens swelling glaucoma", "Phacomorphic glaucoma (disorder)", "Lens induced angle closure glaucoma", "lens induced angle closure glaucoma", "Glaucoma associated with other lens disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phacogenic glaucoma", "shortest_name_length": 19}
{"curie": "UMLS:C1167738", "names": ["Small Intestine Cancer Stage IV", "Stage IV Small Intestinal Cancer", "Stage IV Small Intestine Carcinoma", "Small intestine carcinoma stage IV", "Stage IV Small Intestinal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small intestine carcinoma stage IV", "shortest_name_length": 31}
{"curie": "UMLS:C0855112", "names": ["Diffuse Large B-Cell Lymphoma Refractory", "Refractory Diffuse Large B-Cell Lymphoma", "Diffuse large B-cell lymphoma refractory"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse large B-cell lymphoma refractory", "shortest_name_length": 40}
{"curie": "MONDO:0002070", "names": ["vsd", "VSD", "Ventriculoseptal defect", "Ventricular Septal Defect", "ventricular septal defect", "Defect;ventricular septal", "Ventricular septal defect", "VENTRICULAR SEPTAL DEFECT", "Ventricular septal defects", "Ventricular Septal Defects", "ventricular; septal defect", "Defect, Ventricular Septal", "ventricular septal defects", "Septal Defect, Ventricular", "defect; ventricular septal", "septum; defect, ventricular", "Septal Defects, Ventricular", "defect; septum, ventricular", "Ventricular septal defect NOS", "Interventricular septal defect", "Intraventricular Septal Defect", "interventricular communication", "DEFECT INTERVENTRICULAR SEPTUM", "Septum interventricular patent", "SEPTUM INTERVENTRICULAR PATENT", "Ventricular septal abnormality", "Defect interventricular septum", "interventricular septal defect", "ventricular septal abnormality", "Defect, Intraventricular Septal", "defect; interventricular septal", "Ventricular Septal Defect (VSD)", "Ventricular septal defect (VSD)", "Intraventricular Septal Defects", "VSD (ventricular septal defect)", "Septal Defect, Intraventricular", "interventricular septal; defect", "VSD - Ventricular septal defect", "Defects, Intraventricular Septal", "Septal Defects, Intraventricular", "heart septal defects, ventricular", "Heart Septal Defects, Ventricular", "anomaly; heart, septum, ventricular", "heart; anomaly, septum, ventricular", "ventricular septal defect (disease)", "Ventricular septal defect (disorder)", "Congenital ventricular septal defect", "VENTRICULAR SEPTAL DEFECT CONGENITAL", "ventricular septal defect (diagnosis)", "closure; incomplete, septum, ventricular", "incomplete; closure, septum, ventricular", "Ventricular septal abnormality (disorder)", "ventricular septal abnormality (diagnosis)", "closure; incomplete, septum, interventricular", "incomplete; closure, septum, interventricular", "Congenital ventricular septal defect (disorder)", "Hole in heart wall separating two lower heart chambers"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ventricular septal defect", "shortest_name_length": 3}
{"curie": "MONDO:0012798", "names": ["DEAFNESS, UNILATERAL, WITH DELAYED ENDOLYMPHATIC HYDROPS", "Deafness, Unilateral, With Delayed Endolymphatic Hydrops", "deafness, unilateral, with delayed endolymphatic hydrops"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness, unilateral, with delayed endolymphatic hydrops", "shortest_name_length": 56}
{"curie": "MONDO:0035117", "names": ["PUM1-associated developmental disability-ataxia-seizure syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PUM1-associated developmental disability-ataxia-seizure syndrome", "shortest_name_length": 64}
{"curie": "MONDO:0006301", "names": ["Embryonal adenoma", "Metanephric adenoma", "Metanephric Adenoma", "metanephric adenoma", "Kidney Embryonal Adenoma", "Metanephric adenoma (morphologic abnormality)", "metanephric adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metanephric adenoma", "shortest_name_length": 17}
{"curie": "UMLS:C1517126", "names": ["Fallopian Tube Soft Tissue Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fallopian Tube Soft Tissue Neoplasm", "shortest_name_length": 35}
{"curie": "UMLS:C5575717", "names": ["Dactylomegaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dactylomegaly", "shortest_name_length": 13}
{"curie": "UMLS:C0334427", "names": ["Regressing Melanoma", "Regressing Malignant Melanoma", "Regressing malignant melanoma", "Malignant melanoma, regressing", "[M] Malignant melanoma, regressing", "Malignant melanoma, regressing (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant melanoma, regressing", "shortest_name_length": 19}
{"curie": "MONDO:0007948", "names": ["MARFANOID HYPERMOBILITY SYNDROME", "marfanoid hypermobility syndrome", "Marfanoid hypermobility syndrome", "Marfanoid joint hypermobility syndrome", "Marfanoid joint hypermobility syndrome (disorder)", "Marfanoid joint hypermobility syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "marfanoid hypermobility syndrome", "shortest_name_length": 32}
{"curie": "MONDO:0017366", "names": ["SDHx-Related Syndromes", "SDH Deficient Tumor Syndrome", "Familial Paraganglioma Syndrome", "familial pheochromocytoma-paraganglioma", "hereditary pheochromocytoma-paraganglioma", "hereditary paraganglioma-pheochromocytoma", "SDHx-related paraganglioma-pheochromocytoma", "Familial Paraganglioma-Pheochromocytoma Syndrome", "Hereditary Paraganglioma-Pheochromocytoma Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary pheochromocytoma-paraganglioma", "shortest_name_length": 22}
{"curie": "MONDO:0004101", "names": ["multicentric papillary thyroid carcinoma", "Multicentric Papillary Thyroid Carcinoma", "Multicentric Thyroid Gland Papillary Carcinoma", "Multicentric Papillary Thyroid Gland Carcinoma", "multicentric papillary thyroid gland carcinoma", "multicentric thyroid gland papillary carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multicentric papillary thyroid carcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0054716", "names": ["MCPH19", "primary autosomal recessive microcephaly 19", "microcephaly 19, primary, autosomal recessive", "microcephaly 19, PRIMARY, autosomal recessive", "MICROCEPHALY 19, PRIMARY, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly 19, primary, autosomal recessive", "shortest_name_length": 6}
{"curie": "MONDO:0044765", "names": ["SRNS", "NPHS2", "Nephrotic Syndrome-Steroid-Resistant", "Steroid-resistant nephrotic syndrome", "Steroid Resistant Nephrotic Syndrome", "nephrotic syndrome congenital type 2", "nephrotic syndrome steroid-resistant", "Steroid-Resistant Nephrotic Syndrome", "nephrotic syndrome-steroid-resistant", "steroid-resistant nephrotic syndrome", "Nephrotic syndrome, steroid-resistant", "Nephrotic Syndrome, Steroid-Resistant", "Steroid-Resistant Nephrotic Syndromes", "Steroid-unresponsive nephrotic syndrome", "steroid-unresponsive nephrotic syndrome", "SRNS - Steroid-resistant nephrotic syndrome", "SRNS - steroid-resistant nephrotic syndrome", "Steroid-resistant nephrotic syndrome (disorder)", "nephrotic syndrome congenital type 2 (diagnosis)", "Steroid-resistant nephrotic syndrome (diagnosis)", "Steroid resistant nephrotic syndrome of childhood", "nephrotic syndrome, idiopathic, steroid-resistant", "nephrotic syndrome of childhood - steroid resistant", "Nephrotic Syndrome of Childhood - Steroid Resistant", "nephrotic syndrome, steroid-resistant, autosomal recessive", "Steroid resistant nephrotic syndrome of childhood (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "steroid-resistant nephrotic syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0000938", "names": ["leiomyoma stomach", "GASTRIC LEIOMYOMA", "stomach leiomyoma", "Gastric Leiomyoma", "gastric leiomyoma", "Gastric leiomyoma", "gastric leiomyomas", "STOMACH, LEIOMYOMA", "Leiomyoma of stomach", "leiomyoma of stomach", "Leiomyoma of Stomach", "Leiomyoma of the Stomach", "leiomyoma of the stomach", "benign gastric leiomyoma", "benign leiomyoma of stomach", "benign leiomyomas of stomach", "Leiomyoma of stomach (disorder)", "benign leiomyoma of stomach (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric leiomyoma", "shortest_name_length": 17}
{"curie": "UMLS:C4524742", "names": ["Pathologic Stage IVB Gastroesophageal Junction Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IVB Gastroesophageal Junction Adenocarcinoma AJCC v8", "shortest_name_length": 69}
{"curie": "MONDO:0043191", "names": ["Bruce winship syndrome", "Bruce Winship syndrome", "Radial defect Robin sequence", "radial defect robin sequence", "bilateral radial defects club foot deformity micrognathia and cleft palate", "Bilateral radial defects, club foot deformity, micrognathia and cleft palate", "bilateral radial defects, club foot deformity, micrognathia and cleft palate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radial defect robin sequence", "shortest_name_length": 22}
{"curie": "MONDO:0100482", "names": ["XDR-TB", "Extensively Drug-Resistant TB", "Extreme drug resistant tuberculosis", "Extremely Drug-Resistant Tuberculoses", "Extremely Drug Resistant Tuberculosis", "Extremely drug resistant tuberculosis", "extremely drug-resistant tuberculosis", "Extremely Drug-Resistant Tuberculosis", "Tuberculoses, Extremely Drug-Resistant", "Drug-Resistant Tuberculosis, Extremely", "Tuberculosis, Extremely Drug-Resistant", "Tuberculosis, Extremely Drug Resistant", "Drug-Resistant Tuberculoses, Extremely", "Extensively Drug Resistant Tuberculosis", "Extensively Drug-Resistant Tuberculosis", "Extensively drug resistant tuberculosis", "tuberculosis drug-resistant extensively", "extensively drug-resistant tuberculosis", "Extensively Drug-Resistant Tuberculoses", "Drug-Resistant Tuberculosis, Extensively", "Drug-Resistant Tuberculoses, Extensively", "Tuberculoses, Extensively Drug-Resistant", "Tuberculosis, Extensively Drug-Resistant", "Tuberculosis, Extensively Drug Resistant", "Extreme drug resistant tuberculosis (disorder)", "extremely drug-resistant tuberculosis (diagnosis)", "Extensively drug resistant tuberculosis (disorder)", "extensively drug-resistant tuberculosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extensively drug-resistant tuberculosis", "shortest_name_length": 6}
{"curie": "MONDO:0024229", "names": ["miliaria crystallina"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "miliaria crystallina", "shortest_name_length": 20}
{"curie": "MONDO:0017075", "names": ["upper thoracic spina bifida cystica"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "upper thoracic spina bifida cystica", "shortest_name_length": 35}
{"curie": "MONDO:0044881", "names": ["hematologic cancer", "Hematologic Cancer", "hematopoietic tumor", "hematological tumor", "Hematopoietic Cancer", "hematologic neoplasm", "Hematologic Neoplasm", "hematopoietic cancer", "Hematopoietic Neoplasm", "hematopoietic neoplasm", "Hematologic Malignancy", "hematologic malignancy", "Hematological Neoplasm", "hematological neoplasm", "hematopoietic cell tumor", "Hematopoietic malignancy, NOS", "hematopoietic malignancy, NOS", "malignant hematologic neoplasm", "Malignant Hematologic Neoplasm", "Malignant Hematopoietic Neoplasm", "hematopoietic, Including myeloma", "malignant hematopoietic neoplasm", "Hematopoietic and Lymphoid Neoplasm", "HEMOLYMPHORETICULAR tumor, malignant", "hematopoietic and lymphoid neoplasms", "HEMOLYMPHORETICULAR TUMOR, MALIGNANT", "Hematopoietic and Lymphoid Cell Neoplasm", "hematopoietic and lymphoid cell neoplasm", "Hematopoietic Neoplasms Including Lymphomas", "hematopoietic neoplasms including lymphomas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hematopoietic and lymphoid cell neoplasm", "shortest_name_length": 18}
{"curie": "MONDO:0014882", "names": ["SPG77", "hereditary spastic paraplegia 77", "FARS2 hereditary spastic paraplegia", "hereditary spastic paraplegia type 77", "autosomal recessive spastic paraplegia 77", "spastic paraplegia 77, autosomal recessive", "SPASTIC PARAPLEGIA 77, AUTOSOMAL RECESSIVE", "Autosomal recessive spastic paraplegia type 77", "autosomal recessive spastic paraplegia type 77", "Autosomal recessive spastic paraplegia type 77 (disorder)", "hereditary spastic paraplegia caused by mutation in FARS2", "autosomal recessive spastic paraplegia type 77 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 77", "shortest_name_length": 5}
{"curie": "MONDO:0013197", "names": ["CMH14", "hypertrophic cardiomyopathy 14", "cardiomyopathy, hypertrophic, 14", "MYH6 hypertrophic cardiomyopathy", "hypertrophic cardiomyopathy type 14", "cardiomyopathy familial hypertrophic 14", "CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 14", "Cardiomyopathy, Familial Hypertrophic, 14", "cardiomyopathy, familial hypertrophic, 14", "Familial Hypertrophic Cardiomyopathy Type 14", "cardiomyopathy, familial hypertrophic, type 14", "hypertrophic cardiomyopathy caused by mutation in MYH6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophic cardiomyopathy 14", "shortest_name_length": 5}
{"curie": "MONDO:0004796", "names": ["meningitis", "Infective Meningitis", "infective meningitis", "Infective meningitis", "Infectious meningitis", "Infectious Meningitis", "infectious meningitis", "Infective meningitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infectious meningitis", "shortest_name_length": 10}
{"curie": "UMLS:C5555126", "names": ["Recurrent Aggressive B-Cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Aggressive B-Cell Non-Hodgkin Lymphoma", "shortest_name_length": 48}
{"curie": "UMLS:C0345531", "names": ["Upper Gum Carcinoma", "Carcinoma of upper gum", "Carcinoma of Upper Gum", "Upper Gingival Carcinoma", "Carcinoma of the Upper Gum", "Carcinoma of Upper Gingiva", "Carcinoma of the Upper Gingiva", "Carcinoma of upper gum (disorder)", "Carcinoma of upper gum (diagnosis)", "gum neoplasm malignant carcinoma of upper gum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carcinoma of upper gum", "shortest_name_length": 19}
{"curie": "UMLS:C4525398", "names": ["II", "Stage II Distal Bile Duct Cancer AJCC v8", "Stage II Distal Bile Duct Carcinoma AJCC v8", "Stage II Extrahepatic (Distal) Bile Duct Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Distal Bile Duct Cancer AJCC v8", "shortest_name_length": 2}
{"curie": "UMLS:C5666802", "names": ["pHGG RTK1", "Diffuse Pediatric-Type High-Grade Glioma RTK1", "Diffuse Pediatric-Type High Grade Glioma RTK1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse Pediatric-Type High Grade Glioma RTK1", "shortest_name_length": 9}
{"curie": "MONDO:0002634", "names": ["bone liposarcoma", "Bone Liposarcoma", "liposarcoma of bone", "Liposarcoma of Bone", "liposarcoma of the bone", "Liposarcoma of the bone", "bone tissue liposarcoma", "Liposarcoma of the Bone", "liposarcoma of bone tissue", "liposarcoma of bone (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "liposarcoma of bone", "shortest_name_length": 16}
{"curie": "UMLS:C4331336", "names": ["Stage IVA Hypopharyngeal Throat Cancer", "Stage IVA Hypopharyngeal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Hypopharyngeal Carcinoma AJCC v8", "shortest_name_length": 38}
{"curie": "UMLS:C4553567", "names": ["Stage III Differentiated Thyroid Gland Cancer", "Stage III Differentiated Thyroid Gland Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Differentiated Thyroid Gland Carcinoma AJCC v8", "shortest_name_length": 45}
{"curie": "MONDO:0018538", "names": ["inherited digestive cancer-predisposing syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited digestive cancer-predisposing syndrome", "shortest_name_length": 48}
{"curie": "MONDO:0003360", "names": ["SMALL BOWEL LEIOMYOSARCOMA", "Small Bowel Leiomyosarcoma", "small bowel leiomyosarcoma", "Leiomyosarcoma of Small Bowel", "leiomyosarcoma of small bowel", "Small intestine leiomyosarcoma", "Small Intestine Leiomyosarcoma", "small intestine leiomyosarcoma", "small intestinal leiomyosarcoma", "Small Intestinal Leiomyosarcoma", "leiomyosarcoma, small intestine", "INTESTINE, SMALL, LEIOMYOSARCOMA", "leiomyosarcoma of the small bowel", "leiomyosarcoma of small intestine", "Leiomyosarcoma of the Small Bowel", "leiomyosarcoma of the small Bowel", "Leiomyosarcoma of Small Intestine", "Leiomyosarcoma of small intestine", "Leiomyosarcoma of the Small Intestine", "leiomyosarcoma of the small intestine", "smooth muscle connective tissue tumor", "Leiomyosarcoma of small intestine (disorder)", "leiomyosarcoma of small intestine (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small intestine leiomyosarcoma", "shortest_name_length": 26}
{"curie": "UMLS:C1336466", "names": ["Stage I Nasal Cavity Cancer", "Stage I Nasal Cavity Carcinoma", "Stage I Carcinoma of Nasal Cavity", "Stage I Carcinoma of the Nasal Cavity", "Stage I Nasal Cavity Carcinoma AJCC v6", "Stage I Nasal Cavity Carcinoma AJCC v7", "Stage I Nasal Cavity Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Nasal Cavity Cancer AJCC v6 and v7", "shortest_name_length": 27}
{"curie": "MONDO:0005220", "names": ["BDC", "cDC", "CDC", "Bellini carcinoma", "Bellini Duct Carcinoma", "Bellini duct carcinoma", "bellini duct carcinoma", "Bellini’s duct carcinoma", "Collecting duct carcinoma", "Collecting Duct Carcinoma", "collecting duct carcinoma", "renal medullary carcinoma", "renal Medullary carcinoma", "Collecting Duct Carcinomas", "Carcinoma, Collecting Duct", "Carcinomas, Collecting Duct", "Collecting duct renal cancer", "collecting duct renal cancer", "Renal Collecting Duct Carcinoma", "Renal collecting duct carcinoma", "renal collecting duct carcinoma", "Kidney Collecting Duct Carcinoma", "kidney collecting duct carcinoma", "Collecting Duct Carcinoma (Kidney)", "carcinoma of renal collecting duct", "Carcinoma of Renal Collecting Duct", "carcinoma of renal Collecting duct", "Carcinoma of Kidney Collecting Duct", "Collecting Duct Carcinomas (Kidney)", "Collecting duct carcinoma of kidney", "collecting duct carcinoma of kidney", "Carcinoma, Collecting Duct (Kidney)", "carcinoma of kidney collecting duct", "collecting duct renal cell carcinoma", "Collecting Duct Renal Cell Carcinoma", "Carcinomas, Collecting Duct (Kidney)", "Renal carcinoma, collecting duct type", "renal carcinoma, collecting duct type", "carcinoma of the renal collecting duct", "Carcinoma of the Renal Collecting Duct", "carcinoma of the kidney collecting duct", "collecting duct carcinoma of the kidney", "Carcinoma of the Kidney Collecting Duct", "Collecting Duct Carcinoma of the Kidney", "carcinoma of collecting ducts of Bellini", "Carcinoma of Collecting Ducts of Bellini", "collecting duct of renal tubule carcinoma", "carcinoma of collecting duct of renal tubule", "carcinoma of the collecting ducts of Bellini", "Carcinoma of the collecting ducts of Bellini", "Carcinoma of the Collecting Ducts of Bellini", "Collecting duct carcinoma of kidney (disorder)", "collecting duct carcinoma of kidney (diagnosis)", "Collecting duct carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "collecting duct carcinoma", "shortest_name_length": 3}
{"curie": "MONDO:0006664", "names": ["ASD", "asd", "IA SEPTAL DEFECT", "Atrioseptal defect", "atrioseptal defect", "Atria septal defect", "Atrial Septum Defect", "Defect;atrial septal", "atrial septum defect", "Atrial septal defect", "ATRIAL SEPTAL DEFECT", "Atrial septum defect", "Atrial Septal Defect", "atrial septal defect", "Atrial septal defects", "Atrial Septal Defects", "Defect, Atrial Septal", "defect; atrial septal", "atrial septal defects", "DEFECT ARTRIAL SEPTUM", "Septal Defect, Atrial", "auricular septal defect", "Atrial septal defect NOS", "auricular septal; defect", "defect; auricular septal", "interatrial septal defect", "Septal defect interatrial", "SEPTAL DEFECT INTERATRIAL", "Interatrial septal defect", "Interatrial communication", "Atria septal defect (ASD)", "interatrial communication", "atrial septal defect (ASD)", "ASD (atrial septal defect)", "HEART SEPTAL DEFECT ATRIAL", "atrial septal heart defect", "interatrial septal; defect", "Heart septal defect atrial", "ASD - Atrial septal defect", "Atrial septal defect (ASD)", "atrial heart septal defect", "defect; interatrial septal", "Defect in the atrial septum", "atrial septal heart defects", "Interauricular communication", "Heart Septal Defects, Atrial", "interauricular communication", "Interauricular septal defect", "interauricular septal defect", "interauricular septal; defect", "defect; interauricular septal", "Atrial septal defect (disorder)", "Congenital atrial septal defect", "congenital atrial septal defect", "atrial septal defect (diagnosis)", "Atrial septal defect, unspecified", "heart; anomaly, septum, auricular", "anomaly; heart, septum, auricular", "Interauricular septal defect (disorder)", "Congenital atrial septal defect (disorder)", "incomplete; closure, septum, interauricular", "closure; incomplete, septum, interauricular", "Hole in heart wall separating two upper heart chambers", "An opening in the wall separating the top two chambers of the heart"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial septal defect", "shortest_name_length": 3}
{"curie": "MONDO:0003835", "names": ["Gastric Cardia Adenocarcinoma", "gastric cardia adenocarcinoma", "cardia of stomach adenocarcinoma", "Adenocarcinoma of Gastric Cardia", "adenocarcinoma of gastric cardia", "adenocarcinoma of cardia of stomach", "adenocarcinoma of Cardia of stomach", "Adenocarcinoma of Cardia of Stomach", "Adenocarcinoma of the Gastric Cardia", "adenocarcinoma of the gastric cardia", "Adenocarcinoma of the Cardia of the Stomach", "adenocarcinoma of the cardia of the stomach"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric cardia adenocarcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0008856", "names": ["IMD27A", "IFNGR1 Deficiency", "IFNGR 1 Deficiency", "Immunodeficiency 27A", "immunodeficiency 27A", "IMMUNODEFICIENCY 27A", "immunodeficiency type 27A", "atypical mycobacteriosis, familial", "Autosomal Recessive IFNGR1 Deficiency", "autosomal recessive IFNGR1 deficiency", "IFNGR1 deficiency, autosomal recessive", "Interferon Gamma Receptor 1 Deficiency", "IFNGR1 DEFICIENCY, AUTOSOMAL RECESSIVE", "MSMD due to Complete IFNGR1 Deficiency", "Interferon gamma, receptor 1, deficiency", "immunodeficiency 27A, mycobacteriosis, AR", "MSMD due to complete IFNgammaR1 deficiency", "MSMD due to Complete IFNgammaR1 Deficiency", "atypical mycobacterial infection, disseminated", "mycobacterial disease, Mendelian susceptibility to", "atypical mycobacterial infection, familial disseminated", "autosomal recessive immunodeficiency 27A, mycobacteriosis", "immunodeficiency 27A, Mycobacteriosis, autosomal recessive", "Autosomal Recessive Interferon Gamma Receptor 1 Deficiency", "IMMUNODEFICIENCY 27A, MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE", "MSMD due to complete interferon gamma receptor 1 deficiency", "autosomal recessive MSMD due to partial IFNgammaR1 deficiency", "autosomal recessive MSMD due to partial interferon gamma receptor 1 deficiency", "Mendelian susceptibility to mycobacterial disease due to complete IFNgammaR1 deficiency", "Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR1 deficiency", "Mendelian Susceptibility to Mycobacterial Diseases due to Complete IFNgammaR1 Deficiency", "Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency", "Mendelian susceptibility to mycobacterial diseases due to complete interferon gamma receptor 1 deficiency", "autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency", "Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency (disorder)", "Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency (diagnosis)", "autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 1 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 27A", "shortest_name_length": 6}
{"curie": "UMLS:C4288893", "names": ["Acute Biphenotypic Leukemia", "Infant Acute Biphenotypic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infant Acute Biphenotypic Leukemia", "shortest_name_length": 27}
{"curie": "MONDO:0100242", "names": ["glioma susceptibility", "glioma, susceptibility", "glioma, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glioma susceptibility", "shortest_name_length": 21}
{"curie": "MONDO:0100429", "names": ["ICP", "RICP", "pregnancy related cholestasis", "pregnancy-related cholestasis", "gravidic intrahepatic cholestasis", "intrahepatic cholestasis of pregnancy", "Intrahepatic Cholestasis of Pregnancy", "cholestasis, intrahepatic of pregnancy", "familial intrahepatic cholestasis of pregnancy", "recurrent intrahepatic cholestasis of pregnancy", "familial recurrent intrahepatic cholestasis of pregnancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intrahepatic cholestasis of pregnancy", "shortest_name_length": 3}
{"curie": "UMLS:C0267489", "names": ["Jejunal ulcer", "jejunal ulcer", "Jejunal Ulcer", "ULCER JEJUNUM", "Ulcer jejunum", "jejunal ulcers", "Ulcer of jejunum", "ULCER OF JEJUNUM", "Jejunal ulceration", "Jejunal ulcer (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jejunal ulcer", "shortest_name_length": 13}
{"curie": "UMLS:C4055251", "names": ["Childhood AML, NOS", "Childhood Acute Myeloid Leukemia, NOS", "Childhood Acute Myeloid Leukemia, NOC", "Childhood Acute Myeloid Leukemia Not Otherwise Specified", "Childhood Acute Myeloid Leukemia, Not Otherwise Specified", "Childhood Acute Myeloid Leukemia Defined by Differentiation", "Childhood Acute Myeloid Leukemia, Not Otherwise Characterized"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Acute Myeloid Leukemia Not Otherwise Specified", "shortest_name_length": 18}
{"curie": "MONDO:0008087", "names": ["HNPP", "Tomaculous neuropathy", "TOMACULOUS NEUROPATHY", "tomaculous neuropathy", "potato-grubbing palsy", "Potato-grubbing palsy", "Compression Neuropathy", "tulip-bulb digger's palsy", "Tulip-bulb digger's palsy", "familial recurrent polyneuropathy", "Polyneuropathy, familial recurrent", "POLYNEUROPATHY, FAMILIAL RECURRENT", "polyneuropathy, familial recurrent", "Heterozygous microdeletion 17p11.2p12", "heterozygous microdeletion 17p11.2p12", "current pressure-sensitive neuropathy", "Current pressure-sensitive neuropathy", "Inherited Tendency To Pressure Palsies", "Familial Pressure Sensitive Neuropathy", "hereditary liability to pressure palsies", "Hereditary liability to pressure palsies", "Hereditary Pressure Sensitive Neuropathy", "neuropathy, recurrent, with pressure palsies", "Hereditary liability to pressure palsies (disorder)", "Hereditary Neuropathy with Liability to Pressure Palsy", "hereditary neuropathy with liability to pressure palsy", "Hereditary neuropathy with liability to pressure palsies", "Hereditary Neuropathy with Liability To Pressure Palsies", "hereditary neuropathy with liability to pressure palsies", "neuropathy, hereditary, with liability to pressure palsies", "NEUROPATHY, HEREDITARY, WITH LIABILITY TO PRESSURE PALSIES", "Neuropathy, Hereditary, With Liability To Pressure Palsies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary neuropathy with liability to pressure palsies", "shortest_name_length": 4}
{"curie": "UMLS:C5555707", "names": ["Metastatic Platinum-Resistant Ovarian Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Platinum-Resistant Ovarian Carcinoma", "shortest_name_length": 47}
{"curie": "MONDO:0008441", "names": ["Spastic Paraplegia With Associated Extrapyramidal Signs", "SPASTIC PARAPLEGIA WITH ASSOCIATED EXTRAPYRAMIDAL SIGNS", "spastic paraplegia with associated extrapyramidal signs"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic paraplegia with associated extrapyramidal signs", "shortest_name_length": 55}
{"curie": "MONDO:0021089", "names": ["Malignant PNS Tumor", "malignant PNS tumor", "Malignant Tumor of PNS", "Malignant PNS Neoplasm", "malignant PNS neoplasm", "malignant tumor of PNS", "Peripheral nerve cancer", "Malignant Neoplasm of PNS", "malignant neoplasm of PNS", "malignant tumor of the PNS", "Cancer of peripheral nerve", "Malignant Tumor of the PNS", "malignant neoplasm of the PNS", "Malignant Neoplasm of the PNS", "malignant peripheral nerve tumor", "Malignant Peripheral Nerve Tumor", "peripheral nervous system cancer", "Malignant Peripheral Nerve Neoplasm", "Malignant tumor of peripheral nerve", "Malignant Tumor of Peripheral Nerve", "malignant peripheral nerve neoplasm", "cancer of peripheral nervous system", "malignant tumor of peripheral nerve", "Malignant tumour of peripheral nerve", "Malignant Neoplasms, Peripheral Nerve", "malignant neoplasms, peripheral nerve", "Peripheral Nerve Neoplasms, Malignant", "Malignant Neoplasm of Peripheral Nerve", "malignant neoplasm of peripheral nerve", "Malignant Tumor of the Peripheral Nerve", "malignant tumor of the peripheral nerve", "malignant neoplasm of peripheral nerves", "Malignant Peripheral Nervous System Tumor", "malignant peripheral nervous system tumor", "Malignant Neoplasm of the Peripheral Nerve", "malignant neoplasm of the peripheral nerve", "Malignant Tumor of Peripheral Nervous System", "Malignant Peripheral Nervous System Neoplasm", "malignant tumor of peripheral nervous system", "malignant peripheral nervous system neoplasm", "Peripheral Nervous System Malignant Neoplasms", "Peripheral Nervous System Neoplasms, Malignant", "Malignant tumor of peripheral nerve (disorder)", "peripheral nervous system neoplasms, malignant", "malignant neoplasm of peripheral nervous system", "Malignant Neoplasm of Peripheral Nervous System", "Malignant Tumor of the Peripheral Nervous System", "malignant tumor of the peripheral nervous system", "malignant neoplasm of the peripheral nervous system", "Malignant Neoplasm of the Peripheral Nervous System", "malignant neoplasm of peripheral nerves (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peripheral nervous system cancer", "shortest_name_length": 19}
{"curie": "UMLS:C1335737", "names": ["Relapsed Hematologic Cancer", "Recurrent Hematologic Cancer", "Relapsed Hematologic Malignancy", "Recurrent Hematologic Malignancy", "Recurrent Hematopoietic and Lymphoid Cell Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Hematologic Malignancy", "shortest_name_length": 27}
{"curie": "MONDO:0020359", "names": ["congenital symblepharon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital symblepharon", "shortest_name_length": 23}
{"curie": "UMLS:C5447598", "names": ["Refractory Rectal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Rectal Squamous Cell Carcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0025667", "names": ["limbal stem cell deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "limbal stem cell deficiency", "shortest_name_length": 27}
{"curie": "MONDO:0008028", "names": ["muscular dystrophy, Barnes type", "Muscular Dystrophy, Barnes Type", "MUSCULAR DYSTROPHY, BARNES TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy, Barnes type", "shortest_name_length": 31}
{"curie": "MONDO:0016213", "names": ["leukonychia totalis-acanthosis-nigricans-like lesions-abnormal hair syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukonychia totalis-acanthosis-nigricans-like lesions-abnormal hair syndrome", "shortest_name_length": 76}
{"curie": "MONDO:0015354", "names": ["HSAN with deafness and global delay", "HSAN with hearing loss and global delay", "hereditary sensory and autonomic neuropathy with deafness and global delay", "Hereditary sensory and autonomic neuropathy with deafness and global delay", "Hereditary sensory and autonomic neuropathy with hearing loss and global delay", "HSAN (hereditary sensory and autonomic neuropathy) with deafness and global delay", "Hereditary sensory and autonomic neuropathy with deafness and global delay (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary sensory and autonomic neuropathy with deafness and global delay", "shortest_name_length": 35}
{"curie": "MONDO:0002714", "names": ["CNS Tumor", "cns tumor", "cns cancer", "cns tumors", "CNS cancer", "CNS Cancer", "cancer cns", "cancers cns", "Neoplasm CNS", "CNS Neoplasm", "CNS neoplasm", "NEOPLASM CNS", "Tumor of CNS", "CNS Neoplasms", "cns neoplasms", "CNS neoplasms", "CNS NEOPLASIA", "Cancer of CNS", "cancer of CNS", "CNS neoplasia", "Neoplasm, CNS", "Neoplasms, CNS", "Neoplasm of CNS", "Tumor of the CNS", "CNS neoplasm NOS", "Cancer of the CNS", "cancer of the CNS", "Neoplasm of the CNS", "Malignant CNS Tumor", "malignant CNS tumor", "malignant tumor of CNS", "malignant CNS neoplasm", "Malignant Tumor of CNS", "Malignant CNS Neoplasm", "CNS Malignant Neoplasms", "Malignant CNS Neoplasms", "CNS malignant neoplasms", "malignant CNS neoplasms", "CNS Neoplasms, Malignant", "CNS neoplasms, malignant", "Malignant Neoplasm of CNS", "malignant neoplasm of CNS", "malignant tumor of the CNS", "Malignant Tumor of the CNS", "central nervous system tumor", "Central Nervous System Tumor", "central nervous system cancer", "central nervous system tumors", "malignant neoplasm of the CNS", "Central Nervous System Cancer", "Central Nervous System Tumors", "Malignant Neoplasm of the CNS", "Tumors, Central Nervous System", "Central nervous system--Tumors", "Neoplasm central nervous system", "central nervous system neoplasm", "Central Nervous System Neoplasm", "Central nervous system neoplasm", "Tumor of Central Nervous System", "cancer of central nervous system", "Central nervous system neoplasia", "Central Nervous System Neoplasms", "Cancer of Central Nervous System", "central nervous system neoplasms", "Neoplasms, Central Nervous System", "Neoplasm of Central Nervous System", "neoplasm of central nervous system", "Neoplasm of central nervous system", "Tumor of the Central Nervous System", "Central nervous system neoplasm NOS", "cancer of the central nervous system", "Tumors of the central nervous system", "Cancer of the Central Nervous System", "Tumours of the central nervous system", "Neoplasm of the Central Nervous System", "Malignant Central Nervous System Tumor", "malignant central nervous system tumor", "Neoplasm of the central nervous system", "Neoplasia of the central nervous system", "Malignant Central Nervous System Neoplasm", "malignant central nervous system neoplasm", "malignant tumor of central nervous system", "Malignant Tumor of Central Nervous System", "Central Nervous System Neoplasms, Malignant", "central nervous system neoplasms, malignant", "malignant neoplasm of central nervous system", "Malignant Neoplasm of Central Nervous System", "Malignant Tumor of the Central Nervous System", "Neoplasm of central nervous system (disorder)", "malignant tumor of the central nervous system", "neoplasm of central nervous system (diagnosis)", "Malignant Neoplasm of the Central Nervous System", "malignant neoplasm of the central nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system cancer", "shortest_name_length": 9}
{"curie": "MONDO:0015590", "names": ["classic paraneoplastic limbic encephalitis", "classic paraneoplastic limbic encephalitis, with or without intracellular antigens"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "classic paraneoplastic limbic encephalitis", "shortest_name_length": 42}
{"curie": "MONDO:0012966", "names": ["MVCD4", "NEPHROPATHY, DIABETIC, SUSCEPTIBILITY TO", "nephropathy, diabetic, susceptibility to", "microvascular complications of diabetes 4", "IL1RN microvascular complications of diabetes, susceptibility", "MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 4", "microvascular complications of diabetes, susceptibility to, 4", "microvascular complications of diabetes, susceptibility to, type 4", "MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 4 (finding)", "microvascular complications of diabetes, susceptibility caused by mutation in IL1RN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microvascular complications of diabetes, susceptibility to, 4", "shortest_name_length": 5}
{"curie": "UMLS:C4053795", "names": ["Non-Functioning PitNET/Microadenoma", "Nonfunctional Pituitary Microadenoma", "Nonfunctional Pituitary Gland Microadenoma", "Nonfunctioning Pituitary Gland Microadenoma", "Non-Functioning Pituitary Gland Microadenoma", "Non-Functioning Pituitary Neuroendocrine Tumor/Microadenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Functioning Pituitary Neuroendocrine Tumor/Microadenoma", "shortest_name_length": 35}
{"curie": "UMLS:C4330998", "names": ["Perinatal-Stress Induced Hyperinsulinism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perinatal-Stress Induced Hyperinsulinism", "shortest_name_length": 40}
{"curie": "UMLS:C1334687", "names": ["Megakaryocytic Tumor", "Megakaryocytic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Megakaryocytic Neoplasm", "shortest_name_length": 20}
{"curie": "UMLS:C4087338", "names": ["Mite allergy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mite allergy", "shortest_name_length": 12}
{"curie": "MONDO:0016342", "names": ["familial isolated ARVD", "Familial isolated ARVC", "Familial isolated ARVD", "familial isolated ARVC", "Familial isolated arrhythmogenic ventricular dysplasia", "familial isolated arrhythmogenic ventricular dysplasia", "familial isolated arrhythmogenic ventricular cardiomyopathy", "Familial isolated arrhythmogenic ventricular cardiomyopathy", "familial isolated arrhythmogenic right ventricular dysplasia", "Familial isolated arrhythmogenic right ventricular dysplasia", "familial isolated arrhythmogenic right ventricular cardiomyopathy", "Familial isolated arrhythmogenic right ventricular cardiomyopathy", "Familial isolated ARVD (arrhythmogenic right ventricular dysplasia)", "Familial isolated arrhythmogenic right ventricular dysplasia (disorder)", "familial isolated arrhythmogenic right ventricular dysplasia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial isolated arrhythmogenic right ventricular dysplasia", "shortest_name_length": 22}
{"curie": "UMLS:C1709028", "names": ["Microscopic Thymoma", "Nodular Hyperplasia of the Thymic Epithelium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Microscopic Thymoma", "shortest_name_length": 19}
{"curie": "UMLS:C0865214", "names": ["autosomal recessive agammaglobulinemia", "Autosomal recessive agammaglobulinemia", "Autosomal Recessive Agammaglobulinemia", "agammaglobulinemia; autosomal recessive", "autosomal recessive; agammaglobulinemia", "autosomal recessive agammaglobulinemia (diagnosis)", "Autosomal Recessive Agammaglobulinemia (AR Agammaglobulinemia)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive agammaglobulinemia", "shortest_name_length": 38}
{"curie": "MONDO:0011169", "names": ["KLICK", "KLICK Syndrome", "KLICK syndrome", "Klick syndrome", "KLICK SYNDROME", "Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma", "Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome", "keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome", "KERATOSIS LINEARIS WITH ICHTHYOSIS CONGENITA AND SCLEROSING KERATODERMA", "keratosis linearis with ichthyosis congenita and sclerosing keratoderma", "Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome", "Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C1336481", "names": ["Skin Cancer Stage I", "Stage I Skin Cancer", "Skin Carcinoma Stage I", "Carcinoma of Skin Stage I", "Stage I Skin Cancer AJCC v7", "Carcinoma of the Skin Stage I", "stage I nonmelanoma skin cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Skin Cancer", "shortest_name_length": 19}
{"curie": "MONDO:0013436", "names": ["RP39", "RETINITIS PIGMENTOSA 39", "retinitis pigmentosa 39", "USH2A retinitis pigmentosa", "retinitis pigmentosa type 39", "RETINITIS PIGMENTOSA 39 (disorder)", "retinitis pigmentosa caused by mutation in USH2A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 39", "shortest_name_length": 4}
{"curie": "MONDO:0017939", "names": ["classic MmD", "minicore myopathy", "classic multiminicore disease", "classic multiminicore myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "minicore myopathy", "shortest_name_length": 11}
{"curie": "UMLS:C5420860", "names": ["Unresectable Poorly Differentiated Thyroid Gland Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Poorly Differentiated Thyroid Gland Carcinoma", "shortest_name_length": 58}
{"curie": "MONDO:0007492", "names": ["Dyt1", "EOTD", "DYT1", "DYT-TOR1A", "dystonia 1", "Schwalbe disease", "Torsion dystonia", "torsion dystonia", "Torsion Dystonia", "torsion; dystonia", "dystonia; torsion", "Oppenheim Dystonia", "Oppenheim dystonia", "Dystonias, Torsion", "torsion dystonia 1", "DYT-TOR1A dystonia", "dystonia-1, torsion", "idiopathic dystonia", "Oppenheim's Dystonia", "Oppenheim's dystonia", "torsion dystonia type 1", "genetic torsion dystonia", "idiopathic dystonia DYT1", "Ziehen Oppenheim disease", "Primary Torsion Dystonia", "dystonia genetic torsion", "Genetic torsion dystonia", "Oppenheim Ziehen Disease", "Ziehen-Oppenheim disease", "Primary torsion dystonia", "Oppenheim-Ziehen Disease", "Schwalbe-Ziehen-Oppenheim", "Childhood Torsion Disease", "Progressive Torsion Spasm", "Torsion Disease, Childhood", "Spasm, Progressive Torsion", "Torsion Spasm, Progressive", "Idiopathic torsion dystonia", "Idiopathic Torsion Dystonia", "Torsion dystonia (disorder)", "idiopathic torsion dystonia", "Early-Onset Primary Dystonia", "EARLY-ONSET TORSION DYSTONIA", "Early Onset Torsion Dystonia", "Early-onset Primary dystonia", "early onset torsion dystonia", "early-onset torsion dystonia", "Idiopathic Torsion Dystonias", "Early-Onset Torsion Dystonia", "Torsion dystonia, idiopathic", "early-onset primary dystonia", "primary dystonia early-onset", "Torsion Disease of Childhood", "early onset primary dystonia", "Early-onset torsion dystonia", "Bilateral paraspasm syndrome", "Dystonia, Idiopathic Torsion", "Early onset primary dystonia", "Torsion Dystonia, Idiopathic", "Early-onset primary dystonia", "Early Onset Primary Dystonia", "Early onset torsion dystonia", "Dystonia Musculorum Deformans", "Dystonia musculorum deformans", "Dystonia Deformans Musculorum", "Early-onset isolated dystonia", "Dystonias, Idiopathic Torsion", "dystonia musculorum deformans", "Dystonia Deformans Progressiva", "dystonia deformans progressiva", "Dystonia deformans progressiva", "DYSTONIA DEFORMANS PROGRESSIVA", "Dystonia lenticularis syndrome", "Dystonia, musculorum deformans", "dystonia; musculorum deformans", "dystonia; deformans progressive", "dystonia musculorum deformans 1", "musculorum; dystonia, deformans", "Dystonia, deformans progressiva", "deformans progressive; dystonia", "DYSTONIA MUSCULORUM DEFORMANS 1", "Dystonia Musculorum Deformans 1", "Schwalbe-Ziehen-Oppenheim disease", "Idiopathic (torsion) dystonia NOS", "Torsion dystonia fragment syndrome", "(Schwalbe-) Ziehen-Oppenheim disease", "Dystonia musculorum deformans type 1", "genetic torsion dystonia (diagnosis)", "Autosomal Dominant Torsion Dystonia 1", "torsion dystonia 1, autosomal dominant", "Idiopathic torsion dystonia (disorder)", "Torsion dystonia 1, autosomal dominant", "Dystonia 1, Torsion, Autosomal Dominant", "dystonia 1, torsion, Autosomal dominant", "DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT", "dystonia 1, torsion, autosomal dominant", "idiopathic dystonia musculorum deformans", "early-onset generalized torsion dystonia", "Early-Onset Generalized Torsion Dystonia", "Early-onset generalized torsion dystonia", "primary dystonia early-onset (diagnosis)", "dystonia musculorum deformans (diagnosis)", "Early-onset generalized limb-onset dystonia", "early-onset generalized limb-onset dystonia", "Schwalbe-Ziehen-Oppenheim disease (diagnosis)", "idiopathic dystonia musculorum deformans (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early-onset generalized limb-onset dystonia", "shortest_name_length": 4}
{"curie": "OMIM:616089", "names": [], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"]}
{"curie": "UMLS:C0278849", "names": ["stage I papillary thyroid cancer", "Stage I Papillary Thyroid Cancer", "thyroid cancer, stage I papillary", "papillary thyroid cancer, stage I", "Stage I Thyroid Papillary Carcinoma", "Stage I Thyroid Gland Papillary Cancer", "Stage I Papillary Carcinoma of Thyroid", "Stage I Papillary Thyroid Gland Carcinoma", "Stage I Thyroid Gland Papillary Carcinoma", "Stage I Papillary Carcinoma of the Thyroid", "adenocarcinoma, papillary, thyroid, stage I", "mixed adenocarcinoma of the thyroid, stage I", "Stage I Papillary Carcinoma of Thyroid Gland", "Stage I Papillary Carcinoma of the Thyroid Gland", "papillary adenocarcinoma of the thyroid, stage I", "Stage I Thyroid Gland Papillary Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Thyroid Gland Papillary Carcinoma AJCC v7", "shortest_name_length": 32}
{"curie": "UMLS:C0401013", "names": ["Fungal peritonitis", "fungal peritonitis", "Fungal peritonitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fungal peritonitis", "shortest_name_length": 18}
{"curie": "UMLS:C0220656", "names": ["ASCITES MALIGNANT", "Malignant Ascites", "Malignant ascites", "malignant ascites", "MALIGNANT ASCITES", "ascites, malignant", "Ascites, Malignant", "malignant; ascites", "ascites; malignant", "Malignant ascites, NOS", "Malignant ascites (disorder)", "malignant peritoneal effusion", "malignant ascites (diagnosis)", "Malignant peritoneal effusion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant ascites", "shortest_name_length": 17}
{"curie": "MONDO:0015178", "names": ["congenital intestinal transport defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital intestinal transport defect", "shortest_name_length": 38}
{"curie": "OMIM:617234", "names": ["PREMBL2", "PREIMPLANTATION EMBRYONIC LETHALITY 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 7}
{"curie": "MONDO:0019141", "names": ["POROK1", "porokeratosis", "Mibelli's disease", "porokeratosis mibelli", "Mibelli Porokeratosis", "Porokeratosis, Mibelli", "porokeratosis of Mibelli", "POROKERATOSIS OF MIBELLI", "Porokeratosis of Mibelli", "porokeratosis of mibelli", "POROKERATOSIS 1, MULTIPLE TYPES", "Porokeratosis of Mibelli (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "porokeratosis of Mibelli", "shortest_name_length": 6}
{"curie": "MONDO:0036779", "names": ["axilla tumor", "axilla neoplasm", "tumor of axilla", "Axillary Neoplasm", "axillary neoplasm", "neoplasm of axilla", "Neoplasm of axilla", "Neoplasm of axilla (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "axillary neoplasm", "shortest_name_length": 12}
{"curie": "MONDO:0011870", "names": ["AEI", "AEI1", "Ciehk", "CIEHK1", "annular epidermolytic ichthyosis", "Annular epidermolytic ichthyosis", "epidermolytic ichthyosis, annular", "Epidermolytic Ichthyosis, Annular", "ichthyosis, annular epidermolytic", "ICHTHYOSIS, ANNULAR EPIDERMOLYTIC, 1", "Annular epidermolytic ichthyosis (disorder)", "ichthyosis, cyclic, with epidermolytic hyperkeratosis", "ICHTHYOSIS, CYCLIC, WITH EPIDERMOLYTIC HYPERKERATOSIS", "Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "annular epidermolytic ichthyosis", "shortest_name_length": 3}
{"curie": "MONDO:0008584", "names": ["torus palatinus and torus mandibularis", "TORUS PALATINUS AND TORUS MANDIBULARIS", "Torus Palatinus and Torus Mandibularis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "torus palatinus and torus mandibularis", "shortest_name_length": 38}
{"curie": "UMLS:C1512695", "names": ["Increased NFkappaB Pathway Activation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Increased NFkappaB Pathway Activation", "shortest_name_length": 37}
{"curie": "MONDO:0010015", "names": ["ASGD7", "COPOA", "CCMCO", "anterior segment dysgenesis", "ANTERIOR SEGMENT DYSGENESIS 7", "anterior segment dysgenesis 7", "PXDN anterior segment dysgenesis", "anterior segment developmental anomaly", "sclerocornea with other ocular anomalies", "SCLEROCORNEA WITH OTHER OCULAR ANOMALIES", "sclerocornea with Other ocular anomalies", "corneal opacification and other ocular anomalies", "anterior segment dysgenesis 7, with sclerocornea", "corneal opacification with other ocular anomalies", "CORNEAL OPACIFICATION WITH OTHER OCULAR ANOMALIES", "corneal opacification with Other ocular anomalies", "congenital cataract microcornea with corneal opacity", "Congenital cataract microcornea with corneal opacity", "anterior segment dysgenesis caused by mutation in PXDN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anterior segment dysgenesis 7", "shortest_name_length": 5}
{"curie": "MONDO:0044972", "names": ["eosinophil disorder", "disease of eosinophil", "Disorder of eosinophil", "disorder of eosinophil", "eosinophil disease or disorder", "disease or disorder of eosinophil", "Disorder of eosinophil (disorder)", "disorder of eosinophil (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eosinophil disorder", "shortest_name_length": 19}
{"curie": "UMLS:C2938917", "names": ["cerebellar mutism", "Cerebellar mutism", "Cerebellar Mutism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebellar mutism", "shortest_name_length": 17}
{"curie": "UMLS:C5419163", "names": ["COVID-19-Associated Pneumonia", "SARS-CoV-2 -Associated Pneumonia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "COVID-19-Associated Pneumonia", "shortest_name_length": 29}
{"curie": "MONDO:0008813", "names": ["Arachnoid Cyst", "ARACHNOID CYST", "cyst arachnoid", "Arachnoid cyst", "arachnoid cyst", "arachnoid; cyst", "Arachnoid cysts", "Arachnoid Cysts", "cyst; arachnoid", "arachnoid cysts", "Cyst, Arachnoid", "Cysts, Arachnoid", "Arachnoidal cyst", "Leptomeningeal Cyst", "leptomeningeal cyst", "Cyst, Leptomeningeal", "Leptomeningeal Cysts", "Cysts, Leptomeningeal", "Arachnoid Diverticula", "Diverticula, Arachnoid", "Arachnoid Diverticulas", "Diverticulas, Arachnoid", "Arachnoid cyst (disorder)", "arachnoid cyst (diagnosis)", "Arachnoid cyst (morphologic abnormality)", "Fluid-filled sac located in membrane surrounding brain or spinal cord"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arachnoid cyst", "shortest_name_length": 14}
{"curie": "UMLS:C1608954", "names": ["Infusion Site Extravasation", "Infusion site extravasation", "infusion site extravasation", "infusion site extravasation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infusion Site Extravasation", "shortest_name_length": 27}
{"curie": "MONDO:0001082", "names": ["cancer lymph node", "Lymph Node Cancer", "lymph node cancer", "cancer lymph nodes", "cancers lymph node", "Lymph Node Neoplasm", "lymph node neoplasm", "cancer of lymph node", "Cancer of lymph node", "neoplasm of lymph node", "Neoplasm of lymph node", "malignant lymph node neoplasm", "malignant tumor of lymph node", "Malignant Lymph Node Neoplasm", "malignant neoplasm of lymph node", "Neoplasm of lymph node (disorder)", "neoplasm of lymph node (diagnosis)", "malignant neoplasm of lymph node (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymph node cancer", "shortest_name_length": 17}
{"curie": "UMLS:C5206573", "names": ["Metastatic Thymic Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Thymic Neuroendocrine Neoplasm", "shortest_name_length": 41}
{"curie": "MONDO:0007238", "names": ["BNAH1", "amazia", "athelia", "Athelia", "Amastia", "amastia", "Absent nipple", "absent nipple", "nipple; absent", "Absent nipples", "absent nipples", "agenesis; nipple", "nipple; agenesis", "breast nipple absent", "Absent nipple (finding)", "Congenital absent nipple", "absent breasts and nipples", "complete absence of breasts", "congenital absence of nipple", "Congenital absence of nipple", "absent nipple (physical finding)", "[OBSOLETE] Absent breasts and nipples", "Congenital absence of nipple (disorder)", "congenital absence of nipple (diagnosis)", "breasts and/or nipples, aplasia or hypoplasia of, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amastia", "shortest_name_length": 5}
{"curie": "MONDO:0033656", "names": ["MC4DN21", "mitochondrial complex 4 deficiency, nuclear type 21", "MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 21", "mitochondrial complex IV deficiency, nuclear type 21"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 4 deficiency, nuclear type 21", "shortest_name_length": 7}
{"curie": "MONDO:0700008", "names": ["chromosome 1 disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 1 disorder", "shortest_name_length": 21}
{"curie": "MONDO:0021699", "names": ["Alcohol-Induced Disorder", "Alcohol induced disorder", "alcohol-induced disorder", "Alcohol Induced Disorders", "Alcohol-Induced Disorders", "alcohol-induced disorders", "alcohol induced disorders", "Disorder caused by alcohol", "Disorder caused by alcohol (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alcohol-induced disorders", "shortest_name_length": 24}
{"curie": "UMLS:C4526969", "names": ["Stage III Gastric and Omental GIST AJCC v8", "Stage III Gastric and Omental Gastrointestinal Stromal Tumor AJCC v8", "Stage III Gastric (Stomach) and Omental Gastrointestinal Stromal Tumor (GIST)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Gastric and Omental Gastrointestinal Stromal Tumor AJCC v8", "shortest_name_length": 42}
{"curie": "MONDO:0017404", "names": ["distal dup(X)q(28)", "distal trisomy Xq28", "Xq28 Microduplication", "distal Xq28 microduplication syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal Xq28 microduplication syndrome", "shortest_name_length": 18}
{"curie": "UMLS:C5206812", "names": ["ASPH-Positive Head and Neck Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ASPH-Positive Head and Neck Squamous Cell Carcinoma", "shortest_name_length": 51}
{"curie": "MONDO:0020712", "names": ["SRXY1", "TDFX, FORMERLY", "SRVX, FORMERLY", "46,XY Sex Reversal 1", "46,XY SEX REVERSAL 1", "46,XY sex reversal 1", "46,XY sex reversal type 1", "46XY sex reversal 1, Y-linked", "46,XY sex reversal, SRY-related", "46,XY SEX REVERSAL, SRY-RELATED", "Gonadal Dysgenesis, Xy Female Type", "SEX-REVERSING LOCUS ON X, FORMERLY", "46,XY true hermaphroditism, SRY-related", "46,XY TRUE HERMAPHRODITISM, SRY-RELATED", "46,Xy True Hermaphroditism, Sry-Related", "46,XY gonadal dysgenesis, complete, SRY-related", "46,Xy Gonadal Dysgenesis, Complete, Sry-Related", "46,XY GONADAL DYSGENESIS, COMPLETE, SRY-RELATED", "TESTIS-DETERMINING FACTOR, X-CHROMOSOMAL, FORMERLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XY sex reversal 1", "shortest_name_length": 5}
{"curie": "MONDO:0012556", "names": ["CDG1m", "CDGIm", "CDG1M", "CDG-Im", "CDG Im", "DK1-CDG", "DK1 DEFICIENCY", "Dk1 deficiency", "DOLK-CDG (CDG-Im)", "CDG syndrome type Im", "Dolichol kinase deficiency", "dolichol kinase deficiency", "DOLICHOL KINASE DEFICIENCY", "Dolichol Kinase Deficiency", "congenital disorder of glycosylation 1m", "congenital disorder of glycosylation Im", "DK1-congenital disorder of glycosylation", "DOLK-congenital disorder of glycosylation", "congenital disorder of glycosylation type Im", "congenital disorder of glycosylation type 1m", "Congenital disorder of glycosylation type 1m", "Congenital disorder of glycosylation type Im", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Im", "Congenital Disorder Of Glycosylation, Type Im", "congenital disorder of glycosylation, type Im", "Carbohydrate deficient glycoprotein syndrome type 1m", "carbohydrate deficient glycoprotein syndrome type Im", "Carbohydrate deficient glycoprotein syndrome type Im", "CDG1M - carbohydrate deficient glycoprotein syndrome type 1m", "Hypotonia and ichthyosis due to dolichol phosphate deficiency", "hypotonia and ichthyosis due to dolichol phosphate deficiency", "Carbohydrate deficient glycoprotein syndrome type 1m (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DK1-congenital disorder of glycosylation", "shortest_name_length": 5}
{"curie": "MONDO:0036870", "names": ["lymph vessel tumor", "Lymph Vessel Tumor", "Lymph Vessel Neoplasm", "lymph vessel neoplasm", "Tumor of Lymph Vessel", "tumor of lymph vessel", "Lymphatic vessel tumor", "Lymphatic Vessel Tumor", "lymphatic vessel tumor", "Lymphatic vessel tumour", "Tumor, Lymphatic Vessel", "Lymphatic Vessel Tumors", "LYMPHATIC VESSEL TUMORS", "neoplasm of lymph vessel", "Tumors, Lymphatic Vessel", "Neoplasm of Lymph Vessel", "Lymphatic vessel neoplasm", "Tumor of the Lymph Vessel", "Tumor of Lymphatic Vessel", "lymphatic vessel neoplasm", "tumor of lymphatic vessel", "tumor of the lymph vessel", "Lymphatic Vessel Neoplasm", "Neoplasm of Lymphatic Vessel", "Neoplasm of the Lymph Vessel", "neoplasm of the lymph vessel", "neoplasm of lymphatic vessel", "Tumor of the Lymphatic Vessel", "tumor of the lymphatic vessel", "neoplasm of the lymphatic vessel", "Neoplasm of the Lymphatic Vessel", "Lymphatic vessel tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphatic vessel neoplasm", "shortest_name_length": 18}
{"curie": "UMLS:C1828221", "names": ["Non Dystrophic Myotonia", "Non-Dystrophic Myotonia", "Non dystrophic myotonia", "Non dystrophic myotonia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non dystrophic myotonia", "shortest_name_length": 23}
{"curie": "MONDO:0023561", "names": ["Koone Rizzo Elias syndrome", "Koone-Rizzo-Elias syndrome", "Ichthyosis, mental retardation and asymptomatic spasticity", "ichthyosis, mental retardation and asymptomatic spasticity", "ichthyosis, intellectual disability and asymptomatic spasticity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Koone-Rizzo-Elias syndrome", "shortest_name_length": 26}
{"curie": "MONDO:0001998", "names": ["Foster Kennedy Syndrome", "syndrome foster-kennedy", "Foster-Kennedy Syndrome", "foster-kennedy syndrome", "Foster Kennedy syndrome", "foster kennedy syndrome", "Foster-Kennedy syndrome", "Syndrome, Foster-Kennedy", "Foster Kennedy's syndrome", "Foster-Kennedy syndrome (disorder)", "Foster Kennedy syndrome (diagnosis)", "papilledema with optic atrophy in contralateral eye", "papilledema with optic atrophy in contralateral eye (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Foster-Kennedy syndrome", "shortest_name_length": 23}
{"curie": "UMLS:C1562543", "names": ["Ocular histoplasmosis syndrome", "OHS-ocular histoplasmosis syndrome", "Ocular histoplasmosis syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ocular histoplasmosis syndrome", "shortest_name_length": 30}
{"curie": "MONDO:0009087", "names": ["deafness, neural, congenital moderate", "DEAFNESS, NEURAL, CONGENITAL MODERATE", "Deafness, Neural, Congenital Moderate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness, neural, congenital moderate", "shortest_name_length": 37}
{"curie": "MONDO:0007599", "names": ["MCFD6", "FMFD VI", "multiple coagulation Factor deficiency 6", "Multiple Coagulation Factor Deficiency VI", "MULTIPLE COAGULATION FACTOR DEFICIENCY VI", "Factor IX and Factor XI, Combined Deficiency", "factor 9 and Factor XI, combined deficiency of", "FACTOR IX AND FACTOR XI, COMBINED DEFICIENCY OF", "factor IX and factor XI, combined deficiency OF", "familial multiple coagulation Factor deficiency 6", "Familial Multiple Coagulation Factor Deficiency VI", "FAMILIAL MULTIPLE COAGULATION FACTOR DEFICIENCY VI"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "factor 9 and Factor XI, combined deficiency of", "shortest_name_length": 5}
{"curie": "UMLS:C0016545", "names": ["Foreign body muscle granuloma", "foreign body granuloma of muscle", "Foreign Body Granuloma of Muscle", "Foreign body granuloma of muscle", "Foreign body granuloma of muscle (disorder)", "foreign body granuloma of muscle (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Foreign body granuloma of muscle", "shortest_name_length": 29}
{"curie": "MONDO:0001224", "names": ["Angelucci syndrome", "Angelucci's syndrome", "Acute atopic conjunctivitis", "conjunctivitis acute atopic", "acute atopic conjunctivitis", "Acute Atopic Conjunctivitis", "CONJUNCTIVITIS, ANAPHYLACTIC", "Acute allergic conjunctivitis", "Acute atopic conjunctivitis (disorder)", "acute atopic conjunctivitis (diagnosis)", "Critical allergic conjunctivitis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Angelucci syndrome", "shortest_name_length": 18}
{"curie": "MONDO:0003880", "names": ["Ceruminous carcinoma", "ceruminous carcinoma", "ceruminous; carcinoma", "carcinoma; ceruminous", "ceruminous adenocarcinoma", "Ceruminous adenocarcinoma", "Ceruminous Adenocarcinoma", "ceruminous; adenocarcinoma", "adenocarcinoma; ceruminous", "CARCINOMA, CERUMINOUS GLAND, MALIGNANT", "carcinoma, ceruminous gland, malignant", "ceruminous adenocarcinoma (morphologic abnormality)", "Ceruminous adenocarcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ceruminous carcinoma", "shortest_name_length": 20}
{"curie": "UMLS:C2984082", "names": ["Uterine Corpus Cancer by AJCC v7 Stage", "Uterine Corpus Carcinoma or Carcinosarcoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Corpus Cancer by AJCC v7 Stage", "shortest_name_length": 38}
{"curie": "MONDO:0016708", "names": ["embryonal tumor of neuroepithelial tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "embryonal tumor of neuroepithelial tissue", "shortest_name_length": 41}
{"curie": "MONDO:0013380", "names": ["LPRD3", "LEOPARD syndrome 3", "leopard syndrome 3", "LEOPARD SYNDROME 3", "Leopard syndrome type 3", "Noonan syndrome with multiple lentigines 3", "BRAF Noonan syndrome with multiple lentigines", "Noonan syndrome with multiple lentigines caused by mutation in BRAF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "LEOPARD syndrome 3", "shortest_name_length": 5}
{"curie": "UMLS:C3272257", "names": ["Severe Cardiac Valve Regurgitation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Severe Cardiac Valve Regurgitation", "shortest_name_length": 34}
{"curie": "UMLS:C0474796", "names": ["Tumor Morphology", "Tumor_Morphology", "Tumor morphology", "Tumour morphology", "Neoplasm by Morphology", "Morphology of neoplasms"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplasm by Morphology", "shortest_name_length": 16}
{"curie": "MONDO:0014343", "names": ["DBQD2", "Desbuquois dysplasia 2", "DESBUQUOIS DYSPLASIA 2", "Baratela-Scott syndrome", "BARATELA-SCOTT SYNDROME", "XYLT1 Desbuquois dysplasia", "Desbuquois dysplasia type 2", "Desbuquois dysplasia caused by mutation in XYLT1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Desbuquois dysplasia 2", "shortest_name_length": 5}
{"curie": "UMLS:C5417704", "names": ["AVPCa", "Anaplastic Prostate Cancer", "Anaplastic Prostate Carcinoma", "Aggressive Variant Prostate Cancer", "Aggressive Variant Prostate Carcinoma", "Treatment-Related Anaplastic Prostate Cancer", "Metastatic Aggressive Variant Prostate Cancer", "Treatment-Related Anaplastic Prostate Carcinoma", "Treatment-Related Neuroendocrine Prostate Cancer", "Metastatic Aggressive Variant Prostate Carcinoma", "Treatment-Related Neuroendocrine Prostate Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aggressive Variant Prostate Carcinoma", "shortest_name_length": 5}
{"curie": "MONDO:0100352", "names": ["PKD", "PKC", "EKD1", "DYT10", "DYT-PRRT2", "PxMD-PRRT2", "dystonia 10", "DYSTONIA 10", "Dystonia 10", "PKD Dystonia", "Familial PKD", "Familial paroxysmal dystonia", "Dystonia, familial paroxysmal", "dystonia, familial paroxysmal", "DYSTONIA, FAMILIAL PAROXYSMAL", "EPISODIC KINESIGENIC DYSKINESIA 1", "episodic kinesigenic dyskinesia 1", "PAROXYSMAL KINESIGENIC DYSKINESIA", "paroxysmal kinesigenic dyskinesia", "Episodic Kinesigenic Dyskinesia 1", "Episodic Kinesigenic Dyskinesia-1", "Paroxysmal Kinesigenic Dyskinesia", "Paroxysmal kinesigenic dyskinesia", "Paroxysmal kinesigenic choreathetosis", "PRRT2 episodic kinesigenic dyskinesia", "Paroxysmal kinesigenic choreoathetosis", "paroxysmal kinesigenic choreoathetosis", "PAROXYSMAL KINESIGENIC CHOREOATHETOSIS", "episodic kinesigenic dyskinesia type 1", "Familial Paroxysmal Kinesigenic Dyskinesia", "Familial paroxysmal kinesigenic dyskinesia", "Paroxysmal kinesigenic dyskinesia (disorder)", "paroxysmal kinesigenic dyskinesia (diagnosis)", "episodic kinesigenic dyskinesia caused by mutation in PRRT2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "episodic kinesigenic dyskinesia 1", "shortest_name_length": 3}
{"curie": "MONDO:0040671", "names": ["favism", "G6PD deficiency", "G6PD class V variant anemia", "G-6-PD class V variant anemia", "G-6-PD class V variant anaemia", "class V glucose-6-phosphate dehydrogenase deficiency", "Glucose-6-phosphate dehydrogenase deficiency class V variant anemia", "glucose-6-phosphate dehydrogenase deficiency class V variant anemia", "Glucose-6-phosphate dehydrogenase deficiency class V variant anaemia", "Glucose-6-phosphate dehydrogenase deficiency class V variant anemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "class V glucose-6-phosphate dehydrogenase deficiency", "shortest_name_length": 6}
{"curie": "MONDO:0054737", "names": ["FRASRS1", "Fraser syndrome", "FRASER SYNDROME 1", "Fraser syndrome 1", "cryptophthalmos-syndactyly syndrome", "cryptophthalmos with Other malformations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fraser syndrome 1", "shortest_name_length": 7}
{"curie": "MONDO:0015389", "names": ["Extra nostril", "Accessory nares", "accessory nostril", "Accessory nostril", "Supernumerary naris", "Supernumerary nares", "supernumerary naris", "Supernumerary nostril", "supernumerary nostril", "Supernumerary nostrils", "Accessory anterior naris", "Accessory anterior naris (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "supernumerary nostril", "shortest_name_length": 13}
{"curie": "MONDO:0021378", "names": ["Endocardial Tumor", "endocardium tumor", "endocardial tumor", "endocardium neoplasm", "tumor of endocardium", "endocardial neoplasm", "Endocardial Neoplasm", "Tumor of Endocardium", "Neoplasm of Endocardium", "neoplasm of endocardium", "Neoplasm of endocardium", "Tumor of the Endocardium", "tumor of the endocardium", "neoplasm of the endocardium", "Neoplasm of the Endocardium", "endocardium neoplasm (disease)", "Neoplasm of endocardium (disorder)", "neoplasm of endocardium (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplasm of endocardium", "shortest_name_length": 17}
{"curie": "MONDO:8000010", "names": ["APLS", "Classic APLS", "Hughes syndrome", "Hughes Syndrome", "Syndrome, Hughes", "anticardiolipin syndrome", "Anticardiolipin syndrome", "Antiphospholipid syndrome", "Antiphospholipid Syndrome", "antiphospholipid syndrome", "syndrome; anticardiolipin", "anticardiolipin; syndrome", "antiphospholipid; syndrome", "Syndrome, Antiphospholipid", "anti-phospholipid syndrome", "syndrome; antiphospholipid", "anti phospholipid syndrome", "Anti-Phospholipid Syndrome", "Anti Phospholipid Syndrome", "antiphospholipids syndrome", "anti phospholipids syndrome", "Syndrome, Anti-Phospholipid", "familial lupus anticoagulant", "lupus anticoagulant, familial", "APS - Antiphospholipid syndrome", "APL - Antiphospholipid syndrome", "Classic antiphospholipid syndrome", "Antiphospholipid antibody syndrome", "Antiphospholipid Antibody Syndrome", "antiphospholipid antibody syndrome", "Antibody Syndrome, Antiphospholipid", "Anti Phospholipid Antibody Syndrome", "Antiphospholipid Antibody Syndromes", "Anti-Phospholipid Antibody Syndrome", "Syndrome, Antiphospholipid Antibody", "Syndrome, Anti-Phospholipid Antibody", "Antiphospholipid syndrome (disorder)", "Antibody Syndrome, Anti-Phospholipid", "antiphospholipid syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "antiphospholipid syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0266449", "names": ["brain; anomaly", "anomaly; brain", "brain deformity", "deformity; brain", "brain; deformity", "brain deformities", "Deformity of brain", "Brain malformation", "brain malformation", "malformation brain", "BRAIN MALFORMATION", "Brain malformations", "brain malformations", "Brain Malformations", "Deformity of brain, NOS", "Congenital brain anomaly", "congenital brain disorder", "brain; disease, congenital", "Congenital disease of brain", "Congenital anomaly of brain", "Congenital brain anomaly NOS", "Congenital deformity of brain", "Cerebral disorders congenital", "Congenital anomaly NOS of brain", "Non-syndromic brain malformation", "Congenital anomaly of brain, NOS", "Congenital disease of brain, NOS", "CONGENITAL ANOMALIES OF THE BRAIN", "Congenital deformity NOS of brain", "Non-syndromic cerebral malformation", "Congenital anomaly of brain (disorder)", "disease (or disorder); brain, congenital", "Congenital malformation of brain, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital anomaly of brain", "shortest_name_length": 14}
{"curie": "UMLS:C0751293", "names": ["Semantic Memory Disorder", "Semantic Memory Disorders", "Memory Disorder, Semantic", "Memory Disorders, Semantic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Memory Disorder, Semantic", "shortest_name_length": 24}
{"curie": "MONDO:0018046", "names": ["Braddock Carey syndrome", "thrombocytopenia Robin sequence", "Thrombocytopenia Robin sequence", "thrombocytopenia-robin sequence syndrome", "congenital thrombocytopenia, Robin sequence, agenesis of the corpus callosum, distinctive facies and developmental delay"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombocytopenia-robin sequence syndrome", "shortest_name_length": 23}
{"curie": "UMLS:C0277334", "names": ["Moniliformiosis", "Infection by Moniliformis", "Infection by Moniliformis, NOS", "Infection caused by Moniliformis", "Infection caused by Moniliformis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infection by Moniliformis", "shortest_name_length": 15}
{"curie": "UMLS:C4727284", "names": ["Locally Advanced Unresectable Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Unresectable Sarcoma", "shortest_name_length": 37}
{"curie": "UMLS:C5420044", "names": ["Sinonasal Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Sarcoma", "shortest_name_length": 17}
{"curie": "UMLS:C5669822", "names": ["Refractory Vaginal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Vaginal Squamous Cell Carcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0005154", "names": ["hepatopathy", "Hepatopathy", "Disease;liver", "LIVER DISEASE", "liver disease", "Liver Disease", "Liver disease", "liver diseases", "liver abnormal", "abnormal liver", "Liver disorder", "LIVER DISORDER", "Disorder liver", "liver; disease", "Liver diseases", "Disease, Liver", "liver disorder", "Liver Disorder", "DISORDER LIVER", "Liver Diseases", "LIVER ABNORMAL", "Abnormal liver", "HEPATIC DISEASE", "Diseases, Liver", "liver disorders", "Liver--Diseases", "disorder; liver", "hepatic disease", "Liver Disorders", "Hepatic disease", "Hepatic Diseases", "DISORDER HEPATIC", "FECTOR HEPATICUS", "Disease of liver", "disease of liver", "fector hepaticus", "Disorder hepatic", "Hepatic Disorder", "hepatic disorder", "Liver abnormality", "disorder of liver", "Hepatic Disorders", "diseases of liver", "Disorder of liver", "Diseases of liver", "Liver disease nos", "liver diseases of", "hepatic disorders", "LD - Liver disease", "Liver disease, NOS", "Hepatic disease NOS", "Hepatic disorder NOS", "HEPATIC DISEASE (NOS)", "diseases of the liver", "DISEASES OF THE LIVER", "Disease of liver, NOS", "HEPATIC DISORDER (NOS)", "HEPATOCELLULAR DISEASE", "Disease hepatocellular", "DISEASE HEPATOCELLULAR", "hepatocellular disease", "HEPATIC: HEPATOCELLULAR", "Abnormality of the liver", "liver disease or disorder", "Liver disease, unspecified", "Diseases of liver (K70-K77)", "disease or disorder of liver", "Disorder of liver (disorder)", "Unspecified disorder of liver", "hepatic disorders (diagnosis)", "Liver and Intrahepatic Bile Duct Disorder", "liver and intrahepatic bile duct disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "liver disorder", "shortest_name_length": 11}
{"curie": "MONDO:0007709", "names": ["BFH", "TMN", "benign familial hematuria", "THIN MEMBRANE NEPHROPATHY", "Benign familial hematuria", "Thin Membrane Nephropathy", "thin membrane nephropathy", "Hematuria, Benign Familial", "hematuria, benign familial", "HEMATURIA, BENIGN FAMILIAL", "Benign familial haematuria", "hematuria, familial benign", "HEMATURIA, BENIGN RECURRENT", "thin basement membrane disease", "Thin basement membrane disease", "THIN-BASEMENT-MEMBRANE NEPHROPATHY", "Benign familial hematuria syndrome", "Thin-Basement-Membrane Nephropathy", "thin basement membrane nephropathy", "thin-basement-membrane nephropathy", "Thin basement membrane nephropathy", "benign familial hematuria (diagnosis)", "Thin basement membrane disease (disorder)", "thin basement membrane disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hematuria, benign familial", "shortest_name_length": 3}
{"curie": "MONDO:0005279", "names": ["PE", "Embolism lung", "lung embolism", "Lung embolism", "Pulmonary emboli", "Pulmonary Embolus", "Embolus pulmonary", "Pulmonary embolus", "pulmonary embolus", "EMBOLUS PULMONARY", "Emboli, pulmonary", "PULMONARY EMBOLUS", "Pulmonary Embolism", "pulmonary embolism", "PULMONARY EMBOLISM", "Pulmonary embolism", "Embolism;pulmonary", "EMBOLISM PULMONARY", "Embolism pulmonary", "EMBOLISM, PULMONARY", "Pulmonary Embolisms", "embolism, pulmonary", "Blood Clot in Lungs", "embolism; pulmonary", "pulmonary embolisms", "Embolism, Pulmonary", "pulmonary; embolism", "Embolisms, Pulmonary", "Pulmonary embolism NOS", "PE (pulmonary embolism)", "Blood clots in the lung", "PE - Pulmonary embolism", "Blood Clots in the Lung", "Pulmonary artery embolism", "pulmonary artery embolism", "Blood clot in artery of lung", "pulmonary embolism (disease)", "Pulmonary embolism (disorder)", "pulmonary embolism (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary embolism", "shortest_name_length": 2}
{"curie": "MONDO:0009901", "names": ["BPS", "BPS1", "Bartsocas-Papas Syndrome", "Bartsocas-Papas syndrome", "Bartsocas Papas syndrome", "BARTSOCAS-PAPAS SYNDROME 1", "Bartsocas-Papas syndrome 1", "pterygium popliteal lethal type", "pterygium, popliteal, lethal type", "Pterygium, Popliteal, Lethal Type", "PTERYGIUM, POPLITEAL, LETHAL TYPE", "Aslan Multiple Pterygium Syndrome", "lethal popliteal pterygium syndrome", "Lethal popliteal pterygium syndrome", "Multiple Pterygium Syndrome, Aslan Type", "MULTIPLE PTERYGIUM SYNDROME, ASLAN TYPE", "multiple pterygium syndrome, Aslan type", "popliteal pterygium syndrome lethal type", "Popliteal Pterygium Syndrome, Lethal Type", "POPLITEAL PTERYGIUM SYNDROME, LETHAL TYPE", "popliteal pterygium syndrome, lethal type", "Autosomal recessive popliteal pterygium syndrome", "autosomal recessive popliteal pterygium syndrome", "Autosomal Recessive Popliteal Pterygium Syndrome", "popliteal pterygium syndrome, Bartsocas-Papas type", "popliteal pterygium syndrome, Bartsocas-Papas type 1", "POPLITEAL PTERYGIUM SYNDROME, BARTSOCAS-PAPAS TYPE 1", "Autosomal recessive popliteal pterygium syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bartsocas-Papas syndrome 1", "shortest_name_length": 3}
{"curie": "UMLS:C4683566", "names": ["Lugano Classification Limited Stage Adult Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Limited Stage Adult Lymphoma AJCC v8", "shortest_name_length": 58}
{"curie": "UMLS:C0086533", "names": ["Leiomyoblastoma", "Leiomyoblastomas", "Epithelioid Leiomyoma", "Epithelioid leiomyoma", "Leiomyoma, Epithelioid", "Epithelioid Leiomyomas", "Stout's Leiomyoblastoma", "Leiomyomas, Epithelioid", "Epithelioid Cell Type GIST", "Epithelioid leiomyoma (morphologic abnormality)", "Epithelioid Cell Type Gastrointestinal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leiomyoma, Epithelioid", "shortest_name_length": 15}
{"curie": "MONDO:0015792", "names": ["THOP", "hypothyroxinemia of prematurity", "Hypothyroxinemia of Prematurity", "Hypothyroxinemia of prematurity", "Hypothyroxinaemia of prematurity", "Hypothyroxinemia of preterm birth", "Transient Congenital Hypothyroidism", "transient congenital hypothyroidism", "Transient congenital hypothyroidism", "Transient Hypothyroxinemia of Prematurity", "Transient hypothyroxinemia of prematurity", "transient hypothyroxinemia of prematurity", "Hypothyroxinemia of prematurity (disorder)", "Transient hypothyroxinaemia of prematurity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transient congenital hypothyroidism", "shortest_name_length": 4}
{"curie": "UMLS:C0857812", "names": ["Sickle-cell beta thalassemia", "Sickle-cell beta thalassaemia", "Sickle cell beta plus thalassemia", "Sickle cell beta plus thalassaemia", "sickle cell Hb-S Beta plus thalassemia", "Sickle cell beta plus thalassemia (disorder)", "sickle cell Hb-S Beta plus thalassemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sickle cell beta plus thalassemia", "shortest_name_length": 28}
{"curie": "UMLS:C1336398", "names": ["Stage IVC Salivary Gland Cancer", "Stage IVC Major Salivary Gland Cancer", "Stage IVC Major Salivary Gland Carcinoma", "Stage IVC Major Salivary Gland Cancer AJCC v7", "Stage IVC Major Salivary Gland Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Major Salivary Gland Cancer AJCC v7", "shortest_name_length": 31}
{"curie": "UMLS:C1709833", "names": ["Radiation sickness syndrome", "Radiation Sickness Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radiation sickness syndrome", "shortest_name_length": 27}
{"curie": "MONDO:0030746", "names": ["JEB2A", "epidermolysis bullosa, junctional 2A, intermediate", "EPIDERMOLYSIS BULLOSA, JUNCTIONAL 2A, INTERMEDIATE", "epidermolysis bullosa, junctional 2A, non-herlitz IIA", "EPIDERMOLYSIS BULLOSA, JUNCTIONAL 2A, NON-HERLITZ TYPE", "epidermolysis bullosa, junctional 2A, generalized intermediate", "EPIDERMOLYSIS BULLOSA, JUNCTIONAL 2A, GENERALIZED INTERMEDIATE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolysis bullosa, junctional 2A, intermediate", "shortest_name_length": 5}
{"curie": "MONDO:0015822", "names": ["acquired neutropenia", "immunologic neutropenia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired neutropenia", "shortest_name_length": 20}
{"curie": "MONDO:0007456", "names": ["Diarrhea, Glucose-Stimulated Secretory, with Common Variable Immunodeficiency", "diarrhea, glucose-stimulated secretory, with common variable immunodeficiency", "DIARRHEA, GLUCOSE-STIMULATED SECRETORY, WITH COMMON VARIABLE IMMUNODEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diarrhea, glucose-stimulated secretory, with common variable immunodeficiency", "shortest_name_length": 77}
{"curie": "MONDO:0019533", "names": ["PCH", "Cold hemoglobinuria", "cold hemoglobinuria", "Cold haemoglobinuria", "cold; hemoglobinuria", "hemoglobinuria; cold", "Donath-Landsteiner syndrome", "Cold paroxysmal hemoglobinuria", "paroxysmal cold hemoglobinuria", "Paroxysmal Cold Hemoglobinuria", "Cold Paroxysmal Hemoglobinuria", "Cold agglutinin hemoglobinuria", "Paroxysmal cold hemoglobinuria", "hemoglobinuria paroxysmal cold", "Paroxysmal Hemoglobinuria, Cold", "Hemoglobinuria, Paroxysmal Cold", "Hemoglobinuria, Cold Paroxysmal", "Cold agglutinin haemoglobinuria", "paroxysmal cold haemoglobinuria", "Paroxysmal cold haemoglobinuria", "Donath-Landsteiner hemolytic anemia", "PCH - Paroxysmal cold hemoglobinuria", "PCH - Paroxysmal cold haemoglobinuria", "hemolytic paroxysmal cold hemoglobinuria", "Paroxysmal cold hemoglobinuria (disorder)", "hemolytic anemia due to paroxysmal cold hemoglobinuria", "Cold Donath Landsteiner type autoimmune hemolytic anemia", "Cold Donath Landsteiner type autoimmune haemolytic anaemia", "hemolytic anemia due to paroxysmal cold hemoglobinuria (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paroxysmal cold hemoglobinuria", "shortest_name_length": 3}
{"curie": "UMLS:C5418573", "names": ["Advanced Malignant Head and Neck Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Malignant Head and Neck Neoplasm", "shortest_name_length": 41}
{"curie": "UMLS:C1332643", "names": ["Burkitt Lymphoma PTLD", "Burkitt's Lymphoma PTLD", "Burkitt Lymphoma Post-Transplant Lymphoproliferative Disorder", "Burkitt's Lymphoma Post-Transplant Lymphoproliferative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Burkitt Lymphoma Post-Transplant Lymphoproliferative Disorder", "shortest_name_length": 21}
{"curie": "UMLS:C4763831", "names": ["Metastatic Lipid Rich Urothelial Carcinoma", "Metastatic Lipid Rich Bladder Urothelial Carcinoma", "Metastatic Lipid-Cell Urothelial Carcinoma of the Bladder", "Metastatic Infiltrating Bladder Urothelial Carcinoma, Lipid-Cell Variant", "Metastatic Infiltrating Bladder Urothelial Carcinoma, Lipid-Rich Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Infiltrating Bladder Urothelial Carcinoma, Lipid-Rich Variant", "shortest_name_length": 42}
{"curie": "UMLS:C4525435", "names": ["Ampulla of Vater Cancer by AJCC v8 Stage", "Ampulla of Vater Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ampulla of Vater Cancer by AJCC v8 Stage", "shortest_name_length": 40}
{"curie": "MONDO:0019175", "names": ["primary lymphedema", "Primary Lymphedema", "Troncular lymphatic malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary lymphedema", "shortest_name_length": 18}
{"curie": "UMLS:C3273251", "names": ["Sclerosing Polycystic Adenosis", "Salivary Gland Sclerosing Polycystic Adenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sclerosing Polycystic Adenosis", "shortest_name_length": 30}
{"curie": "MONDO:0020203", "names": ["pigmented conjunctival lesion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pigmented conjunctival lesion", "shortest_name_length": 29}
{"curie": "MONDO:0024300", "names": ["Phosphopenic Rickets", "Phosphopenic rickets", "hypophosphatemic Ricket", "Hypophosphatemic Ricket", "Hypophosphatemic rickets", "Hypophosphatemic Rickets", "Ricket, hypophosphatemic", "hypophosphatemic rickets", "Ricket, Hypophosphatemic", "Rickets, Hypophosphatemic", "Phosphopenic type rickets", "Hypophosphataemic rickets", "hypophosphatemia in rickets", "vitamin D-resistant rickets", "rickets, vitamin D resistant", "rickets, vitamin D-resistant", "Phosphopenic type rickets (disorder)", "hypophosphatemic rickets (diagnosis)", "acquired vitamin D-resistant rickets", "acquired vitamin D resistant rickets", "hypophosphatemic vitamin D-resistant rickets", "hypophosphatemic vitamin D resistant rickets", "hypophosphatemia, vitamin D-resistant rickets"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypophosphatemic rickets", "shortest_name_length": 20}
{"curie": "UMLS:C4329736", "names": ["Distal monosomy 18q", "Distal 18q deletion syndrome", "Distal 18q Deletion Syndrome", "Distal chromosome 18q deletion syndrome", "Distal chromosome 18q deletion syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Distal chromosome 18q deletion syndrome", "shortest_name_length": 19}
{"curie": "UMLS:C1334266", "names": ["Bladder Urothelial Proliferation of Uncertain Malignant Potential"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder Urothelial Proliferation of Uncertain Malignant Potential", "shortest_name_length": 65}
{"curie": "MONDO:0011715", "names": ["SCKL2", "SECKEL SYNDROME 2", "Seckel syndrome 2", "RBBP8 Seckel syndrome", "Seckel syndrome type 2", "Seckel-type dwarfism 2", "SECKEL-TYPE DWARFISM 2", "Bird-headed dwarfism 2", "microcephalic primordial dwarfism 2", "Microcephalic primordial dwarfism 2", "MICROCEPHALIC PRIMORDIAL DWARFISM 2", "Seckel syndrome caused by mutation in RBBP8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Seckel syndrome 2", "shortest_name_length": 5}
{"curie": "MONDO:0004420", "names": ["breast malignant spiradenoma", "Malignant Breast Spiradenoma", "malignant spiradenoma of breast", "Malignant Breast Eccrine Spiradenoma", "breast malignant eccrine spiradenoma", "malignant breast eccrine spiradenoma", "Malignant Eccrine Spiradenoma of Breast", "malignant eccrine spiradenoma of breast", "malignant Eccrine Spiradenoma of the breast", "Malignant Eccrine Spiradenoma of the Breast", "malignant eccrine spiradenoma of the breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast malignant eccrine spiradenoma", "shortest_name_length": 28}
{"curie": "MONDO:0007414", "names": ["GSD", "Gorham disease", "Gorham Disease", "gorham disease", "disease gorhams", "Gorhams Disease", "Gorham syndrome", "Gorham's disease", "gorham's disease", "Gorham's Disease", "Massive Osteolysis", "Massive osteolysis", "Massive Osteolyses", "osteolysis massive", "massive osteolysis", "osteolysis, massive", "Osteolysis, Massive", "OSTEOLYSIS, MASSIVE", "Gorham Stout Disease", "GORHAM-STOUT DISEASE", "Gorham-Stout Disease", "Phantom bone disease", "Gorham-Stout disease", "vanishing bone disease", "Vanishing bone disease", "osteolysis Gorham's disease", "Gorham's disease (disorder)", "Hemangiomata with osteolysis", "Gorham's disease (diagnosis)", "Idiopathic massive osteolysis", "Haemangiomata with osteolysis", "idiopathic massive osteolysis", "Progressive massive osteolysis", "progressive massive osteolysis", "Osteolysis and angiomatous nevi", "Osteolysis and angiomatous naevi", "cystic angiomatosis of bone diffuse", "CYSTIC ANGIOMATOSIS OF BONE, DIFFUSE", "cystic angiomatosis of bone, diffuse", "Cystic Angiomatosis Of Bone, Diffuse"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gorham-Stout disease", "shortest_name_length": 3}
{"curie": "UMLS:C0858678", "names": ["Alopecia reversible"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alopecia reversible", "shortest_name_length": 19}
{"curie": "MONDO:0002845", "names": ["Necrotizing Gastritis", "Necrotizing gastritis", "Necrotising gastritis", "necrotizing gastritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "necrotizing gastritis", "shortest_name_length": 21}
{"curie": "MONDO:0009336", "names": ["hemosiderosis, pulmonary, with deficiency of gamma-a globulin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemosiderosis, pulmonary, with deficiency of gamma-a globulin", "shortest_name_length": 61}
{"curie": "UMLS:C0333514", "names": ["Zonal necrosis", "Zonal Necrosis", "Necrosis, zonal", "Zonal necrosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Zonal necrosis", "shortest_name_length": 14}
{"curie": "UMLS:C1336155", "names": ["Stage IIA Bone Sarcoma", "Stage IIA Sarcoma of Bone", "Stage IIA Sarcoma of the Bone", "Stage IIA Bone Sarcoma AJCC v7", "Stage IIA Bone Sarcoma  AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Bone Sarcoma AJCC v7", "shortest_name_length": 22}
{"curie": "UMLS:C4524186", "names": ["DEL", "Double Expressor Lymphoma", "Double expressor lymphoma", "Double-Expressor Lymphoma", "Double-Expressing Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Double-Expressor Lymphoma", "shortest_name_length": 3}
{"curie": "MONDO:0024656", "names": ["Colorectal Lymphoma", "colorectal lymphoma", "large intestine lymphoma", "Large Intestinal Lymphoma", "large intestinal lymphoma", "Primary Colorectal Lymphoma", "primary colorectal lymphoma", "lymphoma of large intestine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorectal lymphoma", "shortest_name_length": 19}
{"curie": "UMLS:C0521616", "names": ["pseudoporphyria", "Pseudoporphyria", "Pseudoporphyria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pseudoporphyria", "shortest_name_length": 15}
{"curie": "UMLS:C1334422", "names": ["Grade I Corneal Intraepithelial Neoplasia", "Grade 1 Corneal Intraepithelial Neoplasia", "Low Grade Corneal Intraepithelial Neoplasia", "Low Grade Corneal Squamous Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Grade Corneal Squamous Intraepithelial Neoplasia", "shortest_name_length": 41}
{"curie": "UMLS:C0750993", "names": ["Schizophreniform Catatonia", "Catatonia, Schizophreniform", "Schizophreniform Catatonias", "Catatonias, Schizophreniform"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Schizophreniform Catatonia", "shortest_name_length": 26}
{"curie": "MONDO:0001400", "names": ["ureter schwannoma", "Ureter Schwannoma", "ureter neurilemmoma", "Ureter Neurilemmoma", "Ureteral Schwannoma", "ureteral schwannoma", "schwannoma of ureter", "Schwannoma of Ureter", "ureteral neurilemmoma", "Ureteral Neurilemmoma", "neurilemmoma of ureter", "Neurilemmoma of Ureter", "Schwannoma of the Ureter", "schwannoma of the ureter", "neurilemmoma of the ureter", "Neurilemmoma of the Ureter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schwannoma of ureter", "shortest_name_length": 17}
{"curie": "UMLS:C0340359", "names": ["Prosthetic Valve Endocarditis", "endocarditis prosthetic valve", "Prosthetic valve endocarditis", "prosthetic valve endocarditis", "PVE - Prosthetic valve endocarditis", "Prosthetic valve endocarditis (disorder)", "prosthetic valve endocarditis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prosthetic valve endocarditis", "shortest_name_length": 29}
{"curie": "MONDO:0015681", "names": ["Heller syndrome", "heller syndrome", "heller's syndrome", "Heller's syndrome", "symbiotic psychosis", "Dementia infantilis", "Dementia infantalis", "dementia infantilis", "Symbiotic psychosis", "Disintegrative psychosis", "disintegrative psychosis", "Psychosis disintegrative", "psychosis; disintegrative", "disintegrative; psychosis", "childhood disintegrative disease", "childhood disintegrative disorder", "Childhood disintegrative disorder", "Childhood Disintegrative Disorder", "disintegrative psychosis; childhood", "CDD - Childhood disintegrative disorder", "Childhood disintegrative disorder (disorder)", "childhood disintegrative disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood disintegrative disorder", "shortest_name_length": 15}
{"curie": "MONDO:0003630", "names": ["pancreas serous adenocarcinoma", "Pancreatic Serous Cystadenocarcinoma", "Pancreatic serous cystadenocarcinoma", "pancreatic serous cystadenocarcinoma", "serous cystadenocarcinoma of pancreas", "Serous cystadenocarcinoma of pancreas", "Serous Cystadenocarcinoma of Pancreas", "serous cystadenocarcinoma of the pancreas", "Serous Cystadenocarcinoma of the Pancreas", "Serous cystadenocarcinoma of pancreas (disorder)", "serous cystadenocarcinoma of pancreas (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic serous cystadenocarcinoma", "shortest_name_length": 30}
{"curie": "UMLS:C5239394", "names": ["Recurrent Primary Central Nervous System Tumor", "Recurrent Primary Central Nervous System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Primary Central Nervous System Neoplasm", "shortest_name_length": 46}
{"curie": "MONDO:0012562", "names": ["HPE7", "holoprosencephaly 7", "Holoprosencephaly 7", "HOLOPROSENCEPHALY 7", "PTCH1 holoprosencephaly", "holoprosencephaly type 7", "holoprosencephaly caused by mutation in PTCH1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "holoprosencephaly 7", "shortest_name_length": 4}
{"curie": "UMLS:C0740766", "names": ["acute pneumonia", "PNEUMONIA ACUTE", "Acute pneumonia", "ACUTE PNEUMONIA", "Acute Pneumonia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute pneumonia", "shortest_name_length": 15}
{"curie": "UMLS:C0376618", "names": ["Endotoxemia", "endotoxemia", "endotoxaemia", "Endotoxemias", "Endotoxaemia", "Endotoxemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endotoxemia", "shortest_name_length": 11}
{"curie": "MONDO:0013245", "names": ["ADMFD", "ITCH E3 ubiquitin ligase deficiency", "syndromic multisystem autoimmune disease", "autoimmune disease, syndromic multisystem", "AUTOIMMUNE DISEASE, MULTISYSTEM, WITH FACIAL DYSMORPHISM", "autoimmune disease, multisystem, with facial dysmorphism", "syndromic multisystem autoimmune disease due to ITCH deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic multisystem autoimmune disease due to ITCH deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C3897534", "names": ["Stage III Anaplastic Large Cell Lymphoma", "stage III childhood anaplastic large cell lymphoma", "Stage III Childhood Anaplastic Large Cell Lymphoma", "Ann Arbor Stage III Childhood Anaplastic Large Cell Lymphoma", "Ann Arbor Stage III Noncutaneous Childhood Anaplastic Large Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Childhood Anaplastic Large Cell Lymphoma", "shortest_name_length": 40}
{"curie": "MONDO:0004526", "names": ["Stromomyoma", "Uterine Corpus Soft Tissue Neoplasm", "uterine corpus soft tissue neoplasm", "Mixed Endometrial Stromal and Smooth Muscle Tumor", "mixed endometrial stromal and smooth muscle tumor", "Mixed Endometrial Stromal and Smooth Muscle Neoplasm", "mixed endometrial stromal and smooth muscle neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed endometrial stromal and smooth muscle tumor", "shortest_name_length": 11}
{"curie": "MONDO:0001918", "names": ["Epiphora due to excess lacrimation", "epiphora due to excess lacrimation", "Epiphora due to excess lacrimation (disorder)", "epiphora due to excess lacrimation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epiphora due to excess lacrimation", "shortest_name_length": 34}
{"curie": "MONDO:0007230", "names": ["bod syndrome", "BOD SYNDROME", "BOD syndrome", "Senior syndrome", "Brachymorphism onychodysplasia dysphalangism syndrome", "BRACHYMORPHISM-ONYCHODYSPLASIA-DYSPHALANGISM SYNDROME", "Brachymorphism-onychodysplasia-dysphalangism syndrome", "BOD (brachymorphism, onychodysplasia, dysphalangism) syndrome", "Brachymorphism with onychodysplasia and dysphalangism syndrome", "brachymorphism with onychodysplasia and dysphalangism syndrome", "Brachymorphism with onychodysplasia and dysphalangism syndrome (disorder)", "brachymorphism with onychodysplasia and dysphalangism syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brachymorphism-onychodysplasia-dysphalangism syndrome", "shortest_name_length": 12}
{"curie": "UMLS:C0854974", "names": ["Stage III Adenosquamous Lung Cancer", "Stage III Adenosquamous Lung Carcinoma", "Adenosquamous cell lung cancer stage III", "Stage III Adenosquamous Cell Lung Carcinoma", "Stage III Adenosquamous Cell Carcinoma of Lung", "Stage III Lung Adenosquamous Carcinoma AJCC v7", "Stage III Adenosquamous Cell Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenosquamous cell lung cancer stage III", "shortest_name_length": 35}
{"curie": "UMLS:C1167959", "names": ["Device ineffective"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Device ineffective", "shortest_name_length": 18}
{"curie": "UMLS:C5446939", "names": ["Unresectable Biliary Tract Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Biliary Tract Carcinoma", "shortest_name_length": 36}
{"curie": "MONDO:0009608", "names": ["Oasthouse disease", "Oast-house disease", "Beery-baby syndrome", "Smith-strang disease", "Smith-Strang disease", "SMITH-STRANG DISEASE", "Smith-Strang Disease", "OASTHOUSE URINE DISEASE", "oasthouse urine disease", "Oasthouse Urine Disease", "Oasthouse urine disease", "Oast-house urine disease", "oast-house-urine disease", "oast-house-urine; disease", "Methionine malabsorption syndrome", "Methionine Malabsorption Syndrome", "Familial methionine malabsorption", "methionine malabsorption syndrome", "METHIONINE MALABSORPTION SYNDROME", "Oasthouse urine disease (diagnosis)", "Familial methionine malabsorption (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "methionine malabsorption syndrome", "shortest_name_length": 17}
{"curie": "UMLS:C2987169", "names": ["Pancreatic Serous Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Serous Adenoma", "shortest_name_length": 25}
{"curie": "MONDO:0006337", "names": ["endometriosis ovary", "ovary; endometriosis", "endometriosis; ovary", "ovarian endometriosis", "endometriosis ovaries", "Ovarian Endometriosis", "Endometriosis of ovary", "endometriosis of ovary", "Endometriosis of ovary NOS", "ovary endometriosis (disease)", "endometriosis (disease) of ovary", "ovarian endometriosis (diagnosis)", "Endometriosis of ovary (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian endometriosis", "shortest_name_length": 19}
{"curie": "MONDO:0013059", "names": ["AGS5", "Aicardi-Goutieres Syndrome 5", "AICARDI-GOUTIERES SYNDROME 5", "Aicardi-Goutieres syndrome 5", "Aicardi-Goutieres syndrome type 5", "SAMHD1 Aicardi-Goutieres syndrome", "SAMHD1-related Aicardi-Goutieres syndrome", "Aicardi-Goutieres syndrome, autosomal dominant", "Aicardi-Goutieres syndrome caused by mutation in SAMHD1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aicardi-Goutieres syndrome 5", "shortest_name_length": 4}
{"curie": "MONDO:0009668", "names": ["LMPS", "lethal multiple pterygium syndrome", "Lethal multiple pterygium syndrome", "Lethal Multiple Pterygium Syndrome", "multiple pterygium syndrome lethal type", "Multiple pterygium syndrome lethal type", "pterygium syndrome multiple lethal type", "Multiple Pterygium Syndrome, Lethal Type", "MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE", "Pterygium Multiple syndrome, lethal type", "multiple pterygium syndrome, lethal type", "Pterygium Syndrome, Multiple, Lethal Type", "PTERYGIUM SYNDROME, MULTIPLE, LETHAL TYPE", "pterygium syndrome, multiple, lethal type", "Lethal multiple pterygium syndrome (disorder)", "Autosomal recessive lethal multiple pterygium syndrome", "autosomal recessive lethal multiple pterygium syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal multiple pterygium syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0016620", "names": ["PDP", "PHO", "PHOAR1", "UEHLINGER SYNDROME", "Roy-Jutras syndrome", "Uehlinger's syndrome", "Pachydermoperiostosis", "pachydermoperiostosis", "PDP, AUTOSOMAL RECESSIVE", "PHO, AUTOSOMAL RECESSIVE", "Friedrich-Erb-Arnold syndrome", "Pachydermoperiostosis of nail", "pachydermoperiostosis of nail", "Touraine-Solente-Gole syndrome", "TOURAINE-SOLENTE-GOLE SYNDROME", "Touraine-Solente-Golé syndrome", "Touraine Solente Gole syndrome", "Touraine Solente Gole Syndrome", "Pachydermoperiostosis syndrome", "pachydermoperiostosis syndrome", "Touraine-Solente-Gole Syndrome", "pachydermoperiostosis (diagnosis)", "Clubbed nail pachydermoperiostosis", "Marie-Bamberger syndrome, idiopathic", "hypertropic osteoarthropathy, primary", "Primary Hypertrophic Osteoarthropathy", "Primary hypertrophic osteoarthropathy", "primary hypertrophic osteoarthropathy", "Hypertrophic Osteoarthropathy, Primary", "Osteoarthropathy, primary hypertrophic", "Osteoarthropathy, Primary Hypertrophic", "hypertrophic osteoarthropathy, primary", "Pachydermoperiostosis of nail (disorder)", "Idiopathic Hypertrophic Osteoarthropathy", "Idiopathic hypertrophic osteoarthropathy", "idiopathic hypertrophic osteoarthropathy", "Hypertrophic Osteoarthropathy, Idiopathic", "Pachydermoperiostosis syndrome (disorder)", "pachydermoperiostosis of nail [ambiguous]", "Osteoarthropathy, Idiopathic Hypertrophic", "Autosomal Recessive Pachydermoperiostosis", "Pachydermoperiostosis, Autosomal Recessive", "Recessive Pachydermoperiostosis, Autosomal", "PACHYDERMOPERIOSTOSIS, AUTOSOMAL RECESSIVE", "Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive", "hypertrophic osteoarthropathy, primary, autosomal recessive, 1", "hypertrophic osteoarthropathy, primary, autosomal recessive, type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary hypertrophic osteoarthropathy", "shortest_name_length": 3}
{"curie": "UMLS:C1333797", "names": ["Digestive System Hodgkin Lymphoma", "Gastrointestinal Hodgkin Lymphoma", "Gastrointestinal Hodgkin's Lymphoma", "Primary Digestive System Hodgkin Lymphoma", "Primary Gastrointestinal Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Digestive System Hodgkin Lymphoma", "shortest_name_length": 33}
{"curie": "MONDO:0002396", "names": ["Nephrogenic Adenofibroma", "Nephrogenic adenofibroma", "nephrogenic adenofibroma", "Metanephric adenofibroma", "metanephric adenofibroma", "Metanephric Adenofibroma", "Nephrogenic adenofibroma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrogenic adenofibroma", "shortest_name_length": 24}
{"curie": "UMLS:C4688372", "names": ["Refractory Malignant Thymoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Malignant Thymoma", "shortest_name_length": 28}
{"curie": "MONDO:0009496", "names": ["Burton Syndrome", "burton syndrome", "BURTON SYNDROME", "Kniest-like dysplasia with pursed lips and ectopia lentis", "KNIEST-LIKE DYSPLASIA WITH PURSED LIPS AND ECTOPIA LENTIS", "Kniest-Like Dysplasia with Pursed Lips and Ectopia Lentis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kniest-like dysplasia with pursed lips and ectopia lentis", "shortest_name_length": 15}
{"curie": "MONDO:0014018", "names": ["SPG54", "hereditary spastic paraplegia 54", "hereditary spastic paraplegia type 54", "autosomal recessive spastic paraplegia 54", "SPASTIC PARAPLEGIA 54, AUTOSOMAL RECESSIVE", "spastic paraplegia 54, autosomal recessive", "autosomal recessive spastic paraplegia type 54", "Autosomal recessive spastic paraplegia type 54", "DDHD2 autosomal recessive complex spastic paraplegia", "familial spastic paraplegia autosomal recessive type 54", "Autosomal recessive spastic paraplegia type 54 (disorder)", "Autosomal recessive spastic paraplegia type 54 (diagnosis)", "autosomal recessive complex spastic paraplegia caused by mutation in DDHD2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 54", "shortest_name_length": 5}
{"curie": "MONDO:0009398", "names": ["HPMRS1", "GPIBD2", "MABRY SYNDROME", "Mabry syndrome", "glycosylphosphatidylinositol biosynthesis defect 2", "GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 2", "hyperphosphatasia with mental retardation syndrome 1", "PIGV hyperphosphatasia-intellectual disability syndrome", "hyperphosphatasia with mental retardation syndrome type 1", "hyperphosphatasia with intellectual disability syndrome 1", "hyperphosphatasia with intellectual disability syndrome type 1", "HYPERPHOSPHATASIA WITH IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME 1", "hyperphosphatasia with impaired intellectual development syndrome 1", "hyperphosphatasia-intellectual disability syndrome caused by mutation in PIGV"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperphosphatasia with intellectual disability syndrome 1", "shortest_name_length": 6}
{"curie": "UMLS:C3640068", "names": ["Unilateral Optic Nerve Hypoplasia", "Unilateral Hypoplasia of the Optic Nerve", "Hypoplasia of the Optic Nerve, Unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unilateral Optic Nerve Hypoplasia", "shortest_name_length": 33}
{"curie": "UMLS:C1710411", "names": ["Thyroid Gland Follicular Adenoma with Bizarre Nuclei"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Follicular Adenoma with Bizarre Nuclei", "shortest_name_length": 52}
{"curie": "MONDO:0011902", "names": ["CMT1F", "CMT1f", "CMT 1F", "Charcot-Marie-Tooth disease type IF", "Charcot Marie Tooth disease type 1F", "Charcot-Marie-Tooth disease type 1F", "Charcot-Marie-Tooth disease, type 1F", "Charcot-Marie-Tooth disease, Type 1F", "CHARCOT-MARIE-TOOTH DISEASE, TYPE 1F", "Charcot-Marie-Tooth neuropathy type 1F", "Charcot-Marie-Tooth neuropathy, type 1F", "NEFL Charcot-Marie-Tooth disease type 1", "Charcot-Marie-Tooth Neuropathy, Type 1f", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 1F", "Charcot-Marie-Tooth disease type IF (disorder)", "Charcot-Marie-Tooth disease type 1F (diagnosis)", "CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1F", "Charcot-Marie-Tooth disease, demyelinating, Type 1F", "Charcot-Marie-Tooth disease, demyelinating, type 1F", "Charcot-Marie-Tooth disease type 1 caused by mutation in NEFL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 1F", "shortest_name_length": 5}
{"curie": "UMLS:C1514507", "names": ["Prostate Basal Cell Carcinoma", "Basal Cell Carcinoma of the Prostate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Basal Cell Carcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0018489", "names": ["anti-IgLON5 disease", "Anti-IgLON5 disease", "anti-IgLON5 syndrome", "Anti-IgLON5 syndrome", "autoimmune encephalopathy with parasomnia and obstructive sleep apnea", "Autoimmune encephalopathy with parasomnia and obstructive sleep apnea", "Autoimmune encephalopathy with parasomnia and obstructive sleep apnoea", "Autoimmune encephalopathy with parasomnia and obstructive sleep apnea (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune encephalopathy with parasomnia and obstructive sleep apnea", "shortest_name_length": 19}
{"curie": "MONDO:0002514", "names": ["hepatobiliary tumor", "Hepatobiliary Tumor", "hepato-biliary tumor", "Hepato-Biliary Tumor", "hepatobiliary tumors", "Hepatobiliary Tumors", "Hepatobiliary Neoplasm", "hepatobiliary neoplasm", "Hepatobiliary neoplasm", "Hepatobiliary neoplasms", "hepato-biliary neoplasm", "Hepato-Biliary Neoplasm", "hepatic and biliary tumors", "Liver and Biliary Neoplasm", "Hepatic and Biliary Tumors", "hepatobiliary system tumor", "Hepatobiliary neoplasm NOS", "liver and biliary neoplasm", "hepatobiliary system cancer", "Hepatic and Biliary Neoplasms", "hepatobiliary benign neoplasm", "tumor of hepatobiliary system", "hepatobiliary system neoplasm", "hepatic and biliary neoplasms", "neoplasm of hepatobiliary system", "Liver and Biliary System Neoplasm", "liver and biliary system neoplasm", "hepatobiliary system neoplasm (disease)", "Hepatic, Biliary, and Gallbladder Neoplasms", "hepatic, biliary, and gallbladder neoplasms"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatobiliary neoplasm", "shortest_name_length": 19}
{"curie": "UMLS:C5420438", "names": ["Maxillofacial Chondromyxoid Fibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Maxillofacial Chondromyxoid Fibroma", "shortest_name_length": 35}
{"curie": "MONDO:0013485", "names": ["SCA35", "spinocerebellar ataxia 35", "SPINOCEREBELLAR ATAXIA 35", "spinocerebellar ataxia type 35", "Spinocerebellar ataxia type 35", "Spinocerebellar ataxia type 35 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia type 35", "shortest_name_length": 5}
{"curie": "MONDO:0001206", "names": ["aqueous misdirection", "misdirection aqueous", "Aqueous misdirection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aqueous misdirection", "shortest_name_length": 20}
{"curie": "MONDO:0001928", "names": ["Septic cholangitis", "Pyogenic Cholangitis", "Suppurative cholangitis", "Cholangitis suppurative", "CHOLANGITIS SUPPURATIVE", "suppurative cholangitis", "Suppurative Cholangitis", "Suppurative cholangitis (disorder)", "suppurative cholangitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "suppurative cholangitis", "shortest_name_length": 18}
{"curie": "UMLS:C1333290", "names": ["Diffuse Follicular Lymphoma", "diffuse follicular lymphoma", "Diffuse follicle center lymphoma", "Diffuse follicle centre lymphoma", "Follicle Centre Lymphoma Diffuse", "Diffuse Follicle Centre Lymphoma", "diffuse follicular lymphoma (diagnosis)", "Diffuse follicle center lymphoma (disorder)", "malignant neoplasm nodular lymphoma diffuse follicle center"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse follicle center lymphoma", "shortest_name_length": 27}
{"curie": "UMLS:C4054360", "names": ["Partial Remission Nephrotic Syndrome Remission", "Nephrotic Syndrome-Remission, Partial Remission"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome-Remission, Partial Remission", "shortest_name_length": 46}
{"curie": "UMLS:C0582253", "names": ["fistula jejunal", "jejunal fistula", "Jejunal Fistula", "Jejunal fistula", "jejunum; fistula", "fistulas jejunal", "fistula; jejunum", "Jejunal fistula (disorder)", "Jejunal fistula (diagnosis)", "small bowel fistula jejunum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jejunal fistula", "shortest_name_length": 15}
{"curie": "UMLS:C4525094", "names": ["Stage IV Colorectal Cancer AJCC v8", "Stage IV Colorectal Carcinoma AJCC v8", "Stage IV Colorectal (Colon or Rectal) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Colorectal Cancer AJCC v8", "shortest_name_length": 34}
{"curie": "UMLS:C0334641", "names": ["Malignant Lymphoma, Large Cell, Cleaved", "Malignant lymphoma, large cleaved cell, NOS", "Malignant lymphoma, large cell, cleaved, NOS", "Diffuse malignant lymphoma - large cleaved cell", "diffuse malignant lymphoma - large cleaved cell", "Malignant lymphoma, large cell, cleaved, diffuse", "Diffuse malignant lymphoma - large cleaved cell (disorder)", "diffuse malignant lymphoma - large cleaved cell (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse malignant lymphoma - large cleaved cell", "shortest_name_length": 39}
{"curie": "MONDO:0004803", "names": ["DECD", "hypereosinophilic syndrome", "Disseminated eosinophilic collagen disease", "disseminated eosinophilic collagen disease", "Disseminated eosinophilic collagen disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disseminated eosinophilic collagen disease", "shortest_name_length": 4}
{"curie": "UMLS:C5557180", "names": ["Stage IV Cervical Cancer AJCC v9", "Stage IV Cervical Carcinoma AJCC v9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Cervical Cancer AJCC v9", "shortest_name_length": 32}
{"curie": "MONDO:0024337", "names": ["urothelium tumor", "tumor of urothelium", "urothelial neoplasm", "Urothelial Neoplasm", "urothelium neoplasm", "neoplasm of urothelium", "urothelium neoplasm (disease)", "Transitional Cell Neoplasm of the Urinary Tract", "transitional cell neoplasm of the urinary tract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urothelial neoplasm", "shortest_name_length": 16}
{"curie": "MONDO:0010444", "names": ["XLANP", "X-linked dyserythropoietic anemia", "X-linked anemia with/without neutropenia and/or platelet abnormalities", "X-linked dyserythropoetic anemia with abnormal platelets and neutropenia", "X-linked dyserythropoietic anemia with abnormal platelets and neutropenia", "ANEMIA, X-LINKED, WITH OR WITHOUT NEUTROPENIA AND/OR PLATELET ABNORMALITIES", "anemia, X-linked, with or without neutropenia and/or platelet abnormalities", "anemia, X-linked, with/without neutropenia and/or platelet abnormalities, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked dyserythropoetic anemia with abnormal platelets and neutropenia", "shortest_name_length": 5}
{"curie": "OMIM:300932", "names": ["TBGQTL", "THYROXINE-BINDING GLOBULIN QUANTITATIVE TRAIT LOCUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 6}
{"curie": "UMLS:C0302465", "names": ["Dissection of aorta, abdominal", "AORTA ABDOMINAL ANEURYSM DISSECTING", "Dissecting Abdominal Aortic Aneurysm", "Dissecting aortic aneurysm, abdominal", "Dissecting aneurysm of abdominal aorta", "aorta abdominalis; aneurysm, dissecting"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dissecting Abdominal Aortic Aneurysm", "shortest_name_length": 30}
{"curie": "UMLS:C4087121", "names": ["Non-cirrhotic portal hypertension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-cirrhotic portal hypertension", "shortest_name_length": 33}
{"curie": "MONDO:0024630", "names": ["defective phagocytic cell chemotaxis", "Defective phagocytic cell chemotaxis", "Defective phagocytic cell chemotaxis (disorder)", "defective phagocytic cell chemotaxis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "defective phagocytic cell chemotaxis", "shortest_name_length": 36}
{"curie": "MONDO:0003104", "names": ["epicardial tumor", "Epicardial tumor", "epicardium cancer", "cancer of epicardium", "Malignant Epicardial Tumor", "malignant epicardial tumor", "malignant Epicardial tumor", "malignant tumor of epicardium", "malignant epicardial neoplasm", "malignant epicardium neoplasm", "Malignant Tumor of Epicardium", "Malignant Epicardial Neoplasm", "malignant neoplasm of epicardium", "Malignant Neoplasm of Epicardium", "Malignant neoplasm of epicardium", "Malignant Tumor of the Epicardium", "malignant tumor of the epicardium", "malignant neoplasm of the epicardium", "Malignant Neoplasm of the Epicardium", "primary malignant epicardial neoplasm", "primary malignant neoplasm of epicardium", "Primary malignant neoplasm of epicardium", "malignant neoplasm of epicardium (diagnosis)", "malignant cardiac neoplasm epicardial primary", "Primary malignant neoplasm of epicardium (disorder)", "primary malignant neoplasm of epicardium (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epicardium cancer", "shortest_name_length": 16}
{"curie": "MONDO:0012449", "names": ["SCA23", "SPINOCEREBELLAR ATAXIA 23", "spinocerebellar ataxia 23", "Spinocerebellar ataxia 23", "spinocerebellar ataxia type 23", "Spinocerebellar ataxia type 23", "SCA23 Spinocerebellar ataxia 23", "Spinocerebellar ataxia type 23 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia type 23", "shortest_name_length": 5}
{"curie": "MONDO:0019322", "names": ["pemphigus vegetan", "Pemphigus vegetans", "pemphigus vegetans", "vegetans; pemphigus", "Pemphigus, vegetans", "pemphigus; vegetans", "Pemphigus vegetans (disorder)", "pemphigus vegetans (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pemphigus vegetans", "shortest_name_length": 17}
{"curie": "MONDO:0008717", "names": ["AMDH", "AMD2C", "Acromesomelic dwarfism", "acromesomelic dwarfism", "Hunter-Thompson dysplasia", "acromesomelic dysplasia-2C", "ACROMESOMELIC DYSPLASIA 2C", "AMDH ACROMESOMELIC DWARFISM", "Acromesomelic dysplasia Hunter-Thompson type", "acromesomelic dysplasia Hunter Thompson type", "Acromesomelic dysplasia Hunter Thompson type", "Acromesomelic dysplasia, Hunter-Thompson type", "acromesomelic dysplasia, Hunter-Thompson type", "Acromesomelic Dysplasia, Hunter-Thompson Type", "ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE", "acromesomelic dysplasia 2C, Hunter-Thompson type", "Acromesomelic dysplasia Hunter-Thompson type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acromesomelic dysplasia 2C, Hunter-Thompson type", "shortest_name_length": 4}
{"curie": "UMLS:C0151919", "names": ["BLADDER STENOSIS", "Stenosis bladder", "STENOSIS BLADDER", "bladder stenosis", "Bladder stenosis", "Stenosis urinary bladder", "STENOSIS URINARY BLADDER"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder stenosis", "shortest_name_length": 16}
{"curie": "MONDO:0034146", "names": ["spastic ataxia-dysarthria due to glutaminase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic ataxia-dysarthria due to glutaminase deficiency", "shortest_name_length": 55}
{"curie": "MONDO:0011984", "names": ["SD2b", "SPD2", "synpolydactyly 2", "SYNPOLYDACTYLY 2", "SD2, Debeer type", "SPD, Debeer type", "Synpolydactyly 2", "Synpolydactyly type 2", "synpolydactyly type 2", "Synpolydactyly, Debeer type", "synpolydactyly, Debeer type", "FBLN1 non-syndromic synpolydactyly", "non-syndromic synpolydactyly caused by mutation in FBLN1", "synpolydactyly, 3/3'4, associated with metacarpal and metatarsal synostoses", "SYNPOLYDACTYLY, 3/3-PRIME/4, ASSOCIATED WITH METACARPAL AND METATARSAL SYNOSTOSES", "synpolydactyly, 3/3-prime/4, associated with metacarpal and metatarsal synostoses", "Synpolydactyly, 3, 3-Prime, 4, associated with metacarpal and metatarsal synostoses"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "synpolydactyly type 2", "shortest_name_length": 4}
{"curie": "MONDO:0002772", "names": ["Intraventricular Meningioma", "intraventricular meningioma", "Intraventricular Meningiomas", "Meningioma, Intraventricular", "Meningiomas, Intraventricular", "brain ventricle meningioma (disease)", "meningioma (disease) of brain ventricle", "intraventricular meningioma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intraventricular meningioma", "shortest_name_length": 27}
{"curie": "UMLS:C1520070", "names": ["Vulvar Angiomyxoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Angiomyxoma", "shortest_name_length": 18}
{"curie": "MONDO:0011109", "names": ["Multiple epiphyseal dysplasia Lowry type", "Multiple epiphyseal dysplasia, Lowry type", "multiple epiphyseal dysplasia, Lowry type", "Multiple Epiphyseal Dysplasia with Robin Phenotype", "multiple epiphyseal dysplasia with ROBIN phenotype", "MULTIPLE EPIPHYSEAL DYSPLASIA WITH ROBIN PHENOTYPE", "Multiple epiphyseal dysplasia with Robin phenotype", "multiple epiphyseal dysplasia with Robin phenotype", "Multiple epiphyseal dysplasia Lowry type (disorder)", "epiphyseal dysplasia, multiple, with Robin phenotype", "Epiphyseal Dysplasia, Multiple, with Robin Phenotype", "EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH ROBIN PHENOTYPE", "multiple epiphyseal dysplasia, Lowry type (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple epiphyseal dysplasia, Lowry type", "shortest_name_length": 40}
{"curie": "MONDO:0005372", "names": ["Infertility;M", "INFERTILITY MALE", "Male infertility", "Male Infertility", "male infertility", "Infertility male", "Infertility, Male", "Infertility, male", "infertility; male", "Male infertility, NOS", "MALE INFERTILITY DISORDERS", "Male infertility (disorder)", "male infertility (diagnosis)", "Male infertility, unspecified", "male reproductive system infertility", "male reproductive system infertility disorder", "infertility disorder of male reproductive system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "male infertility", "shortest_name_length": 13}
{"curie": "UMLS:C5420272", "names": ["Oropharyngeal Polymorphous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oropharyngeal Polymorphous Adenocarcinoma", "shortest_name_length": 41}
{"curie": "UMLS:C5556429", "names": ["Low-Grade Endometrial Endometrioid Carcinoma", "Low Grade Endometrial Endometrioid Carcinoma", "Low Grade Endometrial Endometrioid Adenocarcinoma", "Low-Grade Endometrial Endometrioid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Grade Endometrial Endometrioid Adenocarcinoma", "shortest_name_length": 44}
{"curie": "MONDO:0013221", "names": ["MMD2", "MIYOSHI MYOPATHY 2", "Miyoshi Myopathy 2", "Miyoshi myopathy 2", "Miyoshi Muscular Dystrophy 2", "Miyoshi muscular dystrophy 2", "MIYOSHI MUSCULAR DYSTROPHY 2", "MIYOSHI muscular dystrophy 2", "MIYOSHI MUSCULAR DYSTROPHY 2 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Miyoshi muscular dystrophy 2", "shortest_name_length": 4}
{"curie": "MONDO:0008302", "names": ["CPPB1", "centra precocious puberty 1", "central precocious puberty 1", "precocious puberty, central, 1", "PRECOCIOUS PUBERTY, CENTRAL, 1", "KISS1R central precocious puberty", "precocious puberty, central, type 1", "central precocious puberty caused by mutation in KISS1R"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "centra precocious puberty 1", "shortest_name_length": 5}
{"curie": "MONDO:0014169", "names": ["DUH3", "dyschromatosis universalis hereditaria 3", "DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 3", "ABCB6 dyschromatosis universalis hereditaria", "dyschromatosis universalis hereditaria type 3", "dyschromatosis universalis hereditaria caused by mutation in ABCB6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyschromatosis universalis hereditaria 3", "shortest_name_length": 4}
{"curie": "MONDO:0003170", "names": ["Gliofibroma", "gliofibroma", "Gliofibroma (morphologic abnormality)", "gliofibroma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gliofibroma", "shortest_name_length": 11}
{"curie": "MONDO:0023197", "names": ["frontonasal dysplasia Klippel feil syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontonasal dysplasia Klippel feil syndrome", "shortest_name_length": 43}
{"curie": "MONDO:0001596", "names": ["HYPOCHONDRIA", "hypochondria", "Hypochondria", "hypochondrias", "Hypochondriasis", "hypochondriasis", "HYPOCHONDRIASIS", "hypochondriacal neurosis", "Hypochondriacal disorder", "Hypochondriacal Neurosis", "hypochondriacal disorder", "Hypochondriacal Neuroses", "Neurosis;hypochondriacal", "hypochondriasis disorder", "Hypochondriacal neurosis", "Neurosis, hypochondriacal", "hypochondriacal; disorder", "Hypochondriacal disorders", "hypochondriacal; neurosis", "Neurosis, Hypochondriacal", "neurosis; hypochondriacal", "disorder; hypochondriacal", "Hypochondriasis (disorder)", "hypochondriasis (diagnosis)", "hypochondriacal disorder (diagnosis)", "disease (or disorder); hypochondriacal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypochondriasis", "shortest_name_length": 12}
{"curie": "MONDO:0013689", "names": ["ODG3", "ovarian dysgenesis 3", "OVARIAN DYSGENESIS 3", "ovarian dysgenesis type 3", "PSMC3IP 46 XX gonadal dysgenesis", "46 XX gonadal dysgenesis caused by mutation in PSMC3IP"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian dysgenesis 3", "shortest_name_length": 4}
{"curie": "MONDO:0005393", "names": ["GOUT", "gout", "Gout", "Gouts", "gouts", "Gout NOS", "gout; in", "Gout, NOS", "chronic gout", "gout disorder", "articular gout", "gout arthritis", "ARTHRITIS GOUT", "arthritis gout", "Articular gout", "Gouty Arthritis", "tophaceous gout", "gouty arthritis", "arthritis gouty", "gout; arthritis", "arthritis; gout", "ARTHRITIS GOUTY", "Arthritis gouty", "GOUTY ARTHRITIS", "Gouty arthritis", "ARTHRITIS, GOUTY", "Arthritis, Gouty", "gout (diagnosis)", "ARTHROPATHY GOUT", "arthropathy gout", "uratic; arthritis", "Gouty arthropathy", "gouty arthropathy", "arthritis; uratic", "Gout, unspecified", "Gouty Arthritides", "tophaceous disease", "Arthritides, Gouty", "gouty; arthropathy", "arthropathy; gouty", "Articular gout, NOS", "Joints gout affected", "Gouty arthritis, NOS", "Arthritis due to gout", "arthritis due to gout", "Gouty arthropathy (disorder)", "gouty arthropathy (diagnosis)", "Joints gout affected (finding)", "Gouty arthropathy, unspecified", "Arthritis due to gout (disorder)", "arthritis due to gout (diagnosis)", "Gout, unspecified, site unspecified", "Inflammatory disorder due to increased blood urate level", "inflammatory disorder due to increased blood urate level", "Inflammatory disorder due to increased blood urate level (disorder)", "inflammatory disorder due to increased blood urate level (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gout", "shortest_name_length": 4}
{"curie": "MONDO:0007401", "names": ["HDCPH1", "Braddock-Jones-Superneau syndrome", "hydrocephalus, autosomal dominant", "HYDROCEPHALUS, AUTOSOMAL DOMINANT", "Braddock Jones Superneau syndrome", "Hydrocephalus, Autosomal Dominant", "craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome", "Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome", "sagittal craniosynostosis, Dandy-Walker malformation and hydrocephalus", "Dandy-Walker malformation with sagittal craniosynostosis and hydrocephalus", "Craniosynostosis with Dandy-Walker malformation and hydrocephalus syndrome", "Craniosynostosis with Dandy-Walker malformation and hydrocephalus syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C1541269", "names": ["Marginal zone lymphoma stage III", "stage III marginal zone lymphoma", "Stage III Marginal Zone Lymphoma", "stage III marginal zone B-cell lymphoma", "Stage III Marginal Zone B-Cell Lymphoma", "Ann Arbor Stage III Marginal Zone Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Marginal zone lymphoma stage III", "shortest_name_length": 32}
{"curie": "MONDO:0008620", "names": ["Short ulna", "Short ulnae", "ulna hypoplasia", "Ulna hypoplasia", "hypoplasia; ulna", "ULNAR HYPOPLASIA", "ulna; hypoplasia", "Ulnar hypoplasia", "ulnar hypoplasia", "Hypoplastic ulna", "Hypoplastic ulnae", "Underdeveloped ulna", "Hypoplasia of the ulna", "fryns hofkens fabry syndrome", "Fryns Hofkens Fabry syndrome", "Fryns-Hofkens-Fabry syndrome", "UPPER LIMB MESOMELIC DYSPLASIA", "upper limb mesomelic dysplasia", "Upper limb mesomelic dysplasia", "Mesomelic dysplasia of upper limb", "Underdeveloped inner large forearm bone", "Mesomelic dysplasia of upper limb (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "upper limb mesomelic dysplasia", "shortest_name_length": 10}
{"curie": "MONDO:0009243", "names": ["Fraser-Like Syndrome", "Fraser-like syndrome", "FRASER-LIKE SYNDROME", "Fused Eyelids, Airway Anomalies, Ovarian Cysts, and Digital Anomalies", "FUSED EYELIDS, AIRWAY ANOMALIES, OVARIAN CYSTS, AND DIGITAL ANOMALIES", "Fused eyelids, airway anomalies, ovarian cysts, and digital anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fraser-like syndrome", "shortest_name_length": 20}
{"curie": "UMLS:C1336220", "names": ["stage IIIB endometrial cancer", "stage IIIB uterine corpus cancer", "stage IIIB endometrial carcinoma", "Stage IIIB Uterine Corpus Cancer", "stage IIIB uterine corpus cancer AJCC v7", "Stage IIIB Uterine Corpus Cancer AJCC v7", "Stage IIIB Uterine (including Endometrial) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Uterine Corpus Cancer AJCC v7", "shortest_name_length": 29}
{"curie": "MONDO:0001029", "names": ["brevicollis", "BREVICOLLIS", "Klippel-Feil", "Klippel-feil", "Feil-Klippel", "Nielsen's disease", "Klippel-Feil anomaly", "klippel-feil syndrome", "klippel feil syndrome", "KLIPPEL-FEIL SYNDROME", "Klippel Feil Syndrome", "Klippel-Feil Syndrome", "Klippel Feil syndrome", "Klippel-Feil syndrome", "Klippel-Feil Sequence", "feil klippel syndrome", "Klippel-Feil sequence", "Syndrome, Klippel-Feil", "Klippel-Feil deformity", "Klippel-Feil; deformity", "deformity; Klippel-Feil", "Cervical Fusion Syndrome", "Cervical fusion syndrome", "CERVICAL VERTEBRA FUSION", "cervical vertebral fusion", "cervical; fusion syndrome", "Cervical-vertebral fusion", "Cervical vertebral fusion", "Klippel-Feil malformation", "fusion syndrome; cervical", "cervical; syndrome, fusion", "syndrome; cervical, fusion", "KFS - Klippel-Feil syndrome", "Isolated Klippel-Feil syndrome", "TORTICOLLIS, OSSEOUS CONGENITAL", "Cervical C2/C3 vertebral fusion", "Klippel-Feil and Turner syndrome", "Dystrophia Brevicollis Congenita", "Klippel-Feil sequence (disorder)", "Fusion of cervical vertebrae c2-3", "Congenital dystrophia brevicollis", "congenital dystrophia brevicollis", "Dystrophia Brevicollis Congenitas", "Klippel-Feil syndrome (diagnosis)", "Cervical vertebral fusion syndrome", "Congenital fused cervical segments", "Vertebral Cervical Fusion Syndrome", "Congenital cervical vertebral fusion", "autosomal dominant Klippel-Feil syndrome", "Bonnevie-Ullrich and Klippel-Feil syndrome", "congenital synostosis of cervical vertebrae", "Congenital dystrophia brevicollis (disorder)", "Klippel-Feil deformity, deafness and facial asymmetry"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Klippel-Feil syndrome", "shortest_name_length": 11}
{"curie": "UMLS:C0686546", "names": ["Burkitt tumor of spleen", "Splenic Burkitt Lymphoma", "Burkitt tumour of spleen", "Burkitt lymphoma, spleen", "Burkitt's tumor of spleen", "Splenic Burkitt's Lymphoma", "Burkitt lymphoma of spleen", "Burkitt's tumour of spleen", "Burkitt's lymphoma of spleen", "Primary Splenic Burkitt's Lymphoma", "Burkitt's tumor or lymphoma, spleen", "Burkitt's lymphoma of spleen (disorder)", "Burkitt's lymphoma of spleen (diagnosis)", "Burkitt's tumor or lymphoma involving spleen", "Burkitt's tumour or lymphoma involving spleen"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Burkitt's lymphoma of spleen", "shortest_name_length": 23}
{"curie": "MONDO:0030051", "names": ["IDDALDS", "intellectual developmental disorder with autistic features and language delay, with or without seizures", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISTIC FEATURES AND LANGUAGE DELAY, WITH OR WITHOUT SEIZURES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder with autistic features and language delay, with or without seizures", "shortest_name_length": 7}
{"curie": "MONDO:0017330", "names": ["cancer diagnosed during pregnancy", "malignancy diagnosed during pregnancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignancy diagnosed during pregnancy", "shortest_name_length": 33}
{"curie": "UMLS:C5668161", "names": ["Recurrent Extrapulmonary Small Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Extrapulmonary Small Cell Neuroendocrine Carcinoma", "shortest_name_length": 60}
{"curie": "MONDO:0004815", "names": ["Osteosclerotic Myeloma", "osteosclerotic myeloma", "Osteosclerotic myeloma", "Osteosclerotic Multiple Myeloma", "osteosclerotic multiple myeloma", "Osteosclerotic myeloma (disorder)", "Osteosclerotic myeloma (diagnosis)", "Osteosclerotic Plasma Cell Myeloma", "osteosclerotic plasma cell myeloma", "malignant neoplasm multiple myeloma osteosclerotic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteosclerotic plasma cell myeloma", "shortest_name_length": 22}
{"curie": "UMLS:C1405546", "names": ["Pseudomenses", "pseudomenstruation", "Pseudomenstruation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pseudomenstruation", "shortest_name_length": 12}
{"curie": "UMLS:C1698668", "names": ["necrosis soft tissue lower limb", "Soft tissue necrosis lower limb", "necrosis of soft tissue of lower limb", "Lower Limb Soft Tissue Necrotic Lesion", "necrosis of soft tissue of lower limb (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lower Limb Soft Tissue Necrotic Lesion", "shortest_name_length": 31}
{"curie": "MONDO:0009074", "names": ["Facial dysmorphism, macrocephaly, myopia and Dandy-Walker malformation", "facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome", "Dandy-Walker malformation with mental retardation, macrocephaly, myopia, and BRACHYTELEPHALANGY", "Dandy-walker malformation with mental retardation, macrocephaly, myopia, and brachytelephalangy", "DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, MACROCEPHALY, MYOPIA, AND BRACHYTELEPHALANGY", "Dandy-Walker malformation with intellectual disability, macrocephaly, myopia, and BRACHYTELEPHALANGY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome", "shortest_name_length": 70}
{"curie": "MONDO:0005307", "names": ["contracture", "Contracture", "CONTRACTURE", "contractures", "Contractures", "Contractures NOS", "Contracture, NOS", "contracture joint", "Joint contraction", "Joint Contracture", "joint contracture", "deformity flexion", "JOINT CONTRACTURE", "contraction joint", "flexion deformity", "Joint contracture", "Flexion deformity", "Muscle Contracture", "CONTRACTURE MUSCLE", "contracture; joint", "joint; contracture", "contractures joint", "MUSCLE CONTRACTURE", "deformity; flexion", "Muscle contracture", "flexion; deformity", "Joint contractures", "muscle contracture", "muscle; contracture", "flexion contracture", "contractures muscle", "deformities flexion", "contracture; muscle", "contracture flexion", "Flexion contracture", "Flexion deformities", "CONTRACTURE FLEXION", "flexion; contracture", "contractures flexion", "Flexion contractures", "of joint contracture", "contractures muscles", "contracture; flexion", "Contracture of joint", "contracture of joint", "Contracture of muscle", "Contracture;muscle(s)", "Contractures of joints", "Contracture of joint, NOS", "Flexion joint contractures", "Flexion deformity (disorder)", "Flexion contracture of joint", "Muscle contracture (disorder)", "flexion deformity (diagnosis)", "Flexion contractures of joints", "muscle contracture (diagnosis)", "Contracture of joint (disorder)", "contracture of joint (diagnosis)", "Flexion deformity, site unspecified", "Flexion deformity, unspecified site", "Contracture (morphologic abnormality)", "Contracture of joint, site unspecified", "Contracture of muscle, site unspecified", "Flexion contracture of joint (disorder)", "Contracture of muscle, unspecified site", "Flexed joint that cannot be straightened", "Flexion deformity (morphologic abnormality)", "Flexion contracture (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "contracture", "shortest_name_length": 11}
{"curie": "UMLS:C0398561", "names": ["Glucose Phosphate Isomerase Deficiency", "Glucose phosphate isomerase deficiency", "Glucose-6-Phosphate Isomerase Deficiency", "GPI - Glucose phosphate isomerase deficiency", "Glucose phosphate isomerase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Glucose phosphate isomerase deficiency", "shortest_name_length": 38}
{"curie": "MONDO:0004612", "names": ["Stewart's granuloma", "stewart's granuloma", "angiocentric lymphoma", "Nasal T-cell lymphoma", "malignant reticulosis", "nasal t-cell lymphoma", "Malignant reticulosis", "lymphoma nasal t-cell", "RETICULOSIS, MALIGNANT", "RETICULOSIS, ALEUKEMIC", "reticulosis; malignant", "malignant; reticulosis", "polymorphic reticulosis", "Malignant Histiocytoses", "Malignant Histiocytosis", "malignant histiocytosis", "histiocytosis malignant", "Malignant histiocytosis", "Polymorphic reticulosis", "polymorphic; reticulosis", "Histiocytoses, Malignant", "HISTIOCYTOSIS, MALIGNANT", "malignant; histiocytosis", "Histiocytosis, Malignant", "reticulosis; polymorphic", "histiocytosis; malignant", "RETICULOSIS, POLYMORPHORIC", "Malignant reticulosis, NOS", "angiocentric t-cell lymphoma", "Midline malignant reticulosis", "malignant histiocytic disease", "Malignant midline reticulosis", "malignant midline reticulosis", "Malignant Histiocytic Disorder", "Malignant histiocytic disorder", "RETICULOSIS, MALIGNANT MIDLINE", "malignant histiocytic disorder", "malignant histiocytic disorders", "Malignant Histiocytic Disorders", "Histiocytic Disorder, Malignant", "histiocytic disorder, malignant", "Malignant reticuloendotheliosis", "Disorder, Malignant Histiocytic", "malignant; reticuloendotheliosis", "Disseminated histiocytic sarcoma", "reticuloendotheliosis; malignant", "Histiocytic Disorders, Malignant", "Disorders, Malignant Histiocytic", "disorders, malignant histiocytic", "Histiocytic Medullary Reticulosis", "histiocytic medullary reticulosis", "Malignant histiocytosis (clinical)", "Malignant histiocytosis (disorder)", "malignant histiocytosis (diagnosis)", "Malignant histiocytic disorder (disorder)", "malignant histiocytic disorder (diagnosis)", "Disseminated histiocytic sarcoma (disorder)", "Malignant histiocytosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant histiocytosis", "shortest_name_length": 19}
{"curie": "MONDO:0011471", "names": ["IBD3", "inflammatory bowel disease 3", "Inflammatory Bowel Disease 3", "INFLAMMATORY BOWEL DISEASE 3", "inflammatory bowel disease type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory bowel disease 3", "shortest_name_length": 4}
{"curie": "UMLS:C1541264", "names": ["stage II marginal zone lymphoma", "Marginal zone lymphoma stage II", "Stage II Marginal Zone Lymphoma", "Stage II Marginal Zone B-Cell Lymphoma", "stage II marginal zone B-cell lymphoma", "Ann Arbor Stage II Marginal Zone Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Marginal zone lymphoma stage II", "shortest_name_length": 31}
{"curie": "UMLS:C0238707", "names": ["Attention impaired", "ATTENTION IMPAIRMENT", "Impairment of attention"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Attention impaired", "shortest_name_length": 18}
{"curie": "UMLS:C4527169", "names": ["Stage IIC Cutaneous (Skin) Melanoma", "Clinical Stage IIC Cutaneous Melanoma AJCC v8", "Clinical Stage IIC Melanoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage IIC Cutaneous Melanoma AJCC v8", "shortest_name_length": 35}
{"curie": "MONDO:0003426", "names": ["Clear cell adenoma", "Clear Cell Adenoma", "clear cell adenoma", "adenoma, clear cell, benign", "ADENOMA, CLEAR CELL, BENIGN", "clear cell adenoma (morphologic abnormality)", "Clear cell adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "clear cell adenoma", "shortest_name_length": 18}
{"curie": "UMLS:C2732473", "names": ["MIC", "DCISM", "Microinvasive Breast Carcinoma", "Ductal Carcinoma In Situ with Microinvasion", "Ductal carcinoma in situ with microinvasion", "Ductal carcinoma in situ with microinvasion (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ductal Carcinoma In Situ with Microinvasion", "shortest_name_length": 3}
{"curie": "UMLS:C4743624", "names": ["Pituitary Gland Double Adenomas", "Double PitNET/Adenomas of Distinct Lineages", "Double Pituitary Neuroendocrine Tumors of Distinct Lineages", "Double Pituitary Neuroendocrine Tumors/Adenomas of Distinct Lineages"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Double Pituitary Neuroendocrine Tumors of Distinct Lineages", "shortest_name_length": 31}
{"curie": "MONDO:0012536", "names": ["OI7", "OI type 7", "OI, type 7", "OI type VII", "OI, TYPE VII", "OI, Type VII", "OI2B, FORMERLY", "CRTAP osteogenesis imperfecta", "OI7 Osteogenesis Imperfecta 7", "osteogenesis imperfecta type 7", "Osteogenesis imperfecta, type 7", "osteogenesis imperfecta, type 7", "osteogenesis imperfecta type VII", "Osteogenesis imperfecta, type 2B", "Osteogenesis imperfecta type IIB", "Osteogenesis Imperfecta Type VII", "Osteogenesis Imperfecta, Type VII", "Osteogenesis Imperfecta, Type IIB", "osteogenesis imperfecta, type IIb", "OSTEOGENESIS IMPERFECTA, TYPE VII", "osteogenesis imperfecta, type VII", "OI type 7 Osteogenesis Imperfecta Type 7", "osteogenesis imperfecta, type IIb, formerly", "Osteogenesis imperfecta type IIB (disorder)", "OSTEOGENESIS IMPERFECTA, TYPE IIB, FORMERLY", "Osteogenesis imperfecta type IIB (diagnosis)", "OI, type 2B Osteogenesis imperfecta, type 2B", "OI type VII Osteogenesis Imperfecta Type VII", "OI, type IIB Osteogenesis imperfecta, type IIB", "osteogenesis imperfecta caused by mutation in CRTAP", "Osteogenesis imperfecta, perinatal lethal, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteogenesis imperfecta type 7", "shortest_name_length": 3}
{"curie": "MONDO:0011209", "names": ["progeroid facial appearance with hand anomalies", "Progeroid Facial Appearance with Hand Anomalies", "PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progeroid facial appearance with hand anomalies", "shortest_name_length": 47}
{"curie": "MONDO:0030472", "names": ["DEE98", "early infantile epileptic encephalopathy 98", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 98", "developmental and epileptic encephalopathy 98"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy 98", "shortest_name_length": 5}
{"curie": "MONDO:0017195", "names": ["bruck syndrome", "Bruck syndrome", "Bruck syndrome (disorder)", "osteogenesis imperfecta with congenital joint contractures", "Osteogenesis imperfecta-congenital joint contractures syndrome", "osteogenesis imperfecta-congenital joint contractures syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bruck syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C3502052", "names": ["Thrombophilia, Hereditary, Due To Protein S Deficiency, Autosomal Dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thrombophilia, Hereditary, Due To Protein S Deficiency, Autosomal Dominant", "shortest_name_length": 74}
{"curie": "MONDO:0000241", "names": ["Keshan", "Keshan disease", "Keshan; disease", "Keshan disease (disorder)", "disease (or disorder); Keshan", "enlarged heart and poor heart function", "Selenium deficiency cardiomyopathy syndrome", "congestive cardiomyopathy due to selenium deficiency", "Congestive cardiomyopathy due to selenium deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Keshan disease", "shortest_name_length": 6}
{"curie": "MONDO:0032837", "names": ["AOMS4", "ABDOMINAL OBESITY-METABOLIC SYNDROME 4", "abdominal obesity-metabolic syndrome 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "abdominal obesity-metabolic syndrome 4", "shortest_name_length": 5}
{"curie": "MONDO:0021463", "names": ["parathyroid tumor benign", "Benign Parathyroid Tumor", "PARATHYROID TUMOR BENIGN", "benign parathyroid tumor", "Parathyroid tumor benign", "Parathyroid Tumor Benign", "Parathyroid tumour benign", "benign tumor of parathyroid", "Benign Parathyroid Neoplasm", "Benign Tumor of Parathyroid", "benign parathyroid neoplasm", "Benign Neoplasm of Parathyroid", "benign parathyroid gland tumor", "Benign Parathyroid Gland Tumor", "benign neoplasm of parathyroid", "benign tumor of the parathyroid", "Benign Tumor of the Parathyroid", "Benign Tumor of Parathyroid Gland", "Benign Parathyroid Gland Neoplasm", "Benign tumor of parathyroid gland", "benign parathyroid gland neoplasm", "benign tumor of parathyroid gland", "parathyroid gland benign neoplasm", "Benign Neoplasm of the Parathyroid", "benign neoplasm of the parathyroid", "Benign tumour of parathyroid gland", "Benign Neoplasm of Parathyroid Gland", "Benign neoplasm of parathyroid gland", "benign neoplasm of parathyroid gland", "Benign Tumor of the Parathyroid Gland", "benign tumor of the parathyroid gland", "benign neoplasm of the parathyroid gland", "Benign Neoplasm of the Parathyroid Gland", "Benign neoplasm of parathyroid gland (disorder)", "benign neoplasm of parathyroid gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of parathyroid gland", "shortest_name_length": 24}
{"curie": "MONDO:0004548", "names": ["Adult Testicular Granulosa Cell Tumor", "adult testicular granulosa cell tumor", "Adult Type Testicular Granulosa Cell Tumor", "adult type testicular granulosa cell tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult type testicular granulosa cell tumor", "shortest_name_length": 37}
{"curie": "UMLS:C5418150", "names": ["Bile Duct Intraductal Papillary Neoplasm with Intermediate Grade Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bile Duct Intraductal Papillary Neoplasm with Intermediate Grade Intraepithelial Neoplasia", "shortest_name_length": 90}
{"curie": "UMLS:C0423172", "names": ["Canaliculitis", "canaliculitis", "Canaliculitides", "lacrimal canaliculitis", "Lacrimal Canaliculitis", "Canaliculitis, Lacrimal", "Lacrimal Canaliculitides", "Canaliculitides, Lacrimal", "Lacrimal duct inflammation", "Lacrimal canaliculitis, NOS", "Lacrimal canaliculus inflamed", "lacrimal passages; inflammation", "inflammation; lacrimal passages", "Inflammation of lacrimal passage", "inflammation of lacrimal passages", "lacrimal canaliculitis (diagnosis)", "Inflammation of lacrimal canaliculus", "inflammation of lacrimal passages (diagnosis)", "Inflammation of lacrimal canaliculus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Canaliculitis", "shortest_name_length": 13}
{"curie": "UMLS:C0836973", "names": ["Acute Myelomonocytic Leukemia in Remission", "leukemia acute myelomonocytic in remission", "acute myelomonocytic leukemia in remission", "Acute myelomonocytic leukemia, in remission", "Acute myelomonocytic leukaemia, in remission", "acute myelomonocytic leukemia in remission (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute myelomonocytic leukemia, in remission", "shortest_name_length": 42}
{"curie": "UMLS:C1963747", "names": ["herpes simplex hepatitis", "Herpes simplex hepatitis", "Herpes simplex hepatitis (disorder)", "herpes simplex hepatitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Herpes simplex hepatitis", "shortest_name_length": 24}
{"curie": "MONDO:0008565", "names": ["thyroglossal duct cysts", "Thyroglossal tract cyst", "Familial thyroglossal duct cyst", "familial thyroglossal duct cyst", "thyroglossal duct cysts familial", "THYROGLOSSAL DUCT CYST, FAMILIAL", "Thyroglossal Duct Cyst, Familial", "thyroglossal duct cyst, familial", "Thyroglossal duct cysts familial", "hereditary thyroglossal duct cyst", "Hereditary thyroglossal duct cysts", "hereditary thyroglossal duct cysts", "Familial thyroglossal duct cyst (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial thyroglossal duct cyst", "shortest_name_length": 23}
{"curie": "MONDO:0008911", "names": ["cardiac lipidosis, familial", "CARDIAC LIPIDOSIS, FAMILIAL", "Cardiac Lipidosis, Familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiac lipidosis, familial", "shortest_name_length": 27}
{"curie": "UMLS:C1868833", "names": ["Bronchial wall thickening"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bronchial wall thickening", "shortest_name_length": 25}
{"curie": "UMLS:C1709660", "names": ["Primary Cutaneous T-Cell/Histiocyte Rich Lymphoma", "Primary Cutaneous T-Cell/Histiocyte-Rich Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Cutaneous T-Cell/Histiocyte-Rich Large B-Cell Lymphoma", "shortest_name_length": 49}
{"curie": "UMLS:C3665473", "names": ["Deafness both ears", "Bilateral Deafness", "Deafness bilateral", "Deafness Bilateral", "bilateral deafness", "Bilateral deafness", "deafness both ears", "Deafness Bilaterals", "Bilateral, Deafness", "Deafness, Bilateral", "Bilaterals, Deafness", "Bilateral deafness (disorder)", "deafness both ears (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bilateral Deafness", "shortest_name_length": 18}
{"curie": "UMLS:C1336209", "names": ["Stage IIIA Large Cell Lung Cancer", "Stage IIIA Large Cell Lung Carcinoma", "Stage IIIA Large Cell Carcinoma of Lung", "Stage IIIA Large Cell Carcinoma of the Lung", "Stage IIIA Lung Large Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Lung Large Cell Carcinoma AJCC v7", "shortest_name_length": 33}
{"curie": "MONDO:0009265", "names": ["GD1", "Gd 1", "GD I", "GBA Deficiency", "Gba deficiency", "Gba Deficiency", "GBA DEFICIENCY", "Deficiency, GBA", "GBA Deficiencies", "Deficiencies, GBA", "Gaucher Disease Type 1", "Gaucher disease type I", "Gaucher disease type 1", "Type 1 Gaucher Disease", "Gaucher disease, type 1", "Gaucher Disease, Type 1", "Chronic Gaucher Disease", "Gaucher disease, type I", "Gaucher Disease, Type I", "GAUCHER DISEASE, TYPE I", "Gaucher Disease, Chronic", "Disease, Chronic Gaucher", "Gaucher's disease type I", "Gaucher's disease, type I", "Glucocerebrosidase Deficiency", "GLUCOCEREBROSIDASE DEFICIENCY", "Acid Beta-Glucosidase Deficiency", "ACID BETA-GLUCOSIDASE DEFICIENCY", "acid Beta-glucosidase deficiency", "Acid beta-glucosidase deficiency", "Non Neuronopathic Gaucher Disease", "Non-Neuronopathic Gaucher Disease", "Gaucher Disease, Non-Neuronopathic", "Disease, Non-Neuronopathic Gaucher", "Glucocerebrosidase deficiency type I", "Gaucher disease, noncerebral juvenile", "Gaucher Disease, Noncerebral Juvenile", "GAUCHER DISEASE, NONCEREBRAL JUVENILE", "Non-cerebral juvenile Gaucher disease", "non-cerebral juvenile Gaucher disease", "Noncerebral juvenile Gaucher's disease", "Gaucher Disease, Non-Neuronopathic Form", "Gaucher Disease, Non Neuronopathic Form", "Gaucher's disease I, infantile or juvenile form, (non-cerebral)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gaucher disease type I", "shortest_name_length": 3}
{"curie": "UMLS:C0278837", "names": ["Prostate cancer stage IV", "stage IV prostate cancer", "cancer iv prostate stage", "Stage IV Prostate Cancer", "stage iv prostate cancer", "prostate cancer, stage IV", "Prostatic cancer stage IV", "Stage IV Prostate Carcinoma", "stage IV cancer of the prostate", "Stage IV Prostate Cancer AJCC v6", "Prostate Cancer Stage IV AJCC v6", "cancer of the prostate, stage IV", "Stage IV Prostatic Cancer AJCC v6", "stage IV carcinoma of the prostate", "Carcinoma of the prostate stage IV", "Prostate Carcinoma Stage IV AJCC v6", "Stage IV Cancer of Prostate AJCC v6", "carcinoma of the prostate, stage IV", "Cancer of Prostate Stage IV AJCC v6", "Stage IV Prostate Carcinoma AJCC v6", "Stage IV Prostatic Carcinoma AJCC v6", "Cancer of the Prostate Stage IV AJCC v6", "Stage IV Cancer of the Prostate AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Prostate Carcinoma", "shortest_name_length": 24}
{"curie": "MONDO:0004118", "names": ["Cystitis cystica", "Cystitis Cystica", "cystitis cystica", "cystitis; cystica", "cystica; cystitis", "Cystitis cystica (disorder)", "cystitis cystica (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cystitis cystica", "shortest_name_length": 16}
{"curie": "MONDO:0000921", "names": ["AMPULLAOFVATER", "ampullary tumor", "Ampullary tumor", "ampulla of Vater tumor", "Ampulla of Vater Tumor", "ampulla of vater neoplasm", "Tumor of Ampulla of Vater", "Tumor of ampulla of Vater", "tumor of ampulla of Vater", "Ampulla of Vater Neoplasm", "Tumour of ampulla of Vater", "Neoplasm of ampulla of Vater", "neoplasm of ampulla of Vater", "Neoplasm of Ampulla of Vater", "neoplasm of ampulla of vater", "tumor of the ampulla of Vater", "Tumor of the Ampulla of Vater", "hepatopancreatic ampulla tumor", "neoplasm of the ampulla of Vater", "Neoplasm of the Ampulla of Vater", "ampulla of Vater benign neoplasm", "hepatopancreatic ampulla neoplasm", "Tumor of hepatopancreatic ampulla", "tumor of hepatopancreatic ampulla", "Tumour of hepatopancreatic ampulla", "neoplasm of hepatopancreatic ampulla", "Neoplasm of ampulla of Vater (disorder)", "Neoplasm of ampulla of Vater (diagnosis)", "hepatopancreatic ampulla neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ampulla of vater neoplasm", "shortest_name_length": 14}
{"curie": "UMLS:C3900114", "names": ["Acute Humoral Allograft Nephropathy", "Acute humoral allograft nephropathy", "Acute Humoral Kidney Allograft Nephropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute humoral allograft nephropathy", "shortest_name_length": 35}
{"curie": "UMLS:C4521788", "names": ["IIB", "Stage IIB Gastric (Stomach) Cancer", "Pathologic Stage IIB Gastric Cancer AJCC v8", "Pathologic Stage IIB Gastric Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IIB Gastric Cancer AJCC v8", "shortest_name_length": 3}
{"curie": "UMLS:C5555932", "names": ["Keratin-Filled Cyst"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Keratin-Filled Cyst", "shortest_name_length": 19}
{"curie": "MONDO:0014355", "names": ["DCWHKTA", "dilated cardiomyopathy with woolly hair, keratoderma, and tooth agenesis", "CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR, KERATODERMA, AND TOOTH AGENESIS", "cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis", "shortest_name_length": 7}
{"curie": "UMLS:C0271382", "names": ["nystagmus periodic alternating", "Periodic alternating nystagmus", "Periodic Alternating Nystagmus", "Nystagmus, Periodic Alternating", "Nystagmus, periodic alternating", "Periodic alternating nystagmus (disorder)", "Periodic alternating nystagmus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Periodic Alternating Nystagmus", "shortest_name_length": 30}
{"curie": "MONDO:0011667", "names": ["MODY4", "MODY type 4", "MODY, Type 4", "MODY, type 4", "MODY, TYPE 4", "MODY, type IV", "diabetes mellitus MODY type 4", "PDX1-Associated Monogenic Diabetes", "PDX1-associated monogenic diabetes", "MODY insulin promoter factor-1 related", "maturity-onset diabetes of the young type 4", "type 4 maturity-onset diabetes of the young", "Maturity-Onset Diabetes of the Young, Type 4", "Maturity Onset Diabetes of the Young, Type 4", "MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 4", "maturity onset diabetes of the Young, type 4", "Maturity-onset diabetes of the young, type 4", "maturity-onset diabetes of the young, type 4", "maturity-onset diabetes of the young - type 4", "PDX1 maturity-onset diabetes of the young (disease)", "Maturity-onset diabetes of the young, type 4 (disorder)", "MATURITY-ONSET DIABETES OF THE YOUNG, TYPE IV (disorder)", "maturity-onset diabetes of the young - type 4 (diagnosis)", "maturity-onset diabetes of the young (disease) caused by mutation in PDX1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maturity-onset diabetes of the young type 4", "shortest_name_length": 5}
{"curie": "UMLS:C2828199", "names": ["Stage IA Bone Cancer", "Stage IA Bone Cancer AJCC v7", "Stage IA Bone Cancer  AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Bone Cancer AJCC v7", "shortest_name_length": 20}
{"curie": "UMLS:C1868821", "names": ["Immediate post-injection reaction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immediate post-injection reaction", "shortest_name_length": 33}
{"curie": "MONDO:0002561", "names": ["phospholipidosis", "lysosome disease", "PHOSPHOLIPIDOSIS", "lysosomal disease", "lysosome disorder", "lysosomal disorder", "Lysosomal enzyme defect", "defect; lysosomal enzyme", "lysosomal enzyme; defect", "Lysosomal enzyme disorder", "Lysosomal storage disease", "lysosomal storage disease", "Lysosomal Enzyme Disorder", "Lysosomal Storage Disease", "lysosomal storage diseases", "Disorder, Lysosomal Enzyme", "Lysosomal storage disorder", "Lysosomal Storage Diseases", "Enzyme Disorder, Lysosomal", "Lysosomal Storage Disorder", "Lysosomal storage diseases", "Disease, Lysosomal Storage", "lysosomal storage disorder", "Lysosomal Enzyme Disorders", "Diseases, Lysosomal Storage", "Enzyme Disorders, Lysosomal", "Disorders, Lysosomal Enzyme", "Lysosomal storage disorders", "lysosomal storage disorders", "Disorder of lysosomal enzyme", "disorder of lysosomal enzyme", "disorder of lysosomal enzymes", "Disorder of Lysosomal Enzymes", "DISORDERS OF LYSOSOMAL ENZYMES", "inborn lysosomal enzyme disorder", "Disorder of lysosomal enzyme, NOS", "Lysosomal storage disease (disorder)", "lysosomal storage metabolism disorder", "Disorder of lysosomal enzyme (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lysosomal storage disease", "shortest_name_length": 16}
{"curie": "UMLS:C4521864", "names": ["Stage IA Ampulla of Vater Cancer", "Stage IA Ampulla of Vater Cancer AJCC v8", "Stage IA Ampulla of Vater Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Ampulla of Vater Cancer AJCC v8", "shortest_name_length": 32}
{"curie": "MONDO:0004446", "names": ["olfactory groove meningioma", "Olfactory Groove Meningioma", "Meningioma, Olfactory Groove", "Olfactory Groove Meningiomas", "Groove Meningiomas, Olfactory", "Meningiomas, Olfactory Groove", "meningioma of olfactory groove", "Meningioma of Olfactory Groove", "meningioma of the olfactory groove", "Meningioma of the Olfactory Groove", "meningioma of the Olfactory Groove", "olfactory sulcus meningioma (disease)", "meningioma (disease) of olfactory sulcus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "olfactory groove meningioma", "shortest_name_length": 27}
{"curie": "UMLS:C0376297", "names": ["Cardiac Death", "Cardiac death", "cardiac death", "cardiac; death", "cardiac deaths", "Death, Cardiac", "death; cardiac"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiac Death", "shortest_name_length": 13}
{"curie": "MONDO:0007615", "names": ["MIP", "LSS", "TMIP", "Sandrow syndrome", "SANDROW SYNDROME", "LAURIN-SANDROW SYNDROME", "laurin Sandrow syndrome", "laurin-Sandrow syndrome", "Laurin-Sandrow syndrome", "Laurin Sandrow syndrome", "MIRROR-IMAGE POLYDACTYLY", "Mirror image polydactyly", "mirror-image polydactyly", "Mirror-Image Polydactyly", "Mirror-image polydactyly", "mirror-Image polydactyly", "LAURIN-SANDROW SYNDROME, SEGMENTAL", "Mirror image duplication of digits", "laurin-Sandrow syndrome, segmental", "Laurin-Sandrow Syndrome, Segmental", "Mirror-image polydactyly (disorder)", "TETRAMELIC MIRROR-IMAGE POLYDACTYLY", "tetramelic mirror-image polydactyly", "tetramelic mirror-Image polydactyly", "Tetramelic mirror-image polydactyly", "MIRROR HANDS AND FEET WITH NASAL DEFECTS", "mirror hands and feet with nasal defects", "miccor hands and feet with nasal defects", "Mirror hands and feet with nasal defects", "Fibula ulna duplication tibia radius absence", "fibula ulna duplication tibia radius absence", "mirror hands and feets-nasal defects syndrome", "Mirror hands and feets-nasal defects syndrome", "Mirror hands and feet co-occurrent with nasal defect", "Mirror hands and feet co-occurrent with nasal defect (disorder)", "MIPduplication of fibuland ulna with absence of tibia and radius", "fibula and ulna, Duplication of, with absence of tibia and radius", "Fibula And Ulna, Duplication Of, With Absence Of Tibia And Radius", "FIBULA AND ULNA, DUPLICATION OF, WITH ABSENCE OF TIBIA AND RADIUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laurin-Sandrow syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C0400918", "names": ["Chronic viral hepatitis B with hepatitis D", "Chronic viral hepatitis B with delta-agent", "chronic hepatitis, B virus with hepatitis delta", "chronic hepatitis B infection with hepatitis delta", "hepatitis; virus, chronic, type B, with delta-agent", "Chronic viral hepatitis B with hepatitis D (disorder)", "chronic viral hepatitis B infection with hepatitis delta", "chronic hepatitis B infection with hepatitis delta (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic viral hepatitis B with hepatitis D", "shortest_name_length": 42}
{"curie": "UMLS:C0393519", "names": ["early-onset cerebellar ataxia", "Early onset cerebellar ataxia", "Early-onset cerebellar ataxia", "cerebellar ataxia early-onset", "Early Onset Cerebellar Ataxia", "Cerebellar Ataxia, Early Onset", "cerebellar; ataxia, early onset", "ataxia; cerebellar, early onset", "Early onset cerebellar ataxia (disorder)", "early-onset cerebellar ataxia (diagnosis)", "Early-onset cerebellar ataxia, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebellar Ataxia, Early Onset", "shortest_name_length": 29}
{"curie": "UMLS:C1704377", "names": ["bright disease", "BRIGHT DISEASE", "Bright Disease", "bright diseases", "Bright; disease", "disease; Bright", "Brights disease", "brights disease", "bright's disease", "Bright's disease", "brights diseases", "disease bright's", "bright's diseases", "Bright's disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bright Disease", "shortest_name_length": 14}
{"curie": "UMLS:C4055494", "names": ["AML with t(5;17)(q35;q21)", "AML with t(5;17)(q35;q21);NPM1-RARA", "Acute Myeloid Leukemia with t(5;17)(q35;q21)", "Acute Myeloid Leukemia with t(5;17)(q35;q21);NPM1-RARA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Myeloid Leukemia with t(5;17)(q35;q21)", "shortest_name_length": 25}
{"curie": "MONDO:0000809", "names": ["PURPURA FULMINANS", "purpura fulminans", "fulminans purpura", "Purpura Fulminans", "Purpura fulminans", "purpura gangrenosa", "Purpura, fulminans", "purpura; fulminans", "fulminans; purpura", "Fulminans, Purpura", "Fibrinolytic purpura", "purpura fibrinolytic", "fibrinolytic purpura", "Purpura;fibrinolytic", "Purpura, fibrinolytic", "fibrinolytic; purpura", "purpura; fibrinolytic", "Purpura fulminans (disorder)", "purpura fulminans (diagnosis)", "fibrinolytic purpura (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "purpura fulminans", "shortest_name_length": 17}
{"curie": "MONDO:0015448", "names": ["isolated complex III deficiency", "mitochondrial complex III deficiency", "isolated CoQ-cytochrome C reductase deficiency", "isolated ubiquinone-cytochrome C reductase deficiency", "isolated coenzyme Q-cytochrome C reductase deficiency", "isolated mitochondrial respiratory chain complex III deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex III deficiency", "shortest_name_length": 31}
{"curie": "MONDO:0017814", "names": ["bone lymphoma", "lymphoma of bone", "Lymphoma of the bone", "lymphoma of the bone", "bone tissue lymphoma", "primary bone lymphoma", "Primary bone lymphoma", "Primary Bone Lymphoma", "lymphoma of bone tissue", "primary lymphoma of bone", "Primary Lymphoma of Bone", "primary lymphoma of the bone", "Primary Lymphoma of the Bone", "Primary bone lymphoma (disorder)", "Primary bone lymphoma (diagnosis)", "bone neoplasm malignant lymphoma primary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary bone lymphoma", "shortest_name_length": 13}
{"curie": "MONDO:0009735", "names": ["NS", "NETH", "neth", "NETHERTON DISEASE", "Netherton disease", "Netherton Disease", "NETHERTON SYNDROME", "Netherton syndrome", "netherton syndrome", "Netherton Syndrome", "nethertons syndrome", "Netherton's disease", "bamboo hair syndrome", "Bamboo hair syndrome", "Netherton's syndrome", "netherton's syndrome", "COMEL-NETHERTON SYNDROME", "Comèl-Netherton syndrome", "Comel-Netherton syndrome", "Netherton's syndrome (disorder)", "Axial osteosclerosis with bamboo hair", "lamellar ichthyosis and trichorrhexis invaginata syndrome", "Lamellar ichthyosis AND trichorrhexis invaginata syndrome", "Lamellar ichthyosis and trichorrhexis invaginata syndrome", "ERYTHRODERMA, ICHTHYOSIFORM, WITH HYPOTRICHOSIS AND HYPER-IgE", "erythroderma, ichthyosiform, with hypotrichosis and hyper-IgE", "Lamellar ichthyosis AND trichorrhexis invaginata syndrome (disorder)", "lamellar ichthyosis and trichorrhexis invaginata syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Netherton syndrome", "shortest_name_length": 2}
{"curie": "MONDO:0016952", "names": ["1q duplications", "partial trisomy 1q", "partial trisomy of chromosome 1q", "partial duplication of chromosome 1q", "partial trisomy of the long arm of chromosome 1", "partial duplication of the long arm of chromosome 1", "partial duplication of the long arm of chromosome type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of the long arm of chromosome 1", "shortest_name_length": 15}
{"curie": "MONDO:0011973", "names": ["TNZD", "ZINC IN BREAST MILK, REDUCED", "zinc in breast milk, reduced", "zinc deficiency, transient neonatal", "ZINC DEFICIENCY, TRANSIENT NEONATAL", "Zinc Deficiency, Neonatal, due to Low Breast Milk Zinc", "zinc deficiency, neonatal, due to Low breast milk zinc", "ZINC DEFICIENCY, NEONATAL, DUE TO LOW BREAST MILK ZINC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "zinc deficiency, transient neonatal", "shortest_name_length": 4}
{"curie": "MONDO:0014855", "names": ["MRD42", "autosomal dominant mental retardation 42", "mental retardation, autosomal dominant 42", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 42", "autosomal dominant intellectual disability 42", "mental retardation, autosomal dominant type 42", "intellectual disability, autosomal dominant 42", "intellectual disability, autosomal dominant type 42", "autosomal dominant intellectual developmental disorder 42", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 42", "intellectual developmental disorder, autosomal dominant 42", "autosomal dominant non-syndromic intellectual disability 42", "Gnb1 autosomal dominant non-syndromic intellectual disability", "GNB1 autosomal dominant non-syndromic intellectual disability", "autosomal dominant non-syndromic intellectual disability caused by mutation in GNB1", "autosomal dominant non-syndromic intellectual disability caused by mutation in Gnb1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 42", "shortest_name_length": 5}
{"curie": "UMLS:C4289313", "names": ["FIGO Stage IIIA2 Ovarian Cancer", "FIGO Stage IIIA2 Ovarian Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Stage IIIA2 Ovarian Cancer", "shortest_name_length": 31}
{"curie": "MONDO:0020132", "names": ["cranial nerve and nuclear aplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cranial nerve and nuclear aplasia", "shortest_name_length": 33}
{"curie": "UMLS:C4055116", "names": ["Drug and toxin-induced pulmonary arterial hypertension", "Drug- and Toxin-Induced Pulmonary Arterial Hypertension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drug and toxin-induced pulmonary arterial hypertension", "shortest_name_length": 54}
{"curie": "MONDO:0007864", "names": ["KTS", "KTW Syndrome", "KTW SYNDROME", "Ktw syndrome", "Syndrome, KTW", "KTW Syndromes", "weber syndrome", "Syndromes, KTW", "Weber syndrome", "syndrome webers", "webers syndrome", "Klippel-Trenaunay", "phlebarteriectasis", "Parkes Weber syndrome", "parkes weber syndrome", "osteo-angiohypertrophy", "Weber-Klippel-Trenaunay", "Klippel Trenaunay Disease", "nevus osteohypertrophicus", "Klippel-Trenaunay Disease", "Klippel-Trenaunay Syndrome", "Cerebrofacial angiomatosis", "Klippel Trenaunay Syndrome", "Disease, Klippel-Trenaunay", "KLIPPEL-TRENAUNAY SYNDROME", "Klippel-Trénaunay syndrome", "Klippel Trenaunay syndrome", "klippel-trenaunay syndrome", "Klippel-Trenaunay syndrome", "Syndrome, Klippel Trenaunay", "Syndrome, Klippel-Trenaunay", "haemangiectatic hypertrophy", "Haemangiectatic hypertrophy", "Klippel-Trenaunay Syndromes", "Syndromes, Klippel-Trenaunay", "hemangiectasia hypertrophica", "ANGIOOSTEOHYPERTROPHY SYNDROME", "Angioosteohypertrophy Syndrome", "angioosteohypertrophy syndrome", "Syndrome, Angioosteohypertrophy", "angioosteohypertrophic syndrome", "Angio-Osteohypertrophy Syndrome", "Angio Osteohypertrophy Syndrome", "angio-osteohypertrophy syndrome", "Angioosteohypertrophic syndrome", "Angioosteohypertrophy Syndromes", "Klippel-Trénaunay-Weber syndrome", "KLIPPEL-TRENAUNAY-WEBER SYNDROME", "klippel syndrome trenaunay weber", "Congenital Dysplastic Angiopathy", "Klippel-Trenaunay syndrome (KTS)", "Klippel-Trenaunay-Weber Syndrome", "klippel trenaunay weber syndrome", "Angio-osteohypertrophic syndrome", "klippel weber trenaunay syndrome", "Klippel Trénaunay Weber Syndrome", "Syndromes, Angioosteohypertrophy", "Klippel-Trenaunay-Weber syndrome", "Syndrome, Angio-Osteohypertrophy", "syndrome klippel-trenaunay-weber", "Angio-Osteohypertrophy Syndromes", "Klippel-Trénaunay-Weber Syndrome", "Klippel Trenaunay Weber Syndrome", "klippel-trenaunay-weber syndrome", "Syndrome, Klippel-Trenaunay-Weber", "Angiopathy, Congenital Dysplastic", "Dysplastic Angiopathy, Congenital", "Syndrome, Klippel-Trénaunay-Weber", "Syndromes, Angio-Osteohypertrophy", "Congenital Dysplastic Angiopathies", "Angiopathies, Congenital Dysplastic", "Dysplastic Angiopathies, Congenital", "osteohypertrophic varicose syndrome", "nevus varicosus osteohypertrophicus", "Klippel Trenaunay syndrome (disorder)", "naevus vasculosus osteohypertrophicus", "Klippel-Trenaunay-Weber (KTW) syndrome", "Ollier-Klippel-Trenaunay-Weber syndrome", "Klippel-Treneunay-Parkes Weber syndrome", "hemangiectatic hypertrophy of Parkes Weber", "Angio-osteohypertrophic syndrome (disorder)", "Klippel-Trenaunay-Weber syndrome (diagnosis)", "Klippel-Trenaunay-Weber syndrome, Isolated cases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angioosteohypertrophic syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0011150", "names": ["PENTT", "PENTTINEN SYNDROME", "Penttinen-Aula syndrome", "Penttinen-aula syndrome", "progeroid syndrome, Penttinen type", "Premature aging syndrome Penttinen type", "premature aging syndrome Penttinen type", "Premature ageing syndrome Penttinen type", "Premature Aging Syndrome, Penttinen Type", "premature aging syndrome, Penttinen type", "Premature aging syndrome, Penttinen type", "PREMATURE AGING SYNDROME, PENTTINEN TYPE", "Acroosteolysis-keloid-like lesions-premature aging syndrome", "acroosteolysis-keloid-like lesions-premature aging syndrome", "Acroosteolysis, keloid-like lesions, premature aging syndrome", "Acroosteolysis, keloid-like lesions, premature ageing syndrome", "Acroosteolysis, keloid-like lesions, premature aging syndrome (disorder)", "prematurely aged appearance, delayed bone maturation, acro-osteolysis, and brachydactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acroosteolysis-keloid-like lesions-premature aging syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0334335", "names": ["Adrenal Gland Glomerulosa Cell Adenoma", "Adrenal Cortex Glomerulosa Cell Adenoma", "Glomerulosa Cell Adrenocortical Adenoma", "Glomerulosa Cell Adrenal Cortex Adenoma", "Adrenal Cortical Glomerulosa Cell Adenoma", "Glomerulosa Cell Adrenal Cortical Adenoma", "Adrenal cortical adenoma, glomerulosa cell", "adenoma; glomerulosa cell, adrenal (cortex)", "Adrenal cortical adenoma - glomerulosa cell", "glomerulosa cell; adenoma, adrenal (cortex)", "Adrenal cortical adenoma, glomerulosa cell type", "Adrenal cortical adenoma, glomerulosa cell (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Glomerulosa Cell Adrenal Cortical Adenoma", "shortest_name_length": 38}
{"curie": "MONDO:0001964", "names": ["Chronic tubotympanic suppurative otitis media", "chronic tubotympanic suppurative otitis media", "Chronic suppurative otitis media - tubotympanic", "otitis; media, chronic, suppurative, tubotympanic", "Chronic tubotympanic suppurative otitis media (disorder)", "chronic tubotympanic suppurative otitis media (diagnosis)", "Chronic tubotympanic suppurative otitis media, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic tubotympanic suppurative otitis media", "shortest_name_length": 45}
{"curie": "UMLS:C5669676", "names": ["Multiple Solitary Plasmacytoma of Bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Multiple Solitary Plasmacytoma of Bone", "shortest_name_length": 38}
{"curie": "UMLS:C5239342", "names": ["Recurrent Soft Tissue Sarcoma of the Trunk and Extremities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Soft Tissue Sarcoma of the Trunk and Extremities", "shortest_name_length": 58}
{"curie": "MONDO:0002577", "names": ["bile duct rhabdomyosarcoma", "rhabdomyosarcoma of the bile duct", "bile duct rhabdomyosarcoma (disease)", "Extrahepatic Bile Duct Rhabdomyosarcoma", "extrahepatic bile duct rhabdomyosarcoma", "rhabdomyosarcoma of extrahepatic bile duct", "Rhabdomyosarcoma of Extrahepatic Bile Duct", "rhabdomyosarcoma of the extrahepatic bile duct", "Rhabdomyosarcoma of the Extrahepatic Bile Duct", "extrahepatic bile duct rhabdomyosarcoma (disease)", "rhabdomyosarcoma (disease) of extrahepatic bile duct", "rhabdomyosarcoma of extrahepatic bile duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extrahepatic bile duct rhabdomyosarcoma", "shortest_name_length": 26}
{"curie": "UMLS:C3888024", "names": ["cacosmia", "Dysosmia", "Cacosmia", "Cacosmias", "Dysosmias"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cacosmia", "shortest_name_length": 8}
{"curie": "UMLS:C1710673", "names": ["Widely Invasive Thymoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Widely Invasive Thymoma", "shortest_name_length": 23}
{"curie": "UMLS:C5420542", "names": ["Locally Advanced Endometrioid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Endometrioid Adenocarcinoma", "shortest_name_length": 44}
{"curie": "MONDO:0021042", "names": ["GLIOMA", "glioma", "Glioma", "GLIOMAS", "gliomas", "Gliomas", "Glial Tumor", "glial tumor", "Glial tumor", "Glioma, NOS", "glial tumors", "Glial Neoplasm", "glial neoplasm", "glial cell tumor", "Glial Cell Tumor", "Neuroglial Tumor", "neuroglial tumor", "Glial Cell Tumors", "Glioma (disorder)", "Tumor, Glial Cell", "Tumor of Neuroglia", "Tumors, Glial Cell", "glioma (diagnosis)", "tumor of neuroglia", "Neuroglial Neoplasm", "neuroglial neoplasm", "neoplasm of neuroglia", "Neoplasm of Neuroglia", "tumor of the neuroglia", "Tumor of the Neuroglia", "glioma; unspecified site", "Neoplasm of the Neuroglia", "neoplasm of the neuroglia", "Glioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glioma", "shortest_name_length": 6}
{"curie": "MONDO:0012273", "names": ["DFNB48", "autosomal recessive deafness 48", "deafness, autosomal recessive 48", "DEAFNESS, AUTOSOMAL RECESSIVE 48", "Deafness, Autosomal Recessive 48", "deafness, autosomal recessive type 48", "autosomal recessive nonsyndromic deafness 48", "CIB2 autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 48", "autosomal recessive nonsyndromic deafness type 48", "autosomal recessive nonsyndromic deafness caused by mutation in CIB2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 48", "shortest_name_length": 6}
{"curie": "MONDO:0054742", "names": ["COXPD35", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 35", "combined oxidative phosphorylation deficiency 35"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation deficiency 35", "shortest_name_length": 7}
{"curie": "MONDO:0014001", "names": ["USH1K", "Usher syndrome type 1K", "Usher syndrome type IK", "USHER SYNDROME, TYPE IK", "USHER syndrome, type IK"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Usher syndrome type 1K", "shortest_name_length": 5}
{"curie": "UMLS:C0948226", "names": ["spasm; ureter", "ureter; spasm", "Ureteral spasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ureteral spasm", "shortest_name_length": 13}
{"curie": "UMLS:C0340858", "names": ["drug; hypotension", "Hypotension due to drug", "Hypotension due to Drug", "hypotension drug-induced", "Hypotension due to drugs", "Drug-induced hypotension", "hypotension; due to drugs", "Drug-induced hypotension (disorder)", "Drug-induced hypotension (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drug-induced hypotension", "shortest_name_length": 17}
{"curie": "UMLS:C2931909", "names": ["Hyperlipidema, Familial", "Hyperlipoproteinemia, type 2 A", "High serum cholesterol, familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High serum cholesterol, familial", "shortest_name_length": 23}
{"curie": "UMLS:C4331499", "names": ["Ventricular and Brain Stem Ependymal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ventricular and Brain Stem Ependymal Tumor", "shortest_name_length": 42}
{"curie": "MONDO:0020806", "names": ["SA BLOCK", "sa block", "SA block", "sinoatrial block", "Sinoatrial Block", "Sinoatrial block", "SINOATRIAL BLOCK", "Sinoatrial Blocks", "Block, Sinoatrial", "sinoatrial; block", "block; sinoatrial", "Blocks, Sinoatrial", "Sinoauricular block", "block; sinoauricular", "sinoauricular; block", "Sinoatrial block, NOS", "Sinoatrial exit block", "Sinoatrial Exit Block", "Heart block sinoatrial", "Sinoatrial Exit Blocks", "Block, Sinoatrial Exit", "Exit Block, Sinoatrial", "sinoatrial heart block", "Blocks, Sinoatrial Exit", "Exit Blocks, Sinoatrial", "Sinoauricular block, NOS", "HEART BLOCK SINOAURICULAR", "Heart block sinoauricular", "Sinoatrial block (disorder)", "sinoatrial block (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sinoatrial block", "shortest_name_length": 8}
{"curie": "MONDO:0014449", "names": ["ANALBA", "analbuminemia", "ANALBUMINEMIA", "Analbuminemia", "Analbuminaemia", "analbuminaemia", "Analbuminemia (finding)", "Congenital analbuminemia", "congenital analbuminemia", "analbuminemia (diagnosis)", "Congenital analbuminaemia", "Congenital analbuminemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital analbuminemia", "shortest_name_length": 6}
{"curie": "UMLS:C0750918", "names": ["Commisural Aphasia", "Commisural Aphasias", "Aphasia, Commisural", "Aphasias, Commisural"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aphasia, Commisural", "shortest_name_length": 18}
{"curie": "MONDO:0009866", "names": ["PCKDC", "PEPCK1 deficiency", "PEPCK 1 deficiency", "PCK1 deficiency, cytosolic", "PCK1 DEFICIENCY, CYTOSOLIC", "PEPCK deficiency, cytosolic", "PEPCK DEFICIENCY, CYTOSOLIC", "PEP carboxykinase deficiency", "phosphopyruvate carboxylase deficiency", "phosphoenolpyruvate carboxylase deficiency", "phosphoenolpyruvate carboxykinase deficiency", "phosphoenolpyruvate carboxykinase-1 (PCK1) deficiency", "Cytosolic phosphoenolpyruvate carboxykinase deficiency", "PHOSPHOENOLPYRUVATE CARBOXYKINASE DEFICIENCY, CYTOSOLIC", "phosphoenolpyruvate carboxykinase deficiency, cytosolic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phosphoenolpyruvate carboxykinase deficiency, cytosolic", "shortest_name_length": 5}
{"curie": "MONDO:0014796", "names": ["PARK23", "Parkinson's disease 23", "VPS13C young-onset Parkinson disease", "autosomal recessive early-onset Parkinson disease 23", "PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET", "Parkinson disease 23, autosomal recessive early-onset", "Parkinson disease 23, autosomal recessive, early onset", "autosomal recessive early-onset Parkinson's disease 23", "young-onset Parkinson disease caused by mutation in VPS13C", "autosomal recessive early-onset Parksinson disease type 23"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive early-onset Parkinson disease 23", "shortest_name_length": 6}
{"curie": "MONDO:0021131", "names": ["Frontal Lobe Ependymal Tumor", "frontal lobe ependymal tumor", "ependymal tumor of frontal lobe"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontal lobe ependymal tumor", "shortest_name_length": 28}
{"curie": "UMLS:C1333869", "names": ["PanIN-1", "Pancreatic Intraepithelial Neoplasia-1", "Grade I Pancreatic Intraepithelial Neoplasia", "Grade 1 Pancreatic Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Intraepithelial Neoplasia-1", "shortest_name_length": 7}
{"curie": "UMLS:C5447846", "names": ["Epithelioid Hemangioendothelioma with WWTR1-CAMTA1 Gene Fusion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epithelioid Hemangioendothelioma with WWTR1-CAMTA1 Gene Fusion", "shortest_name_length": 62}
{"curie": "UMLS:C1335680", "names": ["Rectal Juvenile Polyp", "Rectal Retention Polyp", "Juvenile Polyp of Rectum", "Juvenile Polyp of the Rectum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rectal Juvenile Polyp", "shortest_name_length": 21}
{"curie": "UMLS:C1336343", "names": ["Stage IVA Larynx Epidermoid Carcinoma", "Stage IVA Larynx Squamous Cell Carcinoma", "Stage IVA Epidermoid Carcinoma of Larynx", "Stage IVA Laryngeal Epidermoid Carcinoma", "Stage IVA Squamous Cell Carcinoma of Larynx", "Stage IVA Laryngeal Squamous Cell Carcinoma", "Stage IVA Epidermoid Carcinoma of the Larynx", "Stage IVA Laryngeal Throat Squamous Cell Cancer", "Stage IVA Squamous Cell Carcinoma of the Larynx", "Stage IVA Laryngeal Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Laryngeal Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 37}
{"curie": "UMLS:C0406556", "names": ["Weary syndrome", "Hereditary acrokeratotic poikiloderma", "Hereditary acrokeratotic poikiloderma of Weary", "Hereditary acrokeratotic poikiloderma of Weary (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hereditary acrokeratotic poikiloderma of Weary", "shortest_name_length": 14}
{"curie": "MONDO:0024611", "names": ["orbit tumor", "Orbit Tumor", "orbit tumors", "Orbital Tumor", "orbital tumor", "orbit neoplasm", "Tumor of orbit", "Orbit Neoplasm", "tumor of orbit", "Tumor of Orbit", "Tumour of orbit", "orbital neoplasm", "Orbital Neoplasm", "neoplasm of orbit", "Neoplasm, Orbital", "Neoplasm of orbit", "Neoplasm of Orbit", "Orbital Neoplasms", "Orbital neoplasia", "orbital neoplasms", "tumor of the orbit", "Tumor of the Orbit", "Neoplasms, Orbital", "orbit of skull tumor", "Neoplasm of the Orbit", "neoplasm of the orbit", "Neoplasm of orbit NOS", "neoplasm of eye orbit", "tumor of orbit of skull", "orbit of skull neoplasm", "Neoplasm of orbit proper", "neoplasm of orbit of skull", "neoplasm of eye orbit (diagnosis)", "Neoplasm of orbit proper (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orbit neoplasm", "shortest_name_length": 11}
{"curie": "MONDO:0008822", "names": ["ARCS", "ARCS1", "ARC syndrome", "Arc syndrome", "Arthrogryposis, Renal Dysfunction, And Cholestasis", "arthrogryposis, renal dysfunction, and cholestasis 1", "ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1", "Arthrogryposis, renal dysfunction, and cholestasis 1", "Arthrogryposis renal dysfunction cholestasis syndrome", "arthrogryposis, renal dysfunction, and cholestasis type 1", "VPS33B arthrogryposis-renal dysfunction-cholestasis syndrome", "Arthrogryposis multiplex congenita, renal dysfunction, and cholestasis", "arthrogryposis-renal dysfunction-cholestasis syndrome caused by mutation in VPS33B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis, renal dysfunction, and cholestasis 1", "shortest_name_length": 4}
{"curie": "UMLS:C1511285", "names": ["Atypical Breast Myoepitheliosis", "Breast Atypical Myoepitheliosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Atypical Myoepitheliosis", "shortest_name_length": 31}
{"curie": "MONDO:0005824", "names": ["Legionella", "legionnaire disease", "Legionnaire Disease", "LEGIONNAIRE DISEASE", "Legionnaires disease", "Legionella Pneumonia", "Disease;Legionnaires", "legionnaires disease", "Legionnaires Disease", "Pneumonia legionella", "Disease, Legionnaire", "LEGIONELLA PNEUMONIA", "Legionella pneumonia", "pneumonia legionella", "legionella pneumonia", "disease legionnaire's", "Legionnaires' Disease", "Legionnaire's Disease", "diseases legionnaires", "Legionnaire's disease", "Legionnaires' disease", "legionnaires' disease", "legionnaire's disease", "Legionellal pneumonia", "disease legionnaires's", "legionnaire's; disease", "diseases legionnaire's", "Disease, Legionnaires'", "Legionella pneumonia, NOS", "Legionella pneumonia (disorder)", "Legionella pneumophila Infection", "Legionella pneumophila infection", "Legionella pneumophila; infection", "infection; Legionella pneumophila", "Legionnaire's disease (diagnosis)", "Legionella pneumophila Infections", "Infection, Legionella pneumophila", "Infections, Legionella pneumophila", "Infection by Legionella pneumophilia", "disease (or disorder); legionnaire's", "infection by Legionella pneumophilia", "Pneumonia due to Legionnaires' disease", "Infection caused by Legionella pneumophilia", "Infection caused by Legionella pneumophilia (disorder)", "Legionella pneumophila; infection, pneumonia (manifestation)", "infection; Legionella pneumophila, pneumonia (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Legionnaires' disease", "shortest_name_length": 10}
{"curie": "UMLS:C1336144", "names": ["Stage IB Small Cell Lung Cancer", "Stage IB Small Cell Lung Carcinoma", "Stage IB Small Cell Carcinoma of Lung", "Stage IB Small Cell Carcinoma of the Lung", "Stage IB Lung Small Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Lung Small Cell Carcinoma AJCC v7", "shortest_name_length": 31}
{"curie": "MONDO:0004871", "names": ["Perianal hematoma", "perianal hematoma", "Haematoma;perianal", "perianal haematoma", "Perianal haematoma", "hematomas perianal", "Thrombosed external pile", "external thrombosed piles", "Thrombosed piles external", "Piles;thrombosed external", "Thrombosed external hemorrhoid", "thrombosed external hemorrhoid", "external hemorrhoid thrombosed", "external thrombosed hemorrhoid", "external hemorrhoids thrombosed", "Thrombosed external hemorrhoids", "External thrombosed hemorrhoids", "thrombosed external hemorrhoids", "hemorrhoids external thrombosed", "Thrombosed external haemorrhoid", "external thrombosed hemorrhoids", "Thrombosed external haemorrhoids", "external thrombosed haemorrhoids", "External thrombosed haemorrhoids", "hemorrhoids; external, thrombosed", "hemorrhoids; thrombosed, external", "thrombosis of external hemorrhoids", "External hemorrhoids with thrombosis", "Thrombosed external hemorrhoids (disorder)", "thrombosed external hemorrhoids (diagnosis)", "thrombosis of external hemorrhoids (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "perianal hematoma", "shortest_name_length": 17}
{"curie": "UMLS:C4682557", "names": ["Stage IB Uterine Corpus Leiomyosarcoma", "Stage IB Uterine Corpus Leiomyosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Uterine Corpus Leiomyosarcoma AJCC v8", "shortest_name_length": 38}
{"curie": "UMLS:C2212013", "names": ["Serous adenocarcinofibroma", "Ovarian Serous Adenocarcinofibroma", "serous adenocarcinofibroma of ovary", "serous adenocarcinofibroma of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "serous adenocarcinofibroma of ovary", "shortest_name_length": 26}
{"curie": "MONDO:0006050", "names": ["anaplastic breast carcinoma", "Anaplastic Breast Carcinoma", "pleomorphic breast carcinoma", "Breast Pleomorphic Carcinoma", "Pleomorphic Breast Carcinoma", "anaplastic carcinoma of breast", "pleomorphic carcinoma of breast", "anaplastic carcinoma of breast (diagnosis)", "pleomorphic carcinoma of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pleomorphic breast carcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0007412", "names": ["BSTVS", "Beare-Stevenson syndrome", "Beare Stevenson syndrome", "BEARE-STEVENSON SYNDROME", "Beare-Stevenson Cutis Gyrata Syndrome", "BEARE-STEVENSON CUTIS GYRATA SYNDROME", "Beare-Stevenson cutis gyrata syndrome", "Cutis Gyrata Syndrome of Beare-Stevenson", "CUTIS GYRATA SYNDROME OF BEARE AND STEVENSON", "Cutis Gyrata Syndrome of Beare And Stevenson", "Cutis gyrata syndrome of Beare and Stevenson", "cutis gyrata syndrome of Beare and Stevenson", "cutis gyrata - acanthosis nigricans - craniosynostosis", "Cutis gyrata syndrome of Beare and Stevenson (disorder)", "cutis gyrata-acanthosis nigricans-craniosynostosis syndrome", "Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome", "Cutis gyrata, acanthosis nigricans, craniosynostosis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Beare-Stevenson cutis gyrata syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0032577", "names": ["RP83", "retinitis pigmentosa 83", "RETINITIS PIGMENTOSA 83"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 83", "shortest_name_length": 4}
{"curie": "MONDO:0009386", "names": ["HYPERLEXIA", "Hyperlexia", "hyperlexia", "Precocious reading", "precocious reading", "compulsive reading", "PRECOCIOUS READING", "Compulsive Reading", "Precocious Reading", "COMPULSIVE READING"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperlexia", "shortest_name_length": 10}
{"curie": "MONDO:0009444", "names": ["Jagell Holmgren Hofer syndrome", "Jagell-Holmgren-Hofer syndrome", "Jagell, Holmgren, Hofer syndrome", "ichthyosis alopecia eclabion ectropion mental retardation", "Ichthyosis alopecia eclabion ectropion mental retardation", "ichthyosis alopecia eclabion ectropion intellectual disability", "Ichthyosis With Alopecia, Eclabion, Ectropion, And Mental Retardation", "ICHTHYOSIS WITH ALOPECIA, ECLABIUM, ECTROPION, AND MENTAL RETARDATION", "ichthyosis with alopecia, eclabium, ectropion, and mental retardation", "ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome", "Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome", "ichthyosis with alopecia, eclabium, ectropion, and intellectual disability", "ichthyosis, alopecia, eclabion, ectropion, intellectual disability syndrome", "Ichthyosis, alopecia, eclabion, ectropion, intellectual disability syndrome", "Ichthyosis, alopecia, eclabion, ectropion, intellectual disability syndrome (disorder)", "ichthyosis, alopecia, eclabion, ectropion, intellectual disability syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome", "shortest_name_length": 30}
{"curie": "MONDO:0019978", "names": ["fetal face", "ROBINOW DWARFISM", "Robinow Syndrome", "robinow dwarfism", "Robinow Dwarfism", "Robinow dwarfism", "Robinow syndrome", "robinow syndrome", "Robinow's syndrome", "robinow's syndrome", "Fetal face syndrome", "FETAL FACE SYNDROME", "fetal face syndrome", "Fetal Face Syndrome", "Foetal face syndrome", "fetal facies syndrome", "Robinow syndrome (disorder)", "Covesdem syndrome (formerly)", "Robinow-Silverman-Smith syndrome", "Robinow-Silverman-Smith Syndrome", "Mesomelic dwarfism-small genitalia syndrome", "mesomelic dwarfism-small genitalia syndrome", "Mesomelic Dwarfism-Small Genitalia Syndrome", "acral dysostosis with facial and genital abnormalities", "Acral Dysostosis with Facial and Genital Abnormalities", "ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES", "Acral dysostosis with facial and genital abnormalities", "costovertebral segmentation defect with mesomelia (formerly)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Robinow syndrome", "shortest_name_length": 10}
{"curie": "UMLS:C2347750", "names": ["Grade II Meningioma", "grade II meningioma", "Adult Grade 2 Meningioma", "adult grade II meningioma", "Adult Grade II Meningioma", "grade II meningioma, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Grade II Meningioma", "shortest_name_length": 19}
{"curie": "MONDO:0013783", "names": ["MCOPCB7", "MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 7", "microphthalmia, isolated, with coloboma 7", "ABCB6 microphthalmia, isolated, with coloboma", "microphthalmia, isolated, with coloboma type 7", "microphthalmia, isolated, with coloboma caused by mutation in ABCB6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microphthalmia, isolated, with coloboma 7", "shortest_name_length": 7}
{"curie": "MONDO:0009028", "names": ["Crane-Heise syndrome", "CRANE-HEISE SYNDROME", "Crane Heise syndrome", "Crane Heise syndrome (disorder)", "cleft Lip/palate, agenesis of clavicles and cervical vertebrae, and talipes equinovarus", "CLEFT LIP/PALATE, AGENESIS OF CLAVICLES AND CERVICAL VERTEBRAE, AND TALIPES EQUINOVARUS", "Cleft lip-palate, agenesis of clavicles and cervical vertebrae, and talipes equinovarus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Crane-Heise syndrome", "shortest_name_length": 20}
{"curie": "MONDO:0044873", "names": ["Childhood MDS", "childhood MDS", "myelodysplastic syndrome", "Myelodysplastic Syndrome", "Childhood Myelodysplastic Syndrome", "childhood myelodysplastic syndrome", "Childhood myelodysplastic syndrome", "myelodysplastic syndrome childhood", "childhood myelodysplastic syndromes", "Childhood myelodysplastic syndrome (disorder)", "Childhood myelodysplastic syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood myelodysplastic syndrome", "shortest_name_length": 13}
{"curie": "UMLS:C4290008", "names": ["Abdominal Inflammatory Myofibroblastic Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abdominal Inflammatory Myofibroblastic Tumor", "shortest_name_length": 44}
{"curie": "UMLS:C0677658", "names": ["Disease;breast;F", "Disorder;breast;F", "female breast disease", "BREAST DISORDER FEMALE", "Breast disorder female", "Female breast disorders", "female breast disorders", "breast disorder (female)", "female breast disorders (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Female breast disorders", "shortest_name_length": 16}
{"curie": "MONDO:0040679", "names": ["urothelial carcinoma", "Urothelial carcinoma", "Urothelial Carcinoma", "Uroepithelial Carcinoma", "Uroepithelial carcinoma", "Urothelial carcinoma, NOS", "Transitional cell car. -uroth.", "transitional cell car. -uroth.", "Conventional Urothelial Carcinoma", "transitional cell carcinoma of urinary tract", "Transitional Cell Carcinoma of the Urinary Tract", "transitional cell carcinoma of the urinary tract", "transitional cell carcinoma of the urothelial tract", "Transitional cell carcinoma of the urothelial tract", "transitional cell carcinoma of urinary tract (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urothelial carcinoma", "shortest_name_length": 20}
{"curie": "MONDO:0003397", "names": ["Gum enlargement", "GUM HYPERTROPHY", "Gum hypertrophy", "gum; hypertrophy", "hypertrophy; gum", "gums hypertrophied", "Hypertrophy of gums", "HYPERTROPHY GINGIVAL", "Hypertrophy gingival", "gingival hypertrophy", "Gingival hypertrophy", "Gingival Hypertrophy", "Gingiva hypertrophia", "Gingival enlargement", "GINGIVAL HYPERTROPHY", "GINGIVA HYPERTROPHIA", "Hypertrophy, Gingival", "Hypertrophy of gingiva", "hypertrophy of gingiva", "Gingival Hypertrophies", "hypertrophy of gingivae", "Hypertrophy of gingivae", "Hypertrophic gingivitis", "Hypertrophies, Gingival", "Gingival hypertrophy, NOS", "hypertrophy; mucous membrane gum", "gum; hypertrophy mucous membrane", "mucous membrane; hypertrophy gum", "Hypertrophy of gingiva (disorder)", "gum; mucous membrane, hypertrophy", "mucous membrane; gum, hypertrophy", "hypertrophy of gingiva (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gingival hypertrophy", "shortest_name_length": 15}
{"curie": "UMLS:C4725799", "names": ["Unresectable Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Urothelial Carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0018896", "names": ["TTP", "ttp", "Moschcowitz", "T.T.P. syndrome", "Moschowitz Disease", "Moschowitz disease", "Moschcowitz Disease", "Moschkowitz Disease", "Moschcowitz disease", "MOSCHCOWITZ SYNDROME", "Moschcowitz syndrome", "Moschowitz's syndrome", "moschcowitz's syndrome", "Moschcowitz's syndrome", "PURPURA, THROMBOHEMOLYTIC", "PURPURA THROMBOPENIC THROMBOTIC", "Thrombotic Thrombopenic Purpura", "thrombotic thrombopenic purpura", "Purpura thrombopenic thrombotic", "Purpura thrombopaenic thrombotic", "Purpura, Thrombotic Thrombopenic", "Thrombopenic Purpura, Thrombotic", "thrombotic thrombocytopenic purpura", "Thrombotic-thrombocytopenic purpura", "THROMBOTIC THROMBOCYTOPENIC PURPURA", "Thrombotic thrombocytopenic purpura", "Thrombotic Thrombocytopenic Purpura", "Thrombocytopenic purpura, thrombotic", "thrombotic thrombocytopenic; purpura", "purpura; thrombotic thrombocytopenic", "Thrombocytopenic Purpura, Thrombotic", "Purpura, Thrombotic Thrombocytopenic", "purpura; thrombocytopenic, thrombotic", "PURPURA, THROMBOCYTOPENIC, THROMBOTIC", "thrombocytopenic; purpura, thrombotic", "TTP (thrombotic thrombocytopenic purpura)", "thrombotic thrombocytopenic purpura (TTP)", "TTP - Thrombotic thrombocytopenic purpura", "Thrombotic thrombocytopenic purpura (disorder)", "thrombotic thrombocytopenic purpura (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombotic thrombocytopenic purpura", "shortest_name_length": 3}
{"curie": "UMLS:C4054709", "names": ["Intermediate Bone Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intermediate Bone Neoplasm", "shortest_name_length": 26}
{"curie": "MONDO:0035742", "names": ["FV short isoforms-related bleeding disorder", "factor V short isoforms-related bleeding disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "factor V short isoforms-related bleeding disorder", "shortest_name_length": 43}
{"curie": "OMIM:611862", "names": ["WBCQ1", "WHITE BLOOD CELL COUNT QUANTITATIVE TRAIT LOCUS 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 5}
{"curie": "MONDO:0100381", "names": ["AML, t(6;11)(q27;q23)", "AML, t(6;11)(q27;q23.3)", "acute myeloid leukemia, t(6;11)(q27;q23)", "Acute Myeloid Leukemia with t(6;11)(q27;q23); MLLT4-MLL", "Acute Myeloid Leukemia with t(6;11)(q27;q23); MLL-MLLT4", "Acute Myeloid Leukemia with t(6;11)(q27;q23); KMT2A-MLLT4", "Acute Myeloid Leukemia (AML) with t(6;11)(q27;q23); KMT2A-MLLT4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, t(6;11)(q27;q23)", "shortest_name_length": 21}
{"curie": "UMLS:C4683662", "names": ["Lymphoplasmacytic Lymphoma by Ann Arbor Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoplasmacytic Lymphoma by Ann Arbor Stage", "shortest_name_length": 45}
{"curie": "MONDO:0015420", "names": ["Cleft lip & alveolus", "cleft lip and alveolus", "Cleft lip and alveolus", "Cleft lip and alveolus (diagnosis)", "Cleft lip and cleft of alveolar process of maxilla", "Cleft lip and cleft of alveolar process of maxilla (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleft lip and alveolus", "shortest_name_length": 20}
{"curie": "UMLS:C0156275", "names": ["Spontaneous Bladder Rupture", "Spontaneous rupture of bladder", "Spontaneous Bladder Perforation", "Nontraumatic rupture of bladder", "nontraumatic rupture of bladder", "Rupture of bladder, nontraumatic", "Rupture of bladder, non-traumatic", "Spontaneous rupture of bladder (disorder)", "Bladder rupture due to non-traumatic cause", "nontraumatic rupture of bladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nontraumatic rupture of bladder", "shortest_name_length": 27}
{"curie": "UMLS:C4288406", "names": ["Peripheral T-Cell Lymphoma, Unclassifiable"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peripheral T-Cell Lymphoma, Unclassifiable", "shortest_name_length": 42}
{"curie": "UMLS:C3897061", "names": ["Congenital Growth Hormone Deficiency", "Congenital growth hormone deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital growth hormone deficiency", "shortest_name_length": 36}
{"curie": "MONDO:0002474", "names": ["oxaluria", "Oxaluria", "Hyperoxaluria", "hyperoxaluria", "Primary Oxaluria", "Primary oxalosis", "Oxalosis, primary", "Primary Oxalurias", "Oxaluria, Primary", "Oxalurias, Primary", "Congenital oxaluria", "Primary Hyperoxaluria", "Primary hyperoxaluria", "primary hyperoxaluria", "PRIMARY HYPEROXALURIA", "Primary oxalosis, NOS", "hyperoxaluria primary", "hyperoxaluria, primary", "Hyperoxaluria, Primary", "Primary Hyperoxalurias", "Hyperoxalurias, Primary", "Hyperoxaluria (disorder)", "hyperoxaluria (lab test)", "High urine oxalate levels", "hyperoxaluria (diagnosis)", "Primary hyperoxaluria, NOS", "Primary hyperoxaluria (disorder)", "Primary hyperoxaluria (diagnosis)", "Increased level of oxalate in urine", "urine tests nonspecific abnormal findings hyperoxaluria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary hyperoxaluria", "shortest_name_length": 8}
{"curie": "MONDO:0019476", "names": ["primary cutaneous unspecified peripheral T-cell lymphoma", "primary cutaneous peripheral T-cell lymphoma not otherwise specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary cutaneous peripheral T-cell lymphoma not otherwise specified", "shortest_name_length": 56}
{"curie": "UMLS:C1711391", "names": ["Recurrent Hepatocellular Cancer", "Recurrent Adult Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Adult Hepatocellular Carcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C0346085", "names": ["Malignant Skin Hemangiopericytoma", "Malignant hemangiopericytoma of skin", "Malignant Hemangiopericytoma of Skin", "malignant hemangiopericytoma of skin", "Malignant haemangiopericytoma of skin", "Malignant Hemangiopericytoma of the Skin", "Malignant hemangiopericytoma of skin (disorder)", "malignant hemangiopericytoma of skin (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant hemangiopericytoma of skin", "shortest_name_length": 33}
{"curie": "MONDO:0031001", "names": ["VPED", "vitreoretinopathy with phalangeal epiphyseal dysplasia", "VITREORETINOPATHY WITH PHALANGEAL EPIPHYSEAL DYSPLASIA", "Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitreoretinopathy with phalangeal epiphyseal dysplasia", "shortest_name_length": 4}
{"curie": "MONDO:0014627", "names": ["DYT27", "dystonia 27", "DYSTONIA 27", "dystonia type 27", "COL6A3 dystonic disorder", "Primary dystonia type 27", "Primary dystonia DYT27 type", "Primary dystonia, DYT27 type", "primary dystonia, DYT27 type", "Primary dystonia type 27 (disorder)", "dystonic disorder caused by mutation in COL6A3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dystonia 27", "shortest_name_length": 5}
{"curie": "UMLS:C1698628", "names": ["Urostomy Site Bleeding", "Urostomy site bleeding", "Urostomy site bleeding (diagnosis)", "postprocedural complications urostomy site bleeding"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urostomy Site Bleeding", "shortest_name_length": 22}
{"curie": "UMLS:C1336147", "names": ["Stage IB Vulvar Cancer", "Stage IB Vulva Carcinoma AJCC v6", "Stage IB Vulvar Carcinoma AJCC v6", "Stage IB Carcinoma of Vulva AJCC v6", "Stage IB Carcinoma of the Vulva AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Vulvar Carcinoma AJCC v6", "shortest_name_length": 22}
{"curie": "UMLS:C4050504", "names": ["EMCMT", "Ectomesenchymal Chondromyxoid Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ectomesenchymal Chondromyxoid Tumor", "shortest_name_length": 5}
{"curie": "UMLS:C1261959", "names": ["respiratory tract infection bacterial", "bacterial respiratory tract infection", "Respiratory tract infection bacterial", "Bacterial infections of the respiratory tract", "bacterial respiratory tract infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Respiratory tract infection bacterial", "shortest_name_length": 37}
{"curie": "UMLS:C1167723", "names": ["Hepatic cancer stage III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatic cancer stage III", "shortest_name_length": 24}
{"curie": "MONDO:0021402", "names": ["External Ear Polyp", "external Ear polyp", "External Auditory Canal Polyp", "external auditory canal polyp", "external acoustic meatus polyp", "Polyp of external auditory canal", "polyp of external auditory canal", "Polyp of External Auditory Canal", "Polyp of external auditory meatus", "polyp of external auditory meatus", "Polyp of the External Auditory Canal", "polyp of the external auditory canal", "Aural polyp of external auditory canal", "Polyp of external auditory meatus (disorder)", "polyp of external auditory canal (diagnosis)", "polyp of external auditory meatus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyp of external auditory canal", "shortest_name_length": 18}
{"curie": "MONDO:0020324", "names": ["IVBCL", "IVLBCL", "Angiotropic lymphoma", "angiotropic lymphoma", "Angiotropic Lymphoma", "Angioendotheliomatosis", "angioendotheliomatosis", "Tappeiner-Pfleger disease", "Intravascular lymphomatosis", "intravascular lymphomatosis", "Intravascular B-cell lymphoma", "intravascular B-cell lymphoma", "Intravascular B-Cell Lymphoma", "Angiotropic large cell lymphoma", "Angiotropic Large Cell Lymphoma", "angiotropic large cell lymphoma", "malignant angioendotheliomatosis", "Malignant angioendotheliomatosis", "Malignant Angioendotheliomatosis", "Angioendotheliomatosis (diagnosis)", "intravascular large B-cell lymphoma", "Intravascular large B-cell lymphoma", "Intravascular Large B-Cell Lymphoma", "Intravascular large B-cell lymphoma (disorder)", "angioendotheliomatosis proliferans systemisata", "Angioendotheliomatosis proliferans systemisata", "Intravascular large B-cell lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intravascular large B-cell lymphoma", "shortest_name_length": 5}
{"curie": "MONDO:0008490", "names": ["WZS", "STL3", "OSMEDA", "AD OSMED", "STL3, FORMERLY", "heterozygous OSMED", "OSMED heterozygous", "Heterozygous Osmed", "OSMED, HETEROZYGOUS", "OSMED, heterozygous", "Piere-Robin syndrome", "type 3 Stickler syndrome", "Stickler syndrome type 3", "Pierre Robin malformation", "Pierre Robin Malformation", "COL11A2 Stickler syndrome", "Stickler syndrome, type 3", "STICKLER syndrome, type III", "Stickler Syndrome, Type III", "Stickler syndrome nonocular type", "Stickler Syndrome, Nonocular Type", "WEISSENBACHER-ZWEYMULLER SYNDROME", "Weissenbacher-Zweymüller syndrome", "Stickler syndrome non-ocular type", "Weissenbacher-Zweymuller syndrome", "Stickler syndrome, Nonocular type", "Weissenbacher-Zweymüller Syndrome", "Stickler syndrome, non-ocular type", "Weissenbacher- Zweymuller syndrome", "Stickler syndrome type 3 (disorder)", "type 3 Stickler syndrome (diagnosis)", "Stickler syndrome, type III, formerly", "STICKLER SYNDROME, TYPE III, FORMERLY", "Stickler syndrome caused by mutation in COL11A2", "heterozygous otospondylomegaepiphyseal dysplasia", "Heterozygous Otospondylomegaepiphyseal Dysplasia", "Pierre Robin syndrome with fetal chondrodysplasia", "Pierre Robin sequence-fetal chondrodysplasia syndrome", "Pierre Robin syndrome-fetal chondrodysplasia syndrome", "Autosomal dominant otospondylomegaepiphyseal dysplasia", "OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT", "otospondylomegaepiphyseal dysplasia, autosomal dominant", "AD OSMED - autosomal dominant otospondylomegaepiphyseal dysplasia", "Pierre Robin syndrome with fetal chondrodysplasia Stickler syndrome, Nonocular type", "PIERRE ROBIN SYNDROME WITH FETAL CHONDRODYSPLASIA STICKLER SYNDROME, NONOCULAR TYPE, FORMERLY", "Pierre Robin syndrome with fetal chondrodysplasia Stickler syndrome, Nonocular type, formerly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "otospondylomegaepiphyseal dysplasia, autosomal dominant", "shortest_name_length": 3}
{"curie": "MONDO:0001829", "names": ["lumbosacral plexus lesion", "Lumbosacral plexus lesion", "lumbosacral plexus lesions", "Lumbosacral plexus lesions", "lesion; lumbosacral plexus", "lumbosacral plexus; lesion", "lesion; lumbosacral, plexus", "plexus lumbosacralis; lesion", "Lumbosacral plexus lesion, NOS", "Lumbosacral plexus lesion (disorder)", "lumbosacral plexus lesion (diagnosis)", "lumbosacral nerve plexus nerve plexus disease", "nerve plexus disease of lumbosacral nerve plexus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lumbosacral plexus lesion", "shortest_name_length": 25}
{"curie": "MONDO:0015457", "names": ["Ben Ari-Shuper-Mimouni syndrome", "Ben Ari Shuper Mimouni syndrome", "corpus callosum agenesis double urinary collecting", "corpus callosum agenesis - double urinary collecting system", "corpus callosum agenesis-double urinary collecting system syndrome", "agenesis of corpus callosum with double urinary collecting system, trigonocephaly and minor anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corpus callosum agenesis-double urinary collecting system syndrome", "shortest_name_length": 31}
{"curie": "UMLS:C1332199", "names": ["Desmoplastic Small Round Cell Tumor", "adult desmoplastic small round cell tumor", "Adult Desmoplastic Small Round Cell Tumor", "tumor, desmoplastic small round cell, adult", "small round cell tumor, desmoplastic, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Desmoplastic Small Round Cell Tumor", "shortest_name_length": 35}
{"curie": "UMLS:C0478077", "names": ["Other osteochondrodysplasia with defects of growth of tubular bones and spine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Other osteochondrodysplasia with defects of growth of tubular bones and spine", "shortest_name_length": 77}
{"curie": "MONDO:0004903", "names": ["deep keratitis", "Deep keratitis", "deep; keratitis", "keratitis; deep", "deep keratitis (diagnosis)", "Interstitial and deep keratitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deep keratitis", "shortest_name_length": 14}
{"curie": "UMLS:C5235846", "names": ["Locally Advanced PitNET", "Locally Advanced Pituitary Gland Carcinoma", "Locally Advanced Pituitary Neuroendocrine Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Pituitary Neuroendocrine Tumor", "shortest_name_length": 23}
{"curie": "MONDO:0002350", "names": ["Congenital nephrosis", "Nephrosis, congenital", "Familial nephrotic syndrome", "familial nephrotic syndrome", "congenital nephrotic syndrome", "Congenital nephrotic syndrome", "hereditary nephrotic syndrome", "Congenital Nephrotic Syndrome", "Nephrotic syndrome, congenital", "Congenital nephrotic syndrome (disorder)", "congenital nephrotic syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial nephrotic syndrome", "shortest_name_length": 20}
{"curie": "MONDO:0005571", "names": ["Polycythemia", "polycythemia", "POLYCYTHEMIA", "Polyglobulia", "polycythaemia", "Polycythaemia", "POLYCYTHAEMIA", "Polycythemias", "Erythrocytosis", "erythrocytosis", "Erythrocytoses", "ERYTHROCYTOSIS", "erythrocythemia", "Erythrocythemia", "Polycythemia NOS", "Erythrocythaemia", "Polycythemia, NOS", "Polycythaemia NOS", "Erythrocytosis NOS", "Polycythaemia, NOS", "polycythemia (disease)", "polycythemia (diagnosis)", "Increased red blood cells", "Erythrocytosis (disorder)", "Abnormally shaped erythrocytes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polycythemia", "shortest_name_length": 12}
{"curie": "MONDO:0015805", "names": ["Intestinal botulism", "intestinal botulism", "Intestinal toxemia botulism", "intestinal toxemia botulism", "Intestinal botulism (disorder)", "intestinal colonization botulism", "Intestinal colonization botulism", "Intestinal toxin-mediated botulism", "intestinal toxin-mediated botulism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intestinal botulism", "shortest_name_length": 19}
{"curie": "MESH:D003921", "names": ["Diabetes Mellitus, Experimental"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diabetes Mellitus, Experimental", "shortest_name_length": 31}
{"curie": "MONDO:0030030", "names": ["NIZIDS", "nizon-isidor syndrome", "Nizon-Isidor syndrome", "NIZON-ISIDOR SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nizon-Isidor syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0015195", "names": ["atresia; urethra", "urethra; atresia", "Urethral atresia", "urethral atresia", "Atresia of urethra", "atresia of urethra", "urethra; imperforate", "imperforate; urethra", "Absent urethral opening", "Urethral opening absent", "atresia of urethra (disease)", "Atresia of urethra (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atresia of urethra", "shortest_name_length": 16}
{"curie": "MONDO:0005988", "names": ["Toxocarosis", "toxocarosis", "toxocariasis", "Toxocariasis", "TOXOCARIASIS", "Toxocariases", "Toxocara infection", "Visceral Larva Migrans", "visceral larva migrans", "infection by Toxascaris", "Infection by Toxascaris", "toxocariasis (diagnosis)", "Infection due to Toxocara", "Toxocara infectious disease", "Toxocara disease or disorder", "Infection caused by Toxocara", "Toxocara caused disease or disorder", "Infection caused by Toxocara (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "toxocariasis", "shortest_name_length": 11}
{"curie": "MONDO:0014731", "names": ["SSMS", "SSM syndrome", "seizures-scoliosis-macrocephaly syndrome", "Seizures-scoliosis-macrocephaly syndrome", "Seizures, scoliosis, macrocephaly syndrome", "SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME", "seizures, scoliosis, and macrocephaly syndrome", "SSM (seizures, scoliosis, macrocephaly) syndrome", "Seizures, scoliosis, macrocephaly syndrome (disorder)", "SEIZURES, SCOLIOSIS, AND MACROCEPHALY/MICROCEPHALY SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "seizures-scoliosis-macrocephaly syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0018031", "names": ["Granulomatous slack skin", "Granulomatous Slack Skin", "granulomatous slack skin", "Slack Skin, Granulomatous", "Granulomatous slack skin disease", "Granulomatous Slack Skin Disease", "granulomatous slack skin disease", "Granulomatous slack skin disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "granulomatous slack skin disease", "shortest_name_length": 24}
{"curie": "UMLS:C4521865", "names": ["Stage IB Ampulla of Vater Cancer", "Stage IB Ampulla of Vater Cancer AJCC v8", "Stage IB Ampulla of Vater Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Ampulla of Vater Cancer AJCC v8", "shortest_name_length": 32}
{"curie": "MONDO:0013234", "names": ["HOKPP2", "hypokalemic periodic paralysis type 2", "hypokalemic periodic paralysis, type 2", "Hypokalemic Periodic Paralysis, Type 2", "HYPOKALEMIC PERIODIC PARALYSIS, TYPE 2", "hypokalemic periodic paralysis type 2 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypokalemic periodic paralysis, type 2", "shortest_name_length": 6}
{"curie": "UMLS:C0338810", "names": ["Subchronic latent schizophrenia", "latent subchronic schizophrenia", "Latent Subchronic Schizophrenia", "Latent schizophrenia, subchronic", "Latent schizophrenia, subchronic state", "Subchronic latent schizophrenia (disorder)", "latent subchronic schizophrenia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subchronic latent schizophrenia", "shortest_name_length": 31}
{"curie": "MONDO:0008523", "names": ["EOS", "ACUG", "BLAUS", "BLAU SYNDROME", "JABS SYNDROME", "Jabs syndrome", "Blau syndrome", "Blau Syndrome", "blau syndrome sporadic", "Sporadic Blau syndrome", "Early onset sarcoidosis", "Early-Onset Sarcoidosis", "early-onset sarcoidosis", "sarcoidosis, early-onset", "SARCOIDOSIS, EARLY-ONSET", "Blau syndrome (disorder)", "Sarcoidosis, Early-Onset", "Blau syndrome (diagnosis)", "Arthrocutaneouveal granulamotosis", "arthrocutaneouveal granulomatosis", "Arthrocutaneouveal granulomatosis", "Sporadic Blau syndrome (disorder)", "ARTHROCUTANEOUVEAL GRANULOMATOSIS", "pediatric granulomatous arthritis", "Pediatric Granulomatous Arthritis", "Pediatric granulomatous arthritis", "Familial granulomatosis, Blau type", "Familial Granulomatosis, Blau Type", "Paediatric granulomatous arthritis", "Sporadic Blau syndrome (diagnosis)", "Granulomatosis, familial, Blau type", "granulomatosis, familial, Blau type", "GRANULOMATOSIS, FAMILIAL, BLAU TYPE", "Familial juvenile systemic granulomatosis", "Familial Juvenile Systemic Granulomatosis", "GRANULOMATOSIS, FAMILIAL JUVENILE SYSTEMIC", "Granulomatosis, familial juvenile systemic", "granulomatosis, familial juvenile systemic", "Synovitis granulomatous with uveitis and cranial neuropathies", "synovitis granulomatous with uveitis and cranial neuropathies", "synovitis, granulomatous, with uveitis and cranial neuropathies", "Synovitis, Granulomatous, With Uveitis And Cranial Neuropathies", "familial granulomatous inflammatory arthritis, dermatitis and uveitis", "Familial granulomatous inflammatory arthritis, dermatitis and uveitis", "Granulomatous inflammatory arthritis, dermatitis and uveitis, familial", "granulomatous inflammatory arthritis, dermatitis, and uveitis, familial", "Granulomatous inflammatory arthritis, dermatitis, and uveitis, familial", "GRANULOMATOUS INFLAMMATORY ARTHRITIS, DERMATITIS, AND UVEITIS, FAMILIAL", "SYNOVITIS, GRANULOMATOUS, WITH UVEITIS AND CRANIAL NEUROPATHIES (disorder)", "Familial granulomatous inflammatory arthritis, dermatitis and uveitis (disorder)", "familial granulomatous inflammatory arthritis, dermatitis and uveitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Blau syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0012361", "names": ["SLEB5", "SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 5", "systemic lupus erythematosus, susceptibility to, 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "systemic lupus erythematosus, susceptibility to, 5", "shortest_name_length": 5}
{"curie": "MONDO:0007043", "names": ["ACS5", "ACS 5", "ACS V", "NOACK SYNDROME", "Noack syndrome", "Noack Syndrome", "Syndrome, Noack", "Noack Syndromes", "Syndromes, Noack", "pfeiffer syndrome", "Pfeiffer syndrome", "Pfeiffer Syndrome", "PFEIFFER SYNDROME", "pfeiffers syndrome", "Syndrome, Pfeiffer", "Pfeiffer's syndrome", "pfeiffer's syndrome", "Oto-onychoperoneal syndrome", "Type V Acrocephalosyndactyly", "Acrocephalosyndactyly type V", "acrocephalosyndactyly type 5", "acrocephalosyndactyly type V", "type V Acrocephalosyndactyly", "Acrocephalosyndactyly type 5", "Acrocephalosyndactyly Type V", "acrocephalosyndactyly, type 5", "Acrocephalosyndactyly, Type V", "acrocephalosyndactylia type V", "ACROCEPHALOSYNDACTYLY, TYPE V", "Type V Acrocephalosyndactylies", "Acrocephalosyndactylies, Type V", "Pfeiffer-type acrocephalosyndactyly", "Pfeiffer type acrocephalosyndactyly", "Pfeiffer syndrome - oto-onychoperoneal", "Acrocephalosyndactyly type V (disorder)", "CRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA", "Pfeiffer type acrocephalosyndactyly, type II", "craniofacial-skeletal-Dermatologic dysplasia", "Craniofacial-Skeletal-Dermatologic Dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pfeiffer syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0015371", "names": ["Linear atrophoderma of Moulin", "linear atrophoderma of Moulin", "Linear atrophoderma of Moulin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "linear atrophoderma of Moulin", "shortest_name_length": 29}
{"curie": "MONDO:0034021", "names": ["spondylodysplastic EDS", "spondylodysplastic Ehlers-Danlos syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondylodysplastic Ehlers-Danlos syndrome", "shortest_name_length": 22}
{"curie": "UMLS:C4722419", "names": ["ESCC", "Extrapulmonary SCC", "Small cell car. (extrapulmonary)", "Extrapulmonary Small Cell Carcinoma", "Small cell carcinoma (extrapulmonary)", "Extrapulmonary Small Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extrapulmonary Small Cell Carcinoma", "shortest_name_length": 4}
{"curie": "UMLS:C0948777", "names": ["Necrotizing esophagitis", "Necrotising oesophagitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Necrotizing esophagitis", "shortest_name_length": 23}
{"curie": "UMLS:C0598589", "names": ["Inherited Neuropathy", "inherited neuropathy", "neuropathy hereditary", "hereditary neuropathy", "neuropathy; hereditary", "Inherited neuropathies", "inherited neuropathies", "hereditary neuropathies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Inherited neuropathies", "shortest_name_length": 20}
{"curie": "MONDO:0003001", "names": ["seminoma", "Seminoma", "seminoma, pure", "Seminoma, Pure", "seminoma, malignant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "seminoma", "shortest_name_length": 8}
{"curie": "MONDO:0014261", "names": ["COXPD18", "combined oxidative phosphorylation deficiency 18", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 18", "SFXN4 combined oxidative phosphorylation deficiency", "combined oxidative phosphorylation deficiency type 18", "combined oxidative phosphorylation deficiency caused by mutation in SFXN4", "growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome", "shortest_name_length": 7}
{"curie": "UMLS:C0393750", "names": ["External Compression Headache", "External compression headache", "Headache due to external compression of head", "Headache due to external compression of head (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Headache due to external compression of head", "shortest_name_length": 29}
{"curie": "MONDO:0023551", "names": ["C1q nephropathy", "C1q nephropathy (disorder)", "C1q nephropathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "C1q nephropathy", "shortest_name_length": 15}
{"curie": "MONDO:0018016", "names": ["classic appendix neuroendocrine tumor", "classic appendiceal neuroendocrine tumor", "classic neuroendocrine tumor of appendix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "classic neuroendocrine tumor of appendix", "shortest_name_length": 37}
{"curie": "UMLS:C0334376", "names": ["Intracystic carcinoma", "Intracystic carcinoma NOS", "Intracystic carcinoma, NOS", "Intracystic Breast Carcinoma", "intracystic carcinoma of breast", "Intracystic Papillary Adenocarcinoma", "Intracystic papillary adenocarcinoma", "Breast Intracystic Papillary Carcinoma", "Intracystic Papillary Breast Carcinoma", "intracystic carcinoma of breast (diagnosis)", "Noninfiltrating Intracystic Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intracystic Papillary Breast Carcinoma", "shortest_name_length": 21}
{"curie": "MONDO:0016058", "names": ["Episodic dystonia", "Dystonia, episodic", "Paroxysmal dystonia", "Paroxysmal Dystonia", "paroxysmal dystonia", "dystonias paroxysmal", "Dystonia, paroxysmal", "Dystonia, Paroxysmal", "Paroxysmal dystonia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paroxysmal dystonia", "shortest_name_length": 17}
{"curie": "UMLS:C2217038", "names": ["Stage IIIB Colon Cancer", "Stage IIIB Colon Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Colon Cancer AJCC v7", "shortest_name_length": 23}
{"curie": "MONDO:0100101", "names": ["FADS1", "Pena-Shokeir syndrome type 1", "Pena-Shokeir syndrome, type 1", "fetal akinesia deformation sequence 1", "fetal akinesia deformation sequence syndrome 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fetal akinesia deformation sequence 1", "shortest_name_length": 5}
{"curie": "MONDO:0006420", "names": ["small bowel MALToma", "Small Bowel MALToma", "MALToma of Small Bowel", "MALToma of small bowel", "small intestine MALToma", "Small Intestine MALToma", "Small Bowel MALT Lymphoma", "small bowel MALT lymphoma", "MALToma of Small Intestine", "MALToma of small intestine", "MALToma of the Small Bowel", "MALToma of the small bowel", "MALT lymphoma of small bowel", "MALT Lymphoma of Small Bowel", "small intestine MALT lymphoma", "Small Intestine MALT Lymphoma", "MALToma of the small intestine", "MALToma of the Small Intestine", "MALT lymphoma of small intestine", "MALT lymphoma of the small bowel", "MALT Lymphoma of the Small Bowel", "MALT Lymphoma of Small Intestine", "MALT Lymphoma of the Small Intestine", "MALT lymphoma of the small intestine", "small bowel mucosa-associated lymphoid tissue lymphoma", "Small Bowel Mucosa-Associated Lymphoid Tissue Lymphoma", "mucosa-associated lymphoid tissue lymphoma of small bowel", "Mucosa-Associated Lymphoid Tissue Lymphoma of Small Bowel", "small intestine mucosa-associated lymphoid tissue lymphoma", "Small Intestine Mucosa-Associated Lymphoid Tissue Lymphoma", "Small Intestinal Mucosa-Associated Lymphoid Tissue Lymphoma", "small intestinal mucosa-associated lymphoid tissue lymphoma", "mucosa-associated lymphoid tissue lymphoma of small intestine", "Mucosa-Associated Lymphoid Tissue Lymphoma of the Small Bowel", "Mucosa-Associated Lymphoid Tissue Lymphoma of Small Intestine", "mucosa-associated lymphoid tissue lymphoma of the small bowel", "mucosa-associated lymphoid tissue lymphoma of the small intestine", "Mucosa-Associated Lymphoid Tissue Lymphoma of the Small Intestine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small intestinal mucosa-associated lymphoid tissue lymphoma", "shortest_name_length": 19}
{"curie": "MONDO:0013682", "names": ["VUR4", "VESICOURETERAL REFLUX 4", "vesicoureteral reflux 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vesicoureteral reflux 4", "shortest_name_length": 4}
{"curie": "MONDO:0010140", "names": ["TRH DEFICIENCY", "TRH deficiency", "Isolated TRF deficiency", "Isolated TRH deficiency", "tertiary hypothyroidism", "isolated TRH deficiency", "isolated TRF deficiency", "Tertiary Hypothyroidism", "Tertiary hypothyroidism", "hypothalamic hypothyroidism", "HYPOTHALAMIC HYPOTHYROIDISM", "Hypothalamic Hypothyroidism", "Hypothalamic hypothyroidism", "HYPOTHYROIDISM, HYPOTHALAMIC", "isolated protirelin deficiency", "Isolated protirelin deficiency", "Isolated thyroliberin deficiency", "isolated thyroliberin deficiency", "isolated prothyroliberin deficiency", "Isolated prothyroliberin deficiency", "Hypothyroidism due to TRH deficiency", "Hypothalamic hypothyroidism (disorder)", "THYROTROPIN-RELEASING HORMONE DEFICIENCY", "Isolated TSH-releasing factor deficiency", "thyrotropin-releasing hormone deficiency", "isolated TSH-releasing factor deficiency", "Isolated thyroliberin deficiency (disorder)", "Isolated thyrotropin-releasing factor deficiency", "isolated thyrotropin-releasing factor deficiency", "isolated thyrotropin-releasing hormone deficiency", "Isolated thyrotropin-releasing hormone deficiency", "Isolated thyroid hormone releasing hormone deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated thyrotropin-releasing hormone deficiency", "shortest_name_length": 14}
{"curie": "MONDO:0003168", "names": ["cerebellum pilocytic astrocytoma", "Cerebellar Pilocytic Astrocytoma", "Cerebellar Pilocytic astrocytoma", "cerebellar pilocytic astrocytoma", "Pilocytic astrocytoma of cerebellum", "Pilocytic Astrocytoma of Cerebellum", "pilocytic astrocytoma of cerebellum", "Pilocytic Astrocytoma of the Cerebellum", "pilocytic astrocytoma of the cerebellum", "Pilocytic astrocytoma of cerebellum (disorder)", "pilocytic astrocytoma of cerebellum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellar pilocytic astrocytoma", "shortest_name_length": 32}
{"curie": "UMLS:C0236065", "names": ["Mouth edema", "mouth edema", "edema mouth", "EDEMA MOUTH", "Edema mouth", "Mouth oedema", "Oedema mouth", "OEDEMA MOUTH", "Edema of mouth", "Oedema of mouth", "Edema of oral soft tissues", "Oedema of oral soft tissues", "Edema of oral soft tissues (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Edema of mouth", "shortest_name_length": 11}
{"curie": "MONDO:0003234", "names": ["optic tract astrocytoma", "optic nerve astrocytoma", "Optic Nerve Astrocytoma", "Astrocytoma of Optic Nerve", "astrocytoma of optic nerve", "Astrocytoma of the Optic Nerve", "astrocytoma of the optic nerve", "Astrocytic tumor of optic nerve", "astrocytic tumor of optic nerve", "optic tract astrocytoma (excluding glioblastoma)", "cranial nerve II astrocytoma (excluding glioblastoma)", "astrocytoma (excluding glioblastoma) of cranial nerve II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "optic nerve astrocytoma", "shortest_name_length": 23}
{"curie": "UMLS:C1318512", "names": ["esophagus injury", "injury of esophagus without open wound into thoracic cavity", "Injury of esophagus without open wound into thoracic cavity", "Injury to esophagus without mention of open wound into cavity", "Injury to Esophagus without mention of Open Wound into Cavity", "Injury to oesophagus without mention of open wound into cavity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of esophagus without open wound into thoracic cavity", "shortest_name_length": 16}
{"curie": "UMLS:C0392164", "names": ["Cystic fibrosis lung", "cystic fibrosis lung", "CYSTIC FIBROSIS LUNG", "cystic fibrosis lungs", "cystic fibrosis of lung", "Pulmonary cystic fibrosis", "pulmonary cystic fibrosis", "Pulmonary Cystic Fibrosis", "Cystic Fibrosis, Pulmonary", "Cystic fibrosis of the lung", "Mucoviscidosis involving the lung", "cystic fibrosis of lung (diagnosis)", "Cystic fibrosis of the lung (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pulmonary Cystic Fibrosis", "shortest_name_length": 20}
{"curie": "UMLS:C1096083", "names": ["Extraocular muscle disorder", "Disorder of extraocular muscle", "Disorder of extraocular muscle (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disorder of extraocular muscle", "shortest_name_length": 27}
{"curie": "MONDO:0012948", "names": ["monosomy 6p25", "Monosomy 6p25", "distal deletion 6p", "Distal deletion 6p", "distal monosomy 6p", "Distal monosomy 6p", "distal monosomy type 6p", "6p25 microdeletion syndrome", "Distal monosomy 6p (disorder)", "Distal monosomy 6p (diagnosis)", "6p subtelomeric deletion syndrome", "CHROMOSOME 6pter-p24 DELETION SYNDROME", "chromosome 6pter-p24 deletion syndrome", "Chromosome 6pter-P24 Deletion Syndrome", "deletion of part of chromosome distal monosomy 6p", "chromosome 6pter-p24 deletion syndrome, isolated cases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 6pter-p24 deletion syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0007686", "names": ["GPS", "BDPLT4", "Grey Platelet Syndrome", "Grey platelet syndrome", "GRAY PLATELET SYNDROME", "Gray platelet syndrome", "gray platelet syndrome", "grey platelet syndrome", "Gray Platelet Syndrome", "Syndrome, Grey Platelet", "Grey Platelet Syndromes", "Platelet granule defect", "Gray Platelet Syndromes", "Syndrome, Gray Platelet", "Platelet Syndromes, Grey", "Syndromes, Gray Platelet", "gray; syndrome, platelets", "syndrome; gray, platelets", "Alpha storage pool deficiency", "Deficient alpha granule syndrome", "platelet-type bleeding disorder 4", "platelet alpha-granule deficiency", "Platelet alpha granule deficiency", "Platelet alpha Granule Deficiency", "PLATELET ALPHA-GRANULE DEFICIENCY", "Platelet alpha-Granule Deficiency", "Gray platelet syndrome (disorder)", "Platelet alpha-granule deficiency", "alpha-Granule Deficiency, Platelet", "Platelet alpha-Granule Deficiencies", "BLEEDING DISORDER, PLATELET-TYPE, 4", "bleeding disorder, Platelet-type, 4", "alpha-Granule Deficiencies, Platelet", "marked decrease or absence of alpha-granules and of platelet-specific alpha-granule proteins"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gray platelet syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0100266", "names": ["PEX12 related Zellweger spectrum disorder", "peroxisome biogenesis disorder due to PEX12 defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder due to PEX12 defect", "shortest_name_length": 41}
{"curie": "MONDO:0003830", "names": ["type 1 renal papillary adenoma", "Type 1 Renal Papillary Adenoma", "type 1 papillary adenoma of the kidney", "Type 1 Papillary Adenoma of the Kidney"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type 1 papillary adenoma of the kidney", "shortest_name_length": 30}
{"curie": "MONDO:0011766", "names": ["GDMN", "46XY gonadal dysgenesis with minifascicular neuropathy", "46,XY GONADAL DYSGENESIS WITH MINIFASCICULAR NEUROPATHY", "46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome", "46,XY gonadal dysgenesis, partial, with MINIFASCICULAR neuropathy", "46,Xy Gonadal Dysgenesis, Partial, With Minifascicular Neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C2064241", "names": ["Anal Small Cell NEC", "Anal Canal Small Cell NEC", "Anal Canal Small Cell Carcinoma", "small cell carcinoma of anal canal", "Anal Small Cell Neuroendocrine Carcinoma", "small cell carcinoma of anal canal (diagnosis)", "Anal Canal Small Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small cell carcinoma of anal canal", "shortest_name_length": 19}
{"curie": "UMLS:C5447369", "names": ["Recurrent Breast Implant-Associated Anaplastic Large Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Breast Implant-Associated Anaplastic Large Cell Lymphoma", "shortest_name_length": 66}
{"curie": "UMLS:C3146247", "names": ["Stage II Renal Cell Cancer", "Stage II Renal Cell Carcinoma", "Stage II Renal Cell Cancer AJCC v7", "Stage II Renal Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Renal Cell Cancer AJCC v7", "shortest_name_length": 26}
{"curie": "UMLS:C0280733", "names": ["recurrent CUP", "CUP, recurrent", "Recurrent Carcinoma of Unknown Primary", "recurrent carcinoma of unknown primary", "carcinoma of unknown primary, recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Carcinoma of Unknown Primary", "shortest_name_length": 13}
{"curie": "UMLS:C1167721", "names": ["stage II pancreas cancer", "pancreas cancer, stage II", "stage II pancreatic cancer", "pancreatic cancer, stage II", "Pancreatic carcinoma stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic carcinoma stage II", "shortest_name_length": 24}
{"curie": "UMLS:C0269252", "names": ["Apocrine metaplasia of breast", "Apocrine Metaplasia of Breast", "Apocrine metaplasia of breast (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Apocrine metaplasia of breast", "shortest_name_length": 29}
{"curie": "MONDO:0005699", "names": ["lumpy jaw", "Lumpy jaw", "jaw lumpy", "cervicofacial actinomycosis", "Cervicofacial actinomycosis", "CERVICOFACIAL ACTINOMYCOSIS", "Actinomycosis, cervicofacial", "cervicofacial; actinomycosis", "actinomycosis; cervicofacial", "Actinomycosis, Cervicofacial", "Cervicofacial Actinomycotic Infection", "Cervicofacial actinomycotic infection", "cervicofacial actinomycotic infection", "Cervicofacial actinomycosis (disorder)", "cervicofacial actinomycosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervicofacial actinomycosis", "shortest_name_length": 9}
{"curie": "MONDO:0017585", "names": ["painful orbital and systemic neurofibromas-marfanoid habitus syndrome", "multiple orbital neurofibromas, painful peripheral nerve tumors, distinctive face and marfanoid habitus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "painful orbital and systemic neurofibromas-marfanoid habitus syndrome", "shortest_name_length": 69}
{"curie": "UMLS:C0863087", "names": ["Decreased immune responsiveness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Decreased immune responsiveness", "shortest_name_length": 31}
{"curie": "UMLS:C1336922", "names": ["AIDS-Related Burkitt Lymphoma with Plasmacytoid Differentiation", "AIDS-Related Burkitt's Lymphoma with Plasmacytoid Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Burkitt Lymphoma with Plasmacytoid Differentiation", "shortest_name_length": 63}
{"curie": "MONDO:0014417", "names": ["SCA38", "SPINOCEREBELLAR ATAXIA 38", "spinocerebellar ataxia 38", "spinocerebellar ataxia type 38", "Spinocerebellar ataxia type 38", "Spinocerebellar ataxia type 38 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia type 38", "shortest_name_length": 5}
{"curie": "UMLS:C4054083", "names": ["Refractory Malignant Germ Cell Tumor", "Refractory Malignant Germ Cell Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Malignant Germ Cell Tumor", "shortest_name_length": 36}
{"curie": "UMLS:C1332593", "names": ["Borderline Exocrine Pancreatic Tumor", "Borderline Tumor of Exocrine Pancreas", "Borderline Exocrine Pancreatic Neoplasm", "Borderline Neoplasm of Exocrine Pancreas", "Borderline Tumor of the Exocrine Pancreas", "Borderline Neoplasm of the Exocrine Pancreas", "Exocrine Pancreatic Tumor of Uncertain Malignant Potential", "Tumor of Uncertain Malignant Potential of Exocrine Pancreas", "Exocrine Pancreatic Neoplasm of Uncertain Malignant Potential", "Neoplasm of Uncertain Malignant Potential of Exocrine Pancreas", "Tumor of Uncertain Malignant Potential of the Exocrine Pancreas", "Neoplasm of Uncertain Malignant Potential of the Exocrine Pancreas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Exocrine Pancreatic Neoplasm", "shortest_name_length": 36}
{"curie": "MONDO:0005834", "names": ["LGV", "lgv", "Frei", "FREI DISEASE", "Strumous bubo", "strumous bubo", "Favre-Nicolas", "climatic; bubo", "tropical; bubo", "BUBO, CLIMATIC", "bubo; tropical", "bubo; climactic", "PORADENITIS NOSTRAS", "poradenitis; nostras", "Durand-Nicolas-Favre", "FAVRE-DURAND DISEASE", "lymphopathia venereum", "Lymphopathia venereum", "Nicolas-Favre disease", "Poradenitis inguinale", "LYMPHOPATHIA VENEREUM", "Nicholas Favre disease", "Chlamydia; lymphadenitis", "Lymphogranuloma Venereum", "Lymphogranuloma venereum", "LYMPHOGRANULOMA VENEREUM", "lymphogranuloma venereum", "Lymphogranuloma inguinale", "lymphogranuloma inguinale", "Lymphogranuloma Inguinale", "climatic or tropical bubo", "lymphogranuloma; venereum", "venereum; lymphogranuloma", "lymph granuloma inguinale", "LYMPHOGRANULOMA INGUINALE", "Climatic or tropical bubo", "inguinal; lymphogranuloma", "lymphogranuloma; inguinale", "Chlamydia; lymphogranuloma", "lymphogranuloma; chlamydial", "DURAND-NICOLAS-FAVRE DISEASE", "Durand-Nicolas-Favre disease", "LGV - Lymphogranuloma venereum", "nicolas(-Durand)-Favre disease", "chlamydial lymphogranuloma venereum", "Lymphogranuloma venereum (disorder)", "Chlamydia trachomatis lymphadenitis", "Chlamydial lymphogranuloma (venereum)", "chlamydial infections lymphogranuloma venereum", "chlamydial lymphogranuloma venereum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphogranuloma venereum", "shortest_name_length": 3}
{"curie": "MONDO:0022999", "names": ["distichiasis heart congenital anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distichiasis heart congenital anomalies", "shortest_name_length": 39}
{"curie": "MONDO:0002229", "names": ["OVT", "ovary epithelial cancer", "Ovarian Epithelial Tumor", "ovarian epithelial tumor", "Epithelial tumor of ovary", "epithelial tumor of ovary", "ovary epithelial neoplasm", "Epithelial Tumor of Ovary", "Epithelial tumour of ovary", "ovarian neoplasm epithelial", "Epithelial Neoplasm of Ovary", "epithelial neoplasm of ovary", "epithelial tumor of the ovary", "Epithelial Tumor of the Ovary", "epithelial neoplasm of the ovary", "Epithelial Neoplasm of the Ovary", "Epithelial tumor of ovary (disorder)", "epithelial neoplasm of ovary (diagnosis)", "Ovarian Surface Epithelial-Stromal Tumor", "Ovarian Surface epithelial-Stromal tumor", "ovarian surface epithelial-stromal tumor", "ovarian surface-epithelial stromal neoplasm", "Ovarian Surface-Epithelial Stromal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian epithelial tumor", "shortest_name_length": 3}
{"curie": "UMLS:C0279598", "names": ["TdT positive adult ALL", "adult ALL, TdT positive", "TdT positive ALL, adult", "ALL, adult TdT positive", "ALL, TdT positive, adult", "TdT Positive Acute Lymphoblastic Leukemia", "TdT positive adult acute lymphocytic leukemia", "TdT positive acute lymphocytic leukemia, adult", "leukemia, adult acute lymphocytic TdT positive", "acute lymphocytic leukemia, adult TdT positive", "TdT positive lymphocytic leukemia, acute adult", "TdT positive adult acute lymphoblastic leukemia", "Adult TdT Positive Acute Lymphoblastic Leukemia", "acute lymphoblastic leukemia, adult TdT positive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult TdT Positive Acute Lymphoblastic Leukemia", "shortest_name_length": 22}
{"curie": "UMLS:C0334087", "names": ["Cartilaginous hamartoma", "Cartilaginous Hamartoma", "Hamartoma, cartilaginous", "Cartilaginous hamartoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cartilaginous hamartoma", "shortest_name_length": 23}
{"curie": "MONDO:0014779", "names": ["WT6", "WILMS TUMOR 6", "Wilms tumor 6", "Wilms tumor type 6", "Wilms tumor 6; WT6", "Wilms tumor 6, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wilms tumor 6", "shortest_name_length": 3}
{"curie": "MONDO:0018243", "names": ["intellectual disability-hyperkinetic movement-truncal ataxia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability-hyperkinetic movement-truncal ataxia syndrome", "shortest_name_length": 69}
{"curie": "MONDO:0009974", "names": ["FEL", "FHL", "HLH1", "Hlh1", "FHL1", "HPLH", "FHLH", "HPLH1", "Hplh1", "Familial HLH", "familial HLH", "Familial Histiocytic Reticulosis", "Familial Histiocytic Reticuloses", "Familial histiocytic reticulosis", "RETICULOSIS, FAMILIAL HISTIOCYTIC", "Histiocytic Reticulosis, Familial", "Histiocytic Reticuloses, Familial", "Reticuloses, Familial Histiocytic", "reticulosis, familial histiocytic", "Reticulosis, Familial Histiocytic", "Familial Hemophagocytic Reticuloses", "Familial hemophagocytic reticulosis", "Familial Hemophagocytic Reticulosis", "familial hemophagocytic reticulosis", "HEMOPHAGOCYTIC RETICULOSIS, FAMILIAL", "hemophagocytic reticulosis, familial", "Reticuloses, Familial Hemophagocytic", "Hemophagocytic Reticuloses, Familial", "Hemophagocytic Reticulosis, Familial", "Reticulosis, Familial Hemophagocytic", "Familial haemophagocytic reticulosis", "Familial Hemophagocytic Lymphocytoses", "Familial hemophagocytic histiocytosis", "Familial Hemophagocytic Histiocytosis", "Familial Hemophagocytic Lymphocytosis", "Familial Hemophagocytic Histiocytoses", "Hemophagocytic Lymphocytosis, Familial", "Familial haemophagocytic histiocytosis", "Hemophagocytic Lymphocytoses, Familial", "Hemophagocytic Histiocytosis, Familial", "Hemophagocytic Histiocytoses, Familial", "Lymphocytosis, Familial Hemophagocytic", "Lymphocytoses, Familial Hemophagocytic", "Histiocytoses, Familial Hemophagocytic", "Histiocytosis, Familial Hemophagocytic", "Primary Hemophagocytic Hymphohistiocytoses", "Primary Hemophagocytic Lymphohistiocytoses", "Primary Hemophagocytic Hymphohistiocytosis", "Primary hemophagocytic lymphohistiocytosis", "Primary Hemophagocytic Lymphohistiocytosis", "Genetic hemophagocytic lymphohistiocytosis", "Lymphohistiocytosis, Primary Hemophagocytic", "familial hemophagocytic lymphohistiocytosis", "Primary haemophagocytic lymphohistiocytosis", "Lymphohistiocytoses, Primary Hemophagocytic", "Hemophagocytic Lymphohistiocytosis, Primary", "Hemophagocytic Hymphohistiocytoses, Primary", "Familial hemophagocytic lymphohistiocytosis", "Familial Hemophagocytic Lymphohistiocytoses", "Familial Hemophagocytic Lymphohistiocytosis", "Hemophagocytic Lymphohistiocytoses, Primary", "Hymphohistiocytoses, Primary Hemophagocytic", "Hemophagocytic Hymphohistiocytosis, Primary", "Genetic haemophagocytic lymphohistiocytosis", "Hymphohistiocytosis, Primary Hemophagocytic", "Hemophagocytic Lymphohistiocytoses, Familial", "Hemophagocytic Lymphohistiocytosis, Familial", "Lymphohistiocytoses, Familial Hemophagocytic", "HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL", "hemophagocytic lymphohistiocytosis, familial", "Familial haemophagocytic lymphohistiocytosis", "Lymphohistiocytosis, Familial Hemophagocytic", "Hemophagocytic Lymphohistiocytosis Familial 1", "familial hemophagocytic lymphohistiocytosis 1", "Familial Erythrophagocytic Lymphohistiocytosis", "Familial erythrophagocytic lymphohistiocytosis", "Hemophagocytic Lymphohistiocytosis Familial -1", "Familial Erythrophagocytic Lymphohistiocytoses", "Erythrophagocytic lymphohistiocytosis, familial", "Erythrophagocytic Lymphohistiocytoses, Familial", "hemophagocytic lymphohistiocytosis, familial, 1", "Erythrophagocytic Lymphohistiocytosis, Familial", "HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1", "familial hemophagocytic reticulosis (diagnosis)", "ERYTHROPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL", "Lymphohistiocytoses, Familial Erythrophagocytic", "Hemophagocytic Lymphohistiocytosis, Familial, 1", "Lymphohistiocytosis, Familial Erythrophagocytic", "FHL - Familial hemophagocytic lymphohistiocytosis", "familial hemophagocytic lymphohistiocytosis type 1", "FHL - Familial haemophagocytic lymphohistiocytosis", "FEL - Familial erythrophagocytic lymphohistiocytosis", "Familial hemophagocytic lymphohistiocytosis (disorder)", "familial hemophagocytic lymphohistiocytosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial hemophagocytic lymphohistiocytosis type 1", "shortest_name_length": 3}
{"curie": "UMLS:C0267090", "names": ["Esophageal intramural hematoma", "Intramural esophageal hematoma", "Intramural oesophageal haematoma", "Oesophageal intramural haematoma", "Intramural esophageal hematoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intramural esophageal hematoma", "shortest_name_length": 30}
{"curie": "UMLS:C1167718", "names": ["Hepatic cancer stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatic cancer stage II", "shortest_name_length": 23}
{"curie": "MONDO:0043139", "names": ["Microcephaly sparse hair mental retardation seizures", "microcephaly sparse hair intellectual disability seizures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly sparse hair intellectual disability seizures", "shortest_name_length": 52}
{"curie": "UMLS:C1336464", "names": ["Stage I Peripheral T-cell Lymphoma", "Peripheral T-cell Lymphoma Stage I", "Stage I Mature T- and NK-Cell Lymphoma", "Ann Arbor Stage I Mature T- and NK-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage I Mature T- and NK-Cell Lymphoma", "shortest_name_length": 34}
{"curie": "UMLS:C1697885", "names": ["Left ventricle outflow tract obstruction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Left ventricle outflow tract obstruction", "shortest_name_length": 40}
{"curie": "MONDO:0013758", "names": ["CMTDIE", "Charcot-Marie-Tooth disease - nephropathy", "Charcot-Marie-Tooth disease-nephropathy syndrome", "Charcot-Marie-Tooth disease dominant intermediate E", "CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE E", "Charcot-Marie-Tooth disease, dominant intermediate E", "Charcot-Marie-Tooth disease with nephropathy syndrome", "Charcot-Marie-Tooth disease dominant intermediate type E", "Charcot-Marie-Tooth disease, dominant Intermediate type E", "Autosomal dominant intermediate Charcot-Marie-Tooth disease type E", "autosomal dominant intermediate Charcot-Marie-Tooth disease type E", "Charcot-Marie-Tooth neuropathy with focal segmental glomerulonephritis", "CHARCOT-MARIE-TOOTH NEUROPATHY WITH FOCAL SEGMENTAL GLOMERULONEPHRITIS", "Autosomal dominant intermediate Charcot-Marie-Tooth disease type E (disorder)", "Autosomal dominant intermediate Charcot-Marie-Tooth disease type E (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease dominant intermediate E", "shortest_name_length": 6}
{"curie": "MONDO:0033362", "names": ["DEE53", "EIEE53", "early infantile epileptic encephalopathy 53", "epileptic encephalopathy, early infantile, 53", "developmental and epileptic encephalopathy 53", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 53", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 53", "developmental and epileptic encephalopathy, 53"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 53", "shortest_name_length": 5}
{"curie": "MONDO:0021548", "names": ["CCT", "cataract, total congenital", "total early-onset cataract", "cataract, total congenital with posterior sutural opacities in heterozygotes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "total early-onset cataract", "shortest_name_length": 3}
{"curie": "UMLS:C0279730", "names": ["glucagon secreting adenoma", "glucagon producing adenoma", "adenoma, glucagon secreting", "adenoma, glucagon producing", "pancreas; alpha cell adenoma", "adenoma; alpha cell, pancreas", "pancreas; adenoma, alpha cell", "Pancreatic Alpha Cell Adenoma", "pancreatic alpha cell adenoma", "alpha cell; adenoma, pancreas", "adenoma, pancreatic alpha cell", "adenoma, alpha cell, pancreatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Alpha Cell Adenoma", "shortest_name_length": 26}
{"curie": "MONDO:0011823", "names": ["DJO", "Juvenile-onset dystonia", "juvenile-onset dystonia", "dystonia, juvenile-onset", "Dystonia, juvenile-onset", "DYSTONIA, JUVENILE-ONSET", "developmental malformations-deafness-dystonia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental malformations-deafness-dystonia syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C0278834", "names": ["Prostate cancer stage I", "Stage I Prostate Cancer", "stage I prostate cancer", "Prostatic cancer stage I", "prostate cancer, stage I", "Stage I Prostate Carcinoma", "stage I cancer of the prostate", "Prostate Cancer Stage I AJCC v6", "Stage I Prostate Cancer AJCC v6", "cancer of the prostate, stage I", "Stage I Prostatic Cancer AJCC v6", "Carcinoma of the prostate stage I", "stage I carcinoma of the prostate", "Prostate Carcinoma Stage I AJCC v6", "Cancer of Prostate Stage I AJCC v6", "Stage I Prostate Carcinoma AJCC v6", "carcinoma of the prostate, stage I", "Stage I Cancer of Prostate AJCC v6", "Stage I Prostatic Carcinoma AJCC v6", "Cancer of the Prostate Stage I AJCC v6", "Stage I Cancer of the Prostate AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Prostate Carcinoma", "shortest_name_length": 23}
{"curie": "MONDO:0011987", "names": ["CORD13", "cone-rod dystrophy 13", "CONE-ROD DYSTROPHY 13", "Cone-Rod Dystrophy 13", "RPGRIP1 cone-rod dystrophy", "cone-rod dystrophy type 13", "cone-rod dystrophy caused by mutation in RPGRIP1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cone-rod dystrophy 13", "shortest_name_length": 6}
{"curie": "MONDO:0004220", "names": ["Sarcomatoid Uterine Corpus Endometrioid Adenocarcinoma", "sarcomatoid uterine corpus endometrioid adenocarcinoma", "Endometrial Endometrioid Adenocarcinoma with Spindled Epithelial Cells", "endometrial endometrioid adenocarcinoma with spindled epithelial cells"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometrial endometrioid adenocarcinoma with spindled epithelial cells", "shortest_name_length": 54}
{"curie": "MONDO:0033615", "names": ["COQ10D9", "primary coenzyme Q10 deficiency 9", "COENZYME Q10 DEFICIENCY, PRIMARY, 9", "coenzyme q10 deficiency, primary, 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coenzyme q10 deficiency, primary, 9", "shortest_name_length": 7}
{"curie": "MONDO:0800038", "names": ["MTND1 MELAS syndrome", "MELAS syndrome caused by mutation in MTND1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MELAS syndrome caused by mutation in MTND1", "shortest_name_length": 20}
{"curie": "MONDO:0008864", "names": ["BS2", "Biemond syndrome 2", "BIEMOND syndrome II", "BIEMOND SYNDROME II", "Biemond syndrome II", "Biemond syndrome type 2", "Biemond syndrome, type 2", "Biemond syndrome type 2 (disorder)", "Biemond syndrome, type 2 (diagnosis)", "hypogonadism-short stature-coloboma-preaxial polydactyly syndrome", "Hypogonadism-short stature-coloboma-preaxial polydactyly syndrome", "iris coloboma, mental retardation, obesity, hypogenitalism, and postaxial polydactyly", "iris coloboma, intellectual disability, obesity, hypogenitalism, and postaxial polydactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Biemond syndrome type 2", "shortest_name_length": 3}
{"curie": "UMLS:C0271543", "names": ["Pituitary Abscess", "pituitary abscess", "pituitary; abscess", "abscess; pituitary", "Abscess of pituitary", "pituitary abscess (diagnosis)", "Abscess of pituitary (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abscess of pituitary", "shortest_name_length": 17}
{"curie": "MONDO:0041295", "names": ["PAPILLARY NECROSIS ACUTE", "papillary necrosis acute", "acute papillary necrosis", "Acute papillary necrosis", "acute necrotizing papillitis", "Acute necrotising papillitis", "Acute necrotizing papillitis", "acute renal medullary necrosis", "Acute renal medullary necrosis", "acute kidney papillary necrosis", "kidney papillary necrosis, acute", "Acute papillary necrosis (disorder)", "Acute papillary necrosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute papillary necrosis", "shortest_name_length": 24}
{"curie": "UMLS:C0559938", "names": ["Perforation ileal", "Ileal perforation", "Ileal Perforation", "PERFORATION ILEAL", "ileum; perforation", "perforation; ileum", "Perforation of ileum", "Perforation of Ileum", "perforation of ileum", "Perforation of ileum (disorder)", "perforation of ileum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perforation of ileum", "shortest_name_length": 17}
{"curie": "MONDO:0014118", "names": ["SCN5", "VPS45 deficiency", "vps45 deficiency", "SCN 5-Autosomal Recessive", "severe congenital neutropenia 5", "NEUTROPENIA, SEVERE CONGENITAL, 5, AUTOSOMAL RECESSIVE", "neutropenia, severe congenital, 5, autosomal recessive", "Neutropenia, Severe Congenital, 5, Autosomal Recessive", "Severe Congenital Neutropenia Type 5, Autosomal Recessive", "congenital neutropenia-myelofibrosis-nephromegaly syndrome", "congenital neutropenia-bone marrow fibrosis-nephromegaly syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital neutropenia-myelofibrosis-nephromegaly syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0012487", "names": ["APMR2", "AMR syndrome 2", "Alopecia-Mental Retardation Syndrome 2", "ALOPECIA-MENTAL RETARDATION SYNDROME 2", "alopecia-mental retardation syndrome 2", "alopecia intellectual disability syndrome 2", "ALOPECIA-INTELLECTUAL DISABILITY SYNDROME 2", "alopecia-intellectual disability syndrome 2", "alopecia with mild to moderate intellectual deficit"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alopecia-intellectual disability syndrome 2", "shortest_name_length": 5}
{"curie": "MONDO:0011477", "names": ["STHAG3", "PAX9 tooth agenesis", "hypodontia/oligodontia 3", "HYPODONTIA/OLIGODONTIA 3", "Hypodontia-Oligodontia 3", "Tooth Agenesis, Selective, 3", "tooth agenesis, selective, 3", "TOOTH AGENESIS, SELECTIVE, 3", "tooth agenesis, selective, type 3", "tooth agenesis caused by mutation in PAX9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tooth agenesis, selective, 3", "shortest_name_length": 6}
{"curie": "MONDO:0032735", "names": ["CTRCT48", "CATARACT 48", "cataract 48"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 48", "shortest_name_length": 7}
{"curie": "MONDO:0009908", "names": ["HPABH4D", "PCD deficiency", "PCBD DEFICIENCY", "PCBD deficiency", "PCBD Deficiency", "CADH Deficiency", "CADH deficiency", "CADH DEFICIENCY", "PCBD1 deficiency", "dehydratase deficiency", "Deficiency of hydrolyase", "Deficiency of dehydratase", "Deficiency of hydrolyase (disorder)", "BH4-deficient hyperphenylalaninemia D", "HYPERPHENYLALANINEMIA, BH4-DEFICIENT, D", "Hyperphenylalaninemia, BH4-Deficient, D", "hyperphenylalaninemia, BH4-deficient, D", "Hyperphenylalaninemia with primapterinuria", "HYPERPHENYLALANINEMIA WITH PRIMAPTERINURIA", "hyperphenylalaninemia with primapterinuria", "hyperphenylalaninemia, Bh4-deficient, type D", "Hyperphenylalaninemia due to dehydratase deficiency", "hyperphenylalaninemia due to dehydratase deficiency", "pterin-4 alpha-carbinolamine dehydratase deficiency", "Pterin-4 alpha-carbinolamine dehydratase deficiency", "pterin-4 alpha-carbinolamine dehydratase 1 deficiency", "hyperphenylalaninemia due to pterin-4-alpha-carbinolamine dehydratase deficiency", "Hyperphenylalaninemia due to pterin-4-alpha-carbinolamine dehydratase deficiency", "HYPERPHENYLALANINEMIA, TETRAHYDROBIOPTERIN-DEFICIENT, DUE TO PTERIN-4-ALPHA-CARBINOLAMINE DEHYDRATASE DEFICIENCY", "hyperphenylalaninemia, tetrahydrobiopterin-deficient, due to pterin-4-Alpha-carbinolamine dehydratase deficiency", "Hyperphenylalaninemia, Tetrahydrobiopterin-Deficient, due to Pterin-4-Alpha-Carbinolamine Dehydratase Deficiency", "tetrahydrobiopterin (BH4)-deficient hyperphenylalaninemia (HPA) due to pterin-4-alpha-carbinolamine dehydratase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pterin-4 alpha-carbinolamine dehydratase 1 deficiency", "shortest_name_length": 7}
{"curie": "UMLS:C2349403", "names": ["acute on chronic GVHD", "Acute on Chronic Graft Versus Host Disease", "acute on chronic graft-versus-host disease", "Acute on Chronic Graft-Versus-Host Disease", "Acute on chronic graft-versus-host disease", "graft-versus-host disease (GVHD) acute on chronic", "Acute on chronic graft-versus-host disease (disorder)", "acute on chronic graft-versus-host disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute on chronic graft-versus-host disease", "shortest_name_length": 21}
{"curie": "MONDO:0030726", "names": ["SCN9", "NEUTROPENIA, SEVERE CONGENITAL, 9, AUTOSOMAL DOMINANT", "neutropenia, severe congenital, 9, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neutropenia, severe congenital, 9, autosomal dominant", "shortest_name_length": 4}
{"curie": "UMLS:C0155967", "names": ["Bleeding acute gastric ulcer", "Acute gastric ulcer with bleeding", "acute gastric ulcer with hemorrhage", "Acute gastric ulcer with hemorrhage", "Acute gastric ulcer with haemorrhage", "Gastric ulcer, acute with hemorrhage", "Gastric ulcer, acute with haemorrhage", "ulcer; gastric, acute, with hemorrhage", "stomach; ulcer, acute, with hemorrhage", "Acute gastric ulcer with hemorrhage (disorder)", "acute gastric ulcer with hemorrhage (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute gastric ulcer with hemorrhage", "shortest_name_length": 28}
{"curie": "MONDO:0007457", "names": ["Diastema, Dental Medial", "DIASTEMA, DENTAL MEDIAL", "diastema, dental medial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diastema, dental medial", "shortest_name_length": 23}
{"curie": "MONDO:0004436", "names": ["ovary myxoid liposarcoma", "Ovarian Myxoid Liposarcoma", "ovarian myxoid liposarcoma", "Myxoid Liposarcoma of Ovary", "myxoid liposarcoma of ovary", "myxoid liposarcoma of the ovary", "Myxoid Liposarcoma of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian myxoid liposarcoma", "shortest_name_length": 24}
{"curie": "UMLS:C4744376", "names": ["Sellar Dedifferentiated Chordoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sellar Dedifferentiated Chordoma", "shortest_name_length": 32}
{"curie": "UMLS:C3900115", "names": ["Acute cellular allograft nephropathy", "Acute Cellular Allograft Nephropathy", "Acute Cellular Kidney Allograft Nephropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute cellular allograft nephropathy", "shortest_name_length": 36}
{"curie": "MONDO:0005338", "names": ["POAG", "GLC1D", "GLC1H", "GLC1F", "GLC1I", "GLC1E", "GLC1B", "GLC1G", "glaucoma simple", "Simple Glaucoma", "Glaucoma simplex", "glaucoma simplex", "simple; glaucoma", "Glaucoma, Simple", "Glaucoma Simplex", "glaucoma; simple", "simplex glaucoma", "Donder's glaucoma", "Simplex, Glaucoma", "Donders' glaucoma", "wide-angle glaucoma", "open angle glaucoma", "GLAUCOMA OPEN ANGLE", "Open-Angle Glaucoma", "pigmentary glaucoma", "Pigmentary Glaucoma", "Open cleft glaucoma", "open-angle glaucoma", "Open-angle glaucoma", "Open Angle Glaucoma", "glaucoma pigmentary", "Simplices, Glaucoma", "Open angle glaucoma", "angle glaucoma open", "glaucoma open-angle", "Pigmentary glaucoma", "Wide-angle glaucoma", "Glaucoma, Open Angle", "Compensated Glaucoma", "Open-Angle Glaucomas", "Open Angle Glaucomas", "glaucoma; open-angle", "Melanocytic glaucoma", "Glaucoma, Pigmentary", "pigmentary; glaucoma", "Glaucoma, Open-Angle", "GLAUCOMA, OPEN ANGLE", "Glaucoma, open-angle", "glaucoma; pigmentary", "Glaucoma, open angle", "Glaucoma, Compensated", "Compensative Glaucoma", "Glaucoma, Compensative", "chronic simple glaucoma", "Wide-angle glaucoma NOS", "GLAUCOMA, NONCONGESTIVE", "Chronic simple glaucoma", "simple chronic glaucoma", "Open angle glaucoma NOS", "noncongestive; glaucoma", "glaucoma; noncongestive", "GLAUCOMA, CHRONIC SIMPLE", "Wide-angle glaucoma, NOS", "Open-angle glaucoma, NOS", "GLAUCOMA 1, OPEN ANGLE, H", "Glaucoma 1, Open Angle, G", "GLAUCOMA 1, OPEN ANGLE, D", "GLAUCOMA 1, OPEN ANGLE, B", "GLAUCOMA 1, OPEN ANGLE, F", "Glaucoma 1, Open Angle, H", "Glaucoma 1, Open Angle, D", "GLAUCOMA 1, OPEN ANGLE, G", "GLAUCOMA 1, OPEN ANGLE, E", "Glaucoma 1, Open Angle, E", "Glaucoma 1, Open Angle, F", "OAG - Open-angle glaucoma", "Glaucoma 1, Open Angle, I", "GLAUCOMA 1, OPEN ANGLE, I", "chronic; glaucoma, simple", "glaucoma; chronic, simple", "primary open-angle glaucoma", "Primary Open Angle Glaucoma", "primary open angle glaucoma", "Primary open-angle glaucoma", "Primary open angle glaucoma", "glaucoma open-angle primary", "Glaucoma, Primary Open Angle", "GLAUCOMA, PRIMARY OPEN ANGLE", "Advanced open-angle glaucoma", "glaucoma open-angle advanced", "glaucoma, primary open angle", "Glaucoma, open angle, primary", "CSG - Chronic simple glaucoma", "Pigmentary open-angle glaucoma", "pigmentary open-angle glaucoma", "Open-angle glaucoma (disorder)", "Pigmentary glaucoma (disorder)", "Unspecified open-angle glaucoma", "open-angle glaucoma (diagnosis)", "pigmentary glaucoma (diagnosis)", "Glaucoma, open angle, pigmentary", "Open-angle glaucoma, unspecified", "COAG - Chronic open-angle glaucoma", "POAG - Primary open-angle glaucoma", "Chronic Primary Open Angle Glaucoma", "GLAUCOMA 1, OPEN ANGLE, H (disorder)", "GLAUCOMA 1, OPEN ANGLE, D (disorder)", "GLAUCOMA 1, OPEN ANGLE, F (disorder)", "Primary open angle glaucoma (disorder)", "Advanced open-angle glaucoma (disorder)", "[OBSOLETE] Glaucoma, Primary Open Angle", "primary open-angle glaucoma (diagnosis)", "Advanced open-angle glaucoma (diagnosis)", "secondary pigmentary open-angle glaucoma", "GLAUCOMA, PRIMARY OPEN ANGLE, ADULT-ONSET", "pigmentary open-angle glaucoma (diagnosis)", "Secondary open-angle glaucoma with pigment dispersion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "open-angle glaucoma", "shortest_name_length": 4}
{"curie": "MONDO:0018483", "names": ["SPAP", "secondary PAP", "Secondary PAP", "secondary pulmonary alveolar proteinosis", "Secondary pulmonary alveolar proteinosis", "Secondary pulmonary alveolar proteinosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary pulmonary alveolar proteinosis", "shortest_name_length": 4}
{"curie": "MONDO:0003501", "names": ["external Ear epidermoid carcinoma", "External Ear Epidermoid Carcinoma", "epidermoid carcinoma of external Ear", "Epidermoid Carcinoma of External Ear", "external ear squamous cell carcinoma", "External Ear Squamous Cell Carcinoma", "external Ear squamous cell carcinoma", "squamous cell carcinoma of external ear", "squamous cell carcinoma of external Ear", "Squamous Cell Carcinoma of External Ear", "Epidermoid carcinoma of the External ear", "Epidermoid Carcinoma of the External Ear", "epidermoid carcinoma of the external ear", "epidermoid carcinoma of the external Ear", "Squamous Cell Carcinoma of the External Ear", "squamous cell carcinoma of the external Ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "external ear squamous cell carcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C0234300", "names": ["Primary bitter taste disorder", "Taste Disorder, Primary, Bitter", "Taste disorder, primary, bitter", "Primary bitter taste disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Taste Disorder, Primary, Bitter", "shortest_name_length": 29}
{"curie": "MONDO:0010079", "names": ["Canavan", "Asp deficiency", "ASP DEFICIENCY", "Canavan Disease", "Canavan disease", "Acy2 deficiency", "ASPA DEFICIENCY", "CANAVAN DISEASE", "ACY2 deficiency", "Aspa deficiency", "ACY2 DEFICIENCY", "canavan disease", "canavans disease", "Disease, Canavan", "Canavan's disease", "canavan's disease", "Spongiform Leukodystrophy", "aspartoacylase deficiency", "Spongiform leucodystrophy", "Aminoacylase 2 deficiency", "Aspartoacylase deficiency", "ASPARTOACYLASE DEFICIENCY", "aminoacylase 2 deficiency", "AMINOACYLASE 2 DEFICIENCY", "Leukodystrophy, Spongiform", "Canavan disease (diagnosis)", "Von Bogaert-Bertrand disease", "Von Bogaert Bertrand Disease", "Von Bogaert-Bertrand Disease", "von Bogaert-Bertrand disease", "Disease, Von Bogaert-Bertrand", "Van Bogaert Bertrand Syndrome", "VAN BOGAERT-BERTRAND SYNDROME", "Van Bogaert-Bertrand Syndrome", "Spongy Disease of White Matter", "Syndrome, Van Bogaert-Bertrand", "Spongy Degeneration of Infancy", "Spongy Degeneration of the Brain", "Spongy degeneration of the brain", "spongy degeneration of the brain", "Spongy degeneration of white matter", "BRAIN, FAMILIAL SPONGY DEGENERATION", "Canavan-van Bogaert-Bertrand disease", "Canavan-Van Bogaert-Bertrand disease", "Canavan-van Bogaert-Bertrand Disease", "CANAVAN-VAN BOGAERT-BERTRAND DISEASE", "Canavan van Bogaert Bertrand Disease", "Canavan-VAN Bogaert-Bertrand disease", "Canavan-van-Bogaert-Bertrand disease", "Cavanan-van Bogaert-Bertrand disease", "Disease, Canavan-van Bogaert-Bertrand", "Spongy Disease of Central Nervous System", "spongy Degeneration of central nervous system", "Spongy Degeneration Of Central Nervous System", "SPONGY DEGENERATION OF CENTRAL NERVOUS SYSTEM", "Spongy degeneration of central nervous system", "Spongy Degeneration of Central Nervous System", "spongy degeneration of central nervous system", "Spongy degeneration of white matter in infancy", "Spongy Degeneration of White Matter In Infancy", "Spongy Degeneration of the Central Nervous System", "spongy degeneration of the central nervous system", "FAMILIAL IDIOCY WITH SPONGY DEGNERATION OF NEURAXIS", "Spongy degeneration of central nervous system (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Canavan disease", "shortest_name_length": 7}
{"curie": "MONDO:0024291", "names": ["Vascular anomaly", "vascular anomaly", "Anomaly vascular", "anomaly; vascular", "vascular; anomaly", "Vascular anomalies", "anomalies vascular", "Vascular anomaly NOS", "vascular malformation", "malformation vascular", "Vascular Malformation", "Vascular malformation", "malformations vascular", "Vascular malformations", "Malformation, Vascular", "malformation, vascular", "vascular malformations", "Vascular Malformations", "malformations, vascular", "Malformations, Vascular", "Vascular malformation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vascular malformation", "shortest_name_length": 16}
{"curie": "MONDO:0007313", "names": ["glandular cheilitis", "Glandular cheilitis", "CHEILITIS GLANDULARIS", "Cheilitis glandularis", "cheilitis glandularis", "Cheilitis glandularis, NOS", "Simple cheilitis glandularis", "Cheilitis glandularis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cheilitis glandularis", "shortest_name_length": 19}
{"curie": "MONDO:0018449", "names": ["Cyst-associated renal cell carcinoma", "Acquired cystic disease-associated renal cell carcinoma", "acquired cystic disease-associated renal cell carcinoma", "Acquired Cystic Disease-Associated Renal Cell Carcinoma", "Acquired cystic disease associated renal cell carcinoma", "Acquired cystic disease-associated renal cell carcinoma (RCC)", "Acquired cystic disease associated renal cell carcinoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired cystic disease-associated renal cell carcinoma", "shortest_name_length": 36}
{"curie": "UMLS:C5204291", "names": ["Carcinoma Cuniculatum of the Penis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carcinoma Cuniculatum of the Penis", "shortest_name_length": 34}
{"curie": "MONDO:0002455", "names": ["exocervical cancer", "Exocervical Cancer", "exocervix carcinoma", "Exocervix Carcinoma", "ectocervix carcinoma", "exocervical carcinoma", "Exocervical Carcinoma", "Carcinoma of Exocervix", "Carcinoma of exocervix", "carcinoma of exocervix", "carcinoma of ectocervix", "carcinoma of the Exocervix", "Carcinoma of the Exocervix", "carcinoma of the exocervix", "Carcinoma of exocervix (disorder)", "Carcinoma of exocervix (diagnosis)", "cervical neoplasm malignant exocervix carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exocervical carcinoma", "shortest_name_length": 18}
{"curie": "MONDO:0018953", "names": ["FPP", "PFM", "Catlin Marks", "CATLIN MARKS", "catlin marks", "Catlin marks", "Caitlin marks", "Parietal Foramina", "parietal foramina", "Parietal foramina", "CRANIUM BIFIDUM OCCULTUM", "Cranium Bifidum Occultum", "Cranium bifidum occultum", "Enlarged parietal foramina", "Hereditary cranium bifidum", "enlarged parietal foramina", "Enlarged Parietal Foramina", "hereditary cranium bifidum", "symmetric parietal foramina", "CRANIUM BIFIDUM, HEREDITARY", "Symmetric parietal foramina", "Cranium Bifidum, Hereditary", "foramina parietalia permagna", "Foramina parietalia permagna", "FORAMINA PARIETALIA PERMAGNA", "PARIETAL FORAMINA, SYMMETRIC", "Parietal Foramina, Symmetric", "Foramina Parietalia Permagna", "Fenestrae parietales symmetricae", "fenestrae parietales symmetricae", "Enlarged parietal foramina (disorder)", "Symmetrical, oval parietal bone defects", "Persistent foramina of the parietal bones", "Symmetrical, oval defects in the parietal bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parietal foramina", "shortest_name_length": 3}
{"curie": "UMLS:C0349486", "names": ["Transient Hypothyroxinemia", "Transient hypothyroxinemia", "transient hypothyroxinemia", "transient hypothyroxinaemia", "Transient hypothyroxinaemia", "Transient hypothyroxinemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transient hypothyroxinemia", "shortest_name_length": 26}
{"curie": "MONDO:0015585", "names": ["late-onset infantile spasms", "cryptogenic late-onset epileptic spasms"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cryptogenic late-onset epileptic spasms", "shortest_name_length": 27}
{"curie": "UMLS:C4744988", "names": ["Advanced Small Intestinal Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Small Intestinal Neuroendocrine Carcinoma", "shortest_name_length": 50}
{"curie": "MONDO:0002712", "names": ["epidural space angiolipoma", "angiolipoma of epidural space", "Epidural Spinal Canal Angiolipoma", "epidural spinal canal angiolipoma", "Extradural Spinal canal Angiolipoma", "extradural spinal canal angiolipoma", "angiolipoma of epidural spinal canal", "Angiolipoma of Epidural Spinal Canal", "angiolipoma of extradural spinal canal", "Angiolipoma of Extradural Spinal Canal", "Angiolipoma of Extradural Spinal canal", "angiolipoma of the epidural spinal canal", "Angiolipoma of the Epidural Spinal Canal", "angiolipoma of the extradural spinal canal", "Angiolipoma of the Extradural Spinal Canal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidural spinal canal angiolipoma", "shortest_name_length": 26}
{"curie": "MONDO:0005868", "names": ["myelophthisis", "ANEMIA, MYELOPATHIC", "anemia; myelopathic", "myelopathic; anemia", "myelophthisic anemia", "Myelophthisic Anemia", "Myelophthisic anemia", "MYELOPHTHISIC ANEMIA", "anemias myelophthisic", "Leukoerythroblastosis", "leukoerythroblastosis", "Anemia, Myelophthisic", "myelophthisic; anemia", "Myelophthisic anaemia", "anemia; myelophthisic", "ANEMIA, MYELOPHTHISIC", "LEUKOERYTHROBLASTOSIS", "Myelophthisic Anemias", "Anemias, Myelophthisic", "Leukoerythroblastic anemia", "anemia LEUKOERYTHROBLASTIC", "Leukoerythroblastic Anemia", "Leucoerythroblastic anemia", "ANEMIA LEUKOERYTHROBLASTIC", "Anemia leukoerythroblastic", "leukoerythroblastic anemia", "ANAEMIA LEUKOERYTHROBLASTIC", "Anaemia leukoerythroblastic", "Leukoerythroblastic anaemia", "Anemia, Leukoerythroblastic", "ANEMIA, LEUKOERYTHROBLASTIC", "leukoerythroblastic; anemia", "Leukoerythroblastic Anemias", "anemia, leukoerythroblastic", "Leucoerythroblastic anaemia", "Anemia, leukoerythroblastic", "anemia; leukoerythroblastic", "leukoerythroblastic reaction", "Leukoerythroblastic Reaction", "Anemias, Leukoerythroblastic", "Myelophthisic anemia (disorder)", "myelophthisic anemia (diagnosis)", "leukoerythroblastic anemia (diagnosis)", "Anemia associated with marrow infiltration", "Anaemia associated with marrow infiltration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myelophthisic anemia", "shortest_name_length": 13}
{"curie": "MONDO:0006549", "names": ["Anal tag", "Anal Tag", "anal tag", "tag; anus", "anal tags", "Anal skin tag", "anus skin tag", "anal skin tag", "anal skin tags", "skin tags anal", "Anal skin tags", "skin tag of anus", "anal fibrous polyp", "Anal Fibrous Polyp", "fibrous polyp of anus", "Fibrous Polyp of Anus", "Fibrous polyp of anus", "Anal skin tag (disorder)", "fibrous polyp of the anus", "Fibrous Polyp of the Anus", "anal fibroepithelial polyp", "Anal Fibroepithelial Polyp", "Fibroepithelial polyp of anus", "Fibroepithelial Polyp of Anus", "fibroepithelial polyp of anus", "Fibroepithelial Polyp of the Anus", "fibroepithelial polyp of the anus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibroepithelial polyp of the anus", "shortest_name_length": 8}
{"curie": "MONDO:0003921", "names": ["posterior foramen magnum meningioma", "Posterior Foramen Magnum Meningioma", "Meningioma of Posterior Foramen Magnum", "meningioma of posterior Foramen magnum", "Meningioma of the Posterior Foramen Magnum", "meningioma of the posterior Foramen magnum", "meningioma of the Posterior Foramen Magnum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "posterior foramen magnum meningioma", "shortest_name_length": 35}
{"curie": "MONDO:0018983", "names": ["THS", "Tolosa-Hunt Syndrome", "syndrome tolosa-hunt", "Tolosa Hunt Syndrome", "tolosa hunt syndrome", "Tolosa-Hunt syndrome", "tolosa-hunt syndrome", "Tolosa Hunt syndrome", "Painful ophthalmoplegia", "painful ophthalmoplegia", "PAINFUL OPHTHALMOPLEGIA", "Ophthalmoplegia, painful", "Tolosa-Hunt syndrome (disorder)", "Tolosa-Hunt syndrome (diagnosis)", "Painful ophthalmoplegia (disorder)", "nonspecific inflammation of the cavernous sinus or superior orbital fissure", "Nonspecific inflammation of the cavernous sinus or superior orbital fissure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tolosa-Hunt syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C4764211", "names": ["Advanced Endometrial Carcinosarcoma", "Advanced Uterine Corpus Carcinosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Uterine Corpus Carcinosarcoma", "shortest_name_length": 35}
{"curie": "UMLS:C5444038", "names": ["MBD", "Metastatic Bone Disease", "Symptomatic Bone Disease", "Symptomatic Bone Metastases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Bone Disease", "shortest_name_length": 3}
{"curie": "MONDO:0017553", "names": ["humero-ulnar fusion, bilateral", "humero-ulnar synostosis, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "humero-ulnar synostosis, bilateral", "shortest_name_length": 30}
{"curie": "MONDO:0004641", "names": ["Stage 0 Skin Cancer", "skin cancer stage 0", "Skin Cancer Stage 0", "stage 0 skin cancer", "Skin Carcinoma in situ", "Cancer in situ of skin", "Stage 0 Skin Carcinoma", "Skin Carcinoma Stage 0", "skin carcinoma in situ", "skin carcinoma stage 0", "stage 0 skin carcinoma", "Carcinoma in situ of ear", "carcinoma in situ of ear", "Carcinoma in situ of Skin", "Carcinoma of Skin Stage 0", "carcinoma in situ of skin", "carcinoma of skin stage 0", "Carcinoma in situ of skin", "Cancer in situ skin of lip", "Stage 0 Skin Cancer AJCC v7", "Cutaneous carcinoma in situ", "stage 0 skin cancer aJCC v7", "Stage 0 Skin Cancer AJCC v6", "stage 0 skin cancer aJCC v6", "cutaneous carcinoma in situ", "Cutaneous Carcinoma in situ", "Carcinoma in situ of the Skin", "Carcinoma of the Skin Stage 0", "nonmelanoma carcinoma in situ", "carcinoma in situ of the skin", "carcinoma of the skin stage 0", "stage 0 zone of skin carcinoma", "Carcinoma in situ of skin, NOS", "zone of skin carcinoma in situ", "zone of skin in situ carcinoma", "Carcinoma in situ of skin of lip", "carcinoma in situ of skin of lip", "carcinoma in situ of zone of skin", "Carcinoma in situ of ear (disorder)", "Carcinoma in situ of skin (disorder)", "Cancer in situ of skin of upper limb", "carcinoma in situ of ear (diagnosis)", "carcinoma in situ of skin (diagnosis)", "Carcinoma in situ of skin, unspecified", "Carcinoma in situ of skin of lower limb", "Carcinoma in situ of skin of upper limb", "carcinoma in situ of skin of external ear", "carcinoma in situ of skin of head and neck", "Carcinoma in situ of skin of head and neck", "stage 0 nonmelanoma skin carcinoma in situ", "Carcinoma in situ of skin, site unspecified", "Carcinoma in situ of skin of lip (disorder)", "Carcinoma in situ of scalp and skin of neck", "Carcinoma in situ of skin of scalp and neck", "Carcinoma in situ of skin of upper limb, NOS", "carcinoma in situ of skin of lip (diagnosis)", "Carcinoma in situ of skin of lower limb, NOS", "carcinoma in situ of skin of upper extremities", "carcinoma in situ of skin of lower extremities", "Carcinoma in situ of skin of trunk, excl scrotum", "Carcinoma in situ of skin of lower limb, incl hip", "Carcinoma in situ of skin of lower limb (disorder)", "Carcinoma in situ of skin of upper limb (disorder)", "Carcinoma in situ of skin of trunk, except scrotum", "Carcinoma in situ of skin of trunk, excluding scrotum", "Carcinoma in situ of skin of head and neck (disorder)", "Carcinoma in situ of skin of upper limb, incl shoulder", "Carcinoma in situ of skin of lower limb, including hip", "carcinoma in situ of skin of head and neck (diagnosis)", "Carcinoma in situ of skin of upper limb, including shoulder", "Carcinoma in situ of skin of ear and external auditory canal", "Carcinoma in situ of skin of ear and external auricular canal", "Carcinoma in situ of skin of other and unspecified parts of face", "carcinoma in situ of the skin of the lower limb, including the hip", "carcinoma in situ of the skin of the upper limb, including the shoulder", "carcinoma in situ of the skin of the ear and the external auditory canal", "carcinoma in situ of the skin of the lower limb, including the hip (diagnosis)", "carcinoma in situ of the skin of the upper limb, including the shoulder (diagnosis)", "carcinoma in situ of the skin of the ear and the external auditory canal (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin carcinoma in situ", "shortest_name_length": 19}
{"curie": "MONDO:0013660", "names": ["APUG", "arthrogryposis, Perthes disease, and upward gaze palsy", "ARTHROGRYPOSIS, PERTHES DISEASE, AND UPWARD GAZE PALSY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis, Perthes disease, and upward gaze palsy", "shortest_name_length": 4}
{"curie": "MONDO:0009104", "names": ["FOAR syndrome", "Foar Syndrome", "DBS/FOAR syndrome", "DBS/FOAR SYNDROME", "DBS-FOAR Syndrome", "DONNAI-BARROW SYNDROME", "Donnai-Barrow syndrome", "Donnai Barrow syndrome", "Holmes-Schepens syndrome", "Regenbogen-Donnai syndrome", "faciooculoacousticorenal syndrome", "Faciooculoacousticorenal syndrome", "FACIOOCULOACOUSTICORENAL SYNDROME", "Facio-Oculo-Acoustico-Renal syndrome", "Facio-oculo-acoustico-renal syndrome", "facio-oculo-acoustico-renal syndrome", "facio-oculo-acoustico-renal (FOAR) syndrome", "diaphragmatic hernia-myopia-deafness syndrome", "Diaphragmatic hernia-exomphalos-hypertelorism syndrome", "diaphragmatic hernia-exomphalos-hypertelorism syndrome", "Diaphragmatic hernia-exomphalos-corpus callosum agenesis", "diaphragmatic hernia-exophthalmos-hypertelorism syndrome", "Diaphragmatic Hernia-Exomphalos-Corpus Callosum Agenesis", "Diaphragmatic hernia-hypertelorism-myopia-deafness syndrome", "diaphragmatic hernia-hypertelorism-myopia-deafness syndrome", "Diaphragmatic hernia-hypertelorism-myopia-hearing loss syndrome", "Syndrome of ocular and facial anomalies, telecanthus and deafness", "Diaphragmatic hernia-exomphalos-hypertelorism syndrome (disorder)", "syndrome of ocular and facial anomalies, telecanthus and deafness", "Syndrome of ocular and facial anomalies, telecanthus and hearing loss", "Diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, and sensorineural deafness", "diaphragmatic hernia exomphalos absent corpus callosum hypertelorism myopia sensorineural deafness and proteinuria", "DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM, MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA", "diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, sensorineural deafness, and proteinuria", "diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, sensorineural deafness, and Proteinuria", "Diaphragmatic Hernia, Exomphalos, Absent Corpus Callosum, Hypertelorism, Myopia, Sensorineural Deafness, And Proteinuria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Donnai-Barrow syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0000535", "names": ["tonsil squamous cell carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tonsil squamous cell carcinoma", "shortest_name_length": 30}
{"curie": "UMLS:C4763560", "names": ["Borderline Resectable Pancreatic Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Resectable Pancreatic Carcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0009334", "names": ["HEMOLYTIC ANEMIA WITH THERMAL SENSITIVITY OF RED CELLS", "hemolytic anemia with thermal sensitivity of red cells", "Hemolytic Anemia with Thermal Sensitivity of Red Cells"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemolytic anemia with thermal sensitivity of red cells", "shortest_name_length": 54}
{"curie": "MONDO:0012014", "names": ["CMTRIA", "Ri-Cmta", "RI-CMTA", "RI-CMT type A", "GDAP1 Charcot-Marie-Tooth disease", "Charcot-Marie-Tooth disease recessive intermediate A", "Charcot-Marie-Tooth Disease, Recessive Intermediate A", "Charcot-Marie-Tooth disease, recessive intermediate A", "CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE A", "Charcot-Marie-Tooth disease, recessive intermediate, A", "Charcot-Marie-Tooth disease caused by mutation in GDAP1", "Charcot-Marie-Tooth neuropathy recessive intermediate A", "CHARCOT-MARIE-TOOTH NEUROPATHY, RECESSIVE INTERMEDIATE A", "Charcot-Marie-Tooth Neuropathy, Recessive Intermediate A", "Charcot-Marie-Tooth neuropathy, recessive Intermediate a", "Charcot-Marie-Tooth disease recessive intermediate type A", "Charcot-Marie-Tooth disease, recessive Intermediate type a", "autosomal recessive intermediate Charcot-Marie-Tooth disease type A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease recessive intermediate A", "shortest_name_length": 6}
{"curie": "MONDO:0054695", "names": ["CNM6", "centronuclear myopathy 6 with fiber-type disproportion", "myopathy, centronuclear, 6, with FIBER-type disproportion", "MYOPATHY, CENTRONUCLEAR, 6, WITH FIBER-TYPE DISPROPORTION", "myopathy, centronuclear, 6, with fiber-type disproportion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy, centronuclear, 6, with fiber-type disproportion", "shortest_name_length": 4}
{"curie": "UMLS:C4331474", "names": ["Unresectable Ewing Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Ewing Sarcoma", "shortest_name_length": 26}
{"curie": "UMLS:C4055265", "names": ["Catheter-Related Inflammation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Catheter-Related Inflammation", "shortest_name_length": 29}
{"curie": "UMLS:C0019096", "names": ["American Hemorrhagic Fever", "Fever, American Hemorrhagic", "Hemorrhagic Fever, American"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemorrhagic Fever, American", "shortest_name_length": 26}
{"curie": "UMLS:C4725093", "names": ["Unresectable Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Melanoma", "shortest_name_length": 21}
{"curie": "MONDO:0008153", "names": ["POH", "poh", "Osteodermia", "osteodermia", "Osteomatosis", "Osteoma Cutis", "Osteoma cutis", "OSTEOMA CUTIS", "osteoma cutis", "Osteosis cutis", "osteosis cutis", "Osteosis Cutis", "Miliary osteoma", "Cutaneous osteosis", "Cutaneous Ossification", "Cutaneous ossification", "Osteoma cutis (disorder)", "familial ectopic ossification", "Familial ectopic ossification", "Ectopic Ossification, Familial", "ECTOPIC OSSIFICATION, FAMILIAL", "ectopic ossification, familial", "progressive osseous heteroplasia", "Progressive Osseous Heteroplasia", "Progressive osseous heteroplasia", "Osseous Heteroplasia, Progressive", "OSSEOUS HETEROPLASIA, PROGRESSIVE", "osseous heteroplasia, progressive", "ectopic ossification familial type", "Osteoma cutis (morphologic abnormality)", "Progressive osseous heteroplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive osseous heteroplasia", "shortest_name_length": 3}
{"curie": "MONDO:0019156", "names": ["Servelle-Martorell syndrome", "Servelle Martorell syndrome", "angioosteohypotrophic syndrome", "Angioosteohypotrophic syndrome", "Angio-osteohypotrophic syndrome", "Angio-osteohypotrophic syndrome (disorder)", "Phlebectatic osteohypoplastic angiodysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angioosteohypotrophic syndrome", "shortest_name_length": 27}
{"curie": "UMLS:C5420077", "names": ["Sinonasal Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Non-Hodgkin Lymphoma", "shortest_name_length": 30}
{"curie": "UMLS:C4553250", "names": ["IIA", "Stage IIA Cervical Cancer", "Stage IIA Cervical Cancer AJCC v8", "Stage IIA Cervical Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Cervical Cancer AJCC v8", "shortest_name_length": 3}
{"curie": "UMLS:C0865181", "names": ["Female virilization", "Female Virilization", "Virilization in Girls", "Suprarenal virilization"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Female Virilization", "shortest_name_length": 19}
{"curie": "UMLS:C5206769", "names": ["Refractory Chordoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Chordoma", "shortest_name_length": 19}
{"curie": "UMLS:C4526582", "names": ["Thymus Epithelial Neoplasm by AJCC v8 Stage", "Thymic Epithelial Neoplasm by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thymic Epithelial Neoplasm by AJCC v8 Stage", "shortest_name_length": 43}
{"curie": "UMLS:C2931889", "names": ["Orofaciodigital syndrome 2", "Oral-facial-digital syndrome, type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral-facial-digital syndrome, type 2", "shortest_name_length": 26}
{"curie": "UMLS:C0038368", "names": ["Stomatognathic Disease", "Disease, Stomatognathic", "Stomatognathic Diseases", "Diseases, Stomatognathic", "Mouth and Tooth Diseases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stomatognathic Diseases", "shortest_name_length": 22}
{"curie": "MONDO:0000532", "names": ["lung combined type small cell adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung combined type small cell adenocarcinoma", "shortest_name_length": 44}
{"curie": "UMLS:C1333939", "names": ["Hard Palate Benign Mixed Tumor", "Hard Palate Pleomorphic Adenoma", "Benign Mixed Tumor of Hard Palate", "Pleomorphic Adenoma of Hard Palate", "Benign Mixed Tumor of the Hard Palate", "Pleomorphic Adenoma of the Hard Palate", "Benign Mixed Salivary Tumor of Hard Palate", "Benign Mixed Salivary Tumor of the Hard Palate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hard Palate Pleomorphic Adenoma", "shortest_name_length": 30}
{"curie": "UMLS:C0570328", "names": ["Direct acting anticoagulant adverse reaction", "Direct acting anticoagulant adverse reaction (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Direct acting anticoagulant adverse reaction", "shortest_name_length": 44}
{"curie": "UMLS:C0349744", "names": ["Phobia of exams", "Examination phobia", "Examination Phobia", "examination; phobia", "phobia; examination", "phobia; fear of examination", "Examination phobia (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Examination phobia", "shortest_name_length": 15}
{"curie": "MONDO:0006235", "names": ["GCT", "Abrikosov’s tumor", "Abrikossoff Tumor", "Abrikossoff tumor", "Abrikosov's tumor", "Abrikosoff's tumor", "GRANULAR CELL TUMOR", "Abrikossoff's tumor", "Granular cell tumor", "granular cell tumor", "Granular Cell Tumor", "Abrikossoff's Tumor", "Abrikossoff's tumour", "Granular Cell Tumors", "granular cell tumors", "Granular cell tumour", "cells granular tumor", "granular cell tumour", "Cell Tumor, Granular", "Tumor, Granular Cell", "Tumors, Granular Cell", "Cell Tumors, Granular", "granular cell neoplasm", "Granular cell tumor NOS", "Granular cell tumor, NOS", "Granular Cell Schwannoma", "Granular cell tumour NOS", "granular cell schwannoma", "Granular cell myoblastoma", "neoplasm of granular cell", "Granular cell tumour, NOS", "granular cell myoblastoma", "Granular Cell Myoblastoma", "granular cell myoblastomas", "Cell Myoblastoma, Granular", "Granular Cell Myoblastomas", "Myoblastoma, Granular Cell", "Myoblastomas, Granular Cell", "Cell Myoblastomas, Granular", "malignant granular cell tumor", "Granular cell tumor (disorder)", "Granular cell myoblastoma, NOS", "granular cell tumor (diagnosis)", "Granular Cell Nerve Sheath Tumor", "granular cell nerve sheath tumor", "Abrikosoff's granulous cell tumor", "Malignant variant of Abrikosov's tumor", "malignant variant of Abrikosov's tumor", "giant granulocellular Abrikosov's tumor", "Giant granulo-cellular Abrikosov's tumor", "Granular cell tumor (morphologic abnormality)", "granular cell tumor (morphologic abnormality)", "granular cell tumor NOS (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "granular cell tumor", "shortest_name_length": 3}
{"curie": "UMLS:C0700636", "names": ["FNH", "Hepatic adenoma syndrome", "focal nodal hyperplasia liver", "focal hyperplasia liver nodular", "hepatic focal nodal hyperplasia", "focal nodular hyperplasia liver", "HEPATIC FOCAL NODAL HYPERPLASIA", "hyperplasia; liver, nodular, focal", "Focal Nodular Hyperplasia of Liver", "liver; hyperplasia, nodular, focal", "focal nodular hyperplasia of liver", "Focal nodular hyperplasia of liver", "Focal Nodular Hyperplasia of the Liver", "Focal nodular hyperplasia of liver syndrome", "Focal nodular hyperplasia of liver (disorder)", "focal nodular hyperplasia of liver (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Focal nodular hyperplasia of liver", "shortest_name_length": 3}
{"curie": "MONDO:0009323", "names": ["Halothane hepatitis", "Halothane Hepatitis", "HALOTHANE HEPATITIS", "HEPATITIS, HALOTHANE", "HH - Halothane hepatitis", "Halothane hepatitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Halothane hepatitis", "shortest_name_length": 19}
{"curie": "UMLS:C0432162", "names": ["Spondylolysis, lumbosacral region", "Congenital lumbosacral spondylolysis", "congenital lumbosacral spondylolysis", "Congenital Spondylolysis, Lumbosacral Region", "Spondylolysis, congenital, lumbosacral region", "Congenital spondylolysis of lumbosacral region", "congenital lumbosacral spondylolysis (diagnosis)", "Congenital spondylolysis of lumbosacral region (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital spondylolysis of lumbosacral region", "shortest_name_length": 33}
{"curie": "MONDO:0014256", "names": ["RP67", "RETINITIS PIGMENTOSA 67", "retinitis pigmentosa 67", "NEK2 retinitis pigmentosa", "retinitis pigmentosa type 67", "retinitis pigmentosa caused by mutation in NEK2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 67", "shortest_name_length": 4}
{"curie": "UMLS:C0085617", "names": ["Arteriospasm", "spasm artery", "arteriospasm", "artery spasm", "ARTERIOSPASM", "artery; spasm", "artery spasms", "Arterial spasm", "arterial spasm", "spasm arteries", "ARTERIAL SPASM", "arteries spasms", "spasm; arterial", "Spasm of artery", "arterial spasms", "Arterial spasm NOS", "Spasm of the arteries", "Arteriospasm (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arteriospasm", "shortest_name_length": 12}
{"curie": "UMLS:C4526587", "names": ["Stage III Thymus Epithelial Neoplasm", "Stage III Thymus Epithelial Neoplasm AJCC v8", "Stage III Thymic Epithelial Neoplasm AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Thymic Epithelial Neoplasm AJCC v8", "shortest_name_length": 36}
{"curie": "MONDO:0020096", "names": ["autosomal recessive isolated diffuse palmoplantar keratoderma", "isolated diffuse palmoplantar keratoderma, autosomal recessive", "autosomal recessive isolated diffuse palmoplantar hyperkeratosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive isolated diffuse palmoplantar keratoderma", "shortest_name_length": 61}
{"curie": "UMLS:C0521195", "names": ["Focal Fibrosis", "fibrosis focal", "focal fibrosis", "Focal fibrosis", "Focal fibrosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Focal fibrosis", "shortest_name_length": 14}
{"curie": "MONDO:0017137", "names": ["Robles", "volvulosis", "Onchocercosis", "ONCHOCERCOSIS", "onchocercosis", "Onchocerciasis", "onchocerciasis", "Onchocerciases", "ONCHOCERCIASIS", "River Blindness", "River blindness", "Robles' disease", "infestation; Onchocerca", "Onchocerca; infestation", "onchocerciasis (diagnosis)", "onchocerca volvulus infection", "Onchocerca volvulus infection", "infection by Onchocerca volvulus", "Infection by Onchocerca volvulus", "Infection caused by Onchocerca volvulus", "infection caused by Onchocerca volvulus", "Infection caused by Onchocerca volvulus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "onchocerciasis", "shortest_name_length": 6}
{"curie": "MONDO:0022644", "names": ["Cardiac hydatidosis", "cardiac hydatid cysts with intracavitary expansion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiac hydatid cysts with intracavitary expansion", "shortest_name_length": 19}
{"curie": "MONDO:0009438", "names": ["HYPOURICEMIA, HYPERCALCINURIA, AND DECREASED BONE DENSITY", "Hypouricemia, Hypercalcinuria, and Decreased Bone Density", "hypouricemia, hypercalcinuria, and decreased bone density"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypouricemia, hypercalcinuria, and decreased bone density", "shortest_name_length": 57}
{"curie": "MONDO:0004638", "names": ["Lymphosarcoma", "lymphosarcoma", "LYMPHOSARCOMA", "Lymphosarcomas", "Diffuse lymphoma", "diffuse lymphoma", "lymphoma diffuse", "Diffuse Lymphoma", "Lymphatic Sarcoma", "Lymphosarcoma NOS", "diffuse; lymphoma", "lymphoma; diffuse", "Diffuse Lymphomas", "lymphatic sarcoma", "Lymphoma, Diffuse", "Sarcoma, Lymphatic", "Lymphosarcoma, NOS", "Lymphatic Sarcomas", "Lymphosarcoma, diffuse", "Lymphosarcoma (disorder)", "lymphosarcoma (diagnosis)", "Lymphosarcoma diffuse NOS", "diffuse lymphoma (diagnosis)", "malignant lymphoma (category)", "Reticulolymphosarcoma, diffuse", "Lymphosarcoma type malignant lymphoma", "Malignant lymphoma, lymphosarcoma type", "Lymphosarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphosarcoma", "shortest_name_length": 13}
{"curie": "UMLS:C4527166", "names": ["Stage II Cutaneous (Skin) Melanoma", "Clinical Stage II Cutaneous Melanoma AJCC v8", "Clinical Stage II Melanoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage II Cutaneous Melanoma AJCC v8", "shortest_name_length": 34}
{"curie": "MONDO:0002585", "names": ["proliferative breast lesion", "Proliferative Breast Lesion", "Proliferative Breast Disease", "proliferative breast disease", "Proliferative Fibrocystic Change", "proliferative fibrocystic change", "benign proliferative breast disease", "Benign Proliferative Breast Disease", "proliferating lesion of breast without atypia", "Breast Fibrocystic Change, Proliferative Type", "breast fibrocystic change, proliferative type", "Proliferating Lesion of breast without Atypia", "Proliferative Type Fibrocystic Change of Breast", "proliferative type fibrocystic change of breast", "proliferating lesion of the breast without atypia", "Proliferating Lesion of the breast without Atypia", "Fibrocystic change, proliferative type with atypia", "fibrocystic change, proliferative type with atypia", "Fibrocystic disease, Proliferative type with Atypia", "fibrocystic disease, proliferative type with atypia", "proliferative type fibrocystic change of the breast", "Fibrocystic Disease, Proliferative Type with Atypia", "Fibrocystic disease, proliferative type with atypia", "Proliferative Type Fibrocystic Change of the Breast", "Breast Fibrocystic Change, Proliferative Type with Atypia", "Fibrocystic change, proliferative type with atypia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast fibrocystic change, proliferative type", "shortest_name_length": 27}
{"curie": "MONDO:0002049", "names": ["Low", "low platelet", "platelet low", "thrombopenia", "THROMBOPENIA", "Thrombopenia", "platelets low", "Thrombopenias", "Low platelets", "low platelets", "low; platelets", "platelets; low", "THROMBOCYTOPENIA", "thrombocytopenia", "Thrombocytopenia", "thrombocytopaenia", "Thrombocytopenias", "Thrombocytopaenia", "decreased platelet", "platelet count low", "low platelet count", "Low platelet count", "low count platelet", "Platelet count low", "Low Platelet Count", "platelets decreased", "Platelets decreased", "Decreased platelets", "PLATELETS DECREASED", "decreased platelets", "Thrombocytopenia, NOS", "Decrease in platelets", "reduced platelet count", "Reduced platelet count", "platelet count decreased", "Platelet count decreased", "DECREASED PLATELET COUNT", "Decreased platelet count", "decreased platelet count", "Thrombocytopenic disorder", "thrombocytopenic disorder", "Thrombocytopenic Disorder", "decreased; blood platelets", "blood platelets; decreased", "Thrombocyte count decreased", "thrombocytopenia (diagnosis)", "Thrombocytopenia, unspecified", "Decreased number of platelets", "Platelet count decreased (lab test)", "Thrombocytopenic disorder (disorder)", "Platelet count below reference range", "Platelet count below reference range (finding)", "hematology nonspecific abnormal findings platelet count decreased"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombocytopenia", "shortest_name_length": 3}
{"curie": "MONDO:0021605", "names": ["Benign Eyelid Tumor", "benign eyelid tumor", "eyelid benign neoplasm", "benign eyelid neoplasm", "Benign Tumor of Eyelid", "benign tumor of eyelid", "Benign tumor of eyelid", "Benign Eyelid Neoplasm", "Benign tumour of eyelid", "benign neoplasm of eyelid", "Benign neoplasm of eyelid", "Benign Neoplasm of Eyelid", "benign tumor of the eyelid", "Benign Tumor of the Eyelid", "Benign Neoplasm of the Eyelid", "benign neoplasm of the eyelid", "benign tumor of skin of eyelid", "Benign neoplasm of skin of eyelid", "benign neoplasm of skin of eyelid", "Benign tumor of eyelid (disorder)", "Benign neoplasm of skin of eyelid (disorder)", "benign neoplasm of skin of eyelid (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign eyelid neoplasm", "shortest_name_length": 19}
{"curie": "MONDO:0001793", "names": ["Tearing", "epiphora", "Epiphora", "EPIPHORA", "Epiphoras", "Watery eyes", "Excess tears", "Watering eye", "TEARING EYES", "watering eye", "EYES TEARING", "tearing eyes", "tears; excess", "Epiphora, NOS", "Illacrimation", "excess tearing", "Crocodile tears", "excessive tears", "Increased tears", "excessive; tears", "TEARING EXCESSIVE", "lacrimal disorder", "Tearing increased", "LACRIMAL DISORDER", "Excessive tearing", "excessive tearing", "Excessive Tearing", "Overflow of tears", "Lacrimal disorder", "overflow of tears", "Excessive;tearing", "epiphora (symptom)", "Illacrimation, NOS", "Epiphora (disorder)", "epiphora (diagnosis)", "DISORDER LACRIMATION", "Lacrimation disorder", "LACRIMATION DISORDER", "Unspecified epiphora", "Disorder lacrimation", "Lacrimation increased", "Excessive lacrimation", "Excessive;lacrimation", "Increased lacrimation", "Lacrimation disorders", "excessive lacrimation", "EXCESSIVE LACRIMATION", "increased lacrimation", "Lacrimal disorder NOS", "Lacrimal System Disorder", "Excessive Tear Production", "excessive tear production", "Excessive tear production", "Lacrimal Apparatus Disease", "lacrimal apparatus disease", "Lachrymal system disorders", "Disorder of lacrimal system", "disease, lacrimal apparatus", "epiphora (physical finding)", "Apparatus Disease, Lacrimal", "apparatus disease, lacrimal", "Disease, Lacrimal Apparatus", "Lacrimal Apparatus Disorder", "Lacrimal Apparatus Diseases", "disorder of lacrimal system", "Lacrimal apparatus--Diseases", "Disorders of lacrimal system", "Diseases, Lacrimal Apparatus", "Apparatus Diseases, Lacrimal", "apparatus diseases, lacrimal", "diseases, lacrimal apparatus", "gl.lacrimales; hypersecretion", "hypersecretion; lacrimal glands", "DISORDERS OF THE LACRIMAL SYSTEM", "Disorder of lacrimal system, NOS", "Epiphora, unspecified as to cause", "Excessive tear production (finding)", "Disorder of lacrimal system (disorder)", "disorder of lacrimal system (diagnosis)", "Unspecified disorder of lacrimal system", "Disorder of lacrimal system, unspecified", "disease (or disorder); lacrimal apparatus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "excessive tearing", "shortest_name_length": 7}
{"curie": "MONDO:0005159", "names": ["Prostate cancer", "Prostate Cancer", "prostate cancer", "carcinoma prostate", "prostate carcinoma", "Prostate Carcinoma", "Carcinoma;prostate", "Carcinoma prostate", "Cancer of Prostate", "Prostate carcinoma", "cancer of prostate", "CARCINOMA PROSTATIC", "Carcinoma prostatic", "prostatic carcinoma", "PROSTATE, CARCINOMA", "carcinoma prostatic", "PROSTATIC CARCINOMA", "Prostatic carcinoma", "prostate cancer, NOS", "Prostate cancer, NOS", "carcinoma, prostatic", "Carcinoma of Prostate", "Carcinoma of prostate", "CARCINOMA OF PROSTATE", "carcinoma of prostate", "cancer of the prostate", "Cancer of the Prostate", "prostate gland carcinoma", "Carcinoma of the Prostate", "carcinoma of the prostate", "CA - Carcinoma of prostate", "PROSTATIC CANCER, CARCINOMA", "carcinoma of prostate gland", "Carcinoma of prostate (disorder)", "carcinoma of prostate gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate carcinoma", "shortest_name_length": 15}
{"curie": "UMLS:C0236013", "names": ["HYPEROSMOLAR STATE", "Hyperosmolar state", "hyperosmolar state"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyperosmolar state", "shortest_name_length": 18}
{"curie": "MONDO:0017918", "names": ["Curatolo Cilio Pessagno syndrome", "Curatolo-Cilio-Pessagno syndrome", "White matter hypoplasia, corpus callosum agenesia, and mental retardation", "White matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome", "white matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome", "White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome", "White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome (disorder)", "White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome (diagnosis)", "familial white matter hypoplasia, agenesis of the corpus callosum, intellectual disability and growth deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "white matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome", "shortest_name_length": 32}
{"curie": "MONDO:0017444", "names": ["Hemimelia - knee level", "tibiofibular terminal transverse meromelia", "congenital absence of both lower leg and foot", "Congenital absence of both lower leg and foot", "Transverse deficiency lower limb - knee level", "Transverse deficiency lower limb - knee level (disorder)", "Congenital absence of both lower leg and foot, unspecified lower limb"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital absence of both lower leg and foot", "shortest_name_length": 22}
{"curie": "MONDO:0001641", "names": ["severe edema", "edema severe", "Severe edema", "Severe oedema", "Severe Preeclampsia", "Severe preeclampsia", "severe preeclampsia", "preeclampsia severe", "Severe pre-eclampsia", "severe pre-eclampsia", "Preeclampsia, severe", "pre-eclampsia; severe", "Pre-eclamptic, severe", "Pre-eclampsia, severe", "severe; pre-eclampsia", "Severe pre-eclamptic toxemia", "Severe pre-eclamptic toxaemia", "postpartum severe pre-eclampsia", "Severe pre-eclampsia (disorder)", "antepartum severe pre-eclampsia", "pregnancy; pre-eclampsia, severe", "severe pre-eclampsia (diagnosis)", "Preeclampsia with severe features", "Preeclampsia with Severe Features", "PET - Severe pre-eclamptic toxemia", "Severe pre-eclampsia, with delivery", "severe pre-eclampsia, with delivery", "PET - Severe pre-eclamptic toxaemia", "Severe proteinuric hypertension of pregnancy", "Severe pre-eclampsia, unspecified as to episode of care", "Severe pre-eclampsia, unspecified as to episode of care or not applicable"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe pre-eclampsia", "shortest_name_length": 12}
{"curie": "MONDO:0044916", "names": ["Extrarenal Rhabdoid Tumor", "Extrarenal rhabdoid tumor", "extrarenal rhabdoid tumor", "Extrarenal rhabdoid tumour", "rhabdoid tumor of soft tissue", "Rhabdoid Tumor of Soft Tissue", "Extrarenal rhabdoid tumor (disorder)", "extrarenal rhabdoid tumor (diagnosis)", "Malignant Extrarenal Rhabdoid Neoplasm", "malignant extrarenal rhabdoid neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extrarenal rhabdoid tumor", "shortest_name_length": 25}
{"curie": "MONDO:0018471", "names": ["GEKA", "Grzybowski syndrome", "Eruptive keratoacanthoma", "Eruptive keratoacanthoma (disorder)", "Generalised eruptive keratoacanthoma", "Eruptive keratoacanthoma (diagnosis)", "generalized eruptive keratoacanthoma", "Generalized eruptive keratoacanthoma", "skin neoplasm keratoacanthoma eruptive", "generalized eruptive keratoacanthomas of Grzybowski", "Generalized eruptive keratoacanthomas of Grzybowski"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "generalized eruptive keratoacanthoma", "shortest_name_length": 4}
{"curie": "UMLS:C3274486", "names": ["Sacral Myelocele"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sacral Myelocele", "shortest_name_length": 16}
{"curie": "UMLS:C2827493", "names": ["Non-Trisomic Autosomal Aneuploidy", "Aneuploid Chromosome Number - Non-Trisomic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Trisomic Autosomal Aneuploidy", "shortest_name_length": 33}
{"curie": "MONDO:0017945", "names": ["HCHWA, Piedmont type", "ABetaL34V amyloidosis", "ABetaL34V-related amyloidosis", "ABeta amyloidosis, Piedmont type", "hereditary cerebral hemorrhage with amyloidosis, Piedmont type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ABetaL34V amyloidosis", "shortest_name_length": 20}
{"curie": "MONDO:0010547", "names": ["OPCAX", "SCAX1", "Apak syndrome", "OPCA, X-linked", "OPCA, X-Linked", "OPCA, X-LINKED", "X-linked cerebellar ataxia", "X-linked cerebellar ataxia (CLA)", "X-linked spinocerebellar ataxia 1", "spinocerebellar ataxia, X-linked 1", "SPINOCEREBELLAR ATAXIA, X-LINKED 1", "Spinocerebellar Ataxia, X-Linked 1", "X-linked olivopontocerebellar atrophy", "olivopontocerebellar atrophy, X-linked", "X-linked progressive cerebellar ataxia", "OLIVOPONTOCEREBELLAR ATROPHY, X-LINKED", "Olivopontocerebellar Atrophy, X-Linked", "spinocerebellar ataxia, X-linked type 1", "X-linked olivopontocerebellar atrophy (OPCA)", "spinocerebellar ataxia, X-linked 1, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked progressive cerebellar ataxia", "shortest_name_length": 5}
{"curie": "MONDO:0006447", "names": ["Nonseminomatous germ cell tumor of testis", "nonseminomatous germ cell tumor of testis", "non-seminomatous germ cell tumor of testis", "Non-seminomatous germ cell tumor of testis", "Nonseminomatous germ cell tumour of testis", "Testicular Germ Cell Tumor Non-Seminomatous", "Testicular non seminomatous germ cell tumor", "testicular non seminomatous germ cell tumor", "testicular non-seminomatous germ cell tumor", "testicular germ cell tumor non-seminomatous", "Testicular Non-Seminomatous Germ Cell Tumor", "Non-seminomatous germ cell neoplasm of testis", "non-dysgerminomatous germ cell tumor of testis", "Non-dysgerminomatous germ cell tumor of testis", "Testicular non-dysgerminomatous germ cell tumor", "testicular non-dysgerminomatous germ cell tumor", "nonseminomatous germ cell tumor of testis (diagnosis)", "Non-seminomatous germ cell neoplasm of testis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular non-seminomatous germ cell tumor", "shortest_name_length": 41}
{"curie": "MONDO:0010073", "names": ["Sedt with mental retardation", "SEDT WITH MENTAL RETARDATION", "Sedt with intellectual disability", "Spondyloepiphyseal dysplasia tarda Kohn type", "Spondyloepiphyseal dysplasia tarda, Kohn type", "spondyloepiphyseal dysplasia tarda, Kohn type", "Spondyloepiphyseal dysplasia tarda Kohn type (disorder)", "Spondyloepiphyseal dysplasia tarda Kohn type (diagnosis)", "spondyloepiphyseal dysplasia tarda with mental retardation", "Spondyloepiphyseal Dysplasia Tarda with Mental Retardation", "SPONDYLOEPIPHYSEAL DYSPLASIA TARDA WITH MENTAL RETARDATION", "spondyloepiphyseal dysplasia tarda with intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepiphyseal dysplasia tarda, Kohn type", "shortest_name_length": 28}
{"curie": "MONDO:0019896", "names": ["9qSTDS", "9q subtelomeric deletion syndrome", "Kleefstra syndrome due to del(9)(q34)", "Kleefstra syndrome due to monosomy 9q34", "Kleefstra syndrome due to 9q34 microdeletion", "Kleefstra syndrome due to 9q subtelomeric deletion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kleefstra syndrome due to 9q34 microdeletion", "shortest_name_length": 6}
{"curie": "MONDO:0018233", "names": ["OPSD", "OPD spectrum disorder", "OTOPALATODIGITAL SPECTRUM DISORDER", "Otopalatodigital Spectrum Disorder", "Otopalatodigital spectrum disorder", "fronto-otopalatodigital osteodysplasia", "OPD (otopalatodigital) spectrum disorder", "otopalatodigital syndrome spectrum disorder", "Otopalatodigital syndrome spectrum disorder", "Otopalatodigital syndrome spectrum disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "otopalatodigital syndrome spectrum disorder", "shortest_name_length": 4}
{"curie": "MONDO:0014536", "names": ["THC5", "thrombocytopenia 5", "THROMBOCYTOPENIA 5", "ETV6 thrombocytopenia", "thrombocytopenia type 5", "THROMBOCYTOPENIA, AUTOSOMAL DOMINANT, 5", "thrombocytopenia, autosomal dominant, 5", "thrombocytopenia caused by mutation in ETV6", "thrombocytopenia 5 with increased susceptibility to malignancy", "THROMBOCYTOPENIA 5 WITH INCREASED SUSCEPTIBILITY TO MALIGNANCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombocytopenia 5", "shortest_name_length": 4}
{"curie": "MONDO:0024262", "names": ["Massive aspiration syndrome", "Massive aspiration syndrome, NOS", "aspiration of birth canal contents", "massive neonatal aspiration syndrome", "Neonatal massive aspiration syndrome", "Aspiration of contents of birth canal", "massive aspiration syndrome of newborn", "Massive aspiration syndrome of newborn", "Massive aspiration syndrome (disorder)", "Aspiration of contents of birth canal, NOS", "massive aspiration syndrome of newborn (diagnosis)", "fetal or newborn aspiration of birth canal contents", "fetal or newborn aspiration of birth canal contents (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "massive neonatal aspiration syndrome", "shortest_name_length": 27}
{"curie": "MONDO:0016902", "names": ["partial deletion of chromosome 3q", "partial monosomy of chromosome 3q", "partial monosomy of the long arm of chromosome 3", "partial deletion of the long arm of chromosome 3", "partial deletion of the long arm of chromosome type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of the long arm of chromosome 3", "shortest_name_length": 33}
{"curie": "UMLS:C1519507", "names": ["Stage III High Grade Burkitt-Like Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III High Grade Burkitt-Like Lymphoma", "shortest_name_length": 42}
{"curie": "MONDO:0100148", "names": ["X-linked complex neurodevelopmental disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked complex neurodevelopmental disorder", "shortest_name_length": 44}
{"curie": "UMLS:C4682574", "names": ["Stage IIIC Uterine Corpus Endometrial Stromal Sarcoma", "Stage IIIC Uterine Corpus Endometrial Stromal Sarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Uterine Corpus Endometrial Stromal Sarcoma AJCC v8", "shortest_name_length": 53}
{"curie": "UMLS:C0016171", "names": ["Intestinal Fistula excluding Rectum and Anus", "Fistula of intestine, excluding rectum and anus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fistula of intestine, excluding rectum and anus", "shortest_name_length": 44}
{"curie": "MONDO:0009077", "names": ["DEAFNESS, CONGENITAL, AND FAMILIAL MYOCLONIC EPILEPSY", "deafness, congenital, and familial myoclonic epilepsy", "Deafness, Congenital, and Familial Myoclonic Epilepsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness, congenital, and familial myoclonic epilepsy", "shortest_name_length": 53}
{"curie": "UMLS:C3874358", "names": ["Therapeutic opioid induced constipation", "Therapeutic opioid induced constipation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Therapeutic opioid induced constipation", "shortest_name_length": 39}
{"curie": "UMLS:C1275035", "names": ["PUVA Keratosis", "PUVA keratosis", "Psoralen and long-wave ultraviolet radiation keratosis", "Psoralen and long-wave ultraviolet radiation (PUVA) keratosis", "Psoralen and long-wave ultraviolet radiation keratosis (disorder)", "Psoralen and long-wave ultraviolet radiation keratosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Psoralen and long-wave ultraviolet radiation (PUVA) keratosis", "shortest_name_length": 14}
{"curie": "MONDO:0001406", "names": ["PNS Tumor", "PNS tumor", "PNS neoplasm", "tumor of PNS", "Tumor of PNS", "PNS Neoplasm", "PNS Neoplasms", "PNS neoplasms", "neoplasms, PNS", "Neoplasms, PNS", "Neoplasm of PNS", "neoplasm of PNS", "Tumor of the PNS", "tumor of the PNS", "neoplasm of the PNS", "Neoplasm of the PNS", "nerve sheath tumors", "nerve sheath neoplasm", "peripheral nerve tumor", "Peripheral Nerve Tumor", "Tumor, Peripheral Nerve", "peripheral nerve tumors", "Peripheral Nerve Tumors", "Nerve Tumor, Peripheral", "Nerve Tumors, Peripheral", "Tumors, Peripheral Nerve", "nerves peripheral tumours", "Tumor of Peripheral Nerve", "tumor of peripheral nerve", "Peripheral Nerve Neoplasm", "peripheral nerve neoplasm", "Tumor of peripheral nerve", "nerve neoplasms peripheral", "Neoplasm, Peripheral Nerve", "Nerve Neoplasm, Peripheral", "Peripheral Nerve Neoplasms", "Nerves, Peripheral--Tumors", "Tumour of peripheral nerve", "Neoplasms, Peripheral Nerve", "Nerve Neoplasms, Peripheral", "Neoplasm of Peripheral Nerve", "neoplasm of peripheral nerve", "Neoplasm of peripheral nerve", "tumor of the peripheral nerve", "Tumor of the Peripheral Nerve", "Peripheral Nervous System Tumor", "peripheral nervous system tumor", "neoplasm of the peripheral nerve", "CNS-excluded nervous sys. cancer", "Neoplasm of the Peripheral Nerve", "Tumor of Peripheral Nervous System", "peripheral nervous system neoplasm", "Peripheral nervous system neoplasm", "Peripheral Nervous System Neoplasm", "tumor of peripheral nervous system", "tumour of cranial and spinal nerves", "Peripheral Nervous System Neoplasms", "peripheral nervous system neoplasms", "neoplasms, peripheral nervous system", "Neoplasms, Peripheral Nervous System", "Neoplasm of Peripheral Nervous System", "neoplasm of peripheral nervous system", "tumor of the peripheral nervous system", "Tumor of the peripheral nervous system", "Tumor of the Peripheral Nervous System", "Peripheral nervous system neoplasm NOS", "Neoplasm of peripheral nerve (disorder)", "CNS-excluded nervous system cancer, NOS", "Tumour of the peripheral nervous system", "Neoplasm of the Peripheral Nervous System", "Neoplasm of the peripheral nervous system", "neoplasm of the peripheral nervous system", "peripheral nervous system neoplasm (disease)", "neoplasm of peripheral nervous system (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peripheral nervous system neoplasm", "shortest_name_length": 9}
{"curie": "MONDO:0017928", "names": ["Del(9)(p13)", "monosomy 9p13", "Monosomy 9p13", "9p13 microdeletion syndrome", "9p13 microdeletion syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "9p13 microdeletion syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0013709", "names": ["MRT28", "mental retardation, autosomal recessive 28", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 28", "intellectual disability, autosomal recessive 28", "autosomal recessive intellectual developmental disorder 28", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 28"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 28", "shortest_name_length": 5}
{"curie": "MONDO:0005680", "names": ["Brill", "Zinsser", "Brill disease", "Brill Disease", "Latent typhus", "latent typhus", "BRILL DISEASE", "Brills Disease", "Brill's disease", "Sporadic typhus", "sporadic typhus", "Brill's Disease", "RECRUDESCENT TYPHUS", "recrudescent typhus", "Recrudescent typhus", "TYPHUS, RECRUDESCENT", "Brill-Zinsser disease", "Brill Zinsser Disease", "Brill Zinsser disease", "BRILL-ZINSSER DISEASE", "Brill-Zinsser Disease", "Recrudescent typhus fever", "Brill-Zinsser disease (disorder)", "Brill-Zinsser disease (diagnosis)", "recrudescent [Brill-Zinsser]; typhus", "typhus; recrudescent [Brill-Zinsser]", "Recrudescent typhus [Brill's disease]", "Recrudescent typhus due to Rickettsia prowazekii", "typhus; Rickettsia prowazekii, recrudescent [Brill-Zinsser]", "Rickettsia; prowazekii, typhus, recrudescent [Brill-Zinsser]", "recrudescent [Brill-Zinsser]; typhus, due to Rickettsia prowazekii", "typhus; recrudescent [Brill-Zinsser], due to Rickettsia prowazekii", "prowazekii; Rickettsia prowazekii, typhus, recrudescent [Brill-Zinsser]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brill-Zinsser disease", "shortest_name_length": 5}
{"curie": "UMLS:C4743573", "names": ["Silent Corticotroph Adenoma Type 1", "Nonfunctional Corticotroph Adenoma Type 1", "Densely Granulated Silent Corticotroph Adenoma", "Densely Granulated Nonfunctional Corticotroph Adenoma", "Non-Functioning Densely Granulated Corticotroph Adenoma", "Non-Functioning Densely Granulated  Corticotroph Adenoma", "Non-Functioning Densely Granulated Corticotroph Pituitary Neuroendocrine Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Functioning Densely Granulated Corticotroph Pituitary Neuroendocrine Tumor", "shortest_name_length": 34}
{"curie": "MONDO:0005740", "names": ["Echovirus disease", "Echovirus Infection", "echovirus infection", "Echovirus infection", "Echovirus Infections", "infection, Echovirus", "Echo Virus Infection", "echo Virus infection", "Echo virus infection", "Infection, Echovirus", "Infections, Echovirus", "infection, echo Virus", "Echo Virus Infections", "Infection, Echo Virus", "infections, Echovirus", "echo Virus infections", "Echo viral infections", "Infections, Echo Virus", "infections, echo Virus", "Echovirus infection NOS", "Echo virus infection NOS", "Enterovirus echo infection", "Echovirus disease (disorder)", "Echovirus infectious disease", "echovirus infectious disease", "Echovirus disease or disorder", "echovirus infection (diagnosis)", "Echovirus caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Echovirus infectious disease", "shortest_name_length": 17}
{"curie": "UMLS:C0270408", "names": ["Residual Chronic Schizophrenia", "residual chronic schizophrenia", "chronic residual schizophrenia", "Chronic residual schizophrenia", "Residual schizophrenia, chronic state", "Chronic residual schizophrenia (disorder)", "chronic residual schizophrenia (diagnosis)", "Schizophrenic disorders, residual type, chronic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic residual schizophrenia", "shortest_name_length": 30}
{"curie": "MONDO:0060715", "names": ["HFTC3", "tumoral calcinosis, hyperphosphatemic, familial, 3", "TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 3", "TUMORAL CALCINOSIS, FAMILIAL, HYPERPHOSPHATEMIC, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tumoral calcinosis, hyperphosphatemic, familial, 3", "shortest_name_length": 5}
{"curie": "MONDO:0037003", "names": ["phyllodes malignant tumor", "malignant phyllodes tumor", "Malignant phyllodes tumor", "Malignant Phyllodes Tumor", "phyllodes tumor, malignant", "Malignant phyllodes tumour", "Phyllodes tumor, malignant", "Phyllodes tumour, malignant", "Malignant Phyllodes Neoplasm", "malignant phyllodes neoplasm", "Malignant cystosarcoma phyllodes", "Malignant Cystosarcoma Phyllodes", "malignant cystosarcoma phyllodes", "Cystosarcoma phyllodes, malignant", "Cystosarcoma Phyllodes, Malignant", "Malignant phyllodes tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant phyllodes tumor", "shortest_name_length": 25}
{"curie": "MONDO:0014477", "names": ["DEE26", "EIEE26", "Early Infantile Epileptic Encephalopathy 26", "early infantile epileptic encephalopathy 26", "developmental and epileptic encephalopathy 26", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 26", "epileptic encephalopathy, early infantile, 26", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 26", "Developmental and Epileptic Encephalopathy 26", "KCNB1 early infantile epileptic encephalopathy", "developmental and epileptic encephalopathy, 26", "epileptic encephalopathy, early infantile, type 26", "early infantile epileptic encephalopathy caused by mutation in KCNB1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 26", "shortest_name_length": 5}
{"curie": "UMLS:C1112655", "names": ["peripheral artery occlusion", "Peripheral artery occlusion", "occlusion; artery, peripheral", "peripheral; artery, occlusion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peripheral artery occlusion", "shortest_name_length": 27}
{"curie": "UMLS:C0333416", "names": ["Sperm granuloma", "SPERM GRANULOMA", "sperm granuloma", "Sperm Granuloma", "granuloma sperm", "Spermatogenic granuloma", "Sperm granuloma (disorder)", "Spermatogenic granuloma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sperm granuloma", "shortest_name_length": 15}
{"curie": "UMLS:C0699731", "names": ["hereditary chorea", "Hereditary Chorea", "Hereditary Choreas", "chorea; hereditary", "Chorea, Hereditary", "hereditary; chorea", "Choreas, Hereditary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hereditary Chorea", "shortest_name_length": 17}
{"curie": "UMLS:C1519917", "names": ["Vaginal Blue Nevus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Blue Nevus", "shortest_name_length": 18}
{"curie": "MONDO:0002321", "names": ["Sensory Neuropathy", "Sensory neuropathy", "sensory neuropathy", "NEUROPATHY SENSORY", "neuropathies sensory", "peripheral sensory disorder", "sensory peripheral neuropathy", "PERIPHERAL SENSORY NEUROPATHY", "Sensory neuropathy (disorder)", "peripheral sensory neuropathy", "Peripheral sensory neuropathy", "Sensory peripheral neuropathy", "NEUROPATHY SENSORY PERIPHERAL", "Peripheral Sensory Neuropathy", "peripheral neuropathy sensory", "peripheral Sensory Neuropathy", "Peripheral neuropathy, sensory", "Sensory neuropathy, peripheral", "Sensory peripheral neuropathies", "Damage to nerves that sense feeling", "sensory nerve peripheral neuropathy", "peripheral neuropathy of sensory nerve", "Peripheral sensory neuropathy (disorder)", "Peripheral sensory neuropathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sensory peripheral neuropathy", "shortest_name_length": 18}
{"curie": "UMLS:C4525124", "names": ["Stage III Colon Cancer", "Stage III Colon Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Colon Cancer AJCC v8", "shortest_name_length": 22}
{"curie": "MONDO:0044310", "names": ["DBA17", "DIAMOND-BLACKFAN ANEMIA 17", "Diamond-Blackfan anemia 17", "RPS27-related Diamond-Blackfan anemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diamond-Blackfan anemia 17", "shortest_name_length": 5}
{"curie": "UMLS:C1266026", "names": ["Parietal cell carcinoma", "Parietal cell adenocarcinoma", "Parietal Cell Adenocarcinoma", "Gastric Parietal Cell Adenocarcinoma", "Parietal cell carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parietal cell carcinoma", "shortest_name_length": 23}
{"curie": "UMLS:C1335466", "names": ["Precancerous Condition by Site", "Premalignant Condition by Site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Precancerous Condition by Site", "shortest_name_length": 30}
{"curie": "MONDO:0060596", "names": ["NEDDFL", "NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES", "neurodevelopmental disorder with dysmorphic facies and distal limb anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with dysmorphic facies and distal limb anomalies", "shortest_name_length": 6}
{"curie": "MONDO:0019753", "names": ["Localized Castleman disease", "Localized Castleman Disease", "Localised Castleman disease", "localized Castleman disease", "unicentric Castleman disease", "giant lymph node hyperplasia", "Unicentric Castleman disease", "Castleman disease, unicentric", "angiofollicular lymphoid hyperplasia", "Localized Castleman disease (disorder)", "Unicentric angiofollicular lymph hyperplasia", "localized Angiofollicular lymphoid hyperplasia", "Localized Angiofollicular Lymphoid Hyperplasia", "Unicentric angiofollicular ganglionic hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "localized Castleman disease", "shortest_name_length": 27}
{"curie": "MONDO:0001145", "names": ["Total Third Nerve Palsy", "Total Third-Nerve Palsy", "total third nerve palsy", "Total third nerve palsy", "total third-nerve palsy", "Third-Nerve Palsy, Total", "Palsy, Total Third-Nerve", "Third nerve palsy - total", "Total Third-Nerve Palsies", "Total oculomotor nerve palsy", "total third cranial nerve palsy", "Total third cranial nerve paralysis", "total third nerve palsy (diagnosis)", "third nerve palsy with pupil involved", "Third nerve palsy with pupil involved", "Third or oculomotor nerve palsy, total", "third or oculomotor nerve palsy, total", "Total oculomotor nerve palsy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "total third-nerve palsy", "shortest_name_length": 23}
{"curie": "MONDO:0002016", "names": ["BFNS", "BFIS", "BFIE", "BFNIS", "Benign neonatal epilepsy", "Familial neonatal epilepsy", "familial neonatal seizures", "Familial neonatal seizures", "Familial benign neonatal epilepsy", "Benign Familial Neonatal Epilepsy", "Benign familial neonatal epilepsy", "benign familial neonatal epilepsy", "Familial Benign Neonatal Epilepsy", "Benign familial neonatal seizures", "Benign neonatal-infantile epilepsy", "Benign familial infantile epilepsy", "Benign familial infantile seizures", "Epilepsy, Benign Neonatal, Familial", "Familial Benign Neonatal Convulsions", "Benign neonatal familial convulsions", "Benign familial neonatal convulsions", "Benign Familial Neonatal Convulsions", "Convulsions Benign Familial Neonatal", "Familial neonatal seizures (disorder)", "Benign Familial Infantile Convulsions", "Benign familial infantile convulsions", "Benign Infantile Familial Convulsions", "Convulsions, Benign Neonatal, Familial", "BFIE - benign familial infantile epilepsy", "BFIS - benign familial infantile seizures", "Benign Familial Neonatal Infantile Seizures", "Benign Familial Neonatal-Infantile Seizures", "Benign familial neonatal-infantile seizures", "BFNC - Benign familial neonatal convulsions", "Seizures, Benign Familial Neonatal Infantile", "Seizures, Benign Familial Neonatal-Infantile", "Benign familial infantile epilepsy (disorder)", "Benign Familial Infantile Convulsions Syndrome", "Benign neonatal familial convulsions (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign familial neonatal epilepsy", "shortest_name_length": 4}
{"curie": "UMLS:C3272758", "names": ["Pediatric Viral Disease", "Pediatric Viral Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pediatric Viral Infection", "shortest_name_length": 23}
{"curie": "UMLS:C1336372", "names": ["Stage IVB Hypopharynx Epidermoid Carcinoma", "Stage IVB Hypopharynx Squamous Cell Carcinoma", "Stage IVB Hypopharyngeal Epidermoid Carcinoma", "Stage IVB Epidermoid Carcinoma of Hypopharynx", "Stage IVB Squamous Cell Carcinoma of Hypopharynx", "Stage IVB Hypopharyngeal Squamous Cell Carcinoma", "Stage IVB Epidermoid Carcinoma of the Hypopharynx", "Stage IVB Squamous Cell Carcinoma of the Hypopharynx", "Stage IVB Hypopharyngeal Throat Squamous Cell Cancer", "Stage IVB Hypopharyngeal Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Hypopharyngeal Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 42}
{"curie": "UMLS:C4526719", "names": ["Stage IIA", "Stage IIA Lung Cancer", "Stage IIA Lung Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Lung Cancer AJCC v8", "shortest_name_length": 9}
{"curie": "MONDO:0009383", "names": ["HBLRTFN", "Breastmilk Jaundice", "Breast milk jaundice", "BREAST MILK JAUNDICE", "Breast Milk Jaundice", "breast milk jaundice", "Lucey-Driscoll syndrome", "LUCEY-DRISCOLL SYNDROME", "Breast milk inhibitor jaundice", "jaundice; breast-milk (inhibitor)", "neonatal jaundice from breast milk", "Lucey-Driscoll syndrome (disorder)", "transient familial hyperbilirubinemia", "Neonatal jaundice from breast milk inhibitor", "neonatal jaundice from breast milk (diagnosis)", "transient familial neonatal hyperbilirubinemia", "hyperbilirubinemia transient familial neonatal", "Transient familial neonatal hyperbilirubinemia", "HYPERBILIRUBINEMIA, TRANSIENT FAMILIAL NEONATAL", "hyperbilirubinemia, familial transient neonatal", "Transient familial neonatal hyperbilirubinaemia", "hyperbilirubinemia, transient familial neonatal", "Hyperbilirubinemia, Transient Familial Neonatal", "Hyperbilirubinemia, neonatal, familial, transient", "Breast-feeding inhibitor causing neonatal jaundice", "Breast feeding inhibitors causing neonatal jaundice", "Breast-feeding inhibitors causing neonatal jaundice", "fetal; jaundice, due to or associated with breast milk inhibitors", "Neonatal jaundice due to delayed conjugation from breast milk inhibitor", "Neonatal Jaundice due to Delayed Conjugation from Breast Milk Inhibitors", "Neonatal jaundice due to delayed conjugation from breast milk inhibitors", "Jaundice due to delayed conjugation from causes such as breast milk inhibitors", "Neonatal jaundice due to delayed conjugation from breast milk inhibitor (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transient familial neonatal hyperbilirubinemia", "shortest_name_length": 7}
{"curie": "MONDO:0009412", "names": ["GULOP", "SCURVY", "Scurvy", "scurvy", "scurvies", "Scurvies", "scorbutus", "Scorbutus", "SCORBUTUS", "scorbutic", "hypoascorbemia", "HYPOASCORBEMIA", "Hypoascorbemia", "Hypoascorbemias", "scurvy (diagnosis)", "Gulo, nonfunctional", "GULO, NONFUNCTIONAL", "Gulo, Nonfunctional", "Vitamin C deficiency", "vitamin c deficiency", "vitamin C deficiency", "Vitamin C Deficiency", "Deficiency, Vitamin C", "Vitamin C Deficiencies", "deficiency; vitamin, C", "vitamin; deficiency, C", "deficiency of vitamin c", "Deficiency of vitamin C", "Low levels of vitamin C", "deficiency of vitamin C", "Deficiencies, Vitamin C", "of vitamin c deficiency", "Ascorbic Acid Deficiency", "Ascorbic acid deficiency", "ascorbic acid deficiency", "ASCORBIC ACID DEFICIENCY", "Deficiency, Ascorbic Acid", "ascorbic acid; deficiency", "deficiency; ascorbic acid", "Ascorbic Acid Deficiencies", "Deficiencies, Ascorbic Acid", "Deficiency of ascorbic acid", "Vitamin C deficiency disease", "vitamin C deficiency (diagnosis)", "Ascorbic acid deficiency disease", "L-gulonolactone oxidase pseudogene", "L-GULONOLACTONE OXIDASE PSEUDOGENE", "VITAMIN C, INABILITY TO SYNTHESIZE", "vitamin C, inability to synthesize", "Ascorbic acid deficiency (disorder)", "L-GULONOLACTONE OXIDASE, NONFUNCTIONAL", "L-gulonolactone oxidase, nonfunctional", "L-Gulonolactone Oxidase, Nonfunctional"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scurvy", "shortest_name_length": 5}
{"curie": "MONDO:0017559", "names": ["congenital elbow dislocation, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital elbow dislocation, bilateral", "shortest_name_length": 39}
{"curie": "UMLS:C4744568", "names": ["Metastatic Thyroid Gland Papillary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Thyroid Gland Papillary Carcinoma", "shortest_name_length": 44}
{"curie": "MONDO:0042497", "names": ["mycotoxicosis", "mycotoxicoses", "Mycotoxicoses", "Mycotoxicosis", "poisoning fungi", "Fungi poisoning", "Fungus Poisoning", "Fungal poisoning", "fungus poisoning", "poisoning, fungus", "Poisoning, Fungus", "fungus Poisonings", "Fungus Poisonings", "Poisonings, fungus", "Poisoning by fungi", "Poisonings, Fungus", "Mycotoxicosis, NOS", "Poisoning by fungus", "Fungal poisoning, NOS", "Fungi caused poisoning", "Poisoning by fungus, NOS", "Toxic effect of mycotoxin", "Toxic effect of mycotoxin, NOS", "Toxic effect of mycotoxin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mycotoxicosis", "shortest_name_length": 13}
{"curie": "UMLS:C0276064", "names": ["Sepsis caused by Bacteroides", "Septicemia due to Bacteroides", "Septicemia due to bacteroides", "septicemia due to Bacteroides", "Septicaemia due to Bacteroides", "Septicemia caused by Bacteroides", "Septicaemia caused by Bacteroides", "anaerobic septicemia due to Bacteroides", "Sepsis caused by Bacteroides (disorder)", "septicemia due to Bacteroides (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sepsis caused by Bacteroides", "shortest_name_length": 28}
{"curie": "UMLS:C0851883", "names": ["Neisseria infection", "Neisseria infections", "Neisseria infection NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neisseria infection", "shortest_name_length": 19}
{"curie": "UMLS:C0854941", "names": ["Stage I Ovarian Choriocarcinoma", "Stage I Ovarian Choriocarcinoma AJCC v6", "Stage I Ovarian Choriocarcinoma AJCC v7", "Stage I Ovarian Germ Cell Choriocarcinoma", "Ovarian germ cell choriocarcinoma stage I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian germ cell choriocarcinoma stage I", "shortest_name_length": 31}
{"curie": "UMLS:C5557163", "names": ["Stage IB3 Cervical Cancer AJCC v9", "Stage IB3 Cervical Carcinoma AJCC v9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB3 Cervical Cancer AJCC v9", "shortest_name_length": 33}
{"curie": "UMLS:C0018074", "names": ["Gonococcal infection of lower genitourinary tract", "gonococcal infections of lower genitourinary tract", "Acute gonococcal infection of lower genitourinary tract", "Acute Gonococcal Infection of Lower Genitourinary Tract", "acute gonococcal infections of lower genitourinary tract", "Gonococcal infection (acute) of lower genitourinary tract", "gonococcal infections of lower genitourinary tract (diagnosis)", "acute gonococcal infections of lower genitourinary tract (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute gonococcal infection of lower genitourinary tract", "shortest_name_length": 49}
{"curie": "MONDO:0033044", "names": ["MKS13", "JBTS29", "MECKEL SYNDROME 13", "Meckel syndrome 13", "JOUBERT SYNDROME 29", "Joubert syndrome 29", "Meckel syndrome, type 13"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meckel syndrome 13", "shortest_name_length": 5}
{"curie": "UMLS:C4525396", "names": ["Distal Bile Duct Cancer by AJCC v8 Stage", "Distal Bile Duct Carcinoma by AJCC v8 Stage", "Distal Bile Duct Cancer Tumor Stage (Pathologic)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Distal Bile Duct Cancer by AJCC v8 Stage", "shortest_name_length": 40}
{"curie": "UMLS:C3203574", "names": ["Epstein-Barr virus associated lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epstein-Barr virus associated lymphoma", "shortest_name_length": 38}
{"curie": "MONDO:0015158", "names": ["unexplained periodic fever syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "unexplained periodic fever syndrome", "shortest_name_length": 35}
{"curie": "UMLS:C4331900", "names": ["Iatrogenic Central Hypothyroidism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Iatrogenic Central Hypothyroidism", "shortest_name_length": 33}
{"curie": "MONDO:0037740", "names": ["Malignant CNS Soft Tissue Tumor", "malignant CNS soft tissue tumor", "Malignant Soft Tissue Tumor of CNS", "Malignant CNS Soft Tissue Neoplasm", "malignant CNS soft tissue neoplasm", "malignant soft tissue tumor of CNS", "Malignant Soft Tissue Neoplasm of CNS", "malignant soft tissue neoplasm of CNS", "malignant soft tissue tumor of the CNS", "Malignant Soft Tissue Tumor of the CNS", "malignant soft tissue neoplasm of the CNS", "Malignant Soft Tissue Neoplasm of the CNS", "Soft Tissue Cancer of Central Nervous System", "soft tissue cancer of central nervous system", "Soft Tissue Cancer of the Central Nervous System", "soft tissue cancer of the central nervous system", "malignant central nervous system soft tissue tumor", "Malignant Central Nervous System Soft Tissue Tumor", "malignant central nervous system soft tissue neoplasm", "Malignant Soft Tissue Tumor of Central Nervous System", "Malignant Central Nervous System Soft Tissue Neoplasm", "malignant soft tissue tumor of central nervous system", "Malignant Soft Tissue Neoplasm of Central Nervous System", "malignant soft tissue neoplasm of central nervous system", "Malignant Soft Tissue Tumor of the Central Nervous System", "malignant soft tissue tumor of the central nervous system", "Malignant Soft Tissue Neoplasm of the Central Nervous System", "malignant soft tissue neoplasm of the central nervous system", "malignant central nervous system mesenchymal non-meningothelial tumor", "malignant central nervous system mesenchymal, non-meningothelial tumor", "Malignant Central Nervous System Mesenchymal, Non-Meningothelial Tumor", "central nervous system mesenchymal non-meningothelial tumor, malignant", "malignant central nervous system mesenchymal, non-meningothelial neoplasm", "Malignant Central Nervous System Mesenchymal, Non-Meningothelial Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant central nervous system mesenchymal, non-meningothelial neoplasm", "shortest_name_length": 31}
{"curie": "MONDO:0011271", "names": ["RSS", "RSMD1", "MDRS1", "classic MmD", "Rigid spine syndrome", "rigid spine syndrome", "Rigid Spine Syndrome", "RIGID SPINE SYNDROME", "SEPN1-related myopathy", "MYOPATHY, SEPN1-RELATED", "Myopathy, Sepn1-Related", "myopathy, SEPN1-related", "SELENON rigid spine syndrome", "classic multiminicore disease", "classic multiminicore myopathy", "Rigid Spine Muscular Dystrophy 1", "RIGID SPINE MUSCULAR DYSTROPHY 1", "rigid spine muscular dystrophy 1", "Rigid spine muscular dystrophy-1", "muscular dystrophy, rigid spine, 1", "early-onset desmin-related myopathy", "severe classic form minicore myopathy", "rigid spine muscular dystrophy type 1", "MINICORE MYOPATHY, SEVERE CLASSIC FORM", "severe classic form multicore myopathy", "minicore myopathy, severe classic form", "Minicore myopathy, severe classic form", "multicore myopathy, severe classic form", "MULTICORE MYOPATHY, SEVERE CLASSIC FORM", "Multicore myopathy, severe classic form", "Rigid spine congenital muscular dystrophy", "severe classic form multiminicore disease", "MULTIMINICORE DISEASE, SEVERE CLASSIC FORM", "Multiminicore disease, severe classic form", "multiminicore disease, severe classic form", "desmin-related myopathy with Mallory bodies", "Desmin-Related Myopathy With Mallory Bodies", "DESMIN-RELATED MYOPATHY WITH MALLORY BODIES", "Eichsfeld type congenital muscular dystrophy", "Desmin-related myopathies with Mallory bodies", "MUSCULAR DYSTROPHY, CONGENITAL, EICHSFELD TYPE", "muscular dystrophy, congenital, Eichsfeld type", "Muscular Dystrophy, Congenital, Eichsfeld Type", "rigid spine syndrome caused by mutation in SELENON", "Eichsfeld type congenital muscular dystrophy (disorder)", "desmin-related myopathy with Mallory body-like inclusions", "congenital merosin-positive muscular dystrophy with early spine rigidity", "Muscular dystrophy, congenital, merosin positive with early spine rigidity", "muscular dystrophy, congenital, merosin-positive, with early spine rigidity", "Muscular Dystrophy, Congenital, Merosin-Positive, With Early Spine Rigidity", "MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE, WITH EARLY SPINE RIGIDITY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rigid spine muscular dystrophy 1", "shortest_name_length": 3}
{"curie": "MONDO:0009537", "names": ["LIP", "Lymphoid interstitial pneumonia", "LYMPHOID INTERSTITIAL PNEUMONIA", "lymphoid interstitial pneumonia", "Lymphoid Interstitial Pneumonia", "Lymphocytic interst. pneumonitis", "lymphocytic interst. pneumonitis", "interstitial lymphoid pneumonitis", "Lymphoid interstitial pneumonitis", "Lymphocytic Interstitial Pneumonia", "lymphocytic interstitial pneumonia", "Lymphocytic interstitial pneumonia", "Lymphoid interstitial pneumonia NOS", "Lymphocytic Interstitial Pneumonitis", "Lymphocytic interstitial pneumonitis", "lymphocytic interstitial pneumonitis", "LIP - Lymphoid interstitial pneumonitis", "Lymphoid interstitial pneumonia (disorder)", "lymphoid interstitial pneumonia (diagnosis)", "Idiopathic lymphocytic interstitial pneumonia", "Diffuse Hyperplasia of Bronchus-Associated Lymphoid Tissue", "diffuse hyperplasia of bronchus-associated lymphoid tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphoid interstitial pneumonia", "shortest_name_length": 3}
{"curie": "MONDO:0022457", "names": ["ankyloblepharon filiforme imperforate anus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ankyloblepharon filiforme imperforate anus", "shortest_name_length": 42}
{"curie": "OMIM:125530", "names": ["DERMAL RIDGES, NELSON SYNDROME", "Dermal Ridges, Nelson Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 30}
{"curie": "OMIM:607447", "names": ["BMIQ4", "OBESITY, SUSCEPTIBILITY TO", "BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 5}
{"curie": "MONDO:0020520", "names": ["PLCH", "Adult PLCH", "pulmonary histiocytosis", "Histiocytosis X of lung", "histiocytosis pulmonary", "PULMONARY HISTIOCYTOSIS", "pulmonary histiocytosis X", "Pulmonary Histiocytosis X", "pulmonary histiocytosis x", "Pulmonary histiocytosis X", "Histiocytosis X, Pulmonary", "eosinophilic granuloma lung", "eosinophilic granuloma lungs", "eosinophilic; granuloma, lung", "lung; granuloma, eosinophilic", "granuloma; lung, eosinophilic", "granuloma; eosinophilic, lung", "Eosinophilic granuloma of lung", "Pulmonary eosinophilic granuloma", "Pulmonary Eosinophilic Granuloma", "pulmonary eosinophilic granuloma", "eosinophilic granuloma pulmonary", "PULMONARY EOSINOPHILIC GRANULOMA", "Isolated histiocytosis X of lung", "Langerhans cell histiocytosis of lung", "pulmonary Langerhans cell histiocytosis", "Pulmonary Langerhans cell histiocytosis", "Pulmonary Langerhans Cell Histiocytosis", "Pulmonary Langerhans Cell Granulomatosis", "Langerhans Cell Granulomatosis, Pulmonary", "Pulmonary eosinophilic granuloma (disorder)", "Pulmonary eosinophilic granuloma (diagnosis)", "Adult pulmonary Langerhans cell histiocytosis", "adult pulmonary Langerhans cell histiocytosis", "Langerhans cell histiocytosis of lung (disorder)", "Langerhans cell histiocytosis, unifocal, pulmonary", "pulmonary Langerhans cell histiocytosis (diagnosis)", "Adult pulmonary Langerhans cell histiocytosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult pulmonary Langerhans cell histiocytosis", "shortest_name_length": 4}
{"curie": "MONDO:0013228", "names": ["SMMD", "SPONDYLO-MEGAEPIPHYSEAL-METAPHYSEAL DYSPLASIA", "spondylo-megaepiphyseal-metaphyseal dysplasia", "Spondylo-Megaepiphyseal-Metaphyseal Dysplasia", "Spondylo-megaepiphyseal-metaphyseal dysplasia", "Spondylo-megaepiphyseal-metaphyseal dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondylo-megaepiphyseal-metaphyseal dysplasia", "shortest_name_length": 4}
{"curie": "UMLS:C5237068", "names": ["Refractory Very High Risk Myelodysplastic Syndrome", "Refractory Very High-Risk Myelodysplastic Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Very High Risk Myelodysplastic Syndrome", "shortest_name_length": 50}
{"curie": "MONDO:0032728", "names": ["CMT2EE", "Charcot-Marie-Tooth disease type 2EE", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2EE", "Charcot-Marie-Tooth Neuropathy, Type 2Ee", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2EE", "Charcot-Marie-Tooth disease, axonal, type 2EE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease, axonal, type 2EE", "shortest_name_length": 6}
{"curie": "UMLS:C3272768", "names": ["Appendix NET G2", "Appendix Neuroendocrine Tumor G2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Appendix Neuroendocrine Tumor G2", "shortest_name_length": 15}
{"curie": "MONDO:0003958", "names": ["pediatric central nervous system immature teratoma", "Childhood Central Nervous System Immature Teratoma", "childhood central nervous system immature teratoma", "central nervous system immature teratoma of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood central nervous system immature teratoma", "shortest_name_length": 50}
{"curie": "UMLS:C5554871", "names": ["EBV-SMT", "EBV-Associated Smooth Muscle Tumor", "EBV-Associated Smooth Muscle Neoplasm", "Epstein-Barr Virus-Associated Smooth Muscle Tumor", "Epstein-Barr Virus-Associated Smooth Muscle Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "EBV-Associated Smooth Muscle Tumor", "shortest_name_length": 7}
{"curie": "MONDO:0009442", "names": ["ichthyosis congenita biliary atresia", "ichthyosis congenita with biliary atresia", "Ichthyosis congenita with biliary atresia", "Ichthyosis Congenita With Biliary Atresia", "ICHTHYOSIS CONGENITA WITH BILIARY ATRESIA", "congenital ichthyosis with biliary atresia", "Ichthyosis congenita with biliary atresia (disorder)", "ichthyosis congenita with biliary atresia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ichthyosis congenita with biliary atresia", "shortest_name_length": 36}
{"curie": "UMLS:C1112318", "names": ["Meconium stain", "meconium stain", "meconium stained", "meconium staining", "Meconium staining", "meconium staining (diagnosis)", "meconium staining (physical finding)", "fetal conditions originating in the perinatal period meconium staining"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meconium staining", "shortest_name_length": 14}
{"curie": "MONDO:0600002", "names": ["hemorrhagic fever", "Hemorrhagic Fever", "haemorrhagic fever"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemorrhagic fever", "shortest_name_length": 17}
{"curie": "MONDO:0040653", "names": ["AROA", "Autosomal recessive ocular albinism", "autosomal recessive ocular albinism", "ocular albinism autosomal recessive", "AROA - Autosomal recessive ocular albinism", "autosomal recessive ocular albinism (disease)", "Autosomal recessive ocular albinism (disorder)", "ocular albinism (disease), autosomal recessive", "ocular albinism autosomal recessive (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive ocular albinism", "shortest_name_length": 4}
{"curie": "MONDO:0004900", "names": ["Peripheral Vertigo", "peripheral vertigo", "Vestibular vertigo", "Peripheral vertigo", "vertigo vestibular", "vestibular vertigo", "Vertigo, Peripheral", "peripheral; vertigo", "vertigo; peripheral", "Peripheral Vertigos", "Vertigos, Peripheral", "Peripheral vertigo NOS", "Peripheral vertigo, NOS", "Other peripheral vertigo", "Peripheral vestibular vertigo", "Peripheral vertigo (disorder)", "peripheral vertigo (diagnosis)", "Peripheral vertigo, unspecified", "Other and unspecified peripheral vertigo", "Other peripheral vertigo, unspecified ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peripheral vertigo", "shortest_name_length": 18}
{"curie": "MONDO:0010843", "names": ["DYX2", "dyslexia, susceptibility to, 2", "DYSLEXIA, SUSCEPTIBILITY TO, 2", "READING DISABILITY, SPECIFIC, 2", "reading disability, specific, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyslexia, susceptibility to, 2", "shortest_name_length": 4}
{"curie": "MONDO:0005812", "names": ["flu", "FLU", "Flu", "flus", "GRIP", "grippe", "Grippe", "influenza", "INFLUENZA", "Influenza", "Human Flu", "Influenzas", "Flu, Human", "influenzas", "FLU SYNDROME", "flu syndrome", "Flu syndrome", "SYNDROME FLU", "Syndrome flu", "Influenza NOS", "Influenza, NOS", "Human Influenza", "Influenza, Human", "Human Influenzas", "Influenzas, Human", "Influenza in Human", "influenza infection", "Influenza in Humans", "Influenza (disorder)", "influenza (diagnosis)", "Orthomyxovirus infection", "Orthomyxovirus Infection", "Orthomyxoviridae disease", "orthomyxovirus infection", "Infection, Orthomyxovirus", "Orthomyxovirus Infections", "Orthomyxoviridae Infection", "Infections, Orthomyxovirus", "Orthomyxoviridae Infections", "Infection, Orthomyxoviridae", "Infections, Orthomyxoviridae", "Orthomyxovirus infection, NOS", "Disease due to Orthomyxoviridae", "DISEASES DUE TO ORTHOMYXOVIRIDAE", "Disease caused by Orthomyxoviridae", "Influenza with other manifestations", "orthomyxoviridae infectious disease", "orthomyxoviridae disease or disorder", "Disease due to Orthomyxoviridae, NOS", "orthomyxoviridae caused disease or disorder", "Influenza with non-respiratory manifestation", "influenza with non-respiratory manifestation", "Disease caused by Orthomyxoviridae (disorder)", "Influenza with non-respiratory manifestation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "influenza", "shortest_name_length": 3}
{"curie": "UMLS:C1566050", "names": ["Icterus gravis neonatorum", "Icterus Gravis Neonatorum", "Severe Jaundice in Newborn", "Severe Jaundice in Neonate", "Icterus gravis of the newborn"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Icterus Gravis Neonatorum", "shortest_name_length": 25}
{"curie": "MONDO:0021250", "names": ["Tonsil Tumor", "tonsil tumor", "Tumor of Tonsil", "tumor of tonsil", "Tumor of tonsil", "Tonsil Neoplasm", "Tonsillar Tumor", "tonsil neoplasm", "tonsillar tumor", "Tumour of tonsil", "Tonsillar Neoplasm", "Neoplasm of Tonsil", "tonsillar neoplasm", "neoplasm of tonsil", "Neoplasm of tonsil", "Tonsillar Neoplasms", "Tumor of the Tonsil", "tonsillar neoplasms", "tumor of the tonsil", "Neoplasm of the Tonsil", "neoplasm of the tonsil", "tonsil neoplasm (disease)", "Neoplasm of palatine tonsil", "neoplasm of palatine tonsil", "Neoplasm of palatine tonsil (disorder)", "neoplasm of palatine tonsil (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tonsil neoplasm", "shortest_name_length": 12}
{"curie": "MONDO:0022103", "names": ["PROSTATITIS CHRONIC", "Chronic prostatitis", "chronic prostatitis", "prostatitis chronic", "Chronic Prostatitis", "prostatitis; chronic", "chronic; prostatitis", "PROSTATITIS, CHRONIC", "Chronic prostatitis (disorder)", "Chronic prostatitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic prostatitis", "shortest_name_length": 19}
{"curie": "MONDO:0017397", "names": ["constitutional dyserythropoietic anemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "constitutional dyserythropoietic anemia", "shortest_name_length": 39}
{"curie": "UMLS:C1334220", "names": ["Intermediate Risk Esophageal GIST", "Intermediate Risk Esophageal Gastrointestinal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intermediate Risk Esophageal Gastrointestinal Stromal Tumor", "shortest_name_length": 33}
{"curie": "UMLS:C1142488", "names": ["Intestinal stoma leak", "intestinal stoma leak", "Intestinal Stoma Leakage", "intestinal stoma leak (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal Stoma Leakage", "shortest_name_length": 21}
{"curie": "UMLS:C0541923", "names": ["Lip edema", "Edema lip", "EDEMA LIP", "lip edema", "Lip oedema", "lip oedema", "Oedema lip", "edema lips", "edema of lip", "Edema of the lips", "edema of lip (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lip edema", "shortest_name_length": 9}
{"curie": "MONDO:0001693", "names": ["Ego-alien sexual orientation", "Egodystonic sexual orientation", "Ego-dystonic sexual orientation", "Ego dystonic sexual orientation", "orientation; sexual egodystonic", "ego-dystonic sexual orientation", "ego-dystonic sexual orientation disorder", "Ego-dystonic sexual orientation (finding)", "disorder; sexual, orientation, egodystonic", "sexual; disorder, orientation, egodystonic", "sexual disorder ego-dystonic sexual orientation", "ego-dystonic sexual orientation disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ego-dystonic sexual orientation", "shortest_name_length": 28}
{"curie": "MONDO:0031013", "names": ["autoimmune optic neuritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune optic neuritis", "shortest_name_length": 25}
{"curie": "MONDO:0010064", "names": ["BEDOUIN SPASTIC ATAXIA SYNDROME", "Mousa Al din Al Nassar syndrome", "Mousa-Al Din-Al Nassar syndrome", "Bedouin spastic ataxia syndrome", "Spastic ataxia and corneal dystrophy", "spastic ataxia-ocular anomalies syndrome", "Spastic ataxia-ocular anomalies syndrome", "spastic ataxia-corneal dystrophy syndrome", "Spastic ataxia-corneal dystrophy syndrome", "Spinocerebellar degeneration co-occurrent with macular corneal dystrophy", "Spinocerebellar degeneration co-occurrent with macular corneal dystrophy (disorder)", "spinocerebellar degeneration with macular corneal dystrophy, congenital cataracts, and myopia", "SPINOCEREBELLAR DEGENERATION WITH MACULAR CORNEAL DYSTROPHY, CONGENITAL CATARACTS, AND MYOPIA", "spastic ataxia, macular corneal dystrophy, congenital cataracts, myopia and vertically oval temporally tilted discs"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic ataxia-corneal dystrophy syndrome", "shortest_name_length": 31}
{"curie": "MONDO:0003822", "names": ["Bladder PUNLMP", "bladder PUNLMP", "non-invasive bladder papillary urothelial neoplasm", "Bladder Non-Invasive Papillary Urothelial Neoplasm", "Non-Invasive Bladder Papillary Urothelial Neoplasm", "bladder papillary neoplasm of low malignant potential", "Bladder Papillary Neoplasm of Low Malignant Potential", "papillary urothelial neoplasm of low malignant potential", "Papillary urothelial neoplasm of low malignant potential", "Papillary transitional cell neoplasm of low malignant potential", "Bladder Papillary Urothelial Neoplasm of Low Malignant Potential", "Bladder Papillary Transitional Cell Neoplasm of Low Malignant Potential", "Papillary transitional cell neoplasm of low malignant potential (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-invasive bladder papillary urothelial neoplasm", "shortest_name_length": 14}
{"curie": "MONDO:0020477", "names": ["progeria-associated arthropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progeria-associated arthropathy", "shortest_name_length": 31}
{"curie": "UMLS:C0233774", "names": ["Somatic hallucination", "somatic hallucination", "Somatic Hallucination", "Somatic Hallucinations", "Hallucination, Somatic", "Hallucinations, Somatic", "Visceral hallucinations", "Cenesthesic hallucination", "Cenaesthesic hallucination", "Somatic hallucination (finding)", "Hallucinations of bodily sensation", "somatic hallucination (physical finding)", "Hallucinations of internal bodily sensation", "Hallucinations of bodily sensation (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hallucinations, Somatic", "shortest_name_length": 21}
{"curie": "UMLS:C1335391", "names": ["Peritoneal and Retroperitoneal Tumor", "Peritoneal and Retroperitoneal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peritoneal and Retroperitoneal Neoplasm", "shortest_name_length": 36}
{"curie": "MONDO:0004618", "names": ["Upper diplegia", "diplegia, upper", "Diplegia, upper", "Diplegia (upper)", "arm; paralysis, both", "paralysis; arm, both", "paralysis of both arms", "diplegia of upper limb", "Diplegia of upper limbs", "diplegia of upper limbs", "unable to move both arms", "Thoracic limb paraparesis", "diplegia upper extremities", "Paralysis of both upper limbs", "paralysis of both arms (symptom)", "Diplegia of upper limbs (disorder)", "diplegia upper extremities (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diplegia of upper limb", "shortest_name_length": 14}
{"curie": "MONDO:0017961", "names": ["46,XX disorder of gonadal development"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XX disorder of gonadal development", "shortest_name_length": 37}
{"curie": "UMLS:C5557174", "names": ["Stage III Cervical Cancer AJCC v9", "Stage III Cervical Carcinoma AJCC v9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Cervical Cancer AJCC v9", "shortest_name_length": 33}
{"curie": "UMLS:C4287846", "names": ["Vulvar Superficial Myofibroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Superficial Myofibroblastoma", "shortest_name_length": 35}
{"curie": "MONDO:0030900", "names": ["IDDPADS", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH PAROXYSMAL DYSKINESIA OR SEIZURES", "intellectual developmental disorder with paroxysmal dyskinesia or seizures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder with paroxysmal dyskinesia or seizures", "shortest_name_length": 7}
{"curie": "UMLS:C1291579", "names": ["Deficiency of enolase", "Alpha-Enolase Deficiency", "Erythrocyte Enolase Deficiency", "Deficiency of enolase (disorder)", "Phosphopyruvate Hydratase Deficiency", "Deficiency of phosphopyruvate hydratase", "Deficiency of 2-phosphoglycerate dehydratase"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Deficiency of enolase", "shortest_name_length": 21}
{"curie": "UMLS:C0677725", "names": ["Recurrent Mantle Cell Lymphoma", "Mantle cell lymphoma recurrent", "recurrent mantle cell lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mantle cell lymphoma recurrent", "shortest_name_length": 30}
{"curie": "UMLS:C1335727", "names": ["Peripheral T-Cell Lymphoma Refractory", "Refractory Peripheral T-cell Lymphoma", "Refractory Mature T- and NK-Cell Lymphoma", "Refractory Mature T-Cell and NK-Cell Non-Hodgkin Lymphoma", "Refractory Mature T-Cell and NK-Cell Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Mature T-Cell and NK-Cell Non-Hodgkin Lymphoma", "shortest_name_length": 37}
{"curie": "UMLS:C0343730", "names": ["perianal wart", "perianal warts", "Perianal warts", "warts perianal", "Perianal warts (disorder)", "Perianal warts (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perianal warts", "shortest_name_length": 13}
{"curie": "MONDO:0003690", "names": ["Anaplastic Ependymoma", "anaplastic ependymoma", "Malignant Adult Ependymoma", "malignant adult ependymoma", "Adult Malignant Ependymoma", "adult malignant ependymoma", "Adult Anaplastic Ependymoma", "adult anaplastic ependymoma", "malignant ependymoma, adult", "ependymoma, adult malignant", "anaplastic ependymoma, adult", "anaplastic ependymoma of adults"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult anaplastic ependymoma", "shortest_name_length": 21}
{"curie": "UMLS:C3272969", "names": ["Anal Inflammatory Cloacogenic Polyp"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anal Inflammatory Cloacogenic Polyp", "shortest_name_length": 35}
{"curie": "UMLS:C1262141", "names": ["Poor quality sleep"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Poor quality sleep", "shortest_name_length": 18}
{"curie": "UMLS:C5556296", "names": ["Recurrent Gangliocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Gangliocytoma", "shortest_name_length": 23}
{"curie": "MONDO:0017798", "names": ["Spigelian hernia-cryptorchidism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spigelian hernia-cryptorchidism syndrome", "shortest_name_length": 40}
{"curie": "MONDO:0001897", "names": ["bilateral hyperactive labyrinth", "Bilateral hyperactive labyrinth", "Hyperactive labyrinth, bilateral", "hyperactive labyrinth, bilateral", "bilateral hyperactive labyrinth (diagnosis)", "Hyperactive bilateral labyrinthine dysfunction", "hyperactive bilateral labyrinthine dysfunction", "Hyperactive bilateral labyrinthine dysfunction (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bilateral hyperactive labyrinth", "shortest_name_length": 31}
{"curie": "UMLS:C1699743", "names": ["Intraoperative Renal Injury", "Intraoperative renal injury", "intraoperative renal injury", "intraoperative renal injury (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraoperative Renal Injury", "shortest_name_length": 27}
{"curie": "UMLS:C5446592", "names": ["Processed Food Allergy", "Allergy, Processed Foods"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Processed Food Allergy", "shortest_name_length": 22}
{"curie": "MONDO:0013086", "names": ["NBLST6", "neuroblastoma, susceptibility to, 6", "NEUROBLASTOMA, SUSCEPTIBILITY TO, 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuroblastoma, susceptibility to, 6", "shortest_name_length": 6}
{"curie": "MONDO:0015022", "names": ["IDDDFP", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS", "intellectual developmental disorder with dysmorphic facies and ptosis", "intellectual developmental disorder with dysmorphic facies and ptosis; IDDDFP"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder with dysmorphic facies and ptosis", "shortest_name_length": 6}
{"curie": "MONDO:0019618", "names": ["Sheehan", "Simmonds", "SHEEHAN SYNDROME", "Simmonds Disease", "Sheehan Syndrome", "Sheehan syndrome", "simmonds disease", "sheehan syndrome", "Simmond's Disease", "simmond's disease", "Syndrome, Sheehan", "simmonds' disease", "Simmond's disease", "sheehans syndrome", "Simmonds' Disease", "Simmonds' disease", "Disease, Simmonds", "Sheehans Syndrome", "Sheehan's Syndrome", "Sheehan's syndrome", "sheehan's syndrome", "sheehans's syndrome", "Syndrome, Sheehan's", "Reye-Sheehan syndrome", "Postpartum hypopituitarism", "postpartum hypopituitarism", "Postpartum Hypopituitarism", "hypopituitarism; postpartum", "postpartum; hypopituitarism", "HYPOPITUITARISM, POSTPARTUM", "Hypopituitarism, Postpartum", "Sheehan's syndrome (disorder)", "postpartum panhypopituitarism", "Postpartum Panhypopituitarism", "postpartum pituitary necrosis", "Postpartum pituitary necrosis", "Sheehan's syndrome (diagnosis)", "Panhypopituitarism, Postpartum", "POSTPARTUM PITUITARY HEMORRHAGE", "Postpartum pituitary infarction", "Postpartum necrosis of pituitary", "Postpartum Pituitary Insufficiency", "Pituitary Insufficiency, Postpartum", "Postpartum panhypopituitary syndrome", "POSTPARTUM PANHYPOPITUITARY SYNDROME", "postpartum panhypopituitary syndrome", "Postpartum hypopituitarism (disorder)", "syndrome; postpartum panhypopituitary", "Ischemic postpartum pituitary necrosis", "Postpartum pituitary necrosis syndrome", "postpartum hypopituitarism (diagnosis)", "Ischaemic postpartum pituitary necrosis", "postpartum; panhypopituitarism, syndrome", "Sheehan's syndrome (postpartum necrosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sheehan syndrome", "shortest_name_length": 7}
{"curie": "MONDO:0011618", "names": ["LIVER FIBROCYSTIC DISEASE AND POLYDACTYLY", "Liver Fibrocystic Disease and Polydactyly", "liver fibrocystic disease and polydactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "liver fibrocystic disease and polydactyly", "shortest_name_length": 41}
{"curie": "MONDO:0010792", "names": ["LIMM", "LIMD", "Lethal infantile mitochondrial disease", "lethal infantile mitochondrial disease", "myopathy mitochondrial lethal infantile", "lethal infantile mitochondrial myopathy", "Lethal infantile mitochondrial myopathy", "MITOCHONDRIAL MYOPATHY, LETHAL, INFANTILE", "mitochondrial myopathy, lethal, infantile", "Myopathy, Mitochondrial, Lethal Infantile", "Lethal infantile mitochondrial myopathy (disorder)", "Lethal infantile mitochondrial myopathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal infantile mitochondrial myopathy", "shortest_name_length": 4}
{"curie": "MONDO:0008384", "names": ["node; rheumatoid", "rheumatoid; node", "Rheumatoid nodule", "rheumatoid nodule", "Rheumatoid Nodule", "rheumatoid nodules", "Nodule, Rheumatoid", "nodule; rheumatoid", "rheumatoid; nodule", "Rheumatoid Nodules", "Nodules, Rheumatoid", "Rheumatoid Nodulosis", "Rheumatoid nodulosis", "Rheumatoid Noduloses", "rheumatoid nodulosis", "RHEUMATOID NODULOSIS", "Rheumatoid nodule, NOS", "Rheumatoid nodule (disorder)", "subcutaneous rheumatoid nodule", "Subcutaneous rheumatoid nodule", "Rheumatoid nodulosis (disorder)", "Subcutaneous rheumatoid nodules", "rheumatoid nodulosis (diagnosis)", "accelerated rheumatoid nodulosis", "Accelerated rheumatoid nodulosis", "Subcutaneous rheumatoid nodule (disorder)", "subcutaneous rheumatoid nodule (diagnosis)", "Rheumatoid nodule (morphologic abnormality)", "Accelerated rheumatoid nodulosis (disorder)", "accelerated rheumatoid nodulosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rheumatoid nodulosis", "shortest_name_length": 16}
{"curie": "MONDO:0008865", "names": ["BCD", "BIETTI CRYSTALLINE DYSTROPHY", "Bietti crystalline dystrophy", "Bietti Crystalline Dystrophy", "Bietti Crystalline Retinopathy", "Bietti's crystalline dystrophy", "Bietti crystalline retinopathy", "Bietti's crystalline retinopathy", "BIETTI CRYSTALLINE CORNEORETINAL DYSTROPHY", "Bietti crystalline corneoretinal dystrophy", "Bietti Crystalline Corneoretinal Dystrophy", "Bietti's crystalline retinopathy (disorder)", "Bietti's crystalline corneoretinal dystrophy", "Bietti's crystalline retinopathy (diagnosis)", "Bietti tapetoretinal Degeneration with marginal corneal dystrophy", "BIETTI TAPETORETINAL DEGENERATION WITH MARGINAL CORNEAL DYSTROPHY", "Bietti tapetoretinal degeneration with marginal corneal dystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bietti crystalline corneoretinal dystrophy", "shortest_name_length": 3}
{"curie": "UMLS:C1850598", "names": ["Leigh Syndrome due to Mitochondrial Complex III Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leigh Syndrome due to Mitochondrial Complex III Deficiency", "shortest_name_length": 58}
{"curie": "MONDO:0000828", "names": ["juvenile-onset Parkinson disease", "juvenile-onset Parkinson's disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile-onset Parkinson disease", "shortest_name_length": 32}
{"curie": "UMLS:C5420229", "names": ["Mild ARDS", "Mild Acute Respiratory Distress Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mild Acute Respiratory Distress Syndrome", "shortest_name_length": 9}
{"curie": "UMLS:C4763989", "names": ["Transport Injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transport Injury", "shortest_name_length": 16}
{"curie": "UMLS:C4744385", "names": ["Sellar Germ Cell Tumor", "Germ Cell Tumor of the Sellar Region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sellar Germ Cell Tumor", "shortest_name_length": 22}
{"curie": "UMLS:C1332485", "names": ["Benign Pediatric Germ Cell Tumor", "Benign Childhood Germ Cell Tumor", "Benign Pediatric Germ Cell Neoplasm", "Benign Childhood Germ Cell Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Childhood Germ Cell Tumor", "shortest_name_length": 32}
{"curie": "MONDO:0013187", "names": ["factor XIIIA deficiency", "Reduced factor XIII, subunit A", "Factor XIII subunit A deficiency", "factor XIII, A subunit, deficiency of", "FACTOR XIII, A SUBUNIT, DEFICIENCY OF", "Factor Xiii, A Subunit, Deficiency Of", "Hereditary factor XIII type II deficiency", "hereditary factor XIII type II deficiency", "hereditary factor XIII A subunit deficiency", "Hereditary factor XIII A subunit deficiency", "hereditary factor XIII alpha subunit deficiency", "Hereditary factor XIII alpha subunit deficiency", "Hereditary factor XIII A subunit deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "factor XIII, A subunit, deficiency of", "shortest_name_length": 23}
{"curie": "UMLS:C0494410", "names": ["Nonorganic Sleep Wake Cycle Disorder", "Nonorganic Sleep Wake Cycle Disorders", "non-organic disorder of sleep-wake schedule", "Nonorganic disorder of the sleep-wake schedule", "Non-organic disorder of the sleep-wake schedule", "non-organic disorder of sleep-wake schedule (diagnosis)", "Non-organic disorder of the sleep-wake schedule (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nonorganic Sleep Wake Cycle Disorders", "shortest_name_length": 36}
{"curie": "MONDO:0019613", "names": ["NFPA", "Silent pituitary adenoma", "Null cell pituitary adenoma", "Pituitary null cell adenoma", "silent pituitary gland adenoma", "Functionless Pituitary Adenoma", "nonfunctioning pituitary tumor", "Non-Functioning PitNET/Adenoma", "Functionless pituitary adenoma", "functionless pituitary adenoma", "Silent Pituitary Gland Adenoma", "non-functioning pituitary tumor", "non-secretory pituitary adenoma", "pituitary tumor, nonfunctioning", "Non-Secretory Pituitary Adenoma", "nonfunctioning pituitary tumors", "Non-functioning pituitary tumor", "nonfunctioning pituitary adenoma", "Non-functioning pituitary tumour", "Non-functional pituitary adenoma", "non-functioning pituitary adenoma", "Functionless Adenoma of Pituitary", "Non-functioning pituitary adenoma", "functionless adenoma of pituitary", "Non-Functioning Pituitary Adenoma", "pituitary adenoma, nonfunctioning", "Non-secretory adenoma of pituitary", "Non-Secretory Adenoma of Pituitary", "non-secretory adenoma of pituitary", "Clinically silent pituitary adenoma", "Hormonally silent pituitary adenoma", "functionless pituitary gland adenoma", "Non-Functioning Adenoma of Pituitary", "Functionless Pituitary Gland Adenoma", "non-functioning adenoma of pituitary", "Non-Functioning Pituitary Gland Tumor", "Functionless Adenoma of the Pituitary", "functionless adenoma of the pituitary", "Non-Secretory Pituitary Gland Adenoma", "non-secretory pituitary gland adenoma", "nonfunctional pituitary gland adenoma", "Nonfunctional Pituitary Gland Adenoma", "Non-Secretory Adenoma of the Pituitary", "non-secretory adenoma of the pituitary", "Nonfunctioning Pituitary Gland Adenoma", "non-functioning pituitary gland adenoma", "Non-Functioning Pituitary Gland Adenoma", "functionless adenoma of pituitary gland", "Functionless Adenoma of Pituitary Gland", "Non-Functioning Adenoma of the Pituitary", "non-secretory adenoma of pituitary gland", "non-functioning adenoma of the pituitary", "Non-Secretory Adenoma of Pituitary Gland", "Non-Functioning neoplasm of the Pituitary", "Functionless pituitary adenoma (disorder)", "Non-Functioning Adenoma of Pituitary Gland", "non-functioning adenoma of pituitary gland", "Functionless Adenoma of the Pituitary Gland", "functionless adenoma of the pituitary gland", "non-secretory adenoma of the pituitary gland", "Non-Secretory Adenoma of the Pituitary Gland", "Non-Secretory adenoma of the Pituitary gland", "pituitary non-secretory (chromophobe) adenoma", "Non-Functioning Adenoma of the Pituitary Gland", "Non-Functioning Pituitary Neuroendocrine Tumor", "non-functioning adenoma of the pituitary gland", "non-secretory adenoma of pituitary gland (diagnosis)", "Null cell pituitary adenoma (morphologic abnormality)", "Non-Functioning Pituitary Neuroendocrine Tumor/Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-functioning pituitary adenoma", "shortest_name_length": 4}
{"curie": "MONDO:0012683", "names": ["PCH6", "Pontocerebellar Hypoplasia Type 6", "pontocerebellar hypoplasia type 6", "Pontocerebellar hypoplasia type 6", "PONTOCEREBELLAR HYPOPLASIA, TYPE 6", "pontocerebellar hypoplasia, type 6", "PCH6 - pontocerebellar hypoplasia type 6", "Congenital pontocerebellar hypoplasia type 6", "RARS2 non-syndromic pontocerebellar hypoplasia", "Congenital pontocerebellar hypoplasia type 6 (disorder)", "non-syndromic pontocerebellar hypoplasia caused by mutation in RARS2", "Fatal infantile encephalopathy with mitochondrial respiratory chain defect", "Fatal infantile encephalopathy with mitochondrial respiratory chain defects", "fatal infantile encephalopathy with mitochondrial respiratory chain defects", "encephalopathy fatal infantile with mitochondrial respiratory chain defects", "ENCEPHALOPATHY, FATAL INFANTILE, WITH MITOCHONDRIAL RESPIRATORY CHAIN DEFECTS", "encephalopathy, fatal infantile, with mitochondrial respiratory chain defects", "Encephalopathy, Fatal Infantile, With Mitochondrial Respiratory Chain Defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pontocerebellar hypoplasia type 6", "shortest_name_length": 4}
{"curie": "MONDO:0008718", "names": ["Morvan", "morvan disease", "MORVAN DISEASE", "Morvan Disease", "Morvan syndrome", "Morvan Diseases", "Morvans Disease", "morvan's disease", "Morvan's disease", "Morvan's Disease", "Morvan's Diseases", "Morvan fibrillary chorea", "Morvan's fibrillary chorea", "Morvan syndrome (disorder)", "Morvan syndrome (diagnosis)", "Limbic encephalitis-neuromyotonia-hyperhidrosis-polyneuropathy syndrome", "limbic encephalitis-neuromyotonia-hyperhidrosis-polyneuropathy syndrome", "Limbic encephalitis, neuromyotonia, hyperhidrosis, polyneuropathy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Morvan syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C0151810", "names": ["DRUG EFFECT LACK OF", "LACK OF DRUG EFFECT", "Lack of drug effect", "Lack of drug action", "Drug effect lack of", "Ineffective drug action", "Lack of drug action (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lack of drug action", "shortest_name_length": 19}
{"curie": "UMLS:C4727432", "names": ["Refractory WHO Grade 3 Glioma", "Refractory WHO Grade III Glioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory WHO Grade 3 Glioma", "shortest_name_length": 29}
{"curie": "UMLS:C2981388", "names": ["Stage IIIA Appendix Cancer", "Stage IIIA Appendix Carcinoma", "Stage IIIA Appendix Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Appendix Carcinoma AJCC v7", "shortest_name_length": 26}
{"curie": "MONDO:0012850", "names": ["NPHLOP1", "hypophosphatemic nephrolithiasis/osteoporosis 1", "nephrolithiasis/osteoporosis, hypophosphatemic, 1", "Nephrolithiasis-Osteoporosis, Hypophosphatemic, 1", "NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 1", "hypophosphatemic nephrolithiasis/osteoporosis type 1", "nephrolithiasis/osteoporosis, hypophosphatemic, type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypophosphatemic nephrolithiasis/osteoporosis 1", "shortest_name_length": 7}
{"curie": "MONDO:0008057", "names": ["CNC1", "name syndrome", "lamb syndrome", "Carney syndrome", "Carney Complex, Type I", "PRKAR1A Carney complex", "Carney Complex, Type 1", "CARNEY COMPLEX, TYPE 1", "Carney complex, type 1", "Carney Myxoma-endocrine Complex", "Carney complex caused by mutation in PRKAR1A", "myxoma, spotty pigmentation, and endocrine overactivity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carney complex, type 1", "shortest_name_length": 4}
{"curie": "UMLS:C1707551", "names": ["Cutaneous Mature B-Cell Neoplasm", "Cutaneous Mature B-Cell Lymphocytic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous Mature B-Cell Neoplasm", "shortest_name_length": 32}
{"curie": "UMLS:C0024232", "names": ["Lymphatic Metastasis", "lymphatic metastasis", "Lymphatic metastasis", "Lymphatic Metastases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphatic Metastasis", "shortest_name_length": 20}
{"curie": "MONDO:0004613", "names": ["ischemia; bowel, acute", "acute intestinal ischemia", "Acute intestinal ischemia", "acute mesenteric ischemia", "acute intestinal Ischemia", "ACUTE MESENTERIC ISCHEMIA", "Acute Intestinal Ischemia", "acute ischemia mesenteric", "Acute mesenteric ischemia", "Acute intestinal ischaemia", "acute intestinal ischaemia", "acute mesenteric ischaemia", "Acute mesenteric ischaemia", "acute GIT vascular insuffic.", "AMI - Acute mesenteric ischemia", "AMI - Acute mesenteric ischaemia", "Acute intestinal ischemic syndrome", "Acute intestinal ischaemic syndrome", "acute intestinal vascular insufficiency", "Acute intestinal vascular insufficiency", "Acute intestinal ischemic syndrome, NOS", "MESENTERIC VASCULAR INSUFFICIENCY, ACUTE", "Acute intestinal ischaemic syndrome, NOS", "acute vascular insufficiency of intestine", "Acute vascular insufficiency of intestine", "Acute vascular insufficiency of intestine, NOS", "acute gastrointestinal tract vascular insuffic.", "Acute vascular insufficiency of intestine (disorder)", "acute vascular insufficiency of intestine (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute intestinal ischemia", "shortest_name_length": 22}
{"curie": "MONDO:0060457", "names": ["AIADK", "AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS", "AUTOINFLAMMATION with arthritis and dyskeratosis", "autoinflammation with arthritis and dyskeratosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoinflammation with arthritis and dyskeratosis", "shortest_name_length": 5}
{"curie": "MONDO:0019420", "names": ["X-linked intellectual disability Pai type", "X-linked intellectual disability, Pai type", "X-linked intellectual disability Pai type (disorder)", "X-linked intellectual disability Pai type (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability, Pai type", "shortest_name_length": 41}
{"curie": "MONDO:0015649", "names": ["micturation-induced seizures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "micturation-induced seizures", "shortest_name_length": 28}
{"curie": "MONDO:0018060", "names": ["congenital fibrinogen deficiency", "fibrinogen deficiency, congenital"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital fibrinogen deficiency", "shortest_name_length": 32}
{"curie": "UMLS:C0920192", "names": ["Descemetitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Descemetitis", "shortest_name_length": 12}
{"curie": "UMLS:C0751068", "names": ["Acquired Deafness", "Deafness, Acquired"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Deafness, Acquired", "shortest_name_length": 17}
{"curie": "UMLS:C1335097", "names": ["Occult Lung Cancer", "Occult Lung Carcinoma", "Occult Carcinoma of Lung", "Occult Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Occult Lung Carcinoma", "shortest_name_length": 18}
{"curie": "MONDO:0021272", "names": ["inherited orthostatic hypotension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited orthostatic hypotension", "shortest_name_length": 33}
{"curie": "UMLS:C5206810", "names": ["Locally Advanced Gastric Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Gastric Adenocarcinoma", "shortest_name_length": 39}
{"curie": "UMLS:C4687513", "names": ["Locally Advanced Epithelioid Hemangioendothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Epithelioid Hemangioendothelioma", "shortest_name_length": 49}
{"curie": "UMLS:C5204273", "names": ["Renal Paraganglioma", "Kidney Paraganglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kidney Paraganglioma", "shortest_name_length": 19}
{"curie": "UMLS:C0852910", "names": ["birth mark", "Birth mark", "birth marks", "Birth mark NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Birth mark", "shortest_name_length": 10}
{"curie": "UMLS:C1333832", "names": ["Grade 1 Invasive Breast Carcinoma", "Grade 1 Infiltrating Breast Carcinoma", "Favorable Infiltrating Breast Carcinoma", "Well Differentiated Invasive Breast Carcinoma", "Well Differentiated Infiltrating Breast Carcinoma", "Low Combined Histologic Grade Infiltrating Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade 1 Invasive Breast Carcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C4054395", "names": ["Nephrotic Syndrome - CFH Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - CFH Associated", "shortest_name_length": 35}
{"curie": "MONDO:0013654", "names": ["ANIB11", "intracranial berry aneurysm 11", "aneurysm, intracranial BERRY, 11", "ANEURYSM, INTRACRANIAL BERRY, 11", "aneurysm, intracranial berry, 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aneurysm, intracranial berry, 11", "shortest_name_length": 6}
{"curie": "UMLS:C1442906", "names": ["Talc granuloma", "Talc Granuloma", "talc; granuloma", "granuloma; talc"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Talc granuloma", "shortest_name_length": 14}
{"curie": "MONDO:0031006", "names": ["NDAXOA", "neurodegeneration with ataxia and late-onset optic atrophy", "NEURODEGENERATION WITH ATAXIA AND LATE-ONSET OPTIC ATROPHY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodegeneration with ataxia and late-onset optic atrophy", "shortest_name_length": 6}
{"curie": "MONDO:0009823", "names": ["HP1", "PH1", "Oxalosis I", "OXALOSIS I", "oxalosis I", "Oxalosis 1", "Oxalosis type I", "glycolic aciduria", "GLYCOLIC ACIDURIA", "Glycolic aciduria", "type I hyperoxaluria", "HEPATIC AGT DEFICIENCY", "Hepatic AGT Deficiency", "hepatic AGT deficiency", "AGXT primary hyperoxaluria", "Primary hyperoxaluria type 1", "primary hyperoxaluria type i", "Primary hyperoxaluria type I", "Primary Hyperoxaluria Type I", "primary hyperoxaluria type 1", "primary hyperoxaluria type I", "Primary hyperoxaluria, type I", "glycolic aciduria (diagnosis)", "hyperoxaluria, primary, type I", "hyperoxaluria, primary, type 1", "Hyperoxaluria, Primary, Type I", "HYPEROXALURIA, PRIMARY, TYPE I", "type I hyperoxaluria (diagnosis)", "Primary hyperoxaluria, type I (disorder)", "serine:pyruvate aminotransferase deficiency", "SERINE:PYRUVATE AMINOTRANSFERASE DEFICIENCY", "Serine:Pyruvate Aminotransferase Deficiency", "serine pyruvate aminotransferase deficiency", "alanine-glyoxylate aminotransferase deficiency", "Alanine-glyoxylate aminotransferase deficiency", "ALANINE-GLYOXYLATE AMINOTRANSFERASE DEFICIENCY", "Alanine-glycoxylate aminotransferase deficiency", "2-Oxoglutarate glyoxylate carboligase deficiency", "primary hyperoxaluria caused by mutation in AGXT", "peroxisomal alanine-glyoxylate aminotransferase deficiency", "peroxisomal alanine:glyoxylate aminotransferase deficiency", "Peroxisomal Alanine:Glyoxylate Aminotransferase Deficiency", "Peroxisomal alanine-glyoxylate aminotransferase deficiency", "peroxisomal alanine glyoxylate aminotransferase deficiency", "PEROXISOMAL ALANINE:GLYOXYLATE AMINOTRANSFERASE DEFICIENCY", "Peroxisomal alanine glyoxylate aminotransferase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary hyperoxaluria type 1", "shortest_name_length": 3}
{"curie": "MONDO:0022972", "names": ["diabetic mastopathy", "Diabetic mastopathy", "lymphocytic mastitis", "Lymphocytic mastitis", "lymphocytic mastopathy", "diabetic fibrous mastopathy", "diabetes mellitus mastopathy", "Diabetic mastopathy (diagnosis)", "diabetic fibrous breast disease", "sclerosing lymphocytic lobulitis", "Sclerosing lymphocytic lobulitis", "Mastopathy due to diabetes mellitus", "Sclerosing lymphocytic lobulitis of the breast", "Mastopathy due to diabetes mellitus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diabetic mastopathy", "shortest_name_length": 19}
{"curie": "MONDO:0020064", "names": ["PVA", "Absent pulmonary valve", "Pulmonary valve agenesis", "pulmonary valve agenesis", "pulmonary valves agenesis", "Absence of the pulmonary valve", "Absent pulmonary valve syndrome", "absent pulmonary valve syndrome", "Congenital absence of pulmonic valve", "Congenital absence of pulmonary valve", "congenital absence of pulmonary valve", "Congenital absence of the pulmonary valve", "congenital absence of the pulmonary valve", "pulmonary valve congenital malformation absence", "Congenital absence of pulmonary valve (disorder)", "congenital absence of pulmonary valve (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary valve agenesis", "shortest_name_length": 3}
{"curie": "MONDO:0011165", "names": ["GFND2", "fibronectin glomerulopathy", "FN1 fibronectin glomerulopathy", "Glomerulopathy with Fibronectin Deposits-2", "Glomerulopathy with fibronectin deposits 2", "glomerulopathy with fibronectin deposits 2", "GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2", "Glomerulopathy With Fibronectin Deposits 2", "glomerulopathy with fibronectin deposits type 2", "fibronectin glomerulopathy caused by mutation in FN1", "Glomerulopathy with fibronectin deposits 2 (disorder)", "GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 (disorder)", "glomerulopathy with fibronectin deposits 2 (diagnosis)", "glomerular nephritis familial with fibronectin deposits", "glomerular nephritis, familial, with fibronectin deposits"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glomerulopathy with fibronectin deposits 2", "shortest_name_length": 5}
{"curie": "UMLS:C4527240", "names": ["pLCIS", "PLCIS", "Breast Pleomorphic Lobular Carcinoma In Situ", "Pleomorphic Lobular Breast Carcinoma In Situ", "Pleomorphic lobular carcinoma in situ of breast", "Pleomorphic Lobular Carcinoma in Situ of the Breast", "Non-Invasive Pleomorphic Lobular Carcinoma of the Breast", "Pleomorphic lobular carcinoma in situ of breast (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pleomorphic lobular carcinoma in situ of breast", "shortest_name_length": 5}
{"curie": "UMLS:C5230993", "names": ["Cutaneous epithelioid angiomatoid nodule", "Cutaneous epithelioid angiomatous nodule", "Cutaneous Epithelioid Angiomatous Nodule", "Cutaneous epithelioid angiomatoid nodule (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous epithelioid angiomatoid nodule", "shortest_name_length": 40}
{"curie": "UMLS:C3160944", "names": ["Vulvovaginal swelling"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvovaginal swelling", "shortest_name_length": 21}
{"curie": "MONDO:0003557", "names": ["Optic nerve sheath meningioma", "optic nerve sheath meningioma", "Optic Nerve Sheath Meningioma", "meningiomas nerve optic sheath", "Meningioma of optic nerve sheath", "Meningioma of Optic Nerve Sheath", "meningioma of optic nerve sheath", "Meningioma of the Optic Nerve Sheath", "meningioma of the optic nerve sheath", "Meningioma of optic nerve sheath (disorder)", "Meningioma of optic nerve sheath (diagnosis)", "meningeal neoplasm optic nerve sheath meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "optic nerve sheath meningioma", "shortest_name_length": 29}
{"curie": "MONDO:0002810", "names": ["Pancreatic Serous Neoplasm", "pancreatic serous neoplasm", "Pancreatic Serous Cystic Neoplasm", "pancreatic serous cystic neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic serous cystic neoplasm", "shortest_name_length": 26}
{"curie": "MONDO:0024771", "names": ["MPD7", "MYOPATHY, DISTAL, 7, ADULT-ONSET, X-LINKED", "myopathy, distal, 7, adult-onset, X-linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy, distal, 7, adult-onset, X-linked", "shortest_name_length": 4}
{"curie": "UMLS:C0542351", "names": ["BATTERY", "Battery", "battery", "Battery (event)", "assault battery", "battery [assault]", "Battery (assault)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Battery (assault)", "shortest_name_length": 7}
{"curie": "MONDO:0015325", "names": ["Schaap-Taylor-Baraitser syndrome", "Schaap Taylor Baraitser syndrome", "cataract-deafness-hypogonadism syndrome", "Cataract-deafness-hypogonadism syndrome", "Cataract-hearing loss-hypogonadism syndrome", "Congenital cataract with deafness and hypogonadism syndrome", "congenital cataract with deafness and hypogonadism syndrome", "Congenital cataract with deafness and hypogonadism syndrome (disorder)", "congenital cataract with deafness and hypogonadism syndrome (diagnosis)", "Cataracts, sensorineural deafness, hypogonadism, hypertrichosis and short stature", "cataracts, sensorineural deafness, hypogonadism, hypertrichosis and short stature"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract-deafness-hypogonadism syndrome", "shortest_name_length": 32}
{"curie": "UMLS:C1265736", "names": ["OOC", "Orthokeratinised odontogenic cyst", "Orthokeratinized Odontogenic Cyst", "Orthokeratinized odontogenic cyst", "Orthokeratinized odontogenic cyst (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Orthokeratinized odontogenic cyst", "shortest_name_length": 3}
{"curie": "UMLS:C3828621", "names": ["Pediatric Non-congenital Ventricular Tachycardia", "Pediatric Non-Congenital Ventricular Tachycardia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pediatric Non-Congenital Ventricular Tachycardia", "shortest_name_length": 48}
{"curie": "UMLS:C0886477", "names": ["Malignant Testicular Germ Cell Tumor", "Childhood Malignant Testicular Germ Cell Tumor", "childhood malignant testicular germ cell tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Malignant Testicular Germ Cell Tumor", "shortest_name_length": 36}
{"curie": "UMLS:C3899676", "names": ["Anaplastic Oligoastrocytoma", "childhood anaplastic oligoastrocytoma", "Childhood Anaplastic Oligoastrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Anaplastic Oligoastrocytoma", "shortest_name_length": 27}
{"curie": "UMLS:C5205915", "names": ["Metastatic Clear Cell Sarcoma of Soft Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Clear Cell Sarcoma of Soft Tissue", "shortest_name_length": 44}
{"curie": "MONDO:0015091", "names": ["SPG9", "spastic paraplegia 9", "autosomal dominant spastic paraparesis", "autosomal dominant spastic paraplegia type 9", "ALDH18A1 autosomal dominant complex spastic paraplegia", "cataracts-motor neuropathy-short stature-skeletal anomalies syndrome", "cataracts, motor neuronopathy, short stature and skeletal abnormalities", "spastic paraparesis-amyopathy-cataracts-gastroesophageal reflux syndrome", "autosomal dominant complex spastic paraplegia caused by mutation in ALDH18A1", "bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant spastic paraplegia type 9", "shortest_name_length": 4}
{"curie": "UMLS:C5670678", "names": ["Stage IIA2 Cervical Cancer FIGO 2009", "Stage IIA2 Cervical Carcinoma FIGO 2009"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA2 Cervical Cancer FIGO 2009", "shortest_name_length": 36}
{"curie": "UMLS:C4521609", "names": ["Stage II Pleural Malignant Mesothelioma", "Stage II Pleural Malignant Mesothelioma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Pleural Malignant Mesothelioma AJCC v8", "shortest_name_length": 39}
{"curie": "MONDO:0010731", "names": ["SDYS", "DGSX", "Sgbs", "SGBS", "SGBS1", "SGB syndrome", "Bulldog syndrome", "simpson syndrome", "Sara Angers syndrome", "Golabi-Rosen syndrome", "Simpson dysplasia syndrome", "Simpson dysmorphia syndrome", "Golabi-Rosen syndrome (GRS)", "Simpson Dysmorphia Syndrome", "simpson dysmorphia syndrome", "simpson-golabi-behmel syndrome", "simpson golabi behmel syndrome", "Simpson-Golabi-Behmel syndrome", "Simpson-Golabi-Behmel Syndrome", "Simpson dysmorphia syndrome (SDYS)", "X-linked dysplasia gigantism syndrome", "X-linked dysplasia-gigantism syndrome", "Simpson-Golabi-Behmel syndrome type 1", "mental retardation-overgrowth syndrome", "dysplasia gigantism syndrome, X-linked", "Simpson-Golabi-Behmel syndrome (disorder)", "Simpson-Golabi-Behmel (SGB) syndrome (SGBS)", "X-linked dysplasia-gigantism syndrome (DGSX)", "bulldog syndrome dysplasia-gigantism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Simpson-Golabi-Behmel syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0018810", "names": ["lethal hydranencephaly-diaphragmatic hernia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal hydranencephaly-diaphragmatic hernia syndrome", "shortest_name_length": 52}
{"curie": "MONDO:0014175", "names": ["MTDPS12", "MTDPS12B", "mitochondrial DNA depletion syndrome 12", "Mitochondrial DNA Depletion Syndrome 12", "mitochondrial DNA depletion syndrome 12b", "mitochondrial DNA depletion syndrome type 12", "mitochondrial DNA depletion syndrome 12 (cardiomyopathic type)", "mitochondrial DNA depletion syndrome 12B (cardiomyopathic type) AR", "mitochondrial DNA depletion syndrome 12B (cardiomyopathic type), AR", "mitochondrial DNA depletion syndrome 12B (cardiomyopathic type), autosomal recessive", "MITOCHONDRIAL DNA DEPLETION SYNDROME 12B (CARDIOMYOPATHIC TYPE), AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial DNA depletion syndrome 12B (cardiomyopathic type), autosomal recessive", "shortest_name_length": 7}
{"curie": "MONDO:0032922", "names": ["BEFAHRS", "Beck-Fahrner syndrome", "BECK-FAHRNER SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Beck-Fahrner syndrome", "shortest_name_length": 7}
{"curie": "UMLS:C0022099", "names": ["Irradiated bone marrow", "Bone Marrow Radiation Injury", "Hematopoietic Radiation Injury", "HEMATOPOIETIC RADIATION INJURY", "Radiation injury of bone marrow", "Radiation injury of bone marrow (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radiation injury of bone marrow", "shortest_name_length": 22}
{"curie": "UMLS:C0025319", "names": ["MENOPAUSE SYNDROME", "syndrome menopause", "menopause syndrome", "menopausal syndrome", "Syndrome menopausal", "MENOPAUSAL DISORDER", "Menopausal disorder", "menopausal disorder", "Menopausal Syndrome", "MENOPAUSAL SYNDROME", "Menopausal syndrome", "SYNDROME MENOPAUSAL", "syndrome; menopausal", "menopausal; syndrome", "Menopausal disorders", "menopausal disorders", "disorder; menopausal", "Climacteric syndrome", "climacteric syndrome", "menopausal; disorder", "syndrome; climacteric", "Menopausal syndrome (disorder)", "menopausal disorder (diagnosis)", "Menopausal Syndrome (Hot Flushes)", "disease (or disorder); menopausal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Menopausal syndrome", "shortest_name_length": 18}
{"curie": "MONDO:0011944", "names": ["SLEN3", "systemic lupus erythematosus with nephritis, susceptibility to, 3", "SYSTEMIC LUPUS ERYTHEMATOSUS WITH NEPHRITIS, SUSCEPTIBILITY TO, 3", "SYSTEMIC LUPUS ERYTHEMATOSUS WITH NEPHRITIS, SUSCEPTIBILITY TO, 3 (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "systemic lupus erythematosus with nephritis, susceptibility to, 3", "shortest_name_length": 5}
{"curie": "MONDO:0037746", "names": ["Malignant Vaginal Mixed Epithelial and Mesenchymal Tumor", "malignant vaginal mixed epithelial and mesenchymal tumor", "Malignant Vaginal Mixed Epithelial and Mesenchymal Neoplasm", "malignant vaginal mixed epithelial and mesenchymal neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant vaginal mixed epithelial and mesenchymal neoplasm", "shortest_name_length": 56}
{"curie": "MONDO:0006047", "names": ["PAAD", "Pancreas Adenocarcinoma", "Adenocarcinoma pancreas", "adenocarcinoma pancreas", "pancreas adenocarcinoma", "adenocarcinoma - pancreas", "Pancreatic Adenocarcinoma", "Pancreatic adenocarcinoma", "Adenocarcinoma - pancreas", "pancreatic adenocarcinoma", "Adenocarcinoma of Pancreas", "adenocarcinoma of pancreas", "Adenocarcinoma of pancreas", "adenocarcinoma of the pancreas", "Adenocarcinoma of the Pancreas", "Adenocarcinoma of the pancreas", "Adenocarcinoma of pancreas (disorder)", "adenocarcinoma of pancreas (diagnosis)", "pancreatic neoplasm malignant adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic adenocarcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0013801", "names": ["DEE13", "EIEE13", "SCN8A epilepsy", "SCN8A encephalopathy", "Encephalopathy, Early Infantile, 13", "SCN8A-related epilepsy with encephalopathy", "epilepsy SCN8A-related with encephalopathy", "Early infantile epileptic encephalopathy 13", "early infantile epileptic encephalopathy-13", "early infantile epileptic encephalopathy 13", "epileptic encephalopathy, early infantile, 13", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 13", "Developmental and Epileptic Encephalopathy 13", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 13", "developmental and epileptic encephalopathy 13", "SCN8A early infantile epileptic encephalopathy", "developmental and epileptic encephalopathy, 13", "epileptic encephalopathy, early infantile, type 13", "early infantile epileptic encephalopathy caused by mutation in SCN8A", "Sodium voltage-gated channel alpha subunit 8-related epilepsy with encephalopathy", "SCN8A (sodium voltage-gated channel alpha subunit 8) related epilepsy with encephalopathy", "Sodium voltage-gated channel alpha subunit 8-related epilepsy with encephalopathy (disorder)", "Sodium voltage-gated channel alpha subunit 8-related epilepsy with encephalopathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 13", "shortest_name_length": 5}
{"curie": "MONDO:0002640", "names": ["nerve optic tumor", "tumor optic nerve", "optic nerve tumor", "Optic Nerve Tumor", "optic nerve tumour", "nerve optic tumors", "Optic nerve--Tumors", "tumor of optic nerve", "optic nerve neoplasm", "Optic nerve neoplasm", "Tumor of Optic Nerve", "Optic Nerve Neoplasm", "Tumor of optic nerve", "Optic Nerve Neoplasms", "Neoplasm, Optic Nerve", "optic nerve neoplasms", "Tumour of optic nerve", "tumour of optic nerve", "cranial nerve II tumor", "Neoplasms, Optic Nerve", "neoplasms, optic nerve", "Neoplasm of optic nerve", "neoplasm of optic nerve", "Neoplasm of Optic Nerve", "Tumor of the Optic Nerve", "tumor of the optic nerve", "cranial nerve II neoplasm", "tumor of cranial nerve II", "Cranial Nerve II Neoplasms", "Second Cranial Nerve Tumor", "cranial nerve II neoplasms", "second cranial nerve tumor", "neoplasm of the optic nerve", "Neoplasm of the Optic Nerve", "neoplasm of optic nerve (II)", "neoplasm of cranial nerve II", "Tumor of Second Cranial Nerve", "Second Cranial Nerve Neoplasm", "tumor of Second Cranial nerve", "tumor of second cranial nerve", "second cranial nerve neoplasm", "Second Cranial Nerve Neoplasms", "second cranial nerve neoplasms", "neoplasms, second cranial nerve", "Neoplasms, Second Cranial Nerve", "Neoplasm of Second Cranial Nerve", "neoplasm of second cranial nerve", "Tumor of the Second Cranial Nerve", "tumor of the second cranial nerve", "Neoplasm of optic nerve (disorder)", "cranial nerve II neoplasm (disease)", "Neoplasm of the Second Cranial Nerve", "neoplasm of the second cranial nerve", "neoplasm of optic nerve (II) (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "optic nerve neoplasm", "shortest_name_length": 17}
{"curie": "UMLS:C0037140", "names": ["Simian B disease", "B virus infection", "B Virus Infection", "Infection, B Virus", "B Virus Infections", "Infections, B Virus", "Herpesvirus B infection", "Herpes simiae infection", "Simian B disease (disorder)", "Cercopithecine herpesvirus 1 disease", "disease (or disorder); simian B (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B Virus Infection", "shortest_name_length": 16}
{"curie": "MONDO:0010930", "names": ["Anophthalmia-Plus Syndrome", "anophthalmia-plus syndrome", "anophthalmia plus syndrome", "Anophthalmia plus syndrome", "ANOPHTHALMIA-PLUS SYNDROME", "Fryns anophthalmia syndrome", "Leichtman Wood Rohn syndrome", "Fryns Microphthalmia Syndrome", "FRYNS MICROPHTHALMIA SYNDROME", "Fryns microphthalmia syndrome", "Microphthalmia with facial clefting", "microphthalmia with facial clefting", "MICROPHTHALMIA WITH FACIAL CLEFTING", "Microphthalmia with Facial Clefting", "Anophthalmia plus syndrome (disorder)", "anophthalmia, cleft lip/palate, facial anomalies, and CNS anomalies and hypothalamic disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anophthalmia plus syndrome", "shortest_name_length": 26}
{"curie": "MONDO:0018594", "names": ["Scondary PAN", "secondary PAN", "secondary periarteritis nodosa", "secondary polyarteritis nodosa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary polyarteritis nodosa", "shortest_name_length": 12}
{"curie": "MONDO:0024379", "names": ["ISWD", "irregular sleep-wake rhythm", "Irregular sleep-wake pattern", "irregular sleep-wake pattern", "irregular sleep-wake disorder", "irregular sleep-wake rhythm (diagnosis)", "Irregular sleep-wake pattern (disorder)", "circadian rhythm sleep disorder, irregular sleep wake type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "circadian rhythm sleep disorder, irregular sleep wake type", "shortest_name_length": 4}
{"curie": "MONDO:0001646", "names": ["Secondary benign hypertension", "benign secondary hypertension", "Benign secondary hypertension", "Benign Secondary Hypertension", "secondary hypertension benign", "Secondary hypertension, benign", "Secondary benign hypertension (disorder)", "benign secondary hypertension (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign secondary hypertension", "shortest_name_length": 29}
{"curie": "MONDO:0013432", "names": ["MGORS5", "Meier-Gorlin syndrome 5", "Meier-GORLIN syndrome 5", "MEIER-GORLIN SYNDROME 5", "CDC6 Meier-Gorlin syndrome", "Meier-Gorlin syndrome type 5", "Meier-Gorlin syndrome caused by mutation in CDC6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meier-Gorlin syndrome 5", "shortest_name_length": 6}
{"curie": "MONDO:0016700", "names": ["ependymal tumors", "Ependymal neoplasm", "Malignant ependymoma", "Malignant Ependymoma", "Ependymoma malignant", "malignant ependymoma", "high grade ependymoma", "Anaplastic ependymoma", "anaplastic ependymoma", "high-grade ependymoma", "ependymoma, malignant", "Anaplastic Ependymoma", "Anaplastic Ependymomas", "Ependymoma, anaplastic", "Ependymoma, Anaplastic", "Ependymomas, Anaplastic", "Anaplastic Ependymal Tumor", "anaplastic ependymal tumor", "WHO Grade 3 Ependymal Tumor", "undifferentiated ependymoma", "Ependymoma, anaplastic type", "Undifferentiated Ependymoma", "anaplastic ependymal neoplasm", "WHO Grade III Ependymal Tumor", "WHO grade III ependymal tumor", "Anaplastic Ependymal Neoplasm", "WHO Grade 3 Ependymal Neoplasm", "Malignant epithelial ependymoma", "WHO Grade III Ependymal Neoplasm", "WHO grade III ependymal neoplasm", "Undifferentiated Ependymal Tumor", "undifferentiated ependymal tumor", "malignant ependymoma (diagnosis)", "CNS neoplasm malignant ependymoma", "ependymoma, anaplastic, malignant", "undifferentiated ependymal neoplasm", "Undifferentiated Ependymal Neoplasm", "Malignant ependymoma (morphologic abnormality)", "Ependymoma, anaplastic (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anaplastic ependymoma", "shortest_name_length": 16}
{"curie": "MONDO:0010371", "names": ["AIED", "Aland disease", "Aland island eye disease", "Aland Island eye disease", "ALAND ISLAND eye disease", "Ocular albinism, type II", "ALAND ISLAND EYE DISEASE", "Aland Island Eye Disease", "Åland Islands eye disease", "Forsius-Eriksson syndrome", "Forsius Eriksson type ocular albinism", "Forsius-Eriksson Type Ocular Albinism", "FORSIUS-ERIKSSON TYPE OCULAR ALBINISM", "FORSIUS-Eriksson type ocular albinism", "Forsius-Eriksson type ocular albinism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aland island eye disease", "shortest_name_length": 4}
{"curie": "UMLS:C2981376", "names": ["Stage IIIB Esophageal Squamous Cell Cancer", "Stage IIIB Esophageal Squamous Cell Carcinoma", "Stage IIIB Esophageal Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Esophageal Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 42}
{"curie": "MONDO:0005922", "names": ["tb pleura", "tb pleurisy", "TB of pleura", "pleurisy, tb", "Pearly disease", "pearly disease", "pleura; tuberculous", "pleura tuberculosis", "pleural tuberculosis", "Pleural Tuberculosis", "PLEURAL TUBERCULOSIS", "Pleurisy;tuberculous", "Pleural Tuberculoses", "tuberculosis; pleura", "Tuberculous pleurisy", "TUBERCULOUS PLEURISY", "tuberculous pleurisy", "Pleura--Tuberculosis", "tuberculosis pleural", "Tuberculous Pleurisy", "tuberculosis pleurisy", "Tuberculous Pleuritis", "Pleurisy, Tuberculous", "Tuberculoses, Pleural", "pleurisy; tuberculous", "Tuberculous pleuritis", "Tuberculosis, Pleural", "tuberculous pleuritis", "tuberculosis; pleurisy", "tuberculosis of pleura", "Tuberculosis of pleura", "Tuberculosis of Pleura", "Tuberculous Pleurisies", "Pleurisies, Tuberculous", "Tuberculosis of pleura (disorder)", "tuberculosis pleurisy (diagnosis)", "Tuberculous pleurisy, unspecified", "TB pleurisy in primary progressive TB", "Tuberculous pleurisy in primary progressive tuberculosis", "tuberculous pleurisy in primary progressive tuberculosis", "Primary progressive tuberculosis with tuberculous pleurisy", "Tuberculous pleurisy in primary progressive tuberculosis (disorder)", "tuberculous pleurisy in primary progressive tuberculosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pleural tuberculosis", "shortest_name_length": 9}
{"curie": "MONDO:0018343", "names": ["periodic paralysis with later-onset distal motor neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "periodic paralysis with later-onset distal motor neuropathy", "shortest_name_length": 59}
{"curie": "UMLS:C5421312", "names": ["Retroperitoneal Undifferentiated Pleomorphic Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retroperitoneal Undifferentiated Pleomorphic Sarcoma", "shortest_name_length": 52}
{"curie": "UMLS:C0854810", "names": ["Recurrent Lymphocyte Depleted Hodgkin Lymphoma", "Recurrent Lymphocyte Depleted Hodgkin's Lymphoma", "Recurrent Hodgkin's Lymphoma Lymphocyte Depleted", "Relapsed Hodgkin's Disease Lymphocyte Depletion Type", "Hodgkin's disease lymphocyte depletion type recurrent", "Relapsed Hodgkin's Lymphoma Lymphocyte Depletion Type", "Recurrent Hodgkin's Disease Lymphocyte Depletion Type", "Recurrent Hodgkin's Lymphoma Lymphocyte Depletion Type", "Recurrent Lymphocyte-Depleted Classic Hodgkin Lymphoma", "Recurrent Lymphocyte-Depleted Classical Hodgkin Lymphoma", "Recurrent Lymphocyte Depleted Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's disease lymphocyte depletion type recurrent", "shortest_name_length": 46}
{"curie": "MONDO:0020650", "names": ["germ cell tumor of the vulva"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "germ cell tumor of the vulva", "shortest_name_length": 28}
{"curie": "MONDO:0013429", "names": ["RP40", "retinitis pigmentosa 40", "RETINITIS PIGMENTOSA 40", "retinitis pigmentosa-40", "PDE6B retinitis pigmentosa", "retinitis pigmentosa type 40", "RETINITIS PIGMENTOSA 40 (disorder)", "retinitis pigmentosa caused by mutation in PDE6B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 40", "shortest_name_length": 4}
{"curie": "UMLS:C0232910", "names": ["teratosis", "teratogenesis", "Teratogenesis", "Teratogenicity", "teratogenicity", "TERATOGENICITY", "dysmorphogenesis", "effect teratogenic", "Teratogenic Effect", "Teratogenic effect", "teratogenic effect", "effects teratogenic", "abnormal embryogenesis", "Teratogenesis (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Teratogenesis", "shortest_name_length": 9}
{"curie": "UMLS:C0349255", "names": ["Nonorganic Insomnia", "Nonorganic insomnia", "Insomnia, Nonorganic", "Insomnia (non-organic)", "insomnia; nonorganic origin", "nonorganic origin; insomnia", "Nonorganic insomnia (disorder)", "sleep disorder; insomnia type, nonorganic origin", "insomnia type; sleep disorder, nonorganic origin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nonorganic Insomnia", "shortest_name_length": 19}
{"curie": "MONDO:0032623", "names": ["MC1DN18", "nuclear type mitochondrial complex I deficiency 18", "mitochondrial complex 1 deficiency, nuclear type 18", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 18"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 18", "shortest_name_length": 7}
{"curie": "MONDO:0060759", "names": ["NEDAMSS", "IRF2BPL-related regressive neurodevelopmental disorder-dystonia-seizures syndrome", "neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures", "NEURODEVELOPMENTAL DISORDER WITH REGRESSION, ABNORMAL MOVEMENTS, LOSS OF SPEECH, AND SEIZURES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures", "shortest_name_length": 7}
{"curie": "UMLS:C5237308", "names": ["Recurrent Differentiated Thyroid Gland Carcinoma", "Recurrent Follicular/Papillary Thyroid Gland Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Differentiated Thyroid Gland Carcinoma", "shortest_name_length": 48}
{"curie": "MONDO:0006237", "names": ["chloroma", "Chloroma", "chloromas", "myelosarcoma", "Granulocytic Sarcoma", "sarcoma granulocytic", "granulocytic sarcoma", "Granulocytic sarcoma", "Granulocytic Sarcomas", "Sarcoma, Granulocytic", "granulocytic; sarcoma", "sarcoma; granulocytic", "Sarcomas, Granulocytic", "sarcoma, granulocytic, malignant", "granulocytic sarcoma (diagnosis)", "SARCOMA, GRANULOCYTIC, MALIGNANT", "leukemia myeloid sarcoma granulocytic sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "granulocytic sarcoma", "shortest_name_length": 8}
{"curie": "MONDO:0018190", "names": ["SMALED", "spinal muscular atrophy, lower extremity-predominant", "spinal muscular atrophy with lower extremity predominant", "spinal muscular atrophy with lower extremity predominance", "autosomal dominant childhood-onset proximal spinal muscular atrophy", "lower extremity-predominant autosomal dominant proximal spinal muscular atrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant childhood-onset proximal spinal muscular atrophy", "shortest_name_length": 6}
{"curie": "MONDO:0014773", "names": ["MRFACD", "MED13L syndrome", "ASADOLLAHI-RAUCH SYNDROME", "MED13L haploinsufficiency syndrome", "cardiac anomalies - developmental delay - facial dysmorphism syndrome", "mental retardation and distinctive FACIAL features with or without CARDIAC defects", "MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS", "mental retardation and distinctive Facial features with or without Cardiac defects", "intellectual disability and distinctive FACIAL features with or without CARDIAC defects", "intellectual disability and distinctive Facial features with or without Cardiac defects", "intellectual disability and distinctive facial features with or without cardiac defects", "impaired intellectual development and distinctive facial features with or without cardiac defects", "IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiac anomalies - developmental delay - facial dysmorphism syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0003391", "names": ["Vulvar Alveolar Soft Part Sarcoma", "vulvar alveolar soft part sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar alveolar soft part sarcoma", "shortest_name_length": 33}
{"curie": "UMLS:C0160455", "names": ["Retroperitoneum injury with open wound into cavity", "Injury to Retroperitoneum with Open Wound into Cavity", "Injury to retroperitoneum with open wound into cavity", "injury of retroperitoneum with open wound into cavity", "Retroperitoneum injury with open wound into cavity (disorder)", "Injury of retroperitoneum with open wound into abdominal cavity", "injury of retroperitoneum with open wound into cavity (diagnosis)", "Injury to other intra-abdominal organs with open wound into cavity, retroperitoneum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retroperitoneum injury with open wound into cavity", "shortest_name_length": 50}
{"curie": "MONDO:0010727", "names": ["PRTS", "MRXS1", "MRX36", "PARTINGTON SYNDROME", "Partington syndrome", "Partington syndrome (PRTS)", "Partington-Mulley syndrome", "Mental Retardation, X-Linked 36", "MENTAL RETARDATION, X-LINKED 36", "RUSSELL-SILVER SYNDROME, X-LINKED", "Russell-silver syndrome, X-linked", "Russell-Silver Syndrome, X-Linked", "X-linked mental retardation syndrome 1", "Mental retardation, X-linked, syndromic 1", "MENTAL RETARDATION, X-LINKED, SYNDROMIC 1", "X-linked mental retardation syndrome 1 (MRXS1)", "PARTINGTON X-LINKED MENTAL RETARDATION SYNDROME", "Partington X-linked mental retardation syndrome", "Partington x-linked mental retardation syndrome", "RUSSELL-SILVER-LIKE SYNDROME WITH SKIN PIGMENTATION", "Russell-Silver-Like Syndrome with Skin Pigmentation", "Russell-Silver-like syndrome with skin pigmentation", "Partington X-linked intellectual disability syndrome", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 1", "X-linked intellectual deficit-dystonia-dysarthria syndrome", "X-linked intellectual disability-dystonia-dysarthria syndrome", "Mental retardation-dystonic movements-ataxia-seizures syndrome", "mental retardation-dystonic movements-ataxia-seizures syndrome", "X-linked intellectual deficit-dystonia-dysarthria syndrome (disorder)", "X-linked intellectual deficit-dystonia-dysarthria syndrome (diagnosis)", "Mental retardation, X-linked, with dystonic movements, ataxia, and seizures", "MENTAL RETARDATION, X-LINKED, WITH DYSTONIC MOVEMENTS, ATAXIA, AND SEIZURES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Russell-silver syndrome, X-linked", "shortest_name_length": 4}
{"curie": "MONDO:0013279", "names": ["LQT13", "LQT13 (diagnosis)", "long QT syndrome 13", "LONG QT SYNDROME 13", "KCNJ5 long QT syndrome", "long QT syndrome type 13", "long QT syndrome caused by mutation in KCNJ5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "long QT syndrome 13", "shortest_name_length": 5}
{"curie": "MONDO:0009588", "names": ["LMD", "Langer Syndrome", "Langer syndrome", "Langer Mesomelic Dwarfism", "Langer mesomelic dysplasia", "LANGER MESOMELIC DYSPLASIA", "Langer mesomelic dyspalsia", "Langer Mesomelic Dysplasia", "Langer's mesomelic dwarfism", "Homozygous dyschondrosteosis", "Dyschondrosteosis Homozygous", "dyschondrosteosis, homozygous", "DYSCHONDROSTEOSIS, HOMOZYGOUS", "Dyschondrosteosis, homozygous", "Mesomelic dwarfism Langer type", "mesomelic dwarfism, Langer type", "Langer type mesomelic dysplasia", "Langer Type Mesomelic Dysplasia", "Mesomelic dwarfism, Langer type", "Mesomelic dysplasia - Langer type", "Langer type of mesomelic dwarfism", "Langer Mesomelic Dysplasia Syndrome", "Langer mesomelic dysplasia syndrome", "Langer mesomelic dysplasia syndrome (disorder)", "Homozygous Leri-Weill dyschondrosteosis syndrome", "langer mesomelic dysplasia, pseudoautosomal recessive", "mesomelic dwarfism of the hypoplastic ulna, fibula and mandible type", "Mesomelic dwarfism of the hypoplastic ulna, fibula, and mandible type", "mesomelic dwarfism of the hypoplastic ulna, fibula, and mandible type", "MESOMELIC DWARFISM OF THE HYPOPLASTIC ULNA, FIBULA, AND MANDIBLE TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Langer mesomelic dysplasia", "shortest_name_length": 3}
{"curie": "UMLS:C1709831", "names": ["Radiation-Related Non-Neoplastic Disorder", "Radiation-Induced Non-Neoplastic Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radiation-Related Non-Neoplastic Disorder", "shortest_name_length": 41}
{"curie": "MONDO:0013665", "names": ["EJM9", "juvenile myoclonic epilepsy 9", "EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 9", "epilepsy, juvenile myoclonic, susceptibility to, 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, juvenile myoclonic, susceptibility to, 9", "shortest_name_length": 4}
{"curie": "UMLS:C4527251", "names": ["Refractory Anal Cancer", "Refractory Anal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Anal Carcinoma", "shortest_name_length": 22}
{"curie": "MONDO:0000918", "names": ["ENDOMETRITIS", "endometritis", "Endometritis", "Endometritis NOS", "Endometritis, NOS", "Uterine infection", "uterine infection", "Uterine Infection", "Endometritis (disorder)", "endometrium inflammation", "Endometrial inflammation", "endometritis (diagnosis)", "inflammation of endometrium", "Inflammation of the inner lining of the uterus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometritis", "shortest_name_length": 12}
{"curie": "UMLS:C0855040", "names": ["Localized Epithelioid Sarcoma", "Epithelioid Sarcoma, Nonmetastatic", "Epithelioid sarcoma non-metastatic", "Non-Metastatic Epithelioid Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epithelioid sarcoma non-metastatic", "shortest_name_length": 29}
{"curie": "UMLS:C1336167", "names": ["stage IIA non-small cell lung cancer", "Stage IIA Non-Small Cell Lung Cancer", "Stage IIA Non-Oat Cell Lung Carcinoma", "Stage IIA Non-Small Cell Lung Carcinoma", "Stage IIA Non-Oat Cell Carcinoma of Lung", "Stage IIA Non-Small Cell Carcinoma of Lung", "Stage IIA Non-Oat Cell Carcinoma of the Lung", "Stage IIA Non-Small Cell Carcinoma of the Lung", "Stage IIA Non-Small Cell Lung Carcinoma AJCC v7", "Stage IIA Lung Non-Small Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Non-Small Cell Lung Carcinoma AJCC v7", "shortest_name_length": 36}
{"curie": "UMLS:C5205933", "names": ["Prostate Small Lymphocytic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Small Lymphocytic Lymphoma", "shortest_name_length": 35}
{"curie": "MONDO:0011994", "names": ["DFNA41", "autosomal dominant deafness 41", "DEAFNESS, AUTOSOMAL DOMINANT 41", "Deafness, Autosomal Dominant 41", "deafness, autosomal dominant 41", "deafness, autosomal dominant type 41", "DEAFNESS, AUTOSOMAL DOMINANT 41 (disorder)", "autosomal dominant nonsyndromic deafness 41", "P2RX2 autosomal dominant nonsyndromic deafness", "autosomal dominant nonsyndromic hearing loss 41", "autosomal dominant nonsyndromic deafness type 41", "autosomal dominant nonsyndromic deafness caused by mutation in P2RX2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 41", "shortest_name_length": 6}
{"curie": "UMLS:C0271383", "names": ["Symptomatic nystagmus", "nystagmus symptomatic", "Symptomatic Nystagmus", "Nystagmus, symptomatic", "Nystagmus, Symptomatic", "Symptomatic nystagmus (disorder)", "Symptomatic nystagmus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Symptomatic Nystagmus", "shortest_name_length": 21}
{"curie": "MONDO:0014259", "names": ["HMN2D", "DHMN2D", "HMN 2D", "HMN IID", "distal hereditary motor neuropathy type IID", "distal hereditary motor neuronopathy type 2D", "FBXO38 neuronopathy, distal hereditary motor", "neuropathy, distal hereditary motor, type 2D", "NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IID", "neuronopathy, distal hereditary motor, type 2D", "neuronopathy, distal hereditary motor, type IID", "NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IID", "distal spinal muscular atrophy with calf predominance", "neuronopathy, distal hereditary motor caused by mutation in FBXO38", "spinal muscular atrophy, distal, autosomal dominant, calf-predominant", "SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL DOMINANT, CALF-PREDOMINANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuronopathy, distal hereditary motor, type 2D", "shortest_name_length": 5}
{"curie": "UMLS:C1720135", "names": ["Gastrointestinal infection due to Klebsiella mobilis", "Gastrointestinal infection due to Klebsiella aerogenes", "Gastrointestinal infection caused by Klebsiella mobilis", "Gastrointestinal infection caused by Klebsiella aerogenes", "Gastrointestinal infection caused by Aerobacter aerogenes", "Gastrointestinal infection caused by Enterobacter aerogenes", "Gastrointestinal infection due to Klebsiella mobilis (diagnosis)", "Gastrointestinal infection caused by Klebsiella aerogenes (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal infection caused by Klebsiella aerogenes", "shortest_name_length": 52}
{"curie": "MONDO:0032714", "names": ["FHEIG", "FHEIG syndrome", "facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome", "FACIAL DYSMORPHISM, HYPERTRICHOSIS, EPILEPSY, INTELLECTUAL/DEVELOPMENTAL DELAY, AND GINGIVAL OVERGROWTH SYNDROME", "Facial dysmorphism-hypertrichosis-epilepsy-intellectual disability/developmental delay-gingival overgrowth syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0019023", "names": ["CM", "CMCD", "MASTC", "Skin Mastocytoses", "Skin Mastocytosis", "Mastocytosis, Skin", "Mastocytoses, Skin", "MASTOCYTOSIS, INDOLENT", "Cutaneous mastocytosis", "Cutaneous Mastocytoses", "cutaneous mastocytosis", "Cutaneous Mastocytosis", "mastocytosis, cutaneous", "Mastocytosis, Cutaneous", "Mastocytoses, Cutaneous", "MASTOCYTOSIS, CUTANEOUS", "Cutaneous (Skin) Mastocytosis", "cutaneous (skin) mastocytosis", "mastocytosis, systemic, somatic", "cutaneous mastocytosis (disease)", "Cutaneous mastocytosis (disorder)", "cutaneous mastocytosis (diagnosis)", "Cutaneous mastocytosis (morphologic abnormality)", "MASTOCYTOSIS WITH ASSOCIATED HEMATOLOGIC DISORDER"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous mastocytosis", "shortest_name_length": 2}
{"curie": "UMLS:C1336525", "names": ["Submandibular Gland Squamous Cell Carcinoma", "Squamous Cell Carcinoma of Submandibular Gland", "Squamous Cell Carcinoma of the Submandibular Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Submandibular Gland Squamous Cell Carcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0005586", "names": ["head neck tumor", "head neck tumors", "head neck tumours", "head/neck neoplasm", "head neck neoplasms", "Head and neck tumor", "Head and Neck Tumor", "head and neck tumor", "Head and neck tumour", "Head and neck cancer", "Head, Neck Neoplasms", "head or neck neoplasm", "head and neck neoplasm", "tumor of head and neck", "Tumor of head and neck", "Head and Neck Neoplasm", "Tumor of Head and Neck", "Tumour of head and neck", "Head and Neck Neoplasms", "head and neck neoplasia", "head and neck neoplasms", "Neoplasms, Head and Neck", "Neoplasm of Head and Neck", "neoplasm of head and neck", "Neoplasm of head and neck", "Tumor of the Head and Neck", "tumor of the head and neck", "craniocervical region tumor", "Neoplasm of head AND/OR neck", "neoplasm of the head and neck", "Neoplasm of the Head and Neck", "craniocervical region neoplasm", "tumor of craniocervical region", "neoplasm of craniocervical region", "Neoplasm of head AND/OR neck (disorder)", "craniocervical region neoplasm (disease)", "Head and Neck Neoplasm (Excluding Central Nervous System)", "head and neck neoplasm (excluding central nervous system)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "head and neck neoplasm", "shortest_name_length": 15}
{"curie": "MONDO:0015017", "names": ["ASGD8", "anterior segment dysgenesis 8", "ANTERIOR SEGMENT DYSGENESIS 8", "CPAMD8 anterior segment dysgenesis", "anterior segment dysgenesis type 8", "CPAMD8-related anterior segment dysgenesis", "Autosomal recessive anterior segment dysgenesis", "anterior segment dysgenesis caused by mutation in CPAMD8", "Autosomal recessive dysgenesis of anterior segment of eye", "Autosomal recessive dysgenesis of anterior segment of eye (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anterior segment dysgenesis 8", "shortest_name_length": 5}
{"curie": "MONDO:0008678", "names": ["WS", "WMS", "WBS", "Beuren syndrome", "Beuren Syndrome", "William syndrome", "william syndrome", "Monosomy 7q11.23", "deletion 7q11.23", "monosomy 7q11.23", "Deletion 7q11.23", "Syndrome, Beuren", "williams syndrome", "Williams syndrome", "syndrome williams", "WILLIAMS SYNDROME", "Williams Syndrome", "williams' syndrome", "Williams' syndrome", "Syndrome, Williams", "elfin facies syndrome", "syndrome william beuren", "Williams-Beuren Syndrome", "williams-beuren syndrome", "williams beuren syndrome", "Williams Beuren syndrome", "beuren syndrome williams", "WILLIAMS-BEUREN SYNDROME", "Williams-Beuren syndrome", "Williams Beuren Syndrome", "Williams Barratt syndrome", "Williams-Barratt syndrome", "Syndrome, Williams-Beuren", "Williams syndrome (WMS, WS)", "Fanconi-Schlesinger syndrome", "Williams syndrome (disorder)", "Fanconi Schlesinger syndrome", "Williams syndrome (diagnosis)", "Williams-Beuren syndrome (WBS)", "Williams-Beuren Syndrome (WBS)", "Williams Contiguous Gene Syndrome", "Contiguous Gene Syndrome, Williams", "elfin-facies hypercalcemia syndrome", "HYPERCALCEMIA, INFANTILE IDIOPATHIC", "Supravalvar Aortic Stenosis Syndrome", "Chromosome 7q11.23 Deletion Syndrome", "hypercalcemia/Williams-Beuren syndrome", "Hypercalcemia Supravalvar Aortic Stenosis", "Hypercalcemia-Supravalvar Aortic Stenoses", "Hypercalcemia-Supravalvar Aortic Stenosis", "Stenoses, Hypercalcemia-Supravalvar Aortic", "Stenosis, Hypercalcemia-Supravalvar Aortic", "Aortic Stenoses, Hypercalcemia-Supravalvar", "Aortic Stenosis, Hypercalcemia-Supravalvar", "CHROMOSOME 7q11.23 DELETION SYNDROME, 1.5- TO 1.8-MB", "chromosome 7Q11.23 deletion syndrome, 1.5- to 1.8-Mb", "mental retardation-typical facies-aortic stenosis syndrome", "idiopathic hypercalcemia-supravalvular aortic stenosis syndrome", "hypercalcemia-peculiar facies-supravalvular aortic stenosis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Williams syndrome", "shortest_name_length": 2}
{"curie": "UMLS:C5556291", "names": ["Metastatic Microsatellite Stable Ovarian Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Microsatellite Stable Ovarian Carcinoma", "shortest_name_length": 50}
{"curie": "UMLS:C2103575", "names": ["Scleroderma Polymyositis", "polymyositis in scleroderma", "polymyositis in scleroderma (diagnosis)", "Scleroderma Polymyositis Overlap Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polymyositis in scleroderma", "shortest_name_length": 24}
{"curie": "UMLS:C4727064", "names": ["Recurrent Hepatosplenic T-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Hepatosplenic T-Cell Lymphoma", "shortest_name_length": 39}
{"curie": "UMLS:C0362051", "names": ["Primary multicentric tumor", "Primary multicentric tumour", "Malignant Neoplasm of Multiple Primary Sites", "malignant neoplasm of independent multiple sites", "malignancies multiple primary of independent sites", "Primary malignant neoplasm of independent multiple sites", "Malignant neoplasms of independent primary multiple sites", "primary malignant neoplasms of independent multiple sites", "Malignant neoplasms of independent (primary) multiple sites", "malignant neoplasm of independent multiple sites (diagnosis)", "Primary malignant neoplasm of independent multiple sites (disorder)", "primary malignant neoplasms of independent multiple sites (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary malignant neoplasm of independent multiple sites", "shortest_name_length": 26}
{"curie": "MONDO:0056818", "names": ["skin adenosquamous cancer", "Skin Adenosquamous Cancer", "Skin Adenosquamous Carcinoma", "skin adenosquamous carcinoma", "adenosquamous carcinoma of skin", "adenosquamous carcinoma of skin (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin adenosquamous carcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0005031", "names": ["desmoid", "Desmoid", "Desmoids", "desmoids", "fibromatoses", "Desmoid, NOS", "FIBROMATOSIS", "Fibromatosis", "Fibromatoses", "fibromatosis", "Desmoid tumor", "Desmoid Tumor", "desmoid tumor", "desmoid tumour", "Desmoid tumors", "desmoid tumors", "Desmoid tumour", "Desmoid tumours", "desmoid tumours", "Invasive fibroma", "Fibromatosis NOS", "Fibromatosis, NOS", "Deep Fibromatosis", "Deep fibromatosis", "desmoid fibromatosis", "Desmoid Fibromatosis", "fibromatosis desmoid", "Desmoid fibromatosis", "Aggressive fibromatosis", "aggressive fibromatoses", "Aggressive Fibromatosis", "Extra-abdominal desmoid", "aggressive fibromatosis", "Fibromatosis (disorder)", "Aggressive Fibromatoses", "Fibromatoses, Aggressive", "Fibromatosis, Aggressive", "Desmoid type fibromatosis", "Desmoid-Type Fibromatosis", "desmoid tumor (diagnosis)", "Desmoid-type fibromatosis", "Deep fibromatosis (diagnosis)", "Deep Fibromatosis/Desmoid Tumor", "musculoaponeurotic fibromatosis", "Aggressive fibromatosis (disorder)", "Fibromatosis (morphologic abnormality)", "soft tissue neoplasm benign - deep fibromatosis", "Aggressive fibromatosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibromatosis", "shortest_name_length": 7}
{"curie": "UMLS:C1696847", "names": ["Osteomyelitis fungal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Osteomyelitis fungal", "shortest_name_length": 20}
{"curie": "MONDO:0010446", "names": ["bed", "BED", "BORNHOLM EYE DISEASE", "Bornholm eye disease", "Bornholm Eye Disease", "BORNHOLM eye disease", "Bornholm eye disease, X-linked recessive", "X-linked cone dysfunction syndrome with myopia", "MYOPIA, HIGH, WITH NONPROGRESSIVE CONE DYSFUNCTION", "myopia, high, with nonprogressive cone dysfunction", "X-linked cone dysfunction syndrome with myopia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked cone dysfunction syndrome with myopia", "shortest_name_length": 3}
{"curie": "MONDO:0014564", "names": ["CBAS5", "congenital bile acid synthesis defect 5", "bile acid synthesis defect, congenital, 5", "BILE ACID SYNTHESIS DEFECT, CONGENITAL, 5", "ABCD3 congenital bile acid synthesis defect", "congenital bile acid synthesis defect type 5", "bile acid synthesis defect, congenital, type 5", "congenital bile acid synthesis defect caused by mutation in ABCD3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital bile acid synthesis defect 5", "shortest_name_length": 5}
{"curie": "MONDO:0004136", "names": ["ovarian endometrioid cystadenoma", "Ovarian Endometrioid Cystadenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian endometrioid cystadenoma", "shortest_name_length": 32}
{"curie": "MONDO:0010940", "names": ["ASTHMA, BRONCHIAL", "asthma, bronchial", "asthma susceptibility", "Asthma susceptibility", "ASTHMA, SUSCEPTIBILITY TO", "asthma, susceptibility to", "asthma, protection against", "ASTHMA, PROTECTION AGAINST", "asthma susceptibility (diagnosis)", "inherited susceptibility to asthma", "ASTHMA, SUSCEPTIBILITY TO (finding)", "asthma, nocturnal, susceptibility to", "ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO", "asthma-related traits, susceptibility to", "asthma, diminished response to Antileukotriene treatment 1N", "ASTHMA, DIMINISHED RESPONSE TO ANTILEUKOTRIENE TREATMENT IN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited susceptibility to asthma", "shortest_name_length": 17}
{"curie": "MONDO:0008277", "names": ["stomach polyp", "Gastric Polyp", "gastric polyp", "Gastric Polyp(s)", "gastric polyposa", "Gastric Polyposa", "polyps of stomach", "Gastric Polyposis", "Polyps of Stomach", "gastric polyposis", "Polyposis, Gastric", "polyps of the stomach", "Polyps of the Stomach"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stomach polyp", "shortest_name_length": 13}
{"curie": "UMLS:C0581377", "names": ["Decompensated heart failure", "decompensated cardiac failure", "Decompensated cardiac failure", "Decompensated cardiac failure (disorder)", "decompensated cardiac failure (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Decompensated cardiac failure", "shortest_name_length": 27}
{"curie": "OMIM:117800", "names": ["WW", "EWWD", "WET WAX", "EAR WAX, WET/DRY", "CERUMEN, VARIATION IN", "AXILLARY ODOR, VARIATION IN", "COLOSTRUM SECRETION, VARIATION IN", "APOCRINE GLAND SECRETION, VARIATION IN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 2}
{"curie": "MONDO:0035876", "names": ["belinostat toxicity or dose selection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "belinostat toxicity or dose selection", "shortest_name_length": 37}
{"curie": "MONDO:0005420", "names": ["Low T4", "hypothyroid", "Hypothyroid", "HYPOTHYROID", "subthyroidism", "Hypothyreosis", "HYPOTHYROIDISM", "hypothyroidism", "Hypothyroidism", "Hypothyroidisms", "hypothyroidisms", "Thyroid deficiency", "thyroid deficiency", "Hypothyroidism, NOS", "thyroid; deficiency", "Underactive thyroid", "underactive thyroid", "Underactive Thyroid", "deficiency; thyroid", "thyroid insufficiency", "Thyroid insufficiency", "insufficiency; thyroid", "thyroid; insufficiency", "Hypothyroidism (disorder)", "THYROID ACTIVITY DECREASED", "Thyroid activity decreased", "Unspecified hypothyroidism", "hypothyroidism (diagnosis)", "Hypothyroidism, unspecified", "Unspecified acquired hypothyroidism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypothyroidism", "shortest_name_length": 6}
{"curie": "MONDO:0018317", "names": ["growth retardation-mild developmental delay-chronic hepatitis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "growth retardation-mild developmental delay-chronic hepatitis syndrome", "shortest_name_length": 70}
{"curie": "UMLS:C1335524", "names": ["Basal Cell Prostate Hyperplasia", "Prostatic Basal Cell Hyperplasia", "Basal Cell Hyperplasia of Prostate", "Basal Cell Hyperplasia of the Prostate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostatic Basal Cell Hyperplasia", "shortest_name_length": 31}
{"curie": "UMLS:C4526613", "names": ["Stage IVA Thymoma", "Stage IVA Thymoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Thymoma AJCC v8", "shortest_name_length": 17}
{"curie": "MONDO:0005484", "names": ["colorectum adenoma", "Colorectal Adenoma", "colorectal adenoma", "Colorectal adenoma", "Large Bowel Adenoma", "large bowel adenoma", "Colorectal adenomas", "adenoma of large bowel", "Adenoma of Large Bowel", "Large Intestine Adenoma", "large intestine adenoma", "Adenoma of Large Intestine", "Adenoma of large intestine", "Adenoma of the Large Bowel", "adenoma of the large bowel", "adenoma of large intestine", "Adenoma of the Large Intestine", "adenoma of the large intestine", "Adenoma of large intestine (disorder)", "adenoma of large intestine (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorectal adenoma", "shortest_name_length": 18}
{"curie": "UMLS:C0280162", "names": ["Stage III Diffuse Large Cell Lymphoma", "stage III adult diffuse large cell lymphoma", "Adult Diffuse Large Cell Lymphoma Stage III", "Stage III Adult Diffuse Large Cell Lymphoma", "adult diffuse large cell lymphoma, stage III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Adult Diffuse Large Cell Lymphoma", "shortest_name_length": 37}
{"curie": "MONDO:0007037", "names": ["ACH", "ach", "Achondroplasia", "achondroplasia", "ACHONDROPLASIA", "Achondroplasias", "chondrodystrophia", "Chondrodystrophia", "Achondroplastic dwarf", "Achondroplastic Dwarf", "achondroplastic dwarf", "Dwarf, achondroplastic", "Achondroplasia syndrome", "fetal; chondrodysplasia", "Achondroplastic dwarfism", "achondroplastic dwarfism", "Osteosclerosis congenita", "DWARFISM ACHONDROPLASTIC", "Achondroplastic physique", "achondroplastic physique", "osteosclerosis congenita", "achondroplastic; dwarfism", "Chondrodystrophia fetalis", "Congenital osteosclerosis", "Chondrodystrophy syndrome", "Achondroplasia (disorder)", "chondrodysplasia; fetalis", "dwarfism; achondroplastic", "CHONDRODYSTROPHIA FETALIS", "DWARFISM, ACHONDROPLASTIC", "Chondrodystrophia foetalis", "achondroplasia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "achondroplasia", "shortest_name_length": 3}
{"curie": "MONDO:0019105", "names": ["RNS", "nutcracker syndrome", "NCS - nutcracker syndrome", "Renal nutcracker syndrome", "renal nutcracker syndrome", "Renal Nutcracker Syndrome", "Nutcracker Syndrome, Renal", "Renal Nutcracker Syndromes", "Nutcracker Syndromes, Renal", "Renal Vein Entrapment Syndrome", "Left renal vein entrapment syndrome", "left renal vein entrapment syndrome", "Mesoaortic compression of left renal vein", "Left renal vein (LRV) entrapment syndrome", "Left renal vein entrapment syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal nutcracker syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0005810", "names": ["Mono", "Filatow", "Mononucleosis", "MONONUCLEOSIS", "mononucleosis", "Glandular Fever", "Glandular fever", "Kissing disease", "kissing disease", "glandular fever", "kissing; disease", "disease; kissing", "monocytic angina", "Fever, Glandular", "FEVER, GLANDULAR", "Monocytic angina", "Filatov's disease", "monocytic; angina", "angina; monocytic", "pfeiffer's disease", "Pfeiffer's disease", "GF - Glandular fever", "Infective mononucleosis", "Infectious mononucleosis", "INFECTIOUS MONONUCLEOSIS", "Infectious Mononucleosis", "Mononucleosis infectious", "MONONUCLEOSIS INFECTIOUS", "infectious mononucleosis", "Mononucleosis, Infectious", "mononucleosis, infectious", "IM - Infective mononucleosis", "IM - Infectious mononucleosis", "gammaherpesviral mononucleosis", "Gammaherpesviral mononucleosis", "Infectious mononucleosis (disorder)", "infectious mononucleosis (diagnosis)", "Infectious mononucleosis, unspecified", "Epstein-Barr; mononucleosis infectiosa", "mononucleosis, infectious; Epstein-Barr", "Gammaherpesviral mononucleosis (disorder)", "gammaherpesviral; mononucleosis infectiosa", "gammaherpesviral mononucleosis (diagnosis)", "mononucleosis, infectious; gammaherpesviral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infectious mononucleosis", "shortest_name_length": 4}
{"curie": "MONDO:0019671", "names": ["Manus vara", "Radial clubhand", "radial clubhand", "radial hemimelia", "radial ray agenesis", "Manus vara (disorder)", "radial longitidinal meromelia", "congenital longitudinal deficiency of the radius"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radial hemimelia", "shortest_name_length": 10}
{"curie": "MONDO:0004000", "names": ["pilocytic astrocytoma", "Pilocytic Astrocytoma", "childhood pilocytic astrocytoma", "pediatric pilocytic astrocytoma", "Childhood Pilocytic Astrocytoma", "pediatric Pilocytic astrocytoma", "Pediatric Pilocytic Astrocytoma", "pilocytic astrocytoma of childhood", "Pilocytic Astrocytoma of Childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood pilocytic astrocytoma", "shortest_name_length": 21}
{"curie": "UMLS:C3897992", "names": ["Pansclerotic Morphea"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pansclerotic Morphea", "shortest_name_length": 20}
{"curie": "MONDO:0014772", "names": ["OFC15", "OROFACIAL CLEFT 15", "orofacial cleft 15", "DLX4 cleft lip/palate", "orofacial cleft type 15", "cleft lip/palate caused by mutation in DLX4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orofacial cleft 15", "shortest_name_length": 5}
{"curie": "UMLS:C1512906", "names": ["Intestinal Metaplasia of Bladder Urachal Epithelium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal Metaplasia of Bladder Urachal Epithelium", "shortest_name_length": 51}
{"curie": "MONDO:0019773", "names": ["myelocele", "Myelocele", "myeloceles", "Myeloceles", "syringocele", "Syringocele", "Myelocystocele", "Myelomeningocele", "myelomeningocele", "Meningomyelocele", "syringomyelocele", "MENINGOMYELOCELE", "Syringomyelocele", "meningomyelocele", "Meningomyeloceles", "Myelomeningoceles", "meningomyeloceles", "myelomeningoceles", "Myelocele (disorder)", "Spina Bifida Cystica", "Spina bifida cystica", "Hydromeningomyelocele", "Myelocele (diagnosis)", "Hydromyelomeningocele", "Acquired Myelomeningocele", "Acquired Meningomyelocele", "Acquired Meningomyeloceles", "Myelomeningocele, Acquired", "Acquired Myelomeningoceles", "Meningomyelocele, Acquired", "Meningomyelocele (disorder)", "Myelomeningoceles, Acquired", "Meningomyeloceles, Acquired", "meningomyelocele (diagnosis)", "anomaly of spinal cord myelocele"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myelomeningocele", "shortest_name_length": 9}
{"curie": "MONDO:0006531", "names": ["cholesteatoma of attic", "Cholesteatoma of attic", "Cholesteatoma of attic (disorder)", "cholesteatoma of attic (diagnosis)", "Cholesteatoma of attic, unspecified ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholesteatoma of attic", "shortest_name_length": 22}
{"curie": "MONDO:0019206", "names": ["sparse hair-short stature-skin anomalies syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sparse hair-short stature-skin anomalies syndrome", "shortest_name_length": 49}
{"curie": "MONDO:0043797", "names": ["Spinal Cord Injury", "Spinal Cord Trauma", "SPINAL CORD INJURY", "spinal cord trauma", "Injury-spinal cord", "Injury;spinal cord", "spinal cord injury", "Spinal cord injury", "injury, spinal cord", "spinal cord Traumas", "Spinal Cord Traumas", "injury; spinal cord", "Injury, Spinal Cord", "spinal cord; injury", "Cord Injury, Spinal", "Cord Trauma, Spinal", "trauma, spinal cord", "cord injury, spinal", "cord trauma, spinal", "Trauma, Spinal Cord", "Spinal cord syndrome", "traumatic myelopathy", "Cord Traumas, Spinal", "Traumas, spinal cord", "Traumatic Myelopathy", "cord Traumas, spinal", "Spinal Cord Injuries", "spinal cord injuries", "Traumas, Spinal Cord", "cord Injuries, spinal", "Injuries, spinal cord", "Injuries, Spinal Cord", "injury of spinal cord", "spinal cord contusion", "Myelopathy, Traumatic", "myelopathy, traumatic", "Cord Injuries, Spinal", "spinal cord laceration", "traumatic Myelopathies", "spinal cord Contusions", "contusion, spinal cord", "cord contusion, spinal", "Traumatic Myelopathies", "laceration, spinal cord", "Spinal cord injury, NOS", "Myelopathies, traumatic", "cord laceration, spinal", "spinal cord Lacerations", "spinal cord transection", "Myelopathies, Traumatic", "Contusions, spinal cord", "cord Contusions, spinal", "cord transection, spinal", "cord Lacerations, spinal", "SCI - Spinal cord injury", "spinal cord Transections", "transection, spinal cord", "Lacerations, spinal cord", "post traumatic myelopathy", "Transections, spinal cord", "post-traumatic myelopathy", "cord Transections, spinal", "myelopathy, post-traumatic", "post-traumatic Myelopathies", "Myelopathies, post-traumatic", "Spinal cord injury (disorder)", "spinal cord injury (diagnosis)", "Injury of spinal cord, level unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal cord injury", "shortest_name_length": 18}
{"curie": "MONDO:0007509", "names": ["HED", "ECTD10A", "ectodermal dysplasia 10A", "ectodermal dysplasia hypohidrotic autosomal dominant", "hypohidrotic ectodermal dysplasia autosomal dominant", "ECTODERMAL DYSPLASIA, HYPOHIDROTIC, AUTOSOMAL DOMINANT", "ectodermal dysplasia, hypohidrotic, autosomal dominant", "ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT", "ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant", "shortest_name_length": 3}
{"curie": "OMIM:610762", "names": ["HDLCQ6", "High Density Lipoprotein Cholesterol Level QTL6", "HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 6", "High Density Lipoprotein Cholesterol Level Quantitative Trait Locus 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 6}
{"curie": "MONDO:0032611", "names": ["MC1DN6", "nuclear type mitochondrial complex I deficiency 6", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 6", "mitochondrial complex 1 deficiency, nuclear type 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 6", "shortest_name_length": 6}
{"curie": "MONDO:0054845", "names": ["DEE66", "EIEE66", "early infantile epileptic encephalopathy 66", "epileptic encephalopathy, early infantile, 66", "developmental and epileptic encephalopathy 66", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 66", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 66", "developmental and epileptic encephalopathy, 66"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 66", "shortest_name_length": 5}
{"curie": "MONDO:0020745", "names": ["VACRDS", "extrasystoles", "cardiac arrhythmia", "RYR2 CALCIUM RELEASE DEFICIENCY SYNDROME", "autosomal dominant cardiac arrhythmia (Kuhn)", "ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome", "VENTRICULAR ARRHYTHMIAS DUE TO CARDIAC RYANODINE RECEPTOR CALCIUM RELEASE DEFICIENCY SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0005035", "names": ["ganglioneuroblastoma", "Ganglioneuroblastoma", "Ganglioneuroblastomas", "ganglioneuroblastomas", "ganglioneuroblastoma (disease)", "ganglioneuroblastoma, malignant", "Ganglioneuroblastoma (disorder)", "GANGLIONEUROBLASTOMA, MALIGNANT", "ganglioneuroblastoma (diagnosis)", "Ganglioneuroblastoma (morphologic abnormality)", "ganglioneuroblastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ganglioneuroblastoma", "shortest_name_length": 20}
{"curie": "UMLS:C1517577", "names": ["Breast Mixed Carcinoma", "Invasive Breast Mixed Carcinoma", "Invasive Mixed Breast Carcinoma", "Infiltrating Mixed Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Mixed Carcinoma", "shortest_name_length": 22}
{"curie": "UMLS:C5670547", "names": ["Posterior Fossa Ependymoma, NOS", "Posterior Fossa Ependymoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Posterior Fossa Ependymoma, Not Otherwise Specified", "shortest_name_length": 31}
{"curie": "UMLS:C3273048", "names": ["Peripheral ICC", "Peripheral Cholangiocarcinoma", "PERIPHERAL CHOLANGIOCARCINOMA, MALIGNANT", "Small Duct Intrahepatic Cholangiocarcinoma", "Peripheral Intrahepatic Cholangiocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Duct Intrahepatic Cholangiocarcinoma", "shortest_name_length": 14}
{"curie": "MONDO:0010947", "names": ["MOVC", "BDCHS", "Budd-Chiari", "Chiari Syndrome", "syndrome; Chiari", "Chiaris Syndrome", "v.hepatica; block", "Chiari's Syndrome", "block; hepatic vein", "Budd-Chiari Syndrome", "Budd-chiari syndrome", "Syndrome Budd-Chiari", "Budd-Chiari syndrome", "Budd Chiari syndrome", "BUDD CHIARI SYNDROME", "SYNDROME BUDD-CHIARI", "BUDD-CHIARI SYNDROME", "Budd Chiari Syndrome", "Budd-Chiari's syndrome", "LIVER, VEINS, OCCLUSION", "Hepatic vein obstruction", "Chiari; disease or syndrome", "Obstruction of hepatic veins", "Budd-Chiari syndrome, somatic", "Budd-Chiari syndrome (disorder)", "Budd-Chiari syndrome (diagnosis)", "Hepatic venous outflow obstruction", "Hepatic Venous Outflow Obstruction", "Obstruction of hepatic veins syndrome", "Inferior vena cava membranous obstruction", "MEMBRANOUS OBSTRUCTION OF INFERIOR VENA CAVA", "membranous obstruction of Inferior vena cava", "Membranous Obstruction of Inferior Vena Cava", "Membranous obstruction of inferior vena cava", "membranous obstruction of the inferior vena cava", "Membranous obstruction of inferior vena cava (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Budd-Chiari syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0011621", "names": ["ACRPS", "ACRP SYNDROME", "ACRP syndrome", "ACROPECTORAL SYNDROME", "acropectoral syndrome", "Acropectoral syndrome", "acro-pectoral syndrome", "Acro-pectoral syndrome", "DUNDAR ACROPECTORAL SYNDROME", "Dundar Acropectoral syndrome", "Acropectoral syndrome (disorder)", "syndactyly, preaxial polydactyly and sternal deformity", "syndactyly, preaxial polydactyly, and sternal deformity", "SYNDACTYLY, PREAXIAL POLYDACTYLY, AND STERNAL DEFORMITY", "Syndactyly, preaxial polydactyly, and sternal deformity", "Syndactyly-preaxial polydactyly-sternal deformity syndrome", "syndactyly-preaxial polydactyly-sternal deformity syndrome", "Syndactyly with preaxial polydactyly and sternal deformity syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acropectoral syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0002632", "names": ["metachronous osteosarcoma", "Metachronous Osteosarcoma", "metachronous osteosarcoma of the bone", "Metachronous Osteosarcoma of the Bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metachronous osteosarcoma of the bone", "shortest_name_length": 25}
{"curie": "MONDO:0012452", "names": ["DFNB65", "autosomal recessive deafness 65", "Deafness, Autosomal Recessive 65", "DEAFNESS, AUTOSOMAL RECESSIVE 65", "deafness, autosomal recessive 65", "autosomal recessive nonsyndromic deafness 65", "autosomal recessive nonsyndromic hearing loss 65", "autosomal recessive nonsyndromic deafness type 65"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 65", "shortest_name_length": 6}
{"curie": "MONDO:0030493", "names": ["SPGF60", "SPGF 60", "spermatogenic failure 60", "SPERMATOGENIC FAILURE 60"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 60", "shortest_name_length": 6}
{"curie": "UMLS:C1532393", "names": ["Nuchal Fibroma", "Nuchal fibroma", "Nuchal-Type Fibroma", "Nuchal-type fibroma", "Nuchal fibroma (disorder)", "Nuchal-type fibroma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nuchal fibroma", "shortest_name_length": 14}
{"curie": "MONDO:0006552", "names": ["folliculitis", "FOLLICULITIS", "Folliculitis", "Folliculitides", "Folliculitis NOS", "folliculitis nos", "Follicle inflamed", "Follicular pustule", "Hair follicle inflamed", "Folliculitis (disorder)", "hair follicle dermatitis", "folliculitis (diagnosis)", "Hair follicle inflammation", "dermatitis of hair follicle", "Inflammation of hair follicle", "inflammation of hair follicles", "Hair follicle inflammation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "folliculitis", "shortest_name_length": 12}
{"curie": "MONDO:0030908", "names": ["MRXS35", "syndromic X-linked mental retardation 35", "mental retardation, X-linked, syndromic, 35", "MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35", "syndromic X-linked intellectual disability 35", "intellectual disability, X-linked, syndromic, 35", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, 35", "intellectual developmental disorder, X-linked, syndromic, 35, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked, syndromic, 35", "shortest_name_length": 6}
{"curie": "MONDO:0016647", "names": ["autosomal recessive Stickler syndrome", "Stickler syndrome, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive Stickler syndrome", "shortest_name_length": 37}
{"curie": "MONDO:0012139", "names": ["MCDR3", "Mcdr3", "retinal macular dystrophy 3", "macular dystrophy, retinal, 3", "MACULAR DYSTROPHY, RETINAL, 3", "macular dystrophy, retinal, type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macular dystrophy, retinal, 3", "shortest_name_length": 5}
{"curie": "MONDO:0014457", "names": ["HPMRS5", "GPIBD11", "glycosylphosphatidylinositol biosynthesis defect 11", "GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 11", "hyperphosphatasia with mental retardation syndrome 5", "HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 5", "PIGW hyperphosphatasia-intellectual disability syndrome", "hyperphosphatasia with mental retardation syndrome type 5", "hyperphosphatasia with intellectual disability syndrome 5", "hyperphosphatasia with intellectual disability syndrome type 5", "hyperphosphatasia with impaired intellectual development syndrome 5", "hyperphosphatasia-intellectual disability syndrome caused by mutation in PIGW"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperphosphatasia with intellectual disability syndrome 5", "shortest_name_length": 6}
{"curie": "UMLS:C0393672", "names": ["Childhood Benign Psychomotor Epilepsy", "Benign Psychomotor Epilepsy, Childhood", "Epilepsy, Benign Psychomotor, Childhood", "Benign psychomotor epilepsy of childhood", "Benign psychomotor epilepsy of childhood (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epilepsy, Benign Psychomotor, Childhood", "shortest_name_length": 37}
{"curie": "MONDO:0014312", "names": ["ARCND3", "Auriculocondylar syndrome 3", "AURICULOCONDYLAR SYNDROME 3", "AURICULOCONDYLAR syndrome 3", "auriculocondylar syndrome 3", "Auriculocondylar syndrome type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "auriculocondylar syndrome 3", "shortest_name_length": 6}
{"curie": "MONDO:0014784", "names": ["IHPMR", "hypotonia, infantile, with psychomotor retardation", "HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION", "severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0020311", "names": ["cmml", "CMML", "Chronic Myelomonocytic Leukemia", "chronic myelomonocytic leukemia", "Chronic myelomonocytic leukemia", "LEUKEMIA, CHRONIC MYELOMONOCYTIC", "Chronic myelomonocytic leukaemia", "Chronic Myelomonocytic Leukemias", "chronic myelomonocytic leukaemia", "myelomonocytic leukemia, chronic", "Leukemia, Chronic Myelomonocytic", "Myelomonocytic Leukemia, Chronic", "Leukemia, Myelomonocytic, Chronic", "Leukemias, Chronic Myelomonocytic", "myelomonocytic; leukemia, chronic", "Myelomonocytic Leukemias, Chronic", "leukemia; myelomonocytic, chronic", "Chronic myelomonocytic leukemia NOS", "chronic myelomonocytic leukemia (CMML)", "Chronic Myelomonocytic Leukemia (CMML)", "CMML - Chronic myelomonocytic leukemia", "leukemia chronic myelomonocytic (CMML)", "CMML (chronic myelomonocytic leukemia)", "CMML - Chronic myelomonocytic leukaemia", "Chronic myelomonocytic leukemia, Type I", "Chronic myelomonocytic leukaemia, Type I", "Chronic myelomonocytic leukemia, Type II", "Chronic myelomonocytic leukaemia, Type II", "Chronic myelomonocytic leukemia (disorder)", "chronic myelomonocytic leukemia (diagnosis)", "Chronic myelomonocytic leukemia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic myelomonocytic leukemia", "shortest_name_length": 4}
{"curie": "UMLS:C0586323", "names": ["Rumfits", "Rum fits", "alcoholic seizure", "epilepsy; alcohol", "Alcoholic Seizure", "Alcoholic seizure", "Seizure, Alcoholic", "alcoholic seizures", "Alcoholic Seizures", "Seizures, Alcoholic", "Alcohol-related fit", "alcohol related seizure", "Alcohol-Related Seizure", "Seizure, Alcohol-Related", "Alcohol Related Seizures", "Alcohol-Related Seizures", "alcohol related seizures", "Alcohol-induced epilepsy", "Seizures, Alcohol-Related", "Alcohol withdrawal seizure", "alcohol seizure withdrawal", "Alcohol Withdrawal Seizure", "ALCOHOL WITHDRAWAL SEIZURE", "alcohol withdrawal seizure", "alcohol withdrawal seizures", "Seizure, Alcohol Withdrawal", "Alcohol Withdrawal Seizures", "Seizures, Alcohol Withdrawal", "Alcohol-related fit (finding)", "Alcohol withdrawal-induced seizure", "SEIZURE ETIOLOGY ALCOHOL WITHDRAWL", "Alcohol Withdrawal-Induced Seizure", "Alcohol Withdrawal Induced Seizure", "Withdrawal-Induced Seizure, Alcohol", "Alcohol Withdrawal-Induced Seizures", "Alcohol-induced epilepsy (disorder)", "Seizure, Alcohol Withdrawal-Induced", "Seizures, Alcohol Withdrawal-Induced", "Withdrawal-Induced Seizures, Alcohol", "Alcohol withdrawal-induced convulsion", "alcohol withdrawal induced convulsion", "alcohol withdrawal-induced convulsion", "Alcohol withdrawal-induced convulsion (disorder)", "alcohol withdrawal-induced convulsion (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alcohol Withdrawal Seizures", "shortest_name_length": 7}
{"curie": "MONDO:0043083", "names": ["Coronal synostosis, syndactyly and jejunal atresia", "coronal synostosis, syndactyly and jejunal atresia", "asymmetrical coronal synostosis, cutaneous syndactyly of the fingers and toes, and jejunal atresia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coronal synostosis, syndactyly and jejunal atresia", "shortest_name_length": 50}
{"curie": "MONDO:0016589", "names": ["PCCA", "progressive cerebello-cerebral atrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive cerebello-cerebral atrophy", "shortest_name_length": 4}
{"curie": "UMLS:C3489447", "names": ["Hyperkalemic Periodic Paralysis Type 2", "Hyperkaliemic Periodic Paralysis Type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyperkalemic Periodic Paralysis Type 2", "shortest_name_length": 38}
{"curie": "MONDO:0012622", "names": ["LBSL", "MITOCHONDRIAL ASPARTYL-tRNA SYNTHETASE DEFICIENCY", "Mitochondrial Aspartyl-tRNA Synthetase Deficiency", "mitochondrial aspartyl-tRNA synthetase deficiency", "leukoencephalopathy with brain stem and spinal cord involvement - high lactate", "leukoencephalopathy with brain stem and spinal cord involvement - lactate elevation", "Leucoencephalopathy with brainstem and spinal cord involvement and lactate elevation", "Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation", "Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation", "leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation", "LEUKOENCEPHALOPATHY WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LACTATE ELEVATION", "Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome", "leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome", "leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation", "Leukoencephalopathy with brain stem and spinal cord involvement and high lactate syndrome", "Leucoencephalopathy with brain stem and spinal cord involvement and high lactate syndrome", "leukoencephalopathy with brain stem and spinal cord involvement-lactate elevation syndrome", "Leukoencephalopathy with brain stem and spinal cord involvement-lactate elevation syndrome", "LBSL - Leucoencephalopathy with brainstem and spinal cord involvement with lactate elevation", "LBSL - Leukoencephalopathy with brainstem and spinal cord involvement with lactate elevation", "Leucoencephalopathy with brain stem and spinal cord involvement and lactate elevation syndrome", "Leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation syndrome", "Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation (disorder)", "Leukoencephalopathy with brain stem and spinal cord involvement and high lactate syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C5205699", "names": ["Head and Neck Neuroendocrine Carcinoma", "Primary Head and Neck Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Head and Neck Neuroendocrine Carcinoma", "shortest_name_length": 38}
{"curie": "MONDO:0017722", "names": ["Sandhoff disease, juvenile form", "juvenile GM2 gangliosidosis 0 variant", "Hexosaminidases A and B deficiency, juvenile form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sandhoff disease, juvenile form", "shortest_name_length": 31}
{"curie": "UMLS:C5447368", "names": ["Advanced Malignant Small Intestinal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Malignant Small Intestinal Neoplasm", "shortest_name_length": 44}
{"curie": "UMLS:C1336899", "names": ["Uterine Angiosarcoma", "Angiosarcoma of Uterus", "Uterine Hemangiosarcoma", "Hemangiosarcoma of Uterus", "Angiosarcoma of the Uterus", "Hemangiosarcoma of the Uterus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Angiosarcoma", "shortest_name_length": 20}
{"curie": "UMLS:C5555934", "names": ["Oral Cavity Carcinoma Cuniculatum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral Cavity Carcinoma Cuniculatum", "shortest_name_length": 33}
{"curie": "MONDO:0005195", "names": ["septic peritonitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "septic peritonitis", "shortest_name_length": 18}
{"curie": "UMLS:C1511105", "names": ["Benign Vaginal Melanocytic Nevus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Vaginal Melanocytic Nevus", "shortest_name_length": 32}
{"curie": "MONDO:0018892", "names": ["CAMS2", "wyburn-mason syndrome", "Wyburn-Mason syndrome", "Wyburn Mason syndrome", "wyburn-mason's syndrome", "Wyburn Mason's syndrome", "Wyburn-Mason's syndrome", "bonnet-Decaume-Blanc syndrome", "bonnet-Dechaume-Blanc syndrome", "Bonnet-Dechaume-Blanc syndrome", "Cerebral-retinal arteriovenous aneurysm", "Cerebral-retinal arteriovenous aneurysm syndrome", "Cerebral-retinal arteriovenous aneurysm (disorder)", "Cerebrofacial arteriovenous metameric syndrome type 2", "arteriovenous aneurysm of mid-brain and retina, facial nevi and mental changes", "Arteriovenous aneurysm of mid-brain and retina, facial nevi and mental changes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wyburn-Mason syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0012498", "names": ["CSNBAD1", "RHO congenital stationary night blindness", "rhodopsin-related congenital stationary night blindness", "night blindness, congenital stationary, rhodopsin-related", "Night Blindness, Congenital Stationary, Rhodopsin-Related", "NIGHT BLINDNESS, CONGENITAL STATIONARY, RHODOPSIN-RELATED", "congenital stationary night blindness autosomal dominant 1", "night blindness, congenital stationary, autosomal dominant 1", "Night Blindness, Congenital Stationary, Autosomal Dominant 1", "NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 1", "congenital stationary night blindness caused by mutation in RHO", "congenital stationary night blindness autosomal dominant type 1", "night blindness, congenital stationary, autosomal dominant type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital stationary night blindness autosomal dominant 1", "shortest_name_length": 7}
{"curie": "MONDO:0006487", "names": ["vaginal adenoid cystic cancer", "Vaginal Adenoid Cystic Cancer", "vaginal adenoid cystic carcinoma", "Vaginal Adenoid Cystic Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vaginal adenoid cystic carcinoma", "shortest_name_length": 29}
{"curie": "UMLS:C0281394", "names": ["AIDS Related Diffuse Small Cleaved Cell Lymphoma", "AIDS-Related Diffuse Small Cleaved Cell Lymphoma", "AIDS-related diffuse small cleaved cell lymphoma", "diffuse small cleaved cell lymphoma, AIDS-related", "AIDS Associated Diffuse Small Cleaved Cell Lymphoma", "AIDS associated diffuse small cleaved cell lymphoma", "AIDS-Associated Diffuse Small Cleaved Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Diffuse Small Cleaved Cell Lymphoma", "shortest_name_length": 48}
{"curie": "MONDO:0013202", "names": ["WS4C", "Waardenburg syndrome type 4C", "WAARDENBURG SYNDROME, TYPE 4C", "Waardenburg syndrome type IVC", "Waardenburg syndrome, type 4C", "Waardenburg Syndrome, Type 4c", "WAARDENBURG SYNDROME, TYPE IVC", "Waardenburg syndrome with Hirschsprung disease type 4C", "Waardenburg syndrome with Hirschsprung disease, type 4C", "WAARDENBURG SYNDROME WITH HIRSCHSPRUNG DISEASE, TYPE 4C", "Waardenburg Syndrome With Hirschsprung Disease, Type 4c Waardenburg Syndrome, Type Ivc"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Waardenburg syndrome type 4C", "shortest_name_length": 4}
{"curie": "MONDO:0003424", "names": ["Oncocytoma", "ONCOCYTOMA", "oncocytoma", "oncocytomas", "oxyphil adenoma", "Oxyphil adenoma", "oxyphilic adenoma", "Oxyphilic adenoma", "Oncocytic Adenoma", "Oncocytic adenoma", "oncocytic adenoma", "Oxyphilic Adenoma", "Adenoma, Oxyphilic", "hurthle cell tumor", "Hurthle Cell Tumor", "Hurthle cell tumor", "Hurthle cell tumour", "Huerthle Cell Tumor", "Hurthle cell; tumor", "tumor; Hurthle cell", "Hurthle cell adenoma", "hurthle cell adenoma", "Hurthle Cell Neoplasm", "hurthle cell neoplasm", "Hurthle cell neoplasm", "adenoma; Hurthle cell", "Hurthle cell; adenoma", "Huerthle cell adenoma", "cell hurthle neoplasms", "Hurthle cell neoplasm (thyroid)", "Thyroid Gland Oncocytic Neoplasm", "Follicular adenoma, oxyphilic cell", "follicular adenoma, oxyphilic cell", "Thyroid Gland Hurthle Cell Neoplasm", "Oxyphilic adenoma (morphologic abnormality)", "Thyroid Gland Hurthle (Oncocytic) Cell Tumor", "Hurthle cell neoplasm (morphologic abnormality)", "Thyroid Gland Hurthle (Oncocytic) Cell Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oncocytic adenoma", "shortest_name_length": 10}
{"curie": "UMLS:C5239574", "names": ["Refractory Nodal Peripheral T-Cell Lymphoma with TFH Phenotype"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Nodal Peripheral T-Cell Lymphoma with TFH Phenotype", "shortest_name_length": 62}
{"curie": "UMLS:C0856348", "names": ["Ethmoid Fracture", "ethmoid; fracture", "Fractured ethmoid", "fracture; ethmoid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fractured ethmoid", "shortest_name_length": 16}
{"curie": "UMLS:C0259756", "names": ["Herxheimer", "herxheimer reaction", "Herxheimer reaction", "herxheimer reactions", "Herxheimer; reaction", "reaction; Herxheimer", "Herxheimer's reaction", "Herxheimer's Reaction", "herxheimer's reaction", "Jarisch Herxheimer reaction", "Jarisch-Herxheimer reaction", "jarisch herxheimer reaction", "herxheimer jarisch reaction", "jarisch-herxheimer reaction", "JARISCH HERXHEIMER REACTION", "Jarisch Herxheimer reaction (disorder)", "Jarisch-Herxheimer reaction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jarisch Herxheimer reaction", "shortest_name_length": 10}
{"curie": "UMLS:C4726589", "names": ["Locally Advanced Bile Duct Cancer", "Locally Advanced Bile Duct Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Bile Duct Carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0014055", "names": ["FAME4", "FCMTE4", "familial adult myoclonic epilepsy 4", "epilepsy, familial ADULT myoclonic, 4", "EPILEPSY, FAMILIAL ADULT MYOCLONIC, 4", "epilepsy, familial adult myoclonic, 4", "epilepsy, myoclonic, familial adult, 4", "familial cortical myoclonic tremor and epilepsy 4", "CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 4", "cortical myoclonic tremor with epilepsy, familial, 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, familial adult myoclonic, 4", "shortest_name_length": 5}
{"curie": "UMLS:C4524748", "names": ["Postneoadjuvant Therapy Stage IIIB Gastroesophageal Junction Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postneoadjuvant Therapy Stage IIIB Gastroesophageal Junction Adenocarcinoma AJCC v8", "shortest_name_length": 83}
{"curie": "MONDO:0019876", "names": ["Invdupdel(8p)", "Inverted 8p duplication/deletion syndrome", "inverted 8p duplication/deletion syndrome", "8p inverted duplication deletion syndrome", "8p inverted duplication/deletion syndrome", "8p inverted duplication deletion syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "8p inverted duplication/deletion syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0009293", "names": ["GSD5", "GSD 5", "GSD V", "McArdle", "GSD type 5", "GSD type V", "Glycogenosis 5", "Glycogenosis 5s", "PYGM Deficiency", "McArdle disease", "McArdle Disease", "Mcardle disease", "PYGM DEFICIENCY", "Pygm deficiency", "mcardle disease", "MCARDLE DISEASE", "McArdles Disease", "McArdles disease", "Deficiency, PYGM", "disease mcardles", "Disease, McArdle", "mcardles disease", "Mcardle Syndrome", "McArdle's Disease", "Mcardle Syndromes", "Mcardle's Disease", "McArdle's disease", "PYGM Deficiencies", "mcardle's disease", "Syndrome, Mcardle", "Deficiencies, PYGM", "disease mcardles's", "Syndromes, Mcardle", "Disease, McArdle's", "Glycogenosis type V", "glycogenosis type 5", "Glycogenosis type 5", "type 5 glycogenosis", "glycogenosis type V", "Glycogenosis, type 5", "GLYCOGENOSIS, TYPE V", "Glycogen Storage Disease V", "Glycogen storage disease 5", "glycogen storage disease V", "GLYCOGEN STORAGE DISEASE V", "glycogen storage disease 5", "MYOPHOSPHORYLASE DEFICIENCY", "Myophosphorylase deficiency", "myophosphorylase deficiency", "deficiency, Myophosphorylase", "deficiency; myophosphorylase", "myophosphorylase; deficiency", "Myophosphorylase deficiencies", "PYGM glycogen storage disease", "deficiencies, Myophosphorylase", "McArdle-Schmid-Pearson disease", "Glycogen storage disease type V", "glycogen storage disease type v", "GLYCOGEN STORAGE DISEASE TYPE V", "Type V glycogen storage disease", "Glycogen Storage Disease Type 5", "Glycogen Storage Disease Type V", "glycogen storage disease type 5", "MUSCLE PHOSPHORYLASE DEFICIENCY", "Muscle Phosphorylase Deficiency", "glycogen storage disease type V", "Glycogen storage disease type 5", "muscle phosphorylase deficiency", "Phosphorylase Deficiency, Muscle", "glycogen storage disease, type V", "Deficiency, Muscle Phosphorylase", "Glycogen storage disease, type V", "Muscle Phosphorylase Deficiencies", "Phosphorylase Deficiencies, Muscle", "Deficiencies, Muscle Phosphorylase", "McArdle type glycogen storage disease", "McArdle Type Glycogen Storage Disease", "Muscle phosphorylase deficiency syndrome", "Myophosphorylase deficiency glycogenosis", "MUSCLE GLYCOGEN PHOSPHORYLASE DEFICIENCY", "muscle glycogen phosphorylase deficiency", "Muscle Glycogen Phosphorylase Deficiency", "MYOPHOSPHORYLASE DEFICIENCY GLYCOGENOSIS", "Muscle glycogen phosphorylase deficiency", "glycogen storage disease type V (diagnosis)", "Glycogen storage disease, type V (disorder)", "glycogen storage disease caused by mutation in PYGM", "GSD due to muscle glycogen phosphorylase deficiency", "glycogenosis due to muscle glycogen phosphorylase deficiency", "Glycogenosis due to muscle glycogen phosphorylase deficiency", "glycogen storage disease due to muscle glycogen phosphorylase deficiency", "Glycogen storage disease due to muscle glycogen phosphorylase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease V", "shortest_name_length": 4}
{"curie": "UMLS:C0522351", "names": ["VERTIGO POSTURAL", "Postural vertigo", "postural vertigo", "Positional Vertigo", "Positional vertigo", "Vertigo positional", "positional vertigo", "vertigo positional", "Vertigo, Positional", "Postural vertigo, NOS", "Positional vertigo, NOS", "Positional vertigo (finding)", "positional vertigo (symptom)", "Vertigo induced by motion of head or body", "Vertigo induced by position of head or body", "spinning dizziness with sudden changes in position"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Positional Vertigo", "shortest_name_length": 16}
{"curie": "UMLS:C0342898", "names": ["ApoA-I deficiency", "Familial apoA-I deficiency", "apolipoprotein A-I deficiency", "Apolipoprotein A-I deficiency", "APOLIPOPROTEIN A-I DEFICIENCY", "Familial hypoalphalipoproteinemia", "Apolipoprotein A-I deficiency (disorder)", "apolipoprotein A-I deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Apolipoprotein A-I deficiency", "shortest_name_length": 17}
{"curie": "MONDO:0019335", "names": ["mHPA", "mild HPA", "non-PKU HPA", "mild hyperphenylalaninemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mild hyperphenylalaninemia", "shortest_name_length": 4}
{"curie": "MONDO:0017285", "names": ["Prepenile scrotum", "Penoscrotal transposition", "Penoscrotal Transposition", "penoscrotal transposition", "penoscrotal transposition (disease)", "Congenital penoscrotal transposition", "congenital penoscrotal transposition", "Congenital Penoscrotal Transposition", "congenital transposition of the penis", "Congenital transposition of the penis", "Congenital penoscrotal transposition (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "penoscrotal transposition", "shortest_name_length": 17}
{"curie": "MONDO:0002359", "names": ["Periosteal Chondroma", "periosteal chondroma", "Periosteal chondroma", "juxtacortical chondroma", "Juxtacortical Chondroma", "Juxtacortical chondroma", "juxtacortical chondroma (morphologic abnormality)", "Juxtacortical chondroma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "periosteal chondroma", "shortest_name_length": 20}
{"curie": "UMLS:C0877275", "names": ["Spinal cord infection", "cord infection spinal", "spinal cord infection", "infection spinal cord", "cord infections spinal", "spinal cord; infection", "infection; spinal cord"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spinal cord infection", "shortest_name_length": 21}
{"curie": "MONDO:0005405", "names": ["Childhood asthma", "asthma childhood", "pediatric asthma", "childhood asthma", "ASTHMA CHILDHOOD", "Pediatric asthma", "Childhood Asthma", "asthma; childhood", "childhood; asthma", "Asthma, childhood", "Asthma in children", "Asthma in Children", "asthma of childhood", "Childhood asthma NOS", "childhood-onset asthma", "childhood onset asthma", "Childhood asthma (disorder)", "childhood asthma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood onset asthma", "shortest_name_length": 16}
{"curie": "MONDO:0000940", "names": ["Trypanosomosis", "trypanosomiasis", "Trypanosomiasis", "Trypanosomiases", "Trypanosomiasis NOS", "Trypanosomiasis (disorder)", "trypanosomiasis (diagnosis)", "Trypanosomiasis, unspecified", "Trypanosoma infectious disease", "Trypanosoma disease or disorder", "Trypanosoma caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trypanosomiasis", "shortest_name_length": 14}
{"curie": "UMLS:C4330901", "names": ["Oropharyngeal (p16-Negative) Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oropharyngeal (p16-Negative) Carcinoma by AJCC v8 Stage", "shortest_name_length": 55}
{"curie": "MONDO:0004111", "names": ["refractory hematologic cancer", "Refractory Hematologic Cancer", "refractory hematologic malignancy", "Refractory Hematologic Malignancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "refractory hematologic cancer", "shortest_name_length": 29}
{"curie": "MONDO:0002089", "names": ["Retinal vasc. occlusion", "retinal vascular occlusion", "Retinal Vascular Occlusion", "Retinal vascular occlusion", "occlusion; retinal vessels", "retinal vascular occlusions", "Retinal vascular occlusions", "Retinal vascular occlusion, NOS", "Retinal vascular occlusion (disorder)", "retinal vascular occlusion (diagnosis)", "Unspecified retinal vascular occlusion", "Retinal vascular occlusion, unspecified", "retinal vascular occlusion, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal vascular occlusion", "shortest_name_length": 23}
{"curie": "MONDO:0002727", "names": ["disorder of 1st nerve", "Disorder of 1st Nerve", "Disorders of 1st nerve", "n.olfactorius; disorder", "Olfactory Nerve Disease", "olfactory nerve disease", "Cranial Nerve I Diseases", "olfactory nerve disorder", "Olfactory nerve disorder", "Olfactory Nerve Diseases", "Olfactory Nerve Disorder", "disorder olfactory nerve", "disorder of the 1st nerve", "Cranial Nerve I Disorders", "Disorder of the 1st Nerve", "disorder; olfactory nerve", "Olfactory nerve disorders", "disease of olfactory nerve", "disorder of olfactory nerve", "Disorder of cranial nerve 1", "Disorder of olfactory nerve", "Disorders of olfactory nerve", "First cranial nerve disorder", "Disorders of the first nerve", "First Cranial Nerve Diseases", "Disorder of olfactory nerve, NOS", "disorder of olfactory [1st] nerve", "Disorders of olfactory (1st) nerve", "olfactory nerve disease or disorder", "Olfactory nerve disease or syndrome", "Disorder of the first cranial nerve", "disease or disorder of olfactory nerve", "Disorder of olfactory nerve (disorder)", "disease (or disorder); olfactory nerve", "First cranial nerve disease or syndrome", "disorder of olfactory nerve (diagnosis)", "Disorder of the first cranial nerve, NOS", "disease (or disorder); cranial nerve, first"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "olfactory nerve disorder", "shortest_name_length": 21}
{"curie": "UMLS:C5421217", "names": ["Visual Pathway Medulloepithelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Visual Pathway Medulloepithelioma", "shortest_name_length": 33}
{"curie": "UMLS:C5206774", "names": ["Recurrent Kidney Medullary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Kidney Medullary Carcinoma", "shortest_name_length": 36}
{"curie": "UMLS:C0341117", "names": ["esophageal erosion", "erosion; esophagus", "esophagus; erosion", "Esophageal erosion", "oesophageal erosion", "esophageal erosions", "Esophageal erosions", "Oesophageal erosion", "Erosion of esophagus", "Oesophageal erosions", "esophageal erosion (diagnosis)", "Esophageal erosions (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal erosions", "shortest_name_length": 18}
{"curie": "UMLS:C2609043", "names": ["Pheochromocytoma crisis", "Phaeochromocytoma crisis", "Pheochromocytoma crisis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pheochromocytoma crisis", "shortest_name_length": 23}
{"curie": "MONDO:0014069", "names": ["WAHAB SYNDROME", "WAHAB syndrome", "Wahab syndrome", "CAMPTODACTYLY, CLINODACTYLY, SYNDACTYLY, AND BIFID TOE SYNDROME", "camptodactyly, clinodactyly, syndactyly, and bifid toe syndrome", "syndactyly-camptodactyly and clinodactyly of fifth fingers-bifid toes syndrome", "Syndactyly-camptodactyly and clinodactyly of fifth fingers-bifid toes syndrome", "Syndactyly, camptodactyly and clinodactyly of fifth fingers, bifid toes syndrome", "Synactyly-camptodactyly and clinodactyly of fifth fingers-bifid halluces syndrome", "Synactyly, camptodactyly and clinodactyly of fifth fingers, bifid halluces syndrome", "Syndactyly, camptodactyly and clinodactyly of fifth fingers, bifid toes syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndactyly-camptodactyly and clinodactyly of fifth fingers-bifid toes syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C4524898", "names": ["stage IIIC anal cancer", "Stage IIIC Anal Cancer", "Stage IIIC Anal Cancer AJCC v8", "stage IIIC anal cancer AJCC v8", "Stage IIIC Anal Carcinoma AJCC v8", "stage IIIC anal carcinoma AJCC v8", "Stage IIIC Anal Canal and Perianal (Anal Margin) Carcinoma AJCC v8", "stage IIIC anal canal and perianal (anal margin) carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Anal Cancer AJCC v8", "shortest_name_length": 22}
{"curie": "UMLS:C2984069", "names": ["Vulvar Cancer by AJCC v7 Stage", "Vulvar Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Cancer by AJCC v7 Stage", "shortest_name_length": 30}
{"curie": "UMLS:C4683740", "names": ["Stage IA Mycosis Fungoides and Sezary Syndrome AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Mycosis Fungoides and Sezary Syndrome AJCC v8", "shortest_name_length": 54}
{"curie": "MONDO:0006712", "names": ["cornea edema", "CORNEAL EDEMA", "cornea; edema", "Corneal edema", "Corneal Edema", "corneal edema", "edema corneal", "edema; cornea", "CORNEAL OEDEMA", "corneal oedema", "Edema, Corneal", "Corneal Edemas", "Corneal oedema", "Edema of cornea", "Edemas, Corneal", "Oedema of cornea", "Corneal edema, NOS", "Corneal oedema, NOS", "Corneal edema (disorder)", "Unspecified corneal edema", "corneal edema (diagnosis)", "Corneal edema, unspecified", "Corneal oedema, unspecified", "corneal edema (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal edema", "shortest_name_length": 12}
{"curie": "UMLS:C0281779", "names": ["anal condyloma", "ANAL CONDYLOMA", "Condyloma anal", "Anal Condyloma", "Anal Condylomata", "anal condylomata", "ANAL CONDYLOMATA", "Condylomata of Anus", "Condylomata of the Anus", "Anal Condyloma Acuminatum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Condyloma anal", "shortest_name_length": 14}
{"curie": "MONDO:0020851", "names": ["SPGF30", "SPERMATOGENIC FAILURE 30", "spermatogenic failure 30"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 30", "shortest_name_length": 6}
{"curie": "UMLS:C5206668", "names": ["Penile Schwannoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Penile Schwannoma", "shortest_name_length": 17}
{"curie": "MONDO:0004104", "names": ["spleen hairy cell leukemia", "Hairy cell leukemia of spleen", "hairy cell leukemia of spleen", "hairy cell leukaemia of spleen", "Hairy cell leukaemia of spleen", "Leukemic reticuloendotheliosis, spleen", "Leukemic reticuloendotheliosis of spleen", "Hairy cell leukemia of spleen (disorder)", "hairy cell leukemia of spleen (diagnosis)", "Leukaemic reticuloendotheliosis of spleen", "splenic manifestation of hairy cell leukemia", "Splenic Manifestation of Hairy Cell Leukemia", "splenic manifestation of hairy cell leukaemia", "Leukemic reticuloendotheliosis involving spleen", "Leukaemic reticuloendotheliosis involving spleen"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "splenic manifestation of hairy cell leukemia", "shortest_name_length": 26}
{"curie": "MONDO:0032742", "names": ["IIAE9", "ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 9", "encephalopathy, acute, infection-induced, susceptibility to, 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephalopathy, acute, infection-induced, susceptibility to, 9", "shortest_name_length": 5}
{"curie": "UMLS:C4528622", "names": ["Stage IIIB Vulvar Cancer", "Stage IIIB Vulvar Cancer AJCC v8", "Stage IIIB Vulvar Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Vulvar Cancer AJCC v8", "shortest_name_length": 24}
{"curie": "MONDO:0020374", "names": ["CCA1", "CTRCT7", "CATARACT 7", "Blue-dot cataract", "Blue dot cataract", "Cerulean cataract", "blue-dot cataract", "cerulean cataract", "cataract; blue dot", "blue dot; cataract", "cataract; cerulean", "cerulean; cataract", "blue; dot cataract", "dot cataract; blue", "CATARACT 7, CERULEAN TYPE", "cerulean; cerulean cataract", "Congenital blue dot cataract", "congenital blue dot cataract", "Cataract, congenital cerulean", "Cataract, congenital, cerulean", "Cataracts, congenital, cerulean", "cataract, congenital, blue dot type 1", "cataract, congenital, cerulean type 1", "Cataract, congenital, cerulean type 1", "Cataract, congenital, blue dot type 1", "Cataract, Congenital, Blue Dot Type, 1", "Cataract, Congenital, Cerulean Type, 1", "CATARACT, CONGENITAL, CERULEAN TYPE, 1", "Congenital blue dot cataract (disorder)", "congenital blue dot cataract (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerulean cataract", "shortest_name_length": 4}
{"curie": "UMLS:C1706924", "names": ["Benign Outer Hair Sheath and Infundibulum Tumor", "Benign Outer Hair Sheath and Infundibulum Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Outer Hair Sheath and Infundibulum Neoplasm", "shortest_name_length": 47}
{"curie": "MONDO:0012311", "names": ["Spondylomegaepiphyseal Dysplasia With Upper Limb Mesomelia, Punctate Calcifications, And Deafness", "spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctate calcifications, and deafness", "SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATE CALCIFICATIONS, AND DEAFNESS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctate calcifications, and deafness", "shortest_name_length": 97}
{"curie": "MONDO:0013473", "names": ["HCAD", "Hirschsprung disease, CARDIAC defects, and autonomic dysfunction", "Hirschsprung disease, cardiac defects, and autonomic dysfunction", "HIRSCHSPRUNG DISEASE, CARDIAC DEFECTS, AND AUTONOMIC DYSFUNCTION", "Hirschsprung Disease, Cardiac Defects, and Autonomic Dysfunction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hirschsprung disease, cardiac defects, and autonomic dysfunction", "shortest_name_length": 4}
{"curie": "UMLS:C0677932", "names": ["progressive disease", "Progressive Neoplastic Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Progressive Neoplastic Disease", "shortest_name_length": 19}
{"curie": "MONDO:0012088", "names": ["CILD5", "primary ciliary dyskinesia 5", "ciliary dyskinesia, primary, 5", "CILIARY DYSKINESIA, PRIMARY, 5", "Ciliary Dyskinesia, Primary, 5", "HYDIN primary ciliary dyskinesia", "primary ciliary dyskinesia type 5", "ciliary dyskinesia, primary, type 5", "primary ciliary dyskinesia 5 without situs inversus", "primary ciliary dyskinesia caused by mutation in HYDIN", "CILIARY DYSKINESIA, PRIMARY, 5, WITHOUT SITUS INVERSUS", "ciliary dyskinesia, primary, 5, without situs inversus", "Ciliary Dyskinesia, Primary, 5, with or without Situs Inversus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia 5", "shortest_name_length": 5}
{"curie": "MONDO:0015055", "names": ["AAE 2", "AAE II", "acquired angioedema type 2", "acquired angioneurotic edema type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired angioedema type 2", "shortest_name_length": 5}
{"curie": "MONDO:0030309", "names": ["LHONAR", "MC1DN38", "mitochondrial complex 1 deficiency, nuclear type 38", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 38", "Leber hereditary optic neuropathy, autosomal recessive", "LEBER HEREDITARY OPTIC NEUROPATHY, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leber hereditary optic neuropathy, autosomal recessive", "shortest_name_length": 6}
{"curie": "MONDO:0003004", "names": ["Maculopathy", "Maculopathies", "Macular Dystrophy", "Dystrophy, Macular", "Macular Dystrophies", "macular degeneration", "Degeneration macular", "MACULAR DEGENERATION", "Degeneration;macular", "Macular Degeneration", "DEGENERATION MACULAR", "degeneration macular", "Macular degeneration", "Macular Degenerations", "macular degenerations", "Degeneration, Macular", "degeneration of macula", "MACULA LUTEA DEGENERATION", "Macula lutea degeneration", "macula lutea degeneration", "Macular luteal degeneration", "macula retinal degeneration", "Macular degeneration syndrome", "macular degeneration of retina", "Macular degeneration of retina", "Pigmented macular degeneration", "Degenerative disorder of macula", "degenerative disorder of macula", "macular degeneration (diagnosis)", "macula lutea retinal degeneration", "Retinal macula lutea degeneration", "retinal degeneration of macula lutea", "macular degeneration (physical finding)", "Degenerative disorder of macula (disorder)", "Macular degeneration of retina, unspecified", "degenerative disorder of macula (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macular degeneration", "shortest_name_length": 11}
{"curie": "UMLS:C1275687", "names": ["HZV keratitis", "Varicella keratitis", "varicella keratitis", "herpes zoster keratitis", "Herpes zoster keratitis", "varicella keratitis (diagnosis)", "Herpes zoster keratitis (disorder)", "herpes zoster keratitis (diagnosis)", "herpes; keratitis, h.zoster (etiology)", "keratitis; herpes virus, zoster (etiology)", "herpes virus; keratitis, zoster (etiology)", "herpes; keratitis, h.zoster (manifestation)", "keratitis; herpes virus, zoster (manifestation)", "herpes virus; keratitis, zoster (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Herpes zoster keratitis", "shortest_name_length": 13}
{"curie": "MONDO:0010128", "names": ["Thyrocerebrorenal syndrome", "thyrocerebrorenal syndrome", "cutler-Bass-Romshe syndrome", "Cutler Bass Romshe syndrome", "Cutler-Bass-Romshe syndrome", "THYROCEREBRORETINAL syndrome", "THYROCEREBRORETINAL SYNDROME", "Thyrocerebroretinal syndrome", "Thyrocerebral-retinal syndrome", "Thyrocerebrorenal syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyrocerebrorenal syndrome", "shortest_name_length": 26}
{"curie": "MONDO:0011071", "names": ["FPDMM", "FPDAML", "FPD/AML", "FPS/AML", "Platelet Disorder, Aspirin-Like", "PLATELET DISORDER, ASPIRIN-LIKE", "Familial Platelet Disorder and AML Syndrome", "Familial platelet disorder with associated myeloid malignancy", "Familial Platelet Disorder with Associated Myeloid Malignancy", "PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY", "Platelet Disorder, Familial, with Associated Myeloid Malignancy", "Familial platelet disorder with predisposition to myeloid malignancy", "Familial platelet disorder with propensity to acute myeloid leukemia", "Familial thrombocytopenia with propensity to acute myelogenous leukemia", "THROMBOCYTOPENIA, FAMILIAL, WITH PROPENSITY TO ACUTE MYELOGENOUS LEUKEMIA", "Thrombocytopenia, Familial, with Propensity to Acute Myelogenous Leukemia", "hereditary thrombocytopenia and hematologic cancer predisposition syndrome", "Familial platelet disorder with predisposition to acute myelogenous leukemia", "Familial platelet syndrome with predisposition to acute myelogenous leukemia", "Familial platelet syndrome with predisposition to acute myelogenous leukaemia", "Familial platelet syndrome with predisposition to acute myelogenous leukemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary thrombocytopenia and hematologic cancer predisposition syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0018513", "names": ["Colon Squamous Cell Cancer", "Colon Epidermoid Carcinoma", "colon epidermoid carcinoma", "colon squamous cell cancer", "colonic epidermoid carcinoma", "Colonic Epidermoid Carcinoma", "Colonic Epidermoid carcinoma", "Colon Squamous Cell Carcinoma", "colon squamous cell carcinoma", "epidermoid carcinoma of colon", "Epidermoid Carcinoma of Colon", "Squamous Cell Colon Carcinoma", "squamous cell colon carcinoma", "Colonic Squamous Cell Carcinoma", "colonic squamous cell carcinoma", "Squamous cell carcinoma of colon", "squamous cell carcinoma of colon", "Squamous Cell Carcinoma of Colon", "epidermoid carcinoma of the colon", "Epidermoid Carcinoma of the Colon", "Squamous cell carcinoma of the colon", "Squamous Cell Carcinoma of the Colon", "squamous cell carcinoma of the colon", "Squamous cell carcinoma of colon (disorder)", "Squamous cell carcinoma of colon (diagnosis)", "large intestine malignant carcinoma of colon squamous cell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "squamous cell carcinoma of colon", "shortest_name_length": 26}
{"curie": "UMLS:C0276754", "names": ["Onychomycosis due to Trichophyton rubrum", "Onychomycosis caused by Trichophyton rubrum", "Onychomycosis caused by Trichophyton rubrum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Onychomycosis due to Trichophyton rubrum", "shortest_name_length": 40}
{"curie": "UMLS:C2586211", "names": ["thrombosis", "Vascular Thrombosis", "Vascular thrombosis", "Thrombosis of blood vessel", "thrombosis of blood vessel", "Thrombosis of blood vessel (disorder)", "thrombosis of blood vessel (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thrombosis of blood vessel", "shortest_name_length": 10}
{"curie": "MONDO:0003442", "names": ["bladder papillary urothelial neoplasm", "Bladder Papillary Urothelial Neoplasm", "bladder papillary transitional cell neoplasm", "Bladder Papillary Transitional Cell Neoplasm", "urinary bladder papillary urothelial neoplasm", "Urinary Bladder Papillary Urothelial Neoplasm", "urinary bladder Papillary Urothelial neoplasm", "Urinary Bladder Papillary Transitional Cell Neoplasm", "urinary bladder papillary transitional cell neoplasm", "urinary bladder urothelium papillary epithelial neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder papillary urothelial neoplasm", "shortest_name_length": 37}
{"curie": "MONDO:0008171", "names": ["CAON", "kidney stone", "Renal stones", "Kidney Stone", "Kidney stones", "Renal calculi", "renal calculi", "Renal Calculi", "kidney stones", "Renal lithiasis", "renal lithiasis", "Nephrolithiasis", "lithiasis renal", "NEPHROLITHIASIS", "nephrolithiasis", "calculus of kidney", "CALCULUS DISORDERS", "Nephrolithiasis NOS", "Nephrolithiasis, NOS", "Stone - kidney/ureter", "nephrolithiasis (diagnosis)", "Calculus of kidney and ureter", "urolithiasis, calcium oxalate", "calculus of kidney and ureter", "nephrolithiasis, calcium oxalate", "calculus; ureter, with calculus kidney", "ureter; calculus, with calculus, kidney", "Calculus of kidney and ureter (disorder)", "calculus of kidney and ureter (diagnosis)", "Calculus of kidney with calculus of ureter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrolithiasis", "shortest_name_length": 4}
{"curie": "UMLS:C0005700", "names": ["explosion", "blast injury", "Blast injury", "Blast Injury", "blast; injury", "Injury, Blast", "injury; blast", "Explosion NOS", "Blast injuries", "blast injuries", "Blast Injuries", "Injuries, Blast", "Explosion injury", "Blast injury, NOS", "Injury due to explosion", "Blast injury from explosion", "Explosion air pressure effects", "Injury due to explosion (disorder)", "Blast injury (morphologic abnormality)", "Effects of air pressure caused by explosion", "Effects of air pressure caused by explosion (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Blast Injuries", "shortest_name_length": 9}
{"curie": "MONDO:0015290", "names": ["Neurotrophic keratitis", "Anesthetic keratopathy", "neurotrophic keratitis", "Anaesthetic keratopathy", "Neurotrophic keratopathy", "neurotrophic keratopathy", "Neuroparalytic keratopathy", "Neurotrophic keratitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurotrophic keratopathy", "shortest_name_length": 22}
{"curie": "MONDO:0003769", "names": ["Herpetic Gastritis", "herpetic gastritis", "Herpesviridae viral gastritis", "Herpesviridae caused viral gastritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "herpetic gastritis", "shortest_name_length": 18}
{"curie": "UMLS:C0271308", "names": ["allergic blepharitis", "Blepharitis allergic", "Allergic blepharitis", "Eyelid contact eczema", "Contact eczema eyelid", "Contact allergy eyelid", "Allergic dermatitis eyelid", "contact dermatitis eyelids", "Contact dermatitis of eyelid", "contact dermatitis of eyelid", "Allergic dermatitis of eyelid", "Contact dermatitis of eyelid (disorder)", "contact dermatitis of eyelid (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Contact dermatitis of eyelid", "shortest_name_length": 20}
{"curie": "UMLS:C0334627", "names": ["Hodgkin; nodular sclerosis, cellular phase", "nodular sclerosis Hodgkin lymphoma, cellular phase", "Hodgkin's disease nodular sclerosis cellular phase", "Nodular Sclerosis Hodgkin Lymphoma, Cellular Phase", "Hodgkin disease, nodular sclerosis - cellular phase", "Hodgkin's Disease Nodular Sclerosis, Cellular Phase", "Hodgkin lymphoma, nodular sclerosis, cellular phase", "Hodgkin's disease, nodular sclerosis, cellular phase", "disease; Hodgkin's, nodular sclerosis, cellular phase", "Hodgkin's disease, nodular sclerosis - cellular phase", "[M]Hodgkin's disease, nodular sclerosis, cellular phase", "Nodular Sclerosis Classic Hodgkin Lymphoma, Cellular Phase", "Nodular Sclerosis Classical Hodgkin Lymphoma, Cellular Phase", "Classical Hodgkin lymphoma, nodular sclerosis, cellular phase", "nodular sclerosis Hodgkin lymphoma, cellular phase (diagnosis)", "Hodgkin's disease, nodular sclerosis - cellular phase (disorder)", "Hodgkin lymphoma, nodular sclerosis, cellular phase (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin lymphoma, nodular sclerosis, cellular phase", "shortest_name_length": 42}
{"curie": "MONDO:0010936", "names": ["Dmt1", "FTD3", "Dtm1", "Ftd3", "Ftd-3", "ALS17", "FTDALS7", "Ftd-Chmp2b", "ALS17, FORMERLY", "ALS17 (diagnosis)", "dementia, familial nonspecific", "Dementia, Familial Nonspecific", "amyotrophic lateral sclerosis ALS17", "CHMP2B amyotrophic lateral sclerosis", "amyotrophic lateral sclerosis type 17", "Chmp2b-Related Frontotemporal Dementia", "CHMP2B-related frontotemporal dementia", "AMYOTROPHIC LATERAL SCLEROSIS 17, FORMERLY", "chromosome 3-linked frontotemporal dementia", "Chromosome 3-Linked Frontotemporal Dementia", "Chromosome 3-linked frontotemporal dementia", "FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED", "CHMP2B-related amyotrophic lateral sclerosis", "frontotemporal dementia, chromosome 3-linked", "Frontotemporal Dementia, Chromosome 3-Linked", "AMYOTROPHIC LATERAL SCLEROSIS, CHMP2B-RELATED", "Amyotrophic Lateral Sclerosis, Chmp2B-Related", "amyotrophic lateral sclerosis, Chmp2B-related", "Frontotemporal dementia with gene located on 3p11", "[OBSOLETE] Amyotrophic Lateral Sclerosis, Chmp2B-Related", "amyotrophic lateral sclerosis caused by mutation in CHMP2B", "Frontotemporal dementia with gene located on 3p11 (disorder)", "Frontotemporal dementia with gene located on 3p11 (diagnosis)", "FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 7", "frontotemporal dementia and/or amyotrophic lateral sclerosis 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontotemporal dementia and/or amyotrophic lateral sclerosis 7", "shortest_name_length": 4}
{"curie": "MONDO:0014282", "names": ["SPG72", "hereditary spastic paraplegia 72", "Autosomal spastic paraplegia type 72", "autosomal spastic paraplegia type 72", "hereditary spastic paraplegia type 72", "REEP2 pure hereditary spastic paraplegia", "SPASTIC PARAPLEGIA 72, AUTOSOMAL DOMINANT", "spastic paraplegia 72, autosomal dominant", "SPASTIC PARAPLEGIA 72, AUTOSOMAL RECESSIVE", "spastic paraplegia 72, autosomal recessive", "Autosomal spastic paraplegia type 72 (disorder)", "pure hereditary spastic paraplegia caused by mutation in REEP2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 72", "shortest_name_length": 5}
{"curie": "MONDO:0043512", "names": ["TBI", "brain trauma", "Brain Trauma", "brain traumas", "Brain Traumas", "Trauma, Brain", "Traumas, Brain", "Traumatic Brain Injury", "traumatic brain damage", "Injury;brain;traumatic", "Traumatic brain damage", "brain damage traumatic", "traumatic brain injury", "brain injury traumatic", "Traumatic brain injury", "postconcussion syndrome", "Brain Injury, Traumatic", "post-traumatic dementia", "Post-Concussive Symptom", "POSTCONCUSSIVE SYNDROME", "Post-Concussion Symptom", "Postconcussion syndrome", "Post-traumatic dementia", "postconcussive syndrome", "Post Concussion Syndrome", "Post-concussion syndrome", "post concussion syndrome", "post concussion symptoms", "concussion post syndrome", "post concussive syndrome", "Brain Injury (Traumatic)", "POST CONCUSSIVE SYNDROME", "traumatic brain injuries", "Post-Concussive Symptoms", "Post-Concussion Syndrome", "postcontusional syndrome", "post syndrome concussion", "Traumatic Brain Injuries", "Post concussion syndrome", "brain injuries traumatic", "traumatic encephalopathy", "Traumatic encephalopathy", "Injury, Brain, Traumatic", "post-concussion syndrome", "Traumatic Encephalopathy", "Post Concussion Symptoms", "Post Concussive Symptoms", "Post-Concussive Syndrome", "Post-Concussion Symptoms", "post-concussive syndrome", "Post Concussive Syndrome", "Encephalopathy, Traumatic", "Post-contusional syndrome", "postconcussional syndrome", "Postconcussional syndrome", "encephalopathy; traumatic", "Post-Concussive Syndromes", "head injury with dementia", "traumatic; encephalopathy", "postcontusional; syndrome", "syndrome; postcontusional", "Brain Injuries, Traumatic", "POSTCONCUSSIONAL SYNDROME", "concussions post syndrome", "post-concussional syndrome", "Post-concussional syndrome", "Traumatic brain injury NOS", "post concussional syndrome", "brain injury due to trauma", "disorder; postconcussional", "syndrome; postconcussional", "Traumatic Encephalopathies", "postconcussional; disorder", "postconcussional; syndrome", "Dementia Due to Head Trauma", "Dementia due to head trauma", "dementia due to head trauma", "Encephalopathies, Traumatic", "TBI (Traumatic Brain Injury)", "TBI (traumatic brain injury)", "Postconcussion syndrome, NOS", "Traumatic brain injury (TBI)", "BRAIN SYNDROME, POSTTRAUMATIC", "post-traumatic brain syndrome", "Post-traumatic brain syndrome", "brain syndrome; post-traumatic", "TBI (Traumatic Brain Injuries)", "post-traumatic; brain syndrome", "TBIs (Traumatic Brain Injuries)", "Post-contusional encephalopathy", "Traumatic brain injury (disorder)", "traumatic brain damage (diagnosis)", "Post-traumatic dementia (disorder)", "Postconcussion syndrome (disorder)", "traumatic brain injury (diagnosis)", "postconcussion syndrome (diagnosis)", "head injury with dementia (diagnosis)", "Nonpsychotic post-traumatic brain syndrome", "Post-traumatic brain syndrome, nonpsychotic", "syndrome; brain, post-traumatic, nonpsychotic", "brain; syndrome, post-traumatic, nonpsychotic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "traumatic encephalopathy", "shortest_name_length": 3}
{"curie": "UMLS:C0153677", "names": ["Mediastinal metastases", "mediastinal metastases", "mediastinal metastasis", "Mediastinal metastasis", "Metastases to Mediastinum", "Metastasis to mediastinum", "Metastasis to the Mediastinum", "Metastases to the Mediastinum", "Metastases to the mediastinum", "Cancer metastatic to mediastinum", "Metastatic Tumor to the Mediastinum", "Metastatic Neoplasm to the Mediastinum", "Secondary malignant tumor of mediastinum", "Secondary malignant tumour of mediastinum", "Secondary malignant neoplasm of mediastinum", "secondary malignant neoplasm of mediastinum", "Metastatic malignant neoplasm of mediastinum", "Metastatic malignant neoplasm to mediastinum", "metastasis of malignant neoplasm to mediastinum", "Secondary malignant neoplasm of mediastinum, NOS", "Metastatic Malignant Neoplasm in the Mediastinum", "Metastatic Malignant Neoplasm to the Mediastinum", "Metastatic malignant neoplasm to mediastinum, NOS", "Metastatic malignant neoplasm to mediastinum (disorder)", "secondary malignant neoplasm of mediastinum (diagnosis)", "metastasis of malignant neoplasm to mediastinum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to mediastinum", "shortest_name_length": 22}
{"curie": "UMLS:C0347021", "names": ["Metastasis to choroid", "Secondary choroidal tumor", "Secondary choroidal tumour", "Cancer metastatic to choroid", "Metastatic Tumor to the Choroid", "Metastatic Neoplasm to the Choroid", "secondary malignant choroid neoplasm", "malignant choroid neoplasm secondary", "Secondary malignant neoplasm of choroid", "secondary malignant neoplasm of choroid", "Metastatic malignant neoplasm of choroid", "Metastatic malignant neoplasm to choroid", "Metastatic Malignant Neoplasm in the Choroid", "Metastatic Malignant Neoplasm to the Choroid", "secondary malignant neoplasm of choroid (diagnosis)", "Metastatic malignant neoplasm to choroid (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to choroid", "shortest_name_length": 21}
{"curie": "MONDO:0018323", "names": ["HSD10 disease, neonatal type", "MHBD deficiency, neonatal type", "HSD10 deficiency, neonatal type", "2-methyl-3-hydroxybutyric aciduria, neonatal type", "2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency, neonatal type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HSD10 disease, neonatal type", "shortest_name_length": 28}
{"curie": "MONDO:0005021", "names": ["DCM", "dilated cardiomyopathy", "Dilated Cardiomyopathy", "Dilated cardiomyopathy", "CARDIOMYOPATHY DILATED", "cardiomyopathy dilated", "Cardiomyopathy, dilated", "Cardiomyopathy, Dilated", "Dilated Cardiomyopathies", "Congestive Cardiomyopathy", "Cardiomyopathy;congestive", "cardiomyopathy congestive", "congestive cardiomyopathy", "Cardiomyopathies, Dilated", "Congestive cardiomyopathy", "Cardiomyopathy, congestive", "DCM - Dilated cardiomyopathy", "primary dilated cardiomyopathy", "Primary dilated cardiomyopathy", "Familial dilated cardiomyopathy", "familial dilated cardiomyopathy", "CCM - Congestive cardiomyopathy", "COCM - Congestive cardiomyopathy", "Congestive dilated cardiomyopathy", "heart; dilatation, cardiomyopathy", "Idiopathic dilation cardiomyopathy", "dilated cardiomyopathy (diagnosis)", "idiopathic dilation cardiomyopathy", "Stretched and thinned heart muscle", "Congestive (dilated) cardiomyopathy", "Congestive cardiomyopathy (disorder)", "congestive cardiomyopathy (diagnosis)", "cardiomyopathy; cardiomyopathy, dilated", "Primary dilated cardiomyopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy", "shortest_name_length": 3}
{"curie": "MONDO:0012003", "names": ["DFNB39", "autosomal recessive deafness 39", "Deafness, Autosomal Recessive 39", "DEAFNESS, AUTOSOMAL RECESSIVE 39", "deafness, autosomal recessive 39", "deafness, autosomal recessive type 39", "DEAFNESS, AUTOSOMAL RECESSIVE 39 (disorder)", "autosomal recessive nonsyndromic deafness 39", "HGF autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 39", "autosomal recessive nonsyndromic deafness type 39", "autosomal recessive nonsyndromic deafness caused by mutation in HGF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 39", "shortest_name_length": 6}
{"curie": "UMLS:C5418570", "names": ["Resectable Skin Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Skin Squamous Cell Carcinoma", "shortest_name_length": 39}
{"curie": "UMLS:C3805076", "names": ["Noninfective encephalitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Noninfective encephalitis", "shortest_name_length": 25}
{"curie": "MONDO:0017484", "names": ["femoral agenesis/hypoplasia, unilateral", "femoral intercalary meromelia, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "femoral agenesis/hypoplasia, unilateral", "shortest_name_length": 39}
{"curie": "MONDO:0007652", "names": ["Ménétrier", "Ménétrier Disease", "MENETRIER DISEASE", "Menetrier disease", "disease menetrier", "Ménétrier disease", "Menetrier Disease", "MENETRIER disease", "menetrier disease", "Disease, Menetrier", "Menetriers Disease", "disease menetriers", "menetrier's disease", "Ménétrier's disease", "Menetrier's Disease", "Menetrier's disease", "MENETRIER'S DISEASE", "Gastric hyperplasia", "Disease, Menetrier's", "Giant rugal gastritis", "gastritis hypertrophic", "Hypertrophic Gastritis", "hypertrophic gastritis", "Hypertrophic gastritis", "GASTRITIS HYPERTROPHIC", "Gastritis hypertrophic", "Gastritis, Hypertrophic", "GASTRITIS, HYPERTROPHIC", "Giant rugal hypertrophy", "gastritis; hypertrophic", "hypertrophic; gastritis", "Hypertrophic gastropathy", "Hyperplastic gastropathy", "Hypertrophy, giant rugal", "hypertrophic gastropathy", "hyperplastic gastropathy", "gastric mucosal hypertrophy", "Gastric mucosal hyperplasia", "Gastric mucosal hypertrophy", "Adenopapillomatosis gastrica", "giant hypertrophic gastritis", "Giant hypertrophic gastritis", "Giant Hypertrophic Gastritis", "Hypertrophic Gastritis, Giant", "gastritis; giant hypertrophic", "giant hypertrophic; gastritis", "Gastritis, Giant Hypertrophic", "Chronic hypertrophic gastritis", "Hypertrophic bulbous gastritis", "Massive hypertrophic gastritis", "giant hypertrophic gastropathy", "Menetrier's disease (diagnosis)", "Gastritis hypertrophic gigantica", "Gastritis hypertrophica gigantea", "Hypertrophic gastritis (disorder)", "Gastritis hypertrophica gigantica", "Gastroenteropathy, protein losing", "hypertrophic gastritis (diagnosis)", "Giant rugal hypertrophy of stomach", "giant rugal hypertrophy of stomach", "Hypertrophic gastropathy (disorder)", "Hypertrophic proliferative gastritis", "familial giant hypertrophic gastritis", "GASTRITIS, FAMILIAL GIANT HYPERTROPHIC", "Gastritis, Familial Giant Hypertrophic", "gastritis, familial giant hypertrophic", "giant hypertrophy of the gastric mucosa", "GASTRITIS GIANT HYPERTROPHIC MENETRIERS", "hypoproteinemic hypertrophic gastropathy", "Hypoproteinemic hypertrophic gastropathy", "GASTRITIS GIANT HYPERTROPHIC <MENETRIERS>", "Polypoid swelling of gastric mucous membrane", "Hyperplastic gastropathy of mucous cell type", "Proliferative chronic hypertrophic gastritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric mucosal hypertrophy", "shortest_name_length": 9}
{"curie": "MONDO:0031014", "names": ["Autoimmune Gastritis", "autoimmune gastritis", "autoimmune gastritis (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune gastritis", "shortest_name_length": 20}
{"curie": "UMLS:C1336548", "names": ["ALCL, systemic", "Systemic Anaplastic Large Cell Lymphoma", "Anaplastic large-cell lymphoma, primary systemic type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Systemic Anaplastic Large Cell Lymphoma", "shortest_name_length": 14}
{"curie": "MONDO:0100052", "names": ["acetazolamide-responsive hereditary episodic ataxia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acetazolamide-responsive hereditary episodic ataxia", "shortest_name_length": 51}
{"curie": "MONDO:0011090", "names": ["HCFP", "MBS2 (formerly)", "Mobius syndrome 2 (formerly)", "Moebius syndrome 2 (formerly)", "hereditary congenital facial paresis", "facial paresis hereditary congenital", "facial paresis, hereditary congenital", "Isolated hereditary congenital facial paralysis", "isolated hereditary congenital facial paralysis", "facial palsy, congenital, unilateral or bilateral", "FACIAL PALSY, CONGENITAL, UNILATERAL OR BILATERAL", "Facial Palsy, Congenital, Unilateral Or Bilateral", "Isolated hereditary congenital facial paralysis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated hereditary congenital facial paralysis", "shortest_name_length": 4}
{"curie": "UMLS:C2348101", "names": ["Destructive Arthritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Destructive Arthritis", "shortest_name_length": 21}
{"curie": "UMLS:C0017183", "names": ["Gastrointestinal Malfunction Arising from Mental Factor", "Gastrointestinal malfunction arising from mental factors"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal malfunction arising from mental factors", "shortest_name_length": 55}
{"curie": "MONDO:0010276", "names": ["radioulnar synostosis, radial RAY abnormalities, and severe malformations in the MALE", "RADIOULNAR SYNOSTOSIS, RADIAL RAY ABNORMALITIES, AND SEVERE MALFORMATIONS IN THE MALE", "Radioulnar Synostosis, Radial Ray Abnormalities, and Severe Malformations in the Male", "radioulnar synostosis, radial ray abnormalities, and severe malformations in the male"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radioulnar synostosis, radial ray abnormalities, and severe malformations in the male", "shortest_name_length": 85}
{"curie": "MONDO:0006692", "names": ["central pontine myelinosis", "Central pontine myelolysis", "Central pontine myelinosis", "Central pontine myelinolysis", "Central Pontine Myelinolysis", "central pontine myelinolysis", "Central Pontine Myelinoclasis", "Myelinolysis, Central Pontine", "Pontine Myelinolysis, Central", "MYELINOLYSIS, CENTRAL PONTINE", "MYELINOCLASIS, CENTRAL PONTINE", "myelinolysis; pontine, central", "osmotic demyelination syndrome", "Myelinoclasis, Central Pontine", "Central pontine myelinolysis (disorder)", "central pontine myelinolysis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central pontine myelinolysis", "shortest_name_length": 26}
{"curie": "MONDO:0000774", "names": ["autoimmune neuropathy", "autoimmune peripheral neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune neuropathy", "shortest_name_length": 21}
{"curie": "MONDO:0004182", "names": ["stage IVb bladder cancer", "stage IVB bladder cancer", "Stage IVB Bladder Cancer", "Jewett-Marshall bladder cancer", "stage IVB urinary bladder cancer", "Stage IVB Urinary Bladder Cancer", "Stage IVB Urinary Bladder Carcinoma", "stage IVB urinary bladder carcinoma", "Jewett-Marshall Stage D2 Bladder Cancer", "Jewett-Marshall stage D1 bladder cancer", "Jewett-Marshall stage D2 bladder cancer", "Jewett-Marshall Stage D2 Urinary Bladder Cancer", "Jewett-Marshall stage D2 urinary bladder cancer", "Jewett-Marshall stage D2 urinary bladder carcinoma", "Jewett-Marshall Stage D2 Urinary Bladder Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stage IVb bladder cancer", "shortest_name_length": 24}
{"curie": "UMLS:C5447280", "names": ["Invasive Male Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Invasive Male Breast Carcinoma", "shortest_name_length": 30}
{"curie": "UMLS:C1332537", "names": ["Salivary Gland Myoepithelioma", "Benign Salivary Gland Myoepithelioma", "benign myoepithelioma of salivary gland", "Benign Myoepithelioma of the Salivary Gland", "benign myoepithelioma of salivary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign myoepithelioma of salivary gland", "shortest_name_length": 29}
{"curie": "UMLS:C2987215", "names": ["Beta Thalassemia Plus Structural Variants"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Beta Thalassemia Plus Structural Variants", "shortest_name_length": 41}
{"curie": "MONDO:0017327", "names": ["NGCO", "Primary non-gestational ovarian choriocarcinoma", "primary non-gestational ovarian choriocarcinoma", "primary non-gestational choriocarcinoma of ovary", "Primary non-gestational choriocarcinoma of ovary", "Primary non-gestational choriocarcinoma of ovary (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary non-gestational choriocarcinoma of ovary", "shortest_name_length": 4}
{"curie": "MONDO:0100124", "names": ["NAA10-related syndrome", "NAA10 X-linked syndromic intellectual disability", "X-linked syndromic intellectual disability caused by mutation in NAA10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "NAA10-related syndrome", "shortest_name_length": 22}
{"curie": "MONDO:0019571", "names": ["ADCL", "autosomal dominant cutis laxa", "cutis laxa autosomal dominant", "Autosomal dominant cutis laxa", "Cutis Laxa, Autosomal Dominant", "Cutis laxa, autosomal dominant", "cutis laxa, autosomal dominant", "cutis laxa autosomal dominant (diagnosis)", "Cutis laxa, autosomal dominant (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant cutis laxa", "shortest_name_length": 4}
{"curie": "MONDO:0033280", "names": ["NPHS16", "nephrotic syndrome 16", "nephrotic syndrome type 16", "NEPHROTIC SYNDROME, TYPE 16", "nephrotic syndrome, type 16"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrotic syndrome 16", "shortest_name_length": 6}
{"curie": "MONDO:0022615", "names": ["burn goodship syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "burn goodship syndrome", "shortest_name_length": 22}
{"curie": "MONDO:0004644", "names": ["subacute monocytic leukemia", "Subacute monocytic leukemia", "leukemia monocytic subacute", "Subacute monocytic leukaemia", "Monocytic leukemia, subacute", "Subacute monocytoid leukemia", "Subacute myelogenous leukemia", "Monocytic leukaemia, subacute", "monocytic; leukemia, subacute", "Subacute granulocytic leukemia", "Subacute myelogenous leukaemia", "[M]Subacute monocytic leukemia", "Subacute granulocytic leukaemia", "[M]Subacute monocytic leukaemia", "Subacute monocytic leukemia (disorder)", "subacute monocytic leukemia (diagnosis)", "Subacute monocytic leukemia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subacute monocytic leukemia", "shortest_name_length": 27}
{"curie": "MONDO:0016652", "names": ["Del(2)(q31.1)", "Monosomy 2q31.1", "monosomy 2q31.1", "2q31.1 microdeletion syndrome", "2q31.1 microdeletion syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "2q31.1 microdeletion syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0032857", "names": ["IDIS", "DIAR11", "diarrhea 11, malabsorptive, congenital", "DIARRHEA 11, MALABSORPTIVE, CONGENITAL", "Intractable Diarrhea of Infancy Syndrome", "INTRACTABLE DIARRHEA OF INFANCY SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diarrhea 11, malabsorptive, congenital", "shortest_name_length": 4}
{"curie": "UMLS:C4528201", "names": ["Refractory Soft Tissue Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Soft Tissue Sarcoma", "shortest_name_length": 30}
{"curie": "MONDO:0002579", "names": ["orbit embryonal rhabdomyosarcoma", "orbit rhabdomyosarcoma embryonal", "Orbit Embryonal Rhabdomyosarcoma", "embryonal rhabdomyosarcoma of orbit", "Embryonal Rhabdomyosarcoma of Orbit", "Embryonal Rhabdomyosarcoma of the Orbit", "Embryonal Rhabdomyosarcoma of the orbit", "embryonal rhabdomyosarcoma of the orbit", "embryonal rhabdomyosarcoma of orbit (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orbit embryonal rhabdomyosarcoma", "shortest_name_length": 32}
{"curie": "MONDO:0017442", "names": ["complete phocomelia of lower limb", "Complete phocomelia of lower limb", "Congenital absence of thigh AND leg", "Congenital absence of thigh and leg", "Phocomelia, complete, of lower limb", "complete phocomelia of a lower limb", "Complete phocomelia of lower limb (disorder)", "thigh; absent, lower leg absent, foot present", "complete phocomelia of lower limb (diagnosis)", "Femorotibiofibular intercalary transverse meromelia", "congenital absence of thigh and lower leg with foot present", "Congenital absence of thigh and lower leg with foot present", "congenital deformity absence thigh and lower leg with foot present", "Congenital absence of unspecified thigh and lower leg with foot present", "congenital absence of thigh and lower leg with foot present (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital absence of thigh and lower leg with foot present", "shortest_name_length": 33}
{"curie": "MONDO:0008551", "names": ["TLPD", "BARNES SYNDROME", "Barnes syndrome", "THORACOPELVIC DYSOSTOSIS", "Thoracopelvic Dysostosis", "THORACOPELVIC dysostosis", "thoracolaryngopelvic dysplasia", "THORACOLARYNGOPELVIC dysplasia", "Thoracolaryngopelvic dysplasia", "THORACOLARYNGOPELVIC DYSPLASIA", "Thoracolaryngopelvic dysplasia syndrome", "Autosomal dominant thoracolaryngopelvic dysplasia", "autosomal dominant thoracolaryngopelvic dysplasia", "Thoracolaryngopelvic dysplasia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thoracolaryngopelvic dysplasia", "shortest_name_length": 4}
{"curie": "UMLS:C1333054", "names": ["Ciliary Body Spindle Cell Type B Melanoma", "Spindle Cell Type B Melanoma of Ciliary Body", "Spindle Cell Type B Melanoma of the Ciliary Body"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ciliary Body Spindle Cell Type B Melanoma", "shortest_name_length": 41}
{"curie": "MONDO:0020040", "names": ["Merms", "XY Female", "XY female", "xy female", "46,XY DSD", "xy females", "DSD, 46,XY", "46, XY DSD", "XY females", "females xy", "46,XY DSDs", "DSDs, 46,XY", "46, XY female", "XY females (disorder)", "karyotype; 46,XY, female", "Male pseudohermaphroditism", "Male Pseudohermaphroditism", "Pseudohermaphroditism male", "male pseudohermaphroditism", "Pseudohermaphroditism, Male", "Female with 46 XY karyotype", "pseudohermaphroditism; male", "Male Pseudohermaphroditisms", "PSEUDOHERMAPHRODITISM, MALE", "Female with 46,XY karyotype", "female with 46,XY karyotype", "Female with 46, XY karyotype", "Pseudohermaphroditisms, Male", "Male pseudohermaphroditism NOS", "46,XY disorder of sex development", "46,XY disorders of Sex development", "Disorder of Sex Development, 46,XY", "46,XY Disorders of Sex Development", "46, XY Disorders of Sex Development", "46,XY Differences of Sex Development", "46,XY differences of Sex development", "Pseudohermaphroditism syndrome, male", "Male pseudohermaphroditism (disorder)", "46, XY disorders of sexual development", "female with 46,XY karyotype (diagnosis)", "46,XY disorder of sex development (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "46,XY disorder of sex development", "shortest_name_length": 5}
{"curie": "MONDO:0000754", "names": ["ano fistula", "fistula anal", "ANAL FISTULA", "Anal Fistula", "anal fistula", "Fistula anal", "Anal fistula", "Fistula;anal", "Fistula, Anal", "anal fistulas", "anus; fistula", "fistula; anal", "ano fistula in", "fistula in ano", "Fistula in ano", "Rectal Fistula", "fistula-in-ano", "Fistula-in-ano", "in ano fistula", "fistula; in ano", "Fistula of anus", "in ano; fistula", "fistula anorectal", "Anorectal Fistula", "Anorectal fistula", "anorectal fistula", "anorectal fistulas", "fistula; anorectal", "FISTULA, ANORECTAL", "anorectal; fistula", "anal fistula (___cm)", "anal fistula (disease)", "anal fistula (diagnosis)", "fistula-in-ano (diagnosis)", "Fistula of anus (disorder)", "Anorectal fistula (disorder)", "anal fistula (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anal fistula", "shortest_name_length": 11}
{"curie": "MONDO:0015836", "names": ["Bicervical bicornuate uterus with patent cervix and vagina"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bicervical bicornuate uterus with patent cervix and vagina", "shortest_name_length": 58}
{"curie": "UMLS:C0334557", "names": ["Benign odontogenic tumor", "Benign Odontogenic Tumor", "ODONTOGENIC TUMOR, BENIGN", "Odontogenic tumor, benign", "Benign odontogenic tumour", "tumor; odontogenic, benign", "Odontogenic tumour, benign", "odontogenic; tumor, benign", "Benign Odontogenic Neoplasm", "Odontogenic tumor, benign (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Odontogenic tumor, benign", "shortest_name_length": 24}
{"curie": "MONDO:0012489", "names": ["CTRCT23", "CATARACT 23", "cataract 23", "cataract type 23", "lamellar cataract 23", "cataract 23, lamellar", "cataract 23, multiple types", "CATARACT 23, MULTIPLE TYPES", "CRYBA4 early-onset non-syndromic cataract", "CATARACT 23, MULTIPLE TYPES, WITH OR WITHOUT MICROCORNEA", "cataract 23, multiple types, with or without microcornea", "early-onset non-syndromic cataract caused by mutation in CRYBA4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 23", "shortest_name_length": 7}
{"curie": "UMLS:C0334446", "names": ["Type B Spindle Cell Melanoma", "Spindle cell melanoma, type B", "melanoma; spindle cell type B", "Spindle cell melanoma - type B", "spindle cell; melanoma, type B", "Malignant Spindle Cell Type B Melanoma", "Spindle Cell Type B Malignant Melanoma", "Spindle cell melanoma, type B (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spindle cell melanoma, type B", "shortest_name_length": 28}
{"curie": "MONDO:0025136", "names": ["bovine tuberculosis", "bovine Tuberculoses", "Bovine tuberculosis", "cattle tuberculosis", "Bovine Tuberculosis", "Bovine Tuberculoses", "Tuberculoses, bovine", "Tuberculosis, Bovine", "Tuberculoses, Bovine", "tuberculosis, bovine", "Tuberculosis in cattle", "Infection due to Mycobacterium bovis", "Infection caused by Mycobacterium bovis", "Infection caused by Mycobacterium bovis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tuberculosis, bovine", "shortest_name_length": 19}
{"curie": "MONDO:0016061", "names": ["immunodeficiency with factor H anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency with factor H anomaly", "shortest_name_length": 38}
{"curie": "MONDO:0010422", "names": ["AD16", "Alzheimer Disease 16", "ALZHEIMER DISEASE 16", "Alzheimer disease 16", "Alzheimer's disease 16", "Alzheimer's disease type 16", "Alzheimer's disease 16, late onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alzheimer disease 16", "shortest_name_length": 4}
{"curie": "MONDO:0011143", "names": ["RCD2", "CORD6", "CONE-ROD DYSTROPHY 6", "cone-rod dystrophy 6", "Cone-Rod Dystrophy 6", "Retinal cone dystrophy 2", "retinal cone dystrophy 2", "RETINAL CONE DYSTROPHY 2", "cone-rod dystrophy type 6", "GUCY2D cone-rod dystrophy", "cone-rod dystrophy caused by mutation in GUCY2D", "Cone degeneration, autosomal dominant progressive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cone-rod dystrophy 6", "shortest_name_length": 4}
{"curie": "MONDO:0022140", "names": ["CBS", "Charles Bonnet syndrome", "charles bonnet syndrome", "Charles Bonnet Syndrome", "Charles bonnet syndrome", "Charles Bonnet syndrome (disorder)", "Charles Bonnet syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charles bonnet syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C0751461", "names": ["Tetraplegic spinal paralysis", "Quadriplegic spinal paralysis", "Quadriplegic Spinal Paralysis", "Paralysis, Spinal, Quadriplegic", "Quadriplegic spinal paralysis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paralysis, Spinal, Quadriplegic", "shortest_name_length": 28}
{"curie": "UMLS:C0036305", "names": ["Schamberg", "schamberg disease", "Schamberg Disease", "Schambergs Disease", "Disease, Schamberg", "schambergs disease", "Schambergs disease", "Schamberg's purpura", "schamberg's purpura", "schamberg's disease", "Schamberg's Disease", "Schamberg's disease", "Disease, Schamberg's", "Schamberg; dermatitis", "dermatitis; Schamberg", "progressive pigmented purpura", "purpura progressive pigmented", "Progressive pigmented purpura", "Schamberg; pigmented dermatosis", "progressive; pigmented dermatosis", "pigmentary; dermatosis, Schamberg", "dermatosis; pigmentary, Schamberg", "progressive pigmentary dermatosis", "dermatosis pigmentary progressive", "Progressive pigmentary dermatosis", "pigmentary; dermatosis, progressive", "progressive; dermatosis, pigmentary", "dermatosis; pigmentary, progressive", "progressive pigmentary dermatosis (diagnosis)", "Progressive pigmentary dermatosis of Schamberg", "progressive pigmentary dermatosis (Schamberg's disease)", "Progressive pigmentary dermatosis of Schamberg (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Schamberg Disease", "shortest_name_length": 9}
{"curie": "MONDO:0012973", "names": ["IBD26", "INFLAMMATORY BOWEL DISEASE 26", "inflammatory bowel disease 26", "Inflammatory Bowel Disease 26", "inflammatory bowel disease type 26"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory bowel disease 26", "shortest_name_length": 5}
{"curie": "UMLS:C4527061", "names": ["Clinical Stage IIB Merkel Cell Carcinoma AJCC v8", "Clinical Stage IIB Neuroendocrine Carcinoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage IIB Merkel Cell Carcinoma AJCC v8", "shortest_name_length": 48}
{"curie": "UMLS:C0032749", "names": ["Post-Kala-azar dermal leishmanioid", "post-kala-azar dermal leishmaniasis", "Post Kala-Azar Dermal Leishmaniasis", "Post kala-azar dermal leishmaniasis", "Post-kala-azar dermal leishmaniasis", "PKDL - Post-Kala-azar dermal leishmanioid", "Post-kala-azar dermal leishmaniasis (disorder)", "post-kala-azar dermal leishmaniasis (diagnosis)", "Infection by leishmaniasis, dermal, post-kala-azar"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post-kala-azar dermal leishmaniasis", "shortest_name_length": 34}
{"curie": "UMLS:C4525259", "names": ["Stage I Intrahepatic Bile Duct Cancer", "Stage I Intrahepatic Bile Duct Cancer AJCC v8", "Stage I Intrahepatic Bile Duct Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Intrahepatic Bile Duct Cancer AJCC v8", "shortest_name_length": 37}
{"curie": "UMLS:C0677958", "names": ["Stage IV Non-Hodgkin Lymphoma", "Non-Hodgkin's lymphoma stage IV", "Non-Hodgkin's Lymphoma Stage IV", "Stage IV Non-Hodgkin's Lymphoma", "Non-Hodgkin's lymphoma NOS stage IV", "Ann Arbor Stage IV Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Non-Hodgkin Lymphoma", "shortest_name_length": 29}
{"curie": "MONDO:0003556", "names": ["Endometrial Adenosquamous Cancer", "ENDOMETRIAL CANCER ADENOSQUAMOUS", "endometrial adenosquamous cancer", "endometrium adenosquamous carcinoma", "endometrial adenosquamous carcinoma", "Endometrial Adenosquamous Carcinoma", "Adenosquamous carcinoma of Endometrium", "adenosquamous carcinoma of endometrium", "adenosquamous carcinoma of the endometrium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometrial adenosquamous carcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C0019049", "names": ["Hemoglobinuria due to Hemolysis from External Causes", "Hemoglobinuria due to hemolysis from external causes", "hemoglobinuria due to hemolysis from external causes", "Haemoglobinuria due to haemolysis from external causes", "Hemoglobinuria due to hemolysis from external causes (disorder)", "hemoglobinuria due to hemolysis from external causes (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemoglobinuria due to hemolysis from external causes", "shortest_name_length": 52}
{"curie": "MONDO:0003862", "names": ["Melanotic psammomatous MPNST", "melanocytic psammomatous MPNST", "Melanocytic Psammomatous MPNST", "Malignant Melanotic Psammomatous Peripheral Nerve Sheath Tumor", "Melanotic Psammomatous Malignant Peripheral Nerve Sheath Tumor", "melanotic psammomatous malignant peripheral nerve sheath tumor", "Melanocytic Psammomatous Malignant Peripheral Nerve Sheath Tumor", "melanocytic psammomatous malignant peripheral nerve sheath tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melanotic psammomatous malignant peripheral nerve sheath tumor", "shortest_name_length": 28}
{"curie": "UMLS:C0853853", "names": ["Pneumonia hemophilus", "hemophilus pneumonia", "Hemophilus pneumonia", "Haemophilus pneumonia", "Pneumonia haemophilus", "haemophilus pneumonia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pneumonia hemophilus", "shortest_name_length": 20}
{"curie": "MONDO:0011390", "names": ["FSGS2", "focal segmental glomerulosclerosis 2", "Focal Segmental Glomerulosclerosis 2", "FOCAL SEGMENTAL GLOMERULOSCLEROSIS 2", "glomerulosclerosis, focal segmental, 2", "Glomerulosclerosis, Focal Segmental, 2", "GLOMERULOSCLEROSIS, FOCAL SEGMENTAL, 2", "TRPC6 focal segmental glomerulosclerosis", "focal segmental glomerulosclerosis type 2", "focal segmental glomerulosclerosis caused by mutation in TRPC6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal segmental glomerulosclerosis 2", "shortest_name_length": 5}
{"curie": "MONDO:0017477", "names": ["lower limb hypertrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lower limb hypertrophy", "shortest_name_length": 22}
{"curie": "UMLS:C0270847", "names": ["Childhood Benign Focal Epilepsy", "Benign Focal Epilepsy, Childhood", "Benign focal epilepsy of childhood", "Benign focal epilepsy of childhood (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Focal Epilepsy, Childhood", "shortest_name_length": 31}
{"curie": "UMLS:C2984901", "names": ["Malignant Esophageal Peripheral Nerve Sheath Tumor", "Esophageal Malignant Peripheral Nerve Sheath Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Malignant Peripheral Nerve Sheath Tumor", "shortest_name_length": 50}
{"curie": "MONDO:0030044", "names": ["PTORCH3", "pseudo-torch syndrome 3", "pseudo-TORCH syndrome 3", "PSEUDO-TORCH SYNDROME 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudo-TORCH syndrome 3", "shortest_name_length": 7}
{"curie": "MONDO:0037870", "names": ["valine metabolism disease", "disorder of valine metabolism", "Disorder of valine metabolism", "valine metabolic process disease", "disorder of valine metabolic process", "Disorder of valine metabolism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "valine metabolism disease", "shortest_name_length": 25}
{"curie": "MONDO:0019640", "names": ["PUV", "posterior urethral valve", "Posterior Urethral Valve", "Posterior urethral valve", "posterior urethral valves", "Posterior urethral valves", "URETHRAL, POSTERIOR VALVES", "PUV - Posterior urethral valve", "Congenital posterior urethral valve", "congenital posterior urethral valves", "Congenital Posterior Urethral Valves", "Congenital posterior urethral valves", "Congenital posterior urethral valves (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "posterior urethral valve", "shortest_name_length": 3}
{"curie": "UMLS:C5668440", "names": ["Refractory Indolent B-Cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Indolent B-Cell Non-Hodgkin Lymphoma", "shortest_name_length": 47}
{"curie": "MONDO:0000766", "names": ["endothelial dystrophy", "Endothelial corneal dystrophy", "corneal endothelial dystrophy", "Corneal endothelial dystrophy", "endothelial corneal dystrophy", "endothelial dystrophy of cornea", "Dystrophy of corneal endothelium", "Posterior membrane corneal dystrophy", "Descemet's membrane corneal dystrophy", "Corneal endothelial dystrophy (disorder)", "endothelial corneal dystrophy (diagnosis)", "corneal dystrophy (disease) of corneal epithelium", "endothelial dystrophy of cornea (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal endothelial dystrophy", "shortest_name_length": 21}
{"curie": "UMLS:C1332601", "names": ["Borderline Primary Cutaneous CD30+ T-Cell Lymphoproliferative Disorder", "Borderline Primary Cutaneous CD30-Positive T-Cell Lymphoproliferative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Primary Cutaneous CD30-Positive T-Cell Lymphoproliferative Disorder", "shortest_name_length": 70}
{"curie": "MONDO:0008481", "names": ["OA neck", "Neck Arthritis", "Neck arthritis", "neck arthritis", "neck spondylosis", "Arthritis of neck", "arthritis of neck", "cervical arthritis", "Cervical arthritis", "neck osteoarthritis", "Cervical spondylitis", "cervical spondylosis", "Spondylosis;cervical", "Cervical Spondylosis", "Cervical spondylosis", "CERVICAL SPONDYLITIS", "cervical; spondylosis", "spondylosis, cervical", "spondylosis; cervical", "SPONDYLOSIS, CERVICAL", "Spondylosis, Cervical", "Osteoarthritis of neck", "Cervical osteoarthritis", "Cervical Osteoarthritis", "cervical osteoarthritis", "Cervical spondylarthritis", "CS - Cervical spondylosis", "CERVICAL SPINE SPONDYLOSIS", "cervical spine degeneration", "Cervical spine degeneration", "Osteoarthritis;spine;cervical", "Cervical arthritis (disorder)", "Cervical spondylosis (disorder)", "Osteoarthritis of cervical spine", "cervical spondylosis (diagnosis)", "osteoarthritis vertebral cervical", "Cervical or cervicodorsal arthritis", "Cervical osteoarthritis (diagnosis)", "osteoarthritis of the cervical spine", "Cervical or cervicodorsal osteoarthritis", "Cervical or cervicodorsal spondylarthritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondylosis, cervical", "shortest_name_length": 7}
{"curie": "MONDO:0007974", "names": ["MRD1", "CHROMOSOME 2q23.1 DELETION SYNDROME", "chromosome 2Q23.1 deletion syndrome", "CHROMOSOME 2q23.1 DUPLICATION SYNDROME", "autosomal dominant mental retardation 1", "Mental Retardation, Autosomal Dominant 1", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 1", "mental retardation, autosomal dominant 1", "autosomal dominant intellectual disability 1", "mental retardation, autosomal dominant type 1", "intellectual disability, autosomal dominant 1", "intellectual disability, autosomal dominant type 1", "autosomal dominant intellectual developmental disorder 1", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 1", "autosomal dominant non-syndromic intellectual disability 1", "MBD5 autosomal dominant non-syndromic intellectual disability", "autosomal dominant non-syndromic intellectual disability caused by mutation in MBD5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 1", "shortest_name_length": 4}
{"curie": "MONDO:0014594", "names": ["DFNA67", "autosomal dominant deafness 67", "deafness, autosomal dominant 67", "DEAFNESS, AUTOSOMAL DOMINANT 67", "deafness, autosomal dominant type 67", "autosomal dominant nonsyndromic deafness 67", "autosomal dominant nonsyndromic hearing loss 67", "OSBPL2 autosomal dominant nonsyndromic deafness", "autosomal dominant nonsyndromic deafness type 67", "autosomal dominant nonsyndromic deafness caused by mutation in OSBPL2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 67", "shortest_name_length": 6}
{"curie": "MONDO:0021879", "names": ["Anaplastic small cell lymphoma", "anaplastic small cell lymphoma", "Small Cell Variant Anaplastic Large Cell Lymphoma", "small cell variant anaplastic large cell lymphoma", "Small cell variant of anaplastic large cell lymphoma", "small cell variant of anaplastic large cell lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small cell variant anaplastic large cell lymphoma", "shortest_name_length": 30}
{"curie": "MONDO:0007772", "names": ["PHA2A", "Pseudohypoaldosteronism type 2A", "pseudohypoaldosteronism type 2A", "PSEUDOHYPOALDOSTERONISM, TYPE IIA", "Pseudohypoaldosteronism, Type IIa", "pseudohypoaldosteronism, type IIA", "Familial Hypertensive Hyperkalemia", "Hyperkalemia, Familial Hypertensive", "Hypertensive Hyperkalemia, Familial", "hypertensive hyperkalemia, familial", "HYPERTENSIVE HYPERKALEMIA, FAMILIAL", "Familial Hypertensive Hyperkalemias", "Hypertensive Hyperkalemias, Familial", "Hyperkalemias, Familial Hypertensive", "Familial Hyperpotassemia and Hypertension", "Gordon hyperkalemia-hypertension syndrome", "HYPERPOTASSEMIA AND HYPERTENSION, FAMILIAL", "hyperpotassemia and hypertension, familial", "Pseudohypoaldosteronism type 2A (disorder)", "Hyperpotassemia and Hypertension, Familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudohypoaldosteronism type 2A", "shortest_name_length": 5}
{"curie": "MONDO:0008874", "names": ["BANGSTAD SYNDROME", "Bangstad syndrome", "Ataxia-diabetes-goiter-gonadal insufficiency syndrome", "ataxia-diabetes-goiter-gonadal insufficiency syndrome", "Bird-headed dwarfism with progressive ataxia, insulin-resistant diabetes, goiter and primary gonadal insufficiency", "Bird-headed dwarfism with progressive ataxia, insulin-resistant diabetes, goiter, and primary gonadal insufficiency", "Bird-headed dwarfism with progressive ataxia, insulin-resistant diabetes, goitre, and primary gonadal insufficiency", "BIRD-HEADED DWARFISM WITH PROGRESSIVE ATAXIA, INSULIN-RESISTANT DIABETES, GOITER, AND PRIMARY GONADAL INSUFFICIENCY", "Bird-headed dwarfism with progressive ataxia, insulin-resistant diabetes, goiter, and primary gonadal insufficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bangstad syndrome", "shortest_name_length": 17}
{"curie": "UMLS:C4054188", "names": ["Ph-Like", "Ph-like ALL", "Ph-Like ALL", "BCR-ABL1-like ALL", "Philadelphia-like ALL", "Ph-Like Acute Lymphoblastic Leukemia", "BCR-ABL1-like Acute Lymphoblastic Leukemia", "Philadelphia-Like Acute Lymphoblastic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ph-Like Acute Lymphoblastic Leukemia", "shortest_name_length": 7}
{"curie": "MONDO:0007148", "names": ["appendicitis, proneness to", "APPENDICITIS, PRONENESS TO", "appendicitis, susceptibility"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "appendicitis, proneness to", "shortest_name_length": 26}
{"curie": "UMLS:C4745251", "names": ["Grade 1 Ovarian Teratoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade 1 Ovarian Teratoma", "shortest_name_length": 24}
{"curie": "MONDO:0009550", "names": ["HOMG3", "Hypomagnesemia primary", "renal hypomagnesemia 3", "hypomagnesemia 3, renal", "Renal hypomagnesemia type 3", "renal hypomagnesemia type 3", "Renal hypomagnesaemia type 3", "CLDN16 primary hypomagnesemia", "isolated renal hypomagnesemia", "hypomagnesemia, isolated renal", "CLDN16 familial primary hypomagnesemia", "FHHNC without severe ocular involvement", "hypercalciuria, childhood, self-limiting", "HYPERCALCIURIA, CHILDHOOD, SELF-LIMITING", "magnesium, defect in renal tubular transport of", "primary hypomagnesemia caused by mutation in CLDN16", "familial primary hypomagnesemia caused by mutation in CLDN16", "hypomagnesemia, familial, with hypercalciuria and nephrocalcinosis", "primary hypomagnesemia due to defect in renal tubular transport of magnesium", "hypomagnesemia, primary, due to defect in renal tubular Transport of magnesium", "hypomagnesemia, primary, due to defect in renal tubular Transport Of magnesium", "primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement", "Primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement", "Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement", "familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement", "Familial primary hypomagnesaemia with hypercalciuria and nephrocalcinosis without severe ocular involvement", "primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement (diagnosis)", "hypomagnesemia, familial, with hypercalciuria and nephrocalcinosis hypercalciuria, childhood, self-limiting, included", "Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal hypomagnesemia 3", "shortest_name_length": 5}
{"curie": "MONDO:0015238", "names": ["Bosma Henkin Christiansen syndrome", "Bosma arhinia microphthalmia syndrome", "arhinia choanal atresia microphthalmia", "arrhinia-choanal atresia-microphthalmia syndrome", "congenital absence of nose and anterior nasopharynx"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arrhinia-choanal atresia-microphthalmia syndrome", "shortest_name_length": 34}
{"curie": "UMLS:C4553791", "names": ["0is", "stage 0is bladder cancer", "Stage 0is Bladder Cancer", "Stage 0is Bladder Cancer AJCC v8", "stage 0is bladder cancer AJCC v8", "Stage 0is Bladder Carcinoma AJCC v8", "stage 0is bladder carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0is Bladder Cancer AJCC v8", "shortest_name_length": 3}
{"curie": "MONDO:0016780", "names": ["paternal del(14)(q32.2)", "paternal monosomy 14q32.2", "paternal 14q32.2 microdeletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paternal 14q32.2 microdeletion syndrome", "shortest_name_length": 23}
{"curie": "UMLS:C1691221", "names": ["Lower respiratory tract infection fungal", "Fungal lower respiratory tract infections"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lower respiratory tract infection fungal", "shortest_name_length": 40}
{"curie": "MONDO:0100071", "names": ["cardiocutaneous syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiocutaneous syndrome", "shortest_name_length": 24}
{"curie": "UMLS:C5206867", "names": ["Resectable Cutaneous Squamous Cell Carcinoma of the Head and Neck"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Cutaneous Squamous Cell Carcinoma of the Head and Neck", "shortest_name_length": 65}
{"curie": "UMLS:C2046665", "names": ["Salivary Gland Hodgkin Lymphoma", "Hodgkin's lymphoma of salivary gland", "Primary Salivary Gland Hodgkin Lymphoma", "Hodgkin's lymphoma of salivary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's lymphoma of salivary gland", "shortest_name_length": 31}
{"curie": "MONDO:0037737", "names": ["Peritoneal SFT", "peritoneal solitary fibrous tumor", "Peritoneal Solitary Fibrous Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peritoneal solitary fibrous tumor", "shortest_name_length": 14}
{"curie": "MONDO:0014733", "names": ["CMT4K", "SURF1-related CMT4", "Charcot-Marie-Tooth disease type 4K", "CHARCOT-MARIE-TOOTH DISEASE, TYPE 4K", "Charcot-Marie-Tooth disease, type 4K", "Charcot-Marie-Tooth disease, type 4k", "SURF1 Charcot-Marie-Tooth disease type 4", "SURF1-related Charcot-Marie-Tooth disease type 4", "SURF1-related severe demyelinating Charcot-Marie-Tooth disease", "Charcot-Marie-Tooth disease type 4 caused by mutation in SURF1", "autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4K", "CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, AUTOSOMAL RECESSIVE, TYPE 4K", "autosomal recessive demyelinating Charcot-Marie-Tooth neuropathy type 4K", "Charcot-Marie-Tooth disease, demyelinating, autosomal recessive, type 4K", "Charcot-Marie-Tooth neuropathy, demyelinating, autosomal recessive, type 4K", "CHARCOT-MARIE-TOOTH NEUROPATHY, DEMYELINATING, AUTOSOMAL RECESSIVE, TYPE 4K", "SURF1, cytochrome c oxidase assembly factor related Charcot-Marie-Tooth disease type 4", "SURF1, cytochrome c oxidase assembly factor related Charcot-Marie-Tooth disease type 4 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 4K", "shortest_name_length": 5}
{"curie": "MONDO:0015027", "names": ["FIHP", "FIHPT", "familial isolated hyperparathyroidism", "Familial Isolated Hyperparathyroidism", "Familial isolated hyperparathyroidism", "FIHPT - familial isolated hyperparathyroidism", "Hyperparathyroidism, Familial Isolated Primary", "HYPERPARATHYROIDISM, FAMILIAL ISOLATED PRIMARY", "Familial isolated hyperparathyroidism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial isolated hyperparathyroidism", "shortest_name_length": 4}
{"curie": "UMLS:C4049192", "names": ["Chest wall hematoma", "Chest wall haematoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chest wall hematoma", "shortest_name_length": 19}
{"curie": "MONDO:0025270", "names": ["animal toxoplasmosis", "Animal Toxoplasmosis", "Animal Toxoplasmoses", "animal Toxoplasmoses", "Toxoplasmoses, Animal", "Toxoplasmoses, animal", "Toxoplasmosis, Animal", "Toxoplasmosis in animals", "toxoplasmosis, non-human animal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "toxoplasmosis, non-human animal", "shortest_name_length": 20}
{"curie": "MONDO:0002953", "names": ["Infiltrating Basal Cell Carcinoma", "Infiltrating basal cell carcinoma", "infiltrative basal cell carcinoma", "infiltrating basal cell carcinoma", "Skin Infiltrating Basal Cell Carcinoma", "skin infiltrative basal cell carcinoma", "Infiltrating basal cell carcinoma, NOS", "skin infiltrating basal cell carcinoma", "Basal cell carcinoma, desmoplastic type", "Infiltrating basal cell carcinoma, sclerosing", "Infiltrating basal cell carcinoma, non-sclerosing", "Infiltrating basal cell carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin infiltrative basal cell carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0010105", "names": ["Pineal Teratoma", "teratoma, pineal", "TERATOMA, PINEAL", "Teratoma, Pineal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "teratoma, pineal", "shortest_name_length": 15}
{"curie": "UMLS:C2204430", "names": ["Tongue Sarcoma", "sarcoma of tongue", "sarcoma of tongue (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sarcoma of tongue", "shortest_name_length": 14}
{"curie": "UMLS:C1335010", "names": ["Non-Neoplastic Eyelid Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Eyelid Disorder", "shortest_name_length": 30}
{"curie": "MONDO:0023573", "names": ["Kozlowski Warren Fisher syndrome", "Cloverleaf skull generalised bone dysplasia", "cloverleaf skull generalised bone dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kozlowski Warren Fisher syndrome", "shortest_name_length": 32}
{"curie": "MONDO:0003626", "names": ["uterine ligament serous adenocarcinoma", "Uterine Ligament Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine ligament serous adenocarcinoma", "shortest_name_length": 38}
{"curie": "MONDO:0014580", "names": ["MRD33", "autosomal dominant mental retardation 33", "mental retardation, autosomal dominant 33", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 33", "autosomal dominant intellectual disability 33", "intellectual disability, autosomal dominant 33", "mental retardation, autosomal dominant type 33", "intellectual disability, autosomal dominant type 33", "autosomal dominant intellectual developmental disorder 33", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 33", "autosomal dominant non-syndromic intellectual disability 33", "DPP6 autosomal dominant non-syndromic intellectual disability", "autosomal dominant non-syndromic intellectual disability caused by mutation in DPP6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 33", "shortest_name_length": 5}
{"curie": "UMLS:C4524961", "names": ["stage 0 small intestine cancer", "Stage 0 Small Intestinal Adenocarcinoma", "Stage 0 Small Intestinal Adenocarcinoma AJCC v8", "stage 0 small intestinal adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Small Intestinal Adenocarcinoma AJCC v8", "shortest_name_length": 30}
{"curie": "MONDO:0017887", "names": ["renal cell carcinoma after neuroblastoma", "Renal Cell Cancer Associated with Neuroblastoma", "renal cell cancer associated with neuroblastoma", "Renal Cell Carcinoma Associated with Neuroblastoma", "renal cell carcinoma associated with neuroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal cell carcinoma associated with neuroblastoma", "shortest_name_length": 40}
{"curie": "MONDO:0011888", "names": ["IPD1", "IRAK4D", "IRAK4 deficiency", "IRAK-4 deficiency", "immunodeficiency 67", "invasive pneumococcal disease, protection against", "Interleukin receptor-associated kinase deficiency", "invasive pneumococcal disease, recurrent isolated, 1", "invasive pneumococcal disease, recurrent isolated, type 1", "immunodeficiency due to interleukin-1 receptor-associated kinase-4 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 67", "shortest_name_length": 4}
{"curie": "MONDO:0014890", "names": ["CISS3", "PERCHING", "CISS3, FORMERLY", "PERCHING syndrome", "PERCHING SYNDROME", "cold-induced sweating syndrome 3", "KLHL7 cold-induced sweating syndrome", "cold-induced sweating syndrome type 3", "CRISPONI/cold-induced sweating syndrome 3", "Crisponi/cold-induced sweating syndrome 3", "CRISPONI/COLD-INDUCED SWEATING SYNDROME 3, FORMERLY", "cold-induced sweating syndrome caused by mutation in KLHL7", "KLHL7-related Bohring-Opitz-like/Cold-induced sweating-like overlap syndrome", "KLHL7-related bohring-opitz-like/cold-induced sweating-like overlap syndrome", "Postural and Palatal abnormalities; Exophthalmos and Enteral-tube dependency/feeding issues; Respiratory distress and Retinitis pigmentosa; Contractures and Camptodactyly; Hypertelorism and Hirsutism; Intrauterine growth retardation (IUGR)/growth failure and Intellectual disability/developmental delay; Nevus flammeus and Neurologic malformations;and facial Gestalt/grimacing and Genitourinary abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PERCHING syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0015294", "names": ["NFD", "NSF", "Nephrogenic Systemic Fibroses", "nephrogenic systemic fibrosis", "Nephrogenic systemic fibrosis", "Nephrogenic Systemic Fibrosis", "Fibrosis, Nephrogenic Systemic", "Systemic Fibrosis, Nephrogenic", "Systemic Fibroses, Nephrogenic", "Fibroses, Nephrogenic Systemic", "nephrogenic fibrosing dermopathy", "Nephrogenic Fibrosing Dermopathy", "Nephrogenic fibrosing dermopathy", "Dermopathy, Nephrogenic Fibrosing", "Fibrosing Dermopathy, Nephrogenic", "Nephrogenic Fibrosing Dermopathies", "Dermopathies, Nephrogenic Fibrosing", "Fibrosing Dermopathies, Nephrogenic", "NSF - Nephrogenic fibrosing dermopathy", "Nephrogenic systemic fibrosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrogenic systemic fibrosis", "shortest_name_length": 3}
{"curie": "MONDO:0019255", "names": ["sphingolipidosis", "Sphingolipidosis", "Sphingolipidoses", "sphingolipidoses", "Sphingolipidosis, NOS", "Sphingolipidosis (disorder)", "Sphingolipid Storage Disease", "sphingolipidosis (diagnosis)", "Storage Disease, Sphingolipid", "Sphingolipid Storage Diseases", "Sphingolipidosis, unspecified", "Storage Diseases, Sphingolipid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sphingolipidosis", "shortest_name_length": 16}
{"curie": "MONDO:0002373", "names": ["benign mesothelioma", "mesothelioma, benign", "benign tumor of mesothelium", "benign tumor of Mesothelium", "benign tumor of mesothelial tissue", "Benign tumor of mesothelial tissue", "benign neoplasm mesothelial tissue", "Benign tumour of mesothelial tissue", "benign neoplasm of mesothelial tissue", "Benign neoplasm of mesothelial tissue", "Benign tumor of mesothelial tissue (disorder)", "benign neoplasm of mesothelial tissue (diagnosis)", "Benign neoplasm of mesothelial tissue, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign mesothelioma", "shortest_name_length": 19}
{"curie": "MONDO:0017464", "names": ["congenital pseudarthrosis of the fibula", "congenital pseudoarthrosis of the fibula"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital pseudoarthrosis of the fibula", "shortest_name_length": 39}
{"curie": "UMLS:C0015929", "names": ["fetal disease", "Fetal Disease", "disease fetal", "Fetal disease", "Foetal disease", "FETAL DISORDER", "Fetal disorder", "Fetal Disorder", "Disease, Fetal", "fetal disorder", "DISORDER FETAL", "Fetal Diseases", "Disorder fetal", "fetal diseases", "fetus disorder", "Foetal disorder", "Fetal Disorders", "fetal disorders", "Diseases, Fetal", "fetus; disorder", "disorders fetal", "disorders fetus", "FETAL DISORDERS", "FOETAL DISORDERS", "foetal disorders", "Disorder of Fetus", "Disorder fetal NOS", "Fetal disease, NOS", "Fetal disorder NOS", "Foetal disease, NOS", "Disorder foetal NOS", "Foetal disorder NOS", "Fetal disorder, NOS", "Foetal disorder, NOS", "embryo/fetus disorder", "Fetal disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fetal Diseases", "shortest_name_length": 13}
{"curie": "UMLS:C0011974", "names": ["Jacquet", "nappy rash", "Rash;nappy", "Nappy Rash", "Nappy rash", "diaper rash", "Diaper Rash", "Diaper rash", "DIAPER RASH", "Rash, Diaper", "rash; napkin", "napkin; rash", "diaper rashes", "Diaper Rashes", "Nappy rash NOS", "eczema; napkin", "napkin; eczema", "Rashes, Diaper", "Diaper erythema", "napkin; eruption", "erythema; diaper", "eruption; napkin", "diaper; erythema", "napkin dermatitis", "Dermatitis;napkin", "Diaper Dermatitis", "diaper dermatitis", "Dermatitis diaper", "Diaper dermatitis", "Jacquet's erythema", "Ammonia dermatitis", "napkin; dermatitis", "Jacquet; dermatitis", "dermatitis; Jacquet", "Jacquet's dermatitis", "Diaper or napkin rash", "Nappy rash - irritant", "Diaper rash (disorder)", "diaper rash (diagnosis)", "Diaper or napkin erythema", "Irritant napkin dermatitis", "Diaper [napkin] dermatitis", "Diaper or napkin dermatitis", "erythema in the diaper area", "Ammoniacal napkin dermatitis", "Urine-induced contact dermatitis", "Contact dermatitis caused by urine", "contact dermatitis caused by urine", "Contact dermatitis caused by urine (disorder)", "erythema in the diaper area (physical finding)", "contact dermatitis caused by urine (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diaper Rash", "shortest_name_length": 7}
{"curie": "UMLS:C5419770", "names": ["Esophageal Neuroendocrine Tumor G3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Neuroendocrine Tumor G3", "shortest_name_length": 34}
{"curie": "MONDO:0012617", "names": ["MRT9", "MRT26", "Mental Retardation, Autosomal Recessive 9", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 9", "mental retardation, autosomal recessive 9", "mental retardation, autosomal recessive 26", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 26", "mental retardation, autosomal recessive, 9/26", "intellectual disability, autosomal recessive 9", "intellectual disability, autosomal recessive 26", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 9", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 26", "autosomal recessive intellectual developmental disorder 9/26"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 9", "shortest_name_length": 4}
{"curie": "EFO:1002011", "names": ["adult onset asthma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult onset asthma", "shortest_name_length": 18}
{"curie": "MONDO:0005052", "names": ["IBD", "IBS", "colon spasm", "Colon spasm", "colon; spasm", "spasm; colon", "colon spasms", "spastic colon", "colon spastic", "Spastic colon", "mucus colitis", "Colon spastic", "SPASTIC COLON", "COLON SPASTIC", "Colitis mucous", "Mucous Colitis", "mucous colitis", "COLON, SPASTIC", "colon; spastic", "COLITIS MUCOUS", "Mucous colitis", "colons spastic", "spastic; colon", "Colitis;mucous", "Irritable colon", "Psychogenic IBS", "Spastic colitis", "nervous colitis", "Nervous colitis", "Irritable;colon", "irritable colon", "BOWEL IRRITABLE", "colon irritable", "Irritable bowel", "irritable bowel", "spastic colitis", "psychogenic IBS", "Irritable Colon", "IRRITABLE COLON", "Colitis, Mucous", "COLITIS, MUCOUS", "Colon, Irritable", "colitis; spastic", "Adaptive colitis", "Mucous Colitides", "spastic; colitis", "bowels irritable", "colon; irritable", "bowel; irritable", "Colitides, Mucous", "membranous colitis", "Membranous colitis", "Membranous Colitis", "IC - Irritable colon", "disease irritable bowel", "irritable bowel disease", "bowel disease irritable", "Irritable bowel syndrome", "IRRITABLE BOWEL SYNDROME", "Irritable Bowel Syndrome", "bowel syndrome irritable", "syndrome irritable bowel", "irritable bowel syndrome", "functional bowel disease", "BOWEL IRRITABLE SYNDROME", "Irritable colon syndrome", "Irritable Colon Syndrome", "IRRITABLE COLON SYNDROME", "Functional bowel disease", "irritable colon syndrome", "irritable bowel; syndrome", "Irritable Bowel Syndromes", "Syndrome, Irritable Bowel", "Functional bowel syndrome", "functional bowel syndrome", "irritable bowel syndromes", "bowels irritable syndrome", "syndrome; irritable bowel", "bowel; functional syndrome", "bowel; disease, functional", "Syndromes, Irritable Bowel", "syndrome; bowel, functional", "bowel; syndrome, functional", "syndrome; functional, bowel", "bowel ibs irritable syndrome", "Irritable bowel syndrome NOS", "irritable bowel disease (IBD)", "IBS - Irritable bowel syndrome", "irritable bowel syndrome (IBS)", "IBS (irritable bowel syndrome)", "Irritable bowel syndrome (disorder)", "irritable bowel syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "irritable bowel syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C1520095", "names": ["Vulvar Soft Tissue Tumor", "Vulvar Soft Tissue Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Soft Tissue Neoplasm", "shortest_name_length": 24}
{"curie": "MONDO:0013097", "names": ["GLM8", "GLIOMA SUSCEPTIBILITY 8", "glioma susceptibility 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glioma susceptibility 8", "shortest_name_length": 4}
{"curie": "MONDO:0004974", "names": ["PCC", "chromaffinoma", "Chromaffinoma", "Pheochromocytoma", "chromaffin tumor", "Chromaffin tumor", "pheochromocytoma", "phaeochromocytoma", "Phaeochromocytoma", "pheochromocytomas", "Chromaffin tumour", "Pheochromocytoma NOS", "Phaeochromocytoma NOS", "[M]Pheochromocytoma NOS", "PARAGANGLIOMA, MEDULLARY", "CHROMAFFINOMA, MEDULLARY", "Adrenal pheochromocytoma", "Adrenal Pheochromocytoma", "adrenal pheochromocytoma", "Chromaffin paraganglioma", "[M]Phaeochromocytoma NOS", "Chromaffin cell neoplasm", "Pheochromocytoma, adrenal", "pheochromocytoma syndrome", "pheochromocytoma (adrenal)", "Intraadrenal Paraganglioma", "Pheochromocytomas, adrenal", "Intraadrenal paraganglioma", "Pheochromocytoma (adrenal)", "Adrenal Gland Chromaffinoma", "adrenal gland paraganglioma", "adrenal gland Chromaffinoma", "Adrenal Gland Paraganglioma", "Pheochromocytoma (disorder)", "pheochromocytoma (diagnosis)", "Adrenal Gland Pheochromocytoma", "adrenal gland pheochromocytoma", "Adrenal medullary paraganglioma", "Adrenal Medullary Paraganglioma", "adrenal medullary paraganglioma", "Adrenal Medullary Pheochromocytoma", "adrenal medullary pheochromocytoma", "Adrenal Gland Chromaffin Paraganglioma", "adrenal gland chromaffin paraganglioma", "Pheochromocytoma (morphologic abnormality)", "chromaffin paraganglioma of the adrenal gland", "Chromaffin Paraganglioma of the Adrenal Gland", "adrenal neoplasm of uncertain behavior pheochromocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adrenal gland pheochromocytoma", "shortest_name_length": 3}
{"curie": "UMLS:C0241435", "names": ["TONGUE LEUKOPLAKIA", "Leukoplakia tongue", "tongue; leukoplakia", "leukoplakia; tongue", "Leukoplakia (tongue)", "Leukoplakia of Tongue", "Leukoplakia of tongue", "Leukoplakia lingualis", "Leucoplakia of tongue", "oral leukoplakia of tongue", "Leukoplakia of tongue (disorder)", "oral leukoplakia of tongue (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leukoplakia of tongue", "shortest_name_length": 18}
{"curie": "UMLS:C0334516", "names": ["Atypical Seminoma", "Anaplastic seminoma", "Anaplastic Seminoma", "Seminoma, anaplastic", "Seminoma, anaplastic type", "Seminoma with high mitotic index", "Testicular Seminoma with High Mitotic Index", "Seminoma, anaplastic (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Seminoma, anaplastic", "shortest_name_length": 17}
{"curie": "NCIT:C34912", "names": ["Perceptual Distortion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perceptual Distortion", "shortest_name_length": 21}
{"curie": "UMLS:C1708957", "names": ["Mediastinal Paraganglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mediastinal Paraganglioma", "shortest_name_length": 25}
{"curie": "MONDO:0007232", "names": ["BCYM3", "Brachyrachia", "brachyrachia", "BRACHYRACHIA", "Brachyolmia Type 3", "Brachyolmia type 3", "brachyolmia type 3", "BRACHYOLMIA TYPE 3", "brachyolmia autosomal dominant", "autosomal dominant brachyolmia", "Autosomal dominant brachyolmia", "BRACHYOLMIA, AUTOSOMAL DOMINANT", "brachyolmia, autosomal dominant", "Brachyolmia, Autosomal Dominant", "Brachyrachia (short spine dysplasia)", "Autosomal dominant brachyolmia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant brachyolmia", "shortest_name_length": 5}
{"curie": "MONDO:0012773", "names": ["HUNTER-MACDONALD SYNDROME", "Hunter-Macdonald Syndrome", "Hunter-Macdonald syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hunter-Macdonald syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0014853", "names": ["DFNA70", "autosomal dominant deafness 70", "deafness, autosomal dominant 70", "DEAFNESS, AUTOSOMAL DOMINANT 70", "deafness, autosomal dominant type 70", "autosomal dominant nonsyndromic deafness 70", "MCM2 autosomal dominant nonsyndromic deafness", "autosomal dominant nonsyndromic hearing loss 70", "autosomal dominant nonsyndromic deafness type 70", "autosomal dominant nonsyndromic deafness caused by mutation in MCM2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 70", "shortest_name_length": 6}
{"curie": "UMLS:C0685628", "names": ["Lumbar Rib", "LUMBAR RIB", "lumbar rib", "Lumbar rib", "lumbar ribs", "Costa lumbalis", "Thoracolumbar rib", "Full supernumerary rib", "Full supernumerary rib (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Full supernumerary rib", "shortest_name_length": 10}
{"curie": "MONDO:0020634", "names": ["Grade 3 Meningioma", "grade 3 meningioma", "Grade III Meningioma", "grade III meningioma", "meningioma, malignant", "MENINGIOMA, MALIGNANT", "WHO Grade 3 Meningioma", "Who Grade III Meningioma", "WHO Grade III Meningioma", "WHO grade III meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "grade III meningioma", "shortest_name_length": 18}
{"curie": "UMLS:C0161398", "names": ["n.opticus; injury", "optic nerve injury", "Optic nerve damage", "optic nerve trauma", "Optic Nerve Trauma", "Optic Nerve Injury", "Optic nerve injury", "Optic Nerve Damage", "Injury;nerve;optic", "Injury, Optic Nerve", "Optic Nerve Traumas", "Nerve Trauma, Optic", "injury; optic nerve", "Trauma, Optic Nerve", "Nerve Injury, Optic", "optic nerve injuries", "Traumas, Optic Nerve", "Nerve Traumas, Optic", "Optical Nerve Damage", "Optic Nerve Injuries", "Nerve Injuries, Optic", "Trauma to optic nerve", "Injuries, Optic Nerve", "Injury of optic nerve", "Optic nerve injury NOS", "Optic nerve injury, NOS", "Optic nerve (2nd) injury", "Cranial Nerve II Injuries", "Injury of optic nerve NOS", "neuropathy optic traumatic", "traumatic optic neuropathy", "Traumatic Optic Neuropathy", "Traumatic optic neuropathy", "Second Cranial Nerve Trauma", "Second cranial nerve injury", "Neuropathy, Traumatic Optic", "Optic Neuropathy, Traumatic", "traumatic optic nerve injury", "Traumatic optic nerve injury", "Trauma, Second Cranial Nerve", "Traumatic Optic Neuropathies", "Second Cranial Nerve Injuries", "Optic Neuropathies, Traumatic", "Neuropathies, Traumatic Optic", "Injury of second cranial nerve", "optic nerve injury (diagnosis)", "Second cranial nerve injury, NOS", "Traumatic optic neuropathy (diagnosis)", "Traumatic optic nerve injury (disorder)", "traumatic optic nerve injury (diagnosis)", "cranial nerve injury optic nerve traumatic neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Optic Nerve Injuries", "shortest_name_length": 17}
{"curie": "MONDO:0020552", "names": ["PSTT", "PSST", "placental site GTT", "placental-site GTT", "Placental-Site GTT", "GTT, placental-site", "GTT, placental site", "Placental Trophoblastic Tumor", "Trophoblastic Tumor, Placental", "Placental Trophoblastic Tumors", "Tumor, Placental Trophoblastic", "Tumors, Placental Trophoblastic", "Trophoblastic Tumors, Placental", "placental site trophoblastic tumor", "Placental site trophoblastic tumor", "Placental Site Trophoblastic Tumor", "Placental-Site Trophoblastic Tumor", "placental site trophoblastic tumour", "Tumor, Placental-Site Trophoblastic", "tumor; placental site trophoblastic", "Trophoblastic Tumor, Placental-Site", "Placental site trophoblastic tumour", "Placental-Site Trophoblastic Tumors", "Trophoblastic Tumor, Placental Site", "Trophoblastic Tumors, Placental-Site", "Tumors, Placental-Site Trophoblastic", "Placental site trophoblastic tumor (disorder)", "Placental Site Gestational Trophoblastic Tumor", "placental site gestational trophoblastic tumor", "Placental-Site Gestational Trophoblastic Tumor", "placental-site gestational trophoblastic tumor", "gestational trophoblastic tumor, placental site", "gestational trophoblastic tumor, placental-site", "placental-site gestational trophoblastic neoplasm", "Placental-Site Gestational Trophoblastic neoplasm", "Placental-Site Gestational Trophoblastic Neoplasm", "placental site trophoblastic tumor (morphologic abnormality)", "Placental site trophoblastic tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "placental site trophoblastic tumor", "shortest_name_length": 4}
{"curie": "MONDO:0010305", "names": ["CCDS1", "SLC6A8 deficiency", "Slc6a8 Deficiency", "Creatine Transporter Defect", "creatine transporter defect", "CREATINE TRANSPORTER DEFECT", "X-Linked Creatine Deficiency", "X-linked creatine deficiency", "creatine deficiency, X-linked", "Creatine deficiency, X-linked", "Creatine Transporter Deficiency", "creatine transporter deficiency", "Creatine transporter deficiency", "X-linked creatine deficiency syndrome", "Creatine Deficiency Syndrome, X-Linked", "CREATINE DEFICIENCY SYNDROME, X-LINKED", "creatine deficiency syndrome, X-linked", "X-linked creatine deficiency (disorder)", "Cerebral creatine deficiency syndrome 1", "Cerebral Creatine Deficiency Syndrome 1", "CEREBRAL CREATINE DEFICIENCY SYNDROME 1", "cerebral creatine deficiency syndrome 1", "X-linked creatine transporter deficiency", "X-Linked Creatine Transporter Deficiency", "cerebral creatine deficiency syndrome type 1", "Slc6a8-Related Creatine Transporter Deficiency", "SLC6A8 related creatine transporter deficiency", "cerebral creatine deficiency syndrome 1, X-linked recessive", "Mental retardation, X-linked, with creatine transport deficiency", "mental retardation, X-linked, with creatine Transport deficiency", "MENTAL RETARDATION, X-LINKED, WITH CREATINE TRANSPORT DEFICIENCY", "mental retardation, X-linked, with creatine transport deficiency", "intellectual disability, X-linked, with creatine Transport deficiency", "intellectual disability, X-linked, with creatine transport deficiency", "mental retardation, X-linked with seizures, short stature and midface hypoplasia", "MENTAL RETARDATION, X-LINKED, WITH SEIZURES, SHORT STATURE, AND MIDFACE HYPOPLASIA", "Mental Retardation, X-Linked, with Seizures, Short Stature, and Midface Hypoplasia", "mental retardation, X-linked, with seizures, short stature, and midface hypoplasia", "intellectual disability, X-linked with seizures, short stature and midface hypoplasia", "intellectual disability, X-linked, with seizures, short stature, and midface hypoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "creatine transporter deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0017074", "names": ["cervicothoracic spina bifida cystica"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervicothoracic spina bifida cystica", "shortest_name_length": 36}
{"curie": "MONDO:0007244", "names": ["CAFYD", "Caffey", "Caffey Disease", "caffey disease", "CAFFEY DISEASE", "Caffey disease", "Caffey syndrome", "Disease, Caffey", "caffey syndrome", "Caffey's disease", "Coffey's disease", "caffey's disease", "Familial Caffey Disease", "Familial Caffeys Disease", "Familial Caffey's Disease", "Caffey's Disease, Familial", "Disease, Familial Caffey's", "Canine cortical hyperostosis", "infantile cortical hyperostosis", "Infantile Cortical Hyperostosis", "INFANTILE CORTICAL HYPEROSTOSIS", "Infantile Cortical Hyperostoses", "Infantile cortical hyperostoses", "Infantile cortical hyperostosis", "Hyperostoses, Infantile Cortical", "Hyperostosis, Infantile Cortical", "Cortical Hyperostoses, Infantile", "cortical congenital hyperostosis", "Cortical Congenital Hyperostoses", "Cortical Hyperostosis, Infantile", "Hyperostosis, infantile cortical", "Cortical Congenital Hyperostosis", "Congenital Cortical Hyperostosis", "Congenital Cortical Hyperostoses", "Hyperostoses, Congenital Cortical", "Cortical Hyperostoses, Congenital", "Congenital Hyperostosis, Cortical", "Congenital Hyperostoses, Cortical", "Hyperostosis, Cortical Congenital", "Cortical Hyperostosis, Congenital", "Hyperostoses, Cortical Congenital", "cortical; hyperostosis, infantile", "hyperostosis; cortical, infantile", "Hyperostosis, Congenital Cortical", "Caffey-De Toni-Silvermann Syndrome", "Caffey De Toni Silvermann Syndrome", "Hyperostosis, Cortical, Congenital", "Syndrome, Caffey-De Toni-Silvermann", "Familial Infantile Cortical Hyperostosis", "Familial infantile cortical hyperostosis", "Infantile cortical hyperostosis (disorder)", "infantile cortical hyperostosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Caffey disease", "shortest_name_length": 5}
{"curie": "MONDO:0010021", "names": ["Bfns, autosomal recessive", "BFNS, AUTOSOMAL RECESSIVE", "Epilepsy, Benign Neonatal, Autosomal Recessive", "convulsions benign familial neonatal dominant form", "autosomal dominant form of benign neonatal seizures", "Seizures, Benign Familial Neonatal, Autosomal Recessive", "EPILEPSY, BENIGN FAMILIAL NEONATAL, AUTOSOMAL RECESSIVE", "epilepsy, benign familial neonatal, autosomal recessive", "seizures, benign familial neonatal, autosomal recessive", "SEIZURES, BENIGN FAMILIAL NEONATAL, AUTOSOMAL RECESSIVE", "convulsions, benign familial neonatal, autosomal recessive", "CONVULSIONS, BENIGN FAMILIAL NEONATAL, AUTOSOMAL RECESSIVE", "Convulsions, Benign Familial Neonatal, Autosomal Recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "seizures, benign familial neonatal, autosomal recessive", "shortest_name_length": 25}
{"curie": "UMLS:C4727405", "names": ["Recurrent Skin Angiosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Skin Angiosarcoma", "shortest_name_length": 27}
{"curie": "MONDO:0024421", "names": ["Hennekam Koss de Geest syndrome", "short stature contractures hypotonia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short stature contractures hypotonia", "shortest_name_length": 31}
{"curie": "UMLS:C0751925", "names": ["nerve palsy sciatic", "Sciatic Nerve Palsy", "SCIATIC NERVE PALSY", "Sciatic nerve palsy", "sciatic nerve palsy", "Palsy, Sciatic Nerve", "Nerve Palsy, Sciatic", "Sciatic Nerve Palsies", "Palsies, Sciatic Nerve", "Nerve Palsies, Sciatic", "Sciatic nerve palsy (disorder)", "sciatic nerve palsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sciatic Nerve Palsy", "shortest_name_length": 19}
{"curie": "MONDO:0017305", "names": ["syndromic oculocutaneous albinism", "syndrome associated with oculocutaneous albinism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic oculocutaneous albinism", "shortest_name_length": 33}
{"curie": "MONDO:0012024", "names": ["RP26", "RP 26", "RETINITIS PIGMENTOSA 26", "Retinitis Pigmentosa 26", "retinitis pigmentosa 26", "CERKL retinitis pigmentosa", "retinitis pigmentosa type 26", "retinitis pigmentosa caused by mutation in CERKL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 26", "shortest_name_length": 4}
{"curie": "MONDO:0008344", "names": ["HAPH", "high altitude pulmonary edema", "High altitude pulmonary edema", "High altitude pulmonary oedema", "Pulmonary edema of mountaineers", "pulmonary edema of mountaineers", "Pulmonary oedema of mountaineers", "HIGH ALTITUDE PULMONARY HYPERTENSION", "High altitude pulmonary hypertension", "high altitude pulmonary hypertension", "High altitude pulmonary edema (disorder)", "high altitude pulmonary edema (diagnosis)", "High altitude pulmonary hypertension (disorder)", "PULMONARY EDEMA OF MOUNTAINEERS, SUSCEPTIBILITY TO", "pulmonary edema of mountaineers, susceptibility to", "Pulmonary hypertension due to chronic exposure to high altitude"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary edema of mountaineers, susceptibility to", "shortest_name_length": 4}
{"curie": "MONDO:0014948", "names": ["SSMG", "SRMMD", "SHORT STATURE-MICROGNATHIA SYNDROME", "SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY", "short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay", "short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay; SRMMD"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay", "shortest_name_length": 4}
{"curie": "UMLS:C1723764", "names": ["prostatitis chronic - chronic pelvic pain syndrome", "Chronic prostatitis - chronic pelvic pain syndrome", "Chronic Prostatitis with Chronic Pelvic Pain Syndrome", "Chronic prostatitis - chronic pelvic pain syndrome (disorder)", "prostatitis chronic - chronic pelvic pain syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic Prostatitis with Chronic Pelvic Pain Syndrome", "shortest_name_length": 50}
{"curie": "MONDO:0001122", "names": ["chronic antritis", "Chronic antritis", "Antritis (chronic)", "Chronic maxillary antritis", "MAXILLARY SINUSITIS CHRONIC", "chronic maxillary sinusitis", "Chronic maxillary sinusitis", "Chronic Maxillary Sinusitis", "maxillary sinusitis, chronic", "Chronic maxillary sinusitis (disorder)", "chronic maxillary sinusitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic maxillary sinusitis", "shortest_name_length": 16}
{"curie": "UMLS:C1336020", "names": ["Soft Palate Benign Mixed Tumor", "Soft Palate Pleomorphic Adenoma", "Benign Mixed Tumor of Soft Palate", "Pleomorphic Adenoma of Soft Palate", "Benign Mixed Tumor of the Soft Palate", "Pleomorphic Adenoma of the Soft Palate", "Soft Palate Benign Mixed Salivary Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Soft Palate Pleomorphic Adenoma", "shortest_name_length": 30}
{"curie": "UMLS:C5205728", "names": ["Prostate Osteosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Osteosarcoma", "shortest_name_length": 21}
{"curie": "MONDO:0019356", "names": ["urogenital tract malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urogenital tract malformation", "shortest_name_length": 29}
{"curie": "UMLS:C0686597", "names": ["Lymphoid leukemia in remission", "Lymphoid Leukemia in Remission", "Lymphoid leukaemia in remission", "Lymphoid leukemia (in remission)", "Lymphoid Leukemia (in Remission)", "lymphocytic leukemia in remission", "leukemia lymphocytic in remission", "Lymphoid leukaemia (in remission)", "Lymphoid leukemia, NOS, in remission", "Lymphoid leukaemia, NOS, in remission", "Lymphoid leukemia in remission (disorder)", "Unspecified lymphoid leukemia in remission", "Unspecified lymphoid leukemia, in remission", "Unspecified lymphoid leukaemia in remission", "Lymphoid leukemia, unspecified, in remission", "lymphocytic leukemia in remission (diagnosis)", "Lymphoid leukaemia, unspecified, in remission"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoid leukemia in remission", "shortest_name_length": 30}
{"curie": "UMLS:C0338750", "names": ["episodic hallucinogen dependence", "Hallucinogen dependence, episodic", "Hallucinogen Dependence, Episodic Use", "Hallucinogen dependence, episodic use", "episodic hallucinogen dependence (diagnosis)", "Hallucinogen dependence, episodic (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hallucinogen dependence, episodic", "shortest_name_length": 32}
{"curie": "UMLS:C5419743", "names": ["Advanced Kidney Medullary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Kidney Medullary Carcinoma", "shortest_name_length": 35}
{"curie": "MONDO:0007810", "names": ["ICHTHYOSIS SIMPLEX", "Ichthyosis simplex", "Ichthyosis Simplex", "ichthyosis simplex", "ichthyosis; simplex", "ICHTHYOSIS VULGARIS", "simplex; ichthyosis", "ichthyosis vulgaris", "Ichthyosis vulgaris", "Ichthyosis Vulgaris", "vulgaris; ichthyosis", "Ichthyosis Simplices", "ichthyosis; vulgaris", "Dominant Ichthyosis Vulgaris", "dominant ichthyosis vulgaris", "Dominant ichthyosis vulgaris", "Ichthyosis Vulgaris, Dominant", "Ichthyosis vulgaris, dominant", "Ichthyosis vulgaris (disorder)", "ichthyosis vulgaris (diagnosis)", "autosomal dominant ichthyosis vulgaris", "ichthyosis vulgaris, autosomal dominant", "dominant congenital ichthyosiform erythroderma", "Dominant congenital ichthyosiform erythroderma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant ichthyosis vulgaris", "shortest_name_length": 18}
{"curie": "MONDO:0002846", "names": ["granulomatous gastritis", "Granulomatous gastritis", "Granulomatous Gastritis", "granulomatous; gastritis", "gastritis; granulomatous"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "granulomatous gastritis", "shortest_name_length": 23}
{"curie": "MONDO:0001706", "names": ["neurosarcoidosis", "Cerebral Sarcoidosis", "cerebral sarcoidosis", "Cerebral sarcoidosis", "telencephalon sarcoidosis", "sarcoidosis of telencephalon", "Cerebral sarcoidosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral sarcoidosis", "shortest_name_length": 16}
{"curie": "MONDO:0006782", "names": ["hemometra", "Hemometra", "Haemometra", "hematometra", "Hematometra", "HEMATOMETRA", "HAEMATOMETRA", "Hematometras", "Haematometra", "haematometra", "Hematometra (disorder)", "hematometra (diagnosis)", "hemorrhage; intrauterine", "intrauterine; hemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemometra", "shortest_name_length": 9}
{"curie": "UMLS:C0007098", "names": ["Walker Carcinoma 256", "Walker carcinoma 256", "Carcinoma 256, Walker", "Walker Carcinosarcoma 256", "Carcinosarcoma 256, Walker"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carcinoma 256, Walker", "shortest_name_length": 20}
{"curie": "UMLS:C1336122", "names": ["Stage IA Ovarian Germ Cell Tumor", "stage IA ovarian germ cell tumor", "Stage IA Ovarian Germ Cell Tumor AJCC v6", "Stage IA Ovarian Germ Cell Tumor AJCC v7", "FIGO Stage IA Malignant Ovarian Germ Cell Tumor", "Stage IA Ovarian Germ Cell Tumor AJCC v6 and v7", "FIGO Stage IA Malignant Germ Cell Tumor of Ovary", "FIGO Stage IA Malignant Ovarian Germ Cell Neoplasm", "FIGO Stage IA Malignant Germ Cell Neoplasm of Ovary", "FIGO Stage IA Malignant Germ Cell Tumor of the Ovary", "FIGO Stage IA Malignant Germ Cell Neoplasm of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Ovarian Germ Cell Tumor AJCC v6 and v7", "shortest_name_length": 32}
{"curie": "MONDO:0001816", "names": ["Scleroperikeratitis", "scleroperikeratitis", "scleroperikeratitis (diagnosis)", "scleritis with corneal involvement", "Scleritis with corneal involvement", "Scleritis with corneal involvement (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scleroperikeratitis", "shortest_name_length": 19}
{"curie": "MONDO:0001612", "names": ["stenosis carotid", "Carotid Stenoses", "Carotid stenosis", "carotid stenoses", "carotid stenosis", "Carotid Stenosis", "CAROTID STENOSIS", "Stenoses, Carotid", "Stenosis, Carotid", "artery carotid stenosi", "carotid artery stenosis", "artery carotid stenosis", "Stenosis;artery;carotid", "Carotid Artery Stenosis", "Carotid artery stenosis", "stenosis carotid artery", "Carotid Artery Stenoses", "Carotid artery--Stenosis", "Stenosis, carotid artery", "Carotid Artery Narrowing", "carotid artery narrowing", "Stenoses, Carotid Artery", "Stenosis, Carotid Artery", "Artery Stenosis, Carotid", "Carotid artery narrowing", "Artery Stenoses, Carotid", "stenosis, carotid artery", "Narrowing, Carotid Artery", "Artery Narrowing, Carotid", "arteries carotid stenosis", "Carotid Artery Narrowings", "Artery Narrowings, Carotid", "Narrowings, Carotid Artery", "arteries carotid narrowing", "Narrowing of carotid artery", "Carotid artery stenosis (disorder)", "carotid artery stenosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carotid stenosis", "shortest_name_length": 16}
{"curie": "UMLS:C1112734", "names": ["Gastric infection", "gastric infection", "Gastric Infection", "gastric infections"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric infection", "shortest_name_length": 17}
{"curie": "UMLS:C1698096", "names": ["Urostomy Prolapse", "Prolapse of urostomy", "Prolapse of urostomy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urostomy Prolapse", "shortest_name_length": 17}
{"curie": "MONDO:0014098", "names": ["FPLD5", "CIDEC-related FPLD", "familial partial lipodystrophy type 5", "LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 5", "lipodystrophy, familial partial, type 5", "CIDEC-related familial partial lipodystrophy", "FPLD5 - familial partial lipodystrophy type 5", "familial partial lipodystrophy associated with CIDEC mutations", "lipodystrophy, familial partial, associated with Cidec mutations", "LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH CIDEC MUTATIONS", "Cell death inducing DFFA like effector C-related familial partial lipodystrophy", "Cell death inducing DFFA like effector C-related familial partial lipodystrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CIDEC-related familial partial lipodystrophy", "shortest_name_length": 5}
{"curie": "MONDO:0007706", "names": ["sternal nonunion with supraumbilical raphe", "Sternal nonunion with supraumbilical raphe", "STERNAL NONUNION WITH SUPRAUMBILICAL RAPHE", "Hemangiomas cavernous of face supraumbilical midline raphe", "hemangiomas cavernous of face supraumbilical midline raphe", "Cavernous hemangiomas of face and supraumbilical midline raphe", "Cavernous haemangiomas of face and supraumbilical midline raphe", "Raphe, supraumbilical midline, with cavernous facial hemangiomas", "hemangiomas, cavernous, of face and supraumbilical MIDLINE raphe", "HEMANGIOMAS, CAVERNOUS, OF FACE AND SUPRAUMBILICAL MIDLINE RAPHE", "Hemangiomas, Cavernous, of Face and Supraumbilical Midline Raphe", "RAPHE, SUPRAUMBILICAL MIDLINE, WITH CAVERNOUS FACIAL HEMANGIOMAS", "raphe, supraumbilical Midline, with cavernous Facial hemangiomas", "supraumbilical midabdominal raphe and facial cavernous hemangiomas", "Supraumbilical midabdominal raphe and facial cavernous hemangiomas", "cavernous hemangiomas of face-supraumbilical midline raphe syndrome", "Cavernous hemangiomas of face and supraumbilical midline raphe (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cavernous hemangiomas of face-supraumbilical midline raphe syndrome", "shortest_name_length": 42}
{"curie": "MONDO:0017983", "names": ["humero-radio-ulnar fusion", "humero-radio-ulnar synostosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "humero-radio-ulnar synostosis", "shortest_name_length": 25}
{"curie": "UMLS:C5205911", "names": ["Prostate Hemangioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Hemangioma", "shortest_name_length": 19}
{"curie": "UMLS:C0267920", "names": ["RPC", "Cholangiohepatitis", "Oriental cholangiohepatitis", "Recurrent Pyogenic Cholangitis", "Recurrent pyogenic cholangitis", "Recurrent pyogenic cholangitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent pyogenic cholangitis", "shortest_name_length": 3}
{"curie": "UMLS:C1704291", "names": ["Primary Bone Osteosarcoma", "Primary Osteosarcoma of Bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Bone Osteosarcoma", "shortest_name_length": 25}
{"curie": "MONDO:0001388", "names": ["glans penis cancer", "cancer of glans penis", "Cancer of glans penis", "Malignant tumor of glans penis", "malignant glans penis neoplasm", "malignant tumor of glans penis", "malignant tumour of glans penis", "Malignant tumour of glans penis", "malignant neoplasm of glans penis", "Malignant neoplasm of glans penis", "penile neoplasm malignant glans penis", "Malignant tumor of glans penis (disorder)", "malignant neoplasm of glans penis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glans penis cancer", "shortest_name_length": 18}
{"curie": "MONDO:0014009", "names": ["ARCI7", "autosomal recessive congenital ichthyosis 7", "ichthyosis, congenital, autosomal recessive 7", "ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 7", "autosomal recessive congenital ichthyosis type 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive congenital ichthyosis 7", "shortest_name_length": 5}
{"curie": "MONDO:0008554", "names": ["THCYT1", "THROMBOCYTOSIS 1", "thrombocytosis 1", "THROMBOCYTHEMIA 1", "thrombocythemia 1", "thrombocythemia type 1", "thrombocythemia, somatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombocythemia 1", "shortest_name_length": 6}
{"curie": "UMLS:C0259795", "names": ["radiation enteritis", "enteritis radiation", "Radiation enteritis", "Radiation Enteritis", "enteritis due to radiation", "Enteritis due to radiation", "Radiation induced enteritis", "Enteritis caused by radiation", "Radiation enteritis of intestine", "enteritis due to radiation (diagnosis)", "Inflammation of intestine caused by radiation", "Inflammation of intestine caused by radiation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radiation enteritis of intestine", "shortest_name_length": 19}
{"curie": "MONDO:0010074", "names": ["BCYM1B", "Toledo type brachyolmia", "Brachyolmia, Toledo type", "Sed, chondroitin sulfate type", "SED, Chondroitin Sulfate Type", "SED, CHONDROITIN SULFATE TYPE", "BRACHYOLMIA TYPE 1, TOLEDO TYPE", "Brachyolmia type 1, Toledo type", "Brachyolmia Type 1, Toledo Type", "brachyolmia type 1, Toledo type", "brachyolmia type 1, toledo type", "SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, TOLEDO TYPE", "Spondyloepiphyseal dysplasia tarda, Toledo type", "spondyloepiphyseal dysplasia tarda, Toledo type", "PAPS-chondroitin sulfate sulfotransferase deficiency", "Paps-Chondroitin Sulfate Sulfotransferase Deficiency", "PAPS-CHONDROITIN SULFATE SULFOTRANSFERASE DEFICIENCY", "Spondyloepiphyseal dysplasia, chondroitin sulfate type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachyolmia type 1, toledo type", "shortest_name_length": 6}
{"curie": "MONDO:0023100", "names": ["facial clefting corpus callosum agenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "facial clefting corpus callosum agenesis", "shortest_name_length": 40}
{"curie": "MONDO:0014969", "names": ["SHPKD", "Isolated SHPK deficiency", "isolated SHPK deficiency", "Deficiency of heptulokinase", "sedoheptulokinase deficiency", "SEDOHEPTULOKINASE DEFICIENCY", "Deficiency of sedoheptulokinase", "isolated sedoheptulokinase deficiency", "Isolated sedoheptulokinase deficiency", "Deficiency of sedoheptulokinase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated sedoheptulokinase deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C4727172", "names": ["Unresectable Chordoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Chordoma", "shortest_name_length": 21}
{"curie": "UMLS:C1696943", "names": ["Hypoesthesia facial", "Hypoaesthesia facial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypoaesthesia facial", "shortest_name_length": 19}
{"curie": "MONDO:0017309", "names": ["neonatal MFS", "Neonatal MFS", "Neonatal Marfan syndrome", "neonatal Marfan syndrome", "MARFAN SYNDROME, NEONATAL", "Neonatal Marfan syndrome (disorder)", "Neonatal Marfan syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal Marfan syndrome", "shortest_name_length": 12}
{"curie": "UMLS:C5555712", "names": ["Recurrent Malignant Spermatic Cord Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Malignant Spermatic Cord Neoplasm", "shortest_name_length": 43}
{"curie": "UMLS:C0281913", "names": ["muscle swelling", "Muscle swelling", "Muscle Swelling", "swelling muscle", "muscles swelling", "Swelling;muscle(s)", "Swelling of skeletal muscle", "Swelling of skeletal muscle (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Swelling of skeletal muscle", "shortest_name_length": 15}
{"curie": "UMLS:C1736172", "names": ["Acute cytolytic hepatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute cytolytic hepatitis", "shortest_name_length": 25}
{"curie": "MONDO:0042496", "names": ["Ergotism", "ergotism", "ergotisms", "ergot poisoning", "poisoning, ergot", "St. Anthony fire", "ergot poisonings", "poisonings, ergot", "St. Anthonys fire", "St Anthony's fire", "Saint Anthony fire", "fire, St. Anthonys", "St. Anthony's fire", "Saint Anthonys fire", "Saint Anthony's fire"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ergotism", "shortest_name_length": 8}
{"curie": "MONDO:0004909", "names": ["urethra abscess", "URETHRA ABSCESS", "Urethral abscess", "urethra; abscess", "urethral abscess", "abscess; urethra", "Urethral abscess, NOS", "Urethral gland abscess", "urethral gland abscess", "Abscess of urethral gland", "Urethral gland abscess, NOS", "Urethral abscess (disorder)", "urethral abscess (diagnosis)", "Abscess (of) urethral (gland)", "Abscess of urethral gland (disorder)", "Abscess of urethral gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urethral gland abscess", "shortest_name_length": 15}
{"curie": "UMLS:C3711125", "names": ["Mitochondrial DNA Depletion Syndrome 8A", "Mitochondrial Dna Depletion Syndrome, Encephalomyopathic Form, With Renal Tubulopathy, Autosomal Recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mitochondrial DNA Depletion Syndrome 8A", "shortest_name_length": 39}
{"curie": "UMLS:C5419758", "names": ["Unresectable Laryngeal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Laryngeal Squamous Cell Carcinoma", "shortest_name_length": 46}
{"curie": "MONDO:0008303", "names": ["FMPP", "testotoxicosis", "Testotoxicosis", "pubertas praecox", "Familial testotoxicosis", "Familial Testotoxicosis", "testotoxicosis, familial", "precocious puberty, male", "TESTOTOXICOSIS, FAMILIAL", "Precocious Pseudopuberty", "Testotoxicosis, Familial", "Male-limited precocious puberty", "male-limited precocious puberty", "Male-Limited Precocious Puberty", "precocious puberty, male limited", "Puberty, Male-Limited Precocious", "PRECOCIOUS PUBERTY, MALE-LIMITED", "precocious puberty, male-limited", "Precocious Puberty, Male-Limited", "Precocious Puberty, Male Limited", "familial Testotoxicosis (subtype)", "Male-Limited Precocious Puberties", "Precocious Puberties, Male-Limited", "Puberties, Male-Limited Precocious", "LHCGR peripheral precocious puberty", "Familial male-limited precocious puberty", "Familial Male-Limited Precocious Puberty", "familial male-limited precocious puberty", "Gonadotrophin-Independent Precocious Puberty", "Gonadotrophin-independent male sexual precocity", "Gonadotropin-independent familial sexual precocity", "Familial Gonadotrophin-Independent Sexual Precocity", "Familial male-limited precocious puberty (disorder)", "Sexual precocity, familial, gonadotropin-independent", "SEXUAL PRECOCITY, FAMILIAL, GONADOTROPIN-INDEPENDENT", "sexual precocity, familial, gonadotropin-independent", "leydig cell adenoma, somatic, with precocious puberty", "peripheral precocious puberty caused by mutation in LHCGR", "Familial gonadotropin-independent male-limited sexual precocity", "familial gonadotropin-independent male-limited sexual precocity", "Leydig Cell Adenoma, Somatic, with Male-Limited Precocious Puberty", "Leydig cell adenoma, somatic, with male-limited precocious puberty", "LEYDIG CELL ADENOMA, SOMATIC, WITH MALE-LIMITED PRECOCIOUS PUBERTY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial male-limited precocious puberty", "shortest_name_length": 4}
{"curie": "MONDO:0010874", "names": ["Enteropathy, Familial, with Villous Edema and Immunoglobulin G2 Deficiency", "ENTEROPATHY, FAMILIAL, WITH VILLOUS EDEMA AND IMMUNOGLOBULIN G2 DEFICIENCY", "enteropathy, familial, with villous edema and immunoglobulin G2 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "enteropathy, familial, with villous edema and immunoglobulin G2 deficiency", "shortest_name_length": 74}
{"curie": "MONDO:0004296", "names": ["cervical lymphoepithelioma-like carcinoma", "Cervical Lymphoepithelioma-Like Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical lymphoepithelioma-like carcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0005743", "names": ["Encephalitozoonoses", "Encephalitozoonosis", "encephalitozoonosis", "Infection by Encephalitozoon", "infection by Encephalitozoon", "Infection by Encephalitozoon, NOS", "Infection caused by Encephalitozoon", "Infection caused by Encephalitozoon (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephalitozoonosis", "shortest_name_length": 19}
{"curie": "UMLS:C1336284", "names": ["stage II extragonadal non-seminomatous germ cell tumor", "Stage II Extragonadal Non-Seminomatous Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Extragonadal Non-Seminomatous Germ Cell Tumor", "shortest_name_length": 54}
{"curie": "UMLS:C0342483", "names": ["Hyperreninemic Hypoaldosteronism", "Hyperreninemic hypoaldosteronism", "Hyperreninaemic hypoaldosteronism", "Hyperreninemic hypoaldosteronism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyperreninemic hypoaldosteronism", "shortest_name_length": 32}
{"curie": "MONDO:0014164", "names": ["MKS11", "meckel syndrome 11", "TMEM231 Meckel syndrome", "Meckel syndrome type 11", "Meckel syndrome, type 11", "MECKEL SYNDROME, TYPE 11", "Meckel syndrome type 11 (diagnosis)", "Meckel syndrome caused by mutation in TMEM231"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meckel syndrome, type 11", "shortest_name_length": 5}
{"curie": "MONDO:0009622", "names": ["JWDS", "KELLY SYNDROME", "JAWAD SYNDROME", "Jawad syndrome", "Kelly syndrome", "JAWAD syndrome", "Jawad Syndrome", "Jawad syndrome (disorder)", "Jawad syndrome (diagnosis)", "microcephaly-digital anomalies syndrome", "MICROCEPHALY WITH MENTAL RETARDATION AND DIGITAL ANOMALIES", "microcephaly with mental retardation and digital anomalies", "Microcephaly with Mental Retardation and Digital Anomalies", "microcephaly with intellectual disability and digital anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jawad syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C5445178", "names": ["Intraductal and lobular carcinoma", "Intraductal and Lobular Carcinoma", "Breast Intraductal and Lobular Carcinoma", "Breast Ductal Carcinoma In Situ and Lobular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Ductal Carcinoma In Situ and Lobular Carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0008757", "names": ["AU", "ALUNC", "Alopecia, complete", "Universal alopecia", "ALOPECIA UNIVERSALIS", "Generalized Atrichia", "Alopecia universalis", "alopecia universalis", "alopecia; universalis", "universalis; alopecia", "ATRICHIA, GENERALIZED", "atrichia, generalized", "Atrichia, Generalized", "Universal alopecia areata", "alopecia areata universalis", "alopecia universalis congenita", "ALOPECIA UNIVERSALIS CONGENITA", "Alopecia universalis congenita", "Alopecia universalis (disorder)", "alopecia universalis (diagnosis)", "ALUNC Alopecia universalis congenitalis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alopecia universalis congenita", "shortest_name_length": 2}
{"curie": "MONDO:0020787", "names": ["HOMGSMR1", "hypomagnesemia, seizures, and mental retardation", "HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION 1", "hypomagnesemia, seizures, and intellectual disability 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypomagnesemia, seizures, and intellectual disability 1", "shortest_name_length": 8}
{"curie": "MONDO:0001187", "names": ["bladder ca", "BLADDER CANCER", "Bladder Cancer", "bladder cancer", "Bladder cancer", "Bladder Cancers", "bladder cancers", "Cancer, Bladder", "Bladder--Cancer", "Cancer of Bladder", "cancer of bladder", "Cancer of bladder", "Bladder cancer NOS", "CA - Bladder cancer", "tumor of the bladder", "cancer of the bladder", "Cancer of the Bladder", "urinary bladder cancer", "Neoplasm malig;bladder", "Urinary Bladder Cancer", "malignant bladder tumor", "Malignant Bladder Tumor", "bladder cancer, somatic", "Cancer, Urinary Bladder", "BLADDER CANCER MALIGNANT", "cancer of urinary bladder", "malignant bladder neoplasm", "Malignant Bladder Neoplasm", "malignant tumor of bladder", "Malignant Tumor of Bladder", "bladder cancer (diagnosis)", "malignant neoplasm, bladder", "Bladder neoplasms malignant", "Malignant Neoplasm, Bladder", "malignant neoplasm of bladder", "Malignant neoplasm of bladder", "Malignant Neoplasm of Bladder", "malignant tumor of the bladder", "Malignant Tumor of the Bladder", "Malignant Urinary Bladder Tumor", "malignant urinary bladder tumor", "urinary bladder malignant tumor", "Urinary Bladder Malignant Tumor", "malignant tumor, urinary bladder", "Malignant Tumor, Urinary Bladder", "Malignant Neoplasm of the Bladder", "malignant neoplasm of the bladder", "malignant urinary bladder neoplasm", "malignant tumor of urinary bladder", "Malignant neoplasm of bladder, NOS", "urinary bladder malignant neoplasm", "Malignant Urinary Bladder Neoplasm", "Malignant Tumor of Urinary Bladder", "Malignant tumor of urinary bladder", "malignant neosplasm of the bladder", "Urinary Bladder Malignant Neoplasm", "Malignant tumour of urinary bladder", "Malignant Neoplasm, Urinary Bladder", "malignant neoplasm, urinary bladder", "malignant neoplasm of urinary bladder", "Malignant neoplasm of urinary bladder", "Malignant Neoplasm of Urinary Bladder", "malignant tumor of the urinary bladder", "Malignant Tumor of the Urinary Bladder", "Malignant Neoplasm of the Urinary Bladder", "malignant neoplasm of the urinary bladder", "malignant neoplasm of bladder (diagnosis)", "Malignant neoplasm of bladder, unspecified", "Malignant tumor of urinary bladder (disorder)", "Malignant neoplasm of bladder, part unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urinary bladder cancer", "shortest_name_length": 10}
{"curie": "UMLS:C5204343", "names": ["Borderline Ovarian Mucinous Tumor/Atypical Proliferative Ovarian Mucinous Tumor with Microinvasion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Ovarian Mucinous Tumor/Atypical Proliferative Ovarian Mucinous Tumor with Microinvasion", "shortest_name_length": 98}
{"curie": "MONDO:0018739", "names": ["Isoimmune neonatal neutropenia", "Neonatal isoimmune neutropenia", "neutropenia alloimmune neonatal", "Neonatal alloimmune neutropenia", "Alloimmune neonatal neutropenia", "neonatal alloimmune neutropenia", "Alloimmune neonatal neutropenia (disorder)", "Alloimmune neonatal neutropenia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal alloimmune neutropenia", "shortest_name_length": 30}
{"curie": "UMLS:C3899674", "names": ["Brain Oligodendroglioma", "Childhood Brain Oligodendroglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Brain Oligodendroglioma", "shortest_name_length": 23}
{"curie": "UMLS:C1335039", "names": ["Non-Neoplastic Retinal Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Retinal Disorder", "shortest_name_length": 31}
{"curie": "MONDO:0004236", "names": ["Duodenal Somatostatinoma", "duodenal somatostatinoma", "Duodenal Somatostatin-Producing NET", "duodenal somatostatin-producing NET", "duodenal somatostatin producing tumor", "Duodenal Somatostatin Producing Tumor", "duodenal delta cell somatostatin producing tumor", "duodenal somatostatin-producing neuroendocrine tumor", "Duodenal Somatostatin-Producing Neuroendocrine Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "duodenal somatostatinoma", "shortest_name_length": 24}
{"curie": "UMLS:C3273074", "names": ["Liver Lymphangiomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liver Lymphangiomatosis", "shortest_name_length": 23}
{"curie": "UMLS:C0010046", "names": ["corn", "Corn", "corns", "Corns", "Clavus", "clavus", "corning", "corn toe", "corn toes", "corns toe", "corns toes", "Corn of toe", "corn of toe", "Corn - lesion", "corns (diagnosis)", "Corn of toe (disorder)", "Corn - lesion (disorder)", "corn of toe (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Corn of toe", "shortest_name_length": 4}
{"curie": "MONDO:0006539", "names": ["Diffuse Lipomatosis", "diffuse lipomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diffuse lipomatosis", "shortest_name_length": 19}
{"curie": "MONDO:0007451", "names": ["NDI2", "diabetes insipidus, nephrogenic, 2", "nephrogenic diabetes insipidus type 2", "diabetes insipidus, nephrogenic, type 2", "Nephrogenic Diabetes Insipidus, Type II", "DIABETES INSIPIDUS, NEPHROGENIC, TYPE II", "Diabetes Insipidus, Nephrogenic, Type II", "nephrogenic diabetes insipidus, autosomal", "autosomal nephrogenic diabetes insipidus-2", "diabetes insipidus, nephrogenic, autosomal", "Diabetes Insipidus, Nephrogenic, Autosomal", "DIABETES INSIPIDUS, NEPHROGENIC, 2, AUTOSOMAL", "nephrogenic diabetes insipidus, autosomal (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diabetes insipidus, nephrogenic, autosomal", "shortest_name_length": 4}
{"curie": "MONDO:0001020", "names": ["Lazy Eye", "Lazy eye", "lazy eye", "amblyopic", "AMBLYOPIA", "amblyopia", "Amblyopic", "Amblyopia", "Amblyopias", "Amblyopia NOS", "Wandering eye", "Wandering eyes", "Amblyopia, NOS", "amblyopia (disease)", "Amblyopia (disorder)", "amblyopia (diagnosis)", "Unspecified amblyopia", "Amblyopia, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amblyopia", "shortest_name_length": 8}
{"curie": "UMLS:C4528177", "names": ["Recurrent High Risk Myelodysplastic Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent High Risk Myelodysplastic Syndrome", "shortest_name_length": 44}
{"curie": "UMLS:C4682753", "names": ["IIIB", "Stage IIIB Prostate Cancer", "stage IIIB prostate cancer", "Stage IIIB Prostate Cancer AJCC v8", "stage IIIB prostate cancer AJCC v8", "Stage IIIB Prostate Carcinoma AJCC v8", "stage IIIB prostate carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Prostate Cancer AJCC v8", "shortest_name_length": 4}
{"curie": "UMLS:C1257931", "names": ["Human Mammary Neoplasm", "Human Mammary Neoplasms", "Neoplasm, Human Mammary", "Mammary Neoplasm, Human", "Mammary Neoplasms, Human", "Neoplasms, Human Mammary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mammary Neoplasms, Human", "shortest_name_length": 22}
{"curie": "MONDO:0006751", "names": ["Rosenbach", "erysipelothrix", "Erysipelothrix", "Erysipelothrix disease", "Erysipelothrix Infection", "Erysipelothrix (disease)", "Erysipelothrix infection", "Infection, Erysipelothrix", "Erysipelothrix Infections", "infection, Erysipelothrix", "Erysipelothrix; infection", "Erysipelothrix infections", "ERYSIPELOTHRIX INFECTIONS", "infection; Erysipelothrix", "Infections, Erysipelothrix", "infections, Erysipelothrix", "Erysipelothrix infectious disease", "Erysipelothrix disease (disorder)", "Erysipelothrix disease or disorder", "listeriosis erysipelothrix infection", "Erysipelothrix infection (diagnosis)", "Erysipelothrix caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Erysipelothrix infectious disease", "shortest_name_length": 9}
{"curie": "UMLS:C4526859", "names": ["Relapsed Cervical Adenocarcinoma", "Recurrent Cervical Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Cervical Adenocarcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C3203523", "names": ["Serial seizure", "Seizure cluster", "Serial seizures", "Cluster seizure", "Cluster seizures", "Seizure flurries", "Crescendo seizure", "Cyclical seizures", "Recurrent seizure", "SEIZURE RECURRENT", "Recurrent seizures", "Crescendo seizures", "Recurrent seizures NOS", "Acute repetitive seizure", "Acute repetitive seizures", "Cluster seizures (finding)", "Recurrent seizure (disorder)", "Acute repetitive seizure (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute repetitive seizure", "shortest_name_length": 14}
{"curie": "MONDO:0002086", "names": ["Degos Acanthoma", "Degos acanthoma", "Degos' acanthoma", "Acanthoma, Degos", "clear cell acanthoma", "Clear Cell Acanthoma", "Clear cell acanthoma", "Acanthoma, Clear Cell", "Clear Cell Acanthomas", "Acanthomas, Clear Cell", "Pale (Clear Cell) Acanthoma", "Pale (Clear cell) acanthoma", "pale (clear cell) acanthoma", "Clear cell acanthoma of Degos", "Clear cell acanthoma (disorder)", "Clear cell acanthoma (morphologic abnormality)", "clear cell acanthoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "clear cell acanthoma", "shortest_name_length": 15}
{"curie": "UMLS:C1333005", "names": ["Pediatric Systemic Anaplastic Large Cell Lymphoma", "Childhood Systemic Anaplastic Large Cell Lymphoma", "Childhood Systemic K-1+ Anaplastic Large Cell Lymphoma", "Pediatric Systemic K-1+ Anaplastic Large Cell Lymphoma", "Pediatric Systemic CD30+ Anaplastic Large Cell Lymphoma", "Childhood Systemic CD30+ Anaplastic Large Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Systemic Anaplastic Large Cell Lymphoma", "shortest_name_length": 49}
{"curie": "MONDO:0020378", "names": ["early-onset posterior polar cataract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early-onset posterior polar cataract", "shortest_name_length": 36}
{"curie": "UMLS:C2721733", "names": ["Mesenteritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mesenteritis", "shortest_name_length": 12}
{"curie": "UMLS:C2011252", "names": ["Giant cell carcinoma of larynx", "Laryngeal Giant Cell Carcinoma", "Laryngeal Anaplastic Carcinoma", "giant cell carcinoma of larynx", "Giant cell carcinoma of larynx (disorder)", "giant cell carcinoma of larynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laryngeal Giant Cell Carcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0013909", "names": ["HHV8S", "HHV-8, susceptibility to", "HHV-8, SUSCEPTIBILITY TO", "HUMAN HERPESVIRUS 8, SUSCEPTIBILITY TO", "HUMAN HERPESVIRUS 8, susceptibility to", "human herpesvirus 8, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "human herpesvirus 8, susceptibility to", "shortest_name_length": 5}
{"curie": "UMLS:C4528592", "names": ["Stage IV Breast Cancer", "Prognostic Stage IV Breast Cancer AJCC v8", "Prognostic Stage IV Breast Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prognostic Stage IV Breast Cancer AJCC v8", "shortest_name_length": 22}
{"curie": "MONDO:0004100", "names": ["combined small and large cell lung cancer", "small cell and squamous cell lung carcinoma", "Small Cell and Squamous Cell Lung Carcinoma", "small cell and squamous cell carcinoma of lung", "Small Cell and Squamous Cell Carcinoma of Lung", "small cell and large cell carcinoma of the lung", "lung mixed small cell and squamous cell carcinoma", "small cell and squamous cell carcinoma of the lung", "Small Cell and Squamous Cell Carcinoma of the Lung", "combined small cell and squamous cell lung carcinoma", "Mixed Small Cell and Squamous Cell Carcinoma of Lung", "mixed small cell and squamous cell carcinoma of lung", "Combined Lung Small Cell and Squamous Cell Carcinoma", "Combined Small Cell and Squamous Cell Lung Carcinoma", "mixed small cell and squamous cell carcinoma of the lung", "Mixed Small Cell and Squamous Cell Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung mixed small cell and squamous cell carcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0008149", "names": ["osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures", "Osteogenesis Imperfecta with Opalescent Teeth, Blue Sclerae and Wormian Bones, but Without Fractures", "osteogenesis imperfecta with opalescent teeth, blue sclerae and WORMIAN bones, but without fractures", "OSTEOGENESIS IMPERFECTA WITH OPALESCENT TEETH, BLUE SCLERAE AND WORMIAN BONES, BUT WITHOUT FRACTURES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures", "shortest_name_length": 99}
{"curie": "MONDO:0006969", "names": ["Sialitis", "sialitis", "Sialitides", "SIALADENITIS", "Sialadenitis", "sialadenitis", "Sialoadenitis", "SIALOADENITIS", "sialoadenitis", "Sialadenitides", "Sialoadenitides", "Sialoadenitis NOS", "Sialadenitis, NOS", "Sialoadenitis, NOS", "Chronic Sialadenitis", "Sialadenitis, Chronic", "Chronic Sialadenitides", "Salivary Gland Adenitis", "Sialadenitides, Chronic", "Sialoadenitis (disorder)", "Adenitis, Salivary Gland", "salivary gland; adenitis", "adenitis; salivary gland", "adenitis, salivary gland", "Salivary Gland Adenitides", "sialoadenitis (diagnosis)", "Sialoadenitis, unspecified", "Adenitides, Salivary Gland", "Salivary Gland Inflammation", "salivary gland inflammation", "Salivary gland inflammation", "SALIVARY GLAND INFLAMMATION", "salivary glands inflammation", "salivary gland; inflammation", "Inflammation, Salivary Gland", "Salivary Gland Inflammations", "Inflammations, Salivary Gland", "salivary glands inflammation (diagnosis)", "saliva-secreting gland lymphadenitis (disease)", "lymphadenitis (disease) of saliva-secreting gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sialadenitis", "shortest_name_length": 8}
{"curie": "UMLS:C1720795", "names": ["Acute Bacterial Prostatitis", "acute bacterial prostatitis", "Bacterial Prostatitis, Acute", "Acute Bacterial Prostatitides", "Bacterial Prostatitides, Acute", "acute bacterial prostatitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Bacterial Prostatitis", "shortest_name_length": 27}
{"curie": "MONDO:0016071", "names": ["Puretic syndrome", "Molluscum fibrosum", "mesenchymal dysplasia", "Infantile Systemic Hyalinosis", "Juvenile Hyaline Fibromatosis", "juvenile hyaline fibromatosis", "Hyaline Fibromatosis Syndrome", "Murray-Puretic-Drescher syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile hyaline fibromatosis", "shortest_name_length": 16}
{"curie": "UMLS:C1444077", "names": ["bone abscess", "Bone abscess", "bone; abscess", "abscess; bone", "Abscess;bone(s)", "Bone abscess (disorder)", "bone abscess (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone abscess", "shortest_name_length": 12}
{"curie": "MONDO:0008434", "names": ["SMS", "SMCR", "monosomy 17p", "17p- syndrome", "del(17p) syndrome", "partial monosomy 17p", "17p deletion syndrome", "deletion 17p syndrome", "SMITH-Magenis syndrome", "Smith Magenis Syndrome", "magenis syndrome smith", "Smith-Magenis Syndrome", "magenis smith syndrome", "Smith-Magenis syndrome", "Smith Magenis syndrome", "SMITH-MAGENIS SYNDROME", "smith-magenis syndrome", "smith magenis syndrome", "Syndrome, Smith-Magenis", "chromosome 17p monosomy", "Smith-Magenis syndrome (SMS)", "17p11.2 microdeletion syndrome", "Smith-Magenis chromosome region", "chromosome 17p deletion syndrome", "Smith-Magenis syndrome (disorder)", "Smith-Magenis syndrome (diagnosis)", "Chromosome 17p11.2 Deletion Syndrome", "chromosome 17p11.2 deletion syndrome", "CHROMOSOME 17p11.2 DELETION SYNDROME", "chromosome 17P11.2 deletion syndrome", "Smith-Magenis syndrome, Isolated cases", "SMITH-MAGENIS SYNDROME CHROMOSOME REGION", "Smith-Magenis syndrome chromosome region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Smith-Magenis syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0011434", "names": ["PSORS5", "psoriasis 5", "PSORIASIS SUSCEPTIBILITY 5", "psoriasis susceptibility 5", "psoriasis 5, susceptibility to", "PSORIASIS 5, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "psoriasis 5, susceptibility to", "shortest_name_length": 6}
{"curie": "MONDO:0006361", "names": ["penile induration", "Penile Induration", "penis fibromatosis", "Peyronie's Disease", "Peyronie's disease", "Penile Fibromatosis", "penile fibromatosis", "Peyronie's fibromatosis", "Peyronie's Fibromatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "penile fibromatosis", "shortest_name_length": 17}
{"curie": "MONDO:0032710", "names": ["DEE72", "EIEE72", "early infantile epileptic encephalopathy 72", "developmental and epileptic encephalopathy 72", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 72", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 72", "epileptic encephalopathy, early infantile, 72", "developmental and epileptic encephalopathy, 72"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 72", "shortest_name_length": 5}
{"curie": "UMLS:C0349611", "names": ["Brain Hamartoma", "Hamartoma of brain", "Hamartoma of brain (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hamartoma of brain", "shortest_name_length": 15}
{"curie": "UMLS:C3665770", "names": ["Acquired lipoatrophic diabetes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired lipoatrophic diabetes", "shortest_name_length": 30}
{"curie": "MONDO:0030458", "names": ["CMT2HH", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2HH", "Charcot-Marie-Tooth disease, axonal, Type 2HH", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2HH"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease, axonal, Type 2HH", "shortest_name_length": 6}
{"curie": "UMLS:C5237353", "names": ["CIC-DUX4 Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CIC-DUX4 Sarcoma", "shortest_name_length": 16}
{"curie": "UMLS:C5554894", "names": ["Epithelioid Schwannoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epithelioid Schwannoma", "shortest_name_length": 22}
{"curie": "UMLS:C1332042", "names": ["AIDS-Related Diffuse Large B-cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Diffuse Large B-cell Lymphoma", "shortest_name_length": 42}
{"curie": "UMLS:C4682562", "names": ["Stage IIIC Uterine Corpus Leiomyosarcoma", "Stage IIIC Uterine Corpus Leiomyosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Uterine Corpus Leiomyosarcoma AJCC v8", "shortest_name_length": 40}
{"curie": "MONDO:0017294", "names": ["glycerol kinase deficiency, infantile form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycerol kinase deficiency, infantile form", "shortest_name_length": 42}
{"curie": "UMLS:C5420650", "names": ["Recurrent Supratentorial Glioblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Supratentorial Glioblastoma", "shortest_name_length": 37}
{"curie": "UMLS:C0860210", "names": ["Granulomatous liver disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Granulomatous liver disease", "shortest_name_length": 27}
{"curie": "MONDO:0000909", "names": ["BARTS4B", "Bartter disease type 4B", "Bartter disease type 4b", "Bartter Syndrome, Type 4b", "Bartter syndrome, type 4B", "BARTTER SYNDROME, TYPE 4B", "Bartter syndrome, type 4b, digenic", "Bartter Syndrome, Infantile, with Sensorineural Deafness", "Bartter syndrome, infantile, with sensorineural deafness", "neonatal Bartter syndrome type 4B with sensorineural deafness", "BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS", "Bartter syndrome, type 4B, neonatal, with sensorineural deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bartter disease type 4B", "shortest_name_length": 7}
{"curie": "MONDO:0003573", "names": ["Pleomorphic Carcinoma", "pleomorphic carcinoma", "Pleomorphic carcinoma", "pleomorphic carcinoma (diagnosis)", "Pleomorphic carcinoma (morphologic abnormality)", "pleomorphic carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pleomorphic carcinoma", "shortest_name_length": 21}
{"curie": "MONDO:0000674", "names": ["mirror agnosia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mirror agnosia", "shortest_name_length": 14}
{"curie": "UMLS:C0855176", "names": ["Stage I Bladder Adenocarcinoma", "Bladder adenocarcinoma stage I", "Bladder Adenocarcinoma Stage I", "Stage I Bladder Adenocarcinoma AJCC v7", "Stage I Bladder Adenocarcinoma AJCC v6", "Stage I Bladder Adenocarcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder adenocarcinoma stage I", "shortest_name_length": 30}
{"curie": "UMLS:C0152010", "names": ["Withdrawal bleed", "withdrawal bleed", "bleeding withdrawal", "WITHDRAWAL BLEEDING", "Withdrawal bleeding", "withdrawal bleeding", "Withdrawal bleeding (finding)", "bleed contraceptives withdrawal", "Contraceptive withdrawal bleeding", "CONTRACEPTIVE WITHDRAWAL BLEEDING", "BLEEDING WITHDRAWAL (CONTRACEPTIVE)", "Bleeding withdrawal (contraceptive)", "Hemorrhage withdrawal (contraceptive)", "HEMORRHAGE WITHDRAWAL (CONTRACEPTIVE)", "Haemorrhage withdrawal (contraceptive)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Withdrawal bleeding", "shortest_name_length": 16}
{"curie": "UMLS:C1334213", "names": ["Intermediate Fibrohistiocytic Tumor", "Intermediate Fibrohistiocytic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intermediate Fibrohistiocytic Neoplasm", "shortest_name_length": 35}
{"curie": "UMLS:C1260913", "names": ["Pneumococcal arthritis or polyarthritis", "Pneumococcal arthritis and polyarthritis", "Arthritis or Polyarthritis due to Pneumococcus", "Arthritis or polyarthritis due to pneumococcus", "Pneumococcal arthritis and polyarthritis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pneumococcal arthritis and polyarthritis", "shortest_name_length": 39}
{"curie": "MONDO:0019423", "names": ["X-linked intellectual disability Stoll type", "X-linked intellectual disability, Stoll type", "X-linked intellectual disability Stoll type (disorder)", "X-linked intellectual disability Stoll type (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability, Stoll type", "shortest_name_length": 43}
{"curie": "UMLS:C5205872", "names": ["LUNG RADIATION INJURY", "Lung Radiation Injury", "Pulmonary Radiation Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Radiation Injury", "shortest_name_length": 21}
{"curie": "MONDO:0002076", "names": ["pneumothorax", "PNEUMOTHORAX", "Pneumothorax", "Collapsed lung", "Pneumothorax NOS", "Pneumothorax, NOS", "Air in pleural space", "pneumothorax disorder", "pneumothorax (disease)", "Pneumothorax (disorder)", "pneumothorax (diagnosis)", "Pneumothorax, unspecified", "Other spontaneous pneumothorax", "free air in the chest outside the lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pneumothorax", "shortest_name_length": 12}
{"curie": "UMLS:C0948856", "names": ["Orgasmic sensation decreased"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Orgasmic sensation decreased", "shortest_name_length": 28}
{"curie": "UMLS:C5556737", "names": ["HPV-Related Vaginal Adenocarcinoma", "HPV-Associated Vaginal Adenocarcinoma", "Human Papillomavirus-Related Vaginal Adenocarcinoma", "Human Papillomavirus-Associated Vaginal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Human Papillomavirus-Related Vaginal Adenocarcinoma", "shortest_name_length": 34}
{"curie": "UMLS:C5447388", "names": ["YARSopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "YARSopathy", "shortest_name_length": 10}
{"curie": "MONDO:0024935", "names": ["foot rot", "Foot rot", "Foot Rot", "rot, foot", "Rot, Foot", "foot Rots", "Foot Rots", "Rots, Foot", "Rots, foot", "Bovine foot rot", "Foul-in-the-foot", "Infectious pododermatitis", "Interdigital necrobacillosis", "Infectitious pododermatitis of the hoof", "Contagious pododermatitis of hoof (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "foot rot", "shortest_name_length": 8}
{"curie": "MONDO:0011841", "names": ["BBGD", "THMD2", "BTBGD", "Thiamine transporter-2 deficiency", "Thiamine-responsive encephalopathy", "thiamine-responsive encephalopathy", "ENCEPHALOPATHY, THIAMINE-RESPONSIVE", "encephalopathy, thiamine-responsive", "Biotin-responsive basal ganglia disease", "biotin-responsive basal ganglia disease", "BASAL GANGLIA DISEASE, BIOTIN-RESPONSIVE", "Basal ganglia disease, biotin-responsive", "basal ganglia disease, biotin-responsive", "Thiamine metabolism dysfunction syndrome 2", "Thiamine-responsive encephalopathy (disorder)", "Biotin-thiamine-responsive basal ganglia disease", "biotin-thiamine-responsive basal ganglia disease", "Biotin-thiamine-responsive basal ganglia disease (disorder)", "THIAMINE METABOLISM DYSFUNCTION SYNDROME 2 (BIOTIN- OR THIAMINE-RESPONSIVE TYPE)", "thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive type)", "thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "biotin-responsive basal ganglia disease", "shortest_name_length": 4}
{"curie": "MONDO:0008368", "names": ["AD dRTA", "RTA, classic type", "RTA, gradient type", "renal tubular acidosis 1", "distal renal tubular acidosis 1", "RTA, distal type, autosomal dominant", "autosomal dominant distal renal tubular acidosis", "renal tubular acidosis, distal, autosomal dominant", "autosomal dominant distal renal tubular acidosis (disease)", "distal renal tubular acidosis (disease), autosomal dominant", "autosomal dominant SLC4A1-associated distal renal tubular acidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant distal renal tubular acidosis", "shortest_name_length": 7}
{"curie": "MONDO:0024543", "names": ["BCS1", "EDS6B, FORMERLY", "Brittle cornea syndrome", "Ehlers-Danlos syndrome 6B", "Brittle cornea syndrome 1", "brittle cornea syndrome 1", "BRITTLE CORNEA SYNDROME 1", "ZNF469 brittle cornea syndrome", "Ehlers-Danlos syndrome type 6B", "Ehlers-Danlos syndrome, type Vib", "Ehlers-Danlos Syndrome, Type VIB", "Brittle cornea syndrome (disorder)", "dysgenesis Mesodermalis corneae Et sclerae", "EHLERS-DANLOS SYNDROME, TYPE VIB, FORMERLY", "Dysgenesis Mesodermalis Corneae et Sclerae", "Ehlers-Danlos syndrome, type Vib, formerly", "DYSGENESIS MESODERMALIS CORNEAE ET SCLERAE", "Fragilitas oculi with joint hyperextensibility", "Fragilitas oculi with Joint hyperextensibility", "FRAGILITAS OCULI WITH JOINT HYPEREXTENSIBILITY", "brittle cornea syndrome caused by mutation in ZNF469", "corneal fragility, keratoglobus, blue sclerae, Joint hyperextensibility", "CORNEAL FRAGILITY, KERATOGLOBUS, BLUE SCLERAE, JOINT HYPEREXTENSIBILITY", "Corneal fragility, keratoglobus, blue sclerae, joint hyperextensibility"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brittle cornea syndrome 1", "shortest_name_length": 4}
{"curie": "MONDO:0100509", "names": ["retinitis pigmentosa 80", "IFT140-related recessive ciliopathy", "short-rib thoracic dysplasia 9 with or without polydactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IFT140-related recessive ciliopathy", "shortest_name_length": 23}
{"curie": "MONDO:0011450", "names": ["HBOC1", "BROVCA1", "BREAST CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1", "breast cancer, familial, susceptibility to, 1", "OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1", "ovarian cancer, familial, susceptibility to, 1", "BRCA1 hereditary breast ovarian cancer syndrome", "breast-ovarian cancer, familial, 1, multifactorial", "susceptibility to familial breast-ovarian cancer 1", "BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1", "breast-ovarian cancer, familial, susceptibility to, 1", "breast-ovarian cancer, familial, susceptibility to, type 1", "hereditary breast ovarian cancer syndrome caused by mutation in BRCA1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast-ovarian cancer, familial, susceptibility to, 1", "shortest_name_length": 5}
{"curie": "UMLS:C0752100", "names": ["Autosomal Recessive Parkinsonism", "Parkinsonism, Autosomal Recessive", "Recessive Parkinsonism, Autosomal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Autosomal Recessive Parkinsonism", "shortest_name_length": 32}
{"curie": "MONDO:0002665", "names": ["extrahepatic bile duct adenocarcinoma", "Extrahepatic Bile Duct Adenocarcinoma", "adenocarcinoma of extrahepatic bile duct", "Adenocarcinoma of Extrahepatic Bile Duct", "adenocarcinoma of the extrahepatic bile duct", "Adenocarcinoma of the Extrahepatic Bile Duct", "extrahepatic bile duct, adenocarcinoma of the", "extrahepatic bile duct cancer, adenocarcinoma", "bile duct cancer, extrahepatic, adenocarcinoma", "adenocarcinoma of extrahepatic bile duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extrahepatic bile duct adenocarcinoma", "shortest_name_length": 37}
{"curie": "UMLS:C5555931", "names": ["Esophageal Carcinoma Cuniculatum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Carcinoma Cuniculatum", "shortest_name_length": 32}
{"curie": "MONDO:0010972", "names": ["Waaler-Aarskog syndrome", "Waaler Aarskog syndrome", "Ferlini Ragno Calzolari syndrome", "Ferlini-Ragno-Calzolari syndrome", "hydrocephalus, skeletal anomalies, and mental disturbance", "hydrocephalus, Sprengel anomaly, and costovertebral dysplasia", "HYDROCEPHALUS, SPRENGEL ANOMALY, AND COSTOVERTEBRAL DYSPLASIA", "hydrocephalus, costovertebral dysplasia, and Sprengel anomaly", "hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome", "Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome", "Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome", "Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0022653", "names": ["cardiomyopathy due to anthracyclines"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiomyopathy due to anthracyclines", "shortest_name_length": 36}
{"curie": "MONDO:0006212", "names": ["flat urothelial hyperplasia", "Flat Urothelial Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "flat urothelial hyperplasia", "shortest_name_length": 27}
{"curie": "UMLS:C0280369", "names": ["oropharynx lymphoepithelioma, stage I", "Oropharyngeal lymphepithelioma stage I", "Oropharyngeal lymphoepithelioma stage I", "Stage I Oropharyngeal Lymphoepithelioma", "oropharyngeal lymphoepithelioma, stage I", "stage I lymphoepithelioma of the oropharynx", "lymphoepithelioma of the oropharynx, stage I", "Stage I Oropharyngeal Lymphoepithelioma AJCC v7", "Stage I Oropharyngeal Lymphoepithelioma AJCC v6", "Stage I Oropharyngeal Undifferentiated Carcinoma", "Stage I Undifferentiated Oropharyngeal Throat Cancer", "Stage I Oropharyngeal Undifferentiated Carcinoma AJCC v7", "Stage I Oropharyngeal Undifferentiated Carcinoma AJCC v6", "Stage I Oropharyngeal Undifferentiated Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oropharyngeal lymphoepithelioma stage I", "shortest_name_length": 37}
{"curie": "MONDO:0004811", "names": ["Simple chronic conjunctivitis", "simple chronic conjunctivitis", "chronic simple conjunctivitis", "Simple chronic conjunctivitis (disorder)", "chronic simple conjunctivitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "simple chronic conjunctivitis", "shortest_name_length": 29}
{"curie": "UMLS:C0340481", "names": ["Congenital His bundle tachycardia", "Congenital His Bundle Tachycardia", "Congenital Bundle of His Tachycardia", "Junctional Ectopic Tachycardia, Congenital", "Congenital His bundle tachycardia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital His bundle tachycardia", "shortest_name_length": 33}
{"curie": "MONDO:0013616", "names": ["PPNAD3", "Cushing syndrome, adrenal, due to PPNAD3", "CUSHING SYNDROME, ADRENAL, DUE TO PPNAD3", "pigmented nodular adrenocortical disease, primary, 3", "PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 3", "PDE8B primary pigmented nodular adrenocortical disease", "pigmented nodular adrenocortical disease, primary, type 3", "primary pigmented nodular adrenocortical disease caused by mutation in PDE8B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pigmented nodular adrenocortical disease, primary, 3", "shortest_name_length": 6}
{"curie": "MONDO:0000380", "names": ["paranasal sinus cancer", "Accessory Sinus Cancer", "accessory sinus cancer", "Paranasal sinus cancer", "sinus paranasal cancer", "Paranasal Sinus Cancer", "Paranasal Sinus Cancers", "Cancer, Paranasal Sinus", "Cancers, Paranasal Sinus", "Accessory Sinus Carcinoma", "Paranasal Sinus Carcinoma", "accessory sinus carcinoma", "paranasal sinus carcinoma", "cancer of paranasal sinus", "Cancer of Paranasal Sinus", "Paranasal sinus cancer NOS", "Carcinoma of Paranasal Sinus", "Carcinoma of Accessory Sinus", "carcinoma of accessory sinus", "carcinoma of paranasal sinus", "Cancer of the paranasal sinus", "Paranasal Sinus Adenocarcinoma", "Accessory Sinus Adenocarcinoma", "paranasal sinus adenocarcinoma", "Carcinoma of the Paranasal Sinus", "carcinoma of the paranasal sinus", "Carcinoma of the Accessory Sinus", "carcinoma of the accessory sinus", "Adenocarcinoma of Accessory Sinus", "Adenocarcinoma of accessory sinus", "Adenocarcinoma of Paranasal Sinus", "adenocarcinoma of accessory sinus", "malignant paranasal sinus neoplasm", "Adenocarcinoma of the Paranasal Sinus", "malignant neoplasm of paranasal sinus", "Adenocarcinoma of the Accessory Sinus", "paranasal sinus squamous cell carcinoma", "paranasal sinus mucoepidermoid carcinoma", "carcinoma of accessory sinus (diagnosis)", "paranasal sinus adenoid cystic carcinoma", "squamous cell carcinoma of paranasal sinus", "Epidermoid carcinoma of the paranasal sinus", "epidermoid carcinoma of the paranasal sinus", "adenoid cystic carcinoma of paranasal sinus", "mucoepidermoid carcinoma of accessory sinus", "Mucoepidermoid carcinoma of Accessory sinus", "adenoid cystic carcinoma of accessory sinus", "adenoid cystic carcinoma of Accessory sinus", "Adenocarcinoma of accessory sinus (disorder)", "adenocarcinoma of accessory sinus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paranasal sinus carcinoma", "shortest_name_length": 22}
{"curie": "MONDO:0014605", "names": ["MRD36", "autosomal dominant mental retardation 36", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 36", "mental retardation, autosomal dominant 36", "autosomal dominant intellectual disability 36", "intellectual disability, autosomal dominant 36", "mental retardation, autosomal dominant type 36", "intellectual disability, autosomal dominant type 36", "autosomal dominant intellectual developmental disorder 36", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 36", "autosomal dominant non-syndromic intellectual disability 36", "microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome", "Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome", "Microcephaly, corpus callosum hypoplasia, intellectual disability, facial dysmorphism syndrome", "Microcephaly, corpus callosum hypoplasia, intellectual disability, facial dysmorphism syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0342548", "names": ["early menarche", "Early menarche", "precocious menses", "premature menarche", "Premature Menarche", "Premature menarche", "Precocious menstruation", "precocious menstruation", "menstruation; precocious", "precocious; menstruation", "Early menarche (finding)", "precocious menses (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Early menarche", "shortest_name_length": 14}
{"curie": "MONDO:0015843", "names": ["uterine hypoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine hypoplasia", "shortest_name_length": 18}
{"curie": "MONDO:0019253", "names": ["metabolic disease involving other neurotransmitter deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metabolic disease involving other neurotransmitter deficiency", "shortest_name_length": 61}
{"curie": "MONDO:0019426", "names": ["X-linked intellectual disability - corpus callosum agenesis - spastic quadriparesis", "X-linked intellectual disability-corpus callosum agenesis-spastic quadriparesis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability-corpus callosum agenesis-spastic quadriparesis syndrome", "shortest_name_length": 83}
{"curie": "UMLS:C2717759", "names": ["Degenerative Intervertebral Disc", "Degenerative Intervertebral Disk", "Disk, Degenerative Intervertebral", "Degenerative Intervertebral Discs", "Intervertebral Disc, Degenerative", "Disc, Degenerative Intervertebral", "Intervertebral Disk, Degenerative", "Degenerative Intervertebral Disks"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Degenerative Intervertebral Discs", "shortest_name_length": 32}
{"curie": "UMLS:C5206339", "names": ["Locally Advanced Unresectable Gastroesophageal Junction Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Unresectable Gastroesophageal Junction Adenocarcinoma", "shortest_name_length": 70}
{"curie": "MONDO:0007106", "names": ["ASDP", "anal sphincter dysplasia", "ANAL SPHINCTER DYSPLASIA", "Anal sphincter dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anal sphincter dysplasia", "shortest_name_length": 4}
{"curie": "MONDO:0017907", "names": ["conjunctiva lymphoma", "lymphoma of conjunctiva", "Primary lymphoma of conjunctiva", "eye malignant lymphoma conjunctiva", "primary lymphoid conjunctival tumor", "Primary lymphoma of the conjunctiva", "primary lymphoma of the conjunctiva", "Primary lymphoid conjunctival tumor", "Primary lymphoid conjunctival tumour", "Primary lymphoma of conjunctiva (disorder)", "Primary lymphoma of conjunctiva (diagnosis)", "conjunctiva primary organ-specific lymphoma", "primary organ-specific lymphoma of conjunctiva"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary lymphoma of the conjunctiva", "shortest_name_length": 20}
{"curie": "MONDO:0019362", "names": ["typhus", "jail fever", "Jail Fever", "FEVER, WAR", "DERMOTYPHO", "TABARDILLO", "CAMP FEVER", "tabardillo", "Tabardillo", "fleckfieber", "FEVER, JAIL", "Hildenbrand", "Fleckfieber", "Fever, Jail", "FEVER, CAMP", "FLECKFIEBER", "lice; typhus", "epidemic typhus", "Epidemic typhus", "sylvatic typhus", "Epidemic Typhus", "European typhus", "epidemic; typhus", "Classical Typhus", "typhus; epidemic", "lice; tabardillo", "TYPHUS, EPIDEMIC", "Classical typhus", "Typhus, Epidemic", "classical; typhus", "typhus; classical", "Louse Borne Typhus", "louse-borne typhus", "Louse-borne typhus", "TIFUS EXANTEMATICO", "Louse-Borne Typhus", "Louse-borne Typhus", "exanthematic typhus", "Exanthematic typhus", "Tifus exanthematico", "typhus; louse-borne", "Typhus, louse-borne", "Typhus, Louse-Borne", "exanthematic; typhus", "typhus; exanthematic", "Epidemic Typhus fever", "TYPHUS EXANTHEMATIQUE", "Epidemic Typhus Fever", "epidemic typhus fever", "Classical Typhus fever", "tabardillo; louse-borne", "Exanthematic Typhus NOS", "Exanthematic typhus, NOS", "louse-borne typhus fever", "Classical typhus (fever)", "Louse-borne typhus fever", "Louse-borne Typhus fever", "Epidemic Louse-Borne Typhus", "Epidemic Louse-borne typhus", "Louse-borne epidemic typhus", "epidemic louse-borne typhus", "Epidemic louse-borne typhus", "Typhus, Epidemic Louse Borne", "Louse-Borne Typhus, Epidemic", "Typhus, Epidemic Louse-Borne", "Exanthematic Typhus fever NOS", "Louse-borne typhus (disorder)", "Louse-borne (epidemic) typhus", "typhus; Rickettsia prowazekii", "Epidemic (louse-borne) typhus", "Rickettsia; prowazekii, typhus", "louse-borne typhus (diagnosis)", "Rickettsia prowazekii Infection", "Rickettsia prowazekii infection", "Rickettsia prowazekii Infections", "Infection, Rickettsia prowazekii", "epidemic (louse borne) typhus fever", "Typhus due to Rickettsia prowazekii", "rickettsiosis; Rickettsia prowazekii", "prowazekii; Rickettsia prowazekii, typhus", "Epidemic louse-borne typhus fever due to Rickettsia prowazekii"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidemic louse-borne typhus", "shortest_name_length": 6}
{"curie": "UMLS:C1332286", "names": ["Malignant Intraspinal Meningioma", "Anaplastic Intraspinal Meningioma", "Anaplastic (Malignant) Intraspinal Meningioma", "Malignant Spinal Canal and Spinal Cord Meningioma", "Malignant Meningioma of Spinal Canal and Spinal Cord", "Malignant Meningioma of the Spinal Canal and Spinal Cord"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anaplastic (Malignant) Intraspinal Meningioma", "shortest_name_length": 32}
{"curie": "MONDO:0002122", "names": ["NEURITIS", "neuritis", "Neuritis", "Neuritides", "neuritides", "Neuritis NOS", "Neuritis, NOS", "nerve inflammation", "Neuritis;peripheral", "Peripheral Neuritis", "peripheral neuritis", "neuritis peripheral", "NEURITIS PERIPHERAL", "Peripheral neuritis", "Neuritis peripheral", "PERIPHERAL NEURITIS", "Neuritis, Peripheral", "neuritis; peripheral", "peripheral; neuritis", "neuritis (diagnosis)", "Peripheral Neuritides", "Neuritides, Peripheral", "Peripheral neuritis NOS", "Inflammatory neuropathy", "inflammatory neuropathy", "Peripheral neuritis, NOS", "inflammatory neuropathies", "Inflammatory neuropathy, NOS", "Peripheral neuritis (disorder)", "Inflammatory neuropathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuritis", "shortest_name_length": 8}
{"curie": "UMLS:C1696110", "names": ["Vessel puncture site hematoma", "Vessel puncture site haematoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vessel puncture site hematoma", "shortest_name_length": 29}
{"curie": "MONDO:0020219", "names": ["corneogoniodysgenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneogoniodysgenesis", "shortest_name_length": 21}
{"curie": "MONDO:0054698", "names": ["CANDLE", "PRAAS1", "JMP syndrome", "CANDLE syndrome", "Nakajo-Nishimura syndrome", "Proteasome-Associated Autoinflammatory Syndrome 1", "proteasome-associated autoinflammatory syndrome 1", "PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1", "autoinflammation, lipodystrophy, and dermatosis syndrome", "proteasome-associated autoinflammatory syndrome 1, digenic", "PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1, DIGENIC", "proteasome-associated autoinflammatory syndrome 1 and digenic forms", "Chronic Atypical Neutrophilic Dermatosis with Lipodystrophy and Elevated Temperature Syndrome", "chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature syndrome", "CHRONIC ATYPICAL NEUTROPHILIC DERMATOSIS WITH LIPODYSTROPHY AND ELEVATED TEMPERATURE SYNDROME", "Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature syndrome", "joint contractures, muscular atrophy, microcytic Anemia, and panniculitis-induced lipodystrophy", "Chronic Atypical Neutrophilic Dermatosis with Lipodystrophy and Elevated Temperature (CANDLE) Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "proteasome-associated autoinflammatory syndrome 1", "shortest_name_length": 6}
{"curie": "UMLS:C4761201", "names": ["Pleomorphic Leiomyosarcoma", "Pleomorphic leiomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pleomorphic leiomyosarcoma", "shortest_name_length": 26}
{"curie": "MONDO:0024649", "names": ["optic tract astrocytoma", "visual pathway astrocytoma", "Visual Pathway Astrocytoma", "optic tract astrocytoma (excluding glioblastoma)", "astrocytoma (excluding glioblastoma) of optic tract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "optic tract astrocytoma", "shortest_name_length": 23}
{"curie": "MONDO:0004338", "names": ["retinal cell cancer", "cancer of retinal cell", "malignant retinal cell neoplasm", "malignant neoplasm of retinal cell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal cell cancer", "shortest_name_length": 19}
{"curie": "MONDO:0032733", "names": ["GDPAG", "GLOBAL DEVELOPMENTAL DELAY, PROGRESSIVE ATAXIA, AND ELEVATED GLUTAMINE", "global developmental delay, progressive ataxia, and elevated glutamine", "Glutaminase Deficiency With Impaired Intellectual Development and Progressive Ataxia", "GLUTAMINASE DEFICIENCY WITH IMPAIRED INTELLECTUAL DEVELOPMENT AND PROGRESSIVE ATAXIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "global developmental delay, progressive ataxia, and elevated glutamine", "shortest_name_length": 5}
{"curie": "MONDO:0018375", "names": ["traumatic AVN", "traumatic avascular necrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "traumatic avascular necrosis", "shortest_name_length": 13}
{"curie": "MONDO:0007593", "names": ["Facial tic", "facial tic", "Tic;facial", "Facial tics", "facial tics", "facial spasm", "Facial spasm", "Mimic spasms", "FACIAL SPASM", "spasm; facial", "facial; spasm", "facial spasms", "facial twitch", "Facial spasms", "Facial twitching", "Twitching facial", "facial twitching", "twitching facial", "Twitching of face", "Facial spasm, NOS", "facial muscle spasm", "Facial tic disorder", "facial tic disorder", "FACIAL MUSCLE SPASM", "facial muscle spasms", "facial muscles spasm", "Muscle spasm of face", "Facial spasm (finding)", "facial muscle twitching", "Spasms of facial muscles", "Jerking of facial muscles", "Cramping of facial muscles", "Facial twitching (finding)", "Myoclonus of facial muscles", "Twitching of facial muscles", "facial muscle spasm (symptom)", "Facial tic disorder (disorder)", "facial tic disorder (diagnosis)", "Involuntary facial muscle spasms", "facial muscle twitching (symptom)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "facial spasm", "shortest_name_length": 10}
{"curie": "MONDO:0012348", "names": ["DPED", "MODY8", "MODY type 8", "diabetes mellitus MODY type 8", "diabetes and pancreatic exocrine", "maturity-onset diabetes of the young type 8", "type 8 maturity-onset diabetes of the young", "Maturity-onset diabetes of the young, type 8", "diabetes and pancreatic exocrine dysfunction", "Diabetes and Pancreatic Exocrine Dysfunction", "maturity-onset diabetes of the young, type 8", "DIABETES AND PANCREATIC EXOCRINE DYSFUNCTION", "maturity-onset diabetes of the young - type 8", "maturity-onset diabetes of the young, type VIII", "diabetes-pancreatic exocrine dysfunction syndrome", "DIABETES-PANCREATIC EXOCRINE DYSFUNCTION SYNDROME", "Diabetes-Pancreatic Exocrine Dysfunction Syndrome", "Diabetes-pancreatic exocrine dysfunction syndrome", "CEL maturity-onset diabetes of the young (disease)", "Maturity-onset diabetes of the young, type 8 (disorder)", "maturity-onset diabetes of the young - type 8 (diagnosis)", "maturity-onset diabetes of the young type 8 with exocrine dysfunction", "Maturity-Onset Diabetes of the Young, Type 8, with Exocrine Dysfunction", "MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 8, WITH EXOCRINE DYSFUNCTION", "maturity-onset diabetes of the young, type 8, with exocrine dysfunction", "maturity-onset diabetes of the young (disease) caused by mutation in CEL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maturity-onset diabetes of the young type 8", "shortest_name_length": 4}
{"curie": "UMLS:C5557400", "names": ["Vulvar Distal-Type Epithelioid Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Distal-Type Epithelioid Sarcoma", "shortest_name_length": 38}
{"curie": "MONDO:0000261", "names": ["Adenoiditis", "adenoiditis", "Adenoiditis, NOS", "chronic adenoiditis", "Chronic adenoiditis", "pharyngeal tonsilitis", "Adenoiditis (disorder)", "adenoiditis (diagnosis)", "inflammation of adenoids", "Chronic adenoiditis (disorder)", "pharyngeal tonsil inflammation", "chronic adenoiditis (diagnosis)", "inflammation of pharyngeal tonsil", "inflammation of adenoids (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenoiditis", "shortest_name_length": 11}
{"curie": "MONDO:0014937", "names": ["AN2", "ANIRIDIA 2", "aniridia 2", "Aniridia type 2", "aniridia 2; AN2", "aniridia type 2", "Aniridia, type 2", "Aniridia type 2 (disorder)", "Aniridia type 2 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aniridia 2", "shortest_name_length": 3}
{"curie": "MONDO:0016543", "names": ["hyperphenylalaninemia", "Hyperphenylalaninemia", "Hyperphenylalaninaemia", "hyperphenylalaninaemia", "hyperphenylalaninaemias", "Hyperphenylalaninemia, NOS", "Hyperphenylalaninemia (disorder)", "hyperphenylalaninemia (diagnosis)", "non-phenylketonuric hyperphenylalaninemia", "hyperphenylalaninemia due to BH4 deficiency", "hyperphenylalaninemia due to tetrahydrobiopterin deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperphenylalaninemia due to tetrahydrobiopterin deficiency", "shortest_name_length": 21}
{"curie": "UMLS:C4553412", "names": ["IIA2", "Stage IIA2 Cervical Cancer", "Stage IIA2 Cervical Cancer AJCC v8", "Stage IIA2 Cervical Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA2 Cervical Cancer AJCC v8", "shortest_name_length": 4}
{"curie": "MONDO:0800100", "names": ["RDH12-related dominant retinopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "RDH12-related dominant retinopathy", "shortest_name_length": 34}
{"curie": "UMLS:C1336373", "names": ["Stage IVB Larynx Carcinoma", "stage IVB laryngeal cancer", "Stage IVB Laryngeal Cancer", "Laryngeal Cancer Stage IVB", "Stage IVB Carcinoma of Larynx", "Stage IVB Laryngeal Carcinoma", "Stage IVB Laryngeal Throat Cancer", "Stage IVB Carcinoma of the Larynx", "Stage IVB Laryngeal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Laryngeal Cancer AJCC v7", "shortest_name_length": 26}
{"curie": "MONDO:0007805", "names": ["HTSS", "Htss", "hypt2", "Htss1", "HYPT2", "Hypt2", "HTSS1", "HYPOTRICHOSIS 2", "hypotrichosis 2", "CDSN hypotrichosis", "hypotrichosis type 2", "Spanish type hypotrichosis", "hypotrichosis, Spanish type", "Hypotrichosis, Spanish Type", "HYPOTRICHOSIS, SPANISH TYPE", "Hypotrichosis Simplex of Scalp", "Hypotrichosis simplex of scalp", "Hypotrichosis simplex of the scalp", "hypotrichosis simplex of the scalp 1", "HYPOTRICHOSIS SIMPLEX OF THE SCALP 1", "hypotrichosis caused by mutation in CDSN", "Hereditary hypotrichosis simplex of scalp", "Hereditary hypotrichosis simplex of the scalp", "Hereditary hypotrichosis simplex of scalp (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotrichosis 2", "shortest_name_length": 4}
{"curie": "MONDO:0021736", "names": ["Rectosigmoiditis", "rectosigmoiditis", "proctosigmoiditis", "Proctosigmoiditis", "Rectosigmoiditis, NOS", "Proctosigmoiditis, NOS", "Proctosigmoiditis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "proctosigmoiditis", "shortest_name_length": 16}
{"curie": "MONDO:0013255", "names": ["ARCS2", "arthrogryposis, renal dysfunction, and cholestasis 2", "ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2", "arthrogryposis, renal dysfunction, and cholestasis type 2", "VIPAS39 arthrogryposis-renal dysfunction-cholestasis syndrome", "arthrogryposis-renal dysfunction-cholestasis syndrome caused by mutation in VIPAS39"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis, renal dysfunction, and cholestasis 2", "shortest_name_length": 5}
{"curie": "UMLS:C5555950", "names": ["Broad Ligament Leiomyoma", "Broad ligament leiomyoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Broad ligament leiomyoma", "shortest_name_length": 24}
{"curie": "MONDO:0010353", "names": ["MRXSMP", "Martin Probst syndrome", "Martin-Probst syndrome", "MARTIN-PROBST SYNDROME", "martin-probst syndrome, X-linked recessive", "Martin-Probst deafness-mental retardation syndrome", "Martin-Probst Deafness-Mental Retardation Syndrome", "MARTIN-PROBST DEAFNESS-MENTAL RETARDATION SYNDROME", "X-linked deafness and intellectual disability syndrome", "Martin-Probst deafness-intellectual disability syndrome", "mental retardation, X-linked, syndromic, MARTIN-Probst type", "mental retardation, X-linked, syndromic, Martin-Probst type", "MENTAL RETARDATION, X-LINKED, SYNDROMIC, MARTIN-PROBST TYPE", "X-linked deafness-intellectual disability syndrome syndrome", "deafness-intellectual disability, Martin-Probst type syndrome", "deafness-intellectual disability syndrome, Martin-Probst type", "Deafness-intellectual disability syndrome, Martin-Probst type", "X-linked hearing loss-intellectual disability syndrome syndrome", "Deafness and intellectual disability Martin Probst type syndrome", "intellectual disability, X-linked, syndromic, Martin-Probst type", "intellectual disability, X-linked, syndromic, MARTIN-Probst type", "Hearing loss-intellectual disability syndrome, Martin-Probst type", "Deafness and intellectual disability Martin Probst type syndrome (disorder)", "Deafness and intellectual disability Martin Probst type syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness-intellectual disability, Martin-Probst type syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0020381", "names": ["patterned macular dystrophy", "macular dystrophy, patterned", "patterned dystrophy of retinal pigment epithelium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "patterned macular dystrophy", "shortest_name_length": 27}
{"curie": "MONDO:0030439", "names": ["SPGF57", "SPERMATOGENIC FAILURE 57", "spermatogenic failure 57"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 57", "shortest_name_length": 6}
{"curie": "UMLS:C0877690", "names": ["Renal graft loss"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal graft loss", "shortest_name_length": 16}
{"curie": "MONDO:0100175", "names": ["TTN myopathy", "TTN-related myopathy", "congenital myopathy related to TTN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "TTN-related myopathy", "shortest_name_length": 12}
{"curie": "UMLS:C4055178", "names": ["Cryoglobulinemic Glomerulonephritis Secondary to Systemic Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cryoglobulinemic Glomerulonephritis Secondary to Systemic Disease", "shortest_name_length": 65}
{"curie": "UMLS:C4521794", "names": ["Stage I Gastric (Stomach) Cancer", "Postneoadjuvant Therapy Stage I Gastric Cancer AJCC v8", "Postneoadjuvant Therapy Stage I Gastric Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postneoadjuvant Therapy Stage I Gastric Cancer AJCC v8", "shortest_name_length": 32}
{"curie": "UMLS:C5418782", "names": ["Recurrent Superficial Bladder Urothelial Carcinoma", "Recurrent Superficial Bladder Transitional Cell Carcinoma", "Recurrent Non-Muscle Invasive Bladder Urothelial Carcinoma", "Recurrent Non-Muscle Invasive Bladder Transitional Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Non-Muscle Invasive Bladder Urothelial Carcinoma", "shortest_name_length": 50}
{"curie": "UMLS:C1112349", "names": ["cord paralysis spinal", "spinal cord paralysis", "Spinal cord paralysis", "spinal cord; paralysis", "paralysis; spinal cord"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spinal cord paralysis", "shortest_name_length": 21}
{"curie": "DOID:14336", "names": ["estrogen excess", "excess estrogen", "Estrogen excess", "Estrogen Excess", "estrogen; excess", "Hyperestrogenism", "Oestrogen excess", "hyperestrogenism", "excess; estrogen", "Hyperoestrogenism", "estrogen; hypersecretion", "hypersecretion; estrogen", "Hyperestrogenism (disorder)", "hyperestrogenism (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "estrogen excess", "shortest_name_length": 15}
{"curie": "UMLS:C0863199", "names": ["Stage I Bladder Cancer without Cancer in situ", "Stage I Bladder Cancer without Carcinoma In Situ", "Carcinoma bladder stage I, without cancer in situ", "Bladder carcinoma stage I, without cancer in situ", "Stage I Bladder Carcinoma without Carcinoma in situ", "Stage I Bladder Cancer without Carcinoma In Situ AJCC v7", "Stage I Bladder Cancer without Carcinoma In Situ AJCC v6", "Carcinoma urinary bladder stage I, without cancer in situ", "Urinary bladder carcinoma stage I, without cancer in situ"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder carcinoma stage I, without cancer in situ", "shortest_name_length": 45}
{"curie": "MONDO:0043099", "names": ["Hordnes Engebretsen Knudtson syndrome", "acrobrachycephaly, ventriculomegaly, pulmonary stenosis, ectopic anus and mental retardation", "acrobrachycephaly, ventriculomegaly, pulmonary stenosis, ectopic anus and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hordnes Engebretsen Knudtson syndrome", "shortest_name_length": 37}
{"curie": "MONDO:0003729", "names": ["leukemia subleukemic", "Aleukemic Leukemia Cutis", "aleukemic leukemia cutis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aleukemic leukemia cutis", "shortest_name_length": 20}
{"curie": "UMLS:C0342496", "names": ["Micronodular Adrenal Disease", "Micronodular Adrenal Hyperplasia", "Micronodular adrenal hyperplasia", "Micronodular adrenal hyperplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Micronodular adrenal hyperplasia", "shortest_name_length": 28}
{"curie": "MONDO:0010123", "names": ["THUMB AGENESIS, SHORT STATURE, AND IMMUNODEFICIENCY", "Thumb Agenesis, Short Stature, And Immunodeficiency", "thumb agenesis, short stature, and immunodeficiency", "absent thumb-short stature-immunodeficiency syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "absent thumb-short stature-immunodeficiency syndrome", "shortest_name_length": 51}
{"curie": "UMLS:C4302554", "names": ["Reactive oxygen species 1 positive non-small cell lung cancer", "Reactive oxygen species 1 positive non-small cell lung cancer (disorder)", "Reactive oxygen species 1 positive non-small cell lung cancer (diagnosis)", "ROS1 positive NSCLC - reactive oxygen species 1 positive non-small cell lung cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reactive oxygen species 1 positive non-small cell lung cancer", "shortest_name_length": 61}
{"curie": "UMLS:C5191660", "names": ["MiNEN", "MINEN", "Mixed neuroendocrine-non neuroendocrine neoplasm", "Mixed Neuroendocrine Non-Neuroendocrine Neoplasm", "MiNEN - mixed neuroendocrine-non neuroendocrine neoplasm", "Mixed neuroendocrine-non neuroendocrine neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mixed neuroendocrine-non neuroendocrine neoplasm", "shortest_name_length": 5}
{"curie": "UMLS:C5447139", "names": ["Breast Angiolipoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Angiolipoma", "shortest_name_length": 18}
{"curie": "UMLS:C0278678", "names": ["metastatic kidney cancer", "kidney cancer, metastatic", "metastatic renal cell cancer", "Metastatic Renal Cell Cancer", "renal cell cancer, metastatic", "metastatic renal cell carcinoma", "renal cell carcinoma, metastatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Renal Cell Cancer", "shortest_name_length": 24}
{"curie": "UMLS:C1578691", "names": ["congenital myxedema", "Congenital myxedema", "congenital; myxedema", "myxedema; congenital", "Myxedema, Congenital", "Congenital myxoedema", "cretin; type myxedematous", "myxedematous; cretin (type)", "Myxedematous form of cretinism", "Myxoedematous form of cretinism", "Endemic cretinism, myxedematous type", "Endemic cretinism - myxedematous type", "Myxedematous form of endemic cretinism", "Endemic cretinism - myxoedematous type", "Myxoedematous form of endemic cretinism", "Myxedematous form of cretinism (disorder)", "congenital iodine-deficiency syndrome myxedematous type", "Congenital iodine-deficiency syndrome, myxedematous type", "Congenital iodine-deficiency syndrome, myxoedematous type", "Congenital iodine deficiency syndrome - myxedematous type", "deficiency; iodine, congenital syndrome, myxedematous type", "Congenital iodine deficiency syndrome - myxoedematous type", "iodine-deficiency; syndrome, congenital, myxedematous type", "syndrome; iodine-deficiency, congenital, myxedematous type", "Endemic congenital iodine deficiency syndrome of myxedematous type", "congenital iodine-deficiency syndrome myxedematous type (diagnosis)", "Endemic congenital iodine deficiency syndrome of myxoedematous type", "Endemic congenital iodine deficiency syndrome of myxedematous type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myxedema, Congenital", "shortest_name_length": 19}
{"curie": "MONDO:0008396", "names": ["Rutherfurd syndrome", "RUTHERFURD SYNDROME", "oculodental syndrome", "Oculodental syndrome", "Oculodental syndrome (disorder)", "Oculodental syndrome, Rutherfurd type", "oculodental syndrome, Rutherfurd type", "Gingival hypertrophy corneal dystrophy", "corneal dystrophy with gum hypertrophy", "Corneal dystrophy with gum hypertrophy", "gingival hypertrophy corneal dystrophy", "gingival hypertrophy-corneal dystrophy", "corneal dystrophy with gum Hypertrophy", "Gingival hypertrophy-corneal dystrophy", "CORNEAL DYSTROPHY WITH GUM HYPERTROPHY", "Oculodental syndrome Rutherfurd syndrome", "gingival Hypertrophy with corneal dystrophy", "GINGIVAL HYPERTROPHY WITH CORNEAL DYSTROPHY", "Gingival Hypertrophy With Corneal Dystrophy", "gingival hypertrophy-corneal dystrophy syndrome", "gingival fibromatosis-corneal dystrophy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculodental syndrome, Rutherfurd type", "shortest_name_length": 19}
{"curie": "MONDO:0004522", "names": ["Peritonitis", "peritonitis", "PERITONITIS", "Peritonitis NOS", "Peritonitis, NOS", "Peritonitis (disorder)", "Retractile mesenteritis", "Sclerosing Mesenteritis", "Sclerosing mesenteritis", "Lipomatous mesenteritis", "peritoneum inflammation", "sclerosing mesenteritis", "Unspecified peritonitis", "Peritoneal inflammation", "Retractile Mesenteritis", "peritonitis (diagnosis)", "retractile mesenteritis", "Mesenteric panniculitis", "Peritonitis, unspecified", "inflammation; peritoneum", "Mesenteritis, Retractile", "Mesenteritis, Sclerosing", "peritoneum; inflammation", "Mesenteric lipogranuloma", "IgG4-related mesenteritis", "Liposclerotic mesenteritis", "inflammation of peritoneum", "Other specified peritonitis", "acute generalized peritonitis", "primary bacterial peritonitis", "Inflammation of the peritoneum", "Peritonitis of unspecified cause", "Peritonitis of undetermined cause", "Isolated mesenteric lipodystrophy", "Sclerosing mesenteritis (disorder)", "Retractile mesenteritis (disorder)", "retractile mesenteritis (diagnosis)", "sclerosing mesenteritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peritonitis", "shortest_name_length": 11}
{"curie": "UMLS:C0280390", "names": ["Stage III Hypopharyngeal Epidermoid Carcinoma", "Stage III Epidermoid Carcinoma of Hypopharynx", "hypopharynx squamous cell carcinoma, stage III", "Stage III Hypopharyngeal Squamous Cell Carcinoma", "Stage III Squamous Cell Carcinoma of Hypopharynx", "Hypopharyngeal squamous cell carcinoma stage III", "Stage III Epidermoid Carcinoma of the Hypopharynx", "hypopharyngeal squamous cell carcinoma, stage III", "epidermoid carcinoma of the hypopharynx, stage III", "Stage III Hypopharyngeal Throat Squamous Cell Cancer", "Stage III Squamous Cell Carcinoma of the Hypopharynx", "Squamous cell carcinoma of the hypopharynx stage III", "stage III squamous cell carcinoma of the hypopharynx", "squamous cell carcinoma of the hypopharynx, stage III", "Stage III Hypopharyngeal Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypopharyngeal squamous cell carcinoma stage III", "shortest_name_length": 45}
{"curie": "UMLS:C3897230", "names": ["Untreated Gliomatosis Cerebri", "untreated childhood gliomatosis cerebri", "Untreated Childhood Gliomatosis Cerebri"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Untreated Childhood Gliomatosis Cerebri", "shortest_name_length": 29}
{"curie": "UMLS:C4683785", "names": ["RISS Stage III Plasma Cell Myeloma", "Revised International Staging System Stage IIII Plasma Cell Myeloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "RISS Stage III Plasma Cell Myeloma", "shortest_name_length": 34}
{"curie": "MONDO:0008419", "names": ["AIS", "IS1", "scoliosis, idiopathic 1", "adolescent isolated scoliosis", "ADOLESCENT ISOLATED SCOLIOSIS", "adolescent idiopathic scoliosis", "ADOLESCENT IDIOPATHIC SCOLIOSIS", "SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 1", "scoliosis, isolated, susceptibility to, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scoliosis, isolated, susceptibility to, 1", "shortest_name_length": 3}
{"curie": "UMLS:C5556869", "names": ["Major Salivary Gland Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Major Salivary Gland Squamous Cell Carcinoma", "shortest_name_length": 44}
{"curie": "UMLS:C0338339", "names": ["Recurrent Cerebral Astrocytoma", "recurrent childhood cerebral astrocytoma", "Recurrent Childhood Cerebral Astrocytoma", "recurrent pediatric cerebral astrocytoma", "pediatric cerebral astrocytoma, recurrent", "childhood cerebral astrocytoma, recurrent", "cerebral astrocytoma, childhood, recurrent", "cerebral astrocytoma, pediatric, recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Cerebral Astrocytoma", "shortest_name_length": 30}
{"curie": "UMLS:C0854769", "names": ["Recurrent Esophageal Squamous Cell Cancer", "Esophageal squamous cell carcinoma recurrent", "Recurrent Esophageal Squamous Cell Carcinoma", "Oesophageal squamous cell carcinoma recurrent", "Recurrent Squamous Cell Carcinoma of Esophagus", "Recurrent Squamous Cell Carcinoma of the Esophagus", "Esophageal squamous cell carcinoma site unspecified recurrent", "Oesophageal squamous cell carcinoma site unspecified recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal squamous cell carcinoma recurrent", "shortest_name_length": 41}
{"curie": "UMLS:C4528695", "names": ["stage IIIA Merkel cell carcinoma", "Pathologic Stage IIIA Merkel Cell Carcinoma AJCC v8", "pathologic stage IIIA Merkel cell carcinoma AJCC v8", "Pathologic Stage IIIA Neuroendocrine Carcinoma of the Skin AJCC v8", "pathologic stage IIIA neuroendocrine carcinoma of the skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IIIA Merkel Cell Carcinoma AJCC v8", "shortest_name_length": 32}
{"curie": "MONDO:0007435", "names": ["HRS", "NOD", "DRPLA", "Haw River Syndrome", "haw River syndrome", "Haw river syndrome", "HAW RIVER SYNDROME", "Haw River Syndromes", "River Syndromes, Haw", "Naito Oyanagi Disease", "Naito-Oyanagi Disease", "Naito Oyanagi disease", "Naito-Oyanagi disease", "NAITO-OYANAGI DISEASE", "Naito-Oyanagi Diseases", "Dentatorubropallidoluysian atrophy", "dentatorubral-pallidoluysian atrophy", "Dentatorubral-pallidoluysian atrophy", "Dentatorubral-Pallidoluysian Atrophy", "Dentatorubral pallidoluysian atrophy", "Dentatorubral Pallidoluysian Atrophy", "dentatorubral pallidoluysian atrophy", "DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY", "Atrophy, Dentatorubral-Pallidoluysian", "ataxia, chorea, seizures, and dementia", "Dentatorubral-Pallidoluysian Atrophies", "ATAXIA, CHOREA, SEIZURES, AND DEMENTIA", "Ataxia, Chorea, Seizures, And Dementia", "MYOCLONIC EPILEPSY WITH CHOREOATHETOSIS", "myoclonic epilepsy with choreoathetosis", "Atrophies, Dentatorubral-Pallidoluysian", "Dentatorubropallidoluysian degeneration", "Myoclonic epilepsy with choreoathetosis", "DRPLA - Dentatorubropallidoluysian atrophy", "Dentatorubral-pallidoluysian atrophy (DRPLA)", "dentatorubral-pallidoluysian atrophy (diagnosis)", "Dentatorubropallidoluysian degeneration (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dentatorubral-pallidoluysian atrophy", "shortest_name_length": 3}
{"curie": "MONDO:0019860", "names": ["thyroid hemiagenesis", "Thyroid hemiagenesis", "Congenital hemiagenesis of thyroid", "Congenital absence of half of thyroid", "Congenital absence of half of thyroid (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid hemiagenesis", "shortest_name_length": 20}
{"curie": "UMLS:C1883344", "names": ["Tissue Breakdown"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tissue Breakdown", "shortest_name_length": 16}
{"curie": "MONDO:0023011", "names": ["Wilson-Mikity", "Mikity-Wilson", "pulmonary dysmaturity", "Pulmonary dysmaturity", "Wilson-Mikity syndrome", "wilson-mikity syndrome", "wilson mikity syndrome", "dysmaturity; pulmonary", "pulmonary; dysmaturity", "Wilson Mikity syndrome", "Pulmonary dysmaturity syndrome", "syndrome; pulmonary dysmaturity", "Wilson-Mikity syndrome (disorder)", "Wilson-Mikity syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wilson-Mikity syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0002863", "names": ["mixed type rhabdomyosarcoma", "Mixed type rhabdomyosarcoma", "rhabdomyosarcoma; mixed type", "mixed; rhabdomyosarcoma (type)", "Mixed Alveolar Rhabdomyosarcoma", "mixed alveolar rhabdomyosarcoma", "mixed type alveolar rhabdomyosarcoma", "Mixed Type Alveolar Rhabdomyosarcoma", "mixed type rhabdomyosarcoma (diagnosis)", "Mixed type rhabdomyosarcoma (morphologic abnormality)", "malignant neoplasm myosarcoma rhabdomyosarcoma mixed type", "Rhabdomyosarcoma with Mixed Embryonal and Alveolar Features", "rhabdomyosarcoma with mixed embryonal and alveolar features", "Mixed embryonal rhabdomyosarcoma and alveolar rhabdomyosarcoma", "mixed embryonal rhabdomyosarcoma and alveolar rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rhabdomyosarcoma with mixed embryonal and alveolar features", "shortest_name_length": 27}
{"curie": "MONDO:0010489", "names": ["MRX101", "XLID101", "X-linked mental retardation 101", "mental retardation, X-linked 101", "MENTAL RETARDATION, X-LINKED 101", "intellectual disability, X-linked 101", "mental retardation, X-linked type 101", "intellectual disability, X-linked type 101", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 101", "non-syndromic X-linked intellectual disability 101", "MID2 non-syndromic X-linked intellectual disability", "intellectual developmental disorder, X-linked 101, X-linked recessive", "non-syndromic X-linked intellectual disability caused by mutation in MID2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 101", "shortest_name_length": 6}
{"curie": "UMLS:C4331345", "names": ["Stage IVB Unknown Primary Tumor (Except for EBV-Related and HPV-Related Tumors) and Metastatic Cervical Adenopathy AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Unknown Primary Tumor (Except for EBV-Related and HPV-Related Tumors) and Metastatic Cervical Adenopathy AJCC v8", "shortest_name_length": 122}
{"curie": "MONDO:0003053", "names": ["Choroid meningioma", "Choroid Plexus Meningioma", "choroid plexus meningioma", "Meningioma of Choroid Plexus", "meningioma of choroid plexus", "meningioma of the choroid plexus", "Meningioma of the Choroid Plexus", "meningioma of the Choroid Plexus", "choroid plexus meningioma (disease)", "meningioma (disease) of choroid plexus", "choroid meningioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choroid plexus meningioma", "shortest_name_length": 18}
{"curie": "MONDO:0017132", "names": ["hereditary ATTR amyloidosis", "familial TTR-related amyloidosis", "familial transthyretin-related amyloidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary ATTR amyloidosis", "shortest_name_length": 27}
{"curie": "UMLS:C1336194", "names": ["Stage IIB Retinoblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Retinoblastoma", "shortest_name_length": 24}
{"curie": "MONDO:0003718", "names": ["Precerebral artery occlusion", "precerebral artery occlusion", "occlusion precerebral artery", "occlusion; artery, precerebral", "artery; occlusion, precerebral", "artery; precerebral, occlusion", "Precerebral arterial occlusion", "Occlusion of precerebral artery", "Precerebral artery occlusion NOS", "Obstruction of precerebral artery", "Occlusion of precerebral artery, NOS", "Obstruction of precerebral artery, NOS", "precerebral artery occlusion (diagnosis)", "Precerebral arterial occlusion (disorder)", "Obstruction of precerebral artery (disorder)", "occlusion and stenosis of precerebral artery", "Occlusion and stenosis of precerebral arteries", "Occlusion and stenosis of precerebral artery NOS", "Occlusion and stenosis of unspecified precerebral artery", "occlusion and stenosis of precerebral artery (diagnosis)", "Occlusion and stenosis of multiple and bilateral precerebral arteries", "occlusion and stenosis of multiple and bilateral precerebral arteries"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "occlusion precerebral artery", "shortest_name_length": 28}
{"curie": "MONDO:0006109", "names": ["mixed Mesothelioma", "mixed mesothelioma", "Mixed Mesothelioma", "Biphasic mesothelioma", "Biphasic Mesothelioma", "biphasic mesothelioma", "biphasic; mesothelioma", "Mesothelioma, biphasic", "mesothelioma; biphasic", "Mesothelioma, biphasic, NOS", "Mesothelioma, biphasic type", "Malignant Mixed Mesothelioma", "malignant mixed mesothelioma", "Malignant Biphasic Mesothelioma", "malignant biphasic mesothelioma", "Malignant biphasic mesothelioma", "mesothelioma, biphasic, malignant", "Mesothelioma, biphasic, malignant", "Mesothelioma, biphasic type, malignant", "malignant biphasic mesothelioma, malignant", "Mesothelioma, biphasic, malignant (morphologic abnormality)", "mesothelioma, biphasic, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant biphasic mesothelioma", "shortest_name_length": 18}
{"curie": "MONDO:0015687", "names": ["CEL", "CELNOS", "eosinophilic leukemia", "Eosinophilic leukemia", "Eosinophilic Leukemia", "Chronic eosinophilic leukemia", "Chronic Eosinophilic Leukemia", "chronic eosinophilic leukemia", "chronic leukemia eosinophilic", "CEL/hypereosinophilic syndrome", "CEL/Hypereosinophilic syndrome", "Chronic eosinophilic leukaemia", "Chronic eosinophilic leukemia, NOS", "Chronic Eosinophilic Leukemia, NOS", "Chronic eosinophilic leukemia (disorder)", "chronic eosinophilic leukemia (diagnosis)", "Pdgfra-Associated Myeloproliferative Neoplasm", "Pdgfra-Associated Chronic Eosinophilic Leukemia", "Chronic Eosinophilic Leukemia, Not Otherwise Specified", "Chronic eosinophilic leukemia (morphologic abnormality)", "Chronic eosinophilic leukemia/hypereosinophilic syndrome", "chronic eosinophilic leukemia/hypereosinophilic syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic eosinophilic leukemia", "shortest_name_length": 3}
{"curie": "UMLS:C4527190", "names": ["Stage IV", "Stage IV Cutaneous (Skin) Melanoma", "Pathologic Stage IV Cutaneous Melanoma AJCC v8", "Pathologic Stage IV Melanoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IV Cutaneous Melanoma AJCC v8", "shortest_name_length": 8}
{"curie": "MONDO:0016057", "names": ["craniocele", "bifid cranium", "encephalocele", "cranium bifidum", "isolated encephalocele"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated encephalocele", "shortest_name_length": 10}
{"curie": "MONDO:0006405", "names": ["Salivary Gland Small Cell Carcinoma", "small cell salivary gland carcinoma", "salivary gland small cell carcinoma", "small cell carcinoma of salivary gland", "salivary gland neuroendocrine carcinoma", "neuroendocrine carcinoma of salivary gland", "saliva-secreting gland small cell carcinoma", "salivary gland anaplastic small cell carcinoma", "neuroendocrine carcinoma of the salivary gland", "small cell carcinoma of saliva-secreting gland", "anaplastic small cell carcinoma of salivary gland", "Salivary Gland Small Cell Neuroendocrine Carcinoma", "small cell carcinoma of salivary gland (diagnosis)", "anaplastic small cell carcinoma of the salivary gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "salivary gland small cell carcinoma", "shortest_name_length": 35}
{"curie": "MONDO:0003419", "names": ["Bartholin Gland Adenoma", "Bartholin gland adenoma", "Bartholin's gland adenoma", "Bartholin's Gland Adenoma", "major vestibular gland adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bartholin gland adenoma", "shortest_name_length": 23}
{"curie": "MONDO:0012448", "names": ["SPG33", "hereditary spastic paraplegia 33", "hereditary spastic paraplegia type 33", "ZFYVE27 hereditary spastic paraplegia", "autosomal dominant spastic paraplegia 33", "SPASTIC PARAPLEGIA 33, AUTOSOMAL DOMINANT", "Spastic Paraplegia 33, Autosomal Dominant", "spastic paraplegia 33, autosomal dominant", "hereditary spastic paraplegia caused by mutation in ZFYVE27"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 33", "shortest_name_length": 5}
{"curie": "UMLS:C1334440", "names": ["Lung Carcinoma Metastatic in the Bone", "Lung Carcinoma Metastatic to the Bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Carcinoma Metastatic in the Bone", "shortest_name_length": 37}
{"curie": "MONDO:0017809", "names": ["CLN12 disease", "parkinsonism due to ATP13A2 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parkinsonism due to ATP13A2 deficiency", "shortest_name_length": 13}
{"curie": "UMLS:C4281994", "names": ["Recurrent Lymphoplasmacytic Lymphoma", "Relapsed Lymphoplasmacytoid Lymphoma/Immunocytoma", "Recurrent Lymphoplasmacytoid Lymphoma/Immunocytoma", "Lymphoplasmacytoid lymphoma/immunocytoma recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoplasmacytoid lymphoma/immunocytoma recurrent", "shortest_name_length": 36}
{"curie": "MONDO:0010095", "names": ["Tapetoretinal Degeneration with Ataxia", "TAPETORETINAL DEGENERATION WITH ATAXIA", "tapetoretinal degeneration with ataxia", "ataxia-tapetoretinal degeneration syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ataxia-tapetoretinal degeneration syndrome", "shortest_name_length": 38}
{"curie": "MONDO:0020446", "names": ["coronary sinus stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coronary sinus stenosis", "shortest_name_length": 23}
{"curie": "UMLS:C3897759", "names": ["Recurrent Anaplastic Oligodendroglioma", "recurrent childhood anaplastic oligodendroglioma", "Recurrent Childhood Anaplastic Oligodendroglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Anaplastic Oligodendroglioma", "shortest_name_length": 38}
{"curie": "MONDO:0007126", "names": ["SPDA1", "BECHTEREW SYNDROME", "Bechterew syndrome", "ankylosing spondylitis 1", "MARIE-STRUMPELL SPONDYLITIS", "Marie-Strumpell spondylitis", "susceptibility to spondyloarthropathy 1", "spondyloarthropathy, susceptibility to, 1", "ANKYLOSING SPONDYLITIS, SUSCEPTIBILITY TO", "SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 1", "ankylosing spondylitis, susceptibility to", "HLA-B spondyloarthropathy, susceptibility to", "spondyloarthropathy, susceptibility to, type 1", "spondyloarthropathy, susceptibility to caused by mutation in HLA-B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloarthropathy, susceptibility to, 1", "shortest_name_length": 5}
{"curie": "UMLS:C0853936", "names": ["Complication of device removal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Complication of device removal", "shortest_name_length": 30}
{"curie": "MONDO:0009297", "names": ["GLYS", "GLYS1", "Glys1", "renal diabetes", "diabetes renal", "Renal diabetes", "renal; diabetes", "diabetes; renal", "Renal Glycosuria", "Renal Glucosuria", "GLYCOSURIA RENAL", "renal glucosuria", "Renal glycosuria", "RENAL GLYCOSURIA", "Renal glucosuria", "Glycosuria renal", "RENAL GLUCOSURIA", "renal glycosuria", "SGLT2 deficiency", "Glycosuria, Renal", "GLYCOSURIA, RENAL", "glycosuria, renal", "renal; glycosuria", "glycosuria; renal", "Renal glucosuria, NOS", "Renal glycosuria, NOS", "Familial renal glucosuria", "familial renal glucosuria", "Familial renal glycosuria", "Renal glycosuria (disorder)", "(Familial) renal glycosuria", "renal glycosuria (diagnosis)", "Familial renal glucosuria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial renal glucosuria", "shortest_name_length": 4}
{"curie": "MONDO:0004666", "names": ["Metagonimosis", "METAGONIMIASIS", "Metagonimiases", "Metagonimiasis", "metagonimiasis", "Metagonimus infestation", "Metagonimus; infestation", "infestation; Metagonimus", "metagonimiasis (diagnosis)", "Metagonimus yokogawai infection", "infections, Metagonimus yokogawai", "Infection by Metagonimus yokogawai", "infection by Metagonimus yokogawai", "Infection caused by Metagonimus yokogawai", "Infection caused by Metagonimus yokogawai (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metagonimiasis", "shortest_name_length": 13}
{"curie": "MONDO:0014918", "names": ["TROFAS", "THAUVIN-robinet-Faivre syndrome", "THAUVIN-ROBINET-FAIVRE SYNDROME", "Thauvin Robinet Faivre syndrome", "Thauvin-Robinet-Faivre syndrome", "Thauvin-robinet-Faivre syndrome", "Tall stature-intellectual disability-renal anomalies syndrome", "tall stature-intellectual disability-renal anomalies syndrome", "Tall stature, intellectual disability, renal anomalies syndrome", "Tall stature, intellectual disability, renal anomalies syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tall stature-intellectual disability-renal anomalies syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0013394", "names": ["HDBSCC", "porencephaly-microcephaly-bilateral congenital cataract syndrome", "HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION, AND CATARACTS", "hemorrhagic destruction of the brain, subependymal calcification, and cataracts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "porencephaly-microcephaly-bilateral congenital cataract syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0023619", "names": ["LMM", "SKLMM", "Lentigo maligna melanoma", "Lentigo Maligna Melanoma", "lentigo maligna melanoma", "Malignant Lentigo Melanoma", "malignant lentigo melanoma", "Hutchison melanotic freckle", "LMM - Lentigo maligna melanoma", "lentigo maligna melanoma of skin", "lentigo maligna malignant melanoma", "Lentigo maligna melanoma (disorder)", "melanoma, lentigo maligna malignant", "Melanoma in Hutchinson Melanotic Freckle", "lentigo maligna melanoma of skin (diagnosis)", "malignant melanoma, lentigo maligna malignant", "Lentigo maligna melanoma (morphologic abnormality)", "Malignant melanoma in Hutchinson melanotic freckle", "Malignant melanoma in Hutchinson's melanotic freckle"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lentigo maligna melanoma", "shortest_name_length": 3}
{"curie": "UMLS:C0854994", "names": ["Lung squamous cell carcinoma stage IV", "Metastatic Lung Squamous Cell Carcinoma", "Lung squamous cell carcinoma metastatic", "Squamous cell carcinoma of lung stage IV", "squamous cell carcinoma of lung with metastasis", "squamous cell carcinoma of lung with metastasis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung squamous cell carcinoma metastatic", "shortest_name_length": 37}
{"curie": "UMLS:C0677483", "names": ["carcinoma testes", "CARCINOMA TESTES", "Carcinoma testes", "carcinoma testis", "Carcinoma;testis", "carcinoma of testis", "testicular carcinoma", "TESTICULAR CARCINOMA", "carcinoma testicular", "carcinoma of the testis", "carcinoma of testis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carcinoma testes", "shortest_name_length": 16}
{"curie": "MONDO:0023048", "names": ["ectodermal dysplasia neurosensory deafness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia neurosensory deafness", "shortest_name_length": 42}
{"curie": "MONDO:0015243", "names": ["ABPA", "abpa", "Hinson-Pepys disease", "allergic aspergillosis", "Allergic aspergillosis", "pulmonary aspergillus disease", "allergic bronchopulmonary mycosis", "Bronchopulmonary aspergillosis allergic", "Bronchopulmonary Allergic Aspergilloses", "Bronchopulmonary Allergic Aspergillosis", "Allergic Bronchopulmonary Aspergillosis", "Allergic bronchopulmonary aspergillosis", "Allergic Bronchopulmonary Aspergilloses", "allergic bronchopulmonary aspergillosis", "Aspergilloses, Bronchopulmonary Allergic", "aspergillosis, allergic bronchopulmonary", "Bronchopulmonary Aspergillosis, Allergic", "Allergic Aspergilloses, Bronchopulmonary", "Aspergilloses, Allergic Bronchopulmonary", "Aspergillosis, Bronchopulmonary Allergic", "Aspergillosis, Allergic Bronchopulmonary", "Allergic Aspergillosis, Bronchopulmonary", "Bronchopulmonary Aspergilloses, Allergic", "ABPA - Allergic bronchopulmonary aspergillosis", "allergic bronchopulmonary aspergillosis (ABPA)", "allergic lung reaction to the fungus aspergillus", "allergic bronchopulmonary aspergillosis, familial", "ALLERGIC BRONCHOPULMONARY ASPERGILLOSIS, FAMILIAL", "Allergic bronchopulmonary aspergillosis (disorder)", "allergic bronchopulmonary aspergillosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "allergic bronchopulmonary aspergillosis", "shortest_name_length": 4}
{"curie": "MONDO:0017474", "names": ["Macrodactylia", "Macrodactyly of hand", "macrodactyly of hand", "Macrodactyly of hands", "Macrodactyly of finger", "Macrodactylia (fingers)", "macrodactylia of finger", "Macrodactyly of fingers", "macrodactyly of fingers", "Macrodactylia of fingers", "Macrodactyly of the hand", "macrodactyly of the hand", "Megalodactyly of the hand", "Megalodactylism of the hand", "megalodactylism of the hand", "Macrodactyly of hand (disorder)", "Macrodactylia of fingers (disorder)", "macrodactylia of finger (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macrodactyly of fingers", "shortest_name_length": 13}
{"curie": "MONDO:0016330", "names": ["acquired hypertrophic cardiomyopathy", "non-familial hypertrophic cardiomyopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-familial hypertrophic cardiomyopathy", "shortest_name_length": 36}
{"curie": "UMLS:C1334658", "names": ["Mediastinum", "Mediastinal Hodgkin Lymphoma", "Mediastinal Hodgkin's Disease", "Mediastinal Hodgkin's Lymphoma", "Hodgkin's Disease of Mediastinum", "Hodgkin's Lymphoma of Mediastinum", "Hodgkin's lymphoma of mediastinum", "Hodgkin's Disease of the Mediastinum", "Hodgkin's Lymphoma of the Mediastinum", "Primary Mediastinal Hodgkin's Lymphoma", "Hodgkin's lymphoma of mediastinum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's lymphoma of mediastinum", "shortest_name_length": 11}
{"curie": "MONDO:0000452", "names": ["PRMS", "progressive-relapsing MS", "Progressive-relapsing MS", "progressive relapsing multiple sclerosis", "multiple sclerosis progressive relapsing", "Progressive Relapsing Multiple Sclerosis", "Remittent-progressive multiple sclerosis", "Progressive relapsing multiple sclerosis", "Remittent Progressive Multiple Sclerosis", "Multiple Sclerosis, Progressive Relapsing", "Multiple Sclerosis, Remittent Progressive", "Progressive relapsing multiple sclerosis (disorder)", "Progressive relapsing multiple sclerosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive relapsing multiple sclerosis", "shortest_name_length": 4}
{"curie": "MONDO:0010723", "names": ["RP2", "Retinitis Pigmentosa 2", "RETINITIS PIGMENTOSA 2", "retinitis pigmentosa 2", "RP2 retinitis pigmentosa", "retinitis pigmentosa type 2", "RETINITIS PIGMENTOSA 2 (disorder)", "retinitis pigmentosa caused by mutation in RP2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 2", "shortest_name_length": 3}
{"curie": "MONDO:0006152", "names": ["pseudopolyposis; colon", "colon inflammatory polyp", "pseudopolyposis of colon", "Pseudopolyposis of colon", "Colon Inflammatory Polyp", "colonic inflammatory polyp", "Colonic Inflammatory Polyp", "Inflammatory Polyp of Colon", "inflammatory polyp of colon", "Inflammatory polyps of colon", "inflammatory polyps of colon", "Inflammatory Polyp of the Colon", "inflammatory polyp of the colon", "Inflammatory polyps of colon NOS", "Pseudopolyposis of colon (disorder)", "pseudopolyposis of colon (diagnosis)", "inflammatory polyps of colon (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colon inflammatory polyp", "shortest_name_length": 22}
{"curie": "MONDO:0021845", "names": ["Aloi Tomasini Isaia syndrome", "basal cell nevus anodontia abnormal bone mineralization", "Basal cell nevus, anodontia, abnormal bone mineralization", "basal cell nevus, anodontia, abnormal bone mineralization", "unilateral linear basal cell nevus associated with diffuse osteoma cutis, unilateral anodontia, and abnormal bone mineralization"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aloi Tomasini Isaia syndrome", "shortest_name_length": 28}
{"curie": "UMLS:C1142081", "names": ["CLL transformation", "Chronic lymphocytic leukemia transformation", "Chronic lymphocytic leukaemia transformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic lymphocytic leukemia transformation", "shortest_name_length": 18}
{"curie": "MONDO:0019210", "names": ["MCC", "mcc", "Merkle tumors", "Merkle Tumors", "Tumors, Merkle", "Apudoma of skin", "Cutaneous APUDoma", "merkel cell tumor", "Cutaneous Apudoma", "Merkel cell tumor", "Merkel Cell Tumor", "trabecular cancer", "cutaneous APUDoma", "cell merkel tumors", "Merkel Cell Cancer", "Tumor, Merkel Cell", "Merkel cell cancer", "Merkel cell tumour", "merkel cell tumour", "merkel cell cancer", "Cell Cancer, Merkel", "Cancer, Merkel Cell", "Merkel cell carcinoma", "Merkel Cell Carcinoma", "merkel cell carcinoma", "carcinoma, Merkel cell", "Carcinoma, Merkel Cell", "carcinoma cell merkels", "Merkel cell skin cancer", "carcinoma of Merkel cell", "trabecular skin carcinoma", "Trabecular Skin Carcinoma", "Merkel cell carcinoma NOS", "Apudoma of skin (disorder)", "Apudoma of skin (diagnosis)", "Neuroendocrine Skin Carcinoma", "neuroendocrine skin carcinoma", "carcinoma neuroendocrine skin", "cutaneous neuroendocrine tumor", "Merkel cell cancer of the skin", "adult neuroblastoma of the skin", "endocrine carcinoma of the skin", "trabecular carcinoma of the skin", "Anaplastic carcinoma of the skin", "Neuroendocrine Carcinoma of Skin", "Merkel cell carcinoma (disorder)", "Neuroendocrine tumor of the skin", "neuroendocrine carcinoma of skin", "Neuroendocrine tumour of the skin", "Trabecular cell carcinoma of skin", "Cutaneous neuroendocrine carcinoma", "cutaneous neuroendocrine carcinoma", "Cutaneous Neuroendocrine Carcinoma", "Neuroendocrine carcinoma of the skin", "Neuroendocrine Carcinoma of the Skin", "neuroendocrine carcinoma of the skin", "neuroendocrine tumor apudoma of skin", "primary small cell carcinoma of the skin", "Primary small cell carcinoma of the skin", "Primary cutaneous neuroendocrine carcinoma", "small cell neuroepithelial tumor of the skin", "Primary undifferentiated carcinoma of the skin", "Merkel cell carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous neuroendocrine carcinoma", "shortest_name_length": 3}
{"curie": "UMLS:C4288260", "names": ["STXBP2 Deficiency", "MUNC18-2 Deficiency", "MUNC18-2 Deficiency/STXBP2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "STXBP2 Deficiency", "shortest_name_length": 17}
{"curie": "MONDO:0001421", "names": ["Frontal Lobe Tumor", "frontal lobe tumor", "frontal lobe neoplasm", "Frontal Lobe Neoplasm", "Tumor of Frontal Lobe", "tumor of frontal lobe", "tumor of Frontal Lobe", "neoplasm of frontal lobe", "Neoplasm of Frontal Lobe", "Neoplasm of frontal lobe", "tumor of the frontal lobe", "Tumor of the Frontal Lobe", "Neoplasm of the Frontal Lobe", "neoplasm of the frontal lobe", "frontal lobe neoplasm (disease)", "neoplasm of frontal lobe of brain", "malignant neoplasm of frontal lobe", "Malignant neoplasm of frontal lobe", "Neoplasm of frontal lobe (disorder)", "malignant tumor of frontal lobe of brain", "malignant neoplasm of frontal lobe of brain", "Malignant neoplasm of frontal lobe (disorder)", "neoplasm of frontal lobe of brain (diagnosis)", "malignant neoplasm of frontal lobe of brain (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontal lobe neoplasm", "shortest_name_length": 18}
{"curie": "UMLS:C0863191", "names": ["stage IV stomach cancer", "Gastric carcinoma stage IV", "Stomach carcinoma stage IV NOS", "Gastric carcinoma stage IV NOS", "Stage IV Gastric Cancer AJCC v6", "Stomach Cancer Stage IV AJCC v6", "Stage IV Gastric (Stomach) Cancer", "Gastric Carcinoma Stage IV AJCC v6", "Stage IV Stomach Carcinoma AJCC v6", "Stage IV Gastric Carcinoma AJCC v6", "Stomach Carcinoma Stage IV AJCC v6", "Gastric Carcinoma, Stage IV AJCC v6", "Carcinoma of Stomach Stage IV AJCC v6", "Stage IV Carcinoma of Stomach AJCC v6", "Carcinoma of the Stomach Stage IV AJCC v6", "Stage IV Carcinoma of the Stomach AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric carcinoma stage IV", "shortest_name_length": 23}
{"curie": "UMLS:C0281464", "names": ["AIDS-related lymphoblastic lymphoma", "AIDS-Related Lymphoblastic Lymphoma", "AIDS Related Lymphoblastic lymphoma", "lymphoblastic lymphoma, AIDS-related", "AIDS Associated Lymphoblastic lymphoma", "AIDS-Associated Lymphoblastic lymphoma", "AIDS-associated lymphoblastic lymphoma", "AIDS-Related Precursor Lymphoblastic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Lymphoblastic Lymphoma", "shortest_name_length": 35}
{"curie": "UMLS:C4726548", "names": ["Refractory Head and Neck Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Head and Neck Carcinoma", "shortest_name_length": 34}
{"curie": "UMLS:C1520101", "names": ["Vulvar Tumor of Skin Appendage Origin", "Vulvar Neoplasm of Skin Appendage Origin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Neoplasm of Skin Appendage Origin", "shortest_name_length": 37}
{"curie": "UMLS:C4525119", "names": ["Stage II Colon Cancer", "Stage II Colon Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Colon Cancer AJCC v8", "shortest_name_length": 21}
{"curie": "MONDO:0100418", "names": ["AML, KIT exon 17 mutation", "AML, CD117 Exon 17 Mutation", "AML, c-KIT Exon 17 Mutation", "acute myeloid leukemia, KIT exon 17 mutation", "AML, KIT Proto-Oncogene Tyrosine Protein Kinase Gene Exon 17 Mutation", "AML, v-Kit Hardy-Zuckerman 4 Feline Sarcoma Viral Oncogene Homolog Gene Exon 17 Mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, KIT exon 17 mutation", "shortest_name_length": 25}
{"curie": "MONDO:0005112", "names": ["pleura mesothelioma", "Pleural mesothelioma", "pleural mesothelioma", "mesotheliomas pleural", "Mesothelioma of pleura", "PLEURAL MALIGNANT MESOTHELIOMA", "Malignant pleural mesothelioma", "Malignant Pleural Mesothelioma", "pleural malignant mesothelioma", "Pleural mesothelioma malignant", "Pleural Malignant Mesothelioma", "malignant pleural mesothelioma", "Pleural Mesothelioma, Malignant", "Malignant Pleural Mesotheliomas", "Mesothelioma, Malignant Pleural", "Malignant mesothelioma of pleura", "Pleural Mesotheliomas, Malignant", "Mesotheliomas, Malignant Pleural", "malignant mesothelioma of pleura", "Malignant Mesothelioma of Pleura", "malignant mesothelioma of the pleura", "Malignant Mesothelioma of the Pleura", "pleural diffuse malignant mesothelioma", "Pleural Diffuse Malignant Mesothelioma", "Malignant mesothelioma of pleura (disorder)", "malignant mesothelioma of pleura (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant pleural mesothelioma", "shortest_name_length": 19}
{"curie": "MONDO:0019026", "names": ["OPTB", "Severe osteopetrosis", "Malignant Osteopetrosis", "malignant osteopetrosis", "Osteopetrosis - precocious type", "Infantile malignant osteopetrosis", "Autosomal Recessive Osteopetrosis", "autosomal recessive osteopetrosis", "infantile malignant osteopetrosis", "osteopetrosis - autosomal recessive", "Autosomal recessive lethal osteopetrosis", "autosomal recessive osteopetrosis (disease)", "autosomal recessive malignant osteopetrosis", "Autosomal recessive malignant osteopetrosis", "osteopetrosis (disease), autosomal recessive", "Infantile malignant osteopetrosis (disorder)", "osteopetrosis - autosomal recessive (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive osteopetrosis", "shortest_name_length": 4}
{"curie": "MONDO:0100361", "names": ["lip herpes simplex type 1 infectious disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lip herpes simplex type 1 infectious disorder", "shortest_name_length": 45}
{"curie": "MONDO:0008308", "names": ["familial idiopathic priapism", "Familial idiopathic priapism", "PRIAPISM, FAMILIAL IDIOPATHIC", "priapism, familial idiopathic", "Priapism, familial idiopathic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "priapism, familial idiopathic", "shortest_name_length": 28}
{"curie": "MONDO:0020213", "names": ["stromal dystrophy", "corneal stromal dystrophy", "Corneal Stromal Dystrophy", "stromal corneal dystrophy", "Stromal corneal dystrophy", "Stromal Dystrophy, Corneal", "Dystrophy, Corneal Stromal", "Corneal Stromal Dystrophies", "Stromal Dystrophies, Corneal", "Stromal corneal dystrophy (disorder)", "stromal corneal dystrophy (diagnosis)", "stromal corneal dystrophy (physical finding)", "substantia propria of cornea corneal dystrophy (disease)", "corneal dystrophy (disease) of substantia propria of cornea"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stromal corneal dystrophy", "shortest_name_length": 17}
{"curie": "MONDO:0012847", "names": ["ARCI6", "autosomal recessive congenital ichthyosis 6", "ichthyosis, congenital, autosomal recessive 6", "ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6", "autosomal recessive congenital ichthyosis type 6", "ichthyosis, congenital, autosomal recessive type 6", "ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE, NIPAL4-RELATED", "ichthyosis, congenital, autosomal recessive, Nipal4-related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive congenital ichthyosis 6", "shortest_name_length": 5}
{"curie": "MONDO:0013184", "names": ["CTE", "IED", "DIAR5", "tufting enteropathy", "Tufting enteropathy", "congenital enteropathy", "EPCAM secretory diarrhea", "Congenital tufting enteropathy", "congenital tufting enteropathy", "Intestinal epithelial dysplasia", "intestinal epithelial dysplasia", "Enteropathy, Congenital Tufting", "ENTEROPATHY, CONGENITAL TUFTING", "enteropathy, congenital tufting", "INTESTINAL EPITHELIAL CELL DYSPLASIA", "Intestinal Epithelial Cell Dysplasia", "intestinal epithelial cell dysplasia", "Congenital epithelial dysplasia of intestine", "Non-syndromic congenital tufting enteropathy", "Diarrhea-5 with Congenital Tufting Enteropathy", "secretory diarrhea caused by mutation in EPCAM", "congenital diarrhea 5 with tufting enteropathy", "congenital diarrhoea 5 with tufting enteropathy", "DIARRHEA 5, WITH TUFTING ENTEROPATHY, CONGENITAL", "diarrhea 5, with tufting enteropathy, congenital", "Diarrhea 5, with Tufting Enteropathy, Congenital", "Diarrhea 5, With Tufting Enteropathy, Congenital", "Congenital epithelial dysplasia of intestine (disorder)", "congenital familial intractable diarrhea with enterocytes assembly abnormalities", "congenital familial intractable diarrhea with epithelial or epithelium abnormalities", "congenital familial intractable diarrhoea with epithelial or epithelium abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital diarrhea 5 with tufting enteropathy", "shortest_name_length": 3}
{"curie": "UMLS:C1332300", "names": ["Anosognostic Epilepsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anosognostic Epilepsy", "shortest_name_length": 21}
{"curie": "MONDO:0001112", "names": ["black death", "Black death", "BLACK DEATH", "black deaths", "black plague", "BUBONIC PLAGUE", "Bubonic Plague", "Bubonic plague", "bubonic plague", "bubonic; plague", "plague; bubonic", "PESTIS BUBONICA", "PLAGUE, BUBONIC", "PESTIS FULMINANS", "Bubonic plague (disorder)", "bubonic plague (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bubonic plague", "shortest_name_length": 11}
{"curie": "UMLS:C1257965", "names": ["Compensatory Hyperinsulinemia", "Hyperinsulinemia, Compensatory"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Compensatory Hyperinsulinemia", "shortest_name_length": 29}
{"curie": "MONDO:0008515", "names": ["Sd4", "SD4", "SDTY4", "syndactyly type 4", "Syndactyly type 4", "syndactyly, type 4", "syndactyly, type IV", "Syndactyly, Type IV", "SYNDACTYLY, TYPE IV", "Haas type syndactyly", "HAAS TYPE SYNDACTYLY", "Haas Type Syndactyly", "polysyndactyly type Haas", "POLYSYNDACTYLY, HAAS TYPE", "polysyndactyly, Haas type", "Polysyndactyly, Haas Type", "Polysyndactyly, Haas type", "Syndactyly type 4 (disorder)", "syndactyly type 4 (diagnosis)", "LMBR1 non-syndromic syndactyly", "non-syndromic syndactyly caused by mutation in LMBR1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndactyly type 4", "shortest_name_length": 3}
{"curie": "UMLS:C2111044", "names": ["Lacrimal Gland Follicular Lymphoma", "follicular lymphoma of lacrimal gland", "follicular lymphoma of lacrimal gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "follicular lymphoma of lacrimal gland", "shortest_name_length": 34}
{"curie": "UMLS:C5419207", "names": ["Unresectable Esophageal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Esophageal Squamous Cell Carcinoma", "shortest_name_length": 47}
{"curie": "OMIM:614490", "names": [], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"]}
{"curie": "MONDO:0005097", "names": ["LSCC", "LUSC", "epidermoid lung cancer", "lung cancer, epidermoid", "cancer cell lung squamous", "LUNG CANCER SQUAMOUS CELL", "lung cancer squamous cell", "squamous cell lung cancer", "squamous cell cancer lung", "Squamous Cell Lung Cancer", "Epidermoid carcinoma lung", "cancers cell lung squamous", "lung cancer, squamous cell", "cancer cells lung squamous", "cancer cell lungs squamous", "Squamous Cell Lung Carcinoma", "Lung Squamous Cell Carcinoma", "lung squamous cell carcinoma", "carcinoma cell lung squamous", "Epidermoid carcinoma of lung", "squamous cell lung carcinoma", "Squamous cell lung carcinoma", "squamous cell carcinoma lung", "carcinoma cell lungs squamous", "epidermoid cell lung carcinoma", "Epidermoid Cell Lung Carcinoma", "squamous cell carcinoma of lung", "Squamous Cell Carcinoma of Lung", "SQUAMOUS CELL CARCINOMA OF LUNG", "Squamous cell carcinoma of lung", "epidermoid cell carcinoma of lung", "Epidermoid Cell Carcinoma of Lung", "Squamous Cell Carcinoma of the Lung", "squamous cell carcinoma of the lung", "Epidermoid Cell Carcinoma of the Lung", "epidermoid cell carcinoma of the lung", "SCC - Squamous cell carcinoma of lung", "Epidermoid cell carcinoma of the lung", "non-oat cell lung cancer, squamous cell", "Squamous cell carcinoma of lung (disorder)", "squamous cell carcinoma of lung (diagnosis)", "Lung squamous cell carcinoma stage unspecified", "Squamous cell carcinoma of lung stage unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "squamous cell lung carcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0019418", "names": ["X-linked intellectual disability-epilepsy-progressive joint contractures-dysmorphism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability-epilepsy-progressive joint contractures-dysmorphism syndrome", "shortest_name_length": 93}
{"curie": "UMLS:C0581375", "names": ["TWO VESSEL DISEASE", "Two Vessel Coronary Disease", "Two coronary vessel disease", "Double coronary vessel disease", "2-vessel coronary artery stenosis", "Double vessel coronary artery disease", "Double coronary vessel disease (disorder)", "2-vessel coronary artery stenosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Double coronary vessel disease", "shortest_name_length": 18}
{"curie": "UMLS:C5238467", "names": ["Unresectable Midgut Neuroendocrine Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Midgut Neuroendocrine Tumor", "shortest_name_length": 40}
{"curie": "MONDO:0002289", "names": ["Iridopathy", "iris disease", "disease iris", "Iris Disease", "iris diseases", "Disease, Iris", "diseases iris", "Iris Diseases", "iris disorder", "Iris Disorder", "Iris disorder", "disorders iris", "Diseases, Iris", "disease of iris", "Disease of Iris", "Disorder of iris", "disorder of iris", "Iris disorder NOS", "Disorder of iris, NOS", "iris disease or disorder", "disease or disorder of iris", "Disorder of iris (disorder)", "disease (or disorder); iris"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "iris disorder", "shortest_name_length": 10}
{"curie": "UMLS:C0266998", "names": ["Oral soft tissue disease", "Oral soft tissue disorder", "disorder of oral soft tissue", "Disorder of oral soft tissues", "Oral soft tissue disorder NOS", "Disease of the oral soft tissues", "DISEASES OF THE ORAL SOFT TISSUES", "Disease of the oral soft tissues, NOS", "disorder of oral soft tissue (diagnosis)", "Disorder of oral soft tissues (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disorder of oral soft tissues", "shortest_name_length": 24}
{"curie": "UMLS:C0021376", "names": ["chronic inflammation", "inflammation chronic", "Chronic inflammation", "Chronic Inflammation", "Inflammation, chronic", "Chronic Inflammations", "CHRONIC INFLAMMATIONS", "chronic; inflammation", "inflammation; chronic", "Chronic inflammation, NOS", "Chronic inflammatory reaction", "Chronic inflammatory reaction, NOS", "Chronic inflammatory cell infiltration", "Inflammatory cell infiltration, chronic", "Chronic inflammatory cell infiltration, NOS", "Chronic inflammation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic inflammation", "shortest_name_length": 20}
{"curie": "UMLS:C4682808", "names": ["Stage IIIB Testicular Cancer", "Stage IIIB Testicular Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Testicular Cancer AJCC v8", "shortest_name_length": 28}
{"curie": "MONDO:0013533", "names": ["HL DEFICIENCY", "HL deficiency", "lipc deficiency", "LIPC DEFICIENCY", "HEPATIC LIPASE DEFICIENCY", "hepatic lipase deficiency", "Hepatic lipase deficiency", "hyperlipidemia due to HL deficiency", "Hyperlipidemia due to HL deficiency", "HEPATIC LIPASE DEFICIENCY (disorder)", "Hepatic lipase deficiency (disorder)", "hyperlipidemia due to HTGL deficiency", "Hyperlipidemia due to HTGL deficiency", "Hyperlipidemia due to hepatic lipase deficiency", "hyperlipidemia due to hepatic lipase deficiency", "hyperlipidemia due to hepatic triglyceride lipase deficiency", "Hyperlipidemia due to hepatic triglyceride lipase deficiency", "Hyperlipidaemia due to hepatic triglyceride lipase deficiency", "hyperlipidemia due to hepatic triacylglycerol lipase deficiency", "Hyperlipidemia due to hepatic triacylglycerol lipase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperlipidemia due to hepatic triglyceride lipase deficiency", "shortest_name_length": 13}
{"curie": "MONDO:0003073", "names": ["trilateral retinoblastoma", "Trilateral Retinoblastoma", "RETINOBLASTOMA, TRILATERAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trilateral retinoblastoma", "shortest_name_length": 25}
{"curie": "UMLS:C2747793", "names": ["Acute phosphate nephropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute phosphate nephropathy", "shortest_name_length": 27}
{"curie": "MONDO:0014074", "names": ["CMTDIF", "DI-CMTF", "Charcot-Marie-Tooth disease dominant intermediate F", "Charcot-Marie-Tooth disease, dominant intermediate F", "CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE F", "Charcot-Marie-Tooth disease dominant intermediate type F", "GNB4-related intermediate Charcot-Marie-Tooth neuropathy", "Charcot-Marie-Tooth disease, dominant Intermediate type F", "autosomal dominant intermediate Charcot-Marie-Tooth disease type F", "Charcot-Marie-Tooth disease autosomal dominant intermediate type F", "Autosomal dominant intermediate Charcot-Marie-Tooth disease type F", "Autosomal dominant intermediate Charcot-Marie-Tooth disease type F (disorder)", "Autosomal dominant intermediate Charcot-Marie-Tooth disease type F (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease dominant intermediate F", "shortest_name_length": 6}
{"curie": "UMLS:C5206464", "names": ["Metastatic Malignant Digestive System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Malignant Digestive System Neoplasm", "shortest_name_length": 46}
{"curie": "UMLS:C2987396", "names": ["Gastric Hepatoid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Hepatoid Adenocarcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0005843", "names": ["mediastinum tumor", "Mediastinal Tumor", "mediastinal tumor", "mediastinal cancer", "mediastinum tumors", "Mediastinal Cancer", "cancer mediastinal", "Mediastinum Cancer", "mediastinum cancer", "mediastinum tumours", "Mediastinal Cancers", "Mediastinum--Tumors", "Mediastinum Cancers", "Cancer, Mediastinum", "Cancer, Mediastinal", "Cancers, Mediastinum", "Tumor of Mediastinum", "tumor of mediastinum", "Cancers, Mediastinal", "Tumor of mediastinum", "Mediastinum Neoplasm", "Mediastinal Neoplasm", "Mediastinum neoplasm", "Mediastinal Neoplasms", "Neoplasm, Mediastinum", "tumour of mediastinum", "Neoplasm, Mediastinal", "Tumour of mediastinum", "Mediastinum Neoplasms", "cancer of mediastinum", "mediastinal neoplasms", "Cancer of Mediastinum", "Neoplasms, Mediastinal", "Neoplasms, Mediastinum", "neoplasm of mediastinum", "Neoplasm of Mediastinum", "Neoplasm of mediastinum", "Mediastinal neoplasm NOS", "Mediastinal Neoplasm NOS", "Tumor of the Mediastinum", "Cancer of the Mediastinum", "cancer of the mediastinum", "Malignant Mediastinal Tumor", "Neoplasm of the Mediastinum", "malignant mediastinal tumor", "Malignant mediastinal tumor", "Malignant mediastinal tumour", "Malignant mediastinal neoplasm", "malignant tumor of mediastinum", "Malignant tumor of mediastinum", "malignant mediastinum neoplasm", "malignant mediastinal neoplasm", "Malignant Mediastinal Neoplasm", "Malignant Tumor of Mediastinum", "Malignant tumour of mediastinum", "Mediastinal neoplasms malignant", "malignant neoplasm of mediastinum", "Malignant Neoplasm of Mediastinum", "Malignant neoplasm of mediastinum", "Neoplasm of mediastinum (disorder)", "Malignant Mediastinal Neoplasm NOS", "Malignant Tumor of the Mediastinum", "malignant tumor of the mediastinum", "Malignant mediastinal neoplasm NOS", "malignant mediastinal neoplasm NOS", "Malignant Neoplasm of the Mediastinum", "malignant neoplasm of the mediastinum", "Malignant neoplasm of mediastinum, NOS", "Malignant tumor of mediastinum (disorder)", "malignant neoplasm of mediastinum (diagnosis)", "Malignant neoplasm of mediastinum, part unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mediastinal cancer", "shortest_name_length": 17}
{"curie": "UMLS:C1333792", "names": ["Gastric Tubular Adenoma", "tubular adenoma of stomach", "Tubular Adenoma of Stomach", "Tubular Adenoma of the Stomach", "benign gastric tubular adenoma", "tubular adenoma of stomach (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tubular adenoma of stomach", "shortest_name_length": 23}
{"curie": "MONDO:0020544", "names": ["Streptococcal TSS", "streptococcal TSS", "Streptococcus toxic shock syndrome", "streptococcal toxic-shock syndrome", "Streptococcal toxic-shock syndrome", "Streptococcal toxic shock syndrome", "Toxic shock syndrome streptococcal", "streptococcal toxic shock syndrome", "Streptococcus caused toxic shock syndrome", "Streptococcal toxic shock syndrome (disorder)", "streptococcal toxic shock syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "streptococcal toxic-shock syndrome", "shortest_name_length": 17}
{"curie": "UMLS:C1335032", "names": ["Non-Neoplastic Pharyngeal Disease", "Non-Neoplastic Pharyngeal Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Pharyngeal Disorder", "shortest_name_length": 33}
{"curie": "UMLS:C0221725", "names": ["OBSTRUCTION BRONCHIAL", "bronchial obstruction", "Bronchial Obstruction", "Obstruction bronchial", "obstruction; bronchus", "Bronchial obstruction", "bronchus; obstruction", "BRONCHIAL OBSTRUCTION", "Obstruction of bronchus", "bronchial obstruction (diagnosis)", "Obstruction of bronchus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bronchial Obstruction", "shortest_name_length": 21}
{"curie": "MONDO:0009146", "names": ["Mikaelian syndrome", "ectodermal dysplasia and neurosensory deafness", "ECTODERMAL DYSPLASIA AND NEUROSENSORY DEAFNESS", "Ectodermal Dysplasia and Neurosensory Deafness", "congenital ectodermal dysplasia with hearing loss", "Congenital ectodermal dysplasia with hearing loss", "ectodermal dysplasia-sensorineural deafness syndrome", "ectodermal dysplasia-sensorineural hearing loss syndrome", "hidrotic ectodermal dysplasia, sensorineural hearing loss and contracture of the fifth fingers"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia-sensorineural deafness syndrome", "shortest_name_length": 18}
{"curie": "MONDO:0010654", "names": ["PRTS", "MRXS1", "Partington syndrome", "Partington-Mulley syndrome", "mental retardation, X-linked 36", "X-linked Russell-Silver syndrome", "intellectual disability, X-linked 36", "Partington syndrome, X-linked recessive", "mental retardation, X-linked, syndromic 1", "intellectual disability, X-linked, syndromic 1", "Partington X-linked mental retardation syndrome", "Partington X-linked intellectual disability syndrome", "X-linked intellectual disability-dystonia-dysarthria syndrome", "intellectual disability-dystonic movements-ataxia-seizures syndrome", "mental retardation, X-linked, with dystonic movements, ataxia, and seizures", "intellectual disability, X-linked, with dystonic movements, ataxia, and seizures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Partington syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0011414", "names": ["ASGD5", "anomaly peter", "Peter anomaly", "peters anomaly", "Peters anomaly", "Peters' anomaly", "Peter's anomaly", "peter's anomaly", "peters' anomaly", "anomaly; peter's", "anomalies peters", "Anomaly, Peters'", "Peters anomaly (disease)", "Peters congenital glaucoma", "Peters' anomaly (diagnosis)", "anterior segment dysgenesis 5", "ANTERIOR SEGMENT DYSGENESIS 5", "Irido-corneo-trabecular dysgenesis", "Irido-corneo-trabecular dysgenesis (disorder)", "anterior segment dysgenesis 5, multiple subtypes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peters anomaly", "shortest_name_length": 5}
{"curie": "MONDO:0056804", "names": ["peripheral nervous system benign neoplasm", "benign neoplasm of peripheral nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of peripheral nervous system", "shortest_name_length": 41}
{"curie": "MONDO:0011964", "names": ["CDG1J", "CDGIj", "CDG 1J", "CDG-Ij", "CDG Ij", "DPAGT1-CDG", "DPAGT1-CDG (CDG-Ij)", "CDG syndrome type Ij", "Congenital disorder of glycosylation 1j", "congenital disorder of glycosylation Ij", "DPAGT1-congenital disorder of glycosylation", "Congenital Disorder of Glycosylation Type Ij", "Congenital disorder of glycosylation type 1J", "Congenital disorder of glycosylation type Ij", "congenital disorder of glycosylation type Ij", "congenital disorder of glycosylation type 1j", "Congenital disorder of glycosylation type 1j", "Congenital Disorder of Glycosylation, Type IJ", "congenital disorder of glycosylation, type Ij", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij", "carbohydrate deficient glycoprotein syndrome type Ij", "Carbohydrate deficient glycoprotein syndrome type Ij", "Congenital disorder of glycosylation type 1j (disorder)", "Dolichyl-phosphate N-acetylgalactosamine phosphotransferase deficiency", "dolichyl-phosphate N-acetylgalactosamine phosphotransferase deficiency", "DPAGT1-CDG - dolichyl-phosphate n-acetylglucosamine phosphotransferase congenital disorder of glycosylation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DPAGT1-congenital disorder of glycosylation", "shortest_name_length": 5}
{"curie": "MONDO:0016345", "names": ["non-familial restrictive cardiomyopathy", "Non-familial restrictive cardiomyopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-familial restrictive cardiomyopathy", "shortest_name_length": 39}
{"curie": "MONDO:0002879", "names": ["uterine body mixed cancer", "malignant corpus uteri mixed tumor", "malignant uterine body mixed tumor", "Malignant Corpus Uteri Mixed Tumor", "Malignant Uterine Body Mixed Tumor", "malignant body of uterus mixed tumor", "Malignant Body of Uterus Mixed Tumor", "Malignant Uterine Corpus Mixed Tumor", "malignant uterine corpus mixed tumor", "malignant mixed tumor of Corpus Uteri", "malignant corpus uteri mixed neoplasm", "Malignant Uterine Body Mixed Neoplasm", "malignant uterine body mixed neoplasm", "Malignant Mixed Tumor of Corpus Uteri", "Malignant Mixed Tumor of Uterine Body", "malignant mixed tumor of uterine body", "malignant mixed tumor of corpus uteri", "Malignant Corpus Uteri Mixed Neoplasm", "malignant body of uterus mixed neoplasm", "malignant mixed tumor of uterine corpus", "Malignant Mixed Tumor of Body of Uterus", "malignant mixed tumor of body of uterus", "Malignant Body of Uterus Mixed Neoplasm", "Malignant Mixed Tumor of Uterine Corpus", "malignant mixed neoplasm of corpus uteri", "malignant mixed neoplasm of uterine body", "Malignant Mixed Neoplasm of Uterine Body", "Malignant Mixed Neoplasm of Corpus Uteri", "malignant mixed tumor of the corpus uteri", "Malignant Mixed Tumor of the Uterine Body", "Malignant Mixed Tumor of the Corpus Uteri", "malignant mixed tumor of the uterine body", "malignant mixed neoplasm of body of uterus", "malignant mixed neoplasm of uterine corpus", "Malignant Mixed Neoplasm of Uterine Corpus", "Malignant Mixed Neoplasm of Body of Uterus", "Malignant Mixed Tumor of the Uterine Corpus", "malignant mixed tumor of the uterine corpus", "Malignant Mixed Tumor of the Body of Uterus", "malignant mixed tumor of the body of uterus", "malignant mixed neoplasm of the uterine body", "Malignant Mixed Neoplasm of the Uterine Body", "malignant mixed neoplasm of the corpus uteri", "Malignant Mixed Neoplasm of the Corpus Uteri", "Malignant Mixed Neoplasm of the Body of Uterus", "Malignant Mixed Neoplasm of the Uterine Corpus", "malignant mixed neoplasm of the uterine corpus", "malignant mixed neoplasm of the body of uterus", "Malignant Uterine Corpus Mixed Epithelial and Mesenchymal Neoplasm", "malignant uterine corpus mixed epithelial and mesenchymal neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine body mixed cancer", "shortest_name_length": 25}
{"curie": "MONDO:0004147", "names": ["noninvasive thymoma", "non-invasive thymoma", "Noninvasive Malignant Thymoma", "Thymoma Malignant Noninvasive", "thymoma malignant noninvasive", "noninvasive malignant thymoma", "Thymoma malignant noninvasive", "Thymoma malignant Noninvasive", "malignant thymoma, noninvasive", "Malignant Thymoma, Noninvasive", "noninvasive thymoma and thymic carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "noninvasive malignant thymoma", "shortest_name_length": 19}
{"curie": "UMLS:C4528589", "names": ["Stage IIIA Breast Cancer", "Prognostic Stage IIIA Breast Cancer AJCC v8", "Prognostic Stage IIIA Breast Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prognostic Stage IIIA Breast Cancer AJCC v8", "shortest_name_length": 24}
{"curie": "MONDO:0017834", "names": ["HES-R", "secondary HES", "reactive hypereosinophilic syndrome", "secondary hypereosinophilic syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary hypereosinophilic syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0009231", "names": ["AMD2B", "DUPANS", "DU PAN SYNDROME", "Du Pan syndrome", "ACROMESOMELIC DYSPLASIA 2B", "acromesomelic dysplasia-2B", "acromesomelic dysplasia 2B", "Fibular aplasia and complex brachydactyly", "fibular hypoplasia and complex brachydactyly", "FIBULAR HYPOPLASIA AND COMPLEX BRACHYDACTYLY", "Fibular hypoplasia and complex brachydactyly", "Fibular aplasia-complex brachydactyly syndrome", "fibular aplasia-complex brachydactyly syndrome", "Aplasia of fibula co-occurrent with complex brachydactyly", "Aplasia of fibula co-occurrent with complex brachydactyly (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acromesomelic dysplasia 2B", "shortest_name_length": 5}
{"curie": "MONDO:0000633", "names": ["sense organ benign neoplasm", "sensory organ benign neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sensory organ benign neoplasm", "shortest_name_length": 27}
{"curie": "UMLS:C0796622", "names": ["Stage IIC Soft Tissue Sarcoma", "Stage IIC Sarcoma of Soft Tissue", "Stage IIC Sarcoma of the Soft Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIC Soft Tissue Sarcoma", "shortest_name_length": 29}
{"curie": "MONDO:0019882", "names": ["Trisomy 8qter", "trisomy 8qter", "distal trisomy 8q", "Distal trisomy 8q", "distal duplication 8q", "Distal duplication 8q", "distal trisomy type 8q", "Telomeric duplication 8q", "telomeric duplication 8q", "Distal trisomy 8q (disorder)", "Distal trisomy 8q (diagnosis)", "anomaly of chromosome 8 partial trisomy 8q distal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal trisomy 8q", "shortest_name_length": 13}
{"curie": "UMLS:C5236142", "names": ["Unresectable Malignant Peripheral Nerve Sheath Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Malignant Peripheral Nerve Sheath Tumor", "shortest_name_length": 52}
{"curie": "MONDO:0019761", "names": ["LTEC1", "LTEC I", "laryngotracheoesophageal cleft type 1", "laryngo-tracheo-esophageal cleft type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laryngotracheoesophageal cleft type 1", "shortest_name_length": 5}
{"curie": "UMLS:C4054324", "names": ["Obstructed Megaureter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Obstructed Megaureter", "shortest_name_length": 21}
{"curie": "MONDO:0007677", "names": ["glycinuria", "Glycinuria", "hyperglycinuria", "HYPERGLYCINURIA", "Hyperglycinuria", "Renal glycinuria", "Glycinuria (disorder)", "glycinuria (diagnosis)", "Iminoglycinuria type 2", "IMINOGLYCINURIA TYPE II", "Iminoglycinuria Type II", "Iminoglycinuria, type II", "hyperglycinuria (disease)", "High urine glycine levels", "HYPERGLYCINURIA (disorder)", "Glycinuria with or without Oxalate Urolithiasis", "glycinuria with or without oxalate urolithiasis", "GLYCINURIA WITH OR WITHOUT OXALATE UROLITHIASIS", "glycinuria with or without oxalate nephrolithiasis", "GLYCINURIA WITH OR WITHOUT OXALATE NEPHROLITHIASIS", "Glycinuria with or without Oxalate Nephrolithiasis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperglycinuria", "shortest_name_length": 10}
{"curie": "MONDO:0010640", "names": ["Loas", "LOAS", "LOAM", "Lhon, modifier of", "LHON, MODIFIER OF", "LEBER OPTIC ATROPHY, SUSCEPTIBILITY TO", "Leber optic atrophy, susceptibility to", "Leber hereditary optic neuropathy, modifier of", "LEBER HEREDITARY OPTIC NEUROPATHY, MODIFIER OF", "Leber hereditary optic neuropathy, modifier of, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leber optic atrophy, susceptibility to", "shortest_name_length": 4}
{"curie": "MONDO:0015099", "names": ["unilateral hemispheric polymicrogyria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "unilateral hemispheric polymicrogyria", "shortest_name_length": 37}
{"curie": "UMLS:C4329626", "names": ["Central Nervous System Anaplastic Large Cell Lymphoma, ALK-Positive", "Primary Central Nervous System Anaplastic Large Cell Lymphoma, ALK-Positive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Anaplastic Large Cell Lymphoma, ALK-Positive", "shortest_name_length": 67}
{"curie": "MONDO:0018002", "names": ["adult-onset CPEO with mitochondrial myopathy", "Adult-onset CPEO with mitochondrial myopathy", "adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy", "Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy", "Adult-onset CPEO (chronic progressive external ophthalmoplegia) with mitochondrial myopathy", "Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy", "shortest_name_length": 44}
{"curie": "MONDO:0016176", "names": ["axonal polyneuropathy associated with IgG/IgM/IgA monoclonal gammopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "axonal polyneuropathy associated with IgG/IgM/IgA monoclonal gammopathy", "shortest_name_length": 71}
{"curie": "MONDO:0001436", "names": ["hemosideroses", "Hemosideroses", "Hemosiderosis", "hemosiderosis", "HEMOSIDEROSIS", "Haemosiderosis", "HAEMOSIDEROSIS", "haemosiderosis", "Hemochromatosis", "hemochromatosis", "Hemosiderosis, NOS", "Haemosiderosis, NOS", "Hemosiderosis (disorder)", "hemosiderosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemosiderosis", "shortest_name_length": 13}
{"curie": "MONDO:0015028", "names": ["XXYY Syndrome", "syndrome xxyy", "Xxyy Syndrome", "XXYY syndrome", "xxyy syndrome", "Xxyy Syndromes", "Syndrome, Xxyy", "Syndromes, Xxyy", "48,XXYY Syndrome", "48,XXYY syndrome", "48, XXYY Syndrome", "48, XXYY syndrome", "XXYY syndrome (disorder)", "XXYY syndrome (diagnosis)", "48,XXYY Klinefelter syndrome", "48,XXYY variant of Klinefelter's syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "48,XXYY syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0011541", "names": ["CMD1J", "dilated cardiomyopathy 1J", "cardiomyopathy, dilated, 1J", "Cardiomyopathy, Dilated, 1J", "CARDIOMYOPATHY, DILATED, 1J", "dilated cardiomyopathy type 1J", "cardiomyopathy, dilated, type 1J", "EYA4 familial dilated cardiomyopathy", "neurosensory deafness with dilated cardiomyopathy", "sensorineural deafness with dilated cardiomyopathy", "neurosensory hearing loss with dilated cardiomyopathy", "sensorineural hearing loss with dilated cardiomyopathy", "familial dilated cardiomyopathy caused by mutation in EYA4", "autosomal dominant dilated cardiomyopathy with sensorineural hearing loss", "cardiomyopathy, dilated, with sensorineural hearing loss, autosomal dominant", "CARDIOMYOPATHY, DILATED, WITH SENSORINEURAL HEARING LOSS, AUTOSOMAL DOMINANT", "Cardiomyopathy, Dilated, with Sensorineural Hearing Loss, Autosomal Dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1J", "shortest_name_length": 5}
{"curie": "MONDO:0021948", "names": ["tuberculoderma", "Tuberculoderma", "skin tuberculose", "Skin Tuberculosis", "skin; tuberculous", "tuberculosis skin", "Skin Tuberculoses", "Skin tuberculosis", "skin tuberculosis", "Tuberculoses, Skin", "tuberculosis cutis", "tuberculosis; skin", "Tuberculosis, Skin", "Tuberculosis cutis", "Skin--Tuberculosis", "Tuberculosis, skin", "tuberculosis; cutis", "Tuberculosis of skin", "tuberculosis of skin", "Cutaneous Tuberculoses", "cutaneous tuberculosis", "Cutaneous tuberculosis", "Cutaneous Tuberculosis", "Tuberculosis, Cutaneous", "Tuberculoses, Cutaneous", "Tuberculosis of skin, NOS", "Tuberculosis of skin (disorder)", "cutaneous tuberculosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous tuberculosis", "shortest_name_length": 14}
{"curie": "UMLS:C0560258", "names": ["IgA Nephropathy, Liver Disease-associated", "IgA nephropathy associated with liver disease", "nephropathy IgA associated with liver disease", "IgA nephropathy associated with liver disease (diagnosis)", "Immunoglobulin A nephropathy associated with liver disease", "Immunoglobulin A nephropathy associated with liver disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IgA nephropathy associated with liver disease", "shortest_name_length": 41}
{"curie": "UMLS:C0184524", "names": ["Cerebral disorder", "Cerebral alteration", "Cerebral Alteration", "Cerebral disorder, NOS", "CEREBRAL ABNORMALITY NOS", "RNDx cerebral alteration", "Cerebral disease or syndrome", "Cerebral alteration (finding)", "Cerebral Diseases and Syndromes", "RNDx cerebral alteration (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebral alteration", "shortest_name_length": 17}
{"curie": "UMLS:C1541289", "names": ["Stage II Aggressive Non-Hodgkin Lymphoma", "Stage II Aggressive Adult Non-Hodgkin Lymphoma", "stage II aggressive adult non-Hodgkin lymphoma", "aggressive, stage II adult non-Hodgkin lymphoma", "Ann Arbor Stage II Aggressive Adult Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage II Aggressive Adult Non-Hodgkin Lymphoma", "shortest_name_length": 40}
{"curie": "MONDO:0005738", "names": ["HYDATIDOSIS", "hydatidosis", "Hydatidosis", "cyst hydatid", "hydatid cyst", "Echinococcus", "Hydatid cyst", "Echinococcosis", "echinococcosis", "ECHINOCOCCOSIS", "Echinococcoses", "HYDATID DISEASE", "Hydatid disease", "echinococciasis", "disease hydatid", "Disease;hydatid", "ECHINOCOCCIASIS", "Echinococciasis", "hydatid disease", "hydatid; disorder", "Echinococcosis NOS", "liver echinococcus", "echinococcal disease", "Echinococcus disease", "echinococcus disease", "hepatic echinococcosis", "echinococcus infection", "Echinococcus Infection", "Echinococcus Infections", "Echinococcosis of liver", "Infection, Echinococcus", "echinococcosis of liver", "pulmonary echinococcosis", "Echinococcosis (disorder)", "Echinococcosis, unspecified", "Tenia echinococcus infection", "Taenia echinococcus infection", "Echinococcus infectious disease", "Echinococcus disease or disorder", "echinococcus infection (diagnosis)", "echinococcosis, unspecified, of liver", "Echinococcus caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "echinococcosis", "shortest_name_length": 11}
{"curie": "UMLS:C0276688", "names": ["cryptococcal pneumonia", "Pneumonia cryptococcal", "Cryptococcal Pneumonia", "Cryptococcal pneumonitis", "PULMONARY CRYPTOCOCCOSIS", "Pulmonary cryptococcosis", "Pneumonitis cryptococcal", "PNEUMONIA FUNGAL CRYPTOCOCCAL", "cryptococcal pneumonia (diagnosis)", "Pulmonary cryptococcosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pulmonary cryptococcosis", "shortest_name_length": 22}
{"curie": "MONDO:0000663", "names": ["anosognosia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anosognosia", "shortest_name_length": 11}
{"curie": "UMLS:C4727713", "names": ["CIM", "Chemical Menopause", "Chemically-Induced Menopause", "Chemically Induced Menopause"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chemically-Induced Menopause", "shortest_name_length": 3}
{"curie": "UMLS:C1868905", "names": ["Intentional device misuse"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intentional device misuse", "shortest_name_length": 25}
{"curie": "MONDO:0002482", "names": ["Nipple Tumor", "nipple tumor", "tumor of Nipple", "Tumor of Nipple", "Nipple Neoplasm", "Nipple neoplasm", "nipple neoplasm", "tumor of nipple", "Neoplasm of Nipple", "neoplasm of nipple", "tumor of the nipple", "Tumor of the Nipple", "Neoplasm of the Nipple", "neoplasm of the nipple", "nipple benign neoplasm", "nipple neoplasm (disease)", "neoplasm of nipple (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nipple neoplasm", "shortest_name_length": 12}
{"curie": "MONDO:0005806", "names": ["hypopharynx cancer", "cancer hypopharynx", "Hypopharynx--Cancer", "hypopharyngeal cancer", "Hypopharyngeal Cancer", "Hypopharyngeal cancer", "cancer hypopharyngeal", "Cancer, Hypopharyngeal", "Hypopharyngeal Cancers", "hypural pharynx cancer", "Cancers, Hypopharyngeal", "Hypopharyngeal Neoplasms", "hypopharynx pharynx cancer", "pharynx cancer of hypopharynx", "malignant tumor of hypopharynx", "malignant Hypopharyngeal tumor", "Malignant tumor of hypopharynx", "Malignant Hypopharyngeal Tumor", "Malignant Tumor of Hypopharynx", "malignant hypopharyngeal tumor", "Malignant tumour of hypopharynx", "malignant tumour of hypopharynx", "Malignant neoplasm of hypopharynx", "Malignant Hypopharyngeal Neoplasm", "Malignant Neoplasm of Hypopharynx", "malignant hypopharyngeal neoplasm", "Malignant tumor of laryngopharynx", "malignant neoplasm of hypopharynx", "Malignant Tumor of the Hypopharynx", "Malignant tumour of laryngopharynx", "malignant tumor of the hypopharynx", "Malignant neoplasm of laryngopharynx", "Malignant neoplasm of hypopharynx NOS", "Malignant Neoplasm of the Hypopharynx", "malignant neoplasm of the hypopharynx", "Malignant neoplasm of hypopharynx, NOS", "Malignant tumor of hypopharynx (disorder)", "malignant neoplasm of hypopharynx (diagnosis)", "Malignant neoplasm of hypopharynx, unspecified", "Malignant tumor of posterior wall of hypopharynx", "malignant tumor of posterior wall of hypopharynx", "Malignant tumour of posterior wall of hypopharynx", "Malignant neoplasm of posterior hypopharyngeal wall", "Malignant neoplasm of posterior wall of hypopharynx", "malignant neoplasm of posterior wall of hypopharynx", "malignant neoplasm of posterior hypopharyngeal wall", "malignant hypopharyngeal neoplasm of posterior wall", "Malignant neoplasm of hypopharynx, unspecified site", "malignant neoplasm of other specified hypopharyngeal site", "malignant neoplasm of other specified sites of hypopharynx", "Malignant tumor of posterior wall of hypopharynx (disorder)", "malignant hypopharyngeal neoplasm of posterior wall (diagnosis)", "malignant neoplasm of ill-defined sites within the lip and oral cavity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypopharynx cancer", "shortest_name_length": 18}
{"curie": "UMLS:C3805040", "names": ["Phospholipidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Phospholipidosis", "shortest_name_length": 16}
{"curie": "MONDO:0024465", "names": ["SMDP2", "PULMONARY ALVEOLAR PROTEINOSIS, CONGENITAL, 2", "Pulmonary Alveolar Proteinosis, Congenital, 2", "pulmonary alveolar proteinosis, congenital, 2", "surfactant metabolism dysfunction, pulmonary, 2", "Surfactant Metabolism Dysfunction, Pulmonary, 2", "SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 2", "Interstitial lung disease due to SP-C deficiency", "SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 2 (disorder)", "INTERSTITIAL LUNG DISEASE DUE TO SURFACTANT PROTEIN C DEFICIENCY", "Interstitial Lung Disease Due To Surfactant Protein C Deficiency", "Interstitial lung disease due to surfactant protein C deficiency", "interstitial lung disease due to surfactant Protein C deficiency", "Interstitial lung disease due to SP-C (surfactant protein C) deficiency", "Interstitial lung disease due to surfactant protein C deficiency (disorder)", "Desquamative Interstitial Pneumonitis Due To Surfactant Protein C Deficiency", "desquamative interstitial pneumonitis due to surfactant Protein C deficiency", "DESQUAMATIVE INTERSTITIAL PNEUMONITIS DUE TO SURFACTANT PROTEIN C DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "surfactant metabolism dysfunction, pulmonary, 2", "shortest_name_length": 5}
{"curie": "MONDO:0002263", "names": ["GYN disorders", "Disease;genital;F", "Gynecologic Disease", "gynecologic diseases", "Gynecologic Diseases", "Gynecological disease", "GYNECOLOGIC DISORDERS", "gynecologic disorders", "disease gynecological", "gynecological disease", "Diseases, Gynecologic", "Gynaecological disease", "gynecological disorder", "Gynecological Disorder", "female genital disease", "Female Genital Disease", "diseases gynecological", "Genital Disease, Female", "diseases gynaecological", "Gynecological Disorders", "disease female genitals", "Genital disorder female", "Female Genital Diseases", "gynecological; disorder", "gynecological disorders", "disorders gynecological", "female genital diseases", "Female Genital Disorders", "female genital disorders", "Diseases, Female Genital", "Genital Diseases, Female", "disorders female genitals", "Gynecological disease, NOS", "Gynaecological disease, NOS", "female reproductive disease", "Genital disorder female NOS", "female genital tract disorder", "disorders female reproductive", "female reproductive disorders", "REPRODUCTIVE DISORDERS, FEMALE", "Disease of female genital organ", "Disorder of female genital tract", "disorder of female genital tract", "Disease of female genital system", "disease of female genital system", "genital organs; disorder, female", "Disorder of female genital system", "disorder of female genital system", "Diseases of female genital organs", "gynecologic disorders (diagnosis)", "Disorder of female genital organs", "female reproductive system disease", "Female Reproductive System Disease", "female reproductive system disorder", "Female Reproductive System Disorder", "Female reproductive system disorder", "DISEASES OF THE FEMALE GENITAL ORGANS", "disease of female reproductive system", "Disease of female genital organs, NOS", "Disorder of female genital organs, NOS", "disorder of female reproductive system", "Disorder of female reproductive system", "female genital tract disorder (diagnosis)", "Disorder of female genital tract (disorder)", "disease (or disorder); genital organ, female", "Disorder of female genital organs (disorder)", "Unspecified disorder of female genital organs", "female reproductive system disease or disorder", "Disorder of female reproductive system (disorder)", "disease or disorder of female reproductive system", "DISEASES OF THE FEMALE GENITAL ORGANS: GENERAL TERMS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "female reproductive system disorder", "shortest_name_length": 13}
{"curie": "UMLS:C1334975", "names": ["Non-Encapsulated Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Encapsulated Neoplasm", "shortest_name_length": 25}
{"curie": "UMLS:C2010353", "names": ["Gallbladder Large Cell NEC", "Gallbladder Large Cell Neuroendocrine Carcinoma", "large cell neuroendocrine carcinoma of gallbladder", "large cell neuroendocrine carcinoma of gallbladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "large cell neuroendocrine carcinoma of gallbladder", "shortest_name_length": 26}
{"curie": "MONDO:0001176", "names": ["Lens issue", "Lens disease", "Lens Disease", "lens disease", "Lens Diseases", "Lens disorder", "Lens Disorder", "Disease, Lens", "lens disorder", "Diseases, Lens", "Disorder of lens", "Disorders of lens", "Lens disorder NOS", "LENSE ABNORMALITIES", "DISORDERS OF THE LENS", "Disorder of lens, NOS", "Abnormality of the lens", "Abnormal lens morphology", "Disorder of lens (disorder)", "Disorders of lens (H25-H28)", "disorder of crystalline lens", "Unspecified disorder of lens", "Disorder of lens, unspecified", "lens of camera-type eye disease", "disease of lens of camera-type eye", "disorder of lens of camera-type eye", "disorder of crystalline lens (diagnosis)", "lens of camera-type eye disease or disorder", "disease or disorder of lens of camera-type eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lens disorder", "shortest_name_length": 10}
{"curie": "UMLS:C4049252", "names": ["Osteonecrosis of external auditory canal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Osteonecrosis of external auditory canal", "shortest_name_length": 40}
{"curie": "MONDO:0021838", "names": ["Al Gazali Khidr Prem Chandran syndrome", "Cherubism, optic atrophy and short stature", "cherubism, optic atrophy and short stature"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Al Gazali Khidr Prem Chandran syndrome", "shortest_name_length": 38}
{"curie": "UMLS:C5206438", "names": ["Stage IA2 Cervical Cancer FIGO 2018", "Stage IA2 Cervical Carcinoma FIGO 2018"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA2 Cervical Cancer FIGO 2018", "shortest_name_length": 35}
{"curie": "MONDO:0003957", "names": ["pineoblastoma", "Pineoblastoma", "adult pineoblastoma", "Adult Pineoblastoma", "pineoblastoma, adult", "pineoblastoma of adults"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult pineoblastoma", "shortest_name_length": 13}
{"curie": "UMLS:C3540839", "names": ["DWN", "Neonatal Drug Withdrawal", "Drug Withdrawal Syndrome in Newborn"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neonatal Drug Withdrawal", "shortest_name_length": 3}
{"curie": "MONDO:0014827", "names": ["SPG76", "hereditary spastic paraplegia 76", "hereditary spastic paraplegia type 76", "autosomal recessive spastic paraplegia 76", "spastic paraplegia 76, autosomal recessive", "SPASTIC PARAPLEGIA 76, AUTOSOMAL RECESSIVE", "Autosomal recessive spastic paraplegia type 76", "autosomal recessive spastic paraplegia type 76", "CAPN1 autosomal recessive complex spastic paraplegia", "Autosomal recessive spastic paraplegia type 76 (disorder)", "autosomal recessive complex spastic paraplegia caused by mutation in CAPN1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive spastic paraplegia type 76", "shortest_name_length": 5}
{"curie": "MONDO:0011113", "names": ["Cmt4c", "CMT4C", "CMT 4C", "Charcot Marie Tooth disease type 4C", "Charcot-Marie-Tooth disease type 4C", "Charcot-Marie-Tooth Disease Type 4C", "Charcot-Marie-Tooth disease, type 4C", "CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C", "Charcot-Marie-Tooth disease, Type 4C", "Charcot-Marie-Tooth neuropathy type 4C", "Charcot-Marie-Tooth neuropathy, type 4C", "Charcot-Marie-Tooth Neuropathy, Type 4c", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4C", "SH3TC2 Charcot-Marie-Tooth disease type 4", "Charcot-Marie-Tooth disease type 4C (disorder)", "Charcot-Marie-Tooth disease type 4C (diagnosis)", "Charcot-Marie-Tooth disease type 4 caused by mutation in SH3TC2", "autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4C", "Charcot-Marie-Tooth disease, demyelinating, autosomal recessive, type 4C", "CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, AUTOSOMAL RECESSIVE, TYPE 4C", "Charcot-Marie-Tooth Disease, Demyelinating, Autosomal Recessive, Type 4c"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 4C", "shortest_name_length": 5}
{"curie": "MONDO:0012870", "names": ["chromosome 2q31.2 deletion syndrome", "CHROMOSOME 2q31.2 DELETION SYNDROME", "Chromosome 2q31.2 Deletion Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 2q31.2 deletion syndrome", "shortest_name_length": 35}
{"curie": "UMLS:C1334773", "names": ["Minor Salivary Gland Mucoepidermoid Carcinoma", "Mucoepidermoid Carcinoma of Minor Salivary Gland", "Mucoepidermoid Carcinoma of the Minor Salivary Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Minor Salivary Gland Mucoepidermoid Carcinoma", "shortest_name_length": 45}
{"curie": "MONDO:0017351", "names": ["Lysine and hydroxylysine metabolism disorder", "lysine and hydroxylysine metabolism disorder", "Disorder of lysine and hydroxylysine metabolism", "disorder of lysine and hydroxylysine metabolism", "DISORDERS OF LYSINE AND HYDROXYLYSINE METABOLISM", "Disorders of lysine and hydroxylysine metabolism", "Disorder of lysine AND/OR hydroxylysine metabolism", "Disorder of lysine and hydroxylysine metabolism, NOS", "inborn disorder of lysine and hydroxylysine metabolism", "Disorder of lysine and hydroxylysine metabolism (disorder)", "Disorder of lysine AND/OR hydroxylysine metabolism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of lysine and hydroxylysine metabolism", "shortest_name_length": 44}
{"curie": "MONDO:0008660", "names": ["ADHR", "Autosomal dominant hypophosphatemia", "autosomal dominant hypophosphatemia", "Hypophosphatemia, Autosomal Dominant", "hypophosphatemia, autosomal dominant", "HYPOPHOSPHATEMIA, AUTOSOMAL DOMINANT", "Autosomal Dominant Hypophosphatemia Rickets", "Autosomal dominant hypophosphatemic rickets", "autosomal dominant hypophosphatemic rickets", "Autosomal Dominant Hypophosphatemic Rickets", "HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL DOMINANT", "hypophosphatemic rickets, autosomal dominant", "Hypophosphatemic Rickets, Autosomal Dominant", "Autosomal dominant hypophosphataemic rickets", "Autosomal Dominant Vitamin D-resistant Rickets", "Vitamin D-Resistant Rickets, Autosomal Dominant", "VITAMIN D-RESISTANT RICKETS, AUTOSOMAL DOMINANT", "vitamin D-resistant rickets, autosomal dominant", "Autosomal dominant hypophosphatemic rickets (disorder)", "autosomal dominant hereditary hypophosphatemic rickets", "hereditary hypophosphatemic rickets, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant hypophosphatemic rickets", "shortest_name_length": 4}
{"curie": "MONDO:0002171", "names": ["giant cell tumor", "Giant cell tumor", "cell giant tumor", "Giant Cell Tumor", "GIANT CELL TUMOR", "Tumor, Giant Cell", "Cell Tumor, Giant", "Giant cell tumour", "cells giant tumor", "Giant cell tumors", "giant cell tumour", "Giant Cell Tumors", "GIANT CELL TUMORS", "cell giant tumors", "giant cell tumors", "cells giants tumor", "Cell Tumors, Giant", "giant cell tumours", "Tumors, Giant Cell", "giant cell neoplasm", "Giant Cell Neoplasm", "GCT - Giant cell tumor", "Tumor, giant cell type", "Tumour, giant cell type", "GCT - Giant cell tumour", "tumor of the giant cell", "benign giant cell tumor", "Giant cell tumor (disorder)", "giant cell tumor (qualifier value)", "giant cell tumor (morphologic abnormality)", "Giant cell tumor (morphologic abnormality)", "giant cell tumors (morphologic abnormality)", "giant cell tumor NOS (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "giant cell tumor", "shortest_name_length": 16}
{"curie": "UMLS:C2938977", "names": ["Penile bruise", "Penile contusion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Penile contusion", "shortest_name_length": 13}
{"curie": "MONDO:0011882", "names": ["SFWHS", "skin fragility woolly hair syndrome", "SKIN FRAGILITY-WOOLLY HAIR SYNDROME", "Skin Fragility-Woolly Hair Syndrome", "skin fragility-woolly hair syndrome", "skin fragility-woolly hair-palmoplantar keratoderma syndrome", "skin fragility-woolly hair-palmoplantar hyperkeratosis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin fragility-woolly hair-palmoplantar keratoderma syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0033613", "names": ["CPSQ1", "NEDSWMA", "CPSQ1, FORMERLY", "cerebral palsy spastic quadriplegic", "Cerebral Palsy, Spastic Quadriplegic, 1", "cerebral palsy, spastic quadriplegic, 1", "cerebral palsy, spastic quadriplegic, type 1", "CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 1, FORMERLY", "neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities", "NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE SPASTICITY AND BRAIN WHITE MATTER ABNORMALITIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities", "shortest_name_length": 5}
{"curie": "EFO:1001516", "names": ["ovarian serous carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian serous carcinoma", "shortest_name_length": 24}
{"curie": "UMLS:C4745159", "names": ["Resectable Pancreatic Acinar Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Pancreatic Acinar Cell Carcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0007093", "names": ["AI4", "AIHHT", "DLX3 amelogenesis imperfecta", "amelogenesis imperfecta type 4", "amelogenesis imperfecta, type 4", "Amelogenesis Imperfecta, Type IV", "amelogenesis imperfecta, type IV", "AMELOGENESIS IMPERFECTA, TYPE IV", "amelogenesis imperfecta caused by mutation in DLX3", "hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism", "amelogenesis imperfecta hypomaturation-hypoplastic type with taurodontism", "Amelogenesis Imperfecta, Hypomaturation-Hypoplastic Type, with Taurodontism", "AMELOGENESIS IMPERFECTA, HYPOMATURATION-HYPOPLASTIC TYPE, WITH TAURODONTISM", "amelogenesis imperfecta, hypomaturation-hypoplastic type, with taurodontism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism", "shortest_name_length": 3}
{"curie": "MONDO:0008618", "names": ["Reinhardt-Pfeiffer syndrome", "Reinhardt Pfeiffer syndrome", "hypoplasia of ulna and fibula", "Hypoplasia of Ulna and Fibula", "ulna and fibula, hypoplasia OF", "Ulna And Fibula, Hypoplasia Of", "ULNA AND FIBULA, HYPOPLASIA OF", "REINHARDT-PFEIFFER MESOMELIC DYSPLASIA", "Reinhardt-Pfeiffer mesomelic dysplasia", "Reinhardt Pfeiffer mesomelic dysplasia", "Mesomelic dwarfism Reinhardt Pfeiffer type", "Mesomelic dwarfism Reinhardt-Pfeiffer type", "mesomelic dysplasia Reinhardt-Pfeiffer type", "Mesomelic dwarfism, Reinhardt-Pfeiffer type", "mesomelic dwarfism, Reinhardt-Pfeiffer type", "Reinhardt-Pfeiffer mesomelic skeletal dysplasia", "MESOMELIC DWARFISM OF HYPOPLASTIC ULNA AND FIBULA TYPE", "Mesomelic dwarfism of hypoplastic ulna and fibula type", "mesomelic dwarfism of hypoplastic ulna and fibula type", "Mesomelic dysplasia of hypoplastic ulna and fibula type", "Mesomelic dysplasia of hypoplastic ulna and fibula type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mesomelic dwarfism, Reinhardt-Pfeiffer type", "shortest_name_length": 27}
{"curie": "MONDO:0012754", "names": ["NNO3", "Nanophthalmos 3", "NANOPHTHALMIA 3", "nanophthalmos 3", "NANOPHTHALMOS 3", "Nanophthalmia 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nanophthalmos 3", "shortest_name_length": 4}
{"curie": "MONDO:0024288", "names": ["bilirubinemia", "Bilirubinemia", "BILIRUBINEMIA", "BILIRUBINAEMIA", "Bilirubinemias", "bilirubinaemia", "Bilirubinaemia", "hyperbilirubinemia", "Hyperbilirubinemia", "Bilirubinemia, NOS", "HYPERBILIRUBINEMIA", "hyperbilirubinaemia", "Hyperbilirubinemias", "Hyperbilirubinaemia", "HYPERBILIRUBINAEMIA", "hyperbilirubinemias", "Hyperbilirubinemia, NOS", "Hyperbilirubinemia (disorder)", "hyperbilirubinemia (diagnosis)", "Disorder characterized by elevated serum bilirubin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperbilirubinemia", "shortest_name_length": 13}
{"curie": "MONDO:0044037", "names": ["Livedo racemosa", "LIVEDO RACEMOSA", "livedo racemosa", "LIVEDO ANNULARIS", "Livedo reticularis", "LIVEDO RETICULARIS", "Livedo Reticularis", "livedo reticularis", "ASPHYXIA RETICULARIS", "asphyxia; reticularis", "reticularis; asphyxia", "Livedo reticularis, NOS", "Livedo reticularis (disorder)", "livedo reticularis (diagnosis)", "livedo reticularis (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "livedo reticularis", "shortest_name_length": 15}
{"curie": "MONDO:0019467", "names": ["BPDCN", "Blastic NK-cell lymphoma", "Blastic NK-Cell Lymphoma", "blastic NK-cell lymphoma", "Monomorphic NK-cell lymphoma", "Monomorphic NK-Cell Lymphoma", "monomorphic NK-cell lymphoma", "CD4+/CD56+ hematodermic neoplasm", "CD4+/CD56+ Hematodermic Neoplasm", "blastic plasmacytoid dendritic cell", "Blastic NK-cell lymphoma (diagnosis)", "Blastic Natural Killer Leukemia/Lymphoma", "blastic natural Killer leukemia/lymphoma", "Lymphoblastoid variant of NK-cell lymphoma", "lymphoblastoid variant of NK-cell lymphoma", "natural killer (NK) cell leukemia/lymphoma", "Agranular CD4+ Natural Killer Cell Leukemia", "agranular CD4+ natural Killer cell leukemia", "blastic plasmacytoid Dendritic cell neoplasm", "Blastic Plasmacytoid Dendritic Cell Neoplasm", "blastic plasmacytoid dendritic cell neoplasm", "Blastic plasmacytoid dendritic cell neoplasm", "agranular CD4+ CD56+ hematodermic neoplasm/tumor", "Agranular CD4+ CD56+ Hematodermic Neoplasm/Tumor", "early plasmacytoid Dendritic cell leukemia/lymphoma", "primary cutaneous CD4+/CD56+ hematolymphoid neoplasm", "Blastic plasmacytoid dendritic cell neoplasm (disorder)", "Blastic plasmacytoid dendritic cell neoplasm (diagnosis)", "Blastic plasmacytoid dendritic cell neoplasm (morphologic abnormality)", "neoplasm of hematopoietic cell type blastic plasmacytoid dendritic cell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CD4+/CD56+ hematodermic neoplasm", "shortest_name_length": 5}
{"curie": "UMLS:C0345918", "names": ["Ampullary carcinoma in situ", "Ampullary Carcinoma in Situ", "Stage 0 Ampullary Carcinoma", "Ampulla of Vater Cancer Stage 0", "Stage 0 Ampulla of Vater Cancer", "Stage 0 Ampulla of Vater Carcinoma", "ampulla of Vater carcinoma in situ", "Ampulla of Vater Carcinoma in situ", "carcinoma in situ of ampulla of Vater", "Carcinoma in situ of ampulla of Vater", "Stage 0 Ampulla of Vater Cancer AJCC v7", "Carcinoma in situ of ampulla of Vater (disorder)", "carcinoma in situ of ampulla of Vater (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carcinoma in situ of ampulla of Vater", "shortest_name_length": 27}
{"curie": "MONDO:0018276", "names": ["MDDG", "CMD due to dystroglycanopathy", "muscular dystrophy-dystroglycanopathy", "muscular dystrophy-dystroglycanopathy type B1", "congenital muscular dystrophy due to dystroglycanopathy", "Muscular dystrophy-dystroglycanopathy congenital with impaired intellectual development B1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy-dystroglycanopathy", "shortest_name_length": 4}
{"curie": "MONDO:0012038", "names": ["SSD", "Speech sound disorder", "speech-sound disorder", "Phonological Disorder", "SPEECH-SOUND DISORDER", "Speech Sound Disorder", "Disorder, Phonological", "Speech Sound Disorders", "Disorder, Speech Sound", "Phonological Disorders", "Disorders, Phonological", "Disorders, Speech Sound", "Speech-Sound Disorder, hereditary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "speech-sound disorder", "shortest_name_length": 3}
{"curie": "MONDO:0001609", "names": ["Schultz", "granulopenia", "Granulopenia", "AGRANULOCYTOSIS", "Agranulocytosis", "agranulocytoses", "Agranulocytoses", "Schultz disease", "agranulocytosis", "GRANULOCYTOPENIA", "granulocytopenia", "Granulocytopenia", "Granulocytopenias", "Granulocytopenic disorder", "Agranulocytosis (disorder)", "agranulocytosis (diagnosis)", "granulocytopenia (diagnosis)", "Granulocytopenic disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "agranulocytosis", "shortest_name_length": 7}
{"curie": "UMLS:C1333269", "names": ["Deletion of Chromosome 22 Associated Meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Deletion of Chromosome 22 Associated Meningioma", "shortest_name_length": 47}
{"curie": "UMLS:C1336716", "names": ["teratocarcinoma, testicular", "testis cancer, teratocarcinoma", "testicle cancer, teratocarcinoma", "testicular cancer, teratocarcinoma", "testicular embryonal carcinoma and teratoma", "testicular teratoma and embryonal carcinoma", "embryonal carcinoma and teratoma, testicular", "teratoma and embryonal carcinoma of the testis", "testis cancer, embryonal carcinoma and teratoma", "testis cancer, teratoma and embryonal carcinoma", "Mixed Embryonal Carcinoma and Teratoma of Testis", "Testicular Mixed Embryonal Carcinoma and Teratoma", "testicle cancer, teratoma and embryonal carcinoma", "testicular cancer, embryonal carcinoma and teratoma", "testicular cancer, teratoma and embryonal carcinoma", "Mixed Embryonal Carcinoma and Teratoma of the Testis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular Mixed Embryonal Carcinoma and Teratoma", "shortest_name_length": 27}
{"curie": "MONDO:0016424", "names": ["progressive neurosensory deafness-hypertrophic cardiomyopathy syndrome", "progressive sensorineural deafness-hypertrophic cardiomyopathy syndrome", "progressive neurosensory hearing loss-hypertrophic cardiomyopathy syndrome", "progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome", "shortest_name_length": 70}
{"curie": "MONDO:0006303", "names": ["Middle Ear Epidermoid Carcinoma", "middle Ear epidermoid carcinoma", "Epidermoid Carcinoma of Middle Ear", "Middle Ear Squamous Cell Carcinoma", "middle ear squamous cell carcinoma", "epidermoid carcinoma of middle Ear", "squamous cell carcinoma of middle ear", "Squamous Cell Carcinoma of Middle Ear", "squamous cell carcinoma of middle Ear", "epidermoid carcinoma of the middle Ear", "Epidermoid carcinoma of the middle ear", "epidermoid carcinoma of the middle ear", "Epidermoid Carcinoma of the Middle Ear", "Squamous Cell Carcinoma of the Middle Ear", "squamous cell carcinoma of the middle Ear", "squamous cell carcinoma of middle ear (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "middle ear squamous cell carcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C0020624", "names": ["light period", "scanty menses", "Scanty Menses", "Hypomenorrhea", "HYPOMENORRHEA", "Light periods", "periods light", "light periods", "hypomenorrhea", "Scanty period", "Scanty periods", "hypomenorrhoea", "Hypomenorrhoea", "HYPOMENORRHOEA", "scanty periods", "Hypomenorrhea NOS", "decrease menstruation", "MENSTRUATION DECREASE", "Light menstrual period", "Hypomenorrhea (finding)", "light menstrual periods", "Spotting only at periods", "hypomenorrhea (diagnosis)", "decreased or shortened menstrual flow", "less bleeding during menstrual period", "decreased bleeding during menstrual period", "less bleeding during menstrual period (symptom)", "less bleeding during menstrual period (hypomenorrhea)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypomenorrhea", "shortest_name_length": 12}
{"curie": "UMLS:C4525355", "names": ["IV", "Stage IV Intrahepatic Cholangiocarcinoma AJCC v8", "Stage IV Intrahepatic Bile Duct Cancer (Cholangiocarcinoma)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Intrahepatic Cholangiocarcinoma AJCC v8", "shortest_name_length": 2}
{"curie": "MONDO:0022603", "names": ["brachydactyly tibial hypoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly tibial hypoplasia", "shortest_name_length": 31}
{"curie": "UMLS:C4528576", "names": ["MPLC", "Multiple Primary Lung Cancers", "Malignant Neoplasm of Lung - Multiple Primary Sites"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Neoplasm of Lung - Multiple Primary Sites", "shortest_name_length": 4}
{"curie": "MONDO:0011131", "names": ["Todv syndrome", "TODV syndrome", "TODV SYNDROME", "Alves syndrome", "ALVES SYNDROME", "Alves-dos Santos-Castelo syndrome", "TRICHOOCULODERMOVERTEBRAL SYNDROME", "Trichooculodermovertebral syndrome", "Cote Adamopoulos Pantelakis syndrome", "tricho-oculo-dermo-vertebral syndrome", "ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA", "arthrogryposis and ectodermal dysplasia", "Arthrogryposis and ectodermal dysplasia", "ectodermal dysplasia - cataracts - kyphoscoliosis", "Arthrogryposis ectodermal dysplasia other anomalies", "ectodermal dysplasia-cataracts-kyphoscoliosis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tricho-oculo-dermo-vertebral syndrome", "shortest_name_length": 13}
{"curie": "UMLS:C4744862", "names": ["Metastatic Breast Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Breast Neuroendocrine Neoplasm", "shortest_name_length": 41}
{"curie": "UMLS:C1709049", "names": ["Mixed Epithelial and Mesenchymal Hair Follicle Tumor", "Mixed Epithelial and Mesenchymal Hair Follicle Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mixed Epithelial and Mesenchymal Hair Follicle Neoplasm", "shortest_name_length": 52}
{"curie": "UMLS:C1708785", "names": ["Lung Squamous Papilloma", "Lung Squamous Cell Papilloma", "Bronchial Squamous Cell Papilloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bronchial Squamous Cell Papilloma", "shortest_name_length": 23}
{"curie": "MONDO:0020388", "names": ["DORV with non-committed subpulmonary VSD", "double outlet right ventricle with non-committed subpulmonary ventricular septal defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "double outlet right ventricle with non-committed subpulmonary ventricular septal defect", "shortest_name_length": 40}
{"curie": "MONDO:0013810", "names": ["CDG2L", "CDGIIl", "CDG-IIL", "CDGIIdl", "CDG IIL", "CDG IIl", "COG6-CDG", "COG6-CGD", "COG6-CDG (CDG-IIL)", "CDG syndrome type IIL", "COG6-ongenital disorder of glycosylation", "COG6-congenital disorder of glycosylation", "Congenital disorder of glycosylation type 2l", "congenital disorder of glycosylation type 2l", "Congenital disorder of glycosylation type IIL", "congenital disorder of glycosylation type IIL", "congenital disorder of glycosylation type IIl", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl", "congenital disorder of glycosylation, type IIL", "Component of oligomeric golgi complex 6-congenital disorder of glycosylation", "Component of oligomeric golgi complex 6-congenital disorder of glycosylation (disorder)", "COG6-CGD - component of oligomeric golgi complex 6-congenital disorder of glycosylation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "COG6-ongenital disorder of glycosylation", "shortest_name_length": 5}
{"curie": "UMLS:C0238281", "names": ["Middle cerebral artery syndrome", "Middle Cerebral Artery Syndrome", "MIDDLE CEREBRAL ARTERY SYNDROME", "middle cerebral artery syndrome", "Middle cerebral artery syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Middle Cerebral Artery Syndrome", "shortest_name_length": 31}
{"curie": "UMLS:C0376323", "names": ["Edematous Ophthalmopathy", "Ophthalmopathy, Edematous", "Congestive Ophthalmopathy", "Edematous Ophthalmopathies", "Ophthalmopathy, Congestive", "Infiltrative Ophthalmopathy", "Congestive Ophthalmopathies", "Ophthalmopathy, Infiltrative", "Infiltrative Ophthalmopathies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congestive Ophthalmopathy", "shortest_name_length": 24}
{"curie": "UMLS:C0473120", "names": ["abdominal hematoma", "hematoma abdominal", "Abdominal hematoma", "abdominal haematoma", "Peritoneal hematoma", "abdominal hematomas", "Abdominal haematoma", "peritoneal hematoma", "Peritoneal haematoma", "Intra-abdominal hematoma", "Intra-abdominal haematoma", "Intra-abdominal hematoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intra-abdominal hematoma", "shortest_name_length": 18}
{"curie": "MONDO:0004058", "names": ["WDHA", "WDHH", "WDHA Syndrome", "WDHA syndrome", "wdha syndrome", "WDHA SYNDROME", "WDHA Syndromes", "Vipoma Syndrome", "Syndrome, Vipoma", "Pancreatic cholera", "pancreatic cholera", "Pancreatic Cholera", "PANCREATIC CHOLERA", "Cholera, Pancreatic", "Verner Morrison Syndrome", "Verner Morrison syndrome", "VERNER-MORRISON SYNDROME", "pancreatic WDHA syndrome", "Verner-Morrison syndrome", "werner morrison syndrome", "verner-morrison syndrome", "Pancreatic WDHA Syndrome", "Werner Morrison syndrome", "islet cell WDHA syndrome", "Verner-Morrison Syndrome", "Islet Cell WDHA Syndrome", "watery diarrhea syndrome", "Watery Diarrhea Syndrome", "verner morrison syndrome", "Syndrome, Verner-Morrison", "Pseudopancreatic cholera syndrome", "pancreatic cholera (WDHA syndrome)", "Verner-Morrison syndrome (disorder)", "watery diarrhea with hypokalemic alkalosis", "Watery Diarrhea with Hypokalemic Alkalosis", "Excessive vasoactive intestinal peptide secretion", "excessive vasoactive intestinal peptide secretion", "Verner-Morrison syndrome due to pancreatic neoplasm", "watery diarrhea, hypokalemia, and achlorhydria syndrome", "Watery Diarrhea, Hypokalemia, and Achlorhydria Syndrome", "Verner-Morrison syndrome due to pancreatic neoplasm (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic cholera", "shortest_name_length": 4}
{"curie": "MONDO:0024541", "names": ["THES1", "The syndrome", "diarrhea, syndromic", "trichohepatoenteric syndrome 1", "TRICHOHEPATOENTERIC SYNDROME 1", "TRICHOHEPATOENTERIC syndrome 1", "TTC37 tricho-hepato-enteric syndrome", "diarrhea, fatal infantile, with trichorrhexis nodosa", "tricho-hepato-enteric syndrome caused by mutation in TTC37"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichohepatoenteric syndrome 1", "shortest_name_length": 5}
{"curie": "UMLS:C0853694", "names": ["RhD HDN", "Rhesus Disease", "erythroblastosis; Rh", "rhesus; erythroblastosis", "Rhesus hemolytic disease of newborn", "Erythroblastosis Fetalis, Rh Disease", "RhD Hemolytic Disease of the Newborn", "Rhesus haemolytic disease of newborn", "Rhesus Hemolytic Disease of the Newborn", "Rhesus D Hemolytic Disease of the Newborn"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rhesus hemolytic disease of newborn", "shortest_name_length": 7}
{"curie": "MONDO:0003726", "names": ["breast apocrine adenosis", "Breast Apocrine Adenosis", "apocrine adenosis of breast", "Apocrine Adenosis of Breast", "Apocrine Adenosis of the Breast", "apocrine adenosis of the breast", "Apocrine Adenosis of the breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "apocrine adenosis of breast", "shortest_name_length": 24}
{"curie": "MONDO:0016919", "names": ["partial deletion of chromosome 21q", "partial monosomy of chromosome 21q", "partial monosomy of the long arm of chromosome 21", "partial deletion of the long arm of chromosome 21", "partial deletion of the long arm of chromosome type 21"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of the long arm of chromosome 21", "shortest_name_length": 34}
{"curie": "MONDO:0015713", "names": ["Idiopathic Central Precocious Puberty", "idiopathic central precocious puberty", "Idiopathic central precocious puberty", "Idiopathic central precocious puberty (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic central precocious puberty", "shortest_name_length": 37}
{"curie": "UMLS:C1333977", "names": ["Liver Cancer Secondary to Hepatitis B", "Hepatitis B Virus Related Hepatocellular Carcinoma", "Hepatitis B Virus-Related Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatitis B Virus-Related Hepatocellular Carcinoma", "shortest_name_length": 37}
{"curie": "UMLS:C5208245", "names": ["Immune-mediated thyroiditis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immune-mediated thyroiditis", "shortest_name_length": 27}
{"curie": "MONDO:0002142", "names": ["MFH", "UPS", "fibroxanthosarcoma", "Fibroxanthosarcoma", "Malignant Fibroxanthoma", "malignant fibroxanthoma", "Malignant fibroxanthoma", "Fibroxanthoma, malignant", "malignant fibrous cytoma", "Storiform-pleomorphic MFH", "Storiform-Pleomorphic MFH", "Fibrous histiocytoma malignant", "HISTIOCYTOMA MALIGNANT FIBROUS", "fibrous histiocytoma malignant", "Malignant fibrous histiocytoma", "malignant fibrous histiocytoma", "Malignant Fibrous Histiocytoma", "Fibrous Histiocytoma, Malignant", "fibrous histiocytoma, malignant", "Malignant Fibrous Histiocytomas", "Histiocytoma, Malignant Fibrous", "Fibrous histiocytomas malignant", "Fibrous histiocytoma, malignant", "histiocytoma, fibrous, malignant", "Histiocytoma, Fibrous, Malignant", "Fibrous Histiocytomas, Malignant", "Unclassified Pleomorphic Sarcoma", "unclassified pleomorphic sarcoma", "Malignant Fibrohistiocytic Tumor", "Histiocytomas, Malignant Fibrous", "Malignant Fibrohistiocytic Tumors", "malignant fibrohistiocytic tumors", "Fibrohistiocytic Tumor, Malignant", "Tumor, Malignant Fibrohistiocytic", "Fibrohistiocytic Tumors, Malignant", "Malignant fibrous histiocytoma NOS", "Tumors, Malignant Fibrohistiocytic", "adult malignant fibrous histiocytoma", "Undifferentiated Pleomorphic Sarcoma", "FIBROSARCOMA, PLEOMORPHIC, MALIGNANT", "Adult Malignant Fibrous Histiocytoma", "Undifferentiated pleomorphic sarcoma", "undifferentiated pleomorphic sarcoma", "malignant fibrous histiocytoma, adult", "adult unclassified pleomorphic sarcoma", "histiocytoma, malignant fibrous, adult", "Adult Unclassified Pleomorphic Sarcoma", "fibrous histiocytoma, malignant, adult", "Malignant fibrous histiocytoma (disorder)", "adult undifferentiated pleomorphic sarcoma", "Adult Undifferentiated Pleomorphic Sarcoma", "malignant fibrous histiocytoma (diagnosis)", "Storiform-Pleomorphic Fibrous Histiocytoma", "Storiform-pleomorphic fibrous histiocytoma", "fibroxanthosarcoma (morphologic abnormality)", "Undifferentiated high grade pleomorphic sarcoma", "Malignant fibrous histiocytoma stage unspecified", "Undifferentiated Pleomorphic Soft Tissue Sarcoma", "undifferentiated pleomorphic soft tissue sarcoma", "Unclassified Pleomorphic sarcoma (formerly \"MFH\")", "Unclassified Pleomorphic Sarcoma (Formerly \"MFH\")", "Storiform-Pleomorphic Malignant Fibrous Histiocytoma", "Storiform-pleomorphic malignant fibrous histiocytoma", "Malignant Fibrous Histiocytoma of Soft Tissue and Bone", "malignant fibrous histiocytoma of soft tissue and bone", "Fibrous histiocytoma, malignant (morphologic abnormality)", "fibrous histiocytoma, malignant (morphologic abnormality)", "Malignant Fibrous Histiocytoma of the Soft Tissue and Bone", "malignant fibrous histiocytoma of the soft tissue and bone", "Unclassified Pleomorphic Sarcoma (Formerly \"Malignant Fibrous Histiocytoma\")", "Unclassified Pleomorphic sarcoma (formerly \"malignant fibrous histiocytoma\")", "undifferentiated pleomorphic sarcoma/malignant fibrous histiocytoma/high-grade spindle cell sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "undifferentiated pleomorphic sarcoma", "shortest_name_length": 3}
{"curie": "UMLS:C0855195", "names": ["Stage II Testicular Embryonal Carcinoma", "Testicular embryonal carcinoma stage II", "Stage II Testicular Embryonal Carcinoma AJCC v6", "Stage II Testicular Embryonal Carcinoma AJCC v7", "Stage II Testicular Embryonal Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular embryonal carcinoma stage II", "shortest_name_length": 39}
{"curie": "UMLS:C1709657", "names": ["Primary Cutaneous Diffuse Large B-Cell Lymphoma, Other"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Cutaneous Diffuse Large B-Cell Lymphoma, Other", "shortest_name_length": 54}
{"curie": "MONDO:0044640", "names": ["CMT2T", "AR-CMT2T", "Charcot-Marie-Tooth disease type 2T", "autosomal recessive axonal Charcot-Marie-Tooth disease type 2T"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 2T", "shortest_name_length": 5}
{"curie": "MONDO:0020120", "names": ["Rhabdomyopathy", "Skeletal myopathy", "skeletal muscle disorder", "Disease of skeletal muscle", "Disorder of skeletal muscle", "skeletal muscle tissue disease", "disease of skeletal muscle tissue", "disorder of skeletal muscle tissue", "Disorder of skeletal muscle (disorder)", "skeletal muscle tissue disease or disorder", "disease or disorder of skeletal muscle tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skeletal muscle disorder", "shortest_name_length": 14}
{"curie": "MONDO:0016103", "names": ["HyperCKmia", "hyperCKmia", "elevated serum CPK", "isolated hyperCKemia", "Isolated HyperCKemia", "idiopathic hyperCKemia", "isolated asymptomatic hyperCKemia", "idiopathic asymptomatic hyperCKemia", "isolated elevated serum creatine phosphokinase levels", "isolated asymptomatic elevation of creatine phosphokinase"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated asymptomatic elevation of creatine phosphokinase", "shortest_name_length": 10}
{"curie": "MONDO:0045060", "names": ["cribriform DCIS of breast", "Cribriform DCIS of Breast", "cribriform DCIS of the breast", "Cribriform DCIS of the Breast", "DCIS of breast with cribriform pattern", "DCIS of Breast with Cribriform Pattern", "cribriform ductal breast carcinoma in situ", "DCIS of the breast with cribriform pattern", "Cribriform Ductal Breast Carcinoma in situ", "DCIS of the Breast with Cribriform Pattern", "Intraductal Cribriform Breast Adenocarcinoma", "Breast Intraductal Cribriform Adenocarcinoma", "intraductal cribriform breast adenocarcinoma", "cribriform ductal carcinoma in situ of breast", "Cribriform Ductal Carcinoma in situ of Breast", "non-invasive cribriform ductal breast carcinoma", "Non-Invasive Cribriform Ductal Breast Carcinoma", "Breast Ductal Carcinoma In Situ, Cribriform Type", "cribriform ductal carcinoma in situ of the breast", "Cribriform Ductal Carcinoma in situ of the Breast", "Breast Ductal Carcinoma In Situ, Cribriform Pattern", "non-infiltrating cribriform ductal breast carcinoma", "Non-Infiltrating Cribriform Ductal Breast Carcinoma", "Breast Ductal Carcinoma In Situ with Cribriform Pattern", "Ductal Carcinoma in situ of Breast with Cribriform Pattern", "ductal carcinoma in situ of breast with cribriform pattern", "Ductal Carcinoma in situ of the Breast with Cribriform Pattern", "ductal carcinoma in situ of the breast with cribriform pattern"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intraductal cribriform breast adenocarcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0010887", "names": ["hairy throat", "Hairy throat", "hairy throat syndrome", "Hairy throat syndrome", "Tsukahara Kajii syndrome", "Tsukahara-Kajii syndrome", "anterior cervical hypertrichosis", "Anterior cervical hypertrichosis", "Hypertrichosis, anterior cervical", "hypertrichosis, anterior cervical", "HYPERTRICHOSIS, ANTERIOR CERVICAL", "Congenital cervical hypertrichosis", "isolated anterior cervical hypertrichosis", "Isolated anterior cervical hypertrichosis", "Hypertrichosis, congenital anterior cervical", "Isolated anterior cervical hypertrichosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated anterior cervical hypertrichosis", "shortest_name_length": 12}
{"curie": "UMLS:C0854750", "names": ["recurrent colorectal cancer", "Colorectal cancer recurrent", "Recurrent Colorectal Cancer", "colorectal cancer recurrent", "Colorectal Cancer, Recurrent", "Colorectal Carcinoma Recurrent", "Recurrent Colorectal Carcinoma", "Recurrent Colorectal (Colon or Rectal) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal cancer recurrent", "shortest_name_length": 27}
{"curie": "MONDO:0013069", "names": ["OPA7", "optic atrophy 7", "Optic Atrophy 7", "autosomal recessive optic atrophy, OPA7 type", "optic atrophy 7 with or without auditory neuropathy", "OPTIC ATROPHY 7 WITH OR WITHOUT AUDITORY NEUROPATHY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive optic atrophy, OPA7 type", "shortest_name_length": 4}
{"curie": "UMLS:C4054278", "names": ["P3 Hydronephrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "P3 Hydronephrosis", "shortest_name_length": 17}
{"curie": "MONDO:0001794", "names": ["CRABS", "Crabs", "crabs", "pubic lice", "Pubic lice", "Pubic Lice", "Phthiriasis", "Pubic louse", "phthiriasis", "Phthiriosis", "pubic louse", "Phthirus pubis", "phthirus pubis", "Pediculus pubis", "PUBIC HAIR LICE", "lice; pubic lice", "crab infestation", "pediculosis pubis", "Pediculosis pubis", "PEDICULOSIS PUBIS", "phthiriasis pubis", "Phthiriasis pubis", "Crabs infestation", "Pubis pediculosis", "PHTHIRIASIS PUBIS", "Pediculosis Pubis", "Crabs - pubic lice", "infestation; Phthirus", "PEDICULOSIS, INGUINAL", "crab lice infestation", "Phthirus; infestation", "pubic lice infestation", "pubic lice; infestation", "Pthirus pubis infection", "Pubic louse infestation", "Infestation by Phthirus", "infestation; pubic lice", "Infestation by crab lice", "infections, Pthirus pubis", "Pthirus pubis infestation", "Infestation by crab-louse", "Phthirus pubis; pediculosis", "Infestation (by);lice;pubic", "pediculosis; Phthirus pubis", "Phthirus pubis - pubic lice", "Pediculus pubis - pubic lice", "Infestation by Phthirus, NOS", "Phthirus pubis [pubic louse]", "infestation by Phthirus pubis", "pubic lice (physical finding)", "pediculosis pubis (diagnosis)", "Infestation by Phthirus pubis", "Infestation caused by Phthirus", "Infestation caused by crab lice", "Infestation caused by Phthirus pubis", "Infestation caused by Phthirus (disorder)", "Phthirus/pediculus pubis - pubic lice - crabs", "Infestation caused by Phthirus pubis (disorder)", "Phthirus/pediculus pubis - pubic lice - crabs (& infestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pthirus pubis infestation", "shortest_name_length": 5}
{"curie": "MONDO:0030990", "names": ["KTZSL", "Kohlschutter-Tonz syndrome-like", "KOHLSCHUTTER-TONZ SYNDROME-LIKE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kohlschutter-Tonz syndrome-like", "shortest_name_length": 5}
{"curie": "UMLS:C5420758", "names": ["Conjunctival Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conjunctival Carcinoma", "shortest_name_length": 22}
{"curie": "MONDO:0008243", "names": ["Pick disease", "PICK DISEASE", "pick disease", "Pick Disease", "picks disease", "Picks Disease", "Disease, Pick", "disease picks", "syndrome; Pick", "Pick's disease", "pick's disease", "pick s disease", "Pick's Disease", "Disease, Pick's", "brain; disease, Pick", "Lobar Atrophy (Brain)", "Pick Disease Of Brain", "PICK DISEASE OF BRAIN", "PICK disease of brain", "lobar atrophy of brain", "Lobar cerebral atrophy", "Lobar Atrophy Of Brain", "LOBAR ATROPHY OF BRAIN", "Picks Disease of Brain", "Atrophy, Lobar (Brain)", "Lobar Atrophies (Brain)", "frontotemporal dementia", "dementia frontotemporal", "Atrophies, Lobar (Brain)", "Pick Disease of the Brain", "Pick; disease or syndrome", "Pick disease of the brain", "Pick's disease (diagnosis)", "lobar atrophy of the brain", "dementia in Pick's disease", "Lobar Atrophy of the Brain", "Dementia in Pick's disease", "Circumscribed cerebral atrophy", "disease (or disorder); brain, Pick", "Brain Atrophy, Circumscribed Lobar", "Circumscribed Lobar Atrophy of the Brain", "Dementia with Lobar Atrophy and Neuronal Cytoplasmic Inclusions", "DEMENTIA WITH LOBAR ATROPHY AND NEURONAL CYTOPLASMIC INCLUSIONS", "dementia with lobar atrophy and neuronal cytoplasmic inclusions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pick disease", "shortest_name_length": 12}
{"curie": "UMLS:C0677704", "names": ["Stage II Diffuse Small Cleaved Cell Lymphoma", "noncontiguous stage II adult diffuse small cleaved cell lymphoma", "Non-Contiguous Stage II Adult Diffuse Small Cleaved Cell Lymphoma", "Stage II Non-Contiguous Adult Diffuse Small Cleaved Cell Lymphoma", "non-contiguous stage II adult diffuse small cleaved cell lymphoma", "Non-Contiguous Adult Diffuse Small Cleaved Cell Lymphoma Stage II", "non-contiguous adult diffuse small cleaved cell lymphoma stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Non-Contiguous Adult Diffuse Small Cleaved Cell Lymphoma", "shortest_name_length": 44}
{"curie": "UMLS:C4525301", "names": ["Gallbladder cancer", "Stage IIB Gallbladder Cancer", "stage IIB gallbladder cancer", "stage IIB gallbladder cancer AJCC v8", "Stage IIB Gallbladder Cancer AJCC v8", "stage IIB gallbladder carcinoma AJCC v8", "Stage IIB Gallbladder Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Gallbladder Cancer AJCC v8", "shortest_name_length": 18}
{"curie": "MONDO:0003848", "names": ["Ectopic thymus", "Ectopic Thymus", "ectopic thymus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectopic thymus", "shortest_name_length": 14}
{"curie": "UMLS:C4744377", "names": ["Sellar Solitary Fibrous Tumor", "Sellar Solitary Fibrous Tumor/Hemangiopericytoma", "Sellar Hemangiopericytoma/ Solitary Fibrous Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sellar Solitary Fibrous Tumor", "shortest_name_length": 29}
{"curie": "MONDO:0003853", "names": ["Bartholin Gland Adenocarcinoma", "Bartholin gland adenocarcinoma", "BARTHOLIN GLAND, ADENOCARCINOMA", "Bartholin's Gland Adenocarcinoma", "Bartholin's gland adenocarcinoma", "Adenocarcinoma of Bartholin's Gland", "adenocarcinoma of bartholin's gland", "adenocarcinoma of Bartholin's gland", "major vestibular gland adenocarcinoma", "BARTHOLIN GLAND CANCER, ADENOCARCINOMA", "Adenocarcinoma of the Bartholin's Gland", "adenocarcinoma of the Bartholin's gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bartholin gland adenocarcinoma", "shortest_name_length": 30}
{"curie": "UMLS:C2981397", "names": ["Stage IV Appendix Carcinoid Tumor", "Stage IV Appendix Neuroendocrine Tumor", "Stage IV Appendix Carcinoid Tumor AJCC v7", "Stage IV Appendix Neuroendocrine Tumor AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Appendix Neuroendocrine Tumor AJCC v7", "shortest_name_length": 33}
{"curie": "MONDO:0030313", "names": ["IIAE10", "HERPES SIMPLEX ENCEPHALITIS, SUSCEPTIBILITY TO, 7", "herpes simplex encephalitis, susceptibility to, 7", "encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 10", "ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 10", "shortest_name_length": 6}
{"curie": "MONDO:0017773", "names": ["low hdl", "Low HDL", "hdl low", "HDL low", "Decreased HDL", "HDL decreased", "HDL DECREASED", "low hdl cholesterol", "low cholesterol hdl", "CHOLESTEROL HDL LOW", "Low HDL-cholesterol", "Hypoalphalipoproteinemia", "hypoalphalipoproteinemia", "Hypoalphalipoproteinaemia", "Decreased HDL cholesterol", "Hypoalphalipoproteinemias", "HDL cholesterol decreased", "HDL Cholesterol, Low Serum", "Hypo alpha Lipoproteinemia", "Hypo alpha Lipoproteinemias", "alpha Lipoproteinemia, Hypo", "Lipoproteinemia, Hypo alpha", "low high density lipoprotein", "high low density lipoprotein", "Lipoproteinemias, Hypo alpha", "High-density lipoid deficiency", "Decreased serum HDL cholesterol", "High density lipoprotein decrease", "HIGH DENSITY LIPOPROTEIN DECREASE", "HIGH DENSITY LIPOPROTEIN DECREASED", "High density lipoprotein decreased", "Hypoalphalipoproteinemia (disorder)", "Decreased HDL cholesterol concentration", "High density lipoprotein cholesterol low", "Low high-density lipoprotein cholesterol", "High density lipoprotein cholesterol decreased", "Decreased circulating high-density lipoprotein levels", "Decreased circulating high-density lipoprotein cholesterol"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypoalphalipoproteinemia", "shortest_name_length": 7}
{"curie": "MONDO:0017452", "names": ["short toes", "Brachydactyly of toes", "pes non-syndromic brachydactyly", "Brachydactyly of toes (disorder)", "non-syndromic brachydactyly of pes", "non-syndromic brachydactyly of toes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-syndromic brachydactyly of toes", "shortest_name_length": 10}
{"curie": "MONDO:0800028", "names": ["FDFM", "DSKOD", "ADCY5-related dyskinesia", "Familial dyskinesia and facial myokymia", "Dyskinesia, Familial, with Facial Myokymia", "DYSKINESIA, FAMILIAL, WITH FACIAL MYOKYMIA", "dyskinesia, familial, with facial myokymia", "FDFM - familial dyskinesia and facial myokymia", "Familial dyskinesia and facial myokymia (disorder)", "DYSKINESIA WITH OROFACIAL INVOLVEMENT, AUTOSOMAL DOMINANT", "dyskinesia with orofacial involvement, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyskinesia with orofacial involvement, autosomal dominant", "shortest_name_length": 4}
{"curie": "UMLS:C0856148", "names": ["Porphyria aggravated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Porphyria aggravated", "shortest_name_length": 20}
{"curie": "EFO:0009522", "names": ["disturbance of skin sensation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disturbance of skin sensation", "shortest_name_length": 29}
{"curie": "MONDO:0013099", "names": ["genetic hypopituitarism", "familial hypopituitarism", "familial congenital hypopituitarism", "Familial congenital hypopituitarism", "pituitary hormone deficiency, combined", "Combined pituitary hormone deficiency genetic form", "Multiple pituitary hormone deficiency genetic form", "combined pituitary hormone deficiencies, genetic form", "multiple pituitary hormone deficiencies, genetic forms", "Multiple pituitary hormone deficiencies, genetic forms", "combined pituitary hormone deficiencies, genetic forms", "Combined pituitary hormone deficiencies, genetic forms", "Combined pituitary hormone deficiency genetic form (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined pituitary hormone deficiencies, genetic form", "shortest_name_length": 23}
{"curie": "UMLS:C5420046", "names": ["Sinonasal Undifferentiated Pleomorphic Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Undifferentiated Pleomorphic Sarcoma", "shortest_name_length": 46}
{"curie": "MONDO:0010220", "names": ["YOUNG SYNDROME", "Young Syndrome", "young syndrome", "Young syndrome", "Young's syndrome", "Young's syndrome (disorder)", "Barry Perkins Young syndrome", "Barry-Perkins-Young syndrome", "BARRY-PERKINS-YOUNG SYNDROME", "Somatotropic hormone syndrome", "Sinusitis-infertility syndrome", "sinusitis-infertility syndrome", "SINUSITIS-INFERTILITY SYNDROME", "Azoospermia sinopulmonary infections", "Azoospermia-sinopulmonary infections syndrome", "azoospermia-sinopulmonary infections syndrome", "azoospermia obstructive and chronic sinopulmonary infections", "Azoospermia, obstructive and chronic sinopulmonary infections", "azoospermia, obstructive, and chronic sinopulmonary infections", "Azoospermia, obstructive, and chronic sinopulmonary infections", "AZOOSPERMIA, OBSTRUCTIVE, AND CHRONIC SINOPULMONARY INFECTIONS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Young syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C2983569", "names": ["Renal Cell Cancer by AJCC v6 Stage", "Renal Cell Carcinoma by AJCC v6 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal Cell Cancer by AJCC v6 Stage", "shortest_name_length": 34}
{"curie": "UMLS:C3899978", "names": ["BCLC Stage C Hepatocellular Cancer", "BCLC Stage C Adult Hepatocellular Carcinoma", "Barcelona Clinic Liver Cancer Stage C Adult Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "BCLC Stage C Adult Hepatocellular Carcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0100468", "names": ["Becker disease", "Batten-Turner congenital myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Batten-Turner congenital myopathy", "shortest_name_length": 14}
{"curie": "MONDO:0018982", "names": ["NPC", "Type C Niemann-Pick Disease", "niemann-pick type c disease", "Niemann-Pick Type C Disease", "Niemann Pick Type C Disease", "Niemann Pick Disease Type C", "niemann-pick disease type c", "Niemann-Pick disease type C", "Niemann-Pick Disease Type C", "NIEMANN-PICK DISEASE, TYPE C", "Niemann-Pick disease, type C", "Niemann Pick Disease, Type C", "Niemann-Pick Disease, Type C", "Niemann Pick's Disease Type C", "Niemann-Pick's Disease Type C", "Supraoptic vertical ophthalmoplegia", "Niemann-Pick disease, type C (disorder)", "Niemann-Pick disease type C (diagnosis)", "NIEMANN-PICK DISEASE, CHRONIC NEURONOPATHIC FORM", "Niemann Pick Disease, Chronic Neuronopathic Form", "Niemann-Pick Disease, Chronic Neuronopathic Form", "Niemann-Pick Disease without Sphingomyelinase Deficiency", "Niemann Pick Disease without Sphingomyelinase Deficiency", "NIEMANN-PICK DISEASE WITHOUT SPHINGOMYELINASE DEFICIENCY", "Niemann Pick Disease with Cholesterol Esterification Block", "Niemann-Pick Disease with Cholesterol Esterification Block", "NIEMANN-PICK DISEASE WITH CHOLESTEROL ESTERIFICATION BLOCK", "Neurovisceral Storage Disease with Vertical Supranuclear Ophthalmoplegia", "NEUROVISCERAL STORAGE DISEASE WITH VERTICAL SUPRANUCLEAR OPHTHALMOPLEGIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Niemann-Pick disease type C", "shortest_name_length": 3}
{"curie": "MONDO:0020660", "names": ["Osteoblastic sarcoma", "Osteoblastic Osteosarcoma", "Osteoblastic osteosarcoma", "osteoblastic osteosarcoma", "osteosarcoma, osteoblastic", "osteoblastic osteogenic sarcoma", "osteogenic sarcoma, osteoblastic", "sarcoma, osteogenic osteoblastic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteoblastic osteosarcoma", "shortest_name_length": 20}
{"curie": "UMLS:C0342155", "names": ["Congenital hypothyroidism with ectopic thyroid", "Congenital Hypothyroidism with Ectopic Thyroid", "Congenital hypothyroidism with ectopic thyroid (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital hypothyroidism with ectopic thyroid", "shortest_name_length": 46}
{"curie": "MONDO:0011374", "names": ["ARH", "ARH1", "ARH2", "FHCL4", "FHCB2", "FCHL4", "FHCB1", "ARH2, FORMERLY", "ARH1, FORMERLY", "FHCB2, FORMERLY", "FHCB1, FORMERLY", "FHCB2, formerly", "FHCB1, formerly", "Hypercholesterolemia, Familial, 4", "hypercholesterolemia, familial, 4", "HYPERCHOLESTEROLEMIA, FAMILIAL, 4", "Autosomal Recessive Hypercholesterolemia", "autosomal recessive hypercholesterolemia", "Autosomal Recessive Hypercholesterolemias", "HYPERCHOLESTEROLEMIA, AUTOSOMAL RECESSIVE", "hypercholesterolemia, autosomal recessive", "Hypercholesterolemia, Autosomal Recessive", "Recessive Hypercholesterolemia, Autosomal", "autosomal recessive hypercholesterolemia 2", "autosomal recessive hypercholesterolemia 1", "hypercholesterolemia, autosomal recessive, 2", "hypercholesterolemia, autosomal recessive, 1", "familial autosomal recessive hypercholesterolemia", "HYPERCHOLESTEROLEMIA, AUTOSOMAL RECESSIVE, 1, FORMERLY", "hypercholesterolemia, autosomal recessive, 1, formerly", "hypercholesterolemia, autosomal recessive, 2, formerly", "HYPERCHOLESTEROLEMIA, AUTOSOMAL RECESSIVE, 2, FORMERLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypercholesterolemia, familial, 4", "shortest_name_length": 3}
{"curie": "UMLS:C1275403", "names": ["Regressed germ cell tumor", "Burnt-Out Germ Cell Tumor", "Burnt out germ cell tumor", "Regressed germ cell tumour", "Burnt out germ cell tumour", "Regressed Testicular Germ Cell Tumor", "Regressed germ cell tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Regressed germ cell tumor", "shortest_name_length": 25}
{"curie": "UMLS:C5206596", "names": ["Paratesticular Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paratesticular Liposarcoma", "shortest_name_length": 26}
{"curie": "MONDO:0019806", "names": ["PPA", "PPAOS", "Mesulam Syndrome", "Mesulam syndrome", "Syndrome, Mesulam", "Mesulam's Syndrome", "Syndrome, Mesulam's", "primary progressive aphasia", "Primary progressive aphasia", "Primary Progressive Aphasia", "progressive primary aphasia", "Primary Progressive Aphasias", "Progressive Aphasia, Primary", "Aphasia, Primary Progressive", "APHASIA, PRIMARY PROGRESSIVE", "Aphasias, Primary Progressive", "Progressive Aphasias, Primary", "primary progressive aphasia syndrome", "Primary progressive apraxia of speech", "Primary Progressive Aphasia (disorder)", "Primary progressive apraxia of speech (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary progressive aphasia", "shortest_name_length": 3}
{"curie": "MONDO:0019586", "names": ["X-linked deafness", "X-linked nonsyndromic deafness", "nonsyndromic deafness, X-linked", "X-linked nonsyndromic hearing loss", "X-linked nonsyndromic genetic deafness", "nonsyndromic genetic deafness, X-linked", "X-linked isolated neurosensory deafness type DFN", "X-linked isolated sensorineural deafness type DFN", "X-linked isolated neurosensory hearing loss type DFN", "X-linked non-syndromic neurosensory deafness type DFN", "X-linked isolated sensorineural hearing loss type DFN", "X-linked non-syndromic sensorineural deafness type DFN", "X-linked non-syndromic neurosensory hearing loss type DFN", "X-linked non-syndromic sensorineural hearing loss type DFN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked nonsyndromic hearing loss", "shortest_name_length": 17}
{"curie": "UMLS:C1333835", "names": ["Grade 2 Clear Cell Renal Cell Carcinoma", "Grade 2 Conventional (Clear Cell) Renal Cell Carcinoma", "G2 Nuclei slightly irregular, approximately 15 um; nucleoli evident"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade 2 Clear Cell Renal Cell Carcinoma", "shortest_name_length": 39}
{"curie": "MONDO:0010882", "names": ["aphalangy-syndactyly-microcephaly syndrome", "Aphalangia partial with syndactyly and duplication of metatarsal IV", "Aphalangia, partial, with syndactyly and Duplication of metatarsal 4", "Aphalangia, Partial, with Syndactyly and Duplication of Metatarsal IV", "APHALANGIA, PARTIAL, WITH SYNDACTYLY AND DUPLICATION OF METATARSAL IV", "APHALANGIA, partial, with syndactyly and DUPLICATION of metatarsal IV", "Aphalangia, partial, with syndactyly and Duplication of metatarsal type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aphalangy-syndactyly-microcephaly syndrome", "shortest_name_length": 42}
{"curie": "MONDO:0008430", "names": ["skeletal dysplasia with delayed epiphyseal and carpal bone ossification", "Skeletal Dysplasia With Delayed Epiphyseal And Carpal Bone Ossification", "SKELETAL DYSPLASIA WITH DELAYED EPIPHYSEAL AND CARPAL BONE OSSIFICATION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skeletal dysplasia with delayed epiphyseal and carpal bone ossification", "shortest_name_length": 71}
{"curie": "UMLS:C2217035", "names": ["Stage IIA Colon Cancer", "Stage IIA Colon Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Colon Cancer AJCC v7", "shortest_name_length": 22}
{"curie": "MONDO:0014287", "names": ["SRTD11", "SHORT-RIB THORACIC DYSPLASIA 11 WITH OR WITHOUT POLYDACTYLY", "short-rib thoracic dysplasia 11 with or without polydactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short-rib thoracic dysplasia 11 with or without polydactyly", "shortest_name_length": 6}
{"curie": "MONDO:0011200", "names": ["DYT7", "torsion dystonia 7", "Torsion dystonia 7", "dystonia-7, torsion", "dystonia 7, torsion", "DYSTONIA 7, TORSION", "Dystonia 7, Torsion", "torsion dystonia type 7", "Cervical Dystonia, Primary", "Dystonia, Primary Cervical", "CERVICAL DYSTONIA, PRIMARY", "cervical dystonia, primary", "DYSTONIA 7, TORSION (disorder)", "Torsion dystonia, focal adult-onset", "TORSION DYSTONIA, FOCAL ADULT-ONSET", "torsion dystonia, focal adult-onset", "Primary adult-onset torsion dystonia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "torsion dystonia 7", "shortest_name_length": 4}
{"curie": "UMLS:C1336142", "names": ["Stage IB Ovarian Germ Cell Tumor", "Stage IB Ovarian Germ Cell Tumor AJCC v7", "Stage IB Ovarian Germ Cell Tumor AJCC v6", "FIGO Stage IB Malignant Ovarian Germ Cell Tumor", "Stage IB Ovarian Germ Cell Tumor AJCC v6 and v7", "FIGO Stage IB Malignant Germ Cell Tumor of Ovary", "FIGO Stage IB Malignant Ovarian Germ Cell Neoplasm", "FIGO Stage IB Malignant Germ Cell Neoplasm of Ovary", "FIGO Stage IB Malignant Germ Cell Tumor of the Ovary", "FIGO Stage IB Malignant Germ Cell Neoplasm of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Ovarian Germ Cell Tumor AJCC v6 and v7", "shortest_name_length": 32}
{"curie": "UMLS:C5420149", "names": ["Refractory Microsatellite Stable Colorectal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Microsatellite Stable Colorectal Carcinoma", "shortest_name_length": 53}
{"curie": "MONDO:0014437", "names": ["BBS9", "BARDET-BIEDL SYNDROME 9", "Bardet-Biedl Syndrome 9", "Bardet-Biedl syndrome 9", "BBS9 Bardet-Biedl syndrome", "Bardet-Biedl syndrome type 9", "Bardet-Biedl syndrome caused by mutation in BBS9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bardet-Biedl syndrome 9", "shortest_name_length": 4}
{"curie": "UMLS:C1533591", "names": ["CALCIFIC", "Calcification", "mineralization", "Mineralization", "CALCIUM DEPOSIT", "Deposit calcium", "DEPOSIT CALCIUM", "CALCIUM DEPOSITS", "Calcium deposits", "Calcification, NOS", "Mineralization, NOS", "Calcium Depositions", "Deposition, calcium", "Calcium deposition, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Calcification", "shortest_name_length": 8}
{"curie": "MONDO:0020756", "names": ["FHM", "MHP1", "FHM1", "Sporadic Hemiplegic Migraine", "migraine, sporadic hemiplegic", "Migraine, Sporadic Hemiplegic", "MIGRAINE, SPORADIC HEMIPLEGIC", "familial hemiplegic migraine 1", "Familial Hemiplegic Migraine-1", "migraine, familial hemiplegic, 1", "MIGRAINE, FAMILIAL HEMIPLEGIC, 1", "Migraine, Familial Hemiplegic, 1", "familial hemiplegic migraine type 1", "Hemiplegic migraine, familial type 1", "hemiplegic migraine, familial type 1", "migraine, familial hemiplegic, type 1", "familial hemiplegic migraine1 with progressive cerebellar ataxia", "migraine, familial hemiplegic 1, with progressive cerebellar ataxia", "Migraine, familial hemiplegic 1, with progressive cerebellar ataxia", "MIGRAINE, FAMILIAL HEMIPLEGIC 1, WITH PROGRESSIVE CEREBELLAR ATAXIA", "migraine, familial hemiplegic, 1, with progressive cerebellar ataxia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "migraine, familial hemiplegic, 1", "shortest_name_length": 3}
{"curie": "MONDO:0021026", "names": ["genetic epidermal appendage anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genetic epidermal appendage anomaly", "shortest_name_length": 35}
{"curie": "MONDO:0000243", "names": ["ectothrix infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectothrix infectious disease", "shortest_name_length": 28}
{"curie": "MONDO:0001577", "names": ["RSV", "infection rsv", "RSV Infection", "rsv infection", "RSV Infections", "respiratory syncytial virus", "Respiratory Syncytial Virus Infection", "respiratory syncytial virus infection", "Respiratory syncytial virus infection", "Respiratory Syncytial Virus Infections", "Infections, Respiratory Syncytial Virus", "Respiratory syncytial virus infection NOS", "Respiratory syncytial virus infection, NOS", "Human respiratory syncytial virus infection", "RSV - Respiratory syncytial virus infection", "RESPIRATORY TRACT, SYNCYTIAL VIRUS INFECTION", "infections, Human respiratory syncytial virus", "respiratory syncytial virus infectious disease", "Respiratory syncytial virus infection (disorder)", "respiratory syncytial virus infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "respiratory syncytial virus infectious disease", "shortest_name_length": 3}
{"curie": "MONDO:0044685", "names": ["autoimmune/inflammatory optic neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune/inflammatory optic neuropathy", "shortest_name_length": 40}
{"curie": "MONDO:0004071", "names": ["Cerebral Astrocytoma", "cerebral astrocytoma", "Childhood Cerebral Astrocytoma", "pediatric cerebral astrocytoma", "Pediatric Cerebral Astrocytoma", "childhood cerebral astrocytoma", "Childhood Cerebral Astrocytomas", "cerebral astrocytoma, childhood", "Cerebral Astrocytoma, Childhood", "astrocytoma, childhood cerebral", "Astrocytoma, Childhood Cerebral", "astrocytoma, pediatric cerebral", "childhood astrocytoma of cerebrum", "pediatric astrocytoma of cerebrum", "Pediatric Astrocytoma of Cerebrum", "Childhood Astrocytoma of Cerebrum", "pediatric astrocytoma of Cerebrum", "telencephalon juvenile astrocytoma", "pediatric supratentorial astrocytoma", "childhood supratentorial astrocytoma", "childhood astrocytoma of the cerebrum", "pediatric astrocytoma of the cerebrum", "Pediatric Astrocytoma of the Cerebrum", "supratentorial astrocytoma, childhood", "Childhood Astrocytoma of the Cerebrum", "telencephalon childhood astrocytic tumor", "CNS tumor, pediatric cerebral astrocytoma", "CNS tumor, childhood cerebral astrocytoma", "childhood CNS tumor, cerebral astrocytoma", "pediatric CNS tumor, cerebral astrocytoma", "brain tumor, childhood cerebral astrocytoma", "childhood brain tumor, cerebral astrocytoma", "brain tumor, pediatric cerebral astrocytoma", "childhood astrocytic tumor of telencephalon", "pediatric brain tumor, cerebral astrocytoma", "childhood cerebral astrocytoma/malignant glioma", "pediatric cerebral astrocytoma/malignant glioma", "cerebral astrocytoma/malignant glioma, childhood", "cerebral astrocytoma/malignant glioma, pediatric", "central nervous system tumor, cerebral astrocytoma, childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood cerebral astrocytoma", "shortest_name_length": 20}
{"curie": "MONDO:0005693", "names": ["Polyneuritis equi", "Lumbosacral syndrome", "lumbosacral syndrome", "Cauda equina syndrome", "CAUDA EQUINA SYNDROME", "syndrome cauda equina", "Cauda Equina Syndrome", "cauda equina syndrome", "Cauda equina neuritis", "syndrome; cauda equina", "cauda equina; syndrome", "Cauda Equina Syndromes", "Cauda equina syndrome, NOS", "cauda equina syndromic disease", "Cauda equina syndrome (disorder)", "cauda equina syndrome (diagnosis)", "syndromic disease of cauda equina"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cauda equina syndrome", "shortest_name_length": 17}
{"curie": "MONDO:0012368", "names": ["ACY1D", "ACY1 deficiency", "aminoacylase 1 deficiency", "Aminoacylase 1 deficiency", "AMINOACYLASE 1 DEFICIENCY", "Deficiency of aminoacylase 1", "Deficiency of aminoacylase 1 (disorder)", "deficiency of the aminoacylase-1 enzyme", "Deficiency of the aminoacylase-1 enzyme", "N-acyl-L-amino acid amidohydrolase deficiency", "Neurological conditions associated with aminoacylase 1 deficiency", "neurological conditions associated with aminoacylase 1 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aminoacylase 1 deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C4553787", "names": ["Stage IV Renal Pelvis and Ureter Cancer", "Stage IV Renal Pelvis and Ureter Cancer AJCC v8", "stage IV renal pelvis and ureter cancer AJCC v8", "Stage IV Renal Pelvis and Ureter Urothelial Carcinoma AJCC v8", "stage IV renal pelvis and ureter urothelial carcinoma AJCC v8", "stage IV transitional cell cancer of the renal pelvis and ureter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Renal Pelvis and Ureter Cancer AJCC v8", "shortest_name_length": 39}
{"curie": "MONDO:0006596", "names": ["Photoallergic eczema", "photoallergic eczema", "photocontact dermatitis", "Photocontact Dermatitis", "Photocontact dermatitis", "photoallergic dermatitis", "Photoallergic dermatitis", "Dermatitis, Photocontact", "Photoallergic Dermatitis", "Photocontact Dermatitides", "Dermatitis, Photoallergic", "Dermatitides, Photocontact", "Photoallergic Dermatitides", "Dermatitides, Photoallergic", "Allergic photocontact eczema", "Photoallergic dermatitis, NOS", "photoallergic contact dermatitis", "Photoallergic Contact Dermatitis", "Photoallergic contact dermatitis", "Dermatitis, Photoallergic Contact", "Photosensitive Contact Dermatitis", "Contact Dermatitis, Photoallergic", "Contact Dermatitis, Photosensitive", "Dermatitis, Contact, Photoallergic", "Dermatitis, Photosensitive Contact", "Photoallergic Contact Dermatitides", "Photoallergic dermatitis (disorder)", "Dermatitis, Contact, Photosensitive", "Contact Dermatitides, Photoallergic", "Dermatitides, Photoallergic Contact", "Photosensitive Contact Dermatitides", "Dermatitides, Photosensitive Contact", "Contact Dermatitides, Photosensitive", "Photoallergic contact dermatitis, NOS", "photoallergic contact dermatitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "photoallergic dermatitis", "shortest_name_length": 20}
{"curie": "MONDO:0018065", "names": ["isolated trigonocephaly", "nonsyndromic trigonocephaly", "non-syndromic metopic craniosynostosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated trigonocephaly", "shortest_name_length": 23}
{"curie": "UMLS:C0333258", "names": ["lymphorrhea", "Lymphorrhea", "Lymphorrhoea", "Extravasation of lymph", "Extravasation of lymph (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extravasation of lymph", "shortest_name_length": 11}
{"curie": "MONDO:0024548", "names": ["PSS", "PSS1", "PSS type B", "Deciduous Skin", "DECIDUOUS SKIN", "Deciduous skin", "deciduous skin", "Peeling skin disease", "Peeling Skin Syndrome", "PEELING SKIN SYNDROME", "Peeling skin syndrome", "PEELING SKIN SYNDROME 1", "peeling skin syndrome 1", "Peeling skin syndrome 1", "Idiopathic deciduous skin", "CDSN peeling skin syndrome", "peeling skin syndrome type B", "Keratosis exfoliativa congenita", "Hereditary skin peeling syndrome", "Keratolysis Exfoliativa Congenita", "keratolysis exfoliativa congenita", "generalized deciduous skin type B", "KERATOLYSIS EXFOLIATIVA CONGENITA", "inflammatory peeling skin syndrome", "generalized peeling skin syndrome type B", "Familial continuous skin peeling syndrome", "Hereditary skin peeling syndrome (disorder)", "Skin Peeling, Familial Continuous Generalized", "SKIN PEELING, FAMILIAL CONTINUOUS GENERALIZED", "skin peeling, familial continuous generalized", "peeling skin syndrome caused by mutation in CDSN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peeling skin syndrome 1", "shortest_name_length": 3}
{"curie": "UMLS:C0854861", "names": ["Stage II T-Lymphoblastic Leukemia/Lymphoma", "Stage II T Lymphoblastic Leukemia/Lymphoma", "Precursor T-lymphoblastic lymphoma/leukemia stage II", "Precursor T-Lymphoblastic Lymphoma/Leukemia Stage II", "Stage II Precursor T-Lymphoblastic Lymphoma/Leukemia", "Precursor T-lymphoblastic lymphoma/leukaemia stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Precursor T-lymphoblastic lymphoma/leukemia stage II", "shortest_name_length": 42}
{"curie": "UMLS:C1394290", "names": ["Cyanotic heart disease", "cyanotic; heart disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cyanotic heart disease", "shortest_name_length": 22}
{"curie": "UMLS:C4329625", "names": ["Central Nervous System Anaplastic Large Cell Lymphoma, ALK-Negative", "Primary Central Nervous System Anaplastic Large Cell Lymphoma, ALK-Negative"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Anaplastic Large Cell Lymphoma, ALK-Negative", "shortest_name_length": 67}
{"curie": "MONDO:0023094", "names": ["ocular ochronosis", "pseudo-ochronosis", "ochronosis, acquired", "exogenous ochronosis", "Alkaptonuric ochronosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exogenous ochronosis", "shortest_name_length": 17}
{"curie": "UMLS:C5420785", "names": ["Ipsilateral Nodule", "IPSILATERAL_NODULES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ipsilateral Nodule", "shortest_name_length": 18}
{"curie": "MONDO:0023595", "names": ["MYOTONIC dystrophy CONGEN", "congenital myotonic dystrophy", "Congenital Myotonic Dystrophy", "Congenital Myotonic dystrophy", "Congenital myotonic dystrophy", "dystrophy, Congenital Myotonic", "Myotonic dystrophy, Congenital", "Myotonic Dystrophy, Congenital", "Dystrophy, Congenital Myotonic", "Congenital Myotonic Dystrophies", "Congenital Myotonic dystrophies", "Myotonic Dystrophies, Congenital", "Dystrophies, Congenital Myotonic", "Myotonic dystrophies, Congenital", "dystrophies, Congenital Myotonic", "Congenital myotonic dystrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myotonic dystrophy", "shortest_name_length": 25}
{"curie": "MONDO:0014750", "names": ["CILD33", "primary ciliary dyskinesia 33", "ciliary dyskinesia, primary, 33", "GAS8 primary ciliary dyskinesia", "CILIARY DYSKINESIA, PRIMARY, 33", "primary ciliary dyskinesia type 33", "ciliary dyskinesia, primary, type 33", "primary ciliary dyskinesia 33 without situs inversus", "primary ciliary dyskinesia caused by mutation in GAS8", "CILIARY DYSKINESIA, PRIMARY, 33, WITHOUT SITUS INVERSUS", "ciliary dyskinesia, primary, 33, without situs inversus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia 33", "shortest_name_length": 6}
{"curie": "MONDO:0007221", "names": ["BDC", "Type C brachydactyly", "Brachydactyly type C", "brachydactyly type C", "Brachydactyly, Type C", "brachydactyly, type C", "BRACHYDACTYLY, TYPE C", "brachydactyly Haws type", "Brachydactyly Haws type", "Brachydactyly, Haws Type", "BRACHYDACTYLY, HAWS TYPE", "brachydactyly, Haws type", "Brachydactyly syndrome type C", "Brachydactyly syndrome type C (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly type C", "shortest_name_length": 3}
{"curie": "MONDO:0007612", "names": ["GFD", "Jones syndrome", "JONES SYNDROME", "Fibromatosis gingival progressive deafness", "Gingival fibromatosis with progressive deafness", "gingival fibromatosis with progressive deafness", "FIBROMATOSIS, GINGIVAL, WITH PROGRESSIVE DEAFNESS", "fibromatosis, gingival, with progressive deafness", "Fibromatosis, Gingival, With Progressive Deafness", "gingival fibromatosis-progressive deafness syndrome", "Gingival fibromatosis-progressive deafness syndrome", "GINGIVAL FIBROMATOSIS WITH SENSORINEURAL HEARING LOSS", "gingival fibromatosis with sensorineural hearing loss", "Gingival fibromatosis with sensorineural hearing loss", "Gingival fibromatosis-progressive hearing loss syndrome", "Gingival fibromatosis with progressive deafness syndrome", "familial gingival fibromatosis associated with progressive deafness", "Gingival fibromatosis with progressive deafness syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gingival fibromatosis-progressive deafness syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0023388", "names": ["pityriasis rotunda", "Pityriasis rotunda", "pityriasis; rotunda", "rotunda; pityriasis", "Pityriasis rotunda (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pityriasis rotunda", "shortest_name_length": 18}
{"curie": "UMLS:C1333768", "names": ["Gastric GIST", "GIST of Stomach", "GIST of the Stomach", "Stomach Digestive Stromal Tumor", "Gastric Digestive Stromal Tumor", "Gastric Digestive Stromal Neoplasm", "Digestive Stromal Tumor of Stomach", "Stomach Digestive Stromal Neoplasm", "Digestive Stromal Neoplasm of Stomach", "Gastric Gastrointestinal Stromal Tumor", "Digestive Stromal Tumor of the Stomach", "Digestive Stromal Neoplasm of the Stomach", "Gastrointestinal Stromal Tumor of Stomach", "Gastrointestinal stromal tumor of stomach", "Gastrointestinal stromal tumour of stomach", "Gastrointestinal Stromal Neoplasm of Stomach", "gastrointestinal stromal neoplasm of stomach", "Gastrointestinal Stromal Tumor of the Stomach", "Gastrointestinal Stromal Neoplasm of the Stomach", "neoplasm gastrointestinal tract stromal of stomach", "Gastrointestinal stromal tumor of stomach (disorder)", "Gastric (Stomach) Gastrointestinal Stromal Tumor (GIST)", "gastrointestinal stromal neoplasm of stomach (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Gastrointestinal Stromal Tumor", "shortest_name_length": 12}
{"curie": "MONDO:0032741", "names": ["NEDISHM", "NEURODEVELOPMENTAL DISORDER WITH IMPAIRED SPEECH AND HYPERKINETIC MOVEMENTS", "neurodevelopmental disorder with impaired speech and hyperkinetic movements"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with impaired speech and hyperkinetic movements", "shortest_name_length": 7}
{"curie": "UMLS:C5418828", "names": ["Metastatic Thyroid Gland Anaplastic Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Thyroid Gland Anaplastic Carcinoma", "shortest_name_length": 45}
{"curie": "MONDO:0010189", "names": ["vitiligo, progressive, with mental retardation and urethral duplication", "Vitiligo, Progressive, with Mental Retardation and Urethral Duplication", "VITILIGO, PROGRESSIVE, WITH MENTAL RETARDATION AND URETHRAL DUPLICATION", "vitiligo, progressive, with intellectual disability and urethral duplication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitiligo, progressive, with intellectual disability and urethral duplication", "shortest_name_length": 71}
{"curie": "MONDO:0003915", "names": ["thymoma type B2", "type B2 thymoma", "Thymoma Type B2", "Cortical Thymoma", "cortical thymoma", "Thymoma, cortical", "thymoma, cortical", "Thymoma, type B2, NOS", "polygonal cell thymoma", "Polygonal cell Thymoma", "Polygonal Cell Thymoma", "type B2 thymoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cortical thymoma", "shortest_name_length": 15}
{"curie": "MONDO:0043096", "names": ["fetus anideus", "Fetus anideus", "Foetus anideus", "Amorphus globosus", "amorphus globosus", "Amorphous globosus", "amorphous globosus", "holoacardius amorphus", "Holoacardius amorphus", "Holoacardius amorphus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "holoacardius amorphus", "shortest_name_length": 13}
{"curie": "UMLS:C4553577", "names": ["Stage III Thyroid Gland Medullary Cancer", "Stage III Thyroid Gland Medullary Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Thyroid Gland Medullary Carcinoma AJCC v8", "shortest_name_length": 40}
{"curie": "MONDO:0007833", "names": ["iris pigment layer, cleavage of", "IRIS PIGMENT LAYER, CLEAVAGE OF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "iris pigment layer, cleavage of", "shortest_name_length": 31}
{"curie": "MONDO:0013403", "names": ["HTX4", "ACVR2B visceral heterotaxy", "heterotaxy, visceral, 4, autosomal", "HETEROTAXY, VISCERAL, 4, AUTOSOMAL", "visceral heterotaxy caused by mutation in ACVR2B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heterotaxy, visceral, 4, autosomal", "shortest_name_length": 4}
{"curie": "MONDO:0009365", "names": ["HLS1", "hydrolethalus syndrome", "Hydrolethalus Syndrome 1", "hydrolethalus syndrome 1", "HYDROLETHALUS SYNDROME 1", "HYLS1 hydrolethalus syndrome", "hydrolethalus syndrome type 1", "hydrolethalus syndrome caused by mutation in HYLS1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hydrolethalus syndrome 1", "shortest_name_length": 4}
{"curie": "UMLS:C0399470", "names": ["Buccal mucosa leukoplakia", "leukoplakia of buccal mucosa", "Leukoplakia of buccal mucosa", "Leukoplakia of Buccal Mucosa", "Leucoplakia of buccal mucosa", "Leukoplakia of buccal mucosa (disorder)", "leukoplakia of buccal mucosa (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leukoplakia of buccal mucosa", "shortest_name_length": 25}
{"curie": "MONDO:0013948", "names": ["CGG", "CG12", "PBD10A", "peroxisome biogenesis disorder 10A", "PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER)", "peroxisome biogenesis disorder 10A (Zellweger)", "peroxisome biogenesis disorder, complementation group G", "Peroxisome Biogenesis Disorder, Complementation Group G", "PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP G", "PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 12", "peroxisome biogenesis disorder, complementation group 12", "Peroxisome Biogenesis Disorder, Complementation Group 12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder 10A (Zellweger)", "shortest_name_length": 3}
{"curie": "MONDO:0030457", "names": ["IMD87", "immunodeficiency 87 and autoimmunity", "IMMUNODEFICIENCY 87 AND AUTOIMMUNITY", "immunodeficiency due to DEF6 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 87 and autoimmunity", "shortest_name_length": 5}
{"curie": "UMLS:C0406326", "names": ["Scalp psoriasis", "psoriasis scalp", "scalp psoriasis", "Psoriasis of scalp", "psoriasis of scalp", "Psoriasis of scalp (disorder)", "Psoriasis of scalp (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Psoriasis of scalp", "shortest_name_length": 15}
{"curie": "MONDO:0009852", "names": ["IFD", "Castle's deficiency", "Intrinsic Factor Deficiency", "Intrinsic factor deficiency", "INTRINSIC FACTOR DEFICIENCY", "intrinsic factor deficiency", "intrinsic factor; deficiency", "congenital pernicious anemia", "deficiency; intrinsic factor", "Congenital pernicious anemia", "gastric intrinsic factor deficiency", "Gastric intrinsic factor deficiency", "congenital intrinsic factor deficiency", "hereditary intrinsic factor deficiency", "Congenital intrinsic factor deficiency", "intrinsic factor deficiency; congenital", "congenital; intrinsic factor deficiency", "Congenital deficiency of intrinsic factor", "intrinsic factor, congenital deficiency of", "Congenital intrinsic factor deficiency anemia", "Congenital intrinsic factor deficiency anaemia", "Congenital deficiency of intrinsic factor (disorder)", "congenital pernicious anemia due to defect of intrinsic factor", "pernicious Anemia, congenital, due to defect of intrinsic Factor", "Pernicious Anemia, Congenital, due to Defect of Intrinsic Factor", "PERNICIOUS ANEMIA, CONGENITAL, DUE TO DEFECT OF INTRINSIC FACTOR", "Megaloblastic anemia due to congenital deficiency of intrinsic factor", "Megaloblastic anaemia due to congenital deficiency of intrinsic factor", "Hereditary juvenile megaloblastic anemia due to intrinsic factor deficiency", "hereditary juvenile megaloblastic anemia due to intrinsic factor deficiency", "Megaloblastic anemia due to congenital deficiency of intrinsic factor (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary intrinsic factor deficiency", "shortest_name_length": 3}
{"curie": "MONDO:0009585", "names": ["MCDU", "Ampola syndrome", "disulfiduria, mixed", "DISULFIDURIA, MIXED", "Disulfiduria, Mixed", "mercaptolactate-cysteine disulfiduria", "Mercaptolactate-Cysteine Disulfiduria", "MERCAPTOLACTATE-CYSTEINE DISULFIDURIA", "B-mercaptolactate-cysteine disulfiduria", "beta-mercaptolactate-cysteine disulfiduria", "Beta-mercaptolactate cysteine disulfiduria", "mercaptolactate-cysteine disulfiduria (MCDU)", "3-mercaptopyruvate sulfurtransferase deficiency", "Beta-mercaptolactate cysteine disulfiduria (disorder)", "beta-mercaptolactate-cysteine disulfiduria (diagnosis)", "encephalopathy due to beta-mercaptolactate-cysteine disulfiduria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephalopathy due to beta-mercaptolactate-cysteine disulfiduria", "shortest_name_length": 4}
{"curie": "MONDO:0044877", "names": ["PCD", "Subacute cerebellar degeneration", "Paraneoplastic cerebellar ataxia", "Cerebellar ataxia due to neoplasia", "Paraneoplastic Cerebellar Syndrome", "Cerebellar Syndrome, Paraneoplastic", "Paraneoplastic Cerebellar Syndromes", "Cerebellar Syndromes, Paraneoplastic", "Paraneoplastic Cerebellar Degeneration", "paraneoplastic cerebellar degeneration", "Paraneoplastic cerebellar degeneration", "Degeneration, Paraneoplastic Cerebellar", "Cerebellar Degeneration, Paraneoplastic", "Rapidely progressive cerebellar syndrome", "Paraneoplastic cerebellar degeneration (disorder)", "paraneoplastic cerebellar degeneration (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paraneoplastic cerebellar degeneration", "shortest_name_length": 3}
{"curie": "UMLS:C0155943", "names": ["TMJ pain", "arthralgia of TMJ", "temporomandibular joint pain", "Temporomandibular joint pain", "joint pain temporomandibular", "TEMPOROMANDIBULAR JOINT PAIN", "pain in temporomandibular joint", "Temporomandibular joint arthralgia", "arthralgia of temporomandibular joint", "Arthralgia of temporomandibular joint", "Temporomandibular joint pain (finding)", "pain in temporomandibular joint (symptom)", "Arthralgia of temporomandibular joint (disorder)", "arthralgia of temporomandibular joint (diagnosis)", "Temporomandibular joint disorders, arthralgia of temporomandibular joint"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arthralgia of temporomandibular joint", "shortest_name_length": 8}
{"curie": "UMLS:C0162818", "names": ["Papulosquamous Disorder", "papulosquamous disorder", "Disorder, Papulosquamous", "papulosquamous; disorder", "Papulosquamous Disorders", "Papulosquamous disorders", "Papulosquamous dermatosis", "Disorders, Papulosquamous", "papulosquamous; dermatosis", "Papulo-squamous dermatosis", "dermatosis; papulosquamous", "Papulosquamous Skin Disease", "Papulosquamous Skin Diseases", "Disease, Papulosquamous Skin", "Skin Disease, Papulosquamous", "Diseases, Papulosquamous Skin", "Skin Diseases, Papulosquamous", "Papulosquamous dermatosis, NOS", "Papulosquamous disorders (L40-L45)", "papulosquamous disorder (diagnosis)", "Papulosquamous dermatosis (disorder)", "Papulosquamous disorder, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin Diseases, Papulosquamous", "shortest_name_length": 23}
{"curie": "UMLS:C5399767", "names": ["Middle ear effusion", "Middle ear effusion (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Middle ear effusion", "shortest_name_length": 19}
{"curie": "MONDO:0014246", "names": ["FEPS2", "familial episodic pain syndrome 2", "EPISODIC PAIN SYNDROME, FAMILIAL, 2", "episodic pain syndrome, familial, 2", "SCN10A familial episodic pain syndrome", "episodic pain syndrome, familial, type 2", "familial episodic pain syndrome caused by mutation in SCN10A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "episodic pain syndrome, familial, 2", "shortest_name_length": 5}
{"curie": "UMLS:C4744472", "names": ["Chromophobe Renal Cell Carcinoma Associated with Birt-Hogg-Dube Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chromophobe Renal Cell Carcinoma Associated with Birt-Hogg-Dube Syndrome", "shortest_name_length": 72}
{"curie": "MONDO:0015324", "names": ["Karandikar-Maria-Kamble syndrome", "Karandikar Maria Kamble syndrome", "cataract mental retardation anal atresia urinary defects", "Cataract mental retardation anal atresia urinary defects", "cataract intellectual disability anal atresia urinary defects", "congenital cataract with multiple congenital anomalies in a sibship", "Congenital cataract with multiple congenital anomalies in a sibship", "Cataract-intellectual disability-anal atresia-urinary defects syndrome", "cataract-intellectual disability-anal atresia-urinary defects syndrome", "Congenital cataract with intellectual disability and anal atresia and urinary defect syndrome", "Congenital cataract with intellectual disability and anal atresia and urinary defect syndrome (disorder)", "Congenital cataract with intellectual disability and anal atresia and urinary defect syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract-intellectual disability-anal atresia-urinary defects syndrome", "shortest_name_length": 32}
{"curie": "MONDO:0001180", "names": ["bullous keratopathy", "Bullous Keratopathy", "Bullous keratopathy", "bullous; keratopathy", "keratopathy; bullous", "BK - Bullous keratopathy", "Bullous keratopathy (disorder)", "bullous keratopathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bullous keratopathy", "shortest_name_length": 19}
{"curie": "UMLS:C4524643", "names": ["Esophageal Squamous Cell Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Squamous Cell Carcinoma by AJCC v7 Stage", "shortest_name_length": 51}
{"curie": "MONDO:0010560", "names": ["CPX", "cleft palate X-linked", "X-linked cleft palate", "Cleft palate X-linked", "CLEFT PALATE, X-LINKED", "cleft palate, X-linked", "Cleft Palate, X-Linked", "cleft palate with ankyloglossia", "X-linked cleft palate and ankyloglossia", "X-linked cleft palate and ankyloglossia (disorder)", "X-linked cleft palate with or without ankyloglossia", "CLEFT PALATE WITH OR WITHOUT ANKYLOGLOSSIA, X-LINKED", "cleft palate with or without ankyloglossia, X-linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleft palate with or without ankyloglossia, X-linked", "shortest_name_length": 3}
{"curie": "UMLS:C0347602", "names": ["retina injury", "Retinal injury", "retinal injury", "retina; injury", "injury; retina", "injuries retina", "injury of retina", "Injury of retina", "injuries retinal", "Injury of retina (disorder)", "injury of retina (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of retina", "shortest_name_length": 13}
{"curie": "UMLS:C1336183", "names": ["fallopian tube cancer stage IIB", "stage IIB fallopian tube cancer", "Stage IIB Fallopian Tube Cancer", "Fallopian Tube Cancer Stage IIB", "AJCC Stage IIB Fallopian Tube Cancer", "AJCC stage IIB fallopian tube cancer", "Stage IIB Fallopian Tube Cancer AJCC v6", "stage IIB fallopian tube cancer AJCC v7", "Stage IIB Fallopian Tube Cancer AJCC v7", "FIGO stage IIB fallopian tube carcinoma", "stage IIB fallopian tube cancer AJCC v6", "FIGO Stage IIB Fallopian Tube Carcinoma", "FIGO stage IIB carcinoma of fallopian tube", "FIGO Stage IIB Carcinoma of Fallopian Tube", "FIGO stage IIB carcinoma of the fallopian tube", "Stage IIB Fallopian Tube Cancer AJCC v6 and v7", "FIGO Stage IIB Carcinoma of the Fallopian Tube"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Fallopian Tube Cancer AJCC v6 and v7", "shortest_name_length": 31}
{"curie": "UMLS:C3146251", "names": ["Stage IV Colorectal Cancer", "Stage IV Colorectal Cancer AJCC v7", "Stage IV Colorectal (Colon or Rectal) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Colorectal Cancer AJCC v7", "shortest_name_length": 26}
{"curie": "MONDO:0800107", "names": ["anterior deviation infundibular septum", "Anterior deviation of infundibular septum of Fallot type", "Anterior deviation of infundibular septum of Fallot type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anterior deviation infundibular septum", "shortest_name_length": 38}
{"curie": "UMLS:C1336842", "names": ["Type B LyP", "Type B Lymphomatoid Papulosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Type B Lymphomatoid Papulosis", "shortest_name_length": 10}
{"curie": "UMLS:C0343590", "names": ["Tick-Borne Hemorrhagic Fever", "Tick-borne hemorrhagic fever", "tick-borne hemorrhagic fever", "Tick-borne haemorrhagic fever", "tick-borne; hemorrhagic fever", "hemorrhagic fever; tick-borne", "fever; hemorrhagic, tick-borne", "hemorrhagic; fever, tick-borne", "tick-borne hemorrhagic fever (diagnosis)", "Tick-borne hemorrhagic fever (navigational concept)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tick-borne hemorrhagic fever", "shortest_name_length": 28}
{"curie": "UMLS:C3805279", "names": ["Noninfective gingivitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Noninfective gingivitis", "shortest_name_length": 23}
{"curie": "UMLS:C0857323", "names": ["Angioedema of larynx"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Angioedema of larynx", "shortest_name_length": 20}
{"curie": "MONDO:0002968", "names": ["lymphocyst", "lymphocele", "Lymph cyst", "Lymphocyst", "cyst lymph", "Lymphocele", "lymph cyst", "lymphocysts", "lymphocoele", "Lymphocoele", "Lymphoceles", "cysts lymph", "lymphoceles", "Lymphocoeles", "lymphatic cyst", "Lymphatic Cyst", "Lymphatic cyst", "Lymphatic Cysts", "Cyst, Lymphatic", "lymphatic cysts", "Cysts, Lymphatic", "Lymphocele (disorder)", "Lymphocele (diagnosis)", "Cyst of lymphatic tissue", "Cyst of lymphatic tissue (disorder)", "Lymphocyst (morphologic abnormality)", "disorder of lymphatic vessel lymphocele"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphocele", "shortest_name_length": 10}
{"curie": "UMLS:C1333154", "names": ["Typical Alveolar Rhabdomyosarcoma", "Conventional Alveolar Rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conventional Alveolar Rhabdomyosarcoma", "shortest_name_length": 33}
{"curie": "UMLS:C5208246", "names": ["Immune-mediated pancreatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immune-mediated pancreatitis", "shortest_name_length": 28}
{"curie": "UMLS:C4288543", "names": ["Ovarian Luteinized Thecoma Associated with Sclerosing Peritonitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Luteinized Thecoma Associated with Sclerosing Peritonitis", "shortest_name_length": 65}
{"curie": "MONDO:0013045", "names": ["MTBS3", "MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, 3", "mycobacterium tuberculosis, susceptibility to, 3", "Mycobacterium tuberculosis, susceptibility to, type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mycobacterium tuberculosis, susceptibility to, 3", "shortest_name_length": 5}
{"curie": "UMLS:C4683152", "names": ["Stage IIIB Posterior Uveal Melanoma AJCC v8", "Stage IIIB Choroidal and Ciliary Body Melanoma", "Stage IIIB Choroidal and Ciliary Body Melanoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Choroidal and Ciliary Body Melanoma AJCC v8", "shortest_name_length": 43}
{"curie": "MONDO:0007461", "names": ["short stature-valvular heart disease-characteristic facies syndrome", "disproportionate short stature with ptosis and valvular heart lesions", "Disproportionate Short Stature with Ptosis and Valvular Heart Lesions", "DISPROPORTIONATE SHORT STATURE WITH PTOSIS AND VALVULAR HEART LESIONS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short stature-valvular heart disease-characteristic facies syndrome", "shortest_name_length": 67}
{"curie": "MONDO:0014468", "names": ["CMS7", "CMS7A", "congenital myasthenic syndrome 7", "SYT2 congenital myasthenic syndrome", "congenital myasthenic syndrome type 7", "congenital myasthenic syndrome 7 presynaptic", "myasthenic syndrome, congenital, 7, presynaptic", "congenital myasthenic syndrome caused by mutation in SYT2", "myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy", "MYASTHENIC SYNDROME, CONGENITAL, 7A, PRESYNAPTIC, AND DISTAL MOTOR NEUROPATHY, AUTOSOMAL DOMINANT", "myasthenic syndrome, congenital, 7A, presynaptic, and distal motor neuropathy, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myasthenic syndrome 7", "shortest_name_length": 4}
{"curie": "MONDO:0004467", "names": ["Mature Gastric Teratoma", "mature gastric teratoma", "stomach mature teratoma", "Mature teratoma of stomach", "mature teratoma of stomach", "Mature Teratoma of Stomach", "mature teratoma of the stomach", "Mature Teratoma of the Stomach"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mature gastric teratoma", "shortest_name_length": 23}
{"curie": "MONDO:0017567", "names": ["macrodactyly of foot, bilateral", "macrodactyly of toes, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macrodactyly of toes, bilateral", "shortest_name_length": 31}
{"curie": "MONDO:0006831", "names": ["Leukostases", "Leukostasis", "leukostasis", "Leukostasis Syndrome", "Leukostasis syndrome", "Syndrome, Leukostasis", "Leukostasis Syndromes", "Syndromes, Leukostasis", "Leukostasis (morphologic abnormality)", "leukostasis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukostasis", "shortest_name_length": 11}
{"curie": "UMLS:C4049618", "names": ["Mixed tumor, NOS", "Mixed Tumor, NOS", "Mixed Tumor, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mixed Tumor, Not Otherwise Specified", "shortest_name_length": 16}
{"curie": "UMLS:C0160399", "names": ["Open injury of liver", "Injury to Liver with Open Wound into Cavity", "injury of liver with open wound into cavity", "Injury to liver with open wound into cavity", "Injury of liver with open wound into abdominal cavity", "Unspecified injury to liver with open wound into cavity", "injury of liver with open wound into cavity (diagnosis)", "Injury to liver with open wound into cavity, unspecified injury", "Injury of liver with open wound into abdominal cavity (disorder)", "Unspecified injury of liver with open wound into abdominal cavity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of liver with open wound into abdominal cavity", "shortest_name_length": 20}
{"curie": "MONDO:0008047", "names": ["EA1", "EAM", "AEM", "AEMK", "Isaacs", "myokymia 1", "MYOKYMIA 1", "Myokymia 1", "Neuromyotonia", "neuromyotonia", "Isaac Syndrome", "isaac syndrome", "isaacs syndrome", "Isaacs syndrome", "Isaacs Syndrome", "Isaac's syndrome", "Quantal Squander", "isaacs' syndrome", "isaac's syndrome", "Isaacs' Syndrome", "quantal squander", "Continuous Myokymia", "Continuous Myokymias", "Myokymia, Continuous", "Myokymias, Continuous", "Episodic ataxia type 1", "episodic ataxia type 1", "Episodic Ataxia, Type 1", "Isaacs-Mertens Syndrome", "episodic ataxia, type 1", "EPISODIC ATAXIA, TYPE 1", "Isaacs Mertens Syndrome", "Isaacs-Mertens syndrome", "ISAACS-MERTENS SYNDROME", "Neuromyotonia (disorder)", "Quantal squander syndrome", "Gamstorp-Wohlfart syndrome", "Gamstorp Wohlfart Syndrome", "Isaacs syndrome (disorder)", "Gamstorp-Wohlfart Syndrome", "Isaacs syndrome (diagnosis)", "Episodic ataxia type 1 (EA1)", "EPISODIC ATAXIA WITH MYOKYMIA", "Episodic ataxia with myokymia", "episodic ataxia with myokymia", "MYOKYMIA WITH PERIODIC ATAXIA", "Myokymia with Periodic Ataxia", "myokymia with periodic ataxia", "Episodic Ataxia with Myokymia", "Isaacs Pseudomyotonia Syndrome", "ATAXIA, EPISODIC, WITH MYOKYMIA", "ataxia, episodic, with myokymia", "Ataxia, Episodic, with Myokymia", "KCNA1 hereditary episodic ataxia", "continuous muscle fiber activity", "Continuous muscle fiber activity", "Continuous muscle fibre activity", "Episodic ataxia type 1 (disorder)", "Pseudomyotonia Syndrome of Isaacs", "episodic ataxia/myokymia syndrome", "Peripheral nerve hyperexcitability", "Continuous Muscle Activity Syndrome", "Syndrome of Continuous Muscle Activity", "acetazolamide-responsive periodic ataxia", "myokymia 1 with or without hypomagnesemia", "Myokymia 1 With Or Without Hypomagnesemia", "Continuous muscle fiber activity syndrome", "MYOKYMIA 1 WITH OR WITHOUT HYPOMAGNESEMIA", "continuous muscle fiber activity, hereditary", "hereditary paroxysmal ataxia with neuromyotonia", "paroxysmal ataxia with neuromyotonia, hereditary", "Paroxysmal Ataxia with Neuromyotonia, Hereditary", "PAROXYSMAL ATAXIA WITH NEUROMYOTONIA, HEREDITARY", "Myokymia, Myotonia, Muscle Wasting, And Hyperhidrosis", "hereditary episodic ataxia caused by mutation in KCNA1", "familial paroxysmal kinesigenic ataxia and continuous myokymia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "episodic ataxia type 1", "shortest_name_length": 3}
{"curie": "MONDO:0005585", "names": ["chemotherapy-induced hypertension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chemotherapy-induced hypertension", "shortest_name_length": 33}
{"curie": "MONDO:0016157", "names": ["qualitative or quantitative defects of fukutin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of fukutin", "shortest_name_length": 46}
{"curie": "UMLS:C1332624", "names": ["Metastatic Breast Cancer in the Brain", "Breast Carcinoma Metastatic to the Brain", "Breast Carcinoma Metastatic in the Brain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Carcinoma Metastatic in the Brain", "shortest_name_length": 37}
{"curie": "MONDO:0012914", "names": ["Del(1)(q21)", "1q21.1 Deletion", "Monosomy 1q21.1", "monosomy 1q21.1", "1q21.1 Microdeletion", "1q21.1 microdeletion", "1q21.1 microdeletion syndrome", "1q21.1 contiguous gene deletion", "1q21.1 Contiguous Gene Deletion", "Microdeletion of chromosome 1q21.1", "Chromosome 1q21.1 Deletion Syndrome", "chromosome 1q21.1 deletion syndrome", "Chromosome 1q21.1 deletion syndrome", "chromosome 1q21.1 microdeletion syndrome", "1q21.1 microdeletion syndrome (disorder)", "chromosome 1q21.1 deletion syndrome, 1.35-MB", "CHROMOSOME 1q21.1 DELETION SYNDROME, 1.35-MB", "Chromosome 1q21.1 Deletion Syndrome, 1.35-Mb", "chromosome 1q21.1 deletion syndrome, isolated cases", "1q21.1 recurrent microdeletion (susceptibility locus for neurodevelopmental disorders)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 1q21.1 deletion syndrome", "shortest_name_length": 11}
{"curie": "UMLS:C0948369", "names": ["Myocardial reinfarction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myocardial reinfarction", "shortest_name_length": 23}
{"curie": "MONDO:0003750", "names": ["childhood germ cell CNS tumor", "Childhood CNS Germ Cell Tumor", "childhood CNS germ cell tumor", "pediatric CNS germ cell tumor", "Pediatric CNS Germ Cell Tumor", "CNS tumor, childhood germ cell", "childhood CNS tumor, germ cell", "germ cell CNS tumor, childhood", "CNS tumor, pediatric germ cell", "pediatric germ cell tumor of CNS", "Childhood CNS Germ Cell Neoplasm", "childhood germ cell tumor of CNS", "Pediatric CNS Germ Cell Neoplasm", "Childhood Germ Cell Tumor of CNS", "childhood CNS germ cell neoplasm", "Pediatric Germ Cell Tumor of CNS", "pediatric CNS germ cell neoplasm", "Pediatric Germ Cell Neoplasm of CNS", "Childhood Germ Cell Neoplasm of CNS", "pediatric germ cell neoplasm of CNS", "childhood germ cell neoplasm of CNS", "Pediatric Germ Cell Tumor of the CNS", "paediatric germ cell neoplasm of CNS", "Childhood Germ Cell Tumor of the CNS", "pediatric germ cell tumor of the CNS", "childhood germ cell tumor of the CNS", "central nervous system germ cell tumor", "Central Nervous System Germ Cell Tumor", "Pediatric Germ Cell Neoplasm of the CNS", "pediatric germ cell neoplasm of the CNS", "Childhood Germ Cell Neoplasm of the CNS", "childhood germ cell neoplasm of the CNS", "Pediatric Central Nervous System Germ Cell Tumor", "pediatric central nervous system germ cell tumor", "Childhood Central Nervous System Germ Cell Tumor", "central nervous system childhood germ cell tumor", "childhood central nervous system germ cell tumor", "central nervous system childhood germ cell tumour", "central nervous system pediatric germ cell cancer", "central nervous system tumor, germ cell, childhood", "childhood germ cell tumor of central nervous system", "pediatric central nervous system germ cell neoplasm", "Pediatric Central Nervous System Germ Cell Neoplasm", "childhood central nervous system germ cell neoplasm", "pediatric germ cell tumor of central nervous system", "Pediatric Germ Cell Tumor of Central Nervous System", "Childhood Central Nervous System Germ Cell Neoplasm", "Childhood Germ Cell Tumor of Central Nervous System", "Pediatric Germ Cell Neoplasm of Central Nervous System", "Childhood Germ Cell Neoplasm of Central Nervous System", "pediatric germ cell neoplasm of central nervous system", "childhood germ cell neoplasm of central nervous system", "Pediatric Germ Cell Tumor of the Central Nervous System", "Childhood Germ Cell Tumor of the Central Nervous System", "childhood germ cell tumor of the central nervous system", "pediatric germ cell tumor of the central nervous system", "pediatric germ cell neoplasm of the central nervous system", "Pediatric Germ Cell Neoplasm of the Central Nervous System", "Childhood Germ Cell Neoplasm of the Central Nervous System", "childhood germ cell neoplasm of the central nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood central nervous system germ cell tumor", "shortest_name_length": 29}
{"curie": "MONDO:0010762", "names": ["Hodgkin Disease, Y-Linked Pseudoautosomal", "Hodgkin disease, Y-linked Pseudoautosomal", "HODGKIN DISEASE, Y-LINKED PSEUDOAUTOSOMAL", "lymphoma, Hodgkin, Y-linked pseudoautosomal", "LYMPHOMA, HODGKIN, Y-LINKED PSEUDOAUTOSOMAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphoma, Hodgkin, Y-linked pseudoautosomal", "shortest_name_length": 41}
{"curie": "MONDO:0032574", "names": ["OCBMD", "OSTEOCHONDRODYSPLASIA, BRACHYDACTYLY, AND OVERLAPPING MALFORMED DIGITS", "osteochondrodysplasia, brachydactyly, and overlapping malformed digits"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteochondrodysplasia, brachydactyly, and overlapping malformed digits", "shortest_name_length": 5}
{"curie": "UMLS:C0032965", "names": ["INFECTION PREGNANCY", "pregnancy infection", "pregnancy; infection", "c.pregnancy; infection", "Pregnancy, Infections in", "Infections and Pregnancy", "Other infectious conditions", "infection complicat pregnancy", "Infection complicat pregnancy", "c.pregnancy; infectious disease", "c.pregnancy; disease, infective", "Infectious Pregnancy Complication", "infection; complicating pregnancy", "Infectious Pregnancy Complications", "Pregnancy Complication, Infectious", "Pregnancy Complications, Infectious", "Pregnancy, Infectious Complications", "Complications, Infectious Pregnancy", "pregnancy complications caused by infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pregnancy Complications, Infectious", "shortest_name_length": 19}
{"curie": "UMLS:C0036902", "names": ["Sexual arousal disorder", "sexual arousal disorder", "Sexual Arousal Disorder", "Sexual arousal disorders", "Sexual Arousal Disorders", "sexual arousal disorders", "Disorders, Sexual Arousal", "Arousal Disorders, Sexual", "Sexual arousal disorder, NOS", "Sexual arousal disorder (disorder)", "sexual arousal disorders (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sexual Arousal Disorder", "shortest_name_length": 23}
{"curie": "MONDO:0019513", "names": ["esophageal malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophageal malformation", "shortest_name_length": 23}
{"curie": "UMLS:C0279744", "names": ["Grade III Salivary Gland Mucoepidermoid Carcinoma", "high-grade salivary gland mucoepidermoid carcinoma", "High Grade Salivary Gland Mucoepidermoid Carcinoma", "salivary gland mucoepidermoid carcinoma high grade", "high grade mucoepidermoid carcinoma, salivary gland", "mucoepidermoid carcinoma high grade, salivary gland", "Grade III Mucoepidermoid Carcinoma of Salivary Gland", "High-Grade Mucoepidermoid Carcinoma of Salivary Gland", "Grade III Mucoepidermoid Carcinoma of the Salivary Gland", "High-Grade Mucoepidermoid Carcinoma of the Salivary Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Salivary Gland Mucoepidermoid Carcinoma", "shortest_name_length": 49}
{"curie": "MONDO:0100186", "names": ["HPABH4B", "GTPCH deficiency", "GTPCH Deficiency", "GTP Cyclohydrolase I Deficiency", "GTP cyclohydrolase I deficiency", "GTP CYCLOHYDROLASE I DEFICIENCY", "GTP cyclohydrolase 1 deficiency", "BH4-deficient hyperphenylalaninemia B", "Hyperphenylalaninemia, BH4-Deficient, B", "hyperphenylalaninemia, BH4-deficient, B", "HYPERPHENYLALANINEMIA, BH4-DEFICIENT, B", "hyperphenylalaninemia, Bh4-deficient, type B", "Hyperphenylalaninemia with neopterin deficiency", "Hyperphenylalaninaemia with neopterin deficiency", "Guanosine triphosphate cyclohydrolase I deficiency", "Guanosine-5-triphosphate cyclohydrolase deficiency", "tetrahydrobiopterin-deficient hyperphenylalaninemia B", "GTP - Guanosine-5-triphosphate cyclohydrolase deficiency", "Guanosine triphosphate (GTP) cyclohydrolase I deficiency", "Hyperphenylalaninemia due to GTP cyclohydrolase deficiency", "hyperphenylalaninemia due to GTP cyclohydrolase deficiency", "GTP cyclohydrolase I deficiency with hyperphenylalaninemia", "Guanosine triphosphate cyclohydrolase I deficiency (disorder)", "HYPERPHENYLALANINEMIA, TETRAHYDROBIOPTERIN-DEFICIENT, DUE TO GTP CYCLOHYDROLASE I DEFICIENCY", "hyperphenylalaninemia, tetrahydrobiopterin-deficient, due to GTP cyclohydrolase 1 deficiency", "Hyperphenylalaninemia, Tetrahydrobiopterin-Deficient, Due To GTP Cyclohydrolase I Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "GTP cyclohydrolase I deficiency with hyperphenylalaninemia", "shortest_name_length": 7}
{"curie": "UMLS:C3272308", "names": ["Cardiac Valve Injury", "Cardiac valve injury", "Injury of cardiac valve", "Trauma to cardiac valve", "Injury of cardiac valve (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of cardiac valve", "shortest_name_length": 20}
{"curie": "UMLS:C0242966", "names": ["SIRS", "Sepsis syndrome", "sepsis syndrome", "Sepsis Syndrome", "septic syndrome", "SEPSIS SYNDROME", "Septic syndrome", "syndrome sepsis", "Syndrome, Sepsis", "Sepsis Syndromes", "Syndromes, Sepsis", "Abacteraemic sepsis", "Culture-negative sepsis", "Sepsis syndrome (disorder)", "Sepsis syndrome (diagnosis)", "organ dysfunction syndrome sepsis", "Systemic Inflammatory Response Syndrome", "SYSTEMIC INFLAMMATORY RESPONSE SYNDROME", "Systemic inflammatory response syndrome", "systemic inflammatory response syndrome", "Inflammatory Response Syndrome, Systemic", "SIRS - System inflammatory response syndrome", "Systemic inflammatory response syndrome (SIRS)", "systemic inflammatory response syndrome (SIRS)", "Systemic inflammatory response syndrome (disorder)", "Systemic inflammatory response syndrome (SIRS) NOS", "Systemic inflammatory response syndrome, unspecified", "systemic inflammatory response syndrome (SIRS) (diagnosis)", "systemic inflammatory response syndrome (SIRS) due to infectious process", "systemic inflammatory response syndrome (SIRS) due to infectious process (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Systemic Inflammatory Response Syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0751075", "names": ["cancer digestive system", "Digestive System Cancer", "digestive system cancer", "digestive system cancers", "Digestive System Cancers", "Cancer, Digestive System", "Neoplasm malig;digestive", "cancers digestive system", "Cancers, Digestive System", "Cancer of digestive system", "Cancer of Digestive System", "Cancer of the Digestive System", "cancer of the digestive system", "Malignant neoplasm of digestive system", "malignant neosplasm of the digestive system", "Malignant neoplasm of digestive system (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cancer of Digestive System", "shortest_name_length": 23}
{"curie": "UMLS:C0333641", "names": ["atrophy", "Atrophy", "atrophic", "Atrophic", "ATROPHIES", "atrophies", "Atrophies", "atrophied", "atrophying", "Atrophy NOS", "Atrophy, NOS", "Atrophy (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atrophic", "shortest_name_length": 7}
{"curie": "MONDO:0001148", "names": ["iliac vein thrombophlebitis", "thrombophlebitis of iliac vein", "Thrombophlebitis of iliac vein", "Thrombophlebitis of iliac vein (disorder)", "thrombophlebitis of iliac vein (diagnosis)", "Phlebitis and thrombophlebitis of iliac vein", "Phlebitis and thrombophlebitis of the iliac vein", "phlebitis and thrombophlebitis of the iliac vein"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "iliac vein thrombophlebitis", "shortest_name_length": 27}
{"curie": "MONDO:0018816", "names": ["NSC", "sclerosing cholangitis, neonatal", "SCLEROSING CHOLANGITIS, NEONATAL", "isolated neonatal sclerosing cholangitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated neonatal sclerosing cholangitis", "shortest_name_length": 3}
{"curie": "UMLS:C0280401", "names": ["Relapsed Larynx Epidermoid Carcinoma", "Recurrent Larynx Epidermoid Carcinoma", "Relapsed Larynx Squamous Cell Carcinoma", "Relapsed Epidermoid Carcinoma of Larynx", "Relapsed Laryngeal Epidermoid Carcinoma", "Recurrent Laryngeal Epidermoid Carcinoma", "Recurrent Epidermoid Carcinoma of Larynx", "Recurrent Larynx Squamous Cell Carcinoma", "larynx squamous cell carcinoma, recurrent", "Relapsed Squamous Cell Carcinoma of Larynx", "Relapsed Laryngeal Squamous Cell Carcinoma", "Laryngeal squamous cell carcinoma recurrent", "Recurrent Squamous Cell Carcinoma of Larynx", "Relapsed Epidermoid Carcinoma of the Larynx", "Recurrent Laryngeal Squamous Cell Carcinoma", "Recurrent Epidermoid Carcinoma of the Larynx", "laryngeal squamous cell carcinoma, recurrent", "epidermoid carcinoma of the larynx, recurrent", "Relapsed Squamous Cell Carcinoma of the Larynx", "Recurrent Squamous Cell Carcinoma of the Larynx", "recurrent squamous cell carcinoma of the larynx", "squamous cell carcinoma of the larynx, recurrent", "Recurrent Laryngeal Throat Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laryngeal squamous cell carcinoma recurrent", "shortest_name_length": 36}
{"curie": "MONDO:0007995", "names": ["CATM", "MCOPCT1", "microphthalmia with cataract 1", "congenital cataract with microphthalmia", "Cataract, Congenital with Microphthalmia", "microphthalmia, isolated, with cataract 1", "Microphthalmia, Isolated, with Cataract 1", "cataract, congenital, with microphthalmia", "CATARACT, CONGENITAL, WITH MICROPHTHALMIA", "MICROPHTHALMIA, ISOLATED, WITH CATARACT 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microphthalmia, isolated, with cataract 1", "shortest_name_length": 4}
{"curie": "MONDO:0015040", "names": ["RAEB I", "RAEB 1", "RAEB-I", "RAEB-1", "MDS-EB-1", "refractory anemia with excess blasts-1", "Refractory anemia with excess blasts-1", "Refractory anemia with excess blasts I", "Refractory anaemia with excess blasts I", "Refractory anaemia with excess blasts-1", "Refractory anemia with excess of blasts 1", "refractory anemia with excess blasts type 1", "Refractory anemia with excess blasts type 1", "Myelodysplastic syndrome with excess blasts-1", "myelodysplastic syndrome with excess blasts-1", "myelodysplastic syndrome with Excess blasts-1", "Myelodysplastic Syndrome with Excess Blasts-1", "refractory anemia with excess blasts-1 (diagnosis)", "Myelodysplastic syndrome with excess blasts-1 (disorder)", "MDS-EB-1 - myelodysplastic syndrome with excess blasts-1", "Myelodysplastic syndrome with excess blasts-1 (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myelodysplastic syndrome with excess blasts-1", "shortest_name_length": 6}
{"curie": "MONDO:0008086", "names": ["HSN1A", "HSN IA", "HSN 1A", "HSAN1A", "HSAN IA", "HSAN 1A", "neuropathy, hereditary sensory, type 1A", "NEUROPATHY, HEREDITARY SENSORY, TYPE IA", "Hereditary sensory autonomic neuropathy type IA", "hereditary sensory and autonomic neuropathy type 1A", "hereditary sensory and autonomic neuropathy type IA", "NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA", "neuropathy, hereditary sensory and autonomic, type 1A", "neuropathy, hereditary sensory and autonomic, type IA", "SPTLC1 hereditary sensory and autonomic neuropathy type 1", "Hereditary sensory autonomic neuropathy type IA (disorder)", "neuropathy, hereditary sensory radicular, autosomal dominant, type 1A", "NEUROPATHY, HEREDITARY SENSORY RADICULAR, AUTOSOMAL DOMINANT, TYPE 1A", "hereditary sensory and autonomic neuropathy type 1 caused by mutation in SPTLC1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuropathy, hereditary sensory and autonomic, type 1A", "shortest_name_length": 5}
{"curie": "UMLS:C0858346", "names": ["Gastrointestinal ulcer perforation", "Gastrointestinal ulcer perforated NOS", "Gastrointestinal ulcer perforation NOS", "Gastrointestinal ulceration and perforation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal ulcer perforation", "shortest_name_length": 34}
{"curie": "MONDO:0006161", "names": ["Colorectal Juvenile Polyp", "colorectal juvenile polyp", "Colorectal Retention Polyp", "Large Bowel Juvenile Polyp", "large bowel juvenile polyp", "colorectal retention polyp", "Juvenile Polyp of Large Bowel", "juvenile polyp of large bowel", "Juvenile polyps of large bowel", "Large Intestinal Juvenile Polyp", "Retention polyps of large bowel", "large intestinal juvenile polyp", "Juvenile Polyp of the Large Bowel", "juvenile polyp of the large bowel"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorectal juvenile polyp", "shortest_name_length": 25}
{"curie": "UMLS:C5420078", "names": ["Sinonasal Extranodal NK/T-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Extranodal NK/T-Cell Lymphoma", "shortest_name_length": 39}
{"curie": "MONDO:0003473", "names": ["Spinal Ependymoma", "Spinal ependymoma", "Spinal Cord Ependymoma", "spinal cord ependymoma", "SPINAL CORD, EPENDYMOMA", "Ependymoma of spinal cord", "Ependymoma of Spinal Cord", "ependymoma of spinal cord", "Ependymoma of the Spinal Cord", "ependymoma of the spinal cord", "Ependymal tumor of spinal cord", "Ependymal tumour of spinal cord", "Ependymoma of spinal cord (disorder)", "Ependymal neoplasm of the Spinal Cord", "ependymal neoplasm of the spinal cord", "ependymoma of spinal cord (diagnosis)", "Spinal Cord Ependymoma without MYCN Amplification"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal cord ependymoma", "shortest_name_length": 17}
{"curie": "UMLS:C5418797", "names": ["Advanced Vaginal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Vaginal Carcinoma", "shortest_name_length": 26}
{"curie": "UMLS:C4553878", "names": ["Stage IVA Thyroid Gland Follicular Cancer", "Stage IVA Thyroid Gland Follicular Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Thyroid Gland Follicular Carcinoma AJCC v8", "shortest_name_length": 41}
{"curie": "UMLS:C3898098", "names": ["Ophthalmorrhexis", "Open globe injury", "Open Globe Injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Open globe injury", "shortest_name_length": 16}
{"curie": "MONDO:0043343", "names": ["Chilaiditi anomaly", "Chilaiditis anomaly", "Chilaiditi syndrome", "anomaly, Chilaiditi", "Chilaiditi Syndrome", "Chilaiditis syndrome", "Syndrome, Chilaiditi", "Chilaiditis Syndrome", "syndrome, Chilaiditi", "Chilaiditi's anomaly", "Chilaiditi's Syndrome", "anomaly, Chilaiditi's", "chilaiditi's syndrome", "Chilaiditi's syndrome", "Syndrome, Chilaiditi's", "syndrome, Chilaiditi's", "subphrenic interposition syndrome", "Subphrenic interposition syndrome", "Hepatodiaphragmatic colonic interposition", "hepatodiaphragmatic colonic interposition", "Subphrenic interposition syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chilaiditi syndrome", "shortest_name_length": 18}
{"curie": "MONDO:0004882", "names": ["choroidal angioid streaks", "angioid streaks of choroid", "Angioid streaks of choroid", "optic choroid angioid streaks", "angioid streaks were observed", "angioid streaks of optic choroid", "Angioid streaks of choroid (disorder)", "choroidal angioid streaks (diagnosis)", "angioid streaks of choroid (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angioid streaks of choroid", "shortest_name_length": 25}
{"curie": "UMLS:C1370832", "names": ["recurrent childhood hepatoma", "Recurrent Pediatric Hepatoma", "recurrent pediatric hepatoma", "Recurrent Childhood Hepatoma", "pediatric hepatoma, recurrent", "childhood hepatoma, recurrent", "hepatoma, childhood, recurrent", "hepatoma, pediatric, recurrent", "Recurrent Hepatocellular Cancer", "Recurrent Pediatric Hepatocellular Carcinoma", "Recurrent Childhood Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Hepatocellular Carcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0007174", "names": ["lgl", "LGL syndrome", "lown-ganong-lavine", "Lown-Ganong-Levine", "Lown-Ganong-Levine syndrome", "Lown-Ganong-Levine Syndrome", "Lown Ganong Levine syndrome", "lown ganong levine syndrome", "lown-ganong-levine syndrome", "Lown Ganong Levine Syndrome", "Syndrome, Lown-Ganong-Levine", "lown ganong levine syndrome (LGL)", "Short PR Normal QRS Complex Syndrome", "Short PR-Normal QRS Complex Syndrome", "Lown-Ganong-Levine syndrome (disorder)", "Lown-Ganong-Levine syndrome (diagnosis)", "Atrial tachyarrhythmia with short PR interval", "Atrial Tachyarrhythmia with Short PR Interval", "ATRIAL TACHYARRHYTHMIA WITH SHORT PR INTERVAL", "atrial tachyarrhythmia with short PR interval", "Syndrome of short P-R interval, normal QRS complexes AND supraventricular tachycardias", "Syndrome of short P-R interval, normal QRS complexes and supraventricular tachycardias", "Syndrome of short P-R interval, normal QRS complexes, and supraventricular tachycardias", "syndrome of short P-R interval, normal QRS complexes, and supraventricular tachycardias"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lown-Ganong-Levine syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0015493", "names": ["lipoatrophy with diabetes, leukomelanodermic papules, liver steatosis, and hypertrophic cardiomyopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lipoatrophy with diabetes, leukomelanodermic papules, liver steatosis, and hypertrophic cardiomyopathy", "shortest_name_length": 102}
{"curie": "MONDO:0008564", "names": ["VCF", "DGS", "DGS1", "DGCR", "FACES", "22q11DS", "Catch22", "CATCH22", "CATCH 22", "CATCH-22", "DiGeorge", "Sphrintzen", "monosomy 22q", "22q- syndrome", "Takao syndrome", "Monosomy 22q11", "22q11 deletion", "digeorge anomaly", "DiGeorge anomaly", "DiGeorge Anomaly", "digeorge sequence", "DiGeorge Syndrome", "DiGeorge syndrome", "DiGeorge Sequence", "digeorge syndrome", "DIGEORGE SYNDROME", "DiGeorge sequence", "del(22q) syndrome", "thymic hypoplasia", "digeorges syndrome", "di george syndrome", "Di George syndrome", "DI GEORGE SYNDROME", "syndrome di george", "Takao VCF Syndrome", "Di-George syndrome", "digeorge syndromes", "Takao VCF syndrome", "Syndrome, DiGeorge", "TAKAO VCF SYNDROME", "Shprintzen syndrome", "Shprintzen Syndrome", "DiGeorge's syndrome", "Digeorge's syndrome", "digeorge's syndrome", "Sedlackova syndrome", "di georges syndrome", "DiGeorge's Syndrome", "di george's syndrome", "partial monosomy 22q", "Di George's syndrome", "22q deletion syndrome", "deletion 22q syndrome", "Microdeletion 22q11.2", "Branchial arch syndrome", "DiGeorge syndrome (DGS)", "branchial arch syndrome", "chromosome 22q monosomy", "Thymic Aplasia Syndrome", "thymic aplasia syndrome", "22q deletion syndrome(s)", "DiGeorge syndrome type 1", "22q Deletion Syndrome(s)", "DiGeorge Syndrome Type 1", "velocardiofacial syndrome", "Pharyngeal Pouch Syndrome", "Pharyngeal pouch syndrome", "22q11.2 Deletion syndrome", "Velocardiofacial syndrome", "22q11.2 Deletion Syndrome", "pharyngeal pouch syndrome", "22q11.2 deletion syndrome", "Thymic hypoplasia syndrome", "pharyngeal pouch; syndrome", "syndrome; pharyngeal pouch", "Thymic-parathyroid aplasia", "aplasia; parathyroid-thymic", "velo-cardio-facial syndrome", "parathyroid-thymic; aplasia", "Cayler cardiofacial syndrome", "DiGeorge sequence (diagnosis)", "chromosome 22q deletion syndrome", "Conotruncal anomaly face syndrome", "Congenital thymic aplasia syndrome", "DIGEORGE SYNDROME CHROMOSOME REGION", "DiGeorge syndrome chromosome region", "chromosome 22Q11.2 deletion syndrome", "22q11.2 deletion syndrome (disorder)", "CHROMOSOME 22q11.2 DELETION SYNDROME", "hypoplasia of thymus and parathyroids", "Hypoplasia of Thymus and Parathyroids", "HYPOPLASIA OF THYMUS AND PARATHYROIDS", "Autosomal Dominant Opitz G-Bbb Syndrome", "Autosomal Dominant Opitz G Bbb Syndrome", "thymic and parathyroid agenesis syndrome", "Third and fourth pharyngeal arch syndrome", "Third and fourth pharyngeal pouch syndrome", "Third and Fourth Pharyngeal Pouch Syndrome", "THIRD AND FOURTH PHARYNGEAL POUCH SYNDROME", "third and fourth pharyngeal pouch syndrome", "Agenesis of the parathyroid and thymus glands", "Familial Third and Fourth Pharyngeal Pouch Syndrome", "familial third and fourth pharyngeal pouch syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DiGeorge syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0016682", "names": ["Monstrocellular sarcoma", "Giant Cell Glioblastoma", "giant cell glioblastoma", "Giant cell glioblastoma", "Giant Cell Glioblastomas", "Glioblastoma, Giant Cell", "Glioblastomas, Giant Cell", "Monstrocellular sarcoma [obs]", "giant cell; glioblastoma, unspecified site", "glioblastoma; giant cell, unspecified site", "Giant cell glioblastoma (morphologic abnormality)", "Monstrocellular sarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "giant cell glioblastoma", "shortest_name_length": 23}
{"curie": "MONDO:0019150", "names": ["familial isolated restrictive cardiomyopathy", "familial or idiopathic restrictive cardiomyopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial isolated restrictive cardiomyopathy", "shortest_name_length": 44}
{"curie": "MONDO:0030376", "names": ["MARTS2", "Martsolf syndrome 2", "MARTSOLF SYNDROME 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Martsolf syndrome 2", "shortest_name_length": 6}
{"curie": "UMLS:C4528645", "names": ["AIDS-Related Anal Canal Cancer", "AIDS-Related Anal Canal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Anal Canal Carcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0018542", "names": ["SCN", "SCN3", "Kostmann", "KOSTMANN DISEASE", "Kostmann disease", "Kostmann Syndrome", "Kostmann syndrome", "Kostmann's disease", "Kostmann's Syndrome", "Primary neutropenia", "kostmann's syndrome", "Kostmann's syndrome", "Kostmann neutropenia", "Congenital Neutropenia", "Congenital neutropenia", "congenital neutropenia", "Infantile agranulocytosis", "AGRANULOCYTOSIS, INFANTILE", "Agranulocytosis, Infantile", "congenital agranulocytosis", "Congenital Agranulocytosis", "Congenital agranulocytosis", "Kostmann's Agranulocytosis", "Kostmann syndrome (disorder)", "Severe Congenital Neutropenia", "Severe congenital neutropenia", "severe congenital neutropenia", "Neutropenia, severe congenital", "neutropenia, severe congenital", "Autosomal Recessive SCN, Type 3", "Congenital neutropenia (disorder)", "Infantile genetic agranulocytosis", "agranulocytosis genetic infantile", "infantile genetic agranulocytosis", "agranulocytosis infantile genetic", "Agranulocytosis, infantile genetic", "congenital neutropenia (diagnosis)", "Severe congenital neutropenia type 3", "Severe infantile genetic neutropenia", "Severe Infantile Genetic Neutropenia", "Severe congenital neutropaenia type 3", "Severe infantile genetic agranulocytosis", "infantile genetic agranulocytosis (diagnosis)", "Neutropenia, Severe Congenital, Autosomal Recessive 3", "Autosomal dominant or sporadic congenital neutropenia", "Neutropenia, Severe Congenital, 3, Autosomal Recessive", "NEUTROPENIA, SEVERE CONGENITAL, 3, AUTOSOMAL RECESSIVE", "Severe Congenital Neutropenia Type 3, Autosomal Recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe congenital neutropenia", "shortest_name_length": 3}
{"curie": "OMIM:615221", "names": ["BMND16", "OSTEOPOROSIS, EARLY-ONSET, SUSCEPTIBILITY TO", "BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 16"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 6}
{"curie": "MONDO:0042976", "names": ["Vitamin B deficiency", "vitamin B deficiency", "vitamin b deficiency", "VITAMIN DEFICIENCY B", "Vitamin B Deficiency", "Deficiency, Vitamin B", "deficiency, vitamin B", "b deficiency vitamins", "vitamin B deficiencies", "Vitamin B Deficiencies", "vitamin b deficiencies", "Deficiencies, Vitamin B", "Deficiency of vitamin B", "deficiencies, vitamin B", "deficiency of vitamin b", "Vitamin B deficiency, NOS", "vitamin B-complex deficiency", "Vitamin B-complex deficiency", "vitamin b complex deficiency", "Vitamin B complex deficiency", "vitamin; deficiency, group B", "deficiency; vitamin, group B", "b complex deficiencies vitamin", "Vitamin B deficiency (disorder)", "vitamin B deficiency (diagnosis)", "deficiency; vitamin, B (complex)", "Unspecified vitamin B deficiency", "Vitamin B complex deficiency NOS", "vitamin; deficiency, B (complex)", "Vitamin B deficiency, unspecified", "Vitamin B-complex deficiency, NOS", "Deficiency of B-complex components", "Vitamin B complex deficiency disease", "Vitamin B-complex deficiency (disorder)", "vitamin B-complex deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitamin B deficiency", "shortest_name_length": 20}
{"curie": "MONDO:0010293", "names": ["HEDID", "Eda-Id", "Xhm-Ed", "HED-ID", "EDA-ID", "Ectodermal Dysplasia and Immunodeficiency", "ectodermal dysplasia and immune deficiency", "anhidrotic ectodermal dysplasia with immunodeficiency", "Anhidrotic ectodermal dysplasia with immunodeficiency", "Anhidrotic ectodermal dysplasia with immune deficiency", "anhidrotic ectodermal dysplasia with immune deficiency", "Anhidrotic Ectodermal Dysplasia with Immune Deficiency", "Hypohidrotic ectodermal dysplasia with immunodeficiency", "hypohidrotic ectodermal dysplasia with immunodeficiency", "Hypohidrotic ectodermal dysplasia with immune deficiency", "ectodermal dysplasia, anhidrotic, with immune deficiency", "hypohidrotic ectodermal dysplasia with immune deficiency", "Ectodermal Dysplasia, Anhidrotic, with Immune Deficiency", "Hypohidrotic Ectodermal Dysplasia with Immune Deficiency", "ectodermal dysplasia, hypohidrotic, with immune deficiency", "ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH IMMUNE DEFICIENCY", "Ectodermal dysplasia, hypohidrotic, with immune deficiency", "Hyper-IgM immunodeficiency with hypohidrotic ectodermal dysplasia", "Anhidrotic ectodermal dysplasia with immune deficiency (disorder)", "hyper-IgM immunodeficiency, X-linked, with hypohidrotic ectodermal dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia and immune deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0000621", "names": ["immune system cancer", "cancer of immune system", "malignant immune system neoplasm", "malignant neoplasm of immune system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immune system cancer", "shortest_name_length": 20}
{"curie": "MONDO:0005848", "names": ["Miliary TB", "miliary tb", "disseminated tb", "Disseminated TB", "Miliary Tuberculoses", "miliary tuberculosis", "TUBERCULOSIS MILIARY", "Miliary Tuberculosis", "miliary; tuberculous", "Miliary tuberculosis", "Tuberculoses, Miliary", "TUBERCULOSIS, MILIARY", "Tuberculosis, Miliary", "tuberculosis; miliary", "generalized tuberculosis", "generalised tuberculosis", "Generalized tuberculosis", "Tuberculosis;generalised", "Generalised tuberculosis", "Tuberculosis generalized", "disseminated tuberculosis", "disseminated; tuberculous", "TUBERCULOSIS DISSEMINATED", "Disseminated tuberculosis", "Miliary tuberculosis, NOS", "disseminating tuberculosis", "MTB - Miliary tuberculosis", "acute miliary tuberculosis", "Acute miliary tuberculosis", "tuberculosis; disseminated", "Miliary tuberculosis, acute", "tuberculosis; miliary, acute", "Miliary tuberculosis (disorder)", "miliary tuberculosis (diagnosis)", "Unspecified miliary tuberculosis", "Miliary tuberculosis, unspecified", "Tuberculosis miliaris disseminata", "tuberculosis miliaris disseminata", "Disseminated tuberculosis (disorder)", "disseminated tuberculosis (diagnosis)", "Acute miliary tuberculosis (disorder)", "acute miliary tuberculosis (diagnosis)", "Mycobacterium tuberculosis disseminated", "Acute miliary tuberculosis, unspecified", "Tuberculosis generalized (excluding R70)", "Miliary tuberculosis, unspecified, unspecified", "Acute miliary tuberculosis, unspecified examination", "Unspecified miliary tuberculosis, unspecified examination"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "miliary tuberculosis", "shortest_name_length": 10}
{"curie": "MONDO:0013151", "names": ["CACD3", "Choroidal Dystrophy, Central Areolar 3", "CHOROIDAL DYSTROPHY, CENTRAL AREOLAR, 3", "choroidal dystrophy, central areolar, 3", "Choroidal Dystrophy, Central Areolar, With Or Without Drusen", "CHOROIDAL DYSTROPHY, CENTRAL AREOLAR, WITH OR WITHOUT DRUSEN", "choroidal dystrophy, central areolar, with or without drusen"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choroidal dystrophy, central areolar, 3", "shortest_name_length": 5}
{"curie": "MONDO:0002488", "names": ["Intraductal Breast Neoplasm", "intraductal breast neoplasm", "Breast Intraductal Neoplasm", "Intraductal breast neoplasm", "Breast Intraductal  Neoplasm", "intraductal breast benign neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intraductal breast neoplasm", "shortest_name_length": 27}
{"curie": "UMLS:C5238955", "names": ["IDH-DS", "IDH Inhibitor Associated Differentiation Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IDH Inhibitor Associated Differentiation Syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C4553696", "names": ["Stage IIIC Uterine Corpus Cancer AJCC v8", "Stage IIIC Uterine (including Endometrial) Cancer", "Stage IIIC Uterine Corpus Carcinoma or Carcinosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Uterine Corpus Cancer AJCC v8", "shortest_name_length": 40}
{"curie": "UMLS:C1266124", "names": ["Congenital Fibrosarcoma", "Neonatal Pulmonary Hamartoma", "Myofibroblastic tumor, peribronchial", "Myofibroblastic tumour, peribronchial", "Congenital Bronchopulmonary Leiomyosarcoma", "Congenital Pulmonary Myofibroblastic Tumor", "Congenital Mesenchymal Malformation of Lung", "Congenital peribronchial myofibroblastic tumor", "Congenital Peribronchial Myofibroblastic Tumor", "Congenital peribronchial myofibroblastic tumour", "Myofibroblastic tumor, peribronchial (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Peribronchial Myofibroblastic Tumor", "shortest_name_length": 23}
{"curie": "MONDO:0016579", "names": ["dominant hypophosphatemia with nephrolithiasis or osteoporosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dominant hypophosphatemia with nephrolithiasis or osteoporosis", "shortest_name_length": 62}
{"curie": "MONDO:0006541", "names": ["EB", "Fox disease", "Acanthosis bullosa", "Acantholysis bullosa", "acantholysis bullosa", "ACANTHOLYSIS BULLOSA", "Acantholysis Bullosa", "bullosa epidermolysis", "EPIDERMOLYSIS BULLOSA", "epidermolysis bullosa", "Epidermolysis bullosa", "Epidermolysis Bullosa", "epidermolysis; bullosa", "bullosa; epidermolysis", "EB - Epidermolysis bullosa", "Bullous recurrent eruption", "Epidermolysis bullosa, NOS", "Dermatitis bullosa hereditaria", "Keratolysis bullosa hereditaria", "Epidermolysis bullosa (disorder)", "epidermolysis bullosa (diagnosis)", "Epidermolysis bullosa, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolysis bullosa", "shortest_name_length": 2}
{"curie": "MONDO:0100211", "names": ["GHISID1", "Laron-like syndrome", "Laron type dwarfism 2", "Laron syndrome type 2", "Laron syndrome with immunodeficiency", "Short stature due to STAT5b deficiency", "short stature due to STAT5b deficiency", "Laron syndrome due to postreceptor defect", "LARON SYNDROME DUE TO POSTRECEPTOR DEFECT", "Laron syndrome with immunodeficiency (disorder)", "growth hormone insensitivity with immunodeficiency", "Growth Hormone Insensitivity With Immunodeficiency", "GROWTH HORMONE INSENSITIVITY DUE TO POSTRECEPTOR DEFECT", "growth hormone insensitivity due to postreceptor defect", "Growth Hormone Insensitivity Due To Postreceptor Defect", "growth hormone insensitivity syndrome with immune dysregulation 1", "growth hormone insensitivity with immune dysregulation 1, autosomal recessive", "GROWTH HORMONE INSENSITIVITY SYNDROME WITH IMMUNE DYSREGULATION 1, AUTOSOMAL RECESSIVE", "Short stature due to STAT5b (signal transducer and activator of transcription 5b) deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "growth hormone insensitivity with immune dysregulation 1, autosomal recessive", "shortest_name_length": 7}
{"curie": "MONDO:0100114", "names": ["dry AMD", "dry ARMD", "dry age related macular degeneration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dry age related macular degeneration", "shortest_name_length": 7}
{"curie": "UMLS:C4521735", "names": ["Stage IV Esophageal Squamous Cell Cancer", "Postneoadjuvant Therapy Stage IV Esophageal Squamous Cell Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postneoadjuvant Therapy Stage IV Esophageal Squamous Cell Carcinoma AJCC v8", "shortest_name_length": 40}
{"curie": "MONDO:0001509", "names": ["TED", "Graves eye disease", "Graves Orbitopathy", "Graves Eye Disease", "Graves’ orbitopathy", "Graves’ eye disease", "thyroid eye disease", "Orbitopathy, Graves", "thyroid orbitopathy", "Eye Disease, Graves", "Graves' eye disease", "eye thyroid disease", "Disease, Graves Eye", "Thyroid orbitopathy", "Thyroid eye disease", "Thyroid Eye Disease", "Thyroid Eye Diseases", "Disease, Thyroid Eye", "grave ophthalmopathy", "Eye Disease, Thyroid", "Graves ophthalmopathy", "Endocrine orbitopathy", "graves ophthalmopathy", "Graves Ophthalmopathy", "Exophthalmos endocrine", "Graves’ ophthalmopathy", "Thyroid ophthalmopathy", "endocrine exophthalmos", "dysthyroid eye disease", "Ophthalmopathy, Graves", "Dysthyroid orbitopathy", "Dysthyroid eye disease", "Endocrine exophthalmos", "Graves' ophthalmopathy", "graves' ophthalmopathy", "Dysthyroid exophthalmos", "Endocrine ophthalmopathy", "Dysthyroid Ophthalmopathy", "Ophthalmic Graves disease", "Dysthyroid ophthalmopathy", "Ophthalmopathy, Dysthyroid", "Endocrine exophthalmos, NOS", "Dysthyroid Ophthalmopathies", "Thyroid eye disease (disorder)", "thyroid-associated ophthalmopathy", "Thyroid-associated ophthalmopathy", "Thyroid-Associated Ophthalmopathy", "associated ophthalmopathy thyroid", "Thyroid Associated Ophthalmopathy", "endocrine exophthalmos (diagnosis)", "Thyroid associated opthalmopathies", "Graves' ophthalmopathy (diagnosis)", "Ophthalmopathy, Thyroid Associated", "Ophthalmopathy, Thyroid-Associated", "Thyroid-Associated Ophthalmopathies", "Thyroid Associated Ophthalmopathies", "Ophthalmopathies, Thyroid-Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endocrine exophthalmos", "shortest_name_length": 3}
{"curie": "MONDO:0014886", "names": ["MRT55", "NEDMIGS", "MRT55, FORMERLY", "mental retardation, autosomal recessive 55", "mental retardation, autosomal recessive type 55", "intellectual disability, autosomal recessive 55", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 55, FORMERLY", "intellectual disability, autosomal recessive type 55", "neurodevelopmental disorder with microcephaly and gray sclerae", "NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY AND GRAY SCLERAE", "severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C1514839", "names": ["Renal Cell Carcinoma Associated with t(X;1)(p11.2;q21)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal Cell Carcinoma Associated with t(X;1)(p11.2;q21)", "shortest_name_length": 54}
{"curie": "UMLS:C4683232", "names": ["Clinical Stage I Retinoblastoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage I Retinoblastoma AJCC v8", "shortest_name_length": 39}
{"curie": "MONDO:0100343", "names": ["antenatal Bartter syndrome", "hyperprostaglandin E syndrome", "Bartter syndrome, furosemide type", "Bartter syndrome, furosemide-amiloride type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "antenatal Bartter syndrome", "shortest_name_length": 26}
{"curie": "UMLS:C1135745", "names": ["Serogroup A Meningococcal Meningitis", "Meningococcal Meningitis, Serogroup A", "Meningitis, Meningococcal, Serogroup A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meningitis, Meningococcal, Serogroup A", "shortest_name_length": 36}
{"curie": "MONDO:0016360", "names": ["marcothrombocytopenia with mitral valve insufficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "marcothrombocytopenia with mitral valve insufficiency", "shortest_name_length": 53}
{"curie": "MONDO:0015764", "names": ["mosaic trisomy 20", "Mosaic trisomy type 20", "Mosaic trisomy chromosome 20"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mosaic trisomy 20", "shortest_name_length": 17}
{"curie": "UMLS:C1514800", "names": ["Rectal Cancer by Astler-Coller Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rectal Cancer by Astler-Coller Stage", "shortest_name_length": 36}
{"curie": "MONDO:0001056", "names": ["stomach ca", "gastric cancer", "Gastric cancer", "GASTRIC CANCER", "Gastric Cancer", "stomach cancer", "Stomach Cancer", "Stomach cancer", "Stomach Cancers", "stomach cancers", "Stomach--Cancer", "Gastric Cancers", "Cancer, Stomach", "Cancer, Gastric", "gastric cancers", "Cancers, Gastric", "Cancers, Stomach", "gastric neoplasm", "Cancer of Stomach", "cancer of stomach", "Ca body - stomach", "Ca Body - stomach", "Cancer of stomach", "Gastric cancer NOS", "Gastric malignancy", "cancer of the stomach", "Cancer of the Stomach", "Neoplasm malig;stomach", "CA - Cancer of stomach", "Malignant Gastric Tumor", "malignant gastric tumor", "gastric cancer, somatic", "Malignant gastric tumor", "Stomach (gastric) cancer", "malignant tumor of stomach", "GASTRIC CANCER, INTESTINAL", "gastric cancer (diagnosis)", "gastric cancer, intestinal", "Malignant Gastric Neoplasm", "Malignant neoplasm stomach", "malignant stomach neoplasm", "Malignant Tumor of Stomach", "Malignant tumor of stomach", "malignant gastric neoplasm", "Malignant tumour of stomach", "Ca lesser curvature - stomach", "Malignant Neoplasm of Stomach", "malignant neoplasm of stomach", "Malignant neoplasm of stomach", "malignant tumor of the stomach", "Malignant Tumor of the Stomach", "Ca greater curvature - stomach", "ca greater curvature of stomach", "malignant neoplasm of the stomach", "Malignant Neoplasm of the Stomach", "malignant neosplasm of the stomach", "malignant tumor of body of stomach", "Malignant tumor of body of stomach", "Malignant neoplasm of stomach, NOS", "Malignant tumour of body of stomach", "Malignant neoplasm of body of stomach", "malignant neoplasm of body of stomach", "Malignant tumor of stomach (disorder)", "malignant neoplasm of stomach (diagnosis)", "malignant tumor of lesser curve of stomach", "Malignant tumor of lesser curve of stomach", "Malignant neoplasm of stomach, unspecified", "Malignant tumor of greater curve of stomach", "malignant tumor of greater curve of stomach", "Malignant tumour of lesser curve of stomach", "Malignant tumour of greater curve of stomach", "Malignant tumor of body of stomach (disorder)", "gastric cancer risk after h. pylori infection", "malignant neoplasm of lesser curve of stomach", "malignant tumor of lesser curvature of stomach", "malignant tumor of greater curvature of stomach", "Malignant neoplasm of stomach, unspecified site", "malignant neoplasm of body of stomach (diagnosis)", "malignant neoplasm of lesser curvature of stomach", "malignant neoplasm of greater curvature of stomach", "Malignant tumor of lesser curve of stomach (disorder)", "Malignant tumor of greater curve of stomach (disorder)", "Malignant neoplasm of lesser curvature of stomach, NOS", "Malignant neoplasm of greater curvature of stomach, NOS", "malignant neoplasm of lesser curvature of stomach (diagnosis)", "malignant neoplasm of greater curvature of stomach (diagnosis)", "Malignant neoplasm of lesser curvature of stomach, unspecified", "Malignant neoplasm of greater curvature of stomach, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric cancer", "shortest_name_length": 10}
{"curie": "UMLS:C3900107", "names": ["Acute Placental Infact", "Acute Placental Infarct", "Acute Placental Infarction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Placental Infarction", "shortest_name_length": 22}
{"curie": "UMLS:C2931207", "names": ["Usher syndrome type 1C", "Usher syndrome, type 1C", "Usher syndrome, Acadian variety", "Usher syndrome type 1C (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Usher syndrome, type 1C", "shortest_name_length": 22}
{"curie": "MONDO:0021918", "names": ["arena syndrome", "Arena syndrome", "Spastic paraplegia with iron deposits in basal ganglia", "spastic paraplegia with iron deposits in basal ganglia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arena syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0013519", "names": ["DKCB2", "autosomal recessive dyskeratosis congenita 2", "Dyskeratosis Congenita, Autosomal Recessive 2", "dyskeratosis congenita, autosomal recessive 2", "DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 2", "dyskeratosis congenita, autosomal recessive type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyskeratosis congenita, autosomal recessive 2", "shortest_name_length": 5}
{"curie": "MONDO:0013070", "names": ["MIAR", "SPGF7", "SPERMATOGENIC FAILURE 7", "spermatogenic failure 7", "Spermatogenic Failure 7", "spermatogenic failure type 7", "Male infertility, nonsyndromic, autosomal recessive", "MALE INFERTILITY, NONSYNDROMIC, AUTOSOMAL RECESSIVE", "Male Infertility, Nonsyndromic, Autosomal Recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 7", "shortest_name_length": 4}
{"curie": "MONDO:0017535", "names": ["mirror hand, unilateral", "central polydactyly of fingers, unilateral", "mesoaxial polydactyly of fingers, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central polydactyly of fingers, unilateral", "shortest_name_length": 23}
{"curie": "UMLS:C0854719", "names": ["Corneal Touch", "Corneal touch"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Corneal touch", "shortest_name_length": 13}
{"curie": "MONDO:0014789", "names": ["CDG2O", "CDGIIo", "CDGIIdo", "CDG IIo", "CDG-IIo", "CCDC115-CDG", "CDG syndrome type IIo", "Congenital disorder of glycosylation type 2o", "CCDC115 congenital disorder of glycosylation", "congenital disorder of glycosylation type 2o", "congenital disorder of glycosylation type IIo", "Congenital disorder of glycosylation type IIo", "congenital disorder of glycosylation, type IIo", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIo", "Carbohydrate deficient glycoprotein syndrome type IIo", "carbohydrate deficient glycoprotein syndrome type IIo", "Coiled-coil domain containing 115 congenital disorder of glycosylation", "Coiled-coil domain containing 115 congenital disorder of glycosylation (disorder)", "CCDC115-CDG - coiled-coil domain containing 115 congenital disorder of glycosylation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CCDC115-CDG", "shortest_name_length": 5}
{"curie": "UMLS:C4683578", "names": ["Lugano Classification Stage II Adult Non-Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Stage II Adult Non-Hodgkin Lymphoma AJCC v8", "shortest_name_length": 65}
{"curie": "MONDO:0008916", "names": ["CARDIOMYOPATHY ASSOCIATED WITH MYOPATHY AND SUDDEN DEATH", "cardiomyopathy associated with myopathy and sudden death", "Cardiomyopathy Associated With Myopathy And Sudden Death"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiomyopathy associated with myopathy and sudden death", "shortest_name_length": 56}
{"curie": "UMLS:C4521650", "names": ["II", "Stage II Esophageal Adenocarcinoma", "Pathologic Stage II Esophageal Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage II Esophageal Adenocarcinoma AJCC v8", "shortest_name_length": 2}
{"curie": "MONDO:0003079", "names": ["mastocytoma", "Mastocytoma", "Mastocytoma NOS", "Mastocytoma, NOS", "Mastocytoma (disorder)", "mastocytoma (diagnosis)", "Mastocytoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mastocytoma", "shortest_name_length": 11}
{"curie": "MONDO:0002861", "names": ["testis sarcoma", "Sarcoma of Testis", "sarcoma of testis", "testicular sarcoma", "Testicular Sarcoma", "sarcoma of the testis", "Sarcoma of the Testis", "sarcoma of testis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testis sarcoma", "shortest_name_length": 14}
{"curie": "MONDO:0011674", "names": ["Cmt2m", "CMT2M", "Cmtdi1", "CMTDIB", "CMTDI1", "Di-CMTB", "DI-CMTB", "DNM2 Charcot-Marie-Tooth disease", "Charcot-Marie-Tooth disease, axonal type 2M", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2M", "Charcot-Marie-Tooth disease, axonal, type 2M", "Charcot-Marie-Tooth Disease, Axonal, Type 2m", "Charcot-Marie-Tooth Neuropathy, Axonal, Type 2m", "Charcot-Marie-Tooth neuropathy, axonal, type 2M", "CHARCOT-MARIE-TOOTH NEUROPATHY, AXONAL, TYPE 2M", "Charcot-Marie-Tooth disease dominant intermediate B", "Charcot-Marie-Tooth disease, dominant intermediate B", "Charcot-Marie-Tooth Disease, Dominant Intermediate B", "CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B", "Charcot-Marie-Tooth neuropathy dominant intermediate B", "Charcot-Marie-Tooth disease caused by mutation in DNM2", "Charcot-Marie-Tooth neuropathy, dominant Intermediate B", "Charcot-Marie-Tooth Neuropathy, Dominant Intermediate B", "CHARCOT-MARIE-TOOTH NEUROPATHY, DOMINANT INTERMEDIATE B", "Charcot-Marie-Tooth disease dominant intermediate type B", "DNM2-related intermediate Charcot-Marie-Tooth neuropathy", "Charcot-Marie-Tooth disease, dominant Intermediate type B", "CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B (disorder)", "Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2m", "Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2M", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2M", "autosomal dominant intermediate Charcot-Marie-Tooth disease type B", "Autosomal dominant intermediate Charcot-Marie-Tooth disease type B", "Charcot-Marie-Tooth disease autosomal dominant intermediate type B", "Charcot-Marie-Tooth disease, dominant Intermediate B, with neutropenia", "CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B, WITH NEUTROPENIA", "Charcot-Marie-Tooth Disease, Dominant Intermediate B, With Neutropenia", "Charcot-Marie-Tooth Neuropathy, Dominant Intermediate B, with Neutropenia", "CHARCOT-MARIE-TOOTH NEUROPATHY, DOMINANT INTERMEDIATE B, WITH NEUTROPENIA", "Charcot-Marie-Tooth neuropathy, dominant Intermediate B, with neutropenia", "Autosomal dominant intermediate Charcot-Marie-Tooth disease type B (disorder)", "Autosomal dominant intermediate Charcot-Marie-Tooth disease type B (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease dominant intermediate B", "shortest_name_length": 5}
{"curie": "UMLS:C5239547", "names": ["Unresectable Epithelioid Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Epithelioid Sarcoma", "shortest_name_length": 32}
{"curie": "MONDO:0004085", "names": ["choroid epithelioid cell melanoma", "Choroid Epithelioid Cell Melanoma", "Choroidal Epithelioid Cell Melanoma", "Choroidal epithelioid cell melanoma", "choroidal epithelioid cell melanoma", "Epithelioid Cell Melanoma of Choroid", "epithelioid cell melanoma of choroid", "optic choroid epithelioid cell melanoma", "Epithelioid Cell Melanoma of the Choroid", "epithelioid cell melanoma of the choroid", "epithelioid cell melanoma of optic choroid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choroid epithelioid cell melanoma", "shortest_name_length": 33}
{"curie": "UMLS:C0268562", "names": ["T-protein deficiency", "T protein deficiency", "Aminomethyltransferase deficiency", "Type II Nonketotic Hyperglycinemia", "Non-ketotic hyperglycinemia type II", "Nonketotic Hyperglycinemia, Type II", "Nonketotic hyperglycinemia, type II", "Nonketotic hyperglycinaemia, type II", "Hyperglycinemia, Nonketotic, Type II", "Non-ketotic hyperglycinaemia type II", "Aminomethyltransferase deficiency (disorder)", "Non-ketotic hyperglycinemia T protein deficiency", "Non-ketotic hyperglycinaemia T protein deficiency", "Tetrahydrofolate aminomethyltransferase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyperglycinemia, Nonketotic, Type II", "shortest_name_length": 20}
{"curie": "UMLS:C4331329", "names": ["Stage III Nasopharyngeal Throat Cancer", "Stage III Nasopharyngeal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Nasopharyngeal Carcinoma AJCC v8", "shortest_name_length": 38}
{"curie": "MONDO:0001423", "names": ["drug-induced mental disorder", "Other specified drug-induced mental disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "drug-induced mental disorder", "shortest_name_length": 28}
{"curie": "UMLS:C0334455", "names": ["Periosteal Fibroma", "Periosteal fibroma", "Periosteal fibroma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Periosteal fibroma", "shortest_name_length": 18}
{"curie": "MONDO:0004723", "names": ["Liver Leiomyoma", "liver leiomyoma", "Hepatic Leiomyoma", "hepatic leiomyoma", "Leiomyoma of Liver", "leiomyoma of liver", "leiomyoma of the liver", "Leiomyoma of the Liver", "leiomyoma of the Liver"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "liver leiomyoma", "shortest_name_length": 15}
{"curie": "MONDO:0013877", "names": ["MPYCD", "MITOCHONDRIAL PYRUVATE CARRIER DEFICIENCY", "mitochondrial pyruvate carrier deficiency", "Mitochondrial pyruvate carrier deficiency", "Mitochondrial pyruvate carrier deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial pyruvate carrier deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C0919938", "names": ["Anastomotic stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anastomotic stenosis", "shortest_name_length": 20}
{"curie": "UMLS:C4521653", "names": ["III", "Stage III Esophageal Adenocarcinoma", "Pathologic Stage III Esophageal Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage III Esophageal Adenocarcinoma AJCC v8", "shortest_name_length": 3}
{"curie": "UMLS:C0749225", "names": ["SYSTOLIC DYSFUNCTION", "Systolic dysfunction", "systolic dysfunction", "Systolic dysfunction (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Systolic dysfunction", "shortest_name_length": 20}
{"curie": "MONDO:0030314", "names": ["IBD31", "INFLAMMATORY BOWEL DISEASE, EARLY-ONSET, AUTOSOMAL RECESSIVE", "inflammatory bowel disease, early-onset, autosomal recessive", "inflammatory bowel disease (infantile ulcerative colitis) 31", "inflammatory bowel disease (infantile ulcerative colitis) 31, autosomal recessive", "INFLAMMATORY BOWEL DISEASE (INFANTILE ULCERATIVE COLITIS) 31, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory bowel disease (infantile ulcerative colitis) 31, autosomal recessive", "shortest_name_length": 5}
{"curie": "UMLS:C0751123", "names": ["Atonic Absence Seizure", "Atonic Absence Seizures", "Seizure, Atonic Absence", "Absence Seizure, Atonic", "Absence Seizures, Atonic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atonic Absence Seizures", "shortest_name_length": 22}
{"curie": "MONDO:0019803", "names": ["angioma serpiginosum", "Angioma serpiginosum", "Angioma Serpiginosum", "serpiginosum; angioma", "angioma; serpiginosum", "essential telangiectasia", "Essential telangiectasia", "essential telangiectasias", "Angioma serpiginosum of skin", "angioma serpiginosum of skin", "Angioma serpiginosum (disorder)", "angioma serpiginosum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angioma serpiginosum", "shortest_name_length": 20}
{"curie": "UMLS:C0401160", "names": ["Chemotherapy sickness", "Chemotherapy induced vomiting", "chemotherapy induced nausea vomiting", "chemotherapy-induced nausea and vomiting", "Chemotherapy-induced nausea and vomiting", "Chemotherapy-Induced Nausea and Vomiting", "nausea with vomiting chemotherapy-induced", "Chemotherapy-related nausea and/or vomiting", "Chemotherapy-Related Nausea and/or Vomiting", "Chemotherapy-induced nausea and vomiting (symptom)", "Chemotherapy-induced nausea and vomiting (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chemotherapy-induced nausea and vomiting", "shortest_name_length": 21}
{"curie": "MONDO:0014125", "names": ["SYM1B", "proximal symphalangism 2", "SYMPHALANGISM, PROXIMAL, 1B", "symphalangism, proximal, 1B", "symphalangism, proximal, type 1B", "GDF5 proximal symphalangism (disease)", "proximal symphalangism (disease) caused by mutation in GDF5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "symphalangism, proximal, 1B", "shortest_name_length": 5}
{"curie": "MONDO:0003395", "names": ["testis granulosa cell tumor", "Granulosa Cell Tumor of Testis", "granulosa cell tumor of testis", "Granulosa cell tumor of testis", "Testicular Granulosa Cell Tumor", "Granulosa cell tumour of testis", "testicular granulosa cell tumor", "testicular granulosa cell tumour", "granulosa cell neoplasm of testis", "Granulosa Cell Neoplasm of Testis", "granulosa cell tumor of the testis", "testicular granulosa cell neoplasm", "Testicular Granulosa Cell Neoplasm", "Granulosa cell tumor of the testis", "Granulosa Cell Tumor of the Testis", "Granulosa cell tumour of the testis", "Granulosa Cell Neoplasm of the Testis", "granulosa cell neoplasm of the testis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular granulosa cell tumor", "shortest_name_length": 27}
{"curie": "UMLS:C1142162", "names": ["Injection site scar", "Injection site scar (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site scar", "shortest_name_length": 19}
{"curie": "MONDO:0011439", "names": ["SCA12", "Spinocerebellar Ataxia 12", "spinocerebellar ataxia 12", "SPINOCEREBELLAR ATAXIA 12", "spinocerebellar ataxia type 12", "Spinocerebellar ataxia type 12", "Spinocerebellar Ataxia Type 12", "SCA12 Spinocerebellar Ataxia 12", "Spinocerebellar ataxia type 12 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia type 12", "shortest_name_length": 5}
{"curie": "MONDO:0001341", "names": ["SIgAD", "Decreased IgA", "IgA deficiency", "iga deficiency", "IgA Deficiency", "Deficiency, IgA", "deficiency, IgA", "IgA deficiencies", "IgA Deficiencies", "iga deficiencies", "Deficiencies, IgA", "deficiencies, IgA", "Reduced IgA levels", "selective IgA deficiency", "iga selective deficiency", "deficiency iga selective", "Selective IgA deficiency", "IGA DEFICIENCY, ISOLATED", "selective iga deficiency", "IGA DEFICIENCY, SELECTIVE", "Decreased immunoglobulin A", "deficiencies immunoglobulin", "immunoglobulin A deficiency", "Immunoglobulin A deficiency", "immunoglobulin a deficiency", "gamma-A-globulin deficiency", "Gamma-A globulin deficiency", "IgA, SELECTIVE DEFICIENCY OF", "immunodeficiency selective iga", "Low levels of immunoglobulin A", "Selective IgA immunodeficiency", "Selective IgA Immunodeficiency", "selective IgA immunodeficiency", "Decreased circulating IgA level", "immunoglobulin alpha deficiency", "selective IgA deficiency disease", "selective IgA deficiency (diagnosis)", "selective immunoglobulin A deficiency", "Selective immunoglobulin A deficiency", "Immunoglobulin A deficiency (disorder)", "immunoglobulin; deficiency IgA selective", "IMMUNOGLOBULIN A, SELECTIVE DEFICIENCY OF", "Selective deficiency of immunoglobulin A [IgA]", "Selective immunoglobulin A deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "selective IgA deficiency disease", "shortest_name_length": 5}
{"curie": "UMLS:C0521498", "names": ["Injection site irritation", "Injection site irritation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site irritation", "shortest_name_length": 25}
{"curie": "MONDO:0007630", "names": ["NCMD", "caped", "CAPED", "MCDR1", "CAPE dystrophy", "retinal macular dystrophy 1", "Retinal Macular Dystrophy-1", "Progressive foveal dystrophy", "progressive foveal dystrophy", "foveal dystrophy progressive", "Macular Dystrophy, Retinal, 1", "foveal dystrophy, progressive", "Foveal dystrophy, progressive", "North Carolina macular dystrophy", "NORTH CAROLINA MACULAR DYSTROPHY", "North carolina macular dystrophy", "North Carolina Macular Dystrophy", "North Carolina retinal dystrophy", "FOVEAL DYSTROPHY, PROGRESSIVE, FORMERLY", "foveal dystrophy, progressive, formerly", "macular dystrophy 1, North Carolina type", "North Carolina macular dystrophy, retinal 1", "North Carolina macular dystrophy (disorder)", "central retinal pigment epithelial dystrophy", "Central retinal pigment epithelial dystrophy", "central areolar pigment epithelial dystrophy", "Central areolar pigment epithelial dystrophy", "retinal pigment epithelial dystrophy central", "CENTRAL AREOLAR PIGMENT EPITHELIAL DYSTROPHY", "North Carolina retinal dystrophy (diagnosis)", "retinal pigment epithelial dystrophy, central", "Retinal pigment epithelial dystrophy, central", "RETINAL PIGMENT EPITHELIAL DYSTROPHY, CENTRAL", "macular dystrophy retinal 1 North Carolina type", "MACULAR DYSTROPHY, RETINAL, 1, NORTH CAROLINA TYPE", "Macular dystrophy, retinal, 1, North Carolina type", "macular dystrophy, retinal, 1, NORTH Carolina type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "North Carolina macular dystrophy", "shortest_name_length": 4}
{"curie": "MONDO:0012212", "names": ["LDS1", "AAT5", "Furlong syndrome", "FURLONG SYNDROME", "Loeys-Dietz syndrome 1", "LOEYS-DIETZ SYNDROME 1", "TGFBR1 Loeys-Dietz syndrome", "Loeys-Dietz syndrome type 1", "Loeys-Dietz Syndrome Type 1", "Loeys-Dietz syndrome type 1a", "Loeys-Dietz syndrome type 2a", "Loeys-Dietz Syndrome, Type 1a", "Loeys-Dietz Syndrome, Type 2A", "Loeys Dietz Syndrome, Type 1a", "familial throacic aortic aneurysm 5", "Loeys-Dietz Aortic Aneurysm Syndrome", "aortic aneurysm, familial thoracic 5", "Aortic Aneurysm, Familial Thoracic 5", "AORTIC ANEURYSM, FAMILIAL THORACIC 5", "Loeys-Dietz aortic aneurysm syndrome", "Loeys Dietz Aortic Aneurysm Syndrome", "LOEYS-DIETZ AORTIC ANEURYSM SYNDROME", "Loeys-Dietz syndrome type 2a (diagnosis)", "Loeys-Dietz syndrome type 1a (diagnosis)", "Marfanoid disorder with craniosynostosis, type 2", "Loeys-Dietz syndrome caused by mutation in TGFBR1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Loeys-Dietz syndrome 1", "shortest_name_length": 4}
{"curie": "MONDO:0014507", "names": ["CATMANS", "Catel-Manzke syndrome", "Catel-Manzke Syndrome", "CATEL-MANZKE SYNDROME", "Catel Manzke syndrome", "micrognathia digital syndrome", "MICROGNATHIA DIGITAL SYNDROME", "Micrognathia digital syndrome", "Catel Manzke syndrome (disorder)", "Palatodigital syndrome Catel-Manzke type", "PALATODIGITAL SYNDROME, CATEL-MANZKE TYPE", "Palatodigital syndrome, Catel-Manzke type", "index finger anomaly-Pierre Robin syndrome", "Index finger anomaly-Pierre Robin syndrome", "index finger anomaly with Pierre Robin syndrome", "INDEX FINGER ANOMALY WITH PIERRE ROBIN SYNDROME", "Index Finger Anomaly With Pierre Robin Syndrome", "Pierre Robin syndrome with hyperphalangy and clinodactyly", "Pierre Robin sequence-hyperphalangy-clinodactyly syndrome", "Pierre Robin syndrome-hyperphalangy-clinodactyly syndrome", "PIERRE ROBIN SYNDROME WITH HYPERPHALANGY AND CLINODACTYLY", "hyperphalangy-clinodactyly of index finger with Pierre Robin syndrome", "HYPERPHALANGY-CLINODACTYLY OF INDEX FINGER WITH PIERRE ROBIN SYNDROME", "Hyperphalangy-clinodactyly of index finger with Pierre Robin syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Catel-Manzke syndrome", "shortest_name_length": 7}
{"curie": "UMLS:C0271574", "names": ["Ferrier-Stone syndrome", "Primary empty sella syndrome", "Primary Empty Sella Syndrome", "Empty Sella Syndrome, Primary", "Abnormal sella turcica syndrome", "Familial absence of sella turcica", "Pituitary dwarfism with small sella turcica", "Pituitary dwarfism with small sella turcica (disorder)", "Familial panhypopituitarism with abnormal sella turcica"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Empty Sella Syndrome, Primary", "shortest_name_length": 22}
{"curie": "MONDO:0044714", "names": ["MMYAT", "MYOPATHY, MITOCHONDRIAL, AND ATAXIA", "myopathy, mitochondrial, and ataxia", "Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome", "mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome", "Mitochondrial myopathy-cerebellar atrophy-pigmentary retinopathy syndrome", "mitochondrial myopathy-cerebellar atrophy-pigmentary retinopathy syndrome", "Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome", "Mitochondrial myopathy, cerebellar atrophy, pigmentary retinopathy syndrome", "Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0001327", "names": ["Pelvic muscle wasting", "pelvic muscle wasting", "pelvic muscle wasting (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pelvic muscle wasting", "shortest_name_length": 21}
{"curie": "UMLS:C5556295", "names": ["Advanced Microsatellite Stable Endometrial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Microsatellite Stable Endometrial Carcinoma", "shortest_name_length": 52}
{"curie": "UMLS:C4687629", "names": ["Mediastinal Epithelioid Hemangioendothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mediastinal Epithelioid Hemangioendothelioma", "shortest_name_length": 44}
{"curie": "MONDO:0005575", "names": ["CRC", "colon cancer", "colorectum cancer", "colorectal cancer", "large bowel cancer", "cancer of colorectum", "of large bowel cancer", "colon cancer, somatic", "cancer of large bowel", "cancer of large colon", "Cancer of large bowel", "large intestine cancer", "cancer intestine large", "cancer intestines large", "Cancer of large intestine", "cancer of large intestine", "cancer of the large bowel", "Malignant Colorectal Tumor", "malignant colorectal tumor", "colorectal cancer, somatic", "Neoplasm malig;bowel;large", "CA - Cancer of large bowel", "malignant large bowel tumor", "Malignant Large Bowel Tumor", "malignant colorectum neoplasm", "malignant colorectal neoplasm", "Malignant Colorectal Neoplasm", "malignant tumor of large bowel", "malignant large bowel neoplasm", "Colorectal neoplasms malignant", "Malignant Tumor of Large Bowel", "Neoplasm malig;intestine;large", "Malignant Large Bowel Neoplasm", "malignant large intestine tumor", "colon cancer, advanced, somatic", "Malignant Large Intestine Tumor", "malignant neoplasm of colorectum", "malignant neoplasm of large bowel", "Malignant Neoplasm of Large Bowel", "Malignant Large Intestine Neoplasm", "Malignant Tumor of Large Intestine", "malignant large intestine neoplasm", "Malignant Tumor of the Large Bowel", "malignant tumor of large intestine", "Malignant tumor of large intestine", "large intestine cancer (diagnosis)", "malignant tumor of the large bowel", "Malignant tumour of large intestine", "malignant neoplasm of large intestine", "malignant neoplasm of the large bowel", "Malignant Neoplasm of Large Intestine", "Malignant neoplasm of large intestine", "Malignant Neoplasm of the Large Bowel", "Malignant Tumor of the Large Intestine", "malignant neosplasm of the large bowel", "malignant tumor of the large intestine", "Malignant large intestinal neoplasm NOS", "Malignant neoplasm of large intestine NOS", "Malignant Neoplasm of the Large Intestine", "malignant neoplasm of the large intestine", "Malignant neoplasm of large intestine, NOS", "malignant neosplasm of the large intestine", "Malignant tumor of large intestine (disorder)", "malignant neoplasm of large intestine (diagnosis)", "colorectal cancer, autosomal dominant, somatic mutation", "colorectal cancer with chromosomal instability, somatic", "colon cancer, susceptibility to, autosomal dominant, somatic mutation", "colorectal cancer, susceptibility to, autosomal dominant, somatic mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorectal cancer", "shortest_name_length": 3}
{"curie": "MONDO:0011182", "names": ["TMAU", "TMAuria", "Trimethylaminuria", "trimethylaminuria", "TRIMETHYLAMINURIA", "fish-odor syndrome", "fish odor syndrome", "Fish-Odor Syndrome", "Fish odor syndrome", "FISH-ODOR SYNDROME", "stale fish syndrome", "Stale Fish Syndrome", "fish odour syndrome", "Fish odour syndrome", "Fish malodor syndrome", "fish malodor syndrome", "trimethylaminuria (disease)", "Trimethylaminuria (disorder)", "trimethylaminuria (diagnosis)", "High urine trimethylamine levels"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trimethylaminuria", "shortest_name_length": 4}
{"curie": "MONDO:0024635", "names": ["small bowel disease", "bowels disease small", "bowel diseases small", "Disease of small bowel", "small intestine disease", "small intestine disorder", "disease intestines small", "diseases intestine small", "Small Intestine Disorders", "disorders intestine small", "diseases intestines small", "disease of small intestine", "Disease of small intestine", "disorder of small intestine", "Disorder of small intestine", "small intestine disease or disorder", "disease or disorder of small intestine", "Disorder of small intestine (disorder)", "Diseases and Syndromes of Small Intestine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small intestine disorder", "shortest_name_length": 19}
{"curie": "MONDO:0009947", "names": ["GSSD", "5-oxoprolinuria", "pyroglutamic aciduria", "glutathione synthetase deficiency", "glutatione synthetase deficiency with 5-oxoprolinuria", "glutathione synthetase deficiency with 5-oxoprolinuria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glutathione synthetase deficiency with 5-oxoprolinuria", "shortest_name_length": 4}
{"curie": "MONDO:0022338", "names": ["ALK+ histiocytosis", "anaplastic lymphoma kinase positive histiocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ALK+ histiocytosis", "shortest_name_length": 18}
{"curie": "UMLS:C0852879", "names": ["Pulmonary alveolar bleeding", "Pulmonary alveolar hemorrhage", "Pulmonary Alveolar Hemorrhage", "Pulmonary alveolar haemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pulmonary Alveolar Hemorrhage", "shortest_name_length": 27}
{"curie": "MONDO:0003999", "names": ["Juvenile pilocytic astrocytoma", "juvenile pilocytic astrocytoma", "Juvenile Pilocytic Astrocytoma", "Pilocytic Astrocytoma, Juvenile", "Juvenile Pilocytic Astrocytomas", "Astrocytoma, Juvenile Pilocytic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile pilocytic astrocytoma", "shortest_name_length": 30}
{"curie": "MONDO:0014586", "names": ["CMS4B", "congenital myasthenic syndrome 4B", "congenital myasthenic syndrome type 4B", "congenital myasthenic syndrome 4B fast-channel", "CONGENITAL MYASTHENIC SYNDROME, 4B, FAST-CHANNEL", "MYASTHENIC SYNDROME, CONGENITAL, 4B, FAST-CHANNEL", "myasthenic syndrome, congenital, 4B, FAST-channel"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myasthenic syndrome 4B", "shortest_name_length": 5}
{"curie": "MONDO:0006087", "names": ["APAD", "appendix adenocarcinoma", "adenocarcinoma appendix", "Appendix Adenocarcinoma", "APPENDIX, ADENOCARCINOMA", "adenocarcinoma of appendix", "Adenocarcinoma of Appendix", "appendiceal adenocarcinoma", "Adenocarcinoma of appendix", "Appendiceal adenocarcinoma", "Appendiceal Adenocarcinoma", "adenocarcinoma of the appendix", "Adenocarcinoma of the Appendix", "APPENDIX CANCER, ADENOCARCINOMA", "vermiform appendix adenocarcinoma", "Adenocarcinoma of appendix (disorder)", "adenocarcinoma of appendix (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "appendix adenocarcinoma", "shortest_name_length": 4}
{"curie": "UMLS:C0272380", "names": ["tonsil disease", "tonsil; disease", "disorders tonsil", "disorders tonsils", "Disease of tonsils", "Disorder of tonsil", "Tonsillar disorder", "Tonsillar Disorder", "disorder of tonsil", "Disease of tonsils, NOS", "disease of palatine tonsil", "Disorder of palatine tonsil", "disorder of tonsil (diagnosis)", "Disorder of tonsil (palatine tonsil)", "Disorder of palatine tonsil (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disorder of tonsil (palatine tonsil)", "shortest_name_length": 14}
{"curie": "MONDO:0006950", "names": ["Retinal Vasculitis", "vasculitis; retina", "retina; vasculitis", "retinal vasculitis", "VASCULITIS RETINAL", "Vasculitis retinal", "RETINAL VASCULITIS", "Retinal vasculitis", "Vasculitis, Retinal", "Retinal vasculitis (disorder)", "retinal vasculitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal vasculitis", "shortest_name_length": 18}
{"curie": "UMLS:C1333428", "names": ["EBV-Related Carcinoma", "EBV Related Carcinoma", "Epstein-Barr Virus-Related Carcinoma", "Epstein-Barr Virus Related Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "EBV-Related Carcinoma", "shortest_name_length": 21}
{"curie": "UMLS:C3639958", "names": ["Retinopathy of Prematurity with Plus Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retinopathy of Prematurity with Plus Disease", "shortest_name_length": 44}
{"curie": "UMLS:C0856120", "names": ["Multiple sclerosis flare", "Multiple sclerosis relapse", "Relapsing multiple sclerosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Multiple sclerosis relapse", "shortest_name_length": 24}
{"curie": "MONDO:0011517", "names": ["Pseudohyperaldosteronism type 2", "pseudohyperaldosteronism type 2", "early-onset hypertension with exacerbation in pregnancy", "Early-onset hypertension with exacerbation in pregnancy", "Hypertension due to gain-of-function mutation in mineralocorticoid receptor", "hypertension, early-onset, autosomal dominant, with exacerbation in pregnancy", "hypertension due to gain-of-function mutations in the mineralocorticoid receptor", "Hypertension due to gain-of-function mutations in the mineralocorticoid receptor", "Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy", "HYPERTENSION, EARLY-ONSET, AUTOSOMAL DOMINANT, WITH SEVERE EXACERBATION IN PREGNANCY", "hypertension, early-onset, autosomal dominant, with Severe exacerbation in pregnancy", "hypertension, early-onset, autosomal dominant, with severe exacerbation in pregnancy", "Hypertension due to gain-of-function mutation in mineralocorticoid receptor (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudohyperaldosteronism type 2", "shortest_name_length": 31}
{"curie": "UMLS:C4725597", "names": ["Cervical Esophagus Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Esophagus Squamous Cell Carcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0001854", "names": ["lacrimal system disease", "lacrimal system disorder", "Lacrimal System Disorder", "lacrimal apparatus disease", "lachrymal system disorders", "Disorder of Lacrimal System", "disorder of lacrimal system", "Lacrimal Apparatus Disorder", "lacrimal apparatus disorder", "disease of lacrimal apparatus", "disorder of lacrimal apparatus", "lacrimal apparatus disease or disorder", "disease or disorder of lacrimal apparatus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lacrimal apparatus disorder", "shortest_name_length": 23}
{"curie": "MONDO:0012122", "names": ["MYMY3", "moyamoya disease 3", "MOYAMOYA DISEASE 3", "Moyamoya disease 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "moyamoya disease 3", "shortest_name_length": 5}
{"curie": "MONDO:0018417", "names": ["SPG60", "autosomal recessive spastic paraplegia type 60"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive spastic paraplegia type 60", "shortest_name_length": 5}
{"curie": "MONDO:0005700", "names": ["Varicella", "varicella", "VARICELLA", "Chickenpox", "chickenpox", "CHICKENPOX", "Chicken pox", "chicken pox", "CHICKEN POX", "Chicken Pox", "Varicella NOS", "Chickenpox NOS", "Varicella, NOS", "Chickenpox, NOS", "Varicella infection", "varicella infection", "Varicella (disorder)", "chicken pox infection", "Chicken Pox Infection", "Varicella (Chickenpox)", "Varicella [chickenpox]", "varicella infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chickenpox", "shortest_name_length": 9}
{"curie": "UMLS:C1135188", "names": ["critical illness myopathy", "myopathy critical illness", "Critical Illness Myopathy", "Critical illness myopathy", "critical illness myopathies", "Myopathy of critical illness", "myopathy of critical illness", "Critical illness myopathy (disorder)", "critical illness myopathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Critical illness myopathy", "shortest_name_length": 25}
{"curie": "MONDO:0003832", "names": ["Complement Deficiency", "deficiency complement", "complement deficiency", "Complement deficiency", "Complement Deficiencies", "complement deficiencies", "complement system; defect", "defect; complement system", "defects in complement system", "Complement deficiency disease", "complement deficiency disease", "complement activation disease", "Complement Deficiency Diseases", "defects in the complement system", "Defects in the complement system", "disorder of complement activation", "Complement deficiency disease, NOS", "Complement deficiency disease (disorder)", "Inherited Complement Deficiency Diseases", "Hereditary Complement Deficiency Diseases", "complement deficiency disease (diagnosis)", "defects in the complement system (diagnosis)", "immunodeficiency due to a complement cascade component deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complement deficiency", "shortest_name_length": 21}
{"curie": "MONDO:0011855", "names": ["CDA", "ACD", "GCD2", "CGD2", "GCDII", "avellino corneal dystrophy", "corneal dystrophy avellino", "AVELLINO CORNEAL DYSTROPHY", "Avellino corneal dystrophy", "granular corneal dystrophy 2", "Corneal dystrophy Avellino type", "corneal dystrophy Avellino type", "corneal dystrophy, AVELLINO type", "CORNEAL DYSTROPHY, AVELLINO TYPE", "corneal dystrophy, Avellino type", "Corneal dystrophy, Avellino type", "Corneal Dystrophy, Avellino Type", "granular corneal dystrophy type 2", "Granular corneal dystrophy type 2", "Granular corneal dystrophy type II", "granular-lattice corneal dystrophy", "granular corneal dystrophy, type 2", "Granular-lattice corneal dystrophy", "granular corneal dystrophy type II", "Granular Corneal Dystrophy, Type II", "GRANULAR CORNEAL DYSTROPHY, TYPE II", "Avellino corneal dystrophy (diagnosis)", "Granular and lattice corneal dystrophies", "granular and lattice corneal dystrophies", "COMBINED GRANULAR-LATTICE CORNEAL DYSTROPHY", "Combined Granular-Lattice Corneal Dystrophy", "combined granular-lattice corneal dystrophy", "granular-lattice (Avellino) corneal dystrophy", "combined granular-lattice corneal dystrophies", "Granular corneal dystrophy type II (disorder)", "Combined granular-lattice corneal dystrophies", "Granular-lattice (Avellino) corneal dystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "granular corneal dystrophy type II", "shortest_name_length": 3}
{"curie": "UMLS:C0023897", "names": ["Parasitic Liver Disease", "Liver Disease, Parasitic", "Disease, Parasitic Liver", "Parasitic Liver Diseases", "parasitic liver disorder", "Liver Diseases, Parasitic", "Diseases, Parasitic Liver"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liver Diseases, Parasitic", "shortest_name_length": 23}
{"curie": "UMLS:C3267050", "names": ["Chronic graft versus host disease in skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic graft versus host disease in skin", "shortest_name_length": 41}
{"curie": "MONDO:0001648", "names": ["Esophageal thrush", "candida esophagus", "ESOPHAGEAL THRUSH", "esophageal thrush", "Oesophageal thrush", "esophageal candida", "Esophageal candida", "CANDIDA ESOPHAGITIS", "candida esophagitis", "Candida Esophagitis", "esophagitis candida", "Candida esophagitis", "Oesophageal candida", "ESOPHAGITIS CANDIDA", "candidas esophageal", "monilial esophagitis", "candidal esophagitis", "candida oesophagitis", "Candida of esophagus", "Candida oesophagitis", "Monilial esophagitis", "Candidal esophagitis", "esophageal moniliasis", "Candidal oesophagitis", "Esophageal moniliasis", "candidiasis esophagus", "Candida of oesophagus", "Oesophageal moniliasis", "Esophageal Candidiasis", "esophageal candidiasis", "ESOPHAGEAL CANDIDIASIS", "candidiasis esophageal", "Esophageal candidiasis", "Oesophageal candidiasis", "Candidosis of esophagus", "oesophageal candidiasis", "Candidiasis;oesophageal", "Candidosis of oesophagus", "Candidiasis of esophagus", "Candidiasis of oesophagus", "Candidiasis of the esophagus", "candidiasis of the esophagus", "Candidiasis of the oesophagus", "esophageal candidiasis (diagnosis)", "Candidiasis of the esophagus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophageal candidiasis", "shortest_name_length": 17}
{"curie": "UMLS:C4725868", "names": ["Resectable Dedifferentiated Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Dedifferentiated Liposarcoma", "shortest_name_length": 39}
{"curie": "MONDO:0700142", "names": ["Canine Hemangiosarcoma", "canine hemangiosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canine hemangiosarcoma", "shortest_name_length": 22}
{"curie": "UMLS:C1563937", "names": ["Atherogeneses", "Atherogenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atherogenesis", "shortest_name_length": 13}
{"curie": "UMLS:C0235990", "names": ["Nipple ulcer", "ulcer of nipple", "Ulcer of nipple", "ulcer on nipple", "Nipple ulceration", "Nipple Ulceration", "NIPPLE ULCERATION", "ulcer of nipple (#___)", "Ulcer of nipple (disorder)", "ulcer of nipple (physical finding)", "ulcer of nipple (#___) (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ulcer of nipple", "shortest_name_length": 12}
{"curie": "MONDO:0003619", "names": ["salpingitis", "Oviductitis", "Salpingitis", "SALPINGITIS", "Salpingitides", "Salpingitis NOS", "Salpingitis, NOS", "oviduct; inflammation", "inflammation; oviduct", "Salpingitis (disorder)", "salpingitis (diagnosis)", "Inflammation of oviduct", "Salpingitis, unspecified", "fallopian tube inflammation", "inflammation; fallopian tube", "fallopian tube; inflammation", "inflammation of fallopian tube", "Inflammation of fallopian tube"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "salpingitis", "shortest_name_length": 11}
{"curie": "MONDO:0007443", "names": ["ACF", "Cayler syndrome", "cayler syndrome", "Cayler's syndrome", "cardiofacial syndrome", "Cardiofacial syndrome", "Asymmetric crying face", "Asymmetric crying facies", "ASYMMETRIC CRYING FACIES", "asymmetric crying facies", "Cayler cardiofacial syndrome", "CAYLER CARDIOFACIAL SYNDROME", "asymmetric crying facies (ACF)", "asymmetric crying facies familial", "familial asymmetric crying facies", "Partial unilateral facial paresis", "Asymmetrical crying face syndrome", "Isolated asymmetric crying facies", "facial paresis partial unilateral", "asymmetrical crying face syndrome", "Facial paresis partial unilateral", "isolated asymmetric crying facies", "unilateral partial facial paresis", "Asymmetric crying face association", "Facial Paresis, Partial, Unilateral", "FACIAL PARESIS, PARTIAL, UNILATERAL", "Partial unilateral facial paralysis", "facial paresis, partial, unilateral", "Hypoplasia of depressor angula oris muscle", "hypoplasia of anguli oris depressor muscle", "asymmetric crying facies (physical finding)", "depressor anguli oris muscle, hypoplasia of", "Depressor Anguli Oris Muscle, Hypoplasia Of", "DEPRESSOR ANGULI ORIS MUSCLE, HYPOPLASIA OF", "Asymmetric crying face association (disorder)", "depressor anguli oris muscle hypoplasia syndrome", "hypoplasia of anguli oris depressor muscle (HAODM)", "congenital unilateral hypoplasia of depressor anguli oris", "Congenital unilateral hypoplasia of depressor anguli oris"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital unilateral hypoplasia of depressor anguli oris", "shortest_name_length": 3}
{"curie": "MONDO:0016605", "names": ["HPPN", "HPPI", "Hops", "HOPS", "Rathbun syndrome", "RATHBUN SYNDROME", "Rathbun's syndrome", "Phosphoethanolaminuria", "Fetal hypophosphatasia", "PHOSPHOETHANOLAMINURIA", "phosphoethanolaminuria", "Foetal hypophosphatasia", "Infantile Rathbun disease", "infantile hypophosphatasia", "Infantile hypophosphatasia", "Hypophosphatasia, Infantile", "Congenital hypophosphatasia", "HYPOPHOSPHATASIA, INFANTILE", "Hypophosphatasia, infantile type", "Perinatal lethal Rathbun disease", "Infantile phosphoethanolaminuria", "perinatal lethal Rathburn disease", "Perinatal lethal hypophosphatasia", "perinatal lethal hypophosphatasia", "Hypophosphatasia, Perinatal Lethal", "HYPOPHOSPHATASIA, PERINATAL LETHAL", "hypophosphatasia, perinatal lethal", "High urine phosphoethanolamine levels", "Infantile hypophosphatasia (disorder)", "perinatal lethal phosphoethanolaminuria", "Perinatal lethal phosphoethanolaminuria", "Increased urine O-phosphoethanolamine level", "Increased level of O-phosphoethanolamine in urine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "perinatal lethal hypophosphatasia", "shortest_name_length": 4}
{"curie": "MONDO:0021158", "names": ["Epididymo-orchitis gonococcal", "Gonococcal epididymo-orchitis", "gonococcal epididymo-orchitis", "Gonococcal epididymo-orchitis (disorder)", "gonococcal epididymo-orchitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gonococcal epididymo-orchitis", "shortest_name_length": 29}
{"curie": "MONDO:0007271", "names": ["familial cutaneous collagenoma", "Familial cutaneous collagenoma", "COLLAGENOMA, FAMILIAL CUTANEOUS", "collagenoma, familial cutaneous", "Collagenoma, Familial Cutaneous", "Familial cutaneous collagenoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial cutaneous collagenoma", "shortest_name_length": 30}
{"curie": "MONDO:0016805", "names": ["isolated respiratory chain complex disorder", "isolated oxidative phosphorylation complex disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated oxidative phosphorylation complex disorder", "shortest_name_length": 43}
{"curie": "UMLS:C0521499", "names": ["Injection site pigmentation change", "Injection site pigmentation changes", "Injection site pigmentation change (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injection site pigmentation change", "shortest_name_length": 34}
{"curie": "MONDO:0001520", "names": ["Kleptomania", "kleptomania", "pathologic; stealing", "pathological stealing", "Pathological stealing", "stealing; pathological", "Kleptomania (disorder)", "kleptomania (diagnosis)", "Pathological stealing [kleptomania]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kleptomania", "shortest_name_length": 11}
{"curie": "MONDO:0013945", "names": ["CGR", "CG11", "PBD9B", "Refsum disease, adult, 2", "Refsum Disease, Adult, 2", "REFSUM DISEASE, ADULT, 2", "PEROXISOME BIOGENESIS DISORDER 9B", "peroxisome biogenesis disorder 9B", "peroxisome biogenesis disorder type 9B", "PEROXISOME BIOGENESIS DISORDER, PEX7-RELATED, ATYPICAL", "peroxisome biogenesis disorder, PEX7-related, atypical", "PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP R", "peroxisome biogenesis disorder, complementation group R", "Peroxisome Biogenesis Disorder, Complementation Group R", "peroxisome biogenesis disorder, complementation group 11", "Peroxisome Biogenesis Disorder, Complementation Group 11", "PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder 9B", "shortest_name_length": 3}
{"curie": "MONDO:0023005", "names": ["double uterus-hemivagina-renal agenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "double uterus-hemivagina-renal agenesis", "shortest_name_length": 39}
{"curie": "MONDO:0025139", "names": ["Stiff lamb disease", "White Muscle Disease", "White muscle disease", "white muscle disease", "White muscle diseases", "muscle disease, White", "Disease, White Muscle", "White Muscle Diseases", "Muscle Disease, White", "disease, White muscle", "muscle diseases, White", "Diseases, White Muscle", "Muscle Diseases, White", "diseases, White muscle", "Enzootic muscular dystrophy", "Skeletal white muscle disease", "Nutritional myopathy of lambs and calves", "Nutritional myopathy of lambs AND/OR calves", "Myopathy secondary to deficiency of selenium and/or vitamin E", "Skeletal myopathy secondary to deficiency of selenium and/or vitamin E", "Myopathy secondary to deficiency of selenium and/or vitamin E (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "white muscle disease", "shortest_name_length": 18}
{"curie": "UMLS:C0742803", "names": ["conus medullary syndrome", "Conus Medullaris Syndrome", "Conus medullaris syndrome", "CONUS MEDULLARIS SYNDROME", "conus medullaris syndrome", "Syndrome, Conus Medullaris", "conus; medullaris syndrome", "syndrome; conus medullaris", "conus medullaris; syndrome", "Conus Medullaris Syndromes", "medullaris syndrome; conus", "Syndromes, Conus Medullaris", "Conus medullaris syndrome (disorder)", "conus medullaris syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conus Medullaris Syndrome", "shortest_name_length": 24}
{"curie": "UMLS:C1262104", "names": ["Urinary tract infection pseudomonal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urinary tract infection pseudomonal", "shortest_name_length": 35}
{"curie": "MONDO:0012905", "names": ["HLD6", "HABC", "H-ABC", "hypomyelinating leukodystrophy 6", "Hypomyelinating Leukodystrophy-6", "Leukodystrophy, Hypomyelinating, 6", "leukodystrophy, hypomyelinating, 6", "LEUKODYSTROPHY, HYPOMYELINATING, 6", "hypomyelinating leukodystrophy type 6", "leukodystrophy, hypomyelinating, type 6", "hypomyelination with atrophy of basal ganglia and cerebellum", "Hypomyelination with atrophy of basal ganglia and cerebellum", "Hypomyelination with Atrophy of Basal Ganglia and Cerebellum", "H-ABC - hypomyelination, atrophy of basal ganglia and cerebellum", "Hypomyelination with atrophy of basal ganglia and cerebellum syndrome", "Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum", "Hypomyelinating leucodystrophy with atrophy of basal ganglia and cerebellum", "hypomyelinating leukodystrophy with atrophy of the basal ganglia and cerebellum", "leukodystrophy, hypomyelinating, with atrophy of the basal ganglia and cerebellum", "Leukodystrophy, Hypomyelinating, With Atrophy Of The Basal Ganglia And Cerebellum", "LEUKODYSTROPHY, HYPOMYELINATING, WITH ATROPHY OF THE BASAL GANGLIA AND CEREBELLUM", "Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypomyelinating leukodystrophy 6", "shortest_name_length": 4}
{"curie": "MONDO:0030522", "names": ["SPGF64", "spermatogenic failure 64", "SPERMATOGENIC FAILURE 64"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 64", "shortest_name_length": 6}
{"curie": "UMLS:C0162386", "names": ["Subtrochanteric fracture", "subtrochanteric fracture", "subtrochanteric fractures", "Subtrochanteric Fractures", "Fractures, Subtrochanteric", "Femur fracture subtrochanteric", "femur fractures subtrochanteric", "femur fracture; subtrochanteric", "fracture; femur, subtrochanteric", "femur; fracture, subtrochanteric", "subtrochanteric; femoral fracture", "subtrochanteric fracture of femur", "Subtrochanteric fracture of femur", "fracture of neck of femur subtrochanteric", "Subtrochanteric fracture of femur (disorder)", "subtrochanteric fracture of femur (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subtrochanteric Fractures", "shortest_name_length": 24}
{"curie": "UMLS:C1404837", "names": ["Toxic Nephropathy", "drug; nephropathy", "Drug-induced Nephropathy", "Drug-Induced Nephropathy", "nephropathy; drug-induced", "Drug-Induced Kidney Injury", "Drug-Induced Renal Failure", "Drug-induced kidney injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drug-induced Nephropathy", "shortest_name_length": 17}
{"curie": "UMLS:C0855092", "names": ["B Cell Lymphoma Stage II", "Stage II B Cell Lymphoma", "Stage II B-Cell Lymphoma", "B-Cell Lymphoma Stage II", "B-cell lymphoma stage II", "Stage II B-Cell Non-Hodgkin Lymphoma", "Stage II B-Cell Non-Hodgkin's Lymphoma", "Ann Arbor Stage II B-Cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-cell lymphoma stage II", "shortest_name_length": 24}
{"curie": "UMLS:C0347703", "names": ["jugular vein injury", "Jugular vein injury", "Injury to Jugular Vein", "Injury to jugular vein", "injury of jugular vein", "Injury to jugular vein NOS", "injury of jugular vein (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jugular vein injury", "shortest_name_length": 19}
{"curie": "MONDO:0015338", "names": ["syndromic craniosynostosis", "syndrome associated with craniosynostosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic craniosynostosis", "shortest_name_length": 26}
{"curie": "MONDO:0014693", "names": ["NS10", "NOONAN SYNDROME 10", "Noonan Syndrome 10", "Noonan syndrome 10", "LZTR1 Noonan syndrome", "Noonan syndrome type 10", "Noonan syndrome caused by mutation in LZTR1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Noonan syndrome 10", "shortest_name_length": 4}
{"curie": "MONDO:0010066", "names": ["ICAS", "splenic hypoplasia", "SPLENIC HYPOPLASIA", "Asplenia, Familial", "ASPLENIA, FAMILIAL", "asplenia, familial", "Splenic hypoplasia", "Splenic Hypoplasia", "Hypoplasia of spleen", "Congenital microsplenia", "Congenital small spleen", "asplenia, isolated congenital", "ASPLENIA, ISOLATED CONGENITAL", "Congenital hypoplasia of spleen", "Hypoplasia of spleen (disorder)", "Hyposplenia, Isolated Congenital", "hyposplenia, isolated congenital", "HYPOSPLENIA, ISOLATED CONGENITAL", "Familial isolated congenital asplenia", "familial isolated congenital asplenia", "Congenital hypoplasia of spleen (disorder)", "Familial isolated congenital asplenia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial isolated congenital asplenia", "shortest_name_length": 4}
{"curie": "MONDO:0002688", "names": ["duodenum obstruction", "Obstruction duodenal", "duodenal obstruction", "Duodenal obstruction", "Duodenal Obstruction", "obstruction duodenal", "OBSTRUCTION DUODENAL", "Obstruction, Duodenal", "obstruction; duodenum", "Duodenal Obstructions", "duodenum; obstruction", "Obstructions, Duodenal", "Obstruction of duodenum", "duodenal obstruction (diagnosis)", "Obstruction of duodenum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "duodenal obstruction", "shortest_name_length": 20}
{"curie": "MONDO:0007518", "names": ["edema, familial idiopathic, prepubertal", "EDEMA, FAMILIAL IDIOPATHIC, PREPUBERTAL", "Edema, Familial Idiopathic, Prepubertal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "edema, familial idiopathic, prepubertal", "shortest_name_length": 39}
{"curie": "MONDO:0004953", "names": ["IBC NST", "ductal adenocarcinoma", "Carcinoma, Ductal, Breast", "invasive ductal carcinoma", "Invasive Ductal Carcinoma", "carcinoma infiltrating duct", "carcinoma ductal infiltrate", "Carcinoma, Infiltrating Duct", "carcinoma ductal infiltrated", "cancer breast invasive ductal", "breast cancer invasive ductal", "invasive ductal breast cancer", "Invasive ductal breast cancer", "ductal invasive breast cancer", "infiltrating ductal carcinoma", "Breast ductal cancer invasive", "Carcinomas, Infiltrating Duct", "Infiltrating Ductal Carcinoma", "ductal infiltrating carcinoma", "Invasive Ductal Carcinoma, NST", "Invasive Ductal Carcinoma, NOS", "invasive ductal carcinoma, NST", "BREAST CANCER, INVASIVE DUCTAL", "invasive ductal adenocarcinoma", "Invasive ductal carcinoma, NST", "Invasive Ductal Adenocarcinoma", "carcinomas ductal infiltrating", "Infiltrating ductular carcinoma", "invasive ductal carcinoma breast", "ductal invasive breast carcinoma", "breast invasive ductal carcinoma", "breast carcinoma ductal invasive", "Invasive ductal breast carcinoma", "Invasive Ductal Breast Carcinoma", "invasive breast ductal carcinoma", "invasive ductal breast carcinoma", "Infiltrating ductal breast cancer", "Invasive duct carcinoma of breast", "BREAST CANCER DUCTAL INFILTRATING", "Breast ductal cancer infiltrating", "Invasive Ductal Carcinoma, Breast", "Infiltrating Ductal Adenocarcinoma", "infiltrating ductal adenocarcinoma", "Carcinoma, Invasive Ductal, Breast", "Invasive ductal carcinoma of breast", "invasive ductal carcinoma of breast", "Invasive Ductal Carcinoma of Breast", "infiltrating ductal breast carcinoma", "Infiltrating Ductal Breast Carcinoma", "Infiltrating duct carcinoma of breast", "invasive ductal carcinoma of the breast", "Infiltrating ductal carcinoma of breast", "Invasive Ductal Carcinoma of the Breast", "Infiltrating Ductal Carcinoma of Breast", "infiltrating ductal carcinoma of breast", "invasive ductal carcinoma, No specific type", "Infiltrating Ductal Carcinoma of the Breast", "Invasive Ductal Carcinoma, No Specific Type", "infiltrating ductal carcinoma of the breast", "Invasive Breast Carcinoma of No Special Type", "carcinoma; infiltrating duct, unspecified site", "Infiltrating duct carcinoma of breast (disorder)", "infiltrating; ductal carcinoma, unspecified site", "carcinoma; ductal, infiltrating, unspecified site", "ductal; carcinoma, infiltrating, unspecified site", "infiltrating; ductular carcinoma, unspecified site", "carcinoma; infiltrating ductular, unspecified site", "Invasive Ductal Carcinoma, Not Otherwise Specified", "infiltrating ductal carcinoma of breast (diagnosis)", "ductular; carcinoma, infiltrating, unspecified site", "carcinoma; ductular, infiltrating, unspecified site", "infiltrating; ductal adenocarcinoma, unspecified site", "Infiltrating ductular carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "invasive ductal breast carcinoma", "shortest_name_length": 7}
{"curie": "MONDO:0012839", "names": ["IMD68", "MYD88D", "MyD88 deficiency", "MYD88 Deficiency", "MYD88 DEFICIENCY", "immunodeficiency 68", "IMMUNODEFICIENCY 68", "pyogenic bacterial infections due to MyD88 deficiency", "Recurrent Pyogenic Bacterial Infections Due To MYD88 Deficiency", "recurrent pyogenic bacterial infections due to MyD88 deficiency", "RECURRENT PYOGENIC BACTERIAL INFECTIONS DUE TO MYD88 DEFICIENCY", "PYOGENIC BACTERIAL INFECTIONS, RECURRENT, DUE TO MYD88 DEFICIENCY", "Pyogenic Bacterial Infections, Recurrent, Due To MYD88 Deficiency", "pyogenic bacterial infections, recurrent, due to MyD88 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyogenic bacterial infections due to MyD88 deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C5670656", "names": ["CNS Anaplastic Solitary Fibrous Tumor", "CNS Dedifferentiated Solitary Fibrous Tumor", "Central Nervous System Anaplastic Solitary Fibrous Tumor", "Central Nervous System Dedifferentiated Solitary Fibrous Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Dedifferentiated Solitary Fibrous Tumor", "shortest_name_length": 37}
{"curie": "UMLS:C1112424", "names": ["Post procedural urine leak"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post procedural urine leak", "shortest_name_length": 26}
{"curie": "UMLS:C0751507", "names": ["Sleep Fragmentation", "Fragmentation, Sleep"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sleep Fragmentation", "shortest_name_length": 19}
{"curie": "MONDO:0006180", "names": ["GI adenoma", "GI System Adenoma", "digestive tract adenoma", "digestive system adenoma", "Digestive System Adenoma", "gastrointestinal adenoma", "Gastrointestinal tract adenoma", "Gastrointestinal System Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "digestive system adenoma", "shortest_name_length": 10}
{"curie": "MONDO:0017235", "names": ["familial omphalocele syndrome with facial dysmorphism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial omphalocele syndrome with facial dysmorphism", "shortest_name_length": 53}
{"curie": "MONDO:0007553", "names": ["EPIDERMOLYSIS BULLOSA WITH DEFICIENCY OF GALACTOSYLHYDROXYLYSYL GLUCOSYLTRANSFERASE", "Epidermolysis Bullosa with Deficiency of Galactosylhydroxylysyl Glucosyltransferase", "epidermolysis bullosa with deficiency of galactosylhydroxylysyl glucosyltransferase"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolysis bullosa with deficiency of galactosylhydroxylysyl glucosyltransferase", "shortest_name_length": 83}
{"curie": "UMLS:C0279719", "names": ["insulin secreting adenoma", "insulin producing adenoma", "Pancreatic Beta Cell Adenoma", "Pancreatic Beta Islet Cell Adenoma", "pancreatic beta islet cell adenoma", "beta islet cell adenoma, pancreatic", "adenoma, pancreatic beta islet cell", "islet cell, beta, pancreatic adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Beta Cell Adenoma", "shortest_name_length": 25}
{"curie": "UMLS:C5670123", "names": ["Metastatic Hormone Receptor-Positive Breast Carcinoma", "Metastatic Hormone Receptor Positive Breast Carcinoma", "Metastatic Hormone Receptor Positive Breast Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Hormone Receptor-Positive Breast Carcinoma", "shortest_name_length": 53}
{"curie": "UMLS:C0685120", "names": ["Metastatic Neoplasm to the Pericardium", "secondary malignant pericardial neoplasm", "Secondary malignant neoplasm of pericardium", "Metastatic malignant neoplasm of pericardium", "Metastatic malignant neoplasm to pericardium", "malignant cardiac neoplasm pericardial secondary", "Metastatic Malignant Neoplasm in the Pericardium", "Metastatic Malignant Neoplasm to the Pericardium", "secondary malignant pericardial neoplasm (diagnosis)", "Metastatic malignant neoplasm to pericardium (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to pericardium", "shortest_name_length": 38}
{"curie": "UMLS:C5556681", "names": ["Locally Advanced Primary Malignant Brain Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Primary Malignant Brain Neoplasm", "shortest_name_length": 49}
{"curie": "MONDO:0012184", "names": ["PIERS", "PIERSON SYNDROME", "Pierson syndrome", "Pierson Syndrome", "Pierson syndrome (disorder)", "microcoria - congenital nephrosis", "microcoria-congenital nephrotic syndrome", "Microcoria-congenital nephrosis syndrome", "Microcoria-Congenital Nephrotic Syndrome", "microcoria-congenital nephrosis syndrome", "MICROCORIA-CONGENITAL NEPHROTIC SYNDROME", "microcoria - congenital nephrotic syndrome", "Microcoria and congenital nephrotic syndrome", "Microcoria and congenital nephrosis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pierson syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0521984", "names": ["Shortened therapeutic response", "Therapeutic response shortened", "Shortened therapeutic response (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Shortened therapeutic response", "shortest_name_length": 30}
{"curie": "MONDO:0002119", "names": ["COF", "Osteofibroma", "osteofibroma", "fibro osteoma", "Fibro-osteoma", "fibro-osteoma", "fibroma ossified", "Ossifying fibroma", "Ossifying Fibroma", "ossifying fibroma", "Fibroma, Ossifying", "ossifying fibromas", "Ossifying Fibromas", "Fibromas, Ossifying", "Cementifying fibroma", "Cementifying Fibroma", "Fibro-osteoma (disorder)", "Cemento-Ossifying Fibroma", "cemento-ossifying fibroma", "Cemento-ossifying fibroma", "fibroma, ossifying, benign", "juvenile ossifying fibroma", "ossifying fibroma (disease)", "peripheral ossifying fibroma", "Fibroma, Cementifying/Ossifying", "FIBROMA, CEMENTO-OSSIFYING, BENIGN", "Ossifying fibroma, calcified structure", "Cementifying fibroma, calcified structure", "Cemento-ossifying fibroma (morphologic abnormality)", "Ossifying Fibroma of the Jaws and Craniofacial Skeleton", "Ossifying fibroma, calcified structure (morphologic abnormality)", "Cementifying fibroma, calcified structure (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ossifying fibroma", "shortest_name_length": 3}
{"curie": "MONDO:0013027", "names": ["PACD", "posterior amorphous corneal dystrophy", "chromosome 12Q21.33 deletion syndrome", "POSTERIOR AMORPHOUS CORNEAL DYSTROPHY", "CHROMOSOME 12q21.33 DELETION SYNDROME", "posterior amorphous stromal dystrophy", "chromosome 12q21.33 deletion syndrome", "Posterior amorphous stromal dystrophy", "Posterior Amorphous Corneal Dystrophy", "Posterior amorphous corneal dystrophy", "corneal dystrophy, POSTERIOR amorphous", "Corneal Dystrophy, Posterior Amorphous", "CORNEAL DYSTROPHY, POSTERIOR AMORPHOUS", "Posterior amorphous corneal dystrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "posterior amorphous corneal dystrophy", "shortest_name_length": 4}
{"curie": "MONDO:0100264", "names": ["PEX10 related Zellweger spectrum disorder", "peroxisome biogenesis disorder due to PEX10 defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder due to PEX10 defect", "shortest_name_length": 41}
{"curie": "MONDO:0014310", "names": ["POIKTMP", "POIKTMP syndrome", "hereditary sclerosing poikiloderma with tendon and pulmonary involvement", "poikiloderma, hereditary sclerosing, with tendon and pulmonary involvement", "POIKILODERMA, HEREDITARY SCLEROSING, WITH TENDON AND PULMONARY INVOLVEMENT", "hereditary fibrosing poikiloderma-tendon contractures-myopathy-pulmonary fibrosis syndrome", "hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis", "POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY, AND PULMONARY FIBROSIS", "poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary sclerosing poikiloderma with tendon and pulmonary involvement", "shortest_name_length": 7}
{"curie": "MONDO:0003548", "names": ["adenosquamous breast carcinoma", "Breast Adenosquamous Carcinoma", "breast adenosquamous carcinoma", "Adenosquamous Breast Carcinoma", "adenosquamous carcinoma of breast", "metaplastic adenosquamous carcinoma", "adenosquamous carcinoma of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenosquamous breast carcinoma", "shortest_name_length": 30}
{"curie": "UMLS:C1332247", "names": ["Ampulla of Vater Intestinal-Type Adenocarcinoma", "Ampulla of Vater Invasive Intestinal Type Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ampulla of Vater Intestinal-Type Adenocarcinoma", "shortest_name_length": 47}
{"curie": "MONDO:0014278", "names": ["IMD18", "IMMUNODEFICIENCY 18", "immunodeficiency 18", "CD3epsilon deficiency", "CD3-epsilon deficiency", "CD3-EPSILON DEFICIENCY", "CD3-Epsilon deficiency", "immunodeficiency type 18", "immunodeficiency 18, SCID variant", "IMMUNODEFICIENCY 18, SCID VARIANT", "IMMUNODEFICIENCY 18, SEVERE COMBINED IMMUNODEFICIENCY VARIANT", "immunodeficiency 18, Severe combined immunodeficiency variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 18", "shortest_name_length": 5}
{"curie": "MONDO:0014442", "names": ["BBS14", "BARDET-BIEDL SYNDROME 14", "Bardet-Biedl Syndrome 14", "Bardet-Biedl syndrome 14", "Bardet-Biedl syndrome type 14", "BARDET-BIEDL SYNDROME 14 (disorder)", "Bardet-Biedl syndrome 14, modifier of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bardet-Biedl syndrome 14", "shortest_name_length": 5}
{"curie": "UMLS:C1608967", "names": ["Rhodococcus infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rhodococcus infection", "shortest_name_length": 21}
{"curie": "MONDO:0018606", "names": ["extensive peripapillary myelinated nerve fibers"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extensive peripapillary myelinated nerve fibers", "shortest_name_length": 47}
{"curie": "UMLS:C4054705", "names": ["Intermediate Soft Tissue Tumor of Uncertain Differentiation", "Intermediate Soft Tissue Neoplasm of Uncertain Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intermediate Soft Tissue Tumor of Uncertain Differentiation", "shortest_name_length": 59}
{"curie": "UMLS:C0861626", "names": ["Tongue Mucoepidermoid Carcinoma", "mucoepidermoid carcinoma of tongue", "Mucoepidermoid carcinoma of the tongue", "mucoepidermoid carcinoma of tongue (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mucoepidermoid carcinoma of the tongue", "shortest_name_length": 31}
{"curie": "UMLS:C1334218", "names": ["Cellular Rhabdomyoma", "Intermediate Rhabdomyoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intermediate Rhabdomyoma", "shortest_name_length": 20}
{"curie": "MONDO:0016010", "names": ["DiSala syndrome", "disala syndrome", "di Sala syndrome", "warfarin syndrome", "coumarin syndrome", "Coumadin syndrome", "Warfarin syndrome", "Coumarin syndrome", "heparin embryopathy", "warfarin embryopathy", "Warfarin embryopathy", "coumarin embryopathy", "dysmorphism; warfarin", "warfarin; dysmorphism", "fetal Coumadin syndrome", "Fetal Coumadin Syndrome", "fetal warfarin syndrome", "Fetal Warfarin Syndrome", "Fetal warfarin syndrome", "Foetal warfarin syndrome", "Warfarin embryofetopathy", "warfarin embryofetopathy", "Dysmorphism due to warfarin", "congenital warfarin syndrome", "Congenital warfarin syndrome", "Fetal anticoagulant syndrome", "fetal anticoagulant syndrome", "vitamin K-antagonist embryopathy", "Vitamin K antagonist embryopathy", "vitamin K antagonist embryopathy", "Fetal warfarin syndrome (disorder)", "vitamin K-antagonist embryofetopathy", "vitamin K antagonist embryofetopathy", "Vitamin K antagonist embryofetopathy", "vitamin K antagonists embryofetopathy", "embryofetopathy due to oral anticoagulant therapy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vitamin K-antagonist embryofetopathy", "shortest_name_length": 15}
{"curie": "UMLS:C1520068", "names": ["Vulvar Acquired Melanocytic Nevus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Acquired Melanocytic Nevus", "shortest_name_length": 33}
{"curie": "UMLS:C0746921", "names": ["Nodal Mass", "NODAL MASS", "nodal mass", "Lymph Node Mass"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymph Node Mass", "shortest_name_length": 10}
{"curie": "UMLS:C1275280", "names": ["Superficial Angiomyxoma", "Superficial angiomyxoma", "Superficial angiomyxoma (disorder)", "Superficial angiomyxoma (diagnosis)", "neoplasm of uncertain behavior angiomyxoma superficial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Superficial angiomyxoma", "shortest_name_length": 23}
{"curie": "MONDO:0000470", "names": ["Endocardiopathy", "endocardiopathy", "endocardial disease", "endocardium disease", "Endocardial disease", "endocardium disorder", "disease of endocardium", "disorder of endocardium", "Endocardial disease NOS", "Disorder of endocardium", "diseases of endocardium", "endocardium disease or disorder", "disease or disorder of endocardium", "Disorder of endocardium (disorder)", "diseases of endocardium (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endocardium disorder", "shortest_name_length": 15}
{"curie": "MONDO:0008168", "names": ["fibroma ovary", "OVARY, FIBROMA", "Ovarian fibroma", "ovarian fibroma", "Ovarian Fibroma", "Fibroma of Ovary", "fibroma of ovary", "Fibroma of ovary", "Ovarian fibromata", "OVARIAN FIBROMATA", "ovarian fibromata", "Ovarian Fibromata", "Fibroma of the Ovary", "fibroma of the ovary", "ovarian fibroma (disease)", "Fibroma of ovary (disorder)", "fibroma of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian fibroma", "shortest_name_length": 13}
{"curie": "MONDO:0021060", "names": ["rasopathy", "RASopathy", "Ras protein signal transduction disease", "disorder of Ras protein signal transduction", "RAS/mitogen-activated protein kinase syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "RASopathy", "shortest_name_length": 9}
{"curie": "UMLS:C0854372", "names": ["mastication; problem", "problem; mastication", "Mastication disorder", "disorder; mastication", "mastication; disorder", "Disturbance of mastication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mastication disorder", "shortest_name_length": 20}
{"curie": "UMLS:C0156263", "names": ["ureter; fistula", "fistula; ureter", "Ureteral fistula", "ureteral fistula", "Ureteric Fistula", "Ureteric fistula", "fistulas ureteral", "Ureteric fistula (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ureteric fistula", "shortest_name_length": 15}
{"curie": "MONDO:0017071", "names": ["thoracolumbosacral spina bifida cystica"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thoracolumbosacral spina bifida cystica", "shortest_name_length": 39}
{"curie": "MONDO:0001778", "names": ["skin Dermoid", "skin dermoid", "Skin Dermoid", "skin dermoid cyst", "Skin Dermoid Cyst", "Dermoid cyst of skin", "Cystic Skin Teratoma", "Dermoid Cyst of Skin", "cystic skin teratoma", "dermoid cyst of skin", "Cutaneous Dermoid Cyst", "cutaneous dermoid cyst", "dermoid cyst of the skin", "Dermoid Cyst of the Skin", "Subcutaneous Dermoid Cyst", "zone of skin dermoid cyst", "subcutaneous dermoid cyst", "dermoid cyst of skin (finding)", "Dermoid cyst of skin (disorder)", "dermoid cyst of skin (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermoid cyst of skin", "shortest_name_length": 12}
{"curie": "MONDO:0016107", "names": ["Steinert", "steinert disease", "STEINERT DISEASE", "Steinert disease", "myotonic disease", "Steinert Disease", "syndrome steinert", "Steinerts Disease", "steinert syndrome", "disease steinerts", "Disease, Steinert", "Steinert syndrome", "steinert's disease", "Myotonia atrophica", "MYOTONIA ATROPHICA", "dystrophy myotonic", "Steinert's Disease", "Steinert's disease", "myotonia atrophica", "myotonic dystrophy", "Myotonic dystrophy", "Myotonic Dystrophy", "Myotonia Atrophica", "Disease, Steinert's", "myotonia; atrophica", "dystrophy; myotonic", "Dystrophy, Myotonic", "Atrophica, Myotonia", "atrophica; myotonia", "myotonic; dystrophy", "DYSTROPHY, MYOTONIC", "Myotonia Atrophicas", "Atrophicas, Myotonia", "Myotonic Dystrophy 1", "myotonia dystrophica", "Myotonia dystrophica", "Myotonia Dystrophica", "dystrophia myotonica", "Myotonic Dystrophies", "Dystrophia myotonica", "Dystrophia Myotonica", "Myotrophia dystonica", "Dystrophica, Myotonia", "myotonia; dystrophica", "Dystrophies, Myotonic", "Myotonia Dystrophicas", "dystrophica; myotonia", "Myotonica, Dystrophia", "Dystrophia Myotonicas", "Dystrophicas, Myotonia", "Myotonicas, Dystrophia", "Dystrophia Myotonica 1", "DM - Dystrophia myotonica", "DM - dystrophia myotonica", "Myotonic muscular dystrophy", "muscular dystrophy myotonic", "dystrophy muscular myotonic", "Steinert Myotonic Dystrophy", "MYOTONIC MUSCULAR DYSTROPHY", "MUSCULAR DYSTROPHY MYOTONIC", "myotonic muscular dystrophy", "Dystrophy, Steinert Myotonic", "inherited myotonic dystrophy", "Myotonic Dystrophy, Steinert", "Myotonic dystrophy (disorder)", "dystrophy; muscular, myotonic", "muscular; dystrophy, myotonic", "Dystrophia myotonica [Steinert]", "CURSCHMANN-BATTEN-STEINERT SYNDROME", "Steinert myotonic dystrophy syndrome", "myotonic muscular dystrophy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myotonic dystrophy", "shortest_name_length": 8}
{"curie": "MONDO:0010946", "names": ["CMH6", "hypertrophic cardiomyopathy 6", "cardiomyopathy, hypertrophic 6", "hypertrophic cardiomyopathy type 6", "PRKAG2 hypertrophic cardiomyopathy", "cardiomyopathy, familial hypertrophic 6", "CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6", "cardiomyopathy, familial hypertrophic, 6", "Cardiomyopathy, Familial Hypertrophic, 6", "Familial Hypertrophic Cardiomyopathy Type 6", "cardiomyopathy, familial hypertrophic, type 6", "CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6 (disorder)", "hypertrophic cardiomyopathy caused by mutation in PRKAG2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophic cardiomyopathy 6", "shortest_name_length": 4}
{"curie": "UMLS:C4086174", "names": ["Childhood Testicular Mature Teratoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Testicular Mature Teratoma", "shortest_name_length": 36}
{"curie": "MONDO:0015167", "names": ["ABS", "Adam Complex", "Pseudoainhum", "ADAM COMPLEX", "Amniotic Band", "amniotic band", "AMNIOTIC BAND", "Adam syndrome", "Amniotic band", "Pseudo-ainhum", "amniotic bands", "Amniotic bands", "Band, Amniotic", "Amniotic Bands", "Bands, Amniotic", "Streeter anomaly", "STREETER ANOMALY", "amniotic banding", "Streeter Syndrome", "Amniotic adhesion", "Streeter dysplasia", "Syndrome, Streeter", "Amniotic stricture", "Congenital amputation", "amputation, congenital", "AMNIOTIC BAND SYNDROME", "Amniotic band syndrome", "amniotic band sequence", "Amniotic Band Syndrome", "AMPUTATION, CONGENITAL", "Amniotic band sequence", "amniotic band syndrome", "AMNIOTIC BAND SEQUENCE", "Amniotic Band Sequence", "Amniotic band anomalad", "Amputation, Congenital", "Amniotic bands sequence", "familial amniotic bands", "amniotic bands sequence", "Syndrome, Amniotic Band", "Familial amniotic bands", "Pseudo-ainhum (disorder)", "Amniotic constriction ring", "constriction band syndrome", "Amniotic Band Constriction", "Constriction ring syndrome", "amniotic band constriction", "Amniotic constriction band", "Constriction band syndrome", "amniotic constriction band", "Constriction rings syndrome", "constriction rings syndrome", "amniotic bands constriction", "Amniotic adhesion (disorder)", "Congenital constriction band", "congenital ring constrictions", "Congenital ring constrictions", "Congenital constricting bands", "congenital constricting bands", "CONSTRICTING bands, congenital", "Deformity due to Amniotic Band", "deformity due to amniotic band", "Constricting Bands, Congenital", "CONSTRICTING BANDS, CONGENITAL", "Deformity due to amniotic band", "terminal transverse defects of arm", "amniotic band syndrome (diagnosis)", "Congenital constriction band sequence", "Constriction ring syndrome (disorder)", "Pseudoainhum (morphologic abnormality)", "amniotic deformity-adhesion-mutilation syndrome", "Constriction band abnormality of placental amnion", "constriction band abnormality of placental amnion", "constriction band abnormality of placental amnion (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amniotic band syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0001402", "names": ["cancer vagina", "vagina cancer", "Vagina Cancer", "vaginal tumor", "cancer vaginal", "Cancer, Vagina", "Vagina--Cancer", "Vaginal Cancer", "Vagina Cancers", "VAGINAL CANCER", "vaginal cancer", "Vaginal cancer", "Vaginal Cancers", "vagina neoplasm", "Cancers, Vagina", "Cancer, Vaginal", "vaginal cancers", "Cancer of Vagina", "Cancer of vagina", "cancer of vagina", "Cancers, Vaginal", "Vaginal Neoplasms", "Vaginal cancer NOS", "neoplasm of vagina", "cancer of the vagina", "Cancer of the Vagina", "Malignant Vagina Tumor", "malignant vagina tumor", "Malignant Vaginal Tumor", "malignant vaginal tumor", "Malignant Vagina Neoplasm", "Malignant Tumor of Vagina", "malignant vagina neoplasm", "Malignant tumor of vagina", "malignant tumor of vagina", "Malignant Vaginal Neoplasm", "malignant vaginal neoplasm", "Malignant tumour of vagina", "VAGINAL NEOPLASM MALIGNANT", "Vaginal neoplasm malignant", "Vaginal neoplasms malignant", "Malignant neoplasm of vagina", "Malignant Neoplasm of Vagina", "malignant neoplasm of vagina", "malignant tumor of the vagina", "Malignant Tumor of the Vagina", "Malignant Neoplasm of the Vagina", "malignant neoplasm of the vagina", "Malignant neoplasm of vagina, NOS", "Malignant tumor of vagina (disorder)", "malignant neoplasm of vagina (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vaginal cancer", "shortest_name_length": 13}
{"curie": "UMLS:C1698626", "names": ["Small intestinal mucositis", "Small Intestinal Mucositis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Intestinal Mucositis", "shortest_name_length": 26}
{"curie": "UMLS:C0677745", "names": ["Mantle Cell Lymphoma Stage II", "Stage II Mantle Cell Lymphoma", "Mantle cell lymphoma stage II", "stage II mantle cell lymphoma", "lymphoma, stage II mantle cell lymphoma", "Ann Arbor Stage II Mantle Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage II Mantle Cell Lymphoma", "shortest_name_length": 29}
{"curie": "UMLS:C4054384", "names": ["Human Immunodeficiency Virus Associated Nephrotic Syndrome", "Nephrotic Syndrome - Human Immunodeficiency Virus Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - Human Immunodeficiency Virus Associated", "shortest_name_length": 58}
{"curie": "MONDO:0016033", "names": ["CDL", "BDLS", "CDLS", "De Lange", "Bruck-de Lange", "Amsterdam type", "Amsterdam dwarf", "Dwarf, Amsterdam", "de Lange syndrome", "DE LANGE SYNDROME", "De Lange Syndrome", "Cornelia de Lange", "de lange syndrome", "De Lange syndrome", "De Lange's Syndrome", "De Lange's syndrome", "typus amstelodamensis", "Bruck-de Lange syndrome", "Cornelia de Lange syndrome", "syndrome cornelia de lange", "lange syndrome cornelia de", "cornelia de lange syndrome", "Cornelia De Lange Syndrome", "BRACHMANN-DE LANGE SYNDROME", "Brachmann-De Lange Syndrome", "cornelia de langes syndrome", "brachmann de lange syndrome", "Brachmann De Lange Syndrome", "Brachmann de Lange syndrome", "Brachmann-de Lange syndrome", "Cornelia de Lange's syndrome", "De Lange syndrome (disorder)", "cornelia de lange's syndrome", "Syndrome, Brachmann-De Lange", "Degenerative amsterodamensis typus", "Degenerative amstelodamensis typus", "Typus Degenerativus Amstelodamensis", "Typus degenerativus amstelodamensis", "TYPUS DEGENERATIVUS AMSTELODAMENSIS", "Brachmann-Cornelia de Lange syndrome", "status degenerativus amstelodamensis", "Amstelodamensis, Typus Degenerativus", "Cornelia de Lange syndrome (diagnosis)", "Brachmann-Cornelia de Lange (BCDL) syndrome (BDLS)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cornelia de Lange syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C2698751", "names": ["Pediatric nodal marginal zone lymphoma", "Childhood Nodal Marginal Zone Lymphoma", "Pediatric Nodal Marginal Zone Lymphoma", "Paediatric nodal marginal zone lymphoma", "Pediatric nodal marginal zone lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pediatric nodal marginal zone lymphoma", "shortest_name_length": 38}
{"curie": "MONDO:0100126", "names": ["P5CS deficiency", "delta1-pyrroline-5-carboxylate synthetase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "P5CS deficiency", "shortest_name_length": 15}
{"curie": "MONDO:0012008", "names": ["Lelis Syndrome", "Lelis syndrome", "LELIS SYNDROME", "ectodermal dysplasia-acanthosis nigricans syndrome", "Ectodermal dysplasia-acanthosis nigricans syndrome", "Ectodermal dysplasia with acanthosis nigricans syndrome", "ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH ACANTHOSIS NIGRICANS", "Ectodermal Dysplasia, Hypohidrotic, with Acanthosis Nigricans", "ectodermal dysplasia, hypohidrotic, with acanthosis nigricans", "Ectodermal dysplasia with acanthosis nigricans syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lelis syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C1332918", "names": ["Cervical Microglandular Polyp", "Microglandular Polyp of Cervix", "Microglandular Polyp of the Cervix", "Uterine Cervix Microglandular Polyp", "Microglandular Polyp of Uterine Cervix", "Microglandular Polyp of the Uterine Cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Microglandular Polyp", "shortest_name_length": 29}
{"curie": "MONDO:0003137", "names": ["Glomerulonephritis diffuse", "diffuse glomerulonephritis", "Diffuse Glomerulonephritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diffuse glomerulonephritis", "shortest_name_length": 26}
{"curie": "MONDO:0008492", "names": ["SSKS", "stiff skin syndrome", "Stiff skin syndrome", "Stiff Skin Syndrome", "STIFF SKIN SYNDROME", "STIFF skin syndrome", "Stiff skin syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stiff skin syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C5420266", "names": ["Refractory Primitive Neuroectodermal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Primitive Neuroectodermal Tumor", "shortest_name_length": 42}
{"curie": "UMLS:C0281869", "names": ["Hodgkin disease in remission", "Hodgkin Lymphoma in Remission", "Hodgkin lymphoma in remission", "Hodgkin's Disease in Remission", "Hodgkin's disease in remission", "Hodgkin's lymphoma in remission", "Hodgkin's disease in remission (disorder)", "Hodgkin lymphoma in remission (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's disease in remission", "shortest_name_length": 28}
{"curie": "MONDO:0007534", "names": ["WBS", "BWS", "BWCR", "emg syndrome", "syndrome emg", "EMG Syndrome", "EMG SYNDROME", "EMG syndrome", "Syndrome, EMG", "EMG Syndromes", "beckwith syndrome", "Beckwith syndrome", "Wiedemann syndrome", "syndrome wiedemann", "wiedemann syndrome", "Wiedemann Syndrome", "Beckwith-Wiedemann", "Beckwith's syndrome", "beckwith's syndrome", "Syndrome, Wiedemann", "Wiedemann Syndromes", "Beckwith Wiedemann Syndrome", "beckwith wiedemann syndrome", "wiedemann beckwith syndrome", "WIEDEMANN-BECKWITH SYNDROME", "Wiedemann Beckwith Syndrome", "Beckwith-Wiedemann syndrome", "beckwith syndrome wiedemann", "Wiedemann-Beckwith syndrome", "beckwith-wiedemann syndrome", "Beckwith-Wiedemann Syndrome", "BECKWITH-WIEDEMANN SYNDROME", "Wiedemann-Beckwith Syndrome", "Syndrome, Beckwith-Wiedemann", "Syndrome, Wiedemann-Beckwith", "Beckwith syndrome (diagnosis)", "Wiedemann-Beckwith syndrome (WBS)", "Wiedemann-Beckwith-Combs syndrome", "Wiedemann Beckwith Syndrome (WBS)", "macroglossia-omphalocele syndrome", "Wiedemann-Beckwith Syndrome (WBS)", "Wiedemann-Beckwith Syndromes (WBS)", "Syndrome, Wiedemann-Beckwith (WBS)", "Beckwith-Wiedemann syndrome (BW, BWS)", "Beckwith-Wiedemann syndrome (disorder)", "EXOMPHALOS-MACROGLOSSIA-GIGANTISM SYNDROME", "Exomphalos-macroglossia-gigantism syndrome", "exomphalos macroglossia gigantism syndrome", "Exomphalos Macroglossia Gigantism Syndrome", "Exomphalos-Macroglossia-Gigantism Syndrome", "familial macroglossia-omphalocele syndrome", "exomphalos-macroglossia-gigantism syndrome", "Exomphalos-Macroglossia-Gigantism Syndromes", "Syndrome, Exomphalos-Macroglossia-Gigantism", "BECKWITH-WIEDEMANN SYNDROME CHROMOSOME REGION", "Beckwith-Wiedemann syndrome chromosome region", "macroglossia-omphalocele-visceromegaly syndrome", "exomphalos-macroglossia-gigantism (EMG) syndrome", "Beckwith-Wiedemann Syndrome/Isolated Hemihyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Beckwith-Wiedemann syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C4744429", "names": ["Locally Advanced Unresectable Gastric Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Unresectable Gastric Adenocarcinoma", "shortest_name_length": 52}
{"curie": "MONDO:0014942", "names": ["DEE45", "EIEE45", "early infantile epileptic encephalopathy 45", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 45", "developmental and epileptic encephalopathy 45", "epileptic encephalopathy, early infantile, 45", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 45", "developmental and epileptic encephalopathy, 45", "GABRB1 early infantile epileptic encephalopathy", "epileptic encephalopathy, early infantile, type 45", "epileptic encephalopathy, early infantile, 45; EIEE45", "early infantile epileptic encephalopathy caused by mutation in GABRB1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 45", "shortest_name_length": 5}
{"curie": "MONDO:0012397", "names": ["brachydactyly, coloboma, and anterior segment dysgenesis", "Brachydactyly, Coloboma, And Anterior Segment Dysgenesis", "BRACHYDACTYLY, COLOBOMA, AND ANTERIOR SEGMENT DYSGENESIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly, coloboma, and anterior segment dysgenesis", "shortest_name_length": 56}
{"curie": "UMLS:C0460048", "names": ["bowel large obstruction", "large bowel obstruction", "Large bowel obstruction", "LARGE BOWEL OBSTRUCTION", "Large intestinal obstruction", "obstruction large intestinal", "Large intestinal obstruction NOS", "Large bowel obstruction (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Large bowel obstruction", "shortest_name_length": 23}
{"curie": "UMLS:C0032087", "names": ["Poisoning;plant", "Plant poisoning", "Plant Poisoning", "plant poisoning", "plant poisonings", "Poisoning, Plant", "Plant Poisonings", "poisoning plants", "poisoning; plants", "plants; poisoning", "Poisonings, Plant", "poisoning by plants", "poisoning by plants (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Plant Poisoning", "shortest_name_length": 15}
{"curie": "UMLS:C0750907", "names": ["Amnestic State", "Amnestic States", "State, Amnestic", "States, Amnestic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Amnestic State", "shortest_name_length": 14}
{"curie": "UMLS:C0040715", "names": ["Translocation", "Translocations", "Genetic Translocation", "genetic translocation", "Translocation, Genetic", "genetic translocations", "Genetic Translocations", "Translocations, Genetic", "CHROMOSOME TRANSLOCATION", "Chromosome Translocation", "chromosome translocation", "Translocation (Genetics)", "Chromosomal Translocation", "chromosome; translocation", "chromosomes translocation", "chromosomal translocation", "chromosome translocations", "Chromosomal translocation", "translocation; chromosomes", "CHROMOSOMAL TRANSLOCATIONS", "Translocation (Chromosome)", "chromosomal translocations", "Chromosomal Translocations", "Translocation, Chromosomal", "Translocations, Chromosomal", "Chromosomal translocation, NOS", "Chromosomal Translocation Process", "Chromosomal translocation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chromosomal translocation", "shortest_name_length": 13}
{"curie": "MONDO:0023240", "names": ["gigantism advanced bone age hoarse cry"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gigantism advanced bone age hoarse cry", "shortest_name_length": 38}
{"curie": "MONDO:0043185", "names": ["Pointer syndrome", "pointer syndrome", "skeletal abnormalities, camptodactyly, facial anomalies, and feeding difficulties", "Skeletal abnormalities, camptodactyly, facial anomalies, and feeding difficulties"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pointer syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0014059", "names": ["MCOPS15", "MCOPCB9", "MICROPHTHALMIA, SYNDROMIC 15", "microphthalmia, syndromic 15", "MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 9", "microphthalmia, isolated, with coloboma 9", "TENM3 microphthalmia, isolated, with coloboma", "microphthalmia, isolated, with coloboma type 9", "MICROPHTHALMIA AND/OR COLOBOMA WITH DEVELOPMENTAL DELAY", "microphthalmia, isolated, with coloboma caused by mutation in TENM3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microphthalmia, isolated, with coloboma 9", "shortest_name_length": 7}
{"curie": "MONDO:0021506", "names": ["benign spinal cord tumor", "Benign Spinal Cord Tumor", "Benign Tumor of Spinal Cord", "Benign tumor of spinal cord", "Benign Spinal Cord Neoplasm", "spinal cord benign neoplasm", "benign spinal cord neoplasm", "Neoplasm benign;spinal cord", "benign tumor of spinal cord", "Benign tumour of spinal cord", "spinal cord neoplasm, benign", "Spinal Cord Neoplasm, Benign", "Spinal Cord Neoplasms, Benign", "benign neoplasm of spinal cord", "Benign neoplasm of spinal cord", "Benign Neoplasm of Spinal Cord", "Benign Tumor of the Spinal Cord", "benign tumor of the spinal cord", "Benign spinal cord neoplasm NOS", "Spinal cord neoplasm benign NOS", "Benign Neoplasm of the Spinal Cord", "benign neoplasm of the spinal cord", "benign spinal cord tumor (diagnosis)", "Benign neoplasm of spinal cord (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of spinal cord", "shortest_name_length": 24}
{"curie": "MONDO:0011968", "names": ["DMDA2", "LGMDR3", "LGMD2D", "LGMD type 2D", "Adhalinopathies", "Primary Adhalinopathy", "primary adhalinopathy", "Adhalinopathy, primary", "ADHALINOPATHY, PRIMARY", "Adhalinopathy, Primary", "Alpha-Sarcoglycanopathy", "Alpha-sarcoglycanopathy", "Alpha sarcoglycanopathy", "Primary Adhalinopathies", "Alpha Sarcoglycanopathy", "Adhalinopathies, Primary", "Alpha-Sarcoglycanopathies", "Alpha Sarcoglycanopathies", "Alpha-sarcoglycan-related LGMD R3", "Limb-Girdle Muscular Dystrophy Type 2D", "Limb-girdle muscular dystrophy type 2D", "limb-girdle muscular dystrophy type 2D", "Limb girdle muscular dystrophy type 2D", "Limb-Girdle Muscular Dystrophy, Type 2D", "Limb Girdle Muscular Dystrophy, Type 2D", "limb-girdle muscular dystrophy, type 2D", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2D", "Muscular Dystrophy, Limb-Girdle, Type 2D", "LGMD due to alpha-sarcoglycan deficiency", "muscular dystrophy, limb-girdle, type 2D", "muscular dystrophy limb-girdle with alpha-sarcoglycan", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 3", "muscular dystrophy, limb-girdle, autosomal recessive 3", "SGCA autosomal recessive limb-girdle muscular dystrophy", "Autosomal recessive limb-girdle muscular dystrophy type 2D", "Autosomal recessive limb girdle muscular dystrophy type 2D", "autosomal recessive limb-girdle muscular dystrophy type 2D", "Alpha-sarcoglycan-related limb-girdle muscular dystrophy R3", "Duchenne-like autosomal recessive muscular dystrophy type 2", "Duchenne-Like Autosomal Recessive Muscular Dystrophy, Type 2", "Duchenne-like autosomal recessive muscular dystrophy, type 2", "DUCHENNE-LIKE AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, TYPE 2", "Duchenne Like Autosomal Recessive Muscular Dystrophy, Type 2", "Muscular Dystrophy Limb Girdle with Alpha Sarcoglycan Deficiency", "Muscular Dystrophy Limb-Girdle with Alpha-Sarcoglycan Deficiency", "limb-girdle muscular dystrophy due to alpha-sarcoglycan deficiency", "Limb-girdle muscular dystrophy due to alpha-sarcoglycan deficiency", "Autosomal recessive limb girdle muscular dystrophy type 2D (disorder)", "Alpha-sarcoglycanopathy LGMD2D (limb girdle muscular dystrophy type 2D)", "autosomal recessive limb-girdle muscular dystrophy caused by mutation in SGCA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive limb-girdle muscular dystrophy type 2D", "shortest_name_length": 5}
{"curie": "MONDO:0006802", "names": ["SIADH", "siadh", "siadhs", "ADH inappropriate", "inappropriate adh", "Inappropriate ADH", "ADH INAPPROPRIATE", "INAPPROPRIATE ADH", "ectopic ADH secretion", "Ectopic ADH Secretion", "SCHWARTZ-BARTTER SYNDROME", "Schwartz Bartter Syndrome", "Schwartz-Bartter syndrome", "Schwartz-Bartter Syndrome", "inappropriate ADH syndrome", "Inappropriate ADH Syndrome", "Syndrome inappropriate ADH", "adh inappropriate syndrome", "Inappropriate ADH syndrome", "Syndrome, Schwartz-Bartter", "SYNDROME INAPPROPRIATE ADH", "adh inappropriate syndromes", "Inappropriate ADH secretion", "inappropriate adh secretion", "Inappropriate ADH Secretion", "ADH Syndrome, Inappropriate", "adh inappropriate secretion", "ADH INAPPROPRIATE SECRETION", "ADH inappropriate secretion", "Syndrome, Inappropriate ADH", "inappropriate ADH secretion", "SYNDROME OF INAPP ADH SECRETION", "inappropriate ADH syndrome (SIADH)", "Inappropriate vasopressin secretion", "antidiuretic; hormone syndrome (SIADH)", "ectopic antidiuretic hormone secretion", "Syndrome of inappropriate antidiuresis", "Ectopic Antidiuretic Hormone Secretion", "Syndrome of inappropriate ADH production", "syndrome of inappropriate secretion of ADH", "Syndrome of inappropriate secretion of ADH", "inappropriate Arginine vasopressin secretion", "Inappropriate anti-diuretic hormone syndrome", "Inappropriate Vasopressin Secretion Syndrome", "Inappropriate Arginine Vasopressin Secretion", "Inappropriate antidiuretic hormone secretion", "SYNDROME INAPPROPRIATE ANTI DIURETIC HORMONE", "Antidiuretic Hormone, Inappropriate Secretion", "SIAD - Syndrome of inappropriate antidiuresis", "Syndrome of Inappropriate Antidiuretic Hormone", "SYNDROME OF INAPPROPRIATE ANTIDIURETIC HORMONE", "syndrome of inappropriate antidiuretic hormone", "Syndrome of Inappropriate Vasopressin Secretion", "Syndrome of inappropriate vasopressin secretion", "syndrome of inappropriate vasopressin secretion", "INAPPROPRIATE SECRETION OF ANTIDIURETIC HORMONE", "Syndrome of Inappropriate ADH (SIADH) Secretion", "inadequate; secretion antidiuretic hormone (syndrome)", "inappropriate antidiuretic hormone secretion syndrome", "Inappropriate Antidiuretic Hormone Secretion Syndrome", "Syndrome of inappropriate antidiuretic hormone (SIADH)", "antidiuretic; hormone, inappropriate secretion (SIADH)", "SIADH (syndrome of inappropriate antidiuretic hormone)", "hormone secretion; antidiuretic, inadequate (syndrome)", "syndrome of Inappropriate Antidiuretic Hormone Secretion", "Syndrome of Inappropriate Antidiuretic Hormone Secretion", "syndrome of inappropriate antidiuretic hormone secretion", "Syndrome of inappropriate antidiuretic hormone secretion", "inappropriate secretion of antidiuretic hormone; syndrome", "syndrome; inappropriate secretion of antidiuretic hormone", "hormone; secretion, antidiuretic, inappropriate (syndrome)", "secretion; hormone, antidiuretic, inappropriate (syndrome)", "Syndrome of inappropriate vasopressin secretion (disorder)", "syndrome of inappropriate secretion of antidiuretic hormone", "ANTIDIURETIC HORMONE INAPPROPRIATE SECRETION SYNDROME SIADH", "Syndrome of inappropriate secretion of antidiuretic hormone", "ANTIDIURETIC HORMONE INAPPROPRIATE SECRETION SYNDROME <SIADH>", "SIADH - Syndrome of inappropriate secretion of antidiuretic hormone", "SIADH; (syndrome of inappropriate secretion of antidiuretic hormone)", "syndrome of inappropriate secretion of antidiuretic hormone (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inappropriate ADH syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0001099", "names": ["Lactocele", "lactocele", "milk cyst", "Milk cyst", "cysts milk", "milk; cyst", "cyst; milk", "Galactocele", "galactocele", "Galactocoele", "Lacteal cyst", "galactoceles", "lacteal cyst", "Lactocele (disorder)", "galactocele (diagnosis)", "Galactocoele of childhood", "lactation disorder galactocele", "galactocele due to lactation disorder", "galactocele due to lactation disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lactocele", "shortest_name_length": 9}
{"curie": "UMLS:C0349761", "names": ["AV Graft Aneurysm", "Arteriovenous Graft Aneurysm", "Arteriovenous graft aneurysm", "Arteriovenous graft aneurysm (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arteriovenous graft aneurysm", "shortest_name_length": 17}
{"curie": "UMLS:C5237419", "names": ["Refractory Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Neuroendocrine Carcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C0442886", "names": ["Secondary Infection", "Secondary infection", "secondary infection", "Secondary Infections", "infections secondary", "Infection, Secondary", "Infections, Secondary", "Secondary infection NOS", "Secondary infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary Infections", "shortest_name_length": 19}
{"curie": "MONDO:0012342", "names": ["dup(7)(q11.23)", "Dup(7)(q11.23)", "trisomy 7q11.23", "Trisomy 7q11.23", "WBS Duplication Syndrome", "Wbs Duplication Syndrome", "Wbs Duplication syndrome", "WBS DUPLICATION SYNDROME", "WBS TRIPLICATION SYNDROME", "Wbs triplication syndrome", "7q11.23 duplication syndrome", "SOMERVILLE-VAN DER AA SYNDROME", "Somerville-Van Der AA Syndrome", "Somerville-Van Der Aa syndrome", "7q11.23 microduplication syndrome", "Chromosome 7q11.23 Duplication Syndrome", "chromosome 7q11.23 duplication syndrome", "CHROMOSOME 7q11.23 DUPLICATION SYNDROME", "chromosome 7Q11.23 Duplication syndrome", "chromosome 7Q11.23 triplication syndrome", "CHROMOSOME 7q11.23 TRIPLICATION SYNDROME", "William-Beuren region duplication syndrome", "Williams-Beuren Region Duplication Syndrome", "WILLIAMS-BEUREN REGION DUPLICATION SYNDROME", "Williams-Beuren region DUPLICATION syndrome", "7q11.23 microduplication syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "7q11.23 microduplication syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0001397", "names": ["mononeuropathy", "Mononeuropathy", "Mononeuropathies", "mononeuropathies", "Mononeuropathy NOS", "Single damaged nerve", "Mononeuropathy (disorder)", "mononeuropathy (diagnosis)", "Mononeuropathy, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mononeuropathy", "shortest_name_length": 14}
{"curie": "MONDO:0021088", "names": ["Papillary meningioma", "papillary meningioma", "Papillary Meningioma", "Papillary Meningiomas", "Meningioma, Papillary", "Meningiomas, Papillary", "papillary meningioma (diagnosis)", "Papillary meningioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papillary meningioma", "shortest_name_length": 20}
{"curie": "MONDO:0017858", "names": ["M6", "AEL", "AML M6", "aml m6", "AML-M6", "FAB M6", "Fab M6", "AML M6 type", "Di Guglielmo", "Erythroleukemia", "ERYTHROLEUKEMIA", "erythroleukemia", "ERYTHROLEUKEMIAS", "Erythroleukaemia", "Erythroleukemias", "erythroleukaemia", "[M]Erythroleukemia", "DIGUGLIELMO DISEASE", "Erythremic myelosis", "Guglielmo's disease", "Erythremic Myeloses", "Erythremic Myelosis", "erythremic myelosis", "Myelosis erythremic", "DiGugliemo syndrome", "[M]Erythroleukaemia", "MYELOSIS ERYTHREMIC", "ERYTHREMIC MYELOSIS", "di guglielmo disease", "Myelosis erythraemic", "Erythraemic myelosis", "Di Guglielmo Disease", "Myeloses, Erythremic", "erythremic; myelosis", "myelosis; erythremic", "Myelosis, Erythremic", "ERYTHRAEMIC MYELOSIS", "Di Guglielmos Disease", "DI GUGLIELMO SYNDROME", "Di Guglielmo Syndrome", "acute erythroleukemia", "Di Guglielmo syndrome", "Disease, Di Guglielmo", "Di Guglielmo's Disease", "di Guglielmo's disease", "SYNDROME DIGUGLIELMO'S", "Di Guglielmo's disease", "Syndrome DiGuglielmo's", "diguglielmo's syndrome", "erythroblastic leukemia", "Erythroblastic Leukemia", "Di Guglielmo's syndrome", "Erythroleukemia, FAB M6", "Disease, Di Guglielmo's", "DI GUGLIELMO'S SYNDROME", "acute erythroid leukemia", "Acute erythroid leukemia", "erythroid leukemia acute", "Acute Erythroid Leukemia", "Erythroleukaemia, FAB M6", "Erythremic myelosis, NOS", "Acute myeloid leukemia M6", "Acute erythremic myelosis", "acute myeloid leukemia M6", "M6 acute myeloid leukemia", "M6 Acute Myeloid Leukemia", "Acute erythroid leukaemia", "M6 - Acute erythroleukemia", "myelosis; erythremic, acute", "M6 - Acute erythroleukaemia", "Myeloid Leukemia, Acute, M6", "erythremic; myelosis, acute", "erythroleukemia (diagnosis)", "Acute erythroid leukemia NOS", "Leukemia, Myeloid, Acute, M6", "acute erythroblastic leukemia", "acute myeloid leukemia FAB-M6", "Acute Erythroblastic Leukemia", "M6 OR Acute Erythroid Leukemia", "Acute Erythroblastic Leukemias", "LEUKEMIA, ERYTHROID, MALIGNANT", "Erythroblastic Leukemia, Acute", "leukemia, erythroid, malignant", "Leukemia, Acute Erythroblastic", "Erythroblastic Leukemias, Acute", "Acute myeloid leukemia, M6 type", "Leukemias, Acute Erythroblastic", "Leukemia, Erythroblastic, Acute", "Acute myeloid leukaemia, M6 type", "acute erythroleukemia M6b subtype", "acute erythroleukemia M6a subtype", "M6 type acute myelogenous leukemia", "acute myelogenous leukemia M6 type", "Erythroleukemia, FAB M6 (disorder)", "AML (acute myeloid leukemia), M6 type", "AML (acute myeloid leukaemia), M6 type", "Erythroleukemia without mention of remission", "Erythroleukaemia without mention of remission", "M6 type acute myelogenous leukemia (diagnosis)", "Acute myeloid leukemia, M6 type (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute erythroid leukemia", "shortest_name_length": 2}
{"curie": "MONDO:0009747", "names": ["NN", "NNH", "MTDPS6", "NAVAJO NEUROPATHY", "Navajo neuropathy", "NAVAJO NEUROHEPATOPATHY", "Navajo neurohepatopathy", "Navajo neurohepatopathy (disorder)", "MPV17-Associated Hepatocerebral MDS", "Mitochondrial Dna Depletion Syndrome 6", "mitochondrial DNA depletion syndrome 6", "NAVAJO FAMILIAL NEUROGENIC ARTHROPATHY", "Navajo Familial Neurogenic Arthropathy", "Navajo familial neurogenic arthropathy", "MITOCHONDRIAL DNA DEPLETION SYNDROME 6 (HEPATOCEREBRAL TYPE)", "mitochondrial DNA depletion syndrome 6 (hepatocerebral type)", "MPV17-related hepatocerebral mitochondrial DNA depletion syndrome", "MPV17-Related Hepatocerebral Mitochondrial DNA Depletion Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial DNA depletion syndrome 6 (hepatocerebral type)", "shortest_name_length": 2}
{"curie": "MONDO:0012986", "names": ["BTOP", "Polymicrogyria, Bilateral Occipital", "bilateral temporooccipital polymicrogyria", "polymicrogyria, bilateral temporooccipital", "POLYMICROGYRIA, BILATERAL TEMPOROOCCIPITAL", "bilateral parasagittal parieto-occipital polymicrogyria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bilateral parasagittal parieto-occipital polymicrogyria", "shortest_name_length": 4}
{"curie": "MONDO:0003938", "names": ["Bladder Enteric Type Adenocarcinoma", "bladder colonic type adenocarcinoma", "Bladder Colonic Type Adenocarcinoma", "bladder enteric type adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder colonic type adenocarcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C1334273", "names": ["Invasive Breast Carcinoma by Histologic Grade", "Infiltrating Breast Carcinoma by Histologic Grade", "Invasive Breast Carcinoma by Nottingham Combined Histologic Grade", "Infiltrating Breast Carcinoma by Nottingham Combined Histologic Grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Invasive Breast Carcinoma by Histologic Grade", "shortest_name_length": 45}
{"curie": "MONDO:0009363", "names": ["Daish Hardman Lamont syndrome", "Daish-Hardman-Lamont syndrome", "hydrocephaly - tall stature - joint laxity", "Hydrocephaly-tall stature-joint laxity syndrome", "hydrocephaly-tall stature-joint laxity syndrome", "Hydrocephaly, tall stature, joint laxity syndrome", "Hydrocephalus, tall stature, joint laxity syndrome", "hydrocephalus, tall stature, joint laxity and kyphoscoliosis", "hydrocephalus, tall stature, JOINT laxity, and kyphoscoliosis", "HYDROCEPHALUS, TALL STATURE, JOINT LAXITY, AND KYPHOSCOLIOSIS", "Hydrocephalus, tall stature, joint laxity, and kyphoscoliosis", "Hydrocephalus, tall stature, joint laxity syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hydrocephaly-tall stature-joint laxity syndrome", "shortest_name_length": 29}
{"curie": "MONDO:0041959", "names": ["Fibrosis biliary", "biliary fibrosis", "fibrosis biliary", "FIBROSIS BILIARY", "Biliary fibrosis", "Biliary sclerosis", "Cholangiofibrosis", "biliary sclerosis", "fibrosis of bile duct", "Fibrosis of bile duct", "Biliary duct fibrosis", "biliary duct fibrosis", "Fibrosis of bile duct (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibrosis of bile duct", "shortest_name_length": 16}
{"curie": "MONDO:0009075", "names": ["PIERQUIN SYNDROME", "Pierquin syndrome", "DWM WITH POSTAXIAL POLYDACTYLY", "Dwm With Postaxial Polydactyly", "DWM with postaxial polydactyly", "Dandy Walker malformation postaxial polydactyly", "Dandy-Walker malformation with postaxial polydactyly", "DANDY-WALKER MALFORMATION WITH POSTAXIAL POLYDACTYLY", "Dandy-Walker malformation-postaxial polydactyly syndrome", "Dandy-Walker malformation with postaxial polydactyly syndrome", "Dandy-Walker malformation with postaxial polydactyly syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dandy-Walker malformation-postaxial polydactyly syndrome", "shortest_name_length": 17}
{"curie": "MONDO:0003363", "names": ["dermis cancer", "cancer of dermis", "malignant dermis tumor", "Malignant Dermis Tumor", "malignant dermis tumour", "malignant tumor of dermis", "malignant dermis neoplasm", "malignant dermal neoplasm", "Malignant tumor of dermis", "Malignant Tumor of Dermis", "Malignant Dermis Neoplasm", "Malignant Dermal Neoplasm", "malignant tumour of dermis", "Malignant tumour of dermis", "malignant neoplasm of Dermis", "Malignant Neoplasm of Dermis", "malignant neoplasm of dermis", "Malignant Tumor of the Dermis", "malignant tumor of the dermis", "skin neoplasm malignant dermis", "malignant neoplasm of the dermis", "Malignant Neoplasm of the Dermis", "Malignant tumor of dermis (disorder)", "malignant neoplasm of dermis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant dermis tumor", "shortest_name_length": 13}
{"curie": "MONDO:0003515", "names": ["fallopian tube teratoma", "Fallopian Tube Teratoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fallopian tube teratoma", "shortest_name_length": 23}
{"curie": "MONDO:0022904", "names": ["cryofibrinogenemia", "Cryofibrinogenemia", "cryofibrinogenaemia", "Cryofibrinogenaemia", "Cryofibrinogenemia, NOS", "Cryofibrinogenemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cryofibrinogenemia", "shortest_name_length": 18}
{"curie": "UMLS:C1318552", "names": ["nontraumatic epidural hemorrhage", "Nontraumatic epidural hemorrhage", "Nontraumatic epidural haemorrhage", "Nontraumatic extradural hemorrhage", "Nontraumatic extradural haemorrhage", "Non-Traumatic Extradural Hemorrhage", "hemorrhage; extradural, nontraumatic", "nontraumatic epidural hemorrhage (diagnosis)", "Nontraumatic extradural intracranial hemorrhage", "Nontraumatic extradural intracranial haemorrhage", "Nontraumatic extradural intracranial hemorrhage (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nontraumatic extradural hemorrhage", "shortest_name_length": 32}
{"curie": "MONDO:0003248", "names": ["adult pineal gland tumor", "Adult Pineal Gland Tumor", "Adult Pineal Gland Neoplasm", "adult pineal gland neoplasm", "pineal parenchymal cell tumor", "Pineal Parenchymal Cell Tumor", "Adult Pineal Parenchymal Tumor", "adult pineal parenchymal tumor", "pineal parenchymal tumor, adult", "parenchymal tumor, adult pineal", "tumor, adult pineal parenchymal", "adult Pineal Parenchymal neoplasm", "Adult Pineal Parenchymal Neoplasm", "adult pineal parenchymal neoplasm", "Adult Pineal Parenchymal Cell Tumor", "adult pineal parenchymal cell tumor", "adult pineal parenchymal cell neoplasm", "Adult Pineal Parenchymal Cell Neoplasm", "Parenchymal Tumor of Adult Pineal Gland", "parenchymal tumor of adult pineal gland", "parenchymal neoplasm of adult pineal gland", "pineal parenchymal cell neoplasm of adults", "Parenchymal Neoplasm of Adult Pineal Gland", "parenchymal tumor of the adult pineal gland", "Parenchymal Tumor of the Adult Pineal Gland", "Brain tumor, adult: Pineal parenchymal tumors", "parenchymal neoplasm of the adult pineal gland", "Parenchymal Neoplasm of the Adult Pineal Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult pineal parenchymal tumor", "shortest_name_length": 24}
{"curie": "MONDO:0008837", "names": ["Ataxia, Deafness, and Cardiomyopathy", "ATAXIA, DEAFNESS, AND CARDIOMYOPATHY", "ataxia, deafness, and cardiomyopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ataxia, deafness, and cardiomyopathy", "shortest_name_length": 36}
{"curie": "MONDO:0007296", "names": ["SCA31", "spinocerebellar ataxia 31", "SPINOCEREBELLAR ATAXIA 31", "Spinocerebellar Ataxia 31", "Spinocerebellar Ataxia Type 31", "spinocerebellar ataxia type 31", "Spinocerebellar ataxia type 31", "SCA31 Spinocerebellar Ataxia 31", "spinocerebellar ataxia 16q22-linked", "SPINOCEREBELLAR ATAXIA, 16q22-LINKED", "spinocerebellar ataxia, 16Q22-linked", "SPINOCEREBELLAR ATAXIA 31 (disorder)", "Spinocerebellar Ataxia, 16q22-Linked", "Spinocerebellar ataxia type 31 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia type 31", "shortest_name_length": 5}
{"curie": "MONDO:0020473", "names": ["dappled diaphyseal dysplasia", "Dappled diaphyseal dysplasia", "Dappled diaphyseal dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dappled diaphyseal dysplasia", "shortest_name_length": 28}
{"curie": "MONDO:0016954", "names": ["Trisomy 3q", "trisomy 3q", "3q+ syndrome", "Duplication 3q", "dup(3q) syndrome", "partial trisomy 3q", "3q duplication syndrome", "duplication 3q syndrome", "Chromosome 3, trisomy 3q", "chromosome 3, trisomy 3q", "chromosome 3q duplication", "chromosome 3q trisomy syndrome", "partial trisomy of chromosome 3q", "chromosome 3q duplication syndrome", "partial duplication of chromosome 3q", "partial duplication of the long arm of chromosome 3", "partial duplication of the long arm of chromosome type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of the long arm of chromosome 3", "shortest_name_length": 10}
{"curie": "UMLS:C5557262", "names": ["Metastatic Breast Inflammatory Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Breast Inflammatory Carcinoma", "shortest_name_length": 40}
{"curie": "UMLS:C4518377", "names": ["hemangiopericytoma benign", "Benign Hemangiopericytoma", "Benign hemangiopericytoma", "benign hemangiopericytoma", "Hemangiopericytoma, benign", "HEMANGIOPERICYTOMA, BENIGN", "Benign haemangiopericytoma", "Haemangiopericytoma, benign", "Solitary fibrous tumor/hemangiopericytoma grade 1", "Solitary fibrous tumour/haemangiopericytoma grade 1", "Solitary fibrous tumor and hemangiopericytoma grade 1", "Solitary fibrous tumour and haemangiopericytoma grade 1", "Solitary fibrous tumor and hemangiopericytoma grade 1 (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Solitary fibrous tumor and hemangiopericytoma grade 1", "shortest_name_length": 25}
{"curie": "UMLS:C1332529", "names": ["Benign thecoma", "THECOMA, BENIGN", "Benign Ovarian Thecoma", "Benign theca cell tumor", "Benign Thecoma of Ovary", "Benign theca cell tumour", "Thecal Cell Tumor, Benign", "Benign Thecoma of the Ovary", "Benign Ovarian Thecal Cell Tumor", "Benign Thecal Cell Tumor of Ovary", "Benign Ovarian Thecal Cell Neoplasm", "Benign Thecal Cell Neoplasm of Ovary", "Benign Thecal Cell Tumor of the Ovary", "Benign Thecal Cell Neoplasm of the Ovary", "Benign thecoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign thecoma", "shortest_name_length": 14}
{"curie": "UMLS:C0584995", "names": ["Impaired writing", "Writing impaired", "WRITING IMPAIRED", "difficulty writing", "Difficulty writing", "Writing difficulties", "Difficulty writing (finding)", "difficulty writing (symptom)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Difficulty writing", "shortest_name_length": 16}
{"curie": "MONDO:0013304", "names": ["VWD2", "VWD type 2", "VWD, TYPE 2", "VWD, type 2", "von Willebrand disease 2", "von willebrand's disease 2", "von Willebrand's disease 2", "Von Willebrand disease type 2", "Type 2 von Willebrand Disease", "von Willebrand disease type 2", "Von Willebrand disease, type 2", "Type II von Willebrand Disease", "von Willebrand disease type II", "VON WILLEBRAND DISEASE, TYPE 2", "von Willebrand Disease, Type 2", "VON WILLEBRAND disease, type 2", "von Willebrand Disease, Type II", "Von Willebrand disease, type 2M", "von Willebrand's disease type 2", "Von Willebrand disease, type 2B", "VON WILLEBRAND DISEASE, TYPE II", "Von Willebrand disease, type 2N", "Von Willebrand disease, type 2A", "Hereditary von Willebrand disease type 2", "von Willebrand disease type 2 (diagnosis)", "Von Willebrand disease, type 2, unspecified", "von Willebrand disease, types 2A, 2B, 2M, and 2N", "Hereditary von Willebrand disease type 2 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "von Willebrand disease 2", "shortest_name_length": 4}
{"curie": "MONDO:0032613", "names": ["MC1DN8", "nuclear type mitochondrial complex I deficiency 8", "mitochondrial complex 1 deficiency, nuclear type 8", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 8", "shortest_name_length": 6}
{"curie": "MONDO:0008922", "names": ["MTDPS10", "SENGERS SYNDROME", "Sengers syndrome", "Cardiomyopathy and cataract", "Cataract and cardiomyopathy", "cardiomyopathy and cataract", "cataract and cardiomyopathy", "CARDIOMYOPATHY AND CATARACT", "mitochondrial DNA depletion syndrome 10", "cardiomyopathic mitochondrial DNA depletion syndrome 10", "mitochondrial DNA depletion syndrome 10 (Cardiomyopathic type)", "MITOCHONDRIAL DNA DEPLETION SYNDROME 10 (CARDIOMYOPATHIC TYPE)", "mitochondrial DNA depletion syndrome 10 (cardiomyopathic type)", "congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome", "Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome", "Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome", "Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sengers syndrome", "shortest_name_length": 7}
{"curie": "UMLS:C1333932", "names": ["HTLV-1 Related Malignancy", "HTLV-1-Related Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HTLV-1-Related Malignant Neoplasm", "shortest_name_length": 25}
{"curie": "UMLS:C0342634", "names": ["Neonatal hypocalcemia", "neonatal hypocalcemia", "Neonatal hypocalcaemia", "hypocalcemia; neonatal", "neonatal; hypocalcemia", "Neonatal hypocalcemia (disorder)", "neonatal hypocalcemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neonatal hypocalcemia", "shortest_name_length": 21}
{"curie": "UMLS:C0677686", "names": ["Stage II Indolent Non-Hodgkin Lymphoma", "Stage II Contiguous Adult Indolent Non-Hodgkin Lymphoma", "stage II contiguous adult indolent non-Hodgkin lymphoma", "indolent, contiguous stage II adult non-Hodgkin lymphoma", "Indolent Contiguous Stage II Adult Non-Hodgkin's Lymphoma", "indolent adult contiguous stage II non-Hodgkin's lymphoma", "Adult Indolent Contiguous Non-Hodgkin's Lymphoma Stage II", "stage II contiguous adult indolent non-Hodgkin's lymphoma", "indolent contiguous stage II adult non-Hodgkin's lymphoma", "indolent adult contiguous non-Hodgkin's lymphoma stage II", "stage II indolent adult contiguous non-Hodgkin's lymphoma", "Indolent Adult Contiguous Stage II Non-Hodgkin's Lymphoma", "Stage II Indolent Adult Contiguous Non-Hodgkin's Lymphoma", "adult indolent contiguous non-Hodgkin's lymphoma stage II", "Stage II Contiguous Adult Indolent Non-Hodgkin's Lymphoma", "Indolent Adult Contiguous Non-Hodgkin's Lymphoma Stage II", "Ann Arbor Stage II Contiguous Adult Indolent Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Contiguous Adult Indolent Non-Hodgkin Lymphoma", "shortest_name_length": 38}
{"curie": "UMLS:C1336271", "names": ["Stage III Small Cell Lung Cancer", "Stage III Small Cell Lung Carcinoma", "Stage III Small Cell Carcinoma of Lung", "Stage III Small Cell Carcinoma of the Lung", "Stage III Small Cell Lung Carcinoma AJCC v7", "Stage III Lung Small Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Lung Small Cell Carcinoma AJCC v7", "shortest_name_length": 32}
{"curie": "UMLS:C4520742", "names": ["Stage IV Salivary Gland Cancer", "stage IV salivary gland cancer", "Stage IV Major Salivary Gland Cancer", "Stage IV Major Salivary Gland Carcinoma", "Stage IV Carcinoma of Major Salivary Gland", "Stage IV Major Salivary Gland Cancer AJCC v7", "Stage IV Carcinoma of the Major Salivary Gland", "Stage IV Major Salivary Gland Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Major Salivary Gland Cancer AJCC v7", "shortest_name_length": 30}
{"curie": "UMLS:C1518380", "names": ["Non-Neoplastic, Non-Molar Trophoblastic Disorder", "Non-Neoplastic, Non-Molar Gestational Trophoblastic Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic, Non-Molar Gestational Trophoblastic Disorder", "shortest_name_length": 48}
{"curie": "MONDO:0022899", "names": ["crawfurd syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "crawfurd syndrome", "shortest_name_length": 17}
{"curie": "UMLS:C1332642", "names": ["Burkitt-like Lymphoma PTLD", "Burkitt's-like Lymphoma PTLD", "Burkitt-Like Lymphoma Post-Transplant Lymphoproliferative Disorder", "Burkitt's-Like Lymphoma Post-Transplant Lymphoproliferative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Burkitt-Like Lymphoma Post-Transplant Lymphoproliferative Disorder", "shortest_name_length": 26}
{"curie": "MONDO:0019258", "names": ["mPKU", "mild PKU", "variant PKU", "mild phenylketonuria", "variant phenylketonuria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mild phenylketonuria", "shortest_name_length": 4}
{"curie": "UMLS:C5419159", "names": ["Recurrent Endogenous Cushing Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Endogenous Cushing Syndrome", "shortest_name_length": 37}
{"curie": "UMLS:C0268734", "names": ["Acute nephropathy", "nephropathy acute", "Acute nephropathy, NOS", "Acute nephropathy (disorder)", "Acute nephropathy (diagnosis)", "Nephropathy specified as acute"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute nephropathy", "shortest_name_length": 17}
{"curie": "MONDO:0005778", "names": ["haemonchiasis", "Haemonchiases", "Haemonchiasis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "haemonchiasis", "shortest_name_length": 13}
{"curie": "UMLS:C3272317", "names": ["Stent restenosis", "In Stent Restenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stent restenosis", "shortest_name_length": 16}
{"curie": "UMLS:C0340464", "names": ["ectopics", "Ectopics", "ectopic beat", "EXTRASYSTOLE", "Extrasystole", "extrasystole", "extrasystoles", "Ectopic beats", "EXTRASYSTOLES", "Extrasystoles", "ectopic beats", "beat; ectopic", "ECTOPIC BEATS", "beats ectopic", "ectopic rhythm", "premature beat", "Premature Beat", "beats; ectopia", "ectopia; beats", "Ectopic rhythm", "premature; beat", "premature beats", "beat; premature", "Beat, Premature", "Premature beats", "Premature Beats", "beats; premature", "Beats, Premature", "premature; beats", "Extrasystoles NOS", "ectopic heartbeat", "Ectopic Heartbeat", "ectopic heartbeats", "Heartbeats ectopic", "Ectopic heartbeats", "HEARTBEATS ECTOPIC", "Heartbeat, Ectopic", "Ectopic Heartbeats", "Ectopic rhythm, NOS", "EXTRASYSTOLES (NOS)", "premature heartbeat", "Heartbeats, Ectopic", "heartbeat premature", "Premature heartbeat", "arrhythmia; ectopic", "ectopic; heart beat", "Premature beats NOS", "premature heartbeats", "Heartbeats premature", "Premature beats, NOS", "HEARTBEATS PREMATURE", "Ectopic rhythm disorder", "Rhythm disorder, ectopic", "extrasystole (diagnosis)", "Ectopic beats (disorder)", "arrhythmia extrasystolic", "Extrasystolic arrhythmia", "Premature Cardiac Complex", "Heartbeat (pulse);ectopic", "Extrasystolic arrhythmias", "arrhythmia; extrasystolic", "extrasystolic; arrhythmia", "Ectopic rhythm (disorder)", "ectopic beats (diagnosis)", "Cardiac Complex, Premature", "Premature beats (disorder)", "Ectopic rhythm abnormality", "Ectopic rhythm (diagnosis)", "Premature Cardiac Complices", "Heartbeat (pulse);premature", "Premature Cardiac Complexes", "cardiac arrhythmia; ectopic", "complexes premature cardiac", "heart; contraction premature", "Premature beats, unspecified", "heart; premature contraction", "Complexes, Premature Cardiac", "Cardiac Complexes, Premature", "contraction; premature, heart", "cardiac arrhythmia; extrasystolic", "cardiac conduction system ectopic rhythm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Premature Cardiac Complex", "shortest_name_length": 8}
{"curie": "MONDO:0007555", "names": ["EBSOG", "EBS5A", "EBS-O", "Ebs-Og", "EBS-Og", "Epidermolysis bullosa simplex 1", "Epidermolysis bullosa simplex of Ogna", "epidermolysis bullosa simplex Ogna type", "EPIDERMOLYSIS BULLOSA SIMPLEX, OGNA TYPE", "epidermolysis bullosa simplex, Ogna type", "Epidermolysis bullosa simplex, Ogna type", "pidermolysis bullosa simplex 5A, Ogna type", "EPIDERMOLYSIS BULLOSA SIMPLEX 5A, OGNA TYPE", "epidermolysis bullosa simplex 5A, Ogna type", "Epidermolysis bullosa simplex, Ogna type (disorder)", "PLEC-related intermediate EBS without extracutaneous involvement", "PLEC-related intermediate epidermolysis bullosa simplex without extracutaneous involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pidermolysis bullosa simplex 5A, Ogna type", "shortest_name_length": 5}
{"curie": "MONDO:0008135", "names": ["OPA13", "Optic Atrophy with Negative Electroretinograms", "optic atrophy with negative Electroretinograms", "optic atrophy 13 with retinal and foveal abnormalities", "OPTIC ATROPHY 13 WITH RETINAL AND FOVEAL ABNORMALITIES", "OPTIC ATROPHY WITH NEGATIVE ELECTRORETINOGRAMS, FORMERLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "optic atrophy 13 with retinal and foveal abnormalities", "shortest_name_length": 5}
{"curie": "MONDO:0014094", "names": ["AHMIO2", "severe congenital hypochromic sideroblastic anemia", "Severe congenital hypochromic sideroblastic anemia", "Severe congenital hypochromic sideroblastic anaemia", "ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 2", "anemia, hypochromic microcytic, with iron overload 2", "anemia, hypochromic microcytic, with iron overload type 2", "severe congenital hypochromic anemia with ringed sideroblasts", "Severe congenital hypochromic anemia with ringed sideroblasts", "Severe congenital hypochromic anaemia with ringed sideroblasts", "Severe congenital hypochromic anemia with ringed sideroblasts (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe congenital hypochromic anemia with ringed sideroblasts", "shortest_name_length": 6}
{"curie": "UMLS:C5556338", "names": ["Recurrent Myxoid Glioneuronal Tumor", "Recurrent Myxoid Glioneuronal Tumor, PDGFRA p.K385-Mutant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Myxoid Glioneuronal Tumor", "shortest_name_length": 35}
{"curie": "MONDO:0010672", "names": ["MCOPS7", "LSDMCA1", "MLS syndrome", "MIDAS syndrome", "Micropthalmia syndromic 7", "Microphthalmia, syndromic 7", "syndromic microphthalmia type 7", "microphthalmia with linear skin defects syndrome", "microphthalmia-dermal aplasia-sclerocornea syndrome", "linear skin defects with multiple congenital anomalies", "microphthalmia dermal aplasia and sclerocornea syndrome", "linear skin defects with multiple congenital anomalies 1", "linear skin defects with multiple congenital anomalies type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "linear skin defects with multiple congenital anomalies", "shortest_name_length": 6}
{"curie": "MONDO:0012059", "names": ["PAPA4", "Papa4", "Postaxial Polydactyly, Type A4", "POSTAXIAL POLYDACTYLY, TYPE A4", "postaxial polydactyly, type A4", "POLYDACTYLY, POSTAXIAL, TYPE A4", "Polydactyly, Postaxial, Type A4", "polydactyly, postaxial, type A4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polydactyly, postaxial, type A4", "shortest_name_length": 5}
{"curie": "UMLS:C0269993", "names": ["Lactation;suppressed", "Suppressed lactation", "suppressed lactation", "Lactation suppressed", "Lactation, suppressed", "lactation; suppression", "suppression; lactation", "Suppressed lactation (disorder)", "suppressed lactation (diagnosis)", "Suppressed lactation, unspecified as to episode of care", "Suppressed lactation, unspecified as to episode of care or not applicable"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Suppressed lactation", "shortest_name_length": 20}
{"curie": "MONDO:0012919", "names": ["T1D20", "IDDM20", "type 1 diabetes mellitus 20", "TYPE 1 DIABETES MELLITUS 20", "HNF1A type 1 diabetes mellitus", "insulin-dependent diabetes mellitus 20", "Insulin-Dependent Diabetes Mellitus 20", "Diabetes Mellitus, Insulin-Dependent, 20", "diabetes mellitus, insulin-dependent, 20", "DIABETES MELLITUS, INSULIN-DEPENDENT, 20", "diabetes mellitus, insulin-dependent, type 20", "DIABETES MELLITUS, INSULIN-DEPENDENT, 20 (disorder)", "type 1 diabetes mellitus caused by mutation in HNF1A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type 1 diabetes mellitus 20", "shortest_name_length": 5}
{"curie": "MONDO:0001812", "names": ["parasitic eyelid infestation", "Parasitic eyelid infestation", "Parasitic infestation of eyelid", "parasitic infestation of eyelid", "Parasitic eyelid infestation (disorder)", "parasitic infestation of eyelid (diagnosis)", "infestation; parasite, parasitic, eyelid (etiology)", "infestation; parasite, parasitic, eyelid (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parasitic eyelid infestation", "shortest_name_length": 28}
{"curie": "MONDO:0009996", "names": ["RHIZOMELIC SYNDROME", "Rhizomelic syndrome", "rhizomelic syndrome", "Familial rhizomelic dysplasia", "familial rhizomelic dysplasia", "RHIZOMELIC DYSPLASIA, FAMILIAL", "rhizomelic dysplasia, familial", "Rhizomelic dysplasia, familial", "rhizomelic syndrome, Urbach type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rhizomelic syndrome, Urbach type", "shortest_name_length": 19}
{"curie": "MONDO:0011917", "names": ["FSGS3", "focal segmental glomerulosclerosis 3", "glomerulosclerosis, focal segmental, 3", "CD2AP focal segmental glomerulosclerosis", "susceptibility to focal segmental glomerulosclerosis 3", "FOCAL SEGMENTAL GLOMERULOSCLEROSIS 3, SUSCEPTIBILITY TO", "focal segmental glomerulosclerosis 3, susceptibility to", "GLOMERULOSCLEROSIS, FOCAL SEGMENTAL, 3, SUSCEPTIBILITY TO", "glomerulosclerosis, focal segmental, 3, susceptibility to", "focal segmental glomerulosclerosis caused by mutation in CD2AP"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal segmental glomerulosclerosis 3, susceptibility to", "shortest_name_length": 5}
{"curie": "UMLS:C1542107", "names": ["Digestive System Carcinoma In Situ", "Gastrointestinal carcinoma in situ", "Gastrointestinal carcinoma in situ NOS", "Gastrointestinal System Carcinoma In Situ"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal carcinoma in situ", "shortest_name_length": 34}
{"curie": "UMLS:C2981613", "names": ["Stage IIIA Digestive System Neuroendocrine Tumor", "Stage IIIA Gastrointestinal Neuroendocrine Neoplasm", "Stage IIIA Digestive System Neuroendocrine Neoplasm", "Stage IIIA Digestive System Neuroendocrine Tumor AJCC v7", "Stage IIIA Digestive System Neuroendocrine Neoplasm AJCC v7", "Stage IIIA Gastrointestinal Neuroendocrine Neoplasm AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Digestive System Neuroendocrine Tumor AJCC v7", "shortest_name_length": 48}
{"curie": "MONDO:0100047", "names": ["basal cell carcinoma, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "basal cell carcinoma, susceptibility to", "shortest_name_length": 39}
{"curie": "MONDO:0006916", "names": ["post cholecystectomy", "Postcholecystectomy Syndrome", "Postcholecystectomy syndrome", "postcholecystectomy syndrome", "POSTCHOLECYSTECTOMY SYNDROME", "Post-Cholecystectomy Syndrome", "syndrome; postcholecystectomy", "postcholecystectomy; syndrome", "post-cholecystectomy syndrome", "Postcholecystectomy Syndromes", "Post cholecystectomy syndrome", "post cholecystectomy syndrome", "Syndrome, Postcholecystectomy", "Post-cholecystectomy syndrome", "Post Cholecystectomy Syndrome", "Syndrome, Post-Cholecystectomy", "Syndromes, Postcholecystectomy", "Post-Cholecystectomy Syndromes", "Syndromes, Post-Cholecystectomy", "post cholecystectomy (diagnosis)", "Postcholecystectomy syndrome (disorder)", "postcholecystectomy syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postcholecystectomy syndrome", "shortest_name_length": 20}
{"curie": "MONDO:0017007", "names": ["partial deletion of chromosome Xq", "partial monosomy of chromosome Xq", "partial monosomy of the long arm of chromosome X", "partial deletion of the long arm of chromosome X", "partial deletion of the long arm of chromosome type X"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of the long arm of chromosome X", "shortest_name_length": 33}
{"curie": "UMLS:C5420853", "names": ["Ciliary Body Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ciliary Body Adenocarcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C4329654", "names": ["Cervical, Thoracic, and Lumbosacral Spinal Cord Ependymal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical, Thoracic, and Lumbosacral Spinal Cord Ependymal Tumor", "shortest_name_length": 63}
{"curie": "UMLS:C5421215", "names": ["Regional lymph node (metastasis)", "Metastatic Malignant Neoplasm in the Regional Lymph Nodes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Malignant Neoplasm in the Regional Lymph Nodes", "shortest_name_length": 32}
{"curie": "UMLS:C1263836", "names": ["Neonatal infectious disorder", "Neonatal Infectious Disorder", "neonatal infectious disorder", "Neonatal infectious disorder (disorder)", "neonatal infectious disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neonatal infectious disorder", "shortest_name_length": 28}
{"curie": "UMLS:C1519922", "names": ["Vaginal Keratinizing Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Keratinizing Squamous Cell Carcinoma", "shortest_name_length": 44}
{"curie": "UMLS:C3650625", "names": ["abnormal uterine bleeding", "Abnormal uterine bleeding", "Abnormal uterine hemorrhage", "Abnormal uterine haemorrhage", "Dysfunctional uterine bleeding", "Abnormal uterine bleeding (disorder)", "abnormal uterine bleeding (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abnormal uterine bleeding", "shortest_name_length": 25}
{"curie": "MONDO:0006270", "names": ["LCIS", "lcis", "LCIS, NOS", "lobular carcinoma in situ", "Lobular carcinoma in-situ", "Lobular Carcinoma in situ", "lobular carcinoma in-situ", "Lobular Carcinoma In Situ", "Lobular carcinoma in situ", "Lobular Ca in situ of Breast", "lobular Ca in situ of breast", "Lobular carcinoma in situ, NOS", "LCIS, Lobular Carcinoma In Situ", "LCIS - Lobular carcinoma in situ", "lobular Ca in situ of the breast", "Lobular Ca in situ of the Breast", "Breast Lobular Carcinoma In Situ", "lobular breast carcinoma in situ", "Lobular Carcinoma In Situ (LCIS)", "lobular carcinoma in situ (LCIS)", "Lobular Breast Carcinoma In Situ", "breast lobular carcinoma in situ", "Lobular carcinoma, noninfiltrating", "Non-Infiltrating Lobular Carcinoma", "Non-infiltrating lobular carcinoma", "non-infiltrating lobular carcinoma", "lobular carcinoma in situ of breast", "Lobular carcinoma, non-infiltrating", "Lobular Carcinoma in situ of Breast", "non-invasive lobular breast carcinoma", "Non-Invasive Lobular Breast Carcinoma", "Lobular Carcinoma In Situ of the Breast", "lobular carcinoma in situ of the breast", "Non-Invasive Lobular Carcinoma of Breast", "non-invasive lobular carcinoma of breast", "Non-Infiltrating Lobular Breast Carcinoma", "non-infiltrating lobular breast carcinoma", "Non-Infiltrating Lobular Carcinoma of Breast", "Non-Invasive Lobular Carcinoma of the Breast", "non-infiltrating lobular carcinoma of breast", "non-invasive lobular carcinoma of the breast", "lobular carcinoma in situ of the breast (LCIS)", "Lobular Carcinoma In Situ of the Breast (LCIS)", "Non-Infiltrating Lobular Carcinoma of the Breast", "non-infiltrating lobular carcinoma of the breast", "Lobular carcinoma in situ (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lobular breast carcinoma in situ", "shortest_name_length": 4}
{"curie": "MONDO:0002169", "names": ["read", "carcinoma rectal", "rectum carcinoma", "carcinoma rectum", "rectal carcinoma", "carcinoma of rectum", "adenocarcinoma rectum", "rectum adenocarcinoma", "adenocarcinoma rectal", "Rectal Adenocarcinoma", "Rectal adenocarcinoma", "rectal adenocarcinoma", "RECTUM, ADENOCARCINOMA", "adenocarcinoma - rectum", "Adenocarcinoma - rectum", "Adenocarcinoma of rectum", "adenocarcinoma of rectum", "Adenocarcinoma of Rectum", "Adenocarcinoma of the rectum", "Adenocarcinoma of the Rectum", "adenocarcinoma of the rectum", "rectum cancer, adenocarcinoma", "RECTAL CANCER, ADENOCARCINOMA", "rectum, adenocarcinoma of the", "rectal, adenocarcinoma of the", "rectal cancer, adenocarcinoma", "Adenocarcinoma of rectum (disorder)", "adenocarcinoma of rectum (diagnosis)", "rectal neoplasm malignant adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rectum adenocarcinoma", "shortest_name_length": 4}
{"curie": "UMLS:C0751856", "names": ["mad hatter disease", "Mad Hatter Disease", "mad hatters disease", "Mad Hatter Diseases", "Mad Hatters Disease", "Mad Hatter's Disease", "mad hatter's disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mad Hatter Disease", "shortest_name_length": 18}
{"curie": "MONDO:0013679", "names": ["SOST2", "sclerosteosis 2", "SCLEROSTEOSIS 2", "LRP4 sclerosteosis", "sclerosteosis type 2", "sclerosteosis caused by mutation in LRP4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sclerosteosis 2", "shortest_name_length": 5}
{"curie": "UMLS:C0855072", "names": ["Relapsed Synovial Sarcoma", "Synovial Sarcoma Recurrent", "Recurrent Synovial Sarcoma", "Synovial sarcoma recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Synovial sarcoma recurrent", "shortest_name_length": 25}
{"curie": "MONDO:0019830", "names": ["congenital anomaly of the IVC", "Congenital anomaly of the IVC", "Inferior vena cava abnormality", "Inferior caval vein abnormality", "IVC - Inferior vena cava abnormality", "ICV - Inferior caval vein abnormality", "Congenital anomaly of inferior vena cava", "congenital anomaly of inferior vena cava", "congenital anomaly of the inferior vena cava", "Congenital anomaly of the inferior vena cava", "congenital anomaly of the inferior caval vein", "Congenital anomaly of inferior vena cava, NOS", "Congenital anomaly of the inferior caval vein", "Congenital anomaly of inferior vena cava (disorder)", "congenital anomaly of inferior vena cava (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital anomaly of the inferior vena cava", "shortest_name_length": 29}
{"curie": "UMLS:C3502132", "names": ["Adrenal Insufficiency, Congenital, With 46,Xy Sex Reversal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adrenal Insufficiency, Congenital, With 46,Xy Sex Reversal", "shortest_name_length": 58}
{"curie": "MONDO:0010096", "names": ["Tardive dystonia", "Tardive Dystonia", "Tardive Dystonias", "Dystonia, Tardive", "Dystonias, Tardive", "Dyskinesia tardive", "DYSKINESIA TARDIVE", "tardive dyskinesia", "Tardive dyskinesia", "dyskinesia tardive", "Tardive Dyskinesia", "TARDIVE DYSKINESIA", "dyskinesias tardive", "Tardive Dyskinesias", "Dyskinesia, Tardive", "Dyskinesias, Tardive", "TD - Tardive dyskinesia", "tardive dyskinesia (disease)", "Tardive dyskinesia (disorder)", "tardive dyskinesia (diagnosis)", "Drug-induced tardive dyskinesia", "drug-induced tardive dyskinesia", "drug-induced tardive dyskinesia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tardive dyskinesia", "shortest_name_length": 16}
{"curie": "MONDO:0005745", "names": ["Enoplida Infection", "Infection, Enoplida", "Enoplida Infections", "Infections, Enoplida", "Enoplea infectious disease", "Enoplea disease or disorder", "Enoplea caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Enoplea infectious disease", "shortest_name_length": 18}
{"curie": "UMLS:C1332334", "names": ["Aromatic Dyes-Related Cancer", "Aromatic Dyes-Related Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aromatic Dyes-Related Malignant Neoplasm", "shortest_name_length": 28}
{"curie": "UMLS:C1112243", "names": ["Phlebitis infective", "Infective Phlebitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infective Phlebitis", "shortest_name_length": 19}
{"curie": "MONDO:0008409", "names": ["SPMM", "SPMD", "MYH7-related late-onset SPMD", "scapuloperoneal muscular dystrophy", "Scapuloperoneal muscular dystrophy", "Scapuloperoneal Muscular Dystrophy", "SCAPULOPERONEAL MUSCULAR DYSTROPHY", "Muscular Dystrophy, Scapuloperoneal", "MYH7-related scapuloperoneal myopathy", "MYH7-Related Scapuloperoneal Myopathy", "Scapuloperoneal Myopathy, MYH7-Related", "Myopathy, MYH7-Related Scapuloperoneal", "SCAPULOPERONEAL MYOPATHY, MYH7-RELATED", "scapuloperoneal myopathy, MYH7-related", "Scapuloperoneal Myopathy, MYH7 Related", "scapuloperoneal syndrome, myopathic type", "SCAPULOPERONEAL SYNDROME, MYOPATHIC TYPE", "Scapuloperoneal muscular dystrophy (disorder)", "MYH7-related late-onset scapuloperoneal syndrome", "MYH7-related late-onset scapuloperoneal muscular dystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MYH7-related late-onset scapuloperoneal muscular dystrophy", "shortest_name_length": 4}
{"curie": "MONDO:0020695", "names": ["atonic cerebral palsy", "Atonic Cerebral Palsy", "Cerebral Palsy, Atonic", "cerebral palsy hypotonic", "hypotonic cerebral palsy", "Hypotonic cerebral palsy", "Hypotonic Cerebral Palsy", "Cerebral Palsy, Hypotonic", "Hypotonic Cerebral Palsies", "Hypotonic cerebral palsy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotonic cerebral palsy", "shortest_name_length": 21}
{"curie": "MONDO:0002563", "names": ["Jejunal Somatostatinoma", "jejunal somatostatinoma", "Somatosatinoma of Jejunum", "Somatosatinoma of jejunum", "Delta cell tumor of jejunum", "Delta Cell Tumor of Jejunum", "Somatosatinoma of the jejunum", "Somatosatinoma of the Jejunum", "Delta cell tumor of the jejunum", "Delta Cell Tumor of the Jejunum", "jejunal somatostatin-producing NET", "Jejunal Somatostatin-Producing NET", "Jejunal Somatostatin Producing Tumor", "jejunal somatostatin producing tumor", "jejunal delta cell somatostatin producing tumor", "Jejunal Somatostatin-Producing Neuroendocrine Tumor", "jejunal somatostatin-producing neuroendocrine tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "jejunal somatostatinoma", "shortest_name_length": 23}
{"curie": "MONDO:0003844", "names": ["CNS Lipoma", "CNS lipoma", "lipoma of CNS", "Lipoma of CNS", "Lipoma of the CNS", "lipoma of the CNS", "central nervous system lipoma", "Central Nervous System Lipoma", "lipoma of central nervous system", "Lipoma of Central Nervous System", "lipoma of the central nervous system", "Lipoma of the Central Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system lipoma", "shortest_name_length": 10}
{"curie": "UMLS:C1299699", "names": ["Somnolence syndrome", "somnolence syndrome", "Somnolence Syndrome", "Somnolence syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Somnolence syndrome", "shortest_name_length": 19}
{"curie": "MONDO:0019980", "names": ["Bilateral renal hypoplasia", "renal hypoplasia bilateral", "Renal hypoplasia, bilateral", "renal hypoplasia, bilateral", "hypoplasia; kidney, bilateral", "Bilateral renal hypoplasia (disorder)", "renal hypoplasia, bilateral (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal hypoplasia, bilateral", "shortest_name_length": 26}
{"curie": "MONDO:0003402", "names": ["yolk sac tumor", "Orchidoblastoma", "testis yolk sac tumor", "endodermal-sinus tumor", "yolk Sac tumor of testis", "yolk sac tumor of testis", "Yolk Sac Tumor of Testis", "testicular yolk sac tumor", "Testicular Yolk Sac Tumor", "Testicular yolk sac tumor", "yolk sac tumor, testicular", "Testicular yolk sac tumour", "Yolk Sac Neoplasm of Testis", "yolk Sac neoplasm of testis", "testicular Yolk Sac neoplasm", "Testicular Yolk Sac Neoplasm", "Yolk Sac Tumor of the Testis", "testicular yolk Sac neoplasm", "yolk Sac tumor of the testis", "yolk sac tumor of the testis", "testis cancer, yolk sac tumor", "Yolk Sac Neoplasm of the Testis", "testicle cancer, yolk sac tumor", "yolk Sac neoplasm of the testis", "endodermal sinus tumor of testis", "Endodermal Sinus Tumor of Testis", "Testicular Endodermal Sinus Tumor", "testicular cancer, yolk sac tumor", "testicular endodermal sinus tumor", "Endodermal Sinus Neoplasm of Testis", "endodermal sinus neoplasm of testis", "Testicular Endodermal Sinus Neoplasm", "yolk sac tumor of testis (diagnosis)", "endodermal sinus tumor of the testis", "testicular endodermal sinus neoplasm", "Endodermal Sinus Tumor of the Testis", "Endodermal Sinus Neoplasm of the Testis", "endodermal sinus neoplasm of the testis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular yolk sac tumor", "shortest_name_length": 14}
{"curie": "MONDO:0009547", "names": ["Teebi Al-Saleh Hassoon syndrome", "Teebi-Al Saleh-Hassoon syndrome", "Macrosomia with lethal microphthalmia", "macrosomia with lethal microphthalmia", "macrosomia with microphthalmia, lethal", "MACROSOMIA WITH MICROPHTHALMIA, LETHAL", "Macrosomia with Microphthalmia, Lethal", "macrosomia microphthalmia cleft palate", "macrosomia-microphthalmia-cleft palate syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macrosomia-microphthalmia-cleft palate syndrome", "shortest_name_length": 31}
{"curie": "UMLS:C4744394", "names": ["Sellar Teratoma with Malignant Transformation", "Teratoma with Malignant Transformation of the Sellar Region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sellar Teratoma with Malignant Transformation", "shortest_name_length": 45}
{"curie": "MONDO:0034024", "names": ["EDS VI", "kyphoscoliotic EDS", "kyphoscoliotic Ehlers-Danlos syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kyphoscoliotic Ehlers-Danlos syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C2987504", "names": ["Stage II Gallbladder Cancer", "Stage II Gallbladder Cancer AJCC v7", "Stage II Gallbladder Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Gallbladder Cancer AJCC v7", "shortest_name_length": 27}
{"curie": "MONDO:0013859", "names": ["CATC5", "CTRCT38", "cataract 38", "CATARACT 38", "cataract type 38", "cataract 38, autosomal recessive", "AGK early-onset non-syndromic cataract", "autosomal recessive congenital cataract 5", "cataract, autosomal recessive congenital 5", "CATARACT, AUTOSOMAL RECESSIVE CONGENITAL 5", "early-onset non-syndromic cataract caused by mutation in AGK"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 38", "shortest_name_length": 5}
{"curie": "MONDO:0008671", "names": ["WS2", "Ws2", "WS2A", "Waardenburg syndrome type 2A", "Waardenburg Syndrome Type 2A", "Waardenburg syndrome, type 2A", "Waardenburg syndrome type IIA", "WAARDENBURG SYNDROME, TYPE 2A", "Waardenburg Syndrome Type IIA", "Waardenburg Syndrome, Type 2A", "Waardenburg Syndrome, Type IIA", "WAARDENBURG SYNDROME, TYPE IIA", "MITF Waardenburg syndrome type 2", "Waardenburg syndrome without dystopia canthorum", "Waardenburg Syndrome Without Dystopia Canthorum", "WAARDENBURG SYNDROME WITHOUT DYSTOPIA CANTHORUM", "Waardenburg syndrome type 2 caused by mutation in MITF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Waardenburg syndrome type 2A", "shortest_name_length": 3}
{"curie": "MONDO:0003782", "names": ["uterine epithelioid leiomyosarcoma", "Uterine Corpus Epithelioid Leiomyosarcoma", "body of uterus epithelioid leiomyosarcoma", "uterine corpus epithelioid leiomyosarcoma", "epithelioid leiomyosarcoma of body of uterus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine corpus epithelioid leiomyosarcoma", "shortest_name_length": 34}
{"curie": "MONDO:0020673", "names": ["Arterial Occlusion", "arterial occlusion", "arterial obstruction", "Arterial Obstruction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arterial occlusion", "shortest_name_length": 18}
{"curie": "UMLS:C3897748", "names": ["Recurrent Oligoastrocytoma", "Recurrent Childhood Oligoastrocytoma", "recurrent childhood oligoastrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Oligoastrocytoma", "shortest_name_length": 26}
{"curie": "MONDO:0017708", "names": ["mevalonate kinase deficiency", "Mevalonate Kinase Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mevalonate kinase deficiency", "shortest_name_length": 28}
{"curie": "MONDO:0013898", "names": ["kin", "KIN", "KMIN", "systemic karyomegaly", "Systemic karyomegaly", "FAN1 interstitial nephritis", "karyomegalic interstitial nephritis", "Karyomegalic Interstitial Nephritis", "Karyomegalic interstitial nephritis", "interstitial nephritis, karyomegalic", "INTERSTITIAL NEPHRITIS, KARYOMEGALIC", "KIN - karyomegalic interstitial nephritis", "Karyomegalic interstitial nephritis (disorder)", "Karyomegalic interstitial nephritis (diagnosis)", "interstitial nephritis caused by mutation in FAN1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "karyomegalic interstitial nephritis", "shortest_name_length": 3}
{"curie": "MONDO:0004359", "names": ["DELUSIONAL DISORDER", "Delusional Disorder", "delusional disorder", "Delusional disorder", "Delusional Disorders", "DELUSIONAL DISORDERS", "delusional disorders", "Disorder, Delusional", "Delusional disorders", "Disorders, Delusional", "Delusional disorder, NOS", "Delusional disorder (disorder)", "delusional disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "delusional disorder", "shortest_name_length": 19}
{"curie": "UMLS:C0949855", "names": ["Mitochondrial Electron Transport Chain Deficiencies", "Electron Transport Chain Deficiencies, Mitochondrial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Electron Transport Chain Deficiencies, Mitochondrial", "shortest_name_length": 51}
{"curie": "UMLS:C4054745", "names": ["IgA Nephropathy, Infection-associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "IgA Nephropathy, Infection-associated", "shortest_name_length": 37}
{"curie": "MONDO:0032643", "names": ["PCH12", "pontocerebellar hypoplasia type 12", "Pontocerebellar hypoplasia type 12", "pontocerebellar hypoplasia, type 12", "PONTOCEREBELLAR HYPOPLASIA, TYPE 12", "COASY-related pontocerebellar hypoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pontocerebellar hypoplasia, type 12", "shortest_name_length": 5}
{"curie": "MONDO:0007014", "names": ["vibriosis", "Vibriosis", "Vibrioses", "Vibrio Illness", "vibrio infection", "Vibrio Infection", "Vibrio Illnesses", "Infection, Vibrio", "Vibrio Infections", "Vibrio infections", "Infections, Vibrio", "Infection due to Vibrio", "vibrio infectious disease", "Vibrio infectious disease", "Vibrio disease or disorder", "Infection caused by Vibrio", "Vibrio caused disease or disorder", "Infection due to non-cholerae vibrio", "Infection caused by Vibrio (disorder)", "Infection caused by non-cholerae vibrio", "Infection caused by non-cholerae vibrio (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vibrio infectious disease", "shortest_name_length": 9}
{"curie": "MONDO:0020563", "names": ["DDLS", "DDLPS", "Dedifferentiated liposarcoma", "Dedifferentiated Liposarcoma", "dedifferentiated liposarcoma", "Dedifferentiated Liposarcomas", "dedifferentiated; liposarcoma", "liposarcoma; dedifferentiated", "Liposarcoma, Dedifferentiated", "[M] Dedifferentiated liposarcoma", "Dedifferentiated liposarcoma (disorder)", "dedifferentiated liposarcoma (diagnosis)", "Dedifferentiated liposarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dedifferentiated liposarcoma", "shortest_name_length": 4}
{"curie": "UMLS:C1512747", "names": ["Infiltrating Bladder Urothelial Carcinoma with Glandular Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infiltrating Bladder Urothelial Carcinoma with Glandular Differentiation", "shortest_name_length": 72}
{"curie": "UMLS:C0346203", "names": ["adenocarcinoma cervix situ", "Adenocarcinoma in situ;cervix", "adenocarcinoma cervix in situ", "adenocarcinoma in situ cervix", "Cervix Adenocarcinoma in situ", "Cervical Adenocarcinoma In Situ", "cervical adenocarcinoma in situ", "Adenocarcinoma in situ of Cervix", "adenocarcinoma in situ of cervix", "Adenocarcinoma in situ of cervix", "Cervix Uteri Adenocarcinoma in situ", "adenocarcinoma in situ of the cervix", "Adenocarcinoma in situ of the Cervix", "Uterine Cervix Adenocarcinoma in situ", "Cervical ACIS (adenocarcinoma in situ)", "Adenocarcinoma in situ of Cervix Uteri", "AIS - Adenocarcinoma in situ of cervix", "Adenocarcinoma in situ of Uterine Cervix", "Adenocarcinoma in situ of the Cervix Uteri", "Adenocarcinoma in situ of cervix (disorder)", "adenocarcinoma in situ of cervix (diagnosis)", "Adenocarcinoma in situ of the Uterine Cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Adenocarcinoma In Situ", "shortest_name_length": 26}
{"curie": "MONDO:0014254", "names": ["OFC2", "OTFCS2", "OTOFACIOCERVICAL SYNDROME 2", "otofaciocervical syndrome 2", "PAX1 otofaciocervical syndrome", "otofaciocervical syndrome type 2", "OTOFACIOCERVICAL SYNDROME 2 WITH T-CELL DEFICIENCY", "OTOFACIOCERVICAL SYNDROME 2, WITH T-CELL DEFICIENCY", "otofaciocervical syndrome caused by mutation in PAX1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "otofaciocervical syndrome 2", "shortest_name_length": 4}
{"curie": "MONDO:0021462", "names": ["Benign Rectal Tumor", "benign rectal tumor", "Benign Rectal Tumors", "benign rectal tumors", "Rectal Tumors, Benign", "rectal tumors, benign", "rectum benign neoplasm", "benign rectal neoplasm", "Benign Rectal Neoplasm", "Benign Tumor of Rectum", "rectal neoplasm benign", "benign tumor of rectum", "Benign tumor of rectum", "Benign tumour of rectum", "benign rectal neoplasms", "Benign Rectal Neoplasms", "rectal neoplasms, benign", "Rectal Neoplasms, Benign", "benign neoplasm of rectum", "Benign neoplasm of rectum", "Benign Neoplasm of Rectum", "Benign Tumor of the Rectum", "benign tumor of the rectum", "Benign Neoplasm of the Rectum", "benign neoplasm of the rectum", "Benign neoplasm of rectum (disorder)", "benign neoplasm of rectum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of rectum", "shortest_name_length": 19}
{"curie": "UMLS:C0001723", "names": ["affective psychoses", "PSYCHOSIS AFFECTIVE", "Psychosis affective", "psychosis affective", "Affective Psychoses", "affective psychosis", "Affective Psychosis", "Affective psychosis", "Psychosis;affective", "psychosis; affective", "Psychoses, Affective", "affective; psychosis", "Psychosis, affective", "Affective psychosis NOS", "affective disorder psychotic", "Psychotic Affective Disorder", "Disorder, Psychotic Affective", "Affective Disorder, Psychotic", "Psychotic Affective Disorders", "Affective psychosis (disorder)", "Affective Disorders, Psychotic", "Disorders, Psychotic Affective", "Affective psychosis (diagnosis)", "Unspecified affective psychosis", "Affective psychosis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Affective Disorders, Psychotic", "shortest_name_length": 19}
{"curie": "UMLS:C3888473", "names": ["Feeding tube site infection", "Medical device site infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Medical device site infection", "shortest_name_length": 27}
{"curie": "UMLS:C1535973", "names": ["Bone fragmentation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone fragmentation", "shortest_name_length": 18}
{"curie": "OMIM:615457", "names": ["BMIQ18", "OBESITY, SUSCEPTIBILITY TO", "BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 18"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 6}
{"curie": "MONDO:0010089", "names": ["ISOD", "Sulfocysteinuria", "sulfocysteinuria", "SULFOCYSTEINURIA", "Sulfite oxidase deficiency", "sulfite oxidase deficiency", "sulfite oxidase; deficiency", "Sulphite oxidase deficiency", "deficiency; sulfite oxidase", "isolated sulfite oxidase deficiency", "Isolated sulfite oxidase deficiency", "SULFITE OXIDASE DEFICIENCY, ISOLATED", "sulfite oxidase deficiency, isolated", "Sulfite oxidase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated sulfite oxidase deficiency", "shortest_name_length": 4}
{"curie": "UMLS:C0232933", "names": ["Abnormal menstrual cycle", "abnormal menstrual cycle", "Menstrual cycle abnormal", "abnormal cycles menstrual", "abnormal menstruation cycle", "Menstruation, abnormal cycle", "Abnormal menstrual cycle, NOS", "Abnormal menstrual cycle (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abnormal menstrual cycle", "shortest_name_length": 24}
{"curie": "MONDO:0030471", "names": ["GAMOS9", "GALLOWAY-MOWAT SYNDROME 9", "Galloway-Mowat syndrome 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Galloway-Mowat syndrome 9", "shortest_name_length": 6}
{"curie": "MONDO:0009548", "names": ["HOMG5", "FHHNCOI", "Meier-Blumberg-Imahorn syndrome", "Meier Blumberg Imahorn syndrome", "FHHNC WITH SEVERE OCULAR INVOLVEMENT", "FHHNC with severe ocular involvement", "bilateral macular coloboma with hypercalciuria", "Hypomagnesemia, Renal, with Ocular Involvement", "HYPOMAGNESEMIA, RENAL, WITH OCULAR INVOLVEMENT", "hypomagnesemia, renal, with ocular involvement", "renal hypomagnesemia 5 with ocular involvement", "Macular Coloboma, Bilateral, with Hypercalciuria", "macular coloboma, bilateral, with hypercalciuria", "MACULAR COLOBOMA, BILATERAL, WITH HYPERCALCIURIA", "HYPOMAGNESEMIA 5, RENAL, WITH OCULAR INVOLVEMENT", "Hypomagnesemia 5, Renal, with Ocular Involvement", "hypomagnesemia 5, renal, with ocular involvement", "Hypercalciuria-bilateral macular coloboma syndrome", "hypercalciuria-bilateral macular coloboma syndrome", "Idiopathic hypercalciuria with bilateral macular colobomata", "HYPOMAGNESEMIA 5, RENAL, WITH OR WITHOUT OCULAR INVOLVEMENT", "idiopathic hypercalciuria with bilateral macular colobomata", "Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement", "Familial hypomagnesaemia hypercalciuria nephrocalcinosis with severe ocular involvement", "familial hypomagnesemia with hypercalciuria, nephrocalcinosis and severe ocular involvement", "Hypomagnesemia, Familial, with Hypercalciuria, Nephrocalcinosis, and Severe Ocular Involvement", "HYPOMAGNESEMIA, FAMILIAL, WITH HYPERCALCIURIA, NEPHROCALCINOSIS, AND SEVERE OCULAR INVOLVEMENT", "hypomagnesemia, familial, with hypercalciuria, nephrocalcinosis, and severe ocular involvement", "Primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement", "Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement (disorder)", "familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal hypomagnesemia 5 with ocular involvement", "shortest_name_length": 5}
{"curie": "MONDO:0009227", "names": ["CGF", "IMF1", "myofibromatosis", "juvenile fibromatosis", "Juvenile fibromatosis", "PDGFRB myofibromatosis", "Myofibromatosis, Juvenile", "infantile myofibromatosis", "MYOFIBROMATOSIS, JUVENILE", "myofibromatosis, juvenile", "Infantile Myofibromatosis", "Infantile myofibromatosis", "Myofibromatosis, Infantile", "Infantile Myofibromatosis 1", "MYOFIBROMATOSIS, INFANTILE, 1", "myofibromatosis, infantile, 1", "myofibromatosis, infantile, type 1", "Congenital generalized fibromatosis", "Congenital generalised fibromatosis", "Generalized congenital fibromatosis", "Fibromatosis, Congenital Generalized", "Infantile myofibromatosis (disorder)", "FIBROMATOSIS, CONGENITAL GENERALIZED", "fibromatosis, congenital generalized", "infantile myofibromatosis (diagnosis)", "myofibromatosis caused by mutation in PDGFRB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myofibromatosis, infantile, 1", "shortest_name_length": 3}
{"curie": "UMLS:C2983720", "names": ["Oropharyngeal Carcinoma by AJCC v6 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oropharyngeal Carcinoma by AJCC v6 Stage", "shortest_name_length": 40}
{"curie": "MONDO:0004238", "names": ["Petrous Apex Meningioma", "petrous apex meningioma", "Petrous Ridge Meningioma", "petrous ridge meningioma", "meningioma of petrous apex", "Meningioma of Petrous Apex", "meningioma of petrous ridge", "Meningioma of Petrous Ridge", "meningioma of the petrous apex", "Meningioma of the Petrous Apex", "meningioma of the petrous ridge", "meningioma of the Petrous Ridge", "Meningioma of the Petrous Ridge"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "petrous apex meningioma", "shortest_name_length": 23}
{"curie": "MONDO:0017306", "names": ["disorder of phenylalanine metabolism", "Disorder of phenylalanine metabolism", "DISORDERS OF PHENYLALANINE METABOLISM", "Disorder of phenylalanine metabolism, NOS", "Disorder of phenylalanine metabolism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of phenylalanine metabolism", "shortest_name_length": 36}
{"curie": "UMLS:C5420823", "names": ["Unresectable Lung Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Lung Adenocarcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0023541", "names": ["Kasznica Carlson Coppedge syndrome", "Kasznica-Carlson-Coppedge syndrome", "ectrodactyly spina bifida cardiopathy", "Ectrodactyly spina bifida cardiopathy", "ectrodactyly, retrognathism, abnormal ears, highly arched palate, spina bifida, congenital heart defect, single umbilical artery"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kasznica-Carlson-Coppedge syndrome", "shortest_name_length": 34}
{"curie": "UMLS:C3882647", "names": ["Leukocyte Motility, Abnormal", "Neutrophil Motility, Abnormal", "Neutrophil Migration, Abnormal", "Neutrophil Chemotactic Response, Abnormal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neutrophil Chemotactic Response, Abnormal", "shortest_name_length": 28}
{"curie": "UMLS:C2828185", "names": ["Stage II Gestational Trophoblastic Tumor", "stage II gestational trophoblastic tumor", "Stage II Gestational Trophoblastic Tumor AJCC v7", "stage II gestational trophoblastic tumor AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Gestational Trophoblastic Tumor AJCC v7", "shortest_name_length": 40}
{"curie": "MONDO:0009120", "names": ["marfanoid syndrome, De Silva type", "Marphanoid syndrome type De Silva", "DIVERTICULOSIS OF BOWEL, HERNIA, AND RETINAL DETACHMENT", "Diverticulosis of Bowel, Hernia, and Retinal Detachment", "diverticulosis of bowel, hernia, and retinal detachment"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diverticulosis of bowel, hernia, and retinal detachment", "shortest_name_length": 33}
{"curie": "UMLS:C1514197", "names": ["Polycythemia Vera, Polycythemic Phase", "Polycythemia Vera, Polycythemic Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Polycythemia Vera, Polycythemic Phase", "shortest_name_length": 37}
{"curie": "MONDO:0013471", "names": ["DFNB61", "autosomal recessive deafness 61", "DEAFNESS, AUTOSOMAL RECESSIVE 61", "deafness, autosomal recessive 61", "deafness, autosomal recessive type 61", "autosomal recessive nonsyndromic deafness 61", "autosomal recessive nonsyndromic hearing loss 61", "autosomal recessive nonsyndromic deafness type 61", "SLC26A5 autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic deafness caused by mutation in SLC26A5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 61", "shortest_name_length": 6}
{"curie": "UMLS:C1711278", "names": ["Nasopharyngeal Papillary Adenocarcinoma", "Nasopharyngeal Throat Papillary Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasopharyngeal Papillary Adenocarcinoma", "shortest_name_length": 39}
{"curie": "UMLS:C1540600", "names": ["Apoplectic fit", "Cerebral seizure", "SEIZURE CEREBRAL", "Seizure cerebral", "SEIZURES CEREBRAL", "Seizures cerebral", "Seizure;apoplectic", "apoplectic seizure", "seizure; apoplectic", "Cerebral seizure, NOS", "Apoplectic attack, NOS", "Apoplectic seizure, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebral seizure", "shortest_name_length": 14}
{"curie": "UMLS:C3146253", "names": ["Stage III Rectal Cancer", "Stage III Rectal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Rectal Cancer AJCC v7", "shortest_name_length": 23}
{"curie": "MONDO:0042486", "names": ["HMPS1", "CRCS4", "CRAC1", "Colorectal Adenoma and Carcinoma 1", "colorectal adenoma and carcinoma 1", "COLORECTAL ADENOMA AND CARCINOMA 1", "hereditary mixed polyposis syndrome 1", "polyposis syndrome, hereditary mixed 1", "colorectal cancer, susceptibility to, 4", "Polyposis Syndrome, Hereditary Mixed, 1", "POLYPOSIS SYNDROME, HEREDITARY MIXED, 1", "COLORECTAL CANCER, SUSCEPTIBILITY TO, 4", "polyposis syndrome, hereditary mixed, 1", "chromosome 15Q13-q14 Duplication syndrome, 40-Kb", "CHROMOSOME 15q13-q14 DUPLICATION SYNDROME, 40-KB", "chromosome 15q13-q14 duplication syndrome, 40-KB", "colorectal cancer, susceptibility to, on chromosome 15", "COLORECTAL CANCER, SUSCEPTIBILITY TO, ON CHROMOSOME 15"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyposis syndrome, hereditary mixed, 1", "shortest_name_length": 5}
{"curie": "UMLS:C3272765", "names": ["Appendix High Grade Dysplasia", "Appendiceal High Grade Dysplasia", "Appendix High Grade Intraepithelial Neoplasia", "Appendiceal High Grade Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Appendix High Grade Intraepithelial Neoplasia", "shortest_name_length": 29}
{"curie": "MONDO:0015794", "names": ["Minicore myopathy, antenatal onset, with arthrogryposis", "Multicore myopathy, antenatal onset, with arthrogryposis", "multicore myopathy, antenatal onset, with arthrogryposis", "multiminicore myopathy, antenatal onset, with arthrogryposis", "Multiminicore myopathy, antenatal onset, with arthrogryposis", "antenatal multiminicore disease with arthrogryposis multiplex congenita", "Antenatal multiminicore disease with arthrogryposis multiplex congenita"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "antenatal multiminicore disease with arthrogryposis multiplex congenita", "shortest_name_length": 55}
{"curie": "MONDO:0003693", "names": ["clear cell cystadenofibroma", "Clear cell cystadenofibroma", "Clear Cell Cystadenofibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "clear cell cystadenofibroma", "shortest_name_length": 27}
{"curie": "UMLS:C2347758", "names": ["Grade III Meningioma", "Childhood Grade 3 Meningioma", "grade III childhood meningioma", "childhood grade III meningioma", "Childhood Grade III Meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Grade III Meningioma", "shortest_name_length": 20}
{"curie": "UMLS:C2350622", "names": ["radiation fibrosis", "Radiation Fibrosis", "Radiation fibrosis", "Fibrosis, Radiation", "Radiation Induced Fibrosis", "Radiation-Induced Fibrosis", "fibrosis, radiation-induced", "Radiation Fibrosis Syndrome", "Fibrosis, Radiation-Induced", "Fibrosis Syndrome, Radiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radiation Fibrosis", "shortest_name_length": 18}
{"curie": "UMLS:C0086696", "names": ["Therapy Related Tumor", "Therapy-Related Neoplasm", "Therapy Related Neoplasm", "Therapy Related Neoplasms", "Therapy-Related Neoplasms", "Neoplasm, Therapy-Related", "Neoplasms, Therapy Related", "Treatment-Related Neoplasm", "Neoplasms, Therapy-Related", "Therapy-Associated Neoplasm", "Neoplasm, Treatment-Related", "Treatment-Related Neoplasms", "Treatment Related Neoplasms", "Neoplasm, Therapy-Associated", "Therapy Associated Neoplasms", "Neoplasms, Treatment Related", "Therapy-Associated Neoplasms", "Neoplasms, Treatment-Related", "Neoplasms, Therapy Associated", "Neoplasms, Therapy-Associated", "Treatment-Associated Neoplasm", "Neoplasm, Treatment-Associated", "Treatment Associated Neoplasms", "Treatment-Associated Neoplasms", "Neoplasms, Treatment Associated", "Neoplasms, Treatment-Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplasms, Therapy-Associated", "shortest_name_length": 21}
{"curie": "UMLS:C5670598", "names": ["Recurrent T-Lymphoblastic Lymphoma", "Recurrent T Lymphoblastic Lymphoma", "Recurrent Precursor T-Lymphoblastic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent T Lymphoblastic Lymphoma", "shortest_name_length": 34}
{"curie": "UMLS:C2217040", "names": ["Stage IV Colon Cancer", "Stage IV Colon Cancer AJCC v7", "malignant large intestine neoplasm stage IV", "malignant neoplasm of large intestine stage IV", "malignant large intestine neoplasm stage IV (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant neoplasm of large intestine stage IV", "shortest_name_length": 21}
{"curie": "MONDO:0005556", "names": ["SLE nephritis", "Nephritis SLE", "sle nephritis", "SLE Nephritis", "Lupus nephritis", "nephritis lupus", "lupus nephritis", "LUPUS NEPHRITIS", "Lupus Nephritis", "NEPHRITIS, LUPUS", "nephritis, lupus", "Nephritis, Lupus", "lupus Nephritides", "Lupus Nephritides", "Nephritides, lupus", "Nephritides, Lupus", "Lupus nephritis, NOS", "GLOMERULONEPHRITIS LUPUS", "Lupus Glomerulonephritis", "lupus glomerulonephritis", "Glomerulonephritis, Lupus", "GLOMERULONEPHRITIS, LUPUS", "glomerulonephritis, lupus", "Lupus Glomerulonephritides", "lupus Glomerulonephritides", "Glomerulonephritides, lupus", "Glomerulonephritides, Lupus", "SLE glomerulonephritis syndrome", "SLE glomerulonephritis syndrome, NOS", "Nephritis systemic lupus erythematosus", "nephritis due to systemic lupus erythematosus", "systemic lupus erythematosus glomerulonephritis syndrome", "Systemic lupus erythematosus glomerulonephritis syndrome", "nephritis due to systemic lupus erythematosus (diagnosis)", "Systemic lupus erythematosus glomerulonephritis syndrome (disorder)", "systemic lupus erythematosus glomerulonephritis syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lupus nephritis", "shortest_name_length": 13}
{"curie": "UMLS:C1711263", "names": ["Heart Capillary Hemangioma", "Cardiac Capillary Hemangioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiac Capillary Hemangioma", "shortest_name_length": 26}
{"curie": "UMLS:C0854367", "names": ["Soliloquy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Soliloquy", "shortest_name_length": 9}
{"curie": "MONDO:0013691", "names": ["FS2", "FGLDS2", "MMT type 2", "FEINGOLD SYNDROME 2", "Feingold syndrome 2", "Feingold syndrome type 2", "Brunner-Winter syndrome type 2", "BRACHYDACTYLY WITH SHORT STATURE AND MICROCEPHALY", "brachydactyly-short stature-microcephaly syndrome", "Brachydactyly-short stature-microcephaly syndrome", "brachydactyly with short stature and microcephaly", "microcephaly-digital anomalies-normal intelligence syndrome type 2", "Microcephaly-digital anomalies-normal intelligence syndrome type 2", "microcephaly-intellectual disability-tracheoesophageal fistula syndrome type 2", "Microcephaly-intellectual disability-tracheoesophageal fistula syndrome type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Feingold syndrome type 2", "shortest_name_length": 3}
{"curie": "MONDO:0007172", "names": ["ASD1", "ASD I", "ASD 1", "ASD 2", "ASD II", "atrial septal defect 1", "Atrial Septal Defect 1", "ATRIAL SEPTAL DEFECT 1", "atrial heart septal defect 1", "atrial heart septal defect type 1", "atrial septal defect, primum type", "Atrial septal defect, secundum type", "Atrial Septal Defect, Secundum Type", "ATRIAL SEPTAL DEFECT, SECUNDUM TYPE", "atrial septal defect, secundum type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial septal defect 1", "shortest_name_length": 4}
{"curie": "UMLS:C0341325", "names": ["Anal Leukoplakia", "Anal leukoplakia", "anus; leukoplakia", "leukoplakia; anus", "Leukoplakia of anus", "Leukoplakia of Anus", "Leucoplakia of anus", "Leukoplakia of the Anus", "Leukoplakia of anus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leukoplakia of anus", "shortest_name_length": 16}
{"curie": "MONDO:0023022", "names": ["dwarfism thin bones multiple fractures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dwarfism thin bones multiple fractures", "shortest_name_length": 38}
{"curie": "UMLS:C4054917", "names": ["Functioning PitNET/Macroadenoma", "Functional Pituitary Macroadenoma", "Functioning Pituitary Gland Macroadenoma", "Functioning Pituitary Neuroendocrine Tumor/Macroadenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Functioning Pituitary Neuroendocrine Tumor/Macroadenoma", "shortest_name_length": 31}
{"curie": "UMLS:C0270148", "names": ["attack; cyanotic, newborn", "Perinatal Cyanotic Attack", "Perinatal cyanotic attacks", "cyanotic attacks of newborn", "Cyanotic attacks of newborn", "Perinatal cyanotic attacks, NOS", "Perinatal cyanotic attacks (finding)", "cyanotic attacks of newborn (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Perinatal cyanotic attacks", "shortest_name_length": 25}
{"curie": "UMLS:C0406143", "names": ["listeriosis cutaneous", "Cutaneous listeriosis", "listeriosis; cutaneous", "cutaneous; listeriosis", "Cutaneous listeriosis (disorder)", "listeriosis cutaneous (diagnosis)", "Cutaneous involvement in listeriosis", "Cutaneous involvement by listeriosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous listeriosis", "shortest_name_length": 21}
{"curie": "MONDO:0012503", "names": ["TPMTD", "THPM1", "TPMT deficiency", "TPMT DEFICIENCY", "TPMT Deficiency", "6-mercaptopurine sensitivity", "Thiopurines, poor metabolism of", "poor metabolism of thiopurines-1", "thiopurines, poor metabolism of, 1", "THIOPURINES, POOR METABOLISM OF, 1", "Thiopurines, poor metabolism of, 1", "Thiopurine Methyltransferase Deficiency", "Thiopurine methyltransferase deficiency", "thiopurine methyltransferase deficiency", "Thiopurine S methyltranferase deficiency", "thiopurine S methyltranferase deficiency", "Thiopurine S-Methyltransferase Deficiency", "THIOPURINE S-METHYLTRANSFERASE DEFICIENCY", "thiopurine S-methyltransferase deficiency", "TPMT - Thiopurine methyltransferase deficiency", "Thiopurine methyltransferase deficiency (diagnosis)", "inborn error of thiopurine S-methyltransferase activity", "inborn thiopurine S-methyltransferase activity disorder", "rare inborn error of thiopurine S-methyltransferase activity", "disorder purine & pyrimidine metabolism thiopurine methyltransferase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thiopurine S-methyltransferase deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C4525141", "names": ["Stage IV Rectal Cancer", "Stage IV Rectal Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Rectal Cancer AJCC v8", "shortest_name_length": 22}
{"curie": "UMLS:C1336872", "names": ["Upper Gum Verrucous Carcinoma", "Verrucous Carcinoma of Upper Gum", "Upper Gingival Verrucous Carcinoma", "Verrucous Carcinoma of the Upper Gum", "Verrucous Carcinoma of Upper Gingiva", "Verrucous Carcinoma of the Upper Gingiva"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Upper Gingival Verrucous Carcinoma", "shortest_name_length": 29}
{"curie": "UMLS:C1402865", "names": ["Liver Teratoma", "teratoma; liver", "liver; teratoma", "Hepatic Teratoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liver Teratoma", "shortest_name_length": 14}
{"curie": "MONDO:0700107", "names": ["CHROMOSOME 19q13.11 DELETION SYNDROME, DISTAL", "chromosome 19q13.11 deletion syndrome, distal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 19q13.11 deletion syndrome, distal", "shortest_name_length": 45}
{"curie": "MONDO:0003878", "names": ["melanoma choroid", "Choroid Melanoma", "Choroid melanoma", "choroid melanoma", "choroid; melanoma", "melanoma; choroid", "Choroidal melanoma", "choroidal melanoma", "Choroidal Melanoma", "melanoma of choroid", "Melanoma of choroid", "Melanoma of Choroid", "optic choroid melanoma", "melanoma of the choroid", "melanoma of the Choroid", "Melanoma of the Choroid", "Choroid Malignant Melanoma", "malignant choroid melanoma", "choroid malignant melanoma", "Malignant melanoma of choroid", "malignant melanoma of choroid", "Malignant Melanoma of Choroid", "optic choroid melanoma (disease)", "malignant melanoma of the choroid", "Malignant Melanoma of the Choroid", "melanoma (disease) of optic choroid", "Malignant melanoma of choroid (disorder)", "malignant melanoma of choroid (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant choroid melanoma", "shortest_name_length": 16}
{"curie": "MONDO:0011887", "names": ["cataract, congenital, with mental impairment and dentate gyrus atrophy", "CATARACT, CONGENITAL, WITH MENTAL IMPAIRMENT AND DENTATE GYRUS ATROPHY", "Cataract, Congenital, with Mental Impairment and Dentate Gyrus Atrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract, congenital, with mental impairment and dentate gyrus atrophy", "shortest_name_length": 70}
{"curie": "MONDO:0012291", "names": ["IGAD2", "immunoglobulin a deficiency 2", "Immunoglobulin a deficiency 2", "IMMUNOGLOBULIN A deficiency 2", "IMMUNOGLOBULIN A DEFICIENCY 2", "immunoglobulin A deficiency 2", "Immunoglobulin a deficiency type 2", "IgA, selective deficiency of, TACI-related", "TNFRSF13B selective IgA deficiency disease", "IgA, selective deficiency of, TACI related", "Iga, selective deficiency of, taci-related", "IgA, SELECTIVE DEFICIENCY OF, TACI-RELATED", "Immunoglobulin A, selective deficiency of, TACI related", "Immunoglobulin a, selective deficiency of, taci-related", "IMMUNOGLOBULIN A, SELECTIVE DEFICIENCY OF, TACI-RELATED", "Immunoglobulin A, selective deficiency of, TACI-related", "selective IgA deficiency disease caused by mutation in TNFRSF13B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunoglobulin A deficiency 2", "shortest_name_length": 5}
{"curie": "UMLS:C4054325", "names": ["Obesity Related Glomerulopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Obesity Related Glomerulopathy", "shortest_name_length": 30}
{"curie": "MONDO:0012057", "names": ["Legionella infection", "legionnaire's disease", "susceptibility to legionnaire disease", "legionnaire disease, susceptibility to", "LEGIONNAIRE DISEASE, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "legionnaire disease, susceptibility to", "shortest_name_length": 20}
{"curie": "MONDO:0007444", "names": ["dermal Ridges, patternless", "Dermal Ridges, Patternless", "DERMAL RIDGES, PATTERNLESS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermal Ridges, patternless", "shortest_name_length": 26}
{"curie": "MONDO:0032749", "names": ["DFNB94", "autosomal recessive deafness 94", "deafness, autosomal recessive 94", "DEAFNESS, AUTOSOMAL RECESSIVE 94", "hearing loss, autosomal recessive 94", "autosomal recessive nonsyndromic deafness 94"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal recessive 94", "shortest_name_length": 6}
{"curie": "MONDO:0015821", "names": ["mycosis fungoides and variants"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mycosis fungoides and variants", "shortest_name_length": 30}
{"curie": "MONDO:0033006", "names": ["GAMOS2", "Galloway-Mowat syndrome 2", "GALLOWAY-MOWAT SYNDROME 2, X-LINKED", "Galloway-Mowat syndrome 2, X-linked", "Galloway-Mowat syndrome 2, X-linked, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Galloway-Mowat syndrome 2, X-linked", "shortest_name_length": 6}
{"curie": "MONDO:0030476", "names": ["GAMOS10", "Galloway-Mowat syndrome 10", "GALLOWAY-MOWAT SYNDROME 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Galloway-Mowat syndrome 10", "shortest_name_length": 7}
{"curie": "MONDO:0018009", "names": ["non-hypoproteinemic hypertrophic gastropathy", "hypertrophic gastropathy without hypoproteinemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-hypoproteinemic hypertrophic gastropathy", "shortest_name_length": 44}
{"curie": "UMLS:C4763788", "names": ["Refractory Plasmablastic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Plasmablastic Lymphoma", "shortest_name_length": 33}
{"curie": "MONDO:0017752", "names": ["defect in V-ATPase"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "defect in V-ATPase", "shortest_name_length": 18}
{"curie": "MONDO:0017450", "names": ["split foot", "Split feet", "Cleft foot", "Split-foot", "Split foot", "foot; cleft", "cleft; foot", "Lobster claw foot", "Foot ectrodactyly", "lobster claw foot", "split foot (disease)", "Ectrodactyly of feet", "Split foot (disorder)", "split foot (diagnosis)", "Lobster-claw foot deformity", "congenital deformity split foot", "Split foot, unspecified lower limb"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "split foot", "shortest_name_length": 10}
{"curie": "MONDO:0007389", "names": ["TACS", "SCDO5", "polydysspondyly", "SPONDYLOCOSTAL DYSPLASIA", "spondylocostal dysplasia", "spondylothoracic dysostosis", "SPONDYLOTHORACIC DYSOSTOSIS", "SPONDYLOCOSTAL DYSOSTOSIS 5", "spondylocostal dysostosis 5", "TBX6 spondylocostal dysostosis", "spondylocostal dysostosis type 5", "costovertebral segmentation anomalies", "COSTOVERTEBRAL SEGMENTATION ANOMALIES", "SCOLIOSIS, CONGENITAL, WITH OR WITHOUT RIB ANOMALIES", "scoliosis, congenital, with or without rib anomalies", "spondylocostal dysostosis caused by mutation in TBX6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondylocostal dysostosis 5", "shortest_name_length": 4}
{"curie": "MONDO:0008647", "names": ["ASH", "ash", "Cmh", "CMH1", "IHSS", "ihss", "ihsss", "Asymmetric Septal Hypertrophy", "hypertrophic cardiomyopathy 1", "Asymmetric septal hypertrophy", "asymmetric septal Hypertrophy", "ASYMMETRIC SEPTAL HYPERTROPHY", "asymmetric septal hypertrophy", "hypertrophic cardiomyopathy 19", "HYPERTROPHIC SUBAORTIC STENOSIS", "Hypertrophic subaortic stenosis", "hypertrophic subaortic stenosis", "MYH7 hypertrophic cardiomyopathy", "stenosis; subaortic, hypertrophic", "Hereditary Ventricular Hypertrophy", "hypertrophic cardiomyopathy type 1", "ventricular Hypertrophy, hereditary", "asymmetric septal hypertrophy (ASH)", "asymmetric cardiac septal hypertrophy", "cardiomyopathy, familial hypertrophic 1", "cardiomyopathy, familial hypertrophic, 1", "CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 1", "Cardiomyopathy, Familial Hypertrophic, 1", "idiopathic hypertrophic subaortic stenosis", "Idiopathic hypertrophic subaortic stenosis", "IDIOPATHIC HYPERTROPHIC SUBAORTIC STENOSIS", "Idiopathic Hypertrophic Subaortic Stenosis", "Familial Hypertrophic Cardiomyopathy Type 1", "hypertrophic subaortic stenosis, idiopathic", "HYPERTROPHIC SUBAORTIC STENOSIS, IDIOPATHIC", "Hypertrophic Subaortic Stenosis, Idiopathic", "Hypertrophic subaortic stenosis (idiopathic)", "cardiomyopathy, familial hypertrophic, type 1", "idiopathic hypertrophic subaortic stenosis (IHSS)", "IHSS (idiopathic hypertrophic subaortic stenosis)", "asymmetric cardiac septal hypertrophy (diagnosis)", "hypertrophic cardiomyopathy caused by mutation in MYH7", "idiopathic hypertrophic subaortic stenosis (diagnosis)", "cardiomyopathy, hypertrophic, 1, Autosomal dominant, Digenic dominant", "cardiomyopathy, familial hypertrophic, Autosomal dominant, Digenic dominant", "cardiomyopathy, hypertrophic, 1, digenic, Autosomal dominant, Digenic dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophic cardiomyopathy 1", "shortest_name_length": 3}
{"curie": "MONDO:0800143", "names": ["cytomegalovirus pneumonia due to NOS2 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cytomegalovirus pneumonia due to NOS2 deficiency", "shortest_name_length": 48}
{"curie": "MONDO:0009274", "names": ["GHDD", "Ghosal syndrome", "Ghosal Syndrome", "GHOSAL SYNDROME", "Ghosal hematodiaphyseal syndrome", "Diaphyseal dysplasia with anemia", "Ghosal hematodiaphyseal dysplasia", "GHOSAL hematodiaphyseal dysplasia", "GHOSAL HEMATODIAPHYSEAL DYSPLASIA", "Diaphyseal dysplasia with anaemia", "Ghosal Hematodiaphyseal Dysplasia", "ghosal hematodiaphyseal dysplasia", "Ghosal haematodiaphyseal dysplasia", "Diaphyseal dysplasia-anemia syndrome", "diaphyseal dysplasia-anemia syndrome", "Diaphyseal dysplasia anemia syndrome", "Diaphyseal dysplasia anaemia syndrome", "Ghosal hematodiaphyseal dysplasia syndrome", "Ghosal hematodiaphyseal dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ghosal hematodiaphyseal dysplasia", "shortest_name_length": 4}
{"curie": "UMLS:C5419624", "names": ["Severe ARDS", "Severe Acute Respiratory Distress Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Severe Acute Respiratory Distress Syndrome", "shortest_name_length": 11}
{"curie": "UMLS:C5555500", "names": ["Platinum-Resistant Head and Neck Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Platinum-Resistant Head and Neck Carcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0015542", "names": ["reactive hemophagocytic syndrome", "acquired hemophagocytic syndrome", "Reactive hemophagocytic syndrome", "Reactive Hemophagocytic Syndrome", "Hemophagocytic Syndrome, Reactive", "Reactive haemophagocytic syndrome", "Hemophagocytic syndrome due to infection", "Haemophagocytic syndrome due to infection", "acquired hemophagocytic lymphohistiocytosis", "Acquired hemophagocytic lymphohistiocytosis", "Infection-associated hemophagocytic syndrome", "infection-associated hemophagocytic syndrome", "Infection-Associated Hemophagocytic Syndrome", "Secondary Hemophagocytic Lymphohistiocytosis", "Secondary hemophagocytic lymphohistiocytosis", "secondary hemophagocytic lymphohistiocytosis", "Hemophagocytic Syndrome, Infection-Associated", "Secondary haemophagocytic lymphohistiocytosis", "Infection-associated haemophagocytic syndrome", "Hemophagocytic syndrome, infection-associated", "Hemophagocytic Syndrome, Infection Associated", "Infection-induced hemophagocytic histiocytosis", "Haemophagocytic syndrome, infection-associated", "Infection-induced haemophagocytic histiocytosis", "Hemophagocytic lymphohistiocytosis due to infection", "Haemophagocytic lymphohistiocytosis due to infection", "Secondary hemophagocytic lymphohistiocytosis (disorder)", "infection-associated hemophagocytic syndrome (diagnosis)", "Hemophagocytic lymphohistiocytosis due to infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary hemophagocytic lymphohistiocytosis", "shortest_name_length": 32}
{"curie": "UMLS:C3274494", "names": ["Ileal Web"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ileal Web", "shortest_name_length": 9}
{"curie": "MONDO:0016703", "names": ["aMOA", "AOAST", "Anaplastic Mixed Glioma", "anaplastic mixed glioma", "WHO Grade 3 Mixed Glioma", "WHO grade III mixed glioma", "WHO Grade III Mixed Glioma", "Anaplastic Oligoastrocytoma", "anaplastic oligoastrocytoma", "Anaplastic oligoastrocytoma", "Anaplastic Oligoastrocytoma, NOS", "Anaplastic Oligoastrocytoma, Not Otherwise Specified", "Anaplastic oligoastrocytoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anaplastic oligoastrocytoma", "shortest_name_length": 4}
{"curie": "MONDO:0008751", "names": ["FHHA1A", "CMO I Deficiency", "CMO 1 deficiency", "CMO I DEFICIENCY", "CMO I deficiency", "CMO II Deficiency", "CMO II deficiency", "18-Oxidase Deficiency", "aldosterone deficiency 1", "ALDOSTERONE DEFICIENCY I", "Aldosterone deficiency 1", "18-Hydroxylase deficiency", "18-HYDROXYLASE DEFICIENCY", "18 Hydroxylase deficiency", "18-hydroxylase deficiency", "Aldosterone Deficiency Type I", "Steroid 18-Oxidase Deficiency", "Aldosterone Deficiency Type II", "CAH - 18-hydroxylase deficiency", "aldosterone synthase deficiency", "18 alpha hydroxylase deficiency", "18-alpha hydroxylase deficiency", "steroid 18-hydroxylase deficiency", "STEROID 18-HYDROXYLASE DEFICIENCY", "Steroid 18-Hydroxylase Deficiency", "18-hydroxylase deficiency (diagnosis)", "corticosterone methyloxidase deficiency 1", "corticosterone 18-monooxygenase deficiency", "Corticosterone 18-monooxygenase deficiency", "hyperreninemic hypoaldosteronism, familial, 1", "HYPERRENINEMIC HYPOALDOSTERONISM, FAMILIAL, 1", "corticosterone methyloxidase type 1 deficiency", "Corticosterone methyloxidase type 1 deficiency", "corticosterone methyloxidase type I deficiency", "CORTICOSTERONE METHYLOXIDASE TYPE I DEFICIENCY", "Corticosterone Methyloxidase Type I Deficiency", "corticosterone methyl oxidase type I deficiency", "Corticosterone Methyloxidase Type II Deficiency", "Corticosterone methyl oxidase type I deficiency", "Corticosterone Methyl Oxidase Type I Deficiency", "corticosterone methyl oxidase type II deficiency", "18-hydroxycorticosterone dehydrogenase deficiency", "18-Hydroxycorticosterone dehydrogenase deficiency", "Hyperreninemic Hypoaldosteronism, Familial, Type I", "aldosterone deficiency due to 18-hydroxylase defect", "Aldosterone deficiency due to 18-hydroxylase defect", "Corticosterone 18-monooxygenase deficiency (disorder)", "aldosterone deficiency due to defect in 18 hydroxylase", "hypoaldosteronism, congenital, due to cmo i deficiency", "Aldosterone deficiency due to defect in 18-hydroxylase", "aldosterone deficiency due to defect in steroid 18-Hydroxylase", "ALDOSTERONE DEFICIENCY DUE TO DEFECT IN STEROID 18-HYDROXYLASE", "Aldosterone deficiency due to 18-hydroxysteroid dehydrogenase deficiency", "aldosterone deficiency due to 18-hydroxysteroid dehydrogenase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corticosterone methyloxidase type 1 deficiency", "shortest_name_length": 6}
{"curie": "MONDO:0000681", "names": ["tactile agnosia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tactile agnosia", "shortest_name_length": 15}
{"curie": "UMLS:C4524744", "names": ["Postneoadjuvant Therapy Stage I Gastroesophageal Junction Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postneoadjuvant Therapy Stage I Gastroesophageal Junction Adenocarcinoma AJCC v8", "shortest_name_length": 80}
{"curie": "UMLS:C4683654", "names": ["T-Cell Non-Hodgkin Lymphoma by Ann Arbor Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-Cell Non-Hodgkin Lymphoma by Ann Arbor Stage", "shortest_name_length": 46}
{"curie": "MONDO:0006412", "names": ["RDD", "SHML", "Sinus Histiocytosis", "histiocytosis sinus", "Sinus Histiocytoses", "sinus histiocytosis", "Sinus histiocytosis", "sinus; histiocytosis", "Histiocytosis, sinus", "Histiocytoses, Sinus", "Histiocytosis, Sinus", "histiocytosis; sinus", "Rosai-Dorfman Disease", "Rosai Dorfman Disease", "Rosaï-Dorfman disease", "Rosai-Dorfman disease", "rosai-dorfman disease", "rosai dorfman disease", "disease rosai-dorfman", "Rosai-Dorfman syndrome", "Disease, Rosai-Dorfman", "Rosaï-Dorfman-Destombes disease", "Destombes-Rosaï-Dorfman disease", "Destombes Rosai Dorfman Syndrome", "Destombes-RosaC/-Dorfman disease", "Destombes-Rosai-Dorfman Syndrome", "destombes-rosai-dorfman syndrome", "RosaC/-Dorfman-Destombes disease", "Syndrome, Destombes-Rosai-Dorfman", "Sinus histiocytosis (morphologic abnormality)", "sinus histiocytosis with massive lymphadenopathy", "Sinus histiocytosis with massive lymphadenopathy", "Sinus Histiocytosis with Massive Lymphadenopathy", "Sinus histiocytosis with massive lymphadenopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sinus histiocytosis with massive lymphadenopathy", "shortest_name_length": 3}
{"curie": "UMLS:C1333305", "names": ["Disease by Site", "Disorder by Site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disorder by Site", "shortest_name_length": 15}
{"curie": "MONDO:0100315", "names": ["isolated adrenal insufficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated adrenal insufficiency", "shortest_name_length": 30}
{"curie": "MONDO:0011217", "names": ["DESMOSTEROLOSIS", "desmosterolosis", "Desmosterolosis", "Desmosterolosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "desmosterolosis", "shortest_name_length": 15}
{"curie": "MONDO:0011506", "names": ["Eim", "EIM", "FIME", "Infantile Myoclonic Epilepsy", "Myoclonic Epilepsy, Infantile", "Epilepsy, Infantile Myoclonic", "Infantile Myoclonic Epilepsies", "Epilepsy, Myoclonic, Infantile", "Epilepsies, Infantile Myoclonic", "Myoclonic Epilepsies, Infantile", "Familial infantile myoclonic epilepsy", "familial infantile myoclonus epilepsy", "Familial infantile myoclonus epilepsy", "familial infantile myoclonic epilepsy", "MYOCLONIC EPILEPSY, FAMILIAL INFANTILE", "myoclonic epilepsy, familial infantile", "myoclonic epilepsy, infantile, familial", "MYOCLONIC EPILEPSY, INFANTILE, FAMILIAL", "FIME - familial infantile myoclonic epilepsy", "Familial infantile myoclonic epilepsy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial infantile myoclonic epilepsy", "shortest_name_length": 3}
{"curie": "MONDO:0016794", "names": ["maternally-inherited mitochondrial myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maternally-inherited mitochondrial myopathy", "shortest_name_length": 43}
{"curie": "MONDO:0014372", "names": ["CORD19", "CONE-ROD DYSTROPHY 19", "cone-rod dystrophy 19", "TTLL5 cone-rod dystrophy", "cone-rod dystrophy type 19", "cone-rod dystrophy caused by mutation in TTLL5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cone-rod dystrophy 19", "shortest_name_length": 6}
{"curie": "UMLS:C1335484", "names": ["Primary Gastric T-Cell Lymphoma", "Primary T-Cell Lymphoma of Stomach", "Gastric T-Cell Non-Hodgkin Lymphoma", "Gastric T-Cell Non-Hodgkin's Lymphoma", "Primary T-Cell Lymphoma of the Stomach", "Primary Gastric T-Cell Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric T-Cell Non-Hodgkin Lymphoma", "shortest_name_length": 31}
{"curie": "MONDO:0022873", "names": ["corpus callosum dysgenesis cleft spasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corpus callosum dysgenesis cleft spasm", "shortest_name_length": 38}
{"curie": "MONDO:0017581", "names": ["familial infantile gigantism", "hereditary infantile gigantism", "X-LAG (X-linked acrogigantism)", "hereditary pituitary hyperplasia", "infantile gigantism due to pituitary hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial infantile gigantism", "shortest_name_length": 28}
{"curie": "MONDO:0004919", "names": ["Pyocele", "Pycocele", "Infected hydrocele", "infected hydrocele", "hydrocele; infected", "infected; hydrocele", "Hydrocele male infected", "Infected hydrocele (disorder)", "infected hydrocele (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infected hydrocele", "shortest_name_length": 7}
{"curie": "MONDO:0013467", "names": ["LCAPD3", "Fcn3 deficiency", "FCN3 DEFICIENCY", "ficolin 3 deficiency", "FICOLIN 3 DEFICIENCY", "immunodeficiency due to ficolin3 deficiency", "immunodeficiency due to ficolin 3 deficiency", "Immunodeficiency due to ficolin 3 deficiency", "Immunodeficiency due to ficolin-3 deficiency", "LECTIN COMPLEMENT ACTIVATION PATHWAY, DEFECT IN, 3", "lectin complement activation pathway, defect in, 3", "Immunodeficiency due to ficolin 3 deficiency (disorder)", "immunodeficiency due to ficolin 3 deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency due to ficolin3 deficiency", "shortest_name_length": 6}
{"curie": "MONDO:0017768", "names": ["reflex epilepsy", "epilepsy reflex", "Reflex epilepsy", "Reflex Epilepsy", "Epilepsy, Reflex", "epilepsy; reflex", "Reflex Epilepsies", "Epilepsies, Reflex", "Sensory-induced epilepsy", "epilepsy, sensory-induced", "Epilepsy, sensory-induced", "Reflex epilepsy (disorder)", "Reflex epilepsy (diagnosis)", "Epilepsy associated with specific stimuli"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "reflex epilepsy", "shortest_name_length": 15}
{"curie": "UMLS:C1832612", "names": ["Hypocalcemia, Autosomal Dominant, with Bartter Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypocalcemia, Autosomal Dominant, with Bartter Syndrome", "shortest_name_length": 55}
{"curie": "MONDO:0001256", "names": ["AVM", "AVM/H", "av malformation", "AV MALFORMATION", "Aneurysmal varix", "Cirsoid aneurysm", "a v malformation", "Racemose Angioma", "A-V malformation", "cirsoid aneurysm", "a-v malformation", "av malformations", "Racemose angioma", "racemose angioma", "a v malformations", "aneurysmal; varix", "racemose aneurysm", "Racemose aneurysm", "varix; aneurysmal", "aneurysm; racemose", "racemose; aneurysm", "Racemose Hemangioma", "Arterial hemangioma", "racemose hemangioma", "Racemose hemangioma", "Hemangioma arterial", "arterial hemangioma", "Racemose haemangioma", "Haemangioma arterial", "hemangioma; racemose", "racemose; hemangioma", "arteriovenous angioma", "Arteriovenous anomaly", "Arteriovenous Angioma", "arteriovenous anomaly", "anomalies arteriovenous", "arteriovenous; deformity", "Venous racemose aneurysm", "Arteriovenous hemangioma", "deformity; arteriovenous", "Diffuse arterial ectasia", "Arteriovenous Hemangioma", "arteriovenous hemangioma", "Arteriovenous haemangioma", "arteriovenous haemangioma", "hemangioma; arteriovenous", "arteriovenous; hemangioma", "Arteriovenous Malformation", "Arteriovenous malformation", "arteriovenous malformation", "Cirsoid aneurysm (disorder)", "arteriovenous malformations", "Malformation, Arteriovenous", "Arteriovenous Malformations", "Arteriovenous malformations", "Malformations, Arteriovenous", "Arteriovenous malformation, NOS", "Arteriovenous hemangioma (disorder)", "CONGENITAL ARTERIOVENOUS MALFORMATION", "arteriovenous hemangioma/malformation", "Arteriovenous Malformation/Hemangioma", "Arteriovenous Hemangioma/Malformation", "Congenital arteriovenous malformation", "AV - Congenital arteriovenous anomaly", "arteriovenous malformation (diagnosis)", "Arteriovenous Malformation, Unspecified", "AV - Congenital arteriovenous malformation", "AVM - Congenital arteriovenous malformation", "Racemose aneurysm (morphologic abnormality)", "racemose aneurysm (morphologic abnormality)", "Racemose hemangioma (morphologic abnormality)", "racemose hemangioma (morphologic abnormality)", "Congenital arteriovenous malformation (disorder)", "Arteriovenous malformation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arteriovenous hemangioma/malformation", "shortest_name_length": 3}
{"curie": "UMLS:C5206780", "names": ["Recurrent Malignant Myoepithelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Malignant Myoepithelioma", "shortest_name_length": 34}
{"curie": "MONDO:0002316", "names": ["HSMN", "Motor Neuropathy", "Motor polyneuropathy", "Motor Polyneuropathy", "motor polyneuropathy", "Polyneuropathy, Motor", "Motor Polyneuropathies", "Polyneuropathies, Motor", "motor peripheral neuropathy", "peripheral motor neuropathy", "Peripheral motor neuropathy", "Peripheral Motor Neuropathy", "neuropathic muscular atrophy", "Motor polyneuropathy (disorder)", "hereditary motor and sensory neuropathy", "Hereditary motor and sensory neuropathy", "HSMN - Hereditary sensory and motor neuropathy", "HSMN - hereditary sensory and motor neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "motor peripheral neuropathy", "shortest_name_length": 4}
{"curie": "MONDO:0014516", "names": ["MCCRP2", "microcephaly and chorioretinopathy 2", "PLK4 microcephaly and chorioretinopathy", "microcephaly and chorioretinopathy type 2", "microcephaly and chorioretinopathy, autosomal recessive, 2", "MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 2", "microcephaly and chorioretinopathy caused by mutation in PLK4", "microcephaly and chorioretinopathy, autosomal recessive, type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly and chorioretinopathy 2", "shortest_name_length": 6}
{"curie": "UMLS:C0278056", "names": ["abnormal pregnancy", "Abnormal pregnancy", "Abnormal Pregnancy", "pregnancy abnormal", "pregnancy; abnormal", "abnormal; pregnancy", "Pregnancy, abnormal", "Abnormal pregnancy, NOS", "Abnormal pregnancy (finding)", "finding of abnormal pregnancy", "clinical finding pregnancy abnormal", "finding of abnormal pregnancy (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abnormal pregnancy", "shortest_name_length": 18}
{"curie": "UMLS:C0278567", "names": ["Mycosis fungoides stage I", "Stage I Mycosis Fungoides", "Mycosis Fungoides Stage I", "Stage I Mycosis Fungoides AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mycosis fungoides stage I", "shortest_name_length": 25}
{"curie": "UMLS:C0010709", "names": ["Cyst", "cyst", "CYST", "CYSTS", "cysts", "Cysts", "Cyst(s)", "CYST NOS", "Cyst NOS", "Cyst, NOS", "Cyst (disorder)", "Cyst (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cyst", "shortest_name_length": 4}
{"curie": "MONDO:0003598", "names": ["Median neuropathy", "median neuropathy", "Median Neuropathy", "nerve palsy median", "median nerve palsy", "Neuropathy, Median", "Median nerve palsy", "Median nerve lesion", "median nerve lesion", "Median Neuropathies", "lesions median nerve", "Median Nerve Disease", "Nerve Disease, Median", "Median Mononeuropathy", "Median Nerve Diseases", "Mononeuropathy, Median", "Median Nerve Neuropathy", "Median Mononeuropathies", "median nerve neuropathy", "Nerve Neuropathy, Median", "Neuropathy, Median Nerve", "Median Nerve Neuropathies", "Median neuropathy (disorder)", "Other lesion of median nerve", "Other lesions of median nerve", "median nerve palsy (diagnosis)", "median nerve peripheral neuropathy", "disease (or disorder); median nerve", "peripheral neuropathy of median nerve", "Other lesions of median nerve, unspecified upper limb"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "median nerve neuropathy", "shortest_name_length": 17}
{"curie": "MONDO:0011967", "names": ["PVNH3", "PERIVENTRICULAR NODULAR HETEROTOPIA 3", "periventricular nodular heterotopia 3", "Periventricular Nodular Heterotopia 3", "HETEROTOPIA, PERIVENTRICULAR, ASSOCIATED WITH CHROMOSOME 5p ANOMALIES", "Heterotopia, Periventricular, associated with Chromosome 5p Anomalies", "heterotopia, periventricular, associated with chromosome 5P anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heterotopia, periventricular, associated with chromosome 5P anomalies", "shortest_name_length": 5}
{"curie": "MONDO:0012325", "names": ["Nguyen syndrome", "NGUYEN SYNDROME", "MCA/MR WITH HYPOCHOLESTEROLEMIA DUE TO FAMILIAL HYPOBETALIPOPROTEINEMIA", "MCA/Mr with hypocholesterolemia due to familial hypobetalipoproteinemia", "MCA/MR syndrome with hypocholesterolemia due to familial hypobetalipoproteinemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nguyen syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0013352", "names": ["FOXP1 syndrome", "MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES", "intellectual disability-severe speech delay-mild dysmorphism syndrome", "Mental retardation with language impairment and with or without autistic features", "MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES", "mental retardation with language impairment and with or without autistic features", "FOXP1 related global developmental delay, intellectual disability and speech defects", "intellectual disability with language impairment and with or without autistic features", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability-severe speech delay-mild dysmorphism syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C5237751", "names": ["Localized Esophageal Carcinoma", "Non-Metastatic Esophageal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized Esophageal Carcinoma", "shortest_name_length": 30}
{"curie": "UMLS:C4075565", "names": ["Fifth nerve palsy", "Cranial nerve palsy V", "Cranial Nerve V Palsy", "Cranial nerve 5 palsy", "Trigeminal nerve palsy", "Trigeminal Nerve Palsy", "Fifth Cranial Nerve Palsy", "Trigeminal nerve palsy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Trigeminal nerve palsy", "shortest_name_length": 17}
{"curie": "MONDO:0060578", "names": ["NEMMLAS", "Mitochondrial tryptophanyl-tRNA synthetase deficiency", "WARS2-related combined oxidative phosphorylation defect", "Tryptophanyl tRNA synthetase 2, mitochondrial-related combined oxidative phosphorylation defect", "Tryptophanyl tRNA synthetase 2, mitochondrial-related combined oxidative phosphorylation defect (disorder)", "NEURODEVELOPMENTAL DISORDER, MITOCHONDRIAL, WITH ABNORMAL MOVEMENTS AND LACTIC ACIDOSIS, WITH OR WITHOUT SEIZURES", "neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures", "shortest_name_length": 7}
{"curie": "UMLS:C5557355", "names": ["Endometrial MALT Lymphoma", "Endometrial Mucosa-Associated Lymphoid Tissue Lymphoma", "Endometrial Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endometrial Mucosa-Associated Lymphoid Tissue Lymphoma", "shortest_name_length": 25}
{"curie": "MONDO:0009061", "names": ["CF", "MUCOVISCIDOSIS", "mucoviscidosis", "Mucoviscidosis", "CYSTIC FIBROSIS", "Cystic Fibrosis", "cystic fibrosis", "Cystic fibrosis", "Fibrosis, Cystic", "cystic; fibrosis", "fibrosis; cystic", "disease fibrocystic", "fibrocystic disease", "Cystic fibrosis NOS", "Disease;fibrocystic", "Fibrocystic disease", "disease; fibrocystic", "fibrocystic; disease", "diseases fibrocystic", "cystic fibrosis (CF)", "CF (cystic fibrosis)", "CF - Cystic fibrosis", "cystic disorder fibrosis", "pancreas cystic fibrosis", "cystic fibrosis pancreas", "Cystic fibrosis (disorder)", "cystic fibrosis (diagnosis)", "Cystic fibrosis, unspecified", "disease fibrocystic pancreas", "fibrocystic disease of pancreas", "cystic fibrosis lung disease, modifier of", "pseudomonas aeruginosa, susceptibility to chronic infection by, in cystic fibrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cystic fibrosis", "shortest_name_length": 2}
{"curie": "MONDO:0054782", "names": ["HLD15", "hypomyelinating leukodystrophy 15", "LEUKODYSTROPHY, HYPOMYELINATING, 15", "leukodystrophy, hypomyelinating, 15"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukodystrophy, hypomyelinating, 15", "shortest_name_length": 5}
{"curie": "MONDO:0016581", "names": ["CAFS", "CTHM", "Aortic arch obstruction", "interrupted aortic arch", "Interrupted aortic arch", "INTERRUPTED AORTIC ARCH", "interrupted aortic Arch", "Interrupted Aortic Arch", "aortic arch interruption", "Aortic arch interruption", "an interrupted aortic arch", "Obstruction of aortic arch", "obstruction of aortic arch", "conotruncal cardiac defects", "truncus arteriosus communis", "Conotruncal cardiac defects", "Interruption of aortic arch", "IAA - Interrupted aortic arch", "persistent truncus arteriosus", "Double-outlet right ventricle", "Atretic transverse aortic arch", "conotruncal heart malformations", "Taussig-Bing syndrome or defect", "Conotruncal heart malformations", "CONOTRUNCAL HEART MALFORMATIONS", "Conotruncal Anomaly Face Syndrome", "CONOTRUNCAL ANOMALY FACE SYNDROME", "conotruncal anomaly face syndrome", "Interrupted aortic arch (disorder)", "interrupted aortic arch (diagnosis)", "Obstruction of aortic arch (disorder)", "obstruction of aortic arch (diagnosis)", "conotruncal anomaly face syndrome (CTAF)", "Conotruncal Anomaly Face Syndrome (CTAF)", "conotruncal heart malformations, variable", "CONOTRUNCAL HEART MALFORMATIONS (disorder)", "CONOTRUNCAL ANOMALY FACE SYNDROME/VELOCARDIOFACIAL SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "conotruncal heart malformations", "shortest_name_length": 4}
{"curie": "MONDO:0007735", "names": ["congenital Horner syndrome", "Congenital Horner syndrome", "HORNER SYNDROME, CONGENITAL", "HORNER syndrome, congenital", "Horner Syndrome, Congenital", "Congenital Horner's syndrome", "congenital Horner syndrome (disease)", "Congenital Horner syndrome (disorder)", "congenital Claude-Bernard-Horner syndrome", "Congenital Claude Bernard Horner syndrome", "Congenital Claude-Bernard-Horner syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital Horner syndrome", "shortest_name_length": 26}
{"curie": "MONDO:0010262", "names": ["Hypotonia, congenital nystagmus, ataxia and abnormal auditory brainstem response", "hypotonia, congenital nystagmus, ataxia and abnormal auditory brainstem response", "Hypotonia, Congenital Nystagmus, Ataxia, And Abnormal Auditory Brainstem Responses", "hypotonia, congenital nystagmus, ataxia, and abnormal auditory brainstem responses", "HYPOTONIA, CONGENITAL NYSTAGMUS, ATAXIA, AND ABNORMAL AUDITORY BRAINSTEM RESPONSES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotonia, congenital nystagmus, ataxia, and abnormal auditory brainstem responses", "shortest_name_length": 80}
{"curie": "UMLS:C5419172", "names": ["COVID-19-Associated Stroke", "SARS-CoV-2-Associated Stroke", "COVID-19-Associated Cerebrovascular Accident", "SARS-CoV-2-Associated Cerebrovascular Accident"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "COVID-19-Associated Stroke", "shortest_name_length": 26}
{"curie": "UMLS:C2348369", "names": ["Early Favorable Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Early Favorable Hodgkin Lymphoma", "shortest_name_length": 32}
{"curie": "MONDO:0004266", "names": ["anal gland adenocarcinoma", "Anal Glands Adenocarcinoma", "anal glands adenocarcinoma", "Adenocarcinoma of anal ducts", "adenocarcinoma of anal gland", "adenocarcinoma of anal ducts", "Adenocarcinoma of Anal Gland", "Adenocarcinoma of anal glands", "adenocarcinoma of anal glands", "Adenocarcinoma of the Anal Gland", "adenocarcinoma of the anal gland", "adenocarcinoma of anal glands (diagnosis)", "Adenocarcinoma of anal glands (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anal gland adenocarcinoma", "shortest_name_length": 25}
{"curie": "UMLS:C3272476", "names": ["Ampulla of Vater Neuroendocrine Neoplasm", "Neuroendocrine Neoplasm of the Ampullary Region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ampulla of Vater Neuroendocrine Neoplasm", "shortest_name_length": 40}
{"curie": "MONDO:0021632", "names": ["Primary Brain Tumor", "primary brain tumor", "primary brain tumors", "brain tumors primary", "brain primary tumors", "Primary Brain Tumors", "Brain Tumor, Primary", "Primary Brain Neoplasm", "primary brain neoplasm", "Primary Brain Neoplasms", "Brain Neoplasm, Primary", "Localized Brain Neoplasm", "Brain Neoplasms, Primary", "Neoplasms, Brain, Primary", "Non-Metastatic Brain Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary brain neoplasm", "shortest_name_length": 19}
{"curie": "MONDO:0001650", "names": ["Acute cystitis", "cystitis acute", "Cystitis acute", "Cystitis;acute", "acute cystitis", "Acute Cystitis", "CYSTITIS, ACUTE", "acute; cystitis", "cystitis; acute", "cystitis, acute", "Cystitis acute NOS", "acute cystitis (disease)", "Acute cystitis (disorder)", "acute cystitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute cystitis", "shortest_name_length": 14}
{"curie": "MONDO:0007421", "names": ["Sellars Beighton syndrome", "Sellars-Beighton syndrome", "deafness-ear malformation-facial palsy syndrome", "Deafness-ear malformation-facial palsy syndrome", "Hearing loss-ear malformation-facial palsy syndrome", "Deafness with malformation of ear and facial palsy syndrome", "Deafness, Conductive Stapedial, with Ear Malformation and Facial Palsy", "Deafness with malformation of ear and facial palsy syndrome (disorder)", "DEAFNESS, CONDUCTIVE STAPEDIAL, WITH EAR MALFORMATION AND FACIAL PALSY", "deafness, conductive stapedial, with EAR malformation and facial palsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness-ear malformation-facial palsy syndrome", "shortest_name_length": 25}
{"curie": "UMLS:C3805233", "names": ["Post-ET Myelofibrosis", "Post-Essential Thrombocytosis Myelofibrosis", "Post essential thrombocythemia myelofibrosis", "Post-essential thrombocythemia myelofibrosis", "Post-Essential Thrombocythemia Myelofibrosis", "Post Essential Thrombocythemia Myelofibrosis", "Post-essential thrombocythaemia myelofibrosis", "Post essential thrombocythaemia myelofibrosis", "Myelofibrosis Transformation in Essential Thrombocythemia", "Myelofibrosis due to and following essential thrombocythemia", "Myelofibrosis due to and following essential thrombocythaemia", "Myelofibrosis due to and following essential thrombocythemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post-essential thrombocythemia myelofibrosis", "shortest_name_length": 21}
{"curie": "MONDO:0007721", "names": ["H hernia", "hiatus hernia", "Hiatus Hernia", "Hiatus hernia", "Hiatal Hernia", "Hernia hiatal", "hiatal hernia", "Hiatal hernia", "HIATAL HERNIA", "HERNIA HIATAL", "HIATUS HERNIA", "Hernia;hiatus", "Stomach hernia", "HERNIA, HIATUS", "Hernia, Hiatus", "Hernia, Hiatal", "Hiatal Hernias", "hernia; hiatal", "Hiatus Hernias", "Hernia, hiatal", "hernia, hiatus", "hiatal hernias", "hiatal; hernia", "Hernia, hiatus", "Hernias, Hiatus", "Hernias, Hiatal", "thoracic stomach", "Thoracic stomach", "esophageal hernia", "Esophageal hernia", "Esophageal Hernia", "hernia esophageal", "oesophageal hernia", "HH - Hiatus hernia", "Oesophageal hernia", "Esophageal Hernias", "Hernia, Esophageal", "Hernias, Esophageal", "Bergmann's syndrome", "paraesophageal hernia", "hernia paraesophageal", "HIATAL HERNIA SLIDING", "Hernia, diaphragmatic", "Sliding hiatus hernia", "Sliding hiatal hernia", "Rolling hiatal hernia", "Rolling hiatus hernia", "sliding hiatus hernia", "sliding hiatal hernia", "hernia sliding hiatus", "Sliding Hiatal Hernia", "Paraesophageal Hernia", "Paraesophageal hernia", "hiatal sliding hernia", "Sliding Hiatal Hernias", "paraesophageal; hernia", "Hiatal Hernia, Sliding", "Hernia, Paraesophageal", "Paraoesophageal hernia", "hernia; paraesophageal", "paraoesophageal hernia", "Hernia, Sliding Hiatal", "paraesophageal hernias", "Hiatus hernia syndrome", "Paraesophageal Hernias", "Hernias, Sliding Hiatal", "gastroesophageal hernia", "hiatus hernia (disease)", "Hernias, Paraesophageal", "Hiatal Hernias, Sliding", "Gastroesophageal hernia", "Esophageal hiatus hernia", "Gastrooesophageal hernia", "Esophageal hiatal hernia", "esophageal hiatal hernia", "Hernia, gastroesophageal", "Hiatal hernia (disorder)", "Hiatus hernia (diagnosis)", "Oesophageal hiatus hernia", "hiatal hernia (diagnosis)", "Sliding Esophageal Hernia", "Oesophageal hiatal hernia", "Hernia, Sliding Esophageal", "Sliding Esophageal Hernias", "Esophageal Hernia, Sliding", "Hernias, Sliding Esophageal", "Diaphragmatic/hiatus hernia", "Esophageal Hernias, Sliding", "Sliding diaphragmatic hernia", "Paraesophageal hiatal hernia", "Paraesophageal hiatus hernia", "Paraesophageal Hiatal Hernia", "paraesophageal hiatus hernia", "paraesophageal hiatal hernia", "thoracic stomach (diagnosis)", "Hernia, Paraesophageal Hiatal", "Paraoesophageal hiatal hernia", "Paraoesophageal hiatus hernia", "Paraesophageal Hiatal Hernias", "Hiatal Hernia, Paraesophageal", "Hernias, Paraesophageal Hiatal", "Diaphragmatic - hiatus -hernia", "diaphragmatic - hiatus -hernia", "Hiatal Hernias, Paraesophageal", "Paraesophageal hernia (disorder)", "Sliding hiatus hernia (disorder)", "Sliding esophageal hiatus hernia", "sliding hiatal hernia (diagnosis)", "Sliding oesophageal hiatus hernia", "hiatus hernia (esophageal) (sliding)", "paraesophageal hiatal hernia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hiatus hernia", "shortest_name_length": 8}
{"curie": "MONDO:0013789", "names": ["CDG1R", "CDGIr", "CDG-Ir", "CDG Ir", "DDOST-CDG", "DDOST-CDG (CDG-Ir)", "CDG syndrome type Ir", "congenital disorder of glycosylation Ir", "congenital disorder of glycosylation 1r", "DDOST-congenital disorder of glycosylation", "Congenital disorder of glycosylation type Ir", "congenital disorder of glycosylation type 1r", "Congenital disorder of glycosylation type 1r", "congenital disorder of glycosylation type Ir", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ir", "congenital disorder of glycosylation, type Ir", "carbohydrate deficient glycoprotein syndrome type", "Carbohydrate deficient glycoprotein syndrome type Ir", "carbohydrate deficient glycoprotein syndrome type Ir", "Congenital disorder of glycosylation type 1r (disorder)", "Congenital disorder of glycosylation type 1r (diagnosis)", "Dolichyl-diphosphooligosaccharide-protein glycosyltransferase congenital disorder of glycosylation", "DDOST-CDG - dolichyl-diphosphooligosaccharide-protein glycosyltransferase congenital disorder of glycosylation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DDOST-congenital disorder of glycosylation", "shortest_name_length": 5}
{"curie": "MONDO:0018814", "names": ["non-SCID", "non-SCID combined immunodeficiency", "non-severe combined immunodeficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-SCID combined immunodeficiency", "shortest_name_length": 8}
{"curie": "MONDO:0012335", "names": ["OBAIRH", "POMC deficiency", "POMC Deficiency", "PROOPIOMELANOCORTIN DEFICIENCY", "Proopiomelanocortin Deficiency", "PROOPIOMELANOCORTIN deficiency", "Pro-Opiomelanocortin Deficiency", "Pro-opiomelanocortin deficiency", "Proopiomelanocortin deficiency syndrome", "Obesity due to pro-opiomelanocortin deficiency", "obesity due to pro-opiomelanocortin deficiency", "Proopiomelanocortin deficiency syndrome (disorder)", "Obesity, early-onset, adrenal insufficiency, and red hair", "obesity, early-onset, adrenal insufficiency, and Red hair", "Obesity, Early-Onset, Adrenal Insufficiency, and Red Hair", "obesity, early-onset, with adrenal insufficiency and RED hair", "OBESITY, EARLY-ONSET, WITH ADRENAL INSUFFICIENCY AND RED HAIR", "obesity, early-onset, with adrenal insufficiency and Red hair", "obesity, adrenal insufficiency, and red hair due to POMC deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "obesity due to pro-opiomelanocortin deficiency", "shortest_name_length": 6}
{"curie": "MONDO:0020737", "names": ["OPA10", "optic atrophy 10", "optic atrophy 10 with or without ataxia, mental retardation, and seizures", "OPTIC ATROPHY 10 WITH OR WITHOUT ATAXIA, MENTAL RETARDATION, AND SEIZURES", "optic atrophy 10 with or without ataxia, intellectual disability, and seizures", "OPTIC ATROPHY 10 WITH OR WITHOUT ATAXIA, IMPAIRED INTELLECTUAL DEVELOPMENT, AND SEIZURES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "optic atrophy 10 with or without ataxia, intellectual disability, and seizures", "shortest_name_length": 5}
{"curie": "MONDO:0016566", "names": ["Loasis", "loasis", "LOIASIS", "loiasis", "Loiasis", "Loiases", "loaiasis", "Loaiasis", "Loaiases", "African eye worm", "Loa loa infection", "Loa loa Infection", "Loa loa Infections", "Loa loa Filariasis", "Loa loa Filariases", "Loa loa filariasis", "Infection, Loa loa", "loiasis (diagnosis)", "Filariasis, Loa loa", "infestation; eyeworm", "infestation; Loa loa", "Infection by Loa loa", "eyeworm; infestation", "Loa loa; infestation", "Eyeworm disease of Africa", "Infection caused by Loa loa", "Infection caused by Loa loa (disorder)", "disease (or disorder); eyeworm of Africa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "loiasis", "shortest_name_length": 6}
{"curie": "UMLS:C0586368", "names": ["Moderate Colon Dysplasia", "Moderate Colonic Dysplasia", "Moderate Dysplasia of Colon", "Moderate dysplasia of colon", "Moderate Dysplasia of the Colon", "Moderate dysplasia of colon (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Moderate dysplasia of colon", "shortest_name_length": 24}
{"curie": "MONDO:0020077", "names": ["Myeloproliferative-Myelodisplastic Disease", "myelodysplastic/myeloproliferative disease", "Myelodysplastic/myeloproliferative disease", "Myelodysplastic-Myeloproliferative Disease", "Myelodysplastic/Myeloproliferative Disease", "Myelodysplastic-Myeloproliferative Diseases", "Myeloproliferative Myelodisplastic Diseases", "Myelodysplastic/myeloproliferative diseases", "Myelodysplastic/Myeloproliferative Diseases", "Myeloproliferative-Myelodisplastic Diseases", "Disease, Myelodysplastic-Myeloproliferative", "Myelodysplastic/Myeloproliferative Disorder", "Myelodysplastic/Myeloproliferative Neoplasm", "Disease, Myeloproliferative-Myelodisplastic", "Myelodysplastic Myeloproliferative Diseases", "Myelodysplastic/myeloproliferative neoplasm", "Myelodysplastic/Myeloproliferative Disorders", "Diseases, Myeloproliferative-Myelodisplastic", "myelodysplastic/myeloproliferative neoplasms", "Diseases, Myelodysplastic-Myeloproliferative", "Myeloproliferative/Myelodysplastic Disorders", "Myeloproliferative/Myelodysplastic Syndromes", "Myelodysplastic/myeloproliferative disease (disorder)", "myelodysplastic/myeloproliferative disease (diagnosis)", "Myelodysplastic/myeloproliferative disease (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myelodysplastic/myeloproliferative disease", "shortest_name_length": 42}
{"curie": "MONDO:0015465", "names": ["CRMDD", "Schwartz-Lelek syndrome", "Craniometaphyseal dysplasia", "craniometaphyseal dysplasia", "CRANIOMETADIAPHYSEAL DYSPLASIA", "Craniometadiaphyseal dysplasia", "Craniometaphyseal dysplasia syndrome", "Craniometaphyseal dysplasia (disorder)", "Craniometadiaphyseal dysplasia (disorder)", "Genetic craniotubular bone dysplasias and hyperostoses"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniometaphyseal dysplasia", "shortest_name_length": 5}
{"curie": "UMLS:C1960870", "names": ["Chronic migraine", "Chronic Migraine", "Transformed migraine", "Transformed migraine (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transformed migraine", "shortest_name_length": 16}
{"curie": "MONDO:0003701", "names": ["nonencapsulated sclerosing tumor", "Nonencapsulated sclerosing tumor", "Nonencapsulated Sclerosing Tumor", "tumor; nonencapsulated sclerosing", "nonencapsulated; sclerosing tumor", "Nonencapsulated sclerosing tumour", "Nonencapsulated Sclerosing neoplasm", "nonencapsulated sclerosing neoplasm", "Nonencapsulated Sclerosing Neoplasm", "nonencapsulated sclerosing carcinoma", "Nonencapsulated Sclerosing Carcinoma", "Nonencapsulated sclerosing carcinoma", "nonencapsulated sclerosing; carcinoma", "carcinoma; nonencapsulated sclerosing", "papillary carcinoma, diffuse sclerosing", "Papillary carcinoma, diffuse sclerosing", "Nonencapsulated sclerosing adenocarcinoma", "nonencapsulated sclerosing adenocarcinoma", "Nonencapsulated Sclerosing Adenocarcinoma", "nonencapsulated; sclerosing adenocarcinoma", "adenocarcinoma; nonencapsulated sclerosing", "Thyroid Gland Diffuse Sclerosing Papillary Carcinoma", "thyroid gland diffuse sclerosing papillary carcinoma", "Nonencapsulated Sclerosing Papillary Thyroid Carcinoma", "nonencapsulated sclerosing papillary thyroid carcinoma", "Diffuse Sclerosing Variant Thyroid Gland Papillary Carcinoma", "Nonencapsulated sclerosing carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid gland diffuse sclerosing papillary carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0011376", "names": ["VF", "IVF", "VF1", "Idiopathic ventricular fibrillation", "Paroxysmal ventricular fibrillation", "ventricular fibrillation, familial, 1", "Paroxysmal familial ventricular fibrillation", "ventricular fibrillation paroxysmal familial", "Ventricular fibrillation, paroxysmal familial", "VENTRICULAR FIBRILLATION, PAROXYSMAL FAMILIAL, 1", "ventricular fibrillation, paroxysmal familial, 1", "Ventricular Fibrillation, Paroxysmal Familial, 1", "ventricular fibrillation, paroxysmal familial, type 1", "Paroxysmal familial ventricular fibrillation (disorder)", "Paroxysmal familial ventricular fibrillation (diagnosis)", "VENTRICULAR FIBRILLATION DURING MYOCARDIAL INFARCTION, SUSCEPTIBILITY TO", "ventricular fibrillation during myocardial infarction, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ventricular fibrillation, paroxysmal familial, type 1", "shortest_name_length": 2}
{"curie": "UMLS:C0030660", "names": ["pathologic process", "Pathologic Process", "pathological process", "Pathologic Processes", "Pathological process", "Processes, Pathologic", "pathological disorder", "Pathological Processes", "pathological processes", "pathological disorders", "PATHOLOGICAL DISORDERS", "Processes, Pathological", "Pathological process (attribute)", "Pathological process (qualifier value)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Processes", "shortest_name_length": 18}
{"curie": "MONDO:0006517", "names": ["Pediatric Cancer", "childhood cancer", "pediatric cancer", "cancer childhood", "cancer pediatric", "Childhood Cancer", "cancer, childhood", "cancers childhood", "cancers pediatric", "cancer pediatrics", "Cancer in Children", "Cancer in children", "Malignant Neoplasm", "malignant neoplasm", "pediatric neoplasm", "Malignant Pediatric Tumor", "Malignant Childhood Tumor", "pediatric neoplasm/cancer", "malignant pediatric tumor", "malignant childhood tumor", "malignant pediatric neoplasm", "malignant childhood neoplasm", "Malignant Childhood Neoplasm", "Childhood Malignant Neoplasm", "childhood malignant neoplasm", "Malignant Pediatric Neoplasm", "childhood neoplasm, malignant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood malignant neoplasm", "shortest_name_length": 16}
{"curie": "UMLS:C2609176", "names": ["Kounis syndrome", "Kounis Syndrome", "Allergic Angina Syndrome", "Allergic Angina Syndromes", "Allergic Acute Coronary Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kounis Syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0044709", "names": ["cochleovestibular dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cochleovestibular dysplasia", "shortest_name_length": 27}
{"curie": "UMLS:C4528213", "names": ["Type E LyP", "Type E Lymphomatoid Papulosis", "Angioinvasive Lymphomatoid Papulosis Type E"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Type E Lymphomatoid Papulosis", "shortest_name_length": 10}
{"curie": "MONDO:0021915", "names": ["Arakawa syndrome 2", "arakawa syndrome 2", "Arakawa Syndrome II", "Arakawa syndrome II", "Arakawa's syndrome 2", "Arakawa's Syndrome 2", "Arakawa's syndrome II", "Arakawa's Syndrome II", "Methionine Synthase Deficiency", "Methionine synthase deficiency", "methionine synthase deficiency", "THF methyltransferase deficiency", "methylcobalamin deficiency, cblG type", "Methylcobalamin Deficiency, cblG Type", "N5-methylhomocysteine transferase deficiency", "Tetrahydrofolate methyltransferase deficiency", "Tetrahydrofolate Methyltransferase Deficiency", "tetrahydrofolate methyltransferase deficiency", "tetrahydrofolate-methyltransferase deficiency syndrome", "Tetrahydrofolate-methyltransferase deficiency syndrome", "Tetrahydrofolate methyltransferase deficiency (disorder)", "homocystinuria-megaloblastic Anemia, cblG complementation type", "Homocystinuria-Megaloblastic Anemia, cblG Complementation Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arakawa syndrome 2", "shortest_name_length": 18}
{"curie": "UMLS:C3897541", "names": ["Stage IA Esophageal Cancer", "Stage IA Esophageal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Esophageal Cancer AJCC v7", "shortest_name_length": 26}
{"curie": "UMLS:C0235969", "names": ["ejaculation disorder", "Ejaculation disorder", "Ejaculation Disorder", "EJACULATION DISORDER", "disorders ejaculation", "Ejaculation Dysfunction", "Disorder of ejaculation", "Ejaculatory Dysfunction", "Ejaculation disorder NOS", "Ejaculation disorder, NOS", "Disorder of ejaculation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disorder of ejaculation", "shortest_name_length": 20}
{"curie": "MONDO:0006773", "names": ["gonadal tissue neoplasm", "Gonadal Tissue Neoplasm", "Neoplasm, Gonadal Tissue", "Tissue Neoplasm, Gonadal", "Gonadal Tissue Neoplasms", "Neoplasms, Gonadal Tissue", "Tissue Neoplasms, Gonadal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gonadal tissue neoplasm", "shortest_name_length": 23}
{"curie": "MONDO:0005229", "names": ["bacteremia", "BACTEREMIA", "Bacteremia", "Bacteraemia", "Bacteremias", "bacteriemia", "bacteraemia", "bacteremias", "Bacteremia, NOS", "blood poisoning", "bacterial sepsis", "Bacteremia (finding)", "bacteria in the blood", "Unspecified bacteremia", "bacteremia (diagnosis)", "symptomatic bacteremia", "Unspecified bacteraemia", "Bacteremia, unspecified", "Bacteraemia, unspecified", "Bacteria in blood culture", "Bacteria in blood cultures", "bacterial infectious disease with sepsis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bacterial infectious disease with sepsis", "shortest_name_length": 10}
{"curie": "UMLS:C0347012", "names": ["Metastasis to urethra", "Metastasis to the Urethra", "Metastatic tumor to urethra", "Metastatic tumour to urethra", "Metastatic Neoplasm to the Urethra", "urethra neoplasm malignant secondary", "Secondary malignant neoplasm of urethra", "Metastatic malignant neoplasm of urethra", "Metastatic malignant neoplasm to urethra", "Metastatic Malignant Neoplasm in the Urethra", "Metastatic Malignant Neoplasm to the Urethra", "Metastatic malignant neoplasm to urethra (disorder)", "Secondary malignant neoplasm of urethra (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to urethra", "shortest_name_length": 21}
{"curie": "MONDO:0007551", "names": ["EBS1C", "DEBS-WC", "EBS-loc", "Localized EBS", "Weber-Cockayne", "Acral Form EBS", "EBS, Acral Form", "EBS, acral form", "Acral Form EBSs", "EBS, ACRAL FORM", "EBSs, Acral Form", "weber cockayne syndrome", "cockayne weber syndrome", "Weber-Cockayne syndrome", "Weber Cockayne Syndrome", "Weber-Cockayne Syndrome", "Weber-Cockayne epidermolysis bullosa", "epidermolysis bullosa of hands and feet", "EPIDERMOLYSIS BULLOSA OF HANDS AND FEET", "localized epidermolysis bullosa simplex", "Epidermolysis Bullosa of Hands and Feet", "Localized epidermolysis bullosa simplex", "epidermolysis bullosa simplex, localized", "Epidermolysis Bullosa Simplex, Localized", "EPIDERMOLYSIS BULLOSA SIMPLEX 1C, LOCALIZED", "epidermolysis bullosa simplex 1C, localized", "epidermolysis bullosa simplex localized type", "Epidermolysis bullosa simplex of palms and soles", "epidermolysis bullosa simplex of palms and soles", "epidermolysis bullosa simplex Weber-Cockayne type", "Weber-Cockayne type epidermolysis bullosa simplex", "Weber-Cockayne Type Epidermolysis Bullosa Simplex", "Weber Cockayne Type Epidermolysis Bullosa Simplex", "Epidermolysis bullosa simplex, Weber-Cockayne type", "Epidermolysis Bullosa Simplex, Weber-Cockayne Type", "epidermolysis bullosa simplex, Weber-Cockayne type", "Epidermolysis Bullosa Simplex, Weber Cockayne Type", "Epidermolysis bullosa simplex of the hands and feet", "EPIDERMOLYSIS BULLOSA SIMPLEX 1C, WEBER-COCKAYNE TYPE", "Epidermolysis Bullosa Simplex, Cockayne Touraine Type", "Epidermolysis Bullosa Simplex, Cockayne-Touraine Type", "Epidermolysis bullosa simplex - Weber-Cockayne variety", "Epidermolysis bullosa simplex of the hands AND/OR feet", "Dominant epidermolysis bullosa simplex, Weber-Cockayne type", "Dominant epidermolysis bullosa simplex, Weber-Cockayne type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolysis bullosa simplex 1C, localized", "shortest_name_length": 5}
{"curie": "MONDO:0019836", "names": ["congenital anomaly of hepatic vein"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital anomaly of hepatic vein", "shortest_name_length": 34}
{"curie": "MONDO:0015476", "names": ["cysts and fistulae of the face and oral cavity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cysts and fistulae of the face and oral cavity", "shortest_name_length": 46}
{"curie": "MONDO:0017062", "names": ["spina bifida aperta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spina bifida aperta", "shortest_name_length": 19}
{"curie": "MONDO:0013407", "names": ["RP47", "retinitis pigmentosa 47", "RETINITIS PIGMENTOSA 47", "SAG retinitis pigmentosa", "retinitis pigmentosa type 47", "retinitis pigmentosa caused by mutation in SAG"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 47", "shortest_name_length": 4}
{"curie": "UMLS:C3273033", "names": ["Well Differentiated Hepatocellular Cancer", "Well Differentiated Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Well Differentiated Hepatocellular Carcinoma", "shortest_name_length": 41}
{"curie": "UMLS:C0040101", "names": ["Thymoma benign", "benign thymoma", "Benign Thymoma", "thymoma benign", "THYMOMA BENIGN", "Benign thymoma", "Thymoma, benign", "Benign thymoma (disorder)", "Thymoma, benign (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Thymoma", "shortest_name_length": 14}
{"curie": "MONDO:0021234", "names": ["SPINE TUMOR", "spinal tumor", "Spinal tumor", "Spinal tumors", "spinal tumour", "Spinal tumour", "spinal tumors", "spinal tumours", "Spinal tumours", "Spinal Neoplasm", "Spinal Neoplasms", "Neoplasm, Spinal", "Spinal Cord Tumor", "spinal cord tumor", "Neoplasms, Spinal", "Spinal cord tumor", "tumor of vertebra", "Spinal Cord Tumors", "spinal cord tumors", "Tumor, Spinal Cord", "Spinal cord tumour", "Spinal cord--Tumors", "Tumors, Spinal Cord", "Tumor of Spinal Cord", "Spinal cord neoplasm", "tumor of spinal cord", "neoplasm of vertebra", "Tumor of spinal cord", "spinal cord neoplasm", "Neoplasm of vertebra", "Spinal Cord Neoplasm", "Neoplasm, Spinal Cord", "Tumour of spinal cord", "Spinal Cord Neoplasms", "Neoplasms, Spinal Cord", "Neoplasm of Spinal Cord", "Neoplasm of spinal cord", "neoplasm of spinal cord", "Tumor of the Spinal Cord", "Tumor of the spinal cord", "tumor of the spinal cord", "Spinal cord neoplasm NOS", "Tumour of the spinal cord", "Neoplasm of the Spinal Cord", "neoplasm of the spinal cord", "spinal cord tumor (diagnosis)", "spinal cord neoplasm (disease)", "Neoplasm of vertebra (disorder)", "neoplasm of vertebra (diagnosis)", "Neoplasm of spinal cord (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal cord neoplasm", "shortest_name_length": 11}
{"curie": "MONDO:0011213", "names": ["PRPTS", "PIERPONT SYNDROME", "Pierpont syndrome", "PIERPONT syndrome", "Pierpont syndrome (disorder)", "plantar lipomatosis, unusual facies, and developmental delay", "Plantar Lipomatosis, Unusual Facies, and Developmental Delay", "PLANTAR LIPOMATOSIS, UNUSUAL FACIES, AND DEVELOPMENTAL DELAY", "plantar lipomatosis-unusual facies-developmental delay syndrome", "Plantar lipomatosis-unusual facies-developmental delay syndrome", "plantar lipomatosis-facial dysmorphism-developmental delay syndrome", "Plantar lipomatosis-facial dysmorphism-developmental delay syndrome", "Plantar lipomatosis, facial dysmorphism, developmental delay syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pierpont syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0004733", "names": ["pyriform sinus cancer", "PYRIFORM SINUS CANCER", "Malignant Pyriform Fossa Tumor", "Malignant Pyriform Sinus Tumor", "malignant pyriform sinus tumor", "malignant pyriform fossa tumor", "PYRIFORM SINUS CANCER MALIGNANT", "Malignant Pyriform Sinus Neoplasm", "malignant tumor of pyriform fossa", "Malignant tumor of pyriform fossa", "malignant pyriform sinus neoplasm", "malignant pyriform fossa neoplasm", "Malignant Pyriform Fossa Neoplasm", "malignant tumor of pyriform sinus", "Malignant tumor of pyriform sinus", "Malignant Tumor of Pyriform Fossa", "Malignant Tumor of Pyriform Sinus", "Malignant tumour of pyriform sinus", "Malignant tumour of pyriform fossa", "Malignant neoplasm of pyriform sinus", "malignant neoplasm of pyriform fossa", "Malignant Neoplasm of Pyriform Sinus", "malignant neoplasm of pyriform sinus", "Malignant Neoplasm of Pyriform Fossa", "Malignant neoplasm of pyriform fossa", "Malignant Tumor of the Pyriform Sinus", "malignant tumor of the pyriform fossa", "malignant tumor of the pyriform sinus", "Malignant Tumor of the Pyriform Fossa", "malignant neoplasm of the pyriform sinus", "Malignant Neoplasm of the Pyriform Sinus", "malignant neoplasm of the Pyriform Fossa", "Malignant Neoplasm of the Pyriform Fossa", "malignant neoplasm of the pyriform fossa", "Malignant tumor of pyriform fossa (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyriform sinus cancer", "shortest_name_length": 21}
{"curie": "MONDO:0013928", "names": ["DYT23", "dystonia 23", "DYSTONIA 23", "Dystonia 23", "dystonia type 23", "CACNA1B dystonic disorder", "Adult-onset cervical dystonia DYT23 type", "adult-onset cervical dystonia, DYT23 type", "Adult-onset cervical dystonia, DYT23 type", "dystonic disorder caused by mutation in CACNA1B", "Adult-onset cervical dystonia DYT23 type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dystonia 23", "shortest_name_length": 5}
{"curie": "MONDO:0017048", "names": ["PMP", "Adenomucinosis", "mucinous ascites", "myxoma peritonei", "Myxoma peritonei", "mucinous Ascites", "Myxoma Peritonei", "Mucinous Ascites", "Gelatinous ascites", "gelatinous ascites", "Gelatinous Ascites", "Ascites, Gelatinous", "PSEUDOMYXOMA PERITONEI", "Pseudomyxoma peritonei", "pseudomyxoma peritonei", "Pseudomyxoma Peritonei", "PERITONITIS, MYXOMATOUS", "[M]Pseudomyxoma peritonei", "Pseudomyxoma Peritonei Syndrome", "malignant pseudomyxoma peritonei", "Pseudomyxoma Peritonei Syndromes", "Pseudomyxoma peritonei (disorder)", "syndrome of pseudomyxoma peritonei", "Syndrome of Pseudomyxoma Peritonei", "pseudomyxoma peritonei of peritoneum", "peritoneal cavity pseudomyxoma peritonei", "Peritoneal Cavity Pseudomyxoma Peritonei", "malignant peritoneal pseudomyxoma peritonei", "pseudomyxoma peritonei (morphologic abnormality)", "pseudomyxoma peritonei of peritoneum (diagnosis)", "Pseudomyxoma peritonei (morphologic abnormality)", "well differentiated peritoneal mucinous adenocarcinoma", "Well Differentiated Peritoneal Mucinous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudomyxoma peritonei", "shortest_name_length": 3}
{"curie": "MONDO:0000756", "names": ["parameningeal embryonal rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parameningeal embryonal rhabdomyosarcoma", "shortest_name_length": 40}
{"curie": "UMLS:C0022361", "names": ["jaw cyst", "cyst jaw", "Jaw cyst", "Jaw Cyst", "Cyst, Jaw", "cyst jaws", "cyst; jaw", "Jaw Cysts", "jaw cysts", "cysts jaw", "jaw; cyst", "Cysts, Jaw", "Jaws--Cysts", "Cyst of jaw", "cyst of jaw", "Cyst of jaw NOS", "Cyst of jaw, NOS", "Cyst of jaw (disorder)", "cyst of jaw (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jaw Cysts", "shortest_name_length": 8}
{"curie": "MONDO:0004944", "names": ["cns syphilis", "syphilis cns", "Neurosyphilis", "NEUROSYPHILIS", "Syphilis, CNS", "neurosyphilis", "neurosyphilitic", "late neurosyphilis", "Neurosyphilis, NOS", "cerebrospinal syphilis", "syphilis cerebrospinal", "tertiary neurosyphilis", "syphilis; cerebrospinal", "syphilis; nervous system", "Neurosyphilis (disorder)", "cerebrospinal; syphilitic", "neurosyphilis (diagnosis)", "Neurosyphilis, unspecified", "nervous system; syphilitic", "Central Nervous System Syphilis", "Syphilis, Central Nervous System", "syphilis; central nervous system", "Syphilis of central nervous system", "cerebrospinal syphilis (diagnosis)", "central nervous system; syphilitic", "Syphilis of central nervous system NOS", "Syphilis of central nervous system, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurosyphilis", "shortest_name_length": 12}
{"curie": "UMLS:C0334573", "names": ["AFS", "Ameloblastic sarcoma", "ameloblastic; sarcoma", "sarcoma; ameloblastic", "Odontogenic fibrosarcoma", "Ameloblastic fibrosarcoma", "Ameloblastic Fibrosarcoma", "odontogenic; fibrosarcoma", "fibrosarcoma; odontogenic", "fibrosarcoma; ameloblastic", "ameloblastic; fibrosarcoma", "Ameloblastic fibrosarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ameloblastic Fibrosarcoma", "shortest_name_length": 3}
{"curie": "MONDO:0014369", "names": ["CJS", "PHS2, FORMERLY", "Culler-Jones syndrome", "CULLER-JONES SYNDROME", "Pallister-Hall syndrome 2", "Pallister-Hall syndrome 2, formerly", "PALLISTER-HALL SYNDROME 2, FORMERLY", "postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome", "Postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0010194", "names": ["WMS1", "WEILL-MARCHESANI SYNDROME 1", "Weill-Marchesani syndrome 1", "Weill-Marchesani syndrome type 1", "ADAMTS10 Weill-Marchesani syndrome", "spherophakia-brachymorphia syndrome", "SPHEROPHAKIA-BRACHYMORPHIA SYNDROME", "Weill-Marchesani syndrome 1, recessive", "mesodermal Dysmorphodystrophy, congenital", "MESODERMAL DYSMORPHODYSTROPHY, CONGENITAL", "Weill Marchesani Syndrome, Autosomal Recessive", "WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE", "Weill-Marchesani syndrome, autosomal recessive", "Weill-Marchesani Syndrome, Autosomal Recessive", "Weill-Marchesani syndrome caused by mutation in ADAMTS10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Weill-Marchesani syndrome 1", "shortest_name_length": 4}
{"curie": "UMLS:C0476171", "names": ["Comminuted", "comminuted", "[Q] Comminuted", "Comminuted Fracture", "comminuted fracture", "Comminuted fracture", "Fracture, comminuted", "Fracture, Comminuted", "Comminuted Fractures", "comminuted fractures", "Comminuted fractures", "Fractures, Comminuted", "Comminuted Fracture type", "Fracture, comminuted (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Comminuted Fracture type", "shortest_name_length": 10}
{"curie": "MONDO:0014385", "names": ["AI2A5", "SLC24A4 amelogenesis imperfecta", "amelogenesis imperfecta type IIA5", "amelogenesis imperfecta, type IIA5", "amelogenesis imperfecta hypomaturation type 2A5", "amelogenesis imperfecta hypomaturation type IIA5", "AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA5", "amelogenesis imperfecta, hypomaturation type, IIA5", "amelogenesis imperfecta caused by mutation in SLC24A4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amelogenesis imperfecta hypomaturation type 2A5", "shortest_name_length": 5}
{"curie": "MONDO:0010207", "names": ["SALAMON SYNDROME", "Salamon Syndrome", "Salamon syndrome", "Salamon's syndrome", "Salamon's syndrome (disorder)", "woolly hair hypotrichosis everted lower lip and outstanding ears", "Woolly hair, hypotrichosis, everted lower lip and outstanding ears", "WOOLLY HAIR, HYPOTRICHOSIS, EVERTED LOWER LIP, AND OUTSTANDING EARS", "woolly hair, hypotrichosis, everted LOWER LIP, and outstanding ears", "Woolly Hair, Hypotrichosis, Everted Lower Lip, And Outstanding Ears", "wooly hair-hypotrichosis-everted lower lip-outstanding ears syndrome", "woolly hair-hypotrichosis-everted lower lip-outstanding ears syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "woolly hair-hypotrichosis-everted lower lip-outstanding ears syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0017694", "names": ["GSD type 2, infantile onset", "GSD type II, infantile onset", "Pompe disease, infantile onset", "Pompe's disease infantile onset", "glycogenosis type 2, infantile onset", "Glycogenosis type 2, infantile onset", "glycogenosis type II, infantile onset", "Glycogenosis type II, infantile onset", "Glycogen storage disease type II infantile onset", "Glycogen storage disease type 2, infantile onset", "glycogen storage disease type 2, infantile onset", "Glycogen storage disease type II, infantile onset", "glycogen storage disease type II, infantile onset", "GSD due to acid maltase deficiency, infantile onset", "Alpha-1,4-glucosidase acid deficiency, infantile onset", "alpha-1,4-glucosidase acid deficiency, infantile onset", "Glycogen storage disease type II infantile onset (disorder)", "glycogenosis due to acid maltase deficiency, infantile onset", "Glycogenosis due to acid maltase deficiency, infantile onset", "Glycogen storage disease due to acid maltase deficiency, infantile onset", "glycogen storage disease due to acid maltase deficiency, infantile onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease due to acid maltase deficiency, infantile onset", "shortest_name_length": 27}
{"curie": "MONDO:0004290", "names": ["subglottic verrucous carcinoma", "subglottis verrucous carcinoma", "Subglottis Verrucous Carcinoma", "Subglottic Verrucous Carcinoma", "verrucous carcinoma of Subglottis", "Verrucous Carcinoma of Subglottis", "verrucous carcinoma of subglottis", "verrucous carcinoma of the subglottis", "Verrucous Carcinoma of the Subglottis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subglottis verrucous carcinoma", "shortest_name_length": 30}
{"curie": "MONDO:0021298", "names": ["oropharynx cancer, stage 0", "Cancer in situ of oropharynx", "oropharyngeal cancer stage 0", "Oropharynx Carcinoma in situ", "stage 0 oropharynx carcinoma", "Carcinoma situ of oropharynx", "Stage 0 Oropharyngeal Cancer", "stage 0 oropharyngeal cancer", "Stage 0 Oropharynx Carcinoma", "oropharynx carcinoma in situ", "oropharynx in situ carcinoma", "Oropharyngeal Cancer Stage 0", "Oropharyngeal cancer stage 0", "oropharyngeal cancer, stage 0", "Carcinoma in situ of oropharynx", "oropharyngeal carcinoma in situ", "Oropharyngeal Carcinoma in situ", "Stage 0 Oropharyngeal Carcinoma", "stage 0 carcinoma of oropharynx", "Carcinoma in situ of Oropharynx", "Stage 0 Carcinoma of Oropharynx", "carcinoma in situ of oropharynx", "stage 0 oropharyngeal carcinoma", "Carcinoma in situ of mesopharynx", "Stage 0 Oropharyngeal Throat Cancer", "stage 0 oropharyngeal throat cancer", "Carcinoma in situ of the Oropharynx", "stage 0 carcinoma of the oropharynx", "Stage 0 Carcinoma of the Oropharynx", "carcinoma in situ of the oropharynx", "Carcinoma in situ of oropharynx, NOS", "stage 0 oropharyngeal carcinoma aJCC v6", "Stage 0 Oropharyngeal Carcinoma AJCC v7", "stage 0 oropharyngeal carcinoma in situ", "Stage 0 Oropharyngeal Carcinoma AJCC v6", "stage 0 oropharyngeal carcinoma aJCC v7", "Carcinoma in situ of oropharynx (disorder)", "carcinoma in situ of oropharynx (diagnosis)", "Stage 0 Oropharyngeal Carcinoma AJCC v6 and v7", "stage 0 oropharyngeal carcinoma aJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma in situ of oropharynx", "shortest_name_length": 26}
{"curie": "OMIM:607514", "names": ["BMIQ10", "OBESITY, SUSCEPTIBILITY TO", "BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 6}
{"curie": "MONDO:0007422", "names": ["KHM", "VOWNKL", "Vohwinkel syndrome", "VOHWINKEL SYNDROME", "Ppk Mutilans Vohwinkel", "Mutilating keratoderma", "mutilating keratoderma", "MUTILATING KERATODERMA", "Keratoderma, mutilating", "PPK mutilans and deafness", "PPK mutilans and hearing loss", "Mutilating keratoderma (disorder)", "KERATODERMA HEREDITARIUM MUTILANS", "Palmoplantar Keratoderma Mutilans", "Keratoderma hereditarium mutilans", "keratoderma hereditarium mutilans", "Vohwinkel's mutilating keratoderma", "mutilating keratoderma of Vohwinkel", "Mutilating keratoderma of Vohwinkel", "Mutilating keratoderma plus deafness", "mutilating keratoderma plus deafness", "Mutilating keratoderma plus hearing loss", "Palmoplantar Keratoderma Mutilans Vohwinkel", "mutilating keratoderma of Vohwinkel (diagnosis)", "Congenital Deafness with Keratopachydermia and Constrictions of Fingers and Toes", "congenital deafness with keratopachydermia and constrictions fo fingers and toes", "DEAFNESS, CONGENITAL, WITH KERATOPACHYDERMIA AND CONSTRICTIONS OF FINGERS AND TOES", "deafness, congenital, with KERATOPACHYDERMIA and constrictions of fingers and toes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratoderma hereditarium mutilans", "shortest_name_length": 3}
{"curie": "MONDO:0019622", "names": ["NSIP", "nonspecific interstitial pneumonia", "Nonspecific interstitial pneumonia", "Nonspecific Interstitial Pneumonia", "interstitial pneumonia nonspecific", "Non-specific interstitial pneumonia", "non-specific interstitial pneumonia", "Nonspecific interstitial pneumonitis", "Non-specific interstitial pneumonia NOS", "Temporally uniform pulmonary inflammation", "Nonspecific interstitial pneumonia (disorder)", "Non-specific idiopathic interstitial pneumonia", "interstitial pneumonia nonspecific (diagnosis)", "non-specific idiopathic interstitial pneumonia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-specific interstitial pneumonia", "shortest_name_length": 4}
{"curie": "MONDO:0004471", "names": ["PYARTHROSIS", "Pyarthrosis", "pyarthrosis", "pyoarthrosis", "Pyoarthrosis", "Infected joint", "septic arthrits", "ARTHRITIS SEPTIC", "Arthritis septic", "septic arthritis", "Septic arthritis", "SEPTIC ARTHRITIS", "Septic Arthritis", "Arthritis;septic", "arthritis septic", "arthritis; septic", "Pyoarthrosis, NOS", "septic; arthritis", "Arthritis, Septic", "ARTHRITIS, SEPTIC", "ARTHRITIS PYOGENIC", "Arthritis;pyogenic", "Purulent arthritis", "purulent arthritis", "Pyogenic Arthritis", "PYOGENIC ARTHRITIS", "pyogenic arthritis", "Arthritis pyogenic", "Pyogenic arthritis", "Bacterial arthritis", "ARTHRITIS, PYOGENIC", "infective arthritis", "Infective arthritis", "Arthritis bacterial", "Infective Arthritis", "ARTHRITIS, PURULENT", "Arthritis infective", "purulent; arthritis", "arthritis; purulent", "bacterial arthritis", "Bacterial Arthritis", "infection; arthritis", "ARTHRITIS INFECTIOUS", "Infectious Arthritis", "arthritis infectious", "infectious arthritis", "Infectious arthritis", "arthritis; infection", "Arthritis, Bacterial", "Septic arthritis NOS", "INFECTIOUS ARTHRITIS", "arthritis; bacterial", "bacterium; arthritis", "Bacterial Arthritides", "ARTHRITIS, INFECTIOUS", "arthritis suppurative", "infectious; arthritis", "Septic arthritis, NOS", "Suppurative Arthritis", "Suppurative arthritis", "Arthritis, Infectious", "suppurative arthritis", "Arthritides, Bacterial", "Arthritis, Suppurative", "ARTHRITIS, SUPPURATIVE", "arthritis; suppurative", "suppurative; arthritis", "Pyogenic arthritis, NOS", "Arthritis infective NOS", "Arthritis bacterial NOS", "Infective arthritis NOS", "Infective arthritis, NOS", "Bacterial arthritis, NOS", "septic arthritis (diagnosis)", "Bacterial arthritis (disorder)", "Infective arthritis (disorder)", "Infection-associated arthritis", "Unspecified infective arthritis", "infective arthritis (diagnosis)", "Pyogenic arthritis, unspecified", "Suppurative arthritis (disorder)", "infectious; arthritis (etiology)", "Arthritis due to direct infection", "arthritis; infectious or infective", "Arthritis due to bacterial infection", "Unspecified infective arthritis, hand", "infectious; arthritis (manifestation)", "Infective arthritis of shoulder region", "Infective arthritis or polyarthritis NOS", "Unspecified infective arthritis, forearm", "arthritis; infectious disease (etiology)", "Unspecified infective arthritis, lower leg", "Unspecified infective arthritis, upper arm", "arthritis; infectious disease (manifestation)", "Unspecified infective arthritis involving hand", "Unspecified infective arthritis, ankle and foot", "Unspecified infective arthritis, shoulder region", "Infective arthritis of shoulder region (disorder)", "Unspecified infective arthritis involving forearm", "Unspecified infective arthritis, site unspecified", "Pyogenic arthritis, unspecified, site unspecified", "Unspecified infective arthritis involving upper arm", "Unspecified infective arthritis involving lower leg", "Unspecified infective arthritis involving ankle and foot", "Unspecified infective arthritis, pelvic region and thigh", "Unspecified infective arthritis involving shoulder region", "Unspecified infective arthritis involving pelvic region and thigh"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bacterial arthritis", "shortest_name_length": 11}
{"curie": "MONDO:0056813", "names": ["Hormone-Resistant Breast Cancer", "hormone-resistant breast cancer", "hormone-refractory breast cancer", "Hormone refractory breast cancer", "Hormone-Refractory Breast Cancer", "hormone-resistant breast carcinoma", "Hormone-Resistant Breast Carcinoma", "Hormone-Resistant Breast Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hormone-resistant breast carcinoma", "shortest_name_length": 31}
{"curie": "MONDO:0006955", "names": ["RHD", "rhd", "Rheumatic carditis", "rheumatic carditis", "carditis rheumatic", "Rheumatic pancarditis", "pancarditis; rheumatic", "rheumatic; pancarditis", "Pancarditis, rheumatic", "Disease;rheumatic heart", "Rheumatic heart disease", "RHEUMATIC HEART DISEASE", "Rheumatic carditis, NOS", "Rheumatic Heart Disease", "disease heart rheumatic", "rheumatic heart disease", "Chronic rheumatic fever", "heart disease rheumatoid", "Rheumatic Heart Diseases", "RHEUMATOID HEART DISEASE", "rheumatic heart diseases", "rheumatoid heart disease", "Rheumatoid heart disease", "heart disease, rheumatic", "Disease, Rheumatic Heart", "disease, rheumatic heart", "Heart Disease, Rheumatic", "Heart Diseases, Rheumatic", "Diseases, Rheumatic Heart", "heart; disease, rheumatic", "Rheumatic heart disease NOS", "Rheumatic heart disease, NOS", "disease fever heart rheumatic", "fever rheumatic heart disease", "heart disease rheumatic fever", "Chronic rheumatic heart disease", "Rheumatic heart disease (disorder)", "rheumatic heart disease (diagnosis)", "Unspecified rheumatic heart disease", "Rheumatic heart disease, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rheumatic heart disease", "shortest_name_length": 3}
{"curie": "UMLS:C4552016", "names": ["Stage IIIA", "stage IIIA cancer of testis", "Stage IIIA Cancer of Testis", "Stage IIIA Testicular Cancer", "Testicular Cancer Stage IIIA", "stage IIIA testicular cancer", "Stage IIIA Cancer of the Testis", "stage IIIA cancer of the testis", "Stage IIIA Testicular Cancer AJCC v7", "stage IIIA testicular cancer AJCC v6", "stage IIIA testicular cancer AJCC v7", "Stage IIIA Testicular Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Testicular Cancer AJCC v6 and v7", "shortest_name_length": 10}
{"curie": "UMLS:C1848922", "names": ["HexA Deficiency", "Hexosaminidase A Deficiency", "Deficiency, Hexosaminidase A", "Hexosaminidase alpha-Subunit Deficiency (Variant B)", "Hexosaminidase alpha Subunit Deficiency (Variant B)", "Deficiency, Hexosaminidase alpha-Subunit (Variant B)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hexosaminidase alpha-Subunit Deficiency (Variant B)", "shortest_name_length": 15}
{"curie": "MONDO:0032619", "names": ["MC1DN14", "nuclear type mitochondrial complex I deficiency 14", "mitochondrial complex 1 deficiency, nuclear type 14", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 14", "shortest_name_length": 7}
{"curie": "MONDO:0013527", "names": ["LIS4", "LISSENCEPHALY 4", "lissencephaly 4", "lissencephaly type 4", "NDE1 lissencephaly (disease)", "LISSENCEPHALY 4 WITH MICROCEPHALY", "lissencephaly 4 with microcephaly", "lissencephaly 4, with microcephaly", "lissencephaly 4 (with microcephaly)", "lissencephaly (disease) caused by mutation in NDE1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lissencephaly 4", "shortest_name_length": 4}
{"curie": "MONDO:0004224", "names": ["Chronic Metabolic Polyneuropathy", "chronic metabolic polyneuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic metabolic polyneuropathy", "shortest_name_length": 32}
{"curie": "MONDO:0002272", "names": ["Polyclonal Hypergammaglobulinemia", "Polyclonal hypergammaglobulinemia", "polyclonal hypergammaglobulinemia", "hypergammaglobulinemia polyclonal", "hypergammaglobulinemia; polyclonal", "polyclonal; hypergammaglobulinemia", "Polyclonal hypergammaglobulinaemia", "Polyclonal hypergammaglobulinemia (disorder)", "polyclonal hypergammaglobulinemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyclonal hypergammaglobulinemia", "shortest_name_length": 33}
{"curie": "UMLS:C5237031", "names": ["Upper Aerodigestive Invasive Malignancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Upper Aerodigestive Invasive Malignancy", "shortest_name_length": 39}
{"curie": "MONDO:0008130", "names": ["Levic Stefanovic Nikolic syndrome", "Levic-Stefanovic-Nikolic syndrome", "ophthalmoplegia-intellectual disability-lingua scrotalis syndrome", "OPHTHALMOPLEGIA, PROGRESSIVE, WITH SCROTAL TONGUE AND MENTAL DEFICIENCY", "ophthalmoplegia, progressive, with scrotal tongue and mental deficiency", "Ophthalmoplegia, Progressive, with Scrotal Tongue and Mental Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ophthalmoplegia-intellectual disability-lingua scrotalis syndrome", "shortest_name_length": 33}
{"curie": "MONDO:0006019", "names": ["yaw", "pian", "PIAN", "yaws", "Yaws", "Buba", "YAWS", "Pian", "Bouba", "BOUBA", "bouba", "yawing", "parangi", "PARANGI", "thymosis", "Frambesia", "frambesia", "Yaws, NOS", "frambosie", "FRAMBESIA", "Castellani", "Frambesias", "Framboesia", "framboesia", "Yaws (disorder)", "frambesia tropica", "Yaws, unspecified", "Frambesia Tropica", "Frambesia Tropicas", "frambesia (tropica)", "endemic treponematoses", "polypapilloma tropicum", "yaws (Treponema pertenue)", "Treponema pertenue infection", "Infection by Treponema pertenue", "yaws (Treponema pertenue) (diagnosis)", "Treponema pallidum subsp. pertenue infectious disease", "Treponema pallidum subsp. pertenue disease or disorder", "Treponema pallidum subsp. pertenue caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "yaws", "shortest_name_length": 3}
{"curie": "MONDO:0015471", "names": ["Adolescent benign focal crisis", "adolescent benign focal crisis", "Benign focal seizure of adolescence", "Benign focal seizures of adolescence", "benign focal seizures of adolescence", "Benign focal seizure of adolescence (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign focal seizures of adolescence", "shortest_name_length": 30}
{"curie": "MONDO:0002507", "names": ["Gingival bulge", "GUM HYPERPLASIA", "Gum enlargement", "HYPERPLASIA GUM", "Hyperplasia gum", "Gum hyperplasia", "gum hyperplasia", "Gum hypertrophy", "gum; hyperplasia", "hyperplasia; gum", "gingival overgrowth", "Gingival overgrowth", "gingiva hyperplasia", "Gingival Overgrowth", "Gingival Overgrowths", "Overgrowth, Gingival", "GINGIVAL HYPERPLASIA", "enlargement gingival", "gingiva; hyperplasia", "Gingival enlargement", "thickening; gingival", "Gingival Hyperplasia", "gingival enlargement", "hyperplasia gingival", "hyperplasia; gingiva", "Hyperplastic gingiva", "gingival hyperplasia", "Gingival hyperplasia", "Overgrowths, Gingival", "Gingival Hyperplasias", "Hyperplasia, Gingival", "gingival; Enlargement", "Hyperplasias, Gingival", "Hyperplasia of gingiva", "Hyperplasia of gingivae", "Hypertrophic gingivitis", "Gingival enlargement NOS", "Gingival enlargement, NOS", "Oral soft tissue hyperplasia", "Gingival enlargement (disorder)", "gingival enlargement (diagnosis)", "Hyperplasia of gingiva (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gingival overgrowth", "shortest_name_length": 14}
{"curie": "MONDO:0004573", "names": ["RBFVD", "Ariboflavinosis", "ariboflavinosis", "ARIBOFLAVINOSIS", "deficiency riboflavin", "Riboflavin Deficiency", "riboflavin deficiency", "Vitamin B2 deficiency", "b2 deficiency vitamin", "vitamin B2 deficiency", "vitamin b2 deficiency", "VITAMIN B2 DEFICIENCY", "Riboflavin deficiency", "RIBOFLAVIN DEFICIENCY", "riboflavin; deficiency", "Riboflavine deficiency", "deficiency; riboflavin", "Deficiency, Riboflavin", "Riboflavin Deficiencies", "b2 deficiencies vitamin", "riboflavin deficiencies", "Deficiencies, Riboflavin", "Low levels of vitamin B2", "Ariboflavinosis (disorder)", "ariboflavinosis (diagnosis)", "Riboflavin deficiency disease", "riboflavin deficiency (diagnosis)", "deficiency; vitamin, B2 (riboflavin)", "vitamin; deficiency, B2 (riboflavin)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ariboflavinosis", "shortest_name_length": 5}
{"curie": "MONDO:0006814", "names": ["IRITIS", "iritis", "Iritis", "Iritides", "Iritis, NOS", "iritis (disease)", "Iris inflammation", "iris inflammation", "Iritis (disorder)", "iritis (diagnosis)", "iritis was observed", "Inflammation of iris", "inflammation of iris", "iritis (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "iritis", "shortest_name_length": 6}
{"curie": "MONDO:0009664", "names": ["MUL", "Mulibrey nanism", "Mulibrey Nanism", "mulibrey nanism", "MULIBREY NANISM", "Nanism, Mulibrey", "mulibrey dwarfism", "PERHEENTUPA SYNDROME", "Perheentupa syndrome", "Perheentupa Syndrome", "Syndrome, Perheentupa", "Mulibrey nanism syndrome", "Mulibrey growth disorder", "Mulibrey Nanism Syndrome", "Nanism Syndrome, Mulibrey", "Syndrome, Mulibrey Nanism", "Muscle-liver-brain-eye nanism", "MUSCLE-LIVER-BRAIN-EYE NANISM", "Muscle-Liver-Brain-Eye Nanism", "Muscle Liver Brain Eye Nanism", "muscle-liver-brain-eye nanism", "dwarfism-pericarditis syndrome", "Nanism, Muscle-Liver-Brain-Eye", "Mulibrey nanism syndrome (disorder)", "Muscle, liver, brain, eye nanism syndrome", "nanism-constrictive pericarditis syndrome", "pericardial constriction and Growth failure", "PERICARDIAL CONSTRICTION AND GROWTH FAILURE", "pericardial constriction and growth failure", "Pericardial Constriction And Growth Failure", "constrictive pericarditis-dwarfism syndrome", "Pericardial constriction with growth failure", "growth failure-pericardial constriction syndrome", "pericardial constriction-growth failure syndrome", "mulibrey (muscle-liver-brain-eye) nanism or dwarfism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mulibrey nanism", "shortest_name_length": 3}
{"curie": "MONDO:0015191", "names": ["myopathic intestinal pseudoobstruction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathic intestinal pseudoobstruction", "shortest_name_length": 38}
{"curie": "UMLS:C0267897", "names": ["GALLBLADDER RUPTURE", "gallbladder rupture", "Gallbladder rupture", "gallbladder; rupture", "rupture; gallbladder", "Gallbladder ruptured", "rupture of gallbladder", "Rupture of gallbladder", "of gallbladder rupture", "Disruption of gallbladder", "Rupture of gallbladder (disorder)", "rupture of gallbladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rupture of gallbladder", "shortest_name_length": 19}
{"curie": "MONDO:0015334", "names": ["branchial arch or oral-acral syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "branchial arch or oral-acral syndrome", "shortest_name_length": 37}
{"curie": "MONDO:0019178", "names": ["auricular abnormalities-cleft lip with or without cleft palate-ocular abnormalities syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "auricular abnormalities-cleft lip with or without cleft palate-ocular abnormalities syndrome", "shortest_name_length": 92}
{"curie": "MONDO:0021723", "names": ["vulvismus", "Vulvismus", "vaginismus", "VAGINISMUS", "Vaginismus", "colpospasm", "Colpospasm", "Vaginospasm", "vaginal spasm", "Vaginal spasm", "Pelvic floor myalgia", "Vaginospasm (finding)", "vulvismus (diagnosis)", "vaginismus (diagnosis)", "colpospasm (diagnosis)", "myalgia of pelvic floor", "Myalgia of pelvic floor", "Spasm of vaginal muscles at intercourse"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vaginismus", "shortest_name_length": 9}
{"curie": "UMLS:C0206636", "names": ["Chondromatoses", "Chondromatosis", "chondromatosis", "Chondromatosis NOS", "Chondromatosis, NOS", "Chondromatosis (disorder)", "Cartilage analog of fibromatosis", "Cartilage analogue of fibromatosis", "Chondromatosis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chondromatosis", "shortest_name_length": 14}
{"curie": "MONDO:0013022", "names": ["RLS7", "restless legs syndrome 7", "restless legs syndrome, susceptibility to, 7", "RESTLESS LEGS SYNDROME, SUSCEPTIBILITY TO, 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "restless legs syndrome, susceptibility to, 7", "shortest_name_length": 4}
{"curie": "MONDO:0013479", "names": ["CMD1HH", "dilated cardiomyopathy 1HH", "cardiomyopathy, dilated, 1HH", "CARDIOMYOPATHY, DILATED, 1HH", "dilated cardiomyopathy type 1HH", "cardiomyopathy, dilated, type 1Hh", "BAG3 familial isolated dilated cardiomyopathy", "familial isolated dilated cardiomyopathy caused by mutation in BAG3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1HH", "shortest_name_length": 6}
{"curie": "UMLS:C0524598", "names": ["Occult Fracture", "Occult fracture", "fracture occult", "occult fracture", "Occult Fractures", "fractures occult", "Fracture, Occult", "occult fractures", "Fractures, Occult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fractures, Occult", "shortest_name_length": 15}
{"curie": "MONDO:0002371", "names": ["Pericanalicular Fibroadenoma", "pericanalicular fibroadenoma", "Pericanalicular fibroadenoma", "pericanalicular breast fibroadenoma", "Pericanalicular Breast Fibroadenoma", "breast pericanalicular fibroadenoma", "Breast Pericanalicular Fibroadenoma", "Pericanalicular Fibroadenoma of breast", "pericanalicular fibroadenoma of breast", "Pericanalicular Fibroadenoma of Breast", "Pericanalicular Fibroadenoma of the Breast", "pericanalicular fibroadenoma of the breast", "pericanalicular; fibroadenoma, unspecified site", "fibroadenoma; pericanalicular, unspecified site", "Pericanalicular fibroadenoma (morphologic abnormality)", "pericanalicular fibroadenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast pericanalicular fibroadenoma", "shortest_name_length": 28}
{"curie": "MONDO:0005493", "names": ["carbon monoxide-induced delayed encephalopathy", "delayed encephalopathy after acute carbon monoxide poisoning"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carbon monoxide-induced delayed encephalopathy", "shortest_name_length": 46}
{"curie": "MONDO:0007284", "names": ["CTRCT20", "CRYGS cataract (disease)", "cataract 20 multiple types", "cataract 20, multiple types", "CATARACT 20, MULTIPLE TYPES", "cataract (disease) caused by mutation in CRYGS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 20 multiple types", "shortest_name_length": 7}
{"curie": "MONDO:0044768", "names": ["Vagal nerve tumors", "Vagal paraganglioma", "vagal paraganglioma", "Vagal nerve tumours", "Vagal Paraganglioma", "Glomus vagale tumor", "glomus vagale tumor", "Glomus vagale tumour", "vagal body paraganglioma", "Vagal Body Paraganglioma", "neoplasm of glomus vagale", "vagus nerve paraganglioma", "Vagus Nerve Paraganglioma", "Paraganglioma of Vagal Body", "Glomus vagale paraganglioma", "paraganglioma of vagal body", "Paraganglioma of Vagus Nerve", "paraganglioma of vagus nerve", "Glomus vagale tumor (disorder)", "Paraganglioma of the Vagal Body", "paraganglioma of the vagal body", "paraganglioma of the vagus nerve", "Paraganglioma of the Vagus Nerve", "Vagal nerve tumors (glomus vagale)", "neoplasm of glomus vagale (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vagus nerve paraganglioma", "shortest_name_length": 18}
{"curie": "UMLS:C1710498", "names": ["Type 3 DLBCL", "DLBCL Unclassifiable", "Type 3 Diffuse Large B-Cell Lymphoma", "Diffuse Large B-Cell Lymphoma Indeterminate", "Diffuse Large B-Cell Lymphoma Unclassifiable", "Diffuse large B-cell lymphoma, unclassifiable, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse large B-cell lymphoma, unclassifiable, NOS", "shortest_name_length": 12}
{"curie": "MONDO:0001497", "names": ["male genital organ vascular disease", "Male genital organ vascular diseases", "vascular disorder of male genital organs", "disorder of male genital organs vascular", "Vascular disorders of male genital organs", "Male genital organ vascular diseases (disorder)", "vascular disorder of male genital organs (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "male genital organ vascular disease", "shortest_name_length": 35}
{"curie": "MONDO:0009952", "names": ["Der Kaloustian McIntosh Silver syndrome", "Der Kaloustian-McIntosh-Silver syndrome", "Der Kaloustian Mcintosh Silver syndrome", "der Kaloustian mcintosh silver syndrome", "radioulnar synostosis-developmental delay-hypotonia syndrome", "Radioulnar synostosis-developmental delay-hypotonia syndrome", "radioulnar synostosis with developmental delay and hypotonia syndrome", "Radioulnar synostosis with developmental delay and hypotonia syndrome", "radioulnar synostosis, unilateral, with developmental retardation and hypotonia", "RADIOULNAR SYNOSTOSIS, UNILATERAL, WITH DEVELOPMENTAL RETARDATION AND HYPOTONIA", "Radioulnar Synostosis, Unilateral, with Developmental Retardation and Hypotonia", "Radioulnar synostosis with developmental delay and hypotonia syndrome (disorder)", "radioulnar synostosis with developmental delay and hypotonia syndrome (diagnosis)", "radioulnar synostosis, unilateral, with developintellectual disability and hypotonia", "unilateral radio-ulnar synostosis, generalized hypotonia, developmental retardation, and a characteristic facial appearance", "unilateral radio-ulnar synostosis, generalized hypotonia, developintellectual disability, and a characteristic facial appearance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radioulnar synostosis-developmental delay-hypotonia syndrome", "shortest_name_length": 39}
{"curie": "MONDO:0000192", "names": ["polyglucosan body myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyglucosan body myopathy", "shortest_name_length": 26}
{"curie": "MONDO:0800113", "names": ["systemic vasculitis", "Vasculitis necrotizing", "necrotizing vasculitis", "necrotising vasculitis", "Vasculitis necrotising", "VASCULITIS NECROTIZING", "Necrotizing Vasculitis", "Necrotizing vasculitis", "vasculitis necrotizing", "Necrotising vasculitis", "Necrotizing vasculitis, NOS", "Systemic necrotising vasculitis", "Systemic necrotizing vasculitis", "systemic necrotizing vasculitis", "Necrotizing vasculitis (disorder)", "necrotizing vasculitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "necrotizing vasculitis", "shortest_name_length": 19}
{"curie": "MONDO:0003665", "names": ["Cervix Endometrioid Carcinoma", "cervix endometrioid carcinoma", "cervical endometrioid carcinoma", "Cervical Endometrioid Carcinoma", "Endometrioid Carcinoma of Cervix", "endometrioid carcinoma of cervix", "Cervix Endometrioid Adenocarcinoma", "cervix endometrioid adenocarcinoma", "cervix uteri endometrioid carcinoma", "Cervix Uteri Endometrioid Carcinoma", "cervical endometrioid adenocarcinoma", "Cervical Endometrioid Adenocarcinoma", "endometrioid carcinoma of the cervix", "Endometrioid Carcinoma of the Cervix", "Uterine Cervix Endometrioid Carcinoma", "uterine cervix endometrioid carcinoma", "endometrioid adenocarcinoma of cervix", "Endometrioid Adenocarcinoma of Cervix", "endometrioid carcinoma of cervix uteri", "Endometrioid Carcinoma of Cervix Uteri", "cervix uteri endometrioid adenocarcinoma", "endometrioid carcinoma of uterine cervix", "Cervix Uteri Endometrioid Adenocarcinoma", "Endometrioid Carcinoma of Uterine Cervix", "endometrioid adenocarcinoma of the cervix", "Endometrioid Adenocarcinoma of the Cervix", "Uterine Cervix Endometrioid Adenocarcinoma", "endometrioid carcinoma of the Cervix Uteri", "endometrioid carcinoma of the cervix uteri", "Endometrioid Carcinoma of the Cervix Uteri", "uterine cervix endometrioid adenocarcinoma", "Endometrioid Adenocarcinoma of Cervix Uteri", "endometrioid adenocarcinoma of cervix uteri", "endometrioid carcinoma of the uterine cervix", "Endometrioid Carcinoma of the Uterine Cervix", "endometrioid adenocarcinoma of uterine cervix", "Endometrioid Adenocarcinoma of Uterine Cervix", "endometrioid adenocarcinoma of the cervix uteri", "Endometrioid Adenocarcinoma of the Cervix Uteri", "Endometrioid Adenocarcinoma of the Uterine Cervix", "endometrioid adenocarcinoma of the uterine cervix"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical endometrioid adenocarcinoma", "shortest_name_length": 29}
{"curie": "UMLS:C4721657", "names": ["Stage I Ovarian Teratoma", "Stage I Ovarian Teratoma AJCC v6", "Stage I Ovarian Teratoma AJCC v7", "Stage I Ovarian Germ Cell Teratoma", "Stage I Ovarian Teratoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Ovarian Teratoma AJCC v6 and v7", "shortest_name_length": 24}
{"curie": "UMLS:C1167792", "names": ["Bacterial pyelonephritis", "Bacterial pyelonephritis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bacterial pyelonephritis", "shortest_name_length": 24}
{"curie": "MONDO:0000240", "names": ["Invasive aspergillosis", "invasive aspergillosis", "aspergillosis invasive", "ASPERGILLOSIS, INVASIVE", "Invasive aspergillosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "invasive aspergillosis", "shortest_name_length": 22}
{"curie": "MONDO:0019576", "names": ["Paucicellular mastocytosis", "Telangiectatic cutaneous mastocytosis", "Telangiectasia macularis eruptive perstans", "Telangiectasia macularis eruptiva perstans", "telangiectasia macularis eruptiva perstans", "TMEP - telangiectasia macularis eruptiva perstans", "Telangiectasia macularis eruptiva perstans (disorder)", "telangiectasia macularis eruptiva perstans (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "telangiectasia macularis eruptiva perstans", "shortest_name_length": 26}
{"curie": "MONDO:0021424", "names": ["skin hemangiopericytoma", "Skin Hemangiopericytoma", "Hemangiopericytoma of Skin", "Hemangiopericytoma of skin", "hemangiopericytoma of skin", "Haemangiopericytoma of skin", "hemangiopericytoma of the skin", "Hemangiopericytoma of the Skin", "zone of skin hemangiopericytoma", "Hemangiopericytoma of skin (disorder)", "Hemangiopericytoma of skin (diagnosis)", "neoplasm - blood vessels of skin hemangiopericytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemangiopericytoma of skin", "shortest_name_length": 23}
{"curie": "MONDO:0014286", "names": ["HSN1F", "HSN 1F", "HSN IF", "hereditary sensory neuropathy type IF", "hereditary sensory neuropathy type 1F", "neuropathy, hereditary sensory, type IF", "neuropathy, hereditary sensory, type 1F", "NEUROPATHY, HEREDITARY SENSORY, TYPE IF", "ATL3 hereditary sensory and autonomic neuropathy type 1", "hereditary sensory and autonomic neuropathy type 1 caused by mutation in ATL3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuropathy, hereditary sensory, type 1F", "shortest_name_length": 5}
{"curie": "MONDO:0007956", "names": ["Pai syndrome", "PAI SYNDROME", "Pai Levkoff syndrome", "Median cleft lip, corpus callosum, lipoma, and skin polyps", "median cleft of upper lip with polyps of facial skin and nasal mucosa", "CLEFT, MEDIAN, OF UPPER LIP WITH POLYPS OF FACIAL SKIN AND NASAL MUCOSA", "Cleft, median, of upper lip with polyps of facial skin and nasal mucosa", "cleft, Median, of upper lip with polyps of Facial skin and nasal mucosa", "cleft, MEDIAN, of upper LIP with polyps of facial skin and nasal mucosa", "Median cleft of upper lip, corpus callosum lipoma, cutaneous polyp syndrome", "median cleft of the upper lip-corpus callosum lipoma-cutaneous polyps syndrome", "Median cleft of upper lip, corpus callosum lipoma, cutaneous polyp syndrome (disorder)", "Median cleft of the upper lip-corpus callosum lipoma-midline facial cutaneous polyps syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pai syndrome", "shortest_name_length": 12}
{"curie": "UMLS:C4527184", "names": ["Stage III Cutaneous (Skin) Melanoma", "Pathologic Stage III Cutaneous Melanoma AJCC v8", "Pathologic Stage III Melanoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage III Cutaneous Melanoma AJCC v8", "shortest_name_length": 35}
{"curie": "UMLS:C1328519", "names": ["Retinal pigment epithelial tear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retinal pigment epithelial tear", "shortest_name_length": 31}
{"curie": "UMLS:C5446572", "names": ["Conjunctival Myxoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conjunctival Myxoma", "shortest_name_length": 19}
{"curie": "MONDO:0015375", "names": ["OFD", "Orofaciodigital syndrome", "Orofaciodigital Syndrome", "orofaciodigital syndrome", "Dysplasia Linguofacialis", "Orodigitofacial Syndrome", "Orofaciodigital Syndromes", "orofaciodigital syndromes", "Syndrome, Orofaciodigital", "Oro-Facio-Digital Syndrome", "orofacial-digital syndrome", "orofacial digital syndrome", "Orodigitofacial Dysostosis", "Syndromes, Orofaciodigital", "Orodigitofacial dysostosis", "Orofacial-digital syndrome", "Oro-facial-digital syndrome", "Oral-Facial-Digital Syndrome", "oro-facial-digital; syndrome", "oral-facial-digital syndrome", "Oral-facial-digital syndrome", "oral facial digital syndrome", "syndrome; oro-facial-digital", "oral-facial-digital syndromes", "oral facial digital syndromes", "Oral-facial-digital syndrome (disorder)", "oral-facial-digital syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orofaciodigital syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0006462", "names": ["Thyroid Diffuse Large B-Cell Lymphoma", "thyroid diffuse large B-cell lymphoma", "Diffuse Large B-Cell Lymphoma of Thyroid", "diffuse large B-cell lymphoma of thyroid", "thyroid gland diffuse large B-cell lymphoma", "Thyroid Gland Diffuse Large B-Cell Lymphoma", "diffuse large B-cell lymphoma of the thyroid", "Diffuse Large B-Cell Lymphoma of the Thyroid", "diffuse large B-cell lymphoma of thyroid gland", "Diffuse Large B-Cell Lymphoma of Thyroid Gland", "large B-cell diffuse lymphoma of thyroid gland", "Diffuse Large B-Cell Lymphoma of the Thyroid Gland", "diffuse large B-cell lymphoma of the thyroid gland", "Primary Thyroid Gland Diffuse Large B-Cell Lymphoma", "primary thyroid gland diffuse large B-cell lymphoma", "large B-cell diffuse lymphoma of thyroid gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid gland diffuse large B-cell lymphoma", "shortest_name_length": 37}
{"curie": "UMLS:C1708537", "names": ["Intermediate (Locally Aggressive) Blood Vessel Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intermediate (Locally Aggressive) Blood Vessel Neoplasm", "shortest_name_length": 55}
{"curie": "UMLS:C1336166", "names": ["Nasopharyngeal Keratinizing Squamous Cell Carcinoma Stage IIA", "Stage IIA Nasopharyngeal Keratinizing Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Nasopharyngeal Keratinizing Squamous Cell Carcinoma", "shortest_name_length": 61}
{"curie": "UMLS:C0028797", "names": ["occupational disease", "Occupational Disease", "Occupational diseases", "diseases occupational", "Disease, Occupational", "Occupational disorder", "Occupational Diseases", "occupational disorder", "occupational diseases", "Occupational Illnesse", "Diseases, Occupational", "Illnesse, Occupational", "disorders occupational", "Occupational Illnesses", "Illnesses, Occupational", "occupational disease/disorder", "Occupational disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Occupational Diseases", "shortest_name_length": 20}
{"curie": "UMLS:C0162669", "names": ["Pleoconial myopathy", "Pleoconial Myopathy", "Myopathy, Pleoconial", "Pleoconial Myopathies", "Myopathies, Pleoconial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pleoconial Myopathies", "shortest_name_length": 19}
{"curie": "MONDO:0014269", "names": ["COXPD19", "combined oxidative phosphorylation deficiency 19", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 19", "LYRM4 combined oxidative phosphorylation deficiency", "combined oxidative phosphorylation deficiency type 19", "severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency", "combined oxidative phosphorylation deficiency caused by mutation in LYRM4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation deficiency 19", "shortest_name_length": 7}
{"curie": "UMLS:C5237271", "names": ["Locally Advanced Lip and Oral Cavity Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Lip and Oral Cavity Carcinoma", "shortest_name_length": 46}
{"curie": "MONDO:0021505", "names": ["Benign Endocardial Tumor", "benign endocardial tumor", "endocardium benign neoplasm", "Benign Endocardial Neoplasm", "Benign Tumor of Endocardium", "Benign tumor of endocardium", "benign endocardial neoplasm", "benign tumor of endocardium", "Benign tumour of endocardium", "benign neoplasm of endocardium", "Benign Neoplasm of Endocardium", "Benign neoplasm of endocardium", "benign tumor of the endocardium", "Benign Tumor of the Endocardium", "Benign Neoplasm of the Endocardium", "benign neoplasm of the endocardium", "Benign neoplasm of endocardium (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of endocardium", "shortest_name_length": 24}
{"curie": "MONDO:0016241", "names": ["AHC", "alternating hemiplegia", "Alternating hemiplegia", "adrenal hypoplasia congenita", "Adrenal Hypoplasia Congenita", "congenital adrenal Hypoplasia", "Congenital Adrenal Hypoplasia", "alternating hemiplegia syndrome", "Alternating hemiplegia syndrome", "childhood alternating hemiplegia", "alternating childhood hemiplegia", "pediatric alternating hemiplegia", "alternating hemiplegia childhood", "Alternating hemiplegia of childhood", "congenital adrenal gland hypoplasia", "Congenital Adrenal Gland Hypoplasia", "alternating hemiplegia of childhood", "Alternating hemiplegia of childhood (disorder)", "alternating hemiplegia of childhood (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alternating hemiplegia of childhood", "shortest_name_length": 3}
{"curie": "MONDO:0001888", "names": ["anus lymphoma", "Anal Lymphoma", "anal lymphoma", "Lymphoma of anus", "Lymphoma of Anus", "lymphoma of anus", "Lymphoma of the Anus", "lymphoma of the anus", "Primary Anal Lymphoma", "primary anal lymphoma", "Lymphoma of anus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anus lymphoma", "shortest_name_length": 13}
{"curie": "UMLS:C4744391", "names": ["Sellar Teratoma", "Teratoma of the Sellar Region"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sellar Teratoma", "shortest_name_length": 15}
{"curie": "MONDO:0014462", "names": ["FSGS8", "FOCAL SEGMENTAL GLOMERULOSCLEROSIS 8", "focal segmental glomerulosclerosis 8", "GLOMERULOSCLEROSIS, FOCAL SEGMENTAL, 8", "glomerulosclerosis, focal segmental, 8", "ANLN focal segmental glomerulosclerosis", "focal segmental glomerulosclerosis type 8", "focal segmental glomerulosclerosis caused by mutation in ANLN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal segmental glomerulosclerosis 8", "shortest_name_length": 5}
{"curie": "UMLS:C1336715", "names": ["testicular seminoma and embryonal carcinoma", "testicular embryonal carcinoma and seminoma", "embryonal carcinoma and seminoma, testicular", "seminoma and embryonal carcinoma of the testis", "testis cancer, seminoma and embryonal carcinoma", "testis cancer, embryonal carcinoma and seminoma", "Mixed Embryonal Carcinoma and Seminoma of Testis", "Testicular Mixed Embryonal Carcinoma and Seminoma", "testicle cancer, embryonal carcinoma and seminoma", "testicular cancer, seminoma and embryonal carcinoma", "testicular cancer, embryonal carcinoma and seminoma", "Mixed Embryonal Carcinoma and Seminoma of the Testis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular Mixed Embryonal Carcinoma and Seminoma", "shortest_name_length": 43}
{"curie": "MONDO:0018748", "names": ["linear iga", "Linear IgA", "linear iga disease", "Linear IgA disease", "Linear Ig A disease", "Linear IgA Dermatoses", "linear IgA Dermatosis", "linear IgA dermatosis", "Linear IgA dermatosis", "linear iga dermatosis", "dermatosis iga linear", "Linear IgA Dermatosis", "Dermatosis, Linear IgA", "IgA Dermatoses, Linear", "IgA Dermatosis, Linear", "Dermatoses, Linear IgA", "LAD - Linear IgA disease", "linear iga bullous dermatosis", "Linear IgA Bullous Dermatosis", "Linear IgA bullous dermatosis", "linear IgA dermatosis (diagnosis)", "Linear immunoglobulin A dermatosis", "Linear immunoglobulin A bullous dermatosis", "Linear immunoglobulin A dermatosis (disorder)", "IgA - Linear immunoglobulin A bullous dermatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "linear IgA Dermatosis", "shortest_name_length": 10}
{"curie": "MONDO:0007807", "names": ["HYPOXANTHINE GUANINE PHOSPHORIBOSYLTRANSFERASE SUPPRESSOR", "hypoxanthine guanine phosphoribosyltransferase suppressor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypoxanthine guanine phosphoribosyltransferase suppressor", "shortest_name_length": 57}
{"curie": "UMLS:C0085693", "names": ["acute appendicitis", "Appendicitis;acute", "appendicitis acute", "Acute appendicitis", "APPENDICITIS ACUTE", "Acute Appendicitis", "appendicitis; acute", "APPENDICITIS, ACUTE", "acute; appendicitis", "Acute appendicitis NOS", "Acute appendicitis, NOS", "acute inflamed appendicitis", "inflamed acute appendicitis", "Acute appendicitis (disorder)", "acute appendicitis (diagnosis)", "Unspecified acute appendicitis", "Acute appendicitis, unspecified", "Acute appendicitis NOS (disorder)", "acute inflamed appendicitis (diagnosis)", "Acute appendicitis; not otherwise specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute appendicitis NOS (disorder)", "shortest_name_length": 18}
{"curie": "MONDO:0043193", "names": ["Richieri Costa Guion-Almeida syndrome", "Richieri Costa Guion-Almeida dwarfism", "Richieri-costa Guion-Almeida Cohen syndrome", "richieri-costa guion-almeida cohen syndrome", "Richieri-Costa Guion-Almeida Cohen syndrome", "overgrowth - craniosynostosis - arthrogryposis", "acrofacial dysostosis Richieri Costa Guion-Almeida type", "Acrofacial dysostosis Richieri Costa Guion-Almeida type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "richieri-costa guion-almeida cohen syndrome", "shortest_name_length": 37}
{"curie": "MONDO:0016338", "names": ["non-familial dilated cardiomyopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-familial dilated cardiomyopathy", "shortest_name_length": 35}
{"curie": "MONDO:0003541", "names": ["Adult ALL", "adult ALL", "ALL, adult", "Adult Acute Lymphoid Leukemia", "adult acute lymphoid Leukemia", "adult acute lymphoid leukemia", "adult acute lymphocytic leukemia", "Adult Acute Lymphocytic Leukemia", "Adult Acute Lymphogenous Leukemia", "adult acute lymphogenous leukemia", "adult acute lymphoblastic leukemia", "Acute Lymphoblastic Leukemia (ALL)", "Adult Acute Lymphoblastic Leukemia", "acute lymphoblastic leukemia (ALL)", "acute lymphoblastic leukemia, adult", "adult leukemia, acute lymphoblastic", "lymphoblastic leukemia, acute adult", "leukemia, acute lymphoblastic, adult", "adult precursor lymphoblastic leukemia", "Adult Precursor Lymphoblastic Leukemia", "Leukemia, acute lymphocytic (ALL), adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult acute lymphoblastic leukemia", "shortest_name_length": 9}
{"curie": "MONDO:0014218", "names": ["EPKHE", "SAM SYNDROME", "SAM syndrome", "Sam syndrome", "Severe dermatitis-multiple allergies-metabolic wasting syndrome", "severe dermatitis-multiple allergies-metabolic wasting syndrome", "Severe dermatitis, multiple allergies, metabolic wasting syndrome", "severe dermatitis, multiple allergies, and metabolic wasting syndrome", "SEVERE DERMATITIS, MULTIPLE ALLERGIES, AND METABOLIC WASTING SYNDROME", "Severe dermatitis, multiple allergies, metabolic wasting syndrome (disorder)", "ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IgE", "erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-IgE", "erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper IgE", "Congenital erythroderma-hypotrichosis-recurrent infections-multiple food allergies syndrome", "congenital erythroderma-hypotrichosis-recurrent infections-multiple food allergies syndrome", "Congenital erythroderma, hypotrichosis, recurrent infections, multiple food allergies syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe dermatitis-multiple allergies-metabolic wasting syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0016564", "names": ["PSP-AOS", "PSP-PNFA", "progressive supranuclear palsy-apraxia of speech syndrome", "progressive supranuclear palsy-progressive non-fluent aphasia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive supranuclear palsy-progressive non-fluent aphasia syndrome", "shortest_name_length": 7}
{"curie": "MONDO:0001660", "names": ["PDR", "Proliferative diabetic retinopathy", "proliferative diabetic retinopathy", "Proliferative Diabetic Retinopathy", "DIABETIC RETINOPATHY PROLIFERATIVE", "PDR - Proliferative diabetic retinopathy", "proliferative diabetic retinopathy (PDR)", "PDR - proliferative diabetic retinopathy", "Proliferative retinopathy with diabetes mellitus", "diabetes with proliferative diabetic retinopathy", "Proliferative retinopathy due to diabetes mellitus", "diabetes with proliferative diabetic retinopathy (diagnosis)", "Proliferative retinopathy due to diabetes mellitus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "proliferative diabetic retinopathy", "shortest_name_length": 3}
{"curie": "UMLS:C5419517", "names": ["Locally Advanced Unclassified Renal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Unclassified Renal Cell Carcinoma", "shortest_name_length": 50}
{"curie": "UMLS:C1335730", "names": ["Refractory Nodular Lymphocyte Predominant Hodgkin Lymphoma", "Refractory Nodular Lymphocyte Predominant Hodgkin's Disease", "Refractory Nodular Lymphocyte Predominant Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Nodular Lymphocyte Predominant Hodgkin Lymphoma", "shortest_name_length": 58}
{"curie": "MONDO:0054637", "names": ["NSLH", "NSLH1", "TOSTI SYNDROME", "Tosti syndrome", "Tosti Syndrome", "Mazzanti Syndrome", "MAZZANTI SYNDROME", "Noonan syndrome-like with loose anagen hair 1", "NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1", "Noonan syndrome-like disorder with loose anagen hair 1", "Noonan Syndrome-Like Disorder with Loose Anagen Hair 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Noonan syndrome-like disorder with loose anagen hair 1", "shortest_name_length": 4}
{"curie": "MONDO:0018439", "names": ["Colonic eosinophilia", "Eosinophilic Colitis", "Eosinophilic colitis", "colitis eosinophilic", "eosinophilic colitis", "Eosinophilic colitis (disorder)", "eosinophilic colitis (diagnosis)", "Eosinophilic infiltration in the colon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eosinophilic colitis", "shortest_name_length": 20}
{"curie": "UMLS:C4727197", "names": ["Soft Tissue Sarcoma, Excluding Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Soft Tissue Sarcoma, Excluding Liposarcoma", "shortest_name_length": 42}
{"curie": "UMLS:C0339223", "names": ["Neuroparalytic keratitis", "corneal ulcer neuropathic", "Neuropathic corneal ulcer", "Neurotrophic corneal ulcer", "Neuropathic corneal ulcer (disorder)", "Neuropathic corneal ulcer (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neuropathic corneal ulcer", "shortest_name_length": 24}
{"curie": "MONDO:0008560", "names": ["THPH2", "apc resistance", "APC RESISTANCE", "APC resistance", "APC Resistance", "Resistance, APC", "Thrombophilia V", "thrombophilia V", "Pccf deficiency", "thrombophilia 5", "PCCF deficiency", "PCCF DEFICIENCY", "resistance, APC", "THROMBOPHILIA V", "Proc cofactor deficiency", "PROC COFACTOR DEFICIENCY", "PROC cofactor deficiency", "Apc Resistance, Leiden Type", "Factor V Leiden thrombophilia", "Factor V Leiden Thrombophilia", "Protein C Cofactor Deficiency", "ACTIVATED PROTEIN C RESISTANCE", "Activated protein C resistance", "activated protein c resistance", "activated protein C resistance", "Activated Protein C resistance", "Activated Protein C Resistance", "Resistance to activated protein C", "THROMBOPHILIA DUE TO FACTOR V LEIDEN", "Thrombophilia due to Factor V Leiden", "thrombophilia due to Factor 5 Leiden", "activated protein C resistance (diagnosis)", "Hereditary Resistance To Activated Protein C", "THROMBOPHILIA DUE TO ACTIVATED PROTEIN C RESISTANCE", "Thrombophilia due to Activated Protein C Resistance", "thrombophilia due to ACTIVATED PROTEIN C resistance", "thrombophilia due to activated protein C resistance", "thrombophilia 2 due to activated protein C resistance", "Resistance to activated protein C due to Factor V R506Q", "Resistance to activated protein C due to Factor V Leiden", "thrombophilia, susceptibility to, due to factor V Leiden", "Resistance to activated protein C caused by Factor V R506Q", "Resistance to activated protein C caused by Factor V Leiden", "THROMBOPHILIA DUE TO ACTIVATED PROTEIN C RESISTANCE (disorder)", "Thrombophilia due to Deficiency of Activated Protein C Cofactor", "thrombophilia due to deficiency of Activated Protein C cofactor", "thrombophilia due to deficiency of activated protein C cofactor", "THROMBOPHILIA DUE TO DEFICIENCY OF ACTIVATED PROTEIN C COFACTOR", "Resistance to activated protein C caused by Factor V Leiden (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombophilia due to activated protein C resistance", "shortest_name_length": 5}
{"curie": "MONDO:0100237", "names": ["inherited cutis laxa", "hereditary cutis laxa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited cutis laxa", "shortest_name_length": 20}
{"curie": "UMLS:C0855221", "names": ["Jealous delusion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jealous delusion", "shortest_name_length": 16}
{"curie": "UMLS:C4055622", "names": ["A2/3 Hydronephrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "A2/3 Hydronephrosis", "shortest_name_length": 19}
{"curie": "UMLS:C4683423", "names": ["I Under 55 Years", "Stage I Thyroid Gland Papillary Cancer Under 55 Years", "Stage I Thyroid Gland Papillary Carcinoma Under 55 Years AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Thyroid Gland Papillary Carcinoma Under 55 Years AJCC v8", "shortest_name_length": 16}
{"curie": "MONDO:0006201", "names": ["ethmoid sinus adenoid cystic carcinoma", "Ethmoid Sinus Adenoid Cystic Carcinoma", "Adenoid Cystic Carcinoma of Ethmoid Sinus", "adenoid cystic carcinoma of ethmoid sinus", "Adenoid Cystic Carcinoma of the Ethmoid Sinus", "adenoid cystic carcinoma of the ethmoid sinus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ethmoid sinus adenoid cystic carcinoma", "shortest_name_length": 38}
{"curie": "MONDO:0022034", "names": ["Lentivirus disease", "lentivirus infection", "Lentivirus Infection", "Infection, Lentivirus", "Lentivirus Infections", "Lentivirus infections", "Infections, Lentivirus", "Disease due to Lentivirus", "Disease caused by Lentivirus", "Disease due to Lentivirus, NOS", "Disease caused by Lentivirus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lentivirus infection", "shortest_name_length": 18}
{"curie": "UMLS:C0338630", "names": ["Senile Paranoid Dementia", "Senile dementia, paranoid", "Paranoid Dementia, Senile", "Senile Paranoid Dementias", "Dementias, Senile Paranoid", "Paranoid Dementias, Senile", "Senile dementia with paranoia", "senile dementia with paranoia", "Senile dementia with paranoia (disorder)", "senile dementia with paranoia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Senile Paranoid Dementia", "shortest_name_length": 24}
{"curie": "UMLS:C5554611", "names": ["Ovarian Teratoma with Malignant Transformation", "Ovarian Dermoid Cyst with Somatic-Type Malignancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Dermoid Cyst with Somatic-Type Malignancy", "shortest_name_length": 46}
{"curie": "MONDO:0020385", "names": ["TGA with coarctation", "congenitally uncorrected transposition of the great vessels with coarctation", "congenitally uncorrected transposition of the great arteries with coarctation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenitally uncorrected transposition of the great arteries with coarctation", "shortest_name_length": 20}
{"curie": "MONDO:0009453", "names": ["Immune Deficiency Disease", "IMMUNE DEFICIENCY DISEASE", "immune deficiency disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immune deficiency disease", "shortest_name_length": 25}
{"curie": "UMLS:C3805052", "names": ["Splenic thrombosis", "Splenic Thrombosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Splenic thrombosis", "shortest_name_length": 18}
{"curie": "MONDO:0000224", "names": ["carbohydrate metabolism disease", "acquired carbohydrate metabolism disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired carbohydrate metabolism disease", "shortest_name_length": 31}
{"curie": "MONDO:0800181", "names": ["OPA1-related optic atrophy with or without extraocular features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "OPA1-related optic atrophy with or without extraocular features", "shortest_name_length": 63}
{"curie": "UMLS:C0269199", "names": ["stenosis cervix", "cervix stenosis", "stenosis; cervix", "Cervix stricture", "cervix; stenosis", "stenosis cervical", "cervical stenosis", "stricture; cervix", "CERVICAL STENOSIS", "cervix; stricture", "CERVICAL STRICTURE", "Stenosis of cervix", "stenosis of cervix", "Cervical stricture", "cervical stricture", "Stricture of cervix", "stricture of cervix", "Stricture of Cervical Os", "UTERINE CERVIX, STRICTURE", "Stenosis of cervix (disorder)", "cervical stenosis or stricture", "cervical stenosis or stricture (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stenosis of cervix", "shortest_name_length": 15}
{"curie": "MONDO:0014590", "names": ["CMS18", "congenital myasthenic syndrome 18", "MYASTHENIC SYNDROME, CONGENITAL, 18", "myasthenic syndrome, congenital, 18", "SNAP25 congenital myasthenic syndrome", "congenital myasthenic syndrome type 18", "myasthenic syndrome, congenital, type 18", "congenital myasthenic syndrome caused by mutation in SNAP25", "myasthenic syndrome, congenital, 18, with intellectual disability and ataxia", "MYASTHENIC SYNDROME, CONGENITAL, 18, WITH INTELLECTUAL DISABILITY AND ATAXIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myasthenic syndrome 18", "shortest_name_length": 5}
{"curie": "MONDO:0000510", "names": ["synucleinopathy", "Synucleinopathy", "synucleinopathies", "a-Synucleinopathy", "Synucleinopathies", "a-Synucleinopathies", "alpha-Synucleinopathy", "Alpha synucleinopathy", "alpha-Synucleinopathies", "alpha Synucleinopathies", "alpha synucleinopathies", "alpha Synuclein Pathology", "Alpha synuclein pathology", "Synucleinopathy (disorder)", "alpha Synuclein Pathologies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "synucleinopathy", "shortest_name_length": 15}
{"curie": "MONDO:0015741", "names": ["trisomy 18qter", "distal trisomy 18q", "distal duplication 18q", "distal trisomy type 18q", "telomeric duplication 18q"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal trisomy 18q", "shortest_name_length": 14}
{"curie": "UMLS:C4087471", "names": ["Cholangiocarcinoma metastatic", "Metastatic Cholangiocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cholangiocarcinoma metastatic", "shortest_name_length": 29}
{"curie": "UMLS:C1334217", "names": ["Intermediate Lipomatous Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intermediate Lipomatous Neoplasm", "shortest_name_length": 32}
{"curie": "MONDO:0019919", "names": ["UPD(22)mat", "maternal uniparental disomy of chromosome 22", "maternal uniparental disomy of chromosome type 22"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maternal uniparental disomy of chromosome 22", "shortest_name_length": 10}
{"curie": "MONDO:0017401", "names": ["familial isolated arrhythmogenic ventricular dysplasia, left dominant form", "familial isolated arrhythmogenic ventricular cardiomyopathy, left dominant form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial isolated arrhythmogenic ventricular dysplasia, left dominant form", "shortest_name_length": 74}
{"curie": "MONDO:0009480", "names": ["CORS", "JS-OR", "JS type B", "Arima syndrome", "ARIMA SYNDROME", "Joubert syndrome 5", "DEKABAN-ARIMA SYNDROME", "Dekaban-Arima Syndrome", "Dekaban-Arima syndrome", "Dekaban Arima syndrome", "Cerebellooculorenal syndrome", "Cerebello-oculo-renal syndrome", "cerebello-oculo-renal syndrome", "cerebrooculohepatorenal syndrome", "CEREBROOCULOHEPATORENAL SYNDROME", "Cerebro-oculo-hepato-renal syndrome", "cerebro-oculo-hepato-renal syndrome", "Joubert syndrome with oculorenal defect", "Joubert syndrome with oculorenal anomalies", "Joubert syndrome with Senior-Loken syndrome", "Joubert syndrome with oculorenal defect (disorder)", "chorioretinal coloboma with cerebellar vermis aplasia", "Chorioretinal coloboma with cerebellar vermis aplasia", "JOUBERT SYNDROME WITH BILATERAL CHORIORETINAL COLOBOMA", "Joubert syndrome with bilateral chorioretinal coloboma", "Coloboma, Chorioretinal, With Cerebellar Vermis Aplasia", "coloboma, chorioretinal, with cerebellar vermis aplasia", "COLOBOMA, CHORIORETINAL, WITH CEREBELLAR VERMIS APLASIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome with oculorenal defect", "shortest_name_length": 4}
{"curie": "MONDO:0018479", "names": ["CAH", "lipoid CAH", "adrenal hyperplasia", "Adrenal Hyperplasia", "adrenal hyperplasia 1", "adrenogenital disorder", "Adrenogenital Syndrome", "Adrenogenital Disorder", "adrenogenital syndrome", "Adrenogenital disorder", "adrenogenital disorders", "adrenogenital; disorder", "Adrenogenital disorders", "hyperplasia adrenal congenital", "Congenital Adrenal Hyperplasia", "CONGENITAL ADRENAL HYPERPLASIA", "adrenal congenital hyperplasia", "hyperplasia congenital adrenal", "ADRENAL HYPERPLASIA CONGENITAL", "Congenital adrenal hyperplasia", "congenital adrenal hyperplasia", "Hyperplasia, Congenital Adrenal", "ADRENAL HYPERPLASIA, CONGENITAL", "Adrenal Hyperplasia, Congenital", "Congenital Adrenal Hyperplasias", "adrenal hyperplasia, congenital", "Hyperplasias, Congenital Adrenal", "adrenal; hyperplasia, congenital", "Adrenal Hyperplasias, Congenital", "hyperplasia; adrenal, congenital", "Congenital adrenogenital syndrome", "Adrenogenital disorder (disorder)", "Adrenogenital disorder, unspecified", "Congenital adrenal hyperplasia, NOS", "adrenogenital disorders (diagnosis)", "CAH - Congenital adrenal hyperplasia", "disease (or disorder); adrenogenital", "Congenital Adrenal Gland Hyperplasia", "congenital adrenal gland hyperplasia", "congenital lipoid adrenal hyperplasia", "Adrenal hyperplasia syndrome, congenital", "Congenital adrenal hyperplasia (disorder)", "congenital adrenal hyperplasia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital adrenal hyperplasia", "shortest_name_length": 3}
{"curie": "MONDO:0016461", "names": ["dup(5)(q35)", "Dup(5)(q35)", "Trisomy 5q35", "trisomy 5q35", "5q35 microduplication syndrome", "5q35 microduplication syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "5q35 microduplication syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0020215", "names": ["syndromic corneal dystrophy", "syndromic corneal dystrophy (disease)", "syndrome associated with corneal dystrophy (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic corneal dystrophy", "shortest_name_length": 27}
{"curie": "MONDO:0014495", "names": ["RDJCSS", "retinal dystrophy-juvenile cataract-short stature syndrome", "Retinal dystrophy-juvenile cataract-short stature syndrome", "Retinal dystrophy, juvenile cataract, short stature syndrome", "RETINAL DYSTROPHY, JUVENILE CATARACTS, AND SHORT STATURE SYNDROME", "retinal dystrophy, juvenile cataracts, and short stature syndrome", "retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome", "Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome", "Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome", "Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C1336259", "names": ["Stage III Mouth Carcinoma", "Stage III Carcinoma of Mouth", "Stage III Oral Cavity Cancer", "Stage III Oral Cavity Carcinoma", "Stage III Carcinoma of the Mouth", "Stage III Carcinoma of Oral Cavity", "Stage III Oral Cavity Cancer AJCC v6", "Stage III Oral Cavity Cancer AJCC v7", "Stage III Carcinoma of the Oral Cavity", "Stage III Oral Cavity Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Oral Cavity Cancer AJCC v6 and v7", "shortest_name_length": 25}
{"curie": "MONDO:0017786", "names": ["dup(2)(q23.1)", "Dup(2)(q23.1)", "trisomy 2q23.1", "Trisomy 2q23.1", "2q23.1 microduplication syndrome", "2q23.1 microduplication syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "2q23.1 microduplication syndrome", "shortest_name_length": 13}
{"curie": "UMLS:C5420071", "names": ["Unresectable Esophageal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Esophageal Adenocarcinoma", "shortest_name_length": 38}
{"curie": "MONDO:0018394", "names": ["male infertility teratozoospermia due to single gene mutation", "male infertility with teratozoospermia due to single gene mutation", "Male infertility with teratozoospermia due to single gene mutation", "Male infertility with teratozoospermia due to single gene mutation (disorder)", "Male infertility with teratozoospermia due to single gene mutation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "male infertility with teratozoospermia due to single gene mutation", "shortest_name_length": 61}
{"curie": "MONDO:0032834", "names": ["RP86", "retinitis pigmentosa 86", "RETINITIS PIGMENTOSA 86"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 86", "shortest_name_length": 4}
{"curie": "MONDO:0006232", "names": ["GCT-ST", "Osteoclastoma of soft tissue", "Osteoclastoma of Soft Tissue", "Giant cell tumor of soft parts", "giant cell tumor of soft tissue", "Giant cell tumour of soft parts", "Giant Cell Tumor of Soft Tissue", "Giant cell tumor of soft tissue", "Giant cell tumour of soft tissue", "Giant cell tumor of soft parts NOS", "Giant cell tumour of soft parts NOS", "Giant cell tumor of soft parts, NOS", "Giant cell tumour of soft parts, NOS", "Giant Cell Tumor of Low Malignant Potential", "giant cell tumor of soft tissue (diagnosis)", "Giant cell tumor of soft parts (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "giant cell tumor of soft tissue", "shortest_name_length": 6}
{"curie": "MONDO:0005823", "names": ["Legionellosis", "Legionelloses", "legionellosis", "Legionellosis, NOS", "Legionnaires disease", "legionella infection", "Legionella infection", "LEGIONELLA INFECTIONS", "Legionella infections", "Legionella infection NOS", "Legionella infection, NOS", "Legionella infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "legionellosis", "shortest_name_length": 13}
{"curie": "MONDO:0008605", "names": ["TPT", "Nonopposable triphalangeal thumb", "TRIPHALANGEAL THUMB, NONOPPOSABLE", "Triphalangeal Thumb, Nonopposable", "triphalangeal thumb non opposable", "Triphalangeal thumb non opposable", "triphalangeal thumb, Nonopposable", "non-opposable triphalangeal thumb", "Non-opposable triphalangeal thumb"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "triphalangeal thumb, Nonopposable", "shortest_name_length": 3}
{"curie": "UMLS:C0348802", "names": ["rhinocerebral mucormycosis", "Rhinocerebral phycomycosis", "Rhinocerebral mucormycosis", "Rhinocerebral mucormycosis (disorder)", "rhinocerebral mucormycosis (diagnosis)", "RHINOCEREBRAL MUCORMYCOSIS PHYCOMYCOSIS", "RHINOCEREBRAL MUCORMYCOSIS <PHYCOMYCOSIS>"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rhinocerebral mucormycosis", "shortest_name_length": 26}
{"curie": "UMLS:C4745240", "names": ["Hormone Receptor-Positive Breast Carcinoma", "Hormone Receptor Positive Breast Carcinoma", "Hormone Receptor Positive Breast Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hormone Receptor-Positive Breast Carcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0007344", "names": ["CLUSTER HEADACHE, FAMILIAL", "cluster headache, familial", "Cluster Headache, Familial", "hereditary cluster headache syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cluster headache, familial", "shortest_name_length": 26}
{"curie": "MONDO:0006054", "names": ["Reproductive Tumor", "reproductive tumor", "reproductive neoplasm", "Reproductive Neoplasm", "Reproductive System Tumor", "reproductive system tumor", "Tumor of Reproductive System", "Reproductive System Neoplasm", "tumor of reproductive system", "reproductive system neoplasm", "neoplasm of reproductive system", "Neoplasm of Reproductive System", "Tumor of the Reproductive System", "tumor of the reproductive system", "neoplasm of the reproductive system", "Neoplasm of the Reproductive System", "reproductive system neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "reproductive system neoplasm", "shortest_name_length": 18}
{"curie": "MONDO:0019890", "names": ["Non-distal trisomy 9q", "non-distal trisomy 9q", "Non-telomeric trisomy 9q", "non-telomeric trisomy 9q", "Non-distal duplication 9q", "non-distal duplication 9q", "non-distal trisomy type 9q", "partial trisomy 9q non-distal", "Non-distal trisomy 9q (disorder)", "Non-distal trisomy 9q (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-distal trisomy 9q", "shortest_name_length": 21}
{"curie": "MONDO:0021450", "names": ["benign heart tumor", "Benign Heart Tumor", "benign Cardiac tumor", "Benign Cardiac Tumor", "benign heart neoplasm", "Benign Tumor of Heart", "Benign tumor of heart", "heart benign neoplasm", "Benign Heart Neoplasm", "benign tumor of heart", "Benign tumour of heart", "Benign cardiac neoplasm", "Benign Cardiac Neoplasm", "benign Cardiac neoplasm", "benign neoplasm of heart", "Benign neoplasm of heart", "Benign Neoplasm of Heart", "Benign Tumor of the Heart", "benign tumor of the heart", "Benign Neoplasm of the Heart", "unspecified cardiac neoplasm", "benign neoplasm of the heart", "Benign neoplasm of heart, NOS", "Benign neoplasm of heart (disorder)", "benign neoplasm of heart (diagnosis)", "unspecified benign neoplasm of heart", "unspecified benign neoplasm of heart (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of heart", "shortest_name_length": 18}
{"curie": "UMLS:C5447478", "names": ["Metastatic Malignant Thoracic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Malignant Thoracic Neoplasm", "shortest_name_length": 38}
{"curie": "MONDO:0004705", "names": ["Liver Fibroma", "liver fibroma", "hepatic fibroma", "Hepatic Fibroma", "fibroma of liver", "Fibroma of Liver", "Fibroma of the Liver", "fibroma of the liver", "benign fibroma of liver", "Liver Solitary Fibrous Tumor", "liver solitary fibrous tumor", "liver localized fibrous tumor", "Liver Localized Fibrous Tumor", "benign fibroma of liver (diagnosis)", "Liver Localized Fibrous Mesothelioma", "liver localized fibrous mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "liver solitary fibrous tumor", "shortest_name_length": 13}
{"curie": "UMLS:C0519066", "names": ["Acute Q Fever", "Q FEVER ACUTE", "Acute Q fever", "Fever, Acute Q", "Q Fever, Acute", "Acute Q Fevers", "Fevers, Acute Q", "Q Fevers, Acute", "Acute Q fever (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Q fever", "shortest_name_length": 13}
{"curie": "MONDO:0030323", "names": ["SCAR31", "autosomal recessive spinocerebellar ataxia 31", "spinocerebellar ataxia, autosomal recessive 31", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 31"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia, autosomal recessive 31", "shortest_name_length": 6}
{"curie": "MONDO:0012712", "names": ["DYTCA", "Dystonia with Cerebellar Atrophy", "dystonia with cerebellar atrophy", "DYSTONIA WITH CEREBELLAR ATROPHY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dystonia with cerebellar atrophy", "shortest_name_length": 5}
{"curie": "UMLS:C0038565", "names": ["SUBPHRENIC ABSCESS", "Subphrenic Abscess", "subphrenic abscess", "Abscess;subphrenic", "Subphrenic abscess", "Abscess, Subphrenic", "subphrenic; abscess", "ABSCESS, SUBPHRENIC", "abscess; subphrenic", "Subphrenic Abscesses", "Abscesses, Subphrenic", "subdiaphragmatic abscess", "Subdiaphragmatic abscess", "Subdiaphragmatic Abscess", "ABSCESS, SUBDIAPHRAGMATIC", "Abscess, Subdiaphragmatic", "Subdiaphragmatic Abscesses", "Abscesses, Subdiaphragmatic", "subphrenic abscess (diagnosis)", "Subdiaphragmatic abscess (disorder)", "subdiaphragmatic abscess (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subphrenic Abscess", "shortest_name_length": 18}
{"curie": "MONDO:0011413", "names": ["CATC1", "CTRCT9", "CRYAA cataract (disease)", "cataract 9 multiple types", "cataract 9, multiple types", "Cataract 9, Multiple Types", "CATARACT 9, MULTIPLE TYPES", "cataract, autosomal dominant", "CATARACT, AUTOSOMAL DOMINANT", "Cataract, Autosomal Dominant", "autosomal recessive congenital cataract 1", "CATARACT, AUTOSOMAL RECESSIVE CONGENITAL 1", "Cataract, Autosomal Recessive Congenital 1", "cataract, autosomal recessive congenital 1", "cataract (disease) caused by mutation in CRYAA", "cataract 9 multiple types with or without microcornea", "CATARACT 9, MULTIPLE TYPES, WITH OR WITHOUT MICROCORNEA", "cataract 9, multiple types, with or without microcornea", "Cataract 9, multiple types, with or without microcornea"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 9 multiple types", "shortest_name_length": 5}
{"curie": "UMLS:C1306341", "names": ["mental handicap", "Mental handicap", "handicap mental", "handicaps mental", "mental; handicap", "handicap; mental", "Mental disability", "mental disability", "Mental impairment", "handicapped mental", "Mental subnormality", "Mental handicap NOS", "disabilities mental", "mental; handicapped", "mental subnormality", "handicapped; mental", "MH - Mental handicap", "Mental impairment NOS", "Mental disability NOS", "Mental subnormality NOS", "mental disability (history)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mental handicap", "shortest_name_length": 15}
{"curie": "MONDO:0004292", "names": ["supraglottic verrucous carcinoma", "supraglottis verrucous carcinoma", "Supraglottis Verrucous Carcinoma", "Supraglottic Verrucous Carcinoma", "Verrucous Carcinoma of Supraglottis", "verrucous carcinoma of Supraglottis", "verrucous carcinoma of supraglottis", "verrucous carcinoma of the supraglottis", "Verrucous Carcinoma of the Supraglottis", "supraglottic part of larynx verrucous carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "supraglottis verrucous carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0021514", "names": ["benign pericardial tumor", "Benign Pericardial Tumor", "pericardium benign neoplasm", "Benign Pericardial Neoplasm", "Benign Tumor of Pericardium", "Benign pericardium neoplasm", "benign tumor of pericardium", "benign pericardial neoplasm", "Benign neoplasm of pericardium", "Benign Neoplasm of Pericardium", "benign neoplasm of pericardium", "benign tumor of the pericardium", "Benign Tumor of the Pericardium", "benign neoplasm of the pericardium", "Benign Neoplasm of the Pericardium", "Benign neoplasm of pericardium (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of pericardium", "shortest_name_length": 24}
{"curie": "MONDO:0015365", "names": ["autosomal dominant hereditary sensory and autonomic neuropathy", "hereditary sensory and autonomic neuropathy, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant hereditary sensory and autonomic neuropathy", "shortest_name_length": 62}
{"curie": "MONDO:0014711", "names": ["CMT2W", "Charcot-Marie-Tooth neuropathy type 2W", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2W", "Charcot-Marie-Tooth neuropathy, type 2W", "HARS Charcot-Marie-Tooth disease type 2", "Charcot-Marie-Tooth disease, axonal type 2W", "Charcot-Marie-Tooth disease, axonal, type 2W", "Charcot-Marie-Tooth disease, axonal, type 2w", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2W", "autosomal dominant Charcot-Marie-Tooth disease type 2W", "Autosomal dominant Charcot-Marie-Tooth disease type 2W", "Charcot-Marie-Tooth disease type 2 caused by mutation in HARS", "autosomal dominant axonal Charcot-Marie-Tooth disease type 2W", "Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2W", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2W", "Autosomal dominant Charcot-Marie-Tooth disease type 2W (disorder)", "Autosomal dominant Charcot-Marie-Tooth disease type 2 due to HARS mutation", "autosomal dominant Charcot-Marie-Tooth disease type 2 due to HARS mutation", "Autosomal dominant Charcot-Marie-Tooth disease type 2 due to HARS (histidyl-tRNA synthetase 1) mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant Charcot-Marie-Tooth disease type 2W", "shortest_name_length": 5}
{"curie": "UMLS:C0280151", "names": ["Stage II Immunoblastic Lymphoma", "Stage II Adult Immunoblastic Lymphoma", "Ann Arbor Stage II Adult Immunoblastic Lymphoma", "Stage II Adult Immunoblastic Large Cell Lymphoma", "stage II adult immunoblastic large cell lymphoma", "Adult Immunoblastic Large Cell Lymphoma Stage II", "adult immunoblastic large cell lymphoma, stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Adult Immunoblastic Lymphoma", "shortest_name_length": 31}
{"curie": "MONDO:0003396", "names": ["Epulis", "epulis", "epulides", "Epulides", "Gum Polyp", "gum polyp", "Epulis, NOS", "polyp of gum", "Polyp of Gum", "polyp of Gum", "gingiva polyp", "polyp; gingiva", "gingiva; polyp", "gingival polyp", "Gingival polyp", "Gingival Polyp", "polyp of the gum", "Epulis (finding)", "polyp of gingiva", "Polyp of Gingiva", "Polyp of the Gum", "Polyp of the Gingiva", "polyp of the gingiva", "Gingival polyp (disorder)", "Localized gingival enlargement", "Localised gingival enlargement", "Epulis (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epulis", "shortest_name_length": 6}
{"curie": "MONDO:0005602", "names": ["ovary teratoma", "teratoma ovary", "OVARY, TERATOMA", "ovary; teratoma", "teratoma; ovary", "ovary teratomas", "Ovarian teratoma", "Ovarian Teratoma", "OVARIAN TERATOMA", "teratoma ovarian", "ovarian teratoma", "teratoma of ovary", "teratoma, ovarian", "Teratoma of Ovary", "ovaries teratomas", "Teratoma of ovary", "TERATOMA, OVARIAN", "ovarian teratomas", "teratoma of the ovary", "Teratoma of the Ovary", "teratoma ovarian cancer", "OVARIAN CANCER, TERATOMA", "Ovarian Germ Cell Teratoma", "ovarian germ cell teratoma", "Ovarian germ cell teratoma", "germ cell teratoma of ovary", "Germ Cell Teratoma of Ovary", "germ cell teratoma of Ovary", "Teratoma of ovary (disorder)", "teratoma of ovary (diagnosis)", "germ cell teratoma of the ovary", "Germ Cell Teratoma of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian teratoma", "shortest_name_length": 14}
{"curie": "MONDO:0060582", "names": ["ANOA", "auditory neuropathy and optic atrophy", "AUDITORY NEUROPATHY AND OPTIC ATROPHY", "Auditory neuropathy-optic atrophy syndrome", "auditory neuropathy-optic atrophy syndrome", "Auditory neuropathy, optic atrophy syndrome", "Auditory neuropathy, optic atrophy syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "auditory neuropathy-optic atrophy syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0014023", "names": ["CDGIu", "CDG1U", "CDG-Iu", "CDG Iu", "DPM2-CDG", "CDG syndrome type Iu", "congenital disorder of glycosylation 1u", "congenital disorder of glycosylation Iu", "Congenital disorder of glycosylation type Iu", "Congenital disorder of glycosylation type 1u", "congenital disorder of glycosylation type 1u", "congenital disorder of glycosylation type Iu", "congenital disorder of glycosylation, type Iu", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu", "CMD with intellectual disability and severe epilepsy", "Carbohydrate deficient glycoprotein syndrome type Iu", "Carbohydrate deficient glycoprotein syndrome type 1u", "carbohydrate deficient glycoprotein syndrome type Iu", "Congenital muscular dystrophy with intellectual disability and severe epilepsy", "congenital muscular dystrophy with intellectual disability and severe epilepsy", "Congenital muscular dystrophy with intellectual disability and severe epilepsy (disorder)", "congenital muscular dystrophy with intellectual disability and severe epilepsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital muscular dystrophy with intellectual disability and severe epilepsy", "shortest_name_length": 5}
{"curie": "MONDO:0045054", "names": ["Oncologic Complications", "oncologic complications", "cancer-related condition", "Cancer-Related Condition", "Cancer Related Condition", "cancer-related problem/condition", "cancer related problem/condition", "problem/condition, cancer related", "problem/condition, cancer-related", "cancer-related problem or condition", "Cancer-Related Problem or Condition", "Cancer- and cancer treatment-related conditions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cancer-related condition", "shortest_name_length": 23}
{"curie": "MONDO:0011797", "names": ["Iahsp", "IAHSP", "spastic paralysis, infantile onset ascending", "Spastic Paralysis, Infantile Onset Ascending", "Spastic Paralysis, Infantile-Onset Ascending", "SPASTIC PARALYSIS, INFANTILE-ONSET ASCENDING", "spastic paralysis, infantile-onset ascending", "Infantile ascending hereditary spastic paralysis", "Infantile-onset ascending hereditary spastic paralysis", "Infantile-Onset Ascending Hereditary Spastic Paralysis", "infantile-onset ascending hereditary spastic paralysis", "Hereditary spastic paralysis, infantile onset ascending", "Infantile ascending hereditary spastic paralysis (disorder)", "IAHSP - infantile onset ascending hereditary spastic paralysis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile-onset ascending hereditary spastic paralysis", "shortest_name_length": 5}
{"curie": "MONDO:0012959", "names": ["PSORS11", "psoriasis 11", "psoriasis susceptibility 11", "PSORIASIS 11, SUSCEPTIBILITY TO", "psoriasis 11, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "psoriasis 11, susceptibility to", "shortest_name_length": 7}
{"curie": "MONDO:0007388", "names": ["Congenital short costocoracoid ligament", "Congenitally short costocoracoid ligament", "costocoracoid ligament congenitally short", "Costocoracoid ligament congenitally short", "congenitally short costocoracoid ligament", "Costocoracoid Ligament, Congenitally Short", "COSTOCORACOID LIGAMENT, CONGENITALLY SHORT", "costocoracoid ligament, congenitally short", "congenital shortness of the costocoracoid ligament", "Congenital short costocoracoid ligament (disorder)", "Congenital shortness of the costocoracoid ligament", "fixation of the scapula to the first rib by a congenitally short costocoracoid ligament"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenitally short costocoracoid ligament", "shortest_name_length": 39}
{"curie": "MONDO:0008688", "names": ["WTsyndrome", "WT syndrome", "WT Limb-Blood Syndrome", "WT limb-blood syndrome", "WT LIMB-BLOOD SYNDROME", "WT limb blood syndrome", "WT limb blood syndrome (disorder)", "Radial-ulnar hypoplasia with bone marrow failure and-or leukemia", "radial-ulnar hypoplasia with bone marrow failure and/or leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "WT limb-blood syndrome", "shortest_name_length": 10}
{"curie": "UMLS:C0235453", "names": ["STEROID WITHDRAWAL SYNDROME", "Steroid withdrawal syndrome", "Withdrawal syndrome corticosteroid", "WITHDRAWAL SYNDROME CORTICOSTEROID", "Syndrome corticosteroid withdrawal", "Corticosteroid withdrawal syndrome", "SYNDROME CORTICOSTEROID WITHDRAWAL", "CORTICOSTEROID WITHDRAWAL SYNDROME", "Steroid withdrawal syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Steroid withdrawal syndrome", "shortest_name_length": 27}
{"curie": "UMLS:C5446655", "names": ["Breast PmA", "Breast Polymorphous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Polymorphous Adenocarcinoma", "shortest_name_length": 10}
{"curie": "MONDO:0024376", "names": ["disorders of initiating and maintaining sleep", "sleep disorder, initiating and maintaining sleep"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sleep disorder, initiating and maintaining sleep", "shortest_name_length": 45}
{"curie": "MONDO:0010598", "names": ["XLG1", "PYKL", "XLG2", "GSD9A", "GSD9A1", "GSD9A2", "GSD VIII", "GSD IXA2", "GSD IXa2", "GSD type 9A", "GSD type IXa", "GSD type IXA1", "Glycogenosis 8", "GSD8, FORMERLY", "GSD VIII, FORMERLY", "GSD VIII, formerly", "glycogenosis type 8", "Hepatic glycogenosis", "glycogenosis type 9A", "glycogenosis type IXa", "glycogenosis type VIII", "Glycogenosis type VIII", "Glycogen storage disease 8", "glycogen storage disease 8", "glycogen storage disease IXa", "glycogen storage disease IXa1", "glycogen storage disease VIII", "GLYCOGEN STORAGE DISEASE IXa1", "GLYCOGEN STORAGE DISEASE IXa2", "PHKA2 glycogen storage disease", "Glycogen storage disease type 8", "glycogen storage disease type 9A", "glycogen storage disease type IXa", "glycogen storage disease type IXA1", "Glycogen storage disease type VIII", "Glycogen Storage Disease Type VIII", "glycogen storage disease type VIII", "GLYCOGEN STORAGE DISEASE, TYPE IXa1", "GLYCOGEN STORAGE DISEASE, TYPE IXa2", "Glycogen Storage Disease, Type IXA2", "Glycogen storage disease, type VIII", "LIVER GLYCOGENOSIS, X-LINKED, TYPE I", "liver glycogenosis, X-linked, type 1", "LIVER GLYCOGENOSIS, X-LINKED, TYPE II", "Liver Glycogenosis, X-Linked, Type II", "hepatic phosphorylase kinase deficiency", "glycogen storage disease VIII, formerly", "GLYCOGEN STORAGE DISEASE VIII, FORMERLY", "phosphorylase kinase deficiency of liver", "Glycogenosis due to inactive phosphorylase", "Glycogen storage disease type VIII (disorder)", "glycogen storage disease type IXA1 (diagnosis)", "PHKA2-related glycogen storage disease type IX", "hepatic glycogen phosphorylase kinase deficiency", "Hepatic glycogen phosphorylase kinase deficiency", "glycogen storage disease caused by mutation in PHKA2", "glycogen storage disease, type IXa1, X-linked recessive", "glycogen storage disease, type IXa2, X-linked recessive", "Hepatic glycogen phosphorylase kinase deficiency (disorder)", "Glycogenosis due to inactive hepatic glycogen phosphorylase"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease IXa1", "shortest_name_length": 4}
{"curie": "UMLS:C4331347", "names": ["Stage IVC Lip and Oral Cavity Cancer", "Stage IVC Lip and Oral Cavity Cancer AJCC v8", "Stage IVC Lip and Oral Cavity Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Lip and Oral Cavity Cancer AJCC v8", "shortest_name_length": 36}
{"curie": "MONDO:0020071", "names": ["infantile epilepsy syndrome", "epilepsy syndrome of infancy", "infantile onset epilepsy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile epilepsy syndrome", "shortest_name_length": 27}
{"curie": "MONDO:0032485", "names": ["MRD61", "INTELLECTUAL DEVELOPMENTAL DISORDER 61", "intellectual developmental disorder 61", "Mental Retardation, Autosomal Dominant 61", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 61", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 61"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder 61", "shortest_name_length": 5}
{"curie": "MONDO:0023243", "names": ["craniosynostosis brachydactyly", "glass-chapman-hockley syndrome", "glass chapman hockley syndrome", "craniosynostosis - dysmorphism - brachydactyly", "craniosynostosis-dysmorphism-brachydactyly syndrome", "craniosynostosis with facial dysmorphism and brachydactyly syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glass-chapman-hockley syndrome", "shortest_name_length": 30}
{"curie": "MONDO:0000812", "names": ["Spondylopathy", "SPINE DISEASE", "SPONDYLOPATHY", "spine disease", "spondylopathy", "Spinal Disease", "spine disorder", "spinal disease", "spinal diseases", "spinal disorder", "Spinal disorder", "Disease, Spinal", "Spinal Diseases", "spondylopathies", "Spine--Diseases", "Spondylopathies", "disease of spine", "Diseases, Spinal", "Disorder of spine", "disorder of spine", "Spondylopathy, NOS", "Spinal disorder NOS", "Spinal disorder, NOS", "Vertebral arthropathy", "vertebral column disease", "vertebral column disorder", "Unspecified spondylopathy", "Vertebral column disorder", "spondylopathy (diagnosis)", "Disorder of spinal column", "Spondylopathies (M45-M49)", "Spondylopathy, unspecified", "Vertebral arthropathy, NOS", "disease of vertebral column", "disorder of vertebral column", "Disorder of vertebral column", "DISORDERS OF THE VERTEBRAL COLUMN", "vertebral column disease or disorder", "Disorder of the vertebral column, NOS", "disease or disorder of vertebral column", "Disorder of vertebral column (disorder)", "disorder of vertebral column (diagnosis)", "disease (or disorder); vertebra, spondylopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vertebral column disorder", "shortest_name_length": 13}
{"curie": "UMLS:C4553883", "names": ["Stage IVA Thyroid Gland Medullary Cancer", "Stage IVA Thyroid Gland Medullary Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Thyroid Gland Medullary Carcinoma AJCC v8", "shortest_name_length": 40}
{"curie": "MONDO:0002291", "names": ["granular cell skin tumor", "skin granular cell tumor", "Granular Cell Skin Tumor", "skin granular cell tumour", "Skin Granular Cell Neoplasm", "Granular cell tumor of skin", "skin granular cell neoplasm", "Granular Cell Tumor of Skin", "granular cell tumor of skin", "Abrikossoff's tumor of skin", "Abrikossoff's tumour of skin", "granular cell tumour of skin", "Granular cell tumour of skin", "cutaneous granular cell tumor", "Cutaneous Granular Cell Tumor", "Granular Cell Neoplasm of Skin", "granular cell neoplasm of skin", "Granular Cell Tumor of the Skin", "granular cell tumor of the skin", "zone of skin granular cell tumor", "Cutaneous Granular Cell Neoplasm", "cutaneous granular cell neoplasm", "Granular cell myoblastoma of skin", "granular cell neoplasm of the skin", "Granular Cell Neoplasm of the Skin", "granular cell tumor of zone of skin", "Granular cell tumor of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous granular cell tumor", "shortest_name_length": 24}
{"curie": "MONDO:0001674", "names": ["diverticulitis colon", "colon diverticulitis", "Colon diverticulitis", "Colonic Diverticulitis", "diverticulitis colonic", "Colonic diverticulitis", "colonic diverticulitis", "Diverticulitis of Colon", "Diverticulitis of colon", "diverticulitis of colon", "Diverticulitis, Colonic", "COLON NOS DIVERTICULITIS", "colonic diverticular disease", "Diverticulitis of colon (disorder)", "diverticulitis of colon (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diverticulitis of colon", "shortest_name_length": 20}
{"curie": "MONDO:0015225", "names": ["arthrogryposis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0018973", "names": ["Pattern dystrophy", "MACULAR DYSTROPHY, BUTTERFLY-SHAPED PIGMENTARY", "Macular dystrophy, butterfly-shaped pigmentary", "Butterfly-shaped pigment dystrophy of the fovea", "BUTTERFLY DYSTROPHY OF RETINAL PIGMENT EPITHELIUM", "Butterfly dystrophy of retinal pigment epithelium", "PATTERNED DYSTROPHY OF RETINAL PIGMENT EPITHELIUM", "Patterned dystrophy of retinal pigment epithelium", "patterned dystrophy of the retinal pigment epithelium", "Patterned dystrophy of the retinal pigment epithelium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "patterned dystrophy of the retinal pigment epithelium", "shortest_name_length": 17}
{"curie": "MONDO:0019745", "names": ["cystinuria type A", "Cystinuria type A", "CYSTINURIA, TYPE A", "Cystinuria, Type A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cystinuria type A", "shortest_name_length": 17}
{"curie": "UMLS:C1168250", "names": ["Laryngopharyngeal reflux", "laryngopharyngeal reflux", "Laryngopharyngeal Reflux", "Reflux, Laryngopharyngeal", "Laryngopharyngeal reflux (disorder)", "laryngopharyngeal reflux (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laryngopharyngeal Reflux", "shortest_name_length": 24}
{"curie": "UMLS:C0162286", "names": ["Esophagus burn", "ESOPHAGUS BURN", "Burn esophageal", "Oesophagus burn", "Esophageal burn", "burn; esophagus", "ESOPHAGEAL BURN", "esophagus; burn", "burns esophagus", "burns esophageal", "burned esophagus", "Burn oesophageal", "OESOPHAGEAL BURN", "Oesophageal burn", "burns oesophagus", "Burning esophagus", "esophagus burning", "Burn of esophagus", "burning esophagus", "Burn of Esophagus", "burns of esophagus", "Burn of oesophagus", "Burning oesophagus", "burns esophagus thermal", "ESOPHAGEAL BURN THERMAL", "Burning (in);oesophagus", "Thermal burn esophageal", "Thermal burn oesophageal", "Thermal burn of esophagus", "Thermal burn of oesophagus", "Burn of esophagus (disorder)", "burns of esophagus (diagnosis)", "burning sensation in the esophagus", "burning sensation in the oesophagus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Burn of esophagus", "shortest_name_length": 14}
{"curie": "UMLS:C3897520", "names": ["Stage IVA Rectal Cancer", "Stage IVA Rectal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Rectal Cancer AJCC v7", "shortest_name_length": 23}
{"curie": "MONDO:0021052", "names": ["Parasympathetic paraganglioma", "Parasympathetic Paraganglioma", "parasympathetic paraganglioma", "parasympathetic Paraganglionic neoplasm", "Parasympathetic Paraganglionic Neoplasm", "parasympathetic Extra-adrenal paraganglioma", "Parasympathetic Extra-Adrenal Paraganglioma", "parasympathetic nervous system paraganglioma", "paraganglioma of parasympathetic nervous system", "Parasympathetic paraganglioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parasympathetic paraganglioma", "shortest_name_length": 29}
{"curie": "MONDO:0020720", "names": ["xlh", "XLH", "HVDRR", "VDDR II", "VDRR II", "hypophosphatemic ricket", "hypophosphatemic rickets", "hypophosphatemia rickets", "X Linked Hypophosphatemia", "X-linked hypophosphatemia", "hypophosphataemic rickets", "X-Linked Hypophosphatemia", "familial hypophosphatemia", "Hypophosphatemia, X-Linked", "X-linked hypophosphataemia", "Calcitriol receptor defect", "Hypophosphatemia, X Linked", "vitamin D resistant rickets", "vitamin d-resistant rickets", "vitamin d resistant rickets", "Vitamin D Dependent Rickets 2b", "Rickets familial hypophosphatemic", "hypophosphatemic rickets x linked", "X-linked Hypophosphatemic Rickets", "X-linked hypophosphatemic rickets", "X-Linked Hypophosphatemic Rickets", "Familial Hypophosphatemic Rickets", "Familial hypophosphatemic rickets", "Rickets, Familial Hypophosphatemic", "Rickets, X-Linked Hypophosphatemic", "Rickets familial hypophosphataemic", "Familial hypophosphataemic rickets", "Hypophosphatemic Rickets, Familial", "Type 2 vitamin D-dependent rickets", "Hypophosphatemic Rickets, X-Linked", "Vitamin D-resistant rickets type II", "Vitamin D-dependent rickets, type 2", "Vitamin D-dependent rickets type II", "Hereditary Hypophosphatemic Rickets", "Hereditary hypophosphatemic rickets", "type II vitamin D dependent rickets", "familial hypophosphatemia in rickets", "Rickets, Hereditary Hypophosphatemic", "X linked hypophosphatemia in rickets", "Hereditary hypophosphataemic rickets", "Familial vitamin D-resistant rickets", "Hypophosphatemic Rickets, Hereditary", "Familial hypophosphatemic bone disease", "Hereditary vitamin D-resistant rickets", "Hereditary Vitamin D-Resistant Rickets", "Hereditary Vitamin D Resistant Rickets", "Familial hypophosphataemic bone disease", "Rickets, Hereditary Vitamin D Resistant", "Vitamin D Resistant Rickets, Hereditary", "RICKETS, HEREDITARY VITAMIN D-RESISTANT", "Vitamin D-Resistant Rickets, Hereditary", "Rickets, Hereditary Vitamin D-Resistant", "HYPOCALCEMIC VITAMIN D-RESISTANT RICKETS", "Hypocalcemic vitamin D-resistant rickets", "Hypocalcemic Vitamin D Resistant Rickets", "Hypocalcemic Vitamin D-Resistant Rickets", "Vitamin D-dependent rickets, type 2 (disorder)", "type II vitamin D dependent rickets (diagnosis)", "GENERALIZED RESISTANCE TO 1,25-DIHYDROXYVITAMIN D", "Generalized Resistance To 1,25 Dihydroxyvitamin D", "Generalized Resistance To 1,25-Dihydroxyvitamin D", "X-linked hypophosphatemic rickets (recessive or dominant)", "End organ unresponsiveness to 1,25-dihydroxycholecalciferol", "Vitamin D-Resistant Rickets With End-Organ Unresponsiveness To 1,25-Dihydroxycholecalciferol", "VITAMIN D-RESISTANT RICKETS WITH END-ORGAN UNRESPONSIVENESS TO 1,25-DIHYDROXYCHOLECALCIFEROL", "Vitamin D Resistant Rickets With End Organ Unresponsiveness To 1,25 Dihydroxycholecalciferol", "Hereditary 1,25 Dihydroxyvitamin D-Resistant Rickets with Abnormal Vitamin D Receptor without Alopecia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked hypophosphatemic rickets", "shortest_name_length": 3}
{"curie": "MONDO:0023193", "names": ["Friedman Goodman syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Friedman Goodman syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0025371", "names": ["Parvovirus", "parvovirus", "Parvovirus NOS", "Parvovirus infection", "Parvovirus infections", "infection, Parvovirus", "infections, Parvovirus", "Parvoviridae infection", "Parvoviridae Infection", "Parvoviridae Infections", "infection, Parvoviridae", "Infection, Parvoviridae", "infections, Parvoviridae", "Infections, Parvoviridae", "disease due to parvoviridae", "disease due to Parvoviridae", "Disease due to Parvoviridae", "DISEASES DUE TO PARVOVIRIDAE", "disease caused by Parvoviridae", "Disease caused by Parvoviridae", "Parvoviridae infectious disease", "Parvoviridae disease or disorder", "Disease due to Parvoviridae, NOS", "Parvoviridae caused disease or disorder", "Disease caused by Parvoviridae (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parvoviridae infectious disease", "shortest_name_length": 10}
{"curie": "MONDO:0020288", "names": ["atrioventricular valve anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrioventricular valve anomaly", "shortest_name_length": 30}
{"curie": "MONDO:0008935", "names": ["CAHH", "GDHS", "Gordon-Holmes syndrome", "Gordon Holmes syndrome", "Gordon Holmes Syndrome", "GORDON HOLMES SYNDROME", "LHRH Deficiency and Ataxia", "LHRH deficiency and ataxia", "LHRH DEFICIENCY AND ATAXIA", "cerebellar ataxia - hypogonadism", "cerebellar ataxia-hypogonadism syndrome", "Cerebellar ataxia-hypogonadism syndrome", "Progressive cerebellar ataxia with hypogonadism", "cerebellar ataxia and hypogonadotropic hypogonadism", "CEREBELLAR ATAXIA AND HYPOGONADOTROPIC HYPOGONADISM", "Cerebellar Ataxia and Hypogonadotropic Hypogonadism", "Progressive cerebellar ataxia with hypogonadism (disorder)", "Luteinizing hormone-releasing hormone deficiency with ataxia", "luteinizing hormone-releasing hormone deficiency with ataxia", "Luteinising hormone-releasing hormone deficiency with ataxia", "luteinizing hormone releasing hormone, deficiency of with ataxia", "LUTEINIZING HORMONE-RELEASING HORMONE, DEFICIENCY OF, WITH ATAXIA", "Luteinizing Hormone-Releasing Hormone, Deficiency of, with Ataxia", "luteinizing hormone-releasing hormone, deficiency of, with ataxia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellar ataxia-hypogonadism syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C5419971", "names": ["Digestive System Solitary Fibrous Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Digestive System Solitary Fibrous Tumor", "shortest_name_length": 39}
{"curie": "UMLS:C1334670", "names": ["Mediastinal Teratocarcinoma", "Teratocarcinoma of Mediastinum", "teratocarcinoma of mediastinum", "Teratocarcinoma of the Mediastinum", "teratocarcinoma of mediastinum (diagnosis)", "Mediastinal Mixed Embryonal Carcinoma and Teratoma", "Mixed Embryonal Carcinoma and Teratoma of Mediastinum", "Mixed Embryonal Carcinoma and Teratoma of the Mediastinum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "teratocarcinoma of mediastinum", "shortest_name_length": 27}
{"curie": "UMLS:C0751020", "names": ["Vertebrobasilar Circulation Transient Ischemic Attack", "Transient Ischemic Attack, Vertebrobasilar Circulation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transient Ischemic Attack, Vertebrobasilar Circulation", "shortest_name_length": 53}
{"curie": "MONDO:0006632", "names": ["osteoarthritis, hand"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteoarthritis, hand", "shortest_name_length": 20}
{"curie": "MONDO:0004840", "names": ["Acquired renal cyst", "kidney cyst acquired", "cyst; renal, acquired", "cyst; kidney, acquired", "acquired cyst of kidney", "Cyst of kidney, acquired", "non-congenital cyst of kidney", "acquired renal cystic disease", "Acquired renal cystic disease", "Cyst of kidney, not congenital", "ACQUIRED RENAL CYSTIC DISEASES", "acquired cyst of kidney (diagnosis)", "Acquired renal cystic disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-congenital cyst of kidney", "shortest_name_length": 19}
{"curie": "UMLS:C0549483", "names": ["ABSCESS BACTERIAL", "Abscess bacterial", "Abscess bacterial NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abscess bacterial", "shortest_name_length": 17}
{"curie": "UMLS:C0862970", "names": ["Resectable Bile Duct Adenocarcinoma", "Bile duct adenocarcinoma resectable"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bile duct adenocarcinoma resectable", "shortest_name_length": 35}
{"curie": "MONDO:0800176", "names": ["Latrodectism", "latrodectism", "LACTRODECTISM", "black widow envenomation", "black-widow-spider; syndrome", "syndrome; black-widow-spider", "black widow spider envenomation", "poisoning due to black widow spider", "Poisoning by black widow spider bite", "toxic effect of venom of black widow", "poisoning caused by black widow venom", "Poisoning by Lactrodectus mactans bite", "Poisoning due to black widow spider venom", "Poisoning caused by black widow spider venom", "Poisoning caused by black widow spider venom (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "black widow spider envenomation", "shortest_name_length": 12}
{"curie": "UMLS:C4528408", "names": ["Advanced Head and Neck Squamous Cell Cancer", "Advanced Head and Neck Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Head and Neck Squamous Cell Carcinoma", "shortest_name_length": 43}
{"curie": "UMLS:C1336154", "names": ["Stage IIA Bladder Cancer", "Stage IIA Urinary Bladder Cancer", "Stage IIA Urinary Bladder Carcinoma", "Jewett-Marshall Stage B1 Bladder Cancer", "Jewett-Marshall Stage B1 Urinary Bladder Cancer", "Jewett-Marshall Stage B1 Urinary Bladder Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Bladder Cancer", "shortest_name_length": 24}
{"curie": "UMLS:C1335368", "names": ["Passive-Aggressive Behavior"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Passive-Aggressive Behavior", "shortest_name_length": 27}
{"curie": "UMLS:C4683471", "names": ["Thyroid Gland Medullary Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Medullary Carcinoma by AJCC v7 Stage", "shortest_name_length": 50}
{"curie": "UMLS:C0333865", "names": ["Atypical", "atypical cell", "Atypical cell", "atypical cells", "atypicals cells", "cellular atypia", "Cytologic atypia", "cytologic atypia", "Cytologic Atypia", "Atypia, cellular", "Atypia, cytologic", "Cytologic Atypias", "CYTOLOGIC ATYPIAS", "Atypical Cell Present", "Cytologic atypia, NOS", "Atypical cell present", "Atypical cell present, NOS", "Cytologic atypia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cytologic atypia", "shortest_name_length": 8}
{"curie": "UMLS:C4087393", "names": ["Marginal zone lymphoma refractory", "Refractory Marginal Zone Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Marginal zone lymphoma refractory", "shortest_name_length": 33}
{"curie": "MONDO:0019165", "names": ["CPP", "True Precocious Puberty", "Central precocious puberty", "Central Precocious Puberty", "central precocious puberty", "Puberty, Central Precocious", "precocious puberty, central", "Precocious Puberty, Central", "puberty; precocious, central", "precocious; puberty, central", "Central Precocious Puberties", "Precocious Puberties, Central", "Puberties, Central Precocious", "Central precocious puberty (disorder)", "[OBSOLETE] Precocious Puberty, Central", "central precocious puberty (diagnosis)", "Gonadotropin dependent precocious puberty", "Gonadotropin-Dependent Precocious Puberty", "Gonadotropin-dependant precocious puberty", "Gonadotropin-dependent precocious puberty", "gonadotropin-dependant precocious puberty", "gonadotropin-dependent precocious puberty", "Gonadotropin-releasing Hormone-dependent Precocious Puberty"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central precocious puberty", "shortest_name_length": 3}
{"curie": "MONDO:0009487", "names": ["Keratoconus And Congenital Hip Dysplasia", "KERATOCONUS AND CONGENITAL HIP DYSPLASIA", "keratoconus and congenital hip dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratoconus and congenital hip dysplasia", "shortest_name_length": 40}
{"curie": "MONDO:0006134", "names": ["Adenosquamous Carcinoma", "CERVICAL CANCER ADENOSQUAMOUS", "cervical adenosquamous cancer", "Cervical Adenosquamous Cancer", "cervical adenosquamous carcinoma", "Cervical adenosquamous carcinoma", "Cervical Adenosquamous Carcinoma", "adenosquamous carcinoma of cervix", "Adenosquamous carcinoma of cervix", "Cervix Adenosquamous Cell Carcinoma", "cervix adenosquamous cell carcinoma", "Adenosquamous carcinoma of the cervix", "Cervical Adenosquamous Cell Carcinoma", "cervical adenosquamous cell carcinoma", "adenosquamous cell carcinoma of cervix", "Adenosquamous Cell Carcinoma of Cervix", "adenosquamous cell cancer of the cervix", "cancer of the cervix, adenosquamous cell", "cervix uteri adenosquamous cell carcinoma", "Cervix Uteri Adenosquamous Cell Carcinoma", "Adenosquamous Cell Carcinoma of the Cervix", "adenosquamous cell carcinoma of the cervix", "Uterine Cervix Adenosquamous Cell Carcinoma", "uterine cervix adenosquamous cell carcinoma", "cervix cancer, adenosquamous cell carcinoma", "carcinoma of the cervix, adenosquamous cell", "Adenosquamous Cell Carcinoma of Cervix Uteri", "Adenosquamous carcinoma of cervix (disorder)", "adenosquamous cell carcinoma of cervix uteri", "cervical cancer, adenosquamous cell carcinoma", "adenosquamous carcinoma of cervix (diagnosis)", "Adenosquamous Cell Carcinoma of Uterine Cervix", "adenosquamous cell carcinoma of uterine cervix", "Adenosquamous Cell Carcinoma of the Cervix Uteri", "adenosquamous cell carcinoma of the cervix uteri", "Adenosquamous cell carcinoma of the Cervix Uteri", "Adenosquamous Cell Carcinoma of the Uterine Cervix", "adenosquamous cell carcinoma of the uterine cervix", "uterine cervix cancer, adenosquamous cell carcinoma", "uterine cervical cancer, adenosquamous cell carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical adenosquamous carcinoma", "shortest_name_length": 23}
{"curie": "MONDO:0023030", "names": ["dysmorphism cleft palate loose skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dysmorphism cleft palate loose skin", "shortest_name_length": 35}
{"curie": "UMLS:C0729554", "names": ["Mediastinal infection", "infection; mediastinum", "mediastinum; infection", "infectious mediastinitis", "Infectious mediastinitis", "Infectious Mediastinitis", "Infectious mediastinitis (disorder)", "infectious mediastinitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infectious Mediastinitis", "shortest_name_length": 21}
{"curie": "UMLS:C2981396", "names": ["Stage III Appendix Carcinoid Tumor", "Stage III Appendix Neuroendocrine Tumor", "Stage III Appendix Carcinoid Tumor AJCC v7", "Stage III Appendix Neuroendocrine Tumor AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Appendix Neuroendocrine Tumor AJCC v7", "shortest_name_length": 34}
{"curie": "UMLS:C5420061", "names": ["Sinonasal Neurofibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Neurofibroma", "shortest_name_length": 22}
{"curie": "MONDO:0002512", "names": ["Papillary adenocarcinoma", "papillary adenocarcinoma", "Papillary Adenocarcinoma", "adenocarcinoma papillary", "Adenocarcinoma, Papillary", "Papillary Adenocarcinomas", "Adenocarcinomas, Papillary", "Papillary adenocarcinoma NOS", "Papillary adenocarcinoma, NOS", "papillary adenocarcinoma (diagnosis)", "ADENOCARCINOMA, PAPILLARY, MALIGNANT", "adenocarcinoma, papillary, malignant", "infiltrating papillary adenocarcinoma", "Infiltrating Papillary Adenocarcinoma", "Infiltrating papillary adenocarcinoma", "infiltrating and papillary adenocarcinoma", "Infiltrating and papillary adenocarcinoma", "papillary adenocarcinoma (morphologic abnormality)", "Intraductal Papillary Adenocarcinoma with Invasion", "Intraductal papillary adenocarcinoma with invasion", "Papillary adenocarcinoma (morphologic abnormality)", "[M] Intraductal papillary adenocarcinoma with invasion", "papillary adenocarcinoma NOS (morphologic abnormality)", "Breast Papillary Ductal Carcinoma In Situ with Invasion", "Breast Intraductal Papillary Adenocarcinoma with Invasion", "Intraductal papillary adenocarcinoma with invasion (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papillary adenocarcinoma", "shortest_name_length": 24}
{"curie": "MONDO:0002726", "names": ["Mast cell nevus", "Skin Mastocytoma", "Mast cell naevus", "skin mastocytoma", "Mastocytoma, Skin", "Mastocytoma of skin", "Solitary mastocytoma", "Multiple mastocytoma", "Cutaneous mastocytoma", "Skin Solitary Mastocytoma", "skin solitary mastocytoma", "Mast cell nevus (disorder)", "neoplasm of mast cell nevus", "Mast cell nevus (diagnosis)", "Cutaneous local mastocytoma", "Solitary Mastocytoma of Skin", "Solitary mastocytoma of skin", "solitary mastocytoma of skin", "Solitary Mastocytoma of skin", "solitary cutaneous mastocytoma", "Solitary cutaneous mastocytoma", "Cutaneous Solitary Mastocytoma", "cutaneous solitary mastocytoma", "solitary mastocytoma of the skin", "Solitary Mastocytoma of the Skin", "Solitary cutaneous mastocytoma (disorder)", "solitary cutaneous mastocytoma (diagnosis)", "Solitary mastocytoma of skin (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous solitary mastocytoma", "shortest_name_length": 15}
{"curie": "MONDO:0020073", "names": ["adolescent-onset epilepsy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adolescent-onset epilepsy syndrome", "shortest_name_length": 34}
{"curie": "MONDO:0800092", "names": ["genetic inflammatory or rheumatoid-like osteoarthropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genetic inflammatory or rheumatoid-like osteoarthropathy", "shortest_name_length": 56}
{"curie": "UMLS:C2721670", "names": ["Ultrafiltration failure", "Peritoneal membrane failure", "Ultrafiltration failure (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ultrafiltration failure", "shortest_name_length": 23}
{"curie": "MONDO:0013889", "names": ["SOPH", "soph", "SOPH syndrome", "soph syndrome", "SOPH SYNDROME", "short stature-optic atrophy-Pelger-Huët anomaly syndrome", "Short stature-optic atrophy-Pelger-Huët anomaly syndrome", "short stature-optic atrophy-Pelger-HuC+t anomaly syndrome", "short stature, optic nerve atrophy, and Pelger-Huet anomaly", "SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY", "short stature with optic atrophy and Pelger-Huët anomaly syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short stature-optic atrophy-Pelger-HuC+t anomaly syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0016046", "names": ["familial clubfoot with or without associated lower limb anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial clubfoot with or without associated lower limb anomalies", "shortest_name_length": 65}
{"curie": "UMLS:C0270960", "names": ["congenital myopathy", "myopathy congenital", "Congenital myopathy", "Myopathy, congenital", "myopathy; congenital", "congenital; myopathy", "Congenital myopathies", "myopathies congenital", "congenital myopathies", "Congenital myopathy, NOS", "Congenital myopathy (disorder)", "congenital myopathies (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital myopathy (disorder)", "shortest_name_length": 19}
{"curie": "MONDO:0000643", "names": ["Benign Vulva Tumor", "benign vulva tumor", "benign vulvar tumor", "Benign Vulvar Tumor", "benign tumor of vulva", "Benign tumor of vulva", "vulva benign neoplasm", "Benign Vulva Neoplasm", "benign vulva neoplasm", "Benign Tumor of Vulva", "Benign tumour of vulva", "benign vulvar neoplasm", "Benign Vulvar Neoplasm", "vulvar neoplasm benign", "Benign Vulval Neoplasm", "vulvar benign neoplasm", "Benign vulval neoplasm", "benign vulval neoplasm", "Vulval neoplasms benign", "Benign Neoplasm of Vulva", "Benign neoplasm of vulva", "benign neoplasm of vulva", "benign tumor of the vulva", "Benign Tumor of the Vulva", "Benign neoplasm of pudendum", "Benign Neoplasm of the Vulva", "benign neoplasm of the vulva", "Benign neoplasm of vulva, NOS", "mammalian vulva benign neoplasm", "Benign neoplasm of vulva (disorder)", "benign neoplasm of vulva (diagnosis)", "Benign neoplasm of external female genitalia NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar benign neoplasm", "shortest_name_length": 18}
{"curie": "UMLS:C4288550", "names": ["Oropharyngeal Poorly Differentiated Carcinoma", "Poorly Differentiated Oropharyngeal Throat Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oropharyngeal Poorly Differentiated Carcinoma", "shortest_name_length": 45}
{"curie": "MONDO:0011959", "names": ["SS", "AFND", "Afnd", "PAAND", "Sweet", "Sweet disease", "Sweet Syndrome", "SWEET SYNDROME", "Sweet syndrome", "sweet syndrome", "Syndrome, Sweet", "sweets syndrome", "sweet's disease", "Sweets Syndrome", "Sweet's disease", "SWEET'S SYNDROME", "sweet's syndrome", "Sweet's Syndrome", "Sweet's syndrome", "Syndrome, Sweet's", "Gomm-button disease", "Gomm Button Disease", "Gomm button disease", "GOMM-BUTTON DISEASE", "Gomm-Button Disease", "Disease, Gomm-Button", "Disease, Gomm Button", "Sweet's syndrome (diagnosis)", "Febrile neutrophilic dermatosis", "febrile neutrophilic dermatosis", "dermatosis; febrile neutrophilic", "febrile neutrophilic; dermatosis", "acute febrile neutrophilic dermatosis", "Acute Febrile Neutrophilic Dermatosis", "Acute febrile neutrophilic dermatosis", "neutrophilic dermatosis, acute febrile", "Neutrophilic Dermatosis, Acute Febrile", "NEUTROPHILIC DERMATOSIS, ACUTE FEBRILE", "Febrile neutrophilic dermatosis [Sweet]", "Dermatosis, Neutrophilic, Febrile, Acute", "PYRIN-ASSOCIATED AUTOINFLAMMATORY DISEASE", "Acute febrile neutrophilic dermatosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sweet syndrome", "shortest_name_length": 2}
{"curie": "MONDO:0011711", "names": ["SLI2", "SPECIFIC LANGUAGE IMPAIRMENT 2", "specific language impairment 2", "specific language impairment QTL, 2", "SPECIFIC LANGUAGE IMPAIRMENT QUANTITATIVE TRAIT LOCUS ON CHROMOSOME 19", "specific language impairment quantitative trait locus on chromosome 19"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "specific language impairment 2", "shortest_name_length": 4}
{"curie": "MONDO:0020083", "names": ["immunodeficiency-associated lymphoproliferative disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency-associated lymphoproliferative disease", "shortest_name_length": 55}
{"curie": "MONDO:0400006", "names": ["botryomycosis", "pyoderma vegetans", "bacterial pseudomycosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "botryomycosis", "shortest_name_length": 13}
{"curie": "UMLS:C5419581", "names": ["Refractory Grade 1 Follicular Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Grade 1 Follicular Lymphoma", "shortest_name_length": 38}
{"curie": "UMLS:C0995195", "names": ["anoxia brain", "brain anoxia", "Brain Anoxia", "Anoxia, Brain", "cerebral anoxia", "Cerebral Anoxia", "Anoxia cerebral", "Cerebral anoxia", "ANOXIA CEREBRAL", "anoxia cerebral", "Anoxia of brain", "CEREBRAL ANOXIA", "anoxia; cerebral", "cerebral; anoxia", "Anoxia, Cerebral", "Anoxia of brain (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anoxia of brain", "shortest_name_length": 12}
{"curie": "UMLS:C5418578", "names": ["Skin Pleomorphic Lipoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin Pleomorphic Lipoma", "shortest_name_length": 23}
{"curie": "UMLS:C3273069", "names": ["Bile Duct Mucinous Cystic Neoplasm, Low Grade", "Bile Duct Mucinous Cystic Neoplasm, Low-Grade", "Bile Duct MCN with Low Grade Intraepithelial Neoplasia", "Bile Duct Mucinous Cystic Neoplasm with Low Grade Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bile Duct Mucinous Cystic Neoplasm, Low Grade", "shortest_name_length": 45}
{"curie": "MONDO:0017301", "names": ["pericardial and diaphragmatic defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pericardial and diaphragmatic defect", "shortest_name_length": 36}
{"curie": "MONDO:0100078", "names": ["resistant hypertension", "drug resistant hypertension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "resistant hypertension", "shortest_name_length": 22}
{"curie": "MONDO:0001667", "names": ["streptobacillus infection", "Streptobacillus infection", "Streptobacillus infections", "Streptobacillus infection NOS", "streptobacillus infectious disease", "Infection caused by Streptobacillus", "infection caused by streptobacillus", "Infection caused by Streptobacillus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "streptobacillus infectious disease", "shortest_name_length": 25}
{"curie": "UMLS:C2711256", "names": ["Low flow priapism", "Low-flow priapism", "Ischemic priapism", "Ischaemic priapism", "Veno-occlusive priapism", "Ischemic priapism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ischemic priapism", "shortest_name_length": 17}
{"curie": "MONDO:0004768", "names": ["Keratoconjunctivitis", "keratoconjunctivitis", "KERATOCONJUNCTIVITIS", "Keratoconjunctivitides", "Keratoconjunctivitis, NOS", "Keratoconjunctivitis (disorder)", "Unspecified keratoconjunctivitis", "keratoconjunctivitis (diagnosis)", "Keratoconjunctivitis, unspecified", "Superficial keratitis with conjunctivitis", "keratitis; superficial, with conjunctivitis", "superficial; keratitis, with conjunctivitis", "Superficial keratitis with conjunctivitis NOS", "Superficial keratitis with conjunctivitis, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratoconjunctivitis", "shortest_name_length": 20}
{"curie": "MONDO:0010898", "names": ["ETL1", "ADEAF", "ADLTE", "ADPEAF", "familial temporal lobe epilepsy 1", "epilepsy, familial temporal lobe 1", "epilepsy, familial temporal lobe, 1", "partial epilepsy with auditory aura", "Partial epilepsy with auditory aura", "familial temporal lobe epilepsy type 1", "partial epilepsy with auditory features", "Partial epilepsy with auditory features", "epilepsy, familial temporal lobe, type 1", "EPILEPSY, PARTIAL, WITH AUDITORY FEATURES", "epilepsy, partial, with auditory features", "Epilepsy, Partial, With Auditory Features", "Autosomal dominant lateral temporal lobe epilepsy", "Autosomal Dominant Lateral Temporal Lobe Epilepsy", "autosomal dominant lateral temporal lobe epilepsy", "Autosomal dominant epilepsy with auditory features", "autosomal dominant epilepsy with auditory features", "epilepsy, lateral temporal lobe, autosomal dominant", "EPILEPSY, LATERAL TEMPORAL LOBE, AUTOSOMAL DOMINANT", "Epilepsy, Lateral Temporal Lobe, Autosomal Dominant", "Autosomal dominant partial epilepsy with auditory features", "autosomal dominant partial epilepsy with auditory features", "Autosomal dominant epilepsy with auditory features (disorder)", "Autosomal dominant epilepsy with auditory features (diagnosis)", "temporal lobe epilepsy autosomal dominant with auditory features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Autosomal dominant epilepsy with auditory features", "shortest_name_length": 4}
{"curie": "UMLS:C0520577", "names": ["Urethral atrophy", "Urethral atrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urethral atrophy", "shortest_name_length": 16}
{"curie": "MONDO:0009050", "names": ["PITA4", "ACTHoma", "cush disease", "cush's disease", "Cushing Disease", "disease cushing", "cushing disease", "Cushing disease", "CUSHING DISEASE", "Disease, Cushing", "cushing diseases", "Corticotropinoma", "cushings disease", "Cushing's Disease", "CUSHING'S DISEASE", "cushings diseases", "Cushing's disease", "cushing's disease", "cushings's disease", "Cushing basophilism", "Corticotroph adenoma", "Corticotroph Adenoma", "corticotroph adenoma", "Corticotropic Adenoma", "Adenoma, Corticotroph", "Corticotroph Adenomas", "ACTH secreting adenoma", "Overproduction of ACTH", "Adenomas, Corticotroph", "adenoma, ACTH secreting", "Pituitary Cushing Disease", "Cushing disease, pituitary", "Pituitary Cushing Diseases", "Pituitary Cushing Syndrome", "Cushing Disease, Pituitary", "Overproduction of cortisol", "Pituitary Cushing syndrome", "CUSHING DISEASE, PITUITARY", "Corticotroph PitNET/Adenoma", "Cushing Diseases, Pituitary", "PITUITARY CUSHINGS SYNDROME", "Cushing Syndrome, Pituitary", "pituitary Cushing's syndrome", "Cushing's disease (diagnosis)", "Pituitary ACTH Hypersecretion", "ACTH Hypersecretion, Pituitary", "corticotroph pituitary adenoma", "Corticotroph pituitary adenoma", "Pituitary hyperadrenocorticism", "Hypersecretion, Pituitary ACTH", "Corticotroph adenoma (disorder)", "hypersecretion; ACTH, pituitary", "ACTH Producing Pituitary Adenoma", "Pituitary ACTH Secreting Adenoma", "ACTH-Producing Pituitary Adenoma", "ACTH producing pituitary adenoma", "ACTH Secreting Pituitary Adenoma", "Pituitary ACTH-Secreting Adenoma", "ACTH-secreting pituitary adenoma", "ACTH-producing pituitary adenoma", "ACTH-Secreting Pituitary Adenoma", "Pituitary hyperadrenal corticism", "ACTH-Secreting Pituitary Adenomas", "pituitary adenoma, ACTH-secreting", "PITUITARY ADENOMA, ACTH SECRETING", "Pituitary Adenoma, ACTH Secreting", "Pituitary Adenoma, ACTH-Secreting", "Pituitary Adenoma, ACTH-Producing", "ACTH-Producing Pituitary Adenomas", "Pituitary Adenomas, ACTH-Secreting", "Pituitary Adenomas, ACTH-Producing", "Pituitary dependent Cushing disease", "PITUITARY ADENOMA 4, ACTH-SECRETING", "ACTH Secreting Adenoma of Pituitary", "pituitary adenoma 4, ACTH-secreting", "Pituitary corticotroph micro-adenoma", "Pituitary corticotropic cell adenoma", "pituitary dependent Cushing syndrome", "Pituitary-Dependant Cushing Syndrome", "pituitary-dependent Cushing syndrome", "Pituitary-dependent Cushing syndrome", "Pituitary dependent hypercortisolism", "Pituitary-Dependant Hypercortisolism", "pituitary corticotroph micro-adenoma", "Pituitary Dependant Hypercortisolism", "Pituitary Dependant Cushing Syndrome", "Pituitary-dependent Cushing's disease", "Cushing Syndrome, Pituitary-Dependant", "Hypercortisolism, Pituitary-Dependant", "Pituitary-Dependant Hypercortisolisms", "ACTH Producing Pituitary Gland Adenoma", "ACTH-Producing Pituitary Gland Adenoma", "Pituitary Gland ACTH-Secreting Adenoma", "Pituitary-dependent Cushing's syndrome", "ACTH Secreting Adenoma of the Pituitary", "Cushing disease due to pituitary adenoma", "Pituitary dependent hyperadrenocorticism", "Pituitary Corticotropin-Secreting Adenoma", "Hyperadrenocorticism, pituitary dependent", "hyperadrenocorticism; pituitary-dependent", "Corticotropin-secreting pituitary adenoma", "pituitary-dependent; hyperadrenocorticism", "Pituitary Corticotropin Secreting Adenoma", "Corticotropin-Secreting Adenoma, Pituitary", "Pituitary Corticotropin-Secreting Adenomas", "Corticotropin-Secreting Adenomas, Pituitary", "Corticotroph Pituitary Neuroendocrine Tumor", "ACTH-secreting pituitary adenoma (diagnosis)", "pituitary adenoma 4, ACTH-secreting, somatic", "BRAIN TUMOR, ACTH SECRETING PITUITARY ADENOMA", "Pituitary-Dependant Hypercortisolism Disorder", "Pituitary Dependant Hypercortisolism Disorder", "Hypercortisolism Disorder, Pituitary-Dependant", "Pituitary-Dependant Hypercortisolism Disorders", "Corticotropin Secreting Pituitary Gland Adenoma", "Adrenocorticotropin Producing Pituitary Adenoma", "Adrenocorticotropin Secreting Pituitary Adenoma", "Pituitary-dependent Cushing's disease (disorder)", "Corticotropin Secreting Adenoma of the Pituitary", "Cushing; syndrome or disease, pituitary-dependent", "Adrenocorticotropin Producing Adenoma of Pituitary", "Adrenocorticotropin Secreting Adenoma of Pituitary", "Corticotroph Pituitary Neuroendocrine Tumor/Adenoma", "Adrenocorticotropin Producing Pituitary Gland Adenoma", "Adrenocorticotropin Secreting Pituitary Gland Adenoma", "Adrenocorticotropin Secreting Adenoma of the Pituitary", "Adrenocorticotropin Producing Adenoma of the Pituitary", "INTRACRANIAL NEOPLASM, ACTH SECRETING PITUITARY ADENOMA", "ACTH producing pituitary hyperplasia (Cushing's disease)", "Adrenocorticotropin Secreting Adenoma of Pituitary Gland", "Adrenocorticotropin Producing Adenoma of Pituitary Gland", "ACTH producing ('basophilic') adenoma (Cushing's disease)", "Adrenocorticotropin Producing Adenoma of the Pituitary Gland", "Adrenocorticotropin Secreting Adenoma of the Pituitary Gland", "adrenocorticotropic hormone producing pituitary hyperplasia (Cushing's disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cushing disease due to pituitary adenoma", "shortest_name_length": 5}
{"curie": "MONDO:0001701", "names": ["GI anthrax", "anthrax gastrointestinal", "Gastrointestinal anthrax", "gastrointestinal anthrax", "anthrax; gastrointestinal", "gastrointestinal; anthrax", "Gastrointestinal anthrax (disorder)", "gastrointestinal anthrax (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastrointestinal anthrax", "shortest_name_length": 10}
{"curie": "UMLS:C0855157", "names": ["Primary mediastinal large B-cell lymphoma stage III", "Primary Mediastinal Large B-Cell Lymphoma Stage III", "Stage III Primary Mediastinal Large B-Cell Lymphoma", "Stage III Mediastinal (Thymic) Large B-Cell Lymphoma", "Ann Arbor Stage III Primary Mediastinal (Thymic) Large B-Cell Lymphoma", "Large B-cell lymphoma subtype primary mediastinal (Thymic) large B-cell lymphoma stage III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary mediastinal large B-cell lymphoma stage III", "shortest_name_length": 51}
{"curie": "MONDO:0027026", "names": ["GCBL", "Giant Condyloma", "Giant acuminate warts", "Buschke Löwenstein Tumor", "Buschke-Lowenstein tumor", "Buschke Lowenstein Tumor", "Buschke-Lowenstein Tumor", "Buschke Lowenstein tumor", "Buschke-Löwenstein Tumor", "Buschke-Lowenstein tumour", "Giant condyloma acuminata", "tumor, Buschke-Lowenstein", "Tumor, Buschke Lowenstein", "Löwenstein Tumor, Buschke", "tumor, Buschke Lowenstein", "Lowenstein Tumor, Buschke", "Tumor, Buschke-Löwenstein", "Lowenstein tumor, Buschke", "Tumor, Buschke-Lowenstein", "Tumor, Buschke Löwenstein", "Buschke-Lowenstein's tumor", "Giant condyloma acuminatum", "Giant Condyloma Acuminatum", "Giant condyloma Acuminatum", "Condyloma Acuminatum, Giant", "Buschke-Lowenstein's tumour", "Buschke-Lowenstein Neoplasm", "Giant condyloma Acuminatums", "condyloma Acuminatum, Giant", "Giant Condyloma Acuminatums", "condyloma Acuminatums, Giant", "Condyloma Acuminatums, Giant", "Buschke-Löwenstein tumor of penis", "Buschke-Löwenstein giant condyloma", "Buschke-Lowenstein giant condyloma", "Buschke-Löwenstein tumour of penis", "Anogenital Type Verrucous Carcinoma", "anogenital type verrucous carcinoma", "Giant Condyloma of Buschke and Löwenstein", "Giant condyloma of Buschke and Lowenstein", "Giant Condyloma of Buschke and Lowenstein", "giant condyloma of Buschke and Lowenstein", "Penile verrucous carcinoma of Buschke-Lowenstein", "Penile verrucous carcinoma of Buschke-Löwenstein", "Verrucous carcinoma of penis (Buschke-Löwenstein)", "Anogenital verrucous carcinoma of Buschke-Lowenstein", "Anogenital verrucous carcinoma of Buschke-Löwenstein", "Penile verrucous carcinoma of Buschke-Löwenstein (disorder)", "Anogenital verrucous carcinoma of Buschke-Löwenstein (disorder)", "giant condyloma acuminatum involving the prepuce and glans penis", "Anogenital verrucous carcinoma of Buschke-Lowenstein (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Buschke Lowenstein tumor", "shortest_name_length": 4}
{"curie": "UMLS:C1096340", "names": ["Dysphemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dysphemia", "shortest_name_length": 9}
{"curie": "UMLS:C0280388", "names": ["Stage I Epidermoid Carcinoma of Hypopharynx", "Stage I Hypopharyngeal Epidermoid Carcinoma", "hypopharynx squamous cell carcinoma, stage I", "Stage I Hypopharyngeal Squamous Cell Carcinoma", "Hypopharyngeal squamous cell carcinoma stage I", "Stage I Squamous Cell Carcinoma of Hypopharynx", "Stage I Epidermoid Carcinoma of the Hypopharynx", "hypopharyngeal squamous cell carcinoma, stage I", "epidermoid carcinoma of the hypopharynx, stage I", "stage I squamous cell carcinoma of the hypopharynx", "Stage I Hypopharyngeal Throat Squamous Cell Cancer", "Squamous cell carcinoma of the hypopharynx stage I", "Stage I Squamous Cell Carcinoma of the Hypopharynx", "squamous cell carcinoma of the hypopharynx, stage I", "Stage I Hypopharyngeal Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypopharyngeal squamous cell carcinoma stage I", "shortest_name_length": 43}
{"curie": "UMLS:C0279746", "names": ["adenocarcinoma salivary gland", "Salivary gland adenocarcinoma", "Salivary Gland Adenocarcinoma", "salivary gland adenocarcinoma", "adenocarcinoma, salivary gland", "adenocarcinoma glands salivary", "adenocarcinoma of salivary gland", "Adenocarcinoma of salivary gland", "Adenocarcinoma of Salivary Gland", "Adenocarcinoma of the Salivary Gland", "Adenocarcinoma of salivary gland (disorder)", "adenocarcinoma of salivary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma of salivary gland", "shortest_name_length": 29}
{"curie": "MONDO:0010976", "names": ["EBS1D", "EBSB1", "EBS-AR KRT14", "EBS, autosomal recessive K14", "KRT14-related autosomal recessive EBS", "KRT14-related epidermolysis bullosa simplex", "Autosomal recessive epidermolysis bullosa simplex", "Epidermolysis Bullosa Simplex, Autosomal Recessive", "epidermolysis bullosa simplex, autosomal recessive 1", "epidermolysis bullosa simplex, autosomal recessive K14", "epidermolysis bullosa simplex, autosomal recessive type 1", "Autosomal recessive epidermolysis bullosa simplex (disorder)", "EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE (disorder)", "KRT14-related autosomal recessive epidermolysis bullosa simplex", "epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive", "EPIDERMOLYSIS BULLOSA SIMPLEX 1D, GENERALIZED, INTERMEDIATE OR SEVERE, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive", "shortest_name_length": 5}
{"curie": "UMLS:C0155778", "names": ["varicose veins leg", "leg varicose veins", "Varicose veins;leg", "legs varicose veins", "Varicose veins, leg", "Varicose veins of leg", "Varicose veins of legs", "Leg(s) Varicose Vein(s)", "Varix of lower extremity", "varicose veins on the leg", "VV - Varicose veins of leg", "Varix of lower extremities", "Varicose veins of lower limb", "Varix of lower extremity, NOS", "Phlebectasia of lower extremity", "extremities lower varicose vein", "extremities lower varicose veins", "Phlebectasia of lower extremities", "Varicose veins of lower extremity", "Varicose Vein of Lower Extremities", "varicose veins of lower extremities", "Varicose veins of lower extremities", "Phlebectasia of lower extremity, NOS", "Varicose veins of legs (excluding S97)", "Varicose veins of lower extremity, NOS", "varicose veins of the leg (non-specific)", "Varicose veins of lower extremity (disorder)", "varicose veins of lower extremities (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Varicose veins of lower extremity", "shortest_name_length": 18}
{"curie": "UMLS:C0862792", "names": ["Stage IIIA Lung Adenocarcinoma", "Adenocarcinoma of lung stage IIIA", "Stage IIIA Adenocarcinoma of Lung", "Stage IIIA Adenocarcinoma of the Lung", "Stage IIIA Lung Adenocarcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenocarcinoma of lung stage IIIA", "shortest_name_length": 30}
{"curie": "UMLS:C4527328", "names": ["Recurrent Central Nervous System Lymphoma", "Recurrent Primary Central Nervous System Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Central Nervous System Lymphoma", "shortest_name_length": 41}
{"curie": "MONDO:0019816", "names": ["anomaly of the tricuspid subvalvular apparatus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anomaly of the tricuspid subvalvular apparatus", "shortest_name_length": 46}
{"curie": "MONDO:0000871", "names": ["Childhood T-ALL", "childhood T-ALL", "T-Cell Childhood ALL", "T-cell pediatric ALL", "T-cell childhood ALL", "T cell pediatric ALL", "T-Cell Pediatric ALL", "T cell childhood ALL", "T cell ALL, childhood", "childhood ALL, T cell", "pediatric ALL, T cell", "T-cell ALL, pediatric", "childhood ALL, T-cell", "pediatric ALL, T-cell", "T cell ALL, pediatric", "ALL, childhood T-cell", "T-cell ALL, childhood", "ALL, pediatric T-cell", "T Acute Lymphoblastic Leukemia", "T acute lymphoblastic leukemia", "Childhood T-Acute Lymphoblastic Leukemia", "childhood T acute lymphoblastic leukemia", "Childhood T Acute Lymphoblastic Leukemia", "T-cell pediatric acute lymphocytic leukemia", "T-cell childhood acute lymphocytic leukemia", "T cell pediatric acute lymphocytic leukemia", "T-Cell Childhood Acute Lymphocytic Leukemia", "T-Cell Pediatric Acute Lymphocytic Leukemia", "T-cell acute lymphocytic leukemia, childhood", "Childhood Precursor T-Lymphoblastic Leukemia", "leukemia, childhood acute lymphocytic T-cell", "T cell acute lymphocytic leukemia, childhood", "pediatric acute lymphocytic leukemia, T-cell", "childhood acute lymphocytic leukemia, T-cell", "acute lymphocytic leukemia, childhood T-cell", "childhood precursor T-lymphoblastic leukemia", "leukemia, pediatric acute lymphocytic T-cell", "childhood T-cell acute lymphoblastic leukemia", "T-cell pediatric acute lymphoblastic leukemia", "Childhood T-Cell Acute Lymphoblastic Leukemia", "T-Cell Childhood Acute Lymphoblastic Leukemia", "T-Cell Pediatric Acute Lymphoblastic Leukemia", "T-cell childhood acute lymphoblastic leukemia", "childhood acute lymphoblastic leukemia, T-cell", "acute lymphoblastic leukemia, childhood T-cell", "childhood precursor T-lymphoblastic lymphoma/leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-cell childhood acute lymphocytic leukemia", "shortest_name_length": 15}
{"curie": "UMLS:C4527187", "names": ["Stage IIIC", "Stage IIIC Cutaneous (Skin) Melanoma", "Pathologic Stage IIIC Cutaneous Melanoma AJCC v8", "Pathologic Stage IIIC Melanoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IIIC Cutaneous Melanoma AJCC v8", "shortest_name_length": 10}
{"curie": "MONDO:0035824", "names": ["KLHL7-related Crisponi-like syndrome", "KLHL7-related cold-induced sweating-like syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "KLHL7-related cold-induced sweating-like syndrome", "shortest_name_length": 36}
{"curie": "UMLS:C1328447", "names": ["Brain stem syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brain stem syndrome", "shortest_name_length": 19}
{"curie": "MONDO:0004527", "names": ["congenital granular cell tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital granular cell tumor", "shortest_name_length": 30}
{"curie": "UMLS:C4553569", "names": ["Stage III Ovarian Cancer", "Stage III Ovarian Cancer AJCC v8", "Stage III Ovarian Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Ovarian Cancer AJCC v8", "shortest_name_length": 24}
{"curie": "UMLS:C0457520", "names": ["Dentinoma", "dentinoma", "Ameloblastic fibrodentinoma", "Ameloblastic Fibrodentinoma", "Ameloblastic fibrodentinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ameloblastic fibrodentinoma", "shortest_name_length": 9}
{"curie": "MONDO:0003991", "names": ["Endometrioid adenocarcinoma, villoglandular", "Villoglandular Endometrial Endometrioid Adenocarcinoma", "villoglandular endometrial endometrioid adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "villoglandular endometrial endometrioid adenocarcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0015715", "names": ["severe hemophilia B", "severe hemophilia type B", "severe factor IX deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe hemophilia B", "shortest_name_length": 19}
{"curie": "MONDO:0015828", "names": ["uterovaginal malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterovaginal malformation", "shortest_name_length": 25}
{"curie": "MONDO:0010271", "names": ["Xq28 contiguous gene deletion syndrome", "myotubular myopathy with abnormal genital development", "MYOTUBULAR MYOPATHY WITH ABNORMAL GENITAL DEVELOPMENT", "Myotubular Myopathy with Abnormal Genital Development", "X-linked myotubular myopathy-abnormal genitalia syndrome", "X-linked myotubular myopathy, abnormal genitalia syndrome", "X-linked myotubular myopathy, abnormal genitalia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked myotubular myopathy-abnormal genitalia syndrome", "shortest_name_length": 38}
{"curie": "UMLS:C2931517", "names": ["Anaplastic Plasmacytoma", "Plasmacytoma anaplastic", "Anaplastic skeletal plasmacytoma (type)", "Extramedullary anaplastic plasmacytoma (type)", "Anaplastic solitary extramedullary plasmacytoma of the cecum (type)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Plasmacytoma anaplastic", "shortest_name_length": 23}
{"curie": "UMLS:C5206683", "names": ["Unresectable Fibrolamellar Carcinoma", "Unresectable Fibrolamellar Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Fibrolamellar Carcinoma", "shortest_name_length": 36}
{"curie": "UMLS:C1335451", "names": ["Posterior Pharyngeal Wall Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Posterior Pharyngeal Wall Squamous Cell Carcinoma", "shortest_name_length": 49}
{"curie": "MONDO:0100192", "names": ["FAILURE LIVER", "liver failure", "failure liver", "Failure liver", "LIVER FAILURE", "Liver failure", "Liver Failure", "Liver--Failure", "Failure;hepatic", "Hepatic failure", "failure hepatic", "hepatic failure", "Hepatic Failure", "HEPATIC FAILURE", "Liver Insufficiency", "Insufficiency, Liver", "Liver decompensation", "liver decompensation", "Hepatic failure, NOS", "HEPATIC INSUFFICIENCY", "hepatic insufficiency", "Hepatic Insufficiency", "insufficiency hepatic", "Hepatic insufficiency", "liver function failure", "Insufficiency, Hepatic", "insufficiency; hepatic", "hepatic; insufficiency", "Liver function failure", "Liver decompensation, NOS", "Hepatic failure (disorder)", "Hepatic insufficiency, NOS", "hepatic failure (diagnosis)", "Liver function failure, NOS", "Hepatic failure, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "liver failure", "shortest_name_length": 13}
{"curie": "MONDO:0032644", "names": ["EV3", "epidermodysplasia verruciformis 3", "epidermodysplasia verruciformis, susceptibility to, 3", "EPIDERMODYSPLASIA VERRUCIFORMIS, SUSCEPTIBILITY TO, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermodysplasia verruciformis, susceptibility to, 3", "shortest_name_length": 3}
{"curie": "UMLS:C1112175", "names": ["Factor V inhibition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Factor V inhibition", "shortest_name_length": 19}
{"curie": "MONDO:0019675", "names": ["SEMDJL", "SEMDJL1", "SEMD-JL", "spondyloepimetaphyseal dysplasia joint laxity", "Spondyloepimetaphyseal Dysplasia With Joint Laxity", "spondyloepimetaphyseal dysplasia with joint laxity", "Spondyloepimetaphyseal dysplasia with joint laxity", "spondyloepimetaphyseal dysplasia with joint laxity type 1", "Spondyloepimetaphyseal dysplasia with joint laxity (disorder)", "spondyloepimetaphyseal dysplasia with joint laxity, Beighton type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepimetaphyseal dysplasia with joint laxity", "shortest_name_length": 6}
{"curie": "UMLS:C4521652", "names": ["IIB", "Stage IIB Esophageal Adenocarcinoma", "Pathologic Stage IIB Esophageal Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IIB Esophageal Adenocarcinoma AJCC v8", "shortest_name_length": 3}
{"curie": "MONDO:0014470", "names": ["DFNA65", "autosomal dominant deafness 65", "DEAFNESS, AUTOSOMAL DOMINANT 65", "deafness, autosomal dominant 65", "deafness, autosomal dominant type 65", "autosomal dominant nonsyndromic deafness 65", "autosomal dominant nonsyndromic hearing loss 65", "autosomal dominant nonsyndromic deafness type 65", "TBC1D24 autosomal dominant nonsyndromic deafness", "autosomal dominant nonsyndromic deafness caused by mutation in TBC1D24"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 65", "shortest_name_length": 6}
{"curie": "MONDO:0022982", "names": ["die Smulders Vles Fryns syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "die Smulders Vles Fryns syndrome", "shortest_name_length": 32}
{"curie": "MONDO:0001715", "names": ["a.basilaris; occlusion", "occlusion basilar artery", "Basilar artery occlusion", "basilar artery occlusion", "occlusion; basilar artery", "Basilar artery obstruction", "obstruction; basilar artery", "Occlusion of basilar artery", "Basilar artery occlusion (disorder)", "basilar artery occlusion (diagnosis)", "Occlusion and stenosis of basilar artery"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "basilar artery occlusion", "shortest_name_length": 22}
{"curie": "UMLS:C0235922", "names": ["Benign neoplasm breast", "Neoplasm benign;breast;F", "Benign Female Breast Tumor", "Benign Tumor of Female Breast", "Benign neoplasm breast female", "BREAST NEOPLASM BENIGN FEMALE", "benign tumor of female breast", "Breast neoplasm benign female", "benign female breast neoplasm", "Benign Female Breast Neoplasm", "Benign neoplasm of female breast", "Benign Neoplasm of Female Breast", "benign neoplasm of female breast", "Benign Tumor of the Female Breast", "benign neoplasm of the female breast", "Benign Neoplasm of the Female Breast", "Benign neoplasm of female breast, NOS", "Benign neoplasm breast (excluding X88)", "Benign neoplasm of female breast (disorder)", "benign neoplasm of female breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign neoplasm of female breast", "shortest_name_length": 22}
{"curie": "UMLS:C1332610", "names": ["Brainstem Glioblastoma", "Brain Stem Glioblastoma", "Glioblastoma Multiforme", "Brainstem Glioblastoma Multiforme", "Brain Stem Glioblastoma Multiforme", "Glioblastoma Multiforme of Brainstem", "Glioblastoma Multiforme of Brain Stem", "Glioblastoma Multiforme of the Brainstem", "Glioblastoma Multiforme of the Brain Stem"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brain Stem Glioblastoma", "shortest_name_length": 22}
{"curie": "MONDO:0043003", "names": ["acanthosis nigricans", "Familial acanthosis nigricans", "familial acanthosis nigricans", "hereditary acanthosis nigricans (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial acanthosis nigricans", "shortest_name_length": 20}
{"curie": "MONDO:0002883", "names": ["intestine NET", "intestine neuroendocrine tumor", "neuroendocrine tumor of Intestine", "neuroendocrine tumor of intestine", "intestine neuroendocrine neoplasm", "Intestinal Neuroendocrine Neoplasm", "intestinal neuroendocrine neoplasm", "neuroendocrine tumour of Intestine", "Neuroendocrine Neoplasm of Intestine", "neuroendocrine neoplasm of intestine", "intestinal neuroendocrine benign tumor", "intestinal neuroendocrine benign tumour", "Neuroendocrine Neoplasm of the Intestine", "neuroendocrine neoplasm of the intestine", "intestine neuroendocrine tumor, well differentiated, low or intermediate grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intestinal neuroendocrine neoplasm", "shortest_name_length": 13}
{"curie": "UMLS:C0853327", "names": ["Penile size reduced"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Penile size reduced", "shortest_name_length": 19}
{"curie": "MONDO:0006767", "names": ["gave", "Watermelon Stomach", "watermelon stomach", "Watermelon stomach", "Stomach, Watermelon", "Watermelon Stomachs", "Stomachs, Watermelon", "Antral Vascular Ectasia", "Antral Vascular Ectasias", "Ectasia, Antral Vascular", "Vascular Ectasia, Antral", "Ectasias, Antral Vascular", "Vascular Ectasias, Antral", "Gastric antral vascular ectasia", "Gastric Antral Vascular Ectasia", "gastric antral vascular ectasia", "antral ectasias gastric vascular", "Vascular ectasia of gastric antrum", "vascular ectasia of gastric antrum", "GAVE - Gastric antral vascular ectasia", "GAVE (gastric antral vascular ectasia)", "Vascular ectasia of gastric antrum (disorder)", "vascular ectasia of gastric antrum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastric antral vascular ectasia", "shortest_name_length": 4}
{"curie": "MONDO:0016272", "names": ["endometrial transitional cell carcinoma", "body of uterus transitional cell carcinoma", "transitional cell carcinoma of the corpus uteri"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transitional cell carcinoma of the corpus uteri", "shortest_name_length": 39}
{"curie": "UMLS:C4528571", "names": ["Stage I Breast Cancer", "Prognostic Stage I Breast Cancer AJCC v8", "Prognostic Stage I Breast Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prognostic Stage I Breast Cancer AJCC v8", "shortest_name_length": 21}
{"curie": "UMLS:C3896961", "names": ["Pre-B Acute Lymphoblastic Leukemia", "Adult Pre-B Acute Lymphoblastic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Pre-B Acute Lymphoblastic Leukemia", "shortest_name_length": 34}
{"curie": "MONDO:0009555", "names": ["malocclusion and short stature", "Malocclusion and Short Stature", "MALOCCLUSION AND SHORT STATURE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malocclusion and short stature", "shortest_name_length": 30}
{"curie": "MONDO:0002222", "names": ["urethra leiomyoma", "Urethra Leiomyoma", "urethral leiomyoma", "Urethral Leiomyoma", "Leiomyoma of Urethra", "leiomyoma of urethra", "leiomyoma of the urethra", "Leiomyoma of the Urethra"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urethra leiomyoma", "shortest_name_length": 17}
{"curie": "MONDO:0700136", "names": ["bovine protoporphyria", "Bovine Protoporphyria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bovine protoporphyria", "shortest_name_length": 21}
{"curie": "OMIM:136150", "names": ["FLOOD FACTOR DEFICIENCY", "Flood Factor Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 23}
{"curie": "MONDO:0009097", "names": ["RNANC", "NCRNA", "PHPVAR", "persistent fetal vasculature", "Detachment of Retina, Congenital", "RETINAL NONATTACHMENT AND FALCIFORM DETACHMENT", "retinal nonattachment and falciform detachment", "Retinal Nonattachment, Nonsyndromic Congenital", "Retinal Nonattachment And Falciform Detachment", "retinal nonattachment, nonsyndromic congenital", "RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL", "autosomal recessive persistent hyperplastic primary vitreous", "Persistent Hyperplastic Primary Vitreous, Autosomal Recessive", "persistent hyperplastic primary vitreous, autosomal recessive", "PERSISTENT HYPERPLASTIC PRIMARY VITREOUS, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "persistent hyperplastic primary vitreous, autosomal recessive", "shortest_name_length": 5}
{"curie": "UMLS:C5239282", "names": ["Unresectable Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Neuroendocrine Neoplasm", "shortest_name_length": 36}
{"curie": "UMLS:C0009760", "names": ["CONJUNCTIVAL BLEEDING", "Conjunctival bleeding", "Conjunctiva hemorrhage", "conjunctiva hemorrhage", "Conjunctival hemorrhage", "haemorrhage conjunctiva", "CONJUNCTIVAL HEMORRHAGE", "conjunctival hemorrhage", "Conjunctiva haemorrhage", "hemorrhage; conjunctiva", "conjunctiva; hemorrhage", "Conjunctival Hemorrhage", "Conjunctival haemorrhage", "CONJUNCTIVAL HAEMORRHAGE", "conjunctival hemorrhages", "conjunctival haemorrhage", "Conjunctival hemorrhage (disorder)", "Conjunctival hemorrhage, unspecified eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conjunctival hemorrhage", "shortest_name_length": 21}
{"curie": "MONDO:0014108", "names": ["FANCQ", "ERCC4 Fanconi anemia", "Fanconi anemia complementation group Q", "Fanconi anemia, complementation group Q", "FANCONI ANEMIA, COMPLEMENTATION GROUP Q", "Fanconi anemia caused by mutation in ERCC4", "Fanconi anemia complementation group type Q", "Fanconi Anemia, complementation group type Q"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fanconi anemia complementation group Q", "shortest_name_length": 5}
{"curie": "UMLS:C4682654", "names": ["Gestational Trophoblastic Tumor by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gestational Trophoblastic Tumor by AJCC v7 Stage", "shortest_name_length": 48}
{"curie": "MONDO:0024237", "names": ["genetic neurodegenerative disease", "Neurodegenerative Hereditary Disease", "inherited neurodegenerative disorder", "hereditary neurodegenerative disease", "Hereditary Neurodegenerative Disease", "Neurodegenerative Disease, Hereditary", "Hereditary Disease, Neurodegenerative", "Disease, Hereditary Neurodegenerative", "Disease, Neurodegenerative Hereditary", "Hereditary Neurodegenerative Diseases", "Neurodegenerative Hereditary Diseases", "hereditary neurodegenerative disorder", "Hereditary Neurodegenerative Disorder", "Neurodegenerative Diseases, Hereditary", "Diseases, Hereditary Neurodegenerative", "Hereditary Diseases, Neurodegenerative", "Diseases, Neurodegenerative Hereditary", "Heredodegenerative Disorders, Nervous System", "Nervous System Hereditary Degenerative Diseases", "Nervous System Degenerative Hereditary Diseases", "Degenerative Disease, Nervous System, Hereditary", "Degenerative Hereditary Diseases, Nervous System", "Nervous System Diseases, Degenerative, Hereditary", "Hereditary-Degenerative Disorders, Nervous System", "Degenerative Hereditary Disorders, Nervous System", "Hereditary Degenerative Disorders, Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited neurodegenerative disorder", "shortest_name_length": 33}
{"curie": "MONDO:0015199", "names": ["Walker Dyson syndrome", "Walker-Dyson syndrome", "Aniridia-intellectual disability syndrome", "aniridia - intellectual disability syndrome", "Aniridia and intellectual disability syndrome", "aniridia and intellectual disability syndrome", "Aniridia and intellectual disability syndrome (disorder)", "aniridia and intellectual disability syndrome (diagnosis)", "aniridia associated with mental retardation and other eye abnormalities", "Aniridia associated with mental retardation and other eye abnormalities", "aniridia associated with intellectual disability and other eye abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aniridia - intellectual disability syndrome", "shortest_name_length": 21}
{"curie": "MONDO:0007674", "names": ["G6PDL", "glucose-6-phosphate dehydrogenase-like", "GLUCOSE-6-PHOSPHATE DEHYDROGENASE-LIKE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glucose-6-phosphate dehydrogenase-like", "shortest_name_length": 5}
{"curie": "UMLS:C4683631", "names": ["St. Jude Stage III Childhood Non-Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "St. Jude Stage III Childhood Non-Hodgkin Lymphoma AJCC v8", "shortest_name_length": 57}
{"curie": "MONDO:0012714", "names": ["SALMY", "EOMFC", "Salih Cmd", "Salih myopathy", "SALIH MYOPATHY", "Salih Myopathy", "congenital myopathy 5", "Salih congenital muscular dystrophy", "Salih Congenital Muscular Dystrophy", "congenital myopathy-5 with cardiomyopathy", "Early-Onset Myopathy with Fatal Cardiomyopathy", "Early onset myopathy with fatal cardiomyopathy", "Early-onset myopathy with fatal cardiomyopathy", "early-onset myopathy with fatal cardiomyopathy", "Myopathy, Early-Onset, with Fatal Cardiomyopathy", "myopathy, early-onset, with fatal cardiomyopathy", "MYOPATHY, EARLY-ONSET, WITH FATAL CARDIOMYOPATHY", "Early onset myopathy with fatal cardiomyopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early-onset myopathy with fatal cardiomyopathy", "shortest_name_length": 5}
{"curie": "UMLS:C0750917", "names": ["Auditory Discriminatory Aphasia", "Discriminatory Aphasia, Auditory", "Aphasia, Auditory Discriminatory", "Auditory Discriminatory Aphasias", "Discriminatory Aphasias, Auditory"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aphasia, Auditory Discriminatory", "shortest_name_length": 31}
{"curie": "UMLS:C3267094", "names": ["Infected fistula"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infected fistula", "shortest_name_length": 16}
{"curie": "MONDO:0018720", "names": ["common cystic lymphatic malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "common cystic lymphatic malformation", "shortest_name_length": 36}
{"curie": "MONDO:0022609", "names": ["Bronchial carcinoid", "bronchial carcinoids", "bronchial adenomas/carcinoids childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bronchial adenomas/carcinoids childhood", "shortest_name_length": 19}
{"curie": "MONDO:0017055", "names": ["MMF embryopathy", "mycophenolate mofetil embryopathy", "Mycophenolate mofetil embryopathy", "Embryopathy caused by mycophenolate mofetil", "Embryopathy caused by mycophenolate mofetil (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mycophenolate mofetil embryopathy", "shortest_name_length": 15}
{"curie": "MONDO:0018369", "names": ["immature teratoma", "Grade 2 Ovarian Teratoma", "ovary malignant teratoma", "Ovarian Immature Teratoma", "immature ovarian teratoma", "ovarian immature teratoma", "Ovarian immature teratoma", "Immature Ovarian Teratoma", "immature teratoma of ovary", "Ovarian malignant teratoma", "Immature Teratoma of Ovary", "malignant ovarian teratoma", "immature teratoma, ovarian", "ovarian malignant teratoma", "Malignant Ovarian Teratoma", "Immature teratoma of ovary", "teratoma, immature, ovarian", "Malignant Teratoma of Ovary", "malignant teratoma of ovary", "Malignant teratoma of ovary", "malignant teratoma of Ovary", "immature teratoma of the ovary", "Immature Teratoma of the Ovary", "Malignant Teratoma of the Ovary", "malignant teratoma of the ovary", "Ovarian Germ Cell Immature Teratoma", "ovarian immature germ cell teratoma", "ovarian germ cell immature teratoma", "Ovarian Immature Germ Cell Teratoma", "malignant ovarian germ cell teratoma", "Immature Germ Cell Teratoma of Ovary", "Malignant Ovarian Germ Cell Teratoma", "immature germ cell teratoma of ovary", "Malignant Germ Cell Teratoma of Ovary", "malignant germ cell teratoma of ovary", "Immature teratoma of ovary (diagnosis)", "malignant teratoma of ovary (diagnosis)", "Immature Germ Cell Teratoma of the Ovary", "immature germ cell teratoma of the ovary", "malignant germ cell teratoma of the ovary", "Malignant Germ Cell Teratoma of the Ovary", "ovarian neoplasm malignant immature teratoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immature ovarian teratoma", "shortest_name_length": 17}
{"curie": "MONDO:0018740", "names": ["Acquired Methemoglobinemia", "Acquired methemoglobinemia", "acquired methemoglobinemia", "Methemoglobinemia, acquired", "acquired; methemoglobinemia", "methemoglobinemia; acquired", "Acquired methaemoglobinaemia", "drug induced methemoglobinemia", "Drug-Induced Methemoglobinemia", "Drug Induced Methemoglobinemia", "Drug-induced methemoglobinemia", "drug-induced methemoglobinemia", "Drug-induced methaemoglobinaemia", "Acquired methemoglobinemia (disorder)", "Drug-induced methemoglobinemia (disorder)", "drug-induced methemoglobinemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "drug-induced methemoglobinemia", "shortest_name_length": 26}
{"curie": "UMLS:C0280099", "names": ["Solid Tumor", "adult solid tumor", "Adult Solid Tumor", "solid tumor, adult", "Adult Solid Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Solid Neoplasm", "shortest_name_length": 11}
{"curie": "MONDO:0018633", "names": ["Del(20)(q11.2)", "monosomy 20q11", "20q11.2 microdeletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "20q11.2 microdeletion syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0015317", "names": ["Laryngotracheal angioma", "laryngotracheal angioma", "Laryngotracheal hemangioma", "Laryngotracheal haemangioma", "Laryngotracheal hemangioma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laryngotracheal angioma", "shortest_name_length": 23}
{"curie": "MONDO:0005706", "names": ["DESERT FEVER", "desert fever", "Valley Fever", "Desert fever", "Valley fever", "Valley Fevers", "FEVER, VALLEY", "FEVER, DESERT", "Posada-Wernicke", "Wernicke-Posada", "Desert rheumatism", "desert rheumatism", "COCCIDIOIDOMYCOSIS", "California disease", "Coccidioidomycoses", "coccidioidomycosis", "FEVER, SAN JOAQUIN", "Coccidioidomycosis", "Coccidioides infection", "disease posada wernicke", "Coccidioidomycosis, NOS", "San Joaquin valley fever", "San Joaquin Valley fever", "Posadas-Wernicke disease", "San Joaquin Valley Fever", "POSADAS-WERNICKE DISEASE", "Coccidioidomycosis infection", "Coccidioidomycosis (disorder)", "Coccidioides immitis Infection", "coccidioidomycosis (diagnosis)", "Coccidioides immitis infection", "Coccidioidomycosis, unspecified", "Coccidioides immitis Infections", "Infection, Coccidioides immitis", "Infections, Coccidioides immitis", "Infection by Coccidioides immitis", "San Joaquin (Valley); fever (etiology)", "fever; San Joaquin (Valley) (etiology)", "Coccidioides immitis infectious disease", "Infection caused by Coccidioides immitis", "Coccidioides immitis disease or disorder", "Primary extrapulmonary coccidioidomycosis", "primary extrapulmonary coccidioidomycosis", "San Joaquin (Valley); fever (manifestation)", "fever; San Joaquin (Valley) (manifestation)", "Coccidioides immitis caused disease or disorder", "Infection caused by Coccidioides immitis (disorder)", "Primary extrapulmonary coccidioidomycosis (disorder)", "primary extrapulmonary coccidioidomycosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coccidioidomycosis", "shortest_name_length": 12}
{"curie": "MONDO:0015597", "names": ["LPP", "PPP", "acropustulosis", "Acropustulosis", "Palmoplantar pustules", "Palmoplantar Pustulosis", "Pustular acrodermatitis", "Palmoplantar pustulosis", "Psoriasis with pustules", "palmoplantar pustulosis", "Palmoplantaris Pustulosis", "pustulosis palmoplantaris", "pustulosis of palm and sole", "localized pustular psoriasis", "Localised pustular psoriasis", "Localized pustular psoriasis", "Pustulosis of palms and soles", "Pustulosis of Palms and Soles", "PPP - Palmoplantar pustulosis", "Palmoplantar pustular psoriasis", "palmoplantar pustular psoriasis", "Pustulosis Palmaris et Plantaris", "pustulosis palmaris et plantaris", "Pustulosis palmaris et plantaris", "Pustular psoriasis of palms and soles", "Pustular Psoriasis of Palms and Soles", "Chronic palmoplantar pustular psoriasis", "Localized pustular psoriasis (disorder)", "Localized pustular psoriasis (diagnosis)", "Pustular psoriasis of the palms and soles", "psoriasis; pustular, palmaris et plantaris", "pustular; psoriasis, palmaris et plantaris", "palmoplantar pustular psoriasis (diagnosis)", "Pustular psoriasis of the palms and/or soles", "pustular psoriasis of the palms and/or soles", "Pustular psoriasis of palms and soles (disorder)", "Recalcitrant pustular eruption of palms and soles"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pustulosis palmaris et plantaris", "shortest_name_length": 3}
{"curie": "UMLS:C0273058", "names": ["Traumatic intracranial bleeding", "Traumatic intracranial hemorrhage", "Traumatic Intracranial Hemorrhage", "Traumatic Intracranial Hemorrhages", "Traumatic intracranial haemorrhage", "Intracranial Hemorrhage, Traumatic", "Hemorrhage, Traumatic Intracranial", "hemorrhage; traumatic, intracranial", "traumatic; hemorrhage, intracranial", "Hemorrhages, Traumatic Intracranial", "Hemorrhage, Intracranial, Traumatic", "Intracranial Hemorrhages, Traumatic", "intracranial; hemorrhage, traumatic", "hemorrhage; intracranial, traumatic", "Traumatic intracranial hemorrhage NOS", "Traumatic intracranial haemorrhage NOS", "Intracranial hemorrhage following injury", "head injury with intracranial hemorrhage", "Intracranial haemorrhage following injury", "Intracranial hemorrhage following injury, NOS", "Intracranial haemorrhage following injury, NOS", "Intracranial hemorrhage following injury (disorder)", "head injury with intracranial hemorrhage (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Traumatic intracranial hemorrhage", "shortest_name_length": 31}
{"curie": "UMLS:C0856013", "names": ["MALT Type Extranodal Marginal Zone B-Cell Lymphoma Stage II", "Extranodal Marginal Zone B-Cell Lymphoma (MALT Type) Stage II", "Extranodal marginal zone B-cell lymphoma (MALT type) stage II", "Stage II Extranodal Marginal Zone B-Cell Lymphoma (MALT Type )", "Stage II Extranodal Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue", "Stage II Extranodal Marginal Zone B-Cell Lymphoma of Mucosa-Associated Lymphoid Tissue", "Ann Arbor Stage II Extranodal Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extranodal marginal zone B-cell lymphoma (MALT type) stage II", "shortest_name_length": 59}
{"curie": "MONDO:0007124", "names": ["AEC", "AEC syndrome", "AEC SYNDROME", "syndrome aec", "Aec syndrome", "hay well syndrome", "syndrome hay-wells", "hay-Wells syndrome", "hay-wells syndrome", "Hay-Wells syndrome", "HAY-WELLS SYNDROME", "hays wells syndrome", "Rapp-Hodgkins syndrome", "Hay Wells Syndrome Dominant Form", "Seres-Santamaria Arimany Muniz syndrome", "Hay Wells syndrome of ectodermal dysplasia", "Hay-Wells syndrome of ectodermal dysplasia", "ankyloblepharon ectodermal defects cleft lip/palate", "ankyloblepharon-ectodermal defects-cleft LIP/palate", "ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE", "Ankyloblepharon-Ectodermal Defects-Cleft Lip/Palate", "ANKYLOBLEPHARON-ECTODERMAL DEFECTS, CLEFT LIP/PALATE", "Hay-Wells syndrome of ectodermal dysplasia (disorder)", "Ankyloblepharon-ectodermal dysplasia-clefting syndrome", "Ankyloblepharon-Ectodermal Defects-Cleft Lip-Cleft Palate", "Ankyloblepharon, ectodermal defects, cleft lip and palate", "ankyloblepharon-ectodermal defects-cleft lip/palate syndrome", "Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome", "AEC - Ankyloblepharon, ectodermal defects, cleft lip and palate", "ankyloblepharon-ectodermal defects-cleft lip and palate syndrome", "Ankyloblepharon-Ectodermal Defects-Cleft Lip and Palate Syndrome", "cleft palate, ankyloblepharon, alveolar synechiae, and ectodermal defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ankyloblepharon-ectodermal defects-cleft lip/palate syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0020410", "names": ["aorto-right ventricular tunnel"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aorto-right ventricular tunnel", "shortest_name_length": 30}
{"curie": "MONDO:0018059", "names": ["Epidemic meningitis", "epidemics meningitis", "MENINGOCOCCAL MENINGITIS", "meningitis meningococcal", "Meningitis meningococcal", "Meningitis;meningococcal", "Meningococcal meningitis", "meningococcal meningitis", "meningococcic meningitis", "MENINGITIS MENINGOCOCCAL", "Meningococcal Meningitis", "Cerebrospinal meningitis", "Meningitis, Meningococcic", "Meningitis, Cerebrospinal", "Meningitis, Meningococcal", "MENINGITIS, MENINGOCOCCAL", "Neisseria meningitides meningitis", "Meningococcal cerebrospinal fever", "Meningococcal meningitis (disorder)", "meningococcal meningitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "meningococcal meningitis", "shortest_name_length": 19}
{"curie": "UMLS:C0234297", "names": ["Primary Taste Disorder", "Primary taste disorder", "Taste disorder, primary", "Taste Disorder, Primary", "Primary Taste Disorders", "Taste Disorders, Primary", "Primary taste disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Taste Disorder, Primary", "shortest_name_length": 22}
{"curie": "MONDO:0003039", "names": ["anomia", "Anomia", "ANOMIA", "Dysnomia", "dysnomia", "Dysnomias", "Anomic aphasia", "Anomic Aphasia", "anomic aphasia", "nominal aphasia", "Amnesic aphasia", "Aphasia, anomic", "Amnesic Aphasia", "Nominal aphasia", "APHASIA NOMINAL", "Nominal Aphasia", "Aphasia, Anomic", "Aphasia nominal", "Aphasia, amnesic", "Anomic dysphasia", "Aphasia, Amnesic", "Aphasia, Nominal", "Amnestic aphasia", "Anomic Dysphasia", "anomic dysphasia", "Aphasia, nominal", "amnestic aphasia", "Aphasia, amnestic", "Nominal dysphasia", "Anomic Dysphasias", "Nominal Dysphasia", "Dysphasia, Anomic", "Nominal Dysphasias", "Dysphasias, Anomic", "Dysphasia, Nominal", "Dysphasias, Nominal", "Word-finding difficulty", "anomic aphasia (finding)", "Anomic aphasia (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nominal aphasia", "shortest_name_length": 6}
{"curie": "MONDO:0005534", "names": ["Ileocolitis", "ileocolitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ileocolitis", "shortest_name_length": 11}
{"curie": "MONDO:0010447", "names": ["MRX19", "XLID19", "X-linked mental retardation 19", "MENTAL RETARDATION, X-LINKED 19", "Mental Retardation, X-Linked 19", "mental retardation, X-linked 19", "intellectual disability, X-linked 19", "mental retardation, X-linked type 19", "intellectual disability, X-linked type 19", "X-linked mental retardation 19 (MRX19, XLMR19)", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 19", "non-syndromic X-linked intellectual disability 19", "RPS6KA3 non-syndromic X-linked intellectual disability", "intellectual developmental disorder, X-linked 19, X-linked dominant", "non-syndromic X-linked intellectual disability caused by mutation in RPS6KA3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 19", "shortest_name_length": 5}
{"curie": "MONDO:0032849", "names": ["HLBKS", "NEDSOSB", "HALPERIN-BIRK SYNDROME", "Halperin-Birk syndrome", "neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies", "NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA, OPTIC ATROPHY, SEIZURES, AND STRUCTURAL BRAIN ANOMALIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies", "shortest_name_length": 5}
{"curie": "MONDO:0004913", "names": ["Alternating esotropia", "alternating esotropia", "Esotropia, alternating", "Alternating cross eyes", "Alternating esotropia, NOS", "Alternating esotropia (disorder)", "alternating esotropia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alternating esotropia", "shortest_name_length": 21}
{"curie": "MONDO:0023089", "names": ["erythroplasia", "erythroplakia", "Erythroplasia", "Erythroplakia", "Erythroplasias", "Erythroplakia, NOS", "Erythroplasia, NOS", "Erythroplakia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythroplakia", "shortest_name_length": 13}
{"curie": "UMLS:C5203852", "names": ["Prostate Large Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Large Cell Neuroendocrine Carcinoma", "shortest_name_length": 44}
{"curie": "MONDO:0024480", "names": ["eyelid; dermatosis", "dermatosis; eyelid", "dermatosis of eyelid", "Dermatosis of eyelid", "Disorder of skin of eyelid", "Dermatosis of eyelid (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermatosis of eyelid", "shortest_name_length": 18}
{"curie": "MONDO:0014676", "names": ["EDMD3", "Emery-Dreifuss Muscular Dystrophy 3", "autosomal recessive Emery-Dreifuss muscular dystrophy 3", "Emery-Dreifuss Muscular Dystrophy 3, Autosomal Recessive", "EMERY-Dreifuss muscular dystrophy 3, autosomal recessive", "EMERY-DREIFUSS MUSCULAR DYSTROPHY 3, AUTOSOMAL RECESSIVE", "Emery-Dreifuss muscular dystrophy 3, autosomal recessive", "LMNA autosomal recessive Emery-Dreifuss muscular dystrophy", "Emery-Dreifuss Muscular Dystrophy, Atypical, Autosomal Recessive", "autosomal recessive Emery-Dreifuss muscular dystrophy caused by mutation in LMNA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Emery-Dreifuss muscular dystrophy 3, autosomal recessive", "shortest_name_length": 5}
{"curie": "MONDO:0005609", "names": ["zona", "ZONA", "Zona", "zonas", "zoster", "Zoster", "shingles", "SHINGLES", "Shingles", "Zoster NOS", "herpes zona", "Herpes zoster", "HERPES ZOSTER", "Herpes Zoster", "herpes zoster", "herpes Zoster", "herpes; zoster", "zoster; herpes", "Herpes zoster NOS", "Herpes zoster, NOS", "Shingles (Disease)", "Herpes zoster disease", "Zoster [herpes zoster]", "postherpetic neuralgia", "Herpes zoster infection", "herpes zoster infection", "Herpes zoster (disorder)", "herpes zoster (diagnosis)", "Acute posterior ganglionitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "herpes zoster", "shortest_name_length": 4}
{"curie": "UMLS:C0018843", "names": ["heatstroke", "Heatstroke", "HEAT STROKE", "Heat Stroke", "heatstrokes", "Heatstrokes", "Overheating", "Heat stroke", "heat stroke", "Stroke, Heat", "THERMOPLEGIA", "Heat Strokes", "thermoplegia", "Thermoplegia", "stroke; heat", "heat strokes", "heat; stroke", "HEAT APOPLEXY", "Heat apoplexy", "apoplexy; heat", "heat; apoplexy", "Heat stroke, NOS", "heat hyperpyrexia", "Heat hyperpyrexia", "heat; hyperpyrexia", "hyperpyrexia; heat", "Heat stroke (disorder)", "heat stroke (diagnosis)", "heat apoplexy or hyperpyrexia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Heat Stroke", "shortest_name_length": 10}
{"curie": "UMLS:C0855177", "names": ["Stage II Bladder Adenocarcinoma", "Bladder adenocarcinoma stage II", "Stage II Bladder Adenocarcinoma AJCC v6", "Stage II Bladder Adenocarcinoma AJCC v7", "Stage II Bladder Adenocarcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder adenocarcinoma stage II", "shortest_name_length": 31}
{"curie": "MONDO:0013276", "names": ["REYNOLD SYNDROME", "reynold syndrome", "Reynolds syndrome", "REYNOLDS SYNDROME", "reynolds syndrome", "Reynold's syndrome", "Primary biliary cirrhosis and systemic scleroderma", "primary biliary cirrhosis and systemic scleroderma", "primary biliary cirrhosis with systemic scleroderma", "cirrhosis primary biliary with systemic scleroderma", "primary biliary cirrhosis with systemic scleroderma (diagnosis)", "Primary biliary cirrhosis co-occurrent with systemic scleroderma", "PRIMARY BILIARY CIRRHOSIS, SCLERODERMA, RAYNAUD DISEASE, AND TELANGIECTASIA", "primary biliary cirrhosis, Scleroderma, Raynaud disease, and telangiectasia", "Primary biliary cirrhosis co-occurrent with systemic scleroderma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reynolds syndrome", "shortest_name_length": 16}
{"curie": "EFO:0009363", "names": ["chronic central serous retinopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic central serous retinopathy", "shortest_name_length": 34}
{"curie": "UMLS:C0160347", "names": ["Injury to stomach with open wound into cavity", "injury of stomach with open wound into cavity", "Injury to Stomach with Open Wound into Cavity", "Injury to stomach, with open wound into cavity", "injury of stomach with open wound into cavity (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury to stomach with open wound into cavity", "shortest_name_length": 45}
{"curie": "MONDO:0018815", "names": ["ABC", "Aneurysmal bone cyst", "bone cyst aneurysmal", "Aneurysmal Bone Cyst", "aneurysmal bone cyst", "Aneurysmal Bone Cysts", "Bone Cyst, Aneurysmal", "Cyst, Aneurysmal Bone", "ANEURYSMAL BONE CYSTS", "aneurysmal bone cysts", "cyst; bone, aneurysmal", "Bone Cysts, Aneurysmal", "Cysts, Aneurysmal Bone", "aneurysmal cyst of bone", "aneurysmal cyst in bone", "Aneurysmal Cyst of Bone", "ABC - Aneurysmal bone cyst", "Aneurysmal Cyst of the Bone", "aneurysmal cyst of the bone", "aneurysmal bone cyst (disease)", "Aneurysmal bone cyst (disorder)", "aneurysmal bone cyst (diagnosis)", "aneurysmal cyst in bone (diagnosis)", "Aneurysmal bone cyst, unspecified site", "Aneurysmal bone cyst, site unspecified", "Aneurysmal bone cyst (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aneurysmal bone cyst", "shortest_name_length": 3}
{"curie": "MONDO:0005945", "names": ["Scleroma", "scleroma", "scleroma nasi", "rhinoscleroma", "RHINOSCLEROMA", "Rhinoscleroma", "Scleroma, Nasal", "Rhinoscleroma (disorder)", "rhinoscleroma (diagnosis)", "Infection by Klebsiella rhinoscleromatis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rhinoscleroma", "shortest_name_length": 8}
{"curie": "UMLS:C0011361", "names": ["Dental fistula", "Dental Fistula", "Dental Fistulas", "Fistula, Dental", "Gingival Fistula", "Fistulas, Dental", "GINGIVAL FISTULA", "Fistula, Gingival", "Gingival Fistulas", "Fistulas, Gingival", "Alveolar process fistula", "Fistula, alveolar process", "Periapical abscess with sinus", "Periapical Abscess with Sinus", "periapical abscess with sinus", "Periapical abscess with a sinus", "Periapical abscess with sinus tract", "dentoalveolar abscess with sinus tract", "periapical abscess with sinus (diagnosis)", "Periapical abscess with sinus tract (disorder)", "dentoalveolar abscess with sinus tract (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dental Fistula", "shortest_name_length": 14}
{"curie": "UMLS:C0241742", "names": ["bloody wound", "Wound bleeding", "wound bleeding", "WOUND BLEEDING", "bleeding wound", "bleeding wounds", "Wound hemorrhage", "hemorrhage wound", "hemorrhage wounds", "Wound haemorrhage", "Wound hemorrhage (finding)", "bloody wound (physical finding)", "bleeding wound (physical finding)", "Wound hemorrhage (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wound hemorrhage", "shortest_name_length": 12}
{"curie": "UMLS:C1519719", "names": ["Type I Endometrial Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Type I Endometrial Adenocarcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C3665418", "names": ["labile htn", "Labile hypertension", "HYPERTENSION LABILE", "labile hypertension", "Hypertension;labile", "LABILE HYPERTENSION", "White coat hypertension", "labile hypertension (diagnosis)", "labile hypertension was observed", "labile hypertension (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Labile hypertension", "shortest_name_length": 10}
{"curie": "UMLS:C0280392", "names": ["Relapsed Hypopharyngeal Epidermoid Carcinoma", "Relapsed Epidermoid Carcinoma of Hypopharynx", "Recurrent Epidermoid Carcinoma of Hypopharynx", "Recurrent Hypopharyngeal Epidermoid Carcinoma", "hypopharynx squamous cell carcinoma, recurrent", "Relapsed Hypopharyngeal Squamous Cell Carcinoma", "Relapsed Squamous Cell Carcinoma of Hypopharynx", "Relapsed Epidermoid Carcinoma of the Hypopharynx", "Recurrent Squamous Cell Carcinoma of Hypopharynx", "Hypopharyngeal squamous cell carcinoma recurrent", "Recurrent Hypopharyngeal Squamous Cell Carcinoma", "Recurrent Epidermoid Carcinoma of the Hypopharynx", "hypopharyngeal squamous cell carcinoma, recurrent", "epidermoid carcinoma of the hypopharynx, recurrent", "Relapsed Squamous Cell Carcinoma of the Hypopharynx", "Recurrent Hypopharyngeal Throat Squamous Cell Cancer", "recurrent squamous cell carcinoma of the hypopharynx", "Squamous cell carcinoma of the hypopharynx recurrent", "Recurrent Squamous Cell Carcinoma of the Hypopharynx", "squamous cell carcinoma of the hypopharynx, recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypopharyngeal squamous cell carcinoma recurrent", "shortest_name_length": 44}
{"curie": "MONDO:0013213", "names": ["CIHL", "hearing loss, cisplatin-induced, susceptibility to", "HEARING LOSS, CISPLATIN-INDUCED, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, cisplatin-induced, susceptibility to", "shortest_name_length": 4}
{"curie": "MONDO:0019004", "names": ["WT1", "Wilms", "nephroma", "Nephroma", "nephromas", "wilm tumor", "Wilm Tumor", "tumor wilms", "Wilms Tumor", "Wilms tumor", "wilms tumor", "WILMS TUMOR", "Wilms' tumor", "Wilm's Tumor", "tumor wilm's", "tumors wilms", "tumor wilms'", "wilm's tumor", "wilms' tumor", "Wilm's tumor", "Wilms; tumor", "wilms tumour", "Wilms tumour", "tumor; Wilms", "Wilms' Tumor", "Tumor, Wilms", "Wilms Tumor 1", "tumor wilms's", "Nephroma, NOS", "Tumor, Wilms'", "wilms' tumour", "Wilms' tumour", "WILMS TUMOR 1", "Wilm's tumour", "tumor, Wilms'", "tumors wilm's", "nephroblastoma", "Nephroblastoma", "NEPHROBLASTOMA", "Nephroblastomas", "kidney; embryoma", "KIDNEY, EMBRYOMA", "embryoma; kidney", "Renal Wilms Tumor", "renal Wilms tumor", "kidney Wilms tumor", "Embryonal nephroma", "Renal Wilms' Tumor", "Embryonal Nephroma", "Renal adenosarcoma", "embryonal nephroma", "renal Wilms' tumor", "Kidney Wilms Tumor", "Nephroblastoma NOS", "renal Wilms' tumour", "Nephroblastoma, NOS", "RENAL CANCER, WILMS", "adult nephroblastoma", "renal embryonic tumor", "Kidney Nephroblastoma", "Renal embryonic tumor", "[M]Nephroblastoma NOS", "Embryonal adenosarcoma", "nephroblastoma of kidney", "NEPHROBLASTOMA, MALIGNANT", "nephroblastoma, malignant", "Nephroblastoma (disorder)", "Wilms tumor of the kidney", "Wilms Tumor of the Kidney", "Wilms' Tumor of the Kidney", "Wilms' tumor of the kidney", "childhood renal Wilms tumor", "Wilms tumor (nephroblastoma)", "Nephroblastoma (Wilms tumor)", "KIDNEY, EMBRYONAL MIXED TUMOR", "childhood renal Wilms' cancer", "nonanaplastic renal wilms tumor", "Nonanaplastic renal Wilm's tumor", "nonanaplastic renal Wilm's tumor", "KIDNEY, CARCINOSARCOMA, EMBRYONAL", "Nonanaplastic renal Wilm's tumour", "KIDNEY, ADENOMYOSARCOMA, EMBRYONAL", "nephroblastoma of kidney (diagnosis)", "Nephroblastoma (morphologic abnormality)", "Wilms tumor and other childhood kidney tumors", "Wilms' tumor and other childhood kidney tumors"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kidney Wilms tumor", "shortest_name_length": 3}
{"curie": "MONDO:0001198", "names": ["Acquired thrombocytopenia", "acquired thrombocytopenia", "secondary thrombocytopenia", "Secondary thrombocytopenia", "secondary; thrombocytopenia", "thrombocytopenia; secondary", "Thrombocytopenia, secondary", "Thrombocytopenia: secondary NOS", "Acquired thrombocytopenia (disorder)", "Secondary thrombocytopenia (disorder)", "secondary thrombocytopenia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired thrombocytopenia", "shortest_name_length": 25}
{"curie": "MONDO:0018757", "names": ["supratip dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "supratip dysplasia", "shortest_name_length": 18}
{"curie": "MONDO:0011051", "names": ["Short limb dwarfism Al Gazali type", "Lethal neonatal short limb dwarfism", "lethal neonatal short limb dwarfism", "lethal short limb skeletal dysplasia Al Gazali type", "lethal short-limb skeletal dysplasia, Al Gazali type", "Lethal short-limb skeletal dysplasia, Al Gazali type", "LETHAL SHORT-LIMB SKELETAL DYSPLASIA, AL GAZALI TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal short-limb skeletal dysplasia, Al Gazali type", "shortest_name_length": 34}
{"curie": "MONDO:0012728", "names": ["BRGDA2", "Brugada Syndrome 2", "Brugada syndrome 2", "BRUGADA SYNDROME 2", "GPD1L Brugada syndrome", "Brugada syndrome type 2", "Brugada syndrome 2 (diagnosis)", "Brugada syndrome caused by mutation in GPD1L"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brugada syndrome 2", "shortest_name_length": 6}
{"curie": "UMLS:C0002899", "names": ["glutathione metabolism anemias", "anemia; glutathione metabolism", "anemia; glutathione metabolic disorder", "anemia; disorder glutathione metabolism", "glutathione metabolism anemias (diagnosis)", "metabolic disorder; glutathione with anemia", "disorder; glutathione metabolism with anemia", "Anemia due to Disorder of Glutathione Metabolism", "Anemias due to disorders of glutathione metabolism", "Anaemias due to disorders of glutathione metabolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anaemias due to disorders of glutathione metabolism", "shortest_name_length": 30}
{"curie": "UMLS:C0520758", "names": ["Prolonged neuromuscular block", "Neuromuscular block prolonged", "Prolonged neuromuscular block (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prolonged neuromuscular block", "shortest_name_length": 29}
{"curie": "UMLS:C0520793", "names": ["gastroenteritis cryptococcal", "Cryptococcal Gastroenteritis", "Cryptococcal gastroenteritis", "Gastroenteritis cryptococcal", "Cryptococcal gastroenteritis (disorder)", "Cryptococcal gastroenteritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cryptococcal gastroenteritis", "shortest_name_length": 28}
{"curie": "MONDO:0005148", "names": ["MOD", "T2D", "MODY", "aodm", "AODM", "niddm", "MVCD5", "NIDDM", "NCDMM", "diabetes", "diabete type 2", "type 2 diabetes", "Type 2 diabetes", "Diabetes Type 2", "Diabetes;Type 2", "Type 2 Diabetes", "NIDDM; diabetes", "diabetes; NIDDM", "diabetes type 2", "Type II Diabetes", "type II diabetes", "Diabetes, Type 2", "Type II diabetes", "diabetes, type 2", "diabetes type ii", "diabetes, type ii", "type II; diabetes", "diabetes; type II", "Diabetes, Type II", "insulin resistance", "late onset diabetes", "adult-onset diabetes", "nonketotic; diabetes", "diabetes; nonketotic", "adult onset diabetes", "Adult-Onset Diabetes", "Diabetes;adult onset", "Adult Onset Diabetes", "adult-onset; diabetes", "DIABETES, ADULT ONSET", "diabetes; adult-onset", "maturity onset diabetes", "Maturity onset diabetes", "Maturity-Onset Diabetes", "maturity-onset diabetes", "NIDDM diabetes mellitus", "Maturity Onset Diabetes", "MATURITY-ONSET DIABETES", "DIABETES, MATURITY ONSET", "Type 2 diabetes mellitus", "diabetes mellitis type 2", "Stable Diabetes Mellitus", "TYPE 2 DIABETES MELLITUS", "type 2 diabetes mellitus", "Type 2 Diabetes Mellitus", "Diabetes mellitus type 2", "diabetes mellitus type 2", "Diabetes, Maturity-Onset", "maturity-onset; diabetes", "diabetes; maturity-onset", "Diabetes Mellitus, Stable", "Diabetes mellitus, Type 2", "type II diabetes mellitus", "Diabetes mellitus type II", "Diabetes mellitus (NIDDM)", "diabetes mellitus, type 2", "diabetes mellitus type ii", "Diabetes Mellitus, Type 2", "Type II diabetes mellitus", "Diabetes mellitus, type 2", "diabetes mellitis type II", "type ii diabetes mellitus", "Type II Diabetes Mellitus", "DIABETES MELLITUS, TYPE 2", "Diabetes mellitus Type II", "ketosis resistant diabetes", "DIABETES MELLITUS, TYPE II", "Diabetes Mellitus, Type II", "Diabetes mellitus, type II", "diabetes mellitus, type II", "DIABETES, KETOSIS RESISTANT", "Diabetes;non insulin depend", "Slow-Onset Diabetes Mellitus", "Diabetes Mellitus, Slow-Onset", "Adult-Onset Diabetes Mellitus", "Noninsulin-dependent diabetes", "Diabetes Mellitus, Slow Onset", "Noninsulin Dependent Diabetes", "noninsulin dependent diabetes", "adult onset diabetes mellitus", "ADULT ONSET DIABETES MELLITUS", "Non-insulin-dependent diabetes", "Diabetes Mellitus, Adult Onset", "Diabetes non-insulin dependent", "non-insulin dependent diabetes", "non insulin dependent diabetes", "Diabetes Mellitus, Adult-Onset", "Non-insulin dependent diabetes", "Non-Insulin Dependent Diabetes", "Diabetes mellitus - adult onset", "T2DM - diabetes mellitus type 2", "non-insulin-dependent; diabetes", "DIABETES MELLITUS (ADULT ONSET)", "T2DM - Type 2 Diabetes mellitus", "diabetes; non-insulin-dependent", "T2DM - type 2 diabetes mellitus", "Maturity Onset Diabetes Mellitus", "DIABETES MELLITUS NOS LATE ONSET", "Maturity onset diabetes mellitus", "Diabetes mellitus maturity onset", "Maturity-Onset Diabetes Mellitus", "DIABETES MELLITUS NON INSULIN-DEP", "insulin resistance susceptibility", "Diabetes Mellitus, Maturity-Onset", "Diabetes Mellitus, Maturity Onset", "obsolete_type II diabetes mellitus", "PON1 ENZYME ACTIVITY, VARIATION IN", "Ketosis-Resistant Diabetes Mellitus", "Diabetes mellitus, adult onset type", "Diabetes mellitus type 2 (disorder)", "insulin resistance, severe, digenic", "Diabetes Mellitus, Ketosis Resistant", "Type 2 diabetes mellitus (diagnosis)", "Diabetes Mellitus, Ketosis-Resistant", "INSULIN RESISTANCE, SUSCEPTIBILITY TO", "insulin resistance, susceptibility to", "Noninsulin-dependent diabetes mellitus", "Noninsulin dependent diabetes mellitus", "noninsulin dependent diabetes mellitus", "Noninsulin Dependent Diabetes Mellitus", "NONINSULIN-DEPENDENT DIABETES MELLITUS", "Noninsulin-Dependent Diabetes Mellitus", "noninsulin-dependent diabetes mellitus", "DIABETES MELLITUS NON INSULIN DEPENDENT", "diabetes mellitus, noninsulin-dependent", "Diabetes mellitus non-insulin-dependent", "non-insulin-dependent diabetes mellitus", "Diabetes Mellitus, Noninsulin Dependent", "non-insulin dependent diabetes mellitus", "Diabetes Mellitus, Noninsulin-Dependent", "DIABETES MELLITUS, NONINSULIN-DEPENDENT", "Non-Insulin-Dependent Diabetes Mellitus", "Non-insulin dependent diabetes mellitus", "Diabetes mellitus, noninsulin-dependent", "Non-insulin-dependent diabetes mellitus", "Non-Insulin Dependent Diabetes Mellitus", "DIABETES MELLITUS, NON-INSULIN DEPENDENT", "Diabetes Mellitus, Non Insulin Dependent", "Diabetes Mellitus, Non-Insulin-Dependent", "RETINOPATHY, DIABETIC, SUSCEPTIBILITY TO", "CORONARY ARTERY DISEASE, SUSCEPTIBILITY TO", "diabetes mellitus, noninsulin-dependent, 2", "CORONARY ARTERY SPASM 2, SUSCEPTIBILITY TO", "type 2 diabetes mellitus, susceptibility to", "ORGANOPHOSPHATE POISONING, SUSCEPTIBILITY TO", "diabetes mellitus, type 2, susceptibility to", "TYPE 2 DIABETES MELLITUS, PROTECTION AGAINST", "DIABETES MELLITUS, TYPE 2, PROTECTION AGAINST", "diabetes mellitus, type II, susceptibility to", "diabetes mellitus, type 2, protection against", "insulin resistance susceptibility (diagnosis)", "Type 2 Diabetes Mellitus Non-Insulin Dependent", "type 2 diabetes mellitus non-insulin dependent", "NIDDM - Non-insulin dependent diabetes mellitus", "diabetes mellitus, noninsulin-dependent, late onset", "diabetes mellitus, noninsulin-dependent, association with", "diabetes mellitus, noninsulin-dependent, susceptibility to", "diabetes mellitus, non-insulin-dependent, susceptibility to", "hypertension, insulin resistance-related, susceptibility to", "MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 5", "MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 5 (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type 2 diabetes mellitus", "shortest_name_length": 3}
{"curie": "UMLS:C1512256", "names": ["FIGO Grade 3 Endometrial Mucinous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Grade 3 Endometrial Mucinous Adenocarcinoma", "shortest_name_length": 48}
{"curie": "UMLS:C0280307", "names": ["Buccal Mucosa Verrucous Carcinoma", "Verrucous Carcinoma of Buccal Mucosa", "Verrucous Carcinoma of the Buccal Mucosa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Buccal Mucosa Verrucous Carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0044788", "names": ["perihilar ICC", "perihilar cholangiocarcinoma", "perihilar bile duct carcinoma", "perihilar intrahepatic cholangiocarcinoma", "Large Duct Intrahepatic Cholangiocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "perihilar intrahepatic cholangiocarcinoma", "shortest_name_length": 13}
{"curie": "UMLS:C4684865", "names": ["CALD", "Cerebral Adrenoleukodystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebral Adrenoleukodystrophy", "shortest_name_length": 4}
{"curie": "UMLS:C1332043", "names": ["AIDS-Related Enterocolitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Enterocolitis", "shortest_name_length": 26}
{"curie": "UMLS:C4763751", "names": ["Transformed Chronic Lymphocytic Leukemia to Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transformed Chronic Lymphocytic Leukemia to Diffuse Large B-Cell Lymphoma", "shortest_name_length": 73}
{"curie": "MONDO:0004973", "names": ["Adenosquamous Lung Cancer", "LUNG CANCER ADENOSQUAMOUS", "adenosquamous lung cancer", "adenosquamous lung carcinoma", "Adenosquamous Lung Carcinoma", "Lung Adenosquamous Carcinoma", "lung adenosquamous carcinoma", "Adenosquamous cell lung cancer", "adenosquamous cell lung cancer", "lung cancer, adenosquamous cell", "adenosquamous carcinoma of lung", "Adenosquamous carcinoma of lung", "adenosquamous cell lung carcinoma", "Adenosquamous Cell Lung Carcinoma", "Adenosquamous cell lung cancer NOS", "Primary adenosquamous carcinoma of lung", "primary adenosquamous carcinoma of lung", "Adenosquamous carcinoma of lung (disorder)", "adenosquamous carcinoma of lung (diagnosis)", "non-oat cell lung cancer, adenosquamous cell", "lung malignant carcinoma adenosquamous primary", "Primary adenosquamous carcinoma of lung (disorder)", "epidermoid and adenocarcinoma of the lung, combined", "primary adenosquamous carcinoma of lung (diagnosis)", "adenocarcinoma and epidermoid of the lung, combined", "adenocarcinoma and squamous cell of the lung, combined", "squamous cell and adenocarcinoma of the lung, combined"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenosquamous lung carcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0011129", "names": ["GLC1C", "glaucoma type 1C", "GLAUCOMA 1, OPEN ANGLE, C", "Glaucoma 1, Open Angle, C", "glaucoma 1C, primary open angle", "GLAUCOMA 1, PRIMARY OPEN ANGLE, C", "glaucoma 1, primary open angle, C"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glaucoma type 1C", "shortest_name_length": 5}
{"curie": "MONDO:0014113", "names": ["CFC3", "CARDIOFACIOCUTANEOUS SYNDROME 3", "cardiofaciocutaneous syndrome 3", "MAP2K1 cardiofaciocutaneous syndrome", "cardiofaciocutaneous syndrome type 3", "cardiofaciocutaneous syndrome caused by mutation in MAP2K1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiofaciocutaneous syndrome 3", "shortest_name_length": 4}
{"curie": "UMLS:C1334747", "names": ["Methotrexate-Associated Follicular Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Methotrexate-Associated Follicular Lymphoma", "shortest_name_length": 43}
{"curie": "MONDO:0013168", "names": ["CMD1DD", "dilated cardiomyopathy 1DD", "Dilated Cardiomyopathy-1DD", "cardiomyopathy, dilated, 1DD", "Cardiomyopathy, Dilated, 1DD", "CARDIOMYOPATHY, DILATED, 1DD", "dilated cardiomyopathy type 1DD", "cardiomyopathy, dilated, type 1Dd", "RBM20 familial isolated dilated cardiomyopathy", "familial isolated dilated cardiomyopathy caused by mutation in RBM20"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1DD", "shortest_name_length": 6}
{"curie": "UMLS:C1335919", "names": ["Sarcoma by AJCC Grade", "AJCC Tumor Grade in Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sarcoma by AJCC Grade", "shortest_name_length": 21}
{"curie": "MONDO:0005499", "names": ["brain glioma", "lower grade glioma", "glial tumor of brain", "Glial tumor of brain", "Glial tumour of brain", "brain malignant glioma", "malignant glioma of brain", "Glial tumor of brain (disorder)", "glial tumor of brain (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brain glioma", "shortest_name_length": 12}
{"curie": "UMLS:C4721700", "names": ["Stage IV Laryngeal Cancer", "Stage IV Laryngeal Throat Cancer", "Stage IV Laryngeal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Laryngeal Cancer AJCC v7", "shortest_name_length": 25}
{"curie": "UMLS:C0947885", "names": ["Congenital Dental Disorder", "Dental disorders congenital"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dental disorders congenital", "shortest_name_length": 26}
{"curie": "MONDO:0024666", "names": ["Benign Epithelial Skin Tumor", "benign epithelial skin tumor", "Benign Skin Epithelium Tumor", "benign skin epithelium tumor", "benign skin epithelium neoplasm", "Benign Skin Epithelium Neoplasm", "benign epithelial skin neoplasm", "Benign Epithelial Skin Neoplasm", "epithelial skin neoplasm, benign", "Benign epithelial neoplasm of skin", "Benign tumor of surface epithelium", "Benign tumour of surface epithelium", "Benign epithelial neoplasm of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign epithelial skin neoplasm", "shortest_name_length": 28}
{"curie": "MONDO:0018885", "names": ["Orbital leiomyoma", "orbital leiomyoma", "Leiomyoma of orbit", "Leiomyoma of orbit (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orbital leiomyoma", "shortest_name_length": 17}
{"curie": "MONDO:0009168", "names": ["EPV", "PVHH", "Fowler syndrome", "Fowler vasculopaty", "Fowler vasculopathy", "HYDRANENCEPHALY, FOWLER TYPE", "hydranencephaly, fowler type", "hydranencephaly, Fowler type", "Hydranencephaly, Fowler Type", "Encephaloclastic Proliferative Vasculopathy", "encephaloclastic proliferative vasculopathy", "ENCEPHALOCLASTIC PROLIFERATIVE VASCULOPATHY", "Encephaloclastic proliferative vasculopathy", "Cerebral proliferative glomeruloid vasculopathy", "cerebral proliferative glomeruloid vasculopathy", "Hydrocephaly-Hydranencephaly due to Cerebral Vasculopathy", "Hydrocephaly/hydranencephaly due to cerebral vasculopathy", "hydrocephaly/hydranencephaly due to cerebral vasculopathy", "HYDROCEPHALY/HYDRANENCEPHALY DUE TO CEREBRAL VASCULOPATHY", "proliferative vasculopathy and hydranencephaly/hydrocephaly", "Proliferative vasculopathy and hydranencephaly/hydrocephaly", "proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome", "PROLIFERATIVE VASCULOPATHY AND HYDRANENCEPHALY-HYDROCEPHALY SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fowler syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C4683411", "names": ["Thyroid Gland Papillary Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Papillary Carcinoma by AJCC v7 Stage", "shortest_name_length": 50}
{"curie": "MONDO:0018889", "names": ["hyaline body myopathy", "myosin storage myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyaline body myopathy", "shortest_name_length": 21}
{"curie": "UMLS:C0278822", "names": ["stage A bladder cancer", "stage I bladder cancer", "Stage I Bladder Cancer", "Bladder Cancer Stage I", "bladder cancer, stage I", "bladder cancer, stage A", "Stage I Bladder Carcinoma", "Stage I Carcinoma of Bladder", "stage I cancer of the bladder", "stage A cancer of the bladder", "Stage I Bladder Cancer AJCC v6", "Stage I Bladder Cancer AJCC v7", "cancer of the bladder, stage A", "cancer of the bladder, stage I", "Stage I Carcinoma of the Bladder", "stage I carcinoma of the bladder", "stage A carcinoma of the bladder", "Stage I Urinary Bladder Carcinoma", "carcinoma of the bladder, stage A", "carcinoma of the bladder, stage I", "Stage I Bladder Carcinoma AJCC v7", "Stage I Bladder Carcinoma AJCC v6", "Stage I Carcinoma of Urinary Bladder", "Stage I Bladder Cancer AJCC v6 and v7", "Jewett-Marshall Stage A Bladder Cancer", "Stage I Carcinoma of the Urinary Bladder", "Jewett-Marshall Stage A Bladder Carcinoma", "Jewett-Marshall Stage A Urinary Bladder Cancer", "Jewett-Marshall Stage A Urinary Bladder Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Carcinoma of Bladder", "shortest_name_length": 22}
{"curie": "UMLS:C0854284", "names": ["Iris Vascular Disorder", "Iris vascular disorder", "vascular; disorder iris", "vascular disorder of iris", "Iris vascular disorder NOS", "vascular disorder of iris (diagnosis)", "disease (or disorder); vascular, iris"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Iris vascular disorder", "shortest_name_length": 22}
{"curie": "MONDO:0003910", "names": ["mixed cell uveal melanoma", "Mixed Cell Uveal Melanoma", "Uveal Mixed Cell Melanoma", "mixed cell type intraocular melanoma", "melanoma, mixed cell type intraocular", "intraocular melanoma, mixed cell type", "melanoma, intraocular, mixed cell type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed cell uveal melanoma", "shortest_name_length": 25}
{"curie": "MONDO:0005769", "names": ["Hunt neuralgia", "Hunt's neuralgia", "Geniculate otalgia", "ramsey hunt syndrome", "Ramsay-Hunt syndrome", "ramsey-hunt syndrome", "Ramsay Hunt Syndrome", "Ramsay Hunt syndrome", "geniculate neuralgia", "Herpes zoster oticus", "Geniculate neuralgia", "RAMSEY HUNT SYNDROME", "herpes zoster oticus", "Geniculate Neuralgia", "Herpes Zoster Oticus", "Ramsey Hunt syndrome", "hunt ramsey syndrome", "Neuralgia, Geniculate", "hunts ramsey syndrome", "Syndrome, Ramsay Hunt", "Geniculate Neuralgias", "Ramsay Hunt syndrome 1", "Ramsay Hunt syndrome 2", "Neuralgias, Geniculate", "Neuralgia facialis vera", "neuralgia; facialis vera", "geniculate herpes zoster", "Herpes zoster cephalicus", "Geniculate Herpes Zoster", "Herpes Zoster Cephalicus", "facialis vera; neuralgia", "Hunt syndrome (formerly)", "Geniculate herpes zoster", "Herpes Zoster, Geniculate", "herpes zoster auricularis", "Herpes zoster auricularis", "Herpes Zoster Auricularis", "Hunt's syndrome (formerly)", "HZO - Herpes zoster oticus", "Ramsay Hunt's syndrome (1)", "Ramsay Hunt syndrome type 2", "Herpes zoster otitis externa", "Nervus intermedius neuralgia", "nervus intermedius neuralgia", "Ramsay Hunt syndrome type II", "facial nerve palsy due to VZV", "Facial nerve palsy due to VZV", "Ramsay Hunt Auricular Syndrome", "Herpetic Geniculate Ganglionitis", "herpetic geniculate ganglionitis", "Herpetic geniculate ganglionitis", "Ramsay Hunt syndrome - auricular", "herpes zoster with otitis externa", "facial nerve paralysis due to VZV", "Auricular Syndrome of Ramsay Hunt", "Geniculate Ganglionitis, Herpetic", "Ganglionitis, Herpetic Geniculate", "Facial nerve paralysis due to VZV", "geniculate herpes zoster infection", "Herpetic Geniculate Ganglionitides", "Geniculate herpes zoster infection", "Otitis externa due to Herpes zoster", "Geniculate Ganglionitides, Herpetic", "Otitis externa due to herpes zoster", "Herpes zoster auricularis (disorder)", "Postherpetic geniculate ganglionitis", "postherpetic geniculate ganglionitis", "herpes zoster auricularis (diagnosis)", "Ramsay Hunt syndrome type 2 (formerly)", "Otitis externa caused by Herpes zoster", "Nervus intermedius neuralgia (disorder)", "nervus intermedius neuralgia (diagnosis)", "Ramsay-Hunt syndrome (geniculate herpes)", "otitis; externa, herpes zoster (etiology)", "herpes; otitis externa, h.zoster (etiology)", "herpes zoster with otitis externa (diagnosis)", "otitis; externa, herpes zoster (manifestation)", "postherpetic geniculate ganglionitis (diagnosis)", "Otitis externa caused by Herpes zoster (disorder)", "Facial nerve palsy due to herpes zoster infection", "facial nerve palsy due to herpes zoster infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "geniculate herpes zoster", "shortest_name_length": 14}
{"curie": "MONDO:0013050", "names": ["GDFD", "lethal polymalformative syndrome, Boissel type", "growth retardation, developmental delay, facial dysmorphism", "GROWTH RETARDATION, DEVELOPMENTAL DELAY, AND FACIAL DYSMORPHISM", "growth retardation, developmental delay, and facial dysmorphism", "Growth Retardation, Developmental Delay, Coarse Facies, And Early Death"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal polymalformative syndrome, Boissel type", "shortest_name_length": 4}
{"curie": "UMLS:C2200133", "names": ["Lung Follicular Lymphoma", "follicular lymphoma of lung", "Primary Lung Follicular Lymphoma", "follicular lymphoma of lung (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "follicular lymphoma of lung", "shortest_name_length": 24}
{"curie": "UMLS:C5420434", "names": ["Maxillofacial Chondroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Maxillofacial Chondroma", "shortest_name_length": 23}
{"curie": "MONDO:0100231", "names": ["PSORAS1", "psoriatic arthritis, susceptibility to", "psoriatic arthritis, susceptibility to, 1", "psoriatic arthritis susceptibility caused by LTA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "psoriatic arthritis, susceptibility to, 1", "shortest_name_length": 7}
{"curie": "MONDO:0037744", "names": ["retromolar area neoplasm", "Tumor of retromolar area", "tumor of retromolar area", "Tumour of retromolar area", "neoplasm of retromolar area", "Neoplasm of retromolar area", "Neoplasm of retromolar area (disorder)", "neoplasm of retromolar area (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplasm of retromolar area", "shortest_name_length": 24}
{"curie": "MONDO:0009130", "names": ["DMC", "DMC disease", "DMC syndrome", "pseudo-Morquio disease type I", "DYGGVE-MELCHIOR-CLAUSEN DISEASE", "Dyggve-Melchior-Clausen disease", "Dyggve-Melchior-Clausen Disease", "Dyggve-Melchior-Clausen syndrome", "Dyggve-Melchior-Clausen Syndrome", "Dyggve-Melchior-Clausen dysplasia", "Dyggve-Melchior-Clausen syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dyggve-Melchior-Clausen disease", "shortest_name_length": 3}
{"curie": "MONDO:0100378", "names": ["AML, t(10;11)(p11.2;q23)", "acute myeloid leukemia, t(10;11)(p11.2;q23)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, t(10;11)(p11.2;q23)", "shortest_name_length": 24}
{"curie": "UMLS:C0854754", "names": ["Lip and/or oral cavity cancer", "Lip and/or oral cavity cancer NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lip and/or oral cavity cancer", "shortest_name_length": 29}
{"curie": "UMLS:C0854868", "names": ["Transformed Lymphoma", "Recurrent Transformed Non-Hodgkin Lymphoma", "Transformed Recurrent Non-Hodgkin Lymphoma", "NonHodgkin's Lymphoma Transformed Recurrent", "Non-Hodgkin's lymphoma transformed recurrent", "Transformed Recurrent Non-Hodgkin's Lymphoma", "Non-Hodgkin's Lymphoma Transformed Recurrent", "Non-Hodgkin's lymphomas transformed recurrent", "Non-Hodgkin's lymphoma transformed recurrent NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Hodgkin's lymphoma transformed recurrent", "shortest_name_length": 20}
{"curie": "MONDO:0015838", "names": ["Cordate uterus", "uterus arcuatus", "Uterus, cordate", "cordiform uterus", "Cordiform uterus", "uterus cordiformis", "Uterus cordiformis", "Uterus cordiformis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cordiform uterus", "shortest_name_length": 14}
{"curie": "MONDO:0006790", "names": ["cementosis", "Cementosis", "hypercementosis", "Hypercementosis", "Hypercementoses", "Cementum overgrowth", "Cementum hypertrophy", "Cementum hyperplasia", "Drumstick-shaped root", "Cementum overdeveloped", "Cementation hyperplasia", "cementation hyperplasia", "Hypercementosis (disorder)", "hypercementosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypercementosis", "shortest_name_length": 10}
{"curie": "UMLS:C0015704", "names": ["Nodular Elastoses", "Nodular Elastosis", "Nodular elastosis", "Elastoses, Nodular", "Elastosis, Nodular", "Nodular elastoidosis", "Nodular Elastoidoses", "Nodular Elastoidosis", "Elastoidoses, Nodular", "Elastoidosis, Nodular", "Favre-Racouchot syndrome", "Actinic comedonal plaque", "Favre Racouchot Syndrome", "Favre-Racouchot Syndrome", "Syndrome, Favre-Racouchot", "Nodular elastosis of Favre-Racouchot", "Dyselastosis with cysts and comedones", "Nodular elastosis with cysts and comedones", "Solar elastosis with comedones and follicular cysts", "Nodular elastosis with cysts and comedones (disorder)", "Nodular elastosis with cysts and comedones of Favre and Racouchot", "Nodular elastosis with cysts AND comedones of Favre and Racouchot"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Favre-Racouchot Syndrome", "shortest_name_length": 17}
{"curie": "MONDO:0011152", "names": ["PHGDHD", "PHGDH DEFICIENCY", "PHGDH Deficiency", "PHGDH deficiency", "PHOSPHOGLYCERATE DEHYDROGENASE DEFICIENCY", "PHOSPHOGLYCERATE dehydrogenase deficiency", "Phosphoglycerate Dehydrogenase Deficiency", "3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PHGDH deficiency", "shortest_name_length": 6}
{"curie": "MONDO:0010720", "names": ["pais", "PAIS", "Reifenstein", "Lubs syndrome", "lubs syndrome", "Lubs' syndrome", "Rosewater syndrome", "reifenstein syndrome", "Reifenstein syndrome", "Reifenstein Syndrome", "Rosewater's syndrome", "REIFENSTEIN SYNDROME", "Reifensteins Syndrome", "reifenstein's syndrome", "Reifenstein's syndrome", "Reifenstein's Syndrome", "gilbert dreyfus syndrome", "Gilbert-Dreyfuss syndrome", "Gilbert-Dreyfus' syndrome", "Reifenstein syndrome, partial", "partial androgen insensitivity", "Partial androgen insensitivity", "Partial Androgen Insensitivity", "ANDROGEN INSENSITIVITY, PARTIAL", "Insensitivity, Partial Androgen", "Androgen Insensitivity, Partial", "androgen insensitivity, partial", "Partial Androgen Insensitivities", "Insensitivities, Partial Androgen", "Androgen Insensitivities, Partial", "partial androgen resistance syndrome", "Partial androgen resistance syndrome", "incomplete male pseudohermaphroditism", "androgen resistance syndrome, partial", "Partial Androgen-Insensitivity Syndrome", "Partial Androgen Insensitivity Syndrome", "partial androgen insensitivity syndrome", "Partial androgen insensitivity syndrome", "androgen insensitivity syndrome, partial", "Partial Androgen-Insensitivity Syndromes", "Androgen Insensitivity Syndrome, Partial", "Androgen-Insensitivity Syndrome, Partial", "Hereditary familial hypogonadism syndrome", "Androgen-Insensitivity Syndromes, Partial", "partial androgen insensitivity (diagnosis)", "Pseudohermaphroditism, Incomplete Male, Type I", "PAIS - partial androgen insensitivity syndrome", "pseudohermaphroditism, incomplete male, type I", "Partial androgen insensitivity syndrome (disorder)", "Type I familial incomplete male pseudohermaphroditism", "type I familial incomplete male pseudohermaphroditism", "Familial incomplete male pseudohermaphroditism type 1", "Familial incomplete male pseudohermaphroditism, type 1", "FAMILIAL INCOMPLETE MALE PSEUDOHERMAPHRODITISM, TYPE 1", "familial incomplete Male pseudohermaphroditism, type 1", "androgen insensitivity, partial, with or without breast cancer", "ANDROGEN INSENSITIVITY, PARTIAL, WITH OR WITHOUT BREAST CANCER", "androgen insensitivity, partial, with or without breast cancer, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial androgen insensitivity syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0040676", "names": ["great vessel cancer", "Great Vessel Cancer", "Malignant Great Vessel Tumor", "great vessel of heart cancer", "malignant great vessel tumor", "cancer of great vessel of heart", "malignant great vessel neoplasm", "Malignant Great Vessel Neoplasm", "Malignant neoplasm of great vessels", "malignant neoplasm of great vessels", "malignant great vessel of heart neoplasm", "malignant neoplasm of great vessel of heart", "malignant neoplasm of great vessels (diagnosis)", "neoplasm - soft tissue types great vessels malignant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "great vessel cancer", "shortest_name_length": 19}
{"curie": "UMLS:C5418808", "names": ["Metastatic Endometrial Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Endometrial Serous Adenocarcinoma", "shortest_name_length": 44}
{"curie": "UMLS:C1335026", "names": ["Non-Neoplastic Oral Disease", "Non-Neoplastic Oral Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Oral Disorder", "shortest_name_length": 27}
{"curie": "UMLS:C4524746", "names": ["Postneoadjuvant Therapy Stage III Gastroesophageal Junction Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postneoadjuvant Therapy Stage III Gastroesophageal Junction Adenocarcinoma AJCC v8", "shortest_name_length": 82}
{"curie": "UMLS:C1336292", "names": ["Stage II Immature Testicular Teratoma", "Stage II Immature Testicular Teratoma AJCC v6", "Stage II Immature Testicular Teratoma AJCC v7", "Stage II Immature Testicular Teratoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Immature Testicular Teratoma AJCC v6 and v7", "shortest_name_length": 37}
{"curie": "MONDO:0030963", "names": ["LICAS", "Li-Campeau syndrome", "LI-CAMPEAU SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Li-Campeau syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0013687", "names": ["effusion", "Effusion", "EFFUSION", "Effusions", "effusions", "EFFUSIONS", "Free fluid", "free fluid", "Effusion, NOS", "Free fluid, NOS", "Effusion (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "effusion", "shortest_name_length": 8}
{"curie": "MONDO:0015853", "names": ["deficient breast volume or number"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deficient breast volume or number", "shortest_name_length": 33}
{"curie": "UMLS:C4330490", "names": ["Infratentorial and Spinal Cord Ependymal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infratentorial and Spinal Cord Ependymal Tumor", "shortest_name_length": 46}
{"curie": "UMLS:C2825116", "names": ["AML with Variant MLL Translocations", "Acute Myeloid Leukemia with Variant MLL Translocations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Myeloid Leukemia with Variant MLL Translocations", "shortest_name_length": 35}
{"curie": "UMLS:C0948780", "names": ["Rhinosinusitis", "rhinosinusitis", "Rhinosinusitis (disorder)", "rhinosinusitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rhinosinusitis", "shortest_name_length": 14}
{"curie": "UMLS:C0279917", "names": ["stage IV childhood HD", "childhood HD, stage IV", "pediatric HD, stage IV", "metastatic childhood HD", "HD, stage IV, childhood", "HD, childhood, stage IV", "pediatric HD, metastatic", "childhood HD, metastatic", "HD, metastatic, childhood", "HD, childhood, metastatic", "Stage IV Hodgkin Lymphoma", "Stage IV Pediatric Hodgkin Lymphoma", "stage IV childhood Hodgkin lymphoma", "Stage IV Childhood Hodgkin Lymphoma", "stage IV childhood Hodgkin's disease", "Pediatric Hodgkin's Disease Stage IV", "Childhood Hodgkin's Disease Stage IV", "pediatric Hodgkin's disease, stage IV", "Stage IV Childhood Hodgkin's Lymphoma", "Childhood Hodgkin's Lymphoma Stage IV", "Stage IV Pediatric Hodgkin's Lymphoma", "Pediatric Hodgkin's Lymphoma Stage IV", "stage IV Hodgkin's disease, childhood", "Hodgkin's disease, stage IV, childhood", "lymphoma, stage IV childhood Hodgkin's", "childhood Hodgkin's lymphoma, stage IV", "metastatic childhood Hodgkin's disease", "pediatric Hodgkin's disease, metastatic", "Hodgkin's lymphoma, stage IV, childhood", "metastatic Hodgkin's disease, childhood", "lymphoma, metastatic childhood Hodgkin's", "Hodgkin's disease, metastatic, childhood", "childhood Hodgkin's lymphoma, metastatic", "Hodgkin's lymphoma, metastatic, childhood", "Ann Arbor Stage IV Childhood Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Childhood Hodgkin Lymphoma", "shortest_name_length": 21}
{"curie": "MONDO:0019227", "names": ["disorder of glycerol metabolism", "inborn disorder of glycerol metabolism", "inborn glycerol metabolic process disorder", "inborn error of glycerol metabolic process", "rare inborn error of glycerol metabolic process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of glycerol metabolism", "shortest_name_length": 31}
{"curie": "MONDO:0042498", "names": ["Ruzicka-Goerz-Anton syndrome", "Ruzicka Goerz Anton syndrome", "Ichthyosis deafness mental retardation skeletal anomalies", "ichthyosis deafness mental retardation skeletal anomalies", "ichthyosis deafness intellectual disability skeletal anomalies", "ichthyosis congenita, neurosensory deafness, oligophrenia, dental aplasia, brachydactyly, clinodactyly, accessory cervical ribs and thyroid carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ruzicka-Goerz-Anton syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0042488", "names": ["cestodes", "Tapeworm", "tapeworm", "Cestodosis", "Cenuriases", "Cenuriasis", "Coenuriases", "CESTODIASIS", "cestodiasis", "Cestodiasis", "Coenuriasis", "Dipylidiasis", "Tapeworm NOS", "Dipylidiases", "Bertielliasis", "Bertielliases", "Raillietiniases", "Raillietiniasis", "Infection;cestode", "Cestode infection", "Cestode Infection", "cestode infection", "Infection, Cestode", "Tapeworm infection", "infection, cestode", "cestode infections", "Tapeworm Infection", "TAPEWORM INFECTION", "tapeworm infection", "Cestode Infections", "Cestode infections", "infection; cestodes", "Infection, Tapeworm", "infections, cestode", "infection, tapeworm", "Infections, Cestode", "Tapeworm Infections", "Cestode infestation", "cestode infestation", "cestodes; infection", "tapeworm infections", "Infections, Tapeworm", "infections, tapeworm", "cestodes; infestation", "infestation; cestodes", "infestation; tapeworm", "Cestode infection NOS", "tapeworm; infestation", "Disease due to Cestoda", "disease due to Cestoda", "Tapeworm infection NOS", "Cestode infection, NOS", "Tapeworm infection, NOS", "DISEASES DUE TO CESTODA", "Tapeworm (infection) NOS", "Cestoda infectious disease", "Cestode infectious disease", "Cestoda disease or disorder", "Cestode infection (disorder)", "cestode infection (diagnosis)", "Cestode infection, unspecified", "Cestoda caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cestode infectious disease", "shortest_name_length": 8}
{"curie": "MONDO:0021492", "names": ["benign Major salivary gland tumor", "Benign Major Salivary Gland Tumor", "Benign tumor major salivary gland", "Benign tumour major salivary gland", "Benign Tumor of Major Salivary Gland", "major salivary gland benign neoplasm", "benign tumor of Major salivary gland", "benign Major salivary gland neoplasm", "Benign Major Salivary Gland Neoplasm", "Benign neoplasm of major salivary gland", "benign neoplasm of major salivary gland", "Benign Neoplasm of Major Salivary Gland", "benign tumor of the Major salivary gland", "Benign Tumor of the Major Salivary Gland", "Benign neoplasm of major salivary glands", "benign neoplasm of the Major salivary gland", "Benign Neoplasm of the Major Salivary Gland", "Benign neoplasm of major salivary gland, NOS", "Benign neoplasm of major salivary gland (disorder)", "Benign neoplasm of major salivary gland, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of major salivary gland", "shortest_name_length": 33}
{"curie": "MONDO:0008043", "names": ["myoclonus cerebellar ataxia deafness", "Myoclonus, Cerebellar Ataxia, and Deafness", "myoclonus, cerebellar ataxia, and deafness", "MYOCLONUS, CEREBELLAR ATAXIA, AND DEAFNESS", "myoclonus-cerebellar ataxia-deafness syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myoclonus-cerebellar ataxia-deafness syndrome", "shortest_name_length": 36}
{"curie": "UMLS:C0413234", "names": ["allergic reaction acute", "ALLERGIC REACTION ACUTE", "Acute allergic reaction", "Acute allergic reaction (disorder)", "Acute allergic reaction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute allergic reaction", "shortest_name_length": 23}
{"curie": "UMLS:C1332985", "names": ["Pediatric NLPHD", "Childhood NLPHD", "Nodular Lymphocyte Predominant Hodgkin Lymphoma", "childhood nodular lymphocyte predominant Hodgkin lymphoma", "Childhood Nodular Lymphocyte Predominant Hodgkin Lymphoma", "Childhood Nodular Lymphocyte Predominant Hodgkin's Disease", "Pediatric Nodular Lymphocyte Predominant Hodgkin's Disease", "Pediatric Nodular Lymphocyte Predominant Hodgkin's Lymphoma", "Childhood Nodular Lymphocyte Predominant Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Nodular Lymphocyte Predominant Hodgkin Lymphoma", "shortest_name_length": 15}
{"curie": "MONDO:0012389", "names": ["MYP12", "Myopia 12", "myopia 12", "MYOPIA 12 (disorder)", "myopia 12, autosomal dominant", "MYOPIA 12, AUTOSOMAL DOMINANT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopia 12, autosomal dominant", "shortest_name_length": 5}
{"curie": "MONDO:0008200", "names": ["PARK1", "Parkinson's disease 1", "Lewy Body Parkinsonism", "Atypical Parkinson Disease", "ATYPICAL PARKINSON DISEASE", "atypical Parkinson disease", "Parkinson Disease, Familial, Type 1", "Parkinson disease autosomal dominant", "Parkinson disease, autosomal dominant", "Parkinson Disease, Autosomal Dominant", "autosomal dominant Parkinson disease 1", "PARKINSON DISEASE 1, AUTOSOMAL DOMINANT", "Parkinson disease 1, autosomal dominant", "autosomal dominant Parkinson's disease 1", "autosomal dominant Parkinson disease type 1", "Parkinson disease, autosomal dominant (diagnosis)", "PARKINSON DISEASE 1, AUTOSOMAL DOMINANT LEWY BODY", "Parkinson disease 1, autosomal dominant Lewy body", "PARKINSON DISEASE 1, AUTOSOMAL DOMINANT (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant Parkinson disease 1", "shortest_name_length": 5}
{"curie": "MONDO:0003241", "names": ["Hemangioma of CNS", "hemangioma of CNS", "Hemangioma of the CNS", "hemangioma of the CNS", "central nervous system hemangioma", "Central Nervous System Hemangioma", "Hemangioma of Central Nervous System", "hemangioma of central nervous system", "hemangioma of the central nervous system", "Hemangioma of the Central Nervous System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system hemangioma", "shortest_name_length": 17}
{"curie": "UMLS:C4525346", "names": ["IV", "Stage IV Hilar Cholangiocarcinoma", "Stage IV Hilar Cholangiocarcinoma AJCC v8", "Stage IV Perihilar Cholangiocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Hilar Cholangiocarcinoma AJCC v8", "shortest_name_length": 2}
{"curie": "MONDO:0024777", "names": ["IMD98", "INFLTR8", "X-linked immunodeficiency with autoinflammation", "immunodeficiency 98 with autoinflammation, X-linked", "IMMUNODEFICIENCY 98 WITH AUTOINFLAMMATION, X-LINKED", "INFLAMMATION, NEUTROPENIA, BONE MARROW FAILURE, AND LYMPHOPROLIFERATION CAUSED BY TLR8", "inflammation, neutropenia, bone marrow failure, and lymphoproliferation caused by TLR8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 98 with autoinflammation, X-linked", "shortest_name_length": 5}
{"curie": "UMLS:C4683422", "names": ["Tumor Stage (Pathologic)", "Thyroid Gland Papillary Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Papillary Carcinoma by AJCC v8 Stage", "shortest_name_length": 24}
{"curie": "UMLS:C4055021", "names": ["FSH-producing Adenoma", "FSH-Producing Pituitary Gland Adenoma", "FSH-Producing Pituitary Neuroendocrine Tumor", "Follicle Stimulating Hormone-Producing Adenoma", "Follicle Stimulating Hormone-Producing Gonadotroph Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FSH-Producing Pituitary Neuroendocrine Tumor", "shortest_name_length": 21}
{"curie": "MONDO:0030060", "names": ["NEDLIB", "neurodevelopmental disorder with language impairment and behavioral abnormalities", "NEURODEVELOPMENTAL DISORDER WITH LANGUAGE IMPAIRMENT AND BEHAVIORAL ABNORMALITIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with language impairment and behavioral abnormalities", "shortest_name_length": 6}
{"curie": "UMLS:C5446532", "names": ["Primary Uveal Lymphoma", "Primary Uveal Non-Hodgkin Lymphoma", "Uveal Reactive Lymphoid Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Uveal Non-Hodgkin Lymphoma", "shortest_name_length": 22}
{"curie": "UMLS:C0702163", "names": ["Trichorrhexis", "trichorrhexis", "Trichorrhexis, NOS", "Trichorrhexis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Trichorrhexis", "shortest_name_length": 13}
{"curie": "MONDO:0004463", "names": ["PMFPES", "Prefibrotic/Early Primary Myelofibrosis", "Prefibrotic/Early Primary myelofibrosis", "primary myelofibrosis, Prefibrotic stage", "Primary Myelofibrosis, Prefibrotic Stage", "Primary Myelofibrosis, Prefibrotic/Early Stage", "primary myelofibrosis, Prefibrotic/early stage", "cellular phase chronic idiopathic myelofibrosis", "chronic idiopathic myelofibrosis, cellular phase", "chronic idiopathic myelofibrosis, Prefibrotic stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cellular phase chronic idiopathic myelofibrosis", "shortest_name_length": 6}
{"curie": "UMLS:C2981680", "names": ["stage IIA prostate cancer", "Stage IIA Prostate Cancer", "stage IIA prostate cancer AJCC v7", "Stage IIA Prostate Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Prostate Cancer AJCC v7", "shortest_name_length": 25}
{"curie": "UMLS:C1512437", "names": ["High Grade Prostatic Intraepithelial Neoplasia, Mucinous Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Prostatic Intraepithelial Neoplasia, Mucinous Variant", "shortest_name_length": 64}
{"curie": "MONDO:0035667", "names": ["isolated optic neuritis without anti-MOG antibodies", "Isolated optic neuritis without anti-myelin oligodendrocyte glycoprotein antibodies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated optic neuritis without anti-MOG antibodies", "shortest_name_length": 51}
{"curie": "MONDO:0032896", "names": ["SPGF42", "spermatogenic failure 42", "SPERMATOGENIC FAILURE 42"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 42", "shortest_name_length": 6}
{"curie": "MONDO:0011735", "names": ["HIGM3", "HIGM3 Syndrome", "CD40 Deficiency", "HIGM3 Syndromes", "CD40 deficiency", "Hyper-IgM Syndrome 3", "hyper-IgM syndrome 3", "hyper IgM syndrome 3", "Hyper IgM Syndrome 3", "HYPER-IgM SYNDROME 3", "CD40 hyper-IgM syndrome", "hyper-IgM syndrome type 3", "Hyper-IgM syndrome type 3", "type 3 hyper-IgM immunodeficiency", "immunodeficiency with hyper-IgM type 3", "immunodeficiency with hyper IgM type 3", "Immunodeficiency with Hyper IgM, Type 3", "IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 3", "immunodeficiency with hyper-IgM, type 3", "Immunodeficiency with Hyper-IgM, Type 3", "Hyper-IgM syndrome due to CD40 deficiency", "hyper-IgM syndrome due to CD40 deficiency", "Hyper IgM Immunodeficiency Syndrome Type 3", "Hyper-IgM Immunodeficiency Syndrome Type 3", "Hyper-IgM Immunodeficiency Syndrome, Type 3", "Hyper IgM Immunodeficiency Syndrome, Type 3", "hyper-IgM syndrome caused by mutation in CD40"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyper-IgM syndrome type 3", "shortest_name_length": 5}
{"curie": "UMLS:C0852869", "names": ["elbow deformity", "Elbow deformity", "deformity; elbow", "elbow; deformity", "deformity of elbow", "Elbow deformity NOS", "deformity of elbow (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Elbow deformity", "shortest_name_length": 15}
{"curie": "MONDO:0003249", "names": ["pinealoma", "Pineal cancer", "pineocytic tumor", "Pineocytic tumor", "pineal body cancer", "pineal gland cancer", "pineal body neoplasm", "cancer of pineal body", "Cancer of pineal gland", "neoplasm of pineal gland", "Malignant pineal neoplasm", "tumor of the pineal region", "Malignant Pineal Area Tumor", "malignant pineal area tumor", "malignant pineal gland tumor", "Malignant Pineal Gland Tumor", "malignant Pineal Region tumor", "malignant pineal region tumor", "neoplasm of the Pineal Region", "Malignant Pineal Region Tumor", "neoplasm of the pineal region", "Malignant Pineal Area Neoplasm", "malignant pineal body neoplasm", "malignant pineal area neoplasm", "malignant pineal gland neoplasm", "Malignant Tumor of Pineal Gland", "Malignant tumor of pineal gland", "malignant tumor of pineal gland", "Malignant Pineal Gland Neoplasm", "Malignant tumour of pineal gland", "malignant pineal region neoplasm", "Malignant Pineal Region Neoplasm", "malignant neoplasm of pineal body", "malignant neoplasm of pineal gland", "Malignant Neoplasm of Pineal Gland", "Malignant neoplasm of pineal gland", "malignant tumor of the pineal gland", "Malignant Tumor of the Pineal Gland", "malignant neoplasm of the pineal gland", "Malignant Neoplasm of the Pineal Gland", "Malignant tumor of pineal gland (disorder)", "malignant neoplasm of endocrine glands pineal", "malignant neoplasm of pineal gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pineal gland cancer", "shortest_name_length": 9}
{"curie": "MONDO:0018731", "names": ["lethal multiple congenital anomalies/dysmorphic syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal multiple congenital anomalies/dysmorphic syndrome", "shortest_name_length": 56}
{"curie": "UMLS:C0521471", "names": ["LE RASH", "SLE rash", "DERMATITIS LUPOID", "Dermatitis lupoid", "Lupoid dermatitis", "LUPOID DERMATITIS", "SYSTEMIC ERYTHEMATOSUS RASH", "systemic lupus erythematosus rash", "Systemic lupus erythematosus rash", "Systemic Lupus Erythematosus Rash", "Rash of systemic lupus erythematosus", "systemic lupus erythematosus rash (diagnosis)", "Butterfly rash associated with systemic lupus", "Rash of systemic lupus erythematosus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Systemic lupus erythematosus rash", "shortest_name_length": 7}
{"curie": "UMLS:C0740278", "names": ["Pelvic peritoneal adhesion", "Pelvic peritoneal adhesions", "Adhesion of pelvic peritoneum", "Adhesion of pelvic peritoneum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adhesion of pelvic peritoneum", "shortest_name_length": 26}
{"curie": "UMLS:C0265115", "names": ["acute cerebrovascular insufficiency", "Acute cerebrovascular insufficiency", "Acute cerebrovascular insufficiency NOS", "Acute cerebrovascular insufficiency, NOS", "Acute cerebrovascular insufficiency (disorder)", "acute cerebrovascular insufficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute cerebrovascular insufficiency", "shortest_name_length": 35}
{"curie": "UMLS:C1334463", "names": ["Lymphohistiocytic Variant Anaplastic Large Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphohistiocytic Variant Anaplastic Large Cell Lymphoma", "shortest_name_length": 56}
{"curie": "MONDO:0018940", "names": ["CMS", "congenital MG", "congenital myasthenia", "Congenital Myasthenia", "erb-Goldflam syndrome", "Congenital myasthenia", "congenital; myasthenia", "Myasthenia, Congenital", "myasthenia; congenital", "Congenital Myasthenias", "Myasthenias, Congenital", "Gravi, Congenital Myasthenia", "congenital myasthenia gravis", "Congenital Myasthenia Gravis", "myasthenia gravis congenital", "Myasthenia Gravis, Congenital", "Congenital myasthenia syndrome", "Congenital myasthenic syndrome", "congenital myasthenic syndrome", "Congenital Myasthenic Syndrome", "familial limb-girdle myasthenia", "myasthenic syndrome, congenital", "Myasthenic Syndrome, Congenital", "congenital myasthenic syndromes", "Syndrome, Congenital Myasthenic", "Congenital Myasthenic Syndromes", "Syndromes, Congenital Myasthenic", "Myasthenic Syndromes, Congenital", "myasthenia gravis pseudoparalytica", "Congenital myasthenic syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myasthenic syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0002159", "names": ["Fallopian Tube Leiomyosarcoma", "fallopian tube leiomyosarcoma", "leiomyosarcoma of fallopian tube", "leiomyosarcoma of fallopian tube (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fallopian tube leiomyosarcoma", "shortest_name_length": 29}
{"curie": "MONDO:0009055", "names": ["CMTC", "Van Lohuizen syndrome", "Van Lohuizen's syndrome", "Congenital livedo reticularis", "Congenital livedo reticularis (disorder)", "Cutis marmorata telangiectasia congenita", "CUTIS MARMORATA TELANGIECTATICA CONGENITA", "Cutis marmorata telangiectatica congenita", "cutis marmorata telangiectatica congenita", "CMTC - Cutis marmorata telangiectatica congenita", "cutis marmorata telangiectatica congenita (disease)", "hereditary cutis marmorata telangiectatica congenita", "Hereditary cutis marmorata telangiectatica congenita", "cutis marmorata telangiectatica congenita (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutis marmorata telangiectatica congenita", "shortest_name_length": 4}
{"curie": "UMLS:C2063389", "names": ["retroperitoneal liposarcoma", "Retroperitoneal liposarcoma", "liposarcoma of retroperitoneum", "Liposarcoma of retroperitoneum", "Pelvic retroperitoneal liposarcoma", "Giant pelvic retroperitoneal liposarcoma", "Liposarcoma of retroperitoneum (disorder)", "liposarcoma of retroperitoneum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retroperitoneal liposarcoma", "shortest_name_length": 27}
{"curie": "MONDO:0002033", "names": ["cecal cancer", "Cecal cancer", "Cecal Cancer", "cecum cancer", "Cancer, Cecal", "Caecal cancer", "Cecum--Cancer", "caecal cancer", "caecum cancer", "cancer of cecum", "Cancer of Cecum", "Cancer of cecum", "Cancer of caecum", "cancer of caecum", "cancer of the cecum", "Cancer of the Cecum", "CA - Cancer of cecum", "CA - Cancer of caecum", "Malignant Cecum Tumor", "malignant cecum tumor", "malignant tumor of cecum", "malignant neoplasm cecum", "Malignant tumor of cecum", "Malignant Cecum Neoplasm", "Malignant Cecal Neoplasm", "Malignant Tumor of Cecum", "malignant cecum neoplasm", "malignant caecum neoplasm", "Malignant tumour of caecum", "Malignant neoplasm of cecum", "malignant neoplasm of cecum", "Malignant Neoplasm of Cecum", "Malignant neoplasm of caecum", "malignant neoplasm of caecum", "malignant tumor of the cecum", "Malignant Tumor of the Cecum", "malignant neoplasm of the cecum", "Malignant Neoplasm of the Cecum", "Malignant tumor of cecum (disorder)", "malignant neoplasm of cecum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cecum cancer", "shortest_name_length": 12}
{"curie": "MONDO:0010237", "names": ["Hyde Forster-McCarthy-Berry syndrome", "Hyde Forster McCarthy Berry syndrome", "Hyde Forster Mccarthy Berry syndrome", "plagiocephaly and X-linked mental retardation", "Plagiocephaly and X-linked mental retardation", "mental retardation, X-linked Hyde-Forster type", "Mental retardation, X-linked Hyde-Forster type", "Mental retardation, X-linked, Hyde-Forster type", "mental retardation, X-linked, Hyde-Forster type", "MENTAL RETARDATION, X-LINKED, HYDE-FORSTER TYPE", "plagiocephaly and X-linked intellectual disability", "intellectual disability, X-linked Hyde-Forster type", "intellectual disability, X-linked, Hyde-Forster type", "X-linked intellectual disability-plagiocephaly syndrome", "Mental retardation, X-linked, with craniofacial dysmorphism", "mental retardation, X-linked, with craniofacial dysmorphism", "MENTAL RETARDATION, X-LINKED, WITH CRANIOFACIAL DYSMORPHISM", "x-linked intellectual disability with plagiocephaly syndrome", "X-linked intellectual disability with plagiocephaly syndrome", "intellectual disability, X-linked, with craniofacial dysmorphism", "X-linked intellectual disability with plagiocephaly syndrome (disorder)", "x-linked intellectual disability with plagiocephaly syndrome (diagnosis)", "mental retardation, plagiocephaly, brachycephaly, prominent forehead, and coarse facial features", "Mental retardation, plagiocephaly, brachycephaly, prominent forehead, and coarse facial features", "intellectual disability, plagiocephaly, brachycephaly, prominent forehead, and coarse facial features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability-plagiocephaly syndrome", "shortest_name_length": 36}
{"curie": "MONDO:0008268", "names": ["PMS", "pms", "Menstrual molimen", "SYNDROME PREMENSTRUAL", "Syndrome premenstrual", "premenstrual syndrome", "PREMENSTRUAL SYNDROME", "Premenstrual syndrome", "Premenstrual Syndrome", "premenstrual syndromes", "Premenstrual Syndromes", "Syndrome, Premenstrual", "Syndromes, Premenstrual", "Czeizel Brooser syndrome", "Czeizel-Brooser syndrome", "pms premenstrual syndrome", "polydactyly myopia syndrome", "Polydactyly-Myopia Syndrome", "Polydactyly myopia syndrome", "POLYDACTYLY-MYOPIA SYNDROME", "polydactyly-myopia syndrome", "Polydactyly-myopia syndrome", "PMS - Premenstrual syndrome", "Premenstrual syndrome - PMS", "premenstrual syndrome (PMS)", "premenstrual syndromes (diagnosis)", "Polydactyly myopia syndrome (disorder)", "Postaxial Polydactyly with progressive myopia", "postaxial polydactyly with progressive myopia", "POLYDACTYLY, POSTAXIAL, WITH PROGRESSIVE MYOPIA", "polydactyly, postaxial, with progressive myopia", "Polydactyly, Postaxial, With Progressive Myopia", "Postaxial polydactyly-progressive myopia syndrome", "postaxial polydactyly-progressive myopia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polydactyly-myopia syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C5205251", "names": ["Ileal NET G2", "Ileal Neuroendocrine Tumor G2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ileal Neuroendocrine Tumor G2", "shortest_name_length": 12}
{"curie": "MONDO:0017879", "names": ["HARDS", "Hantavirus", "four corners hantavirus", "hantavirus pulmonary syndrome", "Hantavirus pulmonary syndrome", "Hantavirus Pulmonary Syndrome", "Hantavirus pulmonary infection", "Hanta virus pulmonary syndrome", "Hantavirus Pulmonary Syndromes", "Hantavirus disease pulmonary syndrome", "Hantavirus pulmonary syndrome (disorder)", "Hantavirus disease pulmonary syndrome (diagnosis)", "Hantavirus Associated Respiratory Distress Syndrome", "Hantavirus-Associated Respiratory Distress Syndrome", "Hantavirus-associated respiratory distress syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hantavirus pulmonary syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C4527182", "names": ["Stage IIB", "Stage IIB Cutaneous (Skin) Melanoma", "Pathologic Stage IIB Cutaneous Melanoma AJCC v8", "Pathologic Stage IIB Melanoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IIB Cutaneous Melanoma AJCC v8", "shortest_name_length": 9}
{"curie": "MONDO:0001456", "names": ["Pavingstone degeneration", "Cobblestone degeneration", "Paving stone degeneration", "Cobblestone retinal degeneration", "Pavingstone retinal degeneration", "cobblestone retinal degeneration", "Paving-stone retinal degeneration", "Paving stone retinal degeneration", "paving stone retinal degeneration", "paving stone degeneration of retina", "Paving stone degeneration of retina", "paving stone peripheral retinal degeneration", "Paving stone retinal degeneration (disorder)", "paving stone retinal degeneration (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cobblestone retinal degeneration", "shortest_name_length": 24}
{"curie": "MONDO:0003453", "names": ["conjunctiva intraepithelial neoplasia", "Conjunctiva Intraepithelial Neoplasia", "conjunctival intraepithelial neoplasm", "Conjunctival intraepithelial neoplasia", "conjunctival intraepithelial neoplasia", "Conjunctival Intraepithelial Neoplasia", "Intraepithelial Neoplasia of Conjunctiva", "intraepithelial neoplasia of conjunctiva", "Intraepithelial Neoplasia of the Conjunctiva", "intraepithelial neoplasia of the conjunctiva", "CIN - conjunctival intraepithelial neoplasia", "Conjunctival Squamous Intraepithelial Neoplasia", "Conjunctival intraepithelial neoplasia (disorder)", "conjunctival intraepithelial neoplasia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "conjunctival intraepithelial neoplasm", "shortest_name_length": 37}
{"curie": "MONDO:0025622", "names": ["CMTMA1", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, MITOCHONDRIAL FORM, 1", "Charcot-Marie-Tooth disease, axonal, mitochondrial form, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease, axonal, mitochondrial form, 1", "shortest_name_length": 6}
{"curie": "MONDO:0009721", "names": ["NATHALIE SYNDROME", "Nathalie syndrome", "Deafness-cataract-skeletal anomalies syndrome", "deafness-cataract-skeletal anomalies syndrome", "deafness-cataracts-skeletal anomalies syndrome", "Deafness with cataract and skeletal anomaly syndrome", "Deafness with cataract and skeletal anomaly syndrome (disorder)", "Sensorineural hearing loss-cataract-skeletal anomalies-cardiomyopathy syndrome", "sensorineural hearing loss-cataract-skeletal anomalies-cardiomyopathy syndrome", "deafness, cataract, muscular atrophy, skeletal abnormalities, growth retardation, underdeveloped secondary sexual characteristics"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nathalie syndrome", "shortest_name_length": 17}
{"curie": "UMLS:C4725847", "names": ["Recurrent Myxoid Liposarcoma", "Recurrent Myxoid/Round Cell Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Myxoid Liposarcoma", "shortest_name_length": 28}
{"curie": "UMLS:C0151623", "names": ["Hemorrhagic enterocolitis", "ENTEROCOLITIS HEMORRHAGIC", "enterocolitis hemorrhagic", "Enterocolitis hemorrhagic", "HEMORRHAGIC ENTEROCOLITIS", "hemorrhagic enterocolitis", "enterocolitis; hemorrhagic", "Haemorrhagic enterocolitis", "hemorrhagic; enterocolitis", "Enterocolitis haemorrhagic", "enterocolitis haemorrhagic", "Hemorrhagic enterocolitis (disorder)", "hemorrhagic enterocolitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemorrhagic enterocolitis", "shortest_name_length": 25}
{"curie": "MONDO:0003579", "names": ["Nerve fiber bundle defect", "nerve fibre bundle defect", "Nerve fibre bundle defect", "Retinal nerve fiber bundle defects", "retinal nerve fibre layer disorder", "retinal nerve fiber bundle defects", "nerve fiber layer of retina disease", "Nerve fiber bundle defect (disorder)", "Retinal nerve fibre bundle deficiency", "retinal nerve fiber bundle deficiency", "Retinal nerve fiber bundle deficiency", "disease of nerve fiber layer of retina", "disorder of nerve fiber layer of retina", "retinal nerve fiber bundle defects (diagnosis)", "nerve fiber layer of retina disease or disorder", "Retinal nerve fiber bundle deficiency (disorder)", "retinal nerve fiber bundle deficiency (diagnosis)", "disease or disorder of nerve fiber layer of retina"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal nerve fibre layer disorder", "shortest_name_length": 25}
{"curie": "UMLS:C4727378", "names": ["Recurrent Clear Cell Renal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Clear Cell Renal Cell Carcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0016836", "names": ["Del(16)(p13.11)", "Monosomy 16p13.11", "monosomy 16p13.11", "16p13.11 microdeletion syndrome", "16p13.11 microdeletion syndrome (disorder)", "16p13.11 recurrent microdeletion (neurocognitive disorder susceptibility locus)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "16p13.11 microdeletion syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0007983", "names": ["MCDS", "Schmid type metaphyseal dysplasia", "Metaphyseal dysplasia, Schmid type", "Schmid metaphyseal chondrodysplasia", "Metaphyseal dysostosis, Schmid type", "Metaphyseal chondrodysplasia Schmid type", "metaphyseal chondrodysplasia Schmid type", "Metaphyseal Chondrodysplasia, Schmid Type", "METAPHYSEAL CHONDRODYSPLASIA, SCHMID TYPE", "Metaphyseal chondrodysplasia, Schmid type", "metaphyseal chondrodysplasia, Schmid type", "Japanese type spondylometaphyseal dysplasia", "spondylometaphyseal dysplasia, Japanese type", "Spondylometaphyseal Dysplasia, Japanese Type", "SPONDYLOMETAPHYSEAL DYSPLASIA, JAPANESE TYPE", "Schmid's metaphyseal chondrodysplasia syndrome", "Metaphyseal chondrodysplasia, Schmid type (disorder)", "Metaphyseal chondrodysplasia, Schmid type (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Schmid metaphyseal chondrodysplasia", "shortest_name_length": 4}
{"curie": "MONDO:0018450", "names": ["SMARD2", "diaphragmatic spinal muscular atrophy type 2", "spinal muscular atrophy with respiratory distress type 2", "X-linked spinal muscular atrophy with respiratory distress", "severe infantile axonal neuropathy with respiratory failure type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal muscular atrophy with respiratory distress type 2", "shortest_name_length": 6}
{"curie": "MONDO:0017986", "names": ["disorder of plasmalogens biosynthesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of plasmalogens biosynthesis", "shortest_name_length": 37}
{"curie": "MONDO:0003581", "names": ["embryonal carcinoma", "ovary embryonal carcinoma", "Ovarian embryonal carcinoma", "ovarian embryonal carcinoma", "Ovarian Embryonal Carcinoma", "embryonal carcinoma of ovary", "Embryonal carcinoma of ovary", "embryonal carcinoma, ovarian", "Embryonal Carcinoma of Ovary", "Embryonal Carcinoma of the Ovary", "embryonal carcinoma of the ovary", "Embryonal carcinoma of the Ovary", "Embryonal carcinoma of ovary (disorder)", "embryonal carcinoma of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian embryonal carcinoma", "shortest_name_length": 19}
{"curie": "UMLS:C3831090", "names": ["Class 1a Uveal Melanoma", "Uveal Class 1a Melanoma", "Uveal Class 1a  Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uveal Class 1a Melanoma", "shortest_name_length": 23}
{"curie": "MONDO:0013803", "names": ["LCC", "Labrune Syndrome", "Labrune syndrome", "LABRUNE SYNDROME", "Leucoencephalopathy with calcifications and cysts", "leukoencephalopathy with calcifications and cysts", "Leukoencephalopathy with calcifications and cysts", "Leukoencephalopathy Brain Calcifications and Cysts", "LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS", "leukoencephalopathy, brain calcifications, and cysts", "Leukoencephalopathy with calcifications and cysts (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukoencephalopathy with calcifications and cysts", "shortest_name_length": 3}
{"curie": "UMLS:C2931877", "names": ["Preeclamptic toxemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Preeclamptic toxemia", "shortest_name_length": 20}
{"curie": "MONDO:0018431", "names": ["cold-induced sweating syndrome - hyperthermia spectrum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cold-induced sweating syndrome - hyperthermia spectrum", "shortest_name_length": 54}
{"curie": "MONDO:0600025", "names": ["hydrosalpinx", "Hydrosalpinx", "HYDROSALPINX", "blocked fallopian tube", "Hydrosalpinx (disease)", "Hydrosalpinx (disorder)", "hydrosalpinx (diagnosis)", "fallopian tube obstruction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hydrosalpinx", "shortest_name_length": 12}
{"curie": "UMLS:C0855204", "names": ["Stage III Testicular Mixed Germ Cell Tumor", "Testicular germ cell tumor mixed stage III", "Testicular germ cell tumour mixed stage III", "Stage III Testicular Mixed Germ Cell Tumor AJCC v7", "Stage III Testicular Mixed Germ Cell Tumor AJCC v6", "Stage III Testicular Mixed Germ Cell Tumor AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular germ cell tumor mixed stage III", "shortest_name_length": 42}
{"curie": "UMLS:C0151624", "names": ["ulcerative enterocolitis", "Enterocolitis ulcerative", "ENTEROCOLITIS ULCERATIVE", "Ulcerative enterocolitis", "ULCERATIVE ENTEROCOLITIS", "enterocolitis; ulcerative", "ulcerative; enterocolitis", "Ulcerative enterocolitis (disorder)", "ulcerative enterocolitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ulcerative enterocolitis", "shortest_name_length": 24}
{"curie": "UMLS:C4329673", "names": ["Stage I HPV-Mediated (p16-Positive) Oropharyngeal Throat Cancer", "Clinical Stage I HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage I HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8", "shortest_name_length": 63}
{"curie": "UMLS:C0877267", "names": ["Peritonsillitis", "peritonsillitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peritonsillitis", "shortest_name_length": 15}
{"curie": "MONDO:0040502", "names": ["GCCD5", "GLUCOCORTICOID DEFICIENCY 5", "glucocorticoid deficiency 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glucocorticoid deficiency 5", "shortest_name_length": 5}
{"curie": "MONDO:0021470", "names": ["pancreas tumor benign", "Benign Pancreas Tumor", "benign pancreas tumor", "Pancreas Tumor, Benign", "pancreas tumor, benign", "benign pancreatic tumor", "Benign Pancreatic Tumor", "Benign Pancreas Neoplasm", "benign pancreas neoplasm", "benign tumor of pancreas", "pancreas benign neoplasm", "pancreatic tumor, benign", "Benign Tumor of Pancreas", "Benign tumor of pancreas", "Pancreatic Tumor, Benign", "benign tumour of pancreas", "Benign tumour of pancreas", "Pancreas Neoplasm, Benign", "pancreas neoplasm, benign", "Benign Pancreatic Neoplasm", "Benign pancreatic neoplasm", "benign pancreatic neoplasm", "benign neoplasm of pancreas", "Benign neoplasm of pancreas", "Benign Neoplasm of Pancreas", "pancreatic neoplasm, benign", "Pancreatic Neoplasm, Benign", "Benign Tumor of the Pancreas", "benign tumor of the pancreas", "Benign pancreatic neoplasm NOS", "Benign Pancreatic Neoplasm NOS", "benign neoplasm of the pancreas", "Benign Neoplasm of the Pancreas", "Benign neoplasm of pancreas, NOS", "Benign neoplasm of pancreas (disorder)", "benign neoplasm of pancreas (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of pancreas", "shortest_name_length": 21}
{"curie": "UMLS:C4725794", "names": ["Metastatic Renal Pelvis Urothelial Cancer", "Metastatic Renal Pelvis Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Renal Pelvis Urothelial Carcinoma", "shortest_name_length": 41}
{"curie": "UMLS:C0854402", "names": ["Mechanical complication of implant", "Mechanical complication of implant (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mechanical complication of implant", "shortest_name_length": 34}
{"curie": "MONDO:0019925", "names": ["UPD(21)pat", "Paternal uniparental disomy of chromosome 21", "paternal uniparental disomy of chromosome 21", "paternal uniparental disomy of chromosome type 21", "Paternal uniparental disomy of chromosome 21 (disorder)", "Paternal uniparental disomy of chromosome 21 (diagnosis)", "anomaly of chromosome pair paternal uniparental disomy chromosome 21"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paternal uniparental disomy of chromosome 21", "shortest_name_length": 10}
{"curie": "MONDO:0015197", "names": ["SVA", "aortic sinus aneurysm", "Aortic sinus aneurysm", "sinus valsalva aneurysm", "aneurysm sinus valsalva", "aneurysm of sinus valsalva", "Sinus of Valsalva aneurysm", "sinus of Valsalva aneurysm", "sinus of valsalva aneurysm", "Aneurysm of the aortic sinus", "aneurysm of sinus of Valsalva", "Aneurysm of sinus of Valsalva", "aneurysm of sinus of valsalva", "aortic sinus aneurysm (diagnosis)", "Dilatation of the sinus of Valsalva", "Congenital aneurysm of sinus of Valsalva", "aneurysm of sinus of Valsalva (diagnosis)", "Congenital aneurysm of sinus of Valsalva (disorder)", "Congenital aneurysm of sinus of Valsalva (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aneurysm of sinus of Valsalva", "shortest_name_length": 3}
{"curie": "UMLS:C0272688", "names": ["closed fracture of metacarpal neck", "closed fracture of neck of metacarpal", "closed fracture of neck of metacarpal bone", "Closed Fracture of Neck of Metacarpal Bone", "Closed fracture of neck of metacarpal bone", "Closed fracture of neck of metacarpal bones", "Closed fracture of neck of metacarpal bone(s)", "Closed fracture of neck of metacarpal bone (disorder)", "closed fracture of neck of metacarpal bone (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Closed fracture of neck of metacarpal bone", "shortest_name_length": 34}
{"curie": "MONDO:0021543", "names": ["gum angioma", "Gum Angioma", "Angioma of Gum", "gum hemangioma", "Gum Hemangioma", "angioma of gum", "Gingival Angioma", "gingival angioma", "Hemangioma of Gum", "hemangioma of gum", "angioma of gingiva", "angioma of the gum", "Angioma of Gingiva", "gingiva hemangioma", "Angioma of the Gum", "gingival hemangioma", "Gingival Hemangioma", "GINGIVAL HEMANGIOMA", "Hemangioma of Gingiva", "Hemangioma of gingiva", "hemangioma of gingiva", "Hemangioma of the Gum", "hemangioma of the gum", "angioma of the gingiva", "Angioma of the Gingiva", "Haemangioma of gingiva", "hemangioma of the gingiva", "Hemangioma of the Gingiva", "Hemangioma of gingiva (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemangioma of gingiva", "shortest_name_length": 11}
{"curie": "UMLS:C0152499", "names": ["Acute amebiasis", "amebiasis acute", "Acute amoebiasis", "acute; amebiasis", "amebiasis; acute", "Acute amebiasis (disorder)", "Acute amebiasis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute amebiasis", "shortest_name_length": 15}
{"curie": "UMLS:C0751115", "names": ["Moore", "Digestive Epilepsy", "Abdominal Epilepsy", "Epilepsy, Abdominal", "epilepsy; abdominal", "abdominal; epileptic", "Digestive Epilepsies", "Abdominal Epilepsies", "Epilepsies, Abdominal", "Epilepsies, Digestive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Digestive Epilepsy", "shortest_name_length": 5}
{"curie": "MONDO:0016748", "names": ["HMBL", "Angioblastoma", "angioblastoma", "Hemangioblastoma", "HEMANGIOBLASTOMA", "hemangioblastoma", "haemangioblastoma", "Haemangioblastoma", "Hemangioblastomas", "hemangioblastomas", "Capillary Hemangioblastoma", "capillary hemangioblastoma", "Hemangioblastoma (disorder)", "Hemangioblastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemangioblastoma", "shortest_name_length": 4}
{"curie": "MONDO:0006972", "names": ["Silo-fillers' lung", "silo filler disease", "Silo Filler Disease", "SILO FILLER DISEASE", "Silo Fillers Disease", "silo fillers disease", "Disease, Silo Filler", "disease silo fillers", "Silo-workers' asthma", "Silo-filler's disease", "Silo Filler's Disease", "Silo filler's disease", "Disease, Silo Fillers", "Silo-fillers' disease", "Silo Fillers' Disease", "silo fillers' disease", "silo-filler's disease", "silo-fillers' disease", "silo filler's disease", "Disease, Silo Fillers'", "silo-filler's; disease", "Disease, Silo Filler's", "PNEUMONOSIS, SILO FILLER", "PNEUMONIA, NITROGEN DIOXIDE", "Silo-fillers' disease (disorder)", "silo fillers' disease (diagnosis)", "disease (or disorder); silo-filler's"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "silo filler disease", "shortest_name_length": 18}
{"curie": "MONDO:0008463", "names": ["Split-Hand And Split-Foot With Hypodontia", "split-hand and split-foot with hypodontia", "SPLIT-HAND AND SPLIT-FOOT WITH HYPODONTIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "split-hand and split-foot with hypodontia", "shortest_name_length": 41}
{"curie": "MONDO:0003042", "names": ["Adult Mesenchymal Chondrosarcoma", "adult mesenchymal chondrosarcoma", "mesenchymal chondrosarcoma of adults"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult mesenchymal chondrosarcoma", "shortest_name_length": 32}
{"curie": "MONDO:0018168", "names": ["primary non-essential cutis verticis gyrata"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary non-essential cutis verticis gyrata", "shortest_name_length": 43}
{"curie": "MONDO:0060640", "names": ["NEDMEBA", "neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy", "NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, EPILEPSY, AND BRAIN ATROPHY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy", "shortest_name_length": 7}
{"curie": "MONDO:0004960", "names": ["Paraproteinemia", "paraproteinemia", "paraproteinemias", "Paraproteinaemia", "paraproteinaemia", "Paraproteinemias", "Paraproteinemia NOS", "Paraproteinaemia NOS", "GAMMOPATHY MONOCLONAL", "gammopathy monoclonal", "MONOCLONAL GAMMOPATHY", "Monoclonal Gammapathy", "Monoclonal Gammopathy", "monoclonal gammopathy", "gammapathy monoclonal", "Monoclonal gammopathy", "monoclonal gammapathy", "Gammapathy, Monoclonal", "monoclonal; gammopathy", "gammopathy; monoclonal", "Gammopathy, Monoclonal", "Paraimmunoglobulinemia", "Monoclonal gammopathies", "monoclonal gammapathies", "gammopathies monoclonal", "Monoclonal Gammapathies", "Paraimmunoglobulinemias", "monoclonal gammopathies", "Monoclonal Gammopathies", "Monoclonal gammopathy NOS", "Monoclonal Paraproteinemia", "Monoclonal paraproteinemia", "Monoclonal paraproteinaemia", "Monoclonal gammopathy (clinical)", "Monoclonal gammopathy (disorder)", "Monoclonal hypergammaglobulinemia", "monoclonal gammopathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "monoclonal gammopathy", "shortest_name_length": 15}
{"curie": "MONDO:0001672", "names": ["bronchus cancer", "cancer of bronchus", "Neoplasm malig;bronchus", "Malignant tumor of bronchus", "malignant bronchus neoplasm", "Malignant tumour of bronchus", "Malignant Bronchial Neoplasm", "Malignant Neoplasm of Bronchus", "Malignant neoplasm of bronchus", "malignant neoplasm of bronchus", "lung neoplasm malignant bronchus", "Malignant neoplasm bronchus/lung", "malignant neosplasm of the bronchus", "Malignant neoplasm of bronchus, NOS", "malignant neoplasm of bronchus or lung", "Malignant tumor of bronchus (disorder)", "Malignant neoplasm of bronchus and lung", "malignant neoplasm of bronchus and lung", "malignant neoplasm of bronchus (diagnosis)", "Malignant neoplasm of bronchus or lung, unspecified", "malignant neoplasm of bronchus and lung, unspecified", "Malignant neoplasm of bronchus and lung, unspecified", "Malignant neoplasm of unspecified part of bronchus or lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bronchus cancer", "shortest_name_length": 15}
{"curie": "MONDO:0018069", "names": ["Trisomy 17qter", "trisomy 17qter", "Distal trisomy 17q", "distal trisomy 17q", "Distal duplication 17q", "distal duplication 17q", "distal trisomy type 17q", "Telomeric duplication 17q", "telomeric duplication 17q", "Distal trisomy 17q syndrome", "Distal trisomy 17q syndrome (disorder)", "Distal trisomy 17q syndrome (diagnosis)", "anomaly of chromosome pair 17 partial trisomy 17q distal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal trisomy 17q", "shortest_name_length": 14}
{"curie": "MONDO:0011393", "names": ["FHA", "FHD", "HDLD", "HDLCQ13", "familial HDL deficiency", "HDL cholesterol, Low serum", "HDL deficiency, familial, 1", "hypoalphalipoproteinemia, primary", "familial hypoalphalipoproteinemia", "primary hypoalphalipoproteinemia 1", "hypoalphalipoproteinemia, familial", "high density lipoprotein deficiency", "HYPOALPHALIPOPROTEINEMIA, PRIMARY, 1", "hypoalphalipoproteinemia, primary, 1", "HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 13"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypoalphalipoproteinemia, primary, 1", "shortest_name_length": 3}
{"curie": "MONDO:0012733", "names": ["ARB", "BESTROPHINOPATHY", "Bestrophinopathy", "bestrophinopathy", "Retinopathy Burgess Black type", "retinopathy, Burgess-Black type", "Retinopathy, Burgess-Black type", "autosomal recessive bestrophinopathy", "Autosomal recessive bestrophinopathy", "bestrophinopathy, autosomal recessive", "BESTROPHINOPATHY, AUTOSOMAL RECESSIVE", "Autosomal recessive bestrophinopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive bestrophinopathy", "shortest_name_length": 3}
{"curie": "MONDO:0019628", "names": ["Rieger anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rieger anomaly", "shortest_name_length": 14}
{"curie": "UMLS:C2363809", "names": ["Incessant ventricular tachycardia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Incessant ventricular tachycardia", "shortest_name_length": 33}
{"curie": "MONDO:0019179", "names": ["monosomy 9q22.3", "Monosomy 9q22.3", "9q22.3 Deletion", "microdeletion 9q22.3", "Microdeletion 9q22.3", "9q22.3 Microdeletion", "9q22 Deletion Syndrome", "9q22.3 deletion syndrome", "Monosomy 9q22.3 syndrome", "Microdeletion 9q22.3 Syndrome", "Monosomy 9q22.3 syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "monosomy 9q22.3", "shortest_name_length": 15}
{"curie": "MONDO:0006154", "names": ["Colon MALToma", "colon MALToma", "colonic MALToma", "Colonic MALToma", "MALToma of colon", "MALToma of Colon", "Colon MALT Lymphoma", "colon MALT lymphoma", "MALToma of the Colon", "MALToma of the colon", "colonic MALT lymphoma", "Colonic MALT Lymphoma", "MALT lymphoma of colon", "MALT Lymphoma of Colon", "MALT Lymphoma of the Colon", "MALT lymphoma of the colon", "Colon Mucosa-Associated Lymphoid Tissue Lymphoma", "colon mucosa-associated lymphoid tissue lymphoma", "Colonic Mucosa-Associated Lymphoid Tissue Lymphoma", "colonic mucosa-associated lymphoid tissue lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colon mucosa-associated lymphoid tissue lymphoma", "shortest_name_length": 13}
{"curie": "UMLS:C4053714", "names": ["adult malignant fibrous histiocytoma of bone", "Adult Malignant Fibrous Histiocytoma of Bone", "Malignant fibrous histiocytoma of bone, adult", "Adult Undifferentiated High Grade Pleomorphic Sarcoma", "Undifferentiated High Grade Pleomorphic Sarcoma of Bone", "Adult Undifferentiated High Grade Pleomorphic Sarcoma of Bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Undifferentiated High Grade Pleomorphic Sarcoma of Bone", "shortest_name_length": 44}
{"curie": "MONDO:0021017", "names": ["synaptopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "synaptopathy", "shortest_name_length": 12}
{"curie": "UMLS:C5556741", "names": ["Vaginal Adenocarcinoma of Skene Gland Origin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Adenocarcinoma of Skene Gland Origin", "shortest_name_length": 44}
{"curie": "MONDO:0013500", "names": ["IMD51", "CANDF5", "CANDF5, FORMERLY", "IMMUNODEFICIENCY 51", "immunodeficiency 51", "familial candidiasis 5", "candidiasis, familial, 5", "candidiasis, familial, type 5", "candidiasis, familial, 5, formerly", "CANDIDIASIS, FAMILIAL, 5, FORMERLY", "candidiasis, familial chronic mucocutaneous, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 51", "shortest_name_length": 5}
{"curie": "MONDO:0035819", "names": ["CIMDAG", "CIMDAG syndrome", "CIMDAG SYNDROME", "cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome", "Cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome", "CEREBELLAR HYPOPLASIA, CATARACTS, IMPAIRED INTELLECTUAL DEVELOPMENT, CONGENITAL MICROCEPHALY, DYSTONIA, DYSERYTHROPOIETIC ANEMIA, AND GROWTH RETARDATION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0012634", "names": ["HMMS", "HAMAMY syndrome", "Hamamy syndrome", "HAMAMY SYNDROME", "Craniofacial dysplasia osteopenia syndrome", "craniofacial dysplasia - osteopenia syndrome", "Craniofacial dysplasia osteopenia syndrome (disorder)", "hypertelorism, Severe, with midface prominence, myopia, mental retardation, and bone fragility", "Hypertelorism, Severe, With Midface Prominence, Myopia, Mental Retardation, And Bone Fragility", "HYPERTELORISM, SEVERE, WITH MIDFACE PROMINENCE, MYOPIA, MENTAL RETARDATION, AND BONE FRAGILITY", "Facial dysmorphism-ocular anomalies-osteopenia-intellectual disability-dental anomalies syndrome", "hypertelorism, Severe, with midface prominence, myopia, intellectual disability, and bone fragility"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniofacial dysplasia - osteopenia syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0004543", "names": ["enteric pattern testicular yolk sac tumor", "Testicular Yolk Sac Tumor, Enteric Pattern", "testicular yolk Sac tumor, enteric pattern"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "enteric pattern testicular yolk sac tumor", "shortest_name_length": 41}
{"curie": "UMLS:C0700613", "names": ["ANXIETY STATE", "anxiety state", "Anxiety state", "state anxiety", "state; anxiety", "Anxiety states", "anxiety; state", "Anxiety state (finding)", "Anxiety state, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anxiety state", "shortest_name_length": 13}
{"curie": "MONDO:0018865", "names": ["striate palmoplantar keratoderma", "Striate palmoplantar keratoderma", "Keratosis palmoplantaris striata", "keratosis palmoplantaris striata", "keratosis palmoplantaris striata et areata", "Keratosis palmoplantaris striata et areata", "hereditary palmoplantar keratoderma striate", "Striate palmoplantar keratoderma (disorder)", "Striate palmoplantar keratoderma (diagnosis)", "Keratosis palmoplantaris varians of Wachters", "keratosis palmoplantaris varians of Wachters"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "striate palmoplantar keratoderma", "shortest_name_length": 32}
{"curie": "MONDO:0015390", "names": ["proboscis lateralis", "Proboscis lateralis", "congenital tubular nose", "Congenital tubular nose", "Proboscis lateralis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "proboscis lateralis", "shortest_name_length": 19}
{"curie": "MONDO:0016323", "names": ["chronic respiratory distress with surfactant metabolism deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic respiratory distress with surfactant metabolism deficiency", "shortest_name_length": 66}
{"curie": "MONDO:0009662", "names": ["MPS7", "MPS 7", "MPSVII", "MPS VII", "Sly Disease", "sly disease", "Sly disease", "Sly Syndrome", "SLY SYNDROME", "Disease, Sly", "Sly syndrome", "sly syndrome", "Syndrome, Sly", "GUS deficiency", "Sly's syndrome", "Gus deficiency", "GUSB Deficiency", "GUSB deficiency", "gusb deficiency", "Gusb deficiency", "GUSB DEFICIENCY", "Deficiency, GUSB", "GUSB Deficiencies", "Deficiencies, GUSB", "MPS VII - Sly syndrome", "Mucopolysaccharidosis 7", "MUCOPOLYSACCHARIDOSIS VII", "mucopolysaccharidosis VII", "Mucopolysaccharidosis VII", "B glucuronidase deficiency", "Mucopolysaccharidosis VIIs", "VIIs, Mucopolysaccharidosis", "Mucopolysaccharidosis type 7", "mucopolysaccharidosis type 7", "Beta-Glucuronidase Deficiency", "beta Glucuronidase Deficiency", "beta-glucuronidase deficiency", "beta-Glucuronidase deficiency", "mucopolysaccharidosis, type 7", "beta-Glucuronidase Deficiency", "BETA-GLUCURONIDASE DEFICIENCY", "Beta-glucuronidase deficiency", "mucopolysaccharidosis type VII", "deficiency; beta-glucuronidase", "Deficiency, beta-Glucuronidase", "Mucopolysaccharidosis Type VII", "mucopolysaccharidosis, mps-VII", "Mucopolysaccharidosis type VII", "Mucopolysaccharidosis, MPS-VII", "beta-glucoronidase; deficiency", "mucopolysaccharidosis (MPS) VII", "Type VII, Mucopolysaccharidosis", "beta-Glucuronidase Deficiencies", "type VII; mucopolysaccharidosis", "mucopolysaccharidosis, type VII", "MUCOPOLYSACCHARIDOSIS, TYPE VII", "Mucopolysaccharidosis Type VIIs", "Deficiencies, beta-Glucuronidase", "deficiency of beta-glucuronidase", "Type VIIs, Mucopolysaccharidosis", "Deficiency of beta-glucuronidase", "MPS VII - mucopolysaccharidosis VII", "MPS VII - Mucopolysaccharidosis VII", "mucopolysaccharide storage disease VII", "Mucopolysaccharidosis type VII (disorder)", "mucopolysaccharidosis type VII (diagnosis)", "Deficiency of beta-glucuronidase (disorder)", "beta-glucuronidase deficiency mucopolysaccharidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucopolysaccharidosis type 7", "shortest_name_length": 4}
{"curie": "MONDO:0015568", "names": ["isolated apertura pyriformis stenosis", "isolated nasal pyriform aperture hypoplasia", "isolated congenital nasal pyriform aperture stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated congenital nasal pyriform aperture stenosis", "shortest_name_length": 37}
{"curie": "MONDO:0010687", "names": ["XRN", "NPHL1", "NEPHROLITHIASIS 1", "Nephrolithiasis 1", "nephrolithiasis 1", "Urolithiasis, X-Linked Recessive, Type 1", "UROLITHIASIS, X-LINKED RECESSIVE, TYPE 1", "urolithiasis, X-linked recessive, type 1", "nephrolithiasis, type i, X-linked recessive", "nephrolithiasis, X-linked recessive, type 1", "NEPHROLITHIASIS, X-LINKED RECESSIVE, TYPE 1", "Nephrolithiasis, X-Linked Recessive, Type 1", "X-linked recessive nephrolithiasis with renal failure", "Nephrolithiasis, X-Linked Recessive, with Renal Failure", "nephrolithiasis, X-linked recessive, with renal failure", "NEPHROLITHIASIS, X-LINKED RECESSIVE, WITH RENAL FAILURE", "X-linked recessive nephrolithiasis with renal failure (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrolithiasis, X-linked recessive, with renal failure", "shortest_name_length": 3}
{"curie": "UMLS:C0242891", "names": ["Injury;teeth", "teeth injury", "Tooth injury", "Teeth Injury", "TOOTH INJURY", "Tooth Injury", "tooth injury", "Injury, Tooth", "tooth; injury", "Injury, Teeth", "injury; tooth", "tooth injuries", "Tooth Injuries", "Teeth Injuries", "teeth injuries", "injuries teeth", "injury to teeth", "Injuries, Tooth", "Injury of teeth", "Injury to teeth", "Injury of tooth", "Injuries, Teeth", "Tooth injury, NOS", "injuries of tooth", "mouth injury teeth", "Injury of tooth, NOS", "Injury of teeth, NOS", "Injury of teeth (disorder)", "Injury of tooth (disorder)", "Injury of teeth (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tooth Injuries", "shortest_name_length": 12}
{"curie": "MONDO:0021086", "names": ["Gum Tumor", "gum tumor", "gum tumors", "gums tumor", "Gum Neoplasm", "Tumor of Gum", "Tumor of gum", "tumor of gum", "gum neoplasm", "Tumour of gum", "gingiva tumor", "gingival tumor", "Gingival Tumor", "GINGIVAL TUMOR", "Neoplasm of gum", "Neoplasm of Gum", "neoplasm of gum", "gingival tumors", "Tumor of Gingiva", "gingiva neoplasm", "Tumor of gingiva", "tumor of the gum", "tumor of gingiva", "Tumor of the Gum", "Tumour of gingiva", "Gingival Neoplasm", "gingival neoplasm", "Gingival Neoplasms", "Neoplasm, Gingival", "Neoplasm of the Gum", "Neoplasms, Gingival", "Neoplasm of Gingiva", "neoplasm of the gum", "neoplasm of gingiva", "Tumor of the Gingiva", "tumor of the gingiva", "Neoplasm of the Gingiva", "neoplasm of the gingiva", "Neoplasm of gum (disorder)", "gingiva neoplasm (disease)", "neoplasm of gingiva (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gingival neoplasm", "shortest_name_length": 9}
{"curie": "UMLS:C1336434", "names": ["Paranasal Sinus Cancer Stage IV", "Stage IV Paranasal Sinus Cancer", "Stage IV Paranasal Sinus Carcinoma", "Stage IV Accessory Sinus Carcinoma", "Stage IV Carcinoma of Accessory Sinus", "Stage IV Carcinoma of Paranasal Sinus", "Stage IV Paranasal Sinus Cancer AJCC v7", "Stage IV Carcinoma of the Paranasal Sinus", "Stage IV Carcinoma of the Accessory Sinus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Paranasal Sinus Cancer AJCC v7", "shortest_name_length": 31}
{"curie": "MONDO:0007432", "names": ["Casil", "CADASIL", "hereditary multi-infarct dementia", "dementia, hereditary multi-infarct type", "cerebral arteriopathy with subcortical infarcts and leukoencephalopathy", "cerebral arteriopathy with subcortical infaracts and leukoencephalopathy", "cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy", "cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral arteriopathy with subcortical infarcts and leukoencephalopathy", "shortest_name_length": 5}
{"curie": "UMLS:C0006435", "names": ["Caustic burn", "Caustic Burn", "CHEMICAL BURN", "burn chemical", "Chemical Burn", "chemical burn", "Chemical burn", "Chemical Burns", "burns chemical", "chemical burns", "Burn, chemical", "Burn, Chemical", "Chemical burns", "burns chemicals", "Burns, Chemical", "chemical burn(s)", "burning chemicals", "Chemical burn, NOS", "burn from chemicals", "Caustic/Chemical Burns", "Chemical burn (disorder)", "burn from chemicals (diagnosis)", "Chemical burn (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chemical Burns", "shortest_name_length": 12}
{"curie": "MONDO:0041366", "names": ["acute epiglottitis", "Acute epiglottitis", "EPIGLOTTITIS ACUTE", "epiglottitis acute", "EPIGLOTTITIS, ACUTE", "epiglottitis, acute", "Acute epiglottitis (disorder)", "acute epiglottitis (diagnosis)", "Acute epiglottitis and supraglottitis", "acute epiglottitis and supraglottitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute epiglottitis", "shortest_name_length": 18}
{"curie": "MONDO:0019581", "names": ["acral persistent papular mucinosis", "Acral persistent papular mucinosis", "Acral persistent papular mucinosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acral persistent papular mucinosis", "shortest_name_length": 34}
{"curie": "MONDO:0014566", "names": ["CMT2U", "Charcot-Marie-Tooth neuropathy type 2U", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2U", "Charcot-Marie-Tooth neuropathy, type 2U", "MARS Charcot-Marie-Tooth disease type 2", "Charcot-Marie-Tooth disease axonal type 2U", "Charcot-Marie-Tooth disease, axonal, type 2U", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2U", "autosomal dominant Charcot-Marie-Tooth disease type 2U", "Autosomal dominant Charcot-Marie-Tooth disease type 2U", "Charcot-Marie-Tooth disease type 2 caused by mutation in MARS", "autosomal dominant axonal Charcot-Marie-Tooth disease type 2U", "Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2U", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2U", "Autosomal dominant Charcot-Marie-Tooth disease type 2U (disorder)", "Autosomal dominant Charcot-Marie-Tooth disease type 2 due to MARS mutation", "autosomal dominant Charcot-Marie-Tooth disease type 2 due to MARS mutation", "Autosomal dominant Charcot-Marie-Tooth disease type 2 due to MARS (methionyl-tRNA synthetase) mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease axonal type 2U", "shortest_name_length": 5}
{"curie": "MONDO:0002550", "names": ["hypoglossal nerve tumor", "Hypoglossal Nerve Tumor", "Hypoglossal Nerve Tumors", "hypoglossal nerve tumors", "XIIth Cranial Nerve Tumors", "Hypoglossal Nerve Neoplasm", "hypoglossal nerve neoplasm", "tumor of hypoglossal nerve", "tumor of Hypoglossal nerve", "XIIth cranial nerve tumors", "Tumor of Hypoglossal Nerve", "twelfth cranial nerve tumor", "hypoglossal nerve neoplasms", "Hypoglossal Nerve Neoplasms", "Twelfth Cranial Nerve Tumor", "twelfth cranial nerve tumors", "Twelfth Cranial Nerve Tumors", "XIIth Cranial Nerve Neoplasms", "neoplasm of hypoglossal nerve", "Neoplasm of hypoglossal nerve", "Neoplasm of Hypoglossal Nerve", "XIIth cranial nerve neoplasms", "Twelfth Cranial Nerve Neoplasm", "twelfth cranial nerve neoplasm", "Tumor of the Hypoglossal Nerve", "Tumor of Twelfth Cranial Nerve", "tumor of the hypoglossal nerve", "tumor of twelfth cranial nerve", "Twelfth Cranial Nerve Neoplasms", "twelfth cranial nerve neoplasms", "neoplasm of twelfth cranial nerve", "Neoplasm of the Hypoglossal Nerve", "neoplasm of the hypoglossal nerve", "Neoplasm of Twelfth Cranial Nerve", "Tumor of the Twelfth Cranial Nerve", "tumor of the twelfth cranial nerve", "hypoglossal nerve neoplasm (disease)", "Neoplasm of the Twelfth Cranial Nerve", "neoplasm of the twelfth cranial nerve", "Neoplasm of hypoglossal nerve (disorder)", "neoplasm of twelfth cranial nerve (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypoglossal nerve neoplasm", "shortest_name_length": 23}
{"curie": "UMLS:C5668242", "names": ["Unresectable Ovarian Mucinous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Ovarian Mucinous Adenocarcinoma", "shortest_name_length": 44}
{"curie": "MONDO:0011916", "names": ["CMT2K", "Cmt2k", "CMT 2K", "ARCMT2K", "autosomal recessive axonal CMT4C4", "Autosomal recessive axonal CMT4C4", "Charcot-Marie-Tooth disease type 2K", "Charcot-Marie-Tooth Disease Type 2K", "Charcot-Marie-Tooth disease, Type 2K", "Charcot-Marie-Tooth disease axonal type 2K", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K", "Charcot-Marie-Tooth disease, axonal, Type 2K", "Charcot-Marie-Tooth disease, axonal, type 2K", "Charcot-Marie-Tooth neuropathy axonal type 2K", "CHARCOT-MARIE-TOOTH NEUROPATHY, AXONAL, TYPE 2K", "Charcot-Marie-Tooth neuropathy, axonal, type 2K", "Charcot-Marie-Tooth disease type 2K (diagnosis)", "Charcot-Marie-Tooth Neuropathy, Axonal, Type 2k", "Charcot-Marie-Tooth disease, autosomal dominant, type 2K", "Autosomal recessive axonal Charcot-Marie-Tooth disease type 2K", "autosomal recessive axonal Charcot-Marie-Tooth disease type 2K", "Autosomal recessive Charcot-Marie-Tooth disease with hoarseness", "autosomal recessive Charcot-Marie-Tooth disease with hoarseness", "Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2K", "Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2K", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2K", "Charcot-Marie-Tooth disease, axonal, autosomal recessive, Type 2K", "autosomal recessive axonal Charcot-Marie-Tooth disease disease type 2K", "Autosomal recessive Charcot-Marie-Tooth disease with hoarseness (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease axonal type 2K", "shortest_name_length": 5}
{"curie": "MONDO:0010170", "names": ["USH3A", "CLRN1 Usher syndrome", "Usher syndrome type 3A", "Usher syndrome, type 3", "Usher syndrome, type 3A", "Usher syndrome type IIIA", "USHER syndrome, type IIIA", "Usher syndrome caused by mutation in CLRN1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Usher syndrome type 3A", "shortest_name_length": 5}
{"curie": "MONDO:0030005", "names": ["EPEDD", "EPILEPSY, EARLY-ONSET, WITH OR WITHOUT DEVELOPMENTAL DELAY", "epilepsy, early-onset, with or without developmental delay"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, early-onset, with or without developmental delay", "shortest_name_length": 5}
{"curie": "UMLS:C0241075", "names": ["Skin induration", "SKIN INDURATION", "skin induration", "Skin Induration", "skin; induration", "induration; skin", "Induration of skin", "skin induration (diagnosis)", "Induration of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin Induration", "shortest_name_length": 15}
{"curie": "MONDO:0012470", "names": ["HPC7", "PROSTATE CANCER, HEREDITARY, 7", "prostate cancer, hereditary, 7", "PROSTATE CANCER AGGRESSIVENESS", "prostate cancer aggressiveness", "Prostate Cancer, Hereditary, 7", "Prostate Cancer Aggressiveness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate cancer, hereditary, 7", "shortest_name_length": 4}
{"curie": "MONDO:0001034", "names": ["Corneal ulcer marginal", "marginal corneal ulcer", "Marginal corneal ulcer", "Marginal corneal ulcer (disorder)", "marginal corneal ulcer (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "marginal corneal ulcer", "shortest_name_length": 22}
{"curie": "UMLS:C0152002", "names": ["renal angiitis", "ANGITIS KIDNEY", "angiitis kidney", "Renal vasculitis", "renal vasculitis", "vasculitis renal", "RENAL VASCULITIS", "vasculitis kidney", "KIDNEY VASCULITIS", "kidney vasculitis", "Vasculitis kidney", "VASCULITIS KIDNEY", "Kidney vasculitis", "kidney; vasculitis", "kidneys vasculitis", "vasculitis; kidney", "Renal vasculitis, NOS", "Renal vasculitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal vasculitis", "shortest_name_length": 14}
{"curie": "UMLS:C2699200", "names": ["22q Telomere Deletion Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "22q Telomere Deletion Syndrome", "shortest_name_length": 30}
{"curie": "MONDO:0001188", "names": ["esophagus lymphoma", "Esophagus Lymphoma", "oesophagus lymphoma", "esophageal lymphoma", "Esophageal Lymphoma", "Lymphoma of esophagus", "Lymphoma of Esophagus", "lymphoma of esophagus", "Lymphoma of oesophagus", "Lymphoma of the Esophagus", "lymphoma of the esophagus", "primary esophageal lymphoma", "Primary Esophageal Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophagus lymphoma", "shortest_name_length": 18}
{"curie": "MONDO:0001846", "names": ["uterine corpus bizarre leiomyoma", "Uterine Corpus Bizarre Leiomyoma", "body of uterus bizarre leiomyoma", "uterine Corpus Symplastic leiomyoma", "bizarre leiomyoma of body of uterus", "uterine corpus Symplastic leiomyoma", "Uterine Corpus Symplastic Leiomyoma", "uterine corpus leiomyoma, atypical variant", "Uterine Corpus Leiomyoma, Atypical Variant", "uterine corpus leiomyoma with bizarre nuclei", "Uterine Corpus Leiomyoma with Bizarre Nuclei"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine corpus bizarre leiomyoma", "shortest_name_length": 32}
{"curie": "MONDO:0003060", "names": ["biliary cancer", "biliary cancers", "biliary tree cancer", "Biliary Tract Cancer", "biliary tract cancer", "Biliary Tract Cancers", "Biliary tract--Cancer", "Cancer, Biliary Tract", "biliary cancers tract", "cancer of biliary tree", "Cancers, Biliary Tract", "Cancer of Biliary Tract", "cancer of biliary tract", "Cancer of the Biliary Tract", "malignant biliary tree neoplasm", "Malignant tumor of biliary tract", "malignant tumor of biliary tract", "Malignant tumour of biliary tract", "malignant tumour of biliary tract", "malignant neoplasm of biliary tree", "malignant neoplasm of biliary tract", "Malignant neoplasm of biliary tract, NOS", "Malignant tumor of biliary tract (disorder)", "malignant neoplasm of biliary tract (diagnosis)", "Malignant neoplasm of biliary tract, unspecified", "Malignant neoplasm of biliary tract, part unspecified", "Malignant neoplasm of biliary tract, part unspecified site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "biliary tract cancer", "shortest_name_length": 14}
{"curie": "MONDO:0024546", "names": ["COA", "CIO", "PHOAR1", "Currarino disease", "Cranioosteoarthropathy", "CRANIOOSTEOARTHROPATHY", "Cranio-osteoarthropathy", "Cranioosteoarthropathies", "Pho, autosomal recessive", "PDP, autosomal recessive", "Touraine-Solente-Gole syndrome", "Reginato-Schiapachasse syndrome", "Cranioosteoarthropathy (disorder)", "CURRARINO IDIOPATHIC OSTEOARTHROPATHY", "Currarino idiopathic osteoarthropathy", "Currarino Idiopathic Osteoarthropathy", "Osteoarthropathy, Currarino Idiopathic", "pachydermoperiostosis, autosomal recessive", "HPGD primary hypertrophic osteoarthropathy", "FAMILIAL IDIOPATHIC OSTEOARTHROPATHY OF CHILDHOOD", "familial idiopathic osteoarthropathy of childhood", "Familial Idiopathic Osteoarthropathy Of Childhood", "hypertrophic osteoarthropathy, primary, autosomal recessive 1", "hypertrophic osteoarthropathy, primary, autosomal recessive, 1", "HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1", "primary hypertrophic osteoarthropathy caused by mutation in HPGD", "Primary Hypertrophic Osteoarthropathy, Autosomal Recessive Type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophic osteoarthropathy, primary, autosomal recessive, 1", "shortest_name_length": 3}
{"curie": "UMLS:C1336402", "names": ["Stage IVC Mouth Carcinoma", "Stage IVC Carcinoma of Mouth", "Stage IVC Oral Cavity Cancer", "Stage IVC Oral Cavity Carcinoma", "Stage IVC Carcinoma of the Mouth", "Stage IVC Carcinoma of Oral Cavity", "Stage IVC Oral Cavity Cancer AJCC v6", "Stage IVC Oral Cavity Cancer AJCC v7", "Stage IVC Carcinoma of the Oral Cavity", "Stage IVC Oral Cavity Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Oral Cavity Cancer AJCC v6 and v7", "shortest_name_length": 25}
{"curie": "MONDO:0020767", "names": ["bladder; neurogenic, cauda equina syndrome", "neurogenic; bladder, cauda equina syndrome", "Cauda Equina Syndrome with Neurogenic Bladder", "cauda equina syndrome with neurogenic bladder", "Cauda equina syndrome with neurogenic bladder", "cauda equina syndrome with acontractile bladder", "Cauda equina syndrome with neurogenic bladder (disorder)", "cauda equina syndrome with neurogenic bladder (diagnosis)", "cauda equina syndrome with acontractile bladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cauda equina syndrome with neurogenic bladder", "shortest_name_length": 42}
{"curie": "MONDO:0003780", "names": ["T-cell immunodeficiency", "T lymphocyte deficiency", "T-Cell Immunodeficiency", "T-lymphocyte immunodeficiency", "T-lymphocyte deficiency (finding)", "T-lymphocyte immunodeficiency (disorder)", "T-lymphocyte immunodeficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-cell immunodeficiency", "shortest_name_length": 23}
{"curie": "UMLS:C1708777", "names": ["Lung Mucinous Cystadenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Mucinous Cystadenoma", "shortest_name_length": 25}
{"curie": "MONDO:0015826", "names": ["Autosomal dominant spondylocostal dysplasia", "autosomal dominant spondylocostal dysplasia", "Autosomal dominant spondylocostal dysostosis", "autosomal dominant spondylocostal dysostosis", "spondylocostal dysostosis, autosomal dominant", "Autosomal dominant spondylocostal dysostosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant spondylocostal dysostosis", "shortest_name_length": 43}
{"curie": "UMLS:C4724965", "names": ["Refractory Leiomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Leiomyosarcoma", "shortest_name_length": 25}
{"curie": "MONDO:0013633", "names": ["IIAE4", "CPT2 encephalopathy, acute, infection-induced", "encephalopathy, acute, infection-induced, susceptibility to, 4", "encephalopathy, acute, infection-induced, 4, susceptibility to", "ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 4", "encephalopathy, acute, infection-induced caused by mutation in CPT2", "encephalopathy, acute, infection-induced, susceptibility to, type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephalopathy, acute, infection-induced, susceptibility to, 4", "shortest_name_length": 5}
{"curie": "MONDO:0012214", "names": ["FGD3", "GCCD3", "GCCD2, FORMERLY", "Glucocorticoid Deficiency 3", "glucocorticoid deficiency 3", "glucocorticoid deficiency 2", "GLUCOCORTICOID DEFICIENCY 3", "Non-classic CLAH (FGD variant)", "familial glucocorticoid deficiency 3", "FAMILIAL GLUCOCORTICOID DEFICIENCY 3", "Familial Glucocorticoid Deficiency 3", "GLUCOCORTICOID DEFICIENCY 2, FORMERLY", "glucocorticoid deficiency 2, formerly", "GLUCOCORTICOID DEFICIENCY 3 (disorder)", "Familial Glucocorticoid Deficiency Type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glucocorticoid deficiency 3", "shortest_name_length": 4}
{"curie": "UMLS:C0854827", "names": ["Refractory T-Cell Lymphoma", "T-Cell Lymphoma Refractory", "T-cell lymphoma refractory", "T-cell lymphoma NOS refractory", "Refractory T-Cell Non-Hodgkin Lymphoma", "Refractory T-Cell Non-Hodgkin's Lymphoma", "Refractory T-Cell and NK-Cell Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-cell lymphoma refractory", "shortest_name_length": 26}
{"curie": "UMLS:C0920701", "names": ["Environment-Related Neoplasm", "environment related neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Environment-Related Neoplasm", "shortest_name_length": 28}
{"curie": "UMLS:C3897523", "names": ["Stage IVA Lip and Oral Cavity Squamous Cell Cancer", "Stage IVA Lip and Oral Cavity Squamous Cell Carcinoma", "Stage IVA Lip and Oral Cavity Squamous Cell Carcinoma AJCC v7", "Stage IVA Lip and Oral Cavity Squamous Cell Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Lip and Oral Cavity Squamous Cell Carcinoma AJCC v6 and v7", "shortest_name_length": 50}
{"curie": "UMLS:C1699325", "names": ["Urostomy perforation", "Urostomy Perforation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urostomy perforation", "shortest_name_length": 20}
{"curie": "MONDO:0010848", "names": ["SCA5", "Spinocerebellar Ataxia 5", "SPINOCEREBELLAR ATAXIA 5", "spinocerebellar ataxia 5", "Spinocerebellar Ataxia-5", "Ataxia 5, Spinocerebellar", "Spinocerebellar Ataxia 5s", "Spinocerebellar Ataxia Type 5", "Type 5 Spinocerebellar Ataxia", "Spinocerebellar ataxia type 5", "spinocerebellar ataxia type 5", "Spinocerebellar ataxia type 5 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia type 5", "shortest_name_length": 4}
{"curie": "MONDO:0045020", "names": ["glycine metabolism disease", "metabolic disorder; glycine", "glycine; metabolic disorder", "disorder of glycine metabolism", "Disorder of glycine metabolism", "DISORDERS OF GLYCINE METABOLISM", "glycine metabolism disturbances", "Disorders of glycine metabolism", "glycine metabolic process disease", "Disorder of glycine metabolism, NOS", "disorder of glycine metabolic process", "Disorder of glycine metabolism (disorder)", "glycine metabolism disturbances (diagnosis)", "Disorder of glycine metabolism, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycine metabolism disease", "shortest_name_length": 26}
{"curie": "UMLS:C2827980", "names": ["Stage IA Breast Cancer", "stage IA breast cancer", "Stage IA Breast Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Breast Cancer AJCC v7", "shortest_name_length": 22}
{"curie": "UMLS:C4527063", "names": ["Clinical Stage IV Merkel Cell Carcinoma AJCC v8", "Clinical Stage IV Neuroendocrine Carcinoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage IV Merkel Cell Carcinoma AJCC v8", "shortest_name_length": 47}
{"curie": "UMLS:C5554614", "names": ["Microsatellite Stable Colon Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Microsatellite Stable Colon Carcinoma", "shortest_name_length": 37}
{"curie": "UMLS:C0855140", "names": ["Relapsed Nodal Marginal Zone Lymphoma", "Recurrent Nodal Marginal Zone Lymphoma", "Nodal marginal zone B-cell lymphoma recurrent", "Recurrent Nodal Marginal Zone B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nodal marginal zone B-cell lymphoma recurrent", "shortest_name_length": 37}
{"curie": "MONDO:0000554", "names": ["UEA", "adenocarcinoma endocervix", "endocervix adenocarcinoma", "endocervical adenocarcinoma", "Endocervical adenocarcinoma", "adenocarcinoma of endocervix", "Adenocarcinoma of endocervix", "Adenocarcinoma, Endocervical Type", "Adenocarcinoma, endocervical type", "Cervical Adenocarcinoma, Usual Type", "Cervical Adenocarcinoma, Usual-Type", "endocervical adenocarcinoma of cervix", "Endocervical adenocarcinoma usual type", "Endocervical adenocarcinoma (disorder)", "Endocervical Adenocarcinoma, Usual Type", "Endocervical Adenocarcinoma, Usual-Type", "endocervical adenocarcinoma, usual type", "Mucinous adenocarcinoma, endocervical type", "endocervical adenocarcinoma of cervix (diagnosis)", "Cervical Mucinous Adenocarcinoma, Endocervical-Type", "Cervical Mucinous Adenocarcinoma, Endocervical Type", "Adenocarcinoma, endocervical type (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endocervical adenocarcinoma", "shortest_name_length": 3}
{"curie": "MONDO:0041806", "names": ["Drug-Resistant Tuberculosis", "drug-resistant tuberculosis", "drug resistant tuberculosis", "tuberculosis drug resistant", "Drug resistant tuberculosis", "Tuberculosis, Drug-Resistant", "Tuberculosis, Drug Resistant", "Drug resistant tuberculosis (disorder)", "drug-resistant tuberculosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "drug-resistant tuberculosis", "shortest_name_length": 27}
{"curie": "UMLS:C0272694", "names": ["Finger fracture", "fracture finger", "finger fracture", "FINGER FRACTURE", "Finger Fracture", "fractured finger", "Fractured finger", "fingers fracture", "finger fractures", "fracture fingers", "fracture; finger", "fingers fractured", "Fracture;finger(s)", "Fracture of finger", "finger(s); fracture", "phalanx fracture hand", "fracture phalanx hand", "Phalanx (Hand) Fracture", "fracture; hand, phalanx", "hand; fracture, phalanx", "Fracture of finger, NOS", "phalanx; fracture finger", "fracture; phalanx fingers", "phalanx fracture of finger", "Fracture of phalanx of hand", "fracture of phalanges of hand", "fracture of phalanx of finger", "Fracture of phalanx of finger", "fracture of phalanges of finger", "Fracture of phalanx of finger, NOS", "Fracture of phalanx of hand (disorder)", "Fracture of phalanx of finger (disorder)", "fracture of phalanges of hand (diagnosis)", "fracture of phalanx of finger (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fracture of phalanx of finger", "shortest_name_length": 15}
{"curie": "MONDO:0000724", "names": ["Dysphasia", "specific language disorder", "Specific Language Disorder", "Specific language disorder", "Disorder, Specific Language", "Specific Language Disorders", "Language Disorder, Specific", "Language Disorders, Specific", "Specific language impairment", "Disorders, Specific Language", "Specific Language Impairment", "specific language impairment", "Impairment, Specific Language", "Language Impairment, Specific", "language impairment (disease)", "Specific Language Impairments", "impairments language specific", "Impairments, Specific Language", "Language Impairments, Specific", "Specific language impairment (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "specific language impairment", "shortest_name_length": 9}
{"curie": "MONDO:0000749", "names": ["abscess breast", "Abscess breast", "BREAST ABSCESS", "Breast abscess", "breast abscess", "ABSCESS BREAST", "breast; abscess", "BREAST, ABSCESS", "abscess; breast", "MAMMARY ABSCESS", "abscesses breast", "Abscess of breast", "Mammary gland abscess", "Abscess of breast, NOS", "Abscess of breast (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast abscess", "shortest_name_length": 14}
{"curie": "MONDO:0700027", "names": ["chromosome X disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome X disorder", "shortest_name_length": 21}
{"curie": "MONDO:0009178", "names": ["EBR3", "EBR 3", "Goldscheider", "Goldscheider disease", "Goldscheider's disease", "epidermolysis bullosa progressiva, recessive", "Epidermolysis Bullosa Progressiva, Recessive", "EPIDERMOLYSIS BULLOSA PROGRESSIVA, RECESSIVE", "EPIDERMOLYSIS BULLOSA WITH CONGENITAL DEAFNESS", "epidermolysis bullosa with congenital deafness", "Epidermolysis Bullosa With Congenital Deafness", "epidermolysis bullosa dystrophica Neurotrophica", "Epidermolysis Bullosa Dystrophica Neurotrophica", "Epidermolysis bullosa dystrophica neurotrophica", "EPIDERMOLYSIS BULLOSA DYSTROPHICA NEUROTROPHICA", "Progressive recessive dystrophic epidermolysis bullosa", "Epidermolysis bullosa progressiva with congenital deafness", "Progressive recessive dystrophic epidermolysis bullosa (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolysis bullosa dystrophica Neurotrophica", "shortest_name_length": 4}
{"curie": "MONDO:0019815", "names": ["accessory tricuspid valve tissue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "accessory tricuspid valve tissue", "shortest_name_length": 32}
{"curie": "MONDO:0032567", "names": ["IGHD4", "IGHD1B, FORMERLY", "Dwarfism of Sindh", "DWARFISM OF SINDH", "isolated growth hormone deficiency, type 4", "ISOLATED GROWTH HORMONE DEFICIENCY, TYPE IV", "Isolated Growth Hormone Deficiency, Type Ib", "growth hormone deficiency, isolated, type IV", "ISOLATED GROWTH HORMONE DEFICIENCY, TYPE IB, FORMERLY", "Isolated Growth Hormone Deficiency, Type Ib, Formerly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated growth hormone deficiency, type 4", "shortest_name_length": 5}
{"curie": "MONDO:0019821", "names": ["aneurysm or dilatation of ascending aorta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aneurysm or dilatation of ascending aorta", "shortest_name_length": 41}
{"curie": "MONDO:0020426", "names": ["malposition of the coronary ostium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malposition of the coronary ostium", "shortest_name_length": 34}
{"curie": "UMLS:C2987516", "names": ["CIN 3", "CIN Grade 3", "CIN 3 AJCC v7", "CIN Grade 3 AJCC v7", "Stage 0 Cervical Cancer", "Severe Cervical Dysplasia", "Cervical Carcinoma in situ", "Carcinoma in situ of the Cervix", "Stage 0 Cervical Cancer AJCC v7", "Severe Cervical Dysplasia AJCC v7", "Severe Dysplasia of Uterine Cervix", "stage 0 cervical carcinoma in situ", "Cervical Carcinoma in situ AJCC v7", "Carcinoma in situ of the Cervix AJCC v7", "Cervix Intraepithelial Neoplasia Grade 3", "Severe Dysplasia of Uterine Cervix AJCC v7", "Cervix Intraepithelial Neoplasia Grade 3 AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervix Intraepithelial Neoplasia Grade 3 AJCC v7", "shortest_name_length": 5}
{"curie": "UMLS:C4521966", "names": ["Stage I Lung Cancer", "Stage I Lung Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Lung Cancer AJCC v7", "shortest_name_length": 19}
{"curie": "UMLS:C4761423", "names": ["HBC", "Histiocytoid Breast Carcinoma", "Breast Histiocytoid Carcinoma", "Histiocytoid Lobular Breast Carcinoma", "Invasive Histiocytoid Breast Carcinoma", "Infiltrating Histiocytoid Breast Carcinoma", "Invasive Histiocytoid Lobular Breast Carcinoma", "Infiltrating Histiocytoid Lobular Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Histiocytoid Breast Carcinoma", "shortest_name_length": 3}
{"curie": "MONDO:0003358", "names": ["anus leiomyosarcoma", "Anal Leiomyosarcoma", "anal leiomyosarcoma", "leiomyosarcoma of anus", "Leiomyosarcoma of Anus", "Leiomyosarcoma of the Anus", "leiomyosarcoma of the anus", "leiomyosarcoma of anus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anus leiomyosarcoma", "shortest_name_length": 19}
{"curie": "MONDO:0017411", "names": ["neonatal inflammatory skin and bowel disease", "inflammatory skin and bowel disease, neonatal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal inflammatory skin and bowel disease", "shortest_name_length": 44}
{"curie": "MONDO:0017852", "names": ["Tsao-Ellingson syndrome", "Tsao Ellingson syndrome", "infantile spasms broad thumbs", "infantile spasms-broad thumbs syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile spasms-broad thumbs syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0024773", "names": ["SPGFX4", "SPERMATOGENIC FAILURE, X-LINKED, 4", "spermatogenic failure, X-linked, 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure, X-linked, 4", "shortest_name_length": 6}
{"curie": "UMLS:C0233720", "names": ["Poverty of speech", "Speech Poverty Of Content", "Poverty of speech (finding)", "Poverty of content of speech"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Poverty of speech", "shortest_name_length": 17}
{"curie": "MONDO:0011779", "names": ["Lel", "LEL", "LARYNGEAL ATRESIA, ENCEPHALOCELE, AND LIMB DEFORMITIES", "laryngeal atresia, encephalocele, and limb deformities", "Laryngeal Atresia, Encephalocele, and Limb Deformities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laryngeal atresia, encephalocele, and limb deformities", "shortest_name_length": 3}
{"curie": "UMLS:C2363914", "names": ["Post procedural constipation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post procedural constipation", "shortest_name_length": 28}
{"curie": "UMLS:C4525737", "names": ["Stage IIA Colorectal Neuroendocrine Tumor", "Stage IIA Colorectal Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Colorectal Neuroendocrine Tumor AJCC v8", "shortest_name_length": 41}
{"curie": "UMLS:C5447371", "names": ["Locally Recurrent Head and Neck Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Recurrent Head and Neck Squamous Cell Carcinoma", "shortest_name_length": 55}
{"curie": "UMLS:C0264313", "names": ["Keratotic Vocal Cord", "Keratotic vocal cord", "Leucoplakia of glottis", "Vocal Cord Leukoplakia", "cord leukoplakia vocal", "vocal cord leukoplakia", "Vocal cord leukoplakia", "Leukoplakia of glottis", "Vocal cord leucoplakia", "leukoplakia; vocal cord", "vocal cord; leukoplakia", "leukoplakia of vocal cord", "Leukoplakia of vocal cords", "leukoplakia of vocal cords", "Leucoplakia of vocal cords", "Leukoplakia of Vocal Cords", "vocal cord; leukokeratosis", "leukokeratosis; vocal cord", "Leukokeratosis of vocal cords", "Leukoplakia of vocal cords (disorder)", "leukoplakia of vocal cord (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leukoplakia of vocal cords", "shortest_name_length": 20}
{"curie": "UMLS:C4520723", "names": ["Stage II Soft Tissue Sarcoma", "stage II adult soft tissue sarcoma", "Stage II Adult Sarcoma of Soft Tissue", "Stage II Adult Sarcoma of the Soft Tissue", "Stage II Adult Soft Tissue Sarcoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Adult Soft Tissue Sarcoma AJCC v7", "shortest_name_length": 28}
{"curie": "MONDO:0012405", "names": ["HMPS2", "hereditary mixed polyposis syndrome 2", "polyposis syndrome, hereditary mixed, 2", "POLYPOSIS SYNDROME, HEREDITARY MIXED, 2", "Polyposis Syndrome, Hereditary Mixed, 2", "BMPR1A hereditary mixed polyposis syndrome", "polyposis syndrome, hereditary mixed, type 2", "hereditary mixed polyposis syndrome caused by mutation in BMPR1A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyposis syndrome, hereditary mixed, 2", "shortest_name_length": 5}
{"curie": "MONDO:0030894", "names": ["AMEDS", "AMED syndrome", "AMeD syndrome", "AMED syndrome, digenic", "bone marrow failure syndrome 7, digenic", "aplastic anemia-intellectual disability-dwarfism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AMED syndrome, digenic", "shortest_name_length": 5}
{"curie": "UMLS:C4683601", "names": ["Lugano Classification Advanced Stage Childhood Hodgkin Lymphoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lugano Classification Advanced Stage Childhood Hodgkin Lymphoma AJCC v8", "shortest_name_length": 71}
{"curie": "MONDO:0800044", "names": ["CDDG", "CDDG1", "CDG1V", "CDG IV", "NGLY1-CDDG", "CDG1V, FORMERLY", "CDG IV, formerly", "NGLY1 deficiency", "NGLY1-deficiency", "Deficiency of N-glycanase 1", "deficiency of N-glycanase 1", "congenital disorder of deglycosylation", "CONGENITAL DISORDER OF DEGLYCOSYLATION", "Congenital Disorder of Deglycosylation", "Congenital disorder of deglycosylation", "congenital disorder of deglycosylation 1", "CONGENITAL DISORDER OF DEGLYCOSYLATION 1", "congenital disorder of deglycosylation;CDDG", "NGLY1-congenital disorder of deglycosylation", "congenital disorder of glycosylation type Iv", "congenital disorder of glycosylation type IV", "Congenital disorder of glycosylation, type Iv", "congenital disorder of glycosylation, type IV", "N-glycanase 1 congenital disorder of deglycosylation", "Alacrimia-choreoathetosis-liver dysfunction syndrome", "Alacrimia, choreoathetosis, liver dysfunction syndrome", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv, FORMERLY", "congenital disorder of glycosylation, type IV, formerly", "alacrimia - choreoathetosis - liver dysfunction syndrome", "N-glycanase 1 congenital disorder of deglycosylation (disorder)", "N-glycanase 1 congenital disorder of deglycosylation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital disorder of deglycosylation 1", "shortest_name_length": 4}
{"curie": "UMLS:C0751334", "names": ["Progressive Proximal Myelopathic Muscular Atrophy", "Proximal Myelopathic Muscular Atrophy, Progressive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Progressive Proximal Myelopathic Muscular Atrophy", "shortest_name_length": 49}
{"curie": "UMLS:C4553673", "names": ["Stage IIIA Penile Cancer", "Stage IIIA Penile Cancer AJCC v8", "Stage IIIA Penile Squamous Cell Carcinoma AJCC v8", "Stage IIIA Squamous Cell Carcinoma of the Penis AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Penile Cancer AJCC v8", "shortest_name_length": 24}
{"curie": "UMLS:C1336417", "names": ["Extrahepatic Bile Duct Cancer Stage IV", "stage IV extrahepatic bile duct cancer", "Stage IV Extrahepatic Bile Duct Cancer", "Stage IV Extrahepatic Bile Duct Carcinoma", "Stage IV Carcinoma of Extrahepatic Bile Duct", "Stage IV Carcinoma of the Extrahepatic Bile Duct"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Extrahepatic Bile Duct Cancer", "shortest_name_length": 38}
{"curie": "UMLS:C0333450", "names": ["Mucous degeneration", "Mucinous Degeneration", "Mucinous degeneration", "Mucinous degeneration (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mucinous degeneration", "shortest_name_length": 19}
{"curie": "MONDO:0009536", "names": ["LYMPHOBLASTIC TRANSFORMATION, INTRINSIC DEFECT IN", "lymphoblastic transformation, intrinsic defect IN", "Lymphoblastic Transformation, Intrinsic Defect in", "lymphoblastic transformation, intrinsic defect type 1N", "chronic mucocutaneous candidiasis due to intrinsic defect in lymphoblastic transformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic mucocutaneous candidiasis due to intrinsic defect in lymphoblastic transformation", "shortest_name_length": 49}
{"curie": "MONDO:0007470", "names": ["CDL", "CDLSMD", "Familial doughnut lesions of skull", "familial doughnut lesions of skull", "doughnut lesions of skull, familial", "Doughnut Lesions of Skull, Familial", "DOUGHNUT LESIONS OF SKULL, FAMILIAL", "calvarial doughnut lesions with bone fragility", "CALVARIAL DOUGHNUT LESIONS WITH BONE FRAGILITY", "calvarial doughnut lesions-bone fragility syndrome", "Calvarial doughnut lesions-bone fragility syndrome", "Calvarial doughnut lesion with bone fragility syndrome", "Doughnut lesion of calvaria and bone fragility syndrome", "Doughnut lesion of calvaria and bone fragility syndrome (disorder)", "CALVARIAL DOUGHNUT LESIONS WITH BONE FRAGILITY AND SPONDYLOMETAPHYSEAL DYSPLASIA", "calvarial doughnut lesions with bone fragility with or without spondylometaphyseal dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "calvarial doughnut lesions-bone fragility syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C1536010", "names": ["Lymphoma transformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoma transformation", "shortest_name_length": 23}
{"curie": "MONDO:0034670", "names": ["non-syndromic postaxial polydactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-syndromic postaxial polydactyly", "shortest_name_length": 35}
{"curie": "MONDO:0006482", "names": ["ureter small cell carcinoma", "Ureter Small Cell Carcinoma", "ureteral small cell carcinoma", "Ureteral Small Cell Carcinoma", "small cell carcinoma of ureter", "Small Cell Carcinoma of Ureter", "small cell carcinoma of the ureter", "Small Cell Carcinoma of the Ureter", "small cell carcinoma of ureter (diagnosis)", "Ureter Small Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ureter small cell carcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0013428", "names": ["MGORS2", "Meier-Gorlin syndrome 2", "MEIER-GORLIN SYNDROME 2", "Meier-GORLIN syndrome 2", "ORC4 Meier-Gorlin syndrome", "Meier-Gorlin syndrome type 2", "Meier-Gorlin syndrome caused by mutation in ORC4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meier-Gorlin syndrome 2", "shortest_name_length": 6}
{"curie": "MONDO:0008467", "names": ["Czeizel Losonci syndrome", "Czeizel-Losonci syndrome", "split hand urinary anomalies spina bifida", "split hand-urinary anomalies-spina bifida syndrome", "Split hand-urinary anomalies-spina bifida syndrome", "Split hand, urinary anomalies, spina bifida syndrome", "Split hand with obstructive uropathy, spina bifida and diaphragmatic defects", "split hand with obstructive uropathy, spina bifida and diaphragmatic defects", "SPLIT-HAND WITH OBSTRUCTIVE UROPATHY, SPINA BIFIDA, AND DIAPHRAGMATIC DEFECTS", "split-hand with obstructive uropathy, spina bifida, and diaphragmatic defects", "Split-Hand With Obstructive Uropathy, Spina Bifida, And Diaphragmatic Defects", "Split hand, obstructive uropathy, spina bifida, diaphragmatic defect syndrome", "Split hand, obstructive uropathy, spina bifida, diaphragmatic defect syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Czeizel-Losonci syndrome", "shortest_name_length": 24}
{"curie": "UMLS:C3272779", "names": ["Appendix Neuroma", "Neurogenic Appendicopathy", "Appendix Fibrous Obliteration", "Appendix Neurogenous Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Appendix Neuroma", "shortest_name_length": 16}
{"curie": "UMLS:C0278724", "names": ["stage III multiple myeloma", "Stage III Multiple Myeloma", "Multiple Myeloma Stage III", "multiple myeloma, stage III", "DS Stage III Multiple Myeloma", "Stage III Plasma Cell Myeloma", "plasma cell neoplasm, stage III", "DS Stage III Plasma Cell Myeloma", "Durie/Salmon Stage III Multiple Myeloma", "Durie/Salmon Stage III Plasma Cell Myeloma", "DS Stage III Multiple Myeloma/Plasma Cell Myeloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DS Stage III Plasma Cell Myeloma", "shortest_name_length": 26}
{"curie": "UMLS:C1524056", "names": ["Breast Adenolipoma", "BREAST, ADENOLIPOMA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Adenolipoma", "shortest_name_length": 18}
{"curie": "MONDO:0012601", "names": ["AUTS10", "AUTISM, SUSCEPTIBILITY TO, 10", "autism, susceptibility to, 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autism, susceptibility to, 10", "shortest_name_length": 6}
{"curie": "MONDO:0024458", "names": ["visual system disease", "visual system disorder", "disease of visual system", "disorder of visual system", "visual system disease or disorder", "disease or disorder of visual system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of visual system", "shortest_name_length": 21}
{"curie": "UMLS:C0854966", "names": ["Stage II Penile Cancer", "stage II penile cancer", "penis cancer, stage II", "penile cancer, stage II", "Penis carcinoma stage II", "Stage II Carcinoma of Penis", "Stage II Penile Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Carcinoma of Penis", "shortest_name_length": 22}
{"curie": "UMLS:C0457193", "names": ["SOFT TISSUE MASS", "soft tissue mass", "Soft tissue mass", "masses soft tissue", "Mass of soft tissue", "Mass of soft tissue (finding)", "Soft tissue mass (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mass of soft tissue", "shortest_name_length": 16}
{"curie": "UMLS:C1708272", "names": ["HIV Lipodystrophy", "HIV-Lipodystrophy", "HIV lipodystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HIV lipodystrophy", "shortest_name_length": 17}
{"curie": "OMIM:607486", "names": [], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"]}
{"curie": "UMLS:C5555173", "names": ["Refractory Fallopian Tube Mucinous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Fallopian Tube Mucinous Adenocarcinoma", "shortest_name_length": 49}
{"curie": "MONDO:0000160", "names": ["FAME", "BAFME", "FCMTE", "familial adult myoclonic epilepsy", "epilepsy, familial adult myoclonic", "benign adult familial myoclonus epilepsy", "benign adult familial myoclonic epilepsy", "familial cortical myoclonic tremor and epilepsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, familial adult myoclonic", "shortest_name_length": 4}
{"curie": "MONDO:0003351", "names": ["colon leiomyosarcoma", "Colon Leiomyosarcoma", "Colonic leiomyosarcoma", "colonic leiomyosarcoma", "Colonic Leiomyosarcoma", "Leiomyosarcoma of Colon", "leiomyosarcoma of colon", "Leiomyosarcoma of colon", "leiomyosarcoma of the colon", "Leiomyosarcoma of the Colon", "Leiomyosarcoma of colon (disorder)", "leiomyosarcoma of colon (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colon leiomyosarcoma", "shortest_name_length": 20}
{"curie": "UMLS:C1334206", "names": ["DIN 2", "DCIS Grade 2", "Intermediate-Grade DCIS", "Ductal Intraepithelial Neoplasia, Grade 2", "Intermediate Grade Ductal Breast Carcinoma In Situ", "Breast Ductal Carcinoma In Situ, Intermediate Grade", "Intermediate-Grade Ductal Carcinoma In Situ of Breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Ductal Carcinoma In Situ, Intermediate Grade", "shortest_name_length": 5}
{"curie": "UMLS:C1535882", "names": ["Lower respiratory tract infection bacterial", "bacterial lower respiratory tract infection", "Bacterial lower respiratory tract infections", "infection of lower respiratory tract bacterial", "bacterial lower respiratory tract infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lower respiratory tract infection bacterial", "shortest_name_length": 43}
{"curie": "UMLS:C1336429", "names": ["Stage IV Mouth Carcinoma", "Stage IV Oral Cavity Cancer", "Stage IV Carcinoma of Mouth", "Stage IV Oral Cavity Carcinoma", "Stage IV Carcinoma of the Mouth", "Stage IV Carcinoma of Oral Cavity", "Stage IV Oral Cavity Cancer AJCC v6", "Stage IV Oral Cavity Cancer AJCC v7", "Stage IV Carcinoma of the Oral Cavity", "Stage IV Oral Cavity Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Oral Cavity Cancer AJCC v6 and v7", "shortest_name_length": 24}
{"curie": "UMLS:C3897516", "names": ["Stage IVB Lip and Oral Cavity Squamous Cell Cancer", "Stage IVB Lip and Oral Cavity Squamous Cell Carcinoma", "Stage IVB Lip and Oral Cavity Squamous Cell Carcinoma AJCC v7", "Stage IVB Lip and Oral Cavity Squamous Cell Carcinoma AJCC v6", "Stage IVB Lip and Oral Cavity Squamous Cell Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Lip and Oral Cavity Squamous Cell Carcinoma AJCC v6 and v7", "shortest_name_length": 50}
{"curie": "MONDO:0019266", "names": ["PPHS", "SAPHO Syndrome", "sapho syndrome", "SAPHO syndrome", "Syndrome, SAPHO", "SAPHO Syndromes", "Syndromes, SAPHO", "acquired hyperostosis syndrome", "Acquired Hyperostosis Syndrome", "Acquired Hyperostosis Syndromes", "Hyperostosis Syndrome, Acquired", "Syndrome, Acquired Hyperostosis", "Syndromes, Acquired Hyperostosis", "Hyperostosis Syndromes, Acquired", "synovitis acne pustulosis hyperostosis osteitis", "Pustulo-psoriatic hyperostotic Spondyloarthritis", "Pustulo-Psoriatic Hyperostotic Spondyloarthritis", "synovitis-acne-pustulosis-hyperostosis-osteitis syndrome", "Synovitis-acne-pustulosis-hyperostosis-osteitis syndrome", "Synovitis, Acne, Pustlosis, Hyperostosis, and Osteomyelitis", "synovitis, acne, Pustlosis, hyperostosis, and osteomyelitis", "synovitis acne pustulosis hyperostosis osteomyelitis syndrome", "Synovitis acne pustulosis hyperostosis osteomyelitis syndrome", "Synovitis, Acne, Pustulosis, Hyperostosis, and Osteitis Syndrome", "synovitis, acne, pustulosis, hyperostosis, and osteitis syndrome", "Synovitis acne pustulosis hyperostosis osteomyelitis syndrome (disorder)", "synovitis acne pustulosis hyperostosis osteomyelitis syndrome (diagnosis)", "synovitis, acne, pustulosis palmaris, hyperostosis, osteomyelitis syndrome", "Synovitis, acne, pustulosis palmaris, hyperostosis, osteomyelitis syndrome", "SAPHO - Synovitis, acne, pustulosis palmaris, hyperostosis, osteomyelitis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SAPHO syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0019645", "names": ["bilateral renal dysplasia", "Bilateral renal dysplasia", "Bilateral Renal Dysplasia", "Bilateral renal dysgenesis", "Renal dysplasia, bilateral", "renal dysplasia, bilateral", "Kidney dysplasia, bilateral", "dysgenesis; kidney, bilateral", "renal dysplasia of both kidneys", "Bilateral renal dysplasia (disorder)", "renal dysplasia of both kidneys (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal dysplasia, bilateral", "shortest_name_length": 25}
{"curie": "UMLS:C4553239", "names": ["Stage II Prostate Cancer", "Stage II Prostate Cancer AJCC v8", "Stage II Prostate Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Prostate Cancer AJCC v8", "shortest_name_length": 24}
{"curie": "UMLS:C0433445", "names": ["Third-Degree Burn", "Third Degree Burn", "THIRD DEGREE BURN", "Third degree burn", "third degree burn", "burn degree third", "burns degree third", "Third degree burns", "third degree burns", "Burns third degree", "Full thickness burn", "full thickness burn", "burns full thickness", "FT - Full thickness burn", "Third degree burn injury", "third degree burns (diagnosis)", "Full thickness burn (disorder)", "Burn with full-thickness skin loss", "Full thickness (Third Degree) Burn", "full thickness (third degree) burns", "Third degree burn injury (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Full thickness burn", "shortest_name_length": 17}
{"curie": "MONDO:0030361", "names": ["AGS8", "AICARDI-GOUTIERES SYNDROME 8", "Aicardi-Goutieres syndrome 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aicardi-Goutieres syndrome 8", "shortest_name_length": 4}
{"curie": "UMLS:C1336920", "names": ["Uterine Non-Neoplastic Disease", "Uterine Non-Neoplastic Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Non-Neoplastic Disorder", "shortest_name_length": 30}
{"curie": "MONDO:0019904", "names": ["R3", "Ring 3", "ROSE Cluster 3", "rose cluster 3", "Ring chromosome 3", "ring chromosome 3", "chromosome 3 ring", "Ring chromosome type 3", "Ring chromosome 3 syndrome", "Ring chromosome 3 syndrome (disorder)", "Ring chromosome 3 syndrome (diagnosis)", "anomaly of chromosome pair ring chromosome 3 syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ring chromosome 3", "shortest_name_length": 2}
{"curie": "UMLS:C4331319", "names": ["Stage IA Mycosis Fungoides", "Stage IA Mycosis Fungoides AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Mycosis Fungoides AJCC v7", "shortest_name_length": 26}
{"curie": "UMLS:C0236127", "names": ["Bleeding esophageal ulcer", "Bleeding oesophageal ulcer", "Bleeding ulcer of esophagus", "Esophageal ulcer hemorrhage", "Bleeding ulcer of oesophagus", "Oesophageal ulcer haemorrhage", "Hemorrhagic ulcer of esophagus", "ESOPHAGUS ULCERATION HEMORRHAGE", "Esophagus ulceration hemorrhage", "Haemorrhagic ulcer of oesophagus", "ESOPHAGEAL ULCERATION HAEMORRHAG", "esophageal ulcer with hemorrhage", "Ulcer of esophagus with bleeding", "Esophageal ulceration hemorrhage", "OESOPHAGEAL ULCERATION HAEMORRHAG", "Oesophagus ulceration haemorrhage", "Oesophageal ulceration haemorrhage", "Bleeding ulcer of esophagus (disorder)", "esophageal ulcer with hemorrhage (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bleeding ulcer of esophagus", "shortest_name_length": 25}
{"curie": "MONDO:0020019", "names": ["digestive tract malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "digestive tract malformation", "shortest_name_length": 28}
{"curie": "MONDO:0003886", "names": ["Mucinous cystadenofibroma", "Mucinous Cystadenofibroma", "mucinous cystadenofibroma", "mucinous; cystadenofibroma, unspecified site", "cystadenofibroma; mucinous, unspecified site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucinous cystadenofibroma", "shortest_name_length": 25}
{"curie": "UMLS:C4285880", "names": ["Gastric bacterial overgrowth", "Gastrointestinal bacterial overgrowth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal bacterial overgrowth", "shortest_name_length": 28}
{"curie": "MONDO:0044884", "names": ["tonsil lymphoma", "Tonsil Lymphoma", "tonsillar lymphoma", "lymphoma of tonsil", "Lymphoma of Tonsil", "Tonsillar Lymphoma", "lymphoma of the tonsil", "Lymphoma of the Tonsil", "Primary tonsillar lymphoma", "Primary Tonsillar Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tonsillar lymphoma", "shortest_name_length": 15}
{"curie": "UMLS:C0221155", "names": ["sys htn", "systolic htn", "sys hypertension", "Systolic hypertension", "Systolic Hypertension", "systolic hypertension", "HYPERTENSION SYSTOLIC", "hypertension systolic", "SYSTOLIC HYPERTENSION", "Hypertension, Systolic", "Systolic Hypertensions", "Hypertension, systolic", "Systolic hypertension (disorder)", "systolic hypertension (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Systolic Hypertension", "shortest_name_length": 7}
{"curie": "MONDO:0000650", "names": ["Benign Peritoneal Neoplasm", "benign tumor of peritoneum", "benign peritoneal neoplasm", "peritoneum benign neoplasm", "Benign tumor of peritoneum", "Benign peritoneal neoplasm", "peritoneal benign neoplasm", "Benign tumour of peritoneum", "Benign neoplasm of peritoneum", "benign neoplasm of peritoneum", "Benign neoplasm of the peritoneum", "Benign neoplasm of the peritoneum, NOS", "benign neoplasm of peritoneum (diagnosis)", "Benign neoplasm of the peritoneum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peritoneal benign neoplasm", "shortest_name_length": 26}
{"curie": "MONDO:0005905", "names": ["nocturnal myoclonus", "Sleep Myoclonus Syndrome", "Myoclonus Syndrome, Sleep", "Sleep Myoclonus Syndromes", "Syndrome, Sleep Myoclonus", "Myoclonus Syndromes, Sleep", "Syndromes, Sleep Myoclonus", "nocturnal myoclonus syndrome", "Nocturnal Myoclonus Syndrome", "Nocturnal Myoclonus Syndromes", "Myoclonus Syndrome, Nocturnal", "Syndrome, Nocturnal Myoclonus", "disorder limb movement periodic", "Periodic Limb Movement Disorder", "periodic limb movement disorder", "Periodic limb movement disorder", "Periodic Movement Disorder, Sleep", "Sleep Disorder, Periodic Movements", "Periodic limb movement disorder (PLMD)", "Periodic limb movement disorder (disorder)", "Excessive Periodic Sleep Related Leg Movements", "Excessive Periodic Sleep-Related Leg Movements", "Sleep-Related Periodic Leg Movements, Excessive", "Sleep Related Periodic Leg Movements, Excessive", "Periodic Leg Movements, Excessive, Sleep-Related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "periodic limb movement disorder", "shortest_name_length": 19}
{"curie": "MONDO:0043087", "names": ["Schweitzer Kemink Graham syndrome", "thickened earlobes with conductive deafness from incus-stapes abnormalities", "Thickened earlobes with conductive deafness from incus-stapes abnormalities", "conductive hearing loss, middle ear ossicular anomalies, malformed thickened lop auricles, and micrognathia", "Conductive hearing loss, middle ear ossicular anomalies, malformed thickened lop auricles, and micrognathia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thickened earlobes with conductive deafness from incus-stapes abnormalities", "shortest_name_length": 33}
{"curie": "MONDO:0011806", "names": ["OFD", "OSFD", "Osteofibrous Dysplasia", "osteofibrous dysplasia", "Osteofibrous dysplasia", "Kempson-Campanacci lesion", "Kempson-Campanacci Lesion", "cortical fibrous dysplasia", "Osteofibrous Dysplasia of Bone", "osteofibrous dysplasia of bone", "ossifying fibroma of long bones", "Ossifying Fibroma of Long Bones", "Osteofibrous dysplasia (disorder)", "OSTEOFIBROUS DYSPLASIA, SUSCEPTIBILITY TO", "osteofibrous dysplasia, susceptibility to", "TIBIA, BOWING OF, WITH PSEUDARTHROSIS AND PECTUS EXCAVATUM", "tibia, bowing of, with pseudarthrosis and pectus excavatum", "Tibia, Bowing of, with Pseudarthrosis and Pectus Excavatum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteofibrous dysplasia", "shortest_name_length": 3}
{"curie": "UMLS:C2983696", "names": ["Uterine Corpus Cancer by AJCC v6 Stage", "Uterine Corpus Carcinoma or Carcinosarcoma by AJCC v6 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Corpus Cancer by AJCC v6 Stage", "shortest_name_length": 38}
{"curie": "UMLS:C2938875", "names": ["Upper-airway cough syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Upper-airway cough syndrome", "shortest_name_length": 27}
{"curie": "MONDO:0016423", "names": ["APS4", "APS type 4", "autoimmune polyendocrinopathy type 4", "Autoimmune polyendocrinopathy type 4", "autoimmune polyglandular syndrome type 4", "Autoimmune polyendocrine syndrome type 4", "Autoimmune polyglandular syndrome type 4", "autoimmune polyendocrine syndrome type 4", "Autoimmune polyendocrine syndrome type 4 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune polyendocrinopathy type 4", "shortest_name_length": 4}
{"curie": "MONDO:0017902", "names": ["autosomal recessive MSMD due to partial IFNgammaR2 deficiency", "autosomal recessive MSMD due to partial interferon gamma receptor 2 deficiency", "IFNGR2 autosomal recessive mendelian susceptibility to mycobacterial diseases due to a partial deficiency", "autosomal recessive Mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency", "autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 2 deficiency", "autosomal recessive mendelian susceptibility to mycobacterial diseases due to a partial deficiency caused by mutation in IFNGR2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive Mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency", "shortest_name_length": 61}
{"curie": "MONDO:0019674", "names": ["PAPB", "postaxial polydactyly type B", "Postaxial polydactyly type B", "POSTAXIAL POLYDACTYLY, TYPE B", "Postaxial polydactyly, type B", "Postaxial Polydactyly, Type B", "Postaxial polydactyly type B (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postaxial polydactyly type B", "shortest_name_length": 4}
{"curie": "UMLS:C5666803", "names": ["pHGG MYCN", "Diffuse Pediatric-Type High Grade Glioma MYCN", "Diffuse Pediatric-Type High-Grade Glioma MYCN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse Pediatric-Type High Grade Glioma MYCN", "shortest_name_length": 9}
{"curie": "UMLS:C3274789", "names": ["Structural Heart Abnormality"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Structural Heart Abnormality", "shortest_name_length": 28}
{"curie": "UMLS:C0236053", "names": ["Mucosal sores", "Mucosal ulcer", "Mucosal Ulcer", "mucosal ulcer", "mucosal sores", "MUCOSAL SORES", "Mucosal ulcers", "mucosal ulcers", "Mucosal ulceration", "mucosal ulceration", "MUCOSAL ULCERATION", "Mucosal ulcerations", "Mucous membrane ulcer", "Mucosal ulceration NOS", "membrane mucous ulcers", "Mucosal ulcer (disorder)", "MUCOUS MEMBRANE ULCERATION", "Mucous membrane ulceration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mucosal ulcer", "shortest_name_length": 13}
{"curie": "UMLS:C2111706", "names": ["Anal Large Cell NEC", "Anal Canal Large Cell NEC", "Anal Large Cell Neuroendocrine Carcinoma", "Anal Canal Large Cell Neuroendocrine Carcinoma", "large cell neuroendocrine carcinoma of anal canal", "large cell neuroendocrine carcinoma of anal canal (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "large cell neuroendocrine carcinoma of anal canal", "shortest_name_length": 19}
{"curie": "MONDO:0008136", "names": ["ONH", "hypoplasia optic nerve", "Optic Nerve Hypoplasia", "Optic nerve hypoplasia", "optic nerve hypoplasia", "Hypoplasia, Optic Nerve", "Hypoplastic optic nerves", "Hypoplasia of optic nerve", "Underdeveloped optic nerves", "ONH - Optic nerve hypoplasia", "Hypoplasia of the Optic Nerve", "Hypoplasia of the optic nerve", "Optic Nerve Aplasia, Bilateral", "optic nerve aplasia, bilateral", "OPTIC NERVE APLASIA, BILATERAL", "isolated optic nerve hypoplasia", "Isolated optic nerve hypoplasia", "bilateral optic nerve hypoplasia", "Bilateral Optic Nerve Hypoplasia", "Optic Nerve Hypoplasia, Bilateral", "Optic nerve hypoplasia, bilateral", "optic nerve hypoplasia, bilateral", "OPTIC NERVE HYPOPLASIA, BILATERAL", "optic nerve hypoplasia (diagnosis)", "isolated optic nerve hypoplasia/aplasia", "Optic nerve hypoplasia, unspecified eye", "Bilateral Hypoplasia of the Optic Nerve", "Hypoplasia of the Optic Nerve, Bilateral", "Hypoplasia of the optic nerve (disorder)", "familial bilateral optic nerve hypoplasia", "optic nerve hypoplasia, familial bilateral", "Isolated optic nerve hypoplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated optic nerve hypoplasia", "shortest_name_length": 3}
{"curie": "UMLS:C0520777", "names": ["PELVIC INFLAMMATORY DISEASE CHLAMYDIA", "Pelvic inflammatory disease chlamydial", "Chlamydial pelvic inflammatory disease", "Chlamydial pelvic inflammatory disease (disorder)", "pelvic inflammatory disease due to Chlamydia trachomatis", "pelvic inflammatory disease due to Chlamydia trachomatis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chlamydial pelvic inflammatory disease", "shortest_name_length": 37}
{"curie": "UMLS:C1335731", "names": ["Refractory T-Lymphoblastic Lymphoma", "Refractory T Lymphoblastic Lymphoma", "Refractory Precursor T-Lymphoblastic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory T Lymphoblastic Lymphoma", "shortest_name_length": 35}
{"curie": "UMLS:C1167675", "names": ["Application site folliculitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Application site folliculitis", "shortest_name_length": 29}
{"curie": "MONDO:0020666", "names": ["Löfgren syndrome", "Löfgrens syndrome", "Lofgrens syndrome", "Loefgren syndrome", "Loefgrens syndrome", "Lofgren's syndrome", "Lofgrens syndrome (disorder)", "Bilateral hilar adenopathy syndrome", "Bilateral hilar adenopathy syndrome (disorder)", "Bilateral hilar lymph node sarcoidosis with erythema nodosum", "Erythema nodosum with bilateral hilar lymph node sarcoidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Löfgren syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0004976", "names": ["ALS", "Gehrig Disease", "Charcot Disease", "Gehrigs Disease", "palsy; creeping", "Charcot disease", "creeping; palsy", "Gehrig's Disease", "LOU GEHRIG DISEASE", "Lou Gehrig disease", "Lou Gehrig Disease", "lou gehrig disease", "lou gehrigs disease", "Lou-Gehrigs Disease", "Lou Gehrig's Disease", "lou gehrig's disease", "Lou Gehrig's disease", "Disease, Lou-Gehrigs", "Lou Gehrig's disease (ALS)", "Bulbar motor neuron disease", "Motor neuron disease, bulbar", "motor neuron disease, bulbar", "Amytrophic lateral sclerosis", "lateral sclerosis; amyotrophy", "Amyotrophic Lateral Sclerosis", "Amyotrophic lateral sclerosis", "AMYOTROPHIC LATERAL SCLEROSIS", "amyotrophy; lateral sclerosis", "amyotrophic lateral sclerosis", "amyotrophic laterals sclerosis", "Sclerosis, Amyotrophic Lateral", "ALS Amyotrophic Lateral Sclerosis", "ALS - Amyotrophic Lateral Sclerosis", "ALS (amyotrophic lateral sclerosis)", "ALS - Amyotrophic lateral sclerosis", "obsolete_amyotrophic lateral sclerosis", "spinal; sclerosis, lateral (amyotrophic)", "sclerosis; spinal, lateral (amyotrophic)", "Amyotrophic lateral sclerosis (disorder)", "amyotrophic lateral sclerosis (diagnosis)", "Motor Neuron Disease, Amyotrophic Lateral Sclerosis", "Amyotrophic Lateral Sclerosis/Progressive Muscular Atrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyotrophic lateral sclerosis", "shortest_name_length": 3}
{"curie": "UMLS:C5419764", "names": ["Unresectable Salivary Gland Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Salivary Gland Squamous Cell Carcinoma", "shortest_name_length": 51}
{"curie": "UMLS:C1334728", "names": ["Metastatic Tumor to the Iris", "Metastatic Neoplasm to the Iris", "Metastatic Malignant Neoplasm to the Iris", "Metastatic Malignant Neoplasm in the Iris"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Malignant Neoplasm in the Iris", "shortest_name_length": 28}
{"curie": "UMLS:C0241426", "names": ["Glossopyroses", "glossopyrosis", "Glossopyrosis", "Burn of tongue", "tongue burning", "Burning tongue", "burning tongue", "burning; tongue", "tongue; burning", "Glossopyrosis (disorder)", "TONGUE BURNING SENSATION", "burning sensation tongue"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Burning tongue", "shortest_name_length": 13}
{"curie": "UMLS:C1512253", "names": ["FIGO Grade 2 Endometrial Mucinous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Grade 2 Endometrial Mucinous Adenocarcinoma", "shortest_name_length": 48}
{"curie": "MONDO:0019979", "names": ["renal hypoplasia, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal hypoplasia, unilateral", "shortest_name_length": 28}
{"curie": "MONDO:0013015", "names": ["BRGDA5", "Brugada syndrome 5", "BRUGADA SYNDROME 5", "Brugada Syndrome 5", "SCN1B Brugada syndrome", "Brugada syndrome type 5", "Brugada syndrome 5 (diagnosis)", "Cardiac conduction defect, nonspecific", "CARDIAC CONDUCTION DEFECT, NONSPECIFIC", "Cardiac Conduction Defect, Nonspecific", "Brugada syndrome caused by mutation in SCN1B", "CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brugada syndrome 5", "shortest_name_length": 6}
{"curie": "UMLS:C5446580", "names": ["Resectable Leiomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Leiomyosarcoma", "shortest_name_length": 25}
{"curie": "MONDO:0018771", "names": ["congenital ventricular septal anomaly", "congenital anomaly of ventricular septum", "rare congenital anomaly of ventricular septum", "congenital anomaly of interventricular communication", "interventricular septum congenital heart malformation", "congenital heart malformation of interventricular septum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital anomaly of ventricular septum", "shortest_name_length": 37}
{"curie": "MONDO:0019583", "names": ["localized lichen myxedematosus with mixed features of different subtypes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "localized lichen myxedematosus with mixed features of different subtypes", "shortest_name_length": 72}
{"curie": "UMLS:C0862967", "names": ["Cholangiocarcinoma recurrent", "Recurrent Cholangiocarcinoma", "Recurrent Cholangiocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cholangiocarcinoma recurrent", "shortest_name_length": 28}
{"curie": "UMLS:C0751118", "names": ["Familial Tonic Clonic Epilepsy", "Familial Tonic-Clonic Epilepsy", "Tonic-Clonic Epilepsy, Familial", "Epilepsy, Familial Tonic-Clonic", "Familial Tonic-Clonic Epilepsies", "Epilepsy, Tonic-Clonic, Familial", "Epilepsies, Familial Tonic-Clonic", "Tonic-Clonic Epilepsies, Familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epilepsy, Tonic-Clonic, Familial", "shortest_name_length": 30}
{"curie": "UMLS:C2875024", "names": ["Cerebral Ventriculitis", "Ventriculitis, Cerebral", "Cerebral Ventriculitides", "Ventriculitides, Cerebral", "Ventriculitis (cerebral) NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebral Ventriculitis", "shortest_name_length": 22}
{"curie": "MONDO:0001643", "names": ["Ballet's disease", "exophthalmic ophthalmoplegia", "Exophthalmic ophthalmoplegia", "Exophthalmic ophthalmoplegia (disorder)", "exophthalmic ophthalmoplegia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exophthalmic ophthalmoplegia", "shortest_name_length": 16}
{"curie": "UMLS:C0948920", "names": ["Tuberculoma of central nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tuberculoma of central nervous system", "shortest_name_length": 37}
{"curie": "MONDO:0010488", "names": ["MRX100", "XLID100", "X-linked mental retardation 100", "mental retardation, X-linked 100", "MENTAL RETARDATION, X-LINKED 100", "mental retardation, X-linked type 100", "intellectual disability, X-linked 100", "intellectual disability, X-linked type 100", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 100", "non-syndromic X-linked intellectual disability 100", "KIF4A non-syndromic X-linked intellectual disability", "intellectual developmental disorder, X-linked 100, X-linked recessive", "non-syndromic X-linked intellectual disability caused by mutation in KIF4A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 100", "shortest_name_length": 6}
{"curie": "UMLS:C4329966", "names": ["Factor IX Inactivation", "Factor IX Inhibitor Present"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Factor IX Inactivation", "shortest_name_length": 22}
{"curie": "MONDO:0008071", "names": ["AORF", "RFH1", "Familial nephropathy", "nephropathy, familial", "NEPHROPATHY, FAMILIAL", "Nephropathy, Familial", "nephropathy-hypertension", "Renal Failure, Adult-Onset", "RENAL FAILURE, ADULT-ONSET", "renal failure, adult-onset", "Renal Failure, Progressive, with Hypertension", "renal failure, progressive, with hypertension", "RENAL FAILURE, PROGRESSIVE, WITH HYPERTENSION", "Nephritis, Familial, without Deafness or Ocular Defect", "NEPHRITIS, FAMILIAL, WITHOUT DEAFNESS OR OCULAR DEFECT", "nephritis, familial, without deafness or ocular defect", "Progressive hereditary glomerulonephritis without deafness", "progressive hereditary glomerulonephritis without deafness", "Autosomal dominant progressive nephropathy with hypertension", "autosomal dominant progressive nephropathy with hypertension", "Progressive hereditary glomerulonephritis without deafness (disorder)", "progressive hereditary glomerulonephritis without deafness (diagnosis)", "Autosomal dominant progressive nephropathy with hypertension (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant progressive nephropathy with hypertension", "shortest_name_length": 4}
{"curie": "MONDO:0013275", "names": ["glucosephosphate isomerase deficiency", "hemolytic anemia due to glucophosphate isomerase deficiency", "HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY", "hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemolytic anemia due to glucophosphate isomerase deficiency", "shortest_name_length": 37}
{"curie": "MONDO:0100002", "names": ["FPIPC", "allergic proctocolitis", "milk protein proctocololitis", "food protein-induced allergic proctocolitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "food protein-induced allergic proctocolitis", "shortest_name_length": 5}
{"curie": "UMLS:C5230922", "names": ["Acral nevus", "Acral Nevus", "Acral naevus", "Acral Skin Nevus", "Nevus of Acral Skin", "Acral nevus (disorder)", "Acral nevus (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acral nevus", "shortest_name_length": 11}
{"curie": "MONDO:0026722", "names": ["MKMS", "NEDXCF", "Mullegama-Klein-Martinez syndrome", "MULLEGAMA-KLEIN-MARTINEZ SYNDROME", "X-linked neurodevelopmental disorder with craniofacial abnormalities", "Neurodevelopmental Disorder, X-Linked, With Craniofacial Abnormalities", "NEURODEVELOPMENTAL DISORDER, X-LINKED, WITH CRANIOFACIAL ABNORMALITIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mullegama-Klein-Martinez syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0700066", "names": ["FKRP myopathy", "FKRP-related myopathy", "myopathy caused by mutation in FKRP", "myopathy caused by variation in FKRP"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy caused by variation in FKRP", "shortest_name_length": 13}
{"curie": "UMLS:C4321446", "names": ["PNDM", "K ATP Permanent Neonatal Diabetes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "K ATP Permanent Neonatal Diabetes", "shortest_name_length": 4}
{"curie": "MONDO:0019345", "names": ["Flexner", "shigella", "Shigella", "shigellas", "SHIGELLOSES", "shigellosis", "SHIGELLOSIS", "Shigellosis", "Hiss-Russell", "Shigella boydii", "dysentery; Boyd", "Boyd; dysentery", "Shigellosis, NOS", "Shigella flexneri", "Bacillus; Flexner", "shigella dysentery", "Shigella Infection", "shigella infection", "dysentery; Flexner", "Japanese dysentery", "japanese dysentery", "Flexner; dysentery", "Shigella infection", "Shigella Dysentery", "Shigella dysentery", "dysentery; Shigella", "SHIGA-KRUSE DISEASE", "Shigella Infections", "Shigella; infection", "BACILLARY DYSENTERY", "Bacillary dysentery", "Infection, Shigella", "Shigella; dysentery", "bacillary dysentery", "dysentery bacillary", "infection; Shigella", "Dysentery, Shigella", "Shigella infections", "Dysentery;bacillary", "Bacillary Dysentery", "flexner's dysentery", "Flexner's dysentery", "bacillary; dysentery", "dysentery; bacillary", "Shigella dysenteriae", "Dysentery, Bacillary", "Shigella Dysenteries", "Infections, Shigella", "Infection by Shigella", "Dysenteries, Shigella", "Shigellosis (disorder)", "shigellosis (diagnosis)", "Hiss-Russell; dysentery", "Bacillary dysentery NOS", "dysentery; Hiss-Russell", "Shigellosis, unspecified", "GASTROENTERITIS SHIGELLA", "Shigella gastroenteritis", "Gastroenteritis shigella", "dysentery; bacillary, Boyd", "bacillary; dysentery, Boyd", "Shigella group A enteritis", "Shigella boydii shigellosis", "infection; Bacillus Flexner", "infection; Shigella, boydii", "Shigella; infection, boydii", "infection; Shigella, shigae", "Shigella; infection, shigae", "Infection caused by Shigella", "infection; Shigella, group, A", "Infection by group B Shigella", "infection; Shigella, group, C", "Shigella flexneri shigellosis", "bacillary; dysentery, Flexner", "Shigella; infection, group, A", "dysentery; bacillary, Flexner", "Infection by group C Shigella", "Shigella; infection, flexneri", "infection; Shigella, group, B", "Shigella; infection, group, C", "infection; Shigella, flexneri", "Infection by group A Shigella", "Shigella; infection, group, B", "bacillary; dysentery, Shigella", "dysentery; bacillary, Shigella", "Bacillary dysentery (disorder)", "bacillary dysentery (diagnosis)", "infection; Shigella, dysenteriae", "Shigella dysenteriae shigellosis", "Shigella; infection, dysenteriae", "Infection due to Group C Shigella", "Infection due to Group A Shigella", "Infection due to Group B Shigella", "shigellosis due to Shigella boydii", "Shigella boydii infectious disease", "Shigellosis due to Shigella boydii", "Shigella sonnei infectious disease", "Shigella flexneri infectious disease", "Infection caused by Group C Shigella", "Infection caused by Group B Shigella", "Infection caused by Group A Shigella", "shigellosis due to Shigella flexneri", "Shigellosis due to Shigella flexneri", "Shigellosis caused by Shigella boydii", "Disease caused by Shigella dysenteriae", "dysentery; bacillary, Shigella, boydii", "bacillary; dysentery, Shigella, boydii", "dysentery; bacillary, Shigella, group B", "Shigellosis caused by Shigella flexneri", "Infection caused by Shigella (disorder)", "dysentery; bacillary, Shigella, group C", "dysentery; bacillary, Shigella, group A", "bacillary; dysentery, Shigella, group A", "Shigellosis due to Shigella dysenteriae", "bacillary; dysentery, Shigella, group B", "shigellosis due to Shigella dysenteriae", "bacillary; dysentery, Shigella, group C", "bacillary; dysentery, Shigella, flexneri", "dysentery; bacillary, Shigella, flexneri", "Shigellosis caused by Shigella dysenteriae", "bacillary; dysentery, Shigella, dysenteriae", "dysentery; bacillary, Shigella, dysenteriae", "Infection due to Group A Shigella (diagnosis)", "shigellosis due to Shigella boydii (diagnosis)", "Infection caused by Group A Shigella (disorder)", "Infection caused by Group C Shigella (disorder)", "Infection caused by Group B Shigella (disorder)", "shigellosis due to Shigella flexneri (diagnosis)", "shigellosis due to Shigella dysenteriae (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "shigellosis", "shortest_name_length": 7}
{"curie": "MONDO:0007853", "names": ["Keratoderma palmoplantar spastic paralysis", "Axonal neuropathy with palmoplantar keratoderma", "AXONAL NEUROPATHY WITH PALMOPLANTAR KERATODERMA", "axonal neuropathy with palmoplantar keratoderma", "Palmoplantar keratoderma-Charcot-Marie-Tooth syndrome", "Palmoplantar keratoderma, Charcot-Marie-Tooth syndrome", "Palmoplantar keratoderma-hereditary motor and sensory neuropathy syndrome", "palmoplantar keratoderma-hereditary motor and sensory neuropathy syndrome", "Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome", "CHARCOT-MARIE-TOOTH DISEASE WITH PALMOPLANTAR KERATODERMA AND NAIL DYSTROPHY", "Charcot-Marie-Tooth disease with palmoplantar keratoderma and nail dystrophy", "Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome (disorder)", "keratoderma, palmoplantar, with nail dystrophy and hereditary motor-sensory neuropathy", "KERATODERMA, PALMOPLANTAR, WITH NAIL DYSTROPHY AND HEREDITARY MOTOR-SENSORY NEUROPATHY", "Keratoderma, palmoplantar, with nail dystrophy and hereditary motor-sensory neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "palmoplantar keratoderma-hereditary motor and sensory neuropathy syndrome", "shortest_name_length": 42}
{"curie": "MONDO:0018424", "names": ["lipoate biosynthesis defect", "lipoic acid biosynthesis defect", "lipoic acid biosynthesis defects", "inherited lipoic acid biosynthesis defect", "inborn lipoate biosynthetic process disorder", "inborn error of lipoate biosynthetic process", "rare inborn error of lipoate biosynthetic process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited lipoic acid biosynthesis defect", "shortest_name_length": 27}
{"curie": "UMLS:C4725913", "names": ["Lymphoproliferative Disease Associated with PID", "Lymphoproliferative Disease Associated with Primary Immune Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoproliferative Disease Associated with Primary Immune Disorder", "shortest_name_length": 47}
{"curie": "UMLS:C0456877", "names": ["High Grade T-Cell Lymphoma", "High grade T-cell lymphoma", "High grade T-cell lymphoma (disorder)", "High grade T-cell lymphoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High grade T-cell lymphoma", "shortest_name_length": 26}
{"curie": "MONDO:0019401", "names": ["sporadic idiopathic nephrosis", "Sporadic idiopathic nephrosis", "sporadic idiopathic steroid-resistant nephrotic syndrome", "Sporadic idiopathic steroid-resistant nephrotic syndrome", "Sporadic idiopathic steroid-resistant nephrotic syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sporadic idiopathic steroid-resistant nephrotic syndrome", "shortest_name_length": 29}
{"curie": "MONDO:0032869", "names": ["MC5DN6", "mitochondrial complex V (ATP synthase) deficiency nuclear type 6", "MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 6", "mitochondrial complex 5 (ATP synthase) deficiency, nuclear type 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 5 (ATP synthase) deficiency, nuclear type 6", "shortest_name_length": 6}
{"curie": "MONDO:0011211", "names": ["SMDAX", "SmD axial", "AXIAL SMD", "Axial SMD", "SMD axial", "axial SmD", "SMD, AXIAL", "SMD, Axial", "SmD, axial", "axial spondylometaphyseal dysplasia", "Axial spondylometaphyseal dysplasia", "spondylometaphyseal dysplasia, axial", "SPONDYLOMETAPHYSEAL DYSPLASIA, AXIAL", "Spondylometaphyseal dysplasia, axial", "spondylometaphyseal dysplasia axial type", "Axial spondylometaphyseal dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "axial spondylometaphyseal dysplasia", "shortest_name_length": 5}
{"curie": "MONDO:0005074", "names": ["Papillocystic adenocarcinoma", "papillary cystadenocarcinoma", "Papillary Cystadenocarcinoma", "Papillary cystadenocarcinoma", "Papillary Cystadenocarcinomas", "Cystadenocarcinoma, Papillary", "Cystadenocarcinomas, Papillary", "Papillary cystadenocarcinoma NOS", "Papillary cystadenocarcinoma, NOS", "cystadenocarcinoma, papillary, malignant", "CYSTADENOCARCINOMA, PAPILLARY, MALIGNANT", "cystadenocarcinoma; papillary, unspecified site", "papillary; cystadenocarcinoma, unspecified site", "Papillary cystadenocarcinoma (morphologic abnormality)", "papillary cystadenocarcinoma (morphologic abnormality)", "papillary cystadenocarcinoma, NOS (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papillary cystadenocarcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0012029", "names": ["MCPH6", "primary autosomal recessive microcephaly 6", "Microcephaly, Primary Autosomal Recessive, 6", "microcephaly 6, primary, autosomal recessive", "MICROCEPHALY 6, PRIMARY, AUTOSOMAL RECESSIVE", "CENPJ autosomal recessive primary microcephaly", "autosomal recessive primary microcephaly caused by mutation in CENPJ"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly 6, primary, autosomal recessive", "shortest_name_length": 5}
{"curie": "MONDO:0024459", "names": ["Aeromonas hydrophila intestinal disease", "intestinal infection due to Aeromonas hydrophila", "Intestinal infection due to Aeromonas hydrophila", "intestinal infection due to Aeromonas hydrophilia", "intestinal infection caused by Aeromonas hydrophila", "Intestinal infection caused by Aeromonas hydrophila", "intestinal infections bacterial aeromonas hydrophilia", "intestinal infection due to Aeromonas hydrophilia (diagnosis)", "Intestinal infection caused by Aeromonas hydrophila (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aeromonas hydrophila intestinal disease", "shortest_name_length": 39}
{"curie": "MONDO:0013225", "names": ["CGL4", "GCL4", "BSCL4", "congenital generalized lipodystrophy type 4", "Generalised congenital lipodystrophy type 4", "generalised congenital lipodystrophy type 4", "generalized congenital lipodystrophy type 4", "Generalized congenital lipodystrophy type 4", "congenital generalised lipodystrophy type 4", "LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4", "lipodystrophy, congenital generalized, type 4", "Lipodystrophy, Congenital Generalized, Type 4", "generalised congenital lipodystrophy with myopathy", "Generalized congenital lipodystrophy with myopathy", "generalized congenital lipodystrophy with myopathy", "Generalised congenital lipodystrophy with myopathy", "CAVIN1 congenital generalized lipodystrophy (disease)", "Generalized congenital lipodystrophy with myopathy (disorder)", "Berardinelli-Seip congenital lipodystrophy type 4 with muscular dystrophy", "congenital generalized lipodystrophy (disease) caused by mutation in CAVIN1", "Berardinelli-Seip congenital lipodystrophy, type 4, with muscular dystrophy", "BERARDINELLI-SEIP CONGENITAL LIPODYSTROPHY, TYPE 4, WITH MUSCULAR DYSTROPHY", "Berardinelli-Seip Congenital Lipodystrophy, Type 4, With Muscular Dystrophy", "LIPODYSTROPHY, BERARDINELLI-SEIP CONGENITAL, TYPE 4, WITH MUSCULAR DYSTROPHY", "Lipodystrophy, Berardinelli-Seip Congenital, Type 4, With Muscular Dystrophy", "lipodystrophy, Berardinelli-Seip congenital, type 4, with muscular dystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital generalized lipodystrophy type 4", "shortest_name_length": 4}
{"curie": "MONDO:0014505", "names": ["DEE27", "EIEE27", "early infantile epileptic encephalopathy 27", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 27", "developmental and epileptic encephalopathy 27", "epileptic encephalopathy, early infantile, 27", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 27", "developmental and epileptic encephalopathy, 27", "GRIN2B early infantile epileptic encephalopathy", "epileptic encephalopathy, early infantile, type 27", "early infantile epileptic encephalopathy caused by mutation in GRIN2B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 27", "shortest_name_length": 5}
{"curie": "UMLS:C1611171", "names": ["Thalamic infarction", "cerebral infarction thalamic", "Thalamic infarction (disorder)", "Thalamic infarction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thalamic infarction", "shortest_name_length": 19}
{"curie": "UMLS:C1708557", "names": ["Intrapulmonary Thymoma", "Intrapulmonary thymoma", "Intrapulmonary thymoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intrapulmonary thymoma", "shortest_name_length": 22}
{"curie": "UMLS:C1883282", "names": ["Testicular Typical Seminoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular Typical Seminoma", "shortest_name_length": 27}
{"curie": "MONDO:0010407", "names": ["JMS", "MRXST", "MRXSBWB", "MRXS-Turner", "Brooks syndrome", "JUBERG-MARSIDI SYNDROME", "Juberg-Marsidi Syndrome", "Juberg-Marsidi syndrome", "Juberg Marsidi syndrome", "Juberg-Marsidi syndrome (JMS)", "Brooks-Wisniewski-Brown Syndrome", "Brooks Wisniewski Brown syndrome", "BROOKS-WISNIEWSKI-BROWN SYNDROME", "Brooks-Wisniewski-Brown syndrome", "Juberg Marsidi syndrome (disorder)", "Juberg Marsidi syndrome (diagnosis)", "X-linked mental retardation Brooks type", "Juberg-Marsidi Mental Retardation Syndrome", "[OBSOLETE] Brooks-Wisniewski-Brown Syndrome", "mental retardation and macrocephaly syndrome", "X-linked intellectual disability Brooks type", "MENTAL RETARDATION AND MACROCEPHALY SYNDROME", "Mental Retardation and Macrocephaly Syndrome", "X-linked intellectual disability, Turner type", "X-linked intellectual disability, Brooks type", "mental retardation, X-linked syndromic, Turner type", "Mental Retardation, X-Linked, Syndromic, Turner Type", "MENTAL RETARDATION, X-LINKED, SYNDROMIC, TURNER TYPE", "mental retardation, X-linked, syndromic, Turner type", "syndromic X-linked intellectual disability Turner type", "X-linked intellectual disability Brooks type (disorder)", "intellectual disability, X-linked syndromic, Turner type", "X-linked intellectual disability, Brooks type (diagnosis)", "MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, TURNER TYPE", "mental retardation, X-linked, syndromic, Brooks-Wisniewski-Brown type", "mental retardation, X-linked, syndromic, Brooks-Wisniewski-Brown Type", "X-linked mental retardation-growth retardation-deafness-microgenitalism syndrome", "mental retardation, X-Linked, with growth retardation, deafness, and microgenitalism", "MENTAL RETARDATION, X-LINKED, WITH GROWTH RETARDATION, DEAFNESS, AND MICROGENITALISM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked syndromic, Turner type", "shortest_name_length": 3}
{"curie": "MONDO:0007545", "names": ["EOSINOPHILOPENIA", "Eosinophilopenia", "EOSINOPHIL APLASIA", "eosinophil aplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eosinophilopenia", "shortest_name_length": 16}
{"curie": "UMLS:C1963905", "names": ["Infantile free sialic acid storage disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infantile free sialic acid storage disease", "shortest_name_length": 42}
{"curie": "UMLS:C3897615", "names": ["Simple Tic", "Simple tic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Simple tic", "shortest_name_length": 10}
{"curie": "MONDO:0002832", "names": ["Endometrial Transitional Cell Carcinoma", "endometrial transitional cell carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometrial transitional cell carcinoma", "shortest_name_length": 39}
{"curie": "MONDO:0024530", "names": ["BTHLM1", "Bethlem myopathy", "Bethlem myopathy 1", "muscular dystrophy, benign congenital", "myopathy, benign congenital, with contractures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bethlem myopathy 1", "shortest_name_length": 6}
{"curie": "MONDO:0002305", "names": ["Thrombophilia", "thrombophilia", "thrombophilias", "Thrombophilias", "Hypercoagulable", "hypercoagulable", "Hypercoagulation", "HYPERCOAGULATION", "hypercoagulation", "Thrombophilia NOS", "hypercoagulability", "Hypercoagulability", "Blood hyperviscosity", "Hypercoagulabilities", "HYPERCOAGULABLE STATE", "hypercoagulable state", "Hypercoagulable state", "hypercoagulable states", "Hypercoagulability State", "Hypercoagulability state", "Thrombophilia (disorder)", "hypercoagulability state", "excessive blood clotting", "Excessive Blood Clotting", "hypercoagulability states", "Hypercoagulable state NOS", "thrombophilia (diagnosis)", "Hypercoagulability state, NOS", "Hypercoagulability state (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombophilia", "shortest_name_length": 13}
{"curie": "MONDO:0001791", "names": ["Urinary tract infection neonatal", "URINARY TRACT INFECTION NEONATAL", "Neonatal urinary tract infection", "newborn; infection urinary tract", "urinary tract; infection, newborn", "infection; urinary tract, newborn", "urinary tract infection of newborn", "Urinary tract infection of newborn", "Urinary tract infection NOS neonatal", "neonatal urinary tract infectious disease", "Neonatal urinary tract infection (disorder)", "urinary tract infection of newborn (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal urinary tract infectious disease", "shortest_name_length": 32}
{"curie": "MONDO:0008836", "names": ["ATAXIA WITH MYOCLONIC EPILEPSY AND PRESENILE DEMENTIA", "Ataxia with Myoclonic Epilepsy and Presenile Dementia", "ataxia with myoclonic epilepsy and presenile dementia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ataxia with myoclonic epilepsy and presenile dementia", "shortest_name_length": 53}
{"curie": "MONDO:0016016", "names": ["Toluene embryopathy", "toluene embryopathy", "Fetal toluene syndrome", "Foetal toluene syndrome", "Hersh Podruch Weisskopk syndrome", "Fetal toluene syndrome (disorder)", "microcephaly, central nervous system dysfunction, minor craniofacial and limb anomalies, and variable growth deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "toluene embryopathy", "shortest_name_length": 19}
{"curie": "UMLS:C4048610", "names": ["Cardiac procedure complication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiac procedure complication", "shortest_name_length": 30}
{"curie": "MONDO:0018163", "names": ["ARCL2A", "cutis laxa, debre type", "cutis laxa with bone dystrophy", "autosomal recessive cutis laxa type 2A", "cutis laxa, autosomal recessive type 2A", "autosomal recessive cutis laxa type IIA", "cutis laxa, autosomal recessive, type 2A", "cutis laxa, autosomal recessive, type IIA", "cutis laxa with growth and developmental delay", "cutis laxa with congenital disorder of glycosylation", "cutis laxa with Joint laxity and retarded development"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive cutis laxa type 2A", "shortest_name_length": 6}
{"curie": "UMLS:C1696114", "names": ["Stubbornness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stubbornness", "shortest_name_length": 12}
{"curie": "UMLS:C1334229", "names": ["Bowel Dysplasia", "Intestinal Dysplasia", "Intestinal Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal Intraepithelial Neoplasia", "shortest_name_length": 15}
{"curie": "UMLS:C3658290", "names": ["Drug Induced Acute Liver Injury", "Drug-Induced Acute Liver Injury", "Acute Liver Injury, Drug-Induced", "Acute Liver Injury, Drug Induced", "Liver Injury, Drug-Induced, Acute"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drug-Induced Acute Liver Injury", "shortest_name_length": 31}
{"curie": "MONDO:0016025", "names": ["MAE", "mae", "EMAS", "Doose syndrome", "Dooze syndrome", "Doose Syndrome", "Myoclonic atonic seizure", "Myoclonic-astatic seizure", "Myoclonic atonic epilepsy", "Myoclonic-atonic seizures", "myoclonic atonic epilepsy", "Myoclonic atonic seizures", "Myoclonic Astatic Epilepsy", "Myoclonic astatic epilepsy", "myoclonic astatic epilepsy", "Myoclonic-astatic epilepsy", "Myoclonic-astatic seizures", "Epilepsy, Myoclonic Astatic", "Astatic Epilepsy, Myoclonic", "myoclonic-astastic epilepsy", "Myoclonic Astatic Epilepsies", "Astatic Epilepsies, Myoclonic", "Epilepsies, Myoclonic Astatic", "epilepsy; myoclonic-astatic seizures", "Generalised myoclonic-atonic seizure", "Generalized myoclonic-atonic seizure", "myoclonic-astatic seizures; epileptic", "epilepsy with myoclono-astatic crisis", "Myoclonic astatic epilepsy (disorder)", "Myoclonic astatic epilepsy (diagnosis)", "epilepsy with myoclonic-atonic seizures", "Epilepsy with myoclonic-atonic seizures", "epilepsy with myoclonic-astatic seizures", "Epilepsy with myoclonic-astatic seizures", "Epilepsy with myoclonic and astatic seizures", "myoclonic-astatic epilepsy in early childhood", "Myoclonic-astatic epilepsy in early childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myoclonic-astastic epilepsy", "shortest_name_length": 3}
{"curie": "UMLS:C5419747", "names": ["Skin Malignant Peripheral Nerve Sheath Tumor", "Dermal Malignant Peripheral Nerve Sheath Tumor", "Cutaneous Malignant Peripheral Nerve Sheath Tumor", "Malignant Peripheral Nerve Sheath Tumor of the Skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Peripheral Nerve Sheath Tumor of the Skin", "shortest_name_length": 44}
{"curie": "MONDO:0044632", "names": ["Ecca", "ECAA", "extracranial carotid artery aneurysm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "extracranial carotid artery aneurysm", "shortest_name_length": 4}
{"curie": "UMLS:C1333445", "names": ["Esophageal Fibroma", "Fibroma of Esophagus", "Fibroma of the Esophagus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Fibroma", "shortest_name_length": 18}
{"curie": "MONDO:0009256", "names": ["GALACTORRHEA", "Galactorrhea", "galactorrhea", "GALACTORRHOEA", "Galactorrheas", "galactorrhoea", "Galactorrhoea", "Precocious udder", "Nipple Discharge", "Galactorrhea, NOS", "Galactorrhea female", "GALACTORRHEA FEMALE", "Precocious lactation", "Galactorrhoea female", "Galactorrhea syndrome", "galactorrhea syndrome", "LACTATION NONPUERPERAL", "galactorrhea (disease)", "Lactation non-puerperal", "nonpuerperal; lactation", "lactation; nonpuerperal", "Inappropriate lactation", "GALACTORRHEA NONOBSTETRIC", "nonpuerperal galactorrhea", "Nonpuerperal galactorrhea", "Milk from non-pregnant breast", "Inappropriate production of milk", "Spontaneous milk flow from breast", "nonpuerperal galactorrhea (diagnosis)", "Galactorrhea due to non-obstetric cause", "Galactorrhoea due to non-obstetric cause", "Galactorrhea not associated with childbirth", "Galactorrhoea not associated with childbirth", "galactorrhea; not associated with childbirth", "Galactorrhea due to non-obstetric cause (disorder)", "Galactorrhea not associated with childbirth (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "galactorrhea", "shortest_name_length": 12}
{"curie": "MONDO:0012094", "names": ["HPC4", "Prostate Cancer, Hereditary, 4", "prostate cancer, hereditary, 4", "PROSTATE CANCER, HEREDITARY, 4", "prostate cancer, hereditary, type 4", "prostate cancer, susceptibility to, 4", "prostate cancer, hereditary, on chromosome 7", "PROSTATE CANCER, HEREDITARY, ON CHROMOSOME 7", "Prostate Cancer, Hereditary, on Chromosome 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate cancer, hereditary, 4", "shortest_name_length": 4}
{"curie": "MONDO:0000648", "names": ["Benign neoplasms", "benign nervous system tumor", "Benign neurologic neoplasms", "Benign Nervous System Tumor", "Nervous system neoplasm benign", "Benign Tumor of Nervous System", "nervous system benign neoplasm", "Benign tumor of nervous system", "Benign Nervous System Neoplasm", "benign nervous system neoplasm", "benign tumor of nervous system", "Benign neoplasm nervous system", "Nervous system neoplasms benign", "Benign tumour of nervous system", "nervous system neoplasm, benign", "Nervous System Neoplasm, Benign", "Benign neoplasm of nervous system", "Benign Neoplasm of Nervous System", "benign neoplasm of nervous system", "benign tumor of the nervous system", "Benign nervous system neoplasm NOS", "Nervous system neoplasm benign NOS", "Benign Tumor of the Nervous System", "Benign neoplasm of nervous system NOS", "Benign Neoplasm of the Nervous System", "benign neoplasm of the nervous system", "Benign neoplasm of nervous system, NOS", "Benign neoplasm of nervous system (disorder)", "benign neoplasm of nervous system (diagnosis)", "Benign neoplasm of nervous system, part unspecified", "Benign neoplasm of brain and other parts of nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nervous system benign neoplasm", "shortest_name_length": 16}
{"curie": "MONDO:0009302", "names": ["gonadal dysgenesis XY type associated anomalies", "Gonadal dysgenesis XY type with associated anomalies", "gonadal dysgenesis, XY type, with associated anomalies", "Gonadal Dysgenesis, XY Type, with Associated Anomalies", "gonadal dysgenesis, 10Y type, with associated anomalies", "XY type gonadal dysgenesis-associated anomalies syndrome", "XY type gonadal dysgenesis with associated anomalies syndrome", "XY type gonadal dysgenesis with associated anomalies syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "XY type gonadal dysgenesis-associated anomalies syndrome", "shortest_name_length": 47}
{"curie": "MONDO:0016230", "names": ["simple vascular malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "simple vascular malformation", "shortest_name_length": 28}
{"curie": "UMLS:C4479059", "names": ["Conjunctival Keratoacanthoma", "Conjunctival keratoacanthomas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conjunctival keratoacanthomas", "shortest_name_length": 28}
{"curie": "MONDO:0008638", "names": ["varix", "Varix", "VARICES", "varices", "Varices", "Varix, NOS", "VARICOSITY", "Varicosity", "Varicosities", "phlebectasia", "Phlebectasia", "varicosities", "VARICOSE VEIN", "VEIN VARICOSE", "Varicose vein", "Vein varicose", "Varicose Vein", "varicose vein", "varicose veins", "Venous varices", "Venous ectasia", "Varicose Veins", "Varicose veins", "VARICOSE VEINS", "Vein, Varicose", "venous ectasia", "Veins, Varicose", "varicose disease", "Varicose veins NOS", "Venous varicosities", "VV - Varicose veins", "VVs - Varicose veins", "Uneven venous ectasia", "Venous varices (disorder)", "varicose veins (diagnosis)", "enlarged tortuous blood vessel", "varicose veins lower extremities", "Venous ectasia (morphologic abnormality)", "Uneven venous ectasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "varicose disease", "shortest_name_length": 5}
{"curie": "MONDO:0700180", "names": ["feline bronchioloalveolar lung carcinoma", "Feline Bronchioloalveolar Lung Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "feline bronchioloalveolar lung carcinoma", "shortest_name_length": 40}
{"curie": "UMLS:C0849867", "names": ["Extensive Disease", "Widespread Disease", "Generalized Disease", "Generalised illness", "Disease;generalised", "generalized disease", "Generalized illness", "generalised disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Generalised illness", "shortest_name_length": 17}
{"curie": "MONDO:0017178", "names": ["OD", "OCD", "SSOAOD", "Konig disease", "König disease", "Idiopathic AVN", "Koenig disease", "osteochondritis", "OSTEOCHONDRITIS", "Osteochondritis", "Osteochondritides", "Osteochondritis NOS", "Osteochondritis, NOS", "Osteochondritis;dissecans", "OSTEOCHONDRITIS DISSECANS", "Osteochondritis dissecans", "OSTEOCHONDRITIS DESSICANS", "Osteochondrosis dessicans", "Osteochondritis Dissecans", "osteochondritis dissecans", "Osteochondrosis dissecans", "osteochondrosis; dissecans", "dissecans; osteochondrosis", "Dissecans, Osteochondritis", "osteochondritis; dissecans", "Osteochondritis (disorder)", "dissecans; osteochondritis", "Idiopathic avascular necrosis", "OD - Osteochondritis dissecans", "OCD - Osteochondritis dissecans", "familial osteochondritis dissecans", "osteochondritis dissecans (disease)", "Osteochondritis dissecans (disorder)", "osteochondritis dissecans (diagnosis)", "osteochondritis dissecans and short stature", "Osteochondritis not specified as adult or juvenile, of unspecified site", "osteochondritis dissecans, short stature, and early-onset osteoarthritis", "short stature and advanced bone Age, with or without early-onset osteoarthritis and/Or osteochondritis Dissecans"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteochondritis dissecans", "shortest_name_length": 2}
{"curie": "UMLS:C0399473", "names": ["Speckled oral leucoplakia", "Speckled oral leukoplakia", "Speckled Oral Leukoplakia", "Nodular leukoplakia of oral mucosa", "Speckled oral leukoplakia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Speckled oral leukoplakia", "shortest_name_length": 25}
{"curie": "MONDO:0013345", "names": ["D2HGA2", "D-2-HYDROXYGLUTARIC ACIDURIA 2", "D-2-hydroxyglutaric aciduria 2", "d-2-hydroxyglutaric aciduria 2", "IDH2 D-2-hydroxyglutaric aciduria", "D-2-hydroxyglutaric aciduria type 2", "D-2-hydroxyglutaric aciduria caused by mutation in IDH2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "d-2-hydroxyglutaric aciduria 2", "shortest_name_length": 6}
{"curie": "UMLS:C2981672", "names": ["Stage IIA Ampulla of Vater Cancer", "Stage IIA Ampulla of Vater Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Ampulla of Vater Cancer AJCC v7", "shortest_name_length": 33}
{"curie": "UMLS:C1698098", "names": ["Intraoperative arterial injury", "intraoperative arterial injury", "Intraoperative Arterial Injury", "intraoperative arterial injury (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraoperative Arterial Injury", "shortest_name_length": 30}
{"curie": "MONDO:0019325", "names": ["phakomatosis cesioflammea", "Phakomatosis cesioflammea", "Phakomatosis cesioflammea (disorder)", "Phakomatosis pigmentovascularis type 2", "phakomatosis pigmentovascularis type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "phakomatosis cesioflammea", "shortest_name_length": 25}
{"curie": "UMLS:C1334695", "names": ["Meninges Gliomatosis", "Meningeal Gliomatosis", "Gliomatosis of Meninges", "Gliomatosis of the Meninges"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meningeal Gliomatosis", "shortest_name_length": 20}
{"curie": "UMLS:C1709540", "names": ["Piloleiomyoma", "Pilar leiomyoma", "Pilar Leiomyoma", "Pilar leiomyoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pilar Leiomyoma", "shortest_name_length": 13}
{"curie": "MONDO:0013004", "names": ["HYPOTONIA, SEIZURES, AND PRECOCIOUS PUBERTY", "hypotonia, seizures, and precocious puberty", "Hypotonia, Seizures, And Precocious Puberty"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotonia, seizures, and precocious puberty", "shortest_name_length": 43}
{"curie": "MONDO:0005005", "names": ["RCC", "CCRCC", "Grawitz Tumor", "hypernephroma", "Hypernephroma", "Grawitz tumor", "HYPERNEPHROMA", "GRAWITZ TUMOR", "Hypernephromas", "Tumor, Grawitz", "Grawitz tumour", "tumor; Grawitz", "Grawitz; tumor", "Hypernephroid tumor", "renal cell carcinoma", "HYPERNEPHROID CARCINOMA", "Hypernephroid Carcinoma", "hypernephroid carcinoma", "Hypernephroid Carcinomas", "Carcinoma, Hypernephroid", "renal cell adenocarcinoma", "clear cell renal carcinoma", "renal clear cell carcinoma", "Clear cell renal carcinoma", "Renal clear cell carcinoma", "Clear Cell Renal Carcinoma", "Renal Clear Cell Carcinoma", "kidney clear cell carcinoma", "clear cell kidney carcinoma", "Kidney Clear Cell Carcinoma", "carcinoma cell clear kidney", "Clear Cell Renal Cell Cancer", "carcinoma, clear cell, renal", "clear cell renal cell cancer", "clear cell carcinoma of kidney", "Clear Cell Carcinoma of Kidney", "RCC, clear cell adenocarcinoma", "Clear cell carcinoma of kidney", "Renal Clear Cell Adenocarcinoma", "renal clear cell adenocarcinoma", "Clear Cell Renal Cell Carcinoma", "Clear cell renal cell carcinoma", "clear cell renal cell carcinoma", "kidney clear cell adenocarcinoma", "Kidney Clear Cell Adenocarcinoma", "RENAL CELL CARCINOMA, CLEAR CELL", "Nonpapillary renal cell carcinoma", "Clear Cell Adenocarcinoma, Kidney", "clear cell adenocarcinoma, kidney", "conventional renal cell carcinoma", "Conventional Renal Cell Carcinoma", "Clear cell carcinoma of the kidney", "Clear Cell Carcinoma of the Kidney", "clear cell carcinoma of the kidney", "RENAL CELL CARCINOMA, NONPAPILLARY", "clear cell adenocarcinoma of kidney", "Clear Cell Adenocarcinoma of Kidney", "kidney cancer, clear cell carcinoma", "Clear cell renal cell adenocarcinoma", "renal malignant carcinoma clear cell", "Clear Cell Adenocarcinoma of the Kidney", "clear cell adenocarcinoma of the kidney", "Clear cell carcinoma of kidney (disorder)", "Clear-cell metastatic renal cell carcinoma", "clear-cell metastatic renal cell carcinoma", "Clear cell carcinoma of kidney (diagnosis)", "conventional (clear cell) renal cell carcinoma", "conventional (Clear cell) renal cell carcinoma", "Conventional (Clear Cell) Renal Cell Carcinoma", "clear cell adenocarcinoma of kidney (diagnosis)", "renal cell carcinoma, clear cell adenocarcinoma", "Renal cell carcinoma, clear cell adenocarcinoma", "Conventional (Clear Cell) Renal Cell Adenocarcinoma", "conventional (clear cell) renal cell adenocarcinoma", "Clear cell renal cell carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "clear cell renal carcinoma", "shortest_name_length": 3}
{"curie": "MONDO:0008285", "names": ["GISTPS", "GIST-PLUS SYNDROME", "Polyps, Multiple And Recurrent Inflammatory Fibroid, Gastrointestinal", "polyps, multiple and recurrent inflammatory fibroid, gastrointestinal", "gastrointestinal stromal tumor/GIST-plus syndrome, somatic or familial", "POLYPS, MULTIPLE AND RECURRENT INFLAMMATORY FIBROID, GASTROINTESTINAL, FORMERLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyps, multiple and recurrent inflammatory fibroid, gastrointestinal", "shortest_name_length": 6}
{"curie": "UMLS:C5237305", "names": ["Refractory Differentiated Thyroid Gland Carcinoma", "Refractory Follicular/Papillary Thyroid Gland Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Differentiated Thyroid Gland Carcinoma", "shortest_name_length": 49}
{"curie": "UMLS:C0919702", "names": ["Ventricular hypokinesia", "ventricular hypokinesia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ventricular hypokinesia", "shortest_name_length": 23}
{"curie": "MONDO:0800042", "names": ["RSDM1", "Restrictive dermopathy", "restrictive dermopathy", "RESTRICTIVE DERMOPATHY 1", "restrictive dermopathy 1", "lethal restrictive dermopathy", "Lethal restrictive dermopathy", "restrictive dermopathy, lethal", "Restrictive dermopathy, lethal", "tight skin contracture syndrome", "restrictive dermopathy 1, lethal", "RESTRICTIVE DERMOPATHY 1, LETHAL", "Infantile restrictive dermopathy", "hyperkeratosis-contracture syndrome", "HYPERKERATOSIS-CONTRACTURE SYNDROME", "Hyperkeratosis-contracture syndrome", "Lethal tight skin contracture syndrome", "Lethal tight skin-contracture syndrome", "Tight skin contracture syndrome, lethal", "TIGHT SKIN CONTRACTURE SYNDROME, LETHAL", "tight skin contracture syndrome, lethal", "Lethal hyperkeratosis-contracture syndrome", "Lethal tight skin contracture syndrome (disorder)", "FETAL HYPOKINESIA SEQUENCE DUE TO RESTRICTIVE DERMOPATHY", "fetal hypokinesia sequence due to restrictive dermopathy", "Fetal hypokinesia sequence due to restrictive dermopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "restrictive dermopathy 1", "shortest_name_length": 5}
{"curie": "UMLS:C4744398", "names": ["Recurrent Endometrial Clear Cell Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Endometrial Clear Cell Adenocarcinoma", "shortest_name_length": 47}
{"curie": "MONDO:0000612", "names": ["lymphatic system cancer", "lymphatic part of lymphoid system cancer", "cancer of lymphatic part of lymphoid system", "malignant lymphatic part of lymphoid system neoplasm", "malignant neoplasm of lymphatic part of lymphoid system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphatic system cancer", "shortest_name_length": 23}
{"curie": "UMLS:C0023223", "names": ["Ulcer;leg", "leg ulcer", "Leg Ulcer", "Leg ulcer", "Ulcer, Leg", "leg ulcers", "Leg Ulcers", "Ulcers, Leg", "Leg--Ulcers", "Leg(s) Ulcer(s)", "Ulcer of leg, NOS", "ulcer; lower limb", "lower limb; ulcer", "Ulcer of lower limb", "LOWER EXTREMITY ULCER", "lower extremity ulcer", "Lower Extremity Ulcer", "Lower extremity ulcers", "Ulcer of lower extremity", "LOWER EXTREMITY ULCERATION", "ulcer of lower extremities", "ulcers of lower extremities", "Lower extremities ulcers of", "Ulcer of lower extremity (disorder)", "ulcer of lower extremities (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leg Ulcer", "shortest_name_length": 9}
{"curie": "MONDO:0013269", "names": ["DFNB91", "autosomal recessive deafness 91", "DEAFNESS, AUTOSOMAL RECESSIVE 91", "deafness, autosomal recessive 91", "deafness, autosomal recessive type 91", "autosomal recessive nonsyndromic deafness 91", "autosomal recessive nonsyndromic hearing loss 91", "autosomal recessive nonsyndromic deafness type 91", "SERPINB6 autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic deafness caused by mutation in SERPINB6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 91", "shortest_name_length": 6}
{"curie": "UMLS:C0948221", "names": ["pyelocaliectasis", "Pyelocaliectasis", "Pyelocaliectasis NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pyelocaliectasis", "shortest_name_length": 16}
{"curie": "UMLS:C0855002", "names": ["Recurrent Lung Cancer", "Recurrent Lung Carcinoma", "Lung carcinoma recurrent", "Pulmonary carcinoma recurrent", "Relapsed Unspecified Lung Carcinoma", "Recurrent Unspecified Lung Carcinoma", "Relapsed Unspecified Carcinoma of Lung", "Recurrent Unspecified Carcinoma of Lung", "Relapsed Unspecified Carcinoma of the Lung", "Recurrent Unspecified Carcinoma of the Lung", "Lung carcinoma cell type unspecified recurrent", "Pulmonary carcinoma cell type unspecified recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Unspecified Lung Carcinoma", "shortest_name_length": 21}
{"curie": "UMLS:C4330668", "names": ["Not Determined", "Medulloblastoma, NOS", "Medulloblastoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Medulloblastoma, Not Otherwise Specified", "shortest_name_length": 14}
{"curie": "MONDO:0003537", "names": ["T Lymphoblastic Leukemia/Lymphoma", "T-Lymphoblastic Leukemia/Lymphoma", "T-lymphoblastic lymphoma/leukemia", "T lymphoblastic leukemia/lymphoma", "T lymphoblastic leukaemia/lymphoma", "T-lymphoblastic lymphoma/leukaemia", "T-cell lymphoblastic leukemia/lymphoma", "T-Cell Lymphoblastic Leukemia/Lymphoma", "precursor T lymphoblastic lymphoma/leukemia", "Precursor T-lymphoblastic lymphoma/leukemia", "Precursor T Lymphoblastic Leukemia/Lymphoma", "Precursor T Lymphoblastic Lymphoma/Leukemia", "Precursor T-Lymphoblastic Lymphoma/Leukemia", "precursor T-lymphoblastic lymphoma/leukemia", "precursor T lymphoblastic leukemia/lymphoma", "Precursor T-lymphoblastic lymphoma/leukaemia", "Precursor T-lymphoblastic lymphomas/leukemias", "Precursor T-lymphoblastic lymphomas/leukaemias", "Precursor T-lymphoblastic lymphoma/leukemia NOS", "Precursor T-lymphoblastic lymphoma/leukaemia NOS", "T lymphoblastic leukemia/lymphoma (morphologic abnormality)", "malignant precursor T-cell lymphoblastic leukemia or lymphoma", "Precursor T cell lymphoblastic leukemia/lymphoblastic lymphoma", "malignant precursor T-cell lymphoblastic leukemia or lymphoma (diagnosis)", "Precursor T cell lymphoblastic leukemia/lymphoblastic lymphoma (disorder)", "Precursor T cell lymphoblastic leukemia/lymphoblastic lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "precursor T-lymphoblastic lymphoma/leukemia", "shortest_name_length": 33}
{"curie": "MONDO:0005293", "names": ["Flatfeet", "Flatfoot", "flatfoot", "flatfeet", "FLATFOOT", "Flat Foot", "Flat Feet", "Flat feet", "Splayfoot", "flat foot", "flat Foot", "feet flat", "Flat foot", "flat feet", "pes valgus", "Pes planus", "Pes Planus", "Foot, Flat", "Feet, Flat", "pes planus", "Pes valgus", "pes; planus", "planus; pes", "Fallen arch", "fallen Arch", "Fallen Arch", "fallen arch", "flat footed", "fallen arche", "arches; weak", "weak; arches", "fallen arches", "arches fallen", "Fallen arches", "talipes planus", "Talipes planus", "Talipes Valgus", "Dropped arches", "Valgus, Talipes", "talipes; planus", "pes planovalgus", "planus; talipes", "Pes planovalgus", "depressed; arches", "depression; arches", "arches; depression", "Acquired flat foot", "acquired flat foot", "Acquired pes planus", "Pes planus (flat foot)", "pes planus (flat foot)", "Low medial arch of foot", "Acquired talipes planus", "low medial arch of foot", "fallen arches were noted", "Talipes planus (disorder)", "feet medial fallen arches", "feet pes planus (flatfoot)", "pes planus (physical finding)", "Acquired pes planus (disorder)", "Acquired pes planus (diagnosis)", "Flat foot [pes planus] (acquired)", "low medial arch of foot (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "flatfoot", "shortest_name_length": 8}
{"curie": "MONDO:0030856", "names": ["DEE89", "early infantile epileptic encephalopathy 89", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 89", "developmental and epileptic encephalopathy 89"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy 89", "shortest_name_length": 5}
{"curie": "MONDO:0011010", "names": ["PMD", "PDAC", "MCOPS9", "MCOPCB8", "PDAC syndrome", "Spear Syndrome", "Spear syndrome", "SPEAR SYNDROME", "spear syndrome", "Matthew Wood syndrome", "MATTHEW-WOOD SYNDROME", "Matthew-Wood syndrome", "syndromic microphthalmia 9", "microphthalmia syndromic 9", "Microphthalmia, Syndromic 9", "microphthalmia, syndromic 9", "MICROPHTHALMIA, SYNDROMIC 9", "Syndromic microphthalmia type 9", "syndromic microphthalmia type 9", "microphthalmia syndromic type 9", "Matthew Wood syndrome (disorder)", "microphthalmia, syndromic type 9", "ANOPHTHALMIA AND PULMONARY HYPOPLASIA", "Anophthalmia with pulmonary hypoplasia", "MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 8", "microphthalmia, isolated, with coloboma 8", "Anophthalmia-pulmonary hypoplasia syndrome", "anophthalmia-pulmonary hypoplasia syndrome", "Anophthalmia with pulmonary hypoplasia syndrome", "anophthalmia/microphthalmia and pulmonary hypoplasia", "Anophthalmia-Microphthalmia And Pulmonary Hypoplasia", "ANOPHTHALMIA/MICROPHTHALMIA AND PULMONARY HYPOPLASIA", "pulmonary agenesis microphthalmi and diaphragmatic defect", "PULMONARY AGENESIS, MICROPHTHALMIA, AND DIAPHRAGMATIC DEFECT", "Pulmonary agenesis, Microphthalmia, and Diaphragmatic defect", "pulmonary agenesis, microphthalmia, and diaphragmatic defect", "pulmonary Hypoplasia-diaphragmatic hernia-anophthalmia-Cardiac defect", "PULMONARY HYPOPLASIA-DIAPHRAGMATIC HERNIA-ANOPHTHALMIA-CARDIAC DEFECT", "Pulmonary hypoplasia-diaphragmatic hernia-anophthalmia-cardiac defect syndrome", "clinical anophthalmia mild facial dysmorphism lung heart and diaphragm malformations", "anophthalmia, clinical, with mild Facial Dysmorphism and variable malformations of the lung, heart, and diaphragm", "ANOPHTHALMIA, CLINICAL, WITH MILD FACIAL DYSMORPHISM AND VARIABLE MALFORMATIONS OF THE LUNG, HEART, AND DIAPHRAGM", "Anophthalmia, Clinical, With Mild Facial Dysmorphism And Variable Malformations Of The Lung, Heart, And Diaphragm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Matthew-Wood syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0011687", "names": ["Cmt2f", "CMT2F", "CMT 2F", "Charcot Marie Tooth disease type 2F", "Charcot-Marie-Tooth disease type 2F", "Charcot-Marie-Tooth disease, Type 2F", "Charcot-Marie-Tooth neuronal type 2F", "Charcot-Marie-Tooth neuropathy type 2F", "Charcot-Marie-Tooth neuropathy, type 2F", "Charcot-Marie-Tooth Neuropathy, Type 2f", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2F", "HSPB1 Charcot-Marie-Tooth disease type 2", "Charcot-Marie-Tooth disease axonal type 2F", "Charcot-Marie-Tooth disease, axonal, Type 2F", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F", "Charcot-Marie-Tooth disease, axonal, type 2F", "Charcot-Marie-Tooth disease, neuronal, Type 2F", "CHARCOT-MARIE-TOOTH DISEASE, NEURONAL, TYPE 2F", "Charcot-Marie-Tooth disease, neuronal, type 2F", "Charcot-Marie-Tooth disease type 2F (diagnosis)", "Autosomal dominant Charcot-Marie-Tooth disease type 2F", "autosomal dominant Charcot-Marie-Tooth disease type 2F", "Charcot-Marie-Tooth disease type 2 caused by mutation in HSPB1", "Autosomal dominant Charcot-Marie-Tooth disease type 2F (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease axonal type 2F", "shortest_name_length": 5}
{"curie": "MONDO:0008300", "names": ["PWS", "PWCR", "H2O syndrome", "Prader-Willi", "PRADER-WILLI SYNDROME", "prader syndrome willy", "syndrome willi prader", "PRADER WILLI SYNDROME", "prader syndrome willi", "Prader Willi Syndrome", "Willi Prader Syndrome", "prader willi syndrome", "Prader-Willi syndrome", "prader willy syndrome", "willi prader syndrome", "Willi-Prader Syndrome", "syndrome prader-willi", "Willi-Prader syndrome", "prader-willi syndrome", "Prader-Willi Syndrome", "Prader Willi syndrome", "prader willi syndromes", "Syndrome, Prader-Willi", "Syndrome, Willi-Prader", "Labhart Willi Syndrome", "Labhart-Willi Syndrome", "prader willis syndrome", "prader syndrome willis", "Syndrome, Labhart-Willi", "prader willies syndrome", "prader syndrome willies", "Prader-Willi syndrome (PWS)", "Prader-Willi-Labhart Syndrome", "Prader Labhart Willi syndrome", "Prader-Labhart-Willi syndrome", "PRADER-LABHART-WILLI SYNDROME", "Prader-Willi-Labhart syndrome", "Prader-Labhart-Willi Syndrome", "Prader Labhart Willi Syndrome", "Syndrome, Prader-Labhart-Willi", "Prader-Willi syndrome (disorder)", "Prader-Willi syndrome (diagnosis)", "Labhart Willi Prader Fanconi Syndrome", "Prader-Labhart-Willi-Fanconi syndrome", "Labhart-Willi-Prader-Fanconi Syndrome", "Syndrome, Labhart-Willi-Prader-Fanconi", "hypotonia-hypogonadism-obesity syndrome", "Prader-Willi syndrome chromosome region", "PRADER-WILLI SYNDROME CHROMOSOME REGION", "Prader-Labhart-Willi (PLW) syndrome (PLWS)", "cardiorespiratory syndrome of obesity in child", "hypogenital dystrophy with diabetic tendency syndrome", "hypotonia-hypopigmentia-hypogonadism-obesity syndrome", "PRADER-WILLI-LIKE SYNDROME ASSOCIATED WITH CHROMOSOME 6", "Prader-Willi-like syndrome associated with chromosome 6", "Prader-Willi-Like Syndrome Associated With Chromosome 6", "hypotonia-obesity-hypogonadism-mental retardation syndrome", "OBESITY-CRYPTORCHIDISM-DWARFISM-SUBNORMAL MENTALITY SYNDROME", "hypotonia-hypopigmentia-hypogonadism-obesity (HHHO) syndrome", "obesity, muscular hypotonia, mental retardation, short stature, hypogonadotropic hypogonadism, and small hands and feet", "obesity, muscular hypotonia, intellectual disability, short stature, hypogonadotropic hypogonadism, and small hands and feet"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prader-Willi syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0023557", "names": ["Vaginitis NOS", "Vaginal Infection", "Infection;vaginal", "VAGINAL INFECTION", "vaginal infection", "infection; vagina", "Vaginal infection", "vagina; infection", "Vaginal Infections", "vaginitis infective", "infective vaginitis", "Infective vaginitis", "Vaginal infection NOS", "PV - Vaginal infection", "Infective vaginitis (disorder)", "infective vaginitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infective vaginitis", "shortest_name_length": 13}
{"curie": "MONDO:0023020", "names": ["dwarfism deafness retinitis pigmentosa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dwarfism deafness retinitis pigmentosa", "shortest_name_length": 38}
{"curie": "MONDO:0004567", "names": ["ileus", "ILEUS", "Ileus", "Ileus, NOS", "bowel ileus", "Ileus of bowel", "ileus (diagnosis)", "ileus of intestine", "Ileus of intestine", "Non-mechanical ileus", "Gastrointestinal atony", "intestinal obstruction due to decreased peristalsis", "bowel obstruction causing colic, vomiting, and constipation", "intestinal obstruction due to decreased peristalsis (diagnosis)", "Intestinal obstruction co-occurrent and due to decreased peristalsis", "Intestinal obstruction co-occurrent and due to decreased peristalsis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ileus", "shortest_name_length": 5}
{"curie": "MONDO:0002183", "names": ["enthesopathy", "Enthesopathy", "enthesopathies", "Enthesopathies", "enthesis disease", "disease of enthesis", "disorder of enthesis", "Enthesopathy (disorder)", "unspecified enthesopathy", "Unspecified enthesopathy", "enthesopathy (diagnosis)", "Enthesopathy, unspecified", "enthesis disease or disorder", "Enthesopathy of specified site", "muscular; disease, attachments", "disease or disorder of enthesis", "Enthesopathy of unspecified site", "Enthesopathy of unspecified site, NOS", "ligament; disorder ligamentous attachments"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "enthesopathy", "shortest_name_length": 12}
{"curie": "MONDO:0009467", "names": ["Natal teeth, intestinal pseudoobstruction and patent ductus", "natal teeth-intestinal pseudoobstruction-patent ductus syndrome", "INTESTINAL PSEUDOOBSTRUCTION WITH PATENT DUCTUS ARTERIOSUS AND NATAL TEETH", "intestinal pseudoobstruction with patent ductus arteriosus and NATAL teeth", "Intestinal Pseudoobstruction with Patent Ductus Arteriosus and Natal Teeth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "natal teeth-intestinal pseudoobstruction-patent ductus syndrome", "shortest_name_length": 59}
{"curie": "MONDO:0018056", "names": ["lichen planus bullous", "bullous lichen planus", "Bullous lichen planus", "Bullous Lichen Planus", "Lichen planus, bullous", "Lichen planus bullosus", "lichen; planus, bullous", "Bullous lichen planus (disorder)", "bullous lichen planus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bullous lichen planus", "shortest_name_length": 21}
{"curie": "MONDO:0015599", "names": ["atopic keratoconjunctivitis", "Atopic keratoconjunctivitis", "Atopic keratoconjunctivitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atopic keratoconjunctivitis", "shortest_name_length": 27}
{"curie": "MONDO:0005808", "names": ["Trachoma", "paratrachoma", "Paratrachoma", "Inclusion blenorrhea", "inclusion blenorrhea", "Inclusion blennorrhea", "Inclusion blenorrhoea", "Inclusion Blennorrhea", "Inclusion Blennorrheas", "inclusion blennorrhoea", "Inclusion blennorrhoea", "Blennorrhea, Inclusion", "Blennorrheas, Inclusion", "conjunctivitis chlamydia", "Inclusion conjunctivitis", "chlamydia conjunctivitis", "Inclusion Conjunctivitis", "inclusion conjunctivitis", "paratrachoma (diagnosis)", "INCLUSION CONJUNCTIVITIS", "conjunctivitis inclusion", "Conjunctivitis;chlamydia", "Conjunctivitis, Inclusion", "CONJUNCTIVITIS, CHLAMYDIA", "Conjunctivitis chlamydial", "Chlamydial Conjunctivitis", "Chlamydial conjunctivitis", "chlamydial conjunctivitis", "CONJUNCTIVITIS, INCLUSION", "Inclusion Conjunctivitides", "Conjunctivitides, Inclusion", "swimming pool conjunctivitis", "Swimming-pool conjunctivitis", "Swimming pool conjunctivitis", "adult inclusion conjunctivitis", "Neonatal inclusion blennorrhea", "ADULT INCLUSION CONJUNCTIVITIS", "Chlamydial ophthalmia neonatorum", "Chlamydia conjunctivitis neonatal", "neonatal Chlamydia conjunctivitis", "Neonatal Chlamydia Conjunctivitis", "Ophthalmia neonatorum - chlamydial", "Neonatal chlamydial conjunctivitis", "Chlamydia; conjunctivitis, neonatal", "conjunctivitis; Chlamydia, neonatal", "Chlamydial conjunctivitis (disorder)", "inclusion conjunctivitis (diagnosis)", "Adult chlamydial keratoconjunctivitis", "Inclusion conjunctivitis of the adult", "Neonatal inclusion body conjunctivitis", "swimming pool conjunctivitis (diagnosis)", "Neonatal conjunctivitis due to chlamydiae", "Neonatal chlamydial conjunctivitis (disorder)", "Inclusion conjunctivitis of the adult (disorder)", "Chronic conjunctivitis due to Chlamydia trachomatis", "Inclusion conjunctivitis due to Chlamydia trachomatis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inclusion conjunctivitis", "shortest_name_length": 8}
{"curie": "UMLS:C1516416", "names": ["Cervical Glandular Tumor", "Cervical Glandular Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Glandular Neoplasm", "shortest_name_length": 24}
{"curie": "MONDO:0030881", "names": ["DEE102", "early infantile epileptic encephalopathy 102", "developmental and epileptic encephalopathy 102", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 102"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy 102", "shortest_name_length": 6}
{"curie": "MONDO:0016040", "names": ["Harlequin syndrome", "harlequin syndrome", "Harlequin syndrome (disorder)", "harlequin syndrome (diagnosis)", "progressive isolated segmental anhidrosis", "Progressive isolated segmental anhidrosis", "Sudden onset of unilateral flushing and sweating", "sudden onset of unilateral flushing and sweating", "unilateral loss of facial flushing and sweating with contralateral anhidrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "harlequin syndrome", "shortest_name_length": 18}
{"curie": "UMLS:C4288749", "names": ["Micropapillary carcinoma, NOS", "Micropapillary adenocarcinoma", "Lung Micropapillary Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Micropapillary Adenocarcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0030998", "names": ["DFNA80", "deafness, autosomal dominant 80", "DEAFNESS, AUTOSOMAL DOMINANT 80", "hearing loss, autosomal dominant 80"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal dominant 80", "shortest_name_length": 6}
{"curie": "UMLS:C1367539", "names": ["Giant Cell Angiofibroma", "Giant cell angiofibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Giant Cell Angiofibroma", "shortest_name_length": 23}
{"curie": "UMLS:C1336268", "names": ["Stage III Retinoblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Retinoblastoma", "shortest_name_length": 24}
{"curie": "UMLS:C0852110", "names": ["Lower respiratory tract infection viral", "Viral lower respiratory tract infections"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lower respiratory tract infection viral", "shortest_name_length": 39}
{"curie": "UMLS:C4525122", "names": ["Stage IIA Colon Cancer", "Stage IIA Colon Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Colon Cancer AJCC v8", "shortest_name_length": 22}
{"curie": "MONDO:0011849", "names": ["PSORIATIC ARTHRITIS", "Psoriatic arthritis", "Psoriatic Arthritis", "Arthritis;psoriatic", "psoriatic arthritis", "ARTHRITIS PSORIATIC", "arthritic psoriasis", "arthritis psoriatic", "Arthritic Psoriasis", "ARTHRITIS, PSORIATIC", "Arthritis, Psoriatic", "arthritis psoriatics", "arthritis psoriatica", "Arthritis Psoriatica", "Psoriasis, Arthritic", "Arthritis, psoriatic", "psoriatic arthropathy", "Psoriatic arthropathy", "psoriasis arthropathy", "Arthropathy;psoriatic", "Psoriatic Arthropathy", "Arthropathy psoriatic", "arthropathic psoriasis", "psoriasis arthropathic", "Arthropathy, Psoriatic", "Arthropathic psoriasis", "psoriasis arthropathica", "Psoriatic Arthropathies", "Psoriasis Arthropathica", "Psoriatic arthropathies", "PSORIASIS, ARTHROPATHIC", "Arthropathies, Psoriatic", "PA - Psoriatic arthritis", "PA (Psoriatic arthritis)", "PsA - Psoriatic arthritis", "PsA (Psoriatic arthritis)", "Psoriasis with arthropathy", "Psoriatic arthritis (disorder)", "psoriatic arthropathy (diagnosis)", "arthropathic; psoriasis (etiology)", "arthropathic psoriasis (diagnosis)", "psoriasis; arthropathic (etiology)", "Arthropathic psoriasis, unspecified", "susceptibility to psoriatic arthritis", "psoriatic arthritis, susceptibility to", "arthropathic; psoriasis (manifestation)", "psoriasis; arthropathic (manifestation)", "psoriatic arthritis, susceptibility to, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "psoriatic arthritis", "shortest_name_length": 19}
{"curie": "MONDO:0002576", "names": ["Extrahepatic Bile Duct Embryonal Rhabdomyosarcoma", "extrahepatic bile duct embryonal rhabdomyosarcoma", "embryonal extrahepatic bile duct rhabdomyosarcoma", "Embryonal Extrahepatic Bile Duct Rhabdomyosarcoma", "embryonal rhabdomyosarcoma of extrahepatic bile duct", "Embryonal Rhabdomyosarcoma of Extrahepatic Bile Duct", "embryonal rhabdomyosarcoma of the extrahepatic bile duct", "Embryonal Rhabdomyosarcoma of the Extrahepatic Bile Duct", "extrahepatic bile duct embryonal rhabdomyosarcoma (disease)", "embryonal rhabdomyosarcoma (disease) of extrahepatic bile duct"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "embryonal extrahepatic bile duct rhabdomyosarcoma", "shortest_name_length": 49}
{"curie": "MONDO:0014232", "names": ["CRS5", "ALX4 craniosynostosis", "susceptibility to craniosynostosis 5", "CRANIOSYNOSTOSIS 5, SUSCEPTIBILITY TO", "craniosynostosis 5, susceptibility to", "craniosynostosis caused by mutation in ALX4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniosynostosis 5, susceptibility to", "shortest_name_length": 4}
{"curie": "MONDO:0011921", "names": ["CAA", "Congenital aural atresia", "aural atresia, congenital", "Aural Atresia, Congenital", "AURAL ATRESIA, CONGENITAL", "AURAL ATRESIA, CONGENITAL, WITH HYPOSMIA", "aural atresia, congenital, with hyposmia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aural atresia, congenital", "shortest_name_length": 3}
{"curie": "UMLS:C2983572", "names": ["Vaginal Cancer by AJCC v6 Stage", "Vaginal Carcinoma by AJCC v6 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Cancer by AJCC v6 Stage", "shortest_name_length": 31}
{"curie": "MONDO:0010661", "names": ["GUST", "gust", "GUSTAVSON SYNDROME", "Gustavson syndrome", "X-linked mental retardation Gustavson type", "X-linked intellectual disability Gustavson type", "Mental retardation X-linked severe Gustavson type", "mental retardation X-linked severe Gustavson type", "Severe X-linked intellectual disability Gustavson type", "intellectual disability X-linked severe Gustavson type", "severe X-linked intellectual disability, Gustavson type", "Severe X-linked intellectual disability, Gustavson type", "mental retardation-optic atrophy-deafness-seizures syndrome", "mental retardation with optic atrophy, deafness and seizures", "Mental retardation with optic atrophy, deafness, and seizures", "MENTAL RETARDATION WITH OPTIC ATROPHY, DEAFNESS, AND SEIZURES", "mental retardation with optic atrophy, deafness, and seizures", "Severe X-linked intellectual disability Gustavson type (disorder)", "intellectual disability with optic atrophy, deafness, and seizures", "severe X-linked intellectual disability, Gustavson type (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe X-linked intellectual disability, Gustavson type", "shortest_name_length": 4}
{"curie": "UMLS:C1882103", "names": ["Non-Congenital Amegakaryocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Congenital Amegakaryocytosis", "shortest_name_length": 32}
{"curie": "MONDO:0014658", "names": ["SADDAN", "SADDANs", "SADDAN DYSPLASIA", "SADDAN dysplasia", "SADDAN Dysplasia", "Dysplasia, SADDAN", "SADDAN Dysplasias", "Dysplasias, SADDAN", "Skeleton Skin Brain Syndrome", "Skeleton-Skin-Brain Syndrome", "Skeleton-Skin-Brain Syndromes", "Syndrome, Skeleton-Skin-Brain", "Syndromes, Skeleton-Skin-Brain", "severe achondroplasia-developmental delay-acanthosis nigricans syndrome", "Severe achondroplasia-developmental delay-acanthosis nigricans syndrome", "Severe achondroplasia with developmental delay and acanthosis nigricans", "severe achondroplasia with developmental delay and acanthosis nigricans", "Severe Achondroplasia with Developmental Delay and Acanthosis Nigricans", "achondroplasia, severe, with developmental delay and acanthosis nigricans", "ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS", "Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe achondroplasia-developmental delay-acanthosis nigricans syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C4763393", "names": ["Recurrent PVRL DLBCL", "Recurrent Primary Vitreoretinal Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Primary Vitreoretinal Diffuse Large B-Cell Lymphoma", "shortest_name_length": 20}
{"curie": "MONDO:0007776", "names": ["Hypersensitivity pneumonitis familial", "Familial hypersensitivity pneumonitis", "HYPERSENSITIVITY PNEUMONITIS, FAMILIAL", "hypersensitivity pneumonitis, familial", "Hypersensitivity Pneumonitis, Familial", "hereditary hypersensitivity pneumonitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypersensitivity pneumonitis, familial", "shortest_name_length": 37}
{"curie": "MONDO:0023910", "names": ["Martsolf syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Martsolf syndrome", "shortest_name_length": 17}
{"curie": "MONDO:0042601", "names": ["Samson Gardner syndrome", "Samson-Gardner syndrome", "craniosynostosis, microcephaly, hydrancephaly, humero-radial synostosis, and thumb aplasia", "Craniosynostosis, microcephaly, hydrancephaly, humero-radial synostosis, and thumb aplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Samson-Gardner syndrome", "shortest_name_length": 23}
{"curie": "MONDO:0015586", "names": ["benign FMTLE", "benign familial mesial temporal lobe epilepsy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign familial mesial temporal lobe epilepsy", "shortest_name_length": 12}
{"curie": "MONDO:0005557", "names": ["calcium metabolic disease", "calcium metabolism disease", "CALCIUM METABOLISM DISORDER", "calcium metabolism disorder", "Calcium Metabolism Disorder", "metabolic disorder; calcium", "Calcium metabolism disorder", "calcium; metabolic disorder", "Calcium Metabolism Disorders", "calcium metabolism disorders", "Calcium metabolism disorders", "Disorder, Calcium Metabolism", "Disorders, Calcium Metabolism", "Calcium--Metabolism--Disorders", "disorder of calcium metabolism", "Disorder of calcium metabolism", "disorders of calcium metabolism", "Disorders of calcium metabolism", "Disorder of calcium metabolism, NOS", "Disorder of calcium metabolism (disorder)", "Unspecified disorder of calcium metabolism", "disorders of calcium metabolism (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "calcium metabolic disease", "shortest_name_length": 25}
{"curie": "UMLS:C0919881", "names": ["ACE Fetopathy", "ACE Inhibitor Fetopathy", "ACE inhibitor fetopathy", "ACE inhibitor foetopathy", "Angiotensin Converting Enzyme Inhibitor Fetopathy", "Angiotensin converting enzyme inhibitor fetopathy", "Angiotensin converting enzyme inhibitor foetopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Angiotensin converting enzyme inhibitor foetopathy", "shortest_name_length": 13}
{"curie": "UMLS:C2033294", "names": ["papillary squamous cell carcinoma of larynx", "Laryngeal Papillary Squamous Cell Carcinoma", "Papillary squamous cell carcinoma of larynx", "Papillary squamous cell carcinoma of larynx (disorder)", "papillary squamous cell carcinoma of larynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papillary squamous cell carcinoma of larynx", "shortest_name_length": 43}
{"curie": "UMLS:C5555683", "names": ["Refractory B Acute Lymphoblastic Leukemia with t(9;22)(q34.1;q11.2); BCR-ABL1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory B Acute Lymphoblastic Leukemia with t(9;22)(q34.1;q11.2); BCR-ABL1", "shortest_name_length": 77}
{"curie": "UMLS:C1336181", "names": ["stage IIB esophageal cancer", "esophageal cancer stage IIB", "Stage IIB Esophageal Cancer", "Esophageal Cancer Stage IIB", "Stage IIB Esophagus Carcinoma", "stage IIB esophagus carcinoma", "Stage IIB Esophageal Carcinoma", "stage IIB esophageal carcinoma", "Stage IIB Carcinoma of Esophagus", "stage IIB carcinoma of esophagus", "stage IIB esophageal cancer AJCC v7", "Stage IIB Esophageal Cancer AJCC v7", "stage IIB carcinoma of the esophagus", "Stage IIB Carcinoma of the Esophagus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Esophageal Carcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0010198", "names": ["Korsakov", "korsakoff disease", "KORSAKOFF DISEASE", "Korsakoff Syndrome", "Korsakoff syndrome", "Korsakov psychosis", "DEMENTIA KORSAKOFF", "korsakoff syndrome", "korsakov psychosis", "korsakoffs syndrome", "Korsakoff Psychosis", "Korsakoff's disease", "Korsakov; psychosis", "korsakoff psychoses", "korsakoff psychosis", "korsakoff's disease", "korsakov's syndrome", "Korsakoff Psychoses", "Korsakoff psychosis", "KORSAKOFF PSYCHOSIS", "Korsakov's syndrome", "Korsakov's psychosis", "TRANSKETOLASE DEFECT", "Psychosis, Korsakoff", "Transketolase defect", "korsakoffs psychosis", "Korsakoffs Psychosis", "transketolase defect", "korsakoff's syndrome", "Korsakoff's syndrome", "Psychoses, Korsakoff", "Korsakoff's Psychosis", "Korsakoff's psychosis", "KORSAKOFF'S PSYCHOSIS", "korsakoff's psychosis", "polyneuritic psychosis", "Wernicke Encephalopathy", "psychosis polyneuritica", "Wernicke encephalopathy", "alcohol; encephalopathy", "ENCEPHALOPATHY ALCOHOLIC", "Alcoholic encephalopathy", "alcoholic encephalopathy", "encephalopathy; alcoholic", "Wernicke-Korsakov syndrome", "wernicke-korsakov syndrome", "Wernicke Korsakoff syndrome", "Wernicke-Korsakoff syndrome", "wernicke korsakoff syndrome", "Wernicke-Korsakoff Syndrome", "syndrome wernicke-korsakoff", "korsakoff syndrome wernicke", "wernicke-korsakoff syndrome", "WERNICKE-KORSAKOFF SYNDROME", "WERNICKE KORSAKOFF SYNDROME", "Wernicke Korsakoff Syndrome", "Wernicke-Korsakoff Syndromes", "Wernicke-Korsakoff psychosis", "Korsakoff's amnesic syndrome", "alcohol-induced encephalopathy", "ALCOHOL-INDUCED ENCEPHALOPATHY", "Alcohol induced encephalopathy", "Korsakoff's psychosis (disorder)", "Korsakoff's psychosis, alcoholic", "Korsakoff's psychosis (diagnosis)", "Alcoholic encephalopathy (disorder)", "Amnestic syndrome of Wernicke's disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Wernicke-Korsakoff syndrome", "shortest_name_length": 8}
{"curie": "UMLS:C1336375", "names": ["Stage IVB Larynx Verrucous Carcinoma", "Stage IVB Laryngeal Verrucous Carcinoma", "Stage IVB Verrucous Carcinoma of Larynx", "Stage IVB Laryngeal Throat Verrucous Cancer", "Stage IVB Verrucous Carcinoma of the Larynx", "Stage IVB Laryngeal Verrucous Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Laryngeal Verrucous Carcinoma AJCC v7", "shortest_name_length": 36}
{"curie": "MONDO:0003463", "names": ["Endometrioid adenoma, NOS", "Ovarian Endometrioid Adenofibroma", "ovarian endometrioid adenofibroma", "endometrioid adenofibroma of ovary", "endometrioid adenofibroma of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian endometrioid adenofibroma", "shortest_name_length": 25}
{"curie": "UMLS:C0400847", "names": ["Stenosis ileum", "STENOSIS ILEUM", "Ileal Stenosis", "Ileal stenosis", "ileum; stenosis", "Ileal stricture", "stenosis; ileum", "ileum; stricture", "Ileal strictures", "stricture; ileum", "Stenosis of ileum", "stenosis of ileum", "STENOSIS OF ILEUM", "Stricture of ileum", "Stenosis of ileum (disorder)", "stenosis of ileum (diagnosis)", "Stricture of ileum (disorder)", "stenosis of small intestine ileum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ileal Stenosis", "shortest_name_length": 14}
{"curie": "MONDO:0008775", "names": ["AMOBARBITAL, DEFICIENT N-HYDROXYLATION OF", "Amobarbital, Deficient N-Hydroxylation of", "Amobarbital, deficient N-hydroxylation of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Amobarbital, deficient N-hydroxylation of", "shortest_name_length": 41}
{"curie": "MONDO:0011055", "names": ["Dgs2", "DGS2", "10p deletion", "deletion 10p", "monosomy 10p", "10p monosomy", "Monosomy 10pter", "monosomy 10pter", "distal 10p deletion", "Distal 10p deletion", "distal monosomy 10p", "Distal monosomy 10p", "partial monosomy 10p", "Telomeric deletion 10p", "telomeric deletion 10p", "chromosome 10p deletion", "DiGeorge syndrome type 2", "distal monosomy type 10p", "DiGeorge Syndrome Type 2", "10p13-p14 Deletion Syndrome", "10p13-p14 Deletion syndrome", "Distal monosomy 10p (disorder)", "Digeorge Syndrome-Velocardiofacial Syndrome Complex 2", "DiGeorge syndrome/velocardiofacial syndrome complex 2", "DIGEORGE SYNDROME/VELOCARDIOFACIAL SYNDROME COMPLEX 2", "DiGeorge syndrome/velocardiofacial syndrome complex-2", "DiGeorge syndrome/velocardiofacial syndrome Complex type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal monosomy 10p", "shortest_name_length": 4}
{"curie": "UMLS:C0279643", "names": ["Colon Anaplastic Carcinoma", "Undifferentiated Colon Cancer", "Carcinoma simplex of the colon", "carcinoma simplex of the colon", "Carcinoma Simplex of the Colon.", "colon, carcinoma simplex of the", "Colon Undifferentiated Carcinoma", "Undifferentiated Colonic Carcinoma", "Undifferentiated Carcinoma of Colon", "Undifferentiated carcinoma of colon", "anaplastic adenocarcinoma of the colon", "colon, anaplastic adenocarcinoma of the", "Undifferentiated Carcinoma of the Colon", "undifferentiated adenocarcinoma of the colon", "colon, undifferentiated adenocarcinoma of the"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Undifferentiated Carcinoma of Colon", "shortest_name_length": 26}
{"curie": "UMLS:C5556455", "names": ["Uterine Corpus Epithelioid STUMP", "Uterine Corpus Epithelioid Smooth Muscle Tumor of Uncertain Malignant Potential"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Corpus Epithelioid Smooth Muscle Tumor of Uncertain Malignant Potential", "shortest_name_length": 32}
{"curie": "MONDO:0001382", "names": ["HEYD SYNDROME", "Heyd's syndrome", "Hepatorenal failure", "FAILURE HEPATORENAL", "UROHEPATIC SYNDROME", "Failure hepatorenal", "hepatorenal failure", "hepatorenal; failure", "Hepatorenal Syndrome", "failure; hepatorenal", "Hepatorenal syndrome", "HEPATORENAL SYNDROME", "Syndrome hepatorenal", "SYNDROME HEPATORENAL", "hepatorenal syndrome", "Syndrome, Hepatorenal", "syndrome; hepatorenal", "hepato-renal syndrome", "hepatorenal; syndrome", "HRF - Hepatorenal failure", "Hepatorenal syndrome (disorder)", "hepatorenal syndrome (diagnosis)", "RENAL FAILURE SECONDARY TO LIVER DISEASE HEPATORENAL SYNDROME", "RENAL FAILURE SECONDARY TO LIVER DISEASE <HEPATORENAL SYNDROME>"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatorenal syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0006801", "names": ["ileum tumor", "Ileal tumor", "ileal tumor", "Ileal Tumor", "Tumor of ileum", "tumor of ileum", "Tumor of Ileum", "ileum neoplasm", "ileal neoplasm", "Ileal Neoplasm", "Neoplasm, Ileal", "Ileal Neoplasms", "Tumour of ileum", "Neoplasms, Ileal", "Neoplasm of Ileum", "neoplasm of ileum", "Neoplasm of ileum", "Tumor of the Ileum", "tumor of the ileum", "neoplasm of the ileum", "benign ileal neoplasm", "Neoplasm of the Ileum", "ileum neoplasm (disease)", "Neoplasm of ileum (disorder)", "neoplasm of ileum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ileal neoplasm", "shortest_name_length": 11}
{"curie": "UMLS:C5670420", "names": ["Unresectable HER2-Positive Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable HER2-Positive Breast Carcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0007883", "names": ["PFITS", "Lazy Leukocyte Syndrome", "lazy leukocyte syndrome", "Lazy leucocyte syndrome", "LAZY LEUKOCYTE SYNDROME", "Lazy leukocyte syndrome", "Lazy leukocyte syndrome (disorder)", "Lazy leukocyte syndrome (diagnosis)", "defective cell chemotaxis lazy leukocyte syndrome", "periodic fever, immunodeficiency, and thrombocytopenia syndrome", "PERIODIC FEVER, IMMUNODEFICIENCY, AND THROMBOCYTOPENIA SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "periodic fever, immunodeficiency, and thrombocytopenia syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C1333029", "names": ["Choroid Spindle Cell Type B Melanoma", "Spindle Cell Type B Melanoma of Choroid", "Spindle Cell Type B Melanoma of the Choroid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Choroid Spindle Cell Type B Melanoma", "shortest_name_length": 36}
{"curie": "UMLS:C1333964", "names": ["DN", "Hepatic DN", "Liver Dysplastic Nodule", "Hepatic Dysplastic Nodule", "Dysplastic Nodule of Liver", "Dysplastic Nodule of the Liver"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liver Dysplastic Nodule", "shortest_name_length": 2}
{"curie": "MONDO:0035660", "names": ["GNAO1-related spectrum", "GNAO1-related developmental delay-seizures-movement disorder spectrum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "GNAO1-related developmental delay-seizures-movement disorder spectrum", "shortest_name_length": 22}
{"curie": "MONDO:0022729", "names": ["chondrodysplasia punctata with steroid sulfatase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chondrodysplasia punctata with steroid sulfatase deficiency", "shortest_name_length": 59}
{"curie": "MONDO:0003926", "names": ["pleura schwannoma", "pleural schwannoma", "Pleural Schwannoma", "schwannoma of pleura", "Schwannoma of Pleura", "pleural neurilemmoma", "Pleural Neurilemmoma", "neurilemmoma of pleura", "Neurilemmoma of Pleura", "Schwannoma of the Pleura", "schwannoma of the pleura", "Neurilemmoma of the Pleura", "neurilemmoma of the pleura"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurilemmoma of the pleura", "shortest_name_length": 17}
{"curie": "MONDO:0030996", "names": ["BDPLT24", "BLEEDING DISORDER, PLATELET-TYPE, 24", "bleeding disorder, platelet-type, 24", "bleeding disorder, platelet-type, 24, autosomal dominant", "GLANZMANN THROMBASTHENIA-LIKE WITH MACROTHROMBOCYTOPENIA 2", "Glanzmann Thrombasthenia-Like With Macrothrombocytopenia 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bleeding disorder, platelet-type, 24", "shortest_name_length": 7}
{"curie": "UMLS:C1336235", "names": ["stage IIIC endometrial cancer", "stage IIIC endometrial carcinoma", "stage IIIC uterine corpus cancer", "Stage IIIC Uterine Corpus Cancer", "Stage IIIC Uterine Corpus Cancer AJCC v7", "stage IIIC uterine corpus cancer AJCC v7", "Stage IIIC Uterine (including Endometrial) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Uterine Corpus Cancer AJCC v7", "shortest_name_length": 29}
{"curie": "MONDO:0012735", "names": ["TMBTS", "Temple-Baraitser syndrome", "Temple Baraitser syndrome", "TEMPLE-BARAITSER SYNDROME", "Temple-Baraitser Syndrome", "Temple Baraitser syndrome (disorder)", "Temple-Baraitser syndrome (diagnosis)", "severe mental retardation and absent nails of hallux and pollex", "mental retardation, severe, and absent nails of hallux and pollex", "Mental Retardation, Severe, And Absent Nails Of Hallux And Pollex", "MENTAL RETARDATION, SEVERE, AND ABSENT NAILS OF HALLUX AND POLLEX", "severe intellectual disability and absent nails of hallux and pollex", "intellectual disability, severe, and absent nails of hallux and pollex", "Severe intellectual disability, hypoplasia of thumb and hallux syndrome", "severe intellectual disability-aplasia/hypoplasia of thumb and hallux syndrome", "Severe intellectual disability-aplasia/hypoplasia of thumb and hallux syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Temple-Baraitser syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C1709735", "names": ["Prosthetic Valve Thrombosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prosthetic Valve Thrombosis", "shortest_name_length": 27}
{"curie": "UMLS:C0013142", "names": ["drown", "drowns", "drowned", "drowning", "DROWNING", "Drowning", "Drownings", "drownings", "Drowning NOS", "Drowning, NOS", "Drowning (event)", "drowning findings", "Fatal submersion-immersion", "Submersion-immersion, fatal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drowning", "shortest_name_length": 5}
{"curie": "UMLS:C1711386", "names": ["Nasal Cavity Keratinizing Squamous Cell Carcinoma", "Keratinizing Nasal Cavity Squamous Cell Carcinoma", "keratinizing squamous cell carcinoma of nasal cavity", "nasal cavity malignant carcinoma squamous cell keratinizing", "keratinizing squamous cell carcinoma of nasal cavity (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratinizing squamous cell carcinoma of nasal cavity", "shortest_name_length": 49}
{"curie": "MONDO:0018451", "names": ["X-linked dHMN", "X-linked distal spinal muscular atrophy", "X-linked distal hereditary motor neuropathy", "distal hereditary motor neuropathy, X-linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked distal hereditary motor neuropathy", "shortest_name_length": 13}
{"curie": "MONDO:0021134", "names": ["aFX", "acquired factor X deficiency", "Acquired Factor X Deficiency", "Acquired factor X deficiency", "Acquired factor 10 deficiency", "Acquired factor X deficiency disease", "Acquired Stuart factor deficiency disease", "Acquired factor X deficiency disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired factor X deficiency", "shortest_name_length": 3}
{"curie": "MONDO:0009058", "names": ["CYSTATHIONINURIA", "cystathioninuria", "Cystathioninuria", "Cystathioninuria, NOS", "CTH - Cystathioninuria", "Cystathionase deficiency", "CYSTATHIONASE DEFICIENCY", "Cystathionase Deficiency", "cystathionase deficiency", "cystathioninuria (disease)", "Deficiency of cystathionase", "Cystathioninuria (disorder)", "cystathioninuria (diagnosis)", "gamma-Cystathionase deficiency", "gamma-cystathionase deficiency", "Gamma-cystathionase deficiency", "homoserine deaminase deficiency", "High urine cystathionine levels", "Deficiency of homoserine deaminase", "Cystathione gamma-lyase deficiency", "Deficiency of cystine desulfhydrase", "Deficiency of cystine desulphydrase", "Deficiency of cysteine desulphydrase", "Deficiency of cysteine desulfhydrase", "Cystathionine gamma-lyase deficiency", "cystathione gamma-lyase deficiency syndrome", "Cystathione gamma-lyase deficiency syndrome", "Cystathionine gamma-lyase deficiency syndrome", "Cystathionine gamma-lyase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cystathioninuria", "shortest_name_length": 16}
{"curie": "UMLS:C1720798", "names": ["Radiation Recall Reaction", "radiation recall reaction", "Reaction, Radiation Recall", "Recall Reaction, Radiation", "Radiation Recall Reactions", "Recall Reactions, Radiation", "Radiation Recall Dermatitis", "Reactions, Radiation Recall", "Radiation recall dermatitis", "Radiation-Recall Dermatitis", "Dermatitis, Radiation Recall", "Radiation Recall Dermatitides", "Dermatitides, Radiation Recall", "radiation recall reaction (diagnosis)", "Radiation recall reaction (dermatologic)", "adverse drug effect of chemotherapeutics radiation recall reaction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radiation-Recall Dermatitis", "shortest_name_length": 25}
{"curie": "UMLS:C5557315", "names": ["DS Stage IIB Plasma Cell Myeloma", "Durie/Salmon Stage IIB Plasma Cell Myeloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DS Stage IIB Plasma Cell Myeloma", "shortest_name_length": 32}
{"curie": "MONDO:0009230", "names": ["multifocal fibrosclerosis", "Multifocal fibrosclerosis", "FIBROSCLEROSIS, MULTIFOCAL", "Fibrosclerosis, Multifocal", "fibrosclerosis, multifocal", "fibrosclerosis; multifocal", "multifocal; fibrosclerosis", "MEDIASTINAL FIBROSIS, FAMILIAL", "Mediastinal fibrosis, familial", "mediastinal fibrosis, familial", "RETROPERITONEAL FIBROSIS, FAMILIAL", "Retroperitoneal fibrosis, familial", "retroperitoneal fibrosis, familial", "Multifocal fibrosclerosis (disorder)", "multifocal fibrosclerosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibrosclerosis, multifocal", "shortest_name_length": 25}
{"curie": "MONDO:0003297", "names": ["gallbladder leiomyoma", "Gallbladder Leiomyoma", "gall bladder leiomyoma", "Leiomyoma of Gallbladder", "leiomyoma of gallbladder", "leiomyoma of gall bladder", "Leiomyoma of the Gallbladder", "leiomyoma of the gallbladder", "benign leiomyoma of gallbladder", "benign leiomyoma of gallbladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gallbladder leiomyoma", "shortest_name_length": 21}
{"curie": "MONDO:0020535", "names": ["house allergic alveolitis", "House allergic alveolitis", "House allergic alveolitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "house allergic alveolitis", "shortest_name_length": 25}
{"curie": "MONDO:0016584", "names": ["MAD", "mandibuloacral dysplasia", "mandibuloacral dysplasia with lipodystrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mandibuloacral dysplasia", "shortest_name_length": 3}
{"curie": "MONDO:0035678", "names": ["TS1", "LQT8 type 1", "Timothy syndrome type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Timothy syndrome type 1", "shortest_name_length": 3}
{"curie": "UMLS:C0543693", "names": ["Neutropenia neonatal", "Neonatal Neutropenia", "neonatal neutropenia", "Neonatal neutropenia", "neonatal; neutropenia", "neutropenia; neonatal", "Neonatal neutropenia (disorder)", "neonatal neutropenia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neonatal neutropenia (disorder)", "shortest_name_length": 20}
{"curie": "UMLS:C0278828", "names": ["stage IV bladder cancer", "Stage IV Bladder Cancer", "Stage IV Bladder Cancer AJCC v6", "Cancer of Bladder Stage IV AJCC v6", "Stage IV Bladder Carcinoma AJCC v6", "Stage IV Carcinoma of Bladder AJCC v6", "Cancer of the Bladder Stage IV AJCC v6", "Jewett-Marshall Stage D Bladder Cancer", "Jewett-Marshall Stage D Bladder Carcinoma", "Stage IV Carcinoma of the Bladder AJCC v6", "Stage IV Urinary Bladder Carcinoma AJCC v6", "Stage IV Carcinoma of Urinary Bladder AJCC v6", "Jewett-Marshall Stage D Urinary Bladder Cancer", "Stage IV Carcinoma of the Urinary Bladder AJCC v6", "Jewett-Marshall Stage D Urinary Bladder Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Bladder Cancer AJCC v6", "shortest_name_length": 23}
{"curie": "MONDO:0011361", "names": ["PCBC", "CAPB", "Capb", "Pcbc", "prostate cancer/brain cancer susceptibility", "PROSTATE CANCER/BRAIN CANCER SUSCEPTIBILITY", "prostate cancer/brain cancer susceptibility, somatic", "PROSTATE CANCER/BRAIN CANCER SUSCEPTIBILITY (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate cancer/brain cancer susceptibility", "shortest_name_length": 4}
{"curie": "MONDO:0007267", "names": ["CMH3", "hypertrophic cardiomyopathy 3", "cardiomyopathy, hypertrophic, 3", "TPM1 hypertrophic cardiomyopathy", "hypertrophic cardiomyopathy type 3", "cardiomyopathy familial hypertrophic 3", "Cardiomyopathy, Familial Hypertrophic, 3", "CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 3", "cardiomyopathy, familial hypertrophic, 3", "Familial Hypertrophic Cardiomyopathy Type 3", "cardiomyopathy, familial hypertrophic, type 3", "hypertrophic cardiomyopathy caused by mutation in TPM1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophic cardiomyopathy 3", "shortest_name_length": 4}
{"curie": "UMLS:C2985399", "names": ["hepatic arterial occlusion", "Hepatic Arterial Occlusion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatic Arterial Occlusion", "shortest_name_length": 26}
{"curie": "UMLS:C1336706", "names": ["Testicular Dermoid Cyst"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular Dermoid Cyst", "shortest_name_length": 23}
{"curie": "UMLS:C4289768", "names": ["Colon Adenoma with Severe Dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colon Adenoma with Severe Dysplasia", "shortest_name_length": 35}
{"curie": "MONDO:0016624", "names": ["inherited deficiency anemia", "constitutional rare deficiency anemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited deficiency anemia", "shortest_name_length": 27}
{"curie": "UMLS:C3274509", "names": ["Recto-Vesico-Vaginal Fistula", "Rectal-Vesico-Vaginal Fistula"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recto-Vesico-Vaginal Fistula", "shortest_name_length": 28}
{"curie": "MONDO:0019678", "names": ["brachydactyly type A5", "Brachydactyly type A5", "Type A5 brachydactyly", "Brachydactyly type A5 (disorder)", "brachydactyly type A5 nail dysplasia", "Brachydactyly type A5 nail dysplasia", "Brachydactyly, Type A5, With Nail Dysplasia", "Absent middle phalanges of digits 2-5 with nail dysplasia", "absent middle phalanges of digits 2-5 with nail dysplasia", "brachydactyly with absence of middle phalanges and hypoplastic nails"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly type A5", "shortest_name_length": 21}
{"curie": "UMLS:C2981270", "names": ["Stage IVA Differentiated Thyroid Gland Cancer", "Stage IVA Differentiated Thyroid Gland Carcinoma", "Stage IVA Differentiated Thyroid Gland Carcinoma AJCC v7", "Stage IVA Thyroid Gland Papillary or Follicular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Differentiated Thyroid Gland Carcinoma AJCC v7", "shortest_name_length": 45}
{"curie": "UMLS:C3897720", "names": ["Renal Allograft Thrombosis", "Kidney Allograft Thrombosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal Allograft Thrombosis", "shortest_name_length": 26}
{"curie": "MONDO:0024301", "names": ["mineral metabolism disease", "acquired mineral metabolism disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired mineral metabolism disease", "shortest_name_length": 26}
{"curie": "MONDO:0017177", "names": ["HHML", "hemihyperplasia-multiple lipomatosis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemihyperplasia-multiple lipomatosis syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0009026", "names": ["CSTLO", "CMEMS", "FCS SYNDROME", "FCS syndrome", "FCS Syndrome", "Syndrome, FCS", "FCS Syndromes", "Syndromes, FCS", "Costello Syndrome", "costello syndrome", "COSTELLO SYNDROME", "Costello syndrome", "Syndrome, Costello", "Costello syndrome (disorder)", "faciocutaneoskeletal syndrome", "FACIOCUTANEOSKELETAL SYNDROME", "Faciocutaneoskeletal Syndrome", "costello syndrome (diagnosis)", "Faciocutaneoskeletal syndrome", "Faciocutaneoskeletal Syndromes", "Syndrome, Faciocutaneoskeletal", "Syndromes, Faciocutaneoskeletal", "faciocutaneoskeletal (FCS) syndrome", "congenital myopathy with excess of muscle spindles", "myopathy, congenital, with excess of muscle spindles", "MYOPATHY, CONGENITAL, WITH EXCESS OF MUSCLE SPINDLES", "Myopathy, Congenital, With Excess Of Muscle Spindles"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Costello syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0272426", "names": ["mouth injury", "Mouth injury", "injury mouth", "mouth; injury", "injury; mouth", "Injured mouth", "injuries mouth", "injury of mouth", "Injury of mouth", "Injury of oral cavity", "injuries of oral cavity", "Injury of mouth (disorder)", "injury of mouth (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of mouth", "shortest_name_length": 12}
{"curie": "MONDO:0021310", "names": ["Neck Cancer", "neck cancer", "cancer neck", "NECK CANCER", "cancers neck", "Cancer, Neck", "Neck Cancers", "Neck--Cancer", "Cancers, Neck", "cancer neck of", "cancer of neck", "of neck cancer", "Cancer of Neck", "cancer of the neck", "Cancer of the Neck", "Malignant Neck Tumor", "malignant neck tumor", "malignant neck tumors", "Malignant Neck Neoplasm", "Malignant Tumor of Neck", "Malignant tumor of neck", "malignant neck neoplasm", "malignant tumor of neck", "Malignant tumour of neck", "Malignant Neoplasm of Neck", "malignant neoplasm of neck", "Malignant Tumor of the Neck", "malignant tumor of the neck", "malignant neoplasm of the neck", "Malignant Neoplasm of the Neck", "Malignant neoplasm of neck, NOS", "Malignant tumor of neck (disorder)", "malignant neoplasm of neck (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant tumor of neck", "shortest_name_length": 11}
{"curie": "MONDO:0019242", "names": ["inborn branched chain aminoaciduria", "branched-chain; amino-acid disorder", "branched chain amino acid metabolism disorder", "Branched chain amino acid metabolism disorder", "amino-acid; metabolic disorder, branched-chain", "metabolic disorder; amino-acid, branched-chain", "branched-chain amino-acid metabolism; disorder", "disorder; branched-chain amino-acid metabolism", "disorder of branched-chain amino acid metabolism", "disorder of branched chain amino acid metabolism", "Disorder of branched-chain amino acid metabolism", "Disorder of branched chain amino acid metabolism", "branched-chain amino-acid metabolism disturbances", "Disturbances of branched-chain amino-acid metabolism", "inborn disorder of branched-chain amino acid metabolism", "inborn branched-chain amino acid metabolic process disorder", "Disorder of branched-chain amino acid metabolism (disorder)", "inborn error of branched-chain amino acid metabolic process", "Disturbances of metabolism of leucine, isoleucine and valine", "Disorder of branched-chain amino-acid metabolism, unspecified", "branched-chain amino-acid metabolism disturbances (diagnosis)", "rare inborn error of branched-chain amino acid metabolic process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of branched-chain amino acid metabolism", "shortest_name_length": 35}
{"curie": "MONDO:0009100", "names": ["IDDM", "IDDM1", "juvenile-onset diabetes", "type 1 diabetes mellitus", "diabetes mellitus, type 1", "type 1 diabetes mellitus 1", "diabetes, type 1, susceptibility to", "diabetes mellitus, insulin-dependent", "insulin-dependent diabetes mellitus 1", "diabetes mellitus, insulin-dependent-1", "diabetes mellitus, insulin-dependent, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "type 1 diabetes mellitus 1", "shortest_name_length": 4}
{"curie": "MONDO:0013717", "names": ["ATD5", "SRTD5", "WDR19 Jeune syndrome", "asphyxiating thoracic dystrophy 5", "ASPHYXIATING THORACIC DYSTROPHY 5", "asphyxiating thoracic dystrophy type 5", "Jeune syndrome caused by mutation in WDR19", "short-rib thoracic dysplasia 5 with or without polydactyly", "SHORT-RIB THORACIC DYSPLASIA 5 WITH OR WITHOUT POLYDACTYLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "asphyxiating thoracic dystrophy 5", "shortest_name_length": 4}
{"curie": "MONDO:0011171", "names": ["Otudp syndrome", "OTUDP SYNDROME", "OTUDP syndrome", "ODONTOTRICHOUNGUAL-digital-palmar syndrome", "Odontotrichoungual-Digital-Palmar Syndrome", "Odontotrichoungual-digital-palmar syndrome", "ODONTOTRICHOUNGUAL-DIGITAL-PALMAR SYNDROME", "odonto-tricho-ungual-digito-palmar syndrome", "Odonto-tricho-ungual-digito-palmar syndrome", "Odonto-tricho-ungual-digito-palmar syndrome (disorder)", "Odonto-tricho-ungual-digito-palmar syndrome Mendoza-Valiente type", "Odonto-tricho-ungual-digito-palmar syndrome, Mendoza-Valiente type", "odonto-tricho-ungual-digito-palmar syndrome, Mendoza-Valiente type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "odonto-tricho-ungual-digito-palmar syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C3272525", "names": ["MEITL", "Type II EATL", "Monomorphic CD56+ Intestinal T-Cell Lymphoma", "Monomorphic epitheliotropic intestinal T-cell lymphoma", "Monomorphic Epitheliotropic Intestinal T-Cell Lymphoma", "Monomorphic epitheliotropic intestinal T-cell lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Monomorphic epitheliotropic intestinal T-cell lymphoma", "shortest_name_length": 5}
{"curie": "MONDO:0036696", "names": ["spleen tumor", "tumor of spleen", "spleen neoplasm", "Splenic Neoplasm", "splenic neoplasm", "neoplasm of spleen"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spleen neoplasm", "shortest_name_length": 12}
{"curie": "UMLS:C0475728", "names": ["Subgaleal hematoma", "Subgaleal haematoma", "Subgaleal hemorrhage", "Subgaleal Hemorrhage", "Subgaleal haemorrhage", "Subaponeurotic hematoma", "Subaponeurotic haematoma", "Subaponeurotic hemorrhage", "Subaponeurotic haemorrhage", "Epicranial subaponeurotic hematoma", "Epicranial subaponeurotic haematoma", "Epicranial subaponeurotic hemorrhage", "Epicranial subaponeurotic haemorrhage", "Epicranial subaponeurotic hematoma (disorder)", "Epicranial subaponeurotic hemorrhage (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subgaleal hemorrhage", "shortest_name_length": 18}
{"curie": "MONDO:0020553", "names": ["secondary pulmonary hemosiderosis", "Secondary pulmonary hemosiderosis", "Secondary pulmonary haemosiderosis", "Secondary pulmonary hemosiderosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary pulmonary hemosiderosis", "shortest_name_length": 33}
{"curie": "UMLS:C4526720", "names": ["Stage IIB", "Stage IIB Lung Cancer", "Stage IIB Lung Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Lung Cancer AJCC v8", "shortest_name_length": 9}
{"curie": "MONDO:0009844", "names": ["Pellagra-Like Syndrome", "pellagra-like syndrome", "PELLAGRA-LIKE SYNDROME", "Pellagra like syndrome", "pellagra like syndrome", "Pellagra-like rash with neurologic manifestations", "pellagra-like rash with neurologic manifestations", "pellagra-like skin rash-neurological manifestations syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pellagra-like syndrome", "shortest_name_length": 22}
{"curie": "MONDO:0700043", "names": ["syndrome caused by partial chromosomal duplication of the short arm of chromosome 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndrome caused by partial chromosomal duplication of the short arm of chromosome 9", "shortest_name_length": 83}
{"curie": "MONDO:0021339", "names": ["Hard Palate Carcinoma", "hard palate carcinoma", "carcinoma of hard palate", "Carcinoma of hard palate", "Carcinoma of Hard Palate", "carcinoma of the hard palate", "Carcinoma of the Hard Palate", "Carcinoma of hard palate (disorder)", "Carcinoma of hard palate (diagnosis)", "hard palate neoplasm malignant carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma of hard palate", "shortest_name_length": 21}
{"curie": "MONDO:0014794", "names": ["MGORS6", "Meier-GORLIN syndrome 6", "Meier-Gorlin syndrome 6", "MEIER-GORLIN SYNDROME 6", "GMNN Meier-Gorlin syndrome", "Meier-Gorlin syndrome type 6", "Meier-Gorlin syndrome caused by mutation in GMNN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meier-Gorlin syndrome 6", "shortest_name_length": 6}
{"curie": "UMLS:C0016722", "names": ["Frigidity", "frigidity", "Frigidity, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Frigidity", "shortest_name_length": 9}
{"curie": "MONDO:0008767", "names": ["JNCL", "CLN3", "CLN3 disease", "Juvenile NCL", "batten disease", "Batten Disease", "Batten disease", "BATTEN DISEASE", "battens disease", "Disease, Batten", "Spielmeyer-Vogt", "Vogt-Spielmeyer", "batten's disease", "Batten's disease", "Batten's syndrome", "batten's syndrome", "Batten-Mayou Disease", "Batten-Mayou disease", "Batten Mayou Disease", "Batten-Mayou syndrome", "CLN3 disease, juvenile", "Spielmeyer-Vogt disease", "Vogt-Spielmeyer disease", "Spielmeyer Vogt Disease", "Vogt-Spielmeyer Disease", "spielmeyer-vogt disease", "VOGT-SPIELMEYER DISEASE", "Juvenile Batten Disease", "Vogt Spielmeyer disease", "Vogt Spielmeyer Disease", "Spielmeyer-Vogt Disease", "Juvenile Batten Diseases", "Disease, Juvenile Batten", "Disease, Vogt-Spielmeyer", "Spielmeyer Disease, Vogt", "Disease, Spielmeyer-Vogt", "Batten Disease, Juvenile", "Disease, Vogt Spielmeyer", "Batten Diseases, Juvenile", "Spielmeyer Sjogren Disease", "Spielmeyer-Sjogren disease", "Spielmeyer-Sjogren Disease", "Spielmeyer Sjogren disease", "SPIELMEYER-SJOGREN DISEASE", "Disease, Spielmeyer-Sjogren", "Batten-Spielmeyer-Vogt disease", "Batten-Spielmeyer-Vogt Disease", "Batten Spielmeyer Vogt Disease", "Amaurotic idiocy juvenile type", "Amaurotic idiocy, juvenile type", "neuronal ceroid lipofuscinosis 3", "Neuronal lipofuscinosis, juvenile", "ceroid lipofuscinosis, neuronal, 3", "CEROID LIPOFUSCINOSIS, NEURONAL, 3", "Ceroid Lipofuscinosis, Neuronal, 3", "CLN3 neuronal ceroid lipofuscinosis", "neuronal ceroid lipofuscinosis CLN3", "Juvenile Cerebroretinal Degeneration", "Cerebral lipidosis myoclonic variant", "Cerebroretinal Degeneration, Juvenile", "neuronal ceroid lipofuscinosis type 3", "Cerebral lipidosis, myoclonic variant", "Neuronal Ceroid Lipofuscinosis Type 3", "Juvenile Cerebroretinal Degenerations", "Neuronal lipofuscinosis, late juvenile", "Cerebroretinal Degenerations, Juvenile", "ceroid lipofuscinosis, neuronal, type 3", "Juvenile neuronal ceroid lipofuscinosis", "juvenile neuronal ceroid lipofuscinosis", "Juvenile Neuronal Ceroid Lipofuscinosis", "neuronal ceroid lipofuscinosis, juvenile", "Neuronal Ceroid Lipofuscinosis, Juvenile", "NEURONAL CEROID LIPOFUSCINOSIS, JUVENILE", "Ceroid Lipofuscinosis, Neuronal 3, Juvenile", "CLN3-Related Neuronal Ceroid-Lipofuscinoses", "CLN3 Related Neuronal Ceroid Lipofuscinosis", "CLN3-Related Neuronal Ceroid-Lipofuscinosis", "Neuronal Ceroid-Lipofuscinoses, CLN3-Related", "Ceroid-Lipofuscinosis, CLN3-Related Neuronal", "Neuronal Ceroid Lipofuscinosis Juvenile Type", "Neuronal Ceroid-Lipofuscinosis, CLN3-Related", "neuronal ceroid lipofuscinosis CLN3 (diagnosis)", "Juvenile neuronal ceroid lipofuscinosis (disorder)", "Spielmeyer-Vogt type neuronal ceroid lipofuscinosis", "neuronal ceroid lipofuscinosis CLN3 (Batten disease)", "neuronal ceroid lipofuscinosis caused by mutation in CLN3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuronal ceroid lipofuscinosis 3", "shortest_name_length": 4}
{"curie": "UMLS:C1332495", "names": ["Esophageal Schwannoma", "Benign Esophagus Schwannoma", "Benign Esophageal Schwannoma", "Benign Esophagus Neurilemmoma", "Benign Schwannoma of Esophagus", "Benign Esophageal Neurilemmoma", "Benign Neurilemmoma of Esophagus", "Benign Schwannoma of the Esophagus", "Benign Neurilemmoma of the Esophagus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Schwannoma", "shortest_name_length": 21}
{"curie": "MONDO:0009743", "names": ["neurologic disease, infantile multisystem, with osseous fragility", "NEUROLOGIC DISEASE, INFANTILE MULTISYSTEM, WITH OSSEOUS FRAGILITY", "Neurologic Disease, Infantile Multisystem, with Osseous Fragility"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurologic disease, infantile multisystem, with osseous fragility", "shortest_name_length": 65}
{"curie": "MONDO:0009295", "names": ["GSD7", "Tauri", "GSD 7", "GSDVII", "gsd vii", "GSD VII", "GSD type 7", "GSD type VII", "Tarui disease", "Tauri disease", "Tarui Disease", "TARUI DISEASE", "tauri disease", "disease tarui", "tarui disease", "Disease, Tarui", "taruis disease", "Glycogenosis 7", "Taruis Disease", "Tarui's disease", "PFKM DEFICIENCY", "Pfkm deficiency", "Pfkm Deficiency", "PFKM Deficiency", "Tarui's Disease", "tarui's disease", "diseases tarui's", "Deficiency, Pfkm", "Disease, Tarui's", "Pfkm Deficiencies", "Deficiencies, Pfkm", "glycogenosis type 7", "Glycogenosis type 7", "GLYCOGENOSIS TYPE VII", "Glycogenosis type VII", "glycogenosis type VII", "glycogen storage disease 7", "Glycogen storage disease 7", "Tarui's disease (diagnosis)", "Glycogen Storage Disease VII", "glycogen storage disease VII", "phosphofructokinase myopathy", "GLYCOGEN STORAGE DISEASE VII", "PFKM glycogen storage disease", "phosphofructokinase deficiency", "Phosphofructokinase Deficiency", "PHOSPHOFRUCTOKINASE DEFICIENCY", "Glycogen storage disease type 7", "glycogen storage disease type 7", "Glycogen storage disease, type 7", "Glycogen storage disease type VII", "GLYCOGEN STORAGE DISEASE TYPE VII", "glycogen storage disease type VII", "Glycogen Storage Disease Type VII", "Glycogen storage disease, type VII", "glycogen storage disease, type VII", "MUSCLE PHOSPHOFRUCTOKINASE DEFICIENCY", "muscle phosphofructokinase deficiency", "Muscle phosphofructokinase deficiency", "Muscle Phosphofructokinase Deficiency", "Deficiency, Muscle Phosphofructokinase", "Phosphofructokinase Deficiency, Muscle", "Muscle Phosphofructokinase Deficiencies", "Deficiencies, Muscle Phosphofructokinase", "Phosphofructokinase Deficiencies, Muscle", "PFK - Muscle phosphofructokinase deficiency", "glycogen storage disease type VII (diagnosis)", "Glycogen storage disease, type VII (disorder)", "GSD due to muscle phosphofructokinase deficiency", "glycogen storage disease caused by mutation in PFKM", "glycogenosis due to muscle phosphofructokinase deficiency", "Glycogenosis due to muscle phosphofructokinase deficiency", "glycogen storage disease due to muscle phosphofructokinase deficiency", "Glycogen storage disease due to muscle phosphofructokinase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease VII", "shortest_name_length": 4}
{"curie": "MONDO:0001881", "names": ["tss", "TSS", "Toxic Shock", "toxic shock", "SHOCK SEPTIC", "toxic; shock", "Shock, Toxic", "septic shock", "Shock septic", "SEPTIC SHOCK", "Septic shock", "Septic Shock", "Shock, Septic", "Bacterial TSS", "shock; septic", "septic; shock", "bacterial TSS", "septicemic shock", "Septicemic shock", "Septicaemic shock", "toxic shock syndrome", "Toxic shock syndrome", "Syndrome toxic shock", "Toxic Shock Syndrome", "TOXIC-SHOCK SYNDROME", "SYNDROME TOXIC SHOCK", "toxic-shock syndrome", "TOXIC SHOCK SYNDROME", "shock syndrome; toxic", "toxic; shock syndrome", "Shock Syndrome, Toxic", "Systemic Septic Shock", "Toxic Shock Syndromes", "syndrome; toxic shock", "shock; toxic (syndrome)", "Septic shock (disorder)", "Toxic shock syndrome NOS", "septic shock (diagnosis)", "TSS, toxic shock syndrome", "Gram-positive septic shock", "TSS - Toxic shock syndrome", "toxic shock syndrome (TSS)", "shock syndrome (TSS), toxic", "toxic shock syndrome, (TSS)", "syndrome (TSS), toxic shock", "Gramme-positive septic shock", "Sepsis-associated hypotension", "Bacterial toxic-shock syndrome", "bacterial toxic-shock syndrome", "Toxic shock syndrome (disorder)", "toxic shock syndrome (diagnosis)", "staphylococcal toxic shock syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "toxic shock syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0005796", "names": ["HIV enteropathy", "HIV Enteropathy", "AIDS enteropathy", "AIDS Enteropathy", "Enteropathy, HIV", "Enteropathy, AIDS", "HIV Enteropathies", "Enteropathies, HIV", "AIDS Enteropathies", "Enteropathies, AIDS", "HIV Associated Enteropathy", "HIV-Associated Enteropathy", "Idiopathic AIDS Enteropathy", "HIV enteropathy (diagnosis)", "Enteropathy, HIV Associated", "Enteropathy, HIV-Associated", "AIDS Associated Enteropathy", "AIDS-Associated Enteropathy", "HIV-Associated Enteropathies", "AIDS Enteropathy, Idiopathic", "Enteropathy, AIDS Associated", "Enteropathy, Idiopathic AIDS", "Enteropathy, AIDS-Associated", "Idiopathic AIDS Enteropathies", "Enteropathies, HIV-Associated", "AIDS-Associated Enteropathies", "Enteropathies, Idiopathic AIDS", "Enteropathies, AIDS-Associated", "AIDS Enteropathies, Idiopathic", "infectious diarrhea of HIV patient", "Human immunodeficiency virus diarrhea", "Human immunodeficiency virus diarrhoea", "Human immunodeficiency virus enteropathy", "HIV - Human immunodeficiency virus diarrhea", "HIV - Human immunodeficiency virus diarrhoea", "HIV - Human immunodeficiency virus enteropathy", "infectious diarrhea of HIV patient (diagnosis)", "Human immunodeficiency virus enteropathy (disorder)", "Human immunodeficiency virus non-pathogenic diarrhea", "Human immunodeficiency virus non-pathogenic diarrhoea"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HIV enteropathy", "shortest_name_length": 15}
{"curie": "MONDO:0012979", "names": ["CILD12", "primary ciliary dyskinesia 12", "ciliary dyskinesia, primary, 12", "CILIARY DYSKINESIA, PRIMARY, 12", "Ciliary Dyskinesia, Primary, 12", "RSPH9 primary ciliary dyskinesia", "primary ciliary dyskinesia type 12", "ciliary dyskinesia, primary, type 12", "primary ciliary dyskinesia 12 without situs inversus", "primary ciliary dyskinesia caused by mutation in RSPH9", "ciliary dyskinesia, primary, 12, without situs inversus", "CILIARY DYSKINESIA, PRIMARY, 12, WITHOUT SITUS INVERSUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary ciliary dyskinesia 12", "shortest_name_length": 6}
{"curie": "MONDO:0000628", "names": ["central nervous system benign neoplasm", "central nervous system organ benign neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system organ benign neoplasm", "shortest_name_length": 38}
{"curie": "UMLS:C2348370", "names": ["Early Unfavorable Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Early Unfavorable Hodgkin Lymphoma", "shortest_name_length": 34}
{"curie": "UMLS:C0334558", "names": ["Odontogenic sarcoma", "Odontogenic Sarcoma", "ODONTOMA, MALIGNANT", "odontogenic; sarcoma", "sarcoma; odontogenic", "Odontogenic carcinoma", "odontogenic; carcinoma", "Intraosseous carcinoma", "carcinoma; odontogenic", "intraosseous; carcinoma", "carcinoma; intraosseous", "Malignant odontogenic tumor", "Malignant Odontogenic Tumor", "Malignant odontogenic tumour", "Odontogenic tumor, malignant", "Odontogenic tumour, malignant", "tumor; odontogenic, malignant", "odontogenic; tumor, malignant", "Malignant Odontogenic Neoplasm", "Primary intraosseous carcinoma", "Primary intra-osseous carcinoma", "Carcinoma arising in an odontogenic cyst", "Odontogenic tumor, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant odontogenic tumor", "shortest_name_length": 19}
{"curie": "UMLS:C5555529", "names": ["Melanoma Metastatic in the Brain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Melanoma Metastatic in the Brain", "shortest_name_length": 32}
{"curie": "UMLS:C1706708", "names": ["Acute Myelomonocytic Leukemia without Abnormal Eosinophils"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Myelomonocytic Leukemia without Abnormal Eosinophils", "shortest_name_length": 58}
{"curie": "UMLS:C4744459", "names": ["Locally Advanced Digestive System Neuroendocrine Carcinoma", "Locally Advanced Gastrointestinal System Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Digestive System Neuroendocrine Carcinoma", "shortest_name_length": 58}
{"curie": "MONDO:0018528", "names": ["congenital myopathy with myasthenic-like onset", "Congenital myopathy with myasthenic-like onset", "Congenital myopathy with myasthenic-like onset (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myopathy with myasthenic-like onset", "shortest_name_length": 46}
{"curie": "UMLS:C5421291", "names": ["Sinonasal Leiomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Leiomyosarcoma", "shortest_name_length": 24}
{"curie": "UMLS:C2981925", "names": ["Stage I Skin Melanoma AJCC v7", "Stage I Cutaneous (Skin) Melanoma", "Stage I Cutaneous Melanoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Cutaneous Melanoma AJCC v7", "shortest_name_length": 29}
{"curie": "UMLS:C1336869", "names": ["Unresectable Malignant Tumor", "Unresectable Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Malignant Neoplasm", "shortest_name_length": 28}
{"curie": "MONDO:0005613", "names": ["MNAC", "Mesonephroma", "mesonephroma", "MESONEPHROMAS", "Mesonephromas", "Mesonephroma, NOS", "Mesonephric Carcinoma", "Malignant Mesonephroma", "malignant mesonephroma", "Malignant mesonephroma", "Mesonephroma, malignant", "Wolffian duct carcinoma", "Mesometanephric carcinoma", "Mesonephric adenocarcinoma", "Mesonephric Adenocarcinoma", "mesonephric adenocarcinoma", "malignant mesonephroma (diagnosis)", "Mesonephroma, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mesonephric adenocarcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0018062", "names": ["Trueb Burg Bottani syndrome", "Trueb-Burg-Bottani syndrome", "Ectodermal dysplasia with corkscrew hairs", "ectodermal dysplasia with corkscrew hairs", "Tricho-odonto-onychodysplasia with syndactyly", "autosomal dominant trichoodontoonychodysplasia-syndactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant trichoodontoonychodysplasia-syndactyly", "shortest_name_length": 27}
{"curie": "MONDO:0001144", "names": ["Partial Third-Nerve Palsy", "Partial Third Nerve Palsy", "partial third-nerve palsy", "partial third nerve palsy", "Partial third nerve palsy", "Palsy, Partial Third-Nerve", "Third-Nerve Palsy, Partial", "Third nerve palsy - partial", "Partial Third-Nerve Palsies", "Third-Nerve Palsies, Partial", "Partial oculomotor nerve palsy", "partial third cranial nerve palsy", "Third nerve palsy with pupil sparing", "third nerve palsy with pupil sparing", "Partial third cranial nerve paralysis", "partial third nerve palsy (diagnosis)", "third or oculomotor nerve palsy, partial", "Third or oculomotor nerve palsy, partial", "Partial oculomotor nerve palsy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial third-nerve palsy", "shortest_name_length": 25}
{"curie": "MONDO:0700126", "names": ["trisomy 21"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trisomy 21", "shortest_name_length": 10}
{"curie": "MONDO:0004691", "names": ["ADPKD", "adpkd", "Congenital biliary ectasias", "congenital biliary ectasias", "Polycystic kidney, adult type", "polycystic; kidney, adult type", "adult disease kidney polycystic", "Adult Polycystic Kidney Disease", "adult polycystic kidney disease", "Polycystic kidneys - adult type", "POLYCYSTIC KIDNEY DISEASE, ADULT", "Polycystic Kidney Disease, Adult", "cyst; kidney, multiple, adult type", "Autosomal Dominant Polycystic Kidney", "Polycystic Kidney, Autosomal Dominant", "Polycystic kidney, autosomal dominant", "Polycystic kidney disease, adult type", "Kidney, Polycystic, Autosomal Dominant", "POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1", "Autosomal Dominant Polycystic Kidney Disease", "autosomal dominant polycystic kidney disease", "Autosomal dominant polycystic kidney disease", "polycystic; degeneration, kidney, adult type", "Polycystic Kidney Disease, Autosomal Dominant", "polycystic kidney disease, autosomal dominant", "Autosomal dominant adult polycystic kidney disease", "ADPKD - Autosomal dominant polycystic kidney disease", "ADPKD - autosomal dominant polycystic kidney disease", "Autosomal dominant polycystic kidney disease (disorder)", "autosomal dominant polycystic kidney disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant polycystic kidney disease", "shortest_name_length": 5}
{"curie": "MONDO:0003017", "names": ["malignant peritoneal solitary fibrous tumor", "peritoneal solitary fibrous tumor, malignant", "malignant peritoneal solitary fibrous tumour", "pleural and peritoneal solitary fibrous tumor", "Pleural and peritoneal Solitary fibrous tumor", "Pleural and peritoneal Solitary fibrous tumour"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant peritoneal solitary fibrous tumor", "shortest_name_length": 43}
{"curie": "UMLS:C1827431", "names": ["Head and Neck Sarcoma", "Sarcoma of head and neck", "Sarcoma of head and neck (disorder)", "malignant neoplasm sarcoma of head and neck", "malignant neoplasm sarcoma of head and neck (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sarcoma of head and neck", "shortest_name_length": 21}
{"curie": "MONDO:0010267", "names": ["EMWX", "Episodic Muscle Weakness, X-Linked", "EPISODIC MUSCLE WEAKNESS, X-LINKED", "episodic muscle weakness, X-linked"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "episodic muscle weakness, X-linked", "shortest_name_length": 4}
{"curie": "UMLS:C5206803", "names": ["Metastatic Papillary Renal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Papillary Renal Cell Carcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0018903", "names": ["Sarcocystoses", "Sacocystiosis", "sarcocystosis", "Sarcocystosis", "Sarcocystiosis", "sarcosporidiosis", "Sarcosporidiasis", "Sarcosporidioses", "Sarcosporidiosis", "Sarcocystis infection", "infection; sarcocystis", "sarcocystis; infection", "Sarcocystis infections", "Sarcosporidiosis (disorder)", "sarcosporidiosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sarcocystosis", "shortest_name_length": 13}
{"curie": "UMLS:C3899645", "names": ["Pleomorphic Xanthoastrocytoma", "childhood pleomorphic xanthoastrocytoma", "Childhood Pleomorphic Xanthoastrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Pleomorphic Xanthoastrocytoma", "shortest_name_length": 29}
{"curie": "MONDO:0014921", "names": ["DEE43", "EIEE43", "early infantile epileptic encephalopathy 43", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43", "epileptic encephalopathy, early infantile, 43", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 43", "developmental and epileptic encephalopathy 43", "developmental and epileptic encephalopathy, 43", "GABRB3 early infantile epileptic encephalopathy", "epileptic encephalopathy, early infantile, type 43", "epileptic encephalopathy, early infantile, 43; EIEE43", "early infantile epileptic encephalopathy caused by mutation in GABRB3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 43", "shortest_name_length": 5}
{"curie": "MONDO:0013645", "names": ["SCAR11", "autosomal recessive spinocerebellar ataxia 11", "spinocerebellar ataxia, autosomal recessive 11", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 11", "Autosomal recessive spinocerebellar ataxia type 11", "autosomal recessive spinocerebellar ataxia type 11", "spinocerebellar ataxia, autosomal recessive type 11", "SYT14 autosomal recessive syndromic cerebellar ataxia", "Autosomal recessive cerebellar ataxia-psychomotor delay syndrome", "Autosomal recessive cerebellar ataxia, psychomotor delay syndrome", "autosomal recessive cerebellar ataxia-psychomotor retardation syndrome", "autosomal recessive syndromic cerebellar ataxia caused by mutation in SYT14", "Autosomal recessive cerebellar ataxia, psychomotor delay syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive spinocerebellar ataxia 11", "shortest_name_length": 6}
{"curie": "MONDO:0003916", "names": ["Overfed", "overnutrition", "Overnutrition", "Hypernutrition", "Disorder of hyperalimentation", "Disorder of hyperalimentation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "overnutrition", "shortest_name_length": 7}
{"curie": "UMLS:C0011389", "names": ["plaque", "Plaque", "tooth plaque", "Tooth plaque", "Dental plaque", "Dental Plaque", "dental plaque", "dental plaques", "teeth; plaques", "Plaque, Dental", "plaques; teeth", "Dental plaque on teeth", "Dental plaque on tooth", "Dental plaque formation", "Dental biofilm on tooth", "dental plaque (diagnosis)", "Observation of tooth plaque", "Dental plaque on teeth (disorder)", "Dental plaque on tooth (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dental Plaque", "shortest_name_length": 6}
{"curie": "MONDO:0100218", "names": ["AMC5", "arthrogryposis multiplex congenita 5", "ARTHROGRYPOSIS MULTIPLEX CONGENITA 5", "arthrogryposis multiplex congenita-5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis multiplex congenita 5", "shortest_name_length": 4}
{"curie": "UMLS:C2981178", "names": ["Stage III Penile Cancer", "Stage III Penis Cancer AJCC v6", "Stage III Penile Cancer AJCC v6", "Penile Cancer Stage III AJCC v6", "Stage III Penis Carcinoma AJCC v6", "Penile Carcinoma Stage III AJCC v6", "Stage III Penile Carcinoma AJCC v6", "Stage III Carcinoma of Penis AJCC v6", "Stage III Carcinoma of the Penis AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Penile Cancer AJCC v6", "shortest_name_length": 23}
{"curie": "UMLS:C0278786", "names": ["Recurrent Brain Neoplasm", "adult CNS tumor, recurrent", "Relapsed Adult Brain Tumor", "recurrent CNS tumor, adult", "recurrent adult brain tumor", "Recurrent Adult Brain Tumor", "recurrent brain tumor, adult", "adult brain tumor, recurrent", "Relapsed Adult Brain Neoplasm", "Relapsed Tumor of Adult Brain", "brain tumor, recurrent, adult", "Recurrent Tumor of Adult Brain", "Recurrent Adult Brain Neoplasm", "Relapsed Neoplasm of Adult Brain", "Relapsed Tumor of the Adult Brain", "CNS tumor, adult brain, recurrent", "Recurrent Neoplasm of Adult Brain", "Recurrent Tumor of the Adult Brain", "Relapsed Neoplasm of the Adult Brain", "Recurrent Neoplasm of the Adult Brain", "central nervous system tumor, recurrent, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Adult Brain Neoplasm", "shortest_name_length": 24}
{"curie": "MONDO:0024876", "names": ["tendon sheath disease", "Tendon sheath disorder", "tendon sheath disorder", "disease of tendon sheath", "disorder of tendon sheath", "tendon sheath disease or disorder", "Tendon sheath disorder (disorder)", "disease or disorder of tendon sheath"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tendon sheath disorder", "shortest_name_length": 21}
{"curie": "MONDO:0019993", "names": ["congenital RAS", "congenital renal artery stenosis", "Congenital renal artery stenosis", "stenosis; renal artery, congenital", "Congenital renovascular hypoplasia", "congenital renovascular hypoplasia", "stenosis; artery, renal, congenital", "Congenital renal artery stenosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital renal artery stenosis", "shortest_name_length": 14}
{"curie": "UMLS:C5237189", "names": ["Advanced Pancreatic Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Pancreatic Neuroendocrine Neoplasm", "shortest_name_length": 43}
{"curie": "UMLS:C1096494", "names": ["Gastroduodenal bleeding", "Gastroduodenal hemorrhage", "Gastroduodenal haemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastroduodenal hemorrhage", "shortest_name_length": 23}
{"curie": "UMLS:C2826599", "names": ["Focal Mammary Duct Ectasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Focal Mammary Duct Ectasia", "shortest_name_length": 26}
{"curie": "MONDO:0010010", "names": ["SGS", "Sgs", "Schinzel Giedion syndrome", "Schinzel-Giedion syndrome", "Schinzel-Giedion Syndrome", "Schinzel-Giedion syndrome (SGS)", "Schinzel-Giedion syndrome (disorder)", "SCHINZEL-GIEDION MIDFACE RETRACTION SYNDROME", "Schinzel-Giedion Midface Retraction Syndrome", "Schinzel-Giedion midface retraction syndrome", "Schinzel-Giedion Midface-Retraction Syndrome", "Schinzel Giedion midface-retraction syndrome", "Schinzel-Giedion midface-retraction syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Schinzel-Giedion syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C5556342", "names": ["Refractory Thyroid Gland Medullary Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Thyroid Gland Medullary Carcinoma", "shortest_name_length": 44}
{"curie": "MONDO:0005966", "names": ["spleen tumor", "Splenic tumor", "Spleen Cancer", "spleen tumour", "tumour spleen", "spleen cancer", "cancer spleen", "spleen tumors", "splenic cancer", "Spleen--Cancer", "Spleen Cancers", "Spleen--Tumors", "spleen tumours", "Cancer, Spleen", "Splenic Cancer", "Cancer, Splenic", "spleen neoplasm", "Splenic Cancers", "Cancers, Spleen", "Tumor of spleen", "Spleen Neoplasm", "spleen neoplasms", "Neoplasm, Spleen", "cancer of spleen", "Spleen Neoplasms", "Cancers, Splenic", "Splenic neoplasm", "Cancer of Spleen", "Splenic Neoplasm", "splenic neoplasm", "Tumour of spleen", "Neoplasm, Splenic", "Neoplasms, Spleen", "Splenic Neoplasms", "Neoplasm of spleen", "neoplasm of spleen", "Neoplasms, Splenic", "cancer of the spleen", "Cancer of the Spleen", "Neoplasm malig;spleen", "malignant splenic tumor", "malignant Splenic tumor", "Malignant Splenic Tumor", "Malignant tumor of spleen", "malignant tumor of spleen", "malignant spleen neoplasm", "Malignant Tumor of Spleen", "malignant splenic neoplasm", "malignant tumour of spleen", "Malignant tumour of spleen", "Malignant Splenic Neoplasm", "Malignant splenic neoplasm", "Malignant Neoplasm of Spleen", "Malignant neoplasm of spleen", "malignant neoplasm of spleen", "Malignant Tumor of the Spleen", "Neoplasm of spleen (disorder)", "malignant tumor of the spleen", "neoplasm of spleen (diagnosis)", "malignant neoplasm of the spleen", "Malignant Neoplasm of the Spleen", "malignant neosplasm of the spleen", "Malignant tumor of spleen (disorder)", "malignant neoplasm of spleen (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spleen cancer", "shortest_name_length": 12}
{"curie": "UMLS:C5420194", "names": ["Laryngeal Soft Tissue Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laryngeal Soft Tissue Sarcoma", "shortest_name_length": 29}
{"curie": "MONDO:0017146", "names": ["sickle cell disease and related diseases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sickle cell disease and related diseases", "shortest_name_length": 40}
{"curie": "UMLS:C4688435", "names": ["Mantle Cell Lymphoma by Ann Arbor Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mantle Cell Lymphoma by Ann Arbor Stage", "shortest_name_length": 39}
{"curie": "MONDO:0002407", "names": ["spider nevi", "Spider nevi", "SPIDER NEVI", "SPIDER NAEVI", "spider nevus", "Spider Nevus", "spider naevi", "nevis spider", "Spider nevus", "Spider naevi", "Stellar nevus", "Nevus Araneus", "Nevus araneus", "spider naevus", "Nevus, spider", "Spider naevus", "Araneus nevus", "nevus; spider", "nevus araneus", "spider; nevus", "SPIDER ANGIOMA", "Nevus, stellar", "ANGIOMA SPIDER", "raspberry mark", "nevus; araneus", "Spider Angioma", "Mark;raspberry", "spider angioma", "Raspberry mark", "Nevus, araneus", "Angioma spider", "araneus; nevus", "Spider angioma", "spider; angioma", "angioma; spider", "STRAWBERRY MARK", "Strawberry mark", "Arterial spider", "mark strawberry", "nevus capillary", "Port wine stain", "Spider angiomas", "Vascular spider", "Strawberry nevi", "angiomas spider", "Mark;strawberry", "arterial spider", "vascular spider", "Capillary nevus", "Arterial Spider", "Vascular Spider", "strawberry mark", "arterial spiders", "spider; vascular", "strawberry nevus", "spiders vascular", "Strawberry Nevus", "nevus; capillary", "vascular; spider", "marks strawberry", "Capillary naevus", "Strawberry nevus", "capillary; nevus", "nevus; strawberry", "capillary angioma", "Strawberry naevus", "strawberry; nevus", "Angiomatous nevus", "Capillary angioma", "Capillary Angioma", "strawberry naevus", "nevus; angiomatous", "Hemangioma simplex", "strawberry angioma", "hemangioma simplex", "Strawberry angioma", "angiomatous; nevus", "angiomas capillary", "Angiomatous naevus", "Juvenile hemangioma", "angiomas strawberry", "simplex; hemangioma", "juvenile hemangioma", "Haemangioma simplex", "hemangioma; simplex", "juvenile; hemangioma", "infantile hemangioma", "hemangioma; juvenile", "Spider nevus of skin", "Strawberry birthmark", "Plexiform hemangioma", "plexiform hemangioma", "capillary hemangioma", "Telangiectatic nevus", "Infantile hemangioma", "strawberry birthmark", "Capillary hemangioma", "Juvenile haemangioma", "hemangioma capillary", "Capillary Hemangioma", "Telangiectatic Nevus", "Capillary haemangioma", "Plexiform haemangioma", "hemangioma; plexiform", "Capillary hemangiomas", "strawberry hemangioma", "hemangioma strawberry", "spider telangiectasis", "hemangioma; capillary", "spider telangiectasia", "Spider Telangiectasia", "infantile; hemangioma", "plexiform; hemangioma", "hemangiomas infantile", "Spider telangiectasia", "hemangioma; infantile", "Spider naevus of skin", "birthmarks strawberry", "Telangiectatic naevus", "capillary; hemangioma", "Capillary Hemangiomas", "Hemangioma, Capillary", "Nevus araneus of skin", "Spider Telangiectasis", "capillary hemangiomas", "capillary haemangioma", "Stellar nevus of skin", "Infantile haemangioma", "Spider angioma of skin", "Raspberry mark of skin", "Capillary hemangiomata", "spider nevus; vascular", "nevus; stellar angioma", "Hemangiomas, Capillary", "Skin Spider Angioma(s)", "Nevus telangiectaticus", "strawberry haemangioma", "Stellar naevus of skin", "vascular; spider nevus", "Naevus araneus of skin", "Strawberry haemangioma", "hemangiomas strawberry", "spider telangiectasias", "Strawberry mark of skin", "Vascular spider of skin", "stellate telangiectasis", "Spider nevus (disorder)", "Stellate Telangiectasis", "Arterial spider of skin", "Capillary nevus of skin", "Capillary naevus of skin", "Strawberry nevus of skin", "strawberry nevus of skin", "Congenital vascular nevus", "Strawberry naevus of skin", "Angiomatous nevus of skin", "Angiomatous naevus of skin", "Congenital vascular naevus", "congenital vascular naevus", "Nevus arachnoideus of skin", "Naevus arachnoideus of skin", "Capillary hemangioma of skin", "spider nevus; telangiectasia", "telangiectasia; spider nevus", "strawberry nevus (diagnosis)", "Strawberry hemangioma of skin", "strawberry nevus was observed", "Congenital vascular hamartoma", "Spider telangiectasis of skin", "Capillary haemangioma of skin", "Strawberry nevus of skin, NOS", "congenital vascular hamartoma", "cellular hemangioma of infancy", "Strawberry naevus of skin, NOS", "cellular hemangioma of Infancy", "Strawberry haemangioma of skin", "Capillary hemangioma (disorder)", "spider nevus (physical finding)", "Superficial infantile hemangioma", "Superficial infantile haemangioma", "strawberry nevus (physical finding)", "Strawberry nevus of skin (disorder)", "Congenital vascular nevus (disorder)", "capillary hemangioma (physical finding)", "Spider telangiectasis of skin (disorder)", "capillary hemangioma (morphologic abnormality)", "Capillary hemangioma (morphologic abnormality)", "cellular hemangioma of infancy (strawberry nevus)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "capillary hemangioma", "shortest_name_length": 11}
{"curie": "MONDO:0005920", "names": ["malaria; tropica", "Malaria subtertian", "Falciparum Malaria", "Falciparum malaria", "malaria falciparum", "Pernicious malaria", "Subtertian malaria", "falciparum malaria", "malaria; malignant", "malignant; malarial", "Malaria, falciparum", "malaria; subtertian", "Malaria, Falciparum", "falciparum; malarial", "subtertian; malarial", "Plasmodium; falciparum", "Malignant tertian fever", "ST - Subtertian malaria", "malignant tertian fever", "STM - Subtertian malaria", "estivo-autumnal; malaria", "malaria; estivo-autumnal", "Malignant tertian malaria", "malaria fever, subtertian", "Malaria fever, subtertian", "malaria; tertian, malignant", "Falciparum malaria (disorder)", "plasmodium falciparum malaria", "Plasmodium falciparum malaria", "Plasmodium falciparum Malaria", "MT - Malignant tertian malaria", "Falciparum malaria - malignant", "malaria; Plasmodium falciparum", "Malaria, Plasmodium falciparum", "MTM - Malignant tertian malaria", "Malaria by Plasmodium falciparum", "Malignant tertian fever (finding)", "malignant tertian fever (finding)", "falciparum malaria [malignant tertian]", "Malaria fever by Plasmodium falciparum", "Falciparum malaria (malignant tertian)", "Falciparum malaria [malignant tertian]", "Plasmodium falciparum malaria (diagnosis)", "Plasmodium falciparum malaria, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Plasmodium falciparum malaria", "shortest_name_length": 16}
{"curie": "UMLS:C4317171", "names": ["Adolescent Obesity", "Adolescent obesity", "Obesity, Adolescent", "Obesity in adolescence", "Obesity in Adolescence", "Obesity in adolescence (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adolescent Obesity", "shortest_name_length": 18}
{"curie": "MONDO:0011339", "names": ["SPG8", "Spg 8", "spastic paraplegia 8", "Spastic Paraplegia 8", "Spastic Paraplegia Type 8", "Hereditary Spastic Paraplegia 8", "hereditary spastic paraplegia 8", "WASHC5 hereditary spastic paraplegia", "hereditary spastic paraplegia type 8", "autosomal dominant spastic paraplegia 8", "Autosomal Dominant Spastic Paraplegia 8", "Spastic paraplegia 8, autosomal dominant", "SPASTIC PARAPLEGIA 8, AUTOSOMAL DOMINANT", "spastic paraplegia 8, autosomal dominant", "Autosomal dominant spastic paraplegia type 8", "autosomal dominant spastic paraplegia type 8", "Autosomal dominant spastic paraplegia type 8 (disorder)", "hereditary spastic paraplegia caused by mutation in WASHC5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 8", "shortest_name_length": 4}
{"curie": "MONDO:0020974", "names": ["Larynx Granuloma", "Larynx Granulomas", "granuloma; larynx", "larynx; granuloma", "Laryngeal granuloma", "laryngeal granuloma", "Granuloma of Larynx", "Laryngeal Granuloma", "Laryngeal Granulomas", "Granuloma, Laryngeal", "Granulomas, Laryngeal", "Laryngeal granuloma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laryngeal granuloma", "shortest_name_length": 16}
{"curie": "UMLS:C4726621", "names": ["Refractory Primary Peritoneal Cancer", "Refractory Primary Peritoneal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Primary Peritoneal Carcinoma", "shortest_name_length": 36}
{"curie": "MONDO:0012791", "names": ["MTDPS5", "encephalomyopathy", "Booth Haworth Dilling syndrome", "booth-Haworth-Dilling syndrome", "Booth-Haworth-Dilling syndrome", "Succinate-Coa Ligase Deficiency", "succinate-CoA ligase deficiency", "Succinate-Coenzyme A Ligase Deficiency", "mitochondrial DNA depletion syndrome 5", "mitochondrial DNA depletion syndrome type 5", "mitochondrial encephalomyopathy aminoacidopathy", "Mitochondrial encephalomyopathy-aminoacidopathy syndrome", "Mitochondrial encephalomyopathy aminoacidopathy syndrome", "mitochondrial encephalomyopathy-aminoacidopathy syndrome", "mtDNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria", "Mitochondrial Dna Depletion, Encephalomyopathic Form, with Methylmalonic Aciduria", "Mitochondrial DNA depletion syndrome encephalomyopathic form with methylmalonic aciduria", "Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria", "mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria", "Mitochondrial Dna Depletion Syndrome, Encephalomyopathic Form, with Mild Methylmalonic Aciduria", "mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)", "MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)", "Mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form with methylmalonic aciduria", "mitochondrial dna depletion syndrome, encephalomyopathic form with methylmalonic aciduria, autosomal recessive", "Mitochondrial Dna Depletion Syndrome, Encephalomyopathic Form, With Methylmalonic Aciduria, Autosomal Recessive", "mtDNA (mitochondrial deoxyribonucleic acid) depletion syndrome encephalomyopathic form with methylmalonic aciduria", "Mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form with methylmalonic aciduria (disorder)", "MITOCHONDRIAL DNA DEPLETION SYNDROME, ENCEPHALOMYOPATHIC FORM, WITH OR WITHOUT METHYLMALONIC ACIDURIA, AUTOSOMAL RECESSIVE, SUCLA2-RELATED", "mitochondrial DNA depletion syndrome, encephalomyopathic form, with or without methylmalonic aciduria, autosomal recessive, Sucla2-related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria", "shortest_name_length": 6}
{"curie": "MONDO:0006612", "names": ["steroid lipomatosis", "Steroid Lipomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "steroid lipomatosis", "shortest_name_length": 19}
{"curie": "MONDO:0013459", "names": ["OI10", "OI type X", "OI, TYPE X", "OI type 10", "OI, type 10", "osteogenesis imperfecta type X", "osteogenesis imperfecta type 10", "osteogenesis imperfecta, type X", "OSTEOGENESIS IMPERFECTA, TYPE X", "SERPINH1 osteogenesis imperfecta", "osteogenesis imperfecta, type 10", "osteogenesis imperfecta caused by mutation in SERPINH1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteogenesis imperfecta type 10", "shortest_name_length": 4}
{"curie": "MONDO:0016822", "names": ["myalgia-eosinophilia syndrome associated with tryptophan"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myalgia-eosinophilia syndrome associated with tryptophan", "shortest_name_length": 56}
{"curie": "MONDO:0010632", "names": ["DEE1", "ISSX1", "EIEE1", "XMESID", "West syndrome, X-linked", "Ohtahara syndrome, X-linked", "X-linked infantile spasm syndrome 1", "infantile spasm syndrome, X-linked 1", "Infantile Spasm Syndrome, X-Linked 1", "INFANTILE SPASM SYNDROME, X-LINKED 1", "Early Infantile Epileptic Encephalopathy 1", "early infantile epileptic encephalopathy 1", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1", "Developmental and Epileptic Encephalopathy 1", "Epileptic Encephalopathy, Early Infantile, 1", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 1", "ARX early infantile epileptic encephalopathy", "epileptic encephalopathy, early infantile, 1", "developmental and epileptic encephalopathy 1", "arx early infantile epileptic encephalopathy", "infantile epileptic-dyskinetic encephalopathy", "developmental and epileptic encephalopathy, 1", "epileptic encephalopathy, early infantile, type 1", "developmental and epileptic encephalopathy 1, X-linked recessive", "early infantile epileptic encephalopathy caused by mutation in ARX", "early infantile epileptic encephalopathy caused by mutation in arx"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 1", "shortest_name_length": 4}
{"curie": "MONDO:0023133", "names": ["Faye-Petersen-Ward-Carey syndrome", "Faye-Petersen Ward Carey syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Faye-Petersen-Ward-Carey syndrome", "shortest_name_length": 33}
{"curie": "MONDO:0100092", "names": ["MYOCL2", "MYOCLONUS, FAMILIAL, 2", "myoclonus, familial, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myoclonus, familial, 2", "shortest_name_length": 6}
{"curie": "MONDO:0012561", "names": ["CAKUT1", "RHDNS1", "renal hypodysplasia, nonsyndromic, 1", "RENAL HYPODYSPLASIA, NONSYNDROMIC, 1", "Renal Hypodysplasia, Nonsyndromic, 1", "CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 1", "congenital anomalies of kidney and urinary tract 1", "DSTYK congenital anomaly of kidney and urinary tract", "Congenital anomalies of the kidney and urinary tract 1", "congenital anomaly of kidney and urinary tract caused by mutation in DSTYK"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital anomalies of kidney and urinary tract 1", "shortest_name_length": 6}
{"curie": "UMLS:C3899649", "names": ["Oligoastrocytoma", "childhood oligoastrocytoma", "Childhood Oligoastrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Oligoastrocytoma", "shortest_name_length": 16}
{"curie": "MONDO:0000492", "names": ["chronic insufficiency venou", "Chronic venous insufficiency", "chronic venous insufficiency", "Chronic venous insufficiency NOS", "Chronic venous insufficiency, NOS", "chronic venous insufficiency (disease)", "venous insufficiency (disease), chronic", "chronic peripheral venous insufficiency", "Venous insufficiency (chronic)(peripheral)", "Venous insufficiency (chronic) (peripheral)", "chronic peripheral venous insufficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic venous insufficiency", "shortest_name_length": 27}
{"curie": "UMLS:C0235214", "names": ["EJACULATION INHIBITED", "Ejaculation inhibited", "ejaculation inhibited", "inhibited ejaculation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ejaculation inhibited", "shortest_name_length": 21}
{"curie": "UMLS:C1336026", "names": ["Solid adenocarcinoma", "Solid Lung Adenocarcinoma", "Lung Solid Adenocarcinoma with Mucin", "Solid Adenocarcinoma of Lung with Mucin", "Pulmonary Solid Adenocarcinoma with Mucin", "Solid Adenocarcinoma of the Lung with Mucin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Solid Lung Adenocarcinoma", "shortest_name_length": 20}
{"curie": "MONDO:0015241", "names": ["Kuskokwim disease", "Kuskokwim syndrome", "arthrogryposis like disorder", "arthrogryposis-like syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis-like syndrome", "shortest_name_length": 17}
{"curie": "UMLS:C0151759", "names": ["Genital leukoplakia", "Leukoplakia genital", "LEUKOPLAKIA GENITAL", "Genital Leukoplakia", "GENITAL LEUKOPLAKIA", "Leukoplakia of Genitals", "Leukoplakia of the Genitals"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Genital leukoplakia", "shortest_name_length": 19}
{"curie": "UMLS:C4553886", "names": ["Stage I Adrenal Cortex Cancer", "stage I adrenocortical cancer", "stage I adrenal cortex carcinoma", "stage I adrenocortical carcinoma", "adrenocortical carcinoma, stage I", "carcinoma, adrenocortical stage I", "stage I adrenal cortex carcinoma AJCC v8", "Stage I Adrenal Cortex Carcinoma AJCC v8", "Stage I Adrenal Cortical Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Adrenal Cortex Carcinoma AJCC v8", "shortest_name_length": 29}
{"curie": "MONDO:0044993", "names": ["Sympathetic Disorder", "sympathetic disorder", "disorder; sympathetic", "sympathetic; disorder", "disorders sympathetic", "sympathetic nervous system disease", "Sympathetic Nervous System Diseases", "sympathetic nervous system disorder", "Nervous System Diseases, Sympathetic", "nervous system; disorder, sympathetic", "disease of sympathetic nervous system", "sympathetic; nervous system, disorder", "disorder of sympathetic nervous system", "Disorder of sympathetic nervous system", "Disorder of sympathetic nervous system, NOS", "sympathetic nervous system disease or disorder", "disease (or disorder); sympathetic nervous system", "Disorder of sympathetic nervous system (disorder)", "disease or disorder of sympathetic nervous system", "disease (or disorder); nervous system, sympathetic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sympathetic nervous system disorder", "shortest_name_length": 20}
{"curie": "UMLS:C4744559", "names": ["Metastatic Oral Cavity Adenoid Cystic Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Oral Cavity Adenoid Cystic Carcinoma", "shortest_name_length": 47}
{"curie": "MONDO:0002821", "names": ["wuchernde Struma Langhans", "Wuchernde Struma Langhans", "Langhans; wuchernde Struma", "Trabecular Follicular carcinoma", "trabecular follicular carcinoma", "Follicular carcinoma, trabecular", "carcinoma; trabecular, follicular", "carcinoma; follicular, trabecular", "follicular; carcinoma, trabecular", "Follicular carcinoma - trabecular", "trabecular follicular adenocarcinoma", "Follicular carcinoma, trabecular type", "trabecular; follicular adenocarcinoma", "follicular adenocarcinoma, trabecular", "Follicular adenocarcinoma, trabecular", "adenocarcinoma; trabecular follicular", "Follicular adenocarcinoma - trabecular", "adenocarcinoma; follicular, trabecular", "follicular; adenocarcinoma, trabecular", "Follicular adenocarcinoma, trabecular type", "Follicular carcinoma, moderately differentiated", "Follicular carcinoma - moderately differentiated", "Follicular carcinoma, moderately differentiated type", "Follicular adenocarcinoma, moderately differentiated", "Follicular adenocarcinoma - moderately differentiated", "Follicular adenocarcinoma, moderately differentiated type", "Solid/Trabecular Variant Thyroid Gland Papillary Carcinoma", "Follicular adenocarcinoma, trabecular (morphologic abnormality)", "follicular adenocarcinoma, trabecular (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trabecular follicular adenocarcinoma", "shortest_name_length": 25}
{"curie": "UMLS:C1377828", "names": ["POA", "Paraneoplastic Opsoclonus Ataxia", "Paraneoplastic Opsoclonus-Ataxia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paraneoplastic Opsoclonus Ataxia", "shortest_name_length": 3}
{"curie": "UMLS:C4683521", "names": ["Adrenal Cortex Carcinoma by AJCC v8 Stage", "Adrenal Cortical Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adrenal Cortical Carcinoma by AJCC v8 Stage", "shortest_name_length": 41}
{"curie": "MONDO:0002014", "names": ["Ehlers-Danlos syndrome, recessive type 4", "Ehlers-Danlos syndrome, recessive type IV", "Ehlers-Danlos syndrome type IV recessive type", "autosomal recessive type IV Ehlers-Danlos syndrome", "Ehlers-Danlos syndrome, recessive type IV (diagnosis)", "autosomal recessive Ehlers-Danlos syndrome, vascular type", "Ehlers-Danlos syndrome, vascular type, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive Ehlers-Danlos syndrome, vascular type", "shortest_name_length": 40}
{"curie": "MONDO:0010625", "names": ["GPL115 DEFICIENCY", "Gpl115 deficiency", "Gpl115 Deficiency", "IMMUNODEFICIENCY, X-LINKED, WITH DEFICIENCY OF 115,000 DALTON SURFACE GLYCOPROTEIN", "immunodeficiency, X-linked, with deficiency of 115,000 Dalton surface glycoprotein", "Immunodeficiency, X-Linked, with Deficiency of 115,000 Dalton Surface Glycoprotein"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency, X-linked, with deficiency of 115,000 Dalton surface glycoprotein", "shortest_name_length": 17}
{"curie": "MONDO:0012605", "names": ["MCOP5", "isolated microphthalmia 5", "microphthalmia, isolated 5", "MICROPHTHALMIA, ISOLATED 5", "MFRP isolated microphthalmia", "isolated microphthalmia type 5", "microphthalmia, isolated type 5", "isolated microphthalmia caused by mutation in MFRP", "Nanophtalmos-retinitis pigmentosa-foveoschisis-optic disc drusen syndrome", "microphthalmia-retinitis pigmentosa-foveoschisis-optic disc drusen syndrome", "posterior microphthalmia with retinitis pigmentosa, foveoschisis and optic disc drusen", "microphthalmia, posterior, with retinitis pigmentosa, foveoschisis, and optic Disc drusen", "MICROPHTHALMIA, POSTERIOR, WITH RETINITIS PIGMENTOSA, FOVEOSCHISIS, AND OPTIC DISC DRUSEN", "Microphthalmia, Posterior, With Retinitis Pigmentosa, Foveoschisis, And Optic Disk Drusen", "Microphthalmia, Posterior, With Retinitis Pigmentosa, Foveoschisis, And Optic Disc Drusen"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated microphthalmia 5", "shortest_name_length": 5}
{"curie": "MONDO:0035350", "names": ["letrozole toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "letrozole toxicity", "shortest_name_length": 18}
{"curie": "UMLS:C1336161", "names": ["fallopian tube cancer stage IIA", "Fallopian Tube Cancer Stage IIA", "Stage IIA Fallopian Tube Cancer", "stage IIA fallopian tube cancer", "AJCC Stage IIA Fallopian Tube Cancer", "AJCC stage IIA fallopian tube cancer", "stage IIA fallopian tube cancer AJCC v6", "FIGO stage IIA fallopian tube carcinoma", "Stage IIA Fallopian Tube Cancer AJCC v6", "FIGO Stage IIA Fallopian Tube Carcinoma", "Stage IIA Fallopian Tube Cancer AJCC v7", "stage IIA fallopian tube cancer AJCC v7", "FIGO stage IIA carcinoma of fallopian tube", "FIGO Stage IIA Carcinoma of Fallopian Tube", "Stage IIA Fallopian Tube Cancer AJCC v6 and v7", "FIGO Stage IIA Carcinoma of the Fallopian Tube", "FIGO stage IIA carcinoma of the fallopian tube"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Fallopian Tube Cancer AJCC v6 and v7", "shortest_name_length": 31}
{"curie": "MONDO:0005085", "names": ["eye web", "Web eye", "eye webs", "Pterygia", "eyes webs", "pterygium", "Pterygium", "PTERYGIUM", "Pterygiums", "pterygiums", "eye webbed", "eye webbing", "surfer's eye", "Surfer's eye", "pterygium eye", "pterygium nos", "eye pterygium", "Pterygium, NOS", "Pterygium of eye", "Corneal pterygium", "Pterygium (disorder)", "pterygium (diagnosis)", "Pterygium, unspecified", "conjunctival pterygium", "Wing-shaped conjunctiva", "Unspecified pterygium of eye", "pterygium (physical finding)", "pterygium of conjunctiva and cornea", "Pterygium of Conjunctiva and Cornea", "Unspecified pterygium of unspecified eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pterygium", "shortest_name_length": 7}
{"curie": "MONDO:0023599", "names": ["Mesomelic dwarf", "Dwarf, mesomelic", "mesomelic dysplasia", "Mesomelic dysplasia", "Mesomelic Dysplasia", "mesomelic dysplasias", "Mesomelic Dysplasias", "Mesomelic dysplasia (disorder)", "mesomelic dysplasia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mesomelic dysplasia", "shortest_name_length": 15}
{"curie": "MONDO:0023013", "names": ["Duker Weiss Siber syndrome", "Duker-Weiss-Siber syndrome", "microphthalmos, microencephaly, mental retardation, agenesis of the corpus callosum, hypospadius, and cryptorchidism", "microphthalmos, microencephaly, intellectual disability, agenesis of the corpus callosum, hypospadius, and cryptorchidism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Duker-Weiss-Siber syndrome", "shortest_name_length": 26}
{"curie": "MONDO:0017617", "names": ["adult acquired immunodeficiency", "acquired immunodeficiency of adults", "anti-IFN-gamma autoantibody syndrome", "acquired adult-onset immunodeficiency", "adult onset immunodeficiency syndrome", "adult-onset immunodeficiency due to anti-interferon-gamma autoantibody", "adult-onset immunodeficiency with anti-interferon-gamma autoantibodies", "adult-onset immunodeficiency with acquired Anti-interferon-gamma autoantibodies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired adult-onset immunodeficiency", "shortest_name_length": 31}
{"curie": "MONDO:0002755", "names": ["SPB", "SOM disease", "Monostotic myeloma", "Solitary osseous myeloma", "Bone Solitary Plasmacytoma", "Isolated osseous plasmacytoma", "Solitary Plasmacytoma of Bone", "Solitary Osseous Plasmacytoma", "solitary plasmacytoma of bone", "isolated osseous plasmacytoma", "solitary osseous plasmacytoma", "isolated plasmacytoma of bone", "Solitary plasmacytoma of bone", "Primary plasmacytoma of the bone", "Solitary osseous myeloma (disorder)", "Solitary osseous myeloma (diagnosis)", "malignant neoplasm solitary osseous myeloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "solitary osseous plasmacytoma", "shortest_name_length": 3}
{"curie": "UMLS:C0235325", "names": ["gastric bleed", "Gastrorrhagia", "gastrorrhagia", "bleeds gastric", "GASTRIC BLEEDING", "Gastric bleeding", "gastric bleeding", "bleeding gastric", "GASTRIC HEMORRHAGE", "Hemorrhage stomach", "gastric hemorrhage", "Gastric Hemorrhage", "stomach hemorrhage", "HEMORRHAGE GASTRIC", "Hemorrhage gastric", "HEMORRHAGE STOMACH", "Stomach hemorrhage", "STOMACH HEMORRHAGE", "Gastric hemorrhage", "stomach; hemorrhage", "hemorrhage; stomach", "Haemorrhage stomach", "Stomach haemorrhage", "HAEMORRHAGE GASTRIC", "Haemorrhage gastric", "Gastric haemorrhage", "Gastric bleeding, NOS", "Gastric hemorrhage NOS", "Gastric hemorrhage, NOS", "Gastric haemorrhage, NOS", "gastric bleeding (diagnosis)", "Gastric hemorrhage (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric hemorrhage", "shortest_name_length": 13}
{"curie": "MONDO:0013199", "names": ["TSC2", "tuberous sclerosis-2", "tuberous sclerosis 2", "Tuberous Sclerosis 2", "TUBEROUS SCLEROSIS 2", "tuberous sclerosis type 2", "tuberous sclerosis, type 2", "TUBEROUS SCLEROSIS 2 (disorder)", "Tsc2 Angiomyolipomas, Renal, Modifier Of", "TSC2 Angiomyolipomas, renal, modifier of", "TSC2 ANGIOMYOLIPOMAS, RENAL, MODIFIER OF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tuberous sclerosis 2", "shortest_name_length": 4}
{"curie": "MONDO:0001350", "names": ["parametrium cancer", "Cancer of parametrium", "cancer of parametrium", "malignant parametrium neoplasm", "malignant parametrial neoplasm", "parametrium malignant neoplasm", "malignant tumor of parametrium", "malignant neoplasm of parametrium", "Malignant neoplasm of parametrium", "Malignant neoplasm of parametrium (disorder)", "malignant neoplasm of parametrium (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parametrium malignant neoplasm", "shortest_name_length": 18}
{"curie": "MONDO:0031037", "names": ["CCM", "familial cerebral cavernoma", "Familial cerebral cavernoma", "cavernous angioma, familial", "Familial cavernous hemangioma", "hereditary cerebral cavernoma", "Hereditary cerebral cavernoma", "cerebral capillary malformations", "cerebral cavernous malformations", "familial brain cavernous angioma", "Familial brain cavernous angioma", "Hereditary brain cavernous angioma", "hereditary brain cavernous angioma", "cavernous angiomatous malformations", "Familial cerebral cavernous angioma", "familial brain cavernous hemangioma", "hereditary brain cavernous hemangioma", "familial cerebral cavernous malformation", "Familial cerebral cavernous malformation", "hereditary cavernous hemangioma of brain", "Hereditary cavernous hemangioma of brain", "cavernous malformations of CNS and retina", "Hereditary cavernous haemangioma of brain", "hereditary cerebral cavernous malformation", "Hereditary cerebral cavernous malformation", "famililal cerebral cavernous malformations", "Hereditary cavernous hemangioma of brain (disorder)", "hereditary cavernous hemangioma of brain (diagnosis)", "hyperkeratotic cutaneous capillary-Venous malformations associated with cerebral capillary malformations"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "famililal cerebral cavernous malformations", "shortest_name_length": 3}
{"curie": "MONDO:0013888", "names": ["ETM4", "essential tremor 4", "FUS essential tremor", "hereditary essential tremor 4", "tremor, hereditary essential, 4", "TREMOR, HEREDITARY ESSENTIAL, 4", "essential tremor, hereditary, 4", "tremor, hereditary essential, type 4", "essential tremor caused by mutation in FUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tremor, hereditary essential, 4", "shortest_name_length": 4}
{"curie": "MONDO:0004511", "names": ["Lower Clivus Meningioma", "lower clivus meningioma", "Meningioma of Lower Clivus", "meningioma of Lower clivus", "meningioma of the lower clivus", "Meningioma of the Lower Clivus", "meningioma of the lower Clivus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lower clivus meningioma", "shortest_name_length": 23}
{"curie": "MONDO:0008645", "names": ["Stoll Kieny Dott syndrome", "Stoll-Kieny-Dott syndrome", "Stoll Alembik Dott syndrome", "ventricular extrasystoles perodactyly Robin sequence", "Ventricular extrasystoles with syncope, perodactyly, and robin sequence", "ventricular extrasystoles with syncope, perodactyly, and ROBIN sequence", "VENTRICULAR EXTRASYSTOLES WITH SYNCOPE, PERODACTYLY, AND ROBIN SEQUENCE", "ventricular extrasystoles with syncopal episodes - perodactyly - Robin sequence", "Ventricular extrasystoles with syncope, perodactyly and Robin sequence syndrome", "Ventricular extrasystoles with syncopal episodes-perodactyly-Robin sequence syndrome", "ventricular extrasystoles with syncopal episodes-perodactyly-robin sequence syndrome", "Ventricular extrasystoles with syncope, perodactyly and Robin sequence syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ventricular extrasystoles with syncopal episodes-perodactyly-robin sequence syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0003028", "names": ["Thyroid Sarcoma", "thyroid sarcoma", "Sarcoma of Thyroid", "sarcoma of thyroid", "thyroid gland sarcoma", "Thyroid Gland Sarcoma", "sarcoma of the thyroid", "Sarcoma of the Thyroid", "sarcoma of thyroid gland", "Sarcoma of Thyroid Gland", "sarcoma of the Thyroid gland", "Sarcoma of the Thyroid Gland", "sarcoma of the thyroid gland", "sarcoma of thyroid gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid sarcoma", "shortest_name_length": 15}
{"curie": "MONDO:0030707", "names": ["Trichomonas balanoposthitis", "Trichomonas Balanoposthitis", "Trichomonal balanoposthitis", "Trichomonal balanoposthitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Trichomonas balanoposthitis", "shortest_name_length": 27}
{"curie": "MONDO:0020641", "names": ["Respiratory Neoplasm", "respiratory neoplasm", "Neoplasm;respiratory", "Neoplasm, Respiratory", "Respiratory Neoplasms", "respiratory tract tumor", "Respiratory system tumor", "Respiratory system tumour", "respiratory tract neoplasm", "tumor of respiratory tract", "Respiratory tract neoplasm", "Respiratory Tract Neoplasm", "Respiratory System Neoplasm", "neoplasm, respiratory tract", "respiratory system neoplasm", "neoplasm respiratory system", "Respiratory Tract Neoplasms", "tract neoplasm, respiratory", "Neoplasm, Respiratory Tract", "Respiratory tract neoplasms", "Tumor of respiratory system", "tract neoplasms, respiratory", "Respiratory System Neoplasms", "neoplasms, respiratory tract", "Neoplasm, Respiratory System", "Tumour of respiratory system", "neoplasm of respiratory tract", "Neoplasm of respiratory tract", "Neoplasm of respiratory system", "tumor of the respiratory tract", "Respiratory tract neoplasm NOS", "neoplasm of the respiratory tract", "Neoplasm of the respiratory system", "neoplasm of the respiratory system", "Neoplasm of respiratory tract (disorder)", "neoplasm of respiratory tract (diagnosis)", "Neoplasm of respiratory system (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "respiratory tract neoplasm", "shortest_name_length": 20}
{"curie": "MONDO:0012041", "names": ["MAP", "FAP2", "MAP syndrome", "MUTYH-related AFAP", "MYH-associated polyposis", "MYH-Associated Polyposis", "MUTYH-Associate Polyposis", "MUTYH-Associated Polyposis", "MUTYH-associated polyposis", "MUTYH-related attenuated FAP", "familial adenomatous polyposis 2", "FAMILIAL ADENOMATOUS POLYPOSIS 2", "familial adenomatous polyposis, 2", "familial adenomatous polyposis, type 2", "autosomal recessive multiple colorectal adenomas", "MUTYH-related attenuated familial polyposis coli", "autosomal recessive familial adenomatous polyposis", "Adenomas, Multiple Colorectal, Autosomal Recessive", "ADENOMAS, MULTIPLE COLORECTAL, AUTOSOMAL RECESSIVE", "adenomas, multiple colorectal, autosomal recessive", "colorectal adenomatous polyposis, autosomal recessive", "COLORECTAL ADENOMATOUS POLYPOSIS, AUTOSOMAL RECESSIVE", "Colorectal Adenomatous Polyposis, Autosomal Recessive", "MUTYH-related attenuated familial adenomatous polyposis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial adenomatous polyposis 2", "shortest_name_length": 3}
{"curie": "MONDO:0060455", "names": ["HACXL", "X-linked congenital hemolytic anemia", "HEMOLYTIC ANEMIA, CONGENITAL, X-LINKED", "hemolytic anemia, congenital, X-linked", "hemolytic anemia, congenital, X-linked, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked congenital hemolytic anemia", "shortest_name_length": 5}
{"curie": "UMLS:C0750953", "names": ["Bladder Neurogenesis", "Neurogenesis, Bladder", "Urinary Bladder Neurogenesis", "Neurogenesis, Urinary Bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urinary Bladder Neurogenesis", "shortest_name_length": 20}
{"curie": "MONDO:0013927", "names": ["CG3", "PBD3A", "peroxisome biogenesis disorder 3A", "Peroxisome Biogenesis Disorder 3A", "peroxisome biogenesis disorder 3A (Zellweger)", "PEROXISOME BIOGENESIS DISORDER 3A (ZELLWEGER)", "Peroxisome Biogenesis Disorder, Complementation Group 3", "PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 3", "peroxisome biogenesis disorder, complementation group 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder 3A (Zellweger)", "shortest_name_length": 3}
{"curie": "UMLS:C0586371", "names": ["Mild Rectal Dysplasia", "Mild dysplasia of rectum", "Mild Dysplasia of Rectum", "Mild Dysplasia of the Rectum", "Mild dysplasia of rectum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mild dysplasia of rectum", "shortest_name_length": 21}
{"curie": "MONDO:0021022", "names": ["STHE", "KOK DISEASE", "Kok disease", "hyperekplexia", "startle disease", "Stiff baby syndrome", "STIFF-BABY SYNDROME", "hereditary hyperexplexia", "familial startle disease", "Familial startle disease", "hereditary hyperekplexia", "Hereditary Hyperexplexia", "Hereditary hyperexplexia", "hyperexplexia hereditary", "Hereditary hyperekplexia", "Hyperexplexia hereditary", "STARTLE DISEASE, FAMILIAL", "Exagerrated startle reflex", "EXAGGERATED STARTLE REACTION", "Congenital stiff man syndrome", "congenital stiff man syndrome", "STARTLE REACTION, EXAGGERATED", "STIFF-MAN SYNDROME, CONGENITAL", "Congenital stiff person syndrome", "STIFF-PERSON SYNDROME, CONGENITAL", "Hereditary hyperekplexia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary hyperekplexia", "shortest_name_length": 4}
{"curie": "UMLS:C2825306", "names": ["Therapy Related Leukemia", "Therapy-Related Leukemia", "Treatment Induced Leukemia", "Treatment related leukemia", "Treatment Related Leukemia", "Treatment related leukaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Treatment related leukaemia", "shortest_name_length": 24}
{"curie": "MONDO:0008264", "names": ["MCKD", "ADTKD", "medullary cystic disease", "medullary cystic kidney disease", "Medullary cystic kidney disease", "Medullary cystic kidney disease 1", "polycystic kidneys, medullary type", "Medullary Cystic Kidney Disease Type I", "Familial juvenile hyperuricemic nephropathy", "autosomal dominant interstitial kidney disease", "Autosomal dominant medullary cystic kidney disease", "autosomal dominant medullary cystic kidney disease", "autosomal dominant tubulointerstitial kidney disease", "Autosomal dominant tubulointerstitial kidney disease", "Autosomal dominant tubulointerstitial kidney disease (disorder)", "autosomal dominant medullary cystic kidney disease with or without hyperuricemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant medullary cystic kidney disease with or without hyperuricemia", "shortest_name_length": 4}
{"curie": "MONDO:0008127", "names": ["OMM syndrome", "OMM SYNDROME", "Pillay syndrome", "Ophthalmomandibulomelic dysplasia", "ophthalmomandibulomelic dysplasia", "Ophthalmomandibulomelic Dysplasia", "OPHTHALMOMANDIBULOMELIC DYSPLASIA", "Ophthalmo-mandibulo-melic dysplasia", "OMM (ophthalmomandibulomelic) syndrome", "Ophthalmomandibulomelic dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ophthalmomandibulomelic dysplasia", "shortest_name_length": 12}
{"curie": "UMLS:C5420144", "names": ["Microsatellite Stable Colorectal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Microsatellite Stable Colorectal Carcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0017420", "names": ["intercalary meromelia", "intercalary limb defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intercalary limb defects", "shortest_name_length": 21}
{"curie": "DOID:0080708", "names": ["Medulloblastoma, group 4", "medulloblastoma non-WNT/non-SHH group 4", "Medulloblastoma, Non-WNT/Non-SHH, Group 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "medulloblastoma non-WNT/non-SHH group 4", "shortest_name_length": 24}
{"curie": "MONDO:0012162", "names": ["MDPT2", "patterned macular dystrophy 2", "macular dystrophy, patterned, 2", "MACULAR DYSTROPHY, PATTERNED, 2", "CTNNA1 patterned macular dystrophy", "patterned macular dystrophy type 2", "macular dystrophy, patterned, type 2", "butterfly-shaped pigmentary maculary dystrophy 2", "macular dystrophy, butterfly-Shaped pigmentary, 2", "MACULAR DYSTROPHY, BUTTERFLY-SHAPED PIGMENTARY, 2", "Macular Dystrophy, Butterfly-Shaped Pigmentary, 2", "patterned macular dystrophy caused by mutation in CTNNA1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "patterned macular dystrophy 2", "shortest_name_length": 5}
{"curie": "UMLS:C1708498", "names": ["Indirect Contact Transmission Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Indirect Contact Transmission Infection", "shortest_name_length": 39}
{"curie": "UMLS:C1336520", "names": ["Submaxillary Gland Acinic Cell Carcinoma", "Submandibular Gland Acinic Cell Carcinoma", "Acinic Cell Carcinoma of Submaxillary Gland", "Acinic Cell Carcinoma of Submandibular Gland", "Acinic Cell Carcinoma of the Submaxillary Gland", "Acinic Cell Carcinoma of the Submandibular Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Submandibular Gland Acinic Cell Carcinoma", "shortest_name_length": 40}
{"curie": "UMLS:C5418911", "names": ["Advanced Malignant Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Malignant Germ Cell Tumor", "shortest_name_length": 34}
{"curie": "MONDO:0009543", "names": ["MacDermot Winter syndrome", "MacDermot-Winter syndrome", "MACDERMOT-WINTER SYNDROME", "Mac Dermot Winter syndrome", "Prominent glabella microcephaly hypogenitalism", "prominent glabella microcephaly hypogenitalism", "Prominent glabella-microcephaly-hypogenitalism syndrome", "prominent glabella-microcephaly-hypogenitalism syndrome", "Prominent glabella with microcephaly and hypogenitalism syndrome", "Prominent glabella with microcephaly and hypogenitalism syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prominent glabella-microcephaly-hypogenitalism syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0025152", "names": ["Ape Disease", "ape disease", "disease, ape", "Disease, Ape", "Ape Diseases", "diseases, ape", "Diseases, Ape", "Pongidae Disease", "Pongidae disease", "Pongidae diseases", "disease, Pongidae", "Pongidae Diseases", "Disease, Pongidae", "Diseases, Pongidae", "diseases, Pongidae", "non-human ape disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-human ape disease", "shortest_name_length": 11}
{"curie": "UMLS:C1697746", "names": ["rectal obstruction", "Rectal Obstruction", "Rectal obstruction", "rectum; obstruction", "obstruction; rectum", "rectal obstruction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rectal Obstruction", "shortest_name_length": 18}
{"curie": "MONDO:0004880", "names": ["Bowel dysfunction", "bowel dysfunction", "BD - Bowel dysfunction", "FUNCTIONAL BOWEL DISORDER", "functional bowel disorder", "bowel disorders functional", "Bowel dysfunction (disorder)", "Bowel dysfunction (diagnosis)", "lower digestive tract disease", "Intestinal functional disorder", "FUNCTIONAL INTESTINAL DISORDER", "intestine; disease, functional", "disease of lower digestive tract", "Functional disorder of intestine", "functional disorder of intestine", "Intestinal functional disorder NOS", "intestinal disorder bowel dysfunction", "Functional disorder of intestine, NOS", "Functional disorder of intestine (disorder)", "Functional intestinal disorder, unspecified", "functional disorder of intestine (diagnosis)", "Unspecified functional disorder of intestine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bowel dysfunction", "shortest_name_length": 17}
{"curie": "UMLS:C1710042", "names": ["Secondary Osteosarcoma", "Secondary Bone Osteosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary Osteosarcoma", "shortest_name_length": 22}
{"curie": "MONDO:0017837", "names": ["multiple sclerosis-ichthyosis-factor VIII deficiency syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple sclerosis-ichthyosis-factor VIII deficiency syndrome", "shortest_name_length": 61}
{"curie": "MONDO:0100364", "names": ["genital herpes simplex type 1 infectious disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genital herpes simplex type 1 infectious disorder", "shortest_name_length": 49}
{"curie": "UMLS:C3899644", "names": ["Protoplasmic Astrocytoma", "childhood protoplasmic astrocytoma", "Childhood Protoplasmic Astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Protoplasmic Astrocytoma", "shortest_name_length": 24}
{"curie": "UMLS:C0024799", "names": ["Stomal Ulcer", "Stomal ulcer", "stomal ulcer", "ULCER, STOMAL", "Ulcer, stomal", "marginal ulcer", "Marginal ulcer", "Marginal Ulcer", "Ulcer;marginal", "Marginal Ulcers", "ULCER, MARGINAL", "Ulcer, Marginal", "Ulcers, Marginal", "Anastomotic ulcer", "ANASTOMOTIC ULCER", "ULCER, ANASTOMOTIC", "Gastrojejunal ulcer", "ULCER GASTROJENUNAL", "gastrojejunal ulcer", "Ulcer;gastrojejunal", "Gastrojejunal Ulcer", "Ulcer gastrojejunal", "gastro jejunal ulcer", "gastrojejunal; ulcer", "ulcer; gastrojejunal", "Gastro-jejunal ulcer", "Anastomotic ulcer, NOS", "Gastrojejunal ulcer, NOS", "GJU - Gastrojejunal ulcer", "intestinal; ulcer, marginal", "Gastrojejunal ulcer (disorder)", "gastrojejunal ulcer (diagnosis)", "ulcer; bowel, intestine, marginal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Marginal ulcer", "shortest_name_length": 12}
{"curie": "MONDO:0007495", "names": ["DRD", "DYT5a", "DYT-GCH1", "dystonia 5", "dystonia type 5", "GTPCH1-deficient DRD", "dystonia, DOPA-responsive", "autosomal dominant Segawa syndrome", "HPD with marked diurnal fluctuation", "Segawa syndrome, autosomal dominant", "GTPCH1-deficient dopa-responsive dystonia", "autosomal dominant dopa-responsive dystonia", "Dopa-responsive dystonia, autosomal dominant", "Dopa-responsive dystonia; Segawa syndrome AD", "dystonia, progressive, with diurnal variation", "dystonia, Dopa-responsive, autosomal dominant", "dystonia-Parkinsonism with diurnal fluctuation", "GTP cyclohydrolase 1-deficient dopa-responsive dystonia", "hereditary progressive dystonia with marked diurnal fluctuation", "dystonia, DOPA-responsive, with or without hyperphenylalaninemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dystonia 5", "shortest_name_length": 3}
{"curie": "MONDO:0003062", "names": ["Benign Intestine Tumor", "benign intestine tumor", "benign intestinal tumor", "Benign Intestinal Tumor", "benign intestinal tumors", "Benign Intestinal Tumors", "intestinal tumors, benign", "Intestinal Tumors, Benign", "Benign tumor of intestine", "intestine benign neoplasm", "Benign Intestine Neoplasm", "benign intestine neoplasm", "intestinal benign neoplasm", "Benign Intestinal Neoplasm", "benign intestinal neoplasm", "Benign Tumor of Intestines", "Benign tumour of intestine", "benign tumor of intestines", "Benign Intestinal Neoplasms", "benign intestinal neoplasms", "intestinal neoplasms, benign", "Benign neoplasm of intestine", "Intestinal Neoplasms, Benign", "Benign Neoplasm of Intestines", "benign neoplasm of intestines", "benign tumor of the intestines", "Benign Tumor of the Intestines", "Benign neoplasm of intestine NOS", "Benign Neoplasm of the Intestines", "benign neoplasm of the intestines", "Benign neoplasm of intestinal tract", "Benign neoplasm of intestinal tract NOS", "Benign neoplasm of intestinal tract, NOS", "Benign neoplasm of intestinal tract (disorder)", "benign neoplasms of large and/or small intestine", "Benign Neoplasms of Large and/or Small Intestine", "benign neoplasms of the large and/or small intestine", "Benign Neoplasms of the Large and/or Small Intestine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intestinal benign neoplasm", "shortest_name_length": 22}
{"curie": "MONDO:0006880", "names": ["oral leukoedema", "Oral Leukoedema", "Oral leukoedema", "Oral Leukoedemas", "Leukoedema, Oral", "Leukoedemas, Oral", "leukedema of mouth", "Leukedema of mouth", "Leukoedema of mouth", "leukoedema of mouth", "Leukedema of mouth (disorder)", "leukoedema of mouth (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oral leukoedema", "shortest_name_length": 15}
{"curie": "MONDO:0005177", "names": ["Serous Cystoma", "Serous cystoma", "serous cystoma", "CYSTADENOMA SEROUS", "Serous cystadenoma", "cystadenoma serous", "serous cystadenoma", "Serous Cystadenoma", "Cystadenoma, Serous", "Serous Cystadenomas", "Cystadenomas, Serous", "Serous cystadenoma NOS", "Serous cystadenoma, NOS", "Serous microcystic adenoma", "serous; cystoma, unspecified site", "cystoma; serous, unspecified site", "Serous cystadenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "serous cystadenoma", "shortest_name_length": 14}
{"curie": "UMLS:C1332943", "names": ["Anaplastic Oligodendroglioma", "Anaplastic Childhood Oligodendroglioma", "anaplastic pediatric oligodendroglioma", "Anaplastic Pediatric Oligodendroglioma", "anaplastic childhood oligodendroglioma", "Childhood Anaplastic Oligodendroglioma", "childhood anaplastic oligodendroglioma", "undifferentiated pediatric oligodendroglioma", "undifferentiated childhood oligodendroglioma", "Undifferentiated Childhood Oligodendroglioma", "Undifferentiated Pediatric Oligodendroglioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Anaplastic Oligodendroglioma", "shortest_name_length": 28}
{"curie": "MONDO:0010375", "names": ["DEE8", "EIEE8", "HYPEREKPLEXIA AND EPILEPSY", "Hyperekplexia and Epilepsy", "hyperekplexia and epilepsy", "hyperekplexia-epilepsy syndrome", "early infantile epileptic encephalopathy 8", "developmental and epileptic encephalopathy 8", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 8", "epileptic encephalopathy, early infantile, 8", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 8", "developmental and epileptic encephalopathy, 8", "epileptic encephalopathy, early infantile, type 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 8", "shortest_name_length": 4}
{"curie": "MONDO:0003620", "names": ["PNS disease", "PNS Disease", "PNS disorder", "PNS diseases", "PNS Diseases", "Peripheral Neuropathy", "NEUROPATHY PERIPHERAL", "Neuropathy peripheral", "Peripheral neuropathy", "peripheral neuropathy", "PERIPHERAL NEUROPATHY", "neuropathy; peripheral", "Neuropathy, Peripheral", "neuropathy, peripheral", "peripheral neuropathies", "peripheral Neuropathies", "Peripheral neuropathies", "peripheral; neuropathic", "Peripheral Neuropathies", "Peripheral nerve disease", "Peripheral Nerve Disease", "peripheral nerve disease", "Peripheral Nerve Diseases", "peripheral nerve disorder", "peripheral nerve diseases", "nerve disease, peripheral", "Peripheral neuropathy NOS", "Nerve Disease, Peripheral", "Peripheral neuropathy, NOS", "PERIPHERAL NERVE DISORDERS", "Peripheral Nerve Disorders", "nerve diseases, peripheral", "peripheral nerve disorders", "Nerve Diseases, Peripheral", "Nerves, Peripheral--Diseases", "Peripheral nerve disorder NOS", "Peripheral nerve disorder, NOS", "peripheral nervous system disease", "Peripheral Nervous System Disease", "Peripheral nervous system disease", "peripheral nervous system disorder", "Peripheral Nervous System Disorder", "Peripheral Nervous System Diseases", "peripheral nervous system disorders", "Peripheral nerve disease (disorder)", "Peripheral Nervous System Disorders", "peripheral nerve disease (diagnosis)", "peripheral; nervous system, disorder", "disease of peripheral nervous system", "disorder of peripheral nervous system", "Disorder of Peripheral Nervous System", "disorders of peripheral nervous system", "PNS (Peripheral Nervous System) Diseases", "PNS (peripheral nervous system) diseases", "Disorder of peripheral nervous system NOS", "disorder of the peripheral nervous system", "Disorder of the peripheral nervous system", "DISORDERS OF THE PERIPHERAL NERVOUS SYSTEM", "Disorders of the peripheral nervous system", "Abnormal peripheral nervous system structure", "Abnormal peripheral nervous system morphology", "Peripheral nervous system disease or syndrome", "peripheral nervous system disease or disorder", "Disorder of the peripheral nervous system, NOS", "Peripheral Nervous System Diseases and Syndromes", "Non-Neoplastic Peripheral Nervous System Disease", "disease or disorder of peripheral nervous system", "Non-Neoplastic Peripheral Nervous System Disorder", "disorders of peripheral nervous system (diagnosis)", "Disorder of the peripheral nervous system (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peripheral nervous system disorder", "shortest_name_length": 11}
{"curie": "UMLS:C4744698", "names": ["Thyroid Gland Mucinous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid Gland Mucinous Carcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C1336053", "names": ["SCL/PL", "Spindle Cell/Pleomorphic Lipoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spindle Cell/Pleomorphic Lipoma", "shortest_name_length": 6}
{"curie": "UMLS:C0392034", "names": ["gastroesophagitis", "Gastroesophagitis", "Gastrooesophagitis", "Gastro-oesophagitis", "Gastroesophagitis, NOS", "Gastroesophagitis (disorder)", "gastroesophagitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastroesophagitis", "shortest_name_length": 17}
{"curie": "MONDO:0000104", "names": ["Microcytic anemia with liver iron overload", "Microcytic anaemia with liver iron overload", "Microcytic anemia and hepatic iron overload", "Microcytic anaemia and hepatic iron overload", "Hypochromic microcytic anemia with iron overload", "Hypochromic microcytic anaemia with iron overload", "anemia, hypochromic microcytic with iron overload", "Anemia, Hypochromic Microcytic, With Iron Overload", "ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD", "anemia, hypochromic microcytic, with iron overload", "Hypochromic microcytic anemia with iron overload (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anemia, hypochromic microcytic with iron overload", "shortest_name_length": 42}
{"curie": "MONDO:0004559", "names": ["glandular MPNST", "Glandular MPNST", "Malignant Glandular Schwannoma", "malignant glandular schwannoma", "Glandular Malignant Peripheral Nerve Sheath Tumor", "Glandular malignant peripheral nerve sheath tumor", "glandular malignant peripheral nerve sheath tumor", "malignant glandular peripheral nerve sheath tumor", "Malignant Glandular Peripheral Nerve Sheath Tumor", "Glandular malignant peripheral nerve sheath tumour", "malignant glandular peripheral nerve sheath neoplasm", "Malignant Glandular Peripheral Nerve Sheath Neoplasm", "malignant glandular tumor of peripheral nerve sheath", "Malignant Glandular Tumor of Peripheral Nerve Sheath", "Malignant Glandular Neoplasm of Peripheral Nerve Sheath", "malignant glandular neoplasm of peripheral nerve sheath", "malignant glandular tumor of the peripheral nerve sheath", "Malignant Glandular Tumor of the Peripheral Nerve Sheath", "Malignant Glandular Neoplasm of the Peripheral Nerve Sheath", "malignant glandular neoplasm of the peripheral nerve sheath", "Glandular malignant peripheral nerve sheath tumor (disorder)", "Glandular malignant peripheral nerve sheath tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant glandular tumor of peripheral nerve sheath", "shortest_name_length": 15}
{"curie": "MONDO:0003355", "names": ["ovary leiomyosarcoma", "ovarian leiomyosarcoma", "Ovarian Leiomyosarcoma", "Leiomyosarcoma of Ovary", "leiomyosarcoma of Ovary", "leiomyosarcoma of ovary", "Leiomyosarcoma of the Ovary", "leiomyosarcoma of the ovary", "leiomyosarcoma of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovary leiomyosarcoma", "shortest_name_length": 20}
{"curie": "UMLS:C2981377", "names": ["Stage IIIC Esophageal Squamous Cell Cancer", "Stage IIIC Esophageal Squamous Cell Carcinoma", "Stage IIIC Esophageal Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Esophageal Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 42}
{"curie": "UMLS:C1333845", "names": ["Grade 3 Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade 3 Malignant Neoplasm", "shortest_name_length": 26}
{"curie": "UMLS:C1333938", "names": ["Hard Palate Mucoepidermoid Carcinoma", "Mucoepidermoid Carcinoma of Hard Palate", "Mucoepidermoid Carcinoma of the Hard Palate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hard Palate Mucoepidermoid Carcinoma", "shortest_name_length": 36}
{"curie": "MONDO:0003879", "names": ["Endometrioid adenofibroma, malignant", "Ovarian Endometrioid Adenocarcinofibroma", "ovarian endometrioid adenocarcinofibroma", "ovarian endometrioid malignant adenofibroma", "Ovarian Endometrioid Malignant Adenofibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian endometrioid adenocarcinofibroma", "shortest_name_length": 36}
{"curie": "MONDO:0007517", "names": ["Ecp syndrome", "ECP SYNDROME", "ECTRODACTYLY-CLEFT PALATE SYNDROME", "Ectrodactyly-Cleft Palate Syndrome", "ectrodactyly-cleft palate syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectrodactyly-cleft palate syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0015064", "names": ["jejunal neuroendocrine tumor", "Jejunal Neuroendocrine Tumor", "jejunal neuroendocrine neoplasm", "jejunal neuroendocrine tumor, well differentiated, low or intermediate grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "jejunal neuroendocrine tumor, well differentiated, low or intermediate grade", "shortest_name_length": 28}
{"curie": "MONDO:0010070", "names": ["BCYM1A", "Brachyolmia Type 1, Hobaek Type", "brachyolmia type 1, Hobaek type", "BRACHYOLMIA TYPE 1, HOBAEK TYPE", "Brachyolmia type 1, Hobaek type", "Brachyolmia, recessive Hobaek type", "brachyolmia, recessive type of Hobaek", "Brachyolmia, Recessive Type Of Hobaek", "BRACHYOLMIA, RECESSIVE TYPE OF HOBAEK", "SPONDYLODYSPLASIA WITH PURE BRACHYOLMIA", "Spondylodysplasia with pure brachyolmia", "spondylodysplasia with Pure brachyolmia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachyolmia type 1, Hobaek type", "shortest_name_length": 6}
{"curie": "UMLS:C0159333", "names": ["MANDIBLE FRACTURE MULTIPLE CLOSED", "Multiple sites of mandible closed fracture", "Closed fracture of mandible, multiple sites", "Closed Fracture of Mandible, Multiple Sites", "closed fracture of multiple sites of mandible", "Closed fracture of multiple sites of mandible", "Closed fracture of multiple sites of mandible (disorder)", "closed fracture of multiple sites of mandible (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Closed fracture of mandible, multiple sites", "shortest_name_length": 33}
{"curie": "UMLS:C1306063", "names": ["acute lv failure", "LEFT VENTRICULAR FAILURE ACUTE", "acute left ventricular failure", "Acute left ventricular failure", "Acute edema of lung with heart disease", "Acute oedema of lung with heart disease", "Acute pulmonary edema with heart disease", "Acute left ventricular failure (disorder)", "Acute pulmonary oedema with heart disease", "heart; disease, with acute pulmonary edema", "acute left ventricular failure (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute left ventricular failure", "shortest_name_length": 16}
{"curie": "UMLS:C0855149", "names": ["Stage I B-Lymphoblastic Lymphoma", "Stage I B Lymphoblastic Lymphoma", "Stage I Precursor B-Lymphoblastic Lymphoma", "Precursor B-lymphoblastic lymphoma stage I", "Ann Arbor Stage I B Lymphoblastic Lymphoma", "Precursor B-Lymphoblastic Lymphoma Stage I", "Precursor B-lymphoblastic lymphoma NOS stage I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Precursor B-lymphoblastic lymphoma stage I", "shortest_name_length": 32}
{"curie": "MONDO:0014077", "names": ["LIS5", "lissencephaly 5", "LISSENCEPHALY 5", "lissencephaly type 5", "lissencephaly type 2 without muscular or eye involvement", "lissencephaly type 2 without muscular or ocular involvement", "cobblestone lissencephaly without muscular or eye involvement", "cobblestone lissencephaly without muscular or ocular involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cobblestone lissencephaly without muscular or ocular involvement", "shortest_name_length": 4}
{"curie": "MONDO:0022428", "names": ["Shaver", "aluminosis", "Aluminosis", "Bauxite lung", "aluminum lung", "Aluminum lung", "Aluminium lung", "aluminium lung", "Shavers disease", "shavers disease", "aluminium lungs", "Shaver's disease", "Bauxite fibrosis", "shavers' disease", "Shavers' disease", "fibrosis; bauxite", "bauxite; fibrosis", "Aluminosis of lung", "aluminosis of lung", "Aluminosis pulmonum", "pulmonary aluminosis", "Aluminosis (of lung)", "bauxite pneumoconiosis", "Bauxite pneumoconiosis", "bauxite; pneumoconiosis", "aluminum pneumoconiosis", "Corundum smelters' lung", "Aluminum pneumoconiosis", "pneumoconiosis; bauxite", "Bauxite workers' disease", "Bauxite fibrosis of lung", "pneumoconiosis; aluminum", "aluminum; pneumoconiosis", "Aluminium pneumoconiosis", "pneumoconiosis; aluminium", "aluminium; pneumoconiosis", "aluminum lung (diagnosis)", "Bauxite fibrosis (of lung)", "Bauxite pulmonary fibrosis", "Bauxite fume pneumoconiosis", "Aluminosis of lung (disorder)", "pneumoconiosis due to bauxite", "fibrosis; lung, bauxite-induced", "lung; fibrosis, bauxite-induced", "Bauxite fibrosis of lung (disorder)", "pneumoconiosis due to bauxite (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aluminosis", "shortest_name_length": 6}
{"curie": "UMLS:C0234249", "names": ["Stump Neuralgia", "Stump neuralgia", "Neuralgia, stump", "Stump Neuralgias", "Neuralgia, Stump", "Neuralgias, Stump", "Neuralgia of amputation stump", "Neuralgia of amputation stump (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neuralgia, Stump", "shortest_name_length": 15}
{"curie": "MONDO:0008512", "names": ["Sd1", "SD1", "SDTY1", "Zygodactyly", "ZYGODACTYLY", "syndactyly type 1", "Syndactyly type 1", "SYNDACTYLY, TYPE I", "syndactyly, type 1", "Syndactyly, Type I", "Syndactyly type 1 (disorder)", "syndactyly type 1 (diagnosis)", "craniosynostosis, Philadelphia type", "chromosome 2q35 DUPLICATION syndrome", "CHROMOSOME 2q35 DUPLICATION SYNDROME", "chromosome 2q35 duplication syndrome", "syndactyly, type 1, with or without craniosynostosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndactyly type 1", "shortest_name_length": 3}
{"curie": "UMLS:C2717884", "names": ["Autoimmune Lymphoproliferative Syndrome Type 1, Autosomal Dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Autoimmune Lymphoproliferative Syndrome Type 1, Autosomal Dominant", "shortest_name_length": 66}
{"curie": "MONDO:0017086", "names": ["Tethered cord", "Spinal cord syndrome", "cord syndrome tethered", "tethered cord syndrome", "Tethered cord syndrome", "Tethered Cord Syndrome", "Tethered Cord Syndromes", "Occult Spinal Dysraphism", "Occult spinal dysraphism", "occult spinal dysraphism", "Occult Spinal Dysraphisms", "Spinal Dysraphism, Occult", "Dysraphism, Occult Spinal", "Spinal Dysraphisms, Occult", "Dysraphisms, Occult Spinal", "Tethered Spinal Cord Syndrome", "segmental vertebral anomalies", "primary tethered cord syndrome", "occult spinal dysraphism sequence", "Occult Spinal Dysraphism Sequence", "Occult spinal dysraphism sequence", "tethered cord syndrome (diagnosis)", "Congenital tethering of spinal cord", "Tethered cord malformation sequence", "primary tethered spinal cord syndrome", "Occult spinal dysraphism sequence (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary tethered cord syndrome", "shortest_name_length": 13}
{"curie": "MONDO:0003908", "names": ["clivus meningioma", "Clivus Meningioma", "meningioma (clivus)", "Meningioma of Clivus", "meningioma of clivus", "Meningioma of the Clivus", "meningioma of the Clivus", "meningioma of the clivus", "meningioma of clivus (diagnosis)", "clivus of occipital bone meningioma (disease)", "meningioma (disease) of clivus of occipital bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "clivus meningioma", "shortest_name_length": 17}
{"curie": "UMLS:C1560249", "names": ["CARDIAC ARRHYTHMIA", "Adverse Event Associated with Cardiac Arrhythmia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adverse Event Associated with Cardiac Arrhythmia", "shortest_name_length": 18}
{"curie": "MONDO:0009814", "names": ["Osteopenia and sparse hair", "OSTEOPENIA AND SPARSE HAIR", "osteopenia and sparse hair", "Kaler-Garrity-Stern syndrome", "Kaler Garrity Stern syndrome", "Osteopenia mental retardation sparse hair", "osteopenia mental retardation sparse hair", "osteopenia intellectual disability sparse hair", "Osteopenia-intellectual disability-sparse hair syndrome", "osteopenia-intellectual disability-sparse hair syndrome", "osteopenia, intellectual disability, sparse hair syndrome", "Osteopenia, intellectual disability, sparse hair syndrome", "Osteopenia, intellectual disability, sparse hair syndrome (disorder)", "osteopenia, intellectual disability, sparse hair syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteopenia-intellectual disability-sparse hair syndrome", "shortest_name_length": 26}
{"curie": "MONDO:0017094", "names": ["Cortical dysplasia", "cortical dysplasia", "dysplasia cortical", "Cortical Dysplasia", "cortical dysplasias", "Dysplasia, Cortical", "Cortical Dysplasias", "Neocortical dysplasia", "Brain cortical dysplasia", "brain cortical dysplasia", "Cerebral Cortical Dysplasia", "cerebral cortical dysplasia", "Cerebral cortical dysplasia", "Dysplasia, Cerebral Cortical", "Cerebral Cortical Dysplasias", "Dysplasia of cerebral cortex", "Cortical Dysplasia, Cerebral", "Cortical dysplasia (disorder)", "Cortical dysplasia (diagnosis)", "Cortical Development Malformation", "Cortical Development Malformations", "Development Malformation, Cortical", "Malformations of Cortical Development", "Malformations of cortical development", "Dysplasia of cerebral cortex (diagnosis)", "disorder of brain cerebral cortex dysplasia", "Malformations of Cerebral Cortex Development", "congenital malformation brain cortical dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebral cortical dysplasia", "shortest_name_length": 18}
{"curie": "MONDO:0024527", "names": ["GFND1", "lobular glomerulopathy, familial", "glomerulopathy with fibronectin deposits 1", "glomerulopathy with giant fibrillar deposits"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glomerulopathy with fibronectin deposits 1", "shortest_name_length": 5}
{"curie": "MONDO:0004675", "names": ["Mitochondrial encephalomyopathy", "Mitochondrial myoencephalopathy", "mitochondrial encephalomyopathy", "Mitochondrial Encephalomyopathy", "ENCEPHALOMYOPATHY, MITOCHONDRIAL", "Encephalomyopathy, Mitochondrial", "encephalomyopathies mitochondrial", "Mitochondrial Encephalomyopathies", "Encephalomyopathies, Mitochondrial", "Mitochondrial encephalomyopathy (disorder)", "mitochondrial encephalomyopathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial encephalomyopathy", "shortest_name_length": 31}
{"curie": "MONDO:0003422", "names": ["lung adenoma", "adenoma lung", "Lung Adenoma", "adenoma lungs", "Adenoma of lung", "adenoma of lung", "Adenoma of Lung", "pulmonary adenoma", "Pulmonary Adenoma", "Adenoma of the Lung", "adenoma of the lung", "Adenoma of lung (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung adenoma", "shortest_name_length": 12}
{"curie": "UMLS:C1332526", "names": ["Benign Ovarian Partly Luteinized Thecoma", "Benign Partly Luteinized Thecoma of Ovary", "Ovarian Partly Luteinized Theca Cell Tumor", "Partly Luteinized Theca Cell Tumor of Ovary", "Benign Partly Luteinized Thecoma of the Ovary", "Ovarian Partly Luteinized Theca Cell Neoplasm", "Partly Luteinized Theca Cell Neoplasm of Ovary", "Partly Luteinized Theca Cell Tumor of the Ovary", "Partly Luteinized Theca Cell Neoplasm of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Ovarian Partly Luteinized Thecoma", "shortest_name_length": 40}
{"curie": "MONDO:0024227", "names": ["miliaria pustular", "Pustular miliaria", "Miliaria pustulosa", "miliaria pustulosa", "Miliaria pustulosa (disorder)", "miliaria pustulosa (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "miliaria pustulosa", "shortest_name_length": 17}
{"curie": "UMLS:C0020610", "names": ["HYPOGALACTIA", "Hypogalactia", "hypogalactia", "Hypolactation", "Hypogalactias", "Poor lactation", "Decreased lactation", "LACTATION DECREASED", "Lactation decreased", "Lactation, decreased", "lactation; defective", "Inadequate lactation", "defective; lactation", "Insufficient lactation", "hypogalactia (diagnosis)", "Milk production decreased", "Decreased lactation (finding)", "insufficiency; lactation, partial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypogalactia", "shortest_name_length": 12}
{"curie": "MONDO:0008051", "names": ["TAM1", "tubular aggregate myopathy", "tubular aggregate myopathy 1", "myopathy, tubular aggregate, 1", "myopathy, tubular aggregate, type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tubular aggregate myopathy", "shortest_name_length": 4}
{"curie": "MONDO:0014409", "names": ["MRT44", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 44", "mental retardation, autosomal recessive 44", "mental retardation, autosomal recessive type 44", "intellectual disability, autosomal recessive 44", "intellectual disability, autosomal recessive type 44", "autosomal recessive intellectual developmental disorder 44", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 44", "METTL23 autosomal recessive non-syndromic intellectual disability", "autosomal recessive non-syndromic intellectual disability caused by mutation in METTL23"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 44", "shortest_name_length": 5}
{"curie": "MONDO:0001274", "names": ["Anal spasm", "spasm anal", "anal spasm", "ANAL SPASM", "anus; spasm", "anal spasms", "proctospasm", "spasm; anus", "anal spasm (symptom)", "Anal spasm (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anal spasm", "shortest_name_length": 10}
{"curie": "MONDO:0030872", "names": ["FTDALS8", "FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 8", "frontotemporal dementia and/or amyotrophic lateral sclerosis 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontotemporal dementia and/or amyotrophic lateral sclerosis 8", "shortest_name_length": 7}
{"curie": "UMLS:C1318500", "names": ["Nontoxic nodular goiter", "nontoxic nodular goiter", "nodular nontoxic goiter", "Nontoxic nodular goitre", "Non-toxic nodular goiter", "non-toxic nodular goiter", "Non-toxic nodular goitre", "Non-Toxic Nodular Goiter", "nodular non toxic goiter", "non toxic nodular goiter", "GOITER, NODULAR, NONTOXIC", "Nontoxic nodular goiter NOS", "Nodular goiter (nontoxic) NOS", "Non-toxic nodular goiter, NOS", "Non-toxic nodular goitre, NOS", "Nontoxic nodular thyroid goitre", "Nontoxic nodular thyroid goiter", "Non-toxic nodular goiter (disorder)", "Unspecified nontoxic nodular goiter", "nontoxic nodular goiter (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-toxic nodular goiter", "shortest_name_length": 23}
{"curie": "UMLS:C1096119", "names": ["Cardiac valve replacement complication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cardiac valve replacement complication", "shortest_name_length": 38}
{"curie": "UMLS:C1511263", "names": ["Borderline Ovarian Mucinous Tumor", "Borderline Ovarian Mucinous Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Ovarian Mucinous Tumor", "shortest_name_length": 33}
{"curie": "UMLS:C1096262", "names": ["Escherichia bacteremia", "Escherichia bacteraemia", "Escherichia coli bacteremia", "Escherichia coli bacteraemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Escherichia bacteremia", "shortest_name_length": 22}
{"curie": "UMLS:C0428990", "names": ["Non-conducted SVE", "Premature Atrial Complex Blocked", "Blocked Atrial Premature Complex", "PREMATURE ATRIAL COMPLEXES BLOCKED", "atrial premature complex with block", "Blocked premature atrial contraction", "Premature Atrial Complexes Non-conducted", "Atrial premature complexes, nonconducted", "Blocked Atrial Premature Complex by ECG Finding", "Blocked premature atrial contraction (disorder)", "Blocked Atrial Premature Complex by EKG Finding", "atrial premature complex with block (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Blocked premature atrial contraction", "shortest_name_length": 17}
{"curie": "MONDO:0054722", "names": ["GPHYSD3", "GELEOPHYSIC dysplasia 3", "GELEOPHYSIC DYSPLASIA 3", "geleophysic dysplasia 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "geleophysic dysplasia 3", "shortest_name_length": 7}
{"curie": "MONDO:0012878", "names": ["CWS2", "Cowden syndrome 2", "SDHB Cowden disease", "Cowden-Like Syndrome", "Cowden syndrome type 2", "COWDEN-LIKE SYNDROME (disorder)", "Cowden disease caused by mutation in SDHB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cowden syndrome 2", "shortest_name_length": 4}
{"curie": "MONDO:0100445", "names": ["LCA5", "LCA5 retinopathy", "LCA5-related retinopathy", "Leber congenital amaurosis 5", "LCA5 Leber congenital amaurosis", "Leber congenital amaurosis type 5", "amaurosis congenita of Leber, type 5", "Leber congenital amaurosis caused by mutation in LCA5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "LCA5-related retinopathy", "shortest_name_length": 4}
{"curie": "MONDO:0032779", "names": ["NEDMIBA", "NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY AND STRUCTURAL BRAIN ANOMALIES", "neurodevelopmental disorder with microcephaly and structural brain anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with microcephaly and structural brain anomalies", "shortest_name_length": 7}
{"curie": "MONDO:0018292", "names": ["CDG-related bone disorder", "congenital disorder of glycosylation-related bone disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital disorder of glycosylation-related bone disorder", "shortest_name_length": 25}
{"curie": "UMLS:C4520987", "names": ["Carcinoma in situ of Antrum", "Carcinoma In Situ of the Antrum", "Gastric Antrum Carcinoma In Situ", "Gastric Antrum Carcinoma in situ", "Stage 0 Carcinoma of Gastric Antrum", "Stage 0 Carcinoma of the Gastric Antrum", "Gastric Antrum Carcinoma In Situ AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Antrum Carcinoma In Situ AJCC v6 and v7", "shortest_name_length": 27}
{"curie": "UMLS:C0332679", "names": ["Crushed", "Crush injury", "crush injury", "Injury;crush", "INJURY CRUSH", "Crush Injury", "Injury, Crush", "Crush Injuries", "crush injuries", "Injuries, Crush", "Crushing injury", "pressure injury", "CRUSHING INJURY", "Crushing Injury", "crushing injury", "Crush injury NOS", "CRUSHING INJURIES", "crushing injuries", "injuries pressure", "Crush injury, NOS", "Compression injury", "compression injury", "compression injuries", "Crushing injury, NOS", "Pressure injury, NOS", "COMPRESSION INJURIES", "Compression injury, NOS", "crush injury (diagnosis)", "Crushing injury - disorder", "Crushing injury (disorder)", "Crushing injury (morphology)", "Crushing injury of unspecified site", "Crushing injury (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Crushing injury", "shortest_name_length": 7}
{"curie": "UMLS:C0154045", "names": ["Benign neoplasm of aortic body and other paraganglia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign neoplasm of aortic body and other paraganglia", "shortest_name_length": 52}
{"curie": "MONDO:0012333", "names": ["DFNB53", "autosomal recessive deafness 53", "DEAFNESS, AUTOSOMAL RECESSIVE 53", "deafness, autosomal recessive 53", "Deafness, Autosomal Recessive 53", "deafness, autosomal recessive type 53", "autosomal recessive nonsyndromic deafness 53", "autosomal recessive nonsyndromic hearing loss 53", "autosomal recessive nonsyndromic deafness type 53", "COL11A2 autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic deafness caused by mutation in COL11A2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 53", "shortest_name_length": 6}
{"curie": "MONDO:0007982", "names": ["MCDJ", "Jansen disease", "Jansen Disease", "Jansen Metaphyseal Dysostosis", "Jansen metaphyseal dysostosis", "Metaphyseal dysostosis, Jansen type", "Jansen metaphyseal chondrodysplasia", "Jansen's metaphyseal chondrodysplasia", "Jansen type metaphyseal chondrodysplasia", "Metaphyseal Chondrodysplasia, Jansen Type", "METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE", "metaphyseal chondrodysplasia, Jansen type", "Metaphyseal chondrodysplasia, Jansen type", "Murk Jansen Type Metaphyseal Chondrodysplasia", "Murk Jansen type metaphyseal chondrodysplasia", "metaphyseal chondrodysplasia murk Jansen type", "murk Jansen type metaphyseal chondrodysplasia", "Metaphyseal chondrodysplasia Murk Jansen type", "METAPHYSEAL CHONDRODYSPLASIA, MURK JANSEN TYPE", "Jansen's metaphyseal chondrodysplasia syndrome", "metaphyseal chondrodysplasia, murk Jansen type", "Metaphyseal Chondrodysplasia, Murk Jansen Type", "Metaphyseal chondrodysplasia, Jansen type (disorder)", "Metaphyseal chondrodysplasia, Jansen type (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metaphyseal chondrodysplasia, Jansen type", "shortest_name_length": 4}
{"curie": "MONDO:0001300", "names": ["Autonomic neuropathy", "NEUROPATHY AUTONOMIC", "autonomic neuropathy", "AUTONOMIC NEUROPATHY", "Autonomic Neuropathy", "neuropathy autonomic", "autonomic neuropathies", "Autonomic neuropathy NOS", "Autonomic neuropathy (disorder)", "autonomic peripheral neuropathy", "autonomic nervous system peripheral neuropathy", "peripheral neuropathy of autonomic nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autonomic neuropathy", "shortest_name_length": 20}
{"curie": "MONDO:0019235", "names": ["disorder of phenylalanin or tyrosine metabolism", "inborn disorder of phenylalanin or tyrosine metabolism", "inborn disorder of phenylalanine and tyrosine metabolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of phenylalanine and tyrosine metabolism", "shortest_name_length": 47}
{"curie": "UMLS:C1335023", "names": ["Non-Neoplastic Neck Disease", "Non-Neoplastic Neck Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Neck Disorder", "shortest_name_length": 27}
{"curie": "UMLS:C1335362", "names": ["Parotid monomorphic adenoma", "Parotid Monomorphic Adenoma", "Monomorphic Adenoma of Parotid", "Parotid Gland Monomorphic Adenoma", "Monomorphic Adenoma of the Parotid", "Monomorphic Adenoma of Parotid Gland", "Monomorphic Adenoma of the Parotid Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parotid monomorphic adenoma", "shortest_name_length": 27}
{"curie": "MONDO:0008803", "names": ["ABS2", "antley-bixler syndrome", "Antley Bixler Syndrome", "antley bixler syndrome", "Antley Bixler syndrome", "Antley-Bixler Syndrome", "Antley-Bixler syndrome", "Syndrome, Antley-Bixler", "Antley and Bixler's syndrome", "Antley-Bixler Syndrome Type 2", "Antley Bixler Syndrome Type 2", "Multisynostotic Osteodysgenesis", "Multisynostotic osteodysgenesis", "Osteodysgenesis, Multisynostotic", "Antley-Bixler syndrome (disorder)", "Trapezoidcephaly-multiple synostosis", "trapezoidocephaly synostosis syndrome", "Trapezoidocephaly Synostosis Syndrome", "trapezoidocephaly-synostosis syndrome", "TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME", "Trapezoidocephaly-Synostosis Syndrome", "Syndrome, Trapezoidocephaly-Synostosis", "Trapezoidocephaly-Synostosis Syndromes", "Antley Bixler Syndrome, Autosomal Dominant", "Antley-Bixler Syndrome, Autosomal Dominant", "osteodysgenesis, multisynostotic with fractures", "osteodysgenesis, multisynostotic, with fractures", "Osteodysgenesis, Multisynostotic, With Fractures", "OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES", "Antley-Bixler syndrome with disordered steroidogenesis", "Multisynostotic Osteodysgenesis With Long Bone Fractures", "multisynostotic osteodysgenesis with long bone fractures", "MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES", "Antley-Bixler syndrome without genital anomaly or disorder of steroidogenesis", "ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Antley-Bixler syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0161802", "names": ["bone marrow transplant complications", "bone marrow transplant; complications", "Transplanted Bone Marrow Complication", "Complications of bone marrow transplant", "Complications of transplanted bone marrow", "bone marrow transplant complications (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Complications of bone marrow transplant", "shortest_name_length": 36}
{"curie": "UMLS:C5420068", "names": ["Unresectable Anal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Anal Squamous Cell Carcinoma", "shortest_name_length": 41}
{"curie": "UMLS:C4733552", "names": ["recurrent cutaneous squamous cell carcinoma of the head and neck", "Recurrent Cutaneous Squamous Cell Carcinoma of the Head and Neck"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Cutaneous Squamous Cell Carcinoma of the Head and Neck", "shortest_name_length": 64}
{"curie": "MONDO:0010432", "names": ["THPH8", "DEEP VENOUS THROMBOSIS, PROTECTION AGAINST", "deep Venous thrombosis, protection against", "X-linked thrombophilia due to factor IX defect", "thrombophilia, X-linked, due to factor 9 defect", "THROMBOPHILIA, X-LINKED, DUE TO FACTOR IX DEFECT", "Thrombophilia, X-Linked, Due To Factor Ix Defect", "thrombophilia, X-linked, due to factor IX defect", "deep venous thrombosis, protection against, X-linked recessive", "thrombophilia 8, X-linked, due to factor IX defect, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombophilia, X-linked, due to factor 9 defect", "shortest_name_length": 5}
{"curie": "UMLS:C5555949", "names": ["Uterine Ligament Leiomyoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Ligament Leiomyoma", "shortest_name_length": 26}
{"curie": "UMLS:C1696700", "names": ["C1 esterase deficiency acquired"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "C1 esterase deficiency acquired", "shortest_name_length": 31}
{"curie": "MONDO:0019239", "names": ["disorder of serine or glycine metabolism", "inborn disorder of serine family metabolism", "inborn disorder of serine or glycine metabolism", "inborn serine family amino acid metabolic process disorder", "inborn error of serine family amino acid metabolic process", "rare inborn error of serine family amino acid metabolic process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of serine family metabolism", "shortest_name_length": 40}
{"curie": "EFO:1001791", "names": ["femoral hernia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "femoral hernia", "shortest_name_length": 14}
{"curie": "MONDO:0006107", "names": ["THYROID TUMOR BENIGN", "benign thyroid tumor", "Benign Thyroid Tumor", "Benign Thyroid Neoplasm", "Benign Tumor of Thyroid", "benign thyroid neoplasm", "benign tumor of thyroid", "Benign neoplasm thyroid", "thyroid neoplasm, benign", "Thyroid Neoplasm, Benign", "Thyroid neoplasms benign", "Benign Neoplasm of Thyroid", "benign thyroid gland tumor", "Benign Thyroid Gland Tumor", "benign neoplasm of thyroid", "benign tumor of the thyroid", "Benign Thyroid Neoplasm NOS", "Benign thyroid neoplasm NOS", "Benign Tumor of the Thyroid", "Benign Tumor of Thyroid Gland", "thyroid gland benign neoplasm", "benign thyroid gland neoplasm", "Benign tumor of thyroid gland", "Neoplasm benign;thyroid gland", "Benign Thyroid Gland Neoplasm", "benign tumor of thyroid gland", "Benign Neoplasm of the Thyroid", "benign neoplasm of the thyroid", "Benign tumour of thyroid gland", "Benign neoplasm of the thyroid", "Benign Neoplasm of Thyroid Gland", "Benign neoplasm of thyroid gland", "benign neoplasm of thyroid gland", "Benign Tumor of the Thyroid Gland", "benign tumor of the thyroid gland", "Benign neoplasm of thyroid glands", "benign neoplasm of thyroid glands", "Benign Neoplasm of Thyroid Glands", "benign neoplasm of the thyroid gland", "Benign Neoplasm of the Thyroid Gland", "Benign neoplasm of thyroid gland (disorder)", "benign neoplasm of thyroid gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign thyroid gland neoplasm", "shortest_name_length": 20}
{"curie": "MONDO:0018279", "names": ["CMD-no MR", "CMD without intellectual disability", "congenital muscular dystrophy without intellectual disability", "congenital muscular dystrophy-dystroglycanopathy without intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital muscular dystrophy without intellectual disability", "shortest_name_length": 9}
{"curie": "UMLS:C0342302", "names": ["labile diabetes", "Labile diabetes", "brittle diabetes", "Brittle diabetes", "Diabetes brittle", "diabetes; brittle", "brittle; diabetes", "unstable; diabetes", "diabetes; unstable", "brittle diabetes mellitus", "Brittle diabetes mellitus", "Brittle Diabetes Mellitus", "Diabetes mellitus, labile", "Unstable diabetes mellitus", "Diabetes Mellitus, Brittle", "Diabetes mellitus, brittle", "Brittle diabetes mellitus (finding)", "brittle diabetes mellitus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brittle diabetes", "shortest_name_length": 15}
{"curie": "UMLS:C2981394", "names": ["Stage I Appendix Carcinoid Tumor", "Stage I Appendix Neuroendocrine Tumor", "Stage I Appendix Carcinoid Tumor AJCC v7", "Stage I Appendix Neuroendocrine Tumor AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Appendix Neuroendocrine Tumor AJCC v7", "shortest_name_length": 32}
{"curie": "MONDO:0700035", "names": ["del(8)", "Loss of Chromosome 8", "loss of chromosome 8", "Chromosome 8 deletion", "Chromosome 8 Deletion", "monosomy chromosome 8", "chromosome 8 deletion", "Deletions of chromosome 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "monosomy chromosome 8", "shortest_name_length": 6}
{"curie": "MONDO:0010635", "names": ["HH1", "KMS", "KAL1", "Kallmann syndrome 1", "KALLMANN SYNDROME 1", "Kallmann Syndrome 1", "anosmic hypogonadism", "Kallmann syndrome, X-linked", "ANOS1 hypogonadotropic hypogonadism", "Kallmann syndrome, type 1, X-linked", "Kallmann Syndrome, Type 1, X-linked", "dysplasia olfactogenitalis of de Morsier", "dysplasia Olfactogenitalis of De Morsier", "dysplasia olfactogenitalis of de morsier", "hypogonadotropic hypogonadism and anosmia", "hypogonadotropic hypogonadism 1 with or without anosmia", "HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA", "hypogonadotropic hypogonadism caused by mutation in ANOS1", "hypogonadotropic hypogonadism 1 with or without anosmia (Kallmann syndrome 1), X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadotropic hypogonadism 1 with or without anosmia", "shortest_name_length": 3}
{"curie": "MONDO:0020502", "names": ["YF", "Bronze John", "bronze John", "Yellow Jack", "Yellow Fever", "Yellow fever", "YELLOW FEVER", "yellow fever", "febris; flava", "Fever, Yellow", "flava; febris", "Yellow Fevers", "Fevers, Yellow", "YF - Yellow fever", "Yellow fever, NOS", "Urban yellow fever", "urban yellow fever", "Yellow fever, urban", "jungle yellow fever", "urban; yellow fever", "yellow fever; urban", "Sylvan yellow fever", "Jungle yellow fever", "Yellow fever, sylvan", "Yellow fever, jungle", "Sylvatic yellow fever", "sylvatic yellow fever", "yellow fever; sylvatic", "sylvatic; yellow fever", "Yellow fever (disorder)", "yellow fever (diagnosis)", "Unspecified yellow fever", "Yellow fever, unspecified", "fever; jungle, yellow fever", "fever; jungle fever, yellow", "jungle; fever, yellow fever", "Yellow fever Virus infection", "Yellow Fever Virus Infection", "Yellow fever virus infection", "Urban yellow fever (disorder)", "urban yellow fever (diagnosis)", "Jungle yellow fever (disorder)", "jungle yellow fever; yellow fever", "yellow fever; jungle yellow fever", "sylvatic yellow fever (diagnosis)", "Yellow fever virus infectious disease", "Yellow fever virus disease or disorder", "Yellow fever virus caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "yellow fever", "shortest_name_length": 2}
{"curie": "MONDO:0011829", "names": ["COQ10D1", "CoQ DEFICIENCY 1", "CoQ deficiency 1", "ubiquinone deficiency 1", "COENZYME Q DEFICIENCY 1", "coenzyme Q deficiency 1", "UBIQUINONE DEFICIENCY 1", "CoQ10 deficiency, primary, 1", "COQ2 coenzyme Q10 deficiency", "Coq10 deficiency, primary, 1", "CoQ10 DEFICIENCY, PRIMARY, 1", "primary coenzyme Q10 deficiency 1", "COENZYME Q10 DEFICIENCY, PRIMARY, 1", "coenzyme Q10 deficiency, primary, 1", "coenzyme Q10 deficiency, primary, type 1", "coenzyme Q10 deficiency caused by mutation in COQ2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coenzyme Q10 deficiency, primary, 1", "shortest_name_length": 7}
{"curie": "UMLS:C5419806", "names": ["Neutrophil-Rich Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neutrophil-Rich Hepatocellular Carcinoma", "shortest_name_length": 40}
{"curie": "UMLS:C0280117", "names": ["stage IV adult NHL", "NHL, stage IV adult", "NHL, metastatic adult", "Stage IV Non-Hodgkin Lymphoma", "Stage IV Adult Non-Hodgkin Lymphoma", "stage IV adult non-Hodgkin lymphoma", "Stage IV Adult Non-Hodgkin's Lymphoma", "Adult Non-Hodgkin's Lymphoma Stage IV", "adult non-Hodgkin's lymphoma, stage IV", "non-Hodgkin's lymphoma, stage IV adult", "lymphoma, stage IV, adult non-Hodgkin's", "metastatic adult non-Hodgkin's lymphoma", "adult non-Hodgkin's lymphoma, metastatic", "non-Hodgkin's lymphoma, metastatic adult", "lymphoma, metastatic, adult non-Hodgkin's", "Ann Arbor Stage IV Adult Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Adult Non-Hodgkin Lymphoma", "shortest_name_length": 18}
{"curie": "UMLS:C1518005", "names": ["Low-Grade CIN", "Low-Grade Cervical SIL", "Mild Squamous Dysplasia of the Cervix", "Cervical Squamous Intraepithelial Neoplasia 1", "Cervical low grade squamous intraepithelial lesion", "Low Grade Cervical Squamous Intraepithelial Lesion", "Low-Grade Cervical Squamous Intraepithelial Lesion", "Low Grade Cervical Squamous Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Grade Cervical Squamous Intraepithelial Neoplasia", "shortest_name_length": 13}
{"curie": "MONDO:0032564", "names": ["HKLLS3", "hennekam lymphangiectasia-lymphedema syndrome 3", "HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hennekam lymphangiectasia-lymphedema syndrome 3", "shortest_name_length": 6}
{"curie": "UMLS:C3639955", "names": ["Dextrocardia Normal Situs", "Dextrocardia, Normal Situs", "Dextrocardia Situs Solitus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dextrocardia Situs Solitus", "shortest_name_length": 25}
{"curie": "UMLS:C0475022", "names": ["Renal hematoma", "renal hematoma", "Renal haematoma", "kidney hematoma", "hematoma kidney", "Hematoma of kidney", "hematoma of kidney", "Haematoma of kidney", "Hematoma of kidney (disorder)", "hematoma of kidney (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hematoma of kidney", "shortest_name_length": 14}
{"curie": "MONDO:0019063", "names": ["vascular anomaly", "vascular anomaly or angioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vascular anomaly", "shortest_name_length": 16}
{"curie": "UMLS:C3898108", "names": ["Ocular Contusion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ocular Contusion", "shortest_name_length": 16}
{"curie": "MONDO:0017880", "names": ["RVF", "Zinga fever", "rift valley fever", "Rift Valley fever", "Rift Valley Fever", "Rift valley fever", "RIFT VALLEY FEVER", "Enzootic hepatitis", "Fever, Rift Valley", "fever; Rift Valley", "Rift Valley; fever", "RVF - Rift valley fever", "Rift valley fever (disorder)", "Rift Valley fever (diagnosis)", "Rift Valley fever virus infection", "Viral hemorrhagic fever, Rift valley", "Viral haemorrhagic fever, Rift valley", "Mosquito-borne viral fever, Rift valley"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rift valley fever", "shortest_name_length": 3}
{"curie": "UMLS:C5575829", "names": ["mPV", "Mucosal Dominant Pemphigus Vulgaris", "Mucosal-Dominant Pemphigus Vulgaris"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mucosal-Dominant Pemphigus Vulgaris", "shortest_name_length": 3}
{"curie": "MONDO:0036189", "names": ["OGIN", "OGIN Syndrome", "Oculogastrointestinal-neurodevelopmental syndrome", "oculogastrointestinal-neurodevelopmental syndrome", "OCULOGASTROINTESTINAL NEURODEVELOPMENTAL SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculogastrointestinal-neurodevelopmental syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0677703", "names": ["Stage II Grade 3 Follicular Lymphoma", "noncontiguous stage II grade 3 follicular lymphoma", "Stage II Grade 3 Non-Contiguous Follicular Lymphoma", "Non-Contiguous Stage II Grade III Follicular Lymphoma", "Non-Contiguous Grade III Follicular Lymphoma Stage II", "Stage II Non-Contiguous Follicular Large Cell Lymphoma", "Non-Contiguous Stage II Follicular Large Cell Lymphoma", "Non-Contiguous Follicular Large Cell Lymphoma Stage II", "Ann Arbor Stage II Grade 3 Non-Contiguous Follicular Lymphoma", "noncontiguous stage II grade III follicular large cell lymphoma", "Non-Contiguous Stage II Grade III Follicular Large Cell Lymphoma", "Non-Contiguous Grade III Follicular Large Cell Lymphoma Stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage II Grade 3 Non-Contiguous Follicular Lymphoma", "shortest_name_length": 36}
{"curie": "UMLS:C3889102", "names": ["Product use in unapproved indication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Product use in unapproved indication", "shortest_name_length": 36}
{"curie": "UMLS:C4288304", "names": ["Recurrent Non-Squamous Non-Small Cell Lung Cancer", "Recurrent Lung Non-Squamous Non-Small Cell Carcinoma", "Recurrent Non-Squamous Non-Small Cell Lung Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Lung Non-Squamous Non-Small Cell Carcinoma", "shortest_name_length": 49}
{"curie": "UMLS:C0278504", "names": ["Stage I NSCLC", "stage I NSCLC", "NSCLC, Stage I", "stage I nonsmall cell lung cancer", "non-oat cell lung cancer, stage I", "Stage I Non-Small Cell Lung Cancer", "lung cancer, non-oat cell, stage I", "Lung cancer non-small cell stage I", "nonsmall cell lung cancer, stage I", "Non-small cell lung cancer stage I", "stage I non-small cell lung cancer", "lung cancer, nonsmall cell, stage I", "Stage I Non-Oat Cell Lung Carcinoma", "non-small cell lung cancer, stage I", "Stage I Non-Small Cell Lung Carcinoma", "Stage I Non-Oat Cell Carcinoma of Lung", "Stage I Non-Small Cell Carcinoma of Lung", "Stage I Lung Non-Small Cell Cancer AJCC v7", "Stage I Non-Oat Cell Carcinoma of the Lung", "Stage I Non-Small Cell Lung Cancer AJCC v7", "Stage I Non-Small Cell Carcinoma of the Lung"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-small cell lung cancer stage I", "shortest_name_length": 13}
{"curie": "MONDO:0009338", "names": ["VODI", "VODI syndrome", "hepatic venoocclusive disease with immunodeficiency", "Hepatic venoocclusive disease with immunodeficiency", "HEPATIC VENOOCCLUSIVE DISEASE WITH IMMUNODEFICIENCY", "Hepatic Veno-Occlusive Disease with Immunodeficiency", "veno-occlusive disease and immunodeficiency syndrome", "Veno-Occlusive Disease and Immunodeficiency Syndrome", "hepatic veno-occlusive disease with immunodeficiency", "Familial Veno-Occlusive Disease with Immunodeficiency", "familial veno-occlusive disease with immunodeficiency", "Hepatic veno-occlusive disease-immunodeficiency syndrome", "VODI (veno-occlusive disease, immunodeficiency) syndrome", "hepatic veno-occlusive disease-immunodeficiency syndrome", "Hepatic veno-occlusive disease with immunodeficiency syndrome", "Hepatic veno-occlusive disease with immunodeficiency syndrome (disorder)", "Hepatic veno-occlusive disease with immunodeficiency syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatic veno-occlusive disease-immunodeficiency syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0004774", "names": ["gonococcal iridocyclitis", "iridocyclitis gonococcal", "Gonococcal iridocyclitis", "Gonococcal iridocyclitis (disorder)", "Gonococcal iridocyclitis (diagnosis)", "Neisseria gonorrhoeae iridocyclitis (disease)", "Neisseria gonorrhoeae caused iridocyclitis (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gonococcal iridocyclitis", "shortest_name_length": 24}
{"curie": "MONDO:0044719", "names": ["erythema multiforme major", "erythema multiforme majus", "Erythema Multiforme Major", "Erythema multiforme majus", "Erythema multiforme major", "Erythema multiforme major NOS", "Erythema multiforme major (disorder)", "Erythema exsudativum multiforme majus", "erythema exsudativum multiforme majus", "erythema multiforme major (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythema multiforme major", "shortest_name_length": 25}
{"curie": "UMLS:C0278684", "names": ["Recurrent Parathyroid Cancer", "recurrent parathyroid cancer", "parathyroid cancer, recurrent", "Recurrent Parathyroid Carcinoma", "recurrent parathyroid carcinoma", "parathyroid carcinoma, recurrent", "Recurrent Parathyroid Gland Cancer", "cancer of the parathyroid, recurrent", "Recurrent Parathyroid Gland Carcinoma", "carcinoma of the parathyroid, recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Parathyroid Gland Carcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0015623", "names": ["cavitary myiasis", "Cavitary myiasis", "Infestation of body cavity caused by fly larvae", "Infestation of body cavity caused by fly larvae (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cavitary myiasis", "shortest_name_length": 16}
{"curie": "MONDO:0014974", "names": ["SCFAI", "sudden cardiac failure, alcohol-induced", "sudden Cardiac failure, alcohol-induced", "SUDDEN CARDIAC FAILURE, ALCOHOL-INDUCED", "sudden cardiac failure, alcohol-induced; SCFAI"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sudden cardiac failure, alcohol-induced", "shortest_name_length": 5}
{"curie": "MONDO:0003353", "names": ["heart leiomyosarcoma", "Heart Leiomyosarcoma", "Cardiac leiomyosarcoma", "Cardiac Leiomyosarcoma", "Leiomyosarcoma of Heart", "leiomyosarcoma of heart", "leiomyosarcoma of Heart", "Leiomyosarcoma of the Heart", "leiomyosarcoma of the heart"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heart leiomyosarcoma", "shortest_name_length": 20}
{"curie": "MONDO:0044656", "names": ["Epidermolytic nevus", "epidermolytic nevus", "epidermolytic epidermal nevus", "Epidermolytic epidermal nevus", "Epidermolytic epidermal naevus", "Epidermolytic verrucous epidermal nevus", "epidermolytic verrucous epidermal nevus", "Epidermolytic epidermal nevus (disorder)", "Epidermal nevus with epidermolytic hyperkeratosis", "Epidermolytic epidermal nevus (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolytic nevus", "shortest_name_length": 19}
{"curie": "UMLS:C2981414", "names": ["Stage IV Gastric Gastrointestinal Stromal Tumor", "Stage IV Gastric Gastrointestinal Stromal Tumor AJCC v7", "Stage IV Gastric (Stomach) Gastrointestinal Stromal Tumor (GIST)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Gastric Gastrointestinal Stromal Tumor", "shortest_name_length": 47}
{"curie": "MONDO:0014716", "names": ["SKS", "MINDS syndrome", "MINDS SYNDROME", "SMITH-Kingsmore syndrome", "SMITH-KINGSMORE SYNDROME", "Smith Kingsmore syndrome", "Smith-Kingsmore syndrome", "MACROCEPHALY, SEIZURES, MENTAL RETARDATION, UMBILICAL HERNIA, AND FACIAL DYSMORPHISM", "macrocephaly, seizures, mental retardation, umbilical hernia, and Facial Dysmorphism", "Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome", "macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome", "MACROCEPHALY-INTELLECTUAL DISABILITY-NEURODEVELOPMENTAL DISORDER-SMALL THORAX SYNDROME", "Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome", "macrocephaly, seizures, intellectual disability, umbilical hernia, and Facial Dysmorphism", "MINDS (macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax) syndrome", "Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C2828034", "names": ["Stage IIIA Skin Melanoma AJCC v7", "Stage IIIA Cutaneous (Skin) Melanoma", "Stage IIIA Cutaneous Melanoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Cutaneous Melanoma AJCC v7", "shortest_name_length": 32}
{"curie": "UMLS:C4054706", "names": ["Intermediate Osteogenic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intermediate Osteogenic Neoplasm", "shortest_name_length": 32}
{"curie": "MONDO:0005644", "names": ["amebiases", "AMEBIASIS", "Amebiases", "amebiasis", "Amebiasis", "Amoebiasis", "Amoebiases", "amoebiasis", "Amebiasis NOS", "entamoebiasis", "Amoebiasis NOS", "Amebic infection", "Amebic infections", "Amoebic infection", "Amoebic infections", "amebiasis (diagnosis)", "Amebiasis, unspecified", "Amoebiasis, unspecified", "Disease due to Endamoebidae", "Amebic infection (disorder)", "DISEASES DUE TO ENDAMOEBIDAE", "chronic intestinal amebiasis", "Disease caused by Endamoebidae", "Disease caused by Endamoebidae (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amebiasis", "shortest_name_length": 9}
{"curie": "MONDO:0024432", "names": ["Plexopathy", "plexopathy", "nerve plexus disease", "nerve plexus disorder", "Nerve plexus disorder", "disease of nerve plexus", "disorder of nerve plexus", "Nerve plexus disorder, NOS", "Nerve plexus disorder (disorder)", "nerve plexus disease or disorder", "disease or disorder of nerve plexus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nerve plexus disorder", "shortest_name_length": 10}
{"curie": "MONDO:0011295", "names": ["SCZD7", "SCHIZOPHRENIA 7", "schizophrenia 7", "SCHIZOPHRENIA 7 (disorder)", "schizophrenia 7 with or without an affective disorder", "SCHIZOPHRENIA 7 WITH OR WITHOUT AN AFFECTIVE DISORDER", "SCHIZOPHRENIA SUSCEPTIBILITY LOCUS, CHROMOSOME 13q-RELATED", "schizophrenia susceptibility locus, chromosome 13Q-related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schizophrenia 7", "shortest_name_length": 5}
{"curie": "MONDO:0700163", "names": ["canine Langerhans cell histiocytosis", "Canine Langerhans Cell Histiocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canine Langerhans cell histiocytosis", "shortest_name_length": 36}
{"curie": "UMLS:C0235140", "names": ["DRUG MALADMINISTRATION", "Drug maladministration", "Drug maladministration, NOS", "Effect of drug maladministration", "Effect of drug maladministration, NOS", "Effect of drug maladministration (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Effect of drug maladministration", "shortest_name_length": 22}
{"curie": "MONDO:0014132", "names": ["MMDS3", "IBA57 deficiency", "multiple mitochondrial dysfunctions syndrome 3", "MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3", "multiple mitochondrial dysfunctions syndrome type 3", "Multiple mitochondrial dysfunctions syndrome type 3", "IBA57 fatal multiple mitochondrial dysfunctions syndrome", "MMDS3 - multiple mitochondrial dysfunctions syndrome type 3", "IBA57 (iron-sulfur cluster assembly factor IBA57) deficiency", "Multiple mitochondrial dysfunctions syndrome type 3 (disorder)", "fatal multiple mitochondrial dysfunctions syndrome caused by mutation in IBA57"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple mitochondrial dysfunctions syndrome 3", "shortest_name_length": 5}
{"curie": "MONDO:0009349", "names": ["HPE1", "cyclopia", "Hpe, familial", "ARHINENCEPHALY", "arhinencephaly", "Arhinencephaly", "Demyer sequence", "arrhinencephaly", "Arrhinencephaly", "Arhinencephalies", "holoprosencephaly 1", "Holoprosencephaly 1", "isolated arhinencephaly", "holoprosencephaly type 1", "Holoprosencephaly Type 1", "arhinencephaly (diagnosis)", "holoprosencephaly, familial Alobar", "holoprosencephaly 1, isolated cases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "holoprosencephaly 1", "shortest_name_length": 4}
{"curie": "MONDO:0004280", "names": ["Asymmetric Motor Neuropathy", "asymmetric motor neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "asymmetric motor neuropathy", "shortest_name_length": 27}
{"curie": "MONDO:0017447", "names": ["thumb hypodactyly", "thumb oligodactyly", "congenital absence/hypoplasia of thumb"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital absence/hypoplasia of thumb", "shortest_name_length": 17}
{"curie": "MONDO:0024617", "names": ["Oleoma", "Oil granuloma", "Lipogranuloma", "Oleogranuloma", "lipogranuloma", "Lipid granuloma", "xanthogranuloma", "Xanthogranuloma", "Lipoid granuloma", "lipogranulomatosis", "Lipogranuloma, NOS", "Lipogranulomatosis", "Fibroxanthogranuloma", "Reactive Xanthogranuloma", "Lipogranuloma (disorder)", "Oil granuloma (disorder)", "Xanthogranuloma (disorder)", "Lipogranuloma (morphologic abnormality)", "Xanthogranuloma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "xanthogranuloma", "shortest_name_length": 6}
{"curie": "MONDO:0020362", "names": ["inverse Marcus-Gunn phenomenon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inverse Marcus-Gunn phenomenon", "shortest_name_length": 30}
{"curie": "MONDO:0020704", "names": ["RMD", "rippling muscle disease", "inherited rippling muscle disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited rippling muscle disease", "shortest_name_length": 3}
{"curie": "UMLS:C0477370", "names": ["syndrome; epileptic, generalized", "Other generalized epilepsy and epileptic syndromes", "Other generalised epilepsy and epileptic syndromes", "Other generalized epilepsy and epileptic syndromes NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Other generalized epilepsy and epileptic syndromes", "shortest_name_length": 32}
{"curie": "MONDO:0009725", "names": ["NEM2", "Nemaline Myopathy 2", "NEMALINE MYOPATHY 2", "nemaline myopathy 2", "NEB nemaline myopathy", "congenital myopathy 2", "nemaline myopathy type 2", "nemaline myopathy 2, autosomal recessive", "nemaline myopathy caused by mutation in NEB", "Nemaline myopathy caused by mutation in the nebulin gene"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nemaline myopathy 2", "shortest_name_length": 4}
{"curie": "UMLS:C0158850", "names": ["Fetal malnutrition", "Fetal Malnutrition", "fetal; malnutrition", "Malnutrition, Fetal", "Foetal malnutrition", "Poor fetal nutrition", "Poor foetal nutrition", "Intrauterine malnutrition", "intrauterine; malnutrition", "Poor fetal nutrition (disorder)", "malnutrition; intrauterine or fetal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fetal Malnutrition", "shortest_name_length": 18}
{"curie": "MONDO:0100384", "names": ["AML, t(11;19)(q23;p13.1)", "acute myeloid leukemia, t(11;19)(q23;p13.1)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, t(11;19)(q23;p13.1)", "shortest_name_length": 24}
{"curie": "MONDO:0016650", "names": ["UPD(1)pat", "uniparental disomy paternal chromosome 1", "paternal uniparental disomy of chromosome 1", "Paternal uniparental disomy of chromosome 1", "paternal uniparental disomy of chromosome type 1", "Paternal uniparental disomy of chromosome 1 (disorder)", "Paternal uniparental disomy of chromosome 1 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paternal uniparental disomy of chromosome 1", "shortest_name_length": 9}
{"curie": "UMLS:C1333102", "names": ["Colonic EC-Cell Serotonin Producing Tumor", "Colonic EC-Cell Serotonin-Producing Tumor", "Colonic Enterochromaffin Cell Serotonin-Producing Tumor", "Colon Enterochromaffin Cell Serotonin-Producing Neuroendocrine Tumor", "Colonic Enterochromaffin Cell Serotonin-Producing Neuroendocrine Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colon Enterochromaffin Cell Serotonin-Producing Neuroendocrine Tumor", "shortest_name_length": 41}
{"curie": "UMLS:C5441666", "names": ["Congenital ureterovesical obstruction", "Congenital vesicoureteric obstruction", "Congenital Vesicoureteral Obstruction", "Congenital obstruction of ureteral orifice", "Congenital Ureterovesical Junction Obstruction", "Congenital obstruction of ureterovesical junction", "congenital obstruction of ureterovesical junction", "Congenital obstruction of ureteral orifice (disorder)", "congenital obstruction of ureterovesical junction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital obstruction of ureteral orifice", "shortest_name_length": 37}
{"curie": "UMLS:C0473117", "names": ["Ischemic hepatitis", "HEPATITIS ISCHEMIC", "ischemic hepatitis", "ischaemic hepatitis", "Ischaemic hepatitis", "Ischemic hepatitis (disorder)", "Ischemic hepatitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ischemic hepatitis", "shortest_name_length": 18}
{"curie": "UMLS:C4054385", "names": ["Hepatitis C Virus Associated Nephrotic Syndrome", "Nephrotic Syndrome - Hepatitis C Virus Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - Hepatitis C Virus Associated", "shortest_name_length": 47}
{"curie": "MONDO:0017827", "names": ["mpnst", "MPNST", "Neurilemmosarcoma", "neurofibrosarcoma", "Neurofibrosarcoma", "Neurogenic sarcoma", "Neurilemmosarcomas", "neurogenic sarcoma", "malignant schwannoma", "Malignant Schwannoma", "Malignant schwannoma", "Schwannoma malignant", "malignant neurilemoma", "Schwannoma, Malignant", "Schwannoma, malignant", "Neurilemoma malignant", "Malignant Schwannomas", "Malignant neurilemoma", "Malignant Neurilemoma", "schwannoma, malignant", "Malignant Neurilemomas", "Malignant neurilemmoma", "Neurilemoma, malignant", "malignant neurofibroma", "Malignant neurofibroma", "Malignant Neurilemmoma", "Neurilemoma, Malignant", "malignant neurilemmoma", "Neurilemmoma malignant", "Malignant Neurilemmomas", "Neurilemmoma, Malignant", "Neurilemmoma, malignant", "Malignant Schwannoma, NOS", "neurofibrosarcoma, malignant", "Malig. periph. nerve sheath tum.", "malignant neurilemmoma (diagnosis)", "Malignant Peripheral Nerve Sheath Tumor", "malignant peripheral nerve sheath tumor", "Malignant peripheral nerve sheath tumor", "Peripheral nerve sheath tumor malignant", "Peripheral nerve sheath tumour malignant", "Malignant peripheral nerve sheath tumors", "malignant peripheral nerve sheath tumour", "Malignant peripheral nerve sheath tumour", "Malignant Peripheral Nerve Sheath Tumors", "Peripheral Nerve Sheath Tumors, Malignant", "malignant tumor of peripheral nerve sheath", "Malignant Peripheral Nerve Sheath Neoplasm", "malignant peripheral nerve sheath neoplasm", "malignant neoplasm of peripheral nerve sheath", "malignant tumor of the peripheral nerve sheath", "malignant peripheral nerve sheath tumor (MPNST)", "MPNST - Malignant peripheral nerve sheath tumor", "MPNST - Malignant peripheral nerve sheath tumour", "malignant neoplasm of the peripheral nerve sheath", "malignant neoplasm of the peripheral nerve Sheath", "Malignant peripheral nerve sheath tumor (disorder)", "malignant peripheral nerve sheath tumor (MPNST) (diagnosis)", "malignant peripheral nerve sheath tumor (morphologic abnormality)", "Malignant peripheral nerve sheath tumor (morphologic abnormality)", "malignant peripheral nerve sheath tumor [dup] (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant peripheral nerve sheath tumor", "shortest_name_length": 5}
{"curie": "MONDO:0004661", "names": ["stage 0 trachea carcinoma", "Trachea Carcinoma in situ", "trachea in situ carcinoma", "trachea carcinoma in situ", "Tracheal carcinoma In situ", "Tracheal Carcinoma In Situ", "tracheal carcinoma in situ", "carcinoma in situ of trachea", "Carcinoma in situ of trachea", "Carcinoma in situ of Trachea", "Tracheal carcinoma in situ NOS", "Carcinoma in situ of the Trachea", "carcinoma in situ of the trachea", "Carcinoma in situ of trachea, NOS", "Severe epithelial dysplasia of trachea", "severe epithelial dysplasia of trachea", "Severe Epithelial Dysplasia of Trachea", "Carcinoma in situ of trachea (disorder)", "carcinoma in situ of trachea (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trachea carcinoma in situ", "shortest_name_length": 25}
{"curie": "UMLS:C2347992", "names": ["Advanced Unfavorable Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Unfavorable Hodgkin Lymphoma", "shortest_name_length": 37}
{"curie": "MONDO:0007879", "names": ["Larynx atresia", "larynx atresia", "Larynx Atresia", "atresia; larynx", "larynx; atresia", "laryngeal atresia", "Atresia of larynx", "Laryngeal atresia", "atresia of larynx", "Laryngeal Atresia", "Congenital atresia of larynx", "Congenital Atresia of Larynx", "congenital atresia of larynx", "atresia of larynx (diagnosis)", "congenital atresia of the larynx", "Congenital Atresia of the larynx", "Larynx, Congenital Partial Atresia of", "larynx, congenital partial atresia OF", "LARYNX, CONGENITAL PARTIAL ATRESIA OF", "Congenital atresia of larynx (disorder)", "congenital partial atresia of the larynx"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "larynx atresia", "shortest_name_length": 14}
{"curie": "UMLS:C1335119", "names": ["Mouth Leiomyoma", "Leiomyoma of Mouth", "Oral Cavity Leiomyoma", "Leiomyoma of the Mouth", "Leiomyoma of Oral Cavity", "Leiomyoma of the Oral Cavity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral Cavity Leiomyoma", "shortest_name_length": 15}
{"curie": "MONDO:0019033", "names": ["Scalp rugae", "Scalp folds", "Scalp furrows", "cutis verticis gyrata", "Cutis verticis gyrata", "Cutis gyrata of scalp", "verticis gyrata; cutis", "cutis; verticis gyrata", "Thickening of the scalp", "Cutis verticis gyrata, NOS", "Primary cutis verticis gyrata", "primary cutis verticis gyrata", "Thickened folds on top of scalp", "Cutis verticis gyrata (disorder)", "Furrows in thickened skin on top of scalp"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary cutis verticis gyrata", "shortest_name_length": 11}
{"curie": "UMLS:C1334636", "names": ["Mature Mediastinal Teratoma", "Mediastinal Mature Teratoma", "Mature Teratoma of Mediastinum", "Mature Teratoma of the Mediastinum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mediastinal Mature Teratoma", "shortest_name_length": 27}
{"curie": "UMLS:C0340861", "names": ["EMD", "emd", "PEA", "Pulseless electrical activity", "Pulseless Electrical Activity", "pulseless electrical activity", "Electromechanical Dissociation", "Electromechanical dissociation", "electromechanical dissociation", "ELECTROMECHANICAL DISSOCIATION", "Electro-Mechanical Dissociation", "PEA - Pulseless electrical activity", "electromechanical dissociation (EMD)", "Electromechanical dissociation (disorder)", "electromechanical dissociation (diagnosis)", "Electromechanical Dissociation by EKG Finding", "Electromechanical Dissociation by ECG Finding", "Cardiac arrest with electromechanical dissociation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Electromechanical dissociation", "shortest_name_length": 3}
{"curie": "UMLS:C0343863", "names": ["genital candida", "Genital candida", "candidas genital", "Anogenital thrush", "Genital candidosis", "Moniliasis genital", "moniliasis genital", "MONILIASIS GENITAL", "genital moniliasis", "Genital candidiasis", "Genital Candidiasis", "genital candidiasis", "candidiasis genital", "Candidiasis genital", "Candidiasis, Genital", "Anogenital candidosis", "Anogenital candidiasis", "anogenital candidiasis", "Candidiasis of the genitals", "Anogenital candida infection", "Anogenital candidiasis (disorder)", "anogenital candidiasis (diagnosis)", "candida infection of genital region", "Candida infection of genital region", "Candida infection of genital region (disorder)", "candida infection of genital region (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Candida infection of genital region", "shortest_name_length": 15}
{"curie": "MONDO:0013518", "names": ["CPHD6", "pituitary hormone deficiency, combined, 6", "PITUITARY HORMONE DEFICIENCY, COMBINED, 6", "pituitary hormone deficiency, combined, type 6", "OTX2 combined pituitary hormone deficiencies, genetic form", "combined pituitary hormone deficiencies, genetic form caused by mutation in OTX2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pituitary hormone deficiency, combined, 6", "shortest_name_length": 5}
{"curie": "MONDO:0011940", "names": ["SPINA BIFIDA, SUSCEPTIBILITY TO", "tuberculosis, susceptibility to", "tuberculosis, protection against", "CORONARY ARTERY DISEASE, MODIFIER OF", "tuberculosis infection, protection against", "mycobacterium tuberculosis, susceptibility to", "MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO", "MYCOBACTERIUM TUBERCULOSIS, PROTECTION AGAINST", "Mycobacterium tuberculosis, protection against", "CORONARY ARTERY DISEASE, DEVELOPMENT OF, IN HIV", "Coronary Artery Disease, Development of, in HIV", "MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO (finding)", "MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO INFECTION BY", "Mycobacterium tuberculosis, susceptibility to infection by"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mycobacterium tuberculosis, susceptibility to", "shortest_name_length": 31}
{"curie": "UMLS:C0268147", "names": ["Gsdix", "Gsd Ix", "GSD IX", "GSD type 9", "GSD type IX", "Phk Deficiency", "Glycogenosis viiia", "Glycogenosis type 9", "Glycogenosis type IX", "Glycogen storage disease VIII", "Glycogen storage disease type 9", "Phosphorylase Kinase Deficiency", "glycogen storage disease type IX", "Glycogen Storage Disease Type Ix", "Glycogen Storage Disease Type IX", "Glycogen storage disease type IX", "Phosphorylase B Kinase Deficiency", "Glycogen storage disease, type IX", "Gycogenosis due to PhK deficiency", "hepatic phosphorylase kinase deficiency", "Hepatic phosphorylase kinase deficiency", "Phosphorylase kinase deficiency of liver", "Glycogen phosphorylase kinase deficiency", "GSD due to phosphorylase kinase deficiency", "Glycogen storage disease type IX (disorder)", "glycogen storage disease type IX (diagnosis)", "PHK - Hepatic phosphorylase kinase deficiency", "Glycogen storage disease due to PhK deficiency", "Hepatic glycogen phosphorylase kinase deficiency", "Glycogenosis due to phosphorylase kinase deficiency", "Glycogen storage disease due to phosphorylase kinase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Glycogen storage disease, type IX", "shortest_name_length": 5}
{"curie": "MONDO:0010962", "names": ["PPKNE", "NEPPK", "TYLOSIS", "tylosis", "diffuse NEPPK", "Thost-Unna disease", "Unna-Thost Syndrome", "Unna-Thost syndrome", "Thost-Unna syndrome", "Thost-Unna Syndrome", "PPK diffusa circumscripta", "Unna-Thost palmoplantar keratoderma", "Thost-Unna palmoplantar keratoderma", "Nonepidermolytic palmoplantar keratoderma", "Nonepidermolytic Palmoplantar Keratoderma", "NONEPIDERMOLYTIC PALMOPLANTAR KERATODERMA", "nonepidermolytic palmoplantar keratoderma", "keratoderma, nonepidermolytic palmoplantar", "KERATODERMA, NONEPIDERMOLYTIC PALMOPLANTAR", "Non-epidermolytic palmoplantar keratoderma", "PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC", "Keratoderma, Nonepidermolytic Palmoplantar", "Palmoplantar Keratoderma, Nonepidermolytic", "non-epidermolytic palmoplantar keratoderma", "palmoplantar keratoderma, nonepidermolytic", "Nonepidermolytic palmoplantar hyperkeratosis", "Diffuse palmoplantar keratoderma, Bothnian type", "diffuse palmoplantar keratoderma, Bothnian type", "NEPPK Nonepidermolytic Palmoplantar Keratoderma", "diffuse nonepidermolytic palmoplantar keratoderma", "KRT1-related diffuse nonepidermolytic keratoderma", "diffuse nonepidermolytic palmomplantar keratoderma", "Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type", "Autosomal dominant diffuse palmoplantar keratoderma, Norrbotten type", "autosomal dominant diffuse palmoplantar keratoderma, Norrbotten type", "Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diffuse nonepidermolytic palmoplantar keratoderma", "shortest_name_length": 5}
{"curie": "MONDO:0003327", "names": ["PNS ganglioneuroblastoma", "PNS Ganglioneuroblastoma", "Peripheral Ganglioneuroblastoma", "peripheral ganglioneuroblastoma", "Peripheral Nervous System Ganglioneuroblastoma", "peripheral nervous system ganglioneuroblastoma", "peripheral nervous system ganglioneuroblastoma (disease)", "ganglioneuroblastoma (disease) of peripheral nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peripheral ganglioneuroblastoma", "shortest_name_length": 24}
{"curie": "UMLS:C5238240", "names": ["Locally Advanced Ovarian Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Ovarian Carcinoma", "shortest_name_length": 34}
{"curie": "UMLS:C1336455", "names": ["Follicular lymphoma stage I", "Stage I Follicular Lymphoma", "Ann Arbor Stage I Follicular Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Follicular lymphoma stage I", "shortest_name_length": 27}
{"curie": "MONDO:0009769", "names": ["OPC DWARFISM", "OPC dwarfism", "OCULOPALATOCEREBRAL SYNDROME", "Oculopalatocerebral Dwarfism", "oculopalatocerebral dwarfism", "Oculopalatocerebral syndrome", "OCULOPALATOCEREBRAL DWARFISM", "Oculopalatocerebral Syndrome", "oculopalatocerebral syndrome", "oculo-palato-cerebral dwarfism", "Oculo-palato-cerebral dwarfism", "oculo-palato-cerebral syndrome", "Oculo-palato-cerebral syndrome", "Oculopalatocerebral syndrome (disorder)", "Oculopalatocerebral syndrome (diagnosis)", "congenital malformation syndromes oculopalatocerebral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculo-palato-cerebral syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0005419", "names": ["metamphetamine dependence"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metamphetamine dependence", "shortest_name_length": 25}
{"curie": "MONDO:0016828", "names": ["ARSA", "Congenital sideroblastic anemia", "congenital sideroblastic anemia", "autosomal recessive sideroblastic anemia", "Autosomal recessive sideroblastic anemia", "sideroblastic anemia, autosomal recessive", "Autosomal recessive sideroblastic anaemia", "Autosomal recessive sideroblastic anemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive sideroblastic anemia", "shortest_name_length": 4}
{"curie": "UMLS:C0278776", "names": ["recurent childhood AML", "relapsed childhood AML", "Relapsed Childhood AML", "relapsed pediatric AML", "Relapsed Pediatric AML", "childhood AML, relapsed", "Recurrent Pediatric AML", "relapsed pediatric ANLL", "Recurrent Childhood AML", "relapsed childhood ANLL", "recurrent childhood ANLL", "AML, relapsed, childhood", "childhood AML, recurrent", "AML, relapsed, pediatric", "AML, recurrent, pediatric", "AML, recurrent, childhood", "ANLL, relapsed, pediatric", "ANLL, relapsed, childhood", "ANLL, recurrent, childhood", "ANLL, recurrent, pediatric", "Recurrent Acute Myeloid Leukemia (AML)", "relapsed childhood acute myeloid leukemia", "Relapsed Childhood Acute Myeloid Leukemia", "relapsed pediatric acute myeloid leukemia", "Relapsed Pediatric Acute Myeloid Leukemia", "myeloid leukemia, relapsed childhood acute", "recurrent childhood acute myeloid leukemia", "myeloid leukemia, relapsed pediatric acute", "pediatric acute myeloid leukemia, relapsed", "childhood acute myeloid leukemia, relapsed", "pediatric leukemia, acute myeloid relapsed", "leukemia, relapsed childhood acute myeloid", "Recurrent Childhood Acute Myeloid Leukemia", "childhood leukemia, acute myeloid relapsed", "recurrent pediatric acute myeloid leukemia", "Recurrent Pediatric Acute Myeloid Leukemia", "acute myeloid leukemia, relapsed, childhood", "leukemia, recurrent childhood acute myeloid", "childhood acute myeloid leukemia, recurrent", "acute myeloid leukemia, recurrent, childhood", "Relapsed Pediatric Acute Myelocytic Leukemia", "Relapsed Childhood Acute Myelocytic Leukemia", "Recurrent Childhood Acute Myelocytic Leukemia", "Relapsed Pediatric Acute Myelogenous Leukemia", "Relapsed Childhood Acute Myelogenous Leukemia", "Recurrent Pediatric Acute Myelocytic Leukemia", "Recurrent Pediatric Acute Myelogenous Leukemia", "Relapsed Childhood Acute Myeloblastic Leukemia", "Recurrent Childhood Acute Myelogenous Leukemia", "Relapsed Pediatric Acute Myeloblastic Leukemia", "Recurrent Pediatric Acute Myeloblastic Leukemia", "Recurrent Childhood Acute Myeloblastic Leukemia", "relapsed childhood acute nonlymphocytic leukemia", "relapsed pediatric acute nonlymphocytic leukemia", "childhood acute nonlymphocytic leukemia, relapsed", "recurrent childhood acute nonlymphocytic leukemia", "nonlymphocytic leukemia, relapsed pediatric acute", "leukemia, relapsed childhood acute nonlymphocytic", "recurrent pediatric acute nonlymphocytic leukemia", "nonlymphocytic leukemia, relapsed childhood acute", "pediatric acute nonlymphocytic leukemia, relapsed", "pediatric leukemia, acute nonlymphocytic relapsed", "childhood leukemia, acute nonlymphocytic relapsed", "Recurrent Childhood Acute Non-Lymphocytic Leukemia", "leukemia, reucrrent childhood acute nonlymphocytic", "acute nonlymphocytic leukemia, relapsed, childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "recurrent childhood acute myeloid leukemia", "shortest_name_length": 22}
{"curie": "UMLS:C1262018", "names": ["Graft failure", "Graft Failure", "Graft Rejection", "failure transplant", "transplant failure", "Transplant failure", "failure; transplant", "transplant; failure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Graft failure", "shortest_name_length": 13}
{"curie": "UMLS:C0008625", "names": ["Aberrant Chromosome", "abnormal chromosome", "abnormal chromosomes", "Chromosome Anomalies", "chromosomal anomalies", "chromosome aberration", "Chromosome Aberration", "Chromosome Aberrations", "chromosomal aberration", "Chromosome Abnormality", "Cytogenetic Aberration", "Aberration, Chromosome", "Chromosome Alterations", "CHROMOSOME ABNORMALITY", "chromosome aberrations", "chromosome abnormality", "Chromosomal Aberration", "chromosomal abnormality", "Chromosomal Alterations", "Aberrations, Chromosome", "Cytogenetic Aberrations", "chromosomal aberrations", "Chromosomal Abnormality", "Aberration, Chromosomal", "Cytogenetic Abnormality", "Abnormality, Chromosome", "Chromosomal Aberrations", "Aberration, Cytogenetic", "Abnormality, Chromosomal", "chromosome abnormalities", "Chromosome Abnormalities", "Chromosome abnormalities", "Abnormality, Cytogenetic", "Aberrations, Cytogenetic", "Aberrations, Chromosomal", "Abnormalities, Chromosome", "chromosomal abnormalities", "Chromosomal Abnormalities", "Chromosomal abnormalities", "Cytogenetic Abnormalities", "Abnormalities, Cytogenetic", "Abnormalities, Chromosomal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chromosome Aberrations", "shortest_name_length": 19}
{"curie": "UMLS:C4528640", "names": ["Stage III Low-CSD Melanoma AJCC v7", "Stage III Superficial Spreading Melanoma AJCC v7", "Stage III Superficial Spreading Cutaneous (Skin) Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Low-CSD Melanoma AJCC v7", "shortest_name_length": 34}
{"curie": "MONDO:0003400", "names": ["childhood yolk Sac tumor", "pediatric yolk Sac tumor", "Pediatric Yolk Sac Tumor", "pediatric Yolk Sac tumor", "Childhood Yolk Sac Tumor", "paediatric Yolk Sac tumour", "Childhood Yolk Sac Neoplasm", "childhood yolk Sac neoplasm", "pediatric yolk Sac neoplasm", "Pediatric Yolk Sac Neoplasm", "Childhood Endodermal Sinus Tumor", "childhood endodermal sinus tumor", "childhood endodermal sinus tumour", "Childhood Endodermal Sinus Neoplasm", "pediatric endodermal sinus neoplasm", "Pediatric Endodermal Sinus Neoplasm", "childhood endodermal sinus neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood endodermal sinus tumor", "shortest_name_length": 24}
{"curie": "MONDO:0012245", "names": ["DEE3", "EIEE3", "Early Myoclonic Encephalopathy", "early infantile epileptic encephalopathy 3", "Epileptic Encephalopathy, Early Infantile, 3", "developmental and epileptic encephalopathy 3", "epileptic encephalopathy, early infantile, 3", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 3", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 3", "developmental and epileptic encephalopathy, 3", "SLC25A22 early infantile epileptic encephalopathy", "epileptic encephalopathy, early infantile, type 3", "Myoclonic Epilepsy, Neonatal, With Suppression-Burst Pattern", "early infantile epileptic encephalopathy caused by mutation in SLC25A22"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 3", "shortest_name_length": 4}
{"curie": "MONDO:0009798", "names": ["PRIMS", "PRIMROSE SYNDROME", "Primrose syndrome", "intellectual disability-cataracts-calcified pinnae-myopathy syndrome", "Intellectual disability-cataracts-calcified pinnae-myopathy syndrome", "intellectual disability, cataract, calcified pinna, myopathy syndrome", "Intellectual disability, cataract, calcified pinna, myopathy syndrome", "ossified ear cartilages-mental deficiency-muscle wasting-bony changes syndrome", "ossified EAR cartilages with mental deficiency, muscle wasting, and BONY changes", "Intellectual disability, cataract, calcified pinna, myopathy syndrome (disorder)", "OSSIFIED EAR CARTILAGES WITH MENTAL DEFICIENCY, MUSCLE WASTING, AND BONY CHANGES", "intellectual disability, cataract, calcified pinna, myopathy syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primrose syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0010794", "names": ["NARP", "NARP syndrome", "NARP SYNDROME", "Neuropathy ataxia and retinitis pigmentosa", "neuropathy, ataxia and retinitis pigmentosa", "Neuropathy, Ataxia, and Retinitis Pigmentosa", "neuropathy, ataxia, and retinitis pigmentosa", "NEUROPATHY, ATAXIA, AND RETINITIS PIGMENTOSA", "neuropathy-ataxia-retinitis pigmentosa syndrome", "Neuropathy-ataxia-retinitis pigmentosa syndrome", "neuropathy ataxia retinitis pigmentosa syndrome", "Neuropathy, Ataxia, Retinitis Pigmentosa syndrome", "Neuropathy, ataxia, retinitis pigmentosa syndrome", "Neurogenic muscle weakness, ataxia and retinitis pigmentosa", "Neuropathy, Ataxia and Retinitis Pigmentosa (NARP syndrome)", "Neurogenic Muscle Weakness, Ataxia, and Retinitis Pigmentosa", "Neurogenic muscle weakness-ataxia-retinitis pigmentosa syndrome", "neurogenic muscle weakness-ataxia-retinitis pigmentosa syndrome", "NARP - Neurogenic muscle weakness, ataxia and retinitis pigmentosa", "Neurogenic muscle weakness, ataxia and retinitis pigmentosa (disorder)", "neurogenic muscle weakness, ataxia and retinitis pigmentosa (NARP) syndrome", "neurogenic muscle weakness, ataxia and retinitis pigmentosa (NARP) syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "NARP syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0012849", "names": ["JBTS9", "Joubert syndrome 9", "JOUBERT SYNDROME 9", "Joubert Syndrome 9", "Joubert syndrome type 9", "CC2D2A Joubert syndrome", "JOUBERT SYNDROME 9/15, DIGENIC", "Joubert syndrome 9/15, digenic", "Joubert syndrome caused by mutation in CC2D2A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome 9", "shortest_name_length": 5}
{"curie": "MONDO:0017065", "names": ["lumbosacral spina bifida aperta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lumbosacral spina bifida aperta", "shortest_name_length": 31}
{"curie": "UMLS:C5556868", "names": ["Jejunal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jejunal Carcinoma", "shortest_name_length": 17}
{"curie": "MONDO:0005238", "names": ["Round Cell Liposarcoma", "Round cell liposarcoma", "round cell liposarcoma", "round cell; liposarcoma", "Lipoblastic liposarcoma", "liposarcoma; round cell", "Cellular Myxoid Liposarcoma", "cellular myxoid liposarcoma", "round cell liposarcoma (diagnosis)", "round cell liposarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "round cell liposarcoma", "shortest_name_length": 22}
{"curie": "MONDO:0021364", "names": ["oropharynx tumor", "Oropharynx Neoplasm", "Tumor of Oropharynx", "tumor of oropharynx", "Tumor of oropharynx", "Oropharyngeal Tumor", "oropharyngeal tumor", "oropharynx neoplasm", "Tumour of oropharynx", "Neoplasm, Oropharynx", "Oropharynx Neoplasms", "Neoplasms, Oropharynx", "Oropharyngeal neoplasm", "Neoplasm of oropharynx", "oropharyngeal neoplasm", "neoplasm of oropharynx", "Neoplasm of Oropharynx", "Oropharyngeal Neoplasm", "oropharyngeal neoplasms", "Neoplasm, Oropharyngeal", "Tumor of the Oropharynx", "tumor of the oropharynx", "Oropharyngeal Neoplasms", "oral pharyngeal neoplasm", "Neoplasms, Oropharyngeal", "Neoplasm of the Oropharynx", "neoplasm of the oropharynx", "oropharynx neoplasm (disease)", "oropharyngeal tumor or cancer", "oral pharyngeal tumor or cancer", "Neoplasm of oropharynx (disorder)", "neoplasm of oropharynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neoplasm of oropharynx", "shortest_name_length": 16}
{"curie": "MONDO:0009019", "names": ["CHED", "CHED2", "CHEDII", "CHED2, FORMERLY", "CHED2, formerly", "autosomal recessive CHED", "Autosomal recessive CHED", "Maumenee corneal dystrophy", "corneal endothelial dystrophy", "CORNEAL ENDOTHELIAL DYSTROPHY", "CORNEAL ENDOTHELIAL DYSTROPHY 2", "Corneal Endothelial Dystrophy 2", "corneal endothelial dystrophy 2", "corneal endothelial dystrophy type 2", "Corneal endothelial dystrophy type 2", "infantile hereditary endothelial dystrophy", "Infantile hereditary endothelial dystrophy", "Congenital hereditary endothelial dystrophy type 2", "corneal endothelial dystrophy, autosomal recessive", "congenital hereditary endothelial dystrophy type 2", "Congenital hereditary endothelial dystrophy type II", "congenital hereditary endothelial dystrophy, CHED 2", "congenital hereditary endothelial dystrophy type II", "corneal endothelial dystrophy 2, autosomal recessive", "CORNEAL DYSTROPHY, CONGENITAL HEREDITARY ENDOTHELIAL", "corneal dystrophy, congenital hereditary endothelial", "Corneal dystrophy, congenital hereditary endothelial", "congenital hereditary endothelial dystrophy of cornea", "CONGENITAL HEREDITARY ENDOTHELIAL DYSTROPHY OF CORNEA", "CHED II - Congenital hereditary endothelial dystrophy II", "Congenital hereditary endothelial dystrophy of the cornea", "congenital hereditary endothelial dystrophy of the cornea", "Congenital hereditary endothelial dystrophy type 2 (disorder)", "CORNEAL ENDOTHELIAL DYSTROPHY 2, AUTOSOMAL RECESSIVE, FORMERLY", "corneal endothelial dystrophy 2, autosomal recessive, formerly", "autosomal recessive congenital hereditary endothelial dystrophy", "congenital hereditary endothelial dystrophy, CHED 2 (diagnosis)", "Autosomal recessive congenital hereditary endothelial dystrophy", "CHED2 Congenital hereditary endothelial dystrophy of the cornea 2", "Congenital hereditary endothelial dystrophy, autosomal recessive form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital hereditary endothelial dystrophy of cornea", "shortest_name_length": 4}
{"curie": "MONDO:0001582", "names": ["Cicatricial ectropion", "cicatricial ectropion", "Cicatricial ectropion (disorder)", "cicatricial ectropion (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cicatricial ectropion", "shortest_name_length": 21}
{"curie": "UMLS:C0033270", "names": ["Retained secundines", "Retained secundines (disorder)", "conception of products retained", "RETAINED PRODUCTS OF CONCEPTION", "Retained secundines (diagnosis)", "retained products of conception", "Retained products of conception", "Products of conception, retained", "Retained products of conception, NOS", "RPC - Retained products of conception", "RPOC - Retained products of conception", "Retained products of conception (disorder)", "Retained products of conception (diagnosis)", "pregnancy complications disorder of product of conception retained", "pregnancy complications disorder of product of conception retained secundines"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retained products of conception", "shortest_name_length": 19}
{"curie": "MONDO:0001168", "names": ["hemiplegia spastic", "Spastic hemiplegia", "SPASTIC HEMIPLEGIA", "spastic hemiplegia", "Spastic Hemiplegia", "hemiplegia; spastic", "Hemiplegia, Spastic", "Spastic hemiparesis", "Spastic Hemiplegias", "spastic; hemiplegia", "Hemiplegias, Spastic", "Congenital hemiplegia", "congenital hemiplegia", "hemiplegia; hypertonic", "hemiplegia; congenital", "hypertonic; hemiplegia", "congenital; hemiplegia", "cerebral hemiplegic palsy", "hemiplegic cerebral palsy", "Hemiplegic cerebral palsy", "Spastic hemiplegia syndrome", "Spastic hemiplegia (disorder)", "spastic hemiplegia (diagnosis)", "spastic hemiplegic cerebral palsy", "Spastic hemiplegic cerebral palsy", "hemiplegic infantile cerebral palsy", "Hemiplegic infantile cerebral palsy", "infantile hemiplegic cerebral palsy", "congenital hemiplegic cerebral palsy", "Infantile cerebral palsy, hemiplegic", "Hemiplegic cerebral palsy (disorder)", "hemiplegic cerebral palsy (diagnosis)", "Spastic hemiplegia affecting unspecified side", "Spastic hemiplegia, affecting unspecified side", "infantile (postnatal) hemiplegic cerebral palsy", "infantile hemiplegic cerebral palsy (diagnosis)", "congenital hemiplegic cerebral palsy (diagnosis)", "Spastic hemiplegia and hemiparesis affecting unspecified side"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic hemiplegia", "shortest_name_length": 18}
{"curie": "MONDO:0019881", "names": ["trisomy 6q", "6q+ syndrome", "trisomy 6qter", "Trisomy 6qter", "dup(6q) syndrome", "distal trisomy 6q", "Distal trisomy 6q", "partial trisomy 6q", "Trisomy 6q, Partial", "6q+ Syndrome, Partial", "Distal Duplication 6q", "distal duplication 6q", "Distal duplication 6q", "chromosome 6q trisomy", "distal trisomy type 6q", "6q duplication syndrome", "duplication 6q syndrome", "Telomeric duplication 6q", "telomeric duplication 6q", "Chromosome 6, Trisomy 6q2", "6q partial trisomy syndrome", "Distal trisomy 6q (disorder)", "Trisomy 6q Syndrome, Partial", "Distal trisomy 6q (diagnosis)", "Chromosome 6, partial trisomy 6q", "chromosome 6q duplication syndrome", "6q partial trisomy syndrome (disorder)", "6q partial trisomy syndrome (diagnosis)", "anomaly of chromosome pair 6q partial trisomy syndrome", "anomaly of chromosome pair 6q partial trisomy syndrome distal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal trisomy 6q", "shortest_name_length": 10}
{"curie": "MONDO:0011239", "names": ["MACOM", "MACOM syndrome", "MACROPHTHALMIA, COLOBOMATOUS, WITH MICROCORNEA", "macrophthalmia, colobomatous, with microcornea", "Macrophthalmia, Colobomatous, with Microcornea", "Colobomatous macrophthalmia-microcornea syndrome", "colobomatous macrophthalmia-microcornea syndrome", "Colobomatous macrophthalmia with microcornea syndrome", "MACOM (macrophthalmia colobomatous with microcornea) syndrome", "Colobomatous macrophthalmia with microcornea syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colobomatous macrophthalmia-microcornea syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0010913", "names": ["CAROLI DISEASE", "caroli disease", "Caroli Disease", "Caroli disease", "carolis disease", "Carolis Disease", "Disease, Caroli", "Caroli syndrome", "Caroli Syndrome", "Caroli's Disease", "caroli's disease", "Carolis Syndrome", "Caroli's disease", "Caroli's Syndrome", "Disease, Caroli's", "Syndrome, Caroli's", "Caroli disease isolated", "CAROLI disease, isolated", "CAROLI DISEASE, ISOLATED", "Caroli Disease, Isolated", "Caroli disease (disorder)", "Valvular gallbladder disease", "Dilatation intrahepatic duct congenital", "cystic dilatation of the intrahepatic biliary tree", "Cystic dilatation of the intrahepatic biliary tree", "Congenital dilatation of lobar intrahepatic bile duct", "congenital polycystic dilatation of intrahepatic bile ducts", "Congenital polycystic dilatation of intrahepatic bile ducts", "Congenital dilatation of lobar intrahepatic bile duct (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Caroli disease", "shortest_name_length": 14}
{"curie": "MONDO:0007609", "names": ["GGF1", "HGF1", "GINGF", "GINGF1", "gingival fibromatosis, 1", "fibromatosis, gingival, 1", "FIBROMATOSIS, GINGIVAL, 1", "SOS1 gingival fibromatosis", "fibromatosis, gingival, type 1", "Fibromatosis, Gingival, Type 1", "fibromatosis, gingival, hereditary", "hereditary gingival fibromatosis, 1", "fibromatosis gingival, hereditary, 1", "SOS1 hereditary gingival fibromatosis", "gingival fibromatosis caused by mutation in SOS1", "hereditary gingival fibromatosis caused by mutation in SOS1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibromatosis, gingival, 1", "shortest_name_length": 4}
{"curie": "MONDO:0001955", "names": ["protozoal dysentery", "Other specified protozoal intestinal diseases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "protozoal dysentery", "shortest_name_length": 19}
{"curie": "MONDO:0024294", "names": ["infectious skin disease", "infectious skin diseases", "skin disease, infectious", "disease, infectious skin", "Skin Diseases, Infectious", "diseases, infectious skin", "skin disorder caused by infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin disorder caused by infection", "shortest_name_length": 23}
{"curie": "MONDO:0002490", "names": ["PBS", "sarcoma breast", "Breast Sarcoma", "Breast sarcoma", "breast sarcoma", "breast sarcomas", "sarcoma of breast", "Sarcoma of breast", "Sarcoma of Breast", "Sarcoma of the Breast", "sarcoma of the breast", "Sarcoma of breast (disorder)", "sarcoma of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast sarcoma", "shortest_name_length": 3}
{"curie": "UMLS:C4725616", "names": ["Refractory Ovarian Endometrioid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Ovarian Endometrioid Adenocarcinoma", "shortest_name_length": 46}
{"curie": "UMLS:C0406175", "names": ["Chafed skin", "chafed skin", "skin chafing", "chafing skin", "chafing of skin", "Chafing of skin", "Chafing of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chafing of skin", "shortest_name_length": 11}
{"curie": "UMLS:C0035281", "names": ["Retention Cyst", "retention cyst", "Retention cyst", "Retention cysts", "cysts retention", "Retention cyst, NOS", "Retention cyst (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Retention cyst", "shortest_name_length": 14}
{"curie": "UMLS:C4552687", "names": ["Stage IA Fallopian Tube Cancer", "Stage IA Fallopian Tube Cancer AJCC v8", "Stage IA Fallopian Tube Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Fallopian Tube Cancer AJCC v8", "shortest_name_length": 30}
{"curie": "MONDO:0012171", "names": ["MARFANOID HABITUS WITH SITUS INVERSUS", "Marfanoid Habitus with Situs Inversus", "marfanoid habitus with situs inversus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "marfanoid habitus with situs inversus", "shortest_name_length": 37}
{"curie": "UMLS:C5447284", "names": ["Unresectable Nasal Cavity Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Nasal Cavity Squamous Cell Carcinoma", "shortest_name_length": 49}
{"curie": "MONDO:0001567", "names": ["Renal calcinosis", "Nephrocalcinoses", "nephrocalcinosis", "CALCINOSIS RENAL", "Calcinosis renal", "NEPHROCALCINOSIS", "Nephrocalcinosis", "Renal calcification", "hypercalcemic nephropathy", "Nephrocalcinosis (disorder)", "nephrocalcinosis (diagnosis)", "Increased calcium level in kidney", "Too much calcium deposited in kidneys"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrocalcinosis", "shortest_name_length": 16}
{"curie": "MONDO:0007328", "names": ["choroidal osteoma, bilateral", "CHOROIDAL OSTEOMA, BILATERAL", "Choroidal Osteoma, Bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "choroidal osteoma, bilateral", "shortest_name_length": 28}
{"curie": "MONDO:0002493", "names": ["Prostate Acinar Adenocarcinoma", "prostate acinar adenocarcinoma", "Acinar Prostate Adenocarcinoma", "acinar prostate adenocarcinoma", "prostatic acinar adenocarcinoma", "Prostatic Acinar Adenocarcinoma", "acinar adenocarcinoma of prostate", "Acinar Adenocarcinoma of Prostate", "acinar adenocarcinoma of the prostate", "Acinar Adenocarcinoma of the Prostate", "Prostate Adenocarcinoma, Acinar Type/NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostatic acinar adenocarcinoma", "shortest_name_length": 30}
{"curie": "UMLS:C5442260", "names": ["Oral Melanocytic Nevus", "Oral melanocytic nevus", "Oral melanocytic naevus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral melanocytic nevus", "shortest_name_length": 22}
{"curie": "UMLS:C2981352", "names": ["Stage IV Lung Cancer", "Stage IV Lung Cancer AJCC v6", "Stage IV Lung Carcinoma AJCC v6", "Stage IV Carcinoma of Lung AJCC v6", "Stage IV Carcinoma of the Lung AJCC v6", "Unspecified Stage IV Carcinoma of Lung AJCC v6", "Unspecified Stage IV Carcinoma of the Lung AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Lung Cancer AJCC v6", "shortest_name_length": 20}
{"curie": "MONDO:0015257", "names": ["sino-auricular heart block"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sino-auricular heart block", "shortest_name_length": 26}
{"curie": "UMLS:C5205065", "names": ["Refractory Diffuse Large B-Cell Lymphoma Germinal Center B-Cell Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Diffuse Large B-Cell Lymphoma Germinal Center B-Cell Type", "shortest_name_length": 68}
{"curie": "UMLS:C5206768", "names": ["Refractory Urinary System Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Urinary System Carcinoma", "shortest_name_length": 35}
{"curie": "MONDO:0019565", "names": ["Von Willebrand", "ANGIOHEMOPHILIA", "Angiohemophilia", "angiohemophilia", "Angiohaemophilia", "pseudohemophilia", "PSEUDOHEMOPHILIA", "Angiohemophilias", "Pseudohemophilia", "Pseudohaemophilia", "Willebrand-Jürgens", "Angiohemophilia, A", "Angiohemophilia, B", "vascular hemophilia", "Vascular hemophilia", "VASCULAR HEMOPHILIA", "Vascular Hemophilia", "Vascular Hemophilias", "Hemophilia, Vascular", "vascular; hemophilia", "Vascular haemophilia", "HEMOPHILIA, VASCULAR", "hemophilia; vascular", "Von Willebrand disease", "VON WILLEBRAND DISEASE", "von Willebrand disease", "disease von willebrand", "von willebrand disease", "von Willebrand Disease", "Pseudohemophilia type B", "von Willebrand Diseases", "von willebrand disorder", "von Willebrand disorder", "Disease;Von Willebrands", "Von Willebrand Disorder", "disease von willebrands", "VON WILLEBRANDS DISEASE", "Von Willebrands disease", "von willebrands disease", "Disorder, Von Willebrand", "von willebrand's disease", "Von Willebrand's disease", "VON WILLEBRAND'S DISEASE", "Pseudohaemophilia type B", "von Willebrand's disease", "von Willebrand's Disease", "diseases von willebrand's", "vascular pseudohemophilia", "von Willebrand's Diseases", "Vascular Pseudohemophilia", "Vascular pseudohemophilia", "Factor VIII Rag deficiency", "Vascular Pseudohemophilias", "vascular; pseudohemophilia", "pseudohemophilia; vascular", "Pseudohemophilia, Vascular", "Constitutional thrombopathy", "Pseudohemophilias, Vascular", "von Willebrand disease, NOS", "WILLEBRAND-JUERGENS DISEASE", "Minot-von Willebrand-Jürgens", "thrombopathy; constitutional", "constitutional; thrombopathy", "von Willebrand-Jrgens disease", "vWD - von Willebrand's disease", "von Willebrand-Jurgens disease", "thrombopathy; Willebrand-Jürgens", "Willebrand-Jürgens; thrombopathy", "von Willebrand's-Jurgens' disease", "Hereditary von Willebrand disease", "hereditary von Willebrand disease", "congenital von willebrand disease", "Von willebrand factor, deficiency", "von Willebrand disorder (disorder)", "Von Willebrand's Factor Deficiency", "Von Willebrand's factor deficiency", "von Willebrand disease (diagnosis)", "Von Willebrand disease, unspecified", "congenital von willebrand's disease", "vascular pseudohemophilia (diagnosis)", "Factor VIII deficiency with vascular defect", "hereditary von Willebrand disease (hereditary or acquired)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary von Willebrand disease", "shortest_name_length": 14}
{"curie": "MONDO:0012796", "names": ["RP41", "RP 41", "retinitis pigmentosa 41", "Retinitis Pigmentosa 41", "RETINITIS PIGMENTOSA 41", "PROM1 retinitis pigmentosa", "retinitis pigmentosa type 41", "RETINITIS PIGMENTOSA 41 (disorder)", "retinitis pigmentosa caused by mutation in PROM1", "Retinal Degeneration, Autosomal Recessive, Prominin-Related", "retinal Degeneration, autosomal recessive, prominin-related", "RETINAL DEGENERATION, AUTOSOMAL RECESSIVE, PROMININ-RELATED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 41", "shortest_name_length": 4}
{"curie": "UMLS:C0278764", "names": ["DUL, adult", "Burkitt Lymphoma", "adult SNC lymphoma", "SNC lymphoma, adult", "adult Burkitt lymphoma", "Adult Burkitt Lymphoma", "Adult Burkitt's Lymphoma", "Adult Small Non-Cleaved Cell Lymphoma", "small noncleaved cell lymphoma, adult", "lymphoma, small noncleaved cell, adult", "diffuse undifferentiated lymphoma, adult", "lymphoma, diffuse undifferentiated, adult", "adult diffuse small noncleaved cell/Burkitt's lymphoma", "Adult Diffuse Small Non-Cleaved Cell/Burkitt's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Burkitt Lymphoma", "shortest_name_length": 10}
{"curie": "UMLS:C0280322", "names": ["Postcricoid Epidermoid Carcinoma", "Postcricoid Squamous Cell Carcinoma", "Epidermoid Carcinoma of Postcricoid Area", "Squamous Cell Carcinoma of Postcricoid Area", "Epidermoid Carcinoma of the Postcricoid Area", "Squamous Cell Carcinoma of the Postcricoid Area"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postcricoid Squamous Cell Carcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C5420166", "names": ["Pharyngeal Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pharyngeal Lymphoma", "shortest_name_length": 19}
{"curie": "MONDO:0019604", "names": ["Acquired Fanconi syndrome secondary to monoclonal gammopathy", "acquired Fanconi syndrome secondary to monoclonal gammopathy", "Acquired monoclonal Ig light chain-associated Fanconi syndrome", "acquired monoclonal Ig light chain-associated Fanconi syndrome", "acquired monoclonal immunoglobulin light chain-associated Fanconi syndrome", "Acquired monoclonal immunoglobulin light chain-associated Fanconi syndrome", "Acquired monoclonal immunoglobulin light chain-associated Fanconi syndrome (disorder)", "Acquired monoclonal immunoglobulin light chain-associated Fanconi syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired monoclonal Ig light chain-associated Fanconi syndrome", "shortest_name_length": 60}
{"curie": "MONDO:0010328", "names": ["ATMDS", "acquired HbH disease", "Acquired HbH disease", "Acquired hemoglobin H disease", "acquired hemoglobin H disease", "Hemoglobin H Disease, Acquired", "Hemoglobin H disease, acquired", "Acquired haemoglobin H disease", "HEMOGLOBIN H DISEASE, ACQUIRED", "Acquired hemoglobin H disease (disorder)", "ALPHA-THALASSEMIA MYELODYSPLASIA SYNDROME", "ALPHA-thalassemia myelodysplasia syndrome", "alpha-thalassemia myelodysplasia syndrome", "Alpha-Thalassemia Myelodysplasia Syndrome", "Alpha-thalassemia-myelodysplastic syndrome", "alpha-thalassemia-myelodysplastic syndrome", "alpha-thalassemia myelodysplasia syndrome, somatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alpha-thalassemia-myelodysplastic syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C4053961", "names": ["SYRINGOMYELIA/HYDROMYELIA", "Syringomyelia and Hydromyelia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Syringomyelia and Hydromyelia", "shortest_name_length": 25}
{"curie": "MONDO:0014726", "names": ["CMT2X", "ARCMT2X", "SPG11 Charcot-Marie-Tooth disease", "Charcot-Marie-Tooth neuropathy type 2X", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2X", "Charcot-Marie-Tooth neuropathy, type 2X", "Charcot-Marie-Tooth disease axonal type 2X", "Charcot-Marie-Tooth disease, axonal, type 2x", "Charcot-Marie-Tooth disease, axonal, type 2X", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2X", "Autosomal recessive Charcot Marie Tooth disease type 2X", "Charcot-Marie-Tooth disease caused by mutation in SPG11", "autosomal recessive Charcot Marie Tooth disease type 2X", "Autosomal recessive Charcot-Marie-Tooth disease type 2X", "autosomal recessive Charcot-Marie-Tooth disease type 2X", "autosomal recessive axonal Charcot-Marie-Tooth disease type 2X", "Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2X", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2X", "Autosomal recessive Charcot-Marie-Tooth disease type 2X (disorder)", "autosomal recessive Charcot-Marie-Tooth disease type 2X (diagnosis)", "autosomal recessive Charcot-Marie-Tooth disease type 2 due to SPG11 mutation", "Autosomal recessive Charcot-Marie-Tooth disease type 2 due to SPG11 mutation", "Autosomal recessive Charcot-Marie-Tooth disease type 2 due to SPG11 (SPG11 vesicle trafficking associated, spatacsin) mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease axonal type 2X", "shortest_name_length": 5}
{"curie": "UMLS:C3642255", "names": ["Low Grade Ovarian Serous Adenocarcinoma", "Low-Grade Ovarian Serous Adenocarcinoma", "Ovarian Low-Grade Serous Adenocarcinoma", "ovarian adenocarcinoma serous low grade", "Ovarian Low Grade Serous Adenocarcinoma", "low grade serous adenocarcinoma of ovary", "Invasive Ovarian Micropapillary Serous Carcinoma", "low grade serous adenocarcinoma of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "low grade serous adenocarcinoma of ovary", "shortest_name_length": 39}
{"curie": "UMLS:C0575805", "names": ["hand swell", "hands swell", "Swollen hand", "hands swelled", "Hand swelling", "Swollen hands", "HAND SWELLING", "hand swelling", "hand; swelling", "swelling; hand", "Swelling of hand", "swelling of hand", "swelling of hands", "Swelling of hands", "Swelling of the hands", "Swelling of hand (finding)", "swelling of hand (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Swelling of hand", "shortest_name_length": 10}
{"curie": "MONDO:0002792", "names": ["vermis medulloblastoma", "Vermis Medulloblastoma", "cerebellar vermis medulloblastoma", "Cerebellar Vermis Medulloblastoma", "medulloblastoma of cerebellar vermis", "Medulloblastoma of Cerebellar Vermis", "medulloblastoma of the cerebellar vermis", "Medulloblastoma of the Cerebellar Vermis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellar vermis medulloblastoma", "shortest_name_length": 22}
{"curie": "MONDO:0014572", "names": ["LIKNS", "SCAR19", "LICHTENSTEIN-KNORR SYNDROME", "Lichtenstein-Knorr syndrome", "Lichtenstein Knorr syndrome", "autosomal recessive spinocerebellar ataxia 19", "spinocerebellar ataxia, autosomal recessive 19", "SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 19", "autosomal recessive spinocerebellar ataxia type 19", "SCAR19 - spinocerebellar ataxia, autosomal recessive 19", "Progressive autosomal recessive ataxia-deafness syndrome", "progressive autosomal recessive ataxia-deafness syndrome", "Progressive autosomal recessive ataxia, deafness syndrome", "Progressive autosomal recessive ataxia-sensorineural hearing loss syndrome", "progressive autosomal recessive ataxia-sensorineural hearing loss syndrome", "Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome", "Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lichtenstein-Knorr syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0008107", "names": ["hereditary vertical nystagmus", "Hereditary vertical nystagmus", "nystagmus, hereditary vertical", "Nystagmus, hereditary vertical", "NYSTAGMUS, HEREDITARY VERTICAL", "congenital hereditary vertical nystagmus", "Congenital hereditary vertical nystagmus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nystagmus, hereditary vertical", "shortest_name_length": 29}
{"curie": "MONDO:0013961", "names": ["HH16", "SEMA3A hypogonadotropic hypogonadism", "HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA", "hypogonadotropic hypogonadism 16 with or without anosmia", "hypogonadotropic hypogonadism caused by mutation in SEMA3A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadotropic hypogonadism 16 with or without anosmia", "shortest_name_length": 4}
{"curie": "UMLS:C0687148", "names": ["Mineral deficiency", "mineral deficiency", "Mineral Deficiency", "deficiency mineral", "deficiency minerals", "mineral; deficiency", "deficiency; mineral", "deficiencies mineral", "Mineral deficiency NOS", "Mineral deficiency (disorder)", "mineral deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mineral deficiency", "shortest_name_length": 18}
{"curie": "MONDO:0014725", "names": ["SPATCCM", "ASCT1 deficiency", "SPASTIC TETRAPLEGIA, THIN CORPUS CALLOSUM, AND PROGRESSIVE MICROCEPHALY", "spastic tetraplegia, thin corpus callosum, and progressive microcephaly", "Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome", "spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome", "spastic quadriplegia-thin corpus callosum-progressive postnatal microcephaly syndrome", "Spastic quadriplegia-thin corpus callosum-progressive postnatal microcephaly syndrome", "Spastic tetraplegia, thin corpus callosum, progressive postnatal microcephaly syndrome", "Spastic quadriplegia, thin corpus callosum, progressive postnatal microcephaly syndrome", "Spastic tetraplegia, thin corpus callosum, progressive postnatal microcephaly syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome", "shortest_name_length": 7}
{"curie": "MONDO:0032839", "names": ["NS12", "Noonan Syndrome 12", "noonan syndrome 12", "Noonan syndrome 12", "NOONAN SYNDROME 12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "noonan syndrome 12", "shortest_name_length": 4}
{"curie": "MONDO:0032882", "names": ["HESJAS", "HEYN-SPROUL-JACKSON SYNDROME", "Heyn-Sproul-Jackson syndrome", "MICROCEPHALY, SHORT STATURE, AND IMPAIRED INTELLECTUAL DEVELOPMENT", "Microcephaly, Short Stature, and Impaired Intellectual Development"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Heyn-Sproul-Jackson syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0000397", "names": ["ACP", "ataxic cerebral palsy", "ATAXIC CEREBRAL PALSY", "Ataxic cerebral palsy", "cerebral palsy ataxic", "Ataxic Cerebral Palsy", "hypotonic cerebral palsy", "cerebral; paralysis, ataxic", "cerebral; paralysis, ataxia", "paralysis; cerebral, ataxic", "Ataxic infantile cerebral palsy", "Ataxic cerebral palsy (disorder)", "ataxic cerebral palsy (diagnosis)", "Cerebral palsy, congenital, with ataxia", "CEREBRAL PALSY, ATAXIC, AUTOSOMAL RECESSIVE", "Cerebral Palsy, Ataxic, Autosomal Recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ataxic cerebral palsy", "shortest_name_length": 3}
{"curie": "EFO:0009963", "names": ["bipolar I disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bipolar I disorder", "shortest_name_length": 18}
{"curie": "UMLS:C3203533", "names": ["Psychological Trauma", "Psychological trauma", "psychological trauma", "Trauma, Psychological", "psychological trauma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Psychological Trauma", "shortest_name_length": 20}
{"curie": "MONDO:0001234", "names": ["Adhesive otitis", "adhesive otitis", "otitis; adhesive", "adhesive; otitis", "Middle ear adhesions", "adhesive otitis media", "Adhesive otitis media", "Adhesive otitis media, NOS", "adhesive otitis (diagnosis)", "Adhesive middle ear disease", "adhesive middle ear disease", "otitis media chronic adhesive", "chronic adhesive otitis media", "Chronic adhesive otitis media", "middle ear; disorder, adhesive", "Fibrotic adhesive otitis media", "Otitis media, chronic adhesive", "fibrotic adhesive otitis media", "Adhesive middle ear disease, NOS", "Adhesive middle ear disease (disorder)", "Chronic adhesive otitis media (diagnosis)", "disease (or disorder); middle ear, adhesive", "Adhesive middle ear disease, unspecified as to involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adhesive otitis media", "shortest_name_length": 15}
{"curie": "UMLS:C4525257", "names": ["Intrahepatic Bile Duct Cancer by AJCC v8 Stage", "Intrahepatic Bile Duct Carcinoma by AJCC v8 Stage", "Intrahepatic Bile Duct Cancer Tumor Stage (Pathologic)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intrahepatic Bile Duct Cancer by AJCC v8 Stage", "shortest_name_length": 46}
{"curie": "MONDO:0004380", "names": ["dendritic cell sarcoma", "Dendritic cell sarcoma", "sarcoma of dendritic cell", "Sarcoma of dendritic cells", "Dendritic Cell Sarcoma, NOS", "Dendritic cell sarcoma (disorder)", "follicular dendritic cell sarcoma", "sarcoma of dendritic cell (diagnosis)", "Sarcoma of dendritic cells (accessory cells)", "Dendritic Cell Tumor, Not Otherwise Specified", "Dendritic cell sarcoma not otherwise specified", "Dendritic cell sarcoma, not otherwise specified", "Dendritic cell sarcoma (morphologic abnormality)", "Dendritic cell sarcoma, not otherwise specified (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dendritic cell sarcoma", "shortest_name_length": 22}
{"curie": "MONDO:0012691", "names": ["LPRD2", "leopard syndrome 2", "LEOPARD syndrome 2", "LEOPARD SYNDROME 2", "Leopard Syndrome 2", "LEOPARD syndrome, 2", "Leopard syndrome type 2", "Noonan syndrome with multiple lentigines 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "LEOPARD syndrome 2", "shortest_name_length": 5}
{"curie": "MONDO:0010552", "names": ["Charcot Marie Tooth type 1 aplasia cutis congenita", "CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED, WITH APLASIA CUTIS CONGENITA", "Charcot-Marie-Tooth peroneal muscular atrophy, X-linked, with aplasia cutis congenita"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth peroneal muscular atrophy, X-linked, with aplasia cutis congenita", "shortest_name_length": 50}
{"curie": "UMLS:C4688320", "names": ["Refractory Gastric Carcinoma", "Refractory Gastric (Stomach) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Gastric Carcinoma", "shortest_name_length": 28}
{"curie": "MONDO:0000411", "names": ["electroclinical syndrome", "electro-clinical syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "electroclinical syndrome", "shortest_name_length": 24}
{"curie": "MONDO:0009119", "names": ["diverticulosis, small-intestinal", "Diverticulosis, Small Intestinal", "DIVERTICULOSIS, SMALL-INTESTINAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diverticulosis, small-intestinal", "shortest_name_length": 32}
{"curie": "MONDO:0009527", "names": ["LPL AND HL DEFICIENCY", "Lpl And Hl Deficiency", "LPL and HL deficiency", "Lpl And Htgl Deficiency", "LPL and HTGL deficiency", "LPL AND HTGL DEFICIENCY", "familial LMF1 deficiency", "Familial LMF1 deficiency", "lipase deficiency combined", "combined lipase deficiency", "Lipase deficiency combined", "Combined Lipase Deficiency", "Lipase Deficiency, Combined", "LIPASE DEFICIENCY, COMBINED", "lipase deficiency, combined", "familial lipase maturation factor 1 deficiency", "Familial lipase maturation factor 1 deficiency", "lipoprotein lipase deficiency with hepatic triglyceride lipase deficiency", "Lipoprotein lipase deficiency with hepatic triglyceride lipase deficiency", "LIPOPROTEIN LIPASE DEFICIENCY WITH HEPATIC TRIGLYCERIDE LIPASE DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lipase deficiency, combined", "shortest_name_length": 21}
{"curie": "MONDO:0032918", "names": ["DEE84", "EIEE84", "Jamuar Syndrome", "Jamuar syndrome", "JAMUAR SYNDROME", "early infantile epileptic encephalopathy 84", "EPILEPTIC ENCEPHALOPATHY, EARLY IFANTILE, 84", "epileptic encephalopathy, early infantile, 84", "developmental and epileptic encephalopathy 84", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 84", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 84", "developmental and epileptic encephalopathy, 84"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 84", "shortest_name_length": 5}
{"curie": "UMLS:C3829184", "names": ["Stage IVa", "Masaoka Stage IVa", "Masaoka-Koga Stage IVa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Masaoka-Koga Stage IVa", "shortest_name_length": 9}
{"curie": "MONDO:0008571", "names": ["Blount disease", "Tibia vara Blount", "Infantile tibia vara", "TIBIA VARA, INFANTILE", "tibia vara, infantile", "Blount disease (disorder)", "BLOUNT DISEASE, INFANTILE", "Blount disease, infantile", "Osteochondrosis deformans tibiae", "OSTEOCHONDROSIS DEFORMANS TIBIAE, INFANTILE", "Osteochondrosis deformans tibiae, infantile", "Osteochondrosis deformans tibiae-familial infantile type", "OSTEOCHONDROSIS DEFORMANS TIBIAE, FAMILIAL INFANTILE TYPE", "Osteochondrosis deformans tibiae, familial infantile type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Blount disease, infantile", "shortest_name_length": 14}
{"curie": "MONDO:0010296", "names": ["XLA2", "IMD61", "AGMX2", "immunodeficiency 61", "IMMUNODEFICIENCY 61", "agammaglobulinemia X-linked type 2", "AGAMMAGLOBULINEMIA, X-LINKED, TYPE 2", "Agammaglobulinemia, X-linked, type 2", "agammaglobulinemia, X-linked, type 2", "immunodeficiency 61, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 61", "shortest_name_length": 4}
{"curie": "MONDO:0001460", "names": ["Dyshormogenetic goiter", "Dyshormonogenic goiter", "dyshormonogenic goiter", "Dyshormonogenic goitre", "dyshormonogenic goitre", "Dyshormogenetic goitre", "dyshormogenetic; goiter", "struma; dyshormogenetic", "Dyshormonogenic goiter (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyshormonogenic goiter", "shortest_name_length": 22}
{"curie": "MONDO:0024522", "names": ["PCA", "PCA1", "PLCA1", "amyloidosis 9", "amyloidosis IX", "Amyloidosis IX", "AMYLOIDOSIS IX", "Familial amyloidosis cutis", "Familial lichen amyloidosis", "lichen amyloidosis, familial", "LICHEN AMYLOIDOSIS, FAMILIAL", "Lichen Amyloidosis, Familial", "amyloidosis, primary cutaneous, 1", "AMYLOIDOSIS, PRIMARY CUTANEOUS, 1", "OSMR primary cutaneous amyloidosis", "AMYLOIDOSIS, FAMILIAL CUTANEOUS LICHEN", "Cutaneous lichen amyloidosis, familial", "Lichen Amyloidosis, Familial Cutaneous", "Familial lichen amyloidosis (disorder)", "amyloidosis, familial cutaneous lichen", "Amyloidosis, Familial Cutaneous Lichen", "primary localized cutaneous amyloidosis 1", "amyloidosis, primary localized cutaneous, 1", "AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 1", "Dominant primary localised cutaneous amyloidosis", "amyloidosis, primary localized cutaneous, type 1", "Dominant primary localized cutaneous amyloidosis", "Familial generalised dyschromic amyloidosis cutis", "Familial generalized dyschromic amyloidosis cutis", "Familial Primary Localized Cutaneous Amyloidosis-1", "familial primary localized cutaneous amyloidosis-1", "primary cutaneous amyloidosis caused by mutation in OSMR", "Dominant primary localized cutaneous amyloidosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyloidosis, primary localized cutaneous, 1", "shortest_name_length": 3}
{"curie": "MONDO:0001756", "names": ["frontal sinus cancer", "cancer of frontal sinus", "Malignant Frontal Sinus Tumor", "malignant frontal sinus tumor", "Malignant tumor of frontal sinus", "malignant tumor of frontal sinus", "malignant frontal sinus neoplasm", "Malignant Tumor of Frontal Sinus", "Malignant Frontal Sinus Neoplasm", "Malignant tumour of frontal sinus", "Malignant Neoplasm of Frontal Sinus", "malignant neoplasm of frontal sinus", "Malignant neoplasm of frontal sinus", "malignant tumor of the Frontal sinus", "Malignant Tumor of the Frontal Sinus", "malignant tumor of the frontal sinus", "malignant neoplasm of the frontal sinus", "Malignant Neoplasm of the Frontal Sinus", "Malignant tumor of frontal sinus (disorder)", "malignant neoplasm of frontal sinus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontal sinus cancer", "shortest_name_length": 20}
{"curie": "UMLS:C1335472", "names": ["Premalignant", "Premalignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Premalignant Neoplasm", "shortest_name_length": 12}
{"curie": "UMLS:C1334786", "names": ["Teratoid Hepatoblastoma", "Mixed Hepatoblastoma with Teratoid Features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Teratoid Hepatoblastoma", "shortest_name_length": 23}
{"curie": "UMLS:C4330727", "names": ["Myeloid Neoplasms with Germline Predisposition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myeloid Neoplasms with Germline Predisposition", "shortest_name_length": 46}
{"curie": "UMLS:C0272693", "names": ["open fracture of neck of metacarpal bone", "Open Fracture of Neck of Metacarpal Bone", "Open fracture of neck of metacarpal bone", "Open fracture of neck of metacarpal bones", "Open fracture of neck of metacarpal bone(s)", "Open fracture of neck of metacarpal bone (disorder)", "open fracture of neck of metacarpal bone (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Open fracture of neck of metacarpal bone", "shortest_name_length": 40}
{"curie": "MONDO:0020754", "names": ["VSCM", "VSCM1", "VISCERAL MYOPATHY", "Visceral Myopathy", "visceral myopathy", "Myopathy, Visceral", "VISCERAL MYOPATHY 1", "Visceral Myopathies", "visceral myopathy 1", "infantile visceral myopathy", "megaduodenum and/or megacystis", "pseudoobstruction, idiopathic intestinal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "visceral myopathy 1", "shortest_name_length": 4}
{"curie": "MONDO:0017201", "names": ["Spasmus Nutans", "spasmus nutans", "Spasmus nutans", "Spasmus nutans (disease)", "Spasmus nutans (disorder)", "Spasmus nutans (diagnosis)", "nystagmus acquired spasmus nutans"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spasmus nutans", "shortest_name_length": 14}
{"curie": "MONDO:0017921", "names": ["Tungland-Bellman syndrome", "Tungland Bellman syndrome", "Tunglang Savage Bellman syndrome", "Tunglang savage Bellman syndrome", "Hearing loss insensitivity to aldosterone", "hearing loss insensitivity to aldosterone", "hearing loss and familial salivary gland insensitivity to aldosterone", "Hearing loss and salivary gland insensitivity to aldosterone syndrome", "Hearing loss and familial salivary gland insensitivity to aldosterone", "Hearing loss-familial salivary gland insensitivity to aldosterone syndrome", "hearing loss-familial salivary gland insensitivity to aldosterone syndrome", "Hearing loss and salivary gland insensitivity to aldosterone syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss-familial salivary gland insensitivity to aldosterone syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0019932", "names": ["Vagina absent", "Absent vagina", "vagina absence", "vagina; absent", "Vagina aplasia", "Vaginal atresia", "atresia vaginal", "VAGINAL ABSENCE", "absence; vagina", "Vaginal Atresia", "vaginal atresia", "atresia; vagina", "vagina; atresia", "vagina agenesis", "Vaginal agenesis", "agenesis; vagina", "vagina; agenesis", "Atresia of vagina", "Absence of vagina", "absence of vagina", "atresia of vagina", "Agenesis of vagina", "agenesis of vagina", "Vagina, absence of", "Aplasia of the vagina", "the vagina was absent", "Vagina absent (finding)", "VAGINA CONGENITAL ABSENCE", "vaginal atresia (diagnosis)", "Congenital absence of vagina", "congenital absence of vagina", "vaginal atresia was observed", "Congenital agenesis of vagina", "agenesis of vagina (diagnosis)", "Congenital absence of the vagina", "isolated partial vaginal agenesis", "Isolated partial vaginal agenesis", "Abnormally closed or absent vagina", "absence of vagina (physical finding)", "atresia of vagina (physical finding)", "vagina noninflammatory disorder atresia", "Congenital absence of vagina (disorder)", "Congenital agenesis of vagina (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated partial vaginal agenesis", "shortest_name_length": 13}
{"curie": "UMLS:C1515298", "names": ["Spermatocytic Tumor with Sarcoma", "Testicular Spermatocytic Tumor with Sarcoma", "Testicular Spermatocytic Seminoma with Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular Spermatocytic Tumor with Sarcoma", "shortest_name_length": 32}
{"curie": "MONDO:0006271", "names": ["LGCOS", "low grade central osteosarcoma", "Low grade central osteosarcoma", "low-grade central osteosarcoma", "Low-grade central osteosarcoma", "Low Grade Central Osteosarcoma", "Intraosseous low grade osteosarcoma", "Low Grade Intramedullary Osteosarcoma", "low-grade intramedullary osteosarcoma", "Low-grade intramedullary osteosarcoma", "low grade intramedullary osteosarcoma", "Low-Grade Intramedullary Osteosarcoma", "intraosseous well-differentiated osteosarcoma", "Intraosseous Well-Differentiated Osteosarcoma", "Intraosseous well differentiated osteosarcoma", "intraosseous well-differentiated osteogenic sarcoma", "Intraosseous Well-Differentiated Osteogenic Sarcoma", "Low grade central osteosarcoma (morphologic abnormality)", "Intraosseous well differentiated osteosarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "low grade central osteosarcoma", "shortest_name_length": 5}
{"curie": "UMLS:C4684941", "names": ["Refractory Lymphocyte-Rich Classic Hodgkin Lymphoma", "Refractory Lymphocyte-Rich Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Lymphocyte-Rich Classic Hodgkin Lymphoma", "shortest_name_length": 51}
{"curie": "MONDO:0019582", "names": ["self-healing papular mucinosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "self-healing papular mucinosis", "shortest_name_length": 30}
{"curie": "MONDO:0008526", "names": ["TALONAVICULAR COALITION", "talonavicular coalition", "Talonavicular coalition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "talonavicular coalition", "shortest_name_length": 23}
{"curie": "MONDO:0032858", "names": ["DEE81", "EIEE81", "early infantile epileptic encephalopathy 81", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 81", "epileptic encephalopathy, early infantile, 81", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 81", "developmental and epileptic encephalopathy 81", "developmental and epileptic encephalopathy, 81"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 81", "shortest_name_length": 5}
{"curie": "MONDO:0007747", "names": ["HYCHL", "Isolated hyperchlorhidrosis", "isolated hyperchlorhidrosis", "HYPERCHLORHIDROSIS, ISOLATED", "hyperchlorhidrosis, isolated", "Carbonic anhydrase XII deficiency", "carbonic anhydrase XII deficiency", "Isolated hyperchlorhidrosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated hyperchlorhidrosis", "shortest_name_length": 5}
{"curie": "UMLS:C4725790", "names": ["Refractory T Acute Lymphoblastic Leukemia", "Refractory T-Acute Lymphoblastic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory T Acute Lymphoblastic Leukemia", "shortest_name_length": 41}
{"curie": "UMLS:C0859078", "names": ["Maternal drugs affecting fetus", "Maternal drugs affecting foetus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Maternal drugs affecting fetus", "shortest_name_length": 30}
{"curie": "MONDO:0012023", "names": ["DFNA49", "autosomal dominant deafness 49", "deafness, autosomal dominant 49", "Deafness, Autosomal Dominant 49", "DEAFNESS, AUTOSOMAL DOMINANT 49", "autosomal dominant nonsyndromic deafness 49", "autosomal dominant nonsyndromic hearing loss 49", "autosomal dominant nonsyndromic deafness type 49"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 49", "shortest_name_length": 6}
{"curie": "MONDO:0013079", "names": ["PBC2", "primary biliary cholangitis 2", "BILIARY CIRRHOSIS, PRIMARY, 2", "biliary cirrhosis, primary, 2", "Biliary Cirrhosis, Primary, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary biliary cholangitis 2", "shortest_name_length": 4}
{"curie": "UMLS:C4329303", "names": ["Anemia due to Decreased Production"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anemia due to Decreased Production", "shortest_name_length": 34}
{"curie": "UMLS:C4763439", "names": ["Spastic Paraplegia 76"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spastic Paraplegia 76", "shortest_name_length": 21}
{"curie": "MONDO:0018588", "names": ["LECT2 amyloidosis", "ALECT2 amyloidosis", "leukocyte chemotactic factor-2 amyloidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ALECT2 amyloidosis", "shortest_name_length": 17}
{"curie": "MONDO:0009797", "names": ["OAWA", "UMPS", "oroticaciduria", "Oroticaciduria", "orotic aciduria", "UMPS DEFICIENCY", "Orotic aciduria", "OROTIC ACIDURIA", "Umps deficiency", "orotic; aciduria", "oroticaciduria 1", "acidurias orotic", "Oroticaciduria 1", "aciduria; orotic", "OROTIC ACIDURIA I", "orotic aciduria 1", "Orotic aciduria, NOS", "orotic aciduria type 1", "Ump synthase deficiency", "UMP SYNTHASE DEFICIENCY", "UMP synthase deficiency", "OPRT and ODC deficiency", "OPRT AND ODC DEFICIENCY", "UMP synthtase deficiency", "Hereditary orotic aciduria", "Hereditary Orotic Aciduria", "Orotic aciduria (disorder)", "hereditary orotic aciduria", "orotic aciduria (diagnosis)", "Orotic aciduria, hereditary", "OROTIC ACIDURIA, HEREDITARY", "orotic aciduria II (formerly)", "High urine orotic acid levels", "Hereditary orotic aciduria, NOS", "Hereditary orotic aciduria type 1", "Hereditary orotic aciduria, type 1", "orotidylic decarboxylase deficiency", "Orotidylic decarboxylase deficiency", "OPRT and OMP decarboxylase deficiency", "OPRT AND OMP decarboxylase deficiency", "Hereditary orotic aciduria (disorder)", "URIDINE MONOPHOSPHATE SYNTHASE DEFICIENCY", "Uridine monophosphate synthase deficiency", "uridine monophosphate synthase deficiency", "Increased urinary orotic acid concentration", "uridine monophosphate synthetase deficiency", "Uridine monophosphate synthetase deficiency", "Deficiency of orotidylic acid phosphorylase", "orotic aciduria without megaloblastic Anemia", "OROTIC ACIDURIA WITHOUT MEGALOBLASTIC ANEMIA", "orotate phosphoribosyltransferase deficiency", "Hereditary orotic aciduria, type 1 (disorder)", "Deficiency of orotate phosphoribosyltransferase", "UMPS - Uridine monophosphate synthase deficiency", "Deficiency of orotate phosphoribosyltransferase (disorder)", "Orotidylic pyrophosphorylase orotidylic decarboxylase deficiency", "Orotate phosphoribosyltransferase and omp decarboxylase deficiency", "orotate phosphoribosyltransferase and OMP decarboxylase deficiency", "OROTIDYLIC PYROPHOSPHORYLASE AND OROTIDYLIC DECARBOXYLASE DEFICIENCY", "orotidylic pyrophosphorylase and orotidylic decarboxylase deficiency", "Orotidylic pyrophosphorylase and orotidylic decarboxylase deficiency", "OROTATE PHOSPHORIBOSYLTRANSFERASE AND OROTIDYLIC DECARBOXYLASE DEFICIENCY", "orotate phosphoribosyltransferase and orotidylic decarboxylase deficiency", "Combined orotic acid phosphoribosyltransferase and orotidine - 5 - phosphate decarboxylase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orotic aciduria", "shortest_name_length": 4}
{"curie": "MONDO:0017454", "names": ["TPT-PS syndrome", "triphalangeal thumb-polysyndactyly syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "triphalangeal thumb-polysyndactyly syndrome", "shortest_name_length": 15}
{"curie": "UMLS:C5419565", "names": ["Refractory Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma", "shortest_name_length": 66}
{"curie": "MONDO:0800109", "names": ["PTI", "persistent tachypnoe of infancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "persistent tachypnoe of infancy", "shortest_name_length": 3}
{"curie": "MONDO:0003942", "names": ["eosinophilic variant of chromophobe renal cell carcinoma", "Eosinophilic Variant of Chromophobe Renal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eosinophilic variant of chromophobe renal cell carcinoma", "shortest_name_length": 56}
{"curie": "OMIM:111200", "names": [], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"]}
{"curie": "MONDO:0013705", "names": ["MRT19", "mental retardation, autosomal recessive 19", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 19", "intellectual disability, autosomal recessive 19", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 19"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 19", "shortest_name_length": 5}
{"curie": "UMLS:C0280385", "names": ["nasopharynx lymphoepithelioma, stage IV", "Nasopharyngeal lymphepithelioma stage IV", "Stage IV Nasopharyngeal Lymphoepithelioma", "nasopharynx lymphoepithelioma, metastatic", "Stage IV Lymphoepithelioma of Nasopharynx", "Nasopharyngeal lymphoepithelioma stage IV", "nasopharyngeal lymphoepithelioma, stage IV", "nasopharyngeal lymphoepithelioma, metastatic", "stage IV lymphoepithelioma of the nasopharynx", "Stage IV Lymphoepithelioma of the Nasopharynx", "lymphoepithelioma of the nasopharynx, stage IV", "metastatic lymphoepithelioma of the nasopharynx", "lymphoepithelioma of the nasopharynx, metastatic", "Stage IV Nasopharyngeal Undifferentiated Carcinoma", "Nasopharyngeal Undifferentiated Carcinoma Stage IV", "Stage IV Undifferentiated Nasopharyngeal Throat Cancer", "Stage IV Nasopharyngeal Undifferentiated Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasopharyngeal lymphoepithelioma stage IV", "shortest_name_length": 39}
{"curie": "UMLS:C0279586", "names": ["non-T, non-B, cALLa positive childhood ALL", "pediatric ALL, non-T, non-B, cALLa positive", "childhood ALL, non T, non B, cALLa positive", "childhood ALL, non-T, non-B, cALLa positive", "cALLa positive, non T, non B, childhood ALL", "cALLa positive, non-T, non-B, childhood ALL", "pediatric ALL, non T, non B, cALLa positive", "ALL, cALLa positive, non-T, non-B, pediatric", "ALL, childhood, non T, non B, cALLa positive", "ALL, pediatric, non T, non B, cALLa positive", "ALL, childhood, non-T, non-B, cALLa positive", "ALL, non T, non B, cALLa positive, childhood", "ALL, pediatric, non-T, non-B, cALLa positive", "ALL, non-T, non-B, cALLa positive, childhood", "leukemia, pediatric ALL non-T, non-B, cALLa positive", "leukemia, childhood ALL non-T, non-B, cALLa positive", "leukemia, ALL non T, non B, cALLa positive, childhood", "leukemia, ALL non-T, non-B, cALLa positive, childhood", "Non-T Non-B CALLA Positive Acute Lymphoblastic Leukemia", "non-B, non-T, cALLa positive childhood acute lymphocytic leukemia", "non-T, non-B, cALLa positive childhood acute lymphocytic leukemia", "Non-T Non-B CALLA Positive Childhood Acute Lymphoblastic Leukemia", "non B, non T, cALLa positive childhood acute lymphocytic leukemia", "non T, non B, cALLa positive childhood acute lymphocytic leukemia", "leukemia, childhood acute lymphocytic non-T, non-B, cALLa positive", "acute lymphocytic leukemia, childhood non-T, non-B, cALLa positive", "leukemia, pediatric acute lymphocytic non-T, non-B, cALLa positive", "non-T, non-B, cALLa positive childhood acute lymphoblastic leukemia", "acute lymphoblastic leukemia, childhood non-T, non-B, cALLa positive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-T Non-B CALLA Positive Childhood Acute Lymphoblastic Leukemia", "shortest_name_length": 42}
{"curie": "UMLS:C0272271", "names": ["liver disease; coagulation defect", "coagulation defect; liver disease", "Coagulation Defects due to Liver Disease", "Coagulation defects due to liver disease", "Blood coagulation disorder due to liver disease", "Blood Coagulation Disorder due to Liver Disease", "Coagulation Disorder Related to Liver Dysfunction", "Blood coagulation disorder due to liver disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Blood coagulation disorder due to liver disease", "shortest_name_length": 33}
{"curie": "MONDO:0004357", "names": ["supraglottic cancer", "Supraglottic Cancer", "Cancer of Supraglottis", "supraglottic carcinoma", "Supraglottic carcinoma", "cancer of supraglottis", "Supraglottic Carcinoma", "Supraglottis Carcinoma", "supraglottis carcinoma", "carcinoma of supraglottis", "Carcinoma of supraglottis", "Carcinoma of Supraglottis", "Supraglottic Throat Cancer", "cancer of the supraglottis", "Cancer of the Supraglottis", "supraglottic throat cancer", "carcinoma of the supraglottis", "Carcinoma of the Supraglottis", "Carcinoma of supraglottis (disorder)", "Carcinoma of supraglottis (diagnosis)", "supraglottic part of larynx carcinoma", "carcinoma of supraglottic part of larynx", "malignant neoplasm of supraglottis carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma of supraglottis", "shortest_name_length": 19}
{"curie": "UMLS:C1709361", "names": ["Outer Hair Sheath and Infundibulum Tumor", "Outer Hair Sheath and Infundibulum Neoplasm", "Tumor of the Outer Hair Sheath and Infundibulum", "Neoplasm of the Outer Hair Sheath and Infundibulum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Outer Hair Sheath and Infundibulum Neoplasm", "shortest_name_length": 40}
{"curie": "MONDO:0012873", "names": ["SCDEDS", "EDSSPD3", "SCD-EDS", "spEDS-SLC39A13", "SLC39A13-related spEDS", "EDS, spondylocheirodysplastic type", "SLC39A13-related spondylodysplastic EDS", "Spondylocheirodysplastic Ehlers-Danlos syndrome", "Ehlers-Danlos syndrome spondylodysplastic type 3", "EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 3", "Ehlers-Danlos syndrome, spondylodysplastic type, 3", "spondylocheirodysplasia, Ehlers-Danlos syndrome-like", "SPONDYLOCHEIRODYSPLASIA, EHLERS-DANLOS SYNDROME-LIKE", "Spondylocheirodysplasia, Ehlers-Danlos Syndrome-Like", "Ehlers-Danlos syndrome spondylocheirodysplastic type", "Ehlers-Danlos syndrome, spondylocheirodysplastic type", "SLC39A13-related spondylodysplastic Ehlers-Danlos syndrome", "Ehlers-Danlos syndrome spondylocheirodysplastic type (disorder)", "Ehlers-Danlos syndrome spondylocheirodysplastic type (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ehlers-Danlos syndrome, spondylocheirodysplastic type", "shortest_name_length": 6}
{"curie": "MONDO:0019943", "names": ["continuous muscle fiber activity hereditary", "Hereditary continuous muscle fibre activity", "Hereditary continuous muscle fiber activity", "hereditary continuous muscle fiber activity", "CONTINUOUS MUSCLE FIBER ACTIVITY, HEREDITARY", "Continuous Muscle Fiber Activity, Hereditary", "Hereditary continuous muscle fiber activity (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary continuous muscle fiber activity", "shortest_name_length": 43}
{"curie": "UMLS:C4725841", "names": ["Muscle-Invasive Bladder Carcinoma", "Muscle Invasive Bladder Carcinoma", "Bladder Carcinoma Infiltrating the Muscle of the Bladder Wall"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Muscle Invasive Bladder Carcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C4085325", "names": ["Evagination", "EVAGINATION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Evagination", "shortest_name_length": 11}
{"curie": "UMLS:C2919207", "names": ["Acoustic Nerve Palsy", "Cranial nerve palsy VIII", "Cranial Nerve VIII Palsy", "Eight Cranial Nerve Palsy", "Eighth cranial nerve palsy", "Vestibulocochlear nerve palsy", "Vestibulocochlear Nerve Palsy", "Vestibulocochlear nerve palsy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vestibulocochlear nerve palsy", "shortest_name_length": 20}
{"curie": "MONDO:0004180", "names": ["urologic neoplasm", "Urologic Neoplasm", "Urologic Neoplasms", "Neoplasm, Urologic", "Neoplasms, Urologic", "urinary tract tumor", "Urological Neoplasm", "Neoplasm;urological", "Urinary Tract Tumor", "tract tumors urinary", "Urinary System Tumor", "Neoplasm, Urological", "Urological Neoplasms", "Neoplasms, Urological", "Tumor of Urinary Tract", "Urinary tract neoplasm", "tumor of urinary tract", "urinary tract neoplasm", "Tumor of urinary tract", "Urinary Tract Neoplasm", "Tumor of Urinary System", "Tract Neoplasm, Urinary", "Urinary Tract Neoplasms", "Tumour of urinary tract", "Urinary System Neoplasm", "Neoplasm, Urinary Tract", "urinary system neoplasm", "Urinary tract neoplasia", "Tract Neoplasms, Urinary", "Neoplasms, Urinary Tract", "Neoplasm of urinary tract", "Neoplasm of Urinary Tract", "Neoplasm of urinary system", "Tumor of the Urinary Tract", "Neoplasm of Urinary System", "neoplasm of urinary system", "Benign Urinary Tract Tumor", "benign urinary tract tumor", "Urinary tract neoplasm NOS", "Tumor of the Urinary System", "tumor of the urinary system", "renal system benign neoplasm", "Neoplasm of the Urinary Tract", "Benign urinary tract neoplasm", "benign tumor of urinary tract", "Benign tumor of urinary tract", "benign urinary tract neoplasm", "Benign Tumor of Urinary Tract", "Benign Urinary Tract Neoplasm", "Benign neoplasm urinary tract", "Neoplasm of the Urinary System", "Benign Urinary System Neoplasm", "benign urinary system neoplasm", "Urinary tract neoplasms benign", "urinary system benign neoplasm", "Benign tumour of urinary tract", "Benign Neoplasm of Urinary Tract", "Neoplasm of urinary tract proper", "Benign neoplasm of urinary tract", "benign neoplasm of urinary tract", "Benign urinary tract neoplasm NOS", "Benign neoplasm of urinary system", "Benign Tumor of the Urinary Tract", "benign tumor of the urinary tract", "benign neoplasm of urinary organs", "neoplasm of the urological system", "benign neoplasm of the urinary tract", "Benign Neoplasm of the Urinary Tract", "Neoplasm of urinary system (disorder)", "Benign neoplasm of urinary system NOS", "Benign neoplasm of urinary system, NOS", "Other unspecified neoplasm urinary tract", "Neoplasm of urinary tract proper (disorder)", "Benign neoplasm of urinary system (disorder)", "benign neoplasm of urinary organs (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign urinary system neoplasm", "shortest_name_length": 17}
{"curie": "MONDO:0018026", "names": ["Tetraploid", "Tetraploids", "Tetraploidy", "tetraploidy", "4n syndrome", "Tetraploidies", "92.XXYY syndrome", "92,XXXX syndrome", "tetraploidy syndrome", "Tetraploidy (disorder)", "chromosome tetraploidy syndrome", "Tetraploidy (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tetraploidy syndrome", "shortest_name_length": 10}
{"curie": "UMLS:C0278723", "names": ["stage II multiple myeloma", "Multiple Myeloma Stage II", "Stage II Multiple Myeloma", "multiple myeloma, stage II", "DS Stage II Multiple Myeloma", "Stage II Plasma Cell Myeloma", "plasma cell neoplasm, stage II", "DS Stage II Plasma Cell Myeloma", "Durie/Salmon Stage II Multiple Myeloma", "Durie/Salmon Stage II Plasma Cell Myeloma", "DS Stage II Multiple Myeloma/Plasma Cell Myeloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DS Stage II Plasma Cell Myeloma", "shortest_name_length": 25}
{"curie": "MONDO:0005532", "names": ["Crohn Colitis", "Crohn colitis", "Crohn's colitis", "Crohn's Colitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Crohn's colitis", "shortest_name_length": 13}
{"curie": "MONDO:0004341", "names": ["Pancreatic Colloid Carcinoma", "mucinous Noncystic carcinoma", "Mucinous Noncystic Carcinoma", "colloid carcinoma of the pancreas", "Colloid Carcinoma of the Pancreas", "pancreatic mucinous Noncystic carcinoma", "Pancreatic Mucinous Noncystic Carcinoma", "Colloid carcinoma (Mucinous noncystic carcinoma)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colloid carcinoma of the pancreas", "shortest_name_length": 28}
{"curie": "MONDO:0032770", "names": ["IDDSSAD", "ACTL6B-related BAFopathy", "INTELLECTUAL DEVELOPMENTAL DISORDER WITH SEVERE SPEECH AND AMBULATION DEFECTS", "intellectual developmental disorder with severe speech and ambulation defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder with severe speech and ambulation defects", "shortest_name_length": 7}
{"curie": "UMLS:C0149518", "names": ["Acute Gastritis", "Gastritis acute", "Gastritis;acute", "acute gastritis", "GASTRITIS ACUTE", "Acute gastritis", "gastritis acute", "acute; gastritis", "gastritis; acute", "GASTRITIS, ACUTE", "Acute gastritis (disorder)", "acute gastritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute gastritis", "shortest_name_length": 15}
{"curie": "MONDO:0015308", "names": ["laminopathy type Decaudain-Vigouroux", "Laminopathy type Decaudain Vigouroux", "Laminopathy type Decaudain Vigouroux (diagnosis)", "laminopathy with severe metabolic syndrome and myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laminopathy type Decaudain-Vigouroux", "shortest_name_length": 36}
{"curie": "MONDO:0005597", "names": ["cystic renal cell carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cystic renal cell carcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C4683692", "names": ["Enteropathy-Associated T-Cell Lymphoma by Ann Arbor Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Enteropathy-Associated T-Cell Lymphoma by Ann Arbor Stage", "shortest_name_length": 57}
{"curie": "UMLS:C4727781", "names": ["Locally Advanced Non-Squamous Non-Small Cell Lung Cancer", "Locally Advanced Non-Squamous Non-Small Cell Lung Carcinoma", "Locally Advanced Lung Non-Squamous Non-Small Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Lung Non-Squamous Non-Small Cell Carcinoma", "shortest_name_length": 56}
{"curie": "MONDO:0018470", "names": ["Renal aplasia", "renal aplasia", "Absent kidney", "Renal Agenesis", "RENAL AGENESIS", "renal agenesis", "agenesis renal", "Missing kidney", "Renal agenesis", "renal adysplasia", "agenesis; kidney", "kidney; agenesis", "absent/small kidney", "hereditary renal aplasia", "renal agenesis (disease)", "renal agenesis/hypoplasia", "absence congenital kidney", "congenital absence kidney", "Renal agenesis (disorder)", "Renal agenesis congenital", "renal hypodysplasia/aplasia", "kidney; absence, congenital", "Renal agenesis, unspecified", "absent/underdeveloped kidney", "Congenital absence of kidney", "congenital absence of kidney", "CONGENITAL ABSENCE OF KIDNEY", "Congenital absence of the kidney", "hereditary urogenital adysplasia", "congenital absence of kidney (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal agenesis", "shortest_name_length": 13}
{"curie": "MONDO:0014391", "names": ["IMD24", "IMMUNODEFICIENCY 24", "immunodeficiency 24", "immunodeficiency type 24", "SCID due to CTPS1 deficiency", "Severe combined immunodeficiency due to CTPS1 deficiency", "severe combined immunodeficiency due to CTPS1 deficiency", "Severe combined immunodeficiency due to cytidine 5-prime triphosphate synthetase 1 deficiency", "Severe combined immunodeficiency due to cytidine 5-prime triphosphate synthetase 1 deficiency (disorder)", "Severe combined immunodeficiency due to cytidine 5-prime triphosphate synthetase 1 deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe combined immunodeficiency due to CTPS1 deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0700128", "names": ["translocation Down syndrome", "Robertsonian Translocation Trisomy 21"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "translocation Down syndrome", "shortest_name_length": 27}
{"curie": "MONDO:0016917", "names": ["partial monosomy of chromosome 19q", "partial deletion of chromosome 19q", "partial monosomy of the long arm of chromosome 19", "partial deletion of the long arm of chromosome 19", "partial deletion of the long arm of chromosome type 19"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of the long arm of chromosome 19", "shortest_name_length": 34}
{"curie": "UMLS:C2349261", "names": ["Relapse multiple myeloma", "multiple myeloma in relapse", "Multiple myeloma in relapse", "Multiple myeloma, in relapse", "Relapse multiple myeloma (disorder)", "multiple myeloma in relapse (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Relapse multiple myeloma", "shortest_name_length": 24}
{"curie": "MONDO:0022843", "names": ["congenital mumps"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital mumps", "shortest_name_length": 16}
{"curie": "UMLS:C4725175", "names": ["Acute Submassive Pulmonary Embolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Submassive Pulmonary Embolism", "shortest_name_length": 35}
{"curie": "UMLS:C4524743", "names": ["Gastroesophageal Junction Adenocarcinoma by AJCC v8 ypTNM Stage", "Gastroesophageal Junction Adenocarcinoma by AJCC v8 Postneoadjuvant Therapy Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastroesophageal Junction Adenocarcinoma by AJCC v8 Postneoadjuvant Therapy Stage", "shortest_name_length": 63}
{"curie": "UMLS:C0862221", "names": ["Mycosis fungoides/Sezary syndrome stage III", "stage III mycosis fungoides/Sezary syndrome", "mycosis fungoides/Sezary syndrome, stage III", "stage III cutaneous T-cell non-Hodgkin lymphoma", "Stage III Mycosis Fungoides and Sezary Syndrome", "Stage III Mycosis Fungoides and Sézary Syndrome", "stage III mycosis fungoides and the Sezary syndrome", "Stage III Mycosis Fungoides and Sézary Syndrome AJCC v7", "Stage III Mycosis Fungoides and Sezary Syndrome AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Mycosis Fungoides and Sezary Syndrome AJCC v7", "shortest_name_length": 43}
{"curie": "MONDO:0007224", "names": ["brachydactyly, type E, with atrial septal defect, type 2", "Brachydactyly, Type E, with Atrial Septal Defect, Type II", "BRACHYDACTYLY, TYPE E, WITH ATRIAL SEPTAL DEFECT, TYPE II", "brachydactyly, type E, with atrial septal defect, type II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly, type E, with atrial septal defect, type 2", "shortest_name_length": 56}
{"curie": "MONDO:0013757", "names": ["CHNG6", "congenital nongoitrous hypothyroidism 6", "congenital nongoitrous hypothryoidism 6", "hypothyroidism, congenital, nongoitrous, 6", "HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6", "THRA hypothyroidism, congenital, nongoitrous", "hypothyroidism, congenital, nongoitrous, type 6", "hypothyroidism, congenital, nongoitrous caused by mutation in THRA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital nongoitrous hypothryoidism 6", "shortest_name_length": 5}
{"curie": "MONDO:0003112", "names": ["Gastric Germ Cell Tumor", "Stomach Germ Cell Tumor", "Gastric Germ Cell Neoplasm", "Germ Cell Tumor of Stomach", "Stomach Germ Cell Neoplasm", "Germ Cell Neoplasm of Stomach", "Germ Cell Tumor of the Stomach", "germ cell tumor of the stomach", "germ cell tumour of the stomach", "Germ Cell Neoplasm of the Stomach", "Malignant Gastric Germ Cell Tumor", "malignant gastric germ cell tumor", "malignant gastric germ cell tumour", "Malignant Gastric Germ Cell Neoplasm", "malignant germ cell tumor of stomach", "Malignant Germ Cell Tumor of Stomach", "malignant gastric germ cell neoplasm", "Malignant Germ Cell Neoplasm of Stomach", "malignant germ cell neoplasm of stomach", "Malignant Germ Cell Tumor of the Stomach", "malignant germ cell tumor of the stomach", "Malignant Germ Cell Neoplasm of the Stomach", "malignant germ cell neoplasm of the stomach"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant gastric germ cell tumor", "shortest_name_length": 23}
{"curie": "MONDO:0009132", "names": ["Dysautonomia like disorder", "dysautonomia-like disorder", "Dysautonomia-Like Disorder", "dysautonomia like disorder", "DYSAUTONOMIA-LIKE DISORDER"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dysautonomia-like disorder", "shortest_name_length": 26}
{"curie": "UMLS:C3160947", "names": ["CNS toxicity", "Central nervous system toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "CNS toxicity", "shortest_name_length": 12}
{"curie": "UMLS:C1518077", "names": ["Lymphoma by Lukes-Collins Classification (Antiquated)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphoma by Lukes-Collins Classification (Antiquated)", "shortest_name_length": 53}
{"curie": "UMLS:C1371159", "names": ["Primary Cutaneous CD30+ T-Cell Lymphoproliferative Disorder", "Primary cutaneous CD30+ T-cell lymphoproliferative disorder", "Primary Cutaneous CD30-Positive T-Cell Lymphoproliferative Disorder", "primary cutaneous CD30 antigen positive T-cell lymphoproliferative disorder", "Primary cutaneous CD30 antigen positive T-cell lymphoproliferative disorder", "Primary cutaneous CD30 antigen positive T-cell lymphoproliferative disorder (disorder)", "primary cutaneous CD30 antigen positive T-cell lymphoproliferative disorder (diagnosis)", "Primary cutaneous CD30 antigen positive T-cell lymphoproliferative disorder (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary cutaneous CD30 antigen positive T-cell lymphoproliferative disorder", "shortest_name_length": 59}
{"curie": "MONDO:0022889", "names": ["craniostenosis with congenital heart disease intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniostenosis with congenital heart disease intellectual disability", "shortest_name_length": 68}
{"curie": "UMLS:C1336963", "names": ["Villous Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Villous Neoplasm", "shortest_name_length": 16}
{"curie": "UMLS:C1720824", "names": ["sudden cardiac arrest", "Sudden Cardiac Arrest", "Cardiac Arrest, Sudden", "Arrest, Sudden Cardiac", "Cardiac Arrests, Sudden", "sudden cardiac arrest (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sudden Cardiac Arrest", "shortest_name_length": 21}
{"curie": "UMLS:C4288034", "names": ["Vaginal Teratoma", "Vaginal Dermoid Cyst", "Vaginal Mature Cystic Teratoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Dermoid Cyst", "shortest_name_length": 16}
{"curie": "UMLS:C5204526", "names": ["Advanced Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Adenocarcinoma", "shortest_name_length": 23}
{"curie": "MONDO:0005915", "names": ["Tinea flava", "tinea flava", "tinea; flava", "flava; tinea", "Tinea Versicolor", "Tinea versicolor", "tinea versicolor", "TINEA VERSICOLOR", "Tinea versicolour", "versicolor; tinea", "tinea; versicolor", "tinea versicolour", "Pityriasis Versicolor", "pityriasis versicolor", "Pityriasis versicolor", "TV - Tinea versicolor", "versicolor; pityriasis", "pityriasis; versicolor", "Pityriasis versicolour", "pityriasis versicolour", "PV - Pityriasis versicolor", "Malassezia furfur Infection", "Malassezia furfur infection", "Malassezia furfur Infections", "Malassezia furfur; infection", "Infection, Malassezia furfur", "infection; Malassezia furfur", "tinea versicolor (diagnosis)", "infections, Malassezia furfur", "Infection by Malassezia furfur", "Infection by Pityrosporum furfur", "Pityriasis versicolor (disorder)", "infection by Pityrosporum furfur", "Pityrosporum orbiculare Infection", "Pityrosporum orbiculare Infections", "Infection, Pityrosporum orbiculare", "Tinea versicolor due to Malassezia furfur", "Pityriasis versicolor caused by Malassezia", "Tinea versicolor due to Pityrosporum furfur"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pityriasis versicolor", "shortest_name_length": 11}
{"curie": "MONDO:0007193", "names": ["Pbc", "PBC1", "Biliary Cirrhosis, Primary, 1", "primary biliary cholangitis 1", "BILIARY CIRRHOSIS, PRIMARY, 1", "biliary cirrhosis, primary, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary biliary cholangitis 1", "shortest_name_length": 3}
{"curie": "UMLS:C5399794", "names": ["Fibrohistiocytic Tumor", "Fibrohistiocytic Neoplasm", "Fibrohistiocytic neoplasm", "Fibrohistiocytic neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fibrohistiocytic Neoplasm", "shortest_name_length": 22}
{"curie": "MONDO:0005335", "names": ["colorectal tumor", "Colorectal Tumor", "colorectum tumor", "large bowel tumor", "Colorectal Tumors", "Tumor, Colorectal", "Large Bowel Tumor", "Tumors, Colorectal", "colorectum neoplasm", "tumor of colorectum", "Colorectal Neoplasm", "colorectal neoplasm", "Colorectal Neoplasms", "tumor of large bowel", "Large Bowel Neoplasm", "large bowel neoplasm", "Tumor of Large Bowel", "Neoplasm, Colorectal", "colorectal neoplasms", "Large intestine tumor", "Large Intestine Tumor", "Neoplasms, Colorectal", "large intestine tumor", "Large intestine tumour", "neoplasm of colorectum", "neoplasm of large bowel", "Neoplasm of large colon", "Neoplasm of Large Bowel", "tumor of the large bowel", "Tumor of large intestine", "Large Intestine Neoplasm", "Tumor of the Large Bowel", "large intestine neoplasm", "Tumour of large intestine", "large intestinal neoplasm", "Large Intestinal Neoplasm", "neoplasm of the large bowel", "Neoplasm of large intestine", "Neoplasm of the Large Bowel", "neoplasm of large intestine", "colorectum neoplasm (disease)", "Neoplasm of the large intestine", "Neoplasm of large colon (disorder)", "Neoplasm of large intestine (disorder)", "neoplasm of large intestine (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorectal neoplasm", "shortest_name_length": 16}
{"curie": "MONDO:0013037", "names": ["GIACHETI SYNDROME", "Giacheti Syndrome", "Giacheti syndrome", "Marfanoid habitus and specific language and learning disabilities", "Marfanoid Habitus and Specific Language and Learning Disabilities", "MARFANOID HABITUS AND SPECIFIC LANGUAGE AND LEARNING DISABILITIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Giacheti syndrome", "shortest_name_length": 17}
{"curie": "MONDO:0006655", "names": ["prolapse aortic valve", "Aortic valve prolapse", "Aortic Valve Prolapse", "aortic valve prolapse", "Valve Prolapse, Aortic", "Prolapse, Aortic Valve", "Aortic Valve Prolapses", "Valve Prolapses, Aortic", "Prolapses, Aortic Valve"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic valve prolapse", "shortest_name_length": 21}
{"curie": "UMLS:C0855050", "names": ["Metastatic Extraosseous Osteosarcoma", "Extraskeletal osteosarcoma metastatic", "Metastatic Extraskeletal Osteosarcoma", "Extraskeletal Osteosarcoma, Metastatic", "Metastatic Extraskeletal Osteogenic Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extraskeletal osteosarcoma metastatic", "shortest_name_length": 36}
{"curie": "MONDO:0014040", "names": ["OPTB8", "Autosomal Recessive Osteopetrosis 8", "autosomal recessive osteopetrosis 8", "osteopetrosis, autosomal recessive 8", "OSTEOPETROSIS, AUTOSOMAL RECESSIVE 8", "SNX10 autosomal recessive osteopetrosis", "autosomal recessive osteopetrosis type 8", "osteopetrosis, autosomal recessive type 8", "SNX10 autosomal recessive malignant osteopetrosis", "autosomal recessive osteopetrosis caused by mutation in SNX10", "autosomal recessive malignant osteopetrosis caused by mutation in SNX10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive osteopetrosis 8", "shortest_name_length": 5}
{"curie": "UMLS:C1706834", "names": ["Appendix Tubular Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Appendix Tubular Adenoma", "shortest_name_length": 24}
{"curie": "MONDO:0017729", "names": ["MLD, late infantile form", "arylsulfatase A deficiency, late infantile form", "metachromatic leukodystrophy, late infantile form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metachromatic leukodystrophy, late infantile form", "shortest_name_length": 24}
{"curie": "MONDO:0015995", "names": ["MSBD syndrome", "mixed sclerosing bone dystrophy", "Mixed sclerosing bone dystrophy", "dystrophy osseous sclerosing mixed", "OSTEOPOIKILOSIS WITH MELORHEOSTOSIS", "Melorheostosis with osteopoikilosis", "Melorheostosis with Osteopoikilosis", "melorheostosis with osteopoikilosis", "Melorheostosis with osteopoikilosis (disorder)", "MSBD (mixed sclerosing bone dystrophy) syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melorheostosis with osteopoikilosis", "shortest_name_length": 13}
{"curie": "MONDO:0013999", "names": ["ROSAH", "ROSAH syndrome", "Optic nerve edema-splenomegaly syndrome", "optic nerve edema-splenomegaly syndrome", "optic nerve edema, splenomegaly syndrome", "splenomegaly, cytopenia, and vision loss", "Optic nerve edema, splenomegaly syndrome", "SPLENOMEGALY, CYTOPENIA, AND VISION LOSS", "Optic nerve oedema, splenomegaly syndrome", "Optic nerve edema, splenomegaly syndrome (disorder)", "optic nerve edema, splenomegaly syndrome (diagnosis)", "Retinal dystrophy-optic nerve edema-splenomegaly-anhidrosis-migraine headache syndrome", "RETINAL DYSTROPHY, OPTIC NERVE EDEMA, SPLENOMEGALY, ANHIDROSIS, AND MIGRAINE HEADACHE SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "optic nerve edema-splenomegaly syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0238217", "names": ["Renal transplant rejection", "rejection renal transplant", "RENAL TRANSPLANT REJECTION", "renal transplant rejection", "kidney transplant rejection", "Kidney Transplant Rejection", "Acute Allograft Nephropathy", "kidney rejection transplant", "Acute allograft nephropathy", "Kidney transplant rejection", "kidney rejections transplant", "KIDNEY, TRANSPLANT REJECTION", "kidney transplant; rejection", "kidney rejection transplants", "rejection; transplant, kidney", "rejection of renal transplant", "kidneys rejection transplanted", "Acute Kidney Allograft Nephropathy", "Renal transplant rejection (disorder)", "renal transplant rejection (diagnosis)", "rejection of renal transplant (treatment)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal transplant rejection", "shortest_name_length": 26}
{"curie": "MONDO:0056814", "names": ["hormone-resistant prostate cancer", "Hormone-Resistant Prostate Cancer", "Hormone-Resistant Prostate Carcinoma", "hormone-resistant prostate carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hormone-resistant prostate carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0000671", "names": ["finger agnosia", "manual digit agnosia", "finger agnosia (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "finger agnosia", "shortest_name_length": 14}
{"curie": "MONDO:0044796", "names": ["spindle cell nevus", "Spindle Cell Nevus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spindle cell nevus", "shortest_name_length": 18}
{"curie": "UMLS:C0023474", "names": ["chronic phase CML", "Chronic Phase CML", "chronic phase CGL", "CGL, chronic phase", "CML, chronic phase", "Leukemia, Myeloid, Stable Phase", "Leukemia, Myeloid, Stable-Phase", "Leukemia, Myeloid, Chronic-Phase", "Leukemia, Myeloid, Chronic Phase", "myelocytic leukemia, chronic phase", "myelogenous leukemia, chronic phase", "Leukemia, Myelogenous, Chronic Phase", "Leukemia, Myelogenous, Chronic-Phase", "granulocytic leukemia, chronic phase", "Leukemia, Granulocytic, Chronic-Phase", "Leukemia, Granulocytic, Chronic Phase", "Chronic phase chronic myeloid leukemia", "Chronic Phase Chronic Myeloid Leukemia", "Chronic phase chronic myeloid leukaemia", "Myeloid Leukemia, Chronic, Stable-Phase", "Myeloid Leukemia, Chronic, Chronic-Phase", "chronic myeloid leukemia - chronic phase", "Myeloid Leukemia, Chronic, Chronic Phase", "Chronic Phase Chronic Myelocytic Leukemia", "chronic phase chronic myelogenous leukemia", "Chronic Phase Chronic Myelogenous Leukemia", "chronic myelocytic leukemia, chronic phase", "chronic myelogenous leukemia, chronic phase", "Chronic Phase Chronic Granulocytic Leukemia", "chronic myelogenous leukemia - chronic phase", "Granulocytic Leukemia, Chronic, Stable Phase", "Granulocytic Leukemia, Chronic, Stable-Phase", "Myelogenous Leukemia, Chronic, Chronic-Phase", "leukemia myelogenous chronic - chronic phase", "chronic granulocytic leukemia, chronic phase", "leukemia, chronic myelogenous, chronic phase", "Myelogenous Leukemia, Chronic, Chronic Phase", "Chronic phase chronic myeloid leukemia (disorder)", "chronic myelogenous leukemia - chronic phase (diagnosis)", "Chronic Phase Chronic Myelogenous Leukemia, BCR-ABL1 Positive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leukemia, Myeloid, Chronic-Phase", "shortest_name_length": 17}
{"curie": "MONDO:0001591", "names": ["senile entropion", "Senile entropion", "Age-related entropion", "involutional entropion", "Involutional entropion", "Senile entropion (disorder)", "senile entropion (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "senile entropion", "shortest_name_length": 16}
{"curie": "UMLS:C3670763", "names": ["Subcutaneous Edema", "SUBCUTANEOUS EDEMA", "Subcutaneous edema", "Edema, subcutaneous", "Subcutaneous edema (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subcutaneous edema", "shortest_name_length": 18}
{"curie": "MONDO:0024633", "names": ["HNP1", "NEPHROPATHY HYPERTENSIVE", "Hypertensive Nephropathy", "Hypertension;nephropathy", "hypertensive nephropathy", "Nephropathy hypertensive", "nephropathy hypertension", "Hypertensive nephropathy", "HYPERTENSIVE NEPHROPATHY", "Hypertensive renal disease", "hypertensive renal disease", "hypertension renal disease", "renal disease hypertension", "Hypertension;renal disease", "hypertensive kidney disease", "renal disease; hypertension", "Hypertensive nephropathy, NOS", "Hypertensive renal disease NOS", "Hypertensive renal disease, NOS", "Renal disease due to hypertension", "hypertensive nephropathy (diagnosis)", "Hypertensive renal disease (disorder)", "Hypertension secondary to renal disease", "Hypertensive renal disease, unspecified", "hypertensive kidney disease (diagnosis)", "hypertension secondary to renal disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertensive nephropathy", "shortest_name_length": 4}
{"curie": "MONDO:0021241", "names": ["Buccal Mucosa Tumor", "buccal mucosa tumor", "Tumor of cheek mucosa", "Buccal Mucosa Neoplasm", "tumor of buccal mucosa", "Tumor of buccal mucosa", "Tumor of Buccal Mucosa", "buccal mucosa neoplasm", "Tumour of cheek mucosa", "Tumour of buccal mucosa", "Neoplasm of buccal mucosa", "neoplasm of buccal mucosa", "Neoplasm of Buccal Mucosa", "Tumor of the Buccal Mucosa", "tumor of the buccal mucosa", "Neoplasm of the Buccal Mucosa", "neoplasm of the buccal mucosa", "buccal mucosa neoplasm (disease)", "Neoplasm of buccal mucosa (disorder)", "neoplasm of buccal mucosa (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "buccal mucosa neoplasm", "shortest_name_length": 19}
{"curie": "UMLS:C0861741", "names": ["Pancreatic adenocarcinoma recurrent", "Recurrent Pancreatic Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic adenocarcinoma recurrent", "shortest_name_length": 35}
{"curie": "MONDO:0030308", "names": ["IMD82", "immunodeficiency with systemic inflammation", "IMMUNODEFICIENCY 82 WITH SYSTEMIC INFLAMMATION", "immunodeficiency 82 with systemic inflammation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 82 with systemic inflammation", "shortest_name_length": 5}
{"curie": "MONDO:0008483", "names": ["STUT1", "STAMMERING", "stammering", "Stuttering, Familial Persistent 1", "STUTTERING, FAMILIAL PERSISTENT, 1", "stuttering, familial persistent, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stuttering, familial persistent, 1", "shortest_name_length": 5}
{"curie": "MONDO:0009646", "names": ["MLSM7", "M7MLS1", "Bone marrow monosomy 7", "chromosome 7Q deletion", "CHROMOSOME 7q DELETION", "MONOSOMY 7 OF BONE MARROW", "Monosomy 7 of Bone Marrow", "monosomy 7 of bone marrow", "Monosomy 7 Myelodysplasia and Leukemia Syndrome 1", "monosomy 7 myelodysplasia and leukemia syndrome 1", "MONOSOMY 7 MYELODYSPLASIA AND LEUKEMIA SYNDROME 1", "myelodysplasia and leukemia syndrome with monosomy 7", "Myelodysplasia and Leukemia Syndrome with Monosomy 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "monosomy 7 myelodysplasia and leukemia syndrome 1", "shortest_name_length": 5}
{"curie": "MONDO:0001835", "names": ["face palsy", "Facioplegia", "Facial Palsy", "facial droop", "Palsy;facial", "Facial palsy", "Facial droop", "FACIAL DROOP", "palsy facial", "facial palsy", "Bell's Palsy", "FACE WEAKNESS", "face weakness", "Palsy, Facial", "Face weakness", "palsy of face", "facial paresis", "Facial Paresis", "Facial Palsies", "Facial paresis", "facial drooping", "Palsy;VII nerve", "Facial weakness", "Palsies, Facial", "facial weakness", "VII nerve palsy", "Paresis, Facial", "Drooping;facial", "Pareses, Facial", "FACIAL PARALYSIS", "facial paralyses", "Weakness of face", "PARALYSIS FACIAL", "Facial paralysis", "Paralysis facial", "facial paralysis", "Facial Paralysis", "facial; paralysis", "Paralyses, Facial", "paralysis; facial", "Paralysis, Facial", "Facial Nerve Palsy", "VII th nerve palsy", "palsy facial nerve", "facial nerve palsy", "Facial nerve palsy", "seventh nerve palsy", "Facial nerve palsies", "muscle weakness face", "Facial Muscle Weakness", "FACIAL MUSCLE WEAKNESS", "facial nerve paralysis", "Facial nerve paralysis", "nerve disorders facial", "Facial Nerve Paralysis", "facial muscle weakness", "paralysis facial nerve", "Facial muscle weakness", "Facial palsy (disorder)", "Seventh nerve paralysis", "facial muscles weakness", "Cranial Nerve VII Palsy", "seventh nerve paralysis", "muscle weakness of face", "paralysis; facial nerve", "facial palsy (diagnosis)", "Weakness of face muscles", "Facial nerve paralysis, NOS", "Myasthenia of facial muscles", "Weakness of facial musculature", "Reduced facial muscle strength", "Weakness of the facial muscles", "Decreased facial muscle strength", "muscle weakness of face (symptom)", "Weakness of face muscles (finding)", "Decreased strength of facial muscles", "Facial nerve palsy (cranial nerve VII)", "Other late effects of cerebrovascular disease, facial weakness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "facial paralysis", "shortest_name_length": 10}
{"curie": "MONDO:0006711", "names": ["Pick Disease, Heart", "Heart Pick's Disease", "Picks Disease, Heart", "Pick disease of heart", "Pick Disease of Heart", "Pick syndrome of heart", "Pick's Disease of Heart", "Pick's disease of heart", "Constrictive Pericarditis", "Constrictive pericarditis", "PERICARDITIS CONSTRICTIVE", "constrictive pericarditis", "CONSTRICTIVE PERICARDITIS", "pericarditis constrictive", "Pericarditis constrictive", "pericarditis; constrictive", "PERICARDITIS, CONSTRICTIVE", "Pericarditis, Constrictive", "constrictive; pericarditis", "Constrictive Pericarditides", "Pericarditides, Constrictive", "constrictive pericarditis (disease)", "Constrictive pericarditis (disorder)", "constrictive pericarditis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "constrictive pericarditis", "shortest_name_length": 19}
{"curie": "MONDO:0009645", "names": ["Monocyte Chemotactic Disorder", "MONOCYTE CHEMOTACTIC DISORDER", "monocyte chemotactic disorder", "chronic mucocutaneous candidiasis due to monocyte chemotactic disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic mucocutaneous candidiasis due to monocyte chemotactic disorder", "shortest_name_length": 29}
{"curie": "UMLS:C4683233", "names": ["Clinical Stage II Retinoblastoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage II Retinoblastoma AJCC v8", "shortest_name_length": 40}
{"curie": "MONDO:0022568", "names": ["Bidirectional tachycardia", "bidirectional tachycardia", "Bidirectional ventricular tachycardia", "bidirectional ventricular tachycardia", "Bidirectional ventricular tachycardia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bidirectional tachycardia", "shortest_name_length": 25}
{"curie": "MONDO:0005306", "names": ["Bechterew", "Von Bechterew", "Marie-Strümpell", "Strümpell-Marie", "bechterew disease", "Bechterew Disease", "Bechterews disease", "Bechterews Disease", "Bekhterev syndrome", "Disease;Bechterews", "Bekhterev's disease", "bechterew's disease", "Bechterew's disease", "Bechterew's Disease", "Spondylosis Deformans", "Spondylosis deformans", "spondylosis deformans", "Rheumatoid Spondylitis", "rheumatoid spondylitis", "Ankylosing spondylitis", "Ankylosing Spondylitis", "Spondylitis ankylosing", "spondylitis ankylosing", "Rheumatoid spondylitis", "ANKYLOSING SPONDYLITIS", "SPONDYLITIS ANKYLOSING", "ankylosing spondylitis", "SPONDYLITIS, ANKYLOSING", "spondylitis; rheumatoid", "marie strumpell disease", "MARIE STRUMPELL DISEASE", "SPONDYLITIS, RHEUMATOID", "Marie-Strumpell disease", "spondylitis; ankylosing", "ankylosing; spondylitis", "rheumatoid; spondylitis", "Spondylitis, Ankylosing", "marie-strumpell disease", "Spondylitis, rheumatoid", "Spondylitis, Rheumatoid", "Marie Struempell Disease", "Marie-Struempell Disease", "Ankylosing polyarthritis", "arthritis rheumatoid spine", "spine rheumatoid arthritis", "Spondylitis ankylopoietica", "Spondylitis Ankylopoietica", "Marie Strumpell spondylitis", "ankylosing spondylarthritis", "spondylitis; ankylopoietica", "AS - Ankylosing spondylitis", "Ankylosing Spondylarthritis", "Marie-Strumpell spondylitis", "Ankylosing spondylitis, NOS", "ankylopoietica; spondylitis", "Marie Strümpell spondylitis", "rheumatoid; arthritis, spine", "MARIE-STRUEMPELL SPONDYLITIS", "Spondylitis, Marie-Strumpell", "arthritis; rheumatoid, spine", "spondylitis; Marie-Strümpell", "Spondylarthritis, Ankylosing", "Ankylosing Spondyloarthritis", "Marie-Strümpell; spondylitis", "Ankylosing Spondylarthritides", "Rheumatoid arthritis of spine", "Spondyloarthritis, Ankylosing", "Ankylosing Spondyloarthritides", "Spondylarthritides, Ankylosing", "Spondyloarthritides, Ankylosing", "spondylarthritis ankylopoietica", "Spondylarthritis Ankylopoietica", "Spondyloarthritis Ankylopoietica", "Ankylosing spondylitis (disorder)", "VON BECHTEREW-STRUEMPELL SYNDROME", "Idiopathic ankylosing spondylitis", "Rheumatioid arthritis of spine NOS", "Rheumatoid arthritis of spine, NOS", "ankylosing spondylitis (diagnosis)", "Bekhterev-Strumpell-Marie syndrome", "spine or vertebra; arthritis, ankylosing", "arthritis; spine or vertebra, ankylosing", "arthritis; spine or vertebra, Marie-Strümpell", "spine or vertebra; arthritis, Marie-Strümpell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ankylosing spondylitis", "shortest_name_length": 9}
{"curie": "MONDO:0003345", "names": ["Hilar CC", "Klatskin", "hilar CC", "hilar CCA", "Hilar CCA", "klatskin tumor", "klatzkin tumor", "Klatzkin tumor", "Klatskin Tumor", "Klatskin tumor", "Tumor, Klatskin", "Klatskin; tumor", "klatskins tumor", "tumor; Klatskin", "Klatskin tumour", "Klatskins Tumor", "klatskin tumors", "Klatskin's Tumor", "Klatskin's tumor", "klatskin's tumor", "klatskin's tumour", "Tumor, Klatskin's", "Klatskin's tumour", "Hilar Cholangiocarcinoma", "Hilar cholangiocarcinoma", "hilar cholangiocarcinoma", "Cholangiocarcinoma, Hilar", "Hilar Cholangiocarcinomas", "Cholangiocarcinomas, Hilar", "Klatskin's tumor morphology", "Klatskin's tumor (disorder)", "Perihilar Cholangiocarcinoma", "perihilar cholangiocarcinoma", "Klatskin's tumour morphology", "hilar cholangiocellular carcinoma", "Klatskin tumor (bile duct bifurcation)", "Perihilar extrahepatic bile duct carcinoma", "Klatskin's tumor (morphologic abnormality)", "perihilar extrahepatic bile duct carcinoma", "hilar portion of hepatic duct cholangiocarcinoma", "cholangiocarcinoma of hilar portion of hepatic duct"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hilar cholangiocarcinoma", "shortest_name_length": 8}
{"curie": "UMLS:C5667248", "names": ["Refractory Immunoblastic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Immunoblastic Lymphoma", "shortest_name_length": 33}
{"curie": "MONDO:0020148", "names": ["syndromic aniridia", "syndrome associated with aniridia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic aniridia", "shortest_name_length": 18}
{"curie": "UMLS:C5420060", "names": ["Sinonasal Hemangioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Hemangioma", "shortest_name_length": 20}
{"curie": "MONDO:0008889", "names": ["TAO", "tao", "taos", "Buerger", "Buerger Disease", "BUERGER disease", "BUERGER DISEASE", "Buerger disease", "buerger disease", "Buergers disease", "Disease, Buerger", "Buergers Disease", "Disease;Buergers", "buerger diseases", "buergers disease", "buergers diseases", "Buerger's disease", "buerger's disease", "Buerger's Disease", "presenile gangrene", "buergers's disease", "Presenile gangrene", "Disease, Buerger's", "Gangrene presenile", "GANGRENE, PRESENILE", "presenile; gangrene", "gangrene; presenile", "obliterans thromboangitis", "Thromboangitis obliterans", "Thromboangitis Obliterans", "thromboangitis obliterans", "obliterans thromboangiitis", "Thromboangiitis Obliterans", "WINIWARTER-BUERGER DISEASE", "THROMBOANGIITIS OBLITERANS", "thromboangiitis obliterans", "Thromboangiitis obliterans", "THROMBOANGIITIS, OBLITERANS", "thrombo angiitis obliterans", "Thrombo Angiitis Obliterans", "Presenile gangrene (disorder)", "Thromboangiitis obliterans [Buerger]", "Thromboangiitis obliterans (disorder)", "occlusive peripheral vascular disease", "thromboangiitis obliterans (diagnosis)", "Thromboangiitis obliterans (Buerger's disease)", "Thromboangiitis obliterans [Buerger's disease]", "thromboangiitis obliterans [Buerger's disease]", "thromboangiitis obliterans (Buerger's disease)", "inflammatory occlusive peripheral vascular disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thromboangiitis obliterans", "shortest_name_length": 3}
{"curie": "MONDO:0020387", "names": ["DORV-TGA", "Taussig-Bing syndrome", "DORV with subpulmonary VSD", "Double Outlet Right Ventricle, Subpulmonary VSD", "Double outlet right ventricle with transposition of the great arteries", "Double outlet right ventricle with subpulmonary ventricular septal defect", "double outlet right ventricle with subpulmonary ventricular septal defect", "Double outlet right ventricle with subpulmonary ventricular septal defect (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "double outlet right ventricle with subpulmonary ventricular septal defect", "shortest_name_length": 8}
{"curie": "MONDO:0021047", "names": ["Phyllodes Breast Tumor", "phyllodes breast tumor", "breast phyllodes tumor", "Breast Phyllodes Tumor", "Phyllodes Tumor of Breast", "Phyllodes tumor of breast", "Phyllodes Breast Neoplasm", "phyllodes breast neoplasm", "breast phyllodes neoplasm", "Breast Phyllodes Neoplasm", "phyllodes tumor of breast", "Phyllodes tumour of breast", "Phyllodes Neoplasm of Breast", "phyllodes neoplasm of breast", "breast cystosarcoma phyllodes", "Phyllodes Tumor of the Breast", "phyllodes tumor of the breast", "Phyllodes tumor of the breast", "Breast Cystosarcoma Phyllodes", "BREAST, CYSTOSARCOMA PHYLLODES", "BREAST, MYXOFIBROADENOMA, GIANT", "phyllodes neoplasm of the breast", "Phyllodes Neoplasm of the Breast", "Cystosarcoma phylloides - breast", "Cystosarcoma Phyllodes of Breast", "cystosarcoma phylloides - breast", "cystosarcoma phyllodes of breast", "cystosarcoma phyllodes of the breast", "Cystosarcoma Phyllodes of the Breast", "Phyllodes tumor of breast (disorder)", "Cystosarcoma phylloides of the breast", "cystosarcoma phylloides of the breast", "cystosarcoma phyllodes of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast phyllodes tumor", "shortest_name_length": 22}
{"curie": "UMLS:C4524437", "names": ["Laryngeal Cancer by AJCC v8 Stage", "Laryngeal Carcinoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laryngeal Cancer by AJCC v8 Stage", "shortest_name_length": 33}
{"curie": "MONDO:0017594", "names": ["indolent B-cell NHL", "Indolent B-cell NHL", "indolent B cell lymphoma", "B cell lymphoma, indolent", "indolent B-cell non-Hodgkin lymphoma", "Indolent B-cell non-Hodgkin lymphoma", "Indolent B-Cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "indolent B-cell non-Hodgkin lymphoma", "shortest_name_length": 19}
{"curie": "MONDO:0005187", "names": ["HHV8 Infection", "HHV8 infection", "Human Herpesvirus 8 Infection", "Human herpesvirus 8 infection", "human herpesvirus 8 infection", "Human Herpesvirus 8 infection", "Human Herpes Virus 8 Infection", "Human Herpes Virus 8 infection", "human herpesvirus 8 infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "human herpesvirus 8 infection", "shortest_name_length": 14}
{"curie": "MONDO:0021057", "names": ["classic or attenuated FAP", "classic or attenuated familial adenomatous polyposis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "classic or attenuated familial adenomatous polyposis", "shortest_name_length": 25}
{"curie": "UMLS:C0854265", "names": ["Post abortion bleeding", "Post abortion hemorrhage", "Post Abortion Hemorrhage", "Post abortion haemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post abortion hemorrhage", "shortest_name_length": 22}
{"curie": "UMLS:C2713347", "names": ["7-Dehydrocholesterol Reductase Deficiency", "Reductase Deficiency, 7-Dehydrocholesterol", "Deficiency, 7-Dehydrocholesterol Reductase", "7-Dehydrocholesterol Reductase Deficiencies", "Deficiencies, 7-Dehydrocholesterol Reductase", "Reductase Deficiencies, 7-Dehydrocholesterol"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "7-Dehydrocholesterol Reductase Deficiency", "shortest_name_length": 41}
{"curie": "UMLS:C1332468", "names": ["Benign Adult Cerebellar Tumor", "Benign Adult Cerebellar Tumors", "Benign Tumor of Adult Cerebellum", "Benign Adult Cerebellar Neoplasm", "Adult Benign Cerebellar Neoplasms", "Benign Neoplasm of Adult Cerebellum", "Benign Tumor of the Adult Cerebellum", "Benign Neoplasm of the Adult Cerebellum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Adult Cerebellar Neoplasm", "shortest_name_length": 29}
{"curie": "MONDO:0054700", "names": ["PRAAS2", "PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 2", "proteasome-associated autoinflammatory syndrome 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "proteasome-associated autoinflammatory syndrome 2", "shortest_name_length": 6}
{"curie": "UMLS:C1336915", "names": ["Endometrial Endometrioid Adenocarcinoma with a Poorly Differentiated Carcinomatous Component"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endometrial Endometrioid Adenocarcinoma with a Poorly Differentiated Carcinomatous Component", "shortest_name_length": 92}
{"curie": "MONDO:0016259", "names": ["Uterine Carcinosarcoma", "Uterine carcinosarcoma", "uterine carcinosarcoma", "Carcinosarcoma of Uterus", "carcinosarcoma of uterus", "Uterine Body Carcinosarcoma", "uterine body carcinosarcoma", "Carcinosarcoma of the Uterus", "carcinosarcoma of the uterus", "body of uterus carcinosarcoma", "uterine corpus carcinosarcoma", "Uterine Corpus Carcinosarcoma", "Carcinosarcoma of Uterine Body", "carcinosarcoma of uterine body", "Carcinosarcoma of corpus uteri", "Carcinosarcoma of Corpus Uteri", "carcinosarcoma of corpus uteri", "Uterine Mixed Müllerian Sarcoma", "uterine mixed Mullerian sarcoma", "Uterine Mixed Mullerian Sarcoma", "uterine mixed Müllerian sarcoma", "Carcinosarcoma of Uterine Corpus", "carcinosarcoma of uterine corpus", "Mixed Müllerian Sarcoma of Uterus", "Mixed Mullerian Sarcoma of Uterus", "mixed Müllerian sarcoma of uterus", "mixed Mullerian sarcoma of uterus", "Carcinosarcoma of the corpus uteri", "Carcinosarcoma of the Uterine Body", "carcinosarcoma of the corpus uteri", "Carcinosarcoma of the Corpus Uteri", "carcinosarcoma of the uterine body", "Carcinosarcoma of the Uterine Corpus", "carcinosarcoma of the uterine corpus", "mixed Mullerian sarcoma of the uterus", "Mixed Müllerian Sarcoma of the Uterus", "mixed Müllerian sarcoma of the uterus", "Mixed Mullerian Sarcoma of the Uterus", "mixed Mullerian cancer of corpus uteri", "Mixed Müllerian cancer of corpus uteri", "mixed Müllerian cancer of corpus uteri", "Uterine Malignant Mixed Mesodermal Tumor", "uterine malignant mixed mesodermal tumor", "Carcinosarcoma of corpus uteri (disorder)", "Malignant Mixed Mesodermal Tumor of Uterus", "malignant mixed mesodermal tumor of uterus", "Carcinosarcoma of corpus uteri (diagnosis)", "malignant mesodermal mixed tumor of uterus", "uterine malignant mixed mesodermal neoplasm", "Uterine Malignant Mixed Mesodermal Neoplasm", "Corpus Uteri Malignant Mixed Mesodermal Tumor", "Uterine Body Malignant Mixed Mesodermal Tumor", "uterine body malignant mixed mesodermal tumor", "malignant mixed mesodermal neoplasm of uterus", "Malignant Mixed Mesodermal Neoplasm of Uterus", "corpus uteri malignant mixed mesodermal tumor", "Malignant Mixed Mesodermal Tumor of the Uterus", "uterine corpus malignant mixed Müllerian tumor", "Uterine Corpus Malignant Mixed Mullerian Tumor", "Uterine Corpus Malignant Mixed Müllerian Tumor", "uterine corpus malignant mixed Mullerian tumor", "malignant mixed mesodermal tumor of the uterus", "uterine corpus malignant mixed mesodermal tumor", "Malignant mixed Müllerian tumor of corpus uteri", "Uterine Corpus Malignant Mixed Mesodermal Tumor", "malignant mixed müllerian tumor of corpus uteri", "Malignant mixed Müllerian tumour of corpus uteri", "malignant mixed mesodermal tumor of uterine body", "Malignant Mixed Mesodermal Tumor of Uterine Body", "Uterine Body Malignant Mixed Mesodermal Neoplasm", "uterine body malignant mixed mesodermal neoplasm", "Malignant Mixed Mesodermal Neoplasm of the Uterus", "Uterine Corpus Malignant Mixed Mullerian Neoplasm", "Uterine Corpus Malignant Mixed Müllerian Neoplasm", "uterine corpus malignant mixed Müllerian neoplasm", "malignant mixed mesodermal neoplasm of the uterus", "uterine corpus malignant mixed Mullerian neoplasm", "uterine corpus malignant mixed mesodermal neoplasm", "Uterine Corpus Malignant Mixed Mesodermal Neoplasm", "Malignant Mixed Mesodermal Tumor of Uterine Corpus", "Malignant mixed Müllerian neoplasm of corpus uteri", "malignant mixed mesodermal tumor of uterine corpus", "Malignant Mixed Mesodermal Neoplasm of Uterine Body", "Malignant mixed Müllerian tumor of the corpus uteri", "malignant mixed Mullerian tumor of the corpus uteri", "malignant mixed mesodermal neoplasm of uterine body", "malignant mixed Müllerian tumor of the corpus uteri", "Malignant Mixed Mesodermal Tumor of the Uterine Body", "malignant mixed mesodermal tumor of the uterine body", "Malignant Mixed Mesodermal Neoplasm of Uterine Corpus", "malignant mixed mesodermal neoplasm of uterine corpus", "malignant mixed mesodermal tumor of the uterine corpus", "uterine neoplasm malignant carcinosarcoma corpus uteri", "Malignant Mixed Mesodermal Tumor of the Uterine Corpus", "malignant mesodermal mixed tumor of uterus (diagnosis)", "malignant mixed mesodermal neoplasm of the uterine body", "Malignant Mixed Mesodermal Neoplasm of the Uterine Body", "malignant mixed mesodermal neoplasm of the uterine corpus", "Malignant Mixed Mesodermal Neoplasm of the Uterine Corpus", "Uterine Corpus Malignant Mixed Mesodermal (Müllerian) Tumor", "Uterine Corpus Malignant Mixed Mesodermal (Mullerian) Tumor", "uterine corpus malignant mixed mesodermal (Müllerian) tumor", "uterine corpus malignant mixed mesodermal (Mullerian) tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinosarcoma of the corpus uteri", "shortest_name_length": 22}
{"curie": "MONDO:0014410", "names": ["SCA37", "SPINOCEREBELLAR ATAXIA 37", "spinocerebellar ataxia 37", "spinocerebellar ataxia type 37", "Spinocerebellar ataxia type 37", "Spinocerebellar ataxia type 37 (disorder)", "Spinocerebellar ataxia with altered vertical eye movement", "spinocerebellar ataxia with altered vertical eye movements", "Spinocerebellar ataxia with altered vertical eye movements"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia type 37", "shortest_name_length": 5}
{"curie": "MONDO:0022754", "names": ["del(17p)", "deletion 17p", "17p monosomy", "17p deletion", "monosomy 17p", "17p- syndrome", "partial monosomy 17p", "deletion 17p syndrome", "Chromosome 17 deletion", "loss of chromosome 17p", "chromosome 17p deletion", "interstitial deletion 17p", "chromosome 17p deletion syndrome", "partial deletion of chromosome 17p", "partial monosomy of chromosome 17p", "partial monosomy of the short arm of chromosome 17", "partial deletion of the short arm of chromosome 17", "partial monosomy of the short arm of chromosome type 17"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 17p deletion", "shortest_name_length": 8}
{"curie": "MONDO:0013383", "names": ["HSCR3", "GDNF Hirschsprung disease", "Hirschsprung disease type 3", "Hirschsprung disease modifier", "susceptibility to Hirschsprung disease 3", "HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3", "Hirschsprung disease, susceptibility to, 3", "Hirschsprung disease caused by mutation in GDNF", "Hirschsprung disease, susceptibility to, type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hirschsprung disease, susceptibility to, 3", "shortest_name_length": 5}
{"curie": "MONDO:0002143", "names": ["yolk sac tumor", "vaginal yolk Sac tumor", "vaginal yolk sac tumor", "Vaginal Yolk Sac Tumor", "vaginal yolk Sac neoplasm", "vaginal Yolk Sac neoplasm", "Vaginal Yolk Sac Neoplasm", "vaginal endodermal sinus tumor", "Vaginal Endodermal Sinus Tumor", "Vaginal Endodermal Sinus Neoplasm", "vaginal endodermal sinus neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vaginal yolk sac tumor", "shortest_name_length": 14}
{"curie": "MONDO:0022634", "names": ["camptodactyly vertebral fusion", "Camptodactyly vertebral fusion", "Camptodactyly and sacral vertebral fusion", "camptodactyly and sacral vertebral fusion", "camptodactyly and sacral vertebral fusion (subtype)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "camptodactyly vertebral fusion", "shortest_name_length": 30}
{"curie": "MONDO:0003611", "names": ["uterine ligament papillary cystadenoma", "Uterine Ligament Papillary Cystadenoma Associated with von Hippel-Lindau Disease", "uterine ligament papillary cystadenoma associated with von Hippel-Lindau disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine ligament papillary cystadenoma associated with von Hippel-Lindau disease", "shortest_name_length": 38}
{"curie": "MONDO:0015443", "names": ["R8", "Ring 8", "r(8) syndrome", "rose cluster 8", "ROSE Cluster 8", "ring chromosome 8", "chromosome 8 ring", "Ring chromosome 8", "Chromosome 8 ring", "Ring Chromosome 8 Syndrome", "Ring chromosome 8 syndrome", "supernumerary ring/marker 8", "Ring chromosome 8 syndrome (disorder)", "Chromosome 8 derived supernumerary ring", "chromosome 8-derived supernumerary ring/marker"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 8-derived supernumerary ring/marker", "shortest_name_length": 2}
{"curie": "UMLS:C4054156", "names": ["Prevalent Nephrotic Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prevalent Nephrotic Syndrome", "shortest_name_length": 28}
{"curie": "UMLS:C0524611", "names": ["Cryptogenic Chronic Hepatitis", "Chronic Hepatitis, Cryptogenic", "Hepatitis, Cryptogenic Chronic", "Hepatitis, Chronic, Cryptogenic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cryptogenic Chronic Hepatitis", "shortest_name_length": 29}
{"curie": "UMLS:C1334156", "names": ["Immune System and Related Disorders", "Immunodeficiency and Immunosuppression Disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immune System and Related Disorders", "shortest_name_length": 35}
{"curie": "MONDO:0016547", "names": ["Beckwith-Wiedemann syndrome due to NSD1 mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Beckwith-Wiedemann syndrome due to NSD1 mutation", "shortest_name_length": 48}
{"curie": "MONDO:0012089", "names": ["IPS", "ichthyosis congenita 4", "Ichthyosis congenita IV", "ichthyosis congenita IV", "ICHTHYOSIS CONGENITA IV", "Congenital ichthyosis type 4", "congenital ichthyosis type 4", "Idiopathic pneumonia syndrome", "Idiopathic Pneumonia Syndrome", "idiopathic pneumonia syndrome", "ichthyosis-prematurity syndrome", "Ichthyosis-prematurity syndrome", "ICHTHYOSIS PREMATURITY SYNDROME", "ichthyosis prematurity syndrome", "Ichthyosis prematurity syndrome", "Idiopathic pneumonia syndrome (disorder)", "Ichthyosis prematurity syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ichthyosis prematurity syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0006182", "names": ["MANEC", "gastrointestinal MANEC", "Gastrointestinal MANEC", "Mixed adenoneuroendocrine carcinoma", "Mixed Adenoneuroendocrine Carcinoma", "mixed Adenoneuroendocrine carcinoma", "digestive system Mixed Adenoneuroendocrine cancer", "Digestive System Mixed Adenoneuroendocrine Cancer", "gastrointestinal mixed Adenoneuroendocrine carcinoma", "digestive system mixed adenoneuroendocrine carcinoma", "Digestive System Mixed Adenoneuroendocrine Carcinoma", "Gastrointestinal Mixed Adenoneuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "digestive system mixed adenoneuroendocrine carcinoma", "shortest_name_length": 5}
{"curie": "MONDO:0035008", "names": ["isolated splenic vein thrombosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated splenic vein thrombosis", "shortest_name_length": 32}
{"curie": "UMLS:C0752353", "names": ["Spinobulbar atrophy", "Atrophy, Muscular, Spinobulbar"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atrophy, Muscular, Spinobulbar", "shortest_name_length": 19}
{"curie": "UMLS:C0858540", "names": ["hemorrhage symptom", "Hemorrhage symptom", "Haemorrhage symptom", "hemorrhage symptoms", "hemorrhages symptoms"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Haemorrhage symptom", "shortest_name_length": 18}
{"curie": "MONDO:0006401", "names": ["salivary gland adenosquamous carcinoma", "Salivary Gland Adenosquamous Carcinoma", "adenosquamous carcinoma of salivary gland", "saliva-secreting gland adenosquamous carcinoma", "adenosquamous carcinoma of salivary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "salivary gland adenosquamous carcinoma", "shortest_name_length": 38}
{"curie": "MONDO:0018884", "names": ["Roch-Leri syndrome", "Roch-Leri mesosomatous lipomatosis", "Roch Leri mesosomatous lipomatosis", "Roch Leri mesosomatous lipomatosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Roch-Leri mesosomatous lipomatosis", "shortest_name_length": 18}
{"curie": "UMLS:C1334232", "names": ["Intestinal Gangliocytic Paraganglioma", "Gangliocytic Intestinal Paraganglioma", "Gangliocytic Paraganglioma of Intestine", "Gangliocytic Paraganglioma of the Intestine", "Intestinal Gangliocytic Neuroendocrine Tumor", "Intestinal Mixed Ganglioneuroma-Neuroendocrine Neoplasm", "Intestinal Composite Gangliocytoma/Neuroma and Neuroendocrine Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal Composite Gangliocytoma/Neuroma and Neuroendocrine Tumor", "shortest_name_length": 37}
{"curie": "UMLS:C1334799", "names": ["Monomorphic T-Cell PTLD", "Monomorphic T-Cell Post-Transplant Lymphoproliferative Disorder", "Monomorphic T/NK-Cell Post-Transplant Lymphoproliferative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Monomorphic T/NK-Cell Post-Transplant Lymphoproliferative Disorder", "shortest_name_length": 23}
{"curie": "UMLS:C4760934", "names": ["Transfusion Dependent Thalassemia", "Transfusion dependent thalassemia", "Transfusion-dependent Thalassemia", "Transfusion dependent thalassaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transfusion dependent thalassaemia", "shortest_name_length": 33}
{"curie": "MONDO:0023543", "names": ["Katsantoni-Papadakou-Lagoyanni syndrome", "Katsantoni Papadakou Lagoyanni syndrome", "Trichodermal syndrome and mental retardation", "Trichodermal syndrome and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Katsantoni-Papadakou-Lagoyanni syndrome", "shortest_name_length": 39}
{"curie": "UMLS:C1261287", "names": ["stenose", "stenosi", "stenosis", "stenoses", "Stenosis", "Stenoses", "Stricture", "stricture", "Strictures", "strictures", "Constriction", "STENOSIS NOS", "constriction", "Stenosis, NOS", "Stricture, NOS", "Constriction, NOS", "abnormal narrowing", "Pathologic Constriction", "Pathologic Constrictions", "Constriction, Pathologic", "Pathological Constriction", "Constrictions, Pathologic", "Constriction, Pathological", "Stenosis (morphologic abnormality)", "Stricture (morphologic abnormality)", "abnormal narrowing of a duct or passage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stenosis", "shortest_name_length": 7}
{"curie": "MONDO:0008833", "names": ["Rhpd", "RHPD", "RHPD1", "RENAL-HEPATIC-PANCREATIC DYSPLASIA 1", "renal-hepatic-pancreatic dysplasia 1", "NPHP3 renal-hepatic-pancreatic dysplasia", "renal-hepatic-pancreatic dysplasia type 1", "renal-hepatic-pancreatic dysplasia caused by mutation in NPHP3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal-hepatic-pancreatic dysplasia 1", "shortest_name_length": 4}
{"curie": "MONDO:0011044", "names": ["ectrodactyly of lower limbs, congenital heart defect, and micrognathia", "Ectrodactyly of Lower Limbs, Congenital Heart Defect, and Micrognathia", "ECTRODACTYLY OF LOWER LIMBS, CONGENITAL HEART DEFECT, AND MICROGNATHIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectrodactyly of lower limbs, congenital heart defect, and micrognathia", "shortest_name_length": 70}
{"curie": "UMLS:C2698737", "names": ["COL1A1 Associated Connective Tissue Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "COL1A1 Associated Connective Tissue Disorder", "shortest_name_length": 44}
{"curie": "MONDO:0019793", "names": ["ADCA3", "ADCAIII", "autosomal dominant cerebellar ataxia type 3", "autosomal dominant cerebellar ataxia type III", "Pure cerebellar syndrome-mild pyramidal signs syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant cerebellar ataxia type III", "shortest_name_length": 5}
{"curie": "UMLS:C3805220", "names": ["Hypervariability", "Marked Baseline Variability", "Exaggerated Baseline Variability", "Marked Baseline Fetal Heart Rate Variability", "Marked baseline fetal heart rate variability", "Marked baseline foetal heart rate variability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Marked baseline fetal heart rate variability", "shortest_name_length": 16}
{"curie": "UMLS:C3805222", "names": ["Pulmonary Vein Obstruction", "Pulmonary vein obstruction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pulmonary vein obstruction", "shortest_name_length": 26}
{"curie": "UMLS:C1336941", "names": ["Vaginal Non-Neoplastic Disease", "Vaginal Non-Neoplastic Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Non-Neoplastic Disorder", "shortest_name_length": 30}
{"curie": "MONDO:0022779", "names": ["cleft lip palate oligodontia syndactyly pili torti"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cleft lip palate oligodontia syndactyly pili torti", "shortest_name_length": 50}
{"curie": "MONDO:0005282", "names": ["Cutaneous Lupus Erythematosus", "cutaneous lupus erythematosus", "Cutaneous lupus erythematosus", "Lupus Erythematosus, Cutaneous", "lupus erythematosus, cutaneous", "Cutaneous lupus erythematosus, NOS", "Cutaneous lupus erythematosus (disorder)", "cutaneous lupus erythematosus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous lupus erythematosus", "shortest_name_length": 29}
{"curie": "MONDO:0012504", "names": ["CATSHLS", "CATSHL SYNDROME", "CATSHL syndrome", "Camptodactyly, tall stature, and hearing loss syndrome", "CAMPTODACTYLY, TALL STATURE, AND HEARING LOSS SYNDROME", "camptodactyly, tall stature, and hearing loss syndrome", "Camptodactyly-tall stature-scoliosis-deafness syndrome", "camptodactyly-tall stature-scoliosis-hearing loss syndrome", "Camptodactyly-tall stature-scoliosis-hearing loss syndrome", "CATSHL (camptodactyly, tall stature, scoliosis, hearing loss) syndrome", "Camptodactyly and tall stature with scoliosis and hearing loss syndrome", "Camptodactyly and tall stature with scoliosis and hearing loss syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "camptodactyly-tall stature-scoliosis-hearing loss syndrome", "shortest_name_length": 7}
{"curie": "UMLS:C5668168", "names": ["Peritoneal Primary Effusion Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peritoneal Primary Effusion Lymphoma", "shortest_name_length": 36}
{"curie": "MONDO:0007185", "names": ["BANKI SYNDROME", "Banki Syndrome", "Banki syndrome", "Banki syndrome (disorder)", "fusion of the lunate and cuneiform bones of the wrist, clinodactyly, clinometacarpy, brachymetacarpy and leptometacarpy (thin diaphysis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Banki syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0014328", "names": ["DEE19", "EIEE19", "early infantile epileptic encephalopathy 19", "Early Infantile Epileptic Encephalopathy 19", "Early Infantile epileptic encephalopathy 19", "epileptic encephalopathy, early infantile, 19", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 19", "Developmental and Epileptic Encephalopathy 19", "developmental and epileptic encephalopathy 19", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 19", "developmental and epileptic encephalopathy, 19", "GABRA1 early infantile epileptic encephalopathy", "epileptic encephalopathy, early infantile, type 19", "early infantile epileptic encephalopathy caused by mutation in GABRA1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 19", "shortest_name_length": 5}
{"curie": "MONDO:0002572", "names": ["chemical pneumonitis", "Chemical pneumonitis", "Mendelson's Syndrome", "aspiration pneumonia", "Aspiration Pneumonia", "Pneumonia, Aspiration", "Pneumonitis aspiration", "Aspiration pneumonitis", "Aspiration Pneumonitis", "ASPIRATION PNEUMONITIS", "aspiration pneumonitis", "Aspiration pneumonitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aspiration pneumonitis", "shortest_name_length": 20}
{"curie": "MONDO:0005076", "names": ["Pyorrhea", "Gum disease", "parodontitis", "Periodontitis", "periodontitis", "Periodontosis", "periodontosis", "Periodontoses", "PERIODONTITIS", "PERIODONTOSIS", "Periodontitides", "Periodontitis NOS", "Periodontitis, NOS", "Periodontal disease", "chronic pericementitis", "Periodontitis (disorder)", "periodontium inflammation", "periodontosis (diagnosis)", "periodontitis (diagnosis)", "Inflammation around tooth", "inflammation of periodontium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "periodontitis", "shortest_name_length": 8}
{"curie": "MONDO:0009111", "names": ["DPYSD", "DPH Deficiency", "DPH deficiency", "Dph deficiency", "DPH DEFICIENCY", "DPYS DEFICIENCY", "DPYS Deficiency", "DPYS deficiency", "Dpys deficiency", "dihydropyrimidinuria", "DIHYDROPYRIMIDINURIA", "Dihydropyrimidinuria", "Dihydropyrimidinurias", "Dihydropyrimidinase deficiency", "dihydropyrimidinase deficiency", "DIHYDROPYRIMIDINASE DEFICIENCY", "Dihydropyrimidinase Deficiency", "Dihydrouracil amidohydrolase deficiency", "Dihydropyrimidinase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dihydropyrimidinuria", "shortest_name_length": 5}
{"curie": "MONDO:0017865", "names": ["valvar pulmonary stenosis", "valvate pulmonary stenosis", "valvular pulmonary stenosis", "heart valve pulmonary stenosis", "congenital pulmonary valve stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital pulmonary valve stenosis", "shortest_name_length": 25}
{"curie": "UMLS:C1707986", "names": ["Extraocular Cutaneous Sebaceous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extraocular Cutaneous Sebaceous Carcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0013274", "names": ["RP51", "retinitis pigmentosa 51", "RETINITIS PIGMENTOSA 51", "TTC8 retinitis pigmentosa", "retinitis pigmentosa type 51", "retinitis pigmentosa caused by mutation in TTC8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 51", "shortest_name_length": 4}
{"curie": "UMLS:C1710274", "names": ["Syringoacanthoma", "Syringoacanthomas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Syringoacanthoma", "shortest_name_length": 16}
{"curie": "MONDO:0002370", "names": ["BRENNER TUMOR", "Brenner tumor", "Brenner; tumor", "tumor; Brenner", "Brenner tumor NOS", "Brenner tumor, NOS", "Brenner tumour NOS", "Brenner tumour, NOS", "ovary Brenner tumor", "Ovary Brenner Tumor", "OVARY, BRENNER TUMOR", "Ovarian Brenner Tumor", "ovarian Brenner tumor", "ovarian Brenner tumour", "Brenner tumor of ovary", "Brenner Tumor of Ovary", "OVARY, FIBROEPITHELIOMA", "Brenner tumour of ovary", "OVARIAN CANCER, BRENNER", "Ovarian Brenner Neoplasm", "ovarian Brenner neoplasm", "Brenner Neoplasm of Ovary", "Brenner neoplasm of ovary", "Brenner Tumor of the Ovary", "Brenner tumor of the ovary", "benign ovarian Brenner tumor", "benign ovarian Brenner tumour", "Brenner neoplasm of the ovary", "Brenner Neoplasm of the Ovary", "Ovarian Transitional Cell Tumor", "Brenner tumor of ovary (disorder)", "Ovarian Transitional Cell Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian Brenner tumor", "shortest_name_length": 13}
{"curie": "UMLS:C0751014", "names": ["Subcortical Infarction", "subcortical infarction", "Infarction, Subcortical", "Subcortical Infarctions", "Infarctions, Subcortical"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subcortical Infarction", "shortest_name_length": 22}
{"curie": "MONDO:0016541", "names": ["acquired secondary polycythemia", "acquired secondary erythrocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired secondary polycythemia", "shortest_name_length": 31}
{"curie": "MONDO:0023642", "names": ["Weber syndrome", "weber syndrome", "Weber Syndrome", "webers syndrome", "syndrome webers", "weber's syndrome", "Weber's syndrome", "Weber-Gubler syndrome", "Midbrain stroke syndromes", "Weber's syndrome (diagnosis)", "Weber-Gubler syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Weber syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0013003", "names": ["hypoglossia, isolated", "HYPOGLOSSIA, ISOLATED", "Hypoglossia, Isolated", "HYPOGLOSSIA WITH SITUS INVERSUS", "hypoglossia with situs inversus", "Hypoglossia With Situs Inversus", "isolated congenital hypoglossia/aglossia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated congenital hypoglossia/aglossia", "shortest_name_length": 21}
{"curie": "MONDO:0009196", "names": ["BADS", "BADS syndrome", "BADS Syndrome", "ERMINE PHENOTYPE", "Ermine phenotype", "ermine phenotype", "O'Doherty syndrome", "Pigmentary disorder with deafness", "Cutaneous albinism hermine phenotype", "Pigmentary disorder with hearing loss", "PIGMENTARY DISORDER WITH HEARING LOSS", "pigmentary disorder with hearing loss", "BLACK LOCKS WITH ALBINISM AND DEAFNESS SYNDROME", "Black Locks with Albinism and Deafness Syndrome", "black locks with albinism and deafness syndrome", "Black locks, oculocutaneous albinism, AND deafness of the sensorineural type", "Black locks, oculocutaneous albinism, and deafness of the sensorineural type", "black locks, oculocutaneous albinism, and deafness of the sensorineural type", "Black locks, oculocutaneous albinism, AND deafness of the sensorineural type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ermine phenotype", "shortest_name_length": 4}
{"curie": "MONDO:0013353", "names": ["MRAMS", "MRAMS syndrome", "mental retardation, anterior maxillary protrusion, and strabismus", "MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS", "intellectual disability, anterior maxillary protrusion, and strabismus", "Anterior maxillary protrusion-strabismus-intellectual disability syndrome", "Anterior maxillary protrusion, strabismus, intellectual disability syndrome", "MRAMS (mental retardation, anterior maxillary protrusion, strabismus) syndrome", "IMPAIRED INTELLECTUAL DEVELOPMENT, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS", "Anterior maxillary protrusion, strabismus, intellectual disability syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, anterior maxillary protrusion, and strabismus", "shortest_name_length": 5}
{"curie": "MONDO:0005350", "names": ["aaa", "AAA", "Abdominal aneurysm", "abdominal aneurysm", "aneurysm abdominal", "aneurysm; abdominal", "abdominal; aneurysm", "abdominal aneurysms", "Abdominal Aorta Aneurysm", "AORTA ABDOMINAL ANEURYSM", "abdominal aorta aneurysm", "abdominal aortic aneurysm", "Abdominal aortic aneurysm", "Aneurysm;abdominal aortic", "aneurysm; abdominal aorta", "Aorta Aneurysm, Abdominal", "Abdominal Aortic Aneurysm", "ABDOMINAL AORTIC ANEURYSM", "Aneurysm, Abdominal Aorta", "Abdominal Aorta Aneurysms", "Aortic Aneurysm, Abdominal", "Aneurysm, Abdominal Aortic", "Abdominal Aortic Aneurysms", "ANEURYSM, ABDOMINAL AORTIC", "abdominal aortic aneurysms", "ANEURYSM, AORTA, ABDOMINAL", "Aneurysm of abdominal aorta", "aorta abdominalis; aneurysm", "aneurysm of abdominal aorta", "AAA (abdominal aorta aneurysm)", "AAA (abdominal aortic aneurysm)", "abdominal aortic aneurysm (AAA)", "AAA - Abdominal aortic aneurysm", "Dilatation of the abdominal aorta", "Abdominal aortic aneurysm (disorder)", "aortic aneurysm, familial abdominal 1", "AORTIC ANEURYSM, FAMILIAL ABDOMINAL 1", "aneurysm of abdominal aorta (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "abdominal aortic aneurysm", "shortest_name_length": 3}
{"curie": "MONDO:0007719", "names": ["DIH1", "diaphragmatic hernia 1", "Diaphragmatic Hernia 1", "DIAPHRAGMATIC HERNIA 1", "hemidiaphragm, agenesis of", "DIAPHRAGM, COMPLETE AGENESIS OF", "Diaphragm, Complete Agenesis Of", "diaphragm, complete agenesis of", "diaphragmatic defect, congenital", "hernia, congenital diaphragmatic", "diaphragmatic hernia, congenital", "diaphragm, unilateral agenesis of", "diaphragmatic hernia, congenital 1", "hernia, congenital diaphragmatic 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diaphragmatic hernia 1", "shortest_name_length": 4}
{"curie": "MONDO:0019122", "names": ["IAEP", "PIE syndrome", "pie syndrome", "Loffler Syndrome", "Löffler syndrome", "Löffler Syndrome", "Loffler syndrome", "syndrome; Löffler", "loeffler syndrome", "Loeffler Syndrome", "LOEFFLER SYNDROME", "Loeffler syndrome", "Löffler; syndrome", "Löffler; pneumonia", "loefflers syndrome", "pneumonia; Löffler", "Loeffler's disease", "Löffler's syndrome", "loeffler's disease", "Syndrome, Loeffler", "Loffler's Syndrome", "Loffler's syndrome", "loffler's syndrome", "loeffler's syndrome", "Loeffler's syndrome", "LOEFFLER'S SYNDROME", "Löffler's pneumonia", "Loeffler's pneumonia", "Loeffler's Pneumonia", "loeffler's pneumonia", "acute eosinophilic pneumonia", "Acute eosinophilic pneumonia", "Pneumonia eosinophilic acute", "ACUTE EOSINOPHILIC PNEUMONIA", "Eosinophilic pneumonia acute", "Simple Pulmonary Eosinophilia", "simple pulmonary eosinophilia", "Simple pulmonary eosinophilia", "Löffler's syndrome (disorder)", "Pulmonary Eosinophilia, Simple", "Simple Pulmonary Eosinophilias", "Loeffler's syndrome (diagnosis)", "EP - Acute eosinophilic pneumonia", "EOSINOPHILIC PNEUMONIA ACUTE LOEFFLER", "pneumonia eosinophilic idiopathic acute", "pulmonary infiltrates with eosinophilia", "idiopathic acute eosinophilic pneumonia", "Idiopathic acute eosinophilic pneumonia", "EOSINOPHILIC PNEUMONIA ACUTE <LOEFFLER>", "acute eosinophilic pneumonia (diagnosis)", "pulmonary infiltration with eosinophilia (PIE)", "Idiopathic acute eosinophilic pneumonia (disorder)", "Idiopathic acute eosinophilic pneumonia (diagnosis)", "pulmonary infiltration with eosinophilia (PIE) (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic acute eosinophilic pneumonia", "shortest_name_length": 4}
{"curie": "UMLS:C4331230", "names": ["Recurrent Gliosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Gliosarcoma", "shortest_name_length": 21}
{"curie": "MONDO:0006720", "names": ["Cystic, mucinous and serous tumor", "Cystic, mucinous and serous tumour", "Cystic, Mucinous and Serous Neoplasms", "CYSTIC, MUCINOUS AND SEROUS NEOPLASMS", "cystic, mucinous, and serous neoplasm", "Cystic, Mucinous, and Serous Neoplasms", "Neoplasms, Cystic, Mucinous, and Serous"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cystic, mucinous, and serous neoplasm", "shortest_name_length": 33}
{"curie": "MONDO:0005359", "names": ["Toxic Hepatitis", "hepatitis toxic", "Toxic hepatitis", "HEPATITIS TOXIC", "toxic hepatitis", "Hepatitis toxic", "HEPATITIS, TOXIC", "Hepatitis, Toxic", "toxic; hepatitis", "hepatitis; toxic", "Toxic Hepatitides", "Hepatitides, Toxic", "drug-induced liver injury", "Toxic hepatitis (disorder)", "Toxin-associated hepatitis", "drug induced hepatotoxicity", "drug-induced disorder of liver", "Chemical and Drug Induced Liver Injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "drug-induced liver injury", "shortest_name_length": 15}
{"curie": "UMLS:C0563634", "names": ["M3v", "M3 Variant", "Hypogranular Acute Promyelocytic Leukemia", "Microgranular Acute Promyelocytic Leukemia", "leukemia acute promyelocytic - hypogranular variant", "Acute promyelocytic leukemia - hypogranular variant", "Acute promyelocytic leukaemia - hypogranular variant", "M3V - Acute promyelocytic leukemia - hypogranular variant", "M3V - Acute promyelocytic leukaemia - hypogranular variant", "Acute promyelocytic leukemia - hypogranular variant (disorder)", "Acute promyelocytic leukemia - hypogranular variant (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute promyelocytic leukemia - hypogranular variant", "shortest_name_length": 3}
{"curie": "MONDO:0012264", "names": ["PEE2", "preeclampsia/eclampsia 2", "PREECLAMPSIA/eclampsia 2", "Preeclampsia Eclampsia 2", "PREECLAMPSIA/ECLAMPSIA 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "preeclampsia/eclampsia 2", "shortest_name_length": 4}
{"curie": "MONDO:0001824", "names": ["polyneuropathy", "POLYNEUROPATHY", "Polyneuropathy", "Polyneuropathies", "polyneuropathies", "Polyneuropathy NOS", "Polyneuropathy, NOS", "neuropathy; multiple", "Acquired Polyneuropathy", "Acquired polyneuropathy", "Peripheral nerve disease", "Polyneuropathy, Acquired", "Acquired Polyneuropathies", "Polyneuropathy (disorder)", "Polyneuropathies, Acquired", "polyneuropathy (diagnosis)", "Polyneuropathy, unspecified", "Acquired polyneuropathy, NOS", "Polyneuropathy (multiple nerve disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyneuropathy", "shortest_name_length": 14}
{"curie": "MONDO:0020684", "names": ["EDS 8", "EDSPD1", "Ehlers-Danlos syndrome, type 8", "Ehlers-Danlos syndrome periodontal type 1", "Ehlers-Danlos syndrome, periodontosis type", "Ehlers-Danlos syndrome, periodontitis type", "Ehlers-Danlos syndrome, periodontal type 1", "Ehlers-Danlos syndrome, periodontal type, 1", "EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ehlers-Danlos syndrome, periodontal type 1", "shortest_name_length": 5}
{"curie": "MONDO:0003262", "names": ["Rhabdoid Meningioma", "Rhabdoid meningioma", "rhabdoid meningioma", "Papillary meningioma", "papillary meningioma", "meningioma, rhabdoid", "Meningioma, rhabdoid", "meningioma, rhabdoid (morphologic abnormality)", "papillary meningioma (morphologic abnormality)", "Meningioma, rhabdoid (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rhabdoid meningioma", "shortest_name_length": 19}
{"curie": "UMLS:C1285261", "names": ["Fetal Nutrition Disorder", "Nutrition Disorder, Fetal", "Fetal Nutrition Disorders", "Nutrition Disorders, Fetal", "Disorder of fetal nutrition", "Disorder of foetal nutrition", "Disorder of fetal nutrition (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fetal Nutrition Disorders", "shortest_name_length": 24}
{"curie": "MONDO:0021337", "names": ["Tonsil Cancer", "tonsil cancer", "carcinoma tonsil", "cancer of tonsil", "tonsillar cancer", "Tonsillar Cancer", "Tonsil carcinoma", "Cancer of Tonsil", "Tonsil Carcinoma", "tonsil carcinoma", "TONSIL, CARCINOMA", "carcinoma tonsils", "Carcinoma of Tonsil", "Tonsillar carcinoma", "tonsillar carcinoma", "Tonsillar Carcinoma", "carcinoma of tonsil", "Cancer of the Tonsil", "cancer of the tonsil", "Carcinoma of the Tonsil", "carcinoma of the tonsil", "Tonsil carcinoma (disorder)", "TONSILLAR CANCER, CARCINOMA", "carcinoma of tonsil (diagnosis)", "oropharyngeal neoplasm tonsil malignant carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tonsil carcinoma", "shortest_name_length": 13}
{"curie": "MONDO:0011260", "names": ["hereditary pancreas lymphoma", "PANCREATIC LYMPHOMA, FAMILIAL", "pancreatic lymphoma, familial", "Pancreatic Lymphoma, Familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic lymphoma, familial", "shortest_name_length": 28}
{"curie": "UMLS:C0855237", "names": ["Social avoidant behavior", "Social avoidant behaviour"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Social avoidant behavior", "shortest_name_length": 24}
{"curie": "MONDO:0010754", "names": ["van den Bosch syndrome", "Van den Bosch syndrome", "Van Den Bosch Syndrome", "VAN DEN BOSCH SYNDROME", "Van den Bosch syndrome (disorder)", "Van den Bosch syndrome (diagnosis)", "mental deficiency, choroideremia, acrokeratosis verruciformis,anhidrosis, skeletal deformity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "van den Bosch syndrome", "shortest_name_length": 22}
{"curie": "UMLS:C5206373", "names": ["Advanced Colon Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Colon Adenocarcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0001446", "names": ["URINARY URGENCY", "urgency urinary", "Urgency of mict", "Urinary Urgency", "urinary urgency", "Urinary urgency", "urgent urination", "Urination;urgent", "Urgency, urinary", "Urgency urination", "Urging to urinate", "Urination Urgency", "urgency urination", "urination urgency", "URGENCY URINATION", "Overactive Bladder", "hypertonic bladder", "overactive bladder", "bladder overactive", "Overactive bladder", "Hypertonic bladder", "MICTRUITION URGENT", "overactive; bladder", "Bladder instability", "Bladder, Overactive", "bladders overactive", "Hyperactive bladder", "Micturition urgency", "bladder; overactive", "Urgency - urination", "bladder hyperactive", "Micturition Urgency", "hyperactive bladder", "MICTURITION URGENCY", "Urgency of urination", "Urinary precipitancy", "URINATION URGENCY OF", "Urination urgency of", "Urgency to micturate", "Urgency to pass urine", "Precipitancy of urine", "bladder hyperactivity", "bladder hypertonicity", "hyperactivity bladder", "Instability of bladder", "Low bladder compliance", "Urgency with urination", "sudden urinary urgency", "low bladder compliance", "Urgency of micturition", "Low compliance bladder", "low compliance bladder", "hypertonicity of bladder", "Urgent desire to urinate", "Hyperactivity of bladder", "Hypertonicity of bladder", "lower bladder compliance", "hyperactivity of bladder", "Must hurry to pass urine", "Frequent/urgent urination", "Urinary frequency/urgency", "urinary urgency (symptom)", "URINARY URGENCY/FREQUENCY", "Urgency-frequency syndrome", "Urgency frequency syndrome", "Overactive Urinary Bladder", "Precipitancy of micturition", "Overactive bladder syndrome", "Urinary Bladder, Overactive", "feelings of urinary urgency", "Overactive bladder (disorder)", "Low compliance bladder (disorder)", "feelings of urinary urgency sudden", "Urgent desire to urinate (finding)", "feelings of sudden urinary urgency", "hyperactivity of bladder (diagnosis)", "lower bladder compliance (diagnosis)", "hypertonicity of bladder (diagnosis)", "feelings of sudden urinary urgency (symptom)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "low compliance bladder", "shortest_name_length": 15}
{"curie": "UMLS:C0431335", "names": ["Thoracic Myelocele", "Thoracic myelocele", "Thoracic myelocele (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thoracic myelocele", "shortest_name_length": 18}
{"curie": "MONDO:0008859", "names": ["CEREBRAL ANEURYSM-CIRRHOSIS SYNDROME", "cerebral aneurysm-cirrhosis syndrome", "Cerebral Aneurysm-Cirrhosis Syndrome", "BERRY ANEURYSM, CIRRHOSIS, PULMONARY EMPHYSEMA, AND CEREBRAL CALCIFICATION", "Berry Aneurysm, Cirrhosis, Pulmonary Emphysema, and Cerebral Calcification", "berry aneurysm, cirrhosis, pulmonary emphysema, and cerebral calcification"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "berry aneurysm, cirrhosis, pulmonary emphysema, and cerebral calcification", "shortest_name_length": 36}
{"curie": "UMLS:C0854963", "names": ["stage IV penile cancer", "penis cancer, stage IV", "penile cancer, stage IV", "Metastatic Penis Cancer", "Penis carcinoma stage IV", "Metastatic Penile Cancer", "metastatic penile cancer", "penis cancer, metastatic", "Metastatic penile cancer", "penile cancer, metastatic", "Metastatic Penis Carcinoma", "Metastatic cancer of penis", "Penis carcinoma metastatic", "Metastatic Penile Carcinoma", "Metastatic Carcinoma of Penis", "Metastatic Carcinoma of the Penis", "penile neoplasm malignant metastasis", "Metastasis from malignant tumor of penis", "Metastasis from malignant tumor of penis (disorder)", "Metastasis from malignant tumor of penis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Penile Cancer", "shortest_name_length": 22}
{"curie": "UMLS:C4763828", "names": ["Metastatic Bladder Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Bladder Squamous Cell Carcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0014727", "names": ["IMD45", "immunodeficiency 45", "IMMUNODEFICIENCY 45", "immunodeficiency type 45"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 45", "shortest_name_length": 5}
{"curie": "MONDO:0018552", "names": ["Urachal sinus", "urachal sinus", "Urachal sinus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urachal sinus", "shortest_name_length": 13}
{"curie": "UMLS:C0235774", "names": ["Neonatal drowsiness", "Neonatal somnolence", "Somnolence neonatal", "SOMNOLENCE NEONATAL", "Drowsiness of the newborn", "Somnolence of the newborn", "Drowsiness of the newborn (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drowsiness of the newborn", "shortest_name_length": 19}
{"curie": "MONDO:0016167", "names": ["optic tract glioma", "Optic tract glioma", "Optic pathway glioma", "optic pathway glioma", "glioma of optic tract", "Visual Pathway Glioma", "visual pathway glioma", "glioma of visual pathway", "Glioma of Visual Pathway", "glioma of the optic tract", "glioma of the visual pathway", "Glioma of the Visual Pathway"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "optic pathway glioma", "shortest_name_length": 18}
{"curie": "MONDO:0013674", "names": ["MPAN", "NBIA4", "NBIA due to C19orf12 mutation", "neurodegeneration with brain iron accumulation 4", "Neurodegeneration with Brain Iron Accumulation 4", "NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4", "Neurodegeneration with brain iron accumulation 4", "Neurodegeneration With Brain Iron Accumulation 4", "Mitochondrial Protein-Associated Neurodegeneration", "mitochondrial Protein-associated neurodegeneration", "MITOCHONDRIAL PROTEIN-ASSOCIATED NEURODEGENERATION", "Mitochondrial protein associated neurodegeneration", "neurodegeneration with brain iron accumulation type 4", "Neurodegeneration with brain iron accumulation type 4", "C19orf12 neurodegeneration with brain iron accumulation", "Mitochondrial membrane protein associated neurodegeneration", "Mitochondrial membrane protein-associated neurodegeneration", "mitochondrial membrane protein-associated neurodegeneration", "Mitochondrial membrane protein associated neurodegeneration (disorder)", "neurodegeneration with brain iron accumulation due to C19orf12 mutation", "Neurodegeneration with brain iron accumulation due to C19orf12 mutation", "neurodegeneration with brain iron accumulation caused by mutation in C19orf12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodegeneration with brain iron accumulation 4", "shortest_name_length": 4}
{"curie": "UMLS:C0729544", "names": ["CNS Fungal Infection", "Fungal Infection, CNS", "Infection, CNS Fungal", "CNS Fungal Infections", "Fungal Infections, CNS", "Infections, CNS Fungal", "Central Nervous System Mycoses", "Mycoses, Central Nervous System", "Central nervous system fungal infection", "Fungal central nervous system infection", "Central Nervous System Fungal Infections", "Fungal Infections, Central Nervous System", "Infections, Fungal, Central Nervous System", "Fungal infection of central nervous system", "Fungal infection of central nervous system (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Fungal Infections", "shortest_name_length": 20}
{"curie": "MONDO:0015397", "names": ["CFM", "HFM", "OAVD", "OAVS", "Goldenhar", "Fav sequence", "FAV SEQUENCE", "OAV spectrum", "OAV DYSPLASIA", "OAV dysplasia", "Goldenhar Disease", "Goldenhar disease", "syndrome goldenhar", "Goldenhar syndrome", "goldenhar syndrome", "Goldenhar sequence", "Goldenhar Syndrome", "GOLDENHAR SYNDROME", "goldenhars syndrome", "First arch syndrome", "first arch syndrome", "syndrome; first arch", "otofacial dysostosis", "Goldenhar's syndrome", "goldenhar's syndrome", "first arch; syndrome", "Hemifacial Microsomia", "hemifacial microsomia", "Hemifacial microsomia", "microsomia hemifacial", "Hemifacial hypoplasia", "HEMIFACIAL MICROSOMIA", "otomandibular syndrome", "Otomandibular syndrome", "craniofacial microsomia", "Craniofacial microsomia", "Craniofacial Microsomia", "CRANIOFACIAL MICROSOMIA", "Goldenhar syndrome (GS)", "lateral facial dysplasia", "otomandibular dysostosis", "Otomandibular dysostosis", "Lateral Facial Dysplasia", "Craniofacial Microsomias", "Microsomia, Craniofacial", "Otomandibular Dysostosis", "Goldenhar-Gorlin syndrome", "necrotic facial dysplasia", "Lateral Facial Dysplasias", "Shrinking of half of face", "Goldenhar Gorlin Syndrome", "Microsomias, Craniofacial", "Facial Dysplasia, Lateral", "Goldenhar-Gorlin Syndrome", "Dysplasia, Lateral Facial", "Dysostosis, Otomandibular", "oromandibulo-otic syndrome", "hemifacial microsomia (HM)", "Dysplasias, Lateral Facial", "Moeschler Clarren Syndrome", "Goldenhar-Gorlin Syndromes", "Facial Dysplasias, Lateral", "dysplasia oculo-auricularis", "intrauterine facial necrosis", "Goldenhar syndrome (disorder)", "First and second arch syndrome", "lateral facial dysplasia (LFD)", "oculoauriculovertebral spectrum", "Oculoauriculovertebral Syndrome", "oculoauriculovertebral syndrome", "OCULOAURICULOVERTEBRAL SPECTRUM", "Oculoauriculovertebral spectrum", "Facioauriculovertebral Sequence", "oromandibulo-auricular syndrome", "FACIOAURICULOVERTEBRAL SEQUENCE", "Oculoauriculovertebral Spectrum", "facioauriculovertebral sequence", "Goldenhar's syndrome (diagnosis)", "Facioauriculovertebral Dysplasia", "facio-auriculovertebral anomalad", "Oculoauriculovertebral Dysplasia", "oculoauriculovertebral dysplasia", "facioauriculovertebral dysplasia", "Hemifacial microsomia (disorder)", "OCULOAURICULOVERTEBRAL DYSPLASIA", "Decrease in size of half of face", "facio-auriculovertebral sequence", "Facioauriculovertebral Sequences", "Oculoauriculovertebral Spectrums", "oculo-auriculovertebral spectrum", "Franceschetti-Goldenhar syndrome", "Oculoauriculovertebral dysplasia", "Facio-auriculo-vertebral spectrum", "oculo-auriculo-vertebral spectrum", "oculo-auriculovertebral dysplasia", "facio-auriculo-vertebral spectrum", "hemignathia and microtia syndrome", "Oculoauriculovertebral Dysplasias", "Shrinking of one side of the face", "hemifacial microsomia (diagnosis)", "Dysplasia, Facioauriculovertebral", "Facio-auriculo-vertebral anomalad", "Oculo-auriculo-vertebral spectrum", "Facioauriculovertebral Dysplasias", "auriculobranchiogenital dysplasia", "Dysplasia, Oculoauriculovertebral", "Dysplasias, Facioauriculovertebral", "Decreased size of half of the face", "unilateral craniofacial microsomia", "Oral-Mandibular-Auricular Syndrome", "Dysplasias, Oculoauriculovertebral", "Oral Mandibular Auricular Syndrome", "Oculoauricular vertebral dysplasia", "oculo-auriculo-vertebral dysplasia", "Craniofacial microsomia (disorder)", "Otomandibular dysostosis (disorder)", "Oral-Mandibular-Auricular Syndromes", "otomandibular facial dysmorphogenesis", "unilateral mandibulofacial dysostosis", "facio-auriculovertebral (FAV) sequence", "OAV (oculoauriculovertebral) dysplasia", "Decreased size of one side of the face", "oculo-auriculovertebral (OAV) dysplasia", "unilateral intrauterine facial necrosis", "OAV (oculo-auriculo-vertebral) spectrum", "oculo-auriculovertebral spectrum (OAVS)", "Expanded spectrum hemifacial microsomia", "Decrease in size of one side of the face", "first and second branchial arch syndrome", "First and second branchial arch syndrome", "First and Second Branchial Arch Syndrome", "First AND second branchial arch syndrome", "Expanded spectrum of hemifacial microsomia", "First and Second Pharyngeal Arch Syndromes", "Facio-auriculo-vertebral spectrum (disorder)", "facio-auriculovertebral malformation complex", "Oculo-auriculo-vertebral spectrum (disorder)", "congenital deformity of head Goldenhar's syndrome", "First and second branchial arch syndrome (disorder)", "mandibulofacial dysostosis with epibulbar dermoids syndrome", "unilateral or bilateral and asymmetric otomandibular dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculo-auriculo-vertebral spectrum", "shortest_name_length": 3}
{"curie": "UMLS:C0752202", "names": ["Childhood Onset Dystonia", "Dystonia, childhood onset", "Dystonia, Childhood Onset", "Childhood Onset Dystonias", "Dystonias, Childhood Onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Onset Dystonias", "shortest_name_length": 24}
{"curie": "MONDO:0012160", "names": ["SMDCRD", "SMD-CRD", "SmD-CRD", "Spondylometaphyseal Dysplasia with Cone-Rod Dystrophy", "SPONDYLOMETAPHYSEAL DYSPLASIA WITH CONE-ROD DYSTROPHY", "spondylometaphyseal dysplasia with cone-rod dystrophy", "spondylometaphyseal dysplasia-cone-rod dystrophy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondylometaphyseal dysplasia-cone-rod dystrophy syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0002574", "names": ["Prostate Embryonal Rhabdomyosarcoma", "prostate embryonal rhabdomyosarcoma", "embryonal rhabdomyosarcoma of prostate", "Embryonal Rhabdomyosarcoma of Prostate", "prostate gland rhabdomyosarcoma embryonal", "Embryonal Rhabdomyosarcoma of the prostate", "Embryonal Rhabdomyosarcoma of the Prostate", "embryonal rhabdomyosarcoma of the prostate", "embryonal rhabdomyosarcoma of prostate (diagnosis)", "prostate gland embryonal rhabdomyosarcoma (disease)", "embryonal rhabdomyosarcoma (disease) of prostate gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate embryonal rhabdomyosarcoma", "shortest_name_length": 35}
{"curie": "MONDO:0017706", "names": ["disorder of carbohydrate absorption and transport", "disorder of carbohydrate transmembrane transport and absorption"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of carbohydrate transmembrane transport and absorption", "shortest_name_length": 49}
{"curie": "MONDO:0008702", "names": ["ACG2", "hypochondrogenesis", "Hypochondrogenesis", "achondrogenesis type 2", "Achondrogenesis type 2", "Type II Achondrogenesis", "achondrogenesis, type 2", "achondrogenesis type II", "Langer-Saldino dysplasia", "achondrogenesis, type IB", "ACHONDROGENESIS, TYPE II", "Achondrogenesis, type II", "achondrogenesis, type II", "Achondrogenesis, Type II", "Chondrogenesis imperfecta", "CHONDROGENESIS IMPERFECTA", "chondrogenesis imperfecta", "Langer-Saldino Achondrogenesis", "Langer-Saldino achondrogenesis", "Achondrogenesis syndrome, type II", "achondrogenesis, type IB, formerly", "ACHONDROGENESIS, TYPE IB, FORMERLY", "Achondrogenesis, type II (disorder)", "achondrogenesis, Langer-Saldino type", "Achondrogenesis, Langer-Saldino type", "ACHONDROGENESIS, LANGER-SALDINO TYPE", "achondrogenesis, type II or hypochondrogenesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "achondrogenesis type II", "shortest_name_length": 4}
{"curie": "UMLS:C5552708", "names": ["CAM", "BCEM", "Racial Melanosis", "Conjunctival Hypermelanosis", "Complexion-Associated Melanosis", "Primary Conjunctival Hypermelanosis", "Benign Conjunctival Epithelial Melanosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Racial Melanosis", "shortest_name_length": 3}
{"curie": "UMLS:C0854839", "names": ["Relapsed Angioimmunoblastic T-Cell Lymphoma", "Recurrent Angioimmunoblastic T-Cell Lymphoma", "Angioimmunoblastic T-cell lymphoma recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Angioimmunoblastic T-cell lymphoma recurrent", "shortest_name_length": 43}
{"curie": "MONDO:0002844", "names": ["lymphocytic gastritis", "Lymphocytic gastritis", "Lymphocytic Gastritis", "Lymphocytic gastritis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphocytic gastritis", "shortest_name_length": 21}
{"curie": "MONDO:0100375", "names": ["AML, t(15;17)(q24;q21)", "AML, t(15;17)(q22;q21)", "AML, t(15;17)(q22;q12)", "AML with a Variant RARA Translocation", "acute myeloid leukemia, t(15;17)(q24;q21)", "Acute Myeloid Leukemia with a Variant RARA Translocation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, t(15;17)(q24;q21)", "shortest_name_length": 22}
{"curie": "UMLS:C4526906", "names": ["Stage IIIB Soft Tissue Sarcoma of the Trunk and Extremities", "Stage IIIB Soft Tissue Sarcoma of the Trunk and Extremities AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Soft Tissue Sarcoma of the Trunk and Extremities AJCC v8", "shortest_name_length": 59}
{"curie": "MONDO:0009846", "names": ["PNTSU", "Pentosuria", "PENTOSURIA", "pentosuria", "Xylulosuria", "xylulosuria", "L-Xylulosuria", "L-xylulosuria", "L-XYLULOSURIA", "essential pentosuria", "Essential pentosuria", "xylulosuria (diagnosis)", "Essential benign pentosuria", "L-XYLULOSE REDUCTASE DEFICIENCY", "L-xylulose reductase deficiency", "L-Xylulose reductase deficiency", "Essential pentosuria (disorder)", "XYLITOL DEHYDROGENASE DEFICIENCY", "xylitol dehydrogenase deficiency", "deficiency dehydrogenase xylitol", "Xylitol dehydrogenase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pentosuria", "shortest_name_length": 5}
{"curie": "MONDO:0003302", "names": ["epithelioid neurofibroma", "Epithelioid neurofibroma", "Epithelioid Neurofibroma", "Epithelioid neurofibroma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epithelioid neurofibroma", "shortest_name_length": 24}
{"curie": "UMLS:C4763761", "names": ["Locally Advanced Urothelial Cancer", "Locally Advanced Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Urothelial Carcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0009390", "names": ["periodic hyperlysinemia", "Periodic hyperlysinemia", "Periodic Hyperlysinemia", "Periodic hyperlysinaemia", "Periodic Hyperlysinemias", "HYPERLYSINEMIA, PERIODIC", "hyperlysinemia, periodic", "Hyperlysinemia, Periodic", "Hyperlysinemias, Periodic", "Periodic hyperlysinemia (disorder)", "Hyperlysinuria With Hyperammonemia", "Hyperlysinuria with hyperammonemia", "HYPERLYSINURIA WITH HYPERAMMONEMIA", "hyperlysinuria with hyperammonemia", "With Hyperammonemia, Hyperlysinuria", "Hyperammonemia, Hyperlysinuria With", "Hyperlysinuria with hyperammonaemia", "periodic hyperlysinemia (diagnosis)", "Hyperlysinuria With Hyperammonemias", "Hyperammonemias, Hyperlysinuria With", "With Hyperammonemias, Hyperlysinuria", "Periodic hyperlysinemia with hyperammonemia", "Periodic hyperlysinaemia with hyperammonaemia", "Periodic hyperlysinemia with hyperammonemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperlysinuria with hyperammonemia", "shortest_name_length": 23}
{"curie": "MONDO:0017807", "names": ["GTS", "growing teratoma syndrome", "Growing teratoma syndrome", "Growing Teratoma Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "growing teratoma syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0029132", "names": ["LIDLS3", "Liddle syndrome 3", "LIDDLE SYNDROME 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liddle syndrome 3", "shortest_name_length": 6}
{"curie": "UMLS:C2733359", "names": ["Tics/Tremor", "Psychogenic tremor", "psychogenic tremor", "Psychogenic Tremor", "Psychogenic tremor (disorder)", "psychogenic tremor (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Psychogenic tremor", "shortest_name_length": 11}
{"curie": "UMLS:C0861598", "names": ["Stage II Mouth Epidermoid Carcinoma", "Stage II Epidermoid Carcinoma of Mouth", "Stage II Mouth Squamous Cell Carcinoma", "Stage II Oral Cavity Squamous Cell Cancer", "Stage II Squamous Cell Carcinoma of Mouth", "Stage II Oral Cavity Epidermoid Carcinoma", "Stage II Epidermoid Carcinoma of the Mouth", "Stage II Epidermoid Carcinoma of Oral Cavity", "Stage II Oral Cavity Squamous Cell Carcinoma", "Stage II Squamous Cell Carcinoma of the Mouth", "Stage II Squamous Cell Carcinoma of Oral Cavity", "Stage II Epidermoid Carcinoma of the Oral Cavity", "Squamous cell carcinoma of the oral cavity stage II", "Stage II Squamous Cell Carcinoma of the Oral Cavity", "Stage II Oral Cavity Squamous Cell Carcinoma AJCC v6", "Stage II Oral Cavity Squamous Cell Carcinoma AJCC v7", "Stage II Oral Cavity Squamous Cell Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Squamous cell carcinoma of the oral cavity stage II", "shortest_name_length": 35}
{"curie": "MONDO:0009913", "names": ["Prune belly syndrome with pulmonic stenosis, mental retardation and deafness", "Prune Belly Syndrome with Pulmonic Stenosis, Mental Retardation, and Deafness", "prune belly syndrome with pulmonic stenosis, mental retardation, and deafness", "PRUNE BELLY SYNDROME WITH PULMONIC STENOSIS, MENTAL RETARDATION, AND DEAFNESS", "prune belly syndrome with pulmonic stenosis, intellectual disability, deafness", "Prune belly syndrome with pulmonic stenosis, intellectual disability and deafness", "prune belly syndrome with pulmonic stenosis, intellectual disability, and deafness", "Prune belly syndrome with pulmonic stenosis, intellectual disability and deafness (disorder)", "prune belly syndrome with pulmonic stenosis, intellectual disability, and deafness (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prune belly syndrome with pulmonic stenosis, intellectual disability, and deafness", "shortest_name_length": 76}
{"curie": "MONDO:0018189", "names": ["autosomal recessive cerebellar ataxia - pyramidal signs - nystagmus - oculomotor apraxia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive cerebellar ataxia - pyramidal signs - nystagmus - oculomotor apraxia syndrome", "shortest_name_length": 97}
{"curie": "UMLS:C1707539", "names": ["Cusp tear", "Cusp Tear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cusp tear", "shortest_name_length": 9}
{"curie": "UMLS:C0854524", "names": ["Peridiverticular abscess"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peridiverticular abscess", "shortest_name_length": 24}
{"curie": "UMLS:C5206479", "names": ["Locally Advanced Unresectable Colon Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Unresectable Colon Adenocarcinoma", "shortest_name_length": 50}
{"curie": "MONDO:0013644", "names": ["CMT2O", "DYNC1H1 Charcot-Marie-Tooth disease", "Charcot-Marie-Tooth disease type 2O", "Charcot-Marie-Tooth disease axonal type 2O", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2O", "Charcot-Marie-Tooth disease, axonal, type 2O", "Charcot-Marie-Tooth disease, axonal, type 20", "Charcot-Marie-Tooth neuropathy axonal type 2O", "CHARCOT-MARIE-TOOTH NEUROPATHY, AXONAL, TYPE 2O", "Charcot-Marie-Tooth neuropathy, axonal, type 2O", "Autosomal dominant Charcot-Marie-Tooth disease type 2O", "autosomal dominant Charcot-Marie-Tooth disease type 2O", "Charcot-Marie-Tooth disease caused by mutation in DYNC1H1", "autosomal dominant axonal Charcot-Marie-Tooth disease type 2O", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2O", "Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2O", "Autosomal dominant Charcot-Marie-Tooth disease type 2O (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease axonal type 2O", "shortest_name_length": 5}
{"curie": "MONDO:0013956", "names": ["IMD31A", "IMMUNODEFICIENCY 31A", "immunodeficiency 31A", "immunodeficiency type 31A", "Stat1 deficiency, autosomal dominant", "MSMD due to partial STAT1 deficiency", "STAT1 DEFICIENCY, AUTOSOMAL DOMINANT", "autosomal dominant immunodeficiency 31A, mycobacteriosis", "IMMUNODEFICIENCY 31A, MYCOBACTERIOSIS, AUTOSOMAL DOMINANT", "immunodeficiency 31A, Mycobacteriosis, autosomal dominant", "MSMD due to partial signal transducer and activator of transcription 1 deficiency", "Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency", "STAT1 autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency", "autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency caused by mutation in STAT1", "Mendelian susceptibility to mycobacterial diseases due to partial signal transducer and activator of transcription 1 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency", "shortest_name_length": 6}
{"curie": "MONDO:0020290", "names": ["ECD", "AVSD", "AVCD", "AVC DEFECT", "AVC Defect", "Common AV Canal", "common AV canal", "AV septal defect", "AV Septal Defect", "Atrioventricular canal", "canal atrioventricular", "atrioventricular canal", "Hole in center of heart", "Hole in centre of heart", "endocardial cushion defect", "Endocardial cushion defect", "Endocardial Cushion Defect", "ENDOCARDIAL CUSHION DEFECT", "cushion defect; endocardium", "Cushion Defect, Endocardial", "Endocardial Cushion Defects", "Defect, Endocardial Cushion", "Endocardial cushion defects", "endocardial cushion defects", "endocardium; cushion defect", "cushion, endocardial; defect", "Cushion Defects, Endocardial", "Defects, Endocardial Cushion", "defect; cushion, endocardial", "Atrioventricular Canal Defect", "atrioventricular canal defect", "Common Atrioventricular Canal", "common atrioventricular canal", "ATRIOVENTRICULAR CANAL DEFECT", "Atrioventricular canal defect", "Atrioventricular canal defects", "Atrioventricular Septal Defect", "defect; atrioventricular canal", "ATRIOVENTRICULAR SEPTAL DEFECT", "Atrioventricular septal defect", "Endocardial cushion defect NOS", "atrioventricular septal defect", "Atrioventricular septal defects", "atrioventricular defects septal", "canal; atrioventricular, defect", "Endocardial cushion defect, NOS", "defect; atrioventricular septum", "atrioventricular; canal, defect", "defect; septum, atrioventricular", "atrioventricular; septum, defect", "septum; atrioventricular, defect", "septum; defect, atrioventricular", "atrioventricular canal (diagnosis)", "Endocardial cushion defect (disorder)", "AVSD - Atrioventricular septal defect", "Atrioventricular septal defect (AVSD)", "endocardial cushion defect (diagnosis)", "familial atrioventricular septal defect", "atrioventricular septal defect (diagnosis)", "Endocardial cushion defect, unspecified type", "congenital heart defect atrioventricular septal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial atrioventricular septal defect", "shortest_name_length": 3}
{"curie": "MONDO:0012339", "names": ["CELIAC4", "MYO9B celiac disease", "susceptibility to celiac disease 4", "celiac disease, susceptibility to, 4", "CELIAC DISEASE, SUSCEPTIBILITY TO, 4", "celiac disease, susceptibility to, type 4", "celiac disease caused by mutation in MYO9B", "gluten-sensitive enteropathy, susceptibility to, 4", "GLUTEN-SENSITIVE ENTEROPATHY, SUSCEPTIBILITY TO, 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "celiac disease, susceptibility to, 4", "shortest_name_length": 7}
{"curie": "MONDO:0003984", "names": ["Inner Ear Lipoma", "inner Ear lipoma", "internal Ear lipoma", "Internal Ear Lipoma", "Internal Auditory Canal Lipoma", "internal auditory canal lipoma", "internal acoustic meatus lipoma", "lipoma of internal auditory canal", "Lipoma of Internal Auditory Canal", "lipoma of internal acoustic meatus", "Lipoma of the Internal Auditory Canal", "Lipoma of the Internal Auditory canal", "lipoma of the internal auditory canal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "internal auditory canal lipoma", "shortest_name_length": 16}
{"curie": "MONDO:0005302", "names": ["ADD", "ADHD", "addh", "ADDH", "MBD syndrome", "Attention deficit", "Attention-deficit", "deficit; attention", "Attention deficits", "hyperactivity; child", "child; hyperactivity", "hyperkinetic syndrome", "Hyperkinetic syndrome", "Syndrome hyperkinetic", "HYPERKINETIC SYNDROME", "Hyperkinetic Syndrome", "Hyperkinetic disorder", "SYNDROME HYPERKINETIC", "hyperkinetic disorder", "hyperkinetic; syndrome", "hyperkinetic; disorder", "hyperactivity disorder", "disorder hyperactivity", "syndrome; hyperkinetic", "Hyperkinetic disorders", "disorder; hyperkinetic", "disorder; hyperactivity", "Minimal Brain Disorders", "hyperactivity; disorder", "Syndromes, Hyperkinetic", "Hyperkinetic syndrome NOS", "minimal brain dysfunction", "MINIMAL BRAIN DYSFUNCTION", "Minimal Brain Dysfunction", "Minimal brain dysfunction", "Overactive child syndrome", "Hyperactive child syndrome", "Attention-deficit disorder", "hyperactive child syndrome", "ATTENTION DEFICIT DISORDER", "Brain Dysfunction, Minimal", "Attention Deficit Disorder", "Hyperactivity Disorder NOS", "Attention deficit disorder", "attention-deficit disorder", "attention deficit disorder", "Dysfunction, Minimal Brain", "HYPERACTIVITY OF CHILDHOOD", "attention deficit disorders", "Attention Deficit Disorders", "Disorder, Attention Deficit", "Deficit Disorder, Attention", "disorder; attention deficit", "Deficit Disorders, Attention", "Disorders, Attention Deficit", "Minimal brain damage syndrome", "add attention deficit disorder", "attention deficit disorder add", "Attention-Deficit Disorder NOS", "Disorder;attent deficit(hyper)", "Childhood hyperkinetic syndrome", "childhood hyperkinetic syndrome", "MBD - Minimal brain dysfunction", "ADD - Attention deficit disorder", "attention deficit hyper disorder", "attention deficit(hyper) disorder", "attention deficits disorder hyper", "Unspecified hyperkinetic syndrome", "Minimal brain dysfunction syndrome", "Hyperkinetic disorder, unspecified", "Hyperkinetic syndrome of childhood", "ADHD, predominantly inattentive type", "Attention deficit without hyperactivity", "Attention deficit hyperkinetic disorder", "Attention deficit-hyperactivity disorder", "Attention Deficit-Hyperactivity Disorder", "ATTENTION DEFICIT-HYPERACTIVITY DISORDER", "Attention Deficit Hyperactivity Disorder", "ATTENTION DEFICIT HYPERACTIVITY DISORDER", "attention deficit hyperactivity disorder", "attention-deficit hyperactivity disorder", "Attention deficit hyperactivity disorder", "Attention-deficit/hyperactivity disorder", "Attention-deficit hyperactivity disorder", "Attention deficit/hyperactivity disorder", "Attention-deficit hyperactivity disorders", "Disorder, Attention Deficit-Hyperactivity", "Attention Deficit-Hyperactivity Disorders", "Deficit-Hyperactivity Disorder, Attention", "Attention Deficit Hyperactivity Disorders", "Disorders, Attention Deficit-Hyperactivity", "Deficit-Hyperactivity Disorders, Attention", "Attention-deficit hyperactivity disorder NOS", "Attention deficit/hyperactivity disorder NOS", "attention deficit disorder with hyperactivity", "Attention deficit disorder with hyperactivity", "attention deficit syndrome with hyperactivity", "Attention Deficit Disorder with Hyperactivity", "unspecified hyperkinetic syndrome of childhood", "ADHD, predominantly hyperactive-impulsive type", "Unspecified hyperkinetic syndrome of childhood", "Attention Deficit Disorders with Hyperactivity", "attention deficit disorder; with hyperactivity", "ADHD (attention-deficit hyperactivity disorder)", "Attention-deficit/hyperactivity disorder (ADHD)", "Attention deficit hyperactivity disorder (ADHD)", "attention deficit hyperactivity disorder (ADHD)", "ADHD (attention deficit hyperactivity disorder)", "Attention-deficit hyperactivity disorder (ADHD)", "Attention deficit-hyperactivity disorder (ADHD)", "Attention deficit disorder without hyperactivity", "ADHD, predominantly inattentive type (diagnosis)", "attention deficit disorder without hyperactivity", "attention deficit disorder; without hyperactivity", "Childhood attention deficit/hyperactivity disorder", "ADD - Attention deficit disorder with hyperactivity", "Attention deficit hyperactivity disorder (disorder)", "ADHD - Attention deficit disorder with hyperactivity", "attention-deficit hyperactivity disorder (diagnosis)", "disorder; attention deficit, with hyperactivity (ADHD)", "ADD - Attention deficit disorder without hyperactivity", "Attention deficit disorder with hyperactivity syndrome", "Attention deficit disorder without hyperactivity syndrome", "attention-deficit disorder predominantly inattentive type", "Attention-Deficit Disorder, Predominantly Inattentive Type", "Attention Deficit Hyperactivity Disorder, Inattentive Type", "unspecified hyperkinetic syndrome of childhood (diagnosis)", "Attention deficit disorder of childhood with hyperactivity", "attention deficit hyperactivity disorder, inattentive type", "Attention deficit disorder without mention of hyperactivity", "attention deficit disorder without hyperactivity (diagnosis)", "Hyperactivity Disorder, Predominantly Hyperactive-Impulsive Type", "Attention-Deficit Disorder, Predominantly Hyperactive-Impulsive Type", "Attention deficit hyperactivity disorder, hyperactive impulsive type", "attention deficit hyperactivity disorder, inattentive/distractible type", "attention-deficit hyperactivity disorder predominantly inattentive type", "Attention Deficit Hyperactivity Disorder, Inattentive/Distractible Type", "Attention Deficit Hyperactivity Disorder, Predominantly Inattentive Type", "Attention deficit disorder of childhood without mention of hyperactivity", "Attention deficit hyperactivity disorder, predominantly inattentive type", "attention deficit hyperactivity disorder, predominantly inattentive type", "Attention-deficit hyperactivity disorder, predominantly inattentive type", "Attention deficit hyperactivity disorder, predominantly hyperactive impulsive type", "Attention deficit hyperactivity disorder, predominantly inattentive type (disorder)", "Attention deficit hyperactivity disorder, predominantly hyperactive impulsive type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "attention deficit hyperactivity disorder, inattentive type", "shortest_name_length": 3}
{"curie": "MONDO:0014881", "names": ["SDDHD", "TKT DEFICIENCY", "TKT deficiency", "Transketolase deficiency", "TRANSKETOLASE DEFICIENCY", "transketolase deficiency", "TKT (transketolase) deficiency", "SHORT STATURE, DEVELOPMENTAL DELAY, AND CONGENITAL HEART DEFECTS", "short stature, developmental delay, and congenital heart defects", "Short stature-developmental delay-congenital heart defect syndrome", "short stature-developmental delay-congenital heart defect syndrome", "Short stature, developmental delay, congenital heart defect syndrome", "Short stature, developmental delay, congenital heart defect syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transketolase deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0011767", "names": ["DFNB31", "Whirler, Mouse, Homolog Of", "WHIRLER, MOUSE, HOMOLOG OF", "whirler, mouse, homolog of", "autosomal recessive deafness 31", "DEAFNESS, AUTOSOMAL RECESSIVE 31", "Deafness, Autosomal Recessive 31", "deafness, autosomal recessive 31", "deafness, autosomal recessive type 31", "autosomal recessive nonsyndromic deafness 31", "WHRN autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 31", "autosomal recessive nonsyndromic deafness type 31", "autosomal recessive nonsyndromic deafness caused by mutation in WHRN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 31", "shortest_name_length": 6}
{"curie": "UMLS:C0854530", "names": ["HHV6 Infection", "HHV-6 Infection", "human herpesvirus 6 infection", "Human herpesvirus 6 infection", "Human Herpesvirus-6 Infection", "Human Herpes Virus-6 Infection", "Infection by human herpesvirus 6", "Infection caused by human herpesvirus 6", "human herpesvirus 6 infection (diagnosis)", "Infection caused by human herpesvirus 6 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infection by human herpesvirus 6", "shortest_name_length": 14}
{"curie": "MONDO:0015337", "names": ["isolated craniosynostosis", "nonsyndromic craniosynostosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated craniosynostosis", "shortest_name_length": 25}
{"curie": "MONDO:0021187", "names": ["lipemia", "lipemias", "lipidemia", "Lipidemia", "lipidaemia", "lipidemias", "Lipidaemia", "lipoidemia", "HYPERLIPEMIA", "hyperlipemia", "Hyperlipemia", "hyperlipemias", "Hyperlipemias", "Hyperlipaemia", "HYPERLIPAEMIA", "HYPERLIPIDEMIA", "hyperlipidemia", "Hyperlipidemia", "hyperlipidaemia", "Hyperlipidemias", "Hyperlipidaemia", "hyperlipidemias", "hyperlipidaemias", "Hyperlipidemia NOS", "Hyperlipidemia, NOS", "Hyperlipidaemia NOS", "HLD - Hyperlipidemia", "Hyperlipidaemia, NOS", "HLD - Hyperlipidaemia", "hyperlipidemia (disease)", "Elevated lipids in blood", "Hyperlipidemia (disorder)", "excessive fat in the blood", "Hyperlipidemia, unspecified", "Hyperlipidaemia, unspecified", "Disorder characterized by hyperlipidemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperlipidemia", "shortest_name_length": 7}
{"curie": "UMLS:C0264914", "names": ["bifascicular BBB", "BIFASCICULAR BLOCK", "Bifascicular block", "Bifascicular Block", "bifascicular block", "bifascicular; block", "block; bifascicular", "Bifascicular block NOS", "Bifascicular block, NOS", "Bifascicular block (disorder)", "bifascicular bundle branch block", "BUNDLE BRANCH BLOCK BIFASCICULAR", "Bifascicular Bundle Branch Block", "Bifascicular Block by ECG Finding", "Bifascicular Block by EKG Finding", "bifascicular bundle branch block (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bifascicular block", "shortest_name_length": 16}
{"curie": "MONDO:0001571", "names": ["Gynecomazia", "gynecomastia", "Gynecomastia", "Gynaecomazia", "GYNECOMASTIA", "gynaecomastia", "Gynaecomastia", "GYNAECOMASTIA", "Enlarged male breast", "gynecomastia disorder", "gynecomastia (symptom)", "Male Breast Enlargement", "Enlargement breast male", "BREAST ENLARGEMENT MALE", "male breast enlargement", "ENLARGEMENT BREAST MALE", "Breast enlargement male", "Gynecomastia (disorder)", "gynecomastia (diagnosis)", "Enlargement, Male Breast", "Breast Enlargement, Male", "Hypertrophy of male breast", "Mammary enlargement in male", "male organism hypertrophy of breast", "hypertrophy of breast of male organism", "Gynecomastia of non-human mammary gland", "Gynecomastia of non-human mammary gland (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gynecomastia disorder", "shortest_name_length": 11}
{"curie": "UMLS:C0312854", "names": ["Extravascular Hemolysis", "Extravascular Hemolyses", "Extravascular hemolysis", "HEMOLYSIS EXTRAVASCULAR", "Hemolyses, Extravascular", "Hemolysis, Extravascular", "Extravascular haemolysis", "Extravascular hemolysis (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extravascular Hemolysis", "shortest_name_length": 23}
{"curie": "UMLS:C1334005", "names": ["High Grade Malignant Peripheral Nerve Sheath Tumor", "Poorly Differentiated Malignant Peripheral Nerve Sheath Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Malignant Peripheral Nerve Sheath Tumor", "shortest_name_length": 50}
{"curie": "UMLS:C1881585", "names": ["pancreatic G-cell carcinoma", "gastrin producing carcinoma", "gastrin secreting carcinoma", "Pancreatic G-Cell Carcinoma", "G-cell carcinoma, pancreatic", "carcinoma, pancreatic G-cell", "G-cell, pancreatic carcinoma", "pancreas; malignant gastrinoma", "gastrinoma; malignant, pancreas", "Malignant Pancreatic Gastrinoma", "malignant pancreatic gastrinoma", "malignant; gastrinoma, pancreas", "pancreas; gastrinoma, malignant", "malignant gastrinoma of pancreas", "Malignant gastrinoma of pancreas", "pancreas; G cell tumor, malignant", "tumor; G cell, malignant, pancreas", "G cell; tumor, malignant, pancreas", "Malignant G cell neoplasm of pancreas", "Malignant gastrinoma of pancreas (disorder)", "malignant gastrinoma of pancreas (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant gastrinoma of pancreas", "shortest_name_length": 27}
{"curie": "UMLS:C0022373", "names": ["Jejunal Disease", "Disease, Jejunal", "Jejunal Diseases", "Diseases, Jejunal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jejunal Diseases", "shortest_name_length": 15}
{"curie": "MONDO:0014911", "names": ["GRIDHH", "growth retardation, impaired intellectual development, hypotonia, and hepatopathy", "GROWTH RETARDATION, IMPAIRED INTELLECTUAL DEVELOPMENT, HYPOTONIA, AND HEPATOPATHY", "Growth retardation, intellectual developmental disorder, hypotonia, and hepatopathy", "growth retardation, intellectual developmental disorder, hypotonia, and hepatopathy", "growth retardation, intellectual developmental disorder, hypotonia, and hepatopathy; GRIDHH"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "growth retardation, intellectual developmental disorder, hypotonia, and hepatopathy", "shortest_name_length": 6}
{"curie": "MONDO:0035892", "names": ["Mills syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mills syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C3273076", "names": ["Extrarenal Rhabdoid Tumor of the Liver", "Extrarenal Malignant Rhabdoid Tumor of the Liver"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extrarenal Rhabdoid Tumor of the Liver", "shortest_name_length": 38}
{"curie": "MONDO:0044625", "names": ["CMT2 due to DGAT2 mutation", "autosomal dominant charcot-marie-tooth disease type 2 due to DGAT2 mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant charcot-marie-tooth disease type 2 due to DGAT2 mutation", "shortest_name_length": 26}
{"curie": "UMLS:C0269398", "names": ["Miscarriage with sepsis", "Pregnancy loss with sepsis", "Spontaneous abortion with sepsis", "Miscarriage with sepsis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Miscarriage with sepsis", "shortest_name_length": 23}
{"curie": "UMLS:C0677949", "names": ["Colorectal cancer Dukes C", "Colorectal cancer stage III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal cancer stage III", "shortest_name_length": 25}
{"curie": "MONDO:0012293", "names": ["DFNB23", "autosomal recessive deafness 23", "DEAFNESS, AUTOSOMAL RECESSIVE 23", "Deafness, Autosomal Recessive 23", "deafness, autosomal recessive 23", "deafness, autosomal recessive type 23", "autosomal recessive nonsyndromic deafness 23", "PCDH15 autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 23", "autosomal recessive nonsyndromic deafness type 23", "autosomal recessive nonsyndromic deafness caused by mutation in PCDH15"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 23", "shortest_name_length": 6}
{"curie": "MONDO:0013968", "names": ["GSD14", "CDG1T", "CDGIt", "CDG-It", "GSD 14", "GSDXIV", "CDG It", "CDG it", "GSD XIV", "PGM1-CDG", "GSD type 14", "PGM1 Deficiency", "Pgm1 deficiency", "PGM1 DEFICIENCY", "CDG syndrome type It", "type 14 glycogenosis", "glycogen storage disease 14", "GLYCOGEN STORAGE DISEASE XIV", "Glycogen Storage Disease XIV", "phosphoglucomutase 1 deficiency", "Phosphoglucomutase 1 Deficiency", "PHOSPHOGLUCOMUTASE 1 DEFICIENCY", "Phosphoglucomutase-1 deficiency", "phosphoglucomutase-1 deficiency", "phosphoglucomutase deficiency type 1", "congenital disorder of glycosylation 1t", "congenital disorder of glycosylation It", "PGM1-congenital disorder of glycosylation", "Congenital disorder of glycosylation type 1t", "Congenital disorder of glycosylation type It", "congenital disorder of glycosylation type 1t", "congenital disorder of glycosylation type It", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE It", "congenital disorder of glycosylation, type It", "PGM1-related congenital disorder of glycosylation", "glycogen storage disease due to phosphoglucomutase deficiency", "Phosphoglucomutase 1-related congenital disorder of glycosylation", "Phosphoglucomutase 1-related congenital disorder of glycosylation (disorder)", "PGM1-CDG - Phosphoglucomutase 1-related congenital disorder of glycosylation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PGM1-congenital disorder of glycosylation", "shortest_name_length": 5}
{"curie": "MONDO:0017630", "names": ["SPG1", "X-linked complicated spastic paraplegia type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked complicated spastic paraplegia type 1", "shortest_name_length": 4}
{"curie": "UMLS:C0877635", "names": ["CMV viremia", "CMV viraemia", "Cytomegalovirus viremia", "Cytomegalovirus viraemia", "Cytomegalovirus viremia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cytomegalovirus viremia", "shortest_name_length": 11}
{"curie": "MONDO:0019188", "names": ["RSTS", "Rubinstein-Taybi", "rubinstein syndrome", "RUBINSTEIN SYNDROME", "Rubinstein Syndrome", "Rubinstein syndrome", "Syndrome, Rubinstein", "rubenstein-taybi syndrome", "rubenstein taybi syndrome", "RUBENSTEIN-TAYBI SYNDROME", "Rubinstein-Taybi syndrome", "rubinstein taybi syndrome", "syndrome rubinstein taybi", "Rubinstein-Taybi Syndrome", "Rubinstein Taybi Syndrome", "rubinstein-taybi syndrome", "rubinstein taybis syndrome", "Syndrome, Rubinstein-Taybi", "Broad Thumb Hallux Syndrome", "Broad Thumb-Hallux syndrome", "BROAD THUMB-HALLUX SYNDROME", "broad thumb-hallux syndrome", "Broad Thumb-Hallux Syndrome", "Broad thumb-hallux syndrome", "Syndrome, Broad Thumb-Hallux", "Broad Thumb-Hallux Syndromes", "Syndromes, Broad Thumb-Hallux", "Broad thumbs-halluces syndrome", "Rubinstein-Taybi syndrome (disorder)", "Rubinstein-Taybi syndrome (RSTS, RTS)", "Rubinstein-Taybi syndrome (diagnosis)", "broad thumb-mental retardation syndrome", "proximal chromosome 16p13.3 deletion syndrome", "Broad Thumbs and Great Toes, Characteristic Facies, and Mental Retardation", "BROAD THUMBS AND GREAT TOES, CHARACTERISTIC FACIES, AND MENTAL RETARDATION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rubinstein-Taybi syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0012758", "names": ["HPC13", "MSMB familial prostate cancer", "PROSTATE CANCER, HEREDITARY, 13", "Prostate Cancer, Hereditary, 13", "prostate cancer, hereditary, 13", "prostate cancer, hereditary, type 13", "familial prostate cancer caused by mutation in MSMB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate cancer, hereditary, 13", "shortest_name_length": 5}
{"curie": "UMLS:C4552924", "names": ["Stage IB Ovarian Cancer", "Stage IB Ovarian Cancer AJCC v8", "Stage IB Ovarian Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Ovarian Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "UMLS:C1142083", "names": ["Nicolau syndrome", "Nicolau Syndrome", "nicolau syndrome", "Syndrome, Nicolau", "Nicolaus Syndrome", "Nicolau's Syndrome", "Syndrome, Nicolau's", "Livedo-like Dermatitis", "Livedo like Dermatitis", "Dermatitis, Livedo-like", "Livedo-like Dermatitides", "Dermatitides, Livedo-like", "Nicolau Livedoid Syndrome", "Nicolaus Livedoid Syndrome", "embolia cutis medicamentosa", "Embolia cutis medicamentosa", "Nicolau Livedoid Dermatitis", "Nicolau's Livedoid Syndrome", "Embolia Cutis Medicamentosa", "Medicamentosa, Embolia Cutis", "Syndrome, Nicolau's Livedoid", "Livedoid Syndrome, Nicolau's", "Livedoid Dermatitis, Nicolau", "Cutis Medicamentosa, Embolia", "Dermatitis, Nicolau Livedoid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nicolau Syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0010987", "names": ["NSRD8", "DFNB8", "NRSD8", "DFNB10", "autosomal recessive deafness 8", "DEAFNESS, AUTOSOMAL RECESSIVE 8", "deafness, autosomal recessive 8", "autosomal recessive deafness 10", "Deafness, Autosomal Recessive 10", "deafness, autosomal recessive 10", "DEAFNESS, AUTOSOMAL RECESSIVE 10", "deafness, autosomal recessive 8/10", "deafness, autosomal recessive type 8", "autosomal recessive nonsyndromic deafness 8", "Neurosensory Nonsyndromic Recessive Deafness 8", "NEUROSENSORY NONSYNDROMIC RECESSIVE DEAFNESS 8", "neurosensory nonsyndromic recessive deafness 8", "autosomal recessive nonsyndromic hearing loss 8", "autosomal recessive nonsyndromic deafness type 8", "childhood-onset neurosensory autosomal recessive deafness 8", "DEAFNESS, CHILDHOOD-ONSET NEUROSENSORY, AUTOSOMAL RECESSIVE 8", "deafness, childhood-onset neurosensory, autosomal recessive 8", "Deafness, Childhood-Onset Neurosensory, Autosomal Recessive 8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 8", "shortest_name_length": 5}
{"curie": "UMLS:C1336297", "names": ["Stage II Lymphocyte Depleted Hodgkin Lymphoma", "Stage II Hodgkin's Lymphoma Lymphocyte Depleted", "Stage II Lymphocyte Depleted Hodgkin's Lymphoma", "Stage II Hodgkin's Disease Lymphocyte Depletion Type", "Stage II Hodgkin's Lymphoma Lymphocyte Depletion Type", "Stage II Lymphocyte-Depleted Classical Hodgkin Lymphoma", "Stage II Lymphocyte Depleted Classical Hodgkin Lymphoma", "Ann Arbor Stage II Lymphocyte-Depleted Classic Hodgkin Lymphoma", "Ann Arbor Stage II Lymphocyte-Depleted Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ann Arbor Stage II Lymphocyte-Depleted Classic Hodgkin Lymphoma", "shortest_name_length": 45}
{"curie": "MONDO:0007402", "names": ["elevate cpk", "increased ck", "elevated cpk", "CK increased", "cpk increase", "increase cpk", "CPK ELEVATED", "cpk elevated", "CPK increase", "Increased CPK", "CPK INCREASED", "cpk increased", "CPK increased", "Increased serum CK", "Elevated serum CPK", "CPK, ELEVATED SERUM", "CPK, elevated serum", "high creatine kinase", "Creatine kinase high", "creatine high kinases", "hyperCKemia, idiopathic", "HYPERCKEMIA, IDIOPATHIC", "Increased phosphokinase", "Elevated creatine kinase", "Increased creatine kinase", "Creatine kinase increased", "CREATINE KINASE INCREASED", "creatine kinase increased", "increased creatine kinase", "CK concentration increased", "High serum creatine kinase", "CPK concentration increased", "Raised creatine kinase level", "Increase serum creatine kinase", "Elevated serum creatine kinase", "Elevated creatine kinase level", "Increased creatine kinase level", "Increased serum creatine kinase", "Elevated creatine kinase levels", "Creatine Phosphokinase Increased", "Increased creatine phosphokinase", "Creatine phosphokinase increased", "CREATINE PHOSPHOKINASE SERUM INC", "Creatine kinase, serum, elevated", "CREATINE PHOSPHOKINASE INCREASED", "Increased CK (creatine kinase) level", "creatine kinase increased (lab test)", "SERUM CREATINE PHOSPHOKINASE ELEVATED", "Elevated serum creatine phosphokinase", "Elevated blood creatine phosphokinase", "Phosphokinase creatine serum increased", "Creatine phosphokinase serum increased", "Increased creatine phosphokinase (CPK)", "Blood creatine phosphokinase increased", "Increased serum creatine phosphokinase", "creatine phosphokinase, elevated serum", "PHOSPHOKINASE CREATINE SERUM INCREASED", "Serum creatine phosphokinase increased", "CREATINE PHOSPHOKINASE, ELEVATED SERUM", "Plasma creatine phosphokinase increased", "Creatine kinase level above reference range", "Elevated circulating creatine phosphokinase", "Creatine phosphokinase concentration increased", "Elevated circulating creatine kinase concentration", "Creatine kinase level above reference range (finding)", "hematology nonspecific abnormal findings creatine kinase increased"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "creatine phosphokinase, elevated serum", "shortest_name_length": 11}
{"curie": "UMLS:C0009938", "names": ["Bruise", "contus", "BRUISE", "bruise", "Bruises", "bruises", "bruised", "Bruised", "BRUISING", "bruising", "Bruising", "Contused", "contused", "contusion", "CONTUSION", "Contusion", "CONTUSIONS", "Contusions", "contusions", "Contusion NOS", "Contused wound", "Contusion, NOS", "contused wound", "Bruise - lesion", "Wound, contused", "Contused Wounds", "Bruise/Contusion", "Contusion - lesion", "Contusion (disorder)", "contusion (physical finding)", "Contusion of unspecified site", "Contusion - lesion (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Contusions", "shortest_name_length": 6}
{"curie": "UMLS:C1304404", "names": ["Malignant Skin Vascular Tumor", "Malignant vascular tumor of skin", "skin malignant neoplasm vascular", "Malignant Skin Vascular Neoplasm", "Malignant vascular tumour of skin", "Malignant Cutaneous Vascular Tumor", "malignant vascular neoplasm of skin", "Malignant Cutaneous Vascular Neoplasm", "Malignant vascular tumor of skin (disorder)", "malignant vascular neoplasm of skin (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant vascular tumor of skin", "shortest_name_length": 29}
{"curie": "OMIM:611738", "names": ["BMND7", "BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 5}
{"curie": "UMLS:C1336390", "names": ["Stage IVB Pharynx Carcinoma", "Pharyngeal Cancer Stage IVB", "Stage IVB Pharyngeal Cancer", "Stage IVB Pharyngeal Carcinoma", "Stage IVB Carcinoma of Pharynx", "Stage IVB Carcinoma of the Pharynx"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Pharyngeal Carcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0015193", "names": ["HF", "fetal edema", "Fetal edema", "Fetal Edema", "Edema, Fetal", "Fetal hydrops", "Fetal Hydrops", "fetal hydrops", "hydrops fetal", "hydrops; fetal", "fetal anasarca", "Hydrops, Fetal", "Fetal anasarca", "HYDROPS FETALIS", "Hydrops fetalis", "fetalis hydrops", "Hydrops Fetalis", "hydrops fetalis", "hydrops foetalis", "Hydrops foetalis", "Hydrops fetalis NOS", "Hydrops fetalis, NOS", "HF - Hydrops fetalis", "Hydrops foetalis, NOS", "HF - Hydrops foetalis", "generalized fetal edema", "Generalized fetal edema", "hydrops fetalis (disease)", "hydrops fetalis nonimmune", "idiopathic hydrops fetalis", "Hydrops fetalis (disorder)", "familial non-immune hydrops fetalis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hydrops fetalis", "shortest_name_length": 2}
{"curie": "MONDO:0002067", "names": ["female breast upper-inner quadrant cancer", "malignant tumor of upper inner quadrant of female breast", "malignant neoplasm of upper inner quadrant of female breast", "malignant neoplasm of upper-inner quadrant of female breast", "Malignant neoplasm of upper-inner quadrant of female breast", "Malignant neoplasm of upper-inner quadrant of female breast (disorder)", "malignant neoplasm of upper inner quadrant of female breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "female breast upper-inner quadrant cancer", "shortest_name_length": 41}
{"curie": "UMLS:C1336458", "names": ["Stage I Immature Testicular Teratoma", "Stage I Immature Testicular Teratoma AJCC v6", "Stage I Immature Testicular Teratoma AJCC v7", "Stage I Immature Testicular Teratoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Immature Testicular Teratoma AJCC v6 and v7", "shortest_name_length": 36}
{"curie": "MONDO:0009193", "names": ["Epithelial Squamous Dysplasia, Keratinizing Desquamative, of Urinary Tract", "EPITHELIAL SQUAMOUS DYSPLASIA, KERATINIZING DESQUAMATIVE, OF URINARY TRACT", "epithelial squamous dysplasia, keratinizing desquamative, of urinary tract"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epithelial squamous dysplasia, keratinizing desquamative, of urinary tract", "shortest_name_length": 74}
{"curie": "UMLS:C0342579", "names": ["electrolyte disorder", "Electrolyte Imbalance", "Electrolyte imbalance", "ELECTROLYTE IMBALANCE", "electrolyte imbalance", "Imbalance;electrolyte", "disorders electrolyte", "electrolyte imbalances", "electrolytes imbalance", "imbalance; electrolyte", "disorders electrolytes", "electrolytes imbalances", "electrolyte disturbance", "disturbances electrolyte", "Electrolyte disturbances", "Electrolyte imbalance NOS", "Electrolyte imbalance, NOS", "electrolyte balance; abnormal", "abnormal; electrolyte balance", "disorder; balance, electrolyte", "balance; disorder, electrolyte", "electrolyte(balance); disorder", "Electrolyte imbalance (disorder)", "disturbance; balance, electrolyte"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Electrolyte imbalance", "shortest_name_length": 20}
{"curie": "MONDO:0009871", "names": ["HJDD", "pili torti and developmental delay", "Pili torti and developmental delay", "PILI TORTI AND DEVELOPMENTAL DELAY", "abnormal hair, joint laxity, and developmental delay", "ABNORMAL HAIR, JOINT LAXITY, AND DEVELOPMENTAL DELAY", "Pili torti developmental delay neurological abnormalities", "pili torti developmental delay neurological abnormalities", "pili torti-developmental delay-neurological abnormalities syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pili torti-developmental delay-neurological abnormalities syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0016616", "names": ["oligoarticular JIA without anti-nuclear antibodies", "pauciarticular chronic arthritis without anti-nuclear antibodies", "oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies", "shortest_name_length": 50}
{"curie": "MONDO:0013930", "names": ["CG6", "CGC", "CG4", "PBD4A", "peroxisome biogenesis disorder 4A", "Peroxisome Biogenesis Disorder 4A", "classic peroxisome biogenesis disorder", "peroxisome biogenesis disorder 4A (Zellweger)", "PEROXISOME BIOGENESIS DISORDER 4A (ZELLWEGER)", "peroxisome biogenesis disorder, complementation group 4", "Peroxisome Biogenesis Disorder, Complementation Group 4", "PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 6", "Peroxisome Biogenesis Disorder, Complementation Group C", "Peroxisome Biogenesis Disorder, Complementation Group 6", "PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP C", "PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 4", "peroxisome biogenesis disorder, complementation group C", "peroxisome biogenesis disorder, complementation group 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peroxisome biogenesis disorder 4A (Zellweger)", "shortest_name_length": 3}
{"curie": "MONDO:0007217", "names": ["BDA3", "brachymesophalangy V", "BRACHYMESOPHALANGY V", "Brachymesophalangy V", "Brachymesophalangy 5", "Brachydactyly type A3", "brachydactyly type A3", "Type A3 brachydactyly", "Brachymesophalangism V", "Brachydactyly, Type A3", "brachydactyly, type A3", "BRACHYDACTYLY, TYPE A3", "Brachydactyly-clinodactyly", "BRACHYDACTYLY-CLINODACTYLY", "brachydactyly-clinodactyly", "Brachymesophalangy V (finger)", "Brachydactyly type A3 (disorder)", "Fifth finger mid-phalanx hypoplasia", "Short middle bone of the pinky finger", "Short middle bone of the pinkie finger", "Short middle phalanx of the 5th finger", "Short middle bone of the little finger", "5th finger middle phalangeal hypoplasia", "Hypoplastic middle phalanx (5th finger)", "Hypoplastic fifth finger middle phalanx", "Short middle phalanx of the little finger", "Hypoplastic middle phalanx of the 5th finger", "Hypoplastic/small middle phalanx of the 5th finger", "Hypoplastic/small middle phalanx of the little finger"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brachydactyly type A3", "shortest_name_length": 4}
{"curie": "UMLS:C1328348", "names": ["Mitochondrial Hepatopathy", "Mitochondrial hepatopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mitochondrial hepatopathy", "shortest_name_length": 25}
{"curie": "MONDO:0008132", "names": ["OPTIC ATROPHY WITH DEMYELINATING DISEASE OF CNS", "Optic Atrophy with Demyelinating Disease of CNS", "optic atrophy with demyelinating disease of CNS", "Leber hereditary optic neuropathy with demyelinating disease of CNS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "optic atrophy with demyelinating disease of CNS", "shortest_name_length": 47}
{"curie": "MONDO:0005344", "names": ["HBV", "hepatitis B", "HEPATITIS B", "Hepatitis B", "hepatitis b", "serum hepatitis", "Serum hepatitis", "serum; hepatitis", "HEPATITIS, SERUM", "hepatitis; serum", "hepatitis type B", "b viral hepatitis", "viral Hepatitis B", "viral hepatitis b", "hepatitis viral b", "Viral Hepatitis B", "hepatitis b viral", "Viral hepatitis B", "hepatitis, B virus", "chronic hepatitis B", "SH - Serum hepatitis", "Hepatitis B infection", "Hepatitis B Infection", "hepatitis B infection", "Type B viral hepatitis", "Viral hepatitis type B", "Viral hepatitis, type B", "Hepatitis B virus (HBV)", "Viral serum hepatitis B", "hepatitis; virus, type, B", "virus; hepatitis, type, B", "Hepatitis B Virus Infection", "hepatitis B virus infection", "viral hepatitis B infection", "Hepatitis B Virus infection", "Hepatitis B virus hepatitis", "Viral hepatitis type B (disorder)", "hepatitis B infection (diagnosis)", "Hepatitis B virus caused hepatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hepatitis B virus infection", "shortest_name_length": 3}
{"curie": "UMLS:C0157266", "names": ["Second Stage Arrest", "Prolonged 2nd stage", "long; delivery, second stage", "labor; prolonged, second stage", "prolonged second stage of labor", "Arrest of Labor in Second Stage", "Prolonged second stage of labor", "Prolonged Second Stage of Labor", "Prolonged second stage of labour", "delivery; prolonged, second stage", "Prolonged second stage (of labor)", "prolonged; delivery, second stage", "Prolonged second stage (of labour)", "Prolonged second stage of labor (disorder)", "prolonged second stage of labor (diagnosis)", "labor; prolonged or protracted, second stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prolonged second stage of labor", "shortest_name_length": 19}
{"curie": "MONDO:0016978", "names": ["Poorly differentiated thymic neuroendocrine carcinoma", "poorly differentiated thymic neuroendocrine carcinoma", "Poorly-differentiated thymic neuroendocrine carcinoma", "Poorly-differentiated neuroendocrine carcinoma of thymus", "Poorly-differentiated neuroendocrine carcinoma of thymus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "poorly differentiated thymic neuroendocrine carcinoma", "shortest_name_length": 53}
{"curie": "UMLS:C5556696", "names": ["Refractory Medulloblastoma, WNT-Activated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Medulloblastoma, WNT-Activated", "shortest_name_length": 41}
{"curie": "UMLS:C5204114", "names": ["Early Stage Pancreatic Ductal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Early Stage Pancreatic Ductal Adenocarcinoma", "shortest_name_length": 44}
{"curie": "MONDO:0032586", "names": ["DIAR10", "DIARRHEA 10, PROTEIN-LOSING ENTEROPATHY TYPE", "diarrhea 10, protein-losing enteropathy type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diarrhea 10, protein-losing enteropathy type", "shortest_name_length": 6}
{"curie": "MONDO:0019392", "names": ["SCAP", "Syringadenoma", "papillary Syringadenoma", "Papillary Syringadenoma", "Papillary syringadenoma", "papillary syringadenoma", "syringadenoma; papillary", "papillary; syringadenoma", "Syringadenoma papilliferum", "Papillary Syringocystadenoma", "papillary syringocystadenoma", "Papillary syringocystadenoma", "papillary; syringocystadenoma", "Papillary Syringocystadenomas", "syringocystadenoma; papillary", "Syringocystadenoma, Papillary", "Syringocystadenoma Papilliferum", "Syringocystadenoma papilliferum", "syringocystadenoma papilliferum", "Syringocystadenoma Papilliferums", "Papilliferum, Syringocystadenoma", "Syringocystadenoma papilliferum (disorder)", "Nevus syringocystadenomatosus papilliferus", "Fistulous vegetative verrucous hydradenoma", "fistulous vegetative verrucous hydradenoma", "naevus syringocystadenomatosus papilliferus", "Naevus syringocystadenomatosus papilliferus", "papillary syringadenoma (morphologic abnormality)", "Papillary syringadenoma (morphologic abnormality)", "papillary Syringadenoma (syringocystadenoma papilliferum)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syringocystadenoma papilliferum", "shortest_name_length": 4}
{"curie": "MONDO:0007587", "names": ["RASMUSSEN SYNDROME", "Rasmussen syndrome", "Rasmussen-Johnsen-Thomsen syndrome", "Rasmussen Johnsen Thomsen syndrome", "external auditory canal atresia-vertical talus-hypertelorism syndrome", "External auditory canal atresia-vertical talus-hypertelorism syndrome", "External auditory canal atresia, vertical talus, hypertelorism syndrome", "External Auditory Canal, Bilateral Atresia Of, With Congenital Vertical Talus", "EXTERNAL AUDITORY CANAL, BILATERAL ATRESIA OF, WITH CONGENITAL VERTICAL TALUS", "external auditory canal, bilateral atresia of, with congenital vertical talus", "External auditory canal atresia, vertical talus, hypertelorism syndrome (disorder)", "inherited congenital bilateral atresia of the external auditory canal, congenital bilateral vertical talus and increased interocular distance", "Inherited congenital bilateral atresia of the external auditory canal, congenital bilateral vertical talus and increased interocular distance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "external auditory canal atresia-vertical talus-hypertelorism syndrome", "shortest_name_length": 18}
{"curie": "MONDO:0011588", "names": ["BDPLT12", "PGHS1 deficiency", "PGHS1 DEFICIENCY", "PGHS1 Deficiency", "platelet COX1 deficiency", "PLATELET COX1 DEFICIENCY", "Platelet Cox1 Deficiency", "platelet-type bleeding disorder 12", "Platelet Cyclooxygenase 1 Deficiency", "PLATELET CYCLOOXYGENASE 1 DEFICIENCY", "BLEEDING DISORDER, PLATELET-TYPE, 12", "platelet cyclooxygenase 1 deficiency", "bleeding disorder, platelet-type, 12", "platelet prostaglandin-endoperoxide synthase 1 deficiency", "Prostaglandin-Endoperoxide Synthase 1 Deficiency, Platelet", "PROSTAGLANDIN-ENDOPEROXIDE SYNTHASE 1 DEFICIENCY, PLATELET", "prostaglandin-endoperoxide synthase 1 deficiency, platelet"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "platelet-type bleeding disorder 12", "shortest_name_length": 7}
{"curie": "MONDO:0021718", "names": ["polyneuritis", "Polyneuritis", "POLYNEURITIS", "Polyneuritides", "Multiple neuritis", "Polyneuritis, NOS", "multiple neuritis", "Neuritis, Multiple", "neuritis; multiple", "multiple; neuritis", "Polyneuritis (disorder)", "inflammatory polyneuropathy", "Inflammatory polyneuropathy", "multiple peripheral neuritis", "neuritis; peripheral, multiple", "peripheral; neuritis, multiple"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyneuritis", "shortest_name_length": 12}
{"curie": "MONDO:0015326", "names": ["Hunter-Thompson-Reed syndrome", "Hunter Thompson Reed syndrome", "night blindness-skeletal anomalies-dysmorphism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "night blindness-skeletal anomalies-dysmorphism syndrome", "shortest_name_length": 29}
{"curie": "UMLS:C4527324", "names": ["Recurrent Gray Zone Lymphoma", "Recurrent B-Cell Lymphoma, Unclassifiable, with Features Intermediate between Diffuse Large B-Cell Lymphoma and Classic Hodgkin Lymphoma", "Recurrent B-Cell Lymphoma, Unclassifiable, with Features Intermediate between Diffuse Large B-Cell Lymphoma and Classical Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent B-Cell Lymphoma, Unclassifiable, with Features Intermediate between Diffuse Large B-Cell Lymphoma and Classic Hodgkin Lymphoma", "shortest_name_length": 28}
{"curie": "MONDO:0021082", "names": ["Meckel's diverticulum tumor", "Meckel diverticulum neoplasm", "tumor of Meckel's diverticulum", "Meckel's diverticulum neoplasm", "Tumor of Meckel's diverticulum", "Neoplasm of Meckel diverticulum", "Tumour of Meckel's diverticulum", "Neoplasm of Meckel's diverticulum", "neoplasm of Meckel's diverticulum", "Meckel's diverticulum neoplasm (disease)", "Neoplasm of Meckel's diverticulum (disorder)", "neoplasm of Meckel's diverticulum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meckel diverticulum neoplasm", "shortest_name_length": 27}
{"curie": "MONDO:0004312", "names": ["Suprasellar Meningioma", "suprasellar meningioma", "sella turcica meningioma (disease)", "meningioma (disease) of sella turcica"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "suprasellar meningioma", "shortest_name_length": 22}
{"curie": "MONDO:0013696", "names": ["SCZD17", "SCHIZOPHRENIA 17", "chromosome 2p16.3 deletion syndrome", "CHROMOSOME 2p16.3 DELETION SYNDROME", "chromosome 2P16.3 deletion syndrome", "schizophrenia, susceptibility to, 17"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 2p16.3 deletion syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C0393664", "names": ["multiple sclerosis acute relapsing", "Acute Relapsing Multiple Sclerosis", "Acute relapsing multiple sclerosis", "Multiple Sclerosis, Acute Relapsing", "Acute relapsing multiple sclerosis (disorder)", "Acute relapsing multiple sclerosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Multiple Sclerosis, Acute Relapsing", "shortest_name_length": 34}
{"curie": "MONDO:0008662", "names": ["VRCP", "MRCS2", "ADVIRC", "VRCP autosomal dominant", "VITREORETINOCHOROIDOPATHY", "Vitreoretinochoroidopathy", "vitreoretinochoroidopathy", "vitreoretinochoroidopathy dominant", "Vitreoretinochoroidopathy dominant", "Autosomal dominant vitreoretinochoroidopathy", "autosomal dominant vitreoretinochoroidopathy", "Autosomal dominant Vitreoretinochoroidopathy", "vitreoretinochoroidopathy, autosomal dominant", "VITREORETINOCHOROIDOPATHY, AUTOSOMAL DOMINANT", "Vitreoretinochoroidopathy, Autosomal Dominant", "Autosomal dominant vitreoretinochoroidopathy (disorder)", "Autosomal dominant vitreoretinochoroidopathy with nanophthalmos", "VITREORETINOCHOROIDOPATHY, AUTOSOMAL DOMINANT, WITH NANOPHTHALMOS", "Vitreoretinochoroidopathy, Autosomal Dominant, With Nanophthalmos", "Vitreoretinochoroidopathy with microcornea, glaucoma and cataract", "vitreoretinochoroidopathy, autosomal dominant, with nanophthalmos", "VITREORETINOCHOROIDOPATHY WITH MICROCORNEA, GLAUCOMA, AND CATARACT", "Vitreoretinochoroidopathy With Microcornea, Glaucoma, And Cataract", "vitreoretinochoroidopathy with microcornea, glaucoma, and cataract", "microcornea, Rod-cone dystrophy, cataract, and posterior staphyloma", "MICROCORNEA, ROD-CONE DYSTROPHY, CATARACT, AND POSTERIOR STAPHYLOMA 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant vitreoretinochoroidopathy", "shortest_name_length": 4}
{"curie": "UMLS:C0856053", "names": ["Leukemia secondary", "secondary leukemia", "Leukaemia secondary", "leukaemia secondary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leukaemia secondary", "shortest_name_length": 18}
{"curie": "MONDO:0043994", "names": ["Acute Cholecystitis", "CHOLECYSTITIS ACUTE", "acute cholecystitis", "Cholecystitis acute", "Acute cholecystitis", "Cholecystitis, Acute", "CHOLECYSTITIS, ACUTE", "acute; cholecystitis", "cholecystitis; acute", "Cholecystitis acute NOS", "Acute calculous cholecystitis", "Acute cholecystitis (disorder)", "acute cholecystitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute cholecystitis", "shortest_name_length": 19}
{"curie": "UMLS:C0876997", "names": ["Factor VIII inhibition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Factor VIII inhibition", "shortest_name_length": 22}
{"curie": "MONDO:0030935", "names": ["MC2DN2", "mitochondrial complex 2 deficiency, nuclear type 2", "MITOCHONDRIAL COMPLEX II DEFICIENCY, NUCLEAR TYPE 2", "mitochondrial complex II deficiency, nuclear type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 2 deficiency, nuclear type 2", "shortest_name_length": 6}
{"curie": "UMLS:C4048194", "names": ["Diffuse C-Cell Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse C-Cell Hyperplasia", "shortest_name_length": 26}
{"curie": "MONDO:0006886", "names": ["Carcinoma, Papillary, Follicular", "papillary and follicular carcinoma", "Papillary and Follicular Carcinoma", "Papillary and follicular carcinoma", "carcinoma; follicular with papillary", "carcinoma; papillary with follicular", "follicular; carcinoma, with papillary", "papillary; carcinoma, with follicular", "Papillary and Follicular Adenocarcinoma", "papillary and follicular adenocarcinoma", "Papillary carcinoma, follicular variant", "Papillary and follicular adenocarcinoma", "papillary; carcinoma, follicular variant", "Mixed papillary and follicular carcinoma", "carcinoma; papillary, follicular variant", "Papillary carcinoma - follicular variant", "adenocarcinoma; follicular with papillary", "follicular; adenocarcinoma with papillary", "papillary; adenocarcinoma with follicular", "adenocarcinoma; papillary with follicular", "papillary follicular thyroid adenocarcinoma", "Papillary adenocarcinoma, follicular variant", "adenocarcinoma; papillary, follicular variant", "Papillary adenocarcinoma - follicular variant", "papillary; adenocarcinoma, follicular variant", "thyroid gland papillary and follicular carcinoma", "Thyroid Gland Papillary and Follicular Carcinoma", "Papillary and follicular adenocarcinoma (morphologic abnormality)", "Papillary carcinoma, follicular variant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid gland papillary and follicular carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0015483", "names": ["TCS", "TCOF", "Berry syndrome", "berry syndrome", "Thomson complex", "Treacher Collins", "Zwahlen syndrome", "Franceschetti syndrome", "treacher collin syndrome", "Franceschetti's syndrome", "syndrome treacher collin", "mandibulofacial syndrome", "TREACHER COLLINS SYNDROME", "treacher collins syndrome", "syndrome treacher collins", "collins syndrome treacher", "Treacher-Collins Syndrome", "bilateral facial agenesis", "Treacher-Collins syndrome", "Treacher Collins Syndrome", "Treacher Collins syndrome", "MANDIBULOFACIAL DYSOSTOSIS", "treacher collins' syndrome", "collins syndrome treachers", "Mandibulofacial Dysostosis", "Treacher-Collins' syndrome", "Treacher Collins' syndrome", "Mandibulofacial dysostosis", "Mandibulofacial Dysostoses", "Syndrome, Treacher Collins", "mandibulofacial dysostosis", "mandibulofacial; dysostosis", "dysostosis; mandibulofacial", "Dysostosis, Mandibulofacial", "Dysostoses, Mandibulofacial", "Franceschetti-Klein syndrome", "dysostosis mandibulofacialis", "Franceschetti Klein syndrome", "Franceschetti-Zwahlen syndrome", "Treacher Collins syndrome (TCS)", "Berry-Treacher Collins syndrome", "mandibulofacial dysostosis (MFD)", "Mandibulofacial Dysostosis (MFD1)", "Mandibulofacial Dysostoses (MFD1)", "Dysostoses, Mandibulofacial (MFD1)", "Dysostosis, Mandibulofacial (MFD1)", "mandibulofacial dysostosis; syndrome", "Franceschetti Zwahlen Klein Syndrome", "Franceschetti-Zwahlen-Klein Syndrome", "Franceschetti-Zwahlen-Klein syndrome", "syndrome; mandibulofacial dysostosis", "Treacher Collins syndrome (disorder)", "Franceschetti-Zwahlen-Klein Syndromes", "Syndrome, Franceschetti-Zwahlen-Klein", "Syndromes, Franceschetti-Zwahlen-Klein", "mandibulofacial dysostosis (diagnosis)", "TREACHER COLLINS-FRANCESCHETTI SYNDROME", "Treacher Collins-Franceschetti syndrome", "Treacher Collins-Franceschetti Syndrome", "Treacher Collins Franceschetti Syndrome", "Treacher Collins-Franceschetti Syndromes", "Syndrome, Treacher Collins-Franceschetti", "Syndromes, Treacher Collins-Franceschetti", "Treacher Collins-Franceschetti (TCF) syndrome", "Bilateral and symmetric oto-mandibular dysplasia", "bilateral and symmetric oto-mandibular dysplasia", "Mandibulofacial dysostosis without limb anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mandibulofacial dysostosis", "shortest_name_length": 3}
{"curie": "UMLS:C0677659", "names": ["Peptic esophagitis", "reflux esophagitis", "Reflux esophagitis", "Peptic oesophagitis", "reflux oesophagitis", "Reflux oesophagitis", "esophagitis refluxing", "Esophageal reflux with esophagitis", "esophageal reflux with esophagitis", "Oesophageal reflux with oesophagitis", "gastroesophageal; reflux with esophagitis", "reflux; gastroesophageal, with esophagitis", "esophageal reflux with esophagitis (diagnosis)", "Gastroesophageal reflux disease with esophagitis", "Gastroesophageal reflux disease with oesophagitis", "Gastro-esophageal reflux disease with esophagitis", "Gastro-oesophageal reflux disease with oesophagitis", "Gastroesophageal reflux disease with esophagitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastro-esophageal reflux disease with esophagitis", "shortest_name_length": 18}
{"curie": "MONDO:0014666", "names": ["HLD11", "4H LEUKODYSTROPHY 3", "POLR1C leukodystrophy", "hypomyelinating leukodystrophy 11", "LEUKODYSTROPHY, HYPOMYELINATING, 11", "leukodystrophy, hypomyelinating, 11", "hypomyelinating leukodystrophy type 11", "leukodystrophy, hypomyelinating, type 11", "leukodystrophy caused by mutation in POLR1C"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypomyelinating leukodystrophy 11", "shortest_name_length": 5}
{"curie": "MONDO:0002100", "names": ["Cardiovascular Tumor", "Cardiovascular tumors", "cardiovascular cancer", "cardiovascular tumors", "Cardiovascular Tumors", "Tumors, Cardiovascular", "cardiovascular neoplasm", "Cardiovascular Neoplasm", "Neoplasm;cardiovascular", "Neoplasm cardiovascular", "Cardiovascular Neoplasms", "Neoplasms, Cardiovascular", "Neoplasm circulatory system", "cardiovascular system cancer", "Neoplasm of circulatory system", "cancer of cardiovascular system", "Malignant Cardiovascular Neoplasm", "malignant cardiovascular neoplasm", "Neoplasm of cardiovascular system", "neoplasm of the cardiovascular system", "malignant cardiovascular system neoplasm", "malignant neoplasm of cardiovascular system", "Neoplasm of cardiovascular system (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiovascular cancer", "shortest_name_length": 20}
{"curie": "MONDO:0005326", "names": ["Sunburn", "sunburn", "SUNBURN", "Sunburns", "Sunburn NOS", "sunburn; heat", "heat; sunburn", "Solar erythema", "solar erythema", "Solar Erythema", "Erythema solare", "Solar dermatitis", "solar dermatitis", "sunburn (diagnosis)", "Solar sensitiveness", "Burn(s);skin;sunburn", "Sunburn, unspecified", "Solar erythema (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sunburn", "shortest_name_length": 7}
{"curie": "MONDO:0007594", "names": ["Proaccelerin Excess", "PROACCELERIN EXCESS", "thrombophilia with elevated Factor 5", "THROMBOPHILIA WITH ELEVATED FACTOR V", "FACTOR V EXCESS WITH SPONTANEOUS THROMBOSIS", "factor V excess with spontaneous thrombosis", "Factor V Excess with Spontaneous Thrombosis", "factor 5 excess with spontaneous thrombosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "factor 5 excess with spontaneous thrombosis", "shortest_name_length": 19}
{"curie": "UMLS:C0272031", "names": ["Anemia due to Membrane Defect", "Anemia due to membrane defect", "Anaemia due to membrane defect", "Anemia due to membrane defect, NOS", "Anaemia due to membrane defect, NOS", "Hemolytic Anemia due to Membrane Defect", "Anemia due to membrane defect (disorder)", "Hemolytic Anemia due to Erythrocyte Membrane Defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anemia due to membrane defect", "shortest_name_length": 29}
{"curie": "UMLS:C4527415", "names": ["Luminal A Prostate Cancer", "Luminal A Prostate Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Luminal A Prostate Carcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0011677", "names": ["MEGARBANE SYNDROME", "Megarbane syndrome", "short stature, abnormal face, joint laxity, hernias, delayed bone age, and severe psychomotor retardation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Megarbane syndrome", "shortest_name_length": 18}
{"curie": "UMLS:C5243699", "names": ["Chronic graft versus host disease oral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic graft versus host disease oral", "shortest_name_length": 38}
{"curie": "MONDO:0014115", "names": ["HBSL", "aspartyl-tRNA synthetase deficiency", "ASPARTYL-tRNA SYNTHETASE DEFICIENCY", "HBSL - hypomyelination, brain stem, spinal cord, leg spasticity", "hypomyelination with brainstem and spinal cord involvement and leg spasticity", "HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEG SPASTICITY", "Hypomyelination with brain stem and spinal cord involvement and leg spasticity", "hypomyelination with brain stem and spinal cord involvement and leg spasticity", "Hypomyelination with brain stem and spinal cord involvement and leg spasticity (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypomyelination with brain stem and spinal cord involvement and leg spasticity", "shortest_name_length": 4}
{"curie": "MONDO:0001349", "names": ["Odontoclasia", "odontoclasia", "Odontoclasia (disorder)", "odontoclasia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "odontoclasia", "shortest_name_length": 12}
{"curie": "UMLS:C1167736", "names": ["Small Intestine Cancer Stage II", "Stage II Small Intestinal Cancer", "Small intestine carcinoma stage II", "Stage II Small Intestine Carcinoma", "Stage II Small Intestinal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small intestine carcinoma stage II", "shortest_name_length": 31}
{"curie": "MONDO:0012764", "names": ["RIDL", "Riddle Syndrome", "RIDDLE syndrome", "RIDDLE SYNDROME", "RNF168 deficiency", "RNF168 (ring finger protein 168) deficiency", "Radiosensitivity, Immunodeficiency, Dysmorphic Features, and Learning Difficulties", "radiosensitivity, immunodeficiency, dysmorphic features, and learning difficulties", "Radiosensitivity-immunodeficiency-dysmorphic features-learning difficulties syndrome", "radiosensitivity-immunodeficiency-dysmorphic features-learning difficulties syndrome", "Radiosensitivity, immunodeficiency, dysmorphic features, learning difficulties syndrome", "RADIOSENSITIVITY, IMMUNODEFICIENCY, DYSMORPHIC FACIAL FEATURES, AND LEARNING DIFFICULTIES", "RIDDLE (radiosensitivity, immunodeficiency, dysmorphic features, learning difficulties) syndrome", "Radiosensitivity, immunodeficiency, dysmorphic features, learning difficulties syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "RIDDLE syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0033818", "names": ["Terrien marginal degeneration", "Terrien's marginal degeneration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Terrien marginal degeneration", "shortest_name_length": 29}
{"curie": "UMLS:C4527011", "names": ["Stage IV Retroperitoneal Sarcoma", "Stage IV Retroperitoneal Sarcoma AJCC v8", "Stage IV Soft Tissue Retroperitoneal Sarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Retroperitoneal Sarcoma AJCC v8", "shortest_name_length": 32}
{"curie": "MONDO:0032662", "names": ["MRT67", "Mental Retardation, Autosomal Recessive 67", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 67", "autosomal recessive intellectual developmental disorder 67", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 67", "intellectual developmental disorder, autosomal recessive 67"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder, autosomal recessive 67", "shortest_name_length": 5}
{"curie": "UMLS:C5670625", "names": ["CNS Neuroblastoma, FOXR2-Activated", "Central Nervous System Neuroblastoma, FOXR2-Activated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Neuroblastoma, FOXR2-Activated", "shortest_name_length": 34}
{"curie": "UMLS:C3489728", "names": ["Familial intrahepatic cholestasis of pregnancy", "Familial recurrent intrahepatic cholestasis of pregnancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Familial intrahepatic cholestasis of pregnancy", "shortest_name_length": 46}
{"curie": "UMLS:C4525143", "names": ["Stage IVB Rectal Cancer", "Stage IVB Rectal Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Rectal Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "MONDO:0012640", "names": ["CMT4J", "Charcot-Marie-Tooth Disease Type 4J", "Charcot-Marie-Tooth disease type 4J", "CHARCOT-MARIE-TOOTH DISEASE, TYPE 4J", "Charcot-Marie-Tooth disease, type 4J", "Charcot-Marie-Tooth Disease, Type 4j", "FIG4 Charcot-Marie-Tooth disease type 4", "Charcot-Marie-Tooth disease type 4J (disorder)", "Charcot-Marie-Tooth disease type 4J (diagnosis)", "autosomal recessive Charcot-Marie-Tooth disease type 4J", "CHARCOT-MARIE-TOOTH DISEASE, AUTOSOMAL RECESSIVE, TYPE 4J", "Charcot-Marie-Tooth disease, autosomal recessive, type 4J", "Charcot-Marie-Tooth Disease, Autosomal Recessive, Type 4j", "Charcot-Marie-Tooth disease type 4 caused by mutation in FIG4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 4J", "shortest_name_length": 5}
{"curie": "UMLS:C0338375", "names": ["peritonitis aseptic", "Aseptic peritonitis", "aseptic peritonitis", "Sterile peritonitis", "aseptic; peritonitis", "peritonitis; aseptic", "Aseptic peritonitis (disorder)", "aseptic peritonitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aseptic peritonitis", "shortest_name_length": 19}
{"curie": "MONDO:0004374", "names": ["extraskeletal osteosarcoma", "Extraskeletal Osteosarcoma", "Adult Extraosseous Osteosarcoma", "adult extraosseous osteosarcoma", "adult extraskeletal osteosarcoma", "Adult Extraskeletal Osteosarcoma", "extraskeletal osteosarcoma, adult", "osteosarcoma, adult extraskeletal", "extraosseous osteosarcoma of adults"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult extraskeletal osteosarcoma", "shortest_name_length": 26}
{"curie": "MONDO:0023699", "names": ["Maroteaux Fonfria syndrome", "Apparent Apert syndrome with polydactyly", "apparent apert syndrome with polydactyly", "apert syndrome with polydactyly of hands and feet", "Apert syndrome with polydactyly of hands and feet"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Maroteaux Fonfria syndrome", "shortest_name_length": 26}
{"curie": "UMLS:C1880168", "names": ["Congenital Platelets Abnormality"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Platelets Abnormality", "shortest_name_length": 32}
{"curie": "MONDO:0011693", "names": ["NPG", "NTG", "GLAUCOMA, NORMAL TENSION, SUSCEPTIBILITY TO", "glaucoma, normal tension, susceptibility to", "glaucoma, normal pressure, susceptibility to", "GLAUCOMA, NORMAL PRESSURE, SUSCEPTIBILITY TO", "GLAUCOMA, NORMAL TENSION, SUSCEPTIBILITY TO (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glaucoma, normal tension, susceptibility to", "shortest_name_length": 3}
{"curie": "MONDO:0004792", "names": ["isthmus cancer", "Malignant neoplasm of isthmus", "isthmus of fallopian tube cancer", "cancer of isthmus of fallopian tube", "malignant isthmus of fallopian tube neoplasm", "malignant neoplasm of isthmus of fallopian tube"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cancer of isthmus of fallopian tube", "shortest_name_length": 14}
{"curie": "MONDO:0005063", "names": ["Medullary Breast Cancer", "medullary breast cancer", "breast medullary carcinoma", "medullary breast carcinoma", "breast carcinoma medullary", "Breast Medullary Carcinoma", "Medullary Breast Carcinoma", "medullary carcinoma breast", "medullary carcinoma of breast", "Medullary carcinoma of breast", "Medullary Carcinoma of Breast", "Medullary Carcinoma of the Breast", "medullary carcinoma of the breast", "invasive medullary breast carcinoma", "Invasive Medullary Breast Carcinoma", "Invasive Medullary Carcinoma of Breast", "invasive medullary carcinoma of breast", "Medullary carcinoma with lymphoid stroma", "medullary carcinoma of breast (diagnosis)", "Invasive Medullary Carcinoma of the Breast", "Infiltrating Medullary Carcinoma of Breast", "infiltrating medullary carcinoma of breast", "invasive medullary carcinoma of the breast", "infiltrating medullary carcinoma of the breast", "Infiltrating Medullary Carcinoma of the Breast", "Medullary breast carcinoma with lymphoid Stroma", "Medullary Breast Carcinoma with Lymphoid Stroma", "medullary breast carcinoma with lymphoid Stroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "medullary breast carcinoma", "shortest_name_length": 23}
{"curie": "UMLS:C0036494", "names": ["MAL DE MER", "mal de mer", "Seasickness", "seasickness", "Sea sickness", "SEA SICKNESS", "Sea Sickness", "sea sickness", "Sickness, Sea", "sea sickness; nausea", "Sea sickness symptom", "nausea; sea sickness", "Sea sickness (finding)", "seasickness (diagnosis)", "disease (or disorder); sea sickness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Seasickness", "shortest_name_length": 10}
{"curie": "UMLS:C0270221", "names": ["IDM", "Infant of Diabetic Mother", "maternal diabetes syndrome", "infant; of diabetic mother", "Maternal diabetes syndrome", "diabetes; mother (infant of)", "diabetic infant mother syndrome", "infant; diabetes, mother, syndrome", "syndrome; infant of diabetic mother", "Infant of a diabetic mother syndrome", "Syndrome of Infant of Diabetic Mother", "Syndrome of infant of diabetic mother", "Syndrome of infant of a diabetic mother", "Syndrome of \"infant of a diabetic mother\"", "Syndrome of infant of diabetic mother (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Syndrome of infant of diabetic mother", "shortest_name_length": 3}
{"curie": "UMLS:C1706833", "names": ["Appendix Small Cell Carcinoma", "small cell carcinoma of appendix", "small cell carcinoma of appendix (diagnosis)", "Appendix Small Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small cell carcinoma of appendix", "shortest_name_length": 29}
{"curie": "UMLS:C4520897", "names": ["Stage IV Lentigo Maligna", "Stage IV Lentigo Maligna Melanoma", "Stage IV Lentigo Maligna Melanoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Lentigo Maligna Melanoma AJCC v6 and v7", "shortest_name_length": 24}
{"curie": "MONDO:0043009", "names": ["genetic lethal multiple congenital anomalies/dysmorphic syndrome", "hereditary lethal multiple congenital anomalies/dysmorphic syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genetic lethal multiple congenital anomalies/dysmorphic syndrome", "shortest_name_length": 64}
{"curie": "MONDO:0003959", "names": ["Breast Large Cell Neuroendocrine Carcinoma", "breast large cell neuroendocrine carcinoma", "large cell neuroendocrine carcinoma of breast", "large cell neuroendocrine carcinoma of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast large cell neuroendocrine carcinoma", "shortest_name_length": 42}
{"curie": "UMLS:C5670669", "names": ["Stage IA Cervical Cancer FIGO 2009", "Stage IA Cervical Carcinoma FIGO 2009"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Cervical Cancer FIGO 2009", "shortest_name_length": 34}
{"curie": "UMLS:C5446589", "names": ["Unresectable Small Intestinal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Small Intestinal Adenocarcinoma", "shortest_name_length": 44}
{"curie": "UMLS:C0398776", "names": ["HAE 2", "HAE-II", "Hereditary angioedema type 2", "Hereditary angioedema - type 2", "Hereditary angio-edema - type 2", "Hereditary angio-oedema - type 2", "Hereditary C1 esterase inactivity", "Hereditary angioneurotic edema type 2", "Hereditary angioneurotic edema - type 2", "Hereditary angioneurotic oedema - type 2", "C1 esterase inhibitor deficiency - type 2", "c1 inhibitor deficiency - dysfunctional factor", "hereditary C1 inhibitor deficiency - dysfunctional factor", "Hereditary C1 esterase inhibitor deficiency - dysfunctional factor", "hereditary C1 inhibitor deficiency - dysfunctional factor (diagnosis)", "Hereditary C1 esterase inhibitor deficiency - dysfunctional factor (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hereditary C1 esterase inhibitor deficiency - dysfunctional factor", "shortest_name_length": 5}
{"curie": "MONDO:0009458", "names": ["SIOD", "Schimke syndrome", "Schimke Immunoosseous dysplasia", "Schimke immunoosseous dysplasia", "Schimke IMMUNOOSSEOUS dysplasia", "Schimke Immunoosseous Dysplasia", "SCHIMKE IMMUNOOSSEOUS DYSPLASIA", "Schimke Immuno-Osseous Dysplasia", "Schimke immuno-osseous dysplasia", "Immunoosseous dysplasia Schimke type", "immunoosseous dysplasia Schimke type", "IMMUNOOSSEOUS dysplasia, Schimke type", "IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE", "Immunoosseous Dysplasia, Schimke Type", "Schimke immuno-osseous dysplasia (disorder)", "spondyloepiphyseal dysplasia nephrotic syndrome", "Spondyloepiphyseal dysplasia-nephrotic syndrome", "spondyloepiphyseal dysplasia-nephrotic syndrome", "spondyloepiphyseal dysplasia - nephrotic syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Schimke immuno-osseous dysplasia", "shortest_name_length": 4}
{"curie": "MONDO:0030877", "names": ["CAFD2", "cardioacrofacial dysplasia 2", "CARDIOACROFACIAL DYSPLASIA 2", "cardioacrofacial dysplasia 2, autosomal dominant, somatic mosaicism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardioacrofacial dysplasia 2", "shortest_name_length": 5}
{"curie": "MONDO:0100068", "names": ["SLC10A7-CDG", "SLC10A7 deficiency", "SLC10A7-congenital disorder of glycosylation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SLC10A7-congenital disorder of glycosylation", "shortest_name_length": 11}
{"curie": "MONDO:0001930", "names": ["acute cholangitis", "Acute Cholangitis", "Acute cholangitis", "Cholangitis acute", "cholangitis, acute", "Cholangitis acute NOS", "Acute cholangitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute cholangitis", "shortest_name_length": 17}
{"curie": "MONDO:0021189", "names": ["intestinal motility disease", "disorder of intestinal motility"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intestinal motility disease", "shortest_name_length": 27}
{"curie": "UMLS:C1299433", "names": ["Left Main Disease", "Left Main Diseases", "Left Main Coronary Disease", "Left Main Coronary Artery Disease", "coronary artery disease left main", "Left main coronary artery disease", "Left main coronary artery disease (disorder)", "Left main coronary artery disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Left Main Coronary Artery Disease", "shortest_name_length": 17}
{"curie": "MONDO:0015087", "names": ["autosomal dominant complex HSP", "autosomal dominant complex SPG", "autosomal dominant complicated HSP", "autosomal dominant complicated SPG", "autosomal dominant complex spastic paraplegia", "autosomal dominant complicated spastic paraplegia", "autosomal dominant complex hereditary spastic paraplegia", "complex hereditary spastic paraplegia, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant complex spastic paraplegia", "shortest_name_length": 30}
{"curie": "UMLS:C4763790", "names": ["Refractory Lymphoproliferative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Lymphoproliferative Disorder", "shortest_name_length": 39}
{"curie": "MONDO:0006981", "names": ["ie", "sbe", "SBE", "Endocarditis Lenta", "Endocarditis lenta", "endocarditis lenta", "lenta; endocarditis", "endocarditis; lenta", "Endocarditis, lenta", "ENDOCARDITIS INFECTIOUS", "infectious endocarditis", "endocarditis infectious", "infectious; endocarditis", "Subacute endocarditis, lenta", "Subacute bacterial endocarditi", "bacterial endocarditis subacute", "ENDOCARDITIS BACTERIAL SUBACUTE", "Subacute bacterial endocarditis", "Subacute Bacterial Endocarditis", "subacute bacterial endocarditis", "Subacute endocarditis, bacterial", "Endocarditis, Subacute Bacterial", "Bacterial Endocarditis, Subacute", "Bacterial endocarditis, subacute", "Subacute Bacterial Endocarditides", "ENDOCARDITIS, BACTERIAL, SUBACUTE", "BACTERIAL ENDOCARDITIS (SUBACUTE)", "Endocarditides, Subacute Bacterial", "Bacterial Endocarditides, Subacute", "SBE - Subacute bacterial endocarditis", "SBE (subacute bacterial endocarditis)", "Subacute bacterial endocarditis (disorder)", "subacute bacterial endocarditis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subacute bacterial endocarditis", "shortest_name_length": 2}
{"curie": "UMLS:C0266791", "names": ["True knot in cord", "Knot in fetal cord", "Umbilical Cord True Knot", "Umbilical cord, true knot", "true knot of umbilical cord", "True knot in umbilical cord", "True knot of umbilical cord", "Knot in cord with compression", "Knot in fetal cord with compression", "True knot of umbilical cord (disorder)", "true knot of umbilical cord (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "True knot of umbilical cord", "shortest_name_length": 17}
{"curie": "MONDO:0017053", "names": ["intermittent MSUD", "intermittent BCKD deficiency", "intermittent maple syrup urine disease", "intermittent branched-chain 2-ketoacid dehydrogenase deficiency", "intermittent branched-chain alpha-ketoacid dehydrogenase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intermittent maple syrup urine disease", "shortest_name_length": 17}
{"curie": "UMLS:C0403688", "names": ["prostate injury", "Prostatic Injury", "injury; prostate", "prostate; injury", "Injury of prostate", "Injury of Prostate", "injury of prostate", "Injury of prostate (disorder)", "injury of prostate (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of prostate", "shortest_name_length": 15}
{"curie": "MONDO:0000967", "names": ["conventional lipoma", "Conventional Lipoma", "Classic Type Lipoma", "classic type lipoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "conventional lipoma", "shortest_name_length": 19}
{"curie": "MONDO:0019404", "names": ["Perineurioma", "perineurioma", "Perineuriomas", "Perineurioma, NOS", "Perineurioma (disorder)", "Soft Tissue Perineurioma", "Soft tissue perineurioma", "soft tissue perineurioma", "soft tissue Perineurioma", "Soft Tissue Perineurioma (WHO Grades I, II, or III)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "perineurioma", "shortest_name_length": 12}
{"curie": "MONDO:0008814", "names": ["argininemia", "ARGININEMIA", "Argininemia", "Argininaemia", "argininaemia", "ARG1 DEFICIENCY", "ARGI deficiency", "ARG1 Deficiency", "Arg1 deficiency", "hyperargininemia", "Hyperargininemia", "HYPERARGININEMIA", "Deficiency, ARG1", "Hyperargininemias", "Hyperargininaemia", "ARG1 Deficiencies", "hyperargininaemia", "Deficiencies, ARG1", "Arginase Deficiency", "ARGINASE DEFICIENCY", "arginase deficiency", "Arginase deficiency", "Deficiency, Arginase", "Arginase 1 deficiency", "Arginase Deficiencies", "Deficiency of arginase", "Deficiencies, Arginase", "argininemia (diagnosis)", "deficiency of canavanase", "Arginase Deficiency Disease", "Arginase Deficiency Diseases", "Deficiency Disease, Arginase", "Deficiency Diseases, Arginase", "Arginase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperargininemia", "shortest_name_length": 11}
{"curie": "MONDO:0016889", "names": ["monosomy 7p", "7p deletion", "deletion 7p", "7p monosomy", "partial monosomy 7p", "chromosome 7p deletion", "partial deletion of chromosome 7p", "partial monosomy of chromosome 7p", "partial monosomy of the short arm of chromosome 7", "partial deletion of the short arm of chromosome 7", "partial deletion of the short arm of chromosome type 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of the short arm of chromosome 7", "shortest_name_length": 11}
{"curie": "MONDO:0006721", "names": ["de Quervain disease", "De Quervain disease", "De Quervain Disease", "de quervain disease", "de quervains disease", "de Quervain; disease", "Disease;De Quervains", "De Quervains disease", "De Quervains Disease", "Disease, De Quervain", "disease; de Quervain", "de disease quervain's", "de Quervain's disease", "De Quervain's disease", "De Quervain's Disease", "quervain's de disease", "de quervain's disease", "DE QUERVAIN'S DISEASE", "Tenosynovitis stenosans", "tenosynovitis stenosans", "stenosans; tenosynovitis", "tenosynovitis; stenosans", "tenosynovitis de quervain", "de quervain tenosynovitis", "TENOSYNOVITIS, DE QUERVAIN", "de quervains tenosynovitis", "de quervain's tenosynovitis", "de Quervain's tenosynovitis", "De Quervain's tenosynovitis", "Radial styloid tenosynovitis", "Tenosynovitis, de Quervain's", "tenosynovitis, de Quervain's", "radial styloid tenosynovitis", "De Quervain Stenosing Tenosynovitis", "Stenosing Tenosynovitis, De Quervain", "tenosynovitis; radial styloid process", "process; radial styloid, tenosynovitis", "de Quervain's tenosynovitis (diagnosis)", "Radial styloid tenosynovitis (disorder)", "Radial styloid tenosynovitis [de Quervain]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "de Quervain disease", "shortest_name_length": 19}
{"curie": "UMLS:C0262469", "names": ["Embolic stroke", "Embolic Stroke", "embolic stroke", "EMBOLIC STROKE", "Embolic Strokes", "Stroke, Embolic", "Strokes, Embolic", "embolic; apoplexy", "apoplexy; embolic", "APOPLEXY, EMBOLIC", "ischemic embolic stroke", "Embolic stroke (disorder)", "ischemic embolic stroke (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Embolic Stroke", "shortest_name_length": 14}
{"curie": "MONDO:0011230", "names": ["OPLL", "Posterior Longitudinal Ligament Ossification", "Posterior Longitudinal Ligament Calcification", "Posterior longitudinal ligament calcification", "posterior longitudinal ligament; ossification", "Ossification of posterior longitudinal ligament", "ossification of Posterior longitudinal ligament", "Ossification of Posterior Longitudinal Ligament", "Calcification of Posterior Longitudinal Ligament", "Ossification of posterior longitudinal ligament NOS", "Ossification of the posterior longitudinal ligament", "Ossification of posterior longitudinal ligament, NOS", "ossification; ligament, ligament, posterior longitudinal", "Ossification of posterior longitudinal ligament (disorder)", "ossification of the POSTERIOR longitudinal ligament of spine", "Ossification of the Posterior Longitudinal Ligament of Spine", "OSSIFICATION OF THE POSTERIOR LONGITUDINAL LIGAMENT OF SPINE", "ossification of the posterior longitudinal ligament of spine", "ossification of the posterior longitudinal ligament of the spine", "Ossification of the posterior longitudinal ligament of the spine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ossification of the posterior longitudinal ligament of the spine", "shortest_name_length": 4}
{"curie": "UMLS:C5419776", "names": ["Midgut Neuroendocrine Tumor G3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Midgut Neuroendocrine Tumor G3", "shortest_name_length": 30}
{"curie": "UMLS:C3274281", "names": ["TAPVR Type IV", "Type IV Total Anomalous Pulmonary Venous Return", "Type IV (Mixed) Total Anomalous Pulmonary Venous Return", "Total Anomalous Pulmonary Venous Return, Type IV (Mixed)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Type IV Total Anomalous Pulmonary Venous Return", "shortest_name_length": 13}
{"curie": "MONDO:0021102", "names": ["prostate phyllodes tumor", "Prostate Phyllodes Tumor", "phyllodes tumor of prostate", "prostate phyllodes neoplasm", "Prostate Phyllodes Neoplasm", "Phyllodes Tumor of Prostate", "phyllodes neoplasm of prostate", "prostate gland phyllodes tumor", "Phyllodes Neoplasm of Prostate", "phyllodes tumor of the prostate", "prostate cystosarcoma phyllodes", "Phyllodes Tumor of the Prostate", "Phyllodes tumor of the prostate", "Prostate Cystosarcoma Phyllodes", "Phyllodes Neoplasm of the Prostate", "Cystosarcoma Phyllodes of Prostate", "phyllodes neoplasm of the prostate", "cystosarcoma phyllodes of prostate", "Cystosarcoma phyllodes of the prostate", "cystosarcoma phyllodes of the prostate", "Cystosarcoma Phyllodes of the Prostate", "malignant phyllodes tumor of prostate (subtype)", "Phyllodes type of atypical prostatic hyperplasia", "Cystic epithelial-stromal tumors of the prostate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate phyllodes tumor", "shortest_name_length": 24}
{"curie": "MONDO:0002457", "names": ["TCS", "TCOF", "MFD1", "Franceschetti-Klein", "Franceschetti syndrome", "Treacher Collins syndrome", "Treacher-Collins syndrome", "Treacher Collins Syndrome", "mandibulofacial dysostosis", "Mandibulofacial Dysostosis", "Franceschetti-Klein syndrome", "complete mandibulofacial dysostosis", "complete mandibulofacial dysostosis (diagnosis)", "mandibulofacial dysostosis without limb anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Treacher-Collins syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0013713", "names": ["susceptibility to dengue virus", "DENGUE FEVER, SUSCEPTIBILITY TO", "dengue virus, susceptibility to", "Dengue fever, susceptibility to", "DENGUE VIRUS, SUSCEPTIBILITY TO", "DENGUE FEVER, PROTECTION AGAINST", "Dengue fever, protection against", "DENGUE SHOCK SYNDROME, SUSCEPTIBILITY TO", "Dengue shock syndrome, susceptibility to", "DENGUE HEMORRHAGIC FEVER, SUSCEPTIBILITY TO", "Dengue hemorrhagic fever, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dengue virus, susceptibility to", "shortest_name_length": 30}
{"curie": "UMLS:C0027686", "names": ["neovascularity", "Neovascularity", "neovascularized", "neoangiogenesis", "Neovascularized", "vascularization", "Vascularisation", "vascularisation", "Vascularization", "Neoangiogenesis", "NEOVASCULARISATION", "Neovascularisation", "Neovascularization", "neovascularization", "NEOVASCULARIZATION", "neovascularisation", "Pathologic Angiogenesis", "Angiogenesis, Pathologic", "Pathological Angiogenesis", "Angiogenesis, Pathological", "Pathologic Neovascularization", "Neovascularization, Pathologic", "Pathological Neovascularization", "Neovascularization, Pathological", "Neovascularization (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Neovascularization", "shortest_name_length": 14}
{"curie": "UMLS:C4688414", "names": ["Stage IA Vaginal Cancer", "Stage IA Vaginal Cancer AJCC v8", "Stage IA Vaginal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Vaginal Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "UMLS:C0272195", "names": ["Eosinopenia", "eosinopenia", "Eosinopenia (disorder)", "Eosinophilic cytopenia", "Eosinophilic leukopenia", "eosinopenia (diagnosis)", "eosinophilic leukopenia", "Disorder characterized by eosinopenia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eosinopenia", "shortest_name_length": 11}
{"curie": "MONDO:0014588", "names": ["CMS1E", "CMS11", "Cms Ie", "CMS Ie", "CMS1E, FORMERLY", "Cms Ie, formerly", "CMS Ie, FORMERLY", "congenital myasthenic syndrome 1e", "congenital myasthenic syndrome 11", "Myasthenic Syndrome, Congenital, Ie", "myasthenic syndrome, congenital, Ie", "MYASTHENIC SYNDROME, CONGENITAL, Ie", "RAPSN congenital myasthenic syndrome", "congenital myasthenic syndrome type 11", "MYASTHENIC SYNDROME, CONGENITAL, Ie, FORMERLY", "myasthenic syndrome, congenital, Ie, formerly", "congenital myasthenic syndrome caused by mutation in RAPSN", "congenital myasthenic syndrome 11 associated with acetylcholine receptor deficiency", "myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency", "Myasthenic Syndrome, Congenital, 11, Associated with Acetylcholine Receptor Deficiency", "MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myasthenic syndrome 11", "shortest_name_length": 5}
{"curie": "UMLS:C1112192", "names": ["Erythrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Erythrosis", "shortest_name_length": 10}
{"curie": "UMLS:C4521633", "names": ["Stage IV Laryngeal Throat Cancer", "Stage IV Laryngeal Cancer AJCC v8", "Stage IV Laryngeal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Laryngeal Cancer AJCC v8", "shortest_name_length": 32}
{"curie": "MONDO:0008019", "names": ["WNT4 deficiency", "WNT4 Deficiency", "Mullerian aplasia and hyperandrogenism", "Mullerian Aplasia and Hyperandrogenism", "MULLERIAN APLASIA AND HYPERANDROGENISM", "Müllerian aplasia and hyperandrogenism", "mullerian aplasia and hyperandrogenism", "Mullerian duct failure and hyperandrogenism", "Müllerian duct failure and hyperandrogenism", "MULLERIAN DUCT FAILURE AND HYPERANDROGENISM", "Mullerian Duct Failure and Hyperandrogenism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mullerian aplasia and hyperandrogenism", "shortest_name_length": 15}
{"curie": "MONDO:0017202", "names": ["Acute endophthalmitis", "acute endophthalmitis", "endophthalmitis, acute", "Acute endophthalmitis (disorder)", "acute endophthalmitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute endophthalmitis", "shortest_name_length": 21}
{"curie": "MONDO:0004696", "names": ["stage 0 larynx cancer", "larynx cancer, stage 0", "Larynx Carcinoma in situ", "Stage 0 Laryngeal Cancer", "Stage 0 Larynx Carcinoma", "laryngeal cancer stage 0", "stage 0 larynx carcinoma", "larynx in situ carcinoma", "Laryngeal cancer stage 0", "larynx carcinoma in situ", "Laryngeal Cancer Stage 0", "stage 0 laryngeal cancer", "Cancer in situ of larynx", "laryngeal cancer, stage 0", "Carcinoma in situ of larynx", "carcinoma in situ of larynx", "stage 0 carcinoma of larynx", "Laryngeal carcinoma in situ", "stage 0 laryngeal carcinoma", "LARYNGEAL CARCINOMA IN SITU", "Laryngeal Carcinoma Stage 0", "laryngeal carcinoma in situ", "Stage 0 Laryngeal Carcinoma", "Carcinoma in situ of Larynx", "laryngeal carcinoma stage 0", "Laryngeal Carcinoma in situ", "Stage 0 Carcinoma of Larynx", "stage 0 laryngeal throat cancer", "Laryngeal carcinoma in situ NOS", "stage 0 carcinoma of the larynx", "carcinoma in situ of the larynx", "stage 0 carcinoma of the Larynx", "Carcinoma in situ of the Larynx", "Stage 0 Carcinoma of the Larynx", "Stage 0 Laryngeal Throat Cancer", "stage 0 laryngeal cancer aJCC v7", "Carcinoma in situ of larynx, NOS", "stage 0 laryngeal cancer aJCC v8", "Stage 0 Laryngeal Cancer AJCC v8", "Stage 0 Laryngeal Cancer AJCC v7", "stage 0 laryngeal cancer aJCC v6", "Stage 0 Laryngeal Cancer AJCC v6", "stage 0 laryngeal carcinoma in situ", "Carcinoma in situ of larynx (disorder)", "carcinoma in situ of larynx (diagnosis)", "Stage 0 Laryngeal Cancer AJCC v6, v7, and V8", "stage 0 laryngeal cancer aJCC v6, v7, and V8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "larynx carcinoma in situ", "shortest_name_length": 21}
{"curie": "UMLS:C1695895", "names": ["Angiodermatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Angiodermatitis", "shortest_name_length": 15}
{"curie": "UMLS:C5419972", "names": ["Digestive System Leiomyoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Digestive System Leiomyoma", "shortest_name_length": 26}
{"curie": "MONDO:0006586", "names": ["dermatitis ficta", "Dermatitis ficta", "Feigned dermatitis", "Dermatitis simulata", "dermatitis factitia", "Dermatitis factitia", "factitia; dermatitis", "Dermatitis;factitial", "Factitial dermatitis", "factitial dermatitis", "dermatitis artifacta", "dermatitis artefacta", "DERMATITIS ARTEFACTA", "Neurotic excoriation", "neurotic excoriation", "Dermatitis artefacta", "dermatitis; factitia", "Dermatitis artifacta", "Simulated dermatitis", "Excoriation, neurotic", "neurotic; excoriation", "dermatitis; artefacta", "excoriation; neurosis", "excoriations neurotic", "artefacta; dermatitis", "DERMATITIS, FACTITIAL", "EXCORIATION, NEUROTIC", "neurosis; excoriation", "Factitious dermatitis", "excoriation; neurotic", "FACTITIONAL DERMATITIS", "factitious skin disease", "Factitious skin disease", "DA - Dermatitis artefacta", "Dermatitis factitia [artefacta]", "dermatitis factitia [artefacta]", "Dermatitis factitia (artefacta)", "dermatitis factitia (diagnosis)", "neurotic excoriation (diagnosis)", "Factitious skin disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurotic excoriation", "shortest_name_length": 16}
{"curie": "MONDO:0006938", "names": ["pyelitis", "PYELITIS", "Pyelitis", "Pyelitis NOS", "Pyelitis, NOS", "Pyelitis (disorder)", "pyelitis (diagnosis)", "renal pelvis inflammation", "inflammation of renal pelvis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyelitis", "shortest_name_length": 8}
{"curie": "MONDO:0011590", "names": ["anisomastia", "ANISOMASTIA", "Anisomastia", "Breast asymmetry", "Asymmetry of the breasts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anisomastia", "shortest_name_length": 11}
{"curie": "UMLS:C4521619", "names": ["Stage III Bone Cancer", "Stage III Bone Cancer AJCC v8", "Stage III Appendicular Skeleton, Trunk, Skull, and Facial Bones Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Bone Cancer AJCC v8", "shortest_name_length": 21}
{"curie": "MONDO:0019290", "names": ["Leukoderma", "leucoderma", "Leucoderma", "leukoderma", "leucodermas", "Achromoderma", "Hypomelanoses", "hypomelanoses", "Hypomelanosis", "hypomelanosis", "Depigmentation", "depigmentation", "HYPOPIGMENTATION", "skin hypopigment", "hypopigmentation", "Pigment Dilution", "Hypopigmentation", "Skin depigmented", "hypopigmented skin", "Hypopigmented skin", "Skin hypopigmented", "Hypopigmentation, NOS", "skin hypopigmentation", "Skin Hypopigmentation", "hypopigmentation skin", "Skin hypopigmentation", "Patchy lightened skin", "Hypopigmentation of skin", "Hypopigmentation disorder", "Hypopigmentation disorders", "Hypopigmentation of the skin", "hypopigmentation of the skin", "Hypopigmentation of skin, NOS", "Hypopigmentation of skin (disorder)", "hypopigmentation of the skin (disease)", "skin hypopigmentation (physical finding)", "Depigmentation (morphologic abnormality)", "Hypopigmentation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypopigmentation of the skin", "shortest_name_length": 10}
{"curie": "UMLS:C0234482", "names": ["Semantic Aphasia", "Semantic aphasia", "Semantic Aphasias", "Aphasia, semantic", "Aphasia, Semantic", "Semantic dysphasia", "Semantic aphasia (finding)", "Semantic dysphasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aphasia, Semantic", "shortest_name_length": 16}
{"curie": "MONDO:0020521", "names": ["EDS VIIA", "Ehlers-Danlos syndrome type 7A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ehlers-Danlos syndrome type 7A", "shortest_name_length": 8}
{"curie": "UMLS:C0150045", "names": ["Urge Incontinence", "Urge incontinence", "incontinence urge", "urge incontinence", "Incontinence, Urge", "incontinence; urge", "urge; incontinence", "urinary urge incontinence", "Urge Urinary Incontinence", "urine; incontinence, urge", "URINARY INCONTINENCE URGE", "Urinary urge incontinence", "urge urinary incontinence", "Urinary Urge Incontinence", "Urge urinary incontinence", "Urge incontinence of urine", "Urge incontinence syndrome", "Urge Incontinence Of Urine", "Urinary Incontinence, Urge", "urge incontinence of urine", "Urinary Reflex Incontinence", "incontinence; urinary, urge", "Incontinence, Urinary Reflex", "Must urinate at once with urge", "RNDx urge urinary incontinence", "Urge incontinence of urine (finding)", "urge incontinence of urine (diagnosis)", "Lack of bladder control if desire urgent", "Lack of bladder control if desire resisted", "RNDx urge urinary incontinence (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urge Incontinence", "shortest_name_length": 17}
{"curie": "MONDO:0004855", "names": ["tenosynovitis", "tenovaginitis", "Tenovaginitis", "Tenosynovitis", "TENOSYNOVITIS", "Peritendinitis", "Tendovaginitis", "tendovaginitis", "peritendinitis", "Tenosynovitides", "Tenontolemmitis", "Tenosynovitis NOS", "Tenosynovitis, NOS", "tendinous synovitis", "Tendinous synovitis", "Tenosynovitis (disorder)", "tenosynovitis (diagnosis)", "tendon sheath inflammation", "inflammation of tendon sheath", "Inflammation of tendon sheath", "Inflammation of the tendon sheath"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tenosynovitis", "shortest_name_length": 13}
{"curie": "UMLS:C1321120", "names": ["Negative pressure pulmonary edema", "Negative pressure pulmonary oedema", "Negative pressure pulmonary edema (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Negative pressure pulmonary edema", "shortest_name_length": 33}
{"curie": "UMLS:C1334285", "names": ["Ionizing Radiation-Related Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ionizing Radiation-Related Malignant Neoplasm", "shortest_name_length": 45}
{"curie": "UMLS:C5557528", "names": ["Refractory Fallopian Tube Clear Cell Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Fallopian Tube Clear Cell Adenocarcinoma", "shortest_name_length": 51}
{"curie": "MONDO:0018711", "names": ["intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome", "shortest_name_length": 81}
{"curie": "MONDO:0019199", "names": ["IGDA", "Ackerman dermatitis syndrome", "interstitial granulomatous dermatitis with arthritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "interstitial granulomatous dermatitis with arthritis", "shortest_name_length": 4}
{"curie": "UMLS:C4329382", "names": ["B-lymphoblastic leukemia lymphoma BCR-ABL1-like", "B Lymphoblastic Leukemia/Lymphoma, BCR-ABL1-Like", "B-lymphoblastic leukaemia lymphoma BCR-ABL1-like", "B-lymphoblastic leukemia lymphoma BCR-ABL1-like (morphologic abnormality)", "B Lymphoblastic Leukemia/Lymphoma with Translocations Involving Tyrosine Kinases or Cytokine Receptors"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-lymphoblastic leukemia lymphoma BCR-ABL1-like", "shortest_name_length": 47}
{"curie": "MONDO:0012076", "names": ["MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA", "Midface Hypoplasia, Obesity, Developmental Delay, and Neonatal Hypotonia", "midface hypoplasia, obesity, developmental delay, and neonatal hypotonia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "midface hypoplasia, obesity, developmental delay, and neonatal hypotonia", "shortest_name_length": 72}
{"curie": "UMLS:C0520677", "names": ["Delusional disorder, mixed", "Mixed Type Delusional Disorder", "Delusional disorder, mixed type", "delusional disorder, mixed type", "Delusional disorder, mixed type (disorder)", "delusional disorder, mixed type (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Delusional disorder, mixed type", "shortest_name_length": 26}
{"curie": "MONDO:0015812", "names": ["primary cutaneous gamma/delta-positive T-cell lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary cutaneous gamma/delta-positive T-cell lymphoma", "shortest_name_length": 54}
{"curie": "MONDO:0013357", "names": ["MMFD", "Del(17)(q11)", "Monosomy 17q11", "monosomy 17q11", "Van Asperen syndrome", "VAN ASPEREN SYNDROME", "17q11 deletion syndrome", "NF1 MICRODELETION SYNDROME", "NF1 Microdeletion Syndrome", "NF1 microdeletion syndrome", "17q11 microdeletion syndrome", "NF1 microduplication syndrome", "RNF135-related overgrowth syndrome", "17q11 deletion syndrome (disorder)", "chromosome 17q11.2 deletion syndrome", "Chromosome 17q11.2 deletion syndrome", "neurofibromatosis 1 microdeletion syndrome", "NEUROFIBROMATOSIS 1 MICRODELETION SYNDROME", "chromosome 17q11.2 deletion syndrome, 1.4Mb", "CHROMOSOME 17q11.2 DELETION SYNDROME, 1.4-MB", "chromosome 17q11.2 deletion syndrome, 1.4-MB", "neurofibromatosis type 1 microdeletion syndrome", "Neurofibromatosis type 1 microdeletion syndrome", "Overgrowth-macrocephaly-facial dysmorphism syndrome", "overgrowth-macrocephaly-facial dysmorphism syndrome", "Ring finger protein 135 related overgrowth syndrome", "Overgrowth, macrocephaly, facial dysmorphism syndrome", "macrocephaly, macrosomia, and facial dysmorphism syndrome", "RNF135 (ring finger protein 135) related overgrowth syndrome", "Overgrowth, macrocephaly, facial dysmorphism syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 17q11.2 deletion syndrome, 1.4Mb", "shortest_name_length": 4}
{"curie": "MONDO:0024535", "names": ["SGMRT1", "Singleton-Merten syndrome 1", "singleton-Merten syndrome 1", "SINGLETON-MERTEN SYNDROME 1", "IFIH1 singleton-Merten dysplasia", "singleton-Merten dysplasia caused by mutation in IFIH1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Singleton-Merten syndrome 1", "shortest_name_length": 6}
{"curie": "MONDO:0021049", "names": ["tumor vulva", "Vulva Tumor", "vulva tumor", "Vulvar Tumor", "vulvar tumor", "vulva; tumor", "tumors vulva", "tumours vulva", "tumor of vulva", "Tumor of vulva", "vulva neoplasm", "Vulva Neoplasm", "Tumor of Vulva", "neoplasm vulva", "vulval neoplasm", "vulvar neoplasm", "Vulvar neoplasm", "Tumour of vulva", "Vulval neoplasm", "Neoplasm, Vulva", "Vulva Neoplasms", "Vulvar Neoplasm", "Neoplasms, Vulva", "Vulvar Neoplasms", "Neoplasm, Vulvar", "Neoplasm of Vulva", "neoplasm of vulva", "Neoplasms, Vulvar", "Neoplasm of vulva", "Tumor of the Vulva", "Tumor of the vulva", "tumor of the vulva", "Tumour of the vulva", "Vulval neoplasm NOS", "mammalian vulva tumor", "neoplasm of the vulva", "Neoplasm of the vulva", "Neoplasm of the Vulva", "tumor of mammalian vulva", "mammalian vulva neoplasm", "neoplasm of mammalian vulva", "Neoplasm of vulva (disorder)", "neoplasm of vulva (diagnosis)", "mammalian vulva neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar neoplasm", "shortest_name_length": 11}
{"curie": "MONDO:0002957", "names": ["sarcomatoid basal cell carcinoma", "skin sarcomatoid basal cell carcinoma", "Skin Sarcomatoid Basal Cell Carcinoma", "Skin Basal Cell Carcinoma with Sarcomatoid Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sarcomatoid basal cell carcinoma", "shortest_name_length": 32}
{"curie": "UMLS:C1511259", "names": ["Borderline Ovarian Clear Cell Adenofibroma with Intraepithelial Carcinoma", "Borderline Ovarian Clear Cell Tumor/Atypical Proliferative Ovarian Clear Cell Tumor with Intraepithelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Ovarian Clear Cell Tumor/Atypical Proliferative Ovarian Clear Cell Tumor with Intraepithelial Carcinoma", "shortest_name_length": 73}
{"curie": "UMLS:C5239291", "names": ["Cutaneous Erdheim-Chester Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cutaneous Erdheim-Chester Disease", "shortest_name_length": 33}
{"curie": "UMLS:C4682638", "names": ["Stage IIA Primary Peritoneal Cancer", "Stage IIA Primary Peritoneal Cancer AJCC v8", "Stage IIA Primary Peritoneal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Primary Peritoneal Cancer AJCC v8", "shortest_name_length": 35}
{"curie": "UMLS:C0342635", "names": ["hungry bone syndrome", "Hungry bone syndrome", "Hungry bones syndrome", "'hungry bone' syndrome", "Hungry bone syndrome (disorder)", "'hungry bone' syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hungry bone syndrome", "shortest_name_length": 20}
{"curie": "MONDO:0030861", "names": ["OI21", "osteogenesis imperfecta 21", "osteogenesis imperfecta type 21", "osteogenesis imperfecta type XXI", "osteogenesis imperfecta, type 21", "osteogenesis imperfecta, TYPE XXI", "OSTEOGENESIS IMPERFECTA, TYPE XXI"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteogenesis imperfecta, type 21", "shortest_name_length": 4}
{"curie": "MONDO:0007500", "names": ["cup Ear", "Ear anomaly", "ear; anomaly", "anomaly; ear", "Ear anomalies", "ear malformation", "EAR BIRTH DEFECT", "EAR MALFORMATION", "Ear malformation", "ear malformations", "birth defects ear", "Ear abnormalities", "malformation of ear", "Malformation of ear", "Ear malformation NOS", "congenital anomaly ear", "Congenital anomaly;ear", "Abnormality of the ear", "congenital ear anomaly", "Malformation of ear, NOS", "Congenital anomaly of ear", "deformity; ear, congenital", "Unspecified anomaly of ear", "ear; deformity, congenital", "congenital ear malformation", "Congenital deformity of ear", "congenital deformity of ear", "Congenital anomalies of ear", "congenital anomaly of the ear", "Congenital anomaly of ear NOS", "Congenital abnormality of ear", "Congenital malformation of ear", "Congenital anomaly of ear, NOS", "CONGENITAL ANOMALIES OF THE EAR", "Congenital ear malformation NOS", "Congenital deformity of ear, NOS", "Unspecified congenital anomaly of ear", "Congenital ear anomaly NOS (disorder)", "congenital deformity of ear (diagnosis)", "Congenital malformation of ear (disorder)", "Congenital malformation of ear, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ear malformation", "shortest_name_length": 7}
{"curie": "UMLS:C0038663", "names": ["SUICIDE ATTEMPT", "Suicide attempt", "attempt suicide", "suicide attempt", "Suicide/attempt", "Suicide Attempt", "Attempt, Suicide", "Suicide attempts", "suicide attempts", "Attempted suicide", "attempted suicide", "attempts suicides", "Attempted Suicide", "Suicide, Attempted", "Suicide attempt(s)", "Suicide (attempted)", "Suicide (Attempted)", "Suicide attempt, NOS", "Attempted suicide NOS", "Suicide attempt (event)", "suicide attempt (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Suicide attempt", "shortest_name_length": 15}
{"curie": "UMLS:C0750818", "names": ["cns lymphomatoid granulomatosis", "Central Nervous System Lymphomatoid Granulomatosis", "central nervous system lymphomatoid granulomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Lymphomatoid Granulomatosis", "shortest_name_length": 31}
{"curie": "MONDO:0017102", "names": ["FCD type IIb", "isolated focal cortical dysplasia type IIb"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated focal cortical dysplasia type IIb", "shortest_name_length": 12}
{"curie": "MONDO:0018872", "names": ["M7", "AMKL", "AMegL", "AML M7", "Fab M7", "FAB M7", "Thrombocytic leukemia", "thrombocytic leukaemia", "Thrombocytic leukaemia", "leukemia; thrombocytic", "thrombocytic; leukemia", "Megakaryocytic Leukemia", "megakaryocytic myelosis", "Megakaryocytic leukemia", "megakaryocytic leukemia", "Megakaryocytic myelosis", "leukemia megakaryocytic", "megakaryocytic; myelosis", "Megakaryocytic Leukemias", "leukemia; megakaryocytic", "megakaryocytic; leukemia", "LEUKEMIA, MEGAKARYOCYTIC", "Megakaryocytic leukaemia", "Leukemia, Megakaryocytic", "[M]Thrombocytic leukemia", "Megakaryocytoid leukemia", "myelosis; megakaryocytic", "Acute M7 Myeloid Leukemia", "Megakaryoblastic leukemia", "[M]Thrombocytic leukaemia", "Acute myeloid leukemia M7", "acute M7 myeloid leukemia", "Leukemias, Megakaryocytic", "megakaryoblastic leukemia", "acute myeloid leukemia M7", "[M]Megakaryocytic leukemia", "Malignant megakaryocytosis", "Megakaryoblastic leukaemia", "Myeloid Leukemia, Acute, M7", "[M]Megakaryocytic leukaemia", "Megakaryocytic leukemia NOS", "Leukemia, Myeloid, Acute, M7", "Megakaryocytic leukaemia NOS", "acute megakaryocytic leukemia", "Acute megakaryocytic leukemia", "Acute Megakaryocytic Leukemia", "Acute megakaryocytic leukaemia", "Leukemia, Acute Megakaryocytic", "Megakaryocytic Leukemia, Acute", "acute megakaryocytic leukemias", "Acute Megakaryocytic Leukemias", "leukemia acute megakaryoblastic", "acute megakaryoblastic leukemia", "Leukemia, Megakaryocytic, Acute", "Megakaryocytic Leukemias, Acute", "Acute megakaryoblastic leukemia", "Acute Megakaryoblastic Leukemia", "Leukemias, Acute Megakaryocytic", "Acute Megakaryoblastic Leukemias", "Megakaryoblastic Leukemia, Acute", "Leukemia, Acute Megakaryoblastic", "Acute megakaryoblastic leukaemia", "acute megakaryoblastic leukaemia", "Leukemias, Acute Megakaryoblastic", "Megakaryoblastic Leukemias, Acute", "Leukemia, Megakaryoblastic, Acute", "acute myeloblastic leukemia type 7", "Megakaryocytic leukemia (disorder)", "leukemia, megakaryocytic, malignant", "Acute megakaryoblastic leukemia NOS", "megakaryocytic leukemia (diagnosis)", "LEUKEMIA, MEGAKARYOCYTIC, MALIGNANT", "M7 - Acute megakaryoblastic leukemia", "M7 OR Acute Megakaryoblastic Leukemia", "M7 - Acute megakaryoblastic leukaemia", "acute megakaryoblastic leukemia, FAB M7", "Acute megakaryoblastic leukemia, FAB M7", "acute megakaryoblastic leukaemia, FAB M7", "Acute megakaryoblastic leukaemia, FAB M7", "Acute megakaryoblastic leukemia (disorder)", "Acute megakaryoblastic leukemia, morphology", "acute megakaryoblastic leukemia (diagnosis)", "Acute megakaryoblastic leukaemia, morphology", "acute megakaryoblastic leukemia (FAB type M7)", "Acute Megakaryoblastic Leukemia (Fab Type M7)", "Acute Megakaryoblastic Leukemia (FAB Type M7)", "Acute megakaryoblastic leukemia, morphology (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute megakaryoblastic leukemia", "shortest_name_length": 2}
{"curie": "UMLS:C1518189", "names": ["Malignant Lymphoma, Large Cell Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Lymphoma, Large Cell Type", "shortest_name_length": 35}
{"curie": "MONDO:0008224", "names": ["HYPP", "HyperPP", "hyperPP", "hyperKPP", "HyperKPP", "Primary hyperPP", "Hyperkalemic PP", "primary hyperPP", "hyperkalemic PP", "Familial hyperPP", "familial hyperPP", "Gamstorp Disease", "GAMSTORP DISEASE", "Gamstorp disease", "Disease, Gamstorp", "Hereditary adynamia", "periodic paralysis ii", "Periodic paralysis II", "Gamstorp Episodic Adynamy", "Gamstorp episodic adynamy", "Myotonic periodic paralysis", "Myotonic Periodic Paralysis", "Sodium Channel Muscle Disease", "sodium channel muscle disease", "Adynamia Episodica Hereditaria", "ADYNAMIA EPISODICA HEREDITARIA", "adynamia episodica hereditaria", "Adynamia episodica hereditaria", "Periodic hyperkalemic paralysis", "hyperkalemic paralysis periodic", "HYPERKALEMIC PERIODIC PARALYSIS", "Hyperkalemic periodic paralysis", "hyperkalemic periodic paralysis", "Hyperkalemic Periodic Paralysis", "periodic paralysis hyperkalemic", "Hyperkalaemic periodic paralysis", "hyperkalaemic periodic paralysis", "Paralysis, Hyperkalemic Periodic", "PERIODIC PARALYSIS, HYPERKALEMIC", "hyperkalemic periodic paralysis, type 2", "Primary hyperkalemic periodic paralysis", "primary hyperkalemic periodic paralysis", "Primary Hyperkalemic Periodic Paralysis", "Familial hyperkalemic periodic paralysis", "Familial Hyperkalemic Periodic Paralysis", "hyperkalemic periodic paralysis syndrome", "familial hyperkalemic periodic paralysis", "Familial hyperkalaemic periodic paralysis", "Hyperkalemic Periodic Paralysis, Familial", "Hyperkalemic periodic paralysis (familial)", "Paralysis, Periodic, Hyperkalemic, Familial", "Familial hyperkalemic periodic paralysis (disorder)", "NORMOKALEMIC PERIODIC PARALYSIS, POTASSIUM-SENSITIVE", "hyperkalemic periodic paralysis syndrome (diagnosis)", "Normokalemic Periodic Paralysis, Potassium-Sensitive", "normokalemic periodic paralysis, potassium-sensitive", "adynamia episodica hereditaria with or without myotonia", "ADYNAMIA EPISODICA HEREDITARIA WITH OR WITHOUT MYOTONIA", "Adynamia Episodica Hereditaria with or without Myotonia", "familial hyperkalemic periodic paralysis (disorder) [ambiguous]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperkalemic periodic paralysis", "shortest_name_length": 4}
{"curie": "UMLS:C4331407", "names": ["Thoracic Spinal Cord Ependymal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thoracic Spinal Cord Ependymal Tumor", "shortest_name_length": 36}
{"curie": "MONDO:0009133", "names": ["UTS", "DES", "CAMRQ", "VLDLRCH", "Disequilibrium", "Dysequilibrium", "CAMRQ syndrome", "Halpern syndrome", "Uner Tan syndrome", "POSTDIALYSIS SYNDROME", "dysequilibrium syndrome", "Dysequilibrium syndrome", "Disequilibrium Syndrome", "Dialysis disequilibrium", "disequilibrium syndrome", "Disequilibrium syndrome", "VLDLR Cerebellar Hypoplasia", "DES - Dysequilibrium syndrome", "dysequilibrium syndrome (DES)", "disturbed equilibrium syndrome", "dialysis dysequilibrium syndrome", "Dialysis disequilibrium syndrome", "DIALYSIS DISEQUILIBRIUM SYNDROME", "Dialysis Disequilibrium Syndrome", "Dysequilibrium syndrome (disorder)", "HEMODIALYSIS DISEQUILIBRIUM SYNDROME", "cerebellar hypoplasia, VLDLR associated", "Dialysis disequilibrium syndrome (disorder)", "sensimotor induction in disturbed equilibrium syndrome", "cerebellar ataxia, mental retardation, and dysequilibrium", "nonprogressive cerebellar disorder with mental retardation", "cerebellar disorder, nonprogressive, with mental retardation", "cerebellar ataxia, intellectual disability, and dysequilibrium", "cerebellar ataxia, mental retardation and dysequlibrium syndrome", "non-progressive cerebellar ataxia-intellectual disability syndrome", "Non-progressive cerebellar ataxia-intellectual disability syndrome", "cerebellar ataxia-intellectual disability-dysequilibrium syndrome syndrome", "Cerebellar ataxia-intellectual disability-dysequilibrium syndrome syndrome", "Cerebellar Ataxia, Mental Retardation, and Dysequilibrium Syndrome 1 (CAMRQ1)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellar ataxia, intellectual disability, and dysequilibrium", "shortest_name_length": 3}
{"curie": "MONDO:0031376", "names": ["congenital disorder of deglycosylation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital disorder of deglycosylation", "shortest_name_length": 38}
{"curie": "MONDO:0007739", "names": ["HD", "Huntington", "Huntington chorea", "huntington chorea", "Huntington Chorea", "HUNTINGTON CHOREA", "Chorea, Huntington", "huntingtons chorea", "Huntington Disease", "Huntingtons Chorea", "Huntington; chorea", "Chorea;Huntingtons", "Huntington disease", "Huntingtons chorea", "HUNTINGTON DISEASE", "chorea; Huntington", "Huntingtons Disease", "huntingtons disease", "Huntington's chorea", "huntington's chorea", "Huntington's Chorea", "Huntington's disease", "Huntington's Disease", "huntington's disease", "Chorea, Huntington's", "HD - Huntington chorea", "HC - Huntington chorea", "Chronic progressive chorea", "Huntington's chorea (disorder)", "Huntington's chorea (diagnosis)", "Chronic progressive hereditary chorea", "CHOREA, CHRONIC PROGRESSIVE HEREDITARY", "Huntington Chronic Progressive Hereditary Chorea", "Chronic Progressive Hereditary Chorea (Huntington)", "Chorea, Chronic Progressive Hereditary (Huntington)", "Progressive Chorea, Chronic Hereditary (Huntington)", "Progressive Chorea, Hereditary, Chronic (Huntington)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Huntington disease", "shortest_name_length": 2}
{"curie": "MONDO:0043166", "names": ["Pancreatic lipomatosis duodenal stenosis", "pancreatic lipomatosis duodenal stenosis", "Pancreatic lipomatosis and duodenal atresia", "pancreatic lipomatosis and duodenal atresia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic lipomatosis duodenal stenosis", "shortest_name_length": 40}
{"curie": "MONDO:0044956", "names": ["Accessory Sinus Mucoepidermoid Carcinoma", "accessory sinus mucoepidermoid carcinoma", "paranasal sinus mucoepidermoid carcinoma", "Paranasal Sinus Mucoepidermoid Carcinoma", "mucoepidermoid carcinoma of accessory sinus", "mucoepidermoid carcinoma of paranasal sinus", "Mucoepidermoid Carcinoma of Accessory Sinus", "Mucoepidermoid Carcinoma of Paranasal Sinus", "Mucoepidermoid Carcinoma of the Paranasal Sinus", "mucoepidermoid carcinoma of the paranasal sinus", "mucoepidermoid carcinoma of the accessory sinus", "Mucoepidermoid Carcinoma of the Accessory Sinus", "mucoepidermoid carcinoma of accessory sinus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paranasal sinus mucoepidermoid carcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0024886", "names": ["Serous adenofibroma", "Serous Adenofibroma", "serous adenofibroma", "Serous cystadenofibroma", "serous; adenofibroma, unspecified site", "adenofibroma; serous, unspecified site", "Serous adenofibroma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "serous adenofibroma", "shortest_name_length": 19}
{"curie": "MONDO:0015664", "names": ["idiopathic pulmonary artery dilatation", "idiopathic dilatation of the pulmonary artery"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic pulmonary artery dilatation", "shortest_name_length": 38}
{"curie": "MONDO:0015261", "names": ["pseudopelade", "Pseudopelade", "alopecia scar", "alopecia; scar", "scarring alopecia", "Scarring alopecia", "Alopecia scarring", "ALOPECIA SCARRING", "Brocq pseudopelade", "Alopecia, scarring", "Alopecia cicatrisata", "alopecia cicatrisata", "ALOPECIA CICATRISATA", "Alopecia Cicatrisata", "Cicatricial alopecia", "cicatricial alopecia", "Alopecia Cicatrisatas", "Pseudopelade of Brocq", "cicatricial; alopecia", "pseudopelade of Brocq", "alopecia; cicatricial", "pseudo pelade of Brocq", "pseudo-pelade of Brocq", "Pseudopelade (disorder)", "pseudopelade (diagnosis)", "Scarring alopecia (disorder)", "Cicatricial alopecia, unspecified", "Cicatricial alopecia [scarring hair loss]", "cicatricial alopecia [scarring hair loss]", "cicatricial alopecia [scarring hair loss] (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudopelade of Brocq", "shortest_name_length": 12}
{"curie": "MONDO:0018144", "names": ["congenital myasthenic syndromes with glycosylation defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myasthenic syndromes with glycosylation defect", "shortest_name_length": 57}
{"curie": "MONDO:0001732", "names": ["Trigonitis", "TRIGONITIS", "trigonitis", "Trigonitis, NOS", "Trigonitis (disorder)", "trigonitis (diagnosis)", "trigone of urinary bladder inflammation", "inflammation of trigone of urinary bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trigonitis", "shortest_name_length": 10}
{"curie": "UMLS:C5556514", "names": ["Metastatic Hydatidiform Mole"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Hydatidiform Mole", "shortest_name_length": 28}
{"curie": "UMLS:C0855187", "names": ["Stage 0 Bladder Squamous Cell Cancer", "Bladder squamous cell carcinoma stage 0", "Stage 0 Bladder Squamous Cell Carcinoma", "Squamous cell bladder carcinoma stage 0", "Stage 0 Squamous Cell Carcinoma of Bladder", "Stage 0 Squamous Cell Carcinoma of the Bladder", "Squamous cell carcinoma of the bladder stage 0", "Stage 0 Bladder Squamous Cell Carcinoma AJCC v7", "Stage 0 Bladder Squamous Cell Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder squamous cell carcinoma stage 0", "shortest_name_length": 36}
{"curie": "MONDO:0013391", "names": ["LKDMN", "SCP2 deficiency", "sterol carrier protein 2 deficiency", "STEROL CARRIER PROTEIN 2 DEFICIENCY", "leukoencephalopathy - dystonia - motor neuropathy", "LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY", "leukoencephalopathy with dystonia and motor neuropathy", "leukoencephalopathy-dystonia-motor neuropathy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sterol carrier protein 2 deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C1708775", "names": ["Lung Monophasic Synovial Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Monophasic Synovial Sarcoma", "shortest_name_length": 32}
{"curie": "MONDO:0005870", "names": ["Necatorosis", "Necatoriases", "Necatoriasis", "necatoriasis", "NECATORIASIS", "Necatoriasis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "necatoriasis", "shortest_name_length": 11}
{"curie": "MONDO:0030480", "names": ["DFNB119", "deafness, autosomal recessive 119", "DEAFNESS, AUTOSOMAL RECESSIVE 119", "hearing loss, autosomal recessive 119"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hearing loss, autosomal recessive 119", "shortest_name_length": 7}
{"curie": "MONDO:0012709", "names": ["MCOPCB5", "microphthalmia with coloboma 5", "MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 5", "Microphthalmia, Isolated, with Coloboma 5", "microphthalmia, isolated, with coloboma 5", "SHH microphthalmia, isolated, with coloboma", "Shh microphthalmia, isolated, with coloboma", "microphthalmia, isolated, with coloboma type 5", "MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 5 (disorder)", "microphthalmia, isolated, with coloboma caused by mutation in SHH", "microphthalmia, isolated, with coloboma caused by mutation in Shh"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microphthalmia, isolated, with coloboma 5", "shortest_name_length": 7}
{"curie": "UMLS:C1336550", "names": ["T-Cell Proliferation of Uncertain Malignant Potential"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-Cell Proliferation of Uncertain Malignant Potential", "shortest_name_length": 53}
{"curie": "MONDO:0036918", "names": ["punctate acrokeratoderma freckle-like pigmentation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "punctate acrokeratoderma freckle-like pigmentation", "shortest_name_length": 50}
{"curie": "MONDO:0000062", "names": ["isolated microphthalmia", "microphthalmia, isolated", "nonsyndromic microphthalmia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated microphthalmia", "shortest_name_length": 23}
{"curie": "UMLS:C0154043", "names": ["Benign Pineal Area Tumor", "Benign Pineal Region Tumor", "Benign Pineal Area Neoplasm", "benign tumor of pineal body", "Benign tumor of pineal gland", "Benign tumour of pineal gland", "Benign Pineal Region Neoplasm", "benign neoplasm of pineal body", "Benign neoplasm of pineal body", "Benign Pineal Parenchymal Tumor", "Benign neoplasm of pineal gland", "Benign Tumor of Pineal Parenchyma", "Benign Pineal Parenchymal Neoplasm", "Benign neoplasm of pineal gland NOS", "Benign Neoplasm of Pineal Parenchyma", "Pineal Parenchymal Neoplasms, Benign", "Benign Tumor of the Pineal Parenchyma", "Benign Neoplasm of the Pineal Parenchyma", "Benign neoplasm of pineal gland (disorder)", "benign neoplasm of pineal body (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign neoplasm of pineal gland", "shortest_name_length": 24}
{"curie": "MONDO:0033563", "names": ["RP90", "retinitis pigmentosa 90", "RETINITIS PIGMENTOSA 90"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 90", "shortest_name_length": 4}
{"curie": "UMLS:C0855003", "names": ["Lung carcinoma stage I", "Carcinoma of lung stage I", "Pulmonary carcinoma stage I", "Lung carcinoma cell type unspecified stage I", "Carcinoma of lung cell type unspecified stage I", "Pulmonary carcinoma cell type unspecified stage I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung carcinoma cell type unspecified stage I", "shortest_name_length": 22}
{"curie": "UMLS:C0456126", "names": ["Neonatal rickets", "Neonatal Rickets", "Rickets of prematurity", "Rickets of Prematurity", "Osteopenia of Prematurity", "Neonatal rickets (disorder)", "Metabolic Bone Disease of Prematurity", "Metabolic bone disease of prematurity", "Metabolic bone disease of prematurity (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neonatal rickets", "shortest_name_length": 16}
{"curie": "UMLS:C5244027", "names": ["COVID-19 pneumonia", "SARS-CoV-2 pneumonia", "COVID-19 pneumonitis", "Pneumonia caused by 2019-nCoV", "Pneumonia caused by SARS-CoV-2", "Novel COVID-19-infected pneumonia", "Pneumonia caused by 2019 novel coronavirus", "Pneumonia caused by severe acute respiratory syndrome coronavirus 2", "Pneumonia caused by severe acute respiratory syndrome coronavirus 2 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pneumonia caused by SARS-CoV-2", "shortest_name_length": 18}
{"curie": "UMLS:C5568423", "names": ["BA/CMPT", "Lung Peripheral Papilloma", "Lung Solitary Peripheral Ciliated Glandular Papilloma", "Bronchiolar adenoma/ciliated muconodular papillary tumor", "Bronchiolar Adenoma/Ciliated Muconodular Papillary Tumor", "Bronchiolar adenoma/ciliated muconodular papillary tumour", "BA/CMPT - bronchiolar adenoma/ciliated muconodular papillary tumor", "BA/CMPT - bronchiolar adenoma/ciliated muconodular papillary tumour", "Bronchiolar adenoma/ciliated muconodular papillary tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bronchiolar adenoma/ciliated muconodular papillary tumor", "shortest_name_length": 7}
{"curie": "MONDO:0018267", "names": ["combined cervical dystonia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined cervical dystonia", "shortest_name_length": 26}
{"curie": "MONDO:0016256", "names": ["Hennekam syndrome", "Hennekam lymphangiectasia-lymphedema syndrome", "Hennekam Lymphangiectasia-Lymphedema Syndrome", "Hennekam lymphangiectasia lymphedema syndrome", "HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME", "Lymphangiectasies and lymphedema Hennekam type", "Hennekam lymphangiectasia-lymphoedema syndrome", "lymphangiectasies and lymphedema Hennekam type", "Hennekam lymphangiectasia-lymphedema syndrome (disorder)", "Hennekam lymphangiectasia-lymphedema syndrome (diagnosis)", "lymphedem-lymphangiectasia-intellectual disability syndrome", "Lymphedema-lymphangiectasia-intellectual disability syndrome", "lymphedema-lymphangiectasia-intellectual disability syndrome", "Lymphedema, lymphangiectasia, intellectual disability syndrome", "Lymphoedema, lymphangiectasia, intellectual disability syndrome", "intestinal lymphagiectasia-lymphedema-mental retardation syndrome", "intestinal lymphagiectasia lymphedema intellectual deficit syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hennekam syndrome", "shortest_name_length": 17}
{"curie": "UMLS:C5421212", "names": ["Locally Advanced Lung Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Lung Adenocarcinoma", "shortest_name_length": 36}
{"curie": "MONDO:0016725", "names": ["pineal parenchymal tumor of intermediate differenciation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pineal parenchymal tumor of intermediate differenciation", "shortest_name_length": 56}
{"curie": "MONDO:0019486", "names": ["myoclonic epilepsy of infancy", "benign myoclonus epilepsy of infancy", "benign myoclonic epilepsy of infancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myoclonic epilepsy of infancy", "shortest_name_length": 29}
{"curie": "MONDO:0012367", "names": ["RP31", "RP 31", "retinitis pigmentosa 31", "RETINITIS PIGMENTOSA 31", "Retinitis Pigmentosa 31", "TOPORS retinitis pigmentosa", "retinitis pigmentosa type 31", "retinitis pigmentosa caused by mutation in TOPORS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 31", "shortest_name_length": 4}
{"curie": "UMLS:C0267176", "names": ["DIABETIC GASTROPARESIS", "Diabetic gastroparesis", "diabetic gastroparesis", "Gastroparesis with diabetes mellitus", "Gastroparesis due to diabetes mellitus", "Gastroparesis due to diabetes mellitus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastroparesis due to diabetes mellitus", "shortest_name_length": 22}
{"curie": "MONDO:0040674", "names": ["orgasm disorder", "Abnormal orgasm", "Abnormal Orgasm", "Orgasm abnormal", "Orgasm disorder", "abnormal orgasm", "disorder; orgasm", "orgasm disorders", "disorders orgasm", "orgasm; disorder", "orgasmic disorder", "Orgasmic Disorder", "Orgasmic disorder", "Orgasmic Disorders", "Disorders, Orgasmic", "dysfunction; orgasm", "Abnormal orgasm, NOS", "Orgasm disorder, NOS", "Orgasmic dysfunction", "orgasmic dysfunction", "Orgasm disorder (disorder)", "orgasmic disorder (diagnosis)", "dysfunction; sexual, orgasmic dysfunction (male) (female)", "sexual; dysfunction, orgasmic dysfunction (male) (female)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orgasm disorder", "shortest_name_length": 15}
{"curie": "UMLS:C4763823", "names": ["Kidney Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kidney Neuroendocrine Neoplasm", "shortest_name_length": 30}
{"curie": "MONDO:0700038", "names": ["TDP-43 proteinopathy", "TDP-43 Proteinopathy", "Proteinopathy, TDP-43", "TDP 43 Proteinopathies", "TDP-43 Proteinopathies", "Proteinopathies, TDP-43"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "TDP-43 proteinopathy", "shortest_name_length": 20}
{"curie": "MONDO:0031332", "names": ["GT", "GT1", "BDPLT2", "Thrombasthenia", "thrombasthenia", "THROMBASTHENIA", "THROMBOASTHENIA", "thromboasthenia", "Thromboasthenia", "Thrombasthenias", "Atypical Platelet", "Abnormal platelet", "abnormal platelet", "GLANZMANN DISEASE", "Abnormal;platelet", "Abnormal Platelet", "Platelets abnormal", "ABNORMAL PLATELETS", "Abnormal platelets", "Thrombocytasthenia", "abnormal platelets", "thrombocytasthenia", "PLATELETS ABNORMAL", "Glanzmann's disease", "Thrombasthenia, NOS", "glanzmann's disease", "Glanzsmann's disease", "PLATELET ABNORMALITY", "Thromboasthenia, NOS", "Glanzmann's syndrome", "platelet abnormality", "PLATELET ABNORMALITIES", "Platelet abnormalities", "Blood platelet disease", "abnormalities platelet", "platelet abnormalities", "abnormalities platelets", "Thrombosthenin disorder", "GLANZMANN THROMBASTHENIA", "Glanzmann thrombasthenia", "Glanzmann Thrombasthenia", "glanzmann thrombasthenia", "Hereditary thrombasthenia", "glanzmanns thrombasthenia", "Thrombasthenia, Glanzmann", "Glanzmann thromboasthenia", "hereditary thrombasthenia", "thrombasthenia (diagnosis)", "glanzmann's thrombasthenia", "Glanzmann thrombasthenia 1", "Glanzmann-Naegeli disorder", "Thrombasthenia, hereditary", "Platelet abnormalities NOS", "GLANZMANN THROMBASTHENIA 1", "Hereditary thromboasthenia", "Glanzmann's thrombasthenia", "Thrombasthenia, hemorrhagic", "THROMBOCYTES ABNORMAL (NOS)", "Thrombocytes abnormal (NOS)", "Abnormality of thrombocytes", "Diacyclothrombopathia 2B 3A", "Glycoprotein IIb/IIIa defect", "glycoprotein IIb/IIIa defect", "GP IIb-IIIa COMPLEX DEFICIENCY", "thrombocytasthenia (diagnosis)", "Deficiency of GP 2b 3a Complex", "deficiency of GP 2B 3A complex", "Hereditary thromboasthenia, NOS", "Glanzmann thrombasthenia type A", "Glanzmann Thrombasthenia, Type A", "deficiency of GP IIb-IIIa complex", "platelet-type bleeding disorder 2", "GP IIb-IIIa Complex, deficiency of", "GP IIb IIIa Complex, Deficiency Of", "GP IIb-IIIa Complex, Deficiency Of", "bleeding disorder, Platelet-type, 2", "BLEEDING DISORDER, PLATELET-TYPE, 2", "Glanzmann's thrombosthenin disorder", "hereditary thrombasthenia (diagnosis)", "Glanzmann's thrombasthenia (disorder)", "Hereditary hemorrhagic thrombasthenia", "Platelet Glycoprotein 2b-3a Deficiency", "Platelet Glycoprotein 2b 3a Deficiency", "Hereditary haemorrhagic thrombasthenia", "Platelet glycoprotein 2B 3A deficiency", "PLATELET FIBRINOGEN RECEPTOR DEFICIENCY", "thrombasthenia of Glanzmann and Naegeli", "Thrombasthenia of Glanzmann and Naegeli", "THROMBASTHENIA OF GLANZMANN AND NAEGELI", "GLYCOPROTEIN COMPLEX IIb-IIIa DEFICIENCY", "Platelet glycoprotein IIb-IIIa deficiency", "Platelet Glycoprotein IIb-IIIa Deficiency", "PLATELET GLYCOPROTEIN IIb-IIIa DEFICIENCY", "Platelet Glycoprotein IIb IIIa Deficiency", "platelet glycoprotein IIb-IIIa deficiency", "deficiency of platelet fibrinogen receptor", "Platelet Fibrinogen Receptor, Deficiency of", "Abnormal platelet (morphologic abnormality)", "Platelet fibrinogen receptor, deficiency of", "deficiency of glycoprotein complex IIb-IIIa", "Glycoprotein Complex IIb IIIa, Deficiency Of", "Glycoprotein Complex IIb-IIIa, Deficiency Of", "glycoprotein Complex IIb-IIIa, deficiency of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Glanzmann thrombasthenia 1", "shortest_name_length": 2}
{"curie": "MONDO:0009909", "names": ["progesterone resistance", "PROGESTERONE RESISTANCE", "Progesterone Resistance", "Pseudocorpus Luteum Insufficiency", "PSEUDOCORPUS LUTEUM INSUFFICIENCY", "pseudocorpus luteum insufficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progesterone resistance", "shortest_name_length": 23}
{"curie": "UMLS:C3698122", "names": ["Atypical Ewing Sarcoma", "Large Cell Ewing Tumor", "Large Cell Ewing Sarcoma", "Atypical Ewing's sarcoma", "Large cell Ewing sarcoma of bone", "Large cell Ewing's sarcoma of bone", "Large cell Ewing sarcoma of bone (disorder)", "Large cell Ewing's sarcoma of bone (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Large cell Ewing sarcoma of bone", "shortest_name_length": 22}
{"curie": "UMLS:C0575269", "names": ["Thoracic Spine Kyphosis", "THORACIC SPINE KYPHOSIS", "Kyphosis of dorsal spine", "Kyphosis of thoracic spine", "Kyphosis deformity of thoracic spine", "Kyphosis deformity of thoracic spine (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kyphosis of thoracic spine", "shortest_name_length": 23}
{"curie": "UMLS:C1328327", "names": ["Gastroesophageal sphincter insufficiency", "Gastrooesophageal sphincter insufficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrooesophageal sphincter insufficiency", "shortest_name_length": 40}
{"curie": "MONDO:0015003", "names": ["DYT29", "DYTOABG", "Dystonia 29", "MEPAN SYNDROME", "MEPAN syndrome", "DYT29 - dystonia 29", "dystonia 29, childhood-onset", "DYSTONIA 29, CHILDHOOD-ONSET", "Autosomal recessive childhood-onset dystonia DYT29 type", "Autosomal recessive childhood-onset dystonia, DYT29 type", "Childhood-onset generalized dystonia-optic atrophy syndrome", "Childhood-onset generalised dystonia, optic atrophy syndrome", "Childhood-onset generalized dystonia, optic atrophy syndrome", "dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities", "DYSTONIA, CHILDHOOD-ONSET, WITH OPTIC ATROPHY AND BASAL GANGLIA ABNORMALITIES", "Mitochondrial enoyl CoA reductase protein-associated neurodegeneration syndrome", "Mitochondrial enoyl coenzyme A reductase protein-associated neurodegeneration syndrome", "dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities; DYTOABG", "Mitochondrial enoyl coenzyme A reductase protein-associated neurodegeneration syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities", "shortest_name_length": 5}
{"curie": "MONDO:0018212", "names": ["familial CAD", "hereditary CAD", "familial cervical artery dissection", "hereditary cervical artery dissection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial cervical artery dissection", "shortest_name_length": 12}
{"curie": "MONDO:0009765", "names": ["ocular myopathy with curare sensitivity", "OCULAR MYOPATHY WITH CURARE SENSITIVITY", "Ocular Myopathy with Curare Sensitivity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ocular myopathy with curare sensitivity", "shortest_name_length": 39}
{"curie": "UMLS:C0403745", "names": ["uterus; perforation, IUD", "perforation; uterus, IUD", "Perforation of uterus - IUD", "Uterine perforation by intrauterine contraceptive device", "Uterine perforation by intrauterine contraceptive device (disorder)", "Perforation of uterus due to intrauterine contraceptive device (IUCD)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine perforation by intrauterine contraceptive device", "shortest_name_length": 24}
{"curie": "UMLS:C5419388", "names": ["Ear or Labyrinth Problem", "Unspecified Ear or Labyrinth Problem"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ear or Labyrinth Problem", "shortest_name_length": 24}
{"curie": "UMLS:C1854520", "names": ["Sebastian Syndrome", "Sebastian Platelet Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sebastian Syndrome", "shortest_name_length": 18}
{"curie": "UMLS:C0342245", "names": ["Diabetic oculopathy", "Diabetic Eye Disease", "eye disease diabetic", "diabetic eye disease", "Diabetic eye disease", "diabetic diseases eye", "Diabetic Eye Problems", "Diabetic oculopathy, NOS", "Diabetic eye disease NOS", "Diabetic eye disease, NOS", "Ophthalmic manifestations of diabetes", "Eye disorder due to diabetes mellitus", "diabetes with ophthalmic manifestations", "Diabetes with ophthalmic manifestations", "Disorder of eye due to diabetes mellitus", "diabetes mellitus with ophthalmic manifestations", "Disorder of eye due to diabetes mellitus (disorder)", "diabetes mellitus with ophthalmic manifestations (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disorder of eye due to diabetes mellitus", "shortest_name_length": 19}
{"curie": "MONDO:0044631", "names": ["early-onset familial noncirrhotic portal hypertension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "early-onset familial noncirrhotic portal hypertension", "shortest_name_length": 53}
{"curie": "UMLS:C1334622", "names": ["Malignant Submandibular Gland Mixed Tumor", "Malignant Mixed Tumor of Submandibular Gland", "Malignant Submandibular Gland Mixed Neoplasm", "Malignant Mixed Neoplasm of Submandibular Gland", "Malignant Mixed Tumor of the Submandibular Gland", "Malignant Mixed Neoplasm of the Submandibular Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Submandibular Gland Mixed Tumor", "shortest_name_length": 41}
{"curie": "UMLS:C3888451", "names": ["Toxic leukoencephalopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Toxic leukoencephalopathy", "shortest_name_length": 25}
{"curie": "MONDO:0006824", "names": ["krebs 2 carcinoma", "Krebs 2 carcinoma", "Krebs 2 Carcinoma", "Carcinoma, Krebs 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Krebs 2 carcinoma", "shortest_name_length": 17}
{"curie": "UMLS:C1333774", "names": ["Inflammatory Gastric Pseudotumor", "Inflammatory Pseudotumor of Stomach", "Inflammatory Pseudotumor of the Stomach", "Gastric Inflammatory Myofibroblastic Tumor", "Inflammatory Myofibroblastic Tumor of Stomach", "Gastric Inflammatory Myofibroblastic Neoplasm", "Inflammatory Myofibroblastic Neoplasm of Stomach", "Inflammatory Myofibroblastic Tumor of the Stomach", "Inflammatory Myofibroblastic Neoplasm of the Stomach"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Inflammatory Myofibroblastic Tumor", "shortest_name_length": 32}
{"curie": "MONDO:0009749", "names": ["gan", "GAN1", "neuropathy, giant axonal", "giant axonal neuropathy-1", "Giant Axonal Neuropathy 1", "giant axonal neuropathy 1", "GIANT AXONAL NEUROPATHY 1", "gan giant axonal neuropathy", "GAN giant axonal neuropathy", "giant axonal neuropathy type 1", "Giant Axonal Neuropathy 1 (GAN1)", "Neuropathy, Giant Axonal, Autosomal Recessive", "giant axonal neuropathy 1, autosomal recessive", "GIANT AXONAL NEUROPATHY 1, AUTOSOMAL RECESSIVE", "giant axonal neuropathy caused by mutation in GAN", "giant axonal neuropathy caused by mutation in gan"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "giant axonal neuropathy 1", "shortest_name_length": 3}
{"curie": "MONDO:0100012", "names": ["paratenonitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paratenonitis", "shortest_name_length": 13}
{"curie": "MONDO:0017243", "names": ["bullous DCM", "bullous diffuse cutaneous mastocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bullous diffuse cutaneous mastocytosis", "shortest_name_length": 11}
{"curie": "UMLS:C0393682", "names": ["Lateral temporal epilepsy", "Lateral Temporal Epilepsy", "Epilepsy, Lateral Temporal", "Lateral Temporal Epilepsies", "Epilepsies, Lateral Temporal", "temporal lobe epilepsy lateral", "Lateral temporal epilepsy (disorder)", "Lateral temporal epilepsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epilepsy, Lateral Temporal", "shortest_name_length": 25}
{"curie": "MONDO:0003518", "names": ["Thymic Teratoma", "mediastinum teratoma", "Mediastinal Teratoma", "Mediastinal teratoma", "teratoma of mediastinum", "Teratoma of Mediastinum", "Teratoma of the Mediastinum", "Teratoma of the mediastinum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mediastinum teratoma", "shortest_name_length": 15}
{"curie": "MONDO:0013818", "names": ["THES2", "TRICHOHEPATOENTERIC syndrome 2", "Trichohepatoenteric syndrome 2", "trichohepatoenteric syndrome 2", "TRICHOHEPATOENTERIC SYNDROME 2", "Trichohepatoenteric syndrome type 2", "SKIV2L tricho-hepato-enteric syndrome", "tricho-hepato-enteric syndrome caused by mutation in SKIV2L"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichohepatoenteric syndrome 2", "shortest_name_length": 5}
{"curie": "MONDO:0002494", "names": ["AODR disorder", "substance-related disorder", "Substance Related Disorder", "Substance-Related Disorder", "Related Disorder, Substance", "Substance-Related Disorders", "Disorder, Substance Related", "Related Disorders, Substance", "Disorders, Substance Related", "substance induced mood disorders", "Alcohol or Other Drug Related disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "substance-related disorder", "shortest_name_length": 13}
{"curie": "MONDO:0013980", "names": ["PPKP1B", "PALMOPLANTAR KERATODERMA, PUNCTATE TYPE IB", "palmoplantar keratoderma, punctate type ib", "palmoplantar keratoderma, punctate type IB", "keratoderma, palmoplantar, punctate type IB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "palmoplantar keratoderma, punctate type ib", "shortest_name_length": 6}
{"curie": "MONDO:0019951", "names": ["Rigid spine syndrome", "rigid spine syndrome", "rigid spine muscular dystrophy-1", "rigid spine congenital muscular dystrophy", "desmin-related myopathies with Mallory bodies", "muscular dystrophy, congenital, merosin positive with early spine rigidity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rigid spine syndrome", "shortest_name_length": 20}
{"curie": "UMLS:C0857153", "names": ["Nodal block", "block; nodal", "nodal; block"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nodal block", "shortest_name_length": 11}
{"curie": "MONDO:0001385", "names": ["Cortical Blindness", "Cortical blindness", "Blindness cortical", "BLINDNESS CORTICAL", "blindness cortical", "cortical blindness", "CORTICAL BLINDNESS", "Blindness, Cortical", "Cortical blindness (disorder)", "cortical blindness (diagnosis)", "cortical blindness was observed", "cortical blindness (physical finding)", "disorders of visual cortex cortical blindness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cortical blindness", "shortest_name_length": 18}
{"curie": "MONDO:0013577", "names": ["LIPEDEMA", "lipedema", "Lipedema", "Lipoedema", "lipoedema", "Lipedemas", "Lipoedemas", "Lipedema (disease)", "Lipedema (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lipedema", "shortest_name_length": 8}
{"curie": "MONDO:0008143", "names": ["OA", "Oa", "OS1", "osteoarthrosis", "OSTEOARTHROSIS", "FRZB osteoarthritis", "OSTEOARTHRITIS SUSCEPTIBILITY 1", "osteoarthritis susceptibility 1", "osteoarthritis susceptibility type 1", "osteoarthritis caused by mutation in FRZB", "osteoarthritis of hip, female-specific, susceptibility to", "OSTEOARTHRITIS OF HIP, FEMALE-SPECIFIC, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteoarthritis susceptibility 1", "shortest_name_length": 2}
{"curie": "MONDO:0012133", "names": ["LATERAL SEMICIRCULAR CANAL MALFORMATION, FAMILIAL, WITH EXTERNAL AND MIDDLE EAR ABNORMALITIES", "lateral semicircular canal malformation, familial, with external and middle ear abnormalities", "Lateral semicircular canal malformation, familial, with external and middle ear abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lateral semicircular canal malformation, familial, with external and middle ear abnormalities", "shortest_name_length": 93}
{"curie": "MONDO:0005631", "names": ["boil", "Actinomycoses", "Actinomycosis", "Actinomycetes", "ACTINOMYCOSIS", "actinomycosis", "actinomycoses", "canaliculitis", "actinomycetoma", "Actinomycosis NOS", "Actinomycosis, NOS", "Keratoactinomycosis", "Actinomyces israeli", "actinomyces infection", "Actinomyces infection", "Actinomyces Infection", "Actinomycotic mycetema", "Infection, Actinomyces", "actinomycotic mycetema", "Actinomyces; infection", "infection; Actinomyces", "Actinomyces Infections", "infections, Actinomyces", "Actinomycotic infection", "actinomycotic infection", "Infections, Actinomyces", "Actinomycotic infections", "infection; actinomycotic", "actinomycotic; infection", "ACTINOMYCOTIC INFECTIONS", "actinomycosis (diagnosis)", "Actinomycotic madura foot", "actinomycotic madura foot", "Actinomycosis, unspecified", "Actinomycotic infection, NOS", "actinomycotic mycetoma of foot", "Actinomycotic mycetoma of foot", "Madura foot due to Actinomadura", "anaerobic Actinomyces infection", "Actinomycotic infectious disorders", "Actinomycotic infection (disorder)", "Actinomycotic infection of unspecified site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "actinomycosis", "shortest_name_length": 4}
{"curie": "MONDO:0017735", "names": ["Congenital narrowed aorta", "congenital aortic stenosis", "AORTIC STENOSIS CONGENITAL", "Congenital aortic stenosis", "aortic stenosis congenital", "Aortic stenosis congenital", "stenosis; aorta, congenital", "aorta; stenosis (congenital)", "Congenital stenosis of aorta", "Congenital stricture of aorta", "Congenital aortic stenosis NOS", "Aortic valve stenosis congenital", "congenital stenosis aortic valve", "congenital aortic valve stenosis", "Congenital aortic valve stenosis", "deformity; aortic valve, stenosis", "aortic valve; deformity, stenosis", "aortic valve; stenosis, congenital", "stenosis; aortic valve, congenital", "Congenital valvular aortic stenosis", "congenital valvular aortic stenosis", "Congenital stenosis of aortic valve", "aortic valve; stricture, congenital", "Congenital stenosis of aorta (disorder)", "congenital aortic valve stenosis (diagnosis)", "Congenital stenosis of aortic valve (disorder)", "Congenital valvular aortic stenosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital aortic valve stenosis", "shortest_name_length": 25}
{"curie": "MONDO:0022673", "names": ["CCP", "PCC", "cataract, polymorphic congenital", "Cataract, polymorphic congenital", "autosomal dominant non-nuclear cataract", "cataract congenital dominant non nuclear", "Cataract congenital dominant non nuclear", "Autosomal dominant nonnuclear polymorphic congenital cataract", "autosomal dominant nonnuclear polymorphic congenital cataract", "Cataract, Nonnuclear Polymorphic Congenital, Autosomal Dominant", "CATARACT, NONNUCLEAR POLYMORPHIC CONGENITAL, AUTOSOMAL DOMINANT", "cataract, Nonnuclear polymorphic congenital, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant non-nuclear cataract", "shortest_name_length": 3}
{"curie": "MONDO:0006558", "names": ["Gestational herpes", "Herpes Gestationis", "HERPES GESTATIONIS", "herpes gestationis", "Herpes gestationis", "gestational herpes", "gestational; herpes", "herpes; gestational", "pemphigus gestationis", "Pemphigoid Gestationi", "pemphigoid gestationis", "Gestationi, Pemphigoid", "Pemphigoid Gestationis", "gestational pemphigoid", "Gestational pemphigoid", "Pemphigoid gestationis", "Gestational Pemphigoid", "Gestationis, Pemphigoid", "Gestational Pemphigoids", "Pemphigoid, Gestational", "Pemphigoids, Gestational", "Herpes gestationis (disorder)", "herpes gestationis (diagnosis)", "Herpes gestationis NOS (disorder)", "Dermatitis herpetiformis of pregnancy", "Herpes gestationis unspecified (disorder)", "Herpes gestationis, unspecified trimester"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pemphigoid gestationis", "shortest_name_length": 18}
{"curie": "MONDO:0100104", "names": ["FADS4", "FETAL AKINESIA DEFORMATION SEQUENCE 4", "fetal akinesia deformation sequence 4", "fetal akinesia deformation sequence syndrome 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fetal akinesia deformation sequence 4", "shortest_name_length": 5}
{"curie": "MONDO:0001088", "names": ["Acute inferoposterior infarction", "acute inferoposterior infarction", "acute inferoposterior myocardial infarction", "acute myocardial infarction of inferoposterior wall", "Acute myocardial infarction of inferoposterior wall", "Acute myocardial infarction, of inferoposterior wall", "Acute myocardial infarction of inferoposterior wall (disorder)", "acute myocardial infarction of inferoposterior wall (diagnosis)", "Acute myocardial infarction of inferoposterior wall, episode of care unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute inferoposterior infarction", "shortest_name_length": 32}
{"curie": "MONDO:0019897", "names": ["monosomy 12qter", "distal deletion 12q", "distal monosomy 12q", "telomeric deletion 12q", "distal monosomy type 12q"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "distal monosomy 12q", "shortest_name_length": 15}
{"curie": "UMLS:C0042344", "names": ["stasis ulcer", "Stasis ulcer", "Venous Ulcer", "Stasis Ulcer", "Venous ulcer", "venous ulcer", "ulcer venous", "venous stasis", "Ulcer, stasis", "Ulcer, Stasis", "Venous stasis", "ulcers venous", "venous ulcers", "Ulcer, Venous", "ulcer; stasis", "Stasis Ulcers", "stasis; ulcer", "ulcers stasis", "stasis ulcers", "Venous Ulcers", "varicose ulcer", "Ulcer;varicose", "Varicose Ulcer", "Ulcers, Stasis", "ulcer varicose", "Ulcers, Venous", "Varicose ulcer", "ulcer; varicose", "varicose ulcers", "Ulcer, varicose", "varicose; ulcer", "Varicose Ulcers", "Ulcer, Varicose", "Stasis leg ulcer", "Venous ulcer NOS", "venous leg ulcer", "stasis leg ulcer", "Ulcers, Varicose", "venous ulceration", "Venous ulceration", "leg ulcers venous", "ulceration venous", "ulcerations venous", "venous stasis ulcer", "Venous stasis ulcer", "VARICOSE ULCERATION", "Gravitational ulcer", "Venous ulcer of leg", "Venous Stasis Ulcer", "VENOUS STASIS ULCER", "Varicose ulceration", "Venous Stasis Ulcers", "stasis ulcers venous", "stasis venous ulcers", "Ulcer, Venous Stasis", "venous stasis ulcers", "Stasis Ulcer, Venous", "Ulcers, Venous Stasis", "Stasis Ulcers, Venous", "Stasis pressure injury", "VARICOSE VEIN ULCERATED", "Ulcerated varicose veins", "ulcerated varicose veins", "Venous Hypertension Ulcer", "Venous Hypertension Ulcers", "Ulcer, Venous Hypertension", "Hypertension Ulcer, Venous", "Ulcers, Venous Hypertension", "Hypertension Ulcers, Venous", "venous stasis ulcer (diagnosis)", "Varicose veins (with ulceration)", "Stasis ulcer (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Varicose Ulcer", "shortest_name_length": 12}
{"curie": "MONDO:0044635", "names": ["DIAPH1-related sensorineural deafness-thrombocytopenia syndrome", "diaph1-related sensorineural hearing loss-thrombocytopenia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diaph1-related sensorineural hearing loss-thrombocytopenia syndrome", "shortest_name_length": 63}
{"curie": "UMLS:C4288404", "names": ["Peritoneal DSRCT", "Peritoneal Desmoplastic Small Round Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peritoneal Desmoplastic Small Round Cell Tumor", "shortest_name_length": 16}
{"curie": "UMLS:C0549609", "names": ["DYSFUNCTION ADRENAL", "Dysfunction adrenal", "ADRENAL DYSFUNCTION", "adrenal dysfunction", "dysfunction; adrenal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dysfunction adrenal", "shortest_name_length": 19}
{"curie": "MONDO:0002479", "names": ["Androblastoma", "Androblastomas", "Arrhenoblastoma", "Arrhenoblastomas", "Sertoli-Leydig Cell Tumor", "Sertoli Leydig Cell Tumor", "Sertoli-Leydig cell tumor", "sertoli-leydig cell tumor", "sertoli leydig cell tumor", "Sertoli-Leydig cell tumour", "Sertoli Leydig Cell Tumors", "Sertoli-Leydig Cell Tumors", "Tumor, Sertoli-Leydig Cell", "Cell Tumor, Sertoli-Leydig", "Tumors, Sertoli-Leydig Cell", "Cell Tumors, Sertoli-Leydig"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sertoli-Leydig cell tumor", "shortest_name_length": 13}
{"curie": "UMLS:C0235814", "names": ["NEUROFIBROMATOSIS AGGRAVATED", "Aggravated Neurofibromatosis", "Neurofibromatosis aggravated", "Neurofibromatosis Aggravated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neurofibromatosis aggravated", "shortest_name_length": 28}
{"curie": "MONDO:0012988", "names": ["HH6", "KAL6", "Kallmann syndrome 6", "Kallmann Syndrome 6", "FGF8 hypogonadotropic hypogonadism", "hypogonadotropic hypogonadism 6 with or without anosmia", "HYPOGONADOTROPIC HYPOGONADISM 6 WITH OR WITHOUT ANOSMIA", "hypogonadotropic hypogonadism caused by mutation in FGF8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadotropic hypogonadism 6 with or without anosmia", "shortest_name_length": 3}
{"curie": "MONDO:0004635", "names": ["postcricoid region cancer", "Malignant Postcricoid Tumor", "malignant postcricoid tumor", "malignant Postcricoid tumor", "Malignant Postcricoid Neoplasm", "malignant postcricoid neoplasm", "Malignant Tumor of Postcricoid Area", "malignant tumor of postcricoid area", "Malignant tumor of postcricoid region", "malignant neoplasm of postcricoid area", "Malignant Neoplasm of Postcricoid Area", "Malignant tumour of postcricoid region", "malignant tumor of the postcricoid area", "Malignant Tumor of the Postcricoid Area", "Malignant neoplasm of postcricoid region", "Malignant Neoplasm of the Postcricoid Area", "malignant neoplasm of the postcricoid area", "Malignant tumor of pharyngoesophageal junction", "malignant tumor of pharyngoesophageal junction", "Malignant tumor of pharyngo-esophageal junction", "Malignant tumor of postcricoid region (disorder)", "Malignant tumour of pharyngo-oesophageal junction", "malignant hypopharyngeal neoplasm of postcricoid region", "Malignant neoplasm of postcricoid region of hypopharynx", "malignant hypopharyngeal neoplasm of postcricoid region (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postcricoid region cancer", "shortest_name_length": 25}
{"curie": "UMLS:C1879643", "names": ["Adult Granulosa Cell Tumor", "Adult granulosa cell tumor", "Adult Type Granulosa Cell Tumor", "Granulosa cell tumor, adult type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Type Granulosa Cell Tumor", "shortest_name_length": 26}
{"curie": "MONDO:0000662", "names": ["Amusia", "amusia", "Amusia, NOS", "Amusia (finding)", "receptive amusia", "amusia (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amusia", "shortest_name_length": 6}
{"curie": "MONDO:0005111", "names": ["EBV infection", "EBV INFECTION", "EBV Infection", "infection ebv", "ebv infection", "EBV infections", "EBV Infections", "Infection, EBV", "Infections, EBV", "infections, EBV", "Epstein-Barr Virus", "EPSTEIN BARR INFECTION", "epstein barr infection", "barr epstein infections", "Epstein-Barr virus disease", "Epstein-Barr virus diseases", "Epstein-Barr Virus Infection", "epstein-barr virus infection", "EPSTEIN BARR VIRUS INFECTION", "epstein barr virus infection", "Epstein-Barr virus infection", "epstein-barr infection virus", "Epstein Barr Virus Infection", "epstein barr infection viral", "Epstein-Barr Virus infection", "infection epstein-barr virus", "Epstein Barr Virus infection", "human herpesvirus 4 infection", "Epstein-Barr viral infections", "Virus Infection, Epstein-Barr", "virus infections barr epstein", "Infection, Epstein-Barr Virus", "Epstein Barr Virus Infections", "Epstein-Barr Virus Infections", "Epstein Barr Virus infections", "infections, Epstein-Barr Virus", "Human Herpesvirus 4 Infections", "Virus infections, Epstein-Barr", "Virus Infections, Epstein-Barr", "Human Herpesvirus 4 infections", "Infections, Epstein-Barr Virus", "Herpesvirus 4 infections, Human", "Human Herpes Virus 4 infections", "Human Herpes Virus 4 Infections", "Herpesvirus 4 Infections, Human", "Epstein-Barr virus disease (disorder)", "human herpesvirus 4 infection (diagnosis)", "Human gammaherpesvirus 4 infectious disease", "Human gammaherpesvirus 4 disease or disorder", "Human gammaherpesvirus 4 caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epstein-Barr virus infection", "shortest_name_length": 13}
{"curie": "MONDO:0030434", "names": ["EIG18", "epilepsy, idiopathic generalized, susceptibility to, 18", "EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 18"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, idiopathic generalized, susceptibility to, 18", "shortest_name_length": 5}
{"curie": "MONDO:0015232", "names": ["radial deficiency-tibial hypoplasia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radial deficiency-tibial hypoplasia syndrome", "shortest_name_length": 44}
{"curie": "UMLS:C0851302", "names": ["Insulin shock", "SHOCK HYPOGLYCEMIC", "Hypoglycemic shock", "hypoglycemic shock", "Shock hypoglycemic", "Hypoglycaemic shock", "Shock hypoglycaemic", "hypoglycaemic shock", "Hypoglycemic shock NOS", "Hypoglycemic shock (disorder)", "hypoglycemic shock (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypoglycemic shock", "shortest_name_length": 13}
{"curie": "MONDO:0005068", "names": ["MI", "mi", "AMI", "mies", "Heart Attack", "heart attack", "HEART ATTACK", "Heart attack", "heart attacks", "attack hearts", "Heart Attacks", "attacks hearts", "Cardiac infarct", "attacking heart", "ATTACK CORONARY", "coronary attack", "Attack coronary", "attacks coronary", "heart infarction", "Infarction;heart", "HEART INFARCTION", "Heart attack, NOS", "Attack heart (NOS)", "Cardiac infarction", "INFARCT MYOCARDIAL", "myocardial infarct", "cardiac infarction", "MYOCARDIAL INFARCT", "Myocardial Infarct", "Infarct myocardial", "Myocardial infarct", "ATTACK HEART (NOS)", "myocardial infarcts", "Infarct, Myocardial", "infarcts myocardial", "Myocardial Infarcts", "cardiac; infarction", "myocardial necrosis", "Infarction of heart", "Infarcts, Myocardial", "MYOCARDIAL INFARCTION", "Myocardial infarction", "Infarction;myocardial", "Myocardial Infarction", "myocardial infarction", "Cardiovascular Stroke", "myocardial infarctions", "Infarction, Myocardial", "Stroke, Cardiovascular", "Cardiovascular Strokes", "Myocardial Infarctions", "infarction; myocardial", "infarctions myocardial", "Infarctions, Myocardial", "Strokes, Cardiovascular", "Cardiac infarction, NOS", "Infarctions (Myocardial)", "Infarction of heart, NOS", "MI, myocardial infarction", "Myocardial infarction NOS", "MI - myocardial infarction", "MI - Myocardial infarction", "Myocardial infarction (MI)", "Myocardial infarction, NOS", "infarction (MI), myocardial", "myocardial infarction, (MI)", "Right ventricular infarction", "Myocardial infarction syndrome", "disorder infarction myocardial", "syndrome myocardial infarction", "myocardial infarction (disease)", "Myocardial infarction (disorder)", "myocardial infarction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myocardial infarction", "shortest_name_length": 2}
{"curie": "MONDO:0006340", "names": ["ovary serous adenofibroma", "Ovarian Serous Adenofibroma", "ovarian serous adenofibroma", "serous adenofibroma of ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian serous adenofibroma", "shortest_name_length": 25}
{"curie": "UMLS:C3146245", "names": ["ADENOMATOUS STOMACH POLYP", "gastric adenomatous polyp", "Gastric Adenomatous Polyp", "adenomatous polyp of stomach", "Gastric Adenoma, Intestinal-Type", "adenomatous polyp of stomach (diagnosis)", "Gastric Adenomatous Polyp, Intestinal-Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenomatous polyp of stomach", "shortest_name_length": 25}
{"curie": "UMLS:C0475059", "names": ["Traumatic Subdural Hematoma", "SUBDURAL HEMATOMA TRAUMATIC", "traumatic subdural hematoma", "Traumatic subdural hematoma", "Traumatic subdural haematoma", "Haematoma;subdural;traumatic", "Hematoma, Traumatic Subdural", "Traumatic Subdural Hematomas", "traumatic subdural haematoma", "Subdural Hematoma, Traumatic", "Hematomas, Traumatic Subdural", "subdural hematoma - traumatic", "Subdural Hematomas, Traumatic", "Subdural hematoma (traumatic)", "Subdural haematoma (traumatic)", "Traumatic subdural hematoma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subdural Hematoma, Traumatic", "shortest_name_length": 27}
{"curie": "UMLS:C2827981", "names": ["Stage IB Breast Cancer", "stage IB breast cancer", "breast cancer, stage IB", "Stage IB Breast Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Breast Cancer AJCC v7", "shortest_name_length": 22}
{"curie": "UMLS:C3282903", "names": ["Metastatic Carcinoma to the Liver", "Metastatic Carcinoma in the Liver"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Carcinoma in the Liver", "shortest_name_length": 33}
{"curie": "MONDO:0002944", "names": ["external ear carcinoma", "External Ear Carcinoma", "external Ear carcinoma", "carcinoma of external ear", "carcinoma of external Ear", "Carcinoma of External Ear", "carcinoma of the External ear", "carcinoma of the external ear", "carcinoma of the external Ear", "Carcinoma of the External Ear"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "external ear carcinoma", "shortest_name_length": 22}
{"curie": "MONDO:0012590", "names": ["XFEPS", "XFE Progeroid Syndrome", "XFE PROGEROID SYNDROME", "XFE progeroid syndrome", "XPF-ERCC1 Progeroid Syndrome", "XPF-ERCC1 progeroid syndrome", "XPF-ERCC1 PROGEROID SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "XFE progeroid syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0100373", "names": ["AML, inv(16)(p13q22)", "AML, inv(16)(p13;q22)", "AML, inv(16)(p13.1q22)", "AML, inv(16)(p13.1;q22)", "AML, inv(16)(p13.1q22.1)", "AML, inv(16)(p13.1;q22.1)", "Acute Myeloid Leukemia, inv(16)(p13q22)", "Acute myeloid leukemia, inv(16)(p13;q22)", "acute myeloid leukemia, inv(16)(p13.1;q22)", "Acute Myeloid Leukemia with inv(16)(p13q22)", "Acute Myeloid Leukemia with inv(16)(p13q22)(CBFb/MYH11)", "Acute Myeloid Leukemia with inv(16)(p13.1q22); CBFB-MYH11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, inv(16)(p13.1;q22)", "shortest_name_length": 20}
{"curie": "MONDO:0007082", "names": ["AA1", "alopecia areata 1", "Alopecia Areata 1", "ALOPECIA AREATA 1", "alopecia universalis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alopecia areata 1", "shortest_name_length": 3}
{"curie": "MONDO:0009218", "names": ["FRBRL", "Farber", "AC deficiency", "AC DEFICIENCY", "FARBER DISEASE", "Farber disease", "Farber Disease", "farber disease", "Farbers Disease", "disease farbers", "disease farber s", "farber's disease", "Farber's Disease", "Farber's disease", "Disease, Farber's", "Farber's Diseases", "Diseases, Farber's", "CERAMIDASE DEFICIENCY", "Farber-Uzman syndrome", "Ceramidase Deficiency", "Ceramidase deficiency", "ceramidase deficiency", "Deficiency, Ceramidase", "Ceramidase Deficiencies", "Deficiencies, Ceramidase", "FARBER LIPOGRANULOMATOSIS", "Farber lipogranulomatosis", "Farber Lipogranulomatosis", "acid ceramidase deficiency", "Acid Ceramidase Deficiency", "Lipogranulomatosis, Farber", "Acid ceramidase deficiency", "ACID CERAMIDASE DEFICIENCY", "Ceramidase Deficiency, Acid", "farber's lipogranulomatosis", "Farber's lipogranulomatosis", "Deficiency, Acid Ceramidase", "Acid Ceramidase Deficiencies", "Disseminated lipogranulomatosis", "Acylsphingosine deacylase deficiency", "Farber lipogranulomatosis (diagnosis)", "Farber's lipogranulomatosis (disorder)", "N-Laurylsphingosine Deacylase Deficiency", "N-Laurylsphingosine deacylase deficiency", "N-LAURYLSPHINGOSINE deacylase deficiency", "N-laurylsphingosine deacylase deficiency", "N Laurylsphingosine Deacylase Deficiency", "N-LAURYLSPHINGOSINE DEACYLASE DEFICIENCY", "Deficiency, N-Laurylsphingosine Deacylase", "N-Laurylsphingosine Deacylase Deficiencies", "Deficiencies, N-Laurylsphingosine Deacylase"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Farber lipogranulomatosis", "shortest_name_length": 5}
{"curie": "MONDO:0013829", "names": ["UVSS2", "UV-SENSITIVE SYNDROME 2", "UV-Sensitive Syndrome 2", "UV-sensitive syndrome 2", "ERCC8 UV-sensitive syndrome", "UV-sensitive syndrome type 2", "UV-sensitive syndrome caused by mutation in ERCC8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "UV-sensitive syndrome 2", "shortest_name_length": 5}
{"curie": "UMLS:C0392154", "names": ["ABSCESS EYE", "Abscess eye", "eye abscess", "Eye abscess", "eye; abscess", "abscesses eye", "abscess of eye", "Abscess of eye", "Abscess of eye (disorder)", "abscess of eye (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abscess of eye", "shortest_name_length": 11}
{"curie": "MONDO:0009381", "names": ["hyperbilirubinemia, conjugated, type 3", "Hyperbilirubinemia, Conjugated, Type III", "hyperbilirubinemia, conjugated, type III", "HYPERBILIRUBINEMIA, CONJUGATED, TYPE III", "Hyperbilirubinemia - conjugated - type III", "Hyperbilirubinaemia - conjugated - type III", "Hyperbilirubinemia - conjugated - type III (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperbilirubinemia, conjugated, type 3", "shortest_name_length": 38}
{"curie": "MONDO:0000213", "names": ["autoimmune disease, multisystem, infantile-onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune disease, multisystem, infantile-onset", "shortest_name_length": 48}
{"curie": "MONDO:0002915", "names": ["pediatric infratentorial tumor", "Pediatric Infratentorial Tumor", "pediatric Infratentorial tumor", "childhood infratentorial tumor", "Childhood Infratentorial Tumor", "childhood infratentorial tumors", "Childhood Infratentorial Tumors", "Pediatric Infratentorial Neoplasm", "Childhood Infratentorial Neoplasm", "childhood infratentorial neoplasm", "pediatric infratentorial neoplasm", "Childhood Infratentorial Neoplasms", "childhood infratentorial neoplasms", "infratentorial neoplasm of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood infratentorial neoplasm", "shortest_name_length": 30}
{"curie": "MONDO:0007688", "names": ["MYHRS", "Laps Syndrome", "LAPS syndrome", "LAPS SYNDROME", "MYHRE SYNDROME", "Myhre Syndrome", "Myhre syndrome", "MYHRE syndrome", "Myhre syndrome (disorder)", "Myhre syndrome (diagnosis)", "Growth-mental deficiency syndrome of Myhre", "Growth mental deficiency syndrome of Myhre", "GROWTH-MENTAL DEFICIENCY SYNDROME OF MYHRE", "Laryngotracheal stenosis, arthropathy, prognathism and short stature", "Laryngotracheal Stenosis, Arthropathy, Prognathism, and Short Stature", "laryngotracheal stenosis, arthropathy, prognathism, and short stature", "LARYNGOTRACHEAL STENOSIS, ARTHROPATHY, PROGNATHISM, AND SHORT STATURE", "Facial dysmorphism, intellectual deficit, short stature and hearing loss", "facial dysmorphism - intellectual deficit - short stature - hearing loss", "Facial dysmorphism-intellectual disability-short stature-deafness syndrome", "facial dysmorphism-intellectual disability-short stature-hearing loss syndrome", "Facial dysmorphism-intellectual disability-short stature-hearing loss syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myhre syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C1368355", "names": ["SYNOSTOSIS", "Synostosis", "Synostosis malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Synostosis malformation", "shortest_name_length": 10}
{"curie": "UMLS:C0033797", "names": ["Pseudodementia", "pseudodementia", "Pseudodementia (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pseudodementia", "shortest_name_length": 14}
{"curie": "MONDO:0008886", "names": ["Sabinas syndrome", "trichothiodystrophy type B", "SABINAS BRITTLE HAIR SYNDROME", "Sabinas brittle hair syndrome", "BRITTLE HAIR AND MENTAL DEFICIT", "brittle hair and mental Deficit", "Brittle hair and mental deficit", "brittle hair syndrome, Sabinas type", "brittle hair-mental deficit syndrome", "brittle hair-mental deficiency syndrome", "Sabinas brittle hair syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sabinas brittle hair syndrome", "shortest_name_length": 16}
{"curie": "UMLS:C0854456", "names": ["gangrene cellulitis", "Gangrenous cellulitis", "Cellulitis gangrenous", "gangrenous; cellulitis", "cellulitis; gangrenous", "gangrene cellulitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gangrenous cellulitis", "shortest_name_length": 19}
{"curie": "MONDO:0011342", "names": ["CDG2F", "CDGIIf", "CDGIIF", "CDG-IIf", "CDG IIF", "CDG IIf", "CDGIIdf", "SLC35A1-CDG", "SLC35A1-CDG (CDG-IIf)", "CDG syndrome type IIf", "CMP-sialic acid transporter deficiency", "congenital disorder of glycosylation type 2f", "SLC35A1 congenital disorder of glycosylation", "Congenital disorder of glycosylation type 2f", "SLC35A1-congenital disorder of glycosylation", "congenital disorder of glycosylation type IIf", "Congenital disorder of glycosylation type IIf", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIf", "congenital disorder of glycosylation, type IIf", "Congenital Disorder Of Glycosylation, Type IIF", "Carbohydrate deficient glycoprotein syndrome type IIf", "carbohydrate deficient glycoprotein syndrome type IIf", "Solute carrier family 35 member A1 congenital disorder of glycosylation", "SLC35A1 (solute carrier family 35 member A1) congenital disorder of glycosylation", "Solute carrier family 35 member A1 congenital disorder of glycosylation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SLC35A1-congenital disorder of glycosylation", "shortest_name_length": 5}
{"curie": "MONDO:0022057", "names": ["CEOT", "Pindborg", "Pindborg tumor", "Pindborg Tumor", "tumor; Pindborg", "Pindborg tumour", "Pindborg; tumor", "Calcifying epithelial odontogenic tumor", "calcifying epithelial odontogenic tumor", "Calcifying Epithelial Odontogenic Tumor", "Calcifying epithelial odontogenic tumour", "calcifying; odontogenic epithelial tumor", "tumor; calcifying epithelial odontogenic", "tumor; odontogenic, calcifying epithelial", "odontogenic; tumor, calcifying epithelial", "epithelial; tumor, calcifying, odontogenic", "calcifying; epithelial neoplasm, odontogenic", "CEOT - Calcifying epithelial odontogenic tumor", "CEOT - Calcifying epithelial odontogenic tumour", "Calcifying epithelial odontogenic tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "calcifying epithelial odontogenic tumor", "shortest_name_length": 4}
{"curie": "UMLS:C1274594", "names": ["Lichenoid Keratosis", "lichenoid keratosis", "Lichenoid keratosis", "Lichenoid actinic keratosis", "lichenoid actinic keratosis", "Lichen planus-like keratosis", "Lichen Planus-Like Keratosis", "Lichenoid actinic keratosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lichenoid actinic keratosis", "shortest_name_length": 19}
{"curie": "MONDO:0032691", "names": ["GAMOS6", "Galloway-Mowat syndrome 6", "GALLOWAY-MOWAT SYNDROME 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Galloway-Mowat syndrome 6", "shortest_name_length": 6}
{"curie": "UMLS:C1367534", "names": ["Cellular Angiofibroma", "Cellular angiofibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cellular angiofibroma", "shortest_name_length": 21}
{"curie": "UMLS:C1262004", "names": ["Embolic cerebral infarction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Embolic cerebral infarction", "shortest_name_length": 27}
{"curie": "UMLS:C3899153", "names": ["Fat adherence syndrome", "Fat Adherence Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fat adherence syndrome", "shortest_name_length": 22}
{"curie": "UMLS:C4086165", "names": ["Neuroblastoma", "Childhood Neuroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Neuroblastoma", "shortest_name_length": 13}
{"curie": "UMLS:C0343243", "names": ["Muscle abscess", "muscle abscess", "muscle; abscess", "abscess; muscle", "abscesses muscle", "Muscle abscess (disorder)", "muscle abscess (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Muscle abscess", "shortest_name_length": 14}
{"curie": "MONDO:0008821", "names": ["arthrogryposis, distal, with mental retardation and characteristic facies", "Arthrogryposis, Distal, with Mental Retardation and Characteristic Facies", "ARTHROGRYPOSIS, DISTAL, WITH MENTAL RETARDATION AND CHARACTERISTIC FACIES", "arthrogryposis, distal, with intellectual disability and characteristic facies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis, distal, with intellectual disability and characteristic facies", "shortest_name_length": 73}
{"curie": "UMLS:C1336002", "names": ["Small Intestinal Low-Grade Dysplasia", "Small Intestinal Low Grade Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Intestinal Low Grade Intraepithelial Neoplasia", "shortest_name_length": 36}
{"curie": "MONDO:0015060", "names": ["mosaic trisomy 3", "Mosaic trisomy 3", "Trisomy 3 mosaicism", "trisomy 3 mosaicism", "Mosaic trisomy type 3", "Mosaic trisomy 3 syndrome", "Mosaic trisomy chromosome 3", "Mosaic trisomy 3 syndrome (disorder)", "Mosaic trisomy 3 syndrome (diagnosis)", "anomaly of chromosome pair mosaic trisomy 3 syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mosaic trisomy 3", "shortest_name_length": 16}
{"curie": "MONDO:0022803", "names": ["coloboma porencephaly hydronephrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coloboma porencephaly hydronephrosis", "shortest_name_length": 36}
{"curie": "UMLS:C0857468", "names": ["Withdrawal hypertension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Withdrawal hypertension", "shortest_name_length": 23}
{"curie": "OMIM:247420", "names": ["LUTHERAN NULL", "LuLu phenotype", "LuLu phenotype (finding)", "Recessive Lu(a-b-) phenotype", "RECESSIVE LU (a-b-) PHENOTYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 13}
{"curie": "UMLS:C3146255", "names": ["Stage IV Rectal Cancer", "Stage IV Rectal Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Rectal Cancer AJCC v7", "shortest_name_length": 22}
{"curie": "MONDO:0017436", "names": ["LCCS", "lethal congenital contracture syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal congenital contracture syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C4050175", "names": ["CHR", "Complete Hematologic Response"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Complete Hematologic Response", "shortest_name_length": 3}
{"curie": "MONDO:0009578", "names": ["NCM", "NCMS", "Neuromelanosis", "NEUROMELANOSIS", "melanosis neurocutaneous", "Neurocutaneous melanosis", "Neurocutaneous Melanosis", "neurocutaneous melanosis", "MELANOSIS, NEUROCUTANEOUS", "Melanosis, neurocutaneous", "melanosis, neurocutaneous", "Neurocutaneous melanocytosis", "Neurocutaneous Melanocytosis", "neurocutaneous melanocytosis", "neurocutaneous melanosis, somatic", "neurocutaneous melanosis syndrome", "Neurocutaneous melanosis syndrome", "Neurocutaneous melanosis (disorder)", "neurocutaneous melanocytosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurocutaneous melanocytosis", "shortest_name_length": 3}
{"curie": "UMLS:C0030167", "names": ["Pachymeningitis", "pachymeningitis", "Pachymeningitides", "pachymeningitides", "pachymeningitis NOS", "Pachymeningitis, NOS", "Pachymeningitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pachymeningitis", "shortest_name_length": 15}
{"curie": "MONDO:0008828", "names": ["CACP", "PAC syndrome", "PAC SYNDROME", "CAP SYNDROME", "CAP syndrome", "CACP syndrome", "Jacobs syndrome", "JACOBS SYNDROME", "familial fibrosing serositis", "Fibrosing serositis, familial", "fibrosing serositis, familial", "FIBROSING SEROSITIS, FAMILIAL", "Arthropathy camptodactyly syndrome", "arthropathy camptodactyly syndrome", "ARTHROPATHY-CAMPTODACTYLY SYNDROME", "Arthropathy-Camptodactyly Syndrome", "arthropathy-camptodactyly syndrome", "Arthropathy-camptodactyly syndrome", "Congenital familial hypertrophic synovitis", "congenital familial hypertrophic synovitis", "HYPERTROPHIC SYNOVITIS, CONGENITAL FAMILIAL", "hypertrophic synovitis, congenital familial", "Hypertrophic Synovitis, Congenital Familial", "pericarditis-arthropathy-camptodactyly syndrome", "Camptodactyly arthropathy pericarditis syndrome", "Pericarditis arthropathy camptodactyly syndrome", "pericarditis arthropathy camptodactyly syndrome", "Camptodactyly-Arthropathy-Pericarditis Syndrome", "PERICARDITIS-ARTHROPATHY-CAMPTODACTYLY SYNDROME", "Pericarditis-Arthropathy-Camptodactyly Syndrome", "camptodactyly arthropathy pericarditis syndrome", "Pericarditis-arthropathy-camptodactyly syndrome", "camptodactyly-arthropathy-pericarditis syndrome", "CAMPTODACTYLY-ARTHROPATHY-PERICARDITIS SYNDROME", "Pericarditis, arthropathy, camptodactyly syndrome", "Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome", "CAMPTODACTYLY-ARTHROPATHY-COXA VARA-PERICARDITIS SYNDROME", "camptodactyly arthropathy coxa vara pericarditis syndrome", "Camptodactyly-arthropathy-coxa vara-pericarditis syndrome", "camptodactyly-arthropathy-coxa-vara-pericarditis syndrome", "camptodactyly-arthropathy-coxa vara-pericarditis syndrome", "Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome", "CACP (camptodactyly, arthropathy, coxa-vara, pericarditis) syndrome", "Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "camptodactyly-arthropathy-coxa vara-pericarditis syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C2981386", "names": ["Stage IIB Appendix Cancer", "Stage IIB Appendix Carcinoma", "Stage IIB Appendix Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Appendix Carcinoma AJCC v7", "shortest_name_length": 25}
{"curie": "MONDO:0024501", "names": ["vermiform appendix NET", "appendix neuroendocrine neoplasm", "Appendix Neuroendocrine Neoplasm", "vermiform appendix neuroendocrine tumor", "vermiform appendix neuroendocrine neoplasm", "neuroendocrine neoplasm of vermiform appendix", "vermiform appendix neuroendocrine tumor, well differentiated, low or intermediate grade"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "appendix neuroendocrine neoplasm", "shortest_name_length": 22}
{"curie": "MONDO:0024487", "names": ["NAIL INFECTION", "Nail Infection", "infection nail", "Nail infection", "nail infection", "nails infection", "nail; infection", "infections nail", "Nail infections", "infection nails", "infection; nail", "infections nails", "Infection of nail", "Infection;nail(s)", "Nail infection NOS", "Infection of nail NOS", "Nail infection (diagnosis)", "Infection of nail (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nail infection", "shortest_name_length": 14}
{"curie": "UMLS:C4526831", "names": ["Bone Cancer by AJCC v8 Stage", "Appendicular Skeleton, Trunk, Skull, and Facial Bones Cancer by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone Cancer by AJCC v8 Stage", "shortest_name_length": 28}
{"curie": "MONDO:0013063", "names": ["VF2", "DPP6 ventricular fibrillation (disease)", "Ventricular Fibrillation, Paroxysmal Familial, 2", "ventricular fibrillation, paroxysmal familial, 2", "VENTRICULAR FIBRILLATION, PAROXYSMAL FAMILIAL, 2", "ventricular fibrillation, paroxysmal familial, type 2", "ventricular fibrillation (disease) caused by mutation in DPP6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ventricular fibrillation, paroxysmal familial, 2", "shortest_name_length": 3}
{"curie": "UMLS:C3532496", "names": ["Orocutaneous fistula", "Orocutaneous Fistula", "Orocutaneous fistula (disorder)", "Fistula between oral cavity and cutaneous surface of face"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Orocutaneous fistula", "shortest_name_length": 20}
{"curie": "UMLS:C0347804", "names": ["Acetabular Fracture", "Acetabular fracture", "fracture acetabulum", "Acetabulum Fracture", "fracture acetabular", "acetabulum fracture", "Acetabulum fracture", "acetabular fracture", "acetabulum; fracture", "acetabulum fractures", "fracture; acetabulum", "acetabular fractures", "Fracture of acetabulum", "fracture of acetabulum", "pelvic fracture acetabulum", "Fracture of acetabulum, NOS", "Fracture of acetabulum (disorder)", "fracture of acetabulum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fracture of acetabulum", "shortest_name_length": 19}
{"curie": "MONDO:0001789", "names": ["SPINE NEUROFIBROMA", "Spinal Cord Neurofibroma", "spinal cord neurofibroma", "Neurofibroma of Spinal Cord", "neurofibroma of spinal cord"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurofibroma of spinal cord", "shortest_name_length": 18}
{"curie": "UMLS:C1739372", "names": ["Acute graft versus host disease in skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute graft versus host disease in skin", "shortest_name_length": 39}
{"curie": "MONDO:0012210", "names": ["Mgr7", "MGR7", "MIGRAINE WITH AURA, SUSCEPTIBILITY TO, 7", "migraine with aura, susceptibility to, 7", "migraine with aura, susceptibility to, type 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "migraine with aura, susceptibility to, 7", "shortest_name_length": 4}
{"curie": "MONDO:0010370", "names": ["CDLS2", "CdLS2", "X-Linked CdLS", "X-Linked CdLSs", "Cdls, X-linked", "CdLS, X Linked", "CdLS, X-Linked", "CDLS, X-LINKED", "CdLSs, X-Linked", "Lange syndrome 2", "de Lange syndrome 2", "Bruch-de Lange syndrome", "Bruck-de Lange syndrome", "Cornelia de Lange Syndrome 2", "Cornelia DE Lange syndrome 2", "Cornelia de Lange syndrome 2", "CORNELIA DE LANGE SYNDROME 2", "SMC1A Cornelia de Lange syndrome", "Cornelia De Lange syndrome type 2", "Cornelia de Lange syndrome (CLS) 2", "X-Linked Cornelia De Lange Syndrome", "X-linked Cornelia De Lange syndrome", "Cornelia De Lange syndrome, X-linked", "CORNELIA DE LANGE SYNDROME, X-LINKED", "Cornelia de Lange Syndrome, X-Linked", "Cornelia de Lange Syndrome, X Linked", "Cornelia de Lange syndrome 2, X-linked dominant", "Congenital muscular hypertrophy-cerebral syndrome", "congenital muscular hypertrophy-cerebral syndrome", "Cornelia de Lange syndrome caused by mutation in SMC1A", "Congenital muscular hypertrophy-cerebral syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cornelia de Lange syndrome 2", "shortest_name_length": 5}
{"curie": "UMLS:C1334008", "names": ["High Grade Sarcoma", "High-Grade Sarcoma", "Poorly Differentiated or Undifferentiated Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "High Grade Sarcoma", "shortest_name_length": 18}
{"curie": "UMLS:C4055261", "names": ["Chemotherapeutic Drug - Induced Nephropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chemotherapeutic Drug - Induced Nephropathy", "shortest_name_length": 43}
{"curie": "MONDO:0024330", "names": ["AOM", "otitis media", "Otitis media", "acute media otitis", "Acute Otitis Media", "acute otitis Media", "otitis media acute", "Acute otitis media", "Otitis media;acute", "acute otitis media", "Otitis media acute", "OTITIS MEDIA ACUTE", "middle Ear infection", "otitis; media, acute", "Middle Ear Infection", "Otitis media acute NOS", "Acute otitis media NOS", "infectious otitis Media", "Acute otitis media, NOS", "infectious otitis media", "Infectious Otitis Media", "AOM - Acute otitis media", "Acute middle ear infection", "Acute otitis media (disorder)", "acute otitis media (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infectious otitis media", "shortest_name_length": 3}
{"curie": "UMLS:C5446588", "names": ["Locally Advanced Small Intestinal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Small Intestinal Adenocarcinoma", "shortest_name_length": 48}
{"curie": "UMLS:C0750197", "names": ["Sustained VT", "sustained tachycardia ventricular", "sustained ventricular tachycardia", "Sustained ventricular tachycardia", "Sustained Ventricular Tachycardia", "VENTRICULAR TACHYCARDIA SUSTAINED", "SUSTAINED VENTRICULAR TACHYCARDIA", "Ventricular Tachycardia, Sustained", "Sustained ventricular tachycardia (disorder)", "Sustained Ventricular Tachycardia by ECG Finding", "Sustained Ventricular Tachycardia by EKG Finding"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sustained ventricular tachycardia", "shortest_name_length": 12}
{"curie": "UMLS:C0854752", "names": ["Gastric cancer stage IV with metastases", "Stomach cancer stage IV with metastases", "Stage IV Gastric Cancer with Metastasis", "Stage IV Gastric Carcinoma with Metastasis", "Gastric malignancy stage IV with metastases", "Malignant neoplasm of stomach stage IV with metastases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Gastric Cancer with Metastasis", "shortest_name_length": 39}
{"curie": "MONDO:0011828", "names": ["MRT2", "MRT2A", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 2", "Mental Retardation, Autosomal Recessive 2", "mental retardation, autosomal recessive 2", "mental retardation, autosomal recessive 2A", "Mental Retardation, Autosomal Recessive 2A", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 2A", "intellectual disability, autosomal recessive 2", "mental retardation, autosomal recessive type 2", "intellectual disability, autosomal recessive 2A", "intellectual disability, autosomal recessive type 2", "autosomal recessive intellectual developmental disorder 2", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 2", "CRBN autosomal recessive non-syndromic intellectual disability", "autosomal recessive non-syndromic intellectual disability caused by mutation in CRBN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 2", "shortest_name_length": 4}
{"curie": "UMLS:C0281700", "names": ["Stage I Burkitt Lymphoma", "Stage I Childhood Burkitt Lymphoma", "Stage I Childhood Burkitt's Lymphoma", "Ann Arbor Stage I Childhood Burkitt Lymphoma", "stage I childhood small noncleaved cell lymphoma", "Stage I Pediatric Small Non-Cleaved Cell Lymphoma", "Stage I Childhood Small Non-Cleaved Cell Lymphoma", "childhood small noncleaved cell lymphoma, stage I", "Childhood Small Non-Cleaved Cell Lymphoma Stage I", "lymphoma, stage I childhood small noncleaved cell", "stage I small noncleaved cell lymphoma, childhood", "Pediatric Small Non-Cleaved Cell Lymphoma Stage I", "pediatric small noncleaved cell lymphoma, stage I", "small noncleaved cell lymphoma, childhood, stage I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Childhood Burkitt Lymphoma", "shortest_name_length": 24}
{"curie": "MONDO:0001305", "names": ["larynx stenosis", "laryngostenosis", "Laryngostenoses", "stenosis larynx", "Laryngostenosis", "larynx; stenosis", "Larynx--Stenosis", "stenosis; larynx", "narrowing; larynx", "larynx; stricture", "larynx; narrowing", "stricture; larynx", "stenosis of larynx", "Stenosis of larynx", "LARYNGEAL STENOSIS", "Laryngeal Stenoses", "Laryngeal Stenosis", "Laryngeal stenosis", "laryngeal stenosis", "Stenoses, Laryngeal", "laryngeal stricture", "Laryngeal stricture", "Stenosis, Laryngeal", "Stenosis of larynx (disorder)", "stenosis of larynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laryngostenosis", "shortest_name_length": 15}
{"curie": "MONDO:0017415", "names": ["EVMPS", "Escobar syndrome", "Escobar Syndrome", "escobar syndrome", "ESCOBAR SYNDROME", "Pterygium syndrome", "PTERYGIUM SYNDROME", "pterygium syndrome", "pterygium universale", "PTERYGIUM UNIVERSALE", "Pterygium universale", "pterygium colli syndrome", "Pterygium colli syndrome", "PTERYGIUM COLLI SYNDROME", "Multiple pterygium syndrome", "MULTIPLE PTERYGIUM SYNDROME", "familial pterygium syndrome", "Familial Pterygium Syndrome", "pterygium multiple syndrome", "Escobar syndrome (disorder)", "multiple pterygium syndrome", "Pterygium syndrome, multiple", "Multiple pterygium syndrome (disorder)", "Multiple pterygium syndrome (diagnosis)", "Multiple Pterygium Syndrome, Nonlethal Type", "Escobar variant multiple pterygium syndrome", "MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE", "Multiple Pterygium Syndrome, Escobar Variant", "MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT", "Autosomal recessive multiple pterygium syndrome", "Autosomal recessive non-lethal multiple pterygium syndrome", "contractures, pterygia, and spondylocarpotarsal fusion syndrome", "congenital malformations musculoskeletal system multiple pterygium syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple pterygium syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0012262", "names": ["CFEOM3C", "Feom4 locus", "FEOM4 LOCUS", "FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3C", "fibrosis of extraocular muscles, congenital, 3C", "fibrosis of extraocular muscles, congenital, 3c", "Fibrosis of Extraocular Muscles, Congenital, 3C", "congenital fibrosis of the extraocular muscles 3C"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibrosis of extraocular muscles, congenital, 3c", "shortest_name_length": 7}
{"curie": "MONDO:0014672", "names": ["OI17", "SPARC osteogenesis imperfecta", "osteogenesis imperfecta type 17", "osteogenesis imperfecta, type 17", "osteogenesis imperfecta type XVII", "OSTEOGENESIS IMPERFECTA, TYPE XVII", "osteogenesis imperfecta, type XVII", "osteogenesis imperfecta caused by mutation in SPARC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteogenesis imperfecta type 17", "shortest_name_length": 4}
{"curie": "UMLS:C0013949", "names": ["Embryopathy", "embryopathy", "Embryopathies", "embryopathies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Embryopathies", "shortest_name_length": 11}
{"curie": "MONDO:0006952", "names": ["RLF", "rlf", "ROP", "Terry syndrome", "Terry Syndrome", "Terry's syndrome", "premature retinopathy", "retinopathy premature", "prematurity retinopathy", "retinopathy prematurity", "retrolental fibroplasia", "RETROLENTAL FIBROPLASIA", "Retrolental Fibroplasia", "Retrolental fibroplasia", "fibroplasia retrolental", "Prematurity Retinopathy", "Fibroplasia, Retrolental", "fibroplasia; retrolental", "Retrolental Fibroplasias", "retinopathy; prematurity", "prematurity; retinopathy", "Prematurity Retinopathies", "Fibroplasias, Retrolental", "Retinopathy of Prematurity", "RETINOPATHY OF PREMATURITY", "prematurity of retinopathy", "Retinopathy of prematurity", "retinopathy of prematurity", "prematurity retinopathy rop", "RLF - Retrolental fibroplasia", "Retinopathy of prematurity NOS", "ROP - Retinopathy of prematurity", "retrolental fibroplasia (diagnosis)", "Retinopathy of prematurity (disorder)", "retinopathy of prematurity (diagnosis)", "Retinopathy of prematurity, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinopathy of prematurity", "shortest_name_length": 3}
{"curie": "UMLS:C4526673", "names": ["Unresectable Head and Neck Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Head and Neck Squamous Cell Carcinoma", "shortest_name_length": 50}
{"curie": "UMLS:C2349423", "names": ["medication overuse headache", "Medication overuse headache", "Medication overuse headache (finding)", "medication overuse headache (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Medication overuse headache", "shortest_name_length": 27}
{"curie": "MONDO:0005526", "names": ["TETANUS", "tetanus", "Tetanus", "lockjaw", "Tetanus NOS", "Tetanus (disorder)", "tetanus (diagnosis)", "clostridial tetanus", "Clostridium tetani Infection", "Clostridium tetani infection", "Infection, Clostridium tetani", "Clostridium tetani Infections", "Infections, Clostridium tetani", "Infection due to Clostridium tetani", "infection due to Clostridium tetani", "Infection caused by Clostridium tetani", "Infection caused by Clostridium tetani (disorder)", "Clostridium tetani infectious disease of the nervous system", "Clostridium tetani caused infectious disease of the nervous system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tetanus", "shortest_name_length": 7}
{"curie": "UMLS:C1335104", "names": ["Old Burn Scar-Related Skin Melanoma", "Old Burn Scar-Related Melanoma of Skin", "Old Burn Scar-Related Cutaneous Melanoma", "Old Burn Scar-Related Melanoma of the Skin", "Old Burn Scar-Related Cutaneous (Skin) Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Old Burn Scar-Related Cutaneous Melanoma", "shortest_name_length": 35}
{"curie": "UMLS:C5419026", "names": ["Refractory Extraskeletal Myxoid Chondrosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Extraskeletal Myxoid Chondrosarcoma", "shortest_name_length": 46}
{"curie": "UMLS:C3641182", "names": ["AIDS-Related HPV Infection", "AIDS-related HPV infections", "AIDS-Related Human Papillomavirus Infection", "AIDS-Related Human Papilloma Virus Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Human Papillomavirus Infection", "shortest_name_length": 26}
{"curie": "MONDO:0100484", "names": ["exudative vitreoretinopathy 5", "TSPAN12-related vitreoretinopathy", "TSPAN12 exudative vitreoretinopathy", "exudative vitreoretinopathy caused by mutation in TSPAN12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "TSPAN12-related vitreoretinopathy", "shortest_name_length": 29}
{"curie": "MONDO:0044903", "names": ["Myelofibrosis", "myelofibrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myelofibrosis", "shortest_name_length": 13}
{"curie": "UMLS:C4330524", "names": ["Kir6.2-Associated Diabetes Mellitus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kir6.2-Associated Diabetes Mellitus", "shortest_name_length": 35}
{"curie": "MONDO:0020310", "names": ["FFEVF", "Epilepsy, Partial, with Variable Foci", "familial focal epilepsy with variable foci", "epilepsy, familial focal, with variable foci", "familial partial epilepsy with variable foci"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial focal epilepsy with variable foci", "shortest_name_length": 5}
{"curie": "MONDO:0022792", "names": ["coccydynia", "coccygodynia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "coccygodynia", "shortest_name_length": 10}
{"curie": "UMLS:C4521649", "names": ["IB", "Stage IB Esophageal Adenocarcinoma", "Pathologic Stage IB Esophageal Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IB Esophageal Adenocarcinoma AJCC v8", "shortest_name_length": 2}
{"curie": "MONDO:0017304", "names": ["XLOA", "ocular albinism", "albinism ocular", "Ocular albinism", "Ocular Albinism", "ocular; albinism", "albinism; ocular", "Albinism, Ocular", "Albinism, ocular", "ocular albinism 1", "Albinism ocular 1", "Ocular albinism, NOS", "OA - Ocular albinism", "ocular albinism (disease)", "Ocular albinism (disorder)", "ocular albinism (diagnosis)", "Ocular albinism, unspecified", "Absent pigmentation in the eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ocular albinism", "shortest_name_length": 4}
{"curie": "MONDO:0011174", "names": ["hyperzincemia with functional zinc depletion", "HYPERZINCEMIA WITH FUNCTIONAL ZINC DEPLETION", "Hyperzincemia with Functional Zinc Depletion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperzincemia with functional zinc depletion", "shortest_name_length": 44}
{"curie": "OMIM:611724", "names": ["SHEP8", "Shep8", "SKIN/HAIR/EYE PIGMENTATION 8, FAIR SKIN", "Skin-Hair-Eye Pigmentation 8, Freckling", "SKIN/HAIR/EYE PIGMENTATION 8, BROWN HAIR", "SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 8", "Skin-Hair-Eye Pigmentation, Variation In, 8", "SKIN/HAIR/EYE PIGMENTATION 8, FRECKLING/SUNBURN", "SKIN/HAIR/EYE PIGMENTATION 8, BLUE/LIGHT EYE COLOR"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 5}
{"curie": "MONDO:0032925", "names": ["JRRP", "respiratory papillomatosis, juvenile recurrent, congenital", "RESPIRATORY PAPILLOMATOSIS, JUVENILE RECURRENT, CONGENITAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "respiratory papillomatosis, juvenile recurrent, congenital", "shortest_name_length": 4}
{"curie": "UMLS:C1336087", "names": ["Stage 0 AIDS-Related Anal Canal Cancer", "Stage 0 AIDS-Related Anal Canal Cancer AJCC v6", "Stage 0 AIDS-Related Anal Canal Cancer AJCC v7", "Stage 0 AIDS-Related Anal Carcinoma AJCC v6 and v7", "Stage 0 AIDS-Related Anal Canal Cancer AJCC v6 and v7", "Stage 0 AIDS-Related Anal Canal Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 AIDS-Related Anal Canal Cancer AJCC v6 and v7", "shortest_name_length": 38}
{"curie": "UMLS:C4743673", "names": ["Digestive System Small Cell Carcinoma", "Digestive System Small Cell Neuroendocrine Carcinoma", "Gastrointestinal System Small Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Digestive System Small Cell Neuroendocrine Carcinoma", "shortest_name_length": 37}
{"curie": "UMLS:C0266241", "names": ["bile duct; absent", "bile duct; agenesis", "Agenesis of bile duct", "Congenital absence of bile duct", "Congenital absence of bile ducts", "Agenesis of bile duct (disorder)", "Bile ducts absence of (congenital)", "BILE DUCTS ABSENCE OF (CONGENITAL)", "Congenital absence of bile duct or passage", "Congenital absence of bile duct (disorder)", "Congenital absence of common bile duct or passage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital absence of bile duct", "shortest_name_length": 17}
{"curie": "UMLS:C2721649", "names": ["subgaleal hematoma", "Subgaleal hematoma", "Subgaleal Hematoma", "Subgaleal haematoma", "subgaleal hematoma (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subgaleal haematoma", "shortest_name_length": 18}
{"curie": "OMIM:612874", "names": ["Erythrocyte AMP deaminase deficiency", "Erythrocyte Amp Deaminase Deficiency", "ERYTHROCYTE AMP DEAMINASE DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 36}
{"curie": "UMLS:C0235723", "names": ["FEBRILE REACTION", "Febrile reaction", "reaction febrile", "Reaction febrile", "REACTION FEBRILE", "febrile reactions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Febrile reaction", "shortest_name_length": 16}
{"curie": "UMLS:C2981413", "names": ["Stage IIIB Gastric Gastrointestinal Stromal Tumor", "Stage IIIB Gastric Gastrointestinal Stromal Tumor AJCC v7", "Stage IIIB Gastric (Stomach) Gastrointestinal Stromal Tumor (GIST)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Gastric Gastrointestinal Stromal Tumor", "shortest_name_length": 49}
{"curie": "MONDO:0044332", "names": ["childhood-onset benign chorea with striatal involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood-onset benign chorea with striatal involvement", "shortest_name_length": 55}
{"curie": "MONDO:0005434", "names": ["skin sensitivity to sun"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin sensitivity to sun", "shortest_name_length": 23}
{"curie": "MONDO:0013292", "names": ["Del(4)(q21)", "Monosomy 4q21", "monosomy 4q21", "4q21 microdeletion syndrome", "CHROMOSOME 4q21 DELETION SYNDROME", "chromosome 4q21 deletion syndrome", "4q21 microdeletion syndrome (disorder)", "chromosome 4q21 deletion syndrome, isolated cases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 4q21 deletion syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0020738", "names": ["CSCSC1", "CIRCUMFERENTIAL SKIN CREASES, KUNZE TYPE", "congenital symmetric circumferential skin creases 1", "skin creases, congenital symmetric circumferential, 1", "symmetric circumferential skin creases, congenital, 1", "SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1", "multiple benign circumferential skin creases on limbs 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple benign circumferential skin creases on limbs 1", "shortest_name_length": 6}
{"curie": "MONDO:0007150", "names": ["Gerontoxon", "gerontoxon", "cornea arcus", "arcus cornea", "arcus senilis", "CORNEAL ARCUS", "Arcus corneae", "ARCUS SENILIS", "Arcus senilis", "Corneal arcus", "Corneal Arcus", "corneal arcus", "ARCUS CORNEAE", "arcus corneal", "arcus corneae", "Arcus Senilis", "Arcus Corneae", "Arcus, Corneal", "Arcus lipoidis", "Corneal annulus", "Arcus juvenilis", "arcus of cornea", "Arcus of cornea", "circulus senilis", "Anterior embryotoxon", "Arcus senilis (disorder)", "arcus senilis (diagnosis)", "arcus senilis was observed", "Arcus of cornea (disorder)", "Arcus juvenilis (disorder)", "arcus senilis (physical finding)", "corneal degeneration arcus senilis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arcus senilis", "shortest_name_length": 10}
{"curie": "UMLS:C0275793", "names": ["tonsillitis staphylococcal", "Staphylococcal tonsillitis", "staphylococcal; tonsillitis", "Tonsillitis, staphylococcal", "tonsillitis; staphylococcal", "Staphylococcal tonsillitis (disorder)", "Staphylococcal tonsillitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Staphylococcal tonsillitis", "shortest_name_length": 26}
{"curie": "UMLS:C0281957", "names": ["Radiation Cerebritis", "Radiation-Induced Cerebritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radiation-Induced Cerebritis", "shortest_name_length": 20}
{"curie": "UMLS:C0677714", "names": ["Mantle cell lymphoma stage III", "stage III mantle cell lymphoma", "mantle cell lymphoma stage III", "Mantle Cell Lymphoma Stage III", "Stage III Mantle Cell Lymphoma", "Ann Arbor Stage III Mantle Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mantle cell lymphoma stage III", "shortest_name_length": 30}
{"curie": "MONDO:0005062", "names": ["MLYM", "LYMPHOMA", "Lymphoma", "lymphoma", "Lymphomas", "lymphomas", "Lymphoma NOS", "lymphomatous", "Lymphomatous", "Lymphosarcoma", "Lymphoma, NOS", "Lymphoid Tumor", "germinoblastoma", "lymphoid cancer", "Germinoblastoma", "Germinoblastomas", "Lymphocytic Tumor", "Lymphoid Neoplasm", "LYMPHOMA MALIGNANT", "Malignant lymphoma", "malignant lymphoma", "Malignant Lymphoma", "lymphoma malignant", "Lymphoma malignant", "Lymphoma morphology", "LYMPHOMA, MALIGNANT", "lymphoma, malignant", "Malignant Lymphomas", "malignant lymphomas", "Lymphoma, Malignant", "lymphomas malignant", "Lymphocytic Neoplasm", "Lymphomas, Malignant", "reticulolymphosarcoma", "Reticulolymphosarcoma", "Malignant lymphoma NOS", "Germinoblastic sarcoma", "Reticulolymphosarcomas", "Germinoblastic Sarcoma", "Sarcoma, Germinoblastic", "Malignant lymphoma, NOS", "Germinoblastic Sarcomas", "Sarcomas, Germinoblastic", "Cancer of lymphatic system", "Mixed cell type lymphosarcoma", "Diffuse reticulolymphosarcoma", "lymphosarcoma mixed cell type", "Malignant lymphoma (disorder)", "mixed cell type lymphosarcoma", "malignant lymphoma (diagnosis)", "Lymphoid and Plasmacytic Tumor", "Lymphoid and Plasma Cell Tumor", "Lymphosarcoma, mixed cell type", "Reticulolymphosarcoma, diffuse", "Lymphoid and Plasmacytic Tumour", "Lymphoid and Plasma Cell Tumour", "Lymphoid and Plasmacytic Neoplasm", "Lymphocytic and Plasma Cell Tumor", "lymphoma (Hodgkin and non-Hodgkin)", "Lymphoma (Hodgkin and Non-Hodgkin)", "Lymphocytic and Plasma Cell Tumour", "Malignant lymphoma, mixed cell type", "Lymphocytic and Plasmacytic Neoplasm", "Lymphocytic and Plasma Cell Neoplasm", "lymphoma (Hodgkin's and non-Hodgkin's)", "Lymphoma (Hodgkin's and Non-Hodgkin's)", "mixed cell type lymphosarcoma (diagnosis)", "Malignant lymphoma (morphologic abnormality)", "Malignant lymphoma - mixed small and large cell", "Mixed lymphocytic-histiocytic malignant lymphoma", "Malignant lymphoma, mixed lymphocytic-histiocytic", "Malignant lymphoma - mixed lymphocytic-histiocytic", "Malignant lymphoma, mixed small cell and large cell", "Malignant lymphoma - mixed small and large cell (disorder)", "Mixed small and large cell (diffuse) non-Hodgkin's lymphoma", "Diffuse non-Hodgkin's mixed small and large cell (diffuse) lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphoma", "shortest_name_length": 4}
{"curie": "UMLS:C5555106", "names": ["Yolk Sac Tumor with Somatic-Type Malignancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Yolk Sac Tumor with Somatic-Type Malignancy", "shortest_name_length": 43}
{"curie": "UMLS:C0280451", "names": ["de novo myelodysplastic syndrome", "de novo Myelodysplastic Syndrome", "de myelodysplastic novo syndromes", "de novo myelodysplastic syndromes", "myelodysplastic syndromes, de novo", "Untreated Myelodysplastic Syndrome", "untreated myelodysplastic syndrome", "untreated myelodysplastic syndromes", "myelodysplastic syndromes, untreated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "de novo Myelodysplastic Syndrome", "shortest_name_length": 32}
{"curie": "MONDO:0021458", "names": ["Benign penile tumor", "Benign Penile Tumor", "benign penile tumor", "Benign penile tumour", "Benign tumor of penis", "Benign Tumor of Penis", "benign tumor of penis", "penis benign neoplasm", "benign penile neoplasm", "Benign penile neoplasm", "Benign tumour of penis", "Benign Penile Neoplasm", "Benign Neoplasm of Penis", "benign neoplasm of penis", "Benign neoplasm of penis", "benign tumor of the penis", "BENIGN TUMOR OF THE PENIS", "Benign Tumor of the Penis", "Benign Neoplasm of the Penis", "benign neoplasm of the penis", "Benign neoplasm of penis, NOS", "Benign neoplasm of penis (disorder)", "benign neoplasm of penis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of penis", "shortest_name_length": 19}
{"curie": "UMLS:C3640028", "names": ["Congenital Unilateral Cataract", "Cataract, Congenital, Unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Unilateral Cataract", "shortest_name_length": 30}
{"curie": "UMLS:C1333945", "names": ["Head and neck precancerous condition", "Head and Neck Precancerous Condition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Head and Neck Precancerous Condition", "shortest_name_length": 36}
{"curie": "MONDO:0012497", "names": ["CSNBAD3", "Nougaret type congenital stationary night blindness", "Night Blindness, Congenital Stationary, Nougaret Type", "NIGHT BLINDNESS, CONGENITAL STATIONARY, NOUGARET TYPE", "night blindness, congenital stationary, Nougaret type", "congenital stationary night blindness autosomal dominant 3", "Night Blindness, Congenital Stationary, Autosomal Dominant 3", "NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 3", "night blindness, congenital stationary, autosomal dominant 3", "congenital stationary night blindness autosomal dominant type 3", "night blindness, congenital stationary, autosomal dominant type 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital stationary night blindness autosomal dominant 3", "shortest_name_length": 7}
{"curie": "MONDO:0009936", "names": ["lung agenesis", "LUNG AGENESIS", "Primary pulmonary hypoplasia", "primary pulmonary hypoplasia", "pulmonary hypoplasia, primary", "Pulmonary Hypoplasia, Primary", "PULMONARY HYPOPLASIA, PRIMARY", "Idiopathic pulmonary hypoplasia", "familial primary pulmonary hypoplasia", "Primary pulmonary hypoplasia (disorder)", "primary pulmonary hypoplasia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial primary pulmonary hypoplasia", "shortest_name_length": 13}
{"curie": "UMLS:C1335033", "names": ["Non-Neoplastic Pituitary Gland Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Pituitary Gland Disorder", "shortest_name_length": 39}
{"curie": "UMLS:C3900027", "names": ["Anti-D Hemolytic Disease of the Newborn", "Isoimmunization of Newborn with Rhesus Anti-D Antibody"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anti-D Hemolytic Disease of the Newborn", "shortest_name_length": 39}
{"curie": "UMLS:C0404867", "names": ["pregnancy angular", "Angular pregnancy", "Angular Pregnancy", "Pregnancy, Angular", "Angular Pregnancies", "Pregnancies, Angular", "Angular pregnancy (disorder)", "Angular pregnancy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pregnancy, Angular", "shortest_name_length": 17}
{"curie": "MONDO:0012482", "names": ["WNV, SUSCEPTIBILITY TO", "WNV, susceptibility to", "WEST NILE VIRUS, SUSCEPTIBILITY TO", "West Nile virus, susceptibility to", "WEST NILE VIRUS, SUSCEPTIBILITY TO (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "West Nile virus, susceptibility to", "shortest_name_length": 22}
{"curie": "MONDO:0002834", "names": ["prostate urothelial carcinoma", "Prostate Urothelial Carcinoma", "primary prostate urothelial cancer", "Primary Prostate Urothelial Cancer", "prostate transitional cell carcinoma", "Prostate Transitional Cell Carcinoma", "Primary Prostate Urothelial Carcinoma", "primary prostate urothelial carcinoma", "transitional cell carcinoma of prostate", "Transitional Cell Carcinoma of Prostate", "prostate gland transitional cell carcinoma", "Transitional Cell Carcinoma of the Prostate", "transitional cell carcinoma of the prostate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary prostate urothelial carcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0009044", "names": ["HBLRCN1", "UGT deficiency", "Crigler-Najjar type 1", "crigler-najjar disease", "Crigler-Najar Syndrome", "Crigler Najar Syndrome", "CRIGLER-NAJJAR DISEASE", "CRIGLER-NAJJAR SYNDROME", "Crigler-Najjar syndrome", "Crigler Najjar Syndrome", "crigler najjar syndrome", "crigler-najjar syndrome", "Crigler-Najjar Syndrome", "Crigler Najjar syndrome", "crigler najjar syndromes", "Bilirubin-UGT deficiency", "Crigler Najjar Syndromes", "Najjar Syndrome, Crigler", "Syndrome, Crigler Najjar", "bilirubin-UGT deficiency", "Crigler-Najjar syndrome, NOS", "type I Crigler Najjar syndrome", "Crigler-Najjar syndrome type 1", "Crigler-Najjar syndrome type I", "Crigler-Najjar Syndrome, Type I", "Crigler Najjar Syndrome, Type I", "Crigler-Najjar syndrome, type I", "Crigler Najjar syndrome, type 1", "CRIGLER-NAJJAR SYNDROME, TYPE I", "Crigler Najjar Syndrome, Type 1", "Bilirubin-UGT deficiency type 1", "Glucuronyltransferase deficiency", "glucuronyl transferase deficiency", "crigler-Najjar disease or syndrome", "deficiency; glucuronyl transferase", "glucuronyl transferase; deficiency", "Crigler-Najjar syndrome (disorder)", "UDP glucuronyl transferase deficiency", "Deficiency of glucuronosyltransferase", "glucuronyl transferase deficiency type I", "HYPERBILIRUBINEMIA, CRIGLER-NAJJAR TYPE I", "Crigler-Najjar syndrome, type I (disorder)", "hereditary unconjugated hyperbilirubinemia", "Hereditary Unconjugated Hyperbilirubinemia", "Hyperbilirubinemia, Hereditary Unconjugated", "Unconjugated Hyperbilirubinemia, Hereditary", "Hereditary Unconjugated Hyperbilirubinemias", "Bilirubin glucuronosyltransferase deficiency", "glucuronyl transferase deficiency (diagnosis)", "kernicterus; crigler-Najjar disease or syndrome", "bilirubin UDP glucuronyl transferase deficiency", "Bilirubin UDP glucuronyl transferase deficiency", "jaundice; crigler-Najjar disease or syndrome (fetus)", "Familial Nonhemolytic Unconjugated Hyperbilirubinemia", "glucuronyl transferase deficiency type I (Crigler-Najjar I)", "bilirubin uridinediphosphate glucuronosyltransferase deficiency", "Bilirubin uridinediphosphate glucuronosyltransferase deficiency", "Bilirubin uridinediphosphate glucuronosyltransferase deficiency type 1", "glucuronyl transferase deficiency type I (Crigler-Najjar I) (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Crigler-Najjar syndrome", "shortest_name_length": 7}
{"curie": "MONDO:0017496", "names": ["Femorotibiofibular intercalary transverse meromelia, unilateral", "congenital absence of thigh and lower leg with foot present, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital absence of thigh and lower leg with foot present, unilateral", "shortest_name_length": 63}
{"curie": "UMLS:C4552018", "names": ["Stage IIIC", "Stage IIIC Cancer of Testis", "stage IIIC cancer of testis", "Stage IIIC Testicular Cancer", "stage IIIC testicular cancer", "stage IIIC cancer of the testis", "Stage IIIC Cancer of the Testis", "stage IIIC testicular cancer AJCC v7", "Stage IIIC Testicular Cancer AJCC v7", "Stage IIIC Testicular Cancer AJCC v6", "stage IIIC testicular cancer AJCC v6", "Stage IIIC Testicular Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIC Testicular Cancer AJCC v6 and v7", "shortest_name_length": 10}
{"curie": "UMLS:C1333418", "names": ["Epipodophyllotoxin Related Myelodysplastic Syndrome", "Epipodophyllotoxin-Related Myelodysplastic Syndrome", "Therapy-related myelodysplastic syndrome, epipodophyllotoxin-related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epipodophyllotoxin-Related Myelodysplastic Syndrome", "shortest_name_length": 51}
{"curie": "MONDO:0017501", "names": ["tibiofibular terminal transverse meromelia, bilateral", "congenital absence of both lower leg and foot, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital absence of both lower leg and foot, bilateral", "shortest_name_length": 53}
{"curie": "MONDO:0020811", "names": ["mitochondrial complex III deficiency, nuclear type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex III deficiency, nuclear type", "shortest_name_length": 50}
{"curie": "MONDO:0030270", "names": ["LMPHM9", "LYMPHATIC MALFORMATION 9", "lymphatic malformation 9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphatic malformation 9", "shortest_name_length": 6}
{"curie": "UMLS:C5555025", "names": ["NTRK-Rearranged Mesenchymal Tumor", "Lipofibromatosis-Like Neural Tumor", "NTRK-Rearranged Spindle Cell Neoplasm", "NTRK-Positive Tumor Resembling Peripheral Nerve Sheath Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "NTRK-Rearranged Spindle Cell Neoplasm", "shortest_name_length": 33}
{"curie": "MONDO:0010706", "names": ["Pof1", "POF1", "POFX", "ovarian failure, premature", "PREMATURE OVARIAN FAILURE 1", "Premature Ovarian Failure 1", "premature ovarian failure 1", "FMR1 primary ovarian failure", "primary ovarian insufficiency 1", "premature ovarian failure type 1", "familial premature ovarian failure", "PREMATURE OVARIAN FAILURE, X-LINKED", "Premature Ovarian Failure, X Linked", "premature ovarian failure, X-linked", "Fragile X Premature Ovarian Failure", "Premature Ovarian Failure, X-Linked", "FRAGILE X PREMATURE OVARIAN FAILURE", "FMR1-related premature ovarian failure", "X-Linked Hypergonadotropic Ovarian Failure", "X Linked Hypergonadotropic Ovarian Failure", "FMR1-related primary ovarian insufficiency", "FMR1-Related Primary Ovarian Insufficiency", "FMR1 Related Primary Ovarian Insufficiency", "Hypergonadotropic Ovarian Failure, X Linked", "hypergonadotropic ovarian failure, X-linked", "HYPERGONADOTROPIC OVARIAN FAILURE, X-LINKED", "Hypergonadotropic Ovarian Failure, X-Linked", "idiopathic familial premature ovarian failure", "Fragile X-associated primary ovarian insufficiency", "Fragile X-Associated Primary Ovarian Insufficiency", "Fragile X Associated Primary Ovarian Insufficiency", "primary ovarian failure caused by mutation in FMR1", "fragile X-associated primary ovarian insufficiency", "Primary Ovarian Insufficiency, Fragile X-Associated", "PRIMARY OVARIAN INSUFFICIENCY, FRAGILE X-ASSOCIATED", "Primary Ovarian Insufficiency, Fragile X Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "premature ovarian failure 1", "shortest_name_length": 4}
{"curie": "MONDO:0014837", "names": ["THC6", "THROMBOCYTOPENIA 6", "thrombocytopenia 6", "thrombocytopenia type 6", "THROMBOCYTOPENIA, AUTOSOMAL DOMINANT, 6", "thrombocytopenia, autosomal dominant, 6", "hereditary thrombocytopenia with early-onset myelofibrosis", "Hereditary thrombocytopenia with early-onset myelofibrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombocytopenia 6", "shortest_name_length": 4}
{"curie": "MONDO:0019271", "names": ["acrokeratoderma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acrokeratoderma", "shortest_name_length": 15}
{"curie": "MONDO:0030332", "names": ["CILD46", "ciliary dyskinesia, primary, 46", "CILIARY DYSKINESIA, PRIMARY, 46"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ciliary dyskinesia, primary, 46", "shortest_name_length": 6}
{"curie": "MONDO:0032818", "names": ["NEDCHS", "NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR HYPOPLASIA AND SPASTICITY", "neurodevelopmental disorder with cerebellar hypoplasia and spasticity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with cerebellar hypoplasia and spasticity", "shortest_name_length": 6}
{"curie": "UMLS:C5419205", "names": ["Refractory Esophageal Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Esophageal Squamous Cell Carcinoma", "shortest_name_length": 45}
{"curie": "MONDO:0018304", "names": ["Schnitzler syndrome", "Schnitzler Syndrome", "Schnitzler's syndrome", "Schnitzler syndrome (disorder)", "Chronic urticaria with gammopathy", "chronic urticaria with gammopathy", "chronic urticaria with gammapathy", "Chronic urticaria with macroglobulinemia", "chronic urticaria with macroglobulinemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Schnitzler syndrome", "shortest_name_length": 19}
{"curie": "MONDO:0011906", "names": ["CBAS1", "BASD1", "congenital bile acid synthesis defect 1", "bile acid synthesis defect, congenital, 1", "BILE ACID SYNTHESIS DEFECT, CONGENITAL, 1", "Bile acid synthesis defect, congenital, 1", "congenital bile acid synthesis defect type 1", "Congenital bile acid synthesis defect type 1", "HSD3B7 congenital bile acid synthesis defect", "congenital bile acid synthesis defect, type 1", "bile acid synthesis defect, congenital, type 1", "Congenital Bile Acid Synthesis Defect Type 1 (CBAS1)", "3-Beta-hydroxy-delta-5-C27-steroid dehydrogenase deficiency", "3-beta-hydroxy-delta-5-C27-steroid oxidoreductase deficiency", "3-BETA-HYDROXY-DELTA-5-C27-STEROID OXIDOREDUCTASE DEFICIENCY", "3-Beta-hydroxy-Delta-5-C27-steroid oxidoreductase deficiency", "3-Beta-Hydroxy-Delta-5-C27-Steroid Oxidoreductase, Deficiency Of", "congenital bile acid synthesis defect caused by mutation in HSD3B7", "3-beta-hydroxy-delta-5-C27-steroid oxidoreductase deficiency type 1", "3-alpha beta-hydroxy-delta-5-C27-steroid oxidoreductase, deficiency of", "3-Beta-hydroxy-delta-5-C27-steroid dehydrogenase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital bile acid synthesis defect 1", "shortest_name_length": 5}
{"curie": "MONDO:0004633", "names": ["MCHL", "MCCHL", "Hodgkin; mixed cellularity", "Mixed cellularity Hodgkin lymphoma", "Mixed Cellularity Hodgkin Lymphoma", "Hodgkin disease, mixed cellularity", "Hodgkin mixed cellularity lymphoma", "mixed cellularity Hodgkin lymphoma", "mixed cellularity Hodgkin's disease", "Hodgkin's disease mixed cellularity", "Mixed Cellularity Hodgkin's Disease", "Hodgkin lymphoma, mixed cellularity", "Hodgkin's Disease Mixed Cellularity", "Hodgkin's lymphoma mixed cellularity", "Hodgkins lymphoma, mixed cellularity", "Hodgkin's Lymphoma Mixed Cellularity", "Mixed Cellularity Hodgkin's Lymphoma", "Hodgkin's disease, mixed cellularity", "mixed cellularity Hodgkin's lymphoma", "Hodgkin's lymphoma, mixed cellularity", "disease; Hodgkin's, mixed cellularity", "[M]Hodgkin's disease, mixed cellularity", "Hodgkin's disease, mixed cellularity NOS", "Hodgkin Lymphoma, Mixed Cellularity, NOS", "Hodgkin's disease with mixed cellularity", "Hodgkin's disease, mixed cellularity, NOS", "Mixed cellularity Classic Hodgkin lymphoma", "Mixed Cellularity Classic Hodgkin Lymphoma", "Mixed Cellularity Classical Hodgkin Lymphoma", "mixed cellularity classical Hodgkin lymphoma", "Mixed cellularity classical Hodgkin lymphoma", "Classical Hodgkin lymphoma, mixed cellularity", "mixed cellularity Hodgkin lymphoma (diagnosis)", "Hodgkin's disease, mixed cellularity (clinical)", "Hodgkin's disease, mixed cellularity (disorder)", "Classic Hodgkin lymphoma, mixed cellularity type", "classic Hodgkin lymphoma, mixed cellularity type", "Hodgkin's disease mixed cellularity stage unspecified", "Hodgkin's disease, mixed cellularity of unspecified site", "Hodgkin lymphoma, mixed cellularity (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's lymphoma, mixed cellularity", "shortest_name_length": 4}
{"curie": "MONDO:0005536", "names": ["pancolitis", "universal colitis", "pan-ulcerative colitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancolitis", "shortest_name_length": 10}
{"curie": "UMLS:C0235667", "names": ["MASTITIS ACUTE FEMALE", "Mastitis acute female"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mastitis acute female", "shortest_name_length": 21}
{"curie": "UMLS:C3837219", "names": ["Hoarding disorder", "hoarding disorder", "Hoarding Disorder", "Hoarding Disorders", "Disorders, Hoarding", "hoarding disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hoarding Disorder", "shortest_name_length": 17}
{"curie": "MONDO:0003653", "names": ["stork bite", "Unna's nevus", "Salmon patch nevus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stork bite", "shortest_name_length": 10}
{"curie": "UMLS:C0338468", "names": ["Vocal Tic Disorder", "Vocal tic disorder", "vocal tic disorder", "Vocal Tic Disorders", "Tic Disorder, Vocal", "Tic Disorders, Vocal", "Vocal tic disorder (disorder)", "vocal tic disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tic Disorders, Vocal", "shortest_name_length": 18}
{"curie": "MONDO:0022839", "names": ["neonatal HIV", "congenital HIV", "HIV infection congenital", "Congenital HIV infection", "Congenital HIV infection (diagnosis)", "neonatal human immunodeficiency virus", "congenital human immunodeficiency virus", "Congenital human immunodeficiency virus infection", "Congenital human immunodeficiency virus infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital human immunodeficiency virus", "shortest_name_length": 12}
{"curie": "UMLS:C1275661", "names": ["AML with recurrent genetic abnormality", "AML with Recurrent Genetic Abnormalities", "Acute myeloid leukemia with recurrent genetic abnormality", "Acute myeloid leukaemia with recurrent genetic abnormality", "Acute Myeloid Leukemia with Recurrent Genetic Abnormalities", "Acute Myeloid Leukemia with Balanced Translocations/Inversions", "Acute myeloid leukemia with recurrent genetic abnormality (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute myeloid leukemia with recurrent genetic abnormality", "shortest_name_length": 38}
{"curie": "UMLS:C2363980", "names": ["Cross resistance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cross resistance", "shortest_name_length": 16}
{"curie": "MONDO:0020398", "names": ["Duroziez", "Duroziez's disease", "congenital mitral stenosis", "Congenital mitral stenosis", "Stenosis;mitral;congenital", "mitral stenosis congenital", "stenosis; mitral, congenital", "mitral; stenosis, congenital", "MS - Congenital mitral stenosis", "Congenital mitral valve stenosis", "hereditary mitral valve stenosis", "congenital mitral valve stenosis", "Congenital stenosis of mitral valve", "congenital mitral stenosis (disease)", "congenital mitral valve stenosis (diagnosis)", "Congenital stenosis of mitral valve (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital mitral stenosis", "shortest_name_length": 8}
{"curie": "UMLS:C1332910", "names": ["Ceruminous Tumor", "Ceruminous Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ceruminous Neoplasm", "shortest_name_length": 16}
{"curie": "MONDO:0002659", "names": ["uvea cancer", "Uveal tumor", "uveal tumor", "uveal cancer", "cancer of uvea", "Malignant Uvea Tumor", "malignant uvea tumor", "malignant uveal tumor", "Malignant Uveal Tumor", "malignant Uveal tumor", "Malignant Tumor of Uvea", "malignant tumor of uvea", "malignant uvea neoplasm", "Malignant Uvea Neoplasm", "malignant uveal neoplasm", "Malignant Uveal Neoplasm", "malignant neoplasm of uvea", "Malignant Neoplasm of Uvea", "Malignant Tumor of the Uvea", "malignant tumor of the uvea", "Malignant Neoplasm of the Uvea", "malignant neoplasm of the uvea", "Malignant Uveal Tract Neoplasm", "Malignant neoplasm of uveal tract", "malignant tumor of uveal tract of eye", "malignant neoplasm of uveal tract of eye", "malignant neoplasm of uveal tract of eye (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uveal cancer", "shortest_name_length": 11}
{"curie": "MONDO:0032939", "names": ["MRD63", "Mental Retardation, Autosomal Dominant 63, With Macrocephaly", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 63, WITH MACROCEPHALY", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 63, WITH MACROCEPHALY", "intellectual developmental disorder, autosomal dominant 63, with macrocephaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual developmental disorder, autosomal dominant 63, with macrocephaly", "shortest_name_length": 5}
{"curie": "MONDO:0002130", "names": ["Mononeuritis;arms", "mononeuritis upper limb", "Mononeuritis upper limb", "mononeuritis of the arms", "upper limb; mononeuritis", "mononeuritis; upper limb", "upper limb mononeuronitis", "mononeuritis of upper limb", "UPPER EXTREMITY MONONEURITIS", "mononeuritis of an upper limb", "forelimb mononeuritis simplex", "Mononeuritis of upper limb, NOS", "mononeuritis simplex of forelimb", "mononeuritis of upper limb (diagnosis)", "Mononeuritis of upper limb, unspecified", "mononeuritis of upper limb, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "upper limb mononeuronitis", "shortest_name_length": 17}
{"curie": "UMLS:C0151606", "names": ["LABIAL EDEMA", "Edema labial genital", "EDEMA LABIAL GENITAL", "Oedema labial genital"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Edema labial genital", "shortest_name_length": 12}
{"curie": "UMLS:C1710225", "names": ["Subcutaneous Nodular Fasciitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subcutaneous Nodular Fasciitis", "shortest_name_length": 30}
{"curie": "MONDO:0014887", "names": ["BMFS3", "bone marrow failure syndrome 3", "BONE MARROW FAILURE SYNDROME 3", "bone marrow failure syndrome type 3", "DNAJC21 bone marrow failure syndrome", "bone marrow failure syndrome caused by mutation in DNAJC21"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bone marrow failure syndrome 3", "shortest_name_length": 5}
{"curie": "MONDO:0007266", "names": ["CMH2", "hypertrophic cardiomyopathy 2", "cardiomyopathy, hypertrophic, 2", "TNNT2 hypertrophic cardiomyopathy", "hypertrophic cardiomyopathy type 2", "cardiomyopathy familial hypertrophic 2", "Cardiomyopathy, Familial Hypertrophic, 2", "CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 2", "cardiomyopathy, familial hypertrophic, 2", "familial hypertrophic cardiomyopathy type 2", "Familial Hypertrophic Cardiomyopathy Type 2", "cardiomyopathy, familial hypertrophic, type 2", "hypertrophic cardiomyopathy caused by mutation in TNNT2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophic cardiomyopathy 2", "shortest_name_length": 4}
{"curie": "MONDO:0010057", "names": ["Ryukyuan muscular atrophy", "spinal muscular atrophy Ryukyuan type", "spinal muscular atrophy, Ryukyuan type", "Spinal muscular atrophy, Ryukyuan type", "SPINAL MUSCULAR ATROPHY, RYUKYUAN TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal muscular atrophy, Ryukyuan type", "shortest_name_length": 25}
{"curie": "MONDO:0007540", "names": ["MEN1", "MEN I", "men 1", "MEA I", "MEN 1", "MEA 1", "MEA type I", "MEN Type I", "men type 1", "MEA Type 1", "men type I", "men type i", "MEN type I", "MEA Type I", "MEN Type 1", "MEA type 1", "MEA, type 1", "MEN, type 1", "MEN1 syndrome", "MEN 1 syndrome", "men 1 syndrome", "Wermer Syndrome", "wermer syndrome", "Wermer syndrome", "WERMER SYNDROME", "wermer's syndrome", "Wermer's syndrome", "Wermer's Syndrome", "MEA syndrome, type I", "MEN1 somatic mutations", "MEN1 SOMATIC MUTATIONS", "ADENOMATOSIS, POLYGLANDULAR", "multiple endocrine neoplasia 1", "multiple endocrine adenomatosis", "endocrine adenomatosis multiple", "Multiple Endocrine Adenomatosis", "ENDOCRINE ADENOMATOSIS, MULTIPLE", "endocrine adenomatosis, multiple", "MEN1 multiple endocrine neoplasia", "Multiple Endocrine Neoplasms Type 1", "type I multiple endocrine neoplasia", "Multiple endocrine neoplasia Type 1", "Multiple endocrine neoplasia type 1", "Multiple endocrine neoplasia Type I", "Multiple Endocrine Neoplasia Type I", "Multiple Endocrine Neoplasia Type 1", "MULTIPLE ENDOCRINE NEOPLASIA TYPE I", "MULTIPLE ENDOCRINE NEOPLASIA TYPE 1", "multiple endocrine neoplasia type 1", "multiple endocrine neoplasia type I", "Neoplasms, Multiple Endocrine Type I", "Neoplasms, Multiple Endocrine Type 1", "multiple endocrine neoplasia, type 1", "Multiple Endocrine Neoplasia, Type I", "Multiple endocrine neoplasia, type 1", "Neoplasia, Multiple Endocrine Type 1", "MULTIPLE ENDOCRINE NEOPLASIA, TYPE I", "multiple endocrine neoplasia, type I", "Multiple endocrine adenomatosis Type I", "Multiple Endocrine Adenomatosis Type 1", "multiple endocrine adenomatosis type 1", "multiple endocrine adenomatosis type I", "Multiple Endocrine Adenomatosis Type I", "ENDOCRINE ADENOMA PEPTIC ULCER COMPLEX", "Multiple endocrine adenomatosis, type 1", "multiple endocrine adenomatosis, type I", "Multiple endocrine adenomatosis, type I", "Multiple Endocrine Adenomatosis, Type I", "Multiple endocrine neoplasia [MEN] type I", "multiple endocrine neoplasia type 1 (MEN1)", "Multiple endocrine neoplasia syndrome type 1", "multiple endocrine neoplasia type 1 syndrome", "Multiple endocrine neoplasia, type 1 (disorder)", "multiple endocrine neoplasia, type I (diagnosis)", "MEN 1 - Multiple endocrine neoplasia syndrome type 1", "multiple endocrine neoplasia caused by mutation in MEN1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple endocrine neoplasia type 1", "shortest_name_length": 4}
{"curie": "MONDO:0010587", "names": ["EDVX", "EDV2", "X-linked epidermodysplasia verruciformis", "Epidermodysplasia Verruciformis, X-Linked", "epidermodysplasia verruciformis, X-linked", "EPIDERMODYSPLASIA VERRUCIFORMIS, X-LINKED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermodysplasia verruciformis, X-linked", "shortest_name_length": 4}
{"curie": "UMLS:C0433900", "names": ["Spinal Cord Laceration", "Cord Laceration, Spinal", "Laceration, Spinal Cord", "spinal cord; laceration", "Spinal Cord Lacerations", "laceration; spinal cord", "Lacerations, Spinal Cord", "Cord Lacerations, Spinal", "Laceration of spinal cord", "spinal cord injury laceration", "Laceration of spinal cord (disorder)", "Laceration of spinal cord (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spinal Cord Laceration", "shortest_name_length": 22}
{"curie": "MONDO:0003476", "names": ["Clear cell ependymoma", "clear cell ependymoma", "Clear Cell Ependymoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "clear cell ependymoma", "shortest_name_length": 21}
{"curie": "UMLS:C4526723", "names": ["Stage IIIB", "Stage IIIB Lung Cancer", "Stage IIIB Lung Cancer AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Lung Cancer AJCC v8", "shortest_name_length": 10}
{"curie": "UMLS:C3897738", "names": ["Recurrent Fallopian Tube Cancer", "recurrent fallopian tube cancer", "Recurrent Fallopian Tube Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Fallopian Tube Carcinoma", "shortest_name_length": 31}
{"curie": "UMLS:C4726596", "names": ["Recurrent Double-Hit Lymphoma", "Recurrent High Grade B-Cell Lymphoma with MYC and BCL2 or BCL6 Rearrangements", "Recurrent High-Grade B-Cell Lymphoma with MYC and BCL2 or BCL6 Rearrangements"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent High Grade B-Cell Lymphoma with MYC and BCL2 or BCL6 Rearrangements", "shortest_name_length": 29}
{"curie": "UMLS:C0852967", "names": ["Acne aggravated", "Aggravated Acne", "Exacerbation of acne"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acne aggravated", "shortest_name_length": 15}
{"curie": "MONDO:0000644", "names": ["Benign cervical tumor", "Benign tumor of cervix", "benign tumor of cervix", "Benign cervical tumour", "Cervix neoplasms benign", "Benign tumour of cervix", "benign cervical neoplasm", "cervical benign neoplasm", "Benign Cervical Neoplasm", "benign cervix uteri tumor", "benign neoplasm of cervix", "Benign Cervix Uteri Tumor", "Benign Uterine Cervix Tumor", "benign uterine cervix tumor", "benign tumor of cervix uteri", "Benign Cervix Uteri Neoplasm", "Benign Tumor of Cervix Uteri", "benign cervix uteri neoplasm", "Benign Tumor of Uterine Cervix", "benign tumor of uterine cervix", "benign uterine cervix neoplasm", "uterine cervix benign neoplasm", "Benign Uterine Cervix Neoplasm", "benign neoplasm of cervix uteri", "Benign Neoplasm of Cervix Uteri", "Benign neoplasm of cervix uteri", "Benign Tumor of the Cervix Uteri", "benign tumor of the cervix uteri", "Benign Cervix Uteri Neoplasm NOS", "Benign cervix uteri neoplasm NOS", "benign neoplasm of uterine cervix", "Benign neoplasm of uterine cervix", "Benign Neoplasm of Uterine Cervix", "Benign Tumor of the Uterine Cervix", "benign tumor of the uterine cervix", "benign neoplasm of the cervix uteri", "Benign Neoplasm of the Cervix Uteri", "benign neoplasm of cervix (diagnosis)", "Benign Neoplasm of the Uterine Cervix", "benign neoplasm of the uterine cervix", "Benign neoplasm of uterine cervix (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical benign neoplasm", "shortest_name_length": 21}
{"curie": "MONDO:0020675", "names": ["ISCHEMIA BOWEL", "Ischemia bowel", "Bowel ischemia", "BOWEL ISCHEMIA", "ISCHEMIA INTEST", "Ischaemia bowel", "ischemia; bowel", "Bowel ischaemia", "Intestinal ischemia", "INTESTINAL ISCHEMIA", "Intestinal ischaemia", "INTESTINAL ISCHAEMIA", "ischemic bowel disease", "Ischemic Bowel Disease", "Ischemic bowel disease", "ischemic bowel disorder", "Ischaemic bowel disease", "Ischemic disease of gut", "Ischaemic disease of gut", "Ischemic bowel disease, NOS", "Ischaemic bowel disease, NOS", "vascular intestinal insufficiency", "Vascular insufficiency of intestine", "Vascular insufficiency of the intestine", "Vascular insufficiency of intestine, NOS", "vascular intestinal insufficiency (diagnosis)", "Vascular insufficiency of intestine (disorder)", "Unspecified vascular insufficiency of intestine", "Vascular insufficiency of intestine, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ischemic bowel disorder", "shortest_name_length": 14}
{"curie": "MONDO:0009972", "names": ["RESPIRATORY UNDERRESPONSIVENESS TO HYPOXIA AND HYPERCAPNIA", "Respiratory Underresponsiveness to Hypoxia and Hypercapnia", "respiratory underresponsiveness to hypoxia and hypercapnia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "respiratory underresponsiveness to hypoxia and hypercapnia", "shortest_name_length": 58}
{"curie": "UMLS:C4289792", "names": ["CAEBV", "Chronic Active EBV Infection", "Chronic Active Epstein-Barr Virus", "Systemic CAEBV of T-and NK-Cell Type", "Chronic active Epstein-Barr virus (without identified mutation)", "Systemic Chronic Active EBV Infection of T-Cell and NK-Cell Type", "Chronic Active EBV Infection of T-and NK-Cell Type, Systemic Form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic Active EBV Infection of T-and NK-Cell Type, Systemic Form", "shortest_name_length": 5}
{"curie": "MONDO:0021291", "names": ["Gastric Fundus Carcinoma In Situ", "Cancer in situ fundus of stomach", "Stage 0 Gastric Fundus Carcinoma", "gastric fundus carcinoma in situ", "stage 0 gastric fundus carcinoma", "fundus of stomach carcinoma in situ", "fundus of stomach in situ carcinoma", "carcinoma in situ of gastric fundus", "stage 0 fundus of stomach carcinoma", "Carcinoma in situ of Gastric Fundus", "Carcinoma in situ of fundus of stomach", "carcinoma in situ of fundus of stomach", "Carcinoma in situ of Fundus of Stomach", "Carcinoma in situ of the Gastric Fundus", "carcinoma in situ of the gastric fundus", "Carcinoma in situ of the Fundus of the Stomach", "carcinoma in situ of the fundus of the stomach", "gastric fundus carcinoma in situ aJCC v6 and v7", "Gastric Fundus Carcinoma In Situ AJCC v6 and v7", "Carcinoma in situ of fundus of stomach (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma in situ of fundus of stomach", "shortest_name_length": 32}
{"curie": "MONDO:0007190", "names": ["DBM", "BCLL", "CLLS2", "Clls2", "B-CELL MALIGNANCY, LOW-GRADE", "B-cell malignancy, low-grade", "DISRUPTED IN B-CELL MALIGNANCY", "disrupted in B-cell malignancy", "LEUKEMIA, CHRONIC LYMPHOCYTIC, B-CELL", "leukemia, chronic lymphocytic, B-cell", "leukemia, chronic lymphocytic, susceptibility to, 2", "LEUKEMIA, CHRONIC LYMPHOCYTIC, SUSCEPTIBILITY TO, 2", "leukemia, chronic lymphocytic, susceptibility to, type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukemia, chronic lymphocytic, susceptibility to, 2", "shortest_name_length": 3}
{"curie": "UMLS:C1514802", "names": ["Recurrent High Grade Burkitt-Like Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent High Grade Burkitt-Like Lymphoma", "shortest_name_length": 42}
{"curie": "UMLS:C4524720", "names": ["Clinical Stage IVB Gastroesophageal Junction Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage IVB Gastroesophageal Junction Adenocarcinoma AJCC v8", "shortest_name_length": 67}
{"curie": "MONDO:0011934", "names": ["GCF", "DFSP", "Juvenile DFSP", "Juvenile DFSPs", "DFSP, Juvenile", "DFSPs, Juvenile", "DERMATOFIBROSARCOMA", "Dermatofibrosarcoma", "dermatofibrosarcoma", "Dermatofibrosarcomas", "Darier Ferrand Tumor", "Darier-Ferrand Tumor", "Darier-Hoffmann Tumor", "Darier Hoffmann Tumor", "Tumor, Darier-Ferrand", "Tumor, Darier-Hoffmann", "Dermatofibrosarcoma NOS", "giant cell fibroblastoma", "Giant cell fibroblastoma", "GIANT CELL FIBROBLASTOMA", "Dermatofibrosarcoma, NOS", "Giant Cell Fibroblastoma", "Giant Cell Fibroblastomas", "Fibroblastoma, Giant Cell", "Cell Fibroblastoma, Giant", "Fibroblastomas, Giant Cell", "Dermatofibroma protuberans", "Cell Fibroblastomas, Giant", "Dermatofibrosarcoma Protuberan", "dermatofibrosarcoma protuberans", "Dermatofibrosarcoma Protuberans", "DERMATOFIBROSARCOMA PROTUBERANS", "Dermatofibrosarcoma protuberans", "Protuberan, Dermatofibrosarcoma", "dermatofibrosarcoma; protuberans", "Protuberans, Dermatofibrosarcoma", "protuberans; dermatofibrosarcoma", "Giant cell fibroblastoma of skin", "dermatofibrosarcomas protuberans", "Giant Dermatofibrosarcoma Protuberan", "Dermatofibrosarcoma protuberans, NOS", "Giant Dermatofibrosarcoma Protuberans", "Protuberan, Giant Dermatofibrosarcoma", "Dermatofibrosarcoma Protuberan, Giant", "DFSP - dermatofibrosarcoma protuberans", "skin neoplasm giant cell fibroblastoma", "Protuberans, Giant Dermatofibrosarcoma", "Dermatofibrosarcoma Protuberans, Giant", "DFSP - Dermatofibrosarcoma protruberans", "Familial Dermatofibrosarcoma Protuberan", "Dermatofibrosarcoma Protuberan, Familial", "Protuberan, Familial Dermatofibrosarcoma", "Familial Dermatofibrosarcoma Protuberans", "Dermatofibrosarcoma Protuberans, Familial", "Protuberans, Familial Dermatofibrosarcoma", "Dermatofibrosarcoma protuberans (disorder)", "Giant cell fibroblastoma of skin (disorder)", "Dermatofibrosarcoma Protuberans, Giant Cell", "Dermatofibrosarcoma protuberans (diagnosis)", "Giant cell fibroblastoma of skin (diagnosis)", "Dermatofibrosarcoma (morphologic abnormality)", "familial dermatofibrosarcoma protuberans (subtype)", "Giant cell fibroblastoma (morphologic abnormality)", "metastatic dermatofibrosarcoma protuberans (subtype)", "soft tissue malignant neoplasm dermatofibrosarcoma protuberans"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermatofibrosarcoma protuberans", "shortest_name_length": 3}
{"curie": "MONDO:0008048", "names": ["CNM1", "CNM3", "AD-CNM", "centronuclear myopathy 1", "Centronuclear Myopathy 1", "Myopathy, Centronuclear, 1", "myopathy, centronuclear, 3", "myopathy, centronuclear, 1", "MYOPATHY, CENTRONUCLEAR, 1", "myopathy, centronuclear, type 3", "myopathy, centronuclear, type 1", "DNM2-related centronuclear myopathy", "Myotubular Myopathy, Autosomal Dominant", "MYOTUBULAR MYOPATHY, AUTOSOMAL DOMINANT", "myotubular myopathy, autosomal dominant", "autosomal dominant centronuclear myopathy", "Autosomal dominant centronuclear myopathy", "centronuclear myopathy, autosomal dominant", "Myopathy, Centronuclear, Autosomal Dominant", "myopathy, centronuclear, autosomal dominant", "MYOPATHY, CENTRONUCLEAR, AUTOSOMAL DOMINANT", "centronuclear myopathy, autosomal, modifier of", "Autosomal dominant centronuclear myopathy (disorder)", "autosomal dominant centronuclear myopathy caused by mutation in MYF6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant centronuclear myopathy", "shortest_name_length": 4}
{"curie": "MONDO:0017554", "names": ["radio-ulnar fusion, unilateral", "radio-ulnar synostosis, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radio-ulnar synostosis, unilateral", "shortest_name_length": 30}
{"curie": "MONDO:0014121", "names": ["SMALED2", "SMALED2A", "spinal muscular atrophy with lower extremity predominant 2A", "spinal muscular atrophy with lower extremity predominance 2A", "autosomal dominant spinal muscular atrophy, lower extremity-predominant 2", "spinal muscular atrophy, lower extremity-predominant 2, autosomal dominant", "spinal muscular atrophy, LOWER extremity-predominant, 2, autosomal dominant", "spinal muscular atrophy, lower extremity-predominant, 2A, autosomal dominant", "BICD2-related autosomal dominant childhood-onset proximal spinal muscular atrophy", "autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures", "SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2A, CHILDHOOD ONSET, AUTOSOMAL DOMINANT", "Lower extremity-predominant autosomal dominant proximal spinal muscular atrophy with contractures", "BICD2-related lower extremity-predominant autosomal dominant proximal spinal muscular atrophy with contractures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures", "shortest_name_length": 7}
{"curie": "MONDO:0011300", "names": ["MYP3", "myopia-3", "Myopia 3", "MYOPIA 3 (disorder)", "MYOPIA 3, AUTOSOMAL DOMINANT", "myopia 3, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopia 3, autosomal dominant", "shortest_name_length": 4}
{"curie": "UMLS:C3275163", "names": ["Intrahepatic Bile Duct Microcystic Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intrahepatic Bile Duct Microcystic Adenoma", "shortest_name_length": 42}
{"curie": "MONDO:0014893", "names": ["OCNDS", "Okur-Chung neurodevelopmental syndrome", "OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME", "Okur-Chung neurodevelopmental syndrome; OCNDS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Okur-Chung neurodevelopmental syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C4727396", "names": ["Recurrent Ovarian Serous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Ovarian Serous Adenocarcinoma", "shortest_name_length": 39}
{"curie": "MONDO:0007733", "names": ["HLP3", "HPE3", "Hlp3", "holoprosencephaly 3", "HOLOPROSENCEPHALY 3", "Holoprosencephaly 3", "SHH holoprosencephaly", "Shh holoprosencephaly", "holoprosencephaly type 3", "holoprosencephaly caused by mutation in Shh", "holoprosencephaly caused by mutation in SHH"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "holoprosencephaly 3", "shortest_name_length": 4}
{"curie": "MONDO:0006930", "names": ["pseudobulbar palsy", "Pseudobulbar palsy", "Pseudobulbar Palsy", "PSEUDOBULBAR PALSY", "palsy pseudobulbar", "Palsy, Pseudobulbar", "Pseudobulbar Pareses", "Spastic Bulbar Palsy", "Pseudobulbar Palsies", "Pseudobulbar Paresis", "Pseudobulbar Syndrome", "Palsies, Pseudobulbar", "Bulbar Palsy, Spastic", "Palsy, Spastic Bulbar", "Paresis, Pseudobulbar", "pseudobulbar syndrome", "Pseudobulbar syndrome", "Pareses, Pseudobulbar", "Pseudobulbar Paralysis", "Pseudobulbar Syndromes", "Pseudobulbar Paralyses", "Pseudobulbar paralysis", "PSEUDOBULBAR PARALYSIS", "pseudobulbar paralysis", "Syndrome, Pseudobulbar", "Spastic Bulbar Palsies", "Paralyses, Pseudobulbar", "pseudobulbar; paralysis", "Syndromes, Pseudobulbar", "Bulbar Palsies, Spastic", "paralysis; pseudobulbar", "Palsies, Spastic Bulbar", "Paralysis, Pseudobulbar", "Pseudobulbar palsy (disorder)", "pseudobulbar palsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudobulbar palsy", "shortest_name_length": 18}
{"curie": "UMLS:C4721434", "names": ["Stage IV Larynx Epidermoid Carcinoma", "Stage IV Epidermoid Carcinoma of Larynx", "Stage IV Laryngeal Epidermoid Carcinoma", "Stage IV Larynx Squamous Cell Carcinoma", "Stage IV Squamous Cell Carcinoma of Larynx", "Stage IV Laryngeal Squamous Cell Carcinoma", "Stage IV Epidermoid Carcinoma of the Larynx", "Stage IV Laryngeal Throat Squamous Cell Cancer", "Stage IV Squamous Cell Carcinoma of the Larynx", "Stage IV Laryngeal Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Laryngeal Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 36}
{"curie": "UMLS:C0280383", "names": ["nasopharynx lymphoepithelioma, stage III", "Nasopharyngeal lymphepithelioma stage III", "Nasopharyngeal lymphoepithelioma stage III", "Stage III Nasopharyngeal Lymphoepithelioma", "Stage III Lymphoepithelioma of Nasopharynx", "nasopharyngeal lymphoepithelioma, stage III", "Stage III Lymphoepithelioma of the Nasopharynx", "stage III lymphoepithelioma of the nasopharynx", "lymphoepithelioma of the nasopharynx, stage III", "Stage III Nasopharyngeal Undifferentiated Carcinoma", "Nasopharyngeal Undifferentiated Carcinoma Stage III", "Stage III Undifferentiated Nasopharyngeal Throat Cancer", "Stage III Nasopharyngeal Undifferentiated Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasopharyngeal lymphoepithelioma stage III", "shortest_name_length": 40}
{"curie": "UMLS:C5670380", "names": ["BRANCHING VARIATION", "Vessel Branching Variation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vessel Branching Variation", "shortest_name_length": 19}
{"curie": "MONDO:0016672", "names": ["HPFH-sickle cell disease syndrome", "hereditary persistence of fetal hemoglobin-sickle cell disease syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary persistence of fetal hemoglobin-sickle cell disease syndrome", "shortest_name_length": 33}
{"curie": "MONDO:0020076", "names": ["MPD", "MPN", "CMPD", "CMPD, U", "myeloproliferative tumor", "Myeloproliferative Tumor", "myeloproliferative disease", "Myeloproliferative Disease", "Disease;myeloproliferative", "disease myeloproliferative", "Myeloproliferative disease", "disorder myeloproliferative", "MYELOPROLIFERATIVE DISORDER", "DISORDER MYELOPROLIFERATIVE", "Disorder myeloproliferative", "Myeloproliferative Disorder", "myeloproliferative neoplasm", "myeloproliferative disorder", "Myeloproliferative neoplasm", "Myeloproliferative disorder", "diseases myeloproliferative", "Myeloproliferative Neoplasm", "Myeloproliferative disorders", "myeloproliferative neoplasms", "Myeloproliferative Disorders", "disorders myeloproliferative", "Myeloproliferative neoplasms", "myeloproliferative disorders", "Disorder, Myeloproliferative", "Disorders, Myeloproliferative", "Proliferation of myeloid cells", "Myeloproliferative disease, NOS", "Myeloproliferative disorder NOS", "Myeloproliferative neoplasm, NOS", "Chronic myeloproliferative disease", "chronic myeloproliferative disease", "Chronic Myeloproliferative Disease", "myeloproliferative syndrome chronic", "Chronic Myeloproliferative Disorder", "chronic myeloproliferative disorder", "Chronic Myeloproliferative Neoplasm", "Chronic myeloproliferative disorder", "chronic myeloproliferative syndrome", "chronic myeloproliferative neoplasm", "Chronic Myeloproliferative Disorders", "chronic myeloproliferative neoplasms", "chronic myeloproliferative disorders", "myeloproliferative neoplasm, chronic", "myeloproliferative; disease (chronic)", "Myeloproliferative disorder (disorder)", "Chronic myeloproliferative disease NOS", "Myeloproliferative disease, unspecified", "Chronic myeloproliferative disease, NOS", "Myeloproliferative disease (chronic) NOS", "Myeloproliferative neoplasms (incl. CML)", "Chronic myeloproliferative disorder (clinical)", "chronic myeloproliferative syndrome (diagnosis)", "disease (or disorder); myeloproliferative (chronic)", "Myeloproliferative disorder (morphologic abnormality)", "Chronic myeloproliferative disorder (clinical) (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myeloproliferative neoplasm", "shortest_name_length": 3}
{"curie": "MONDO:0023472", "names": ["impossible syndrome", "chondrodysplasia situs inversus imperforate anus polydactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chondrodysplasia situs inversus imperforate anus polydactyly", "shortest_name_length": 19}
{"curie": "UMLS:C1504403", "names": ["Acute lymphocytic leukemia recurrent", "Acute lymphocytic leukaemia recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute lymphocytic leukemia recurrent", "shortest_name_length": 36}
{"curie": "MONDO:0010740", "names": ["taurodontism, microdontia, and dens invaginatus", "TAURODONTISM, MICRODONTIA, AND DENS INVAGINATUS", "Taurodontism, microdontia, and dens invaginatus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "taurodontism, microdontia, and dens invaginatus", "shortest_name_length": 47}
{"curie": "MONDO:0008711", "names": ["ACPS4", "ACPS 4", "ACPS IV", "GOODMAN SYNDROME", "Goodman syndrome", "Goodman camptodactyly", "Acrocephalosyndactyly, type IV", "Acrocephalopolysyndactyly type 4", "acrocephalopolysyndactyly type 4", "Acrocephalopolysyndactyly Type IV", "acrocephalopolysyndactyly type IV", "ACROCEPHALOPOLYSYNDACTYLY TYPE IV", "Acrocephalopolysyndactyly type IV", "Acrocephalopolysyndactyly type IV (disorder)", "Camptodactyly-fibrous tissue hyperplasia-skeletal anomalies syndrome", "Camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia syndrome", "Camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Goodman syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0019461", "names": ["BPLL", "B-PLL", "B Prolymphocytic Leukemia", "B prolymphocytic leukemia", "B-Cell Prolymphocytic Leukemia", "B Cell Prolymphocytic Leukemia", "B-cell prolymphocytic leukemia", "Leukemia, B-Cell Prolymphocytic", "Prolymphocytic Leukemia, B-Cell", "B-Cell Prolymphocytic Leukemias", "B-cell prolymphocytic leukaemia", "Prolymphocytic Leukemias, B-Cell", "Leukemia, Prolymphocytic, B-Cell", "Leukemias, B-Cell Prolymphocytic", "leukemia prolymphocytic B-cell type", "B-cell type prolymphocytic leukemia", "Prolymphocytic leukemia, B-cell type", "Prolymphocytic leukaemia, B-cell type", "Prolymphocytic leukemia of B-cell type", "B-cell prolymphocytic leukemia (disorder)", "Prolymphocytic leukemia of B-cell type NOS", "B-cell prolymphocytic leukemia (diagnosis)", "Prolymphocytic leukemia, B-cell type (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B-cell prolymphocytic leukemia", "shortest_name_length": 4}
{"curie": "MONDO:0020470", "names": ["49,XYYYY syndrome", "49,XYYYY syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "49,XYYYY syndrome", "shortest_name_length": 17}
{"curie": "MONDO:0014995", "names": ["NDHSAL", "NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE", "neurodevelopmental disorder with hypotonia, seizures, and absent language", "neurodevelopmental disorder with hypotonia, seizures, and absent language; NDHSAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder with hypotonia, seizures, and absent language", "shortest_name_length": 6}
{"curie": "MONDO:0044843", "names": ["Torsion dystonia", "torsion dystonia", "Dystonia musculorum deformans"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "torsion dystonia", "shortest_name_length": 16}
{"curie": "UMLS:C0004044", "names": ["ASPHYXIA", "Asphyxia", "asphyxia", "asphyxias", "suffocate", "Asphyxias", "suffocating", "Suffocating", "Suffocation", "suffocation", "Suffocations", "asphyxiation", "Asphyxiation", "ASPHYXIATION", "suffocations", "Suffocation NOS", "Suffocation, NOS", "Asphyxiation, NOS", "asphyxia (diagnosis)", "Asphyxiation (event)", "Suffocating (finding)", "suffocation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Asphyxia", "shortest_name_length": 8}
{"curie": "UMLS:C4688354", "names": ["Recurrent Craniopharyngioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Craniopharyngioma", "shortest_name_length": 27}
{"curie": "UMLS:C5669772", "names": ["Diffuse Low Grade Glioma, BRAF p.V600E-Mutant", "Diffuse Low-Grade Glioma, BRAF p.V600E Mutant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse Low Grade Glioma, BRAF p.V600E-Mutant", "shortest_name_length": 45}
{"curie": "MONDO:0011234", "names": ["ARCND1", "auriculocondylar syndrome 1", "question Mark ears syndrome", "AURICULOCONDYLAR syndrome 1", "AURICULOCONDYLAR SYNDROME 1", "Auriculocondylar syndrome 1", "GNAI3 auriculocondylar syndrome", "Auriculocondylar syndrome type 1", "auriculocondylar syndrome caused by mutation in GNAI3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "auriculocondylar syndrome 1", "shortest_name_length": 6}
{"curie": "MONDO:0010210", "names": ["XPA", "XP1", "XP-A", "XP group A", "XP, group A", "XP, GROUP A", "XERODERMA PIGMENTOSUM I", "xeroderma pigmentosum 1", "XPA xeroderma pigmentosum", "xeroderma pigmentosum, type 1", "Xeroderma pigmentosum group A", "Xeroderma Pigmentosum Group A", "xeroderma pigmentosum group A", "Xeroderma pigmentosum, group A", "xeroderma pigmentosum, group A", "xeroderma pigmentosum group type A", "Xeroderma pigmentosum, group A (disorder)", "xeroderma pigmentosum complementation group A", "Xeroderma Pigmentosum, Complementation Group A", "xeroderma pigmentosum, complementation group A", "XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A", "xeroderma pigmentosum caused by mutation in XPA", "xeroderma pigmentosum, complementation group type a"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "xeroderma pigmentosum group A", "shortest_name_length": 3}
{"curie": "MONDO:0012385", "names": ["Cupped metaphyses and cone-shaped epiphyses without alopecia or brachydactyly", "cupped metaphyses and cone-Shaped epiphyses without alopecia or brachydactyly", "CUPPED METAPHYSES AND CONE-SHAPED EPIPHYSES WITHOUT ALOPECIA OR BRACHYDACTYLY", "METAPHYSEAL CHONDRODYSPLASIA WITH CONE-SHAPED EPIPHYSES, NORMAL HAIR, AND NORMAL HANDS", "Metaphyseal chondrodysplasia with cone-shaped epiphyses, normal hair, and normal hands", "metaphyseal chondrodysplasia with cone-shaped epiphyses, normal hair, and normal hands"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metaphyseal chondrodysplasia with cone-shaped epiphyses, normal hair, and normal hands", "shortest_name_length": 77}
{"curie": "EFO:0009094", "names": ["idiopathic dilated cardiomyopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic dilated cardiomyopathy", "shortest_name_length": 33}
{"curie": "UMLS:C2211707", "names": ["Breast Carcinoma with Neuroendocrine Differentiation", "breast adenocarcinoma with neuroendocrine differentiation", "Breast Adenocarcinoma with Neuroendocrine Differentiation", "adenocarcinoma of breast with neuroendocrine differentiation", "adenocarcinoma of breast with neuroendocrine differentiation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenocarcinoma of breast with neuroendocrine differentiation", "shortest_name_length": 52}
{"curie": "UMLS:C0152442", "names": ["Comedomastitis", "comedomastitis", "breast; ectasia", "ectasia; breast", "breast duct ectasia", "duct ectasia breast", "mammary duct ectasia", "Mammary duct ectasia", "Mammary Duct Ectasia", "mammary duct; ectasia", "ectasia; mammary duct", "Duct ectasia of breast", "Ectasia of Mammary Duct", "mammary duct; dilatation", "dilatation; mammary duct", "Ectasia of the Mammary Duct", "Mammary duct ectasia (disorder)", "mammary duct ectasia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mammary duct ectasia", "shortest_name_length": 14}
{"curie": "MONDO:0020390", "names": ["pulmonary artery coming from patent ductus arteriosus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary artery coming from patent ductus arteriosus", "shortest_name_length": 53}
{"curie": "UMLS:C0333871", "names": ["Moderate Squamous Cell Atypia", "Moderate squamous cell atypia", "Moderate squamous cell atypia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Moderate squamous cell atypia", "shortest_name_length": 29}
{"curie": "MONDO:0009252", "names": ["fructosuria", "Fructosuria", "Benign fructosemia", "Benign fructosaemia", "disorder fructosuria", "Essential fructosemia", "essential fructosuria", "Essential fructosuria", "FRUCTOSURIA, ESSENTIAL", "Essential fructosaemia", "fructosuria, essential", "Fructosuria (disorder)", "Fructokinase deficiency", "fructokinase deficiency", "deficiency; fructokinase", "fructokinase; deficiency", "KETOHEXOKINASE DEFICIENCY", "Ketohexokinase deficiency", "ketohexokinase deficiency", "Deficiency of fructokinase", "EF - Essential fructosemia", "EF - Essential fructosaemia", "Deficiency of ketohexokinase", "Essential benign fructosuria", "essential benign fructosuria", "HEPATIC FRUCTOKINASE DEFICIENCY", "Hepatic fructokinase deficiency", "hepatic fructokinase deficiency", "Deficiency of fructokinase (disorder)", "Deficiency of ketohexokinase (disorder)", "essential benign fructosuria (diagnosis)", "Hepatic fructokinase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "essential fructosuria", "shortest_name_length": 11}
{"curie": "MONDO:0025159", "names": ["swine enzootic pneumonia", "Swine Enzootic Pneumonia", "enzootic pneumonia of pigs", "Swine Mycoplasma Pneumonia", "Enzootic Pneumonia of Pigs", "swine Mycoplasma pneumonia", "swine Mycoplasmal pneumonia", "Swine Mycoplasmal Pneumonia", "enzootic pneumonia of swine", "Enzootic Pneumonia of Swine", "pneumonia of swine, enzootic", "Mycoplasma Pneumonia of Pigs", "Mycoplasma pneumonia of pigs", "Pneumonia of Swine, Enzootic", "Mycoplasma Pneumonia of Swine", "Mycoplasma pneumonia of swine", "Mycoplasmal Pneumonia of Swine", "Mycoplasmal pneumonia of swine", "pneumonia of swine, mycoplasmal", "Pneumonia of Swine, Mycoplasmal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pneumonia of swine, mycoplasmal", "shortest_name_length": 24}
{"curie": "UMLS:C1707319", "names": ["Cavernous Angioleiomyoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cavernous Angioleiomyoma", "shortest_name_length": 24}
{"curie": "MONDO:0037940", "names": ["inherited auditory system disease", "hereditary auditory system disease", "auditory system hereditary disorder", "Auditory system hereditary disorder", "Auditory system hereditary disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited auditory system disease", "shortest_name_length": 33}
{"curie": "MONDO:0004904", "names": ["Toxic maculopathy", "toxic maculopathy", "maculopathy; toxic", "Toxic maculopathy of retina", "toxic maculopathy of retina", "Toxic maculopathy (disorder)", "toxic maculopathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "toxic maculopathy", "shortest_name_length": 17}
{"curie": "MONDO:0016761", "names": ["SED", "SED and SEMD", "spondyloepiphyseal dysplasia", "spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondyloepiphyseal dysplasia", "shortest_name_length": 3}
{"curie": "UMLS:C0862836", "names": ["Lung carcinoma stage II", "Carcinoma of lung stage II", "Pulmonary carcinoma stage II", "Carcinoma lung cell type unspecified stage II", "Lung carcinoma cell type unspecified stage II", "Pulmonary carcinoma cell type unspecified stage II"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung carcinoma cell type unspecified stage II", "shortest_name_length": 23}
{"curie": "UMLS:C5420191", "names": ["Tongue Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tongue Liposarcoma", "shortest_name_length": 18}
{"curie": "UMLS:C1868889", "names": ["Constipation predominant irritable bowel syndrome", "Irritable bowel syndrome characterised by constipation", "Irritable bowel syndrome characterized by constipation", "Irritable bowel syndrome characterized by constipation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Irritable bowel syndrome characterized by constipation", "shortest_name_length": 49}
{"curie": "UMLS:C5420772", "names": ["Conjunctival Stromal Nevus", "Conjunctival Subepithelial Nevus", "Conjunctival Subepithelial (Stromal) Nevus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conjunctival Subepithelial Nevus", "shortest_name_length": 26}
{"curie": "UMLS:C0412850", "names": ["Opioid toxicity", "opioid toxicity", "toxicity from opioids", "opioid toxicity (diagnosis)", "Poisoning by opiate analgesic drug"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Opioid toxicity", "shortest_name_length": 15}
{"curie": "MONDO:0014973", "names": ["SCFI", "sudden Cardiac failure, infantile", "sudden cardiac failure, infantile", "SUDDEN CARDIAC FAILURE, INFANTILE", "sudden cardiac failure, infantile; SCFI"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sudden cardiac failure, infantile", "shortest_name_length": 4}
{"curie": "MONDO:0019149", "names": ["CESD", "CHOLESTERYL ESTER STORAGE DISEASE", "Cholesterol Ester Storage Disease", "Cholesterol ester storage disease", "cholesteryl ester storage disease", "cholesterol ester storage disease", "Cholesteryl ester storage disease", "Cholesteryl Ester Storage Disease", "CESD - Cholesterol ester storage disease", "Cholesterol ester storage disease (disorder)", "cholesterol ester storage disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholesteryl ester storage disease", "shortest_name_length": 4}
{"curie": "UMLS:C1708173", "names": ["Gallbladder Flat BilIN", "Gallbladder Flat Intraepithelial Neoplasia", "Gallbladder Flat Biliary Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gallbladder Flat Biliary Intraepithelial Neoplasia", "shortest_name_length": 22}
{"curie": "MONDO:0009508", "names": ["Lambotte syndrome", "LAMBOTTE SYNDROME", "Microcephaly, holoprosencephaly, and intrauterine growth retardation", "MICROCEPHALY, HOLOPROSENCEPHALY, AND INTRAUTERINE GROWTH RETARDATION", "microcephaly, holoprosencephaly, and intrauterine Growth retardation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lambotte syndrome", "shortest_name_length": 17}
{"curie": "MONDO:0008669", "names": ["vulvovaginitis, allergic seminal", "VULVOVAGINITIS, ALLERGIC SEMINAL", "Vulvovaginitis, Allergic Seminal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvovaginitis, allergic seminal", "shortest_name_length": 32}
{"curie": "MONDO:0001246", "names": ["shop", "TYPHUS", "Typhus", "typhus", "jail fever", "Typhus NOS", "ship fever", "RAT TYPHUS", "Ship fever", "Jail fever", "shop typhus", "Typhus, NOS", "typhus; rat", "Flea typhus", "flea typhus", "Shop typhus", "rat; typhus", "FLEA TYPHUS", "Famine fever", "famine fever", "typhus fever", "Urban typhus", "prison fever", "fever typhus", "Prison fever", "typhus; shop", "shop; typhus", "Typhus fever", "Murine Typhus", "murine typhus", "MURINE TYPHUS", "Murine typhus", "Moscow typhus", "Typhus, murine", "typhus; murine", "hospital fever", "Endemic typhus", "murine; typhus", "Mexican typhus", "Endemic Typhus", "Typhus, Murine", "Hospital fever", "endemic typhus", "typhus; endemic", "TYPHUS, ENDEMIC", "Petechial fever", "rat flea typhus", "Rat flea typhus", "endemic; typhus", "petechial fever", "Typhus, Endemic", "European typhus", "Flea-born typhus", "classical typhus", "Classical typhus", "Typhus fever NOS", "flea-borne typhus", "Flea-borne typhus", "Typhus infections", "Flea-borne Typhus", "typhus (diagnosis)", "louse-borne typhus", "Louse-borne typhus", "typhus; flea-borne", "flea-borne; typhus", "Typhus (fever) NOS", "Typhus, unspecified", "Endemic Typhus fever", "Exanthematous typhus", "Endemic Typhus Fever", "endemic typhus fever", "exanthematous typhus", "endemic murine typhus", "typhus exanthematique", "Typhus exanthematique", "Endemic murine typhus", "SHOP TYPHUS OF MALAYA", "tabardillo; flea-borne", "flea-borne; tabardillo", "Murine (endemic) typhus", "murine [endemic] typhus", "Murine Typhus Infection", "Murine [endemic] typhus", "Flea-borne Typhus fever", "Murine Typhus Infections", "Infection, Murine Typhus", "Typhus Infection, Murine", "classical typhus (fever)", "Flea-borne rickettsiosis", "flea-borne rickettsiosis", "Murine typhus (disorder)", "louse-borne rickettsiosis", "exanthematic typhus fever", "Typhus Infections, Murine", "Exanthematic Typhus fever", "murine typhus (diagnosis)", "endemic flea-borne typhus", "Endemic Flea-Borne Typhus", "Typhus fever, unspecified", "Infections, Murine Typhus", "Louse-borne rickettsiosis", "Typhus, Endemic flea-borne", "rickettsia typhi infection", "Flea-Borne Typhus, Endemic", "typhus-group rickettsiosis", "Rickettsia typhi Infection", "Rickettsia typhi infection", "Typhus, Endemic Flea Borne", "murine endemic flea typhus", "Murine endemic flea typhus", "Typhus-group rickettsiosis", "Typhus, Endemic Flea-Borne", "Rickettsia typhi Infections", "epidemic louse-borne typhus", "Infection, Rickettsia typhi", "Infections, Rickettsia typhi", "Louse-borne [epidemic] typhus", "louse-borne [epidemic] typhus", "epidemic (louse-borne) typhus", "Epidemic (louse-borne) typhus", "Typhus due to Rickettsia typhi", "rickettsiosis; Rickettsia typhi", "typhi; Rickettsia typhi, typhus", "Typhus group rickettsial disease", "Typhus-group rickettsiae disease", "typhus-group rickettsiae disease", "Typhus fever due to Rickettsia typhi", "Typhus group rickettsial disease (disorder)", "Epidemic louse-borne typhus fever due to Rickettsia prowazekii", "epidemic louse-borne typhus fever due to Rickettsia prowazekii"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "typhus", "shortest_name_length": 4}
{"curie": "UMLS:C3828506", "names": ["Postpartum Obstetric Septic Embolism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postpartum Obstetric Septic Embolism", "shortest_name_length": 36}
{"curie": "UMLS:C1334430", "names": ["Low Risk Esophageal GIST", "Low Risk Esophageal Gastrointestinal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Low Risk Esophageal Gastrointestinal Stromal Tumor", "shortest_name_length": 24}
{"curie": "UMLS:C0271066", "names": ["Subretinal neovascularization", "Subretinal neovascularisation", "Choroidal neovascular membrane", "CNV - Choroidal neovascularisation", "SRNV-Subretinal neovascularization", "CNV - Choroidal neovascularization", "SRNV-Subretinal neovascularisation", "Choroidal retinal neovascularisation", "retinal neovascularization choroidal", "Choroidal retinal neovascularization", "CNVM - Choroidal neovascular membrane", "Choroidal retinal neovascularization (disorder)", "Choroidal retinal neovascularization (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Choroidal retinal neovascularization", "shortest_name_length": 29}
{"curie": "MONDO:0018434", "names": ["AML with t(9;11)(p22;q23)", "acute myeloid leukemia with t(9;11)(p22;q23)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia with t(9;11)(p22;q23)", "shortest_name_length": 25}
{"curie": "UMLS:C1336295", "names": ["Stage II Lip Cancer", "Stage II Cancer of Lip", "Stage II Lip Carcinoma", "Stage II Carcinoma of Lip", "Stage II Cancer of the Lip", "Stage II Lip Cancer AJCC v7", "Stage II Lip Cancer AJCC v6", "Stage II Carcinoma of the Lip", "Stage II Lip Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Lip Cancer AJCC v6 and v7", "shortest_name_length": 19}
{"curie": "MONDO:0009138", "names": ["dysosteosclerosis", "DYSOSTEOSCLEROSIS", "Dysosteosclerosis", "dysosteosclerosis (DOS)", "Dysosteosclerosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dysosteosclerosis", "shortest_name_length": 17}
{"curie": "MONDO:0006288", "names": ["pheochromoblastoma", "Pheochromoblastoma", "Phaeochromoblastoma", "Malignant Pheochromocytoma", "malignant pheochromocytoma", "Malignant pheochromocytoma", "Pheochromocytoma malignant", "pheochromocytoma, malignant", "Phaeochromocytoma malignant", "Malignant phaeochromocytoma", "PHEOCHROMOCYTOMA, MALIGNANT", "Metastatic Pheochromocytoma", "Pheochromocytoma, malignant", "Phaeochromocytoma, malignant", "Malignant Adrenal Pheochromocytoma", "malignant adrenal pheochromocytoma", "Malignant Adrenal Gland Paraganglioma", "malignant adrenal gland Chromaffinoma", "Malignant pheochromocytoma (disorder)", "malignant adrenal gland paraganglioma", "Malignant Adrenal Gland Chromaffinoma", "malignant pheochromocytoma (diagnosis)", "malignant adrenal gland chromaffin tumor", "malignant paraganglioma of adrenal gland", "Malignant Adrenal Gland Pheochromocytoma", "malignant adrenal gland pheochromocytoma", "Malignant Adrenal Gland Chromaffin Tumor", "Metastatic Adrenal Gland Pheochromocytoma", "adrenal gland pheochromocytoma, malignant", "malignant adrenal medullary paraganglioma", "Malignant Adrenal Medullary Paraganglioma", "Adrenal medullary paraganglioma, malignant", "malignant pheochromocytoma of adrenal gland", "Malignant Adrenal Gland Chromaffin Neoplasm", "malignant adrenal gland chromaffin neoplasm", "Malignant Adrenal Medullary Pheochromocytoma", "malignant adrenal medullary pheochromocytoma", "malignant; pheochromocytoma, unspecified site", "pheochromocytoma; malignant, unspecified site", "malignant adrenal gland chromaffin paraganglioma", "Malignant Adrenal Gland Chromaffin Paraganglioma", "malignant paraganglioma of adrenal gland (diagnosis)", "Malignant pheochromocytoma (morphologic abnormality)", "malignant pheochromocytoma of adrenal gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant adrenal gland pheochromocytoma", "shortest_name_length": 18}
{"curie": "MONDO:0014653", "names": ["RP72", "RETINITIS PIGMENTOSA 72", "retinitis pigmentosa 72", "ZNF408 retinitis pigmentosa", "retinitis pigmentosa type 72", "retinitis pigmentosa caused by mutation in ZNF408"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 72", "shortest_name_length": 4}
{"curie": "MONDO:0019862", "names": ["Levocardia", "LEVOCARDIA", "levocardia", "Laevocardia", "Sinistrocardia", "Levocardia, NOS", "Left sided heart", "Isolated Levocardia", "Isolated levocardia", "Sinistrocardia, NOS", "Isolated laevocardia", "Levocardia, Isolated", "Levocardia, isolated", "levocardia (diagnosis)", "Isolated sinistrocardia", "Sinistrocardia, isolated", "levocardia-situs inversus", "Situs inversus with levocardia", "Situs Inversus with Levocardia", "Levocardia with situs inversus", "Situs inversus with laevocardia", "Heart predominantly in left hemithorax", "Isolated levocardia with situs inversus", "Situs inversus with levocardia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "levocardia", "shortest_name_length": 10}
{"curie": "MONDO:0017866", "names": ["subpulmonary stenosis", "Subpulmonary stenosis", "Subpulmonary stenosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subpulmonary stenosis", "shortest_name_length": 21}
{"curie": "UMLS:C1699730", "names": ["Fistula of small intestine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fistula of small intestine", "shortest_name_length": 26}
{"curie": "MONDO:0007569", "names": ["Familial erythema nodosum", "familial erythema nodosum", "erythema nodosum, familial", "Erythema nodosum, familial", "ERYTHEMA NODOSUM, FAMILIAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythema nodosum, familial", "shortest_name_length": 25}
{"curie": "MONDO:0003849", "names": ["clival chordoma", "Clival Chordoma", "clivus chordoma", "Clivus Chordoma", "Chordoma of clivus", "Chordoma of Clivus", "chordoma of clivus", "chordoma of the clivus", "Chordoma of the Clivus", "Chordoma of clivus (disorder)", "chordoma of clivus (diagnosis)", "clivus of occipital bone chordoma (disease)", "chordoma (disease) of clivus of occipital bone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "clivus chordoma", "shortest_name_length": 15}
{"curie": "MONDO:0023196", "names": ["frontonasal malformation cloacal exstrophy", "fronto nasal malformation cloacal exstrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontonasal malformation cloacal exstrophy", "shortest_name_length": 42}
{"curie": "UMLS:C0271560", "names": ["lymphocytic hypophysitis", "Lymphocytic hypophysitis", "Lymphocytic hypopituitarism", "lymphocytic hypophysitis (diagnosis)", "Lymphocytic hypopituitarism (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphocytic hypopituitarism", "shortest_name_length": 24}
{"curie": "UMLS:C0041274", "names": ["Tubal block", "tubal block", "tubal; block", "block; tubal", "Tubal Obstruction", "tubal obstruction", "Obstruction, Tubal", "Obstructed oviduct", "Tubal Obstructions", "Obstructions, Tubal", "Obstruction of oviduct", "blocked fallopian tube", "Blocked fallopian tube", "blocked fallopian tubes", "Fallopian tube obstruction", "blockage of fallopian tube", "fallopian obstruction tube", "Fallopian Tube Obstruction", "fallopian tube obstruction", "FALLOPIAN TUBE OBSTRUCTION", "fallopian tube; obstruction", "fallopian obstruction tubes", "obstruction; fallopian tube", "Blocked fallopian tube (disorder)", "blockage of fallopian tube (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fallopian tube obstruction", "shortest_name_length": 11}
{"curie": "MONDO:0000299", "names": ["thelaziosis", "Thelaziasis", "thelaziasis", "Thelaziosis", "verminous ophthalmia", "Verminous ophthalmia", "Infection by Thelazia", "infection by Thelazia", "conjunctival spirurosis", "thelaziasis (diagnosis)", "Conjunctival spirurosis", "Infection by Thelazia, NOS", "Thelazia infectious disease", "Thelazia disease or disorder", "infection caused by Thelazia", "Infection caused by Thelazia", "Thelazia caused disease or disorder", "Infection caused by Thelazia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thelaziasis", "shortest_name_length": 11}
{"curie": "MONDO:0009432", "names": ["hypopituitarism, congenital, with central diabetes insipidus", "Hypopituitarism, Congenital, with Central Diabetes Insipidus", "HYPOPITUITARISM, CONGENITAL, WITH CENTRAL DIABETES INSIPIDUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypopituitarism, congenital, with central diabetes insipidus", "shortest_name_length": 60}
{"curie": "UMLS:C1096091", "names": ["Infusion site itching", "Infusion site pruritus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infusion site pruritus", "shortest_name_length": 21}
{"curie": "UMLS:C5419029", "names": ["Refractory Extrarenal Rhabdoid Tumor of the Ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Extrarenal Rhabdoid Tumor of the Ovary", "shortest_name_length": 49}
{"curie": "MONDO:0012297", "names": ["SPOAN", "SPOAN syndrome", "spastic paraplegia, optic atropy, and neuropathy", "SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND NEUROPATHY", "Spastic Paraplegia, Optic Atrophy, and Neuropathy", "spastic paraplegia, optic atrophy, and neuropathy", "Spastic paraplegia-optic atrophy-neuropathy syndrome", "spastic paraplegia-optic atrophy-neuropathy syndrome", "Spastic paraplegia, optic atrophy, neuropathy syndrome", "spastic paraplegia, optic atropy, and neuropathy syndrome", "SPOAN (spastic paraplegia, optic atrophy, neuropathy) syndrome", "Spastic paraplegia, optic atrophy, neuropathy syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SPOAN syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0017895", "names": ["FNMTC", "NSFNMTC", "Non-Syndromic Familial Thyroid Cancer", "Familial nonmedullary thyroid carcinoma", "Familial non medullary thyroid carcinoma", "familial pure nonmedullary thyroid carcinoma", "Familial pure nonmedullary thyroid carcinoma", "familial nonmedullary thyroid gland carcinoma", "Familial Nonmedullary Thyroid Gland Carcinoma", "Familial Non-medullary Thyroid Gland Carcinoma", "FNMTC - familial nonmedullary thyroid carcinoma", "familial papillary or follicular thyroid carcinoma", "Familial papillary or follicular thyroid carcinoma", "Familial nonmedullary thyroid carcinoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial papillary or follicular thyroid carcinoma", "shortest_name_length": 5}
{"curie": "UMLS:C2347762", "names": ["Teratoma", "childhood teratoma", "Childhood Teratoma", "childhood mature and immature teratomas", "pediatric mature and immature teratomas", "mature and immature teratomas, childhood", "mature and immature teratomas, pediatric"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Teratoma", "shortest_name_length": 8}
{"curie": "UMLS:C4518436", "names": ["Anaplastic lymphoma kinase positive anaplastic large cell lymphoma", "Anaplastic large cell lymphoma, ALK (anaplastic lymphoma kinase) positive", "Anaplastic lymphoma kinase positive anaplastic large cell lymphoma (disorder)", "Anaplastic lymphoma kinase positive anaplastic large cell lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anaplastic lymphoma kinase positive anaplastic large cell lymphoma", "shortest_name_length": 66}
{"curie": "UMLS:C0271912", "names": ["aplastic anemia due to infection", "Aplastic anemia due to infection", "Aplastic Anemia due to Infection", "Aplastic anaemia due to infection", "anemia; aplastic, due to infection", "aplastic; anemia, due to infection", "Aplastic anemia secondary to infection", "Aplastic anaemia secondary to infection", "Aplastic anemia due to infection (disorder)", "aplastic anemia due to infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aplastic anemia due to infection", "shortest_name_length": 32}
{"curie": "MONDO:0010827", "names": ["RP14", "RP 14", "Retinitis Pigmentosa 14", "retinitis pigmentosa 14", "RETINITIS PIGMENTOSA 14", "TULP1 retinitis pigmentosa", "retinitis pigmentosa type 14", "RETINITIS PIGMENTOSA, JUVENILE, TULP1-RELATED", "Retinitis Pigmentosa, Juvenile, TULP1-Related", "retinitis pigmentosa caused by mutation in TULP1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 14", "shortest_name_length": 4}
{"curie": "UMLS:C4520841", "names": ["M6B", "M6b", "PEL", "Erythremic Myelosis", "Di Guglielmo disease", "Di Guglielmo Disease", "Di Guglielmo's Disease", "Pure erythroid leukemia", "Pure Erythroid Leukemia", "Pure erythroid leukaemia", "Acute erythremic myelosis", "Acute Erythremic Myelosis", "Acute Myeloid Leukemia M6b"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pure Erythroid Leukemia", "shortest_name_length": 3}
{"curie": "MONDO:0019498", "names": ["Jigger", "jiggers", "Jiggers", "Tungiasis", "Niguiasis", "tungiasis", "S penetrans", "T penetrans", "chigger flea", "chigoe; chigo", "Sarcopsyllosis", "jigger disease", "Jigger disease", "Chigoe disease", "jigger; disease", "Tunga penetrans", "jigger; chigger", "infestation; chigo", "chigo; infestation", "Chigoe infestation", "Jiggers infestation", "infestation; sandflea", "sandflea; infestation", "Sarcopsylla penetrans", "Infestation by chigoe", "Sand flea infestation", "tungiasis (diagnosis)", "chigger; meaning Jigger", "Infestation by sand flea", "infestation by sand fleas", "Tunga penetrans infection", "jigger disease (diagnosis)", "Tunga penetrans infestation", "infestation; Tunga penetrans", "Tunga penetrans; infestation", "disease (or disorder); jigger", "Infestation by Tunga penetrans", "Tungiasis (sandflea) infestation", "Tungiasis [sandflea infestation]", "Tunga penetrans infectious disease", "Tunga penetrans disease or disorder", "infestation by sand fleas (diagnosis)", "Tunga penetrans infestation (disorder)", "Tunga penetrans caused disease or disorder", "disease (or disorder); chigoe, chigo, chigoe"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tungiasis", "shortest_name_length": 6}
{"curie": "UMLS:C5420405", "names": ["Maxillofacial Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Maxillofacial Sarcoma", "shortest_name_length": 21}
{"curie": "MONDO:0023880", "names": ["WHIM syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "WHIM syndrome", "shortest_name_length": 13}
{"curie": "UMLS:C5205387", "names": ["Advanced Esophageal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Esophageal Carcinoma", "shortest_name_length": 29}
{"curie": "UMLS:C0262593", "names": ["Peripheral Nerve Injury", "Peripheral nerve injury", "peripheral nerve injury", "injury nerve peripheral", "PERIPHERAL NERVE INJURY", "Injury;nerve;peripheral", "Nerve Injury, Peripheral", "Nerve injury, peripheral", "Peripheral nerve injuries", "injury; nerve, peripheral", "peripheral nerve injuries", "nerve; injury, peripheral", "Peripheral Nervous Injury", "Peripheral Nerve Injuries", "Injury of peripheral nerve", "injury of peripheral nerve", "Nerve Injuries, Peripheral", "Peripheral nerve injury, NOS", "PNI - Peripheral nerve injury", "Injury of peripheral nerve (disorder)", "injury of peripheral nerve (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peripheral Nerve Injuries", "shortest_name_length": 23}
{"curie": "MONDO:0044324", "names": ["ALKAS", "AL KAISSI SYNDROME", "Al Kaissi syndrome", "AL KAISSI syndrome", "GROWTH RETARDATION, SPINE MALFORMATION, DYSMORPHIC FACIES, AND DEVELOPMENTAL DELAY", "Growth retardation, spine malformation, dysmorphic facies, and developmental delay"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Al Kaissi syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0016005", "names": ["Fetal indomethacin syndrome", "fetal indomethacin syndrome", "indomethacin embryofetopathy", "Foetal indomethacin syndrome", "Indomethacin embryofetopathy", "antenatal indomethacin exposure", "Embryofetopathy caused by indomethacin", "Embryofetopathy caused by indomethacin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "indomethacin embryofetopathy", "shortest_name_length": 27}
{"curie": "UMLS:C4683020", "names": ["Stage IV Eyelid Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Eyelid Carcinoma AJCC v8", "shortest_name_length": 33}
{"curie": "MONDO:0014441", "names": ["BBS13", "BARDET-BIEDL SYNDROME 13", "Bardet-Biedl syndrome 13", "Bardet-Biedl Syndrome 13", "MKS1 Bardet-Biedl syndrome", "Bardet-Biedl syndrome type 13", "Bardet-Biedl syndrome caused by mutation in MKS1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bardet-Biedl syndrome 13", "shortest_name_length": 5}
{"curie": "UMLS:C0007297", "names": ["Carsickness", "carsickness", "CAR SICKNESS", "Car sickness", "Car Sickness", "car sickness", "Sickness, Car", "Car sickness (finding)", "disease (or disorder); car sickness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carsickness", "shortest_name_length": 11}
{"curie": "MONDO:0005717", "names": ["ORF", "orf", "Orf", "sheep pox", "scabby mouth", "thistle disease", "Orf virus disease", "Sore mouth [ovine]", "Sore mouth (ovine)", "Contagious Ecthyma", "contagious ecthyma", "Contagious ecthyma", "ECTHYMA INFECTIOSUM", "ECTHYMA CONTAGIOSUM", "Ecthyma, Contagious", "Ecthyma contagiosum", "Orf Virus Infection", "ecthyma contagiosum", "ecthyma, Contagious", "infectiosum; ecthyma", "Virus Infection, Orf", "ecthyma; infectiosum", "ecthyma; contagiosum", "Orf Virus Infections", "contagiosum; ecthyma", "Infection, Orf Virus", "Virus Infections, Orf", "Infections, Orf Virus", "Contagious ovine ecthyma", "Bovine pustular stomatitis", "Contagious ecthyma of sheep", "Orf virus disease (disorder)", "Orf virus disease (diagnosis)", "Contagious pustular dermatitis", "Contagious Pustular Dermatitis", "Contagious pustular stomatitis", "contagious pustular dermatitis", "Pustular Dermatitis, Contagious", "Dermatitis, Contagious Pustular", "DERMATITIS, PUSTULAR, CONTAGIOUS", "Contagious Pustular Dermatitides", "Pustular Dermatitides, Contagious", "Dermatitides, Contagious Pustular", "Bovine pustular stomatitis virus infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "contagious pustular dermatitis", "shortest_name_length": 3}
{"curie": "MONDO:0000310", "names": ["Alkhurma hemorrhagic fever", "Alkhumra hemorrhagic fever virus infectious disease", "Alkhumra hemorrhagic fever virus disease or disorder", "Alkhumra hemorrhagic fever virus caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alkhurma hemorrhagic fever", "shortest_name_length": 26}
{"curie": "UMLS:C5447415", "names": ["NDAS", "IKBKG/NEMO NDAS", "NEMO Deleted Exon 5 Autoinflammatory Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "NEMO Deleted Exon 5 Autoinflammatory Syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C1332996", "names": ["B Lymphoblastic Lymphoma", "Childhood B Lymphoblastic Lymphoma", "Childhood B-Lymphoblastic Lymphoma", "Childhood Precursor B-Lymphoblastic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood B Lymphoblastic Lymphoma", "shortest_name_length": 24}
{"curie": "MONDO:0009684", "names": ["MUSCULAR HYPERTONIA, LETHAL", "Muscular Hypertonia, Lethal", "muscular hypertonia, lethal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular hypertonia, lethal", "shortest_name_length": 27}
{"curie": "MONDO:0012837", "names": ["IBD15", "inflammatory bowel disease 15", "INFLAMMATORY BOWEL DISEASE 15", "Inflammatory Bowel Disease 15", "inflammatory bowel disease type 15"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory bowel disease 15", "shortest_name_length": 5}
{"curie": "UMLS:C0852977", "names": ["Aggravated Epilepsy", "Epilepsy aggravated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epilepsy aggravated", "shortest_name_length": 19}
{"curie": "MONDO:0019922", "names": ["UPD(7)pat", "Paternal uniparental disomy of chromosome 7", "paternal uniparental disomy of chromosome 7", "paternal uniparental disomy of chromosome type 7", "Paternal uniparental disomy of chromosome 7 (disorder)", "Paternal uniparental disomy of chromosome 7 (diagnosis)", "anomaly of chromosome pair paternal uniparental disomy chromosome 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paternal uniparental disomy of chromosome 7", "shortest_name_length": 9}
{"curie": "MONDO:0004752", "names": ["Heart Neurofibroma", "heart neurofibroma", "Cardiac neurofibroma", "Cardiac Neurofibroma", "neurofibroma of heart", "Neurofibroma of Heart", "neurofibroma of the heart", "Neurofibroma of the Heart"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurofibroma of the heart", "shortest_name_length": 18}
{"curie": "MONDO:0017589", "names": ["follicular pancreatocholangitis", "follicular cholangitis and pancreatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "follicular cholangitis and pancreatitis", "shortest_name_length": 31}
{"curie": "UMLS:C5420296", "names": ["Testicular Epithelioid Mesothelioma", "Paratesticular Epithelioid Mesothelioma", "Tunica Vaginalis Epithelioid Mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paratesticular Epithelioid Mesothelioma", "shortest_name_length": 35}
{"curie": "MONDO:0007367", "names": ["FEB1", "Seizures, Familial, 1", "febrile convulsion familial", "familial febrile seizures 1", "Familial febrile convulsions", "FEBRILE SEIZURES, FAMILIAL, 1", "febrile seizures, familial, 1", "convulsions, familial febrile", "familial febrile convulsions 1", "convulsions, familial febrile, 1", "CONVULSIONS, FAMILIAL FEBRILE, 1", "Febrile Convulsions, Familial, 1", "Convulsions, Familial Febrile, 1", "Familial febrile convulsions (disorder)", "Familial febrile convulsions (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "febrile seizures, familial, 1", "shortest_name_length": 4}
{"curie": "UMLS:C1514225", "names": ["Poorly Differentiated", "Poorly Differentiated Neuroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Poorly Differentiated Neuroblastoma", "shortest_name_length": 21}
{"curie": "MONDO:0008826", "names": ["Johnston-Aarons-Schelley syndrome", "Johnston Aarons Schelley syndrome", "Arthrogryposis with Hyperkeratosis", "ARTHROGRYPOSIS WITH HYPERKERATOSIS", "arthrogryposis with hyperkeratosis", "Arthrogryposis hyperkeratosis syndrome lethal form", "Arthrogryposis-hyperkeratosis syndrome, lethal form", "arthrogryposis-hyperkeratosis syndrome, lethal form", "Arthrogryposis hyperkeratosis syndrome lethal form (disorder)", "Joint contractures, hyperkeratosis, and severe hypoplasia of the posterior columns"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthrogryposis-hyperkeratosis syndrome, lethal form", "shortest_name_length": 33}
{"curie": "MONDO:0004646", "names": ["BEDSORE", "Bedsore", "bedsore", "Bed sore", "bed sore", "Bedsores", "Bed Sore", "Decubiti", "decubitus", "Bed sores", "bed sores", "Decubitus", "Bed Sores", "Sore, Bed", "Sores, Bed", "Pressure sore", "contact ulcer", "pressure sore", "Pressure;sore", "Contact ulcer", "Pressure Sore", "Pressure ulcer", "sore; pressure", "pressure ulcer", "pressure sores", "pressure; sore", "contact ulcers", "Pressure Ulcer", "Pressure Sores", "Sore, Pressure", "Decubitus ulcer", "Ulcer;decubitus", "Pressure injury", "Decubitus Ulcer", "Ulcer, Pressure", "Sores, Pressure", "pressure injury", "decubitus ulcer", "ulcer; pressure", "Pressure Ulcers", "Pressure ulcers", "pressure ulcers", "pressure; ulcer", "DECUBITUS ULCER", "Ulcer, Decubitus", "decubitus ulcers", "Decubitus Ulcers", "Decubitus ulcers", "Ulcers, Pressure", "Pressure sore(s)", "decubitus; ulcer", "ulcer; decubitus", "Ulcers, Decubitus", "sore; pressure sore", "pressure sore; sore", "DECUBITUS SKIN ULCER", "ulcer; pressure ulcer", "pressure ulcer; ulcer", "decubitus skin ulcers", "ulcer; skin, decubitus", "decubitus ulcer, elbow", "skin; ulcer, decubitus", "Pressure Sore Or Ulcer", "DECUBITUS ULCER CHRONIC", "Skin Decubitus Ulcer(s)", "Decubitus pressure sore", "decubitus ulcer any site", "Decubitus ulcer any site", "Decubitus ulcer (specify)", "Pressure injury (disorder)", "decubitus (pressure) ulcer", "Decubitus (pressure) ulcer", "pressure injury (diagnosis)", "decubitus ulcer, lower back", "decubitus ulcer, other site", "decubitus ulcer, upper back", "Pressure ulcer, unspecified site", "Decubitus ulcer, unspecified site", "Pressure ulcer of unspecified site", "Pressure injury (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "decubitus ulcer", "shortest_name_length": 7}
{"curie": "UMLS:C5419527", "names": ["Unresectable Ovarian Undifferentiated Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Ovarian Undifferentiated Carcinoma", "shortest_name_length": 47}
{"curie": "UMLS:C1510432", "names": ["RADIATION TOXICITY", "Radiation sickness", "Radiation Sickness", "radiation toxicity", "Radiation Toxicity", "toxicity radiation", "radiation sickness", "toxicity, radiation", "Sickness, Radiation", "Radiation Sicknesses", "Sicknesses, Radiation", "Radiation sickness, NOS", "Radiation-induced vomiting", "Radiotherapy induced vomiting", "Radiation sickness (disorder)", "radiation sickness (diagnosis)", "radiation toxicity (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radiation Sickness", "shortest_name_length": 18}
{"curie": "UMLS:C3897508", "names": ["Stage IVC Oropharyngeal Lymphoepithelioma", "Stage IVC Oropharyngeal Lymphoepithelioma AJCC v7", "Stage IVC Oropharyngeal Undifferentiated Carcinoma", "Stage IVC Undifferentiated Oropharyngeal Throat Cancer", "Stage IVC Oropharyngeal Undifferentiated Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Oropharyngeal Undifferentiated Carcinoma AJCC v7", "shortest_name_length": 41}
{"curie": "UMLS:C0563269", "names": ["Acute infective exacerbation of chronic obstructive airways disease", "acute infective exacerbation of chronic obstructive airways disease", "Acute infective exacerbation of chronic obstructive airways disease (disorder)", "acute infective exacerbation of chronic obstructive airways disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute infective exacerbation of chronic obstructive airways disease", "shortest_name_length": 67}
{"curie": "UMLS:C0280419", "names": ["Recurrent Sinonasal Squamous Cell Carcinoma", "Recurrent Nasal Cavity and Paranasal Sinus Squamous Cell Cancer", "Recurrent Nasal Cavity and Paranasal Sinus Squamous Cell Carcinoma", "paranasal sinus and nasal cavity squamous cell carcinoma, recurrent", "nasal cavity and paranasal sinus squamous cell carcinoma, recurrent", "epidermoid carcinoma of the paranasal sinus and nasal cavity, recurrent", "recurrent squamous cell carcinoma of the paranasal sinus and nasal cavity", "squamous cell carcinoma of the paranasal sinus and nasal cavity, recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Sinonasal Squamous Cell Carcinoma", "shortest_name_length": 43}
{"curie": "MONDO:0032572", "names": ["CAFDADD", "TRAF7 Syndrome", "CARDIAC, FACIAL, AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY", "cardiac, facial, and digital anomalies with developmental delay", "Cardiac, Facial, and Digital Anomalies with Developmental Delay"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiac, facial, and digital anomalies with developmental delay", "shortest_name_length": 7}
{"curie": "UMLS:C0274418", "names": ["Peritoneal dialysis complication", "Complication of peritoneal dialysis", "Complication of peritoneal dialysis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Complication of peritoneal dialysis", "shortest_name_length": 32}
{"curie": "UMLS:C5239073", "names": ["Advanced Angiosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Angiosarcoma", "shortest_name_length": 21}
{"curie": "MONDO:0000702", "names": ["microscopic colitis", "colitis microscopic", "Colitis microscopic", "Microscopic Colitis", "Microscopic colitis", "Colitis, Microscopic", "Ileocolitis collagenous", "Microscopic colitis (disorder)", "microscopic colitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microscopic colitis", "shortest_name_length": 19}
{"curie": "MONDO:0100000", "names": ["MED12-related intellectual disability syndrome", "MED12 X-linked syndromic intellectual disability", "X-linked syndromic intellectual disability caused by mutation in MED12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "MED12-related intellectual disability syndrome", "shortest_name_length": 46}
{"curie": "UMLS:C0852920", "names": ["Colitis aggravated", "Aggravated Colitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colitis aggravated", "shortest_name_length": 18}
{"curie": "MONDO:0003077", "names": ["Intraocular Retinoblastoma", "intraocular retinoblastoma", "Intraocular retinoblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intraocular retinoblastoma", "shortest_name_length": 26}
{"curie": "MONDO:0003303", "names": ["Gallbladder Neurofibroma", "gallbladder neurofibroma", "gall bladder neurofibroma", "Neurofibroma of Gallbladder", "neurofibroma of gallbladder", "neurofibroma of gall bladder", "Neurofibroma of the Gallbladder", "Neurofibroma of the gallbladder", "neurofibroma of the gallbladder", "benign neurofibroma of gallbladder", "benign neurofibroma of gallbladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurofibroma of gallbladder", "shortest_name_length": 24}
{"curie": "EFO:0010178", "names": ["non-lobar intracerebral hemorrhage\"@e"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-lobar intracerebral hemorrhage\"@e", "shortest_name_length": 37}
{"curie": "UMLS:C0027659", "names": ["Experimental Tumor", "Experimental Neoplasm", "Experimental Neoplasms", "Neoplasm, Experimental", "Neoplasms, Experimental"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neoplasms, Experimental", "shortest_name_length": 18}
{"curie": "UMLS:C1334798", "names": ["Monomorphic PTLD", "PTLD (Monoclonal)", "Monomorphic Post-Transplant Lymphoproliferative Disorder", "Post-transplant lymphoproliferative disorder (Monoclonal), NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Monomorphic Post-Transplant Lymphoproliferative Disorder", "shortest_name_length": 16}
{"curie": "MONDO:0007097", "names": ["CDL2", "LCD2", "Amyloidosis 5", "amyloidosis 5", "Amyloidosis V", "amyloidosis V", "AMYLOIDOSIS V", "AGel amyloidosis", "Meretoja syndrome", "meretoja syndrome", "Meretoja's syndrome", "Gelsolin amyloidosis", "gelsolin amyloidosis", "Finnish type amyloidosis", "Meretoja type amyloidosis", "amyloidosis, Finnish type", "AMYLOIDOSIS, FINNISH TYPE", "Amyloidosis, Finnish Type", "meretoja type amyloidosis", "Amyloidosis, Meretoja Type", "amyloidosis, Meretoja type", "amyloidosis, MERETOJA type", "AMYLOIDOSIS, MERETOJA TYPE", "Hereditary gelsolin amyloidosis", "hereditary gelsolin amyloidosis", "lattice corneal dystrophy, type 2", "Familial amyloidosis Finnish type", "Lattice corneal dystrophy type II", "corneal dystrophy, lattice type 2", "LATTICE CORNEAL DYSTROPHY, TYPE II", "amyloidosis due to mutant gelsolin", "lattice corneal dystrophy, type II", "Familial amyloidosis, Finnish type", "familial amyloidosis, Finnish type", "Amyloidosis due to mutant gelsolin", "AMYLOIDOSIS DUE TO MUTANT GELSOLIN", "CORNEAL DYSTROPHY, LATTICE TYPE II", "Hereditary amyloidosis Finnish type", "AMYLOIDOSIS, FAMILIAL, FINNISH TYPE", "hereditary amyloidosis, Finnish type", "Hereditary amyloidosis, Finnish type", "Familial amyloid polyneuropathy type IV", "Type IV Familial Amyloid Polyneuropathy", "familial amyloid polyneuropathy type IV", "cerebral amyloid angiopathy, Gsn-related", "Familial Amyloid Polyneuropathy, Type IV", "CEREBRAL AMYLOID ANGIOPATHY, GSN-RELATED", "Cerebral Amyloid Angiopathy, Gsn-Related", "lattice corneal dystrophy type II Finnish", "Hereditary gelsolin amyloidosis (disorder)", "lattice corneal dystrophy, type II (diagnosis)", "amyloid cranial neuropathy with lattice corneal dystrophy", "AMYLOID CRANIAL NEUROPATHY WITH LATTICE CORNEAL DYSTROPHY", "Amyloid cranial neuropathy with lattice corneal dystrophy", "Lattice dystrophy of the cornea with hereditary generalized amyloidosis", "Lattice corneal dystrophy associated with familial systemic amyloidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Finnish type amyloidosis", "shortest_name_length": 4}
{"curie": "MONDO:0019702", "names": ["Neonatal osteosclerotic dysplasia", "neonatal osteosclerotic dysplasia", "Neonatal osteosclerotic dysplasia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal osteosclerotic dysplasia", "shortest_name_length": 33}
{"curie": "UMLS:C4289590", "names": ["Auto-Infection", "Endogenous Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endogenous Infection", "shortest_name_length": 14}
{"curie": "MONDO:0006609", "names": ["Scurf", "Dandruff", "dandruff", "DANDRUFF", "cradle cap", "Furfuracea", "SCALP SEBORRHEA", "Seborrhea sicca", "seborrhea sicca", "scalp seborrhea", "Seborrhoea sicca", "sicca; seborrhea", "seborrhea; sicca", "Pityriasis sicca", "Seborrhea capitis", "seborrhea capitis", "capitis; seborrhea", "Pityriasis capitis", "pityriasis capitis", "seborrhea; capitis", "Seborrhoea capitis", "complement 5 dysfunction", "Complement 5 dysfunction", "Seborrheic eczema of scalp", "Seborrhea sicca (disorder)", "Seborrhoeic eczema of scalp", "seborrhea capitis (diagnosis)", "Seborrheic dermatitis (scalp)", "Seborrheic dermatitis capitis", "Pityriasis capitis (disorder)", "pityriasis capitis (diagnosis)", "seborrheic dermatitis of scalp", "Seborrheic dermatitis of scalp", "Seborrhoeic dermatitis capitis", "Infantile seborrheic dermatitis", "Seborrhoeic dermatitis of scalp", "seborrheic infantile dermatitis", "infantile seborrheic dermatitis", "infantile seborrhoeic dermatitis", "Infantile seborrhoeic dermatitis", "scalp seborrheic dermatitis (disease)", "seborrheic dermatitis (disease) of scalp", "Seborrheic dermatitis of scalp (disorder)", "seborrheic dermatitis of scalp (diagnosis)", "Generalized seborrheic dermatitis of infants", "generalized seborrheic dermatitis of infants"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "seborrheic infantile dermatitis", "shortest_name_length": 5}
{"curie": "MONDO:0016192", "names": ["qualitative or quantitative defects of telethonin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of telethonin", "shortest_name_length": 49}
{"curie": "UMLS:C0029226", "names": ["organic hallucinosis", "Organic hallucinosis", "HALLUCINOSIS ORGANIC", "Organic Hallucination", "hallucinosis; organic", "Hallucination, Organic", "hallucination; organic", "Organic Hallucinations", "ORGANIC HALLUCINATIONS", "organic hallucinations", "Hallucinations, Organic", "Organic hallucinosis, NOS", "Organic hallucinosis syndrome", "organic hallucinosis syndrome", "Organic hallucinosis (disorder)", "Organic hallucinosis (diagnosis)", "organic; hallucinosis (nonalcoholic)", "Organic hallucinatory state (nonalcoholic)", "organic; hallucinatory state (nonalcoholic)", "state; organic, hallucinatory (nonalcoholic)", "organic mental disorder of unknown etiology hallucinosis", "Transient organic psychotic condition, hallucinatory type", "Psychotic disorder with hallucinations in conditions classified elsewhere"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hallucinations, Organic", "shortest_name_length": 20}
{"curie": "MONDO:0000548", "names": ["ovarian clear cell cancer", "ovarian clear cell carcinoma", "clear-cell ovarian carcinoma", "Malignant tumor, clear cell type", "malignant ovarian clear cell tumor", "Malignant Ovarian Clear Cell Tumor", "Malignant Ovarian Clear Cell Neoplasm", "malignant ovarian clear cell neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian clear cell cancer", "shortest_name_length": 25}
{"curie": "UMLS:C0153876", "names": ["ALL in Remission", "Acute lymphoid leukemia in remission", "Acute Lymphoid Leukemia in Remission", "Acute lymphoid leukaemia in remission", "Acute lymphoid leukemia, in remission", "Acute Lymphocytic Leukemia in Remission", "acute lymphocytic leukemia in remission", "Acute Lymphogenous Leukemia in Remission", "Acute Lymphocytic Leukemia (in Remission)", "Acute Lymphoblastic Leukemia in Remission", "Acute lymphocytic leukemia (in remission)", "Acute lymphocytic leukaemia (in remission)", "Acute lymphoblastic leukemia, in remission", "Acute lymphoblastic leukaemia, in remission", "acute lymphocytic leukemia (ALL) in remission", "Precursor Lymphoblastic Leukemia in Remission", "Acute lymphoid leukemia in remission (disorder)", "acute lymphocytic leukemia in remission (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute lymphoid leukemia in remission", "shortest_name_length": 16}
{"curie": "MONDO:0035669", "names": ["ADEM with anti-MOG antibodies", "acute disseminated encephalomyelitis with anti-MOG antibodies", "Acute disseminated encephalomyelitis with anti-myelin oligodendrocyte glycoprotein antibodies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute disseminated encephalomyelitis with anti-MOG antibodies", "shortest_name_length": 29}
{"curie": "MONDO:0022851", "names": ["Dennis-Fairhurst-Moore syndrome", "Dennis Fairhurst Moore syndrome", "Hallermam Streiff like syndrome", "Hallermann Streiff like syndrome", "Hallermann-Streiff-like syndrome", "Hallermann Streiff like syndrome (disorder)", "Severe Hallermann-Streiff-François syndrome", "Hallermann Streiff François syndrome severe form", "Hallermann-Streiff-François syndrome, severe form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dennis-Fairhurst-Moore syndrome", "shortest_name_length": 31}
{"curie": "MONDO:0044776", "names": ["POF10", "Pof10", "MENOQ3", "PREMATURE OVARIAN FAILURE 10", "premature ovarian failure 10", "primary ovarian insufficiency 10", "MENOPAUSE, NATURAL, AGE AT, QUANTITATIVE TRAIT LOCUS 3", "menopause, natural, Age At, quantitative trait locus 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "premature ovarian failure 10", "shortest_name_length": 5}
{"curie": "MONDO:0007425", "names": ["deafness, sensorineural, with peripheral neuropathy and arterial disease", "DEAFNESS, SENSORINEURAL, WITH PERIPHERAL NEUROPATHY AND ARTERIAL DISEASE", "Deafness, Sensorineural, with Peripheral Neuropathy and Arterial Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness, sensorineural, with peripheral neuropathy and arterial disease", "shortest_name_length": 72}
{"curie": "UMLS:C0268707", "names": ["ENCEPHALOPATHY UREMIC", "uremic encephalopathy", "Uremic encephalopathy", "Uraemic encephalopathy", "Uremic encephalopathy syndrome", "Uremic encephalopathy (disorder)", "uremic encephalopathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uremic encephalopathy", "shortest_name_length": 21}
{"curie": "MONDO:0015359", "names": ["AD demyelinating HMSN", "autosomal dominant hereditary demyelinating motor and sensory neuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant hereditary demyelinating motor and sensory neuropathy", "shortest_name_length": 21}
{"curie": "MONDO:0001721", "names": ["ISD", "Intrinsic sphincter deficiency", "intrinsic sphincter deficiency", "Intrinsic sphincter deficiency (ISD)", "Urethral intrinsic sphincter deficiency", "intrinsic urethral sphincter deficiency", "Intrinsic urethral sphincter deficiency", "urethral intrinsic sphincter deficiency", "intrinsic sphincter deficiency (diagnosis)", "Intrinsic (urethral) sphincter deficiency [ISD]", "intrinsic (urethral) sphincter deficiency [ISD]", "Urethral intrinsic sphincter deficiency (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "urethral intrinsic sphincter deficiency", "shortest_name_length": 3}
{"curie": "MONDO:0024315", "names": ["Parasitic Endophthalmitis", "parasitic endophthalmitis", "Parasitic endophthalmitis", "parasitic; endophthalmitis", "endophthalmitis; parasitic", "Endophthalmitis, parasitic", "Parasitic endophthalmitis NOS", "Parasitic endophthalmitis, NOS", "Parasitic endophthalmitis (disorder)", "parasitic endophthalmitis (diagnosis)", "Parasitic endophthalmitis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parasitic endophthalmitis", "shortest_name_length": 25}
{"curie": "MONDO:0044617", "names": ["X-linked keloid scarring-reduced joint mobility-increased optic cup-to-disc ratio syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked keloid scarring-reduced joint mobility-increased optic cup-to-disc ratio syndrome", "shortest_name_length": 90}
{"curie": "MONDO:0012484", "names": ["Face blindness", "face blindness", "congenital prosopagnosia", "hereditary prosopagnosia", "Prosopagnosia, congenital", "PROSOPAGNOSIA, HEREDITARY", "PROSOPAGNOSIA, CONGENITAL", "prosopagnosia, congenital", "prosopagnosia, hereditary", "Prosopagnosia, hereditary", "developmental prosopagnosia", "Developmental Prosopagnosia", "Prosopagnosia, Developmental", "prosopagnosia, developmental", "Developmental Prosopagnosias", "PROSOPAGNOSIA, DEVELOPMENTAL", "Prosopagnosias, Developmental", "hereditary prosopagnosia (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prosopagnosia, hereditary", "shortest_name_length": 14}
{"curie": "UMLS:C0160422", "names": ["kidney injury closed", "Closed injury of kidney", "Closed injury of kidney (disorder)", "Closed injury of kidney (diagnosis)", "Injury to kidney without mention of open wound into cavity", "Injury to Kidney without mention of Open Wound into Cavity", "Unspecified injury to kidney without mention of open wound into cavity", "Injury to kidney without mention of open wound into cavity, unspecified injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Closed injury of kidney", "shortest_name_length": 20}
{"curie": "MONDO:0001800", "names": ["Equatorial staphyloma", "equatorial staphyloma", "Equatorial scleral staphyloma", "Equatorial staphyloma (disorder)", "equatorial staphyloma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "equatorial staphyloma", "shortest_name_length": 21}
{"curie": "UMLS:C1096715", "names": ["Metastatic Testicular Cancer", "Testicular cancer metastatic", "Metastatic Malignant Testicular Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular cancer metastatic", "shortest_name_length": 28}
{"curie": "MONDO:0008807", "names": ["CSA", "Central Apnea", "Apnea, Central", "Central Apneas", "Apneas, Central", "Ondine Syndrome", "ondine syndrome", "Central Sleep Apnea", "apnea central sleep", "central sleep apnea", "Central sleep apnea", "sleep apnea central", "apnea, central sleep", "Sleep Apnea, Central", "Central sleep apnoea", "Central Sleep Apneas", "Apnea, Central Sleep", "APNEA, CENTRAL SLEEP", "central sleep apnoea", "Sleep Apneas, Central", "Apneas, Central Sleep", "Apnea, Sleep, Central", "CSA - Central sleep apnea", "CSA - Central sleep apnoea", "Sleep Apnea, Lethal Central", "SLEEP APNEA, LETHAL CENTRAL", "sleep apnea, lethal central", "Central Sleep Apnea Syndrome", "central sleep apnea (diagnosis)", "central alveolar hypoventilation", "Central Alveolar Hypoventilation", "Alveolar Hypoventilation, Central", "Hypoventilation, Central Alveolar", "Hypoventilations, Central Alveolar", "Alveolar Hypoventilations, Central", "Central Sleep Disordered Breathing", "Central Sleep-Disordered Breathing", "Sleep Disordered Breathing, Central", "Sleep-Disordered Breathing, Central", "Central Sleep-Disordered Breathings", "Breathing, Central Sleep-Disordered", "Sleep-Disordered Breathings, Central", "Breathings, Central Sleep-Disordered", "Central Alveolar Hypoventilation Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "apnea, central sleep", "shortest_name_length": 3}
{"curie": "MONDO:0000210", "names": ["thiopurine metabolic disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thiopurine metabolic disease", "shortest_name_length": 28}
{"curie": "UMLS:C0016508", "names": ["anomaly; foot", "foot; anomaly", "Foot anomalies", "pes; deformity", "deformity; pes", "feet deformities", "Malformation foot", "foot malformation", "MALFORMATION FOOT", "Malformation foot NOS", "Congenital Foot Deformity", "congenital foot deformity", "anomalies congenital foot", "Deformity;foot;congenital", "Deformity, Congenital Foot", "Foot Deformity, Congenital", "Congenital Foot Deformities", "deformity; foot, congenital", "congenital foot deformities", "Foot Deformities, Congenital", "Congenital deformity of foot", "Congenital foot malformation", "congenital deformity of foot", "Deformities, Congenital Foot", "Congenital deformities of feet", "Congenital anomaly of foot, NOS", "Congenital deformity of foot NOS", "Congenital foot malformation NOS", "Congenital deformity of foot, NOS", "Congenital deformity of foot (disorder)", "congenital deformity of foot (diagnosis)", "Congenital deformity of feet, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital Foot Deformity", "shortest_name_length": 13}
{"curie": "UMLS:C0343387", "names": ["Ileocecal Syndrome", "Neutropenic enterocolitis", "Neutropenic Enterocolitis", "Enterocolitis, Neutropenic", "Neutropaenic enterocolitis", "Neutropaenic enterocolitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Enterocolitis, Neutropenic", "shortest_name_length": 18}
{"curie": "UMLS:C3897732", "names": ["Recurrent Pancreatic Neuroendocrine Cancer", "Recurrent Pancreatic Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Pancreatic Neuroendocrine Carcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0005059", "names": ["LEUKEMIA", "Leukemia", "leukemia", "Leukemias", "Leukaemia", "LEUKAEMIA", "leukaemia", "LEUKEMIAS", "leukemias", "Leukaemias", "leukaemias", "Leukemia NOS", "Blood cancer", "Leukaemia NOS", "type leukemia", "Leukemia, NOS", "Leucocythemia", "leukemia type", "Leucocythaemia", "Leucocythemias", "LEUKEMIAS, NOS", "leukemia types", "Leukaemia, NOS", "types leukemia", "leukemias types", "Leucocythaemias", "blood (leukemia)", "Blood (Leukemia)", "Leukemia, disease", "Leukemia, Disease", "leukemia, disease", "Leukaemia, disease", "leukemias, general", "Leukemias, General", "leukemia (disease)", "LEUKEMIA, MALIGNANT", "leukemia, malignant", "Leukemia morphology", "Unspecified leukemia", "Leukemia unspecified", "Leukaemia morphology", "leukemia (diagnosis)", "Unspecified Leukemias", "Leukemia, unspecified", "Unspecified leukaemia", "all types of leukemia", "Leukaemia unspecified", "Leukaemia, unspecified", "Leukemia, disease (disorder)", "Leukemia of unspecified cell type", "Leukaemia of unspecified cell type", "Leukemia (morphologic abnormality)", "Leukemia, NOS, without mention of remission", "Leukaemia, NOS, without mention of remission", "Unspecified leukemia without mention of remission", "Unspecified leukaemia without mention of remission", "Leukemia, unspecified, without mention of remission", "Leukaemia, unspecified, without mention of remission"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukemia", "shortest_name_length": 8}
{"curie": "UMLS:C5446560", "names": ["Lacrimal Sac Lymphoma", "Primary Lacrimal Sac Lymphoma", "Lacrimal Sac Non-Hodgkin Lymphoma", "Lacrimal Drainage System Lymphoma", "Primary Lacrimal Sac Non-Hodgkin Lymphoma", "Primary Lacrimal Drainage System Lymphoma", "Lacrimal Drainage System Non-Hodgkin Lymphoma", "Primary Lacrimal Drainage System Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lacrimal Drainage System Non-Hodgkin Lymphoma", "shortest_name_length": 21}
{"curie": "MONDO:0006174", "names": ["Cortisol-Producing Adrenal Gland Adenoma", "Cortisol Producing Adrenal Cortex Adenoma", "Cortisol-Producing Adrenal Cortex Adenoma", "cortisol-producing adrenal cortex adenoma", "cortisol producing adrenal cortex adenoma", "Cortisol Producing Adrenal Cortical Adenoma", "cortisol producing adrenal cortical adenoma", "Cortisol-Producing Adrenal Cortical Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cortisol-producing adrenal cortex adenoma", "shortest_name_length": 40}
{"curie": "UMLS:C1333271", "names": ["Deletion of Short Arm of Chromosome 1 (1p) Associated Meningioma", "Deletion of the Short Arm of Chromosome 1 (1p) Associated Meningioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Deletion of the Short Arm of Chromosome 1 (1p) Associated Meningioma", "shortest_name_length": 64}
{"curie": "MONDO:0700017", "names": ["chromosome 10 disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 10 disorder", "shortest_name_length": 22}
{"curie": "MONDO:0013105", "names": ["BCC5", "BASAL CELL CARCINOMA, SUSCEPTIBILITY TO, 5", "basal cell carcinoma, susceptibility to, 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "basal cell carcinoma, susceptibility to, 5", "shortest_name_length": 4}
{"curie": "MONDO:0001544", "names": ["nerve palsy tibial", "tibial nerve palsy", "Tibial nerve palsy", "medial popliteal nerve palsy", "nerve palsy medial popliteal", "Tibial nerve palsy (disorder)", "tibial nerve palsy (diagnosis)", "medial popliteal nerve palsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tibial nerve palsy", "shortest_name_length": 18}
{"curie": "UMLS:C2981410", "names": ["Stage IB Gastric Gastrointestinal Stromal Tumor", "Stage IB Gastric Gastrointestinal Stromal Tumor AJCC v7", "Stage IB Gastric (Stomach) Gastrointestinal Stromal Tumor (GIST)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Gastric Gastrointestinal Stromal Tumor", "shortest_name_length": 47}
{"curie": "MONDO:0010410", "names": ["AGA2", "ALOPECIA, ANDROGENETIC, 2", "Alopecia, Androgenetic, 2", "alopecia, androgenetic, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alopecia, androgenetic, 2", "shortest_name_length": 4}
{"curie": "MONDO:0023093", "names": ["exertional headache", "primary Exertional headache", "primary headache associated with sexual activity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exertional headache", "shortest_name_length": 19}
{"curie": "MONDO:0010171", "names": ["USH1C", "Usher syndrome type IC", "Usher syndrome type 1C", "USHER SYNDROME, TYPE IC", "Usher syndrome, type 1C", "USHER syndrome, type IC", "Usher Syndrome, Type IC", "Usher syndrome, Acadian variety", "Usher syndrome type I Acadian variety", "Usher syndrome, type I, Acadian variety", "USHER SYNDROME, TYPE I, ACADIAN VARIETY", "Usher Syndrome, Type I, Acadian Variety"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Usher syndrome type 1C", "shortest_name_length": 5}
{"curie": "MONDO:0002345", "names": ["cervicitis", "Cervicitis", "CERVICITIS", "Trachelitis", "TRACHELITIS", "trachelitis", "Cervicitides", "Cervicitis NOS", "Cervicitis, NOS", "Uterine cervicitis", "cellulitis; cervix", "cervix; cellulitis", "Uterine Cervicitis", "Cervix inflammation", "Cervicitis, Uterine", "cervix inflammation", "inflammation cervix", "Uterine Cervicitides", "cervicitis (disease)", "inflammation; cervix", "cervix; inflammation", "endocervix; infection", "infection; endocervix", "Cervicitides, Uterine", "cervicitis (diagnosis)", "inflammation of cervix", "Inflammation of cervix", "Uterine cervix inflammation", "UTERINE CERVIX, INFLAMMATION", "cervix; disease, inflammatory", "cervicitis and endocervicitis", "Cervicitis and endocervicitis", "Inflammation of cervix (disorder)", "Inflammatory disease of the cervix", "Inflammatory disease of cervix uteri", "inflammatory disease of cervix uteri", "Uterine cervicitis and endocervicitis", "Cervicitis and endocervicitis (disorder)", "cervicitis and endocervicitis (diagnosis)", "Inflammatory disease of the uterine cervix", "inflammatory disease of cervix uteri (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervicitis", "shortest_name_length": 10}
{"curie": "UMLS:C0334434", "names": ["Melanoma in Junctional Nevus", "Malignant Melanoma in Junctional Nevus", "Malignant melanoma in junctional nevus", "Malignant melanoma in junctional naevus", "Malignant Skin Melanoma in Junctional Nevus", "Cutaneous (Skin) Melanoma in Junctional Nevus", "malignant melanoma of skin in junctional nevus", "Malignant Melanoma of Skin in Junctional Nevus", "Malignant Melanoma of the Skin in Junctional Nevus", "malignant melanoma of skin in junctional nevus (diagnosis)", "Malignant melanoma in junctional nevus (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant melanoma in junctional nevus", "shortest_name_length": 28}
{"curie": "MONDO:0014743", "names": ["RCDP5", "Rcdp5", "PEX5 rhizomelic chondrodysplasia punctata", "Rhizomelic chondrodysplasia punctata type 5", "rhizomelic chondrodysplasia punctata type 5", "RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 5", "rhizomelic chondrodysplasia punctata, type 5", "rhizomelic chondrodysplasia punctata caused by mutation in PEX5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rhizomelic chondrodysplasia punctata type 5", "shortest_name_length": 5}
{"curie": "MONDO:0007365", "names": ["BFNS1", "myokymia", "seizures, benign neonatal, 1", "KCNQ2 benign neonatal seizures", "seizures, benign familial neonatal, 1", "SEIZURES, BENIGN FAMILIAL NEONATAL, 1", "seizures, benign familial neonatal, type 1", "epilepsy, benign neonatal, 1, and/or myokymia", "Epilepsy, Benign Neonatal, 1, And-Or Myokymia", "EPILEPSY, BENIGN NEONATAL, 1, AND/OR MYOKYMIA", "benign neonatal seizures caused by mutation in KCNQ2", "SEIZURES, BENIGN FAMILIAL NEONATAL, 1, AND/OR MYOKYMIA", "seizures, benign familial neonatal, 1, and/or myokymia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "seizures, benign familial neonatal, 1", "shortest_name_length": 5}
{"curie": "UMLS:C1336120", "names": ["Stage IA Osteosarcoma", "Stage IA Osteogenic Sarcoma", "Stage IA Osteosarcoma AJCC v7", "Stage IA Osteosarcoma  AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA Osteosarcoma AJCC v7", "shortest_name_length": 21}
{"curie": "MONDO:0001465", "names": ["Superficial keratitis", "Keratitis superficial", "superficial keratitis", "keratitis; superficial", "superficial; keratitis", "Superficial keratitis, NOS", "Superficial keratitis (disorder)", "superficial keratitis (diagnosis)", "Unspecified superficial keratitis", "Superficial keratitis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "superficial keratitis", "shortest_name_length": 21}
{"curie": "UMLS:C4303663", "names": ["Extensive stage primary small cell carcinoma of lung", "Extensive stage primary small cell carcinoma of lung (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Extensive stage primary small cell carcinoma of lung", "shortest_name_length": 52}
{"curie": "MONDO:0002817", "names": ["adrenal tumor", "Adrenal tumor", "ADRENAL TUMOR", "Adrenal Tumor", "Adrenal Cancer", "Adrenal tumour", "adrenal cancer", "cancer adrenal", "adrenal tumors", "adrenal tumour", "adrenals cancer", "adrenal tumours", "Adrenal Cancers", "Cancer, Adrenal", "ADRENAL NEOPLASM", "NEOPLASM ADRENAL", "Adrenal Neoplasm", "adrenal neoplasm", "Cancers, Adrenal", "Neoplasm adrenal", "Adrenal neoplasm", "adrenal neoplasms", "Adrenal neoplasms", "Adrenal Neoplasms", "Adrenal neoplasia", "Neoplasm, Adrenal", "Neoplasms, Adrenal", "tumor adrenal gland", "Adrenal Gland Tumor", "adrenal gland tumor", "adrenal gland tumors", "Adrenal Gland Cancer", "Adrenal neoplasm NOS", "adrenal gland cancer", "adrenal gland tumour", "adrenal cancer gland", "Adrenal gland cancer", "adrenal glands tumor", "cancer adrenal gland", "adrenal gland tumours", "Adrenal Gland Cancers", "adrenal glands tumors", "Cancer, Adrenal Gland", "adrenal cancer glands", "Tumor of adrenal gland", "Tumor of Adrenal Gland", "tumor of adrenal gland", "Cancers, Adrenal Gland", "Adrenal glands--Cancer", "Adrenal glands--Tumors", "adrenal gland neoplasm", "Adrenal Gland Neoplasm", "cancer of adrenal gland", "Adrenal Gland Neoplasms", "Neoplasm, Adrenal Gland", "adrenal gland neoplasms", "Tumour of adrenal gland", "Cancer of adrenal gland", "Malignant Adrenal Tumor", "malignant Adrenal tumor", "malignant adrenal tumor", "Neoplasms, Adrenal Gland", "Adrenal gland malignancy", "neoplasm of adrenal gland", "Neoplasm of Adrenal Gland", "Neoplasm of adrenal gland", "tumor of the adrenal gland", "malignant adrenal neoplasm", "tumor of the Adrenal gland", "Tumor of the Adrenal Gland", "Malignant Adrenal Neoplasm", "Adrenal neoplasms malignant", "cancer of the adrenal gland", "Cancer of the Adrenal Gland", "CA - Cancer of adrenal gland", "malignant adrenal gland tumor", "Neoplasm of the Adrenal Gland", "Neoplasm of the adrenal gland", "Malignant Adrenal Gland Tumor", "Malignant tumor of adrenal gland", "Malignant Tumor of Adrenal Gland", "Malignant Adrenal Gland Neoplasm", "malignant tumor of adrenal gland", "malignant adrenal gland neoplasm", "Malignant tumour of adrenal gland", "Malignant Neoplasm of Adrenal Gland", "Malignant neoplasm of adrenal gland", "malignant neoplasm of adrenal gland", "Malignant Tumor of the Adrenal Gland", "malignant tumor of the adrenal gland", "Neoplasm of adrenal gland (disorder)", "neoplasm of adrenal gland (diagnosis)", "Malignant neoplasm of suprarenal gland", "Malignant Neoplasm of the Adrenal Gland", "malignant neoplasm of the adrenal gland", "Malignant tumor of adrenal gland (disorder)", "malignant neoplasm of adrenal gland (diagnosis)", "Malignant neoplasm of adrenal gland, unspecified", "Malignant neoplasm of unspecified part of adrenal gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adrenal gland cancer", "shortest_name_length": 13}
{"curie": "UMLS:C0853844", "names": ["Nodal osteoarthritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nodal osteoarthritis", "shortest_name_length": 20}
{"curie": "UMLS:C1332282", "names": ["Grade 3 Hemispheric Astrocytoma", "Grade III Hemispheric Astrocytoma", "Hemispheric Anaplastic Astrocytoma", "Anaplastic Hemispheric Astrocytoma", "Anaplastic Astrocytoma, Hemispheric", "Grade 3 Hemispheric Astrocytic Tumor", "Grade III Hemispheric Astrocytic Tumor", "Grade 3 Hemispheric Astrocytic Neoplasm", "Grade 3 Cerebral Hemisphere Astrocytoma", "Grade III Cerebral Hemisphere Astrocytoma", "Grade III Hemispheric Astrocytic Neoplasm", "Cerebral Hemisphere Anaplastic Astrocytoma", "Grade 3 Astrocytoma of Cerebral Hemisphere", "Grade III Astrocytoma of Cerebral Hemisphere", "Anaplastic Astrocytoma of Cerebral Hemisphere", "Grade III Cerebral Hemisphere Astrocytic Tumor", "Grade 3 Astrocytoma of the Cerebral Hemisphere", "Grade 3 Astrocytic Tumor of Cerebral Hemisphere", "Grade 3 Cerebral Hemisphere Astrocytic Neoplasm", "Anaplastic Astrocytoma of the Cerebral Hemisphere", "Grade III Astrocytic Tumor of Cerebral Hemisphere", "Grade III Cerebral Hemisphere Astrocytic Neoplasm", "Grade 3 Astrocytic Neoplasm of Cerebral Hemisphere", "Grade 3 Astrocytic Tumor of the Cerebral Hemisphere", "Undifferentiated Astrocytoma of Cerebral Hemisphere", "Grade III Astrocytic Neoplasm of Cerebral Hemisphere", "Grade III Astrocytic Tumor of the Cerebral Hemisphere", "Grade 3 Astrocytic Neoplasm of the Cerebral Hemisphere", "Undifferentiated Astrocytoma of the Cerebral Hemisphere", "Grade III Astrocytic Neoplasm of the Cerebral Hemisphere"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anaplastic Hemispheric Astrocytoma", "shortest_name_length": 31}
{"curie": "MONDO:0009479", "names": ["JBS", "Johanson-Blizzard Syndrome", "johanson blizzard syndrome", "Johanson-Blizzard syndrome", "johanson-blizzard syndrome", "Johanson Blizzard syndrome", "JOHANSON-BLIZZARD SYNDROME", "Johanson-BLIZZARD syndrome", "Johanson-Blizzard syndrome (JBS)", "Johanson-Blizzard syndrome (disorder)", "pancreatic insufficiency, combined exocrine", "Pancreatic Insufficiency, Combined Exocrine", "Ectodermal Dysplasia-Exocrine Pancreatic Insufficiency", "Malabsorption-Ectodermal Dysplasia-Nasal Alar Hypoplasia", "Nasal Alar Hypoplasia, Hypothyroidism, Pancreatic Achylia, Congenital Deafness", "nasal alar hypoplasia, hypothyroidism, pancreatic achylia and congenital deafness", "Nasal Alar Hypoplasia, Hypothyroidism, Pancreatic Achylia, and Congenital Deafness", "nasal alar hypoplasia, hypothyroidism, pancreatic achylia, and congenital deafness", "NASAL ALAR HYPOPLASIA, HYPOTHYROIDISM, PANCREATIC ACHYLIA, AND CONGENITAL DEAFNESS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Johanson-Blizzard syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C5421214", "names": ["Malignant Visual Pathway Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Visual Pathway Neoplasm", "shortest_name_length": 33}
{"curie": "MONDO:0015631", "names": ["VWD2N", "Von Willebrand disease type 2N", "von Willebrand disease type 2N", "Type 2N von Willebrand Disease", "von Willebrand Disease, Type 2N", "VON WILLEBRAND DISEASE, TYPE 2N", "Type IIN von Willebrand Disease", "Von Willebrand disease, type 2N", "von Willebrand disease, type 2N", "von Willebrand Disease, Type IIN", "von Willebrand disease Normandy variant", "von Willebrand Disease Normandy Variant", "Hereditary von Willebrand disease type 2N", "von Willebrand disease type 2N (diagnosis)", "Hereditary von Willebrand disease type 2N (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "von Willebrand disease type 2N", "shortest_name_length": 5}
{"curie": "MONDO:0009895", "names": ["polydactyly, postaxial, with dental and vertebral anomalies", "POLYDACTYLY, POSTAXIAL, WITH DENTAL AND VERTEBRAL ANOMALIES", "Polydactyly, Postaxial, with Dental and Vertebral Anomalies", "postaxial polydactyly-dental and vertebral anomalies syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postaxial polydactyly-dental and vertebral anomalies syndrome", "shortest_name_length": 59}
{"curie": "MONDO:0005570", "names": ["Blood Disease", "Disease;blood", "Blood disease", "blood disease", "Blood disorder", "Blood diseases", "blood; disease", "Disease, Blood", "blood diseases", "blood disorder", "Blood Diseases", "Blood Disorder", "Diseases, Blood", "Blood--Diseases", "blood dyscrasia", "blood disorders", "Blood Disorders", "BLOOD DYSCRASIA", "Blood dyscrasia", "Blood Dyscrasia", "blood dyscrasias", "dyscrasia; blood", "blood; dyscrasia", "Blood disorder NOS", "hematologic disease", "Hematologic Disease", "Hematologic disease", "HEMATOLOGIC PROBLEM", "Hemopoietic disease", "Blood dyscrasia NOS", "Blood disorder, NOS", "disease of the blood", "hematologic diseases", "Disease, Hematologic", "Hemopoietic disorder", "HEMATOLOGIC DISORDER", "hematologic disorder", "DISORDER HEMATOLOGIC", "Hematologic diseases", "Haemopoietic disease", "DISORDER BLOOD (NOS)", "Hematologic Diseases", "Haematologic disease", "Blood dyscrasia, NOS", "Hematologic Disorder", "hematologic disorders", "Hematological Disease", "blood system disorder", "Hematological disease", "Hematologic Disorders", "Haemopoietic disorder", "hematological disease", "DYSCRASIA BLOOD (NOS)", "HEMATOLOGIC DISORDERS", "Diseases, Hematologic", "hematopoietic disease", "Dyscrasia blood (NOS)", "hematological diseases", "hematological disorder", "Hematological Diseases", "Disease, Hematological", "Hematological Disorder", "Hematological disorders", "Diseases, Hematological", "Abnormal;haematological", "hematological disorders", "hematological; disorder", "blood disorder diagnosis", "Hematologic disease, NOS", "HEMATOLOGIC PROBLEM, NOS", "haematological disorders", "Haematological disorders", "rare hematologic disease", "Blood dyscrasia syndrome", "hematological abnormality", "Haematologic disease, NOS", "Hematological abnormality", "haematological abnormality", "Haematological abnormality", "hematopoietic system disease", "hematological system disease", "disease (or disorder); blood", "haematopoietic system disease", "Hematopoietic system syndrome", "Haematopoietic system syndrome", "disease of hematopoietic system", "Disorder of hematopoietic system", "disease of haematopoietic system", "disorder of hematopoietic system", "Disorder of haematopoietic system", "hematologic disorders (diagnosis)", "Hematopoietic system syndrome, NOS", "Haematopoietic system syndrome, NOS", "Hematologic and Lymphocytic Disorder", "Disease of hematopoietic system, NOS", "disease (or disorder); hematological", "hematologic and lymphocytic disorder", "Disease of haematopoietic system, NOS", "Disorder of hematopoietic system, NOS", "Disorder of haematopoietic system, NOS", "Abnormality of the hematopoietic system", "blood and blood-forming organ disorders", "Disorder of cellular component of blood", "Abnormality of the haematopoietic system", "hematological disorders and malignancies", "hematopoietic system disease or disorder", "Hematopoietic system disease or syndrome", "Diseases of blood and blood-forming organs", "Disease of blood AND/OR blood-forming organ", "disorders of blood and blood-forming organs", "disease or disorder of hematopoietic system", "Disease of blood AND/OR blood forming organ", "HEMATOPOIETIC SYSTEM DISEASES: GENERAL TERMS", "disease of the blood and blood-forming organs", "Disease of blood and blood forming organ, NOS", "DISEASE OF THE BLOOD AND BLOOD-FORMING ORGANS", "DISEASES OF THE BLOOD AND BLOOD-FORMING ORGANS", "Abnormality of blood and blood-forming tissues", "Diseases of the blood and blood-forming organs", "DISEASES OF THE HEMATOPOIETIC AND IMMUNE SYSTEMS", "Disorder of cellular component of blood (disorder)", "General Hematopoietic System Diseases and Syndromes", "Unspecified diseases of blood and blood-forming organs", "Disease of blood and blood-forming organs, unspecified", "disorders of blood and blood-forming organs (diagnosis)", "Disorder of hematopoietic system (navigational concept)", "Disease of blood AND/OR blood-forming organ (navigational concept)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hematologic disorder", "shortest_name_length": 13}
{"curie": "MONDO:0018503", "names": ["gastric carcinoma, salivary gland type", "carcinoma of stomach, salivary gland type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma of stomach, salivary gland type", "shortest_name_length": 38}
{"curie": "MONDO:0007487", "names": ["DYX4", "DYX1", "DYX7", "WORD-BLINDNESS, CONGENITAL", "Word-blindness, congenital", "susceptibility to dyslexia 1", "DYSLEXIA, SUSCEPTIBILITY TO, 7", "DYSLEXIA, SUSCEPTIBILITY TO, 1", "DYSLEXIA, SUSCEPTIBILITY TO, 4", "dyslexia, susceptibility to, 1", "dyslexia, susceptibility to, 4", "dyslexia, susceptibility to, 7", "READING DISABILITY, SPECIFIC, 1", "reading disability, specific, 1", "dyslexia, susceptibility to, type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dyslexia, susceptibility to, 1", "shortest_name_length": 4}
{"curie": "MONDO:0020110", "names": ["Apulmonism", "lung; absent", "Lung agenesis", "aplasia; lung", "lung; aplasia", "absence; lung", "lung; agenesis", "agenesis; lung", "Absence of lung", "Aplasia of lung", "Agenesis of lung", "agenesis of lung", "Pulmonary aplasia", "Pulmonary agenesis", "pulmonary agenesis", "Pulmonary Agenesis", "congenital lung agenesis", "Congenital lung agenesis", "unilateral lung agenesis", "Unilateral lung agenesis", "Congenital aplasia of lung", "Congenital Absence of Lung", "congenital absence of lung", "Congenital absence of lung", "Agenesis of lung (disorder)", "agenesis of lung (diagnosis)", "Unilateral pulmonary agenesis", "congenital anomaly of lung agenesis", "unilateral lobar pulmonary agenesis", "Congenital absence of lung (disorder)", "Congenital aplasia of lung (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary agenesis", "shortest_name_length": 10}
{"curie": "UMLS:C0746883", "names": ["fever neutropenic", "fever neutropenia", "Neutropenic fever", "neutropenia fever", "neutropenic fever", "NEUTROPENIA FEVER", "Neutropaenic fever", "febrile neutropenia", "neutropenia febrile", "Febrile Neutropenia", "Febrile neutropenia", "Neutropenia, Febrile", "Febrile Neutropenias", "Neutropenias, Febrile", "neutropenic fever (diagnosis)", "Febrile neutropenia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Febrile Neutropenia", "shortest_name_length": 17}
{"curie": "MONDO:0003695", "names": ["ovary clear cell adenofibroma", "ovarian clear cell adenofibroma", "Ovarian Clear Cell Adenofibroma", "clear cell adenofibroma of ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian clear cell adenofibroma", "shortest_name_length": 29}
{"curie": "UMLS:C4505436", "names": ["Generalized Absence Seizure", "Absence Seizure, Generalized", "Generalized Absence Seizures", "Seizure, Generalized Absence", "Absence Seizures, Generalized"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Generalized Absence Seizures", "shortest_name_length": 27}
{"curie": "MONDO:0017855", "names": ["T-B- SCID", "T-B- severe combined immunodeficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-B- severe combined immunodeficiency", "shortest_name_length": 9}
{"curie": "UMLS:C1335429", "names": ["Plasmacytoma-like PTLD", "Plasmacytoma-Like Post-Transplant Lymphoproliferative Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Plasmacytoma-Like Post-Transplant Lymphoproliferative Disorder", "shortest_name_length": 22}
{"curie": "MONDO:0008860", "names": ["BAIBA", "BAIB Urinary Excretion", "Baib urinary excretion", "BAIB URINARY EXCRETION", "beta-Aminoisobutyricaciduria", "beta Aminoisobutyricaciduria", "Beta-aminoisobutyric aciduria", "BETA-AMINOISOBUTYRIC ACIDURIA", "BETA-aminoisobutyric aciduria", "HYPER-BETA-AMINOISOBUTYRIC ACIDURIA", "Hyper-Beta-Aminoisobutyric Aciduria", "hyper-Beta-aminoisobutyric aciduria", "BAIBA - beta-aminoisobutyric aciduria", "Beta-aminoisobutyric aciduria (disorder)", "BETA-AMINOISOBUTYRIC ACID, URINARY EXCRETION OF", "Beta-Aminoisobutyric Acid, Urinary Excretion of", "beta-aminoisobutyric acid, urinary excretion of"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "beta-aminoisobutyric acid, urinary excretion of", "shortest_name_length": 5}
{"curie": "MONDO:0012729", "names": ["ECYT4", "familial erythrocytosis 4", "ERYTHROCYTOSIS, FAMILIAL, 4", "erythrocytosis, familial, 4", "Erythrocytosis, Familial, 4", "EPAS1 familial polycythemia", "erythrocytosis, familial, type 4", "familial polycythemia caused by mutation in EPAS1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythrocytosis, familial, 4", "shortest_name_length": 5}
{"curie": "UMLS:C0432361", "names": ["Diffuse neurofibroma", "Diffuse Neurofibroma", "Diffuse neurofibroma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse neurofibroma", "shortest_name_length": 20}
{"curie": "UMLS:C5206478", "names": ["Locally Advanced Unresectable Colorectal Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Unresectable Colorectal Adenocarcinoma", "shortest_name_length": 55}
{"curie": "UMLS:C4727196", "names": ["Recurrent Gastroesophageal Junction Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Gastroesophageal Junction Adenocarcinoma", "shortest_name_length": 50}
{"curie": "MONDO:0009312", "names": ["Peptide growth factors deficiency", "peptide growth factors deficiency", "Hoepffner dreyer reimers syndrome", "Hoepffner-Dreyer-Reimers syndrome", "Hoepffner Dreyer Reimers syndrome", "Growth Factors, Combined Defect of", "growth factors, combined defect OF", "Peptidic growth factors deficiency", "peptidic growth factors deficiency", "GROWTH FACTORS, COMBINED DEFECT OF", "Lipodystrophy due to peptidic growth factors deficiency", "lipodystrophy due to peptidic growth factors deficiency", "Werner-Like Syndrome due to Combined Growth Factor Deficiency", "Werner-like syndrome due to combined Growth Factor deficiency", "Werner-like syndrome due to combined growth factor deficiency", "WERNER-LIKE SYNDROME DUE TO COMBINED GROWTH FACTOR DEFICIENCY", "Lipodystrophy due to peptidic growth factors deficiency (disorder)", "INSULIN, INSULIN-LIKE GROWTH FACTOR I, AND EPIDERMAL GROWTH FACTOR DEFICIENCY", "insulin, insulin-like Growth Factor I, and Epidermal Growth Factor deficiency", "Insulin, Insulin-Like Growth Factor I, and Epidermal Growth Factor Deficiency", "Combined insulin, insulin-like growth factor 1 and epidermal growth factor deficiency", "combined insulin, insulin-like growth factor 1 (IGF1) and epidermal growth factor (EGF) deficiency", "Combined insulin, insulin-like growth factor 1 (IGF1) and epidermal growth factor (EGF) deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lipodystrophy due to peptidic growth factors deficiency", "shortest_name_length": 33}
{"curie": "UMLS:C1710164", "names": ["Sporadic Cylindroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sporadic Cylindroma", "shortest_name_length": 19}
{"curie": "UMLS:C5239499", "names": ["Refractory Thyroid Gland Oncocytic Carcinoma", "Refractory Thyroid Gland Hurthle Cell Carcinoma", "Refractory Thyroid Gland Oncocytic (Hurthle Cell) Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Thyroid Gland Oncocytic Carcinoma", "shortest_name_length": 44}
{"curie": "MONDO:0013223", "names": ["SMDMDM", "PAM16 spondylodysplastic dysplasia", "CHONDRODYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE", "Megarbane-Dagher-Melike type chondrodysplasia", "chondrodysplasia, Megarbane-Dagher-Melki type", "Chondrodysplasia, Megarbane-Dagher-Melki Type", "spondylodysplastic dysplasia caused by mutation in PAM16", "spondylometaphyseal dysplasia, MEGARBANE-DAGHER-MELKI type", "SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE", "spondylometaphyseal dysplasia Megarbane-Dagher-Melike type", "spondylometaphyseal dysplasia, Megarbane-Dagher-Melike type", "autosomal recessive spondylometaphyseal dysplasia, Mégarbané type", "autosomal recessive spondylometaphyseal dysplasia, Megarbane type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive spondylometaphyseal dysplasia, Megarbane type", "shortest_name_length": 6}
{"curie": "MONDO:0013376", "names": ["MCOPCB6", "microphthalmia with coloboma 6", "microphthalmia with coloboma 6, digenic", "MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 6", "microphthalmia, isolated, with coloboma 6", "microphthalmia, isolated, with coloboma type 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microphthalmia, isolated, with coloboma 6", "shortest_name_length": 7}
{"curie": "MONDO:0011082", "names": ["OAFNS", "OCULOAURICULOFRONTONASAL SYNDROME", "OCULOAURICULOFRONTONASAL syndrome", "oculoauriculofrontonasal syndrome", "Oculoauriculofrontonasal syndrome", "OCULOAURICULOFRONTONASAL DYSPLASIA", "oculoauriculofrontonasal dysplasia", "Oculoauriculofrontonasal dysplasia", "OAFNS - oculoauriculofrontonasal syndrome", "Oculoauriculofrontonasal syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculoauriculofrontonasal syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C0947964", "names": ["Genital Bleeding", "Reproductive System Hemorrhage", "Reproductive system hemorrhages", "Reproductive system haemorrhages"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reproductive System Hemorrhage", "shortest_name_length": 16}
{"curie": "UMLS:C4329380", "names": ["B-ALL with iAMP21", "B Acute Lymphoblastic Leukemia with iAMP21", "B Acute Lymphoblastic Leukemia with Intrachromosomal Amplification of Chromosome 21"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "B Acute Lymphoblastic Leukemia with Intrachromosomal Amplification of Chromosome 21", "shortest_name_length": 17}
{"curie": "UMLS:C0859871", "names": ["Nasal stinging", "Stinging of nose"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nasal stinging", "shortest_name_length": 14}
{"curie": "MONDO:0018662", "names": ["brachyolmia, Hobaek/Toledo type", "autosomal recessive brachyolmia", "brachyolmia, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive brachyolmia", "shortest_name_length": 31}
{"curie": "MONDO:0014999", "names": ["STHAG9", "GREM2 tooth agenesis", "tooth agenesis, selective, 9", "TOOTH AGENESIS, SELECTIVE, 9", "tooth agenesis, selective, type 9", "tooth agenesis, selective, 9; STHAG9", "tooth agenesis caused by mutation in GREM2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tooth agenesis, selective, 9", "shortest_name_length": 6}
{"curie": "UMLS:C5208200", "names": ["Steroid dependence", "Steroid dependence (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Steroid dependence", "shortest_name_length": 18}
{"curie": "UMLS:C5420748", "names": ["RADICULONEUROPATHY", "Radiculoneuropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Radiculoneuropathy", "shortest_name_length": 18}
{"curie": "MONDO:0021531", "names": ["lung fibroma", "Lung Fibroma", "Lung fibroma", "Fibroma of Lung", "Fibroma of lung", "fibroma of lung", "Pulmonary fibroma", "pulmonary fibroma", "Pulmonary Fibroma", "Fibroma of the Lung", "fibroma of the lung", "Fibroma of lung (disorder)", "fibroma of lung (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibroma of lung", "shortest_name_length": 12}
{"curie": "MONDO:0010266", "names": ["MRX58", "XLID58", "X-linked mental retardation 58", "Mental Retardation, X-Linked 58", "MENTAL RETARDATION, X-LINKED 58", "mental retardation, X-linked 58", "mental retardation, X-linked type 58", "intellectual disability, X-linked 58", "intellectual disability, X-linked type 58", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 58", "non-syndromic X-linked intellectual disability 58", "TSPAN7 non-syndromic X-linked intellectual disability", "intellectual developmental disorder, X-linked 58, X-linked recessive", "non-syndromic X-linked intellectual disability caused by mutation in TSPAN7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 58", "shortest_name_length": 5}
{"curie": "UMLS:C0279727", "names": ["pancreatic delta cell carcinoma", "Pancreatic Delta Cell Carcinoma", "carcinoma, pancreatic delta cell", "somatostatin secreting carcinoma", "somatostatin producing carcinoma", "pancreatic D islet cell carcinoma", "carcinoma, delta cell, pancreatic", "carcinoma, somatostatin producing", "Malignant Pancreatic Somatostatinoma", "Pancreatic Malignant Somatostatinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Pancreatic Somatostatinoma", "shortest_name_length": 31}
{"curie": "MONDO:0008030", "names": ["FMD", "FSHD", "FSHD1", "FSHD1A", "FSHMD1A", "Landouzy-Dejerine muscular dystrophy", "Landouzy-dejerine muscular dystrophy", "facioscapulohumeral muscular dystrophy", "muscular dystrophy, facioscapulohumeral", "FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1", "facioscapulohumeral muscular dystrophy 1", "Facioscapulohumeral Muscular Dystrophy 1", "facioscapulohumeral muscular dystrophy 1A", "Facioscapulohumeral muscular dystrophy 1a", "FRG1 facioscapulohumeral muscular dystrophy", "facioscapulohumeral muscular dystrophy type 1", "facioscapulohumeral muscular dystrophy type 1A", "MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1", "muscular dystrophy, facioscapulohumeral, type 1", "Muscular dystrophy, facioscapulohumeral, type 1a", "muscular dystrophy, facioscapulohumeral, type 1A", "MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1A", "Facioscapulohumeral muscular dystrophy, infantile", "FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY, INFANTILE", "facioscapulohumeral muscular dystrophy, infantile", "facioscapulohumeral muscular dystrophy type 1 (diagnosis)", "facioscapulohumeral muscular dystrophy caused by mutation in FRG1", "Landouzy-Dejerine muscular dystrophy facioscapulohumeral muscular dystrophy, infantile, included", "FACIOSCAPULOHUMERAL DYSTROPHY WITH SENSORINEURAL HEARING LOSS AND TORTUOSITY OF RETINAL ARTERIOLES", "Facioscapulohumeral dystrophy with sensorineural hearing loss and tortuosity of retinal arterioles", "facioscapulohumeral dystrophy with sensorineural hearing loss and tortuosity of retinal arterioles", "facioscapulohumeral dystrophy with sensorineural hearing loss and tortuosity of retinal arterioles, included"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "facioscapulohumeral muscular dystrophy 1", "shortest_name_length": 3}
{"curie": "MONDO:0032570", "names": ["JBTS35", "JOUBERT SYNDROME 35", "Joubert syndrome 35"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome 35", "shortest_name_length": 6}
{"curie": "UMLS:C1332178", "names": ["Acute Leukemia in Remission", "Adult Acute Leukemia in Remission"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Acute Leukemia in Remission", "shortest_name_length": 27}
{"curie": "MONDO:0032726", "names": ["COXPD39", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 39", "combined oxidative phosphorylation deficiency 39", "Combined oxidative phosphorylation defect type 39", "GFM2-related combined oxidative phosphorylation defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation deficiency 39", "shortest_name_length": 7}
{"curie": "MONDO:0017999", "names": ["FAHN", "Spastic Paraplegia 35", "Spastic paraplegia 35", "FATTY ACID HYDROXYLASE-ASSOCIATED NEURODEGENERATION", "fatty acid hydroxylase-associated neurodegeneration", "Fatty acid hydroxylase-associated neurodegeneration", "Fatty acid hydroxylase associated neurodegeneration", "Fatty Acid Hydroxylase-Associated Neurodegeneration", "Dysmyelinating leukodystrophy and spastic paraparesis", "Dysmyelinating Leukodystrophy and Spastic Paraparesis", "Fatty acid hydroxylase associated neurodegeneration (disorder)", "Spastic Paraplegia 35, Autosomal Recessive, with or without Neurodegeneration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fatty acid hydroxylase-associated neurodegeneration", "shortest_name_length": 4}
{"curie": "UMLS:C4525086", "names": ["Stage I Colorectal Cancer AJCC v8", "Stage I Colorectal Carcinoma AJCC v8", "Stage I Colorectal (Colon or Rectal) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Colorectal Cancer AJCC v8", "shortest_name_length": 33}
{"curie": "MONDO:0017389", "names": ["BH4-responsive HPA/PKU", "tetrahydrobiopterin-responsive HPA/PKU", "BH4-responsive hyperphenylalaninemia/phenylketonuria", "tetrahydrobiopterin-responsive hyperphenylalaninemia/phenylketonuria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tetrahydrobiopterin-responsive hyperphenylalaninemia/phenylketonuria", "shortest_name_length": 22}
{"curie": "MONDO:0019086", "names": ["ESCA", "esophageal cancer", "ESOPHAGEAL CANCER", "Esophageal Cancer", "esophagus carcinoma", "Cancer of Esophagus", "Esophagus Carcinoma", "carcinoma esophagus", "cancer of esophagus", "ESOPHAGUS, CARCINOMA", "Esophageal carcinoma", "carcinoma esophageal", "esophageal carcinoma", "carcinoma oesophagus", "Esophageal Carcinoma", "ESOPHAGEAL CARCINOMA", "cancer of oesophagus", "Carcinoma;oesophagus", "OESOPHAGEAL CARCINOMA", "oesophageal carcinoma", "Oesophageal carcinoma", "Carcinoma of esophagus", "carcinoma of esophagus", "CARCINOMA OF ESOPHAGUS", "Esophageal cancer, NOS", "Carcinoma of Esophagus", "esophageal cancer, NOS", "Carcinoma of oesophagus", "CARCINOMA OF OESOPHAGUS", "cancer of the esophagus", "Cancer of the Esophagus", "carcinoma of oesophagus", "Esophageal carcinoma NOS", "Oesophageal carcinoma NOS", "Carcinoma of esophagus NOS", "Carcinoma of the Esophagus", "carcinoma of the esophagus", "carcinoma esophageal cancer", "carcinoma of the oesophagus", "Carcinoma of oesophagus NOS", "ESOPHAGEAL CANCER, CARCINOMA", "Carcinoma of esophagus (disorder)", "carcinoma of esophagus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma of esophagus", "shortest_name_length": 4}
{"curie": "MONDO:0005867", "names": ["PPLO", "pplo", "Endemic pneumonia", "Mycoplasma pneumonia", "Mycoplasma Pneumonia", "mycoplasma pneumonia", "pneumonia mycoplasma", "MYCOPLASMA PNEUMONIA", "Pneumonia mycoplasmal", "mycoplasmas pneumonia", "Mycoplasma; pneumonia", "Mycoplasmal Pneumonia", "Eaton agent pneumonia", "Pneumonia, Mycoplasma", "mycoplasmal pneumonia", "Mycoplasmal pneumonia", "pneumonia; Mycoplasma", "Pneumonia due to PPLO", "Mycoplasma Pneumonias", "PNEUMONIA, EATON AGENT", "Pneumonias, Mycoplasma", "PNEUMONIA, MYCOPLASMAL", "Eatons agent pneumonia", "Eaton's agent pneumonia", "Eaton's agent; pneumonia", "pneumonia; Eaton's agent", "Primary Atypical Pneumonia", "primary atypical pneumonia", "Pneumonia primary atypical", "Primary atypical pneumonia", "Atypical Pneumonia, Primary", "Primary Atypical Pneumonias", "Pneumonia, Primary Atypical", "PNEUMONIA, PRIMARY ATYPICAL", "Atypical Pneumonias, Primary", "Pneumonias, Primary Atypical", "pneumonia due to Eaton's agent", "Pneumonia due to Eaton's agent", "Mycoplasma pneumoniae pneumonia", "Mycoplasma pneumonia (diagnosis)", "PAP due to Mycoplasma pneumoniae", "cold agglutinin positive pneumonia", "PNEUMONIA, COLD AGGLUTININ POSITIVE", "pneumonia due to Mycoplasma pneumoniae", "Pneumonia due to mycoplasma pneumoniae", "Pneumonia due to Mycoplasma pneumoniae", "primary atypical Mycoplasma pneumoniae", "Pneumonia caused by Mycoplasma pneumoniae", "Pneumonia caused by Genus Mycoplasma (disorder)", "Pneumonia due to Mycoplasma pneumoniae (disorder)", "pneumonia due to Mycoplasma pneumoniae (disorder)", "Primary atypical pneumonia (PAP) due to mycoplasma", "Pneumonia caused by Mycoplasma pneumoniae (disorder)", "Primary atypical pneumonia due to Mycoplasma pneumoniae", "Primary atypical pneumonia caused by Mycoplasma pneumoniae"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mycoplasma pneumoniae pneumonia", "shortest_name_length": 4}
{"curie": "MONDO:0009836", "names": ["pancreatitis, sclerosing cholangitis, and sicca complex", "PANCREATITIS, SCLEROSING CHOLANGITIS, AND SICCA COMPLEX", "Pancreatitis, Sclerosing Cholangitis, and Sicca Complex"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatitis, sclerosing cholangitis, and sicca complex", "shortest_name_length": 55}
{"curie": "MONDO:0004488", "names": ["Cervical Atypical Polypoid Adenomyoma", "cervical atypical polypoid adenomyoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical atypical polypoid adenomyoma", "shortest_name_length": 37}
{"curie": "UMLS:C0151661", "names": ["PERIPHERAL GANGRENE", "peripheral gangrene", "Peripheral gangrene", "GANGRENE PERIPHERAL", "Gangrene peripheral", "Peripheral gangrene (disorder)", "peripheral gangrene (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peripheral gangrene", "shortest_name_length": 19}
{"curie": "UMLS:C1333061", "names": ["Classic Type Trichoepithelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Classic Type Trichoepithelioma", "shortest_name_length": 30}
{"curie": "UMLS:C5419080", "names": ["Locally Advanced Fibrosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Fibrosarcoma", "shortest_name_length": 29}
{"curie": "MONDO:0005286", "names": ["palate tumor", "Palate Tumor", "tumor palate", "PALATE TUMOR", "palate tumors", "Palate--Tumors", "Palate neoplasm", "Palate Neoplasm", "tumor of palate", "palate neoplasm", "Tumor of Palate", "Tumor of palate", "palatal neoplasm", "Tumour of palate", "Palatal Neoplasm", "Palatal Neoplasms", "Neoplasm, Palatal", "Neoplasm of palate", "Neoplasms, Palatal", "Neoplasm of Palate", "neoplasm of palate", "Tumor of the Palate", "tumor of the palate", "Neoplasm of the Palate", "neoplasm of the palate", "secondary palate tumor", "tumor of secondary palate", "secondary palate neoplasm", "neoplasm of secondary palate", "Neoplasm of palate (disorder)", "neoplasm of palate (diagnosis)", "secondary palate neoplasm (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "palatal neoplasm", "shortest_name_length": 12}
{"curie": "MONDO:0013047", "names": ["GSD11", "GSD XI", "GSD 11", "GSD type 11", "glycogenosis type 11", "LDH-M subunit deficiency", "GLYCOGEN STORAGE DISEASE XI", "glycogen storage disease XI", "LDHA glycogen storage disease", "glycogen storage disease type 11", "LACTATE DEHYDROGENASE A DEFICIENCY", "Lactate dehydrogenase A deficiency", "Lactate Dehydrogenase A Deficiency", "lactate dehydrogenase A deficiency", "lactate dehydrogenase deficiency type A", "Lactate dehydrogenase deficiency type A", "glycogen storage disease caused by mutation in LDHA", "GSD due to lactate dehydrogenase M-subunit deficiency", "Glycogenosis due to lactate dehydrogenase M-subunit deficiency", "glycogenosis due to lactate dehydrogenase M-subunit deficiency", "glycogen storage disease due to lactate dehydrogenase M-subunit deficiency", "Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glycogen storage disease due to lactate dehydrogenase M-subunit deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0018914", "names": ["HTS", "hypotrichosis simplex", "Hypotrichosis simplex", "hereditary hypotrichosis simplex", "Hereditary hypotrichosis simplex", "Hereditary hypotrichosis simplex (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotrichosis simplex", "shortest_name_length": 3}
{"curie": "EFO:1000651", "names": ["recalcitrant atopic dermatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "recalcitrant atopic dermatitis", "shortest_name_length": 30}
{"curie": "UMLS:C4521872", "names": ["Stage I Pancreatic Cancer", "Stage I Pancreatic Cancer AJCC v8", "Stage I Exocrine Pancreatic Cancer AJCC v8", "Stage I Exocrine Pancreatic Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Pancreatic Cancer AJCC v8", "shortest_name_length": 25}
{"curie": "MONDO:0030962", "names": ["NPHS23", "nephrotic syndrome type 23", "NEPHROTIC SYNDROME, TYPE 23", "nephrotic syndrome, type 23"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrotic syndrome, type 23", "shortest_name_length": 6}
{"curie": "UMLS:C1518191", "names": ["Malignant Lymphoma by Cell Type (Working Formulation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Lymphoma by Cell Type (Working Formulation)", "shortest_name_length": 53}
{"curie": "MONDO:0043075", "names": ["Maccario Mena weir syndrome", "Maccario Mena Weir syndrome", "neuroaxonal dystrophy renal tubular acidosis", "Neuroaxonal dystrophy renal tubular acidosis", "CNS disorder characterized by severe behavioral retardation, hypotonia, inability to talk, marked tremors, gait disturbances and inability to concentr"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuroaxonal dystrophy renal tubular acidosis", "shortest_name_length": 27}
{"curie": "MONDO:0019306", "names": ["LI", "CIE", "Collodion baby", "alligator skin", "collodion baby", "Lamellar Ichthyose", "Ichthyose, Lamellar", "lamellar ichthyosis", "Lamellar ichthyosis", "Lamellar Ichthyoses", "Lamellar Ichthyosis", "ichthyosis lamellar", "Ichthyosis, Lamellar", "Ichthyosis, lamellar", "lamellar; ichthyosis", "ichthyosis; lamellar", "Ichthyoses, Lamellar", "congenital ichthyosis", "Ichthyosis, congenital", "Ichthyosis lammellaris", "Collodion baby syndrome", "erythrodermic ichthyosis", "Erythrodermic ichthyosis", "ichthyosiform erythroderma", "Classic lamellar ichthyosis", "Congenital lamellar ichthyosis", "Lamellar ichthyosis (disorder)", "Lamellar ichthyosis (diagnosis)", "Nonbullous congenital ichthyosis", "Congenital non-bullous ichthyosis", "Lamellar desquamation of the newborn", "lamellar desquamation of the newborn", "Ichthyosis, congenital, nonblistering", "congenital ichthyosiform erythroderma", "Nonbullous Erythroderma Ichthyosiforme", "Ichthyosiforme, Nonbullous Erythroderma", "Nonbullous Erythroderma Ichthyosiformes", "Erythroderma Ichthyosiforme, Nonbullous", "Ichthyosiformes, Nonbullous Erythroderma", "Erythroderma Ichthyosiformes, Nonbullous", "Nonbullous Congenital Lamellar Ichthyosis", "congenital ichthyosiform erythroderma (disease)", "Congenital nonbullous ichthyosiform erythroderma", "Congenital Nonbullous Ichthyosiform Erythroderma", "Nonbullous congenital ichthyosiform erythroderma", "Nonbullous Congenital Ichthyosiform Erythroderma", "nonbullous congenital ichthyosiform erythroderma", "congenital non-bullous ichthyosiform erythroderma", "congenital non bullous ichthyosiform erythroderma", "Ichthyosiform Erythroderma, Nonbullous Congenital", "non-bullous congenital ichthyosiform erythroderma", "Congenital non bullous ichthyosiform erythroderma", "Non-bullous congenital ichthyosiform erythroderma", "Congenital Ichthyosiform Erythroderma, Nonbullous", "Congenital non-bullous ichthyosiform erythroderma", "Congenital ichthyosiform erythroderma, non-bullous", "Congenital non bullous ichthyosiform erythroderma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital non-bullous ichthyosiform erythroderma", "shortest_name_length": 2}
{"curie": "MONDO:0004925", "names": ["DACRYOCYSTITIS CHRONIC", "chronic dacryocystitis", "Chronic dacryocystitis", "dacryocystitis; chronic", "dacryocystitis, chronic", "chronic; dacryocystitis", "DACRYOCYSTITIS, CHRONIC", "chronic; dacryopericystitis", "dacryopericystitis; chronic", "Chronic dacryocystitis (disorder)", "chronic dacryocystitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic dacryocystitis", "shortest_name_length": 22}
{"curie": "MONDO:0009748", "names": ["HSAN with spastic paraplegia", "hereditary sensory and autonomic neuropathy with spastic paraplegia", "Hereditary sensory and autonomic neuropathy with spastic paraplegia", "HSAN (hereditary sensory and autonomic neuropathy) with spastic paraplegia", "NEUROPATHY, HEREDITARY SENSORY, WITH SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE", "Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive", "neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive", "Hereditary sensory and autonomic neuropathy with spastic paraplegia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary sensory and autonomic neuropathy with spastic paraplegia", "shortest_name_length": 28}
{"curie": "UMLS:C4721656", "names": ["Stage IV Ovarian Dysgerminoma", "Stage IV Ovarian Dysgerminoma AJCC v7", "Stage IV Ovarian Dysgerminoma AJCC v6", "Stage IV Ovarian Dysgerminoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Ovarian Dysgerminoma AJCC v6 and v7", "shortest_name_length": 29}
{"curie": "UMLS:C2004458", "names": ["Melanocytoma", "melanocytoma", "Melanocytoma, NOS", "Magnocellular nevus", "Ocular melanocytoma", "ocular melanocytoma", "Magnocellular Nevus", "Magnocellular naevus", "Melanocytoma, eyeball", "melanocytoma; eyeball", "Optic Disc Melanocytoma", "Melanocytoma of Eyeball", "Melanocytoma of the eyeball", "Melanocytoma of the Eyeball", "ocular melanocytoma (diagnosis)", "magnocellular; nevus, unspecified site", "nevus; magnocellular, unspecified site", "Magnocellular nevus (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Magnocellular nevus", "shortest_name_length": 12}
{"curie": "MONDO:0017942", "names": ["Hendra virus infection", "Hendra henipavirus infectious disease", "Hendra henipavirus disease or disorder", "Hendra henipavirus caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hendra virus infection", "shortest_name_length": 22}
{"curie": "UMLS:C4054362", "names": ["Toxoplasmosis Associated Nephrotic Syndrome", "Nephrotic Syndrome - Toxoplasmosis Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - Toxoplasmosis Associated", "shortest_name_length": 43}
{"curie": "MONDO:0017460", "names": ["mitten hand", "Mitten hand", "syndactyly type 6", "Syndactyly type 6", "Syndactyly mitten type", "Syndactyly, mitten type", "syndactyly, mitten type", "Syndactyly type 6 (disorder)", "syndactyly type 6 (diagnosis)", "Unilateral syndactyly of digits 2-5", "unilateral syndactyly of digits 2-5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndactyly type 6", "shortest_name_length": 11}
{"curie": "MONDO:0005027", "names": ["sz", "Fit", "fit", "fits", "fit's", "fitted", "Fit(s)", "SEIZURE", "Fitting", "seizure", "Seizure", "Seizures", "Fits NOS", "Epilepsy", "epilepsy", "seizures", "Fit, NOS", "FITS NOS", "EPILEPSY", "epileptic", "epilepsis", "seizure d", "Epileptic", "epilepsia", "epilepsies", "CONVULSION", "Convulsion", "epileptics", "Epilepsies", "convulsion", "convulsions", "CONVULSIONS", "Seizure NOS", "Convulsions", "Seizure, NOS", "Epilepsy NOS", "EP - Epilepsy", "epileptic fit", "Epilepsy, NOS", "epilepsy; fit", "Epileptic fit", "fit; epileptic", "epileptic fits", "epilepsy types", "Convulsions NOS", "morbus; caducus", "convulsions nos", "Convulsion, NOS", "caducus; morbus", "Seizure syndrome", "Seizure Disorder", "epileptic attack", "seizure syndrome", "syndrome seizure", "Epileptic attack", "disorder seizure", "SEIZURE DISORDER", "CONVULSION (NOS)", "Seizure disorder", "Fit - convulsion", "seizure disorder", "attacks epileptic", "seizures syndrome", "disorder epilepsy", "Epileptic seizure", "epilepsy syndrome", "epileptic seizure", "Seizure Syndromes", "Seizure Disorders", "disorder seizures", "Seizure (finding)", "Seizure;epileptic", "seizure disorders", "seizure epileptic", "Epileptic Seizure", "Types of epilepsy", "disorders seizure", "epilepsy; seizure", "epileptic seizures", "Epileptic Seizures", "Epileptic fits NOS", "epilepsy; cortical", "seizure; epileptic", "Convulsion/Seizure", "EF - Epileptic fit", "disorders seizures", "Seizure, Epileptic", "Epilepsy all types", "Fits - convulsions", "epilepsy; cerebral", "Epileptic disorder", "epileptic syndrome", "seizures syndromes", "Epilepsy (disorder)", "Seizures, Epileptic", "epileptic; syndrome", "disorders epileptic", "cerebral; epileptic", "syndrome; epileptic", "Epileptic fits, NOS", "Epileptic convulsion", "epilepsy (diagnosis)", "Seizure disorder NOS", "convulsion epileptic", "Epilepsy, unspecified", "Epileptic attack, NOS", "convulsions (symptom)", "convulsions; epileptic", "epileptic; convulsions", "Epileptic seizures NOS", "Epileptic disorder, NOS", "Epileptic seizures, NOS", "Epileptic convulsions NOS", "seizure (physical finding)", "Epileptic convulsions, NOS", "Epileptic seizure (finding)", "Seizure disorder (disorder)", "CLINICAL EPILEPSY DIAGNOSES", "CLINICAL EPILEPTIC SYNDROMES AND SEIZURES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy", "shortest_name_length": 2}
{"curie": "UMLS:C1334207", "names": ["Intermediate Blood Vessel Tumor", "Intermediate Blood Vessel Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intermediate Blood Vessel Neoplasm", "shortest_name_length": 31}
{"curie": "MONDO:0013567", "names": ["ASD3", "Atrial Septal Defect 3", "ATRIAL SEPTAL DEFECT 3", "atrial septal defect 3", "atrial septal defect type 3", "atrial heart septal defect 3", "atrial septal defect3 - ASD3", "MYH6 atrial heart septal defect", "atrial heart septal defect type 3", "atrial septal defect3 - ASD3 (diagnosis)", "atrial heart septal defect caused by mutation in MYH6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atrial septal defect 3", "shortest_name_length": 4}
{"curie": "MONDO:0006977", "names": ["Spermatocele", "SPERMATOCELE", "spermatocele", "spermatocoele", "spermatoceles", "Spermatoceles", "Spermatic cyst", "cyst epididymal", "epididymis cyst", "Cyst;epididymal", "epididymal cyst", "Epididymal Cyst", "cyst epididymis", "EPIDIDYMAL CYST", "Epididymal cyst", "Cyst, Epididymal", "cysts epididymis", "cysts epididymal", "epididymis; cyst", "cyst; epididymis", "Epididymal cysts", "EPIDIDYMIS, CYST", "Epididymal Cysts", "Cysts, Epididymal", "Cyst of epididymis", "cyst of epididymis", "Cyst of Epididymis", "Cyst of the Epididymis", "epididymis spermatocele", "Spermatocele (disorder)", "Spermatocele, epididymis", "spermatocele (diagnosis)", "Spermatocele of epididymis", "Cyst of epididymis (disorder)", "cyst of epididymis (diagnosis)", "spermatocele (physical finding)", "epididymis spermatocele (___ cm)", "Spermatocele of epididymis, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatocele", "shortest_name_length": 12}
{"curie": "UMLS:C5419543", "names": ["Metastatic Intrahepatic Cholangiocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Intrahepatic Cholangiocarcinoma", "shortest_name_length": 42}
{"curie": "MONDO:0019115", "names": ["BMIQ20", "OBESITY", "MC4R DEFICIENCY", "MC4R Deficiency", "MC4R deficiency", "OBESITY, RESISTANCE TO", "Melanocortin 4 Receptor Deficiency", "Melanocortin 4 receptor deficiency", "MELANOCORTIN 4 RECEPTOR DEFICIENCY", "BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 20", "obesity due to melanocortin 4 receptor deficiency", "Obesity due to melanocortin 4 receptor deficiency", "Obesity due to melanocortin 4 receptor deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "obesity due to melanocortin 4 receptor deficiency", "shortest_name_length": 6}
{"curie": "UMLS:C5554550", "names": ["Uterine Ligament Papillary Cystadenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Ligament Papillary Cystadenoma", "shortest_name_length": 38}
{"curie": "UMLS:C0160680", "names": ["a.carotis; injury", "trauma carotid artery", "injury carotid artery", "carotid artery injury", "Carotid Artery Trauma", "Carotid Artery Injury", "Carotid artery injury", "Trauma, Carotid Artery", "Injury, Carotid Artery", "Artery Injury, Carotid", "Artery Trauma, Carotid", "injury; carotid artery", "Carotid Artery Injuries", "Injury to carotid artery", "Artery Injuries, Carotid", "Injury to Carotid Artery", "Injuries, Carotid Artery", "Injury of carotid artery", "injury of carotid artery", "Injury of carotid artery NOS", "Injury of carotid artery, NOS", "Traumatic Carotid Arteriopathy", "Carotid Arteriopathy, Traumatic", "Carotid Arteriopathies, Traumatic", "Injury of carotid artery (disorder)", "injury of carotid artery (diagnosis)", "Unspecified injury of carotid artery", "Injury of carotid artery, unspecified", "Injury to carotid artery, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carotid Artery Injuries", "shortest_name_length": 17}
{"curie": "MONDO:0007619", "names": ["ADG", "ADERM", "Adermatoglyphia", "adermatoglyphia", "ADERMATOGLYPHIA", "Absence of fingerprints", "absence of fingerprints", "Fingerprints, Absence of", "fingerprints, absence of", "FINGERPRINTS, ABSENCE OF", "immigration delay disease", "Immigration delay disease", "congenital absence of fingerprints", "Congenital absence of fingerprints", "isolated congenital adermatoglyphia", "Isolated congenital adermatoglyphia", "Isolated congenital adermatoglyphia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated congenital adermatoglyphia", "shortest_name_length": 3}
{"curie": "MONDO:0018081", "names": ["Hantavirosis", "Hantavirus fever", "Hemorrhagic fever-renal syndrome", "hemorrhagic fever-renal syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemorrhagic fever-renal syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0016518", "names": ["isolated punctate PPK", "isolated punctate palmoplantar keratoderma", "isolated punctate palmoplantar hyperkeratosis", "nonsyndromic punctate palmoplantar keratoderma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated punctate palmoplantar keratoderma", "shortest_name_length": 21}
{"curie": "UMLS:C0522757", "names": ["toxic; agent, exposure", "Exposure to toxic agent", "Exposure to toxic agents, NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Exposure to toxic agent", "shortest_name_length": 22}
{"curie": "MONDO:0014606", "names": ["WHSUS", "MRD37", "WHITE-Sutton syndrome", "WHITE-SUTTON SYNDROME", "White-Sutton syndrome", "White Sutton syndrome", "White Sutton syndrome (disorder)", "White Sutton syndrome (diagnosis)", "autosomal dominant mental retardation 37", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 37", "mental retardation, autosomal dominant 37", "autosomal dominant intellectual disability 37", "intellectual disability, autosomal dominant 37", "mental retardation, autosomal dominant type 37", "intellectual disability, autosomal dominant type 37", "intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome", "Intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0009229", "names": ["HFS", "Murray Syndrome", "Syndrome, Murray", "Puretic Syndrome", "Puretic syndrome", "puretic syndrome", "Syndrome, Puretic", "Puretic Syndromes", "Syndromes, Puretic", "Systemic Hyalinoses", "Systemic hyalinosis", "Juvenile Hyalinoses", "systemic hyalinosis", "Juvenile Hyalinosis", "Systemic Hyalinosis", "Hyalinosis, Juvenile", "Hyalinoses, Juvenile", "Hyalinoses, Systemic", "Hyalinosis, Systemic", "HYALINOSIS, SYSTEMIC", "hyalinosis, systemic", "Systemic Juvenile Hyalinosis", "Systemic Juvenile Hyalinoses", "Hyalinosis, Systemic Juvenile", "Hyalinoses, Systemic Juvenile", "Hyaline Fibromatosis Juvenile", "hyaline fibromatosis syndrome", "Juvenile Hyalinosis, Systemic", "Juvenile Hyaline Fibromatosis", "Hyaline Fibromatosis Syndrome", "Juvenile Hyaline Fibromatoses", "Fibromatosis Juvenile Hyaline", "Hyaline fibromatosis syndrome", "Juvenile Hyalinoses, Systemic", "HYALINE FIBROMATOSIS SYNDROME", "Juvenile hyaline fibromatosis", "Infantile systemic hyalinosis", "inherited systemic hyalinosis", "Infantile Systemic Hyalinosis", "Infantile Systemic Hyalinoses", "Systemic Hyalinoses, Infantile", "Hyalinoses, Infantile Systemic", "Fibromatosis, Juvenile Hyaline", "Hyalinosis, Infantile Systemic", "Hyaline Fibromatosis Syndromes", "Systemic Hyalinosis, Infantile", "Fibromatosis Syndrome, Hyaline", "Syndrome, Hyaline Fibromatosis", "Hyaline Fibromatosis, Juvenile", "Syndromes, Hyaline Fibromatosis", "Fibromatosis Syndromes, Hyaline", "Murray Puretic Drescher syndrome", "Murray-Puretic-Drescher syndrome", "Juvenile hyaline fibromatosis (disorder)", "Hyaline fibromatosis syndrome (disorder)", "Fibromatosis Hyalinica Multiplex Juvenilis", "juvenile hyaline fibromatosis (former subtype)", "infantile systemic hyalinosis (former subtype)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyaline fibromatosis syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C0577708", "names": ["urinary tract infection e coli", "URINARY TRACT INFECTION E COLI", "e coli urinary tract infection", "coli e infections tract urinary", "Escherichia coli urinary tract infection", "urinary tract infection Escherichia coli", "Urinary tract infection caused by Escherichia coli", "Escherichia coli urinary tract infection (diagnosis)", "Urinary tract infection caused by Escherichia coli (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urinary tract infection caused by Escherichia coli", "shortest_name_length": 30}
{"curie": "UMLS:C5237413", "names": ["Refractory Skin Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Skin Squamous Cell Carcinoma", "shortest_name_length": 39}
{"curie": "EFO:0004269", "names": ["cardiac arrhythmia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cardiac arrhythmia", "shortest_name_length": 18}
{"curie": "UMLS:C3274280", "names": ["TAPVR Type III", "Type III Total Anomalous Pulmonary Venous Return", "Type III (Infradiaphragmatic/Infracardiac) Total Anomalous Pulmonary Venous Return", "Total Anomalous Pulmonary Venous Return, Type III (Infradiaphragmatic/Infracardiac)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Type III Total Anomalous Pulmonary Venous Return", "shortest_name_length": 14}
{"curie": "MONDO:0020338", "names": ["acquired PRCA", "Primary acquired PRCA", "Acquired red cell aplasia", "adult pure red cell aplasia", "adult pure red-cell aplasia", "Adult pure red cell aplasia", "acquired pure red cell aplasia", "Acquired Pure Red Cell Aplasia", "Acquired pure red cell aplasia", "pure red-cell aplasia of adults", "Pure red cell aplasia, acquired", "acquired red blood cell aplasia", "idiopathic pure red cell aplasia", "Acquired red cell aplasia (disorder)", "red blood cell aplasia acquired pure", "Primary acquired pure red cell aplasia", "Adult pure red cell aplasia (disorder)", "Adult pure red cell aplasia (diagnosis)", "red blood cell aplasia acquired pure adult", "Pure red cell aplasia, acquired (diagnosis)", "acquired red blood cell aplasia (diagnosis)", "Acquired pure red cell aplasia, unspecified", "Acquired pure red cell aplasia [erythroblastopenia]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult pure red cell aplasia", "shortest_name_length": 13}
{"curie": "UMLS:C5446568", "names": ["Advanced Nasopharyngeal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Nasopharyngeal Carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0008375", "names": ["Amotio retinae", "Detached retina", "retina detached", "detached retina", "retina, detached", "retina detachment", "Retina Detachment", "RETINA DETACHMENT", "retina; detachment", "Detachment;retinal", "RETINA, SEPARATION", "RETINA, DETACHMENT", "DETACHMENT RETINAL", "Retinal detachment", "RETINAL DETACHMENT", "Retinal Detachment", "retinal detachment", "DETACHMENT, RETINA", "detachment; retina", "Detachment retinal", "Detachment, Retinal", "Retinal detachments", "Retinal Detachments", "retinal detachments", "Detachments, Retinal", "Retinal detachment NOS", "Retinal detachment, NOS", "RD - Retinal detachment", "Retinal layer separation", "retinal layer separation", "Sensory retinal detachment", "separation; retinal layers", "retinal layers; separation", "Separation of retinal layers", "retina; separation of layers", "Retinal layer separation, NOS", "Retinal detachment (disorder)", "retinal detachment (diagnosis)", "Unspecified retinal detachment", "retinal layer separation (diagnosis)", "Retinal layer separation, unspecified", "retinal detachment (physical finding)", "Unspecified separation of retinal layers"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal detachment", "shortest_name_length": 14}
{"curie": "UMLS:C4745015", "names": ["Recurrent Acute Myeloid Leukemia with Recurrent Genetic Abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Acute Myeloid Leukemia with Recurrent Genetic Abnormalities", "shortest_name_length": 69}
{"curie": "UMLS:C4683018", "names": ["Stage IIIA Eyelid Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Eyelid Carcinoma AJCC v8", "shortest_name_length": 35}
{"curie": "EFO:0010177", "names": ["lobar intracerebral hemorrhage\"@e"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lobar intracerebral hemorrhage\"@e", "shortest_name_length": 33}
{"curie": "UMLS:C4526963", "names": ["Gastric and Omental GIST by AJCC v8 Stage", "Gastric and Omental Gastrointestinal Stromal Tumor by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric and Omental Gastrointestinal Stromal Tumor by AJCC v8 Stage", "shortest_name_length": 41}
{"curie": "MONDO:0020211", "names": ["syndromic keratoconus", "syndromic keratoconus (disease)", "syndrome associated with keratoconus (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic keratoconus", "shortest_name_length": 21}
{"curie": "UMLS:C0265656", "names": ["Hallux valgus", "hallux valgus", "HV - Hallux valgus", "hallux abductovalgus", "Hallux abductovalgus", "congenital hallux valgus", "Congenital hallux valgus", "Congenital Hallux Valgus", "valgus; hallux, congenital", "hallux; valgus, congenital", "HAV - Hallux abductovalgus", "Congenital hallux valgus (disorder)", "congenital hallux valgus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital hallux valgus", "shortest_name_length": 13}
{"curie": "UMLS:C0857117", "names": ["hand rash", "rash hand", "Hand rash", "hands rash"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hand rash", "shortest_name_length": 9}
{"curie": "UMLS:C4744689", "names": ["Recurrent Cytomegalovirus Infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Cytomegalovirus Infection", "shortest_name_length": 35}
{"curie": "MONDO:0015915", "names": ["cerebellar malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellar malformation", "shortest_name_length": 23}
{"curie": "UMLS:C0854286", "names": ["eyelid disorder function", "Eyelid Function Disorder", "Eyelid function disorder", "eyelid function disorder", "Eyelid function disorder NOS", "eyelid function disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eyelid Function Disorder", "shortest_name_length": 24}
{"curie": "MONDO:0007449", "names": ["Dermoodontodysplasia", "DERMOODONTODYSPLASIA", "Dermoodonto dysplasia", "dermoodonto dysplasia", "Dermo odontodysplasia", "dermo odontodysplasia", "dermo-odonto dysplasia", "dermo-odonto-dysplasia", "Dermo-odonto dysplasia", "Dermo-odonto dysplasia (disorder)", "ectodermal dysplasia, hair-nail-Tooth type", "ECTODERMAL DYSPLASIA, HAIR-NAIL-TOOTH TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dermo-odonto dysplasia", "shortest_name_length": 20}
{"curie": "UMLS:C5192106", "names": ["Solid tumor with NTRK gene fusion", "Solid tumour with NTRK gene fusion", "Solid tumor with neurotrophic receptor tyrosine kinase", "Solid tumour with neurotrophic receptor tyrosine kinase", "Solid neoplasm with neurotrophic receptor tyrosine kinase gene fusion", "Solid neoplasm with neurotrophic receptor tyrosine kinase gene fusion (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Solid neoplasm with neurotrophic receptor tyrosine kinase gene fusion", "shortest_name_length": 33}
{"curie": "MONDO:0014800", "names": ["SHPM", "myopathy, scapulohumeroperoneal", "MYOPATHY, SCAPULOHUMEROPERONEAL", "Progressive scapulohumeroperoneal distal myopathy", "progressive scapulohumeroperoneal distal myopathy", "Progressive scapulohumeroperoneal distal myopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive scapulohumeroperoneal distal myopathy", "shortest_name_length": 4}
{"curie": "MONDO:0012525", "names": ["LCA12", "Leber Congenital Amaurosis 12", "LEBER CONGENITAL AMAUROSIS 12", "Leber congenital amaurosis 12", "RD3 Leber congenital amaurosis", "Leber congenital amaurosis type 12", "amaurosis congenita of Leber, type 12", "LEBER CONGENITAL AMAUROSIS 12 (disorder)", "Leber congenital amaurosis caused by mutation in RD3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leber congenital amaurosis 12", "shortest_name_length": 5}
{"curie": "MONDO:0015419", "names": ["midline cervical cleft", "Midline cervical cleft", "Midline brainstem cleft", "Midline cervical webbing", "Pterygium colli medianum", "Midline brain stem cleft", "Median fissure of the neck", "Midline cleft in the brainstem", "Midline cervical cleft (disorder)", "Congenital midline cervical cleft"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "midline cervical cleft", "shortest_name_length": 22}
{"curie": "MONDO:0024382", "names": ["shift work disorder", "circadian rhythm sleep disorder, shift work type", "circadian rhythm sleep disorder of shift work type", "Circadian rhythm sleep disorder of shift work type", "Circadian rhythm sleep disorder of shift work type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "circadian rhythm sleep disorder, shift work type", "shortest_name_length": 19}
{"curie": "MONDO:0010504", "names": ["CDG2S", "IMD47", "CDGIIs", "CDG IIs", "IMMUNODEFICIENCY 47", "immunodeficiency 47", "immunodeficiency type 47", "immunodeficiency 47; IMD47", "immunodeficiency 47, X-linked recessive", "ATP6AP1 primary immunodeficiency disease", "congenital disorder of glycosylation type IIs", "CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIs", "primary immunodeficiency disease caused by mutation in ATP6AP1", "IMMUNODEFICIENCY AND HEPATOPATHY WITH OR WITHOUT NEUROLOGIC FEATURES", "immunodeficiency and hepatopathy with or without neurologic features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 47", "shortest_name_length": 5}
{"curie": "UMLS:C4727678", "names": ["Recurrent Chronic Myelomonocytic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Chronic Myelomonocytic Leukemia", "shortest_name_length": 41}
{"curie": "MONDO:0005126", "names": ["TT leprosy", "TT; leprosy", "leprosy; TT", "type T leprosy", "Type T leprosy", "smooth leprosy", "Smooth leprosy", "Nodular Leprosy", "Nodular leprosy", "Type TT leprosy", "LEPROSY, NODULAR", "nodular; leprosy", "leprosy; nodular", "Leprosy, Nodular", "Nodular Leprosies", "Cutaneous Leprosy", "Leprosies, Nodular", "Leprosy, Cutaneous", "leprosy tuberculoid", "Tuberculoid Leprosy", "Cutaneous Leprosies", "Tuberculoid leprosy", "tuberculoid leprosy", "TUBERCULOID LEPROSY", "Leprosies, Cutaneous", "tuberculoid; leprosy", "leprosy; tuberculoid", "Leprosy, Tuberculoid", "Tuberculoid Leprosies", "Leprosies, Tuberculoid", "Full tuberculoid leprosy", "Tuberculoid leprosy [type T]", "Tuberculoid leprosy (type t)", "tuberculoid leprosy [type T]", "TT - Full tuberculoid leprosy", "Tuberculoid leprosy (disorder)", "tuberculoid leprosy (diagnosis)", "Tuberculoid Hansen's disease (leprosy)", "Mycobacterium leprae infection (tuberculoid)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tuberculoid leprosy", "shortest_name_length": 10}
{"curie": "MONDO:0013136", "names": ["HYPTSV", "Hypotrichosis and recurrent skin vesicles", "HYPOTRICHOSIS AND RECURRENT SKIN VESICLES", "Hypotrichosis And Recurrent Skin Vesicles", "hypotrichosis and recurrent skin vesicles", "Hereditary hypotrichosis with recurrent skin vesicles", "hereditary hypotrichosis with recurrent skin vesicles", "Hereditary hypotrichosis with recurrent skin vesicles syndrome", "Hereditary hypotrichosis with recurrent skin vesicles syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary hypotrichosis with recurrent skin vesicles", "shortest_name_length": 6}
{"curie": "UMLS:C0543663", "names": ["Acquired Autoimmune Hemolytic Anemia", "Secondary autoimmune hemolytic anemia", "secondary autoimmune hemolytic anemia", "Idiopathic Autoimmune Hemolytic Anemia", "Autoimmune hemolytic anemia, secondary", "ANEMIA, HEMOLYTIC, ACQUIRED AUTOIMMUNE", "Secondary autoimmune haemolytic anaemia", "hemolytic; anemia, acquired, autoimmune", "anemia; hemolytic, acquired, autoimmune", "anemia; hemolytic, secondary, autoimmune", "hemolytic; anemia, secondary, autoimmune", "Secondary autoimmune hemolytic anemia (disorder)", "secondary autoimmune hemolytic anemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Idiopathic Autoimmune Hemolytic Anemia", "shortest_name_length": 36}
{"curie": "MONDO:0032632", "names": ["MC1DN28", "nuclear type mitochondrial complex I deficiency 28", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 28", "mitochondrial complex 1 deficiency, nuclear type 28"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 28", "shortest_name_length": 7}
{"curie": "MONDO:0018091", "names": ["Viljoen Kallis Voges syndrome", "Viljoen-Kallis-Voges syndrome", "microcephaly brachydactyly kyphoscoliosis", "microcephaly-brachydactyly-kyphoscoliosis syndrome", "Microcephaly-brachydactyly-kyphoscoliosis syndrome", "Microcephaly with brachydactyly and kyphoscoliosis syndrome", "Microcephalus with brachydactyly and kyphoscoliosis syndrome", "microcephalus with brachydactyly and kyphoscoliosis syndrome", "Microcephalus with brachydactyly and kyphoscoliosis syndrome (disorder)", "microcephalus with brachydactyly and kyphoscoliosis syndrome (diagnosis)", "microcephaly, short stature, brachydactyly type D, flattened occiput, low-set large ears, prominent nose, kyphoscoliosis and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly-brachydactyly-kyphoscoliosis syndrome", "shortest_name_length": 29}
{"curie": "MONDO:0018761", "names": ["SMARCA4-DTS", "SMARCA4-deficient thoracic sarcoma", "SMARCA4-deficient sarcoma of thorax", "Smarca4-deficient sarcoma of thorax"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SMARCA4-deficient sarcoma of thorax", "shortest_name_length": 11}
{"curie": "UMLS:C3888496", "names": ["Intestinal sepsis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal sepsis", "shortest_name_length": 17}
{"curie": "MONDO:0012377", "names": ["ASPG4", "Asperger syndrome susceptibility 4", "ASPERGER syndrome, susceptibility to, 4", "ASPERGER SYNDROME, SUSCEPTIBILITY TO, 4", "asperger syndrome, susceptibility to, 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "asperger syndrome, susceptibility to, 4", "shortest_name_length": 5}
{"curie": "UMLS:C4288371", "names": ["Primary Peritoneal Low-Grade Serous Adenocarcinoma", "Primary Peritoneal Low Grade Serous Adenocarcinoma", "Invasive Micropapillary Serous Carcinoma of the Peritoneum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Peritoneal Low Grade Serous Adenocarcinoma", "shortest_name_length": 50}
{"curie": "UMLS:C4329258", "names": ["Acquired Factor XII Deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acquired Factor XII Deficiency", "shortest_name_length": 30}
{"curie": "MONDO:0007796", "names": ["FIH", "FIH1", "hypoparathyroidism familial isolated", "hypoparathyroidism, familial isolated", "hypoparathyroidism, autosomal dominant", "hypoparathyroidism, familial isolated 1", "hypoparathyroidism, autosomal recessive", "HYPOPARATHYROIDISM, FAMILIAL ISOLATED, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypoparathyroidism, familial isolated 1", "shortest_name_length": 3}
{"curie": "UMLS:C1963732", "names": ["Hypercreatinemia", "Hypercreatinaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypercreatinaemia", "shortest_name_length": 16}
{"curie": "MONDO:0006364", "names": ["peritoneal WDPM", "Peritoneal WDPM", "Peritoneal WDPMT", "Peritoneal Well Differentiated Papillary Mesothelioma", "Peritoneal Well-Differentiated Papillary Mesothelioma", "peritoneal well differentiated papillary mesothelioma", "Peritoneal Well Differentiated Papillary Mesothelial Tumor", "Peritoneal Well-Differentiated Papillary Mesothelial Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peritoneal well differentiated papillary mesothelioma", "shortest_name_length": 15}
{"curie": "UMLS:C1328491", "names": ["Bile Duct Hemorrhage", "Hemorrhage of bile duct", "Hemorrhage in bile duct", "Haemorrhage of bile duct", "Haemorrhage in bile duct", "Hemorrhage of bile duct (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemorrhage in bile duct", "shortest_name_length": 20}
{"curie": "MONDO:0009509", "names": ["LKS", "CSWS", "FESD", "CSWSS", "ADRESD", "RESDAD", "CSWS syndrome", "CSWSS syndrome", "Landau-Kleffner Syndrome", "LANDAU-KLEFFNER SYNDROME", "landau kleffner syndrome", "Landau-Kleffner syndrome", "landau-Kleffner syndrome", "Landau Kleffner Syndrome", "landau-kleffner syndrome", "Syndrome, Landau-Kleffner", "Acquired epileptic aphasia", "Acquired Epileptic Aphasia", "acquired epileptic aphasia", "Aphasia, Acquired Epileptic", "Acquired Epileptic Aphasias", "Epileptic Aphasia, Acquired", "Aphasia, Epileptic, Acquired", "Epileptic Aphasias, Acquired", "Acquired Epileptiform Aphasia", "acquired epileptiform aphasia", "Epileptiform Aphasia, Acquired", "Acquired aphasia with epilepsy", "Acquired Epileptiform Aphasias", "Epileptiform Aphasias, Acquired", "aphasia, acquired, with epilepsy", "APHASIA, ACQUIRED, WITH EPILEPSY", "Aphasia, Acquired, with Epilepsy", "Aphasia co-occurrent with epilepsy", "Acquired epileptic aphasia (disorder)", "Acquired epileptic aphasia (diagnosis)", "FESD with or without Mental Retardation", "Continuous spikes and waves during sleep", "acquired aphasia with convulsive disorder", "Acquired Aphasia with Convulsive Disorder", "Aphasia, Acquired, With Convulsive Disorder", "Landau-Kleffner Acquired Epileptiform Aphasia", "Landau Kleffner Acquired Epileptiform Aphasia", "Acquired aphasia with epilepsy [Landau-Kleffner]", "Continuous spikes and waves during slow-wave sleep", "Acquired Childhoood Aphasia with Convulsive Disorder", "benign epilepsy of childhood with centrotemporal spikes", "Continuous spike and wave during slow wave sleep syndrome", "continuous Spike and waves during slow-Wave sleep syndrome", "CONTINUOUS SPIKE AND WAVES DURING SLOW-WAVE SLEEP SYNDROME", "developmental disorder - speech acquired epileptic aphasia", "Epileptic encephalopathy with continuous spike-and-wave during slow sleep", "epilepsy, focal, with speech disorder and with or without mental retardation", "Epilepsy, Focal, with Speech Disorder and with or without Mental Retardation", "EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION", "Rolandic Epilepsy, Mental Retardation, And Speech Dyspraxia, Autosomal Dominant", "ROLANDIC EPILEPSY, MENTAL RETARDATION, AND SPEECH DYSPRAXIA, AUTOSOMAL DOMINANT", "Rolandic epilepsy, mental retardation, and speech dyspraxia, autosomal dominant", "epilepsy, focal, with speech disorder and with or without intellectual disability", "Rolandic epilepsy, intellectual disability, and speech dyspraxia, autosomal dominant", "epilepsy, focal, with speech disorder and with or without impaired intellectual development", "EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT", "Rolandic Epilepsy, Intellectual Development Disorder, And Speech Dyspraxia, Autosomal Dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Landau-Kleffner syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C0751887", "names": ["Medullary Tumor", "medullary tumor", "Medullary Tumors", "Tumor, Medullary", "medullary tumors", "Tumors, Medullary", "Medullary Neoplasm", "Medullary Neoplasms", "Neoplasm, Medullary", "Neoplasms, Medullary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Medullary Neoplasms", "shortest_name_length": 15}
{"curie": "UMLS:C1336866", "names": ["Anaplastic Ureter Carcinoma", "Anaplastic Ureteral Carcinoma", "Anaplastic Carcinoma of Ureter", "anaplastic carcinoma of ureter", "Ureter Undifferentiated Carcinoma", "Undifferentiated Ureter Carcinoma", "Anaplastic Carcinoma of the Ureter", "Undifferentiated Ureteral Carcinoma", "undifferentiated carcinoma of ureter", "Undifferentiated Carcinoma of Ureter", "Undifferentiated Carcinoma of the Ureter", "anaplastic carcinoma of ureter (diagnosis)", "undifferentiated carcinoma of ureter (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anaplastic carcinoma of ureter", "shortest_name_length": 27}
{"curie": "MONDO:0021746", "names": ["Pyelocystitis", "Cystopyelitis", "cystopyelitis", "pyelocystitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyelocystitis", "shortest_name_length": 13}
{"curie": "MONDO:0000592", "names": ["specific delays in development", "specific developmental disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "specific developmental disorder", "shortest_name_length": 30}
{"curie": "MONDO:0012327", "names": ["DFNB46", "autosomal recessive deafness 46", "DEAFNESS, AUTOSOMAL RECESSIVE 46", "Deafness, Autosomal Recessive 46", "deafness, autosomal recessive 46", "autosomal recessive nonsyndromic deafness 46", "autosomal recessive nonsyndromic hearing loss 46", "autosomal recessive nonsyndromic deafness type 46"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 46", "shortest_name_length": 6}
{"curie": "MONDO:0004248", "names": ["infratentorial ependymoma", "Infratentorial Ependymoma", "Pediatric Infratentorial Ependymoma", "Childhood Infratentorial Ependymoma", "pediatric infratentorial ependymoma", "childhood infratentorial ependymoma", "infratentorial ependymoma, childhood", "ependymoma, infratentorial, childhood", "childhood infratentorial ependyoblastoma", "ependyoblastoma, childhood infratentorial", "infratentorial ependyoblastoma, childhood", "CNS tumor, childhood infratentorial ependymoma", "pediatric CNS tumor, infratentorial ependymoma", "childhood CNS tumor, infratentorial ependymoma", "CNS tumor, pediatric infratentorial ependymoma", "childhood brain tumor, infratentorial ependymoma", "brain tumor, childhood infratentorial ependymoma", "pediatric brain tumor, infratentorial ependymoma", "brain tumor, pediatric infratentorial ependymoma", "brain tumor, infratentorial ependymoma, childhood", "central nervous system tumor, infratentorial ependymoma, childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pediatric infratentorial ependymoma", "shortest_name_length": 25}
{"curie": "UMLS:C1112516", "names": ["Salivary duct inflammation", "Salivary Duct Inflammation", "salivary duct; inflammation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Salivary Duct Inflammation", "shortest_name_length": 26}
{"curie": "MONDO:0011162", "names": ["CAE3", "Cae3", "CZP3", "CTRCT14", "cataract 14 multiple types", "cataract 14, multiple types", "CATARACT 14, MULTIPLE TYPES", "zonular pulverulent cataract 3", "CATARACT, ZONULAR PULVERULENT 3", "Cataract, Zonular Pulverulent 3", "cataract, zonular pulverulent 3", "GJA3 early-onset non-syndromic cataract", "early-onset non-syndromic cataract caused by mutation in GJA3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 14 multiple types", "shortest_name_length": 4}
{"curie": "MONDO:0700092", "names": ["Child Mental Disorder", "Child Mental Disorders", "Mental Disorder, Child", "Disorder, Child Mental", "Mental Disorders, Child", "Neurodevelopmental disorder", "Neurodevelopmental Disorder", "neurodevelopmental disorder", "Disorder, Neurodevelopmental", "Neurodevelopmental disorders", "Neurodevelopmental Disorders", "Neurodevelopmental disorder\"@e", "Neurodevelopmental disorder NOS", "Social-emotional developmental delay", "Neurodevelopmental disorder (disorder)", "Mental Disorders Diagnosed in Childhood", "Neurodevelopmental disorder (diagnosis)", "Mental Disorders Usually Diagnosed in Infancy, Childhood or Adolescence", "Neurodevelopmental Disorders Usually Diagnosed in Infancy, Childhood or Adolescence"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurodevelopmental disorder", "shortest_name_length": 21}
{"curie": "UMLS:C5670474", "names": ["Supratentorial Ependymoma, NEC", "Supratentorial Ependymoma, Not Elsewhere Classified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Supratentorial Ependymoma, Not Elsewhere Classified", "shortest_name_length": 30}
{"curie": "UMLS:C0334482", "names": ["Fetal rhabdomyoma", "Fetal Rhabdomyoma", "rhabdomyoma; fetal", "fetal; rhabdomyoma", "Foetal rhabdomyoma", "Fetal rhabdomyoma (disorder)", "Fetal rhabdomyoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fetal rhabdomyoma", "shortest_name_length": 17}
{"curie": "UMLS:C0279631", "names": ["Acute Basophilic Leukemia", "adult acute basophilic leukemia", "Adult Acute Basophilic Leukemia", "acute basophilic leukemia, adult", "leukemia, adult acute basophilic", "basophilic leukemia, adult acute"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Acute Basophilic Leukemia", "shortest_name_length": 25}
{"curie": "UMLS:C0393554", "names": ["Amyotrophic lateral sclerosis with dementia", "Amyotrophic Lateral Sclerosis With Dementia", "amyotrophic lateral sclerosis with dementia", "Dementia With Amyotrophic Lateral Sclerosis", "Amyotrophic lateral sclerosis with dementia (disorder)", "amyotrophic lateral sclerosis with dementia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Amyotrophic Lateral Sclerosis With Dementia", "shortest_name_length": 43}
{"curie": "MONDO:0042370", "names": ["intestinal; yersiniosis", "yersiniosis; intestinal", "Yersinia enterocolitica infection", "YERSINIA ENTEROCOLITICA INFECTION", "Yersinia enterocolitica Infection", "Yersinia enterocolitica Infections", "Infection by Yersinia enterocolitica", "infection by Yersinia enterocolitica", "Yersinia enterocolitica infectious disease", "infection caused by Yersinia enterocolitica", "Infection caused by Yersinia enterocolitica", "infection; Yersinia enterocolica (intestine)", "Yersinia enterocolica; infection (intestine)", "Intestinal infection due to yersinia enterocolitica", "Infection caused by Yersinia enterocolitica (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Yersinia enterocolitica infectious disease", "shortest_name_length": 23}
{"curie": "UMLS:C4728187", "names": ["Steroid diabetes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Steroid diabetes", "shortest_name_length": 16}
{"curie": "MONDO:0017872", "names": ["Lujo virus infection", "Lujo hemorrhagic fever", "lujo hemorrhagic fever", "Lujo haemorrhagic fever", "Zambian hemorrhagic fever", "Zambian haemorrhagic fever", "Hemorrhagic fever caused by Lujo virus", "Haemorrhagic fever caused by Lujo virus", "Hemorrhagic fever caused by Lujo virus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lujo hemorrhagic fever", "shortest_name_length": 20}
{"curie": "MONDO:0013502", "names": ["PLCA2", "primary localized cutaneous amyloidosis 2", "amyloidosis, primary localized cutaneous, 2", "AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 2", "amyloidosis, primary localized cutaneous, type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyloidosis, primary localized cutaneous, 2", "shortest_name_length": 5}
{"curie": "UMLS:C3897735", "names": ["Recurrent Malignant Extragonadal Nongerminomatous Germ Cell Tumor", "Recurrent Malignant Extragonadal Non-Seminomatous Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Malignant Extragonadal Nongerminomatous Germ Cell Tumor", "shortest_name_length": 65}
{"curie": "MONDO:0018259", "names": ["didymosis aplasticosebacea", "aplasia cutis congenita-nevus sebaceus syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "didymosis aplasticosebacea", "shortest_name_length": 26}
{"curie": "MONDO:0018890", "names": ["Lyell syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lyell syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C2985230", "names": ["Malignant Peripheral Nerve Sheath Tumor with Mesenchymal Differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Peripheral Nerve Sheath Tumor with Mesenchymal Differentiation", "shortest_name_length": 72}
{"curie": "MONDO:0008835", "names": ["ASTHMA, SHORT STATURE, AND ELEVATED IgA", "asthma, short stature, and elevated IgA", "Asthma, Short Stature, and Elevated IgA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "asthma, short stature, and elevated IgA", "shortest_name_length": 39}
{"curie": "MONDO:0017546", "names": ["congenital vertical talus, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital vertical talus, unilateral", "shortest_name_length": 37}
{"curie": "UMLS:C0856197", "names": ["Criminal Injury", "Injury criminal", "Criminal injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Criminal injury", "shortest_name_length": 15}
{"curie": "UMLS:C0345198", "names": ["Congenital ileal stenosis", "Congenital Ileal Stenosis", "ileum; stenosis, congenital", "stenosis; ileum, congenital", "stenosis of ileum congenital", "Congenital stenosis of ileum", "Congenital ileal stenosis (disorder)", "Congenital stenosis of ileum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital ileal stenosis", "shortest_name_length": 25}
{"curie": "MONDO:0010899", "names": ["ENFL1", "nocturnal frontal lobe epilepsy 1", "EPILEPSY, NOCTURNAL FRONTAL LOBE, 1", "epilepsy, nocturnal frontal lobe, 1", "epilepsy, nocturnal frontal lobe, type 1", "EPILEPSY, NOCTURNAL FRONTAL LOBE, TYPE 1", "Epilepsy, Nocturnal Frontal Lobe, Type 1", "autosomal dominant nocturnal frontal lobe epilepsy 1", "autosomal dominant nocturnal frontal lobe epilepsy type 1", "CHRNA4 autosomal dominant nocturnal frontal lobe epilepsy", "autosomal dominant nocturnal frontal lobe epilepsy caused by mutation in CHRNA4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nocturnal frontal lobe epilepsy 1", "shortest_name_length": 5}
{"curie": "UMLS:C1963951", "names": ["Acute overdose", "Acute overdose (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute overdose", "shortest_name_length": 14}
{"curie": "MONDO:0020654", "names": ["UTUC", "cancer pelvis renal ureter", "renal pelvis and ureter TCC", "Renal Pelvis and Ureter TCC", "TCC of Renal Pelvis and Ureter", "TCC of renal pelvis and ureter", "Upper tract urothelial carcinoma", "TCC of the renal pelvis and ureter", "TCC of the Renal Pelvis and Ureter", "renal pelvis/ureter urothelial carcinoma", "Upper Urinary Tract Urothelial Carcinoma", "Renal Pelvis and Ureter Urothelial Cancer", "Urothelial carcinoma of upper urinary tract", "Renal Pelvis and Ureter Urothelial Carcinoma", "renal pelvis and ureter urothelial carcinoma", "Urothelial Carcinoma of the Upper Urinary Tract", "Renal Pelvis and Ureter Transitional Cell Cancer", "renal pelvis and ureter transitional cell cancer", "Transitional cell carcinoma of upper urinary tract", "urothelial carcinoma of the renal pelvis and ureter", "transitional cell cancer of renal pelvis and ureter", "Renal Pelvis and Ureter Transitional Cell Carcinoma", "Transitional Cell Cancer of Renal Pelvis and Ureter", "Urothelial Carcinoma of the Renal Pelvis and Ureter", "renal pelvis and ureter transitional cell carcinoma", "Transitional cell carcinoma of the pelvis and ureter", "Renal pelvis and ureter transitional cell cancer NOS", "Renal pelvis and ureteric cancer transitional cell NOS", "Renal pelvis and ureteric cancer NOS transitional cell", "Renal pelvis and ureteral cancer transitional cell NOS", "Transitional Cell Carcinoma of Renal Pelvis and Ureter", "transitional cell carcinoma of renal pelvis and ureter", "Transitional cell carcinoma of the upper urinary tract", "Transitional Cell Cancer of the Renal Pelvis and Ureter", "transitional cell cancer of the renal pelvis and ureter", "Transitional cell cancer of the renal pelvis and ureter", "transitional cell carcinoma of the renal pelvis and ureter", "Transitional cell cancer of the renal pelvis and ureter NOS", "Transitional cell carcinoma of upper urinary tract (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal pelvis/ureter urothelial carcinoma", "shortest_name_length": 4}
{"curie": "UMLS:C1334256", "names": ["Benign Acquired Melanosis", "Intraepithelial Melanocytic Hyperplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraepithelial Melanocytic Hyperplasia", "shortest_name_length": 25}
{"curie": "MONDO:0004693", "names": ["CIN III", "grade 3 SIN", "SCC in situ", "Grade 3 SIN", "grade III SIN", "Grade III SIN", "cervix Ca in situ", "Intraepidermal carcinoma", "Intra-epidermal carcinoma", "squamous carcinoma in situ", "Squamous carcinoma in situ", "Squamous Carcinoma in situ", "severe dysplasia of cervix", "Squamous Carcinoma In situ", "carcinoma in situ of cervix", "Epidermoid carcinoma in situ", "CIN III - severe dyskaryosis", "Epidermoid carcinoma in-situ", "Epidermoid Carcinoma In situ", "epidermoid carcinoma in situ", "Epidermoid Carcinoma in situ", "Intraepidermal carcinoma, NOS", "IEC - intraepidermal carcinoma", "IEC - Intraepidermal carcinoma", "Squamous cell carcinoma in-situ", "in situ squamous cell carcinoma", "Stage 0 Squamous Cell Carcinoma", "carcinoma squamous cell in situ", "Squamous Cell Carcinoma In situ", "squamous cell carcinoma in situ", "Squamous Cell Carcinoma in situ", "stage 0 squamous cell carcinoma", "squamous cell carcinoma in-situ", "Squamous cell carcinoma in situ", "Squamous Cell Carcinoma in-situ", "stage 0 uterine cervix carcinoma", "uterine cervix in situ carcinoma", "Epidermoid carcinoma in situ, NOS", "Epidermoid Cell Carcinoma In situ", "epidermoid cell carcinoma in situ", "Epidermoid Cell Carcinoma in situ", "carcinoma in situ of uterine cervix", "Squamous cell carcinoma in situ NOS", "severe dysplasia of the cervix uteri", "Squamous cell carcinoma in situ, NOS", "CIN III - carcinoma in situ of cervix", "[M]Squamous cell carcinoma in situ NOS", "Intraepithelial squamous cell carcinoma", "Intraepithelial Squamous Cell Carcinoma", "intraepithelial squamous cell carcinoma", "Grade 3 Squamous Intraepithelial Neoplasia", "Squamous cell carcinoma in situ (disorder)", "High grade squamous intraepithelial lesion", "grade 3 squamous intraepithelial neoplasia", "squamous cell carcinoma in situ (diagnosis)", "carcinoma, squamous cell, in situ, malignant", "CARCINOMA, SQUAMOUS CELL, IN SITU, MALIGNANT", "grade III squamous intraepithelial neoplasia", "Grade III Squamous Intraepithelial Neoplasia", "Squamous intraepithelial neoplasia, grade III", "squamous intraepithelial neoplasia, grade III", "Squamous intraepithelial neoplasia, high grade", "Intraepithelial squamous cell carcinoma (disorder)", "Squamous cell carcinoma in situ (morphologic abnormality)", "cervical intraepithelial neoplasia grade III with severe dysplasia", "Squamous intraepithelial neoplasia, grade III (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "squamous carcinoma in situ", "shortest_name_length": 7}
{"curie": "UMLS:C1262113", "names": ["Lipohypertrophy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lipohypertrophy", "shortest_name_length": 15}
{"curie": "MONDO:0002871", "names": ["testicular trophoblastic tumor", "Testicular Trophoblastic Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "testicular trophoblastic tumor", "shortest_name_length": 30}
{"curie": "UMLS:C1335990", "names": ["Small Intestinal Atypical Burkitt/Burkitt-Like Lymphoma", "Small Intestine Atypical Burkitt's/Burkitt's-like Lymphoma", "Primary Small Intestinal Atypical Burkitt's/Burkitt's-Like Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Intestinal Atypical Burkitt/Burkitt-Like Lymphoma", "shortest_name_length": 55}
{"curie": "UMLS:C0267509", "names": ["Chronic idiopathic constipation", "constipation chronic idiopathic", "Chronic idiopathic constipation (disorder)", "Chronic idiopathic constipation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic idiopathic constipation", "shortest_name_length": 31}
{"curie": "UMLS:C0677984", "names": ["regional cancer", "Locally advanced", "Locally Advanced Cancer", "locally advanced cancer", "Locally advanced cancer", "Locally advanced malignant tumor", "Locally advanced malignant tumour", "Locally Advanced Malignant Neoplasm", "Locally advanced malignant neoplasm", "Locally Metastatic Malignant Neoplasm", "Locally advanced malignant neoplasm (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Malignant Neoplasm", "shortest_name_length": 15}
{"curie": "MONDO:0023250", "names": ["global disaccharide intolerance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "global disaccharide intolerance", "shortest_name_length": 31}
{"curie": "MONDO:0021354", "names": ["Fatty neoplasm", "Lipomatous Tumor", "lipomatous tumor", "Lipomatous tumor", "Lipomatous tumour", "Adipocytic neoplasm", "Lipomatous neoplasm", "lipomatous neoplasm", "Lipomatous Neoplasm", "LIPOMATOUS NEOPLASMS", "adipose tissue tumor", "Lipomatous Neoplasms", "Adipose Tissue Tumor", "adipose tissue neoplasm", "Adipose Tissue Neoplasm", "Tumor of adipose tissue", "Adipose tissues--Tumors", "Tumor of Adipose Tissue", "tumor of adipose tissue", "Neoplasm, Adipose Tissue", "Tumour of adipose tissue", "Adipose Tissue Neoplasms", "Neoplasms, Adipose Tissue", "Neoplasm of Adipose Tissue", "neoplasm of adipose tissue", "Lipomatous tumor (disorder)", "Tumor of the Adipose Tissue", "tumor of the adipose tissue", "lipomatous tumor (diagnosis)", "neoplasm of the adipose tissue", "Neoplasm of the Adipose Tissue", "adipose tissue neoplasm (disease)", "Tumor of adipose tissue (disorder)", "neoplasm of adipose tissue (diagnosis)", "Soft tissue tumor of adipose differentiation", "Soft tissue tumour of adipose differentiation", "Lipomatous neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tumor of adipose tissue", "shortest_name_length": 14}
{"curie": "UMLS:C0392473", "names": ["Abdominal aorta thrombosis", "Abdominal Aorta Thrombosis", "Abdominal Aortic Thrombosis", "THROMBOSIS, AORTA, ABDOMINAL", "aorta; thrombosis, abdominal", "thrombosis; aortic, abdominal", "Thrombosis of abdominal aorta", "thrombosis of abdominal aorta", "Thrombosis of abdominal aorta (disorder)", "thrombosis of abdominal aorta (diagnosis)", "aortic artery thrombosis of abdominal aorta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thrombosis of abdominal aorta", "shortest_name_length": 26}
{"curie": "MONDO:0017610", "names": ["EBS", "EEB", "epidermolysis bullosa simplex", "Epidermolysis Bullosa Simplex", "Epidermolysis bullosa simplex", "epidermolysis; bullosa, simplex", "Epidermolysis Bullosa Simplices", "Bullosa Simplices, Epidermolysis", "epidermolysis bullosa intraepidermic", "Epidermolysis bullosa simplex (disorder)", "epidermolysis bullosa simplex (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolysis bullosa simplex", "shortest_name_length": 3}
{"curie": "UMLS:C4521641", "names": ["Stage IIB Esophageal Adenocarcinoma", "Clinical Stage IIB Esophageal Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage IIB Esophageal Adenocarcinoma AJCC v8", "shortest_name_length": 35}
{"curie": "MONDO:0011875", "names": ["EJM8", "EJA2", "EIG11", "CLCN2 generalised epilepsy", "idiopathic generalized epilepsy 11", "EPILEPSY, JUVENILE ABSENCE, SUSCEPTIBILITY TO, 2", "generalised epilepsy caused by mutation in CLCN2", "epilepsy, juvenile absence, susceptibility to, 2", "EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 8", "epilepsy, juvenile myoclonic, susceptibility to, 8", "susceptibility to idiopathic generalized epilepsy 11", "epilepsy, idiopathic generalized, susceptibility to, 11", "EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 11", "epilepsy, idiopathic generalized, susceptibility to, type 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epilepsy, idiopathic generalized, susceptibility to, 11", "shortest_name_length": 4}
{"curie": "UMLS:C4281603", "names": ["LUMBAR SPINAL CORD INJURY", "spinal cord injury lumbar", "Lumbar Spinal Cord Injury", "Spinal cord injury lumbar", "injury; spinal cord, lumbar", "Injury of lumbar spinal cord", "injury of lumbar spinal cord", "Injury of lumbar spinal cord (disorder)", "injury of lumbar spinal cord (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of lumbar spinal cord", "shortest_name_length": 25}
{"curie": "MONDO:0001235", "names": ["Appendix cancer", "Appendix Cancer", "appendix cancer", "cancer appendix", "Cancer, Appendix", "appendiceal cancer", "cancer of appendix", "Appendiceal cancer", "Cancer of Appendix", "Appendiceal Cancer", "Cancer, Appendiceal", "Cancer of the Appendix", "cancer of the appendix", "Malignant Appendix Tumor", "appendix tumor malignant", "malignant appendix tumor", "vermiform appendix cancer", "Malignant Tumor of Appendix", "Malignant tumor of appendix", "malignant appendix neoplasm", "Malignant Appendix Neoplasm", "malignant tumor of appendix", "cancer of vermiform appendix", "Malignant tumour of appendix", "malignant appendiceal neoplasm", "Malignant neoplasm of appendix", "Malignant Neoplasm of Appendix", "malignant neoplasm of appendix", "malignant tumor of the appendix", "Malignant Tumor of the Appendix", "malignant neoplasm of the appendix", "Malignant Neoplasm of the Appendix", "malignant vermiform appendix neoplasm", "malignant neoplasm of vermiform appendix", "Malignant neoplasm of appendix (disorder)", "Malignant Neoplasm of Appendix Vermiformis", "malignant neoplasm of appendix (diagnosis)", "Malignant neoplasm of appendix vermiformis", "malignant neoplasm of appendix vermiformis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "appendix cancer", "shortest_name_length": 15}
{"curie": "MONDO:0100156", "names": ["MGA1", "Mga1", "IGS1", "MGA-1", "Imerslund disease", "Imerslund's syndrome", "Megaloblastic Anemia 1", "MEGALOBLASTIC ANEMIA, 1", "megaloblastic anemia, 1", "Imerslund-Grasbeck anemia", "Imerslund-Grasbeck anaemia", "Imerslund-Grasbeck disease", "Imerslund-Grasbeck syndrome", "Imerslund-Gräsbeck Syndrome", "megaloblastic Anemia type 1", "Imerslund-Gräsbeck syndrome", "Imerslund-Grasbeck Syndrome", "Imerslund-Graesbeck syndrome", "Imerslund-Grasbeck syndrome 1", "IMERSLUND-GRASBECK SYNDROME 1", "Juvenile Megaloblastic Anemia", "Imerslund (Gräsbeck) syndrome", "Familial megaloblastic anemia", "Congenital vitamin B12 deficiency", "MEGALOBLASTIC ANEMIA, FINNISH TYPE", "Enterocyte cobalamin malabsorption", "megaloblastic anemia, Finnish type", "Imerslund-Grasbeck syndrome type 1", "enterocyte cobalamin malabsorption", "Imerslund-Najman-Grasbeck syndrome", "ENTEROCYTE COBALAMIN MALABSORPTION", "Imerslund-Grasbeck Syndrome (diagnosis)", "Selective malabsorption of cyanocobalamin", "ENTEROCYTE INTRINSIC FACTOR RECEPTOR, DEFECT OF", "Enterocyte intrinsic factor receptor, defect of", "enterocyte intrinsic factor receptor, defect of", "Selective cobalamin malabsorption with proteinuria", "Selective malabsorption of cyanocobalamin (disorder)", "Vitamin B12 deficiency anemia due to selective malabsorption of cyanocobalamin", "Vitamin B12 deficiency anaemia due to selective malabsorption of cyanocobalamin", "pernicious anemia, juvenile, due to selective intestinal malabsorption of vitamin b12, with proteinuria", "PERNICIOUS ANEMIA, JUVENILE, DUE TO SELECTIVE INTESTINAL MALABSORPTION OF VITAMIN B12, WITH PROTEINURIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Imerslund-Grasbeck syndrome type 1", "shortest_name_length": 4}
{"curie": "MONDO:0010604", "names": ["HEMB", "hem B", "HEMOPHILIA B", "hemophilia b", "Hemophilia B", "hemophilia B", "b hemophilia", "Hemophilia Bs", "b haemophilia", "haemophilia b", "B; hemophilia", "F9 Deficiency", "Haemophilia B", "F9 deficiency", "hemophilia; B", "F9 DEFICIENCY", "Haemophilia Bs", "Deficiency, F9", "Bs, Hemophilia", "PTC DEFICIENCY", "Hemophilia B(M)", "Deficiency, PTC", "hemophilia B(M)", "HEMOPHILIA B(M)", "PTC; deficiency", "deficiency; PTC", "F9 Deficiencies", "Deficiencies, F9", "christmas disease", "Hemophilia B, NOS", "Hemophilia Bs (M)", "Christmas disease", "hemophilia type B", "CHRISTMAS DISEASE", "Christmas Disease", "disease; Christmas", "Haemophilia B, NOS", "Disease, Christmas", "Christmas; disease", "hemophilia B Leyden", "HEMOPHILIA B LEYDEN", "Hemophilia B Leyden", "factor 9 deficiency", "FACTOR IX DEFICIENCY", "factor IX deficiency", "factor ix deficiency", "Factor IX Deficiency", "Factor IX deficiency", "Deficiency, factor IX", "Deficiency, Factor IX", "PTC deficiency disease", "Factor IX Deficiencies", "Deficiencies, Factor IX", "hemophilia B (diagnosis)", "Hemophilia B (Factor IX)", "Congenital F9 deficiency", "Haemophilia B (Factor IX)", "F9 deficiency, Leyden type", "AUTOPROTHROMBIN II DEFICIENCY", "Christmas disease (Factor IX)", "Congenital factor IX disorder", "congenital factor IX disorder", "Factor IX deficiency (disorder)", "Congenital factor IX deficiency", "Hereditary factor IX deficiency", "Hereditary Factor IX Deficiency", "congenital factor IX deficiency", "hereditary Factor IX deficiency", "Deficiency, functional factor IX", "disease (or disorder); Christmas", "factor IX deficiency (diagnosis)", "hemophilia b, X-linked recessive", "deficiency, functional factor IX", "Factor IX deficiency, Leyden type", "ANTIHEMOPHILIC FACTOR B DEFICIENCY", "factor IX deficiency (hemophilia B)", "Hereditary Factor IX Deficiency Disease", "Hereditary factor IX deficiency disease", "hereditary Factor IX deficiency disease", "Sex-linked factor IX deficiency disease", "plasma thromboplastin component deficiency", "PLASMA THROMBOPLASTIN COMPONENT DEFICIENCY", "Plasma Thromboplastin Component Deficiency", "Deficiency, plasma thromboplastin component", "plasma thromboplastin; component, deficiency", "Plasma thromboplastin component [PTC] deficiency", "deficiency; PTC (plasma thromboplastin component)", "deficiency; plasma thromboplastin component (PTC)", "Hereditary factor IX deficiency disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemophilia B", "shortest_name_length": 4}
{"curie": "UMLS:C0740447", "names": ["NEUROPATHY DIABETIC PERIPHERAL", "diabetic neuropathy peripheral", "Diabetic peripheral neuropathy", "diabetic peripheral neuropathy", "peripheral diabetic neuropathy", "diabetic peripheral neuropathy (diagnosis)", "Peripheral neuropathy due to diabetes mellitus", "Peripheral neuropathy due to diabetes mellitus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diabetic peripheral neuropathy", "shortest_name_length": 30}
{"curie": "UMLS:C0751097", "names": ["Secondary Empty Sella Syndrome", "Empty Sella Syndrome, Secondary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Empty Sella Syndrome, Secondary", "shortest_name_length": 30}
{"curie": "MONDO:0013683", "names": ["VUR5", "vesicoureteral reflux 5", "VESICOURETERAL REFLUX 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vesicoureteral reflux 5", "shortest_name_length": 4}
{"curie": "MONDO:0024813", "names": ["Pulmonary Sulcus Tumor", "pulmonary sulcus tumor", "pulmonary sulcus neoplasm", "Pulmonary Sulcus Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary sulcus neoplasm", "shortest_name_length": 22}
{"curie": "MONDO:0011658", "names": ["PARK7", "Parkinson's disease 7", "PARK7 Parkinson disease", "Parkinson disease caused by mutation in PARK7", "autosomal recessive early-onset Parkinson disease 7", "Parkinson Disease 7, Autosomal Recessive Early-Onset", "PARKINSON DISEASE 7, AUTOSOMAL RECESSIVE EARLY-ONSET", "Parkinson disease 7, autosomal recessive early-onset", "autosomal recessive early-onset Parkinson's disease 7", "autosomal recessive early-onset Parkinson disease type 7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive early-onset Parkinson disease 7", "shortest_name_length": 5}
{"curie": "MONDO:0002542", "names": ["Spinal Cord Glioma", "spinal cord glioma", "glioma of spinal cord", "Glioma of spinal cord", "spinal cord glial tumor", "Spinal Cord Glial Tumor", "Glial Neoplasm Spinal Cord", "Spinal Cord Glial Neoplasm", "glial neoplasm spinal cord", "spinal cord glial neoplasm", "Glial neoplasm Spinal Cord", "Glial Tumor of Spinal Cord", "glial tumor of spinal cord", "Glial tumor of spinal cord", "Glial tumour of spinal cord", "spinal cord malignant glioma", "neoplasm - spinal cord glial", "neoplasm - spinal cord glioma", "malignant glioma of spinal cord", "Glioma of spinal cord (disorder)", "Glioma of spinal cord (diagnosis)", "Glial tumor of spinal cord (disorder)", "Glial tumor of spinal cord (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal cord glioma", "shortest_name_length": 18}
{"curie": "MONDO:0044937", "names": ["Rectum Cancer", "Rectal Cancer", "rectum cancer", "rectal cancer", "Rectal cancer", "Rectum Cancers", "rectal cancers", "Rectum--Cancer", "Cancer, Rectum", "Rectal Cancers", "Cancer, Rectal", "Rectal carcinoma", "Rectal Carcinoma", "Carcinoma;rectum", "rectum carcinoma", "cancer of rectum", "RECTAL CARCINOMA", "Carcinoma rectum", "rectal carcinoma", "CARCINOMA RECTUM", "Cancer of Rectum", "Rectal cancer NOS", "rectum; carcinoma", "Carcinoma of rectum", "carcinoma of rectum", "CARCINOMA OF RECTUM", "Carcinoma of Rectum", "cancer of the rectum", "Cancer of the Rectum", "CA - Cancer of rectum", "carcinoma of the rectum", "Carcinoma of the Rectum", "malignant neoplasm of rectum", "carcinoma of rectum (diagnosis)", "rectal neoplasm malignant carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rectal carcinoma", "shortest_name_length": 13}
{"curie": "MONDO:0006188", "names": ["EBV-Positive T-Cell Lymphoproliferative Disease of Childhood", "EBV-positive T-cell lymphoproliferative disease of childhood", "EBV-positive T-cell lymphoproliferative disorder of childhood", "EBV-Positive T-Cell Lymphoproliferative Disorder of Childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "EBV-positive T-cell lymphoproliferative disorder of childhood", "shortest_name_length": 60}
{"curie": "MONDO:0019766", "names": ["X-linked intellectual disability, Porteous type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked intellectual disability, Porteous type", "shortest_name_length": 47}
{"curie": "UMLS:C4745241", "names": ["Refractory Hormone Receptor Positive Breast Carcinoma", "Refractory Hormone Receptor-Positive Breast Carcinoma", "Refractory Hormone Receptor Positive Breast Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Hormone Receptor-Positive Breast Carcinoma", "shortest_name_length": 53}
{"curie": "MONDO:0017862", "names": ["paraquat poisoning"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "paraquat poisoning", "shortest_name_length": 18}
{"curie": "MONDO:0005761", "names": ["Wuchereriasis", "Elephantiasis", "elephantiasis", "Lymphatic filariasis", "Lymphatic Filariasis", "filariasis lymphatic", "Filariasis lymphatic", "lymphatic filariasis", "Lymphatic Filariases", "eyelid elephantiasis", "Filariases, Lymphatic", "Filariasis, Lymphatic", "eyelid; elephantiasis", "elephantiasis; eyelid", "Bancroftian filariasis", "Filarial Elephantiases", "filarial elephantiasis", "Filarial Elephantiasis", "Filarial elephantiasis", "Elephantiasis of eyelid", "Elephantiasis, Filarial", "ELEPHANTIASIS, FILARIAL", "elephantiasis; filarial", "Elephantiases, Filarial", "elephantiasis of eyelid", "filarial; elephantiasis", "Bancroftian elephantiasis", "Malayi tropical eosinphilia", "Bancroftian filarial chyluria", "eyelid disorder elephantiasis", "Wuchereria Bancrofti infection", "Lymphatic filariasis (disorder)", "lymphatic filariasis (diagnosis)", "Elephantiasis of eyelid (disorder)", "elephantiasis of eyelid (diagnosis)", "elephantiasis of eyelid (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "filarial elephantiasis", "shortest_name_length": 13}
{"curie": "MONDO:0015583", "names": ["Del(2)(p21)", "monosomy 2p21", "Monosomy 2p21", "2p21 deletion syndrome", "2p21 Microdeletion Syndrome", "2p21 microdeletion syndrome", "2p21 microdeletion syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "2p21 microdeletion syndrome", "shortest_name_length": 11}
{"curie": "MONDO:0004086", "names": ["ciliary body epithelioid cell melanoma", "Ciliary Body Epithelioid Cell Melanoma", "Epithelioid Cell Melanoma of Ciliary Body", "epithelioid cell melanoma of ciliary body", "epithelioid cell melanoma of the ciliary body", "Epithelioid Cell Melanoma of the Ciliary Body"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ciliary body epithelioid cell melanoma", "shortest_name_length": 38}
{"curie": "UMLS:C4525204", "names": ["IIIA", "Stage IIIA Hepatocellular Cancer", "Stage IIIA Liver Cell Carcinoma AJCC v8", "Stage IIIA Hepatocellular Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Hepatocellular Carcinoma AJCC v8", "shortest_name_length": 4}
{"curie": "UMLS:C4054727", "names": ["Infant ALL", "Infant Acute Lymphoblastic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infant Acute Lymphoblastic Leukemia", "shortest_name_length": 10}
{"curie": "MONDO:0045015", "names": ["carbohydrate transport disease", "Carbohydrate transport disorder", "disorder of carbohydrate transport", "Disorder of carbohydrate transport", "DISORDERS OF CARBOHYDRATE TRANSPORT", "Disorder of carbohydrate transport, NOS", "Disorder of carbohydrate transport (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carbohydrate transport disease", "shortest_name_length": 30}
{"curie": "MONDO:0014523", "names": ["ACPHD", "Combined cerebellar and peripheral ataxia-deafness-diabetes mellitus syndrome", "Combined cerebellar and peripheral ataxia, deafness, diabetes mellitus syndrome", "combined cerebellar and peripheral ataxia-hearing loss-diabetes mellitus syndrome", "Combined cerebellar and peripheral ataxia-hearing loss-diabetes mellitus syndrome", "juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome", "Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome", "Juvenile-onset diabetes mellitus, central and peripheral neurodegeneration syndrome", "ATAXIA, COMBINED CEREBELLAR AND PERIPHERAL, WITH HEARING LOSS AND DIABETES MELLITUS", "ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus", "Combined cerebellar and peripheral ataxia, hearing loss, diabetes mellitus syndrome", "Juvenile-onset diabetes mellitus, central and peripheral neurodegeneration syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0002437", "names": ["Dehydration polycythemia", "Dehydration Polycythemia", "dehydration polycythemia", "Dehydration polycythaemia", "polycythemia; fall in plasma volume", "fall in plasma volume; polycythemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dehydration polycythemia", "shortest_name_length": 24}
{"curie": "UMLS:C0521481", "names": ["mucosal edema", "edema mucosal", "Mucosal edema", "Edema mucosal", "Mucosal oedema", "Oedema mucosal", "Edema mucosal NOS", "Mucosal edema NOS", "Oedema mucosal NOS", "Mucosal oedema NOS", "Mucous membrane edema", "Mucous membrane oedema", "Mucous membrane edema (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mucous membrane edema", "shortest_name_length": 13}
{"curie": "UMLS:C0574143", "names": ["hepatolith", "Hepatolith", "Liver calculus", "calculus; liver", "liver; calculus", "Hepatolithiasis", "Liver calculus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liver calculus", "shortest_name_length": 10}
{"curie": "MONDO:0004221", "names": ["uterine corpus PEComa", "Uterine Corpus PEComa", "uterus perivascular epithelioid cell tumor", "uterine perivascular epithelioid cell tumor", "uterine corpus perivascular epithelioid cell tumor", "Uterine Corpus Perivascular Epithelioid Cell Tumor", "body of uterus neoplasm with perivascular epithelioid cell differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine corpus perivascular epithelioid cell tumor", "shortest_name_length": 21}
{"curie": "UMLS:C5418767", "names": ["Recurrent Platinum-Resistant Ovarian Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Platinum-Resistant Ovarian Carcinoma", "shortest_name_length": 46}
{"curie": "MONDO:0012421", "names": ["DFNB44", "autosomal recessive deafness 44", "deafness, autosomal recessive 44", "DEAFNESS, AUTOSOMAL RECESSIVE 44", "Deafness, Autosomal Recessive 44", "deafness, autosomal recessive type 44", "autosomal recessive nonsyndromic deafness 44", "ADCY1 autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 44", "autosomal recessive nonsyndromic deafness type 44", "autosomal recessive nonsyndromic deafness caused by mutation in ADCY1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 44", "shortest_name_length": 6}
{"curie": "UMLS:C5420354", "names": ["Parotid Gland Follicular Lymphoma", "Primary Parotid Gland Follicular Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parotid Gland Follicular Lymphoma", "shortest_name_length": 33}
{"curie": "UMLS:C0751012", "names": ["anterior choroidal artery stroke", "stroke of anterior choroidal artery", "Anterior Choroidal Artery Infarction", "stroke of anterior choroidal artery (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anterior Choroidal Artery Infarction", "shortest_name_length": 32}
{"curie": "MONDO:0002496", "names": ["Submucosal Invasive Colon Adenocarcinoma", "submucosal invasive colon adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "submucosal invasive colon adenocarcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0012715", "names": ["MGR12", "MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 12", "migraine with or without aura, susceptibility to, 12", "migraine, with or without aura, susceptibility to, 12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "migraine with or without aura, susceptibility to, 12", "shortest_name_length": 5}
{"curie": "UMLS:C4525735", "names": ["Colorectal Neuroendocrine Tumor by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Neuroendocrine Tumor by AJCC v8 Stage", "shortest_name_length": 48}
{"curie": "UMLS:C0751042", "names": ["inherited color blindness", "Inherited Color Blindness", "blindness color inherited", "blindness color inheriting", "Color Blindness, Inherited"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Color Blindness, Inherited", "shortest_name_length": 25}
{"curie": "UMLS:C0024950", "names": ["Maxillary Disease", "Disease, Maxillary", "Maxillary Diseases", "Maxillary Disorders", "Diseases, Maxillary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Maxillary Diseases", "shortest_name_length": 17}
{"curie": "UMLS:C0178824", "names": ["Reactive Hyperemia", "hyperemia reactive", "reactive hyperemia", "Reactive Hyperemias", "Hyperemia, Reactive", "Hyperemias, Reactive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Reactive Hyperemia", "shortest_name_length": 18}
{"curie": "MONDO:0010323", "names": ["ATKIN SYNDROME", "Atkin syndrome", "Atkin Flaitz syndrome", "Atkin-Flaitz syndrome", "ATKIN-FLAITZ SYNDROME", "Atkin-Flaitz-Patil syndrome", "Atkin Flaitz Patil Smith syndrome", "Mental retardation X-linked Atkin type", "Mental retardation X-linked, Atkin type", "Mental retardation, X-linked, nonspecific", "X-linked intellectual disability Atkin type", "X-linked intellectual disability, Atkin type", "X-linked mental retardation syndrome, Atkin type", "Mental retardation, X-linked nonspecific, type 1", "X-linked intellectual disability Atkin type (disorder)", "X-linked intellectual disability Atkin type (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atkin-Flaitz syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C4763961", "names": ["Sexually Transmitted Chlamydial Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sexually Transmitted Chlamydial Disease", "shortest_name_length": 39}
{"curie": "MONDO:0005524", "names": ["sweat gland carcinoma", "Sweat Gland Carcinoma", "Sweat gland carcinoma", "carcinoma of sweat gland", "Carcinoma of Sweat Gland", "Malignant sweat gland tumor", "carcinoma of the Sweat gland", "Carcinoma of the Sweat Gland", "carcinoma of the sweat gland", "Malignant sweat gland tumour", "CARCINOMA, SWEAT GLAND, MALIGNANT", "carcinoma, sweat gland, malignant", "sweat gland carcinoma/apocrine eccrine carcinoma", "Malignant skin tumor with eccrine differentiation", "Malignant skin tumour with eccrine differentiation", "malignant skin neoplasm with eccrine differentiation", "skin neoplasm malignant adnexa with eccrine differentiation", "Malignant skin tumor with eccrine differentiation (disorder)", "malignant skin neoplasm with eccrine differentiation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sweat gland carcinoma", "shortest_name_length": 21}
{"curie": "MONDO:0030919", "names": ["MRD53", "autosomal dominant mental retardation 53", "mental retardation, autosomal dominant 53", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 53", "autosomal dominant intellectual disability 53", "intellectual disability, autosomal dominant 53", "autosomal dominant intellectual developmental disorder 53", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 53"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 53", "shortest_name_length": 5}
{"curie": "MONDO:0014816", "names": ["SFMMP", "split-foot malformation with mesoaxial polydactyly", "SPLIT-FOOT MALFORMATION WITH MESOAXIAL POLYDACTYLY", "Split-foot malformation-mesoaxial polydactyly syndrome", "split-foot malformation-mesoaxial polydactyly syndrome", "Split-foot malformation, mesoaxial polydactyly syndrome", "SFMMP (split-foot malformation, mesoaxial polydactyly) syndrome", "Split-foot malformation, mesoaxial polydactyly syndrome (disorder)", "split-foot malformation-mesoaxial polydactyly-nail abnormalities-sensorineural hearing loss syndrome", "Split-foot malformation-mesoaxial polydactyly-nail abnormalities-sensorineural hearing loss syndrome", "Split-foot malformation, mesoaxial polydactyly, nail abnormalities, sensorineural hearing loss syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "split-foot malformation-mesoaxial polydactyly syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0010967", "names": ["Dfnb7", "DFNB7", "DFNB11", "autosomal recessive deafness 7", "Deafness, Autosomal Recessive 7", "DEAFNESS, AUTOSOMAL RECESSIVE 7", "deafness, autosomal recessive 7", "DEAFNESS, AUTOSOMAL RECESSIVE 11", "deafness, autosomal recessive 11", "Deafness, Autosomal Recessive 11", "deafness, autosomal recessive type 7", "autosomal recessive nonsyndromic deafness 7", "TMC1 autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 7", "autosomal recessive nonsyndromic deafness type 7", "autosomal recessive nonsyndromic deafness caused by mutation in TMC1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 7", "shortest_name_length": 5}
{"curie": "MONDO:0012736", "names": ["LQT9", "LQT2/9, DIGENIC", "LQT9 (diagnosis)", "Long Qt Syndrome 9", "LONG QT SYNDROME 9", "long QT syndrome 9", "Long Qt Syndrome 2-9", "CAV3 long QT syndrome", "long QT syndrome type 9", "long QT syndrome 2/9, digenic", "LONG QT SYNDROME 2/9, DIGENIC", "long QT syndrome caused by mutation in CAV3", "LONG QT SYNDROME 9, ACQUIRED, SUSCEPTIBILITY TO", "long QT syndrome 9, acquired, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "long QT syndrome 9", "shortest_name_length": 4}
{"curie": "MONDO:0010317", "names": ["MRX54", "MRX87", "MRX52", "MRX29", "Mrx76", "MRX38", "Mrx38", "MRX33", "Mrx54", "MRX32", "Mrx43", "MRX43", "Mrx29", "Mrx87", "MRX76", "Mrx32", "Mrx33", "MRXARX", "XLID29", "X-linked mental retardation 54", "X-linked mental retardation 43", "X-linked mental retardation 87", "X-linked mental retardation 33", "X-linked mental retardation 32", "X-linked mental retardation 38", "X-linked mental retardation 76", "X-linked mental retardation 36", "X-linked mental retardation 52", "X-linked mental retardation 29", "mental retardation, X-linked 29", "MENTAL RETARDATION, X-LINKED 54", "MENTAL RETARDATION, X-LINKED 76", "MENTAL RETARDATION, X-LINKED 29", "mental retardation, X-linked 43", "Mental Retardation, X-Linked 33", "Mental Retardation, X-Linked 87", "Mental Retardation, X-Linked 76", "mental retardation, X-linked 32", "Mental Retardation, X-Linked 32", "MENTAL RETARDATION, X-LINKED 33", "Mental Retardation, X-Linked 43", "Mental Retardation, X-Linked 52", "mental retardation, X-linked 87", "MENTAL RETARDATION, X-LINKED 87", "mental retardation, X-linked 76", "Mental Retardation, X-Linked 38", "mental retardation, X-linked 33", "MENTAL RETARDATION, X-LINKED 43", "mental retardation, X-linked 38", "Mental Retardation, X-Linked 54", "MENTAL RETARDATION, X-LINKED 32", "MENTAL RETARDATION, X-LINKED 38", "Mental Retardation, X-Linked 29", "MENTAL RETARDATION, X-LINKED 52", "mental retardation, X-linked 54", "mental retardation, X-linked 52", "ARX-related intellectual disability", "intellectual disability, X-linked 32", "intellectual disability, X-linked 38", "intellectual disability, X-linked 33", "intellectual disability, X-linked 52", "intellectual disability, X-linked 43", "intellectual disability, X-linked 76", "intellectual disability, X-linked 29", "intellectual disability, X-linked 87", "intellectual disability, X-linked 54", "X-linked mental retardation 29 and others", "X-linked mental retardation 32 (MRX32, XLMR32)", "X-linked mental retardation 29 (MRX29, XLMR29)", "X-linked mental retardation 38 (MRX38, XLMR38)", "X-linked mental retardation 36 (MRX36, XLMR36)", "X-linked mental retardation 33 (MRX33, XLMR33)", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 29", "non-syndromic X-linked intellectual disability ARX-related", "X-linked mental retardation with or without seizures ARX-related", "mental retardation, X-linked, with or without seizures, arx-RELATED", "Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related", "mental retardation, X-linked, with or without seizures, arx-related", "intellectual developmental disorder, X-linked 29, X-linked recessive", "intellectual disability, X-linked, with or without seizures, arx-related", "intellectual disability, X-linked, with or without seizures, ARX-related", "intellectual disability, X-linked, with or without seizures, arx-RELATED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked, with or without seizures, arx-related", "shortest_name_length": 5}
{"curie": "UMLS:C5555530", "names": ["Refractory Ovarian Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Ovarian Squamous Cell Carcinoma", "shortest_name_length": 42}
{"curie": "UMLS:C1511265", "names": ["Borderline Ovarian Mucinous Tumor, Intestinal Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Ovarian Mucinous Tumor, Intestinal Type", "shortest_name_length": 50}
{"curie": "MONDO:0015722", "names": ["vitamin K-dependent clotting factors, combined deficiency of", "congenital vitamin K-dependent coagulation factors deficiency", "congenital vitamin K-dependent coagulation factors combined deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital vitamin K-dependent coagulation factors deficiency", "shortest_name_length": 60}
{"curie": "MONDO:0021539", "names": ["skin appendage hamartoma", "Skin Appendage Hamartoma", "Hamartoma of skin appendage", "Hamartoma of Skin Appendage", "hamartoma of skin appendage", "Hamartoma of skin appendage (disorder)", "cutaneous appendage hamartoma (disease)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hamartoma of skin appendage", "shortest_name_length": 24}
{"curie": "MONDO:0016843", "names": ["Del(20)(q13.33)", "Monosomy 20q13.33", "monosomy 20q13.33", "20q13.33 microdeletion syndrome", "20q13.33 microdeletion syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "20q13.33 microdeletion syndrome", "shortest_name_length": 15}
{"curie": "UMLS:C5419561", "names": ["Locally Advanced Renal Pelvis Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Renal Pelvis Carcinoma", "shortest_name_length": 39}
{"curie": "UMLS:C4525262", "names": ["Stage II Intrahepatic Bile Duct Cancer", "Stage II Intrahepatic Bile Duct Cancer AJCC v8", "Stage II Intrahepatic Bile Duct Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Intrahepatic Bile Duct Cancer AJCC v8", "shortest_name_length": 38}
{"curie": "UMLS:C0016169", "names": ["Sinus", "FISTULA", "Fistula", "fistula", "Sinuses", "fistulas", "Fistulas", "XXX>Fistula", "Fistula NOS", "Fistula, NOS", "fistulous tract", "Fistulous tract", "fistula (___ cm)", "pathologic fistula", "Pathologic Fistula", "Fistula (disorder)", "Fistulous tract, NOS", "Abnormal sinus tract", "Abnormal sinus tract, NOS", "fistula (physical finding)", "Sinus (morphologic abnormality)", "Fistula (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pathologic fistula", "shortest_name_length": 5}
{"curie": "MONDO:0003069", "names": ["lymphadenitis; purulent", "purulent; lymphadenitis", "Lymphadenitis suppurative", "Suppurative lymphadenitis", "suppurative lymphadenitis", "Suppurative Lymphadenitis", "lymphadenitis; suppurative", "suppurative; lymphadenitis", "Suppurative lymphadenopathy", "suppurative lymphadenopathy", "lymphadenopathy suppurative", "Lymphadenopathy suppurative", "LYMPHADENOPATHY SUPPURATIVE", "Suppurative lymphadenopathy (disorder)", "Suppurative lymphadenopathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "suppurative lymphadenitis", "shortest_name_length": 23}
{"curie": "MONDO:0030711", "names": ["CDAN3B", "CDA, IIA IIIB", "CDA, TYPE IIIb", "anemia, congenital dyserythropoietic, IIA IIIB, autosomal recessive", "Anemia, congenital dyserythropoietic, type IIIb, autosomal recessive", "ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IIIb, AUTOSOMAL RECESSIVE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anemia, congenital dyserythropoietic, type IIIb, autosomal recessive", "shortest_name_length": 6}
{"curie": "MONDO:0005262", "names": ["CNS Cyst", "CNS cyst", "Cyst, CNS", "CNS Cysts", "Cysts, CNS", "Cyst of CNS", "cyst of CNS", "cyst of the CNS", "Cyst of the CNS", "suprasellar cyst", "suprasellar cysts", "cyst, suprasellar", "cysts, suprasellar", "Rathke cleft cysts", "cysts, Rathke cleft", "Rathkes cleft cysts", "Rathke's cleft cysts", "cleft cysts, Rathke's", "Central nervous system cyst", "Central Nervous System Cyst", "central nervous system cyst", "Central Nervous System Cysts", "Cysts, Central Nervous System", "cysts, central nervous system", "cyst of central nervous system", "Cyst of central nervous system", "cyst of Central nervous system", "Cyst of Central Nervous System", "Cyst of the central nervous system", "cyst of the Central nervous system", "Cyst of the Central Nervous System", "central nervous system cyst (disease)", "Cyst of central nervous system (disorder)", "cyst of central nervous system (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system cyst", "shortest_name_length": 8}
{"curie": "EFO:0009706", "names": ["latent autoimmune diabetes in adults"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "latent autoimmune diabetes in adults", "shortest_name_length": 36}
{"curie": "UMLS:C5446430", "names": ["Benign Lacrimal Drainage System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Lacrimal Drainage System Neoplasm", "shortest_name_length": 40}
{"curie": "MONDO:0011011", "names": ["GURRIERI syndrome", "GURRIERI SYNDROME", "Gurrieri syndrome", "Gurrieri-Sammito-Bellussi syndrome", "Gurrieri Sammito Bellussi syndrome", "Skeletal dysplasia epilepsy short stature", "Skeletal dysplasia-epilepsy-short stature syndrome", "skeletal dysplasia-epilepsy-short stature syndrome", "skeletal dysplasia with epilepsy and short stature syndrome", "Skeletal dysplasia with epilepsy and short stature syndrome", "mental retardation, epilepsy, short stature and skeletal dysplasia", "mental retardation-epilepsy-short stature-skeletal dysplasia syndrome", "Skeletal dysplasia with epilepsy and short stature syndrome (disorder)", "intellectual disability, epilepsy, short stature and skeletal dysplasia", "skeletal dysplasia with epilepsy and short stature syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skeletal dysplasia-epilepsy-short stature syndrome", "shortest_name_length": 17}
{"curie": "MONDO:0017639", "names": ["CO-induced parkinsonism", "Carbon monoxide-induced parkinsonism", "carbon monoxide-induced parkinsonism", "Delayed encephalopathy due to CO poisoning", "Carbon monoxide-induced parkinsonism (disorder)", "Delayed encephalopathy due to carbon monoxide poisoning"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carbon monoxide-induced parkinsonism", "shortest_name_length": 23}
{"curie": "UMLS:C0016033", "names": ["disease fibrocystic", "fibrocystic disease", "Fibrocystic disease", "diseases fibrocystic", "Fibrocystic disease, NOS", "Nonproliferative fibrocystic disease", "Nonproliferative fibrocystic disease, NOS", "Nonproliferative fibrocystic disease (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nonproliferative fibrocystic disease", "shortest_name_length": 19}
{"curie": "MONDO:0007951", "names": ["masseter muscle Hypertrophy", "Masseter Muscle Hypertrophy", "Masseter muscle hypertrophy", "masseter muscle hypertrophy", "MASSETER MUSCLE HYPERTROPHY", "hypertrophy of masseter muscle", "Masticatory muscle hypertrophy", "Hypertrophy of masseter muscle", "MASTICATORY MUSCLES, HYPERTROPHY OF", "Masticatory Muscles, Hypertrophy of", "masticatory muscles, hypertrophy of", "Hypertrophy of muscles of mastication", "masseter muscle hypertrophy was noted", "Hypertrophy of masseter muscle (disorder)", "Hypertrophy of muscles of mastication (finding)", "hypertrophy of masseter muscle (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "masticatory muscles, hypertrophy of", "shortest_name_length": 27}
{"curie": "MONDO:0013417", "names": ["C3d", "C3D", "C3 DEFICIENCY", "C3 deficiency", "C3 Deficiency", "Complement component 3 deficiency", "complement component 3 deficiency", "C3 deficiency, autosomal recessive", "C3 Deficiency, Autosomal Recessive", "C3 DEFICIENCY, AUTOSOMAL RECESSIVE", "Complement component 3 deficiency (disorder)", "C3 classic complement early component deficiency", "complement component 3 deficiency, autosomal recessive", "Complement Component 3 Deficiency, Autosomal Recessive", "COMPLEMENT COMPONENT 3 DEFICIENCY, AUTOSOMAL RECESSIVE", "classic complement early component deficiency caused by mutation in C3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complement component 3 deficiency", "shortest_name_length": 3}
{"curie": "MONDO:0002963", "names": ["Acantholytic acanthoma", "acantholytic acanthoma", "Acantholytic Acanthoma", "Acantholytic acanthoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acantholytic acanthoma", "shortest_name_length": 22}
{"curie": "UMLS:C0343089", "names": ["Lymphangioma Circumscriptum", "lymphangioma circumscriptum", "Lymphangioma circumscriptum", "Lymphangioma circumscriptum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphangioma circumscriptum", "shortest_name_length": 27}
{"curie": "MONDO:0019587", "names": ["autosomal dominant deafness", "deafness, autosomal dominant", "autosomal dominant isolated deafness", "autosomal dominant nonsyndromic deafness", "nonsyndromic deafness, autosomal dominant", "autosomal dominant nonsyndromic hearing loss", "autosomal dominant nonsyndromic genetic deafness", "nonsyndromic genetic deafness, autosomal dominant", "autosomal dominant nonsyndromic hearing impairment", "autosomal dominant nonsyndromic hearing loss and deafness", "autosomal dominant isolated neurosensory deafness type DFNA", "autosomal dominant isolated sensorineural deafness type DFNA", "autosomal dominant isolated neurosensory hearing loss type DFNA", "autosomal dominant isolated sensorineural hearing loss type DFNA", "autosomal dominant non-syndromic neurosensory deafness type DFNA", "autosomal dominant non-syndromic sensorineural deafness type DFNA", "autosomal dominant non-syndromic neurosensory hearing loss type DFNA", "autosomal dominant non-syndromic sensorineural hearing loss type DFNA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss", "shortest_name_length": 27}
{"curie": "MONDO:0005363", "names": ["inherited focal segmental glomerulosclerosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited focal segmental glomerulosclerosis", "shortest_name_length": 44}
{"curie": "MONDO:0005202", "names": ["ATOPY", "atopy", "Atopy", "Atopic", "atopic", "Atopic state", "atopic state", "allergy atopic", "atopic allergy", "Atopic allergy", "ALLERGY ATOPIC", "Atopic Allergy", "Atopy (finding)", "Atopic reaction", "atopic diathesis", "atopic reactions", "Atopic diathesis", "allergies atopic", "Atopic reaction, NOS", "Atopic reaction (disorder)", "Atopic IgE-mediated allergic disorder", "atopic IgE-mediated allergic disorder", "Atopic immunoglobulin E-mediated allergic disorder", "Atopic immunoglobulin E-mediated allergic disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atopic IgE-mediated allergic disorder", "shortest_name_length": 5}
{"curie": "UMLS:C0235329", "names": ["SMALL BOWEL OBSTRUCTION", "Small bowel obstruction", "bowel obstruction small", "small bowel obstruction", "bowel obstructions small", "SMALL INTESTINE OBSTRUCTION", "Small intestine obstruction", "Obstruction small intestine", "obstruction small intestine", "OBSTRUCTION SMALL INTESTINE", "small intestine obstruction", "small intestinal obstruction", "Small intestinal obstruction", "intestines obstruction small", "Small Intestinal Obstruction", "SBO - Small bowel obstruction", "obstruction of small intestine", "Small intestinal obstruction NOS", "Small bowel obstruction (disorder)", "obstruction of small intestine (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small bowel obstruction", "shortest_name_length": 23}
{"curie": "UMLS:C5670546", "names": ["Posterior Fossa Ependymoma, NEC", "Posterior Fossa Ependymoma, Not Elsewhere Classified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Posterior Fossa Ependymoma, Not Elsewhere Classified", "shortest_name_length": 31}
{"curie": "UMLS:C3828369", "names": ["Rare Malignant Neoplasm", "Rare Malignant Childhood Neoplasm", "Rare Childhood Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rare Childhood Malignant Neoplasm", "shortest_name_length": 23}
{"curie": "OMIM:181300", "names": ["SCAPULA, CONTOUR OF VERTEBRAL BORDER OF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 39}
{"curie": "MONDO:0011423", "names": ["LGMD2E", "LGMDR4", "LGMD type 2E", "Beta-sarcoglycanopathy", "beta-sarcoglycanopathy", "Beta-sarcoglycan-related LGMD R4", "Limb-Girdle Muscular Dystrophy Type 2E", "Limb-girdle muscular dystrophy type 2E", "limb-girdle muscular dystrophy type 2E", "Limb girdle muscular dystrophy type 2E", "Limb-girdle muscular dystrophy, type 2E", "LGMD due to beta-sarcoglycan deficiency", "Muscular Dystrophy, Limb-Girdle, Type 2E", "muscular dystrophy, limb-girdle, type 2E", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2E", "Beta-sarcoglycan limb-girdle muscular dystrophy", "Autosomal Recessive Limb-Girdle Muscular Dystrophy-4", "muscular dystrophy, limb-girdle, autosomal recessive 4", "MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 4", "SGCB autosomal recessive limb-girdle muscular dystrophy", "Beta-Sarcoglycan-Related Limb-Girdle Muscular Dystrophy R4", "Beta-sarcoglycan-related limb-girdle muscular dystrophy R4", "Autosomal recessive limb-girdle muscular dystrophy type 2E", "Autosomal recessive limb girdle muscular dystrophy type 2E", "autosomal recessive limb-girdle muscular dystrophy type 2E", "muscular dystrophy limb-girdle with beta-sarcoglycan deficiency", "Muscular dystrophy limb-girdle with beta-sarcoglycan deficiency", "limb-girdle muscular dystrophy due to beta-sarcoglycan deficiency", "Limb-girdle muscular dystrophy due to beta-sarcoglycan deficiency", "Limb girdle muscular dystrophy due to beta-sarcoglycan deficiency", "Autosomal recessive limb girdle muscular dystrophy type 2E (disorder)", "autosomal recessive limb-girdle muscular dystrophy caused by mutation in SGCB"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive limb-girdle muscular dystrophy type 2E", "shortest_name_length": 6}
{"curie": "MONDO:0100230", "names": ["FAR1 dysregulation", "fatty acyl-CoA reductase 1 dysregulation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fatty acyl-CoA reductase 1 dysregulation", "shortest_name_length": 18}
{"curie": "UMLS:C4552925", "names": ["Stage IB Uterine Corpus Cancer AJCC v8", "Stage IB Uterine (including Endometrial) Cancer", "Stage IB Uterine Corpus Carcinoma or Carcinosarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Uterine Corpus Cancer AJCC v8", "shortest_name_length": 38}
{"curie": "MONDO:0013792", "names": ["ich", "ICH", "Brain bleeding", "Hematencephalon", "CVA; hemorrhagic", "hemorrhagic; CVA", "brain hemorrhage", "Brain Hemorrhage", "Hemorrhage brain", "HEMORRHAGE BRAIN", "Brain hemorrhage", "Haematencephalon", "BRAIN, HEMORRHAGE", "brain hemorrhages", "brain haemorrhage", "Brain Hemorrhages", "Cerebral bleeding", "brain; hemorrhage", "Haemorrhage brain", "Brain--Hemorrhage", "hemorrhage; brain", "Hemorrhage, Brain", "Bleeding in brain", "hemorrhagic stroke", "Hemorrhagic Stroke", "stroke hemorrhagic", "Hemorrhagic stroke", "HEMORRHAGIC STROKE", "Hemorrhages, Brain", "Stroke, Hemorrhagic", "stroke, hemorrhagic", "Intracerebral bleed", "Haemorrhagic stroke", "Cerebrum Hemorrhage", "Hemorrhage cerebral", "hemorrhagic strokes", "Hemorrhagic Strokes", "cerebral hemorrhage", "Stroke, hemorrhagic", "CEREBRAL HEMORRHAGE", "HEMORRHAGE CEREBRAL", "Cerebral hemorrhage", "intracerebral bleed", "haemorrhagic stroke", "Cerebral Hemorrhage", "CEREBRAL HAEMORRHAGE", "Haemorrhage cerebral", "Hemorrhage, Cerebral", "Hemorrhagic cerebrum", "cerebral hemorrhages", "Hemorrhage, Cerebrum", "Cerebral haemorrhage", "Cerebral hemorrhages", "Cerebral Hemorrhages", "cerebral haemorrhage", "Cerebrum Hemorrhages", "Hemorrhage, cerebral", "Haemorrhage;cerebral", "cerebral haemorrhages", "Hemorrhages, Cerebral", "Hemorrhages, Cerebrum", "Haemorrhagic cerebrum", "intracerebral hematoma", "Hemorrhage of cerebrum", "HEMORRHAGE INTRACEREBRAL", "intracerebral hemorrhage", "Intracerebral Hemorrhage", "Intracerebral hemorrhage", "Hemorrhage intracerebral", "INTRACEREBRAL HEMORRHAGE", "Parenchymatous Hemorrhage", "Intracerebral haemorrhage", "intracerebral haemorrhage", "intracerebral hemorrhages", "Intra-cerebral hemorrhage", "Haemorrhage intracerebral", "Cerebral Brain Hemorrhage", "Hemorrhage, Intracerebral", "Intracerebral Hemorrhages", "hemorrhage; intracerebral", "intracerebral; hemorrhage", "Rupture;blood vessel;brain", "Hemorrhages, Intracerebral", "Brain Hemorrhage, Cerebral", "Cerebral Brain Hemorrhages", "Intra-cerebral haemorrhage", "Hemorrhage, Cerebral Brain", "Hemorrhages, Cerebral Brain", "Brain Hemorrhages, Cerebral", "Intracerebral hemorrhage, NOS", "Cerebral hemorrhage (disorder)", "Intracerebral haemorrhage, NOS", "ICH - Intracerebral hemorrhage", "hemorrhagic stroke (diagnosis)", "ICH - intracerebral hemorrhage", "Cerebral parenchymal hemorrhage", "hemorrhagic cerebral infarction", "ICH - Intracerebral haemorrhage", "ICH - intracerebral haemorrhage", "Hemorrhagic cerebral infarction", "Cerebral Parenchymal Hemorrhage", "cerebral infarction hemorrhagic", "CEREBRAL PARENCHYMAL HEMORRHAGE", "haemorrhagic cerebral infarction", "Rupture of blood vessel in brain", "Cerebral parenchymal haemorrhage", "Hemorrhage, Cerebral Parenchymal", "Parenchymal Hemorrhage, Cerebral", "Cerebral Parenchymal Hemorrhages", "Haemorrhagic cerebral infarction", "Hemorrhages, Cerebral Parenchymal", "Parenchymal Hemorrhages, Cerebral", "intracerebral hemorrhage (diagnosis)", "Hemorrhagic Cerebrovascular Accident", "rupture of blood vessels in the brain", "Intracerebral hemorrhage, unspecified", "Stroke due to intracerebral hemorrhage", "STROKE, HEMORRHAGIC, SUSCEPTIBILITY TO", "Intracerebral haemorrhage, unspecified", "cerebrovascular; accident, hemorrhagic", "accident; cerebrovascular, hemorrhagic", "stroke, hemorrhagic, susceptibility to", "Stroke due to intracerebral haemorrhage", "Hemorrhagic cerebral infarction (disorder)", "Hemorrhagic cerebral infarction (diagnosis)", "hemorrhage, intracerebral, susceptibility to", "HEMORRHAGE, INTRACEREBRAL, SUSCEPTIBILITY TO", "CVA - Cerebrovascular accident due to intracerebral hemorrhage", "CVA - Cerebrovascular accident due to intracerebral haemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intracerebral hemorrhage", "shortest_name_length": 3}
{"curie": "MONDO:0012526", "names": ["HAE3", "HAE 3", "Hae 3", "HAE-III", "Estrogen Related HAE", "Estrogen-Related HAE", "ESTROGEN-RELATED HAE", "estrogen-related Hae", "Estrogen-Related HAEs", "HAE, Estrogen-Related", "HAE with normal C1Inh", "Estrogen Sensitive HAE", "HAEs, Estrogen-Related", "estrogen-sensitive Hae", "Estrogen-Sensitive HAE", "ESTROGEN-SENSITIVE HAE", "HAE, Estrogen-Sensitive", "Estrogen-Sensitive HAEs", "HAEs, Estrogen-Sensitive", "ANGIOEDEMA, HEREDITARY, 3", "F12 hereditary angioedema", "angioedema, hereditary, 3", "HAE with normal C1 inhibitor", "Hereditary angioedema type 3", "hereditary angioedema type 3", "Hereditary Angioedema Type III", "Hereditary angioedema type III", "Hereditary angioedema - type 3", "angioedema, hereditary, type 3", "hereditary angioedema type III", "ANGIOEDEMA, HEREDITARY, TYPE III", "angioedema, hereditary, type III", "Angioedema, Hereditary, Type III", "hereditary angioneurotic edema type 3", "Hereditary angioneurotic edema type 3", "inherited estrogen-dependent angioedema", "Hereditary angioedema with normal C1Inh", "Inherited estrogen-dependent angioedema", "Inherited estrogen-associated angioedema", "Estrogen-Sensitive Hereditary Angioedema", "Estrogen Sensitive Hereditary Angioedema", "inherited estrogen-associated angioedema", "F12-related HAE with normal C1 inhibitor", "Hereditary Angioedema, Estrogen-Sensitive", "Angioedema, Estrogen-Sensitive Hereditary", "Estrogen-Sensitive Hereditary Angioedemas", "Hereditary Angioedemas, Estrogen-Sensitive", "Angioedemas, Estrogen-Sensitive Hereditary", "Hereditary angioedema with normal C1 inhibitor", "hereditary angioedema caused by mutation in F12", "inherited estrogen-dependent angioneurotic edema", "Hereditary angioneurotic edema with normal C1Inh", "Inherited estrogen-dependent angioneurotic edema", "inherited estrogen-associated angioneurotic edema", "Inherited estrogen-associated angioneurotic edema", "F12-related hereditary angioedema with normal C1Inh", "Hereditary Angioedema with Normal C1 Inhibitor Activity", "Hereditary angioneurotic edema with normal C1 inhibitor", "HAE WITH NORMAL C1 INHIBITOR CONCENTRATION AND FUNCTION", "HEREDITARY ANGIOEDEMA WITH NORMAL C1 INHIBITOR ACTIVITY", "hereditary angioedema with normal C1 inhibitor activity", "Hae with normal C1 inhibitor concentration and function", "HAE with Normal C1 Inhibitor Concentration and Function", "Hereditary angioedema with normal C1 esterase inhibitor activity", "Hereditary angio-oedema with normal C1 esterase inhibitor activity", "Hereditary angioneurotic edema with normal C1 esterase inhibitor activity", "Hereditary angioneurotic oedema with normal C1 esterase inhibitor activity", "Hereditary angioedema with normal C1 esterase inhibitor activity (disorder)", "Hereditary angioedema with normal C1 esterase inhibitor activity (diagnosis)", "Angioneurotic Edema, Hereditary, with Normal C1 Inhibitor Concentration and Function", "ANGIONEUROTIC EDEMA, HEREDITARY, WITH NORMAL C1 INHIBITOR CONCENTRATION AND FUNCTION", "angioneurotic edema, hereditary, with normal C1 inhibitor concentration and function"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary angioedema type 3", "shortest_name_length": 4}
{"curie": "UMLS:C4553674", "names": ["Stage IIIA Primary Peritoneal Cancer", "Stage IIIA Primary Peritoneal Cancer AJCC v8", "Stage IIIA Primary Peritoneal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Primary Peritoneal Cancer AJCC v8", "shortest_name_length": 36}
{"curie": "MONDO:0012804", "names": ["CMH12", "hypertrophic cardiomyopathy 12", "cardiomyopathy, hypertrophic, 12", "CSRP3 hypertrophic cardiomyopathy", "hypertrophic cardiomyopathy type 12", "cardiomyopathy familial hypertrophic 12", "cardiomyopathy, familial hypertrophic, 12", "CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12", "cardiomyopathy, familial hypertrophic, type 12", "hypertrophic cardiomyopathy caused by mutation in CSRP3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophic cardiomyopathy 12", "shortest_name_length": 5}
{"curie": "UMLS:C4744855", "names": ["Benign Genitourinary System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Genitourinary System Neoplasm", "shortest_name_length": 36}
{"curie": "MONDO:0016545", "names": ["leukoencephalopathy palmoplantar keratoderma", "leukoencephalopathy-palmoplantar keratoderma syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukoencephalopathy-palmoplantar keratoderma syndrome", "shortest_name_length": 44}
{"curie": "UMLS:C4682634", "names": ["Stage IVB Fallopian Tube Cancer", "Stage IVB Fallopian Tube Cancer AJCC v8", "Stage IVB Fallopian Tube Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Fallopian Tube Cancer AJCC v8", "shortest_name_length": 31}
{"curie": "MONDO:0016154", "names": ["qualitative or quantitative defects of myotubularin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of myotubularin", "shortest_name_length": 51}
{"curie": "MONDO:0010017", "names": ["Sea-blue histiocyte", "Sea-blue histiocytosis", "SEA-BLUE HISTIOCYTOSIS", "sea-blue histiocytosis", "Sea-Blue Histiocytoses", "Sea-Blue Histiocytosis", "Sea Blue Histiocytoses", "sea blue histiocytosis", "Sea Blue Histiocytosis", "Histiocytoses, Sea-Blue", "Histiocytosis, Sea-Blue", "Histiocytosis, Sea Blue", "HISTIOCYTOSIS, SEA-BLUE", "Histiocytoses, Sea Blue", "histiocytosis, Sea-blue", "SEA-BLUE HISTIOCYTE DISEASE", "Sea Blue Histiocyte Disease", "SEA-blue histiocyte disease", "Sea-Blue Histiocyte Disease", "Sea-Blue Histiocyte Diseases", "Sea Blue Histiocyte Syndrome", "Histiocyte Disease, Sea-Blue", "Sea-blue histiocyte syndrome", "Sea-Blue Histiocyte Syndrome", "sea-blue histiocyte syndrome", "Disease, Sea-Blue Histiocyte", "Sea-Blue Histiocyte Syndromes", "Histiocyte Syndrome, Sea Blue", "Syndrome, Sea-Blue Histiocyte", "Histiocyte Syndrome, Sea-Blue", "Histiocyte Diseases, Sea-Blue", "Diseases, Sea-Blue Histiocyte", "Histiocyte Syndromes, Sea Blue", "Syndromes, Sea-Blue Histiocyte", "Histiocyte Syndromes, Sea-Blue", "inherited Lipemic splenomegaly", "Sea-blue histiocyte syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sea-blue histiocyte syndrome", "shortest_name_length": 19}
{"curie": "MONDO:0009763", "names": ["Pickwickian Syndrome", "pickwickian syndrome", "Pickwickian syndrome", "PICKWICKIAN SYNDROME", "obesity hypoventilation syndrome", "Obesity-Hypoventilation Syndrome", "Pickwickian syndrome (diagnosis)", "OBESITY-HYPOVENTILATION SYNDROME", "Obesity hypoventilation syndrome", "Obesity Hypoventilation Syndrome", "obesity-hypoventilation syndrome", "CARDIOPULMONARY OBESITY SYNDROME", "OBESITY HYPOVENTILATION SYNDROME", "hypoventilation obesity syndrome", "syndrome; cardiopulmonary-obesity", "Hypoventilation Syndrome, Obesity", "cardiopulmonary; obesity syndrome", "Obesity-Hypoventilation Syndromes", "HYPOVENTILATION ASSOCIATED WITH OBESITY", "Extreme obesity with alveolar hypoventilation", "Hypoventilation associated with obesity syndrome", "Extreme obesity with alveolar hypoventilation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "obesity-hypoventilation syndrome", "shortest_name_length": 20}
{"curie": "UMLS:C5206566", "names": ["Refractory High-Grade B-Cell Lymphoma with MYC, BCL2, and BCL6 Rearrangements", "Refractory High Grade B-Cell Lymphoma with MYC, BCL2, and BCL6 Rearrangements"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory High Grade B-Cell Lymphoma with MYC, BCL2, and BCL6 Rearrangements", "shortest_name_length": 77}
{"curie": "UMLS:C0751893", "names": ["Posterior Fossa Hemorrhage", "posterior fossa; hemorrhage", "fossa posterior; hemorrhage", "Posterior Fossa Hemorrhages", "Hemorrhage, Posterior Fossa", "hemorrhage; posterior fossa", "Hemorrhages, Posterior Fossa"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Posterior Fossa Hemorrhage", "shortest_name_length": 26}
{"curie": "MONDO:0013703", "names": ["MRT33", "mental retardation, autosomal recessive 33", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 33", "intellectual disability, autosomal recessive 33", "autosomal recessive intellectual developmental disorder 33", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 33"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 33", "shortest_name_length": 5}
{"curie": "MONDO:0007515", "names": ["Corectopia", "corectopia", "ectopic pupil", "Ectopic Pupil", "Ectopic pupil", "ectopia; pupil", "Pupil, Ectopic", "Ectopic Pupils", "pupil; ectopia", "ectopic pupils", "Displaced pupil", "Pupils, Ectopic", "ectopia pupillae", "Ectopia pupillae", "Displaced pupils", "ECTOPIA PUPILLAE", "Familial ectopic pupil", "corectopia (diagnosis)", "familial ectopic pupil", "congenital ectopic pupil", "Ectopic pupil (disorder)", "Congenital ectopic pupil", "ectopic pupil (diagnosis)", "ectopia pupillae (disease)", "ectopic pupil (physical finding)", "Congenital ectopic pupil (disorder)", "congenital ectopic pupil (diagnosis)", "congenital eye malformation in which the pupils are displaced from their normal central position"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectopia pupillae", "shortest_name_length": 10}
{"curie": "UMLS:C4521727", "names": ["Stage IV Esophageal Squamous Cell Cancer", "Clinical Stage IV Esophageal Squamous Cell Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage IV Esophageal Squamous Cell Carcinoma AJCC v8", "shortest_name_length": 40}
{"curie": "MONDO:0001764", "names": ["ethmoid sinus tumor", "Ethmoid Sinus Tumor", "ethmoidal sinus tumor", "Ethmoidal Sinus Tumor", "ethmoid sinus neoplasm", "tumor of ethmoid sinus", "Tumor of ethmoid sinus", "Tumor of Ethmoid Sinus", "Ethmoid Sinus Neoplasm", "Tumour of ethmoid sinus", "Tumor of Ethmoidal Sinus", "tumor of ethmoidal sinus", "Ethmoidal Sinus Neoplasm", "ethmoidal sinus neoplasm", "Neoplasm of Ethmoid Sinus", "neoplasm of ethmoid sinus", "tumor of the ethmoid sinus", "Tumor of the Ethmoid Sinus", "Neoplasm of ethmoidal sinus", "neoplasm of ethmoidal sinus", "Neoplasm of Ethmoidal Sinus", "Tumor of the Ethmoidal Sinus", "tumor of the ethmoidal sinus", "Neoplasm of the Ethmoid Sinus", "neoplasm of the ethmoid sinus", "ethmoidal sinus benign neoplasm", "Neoplasm of the Ethmoidal Sinus", "neoplasm of the ethmoidal sinus", "ethmoid sinus neoplasm (disease)", "neoplasm of ethmoid sinus (diagnosis)", "Neoplasm of ethmoidal sinus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ethmoidal sinus neoplasm", "shortest_name_length": 19}
{"curie": "UMLS:C0279742", "names": ["Grade II Salivary Gland Mucoepidermoid Carcinoma", "Grade II Mucoepidermoid Carcinoma of Salivary Gland", "Grade II Mucoepidermoid Carcinoma of the Salivary Gland", "Intermediate Grade Salivary Gland Mucoepidermoid Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intermediate Grade Salivary Gland Mucoepidermoid Carcinoma", "shortest_name_length": 48}
{"curie": "UMLS:C1509149", "names": ["Subepidermal Nodular Fibrosis", "Subepidermal nodular fibrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Subepidermal Nodular Fibrosis", "shortest_name_length": 29}
{"curie": "UMLS:C2983701", "names": ["Esophageal Cancer by AJCC v6 Stage", "Esophageal Carcinoma by AJCC v6 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Cancer by AJCC v6 Stage", "shortest_name_length": 34}
{"curie": "MONDO:0005119", "names": ["Charbon", "ANTHRAX", "charbon", "anthrax", "Anthrax", "CHARBON", "Milzbrand", "MILZBRAND", "Anthrax, NOS", "splenic fever", "Splenic fever", "SPLENIC FEVER", "FEVER, SPLENIC", "Anthrax disease", "anthrax disease", "anthrax infection", "Anthrax (disorder)", "anthrax; infection", "anthrax (diagnosis)", "Anthrax, unspecified", "Bacillus anthracis infection", "Bacillus anthracis Infection", "Bacillus anthracis Infections", "infection due to Bacillus anthracis", "Infection due to Bacillus anthracis", "Bacillus anthracis infectious disease", "Bacillus anthracis disease or disorder", "Bacillus anthracis caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anthrax infection", "shortest_name_length": 7}
{"curie": "MONDO:0700051", "names": ["liver abscess", "LIVER ABSCESS", "Abscess;liver", "Liver Abscess", "abscess liver", "Liver abscess", "abscess; liver", "liver; abscess", "Abscess, Liver", "Liver--Abscess", "abscessed liver", "abscess hepatic", "Hepatic abscess", "hepatic abscess", "Hepatic Abscess", "Liver Abscesses", "liver abscesses", "abscess of liver", "Abscess of liver", "Abscess, Hepatic", "Abscesses, Liver", "of liver abscess", "Hepatic Abscesses", "abscesses hepatic", "Abscesses, Hepatic", "Hepatic abscess NOS", "Hepatic abscess, NOS", "Abscess of liver, NOS", "liver abscess (disease)", "liver abscess (diagnosis)", "Abscess of liver (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "liver abscess (disease)", "shortest_name_length": 13}
{"curie": "MONDO:0006710", "names": ["psychomotor epilepsy", "PSYCHOMOTOR EPILEPSY", "Psychomotor epilepsy", "epilepsy psychomotor", "Psychomotor Epilepsy", "Epilepsy, Psychomotor", "Epilepsy, psychomotor", "epilepsy; psychomotor", "EPILEPSY, PSYCHOMOTOR", "epilepsy, psychomotor", "PARTIAL COMPLEX EPILEPSY", "complex partial epilepsy", "Complex Partial Epilepsy", "Complex partial epilepsy", "partial complex epilepsy", "Partial Epilepsy, Complex", "Epilepsy, Complex Partial", "Psychic Equivalent Epilepsy", "Epilepsy, Psychic Equivalent", "Psychomotor epilepsy (disorder)", "Complex Partial Seizure Disorder", "Psychomotor epilepsy (diagnosis)", "partial complex seizure disorder", "complex partial seizure disorder", "Seizure Disorder, Complex Partial", "Complex partial epileptic seizure", "Disorder, Complex Partial Seizures", "epilepsy; complex partial seizures", "partial complex psychomotor seizure", "complex partial seizures; epileptic", "seizure; epileptic, complex, partial", "epilepsy localization-related psychomotor", "Complex partial epileptic seizure (disorder)", "epilepsy; syndrome, complex partial seizures", "partial complex psychomotor seizure (diagnosis)", "epilepsy; syndrome, with complex partial seizures", "syndrome; epileptic, with complex partial seizures"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "complex partial epilepsy", "shortest_name_length": 20}
{"curie": "MONDO:0019852", "names": ["inherited primary ovarian failure", "hereditary primary ovarian failure", "inherited premature ovarian failure", "non-acquired premature ovarian failure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited primary ovarian failure", "shortest_name_length": 33}
{"curie": "UMLS:C4086173", "names": ["Childhood Testicular Immature Teratoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Testicular Immature Teratoma", "shortest_name_length": 38}
{"curie": "UMLS:C1608965", "names": ["Drug exposure before pregnancy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drug exposure before pregnancy", "shortest_name_length": 30}
{"curie": "UMLS:C4049636", "names": ["R1", "ROSE Cluster 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ROSE Cluster 1", "shortest_name_length": 2}
{"curie": "UMLS:C4744729", "names": ["Advanced Cervical Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Cervical Adenocarcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0000636", "names": ["musculoskeletal system benign neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "musculoskeletal system benign neoplasm", "shortest_name_length": 38}
{"curie": "MONDO:0016201", "names": ["qualitative or quantitative defects of myotilin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of myotilin", "shortest_name_length": 47}
{"curie": "UMLS:C3897234", "names": ["Untreated Fibrillary Astrocytoma", "Untreated Childhood Fibrillary Astrocytoma", "untreated childhood fibrillary astrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Untreated Childhood Fibrillary Astrocytoma", "shortest_name_length": 32}
{"curie": "UMLS:C4744488", "names": ["Recurrent Neurofibromatosis Type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Neurofibromatosis Type 1", "shortest_name_length": 34}
{"curie": "UMLS:C0332686", "names": ["Burn erythema", "Epidermal burn", "superficial burn", "Erythema Ab Igne", "Superficial burn", "Erythema ab igne", "burns superficial", "First degree burn", "eczema; hot place", "first degree burn", "erythema; ab igne", "First-Degree Burn", "ab igne; erythema", "burn degree first", "First Degree Burn", "First degree burns", "Erythema caloricum", "first degree burns", "burns degree first", "Burns first degree", "Burn erythema of skin", "Epidermal burn of skin", "SKIN BURN DEGREE FIRST", "Burn(s);skin;1st degree", "First degree burn injury", "Superficial burn of skin", "First degree burn of skin", "Erythema ab igne - disorder", "1st degree burn of the skin", "Erythema ab igne (disorder)", "first degree burns (diagnosis)", "Superficial (First Degree) Burn", "superficial (first degree) burns", "Erythema, body region unspecified", "Epidermal burn of skin (disorder)", "erythema ab igne [dermatitis ab igne]", "Erythema ab igne [dermatitis ab igne]", "Erythema due to burn, unspecified site", "Erythema [first degree], unspecified site", "Burn of first degree, body region unspecified", "erythema ab igne [dermatitis ab igne] (diagnosis)", "First degree burn injury (morphologic abnormality)", "Erythema due to first degree burn, unspecified site", "Erythema due to burn (first degree), unspecified site", "Erythema due to burn [first degree], unspecified site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epidermal burn of skin", "shortest_name_length": 13}
{"curie": "UMLS:C2828184", "names": ["Stage IB Gestational Trophoblastic Tumor", "Stage IB Gestational Trophoblastic Tumor AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IB Gestational Trophoblastic Tumor AJCC v7", "shortest_name_length": 40}
{"curie": "UMLS:C0852874", "names": ["Moraxella infection", "Moraxella Infection", "Moraxella Infections", "Moraxella infections", "Infection, Moraxella", "Infections, Moraxella", "Moraxella infection NOS", "disease due to Moraxella", "Disease due to Moraxella", "Disease caused by Moraxella", "disease due to Moraxella (diagnosis)", "Disease caused by Moraxella (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Moraxella Infections", "shortest_name_length": 19}
{"curie": "MONDO:0010014", "names": ["CRMDD", "Schwartz-Lelek syndrome", "CRANIOMETADIAPHYSEAL dysplasia", "craniometadiaphyseal dysplasia, wormian bone type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "craniometadiaphyseal dysplasia, wormian bone type", "shortest_name_length": 5}
{"curie": "MONDO:0007963", "names": ["CMM1", "B-K Mole syndrome", "melanoma, familial", "melanoma, malignant", "melanoma, malignant, somatic", "melanoma, cutaneous malignant", "melanoma, cutaneous malignant, 1", "MELANOMA, CUTANEOUS MALIGNANT, 1", "dysplastic Nevus syndrome, hereditary", "familial atypical Mole-malignant melanoma syndrome", "MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 1", "melanoma, cutaneous malignant, susceptibility to, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melanoma, cutaneous malignant, susceptibility to, 1", "shortest_name_length": 4}
{"curie": "MONDO:0022854", "names": ["congenital unilateral pulmonary hypoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital unilateral pulmonary hypoplasia", "shortest_name_length": 42}
{"curie": "MONDO:0008082", "names": ["MEN 3", "MEN2B", "MEN2b", "men 2b", "MEN 2b", "MEA 2b", "MEN 2B", "men 2B", "MEA IIb", "MEN III", "MEN IIB", "men iii", "men iib", "men IIB", "MEN IIb", "MEN, type 3", "MEN Type 2B", "men type 2B", "men type IIB", "MEN type IIB", "MEN Type IIB", "MEN 3 syndrome", "MEN3, FORMERLY", "MEN 2B syndrome", "MEA syndrome, type IIb", "Mucosal neuroma syndrome", "mucosal neuroma syndrome", "Mucosal Neuroma Syndrome", "mucosal Neuroma syndrome", "MUCOSAL NEUROMA SYNDROME", "Mucosal Neuroma Syndromes", "Neuroma Syndrome, Mucosal", "Wagenmann-Froboese Syndrome", "WAGENMANN-FROBOESE SYNDROME", "Wagenmann-Froboese syndrome", "Wagenmann Froboese Syndrome", "Syndrome, Wagenmann-Froboese", "multiple endocrine neoplasia IIB", "multiple endocrine neoplasia type 3", "Multiple endocrine neoplasia type 3", "Multiple Endocrine Neoplasia Type 3", "Multiple Endocrine Neoplasms Type 2b", "multiple endocrine neoplasia, type 3", "Multiple endocrine neoplasia, type 3", "multiple endocrine neoplasia type 2B", "Multiple endocrine neoplasia type 2B", "Multiple Endocrine Neoplasia Type 2B", "Multiple endocrine neoplasia Type 2B", "Multiple Endocrine Neoplasia Type 2b", "Neoplasms, Multiple Endocrine Type 2b", "Multiple Endocrine Neoplasia, Type 2b", "Multiple Endocrine Neoplasia Type III", "Neoplasia, Multiple Endocrine Type 2b", "Multiple endocrine neoplasia, type 2b", "multiple endocrine neoplasia type IIB", "multiple endocrine neoplasia, type 2B", "Multiple Endocrine Neoplasia Type IIB", "Multiple endocrine neoplasia type III", "type IIb multiple endocrine neoplasia", "Multiple endocrine neoplasia Type IIB", "multiple endocrine neoplasia type III", "multiple endocrine neoplasia, type III", "MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB", "multiple endocrine neoplasia, type IIB", "Multiple Endocrine Neoplasia, Type IIb", "Multiple Endocrine Neoplasia, Type III", "multiple endocrine adenomatosis type IIB", "Multiple Endocrine Adenomatosis Type IIB", "Multiple endocrine adenomatosis Type IIb", "Neuromata, Mucosal, With Endocrine Tumors", "NEUROMATA, MUCOSAL, WITH ENDOCRINE TUMORS", "Multiple endocrine adenomatosis, type IIb", "Neuromata, mucosal, with endocrine tumors", "MEN 3 - Multiple endocrine neoplasia type 3", "Multiple endocrine neoplasia [MEN] type IIB", "MEN2B - multiple endocrine neoplasia type 2B", "MEN 2B - Multiple endocrine neoplasia type 2B", "multiple endocrine neoplasia, type 3 (formerly)", "Multiple endocrine neoplasia, type 3 (disorder)", "multiple endocrine neoplasia, type III, formerly", "MULTIPLE ENDOCRINE NEOPLASIA, TYPE III, FORMERLY", "type IIb multiple endocrine neoplasia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple endocrine neoplasia type 2B", "shortest_name_length": 5}
{"curie": "UMLS:C2930835", "names": ["Optic Disc Edema"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Optic Disc Edema", "shortest_name_length": 16}
{"curie": "MONDO:0003570", "names": ["Lipid-rich carcinoma", "lipid-rich carcinoma", "Lipid-Rich Carcinoma", "carcinoma; lipid-rich", "lipid-rich; carcinoma", "[M] Lipid-rich carcinoma", "lipid-rich carcinoma (morphologic abnormality)", "Lipid-rich carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lipid-rich carcinoma", "shortest_name_length": 20}
{"curie": "MONDO:0100275", "names": ["FAR1 defect", "fatty acyl-CoA reductase defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fatty acyl-CoA reductase defects", "shortest_name_length": 11}
{"curie": "UMLS:C0278734", "names": ["Relapsed Vulva Cancer", "Relapsed Vulvar Cancer", "recurrent vulva cancer", "Recurrent Vulva Cancer", "vulva cancer, recurrent", "recurrent vulvar cancer", "Recurrent Vulvar Cancer", "Relapsed Cancer of Vulva", "vulvar cancer, recurrent", "Recurrent Cancer of Vulva", "Recurrent Vulvar Carcinoma", "Relapsed Cancer of the Vulva", "recurrent cancer of the vulva", "Recurrent Cancer of the Vulva", "cancer of the vulva, recurrent", "recurrent carcinoma of the vulva", "carcinoma of the vulva, recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Vulvar Carcinoma", "shortest_name_length": 21}
{"curie": "UMLS:C0151500", "names": ["Atropine-like syndrome", "ATROPINE-LIKE SYNDROME", "Syndrome atropine-like", "SYNDROME ATROPINE-LIKE", "ANTICHOLINERGIC SYNDROME", "Anticholinergic Syndrome", "Anticholinergic syndrome", "SYNDROME ANTICHOLINERGIC", "Syndrome anticholinergic", "Anticholinergic Syndromes", "Syndrome, Anticholinergic", "Syndrome parasympatholytic", "SYNDROME PARASYMPATHOLYTIC", "Syndromes, Anticholinergic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anticholinergic Syndrome", "shortest_name_length": 22}
{"curie": "MONDO:0043106", "names": ["ichthyosis linearis circumflexa", "Ichthyosis linearis circumflexa", "Ichthyosis linearis circumflexa (disorder)", "ichthyosis congenital linearis circumflexa", "Ichthyosis linearis circumflexa (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ichthyosis linearis circumflexa", "shortest_name_length": 31}
{"curie": "MONDO:0060714", "names": ["HFTC2", "TUMORAL CALCINOSIS, FAMILIAL, HYPERPHOSPHATEMIC, 2", "TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 2", "tumoral calcinosis, hyperphosphatemic, familial, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tumoral calcinosis, hyperphosphatemic, familial, 2", "shortest_name_length": 5}
{"curie": "MONDO:0014985", "names": ["FANCV", "MAD2L2 Fanconi anemia", "Fanconi anemia complementation group V", "Fanconi anemia, complementation GROUP V", "Fanconi Anemia, complementation Group 5", "Fanconi Anemia, complementation group V", "FANCONI ANEMIA, COMPLEMENTATION GROUP V", "Fanconi anemia caused by mutation in MAD2L2", "Fanconi anemia complementation group type V", "Fanconi Anemia, complementation group type V"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fanconi anemia complementation group V", "shortest_name_length": 5}
{"curie": "MONDO:0100232", "names": ["PSORAS1", "psoriatic arthritis, susceptibility", "psoriatic arthritis, susceptibility to", "PSORIATIC ARTHRITIS, SUSCEPTIBILITY TO", "PSORIATIC ARTHRITIS, SUSCEPTIBILITY TO, 1", "PSORIATIC ARTHRITIS, SUSCEPTIBILITY TO (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "psoriatic arthritis, susceptibility to", "shortest_name_length": 7}
{"curie": "UMLS:C1332039", "names": ["AIDS-Related Carcinoma", "AIDS Related Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Carcinoma", "shortest_name_length": 22}
{"curie": "UMLS:C1333551", "names": ["FIGO Stage IC GTT", "FIGO Stage IC Gestational Trophoblastic Tumor", "FIGO Stage IC Gestational Trophoblastic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Stage IC Gestational Trophoblastic Tumor", "shortest_name_length": 17}
{"curie": "MONDO:0003218", "names": ["AIS", "adenocarcinoma situ", "Adenocarcinoma in situ", "in situ adenocarcinoma", "Adenocarcinoma in-situ", "Adenocarcinoma in Situ", "Adenocarcinoma In Situ", "adenocarcinoma in situ", "adenocarcinoma in-situ", "Situ, Adenocarcinoma in", "Adenocarcinoma in Situs", "in Situ, Adenocarcinoma", "Adenocarcinoma in situ NOS", "Preinvasive Adenocarcinoma", "Preinvasive Adenocarcinomas", "Adenocarcinoma, Preinvasive", "Adenocarcinoma in situ, NOS", "Adenocarcinomas, Preinvasive", "AIS - Adenocarcinoma in situ", "Intraepithelial Adenocarcinoma", "Intraepithelial Adenocarcinomas", "Adenocarcinoma, Intraepithelial", "Adenocarcinomas, Intraepithelial", "adenocarcinoma in situ (diagnosis)", "Adenocarcinoma in situ (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenocarcinoma in situ", "shortest_name_length": 3}
{"curie": "MONDO:0012111", "names": ["CMH8", "hypertrophic cardiomyopathy 8", "cardiomyopathy, hypertrophic, 8", "MYL3 hypertrophic cardiomyopathy", "hypertrophic cardiomyopathy type 8", "cardiomyopathy, familial hypertrophic, 8", "CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8", "Cardiomyopathy, Familial Hypertrophic, 8", "cardiomyopathy, familial hypertrophic, type 8", "hypertrophic cardiomyopathy caused by mutation in MYL3", "cardiomyopathy hypertrophic mid-left ventricular chamber type 1", "Cardiomyopathy, Hypertrophic, Mid-Left Ventricular Chamber Type, 1", "CARDIOMYOPATHY, HYPERTROPHIC, MID-LEFT VENTRICULAR CHAMBER TYPE, 1", "cardiomyopathy, hypertrophic, mid-left ventricular chamber type, 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypertrophic cardiomyopathy 8", "shortest_name_length": 4}
{"curie": "UMLS:C0239293", "names": ["esophageal bleed", "bleeding esophageal", "esophageal bleeding", "Esophageal bleeding", "ESOPHAGEAL BLEEDING", "Oesophageal bleeding", "Esophageal hemorrhage", "HEMORRHAGE ESOPHAGEAL", "Hemorrhage esophageal", "hemorrhage; esophagus", "ESOPHAGEAL HEMORRHAGE", "esophageal hemorrhage", "Esophageal Hemorrhage", "esophagus; hemorrhage", "Oesophageal haemorrhage", "Hemorrhage of esophagus", "Haemorrhage oesophageal", "OESOPHAGEAL HAEMORRHAGE", "Haemorrhage of oesophagus", "Hemorrhage of esophagus NOS", "Esophageal bleeding (disorder)", "esophageal hemorrhage (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal bleeding", "shortest_name_length": 16}
{"curie": "MONDO:0021113", "names": ["RESPIRATORY FAILURE", "FAILURE RESPIRATORY", "Respiratory failure", "respiratory failure", "Failure;respiratory", "Respiratory Failure", "RESPIRATION FAILURE", "Respiration failure", "Failure respiratory", "failure, respiratory", "Respiratory Failures", "Failure, Respiratory", "Respiratory failure NOS", "Respiratory failure, NOS", "respiratory insufficiency", "acute respiratory failure", "acute respiratory Failure", "Respiratory Insufficiency", "respiratory failure chronic", "Chronic respiratory failure", "chronic respiratory failure", "Respiratory failure, chronic", "Respiratory failure (disorder)", "respiratory failure (diagnosis)", "Respiratory failure, unspecified", "respiratory insufficiency/failure", "acute-on-chronic respiratory failure", "acute and chronic respiratory failure", "Chronic respiratory failure (disorder)", "chronic respiratory failure (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "respiratory failure", "shortest_name_length": 19}
{"curie": "MONDO:0000155", "names": ["triglyceride storage disease", "inborn error of sequestering of triglyceride", "inborn sequestering of triglyceride disorder", "rare inborn error of sequestering of triglyceride"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "triglyceride storage disease", "shortest_name_length": 28}
{"curie": "UMLS:C0749098", "names": ["Acute Subdural Hematoma", "acute hematoma subdural", "Acute subdural hematoma", "acute subdural hematoma", "Subdural Hematoma, Acute", "acute hematomas subdural", "Acute Subdural Hematomas", "Hematoma, Acute Subdural", "Acute subdural haematoma", "SUBDURAL HEMORRHAGE ACUTE", "Subdural Hematomas, Acute", "Hematomas, Acute Subdural", "Hematoma, Subdural, Acute", "subdural hemorrhage acute", "Hemorrhage, Subdural, Acute", "acute subdural hematoma (diagnosis)", "subdural hemorrhage acute (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hematoma, Subdural, Acute", "shortest_name_length": 23}
{"curie": "MONDO:0600011", "names": ["mild hypophosphatasia", "attenuated hypophosphatasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mild hypophosphatasia", "shortest_name_length": 21}
{"curie": "MONDO:0011912", "names": ["DFNB37", "autosomal recessive deafness 37", "deafness, autosomal recessive 37", "DEAFNESS, AUTOSOMAL RECESSIVE 37", "Deafness, Autosomal Recessive 37", "deafness, autosomal recessive type 37", "autosomal recessive nonsyndromic deafness 37", "MYO6 autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 37", "autosomal recessive nonsyndromic deafness type 37", "autosomal recessive nonsyndromic deafness caused by mutation in MYO6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 37", "shortest_name_length": 6}
{"curie": "MONDO:0009810", "names": ["Petit-Fryns syndrome", "Petit Fryns syndrome", "Osteolysis syndrome recessive", "osteolysis syndrome recessive", "osteolysis syndrome, recessive", "Osteolysis Syndrome, Recessive", "OSTEOLYSIS SYNDROME, RECESSIVE", "Autosomal recessive distal osteolysis syndrome", "autosomal recessive distal osteolysis syndrome", "Autosomal recessive distal osteolysis syndrome (disorder)", "autosomal recessive distal osteolysis syndrome (diagnosis)", "Distal osteolysis, short stature and intellectual disability", "distal osteolysis-short stature-intellectual disability syndrome", "Distal osteolysis-short stature-intellectual disability syndrome", "Osteolysis, distal, with short stature, mental retardation, and characteristic facial appearance", "osteolysis, distal, with short stature, mental retardation, and characteristic Facial appearance", "OSTEOLYSIS, DISTAL, WITH SHORT STATURE, MENTAL RETARDATION, AND CHARACTERISTIC FACIAL APPEARANCE", "osteolysis, distal, with short stature, mental retardation, and characteristic facial appearance", "osteolysis, distal, with short stature, intellectual disability, and characteristic facial appearance", "osteolysis, distal, with short stature, intellectual disability, and characteristic Facial appearance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive distal osteolysis syndrome", "shortest_name_length": 20}
{"curie": "MONDO:0018755", "names": ["scorpion envenomation", "poisoning due to scorpion venom", "Poisoning due to scorpion venom", "Toxic effect of venom of scorpion", "toxic effect of venom of scorpion", "Poisoning caused by scorpion venom", "poisoning caused by scorpion venom", "Toxic effect of venom of scorpion NOS", "Poisoning caused by scorpion venom (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scorpion envenomation", "shortest_name_length": 21}
{"curie": "MONDO:0019927", "names": ["somatotropinoma", "Somatotropinoma", "Somatotrophinoma", "somatotroph tumor", "somatotroph neoplasm", "Somatotropic adenoma", "pituitary somatotropinoma", "somatotropinoma of pituitary", "growth hormone producing tumor", "pituitary gland somatotropinoma", "somatotropinoma of the pituitary", "somatotropinoma of pituitary gland", "somatotropinoma of the pituitary gland", "Growth hormone-producing pituitary tumor", "growth hormone-producing pituitary tumor", "growth hormone producing pituitary tumor", "growth hormone secreting pituitary tumor", "pituitary tumor, growth hormone producing", "Growth hormone-producing pituitary tumour", "growth hormone producing pituitary neoplasm", "growth hormone producing tumor of pituitary", "growth hormone secreting pituitary neoplasm", "growth hormone secreting tumor of pituitary", "Growth hormone-producing pituitary gland tumor", "growth hormone secreting pituitary gland tumor", "growth hormone producing neoplasm of pituitary", "growth hormone secreting neoplasm of pituitary", "growth hormone producing pituitary gland tumor", "growth hormone secreting tumor of the pituitary", "growth hormone producing tumor of the pituitary", "growth hormone secreting pituitary gland neoplasm", "growth hormone-producing pituitary gland neoplasm", "growth hormone producing tumor of pituitary gland", "Growth Hormone-Producing Pituitary Gland Neoplasm", "growth hormone producing pituitary gland neoplasm", "growth hormone secreting tumor of pituitary gland", "growth hormone secreting neoplasm of the pituitary", "growth hormone producing neoplasm of the pituitary", "growth hormone secreting neoplasm of pituitary gland", "growth hormone producing neoplasm of pituitary gland", "growth hormone producing tumor of the pituitary gland", "growth hormone secreting tumor of the pituitary gland", "growth hormone secreting neoplasm of the pituitary gland", "growth hormone producing neoplasm of the pituitary gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "growth hormone-producing pituitary gland neoplasm", "shortest_name_length": 15}
{"curie": "UMLS:C0266672", "names": ["Amyelencephaly", "Amyelencephalus", "amyelencephalus", "Congenital brain aplasia", "Brain aplasia, congenital", "Amyelencephalus (disorder)", "Amyelencephalus (diagnosis)", "Congenital brain aplasia (disorder)", "congenital malformation brain amyelencephalus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Amyelencephalus", "shortest_name_length": 14}
{"curie": "MONDO:0009515", "names": ["FLD", "Norum Disease", "NORUM DISEASE", "Norum disease", "norum disease", "LCAT deficiency", "lcat deficiency", "LCAT DEFICIENCY", "LCAT Deficiency", "Norum's disease", "LCATA Deficiency", "Deficiency, LCAT", "LCATA Deficiencies", "alpha LCAT Deficiency", "alpha-LCAT Deficiency", "Deficiency, alpha-LCAT", "LCAT deficiency syndrome", "complete LCAT deficiency", "familial LCAT deficiency", "lecithin acyltransferase deficiency", "Lecithin Acyltransferase Deficiency", "Cholesterol ester deficiency disease", "familial cholesteryl ester deficiency", "Lecithin:Cholesterol Acyltransferase Deficiency", "Lecithin-cholesterol acyltransferase deficiency", "LECITHIN:CHOLESTEROL ACYLTRANSFERASE DEFICIENCY", "Lecithin Cholesterol Acyltransferase Deficiency", "LECITHIN CHOLESTEROL ACYLTRANSFERASE DEFICIENCY", "Lecithin cholesterol acyltransferase deficiency", "lecithin:cholesterol acyltransferase deficiency", "lecithin cholesterol acyltransferase deficiency", "deficiency; lecithin cholesterol acyltransferase", "Acyltransferase Deficiency, Lecithin:Cholesterol", "lecithin cholesterol acyltransferase; deficiency", "Phosphatidylcholine-sterol acyltransferase deficiency", "alpha-Lecithin:Cholesterol Acyltransferase Deficiency", "alpha-Lecithin-Cholesterol Acyltransferase Deficiency", "LCAT - Lecithin-cholesterol acyltransferase deficiency", "Familial lecithin-cholesterol acyltransferase deficiency", "Lecithin cholesterol acyltransferase deficiency (disorder)", "lecithin cholesterol acyltransferase deficiency (diagnosis)", "Phosphatidylcholine-sterol acyltransferase deficiency (disorder)", "Familial lecithin-cholesterol acyl transferase deficiency syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Norum disease", "shortest_name_length": 3}
{"curie": "MONDO:0017095", "names": ["FCD type I", "isolated focal cortical dysplasia type I"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated focal cortical dysplasia type I", "shortest_name_length": 10}
{"curie": "MONDO:0002849", "names": ["liver rhabdomyosarcoma", "Liver Rhabdomyosarcoma", "Hepatic Rhabdomyosarcoma", "hepatic rhabdomyosarcoma", "Rhabdomyosarcoma of Liver", "rhabdomyosarcoma of liver", "rhabdomyosarcoma of the liver", "Rhabdomyosarcoma of the Liver", "liver rhabdomyosarcoma (disease)", "rhabdomyosarcoma (disease) of liver", "rhabdomyosarcoma of liver (diagnosis)", "liver neoplasm malignant rhabdomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "liver rhabdomyosarcoma", "shortest_name_length": 22}
{"curie": "MONDO:0004417", "names": ["Nested urothelial carcinoma", "nested variant infiltrating bladder urothelial carcinoma", "infiltrating bladder urothelial carcinoma, nested variant", "Infiltrating Bladder Urothelial Carcinoma, Nested Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nested variant infiltrating bladder urothelial carcinoma", "shortest_name_length": 27}
{"curie": "UMLS:C0278713", "names": ["Stage III Wilms Tumor", "stage III Wilms tumor", "stage III Wilms' tumor", "stage III Wilm's tumor", "Wilms tumor, stage III", "Wilm's tumor, stage III", "Wilms' tumor, stage III", "stage III nephroblastoma", "nephroblastoma, stage III", "Stage III Renal Wilms Tumor", "Stage III Kidney Wilms Tumor", "Stage III Renal Wilms' Tumor", "Stage III Kidney Nephroblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Kidney Wilms Tumor", "shortest_name_length": 21}
{"curie": "MONDO:0009329", "names": ["PVOD2", "Pulmonary hemangiomas", "pulmonary venoocclusive disease 2", "PULMONARY VENOOCCLUSIVE DISEASE 2", "Pulmonary capillary hemangiomatosis", "pulmonary capillary hemangiomatosis", "Pulmonary capillary haemangiomatosis", "familial pulmonary capillary hemangiomatosis", "FAMILIAL PULMONARY CAPILLARY HEMANGIOMATOSIS", "Familial pulmonary capillary hemangiomatosis", "Hemangiomatosis, familial pulmonary capillary", "hemangiomatosis, familial pulmonary capillary", "Familial pulmonary capillary haemangiomatosis", "HEMANGIOMATOSIS, FAMILIAL PULMONARY CAPILLARY", "Pulmonary capillary hemangiomatosis (disorder)", "PULMONARY VENOOCCLUSIVE DISEASE 2, AUTOSOMAL RECESSIVE", "pulmonary venoocclusive disease 2, autosomal recessive", "Familial pulmonary capillary hemangiomatosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary venoocclusive disease 2", "shortest_name_length": 5}
{"curie": "MONDO:0016097", "names": ["Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier", "Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers", "symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers", "Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers", "shortest_name_length": 79}
{"curie": "MONDO:0016146", "names": ["caveolinopathy", "qualitative or quantitative defects of caveolin-3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "caveolinopathy", "shortest_name_length": 14}
{"curie": "MONDO:0019296", "names": ["superficial fascia disease", "Subcutaneous tissue disease", "subcutaneous tissue disorder", "disease of superficial fascia", "disorder of superficial fascia", "Disorder of subcutaneous tissue", "superficial fascia disease or disorder", "disease or disorder of superficial fascia", "Disorder of subcutaneous tissue (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "subcutaneous tissue disorder", "shortest_name_length": 26}
{"curie": "UMLS:C3272817", "names": ["Rectal Micropapillary Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rectal Micropapillary Adenocarcinoma", "shortest_name_length": 36}
{"curie": "UMLS:C1261958", "names": ["Respiratory tract infection fungal", "fungal respiratory tract infection", "respiratory tract infection fungal", "fungal respiratory tract infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Respiratory tract infection fungal", "shortest_name_length": 34}
{"curie": "MONDO:0100100", "names": ["SEPN1-related myopathy", "SELENON-related myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SELENON-related myopathy", "shortest_name_length": 22}
{"curie": "MONDO:0006770", "names": ["GCG", "CGCG", "GCLSB", "jaw; granuloma", "granuloma; jaw", "giant cell granuloma", "cell giant granuloma", "Giant Cell Granuloma", "Giant cell granuloma", "granuloma; giant cell", "Granuloma, Giant Cell", "Giant Cell Granulomas", "giant cell; granuloma", "Granulomas, Giant Cell", "Giant cell granuloma NOS", "Giant cell granuloma, NOS", "central giant cell granuloma", "Central Giant Cell Granuloma", "Central giant cell granuloma", "Giant cell granuloma, central", "cell central giant granulomas", "Giant Cell Reparative Granuloma", "Giant cell reparative granuloma", "giant cell reparative granuloma", "giant cell lesion of small bones", "Granuloma, Giant Cell Reparative", "Giant Cell Lesion of Small Bones", "CGCG - Central giant cell granuloma", "Central giant cell reparative granuloma", "Central giant cell (reparative) granuloma", "central giant cell (reparative) granuloma", "granuloma; jaw (bone), giant cell, reparative", "jaw (bone); granuloma, giant cell, reparative", "Giant cell granuloma (morphologic abnormality)", "Central giant cell reparative granuloma of jaw", "central giant cell reparative granuloma of jaw", "Central giant cell reparative granuloma of jaw (disorder)", "central giant cell reparative granuloma of jaw (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "giant cell reparative granuloma", "shortest_name_length": 3}
{"curie": "MONDO:0017734", "names": ["sialidosis", "sialidoses", "Sialidosis", "Sialidoses", "Neu Deficiency", "NEU DEFICIENCY", "Neug Deficiency", "NEUG DEFICIENCY", "Mucolipidosis I", "mucolipidosis I", "I; mucolipidosis", "mucolipidosis; I", "Sialidosis, type 1", "Sialidosis Type II", "Sialidase deficiency", "Type I Mucolipidoses", "Mucolipidosis Type I", "Mucolipidosis type I", "SIALIDASE DEFICIENCY", "Mucolipidosis Type 1", "mucolipidosis type I", "Type I Mucolipidosis", "Mucolipidosis, type I", "Mucolipidoses, Type I", "Sialidosis (disorder)", "Mucolipidosis, Type I", "Deficiency of sialidase", "Normosomatic sialidosis", "Neuraminidase deficiency", "Neuraminidase Deficiency", "NEURAMINIDASE DEFICIENCY", "neuraminidase deficiency", "Neuroaminidase deficiency", "Deficiency of neuraminidase", "Sialidosis [mucolipidosis I]", "mucolipidosis type I (diagnosis)", "Cherry Red Spot Myoclonus Syndrome", "Deficiency of sialidase (disorder)", "Myoclonus-Cherry Red Spot Syndrome", "Cherry-red spot myoclonus syndrome", "Cherry-red-spot myoclonus syndrome", "Myoclonus Cherry Red Spot Syndrome", "Cherry Red Spot-Myoclonus Syndrome", "MYOCLONUS--CHERRY RED SPOT SYNDROME", "CHERRY RED SPOT--MYOCLONUS SYNDROME", "GLYCOPROTEIN NEURAMINIDASE DEFICIENCY", "Glycoprotein Neuraminidase Deficiency", "Deficiency, Glycoprotein Neuraminidase", "Glycoprotein Neuraminidase Deficiencies", "Deficiencies, Glycoprotein Neuraminidase"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sialidosis", "shortest_name_length": 10}
{"curie": "MONDO:0006762", "names": ["Freemartinism", "freemartinism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "freemartinism", "shortest_name_length": 13}
{"curie": "UMLS:C0272373", "names": ["Drug-induced coagulation inhibitor disorder", "Drug-induced coagulation inhibitor disorder, NOS", "Drug-induced coagulation inhibitor disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Drug-induced coagulation inhibitor disorder", "shortest_name_length": 43}
{"curie": "MONDO:0035383", "names": ["FOXG1 syndrome", "FOXG1-related epileptic-dyskinetic encephalopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FOXG1 syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0018932", "names": ["cirrhotic cardiomyopathy", "Cirrhotic cardiomyopathy", "cardiomyopathy due to cirrhosis of liver", "Cardiomyopathy due to cirrhosis of liver", "Cardiomyopathy due to cirrhosis of liver (disorder)", "cardiomyopathy due to cirrhosis of liver (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cirrhotic cardiomyopathy", "shortest_name_length": 24}
{"curie": "MONDO:0009524", "names": ["Jancar syndrome", "Mental retardation spasticity ectrodactyly", "mental retardation spasticity ectrodactyly", "intellectual disability spasticity ectrodactyly", "ectrodactyly, spastic paraplegia and mental retardation", "Ectrodactyly, spastic paraplegia and mental retardation", "Intellectual disability-spasticity-ectrodactyly syndrome", "intellectual disability-spasticity-ectrodactyly syndrome", "intellectual disability, spasticity, ectrodactyly syndrome", "Intellectual disability, spasticity, ectrodactyly syndrome", "mental retardation, spasticity and transverse limb defects", "Mental retardation, spasticity and transverse limb defects", "ectrodactyly-spastic paraplegia-mental retardation syndrome", "ectrodactyly, spastic paraplegia and intellectual disability", "intellectual disability, spasticity and transverse limb defects", "distal transverse limb defects-mental retardation-spasticity syndrome", "Intellectual disability, spasticity, ectrodactyly syndrome (disorder)", "mental retardation-spasticity-distal transverse limb defects syndrome", "intellectual disability, spasticity, ectrodactyly syndrome (diagnosis)", "limb defects, distal transverse, with mental retardation and spasticity", "Limb Defects, Distal Transverse, with Mental Retardation and Spasticity", "LIMB DEFECTS, DISTAL TRANSVERSE, WITH MENTAL RETARDATION AND SPASTICITY", "limb defects, distal transverse, with intellectual disability and spasticity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability-spasticity-ectrodactyly syndrome", "shortest_name_length": 15}
{"curie": "MONDO:0021106", "names": ["laminopathy", "Laminopathy", "Laminopathies", "LMNA-Linked Disease", "LMNA Linked Diseases", "LMNA-Linked Diseases", "Disease, LMNA-Linked", "LMNA-Associated Disease", "LMNA Associated Diseases", "LMNA-Associated Diseases", "Disease, LMNA-Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laminopathy", "shortest_name_length": 11}
{"curie": "UMLS:C2981666", "names": ["Stage IIA Distal Bile Duct Cancer", "stage IIA distal bile duct cancer", "stage IIA distal bile duct cancer AJCC v7", "Stage IIA Distal Bile Duct Cancer AJCC v7", "stage IIA distal extrahepatic bile duct cancer", "Stage IIA Extrahepatic (Distal) Bile Duct Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Distal Bile Duct Cancer AJCC v7", "shortest_name_length": 33}
{"curie": "UMLS:C4520904", "names": ["Stage 0 Squamous Cell Lung Cancer", "Lung Squamous Cell Carcinoma In Situ", "Lung Epidermoid Cell Carcinoma In Situ", "Stage 0 Epidermoid Cell Lung Carcinoma", "Squamous Cell Carcinoma In Situ of Lung", "Stage 0 Squamous Cell Carcinoma of Lung", "Stage 0 Epidermoid Cell Carcinoma of Lung", "Epidermoid Cell Carcinoma In Situ of Lung", "Stage 0 Squamous Cell Carcinoma of the Lung", "Squamous Cell Carcinoma In Situ of the Lung", "Stage 0 Squamous Cell Lung Carcinoma AJCC v6", "Stage 0 Squamous Cell Lung Carcinoma AJCC v7", "Stage 0 Epidermoid Cell Carcinoma of the Lung", "Epidermoid Cell Carcinoma In Situ of the Lung", "Stage 0 Lung Squamous Cell Carcinoma AJCC v6 and v7", "Stage 0 Squamous Cell Lung Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Squamous Cell Lung Carcinoma AJCC v6 and v7", "shortest_name_length": 33}
{"curie": "UMLS:C5419901", "names": ["Hepatobiliary Soft Tissue Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatobiliary Soft Tissue Neoplasm", "shortest_name_length": 34}
{"curie": "UMLS:C2983007", "names": ["Stage 0 Uterine Corpus Cancer", "Stage 0 Uterine Corpus Cancer AJCC v7", "Stage 0 Uterine (including Endometrial) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Uterine Corpus Cancer", "shortest_name_length": 29}
{"curie": "UMLS:C5238250", "names": ["Recurrent Oligoastrocytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Oligoastrocytoma", "shortest_name_length": 26}
{"curie": "MONDO:0019934", "names": ["polyploid", "Polyploid", "Polyploidy", "Polyploids", "polyploidy", "Polyploidies", "Polyploidy syndrome", "Polyploidy syndrome, NOS", "Polyploidy syndrome (disorder)", "Polyploidy syndrome (diagnosis)", "Polyploidy (morphologic abnormality)", "chromosomal anomalies polyploidy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyploidy", "shortest_name_length": 9}
{"curie": "UMLS:C0877107", "names": ["Sinobronchitis", "sinobronchitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinobronchitis", "shortest_name_length": 14}
{"curie": "UMLS:C5238966", "names": ["Refractory Metastatic Pancreatic Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Metastatic Pancreatic Adenocarcinoma", "shortest_name_length": 47}
{"curie": "MONDO:0011529", "names": ["SCA13", "spinocerebellar ataxia 13", "SPINOCEREBELLAR ATAXIA 13", "Spinocerebellar ataxia 13", "spinocerebellar ataxia type 13", "Spinocerebellar ataxia type 13", "SCA13 Spinocerebellar ataxia 13", "Spinocerebellar ataxia type 13 (disorder)", "Autosomal dominant cerebellar ataxia with mental retardation", "autosomal dominant cerebellar ataxia with mental retardation", "cerebellar ataxia, autosomal dominant with mental retardation", "Cerebellar ataxia, autosomal dominant with mental retardation", "autosomal dominant cerebellar ataxia with intellectual disability", "cerebellar ataxia, autosomal dominant with intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia type 13", "shortest_name_length": 5}
{"curie": "MONDO:0012084", "names": ["AADCD", "DDC deficiency", "DDC DEFICIENCY", "AADC Deficiency", "Aadc deficiency", "AADC deficiency", "AADC DEFICIENCY", "DOPA DECARBOXYLASE DEFICIENCY", "Dopa decarboxylase deficiency", "Deficiency of dopa decarboxylase", "Deficiency of tryptophan decarboxylase", "aromatic amino acid decarboxylase deficiency", "Aromatic amino acid decarboxylase deficiency", "Deficiency of hydroxytryptophan decarboxylase", "Aromatic L-Amino-Acid Decarboxylase Deficiency", "aromatic L-amino acid decarboxylase deficiency", "Aromatic L-amino acid decarboxylase deficiency", "aromatic L-amino-acid decarboxylase deficiency", "AROMATIC L-AMINO ACID DECARBOXYLASE DEFICIENCY", "Deficiency of aromatic-L-amino-acid decarboxylase", "Aromatic amino acid decarboxylase deficiency (disorder)", "aromatic L-amino acid decarboxylase deficiency (diagnosis)", "Deficiency of aromatic-L-amino-acid decarboxylase (disorder)", "AADC deficiency Aromatic L-amino acid decarboxylase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aromatic L-amino acid decarboxylase deficiency", "shortest_name_length": 5}
{"curie": "MONDO:0030072", "names": ["DEE88", "EIEE88", "early infantile epileptic encephalopathy 88", "developmental and epileptic encephalopathy 88", "DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 88", "epileptic encephalopathy, early infantile, 88", "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 88", "developmental and epileptic encephalopathy, 88"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "developmental and epileptic encephalopathy, 88", "shortest_name_length": 5}
{"curie": "MONDO:0022941", "names": ["deafness hypospadias metacarpal and metatarsal syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness hypospadias metacarpal and metatarsal syndrome", "shortest_name_length": 55}
{"curie": "UMLS:C5553005", "names": ["Borderline Ovarian Endometrioid Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Borderline Ovarian Endometrioid Tumor", "shortest_name_length": 37}
{"curie": "MONDO:0006071", "names": ["adenofibroma", "Adenofibroma", "adenofibromas", "Adenofibromas", "Adenofibroma NOS", "Adenofibroma, NOS", "Benign adenofibroma", "[M]Adenofibroma NOS", "ADENOFIBROMA, BENIGN", "adenofibroma, benign", "benign mixed Muellerian tumor", "Benign Mixed Muellerian Tumor", "adenofibroma, no ICD-O subtype", "Female Reproductive System Adenofibroma", "female reproductive system adenofibroma", "Benign adenofibroma (morphologic abnormality)", "adenofibroma, no ICD-O subtype (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adenofibroma", "shortest_name_length": 12}
{"curie": "MONDO:0012190", "names": ["EBS7", "NEPHROPATHY WITH PRETIBIAL EPIDERMOLYSIS BULLOSA AND DEAFNESS", "nephropathy with pretibial epidermolysis bullosa and deafness", "Nephropathy with Pretibial Epidermolysis Bullosa and Deafness", "EPIDERMOLYSIS BULLOSA SIMPLEX 7, WITH NEPHROPATHY AND DEAFNESS", "epidermolysis bullosa simplex 7, with nephropathy and deafness", "nephrotic syndrome - deafness - pretibial epidermolysis bullosa syndrome", "nephrotic syndrome-hearing loss-pretibial epidermolysis bullosa syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephrotic syndrome - deafness - pretibial epidermolysis bullosa syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0013563", "names": ["MCAHS1", "GPIBD3", "PIGN-CDG", "inherited GPI anchor-deficiency", "PIGN-related inherited GPI deficiency", "glycosylphosphatidylinositol biosynthesis defect 3", "GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 3", "Glycosylphosphatidylinositol Biosynthesis Defect 3", "multiple congenital anomalies-hypotonia-seizures syndrome", "congenital disorder of glycosylation due to PIGN deficiency", "Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 1", "MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1", "multiple congenital anomalies-hypotonia-seizures syndrome 1", "multiple congenital anomalies - hypotonia - seizures syndrome", "multiple congenital anomalies-hypotonia-seizures syndrome type 1", "PIGN multiple congenital anomalies/dysmorphic syndrome-intellectual disability", "multiple congenital anomalies/dysmorphic syndrome-intellectual disability caused by mutation in PIGN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple congenital anomalies-hypotonia-seizures syndrome 1", "shortest_name_length": 6}
{"curie": "UMLS:C1707791", "names": ["Disfigurement", "Deformity/ Disfigurement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disfigurement", "shortest_name_length": 13}
{"curie": "MONDO:0100138", "names": ["X-linked recessive mitochondrial myopathy", "X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked recessive mitochondrial myopathy", "shortest_name_length": 41}
{"curie": "MONDO:0001681", "names": ["Diphtheritic cystitis", "diphtheritic cystitis", "Cystitis in diphtheria", "Diphtheritic cystitis (disorder)", "diphtheritic cystitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diphtheritic cystitis", "shortest_name_length": 21}
{"curie": "MONDO:0025095", "names": ["Avian malaria", "Avian Malaria", "Malaria, Avian", "malaria, avian", "Avian Malarias", "Malarias, Avian", "Avian malaria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malaria, avian", "shortest_name_length": 13}
{"curie": "MONDO:0009704", "names": ["CPT2, myopathic form", "CPTII, myopathic form", "CPT2, adult-onset form", "CPTII, adult-onset form", "Cpt2 deficiency, late-onset", "CPT2 Deficiency, Late-Onset", "CPT 2 deficiency, myopathic", "CPT2 DEFICIENCY, LATE-ONSET", "CPT II DEFICIENCY, MYOPATHIC", "CPT II Deficiency, Myopathic", "CPT II deficiency, myopathic, stress-induced", "Carnitine Palmitoyltransferase 2 deficiency, myopathic", "Carnitine Palmitoyltransferase II Deficiency, Myopathic", "CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, MYOPATHIC", "Carnitine Palmitoyltransferase II Deficiency, Late-Onset", "CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET", "Carnitine Palmitoyltransferase 2 deficiency, adult-onset", "CARNITINE PALMITOYLTRANSFERASE II deficiency, late-onset", "CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ADULT-ONSET", "Carnitine Palmitoyltransferase II Deficiency, Adult-Onset", "Carnitine palmitoyl transferase II deficiency, myopathic form", "carnitine palmitoyl transferase II deficiency, myopathic form", "Carnitine palmitoyl transferase II deficiency, adult-onset form", "Carnitine palmitoyl transferase deficiency type 2, myopathic form", "Carnitine palmitoyl transferase deficiency type 2, adult-onset form", "Carnitine Palmitoyltransferase 2 deficiency, myopathic, stress-induced", "CARNITINE PALMITOYLTRANSFERASE II deficiency, myopathic, stress-induced", "CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, MYOPATHIC, STRESS-INDUCED"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carnitine palmitoyl transferase II deficiency, myopathic form", "shortest_name_length": 20}
{"curie": "MONDO:0009692", "names": ["mos", "AMM", "MOS", "MMM", "CIMF", "Myelofibrosis", "MYELOFIBROSIS", "myelofibrosis", "Myelofibroses", "Myeloscleroses", "myelosclerosis", "MYELOSCLEROSIS", "Myelosclerosis", "Myelofibrosis NOS", "Myeloid Metaplasia", "Osteomyelofibrosis", "Myelofibrosis, NOS", "osteomyelofibrosis", "myeloid metaplasia", "aleukemic myelosis", "MF - Myelofibrosis", "Aleukemic myelosis", "Myeloid Metaplasias", "myelosis; aleukemic", "Myelosclerosis, NOS", "aleukemic; myelosis", "Metaplasia, Myeloid", "MYELOSIS, ALEUKEMIC", "Metaplasias, Myeloid", "fibrosis bone marrow", "BONE MARROW FIBROSIS", "MYELOSIS NONLEUKEMIC", "Nonleukemic Myelosis", "Nonleukemic Myeloses", "bone Marrow Fibrosis", "bone marrow fibrosis", "Bone Marrow Fibroses", "bone fibrosis marrow", "Bone Marrow Fibrosis", "myelofibrosis primary", "myelosis; nonleukemic", "Primary Myelofibrosis", "Myelosis non-leukemic", "Fibrosis, Bone Marrow", "Myelosis, Nonleukemic", "Myeloses, Nonleukemic", "Myelosis-non-leukemic", "Fibroses, Bone Marrow", "primary myelofibrosis", "MYELOSIS NON-LEUKEMIC", "Primary myelofibrosis", "Primary Myelofibroses", "nonleukemic; myelosis", "Myelofibroses, Primary", "MYELOSIS NON-LEUKAEMIC", "Myelosis-non-leukaemic", "Myelosis non-leukaemic", "myelofibrosis, somatic", "Myelofibrosis, Primary", "Myelofibrosis (disorder)", "myelofibrosis idiopathic", "Idiopathic Myelofibrosis", "Idiopathic myelofibrosis", "idiopathic myelofibrosis", "myelofibrosis (diagnosis)", "agnogenic myeloid metaplasia", "Agnogenic myeloid metaplasia", "Agnogenic Myeloid Metaplasia", "MYELOID METAPLASIA AGNOGENIC", "MYELOID METAPLASIA, AGNOGENIC", "myeloid metaplasia, agnogenic", "megakaryocytic myelosclerosis", "Myeloid Metaplasia, Agnogenic", "Metaplasia, Agnogenic Myeloid", "Megakaryocytic myelosclerosis", "Agnogenic Myeloid Metaplasias", "Metaplasias, Agnogenic Myeloid", "osteomyelofibrosis (diagnosis)", "Myeloid Metaplasias, Agnogenic", "myelosclerosis; megakaryocytic", "megakaryocytic; myelosclerosis", "Idiopathic Bone Marrow Fibrosis", "idiopathic bone marrow fibrosis", "Chronic idiopathic myelofibrosis", "chronic idiopathic myelofibrosis", "metaplasia myelofibrosis myeloid", "Chronic Idiopathic Myelofibrosis", "primary myelofibrosis (diagnosis)", "myeloid metaplasia; myelosclerosis", "Idiopathic myelofibrosis (chronic)", "idiopathic myelofibrosis (diagnosis)", "MYELOFIBROSIS AND MYELOID METAPLASIA", "Myelofibrosis with myeloid metaplasia", "myelofibrosis with myeloid metaplasia", "MYELOFIBROSIS WITH MYELOID METAPLASIA", "Myelofibrosis With Myeloid Metaplasia", "myelosclerosis with myeloid metaplasia", "Myelosclerosis with Myeloid Metaplasia", "Myelosclerosis with myeloid metaplasia", "myelosclerosis; with myeloid metaplasia", "MYELOID METAPLASIA PRIMARY MYELOFIBROSIS", "megakaryocytic myelosclerosis (diagnosis)", "[M]Myelosclerosis with myeloid metaplasia", "MYELOID METAPLASIA <PRIMARY MYELOFIBROSIS>", "myelofibrosis with myeloid metaplasia, somatic", "Myelosclerosis with myeloid metaplasia (disorder)", "myelofibrosis with myeloid metaplasia (diagnosis)", "myelosclerosis with myeloid metaplasia (diagnosis)", "myelofibrosis/sclerosis with myeloid metaplasia (MMM)", "Myelofibrosis as a result of myeloproliferative disease", "Myelosclerosis with myeloid metaplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary myelofibrosis", "shortest_name_length": 3}
{"curie": "MONDO:0001909", "names": ["rta", "RTA, NOS", "Renotubular acidemia", "Renotubular acidaemia", "renal tubule acidosis", "ACIDOSIS RENAL TUBULAR", "acidosis tubular renal", "RENAL TUBULAR ACIDOSIS", "Renal Tubular Acidosis", "acidosis renal tubules", "RENAL ACIDOSIS TUBULAR", "Renal acidosis tubular", "renal tubular acidosis", "tubular renal acidosis", "Acidosis renal tubular", "Renal tubular acidosis", "Acidosis, Renal Tubular", "tubular acidosis; renal", "ACIDOSIS, RENAL, TUBULAR", "Renal tubular acidosis NOS", "Renal tubular acidosis, NOS", "RTA - Renal tubular acidosis", "ACIDOSIS, RENAL HYPERCHLOREMIC", "Renal tubular acidosis (disorder)", "renal tubular acidosis (diagnosis)", "Accumulation of acid in body due to kidney problem"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal tubular acidosis", "shortest_name_length": 3}
{"curie": "UMLS:C0016546", "names": ["Foreign body in GI tract", "Foreign body digestive system", "foreign body; digestive tract", "Foreign body in digestive tract", "Foreign Body in Digestive Tract", "Foreign body in alimentary tract", "foreign body of alimentary tract", "Foreign body of digestive structure", "Foreign body in digestive system NOS", "foreign body in the alimentary tract", "gastrointestinal tract; foreign body", "foreign body; gastrointestinal tract", "Foreign body in alimentary tract NOS", "Foreign body in digestive system, NOS", "Foreign body in alimentary tract, NOS", "Foreign Body in Gastrointestinal Tract", "Foreign body in gastrointestinal tract", "Foreign body in digestive tract (disorder)", "foreign body of alimentary tract (diagnosis)", "Foreign body in digestive system, unspecified", "Foreign body of alimentary tract, part unspecified", "Foreign body in alimentary tract, part unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Foreign Body in Digestive Tract", "shortest_name_length": 24}
{"curie": "UMLS:C5205932", "names": ["Prostate Mantle Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Mantle Cell Lymphoma", "shortest_name_length": 29}
{"curie": "UMLS:C2349426", "names": ["NDPH", "New Daily Persistent Headache", "new daily persistent headache", "New daily persistent headache", "New daily persistent headache (disorder)", "new daily persistent headache (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "New daily persistent headache", "shortest_name_length": 4}
{"curie": "UMLS:C1709659", "names": ["Primary Cutaneous Plasmablastic Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Cutaneous Plasmablastic Lymphoma", "shortest_name_length": 40}
{"curie": "UMLS:C4744427", "names": ["Advanced Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Neuroendocrine Carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0025193", "names": ["OPDM", "FOLP-DR", "Oculopharyngodistal myopathy", "Oculopharyngodistal Myopathy", "OCULOPHARYNGODISTAL MYOPATHY", "oculopharyngodistal myopathy", "oculopharyngeal distal myopathy", "Oculopharyngeal distal myopathy", "OPDM - oculopharyngodistal myopathy", "Oculopharyngodistal myopathy (disorder)", "oculopharyngodistal myopathy (diagnosis)", "FACIOOCULOLARYNGOPHARYNGEAL MYOPATHY WITH DISTAL AND RESPIRATORY INVOLVEMENT", "faciooculolaryngopharyngeal myopathy with distal and respiratory involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculopharyngodistal myopathy", "shortest_name_length": 4}
{"curie": "MONDO:0012818", "names": ["MODY9", "MODY type 9", "MODY PAX4 related", "diabetes mellitus MODY type 9", "maturity-onset diabetes of the young type 9", "type 9 maturity-onset diabetes of the young", "maturity-onset diabetes of the young, type 9", "MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 9", "Maturity-Onset Diabetes Of The Young, Type 9", "Maturity-onset diabetes of the young, type 9", "maturity-onset diabetes of the young - type 9", "maturity-onset diabetes of the young, type IX", "PAX4 maturity-onset diabetes of the young (disease)", "MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 9 (disorder)", "Maturity-onset diabetes of the young, type 9 (disorder)", "maturity-onset diabetes of the young - type 9 (diagnosis)", "maturity-onset diabetes of the young (disease) caused by mutation in PAX4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maturity-onset diabetes of the young type 9", "shortest_name_length": 5}
{"curie": "MONDO:0017277", "names": ["partial monosomy of chromosome 12", "partial deletion of chromosome 12", "partial deletion of chromosome type 12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of chromosome 12", "shortest_name_length": 33}
{"curie": "MONDO:0054725", "names": ["SPGF21", "spermatogenic failure 21", "SPERMATOGENIC FAILURE 21"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 21", "shortest_name_length": 6}
{"curie": "UMLS:C0751918", "names": ["Cockayne Pelizaeus Merzbacher Disease", "Cockayne-Pelizaeus-Merzbacher Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cockayne-Pelizaeus-Merzbacher Disease", "shortest_name_length": 37}
{"curie": "UMLS:C5238388", "names": ["Resectable Colon Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Resectable Colon Carcinoma", "shortest_name_length": 26}
{"curie": "MONDO:0013131", "names": ["Pkd2", "PKD2", "Apkd2", "APKD2", "Polycystic Kidney Disease 2", "polycystic kidney disease 2", "POLYCYSTIC KIDNEY DISEASE 2", "polycystic kidney disease type 2", "Polycystic Kidney Disease, Type 2", "Polycystic kidney disease, type 2", "PKD2 - Polycystic kidney disease 2", "Adult Polycystic Kidney Disease Type 2", "Polycystic Kidney Disease, Adult Type 2", "polycystic kidney disease, adult, type 2", "Polycystic Kidney Disease, Adult, Type II", "POLYCYSTIC KIDNEY DISEASE, ADULT, TYPE II", "polycystic kidney disease, adult, type II", "Adult type polycystic kidney disease type 2", "Adult type polycystic kidney disease type II", "PKD2 autosomal dominant polycystic kidney disease", "Autosomal Dominant Polycystic Kidney Disease Type 2", "Autosomal dominant polycystic kidney disease type 2", "Polycystic Kidney, Type 2 Autosomal Dominant Disease", "Adult type polycystic kidney disease type 2 (disorder)", "POLYCYSTIC KIDNEY DISEASE 2 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE", "polycystic kidney disease 2 with or without polycystic liver disease", "autosomal dominant polycystic kidney disease caused by mutation in PKD2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polycystic kidney disease 2", "shortest_name_length": 4}
{"curie": "MONDO:0004552", "names": ["microinvasive cervical squamous cell carcinoma", "Microinvasive Cervical Squamous Cell Carcinoma", "Early Invasive Cervical Squamous Cell Carcinoma", "early invasive cervical squamous cell carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microinvasive cervical squamous cell carcinoma", "shortest_name_length": 46}
{"curie": "MONDO:0006966", "names": ["Secondary parkinsonism", "Secondary Parkinsonism", "parkinsonism secondary", "secondary parkinsonism", "secondary Parkinsonism", "Parkinsonism, secondary", "parkinsonism; secondary", "Parkinsonism, Secondary", "secondary; parkinsonism", "Symptomatic Parkinsonism", "symptomatic parkinsonism", "Symptomatic parkinsonism", "Parkinsonism, Symptomatic", "secondary Parkinson disease", "Secondary Parkinson disease", "Secondary Parkinson Disease", "Parkinson Disease, Secondary", "Paralysis agitans, secondary", "Symptomatic Parkinson Disease", "Secondary Parkinson's disease", "parkinson's disease secondary", "Parkinson Disease, Symptomatic", "Symptomatic Parkinson's disease", "Secondary parkinsonism (disorder)", "secondary Parkinsonism (diagnosis)", "Secondary parkinsonism, unspecified", "secondary parkinsonism, unspecified", "Symptomatic parkinsonism (disorder)", "secondary parkinsonism (disorder) [ambiguous]", "disorder presenting primarily with parkinsonism", "Disorders presenting primarily with parkinsonism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "secondary Parkinson disease", "shortest_name_length": 22}
{"curie": "MONDO:0017975", "names": ["Sex Chromosome DSD", "Sex chromosome DSD", "Sex Chromosome DSDs", "DSD, Sex Chromosome", "Chromosome DSD, Sex", "DSDs, Sex Chromosome", "Chromosome DSDs, Sex", "Sex chromosome disorder of sex development", "sex chromosome disorder of sex development", "Sex Chromosome Disorders of Sex Development"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sex chromosome disorder of sex development", "shortest_name_length": 18}
{"curie": "UMLS:C0233494", "names": ["Tense", "tension", "Tension", "TENSION", "tensions", "Tense Feeling", "Mental tension", "tension; mental", "mental; tension", "Tension (finding)", "state; tension state"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tension", "shortest_name_length": 5}
{"curie": "UMLS:C0238254", "names": ["Secondary Lung Cancer", "Secondary Lung Carcinoma", "LUNG, SECONDARY CARCINOMA", "LUNG, CARCINOMA, METASTATIC", "Metastatic Carcinoma in the Lung", "Metastatic Carcinoma to the Lung", "LUNG CANCER, METASTATIC CARCINOMA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Carcinoma in the Lung", "shortest_name_length": 21}
{"curie": "UMLS:C5206631", "names": ["Non-HPV-Related PeIN", "Non-Human Papillomavirus-Related PeIN", "Non-Human Papillomavirus-Related Penile Intraepithelial Neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Human Papillomavirus-Related Penile Intraepithelial Neoplasia", "shortest_name_length": 20}
{"curie": "UMLS:C5204271", "names": ["Kidney Neuroendocrine Tumor", "Kidney Well-Differentiated Neuroendocrine Tumor", "Kidney Well Differentiated Neuroendocrine Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kidney Neuroendocrine Tumor", "shortest_name_length": 27}
{"curie": "MONDO:0019568", "names": ["EDS II", "EDSCL2", "EDS2, FORMERLY", "EDS II, formerly", "EDS II, FORMERLY", "Ehlers-Danlos syndrome type 2", "Ehlers-Danlos syndrome, mitis", "Ehlers-Danlos syndrome type II", "Ehlers-Danlos syndrome, type 2", "type II Ehlers-Danlos syndrome", "Ehlers-Danlos syndrome, type II", "Ehlers-Danlos Syndrome, Type II", "Ehlers-Danlos syndrome, type Ii", "Ehlers-Danlos syndrome, MITIS type", "Ehlers Danlos syndrome, mitis type", "Cutis hyperelastica II, mitis type", "Ehlers Danlos Syndrome, MITIS Type", "Ehlers-Danlos syndrome classic type 2", "Ehlers-Danlos syndrome, classic type, 2", "EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 2", "Ehlers-Danlos syndrome, type 2 (disorder)", "EHLERS-DANLOS SYNDROME, TYPE II, FORMERLY", "Ehlers Danlos Syndrome, Mild Classic Type", "Ehlers-Danlos syndrome, mild classic form", "Ehlers-Danlos syndrome, mild classic type", "Ehlers Danlos syndrome, mild Classic type", "Ehlers-Danlos syndrome, type Ii, formerly", "Ehlers-Danlos syndrome, type II (diagnosis)", "EHLERS DANLOS SYNDROME, MITIS TYPE, FORMERLY", "Ehlers Danlos syndrome, mitis type, formerly", "Ehlers Danlos syndrome, mild Classic type, formerly", "EHLERS DANLOS SYNDROME, MILD CLASSIC TYPE, FORMERLY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ehlers-Danlos syndrome, classic type, 2", "shortest_name_length": 6}
{"curie": "UMLS:C4521790", "names": ["IIIA", "Stage IIIA Gastric (Stomach) Cancer", "Pathologic Stage IIIA Gastric Cancer AJCC v8", "Pathologic Stage IIIA Gastric Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IIIA Gastric Cancer AJCC v8", "shortest_name_length": 4}
{"curie": "MONDO:0003083", "names": ["vein; anomaly", "anomaly; vein", "Venous angioma", "Venous Angioma", "vein; deformity", "deformity; vein", "venous hemangioma", "Venous hemangioma", "hemangioma venous", "Venous Hemangioma", "hemangioma; venous", "Venous haemangioma", "hemangiomas venous", "venous; hemangioma", "Venous malformation", "Venous Malformation", "MALFORMATION VENOUS", "Venous malformations", "Venous malformation NOS", "Venous hemangioma (disorder)", "Venous malformation (disorder)", "Venous hemangioma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "venous hemangioma", "shortest_name_length": 13}
{"curie": "UMLS:C0262382", "names": ["Atrial bigeminy", "atrial bigeminy", "Atrial Bigeminy", "ATRIAL BIGEMINY", "bigeminal rhythm atrial", "Atrial bigeminy (disorder)", "Atrial bigeminy (diagnosis)", "Atrial Bigeminy by EKG Finding", "Atrial Bigeminy by ECG Finding"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atrial bigeminy", "shortest_name_length": 15}
{"curie": "MONDO:0010757", "names": ["widow's peak syndrome", "WIDOW'S PEAK SYNDROME", "Widow's Peak Syndrome", "Widow's Peak, Ptosis, and Skeletal Anomalies", "WIDOW'S PEAK, PTOSIS, AND SKELETAL ANOMALIES", "widow's peak, ptosis, and skeletal anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "widow's peak syndrome", "shortest_name_length": 21}
{"curie": "MONDO:0007236", "names": ["BOR1", "Melnick-Fraser syndrome", "branchiootorenal dysplasia", "BRANCHIOOTORENAL SYNDROME 1", "Branchiootorenal Syndrome 1", "branchiootorenal syndrome 1", "branchiootorenal syndrome type 1", "branchiootorenal syndrome 1, with or without cataracts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "branchiootorenal syndrome 1", "shortest_name_length": 4}
{"curie": "MONDO:0023039", "names": ["eccrine mucinous carcinoma", "Mucinous eccrine carcinoma", "Primary mucinous carcinoma of skin", "Mucinous eccrine carcinoma of skin", "Mucinous eccrine carcinoma of skin (disorder)", "Mucinous eccrine carcinoma of skin (diagnosis)", "Mucinous eccrine carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "eccrine mucinous carcinoma", "shortest_name_length": 26}
{"curie": "UMLS:C1332344", "names": ["Atrial Septum Lipomatous Hypertrophy", "Massive Fatty Deposits of Atrial Septum", "Interatrial Septum Lipomatous Hypertrophy", "Massive Fatty Deposits of the Atrial Septum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atrial Septum Lipomatous Hypertrophy", "shortest_name_length": 36}
{"curie": "MONDO:0012142", "names": ["OFC5", "Orofacial Cleft 5", "OROFACIAL CLEFT 5", "orofacial cleft 5", "MSX1 orofacial cleft", "orofacial cleft type 5", "orofacial cleft caused by mutation in MSX1", "nonsyndromic cleft lip with or without cleft palate 5", "CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 5", "Cleft Lip with or without Cleft Palate, Nonsyndromic, 5", "cleft lip with or without cleft palate, nonsyndromic, 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orofacial cleft 5", "shortest_name_length": 4}
{"curie": "UMLS:C4329266", "names": ["Acute Megakaryoblastic Leukemia with CBFA2T3-GLIS2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Megakaryoblastic Leukemia with CBFA2T3-GLIS2", "shortest_name_length": 50}
{"curie": "MONDO:0016239", "names": ["CYSTINOSIS", "cystinosis", "Cystinosis", "Cystinoses", "Cystinosis, NOS", "cystine disease", "Cystine Disease", "Cystine disease", "Cystine Diseases", "Cystine diathesis", "cystine diathesis", "Cystine Diatheses", "Cystine Diathesis", "Diathesis, Cystine", "Diatheses, Cystine", "Defect of Cystinosin", "CYSTINOSIN, DEFECT OF", "Cystinosin, Defect of", "Cystinosis (disorder)", "cystinosis (diagnosis)", "Cystine storage disease", "Cystine Storage Disease", "cystine storage disease", "Storage Disease, Cystine", "Cystine Storage Diseases", "cystine; storage disease", "Storage Diseases, Cystine", "Fanconi's syndrome, childhood type", "Protein defect of cystin transport", "Lysosomal Cystine Transport Protein, Defect Of", "LYSOSOMAL CYSTINE TRANSPORT PROTEIN, DEFECT OF"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cystinosis", "shortest_name_length": 10}
{"curie": "MONDO:0007999", "names": ["HPE2", "Holoprosencephaly 2", "holoprosencephaly 2", "HOLOPROSENCEPHALY 2", "SIX3 holoprosencephaly", "Holoprosencephaly Type 2", "holoprosencephaly type 2", "HOLOPROSENCEPHALY 2 (disorder)", "holoprosencephaly caused by mutation in SIX3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "holoprosencephaly 2", "shortest_name_length": 4}
{"curie": "MONDO:0008164", "names": ["OTS", "OTSC1", "otosclerosis 1", "OTOSCLEROSIS 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "otosclerosis 1", "shortest_name_length": 3}
{"curie": "MONDO:0020836", "names": ["autism, susceptiblity to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autism, susceptiblity to", "shortest_name_length": 24}
{"curie": "MONDO:0006740", "names": ["empty sella", "EMPTY SELLA", "Empty Sella", "Empty sella turcica", "Empty Sella Turcica", "EMPTY SELLA TURCICA", "empty sella turcica", "empty sella syndrome", "Empty sella syndrome", "EMPTY SELLA SYNDROME", "Sella Turcica, Empty", "Empty Sella Syndrome", "Empty Sella Turcicas", "Sella Turcicas, Empty", "Empty Sella Syndromes", "Empty Sella Turcica Syndrome", "Empty sella syndrome (disorder)", "empty sella syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "empty sella syndrome", "shortest_name_length": 11}
{"curie": "UMLS:C5419773", "names": ["Appendix Neuroendocrine Tumor G3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Appendix Neuroendocrine Tumor G3", "shortest_name_length": 32}
{"curie": "MONDO:0044641", "names": ["Del(9)(q33.3q34.11)", "deletion 9q33.3q34.11", "monosomy 9q33.3q34.11", "monosomy 9q33.3-q34.11", "9q33.3q34.11 microdeletion syndrome", "9q33.3-q34.11 microdeletion syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "9q33.3q34.11 microdeletion syndrome", "shortest_name_length": 19}
{"curie": "UMLS:C5237060", "names": ["Refractory Endometrial Adenocarcinoma", "Refractory Endometrial Adenocarcinoma, NOS", "Refractory Endometrial Adenocarcinoma, Not Otherwise Specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Endometrial Adenocarcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0020543", "names": ["theca (steroid-producing) cell cancer, not further specified", "theca steroid-producing cell malignant tumor of ovary, not further specified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "theca steroid-producing cell malignant tumor of ovary, not further specified", "shortest_name_length": 60}
{"curie": "MONDO:0021644", "names": ["ESOPHAGEAL VARIX WITHOUT BLEEDING", "esophageal varices without bleeding", "Esophageal varices without bleeding", "Oesophageal varices without bleeding", "Esophageal varices without bleeding (disorder)", "Esophageal varices without mention of bleeding", "Oesophageal varices without mention of bleeding"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophageal varices without bleeding", "shortest_name_length": 33}
{"curie": "UMLS:C1609496", "names": ["Eyelid exfoliation", "exfoliation on eyelid", "exfoliation on eyelid (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eyelid exfoliation", "shortest_name_length": 18}
{"curie": "MONDO:0019531", "names": ["HEMOLYTIC ANEMIA DUE TO GLUTATHIONE REDUCTASE DEFICIENCY", "Hemolytic anemia due to glutathione reductase deficiency", "hemolytic anemia due to glutathione reductase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemolytic anemia due to glutathione reductase deficiency", "shortest_name_length": 56}
{"curie": "MONDO:0001916", "names": ["Enteric tularemia", "enteric tularemia", "Enteric tularaemia", "Intestinal tularemia", "Intestinal tularaemia", "intestinal tularaemia", "Other specified tularemia", "gastrointestinal tularemia", "Other specified tularaemia", "enteric tularemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gastrointestinal tularemia", "shortest_name_length": 17}
{"curie": "MONDO:0017936", "names": ["benign Samaritan congenital myopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign Samaritan congenital myopathy", "shortest_name_length": 36}
{"curie": "MONDO:0002716", "names": ["Spinal Cord Tumor", "Spinal cord tumor, child", "Childhood Spinal Cord Tumor", "childhood spinal cord tumor", "childhood Spinal Cord neoplasm", "childhood spinal cord neoplasm", "Childhood Spinal Cord Neoplasm", "pediatric spinal cord neoplasm", "spinal cord neoplasm of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood spinal cord tumor", "shortest_name_length": 17}
{"curie": "UMLS:C3899280", "names": ["Early Localized Lyme Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Early Localized Lyme Disease", "shortest_name_length": 28}
{"curie": "UMLS:C0431336", "names": ["Cervical myelocele", "Cervical Myelocele", "Cervical myelocele (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical myelocele", "shortest_name_length": 18}
{"curie": "MONDO:0011642", "names": ["CrAT", "Acetyl-carnitine deficiency", "acetyl-carnitine deficiency", "CARNITINE ACETYLTRANSFERASE DEFICIENCY", "Carnitine Acetyltransferase Deficiency", "carnitine acetyltransferase deficiency", "Deficiency of carnitine acetyltransferase", "Deficiency of carnitine acetyltransferase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carnitine acetyltransferase deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0006484", "names": ["UDH", "Usual Ductal Breast Hyperplasia", "Breast Usual Ductal Hyperplasia", "usual ductal breast hyperplasia", "Breast Hyperplasia without Atypia", "Usual ductal hyperplasia of breast", "Usual hyperplasia of lactiferous duct", "ordinary intraductal breast hyperplasia", "ductal breast hyperplasia of usual type", "Ordinary Intraductal Breast Hyperplasia", "Ductal Breast Hyperplasia of Usual Type", "Usual hyperplasia of lactiferous duct (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "usual ductal breast hyperplasia", "shortest_name_length": 3}
{"curie": "MONDO:0011142", "names": ["ATCS", "MCEDS", "mcEDS", "EDSmc", "EDSMC", "EDSMC1", "Dundar syndrome", "EDS, Kosho type", "EDS6B, FORMERLY", "DUNDAR SYNDROME", "EDS6B, formerly", "Dündar syndrome", "CHST14-related EDS", "D4ST1-deficient EDS", "musculocontractural EDS", "Musculocontractural EDS", "EDS, arthrogryposic type", "Adducted thumbs Dundar type", "adducted thumbs Dundar type", "EDS, musculocontractural type", "Ehlers-Danlos syndrome, type Vib", "adducted thumb-clubfoot syndrome", "ADDUCTED THUMB-CLUBFOOT SYNDROME", "Adducted Thumb-Clubfoot Syndrome", "Adducted thumb-clubfoot syndrome", "adducted thumb clubfoot syndrome", "adducted thumb-club foot syndrome", "Ehlers-Danlos syndrome Kosho type", "Ehlers-Danlos syndrome, Kosho type", "CHST14-related Ehlers-Danlos syndrome", "D4ST1-deficient Ehlers-Danlos syndrome", "Musculocontractural Ehlers-Danlos syndrome", "Ehlers-Danlos syndrome, type VIB, formerly", "musculocontractural Ehlers-Danlos syndrome", "Ehlers-Danlos syndrome arthrogryposic type", "EHLERS-DANLOS SYNDROME, TYPE VIB, FORMERLY", "Ehlers-Danlos syndrome, type Vib, formerly", "Ehlers-Danlos syndrome, arthrogryposic type", "Ehlers-Danlos syndrome musculocontractural type", "Ehlers-Danlos syndrome, musculocontractural type", "Ehlers-Danlos Syndrome, musculocontractural type 1", "EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 1", "Ehlers-Danlos syndrome, musculocontractural type 1", "Ehlers-Danlos Syndrome, Musculocontractural Type 1", "Ehlers-Danlos syndrome, musculocontractural type, 1", "EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1", "adducted thumbs-arthrogryposis syndrome, Dundar type", "autosomal recessive adducted thumb-club foot syndrome", "Adducted thumbs, arthrogryposis syndrome, Dundar type", "Ehlers-Danlos syndrome musculocontractural type (disorder)", "Distal arthrogryposis with peculiar facies and hydronephrosis", "ARTHROGRYPOSIS, DISTAL, WITH PECULIAR FACIES AND HYDRONEPHROSIS", "arthrogryposis, distal, with peculiar facies and hydronephrosis", "Arthrogryposis, Distal, With Peculiar Facies And Hydronephrosis", "ADDUCTED THUMB, CLUBFOOT, AND PROGRESSIVE JOINT AND SKIN LAXITY SYNDROME", "adducted thumb, clubfoot, and progressive joint and skin laxity syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ehlers-Danlos syndrome, musculocontractural type", "shortest_name_length": 4}
{"curie": "UMLS:C1335939", "names": ["Secondary Heart Lymphoma", "Secondary Cardiac Lymphoma", "Secondary Lymphoma in the Heart", "Metastatic Lymphoma in the Heart"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Secondary Heart Lymphoma", "shortest_name_length": 24}
{"curie": "MONDO:0007800", "names": ["18p-", "monosomy 18p", "18p monosomy", "18P Syndrome", "Monosomy 18p", "18p syndrome", "syndrome 18p", "18p- syndrome", "18p- SYNDROME", "Del(18p) syndrome", "monosomy type 18p", "del(18p) syndrome", "18p minus syndrome", "De Grouchy syndrome", "partial monosomy 18p", "Deletion 18p Syndrome", "18p deletion syndrome", "de Grouchy syndrome 1", "deletion 18p syndrome", "Deletion 18p syndrome", "chromosome 18p monosomy", "chromosome 18p deletion", "chromosome 18p deletion syndrome", "Chromosome 18p deletion syndrome", "CHROMOSOME 18p DELETION SYNDROME", "Partial deletion of chromosome 18p", "Partial monosomy of chromosome 18p", "partial deletion of chromosome 18p", "partial monosomy of chromosome 18p", "deletions of short arm chromosome 18", "Deletion of short arm of chromosome 18", "deletion of short arm of chromosome 18", "Deletion of short arm of chromosome 18 (disorder)", "partial deletion of the short arm of chromosome 18", "Partial deletion of the short arm of chromosome 18", "partial monosomy of the short arm of chromosome 18", "deletion of short arm of chromosome 18 (diagnosis)", "Partial monosomy of the short arm of chromosome 18", "partial deletion of the short arm of chromosome type 18"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 18p deletion syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C1843512", "names": ["Infantile hemiparesis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infantile hemiparesis", "shortest_name_length": 21}
{"curie": "MONDO:0023263", "names": ["GAPDH deficiency", "Deficiency of triosephosphate dehydrogenase", "Glyceraldehyde-3-phosphate dehydrogenase deficiency", "glyceraldehyde-3-phosphate dehydrogenase deficiency", "Deficiency of glyceraldehyde-3-phosphate dehydrogenase", "Deficiency of glyceraldehyde-3-phosphate dehydrogenase (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glyceraldehyde-3-phosphate dehydrogenase deficiency", "shortest_name_length": 16}
{"curie": "UMLS:C0151763", "names": ["Damage liver", "Liver damage", "LIVER DAMAGE", "liver damage", "damage liver", "DAMAGE LIVER", "damage; liver", "liver; damage", "hepatic damage", "HEPATIC DAMAGE", "Hepatic damage", "hepatic cytolysis", "liver cell damage", "Liver cell damage", "Hepatic cytolysis", "LIVER CELL DAMAGE", "Liver damage, NOS", "Hepatic damage (NOS)", "HEPATIC DAMAGE (NOS)", "Hepatocellular injury", "Hepatocellular Injury", "hepatocellular damage", "HEPATOCELLULAR DAMAGE", "hepatocellular injury", "Hepatocellular damage", "damage hepatocellular", "Hepatocellular Damage", "Liver damage (disorder)", "Hepatocellular damage NOS", "Hepatocellular damage, NOS", "Hepatocellular Liver Injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Liver damage", "shortest_name_length": 12}
{"curie": "MONDO:0019018", "names": ["ASC", "TTS", "Takotsubo Syndrome", "Takotsubo syndrome", "Tako-Tsubo syndrome", "Tako-Tsubo Syndrome", "Tako tsubo syndrome", "Tako Tsubo Syndrome", "Tako-Tsubo Syndromes", "Syndrome, Tako-Tsubo", "Stress Cardiomyopathy", "stress cardiomyopathy", "Broken-heart Syndrome", "Broken Heart Syndrome", "Broken heart syndrome", "broken heart syndrome", "broken-heart syndrome", "Broken-heart syndrome", "Stress cardiomyopathy", "Ampulla cardiomyopathy", "Cardiomyopathy, Stress", "ampulla cardiomyopathy", "Takotsubo Cardiomyopathy", "Takotsubo cardiomyopathy", "Tako Tsubo Cardiomyopathy", "Tako-tsubo cardiomyopathy", "Tako-Tsubo Cardiomyopathy", "Ballooning cardiomyopathy", "Cardiomyopathy, Takotsubo", "Tako-Tsubo cardiomyopathy", "ballooning cardiomyopathy", "Apical ballooning syndrome", "Cardiomyopathy, Tako-Tsubo", "apical ballooning syndrome", "Apical Ballooning Syndrome", "acute stress cardiomyopathy", "Tako-Tsubo Cardiomyopathies", "stress-induced cardiomyopathy", "Takotsubo syndrome (diagnosis)", "transient antero-apical dyskinesia", "Takotsubo cardiomyopathy (disorder)", "Transient Apical Ballooning Syndrome", "Left ventricular ballooning syndrome", "Left Ventricular Apical Ballooning Syndrome", "left ventricular transient apical ballooning", "transient left ventricular apical ballooning syndrome", "Transient left ventricular apical ballooning syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tako-tsubo cardiomyopathy", "shortest_name_length": 3}
{"curie": "MONDO:0014762", "names": ["HTX7", "MMP21 visceral heterotaxy", "HETEROTAXY, VISCERAL, 7, AUTOSOMAL", "heterotaxy, visceral, 7, autosomal", "heterotaxy, visceral, 7, autosomal; HTX7", "visceral heterotaxy caused by mutation in MMP21"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heterotaxy, visceral, 7, autosomal", "shortest_name_length": 4}
{"curie": "UMLS:C0279591", "names": ["L3 Adult ALL", "L3 adult ALL", "ALL, L3 adult", "adult ALL, L3", "ALL, adult L3", "Burkitt Leukemia", "Adult Burkitt Leukemia", "adult Burkitt leukemia", "Adult Burkitt's Leukemia", "L3 Adult Acute Lymphocytic Leukemia", "L3 adult acute lymphocytic leukemia", "acute lymphocytic leukemia, adult L3", "L3 lymphocytic leukemia, acute adult", "adult acute lymphocytic leukemia, L3", "L3 acute lymphocytic leukemia, adult", "L3 Adult Acute Lymphoblastic Leukemia", "L3 adult acute lymphoblastic leukemia", "acute lymphoblastic leukemia, adult L3", "leukemia, adult acute lymphocytic , L3", "L3 lymphoblastic leukemia, acute adult", "L3 acute lymphoblastic leukemia, adult", "adult acute lymphoblastic leukemia, L3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Burkitt Leukemia", "shortest_name_length": 12}
{"curie": "MONDO:0008138", "names": ["Urrets Zavalia syndrome", "Urrets-Zavalia syndrome", "Orbital Margin, Hypoplasia of", "orbital margin, hypoplasia OF", "ORBITAL MARGIN, HYPOPLASIA OF", "syndromic orbital border hypoplasia", "Syndromic orbital border hypoplasia", "Syndromic hypoplasia of orbital border", "Syndromic hypoplasia of orbital border (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syndromic orbital border hypoplasia", "shortest_name_length": 23}
{"curie": "UMLS:C4525585", "names": ["Stage I Gastric Neuroendocrine Tumor", "Stage I Gastric Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Gastric Neuroendocrine Tumor AJCC v8", "shortest_name_length": 36}
{"curie": "UMLS:C3494247", "names": ["Organothiophosphonate Poisoning", "Organothiophosphonate Poisonings", "Poisoning, Organothiophosphonate", "Poisonings, Organothiophosphonate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Organothiophosphonate Poisoning", "shortest_name_length": 31}
{"curie": "MONDO:0013514", "names": ["Htss2", "HTSS2", "HYPT3", "Hypt3", "hypt3", "hypotrichosis 3", "HYPOTRICHOSIS 3", "KRT74 hypotrichosis", "hypotrichosis type 3", "HYPOTRICHOSIS SIMPLEX OF THE SCALP 2", "hypotrichosis simplex of the scalp 2", "hypotrichosis caused by mutation in KRT74"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypotrichosis 3", "shortest_name_length": 5}
{"curie": "UMLS:C1112209", "names": ["Abdominal sepsis", "abdomen infection", "abdomen infections", "Abdominal Infection", "infection abdominal", "Abdominal infection", "abdominal infection", "abdominal infections", "infection of abdomen", "Infection of abdomen", "Intraabdominal Infection", "Intra-Abdominal Infection", "intra-abdominal infection", "Intraabdominal Infections", "Infection, Intraabdominal", "Intra-abdominal infection", "Intra-Abdominal Infections", "Infections, Intraabdominal", "infections intra abdominal", "Infection, Intra-Abdominal", "Intra Abdominal Infections", "Infections, Intra-Abdominal", "Infectious disease of abdomen", "Infectious disorder of abdomen", "Abdominal infection (diagnosis)", "Infectious disease of abdomen (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abdominal Infection", "shortest_name_length": 16}
{"curie": "UMLS:C4764227", "names": ["Recurrent Fibrosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Fibrosarcoma", "shortest_name_length": 22}
{"curie": "UMLS:C1709103", "names": ["MIFS", "Myxoinflammatory fibroblastic sarcoma", "Myxoinflammatory Fibroblastic Sarcoma", "Acral Myxoinflammatory Fibroblastic Sarcoma", "Myxoinflammatory fibroblastic sarcoma (MIFS)", "Atypical myxoinflammatory fibroblastic tumor", "Atypical myxoinflammatory fibroblastic tumour", "Myxoinflammatory fibroblastic sarcoma (morphologic abnormality)", "Inflammatory Myxoid Tumor of the Soft Parts with Bizarre Giant Cells", "Inflammatory Myxohyaline Tumor of the Distal Extremities with Virocyte/Reed-Sternberg-Like Cells"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myxoinflammatory fibroblastic sarcoma", "shortest_name_length": 4}
{"curie": "MONDO:0009052", "names": ["ARCL1", "ARCL1A", "cutis laxa type IA", "cutis laxa type IA (diagnosis)", "cutis laxa autosomal recessive", "Cutis laxa, autosomal recessive", "Cutis Laxa, Autosomal Recessive", "cutis laxa, autosomal recessive", "CUTIS LAXA, AUTOSOMAL RECESSIVE", "Autosomal recessive cutis laxa type 1", "autosomal recessive cutis laxa type IA", "Cutis Laxa, Autosomal Recessive, Type I", "cutis laxa, autosomal recessive, type 1A", "CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA", "cutis laxa, autosomal recessive, type IA", "cutis laxa autosomal recessive (diagnosis)", "Cutis laxa, autosomal recessive (disorder)", "Autosomal recessive cutis laxa, pulmonary emphysema type", "Autosomal recessive cutis laxa with severe systemic involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutis laxa, autosomal recessive, type 1A", "shortest_name_length": 5}
{"curie": "MONDO:0016653", "names": ["Del(2)(q33.1)", "Monosomy 2q33.1", "monosomy 2q33.1", "2q33.1 microdeletion syndrome", "2q33.1 microdeletion syndrome (disorder)", "SATB2-associated syndrome due to a chromosomal rearrangement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "2q33.1 microdeletion syndrome", "shortest_name_length": 13}
{"curie": "UMLS:C3639957", "names": ["Intentional Trauma", "Nonaccidental Trauma", "Non-accidental Trauma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intentional Trauma", "shortest_name_length": 18}
{"curie": "MONDO:0020807", "names": ["Ovarian Sertoli-Stromal Tumor", "ovarian sertoli-stromal cell tumor", "Ovarian Sertoli-Stromal Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian sertoli-stromal cell tumor", "shortest_name_length": 29}
{"curie": "MONDO:0700147", "names": ["Canine Histiocytic Sarcoma", "canine histiocytic sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canine histiocytic sarcoma", "shortest_name_length": 26}
{"curie": "MONDO:0016602", "names": ["Citrin deficiency", "citrin deficiency", "Citrin deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "citrin deficiency", "shortest_name_length": 17}
{"curie": "MONDO:0012951", "names": ["CRCS8", "COLORECTAL CANCER, SUSCEPTIBILITY TO, 8", "colorectal cancer, susceptibility to, 8", "COLORECTAL CANCER, SUSCEPTIBILITY TO, ON CHROMOSOME 14q", "colorectal cancer, susceptibility to, on chromosome 14Q"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colorectal cancer, susceptibility to, 8", "shortest_name_length": 5}
{"curie": "MONDO:0010588", "names": ["EVRX", "EVR2", "Evrx", "FEVRX", "FEVR, X-Linked", "FEVR, X-LINKED", "Fevr, X-linked", "NDP exudative vitreoretinopathy", "X-linked exudative vitreoretinopathy 2", "exudative vitreoretinopathy 2, X-linked", "EXUDATIVE VITREORETINOPATHY 2, X-LINKED", "Exudative Vitreoretinopathy, Familial, 2", "EXUDATIVE VITREORETINOPATHY, FAMILIAL, 2", "exudative vitreoretinopathy, familial, 2", "exudative vitreoretinopathy caused by mutation in NDP", "Exudative Vitreoretinopathy, Familial, X-Linked Recessive", "exudative vitreoretinopathy 2, X-linked, X-linked recessive, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exudative vitreoretinopathy 2, X-linked", "shortest_name_length": 4}
{"curie": "MONDO:0030537", "names": ["CCHS2", "central hypoventilation syndrome, congenital, 2, and autonomic dysfunction", "CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL, 2, AND AUTONOMIC DYSFUNCTION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central hypoventilation syndrome, congenital, 2, and autonomic dysfunction", "shortest_name_length": 5}
{"curie": "UMLS:C0948296", "names": ["discomfort ear", "ear discomfort", "Ear discomfort", "discomfort ears"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ear discomfort", "shortest_name_length": 14}
{"curie": "MONDO:0018800", "names": ["HHA", "kallman syndrome", "Kallman syndrome", "Kallmann Syndrome", "kallmann syndrome", "kallmans syndrome", "Kallmann syndrome", "KALLMANN SYNDROME", "Syndrome, Kallmann", "kallmanns syndrome", "Kallmanns Syndrome", "Kallman's syndrome", "kallman's syndrome", "Kallmann's syndrome", "Kallmann's Syndrome", "kallmann's syndrome", "de morsier syndrome", "Kallmann syndrome 3", "de Morsier syndrome", "Anosmia eunuchoidism", "Syndrome, Kallmann's", "ANOSMIC HYPOGONADISM", "Anosmic Hypogonadism", "Anosmic Hypogonadisms", "Hypogonadism, Anosmic", "Hypogonadisms, Anosmic", "olfactogenital syndrome", "Olfactogenital dysplasia", "OLFACTOGENITAL DYSPLASIA", "olfactogenital dysplasia", "Hypogonadism with anosmia", "Olfacto genital dysplasia", "hypogonadism with anosmia", "Kallmann-de Morsier syndrome", "de Morsier-Gauthier syndrome", "hypogonadism-anosmia syndrome", "de Morsier-Kallman's syndrome", "Kallmann syndrome (diagnosis)", "familial hypogonadism with anosmia", "Maestre-Kallmann-de Morsier syndrome", "Hypogonadism with anosmia (disorder)", "Mastre de San Juan-Kallmann syndrome", "idiopathic hypothalamic hypogonadism", "Olfacto-genital pathological sequence", "Gonadotrophin deficiency with anosmia", "olfacto-ethmoidohypothalamic dysplasia", "olfacto-ethmoidodypothalamic dysraphia", "Dysplasia Olfactogenitalis of De Morsier", "DYSPLASIA OLFACTOGENITALIS OF DE MORSIER", "Dysplasia olfactogenitalis of de Morsier", "Hypogonadotropic Hypogonadism and Anosmia", "HYPOGONADOTROPIC HYPOGONADISM AND ANOSMIA", "hypogonadotropic hypogonadism with anosmia", "idiopathic hypothalamic hypogonadism (IHH)", "Hypogonadotropic Hypogonadism with Anosmia", "HYPOGONADISM, HYPOGONADOTROPIC, WITH ANOSMIA", "hypogonadotropic hypogonadism-anosmia syndrome", "Hypogonadotropic Hypogonadism-Anosmia Syndrome", "hyposmia-hypogonadotropic hypogonadism syndrome", "Anosmic Idiopathic Hypogonadotropic Hypogonadism", "Maestre de San Juan-Kallmann-de Morsier syndrome", "hypogonadotropic hypogonadism-anosmia (HHA) syndrome", "Congenital hypogonadotropic hypogonadism with anosmia", "congenital hypogonadotropic hypogonadism with anosmia", "congenital anosmia-hypogonadotropic hypogonadism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kallmann syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C0854864", "names": ["Stage IV T-Lymphoblastic Leukemia/Lymphoma", "Stage IV T Lymphoblastic Leukemia/Lymphoma", "Precursor T-lymphoblastic lymphoma/leukemia stage IV", "Precursor T-Lymphoblastic Lymphoma/Leukemia Stage IV", "Stage IV Precursor T-Lymphoblastic Lymphoma/Leukemia", "Precursor T-lymphoblastic lymphoma/leukaemia stage IV"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Precursor T-lymphoblastic lymphoma/leukemia stage IV", "shortest_name_length": 42}
{"curie": "MONDO:0000995", "names": ["Cavarre disease", "Periodic myotonia", "PERIODIC PARALYSIS", "paralysis periodic", "Periodic paralysis", "Paralysis periodic", "Familial myoplegia", "periodic paralysis", "periodic; paralysis", "paralysis; periodic", "Myoplegic dystrophy", "genetic periodic paralysis", "Familial Periodic Paralyses", "familial periodic paralysis", "familial periodic paralyses", "periodic familial paralysis", "Familial Periodic Paralysis", "Familial periodic paralysis", "familial paralysis periodic", "periodic paralysis familial", "Periodic Paralyses, Familial", "paralysis, familial periodic", "periodic paralysis, familial", "Paralyses, Familial Periodic", "periodic paralyses, familial", "Periodic Paralysis, Familial", "Familial recurrent paralysis", "Paralysis, Familial Periodic", "normokalemic periodic paralyses", "normokalemic periodic paralysis", "Familial periodic paralysis, NOS", "paralysis, normokalemic periodic", "periodic paralyses, normokalemic", "paralyses, normokalemic periodic", "periodic paralysis, normokalemic", "familial periodic paralysis syndrome", "Familial periodic paralysis, primary", "Familial periodic paralysis (disorder)", "hereditary periodic paralysis (disease)", "familial periodic paralysis syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial periodic paralysis", "shortest_name_length": 15}
{"curie": "MONDO:0014063", "names": ["MC3DN2", "TTC19 mitochondrial complex III deficiency", "mitochondrial Complex 3 deficiency, nuclear type 2", "mitochondrial complex III deficiency nuclear type 2", "MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2", "mitochondrial complex III deficiency, nuclear type 2", "mitochondrial complex III deficiency caused by mutation in TTC19"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex III deficiency nuclear type 2", "shortest_name_length": 6}
{"curie": "MONDO:0016643", "names": ["FND1", "Frontorhiny", "frontonasal dysplasia", "Frontonasal dysplasia", "median cleft syndrome", "frontonasal dysplasia 1", "Frontonasal Malformation", "median cleft face syndrome", "Median cleft face syndrome", "Median facial cleft syndrome", "Frontonasal dysplasia sequence", "Frontonasal dysplasia anomalad", "frontonasal dysplasia (diagnosis)", "Frontonasal dysplasia sequence (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontonasal dysplasia", "shortest_name_length": 4}
{"curie": "MONDO:0000916", "names": ["bowel; infection", "infection; bowel", "Septic enteritis", "enteritis bacterial", "bacterial enteritis", "Bacterial enteritis", "enteritis; bacterial", "bacterial; enteritis", "Intestinal infection", "infection intestinal", "intestinal infection", "intestinal infections", "infections intestinal", "Intestinal infections", "Bacterial enteritis NOS", "Bacterial enteritis, NOS", "intestinal infectious disease", "disease infectious intestines", "Intestinal infectious disease", "Intestinal infectious diseases", "INTESTINAL INFECTIOUS DISEASES", "Bacterial enteritis (diagnosis)", "Infectious disease of intestine", "Bacterial enteritis, unspecified", "Bacterial enteritis of intestine", "intestinal infections (diagnosis)", "intestinal disorder infectious disease", "Intestinal infectious diseases (A00-A09)", "Intestinal infectious disease (disorder)", "Intestinal infectious disease (diagnosis)", "Inflammation of intestine caused by bacteria", "Inflammation of intestine caused by bacteria (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intestinal infectious disease", "shortest_name_length": 16}
{"curie": "MONDO:0018929", "names": ["osteitis condensans of the clavicle", "condensing osteitis of the clavicle", "condensing osteitis of the medial clavicle", "medial condensing osteitis of the clavicle"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "medial condensing osteitis of the clavicle", "shortest_name_length": 35}
{"curie": "MONDO:0011159", "names": ["DFNA13", "autosomal dominant deafness 13", "DEAFNESS, AUTOSOMAL DOMINANT 13", "Deafness, Autosomal Dominant 13", "deafness, autosomal dominant 13", "deafness, autosomal dominant type 13", "autosomal dominant nonsyndromic deafness 13", "autosomal dominant nonsyndromic hearing loss 13", "autosomal dominant nonsyndromic deafness type 13", "COL11A2 autosomal dominant nonsyndromic deafness", "autosomal dominant nonsyndromic deafness caused by mutation in COL11A2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant nonsyndromic hearing loss 13", "shortest_name_length": 6}
{"curie": "MONDO:0018733", "names": ["intellectual disability syndrome due to a DYRK1A point mutation", "DYRK1A-related intellectual disability syndrome due to a point mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability syndrome due to a DYRK1A point mutation", "shortest_name_length": 63}
{"curie": "UMLS:C1258085", "names": ["barrett epithelium", "Barrett Epithelium", "barretts epithelium", "Epithelium, Barrett"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Barrett Epithelium", "shortest_name_length": 18}
{"curie": "MONDO:0015619", "names": ["isolated urogenital tract malformation", "nonsyndromic urogenital tract malformation", "non-syndromic urogenital tract malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-syndromic urogenital tract malformation", "shortest_name_length": 38}
{"curie": "UMLS:C4528668", "names": ["Refractory AML", "Acute myeloid leukemia refractory", "Refractory acute myeloid leukemia", "Refractory Acute Myeloid Leukemia", "Refractory acute myeloid leukaemia", "Acute myeloid leukaemia refractory", "Refractory acute myelocytic leukemia", "Refractory acute myelocytic leukaemia", "leukemia acute myeloblastic refractory", "Refractory Acute Myeloid Leukemia (AML)", "Refractory AML (acute myeloid leukemia)", "Refractory AML (acute myeloid leukaemia)", "Refractory AML (acute myelocytic leukemia)", "Refractory AML (acute myelocytic leukaemia)", "Refractory acute myeloid leukemia (disorder)", "Refractory acute myeloid leukemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory acute myeloid leukemia", "shortest_name_length": 14}
{"curie": "MONDO:0017505", "names": ["apodia, bilateral", "congenital absence of foot, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "apodia, bilateral", "shortest_name_length": 17}
{"curie": "MONDO:0027677", "names": ["isoniazid toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isoniazid toxicity", "shortest_name_length": 18}
{"curie": "MONDO:0007737", "names": ["Keutel syndrome 2", "humero-radial fusion", "Humero-radial fusion", "Ramer Ladda syndrome", "HUMERORADIAL SYNOSTOSIS", "Humeroradial synostosis", "Humeroradial Synostosis", "Humeroradial synostoses", "humeroradial synostosis", "humero-radial synostosis", "Humero-radial synostosis", "Humeral-radial synostosis", "Humeral radial synostosis", "Synostosis of radius and humerus", "Radiohumeral synostosis of elbow", "humeroradial synostosis (disease)", "Humeroradial synostosis (disorder)", "Fusion of upper and lower arm bones"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "humeroradial synostosis", "shortest_name_length": 17}
{"curie": "UMLS:C0022876", "names": ["Early Labor", "Preterm Labor", "LABOR PRETERM", "labor preterm", "Preterm labor", "preterm labor", "preterm labour", "labors preterm", "Preterm labour", "labour preterm", "Labor, Preterm", "Premature labor", "Premature Labor", "premature labor", "LABOR PREMATURE", "PREMATURE LABOR", "Labor premature", "labor premature", "premature labour", "Labour;premature", "Labor, Premature", "LABOR, PREMATURE", "Premature labour", "Labour premature", "labor; premature", "LABOUR PREMATURE", "Labor, premature", "premature; labor", "labour premature", "early onset; labor", "labor; early onset", "Premature parturition", "Premature onset of labor", "Premature labor (finding)", "Premature Obstetric Labor", "Premature onset of labour", "preterm labor (diagnosis)", "Obstetric Labor, Premature", "Labor, Premature Obstetric", "labor; premature or preterm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Premature Obstetric Labor", "shortest_name_length": 11}
{"curie": "MONDO:0011034", "names": ["Odontomicronychial dysplasia", "odontomicronychial dysplasia", "ODONTOMICRONYCHIAL DYSPLASIA", "odonto-micronychial dysplasia", "ECTODERMAL DYSPLASIA, NAIL/TOOTH TYPE", "ectodermal dysplasia, nail/Tooth type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "odontomicronychial dysplasia", "shortest_name_length": 28}
{"curie": "UMLS:C0459524", "names": ["Fallopian tube stenosis", "Fallopian Tube Stenosis", "fallopian tube; stenosis", "stenosis; fallopian tube", "stenosis of fallopian tube", "Fallopian tube stenosis (disorder)", "stenosis of fallopian tube (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fallopian tube stenosis", "shortest_name_length": 23}
{"curie": "MONDO:0009885", "names": ["SCTS", "BDPLT7", "Scott syndrome", "Scott Syndrome", "SCOTT SYNDROME", "scott syndrome", "scotts syndrome", "Scott syndrome (disorder)", "platelet-type bleeding disorder 7", "prothrombin consumption deficiency", "PROTHROMBIN CONSUMPTION DEFICIENCY", "Prothrombin Consumption Deficiency", "bleeding disorder, Platelet-type, 7", "BLEEDING DISORDER, PLATELET-TYPE, 7", "Platelet factor X receptor deficiency", "familial prothrombin conversion defect", "Prothrombin Conversion Defect, Familial", "prothrombin conversion defect, familial", "PROTHROMBIN CONVERSION DEFECT, FAMILIAL", "familial prothrombin consumption inhibitor", "prothrombin consumption inhibitor, familial", "PROTHROMBIN CONSUMPTION INHIBITOR, FAMILIAL", "Prothrombin Consumption Inhibitor, Familial", "bleeding abnormality due to deficiency of platelet biding of factor X", "BLEEDING ABNORMALITY DUE TO DEFICIENCY OF PLATELET BINDING OF FACTOR X", "Bleeding Abnormality due to Deficiency of Platelet Binding of Factor X", "bleeding Abnormality due to deficiency of Platelet binding of Factor 10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Scott syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0006179", "names": ["Desmoplastic ameloblastoma", "Desmoplastic Ameloblastoma", "desmoplastic ameloblastoma", "Desmoplastic ameloblastoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "desmoplastic ameloblastoma", "shortest_name_length": 26}
{"curie": "MESH:D020720", "names": ["Myasthenia Gravis, Autoimmune, Experimental"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Myasthenia Gravis, Autoimmune, Experimental", "shortest_name_length": 43}
{"curie": "MONDO:0019316", "names": ["UP/MPCM", "pigmentosa urticaria", "Urticaria Pigmentosa", "urticaria pigmentosa", "Urticaria pigmentosa", "URTICARIA PIGMENTOSA", "urticaria; pigmentosa", "pigmentosa; urticaria", "Urticaria pigmentosa, NOS", "Paucicellular mastocytosis", "Urticaria pigmentosa (disorder)", "urticaria pigmentosa (diagnosis)", "Localised cutaneous mastocytosis", "Localized cutaneous mastocytosis", "maculopapular cutaneous mastocytosis", "Maculopapular Cutaneous Mastocytoses", "Maculopapular cutaneous mastocytosis", "Maculopapular Cutaneous Mastocytosis", "Cutaneous Mastocytoses, Maculopapular", "Localized cutaneous mastocytosis, NOS", "MASTOCYTOSIS, MACULOPAPULAR CUTANEOUS", "Cutaneous Mastocytosis, Maculopapular", "telangiectatic cutaneous mastocytosis", "telangiectasia macularis eruptive perstans", "pigmentation; congenital, urticaria pigmentosa", "Urticaria pigmentosa (morphologic abnormality)", "maculopapular cutaneous mastocytosis (diagnosis)", "Urticaria Pigmentosa/Maculopapular Cutaneous Mastocytosis", "urticaria pigmentosa/maculopapular cutaneous mastocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maculopapular cutaneous mastocytosis", "shortest_name_length": 7}
{"curie": "MONDO:0015458", "names": ["Da Silva syndrome", "intellectual disability - hypoplastic corpus callosum - preauricular tag", "intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome", "Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome", "intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome", "Intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome", "Intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome (disorder)", "intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome", "shortest_name_length": 17}
{"curie": "MONDO:0011812", "names": ["DRRS", "DR syndrome", "DR SYNDROME", "Okihiro syndrome", "Okihiro Syndrome", "OKIHIRO SYNDROME", "Syndrome, Okihiro", "acrorenocular syndrome", "Acrorenoocular Syndrome", "Acrorenoocular syndrome", "ACRORENOOCULAR SYNDROME", "Acrorenoocular Syndromes", "Syndrome, Acrorenoocular", "Duane Radial Ray Syndrome", "Duane-Radial Ray Syndrome", "Duane-radial ray syndrome", "DUANE-RADIAL RAY SYNDROME", "Syndrome, Duane-Radial Ray", "Acro-renal-ocular syndrome", "acro-renal-ocular syndrome", "DRRS - Duane-radial ray syndrome", "Type 3 Duane Retraction Syndrome", "Duane retraction syndrome type 3", "Duane Retraction Syndrome, Type 3", "Acrorenoocular syndrome (disorder)", "Duane-radial ray syndrome (disorder)", "Duane anomaly with radial abnormalities and deafness", "Duane Anomaly with Radial Abnormalities and Deafness", "Duane Anomaly with Radial Ray Abnormalities and Deafness", "Duane anomaly with radial ray abnormalities and deafness", "DUANE ANOMALY WITH RADIAL RAY ABNORMALITIES AND DEAFNESS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Duane-radial ray syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C4744804", "names": ["Grade 1 Teratoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Grade 1 Teratoma", "shortest_name_length": 16}
{"curie": "UMLS:C0949496", "names": ["luft disease", "Luft Disease", "Disease, Luft", "lufts disease", "Lufts Disease", "luft's disease", "Luft's Disease", "Disease, Luft's"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Luft Disease", "shortest_name_length": 12}
{"curie": "UMLS:C0159776", "names": ["Closed fracture of metacarpal bone", "Closed Fracture of Metacarpal Bone", "closed fracture of metacarpal bone", "closed fracture of metacarpal bones", "Closed fracture of metacarpal bones", "Fracture of metacarpal bones, closed", "Closed fracture of metacarpal bone, NOS", "Closed fracture of metacarpal bone (disorder)", "closed fracture of metacarpal bone (diagnosis)", "Closed fracture of metacarpal bone, site unspecified", "Closed fracture of metacarpal bones, site unspecified", "Closed fracture of metacarpal bone(s), site unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Closed fracture of metacarpal bone", "shortest_name_length": 34}
{"curie": "MONDO:0009262", "names": ["GM1G3", "Adult GM1 Gangliosidosis", "Adult GM1 gangliosidosis", "adult GM1 gangliosidosis", "Gangliosidosis GM1 Type 3", "GM1 Gangliosidosis, Adult", "gangliosidosis GM1 type 3", "GM1 gangliosidosis type 3", "Gangliosidosis GM1, Adult", "Gangliosidosis, Adult GM1", "GM1 gangliosidosis, type 3", "GM1-gangliosidosis, type 3", "Gangliosidosis GM1, Type 3", "Type III GM1-Gangliosidoses", "GM1 Gangliosidosis type III", "Type III GM1-Gangliosidosis", "GM1-gangliosidosis, type III", "GM1 Gangliosidosis, Type III", "GM1-GANGLIOSIDOSIS, TYPE III", "GM1-Gangliosidoses, Type III", "gangliosidosis GM1, type III", "GM1-Gangliosidosis, Type III", "Adult-onset GM1 gangliosidosis", "gangliosidosis GM1, adult type", "adult-onset GM1 gangliosidosis", "Type 3 (Adult) GM1 Gangliosidosis", "Adult GM1 gangliosidosis (disorder)", "Beta-galactosidase deficiency type 3", "adult generalized gangliosidosis GM1", "GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 3", "Gangliosidosis, Generalized GM1, Type 3", "gangliosidosis, generalized GM1, type 3", "GM1 Gangliosidosis type III (diagnosis)", "Gangliosidosis, Generalized GM1, Type III", "GANGLIOSIDOSIS, GENERALIZED GM1, TYPE III", "gangliosidosis generalized GM1 chronic type", "generalize d gangliosidosis GM1, adult type", "gangliosidosis, generalized GM1, adult type", "Gangliosidosis, Generalized GM1, Adult Type", "GANGLIOSIDOSIS, GENERALIZED GM1, ADULT TYPE", "Gangliosidosis, Generalized GM1, Chronic Type", "gangliosidosis, generalized GM1, chronic type", "GANGLIOSIDOSIS, GENERALIZED GM1, CHRONIC TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "GM1 gangliosidosis type 3", "shortest_name_length": 5}
{"curie": "MONDO:0002961", "names": ["large cell acanthoma", "Large cell acanthoma", "Large Cell Acanthoma", "Large cell acanthoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "large cell acanthoma", "shortest_name_length": 20}
{"curie": "MONDO:0008106", "names": ["NYS2", "congenital nystagmus 2", "congenital motor nystagmus 2", "Nystagmus congenital, motor 2", "Nystagmus, congenital motor, 2", "Nystagmus, Congenital Motor, 2", "NYSTAGMUS, CONGENITAL MOTOR, 2", "autosomal dominant congenital nystagmus 2", "Nystagmus 2, congenital, autosomal dominant", "nystagmus 2, congenital, autosomal dominant", "NYSTAGMUS 2, CONGENITAL, AUTOSOMAL DOMINANT", "NYSTAGMUS 2, congenital, autosomal dominant", "NYSTAGMUS 2, CONGENITAL, AUTOSOMAL DOMINANT (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nystagmus 2, congenital, autosomal dominant", "shortest_name_length": 4}
{"curie": "MONDO:0019494", "names": ["heart tumor of child", "Cardiac tumor of child", "pediatric heart neoplasm", "primary pediatric heart tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary pediatric heart tumor", "shortest_name_length": 20}
{"curie": "MONDO:0011176", "names": ["HSH", "HOMG", "Homg", "PHSH", "HOMG1", "Grass tetany", "Grass staggers", "Hypomagnesmic tetany", "hypomagnesemic tetany", "Hypomagnesemic tetany", "HYPOMAGNESEMIC TETANY", "Hypomagnesaemic tetany", "Intestinal hypomagnesemia 1", "intestinal hypomagnesemia 1", "hypomagnesemia 1, intestinal", "TRPM6 primary hypomagnesemia", "Intestinal hypomagnesaemia 1", "HYPOMAGNESEMIA 1, INTESTINAL", "Hypomagnesemia 1, Intestinal", "intestinal hypomagnesemia type 1", "Hypomagnesemia intestinal type 1", "hypomagnesemia intestinal type 1", "Hypomagnesemic tetany (disorder)", "Hypomagnesemic tetany of ruminants", "TRPM6 familial primary hypomagnesemia", "Hypomagnesemia with secondary hypocalcemia", "hypomagnesemia with secondary hypocalcemia", "Hypomagnesemia with Secondary Hypocalcemia", "HYPOMAGNESEMIA WITH SECONDARY HYPOCALCEMIA", "Hypomagnesaemia with secondary hypocalcaemia", "Familial primary hypomagnesemia with hypocalcuria", "primary hypomagnesemia caused by mutation in TRPM6", "Familial primary hypomagnesaemia with hypocalcuria", "Primary hypomagnesemia with secondary hypocalcemia", "primary hypomagnesemia with secondary hypocalcemia", "Intestinal hypomagnesemia with secondary hypocalcemia", "Hypomagnesemia with secondary hypocalcemia (disorder)", "intestinal hypomagnesemia with secondary hypocalcemia", "Hypomagnesemia, Intestinal, with Secondary Hypocalcemia", "Intestinal hypomagnesaemia with secondary hypocalcaemia", "hypomagnesemia, intestinal, with secondary hypocalcemia", "HYPOMAGNESEMIA, INTESTINAL, WITH SECONDARY HYPOCALCEMIA", "Hypomagnesemia caused by selective magnesium malabsorption", "hypomagnesemia caused by selective magnesium malabsorption", "familial primary hypomagnesemia caused by mutation in TRPM6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intestinal hypomagnesemia 1", "shortest_name_length": 3}
{"curie": "UMLS:C1334736", "names": ["Metastatic Ovarian Small Cell Carcinoma, Hypercalcemic Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Ovarian Small Cell Carcinoma, Hypercalcemic Type", "shortest_name_length": 59}
{"curie": "UMLS:C0854388", "names": ["Caustic injury", "Caustic Injury"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Caustic injury", "shortest_name_length": 14}
{"curie": "MONDO:0006117", "names": ["breast DLBCL", "Breast DLBCL", "Breast Diffuse Large B-Cell Lymphoma", "breast diffuse large B-cell lymphoma", "diffuse large B-cell lymphoma of breast"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "breast diffuse large B-cell lymphoma", "shortest_name_length": 12}
{"curie": "MONDO:0012476", "names": ["SPG30", "hereditary spastic paraplegia 30", "KIF1A hereditary spastic paraplegia", "autosomal spastic paraplegia type 30", "Autosomal spastic paraplegia type 30", "hereditary spastic paraplegia type 30", "autosomal dominant spastic paraplegia 30", "SPASTIC PARAPLEGIA 30, AUTOSOMAL DOMINANT", "spastic paraplegia 30, autosomal dominant", "autosomal recessive spastic paraplegia 30", "SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE", "Spastic Paraplegia 30, Autosomal Recessive", "spastic paraplegia 30, autosomal recessive", "Autosomal spastic paraplegia type 30 (disorder)", "hereditary spastic paraplegia caused by mutation in KIF1A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 30", "shortest_name_length": 5}
{"curie": "MONDO:0016854", "names": ["XXXYY syndrome", "49,XXXYY syndrome", "49, XXXYY syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "49,XXXYY syndrome", "shortest_name_length": 14}
{"curie": "UMLS:C4521818", "names": ["0", "Stage 0 Hilar Cholangiocarcinoma", "Stage 0 Hilar Cholangiocarcinoma AJCC v8", "Stage 0 Perihilar Cholangiocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage 0 Hilar Cholangiocarcinoma AJCC v8", "shortest_name_length": 1}
{"curie": "MONDO:0001741", "names": ["hyperpth", "hyperparathyroidism", "Hyperparathyroidism", "HYPERPARATHYROIDISM", "Hyperparathyroidism NOS", "Hyperparathyroidism, NOS", "hyperfunction; parathyroid", "parathyroid; hyperfunction", "PARATHYROID, HYPERFUNCTION", "HPTH - Hyperparathyroidism", "Hyperparathyroidism (disorder)", "hyperparathyroidism (diagnosis)", "Hyperparathyroidism, unspecified", "Elevated blood parathyroid hormone level"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperparathyroidism", "shortest_name_length": 8}
{"curie": "UMLS:C0861876", "names": ["Relapsed Hepatoma", "Hepatoma recurrent", "Recurrent Hepatoma", "Liver carcinoma recurrent", "Carcinoma liver recurrent", "Malignant hepatoma recurrent", "Relapsed Liver Cell Carcinoma", "Liver cell carcinoma recurrent", "Recurrent Liver Cell Carcinoma", "Recurrent Hepatocellular Cancer", "Relapsed Carcinoma of Liver Cell", "Relapsed Hepatocellular Carcinoma", "Recurrent Carcinoma of Liver Cell", "Hepatocellular carcinoma recurrent", "Recurrent Hepatocellular Carcinoma", "Hepatocellular Carcinoma, Recurrent", "Relapsed Carcinoma of the Liver Cell", "Recurrent Carcinoma of the Liver Cell"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Hepatocellular Carcinoma", "shortest_name_length": 17}
{"curie": "UMLS:C4725631", "names": ["Recurrent T-Cell Prolymphocytic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent T-Cell Prolymphocytic Leukemia", "shortest_name_length": 40}
{"curie": "UMLS:C1112211", "names": ["liver infection", "infection liver", "infections liver", "Hepatic infection", "hepatic infection", "Hepatic Infection", "hepatic infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hepatic Infection", "shortest_name_length": 15}
{"curie": "MONDO:0012256", "names": ["SPG28", "hereditary spastic paraplegia 28", "hereditary spastic paraplegia type 28", "autosomal recessive spastic paraplegia 28", "SPASTIC PARAPLEGIA 28, AUTOSOMAL RECESSIVE", "Spastic Paraplegia 28, Autosomal Recessive", "spastic paraplegia 28, autosomal recessive", "autosomal recessive spastic paraplegia type 28", "Autosomal recessive spastic paraplegia type 28", "DDHD1 autosomal recessive pure spastic paraplegia", "SPASTIC PARAPLEGIA 28, AUTOSOMAL RECESSIVE (disorder)", "familial spastic paraplegia autosomal recessive type 28", "Autosomal recessive spastic paraplegia type 28 (disorder)", "Autosomal recessive spastic paraplegia type 28 (diagnosis)", "autosomal recessive pure spastic paraplegia caused by mutation in DDHD1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 28", "shortest_name_length": 5}
{"curie": "MONDO:0012268", "names": ["AIDS", "sida", "aids", "HIV/AIDS", "AIDS, NOS", "HIV / AIDS", "AIDS disorders", "HIV-infection/aids", "hiv-infection/aids", "AIDS HIV infection", "AIDS HIV infections", "HIV-infection (AIDS/ARC)", "Acquired immunodeficiency", "Acquired Immunodeficiency", "Acquired Immune Deficiency", "acquired Immune deficiency", "acquired immune deficiency", "autoimmune deficiency syndrome", "AUTOIMMUNE DEFICIENCY SYNDROME", "Autoimmune deficiency syndrome", "acquired immun-deficiency synd", "Acquired Immun-Deficiency Synd", "ACQUIRED IMMUNE DEFICIENCY SYNDR", "acquired immunodeficiency disease", "Acquired Immunodeficiency Disease", "acquired immunodeficiency syndrome", "Acquired Immunodeficiency Syndrome", "Acquired immunodeficiency syndrome", "Acquired Immuno Deficiency Syndrome", "Syndrome, Acquired Immunodeficiency", "Acquired immune deficiency syndrome", "Acquired Immune Deficiency Syndrome", "Acquired immunodeficiency syndromes", "Acquired Immuno-Deficiency Syndrome", "Acquired immuno deficiency syndrome", "ACQUIRED IMMUNE DEFICIENCY SYNDROME", "acquired immune deficiency syndrome", "acquired; immunodeficiency syndrome", "Acquired Immunodeficiency Syndromes", "Immunodeficiency Syndrome, Acquired", "Immunodeficiency Syndromes, Acquired", "Acquired Immuno-Deficiency Syndromes", "Immuno-Deficiency Syndrome, Acquired", "Syndrome, Acquired Immuno-Deficiency", "Syndromes, Acquired Immunodeficiency", "Syndromes, Acquired Immuno-Deficiency", "Immuno-Deficiency Syndromes, Acquired", "Acquired immunodeficiency syndrome NOS", "Acquired immunodeficiency syndrome, NOS", "IMMUNE DEFICIENCY SYNDROME ACQUIRED AIDS", "AIDS, acquired immunodeficiency syndrome", "Acquired immune deficiency syndrome, NOS", "acquired immunodeficiency syndrome, AIDS", "acquired immunodeficiency syndrome (AIDS)", "AIDS - Acquired immunodeficiency syndrome", "Immunologic Deficiency Syndrome, Acquired", "IMMUNE DEFICIENCY SYNDROME ACQUIRED <AIDS>", "Acquired immune deficiency syndrome (AIDS)", "acquired immune deficiency syndrome [AIDS]", "Acquired immune deficiency syndrome (disorder)", "Acquired immunodeficiency syndrome, unspecified", "acquired immunodeficiency syndrome (HIV-1 stage 6)", "acquired immunodeficiency syndrome (AIDS) (diagnosis)", "Immunodeficiency due to human immunodeficiency virus infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS", "shortest_name_length": 4}
{"curie": "UMLS:C2931135", "names": ["Blepharophimosis syndrome type 1", "Blepharophimosis, ptosis, epicanthus inversus type 1", "Blepharophimosis, ptosis, epicanthus inversus with ovarian failure"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Blepharophimosis syndrome type 1", "shortest_name_length": 32}
{"curie": "UMLS:C0751852", "names": ["polyneuropathy; arsenic", "arsenic; polyneuropathy", "Arsenic Induced Polyneuropathy", "Arsenic-Induced Polyneuropathy", "Polyneuropathy, Arsenic Induced", "Polyneuropathy, Arsenic-Induced", "Arsenic-Induced Polyneuropathies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arsenic Induced Polyneuropathy", "shortest_name_length": 23}
{"curie": "UMLS:C0743301", "names": ["DUODENAL ADENOMA", "Duodenal Adenoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Duodenal Adenoma", "shortest_name_length": 16}
{"curie": "MONDO:0001657", "names": ["brain ca", "ca brain", "Brain Ca", "brain cancer", "Brain Cancer", "Brain Cancers", "Brain--Cancer", "brain cancers", "Cancer, Brain", "Brain Neoplasm", "brain neoplasm", "Cancer of Brain", "cancer of brain", "neoplasm of brain", "BT - brain tumour", "brain tumor adult", "BT - Brain tumour", "Adult Brain Tumor", "adult brain tumor", "adults brain tumor", "tumor of the Brain", "brain tumor, adult", "tumor of the brain", "adult brain tumors", "adults brain tumors", "Cancer of the Brain", "cancer of the brain", "primary brain tumor", "Adult Brain Neoplasm", "Tumor of Adult Brain", "Neoplasm malig;brain", "malignant brain tumor", "brain neoplasm, adult", "Malignant brain tumor", "Malignant Brain Tumor", "BRAIN TUMOR MALIGNANT", "Brain Neoplasms, Adult", "Malignant brain tumour", "malignant brain tumour", "primary brain neoplasm", "brain malignant tumors", "Neoplasm of Adult Brain", "malignant tumor of brain", "BRAIN NEOPLASM MALIGNANT", "Tumor of the Adult Brain", "Brain Malignant Neoplasm", "Malignant Brain Neoplasm", "malignant tumor of Brain", "brain cancer (diagnosis)", "Malignant Tumor of Brain", "Brain neoplasm malignant", "malignant brain neoplasm", "Malignant Brain Neoplasms", "Brain Neoplasm, Malignant", "Brain Malignant Neoplasms", "Malignant Neoplasm, Brain", "brain neoplasms, malignant", "Brain Neoplasms, Malignant", "Malignant Neoplasms, Brain", "Malignant neoplasm of brain", "Neoplasms, Brain, Malignant", "Malignant Adult Brain Tumor", "malignant neoplasm of brain", "Malignant Neoplasm of Brain", "Neoplasm of the Adult Brain", "malignant tumor of the brain", "Malignant brain neoplasm NOS", "Malignant Tumor of the Brain", "malignant primary brain tumor", "Primary Malignant Brain Tumors", "Malignant Primary Brain Tumors", "malignant tumor of adult brain", "Adult Malignant Brain Neoplasm", "Malignant Tumor of Adult Brain", "adult malignant brain neoplasm", "malignant neoplasm of the brain", "Malignant Neoplasm of the Brain", "malignant primary brain neoplasm", "malignant neosplasm of the brain", "brain malignant neoplasm primary", "Malignant neoplasm of brain, NOS", "Malignant Primary Brain Neoplasms", "Primary Malignant Brain Neoplasms", "Brain Neoplasms, Adult, Malignant", "Malignant Tumor of the Adult Brain", "Brain Neoplasms, Primary Malignant", "Primary malignant neoplasm of brain", "primary malignant neoplasm of brain", "Brain Neoplasms, Malignant, Primary", "Brain tumor, adult: General and other", "Malignant neoplasm of brain (disorder)", "malignant neoplasm of brain (diagnosis)", "neoplasm of unspecified nature of brain", "Malignant neoplasm of brain, unspecified", "Primary malignant neoplasm of brain (disorder)", "Primary malignant neoplasm of brain (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brain cancer", "shortest_name_length": 8}
{"curie": "MONDO:0005051", "names": ["Lobular Carcinoma", "carcinoma lobular", "lobular carcinoma", "Lobular carcinoma", "lobular carcinomas", "Carcinoma, Lobular", "Lobular Carcinomas", "Carcinomas, Lobular", "Lobular carcinoma NOS", "Lobular carcinoma, NOS", "Lobular Adenocarcinoma", "Lobular adenocarcinoma", "lobular adenocarcinoma", "lobular breast carcinoma", "Breast Lobular Carcinoma", "lobular carcinoma breast", "breast carcinoma lobular", "Lobular Breast Carcinoma", "invasive lobular carcinoma", "Invasive Lobular Carcinoma", "Invasive lobular carcinoma", "lobular carcinoma of breast", "Lobular Carcinoma of Breast", "Lobular carcinoma of breast", "carcinoma infiltrated lobular", "infiltrating lobular carcinoma", "Infiltrating lobular carcinoma", "invasive lobular adenocarcinoma", "Invasive Lobular Adenocarcinoma", "Lobular Carcinoma of the Breast", "lobular carcinoma of the breast", "Lobular carcinoma of the breast", "Invasive Breast Lobular Carcinoma", "breast invasive lobular carcinoma", "Invasive lobular breast carcinoma", "invasive lobular breast carcinoma", "lobular invasive breast carcinoma", "Invasive Lobular Breast Carcinoma", "Lobular breast carcinoma invasive", "classic invasive lobular carcinoma", "Classic Invasive Lobular Carcinoma", "infiltrating lobular adenocarcinoma", "Infiltrating Lobular Adenocarcinoma", "Invasive Lobular Carcinoma of Breast", "invasive lobular carcinoma of breast", "infiltrating lobular breast carcinoma", "Infiltrating Lobular Breast Carcinoma", "Lobular carcinoma of breast (disorder)", "Invasive pleomorphic lobular carcinoma", "lobular carcinoma of breast (diagnosis)", "Infiltrating lobular carcinoma of breast", "invasive lobular carcinoma, classic type", "Invasive Lobular Carcinoma of the Breast", "infiltrating lobular carcinoma of breast", "Invasive Lobular Carcinoma, Classic Type", "Infiltrating Lobular Carcinoma of Breast", "invasive lobular carcinoma of the breast", "lobular carcinoma (morphologic abnormality)", "Lobular carcinoma (morphologic abnormality)", "infiltrating lobular carcinoma of the breast", "Infiltrating Lobular Carcinoma of the Breast", "lobular carcinoma NOS (morphologic abnormality)", "carcinoma; infiltrating lobular, unspecified site", "infiltrating; lobular carcinoma, unspecified site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "invasive lobular breast carcinoma", "shortest_name_length": 17}
{"curie": "MONDO:0007431", "names": ["DENS IN DENTE AND PALATAL INVAGINATIONS", "dens in dente and palatal invaginations", "Dens in dente and palatal invaginations", "dens in dente and palatal INVAGINATIONS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dens in dente and palatal invaginations", "shortest_name_length": 39}
{"curie": "UMLS:C5554609", "names": ["Recurrent Malignant Nongerminomatous Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Malignant Nongerminomatous Germ Cell Tumor", "shortest_name_length": 52}
{"curie": "UMLS:C4763866", "names": ["Cirrhosis of the Liver Secondary to Hepatitis B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cirrhosis of the Liver Secondary to Hepatitis B", "shortest_name_length": 47}
{"curie": "UMLS:C2010560", "names": ["Hemorrhagic gastritis", "Gastritis hemorrhagic", "GASTRITIS HEMORRHAGIC", "hemorrhagic gastritis", "HEMORRHAGIC GASTRITIS", "Hemorrhagic Gastritis", "Gastritis haemorrhagic", "GASTRITIS HAEMORRHAGIC", "Haemorrhagic gastritis", "Hemorrhagic gastritis (disorder)", "hemorrhagic gastritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemorrhagic gastritis", "shortest_name_length": 21}
{"curie": "OMIM:612267", "names": ["SHEP10", "Skin-Hair-Eye Pigmentation, Variation In, 10", "SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 10", "Skin-Hair-Eye Pigmentation 10, Blond-Brown Hair", "SKIN/HAIR/EYE PIGMENTATION 10, BLOND/BROWN HAIR"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 6}
{"curie": "MONDO:0005649", "names": ["APPENDICITIS", "Appendicitis", "appendicitis", "Appendicitis, NOS", "acute appendicitis", "Acute Appendicitis", "appendix; inflammation", "inflammation; appendix", "Appendicitis (disorder)", "Unqualified appendicitis", "appendicitis (diagnosis)", "Unspecified appendicitis", "Appendicitis, unqualified", "vermiform appendix inflammation", "inflammation of vermiform appendix", "acute appendicitis with peritoneal abscess", "acute appendicitis with generalized peritonitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "appendicitis", "shortest_name_length": 12}
{"curie": "UMLS:C4727402", "names": ["Recurrent Thyroid Gland Follicular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Thyroid Gland Follicular Carcinoma", "shortest_name_length": 44}
{"curie": "UMLS:C4744705", "names": ["Orbital Alveolar Soft Part Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Orbital Alveolar Soft Part Sarcoma", "shortest_name_length": 34}
{"curie": "UMLS:C0346217", "names": ["benign tumor of seminal vesicle", "Benign Seminal Vesicle Neoplasm", "Benign tumor of seminal vesicle", "Benign tumour of seminal vesicle", "benign neoplasm of seminal vesicle", "Benign neoplasm of seminal vesicle", "Benign tumor of seminal vesicle (disorder)", "benign neoplasm of seminal vesicle (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign tumor of seminal vesicle", "shortest_name_length": 31}
{"curie": "MONDO:0000700", "names": ["FHM", "Other migraine", "Mobius' syndrome I", "Other forms of migraine", "Familial hemiplegic migraine", "familial hemiplegic migraine", "Familial Hemiplegic Migraine", "Hemiplegic Migraine, Familial", "hemiplegic migraine, familial", "Familial Hemiplegic Migraines", "hereditary hemiplegic migraine", "hemiplegic-ophthalmoplegic migraine", "Hemiplegic-ophthalmoplegic migraine", "Hemiplegic-Ophthalmoplegic Migraine", "Familial hemiplegic migraine (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial hemiplegic migraine", "shortest_name_length": 3}
{"curie": "MONDO:0010566", "names": ["COD1", "CORDX1", "cone dystrophy X-linked 1", "X-linked cone dystrophy 1", "CONE DYSTROPHY 1, X-LINKED", "cone dystrophy 1, X-linked", "CONE DYSTROPHY, X-LINKED, 1", "Cone Dystrophy, X-Linked, 1", "X-linked cone-rod dystrophy 1", "cone-rod dystrophy X-linked 1", "cone-rod dystrophy, X-linked, 1", "CONE-ROD DYSTROPHY, X-LINKED, 1", "X-linked cone-rod dystrophy type 1", "Cone-Rod Dystrophy, X-Linked, Type 1", "cone-rod dystrophy, X-linked, type 1", "cone-rod dystrophy, X-linked, 1, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked cone-rod dystrophy 1", "shortest_name_length": 4}
{"curie": "UMLS:C1511302", "names": ["Breast Carcinoma with Choriocarcinomatous Features"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Breast Carcinoma with Choriocarcinomatous Features", "shortest_name_length": 50}
{"curie": "MONDO:0015604", "names": ["middle ear anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "middle ear anomaly", "shortest_name_length": 18}
{"curie": "MONDO:0001286", "names": ["Exotropia", "exotropia", "EXOTROPIA", "XT - Exotropia", "Exotropia, NOS", "divergent squint", "Divergent squint", "External strabismus", "Divergent strabismus", "Exotropia (disorder)", "Divergent Strabismus", "divergent strabismus", "STRABISMUS DIVERGENT", "divergent; strabismus", "exotropia (diagnosis)", "strabismus; divergent", "Strabismus, Divergent", "Unspecified exotropia", "Exotropia, unspecified", "Outward facing eye ball", "divergent concomitant strabismus", "Divergent concomitant strabismus", "strabismus; concomitant, divergent", "concomitant; strabismus, divergent", "Divergent concomitant strabismus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exotropia", "shortest_name_length": 9}
{"curie": "MONDO:0010097", "names": ["Tatsumi factor deficiency", "Tatsumi Factor Deficiency", "TATSUMI FACTOR DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tatsumi factor deficiency", "shortest_name_length": 25}
{"curie": "MONDO:0024965", "names": ["Animal Muscular Dystrophy", "animal muscular dystrophy", "Muscular Dystrophy, Animal", "Dystrophy, Animal Muscular", "dystrophy, animal muscular", "Animal Muscular Dystrophies", "animal muscular dystrophies", "Muscular Dystrophies, Animal", "Dystrophies, Animal Muscular", "dystrophies, animal muscular", "muscular dystrophies, animal", "muscular dystrophy, non-human animal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "muscular dystrophy, non-human animal", "shortest_name_length": 25}
{"curie": "MONDO:0017382", "names": ["familial clubfoot due to 5q31 microdeletion", "hereditary clubfoot due to 5q31 microdeletion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial clubfoot due to 5q31 microdeletion", "shortest_name_length": 43}
{"curie": "UMLS:C5207005", "names": ["Cervical Cancer by FIGO Stage 2018", "Cervical Carcinoma by FIGO Stage 2018"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Cancer by FIGO Stage 2018", "shortest_name_length": 34}
{"curie": "UMLS:C0853277", "names": ["Pseudo-Bartter syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pseudo-Bartter syndrome", "shortest_name_length": 23}
{"curie": "UMLS:C5554991", "names": ["Triple-Class Refractory Multiple Myeloma", "Triple-Class Refractory Plasma Cell Myeloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Triple-Class Refractory Plasma Cell Myeloma", "shortest_name_length": 40}
{"curie": "UMLS:C5238930", "names": ["Severe Gastrointestinal Tract Acute Graft Versus Host Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Severe Gastrointestinal Tract Acute Graft Versus Host Disease", "shortest_name_length": 61}
{"curie": "UMLS:C5238359", "names": ["Locally Advanced Fallopian Tube Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Fallopian Tube Carcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0004547", "names": ["reticular pattern testicular yolk sac tumor", "testicular yolk Sac tumor, reticular pattern", "Testicular Yolk Sac Tumor, Reticular Pattern", "testicular yolk Sac tumor, microcystic pattern", "Testicular Yolk Sac Tumor, Microcystic Pattern"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "reticular pattern testicular yolk sac tumor", "shortest_name_length": 43}
{"curie": "MONDO:0024885", "names": ["Malignant Ovarian Serous Tumor", "malignant ovarian serous tumor", "ovarian serous tumor, malignant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant ovarian serous tumor", "shortest_name_length": 30}
{"curie": "UMLS:C0235551", "names": ["Edema laryngotracheal", "EDEMA LARYNGOTRACHEAL", "LARYNGOTRACHEAL EDEMA", "Laryngotracheal edema", "Laryngotracheal oedema", "LARYNGOTRACHEAL OEDEMA", "Oedema laryngotracheal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Laryngotracheal edema", "shortest_name_length": 21}
{"curie": "MONDO:0002799", "names": ["nodular medulloblastoma", "desmoplastic/nodular medulloblastoma", "desmoplastic nodular medulloblastoma", "Medulloblastoma with extensive nodularity", "Medulloblastoma SHH-Activated TP53-Wildtype", "Medulloblastoma, SHH-Activated, TP53-Wildtype", "Medulloblastoma, SHH-activated and TP53-wildtype", "medulloblastoma SHH activated and TP53 wild-type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nodular medulloblastoma", "shortest_name_length": 23}
{"curie": "MONDO:0060779", "names": ["Acquired Fanconi syndrome", "Acquired Fanconi Syndrome", "Fanconi syndrome acquired", "acquired Fanconi syndrome", "Secondary Fanconi syndrome", "Acquired Fanconi syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired Fanconi syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0011903", "names": ["CMT2J", "Cmt2j", "CMT 2J", "Charcot-Marie-Tooth disease type 2J", "Charcot Marie Tooth disease type 2J", "Charcot-Marie-Tooth disease, Type 2J", "CHARCOT-MARIE-TOOTH DISEASE, TYPE 2J", "Charcot-Marie-Tooth disease, type 2J", "Charcot-Marie-Tooth neuropathy type 2J", "CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2J", "Charcot-Marie-Tooth neuropathy, type 2J", "Charcot-Marie-Tooth Neuropathy, Type 2j", "Charcot-Marie-Tooth disease, axonal, type 2J", "Charcot-Marie-Tooth disease, axonal, Type 2J", "CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2J", "Charcot-Marie-Tooth disease type 2J (diagnosis)", "Autosomal dominant Charcot-Marie-Tooth disease type 2J", "autosomal dominant Charcot-Marie-Tooth disease type 2J", "Autosomal dominant Charcot-Marie-Tooth disease type 2J (disorder)", "Charcot-Marie-Tooth disease type 2 with hearing loss and pupillary abnormalities", "Charcot-Marie-Tooth disease, Type 2, with hearing loss and pupillary abnormalities", "CHARCOT-MARIE-TOOTH DISEASE, TYPE 2, WITH HEARING LOSS AND PUPILLARY ABNORMALITIES", "Charcot-Marie-Tooth disease, type 2, with hearing loss and pupillary abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Charcot-Marie-Tooth disease type 2J", "shortest_name_length": 5}
{"curie": "MONDO:0017361", "names": ["CRS", "Gregg's syndrome", "rubella congenital", "Congenital rubella", "congenital rubella", "Congenital Rubella", "Rubella;congenital", "congenital; rubella", "rubella; congenital", "fetal rubella syndrome", "Fetal rubella syndrome", "Congenital Rubella Syndrome", "rubella congenital syndrome", "Congenital rubella syndrome", "RUBELLA CONGENITAL SYNDROME", "syndrome rubella congenital", "congenital rubella syndrome", "Syndrome, Congenital Rubella", "Rubella syndrome, congenital", "Gestational rubella syndrome", "Rubella Syndrome, Congenital", "Congenital Rubella Syndromes", "Rubella Syndromes, Congenital", "Rubella syndrome, gestational", "Syndromes, Congenital Rubella", "syndrome; congenital rubella, manifest", "Congenital rubella syndrome (disorder)", "syndrome; rubella, manifest, congenital", "congenital rubella syndrome (diagnosis)", "Mother-to-child transmission of rubella syndrome", "mother-to-child transmission of rubella syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital rubella syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0014932", "names": ["OFD15", "Ofds 15", "OFDS XV", "OROFACIODIGITAL SYNDROME XV", "orofaciodigital syndrome 15", "orofaciodigital syndrome XV", "orofaciodigital syndrome type XV", "oral-Facial-digital syndrome, type 15", "ORAL-FACIAL-DIGITAL SYNDROME, TYPE XV"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orofaciodigital syndrome XV", "shortest_name_length": 5}
{"curie": "MONDO:0030768", "names": ["JEB5A", "EPIDERMOLYSIS BULLOSA, JUNCTIONAL 5A, INTERMEDIATE", "epidermolysis bullosa, junctional 5A, intermediate", "epidermolysis bullosa, junctional 5A, non-herlitz IIA", "EPIDERMOLYSIS BULLOSA, JUNCTIONAL 5A, NON-HERLITZ TYPE", "EPIDERMOLYSIS BULLOSA, JUNCTIONAL 5A, GENERALIZED INTERMEDIATE", "epidermolysis bullosa, junctional 5A, generalized intermediate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "epidermolysis bullosa, junctional 5A, intermediate", "shortest_name_length": 5}
{"curie": "UMLS:C0854777", "names": ["recurrent pancreas cancer", "pancreas cancer, recurrent", "Relapsed Pancreatic Cancer", "Pancreatic cancer recurrent", "Recurrent Pancreatic Cancer", "Relapsed Cancer of Pancreas", "recurrent pancreatic cancer", "pancreatic cancer, recurrent", "Recurrent Cancer of Pancreas", "Pancreas carcinoma recurrent", "Relapsed Pancreatic Carcinoma", "Relapsed Carcinoma of Pancreas", "Recurrent Pancreatic Carcinoma", "Pancreatic carcinoma recurrent", "Pancreatic Carcinoma, Recurrent", "Recurrent Carcinoma of Pancreas", "Relapsed Cancer of the Pancreas", "Recurrent Cancer of the Pancreas", "Relapsed Carcinoma of the Pancreas", "Recurrent Carcinoma of the Pancreas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic carcinoma recurrent", "shortest_name_length": 25}
{"curie": "UMLS:C1262091", "names": ["infiltration lymphocytic", "lymphocytic infiltration", "Lymphocytic infiltration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lymphocytic infiltration", "shortest_name_length": 24}
{"curie": "UMLS:C0279550", "names": ["Rhabdomyosarcoma", "Adult Rhabdomyosarcoma", "adult rhabdomyosarcoma", "sarcoma, adult rhabdo-", "rhabdomyosarcoma, adult"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Rhabdomyosarcoma", "shortest_name_length": 16}
{"curie": "MONDO:0019626", "names": ["isolated ankyloblepharon filiforme adnatum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated ankyloblepharon filiforme adnatum", "shortest_name_length": 42}
{"curie": "MONDO:0019204", "names": ["RB-ILD", "respiratory bronchiolitis-interstitial lung disease syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "respiratory bronchiolitis-interstitial lung disease syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0003617", "names": ["Salpingitis;chronic", "Chronic salpingitis", "chronic salpingitis", "Chronic Salpingitis", "salpingitis; chronic", "salpingitis, chronic", "chronic; salpingitis", "SALPINGITIS, CHRONIC", "Salpingitis chronic NOS", "Chronic salpingitis (disorder)", "chronic salpingitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic salpingitis", "shortest_name_length": 19}
{"curie": "UMLS:C1336230", "names": ["Stage IIIB Small Cell Lung Cancer", "Stage IIIB Small Cell Lung Carcinoma", "Stage IIIB Small Cell Carcinoma of Lung", "Stage IIIB Small Cell Carcinoma of the Lung", "Stage IIIB Lung Small Cell Carcinoma AJCC v7", "Stage IIIB Small Cell Lung Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIB Lung Small Cell Carcinoma AJCC v7", "shortest_name_length": 33}
{"curie": "MONDO:0008872", "names": ["Mopd2", "MOPD2", "Mopd 2", "MopdII", "MOPD II", "MOPD type II", "dwarfism, MOPD type II", "dwarfism, MOPD type II (diagnosis)", "osteodysplastic primordial dwarfism type 2", "Osteodysplastic Primordial Dwarfism Type Ii", "Osteodysplastic primordial dwarfism, type 2", "osteodysplastic primordial dwarfism type II", "osteodysplastic primordial dwarfism, type 2", "Osteodysplastic Primordial Dwarfism, Type II", "OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II", "Majewski Osteodysplastic Primordial Dwarfism Type II", "Majewski osteodysplastic primordial dwarfism type II", "microcephalic osteodysplastic primordial dwarfism type 2", "Microcephalic Osteodysplastic Primordial Dwarfism Type II", "Microcephalic osteodysplastic primordial dwarfism, type 2", "Microcephalic osteodysplastic primordial dwarfism type II", "microcephalic osteodysplastic primordial dwarfism type II", "microcephalic osteodysplastic primordial dwarfism, type 2", "microcephalic osteodysplastic primordial dwarfism, type II", "Microcephalic Osteodysplastic Primordial Dwarfism, Type II", "MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II", "Microcephalic osteodysplastic primordial dwarfism type II (disorder)", "MOPD type II - microcephalic osteodysplastic primordial dwarfism type II", "microcephalic osteodysplastic primordial dwarfism with tooth abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephalic osteodysplastic primordial dwarfism type II", "shortest_name_length": 5}
{"curie": "UMLS:C2931648", "names": ["Larsen syndrome, dominant type", "Larsen Syndrome, Autosomal Dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Larsen syndrome, dominant type", "shortest_name_length": 30}
{"curie": "MONDO:0100404", "names": ["AML, MLL Rearrangement", "AML, KMT2A Rearrangement", "Acute myeloid leukemia, MLL", "AML, MLL gene rearrangement", "Acute myeloid leukaemia, MLL", "AML with 11q23 abnormalities", "AML, KMT2A Gene Rearrangement", "Acute Myeloid Leukemia with MLLr", "Acute myeloid leukemia, 11q23 abnormalities", "acute myeloid leukemia, 11q23 abnormalities", "Acute myeloid leukaemia, 11q23 abnormalities", "Acute myeloid leukemia with 11q23-abnormality", "Acute Myeloid Leukemia with MLL Rearrangement", "Acute myeloid leukemia with 11q23 abnormality", "acute myeloid leukemia with MLL rearrangement", "acute myeloid leukemia, MLL gene rearrangement", "AML, Mixed Lineage Leukemia Gene Rearrangement", "Acute myeloid leukaemia with 11q23 abnormality", "Acute myeloid leukemia with 11q23 abnormalities", "Acute Myeloid Leukemia with 11q23 Abnormalities", "AML, Myeloid/Lymphoid Leukemia Gene Rearrangement", "Acute myeloid leukemia with 11q23-abnormality NOS", "acute myelogenous leukemia with 11q23 abnormalities", "AML, Lysine Methyltransferase 2A Gene Rearrangement", "Acute Myeloid Leukemia with KMT2A/MLL Rearrangement", "Acute myeloid leukemia with 11q23 abnormality (disorder)", "acute myelogenous leukemia with 11q23 abnormalities (diagnosis)", "AML, Lysine (K)-Specific Methyltransferase 2A Gene Rearrangement", "AML, Myeloid/Lymphoid or Mixed Lineage Leukemia Gene Rearrangement", "Acute myeloid leukemia, 11q23 abnormalities (morphologic abnormality)", "AML, Myeloid/Lymphoid or Mixed-Lineage Leukemia (Trithorax Homolog, Drosophila) Gene Rearrangement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, MLL gene rearrangement", "shortest_name_length": 22}
{"curie": "UMLS:C1336216", "names": ["Stage IIIA Squamous Cell Lung Cancer", "Stage IIIA Squamous Cell Lung Carcinoma", "Stage IIIA Squamous Cell Carcinoma of Lung", "Stage IIIA Squamous Cell Carcinoma of the Lung", "Stage IIIA Squamous Cell Lung Carcinoma AJCC v7", "Stage IIIA Lung Squamous Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Lung Squamous Cell Carcinoma AJCC v7", "shortest_name_length": 36}
{"curie": "MONDO:0008723", "names": ["VLCAD", "Acadvl", "VLCADD", "Vlcad-H", "Vlcad-C", "ACADVLD", "VLCAD DEFICIENCY", "VLCAD deficiency", "Very Long-Chain Acyl-CoA Dehydrogenase Deficiency", "Acyl-Coa Dehydrogenase Very Long Chain Deficiency", "Very long-chain acyl-CoA dehydrogenase deficiency", "Very long chain acyl-CoA dehydrogenase deficiency", "very long chain acyl-CoA dehydrogenase deficiency", "very long-chain acyl-CoA dehydrogenase deficiency", "Acyl-CoA Dehydrogenase, Very Long-Chain Deficiency", "acyl-CoA dehydrogenase, very long-chain deficiency", "acyl-CoA dehydrogenase, very long-chain, deficiency OF", "ACYL-CoA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF", "Acyl-CoA Dehydrogenase, Very Long-Chain, Deficiency of", "Very long chain acyl-coenzyme A dehydrogenase deficiency", "Very long-chain acyl-coenzyme A dehydrogenase deficiency", "Very Long-Chain Acyl-Coenzyme A Dehydrogenase Deficiency", "very long-chain acyl-Coenzyme A dehydrogenase deficiency", "Very Long-Chain Acyl Coenzyme A Dehydrogenase Deficiency", "VLCAD - Very long chain acyl-CoA dehydrogenase deficiency", "very long chain acyl-CoA dehydrogenase deficiency (diagnosis)", "Very long chain acyl-coenzyme A dehydrogenase deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "very long chain acyl-CoA dehydrogenase deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C4524735", "names": ["Pathologic Stage III Gastroesophageal Junction Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage III Gastroesophageal Junction Adenocarcinoma AJCC v8", "shortest_name_length": 69}
{"curie": "MONDO:0008207", "names": ["PATELLA, CHONDROPATHY", "chondropathy; patella", "patella; chondropathy", "chondropathia patellae", "PATELLA CHONDROMALACIA", "chondromalacia patella", "patella chondromalacia", "Chondromalacia patella", "CHONDROPATHIA PATELLAE", "Chondromalacia;patella", "chondromalacia; patella", "patellar chondromalacia", "Chondromalacia Patellae", "patella; chondromalacia", "PATELLA, CHONDROMALACIA", "CHONDROMALACIA PATELLAE", "patellae chondromalacia", "Chondromalacia patellae", "chondromalacia patellae", "chondromalacia of patella", "Chondromalacia of patella", "Patella, Chondromalacia Of", "PATELLA, CHONDROMALACIA OF", "patella, chondromalacia OF", "familial chondromalacia patellae", "Buedinger-Ludloff-Laewen disease", "Chondromalacia patellae syndrome", "patellar chondromalacia (diagnosis)", "Chondromalacia of patella (disorder)", "Softening of articular cartilage of patella", "softening of articular cartilage of patella", "Degeneration of articular cartilage of patella"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chondromalacia patellae", "shortest_name_length": 21}
{"curie": "UMLS:C0235831", "names": ["Renal Dysplasia", "RENAL DYSPLASIA", "Renal Cell Dysplasia", "Renal cell dysplasia", "CELL DYSPLASIA KIDNEY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Renal Cell Dysplasia", "shortest_name_length": 15}
{"curie": "UMLS:C0751668", "names": ["SCA3, Joseph type", "Type I Machado-Joseph Disease", "Machado-Joseph disease type 1", "Machado Joseph Disease Type I", "Machado-Joseph Disease Type I", "Type I Machado Joseph Disease", "Spinocerebellar ataxia type 3, Joseph type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Machado-Joseph Disease Type I", "shortest_name_length": 17}
{"curie": "MONDO:0020298", "names": ["UPD(15)mat", "Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15", "Prader-Willi syndrome due to maternal uniparental disomy of chromosome type 15"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15", "shortest_name_length": 10}
{"curie": "UMLS:C3662038", "names": ["Chronic kidney disease due to type 2 diabetes mellitus", "Chronic renal impairment due to type 2 diabetes mellitus", "Chronic renal impairment due to type II diabetes mellitus", "Diabetic chronic renal impairment due to type 2 diabetes mellitus", "Chronic kidney disease due to type 2 diabetes mellitus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic kidney disease due to type 2 diabetes mellitus", "shortest_name_length": 54}
{"curie": "MONDO:0033311", "names": ["JBTS33", "Joubert syndrome 33", "JOUBERT SYNDROME 33"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Joubert syndrome 33", "shortest_name_length": 6}
{"curie": "UMLS:C0433991", "names": ["injury inner ear", "inner ear injury", "Injury of inner ear", "injury of inner ear", "Injury of Inner Ear", "Injury of inner ear (disorder)", "Injury of inner ear (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury of inner ear", "shortest_name_length": 16}
{"curie": "MONDO:0100428", "names": ["Fazio-Londe", "Fazio-Londe disease", "Fazio-Londe Disease", "FAZIO-LONDE DISEASE", "Fazio Londe Disease", "Disease, Fazio-Londe", "Fazio Londe Syndrome", "Fazio-Londe Syndrome", "Fazio-Londe syndrome", "Fazio-Londe's disease", "Fazio-Londe's Disease", "Syndrome, Fazio-Londe", "Fazio Londe's Disease", "Fazio-Londe's Syndrome", "Fazio Londe's Syndrome", "Disease, Fazio-Londe's", "Syndrome, Fazio-Londe's", "Childhood Progressive Bulbar Palsy", "progressive bulbar palsy of childhood", "Progressive Bulbar Palsy of Childhood", "Progressive bulbar palsy of childhood", "BULBAR PALSY, PROGRESSIVE, OF CHILDHOOD", "Bulbar Palsy, Progressive, Of Childhood", "riboflavin transporter deficiency neuronopathy", "Progressive bulbar palsy of childhood (disorder)", "Progressive bulbar palsy of childhood [Fazio-Londe]"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive bulbar palsy of childhood", "shortest_name_length": 11}
{"curie": "UMLS:C4744487", "names": ["Refractory Visual Pathway Glioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Visual Pathway Glioma", "shortest_name_length": 32}
{"curie": "MONDO:0008412", "names": ["Katayama fever", "BILHARZIASIS, INTESTINE", "schistosomiasis japonica", "intestinal schistosomiasis", "Intestinal schistosomiasis", "Intestinal Schistosomiases", "Intestinal Schistosomiasis", "Schistosomiases, Intestinal", "schistosomiasis; intestinal", "Schistosomiasis, Intestinal", "intestinal; schistosomiasis", "Intestinal schistosomiasis NOS", "Schistosoma japonicum infection", "Intestinal schistosomiasis (disorder)", "Schistosoma mansoni infectious disease", "Schistosoma mansoni, intensity of infection by", "Schistosoma mansoni infection, susceptibility/resistance to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intestinal schistosomiasis", "shortest_name_length": 14}
{"curie": "MONDO:0010215", "names": ["XPF", "XP6", "XP-F", "XPF/CS", "XP group F", "XP, group F", "XP, Group F", "XP, GROUP F", "xeroderma pigmentosum 6", "xeroderma pigmentosum VI", "XERODERMA PIGMENTOSUM VI", "Xeroderma Pigmentosum Vi", "ERCC4 xeroderma pigmentosum", "xeroderma pigmentosum group F", "Xeroderma pigmentosum group F", "xeroderma pigmentosum, type 6", "Xeroderma Pigmentosum Group F", "Xeroderma pigmentosum, group F", "xeroderma pigmentosum, group F", "xeroderma pigmentosum group type F", "Xeroderma pigmentosum, group F (disorder)", "xeroderma pigmentosum, complementation group F", "Xeroderma Pigmentosum, Complementation Group F", "XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP F", "xeroderma pigmentosum, type F/Cockayne syndrome", "XERODERMA PIGMENTOSUM, TYPE F/COCKAYNE SYNDROME", "xeroderma pigmentosum caused by mutation in ERCC4", "xeroderma pigmentosum, complementation group type F"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "xeroderma pigmentosum group F", "shortest_name_length": 3}
{"curie": "UMLS:C0023439", "names": ["Acute Eosinophilic Leukemia", "acute leukemia eosinophilic", "Acute eosinophilic leukemia", "Acute Eosinophilic Leukemias", "Acute eosinophilic leukaemia", "Eosinophilic Leukemia, Acute", "Leukemia, Acute Eosinophilic", "Eosinophilic Leukemias, Acute", "Leukemia, Eosinophilic, Acute", "Leukemias, Acute Eosinophilic", "Acute eosinophilic leukemia (disorder)", "Acute eosinophilic leukemia (diagnosis)", "Acute eosinophilic leukemia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leukemia, Eosinophilic, Acute", "shortest_name_length": 27}
{"curie": "UMLS:C0341583", "names": ["Esophageal Anastomotic Stricture", "Esophageal anastomotic stricture", "Oesophageal anastomotic stricture", "Esophageal anastomotic stricture (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal anastomotic stricture", "shortest_name_length": 32}
{"curie": "UMLS:C5555068", "names": ["Central Atypical Cartilaginous Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Atypical Cartilaginous Tumor", "shortest_name_length": 36}
{"curie": "MONDO:0006470", "names": ["tonsil scc", "Tonsil SCC", "tonsillar scc", "Tonsillar SCC", "scc of tonsil", "SCC of Tonsil", "SCC of the Tonsil", "scc of the tonsil", "Tonsil Squamous Cell Carcinoma", "squamous cell carcinoma of tonsil", "Tonsillar Squamous Cell Carcinoma", "Squamous cell carcinoma of tonsil", "tonsillar squamous cell carcinoma", "Squamous Cell Carcinoma of Tonsil", "squamous cell carcinoma of the tonsil", "Squamous Cell Carcinoma of the Tonsil", "palatine tonsil squamous cell carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tonsillar squamous cell carcinoma", "shortest_name_length": 10}
{"curie": "MONDO:0009538", "names": ["lymphoid system deterioration, progressive", "LYMPHOID SYSTEM DETERIORATION, PROGRESSIVE", "Lymphoid System Deterioration, Progressive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphoid system deterioration, progressive", "shortest_name_length": 42}
{"curie": "MONDO:0008205", "names": ["PTLAH", "Absent patella", "absent patella", "Absent/small kneecap", "Small to absent patellae", "Absent/hypoplastic patella", "Patella aplasia/hypoplasia", "Patella aplasia-hypoplasia", "patella aplasia-hypoplasia", "patella aplasia/hypoplasia", "PATELLA APLASIA-HYPOPLASIA", "Patellar aplasia/hypoplasia", "patella aplasia or hypoplasia", "Hypoplastic or absent patella", "Absent/underdeveloped kneecap", "Absent or hypoplastic patellae", "familial absence of the patella", "Aplastic or hypoplastic patellae", "Aplasia/Hypoplasia of the patella", "familial aplasia of the patella (subtype)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "patella aplasia/hypoplasia", "shortest_name_length": 5}
{"curie": "UMLS:C1698193", "names": ["Urostomy leak", "Urostomy Leakage", "Urostomy leak (diagnosis)", "postprocedural complications urostomy leak"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Urostomy Leakage", "shortest_name_length": 13}
{"curie": "UMLS:C5446866", "names": ["Recurrent Epithelioid Mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Epithelioid Mesothelioma", "shortest_name_length": 34}
{"curie": "MONDO:0011427", "names": ["ASCARIASIS, SUSCEPTIBILITY TO", "ascariasis, susceptibility to", "ASCARIS LUMBRICOIDES INFECTION, SUSCEPTIBILITY TO", "Ascaris lumbricoides infection, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ascaris lumbricoides infection, susceptibility to", "shortest_name_length": 29}
{"curie": "UMLS:C0270458", "names": ["Psychotic depression", "Psychotic depression, NOS", "Severe major depression with psychotic features", "major depression severe with psychotic features", "Severe major depression with psychotic features, NOS", "severe major depressive disorder with psychotic features", "Severe major depression with psychotic features (disorder)", "severe major depressive disorder with psychotic features (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Severe major depression with psychotic features", "shortest_name_length": 20}
{"curie": "UMLS:C0269125", "names": ["first degree uterine prolapse", "First degree uterine prolapse", "First Degree Uterine Prolapse", "uterus; prolapse, first degree", "Uterine prolapse, first degree", "prolapse; uterus, first degree", "First degree uterine prolapse (disorder)", "first degree uterine prolapse (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "First degree uterine prolapse", "shortest_name_length": 29}
{"curie": "UMLS:C1336246", "names": ["stage III extragonadal seminoma", "Stage III Extragonadal Seminoma", "Stage III Extragonadal Primary Seminoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Extragonadal Seminoma", "shortest_name_length": 31}
{"curie": "MONDO:0030885", "names": ["ALS26", "AMYOTROPHIC LATERAL SCLEROSIS 26 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA", "amyotrophic lateral sclerosis 26 with or without frontotemporal dementia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyotrophic lateral sclerosis 26 with or without frontotemporal dementia", "shortest_name_length": 5}
{"curie": "MONDO:0005079", "names": ["polyp", "POLYP", "Polyp", "POLYPS", "polyps", "Polyps", "Polyp(s)", "Polyp NOS", "Polyp, NOS", "Polyp (disorder)", "Polyp (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyp", "shortest_name_length": 5}
{"curie": "MONDO:0010174", "names": ["Valinemia", "VALINEMIA", "valinemia", "Valinaemia", "hypervalinemia", "Hypervalinemia", "HYPERVALINEMIA", "Hypervalinaemia", "hypervalinemia; disorder", "disorder; hypervalinemia", "Hypervalinemia (disorder)", "hypervalinemia (diagnosis)", "Valine transaminase deficiency", "valine transaminase deficiency", "VALINE TRANSAMINASE DEFICIENCY", "High blood valine concentration"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Valinemia", "shortest_name_length": 9}
{"curie": "MONDO:0000688", "names": ["organic aciduria", "organic acidemia", "inborn organic aciduria", "inherited organic acidemia", "Organic acid metabolism disorder", "Organic Acid Metabolism Disorder", "organic acid metabolism disorder", "disorder of organic acid metabolism", "Disorder of Organic Acid Metabolism", "Disorder of organic acid metabolism", "inborn organic acid metabolic process disorder", "inborn error of organic acid metabolic process", "Disorder of organic acid metabolism (disorder)", "rare inborn error of organic acid metabolic process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn organic aciduria", "shortest_name_length": 16}
{"curie": "MONDO:0000270", "names": ["Lower respiratory disease", "Lower respiratory disorder", "respiratory disorders lower", "lower respiratory tract disease", "lower respiratory tract disorder", "disease of lower respiratory tract", "disorder of lower respiratory tract", "Disorder of lower respiratory system", "Other disease of nasal cavity and sinuses", "Other diseases of nasal cavity and sinuses", "lower respiratory tract disease or disorder", "disease or disorder of lower respiratory tract", "Disorder of lower respiratory system (disorder)", "Disorder of lower respiratory system (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lower respiratory tract disorder", "shortest_name_length": 25}
{"curie": "MONDO:0030692", "names": ["IMD95", "IMMUNODEFICIENCY 95", "immunodeficiency 95"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 95", "shortest_name_length": 5}
{"curie": "UMLS:C5556697", "names": ["Recurrent Medulloblastoma, WNT-Activated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Medulloblastoma, WNT-Activated", "shortest_name_length": 40}
{"curie": "MONDO:0016024", "names": ["shoulder and thorax deformity-congenital heart disease syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "shoulder and thorax deformity-congenital heart disease syndrome", "shortest_name_length": 63}
{"curie": "MONDO:0013997", "names": ["FFDD4", "Type 4 FFDD", "Type 4 FFDDs", "FFDD, Type 4", "FFDD type IV", "focal facial dermal dysplasia 4", "FOCAL FACIAL DERMAL DYSPLASIA 4", "Focal Facial Dermal Dysplasia 4", "Focal facial dermal dysplasia 4", "focal facial preauricular dysplasia", "Focal facial preauricular dysplasia", "focal Facial dermal dysplasia type 4", "Focal Facial Dermal Dysplasia Type 4", "focal facial dermal dysplasia type IV", "Focal facial dermal dysplasia type IV", "Focal facial dermal dysplasia type IV (disorder)", "FFDD type 4 - focal facial dermal dysplasia type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal facial dermal dysplasia type IV", "shortest_name_length": 5}
{"curie": "MONDO:0024415", "names": ["Acute duodenitis", "Erosive duodenitis", "erosive duodenitis", "hemorrhagic duodenitis", "Duodenitis hemorrhagic", "Hemorrhagic duodenitis", "DUODENITIS HEMORRHAGIC", "Haemorrhagic duodenitis", "Duodenitis haemorrhagic", "Duodenitis with bleeding", "duodenitis with bleeding", "multiple duodenal erosions", "Multiple duodenal erosions", "Acute duodenitis (disorder)", "Duodenitis, with hemorrhage", "Duodenitis, with haemorrhage", "Hemorrhagic duodenitis (disorder)", "duodenitis with bleeding (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemorrhagic duodenitis", "shortest_name_length": 16}
{"curie": "UMLS:C0006848", "names": ["Mucocutaneous Candidiasis", "mucocutaneous candidiasis", "Mucocutaneous candidiasis", "Candidiasis, mucocutaneous", "Mucocutaneous candidiasis (disorder)", "mucocutaneous candidiasis (diagnosis)", "Candida infection of skin and mucous membranes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mucocutaneous candidiasis", "shortest_name_length": 25}
{"curie": "MONDO:0006209", "names": ["fibrous tumor", "Fibrous Tumor", "fibrogenicTumor", "FibrogenicTumor", "Fibrocytic Tumor", "Fibrous Neoplasm", "fibrous neoplasm", "fibrocytic tumor", "fibroblastic tumor", "Fibroblastic Tumor", "Fibrocytic Neoplasm", "Fibrogenic Neoplasm", "fibrogenic neoplasm", "fibrocytic neoplasm", "Fibroblastic Neoplasm", "fibroblastic neoplasm", "Fibrous Tissue Neoplasm", "Fibrous tissue neoplasm", "Fibrous Tissue Neoplasms", "Neoplasm, Fibrous Tissue", "Neoplasms, Fibrous Tissue", "neoplasm of fibrous tissue", "neoplasm of fibrous tissue (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibroblastic neoplasm", "shortest_name_length": 13}
{"curie": "UMLS:C0854097", "names": ["Hypoesthesia eye", "Hypoaesthesia eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hypoesthesia eye", "shortest_name_length": 16}
{"curie": "UMLS:C4331997", "names": ["Stage IVC Unknown Primary Tumor (Except for EBV-Related and HPV-Related Tumors) and Metastatic Cervical Adenopathy AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Unknown Primary Tumor (Except for EBV-Related and HPV-Related Tumors) and Metastatic Cervical Adenopathy AJCC v8", "shortest_name_length": 122}
{"curie": "MONDO:0012610", "names": ["IBD10", "inflammatory bowel disease 10", "Inflammatory Bowel Disease 10", "inflammatory bowel disease type 10", "ATG16L1 inflammatory bowel disease", "INFLAMMATORY BOWEL DISEASE (CROHN DISEASE) 10", "inflammatory bowel disease (Crohn disease) 10", "inflammatory bowel disease caused by mutation in ATG16L1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory bowel disease 10", "shortest_name_length": 5}
{"curie": "MONDO:0006246", "names": ["high grade surface osteosarcoma", "High Grade Surface Osteosarcoma", "high-grade surface osteosarcoma", "High grade surface osteosarcoma", "High-Grade Surface Osteosarcoma", "High grade surface osteosarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "high grade surface osteosarcoma", "shortest_name_length": 31}
{"curie": "UMLS:C3544166", "names": ["Alveolar lung disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Alveolar lung disease", "shortest_name_length": 21}
{"curie": "MONDO:0014708", "names": ["Ring 14", "Ring 14 Syndrome", "Ring 14 syndrome", "Chromosome 14 ring", "ring chromosome 14", "chromosome 14 ring", "Ring Chromosome 14", "Ring chromosome 14", "Ring chromosome type 14", "RING chromosome 14 syndrome", "Ring Chromosome 14 Syndrome", "RING CHROMOSOME 14 SYNDROME", "Ring chromosome 14 syndrome", "Ring chromosome 14 syndrome (disorder)", "ring chromosome 14 syndrome, isolated cases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ring chromosome 14", "shortest_name_length": 7}
{"curie": "UMLS:C1879809", "names": ["Teratoid medulloepithelioma, benign", "Benign Intraocular Teratoid Medulloepithelioma", "Ciliary Body Benign Teratoid Medulloepithelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ciliary Body Benign Teratoid Medulloepithelioma", "shortest_name_length": 35}
{"curie": "MONDO:0019434", "names": ["SJIA", "sJIA", "sJRA", "SoJIA", "Systemic JRA", "STILL DISEASE", "disease still", "Still disease", "still disease", "Still Disease", "disease stills", "STILL'S DISEASE", "Still's disease", "Still's Disease", "disease still's", "still's disease", "systemic-onset JIA", "SYSTEMIC ONSET JRA", "Systemic-onset JIA", "systemic onset jra", "Still's disease NOS", "systemic polyarthritis", "juvenile Still's disease", "Chauffard-Still's disease", "Still's disease (formerly)", "Juvenile RA, Systemic Onset", "Juvenile Systemic Arthritis", "Juvenile RA, systemic onset", "Juvenile-Onset Still Disease", "Arthritis, Juvenile Systemic", "Systemic Arthritis, Juvenile", "Juvenile Onset Still Disease", "Juvenile Onset Stills Disease", "Still Disease, Juvenile-Onset", "Still Disease, Juvenile Onset", "Juvenile-Onset Stills Disease", "Juvenile-Onset Still's Disease", "juvenile onset Still's disease", "Juvenile onset Still's disease", "Stills Disease, Juvenile-Onset", "Still's Disease, Juvenile-Onset", "Still's Disease, Juvenile Onset", "Juvenile arthritis with systemic onset", "Systemic juvenile idiopathic arthritis", "Systemic Juvenile Rheumatoid Arthritis", "SYSTEMIC JUVENILE RHEUMATOID ARTHRITIS", "systemic juvenile idiopathic arthritis", "Systemic Juvenile Idiopathic Arthritis", "Rheumatoid Arthritis, Systemic Juvenile", "RHEUMATOID ARTHRITIS, SYSTEMIC JUVENILE", "arthritis; juvenile, with systemic onset", "juvenile; arthritis, with systemic onset", "Systemic onset juvenile chronic arthritis", "juvenile onset Still's disease (diagnosis)", "Systemic Juvenile Rheumatoid Arthritis (AQ)", "Systemic onset juvenile idiopathic arthritis", "Systemic-onset juvenile idiopathic arthritis", "systemic onset juvenile rheumatoid arthritis", "systemic onset juvenile idiopathic arthritis", "Systemic Onset Juvenile Rheumatoid Arthritis", "systemic-onset juvenile idiopathic arthritis", "Systemic Onset Juvenile Idiopathic Arthritis", "Systemic onset juvenile rheumatoid arthritis", "Juvenile rheumatoid arthritis with systemic onset", "Systemic onset juvenile chronic arthritis (disorder)", "Juvenile rheumatoid arthritis with systemic onset, unspecified site"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "systemic-onset juvenile idiopathic arthritis", "shortest_name_length": 4}
{"curie": "MONDO:0006963", "names": ["Sebaceous Tumor", "sebaceous tumor", "sebaceous; tumor", "tumor; sebaceous", "Sebaceous Neoplasm", "Sebaceous neoplasm", "sebaceous neoplasm", "Sebaceous Gland Tumor", "sebaceous gland tumor", "Sebaceous gland tumors", "tumor of sebaceous gland", "sebaceous gland neoplasm", "Sebaceous Gland Neoplasm", "Sebaceous glands--Tumors", "Sebaceous Gland Neoplasms", "Neoplasm, Sebaceous Gland", "Neoplasms, Sebaceous Gland", "neoplasm of sebaceous gland", "Neoplasm of sebaceous gland", "sebaceous gland neoplasm (disease)", "Neoplasm of sebaceous gland (diagnosis)", "Tumor of skin with sebaceous differentiation", "Tumour of skin with sebaceous differentiation", "neoplasm of integumentary system sebaceous gland", "Tumor of skin with sebaceous differentiation (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sebaceous gland neoplasm", "shortest_name_length": 15}
{"curie": "MONDO:0002205", "names": ["melanoma; vulva", "Vulvar Melanoma", "vulvar melanoma", "Vulvar melanoma", "vulva; melanoma", "VULVA, MELANOCARCINOMA", "mammalian vulva melanoma", "vulvar melanoma (disease)", "malignant melanoma of vulva", "MALIGNANT MELANOMA OF VULVA", "Malignant melanoma of vulva", "mammalian vulva melanoma (disease)", "melanoma (disease) of mammalian vulva", "Malignant melanoma of vulva (disorder)", "malignant melanoma of vulva (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vulvar melanoma", "shortest_name_length": 15}
{"curie": "MONDO:0014842", "names": ["MRD41", "autosomal dominant mental retardation 41", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 41", "mental retardation, autosomal dominant 41", "autosomal dominant intellectual disability 41", "intellectual disability, autosomal dominant 41", "mental retardation, autosomal dominant type 41", "intellectual disability, autosomal dominant type 41", "autosomal dominant intellectual developmental disorder 41", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 41", "autosomal dominant non-syndromic intellectual disability 41", "TBL1XR1 autosomal dominant non-syndromic intellectual disability", "autosomal dominant non-syndromic intellectual disability caused by mutation in TBL1XR1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 41", "shortest_name_length": 5}
{"curie": "UMLS:C3494425", "names": ["Mandibular Retroposition", "Retroposition, Mandibular", "Mandibular Retropositions", "Retropositions, Mandibular"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mandibular Retroposition", "shortest_name_length": 24}
{"curie": "UMLS:C0740346", "names": ["Malignant Fibrous Histiocytoma Metastatic", "Malignant fibrous histiocytoma metastatic", "HISTIOCYTOMA MALIGNANT FIBROUS METASTATIC", "Metastatic Malignant Fibrous Histiocytoma", "Metastatic Unclassified Pleomorphic Sarcoma", "Metastatic Undifferentiated Pleomorphic Sarcoma", "Metastatic Unclassified Pleomorphic Sarcoma (Formerly Metastatic \"MFH\")", "Metastatic Unclassified Pleomorphic Sarcoma (Formerly Metastatic \"Malignant Fibrous Histiocytoma\")"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant fibrous histiocytoma metastatic", "shortest_name_length": 41}
{"curie": "UMLS:C4525660", "names": ["Ileal Neuroendocrine Tumor by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ileal Neuroendocrine Tumor by AJCC v8 Stage", "shortest_name_length": 43}
{"curie": "MONDO:0015914", "names": ["primary orthostatic hypotension", "neurogenic orthostatic hypotension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary orthostatic hypotension", "shortest_name_length": 31}
{"curie": "MONDO:0004287", "names": ["Pancreatic Foamy Gland Adenocarcinoma", "pancreatic foamy gland adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pancreatic foamy gland adenocarcinoma", "shortest_name_length": 37}
{"curie": "UMLS:C1697450", "names": ["prominent epicanthal fold", "Prominent epicanthal folds", "prominent epicanthal fold (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prominent epicanthal folds", "shortest_name_length": 25}
{"curie": "MONDO:0012567", "names": ["AUTS12", "autism susceptibility 12", "autism, susceptibility to, 12", "AUTISM, SUSCEPTIBILITY TO, 12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autism, susceptibility to, 12", "shortest_name_length": 6}
{"curie": "MONDO:0018181", "names": ["SSSS", "Ritter", "Ritter Disease", "Ritter disease", "ritter disease", "Disease, Ritter", "ritters disease", "Ritters Disease", "Ritter's disease", "Ritter's Disease", "ritter's disease", "Disease, Ritter's", "scald skin syndrome", "Pemphigus neonatorum", "pemphigus neonatorum", "neonatorum; pemphigus", "scalded skin syndrome", "pemphigus; neonatorum", "skin scalded syndrome", "Scalded skin syndrome", "SCALDED SKIN SYNDROME", "scalded skin; syndrome", "syndrome; scalded skin", "scalding skin syndrome", "Ritter's-Lyells syndrome", "staph scalded skin syndrome", "SCALDED SKIN SYNDROME STAPH", "Pemphigus neonatorum (disorder)", "generalized exfoliative disease", "Generalized exfoliative disease", "pemphigus neonatorum (diagnosis)", "dermatitis exfoliativa neonatorum", "Dermatitis exfoliativa neonatorum", "exfoliation; dermatitis, neonatorum", "staphylococcal scalded skin syndrome", "Staphylococcal Scalded-Skin Syndrome", "Staphylococcal Scalded Skin Syndrome", "Staphylococcal scalded skin syndrome", "Scalded Skin Syndrome, Staphylococcal", "Scalded-Skin Syndrome, Staphylococcal", "Staphylococcal Scalded-Skin Syndromes", "Syndrome, Staphylococcal Scalded-Skin", "(Staphylococcal) Scalded skin syndrome", "Syndromes, Staphylococcal Scalded-Skin", "Scalded-Skin Syndromes, Staphylococcal", "SSSS - Staphylococcal scalded skin syndrome", "Toxic epidermal necrolysis, subcorneal type", "toxic epidermal necrolysis, subcorneal type", "Staphylococcal scalded skin syndrome (disorder)", "staphylococcal scalded skin syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "staphylococcal scalded skin syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0013819", "names": ["CSS2", "MRD14", "COFFIN-SIRIS SYNDROME 2", "COFFIN-SIRIS syndrome 2", "Coffin-Siris syndrome 2", "ARID1A-related BAFopathy", "ARID1A Coffin-Siris syndrome", "CHROMOSOME 1p36.11 DUPLICATION SYNDROME", "autosomal dominant mental retardation 14", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 14", "mental retardation, autosomal dominant 14", "autosomal dominant intellectual disability 14", "mental retardation, autosomal dominant type 14", "intellectual disability, autosomal dominant 14", "Coffin-Siris syndrome caused by mutation in ARID1A", "intellectual disability, autosomal dominant type 14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 14", "shortest_name_length": 4}
{"curie": "MONDO:0030475", "names": ["HTX11", "HETEROTAXY, VISCERAL, 11, AUTOSOMAL, WITH MALE INFERTILITY", "heterotaxy, visceral, 11, autosomal, with male infertility"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heterotaxy, visceral, 11, autosomal, with male infertility", "shortest_name_length": 5}
{"curie": "MONDO:0044923", "names": ["NPMc+ AML", "AML, NPM1 Mutation", "AML with Mutated NPM1", "AML with mutated NPM1", "AML, NPM1 gene mutation", "AML, Nucleophosmin Gene Mutation", "AML, Mutation of the Nucleophosmin Gene", "Acute Myeloid Leukemia with Mutated NPM1", "acute myeloid leukemia with mutated NPM1", "Acute myeloid leukemia with mutated NPM1", "Acute myeloid leukaemia with mutated NPM1", "Acute Myeloid Leukemia with NPM1 Mutation", "acute myeloid leukemia, NPM1 gene mutation", "acute myeloid leukemia with cytoplasmic nucleophosmin", "Acute Myeloid Leukemia with Cytoplasmic Nucleophosmin", "Acute myeloid leukemia with mutated NPM1 (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia with mutated NPM1", "shortest_name_length": 9}
{"curie": "MONDO:0042233", "names": ["Systemic candida", "candida systemic", "systemic candida", "candidas systemic", "Systemic moniliasis", "invasive candidiasis", "Candidiasis;systemic", "Systemic candidiasis", "disseminated candida", "Disseminated candida", "systemic candidiasis", "candidiasis systemic", "Invasive candidiasis", "systemic; candidiasis", "candidiasis; systemic", "Candidiasis, systemic", "Disseminated candidosis", "disseminated candidosis", "Disseminated Candidiasis", "disseminated candidiasis", "CANDIDIASIS DISSEMINATED", "Disseminated candidiasis", "candidiasis; disseminated", "disseminated; candidiasis", "Systemic candida infections", "systemic candida infections", "systemic candidiasis (diagnosis)", "Disseminated candidiasis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disseminated candidiasis", "shortest_name_length": 16}
{"curie": "UMLS:C4288558", "names": ["Oligodendroglioma, IDH-Mutant and 1p/19q-Codeleted", "Oligodendroglioma, IDH-mutant and 1p/19q-codeleted", "Oligodendroglioma, IDH Mutant and 1p/19q Codeleted"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oligodendroglioma, IDH-Mutant and 1p/19q-Codeleted", "shortest_name_length": 50}
{"curie": "MONDO:0000603", "names": ["cardiovascular system autoimmune disease", "autoimmune disease of cardiovascular system", "autoimmune disorder of cardiovascular system", "cardiovascular system hypersensitivity reaction type II disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune disorder of cardiovascular system", "shortest_name_length": 40}
{"curie": "MONDO:0003828", "names": ["malignant Somatotropinoma", "malignant somatotropinoma", "malignant pituitary somatotropinoma", "Malignant Pituitary Somatotrophinoma", "malignant pituitary Somatotrophinoma", "malignant somatotropinoma of pituitary", "malignant Somatotrophinoma of pituitary", "Malignant Somatotrophinoma of Pituitary", "malignant Growth hormone producing tumor", "Malignant Growth Hormone Producing Tumor", "malignant pituitary gland somatotropinoma", "malignant somatotropinoma of the pituitary", "Metastatic Growth Hormone-Producing PitNET", "Malignant Pituitary Gland Somatotrophinoma", "malignant pituitary gland Somatotrophinoma", "malignant somatotropinoma of pituitary gland", "malignant Somatotrophinoma of pituitary gland", "Malignant Somatotrophinoma of Pituitary Gland", "malignant somatotropinoma of the pituitary gland", "Malignant Somatotrophinoma of the Pituitary Gland", "malignant Somatotrophinoma of the pituitary gland", "Malignant Growth Hormone Producing Pituitary Tumor", "malignant Growth hormone producing pituitary tumor", "malignant Growth hormone secreting pituitary tumor", "Malignant Growth Hormone Secreting Pituitary Tumor", "Growth hormone producing pituitary gland carcinoma", "growth hormone-producing pituitary gland carcinoma", "Growth hormone-producing pituitary gland carcinoma", "Growth Hormone Producing Pituitary Gland Carcinoma", "Malignant Growth Hormone Secreting Tumor of Pituitary", "malignant Growth hormone producing pituitary neoplasm", "Malignant Growth Hormone Producing Pituitary Neoplasm", "malignant Growth hormone secreting tumor of pituitary", "malignant Growth hormone producing tumor of pituitary", "Malignant Growth Hormone Secreting Pituitary Neoplasm", "Metastatic Somatotroph Pituitary Neuroendocrine Tumor", "Malignant Growth Hormone Producing Tumor of Pituitary", "malignant Growth hormone secreting pituitary neoplasm", "malignant Growth hormone secreting pituitary gland tumor", "Malignant Growth Hormone Producing Neoplasm of Pituitary", "Malignant Growth Hormone Secreting Neoplasm of Pituitary", "malignant Growth hormone secreting neoplasm of pituitary", "malignant Growth hormone producing neoplasm of pituitary", "Malignant Growth Hormone Secreting Pituitary Gland Tumor", "malignant growth hormone secreting neoplasm of pituitary", "Malignant Growth Hormone Producing Pituitary Gland Tumor", "malignant Growth hormone producing pituitary gland tumor", "malignant Growth hormone producing tumor of the pituitary", "Malignant Growth Hormone Secreting Tumor of the Pituitary", "malignant Growth hormone secreting tumor of the pituitary", "Malignant Growth Hormone Producing Tumor of the Pituitary", "Malignant Growth Hormone Producing Pituitary Gland Neoplasm", "Malignant Growth Hormone Secreting Pituitary Gland Neoplasm", "malignant Growth hormone secreting tumor of pituitary gland", "malignant Growth hormone producing tumor of pituitary gland", "Malignant Growth Hormone Producing Tumor of Pituitary Gland", "malignant Growth hormone producing pituitary gland neoplasm", "malignant Growth hormone secreting pituitary gland neoplasm", "Malignant Growth Hormone Secreting Tumor of Pituitary Gland", "Malignant Growth Hormone Producing Neoplasm of the Pituitary", "malignant Growth hormone producing neoplasm of the pituitary", "Malignant Growth Hormone Secreting Neoplasm of the Pituitary", "malignant Growth hormone secreting neoplasm of the pituitary", "malignant Growth hormone producing neoplasm of pituitary gland", "Malignant Growth Hormone Secreting Neoplasm of Pituitary Gland", "Malignant Growth Hormone Producing Neoplasm of Pituitary Gland", "malignant Growth hormone secreting neoplasm of pituitary gland", "Malignant Growth Hormone Secreting Tumor of the Pituitary Gland", "malignant Growth hormone secreting tumor of the pituitary gland", "malignant Growth hormone producing tumor of the pituitary gland", "Malignant Growth Hormone Producing Tumor of the Pituitary Gland", "Malignant Growth Hormone Secreting Neoplasm of the Pituitary Gland", "malignant Growth hormone producing neoplasm of the pituitary gland", "malignant Growth hormone secreting neoplasm of the pituitary gland", "Malignant Growth Hormone Producing Neoplasm of the Pituitary Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "growth hormone-producing pituitary gland carcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0008146", "names": ["OI1", "Lobstein", "OI type 1", "OI, type 1", "OI, TYPE I", "Van der Hoeve", "Ekman syndrome", "Eddowes syndrome", "Lobstein Disease", "Lobstein disease", "Lobsteins Disease", "Disease, Lobstein", "Lobstein's Disease", "Disease, Lobstein's", "van de Hoeve syndrome", "Blue sclerae syndrome", "Adair-Dighton syndrome", "Van der Hoeve syndrome", "Ekman-Lobstein syndrome", "Spurway-Eddowes syndrome", "Van der Hoeve's syndrome", "Mild osteogenesis imperfecta", "mild osteogenesis imperfecta", "OSTEOGENESIS IMPERFECTA TARDA", "osteogenesis imperfecta tarda", "Osteogenesis Imperfecta Tarda", "Osteogenesis imperfecta tarda", "osteogenesis imperfecta type 1", "i imperfecta osteogenesis type", "Osteogenesis imperfecta type I", "Osteogenesis Imperfecta Tardas", "Osteogenesis Imperfecta Type I", "Osteogenesis imperfecta type 1", "osteogenesis imperfecta type I", "Osteogenesis Imperfecta, Type 1", "OSTEOGENESIS IMPERFECTA, TYPE I", "Osteogenesis imperfecta, type I", "osteogenesis imperfecta, type I", "Osteogenesis Imperfecta, Type I", "osteogenesis imperfecta, type 1", "Osteopsathyrosis idiopathica tarda", "Fragilitas ossium hereditaria tarda", "Osteogenesis imperfecta psathyrotica", "van der Hoeve syndrome with deafness", "Non-deforming osteogenesis imperfecta", "non-deforming osteogenesis imperfecta", "OSTEOGENESIS IMPERFECTA WITH BLUE SCLERAE", "Osteogenesis Imperfecta with Blue Sclerae", "Osteogenesis imperfecta type I (disorder)", "Osteogenesis imperfecta with blue sclerae", "osteogenesis imperfecta with blue sclerae", "osteogenesis imperfecta type I (diagnosis)", "classic non-deforming OI with blue sclerae", "Fragilitas ossium-blue sclerae-otosclerosis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteogenesis imperfecta type 1", "shortest_name_length": 3}
{"curie": "MONDO:0006556", "names": ["Hand Dermatosis", "hand dermatosis", "Hand Dermatoses", "Dermatosis, Hand", "Dermatoses, Hand"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hand dermatosis", "shortest_name_length": 15}
{"curie": "MONDO:0018266", "names": ["v-AT", "Ataxia-telangiectasia variant", "ATAXIA-TELANGIECTASIA VARIANT", "Ataxia telangiectasia variant", "Ataxia-Telangiectasia Variant", "ataxia - telangiectasia variant", "v-AT - ataxia telangiectasia variant", "Ataxia telangiectasia variant (disorder)", "Ataxia telangiectasia variant (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ataxia - telangiectasia variant", "shortest_name_length": 4}
{"curie": "MONDO:0005977", "names": ["Tabes dorsalis", "Tabes Spinalis", "tabes dorsalis", "TABES DORSALIS", "dorsalis tabes", "Tabes Dorsalis", "Spinalis, Tabes", "tabes; dorsalis", "dorsalis; tabes", "duchenne disease", "disease duchenne", "Duchennes Disease", "Duchenne's disease", "duchenne's disease", "TABETIC NEUROSYPHILIS", "Tabetic Neurosyphilis", "Tabetic neurosyphilis", "syphilitic myelopathy", "Neurosyphilis, Tabetic", "Posterior spinal sclerosis", "posterior spinal sclerosis", "dorsalis neurosyphilis tabes", "Tabes dorsalis - neurosyphilis", "tabes dorsalis - neurosyphilis", "Tabetic neurosyphilis (disorder)", "Syphilitic posterior spinal sclerosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tabes dorsalis", "shortest_name_length": 14}
{"curie": "MONDO:0032635", "names": ["MC1DN32", "nuclear type mitochondrial complex I deficiency 32", "mitochondrial complex 1 deficiency, nuclear type 32", "MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 32"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial complex 1 deficiency, nuclear type 32", "shortest_name_length": 7}
{"curie": "MONDO:0011927", "names": ["TA", "Angioblastoma", "tufted angioma", "angioma tufted", "Tufted angioma", "TUFTED ANGIOMA", "Tufted Angioma", "angioma, tufted", "Angioma, tufted", "ANGIOMA, TUFTED", "Tufted hemangioma", "tufted hemangioma", "Tufted Hemangioma", "tufted skin angioma", "Tufted Skin Angioma", "tufted angioma of skin", "Nakagawa angioblastoma", "Tufted Angioma of Skin", "Tufted angioma of skin", "Hypertrophic hemangioma", "adult tufted hemangioma", "tufted angioma (disease)", "tufted hemangioma of skin", "Tufted Hemangioma of Skin", "angioblastoma of Nakagawa", "Angioblastoma of Nakagawa", "Tufted angioma (disorder)", "Acquired tufted hemangioma", "tufted angioma of the skin", "Tufted Angioma of the Skin", "Tufted Hemangioma of the Skin", "tufted hemangioma of the skin", "Progressive capillary hemangioma", "Tufted angioma of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tufted angioma", "shortest_name_length": 2}
{"curie": "UMLS:C1332339", "names": ["Asbestos-Related Cancer", "Asbestos-Related Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Asbestos-Related Malignant Neoplasm", "shortest_name_length": 23}
{"curie": "MONDO:0035738", "names": ["Acquired Factor VII Deficiency", "acquired factor VII deficiency", "Acquired factor VII deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired factor VII deficiency", "shortest_name_length": 30}
{"curie": "UMLS:C4687514", "names": ["Metastatic Epithelioid Hemangioendothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Epithelioid Hemangioendothelioma", "shortest_name_length": 43}
{"curie": "MONDO:0020341", "names": ["PVNH", "Periventricular Heterotopia", "periventricular heterotopia", "Periventricular Heterotopias", "Heterotopia, Periventricular", "Periventricular Nodular Heterotopia", "Periventricular nodular heterotopia", "periventricular nodular heterotopia", "Nodular Heterotopia, Periventricular", "Periventricular neuronal heterotopia", "Heterotopia, Periventricular Nodular", "Periventricular Nodular Heterotopias", "PVNH - periventricular nodular heterotopia", "Periventricular nodular heterotopia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "periventricular nodular heterotopia", "shortest_name_length": 4}
{"curie": "MONDO:0002199", "names": ["Vulvar Chondroid Syringoma", "Benign Mixed Tumor of the Vulva", "benign mixed tumor of the vulva", "chondroid syringoma of the vulva", "Chondroid Syringoma of the Vulva"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign mixed tumor of the vulva", "shortest_name_length": 26}
{"curie": "MONDO:0024277", "names": ["Purpura neonatal", "Neonatal purpura", "PURPURA NEONATAL", "neonatal purpura", "purpura of newborn", "Purpura of newborn", "Neonatal thrombocytopenia", "Neonatal Thrombocytopenia", "THROMBOCYTOPENIA NEONATAL", "Thrombocytopenia neonatal", "neonatal thrombocytopenia", "thrombocytopenia; neonatal", "Neonatal thrombocytopenia (disorder)", "Thrombocytopenia, Neonatal Alloimmune"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal thrombocytopenia", "shortest_name_length": 16}
{"curie": "UMLS:C2981677", "names": ["Stage IIB Pancreatic Cancer", "Stage IIB Pancreatic Cancer AJCC v6 and v7", "Stage IIB Exocrine and Endocrine Pancreatic Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Pancreatic Cancer AJCC v6 and v7", "shortest_name_length": 27}
{"curie": "MONDO:0032637", "names": ["CILD39", "primary ciliary dyskinesia 39", "ciliary dyskinesia, primary, 39", "CILIARY DYSKINESIA, PRIMARY, 39", "primary ciliary dyskinesia 39 with or without situs inversus", "Ciliary Dyskinesia, Primary, 39, With or Without Situs Inversus", "CILIARY DYSKINESIA, PRIMARY, 39, WITH OR WITHOUT SITUS INVERSUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ciliary dyskinesia, primary, 39", "shortest_name_length": 6}
{"curie": "UMLS:C4053521", "names": ["HFLT", "Hemosiderotic Fibrolipomatous Tumor", "Hemosiderotic Fibrohistiocytic Lipomatous Lesion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hemosiderotic Fibrolipomatous Tumor", "shortest_name_length": 4}
{"curie": "UMLS:C4331975", "names": ["Stage IV HPV-Mediated (p16-Positive) Oropharyngeal Throat Cancer", "Pathologic Stage IV HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage IV HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8", "shortest_name_length": 64}
{"curie": "MONDO:0041656", "names": ["STEMI", "acute STEMI", "ST Elevated Myocardial Infarction", "ST-elevation myocardial infarction", "ST Elevation Myocardial Infarction", "ST elevation myocardial infarction", "ST segment elevation myocardial infarction", "ST Segment Elevation Myocardial Infarction", "STEMI - ST elevation myocardial infarction", "acute myocardial infarction with ST elevation", "Acute ST segment elevation myocardial infarction", "acute-ST segment elevation myocardial infarction", "acute myocardial infarction with ST elevation (diagnosis)", "Acute ST segment elevation myocardial infarction (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ST-elevation myocardial infarction", "shortest_name_length": 5}
{"curie": "MONDO:0017135", "names": ["olivopontocerebellar atrophy deafness", "olivopontocerebellar atrophy-deafness syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "olivopontocerebellar atrophy-deafness syndrome", "shortest_name_length": 37}
{"curie": "MONDO:0002096", "names": ["CM", "Conjunctiva Melanoma", "conjunctiva melanoma", "Conjunctival Melanoma", "conjunctival melanoma", "conjunctiva; melanoma", "Conjunctival melanoma", "melanoma; conjunctiva", "Melanoma of Conjunctiva", "melanoma of conjunctiva", "melanoma of the conjunctiva", "Melanoma of the Conjunctiva", "malignant conjunctiva melanoma", "Malignant Conjunctiva Melanoma", "conjunctiva melanoma (disease)", "conjunctival malignant melanoma", "malignant conjunctival melanoma", "Conjunctival malignant melanoma", "Malignant Conjunctival Melanoma", "malignant melanoma of conjunctiva", "Malignant melanoma of conjunctiva", "Malignant Melanoma of Conjunctiva", "melanoma (disease) of conjunctiva", "malignant melanoma of the conjunctiva", "Malignant Melanoma of the Conjunctiva", "conjunctival neoplasm malignant melanoma", "Malignant melanoma of conjunctiva (disorder)", "malignant melanoma of conjunctiva (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant conjunctival melanoma", "shortest_name_length": 2}
{"curie": "MONDO:0003976", "names": ["malignant type AB thymoma", "malignant thymoma type AB", "Malignant Type AB Thymoma", "thymoma type AB, malignant", "Thymoma, type AB, malignant", "Thymoma, mixed type, malignant", "thymoma, mixed type, malignant", "Thymoma, type AB, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant type AB thymoma", "shortest_name_length": 25}
{"curie": "UMLS:C5419563", "names": ["Refractory Malignant Lymphoid Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Malignant Lymphoid Neoplasm", "shortest_name_length": 38}
{"curie": "MONDO:0010344", "names": ["MRX45", "XLID45", "X-linked mental retardation 45", "Mental Retardation, X-Linked 45", "mental retardation, X-linked 45", "MENTAL RETARDATION, X-LINKED 45", "intellectual disability, X-linked 45", "mental retardation, X-linked type 45", "intellectual disability, X-linked type 45", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 45", "non-syndromic X-linked intellectual disability 45", "ZNF81 non-syndromic X-linked intellectual disability", "non-syndromic X-linked intellectual disability caused by mutation in ZNF81"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 45", "shortest_name_length": 5}
{"curie": "UMLS:C4682502", "names": ["Tumor Stage (Pathological)", "Uterine Corpus Cancer by AJCC v8 Stage", "Uterine Corpus Carcinoma or Carcinosarcoma by AJCC v8 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uterine Corpus Cancer by AJCC v8 Stage", "shortest_name_length": 26}
{"curie": "MONDO:0009644", "names": ["MOCODB", "MOCOD type B", "molybdenum cofactor deficiency B", "Molybdenum Cofactor Deficiency Type B", "molybdenum cofactor deficiency type B", "molybdenum cofactor deficiency complementation group B", "Molybdenum cofactor deficiency complementation group B", "molybdenum cofactor deficiency, complementation group B", "Molybdenum Cofactor Deficiency, Complementation Group B", "MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B", "molybdenum cofactor deficiency, complementation group type B", "Molybdenum cofactor deficiency complementation group B (disorder)", "sulfite oxidase deficiency due to molybdenum cofactor deficiency type B", "Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B", "Combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type B", "combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sulfite oxidase deficiency due to molybdenum cofactor deficiency type B", "shortest_name_length": 6}
{"curie": "MONDO:0019155", "names": ["Leydig cell agenesis", "Leydig Cell Hypoplasia", "Leydig cell hypoplasia", "Leydig cell hypoplasia (diagnosis)", "LH resistance due to LH receptor deactivation", "LH Resistance Due To LH Receptor Deactivation", "46,XY DSD due to LH resistance or LHB deficiency", "46,XY disorder of sex development due to LH defects", "Male hypergonadotropic hypogonadism due to LHCGR defect", "Male pseudohermaphroditism due to LH resistance or LHB deficiency", "46,XY disorder of sex development due to LH resistance or LHB deficiency", "46,XY DSD due to luteinizing hormone resistance or luteinizing hormone beta subunit deficiency", "Male pseudohermaphroditism due to luteinizing hormone resistance or luteinizing hormone beta subunit deficiency", "46,XY disorder of sex development due to luteinizing hormone resistance or luteinizing hormone beta subunit deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Leydig cell hypoplasia", "shortest_name_length": 20}
{"curie": "UMLS:C3251580", "names": ["Drug Induced Pancytopenia", "pancytopenia drug-induced", "Drug-Induced Pancytopenia", "Drug induced pancytopenia", "Pancytopenia due to medication", "Pancytopenia caused by medication", "pancytopenia drug-induced (diagnosis)", "Pancytopenia caused by medication (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancytopenia caused by medication", "shortest_name_length": 25}
{"curie": "MONDO:0004056", "names": ["Bladder Papillary Urothelial Carcinoma", "bladder urothelial papillary carcinoma", "bladder papillary urothelial carcinoma", "Urothelial Papillary Carcinoma of the Bladder", "urothelial papillary carcinoma of the bladder", "urinary bladder papillary transitional cell carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder papillary urothelial carcinoma", "shortest_name_length": 38}
{"curie": "UMLS:C0334336", "names": ["Adrenal Gland Mixed Cell Adenoma", "Mixed Cell Adrenocortical Adenoma", "Adrenal Cortex Mixed Cell Adenoma", "Mixed Cell Adrenal Cortex Adenoma", "Mixed Cell Adrenal Cortical Adenoma", "Adrenal Cortical Mixed Cell Adenoma", "Adrenal cortical adenoma, mixed cell", "adenoma; mixed cell, adrenal (cortex)", "mixed cell; adenoma, adrenal (cortex)", "Adrenal cortical adenoma - mixed cell", "Adrenal cortical adenoma, mixed cell type", "Adrenal cortical adenoma, mixed cell (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mixed Cell Adrenal Cortical Adenoma", "shortest_name_length": 32}
{"curie": "MONDO:0013108", "names": ["ALL", "All1", "leukemia, acute lymphoblastic", "leukemia, acute lymphoblastic, somatic", "leukemia, T-cell acute lymphocytic, somatic", "T-cell acute lymphoblastic leukemia, somatic", "leukemia, T-cell acute lymphoblastic, somatic", "leukemia, acute lymphocytic, susceptibility to, 1", "LEUKEMIA, ACUTE LYMPHOCYTIC, SUSCEPTIBILITY TO, 1", "LEUKEMIA, ACUTE LYMPHOBLASTIC, SUSCEPTIBILITY TO, 1", "leukemia, acute lymphoblastic, susceptibility to, 1", "LEUKEMIA, T-CELL ACUTE LYMPHOBLASTIC, SUSCEPTIBILITY TO", "leukemia, B-cell acute lymphoblastic, susceptibility to", "LEUKEMIA, B-CELL ACUTE LYMPHOBLASTIC, SUSCEPTIBILITY TO", "leukemia, T-cell acute lymphoblastic, susceptibility to", "leukemia, acute lymphoblastic, B-Hyperdiploid, susceptibility to", "LEUKEMIA, ACUTE LYMPHOBLASTIC, B-HYPERDIPLOID, SUSCEPTIBILITY TO", "leukemia, acute lymphocytic, Philadelphia chromosome positive, somatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukemia, acute lymphocytic, susceptibility to, 1", "shortest_name_length": 3}
{"curie": "MONDO:0008635", "names": ["abnormal uterus", "uterus abnormal", "uterus; anomaly", "anomaly; uterus", "uterine anomaly", "Abnormal uterus", "UTERINE ANOMALY", "anomalies uterus", "uterus anomalies", "Anomalous uterus", "Uterus, abnormal", "uterus; deformity", "Uterus, anomalous", "UTERINE ANOMALIES", "uterine anomalies", "deformity; uterus", "Uterine Anomalies", "anomalies uterine", "uterine abnormality", "abnormalities uterine", "Uterine malformations", "Uterine abnormalities", "UTERINE ABNORMALITY NOS", "UTERINE ABNORMALITY, NOS", "Abnormality of the uterus", "congenital anomaly uterus", "Congenital abnormal uterus", "Congenital uterine anomaly", "anomalies congenital uterus", "congenital uterus anomalies", "congenital anomalies uterus", "Congenital anomaly of uterus", "anomalies congenital uterine", "Congenital uterine anomaly NOS", "abnormality congenital uterine", "Congenital uterine disorder NOS", "Congenital abnormal uterus, NOS", "Congenital uterine anomaly, NOS", "congenital abnormality of uterus", "Congenital Uterine Abnormalities", "congenital uterine abnormalities", "Congenital abnormality of uterus", "CONGENITAL ANOMALIES OF THE UTERUS", "Congenital uterine anomaly (disorder)", "congenital abnormality of uterus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine anomalies", "shortest_name_length": 15}
{"curie": "MONDO:0011728", "names": ["BEB", "Spasm eyelid", "spasm eyelid", "Eyelid spasm", "eyelid spasm", "SPASM EYELID", "BLEPHAROSPASM", "twitch eyelid", "eyelid spasms", "eyelid twitch", "Blepharospasm", "blepharospasm", "blepharospasms", "Blepharospasms", "twitching eyelid", "Eyelid Twitching", "Spasm of Eyelids", "eyelid twitching", "Eyelid twitching", "Spasm of eyelids", "eyelids twitching", "Twitch(ing);eyelid", "Primary Blepharospasm", "blepharospasm was seen", "Blepharospasm syndrome", "Essential blepharospasm", "Essential Blepharospasm", "Blepharospasm (disorder)", "blepharospasm (diagnosis)", "Involuntary closure of eyelid", "blepharospasm, primary benign", "Spontaneous closure of eyelid", "benign essential blepharospasm", "Benign essential blepharospasm", "blepharospasm, benign essential", "Blepharospasm (spasm of eyelid)", "Blepharospasm, Benign Essential", "blepharospasm (physical finding)", "BLEPHAROSPASM, BENIGN ESSENTIAL, SUSCEPTIBILITY TO", "blepharospasm, benign essential, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blepharospasm", "shortest_name_length": 3}
{"curie": "UMLS:C0521760", "names": ["Fatigable Positional Nystagmus", "Fatigable positional nystagmus", "nystagmus fatigable positional", "Nystagmus, Fatigable Positional", "Fatigable positional nystagmus (disorder)", "Fatigable positional nystagmus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fatigable Positional Nystagmus", "shortest_name_length": 30}
{"curie": "MONDO:0022456", "names": ["ankle defects short stature"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ankle defects short stature", "shortest_name_length": 27}
{"curie": "MONDO:0005695", "names": ["HIV-associated CNS vasculitis", "HIV-Associated CNS Vasculitis", "CNS vasculitis, HIV associated", "CNS vasculitis, HIV-associated", "CNS Vasculitis, HIV-Associated", "Vasculitis, HIV-Associated CNS", "vasculitis, HIV-associated CNS", "CNS Vasculitis, HIV Associated", "HIV-1-Associated CNS Vasculitis", "HIV-1-associated CNS vasculitis", "HIV-associated CNS Vasculitides", "HIV 1 Associated CNS Vasculitis", "HIV-Associated CNS Vasculitides", "HIV 1 associated CNS vasculitis", "CNS vasculitis, HIV-1-associated", "CNS Vasculitides, HIV-Associated", "CNS Vasculitis, HIV-1-Associated", "Vasculitis, HIV-1-Associated CNS", "vasculitis, HIV-1-associated CNS", "Vasculitides, HIV-Associated CNS", "Vasculitides, HIV-associated CNS", "CNS Vasculitides, HIV-associated", "HIV-1-Associated CNS Vasculitides", "HIV-1-associated CNS Vasculitides", "CNS Vasculitides, HIV-1-Associated", "Vasculitides, HIV-1-Associated CNS", "CNS Vasculitides, HIV-1-associated", "Vasculitides, HIV-1-associated CNS", "Central Nervous System AIDS Arteritis", "central nervous system AIDS arteritis", "AIDS Arteritis, Central Nervous System", "AIDS-associated cerebral aneurysmal arteriopathy", "AIDS Associated Cerebral Aneurysmal Arteriopathy", "AIDS-Associated Cerebral Aneurysmal Arteriopathy", "AIDS associated cerebral aneurysmal arteriopathy", "cerebral aneurysmal arteriopathy, AIDS associated", "Cerebral Aneurysmal Arteriopathy, AIDS-Associated", "Cerebral Aneurysmal Arteriopathy, AIDS Associated", "cerebral aneurysmal arteriopathy, AIDS-associated", "HIV-associated vasculitis of the central nervous system", "HIV-Associated Vasculitis of the Central Nervous System", "HIV Associated Vasculitis of the Central Nervous System", "HIV associated vasculitis of the central nervous system", "vasculitis of the central nervous system, HIV-associated", "vasculitis of the central nervous system, HIV associated", "Vasculitis of the Central Nervous System, HIV Associated", "Vasculitis of the Central Nervous System, HIV-Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central nervous system AIDS arteritis", "shortest_name_length": 29}
{"curie": "UMLS:C4055372", "names": ["Bone Tumor of Undefined Neoplastic Nature"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bone Tumor of Undefined Neoplastic Nature", "shortest_name_length": 41}
{"curie": "MONDO:0006639", "names": ["ACC", "adrenal carcinoma", "ADRENAL CARCINOMA", "CARCINOMA ADRENAL", "Adrenal carcinoma", "Carcinoma adrenal", "carcinoma adrenal", "adrenal carcinomas", "adrenal cortex cancer", "adrenocortical cancer", "Adrenal carcinoma NOS", "Adrenal Cortex Cancer", "Adrenal gland carinoma", "Adrenal adenocarcinoma", "adrenal adenocarcinoma", "adenocarcinoma adrenal", "Cortical Cell Carcinoma", "Adrenal cortical tumors", "cortical cell carcinoma", "adrenal cortical tumors", "Adrenocortical carcinoma", "Adrenal Cortex Carcinoma", "adrenocortical carcinoma", "Adrenocortical Carcinoma", "adrenal cortex carcinoma", "Carcinoma, Adrenocortical", "Adrenocortical carcinomas", "Adrenocortical Carcinomas", "ADRENAL CORTEX, CARCINOMA", "carcinoma, adrenocortical", "adrenal cortical carcinoma", "Carcinomas, Adrenocortical", "Adrenal cortical carcinoma", "Adrenal Cortical Carcinoma", "carcinoma of adrenal gland", "neoplasm of adrenal cortex", "adrenal cortical; carcinoma", "Adrenal Cortical Carcinomas", "carcinoma; adrenal cortical", "Carcinoma of Adrenal Cortex", "Carcinoma, Adrenal Cortical", "carcinoma of adrenal cortex", "cancer of the adrenal cortex", "Adrenal carcinoma (disorder)", "Carcinomas, Adrenal Cortical", "Adrenal cortex adenocarcinoma", "Adrenal Cortex Adenocarcinoma", "adrenal cortex adenocarcinoma", "Adrenocortical carcinoma, NOS", "malignant adrenocortical tumor", "malignant Adrenocortical tumor", "carcinoma of the Adrenal cortex", "Adrenal cortical adenocarcinoma", "carcinoma of the adrenal cortex", "Carcinoma of the Adrenal Cortex", "adrenal cortical adenocarcinoma", "adenocarcinoma of adrenal gland", "Adrenal Cortical Adenocarcinoma", "adrenal cortical; adenocarcinoma", "ADRENAL CORTEX CANCER, CARCINOMA", "adenocarcinoma; adrenal cortical", "malignant tumour of adrenal cortex", "adrenocortical carcinoma (disease)", "CARCINOMA, ADRENOCORTICAL, MALIGNANT", "malignant neoplasm of adrenal cortex", "carcinoma, adrenocortical, malignant", "carcinoma of adrenal gland (diagnosis)", "Adenocarcinoma, Adrenocortical, Malignant", "adrenocortical carcinoma of adrenal gland", "adenocarcinoma, adrenocortical, malignant", "adenocarcinoma of adrenal gland (diagnosis)", "Adrenal cortical carcinoma (morphologic abnormality)", "adrenal cortical carcinoma (morphologic abnormality)", "adrenocortical carcinoma of adrenal gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adrenal cortex carcinoma", "shortest_name_length": 3}
{"curie": "UMLS:C1557335", "names": ["Ocular surface disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ocular surface disease", "shortest_name_length": 22}
{"curie": "UMLS:C2931320", "names": ["T cell immunodeficiency primary", "Primary T-Cell Immunodeficiency Disorders"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T cell immunodeficiency primary", "shortest_name_length": 31}
{"curie": "MONDO:0033864", "names": ["BAGOS", "NEDIMAE", "BAKER-GORDON SYNDROME", "Baker-Gordon syndrome", "Baker Gordon syndrome", "SYT1-related neurodevelopmental disorder", "Synaptotagmin 1-related neurodevelopmental disorder", "NEURODEVELOPMENTAL DISORDER WITH INVOLUNTARY MOVEMENT AND ABNORMAL ELECTROENCEPHALOGRAM", "Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome", "infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome", "Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome", "Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0003011", "names": ["carcinoma, renal, tubular, malignant", "renal mucinous tubular spindle cell carcinoma", "Renal mucinous tubular and spindle cell carcinoma", "Mucinous tubular and spindle cell renal carcinoma", "mucinous tubular and spindle cell renal carcinoma", "mucinous tubular and spindle renal cell carcinoma", "Mucinous Tubular and Spindle Cell Carcinoma of the Kidney", "mucinous tubular and spindle cell carcinoma of the kidney", "Renal mucinous tubular and spindle cell carcinoma (disorder)", "Renal mucinous tubular and spindle cell carcinoma (diagnosis)", "Renal mucinous tubular and spindle cell carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mucinous tubular and spindle renal cell carcinoma", "shortest_name_length": 36}
{"curie": "MONDO:0014267", "names": ["IMD15", "IMD15B", "immunodeficiency 15", "IMMUNODEFICIENCY 15B", "immunodeficiency 15B", "immunodeficiency type 15", "SCID due to IKK2 deficiency", "severe combined immunodeficiency due to IKK2 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe combined immunodeficiency due to IKK2 deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C1332909", "names": ["Cerebral Non-Hodgkin Lymphoma", "Cerebral Non-Hodgkin's Lymphoma", "Primary Cerebral Non-Hodgkin Lymphoma", "Primary Cerebral Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebral Non-Hodgkin Lymphoma", "shortest_name_length": 29}
{"curie": "UMLS:C0746402", "names": ["MANIC SYMPTOM", "manic symptom", "Manic symptom", "manic symptoms"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Manic symptom", "shortest_name_length": 13}
{"curie": "MONDO:0016929", "names": ["Trisomy Partial 8", "Partial trisomy 8", "Duplication of chromosome 8", "Chromosome 8, partial trisomy", "Partial trisomy of chromosome 8", "partial trisomy of chromosome 8", "partial duplication of chromosome 8", "Partial duplication of chromosome 8", "anomaly of chromosome 8 partial trisomy", "partial duplication of chromosome type 8", "Partial trisomy of chromosome 8 (disorder)", "Partial trisomy of chromosome 8 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of chromosome 8", "shortest_name_length": 17}
{"curie": "MONDO:0010054", "names": ["Spinal Muscular Atrophy with Mental Retardation", "SPINAL MUSCULAR ATROPHY WITH MENTAL RETARDATION", "spinal muscular atrophy with mental retardation", "spinal muscular atrophy with intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinal muscular atrophy with intellectual disability", "shortest_name_length": 47}
{"curie": "MONDO:0010607", "names": ["HTX1", "CHTD1", "LATERALITY, X-LINKED", "Visceral heterotaxia", "laterality, X-linked", "Laterality, X-linked", "ZIC3 visceral heterotaxy", "heterotaxy, visceral, X-linked", "Heterotaxy, visceral, X-linked", "X-linked visceral heterotaxy 1", "HETEROTAXY, VISCERAL, 1, X-LINKED", "heterotaxy, visceral, 1, X-linked", "Heterotaxy, Visceral, 1, X-Linked", "Dextrocardia with other cardiac malformations", "dextrocardia with Other Cardiac malformations", "DEXTROCARDIA WITH OTHER CARDIAC MALFORMATIONS", "visceral heterotaxy caused by mutation in ZIC3", "heterotaxy, visceral, 1, X-linked, X-linked recessive", "CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED", "congenital heart defects, multiple types, 1, X-linked", "situs inversus, Complex Cardiac defects, and splenic defects, X-linked", "Situs inversus, complex cardiac defects, and splenic defects, X-linked", "SITUS INVERSUS, COMPLEX CARDIAC DEFECTS, AND SPLENIC DEFECTS, X-LINKED", "congenital heart defects, nonsyndromic, 1, X-linked, X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heterotaxy, visceral, 1, X-linked", "shortest_name_length": 4}
{"curie": "MONDO:0019804", "names": ["tracheomalacia", "Tracheomalacia", "Floppy windpipe", "Tracheomalacias", "Type 1 tracheomalacia", "type 1 tracheomalacia", "Trachea Chondromalacia", "Trachea Chondromalacias", "Congenital tracheomalacia", "Tracheomalacia (disorder)", "Chondromalacia of Trachea", "congenital tracheomalacia", "Tracheomalacia, congenital", "congenital; tracheomalacia", "tracheomalacia; congenital", "tracheomalacia, congenital", "Congenital major airway collapse", "congenital major airway collapse", "Congenital tracheomalacia (disorder)", "congenital tracheomalacia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tracheomalacia", "shortest_name_length": 14}
{"curie": "UMLS:C0855077", "names": ["Stage IV Hodgkin's Disease Lymphocyte Predominance Type", "Hodgkin's disease lymphocyte predominance type stage IV"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hodgkin's disease lymphocyte predominance type stage IV", "shortest_name_length": 55}
{"curie": "UMLS:C0349009", "names": ["Septicemia candida", "candidiasis; sepsis", "Candidal septicemia", "Septicaemia candida", "Candidal septicaemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Septicaemia candida", "shortest_name_length": 18}
{"curie": "UMLS:C4520758", "names": ["Stage II Larynx Verrucous Carcinoma", "Stage II Laryngeal Verrucous Carcinoma", "Stage II Verrucous Carcinoma of Larynx", "Stage II Laryngeal Throat Verrucous Cancer", "Stage II Verrucous Carcinoma of the Larynx", "Stage II Laryngeal Verrucous Carcinoma AJCC v7", "Stage II Laryngeal Verrucous Carcinoma AJCC v6", "Stage II Laryngeal Verrucous Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Laryngeal Verrucous Carcinoma AJCC v6 and v7", "shortest_name_length": 35}
{"curie": "MONDO:0012785", "names": ["IHPS3", "Pyloric Stenosis, Infantile Hypertrophic, 3", "PYLORIC STENOSIS, INFANTILE HYPERTROPHIC, 3", "pyloric stenosis, infantile hypertrophic, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pyloric stenosis, infantile hypertrophic, 3", "shortest_name_length": 5}
{"curie": "MONDO:0018252", "names": ["focal palmoplantar keratoderma with joint keratoses"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "focal palmoplantar keratoderma with joint keratoses", "shortest_name_length": 51}
{"curie": "UMLS:C1336431", "names": ["Stage IV Ovarian Embryonal Carcinoma", "Ovarian Embryonal Carcinoma Stage IV", "Stage IV Ovarian Embryonal Carcinoma AJCC v7", "Stage IV Ovarian Embryonal Carcinoma AJCC v6", "Stage IV Ovarian Embryonal Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Ovarian Embryonal Carcinoma AJCC v6 and v7", "shortest_name_length": 36}
{"curie": "UMLS:C0276089", "names": ["E. coli pneumonia", "Pneumonia escherichia", "Pneumonia due to E. coli", "Escherichia coli pneumonia", "pneumonia; Escherichia coli", "Pneumonia caused by E. coli", "Escherichia coli; pneumonia", "Pneumonia due to Escherichia coli", "pneumonia due to Escherichia coli", "Pneumonia due to escherichia coli", "Pneumonia caused by Escherichia coli", "Escherichia coli (E. coli) pneumonia", "Pneumonia due to escherichia coli [E. coli]", "Pneumonia due to Escherichia coli (E. Coli)", "pneumonia due to Escherichia coli (diagnosis)", "Pneumonia caused by Escherichia coli (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pneumonia due to Escherichia coli", "shortest_name_length": 17}
{"curie": "MONDO:0023119", "names": ["Familial myelofibrosis", "familial myelofibrosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial myelofibrosis", "shortest_name_length": 22}
{"curie": "UMLS:C2697678", "names": ["Infectious Salpingitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infectious Salpingitis", "shortest_name_length": 22}
{"curie": "MONDO:0014571", "names": ["OPA8", "OPA9", "optic atrophy 9", "OPTIC ATROPHY 9", "OPTIC ATROPHY 8", "ACO2 autosomal recessive isolated optic atrophy", "autosomal recessive isolated optic atrophy caused by mutation in ACO2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "optic atrophy 9", "shortest_name_length": 4}
{"curie": "MONDO:0016555", "names": ["transient congenital hypothyroidism due to maternal factor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transient congenital hypothyroidism due to maternal factor", "shortest_name_length": 58}
{"curie": "MONDO:0022308", "names": ["CBGD", "Corticobasal Syndrome", "Corticobasal syndrome", "corticobasal syndrome", "corticobasal degeneration", "degeneration corticobasal", "Corticobasal Degeneration", "Corticobasal degeneration", "Cortico-basal Degeneration", "Cortico basal Degeneration", "corticobasal degeneration disorder", "Corticobasal degeneration (disorder)", "Cortico-basal Ganglionic Degeneration", "Cortico basal Ganglionic Degeneration", "corticobasal degeneration (diagnosis)", "cortical basal ganglionic degeneration", "Cortical basal ganglionic degeneration", "cortical-basal ganglionic degeneration", "Cortical Basal Ganglionic Degeneration", "cortico-basal ganglionic Degeneration (CBGD)", "Corticodentatonigral degeneration with neuronal achromasia", "corticodentatonigral degeneration with neuronal achromasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corticobasal degeneration disorder", "shortest_name_length": 4}
{"curie": "UMLS:C1610605", "names": ["Graft versus host disease of skin", "graft-versus-host disease of skin", "Graft versus host disease in skin", "Cutaneous graft-versus-host disease", "graft-versus-host disease (GVHD) of skin", "Graft versus host disease of skin (disorder)", "graft-versus-host disease of skin (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Graft versus host disease in skin", "shortest_name_length": 33}
{"curie": "MONDO:0004239", "names": ["Squamous Cell Carcinoma, Keratinizing", "cervical keratinizing squamous cell carcinoma", "Cervical Keratinizing Squamous Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cervical keratinizing squamous cell carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0002552", "names": ["vascular myelopathy", "Vascular myelopathy", "vascular; myelopathy", "myelopathy; vascular", "Vascular myelopathies", "vascular myelopathies", "Vascular myelopathy, NOS", "Vascular myelopathy (disorder)", "vascular myelopathies (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vascular myelopathy", "shortest_name_length": 19}
{"curie": "MONDO:0018977", "names": ["anti-MAG neuropathy", "Anti-MAG neuropathy", "polyneuropathy associated with IgM monoclonal gammapathy with anti-MAG", "Polyneuropathy associated with IgM monoclonal gammapathy with anti-MAG", "Neuropathy associated with monoclonal IgM antibodies to myelin-associated glycoprotein", "neuropathy associated with monoclonal IgM antibodies to myelin-associated glycoprotein"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyneuropathy associated with IgM monoclonal gammapathy with anti-MAG", "shortest_name_length": 19}
{"curie": "MONDO:0019396", "names": ["Collagen type III glomerulopathy", "collagen type III glomerulopathy", "Collagenofibrotic glomerulopathy", "Collagenofibrotic glomerulopathy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "collagen type III glomerulopathy", "shortest_name_length": 32}
{"curie": "UMLS:C0334332", "names": ["Adrenal Gland Compact Cell Adenoma", "Adrenal Cortex Compact Cell Adenoma", "Compact Cell Adrenal Cortex Adenoma", "Compact Cell Adrenocortical Adenoma", "Compact Cell Adrenal Cortical Adenoma", "Adrenal Cortical Compact Cell Adenoma", "Adrenal cortical adenoma, compact cell", "Adrenal cortical adenoma - compact cell", "Adrenal cortical adenoma, compact cell type", "Adrenal cortical adenoma, compact cell (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Compact Cell Adrenal Cortical Adenoma", "shortest_name_length": 34}
{"curie": "MONDO:0013250", "names": ["DFNB85", "autosomal recessive deafness 85", "deafness, autosomal recessive 85", "DEAFNESS, AUTOSOMAL RECESSIVE 85", "autosomal recessive nonsyndromic deafness 85", "autosomal recessive nonsyndromic hearing loss 85", "autosomal recessive nonsyndromic deafness type 85"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 85", "shortest_name_length": 6}
{"curie": "MONDO:0027652", "names": ["5-fluorouracil toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "5-fluorouracil toxicity", "shortest_name_length": 23}
{"curie": "UMLS:C1335458", "names": ["Stage III Hepatoblastoma", "Postsurgical Stage III Hepatoblastoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postsurgical Stage III Hepatoblastoma", "shortest_name_length": 24}
{"curie": "MONDO:0060713", "names": ["DCHE", "deafnes, congenital heart defects, and posterior embryotoxon", "deafness, congenital heart defects, and posterior embryotoxon", "DEAFNESS, CONGENITAL HEART DEFECTS, AND POSTERIOR EMBRYOTOXON", "Deafness, Congenital Heart Defects, and Posterior Embryotoxon"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness, congenital heart defects, and posterior embryotoxon", "shortest_name_length": 4}
{"curie": "MONDO:0016548", "names": ["megacystis-megaureter syndrome", "Megacystis-megaureter syndrome", "Megaureter-megacystis syndrome", "megaureter-megacystis syndrome", "Megacystis-megaureter syndrome (disorder)", "megacystis-megaureter syndrome (diagnosis)", "congenital anomaly of ureter megacystis-megaureter syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "megacystis-megaureter syndrome", "shortest_name_length": 30}
{"curie": "UMLS:C4527162", "names": ["Stage 0 Cutaneous (Skin) Melanoma", "Clinical Stage 0 Cutaneous Melanoma AJCC v8", "Clinical Stage 0 Melanoma of the Skin AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clinical Stage 0 Cutaneous Melanoma AJCC v8", "shortest_name_length": 33}
{"curie": "UMLS:C4553885", "names": ["Stage IVC Thyroid Gland Medullary Cancer", "Stage IVC Thyroid Gland Medullary Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVC Thyroid Gland Medullary Carcinoma AJCC v8", "shortest_name_length": 40}
{"curie": "MONDO:0016171", "names": ["polyradiculoneuropathy associated with IgG/IgA/IgM monoclonal gammopathy without known antibodies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polyradiculoneuropathy associated with IgG/IgA/IgM monoclonal gammopathy without known antibodies", "shortest_name_length": 97}
{"curie": "UMLS:C5555172", "names": ["Recurrent Ovarian Seromucinous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Ovarian Seromucinous Carcinoma", "shortest_name_length": 40}
{"curie": "UMLS:C4087161", "names": ["Human bocavirus infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Human bocavirus infection", "shortest_name_length": 25}
{"curie": "MONDO:0035018", "names": ["frontonasal dysplasia-bifid nose-upper limb anomalies syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontonasal dysplasia-bifid nose-upper limb anomalies syndrome", "shortest_name_length": 62}
{"curie": "MONDO:0015046", "names": ["Franklin", "Gamma-HCD", "gamma-HCD", "GAMMA HCD", "Franklin disease", "FRANKLIN DISEASE", "franklin disease", "Franklin Disease", "Franklins Disease", "heavy chain gamma", "franklins disease", "Franklin's disease", "Franklin's Disease", "franklin's disease", "GAMMA CHAIN DISEASE", "gamma-Chain Disease", "gamma Chain Disease", "gamma-Chain Diseases", "IGG HEAVY CHAIN DISEASE", "IgG heavy chain disease", "Gamma-heavy chain disease", "gamma heavy chain disease", "GAMMA HEAVY-CHAIN DISEASE", "Gamma Heavy Chain Disease", "Gamma heavy chain disease", "gamma-heavy chain disease", "heavy chain disease gamma", "Gamma heavy-chain disease", "disease; gamma heavy chain", "gamma heavy chain; disease", "Heavy chain disease, IgG type", "IgG heavy chain paraproteinemia", "Gamma heavy chain disease (disorder)", "Gamma heavy chain disease (clinical)", "Gamma heavy chain disease (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gamma-heavy chain disease", "shortest_name_length": 8}
{"curie": "MONDO:0001822", "names": ["HYPOLIPOPROTEINEMIA", "Hypolipoproteinemia", "hypolipoproteinemia", "Hypolipoproteinaemia", "Hypolipoproteinemias", "Lack of fat in blood", "hypolipoproteinaemia", "deficiency lipoprotein", "lipoprotein deficiency", "Lipoprotein deficiency", "deficiency; lipoprotein", "lipoprotein; deficiency", "lipoprotein deficiencies", "Lipoprotein deficiencies", "hypolipoproteinemia (disease)", "Hypolipoproteinemia (disorder)", "Lipoprotein deficiency disorder", "disorder; lipoprotein, deficiency", "lipoprotein deficiency (diagnosis)", "Lipoprotein deficiency disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypolipoproteinemia", "shortest_name_length": 19}
{"curie": "UMLS:C4553752", "names": ["Stage IV Prostate Cancer", "Stage IV Prostate Cancer AJCC v8", "Stage IV Prostate Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Prostate Cancer AJCC v8", "shortest_name_length": 24}
{"curie": "MONDO:0008905", "names": ["IMD103", "CANDF2", "CARD9 deficiency", "CARD9 IMMUNODEFICIENCY", "CARD9 immunodeficiency", "CANDIDIASIS, FAMILIAL, 2", "candidiasis, familial, 2", "Candidiasis, Familial, 2", "candidiasis, familial, type 2", "candidiasis, familial, 2, autosomal recessive", "invasive candidiasis-deep dermatophytosis syndrome", "Invasive candidiasis-deep dermatophytosis syndrome", "Invasive candidiasis, deep dermatophytosis syndrome", "IMMUNODEFICIENCY 103, SUSCEPTIBILITY TO FUNGAL INFECTIONS", "Candidiasis familial chronic mucocutaneous, autosomal recessive", "candidiasis familial chronic mucocutaneous, autosomal recessive", "Candidiasis, Familial Chronic Mucocutaneous, Autosomal Recessive", "CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL RECESSIVE", "candidiasis, familial chronic mucocutaneous, autosomal recessive", "predisposition to invasive fungal disease due to CARD9 deficiency", "Predisposition to invasive fungal disease due to CARD9 deficiency", "Predisposition to invasive fungal disease due to caspase recruitment domain family member 9 deficiency", "Predisposition to invasive fungal disease due to caspase recruitment domain family member 9 deficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "predisposition to invasive fungal disease due to CARD9 deficiency", "shortest_name_length": 6}
{"curie": "UMLS:C0079943", "names": ["Oral Fistula", "Oral fistula", "oral fistula", "oral fistulas", "Fistula, Oral", "Oral Fistulas", "fistula; oral", "oral; fistula", "Fistulas, Oral", "Oral fistula (disorder)", "oral fistula (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral Fistula", "shortest_name_length": 12}
{"curie": "MONDO:0010524", "names": ["ASAT", "Xlsa-A", "XLSA-A", "Pagon Bird Detter syndrome", "Pagon-Bird-Detter syndrome", "X-linked sideroblastic anemia and ataxia", "anemia, Sex-linked hypochromic Siderobla", "X-linked sideroblastic Anemia and ataxia", "X-Linked Sideroblastic Anemia and Ataxia", "Anemia, Sex-Linked Hypochromic Siderobla", "X-linked sideroblastic anemia with ataxia", "X-linked sideroblastic anaemia and ataxia", "X-linked sideroblastic anaemia with ataxia", "Anemia, sideroblastic spinocerebellar ataxia", "Anemia, sideroblastic, spinocerebellar ataxia", "anemia sideroblastic and spinocerebellar ataxia", "Anemia sideroblastic and spinocerebellar ataxia", "sideroblastic anemia with spinocerebellar ataxia", "Sideroblastic anemia with spinocerebellar ataxia", "anemia, sideroblastic, and spinocerebellar ataxia", "ANEMIA, SIDEROBLASTIC, AND SPINOCEREBELLAR ATAXIA", "Anemia, Sideroblastic, and Spinocerebellar Ataxia", "anemia, sideroblastic, with ataxia, X-linked recessive", "X-linked sideroblastic anemia and spinocerebellar ataxia", "X-linked sideroblastic anemia with spinocerebellar ataxia", "X-linked sideroblastic anaemia with spinocerebellar ataxia", "X-linked sideroblastic anemia with spinocerebellar ataxia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked sideroblastic anemia with ataxia", "shortest_name_length": 4}
{"curie": "MONDO:0005599", "names": ["epithelial mesothelioma", "Epithelial Mesothelioma", "Epithelioid mesothelioma", "mesothelioma, epithelial", "Epithelioid Mesothelioma", "epithelioid mesothelioma", "mesothelioma; epithelioid", "epithelioid; mesothelioma", "Epithelioid mesothelioma, NOS", "Malignant Epithelial Mesothelioma", "Epithelial malignant mesothelioma", "malignant epithelial mesothelioma", "malignant epithelioid mesothelioma", "Malignant epithelioid mesothelioma", "epithelioid mesothelioma, malignant", "Epithelioid mesothelioma, malignant", "epithelioid mesothelioma, malignant (morphologic abnormality)", "Epithelioid mesothelioma, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant epithelioid mesothelioma", "shortest_name_length": 23}
{"curie": "MONDO:0000931", "names": ["endometrial disease", "endometrium disease", "DISORDER ENDOMETRIAL", "endometrial disorder", "Endometrial Disorder", "ENDOMETRIAL DISORDER", "Disorder endometrial", "Endometrial disorder", "disease of endometrium", "disorder of endometrium", "Endometrial disorder NOS", "ENDOMETRIAL DISORDER (NOS)", "endometrium disease or disorder", "Endometrial disorder (disorder)", "disease or disorder of endometrium"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometrial disorder", "shortest_name_length": 19}
{"curie": "MONDO:0017726", "names": ["HEXOSAMINIDASE A DEFICIENCY, ADULT TYPE", "Hexosaminidase A deficiency, adult form", "hexosaminidase A deficiency, adult form", "Hexosaminidase A Deficiency, Adult Type", "Tay-Sachs disease, B variant, adult form", "GM2 gangliosidosis, B variant, adult form"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tay-Sachs disease, B variant, adult form", "shortest_name_length": 39}
{"curie": "UMLS:C4331296", "names": ["Small Cell Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Cell Adenocarcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0003953", "names": ["Childhood CNS Choriocarcinoma", "Pediatric CNS Choriocarcinoma", "childhood CNS choriocarcinoma", "pediatric CNS choriocarcinoma", "paediatric CNS choriocarcinoma", "Choriocarcinoma of Pediatric CNS", "Choriocarcinoma of Childhood CNS", "choriocarcinoma of pediatric CNS", "choriocarcinoma of childhood CNS", "Choriocarcinoma of the Pediatric CNS", "choriocarcinoma of the pediatric CNS", "Choriocarcinoma of the Childhood CNS", "choriocarcinoma of the childhood CNS", "Central nervous system choriocarcinoma", "Central Nervous System Choriocarcinoma", "childhood central nervous system choriocarcinoma", "pediatric central nervous system choriocarcinoma", "Pediatric Central Nervous System Choriocarcinoma", "Childhood Central Nervous System Choriocarcinoma", "choriocarcinoma of childhood central nervous system", "Choriocarcinoma of Pediatric Central Nervous System", "Choriocarcinoma of Childhood Central Nervous System", "choriocarcinoma of pediatric central nervous system", "childhood choriocarcinoma of the central nervous system", "Choriocarcinoma of the Pediatric Central Nervous System", "choriocarcinoma of the pediatric central nervous system", "Choriocarcinoma of the Childhood Central Nervous System", "pediatric choriocarcinoma of the central nervous system", "Choriocarcinoma of the pediatric central nervous system", "choriocarcinoma of the childhood central nervous system", "Choriocarcinoma of the paediatric central nervous system", "choriocarcinoma of the central nervous system of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pediatric CNS choriocarcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0003954", "names": ["Fordyce's spot", "Fordyce angiokeratoma", "Scrotal Angiokeratoma", "angiokeratoma scrotum", "Scrotal angiokeratoma", "Fordyce Angiokeratoma", "angiokeratoma fordyce", "fordyce angiokeratoma", "angiokeratomas scrotum", "angiokeratomas fordyce", "Angiokeratoma of Scrotum", "Angiokeratoma of Fordyce", "angiokeratoma of scrotum", "angiokeratoma of fordyce", "Angiokeratoma of scrotum", "angiokeratoma of Fordyce", "Angiokeratoma of the Scrotum", "Fordyce angiokeratoma of scrotum", "Scrotal Fordyce-Type Angiokeratoma", "Angiokeratoma of Fordyce (disorder)", "Angiokeratoma of Fordyce (diagnosis)", "Fordyce-type Angiokeratoma of scrotum", "Fordyce-Type Angiokeratoma of Scrotum", "Fordyce-type angiokeratoma of scrotum", "Fordyce-Type Angiokeratoma of the Scrotum", "Fordyce angiokeratoma of scrotum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "angiokeratoma of Fordyce", "shortest_name_length": 14}
{"curie": "MONDO:0042490", "names": ["SCN1", "severe congenital neutropenia 1", "neutropenia, severe congenital 1, autosomal dominant", "Neutropenia, Severe Congenital, Autosomal Dominant 1", "neutropenia, severe congenital, 1, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neutropenia, severe congenital, 1, autosomal dominant", "shortest_name_length": 4}
{"curie": "MONDO:0001101", "names": ["breast fat necrosis", "Breast Fat Necrosis", "fat necrosis breast", "breast Fat necrosis", "breasts fat necrosis", "BREAST, FAT NECROSIS", "fat necrosis of breast", "Fat Necrosis of Breast", "Fat necrosis of breast", "fat Necrosis of the breast", "Fat Necrosis of the Breast", "Fat necrosis of breast (disorder)", "fat necrosis of breast (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fat necrosis of breast", "shortest_name_length": 19}
{"curie": "UMLS:C4520751", "names": ["Stage I Sinonasal Cancer AJCC v6 and v7", "Stage I Sinonasal Carcinoma AJCC v6 and v7", "Stage I Nasal Cavity and Paranasal Sinus Cancer", "Stage I Nasal Cavity and Paranasal Sinus Cancer AJCC v6", "Stage I Nasal Cavity and Paranasal Sinus Cancer AJCC v7", "Stage I Nasal Cavity and Paranasal Sinus Cancer AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Nasal Cavity and Paranasal Sinus Cancer AJCC v6 and v7", "shortest_name_length": 39}
{"curie": "UMLS:C0341934", "names": ["hypertension pregnancy transient", "transient hypertension pregnancy", "Pregnancy Transient Hypertension", "Hypertension, Pregnancy Transient", "Transient Hypertension, Pregnancy", "pregnancy; hypertension, transient", "transient hypertension of pregnancy", "Transient hypertension of pregnancy", "Transient hypertension of pregnancy (disorder)", "pregnancy complicated by transient hypertension", "pregnancy complicated by transient hypertension (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Transient hypertension of pregnancy", "shortest_name_length": 32}
{"curie": "UMLS:C4553845", "names": ["Stage IV Thyroid Gland Medullary Cancer", "Stage IV Thyroid Gland Medullary Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Thyroid Gland Medullary Carcinoma AJCC v8", "shortest_name_length": 39}
{"curie": "MONDO:0014563", "names": ["ECHS1", "ECHS1D", "short-chain enoyl-CoA hydratase deficiency", "MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY", "Mitochondrial Short-Chain Enoyl-CoA Hydratase-1 Deficiency", "mitochondrial short-chain ENOYL-CoA hydratase 1 deficiency", "mitochondrial short-chain Enoyl-Coa hydratase 1 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mitochondrial short-chain Enoyl-Coa hydratase 1 deficiency", "shortest_name_length": 5}
{"curie": "UMLS:C1112366", "names": ["eyelid irritation", "Eyelid irritation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eyelid irritation", "shortest_name_length": 17}
{"curie": "MONDO:0010118", "names": ["THREONINEMIA", "threoninemia", "HYPERTHREONINEMIA", "hyperthreoninemia", "Hyperthreoninemia", "inherited threoninemia", "High blood threonine levels", "Elevated circulating threonine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited threoninemia", "shortest_name_length": 12}
{"curie": "MONDO:0002909", "names": ["hyperglycemia", "Hyperglycemia", "HYPERGLYCEMIA", "Hyperglycemias", "Hyperglycaemia", "HYPERGLYCAEMIA", "hyperglycaemia", "elevated glucose", "High blood sugar", "High Blood Sugar", "high blood sugar", "blood sugar; high", "high; blood sugar", "Hyperglycemia NOS", "sugar; blood, high", "High blood glucose", "Hyperglycemia, NOS", "High Blood Glucose", "blood; sugar, high", "Hyperglycaemia NOS", "Hyperglycaemia, NOS", "elevated blood sugar", "Elevated Blood Glucose", "hyperglycemic disorder", "Hyperglycemic disorder", "high blood sugar level", "Elevated blood glucose", "Hyperglycaemic disorder", "Hyperglycemia (disorder)", "hyperglycemia (diagnosis)", "Hyperglycemia, unspecified", "Hyperglycaemia, unspecified", "Hyperglycemic disorder (disorder)", "hyperglycemic disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperglycemia", "shortest_name_length": 13}
{"curie": "MONDO:0015719", "names": ["severe hemophilia A", "Severe hemophilia A", "Severe haemophilia A", "HEMOPHILIA A, SEVERE", "severe hemophilia type A", "severe factor VIII deficiency", "Severe congenital F8 deficiency", "Less than 1% of normal factor VIII", "Severe congenital factor VIII deficiency", "Severe hereditary factor VIII deficiency disease", "Severe hereditary factor VIII deficiency disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe hemophilia A", "shortest_name_length": 19}
{"curie": "MONDO:0016368", "names": ["RTS1", "Rothmund-Thomson syndrome type 1", "Rothmund-Thomson Syndrome Type 1", "Rothmund Thomson syndrome type 1", "ROTHMUND-THOMSON SYNDROME, TYPE 1", "Poikiloderma Atrophicans and Cataract", "poikiloderma of Rothmund-Thomson type 1", "Poikiloderma of Rothmund-Thomson type 1", "Rothmund Thomson syndrome type 1 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rothmund-Thomson syndrome type 1", "shortest_name_length": 4}
{"curie": "UMLS:C0278769", "names": ["Stage III CLL", "CLL Stage III", "CLL, stage III", "Chronic lymphocytic leukemia stage 3", "Chronic lymphocytic leukaemia stage 3", "stage III chronic lymphocytic leukemia", "Stage III Chronic Lymphocytic Leukemia", "Chronic Lymphocytic Leukemia Stage III", "lymphocytic leukemia, stage III chronic", "leukemia, stage III chronic lymphocytic", "chronic lymphocytic leukemia, stage III", "Stage III Chronic Lymphocytic Leukemia (CLL)", "Stage III Chronic Lymphocytic Leukemia- Modified Rai Staging System"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic lymphocytic leukemia stage 3", "shortest_name_length": 13}
{"curie": "MONDO:0004857", "names": ["Teninitis", "Tendonitis", "TENDONITIS", "tendinitis", "Tendinitis", "TENDINITIS", "tendonitis", "Tendonitides", "Tendinitides", "Tendinitis NOS", "Tendon inflamed", "Tendonitis, NOS", "Tendinitis, NOS", "tendon inflammation", "tendon; inflammation", "inflammation; tendon", "Tendinitis (disorder)", "inflammation of tendon", "tendonitis (diagnosis)", "tendon; disorder, inflammatory", "Inflammatory disorder of tendon", "disease (or disorder); tendon, inflammatory"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tendinitis", "shortest_name_length": 9}
{"curie": "MONDO:0015724", "names": ["non-distal trisomy 13q", "Non-distal trisomy 13q", "Non-telomeric trisomy 13q", "non-telomeric trisomy 13q", "non-distal duplication 13q", "Non-distal duplication 13q", "non-distal trisomy type 13q", "Non-distal trisomy 13q (disorder)", "Non-distal trisomy 13q (diagnosis)", "anomaly of chromosome pair 13 partial trisomy 13q non-distal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-distal trisomy 13q", "shortest_name_length": 22}
{"curie": "MONDO:0020648", "names": ["rubella encephalitis", "Rubella encephalitis", "ENCEPHALITIS, RUBELLA", "Rubella panencephalitis", "Rubella encephalitis (disorder)", "rubella encephalitis (diagnosis)", "Encephalitis due to rubella virus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rubella encephalitis", "shortest_name_length": 20}
{"curie": "MONDO:0009821", "names": ["RNS", "CSOCC", "Raine syndrome", "RAINE syndrome", "RAINE SYNDROME", "Raine dysplasia", "Raine dysplasia (disorder)", "Lethal osteosclerotic bone dysplasia", "lethal osteosclerotic bone dysplasia", "Osteosclerotic Bone Dysplasia, Lethal", "osteosclerotic bone dysplasia, lethal", "OSTEOSCLEROTIC BONE DYSPLASIA, LETHAL", "Osteomalacia, Sclerosing, with Cerebral Calcification", "OSTEOMALACIA, SCLEROSING, WITH CEREBRAL CALCIFICATION", "osteomalacia, sclerosing, with cerebral calcification", "[OBSOLETE] Osteomalacia, Sclerosing, with Cerebral Calcification", "combination of microcephaly, exophthalmos, hypoplastic nose and midface, gum hyperplasia, cleft palate, apparently low-set ears, and osteosclerosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal osteosclerotic bone dysplasia", "shortest_name_length": 3}
{"curie": "UMLS:C4525741", "names": ["Stage IV Colorectal Neuroendocrine Tumor", "Stage IV Colorectal Neuroendocrine Tumor AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Colorectal Neuroendocrine Tumor AJCC v8", "shortest_name_length": 40}
{"curie": "MONDO:0006375", "names": ["Chorangioma", "Chorangiomas", "Chorioangioma", "chorioangioma", "Chorioangiomas", "chorioangiomas", "placental angioma", "angioma; placenta", "placenta; angioma", "Placental Angioma", "Placental hamartoma", "Angioma of Placenta", "angioma of placenta", "placenta hemangioma", "placental hemangioma", "Placental hemangioma", "Placental Hemangioma", "Chorangioma placentae", "Chorangioma Placentae", "Hemangioma of Placenta", "hemangioma of placenta", "angioma of the placenta", "placental chorioangioma", "Placental chorioangioma", "Angioma of the Placenta", "Chorioangioma (disorder)", "Chorioangioma (diagnosis)", "hemangioma of the placenta", "Hemangioma of the Placenta", "Chorangioma of the placenta", "Chorangioma of the Placenta", "Chorangioma (morphologic abnormality)", "pregnancy complications chorioangioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "placental hemangioma", "shortest_name_length": 11}
{"curie": "MONDO:0013882", "names": ["GPIBD6", "HPMRS2", "glycosylphosphatidylinositol biosynthesis defect 6", "GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 6", "hyperphosphatasia with mental retardation syndrome 2", "PIGO hyperphosphatasia-intellectual disability syndrome", "hyperphosphatasia with mental retardation syndrome type 2", "hyperphosphatasia with intellectual disability syndrome 2", "hyperphosphatasia with intellectual disability syndrome type 2", "HYPERPHOSPHATASIA WITH IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME 2", "hyperphosphatasia with impaired intellectual development syndrome 2", "hyperphosphatasia-intellectual disability syndrome caused by mutation in PIGO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperphosphatasia with intellectual disability syndrome 2", "shortest_name_length": 6}
{"curie": "MONDO:0700197", "names": ["porcine leukemia", "Porcine Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "porcine leukemia", "shortest_name_length": 16}
{"curie": "MONDO:0032836", "names": ["WSKA", "WEISS-KRUSZKA SYNDROME", "weiss-kruszka syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "weiss-kruszka syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0007413", "names": ["CYPRUS facial neuromusculoskeletal syndrome", "CYPRUS FACIAL NEUROMUSCULOSKELETAL SYNDROME", "Cyprus facial neuromusculoskeletal syndrome", "Cyprus facial-neuromusculoskeletal syndrome", "Cyprus facial neuromusculoskeletal syndrome (disorder)", "unusual facial appearance, skeletal deformities, and musculoskeletal and sensory defects"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cyprus facial-neuromusculoskeletal syndrome", "shortest_name_length": 43}
{"curie": "UMLS:C4054394", "names": ["Nephrotic Syndrome - COQ2 Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - COQ2 Associated", "shortest_name_length": 36}
{"curie": "UMLS:C0265673", "names": ["Kyphosis", "kyphosis", "hunchback", "inborn hunchback", "Kyphosis congenital", "congenital kyphosis", "Congenital Kyphosis", "Congenital humpback", "Congenital kyphosis", "Kyphosis;congenital", "Congenital hunchback", "kyphosis; congenital", "congenital; kyphosis", "Kyphosis, congenital", "hunchback; congenital", "congenital; hunchback", "Congenital kyphosis (disorder)", "congenital kyphosis (diagnosis)", "congenital musculoskeletal deformity spine kyphosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital kyphosis", "shortest_name_length": 8}
{"curie": "MONDO:0044092", "names": ["Collagenous sprue", "Collagenous Sprue", "collagenous sprue", "Sprue, Collagenous", "collagenous Sprues", "Collagenous Sprues", "sprue, collagenous", "Sprues, Collagenous", "Sprues, collagenous", "Collagenous enteropathy", "collagenous enteropathy", "collagenous sprue (diagnosis)", "non-gluten intolerance syndrome", "Non-gluten intolerance syndrome", "Collagenous enteropathy syndrome", "collagenous enteropathy syndrome", "Non-gluten sensitive enteropathy syndrome", "non-gluten sensitive enteropathy syndrome", "Non-gluten sensitive enteropathy syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "collagenous sprue", "shortest_name_length": 17}
{"curie": "UMLS:C2931031", "names": ["PASH", "Pseudoangiomatous stromal hyperplasia", "Pseudoangiomatous Stromal Hyperplasia", "Breast Pseudoangiomatous Stromal Hyperplasia", "Mammary pseudoangiomatous stromal hyperplasia", "Pseudoangiomatous stromal hyperplasia of the breast", "Pseudoangiomatous stromal hyperplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pseudoangiomatous stromal hyperplasia", "shortest_name_length": 4}
{"curie": "MONDO:0035614", "names": ["sporadic fatal insomnia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sporadic fatal insomnia", "shortest_name_length": 23}
{"curie": "UMLS:C2984070", "names": ["Vaginal Cancer by AJCC v7 Stage", "Vaginal Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Cancer by AJCC v7 Stage", "shortest_name_length": 31}
{"curie": "MONDO:0006081", "names": ["anus melanoma", "Anal Melanoma", "anal melanoma", "melanoma; anus", "anus; melanoma", "melanoma of anus", "Melanoma of Anus", "Melanoma of the Anus", "melanoma of the anus", "Cancer anal melanoma", "Anal Malignant Melanoma", "malignant anus melanoma", "anus melanoma (disease)", "anal malignant melanoma", "melanoma (disease) of anus", "Malignant Melanoma of Anus", "Malignant melanoma of anus", "malignant melanoma of anus", "malignant melanoma of the anus", "Malignant Melanoma of the Anus", "Malignant melanoma of the anus", "Malignant melanoma of anus (disorder)", "malignant melanoma of anus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anal melanoma", "shortest_name_length": 13}
{"curie": "UMLS:C0677719", "names": ["Stage IV Indolent Non-Hodgkin Lymphoma", "Stage IV Indolent Adult Non-Hodgkin Lymphoma", "stage IV indolent adult non-Hodgkin lymphoma", "indolent, stage IV adult non-Hodgkin lymphoma", "stage IV indolent adult non-Hodgkin's lymphoma", "indolent stage IV adult non-Hodgkin's lymphoma", "indolent adult non-Hodgkin's lymphoma stage IV", "Stage IV Indolent Adult Non-Hodgkin's Lymphoma", "Indolent Stage IV Adult Non-Hodgkin's Lymphoma", "Indolent Adult Non-Hodgkin's Lymphoma Stage IV", "Ann Arbor Stage IV Indolent Adult Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Indolent Adult Non-Hodgkin Lymphoma", "shortest_name_length": 38}
{"curie": "MONDO:0006275", "names": ["GCLC", "Giant Cell Carcinoma", "giant cell carcinoma", "Giant cell carcinoma", "Cell Carcinoma, Giant", "Carcinoma, Giant Cell", "Giant Cell Carcinomas", "Cell Carcinomas, Giant", "Carcinomas, Giant Cell", "Lung Giant Cell Carcinoma", "giant cell lung carcinoma", "lung giant cell carcinoma", "Giant cell lung carcinoma", "Giant Cell Carcinoma of Lung", "Giant cell carcinoma of lung", "giant cell carcinoma of lung", "giant cell carcinoma of the lung", "giant cell carcinoma (diagnosis)", "Giant Cell Carcinoma of the Lung", "Giant cell carcinoma of lung (disorder)", "giant cell carcinoma of lung (diagnosis)", "Giant cell carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung giant cell carcinoma", "shortest_name_length": 4}
{"curie": "MONDO:0014545", "names": ["EMP8", "EPM8", "PME type 8", "progressive myoclonus epilepsy 8", "epilepsy, progressive myoclonic, 8", "EPILEPSY, PROGRESSIVE MYOCLONIC, 8", "CERS1 progressive myoclonic epilepsy", "progressive myoclonic epilepsy type 8", "Progressive myoclonus epilepsy type 8", "progressive myoclonus epilepsy type 8", "Progressive myoclonic epilepsy type 8", "epilepsy, progressive myoclonic, type 8", "progressive familial myoclonic epilepsy type 8", "Progressive myoclonic epilepsy type 8 (disorder)", "PME type 8 - progressive myoclonic epilepsy type 8", "progressive myoclonic epilepsy due to CERS1 deficiency", "Progressive myoclonic epilepsy due to CERS1 deficiency", "progressive myoclonic epilepsy caused by mutation in CERS1", "progressive familial myoclonic epilepsy type 8 (diagnosis)", "Progressive myoclonic epilepsy due to ceramide synthase 1 deficiency", "Progressive myoclonic epilepsy due to CERS1 (ceramide synthase 1) deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive myoclonic epilepsy type 8", "shortest_name_length": 4}
{"curie": "MONDO:0013718", "names": ["NPHP13", "NEPHRONOPHTHISIS 13", "nephronophthisis 13", "nephronophthisis type 13"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nephronophthisis 13", "shortest_name_length": 6}
{"curie": "MONDO:0020205", "names": ["bulbar conjunctival dermoid or conjunctival dermolipoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bulbar conjunctival dermoid or conjunctival dermolipoma", "shortest_name_length": 55}
{"curie": "UMLS:C2217678", "names": ["thyroid cancer stage III", "Thyroid cancer stage III", "malignant tumor of thyroid stage III", "malignant neoplasm of thyroid stage III", "malignant neoplasm of thyroid stage III (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thyroid cancer stage III", "shortest_name_length": 24}
{"curie": "UMLS:C2242657", "names": ["Metastatic Ocular Melanoma", "Metastatic ocular melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic ocular melanoma", "shortest_name_length": 26}
{"curie": "MONDO:0014493", "names": ["chai", "CHAI", "ALPS5", "IDAIL", "ALPS type 5", "ALPS type V", "CTLA4 Deficiency", "CTLA4 deficiency", "CTLA4 Haploinsufficiency", "CTLA4 haploinsufficiency", "ALPS due to CTLA4 haploinsuffiency", "autoimmune lymphoproliferative syndrome type V", "autoimmune lymphoproliferative syndrome type 5", "autoimmune lymphoproliferative syndrome, type V", "autoimmune lymphoproliferative syndrome, type 5", "AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V", "CTLA4 haploinsufficiency with autoimmune infiltration", "CTLA4 HAPLOINSUFFICIENCY WITH AUTOIMMUNE INFILTRATION", "CTLA-4 haploinsufficiency with autoimmune infiltration disease", "autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency", "Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency", "Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency", "immune dysregulation with autoimmunity, immunodeficiency, and lymphoproliferation", "IMMUNE DYSREGULATION WITH AUTOIMMUNITY, IMMUNODEFICIENCY, AND LYMPHOPROLIFERATION", "Autoimmune lymphoproliferative syndrome due to cytotoxic T-lymphocyte associated protein 4 haploinsufficiency", "Autoimmune lymphoproliferative syndrome due to cytotoxic T-lymphocyte associated protein 4 haploinsufficiency (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency", "shortest_name_length": 4}
{"curie": "MONDO:0000517", "names": ["brainstem medulloblastoma", "brain stem medulloblastoma", "medulloblastoma of brainstem"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brain stem medulloblastoma", "shortest_name_length": 25}
{"curie": "UMLS:C4744562", "names": ["Metastatic Lung Non-Small Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Lung Non-Small Cell Carcinoma", "shortest_name_length": 40}
{"curie": "UMLS:C4527009", "names": ["Stage IIIA Retroperitoneal Sarcoma", "Stage IIIA Retroperitoneal Sarcoma AJCC v8", "Stage IIIA Soft Tissue Retroperitoneal Sarcoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Retroperitoneal Sarcoma AJCC v8", "shortest_name_length": 34}
{"curie": "MONDO:0005835", "names": ["COCA 1", "Lynch syndrome", "Lynch Syndrome", "Syndrome, Lynch", "Lynch syndrome (disorder)", "Familial Nonpolyposis Colon Cancer", "Hereditary nonpolyposis colon cancer", "Hereditary non-polyposis colon cancer", "hereditary nonpolyposis colorectal cancer", "Hereditary non-polyposis colorectal cancer", "hereditary nonpolyposis colorectal neoplasm", "HNPCC - hereditary nonpolyposis colon cancer", "hereditary non-polyposis colon cancer type 1", "Hereditary Nonpolyposis Colorectal Neoplasms", "Hereditary Defective Mismatch Repair syndrome", "Colorectal Neoplasms, Hereditary Nonpolyposis", "hereditary defective mismatch repair syndrome", "Hereditary Defective Mismatch Repair Syndrome", "Hereditary nonpolyposis colon cancer syndrome", "Hereditary non-polyposis colon cancer syndrome", "Hereditary colorectal endometrial cancer syndrome", "Hereditary Colorectal Endometrial Cancer Syndrome", "Hereditary nonpolyposis colorectal cancer syndrome", "Hereditary non-polyposis colorectal cancer syndrome", "familial non-polyposis colon cancer (hMSH2, hMLH1, hPMS1, hPMS2)", "Familial Non-Polyposis Colon Cancer (hMSH2, hMLH1, hPMS1, hPMS2)", "Hereditary nonpolyposis colon cancer (hMSH2, hMLH1, hPMS1, hPMS2)", "Hereditary Nonpolyposis Colon Cancer (hMSH2, hMLH1, hPMS1, hPMS2)", "Hereditary Non-Polyposis Colon Cancer (hMSH2, hMLH1, hPMS1, hPMS2)", "Hereditary non-polyposis colon cancer (hMSH2, hMLH1, hPMS1, hPMS2)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lynch syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C5670621", "names": ["Central Nervous System Embryonal Tumor, NEC", "Central Nervous System Embryonal Tumor, Not Elsewhere Classified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System Embryonal Tumor, Not Elsewhere Classified", "shortest_name_length": 43}
{"curie": "MONDO:0006684", "names": ["brain wet", "wet brain", "edema brain", "Edema brain", "EDEMA BRAIN", "Brain edema", "Brain Edema", "brain swell", "brain edema", "BRAIN EDEMA", "brain; edema", "Edema, Brain", "brain oedema", "Brain oedema", "Oedema brain", "edema; brain", "Cerebral edema", "CEREBRAL EDEMA", "EDEMA CEREBRAL", "Brain swelling", "Edema cerebral", "brain swelling", "edema cerebral", "Cerebral Edema", "Brain Swelling", "swelling brain", "cerebral edema", "Brain Swellings", "cerebral oedema", "edema, cerebral", "Cerebral oedema", "Swelling, Brain", "OEDEMA CEREBRAL", "Edema, Cerebral", "brain swellings", "Oedema cerebral", "Swelling of brain", "intracranial edema", "Intracranial Edema", "Edema, Intracranial", "intracranial swelling", "Intracranial swelling", "Cerebral edema (disorder)", "cerebral edema (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "brain edema", "shortest_name_length": 9}
{"curie": "UMLS:C0740385", "names": ["aneurysm artery cerebral middle", "Middle Cerebral Artery Aneurysm", "Middle cerebral artery aneurysm", "middle cerebral artery aneurysm", "Aneurysm, Middle Cerebral Artery", "Aneurysm of middle cerebral artery", "aneurysm of middle cerebral artery", "Aneurysm of middle cerebral artery (disorder)", "aneurysm of middle cerebral artery (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aneurysm, Middle Cerebral Artery", "shortest_name_length": 31}
{"curie": "UMLS:C1512975", "names": ["Malignant Vaginal Mixed Tumor Resembling Synovial Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Vaginal Mixed Tumor Resembling Synovial Sarcoma", "shortest_name_length": 57}
{"curie": "UMLS:C1709553", "names": ["Pituitary Gland Neoplasm (Antiquated)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pituitary Gland Neoplasm (Antiquated)", "shortest_name_length": 37}
{"curie": "MONDO:0018813", "names": ["high grade B-cell lymphoma with MYC and/ or BCL2 and/or BCL6 rearrangement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "high grade B-cell lymphoma with MYC and/ or BCL2 and/or BCL6 rearrangement", "shortest_name_length": 74}
{"curie": "UMLS:C0278676", "names": ["Renal cancer stage II", "stage II kidney cancer", "Hypernephroma stage II", "stage II hypernephroma", "Kidney cancer stage II", "hypernephroma, stage II", "kidney cancer, stage II", "Renal carcinoma stage II", "Carcinoma kidney stage II", "Kidney carcinoma stage II", "stage II renal cell cancer", "Stage II Renal Cell Cancer", "renal cell cancer, stage II", "stage II renal cell carcinoma", "Renal cell carcinoma stage II", "renal cell carcinoma, stage II", "Renal Cell Cancer Stage II AJCC v6", "Stage II Renal Cell Cancer AJCC v6", "Stage II Renal Cell Carcinoma AJCC v6", "Renal Cell Carcinoma, Stage II AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Renal Cell Cancer", "shortest_name_length": 21}
{"curie": "MONDO:0008566", "names": ["FTC", "NMTC2", "Follicular thyroid cancer", "thyroid cancer, follicular", "Thyroid cancer, follicular", "Follicular Cancer of Thyroid", "thyroid carcinoma, follicular", "thyroid cancer, nonmedullary, 2", "THYROID CANCER, NONMEDULLARY, 2", "Follicular Cancer of the Thyroid", "Follicular Cancer of Thyroid Gland", "thyroid cancer, nonmedullary, type 2", "Follicular Cancer of the Thyroid Gland", "thyroid carcinoma, follicular, somatic", "thyroid carcinoma, follicular, autosomal dominant, somatic mutation", "thyroid cancer, nonmedullary, 2, autosomal dominant, somatic mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid cancer, nonmedullary, 2", "shortest_name_length": 3}
{"curie": "UMLS:C4525266", "names": ["Stage IV Intrahepatic Bile Duct Cancer", "Stage IV Intrahepatic Bile Duct Cancer AJCC v8", "Stage IV Intrahepatic Bile Duct Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Intrahepatic Bile Duct Cancer AJCC v8", "shortest_name_length": 38}
{"curie": "UMLS:C0019385", "names": ["Herpetic meningoencephalitis", "Herpetic Meningoencephalitis", "Meningoencephalitis herpetic", "Meningoencephalitis, Herpetic", "MENINGOENCEPHALITIS, HERPETIC", "Herpetic Meningoencephalitides", "Meningoencephalitides, Herpetic", "Herpes simplex meningoencephalitis", "Herpes Simplex Meningoencephalitis", "Meningoencephalitis, Herpes Simplex", "Herpes Simplex Meningoencephalitides", "Meningoencephalitides, Herpes Simplex", "Herpetic meningoencephalitis (disorder)", "Meningoencephalitis, Herpes Simplex Virus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Herpetic meningoencephalitis", "shortest_name_length": 28}
{"curie": "UMLS:C1333425", "names": ["Epithelioid Sarcoma NCI Grade 3", "Epithelioid Sarcoma NCI Grade III"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epithelioid Sarcoma NCI Grade 3", "shortest_name_length": 31}
{"curie": "UMLS:C5239029", "names": ["Locally Advanced High Grade Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced High Grade Sarcoma", "shortest_name_length": 35}
{"curie": "UMLS:C3899643", "names": ["Rectal Cancer", "Childhood Rectal Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Rectal Carcinoma", "shortest_name_length": 13}
{"curie": "UMLS:C1336430", "names": ["Stage IV Osteosarcoma", "Stage IV Osteogenic Sarcoma", "Stage IV Osteosarcoma AJCC v7", "Stage IV Osteosarcoma  AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Osteosarcoma AJCC v7", "shortest_name_length": 21}
{"curie": "UMLS:C0561596", "names": ["BITE WOUND DOG", "dog bite wound", "Dog bite wound", "bite dog wounds", "dog bite - wound", "Dog bite - wound", "Dog bite - wound (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dog bite - wound", "shortest_name_length": 14}
{"curie": "UMLS:C0580174", "names": ["Portal hypertensive gastropathy", "hypertensive portal gastropathy", "Portal hypertensive gastropathy (disorder)", "hypertensive portal gastropathy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Portal hypertensive gastropathy", "shortest_name_length": 31}
{"curie": "MONDO:0004139", "names": ["anemia normocytic", "Anemia normocytic", "NORMOCYTIC ANEMIA", "normocytic anemia", "Normocytic anemia", "ANEMIA NORMOCYTIC", "normocytic Anemia", "Normocytic Anemia", "normocytic anaemia", "ANAEMIA NORMOCYTIC", "Normocytic anaemia", "anemia; normocytic", "normocytic; anemia", "Anaemia normocytic", "Normocytic anemia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "normocytic anemia", "shortest_name_length": 17}
{"curie": "UMLS:C4727408", "names": ["Recurrent Parotid Gland Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Parotid Gland Carcinoma", "shortest_name_length": 33}
{"curie": "UMLS:C1332242", "names": ["Ameloblastic Carcinoma Ex Odontogenic Cyst", "Ameloblastic Carcinoma Derived From Odontogenic Cyst"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ameloblastic Carcinoma Derived From Odontogenic Cyst", "shortest_name_length": 42}
{"curie": "UMLS:C0553656", "names": ["Acute peritonsillitis", "peritonsillar cellulitis", "Peritonsillar cellulitis", "cellulitis; peritonsillar", "peritonsillar; cellulitis", "cellulitis of peritonsillar region", "Peritonsillar cellulitis (disorder)", "cellulitis of peritonsillar region (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peritonsillar cellulitis", "shortest_name_length": 21}
{"curie": "MONDO:0020289", "names": ["congenital tricuspid malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital tricuspid malformation", "shortest_name_length": 33}
{"curie": "MONDO:0016385", "names": ["Cantalamessa Baldini Ambrosi syndrome", "Cantalamessa-Baldini-Ambrosi syndrome", "hypogonadism-mitral valve prolapse-intellectual disability syndrome", "Hypogonadism-mitral valve prolapse-intellectual disability syndrome", "Hypogonadism with mitral valve prolapse and intellectual disability syndrome", "hypogonadism with mitral valve prolapse and intellectual disability syndrome", "primary gonadal failure, short stature, mitral valve prolapse, and mental retardation", "Primary gonadal failure, short stature, mitral valve prolapse, and mental retardation", "Hypogonadism with mitral valve prolapse and intellectual disability syndrome (disorder)", "hypogonadism with mitral valve prolapse and intellectual disability syndrome (diagnosis)", "primary gonadal failure, short stature, mitral valve prolapse, and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypogonadism-mitral valve prolapse-intellectual disability syndrome", "shortest_name_length": 37}
{"curie": "MONDO:0012093", "names": ["HPC3", "Prostate Cancer, Hereditary, 3", "PROSTATE CANCER, HEREDITARY, 3", "prostate cancer, hereditary, 3", "prostate cancer, hereditary, type 3", "prostate cancer, susceptibility to, 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate cancer, hereditary, 3", "shortest_name_length": 4}
{"curie": "MONDO:0011563", "names": ["GGF2", "HGF2", "GINGF2", "gingival fibromatosis, 2", "FIBROMATOSIS, GINGIVAL, 2", "Fibromatosis, Gingival, 2", "fibromatosis, gingival, 2", "hereditary gingival fibromatosis, 2", "fibromatosis gingival, hereditary, 2", "FIBROMATOSIS, GINGIVAL, HEREDITARY, 2", "Fibromatosis, Gingival, Hereditary, 2", "fibromatosis, gingival, hereditary, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibromatosis, gingival, 2", "shortest_name_length": 4}
{"curie": "MONDO:0001760", "names": ["Photokeratitis", "photokeratitis", "Ultraviolet Keratitis", "ultraviolet keratitis", "Photokeratitis (disorder)", "photokeratitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "photokeratitis", "shortest_name_length": 14}
{"curie": "UMLS:C5447550", "names": ["ICI-Induced Dermatitis", "Immune Checkpoint Inhibitor-Induced Dermatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Immune Checkpoint Inhibitor-Induced Dermatitis", "shortest_name_length": 22}
{"curie": "MONDO:0018525", "names": ["Solid pseudopapillary carcinoma", "pancreatic solid pseudopapillary carcinoma", "Pancreatic solid pseudopapillary carcinoma", "Pancreatic Solid Pseudopapillary Carcinoma", "solid pseudopapillary carcinoma of pancreas", "Solid Pseudopapillary Carcinoma of Pancreas", "Solid pseudopapillary carcinoma of pancreas", "Solid pseudopapillary neoplasm of the pancreas", "solid pseudopapillary neoplasm of the pancreas", "solid pseudopapillary carcinoma of the pancreas", "Solid Pseudopapillary Carcinoma of the Pancreas", "Solid pseudopapillary carcinoma of pancreas (disorder)", "solid pseudopapillary carcinoma of pancreas (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "solid pseudopapillary carcinoma of pancreas", "shortest_name_length": 31}
{"curie": "MONDO:0000758", "names": ["angiomatosis bacillary", "Bacillary angiomatosis", "Bacillary Angiomatosis", "bacillary Angiomatoses", "Bacillary Angiomatoses", "Angiomatosis bacillary", "bacillary angiomatosis", "angiomatoses, bacillary", "Angiomatosis, Bacillary", "Bartonella angiomatosis", "Angiomatoses, Bacillary", "Epithelioid Angiomatoses", "epithelioid Angiomatoses", "Epithelioid Angiomatosis", "epithelioid angiomatosis", "Angiomatoses, Epithelioid", "angiomatoses, epithelioid", "angiomatosis, epithelioid", "Angiomatosis, Epithelioid", "Bartonella caused angiomatosis", "Bacillary angiomatosis (disorder)", "Bacillary angiomatosis (diagnosis)", "bacillary epithelioid Angiomatoses", "Bacillary Epithelioid Angiomatoses", "bacillary epithelioid angiomatosis", "Bacillary Epithelioid Angiomatosis", "Epithelioid Angiomatoses, Bacillary", "epithelioid angiomatosis, bacillary", "angiomatosis, bacillary epithelioid", "epithelioid Angiomatoses, bacillary", "Angiomatoses, Bacillary Epithelioid", "Epithelioid Angiomatosis, Bacillary", "angiomatoses, bacillary epithelioid", "Angiomatosis, Bacillary Epithelioid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bacillary angiomatosis", "shortest_name_length": 22}
{"curie": "UMLS:C1541273", "names": ["Recurrent Marginal Zone Lymphoma", "Marginal zone lymphoma recurrent", "recurrent marginal zone lymphoma", "Recurrent Marginal Zone B-Cell Lymphoma", "recurrent marginal zone B-cell lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Marginal zone lymphoma recurrent", "shortest_name_length": 32}
{"curie": "MONDO:0020479", "names": ["giant", "Giant", "giants", "Launois", "giantism", "Giantism", "Gigantism", "GIGANTISM", "gigantism", "Giant, NOS", "Gigantosoma", "Normal giant", "Giantism, NOS", "Genetic giant", "genetics giant", "Giant, genetic", "Gigantism, NOS", "Primordial giant", "Launois syndrome", "Launois' syndrome", "gigantism disorder", "pituitary gigantism", "Pituitary Gigantism", "Pituitary gigantism", "gigantism was noted", "Gigantism (disorder)", "GIGANTISM, PITUITARY", "gigantism; pituitary", "pituitary; gigantism", "Gigantism, Pituitary", "Acromegalic gigantism", "hypophyseal gigantism", "Hypophyseal gigantism", "gigantism (diagnosis)", "Hypersomatotropic gigantism", "gigantism (physical finding)", "Hypersomatotropic gigantism (disorder)", "Infantile and juvenile forms of acromegaly", "infantile and juvenile forms of acromegaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pituitary gigantism", "shortest_name_length": 5}
{"curie": "UMLS:C0751956", "names": ["acute cva", "Acute Stroke", "stroke acute", "acute stroke", "Acute stroke", "CVA NOS ACUTE", "Acute Strokes", "Stroke, Acute", "stroke - acute", "Strokes, Acute", "Acute stroke (diagnosis)", "Acute Cerebrovascular Accident", "Acute cerebrovascular accident", "Acute Cerebrovascular Accidents", "Cerebrovascular Accident, Acute", "Cerebrovascular Accidents, Acute", "Acute cerebrovascular accident (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute Cerebrovascular Accidents", "shortest_name_length": 9}
{"curie": "MONDO:0024283", "names": ["Demodicosis", "demodicosis", "Demodecosis", "Demodicidosis", "Demodectic mange", "Follicular mange", "demodectic mange", "demodex infestation", "Demodex folliculitis", "Demodectic red mange", "infestation; Demodex", "Demodex; infestation", "Infestation by Demodex", "hair follicle demodicidosis", "Infestation by Demodex, NOS", "Infestation caused by Demodex", "Demodex folliculitis (disorder)", "Demodex folliculitis (diagnosis)", "Infestation caused by Demodex (disorder)", "dermatitis exogenous demodex folliculitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Demodex folliculitis", "shortest_name_length": 11}
{"curie": "MONDO:0004566", "names": ["Jejunal syndrome", "Post-cibal syndrome", "postgastrectomy syndrome", "POSTGASTRECTOMY SYNDROME", "Postgastrectomy Syndrome", "Postgastrectomy syndrome", "postgastrectomy; syndrome", "syndrome; postgastrectomy", "syndrome post gastrectomy", "POST GASTRECTOMY SYNDROME", "Post gastrectomy syndrome", "post gastrectomy syndrome", "Postgastrectomy syndromes", "Postgastrectomy Syndromes", "Syndrome, Postgastrectomy", "Syndromes, Postgastrectomy", "postgastric surgery syndrome", "Postgastric surgery syndrome", "Post gastric surgery syndrome", "Postgastric surgery syndromes", "post gastric surgery syndrome", "postgastrectomy syndrome (diagnosis)", "Postgastric surgery syndrome (disorder)", "postgastric surgery syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postgastrectomy syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0044337", "names": ["Stromal Sarcoma", "Stromal sarcoma", "stromal sarcoma", "sarcoma; stromal", "stromal; sarcoma", "Malignant stromal tumor", "Stromal Tumor, Malignant", "Malignant stromal tumour", "stromal tumor, malignant", "STROMAL SARCOMA, MALIGNANT", "stromal sarcoma, malignant", "stromal sarcoma (diagnosis)", "Stromal sarcoma (morphologic abnormality)", "Malignant stromal tumor (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stromal sarcoma", "shortest_name_length": 15}
{"curie": "UMLS:C3665732", "names": ["FS-DFSP", "Fibrosarcomatous DFSP", "Fibrosarcomatous DFSPs", "DFSP, Fibrosarcomatous", "DFSPs, Fibrosarcomatous", "Sarcomatous dermatofibrosarcoma", "Metastatic Dermatofibrosarcoma Protuberan", "Metastatic Dermatofibrosarcoma Protuberans", "Protuberan, Metastatic Dermatofibrosarcoma", "Dermatofibrosarcoma Protuberan, Metastatic", "Dermatofibrosarcoma protuberans metastatic", "Protuberans, Metastatic Dermatofibrosarcoma", "Dermatofibrosarcoma Protuberans, Metastatic", "Fibrosarcomatous Dermatofibrosarcoma Protuberan", "Protuberan, Fibrosarcomatous Dermatofibrosarcoma", "Fibrosarcomatous dermatofibrosarcoma protuberans", "Fibrosarcomatous Dermatofibrosarcoma Protuberans", "Dermatofibrosarcoma Protuberan, Fibrosarcomatous", "Dermatofibrosarcoma Protuberans, Fibrosarcomatous", "Protuberans, Fibrosarcomatous Dermatofibrosarcoma", "Fibrosarcomatous dermatofibrosarcoma protuberans (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Dermatofibrosarcoma Protuberans", "shortest_name_length": 7}
{"curie": "MONDO:0023043", "names": ["ectodermal dysplasia alopecia preaxial polydactyly", "Ectodermal dysplasia alopecia preaxial polydactyly", "absence of body & scalp hair, rounded nails, thin dental enamel, preaxial polydactyly of the feet, and unusual facial appearance", "Absence of body & scalp hair, rounded nails, thin dental enamel, preaxial polydactyly of the feet, and unusual facial appearance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia alopecia preaxial polydactyly", "shortest_name_length": 50}
{"curie": "UMLS:C4525399", "names": ["IIIA", "stage IIIA distal bile duct cancer", "stage IIIA distal bile duct cancer AJCC v8", "Stage IIIA Distal Bile Duct Cancer AJCC v8", "Stage IIIA Distal Bile Duct Carcinoma AJCC v8", "stage IIIA extrahepatic distal bile duct cancer", "Stage IIIA Extrahepatic (Distal) Bile Duct Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Distal Bile Duct Cancer AJCC v8", "shortest_name_length": 4}
{"curie": "UMLS:C3642304", "names": ["Placental Malformation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Placental Malformation", "shortest_name_length": 22}
{"curie": "MONDO:0024246", "names": ["Eccrine Poromatosis", "Acrosyringeal nevus", "acrosyringeal nevus", "Acrosyringeal Nevus", "Syringofibroadenoma", "syringofibroadenoma", "Acrosyringeal naevus", "Syringofibroadenomas", "Linear Eccrine Poroma", "Acrosyringeal Adenomatosis", "acrosyringeal adenomatosis", "Acrosyringeal adenomatosis", "eccrine syringofibroadenoma", "Eccrine Syringofibroadenoma", "Eccrine syringofibroadenoma", "Acrosyringeal nevus (disorder)", "eccrine syringofibroadenoma of skin", "Eccrine syringofibroadenoma of skin", "Eccrine Syringofibroadenoma of Mascaro", "Nevus Syringoadenomatosus Papilliferum", "Eccrine syringofibroadenomatous hyperplasia", "eccrine syringofibroadenomatous hyperplasia", "Syringofibroadenoma (morphologic abnormality)", "Eccrine syringofibroadenoma of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "syringofibroadenoma", "shortest_name_length": 19}
{"curie": "MONDO:0014411", "names": ["MYP24", "MYOPIA 24, AUTOSOMAL DOMINANT", "myopia 24, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopia 24, autosomal dominant", "shortest_name_length": 5}
{"curie": "UMLS:C1336337", "names": ["Stage IVA Esophagus Squamous Cell Carcinoma", "Stage IVA Esophageal Squamous Cell Carcinoma", "Stage IVA Squamous Cell Carcinoma of Esophagus", "Stage IVA Squamous Cell Carcinoma of the Esophagus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Esophageal Squamous Cell Carcinoma", "shortest_name_length": 43}
{"curie": "UMLS:C5419091", "names": ["Refractory Myelodysplastic/Myeloproliferative Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Myelodysplastic/Myeloproliferative Neoplasm", "shortest_name_length": 54}
{"curie": "MONDO:0000367", "names": ["teniasis", "Teniasis", "Taeniosis", "taeniasis", "Taeniasis", "Taeniases", "beef tapeworm", "Beef tapeworm", "tapeworm beef", "Taenia infection", "taenia infection", "Taenia Infection", "Taenia Infections", "Tenia infestation", "Infection, Taenia", "Taenia infestation", "Infections, Taenia", "Tenia; infestation", "infestation; Tenia", "TAENIA INFESTATION", "taeniasis saginata", "infections, Taenia", "Infection by Taenia", "infestation; Taenia", "Taenia; infestation", "Teniasis, unspecified", "taeniasis (diagnosis)", "Taeniasis, unspecified", "beef tapeworm infection", "Tenia saginata teniasis", "Beef tapeworm infection", "Infection by Taenia, NOS", "Tenia saginata infection", "beef tapeworm; infection", "Taenia saginata taeniasis", "saginata; Tenia infection", "Taenia saginata infection", "Beef tapeworm (infection)", "taenia saginata infection", "Infection caused by Taenia", "Unarmed tapeworm infection", "saginata; Taenia infection", "unarmed tapeworm infection", "Infection by Taenia saginata", "infection by taenia saginata", "taeniasis saginata (diagnosis)", "Taenia saginata infectious disease", "Taenia saginata infection (disorder)", "Infection by Taeniarhynchus saginatus", "infection by Taeniarhynchus saginatus", "Infection caused by Taenia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "taeniasis", "shortest_name_length": 8}
{"curie": "MONDO:0011096", "names": ["AGM", "autosomal agammaglobulinemia", "Autosomal agammaglobulinemia", "agammaglobulinemia, non-Bruton type", "Agammaglobulinemia, non-Bruton type", "Agammaglobulinemia, autosomal recessive", "Agammaglobulinemia due to early proB cell defect", "Agammaglobulinemia, Non-Bruton Type, Autosomal Recessive", "agammaglobulinemia, autosomal recessive, due to IGHM defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal agammaglobulinemia", "shortest_name_length": 3}
{"curie": "UMLS:C0857069", "names": ["chronic candidiasis", "Chronic candidiasis", "Chronic Candidiasis", "Candidiasis, chronic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic candidiasis", "shortest_name_length": 19}
{"curie": "MONDO:0000679", "names": ["expressive agnosia", "social emotional agnosia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "social emotional agnosia", "shortest_name_length": 18}
{"curie": "UMLS:C0220603", "names": ["Brain Neoplasm", "brain tumor pediatric", "childhood brain tumor", "Pediatric Brain Tumor", "Childhood Brain Tumor", "pediatric brain tumor", "brain tumor childhood", "brain childhood tumors", "brain tumor, pediatric", "Childhood Brain Tumors", "brain pediatric tumors", "brain tumor, childhood", "Pediatric Brain Neoplasm", "Childhood Brain Neoplasm", "Pediatric Tumor of Brain", "Childhood Tumor of Brain", "Brain tumor, child: Other", "Brain Neoplasms, Childhood", "Pediatric Neoplasm of Brain", "Childhood Neoplasm of Brain", "Pediatric Tumor of the Brain", "Childhood Tumor of the Brain", "Pediatric Neoplasm of the Brain", "Childhood Neoplasm of the Brain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Brain Neoplasm", "shortest_name_length": 14}
{"curie": "MONDO:0014100", "names": ["RCM4", "CMH22", "CMD1KK", "dilated cardiomyopathy 1KK", "MYPN dilated cardiomyopathy", "CARDIOMYOPATHY, DILATED, 1KK", "cardiomyopathy, dilated, 1KK", "dilated cardiomyopathy type 1KK", "cardiomyopathy, hypertrophic, 22", "cardiomyopathy, dilated, type 1Kk", "CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 4", "cardiomyopathy, familial restrictive, 4", "CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 22", "cardiomyopathy, familial hypertrophic, 22", "dilated cardiomyopathy caused by mutation in MYPN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dilated cardiomyopathy 1KK", "shortest_name_length": 4}
{"curie": "MONDO:0015299", "names": ["FRITSCH SYNDROME", "ASHERMAN SYNDROME", "Asherman Syndrome", "uterine synechiae", "asherman syndrome", "Asherman syndrome", "Uterine Synechiae", "Uterine synechiae", "ashermann syndrome", "Ashermans Syndrome", "Syndrome, Asherman", "ashermans syndrome", "Ashermann syndrome", "Synechiae, Uterine", "Asherman's Syndrome", "asherman's syndrome", "Asherman's syndrome", "Syndrome, Asherman's", "Amenorrhea traumatica", "AMENORRHEA TRAUMATICA", "Amenorrhoea traumatica", "Intrauterine Synechiae", "intrauterine adhesions", "intrauterine synechiae", "Synechiae, Intrauterine", "FRITSCH-ASHERMAN SYNDROME", "Asherman syndrome (disorder)", "Asherman's syndrome (diagnosis)", "Traumatic intrauterine synechiae syndrome", "TRAUMATIC INTRAUTERINE ADHESIONS OR SYNECHIAE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Asherman syndrome", "shortest_name_length": 16}
{"curie": "UMLS:C0280098", "names": ["undifferentiated carcinoma CUP", "CUP, undifferentiated carcinoma", "undifferentiated carcinoma, unknown primary", "unknown primary, undifferentiated carcinoma", "undifferentiated carcinoma of unknown primary", "Undifferentiated Carcinoma of Unknown Primary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Undifferentiated Carcinoma of Unknown Primary", "shortest_name_length": 30}
{"curie": "UMLS:C3899154", "names": ["familial testicular germ cell tumor", "Familial Testicular Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Familial Testicular Germ Cell Tumor", "shortest_name_length": 35}
{"curie": "UMLS:C5205917", "names": ["Prostate Carcinoma Metastatic in Lymph Node", "Prostate Carcinoma Metastatic in the Lymph Nodes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Carcinoma Metastatic in the Lymph Nodes", "shortest_name_length": 43}
{"curie": "MONDO:0002511", "names": ["Stenosis of lacrimal sac", "stenosis of lacrimal sac", "Stenosis of lacrimal sac (disorder)", "stenosis of lacrimal sac (diagnosis)", "Stenosis of unspecified lacrimal sac"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "stenosis of lacrimal sac", "shortest_name_length": 24}
{"curie": "MONDO:0032793", "names": ["ODLURO", "O'DONNELL-LURIA-RODAN SYNDROME", "O'Donnell-Luria-Rodan syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "O'Donnell-Luria-Rodan syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0006548", "names": ["Facial Dermatosis", "Facial Dermatoses", "facial dermatosis", "Dermatoses, Facial", "Dermatosis, Facial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "facial dermatosis", "shortest_name_length": 17}
{"curie": "MONDO:0017241", "names": ["AP4 deficiency syndrome", "AP4-related intellectual disability and spastic paraplegia", "AP4 related intellectual disability and spastic paraplegia", "severe intellectual disability and progressive spastic paraplegia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AP4-related intellectual disability and spastic paraplegia", "shortest_name_length": 23}
{"curie": "UMLS:C0020510", "names": ["Hyperplastic nodule", "Nodular hyperplasia", "hyperplastic nodule", "nodular hyperplasia", "hyperplasia nodular", "hyperplastic nodules", "Hyperplasia, nodular", "regenerative nodular hyperplasia", "nodular regenerative hyperplasia", "Nodular regenerative hyperplasia", "Hyperplasia, nodular regenerative", "Nodular hyperplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nodular hyperplasia", "shortest_name_length": 19}
{"curie": "UMLS:C3854348", "names": ["Accidental underdose"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Accidental underdose", "shortest_name_length": 20}
{"curie": "MONDO:0014597", "names": ["IMD39", "IMMUNODEFICIENCY 39", "immunodeficiency 39", "immunodeficiency type 39", "IRF7 primary immunodeficiency disease", "primary immunodeficiency disease caused by mutation in IRF7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 39", "shortest_name_length": 5}
{"curie": "MONDO:0006474", "names": ["Urothelial carcinoma", "urothelial carcinoma", "carcinomas urothelial", "transitional carcinoma", "Transitional carcinoma", "Transitional Carcinoma", "transitional cell tumor", "urothelial cell carcinoma", "transitional cell neoplasm", "carcinoma cell transitional", "Transitional Cell Carcinoma", "TRANSITIONAL CELL CARCINOMA", "CARCINOMA TRANSITIONAL CELL", "Carcinoma transitional cell", "transitional cell carcinoma", "Transitional cell carcinoma", "carcinoma of urothelial cell", "transitional cell carcinomas", "Carcinoma, Transitional Cell", "Cell Carcinoma, Transitional", "Transitional Cell Carcinomas", "Cell Carcinomas, Transitional", "Carcinomas, Transitional Cell", "Transitional cell carcinoma NOS", "Transitional cell carcinoma, NOS", "carcinoma, urothelial, malignant", "TCC - Transitional cell carcinoma", "transitional epithelial cell carcinoma", "transitional cell carcinoma (diagnosis)", "carcinoma of transitional epithelial cell", "Transitional cell carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transitional cell carcinoma", "shortest_name_length": 20}
{"curie": "MONDO:0004951", "names": ["AIDS, resistance to", "HIV1, resistance to", "AIDS, progression to", "HIV-1, resistance to", "HIV-1, RESISTANCE TO", "AIDS, PROGRESSION TO", "HIV-1, SUSCEPTIBILITY TO", "HIV-1, susceptibility to", "AIDS, slow progression to", "AIDS, rapid progression to", "HIV/AIDS, susceptibility to", "HIV infection, resistance to", "HIV1 infection, resistance to", "HIV type 1, susceptibility to", "susceptibility to HIV infection", "HIV-1 viremia, susceptibility to", "AIDS, delayed/rapid progression to", "HIV-1 disease, rapid progression of", "HIV-1 disease, delayed progression of", "rapid progression to AIDS from HIV1 infection", "acquired immunodeficiency syndrome, progression to", "human immunodeficiency virus type 1, resistance to", "ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO", "HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, RESISTANCE TO", "human immunodeficiency virus type 1, susceptibility to", "HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "susceptibility to HIV infection", "shortest_name_length": 19}
{"curie": "UMLS:C2931434", "names": ["Paraquat lung", "Paraquat induced lung disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Paraquat lung", "shortest_name_length": 13}
{"curie": "UMLS:C2748701", "names": ["Jejunal web", "Jejunal Web"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Jejunal web", "shortest_name_length": 11}
{"curie": "UMLS:C4744706", "names": ["Bladder Alveolar Soft Part Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bladder Alveolar Soft Part Sarcoma", "shortest_name_length": 34}
{"curie": "MONDO:0018277", "names": ["CMD-CRB", "CMD with cerebellar involvement", "congenital muscular dystrophy with cerebellar involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital muscular dystrophy with cerebellar involvement", "shortest_name_length": 7}
{"curie": "UMLS:C0752104", "names": ["Familial Juvenile Parkinsonism", "Parkinsonism, Familial Juvenile", "Juvenile Parkinsonism, Familial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Familial Juvenile Parkinsonism", "shortest_name_length": 30}
{"curie": "MONDO:0012499", "names": ["BUD", "BURULI ULCER, SUSCEPTIBILITY TO", "Buruli ulcer, susceptibility to", "Mycobacterium ulcerans, susceptibility to", "MYCOBACTERIUM ULCERANS, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Buruli ulcer, susceptibility to", "shortest_name_length": 3}
{"curie": "UMLS:C5555766", "names": ["Advanced HER2-Low Breast Carcinoma", "Advanced HER2 Low Breast Carcinoma", "Advanced HER2-Low Breast Adenocarcinoma", "Advanced HER2 Low Breast Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced HER2-Low Breast Carcinoma", "shortest_name_length": 34}
{"curie": "UMLS:C2111049", "names": ["Lacrimal Gland Diffuse Large B-Cell Lymphoma", "large B-cell diffuse lymphoma of lacrimal gland", "large B-cell diffuse lymphoma of lacrimal gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "large B-cell diffuse lymphoma of lacrimal gland", "shortest_name_length": 44}
{"curie": "MONDO:0016863", "names": ["Okihiro syndrome due to del(20)(q13)", "Okihiro syndrome due to monosomy 20q13", "Okihiro syndrome due to 20q13 microdeletion", "Duane-radial ray syndrome due to monosomy 20q13"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Okihiro syndrome due to 20q13 microdeletion", "shortest_name_length": 36}
{"curie": "UMLS:C0276651", "names": ["ASPERGILLOMA", "Aspergilloma", "aspergilloma", "Aspergilloma (disorder)", "aspergilloma (diagnosis)", "Intracavitary aspergillus fungus ball"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aspergilloma", "shortest_name_length": 12}
{"curie": "MONDO:0003994", "names": ["sarcoma Botryoides of the vagina", "Sarcoma Botryoides of the Vagina", "vagina botryoid rhabdomyosarcoma", "Vaginal Embryonal Rhabdomyosarcoma", "botryoid rhabdomyosarcoma of vagina", "Vaginal Botryoid-Type Embryonal Rhabdomyosarcoma", "Botryoid-Type Embryonal Rhabdomyosarcoma of the Vagina", "botryoid-type embryonal rhabdomyosarcoma of the vagina"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "botryoid-type embryonal rhabdomyosarcoma of the vagina", "shortest_name_length": 32}
{"curie": "MONDO:0018187", "names": ["genetic syndromic Pierre Robin syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "genetic syndromic Pierre Robin syndrome", "shortest_name_length": 39}
{"curie": "UMLS:C0278502", "names": ["Recurrent Stomach Cancer", "Gastric cancer recurrent", "Recurrent Gastric Cancer", "recurrent gastric cancer", "Stomach cancer recurrent", "gastric cancer, recurrent", "stomach cancer, recurrent", "Gastric carcinoma recurrent", "Recurrent Stomach Carcinoma", "Recurrent Gastric Carcinoma", "Recurrent Cancer of Stomach", "Stomach carcinoma recurrent", "Gastric Carcinoma, Recurrent", "Recurrent Carcinoma of Stomach", "Recurrent Cancer of the Stomach", "Recurrent Carcinoma of the Stomach", "Recurrent Gastric (Stomach) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "recurrent gastric cancer", "shortest_name_length": 24}
{"curie": "MONDO:0002088", "names": ["Partial Retinal Vein Occlusion", "Partial retinal vein occlusion", "partial retinal vein occlusion", "occlusion of partial retinal vein", "Partial occlusion of retinal vein", "partial occlusion of retinal vein", "partial of retinal vein occlusion", "Occlusion, partial of retinal vein", "partial retinal vein occlusion (diagnosis)", "Partial occlusion of retinal vein (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial retinal vein occlusion", "shortest_name_length": 30}
{"curie": "MONDO:0021118", "names": ["bowel neoplasm", "intestine tumor", "intestine growth", "Intestinal Tumor", "intestine tumors", "INTESTINAL TUMOR", "intestines tumor", "intestinal tumor", "Intestinal Tumors", "intestinal tumors", "growth intestines", "tumor of intestine", "intestine neoplasm", "Tumor of intestine", "Tumor of Intestines", "Intestinal Neoplasm", "Tumour of intestine", "Intestines Neoplasm", "tumor of intestines", "intestinal neoplasm", "intestinal neoplasms", "Neoplasm, Intestines", "Intestines Neoplasms", "Intestinal Neoplasms", "Neoplasm, Intestinal", "Neoplasm of intestine", "Neoplasms, Intestines", "neoplasm of intestine", "Neoplasms, Intestinal", "neoplasm of intestines", "Neoplasm of Intestines", "Tumor of the Intestines", "tumor of the intestines", "neoplasm intestinal tract", "neoplasm of the intestines", "Neoplasm of the Intestines", "intestinal benign neoplasm", "intestine neoplasm (disease)", "neoplasm of intestinal tract", "Neoplasm of intestinal tract", "Neoplasm of intestinal tract (disorder)", "Neoplasm of intestinal tract (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intestinal neoplasm", "shortest_name_length": 14}
{"curie": "MONDO:0000495", "names": ["Oppositional defiant disorder", "OPPOSITIONAL DEFIANT DISORDER", "disorder oppositional defiant", "Oppositional Defiant Disorder", "oppositional defiant disorder", "defiant disorder oppositional", "defiant disorders oppositional", "Defiant Disorder, Oppositional", "disorder; oppositional defiance", "oppositional defiance; disorder", "oppositional defiant disorder (disease)", "Oppositional defiant disorder (disorder)", "Oppositional defiant disorder (diagnosis)", "behavioral disorder; oppositional defiance", "oppositional defiant disorder of childhood", "oppositional defiance; behavioral disorder", "Attention Deficit and Disruptive Behavior Disorders", "Attention deficit and disruptive behavior disorders", "Attention deficit and disruptive behaviour disorders", "Attention Deficit and Disruptive Behavioral Disorders", "oppositional defiant disorder of childhood (diagnosis)", "Oppositional defiant disorder of childhood or adolescence", "disruptive impulse control and conduct disorder oppositional defiant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oppositional defiant disorder", "shortest_name_length": 29}
{"curie": "MONDO:0000377", "names": ["Leydig cell cancer", "cancer of Leydig cell", "Carcinoma, Leydig Cell", "Malignant Leydig cell tumor", "Malignant Leydig Cell Tumor", "malignant Leydig cell tumor", "Leydig cell tumor, malignant", "Malignant Leydig cell tumour", "LEYDIG CELL TUMOR, MALIGNANT", "Leydig cell tumour, malignant", "malignant Leydig cell neoplasm", "Malignant Leydig Cell Neoplasm", "malignant interstitial cell tumor", "Malignant interstitial cell tumor", "malignant neoplasm of Leydig cell", "Malignant Interstitial Cell Tumor", "Malignant interstitial cell tumour", "Interstitial cell tumor, malignant", "Interstitial cell tumour, malignant", "malignant interstitial cell neoplasm", "Malignant Interstitial Cell Neoplasm", "malignant Leydig cell tumor (diagnosis)", "Leydig cell tumor, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant Leydig cell tumor", "shortest_name_length": 18}
{"curie": "MONDO:0013342", "names": ["SPG48", "hereditary spastic paraplegia 48", "AP5Z1 hereditary spastic paraplegia", "hereditary spastic paraplegia type 48", "autosomal recessive spastic paraplegia 48", "spastic paraplegia 48, autosomal recessive", "SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE", "Autosomal recessive spastic paraplegia type 48", "autosomal recessive spastic paraplegia type 48", "familial spastic paraplegia autosomal recessive type 48", "Autosomal recessive spastic paraplegia type 48 (disorder)", "hereditary spastic paraplegia caused by mutation in AP5Z1", "Autosomal recessive spastic paraplegia type 48 (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hereditary spastic paraplegia 48", "shortest_name_length": 5}
{"curie": "UMLS:C0400998", "names": ["Bile duct leakage", "Bile Duct Leakage", "Bile duct leakage (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bile duct leakage", "shortest_name_length": 17}
{"curie": "MONDO:0017903", "names": ["autosomal dominant MSMD due to partial IFNgammaR2 deficiency", "autosomal dominant MSMD due to partial interferon gamma receptor 2 deficiency", "IFNGR2 autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency", "autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency", "autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 2 deficiency", "autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency caused by mutation in IFNGR2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency", "shortest_name_length": 60}
{"curie": "MONDO:0014204", "names": ["IBGC5", "BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5", "basal ganglia calcification, idiopathic, 5", "basal ganglia calcification, idiopathic, type 5"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "basal ganglia calcification, idiopathic, 5", "shortest_name_length": 5}
{"curie": "UMLS:C5420856", "names": ["Unresectable Kidney Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Kidney Carcinoma", "shortest_name_length": 29}
{"curie": "UMLS:C5668438", "names": ["Recurrent Indolent B-Cell Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Indolent B-Cell Non-Hodgkin Lymphoma", "shortest_name_length": 46}
{"curie": "UMLS:C4505456", "names": ["HIV coinfection", "HIV Coinfection", "Coinfection, HIV", "HIV Coinfections", "Coinfections, HIV"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "HIV Coinfection", "shortest_name_length": 15}
{"curie": "MONDO:0002092", "names": ["small bowel leiomyoma", "Small Bowel Leiomyoma", "leiomyoma, small Bowel", "leiomyoma, small bowel", "Leiomyoma, Small Bowel", "leiomyoma of small bowel", "Leiomyoma of Small Bowel", "Small Intestine Leiomyoma", "small intestine leiomyoma", "Leiomyoma, Small Intestine", "Small intestinal leiomyoma", "Small Intestinal Leiomyoma", "small intestinal leiomyoma", "leiomyoma, small intestine", "INTESTINE, SMALL, LEIOMYOMA", "Leiomyoma of small intestine", "Leiomyoma of Small Intestine", "leiomyoma of small intestine", "leiomyoma of the small bowel", "Leiomyoma of the Small Bowel", "leiomyoma of the small intestine", "Leiomyoma of the Small Intestine", "Leiomyoma of small intestine (disorder)", "leiomyoma of small intestine (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small intestine leiomyoma", "shortest_name_length": 21}
{"curie": "UMLS:C1336551", "names": ["T-Cell Prolymphocytic Leukemia, Cerebriform Cell Variant", "T-Cell Prolymphocytic Leukemia, Sézary Cell-like Variant", "T-Cell Prolymphocytic Leukemia, Sezary Cell-like Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-Cell Prolymphocytic Leukemia, Cerebriform Cell Variant", "shortest_name_length": 56}
{"curie": "MONDO:0013969", "names": ["COXPD11", "combined oxidative phosphorylation deficiency 11", "COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11", "combined oxidative phosphorylation defect type 11", "Combined oxidative phosphorylation defect type 11", "RMND1 combined oxidative phosphorylation deficiency", "combined oxidative phosphorylation deficiency type 11", "COXPD11 - combined oxidative phosphorylation defect type 11", "Combined oxidative phosphorylation defect type 11 (disorder)", "infantile encephaloneuromyopathy due to mitochondrial translation defect", "combined oxidative phosphorylation deficiency caused by mutation in RMND1", "ENCEPHALONEUROMYOPATHY, INFANTILE, DUE TO MITOCHONDRIAL TRANSLATION DEFECT", "Encephaloneuromyopathy, infantile, due to mitochondrial translation defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined oxidative phosphorylation defect type 11", "shortest_name_length": 7}
{"curie": "UMLS:C4526910", "names": ["Enteric adenocarcinoma", "Lung Enteric Adenocarcinoma", "Pulmonary Intestinal-Type Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lung Enteric Adenocarcinoma", "shortest_name_length": 22}
{"curie": "MONDO:0015802", "names": ["autosomal dominant mental retardation", "autosomal dominant non-syndromic mental retardation", "autosomal dominant intellectual developmental disorder", "autosomal dominant non-syndromic intellectual disability", "non-syndromic intellectual disability, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal dominant non-syndromic intellectual disability", "shortest_name_length": 37}
{"curie": "MONDO:0014865", "names": ["SCN7", "SCN 7-Autosomal Recessive", "severe congenital neutropenia 7", "Neutropenia, Severe Congenital, 7, Autosomal Recessive", "neutropenia, Severe congenital, 7, autosomal recessive", "NEUTROPENIA, SEVERE CONGENITAL, 7, AUTOSOMAL RECESSIVE", "neutropenia, severe congenital, 7, autosomal recessive", "Severe Congenital Neutropenia Type 7, Autosomal Recessive", "autosomal recessive severe congenital neutropenia due to CSF3R deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive severe congenital neutropenia due to CSF3R deficiency", "shortest_name_length": 4}
{"curie": "MONDO:0016528", "names": ["Cyllosomas", "LBWC syndrome", "Body stalk anomaly", "body stalk anomaly", "aplasia of the cord", "umbilical cord, short", "limb body wall complex", "limb-body wall complex", "Limb body wall complex", "short umbilical cord syndrome", "Limb body wall complex (disorder)", "LBWC (limb body wall complex) syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "limb body wall complex", "shortest_name_length": 10}
{"curie": "UMLS:C0280474", "names": ["Glioblastoma", "Childhood Glioblastoma", "childhood glioblastoma", "grade IV childhood astrocytoma", "astrocytoma, grade IV childhood", "pediatric anaplastic astrocytoma", "Brain tumor, child: Glioblastoma", "childhood anaplastic astrocytoma", "pediatric glioblastoma multiforme", "anaplastic astrocytoma, childhood", "childhood glioblastoma multiforme", "Pediatric Glioblastoma Multiforme", "astrocytoma, childhood anaplastic", "Childhood Glioblastoma Multiforme", "glioblastoma multiforme, childhood", "grade IV pediatric astrocytic tumor", "grade IV childhood astrocytic tumor", "grade IV pediatric astrocytic neoplasm", "grade IV childhood astrocytic neoplasm", "childhood malignant cerebral astrocytoma", "childhood high-grade cerebral astrocytoma", "CNS tumor, grade IV childhood astrocytoma", "CNS tumor, childhood grade IV astrocytoma", "pediatric cerebral astrocytoma, high-grade", "childhood cerebral astrocytoma, high-grade", "brain tumor, childhood grade IV astrocytoma", "childhood CNS tumor, glioblastoma multiforme", "CNS tumor, childhood glioblastoma multiforme", "brain tumor, childhood glioblastoma multiforme", "childhood brain tumor, glioblastoma multiforme", "high grade childhood supratentorial astrocytoma", "central nervous system tumor, astrocytoma, grade IV childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Glioblastoma", "shortest_name_length": 12}
{"curie": "UMLS:C5669672", "names": ["Post-Hepatitis Chronic Hepatopathy", "Post-Hepatitis Chronic Live Disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Post-Hepatitis Chronic Hepatopathy", "shortest_name_length": 34}
{"curie": "UMLS:C2987262", "names": ["Esophageal NEC", "Esophageal NEC G3", "Esophageal Neuroendocrine Cancer", "Esophageal Neuroendocrine Carcinoma", "Esophageal High Grade Neuroendocrine Carcinoma", "Esophageal Small and Large Cell Endocrine Carcinoma", "Esophageal Poorly Differentiated Endocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Neuroendocrine Carcinoma", "shortest_name_length": 14}
{"curie": "MONDO:0030603", "names": ["infection klebsiella", "Klebsiella infection", "Klebsiella Infection", "klebsiella infection", "Klebsiella infections", "infection, Klebsiella", "Klebsiella; infection", "Infection, Klebsiella", "Klebsiella Infections", "infection; Klebsiella", "Infections, Klebsiella", "infections, Klebsiella", "Klebsiella infection NOS", "Klebsiella infectious disease", "Klebsiella disease or disorder", "Infection caused by Klebsiella", "Klebsiella caused disease or disorder", "Infection caused by Klebsiella (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Klebsiella infectious disease", "shortest_name_length": 20}
{"curie": "EFO:0004608", "names": ["cystic fibrosis associated meconium ileus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cystic fibrosis associated meconium ileus", "shortest_name_length": 41}
{"curie": "MONDO:0001813", "names": ["Squamous blepharitis", "squamous blepharitis", "Anterior lid margin disease", "Anterior squamous lid disease", "squamous blepharitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "squamous blepharitis", "shortest_name_length": 20}
{"curie": "MONDO:0060688", "names": ["Hyperthyroxinemia due to Decreased Peripheral Conversion of T4", "HYPERTHYROXINEMIA, EUTHYROID, DUE TO DECREASED PERIPHERAL CONVERSION OF T4", "hyperthyroxinemia, euthyroid, due to decreased peripheral conversion of T4", "5-Prime-Deiodinase Deficiency, Generalized, Causing Euthyroid Hyperthyroxinemia", "HYPERTHYROXINEMIA, EUTHYROID, CAUSED BY GENERALIZED 5-PRIME-DEIODINASE DEFICIENCY", "hyperthyroxinemia, euthyroid, caused by generalized 5-prime-deiodinase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperthyroxinemia, euthyroid, caused by generalized 5-prime-deiodinase deficiency", "shortest_name_length": 62}
{"curie": "MONDO:0000282", "names": ["Whitewater Arroyo hemorrhagic fever"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Whitewater Arroyo hemorrhagic fever", "shortest_name_length": 35}
{"curie": "MONDO:0007233", "names": ["Branchioma", "Branchiomas", "Cyst;branchial", "Branchial cyst", "Branchial Cyst", "branchial cyst", "branchial cysts", "BRANCHIAL CYSTS", "Branchial Cysts", "Branchial cleft", "Cyst, Branchial", "branchial cleft", "Branchial Cleft", "Branchial cysts", "Cysts, Branchial", "branchial clefting", "Branchial Cleft Cyst", "Branchial cleft, NOS", "Branchial cleft cyst", "cyst branchial cleft", "branchial cleft cyst", "BRANCHIAL CLEFT CYST", "Cyst, Branchial Cleft", "Cleft Cyst, Branchial", "branchial cleft; cyst", "cyst; branchial cleft", "Branchial cleft cysts", "branchial cleft cysts", "Branchial Cleft Cysts", "Cleft Cysts, Branchial", "Cysts, Branchial Cleft", "Branchial cleft anomaly", "Cyst of Branchial Cleft", "Branchial Cleft Remnant", "branchial cleft remnant", "Cyst of branchial cleft", "branchial cleft anomalies", "BRANCHIAL CLEFT ANOMALIES", "Branchial Cleft Anomalies", "branchial cyst (diagnosis)", "second branchial cleft cyst", "Type 2 branchial cleft cyst", "Cyst of the Branchial Cleft", "Second branchial cleft cyst", "branchial cleft malformations", "Second branchial cleft fistula", "second branchial cleft fistula", "Second branchial cleft anomaly", "second branchial cleft anomaly", "Branchial cleft cyst (disorder)", "Branchial cleft malformation NOS", "Branchial cleft anomaly (disorder)", "Remnant of embryonic branchial cleft", "Second branchial cleft cyst (disorder)", "Branchial cyst (morphologic abnormality)", "branchial cleft malformations (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "second branchial cleft anomaly", "shortest_name_length": 10}
{"curie": "UMLS:C0086241", "names": ["Tonic seizure", "Tonic Epilepsy", "Epilepsy, Tonic", "epilepsy; tonic", "tonic; epileptic", "Tonic Epilepsies", "Epilepsies, Tonic", "Tonic epileptic seizure", "Epileptic seizures, tonic", "Tonic epileptic seizure (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epilepsy, Tonic", "shortest_name_length": 13}
{"curie": "MONDO:0006325", "names": ["OM", "Eye Melanoma", "eye melanoma", "eye; melanoma", "melanoma; eye", "melanoma of eye", "Melanoma of eye", "Ocular Melanoma", "Ocular melanoma", "Melanoma of Eye", "ocular melanoma", "melanoma, ocular", "Ocular melanomas", "melanoma of eyeball", "melanoma of the eye", "Melanoma of the Eye", "intraocular melanoma", "malignant melanoma eye", "eye malignant melanoma", "eye melanoma (disease)", "malignant melanoma of eye", "Malignant melanoma of eye", "Melanoma of eye (disorder)", "MM (malignant melanoma) of eye", "melanoma of eyeball (diagnosis)", "eyeball of camera-type eye melanoma", "Malignant melanoma of eye (disorder)", "malignant melanoma of eye (diagnosis)", "eyeball of camera-type eye melanoma (disease)", "melanoma (disease) of eyeball of camera-type eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ocular melanoma", "shortest_name_length": 2}
{"curie": "UMLS:C3267156", "names": ["Operative bleeding"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Operative bleeding", "shortest_name_length": 18}
{"curie": "UMLS:C0521587", "names": ["Gastrointestinal stenosis", "Gastrointestinal Stenosis", "Digestive System Stenosis", "GI TRACT STENOSIS ANY SITE", "GI tract stenosis any site", "Gastrointestinal stenosis NOS", "Gastrointestinal stenosis, NOS", "Gastrointestinal System Stenosis", "Gastrointestinal stenosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastrointestinal stenosis", "shortest_name_length": 25}
{"curie": "UMLS:C2981668", "names": ["stage III distal bile duct cancer", "Stage III Distal Bile Duct Cancer", "stage III distal bile duct cancer AJCC v7", "Stage III Distal Bile Duct Cancer AJCC v7", "stage III distal extrahepatic bile duct cancer", "Stage III Extrahepatic (Distal) Bile Duct Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Distal Bile Duct Cancer AJCC v7", "shortest_name_length": 33}
{"curie": "UMLS:C5557147", "names": ["Cervical Cancer by AJCC v9 Stage", "Cervical Carcinoma by AJCC v9 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cervical Cancer by AJCC v9 Stage", "shortest_name_length": 32}
{"curie": "MONDO:0013820", "names": ["CSS3", "MRD15", "COFFIN-SIRIS SYNDROME 3", "Coffin-Siris syndrome 3", "COFFIN-SIRIS syndrome 3", "SMARCB1-related BAFopathy", "SMARCB1 Coffin-Siris syndrome", "autosomal dominant mental retardation 15", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 15", "mental retardation, autosomal dominant 15", "autosomal dominant intellectual disability 15", "intellectual disability, autosomal dominant 15", "mental retardation, autosomal dominant type 15", "intellectual disability, autosomal dominant type 15", "Coffin-Siris syndrome caused by mutation in SMARCB1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 15", "shortest_name_length": 4}
{"curie": "UMLS:C4526715", "names": ["Stage IA2 Lung Cancer", "Stage IA2 Lung Cancer AJCC v8", "stage IA2 lung cancer AJCC v8", "stage IA2 non-small cell lung cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IA2 Lung Cancer AJCC v8", "shortest_name_length": 21}
{"curie": "UMLS:C3272800", "names": ["MVHP", "Colorectal MVHP", "Colorectal Microvesicular Hyperplastic Polyp"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Colorectal Microvesicular Hyperplastic Polyp", "shortest_name_length": 4}
{"curie": "UMLS:C5446514", "names": ["Conjunctival Mucosa-Associated Lymphoid Tissue Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conjunctival Mucosa-Associated Lymphoid Tissue Lymphoma", "shortest_name_length": 55}
{"curie": "MONDO:0023124", "names": ["familial PAH, leucopenia and ASD", "familial pulmonary arterial hypertension, leucopenia and ASD", "familial pulmonary arterial hypertension leucopenia and atrial septal defect"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial pulmonary arterial hypertension leucopenia and atrial septal defect", "shortest_name_length": 32}
{"curie": "MONDO:0024295", "names": ["bacterial skin disease", "disease, bacterial skin", "skin disease, bacterial", "bacterial skin diseases", "diseases, bacterial skin", "Skin Diseases, Bacterial", "Bacteria skin disease caused by infection", "skin disease caused by bacterial infection", "Bacteria caused skin disease caused by infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin disease caused by bacterial infection", "shortest_name_length": 22}
{"curie": "MONDO:0002683", "names": ["Choroid Plexus Neoplasm", "choroid plexus neoplasm", "Adult Choroid Plexus Tumor", "adult choroid plexus tumor", "choroid plexus tumor, adult", "tumor, adult choroid plexus", "adult choroid plexus cancer", "Adult Choroid Plexus Neoplasm", "adult choroid plexus neoplasm", "tumor of adult choroid plexus", "Tumor of Adult Choroid Plexus", "neoplasm of adult choroid plexus", "Neoplasm of Adult Choroid Plexus", "choroid plexus neoplasm of adults", "tumor of the adult choroid plexus", "Tumor of the Adult Choroid Plexus", "neoplasm of the adult choroid plexus", "Neoplasm of the Adult Choroid Plexus", "neoplasm of the adult Choroid Plexus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "adult choroid plexus neoplasm", "shortest_name_length": 23}
{"curie": "MONDO:0020713", "names": ["PVOD", "PVOD1", "pulmonary venoocclusive disease 1", "PULMONARY VENOOCCLUSIVE DISEASE 1, AUTOSOMAL DOMINANT", "pulmonary venoocclusive disease 1, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary venoocclusive disease 1", "shortest_name_length": 4}
{"curie": "UMLS:C4727364", "names": ["Recurrent Anal Mucinous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Anal Mucinous Adenocarcinoma", "shortest_name_length": 38}
{"curie": "UMLS:C1336159", "names": ["stage IIA esophageal cancer", "Stage IIA Esophageal Cancer", "esophageal cancer stage IIA", "Esophageal Cancer Stage IIA", "Stage IIA Esophagus Carcinoma", "stage IIA esophageal carcinoma", "Stage IIA Esophageal Carcinoma", "Stage IIA Carcinoma of Esophagus", "stage IIA carcinoma of esophagus", "Stage IIA Esophageal Cancer AJCC v7", "stage IIA esophageal cancer AJCC v7", "Stage IIA Carcinoma of the Esophagus", "stage IIA carcinoma of the esophagus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Esophagus Carcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0013204", "names": ["FECD4", "SLC4A11 Fuchs' endothelial dystrophy", "CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 4", "corneal dystrophy, Fuchs endothelial, 4", "Corneal Dystrophy, Fuchs Endothelial, 4", "corneal dystrophy, Fuchs endothelial, type 4", "CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, LATE-ONSET", "corneal dystrophy, Fuchs endothelial, late-onset", "Fuchs' endothelial dystrophy caused by mutation in SLC4A11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal dystrophy, Fuchs endothelial, 4", "shortest_name_length": 5}
{"curie": "MONDO:0010818", "names": ["RP12", "RP 12", "retinitis pigmentosa 12", "RETINITIS PIGMENTOSA 12", "Retinitis Pigmentosa 12", "retinitis pigmentosa-12", "RP WITH OR WITHOUT PPRPE", "RP with or without Pprpe", "CRB1 retinitis pigmentosa", "retinitis pigmentosa type 12", "retinitis pigmentosa caused by mutation in CRB1", "RP with or without preserved Paraarteriole retinal pigment epithelium", "RP WITH OR WITHOUT PRESERVED PARAARTERIOLE RETINAL PIGMENT EPITHELIUM", "retinitis pigmentosa with or without Paraarteriolar preservation of retinal pigment epithelium", "RETINITIS PIGMENTOSA WITH OR WITHOUT PARAARTERIOLAR PRESERVATION OF RETINAL PIGMENT EPITHELIUM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 12", "shortest_name_length": 4}
{"curie": "MONDO:0007908", "names": ["MSL", "Lipomatosis", "Madelung Neck", "Madelung neck", "Madelungs Neck", "Madelung's Neck", "Madelung's neck", "Launois-Bensaude", "Madelung disease", "Madelung Disease", "Madelungs Disease", "Disease, Madelung", "Madelung's Disease", "madelung's disease", "Madelung's disease", "disease madelung s", "Disease, Madelung's", "symmetrical lipomatosis", "Symmetrical lipomatosis", "Lipomatosis, symmetrical", "Launois-Bensaude Syndrome", "Launois Bensaude Syndrome", "Launois-Bensaude syndrome", "Launois Bensaude lipomatosis", "Launois-Bensaude lipomatosis", "Benign symmetric lipomatosis", "Cephalothoracic Lipodystrophy", "lipomatosis; Launois-Bensaude", "Launois-Bensaude; lipomatosis", "cephalothoracic lipodystrophy", "Cephalothoracic lipodystrophy", "Launois-Bensaude's lipomatosis", "Lipodystrophy, Cephalothoracic", "lipodystrophy, cephalothoracic", "Multiple Symmetric Lipomatosis", "LIPODYSTROPHY, CEPHALOTHORACIC", "benign symmetrical lipomatosis", "Benign Symmetrical Lipomatosis", "Multiple Symmetric Lipomatoses", "Benign Symmetrical Lipomatoses", "multiple symmetric lipomatosis", "Multiple symmetric lipomatosis", "familial symmetric lipomatosis", "lipomatosis, multiple symmetric", "Symmetrical Lipomatosis, Benign", "Symmetric Lipomatosis, Multiple", "LIPOMATOSIS, MULTIPLE SYMMETRIC", "Symmetric Lipomatoses, Multiple", "Lipomatosis, Multiple Symmetric", "Cephalothoracic Lipodystrophies", "Lipomatosis, Benign Symmetrical", "Lipomatoses, Multiple Symmetric", "Lipodystrophies, Cephalothoracic", "cervical Symmetrical Lipomatosis", "Multiple Symmetrical Lipomatoses", "cervical symmetrical lipomatosis", "Multiple Symmetrical Lipomatosis", "multiple symmetrical lipomatosis", "Multiple symmetrical lipomatosis", "Cervical Symmetrical Lipomatosis", "Symmetrical Lipomatosis, Multiple", "Lipomatosis, Multiple Symmetrical", "Nodular Circumscribed Lipomatoses", "Nodular Circumscribed Lipomatosis", "Symmetrical Lipomatoses, Multiple", "Nodular circumscribed lipomatosis", "Circumscribed Lipomatosis, Nodular", "Circumscribed Lipomatoses, Nodular", "Lipomatosis, Nodular Circumscribed", "Lipomatosis, nodular circumscribed", "Lipomatoses, Nodular Circumscribed", "Familial benign cervical lipomatosis", "Lipomatosis Familial Benign Cervical", "familial benign cervical lipomatosis", "LIPOMATOSIS, FAMILIAL BENIGN CERVICAL", "Lipomatosis, Familial Benign Cervical", "lipomatosis, familial benign cervical", "LMS - Multiple symmetrical lipomatosis", "Launois-Bensaude lipomatosis (diagnosis)", "Benign symmetrical lipomatosis of Madelung", "Multiple symmetrical lipomatosis (disorder)", "Nodular circumscribed lipomatosis (disorder)", "lipoid metabolism disorder Launois-Bensaude lipomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple symmetric lipomatosis", "shortest_name_length": 3}
{"curie": "MONDO:0021577", "names": ["malignant neuroma of mediastinum", "Malignant neuroma of mediastinum", "malignant mediastinal neural neoplasm", "mediastinal neoplasm malignant neuroma", "Malignant neuroma of mediastinum (disorder)", "malignant neuroma of mediastinum (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant mediastinal neural neoplasm", "shortest_name_length": 32}
{"curie": "MONDO:0002853", "names": ["rectum rhabdomyosarcoma", "Rectal Rhabdomyosarcoma", "rectal rhabdomyosarcoma", "rhabdomyosarcoma of rectum", "Rhabdomyosarcoma of rectum", "Rhabdomyosarcoma of Rectum", "Rhabdomyosarcoma of the Rectum", "rhabdomyosarcoma of the rectum", "rectum rhabdomyosarcoma (disease)", "rhabdomyosarcoma (disease) of rectum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "rectum rhabdomyosarcoma", "shortest_name_length": 23}
{"curie": "MONDO:0001673", "names": ["Diarrhea", "The runs", "DIARRHEA", "diarrhea", "diarrhoea", "Diarrheas", "diarrheas", "The trots", "DIARRHOEA", "Diarrhoea", "watery stool", "Loose Stools", "D - Diarrhea", "loose stools", "Watery stool", "LOOSE STOOLS", "STOOLS LOOSE", "Diarrhea NOS", "RNDx diarrhea", "D - Diarrhoea", "Watery stools", "Diarrhoea NOS", "watery stools", "Diarrhea, NOS", "runs(diarrhea)", "runs(diarrhoea)", "frequent stools", "Runs(diarrhoea)", "Frequent Stools", "diarrhea running", "Diarrhea symptom", "Diarrheal Disease", "Diarrhoea symptom", "Diarrhea disorder", "diarrheal disease", "Diarrheal disease", "diarrhea symptoms", "symptoms diarrhea", "Diarrheal disorder", "Diarrhoeal disease", "Lienteric diarrhea", "diarrhoea symptoms", "Diarrhea (finding)", "Diarrhoea disorder", "diarrhoeal disease", "diarrheal disorder", "loose bowel motion", "diarrhea (symptom)", "diarrheal diseases", "Diarrhoeal disorder", "Loose bowel motions", "diarrhoeal diseases", "Lienteric diarrhoea", "loose bowel movement", "Loose bowel movement", "bowels loose movement", "Diarrhea, unspecified", "bowel loose movements", "Diarrheal disease, NOS", "Observation of diarrhea", "Diarrhoeal disease, NOS", "Observation of diarrhoea", "RNDx diarrhea (diagnosis)", "Diarrhea symptom (finding)", "intestinal disorder diarrheal", "Diarrheal disorder (disorder)", "Diarrheal disorder (diagnosis)", "diarrhea of presumed infectious origin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diarrheal disease", "shortest_name_length": 8}
{"curie": "UMLS:C4520917", "names": ["Stage IIA Soft Tissue Sarcoma", "Stage IIA Adult Sarcoma of Soft Tissue", "Stage IIA Adult Sarcoma of the Soft Tissue", "Stage IIA Adult Soft Tissue Sarcoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Adult Soft Tissue Sarcoma AJCC v7", "shortest_name_length": 29}
{"curie": "MONDO:0018899", "names": ["PCA", "Benson syndrome", "Benson's syndrome", "Posterior cortical atrophy", "posterior cortical atrophy", "Biparietal Alzheimer disease", "biparietal Alzheimer disease", "Posterior cortical atrophy syndrome", "Posterior cortical atrophy syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "posterior cortical atrophy", "shortest_name_length": 3}
{"curie": "MONDO:0020813", "names": ["benign sertoli cell tumor of testis", "Benign Sertoli Cell Tumor of Testis", "benign testicular sertoli cell tumor", "Benign Testicular Sertoli Cell Tumor", "Benign Sertoli Cell Neoplasm of Testis", "benign sertoli cell neoplasm of testis", "Benign Sertoli Cell Tumor of the Testis", "benign sertoli cell tumor of the testis", "benign testicular sertoli cell neoplasm", "Benign Testicular Sertoli Cell Neoplasm", "Benign Sertoli Cell Neoplasm of the Testis", "benign sertoli cell neoplasm of the testis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign testicular sertoli cell tumor", "shortest_name_length": 35}
{"curie": "UMLS:C1269955", "names": ["Invasion", "Tumor invasion", "Tumor Invasion", "Tumour invasion", "Tumor Cell Invasion", "Local Tumor Invasion"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Tumor Cell Invasion", "shortest_name_length": 8}
{"curie": "MONDO:0013400", "names": ["P450scc Deficiency", "p450scc deficiency", "P450scc DEFICIENCY", "XY sex reversal-adrenal failure", "congenital adrenal insufficiency", "Adrenal Insufficiency, Congenital", "XY sex reversal-adrenal failure syndrome", "cholesterol side-chain cleavage deficiency", "Cholesterol Side-Chain Cleavage Deficiency", "Adrenal insufficiency, congenital, with 46,XY sex reversal", "adrenal insufficiency, congenital, with 46XY sex reversal, partial or complete", "adrenal insufficiency, congenital, with 46,XY SEX reversal, partial or complete", "ADRENAL INSUFFICIENCY, CONGENITAL, WITH 46,XY SEX REVERSAL, PARTIAL OR COMPLETE", "46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency", "46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency syndrome", "Congenital adrenal insuffiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital adrenal insuffiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency", "shortest_name_length": 18}
{"curie": "MONDO:0005105", "names": ["Melanoma", "MELANOMA", "melanoma", "Melanomas", "melanomas", "Melanoma, NOS", "Nevocarcinoma", "Melanosarcoma", "nevocarcinoma", "melanosarcoma", "Naevocarcinoma", "melanocarcinoma", "Melanocarcinoma", "Melanoma syndrome", "melanoma syndrome", "malignant melanoma", "melanoma (disease)", "melanoma malignant", "cutaneous melanoma", "MALIGNANT MELANOMA", "Malignant melanoma", "Melanoma malignant", "MELANOMA MALIGNANT", "Malignant Melanoma", "Malignant Melanomas", "Melanoma, Malignant", "malignant melanomas", "melanoma, malignant", "MELANOMA, MALIGNANT", "Melanomas, Malignant", "Skin cancer (melanoma)", "Malignant melanoma NOS", "Malignant melanoma, NOS", "MM - Malignant melanoma", "MM - malignant melanoma", "malignant neoplasm melanoma", "Cancer of skin pigment cells", "Malignant melanoma (disorder)", "malignant melanoma (diagnosis)", "Malignant melanoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melanoma", "shortest_name_length": 8}
{"curie": "MONDO:0010016", "names": ["SOST", "SOST1", "sclerosteosis 1", "SCLEROSTEOSIS 1", "SOST sclerosteosis", "sclerosteosis type 1", "cortical hyperostosis with syndactyly", "sclerosteosis caused by mutation in SOST"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sclerosteosis 1", "shortest_name_length": 4}
{"curie": "UMLS:C3640019", "names": ["D-Transposition of the Great Vessels with Intact Ventricular Septum", "Dextro-Transposition of the Great Vessels with Intact Ventricular Septum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dextro-Transposition of the Great Vessels with Intact Ventricular Septum", "shortest_name_length": 67}
{"curie": "MONDO:0013215", "names": ["DFNB79", "autosomal recessive deafness 79", "Deafness, Autosomal Recessive 79", "DEAFNESS, AUTOSOMAL RECESSIVE 79", "deafness, autosomal recessive 79", "deafness, autosomal recessive type 79", "autosomal recessive nonsyndromic deafness 79", "TPRN autosomal recessive nonsyndromic deafness", "autosomal recessive nonsyndromic hearing loss 79", "autosomal recessive nonsyndromic deafness type 79", "autosomal recessive nonsyndromic deafness caused by mutation in TPRN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 79", "shortest_name_length": 6}
{"curie": "UMLS:C0345535", "names": ["Lower Gum Carcinoma", "Carcinoma of lower gum", "Carcinoma of Lower Gum", "Lower Gingival Carcinoma", "Carcinoma of Lower Gingiva", "Carcinoma of the Lower Gum", "Carcinoma of the Lower Gingiva", "Carcinoma of lower gum (disorder)", "Carcinoma of lower gum (diagnosis)", "gum neoplasm malignant carcinoma of lower gum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Carcinoma of lower gum", "shortest_name_length": 19}
{"curie": "UMLS:C1096543", "names": ["superficial punctate keratopathy", "Superficial punctate keratopathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Superficial punctate keratopathy", "shortest_name_length": 32}
{"curie": "MONDO:0019646", "names": ["unilateral congenital megacalycosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "unilateral congenital megacalycosis", "shortest_name_length": 35}
{"curie": "UMLS:C0278561", "names": ["esophageal cancer stage III", "esophagus cancer, stage III", "stage III esophageal cancer", "Stage III Esophageal Cancer", "esophageal cancer, stage III", "stage III cancer of the esophagus", "Esophageal Cancer Stage III AJCC v6", "Stage III Esophageal Cancer AJCC v6", "Stage III Esophagus Carcinoma AJCC v6", "Stage III Esophageal Carcinoma AJCC v6", "Stage III Carcinoma of Esophagus AJCC v6", "Stage III Carcinoma of the Esophagus AJCC v6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Esophageal Cancer", "shortest_name_length": 27}
{"curie": "MONDO:0003332", "names": ["Malignant struma ovarii", "malignant struma ovarii", "Malignant Struma Ovarii", "struma ovarii, malignant", "Struma ovarii, malignant", "struma; ovarii, malignant", "malignant struma ovarii (diagnosis)", "Thyroid Carcinoma Arising in Struma Ovarii", "struma ovarii, malignant (morphologic abnormality)", "Struma ovarii, malignant (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant struma ovarii", "shortest_name_length": 23}
{"curie": "MONDO:0021290", "names": ["Stage 0 Appendix Cancer", "stage 0 appendix cancer", "stage 0 appendix carcinoma", "Stage 0 Appendix Carcinoma", "Carcinoma in situ of Appendix", "carcinoma in situ of appendix", "Carcinoma in situ of appendix", "appendiceal carcinoma in situ", "carcinoma in situ of the appendix", "Carcinoma in situ of the Appendix", "Stage 0 Appendix Carcinoma AJCC v7", "stage 0 appendix carcinoma aJCC v7", "vermiform appendix carcinoma in situ", "stage 0 vermiform appendix carcinoma", "vermiform appendix in situ carcinoma", "carcinoma in situ of vermiform appendix", "Carcinoma in situ of appendix (disorder)", "carcinoma in situ of appendix (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma in situ of appendix", "shortest_name_length": 23}
{"curie": "MONDO:0018866", "names": ["AGS", "CREE ENCEPHALITIS", "Cree Encephalitis", "Cree encephalitis", "AICARDI-GOUTIERES SYNDROME", "Aicardi-Goutières syndrome", "Aicardi-Goutieres syndrome", "aicardi goutieres syndrome", "Aicardi Goutieres syndrome", "Pseudotoxoplasmosis syndrome", "PSEUDOTOXOPLASMOSIS SYNDROME", "pseudotoxoplasmosis syndrome", "Aicardi Goutieres syndrome (disorder)", "Aicardi Goutieres syndrome (diagnosis)", "microcephaly-chorioretinopathy syndrome", "Encephalopathy with basal ganglia calcification", "Encephalopathy with Basal Ganglia Calcification", "encephalopathy with basal ganglia calcification", "Encephalopathy with intracranial calcification and chronic lymphocytosis of cerebrospinal fluid", "encephalopathy with intracranial calcification and chronic lymphocytosis of cerebrospinal fluid", "Familial Infantile Encephalopathy with Intracranial Calcification and Chronic Cerebrospinal Fluid Lymphocytosis", "ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATION AND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS", "encephalopathy, familial infantile, with calcification of basal ganglia and chronic cerebrospinal fluid lymphocytosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Aicardi-Goutieres syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C3899653", "names": ["Malignant Childhood Penile Neoplasm", "Childhood Malignant Penile Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Malignant Penile Neoplasm", "shortest_name_length": 35}
{"curie": "MONDO:0016268", "names": ["endometrial capillary carcinoma", "body of uterus papillary carcinoma", "papillary carcinoma of the corpus uteri"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "papillary carcinoma of the corpus uteri", "shortest_name_length": 31}
{"curie": "MONDO:0010871", "names": ["succinic acidemia", "SUCCINIC ACIDEMIA", "Succinic Acidemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "succinic acidemia", "shortest_name_length": 17}
{"curie": "UMLS:C0015409", "names": ["Eye penetration", "Ocular penetration", "Penetrating Eye Injury", "Penetrating eye injury", "penetrating eye injury", "Ocular penetration NOS", "eye injury penetrating", "Injury, Penetrating Eye", "Ocular penetration, NOS", "Penetration of eye, NOS", "Eye Injury, Penetrating", "penetrating eye injuries", "Penetrating wound of eye", "Penetrating Eye Injuries", "eye injuries penetrating", "Eye Injuries, Penetrating", "Injuries, Penetrating Eye", "eyeball; penetrating wound", "penetrating wound; eyeball", "injury; eyeball, penetrating", "penetrating wound of eyeball", "eyeball; injury, penetrating", "penetrating injury of eyeball", "Unspecified ocular penetration", "open wound of eyeball penetrating", "Penetrating wound of eyeball, NOS", "Penetrating wound of eye (disorder)", "eye trauma penetrating injury of eyeball", "penetrating wound of eyeball (diagnosis)", "penetrating injury of eyeball (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eye Injuries, Penetrating", "shortest_name_length": 15}
{"curie": "MONDO:0007104", "names": ["PDALS", "G-PDC", "ALS-PDC", "ALS-pDC", "GUAM DISEASE", "Guam Disease", "Guam disease", "Disease, Guam", "Lytico Bodig disease", "Lytico-Bodig disease", "Lytigo-Bodig disease", "parkinsonism-dementia-ALS complex", "Parkinsonism-dementia-ALS complex", "Parkinson-dementia complex of Guam", "Guam parkinsonism-dementia complex", "Parkinson dementia complex of Guam", "ALS-parkinsonism dementia complex 1", "Amyotrophic Lateral Sclerosis, Guam Form", "Amyotrophic lateral sclerosis, Guam form", "Guam Form of Amyotrophic Lateral Sclerosis", "Parkinson's disease - dementia complex on Guam", "ALS-parkinsonism dementia complex 1 (diagnosis)", "amyotrophic lateral sclerosis-parkinsonism-dementia complex", "AMYOTROPHIC LATERAL SCLEROSIS-PARKINSONISM/DEMENTIA COMPLEX 1", "amyotrophic lateral sclerosis-parkinsonism/dementia complex 1", "Amyotrophic Lateral Sclerosis Parkinsonism Dementia Complex 1", "Amyotrophic lateral sclerosis, parkinsonism, dementia complex", "amyotrophic lateral sclerosis-PARKINSONISM/dementia complex 1", "Amyotrophic Lateral Sclerosis-Parkinsonism-Dementia Complex 1", "amyotrophic lateral sclerosis-Parkinsonism/dementia Complex type 1", "amyotrophic lateral sclerosis-parkinsonism/dementia complex of Guam", "amyotrophic lateral sclerosis-Parkinsonism/dementia Complex of Guam", "AMYOTROPHIC LATERAL SCLEROSIS-PARKINSONISM/DEMENTIA COMPLEX OF GUAM", "amyotrophic lateral sclerosis, Parkinsonism/dementia complex of Guam", "Amyotrophic Lateral Sclerosis, Parkinsonism Dementia Complex of Guam", "Amyotrophic lateral sclerosis-parkinsonism-dementia of Guam syndrome", "amyotrophic lateral sclerosis-parkinsonism-dementia of Guam syndrome", "Amyotrophic Lateral Sclerosis, Parkinsonism-Dementia Complex of Guam", "PDALS (parkinsonism, dementia, amyotrophic lateral sclerosis) complex", "Amyotrophic lateral sclerosis, parkinsonism, dementia of Guam syndrome", "Amyotrophic lateral sclerosis, parkinsonism, dementia complex (disorder)", "amyotrophic lateral sclerosis-parkinsonism/dementia complex, susceptibility to"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyotrophic lateral sclerosis-parkinsonism-dementia complex", "shortest_name_length": 5}
{"curie": "UMLS:C4744723", "names": ["Locally Advanced Cervical Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Advanced Cervical Carcinoma", "shortest_name_length": 35}
{"curie": "MONDO:0013772", "names": ["CCHLND", "congenital cataracts, hearing loss, and neurodegeneration", "CONGENITAL CATARACTS, HEARING LOSS, AND NEURODEGENERATION", "congenital cataract-deafness-severe developmental delay syndrome", "lethal neurodegenerative disorder due to copper transport defect", "congenital cataract-hearing loss-severe developmental delay syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital cataract-hearing loss-severe developmental delay syndrome", "shortest_name_length": 6}
{"curie": "MONDO:0009856", "names": ["PTRPLS", "Peters-Plus Syndrome", "peters plus syndrome", "Peters Plus Syndrome", "Peters plus syndrome", "Peters-plus syndrome", "PETERS-PLUS SYNDROME", "Peters'-Plus Syndrome", "Peters' Plus Syndrome", "krause-kivlin syndrome", "KRAUSE-KIVLIN SYNDROME", "Krause-Kivlin syndrome", "Peters plus syndrome (disorder)", "Krause-van Schooneveld-Kivlin syndrome", "Krause-Van Schooneveld-Kivlin Syndrome", "Peters anomaly with short-limb dwarfism", "Peters anomaly with short limb dwarfism", "PETERS ANOMALY WITH SHORT-LIMB DWARFISM", "Peters Anomaly With Short-Limb Dwarfism", "Peters Anomaly-Short Limb Dwarfism Syndrome", "Peters anomaly-short limb dwarfism syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Peters plus syndrome", "shortest_name_length": 6}
{"curie": "UMLS:C5556495", "names": ["Localized Muscle Invasive Bladder Urothelial Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Localized Muscle Invasive Bladder Urothelial Carcinoma", "shortest_name_length": 54}
{"curie": "UMLS:C0853008", "names": ["Parkinson's disease aggravated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parkinson's disease aggravated", "shortest_name_length": 30}
{"curie": "MONDO:0005253", "names": ["High Output Heart Failure", "high output heart failure", "High output heart failure", "HEART FAILURE, HIGH OUTPUT", "Heart failure, high output", "cardiac failure high output", "high output cardiac failure", "Cardiac failure high output", "high cardiac output failure", "High output heart failure (disorder)", "High output heart failure (diagnosis)", "HYPERKINETIC HEART SYNDROME, WITH FAILURE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "high output heart failure", "shortest_name_length": 25}
{"curie": "UMLS:C0241950", "names": ["bowel infarction", "Bowel infarction", "bowel; infarction", "infarction; bowel", "Intestinal infarct", "infarcts intestinal", "infarction; intestine", "intestinal infarction", "Intestinal infarction", "intestine; infarction", "INTESTINAL INFARCTION"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intestinal infarction", "shortest_name_length": 16}
{"curie": "UMLS:C1112251", "names": ["Feeding Tube Complication", "feeding tube complication", "Feeding tube complication", "complications feeding tube"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Feeding tube complication", "shortest_name_length": 25}
{"curie": "UMLS:C5205056", "names": ["Recurrent High-Grade B-Cell Lymphoma", "Recurrent High Grade B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent High Grade B-Cell Lymphoma", "shortest_name_length": 36}
{"curie": "MONDO:0012829", "names": ["IBD12", "inflammatory bowel disease 12", "INFLAMMATORY BOWEL DISEASE 12", "Inflammatory Bowel Disease 12", "inflammatory bowel disease type 12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inflammatory bowel disease 12", "shortest_name_length": 5}
{"curie": "MONDO:0021525", "names": ["benign corpus uteri tumor", "Benign Corpus Uteri Tumor", "Benign Uterine Body Tumor", "benign uterine body tumor", "benign uterine corpus tumor", "Benign Uterine Corpus Tumor", "benign corpus uteri neoplasm", "Benign Uterine Body Neoplasm", "Benign Tumor of Corpus Uteri", "benign uterine body neoplasm", "Benign Tumor of Uterine Body", "Benign Corpus Uteri Neoplasm", "benign tumor of corpus uteri", "benign tumor of uterine body", "Benign Tumor of Body of Uterus", "Benign Uterine Corpus Neoplasm", "Benign Tumor of Uterine Corpus", "benign tumor of uterine corpus", "benign tumor of body of uterus", "benign uterine corpus neoplasm", "body of uterus benign neoplasm", "Benign neoplasm of corpus uteri", "Benign Neoplasm of Uterine Body", "Benign Neoplasm of Corpus Uteri", "benign neoplasm of uterine body", "benign neoplasm of corpus uteri", "benign tumor of the corpus uteri", "benign tumor of the uterine body", "Benign Tumor of the Corpus Uteri", "Benign Tumor of the Uterine Body", "Benign Neoplasm of Body of Uterus", "Benign Neoplasm of Uterine Corpus", "benign neoplasm of uterine corpus", "benign neoplasm of body of uterus", "Benign neoplasm of body of uterus", "Benign Tumor of the Uterine Corpus", "benign tumor of the uterine corpus", "benign tumor of the body of uterus", "Benign Tumor of the Body of Uterus", "Benign Neoplasm of the Uterine Body", "benign neoplasm of the corpus uteri", "benign neoplasm of the uterine body", "Benign Neoplasm of the Corpus Uteri", "Benign Neoplasm of the Uterine Corpus", "Benign Neoplasm of the Body of Uterus", "benign neoplasm of the body of uterus", "benign neoplasm of the uterine corpus", "Benign neoplasm of body of uterus (disorder)", "benign neoplasm of body of uterus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of corpus uteri", "shortest_name_length": 25}
{"curie": "MONDO:0002737", "names": ["Acute sanguinous otitis media", "acute sanguinous otitis media", "acute sanguineous otitis media", "otitis; media, acute, sanguineous", "Acute sanguinous otitis media (disorder)", "acute sanguineous otitis media (diagnosis)", "Acute non-suppurative otitis media - bloody", "Acute non-suppurative otitis media - sanguinous", "Acute non-suppurative otitis media with hemotympanum", "Acute non-suppurative otitis media with haemotympanum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute sanguinous otitis media", "shortest_name_length": 29}
{"curie": "OMIM:612630", "names": ["HRM1", "HAIR MORPHOLOGY 1", "HAIR THICKNESS, VARIATION IN"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 4}
{"curie": "EFO:0010143", "names": ["chronic mountain sickness"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic mountain sickness", "shortest_name_length": 25}
{"curie": "MONDO:0001110", "names": ["pyelonephritis chronic", "chronic pyelonephritis", "Chronic pyelonephritis", "Pyelonephritis chronic", "Chronic Pyelonephritis", "PYELONEPHRITIS CHRONIC", "PYELONEPHRITIS, CHRONIC", "pyelonephritis; chronic", "chronic; pyelonephritis", "pyelonephritis, chronic", "Chronic pyelonephritis NOS", "Pyelonephritis chronic NOS", "CPN - Chronic pyelonephritis", "Chronic pyelonephritis (disorder)", "chronic pyelonephritis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic pyelonephritis", "shortest_name_length": 22}
{"curie": "UMLS:C5237062", "names": ["Recurrent Endometrial Mucinous Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Endometrial Mucinous Adenocarcinoma", "shortest_name_length": 45}
{"curie": "MONDO:0004556", "names": ["carcinoma arising in nasal papillomatosis", "Carcinoma Arising in Nasal Papillomatosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma arising in nasal papillomatosis", "shortest_name_length": 41}
{"curie": "UMLS:C5190966", "names": ["HPV-Negative Squamous Cell Carcinoma", "Squamous cell carcinoma, HPV-negative", "Human papillomavirus negative squamous cell carcinoma", "Human Papillomavirus-Negative Squamous Cell Carcinoma", "Squamous cell carcinoma, HPV (human papillomavirus) negative", "Human papillomavirus negative squamous cell carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Human papillomavirus negative squamous cell carcinoma", "shortest_name_length": 36}
{"curie": "MONDO:0011552", "names": ["SCZD10", "SCHIZOPHRENIA 10", "schizophrenia 10", "Periodic catatonia", "catatonia, periodic", "CATATONIA, PERIODIC", "schizophrenic catatonia", "Catatonic Schizophrenia", "schizophrenia catatonic", "schizophrenic catalepsy", "catatonic schizophrenia", "Schizophrenic catatonia", "Schizophrenic catalepsy", "Catatonic schizophrenia", "schizophrenia; catatonic", "Schizophrenia, catatonic", "schizophrenic; catalepsy", "schizophrenia; catalepsy", "catatonic; schizophrenic", "Schizophrenia, Catatonic", "catalepsy; schizophrenic", "Catatonic Schizophrenias", "SCHIZOPHRENIA, CATATONIC", "Schizophrenias, Catatonic", "Catatonic schizophrenia, NOS", "Catatonic Type Schizophrenia", "Catatonic type schizophrenia", "catatonic schizophrenia type", "SCHIZOPHRENIA CATATONIC TYPE", "Schizophrenia, catatonic type", "Schizophrenic flexibilatis cerea", "DEMENTIA PRAECOX, CATATONIC TYPE", "Schizophrenic flexibilitas cerea", "flexibilitas cerea; schizophrenic", "schizophrenia; flexibilitas cerea", "Catatonic schizophrenia (disorder)", "catatonic; disorder, schizophrenic", "disorder; catatonic, schizophrenic", "[X]Schizophrenic flexibilatis cerea", "catatonic schizophrenia (diagnosis)", "SCHIZOPHRENIA SUSCEPTIBILITY LOCUS, CHROMOSOME 15q15-RELATED", "schizophrenia susceptibility locus, chromosome 15Q15-related"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schizophrenia 10", "shortest_name_length": 6}
{"curie": "MONDO:0007182", "names": ["MJD", "SCA3", "joseph disease", "Azorean Ataxia", "Joseph Disease", "Azorean disease", "disease josephs", "Machado disease", "Disease, Joseph", "Azorean Disease", "Disease, Azorean", "SPINOPONTINE ATROPHY", "Azorean disease, NOS", "Spinopontine atrophy", "Machado-Joseph Disease", "MACHADO-JOSEPH DISEASE", "disease joseph machado", "machado-joseph disease", "Joseph Azorean Disease", "Machado Joseph Disease", "disease machado joseph", "Machado Joseph disease", "machado joseph disease", "Machado-Joseph disease", "disease josephs machado", "Disease, Joseph Azorean", "disease machado josephs", "Disease, Machado-Joseph", "spinocerebellar ataxia 3", "Spinocerebellar Ataxia-3", "SPINOCEREBELLAR ATAXIA 3", "Spinocerebellar Ataxia 3", "Ataxia 3, Spinocerebellar", "spinocerebellar atrophy 3", "Spinocerebellar Ataxia 3s", "Portuguese-Azorean disease", "Azorean Neurologic Disease", "Azorean neurologic disease", "AZOREAN NEUROLOGIC DISEASE", "Azorean disease (disorder)", "Ataxia 3s, Spinocerebellar", "3s, Spinocerebellar Ataxia", "Spinocerebellar Atrophy III", "Neurologic Disease, Azorean", "Disease, Azorean Neurologic", "SPINOCEREBELLAR ATROPHY III", "Spinocerebellar Atrophy IIIs", "MJD - Machado-Joseph disease", "Atrophy III, Spinocerebellar", "III, Spinocerebellar Atrophy", "Spinocerebellar Ataxia Type 3", "Spinocerebellar ataxia type 3", "Atrophy IIIs, Spinocerebellar", "spinocerebellar ataxia type 3", "Type 3 Spinocerebellar Ataxia", "Machado Joseph Azorean Disease", "Spinocerebellar Atrophy Type 3", "Nervous System Azorean Disease", "Machado-Joseph Azorean Disease", "spinocerebellar atrophy type 3", "Nigrospinodentatal Degeneration", "Disease, Machado-Joseph Azorean", "NIGROSPINODENTATAL DEGENERATION", "Azorean Disease, Nervous System", "Azorean Disease (Machado-Joseph)", "Azorean Disease (Machado Joseph)", "Nigrospinodentatal Degenerations", "Degeneration, Nigrospinodentatal", "Degenerations, Nigrospinodentatal", "Disease, Azorean (Machado-Joseph)", "Azorean disease of the nervous system", "autosomal dominant striatonigral degeneration", "Autosomal Dominant Striatonigral Degeneration", "Striatonigral Degeneration, Autosomal Dominant", "Nigro-spino-dentatal degeneration with nuclear ophthalmoplegia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Machado-Joseph disease", "shortest_name_length": 3}
{"curie": "MONDO:0023040", "names": ["ectodermal dysplasia Bartalos type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ectodermal dysplasia Bartalos type", "shortest_name_length": 34}
{"curie": "MONDO:0011000", "names": ["GC-E", "GUCY2E", "GUCY2EP", "guanylate cyclase 2E", "GUANYLATE CYCLASE 2E", "GUCY2D, MOUSE, HOMOLOG OF", "guanylate cyclase type 2E", "Gucy2D, mouse, homolog of", "GUANYLATE CYCLASE 2E, PSEUDOGENE", "guanylate cyclase 2E, pseudogene", "GUANYLYL CYCLASE, MEMBRANE, TYPE E", "guanylyl cyclase, Membrane, type E"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "guanylate cyclase 2E", "shortest_name_length": 4}
{"curie": "UMLS:C2347917", "names": ["Recurrent Spinal Cord Tumor", "Recurrent Spinal Cord Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Spinal Cord Neoplasm", "shortest_name_length": 27}
{"curie": "MONDO:0010556", "names": ["CPXD", "Calcinosis universalis", "calcinosis universalis", "calcinosis cutis universalis", "Calcinosis universalis (disorder)", "X-linked chondrodysplasia punctata", "chondrodysplasia punctata, X-linked", "X-linked chondrodysplasia punctata 1", "chondrodystrophia calcificans congenita", "calcinosis cutis universalis (diagnosis)", "X-linked dominant chondrodysplasia punctata", "chondrodysplasia punctata, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "X-linked chondrodysplasia punctata", "shortest_name_length": 4}
{"curie": "UMLS:C3272435", "names": ["Ampullary High Grade Intraepithelial Neoplasia", "Ampullary Noninvasive Pancreatobiliary Papillary Neoplasm with High Grade Dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ampullary Noninvasive Pancreatobiliary Papillary Neoplasm with High Grade Dysplasia", "shortest_name_length": 46}
{"curie": "MONDO:0016149", "names": ["qualitative or quantitative defects of merosin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of merosin", "shortest_name_length": 46}
{"curie": "MONDO:0004197", "names": ["male urethra cancer", "male urethral cancer", "cancer of male urethra", "malignant male urethra neoplasm", "Male Urethral Malignant Neoplasm", "Male urethral malignant neoplasm", "malignant neoplasm of male urethra"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "male urethral cancer", "shortest_name_length": 19}
{"curie": "MONDO:0006717", "names": ["DF", "histiocytoma", "histiocytomas", "Dermatofibroma", "dermatofibroma", "DERMATOFIBROMA", "dermatofibromas", "Dermatofibromas", "Sclerosing angioma", "sclerosing angioma", "Sclerosing Angioma", "Dermatofibroma NOS", "Pleomorphic fibroma", "pleomorphic fibroma", "Pleomorphic Fibroma", "Dermatofibroma, NOS", "Sclerosing Angiomas", "Angioma, Sclerosing", "Angiomas, Sclerosing", "Sclerosing Hemangioma", "[M]Dermatofibroma NOS", "sclerosing hemangioma", "Cutaneous Histiocytoma", "Sclerosing Hemangiomas", "Hemangioma, Sclerosing", "Fibrohistiocytic tumor", "Cutaneous histiocytoma", "cutaneous histiocytoma", "fibrohistiocytic tumor", "Fibrohistiocytic tumour", "Cutaneous Histiocytomas", "Hemangiomas, Sclerosing", "Histiocytoma, Cutaneous", "fibrous xanthoma of skin", "Fibrous xanthoma of skin", "Histiocytomas, Cutaneous", "fibrohistiocytic neoplasm", "Dermatofibroma (disorder)", "Skin Fibrous Histiocytoma", "Dermatofibroma lenticulare", "Sclerosing angioma of skin", "sclerosing angioma of skin", "fibrous histiocytoma of skin", "Fibrous histiocytoma of skin", "Fibrous Histiocytoma of Skin", "Subepidermal nodular fibrosis", "Skin Fibrohistiocytic Neoplasm", "Fibrohistiocytic tumor of skin", "Cutaneous Fibrous Histiocytoma", "Pleomorphic fibroma (disorder)", "cutaneous fibrous histiocytoma", "skin neoplasm fibrohistiocytic", "Fibrohistiocytic tumour of skin", "Benign Skin Fibrous Histiocytoma", "Fibrous Histiocytoma of the Skin", "fibrous histiocytoma of the skin", "benign skin fibrous histiocytoma", "dermatofibroma, no ICD-O subtype", "Cutaneous Fibrohistiocytic Neoplasm", "Benign Fibrous Histiocytoma of Skin", "Benign fibrous histiocytoma of skin", "benign fibrous histiocytoma of skin", "fibrohistiocytic neoplasm (diagnosis)", "benign cutaneous fibrous histiocytoma", "Benign Fibrous Cutaneous Histiocytoma", "benign fibrous cutaneous histiocytoma", "benign Cutaneous fibrous Histiocytoma", "Benign Cutaneous Fibrous Histiocytoma", "Sclerosing angioma of skin (disorder)", "Fibrous histiocytoma of skin (disorder)", "Benign Fibrous Histiocytoma of the Skin", "benign fibrous histiocytoma of the skin", "Dermatofibroma (morphologic abnormality)", "Fibrohistiocytic tumor of skin (disorder)", "Sclerosing angioma (morphologic abnormality)", "sclerosing angioma (morphologic abnormality)", "Pleomorphic fibroma (morphologic abnormality)", "dermatofibroma, no ICD-O subtype (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cutaneous fibrous histiocytoma", "shortest_name_length": 2}
{"curie": "MONDO:0004838", "names": ["postural proteinuria", "Albuminuria;postural", "Postural albuminuria", "postural albuminuria", "Postural proteinuria", "Proteinuria;postural", "postural; albuminuria", "postural; proteinuria", "Proteinuria, postural", "albuminuria; postural", "proteinuria; postural", "Albuminuria, postural", "Proteinuria;orthostatic", "orthostatic albuminuria", "Albuminuria;orthostatic", "Orthostatic albuminuria", "orthostatic proteinuria", "Orthostatic proteinuria", "proteinuria; orthostatic", "orthostatic; albuminuria", "orthostatic; proteinuria", "Albuminuria, orthostatic", "Proteinuria, orthostatic", "albuminuria; orthostatic", "Benign postural proteinuria", "benign postural proteinuria", "Orthostatic proteinuria (finding)", "orthostatic proteinuria (diagnosis)", "Orthostatic albuminuria/proteinuria", "Orthostatic proteinuria, unspecified", "benign postural proteinuria (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orthostatic proteinuria", "shortest_name_length": 20}
{"curie": "UMLS:C1336274", "names": ["Stage III Thyroid Medullary Carcinoma", "Stage III Thyroid Gland Medullary Cancer", "Stage III Medullary Carcinoma of Thyroid", "Stage III Thyroid Gland Medullary Carcinoma", "Stage III Medullary Thyroid Gland Carcinoma", "Stage III Medullary Carcinoma of the Thyroid", "Stage III Medullary Carcinoma of Thyroid Gland", "Stage III Medullary Carcinoma of the Thyroid Gland", "Stage III Thyroid Gland Medullary Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Thyroid Gland Medullary Carcinoma AJCC v7", "shortest_name_length": 37}
{"curie": "UMLS:C1336440", "names": ["Stage IV Small Cell Lung Cancer", "Stage IV Small Cell Lung Carcinoma", "Stage IV Small Cell Carcinoma of Lung", "Stage IV Small Cell Carcinoma of the Lung", "Stage IV Lung Small Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Lung Small Cell Carcinoma AJCC v7", "shortest_name_length": 31}
{"curie": "UMLS:C1335968", "names": ["dVIN", "d-VIN", "SxVIN", "Vulvar intraepithelial neoplasia NOS", "Vulvar Carcinoma In Situ of Simplex Type", "Vulvar Intraepithelial Neoplasia, Simplex", "Differentiated Vulvar Intraepithelial Neoplasia", "Differentiated vulvar intraepithelial neoplasia", "Vulvar Intraepithelial Neoplasia, Differentiated", "Vulvar Intraepithelial Neoplasia, HPV-Independent", "Differentiated-type vulvar intraepithelial neoplasia", "Differentiated VIN (vulvar intraepithelial neoplasia)", "Vulvar Intraepithelial Neoplasia, Differentiated Type", "Vulvar intraepithelial neoplasia Not Otherwise Specified", "Simplex (Differentiated) Vulvar Intraepithelial Neoplasia", "Vulvar Intraepithelial Neoplasia, Differentiated (Simplex)", "Differentiated vulvar intraepithelial neoplasia (disorder)", "Vulvar Intraepithelial Neoplasia, Differentiated (Simplex) Type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Differentiated vulvar intraepithelial neoplasia", "shortest_name_length": 4}
{"curie": "MONDO:0016185", "names": ["qualitative or quantitative defects of protein O-mannosyltransferase 2", "qualitative or quantitative defects of protein O-mannosyltransferase type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of protein O-mannosyltransferase 2", "shortest_name_length": 70}
{"curie": "UMLS:C5557383", "names": ["Vulvar Rhabdomyoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vulvar Rhabdomyoma", "shortest_name_length": 18}
{"curie": "MONDO:0000685", "names": ["Visual Agnosia", "VISUAL AGNOSIA", "Agnosia Visual", "Visual agnosia", "visual agnosia", "agnosia visual", "Visual amnesia", "Visual Agnosias", "Agnosia, Visual", "visual agnosias", "Agnosia, visual", "Agnosias, Visual", "Primary visual agnosia", "visuoperceptual agnosia", "Visuoperceptual agnosia", "Monomodal visual amnesia", "visual agnosia was noted", "visual agnosia (disease)", "Visual agnosia (disorder)", "visual agnosia (diagnosis)", "visual agnosia (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "visual agnosia", "shortest_name_length": 14}
{"curie": "MONDO:0009525", "names": ["Shsf3", "SHFM3", "SHSF3", "Buttiens-Fryns syndrome", "Buttiens Fryns syndrome", "split hand-foot malformation 3", "split-hand/foot malformation 3", "Split-Hand Foot Malformation 3", "Split-Hand/Foot Malformation 3", "SPLIT-HAND/FOOT MALFORMATION 3", "10q24 microduplication syndrome", "split hand-foot malformation type 3", "Split-Hand/Foot Malformation Type 3", "split-hand/foot malformation type 3", "chromosome 10q24 duplication syndrome", "CHROMOSOME 10q24 DUPLICATION SYNDROME", "chromosome 10Q24 Duplication syndrome", "distal limb deficiencies with micrognathia", "limb deficiencies distal with micrognathia", "limb deficiencies, distal, with micrognathia", "LIMB DEFICIENCIES, DISTAL, WITH MICROGNATHIA", "Limb Deficiencies, Distal, with Micrognathia", "distal limb deficiencies-micrognathia syndrome", "Distal limb deficiencies-micrognathia syndrome", "Distal limb deficiency with micrognathia syndrome", "split-hand/foot malformation 3, gene duplication syndrome", "Distal limb deficiency with micrognathia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "split hand-foot malformation 3", "shortest_name_length": 5}
{"curie": "MONDO:0002009", "names": ["MDD", "major depression", "MAJOR DEPRESSION", "Major depression", "Major Depression", "depression unipolar", "UNIPOLAR DEPRESSION", "Unipolar depression", "clinical depression", "Unipolar Depression", "unipolar depression", "Depression, Unipolar", "Major depression NOS", "Unipolar Depressions", "Major depression, NOS", "Depressions, Unipolar", "major depressive episode", "Major depressive illness", "major depressive illness", "Major depressive disorder", "MAJOR DEPRESSIVE DISORDER", "Major Depressive Disorder", "DEPRESSIVE DISORDER MAJOR", "major depressive disorder", "depressive; episode, major", "Depressive Disorder, Major", "Recurrent major depression", "recurrent major depression", "Major Depressive Disorders", "Unipolar depressive illness", "Depressive Disorders, Major", "major depressive disorder 1", "major depressive disorder 2", "Major depressive disorder NOS", "Major depressive disorder, NOS", "single major depressive episode", "Recurrent major depression, NOS", "major depression, single episode", "Major depression, single episode", "single episode of major depression", "Recurrent major depressive disorder", "Recurrent major depressive episodes", "major depression recurrent episodes", "DEPRESSIVE DISORDER MAJOR RECURRENT", "Major depressive disorder, recurrent", "Major depressive disorder (disorder)", "Recurrent major depression (disorder)", "Major depressive disorder (diagnosis)", "Major depression, single episode, NOS", "recurrent major depression (diagnosis)", "unipolar depression, susceptibility to", "recurrent episodes of major depression", "Recurrent major depressive disorder, NOS", "DEPRESSIVE DISORDER MAJOR SINGLE EPISODE", "Major depressive disorder; single episode", "Major depressive disorder, single episode", "Single Episode of Major Depressive Disorder", "Major depression, single episode (disorder)", "Major depressive disorder, recurrent episode", "major depression, single episode (diagnosis)", "Major depressive disorder; recurrent episode", "major depressive disorder, recurrent episode", "Recurrent major depressive episodes (disorder)", "Recurrent major depressive episodes (diagnosis)", "Major depressive disorder, recurrent, unspecified", "Major depressive disorder, single episode, unspecified", "Major depressive disorder, Recurrent episode, Unspecified", "major depressive disorder, response to citalopram therapy in", "Major depressive disorder, single episode, unspecified degree", "Major depressive affective disorder, single episode, unspecified", "Major depressive disorder, recurrent episode, unspecified degree", "Major depressive affective disorder, recurrent episode, unspecified", "major depressive disorder and accelerated response to antidepressant drug treatment"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "major depressive disorder", "shortest_name_length": 3}
{"curie": "MONDO:0011819", "names": ["SCA22", "SCA19", "SCA19/22", "SCA 19/22", "Spinocerebellar ataxia 19", "SPINOCEREBELLAR ATAXIA 19", "Spinocerebellar ataxia 22", "spinocerebellar ataxia 22", "SPINOCEREBELLAR ATAXIA 22", "spinocerebellar ataxia 19", "spinocerebellar ataxia type 19", "Spinocerebellar ataxia type 19", "SCA19 Spinocerebellar ataxia 19", "spinocerebellar ataxia 19 and 22", "Spinocerebellar ataxia type 19/22", "Spinocerebellar Ataxia Type 19/22", "spinocerebellar ataxia type 19/22", "Spinocerebellar ataxia type 19 (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spinocerebellar ataxia type 19/22", "shortest_name_length": 5}
{"curie": "MONDO:0015335", "names": ["orofacial clefting syndrome", "Mendelian syndromes with cleft lip/palate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mendelian syndromes with cleft lip/palate", "shortest_name_length": 27}
{"curie": "MONDO:0014395", "names": ["FTDALS2", "frontotemporal dementia and/or amyotrophic lateral sclerosis-2", "frontotemporal dementia and/or amyotrophic lateral sclerosis 2", "FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 2", "frontotemporal dementia and/or amyotrophic lateral sclerosis type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontotemporal dementia and/or amyotrophic lateral sclerosis 2", "shortest_name_length": 7}
{"curie": "UMLS:C1301034", "names": ["PanIN", "Pancreatic Dysplasia", "Pancreatic Intraepithelial Neoplasia", "Pancreatic intraepithelial neoplasia", "Pancreatic intraepithelial neoplasia (PanIN)", "Pancreatic intraepithelial neoplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic intraepithelial neoplasia", "shortest_name_length": 5}
{"curie": "UMLS:C4086782", "names": ["Recurrent HRMDS", "Relapsed or Refractory HRMDS", "Recurrent Myelodysplastic Syndrome", "Relapsed or Refractory High-Risk Myelodysplastic Syndrome", "Recurrent Acute Myeloid Leukemia with Myelodysplasia-Related Changes", "Recurrent Acute Myeloid Leukemia (AML) with Myelodysplasia-Related Changes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Acute Myeloid Leukemia with Myelodysplasia-Related Changes", "shortest_name_length": 15}
{"curie": "MONDO:0006525", "names": ["Contact allergy", "Allergic contact dermatitis", "dermatitis contact allergic", "Dermatitis contact/allergic", "allergic contact dermatitis", "contact allergic dermatitis", "Allergic Contact Dermatitis", "contact dermatitis allergic", "Contact Dermatitis, Allergic", "Dermatitis, Allergic Contact", "dermatitis; contact, allergic", "Allergic Contact Dermatitides", "contact; dermatitis, allergic", "Dermatitis, Contact, Allergic", "Allergic Eczematous Dermatitis", "Dermatitides, Allergic Contact", "Contact Dermatitides, Allergic", "Dermatitis, Allergic Eczematous", "Eczematous Dermatitis, Allergic", "Allergic Eczematous Dermatitides", "Dermatitides, Allergic Eczematous", "ACD - Allergic contact dermatitis", "Eczematous Dermatitides, Allergic", "allergic form of contact dermatitis", "Allergic contact dermatitis (disorder)", "allergic contact dermatitis (diagnosis)", "Allergic contact dermatitis, unspecified cause"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "allergic contact dermatitis", "shortest_name_length": 15}
{"curie": "MONDO:0001952", "names": ["parietal lobe cancer", "tumor of Parietal Lobe", "parietal lobe neoplasm", "cancer of parietal lobe", "malignant parietal lobe neoplasm", "Malignant neoplasm of parietal lobe", "malignant neoplasm of parietal lobe", "Malignant neoplasm of parietal lobe (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "parietal lobe cancer", "shortest_name_length": 20}
{"curie": "MONDO:0003568", "names": ["Chiasma syndrome", "chiasma syndrome", "chiasmal syndrome", "Chiasmal syndrome", "optic chiasm disorder", "optic chiasma disease", "Optic chiasm disorder", "disease of optic chiasma", "disorder of optic chiasm", "chiasmal optic; disorder", "Disorders of optic chiasm", "disorder of optic chiasma", "Optic chiasm disorder (disorder)", "optic chiasma disease or disorder", "disorder of optic chiasm (diagnosis)", "disease or disorder of optic chiasma", "disease (or disorder); chiasmal optic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of optic chiasm", "shortest_name_length": 16}
{"curie": "UMLS:C0473221", "names": ["Cryoglobulinemic glomerulonephritis", "Cryoglobulinemic Glomerulonephritis", "Cryoglobulinaemic glomerulonephritis", "Cryoglobulinemic glomerulonephritis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cryoglobulinemic glomerulonephritis", "shortest_name_length": 35}
{"curie": "UMLS:C2674636", "names": ["Familial GIST", "Familial GIST Syndrome", "Familial Gastrointestinal Stromal Tumor", "GASTROINTESTINAL STROMAL TUMOR, FAMILIAL"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "GASTROINTESTINAL STROMAL TUMOR, FAMILIAL", "shortest_name_length": 13}
{"curie": "UMLS:C1706732", "names": ["Advanced Adult Hepatoma", "Advanced Hepatocellular Cancer", "Advanced Adult Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Adult Hepatocellular Carcinoma", "shortest_name_length": 23}
{"curie": "MONDO:0016392", "names": ["cerebellar hypoplasia tapetoretinal degeneration", "cerebellar hypoplasia-tapetoretinal degeneration syndrome", "cerebellar hyplasia/atrophy, epilepsy, and global developmental delay"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellar hypoplasia-tapetoretinal degeneration syndrome", "shortest_name_length": 48}
{"curie": "MONDO:0008581", "names": ["ECTOPIC ERUPTION OF TEETH", "ectopic eruption of teeth", "malposition of teeth with or without hypodontia/oligodontia", "MALPOSITION OF TEETH WITH OR WITHOUT HYPODONTIA/OLIGODONTIA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malposition of teeth with or without hypodontia/oligodontia", "shortest_name_length": 25}
{"curie": "UMLS:C0003875", "names": ["Arthritis viral", "Viral Arthritis", "Viral arthritis", "viral arthritis", "Arthritis;viral", "ARTHRITIS, VIRAL", "Arthritis, Viral", "Arthritis viral NOS", "viral arthritis (diagnosis)", "Arthritis due to viral infection", "Arthritis caused by viral infection", "Arthritis caused by viral infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Arthritis, Viral", "shortest_name_length": 15}
{"curie": "UMLS:C1332516", "names": ["Benign Soft Tissue Mediastinal Tumor", "Benign Mediastinal Soft Tissue Neoplasm", "Benign Soft Tissue Tumor of Mediastinum", "Benign Soft Tissue Neoplasm of Mediastinum", "Benign Soft Tissue Tumor of the Mediastinum", "Benign Soft Tissue Neoplasm of the Mediastinum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Mediastinal Soft Tissue Neoplasm", "shortest_name_length": 36}
{"curie": "EFO:0005938", "names": ["congenital left-sided heart lesions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital left-sided heart lesions", "shortest_name_length": 35}
{"curie": "MONDO:0002197", "names": ["minor vestibular gland adenoma", "minor vestibular glands adenoma", "adenoma of minor vestibular glands", "Adenoma of Minor Vestibular Glands"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "minor vestibular glands adenoma", "shortest_name_length": 30}
{"curie": "MONDO:0000734", "names": ["Ohdo syndrome", "Ohdo syndrome and variants", "Ohdo blepharophimosis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ohdo syndrome and variants", "shortest_name_length": 13}
{"curie": "MONDO:0025412", "names": ["Cat plague", "Cat Plague", "Show Fever", "show fever", "Cat Plagues", "Plague, Cat", "show fevers", "plague, Cat", "Fever, Show", "fever, show", "Show Fevers", "Fevers, Show", "fevers, show", "plagues, Cat", "Plagues, Cat", "Feline ataxia", "Feline Ataxia", "ataxia, Feline", "Feline Ataxias", "Ataxia, Feline", "ataxias, Feline", "Ataxias, Feline", "Feline distemper", "Feline Distemper", "Feline Distempers", "Distemper, Feline", "distemper, Feline", "Distempers, Feline", "distempers, Feline", "feline panleukopenia", "Feline Panleukopenia", "Feline panleukopenia", "Feline panleucopenia", "Feline Panleukopenias", "Panleukopenia, Feline", "Feline Agranulocytoses", "Feline agranulocytosis", "Panleukopenias, Feline", "Feline Agranulocytosis", "agranulocytoses, Feline", "Agranulocytosis, Feline", "Agranulocytoses, Feline", "agranulocytosis, Feline", "Feline infectious enteritis", "Feline Infectious Enteritis", "Feline parvovirus infection", "enteritis, Feline infectious", "Infectious Enteritis, Feline", "Enteritis, Feline Infectious", "infectious enteritis, Feline", "Feline Infectious Enteritides", "Feline infectious Enteritides", "enteritides, Feline infectious", "Infectious Enteritides, Feline", "infectious Enteritides, Feline", "Enteritides, Feline Infectious", "Infectious feline panleucopenia", "Feline panleukopenia (disorder)", "Infectious feline panleukopenia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "feline panleukopenia", "shortest_name_length": 10}
{"curie": "MONDO:0005181", "names": ["cpeo", "CPEO", "Graefe Disease", "Disease, Graefe", "Graefe's Disease", "Graefe's disease", "EXTRAOCULAR PALSY", "Extraocular palsy", "Palsy extraocular", "PALSY EXTRAOCULAR", "OPHTHALMOPLEGIA EXTERNA", "Ophthalmoplegia externa", "External Ophthalmoplegia", "External ophthalmoplegia", "external ophthalmoplegia", "external; ophthalmoplegia", "Maternally-inherited CPEO", "ophthalmoplegia; external", "External Ophthalmoplegias", "Ophthalmoplegia, external", "Ocular Muscular Dystrophy", "Ophthalmoplegia, External", "Ophthalmoplegias, External", "Muscular Dystrophy, Ocular", "Dystrophy, Ocular Muscular", "Ocular Muscular Dystrophies", "Muscular Dystrophies, Ocular", "External ophthalmoplegia NOS", "Mitochondrial Ocular Myopathy", "Myopathy, Mitochondrial Ocular", "Ocular Myopathy, Mitochondrial", "Ocular myopathy, von Graefe-Fuchs", "Ophthalmoplegia syndrome, external", "Chronic progressive ophthalmoplegia", "External ophthalmoplegia (disorder)", "Ocular Myopathy of Von Graefe Fuchs", "Ocular Myopathy of Von Graefe-Fuchs", "progressive external ophthalmoplegia", "Progressive External Ophthalmoplegia", "Progressive external ophthalmoplegia", "Paralysis of the extraocular muscles", "external ophthalmoplegia (diagnosis)", "Ophthalmoplegia, progressive external", "Ophthalmoplegia, Progressive External", "External ophthalmoplegia, progressive", "ophthalmoplegia; progressive external", "External Ophthalmoplegia, Progressive", "progressive; ophthalmoplegia, external", "PEO - Progressive external ophthalmoplegia", "External ophthalmoplegia, progressive (PEO)", "Chronic progressive external ophthalmoplegia", "chronic external progressive ophthalmoplegia", "Chronic Progressive External Ophthalmoplegia", "chronic progressive external ophthalmoplegia", "Ophthalmoplegia, Chronic Progressive External", "Progressive external ophthalmoplegia (disorder)", "mtDNA-related progressive external ophthalmoplegia", "CPEO - chronic progressive external ophthalmoplegia", "chronic progressive external ophthalmoplegia (CPEO)", "Progressive muscular dystrophy, ophthalmoplegic type", "chronic progressive external ophthalmoplegia (diagnosis)", "chronic progressive paralysis of the external eye muscle", "chronic progressive external ophthalmoplegia [ambiguous]", "Progressive paralysis or weakness of muscles of eye movement", "Progressive paralysis or weakness of muscles of eye motility", "Mitochondrial DNA-related progressive external ophthalmoplegia", "Maternally-inherited chronic progressive external ophthalmoplegia", "Paralysis or weakness of muscles within or surrounding outer part of eye"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive external ophthalmoplegia", "shortest_name_length": 4}
{"curie": "MONDO:0005244", "names": ["Neuropathy", "neuropathy", "NEUROPATHY", "neuropathies", "Neuropathy NOS", "nerve disorders", "nerve; disorder", "Neuropathy, NOS", "NEUROPATHY - (NOS)", "Peripheral neuritis", "disorders neuropathy", "Peripheral Neuropathy", "Neuropathy (disorder)", "Peripheral neuropathy", "peripheral neuropathy", "PERIPHERAL NEUROPATHY", "Neuropathy;peripheral", "neuropathy (diagnosis)", "Peripheral nerve damage", "Neuropathy (nerve damage)", "peripheral nerve disorder", "Peripheral Nerve Disorder", "PN - Peripheral neuropathy", "nerve disorders (diagnosis)", "peripheral neuropathy (diagnosis)", "peripheral neuropathy (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peripheral neuropathy", "shortest_name_length": 10}
{"curie": "MONDO:0013299", "names": ["chromosome 6Q13-q14 deletion syndrome", "CHROMOSOME 6q11-q14 DELETION SYNDROME", "chromosome 6q11-q14 deletion syndrome", "CHROMOSOME 6q13-q14 DELETION SYNDROME", "chromosome 6q11-q14 deletion syndrome, isolated cases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 6q11-q14 deletion syndrome", "shortest_name_length": 37}
{"curie": "UMLS:C1321581", "names": ["Bezoar", "bezoar", "BEZOAR", "bezoars", "Bezoar disorder", "Bezoar (disorder)", "bezoars (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bezoar disorder", "shortest_name_length": 6}
{"curie": "UMLS:C0235919", "names": ["Nerve root lesion", "nerve root lesion", "NERVE ROOT LESION", "NERVE ROOT LIAISON", "lesions nerve root", "Nerve root lesion NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nerve root lesion", "shortest_name_length": 17}
{"curie": "MONDO:0022025", "names": ["Boylan Dew Greco syndrome", "boylan dew greco syndrome", "Congenital hypomyelination neuropathy with arthrogryposis multiplex congenita", "congenital hypomyelination neuropathy with arthrogryposis multiplex congenita"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "boylan dew greco syndrome", "shortest_name_length": 25}
{"curie": "MONDO:0000212", "names": ["Infantile hypercalcemia", "infantile hypercalcemia", "Infantile hypercalcaemia", "hypercalcemia, infantile", "Hypercalcemia, Infantile", "infantile hypercalcemia disease", "obsolete Infantile hypercalcemia", "hypercalcemia disease of infancy", "Infantile hypercalcemia (disorder)", "idiopathic infantile hypercalcemia", "Idiopathic Infantile Hypercalcemia", "infantile onset hypercalcemia disease", "hypercalcemia, idiopathic, of infancy", "autosomal recessive infantile hypercalcemia", "Autosomal Recessive Infantile Hypercalcemia", "Autosomal recessive infantile hypercalcemia", "autosomal recessive hypercalcemia, infantile", "Autosomal recessive infantile hypercalcaemia", "hypercalcemia, infantile, autosomal recessive", "Autosomal recessive infantile hypercalcemia (disorder)", "Familial infantile hypercalcemia with suppressed intact parathyroid hormone", "familial infantile hypercalcemia with suppressed intact parathyroid hormone", "Familial infantile hypercalcaemia with suppressed intact parathyroid hormone"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypercalcemia, infantile", "shortest_name_length": 23}
{"curie": "MONDO:0030490", "names": ["OOMD11", "oocyte maturation defect 11", "OOCYTE MATURATION DEFECT 11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oocyte maturation defect 11", "shortest_name_length": 6}
{"curie": "UMLS:C4726592", "names": ["Recurrent Burkitt Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Burkitt Leukemia", "shortest_name_length": 26}
{"curie": "MONDO:0018261", "names": ["Nevada syndrome", "Nevus epidermicus verrucosus with angiodysplasia and aneurysms"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nevada syndrome", "shortest_name_length": 15}
{"curie": "UMLS:C0015207", "names": ["Eventrated", "eventration", "Eventration", "EVENTRATION", "eventrations", "Eventration, NOS", "Eventration (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eventration", "shortest_name_length": 10}
{"curie": "MONDO:0004609", "names": ["HSV", "Herpes", "HSV infection", "HSV Infection", "herpes simplex", "Herpes Simplex", "Herpes simplex", "HERPES SIMPLEX", "simplex herpes", "herpes; simplex", "simplex; herpes", "Herpes simplex NOS", "Herpes simplex, NOS", "Herpes Simplex Virus", "Herpes simplex complex", "Herpes simplex disease", "herpes simplex complex", "diseases herpes simplex", "infection herpes simplex", "HERPES SIMPLEX INFECTION", "herpes simplex infection", "Herpes simplex infection", "herpes infections simplex", "Herpes simplex (disorder)", "Herpesvirus hominis disease", "Herpes simplex infection NOS", "Herpes Simplex Virus Infection", "Herpes simplex virus infection", "Herpes simplex viral infection", "herpes simplex viral infection", "herpes simplex virus infection", "Simplexvirus infectious disease", "Simplexvirus disease or disorder", "herpes simplex infectious disease", "infection due to Herpes simplex virus", "Herpes simplex (excluding F85 X90 Y72)", "Herpesviral [herpes simplex] infections", "Simplexvirus caused disease or disorder", "infection due to Herpes simplex virus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "herpes simplex infectious disease", "shortest_name_length": 3}
{"curie": "UMLS:C5239114", "names": ["Refractory Follicular T-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Follicular T-Cell Lymphoma", "shortest_name_length": 37}
{"curie": "MONDO:0019413", "names": ["Ischiospinal dysostosis", "Ischiovertebral syndrome", "ischio-spinal dysostosis", "Ischio-spinal dysostosis", "Ischio-vertebral syndrome", "Ischiovertebral dysplasia", "ischio-vertebral syndrome", "Ischio-vertebral dysplasia", "ischio-vertebral dysplasia", "Ischio-vertebral syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ischio-vertebral syndrome", "shortest_name_length": 23}
{"curie": "UMLS:C4688334", "names": ["Childhood Refractory Malignant Solid Tumor", "Childhood Refractory Malignant Solid Neoplasm", "Refractory Childhood Malignant Solid Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Childhood Refractory Malignant Solid Neoplasm", "shortest_name_length": 42}
{"curie": "UMLS:C1708194", "names": ["Gastric Granular Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gastric Granular Cell Tumor", "shortest_name_length": 27}
{"curie": "UMLS:C0160705", "names": ["IVC injury", "Inferior vena cava injury", "injury; inferior vena cava", "Injury of inferior vena cava", "Injury to Inferior Vena Cava", "Injury to inferior vena cava", "injury of inferior vena cava", "Injury of inferior vena cava, NOS", "v.cava; injury, inferior vena cava", "Injury of inferior vena cava (disorder)", "injury of inferior vena cava (diagnosis)", "Unspecified injury of inferior vena cava", "Injury to inferior vena cava, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Injury to Inferior Vena Cava", "shortest_name_length": 10}
{"curie": "MONDO:0010700", "names": ["Optic Atrophy Spastic Paraplegia Syndrome", "OPTIC ATROPHY--SPASTIC PARAPLEGIA SYNDROME", "optic atrophy--spastic paraplegia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "optic atrophy--spastic paraplegia syndrome", "shortest_name_length": 41}
{"curie": "MONDO:0009635", "names": ["MVD", "IDI", "MVID", "MVID1", "DIAR2", "Davidson disease", "DAVIDSON DISEASE", "Davidson's disease", "Microvillous atrophy", "MYO5B secretory diarrhea", "microvillus inclusion disease", "Microvillus inclusion disease", "Microvillous inclusion disease", "congenital microvillus atrophy", "microvillous inclusion disease", "Congenital microvillus atrophy", "microvillus atrophy, congenital", "congenital microvillous atrophy", "intractable diarrhea of infancy", "MICROVILLUS INCLUSION DISEASE 1", "Microvillus atrophy, congenital", "Congenital microvillous atrophy", "Intractable diarrhea of infancy", "MICROVILLUS ATROPHY, CONGENITAL", "familial enteropathy, microvillus", "diarrhea 2 with microvillus atrophy", "Diarrhea 2, With Microvillus Atrophy", "DIARRHEA 2, WITH MICROVILLUS ATROPHY", "diarrhea 2, with microvillus atrophy", "congenital familial protracted diarrhea", "Congenital microvillous atrophy (disorder)", "secretory diarrhea caused by mutation in MYO5B", "anomalies of intestine microvillus inclusion disease", "anomalies of intestine microvillus inclusion disease (diagnosis)", "DIARRHEA 2, WITH MICROVILLUS ATROPHY, WITH OR WITHOUT CHOLESTASIS", "congenital familial protracted diarrhea with enterocyte brush-border abnormalities", "congenital familial protracted diarrhea with enterocyte Brush-border abnormalities", "Congenital Familial Protracted Diarrhea With Enterocyte Brush-Border Abnormalities", "CONGENITAL FAMILIAL PROTRACTED DIARRHEA WITH ENTEROCYTE BRUSH-BORDER ABNORMALITIES"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microvillus inclusion disease", "shortest_name_length": 3}
{"curie": "UMLS:C4684834", "names": ["Refractory B Acute Lymphoblastic Leukemia", "Refractory B-Cell Acute Lymphoblastic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory B Acute Lymphoblastic Leukemia", "shortest_name_length": 41}
{"curie": "UMLS:C4527333", "names": ["Refractory Breast Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Breast Lymphoma", "shortest_name_length": 26}
{"curie": "MONDO:0016072", "names": ["genetic anomaly of puberty or/and menstrual cycle", "anomaly of puberty or/and menstrual cycle of genetic origin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anomaly of puberty or/and menstrual cycle of genetic origin", "shortest_name_length": 49}
{"curie": "UMLS:C0006107", "names": ["commotio", "CONCUSSION", "concussion", "Concussion", "concussions", "brain; blast", "Concussion NOS", "brain; commotio", "commotio; brain", "commotio cerebri", "Brain concussion", "Commotio Cerebri", "brain concussion", "Commotio cerebri", "Brain Concussion", "Concussion, Brain", "concussion; brain", "brain; concussion", "BRAIN, CONCUSSION", "brain concussions", "Brain Concussions", "Brain--Concussion", "cerebri; commotio", "Concussive injury", "Concussion (Brain)", "concussion disorder", "Cerebral Concussion", "cerebral concussion", "Cerebral concussion", "Cerebral Concussions", "cerebral; concussion", "concussion; cerebral", "Concussion, Cerebral", "concussion (diagnosis)", "Concussion, unspecified", "concussion injury of brain", "Concussion injury of brain", "Mild traumatic brain injury", "MTBI - Mild traumatic brain injury", "Concussion injury of brain (disorder)", "concussion injury of brain (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brain Concussion", "shortest_name_length": 8}
{"curie": "MONDO:0009315", "names": ["Hageman Trait", "F12 deficiency", "F12 DEFICIENCY", "HAF DEFICIENCY", "Haf deficiency", "defect; Hageman", "Hageman; defect", "Deficiency, Hageman", "deficiency, Hageman", "factor 12 deficiency", "Factor 12 Deficiency", "Deficiency, Factor 12", "factor XII deficiency", "Factor XII deficiency", "FACTOR XII DEFICIENCY", "factor xii deficiency", "Factor XII Deficiency", "Deficiency, Factor XII", "Factor 12 Deficiencies", "Deficiency, factor XII", "Factor XII Deficiencies", "Deficiencies, Factor 12", "Factor Twelve Deficiency", "Deficiencies, Factor XII", "Hageman factor deficiency", "Hageman Factor deficiency", "HAGEMAN FACTOR DEFICIENCY", "hageman factor deficiency", "Deficiency, Factor Twelve", "Hageman Factor Deficiency", "Deficiency, Hageman Factor", "Hageman factor; deficiency", "deficiency; Hageman factor", "Factor Deficiency, Hageman", "Factor Twelve Deficiencies", "Reduced factor XII activity", "Deficiencies, Factor Twelve", "factor XII deficiency disease", "Factor XII deficiency disease", "coagulation factor 12 deficiency", "congenital factor XII deficiency", "Congenital factor XII deficiency", "Coagulation Factor 12 Deficiency", "Factor XII deficiency disease, NOS", "congenital Hageman factor deficiency", "Congenital Hageman factor deficiency", "Factor XII deficiency disease (disorder)", "congenital factor XII deficiency (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital factor XII deficiency", "shortest_name_length": 13}
{"curie": "UMLS:C2981400", "names": ["Stage IIC Colorectal Cancer", "Stage IIC Colorectal Cancer AJCC v7", "Stage IIC Colorectal (Colon or Rectal) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIC Colorectal Cancer AJCC v7", "shortest_name_length": 27}
{"curie": "MONDO:0045051", "names": ["CS", "cortical cataract", "Cortical Cataract", "Cortical cataract", "cataract cortical", "Cataract cortical", "Cataract, cortical", "cataracts cortical", "Cortical Spoking Cataract", "Cataract, zonular cortical", "Cortical cataract (disorder)", "lens cortex cataract (disease)", "cataract (disease) of lens cortex", "cortical cataract (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cortical cataract", "shortest_name_length": 2}
{"curie": "UMLS:C2919522", "names": ["Congenital hemolytic uremic syndrome", "Congenital haemolytic uraemic syndrome", "Congenital hemolytic uremic syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital hemolytic uremic syndrome", "shortest_name_length": 36}
{"curie": "MONDO:0003967", "names": ["synchronous multifocal osteosarcoma", "Synchronous Multifocal Osteosarcoma", "Synchronous Multifocal Osteogenic Sarcoma", "synchronous multifocal osteogenic sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "synchronous multifocal osteogenic sarcoma", "shortest_name_length": 35}
{"curie": "UMLS:C0344911", "names": ["dilated left ventricle", "LEFT VENTRICLE DILATED", "left ventricle dilated", "Dilated left ventricle", "Left ventricle dilated", "left ventricular dilatation", "Left ventricular dilatation", "Left ventricular chamber dilated", "Left cardiac ventricular dilatation", "Dilatation of left cardiac ventricle", "Dilatation of left cardiac ventricle (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Left cardiac ventricular dilatation", "shortest_name_length": 22}
{"curie": "MONDO:0006218", "names": ["Gallbladder BilIN", "Intracystic BilIN", "gallbladder BilIN", "intracystic BilIN", "Gallbladder Dysplasia", "gallbladder dysplasia", "Gallbladder Intraepithelial Neoplasia", "gallbladder intraepithelial neoplasia", "Intracystic Biliary Intraepithelial Neoplasia", "intracystic biliary intraepithelial neoplasia", "Gallbladder Biliary Intraepithelial Neoplasia", "gallbladder biliary intraepithelial neoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gallbladder biliary intraepithelial neoplasia", "shortest_name_length": 17}
{"curie": "UMLS:C1332443", "names": ["BRCA2 Syndrome", "Site Specific Early Onset Breast Cancer Syndrome", "BRCA2-Associated Hereditary Breast and Ovarian Cancer Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "BRCA2-Associated Hereditary Breast and Ovarian Cancer Syndrome", "shortest_name_length": 14}
{"curie": "MONDO:0009755", "names": ["NAD", "Clark Nevus", "Clark's Nevus", "Atypical Nevus", "dysplastic nevi", "dysplastic nevus", "Dysplastic nevus", "dysplastic Nevus", "Dysplastic Nevus", "Lentiginous Nevus", "lentiginous Nevus", "NEUTROPHIL ACTIN DYSFUNCTION", "neutrophil actin dysfunction", "Neutrophil Actin Dysfunction", "Nevus with Architectural Disorder", "Nevus with architectural disorder", "Nevus with Architectural Disorder and Cytologic Atypia of Melanocytes", "Nevus with architectural disorder and cytologic atypia of melanocytes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neutrophil actin dysfunction", "shortest_name_length": 3}
{"curie": "MONDO:0700155", "names": ["canine thyroid adenocarcinoma", "Canine Thyroid Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "canine thyroid adenocarcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0017741", "names": ["disorder of protein O-glycosylation", "protein O-linked glycosylation disease", "disorder of protein O-linked glycosylation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of protein O-glycosylation", "shortest_name_length": 35}
{"curie": "MONDO:0054729", "names": ["SPGF25", "spermatogenic failure 25", "SPERMATOGENIC FAILURE 25"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 25", "shortest_name_length": 6}
{"curie": "OMIM:110450", "names": ["COLTON-NULL PHENOTYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "shortest_name_length": 21}
{"curie": "UMLS:C4054366", "names": ["Nephrotic Syndrome - SMARCAL1 Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - SMARCAL1 Associated", "shortest_name_length": 40}
{"curie": "MONDO:0008587", "names": ["TRACHEOPATHIA OSTEOPLASTICA", "Tracheopathia osteoplastica", "tracheopathia osteoplastica", "Tracheopathia osteochondroplastica", "Tracheobronchopathia osteoplastica", "tracheobronchopathia osteoplastica", "Tracheobroncheopathia osteoplastica", "Tracheopathia osteoplastica (disorder)", "TRACHEOBRONCHOPATHIA OSTEOCHONDROPLASTICA", "Tracheobronchopathia-osteochondroplastica", "tracheobronchopathia osteochondroplastica", "Tracheobronchopathia Osteochondroplastica", "Tracheobronchopathia osteochondroplastica", "Tracheobroncheopathia osteoplastica (disorder)", "cartilaginous or bony projections into the tracheobronchial lumen", "Cartilaginous or bony projections into the tracheobronchial lumen"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tracheobronchopathia osteochondroplastica", "shortest_name_length": 27}
{"curie": "MONDO:0030070", "names": ["HTX9", "heterotaxy, visceral, 9, autosomal, with male infertility", "HETEROTAXY, VISCERAL, 9, AUTOSOMAL, WITH MALE INFERTILITY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heterotaxy, visceral, 9, autosomal, with male infertility", "shortest_name_length": 4}
{"curie": "MONDO:0019736", "names": ["MPGNII", "MPGN 2", "MPGNIIs", "DDD MPGNII", "DDD MPGNIIs", "MPGNII, DDD", "Type II MPGN", "Type II MPGNs", "MPGN, Type II", "Dense deposit disease", "Dense Deposit Disease", "dense deposit disease", "Dense deposit disease (disorder)", "Dense deposit disease (diagnosis)", "Mesangiocapillary Glomerulonephritis Type 2", "Mesangiocapillary glomerulonephritis type 2", "Mesangiocapillary glomerulonephritis type II", "Mesangiocapillary glomerulonephritis, type II", "Mesangiocapillary Glomerulonephritis, Type II", "Membranoproliferative Glomerulonephritis Type 2", "glomerulonephritis membranoproliferative type 2", "membranoproliferative glomerulonephritis type 2", "Membranoproliferative glomerulonephritis type 2", "membranoproliferative glomerulonephritis type II", "Membranoproliferative glomerulonephritis type II", "Membranoproliferative Glomerulonephritis Type II", "Glomerular subendothelial electron-dense deposits", "Membranoproliferative Glomerulonephritis, Type II", "Glomerulonephritis, membranoproliferative, Type II", "MPGNII - membranoproliferative glomerulonephritis type II", "Mesangiocapillary glomerulonephritis, type II (diagnosis)", "MCGN type II - Mesangiocapillary glomerulonephritis type II", "MCGN type II - mesangiocapillary glomerulonephritis type II", "MCGNdd - Mesangiocapillary glomerulonephritis, dense deposit"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dense deposit disease", "shortest_name_length": 6}
{"curie": "UMLS:C0280190", "names": ["Recurrent Immunoblastic Lymphoma", "Relapsed Adult Immunoblastic Lymphoma", "Recurrent Adult Immunoblastic Lymphoma", "relapsed adult immunoblastic large cell lymphoma", "Relapsed Adult Immunoblastic Large Cell Lymphoma", "adult immunoblastic large cell lymphoma, relapsed", "recurrent adult immunoblastic large cell lymphoma", "Recurrent Adult Immunoblastic Large Cell Lymphoma", "adult immunoblastic large cell lymphoma, recurrent", "immunoblastic large cell lymphoma, recurrent, adult", "immunoblastic large cell lymphoma, adult, recurrent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Adult Immunoblastic Lymphoma", "shortest_name_length": 32}
{"curie": "UMLS:C0729587", "names": ["Infective blepharitis", "Infective blepharitis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infective blepharitis", "shortest_name_length": 21}
{"curie": "UMLS:C0338650", "names": ["Organic Catatonia", "Organic Catatonias", "Catatonia, Organic", "Catatonias, Organic", "Organic Catatonic Disorder", "Organic catatonic disorder", "Organic Catatonic Disorders", "organic; catatonic disorder", "Catatonic Disorder, Organic", "catatonic; organic disorder", "organic; disorder, catatonic", "disorder; catatonic, organic", "catatonic; disorder, organic", "disorder; organic, catatonic", "Catatonic Disorders, Organic", "Organic catatonic disorder (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Catatonia, Organic", "shortest_name_length": 17}
{"curie": "UMLS:C2986665", "names": ["Early-Stage Breast Cancer", "early-stage breast cancer", "Early-Stage Breast Carcinoma", "Early Stage Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Early Stage Breast Carcinoma", "shortest_name_length": 25}
{"curie": "MONDO:0002951", "names": ["Adenoid Basal Cell Carcinoma", "adenoid basal cell carcinoma", "Basal cell carcinoma - adenoid", "Skin Adenoid Basal Cell Carcinoma", "skin adenoid basal cell carcinoma", "Basal cell carcinoma - adenoid (disorder)", "Basal cell carcinoma - adenoid (diagnosis)", "malignant neoplasm carcinoma basal cell adenoid"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "skin adenoid basal cell carcinoma", "shortest_name_length": 28}
{"curie": "UMLS:C0281293", "names": ["AIDS-Related Hodgkin Lymphoma", "HIV-Related Hodgkin's Disease", "AIDS-related Hodgkin lymphoma", "AIDS-Related Hodgkin's Disease", "HIV-Related Hodgkin's Lymphoma", "AIDS-related Hodgkin's disease", "AIDS-Related Hodgkin's Lymphoma", "HIV-associated Hodgkin lymphoma", "HIV-associated Hodgkin's disease", "HIV-Associated Hodgkin's Disease", "AIDS-Associated Hodgkin's Disease", "HIV-Associated Hodgkin's Lymphoma", "AIDS-associated Hodgkin's disease", "AIDS-Associated Hodgkin's Lymphoma", "AIDS-associated Hodgkin's lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AIDS-Related Hodgkin Lymphoma", "shortest_name_length": 29}
{"curie": "MONDO:0008695", "names": ["CHAC", "Chac", "ChAc", "Neuroacanthocytosis", "neuroacanthocytosis", "CHOREOACANTHOCYTOSIS", "Choreoacanthocytosis", "choreoacanthocytosis", "choreaacanthocytosis", "Choreoacanthocytoses", "Chorea-Acanthocytoses", "chorea-acanthocytosis", "choreo-acanthocytosis", "Chorea-Acanthocytosis", "CHOREA-ACANTHOCYTOSIS", "Chorea-acanthocytosis", "Chorea Acanthocytosis", "Chorea Acanthocytoses", "chorea acanthocytosis", "Acanthocytosis, Chorea", "Acanthocytoses, Chorea", "Levine-Critchley Syndrome", "Levine-Critchley syndrome", "Levine Critchley Syndrome", "NEUROACANTHOCYTOSIS, FORMERLY", "Chorea acanthocytosis syndrome", "chorea acanthocytosis syndrome", "Chorea Acanthocytosis Syndrome", "Choreoacanthocytosis (disorder)", "Chorea Acanthocytosis Syndromes", "LEVINE-CRITCHLEY SYNDROME, FORMERLY", "Acanthocytosis with Neurologic Disorder", "acanthocytosis with neurologic disorder", "ACANTHOCYTOSIS WITH NEUROLOGIC DISORDER", "Chorea acanthocytosis syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chorea-acanthocytosis", "shortest_name_length": 4}
{"curie": "MONDO:0010131", "names": ["GTHR", "GRTH", "THRB", "Gthr", "GRTHR", "Refetoff syndrome", "REFETOFF SYNDROME", "Thyroid Hormone Resistance", "thyroid hormone resistance", "thyroid hormone receptor BETA", "thyroid hormone unresponsiveness", "THYROID HORMONE UNRESPONSIVENESS", "Thyroid Hormone Resistance Syndrome", "thyroid hormone resistance syndrome", "thyroid hormone resistance, autosomal recessive", "thyroid hormone resistance, generalized, autosomal recessive", "THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL RECESSIVE", "Thyroid Hormone Resistance, Generalized, Autosomal Recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thyroid hormone resistance, generalized, autosomal recessive", "shortest_name_length": 4}
{"curie": "MONDO:0011712", "names": ["VWS2", "VAN DER Woude syndrome 2", "Van der Woude syndrome 2", "van der Woude syndrome 2", "VAN DER WOUDE SYNDROME 2", "GRHL3 van der Woude syndrome", "Van Der Woude syndrome type 2", "van der Woude syndrome caused by mutation in GRHL3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "van der Woude syndrome 2", "shortest_name_length": 4}
{"curie": "MONDO:0002106", "names": ["labyrinthine unilateral reactive loss", "Unilateral loss of labyrinthine reactivity", "unilateral loss of labyrinthine reactivity", "Loss of labyrinthine reactivity, unilateral", "loss of labyrinthine reactivity, unilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "labyrinthine unilateral reactive loss", "shortest_name_length": 37}
{"curie": "MONDO:0035237", "names": ["bullous pyoderma gangrenosum", "Phemphigoid pyoderma gangrenosum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bullous pyoderma gangrenosum", "shortest_name_length": 28}
{"curie": "MONDO:0009089", "names": ["deafness oligodontia syndrome", "deafness-oligodontia syndrome", "Deafness-Oligodontia Syndrome", "DEAFNESS-OLIGODONTIA SYNDROME", "Deafness oligodontia syndrome", "Deafness-oligodontia syndrome", "Deafness and oligodontia syndrome", "Hearing loss-oligodontia syndrome", "Deafness and oligodontia syndrome (disorder)", "congenital profound sensorineural deafness and oligodontia", "Congenital profound sensorineural deafness and oligodontia", "autosomal recessive sensorineural hearing impairment, dizziness, and hypodontia", "Autosomal recessive sensorineural hearing impairment, dizziness, and hypodontia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "deafness-oligodontia syndrome", "shortest_name_length": 29}
{"curie": "UMLS:C5230921", "names": ["Differentiated intraepithelial neoplasia", "Differentiated Intraepithelial Neoplasia", "Differentiated intraepithelial neoplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Differentiated intraepithelial neoplasia", "shortest_name_length": 40}
{"curie": "UMLS:C0302329", "names": ["Germinoblastic sarcoma", "Centroblastic Lymphoma", "lymphoma; centroblastic", "centroblastic; lymphoma", "Diffuse Centroblastic Lymphoma", "diffuse centroblastic lymphoma", "Germinoblastic sarcoma, diffuse", "Malignant lymphoma, centroblastic type", "Malignant lymphoma, centroblastic, NOS", "Malignant lymphoma centroblastic, diffuse", "diffuse centroblastic lymphoma (diagnosis)", "Diffuse malignant lymphoma - centroblastic", "Malignant lymphoma, centroblastic, diffuse", "Diffuse non-Hodgkin's centroblastic lymphoma", "Malignant lymphoma, centroblastic type, diffuse", "Diffuse malignant lymphoma - centroblastic (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant lymphoma centroblastic, diffuse", "shortest_name_length": 22}
{"curie": "MONDO:0019220", "names": ["disorder of cobalamin metabolism and transport", "inborn disorder of cobalamin metabolism and transport"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of cobalamin metabolism and transport", "shortest_name_length": 46}
{"curie": "MONDO:0024343", "names": ["scurf", "Scurf", "Dandruff", "dandruff", "furfuracea", "Scurfiness of skin", "Pityriasis simplex", "pityriasis simplex", "Scurfiness of scalp", "Pityriasis simplex (disorder)", "pityriasis simplex (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pityriasis simplex", "shortest_name_length": 5}
{"curie": "MONDO:0000373", "names": ["gallbladder carcinoma in situ", "gall bladder carcinoma in situ", "gall bladder in situ carcinoma", "stage 0 gall bladder carcinoma", "carcinoma in situ of gall bladder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gall bladder carcinoma in situ", "shortest_name_length": 29}
{"curie": "MONDO:0060774", "names": ["Vaginal Fibroepithelial Polyp", "VAGINAL FIBROEPITHELIAL POLYP", "vaginal fibroepithelial polyp", "Fibroepithelial Polyp of Vagina", "fibroepithelial polyp of vagina", "fibroepithelial polyp of the vagina", "Fibroepithelial Polyp of the Vagina", "Vaginal Fibroepithelial Stromal Polyp", "vaginal fibroepithelial stromal polyp"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vaginal fibroepithelial polyp", "shortest_name_length": 29}
{"curie": "MONDO:0012912", "names": ["PPHP", "AHO-PPHP syndrome", "aho-PPHP syndrome", "Pseudopseudohypoparathyroidism", "pseudopseudohypoparathyroidism", "PSEUDOPSEUDOHYPOPARATHYROIDISM", "Pseudopseudohypoparathyroidisms", "Pseudo-Pseudohypoparathyroidism", "Pseudo Pseudohypoparathyroidism", "Pseudo-pseudohypoparathyroidism", "pseudo-pseudohypoparathyroidism", "Pseudopseudo-hypoparathyroidism", "Pseudopseudo Hypoparathyroidism", "Pseudopseudo-Hypoparathyroidism", "pseudo pseudo hypoparathyroidism", "Pseudo-Pseudohypoparathyroidisms", "Pseudopseudo-Hypoparathyroidisms", "pseudopseudohypoparathyroidism (PPHP)", "Normocalcemic pseudohypoparathyroidism", "Pseudopseudohypoparathyroidism (disorder)", "Albright hereditary osteodystrophy type 2", "pseudopseudohypoparathyroidism (diagnosis)", "Albright hereditary osteodystrophy-PPHP syndrome", "Normocalcemic pseudohypoparathyroidism (disorder) [ambiguous]", "Albright Hereditary osteodystrophy with multiple hormone resistance", "Albright Hereditary Osteodystrophy with Multiple Hormone Resistance", "Albright hereditary osteodystrophy without multiple hormone resistance", "ALBRIGHT HEREDITARY OSTEODYSTROPHY WITHOUT MULTIPLE HORMONE RESISTANCE", "Albright Hereditary Osteodystrophy without Multiple Hormone Resistance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudopseudohypoparathyroidism", "shortest_name_length": 4}
{"curie": "MONDO:0015811", "names": ["Berti lymphoma", "Primary cutaneous epidermotropic cytotoxic CD8+ T-cell lymphoma", "primary cutaneous epidermotropic cytotoxic CD8+ T-cell lymphoma", "Primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma", "primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma", "Primary cutaneous epidermotropic cytotoxic CD8 positive T-cell lymphoma", "Primary Cutaneous CD8-Positive Aggressive Epidermotropic T-Cell Lymphoma", "Primary Cutaneous Aggressive Epidermotropic CD8-Positive T-Cell Lymphoma", "Primary Cutaneous CD8-Positive Aggressive Epidermotropic Cytotoxic T-Cell Lymphoma", "Primary cutaneous CD8 positive aggressive epidermotropic cytotoxic T-cell lymphoma", "Primary cutaneous CD8-positive aggressive epidermotropic cytotoxic T-cell lymphoma", "Primary cutaneous CD8 positive aggressive epidermotropic cytotoxic T-cell lymphoma (disorder)", "Primary cutaneous CD8 positive aggressive epidermotropic cytotoxic T-cell lymphoma (diagnosis)", "Primary cutaneous CD8 positive aggressive epidermotropic cytotoxic T-cell lymphoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma", "shortest_name_length": 14}
{"curie": "MONDO:0011632", "names": ["MSP5", "ALS21", "MPD2, FORMERLY", "VCPDM, FORMERLY", "myopathy, distal, 2", "MULTISYSTEM PROTEINOPATHY 5", "MYOPATHY, DISTAL, 2, FORMERLY", "myopathy, distal, 2, formerly", "Amyotrophic Lateral Sclerosis 21", "AMYOTROPHIC LATERAL SCLEROSIS 21", "amyotrophic lateral sclerosis 21", "MATR3 amyotrophic lateral sclerosis", "amyotrophic lateral sclerosis type 21", "amyotrophic lateral sclerosis caused by mutation in MATR3", "vocal cord and pharyngeal dysfunction with distal myopathy", "VOCAL CORD AND PHARYNGEAL DYSFUNCTION WITH DISTAL MYOPATHY, FORMERLY", "vocal cord and pharyngeal dysfunction with distal myopathy, formerly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "amyotrophic lateral sclerosis type 21", "shortest_name_length": 4}
{"curie": "UMLS:C0231557", "names": ["abnormal ossification", "Abnormal ossification", "Ossification, abnormal", "Abnormal bone formation", "Bone formation, abnormal", "abnormal bones formation", "BONE DEVELOPMENT ABNORMAL", "Abnormal Bone Development", "Bone development abnormal", "Abnormal bone formation (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Abnormal bone formation", "shortest_name_length": 21}
{"curie": "UMLS:C0155970", "names": ["perforation; gastric ulcer, acute", "Acute gastric ulcer with perforation", "acute gastric ulcer with perforation", "Gastric ulcer, acute with perforation", "Gastric ulcer acute, with perforation", "ulcer; gastric, acute, with perforation", "stomach; ulcer, acute, with perforation", "Acute gastric ulcer with perforation (disorder)", "acute gastric ulcer with perforation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Acute gastric ulcer with perforation", "shortest_name_length": 33}
{"curie": "UMLS:C2584620", "names": ["Primary thrombophilia", "thrombophilia primary", "Hereditary thrombophilia", "Thrombophilia, hereditary", "thrombophilia primary (diagnosis)", "Hereditary hypercoagulable disorder", "Hereditary thrombophilia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Thrombophilia, hereditary", "shortest_name_length": 21}
{"curie": "UMLS:C1336381", "names": ["Stage IVB Mouth Adenoid Cystic Carcinoma", "Stage IVB Adenoid Cystic Carcinoma of Mouth", "Stage IVB Oral Cavity Adenoid Cystic Cancer", "Stage IVB Oral Cavity Adenoid Cystic Carcinoma", "Stage IVB Adenoid Cystic Carcinoma of the Mouth", "Stage IVB Adenoid Cystic Carcinoma of Oral Cavity", "Stage IVB Adenoid Cystic Carcinoma of the Oral Cavity", "Stage IVB Oral Cavity Adenoid Cystic Carcinoma AJCC v6", "Stage IVB Oral Cavity Adenoid Cystic Carcinoma AJCC v7", "Stage IVB Oral Cavity Adenoid Cystic Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Oral Cavity Adenoid Cystic Carcinoma AJCC v6 and v7", "shortest_name_length": 40}
{"curie": "UMLS:C1699201", "names": ["Infusion site thrombophlebitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infusion site thrombophlebitis", "shortest_name_length": 30}
{"curie": "MONDO:0013791", "names": ["THPH6", "thrombophilia due to PROTEIN S deficiency, autosomal recessive", "THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL RECESSIVE", "thrombophilia due to protein S deficiency, autosomal recessive", "thrombophilia 5 due to protein S deficiency, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombophilia due to protein S deficiency, autosomal recessive", "shortest_name_length": 5}
{"curie": "MONDO:0009760", "names": ["LIS2", "Lissencephaly 2", "LISSENCEPHALY 2", "lissencephaly 2", "Norman-Roberts syndrome", "NORMAN-ROBERTS SYNDROME", "Microlissencephaly type A", "Norman-Roberts syndrome (NRS)", "Norman-Roberts lissencephaly syndrome", "lissencephaly 2 (Norman-Roberts type)", "Norman Roberts lissencephaly syndrome", "lissencephaly syndrome Norman-Roberts type", "Lissencephaly syndrome Norman Roberts type", "Lissencephaly syndrome, Norman-Roberts type", "lissencephaly syndrome, Norman-Roberts type", "LISSENCEPHALY SYNDROME, NORMAN-ROBERTS TYPE", "Lissencephaly syndrome Norman Roberts type (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Norman-Roberts syndrome", "shortest_name_length": 4}
{"curie": "MONDO:0011582", "names": ["Mmds", "MMDS", "MMDS1", "NFU1 deficiency", "MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1", "multiple mitochondrial dysfunctions syndrome 1", "Multiple mitochondrial dysfunctions syndrome type 1", "multiple mitochondrial dysfunctions syndrome type 1", "NFU1 (NFU1 iron-sulfur cluster scaffold) deficiency", "NFU1 fatal multiple mitochondrial dysfunctions syndrome", "MMDS1 - multiple mitochondrial dysfunctions syndrome type 1", "Multiple mitochondrial dysfunctions syndrome type 1 (disorder)", "fatal multiple mitochondrial dysfunctions syndrome caused by mutation in NFU1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple mitochondrial dysfunctions syndrome 1", "shortest_name_length": 4}
{"curie": "UMLS:C2981720", "names": ["stage IVA mycosis fungoides/Sezary syndrome", "Stage IVA Mycosis Fungoides and Sézary Syndrome", "Stage IVA Mycosis Fungoides and Sezary Syndrome", "Stage IVA Mycosis Fungoides and Sézary Syndrome AJCC v7", "stage IVA mycosis fungoides and Sezary syndrome AJCC v7", "Stage IVA Mycosis Fungoides and Sezary Syndrome AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Mycosis Fungoides and Sezary Syndrome AJCC v7", "shortest_name_length": 43}
{"curie": "UMLS:C0948765", "names": ["Cyclosporine toxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cyclosporine toxicity", "shortest_name_length": 21}
{"curie": "MONDO:0019340", "names": ["scleroderma", "Scleroderma", "SCLERODERMA", "sclerodermas", "Dermatosclerosis", "dermatosclerosis", "Pseudoscleroderma", "scleroderma disease", "disease scleroderma", "Scleroderma (Disease)", "scleroderma (disease)", "scleroderma (diagnosis)", "Progressive systemic scleroderma", "Scleroderma-like secondary cutaneous sclerosis", "Scleroderma-like secondary cutaneous sclerosis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "scleroderma", "shortest_name_length": 11}
{"curie": "MONDO:0001750", "names": ["non-renal secondary hyperparathyroidism", "Secondary hyperparathyroidism, non-renal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "non-renal secondary hyperparathyroidism", "shortest_name_length": 39}
{"curie": "MONDO:0019139", "names": ["acquired hemophilia", "Acquired hemophilia", "acquired haemophilia", "Acquired haemophilia", "hemophilia, acquired", "Acquired hemophilia (disorder)", "acquired hemophilia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired hemophilia", "shortest_name_length": 19}
{"curie": "MONDO:0001022", "names": ["Disuse amblyopia", "disuse amblyopia", "Amblyopia ex anopsia", "amblyopia ex anopsia", "ex anopsia; amblyopia", "amblyopia; ex anopsia", "deprivation amblyopia", "Deprivation amblyopia", "Amblyopia, deprivation", "Stimulus deprivation amblyopia", "amblyopia ex anopsia (diagnosis)", "deprivation amblyopia (diagnosis)", "Stimulus deprivation amblyopia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disuse amblyopia", "shortest_name_length": 16}
{"curie": "MONDO:0014996", "names": ["MRT58", "ELP2-related disorder", "MENTAL RETARDATION, AUTOSOMAL RECESSIVE 58", "mental retardation, autosomal recessive 58", "autosomal recessive intellectual disability 58", "intellectual disability, autosomal recessive 58", "mental retardation, autosomal recessive type 58", "intellectual disability, autosomal recessive type 58", "autosomal recessive intellectual developmental disorder 58", "intellectual developmental disorder, autosomal recessive 58", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 58", "ELP2 autosomal recessive non-syndromic intellectual disability", "autosomal recessive non-syndromic intellectual disability caused by mutation in ELP2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal recessive 58", "shortest_name_length": 5}
{"curie": "UMLS:C5556792", "names": ["Advanced Vaginal Adenosquamous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Vaginal Adenosquamous Carcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0032686", "names": ["SPGF35", "spermatogenic failure 35", "SPERMATOGENIC FAILURE 35"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 35", "shortest_name_length": 6}
{"curie": "MONDO:0017302", "names": ["qualitative or quantitative defects of troponin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of troponin", "shortest_name_length": 47}
{"curie": "MONDO:0011580", "names": ["CEREBELLAR ATAXIA AND HYPERGONADOTROPIC HYPOGONADISM", "Cerebellar Ataxia and Hypergonadotropic Hypogonadism", "cerebellar ataxia and hypergonadotropic hypogonadism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cerebellar ataxia and hypergonadotropic hypogonadism", "shortest_name_length": 52}
{"curie": "UMLS:C0015401", "names": ["eye foreign body", "body eye foreign", "EYE FOREIGN BODY", "foreign body eye", "Eye Foreign Body", "foreign eye body", "Foreign Body, Eye", "Eye Foreign Bodies", "eye foreign bodies", "Eye Foreign Object", "Eye foreign bodies", "foreign body of eye", "Eye--Foreign bodies", "FOREIGN BODY IN EYE", "Foreign body in eye", "foreign body in eye", "Foreign Bodies, Eye", "Eye Foreign Objects", "Foreign Object, Eye", "Foreign Objects, Eye", "Foreign body (in);eye", "foreign body; eyeball", "Foreign body in eyeball", "Intraocular foreign body", "intraocular foreign body", "Intraocular Foreign Body", "foreign body; intraocular", "intraocular; foreign body", "bodies foreign intraocular", "Foreign body retained in eye", "Retained foreign body in eye", "Foreign body in eye (disorder)", "foreign body of eye (diagnosis)", "IOFB - Intraocular foreign body", "Retained foreign body in eye, NOS", "Retained intraocular foreign body", "intraocular foreign body (diagnosis)", "Foreign body, intraocular, unspecified", "Retained intraocular foreign body, NOS", "Retained foreign body in eye (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Eye foreign bodies", "shortest_name_length": 16}
{"curie": "MONDO:0004491", "names": ["choriocarcinoma", "uterine corpus choriocarcinoma", "Uterine Corpus Choriocarcinoma", "body of uterus choriocarcinoma (disease)", "Uterine Corpus Gestational Choriocarcinoma", "Gestational Uterine Corpus Choriocarcinoma", "uterine corpus gestational choriocarcinoma", "gestational uterine corpus choriocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine corpus choriocarcinoma", "shortest_name_length": 15}
{"curie": "UMLS:C0080194", "names": ["Strain", "strain", "strains", "Strains", "strained", "Strain, NOS", "pull muscle", "muscle pull", "muscles pull", "muscle pulls", "Pulled muscle", "pulled muscle", "Muscle strain", "strain muscle", "Muscle Strain", "muscle strain", "muscle pulled", "MUSCLE STRAIN", "muscle pulling", "strain; muscle", "muscle; strain", "muscles strain", "muscles pulled", "muscle strains", "muscles strains", "muscle strained", "muscles pulling", "Strain;muscle(s)", "muscles strained", "strain (diagnosis)", "muscle pull or tear", "Muscle strain (disorder)", "strain of unspecified muscle", "strain of unspecified muscle (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Muscle strain", "shortest_name_length": 6}
{"curie": "MONDO:0019752", "names": ["pediatric Castleman disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pediatric Castleman disease", "shortest_name_length": 27}
{"curie": "MONDO:0006953", "names": ["isoimmunisation rh", "rh isoimmunisation", "RH ISOIMMUNIZATION", "rh isoimmunization", "isoimmunization rh", "Rh isoimmunization", "Rh Isoimmunization", "Rh isoimmunisation", "Rh Isoimmunizations", "Isoimmunization, Rh", "RH iso-immunization", "RH iso-immunisation", "RH;iso-immunisation", "Isoimmunizations, Rh", "Rhesus isoimmunization", "rhesus isoimmunization", "rhesus isoimmunisation", "Rhesus isoimmunisation", "Rhesus Isoimmunization", "Isoimmunization, Rhesus", "Rhesus Isoimmunizations", "Isoimmunizations, Rhesus", "RI - Rhesus isoimmunization", "RI - Rhesus isoimmunisation", "pregnancy; isoimmunization, rhesus", "Rhesus isoimmunization in pregnancy", "Rhesus isoimmunisation in pregnancy", "Rh incompatibility affecting pregnancy", "Rhesus isoimmunization affecting pregnancy", "Rhesus isoimmunisation affecting pregnancy", "Rh isoimmunization affecting care of mother", "Rh antibodies affecting management of mother", "Rh incompatibility affecting management of mother", "Rhesus isoimmunization affecting pregnancy (disorder)", "Rh isoimmunization affecting care of mother (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Rh isoimmunization", "shortest_name_length": 18}
{"curie": "MONDO:0001210", "names": ["Sunken eye", "Eye sunken", "sunken eye", "eyes sunken", "sunken eyes", "Enopthalmos", "SUNKEN EYES", "Eyes sunken", "Sunken eyes", "enophthalmos", "ENOPHTHALMOS", "Deep set eye", "enophthalmia", "Enophthalmia", "Enophthalmos", "Deep set eyes", "deep set eyes", "Deep-set eyes", "Deeply set eye", "Deeply set eyes", "Ocular depression", "Enophthalmos, NOS", "Sunken eyes (finding)", "enophthalmos (disease)", "Enophthalmos (disorder)", "Unspecified enophthalmos", "enophthalmos (diagnosis)", "enophthalmos was observed", "enophthalmos (physical finding)", "deep set eyes (physical finding)", "Enophthalmos, unspecified as to cause"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "enophthalmos", "shortest_name_length": 10}
{"curie": "MONDO:0030619", "names": ["RP92", "retinitis pigmentosa 92", "RETINITIS PIGMENTOSA 92"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinitis pigmentosa 92", "shortest_name_length": 4}
{"curie": "MONDO:0005874", "names": ["Neuroschistosomiases", "neuroschistosomiasis", "Neuroschistosomiasis", "Central Nervous System Schistosomiasis", "Schistosomiasis, Central Nervous System", "Infection of nervous system caused by Schistosoma", "Infection of nervous system caused by Schistosoma (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuroschistosomiasis", "shortest_name_length": 20}
{"curie": "UMLS:C5555681", "names": ["Metastatic Acral Lentiginous Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Acral Lentiginous Melanoma", "shortest_name_length": 37}
{"curie": "MONDO:0019218", "names": ["disorder of bile acid synthesis", "inborn errors of bile acid synthesis", "inborn disorder of bile acid synthesis", "inborn error of bile acid biosynthetic process", "inborn bile acid biosynthetic process disorder", "rare inborn error of bile acid biosynthetic process"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inborn disorder of bile acid synthesis", "shortest_name_length": 31}
{"curie": "MONDO:0011786", "names": ["ALRH", "Alrh", "Hayfever", "Hay fever", "hay fever", "pollenosis", "nasal allergy", "Nasal allergy", "allergy nasal", "Allergy;nasal", "nasal; allergy", "allergy; nasal", "Rhinallergosis", "Nasal allergies", "Atopic rhinitis", "Atopic Rhinitis", "atopic rhinitis", "allergies nasal", "RHINITIS, ATOPIC", "Allergic Rhinitis", "allergic rhinitis", "ALLERGIC RHINITIS", "RHINITIS ALLERGIC", "Rhinitis;allergic", "Allergic rhinitis", "Rhinitis allergic", "allergic; rhinitis", "RHINITIS, ALLERGIC", "rhinitis; allergic", "Rhinitis, Allergic", "Allergic Rhinitides", "Rhinitides, Allergic", "Rhinitis allergic NOS", "AR - Allergic rhinitis", "Allergic rhinitis, NOS", "Allergic rhinosinusitis", "allergic rhinosinusitis", "RHINITIS ALLERGIC ATOPIC", "Rhinitis allergic atopic", "allergic form of rhinitis", "seasonal allergic rhinitis", "Perenial allergic rhinitis", "perennial allergic rhinitis", "Allergic rhinitis (disorder)", "allergic rhinitis (diagnosis)", "Non-seasonal allergic rhinitis", "non-seasonal allergic rhinitis", "Allergic rhinitis, unspecified", "Allergic rhinitis due to allergen", "Allergic rhinitis, cause unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "allergic rhinitis", "shortest_name_length": 4}
{"curie": "UMLS:C3899656", "names": ["Pediatric Infectious Disease", "Pediatric Infectious Disorder", "Pediatric infectious diseases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pediatric Infectious Disorder", "shortest_name_length": 28}
{"curie": "MONDO:0011646", "names": ["laryngeal abductor paralysis with cerebellar ataxia and motor neuropathy", "Laryngeal Abductor Paralysis with Cerebellar Ataxia and Motor Neuropathy", "LARYNGEAL ABDUCTOR PARALYSIS WITH CEREBELLAR ATAXIA AND MOTOR NEUROPATHY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laryngeal abductor paralysis with cerebellar ataxia and motor neuropathy", "shortest_name_length": 72}
{"curie": "MONDO:0008477", "names": ["SMDK", "SmD Kozlowski type", "SMD Kozlowski type", "SMD, KOZLOWSKI TYPE", "SmD, Kozlowski type", "SMD, Kozlowski Type", "Jequier-Kozlowski syndrome", "Jequier Kozlowski skeletal dysplasia", "Kozlowski spondylometaphyseal dysplasia", "skeletal dysplasia Jequier-Kozlowski type", "Spondylometaphyseal dysplasia Kozlowski type", "spondylometaphyseal dysplasia Kozlowski type", "spondylometaphyseal dysplasia, Kozlowski type", "SPONDYLOMETAPHYSEAL DYSPLASIA, KOZLOWSKI TYPE", "Spondylometaphyseal dysplasia, Kozlowski type", "Spondylometaphyseal dysplasia - Kozlowski type", "Kozlowski's spondylometaphyseal dysplasia syndrome", "Kozlowski spondylometaphyseal dysplasia (disorder)", "dysmorphism arthrogryposis skeletal maturation advanced", "Dysmorphism arthrogryposis skeletal maturation advanced"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondylometaphyseal dysplasia, Kozlowski type", "shortest_name_length": 4}
{"curie": "MONDO:0004499", "names": ["Lung Hilum Cancer", "lung hilum cancer", "hilar lung carcinoma", "Hilar Lung Carcinoma", "lung hilus carcinoma", "Lung Hilum Carcinoma", "lung hilum carcinoma", "carcinoma of lung hilus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung hilum carcinoma", "shortest_name_length": 17}
{"curie": "MONDO:0009698", "names": ["Uld", "PME", "ULD", "EPM1", "EPM1A", "PME type 1", "Unverricht", "Baltic Myoclonus", "Myoclonus, Baltic", "Unverricht Disease", "Disease, Unverricht", "Unverricht Diseases", "UNVERRICHT SYNDROME", "Diseases, Unverricht", "epilepsy; Unverricht", "Unverricht's disease", "Unverricht's syndrome", "Unverricht; epileptic", "Baltic Myoclonic Epilepsy", "Unverricht-Lafora disease", "Baltic myoclonic epilepsy", "Baltic myoclonus epilepsy", "BALTIC MYOCLONIC EPILEPSY", "baltic myoclonic epilepsy", "Baltic Myoclonus Epilepsy", "Myoclonic Epilepsy, Baltic", "Epilepsy, Baltic Myoclonus", "Epilepsy, Baltic Myoclonic", "Myoclonus Epilepsy, Baltic", "Unverricht-Lundborg disease", "LUNDBORG-UNVERRICHT DISEASE", "Unverricht Lundborg Disease", "Baltic Myoclonus Epilepsies", "unverricht-lundborg disease", "unverricht lundborg disease", "Baltic Myoclonic Epilepsies", "Unverricht-Lundborg Disease", "Lundborg Unverricht Syndrome", "Unverricht-Lundborg Syndrome", "Lundborg-Unverricht Syndrome", "lundborg-unverricht syndrome", "Unverricht-Lundborg Diseases", "Myoclonus Epilepsies, Baltic", "Myoclonic Epilepsies, Baltic", "Epilepsies, Baltic Myoclonus", "Unverricht-Lundborg syndrome", "Unverricht Lundborg Syndrome", "Disease, Unverricht-Lundborg", "Epilepsies, Baltic Myoclonic", "Diseases, Unverricht-Lundborg", "Syndrome, Lundborg-Unverricht", "Syndrome, Unverricht-Lundborg", "Unverricht - Lundborg disease", "PROGRESSIVE MYOCLONIC EPILEPSY", "progressive myoclonic epilepsy", "Mediterranean Myoclonic Epilepsy", "Progressive Myoclonus Epilepsy 1", "Epilepsy, Progressive Myoclonic 1", "Epilepsy, Mediterranean Myoclonic", "Epilepsy, Progressive Myoclonus 1", "epilepsy, progressive myoclonus 1", "progressive myoclonus epilepsy 1A", "Myoclonic Epilepsy, Mediterranean", "UNVERRICHT-LUNDBORG-LAFORA DISEASE", "EPILEPSY, PROGRESSIVE MYOCLONIC, 1", "epilepsy, progressive myoclonic, 1", "Epilepsy, Progressive Myoclonic 1a", "Epilepsy, Progressive, Myoclonic 1A", "EPILEPSY, PROGRESSIVE MYOCLONIC, 1A", "epilepsy, progressive myoclonic, 1A", "progressive myoclonic epilepsy type 1", "progressive myoclonus epilepsy type 1", "Progressive myoclonus epilepsy type 1", "Progressive myoclonic epilepsy type 1", "epilepsy, progressive myoclonic type 1", "Epilepsy, Progressive Myoclonic Type 1", "Unverricht-Lundborg syndrome (disorder)", "Unverricht-Lundborg syndrome (diagnosis)", "myoclonic epilepsy of Unverricht and Lundborg", "MYOCLONIC EPILEPSY OF UNVERRICHT AND LUNDBORG", "Myoclonic Epilepsy of Unverricht and Lundborg", "Progressive Myoclonus Epilepsybaltic Myoclonic Epilepsy", "progressive myoclonus epilepsy Baltic myoclonic epilepsy", "Myoclonus Progressive Epilepsy of Unverricht and Lundborg", "myoclonus progressive epilepsy of Unverricht and Lundborg", "epilepsy, progressive myoclonic 1A (Unverricht and Lundborg)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unverricht-Lundborg syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0025082", "names": ["Animal Helminthiasis", "animal helminthiasis", "animal Helminthiases", "Animal Helminthiases", "Helminthiases, animal", "Helminthiases, Animal", "Helminthiasis, Animal", "helminthiasis, animal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "helminthiasis, animal", "shortest_name_length": 20}
{"curie": "UMLS:C4331268", "names": ["SUR1-Associated Diabetes Mellitus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "SUR1-Associated Diabetes Mellitus", "shortest_name_length": 33}
{"curie": "UMLS:C1868711", "names": ["Mechanical Ventilation Complication", "Mechanical ventilation complication"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mechanical ventilation complication", "shortest_name_length": 35}
{"curie": "MONDO:0008594", "names": ["FMDF", "Familial multiple trichodiscoma", "Familial multiple trichodiscomas", "familial multiple trichodiscomas", "Trichodiscomas, Familial Multiple", "trichodiscomas, familial multiple", "TRICHODISCOMAS, FAMILIAL MULTIPLE", "Familial multiple discoid fibroma", "Familial multiple discoid fibromas", "hereditary multiple trichodiscomas", "Hereditary multiple trichodiscomas", "familial multiple discoid fibromas", "DISCOID FIBROMAS, FAMILIAL MULTIPLE", "discoid fibromas, familial multiple", "Familial multiple discoid fibroma (disorder)", "small benign fibrovascular tumor of the dermal part of the hair disk"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "familial multiple discoid fibromas", "shortest_name_length": 4}
{"curie": "MONDO:0019289", "names": ["MELANODERMA", "Melanoderma", "melanoderma", "melanodermia", "Melanodermia", "Hypermelanoses", "Hypermelanosis", "hypermelanosis", "hyperpigmentation", "Hyperpigmentation", "HYPERPIGMENTATION", "Hyperpigmented skin", "Patchy darkened skin", "Hyperpigmented lesion", "SKIN HYPERPIGMENTATION", "Hyperpigmentation skin", "Skin Hyperpigmentation", "HYPERPIGMENTATION SKIN", "Skin hyperpigmentation", "Melanoderma (disorder)", "Hyperpigmentation, NOS", "skin hyperpigmentation", "melanoderma (diagnosis)", "Dermal hyperpigmentation", "hyperpigmentation of skin", "Hyperpigmentation of skin", "Hyperpigmentation disorder", "SKIN PIGMENTATION INCREASE", "skin disorders melanoderma", "Cutaneous hyperpigmentation", "Hyperpigmentation disorders", "Increased skin pigmentation", "hyperpigmentation of the skin", "Hyperpigmentation of the skin", "Hyperpigmentation of skin, NOS", "melanoderma (physical finding)", "Hyperpigmentation of skin (disorder)", "Hyperpigmentation (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperpigmentation of the skin", "shortest_name_length": 11}
{"curie": "MONDO:0003575", "names": ["comedocarcinoma", "Comedocarcinoma", "comedo carcinoma", "Comedocarcinoma NOS", "Comedocarcinoma, NOS", "Comedocarcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "comedocarcinoma", "shortest_name_length": 15}
{"curie": "UMLS:C2982437", "names": ["Stage II Nasopharynx Carcinoma", "Stage II Nasopharyngeal Carcinoma", "Stage II Carcinoma of Nasopharynx", "Stage II Carcinoma of the Nasopharynx", "Stage II Nasopharyngeal Throat Cancer", "Stage II Nasopharyngeal Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage II Nasopharyngeal Carcinoma AJCC v7", "shortest_name_length": 30}
{"curie": "MONDO:0017874", "names": ["Junin", "Gripon", "gripon", "Junin; fever", "fever; Junin", "Argentine fever", "Mal de Rastrojos", "O'Higgins' disease", "Junin virus infection", "Junin hemorrhagic fever", "Junin haemorrhagic fever", "hemorrhagic fever; Junin", "Junin; hemorrhagic fever", "Argentine hemorrhagic fever", "argentine hemorrhagic fever", "Hemorrhagic fever, Argentine", "Argentine haemorrhagic fever", "Argentinian hemorrhagic fever", "Argentinian Hemorrhagic Fever", "fever; Argentinian hemorrhagic", "Hemorrhagic fever, Junin virus", "Argentinian haemorrhagic fever", "Argentinian; hemorrhagic fever", "Fever, Argentinian Hemorrhagic", "HEMORRHAGIC FEVER, ARGENTINIAN", "Argentinian hemorrhagic; fever", "hemorrhagic fever; Argentinian", "Hemorrhagic Fever, Argentinian", "Infection caused by Junin virus", "virus; Junin, hemorrhagic fever", "Endoepidemic hemorrhagic viremia", "Endoepidemic haemorrhagic viraemia", "Viral hemorrhagic fever, Argentine", "AHF - Argentinian hemorrhagic fever", "Viral haemorrhagic fever, Argentine", "AHF - Argentinian haemorrhagic fever", "Hemorrhagic fever due to Junin virus", "Haemorrhagic fever due to Junin virus", "Argentine hemorrhagic fever (diagnosis)", "Argentinian hemorrhagic fever (disorder)", "Infection caused by Junin virus (disorder)", "North-east Buenos Aires hemorrhagic viremia", "North-east Buenos Aires haemorrhagic viraemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Argentine hemorrhagic fever", "shortest_name_length": 5}
{"curie": "MONDO:0015791", "names": ["GIPP", "precocious pseudopuberty", "Precocious pseudopuberty", "Pseudoprecocious Puberty", "Peripheral Precocious Puberty", "peripheral precocious puberty", "Peripheral precocious puberty", "Peripheral precocious puberty (disorder)", "Gonadotropin independent precocious puberty", "gonadotropin independent precocious puberty", "Gonadotropin-Independent Precocious Puberty", "gonadotropin-independent precocious puberty", "Precocious puberty, gonadotropin-independent"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "peripheral precocious puberty", "shortest_name_length": 4}
{"curie": "MONDO:0014623", "names": ["MCPH14", "primary autosomal recessive microcephaly 14", "MICROCEPHALY 14, PRIMARY, AUTOSOMAL RECESSIVE", "microcephaly 14, primary, autosomal recessive", "SASS6 autosomal recessive primary microcephaly", "autosomal recessive primary microcephaly caused by mutation in SASS6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly 14, primary, autosomal recessive", "shortest_name_length": 6}
{"curie": "MONDO:0002987", "names": ["Spongiotic Dermatitis", "DERMATITIS SPONGIOTIC", "spongiotic dermatitis", "Spongiotic dermatitis", "Spongiotic dermatitis (disorder)", "spongiotic dermatitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spongiotic dermatitis", "shortest_name_length": 21}
{"curie": "UMLS:C5238499", "names": ["Skin Myoepithelioma", "Cutaneous Myoepithelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin Myoepithelioma", "shortest_name_length": 19}
{"curie": "MONDO:0010891", "names": ["water-West syndrome", "lethal hemolytic anemia-genital anomalies syndrome", "hemolytic anemia lethal congenital nonspherocytic with genital and other abnormalities", "HEMOLYTIC ANEMIA, LETHAL CONGENITAL NONSPHEROCYTIC, WITH GENITAL AND OTHER ABNORMALITIES", "Hemolytic Anemia, Lethal Congenital Nonspherocytic, with Genital and Other Abnormalities", "hemolytic anemia, lethal congenital nonspherocytic, with genital and other abnormalities"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lethal hemolytic anemia-genital anomalies syndrome", "shortest_name_length": 19}
{"curie": "MONDO:0018849", "names": ["DI", "DGI", "DGI without OI", "non-syndromic DGI", "Non-syndromic DGI", "Dentinogenesis imperfecta", "Dentinogenesis Imperfecta", "dentinogenesis imperfecta", "Opalescent teeth without OI", "opalescent teeth without OI", "Hereditary opalescent dentin", "dentinogenesis imperfecta (disease)", "Dentinogenesis imperfecta (disorder)", "dentinogenesis imperfecta (diagnosis)", "non-syndromic dentinogenesis imperfecta", "Non-syndromic dentinogenesis imperfecta", "opalescent teeth without osteogenesis imperfecta", "Opalescent teeth without osteogenesis imperfecta", "Dentinogenesis imperfecta without osteogenesis imperfecta", "dentinogenesis imperfecta without osteogenesis imperfecta"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dentinogenesis imperfecta", "shortest_name_length": 2}
{"curie": "UMLS:C1720498", "names": ["AIDS associated disorder - toxoplasmosis", "Toxoplasmosis associated with acquired immunodeficiency syndrome", "Toxoplasmosis associated with acquired immunodeficiency syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Toxoplasmosis associated with acquired immunodeficiency syndrome", "shortest_name_length": 40}
{"curie": "MONDO:0001237", "names": ["Appendix Lymphoma", "appendix lymphoma", "lymphoma of appendix", "Appendiceal Lymphoma", "Lymphoma of appendix", "Lymphoma of Appendix", "appendiceal lymphoma", "lymphoma of the appendix", "Lymphoma of the Appendix", "primary appendix lymphoma", "Primary Appendix Lymphoma", "vermiform appendix lymphoma", "lymphoma of vermiform appendix", "Lymphoma of appendix (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "appendix lymphoma", "shortest_name_length": 17}
{"curie": "UMLS:C2732697", "names": ["autoimmune myositis", "Autoimmune myositis", "autoimmune myositis (diagnosis)", "Autoimmune inflammation of skeletal muscle", "Autoimmune inflammation of skeletal muscle (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Autoimmune inflammation of skeletal muscle", "shortest_name_length": 19}
{"curie": "MONDO:0033091", "names": ["ARCI14", "autosomal recessive congenital ichthyosis 14", "ichthyosis, congenital, autosomal recessive 14", "ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ichthyosis, congenital, autosomal recessive 14", "shortest_name_length": 6}
{"curie": "UMLS:C4727069", "names": ["Advanced renal cell carcinoma", "Advanced Renal Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced renal cell carcinoma", "shortest_name_length": 29}
{"curie": "MONDO:0017828", "names": ["primary renal tubular acidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary renal tubular acidosis", "shortest_name_length": 30}
{"curie": "UMLS:C1335009", "names": ["Non-Neoplastic Eye Disease", "Non-Neoplastic Eye Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Neoplastic Eye Disorder", "shortest_name_length": 26}
{"curie": "MONDO:0005648", "names": ["ai", "AR", "Corrigan's disease", "aortic incompetence", "Aortic Incompetence", "Aortic incompetence", "aorta; incompetency", "Incompetence;aortic", "AORTIC INCOMPETENCE", "Aortic Regurgitation", "Aortic insufficiency", "AORTIC REGURGITATION", "Aortic regurgitation", "Regurgitation;aortic", "aorta; insufficiency", "Aortic Insufficiency", "Incompetence, Aortic", "AORTIC INSUFFICIENCY", "aortic regurgitation", "aortic insufficiency", "insufficiency; aortic", "Regurgitation, Aortic", "AI - Aortic incompetence", "AR - Aortic regurgitation", "AORTIC VALVE INCOMPETENCE", "Aortic Valve Incompetence", "Aortic regurgitation, NOS", "Aortic valve incompetence", "aortic valve incompetence", "aortic valve regurgitation", "aortic valve; incompetency", "incompetency; aortic valve", "AORTIC VALVE REGURGITATION", "Aortic Valve Insufficiency", "aortic valve insufficiency", "Incompetence, Aortic Valve", "Aortic Valve Regurgitation", "Aortic Valve regurgitation", "Aortic valve regurgitation", "Aortic valve insufficiency", "AORTIC VALVE INSUFFICIENCY", "AORTIC VALVE, INCOMPETENCE", "AORTIC VALVE, REGURGITATION", "Regurgitation, Aortic Valve", "AORTIC VALVE, INSUFFICIENCY", "aortic valve; regurgitation", "Insufficiency, Aortic Valve", "aortic valve; insufficiency", "Aortic (valve) insufficiency", "Rheumatic aortic incompetence", "Aortic valve incompetence, NOS", "rheumatic aortic regurgitation", "Rheumatic aortic regurgitation", "rheumatic aortic insufficiency", "Rheumatic aortic insufficiency", "Aortic valve insufficiency, NOS", "Aortic incompetence - rheumatic", "Aortic valve regurgitation, NOS", "insufficiency; aortic, rheumatic", "regurgitation; aortic, rheumatic", "aortic regurgitation (diagnosis)", "Rheumatic aortic valve regurgitation", "rheumatic aortic valve insufficiency", "rheumatic aortic valve regurgitation", "Rheumatic aortic valve insufficiency", "Aortic valve regurgitation (disorder)", "Rheumatic aortic regurgitation (disorder)", "Aortic Valve Insufficiency/ Regurgitation", "rheumatic aortic regurgitation (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aortic valve insufficiency", "shortest_name_length": 2}
{"curie": "MONDO:0020488", "names": ["atypical PSP syndrome", "atypical progressive supranuclear palsy syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical progressive supranuclear palsy syndrome", "shortest_name_length": 21}
{"curie": "MONDO:0007962", "names": ["MACRODACTYLY", "macrodactyly", "Macrodactyly", "Megalodactyly", "megalodactyly", "Dactylomegaly", "MEGALODACTYLY", "Finger overgrowth", "Congenital macrodactyly", "Congenital macrodactylia", "Congenital hypertrophy of digit", "Congenital macrodactyly (disorder)", "macrodactyly, somatic, (3), cerebral cavernous malformations 4, somatic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "megalodactyly", "shortest_name_length": 12}
{"curie": "MONDO:0001572", "names": ["Fibroid", "fibroid", "fibroids", "FIBROIDS", "Fibroids", "Leiomyoma", "LEIOMYOMA", "leiomyoma", "leiomyomas", "Leiomyomas", "Fibromyoma", "fibromyoma", "fibromyomas", "Fibromyomas", "Leiomyoma NOS", "fibroid tumor", "tumor fibroid", "Fibroid Tumor", "Leiomyoma, NOS", "fibroids tumor", "fibroid tumors", "Tumor, Fibroid", "Leiomyofibroma", "leiomyofibroma", "Fibroleiomyoma", "Fibroid Tumors", "Tumors, Fibroid", "fibroids tumors", "Fibroid Neoplasm", "fibroid neoplasm", "LEIOMYOMA, BENIGN", "leiomyoma, benign", "Leiomyomatous Tumor", "leiomyomatous tumor", "Plexiform leiomyoma", "Leiomyomatous Neoplasm", "leiomyomatous neoplasm", "Leiomyomatous neoplasm", "Leiomyoma (morphologic abnormality)", "leiomyomatous neoplasm (morphologic abnormality)", "Leiomyomatous neoplasm (morphologic abnormality)", "Soft tissue tumor of smooth muscle differentiation", "Soft tissue tumour of smooth muscle differentiation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leiomyoma", "shortest_name_length": 7}
{"curie": "UMLS:C4724959", "names": ["Refractory Stage 0 Bladder Cancer", "Refractory Stage 0 Bladder Cancer AJCC v6 and v7", "Refractory Bladder Carcinoma In Situ AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Stage 0 Bladder Cancer AJCC v6 and v7", "shortest_name_length": 33}
{"curie": "UMLS:C5420235", "names": ["Oral Cavity Myeloid Sarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oral Cavity Myeloid Sarcoma", "shortest_name_length": 27}
{"curie": "UMLS:C5239078", "names": ["Metastatic Soft Tissue Leiomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Soft Tissue Leiomyosarcoma", "shortest_name_length": 37}
{"curie": "MONDO:0012286", "names": ["myopathy, autophagic vacuolar, infantile-onset"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy, autophagic vacuolar, infantile-onset", "shortest_name_length": 46}
{"curie": "MONDO:0100004", "names": ["MACS", "nc MCAS", "nc-MCAS", "mast cell activation disease", "mast cell activation syndrome", "Mast cell activation syndrome", "Mast Cell Activation Syndrome", "Mast Cell Activation Syndromes", "disorder of mast cell activation", "Mast cell activation syndrome, NOS", "MCAD - mast cell activation disorder", "Nonclonal Mast Cell Activation Syndrome", "Idiopathic Mast Cell Activation Disorder", "Non Clonal Mast Cell Activation Syndrome", "Non-Clonal Mast Cell Activation Syndrome", "Non-Clonal Mast Cell Activation Disorder", "Mast cell activation syndrome (disorder)", "Non Clonal Mast Cell Activation Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mast cell activation syndrome", "shortest_name_length": 4}
{"curie": "UMLS:C0277644", "names": ["Electrocution", "electrocution", "electrocutions", "Death by electrocution", "electrocution (diagnosis)", "Death by electrocution (event)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Death by electrocution", "shortest_name_length": 13}
{"curie": "MONDO:0041903", "names": ["Arthritis gonococcal", "gonococcal arthritis", "Gonococcal arthritis", "Gonococcal Arthritis", "GONOCOCCAL ARTHRITIS", "ARTHRITIS GONOCOCCAL", "Gonococcal rheumatism", "gonococcal rheumatism", "ARTHRITIS, GONOCOCCAL", "Gonococcal joint infection", "gonococcal joint infection", "gonococcal infection of joint", "Gonococcal infection of joint", "gonococcal infection of a joint", "Gonococcal infection of joint NOS", "Gonococcal infection of joint, NOS", "Gonococcal infection of joint (disorder)", "gonococcal infection of joint (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gonococcal infection of joint", "shortest_name_length": 20}
{"curie": "MONDO:0020748", "names": ["STSL2", "SITOSTEROLEMIA 2", "sitosterolemia 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "sitosterolemia 2", "shortest_name_length": 5}
{"curie": "UMLS:C2938878", "names": ["Herbal interaction", "Herbal interactions"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Herbal interaction", "shortest_name_length": 18}
{"curie": "MONDO:0005283", "names": ["RETINOPATHY", "retinopathy", "Retinopathy", "Retina issue", "retinopathies", "Abnormal retina", "retinal disease", "Retinopathy NOS", "Retinal disease", "Disorder;retina", "Retinal Disease", "retina disorder", "disease retinal", "Retinal Disorder", "retinal disorder", "disorders retina", "retinal diseases", "Retinal Diseases", "diseases retinal", "Retinal disorder", "Disease, Retinal", "DISORDER RETINAL", "Disorder retinal", "Retinopathy, NOS", "retina; disorder", "RETINAL DISORDER", "disorders retinal", "Retinal Disorders", "Diseases, Retinal", "retina eye disease", "RETINA ABNORMALITY", "RETINAL ABNORMALITY", "Retinal disease, NOS", "Retinal disorder NOS", "Anomaly of the retina", "eye disease of retina", "Retinal disorder, NOS", "RETINAL ABNORMALITIES", "Retinal abnormalities", "retinopathy (diagnosis)", "Abnormality of the retina", "Abnormal retinal morphology", "Retinal disorder (disorder)", "retinal disorder (diagnosis)", "Unspecified retinal disorder", "disease (or disorder); retina", "Retinal disorder, unspecified", "Noninflammatory retina disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retinal disorder", "shortest_name_length": 11}
{"curie": "UMLS:C1333044", "names": ["CMML-2", "Chronic Myelomonocytic Leukemia-2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic Myelomonocytic Leukemia-2", "shortest_name_length": 6}
{"curie": "UMLS:C5206667", "names": ["Penile Leiomyosarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Penile Leiomyosarcoma", "shortest_name_length": 21}
{"curie": "MONDO:0019543", "names": ["acquired aneurysmal subarachnoid hemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acquired aneurysmal subarachnoid hemorrhage", "shortest_name_length": 43}
{"curie": "MONDO:0019956", "names": ["encephalitis", "ENCEPHALITIS", "Encephalitis", "Encephalitis NOS", "Encephalitis, NOS", "brain inflammation", "Brain inflammation", "Brain Inflammation", "Brain Inflammations", "Inflammation, Brain", "inflammation; brain", "brain; inflammation", "inflammation; cerebral", "cerebral; inflammation", "Encephalitis (disorder)", "Infectious encephalitis", "encephalitis (diagnosis)", "inflammation of the brain"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephalitis", "shortest_name_length": 12}
{"curie": "MONDO:0005357", "names": ["CJD", "cjd", "CJ disease", "Creutzfeldt-Jakob", "Jakob-Creutzfeldt", "Creutzfeld-Jakob disease", "Creutzfeld-Jacob disease", "Jacob-Creutzfeld disease", "Creutzfeldt Jacob disease", "CREUTZFELDT-JAKOB DISEASE", "Jakob-Creutzfeldt disease", "jakob-creutzfeldt disease", "Creutzfeldt-Jacob disease", "creutzfeldt-jakob disease", "Jakob Creutzfeldt Disease", "JAKOB-CREUTZFELDT DISEASE", "Creutzfeldt-Jacob Disease", "creutzfeldt jakob disease", "Creutzfeldt Jakob disease", "Jakob-Creutzfeldt Disease", "Creutzfeldt-Jakob Disease", "Creutzfeldt Jakob Disease", "Creutzfeldt-Jakob disease", "Creutzfeldt Jacob Disease", "Disease, Jakob-Creutzfeldt", "jakob-creutzfeldt syndrome", "Disease, Creutzfeldt Jacob", "Jakob-Creutzfeldt Syndrome", "creutzfeldt-jakob syndrome", "Jakob Creutzfeldt Syndrome", "Disease, Creutzfeldt-Jakob", "Creutzfeldt-Jakob Syndrome", "Creutzfeldt Jakob Syndrome", "creutzfeldt jakob syndrome", "Creutzfeldt Jacob syndrome", "Jacob Disease, Creutzfeldt", "Syndrome, Creutzfeldt-Jakob", "Creutzfeldt-Jakob's disease", "Syndrome, Jakob-Creutzfeldt", "Transmissible virus dementia", "transmissible virus dementia", "CJD (Creutzfeldt-Jakob Disease)", "JCD - Jakob-Creutzfeldt disease", "CJD (Creutzfeldt Jakob Disease)", "CJD (Creutzfeldt Jakob disease)", "CJD - Creutzfeldt-Jakob disease", "Classic Creutzfeldt-Jakob Disease", "Creutzfeldt-Jakob pseudosclerosis", "classic Creutzfeldt-Jakob disease", "SPONGIFORM ENCEPHALOPATHY SUBACUTE", "Subacute Spongiform Encephalopathy", "Subacute spongiform encephalopathy", "pseudosclerosis; spastic (etiology)", "spastic; pseudosclerosis (etiology)", "Spongiform Encephalopathy, Subacute", "Encephalopathy, Subacute Spongiform", "Jakob-Creutzfeldt disease (disorder)", "Subacute Spongiform Encephalopathies", "Spongiform Encephalopathies, Subacute", "Encephalopathies, Subacute Spongiform", "Creutzfeldt-Jakob disease (diagnosis)", "Creutzfeldt-Jakob disease, unspecified", "Jakob-Creutzfeldt disease, unspecified", "spastic; pseudosclerosis (manifestation)", "pseudosclerosis; spastic (manifestation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Creutzfeldt Jacob disease", "shortest_name_length": 3}
{"curie": "MONDO:0010314", "names": ["BPP", "CBPS", "BPPX", "PMGX", "Perisylvian syndrome", "Bilateral perisylvian polymicrogyria", "Polymicrogyria, bilateral perisylvian", "Congenital bilateral perisylvian syndrome", "PERISYLVIAN SYNDROME, CONGENITAL BILATERAL", "Perisylvian syndrome, congenital bilateral", "perisylvian syndrome, congenital bilateral", "POLYMICROGYRIA, BILATERAL PERISYLVIAN, X-LINKED", "polymicrogyria, bilateral perisylvian, X-linked", "Congenital bilateral perisylvian syndrome (disorder)", "polymicrogyria, bilateral perisylvian, X-linked dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "polymicrogyria, bilateral perisylvian, X-linked", "shortest_name_length": 3}
{"curie": "EFO:0006315", "names": ["thiopurine immunosuppressant-induced pancreatitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thiopurine immunosuppressant-induced pancreatitis", "shortest_name_length": 49}
{"curie": "UMLS:C0852919", "names": ["animal scratch", "Animal scratch", "Animal scratches", "animal scratches", "Animal scratch NOS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Animal scratch", "shortest_name_length": 14}
{"curie": "UMLS:C1335361", "names": ["Parotid Lymphangioma", "Lymphangioma of Parotid", "Parotid Gland Lymphangioma", "Lymphangioma of the Parotid", "Lymphangioma of Parotid Gland", "Lymphangioma of the Parotid Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parotid Gland Lymphangioma", "shortest_name_length": 20}
{"curie": "MONDO:0011760", "names": ["MPSIS", "MPS1S", "MPS V", "Scheie", "MPS1-S", "MPS I S", "MPS5, formerly", "MPS5, FORMERLY", "Scheie syndrome", "scheie syndrome", "MPS V, formerly", "Scheie Syndrome", "MPS V, FORMERLY", "SCHEIE SYNDROME", "scheies syndrome", "Scheie's Syndrome", "Scheie's syndrome", "scheie's syndrome", "Syndrome, Scheie's", "Mucopolysaccharidosis 5", "Mucopolysaccharidosis V", "Mucopolysaccharidosis IS", "mucopolysaccharidosis Is", "Mucopolysaccharidosis I S", "Mucopolysaccharidosis I-S", "Scheie disease MPS type 1S", "mucopolysaccharidosis type V", "Mucopolysaccharidosis type IS", "Mucopolysaccharidosis type 1S", "MUCOPOLYSACCHARIDOSIS TYPE IS", "mucopolysaccharidosis type IS", "mucopolysaccharidosis type 1S", "Mucopolysaccharidosis Type Is", "Mucopolysaccharidosis, MPS-I-S", "type I-S mucopolysaccharidosis", "Mucopolysaccharidosis type I-S", "L-iduronidase deficiency, Scheie type", "Mucopolysaccharidosis, type V (MPS V)", "Mucopolysaccharidosis type I mild form", "MUCOPOLYSACCHARIDOSIS TYPE V, FORMERLY", "mucopolysaccharidosis type V, formerly", "mucopolysaccharidosis type V (diagnosis)", "MPS 1-S - Mucopolysaccharidosis type I-S", "Mucopolysaccharidosis type I-S (disorder)", "type I-S mucopolysaccharidosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Scheie syndrome", "shortest_name_length": 5}
{"curie": "UMLS:C1512976", "names": ["Malignant Vulvar Sweat Gland Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Vulvar Sweat Gland Neoplasm", "shortest_name_length": 37}
{"curie": "MONDO:0044753", "names": ["lumbar stenosis", "LUMBAR SPINE STENOSIS", "lumbar spine stenosis", "Spinal stenosis lumbar", "lumbar spinal stenosis", "spinal lumbar stenosis", "LUMBAR SPINAL STENOSIS", "Lumbar spinal stenosis", "Lumbar Spinal Stenosis", "spinal stenosis lumbar", "Narrow lumbar spinal canal", "lumbar stenosis (diagnosis)", "Lumbar spinal canal stenosis", "lumbar region spinal stenosis", "Spinal stenosis; lumbar region", "Spinal stenosis, lumbar region", "spinal stenosis of lumbar region", "Spinal stenosis of lumbar region", "Spinal stenosis, lumbar region NOS", "Spinal stenosis of lumbar region NOS", "Spinal stenosis of lumbar region (disorder)", "lumbar region of vertebral column spinal stenosis", "spinal stenosis of lumbar region of vertebral column"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lumbar spinal stenosis", "shortest_name_length": 15}
{"curie": "MONDO:0011542", "names": ["PSORS6", "psoriasis 6", "psoriasis susceptibility 6", "PSORIASIS 6, SUSCEPTIBILITY TO", "psoriasis 6, susceptibility to", "PSORIASIS SUSCEPTIBILITY 6 (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "psoriasis 6, susceptibility to", "shortest_name_length": 6}
{"curie": "UMLS:C0264939", "names": ["polyangitis", "Polyangiitis", "polyangiitis", "Systemic Vasculitis", "systemic vasculitis", "VASCULITIS SYSTEMIC", "Systemic vasculitis", "Vasculitis, Systemic", "Systemic Vasculitides", "Vasculitides, Systemic", "Systemic vasculitis syndrome", "Systemic vasculitis (disorder)", "systemic vasculitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Systemic Vasculitis", "shortest_name_length": 11}
{"curie": "MONDO:0006816", "names": ["ARTHROSIS", "Arthrosis", "arthrosis", "Arthropathy", "arthropathy", "ARTHROPATHY", "arthropathic", "Joint Disease", "arthropathies", "Joint disease", "Arthropathies", "joint disease", "Arthrosis NOS", "Disorder joint", "joint diseases", "joint disorder", "Joint disorder", "Arthrosis, NOS", "Joint Diseases", "Joint Disorder", "DISORDER JOINT", "JOINT DISORDER", "joint; disorder", "Arthropathy NOS", "Joint Infection", "joint disorders", "Joint disorders", "joint infection", "disorder, Joint", "Joint infection", "infection joint", "arthropathy nos", "Joint Disorders", "ARTHROPATHY, NOS", "Arthropathy, NOS", "Joints--Diseases", "infections joint", "infection joints", "Disease of joint", "Dysfunction;joint", "Joint dysfunction", "disorder of joint", "JOINT DYSFUNCTION", "articular disease", "Disorder of joint", "Articular disease", "joint dysfunction", "ARTHROPATHY (NOS)", "infections joints", "Arthropathy (NOS)", "diseases of joints", "Diseases of Joints", "Joint disease, NOS", "Joint disorder NOS", "osteoarthrosis; joint", "Disease of the joints", "Disorder of joint, NOS", "skeletal joint disease", "diseases of the joints", "DISEASES OF THE JOINTS", "infectious arthropathy", "Arthrosis, unspecified", "Infectious arthropathy", "Arthropathy (disorder)", "ankylosis of hand joint", "arthropathy (diagnosis)", "Unspecified arthropathy", "Infectious arthropathies", "Arthropathy, unspecified", "infectious joint disease", "disease of skeletal joint", "Unspecified joint disorder", "ankylosis of forearm joint", "joint disorder (diagnosis)", "disorder of skeletal joint", "ankylosis of joint of hand", "Ankylosis of joint of hand", "Infectious arthropathy, NOS", "Joint disorder, unspecified", "joint infection (diagnosis)", "Joint ankylosis of the hand", "ankylosis of lower leg joint", "Infectious disorder of joint", "ankylosis of upper arm joint", "Ankylosis of multiple joints", "ankylosis of multiple joints", "disease (or disorder); joint", "ankylosis of joint of forearm", "Ankylosis of joint of forearm", "Unspecified disorder of joint", "Joint ankylosis of the forearm", "ankylosis of joint of lower leg", "Ankylosis of joint of upper arm", "Ankylosis of joint of lower leg", "ankylosis of joint of upper arm", "Joint ankylosis of the upper arm", "Arthropathy related to infection", "Joint ankylosis of the lower leg", "ankylosis of ankle and foot joint", "Infectious arthropathies (M00-M02)", "skeletal joint disease or disorder", "Infection-associated arthritis, NOS", "ankylosis of joint of multiple sites", "Arthropathy associated with infection", "Joint ankylosis of the ankle and foot", "disease or disorder of skeletal joint", "ankylosis of joint of shoulder region", "Arthropathy associated with infections", "Unspecified joint disorder, other site", "Joint ankylosis of the shoulder region", "arthropathy associated with infections", "Ankylosis of joint of ankle and/or foot", "ankylosis of joint of ankle and/or foot", "Infectious disorder of joint (disorder)", "Joint ankylosis of the ankle and/or foot", "Arthropathy, unspecified, site unspecified", "Arthropathy associated with infection, NOS", "Unspecified joint disorder, site unspecified", "ankylosis of joint of pelvic region and thigh", "Joint ankylosis of the pelvic region and thigh", "Unspecified disorder of joint, site unspecified", "Arthropathy associated with infection (disorder)", "arthropathy associated with infections (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "arthropathy", "shortest_name_length": 9}
{"curie": "MONDO:0006400", "names": ["salivary gland acinic cell tumor", "Salivary Gland Acinic Cell Tumor", "salivary gland acinic cell cancer", "acinic cell tumor, salivary gland", "Salivary Gland Acinic Cell Cancer", "Salivary Gland Acinic Cell Neoplasm", "Acinic Cell Tumor of Salivary Gland", "salivary gland acinic cell neoplasm", "acinic cell tumor of salivary gland", "Salivary Gland Acinic Cell Carcinoma", "salivary gland acinic cell carcinoma", "Acinic Cell Neoplasm of Salivary Gland", "acinic cell neoplasm of salivary gland", "Acinic cell carcinoma of salivary gland", "acinic cell carcinoma of salivary gland", "Acinic Cell Tumor of the Salivary Gland", "acinic cell tumor of the salivary gland", "Acinic Cell Carcinoma of Salivary Gland", "Acinic Cell Neoplasm of the Salivary Gland", "acinic cell neoplasm of the salivary gland", "acinic cell carcinoma of the salivary gland", "Acinic Cell Carcinoma of the Salivary Gland"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "salivary gland acinic cell carcinoma", "shortest_name_length": 32}
{"curie": "MONDO:0021144", "names": ["ovarian clear cell tumor", "Ovarian Clear Cell Tumor", "Clear cell tumor of ovary", "clear cell ovarian cancer", "Clear cell tumour of ovary", "Ovarian Clear Cell Neoplasm", "ovarian neoplasm clear cell", "ovarian clear cell neoplasm", "Mesonephroid tumor of ovary", "Mesonephroid tumour of ovary", "clear cell neoplasm of ovary", "clear cell neoplasm of ovary (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian clear cell tumor", "shortest_name_length": 24}
{"curie": "UMLS:C0342779", "names": ["Complex V deficiency", "ATP synthase deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ATP synthase deficiency", "shortest_name_length": 20}
{"curie": "UMLS:C4050413", "names": ["DDIT4L", "DDIT4L ALL", "DDIT4L Acute Lymphoblastic Leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DDIT4L Acute Lymphoblastic Leukemia", "shortest_name_length": 6}
{"curie": "MONDO:0017157", "names": ["PH due to lung disease and/or hypoxia", "PH owing to lung disease and/or hypoxia", "Pulmonary hypertension due to lung disease and/or hypoxia", "pulmonary hypertension due to lung disease and/or hypoxia", "Pulmonary hypertension owing to lung disease and/or hypoxia", "pulmonary hypertension owing to lung disease and/or hypoxia", "Pulmonary hypertension due to lung disease and/or hypoxia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pulmonary hypertension owing to lung disease and/or hypoxia", "shortest_name_length": 37}
{"curie": "MONDO:0014381", "names": ["PFIC4", "TJP2 deficit", "Progressive familial intrahepatic cholestasis 4", "progressive familial intrahepatic cholestasis 4", "cholestasis, progressive familial intrahepatic 4", "Cholestasis, progressive familial intrahepatic 4", "CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 4", "cholestasis, progressive familial intrahepatic, 4", "TJP2 progressive familial intrahepatic cholestasis", "Progressive familial intrahepatic cholestasis type 4", "progressive familial intrahepatic cholestasis type 4", "cholestasis, progressive familial intrahepatic, type 4", "PFIC4 Progressive familial intrahepatic cholestasis type 4", "progressive familial intrahepatic cholestasis caused by mutation in TJP2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cholestasis, progressive familial intrahepatic, 4", "shortest_name_length": 5}
{"curie": "MONDO:0001130", "names": ["Nasal Cavity Lymphoma", "nasal cavity lymphoma", "lymphoma of nasal cavity", "Lymphoma of Nasal Cavity", "Lymphoma of the Nasal Cavity", "Lymphoma of the nasal cavity", "lymphoma of the nasal cavity", "primary nasal cavity lymphoma", "Primary Nasal Cavity Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nasal cavity lymphoma", "shortest_name_length": 21}
{"curie": "MONDO:0000468", "names": ["chb", "Heart Block", "Complete AV Block", "complete av block", "complete AV block", "av block complete", "Complete AV block", "AV block complete", "AV BLOCK COMPLETE", "Third degree block", "AV block-3rd degree", "complete heart block", "HEART BLOCK COMPLETE", "Complete Heart Block", "Block;heart 3 degree", "heart block complete", "block complete heart", "Block;heart;complete", "Complete heart block", "Heart block complete", "third degree AV block", "Third Degree AV Block", "AV block third degree", "Third degree AV block", "AV Block Third Degree", "HEART BLOCK, COMPLETE", "AV BLOCK THIRD DEGREE", "3rd degree heart block", "third degree A-V block", "Heart block AV complete", "HEART BLOCK AV COMPLETE", "heart block third degree", "third degree heart block", "Complete heart block NOS", "THIRD DEGREE HEART BLOCK", "Heart block third degree", "Third-degree heart block", "Third degree heart block", "CHB - Complete heart block", "Heart block AV third degree", "HEART BLOCK AV THIRD DEGREE", "Complete Atrioventricular Block", "Complete atrioventricular block", "atrioventricular block complete", "Atrioventricular block complete", "complete atrioventricular block", "Atrioventricular block, complete", "atrioventricular; block, complete", "High grade atrioventricular block", "block; atrioventricular, complete", "third-degree atrioventricular block", "third degree atrioventricular block", "Third degree atrioventricular block", "THIRD DEGREE ATRIOVENTRICULAR BLOCK", "Third Degree Atrioventricular Block", "Atrioventricular block third degree", "Atrioventricular Block, Third Degree", "atrioventricular block, third degree", "block; atrioventricular, third degree", "atrioventricular; block, third degree", "heart; block, complete (atrioventricular)", "block; heart, complete (atrioventricular)", "Third degree atrioventricular heart block", "Complete atrioventricular block (disorder)", "block; heart, third degree (atrioventricular)", "heart; block, third degree (atrioventricular)", "non-congenital complete atrioventricular block", "Non-Congenital Complete Atrioventricular Block", "third degree atrioventricular block (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "third-degree atrioventricular block", "shortest_name_length": 3}
{"curie": "MONDO:0005118", "names": ["HGE", "Anaplasmosis (diagnosis)", "human granulocytic ehrlichiosis", "human granulocytic anaplasmosis", "Human granulocytic ehrlichiosis", "infection by Anaplasma phagocytophilum", "Infection by Anaplasma phagocytophilum", "human ehrlichial infection, human granulocytic type", "human anaplasmosis due to Anaplasma phagocytophilum", "Human anaplasmosis due to Anaplasma phagocytophilum", "human anaplasmosis caused by Anaplasma phagocytophilum", "Human anaplasmosis caused by Anaplasma phagocytophilum", "Human anaplasmosis caused by Anaplasma phagocytophilum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "human granulocytic ehrlichiosis", "shortest_name_length": 3}
{"curie": "MONDO:0003894", "names": ["mediastinal melanotic schwannoma", "Mediastinal Melanotic Schwannoma", "Mediastinal Melanocytic Schwannoma", "mediastinal melanocytic schwannoma", "mediastinal melanocytic neurilemmoma", "Mediastinal Melanocytic Neurilemmoma", "Melanocytic Schwannoma of Mediastinum", "melanocytic Schwannoma of mediastinum", "melanocytic schwannoma of mediastinum", "Melanocytic Neurilemmoma of Mediastinum", "melanocytic neurilemmoma of mediastinum", "Melanocytic Schwannoma of the Mediastinum", "melanocytic schwannoma of the mediastinum", "melanocytic neurilemmoma of the mediastinum", "Melanocytic Neurilemmoma of the Mediastinum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mediastinal melanocytic neurilemmoma", "shortest_name_length": 32}
{"curie": "MONDO:0021498", "names": ["Benign Placenta Tumor", "benign placenta tumor", "benign placental tumor", "Benign Placental Tumor", "Tuberculosis, Cutaneous", "benign placenta neoplasm", "benign tumor of placenta", "placenta benign neoplasm", "Benign Tumor of Placenta", "Benign Placenta Neoplasm", "Neoplasm benign;placenta", "Benign Placental Neoplasm", "benign placental neoplasm", "benign neoplasm of placenta", "Placental Neoplasms, Benign", "placental neoplasms, benign", "Benign neoplasm of placenta", "Benign Neoplasm of Placenta", "Benign Tumor of the Placenta", "benign tumor of the placenta", "benign neoplasm of the placenta", "Benign Neoplasm of the Placenta", "placental disorders benign neoplasm", "Benign neoplasm of placenta (disorder)", "benign neoplasm of placenta (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "benign neoplasm of placenta", "shortest_name_length": 21}
{"curie": "UMLS:C1334555", "names": ["Male Reproductive System Precancerous Condition"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Male Reproductive System Precancerous Condition", "shortest_name_length": 47}
{"curie": "UMLS:C1336447", "names": ["Stage I AIDS-Related Anal Canal Cancer", "Stage I AIDS-Related Anal Canal Cancer AJCC v7", "Stage I AIDS-Related Anal Canal Cancer AJCC v6", "Stage I AIDS-Related Anal Carcinoma AJCC v6 and v7", "Stage I AIDS-Related Anal Canal Cancer AJCC v6 and v7", "Stage I AIDS-Related Anal Canal Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I AIDS-Related Anal Canal Cancer AJCC v6 and v7", "shortest_name_length": 38}
{"curie": "UMLS:C1334650", "names": ["Mediastinal Chondroma", "Chondroma of Mediastinum", "Chondroma of the Mediastinum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Mediastinal Chondroma", "shortest_name_length": 21}
{"curie": "MONDO:0018623", "names": ["Psychosis;puerperal", "puerperal psychosis", "Postnatal psychosis", "Puerperal Psychosis", "Puerperal psychosis", "postnatal psychosis", "psychosis puerperal", "PSYCHOSIS POSTPARTUM", "Postpartum psychosis", "psychosis; puerperal", "postpartum psychosis", "puerperal; psychosis", "Postpartum Psychosis", "Psychosis;postpartum", "POSTPARTUM PSYCHOSIS", "Psychosis postpartum", "psychosis; postpartum", "postpartum; psychosis", "Puerperal psychosis, NOS", "puerperal psychosis (diagnosis)", "Postpartum psychosis (disorder)", "disorder; mental, puerperal, psychotic", "mental; disorder, puerperal, psychotic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postpartum psychosis", "shortest_name_length": 19}
{"curie": "UMLS:C0221152", "names": ["OBSTIPATION", "obstipation", "Obstipation", "Obstipation (disorder)", "intractable constipation", "Intractable constipation", "total stoppage of bowel movement", "total stoppage of bowel movement (symptom)", "total stoppage of bowel movement (obstipation)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Obstipation", "shortest_name_length": 11}
{"curie": "UMLS:C5206628", "names": ["Invasive Adenocarcinoma in Adenomatous Polyp"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Invasive Adenocarcinoma in Adenomatous Polyp", "shortest_name_length": 44}
{"curie": "MONDO:0008109", "names": ["OCP", "Ocular cicatricial pemphigoid", "OCULAR CICATRICIAL PEMPHIGOID", "Ocular Cicatricial Pemphigoid", "ocular cicatricial pemphigoid", "Cicatricial ocular pemphigoid", "pemphigoid, ocular cicatricial", "Pemphigoid, Ocular Cicatricial", "cicatricial pemphigoid, ocular", "Cicatricial Pemphigoid, Ocular", "Ocular Cicatricial Pemphigoids", "Cicatricial Pemphigoids, Ocular", "Pemphigoids, Ocular Cicatricial", "OCP - Ocular cicatricial pemphigoid", "Ocular cicatricial pemphigoid (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ocular cicatricial pemphigoid", "shortest_name_length": 3}
{"curie": "UMLS:C4054373", "names": ["Nephrotic Syndrome - NPHS2 Associated"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nephrotic Syndrome - NPHS2 Associated", "shortest_name_length": 37}
{"curie": "UMLS:C5557311", "names": ["DS Stage IB Plasma Cell Myeloma", "Durie/Salmon Stage IB Plasma Cell Myeloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "DS Stage IB Plasma Cell Myeloma", "shortest_name_length": 31}
{"curie": "UMLS:C4721647", "names": ["Stage III Esophagus Adenocarcinoma", "Stage III Esophageal Adenocarcinoma", "Oesophageal Adenocarcinoma Stage III", "Esophageal Adenocarcinoma, Stage III", "Stage III Adenocarcinoma of Esophagus", "Stage III Adenocarcinoma of the Esophagus", "Stage III Esophageal Adenocarcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Esophageal Adenocarcinoma AJCC v7", "shortest_name_length": 34}
{"curie": "UMLS:C0752098", "names": ["Autosomal Dominant Parkinsonism", "Parkinsonism, Autosomal Dominant", "Dominant Parkinsonism, Autosomal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Autosomal Dominant Parkinsonism", "shortest_name_length": 31}
{"curie": "UMLS:C0521753", "names": ["Temporary nystagmus", "nystagmus temporary", "Temporary Nystagmus", "Nystagmus, Temporary", "Temporary nystagmus (disorder)", "Temporary nystagmus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Temporary Nystagmus", "shortest_name_length": 19}
{"curie": "UMLS:C5239072", "names": ["Unresectable Myxoid Liposarcoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Myxoid Liposarcoma", "shortest_name_length": 31}
{"curie": "MONDO:0006377", "names": ["Pleural Biphasic Mesothelioma", "pleural biphasic mesothelioma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pleural biphasic mesothelioma", "shortest_name_length": 29}
{"curie": "MONDO:0032891", "names": ["ANIB12", "intracranial berry aneurysm 12", "aneurysm, intracranial berry, 12", "ANEURYSM, INTRACRANIAL BERRY, 12"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "aneurysm, intracranial berry, 12", "shortest_name_length": 6}
{"curie": "MONDO:0014292", "names": ["CC2L", "LKPAT", "Leucoencephalopathy with ataxia", "LEUKOENCEPHALOPATHY WITH ATAXIA", "leukoencephalopathy with ataxia", "Leukoencephalopathy with ataxia", "Leukoencephalopathy with Ataxia", "CLCN2-Related Leukoencephalopathy", "CLCN2-related leucoencephalopathy", "CLCN2-related leukoencephalopathy", "CLCN2 (chloride voltage-gated channel 2) related leucoencephalopathy", "CLCN2 (chloride voltage-gated channel 2) related leukoencephalopathy", "Leukoencephalopathy with mild cerebellar ataxia and white matter edema", "leukoencephalopathy with mild cerebellar ataxia and white matter edema", "Leucoencephalopathy with mild cerebellar ataxia and white matter oedema", "Leukoencephalopathy with mild cerebellar ataxia and white matter edema (disorder)", "leukoencephalopathy with mild cerebellar ataxia and white matter edema (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leukoencephalopathy with mild cerebellar ataxia and white matter edema", "shortest_name_length": 4}
{"curie": "UMLS:C4521783", "names": ["Stage I Gastric (Stomach) Cancer", "Pathologic Stage I Gastric Cancer AJCC v8", "Pathologic Stage I Gastric Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pathologic Stage I Gastric Cancer AJCC v8", "shortest_name_length": 32}
{"curie": "UMLS:C1332837", "names": ["Cancer with Regional Lymph Node Involvement", "Malignant Neoplasm with Regional Lymph Node Involvement"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Malignant Neoplasm with Regional Lymph Node Involvement", "shortest_name_length": 43}
{"curie": "MONDO:0030484", "names": ["IMD89", "IMMUNODEFICIENCY 89 AND AUTOIMMUNITY", "immunodeficiency 89 and autoimmunity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "immunodeficiency 89 and autoimmunity", "shortest_name_length": 5}
{"curie": "UMLS:C5555092", "names": ["Central Nervous System Tumor, SMARCB1-Mutant", "Central Nervous System SMARCB1/INI1-Deficient Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Central Nervous System SMARCB1/INI1-Deficient Tumor", "shortest_name_length": 44}
{"curie": "MONDO:0012505", "names": ["PPNAD2", "CUSHING SYNDROME, ADRENAL, DUE TO PPNAD2", "Cushing syndrome, adrenal, due to PPNAD2", "Cushing Syndrome, Adrenal, Due To PPNAD2", "PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2", "pigmented nodular adrenocortical disease, primary, 2", "Pigmented Nodular Adrenocortical Disease, Primary, 2", "PDE11A primary pigmented nodular adrenocortical disease", "PIGMENTED MICRONODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2", "pigmented micronodular adrenocortical disease, primary, 2", "Pigmented Micronodular Adrenocortical Disease, Primary, 2", "pigmented nodular adrenocortical disease, primary, type 2", "primary pigmented nodular adrenocortical disease caused by mutation in PDE11A"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pigmented nodular adrenocortical disease, primary, 2", "shortest_name_length": 6}
{"curie": "MONDO:0044991", "names": ["upper digestive tract disorder", "disease of upper digestive tract", "disorder of upper digestive tract", "upper gastrointestinal tract disease", "disorder of upper gastrointestinal tract", "Disorder of upper gastrointestinal tract", "upper digestive tract disease or disorder", "disease or disorder of upper digestive tract", "Disorder of upper gastrointestinal tract (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "upper digestive tract disorder", "shortest_name_length": 30}
{"curie": "UMLS:C5236044", "names": ["Prostate Adenocarcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Prostate Adenocarcinoma by AJCC v7 Stage", "shortest_name_length": 40}
{"curie": "MONDO:0700013", "names": ["chromosome 6 disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chromosome 6 disorder", "shortest_name_length": 21}
{"curie": "MONDO:0005718", "names": ["Coronaviridae Infection", "Infection, Coronaviridae", "Coronaviridae Infections", "Infections, Coronaviridae", "Disease due to Coronaviridae", "DISEASES DUE TO CORONAVIRIDAE", "Disease caused by Coronaviridae", "Coronaviridae infectious disease", "Disease due to coronaviridae, NOS", "Disease caused by Coronaviridae (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Coronaviridae infectious disease", "shortest_name_length": 23}
{"curie": "MONDO:0018159", "names": ["Ig-mediated MPGN", "nephrotic syndrome type 7", "aHUS with DGKE deficiency", "D-HUS with DGKE deficiency", "Immunoglobulin-mediated MPGN", "atypical HUS with DGKE deficiency", "Ig-mediated membranoproliferative glomerulonephritis", "atypical hemolytic-uremic syndrome with DGKE deficiency", "hemolytic-uremic syndrome without diarrhea with DGKE deficiency", "immunoglobulin-mediated membranoproliferative glomerulonephritis", "nephrotic syndrome type 7 with membranoptoliferative glomerulonephritis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "atypical hemolytic-uremic syndrome with DGKE deficiency", "shortest_name_length": 16}
{"curie": "MONDO:0014087", "names": ["Smc2", "SMC2", "SMITH-MCCORT DYSPLASIA 2", "Smith-McCort dysplasia 2", "SMITH-McCort dysplasia 2", "RAB33B Smith-McCort dysplasia", "Smith-McCort dysplasia type 2", "Smith-McCort dysplasia caused by mutation in RAB33B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Smith-McCort dysplasia 2", "shortest_name_length": 4}
{"curie": "MONDO:0014617", "names": ["MRD38", "PRELDS", "autosomal dominant mental retardation 38", "mental retardation, autosomal dominant 38", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 38", "autosomal dominant intellectual disability 38", "mental retardation, autosomal dominant type 38", "intellectual disability, autosomal dominant 38", "intellectual disability, autosomal dominant type 38", "autosomal dominant intellectual developmental disorder 38", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 38", "autosomal dominant non-syndromic intellectual disability 38", "EEF1A2 autosomal dominant non-syndromic intellectual disability", "PSYCHOMOTOR RETARDATION, EPILEPSY, AND LANGUAGE DISABILITY SYNDROME", "psychomotor retardation, epilepsy, and language disability syndrome", "autosomal dominant non-syndromic intellectual disability caused by mutation in EEF1A2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 38", "shortest_name_length": 5}
{"curie": "MONDO:0008175", "names": ["Pacman syndrome", "PACMAN DYSPLASIA", "pacman dysplasia", "Pacman dysplasia", "Pacman dysplasia (disorder)", "Pacman dysplasia (diagnosis)", "Epiphyseal stippling with osteoclastic hyperplasia", "epiphyseal stippling with osteoclastic hyperplasia", "EPIPHYSEAL STIPPLING WITH OSTEOCLASTIC HYPERPLASIA", "Epiphyseal stippling-osteoclastic hyperplasia syndrome", "Epiphyseal stippling with osteoclastic hyperplasia syndrome", "epiphyseal stippling syndrome-osteoclastic hyperplasia syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pacman dysplasia", "shortest_name_length": 15}
{"curie": "MONDO:0016188", "names": ["qualitative or quantitative defects of alphaB-cristallin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "qualitative or quantitative defects of alphaB-cristallin", "shortest_name_length": 56}
{"curie": "MONDO:0017609", "names": ["RTD", "renotubular dysgenesis", "Renotubular dysgenesis", "Renal tubular dysgenesis", "RENAL TUBULAR DYSGENESIS", "renal tubular dysgenesis", "CROHN DISEASE, ASSOCIATION WITH", "PREECLAMPSIA, SUSCEPTIBILITY TO", "primitive renal tubule syndrome", "Primitive renal tubule syndrome", "PRIMITIVE RENAL TUBULE SYNDROME", "Allanson Pantzar McLeod syndrome", "ISCHEMIC STROKE, SUSCEPTIBILITY TO", "STROKE, ISCHEMIC, SUSCEPTIBILITY TO", "Renal tubular dysgenesis (disorder)", "renal tubular dysgenesis (diagnosis)", "essential hypertension susceptibility", "ISCHEMIC HEART DISEASE, SUSCEPTIBILITY TO", "CORONARY ARTERY SPASM 1, SUSCEPTIBILITY TO", "HYPERTENSION, ESSENTIAL, SUSCEPTIBILITY TO", "Hypertension Resistant to Conventional Therapy", "HYPERTENSION RESISTANT TO CONVENTIONAL THERAPY", "HYPERTENSION, RESISTANT TO CONVENTIONAL THERAPY", "ANGIOTENSIN I-CONVERTING ENZYME, PLASMA LEVEL OF", "ALZHEIMER DISEASE, LATE-ONSET, SUSCEPTIBILITY TO", "SEVERE ACUTE RESPIRATORY SYNDROME, PROGRESSION OF", "essential hypertension susceptibility (diagnosis)", "HYPERTENSION, PREGNANCY-INDUCED, SUSCEPTIBILITY TO", "ANGIOTENSIN I-CONVERTING ENZYME, BENIGN SERUM INCREASE", "ANGIOTENSIN I-CONVERTING ENZYME INSERTION/DELETION POLYMORPHISM", "IgA NEPHROPATHY, PROGRESSION TO RENAL FAILURE IN, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "renal tubular dysgenesis", "shortest_name_length": 3}
{"curie": "MONDO:0017234", "names": ["familial prion disease", "inherited prion disease", "hereditary prion disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited prion disease", "shortest_name_length": 22}
{"curie": "MONDO:0014714", "names": ["SCBMS", "seizures, cortical blindness, microcephaly syndrome", "SEIZURES, CORTICAL BLINDNESS, AND MICROCEPHALY SYNDROME", "seizures, cortical blindness, and microcephaly syndrome", "progressive microcephaly-seizures-cortical blindness-developmental delay syndrome", "Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome", "Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome", "Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "progressive microcephaly-seizures-cortical blindness-developmental delay syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0000893", "names": ["indeterminate bronchioloalveolar carcinoma", "Indeterminate Bronchioloalveolar Carcinoma", "Bronchiolo-alveolar carcinoma, indeterminate type", "mixed mucinous and non-mucinous bronchioloalveolar carcinoma", "Mixed Mucinous and Non-Mucinous Bronchioloalveolar Carcinoma", "Bronchiolo-alveolar carcinoma, Clara cell and goblet cell type", "mixed mucinous and non-mucinous bronchoalveolar lung carcinoma", "Bronchiolo-alveolar carcinoma, mixed mucinous and non-mucinous", "Mixed Mucinous and Non-Mucinous Bronchoalveolar Lung Carcinoma", "mixed mucinous and nonmucinous bronchioloalveolar adenocarcinoma", "Mixed Mucinous and Non-Mucinous Bronchioloalveolar Lung Carcinoma", "mixed mucinous and non-mucinous bronchioloalveolar adenocarcinoma", "mixed mucinous and non-mucinous bronchioloalveolar lung carcinoma", "Bronchiolo-alveolar carcinoma, type II pneumocyte and goblet cell type", "Minimally Invasive Lung Mixed Non-Mucinous and Mucinous Adenocarcinoma", "Bronchiolo-alveolar carcinoma, mixed mucinous and non-mucinous (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mixed mucinous and nonmucinous bronchioloalveolar adenocarcinoma", "shortest_name_length": 42}
{"curie": "UMLS:C5669879", "names": ["Diffuse Midline Glioma with EZHIP Overexpression"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diffuse Midline Glioma with EZHIP Overexpression", "shortest_name_length": 48}
{"curie": "MONDO:0018084", "names": ["Uhl", "Uhl disease", "Uhl anomaly", "UHL ANOMALY", "anomaly; Uhl", "Uhl; anomaly", "Uhl's disease", "Uhl's anomaly", "uhl's anomaly", "Uhl's disease (disorder)", "Parchment right ventricle", "parchment right ventricle", "Paper thin right ventricle", "Right ventricular hypoplasia", "right ventricular hypoplasia", "Hypoplasia of right ventricle", "Uhl's anomaly (RV hypoplasia)", "right ventricular hypoplasia (diagnosis)", "Uhl's anomaly (right ventricular hypoplasia)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uhl anomaly", "shortest_name_length": 3}
{"curie": "MONDO:0020687", "names": ["supratentorial ependymal tumor", "Supratentorial Ependymal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "supratentorial ependymal tumor", "shortest_name_length": 30}
{"curie": "OMIM:111250", "names": [], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"]}
{"curie": "UMLS:C1266147", "names": ["Typical carcinoid", "Neuroendocrine tumor grade 1", "Neuroendocrine tumour grade 1", "Grade 1 neuroendocrine carcinoma", "Grade I Neuroendocrine Carcinoma", "Neuroendocrine carcinoma, grade 1", "Well-differentiated neuroendocrine carcinoma", "Neuroendocrine tumor grade 1 (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Neuroendocrine tumor grade 1", "shortest_name_length": 17}
{"curie": "MONDO:0017836", "names": ["Degos genodermatosis", "erythrokeratoderma en cocardes", "erythrokeratoderma \"en cocardes\"", "erythrokeratoderma 'en cocardes'", "Degos genodermatosis 'en cocardes'", "erythrokeratoderma ''en cocardes''", "Degos genodermatosis \"en cocardes\"", "Degos 'en cocarde' erythrokeratoderma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "erythrokeratoderma en cocardes", "shortest_name_length": 20}
{"curie": "MONDO:0000491", "names": ["limb ischemia", "ischemia limb", "Limb ischemia", "ischemia limbs", "limb ischaemia", "Limb ischaemia", "limb ischemic disease", "ischemic disease of limb", "Limb ischemia (disorder)", "limb ischemia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "limb ischemia", "shortest_name_length": 13}
{"curie": "MONDO:0013113", "names": ["MANDP2", "metaphyseal anadysplasia 2", "METAPHYSEAL ANADYSPLASIA 2", "Metaphyseal Anadysplasia 2", "MMP9 metaphyseal anadysplasia", "metaphyseal anadysplasia type 2", "metaphyseal anadysplasia caused by mutation in MMP9"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metaphyseal anadysplasia 2", "shortest_name_length": 6}
{"curie": "MONDO:0001905", "names": ["biceps; tenosynovitis", "tenosynovitis; biceps", "Bicipital tenosynovitis", "bicipital tenosynovitis", "Bicipital tenosynovitis (disorder)", "bicipital tenosynovitis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bicipital tenosynovitis", "shortest_name_length": 21}
{"curie": "UMLS:C5418776", "names": ["Recurrent Fallopian Tube Clear Cell Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Fallopian Tube Clear Cell Adenocarcinoma", "shortest_name_length": 50}
{"curie": "UMLS:C4288779", "names": ["Major Congenital Anomaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Major Congenital Anomaly", "shortest_name_length": 24}
{"curie": "MONDO:0014939", "names": ["CMS20", "congenital myasthenic syndrome 20", "SLC5A7 congenital myasthenic syndrome", "congenital myasthenic syndrome type 20", "congenital myasthenic syndrome 20 presynaptic", "myasthenic syndrome, congenital, 20, presynaptic", "MYASTHENIC SYNDROME, CONGENITAL, 20, PRESYNAPTIC", "congenital myasthenic syndrome caused by mutation in SLC5A7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital myasthenic syndrome 20", "shortest_name_length": 5}
{"curie": "UMLS:C2699198", "names": ["17q21 Microdeletion Syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "17q21 Microdeletion Syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0021553", "names": ["Transverse myelitis", "MYELITIS TRANSVERSE", "Transverse Myelitis", "Myelitis transverse", "transverse myelitis", "myelitis transverse", "Myelitis, Transverse", "transverse; myelitis", "myelitis; transverse", "Transverse myelitis NOS", "Transverse myelopathy syndrome", "Transverse Myelopathy Syndrome", "transverse myelopathy syndrome", "transverse myelitis (diagnosis)", "Transverse Myelopathy Syndromes", "TRANSVERSE MYELITIS ACUTE OR SUBACUTE", "Transverse myelopathy syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "transverse myelitis", "shortest_name_length": 19}
{"curie": "UMLS:C5419186", "names": ["Advanced Cutaneous Squamous Cell Carcinoma of the Head and Neck"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Cutaneous Squamous Cell Carcinoma of the Head and Neck", "shortest_name_length": 63}
{"curie": "UMLS:C3665900", "names": ["Intraspinal bleeding", "Intraspinal hemorrhage", "Intraspinal haemorrhage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intraspinal bleeding", "shortest_name_length": 20}
{"curie": "MONDO:0100060", "names": ["Congenital/Infantile Spindle Cell Rhabdomyosarcoma with VGLL2/NCOA2/CITED2 Rearrangements", "congenital/infantile spindle cell rhabdomyosarcoma with VGLL2/NCOA2/CITED2 rearrangements"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital/infantile spindle cell rhabdomyosarcoma with VGLL2/NCOA2/CITED2 rearrangements", "shortest_name_length": 89}
{"curie": "UMLS:C1708769", "names": ["Lung Clear Cell Adenocarcinoma", "Clear cell adenocarcinoma of lung", "clear cell adenocarcinoma of lung", "Clear cell adenocarcinoma of lung (disorder)", "clear cell adenocarcinoma of lung (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clear cell adenocarcinoma of lung", "shortest_name_length": 30}
{"curie": "UMLS:C0542142", "names": ["Recurrent laryngeal nerve palsy", "Recurrent Laryngeal Nerve Palsy", "nerve palsy recurrent laryngeal", "Vagus nerve laryngeal paralysis", "Vagus Nerve Laryngeal Paralysis", "recurrent laryngeal nerve palsy", "Laryngeal Nerve Palsy, Recurrent", "Laryngeal paralysis, vagus nerve", "PARALYSIS RECURRENT LARYNGEAL NERVE", "Paralysis recurrent laryngeal nerve", "Recurrent Laryngeal Nerve Paralysis", "Vagus nerve laryngeal paralysis (disorder)", "recurrent laryngeal nerve palsy (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Laryngeal Nerve Paralysis", "shortest_name_length": 31}
{"curie": "UMLS:C5446516", "names": ["Conjunctival Diffuse Large B-Cell Lymphoma", "Primary Conjunctival Diffuse Large B-Cell Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Conjunctival Diffuse Large B-Cell Lymphoma", "shortest_name_length": 42}
{"curie": "UMLS:C4520715", "names": ["stage I anal cancer", "Stage I Anal Canal Cancer", "Stage I Anal Canal Cancer AJCC v7", "Stage I Anal Canal Cancer AJCC v6", "Stage I Anal Carcinoma AJCC v6 and v7", "Stage I Anal Canal Cancer AJCC v6 and v7", "Stage I Anal Canal Carcinoma AJCC v6 and v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Anal Canal Cancer AJCC v6 and v7", "shortest_name_length": 19}
{"curie": "UMLS:C0154551", "names": ["Skin Disorder Arising from Mental Factor", "Skin disorder arising from mental factors"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Skin disorder arising from mental factors", "shortest_name_length": 40}
{"curie": "UMLS:C0333373", "names": ["Microabscess", "MICROABSCESS", "Microabscess (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Microabscess", "shortest_name_length": 12}
{"curie": "MONDO:0010605", "names": ["HEMOPOIETIC PROLIFERATION", "hemopoietic proliferation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hemopoietic proliferation", "shortest_name_length": 25}
{"curie": "UMLS:C0935909", "names": ["cutaneous breast cancer", "Cutaneous Breast Cancer", "Metastatic Breast Cancer in the Skin", "Breast Carcinoma Metastatic to the Skin", "Metastatic Breast Carcinoma in the Skin", "Breast Carcinoma Metastatic in the Skin"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Breast Carcinoma in the Skin", "shortest_name_length": 23}
{"curie": "MONDO:0017536", "names": ["mirror hand, bilateral", "central polydactyly of fingers, bilateral", "mesoaxial polydactyly of fingers, bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "central polydactyly of fingers, bilateral", "shortest_name_length": 22}
{"curie": "MONDO:0002145", "names": ["DSD", "CARD", "intersex", "Intersex", "Genital ambiguity", "Genital Ambiguity", "Ambiguity, Genital", "Atypical Genitalia", "Intersex genitalia", "ambiguous genitalia", "Intersex Conditions", "genitalia ambiguous", "Genital Ambiguities", "Ambiguous genitalia", "Ambiguous Genitalia", "intersex conditions", "Genitalia, Ambiguous", "Ambiguities, Genital", "sex development disorder", "Sex Development Disorder", "Sex Development Disorders", "genital organs; ambiguous", "Disorder of sex development", "Sexual Development Disorder", "sex differentiation disease", "disorder of sex development", "GENITALIA EXTERNAL AMBIGUOUS", "Genitalia external ambiguous", "Sexual Development Disorders", "Disorders of Sex Development", "disorders of sex development", "Ambiguous external genitalia", "sex differentiation disorder", "Sex Differentiation Disorder", "Sex Differentiation Disorders", "Differentiation Disorder, Sex", "Sex differentiation disorders", "Disorder, Sex Differentiation", "Ambiguous genitalia (disorder)", "disorder of sexual development", "Disorders, Sex Differentiation", "Differences of Sex Development", "differences of sex development", "Differentiation Disorders, Sex", "disorder of sex differentiation", "sexual differentiation disorder", "Disorders of Sexual Development", "Sexual Differentiation Disorder", "Disorder, Sexual Differentiation", "Sexual Differentiation Disorders", "Differentiation Disorder, Sexual", "Differentiation Disorders, Sexual", "Disorders, Sexual Differentiation", "Disorder of sexual differentiation", "disorder of sexual differentiation", "disorders of sex development (DSD)", "Disorder of Sexual Differentiation", "Ambiguous external genitalia at birth", "Disorder of sexual differentiation, NOS", "Conditions Affecting Reproductive Development", "Disorder of sexual differentiation (disorder)", "conditions affecting reproductive development"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "disorder of sexual differentiation", "shortest_name_length": 3}
{"curie": "UMLS:C5237417", "names": ["Locally Recurrent Merkel Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Locally Recurrent Merkel Cell Carcinoma", "shortest_name_length": 39}
{"curie": "MONDO:0007585", "names": ["EXT", "diaphyseal Aclasis", "osteochondromatosis", "multiple osteochondromas", "EXT1 exostoses, multiple", "exostoses, multiple, type 1", "exostoses, multiple, type I", "multiple cartilaginous exostoses", "exostoses, multiple caused by mutation in EXT1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exostoses, multiple, type 1", "shortest_name_length": 3}
{"curie": "UMLS:C0948160", "names": ["Pancreas infection", "infection pancreas", "pancreas infection", "infection; pancreas", "pancreas; infection", "infections pancreas", "Pancreatic Infection", "pancreatic infection", "pancreatic infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pancreatic Infection", "shortest_name_length": 18}
{"curie": "MONDO:0021583", "names": ["melanocytic skin neoplasm", "Skin Melanocytic Neoplasm", "Melanocytic Skin Neoplasm", "Melanocytic tumor of skin", "Melanocytic tumour of skin", "melanocytic neoplasm of skin", "Melanocytic Neoplasm of Skin", "Cutaneous Melanocytic Neoplasm", "cutaneous melanocytic neoplasm", "zone of skin melanocytic neoplasm", "melanocytic neoplasm of zone of skin", "Melanocytic tumor of skin (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "melanocytic skin neoplasm", "shortest_name_length": 25}
{"curie": "UMLS:C1336031", "names": ["Solitary Adult Fibroma", "Solitary Adult Skin Fibroma", "Solitary Adult Cutaneous Fibroma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Solitary Adult Fibroma", "shortest_name_length": 22}
{"curie": "MONDO:0022567", "names": ["bhaskar jagannathan syndrome", "Bhaskar Jagannathan syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bhaskar jagannathan syndrome", "shortest_name_length": 28}
{"curie": "MONDO:0015489", "names": ["predominantly medium-vessel vasculitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "predominantly medium-vessel vasculitis", "shortest_name_length": 38}
{"curie": "UMLS:C2363812", "names": ["Device intolerance"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Device intolerance", "shortest_name_length": 18}
{"curie": "MONDO:0004634", "names": ["venopathy", "Venopathy", "vein disease", "disease vein", "Vein disorder", "Vein Disorder", "diseases vein", "vein disorder", "disease veins", "VEIN DISORDER", "diseases veins", "veins diseases", "vein; disorder", "venous disease", "disorder veins", "disease venous", "disorders vein", "diseases venous", "disease of vein", "disorders veins", "Venous Disorder", "Disorder of vein", "disorder of vein", "disorder of veins", "Vein disorder NOS", "Disease of vein, NOS", "DISEASES OF THE VEINS", "Disorder of vein, NOS", "vein disease or disorder", "disease (or disorder); vein", "disease or disorder of vein", "Disorder of vein (disorder)", "disorder of vein (diagnosis)", "Disorder of vein, unspecified", "Other venous embolism & thrombosis", "Venous vascular disease or syndrome", "Other venous embolism and thrombosis", "Venous embolism and thrombosis, other"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vein disorder", "shortest_name_length": 9}
{"curie": "MONDO:0016865", "names": ["Kleefstra syndrome due to a point mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Kleefstra syndrome due to a point mutation", "shortest_name_length": 42}
{"curie": "UMLS:C1336366", "names": ["Stage IVB Esophageal Cancer", "Esophageal Cancer Stage IVB", "Stage IVB Esophagus Carcinoma", "Stage IVB Esophageal Carcinoma", "Stage IVB Carcinoma of Esophagus", "Stage IVB Carcinoma of the Esophagus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Esophageal Carcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0010999", "names": ["Bindewald Ulmer Muller syndrome", "Bindewald-Ulmer-Müller syndrome", "FALLOT complex with severe mental and growth retardation", "FALLOT COMPLEX WITH SEVERE MENTAL AND GROWTH RETARDATION", "Fallot complex with severe mental and growth retardation", "fallot complex-intellectual disability-growth delay syndrome", "Fallot complex-intellectual disability-growth delay syndrome", "Fallot complex with intellectual disability and growth delay syndrome", "Fallot complex with intellectual disability and growth delay syndrome (disorder)", "Fallot complex with intellectual disability and growth delay syndrome (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fallot complex-intellectual disability-growth delay syndrome", "shortest_name_length": 31}
{"curie": "MONDO:0009903", "names": ["GWAFD", "POADS", "POADS syndrome", "miller syndrome", "MILLER SYNDROME", "Miller syndrome", "millers syndrome", "miller syndromes", "miller's syndrome", "Miller's syndrome", "Postaxial acrodysostosis", "Genee-Wiedemann syndrome", "Wilm's aniridia syndrome", "postaxial acrodysostosis", "GENEE-WIEDEMANN SYNDROME", "genee-wiedemann syndrome", "Miller syndrome (disorder)", "Wildervanck-Smith syndrome", "POSTAXIAL ACROFACIAL DYSOSTOSIS", "Postaxial Acrofacial Dysostosis", "postaxial acrofacial dysostosis", "Postaxial acrofacial dysostosis", "Genee-Wiedemann acrofacial dysostosis", "Postaxial Acrofacial Dysostosis (POADS)", "Postaxial acrofacial dysostosis syndrome", "postaxial acrofacial dysostosis syndrome", "acrofacial dysostosis, Genee-Wiedmann type", "Acrofacial dysostosis, Genee-Wiedemann type", "Genee-Wiedemann acrofacial dysostosis (GWAFD)", "postaxial acrofacial dysostosis (POADS) syndrome", "Postaxial acrofacial dysostosis (POADS) syndrome", "mandibulfacial dysostosis with postaxial limb anomalies", "Mandibulfacial dysostosis with postaxial limb anomalies", "Mandibulofacial dysostosis with postaxial limb anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "postaxial acrofacial dysostosis", "shortest_name_length": 5}
{"curie": "MONDO:0017257", "names": ["idiopathic posterior uveitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "idiopathic posterior uveitis", "shortest_name_length": 28}
{"curie": "MONDO:0022417", "names": ["Alopecia congenita keratosis palmoplantaris", "alopecia congenita keratosis palmoplantaris", "alopecia congenita with keratosis palmoplantaris", "Alopecia Congenita With Keratosis Palmoplantaris", "Alopecia congenita with hyperkeratosis of the palms and soles", "alopecia congenita with hyperkeratosis of the palms and soles"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "alopecia congenita keratosis palmoplantaris", "shortest_name_length": 43}
{"curie": "MONDO:0100456", "names": ["neonatal encephalopathy with non-epileptic myoclonus"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal encephalopathy with non-epileptic myoclonus", "shortest_name_length": 52}
{"curie": "MONDO:0003905", "names": ["glandular pattern ovarian yolk sac tumor", "Ovarian Yolk Sac Tumor, Glandular Pattern", "ovarian yolk sac tumor, glandular pattern", "ovarian yolk Sac tumor, glandular pattern"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian yolk sac tumor, glandular pattern", "shortest_name_length": 40}
{"curie": "MONDO:0017813", "names": ["Van Maldergem syndrome", "van Maldergem syndrome", "cerebro-facio-articular syndrome", "Van Maldergem Wetzburger Verloes syndrome", "cerebro-facio-articular syndrome of Van Maldergem"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "van Maldergem syndrome", "shortest_name_length": 22}
{"curie": "MONDO:0044328", "names": ["SRTD20", "SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY", "short-rib thoracic dysplasia 20 with polydactyly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "short-rib thoracic dysplasia 20 with polydactyly", "shortest_name_length": 6}
{"curie": "UMLS:C4525434", "names": ["Ampulla of Vater Cancer by AJCC v7 Stage", "Ampulla of Vater Carcinoma by AJCC v7 Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ampulla of Vater Cancer by AJCC v7 Stage", "shortest_name_length": 40}
{"curie": "MONDO:0014793", "names": ["MCCPD", "smo deficiency", "SMO deficiency", "Sc4Mol deficiency", "SC4MOL DEFICIENCY", "Sterol-C4-methyl oxidase deficiency", "sterol-C4-methyl oxidase deficiency", "SMO (sterol-C4-methyl oxidase) deficiency", "microcephaly, congenital cataract, and psoriasiform dermatitis", "MICROCEPHALY, CONGENITAL CATARACT, AND PSORIASIFORM DERMATITIS", "MICROCEPHALY, CONGENITAL CATARACTS, AND PSORIASIFORM DERMATITIS", "microcephaly-congenital cataract-psoriasiform dermatitis syndrome", "Microcephaly-congenital cataract-psoriasiform dermatitis syndrome", "Microcephaly, congenital cataract, psoriasiform dermatitis syndrome", "Microcephaly, congenital cataract, psoriasiform dermatitis syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly-congenital cataract-psoriasiform dermatitis syndrome", "shortest_name_length": 5}
{"curie": "MONDO:0015832", "names": ["true unicornuate uterus", "complete unilateral Mullerian aplasia", "complete unilateral Müllerian aplasia", "unicornuate uterus without rudimentary horn", "complete unilateral aplasia of the Müllerian ducts", "complete unilateral aplasia of the Mullerian ducts"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "true unicornuate uterus", "shortest_name_length": 23}
{"curie": "MONDO:0016619", "names": ["AR-HED", "Autosomal Recessive Anhidrotic Ectodermal Dysplasia", "Autosomal Recessive Anhydrotic Ectodermal Dysplasia", "autosomal recessive anhidrotic ectodermal dysplasia", "Autosomal recessive anhidrotic ectodermal dysplasia", "Anhydridic Ectodermal Dysplasia, Autosomal Recessive", "Anhidrotic Ectodermal Dysplasia, Autosomal Recessive", "Anhidridic Ectodermal Dysplasia, Autosomal Recessive", "anhidrotic ectodermal dysplasia, autosomal recessive", "Hypohidrotic autosomal recessive ectodermal dysplasia", "Autosomal Recessive Hypohidrotic Ectodermal Dysplasia", "hypohidrotic ectodermal dysplasia autosomal recessive", "autosomal recessive hypohidrotic ectodermal dysplasia", "Ectodermal Dysplasia, Anhidrotic, Autosomal Recessive", "Autosomal recessive hypohidrotic ectodermal dysplasia", "hypohidrotic ectodermal dysplasia, autosomal recessive", "Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive", "Ectodermal Dysplasia, Hypohydrotic, Autosomal Recessive", "Autosomal recessive hypohidrotic ectodermal dysplasia syndrome", "Hypohidrotic ectodermal dysplasia syndrome, autosomal recessive type", "Autosomal recessive hypohidrotic ectodermal dysplasia syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive hypohidrotic ectodermal dysplasia", "shortest_name_length": 6}
{"curie": "MONDO:0011086", "names": ["SCID due to complete RAG1/2 deficiency", "SCID due to complete RAG1-2 deficiency", "severe combined immunodeficiency, B cell-negative", "SCID, T Cell-Negative, B Cell-Negative, NK Cell-Positive", "SCID, T cell-negative, B cell-negative, NK cell-positive", "SCID, T CELL-NEGATIVE, B CELL-NEGATIVE, NK CELL-POSITIVE", "SCID, AR, T-cell negative, B-cell negative, NK cell-positive", "Severe combined immunodeficiency due to complete RAG1-2 deficiency", "severe combined immunodeficiency due to complete RAG1-2 deficiency", "severe combined immunodeficiency due to complete RAG1/2 deficiency", "autosomal recessive T cell-negative, B-cell negative, NK cell-positive SCID", "severe immunodeficiency, autosomal recessive, T-cell negative, B-cell negative, NK cell-positive", "SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-NEGATIVE, NK CELL-POSITIVE", "severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive", "severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, Nk cell-positive", "Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, NK Cell-Positive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive", "shortest_name_length": 38}
{"curie": "UMLS:C5237248", "names": ["Unresectable Acral Melanoma", "Unresectable Acral Lentiginous Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Acral Lentiginous Melanoma", "shortest_name_length": 27}
{"curie": "MONDO:0007474", "names": ["duodenal ulcer due to antral G-cell hyperfunction", "Duodenal ulcer due to antral G-cell hyperfunction", "DUODENAL ULCER DUE TO ANTRAL G-CELL HYPERFUNCTION", "hypergastrinemic, hyperpepsinogenemic duodenal ulcer", "Hypergastrinemic, hyperpepsinogenemic duodenal ulcer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "duodenal ulcer due to antral G-cell hyperfunction", "shortest_name_length": 49}
{"curie": "UMLS:C3495549", "names": ["PATENT DUCTUS ARTERIOSUS", "DUCTUS ARTERIOSUS PATENT", "Ductus arteriosus patent", "patent ductus arteriosus", "Patent ductus arteriosus", "Persistent ductus arteriosus", "Patent ductus arteriosus - persisting type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Patent ductus arteriosus - persisting type", "shortest_name_length": 24}
{"curie": "MONDO:0007505", "names": ["earlobe sinuses", "EARLOBE SINUSES", "EARRING HOLES, NATURAL", "earring holes, natural"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "earring holes, natural", "shortest_name_length": 15}
{"curie": "UMLS:C4725815", "names": ["Refractory Malignant Thyroid Gland Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Malignant Thyroid Gland Neoplasm", "shortest_name_length": 43}
{"curie": "UMLS:C3831087", "names": ["Class 2 Uveal Melanoma", "Uveal Class 2 Melanoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Uveal Class 2 Melanoma", "shortest_name_length": 22}
{"curie": "UMLS:C1335702", "names": ["Recurrent Digestive System Carcinoma", "Recurrent Gastrointestinal System Cancer", "Recurrent Gastrointestinal System Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Digestive System Carcinoma", "shortest_name_length": 36}
{"curie": "MONDO:0009122", "names": ["DOHLE BODIES AND LEUKEMIA", "Dohle Bodies and Leukemia", "Dohle bodies and leukemia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Dohle bodies and leukemia", "shortest_name_length": 25}
{"curie": "MONDO:0018976", "names": ["Schisis association", "schisis association", "Schisis association syndrome", "Midline development field defects", "Schisis association syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schisis association", "shortest_name_length": 19}
{"curie": "MONDO:0009164", "names": ["LYON SYNDROME", "Lyon syndrome", "encephalopathy, axonal, with necrotizing myopathy, cardiomyopathy, and cataracts", "Encephalopathy, Axonal, with Necrotizing Myopathy, Cardiomyopathy, and Cataracts", "ENCEPHALOPATHY, AXONAL, WITH NECROTIZING MYOPATHY, CARDIOMYOPATHY, AND CATARACTS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephalopathy, axonal, with necrotizing myopathy, cardiomyopathy, and cataracts", "shortest_name_length": 13}
{"curie": "MONDO:0044986", "names": ["lymphoid system disease", "lymphoid system disorder", "disease of lymphoid system", "disorder of lymphoid system", "lymphoid system disease or disorder", "disease or disorder of lymphoid system"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lymphoid system disorder", "shortest_name_length": 23}
{"curie": "MONDO:0022872", "names": ["corpus callosum dysgenesis X-linked recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corpus callosum dysgenesis X-linked recessive", "shortest_name_length": 45}
{"curie": "UMLS:C1336388", "names": ["Stage IVB Osteosarcoma", "Stage IVB Osteogenic Sarcoma", "Stage IVB Osteosarcoma AJCC v7", "Stage IVB Osteosarcoma  AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVB Osteosarcoma AJCC v7", "shortest_name_length": 22}
{"curie": "UMLS:C0279178", "names": ["stage III follicular thyroid cancer", "thyroid cancer, stage III follicular", "follicular thyroid cancer, stage III", "Stage III Thyroid Follicular Carcinoma", "Stage III Thyroid Gland Follicular Cancer", "carcinoma, follicular, thyroid, stage III", "Stage III Follicular Carcinoma of Thyroid", "Stage III Thyroid Gland Follicular Carcinoma", "Stage III Follicular Thyroid Gland Carcinoma", "Stage III Follicular Carcinoma of the Thyroid", "follicular carcinoma of the thyroid, stage III", "Stage III Follicular Carcinoma of Thyroid Gland", "Stage III Follicular Carcinoma of the Thyroid Gland", "Stage III Thyroid Gland Follicular Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Thyroid Gland Follicular Carcinoma AJCC v7", "shortest_name_length": 35}
{"curie": "UMLS:C0729524", "names": ["Bacterial urinary infection", "bacterial urinary tract infection", "urinary tract infection bacterial", "Urinary tract infection bacterial", "Bacterial urinary infection (disorder)", "Bacterial UTI (urinary tract infection)", "bacterial urinary tract infection (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Bacterial urinary infection", "shortest_name_length": 27}
{"curie": "UMLS:C5206378", "names": ["Advanced Lung Non-Small Cell Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Lung Non-Small Cell Carcinoma", "shortest_name_length": 38}
{"curie": "MONDO:0018689", "names": ["PCL", "Plasma Cell Leukemia", "PLASMA CELL LEUKEMIA", "Plasmacytic Leukemia", "Plasma cell leukemia", "leukemia plasmacytic", "LEUKEMIA PLASMACYTIC", "LEUKEMIA PLASMA CELL", "Leukemia plasmacytic", "Plasmacytic leukemia", "Leukemia Plasmacytic", "plasmacytic leukemia", "plasma cell leukemia", "plasmacytic leukaemia", "LEUKEMIA, PLASMACYTIC", "Leukemia, Plasmacytic", "LEUKEMIA, PLASMA CELL", "leukemia, plasma cell", "Plasma cell leukaemia", "Leukaemia plasmacytic", "leukemia; plasma cell", "cells leukemia plasma", "plasma cell; leukemia", "Plasmacytic leukaemia", "Leukemia, Plasma Cell", "plasma cell leukaemia", "Plasmacytic Leukemias", "Plasma Cell Leukemias", "Leukemias, Plasmacytic", "Leukemias, Plasma Cell", "[M]Plasma cell leukemia", "Plasma cell leukemia NOS", "[M]Plasma cell leukaemia", "Plasma cell leukemia, disease", "Plasma cell leukaemia, disease", "Plasma cell leukemia, morphology", "plasma cell leukemia (diagnosis)", "Plasma cell leukaemia, morphology", "Plasma cell leukemia, disease (disorder)", "Plasma cell leukemia, morphology (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "plasma cell leukemia", "shortest_name_length": 3}
{"curie": "MONDO:0100161", "names": ["type 4 RTA", "hyperkalemic RTA", "renal tubular acidosis type 4", "type 4 renal tubular acidosis", "hyperkalemic renal tubular acidosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hyperkalemic renal tubular acidosis", "shortest_name_length": 10}
{"curie": "UMLS:C0679048", "names": ["Obsessive thoughts", "Obsessive Thinking", "obsessive thoughts", "obsessive thinking"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Obsessive thoughts", "shortest_name_length": 18}
{"curie": "MONDO:0015275", "names": ["PAVC", "Partial AVSD", "partial AVSD", "partial; AVSD", "AVSD; partial", "Septum primum defect", "partial AV septal defect", "Primum atrial septal defect", "Partial atrioventricular canal", "partial atrioventricular canal", "Atrioventricular canal, partial", "Atrial septal defect, primum-type", "Atrial septal defect, primum type", "ATRIAL SEPTAL DEFECT, PRIMUM TYPE", "Atrial Septal Defect, Primum Type", "ASD1 - Primum atrial septal defect", "ASD I - Primum atrial septal defect", "1 ASD - Primum atrial septal defect", "Primum atrioventricular canal defect", "partial atrioventricular canal defect", "Partial common atrioventricular canal", "Partial atrioventricular canal defect", "partial common atrioventricular canal", "partial atrioventricular septal defect", "Atrioventricular canal defect, partial", "Partial atrioventricular septal defect", "Atrioventricular septal defect, partial", "partial atrioventricular septal defects", "Partial atrioventricular septal defects", "Partial defect of atrioventricular canal", "partial atrioventricular canal (diagnosis)", "partial atrioventricular septal defect (diagnosis)", "Partial defect of atrioventricular canal (disorder)", "Atrioventricular septal defect - isolated atrial component", "Atrioventricular septal defect - isolated atrial component (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial atrioventricular canal", "shortest_name_length": 4}
{"curie": "UMLS:C0456087", "names": ["Fetal asphyxia", "Fetal Asphyxia", "asphyxia; fetal", "fetal; asphyxia", "In Utero Asphyxia", "Antepartum fetal asphyxia", "Antepartum foetal asphyxia", "intrauterine asphyxia antepartum", "Antepartum fetal asphyxia (disorder)", "Antepartum fetal asphyxia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Antepartum fetal asphyxia", "shortest_name_length": 14}
{"curie": "MONDO:0000082", "names": ["Urogenital prolapse", "Urogenital Prolapse", "Prolapse, Urogenital", "Urogenital Prolapses", "pelvic organ prolapse", "Pelvic Organ Prolapse", "Prolapses, Urogenital", "Pelvic organ prolapse", "Organ Prolapse, Pelvic", "Prolapse, Pelvic Organ", "Vaginal Vault Prolapse", "Pelvic Organ Prolapses", "vaginal vault prolapse", "Vaginal vault prolapse", "prolapse vaginal vault", "Vaginal Vault Prolapses", "Prolapse, Vaginal Vault", "Vault Prolapse, Vaginal", "Prolapses, Pelvic Organ", "Organ Prolapses, Pelvic", "Prolapses, Vaginal Vault", "Vault Prolapses, Vaginal", "Bulge of the vaginal vault", "Vaginal vault prolapse (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pelvic organ prolapse", "shortest_name_length": 19}
{"curie": "MONDO:0003412", "names": ["retroperitoneal hemangiopericytoma", "Retroperitoneal Hemangiopericytoma", "retroperitoneal space hemangiopericytoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retroperitoneal hemangiopericytoma", "shortest_name_length": 34}
{"curie": "UMLS:C1336157", "names": ["Stage IIA Endometrial Cancer AJCC v6", "Stage IIA Uterine Corpus Cancer AJCC v6", "Stage IIA Uterine (including Endometrial) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIA Uterine Corpus Cancer AJCC v6", "shortest_name_length": 36}
{"curie": "UMLS:C4682752", "names": ["IIIA", "Stage IIIA Prostate Cancer", "stage IIIA prostate cancer", "Stage IIIA Prostate Cancer AJCC v8", "stage IIIA prostate cancer AJCC v8", "stage IIIA prostate carcinoma AJCC v8", "Stage IIIA Prostate Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Prostate Cancer AJCC v8", "shortest_name_length": 4}
{"curie": "MONDO:0004993", "names": ["Carcinoma", "carcinoma", "CARCINOMA", "carcinomas", "Carcinomas", "EPITHELIOMA", "epithelioma", "Epithelioma", "epitheliomas", "Epitheliomas", "Carcinoma NOS", "Carcinoma, NOS", "Other Carcinoma", "Other carcinoma", "Epithelioma, NOS", "epithelial cancer", "epithelial carcinoma", "carcinoma, malignant", "Epithelial Carcinoma", "CARCINOMA, MALIGNANT", "Epithelioma Malignant", "Malignant epithelioma", "malignant epithelioma", "malignant Epithelioma", "Malignant Epithelioma", "epithelioma malignant", "carcinoma (diagnosis)", "Epithelioma, malignant", "malignant epithelial tumor", "Malignant Epithelial Tumor", "Malignant epithelial tumor", "Tumor, Malignant Epithelial", "Epithelial Tumor, Malignant", "Epithelial tumor, malignant", "Malignant Epithelial Tumors", "Malignant epithelial tumour", "Epithelial tumour, malignant", "Epithelial Tumors, Malignant", "malignant epithelial neoplasm", "Malignant Epithelial Neoplasm", "Malignant epithelial neoplasm", "Malignant Epithelial Neoplasms", "Epithelial Neoplasm, Malignant", "Neoplasm, Malignant Epithelial", "Epithelial Neoplasms, Malignant", "Neoplasms, Malignant Epithelial", "malignant epithelioma (diagnosis)", "Carcinoma (morphologic abnormality)", "Malignant epithelial neoplasm (disorder)", "unspecified site; carcinoma, unspecified site", "carcinoma; unspecified site, unspecified site", "Epithelioma, malignant (morphologic abnormality)", "Malignant epithelial neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "carcinoma", "shortest_name_length": 9}
{"curie": "MONDO:0012106", "names": ["MCPH5", "primary autosomal recessive microcephaly 5", "Microcephaly, Primary Autosomal Recessive, 5", "MICROCEPHALY 5, PRIMARY, AUTOSOMAL RECESSIVE", "microcephaly 5, primary, autosomal recessive", "ASPM autosomal recessive primary microcephaly", "autosomal recessive primary microcephaly caused by mutation in ASPM"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microcephaly 5, primary, autosomal recessive", "shortest_name_length": 5}
{"curie": "UMLS:C1336721", "names": ["testicular yolk sac tumor and teratoma", "testicular teratoma and yolk sac tumor", "yolk sac tumor and teratoma, testicular", "teratoma and yolk sac tumor of the testis", "testis cancer, yolk sac tumor and teratoma", "testis cancer, teratoma and yolk sac tumor", "Mixed Yolk Sac Tumor and Teratoma of Testis", "testicle cancer, teratoma and yolk sac tumor", "Testicular Mixed Yolk Sac Tumor and Teratoma", "testicular cancer, yolk sac tumor and teratoma", "testicular cancer, teratoma and yolk sac tumor", "Mixed Yolk Sac Neoplasm and Teratoma of Testis", "Mixed Yolk Sac Tumor and Teratoma of the Testis", "Testicular Mixed Yolk Sac Neoplasm and Teratoma", "Mixed Yolk Sac Neoplasm and Teratoma of the Testis", "Mixed Endodermal Sinus Tumor and Teratoma of Testis", "Testicular Mixed Endodermal Sinus Tumor and Teratoma", "Mixed Endodermal Sinus Neoplasm and Teratoma of Testis", "Mixed Endodermal Sinus Tumor and Teratoma of the Testis", "Testicular Mixed Endodermal Sinus Neoplasm and Teratoma", "Mixed Endodermal Sinus Neoplasm and Teratoma of the Testis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Testicular Mixed Yolk Sac Tumor and Teratoma", "shortest_name_length": 38}
{"curie": "MONDO:0003177", "names": ["prostate adenoid cystic carcinoma", "Prostate Adenoid Cystic Carcinoma", "adenoid cystic carcinoma of prostate", "Adenoid Cystic Carcinoma of Prostate", "prostate gland adenoid cystic carcinoma", "Adenoid Cystic Carcinoma of the Prostate", "adenoid cystic carcinoma of the prostate"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "prostate adenoid cystic carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0016812", "names": ["DRD", "DYT5", "DYT5a", "DYSTONIA 5", "Dystonia 5", "DYT5 Dystonia", "DYT5 dystonia", "Segawa dystonia", "DYT-TH (subtype)", "Segawa's disease", "Diurnal dystonia", "Segawa's Disease", "Diurnal Dystonia", "DYT-SPR (subtype)", "Dystonia, Diurnal", "DYT-GCH1 (subtype)", "GTPCH1-deficient DRD", "Dopa-responsive dystonia", "dopa-responsive dystonia", "Dopa responsive dystonia", "Dopa-Responsive Dystonia", "DYSTONIA, DOPA-RESPONSIVE", "Dystonia, Dopa-responsive", "Diurnal dystonia (disorder)", "HPD with diurnal fluctuation", "Levodopa-responsive dystonia", "Autosomal dominant Segawa syndrome", "HPD with marked diurnal fluctuation", "Segawa syndrome, autosomal dominant", "SEGAWA SYNDROME, AUTOSOMAL DOMINANT", "GTPCH1-deficient dopa-responsive dystonia", "Autosomal dominant dopa-responsive dystonia", "Autosomal dominant dopa responsive dystonia", "Dopa-responsive dystonia, autosomal dominant", "DOPA-RESPONSIVE DYSTONIA, AUTOSOMAL DOMINANT", "Dystonia, Dopa-responsive, autosomal dominant", "DYSTONIA, DOPA-RESPONSIVE, AUTOSOMAL DOMINANT", "DYSTONIA, PROGRESSIVE, WITH DIURNAL VARIATION", "Dystonia, progressive, with diurnal variation", "DYSTONIA-PARKINSONISM WITH DIURNAL FLUCTUATION", "Dystonia-Parkinsonism with diurnal fluctuation", "Autosomal dominant dopa responsive dystonia (disorder)", "hereditary progressive dystonia with diurnal fluctuation", "Hereditary progressive dystonia with diurnal fluctuation", "Hereditary Progressive Dystonia with Marked Diurnal Fluctuation", "Hereditary progressive dystonia with marked diurnal fluctuation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dopa-responsive dystonia", "shortest_name_length": 3}
{"curie": "MONDO:0001566", "names": ["Hypercalcemia", "HYPERCALCEMIA", "hypercalcemia", "Hypercalcaemia", "HYPERCALCAEMIA", "hypercalcaemia", "Hypercalcemias", "hypercalcinemia", "hypercalcemia disease", "Hypercalcemia syndrome", "Hypercalcemic disorder", "CALCIUM BLOOD INCREASED", "Calcium blood increased", "Hypercalcaemia syndrome", "Blood calcium increased", "Hypercalcemia (disorder)", "hypercalcemia (diagnosis)", "High blood calcium levels", "Raised serum calcium level", "Increased calcium in blood", "Serum calcium concentration above normal", "Serum calcium level above reference range", "Serum calcium level above reference range (finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypercalcemia disease", "shortest_name_length": 13}
{"curie": "UMLS:C5446573", "names": ["Optic Nerve Sheath Solitary Fibrous Tumor", "Solitary Fibrous Tumor of the Optic Nerve Sheath", "Solitary Fibrous Tumor/Hemangiopericytoma of the Optic Nerve Sheath"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Optic Nerve Sheath Solitary Fibrous Tumor", "shortest_name_length": 41}
{"curie": "UMLS:C0519097", "names": ["LV wall aneurysmal", "left aneurysm ventricular", "Left ventricular aneurysm", "left ventricular aneurysm", "Left Ventricular Aneurysm", "LEFT VENTRICULAR ANEURYSM", "VENTRICULAR ANEURYSM LEFT", "aneurysms left ventricular", "aneurysm of left ventricle", "LVA - Left ventricular aneurysm", "Left ventricular wall aneurysmal", "Left ventricular aneurysm (disorder)", "aneurysm of left ventricle (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Left ventricular aneurysm", "shortest_name_length": 18}
{"curie": "MONDO:0032658", "names": ["MACID", "MACROCEPHALY, ACQUIRED, WITH MENTAL RETARDATION", "Macrocephaly, Acquired, With Mental Retardation", "macrocephaly, acquired, with impaired intellectual development", "MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "macrocephaly, acquired, with impaired intellectual development", "shortest_name_length": 5}
{"curie": "UMLS:C3900095", "names": ["Pleomorphic Hepatocellular Cancer", "Adult Pleomorphic Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Pleomorphic Hepatocellular Carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0002178", "names": ["Deciduoma", "Deciduomas", "Placenta Tumor", "placenta cancer", "Placental Tumor", "Placenta Tumors", "placental tumors", "Placental tumors", "placental cancer", "Placental Tumors", "Placenta Neoplasm", "placenta neoplasm", "Tumor of Placenta", "Placental neoplasm", "Placenta Neoplasms", "cancer of placenta", "Placental Neoplasm", "placental neoplasm", "Placental neoplasms", "Neoplasm of placenta", "DECIDUOMA, MALIGNANT", "Neoplasm of Placenta", "neoplasm of placenta", "deciduoma, malignant", "Tumor of the Placenta", "Placental neoplasm NOS", "Neoplasm malig;placenta", "Neoplasm of the Placenta", "malignant placenta tumor", "Malignant Placenta Tumor", "malignant Placental tumor", "Malignant Placental Tumor", "malignant placental tumor", "malignant tumor of placenta", "Malignant Placenta Neoplasm", "Malignant Tumor of Placenta", "malignant placenta neoplasm", "Malignant Placental Neoplasm", "malignant placental neoplasm", "Malignant neoplasm of placenta", "malignant neoplasm of placenta", "Malignant Neoplasm of Placenta", "Malignant Tumor of the Placenta", "malignant tumor of the placenta", "Neoplasm of placenta (disorder)", "neoplasm of placenta (diagnosis)", "Malignant Neoplasm of the Placenta", "malignant neoplasm of the placenta", "malignant neosplasm of the placenta", "primary malignant neoplasm of placenta", "malignant neoplasm of placenta (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "placenta cancer", "shortest_name_length": 9}
{"curie": "UMLS:C3263719", "names": ["PAM", "C-MIN", "PAM with Atypia", "Primary acquired melanosis", "Conjunctival Melanoma In Situ", "Conjunctival Premalignant Melanosis", "Conjunctival Precancerous Melanosis", "Conjunctival primary acquired melanosis", "Conjunctival Primary Acquired Melanosis", "Primary acquired melanosis of conjunctiva", "PAM - Primary acquired melanosis of conjunctiva", "Primary acquired melanocytic nevus of conjunctiva", "Primary acquired melanocytic naevus of conjunctiva", "Conjunctival Melanocytic Intraepithelial Neoplasia", "Primary acquired melanocytic nevus of conjunctiva (disorder)", "Conjunctival Primary Acquired Melanosis with Atypia/Melanoma In Situ", "Conjunctival Melanocytic Intraepithelial Neoplasia (C-MIN Score of 2-4)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary acquired melanosis", "shortest_name_length": 3}
{"curie": "UMLS:C1335915", "names": ["G3 Grade 3", "Sarcoma FNCLCC Grade 3", "FNCLCC Sarcoma Grade 3", "Sarcoma Differentiation Score 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FNCLCC Sarcoma Grade 3", "shortest_name_length": 10}
{"curie": "MONDO:0021079", "names": ["Neoplasm", "Childhood Tumor", "pediatric tumor", "childhood tumor", "Pediatric Tumor", "pediatric neoplasm", "childhood neoplasm", "Childhood Neoplasm", "Pediatric Neoplasm", "pediatric neoplasm (disease)", "childhood neoplasm (disease)", "neoplasm (disease) of childhood"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "childhood neoplasm", "shortest_name_length": 8}
{"curie": "UMLS:C4553703", "names": ["Stage IV Ovarian Cancer", "Stage IV Ovarian Cancer AJCC v8", "Stage IV Ovarian Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Ovarian Cancer AJCC v8", "shortest_name_length": 23}
{"curie": "UMLS:C4684862", "names": ["Recurrent Rhabdoid Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Rhabdoid Tumor", "shortest_name_length": 24}
{"curie": "MONDO:0000303", "names": ["Conidiobolomycosis", "conidiobolomycosis", "Conidiobolus infection", "infection; conidiobolus", "Conidiobolus; infection", "infection by Conidiobolus", "rhinoentomophthoromycosis", "Infection by Conidiobolus", "Rhinoentomophthoromycosis", "Conidiobolomycosis (disorder)", "Infection by Conidiobolus, NOS", "Conidiobolus infectious disease"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "conidiobolomycosis", "shortest_name_length": 18}
{"curie": "MONDO:0700075", "names": ["congenital muscular dystrophy-POMGNT2 related", "congenital muscular dystrophy caused by mutation in POMGNT2", "congenital muscular dystrophy caused by variation in POMGNT2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital muscular dystrophy caused by variation in POMGNT2", "shortest_name_length": 45}
{"curie": "UMLS:C4055221", "names": ["Clostridium sordellii Colitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Clostridium sordellii Colitis", "shortest_name_length": 29}
{"curie": "UMLS:C1735864", "names": ["Administration site infection"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Administration site infection", "shortest_name_length": 29}
{"curie": "UMLS:C4330338", "names": ["Hyperinsulinism in the Infant of a Diabetic Mother"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hyperinsulinism in the Infant of a Diabetic Mother", "shortest_name_length": 50}
{"curie": "MONDO:0012032", "names": ["Braddock syndrome", "Braddock syndrome (disorder)", "VATER-like syndrome with pulmonary hypertension, abnormal ear and growth deficiency", "Vater-like syndrome with pulmonary hypertension, abnormal ears and growth deficiency", "Vater-Like Defects with Pulmonary Hypertension, Laryngeal Webs, and Growth Deficiency", "VATER-like defects with pulmonary hypertension, laryngeal webs, and growth deficiency", "VATER-LIKE DEFECTS WITH PULMONARY HYPERTENSION, LARYNGEAL WEBS, AND GROWTH DEFICIENCY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Braddock syndrome", "shortest_name_length": 17}
{"curie": "MONDO:0054582", "names": ["TBS2", "TOWNES-BROCKS SYNDROME 2", "Townes-Brocks syndrome 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Townes-Brocks syndrome 2", "shortest_name_length": 4}
{"curie": "UMLS:C1514226", "names": ["Sertoli-Leydig cell tumor, poorly differentiated, with heterologous elements", "Poorly Differentiated Ovarian Sertoli-Leydig Cell Tumor, Variant with Heterologous Elements"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Poorly Differentiated Ovarian Sertoli-Leydig Cell Tumor, Variant with Heterologous Elements", "shortest_name_length": 76}
{"curie": "MONDO:0014599", "names": ["MRD34", "autosomal dominant mental retardation 34", "mental retardation, autosomal dominant 34", "MENTAL RETARDATION, AUTOSOMAL DOMINANT 34", "autosomal dominant intellectual disability 34", "intellectual disability, autosomal dominant 34", "mental retardation, autosomal dominant type 34", "intellectual disability, autosomal dominant type 34", "autosomal dominant intellectual developmental disorder 34", "intellectual developmental disorder, autosomal dominant 34", "INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 34", "autosomal dominant non-syndromic intellectual disability 34", "COL4A3BP autosomal dominant non-syndromic intellectual disability", "autosomal dominant non-syndromic intellectual disability caused by mutation in COL4A3BP"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, autosomal dominant 34", "shortest_name_length": 5}
{"curie": "MONDO:0018582", "names": ["GCHN", "MVAH", "MAHVASH DISEASE", "Mahvash disease", "Mahvash Disease", "Mahvash Syndrome", "GCGR-related hyperglucagonemia", "GCGR-related hyperglucagonaemia", "Glucagon Cell Hyperplasia and Neoplasia", "alpha-cell hyperplasia with glucagonemia", "ALPHA-CELL HYPERPLASIA WITH GLUCAGONEMIA", "Glucagon receptor-related hyperglucagonemia", "Glucagon receptor-related hyperglucagonaemia", "Glucagon receptor-related hyperglucagonemia (disorder)", "nesidioblastosis alpha cell hyperplasia microglucagonoma and nonfunctioning islet cell tumor", "nesidioblastosis, alpha cell hyperplasia, microglucagonoma, and nonfunctioning islet cell tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "GCGR-related hyperglucagonemia", "shortest_name_length": 4}
{"curie": "MONDO:0014645", "names": ["BENTA", "BENTA disease", "CARD 11/BENTA", "B-Cell Expansion with NFKB and T-Cell Anergy", "B-cell expansion with NFKB and T-cell anergy", "B-CELL EXPANSION WITH NFKB AND T-CELL ANERGY", "B-cell expansion with NF-kB and T-cell anergy disease", "B-cell expansion with nuclear factor kappa light chain enhancer of activated B cells and T-cell anergy disease", "BENTA (B-cell expansion with nuclear factor kappa light chain enhancer of activated B cells and T-cell anergy) disease", "B-cell expansion with nuclear factor kappa light chain enhancer of activated B cells and T-cell anergy disease (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "BENTA disease", "shortest_name_length": 5}
{"curie": "UMLS:C4524645", "names": ["Esophageal Squamous Cell Carcinoma by AJCC v8 pTNM Stage", "Esophageal Squamous Cell Carcinoma Tumor Stage Pathologic", "Esophageal Squamous Cell Carcinoma by AJCC v8 Pathologic Stage"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Esophageal Squamous Cell Carcinoma by AJCC v8 Pathologic Stage", "shortest_name_length": 56}
{"curie": "UMLS:C0743668", "names": ["Limb injury", "limb injury", "Injury;limb", "Limb Injury", "injury limbs", "limb; injury", "injury; limb", "injuries limb", "Limb injury NOS", "extremity injury", "EXTREMITY INJURY", "Injury-extremity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Limb injury", "shortest_name_length": 11}
{"curie": "UMLS:C0205649", "names": ["Monomorphic adenoma", "monomorphic adenoma", "Monomorphic Adenoma", "Monomorphic Adenomas", "Adenoma, Monomorphic", "Adenomas, Monomorphic", "Salivary Gland Monomorphic Adenoma", "Monomorphic adenoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adenoma, Monomorphic", "shortest_name_length": 19}
{"curie": "MONDO:0004785", "names": ["TARSITIS", "tarsitis", "BLEPHARITIS", "blepharitis", "Blepharitis", "Blepharitides", "Blepharitis, NOS", "cellulitis; eyelid", "eyelid; cellulitis", "EYELID INFLAMMATION", "eyelid inflammation", "Ciliary blepharitis", "Inflammation;eyelid", "Eyelid inflammation", "inflammation eyelids", "Cellulitis of eyelid", "cellulitis of eyelid", "inflammation; eyelid", "Marginal blepharitis", "eyelid; inflammation", "Cellulitis of eyelids", "inflammation of eyelid", "Inflammation of eyelid", "Blepharitis (disorder)", "Unspecified blepharitis", "blepharitis (diagnosis)", "Inflammation of eyelids", "Blepharitis, unspecified", "Inflammation of lid margin", "inflammation of the eyelid", "Inflammation of eyelid NOS", "Inflammation of eyelid, NOS", "Cellulitis of eyelid (disorder)", "eyelid inflammation (diagnosis)", "Inflammation of eyelid (disorder)", "Unspecified inflammation of eyelid", "Inflammation of eyelid, unspecified", "cellulitis of eyelid (physical finding)", "Infective dermatitis of eyelid of types resulting in deformity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blepharitis", "shortest_name_length": 8}
{"curie": "MONDO:0004824", "names": ["Neonatal thrush", "Neonatal monilia", "Neonatal moniliasis", "Neonatal candidosis", "neonatal moniliasis", "Neonatal candidiasis", "neonatal; moniliasis", "moniliasis; neonatal", "neonatal candidiasis", "Neonatal Candidiasis", "candidiasis; neonatal", "neonatal; candidiasis", "neonatal Monilia infection", "Neonatal Candida infection", "neonatal candida infection", "neonatal Candida infection", "Neonatal monilia infection", "Neonatal candida infection", "infection; monilia, neonatal", "candida; infection, neonatal", "infection; Candida, neonatal", "monilia; infection, neonatal", "Neonatal candidiasis (disorder)", "neonatal candidiasis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neonatal candidiasis", "shortest_name_length": 15}
{"curie": "MONDO:0008202", "names": ["PAROTIDOMEGALY, HEREDITARY BILATERAL", "Parotidomegaly, hereditary bilateral", "Parotidomegaly, Hereditary Bilateral"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parotidomegaly, hereditary bilateral", "shortest_name_length": 36}
{"curie": "MONDO:0004959", "names": ["Plasma Cell Tumor", "Plasmacytic Tumor", "Plasmacytic tumor", "Plasma cell tumor", "plasmacytic tumor", "plasma cell tumor", "Plasma cell tumour", "plasmacytic tumour", "Plasmacytic Tumour", "plasma cell tumour", "Plasma Cell Tumors", "Plasma Cell Neoplasm", "Plasma cell neoplasm", "plasma cell disorder", "Plasmacytic Neoplasm", "plasma cell neoplasm", "Plasma cell disorder", "plasmacytic neoplasm", "Plasma Cell Neoplasms", "Plasma cell dyscrasia", "cell dyscrasia plasma", "Plasma cell neoplasms", "Neoplasm, Plasma Cell", "plasma cell dyscrasia", "Plasma Cell Dyscrasia", "cell disorders plasma", "Dyscrasia, Plasma Cell", "cell dyscrasias plasma", "Neoplasms, Plasma Cell", "Cell Dyscrasia, Plasma", "plasma cell dyscrasias", "Plasma Cell Dyscrasias", "Plasma cell disorder NOS", "Plasma cell dyscrasia, NOS", "PLASMA CELL TUMOR, MALIGNANT", "plasma cell tumor, malignant", "Plasma cell neoplasm (disorder)", "Plasma cell neoplasm (morphology)", "Plasma cell neoplasm (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "plasma cell neoplasm", "shortest_name_length": 17}
{"curie": "MONDO:0025271", "names": ["Bovine Trypanosomiases", "Bovine Trypanosomiasis", "bovine Trypanosomiases", "bovine trypanosomiasis", "trypanosomiasis, bovine", "Trypanosomiases, bovine", "Trypanosomiases, Bovine", "Trypanosomiasis, Bovine"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trypanosomiasis, bovine", "shortest_name_length": 22}
{"curie": "UMLS:C0265191", "names": ["Secondary Lymphedema", "lymphedema secondary", "Secondary lymphedema", "secondary; lymphedema", "lymphedema; secondary", "Lymphedema, secondary", "Secondary lymphoedema", "Chronic acquired lymphedema", "Chronic acquired lymphoedema", "Secondary lymphedema (diagnosis)", "Chronic acquired lymphedema (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Chronic acquired lymphedema", "shortest_name_length": 20}
{"curie": "UMLS:C4053956", "names": ["Systemic Lupus Erythematosus Nephritis Class IV S"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Systemic Lupus Erythematosus Nephritis Class IV S", "shortest_name_length": 49}
{"curie": "MONDO:0008152", "names": ["MCTO", "Carnevale canun Mendoza syndrome", "multicentric osteolysis nephropathy", "autosomal dominant multicentric osteolysis", "MULTICENTRIC OSTEOLYSIS, AUTOSOMAL DOMINANT", "multicentric osteolysis, autosomal dominant", "Multicentric Osteolysis, Autosomal Dominant", "Multicentric Carpotarsal Osteolysis Syndrome", "Multicentric carpotarsal osteolysis syndrome", "osteolysis multicentric carpotarsal syndrome", "multicentric carpotarsal osteolysis syndrome", "MULTICENTRIC CARPOTARSAL OSTEOLYSIS SYNDROME", "Multicentric carpotarsal osteolysis syndrome (disorder)", "Multicentric carpotarsal osteolysis syndrome (diagnosis)", "Idiopathic multicentric osteolysis with or without nephropathy", "idiopathic multicentric osteolysis with or without nephropathy", "Multicentric carpo-tarsal osteolysis with or without nephropathy", "multicentric carpo-tarsal osteolysis with or without nephropathy", "hereditary osteolysis of carpal bones with or without nephropathy", "OSTEOLYSIS, HEREDITARY, OF CARPAL BONES WITH OR WITHOUT NEPHROPATHY", "Osteolysis, Hereditary, Of Carpal Bones With Or Without Nephropathy", "osteolysis, hereditary, of carpal bones with or without nephropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multicentric carpo-tarsal osteolysis with or without nephropathy", "shortest_name_length": 4}
{"curie": "MONDO:0008357", "names": ["Schmitt-Gillenwater-Kelly syndrome", "Schmitt Gillenwater Kelly syndrome", "radial hypoplasia, triphalangeal thumbs and hypospadias", "Radial hypoplasia, triphalangeal thumbs and hypospadias", "radial hypoplasia triphalangeal thumbs hypospadias maxillary diastema", "Radial hypoplasia triphalangeal thumbs hypospadias maxillary diastema", "radial hypoplasia, triphalangeal thumbs, hypospadias, and maxillary diastema", "RADIAL HYPOPLASIA, TRIPHALANGEAL THUMBS, HYPOSPADIAS, AND MAXILLARY DIASTEMA", "Radial hypoplasia, triphalangeal thumbs, hypospadias, and maxillary diastema", "radial hypoplasia-triphalangeal thumbs-hypospadias-maxillary diastema syndrome", "Radial hypoplasia-triphalangeal thumbs-hypospadias-maxillary diastema syndrome", "Radial hypoplasia and triphalangeal thumb with hypospadias and maxillary diastema syndrome", "Radial hypoplasia and triphalangeal thumb with hypospadias and maxillary diastema syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "radial hypoplasia-triphalangeal thumbs-hypospadias-maxillary diastema syndrome", "shortest_name_length": 34}
{"curie": "MONDO:0012154", "names": ["MYP6", "MYOPIA 6", "Myopia 6", "myopia 6", "myopia type 6", "MYOPIA 6 (disorder)", "SCO2 myopia (disease)", "myopia, susceptibility to", "myopia (disease) caused by mutation in SCO2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopia 6", "shortest_name_length": 4}
{"curie": "MONDO:0035547", "names": ["predisposition to severe viral infection due to IRF7 deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "predisposition to severe viral infection due to IRF7 deficiency", "shortest_name_length": 63}
{"curie": "MONDO:0011322", "names": ["Oroacral syndrome, Verloes-Koulischer type", "Oroacral Syndrome, Verloes-Koulischer Type", "OROACRAL SYNDROME, VERLOES-KOULISCHER TYPE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Oroacral syndrome, Verloes-Koulischer type", "shortest_name_length": 42}
{"curie": "MONDO:0008001", "names": ["MEM", "Multiple eruptive milia", "milia, multiple eruptive", "Milia, Multiple Eruptive", "MILIA, MULTIPLE ERUPTIVE", "Multiple eruptive milia (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "milia, multiple eruptive", "shortest_name_length": 3}
{"curie": "MONDO:0005050", "names": ["invasive duct and lobular carcinoma", "Invasive Duct and Lobular Carcinoma", "Invasive Ductal and Lobular Carcinoma", "invasive ductal and lobular carcinoma", "Infiltrating duct and lobular carcinoma", "Infiltrating Ductal and Lobular Carcinoma", "infiltrating ductal and lobular carcinoma", "invasive breast ductal and lobular carcinoma", "Infiltrating duct mixed with other types of carcinoma", "Invasive Breast Ductal Carcinoma and Lobular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "invasive ductal and lobular carcinoma", "shortest_name_length": 35}
{"curie": "UMLS:C4725861", "names": ["Visceral Metastases", "Secondary malignant neoplasm of viscera", "Metastatic malignant neoplasm of viscus", "Secondary Malignant Neoplasm of Viscera", "malignant neoplasm of viscera secondary", "Metastatic malignant neoplasm to viscera", "Metastatic malignant neoplasm of viscera", "Metastatic Malignant Neoplasm in the Viscera", "Metastatic malignant neoplasm to viscera (disorder)", "Secondary malignant neoplasm of viscera (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic malignant neoplasm to viscera", "shortest_name_length": 19}
{"curie": "MONDO:0009843", "names": ["HLD3", "AIMP1 leukodystrophy", "hypomyelinating leukodystrophy 3", "leukodystrophy, hypomyelinating 3", "LEUKODYSTROPHY, HYPOMYELINATING, 3", "leukodystrophy, hypomyelinating, 3", "Leukodystrophy, Hypomyelinating, 3", "perinatal Sudanophilic leukodystrophy", "Perinatal Sudanophilic leukodystrophy", "hypomyelinating leukodystrophy type 3", "leukodystrophy, hypomyelinating, type 3", "leukodystrophy caused by mutation in AIMP1", "Pelizaeus-Merzbacher-like disease due to AIMP1 mutation", "Pelizaeus-Merzbacher-like disease, autosomal recessive, 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "hypomyelinating leukodystrophy 3", "shortest_name_length": 4}
{"curie": "MONDO:0008878", "names": ["bone dysplasia lethal Holmgren type", "Bone dysplasia lethal Holmgren type", "bone dysplasia, lethal Holmgren type", "Bone dysplasia, lethal Holmgren type", "Bone Dysplasia, Lethal, Holmgren Type", "BONE DYSPLASIA, LETHAL, HOLMGREN TYPE", "bone dysplasia, lethal, Holmgren type", "Bone dysplasia lethal Holmgren type (disorder)", "Autosomal recessive lethal chondrodysplasia round femoral inferior epiphysis type", "Autosomal recessive lethal chondrodysplasia, round femoral inferior epiphysis type", "autosomal recessive lethal chondrodysplasia, round femoral inferior epiphysis type"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bone dysplasia, lethal Holmgren type", "shortest_name_length": 35}
{"curie": "MONDO:0023214", "names": ["gas bloat syndrome", "Gas bloat syndrome", "Post-fundoplication syndrome", "post-fundoplication syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gas bloat syndrome", "shortest_name_length": 18}
{"curie": "MONDO:0010752", "names": ["VACTERLX", "VACTERL-H, X-LINKED", "VACTERL-H, X-linked", "X-linked VACTERL-H syndrome", "X-linked VACTERL association", "VACTERL association with hydrocephaly, X-linked", "VACTERL association, X-linked, X-linked recessive", "VACTERL association, X-linked with or without hydrocephalus", "VACTERL association, X-linked, with or without hydrocephalus", "VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "VACTERL association, X-linked, with or without hydrocephalus", "shortest_name_length": 8}
{"curie": "UMLS:C2711653", "names": ["Epilepsy characterized by intractable complex partial seizures", "Epilepsy characterised by intractable complex partial seizures", "Epilepsy characterized by intractable complex partial seizures (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epilepsy characterized by intractable complex partial seizures", "shortest_name_length": 62}
{"curie": "UMLS:C0338434", "names": ["Cerebral actinomycoma", "Actinomycotic brain abscess", "Actinomycotic Cerebral Abscess", "Actinomycotic brain abscess (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Actinomycotic brain abscess", "shortest_name_length": 21}
{"curie": "MONDO:0013625", "names": ["PARK17", "PARKINSON DISEASE 17", "Parkinson disease 17", "Parkinson's disease 17", "VPS35 Parkinson disease", "Parkinson disease type 17", "autosomal dominant Parkinson disease 17", "Parkinson disease caused by mutation in VPS35"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Parkinson disease 17", "shortest_name_length": 6}
{"curie": "MONDO:0024868", "names": ["Metastatic Carcinoma to the Adrenal Medulla", "metastatic carcinoma in the adrenal medulla", "metastatic carcinoma to the adrenal medulla", "Metastatic Carcinoma in the Adrenal Medulla"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "metastatic carcinoma in the adrenal medulla", "shortest_name_length": 43}
{"curie": "MONDO:0010597", "names": ["ADP-ribose Protein hydrolase deficiency", "ADP-RIBOSE PROTEIN HYDROLASE DEFICIENCY", "ADP-Ribose Protein Hydrolase Deficiency", "glutamyl ribose-5-phosphate storage disease", "Glutamyl Ribose-5-Phosphate Storage Disease", "GLUTAMYL RIBOSE-5-PHOSPHATE STORAGE DISEASE"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "glutamyl ribose-5-phosphate storage disease", "shortest_name_length": 39}
{"curie": "MONDO:0012225", "names": ["SLSN5", "SENIOR-Loken syndrome 5", "SENIOR-LOKEN SYNDROME 5", "Senior-Loken Syndrome 5", "Senior-Loken syndrome 5", "IQCB1 Senior-Loken syndrome", "Senior-Loken syndrome type 5", "Senior-Loken syndrome caused by mutation in IQCB1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Senior-Loken syndrome 5", "shortest_name_length": 5}
{"curie": "MONDO:0013409", "names": ["ARMD5", "age related macular degeneration 5", "macular degeneration, age-related, 5", "MACULAR DEGENERATION, AGE-RELATED, 5", "ERCC6 age-related macular degeneration", "age related macular degeneration type 5", "macular Degeneration, age-related, type 5", "macular degeneration, age-related, susceptibility to, 5", "age-related macular degeneration caused by mutation in ERCC6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "age related macular degeneration 5", "shortest_name_length": 5}
{"curie": "MONDO:0043120", "names": ["Male pseudohermaphroditism due to defective LH molecule", "male pseudohermaphroditism due to defective lh molecule"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "male pseudohermaphroditism due to defective lh molecule", "shortest_name_length": 55}
{"curie": "UMLS:C2828018", "names": ["Stage IV Merkel Cell Cancer", "Stage IV Merkel Cell Carcinoma", "stage IV Merkel cell carcinoma", "Stage IV Merkel Cell Carcinoma AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IV Merkel Cell Carcinoma AJCC v7", "shortest_name_length": 27}
{"curie": "UMLS:C0347534", "names": ["Meninges Cyst", "meningeal cyst", "Meningeal Cyst", "Meningeal cyst", "cysts meningeal", "Cyst of Meninges", "Cyst of the Meninges", "Meningeal cyst (disorder)", "meningeal cyst (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Meningeal cyst", "shortest_name_length": 13}
{"curie": "MONDO:0004349", "names": ["retina lymphoma", "retinal lymphoma", "Retinal Lymphoma", "Lymphoma of Retina", "Lymphoma of retina", "lymphoma of retina", "Lymphoma of the Retina", "lymphoma of the retina", "primary retinal lymphoma", "Primary Retinal Lymphoma", "Lymphoma of retina (disorder)", "lymphoma of retina (diagnosis)", "Primary Retinal Non-Hodgkin Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "retina lymphoma", "shortest_name_length": 15}
{"curie": "MONDO:0033375", "names": ["OFD17", "Ofds 17", "OFDS XVII", "orofaciodigital syndrome 17", "OROFACIODIGITAL SYNDROME XVII", "orofaciodigital syndrome XVII", "oral-Facial-digital syndrome, type 17", "ORAL-FACIAL-DIGITAL SYNDROME, TYPE XVII"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "orofaciodigital syndrome 17", "shortest_name_length": 5}
{"curie": "MONDO:0006678", "names": ["cystolith", "Cystolith", "Cystoliths", "Stone;bladder", "bladder stone", "Bladder Stone", "Bladder stone", "stones bladder", "Stone, Bladder", "Bladder stones", "Bladder Stones", "bladder stones", "Bladder Calculi", "vesicolithiasis", "Vesicolithiasis", "Vesical Calculi", "bladder calculi", "vesical calculi", "Stones, Bladder", "bladder calculus", "Calculi, Bladder", "Bladder--Calculi", "Calculus;bladder", "vesical calculus", "Bladder calculus", "BLADDER CALCULUS", "Vesical Calculus", "Vesical calculus", "Bladder Calculus", "Calculi, Vesical", "Calculus bladder", "BLADDER, CALCULUS", "bladder; calculus", "calculus; bladder", "Calculus, Bladder", "Calculus, Vesical", "Calculus in bladder", "Calculus of bladder", "Stone urinary bladder", "Urinary Bladder Stone", "Urinary bladder stone", "urinary bladder stone", "bladder stones urinary", "Urinary Bladder Stones", "Stone, Urinary Bladder", "Bladder Stone, Urinary", "Stones, Urinary Bladder", "Urinary Bladder Calculi", "Bladder Stones, Urinary", "Urolithiasis of bladder", "Calculi, Urinary Bladder", "Urinary Bladder Calculus", "Bladder Calculi, Urinary", "Calculus urinary bladder", "CALCULUS URINARY BLADDER", "Calculus, Urinary Bladder", "Bladder Calculus, Urinary", "Calculi of Urinary Bladder", "bladder calculus (diagnosis)", "Urinary bladder stone (disorder)", "Urinary Bladder Calculi (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder calculus", "shortest_name_length": 9}
{"curie": "UMLS:C0376416", "names": ["Myocardial Hibernation", "Hibernation, Myocardial"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hibernation, Myocardial", "shortest_name_length": 22}
{"curie": "MONDO:0011919", "names": ["AIS1", "VAMAS2", "FOXD3 autoimmune disease", "susceptibility to autoimmune disease 1", "autoimmune disease, susceptibility to, 1", "AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 1", "autoimmune disease, susceptibility to, type 1", "autoimmune disease caused by mutation in FOXD3", "autoimmune disease susceptibility locus, chromosome 1P-related", "AUTOIMMUNE DISEASE SUSCEPTIBILITY LOCUS, CHROMOSOME 1p-RELATED", "vitiligo-associated multiple autoimmune disease susceptibility 2", "VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autoimmune disease, susceptibility to, 1", "shortest_name_length": 4}
{"curie": "UMLS:C0276500", "names": ["HIV I infection", "HIV I infection (diagnosis)", "Human immunodeficiency virus 1 infection", "Human immunodeficiency virus I infection", "Human immunodeficiency virus I infection (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Human immunodeficiency virus I infection", "shortest_name_length": 15}
{"curie": "UMLS:C4288040", "names": ["Vaginal Germ Cell Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Vaginal Germ Cell Tumor", "shortest_name_length": 23}
{"curie": "UMLS:C5420043", "names": ["Sinonasal Soft Tissue Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sinonasal Soft Tissue Neoplasm", "shortest_name_length": 30}
{"curie": "MONDO:0030862", "names": ["COACH3", "COACH SYNDROME 3", "COACH syndrome 3"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "COACH syndrome 3", "shortest_name_length": 6}
{"curie": "MONDO:0044689", "names": ["RINR", "recurrent idiopathic neuroretinitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "recurrent idiopathic neuroretinitis", "shortest_name_length": 4}
{"curie": "UMLS:C4725917", "names": ["Methotrexate-Associated Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Methotrexate-Associated Lymphoma", "shortest_name_length": 32}
{"curie": "UMLS:C0848377", "names": ["wound; abdomen", "abdomen injury", "abdomen trauma", "injury abdomen", "trauma abdomen", "Trauma;abdomen", "abdomen; wound", "injury; abdomen", "abdomen; injury", "Abdominal trauma", "abdominal trauma", "abdominal injury", "Abdominal Injury", "Abdominal injury", "abdomen injuries", "Injury, Abdominal", "Injury of abdomen", "Abdominal Injuries", "abdominal injuries", "Injuries, Abdominal", "Abdominal injury NOS", "trauma to the abdomen", "abdomen injury (diagnosis)", "Injury of abdomen (disorder)", "abdominal trauma (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trauma to the abdomen", "shortest_name_length": 14}
{"curie": "UMLS:C0919532", "names": ["Genome Instability", "genome instability", "genomes instability", "Genomic Instability", "Instability, Genome", "Genome Instabilities", "Instability, Genomic", "Genomic Instabilities", "Instabilities, Genome", "Instabilities, Genomic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Genomic Instability", "shortest_name_length": 18}
{"curie": "MONDO:0011119", "names": ["IGDS", "IRID", "IRID 1", "IRID 2", "iridogoniodysgenesis", "iridogoniodysgenesis type 1", "iridogoniodysgenesis type 2", "iridogoniodysgenesis syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "iridogoniodysgenesis", "shortest_name_length": 4}
{"curie": "MONDO:0004394", "names": ["Maxillary Sinus Epidermoid Carcinoma", "maxillary sinus epidermoid carcinoma", "maxillary antrum epidermoid carcinoma", "Epidermoid Carcinoma of Maxillary Sinus", "Maxillary Sinus Squamous Cell Carcinoma", "maxillary sinus squamous cell carcinoma", "epidermoid carcinoma of maxillary sinus", "epidermoid carcinoma of maxillary antrum", "maxillofacial sinus epidermoid carcinoma", "maxillary antrum squamous cell carcinoma", "Squamous Cell Carcinoma of Maxillary Sinus", "squamous cell carcinoma of maxillary sinus", "Squamous cell carcinoma of maxillary sinus", "epidermoid carcinoma of the maxillary sinus", "epidermoid carcinoma of maxillofacial sinus", "maxillofacial sinus squamous cell carcinoma", "Epidermoid Carcinoma of the Maxillary Sinus", "squamous cell carcinoma of maxillary antrum", "epidermoid carcinoma of the maxillary antrum", "squamous cell carcinoma of the maxillary sinus", "Squamous Cell Carcinoma of the Maxillary Sinus", "squamous cell carcinoma of maxillofacial sinus", "epidermoid carcinoma of the maxillofacial sinus", "Epidermoid carcinoma of the Maxillofacial sinus", "squamous cell carcinoma of the maxillary antrum", "Primary squamous cell carcinoma of maxillary sinus", "squamous cell carcinoma of the maxillofacial sinus", "Squamous cell carcinoma of maxillary sinus (disorder)", "Squamous cell carcinoma of maxillary sinus (diagnosis)", "Primary squamous cell carcinoma of maxillary sinus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "maxillary sinus squamous cell carcinoma", "shortest_name_length": 36}
{"curie": "UMLS:C1335166", "names": ["Ovarian Mixed Germ Cell-Sex Cord Tumor", "Ovarian Germ Cell-Sex Cord-Stromal Tumor", "Ovarian Mixed Germ Cell-Sex Cord Neoplasm", "Ovarian Mixed Germ Cell-Sex Cord-Stromal Tumor", "Ovarian Mixed Germ Cell-Sex Cord-Stromal Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Ovarian Mixed Germ Cell-Sex Cord-Stromal Tumor", "shortest_name_length": 38}
{"curie": "MONDO:0016258", "names": ["Uterine Corpus Carcinofibroma", "uterine corpus carcinofibroma", "uterine corpus Carcinofibroma", "Carcinofibroma of the corpus uteri"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "uterine corpus carcinofibroma", "shortest_name_length": 29}
{"curie": "MONDO:0007876", "names": ["Labd", "LABD", "Plott syndrome", "PLOTT SYNDROME", "GERHARDT SYNDROME", "Gerhardt syndrome", "Laryngeal abductor paralysis", "LARYNGEAL ABDUCTOR PARALYSIS", "laryngeal abductor paralysis", "Familial vocal cord dysfunction", "familial vocal cord dysfunction", "vocal cord dysfunction familial", "Vocal cord dysfunction familial", "Vocal Cord Dysfunction, Familial", "vocal cord dysfunction, familial", "VOCAL CORD DYSFUNCTION, FAMILIAL", "Congenital laryngeal abductor palsy", "Congenital laryngeal abductor paralysis", "hereditary abductor vocal cord paralysis", "Congenital laryngeal abductor palsy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laryngeal abductor paralysis", "shortest_name_length": 4}
{"curie": "UMLS:C0279624", "names": ["adult acute M2 leukemia", "Adult Acute M2 Leukemia", "M2 leukemia, adult acute", "M2 Adult Acute Myeloid Leukemia", "M2 Adult Acute Myelocytic Leukemia", "M2 Adult Acute Myelogenous Leukemia", "M2 Adult Acute Granulocytic Leukemia", "M2 Adult Acute Myeloblastic Leukemia", "Acute Myeloid Leukemia (AML) with Maturation", "Adult Acute Myeloid Leukemia with Maturation", "Adult Acute Myelocytic Leukemia with Maturation", "M2 Adult Acute Myeloid Leukemia with Maturation", "Adult Acute Myelogenous Leukemia with Maturation", "Adult Acute Granulocytic Leukemia with Maturation", "Adult Acute Myeloblastic Leukemia with Maturation", "M2 Adult Acute Myelocytic Leukemia with Maturation", "M2 Adult Acute Myelogenous Leukemia with Maturation", "M2 adult acute myeloblastic leukemia with maturation", "M2 Adult Acute Granulocytic Leukemia with Maturation", "M2 Adult Acute Myeloblastic Leukemia with Maturation", "Adult Acute Myeloblastic Leukemia with Maturation (M2)", "adult acute myeloblastic leukemia with maturation (M2)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Acute Myeloid Leukemia with Maturation", "shortest_name_length": 23}
{"curie": "MONDO:0041095", "names": ["Pseudomonas aeruginosa malignant otitis externa", "malignant otitis externa due to Pseudomonas aeruginosa", "Pseudomonas aeruginosa caused malignant otitis externa", "Malignant otitis externa due to Pseudomonas aeruginosa", "malignant otitis externa caused by Pseudomonas aeruginosa", "Malignant otitis externa caused by Pseudomonas aeruginosa", "Malignant otitis externa caused by Pseudomonas aeruginosa (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malignant otitis externa caused by Pseudomonas aeruginosa", "shortest_name_length": 47}
{"curie": "MONDO:0010429", "names": ["MRX96", "XLID96", "X-linked mental retardation 96", "mental retardation, X-linked 96", "MENTAL RETARDATION, X-LINKED 96", "mental retardation, X-linked type 96", "intellectual disability, X-linked 96", "intellectual disability, X-linked type 96", "INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 96", "non-syndromic X-linked intellectual disability 96", "SYP non-syndromic X-linked intellectual disability", "intellectual developmental disorder, X-linked 96, X-linked recessive", "non-syndromic X-linked intellectual disability caused by mutation in SYP"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intellectual disability, X-linked 96", "shortest_name_length": 5}
{"curie": "MONDO:0001775", "names": ["chronic duodenal ileus", "Chronic duodenal ileus", "Duodenal ileus (chronic)", "Chronic duodenal ileus (disorder)", "chronic duodenal ileus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chronic duodenal ileus", "shortest_name_length": 22}
{"curie": "UMLS:C1336008", "names": ["Small Intestinal Small Cell Carcinoma", "Small Intestinal Small Cell Neuroendocrine Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Small Intestinal Small Cell Neuroendocrine Carcinoma", "shortest_name_length": 37}
{"curie": "MONDO:0013216", "names": ["DBA9", "DIAMOND-BLACKFAN ANEMIA 9", "Diamond-Blackfan anemia 9", "Diamond-Blackfan Anemia 9", "RPS10 Diamond-Blackfan anemia", "Diamond-Blackfan Anemia type 9", "RPS10-related Diamond-Blackfan anemia", "Diamond-Blackfan anemia caused by mutation in RPS10"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Diamond-Blackfan anemia 9", "shortest_name_length": 4}
{"curie": "MONDO:0010144", "names": ["THM", "Thm", "agenesis; tibia", "tibia; agenesis", "Tibial agenesis", "Absence of Tibia", "absence of tibia", "Tibial hemimelia", "TIBIAL HEMIMELIA", "Absence of tibia", "tibial hemimelia", "Agenesis of tibia", "tibia, absence of", "Tibia, absence of", "TIBIA, ABSENCE OF", "agenesis of tibia", "Absence of tibia (finding)", "Congenital absence of tibia", "congenital absence of tibia", "Agenesis of tibia (disorder)", "Tibial longitudinal meromelia", "tibial longitudinal meromelia", "agenesis of tibia (diagnosis)", "Bilateral absence of the tibia", "bilateral absence of the tibia", "Congenital absence of tibia (disorder)", "congenital longitudinal deficiency of the tibia", "Congenital longitudinal deficiency of the tibia", "congenital aplasia and dysplasia of the tibia with intact fibula", "Congenital aplasia and dysplasia of the tibia with intact fibula", "Congenital absence of tibia with or without absence of some distal elements", "Congenital absence of tibia with or without absence of some, but not all, distal elements"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tibial hemimelia", "shortest_name_length": 3}
{"curie": "MONDO:0013831", "names": ["KTCN6", "KERATOCONUS 6", "keratoconus 6"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratoconus 6", "shortest_name_length": 5}
{"curie": "UMLS:C0854260", "names": ["Congenital urinary tract obstruction", "Congenital Urinary Tract Obstruction"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Congenital urinary tract obstruction", "shortest_name_length": 36}
{"curie": "MONDO:0011858", "names": ["SPAR", "Spar", "SPASTIC PARAPLEGIA, ATAXIA, AND MENTAL RETARDATION", "Spastic Paraplegia, Ataxia, And Mental Retardation", "spastic paraplegia, ataxia, and mental retardation", "spastic paraplegia, ataxia, and intellectual disability", "SPASTIC PARAPLEGIA, ATAXIA, AND INTELLECTUAL DEVELOPMENTAL DISORDER"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spastic paraplegia, ataxia, and intellectual disability", "shortest_name_length": 4}
{"curie": "UMLS:C0342382", "names": ["Growth Hormone Neurosecretory Dysfunction", "Growth hormone neurosecretory dysfunction", "Growth hormone neurosecretory dysfunction (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Growth hormone neurosecretory dysfunction", "shortest_name_length": 41}
{"curie": "UMLS:C0349785", "names": ["Psychogenic torticollis", "torticollis psychogenic", "Psychogenic Torticollis", "psychogenic torticollis", "Torticollis psychogenic", "Torticollis, Psychogenic", "Psychosomatic torticollis", "Psychogenic torticollis (disorder)", "Psychogenic torticollis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Torticollis, Psychogenic", "shortest_name_length": 23}
{"curie": "UMLS:C4527423", "names": ["Refractory Abdominal Neuroendocrine Tumor", "Refractory Abdominal Neuroendocrine Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Refractory Abdominal Neuroendocrine Neoplasm", "shortest_name_length": 41}
{"curie": "UMLS:C5243614", "names": ["Anticoagulant-related nephropathy"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Anticoagulant-related nephropathy", "shortest_name_length": 33}
{"curie": "MONDO:0002420", "names": ["Tic", "tic", "TIC", "tics", "Tics", "TICS", "Tic NOS", "Tic, NOS", "Spasm/Tic", "Habit tic", "tic; spasm", "habit; tic", "tic; habit", "spasm; tic", "Habit spasm", "habit spasm", "Habit Spasm", "Tic Disorder", "Spasm, Habit", "tic disorder", "Habit Spasms", "TIC DISORDER", "Tic disorder", "spasm; habit", "habit; spasm", "Habit Chorea", "tic disorders", "TIC DISORDERS", "habit; chorea", "Tic Disorders", "habitual; tic", "Chorea, Habit", "Tic (finding)", "Tic disorders", "tic; habitual", "chorea; habit", "Spasms, Habit", "Habit Choreas", "habit disorder", "tics were seen", "behavioral tic", "Behavioral tic", "Habit disorder", "Choreas, Habit", "Behavioural tic", "disorder; habit", "disorders habit", "habitual; spasm", "Tic, behavioral", "spasm; habitual", "tic disorder nos", "Tic disorder NOS", "Habituation Spasm", "Tic disorder, NOS", "Spasm, Habituation", "Habituation Spasms", "habit tic disorder", "Spasms, Habituation", "Habit tic (disorder)", "tics (physical finding)", "Tic disorder (disorder)", "Unspecified tic disorder", "tic disorder (diagnosis)", "Tic disorder, unspecified", "habit tic disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "tic disorder", "shortest_name_length": 3}
{"curie": "MONDO:0007147", "names": ["OSA", "Osa", "OSAS", "SAHS", "OSAHS", "Obstructive apnea", "Obstructive Apnea", "Apnea, obstructive", "Obstructive Sleep Apnea", "obstructive sleep apnea", "apnea obstructive sleep", "Obstructive sleep apnea", "Apnea, Obstructive Sleep", "APNEA, OBSTRUCTIVE SLEEP", "Obstructive sleep apnoea", "apnea, obstructive sleep", "obstructive sleep apnoea", "Sleep apnea, obstructive", "Sleep Apnea, Obstructive", "obstructive sleep Apneas", "Obstructive Sleep Apneas", "Apneas, obstructive sleep", "Sleep Apneas, Obstructive", "sleep Apneas, obstructive", "Apneas, Obstructive Sleep", "apnea obstructive sleeping", "obstructive sleep osa apnea", "OSA - Obstructive sleep apnea", "SLEEP APNEA/HYPOPNEA SYNDROME", "sleep apnea/hypopnea syndrome", "Sleep Apnea Hypopnea Syndrome", "sleep apnea hypopnea syndrome", "Sleep apnea-hypopnea syndrome", "OSA - Obstructive sleep apnoea", "Sleep apnoea-hypopnoea syndrome", "obstructive sleep apnea syndrome", "OBSTRUCTIVE SLEEP APNEA SYNDROME", "sleep apnea obstructive syndrome", "Obstructive sleep apnea syndrome", "Obstructive Sleep Apnea Syndrome", "Syndrome, Obstructive Sleep Apnea", "syndrome, obstructive sleep apnea", "Obstructive sleep apnoea syndrome", "sleep apnea syndrome, obstructive", "Sleep Apnea Syndrome, Obstructive", "Syndrome, Sleep Apnea, Obstructive", "syndrome, sleep apnea, obstructive", "obstructive sleep apnea (diagnosis)", "Obstructive sleep apnea (adult)(pediatric)", "Obstructive sleep apnea (adult) (pediatric)", "Obstructive sleep apnea syndrome (disorder)", "upper airway resistance sleep apnea syndrome", "syndrome, upper airway resistance, sleep apnea"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "obstructive sleep apnea syndrome", "shortest_name_length": 3}
{"curie": "MONDO:0001204", "names": ["esophagus sarcoma", "Esophagus Sarcoma", "Esophageal Sarcoma", "esophageal sarcoma", "sarcoma, esophagus", "Sarcoma, Esophagus", "Sarcoma of Esophagus", "sarcoma of esophagus", "Sarcoma of the Esophagus", "sarcoma of the esophagus", "sarcoma of esophagus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "esophagus sarcoma", "shortest_name_length": 17}
{"curie": "UMLS:C0334613", "names": ["Pigmented Neurofibroma", "Pigmented neurofibroma", "Melanotic Neurofibroma", "Melanotic neurofibroma", "Melanotic neurofibroma (morphologic abnormality)", "Pigmented neurofibroma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Melanotic neurofibroma", "shortest_name_length": 22}
{"curie": "MONDO:0013795", "names": ["FBCG2", "FIBROCHONDROGENESIS 2", "fibrochondrogenesis 2", "fibrochondrogenesis type 2", "COL11A2 fibrochondrogenesis", "fibrochondrogenesis caused by mutation in COL11A2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fibrochondrogenesis 2", "shortest_name_length": 5}
{"curie": "MONDO:0033619", "names": ["MEPCA", "myopathy, epilepsy, and progressive cerebral atrophy", "MYOPATHY, EPILEPSY, AND PROGRESSIVE CEREBRAL ATROPHY"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopathy, epilepsy, and progressive cerebral atrophy", "shortest_name_length": 5}
{"curie": "EFO:1001504", "names": ["small vessel stroke"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "small vessel stroke", "shortest_name_length": 19}
{"curie": "UMLS:C0854385", "names": ["Violence-related symptom"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Violence-related symptom", "shortest_name_length": 24}
{"curie": "UMLS:C1336056", "names": ["Spindle Cell Type GIST", "Spindle Cell Type Gastrointestinal Stromal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Spindle Cell Type Gastrointestinal Stromal Tumor", "shortest_name_length": 22}
{"curie": "MONDO:0011539", "names": ["ANM", "NEM5", "NEMALINE MYOPATHY 5", "nemaline myopathy 5", "Nemaline myopathy 5", "nemaline myopathy 5A", "Amish nemaline myopathy", "Amish Nemaline Myopathy", "AMISH NEMALINE MYOPATHY", "TNNT1 nemaline myopathy", "nemaline myopathy type 5", "NEMALINE MYOPATHY, AMISH TYPE", "Nemaline Myopathy, Amish Type", "nemaline myopathy, Amish type", "nemaline myopathy 5, Amish type", "Amish nemaline myopathy (disorder)", "nemaline myopathy caused by mutation in TNNT1", "Nemaline myopathy, caused by mutation in the troponin t1 gene", "nemaline myopathy, caused by mutation in the troponin t1 gene"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "nemaline myopathy 5", "shortest_name_length": 3}
{"curie": "MONDO:0020644", "names": ["Lung Non-Hodgkin Lymphoma", "lung non-Hodgkin lymphoma", "Lung Non-Hodgkin's Lymphoma", "lung non-Hodgkin's lymphoma", "Non-Hodgkin lymphoma of lung", "non-Hodgkin lymphoma of lung", "Non-Hodgkin's lymphoma of lung", "non-Hodgkin's lymphoma of lung", "non hodgkins lymphoma pulmonary", "primary lung non-Hodgkin's lymphoma", "Primary Lung Non-Hodgkin's Lymphoma", "non hodgkins lymphoma involving lung", "Non-Hodgkin's lymphoma of lung (disorder)", "non-Hodgkin's lymphoma of lung (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung non-Hodgkin lymphoma", "shortest_name_length": 25}
{"curie": "UMLS:C1514949", "names": ["Stage I Centroblastic Follicular Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage I Centroblastic Follicular Lymphoma", "shortest_name_length": 41}
{"curie": "MONDO:0020598", "names": ["MALABSORPTION", "malabsorption", "Malabsorption", "Malabsorption, NOS", "malabsorption syndrome", "Syndrome malabsorption", "Malabsorption Syndrome", "SYNDROME MALABSORPTION", "MALABSORPTION SYNDROME", "Malabsorption syndrome", "Syndrome, Malabsorption", "malabsorption; syndrome", "syndrome; malabsorption", "Malabsorption Syndromes", "Malabsorption syndromes", "malabsorption syndromes", "MALABSORPTION SYNDROMES", "intestinal malabsorption", "Intestinal malabsorption", "Syndromes, Malabsorption", "intestinal; malabsorption", "malabsorption; intestinal", "Malabsorption syndrome NOS", "Malabsorption syndrome, NOS", "Intestinal malabsorption, NOS", "Malabsorption syndrome (disorder)", "malabsorption syndrome (diagnosis)", "MALNUTRITION MALABSORPTION SYNDROME", "Intestinal malabsorption (disorder)", "gastrointestinal absorption disorder", "Unspecified intestinal malabsorption", "Intestinal malabsorption, unspecified"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "malabsorption syndrome", "shortest_name_length": 13}
{"curie": "UMLS:C1261283", "names": ["Actinomycetoma", "actinomycetoma", "Actinomycetomas", "Actinomycotic mycetoma", "Actinomycotic mycetema", "mycetoma; actinomycotic", "actinomycosis; mycetoma", "actinomycotic; mycetoma", "mycetoma; actinomycosis", "Actinomycotic madura foot", "Actinomycetoma (diagnosis)", "Madura foot - actinomycotic", "Actinomycotic maduromycosis", "Actinomycotic schizomycetoma", "foot; mycetoma, actinomycotic", "mycetoma; foot, actinomycotic", "Actinomycotic mycetoma of foot", "Actinomycotic mycetoma (disorder)", "mycetoma; infection, actinomycotic", "infection; mycetoma, actinomycotic", "Madura foot due to Actinomadura, NOS", "Madura foot - actinomycotic (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Actinomycetoma", "shortest_name_length": 14}
{"curie": "UMLS:C4524747", "names": ["Postneoadjuvant Therapy Stage IIIA Gastroesophageal Junction Adenocarcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Postneoadjuvant Therapy Stage IIIA Gastroesophageal Junction Adenocarcinoma AJCC v8", "shortest_name_length": 83}
{"curie": "MONDO:0030923", "names": ["frontotemporal dementia and/or amyotrophic lateral sclerosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "frontotemporal dementia and/or amyotrophic lateral sclerosis", "shortest_name_length": 60}
{"curie": "MONDO:0004186", "names": ["cranial nodular fasciitis", "Cranial Nodular Fasciitis", "Cranial Pseudosarcomatous Fasciitis", "cranial pseudosarcomatous fasciitis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cranial nodular fasciitis", "shortest_name_length": 25}
{"curie": "MONDO:0011962", "names": ["endometrial Ca", "endometrium cancer", "Endometrial cancer", "endometrial cancer", "Endometrial Cancer", "endometrial neoplasm", "tumor of endometrium", "tumor of Endometrium", "Cancer of endometrium", "cancer of endometrium", "neoplasm of endometrium", "cancer of the endometrium", "Neoplasm malig;endometrial", "malignant endometrial neoplasm", "Malignant Endometrial Neoplasm", "malignant endometrium neoplasm", "ENDOMETRIAL NEOPLASM MALIGNANT", "Endometrial neoplasm malignant", "endometrial carcinoma, somatic", "Endometrial neoplasms malignant", "malignant neoplasm of endometrium", "Malignant neoplasm of endometrium", "malignant neoplasm of the endometrium", "primary malignant neoplasm of endometrium", "malignant neoplasm of endometrium (diagnosis)", "uterine neoplasm, malignant - of the endometrium", "Malignant neoplasm of endometrium of corpus uteri", "Malignant neoplasm of endometrium of corpus uteri (disorder)", "endometrial cancer, familial, autosomal dominant, somatic mutation", "endometrial cancer, susceptibility to, autosomal dominant, somatic mutation"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "endometrial cancer", "shortest_name_length": 14}
{"curie": "MONDO:0013290", "names": ["AGM5", "agammaglobulinemia 5", "LRRC8A autosomal agammaglobulinemia", "AGAMMAGLOBULINEMIA 5, AUTOSOMAL DOMINANT", "agammaglobulinemia 5, autosomal dominant", "autosomal agammaglobulinemia caused by mutation in LRRC8A", "agammaglobulinemia, autosomal dominant, due to Lrrc8A defect", "AGAMMAGLOBULINEMIA, AUTOSOMAL DOMINANT, DUE TO LRRC8A DEFECT"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "agammaglobulinemia 5, autosomal dominant", "shortest_name_length": 4}
{"curie": "MONDO:0016600", "names": ["classic citrullinemia type 1", "classic citrullinemia type I", "acute neonatal citrullinemia type I", "acute neonatal citrullinemia type 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute neonatal citrullinemia type I", "shortest_name_length": 28}
{"curie": "UMLS:C1708172", "names": ["Gallbladder Clear Cell Adenocarcinoma", "clear cell adenocarcinoma of gallbladder", "clear cell adenocarcinoma of gallbladder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "clear cell adenocarcinoma of gallbladder", "shortest_name_length": 37}
{"curie": "UMLS:C4683746", "names": ["Stage IIIA Mycosis Fungoides and Sezary Syndrome AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Mycosis Fungoides and Sezary Syndrome AJCC v8", "shortest_name_length": 56}
{"curie": "UMLS:C4744556", "names": ["Metastatic Lip and Oral Cavity Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Lip and Oral Cavity Carcinoma", "shortest_name_length": 40}
{"curie": "MONDO:0002627", "names": ["CHOS", "Chondroblastic osteosarcoma", "Chondroblastic Osteosarcoma", "chondroblastic osteosarcoma", "osteosarcoma; chondroblastic", "chondroblastic; osteosarcoma", "osteosarcoma, chondroblastic", "chondrosarcomatous osteosarcoma", "Chondrosarcomatous osteosarcoma", "osteosarcoma, chondrosarcomatous", "Chondroblastic Osteogenic Sarcoma", "chondroblastic osteogenic sarcoma", "osteogenic sarcoma, chondroblastic", "chondrosarcomatous Osteogenic sarcoma", "chondrosarcomatous osteogenic sarcoma", "osteogenic sarcoma, chondrosarcomatous", "sarcoma, osteogenic, chondrosarcomatous", "chondroblastic osteosarcoma (morphologic abnormality)", "Chondroblastic osteosarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chondroblastic osteosarcoma", "shortest_name_length": 4}
{"curie": "UMLS:C0751185", "names": ["headache cough", "Cough Headache", "cough headache", "Headache, Cough", "cough headaches", "coughing headache", "Benign cough headache", "Benign Cough Headache", "Benign Cough Headaches", "Cough Headache, Benign", "Headache, Benign Cough", "Primary Cough Headache", "Primary cough headache", "primary cough headache", "Headache, Primary Cough", "Cough headache syndrome", "Headaches, Benign Cough", "Cough Headaches, Benign", "Valsalva-maneuver Headache", "Cough headache syndrome (finding)", "primary cough headache (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Primary Cough Headache", "shortest_name_length": 14}
{"curie": "MONDO:0015159", "names": ["MCA/MR", "multiple congenital anomalies/dysmorphic syndrome-intellectual disability", "multiple congenital anomalies-intellectual disability with or without dysmorphism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "multiple congenital anomalies/dysmorphic syndrome-intellectual disability", "shortest_name_length": 6}
{"curie": "MONDO:0001307", "names": ["Corneal Abscess", "Corneal abscess", "abscess; cornea", "corneal abscess", "cornea; abscess", "Corneal abscess NOS", "Corneal abscess (disorder)", "corneal abscess (diagnosis)", "corneal abscess (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "corneal abscess", "shortest_name_length": 15}
{"curie": "UMLS:C5238350", "names": ["PALB2-Mutated Breast Carcinoma", "PALB2-Associated Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "PALB2-Associated Breast Carcinoma", "shortest_name_length": 30}
{"curie": "UMLS:C0339962", "names": ["pulmonary mucormycosis", "Pulmonary mucormycosis", "Pulmonary mucormycosis (disorder)", "pulmonary mucormycosis (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pulmonary mucormycosis", "shortest_name_length": 22}
{"curie": "UMLS:C3897749", "names": ["Recurrent Non-Hodgkin Lymphoma", "Recurrent Childhood Non-Hodgkin Lymphoma", "recurrent childhood non-Hodgkin lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Recurrent Childhood Non-Hodgkin Lymphoma", "shortest_name_length": 30}
{"curie": "MONDO:0011547", "names": ["CPP3", "CTPP3", "CTRCT31", "cataract 31 multiple types", "posterior polar cataract 3", "cataract 31, multiple types", "CATARACT 31, MULTIPLE TYPES", "Cataract, posterior polar, 3", "cataract, posterior polar, 3", "CATARACT, POSTERIOR POLAR, 3", "CHMP4B early-onset non-syndromic cataract", "early-onset non-syndromic cataract caused by mutation in CHMP4B"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cataract 31 multiple types", "shortest_name_length": 4}
{"curie": "MONDO:0012522", "names": ["Tndm3", "TNDM3", "diabetes mellitus, transient neonatal 3", "Diabetes mellitus, transient neonatal 3", "DIABETES MELLITUS, TRANSIENT NEONATAL, 3", "diabetes mellitus, transient neonatal, 3", "Diabetes Mellitus, Transient Neonatal, 3", "diabetes mellitus, transient neonatal, type 3", "diabetes mellitus, type II, autosomal dominant", "Diabetes mellitus, transient neonatal 3 (disorder)", "DIABETES MELLITUS, TRANSIENT NEONATAL, 3 (disorder)", "KCNJ11 transient neonatal diabetes mellitus (disease)", "transient neonatal diabetes mellitus (disease) caused by mutation in KCNJ11"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "diabetes mellitus, transient neonatal, 3", "shortest_name_length": 5}
{"curie": "UMLS:C0393068", "names": ["NHL during pregnancy", "non-Hodgkin lymphoma during pregnancy", "Non-Hodgkin Lymphoma During Pregnancy", "pregnancy, non-Hodgkin's lymphoma during"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Non-Hodgkin Lymphoma During Pregnancy", "shortest_name_length": 20}
{"curie": "MONDO:0003331", "names": ["monodermal teratoma", "Monodermal teratoma", "Monodermal Teratoma", "Ovarian Monodermal teratoma", "ovarian monodermal teratoma", "Ovarian Monodermal Teratoma", "monodermal teratoma (morphologic abnormality)", "Monodermal teratoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ovarian monodermal teratoma", "shortest_name_length": 19}
{"curie": "MONDO:0002102", "names": ["CHELITIS", "chelitis", "Cheilitis", "CHEILITIS", "cheilitis", "Cheilitides", "Cheilitis NOS", "Cheilitis, NOS", "lip inflammation", "inflammation lip", "inflammation lips", "Red and sore lips", "Inflammation lips", "inflammation; lip", "lip; inflammation", "Inflammation of lip", "inflammation of lip", "Cheilitis (disorder)", "cheilitis (diagnosis)", "Inflammation of the lips", "inflammation of lip (physical finding)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "cheilitis", "shortest_name_length": 8}
{"curie": "MONDO:0013738", "names": ["DFNB96", "autosomal recessive deafness 96", "DEAFNESS, AUTOSOMAL RECESSIVE 96", "deafness, autosomal recessive 96", "autosomal recessive nonsyndromic deafness 96", "autosomal recessive nonsyndromic hearing loss 96", "autosomal recessive nonsyndromic deafness type 96"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 96", "shortest_name_length": 6}
{"curie": "MONDO:0009691", "names": ["mf", "MF", "MYCOSIS FUNGOIDES", "Mycosis fungoides", "Mycosis Fungoides", "Mycoses fungoides", "mycosis fungoides", "granuloma fungoides", "[M]Mycosis fungoides", "GRANULOMA, FUNGOIDES", "Mycosis fungoides NOS", "MF - Mycosis fungoides", "Alibert-Bazin syndrome", "CTCL/ Mycosis fungoides", "CTCL/ mycosis fungoides", "classic mycosis fungoides", "mycosis fungoides lymphoma", "Mycosis fungoides (disorder)", "Mycosis fungoides (clinical)", "mycosis fungoides (diagnosis)", "Epitheliotropic T-cell lymphoma", "Cutaneous epitheliotropic lymphoma", "Mycosis fungoides, unspecified site", "mycosis fungoides of unspecified site", "mycosis fungoides, Alibert-Bazin type", "mycosis fungoides (morphologic abnormality)", "cutaneous T-cell lymphoma/mycosis fungoides", "Cutaneous T-cell lymphoma/Mycosis fungoides", "Mycosis fungoides (morphologic abnormality)", "mycosis fungoides NOS (morphologic abnormality)", "mycosis fungoides, unspecified site, extranodal and solid organ sites"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mycosis fungoides", "shortest_name_length": 2}
{"curie": "UMLS:C0948149", "names": ["infection spleen", "Splenic Infection", "Splenic infection", "spleen; infection", "infection; spleen", "Infection of spleen", "Splenic infection NOS", "Splenic infection (diagnosis)", "Infection of spleen (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Splenic Infection", "shortest_name_length": 16}
{"curie": "MONDO:0100435", "names": ["SJS1", "SJA syndrome", "Burton syndrome", "Aberfeld syndrome", "Catel-Hempel syndrome", "myotonic chondrodystrophy", "Burton skeletal dysplasia", "Chondrodystrophic myotonia", "Schwartz-Jampel syndrome 1", "osteochondromuscular dystrophy", "Schwartz-Jampel syndrome type 1", "Schwartz Jampel Syndrome, Type 1", "Schwartz-Jampel Syndrome, Type 1", "SCHWARTZ-JAMPEL SYNDROME, TYPE 1", "Schwartz-Jampel syndrome, type 1", "Schwartz-Jampel-Aberfeld syndrome", "Catel-Hempel type dysostosis enchondralis metaepiphysaria", "myotonic myopathy, dwarfism, chondrodystrophy, ocular and facial anomalies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Schwartz-Jampel syndrome type 1", "shortest_name_length": 4}
{"curie": "UMLS:C0014126", "names": ["Endocervical polyp", "ENDOCERVICAL POLYP", "endocervical polyp", "Endocervical Polyp", "endocervical polyps", "Benign endocervical polyp", "Endocervical polyp (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Endocervical polyp", "shortest_name_length": 18}
{"curie": "UMLS:C3273361", "names": ["Nickel Metabolic Disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nickel Metabolic Disorder", "shortest_name_length": 25}
{"curie": "MONDO:0021071", "names": ["tumor larynx", "larynx tumor", "larynx tumors", "Larynx--Tumors", "LARYNGEAL TUMOR", "Tumor of larynx", "tumor of larynx", "neoplasm larynx", "Neoplasm larynx", "NEOPLASM LARYNX", "laryngeal tumor", "larynx neoplasm", "Larynx Neoplasm", "Larynx Neoplasms", "Tumour of larynx", "Neoplasm, Larynx", "neoplasms larynx", "Neoplasms, Larynx", "Neoplasm of Larynx", "neoplasm of larynx", "laryngeal neoplasm", "Laryngeal neoplasm", "LARYNGEAL NEOPLASM", "Neoplasm of larynx", "Laryngeal Neoplasm", "Neoplasm, Laryngeal", "Laryngeal neoplasia", "tumor of the larynx", "Laryngeal Neoplasms", "laryngeal neoplasia", "LARYNGEAL NEOPLASIA", "laryngeal neoplasms", "Neoplasms, Laryngeal", "neoplasm of the larynx", "Neoplasm of the larynx", "Laryngeal neoplasm NOS", "Neoplasm of the Larynx", "larynx neoplasm (disease)", "Neoplasm of larynx (disorder)", "neoplasm of larynx (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "laryngeal neoplasm", "shortest_name_length": 12}
{"curie": "UMLS:C0220630", "names": ["Liver Cancer", "Adult Liver Carcinoma", "Adult Primary Liver Cancer", "adult primary liver cancer", "Liver cancer, adult primary", "liver cancer, adult primary", "Adult Primary Liver Carcinoma", "Adult Primary Cancer of Liver", "Adult Primary Cancer of the Liver"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult Liver Carcinoma", "shortest_name_length": 12}
{"curie": "MONDO:0019682", "names": ["congenital sialidosis type 2"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital sialidosis type 2", "shortest_name_length": 28}
{"curie": "UMLS:C0042136", "names": ["uterus infection", "infection uterus", "UTERUS INFECTION", "infections uterus", "uterus; infection", "Uterine infection", "UTERINE INFECTION", "uterine infection", "infection; uterus", "infections uterine", "infection of uterus", "Infection of uterus", "Uterine infection NOS", "uterus; disorder, infective", "uterine infection (diagnosis)", "Infection of uterus (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infection of uterus", "shortest_name_length": 16}
{"curie": "UMLS:C1336191", "names": ["Stage IIB Osteosarcoma", "Stage IIB Osteogenic Sarcoma", "Stage IIB Osteosarcoma AJCC v7", "Stage IIB Osteosarcoma  AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIB Osteosarcoma AJCC v7", "shortest_name_length": 22}
{"curie": "UMLS:C4725020", "names": ["Moderate Hepatic Impairment", "Moderate Hepatic Insufficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Moderate Hepatic Insufficiency", "shortest_name_length": 27}
{"curie": "MONDO:0020764", "names": ["Brown-Pearce tumor", "Brown-Pearce carcinoma", "Brown-Pearce Carcinoma", "Carcinoma, Brown Pearce", "Carcinoma, Brown-Pearce", "carcinoma, Brown Pearce", "carcinoma, Brown-Pearce", "Brown-Pearce Epithelioma", "Brown-Pearce epithelioma", "Epithelioma, Brown Pearce", "Epithelioma, Brown-Pearce", "epithelioma, Brown Pearce", "epithelioma, Brown-Pearce"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Brown-Pearce carcinoma", "shortest_name_length": 18}
{"curie": "UMLS:C1333309", "names": ["Distantly Metastatic Malignant Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Distantly Metastatic Malignant Neoplasm", "shortest_name_length": 39}
{"curie": "UMLS:C5555848", "names": ["Metastatic Sarcoma in the Peritoneum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic Sarcoma in the Peritoneum", "shortest_name_length": 36}
{"curie": "MONDO:0020763", "names": ["MKHK1", "Menke-Hennekam syndrome 1", "MENKE-HENNEKAM SYNDROME 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Menke-Hennekam syndrome 1", "shortest_name_length": 5}
{"curie": "MONDO:0008624", "names": ["Upington disease", "UPINGTON DISEASE", "Familial dyschondroplasia", "familial dyschondroplasia", "hip dysplasia-enchondromata-ecchondroma syndrome", "Hip dysplasia-enchondromata-ecchondroma syndrome", "Hip dysplasia with enchondromata and ecchondroma syndrome", "PERTHES-LIKE HIP DISEASE, ENCHONDROMATA, AND ECCHONDROMATA", "Perthes-like hip disease, enchondromata, and ecchondromata", "Perthes-like hip disease, enchondromata, and Ecchondromata", "Hip dysplasia with enchondromata and ecchondroma syndrome (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Upington disease", "shortest_name_length": 16}
{"curie": "MONDO:0008600", "names": ["snap finger", "Trigger Digit", "TRIGGER THUMB", "thumb trigger", "Trigger thumb", "Trigger Thumb", "trigger thumb", "Clicking thumb", "trigger finger", "thumbs trigger", "Thumb, Trigger", "Digit, Trigger", "Trigger Thumbs", "TRIGGER FINGER", "Trigger Digits", "Trigger finger", "finger trigger", "snapping finger", "Digits, Trigger", "Snapping Finger", "fingers trigger", "Thumbs, Trigger", "finger; snapping", "Finger, Snapping", "snapping; finger", "finger triggered", "Snapping Fingers", "Fingers, Snapping", "Triggering of thumb", "trigger finger of thumb", "Snapping thumb syndrome", "Trigger Finger Disorder", "Flexor Tendon Entrapment", "Trigger thumb - acquired", "Tendon Entrapment, Flexor", "Flexor Tendon Entrapments", "Entrapment, Flexor Tendon", "Tendon Entrapments, Flexor", "Entrapments, Flexor Tendon", "Digital flexor tenosynovitis", "bilateral trigger thumb (type)", "recurrent trigger thumb (type)", "congenital trigger thumb (type)", "trigger thumb (physical finding)", "trigger finger (physical finding)", "Snapping thumb syndrome (disorder)", "Nodular tendinous disease of thumb", "trigger finger of thumb (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trigger thumb", "shortest_name_length": 11}
{"curie": "MONDO:0016903", "names": ["deletion 4q", "4q deletion", "monosomy 4q", "4q monosomy", "partial monosomy 4q", "chromosome 4q deletion", "Chromosome 4q- Syndrome", "partial deletion of chromosome 4q", "partial monosomy of chromosome 4q", "partial deletion of the long arm of chromosome 4", "partial monosomy of the long arm of chromosome 4", "partial deletion of the long arm of chromosome type 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial deletion of the long arm of chromosome 4", "shortest_name_length": 11}
{"curie": "MONDO:0054727", "names": ["SPGF23", "spermatogenic failure 23", "SPERMATOGENIC FAILURE 23"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spermatogenic failure 23", "shortest_name_length": 6}
{"curie": "UMLS:C0853848", "names": ["Infection in an immunocompromized host", "Infection in an immunocompromised host"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Infection in an immunocompromised host", "shortest_name_length": 38}
{"curie": "MONDO:0003300", "names": ["Appendix Leiomyoma", "appendix leiomyoma", "leiomyoma of appendix", "Leiomyoma of appendix", "Appendiceal leiomyoma", "appendiceal leiomyoma", "Appendiceal Leiomyoma", "Leiomyoma of Appendix", "Leiomyoma of the Appendix", "leiomyoma of the appendix", "vermiform appendix leiomyoma", "leiomyoma of vermiform appendix", "Leiomyoma of appendix (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "appendix leiomyoma", "shortest_name_length": 18}
{"curie": "MONDO:0017204", "names": ["toxic maculopathy due to antimalarial drugs"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "toxic maculopathy due to antimalarial drugs", "shortest_name_length": 43}
{"curie": "MONDO:0032843", "names": ["OPML1", "oculopharyngeal myopathy with leukoencephalopathy 1", "OCULOPHARYNGEAL MYOPATHY WITH LEUKOENCEPHALOPATHY 1"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "oculopharyngeal myopathy with leukoencephalopathy 1", "shortest_name_length": 5}
{"curie": "UMLS:C3854458", "names": ["Cerebral ventricular rupture"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cerebral ventricular rupture", "shortest_name_length": 28}
{"curie": "MONDO:0100063", "names": ["Pericytoma t(7;12)", "Pericytoma with t(7;12)", "pericytoma with t(7;12)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pericytoma with t(7;12)", "shortest_name_length": 18}
{"curie": "MONDO:0015760", "names": ["T-cell NHL", "T-cell lymphoma", "T cell lymphoma", "lymphoma t-cell", "lymphoma t cell", "T Cell Lymphoma", "T-Cell Lymphoma", "t cell lymphoma", "t-cell lymphoma", "cell lymphoma t", "LYMPHOMA T CELL", "lymphoma; T-cell", "Lymphoma, T-Cell", "T-Cell Lymphomas", "cell lymphomas t", "Lymphoma, T Cell", "cells lymphoma t", "T-cell; lymphoma", "Lymphoma, T-cell", "Lymphomas, T-Cell", "T-cell lymphoma NOS", "T-cell lymphoma (clinical)", "T-cell lymphoma (disorder)", "T-cell lymphoma (diagnosis)", "T-Cell Non-Hodgkin Lymphoma", "T-cell non-Hodgkin lymphoma", "Non-Hodgkin's T-Cell Lymphoma", "T-Cell Non-Hodgkin's Lymphoma", "non-Hodgkin's T-cell lymphoma", "T-cell non-Hodgkin's lymphoma", "Lymphomas non-Hodgkin's T-cell", "Malignant lymphoma, T-cell type", "Lymphoma, non-Hodgkin lymphoma, T-cell", "T-cell and NK-cell non-Hodgkin lymphoma", "T-Cell and NK-Cell Non-Hodgkin Lymphoma", "T-cell and NK-cell non-Hodgkin's lymphoma", "T-Cell and NK-Cell Non-Hodgkin's Lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "T-cell non-Hodgkin lymphoma", "shortest_name_length": 10}
{"curie": "UMLS:C1112261", "names": ["Gaze palsy", "gaze palsy", "Gaze palsies"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Gaze palsy", "shortest_name_length": 10}
{"curie": "MONDO:0008475", "names": ["Spondylistheses", "Spondylisthesis", "spondylisthesis", "Spondylolithesis", "Slipped backbone", "spondylolithesis", "Spondylolistheses", "spondylolistheses", "Spondylolisthesis", "SPONDYLOLISTHESIS", "spondylolisthesis", "Spondylolisthesis NOS", "Spondylolisthesis, NOS", "SPL - Spondylolisthesis", "spondylolisthesis (disease)", "Spondylolisthesis (disorder)", "Spondylolisthesis, site unspecified", "Displacement of one backbone compared to another"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "spondylolisthesis", "shortest_name_length": 15}
{"curie": "UMLS:C5670480", "names": ["Supratentorial Ependymoma, YAP1-MAMLD1 Fusion-Positive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Supratentorial Ependymoma, YAP1-MAMLD1 Fusion-Positive", "shortest_name_length": 54}
{"curie": "MONDO:0003987", "names": ["lung lymphoma", "Lung Lymphoma", "Lymphoma of Lung", "lymphoma of lung", "Pulmonary Lymphoma", "pulmonary Lymphoma", "pulmonary lymphoma", "lymphoma of the lung", "Lymphoma of the Lung", "Primary Lung Lymphoma", "primary lung lymphoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "lung lymphoma", "shortest_name_length": 13}
{"curie": "UMLS:C1513269", "names": ["Microcyst", "Microcysts", "Microcyst (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Microcyst", "shortest_name_length": 9}
{"curie": "MONDO:0005828", "names": ["Listerioses", "Listeriosis", "LISTERIOSIS", "listeriosis", "Listerellosis", "Listeriosis, NOS", "Circling disease", "listeria infection", "Listeria Infection", "Listeria infection", "Listeria Infections", "Infection, Listeria", "Listeria infections", "Infections, Listeria", "Listeriosis (disorder)", "listeriosis (diagnosis)", "Listeriosis, unspecified", "Infection caused by Listeria", "Listeria monocytogenes infection", "listeria monocytogenes infection", "infection; Listeria monocytogenes", "Listeria monocytogenes; infection", "listeriosis listeria monocytogenes", "infection by Listeria monocytogenes", "Infection by Listeria monocytogenes", "Infection caused by Listeria (disorder)", "Infection due to Listeria monocytogenes", "Listeria monocytogenes infectious disease", "Listeria monocytogenes disease or disorder", "Listeria monocytogenes infection (diagnosis)", "Listeria monocytogenes caused disease or disorder"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "listeriosis", "shortest_name_length": 11}
{"curie": "UMLS:C2346456", "names": ["III", "Stage III Multiple Myeloma", "Multiple Myeloma Stage III", "Stage III Plasma Cell Myeloma", "ISS Stage III Multiple Myeloma", "ISS Stage III Plasma Cell Myeloma", "ISS Stage III Multiple Myeloma/Plasma Cell Myeloma", "International Staging System Stage III Multiple Myeloma", "International Staging System Stage III Plasma Cell Myeloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ISS Stage III Plasma Cell Myeloma", "shortest_name_length": 3}
{"curie": "EFO:0011057", "names": ["neurotoxicity"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neurotoxicity", "shortest_name_length": 13}
{"curie": "MONDO:0017331", "names": ["Pilotto syndrome", "Pilotto syndrome (disorder)", "Cleft lip and palate, congenital heart disease, scoliosis, short stature, and mental retardation", "cleft lip and palate, congenital heart disease, scoliosis, short stature, and mental retardation", "cleft lip and palate, congenital heart disease, scoliosis, short stature, and intellectual disability"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Pilotto syndrome", "shortest_name_length": 16}
{"curie": "MONDO:0007887", "names": ["leiomyoma of vulva and esophagus", "LEIOMYOMA OF VULVA AND ESOPHAGUS", "Leiomyoma of vulva and esophagus", "esophagogastric and vulvar leiomyomatosis", "Esophagogastric and vulvar leiomyomatosis", "Leiomyomatosis, esophagogastric and vulvar", "leiomyomatosis, esophagogastric and vulvar", "LEIOMYOMATOSIS, ESOPHAGOGASTRIC AND VULVAR"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "leiomyoma of vulva and esophagus", "shortest_name_length": 32}
{"curie": "MONDO:0017113", "names": ["isolated bilateral hemispheric cerebellar hypoplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "isolated bilateral hemispheric cerebellar hypoplasia", "shortest_name_length": 52}
{"curie": "MONDO:0008824", "names": ["FADS", "FADS1", "Fetal akinesia", "Foetal akinesia", "PENA SHOKEIR SYNDROME", "pena shokeir syndrome", "Pena-Shokeir Syndrome", "Pena-Shokeir Phenotype", "Pena-Shokeir phenotype", "Fetal akinesia sequence", "fetal akinesia sequence", "FETAL AKINESIA SEQUENCE", "foetal akinesia sequence", "Foetal akinesia sequence", "Pena-Shokeir syndrome type I", "Pena-Shokeir syndrome type 1", "Pena Shokeir syndrome, type 1", "Pena-Shokeir syndrome, Type 1", "Pena-Shokeir Syndrome, Type I", "PENA-SHOKEIR SYNDROME, TYPE I", "Lethal Pena-Shokeir 1 syndrome", "FETAL AKINESIA DEFORMATION SEQUENCE", "fetal akinesia deformation sequence", "Fetal Akinesia Deformation Sequence", "Fetal akinesia-hypokinesia sequence", "Fetal akinesia deformation sequence", "Early severe fetal akinesia sequence", "Foetal akinesia-hypokinesia sequence", "FETAL AKINESIA DEFORMATION SEQUENCE 1", "Early severe foetal akinesia sequence", "Pena-Shokeir syndrome type I (disorder)", "fetal akinesia deformation sequence syndrome", "foetal akinesia deformation sequence syndrome", "Arthrogryposis multiplex congenita pulmonary hypoplasia", "ARTHROGRYPOSIS MULTIPLEX CONGENITA WITH PULMONARY HYPOPLASIA", "Arthrogryposis multiplex congenita with pulmonary hypoplasia", "arthrogryposis multiplex congenita with pulmonary hypoplasia", "Arthrogryposis multiplex congenita-pulmonary hypoplasia syndrome", "arthrogryposis multiplex congenita-pulmonary hypoplasia syndrome", "Arthrogryposis multiplex congenita, pulmonary hypoplasia, cryptorchidism, and unusual ophthalmological findings"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "fetal akinesia deformation sequence", "shortest_name_length": 4}
{"curie": "MONDO:0023062", "names": ["encephalocele anencephaly"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephalocele anencephaly", "shortest_name_length": 25}
{"curie": "MONDO:0004600", "names": ["Leukemia monocytic", "leukemia monocytic", "monocytic leukemia", "Monocytic Leukemia", "LEUKEMIA MONOCYTIC", "Monocytic leukemia", "Monocytoid leukemia", "Monocytic leukaemia", "LEUKAEMIA MONOCYTIC", "Leukaemia monocytic", "monocytic; leukemia", "MONOCYTIC LEUKEMIAS", "monocytic leukaemia", "Monocytic leukemias", "monocytoid leukemia", "leukemia; monocytic", "LEUKEMIA, MONOCYTIC", "Monocytic Leukemias", "Monoblastic leukemia", "schilling's leukemia", "Schilling's leukemia", "histiocytic leukemia", "Monocytic leukaemias", "Histiocytic leukemia", "LEUKEMIA, HISTIOCYTIC", "histiocytic; leukemia", "Monoblastic leukaemia", "Schilling's leukaemia", "leukemia; histiocytic", "monoblastic; leukemia", "LEUKEMIA, MONOBLASTIC", "Histiocytic leukaemia", "leukemia; monoblastic", "Monocytic leukemia NOS", "[M]Monocytic leukemias", "Leukemia monocytic NOS", "[M]Monocytic leukaemias", "Monocytic leukemia, NOS", "Leukaemia monocytic NOS", "Monocytic leukaemia NOS", "Monocytic leukaemia, NOS", "Other monocytic leukemia", "Monoblastic leukemia, NOS", "Other monocytic leukaemia", "Other monocytic leukemia NOS", "Monocytic leukemia (disorder)", "Unspecified monocytic leukemia", "monocytic leukemia (diagnosis)", "Unspecified monocytic leukaemia", "Monocytic leukemia, unspecified", "Monocytic leukaemia, unspecified", "Schilling-type monocytic leukemia", "Schilling-type monocytic leukaemia", "Monocytic leukemia, unspecified NOS", "Monocytic leukemia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "monocytic leukemia", "shortest_name_length": 18}
{"curie": "MONDO:0000983", "names": ["Flasher", "flasher", "flashers", "exhibitionism", "Exhibitionism", "exhibitionist", "Exhibitionist", "Exhibitionisms", "exhibitionists", "Exhibitionism (disorder)", "exhibitionism (diagnosis)", "deviation; sexual, exhibitionism", "sexual; deviation, exhibitionism"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "exhibitionism", "shortest_name_length": 7}
{"curie": "UMLS:C5420532", "names": ["Unresectable Cervical Adenosquamous Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Unresectable Cervical Adenosquamous Carcinoma", "shortest_name_length": 45}
{"curie": "MONDO:0002734", "names": ["Anal Colloid Adenocarcinoma", "anal colloid adenocarcinoma", "anal mucinous adenocarcinoma", "Anal Mucinous Adenocarcinoma", "anus mucinous adenocarcinoma", "anal colloidal adenocarcinoma", "Anal Colloidal Adenocarcinoma", "Colloid Adenocarcinoma of Anus", "colloid adenocarcinoma of anus", "Mucinous Adenocarcinoma of Anus", "mucinous adenocarcinoma of anus", "Colloidal Adenocarcinoma of Anus", "colloidal adenocarcinoma of anus", "Colloid Adenocarcinoma of the Anus", "colloid adenocarcinoma of the anus", "Mucinous Adenocarcinoma of the Anus", "mucinous adenocarcinoma of the anus", "Colloidal Adenocarcinoma of the Anus", "colloidal adenocarcinoma of the anus", "mucinous adenocarcinoma of anus (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anal mucinous adenocarcinoma", "shortest_name_length": 27}
{"curie": "MONDO:0002259", "names": ["gonad disease", "gonad disorder", "GONAD DISORDER", "gonadal disease", "gonadal disorder", "Gonadal Disorder", "Disease of gonad", "disease of gonad", "disorders gonads", "Gonads--Diseases", "Disorder, Gonadal", "gonadal disorders", "Gonadal Disorders", "disorder of gonad", "Disorders, Gonadal", "Disorder of Gonads", "disorder of gonads", "Gonadal dysfunction", "Gonadal Dysfunction", "GONADAL DYSFUNCTION", "gonad disease or disorder", "disease or disorder of gonad"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "gonadal disorder", "shortest_name_length": 13}
{"curie": "MONDO:0000225", "names": ["HME", "Ehrlichia chaffeensis", "Ehrlichiosis chafeensis", "ehrlichiosis chafeensis", "ehrlichiosis chaffeensis", "human monocytic ehrlichiosis", "ehrlichiosis chaffeensis (diagnosis)", "Ehrlichiosis chafeensis [E. chafeensis]", "Human ehrlichiosis due to Ehrlichia chaffeensis", "human ehrlichiosis due to Ehrlichia chaffeensis", "Human ehrlichial infection, human monocytic type", "human ehrlichiosis caused by Ehrlichia chaffeensis", "Human ehrlichiosis caused by Ehrlichia chaffeensis", "Human ehrlichiosis caused by Ehrlichia chaffeensis (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "human monocytic ehrlichiosis", "shortest_name_length": 3}
{"curie": "MONDO:0007036", "names": ["Achard Syndrome", "Achard syndrome", "ACHARD SYNDROME", "Dysostoses and increased ligament laxity", "arachnodactyly, receding lower jaw and joint laxity of hands/feet", "Arachnodactyly, receding lower jaw, and joint laxity limited to the hands and feet"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Achard syndrome", "shortest_name_length": 15}
{"curie": "UMLS:C0752198", "names": ["Adult-Onset Idiopathic Focal Dystonias", "Adult Onset Idiopathic Focal Dystonias"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Adult-Onset Idiopathic Focal Dystonias", "shortest_name_length": 38}
{"curie": "MONDO:0000682", "names": ["time agnosia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "time agnosia", "shortest_name_length": 12}
{"curie": "MONDO:0006617", "names": ["bullous dermatoses", "dermatoses, bullous", "bullous skin disease", "bullous skin diseases", "skin disease, bullous", "vesicular skin disease", "skin diseases, bullous", "vesicular skin diseases", "skin disease, vesicular", "skin diseases, vesicular", "Sneddon Wilkinson disease", "Sneddon-Wilkinson disease", "vesiculobullous dermatoses", "Vesiculobullous Dermatoses", "Vesiculobullous dermatosis", "Dermatoses, Vesiculobullous", "dermatoses, vesiculobullous", "vesiculobullous skin disease", "Vesiculobullous Skin Disease", "vesiculobullous skin diseases", "Skin Disease, Vesiculobullous", "Vesiculobullous Skin Diseases", "skin disease, vesiculobullous", "subcorneal pustular dermatoses", "subcorneal pustular dermatosis", "Skin Diseases, Vesiculobullous", "Vesiculobullous disease of skin", "dermatosis, subcorneal pustular", "pustular dermatosis, subcorneal", "pustular dermatoses, subcorneal", "dermatoses, subcorneal pustular"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "vesiculobullous skin disease", "shortest_name_length": 18}
{"curie": "UMLS:C1332512", "names": ["Benign Mediastinal Hemangiopericytoma", "Benign Hemangiopericytoma of Mediastinum", "Benign Hemangiopericytoma of the Mediastinum"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Benign Mediastinal Hemangiopericytoma", "shortest_name_length": 37}
{"curie": "MONDO:0003354", "names": ["Heart Sarcoma", "heart sarcoma", "sarcoma heart", "HEART, SARCOMA", "Cardiac sarcoma", "Cardiac Sarcoma", "cardiac sarcoma", "sarcoma of heart", "Sarcoma of Heart", "sarcoma of Heart", "sarcoma of the heart", "Sarcoma of the Heart", "CARDIAC CANCER, SARCOMA"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "heart sarcoma", "shortest_name_length": 13}
{"curie": "UMLS:C4330593", "names": ["Lumbosacral Spinal Cord Ependymal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Lumbosacral Spinal Cord Ependymal Tumor", "shortest_name_length": 39}
{"curie": "MONDO:0011054", "names": ["PAPPAS", "Autosomal recessive amelia", "autosomal recessive amelia", "Amelia, Autosomal Recessive", "amelia, autosomal recessive", "AMELIA, AUTOSOMAL RECESSIVE", "Autosomal recessive amelia (disorder)", "Amelia, posterior, with pelvic and pulmonary hypoplasia syndrome", "AMELIA, POSTERIOR, WITH PELVIC AND PULMONARY HYPOPLASIA SYNDROME"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive amelia", "shortest_name_length": 6}
{"curie": "MONDO:0100077", "names": ["CAD", "congenital alveolar dysplasia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "congenital alveolar dysplasia", "shortest_name_length": 3}
{"curie": "MONDO:0015695", "names": ["combined immunodeficiency due to CRAC channel dysfunction", "Combined immunodeficiency due to CRAC channel dysfunction", "Immune dysfunction with T-cell inactivation due to calcium entry defect", "immune dysfunction due to T-cell inactivation due to calcium entry defect", "Immune dysfunction due to T-cell inactivation due to calcium entry defect", "Combined immunodeficiency due to calcium release activated calcium channel dysfunction", "Combined immunodeficiency due to CRAC (calcium release activated calcium) channel dysfunction", "Combined immunodeficiency due to calcium release activated calcium channel dysfunction (disorder)", "Combined immunodeficiency due to calcium release activated calcium channel dysfunction (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "combined immunodeficiency due to CRAC channel dysfunction", "shortest_name_length": 57}
{"curie": "MONDO:0019276", "names": ["inherited epidermolysis bullosa", "hereditary epidermolysis bullosa", "epidermolysis bullosa hereditaria"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "inherited epidermolysis bullosa", "shortest_name_length": 31}
{"curie": "MONDO:0003820", "names": ["mature teratoma", "ovary mature teratoma", "mature ovarian teratoma", "ovarian mature teratoma", "Mature Ovarian Teratoma", "mature teratoma, ovarian", "mature teratoma of ovary", "Mature Teratoma of Ovary", "teratoma, mature, ovarian", "Mature Teratoma of the Ovary", "mature teratoma of the ovary"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mature ovarian teratoma", "shortest_name_length": 15}
{"curie": "UMLS:C0233750", "names": ["Hysterical Amnesia", "hysterical amnesia", "Hysterical amnesia", "hysterical; amnesia", "amnesia; hysterical", "Amnesia, Hysterical", "Hysterical Amnesias", "Amnesias, Hysterical"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Hysterical amnesia", "shortest_name_length": 18}
{"curie": "MONDO:0001487", "names": ["Ca intrahepatic bile ducts", "intrahepatic gall duct cancer", "intrahepatic bile duct cancer", "Intrahepatic bile duct cancer", "cancer of intrahepatic bile duct", "Intrahepatic bile duct cancer NOS", "malignant tumor of intrahepatic bile duct", "malignant intrahepatic bile duct neoplasm", "malignant neoplasm of intrahepatic gall duct", "Malignant neoplasm of intrahepatic gall duct", "malignant neoplasm of intrahepatic bile duct", "Malignant neoplasm of intrahepatic bile ducts", "malignant neoplasm of intrahepatic bile ducts", "malignant neoplasm of intrahepatic biliary passages", "Malignant neoplasm of intrahepatic biliary passages", "Malignant neoplasm of intrahepatic gall duct (disorder)", "malignant neoplasm of intrahepatic bile duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "intrahepatic bile duct cancer", "shortest_name_length": 26}
{"curie": "MONDO:0014478", "names": ["MRMV3", "MIRROR MOVEMENTS 3", "mirror movements 3", "mirror movements type 3", "DNAL4 familial congenital mirror movements", "familial congenital mirror movements caused by mutation in DNAL4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "mirror movements 3", "shortest_name_length": 5}
{"curie": "MONDO:0012021", "names": ["MYP17", "myopia 4", "MYP4, FORMERLY", "myopia 4, formerly", "MYOPIA 4, FORMERLY", "MYOPIA 17, AUTOSOMAL DOMINANT", "myopia 17, autosomal dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "myopia 17, autosomal dominant", "shortest_name_length": 5}
{"curie": "UMLS:C0751119", "names": ["Symptomatic Tonic Clonic Epilepsy", "Symptomatic Tonic-Clonic Epilepsy", "Tonic-Clonic Epilepsy, Symptomatic", "Epilepsy, Symptomatic Tonic-Clonic", "Epilepsy, Tonic-Clonic, Symptomatic", "Symptomatic Tonic-Clonic Epilepsies", "Tonic-Clonic Epilepsies, Symptomatic", "Epilepsies, Symptomatic Tonic-Clonic"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Epilepsy, Tonic-Clonic, Symptomatic", "shortest_name_length": 33}
{"curie": "UMLS:C3899982", "names": ["BCLC Stage 0 Hepatocellular Cancer", "BCLC Stage 0 Hepatocellular Carcinoma", "Barcelona Clinic Liver Cancer Stage 0 Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "BCLC Stage 0 Hepatocellular Carcinoma", "shortest_name_length": 34}
{"curie": "MONDO:0024344", "names": ["Pityriasis folliculorum", "pityriasis folliculorum", "Pityriasis folliculorum (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pityriasis folliculorum", "shortest_name_length": 23}
{"curie": "UMLS:C0457523", "names": ["COD", "Cementoma", "Cementoma, NOS", "Osseous Dysplasia", "Cemental Dysplasia", "cemento-osseous dysplasia", "Cemento osseous dysplasia", "Cemento-Osseous Dysplasia", "Cemento-osseous dysplasia", "Cemento-osseous dysplasia (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Cemento-osseous dysplasia", "shortest_name_length": 3}
{"curie": "MONDO:0022963", "names": ["DIA", "Desmoplastic infantile astrocytoma", "Desmoplastic Infantile Astrocytoma", "desmoplastic infantile astrocytoma", "Desmoplastic Astrocytoma of Infancy", "Desmoplastic astrocytoma of infancy", "Desmoplastic infantile astrocytoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "desmoplastic infantile astrocytoma", "shortest_name_length": 3}
{"curie": "MONDO:0010006", "names": ["Sandhoff", "O variant", "Sandhoff disease", "sandhoff disease", "Sandhoff Disease", "SANDHOFF DISEASE", "Sandhoffs Disease", "sandhoffs disease", "Sandhoff's disease", "Sandhoff's Disease", "sandhoff's disease", "Adult Sandhoff Disease", "SANDHOFF DISEASE, ADULT", "Sandhoff Disease, Adult", "Juvenile Sandhoff Disease", "GM2-gangliosidosis, type 2", "GM2 Gangliosidosis, Type 2", "Type II GM2-Gangliosidoses", "Sandhoff Disease, Juvenile", "gangliosidosis GM2 type II", "Infantile Sandhoff Disease", "GM2 gangliosidosis, type 2", "Type II GM2-Gangliosidosis", "GM2-Gangliosidosis, Type II", "Gangliosidosis GM2, Type II", "Sandhoff disease (disorder)", "Sandhoff Jatzkewitz disease", "Sandhoff Disease, Infantile", "GM2 gangliosidosis, type II", "GM2-Gangliosidoses, Type II", "GM2 Gangliosidosis, Type II", "SANDHOFF DISEASE, INFANTILE", "GM2-GANGLIOSIDOSIS, TYPE II", "Sandhoff disease, adult type", "Sandhoff Disease, Adult Type", "GM>2< gangliosidosis, type 2", "SANDHOFF DISEASE, ADULT TYPE", "GM2 gangliosidosis 0 variant", "Sandhoff disease (diagnosis)", "Sandhoff disease, adult form", "Gangliosidosis G(M2), Type II", "G(M2) Gangliosidosis, Type II", "GM2 gangliosidosis, 0 variant", "total hexosaminidase deficiency", "Sandhoff disease, juvenile form", "Sandhoff disease, juvenile type", "Sandhoff Disease, Juvenile Type", "Total hexosaminidase deficiency", "SANDHOFF DISEASE, JUVENILE TYPE", "Sandhoff-Jatzkewitz-Pilz disease", "Sandhoff Disease, Infantile Type", "SANDHOFF DISEASE, INFANTILE TYPE", "Sandhoff-Jatzkewitz-Pilz Disease", "Sandhoff disease, infantile type", "Sandhoff Jatzkewitz Pilz Disease", "Sandhoff disease, infantile form", "Hexosaminidase A and B deficiency", "Hexosaminidase A AND B deficiency", "hexosaminidase a and b deficiency", "Disease, Sandhoff-Jatzkewitz-Pilz", "Hexosaminidases A and B deficiency", "Adult GM2 gangliosidosis 0 variant", "Hexosaminidases a and B deficiency", "HEXOSAMINIDASES A AND B DEFICIENCY", "Hexosaminidases A And B Deficiency", "GM<sub>2</sub> gangliosidosis, type 2", "Juvenile GM2 gangliosidosis 0 variant", "Infantile GM2 gangliosidosis 0 variant", "hexosaminidase A and B deficiency disease", "Hexosaminidase A and B Deficiency Disease", "Deficiency Disease, Hexosaminidase A and B", "Beta-hexosaminidase-beta-subunit deficiency", "Hexosaminidases A and B deficiency, adult form", "Hexosaminidases A and B deficiency, juvenile form", "Hexosaminidases A and B deficiency, infantile form", "Sandhoff disease, infantile, juvenile, and adult forms"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Sandhoff disease", "shortest_name_length": 8}
{"curie": "MONDO:0013370", "names": ["LQT6", "LQT6 syndrome", "LQT3/6, DIGENIC", "LONG QT SYNDROME 6", "Long Qt Syndrome 6", "long QT syndrome 6", "KCNE2 long QT syndrome", "long QT syndrome type 6", "LQT6 syndrome (diagnosis)", "LONG QT SYNDROME 3/6, DIGENIC", "long QT syndrome 3/6, digenic", "LONG QT SYNDROME 3/6, DIGENIC Disorder", "long QT syndrome caused by mutation in KCNE2", "long QT syndrome 6, acquired, susceptibility to", "LONG QT SYNDROME 6, ACQUIRED, SUSCEPTIBILITY TO"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "long QT syndrome 6", "shortest_name_length": 4}
{"curie": "MONDO:0012099", "names": ["ATIC DEFICIENCY", "ATIC deficiency", "Atic deficiency", "AICA-ribosiduria", "AICA-RIBOSURIA DUE TO ATIC DEFICIENCY", "Aica-Ribosuria due to Atic deficiency", "AICA Ribosuria due to ATIC Deficiency", "AICA-RIBOSIDURIA DUE TO ATIC DEFICIENCY", "AICA-ribosiduria due to ATIC deficiency", "5-amino-4-imidazole carboxamide ribosiduria", "AICAR TRANSFORMYLASE/IMP CYCLOHYDROLASE DEFICIENCY", "AICA (5-amino-4-imidazole carboxamide) ribosiduria", "AICAR transformylase/IMP cyclohydrolase deficiency", "5-amino-4-imidazole carboxamide ribosiduria (disorder)", "5-amino-4-imidazole carboxamide ribosiduria (diagnosis)", "AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency", "disorders of purine metabolism 5-amino-4-imidazole carboxamide ribosiduria", "ATIC (5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/imp cyclohydrolase) deficiency"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "AICA-ribosiduria", "shortest_name_length": 15}
{"curie": "MONDO:0017611", "names": ["pituitary tumor", "Pituitary Tumor", "Pituitary tumor", "PITUITARY TUMOR", "tumor, pituitary", "Pituitary Tumors", "pituitary tumour", "pituitary tumors", "Tumor, Pituitary", "Pituitary tumour", "Tumors, Pituitary", "pituitary tumours", "Pituitary Neoplasm", "PITUITARY NEOPLASM", "tumor of pituitary", "Tumor of Pituitary", "pituitary neoplasm", "pituitary neoplasms", "Pituitary tumor NOS", "Neoplasm, Pituitary", "Pituitary Neoplasms", "Pituitary neoplasms", "Neoplasms, Pituitary", "Pituitary tumour NOS", "pituitary gland tumor", "Pituitary Gland Tumor", "neoplasm of pituitary", "Neoplasm of Pituitary", "pituitary gland tumour", "Pituitary neoplasm NOS", "tumor of the pituitary", "PITUITARY NEOPLASM NOS", "Tumour;pituitary gland", "Tumor of the Pituitary", "Pituitary gland--Tumors", "tumor of pituitary gland", "Pituitary gland neoplasm", "Pituitary Gland Neoplasm", "Tumor of pituitary gland", "Tumor of Pituitary Gland", "pituitary gland neoplasm", "Tumour of pituitary gland", "neoplasm of the pituitary", "Neoplasm of the Pituitary", "Neoplasm of Pituitary Gland", "neoplasm of pituitary gland", "Neoplasm of pituitary gland", "Tumor of the Pituitary Gland", "tumor of the pituitary gland", "Neoplasm of the pituitary gland", "Neoplasm of the Pituitary Gland", "neoplasm of the pituitary gland", "Neoplasm of pituitary gland (disorder)", "neoplasm of pituitary gland (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pituitary tumor", "shortest_name_length": 15}
{"curie": "UMLS:C0521174", "names": ["Microcalcinoses", "Microcalcinosis", "microcalcification", "Microcalcification", "Microcalcifications", "microcalcifications", "Microcalcification, calcified structure", "Microcalcification, calcified structure (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Microcalcification", "shortest_name_length": 15}
{"curie": "UMLS:C4330006", "names": ["Fourth Ventricle Ependymal Tumor"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Fourth Ventricle Ependymal Tumor", "shortest_name_length": 32}
{"curie": "MONDO:0010121", "names": ["TAR", "Tar syndrome", "tAR syndrome", "TAR syndrome", "syndrome tar", "TAR Syndrome", "tar syndrome", "TAR SYNDROME", "syndrome; TAR", "syndrome tars", "TAR; syndrome", "Thrombocytopenia Absent Radii", "thrombocytopenia absent radii", "Absent radii and thrombocytopenia", "absent radii and thrombocytopenia", "absence; radius in thrombocytopenia", "chromosome 1q21.1 deletion syndrome", "thrombocytopenia; with absent radius", "thrombocytopenia-absent radii syndrome", "Thrombocytopenia-absent radii syndrome", "thrombocytopenia absent radius syndrome", "Thrombocytopenia-absent radius syndrome", "Thrombocytopenia absent radius syndrome", "thrombocytopenia-absent radius syndrome", "Thrombocytopenia-Absent Radius Syndrome", "THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME", "Radial Aplasia-Thrombocytopenia Syndrome", "radial aplasia-thrombocytopenia syndrome", "Radial aplasia-thrombocytopenia syndrome", "thrombocytopenia; absent radius, syndrome", "chromosome 1Q21.1 deletion syndrome, 200-Kb", "Chromosome 1q21.1 Deletion Syndrome, 200-Kb", "CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB", "thrombocytopenia with absent radius syndrome", "Thrombocytopenia with absent radius syndrome", "syndrome; thrombocytopenia with absent radius", "Radial Aplasia-Amegakaryocytic Thrombocytopenia", "Thrombocytopenia with absent radii (TAR) syndrome", "thrombocytopenia with absent radii (TAR) syndrome", "Thrombocytopenia with absent radius [TAR] syndrome", "TAR - Thrombocytopenia with absent radius syndrome", "Radial aplasia-thrombocytopenia syndrome (disorder)", "thrombocytopenia with absent radius syndrome (diagnosis)", "1q21.1 susceptibility locus for Thrombocytopenia-Absent Radius (TAR) syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "thrombocytopenia-absent radius syndrome", "shortest_name_length": 3}
{"curie": "UMLS:C5239315", "names": ["Platinum-Resistant Malignant Female Reproductive System Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Platinum-Resistant Malignant Female Reproductive System Neoplasm", "shortest_name_length": 64}
{"curie": "UMLS:C0428993", "names": ["ATRIAL TRIGEMINY", "Atrial trigeminy", "Atrial Trigeminy", "Atrial trigeminy (disorder)", "Atrial Trigeminy by ECG Finding", "Atrial Trigeminy by EKG Finding"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Atrial trigeminy", "shortest_name_length": 16}
{"curie": "UMLS:C4553574", "names": ["Stage III Renal Pelvis and Ureter Cancer", "stage III renal pelvis and ureter cancer AJCC v8", "Stage III Renal Pelvis and Ureter Cancer AJCC v8", "stage III renal pelvis and ureter urothelial carcinoma AJCC v8", "Stage III Renal Pelvis and Ureter Urothelial Carcinoma AJCC v8", "stage III transitional cell cancer of the renal pelvis and ureter"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Renal Pelvis and Ureter Cancer AJCC v8", "shortest_name_length": 40}
{"curie": "MONDO:0012386", "names": ["trichoscyphodysplasia", "TRICHOSCYPHODYSPLASIA", "Trichoscyphodysplasia", "metaphyseal chondrodysplasia with ectodermal dysplasia", "METAPHYSEAL CHONDRODYSPLASIA WITH ECTODERMAL DYSPLASIA", "Metaphyseal chondrodysplasia with ectodermal dysplasia", "cupped metaphyses and cone-Shaped epiphyses with alopecia", "Cupped metaphyses and cone-shaped epiphyses with alopecia", "CUPPED METAPHYSES AND CONE-SHAPED EPIPHYSES WITH ALOPECIA", "Metaphyseal chondrodysplasia with cone-shaped epiphyses and alopecia", "METAPHYSEAL CHONDRODYSPLASIA WITH CONE-SHAPED EPIPHYSES AND ALOPECIA", "metaphyseal chondrodysplasia with cone-Shaped epiphyses and alopecia"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "trichoscyphodysplasia", "shortest_name_length": 21}
{"curie": "MONDO:0100406", "names": ["AML, inv(16)(p13q24)", "AML, inv(16)(p13;q24)", "AML, inv(16)(p13.3q24.3)", "AML, inv(16)(p13.3;q24.3)", "acute myeloid leukemia, inv(16)(p13.3;q24.3)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, inv(16)(p13.3;q24.3)", "shortest_name_length": 20}
{"curie": "MONDO:0020562", "names": ["PLS", "PLLS", "pleomorphic liposarcoma", "Pleomorphic liposarcoma", "Pleomorphic Liposarcoma", "Liposarcoma, Pleomorphic", "Pleomorphic Liposarcomas", "liposarcoma; pleomorphic", "pleomorphic; liposarcoma", "Pleomorphic liposarcoma (disorder)", "pleomorphic liposarcoma (diagnosis)", "pleomorphic liposarcoma (morphologic abnormality)", "Pleomorphic liposarcoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pleomorphic liposarcoma", "shortest_name_length": 3}
{"curie": "MONDO:0012236", "names": ["KTCN4", "keratoconus 4", "KERATOCONUS 4", "Keratoconus 4"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "keratoconus 4", "shortest_name_length": 5}
{"curie": "MONDO:0000997", "names": ["monocular esotropia", "esotropia monocular", "Monocular esotropia", "Monocular Esotropia", "ESOTROPIA MONOCULAR", "Esotropia, monocular", "Esotropia, Monocular", "Monocular Esotropias", "Monocular esotropia, NOS", "Monocular esotropia (disorder)", "monocular esotropia (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "monocular esotropia", "shortest_name_length": 19}
{"curie": "MONDO:0016964", "names": ["trisomy 14q", "14q trisomy", "Duplication 14q", "14q duplication", "partial trisomy 14q", "chromosome 14q duplication", "partial trisomy of chromosome 14q", "partial duplication of chromosome 14q", "partial trisomy of the long arm of chromosome 14", "partial duplication of the long arm of chromosome 14", "partial duplication of the long arm of chromosome type 14"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "partial duplication of the long arm of chromosome 14", "shortest_name_length": 11}
{"curie": "MONDO:0007314", "names": ["Abdominal chemodectomas with cutaneous angiolipomas", "abdominal chemodectomas with cutaneous angiolipomas", "chemodectoma, intraabdominal, with cutaneous angiolipomas", "CHEMODECTOMA, INTRAABDOMINAL, WITH CUTANEOUS ANGIOLIPOMAS", "Chemodectoma, Intraabdominal, with Cutaneous Angiolipomas", "Familial abdominal chemodectomas with cutaneous angiolipomas"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "chemodectoma, intraabdominal, with cutaneous angiolipomas", "shortest_name_length": 51}
{"curie": "MONDO:0003810", "names": ["bladder diffuse clear cell adenocarcinoma", "Bladder Diffuse Clear Cell Adenocarcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "bladder diffuse clear cell adenocarcinoma", "shortest_name_length": 41}
{"curie": "MONDO:0009163", "names": ["encephalomalacia, multilocular", "ENCEPHALOMALACIA, MULTILOCULAR", "Encephalomalacia, Multilocular"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "encephalomalacia, multilocular", "shortest_name_length": 30}
{"curie": "UMLS:C3898705", "names": ["Intracranial Laceration Related to Birth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Intracranial Laceration Related to Birth", "shortest_name_length": 40}
{"curie": "MONDO:0003320", "names": ["Blastema Predominant Wilms Tumor", "blastema predominant Wilms tumor", "blastema predominant Wilms' tumor", "Wilms tumor, blastema predominant", "blastema predominant Wilm's tumor", "Wilms' tumor, blastema predominant", "Wilm's tumor, blastema predominant", "blastema predominant nephroblastoma", "Blastema Predominant Nephroblastoma", "Blastema Predominant renal Wilms tumor", "blastema predominant renal Wilms tumor", "Blastema Predominant Renal Wilms Tumor", "blastema predominant renal Wilm's tumor", "Blastema Predominant Kidney Wilms Tumor", "blastema predominant renal Wilms' tumor", "Blastema Predominant Renal Wilms' Tumor", "blastema predominant kidney Wilms tumor", "Blastema Predominant renal Wilms tumour", "Blastema Predominant Renal Adenosarcoma", "blastema predominant renal adenosarcoma", "Blastema Predominant Renal Wilm's Tumor", "blastema predominant kidney Wilms' tumor", "blastema predominant kidney adenosarcoma", "Blastema Predominant Kidney Adenosarcoma", "blastema predominant kidney Wilms' tumour"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "blastema predominant kidney Wilms tumor", "shortest_name_length": 32}
{"curie": "UMLS:C4682640", "names": ["Stage IVA Primary Peritoneal Cancer", "Stage IVA Primary Peritoneal Cancer AJCC v8", "Stage IVA Primary Peritoneal Carcinoma AJCC v8"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IVA Primary Peritoneal Cancer AJCC v8", "shortest_name_length": 35}
{"curie": "MONDO:0006260", "names": ["renal medulla carcinoma", "Renal Medullary Carcinoma", "Renal medullary carcinoma", "renal medullary carcinoma", "carcinoma of renal medulla", "Kidney Medullary Carcinoma", "kidney medullary carcinoma", "Renal medullary carcinoma (disorder)", "Renal medullary carcinoma (diagnosis)", "Renal medullary carcinoma (morphologic abnormality)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "kidney medullary carcinoma", "shortest_name_length": 23}
{"curie": "MONDO:0007704", "names": ["OS2", "HOA", "Dipoa", "OADIP", "HEBERDEN NODE", "heberden node", "Heberden node", "node; Heberden", "HEBERDEN NODES", "heberden nodes", "Heberden; node", "heberdens node", "Heberden nodes", "Heberden's node", "Heberden's Node", "heberdens nodes", "heberden's node", "Heberdens nodes", "heberden's nodes", "Heberden's nodes", "Hand osteoarthritis", "hand osteoarthritis", "HAND OSTEOARTHRITIS", "osteoarthritis hand", "MATN3 osteoarthritis", "hands osteoarthritis", "osteoarthritis of hand", "osteoarthrosis of hand", "Osteoarthrosis of hand", "Tuberculum Arthriticum", "Heberden node (disorder)", "Osteoarthritis of the hand", "Heberden's nodes were seen", "Osteoarthritis - hand joint", "DISTAL INTERPHALANGEAL NODULE", "OSTEOARTHRITIS SUSCEPTIBILITY 2", "osteoarthritis susceptibility 2", "Degenerative joint disease of hand", "osteoarthrosis of hand (diagnosis)", "osteoarthritis of hand (diagnosis)", "Heberden's nodes (physical finding)", "osteoarthritis susceptibility type 2", "Heberden's nodes (painless nodules DIP)", "osteoarthritis caused by mutation in MATN3", "Degenerative joint disease of hand (disorder)", "osteoarthritis of distal interphalangeal joints", "painless nodule on distal interphalangeal (DIP) joint"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "osteoarthritis susceptibility 2", "shortest_name_length": 3}
{"curie": "UMLS:C3146262", "names": ["Stage III Prostate Cancer", "Stage III Prostate Cancer AJCC v7"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage III Prostate Cancer AJCC v7", "shortest_name_length": 25}
{"curie": "MONDO:0009459", "names": ["CIP", "HSAN2D", "HSAN2D, AR", "ASYMBOLIA FOR PAIN", "Asymbolia for Pain", "asymbolia for pain", "channelopathy-associated CIP", "Congenital Pain Insensitivity", "Congenital Insensitivity to Pain", "insensitivity to pain, congenital", "CONGENITAL ANALGESIA, AUTOSOMAL RECESSIVE", "Congenital Analgesia, Autosomal Recessive", "congenital analgesia, autosomal recessive", "insensitivity to pain, channelopathy-associated", "Insensitivity to Pain, Channelopathy-Associated", "INSENSITIVITY TO PAIN, CHANNELOPATHY-ASSOCIATED", "neuropathy, hereditary sensory and autonomic, type 2D", "INDIFFERENCE TO PAIN, CONGENITAL, AUTOSOMAL RECESSIVE", "Indifference to Pain, Congenital, Autosomal Recessive", "indifference to pain, congenital, autosomal recessive", "NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IID", "neuropathy, hereditary sensory and autonomic, type IID", "channelopathy-associated congenital insensitivity to pain, autosomal recessive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "channelopathy-associated congenital insensitivity to pain, autosomal recessive", "shortest_name_length": 3}
{"curie": "UMLS:C5238472", "names": ["Advanced Hepatocellular Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Advanced Hepatocellular Carcinoma", "shortest_name_length": 33}
{"curie": "MONDO:0002283", "names": ["NAD", "NBIA2A", "Axonal Dystrophy", "Axonal dystrophy", "DYSTROPHY, AXONAL", "Neuroaxonal dystrophy", "neuroaxonal dystrophy", "Neuroaxonal Dystrophy", "Dystrophy, Neuroaxonal", "Neuroaxonal Dystrophies", "Neuroaxonal dystrophy (disorder)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "neuroaxonal dystrophy", "shortest_name_length": 3}
{"curie": "MONDO:0015613", "names": ["DD", "dentin dysplasia", "Dentin Dysplasia", "Dentin dysplasia", "Dysplasia, Dentin", "dentin; dysplasia", "dysplasia; dentin", "Dentin Dysplasias", "Dentine dysplasia", "dentinal dysplasia", "Dysplasias, Dentin", "Dentinal dysplasia", "Dentin dysplasia (disorder)", "dentinal dysplasia (diagnosis)", "Dentinogenesis imperfecta of baby teeth", "Dentinogenesis imperfecta limited to primary teeth"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "dentin dysplasia", "shortest_name_length": 2}
{"curie": "MONDO:0004506", "names": ["Peripheral Breast Papilloma", "Breast Peripheral Papilloma", "peripheral breast papilloma", "Microscopic Breast Papilloma", "microscopic breast papilloma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "microscopic breast papilloma", "shortest_name_length": 27}
{"curie": "UMLS:C1336205", "names": ["stage IIIA endometrial cancer", "Stage IIIA Uterine Corpus Cancer", "stage IIIA endometrial carcinoma", "stage IIIA uterine corpus cancer", "Stage IIIA Uterine Corpus Cancer AJCC v7", "stage IIIA uterine corpus cancer AJCC v7", "Stage IIIA Uterine (including Endometrial) Cancer"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Stage IIIA Uterine Corpus Cancer AJCC v7", "shortest_name_length": 29}
{"curie": "MONDO:0007434", "names": ["PFE", "DENTAL NONERUPTION", "dental noneruption", "Dental Noneruption", "Primary retention of teeth", "Primary Retention of Teeth", "primary retention of teeth", "PRIMARY RETENTION OF TEETH", "Retention of primary teeth", "Posterior Openbite, Familial", "unerupted second primary molar", "Unerupted Second Primary Molar", "UNERUPTED SECOND PRIMARY MOLAR", "primary failure of tooth eruption", "Primary failure of tooth eruption", "failure of tooth eruption, primary", "Failure of Tooth Eruption, Primary", "FAILURE OF TOOTH ERUPTION, PRIMARY", "Failure of eruption of primary teeth", "PFE - primary failure of tooth eruption", "nonsyndromic primary failure of eruption", "familial posterior openbite malocclusion", "primary failure of eruption, nonsyndromic", "POSTERIOR OPENBITE MALOCCLUSION, FAMILIAL", "posterior Openbite malocclusion, familial", "Primary Failure of Eruption, Nonsyndromic", "Primary failure of tooth eruption (disorder)", "PRIMARY FAILURE OF TOOTH ERUPTION, NONSYNDROMIC"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "primary failure of tooth eruption", "shortest_name_length": 3}
{"curie": "MONDO:0014092", "names": ["SCZD18", "schizophrenia 18", "SCHIZOPHRENIA 18", "schizophrenia type 18", "schizoaffective disorder", "schizophrenia susceptibility 18", "Chromosome 7q36.3 Duplication Syndrome, 362-Kb", "chromosome 7q36.3 Duplication syndrome, 362-Kb", "schizophrenia 18 with or without an affective disorder", "SCHIZOPHRENIA 18 WITH OR WITHOUT AN AFFECTIVE DISORDER"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "schizophrenia 18", "shortest_name_length": 6}
{"curie": "MONDO:0008333", "names": ["Incomplete Pseudoxanthoma Elasticum", "Pseudoxanthoma Elasticum, Incomplete", "Incomplete Pseudoxanthoma Elasticums", "Elasticum, Incomplete Pseudoxanthoma", "Elasticums, Incomplete Pseudoxanthoma", "Pseudoxanthoma Elasticums, Incomplete", "PSEUDOXANTHOMA ELASTICUM, FORME FRUSTE", "PSEUDOXANTHOMA ELASTICUM, HETEROZYGOUS", "pseudoxanthoma elasticum, heterozygous", "Pseudoxanthoma Elasticum, Forme Fruste", "pseudoxanthoma elasticum, forme fruste", "Pseudoxanthoma Elasticum, Heterozygous", "Pseudoxanthoma Elasticum, Autosomal Dominant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "pseudoxanthoma elasticum, forme fruste", "shortest_name_length": 35}
{"curie": "UMLS:C2111716", "names": ["Extrahepatic Bile Duct Large Cell NEC", "Extrahepatic Bile Duct Large Cell Neuroendocrine Carcinoma", "large cell neuroendocrine carcinoma of extrahepatic bile duct", "large cell neuroendocrine carcinoma of extrahepatic bile duct (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "large cell neuroendocrine carcinoma of extrahepatic bile duct", "shortest_name_length": 37}
{"curie": "MONDO:0001156", "names": ["BPD", "Borderline personality", "BORDERLINE PERSONALITY", "borderline personality", "borderline personalities", "Borderline Personality Disorder", "borderline personality disorder", "Borderline personality disorder", "personality disorder; borderline", "Personality Disorder, Borderline", "Disorder, Borderline Personality", "borderline; personality disorder", "Borderline Personality Disorders", "borderline personality disorders", "Disorders, Borderline Personality", "Personality Disorders, Borderline", "BPD - borderline personality disorder", "borderline personality disorder (disease)", "Borderline personality disorder (disorder)", "borderline personality disorder (diagnosis)"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "borderline personality disorder", "shortest_name_length": 3}
{"curie": "UMLS:C5556720", "names": ["Metastatic HER2-Positive Breast Carcinoma", "Metastatic HER2 Positive Breast Carcinoma"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Metastatic HER2-Positive Breast Carcinoma", "shortest_name_length": 41}
{"curie": "UMLS:C1333561", "names": ["FIGO Stage IVB GTT", "FIGO Stage IVB Gestational Trophoblastic Tumor", "FIGO Stage IVB Gestational Trophoblastic Neoplasm"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "FIGO Stage IVB Gestational Trophoblastic Tumor", "shortest_name_length": 18}
{"curie": "MONDO:0019732", "names": ["ALys amyloidosis", "lysozyme amyloidosis", "familial renal amyloidosis due to lysozyme variant", "hereditary renal amyloidosis due to lysozyme variant", "familial amyloid nephropathy due to lysozyme variant", "hereditary amyloid nephropathy due to lysozyme variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "ALys amyloidosis", "shortest_name_length": 16}
{"curie": "MONDO:0009577", "names": ["MMR syndrome", "MMR SYNDROME", "Neuhauser syndrome", "NEUHAUSER SYNDROME", "Neuhäuser syndrome", "NeuhC$user syndrome", "Megalocornea-Mental Retardation Syndrome", "megalocornea mental retardation syndrome", "MEGALOCORNEA-MENTAL RETARDATION SYNDROME", "megalocornea-mental retardation syndrome", "Megalocornea mental retardation syndrome", "megalocornea intellectual disability syndrome", "Megalocornea-intellectual disability syndrome", "megalocornea-intellectual disability syndrome", "megalocornea-mental retardation (MMR) syndrome", "MMR (megalocornea, mental retardation) syndrome", "megalocornea with intellectual disability syndrome", "Megalocornea with intellectual disability syndrome", "Cerebral palsy-hypotonic seizures-megalcornea syndrome", "cerebral palsy-hypotonic seizures-megalcornea syndrome", "megalocornea-developmental retardation-dysmorphic syndrome", "Megalocornea with intellectual disability syndrome (disorder)", "megalocornea with intellectual disability syndrome (diagnosis)", "megalocornea-macrocephaly-mental and motor retardation syndrome", "Megalocornea-macrocephaly-mental and motor retardation (MMMM) syndrome", "megalocornea-macrocephaly-mental and motor retardation (MMMM) syndrome", "Seizures-hypotonic cerebral palsy-megalocornea-mental retardation syndrome", "seizures-hypotonic cerebral palsy-megalocornea-mental retardation syndrome"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "megalocornea-intellectual disability syndrome", "shortest_name_length": 12}
{"curie": "MONDO:0012418", "names": ["DFNB62", "autosomal recessive deafness 62", "DEAFNESS, AUTOSOMAL RECESSIVE 62", "deafness, autosomal recessive 62", "Deafness, Autosomal Recessive 62", "autosomal recessive nonsyndromic deafness 62", "autosomal recessive nonsyndromic hearing loss 62", "autosomal recessive nonsyndromic deafness type 62"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "autosomal recessive nonsyndromic hearing loss 62", "shortest_name_length": 6}
{"curie": "MONDO:0011078", "names": ["Jung Wolff back Stahl syndrome", "Jung Wolff Back Stahl syndrome", "ANTERIOR CHAMBER CLEAVAGE DISORDER, CEREBELLAR HYPOPLASIA, HYPOTHYROIDISM, AND TRACHEAL STENOSIS", "Anterior chamber cleavage disorder, cerebellar hypoplasia, hypothyroidism, and tracheal stenosis", "anterior chamber cleavage disorder, cerebellar hypoplasia, hypothyroidism, and tracheal stenosis"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "anterior chamber cleavage disorder, cerebellar hypoplasia, hypothyroidism, and tracheal stenosis", "shortest_name_length": 30}
{"curie": "MONDO:0012082", "names": ["ASPG1", "ASPERGER syndrome, susceptibility to, 1", "asperger syndrome, susceptibility to, 1", "ASPERGER SYNDROME, SUSCEPTIBILITY TO, 1", "Asperger syndrome susceptibility 1, Isolated cases"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "asperger syndrome, susceptibility to, 1", "shortest_name_length": 5}
{"curie": "MONDO:0008366", "names": ["RED CELL PERMEABILITY DEFECT", "red cell permeability defect", "ELLIPTOCYTOSIS WITH TRANSVERSE SLITLIKE CHANGES", "elliptocytosis with transverse slitlike changes"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "red cell permeability defect", "shortest_name_length": 28}
{"curie": "MONDO:0007357", "names": ["COLONIC VARICES WITHOUT PORTAL HYPERTENSION", "Colonic Varices without Portal Hypertension", "colonic varices without portal hypertension"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "colonic varices without portal hypertension", "shortest_name_length": 43}
{"curie": "MONDO:0100405", "names": ["AML, Non-MLL MLLT10 Rearrangement", "AML, Non-KMT2A MLLT10 Rearrangement", "AML, Non-MLL MLLT10 Rearrangement Positive", "AML, Non-KMT2A MLLT10 rearrangement positive", "acute myeloid leukemia, Non-KMT2A MLLT10 rearrangement positive"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "acute myeloid leukemia, Non-KMT2A MLLT10 rearrangement positive", "shortest_name_length": 33}
{"curie": "UMLS:C5235045", "names": ["Hodgkin disease, nodular sclerosis, syncytial variant", "Nodular Sclerosis Hodgkin Lymphoma, Syncytial Variant", "Hodgkin's Disease, Nodular Sclerosis, Syncytial Variant", "Nodular Sclerosis Classic Hodgkin Lymphoma, Syncytial Variant", "Nodular Sclerosis Classical Hodgkin Lymphoma, Syncytial Variant"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Nodular Sclerosis Classic Hodgkin Lymphoma, Syncytial Variant", "shortest_name_length": 53}
{"curie": "MONDO:0030033", "names": ["SENEBAC", "seizures, early-onset, with neurodegeneration and brain calcification", "SEIZURES, EARLY-ONSET, WITH NEURODEGENERATION AND BRAIN CALCIFICATIONS", "seizures, early-onset, with neurodegeneration and brain calcifications"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "seizures, early-onset, with neurodegeneration and brain calcifications", "shortest_name_length": 7}
{"curie": "MESH:D004195", "names": ["Disease Models, Animal"], "types": ["Disease", "DiseaseOrPhenotypicFeature", "BiologicalEntity", "ThingWithTaxon", "NamedThing", "Entity"], "preferred_name": "Disease Models, Animal", "shortest_name_length": 22}